Genotype ID	Sex	MP ID	MP Term	Allelic Composition	Background Strain	Sex-specific Normal Y/N	Citation (PubMed/MGI)
MGI:2167486	F	MP:0008871	abnormal ovarian follicle number	Kit<W-42J>/Kit<+>	C57BL/6J-Kit<W-42J>/J	N	7274658
MGI:2167486	M	MP:0001147	small testis	Kit<W-42J>/Kit<+>	C57BL/6J-Kit<W-42J>/J	N	7274658
MGI:2168183	M	MP:0003415	priapism	Ada<tm1Mw>/Ada<tm1Mw>	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	18340377
MGI:2168183	M	MP:0001379	abnormal penile erection	Ada<tm1Mw>/Ada<tm1Mw>	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	18340377
MGI:2169746	F	MP:0001923	reduced female fertility	Mafb<kr>/Mafb<kr>	Not Specified	N	MGI:63176
MGI:2169746	M	MP:0001922	reduced male fertility	Mafb<kr>/Mafb<kr>	Not Specified	N	MGI:63176
MGI:2170665	M	MP:0011410	ectopic testis	Foxc1<ch>/Foxc1<ch>	involves: C57BL/6 * CHMU/Le	N	10704385
MGI:2170665	F	MP:0011797	blind ureter	Foxc1<ch>/Foxc1<ch>	involves: C57BL/6 * CHMU/Le	N	10704385
MGI:2170665	F	MP:0011727	ectopic ovary	Foxc1<ch>/Foxc1<ch>	involves: C57BL/6 * CHMU/Le	N	10704385
MGI:2170665	M	MP:0011486	ectopic ureter	Foxc1<ch>/Foxc1<ch>	involves: C57BL/6 * CHMU/Le	N	10704385
MGI:2170796	F	MP:0001927	abnormal estrous cycle	Dbf/Dbf<+>	involves: 101/H * C3H/HeH	N	9062079
MGI:2170796	F	MP:0001926	female infertility	Dbf/Dbf<+>	involves: 101/H * C3H/HeH	N	9062079
MGI:2170796	M	MP:0001925	male infertility	Dbf/Dbf<+>	involves: 101/H * C3H/HeH	N	9062079
MGI:2170796	M	MP:0004852	decreased testis weight	Dbf/Dbf<+>	involves: 101/H * C3H/HeH	N	MGI:62405
MGI:2170796	M	MP:0004852	decreased testis weight	Dbf/Dbf<+>	involves: 101/H * C3H/HeH	N	9062079
MGI:2170796	M	MP:0002687	oligozoospermia	Dbf/Dbf<+>	involves: 101/H * C3H/HeH	N	9062079
MGI:2171276	M	MP:0002660	abnormal caput epididymis morphology	Kit<W>/Kit<W-v>	Not Specified	N	32499443
MGI:2172319	M	MP:0002769	abnormal vas deferens morphology	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>,Hoxd11<tm1Mrc>/Hoxd11<tm1Mrc>	mixed	N	7596412
MGI:2173283	F	MP:0014270	decreased ovary secretion	Gsx1<tm1Ssp>/Gsx1<tm1Ssp>	involves: 129P2/OlaHsd	N	8631293
MGI:2173283	M	MP:0014269	decreased testes secretion	Gsx1<tm1Ssp>/Gsx1<tm1Ssp>	involves: 129P2/OlaHsd	N	8631293
MGI:2173367	F	MP:0013721	abnormal mammary placode morphology	Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>	involves: 129P2/OlaHsd * C57BL/6	N	16720875
MGI:2173367	F	MP:0013785	abnormal mammary gland bud morphology	Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>	involves: 129P2/OlaHsd * C57BL/6	N	11782400
MGI:2173367	F	MP:0000629	absent mammary gland	Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>	involves: 129P2/OlaHsd * C57BL/6	N	11782400
MGI:2174716	F	MP:0001926	female infertility	Aff1<Rob>/Aff1<+>	involves: BALB/cAnNCrl * C3H/HeN	N	12629167
MGI:2174716	M	MP:0001922	reduced male fertility	Aff1<Rob>/Aff1<+>	involves: BALB/cAnNCrl * C3H/HeN	N	12629167
MGI:2174744	F	MP:0001926	female infertility	Scarb1<tm1Kri>/Scarb1<tm1Kri>	involves: 129S2/SvPas * C57BL/6	N	25368174
MGI:2174744	F	MP:0003982	increased cholesterol level	Scarb1<tm1Kri>/Scarb1<tm1Kri>	involves: 129S2/SvPas * C57BL/6	N	25368174
MGI:2174744	F	MP:0003191	abnormal cellular cholesterol metabolism	Scarb1<tm1Kri>/Scarb1<tm1Kri>	involves: 129S2/SvPas * C57BL/6	N	25368174
MGI:2174744	F	MP:0031013	abnormal egg activation	Scarb1<tm1Kri>/Scarb1<tm1Kri>	involves: 129S2/SvPas * C57BL/6	N	25368174
MGI:2174744	F	MP:0001926	female infertility	Scarb1<tm1Kri>/Scarb1<tm1Kri>	involves: 129S2/SvPas * C57BL/6	N	10430941
MGI:2174744	F	MP:0005168	abnormal female meiosis	Scarb1<tm1Kri>/Scarb1<tm1Kri>	involves: 129S2/SvPas * C57BL/6	N	25368174
MGI:2174744	F	MP:0001125	abnormal oocyte morphology	Scarb1<tm1Kri>/Scarb1<tm1Kri>	involves: 129S2/SvPas * C57BL/6	N	10430941
MGI:2174744	F	MP:0009093	oocyte degeneration	Scarb1<tm1Kri>/Scarb1<tm1Kri>	involves: 129S2/SvPas * C57BL/6	N	25368174
MGI:2174744	F	MP:0000242	impaired fertilization	Scarb1<tm1Kri>/Scarb1<tm1Kri>	involves: 129S2/SvPas * C57BL/6	N	25368174
MGI:2174744	F	MP:0001926	female infertility	Scarb1<tm1Kri>/Scarb1<tm1Kri>	involves: 129S2/SvPas * C57BL/6	N	11733567
MGI:2174749	F	MP:0001510	abnormal coat appearance	Strg/Strg<+>	involves: BALB/c * C3H/HeN	N	10932191
MGI:2174766	M	MP:0003205	testicular atrophy	Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * SJL	N	17360455
MGI:2174766	F	MP:0001125	abnormal oocyte morphology	Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * SJL	N	15084742
MGI:2174766	M	MP:0006379	abnormal spermatocyte morphology	Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * SJL	N	15084742
MGI:2174766	M	MP:0014052	increased male germ cell apoptosis	Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * SJL	N	15084742
MGI:2174766	M	MP:0014052	increased male germ cell apoptosis	Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * SJL	N	17360455
MGI:2174766	F	MP:0005168	abnormal female meiosis	Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * SJL	N	15084742
MGI:2174766	M	MP:0005169	abnormal male meiosis	Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * SJL	N	15084742
MGI:2174766	F	MP:0001923	reduced female fertility	Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * SJL	N	15084742
MGI:2174785	F	MP:0003578	absent ovary	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	N	12368184
MGI:2174785	F	MP:0003320	rectovaginal fistula	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	N	12368184
MGI:2174785	F	MP:0001140	abnormal vagina epithelium morphology	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	N	10227294
MGI:2174785	F	MP:0001119	abnormal female reproductive system morphology	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	N	12368184
MGI:2174785	M	MP:0001159	absent prostate gland	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	N	11106548
MGI:2174785	F	MP:0000629	absent mammary gland	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	N	10227294
MGI:2174785	F	MP:0003575	absent oviduct	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	N	12368184
MGI:2174785	M	MP:0009736	abnormal prostate gland branching morphogenesis	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	N	11106548
MGI:2174785	F	MP:0009101	clitoris hypoplasia	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	N	12368184
MGI:2174785	F	MP:0001137	abnormal uterine cervix epithelium morphology	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	N	10227294
MGI:2174786	F	MP:0001926	female infertility	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	N	10716451
MGI:2174786	M	MP:0001380	reduced male mating frequency	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	N	10716451
MGI:2174791	F	MP:0001926	female infertility	Ttpa<tm1Far>/Ttpa<tm1Far>	involves: 129S4/SvJae * C57BL/6	N	11095717
MGI:2174799	M	MP:0004851	increased testis weight	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	10746634
MGI:2174799	F	MP:0001923	reduced female fertility	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	11385068
MGI:2174799	M	MP:0001156	abnormal spermatogenesis	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	10746634
MGI:2174799	F	MP:0001132	absent mature ovarian follicles	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	9241280
MGI:2174799	F	MP:0001121	uterus hypoplasia	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	9241280
MGI:2174799	F	MP:0001926	female infertility	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	9241280
MGI:2174799	F	MP:0001926	female infertility	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	11385068
MGI:2174799	M	MP:0001145	abnormal male reproductive system morphology	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	10746634
MGI:2174799	M	MP:0001925	male infertility	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	9241280
MGI:2174799	M	MP:0001925	male infertility	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	11385068
MGI:2174799	M	MP:0002675	asthenozoospermia	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	10746634
MGI:2174799	F	MP:0001927	abnormal estrous cycle	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	10746634
MGI:2174799	M	MP:0002687	oligozoospermia	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	10746634
MGI:2174799	M	MP:0001922	reduced male fertility	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	11385068
MGI:2174799	F	MP:0001119	abnormal female reproductive system morphology	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	9241280
MGI:2174799	M	MP:0009257	dilated seminiferous tubule	Vdr<tm1Ska>/Vdr<tm1Ska>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	10746634
MGI:2174808	F	MP:0001926	female infertility	Wnt7a<px>/Wnt7a<px>	involves: STOCK Sox18<Ra>	N	MGI:48652
MGI:2174808	M	MP:0001925	male infertility	Wnt7a<px>/Wnt7a<px>	involves: STOCK Sox18<Ra>	N	MGI:48652
MGI:2174809	F	MP:0008257	thin myometrium	Wnt7a<tm1Amc>/Wnt7a<tm1Amc>	involves: 129S1/Sv	N	9790192
MGI:2174809	F	MP:0009081	thin uterus	Wnt7a<tm1Amc>/Wnt7a<tm1Amc>	involves: 129S1/Sv	N	9790192
MGI:2174809	F	MP:0009097	absent endometrial glands	Wnt7a<tm1Amc>/Wnt7a<tm1Amc>	involves: 129S1/Sv	N	9790192
MGI:2174809	F	MP:0002637	small uterus	Wnt7a<tm1Amc>/Wnt7a<tm1Amc>	involves: 129S1/Sv	N	9790192
MGI:2174809	F	MP:0001120	abnormal uterus morphology	Wnt7a<tm1Amc>/Wnt7a<tm1Amc>	involves: 129S1/Sv	N	9790192
MGI:2174809	F	MP:0003572	abnormal uterus development	Wnt7a<tm1Amc>/Wnt7a<tm1Amc>	involves: 129S1/Sv	N	9790192
MGI:2174809	F	MP:0003574	abnormal oviduct morphology	Wnt7a<tm1Amc>/Wnt7a<tm1Amc>	involves: 129S1/Sv	N	9790192
MGI:2174809	F	MP:0009071	short oviduct	Wnt7a<tm1Amc>/Wnt7a<tm1Amc>	involves: 129S1/Sv	N	9790192
MGI:2174809	F	MP:0001926	female infertility	Wnt7a<tm1Amc>/Wnt7a<tm1Amc>	involves: 129S1/Sv	N	9790192
MGI:2174809	M	MP:0001925	male infertility	Wnt7a<tm1Amc>/Wnt7a<tm1Amc>	involves: 129S1/Sv	N	9790192
MGI:2174817	M	MP:0000649	sebaceous gland atrophy	Tg(APOC1)3Lmh/Y	C57BL/6-Tg(APOC1)3Lmh	N	9421476
MGI:2174817	M	MP:0001554	increased circulating free fatty acids level	Tg(APOC1)3Lmh/Y	C57BL/6-Tg(APOC1)3Lmh	N	9421476
MGI:2174817	M	MP:0003853	dry skin	Tg(APOC1)3Lmh/Y	C57BL/6-Tg(APOC1)3Lmh	N	9421476
MGI:2174817	M	MP:0010072	increased pruritus	Tg(APOC1)3Lmh/Y	C57BL/6-Tg(APOC1)3Lmh	N	9421476
MGI:2174817	M	MP:0005145	increased circulating VLDL cholesterol level	Tg(APOC1)3Lmh/Y	C57BL/6-Tg(APOC1)3Lmh	N	9421476
MGI:2174817	M	MP:0000414	alopecia	Tg(APOC1)3Lmh/Y	C57BL/6-Tg(APOC1)3Lmh	N	9421476
MGI:2174817	M	MP:0005178	increased circulating cholesterol level	Tg(APOC1)3Lmh/Y	C57BL/6-Tg(APOC1)3Lmh	N	9421476
MGI:2174817	M	MP:0002092	abnormal eye morphology	Tg(APOC1)3Lmh/Y	C57BL/6-Tg(APOC1)3Lmh	N	9421476
MGI:2174817	M	MP:0001200	thick skin	Tg(APOC1)3Lmh/Y	C57BL/6-Tg(APOC1)3Lmh	N	9421476
MGI:2174817	M	MP:0001192	scaly skin	Tg(APOC1)3Lmh/Y	C57BL/6-Tg(APOC1)3Lmh	N	9421476
MGI:2174817	M	MP:0003975	increased circulating VLDL triglyceride level	Tg(APOC1)3Lmh/Y	C57BL/6-Tg(APOC1)3Lmh	N	9421476
MGI:2174817	M	MP:0001552	increased circulating triglyceride level	Tg(APOC1)3Lmh/Y	C57BL/6-Tg(APOC1)3Lmh	N	9421476
MGI:2174845	M	MP:0001147	small testis	Tg(Fst)10Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174846	F	MP:0001127	small ovary	Tg(Fst)4Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174846	F	MP:0001129	impaired ovarian folliculogenesis	Tg(Fst)4Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174846	F	MP:0001926	female infertility	Tg(Fst)4Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174846	F	MP:0001121	uterus hypoplasia	Tg(Fst)4Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174846	M	MP:0001147	small testis	Tg(Fst)4Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174847	M	MP:0001147	small testis	Tg(Fst)5Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174847	M	MP:0001154	seminiferous tubule degeneration	Tg(Fst)5Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174847	M	MP:0001155	arrest of spermatogenesis	Tg(Fst)5Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174847	M	MP:0001925	male infertility	Tg(Fst)5Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174847	M	MP:0001152	increased Leydig cell number	Tg(Fst)5Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174848	M	MP:0001147	small testis	Tg(Fst)7Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174849	M	MP:0001925	male infertility	Tg(Fst)9Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174849	M	MP:0001154	seminiferous tubule degeneration	Tg(Fst)9Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174849	F	MP:0001129	impaired ovarian folliculogenesis	Tg(Fst)9Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174849	M	MP:0001155	arrest of spermatogenesis	Tg(Fst)9Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174849	F	MP:0001121	uterus hypoplasia	Tg(Fst)9Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174849	M	MP:0001152	increased Leydig cell number	Tg(Fst)9Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174849	F	MP:0001127	small ovary	Tg(Fst)9Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174849	F	MP:0001926	female infertility	Tg(Fst)9Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174849	M	MP:0001147	small testis	Tg(Fst)9Zuk/0	involves: C3H * C57BL/6 * ICR	N	9440814
MGI:2174881	F	MP:0001882	abnormal lactation	Tg(rv-CYCLIN)29Dlh/0	involves: C57BL/6 * SJL	N	10811912
MGI:2174882	M	MP:0001151	enlarged foreskin	Tg(Tgfa)1Efu/0	Not Specified	N	1709129
MGI:2174882	F	MP:0001141	thickened vaginal epithelium	Tg(Tgfa)1Efu/0	Not Specified	N	1709129
MGI:2174882	M	MP:0001150	enlarged scrotum	Tg(Tgfa)1Efu/0	Not Specified	N	1709129
MGI:2174885	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(Wnt1)1Hev/0	either: FVB/N or (involves: C57BL/6 * SJL)	N	3180222
MGI:2174885	F	MP:0009505	abnormal mammary gland lobule morphology	Tg(Wnt1)1Hev/0	either: FVB/N or (involves: C57BL/6 * SJL)	N	3180222
MGI:2174885	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(Wnt1)1Hev/0	either: FVB/N or (involves: C57BL/6 * SJL)	N	3180222
MGI:2174885	F	MP:0000627	abnormal mammary gland morphology	Tg(Wnt1)1Hev/0	either: FVB/N or (involves: C57BL/6 * SJL)	N	3180222
MGI:2174895	M	MP:0006380	abnormal spermatid morphology	Six5<tm1Rdd>/Six5<tm1Rdd>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174895	M	MP:0001925	male infertility	Six5<tm1Rdd>/Six5<tm1Rdd>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174895	M	MP:0001156	abnormal spermatogenesis	Six5<tm1Rdd>/Six5<tm1Rdd>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174895	M	MP:0001146	abnormal testis morphology	Six5<tm1Rdd>/Six5<tm1Rdd>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174895	M	MP:0001147	small testis	Six5<tm1Rdd>/Six5<tm1Rdd>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174895	M	MP:0001932	abnormal spermiogenesis	Six5<tm1Rdd>/Six5<tm1Rdd>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174895	M	MP:0005250	decreased Sertoli cell number	Six5<tm1Rdd>/Six5<tm1Rdd>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174895	M	MP:0001154	seminiferous tubule degeneration	Six5<tm1Rdd>/Six5<tm1Rdd>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174895	M	MP:0005159	azoospermia	Six5<tm1Rdd>/Six5<tm1Rdd>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174895	M	MP:0001153	small seminiferous tubules	Six5<tm1Rdd>/Six5<tm1Rdd>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174895	M	MP:0001152	increased Leydig cell number	Six5<tm1Rdd>/Six5<tm1Rdd>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174897	M	MP:0002687	oligozoospermia	Six5<tm1Rdd>/Six5<+>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174897	M	MP:0001154	seminiferous tubule degeneration	Six5<tm1Rdd>/Six5<+>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174897	M	MP:0001146	abnormal testis morphology	Six5<tm1Rdd>/Six5<+>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174897	M	MP:0001153	small seminiferous tubules	Six5<tm1Rdd>/Six5<+>	129S4/SvJae-Six5<tm1Rdd>	N	15163633
MGI:2174939	M	MP:0002687	oligozoospermia	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	N	10490638
MGI:2174939	M	MP:0001145	abnormal male reproductive system morphology	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	N	10490638
MGI:2174939	F	MP:0002679	abnormal corpus luteum morphology	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	N	10490638
MGI:2174939	M	MP:0001153	small seminiferous tubules	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	N	10490638
MGI:2174939	M	MP:0001147	small testis	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	N	10490638
MGI:2174939	M	MP:0001146	abnormal testis morphology	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	N	10490638
MGI:2174939	F	MP:0001119	abnormal female reproductive system morphology	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	N	10490638
MGI:2174939	F	MP:0001926	female infertility	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	N	10490638
MGI:2174939	F	MP:0003356	impaired luteinization	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	N	10490638
MGI:2174939	M	MP:0001922	reduced male fertility	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	N	10490638
MGI:2174951	F	MP:0001923	reduced female fertility	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	9861029
MGI:2174951	F	MP:0002680	decreased corpora lutea number	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	9861029
MGI:2174951	F	MP:0031422	failure of superovulation	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	9861029
MGI:2174951	F	MP:0009372	abnormal cumulus oophorus morphology	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	9861029
MGI:2174951	F	MP:0001129	impaired ovarian folliculogenesis	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	9861029
MGI:2174951	M	MP:0001167	prostate gland epithelial hyperplasia	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	9861029
MGI:2174951	F	MP:0031239	increased atretic ovarian follicle number	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	9861029
MGI:2174951	F	MP:0009648	abnormal superovulation	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	9861029
MGI:2174951	F	MP:0031420	decreased superovulation rate	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	9861029
MGI:2174951	M	MP:0002566	abnormal sexual interaction	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11114183
MGI:2174975	F	MP:0003355	decreased ovulation rate	Nos1<tm1Plh>/Nos1<tm1Plh>	involves: 129S4/SvJae * C57BL/6	N	9848082
MGI:2174975	F	MP:0031420	decreased superovulation rate	Nos1<tm1Plh>/Nos1<tm1Plh>	involves: 129S4/SvJae * C57BL/6	N	9848082
MGI:2174977	M	MP:0006308	enlarged seminiferous tubules	Nos2<tm1Lau>/Nos2<tm1Lau>	involves: 129P2/OlaHsd * C57BL/6	N	12810565
MGI:2174977	M	MP:0001146	abnormal testis morphology	Nos2<tm1Lau>/Nos2<tm1Lau>	involves: 129P2/OlaHsd * C57BL/6	N	12810565
MGI:2174977	M	MP:0005169	abnormal male meiosis	Nos2<tm1Lau>/Nos2<tm1Lau>	involves: 129P2/OlaHsd * C57BL/6	N	12810565
MGI:2174977	M	MP:0004851	increased testis weight	Nos2<tm1Lau>/Nos2<tm1Lau>	involves: 129P2/OlaHsd * C57BL/6	N	12810565
MGI:2174977	M	MP:0030603	increased sperm number	Nos2<tm1Lau>/Nos2<tm1Lau>	involves: 129P2/OlaHsd * C57BL/6	N	12810565
MGI:2174979	M	MP:0001379	abnormal penile erection	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae	N	11904450
MGI:2174979	M	MP:0001378	abnormal ejaculation	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae	N	10549894
MGI:2175035	M	MP:0001153	small seminiferous tubules	Fyn<tm1Yik>/Fyn<tm1Yik>	involves: C57BL/6 * CBA	N	11751285
MGI:2175035	F	MP:0001486	abnormal startle reflex	Fyn<tm1Yik>/Fyn<tm1Yik>	involves: C57BL/6 * CBA	N	11834300
MGI:2175035	M	MP:0002216	abnormal seminiferous tubule morphology	Fyn<tm1Yik>/Fyn<tm1Yik>	involves: C57BL/6 * CBA	N	11751285
MGI:2175035	M	MP:0002687	oligozoospermia	Fyn<tm1Yik>/Fyn<tm1Yik>	involves: C57BL/6 * CBA	N	11751285
MGI:2175035	M	MP:0004852	decreased testis weight	Fyn<tm1Yik>/Fyn<tm1Yik>	involves: C57BL/6 * CBA	N	11751285
MGI:2175035	F	MP:0001906	increased dopamine level	Fyn<tm1Yik>/Fyn<tm1Yik>	involves: C57BL/6 * CBA	N	11834300
MGI:2175035	F	MP:0001386	abnormal maternal nurturing	Fyn<tm1Yik>/Fyn<tm1Yik>	involves: C57BL/6 * CBA	N	15154672
MGI:2175035	F	MP:0003459	increased fear-related response	Fyn<tm1Yik>/Fyn<tm1Yik>	involves: C57BL/6 * CBA	N	11834300
MGI:2175035	F	MP:0001384	abnormal pup retrieval	Fyn<tm1Yik>/Fyn<tm1Yik>	involves: C57BL/6 * CBA	N	15154672
MGI:2175035	M	MP:0031389	abnormal ectoplasmic specialization morphology	Fyn<tm1Yik>/Fyn<tm1Yik>	involves: C57BL/6 * CBA	N	11751285
MGI:2175038	F	MP:0001132	absent mature ovarian follicles	Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	8849725
MGI:2175038	F	MP:0001134	absent corpus luteum	Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	8849725
MGI:2175038	F	MP:0001126	abnormal ovary morphology	Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	8849725
MGI:2175038	F	MP:0001926	female infertility	Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	8849725
MGI:2175038	F	MP:0002016	ovary cyst	Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	8849725
MGI:2175038	F	MP:0001931	abnormal oogenesis	Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	8849725
MGI:2175038	F	MP:0001127	small ovary	Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	8849725
MGI:2175038	F	MP:0001130	abnormal ovarian folliculogenesis	Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	8849725
MGI:2175046	M	MP:0001922	reduced male fertility	Grin1<tm1Bhk>/Grin1<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	10481908
MGI:2175046	M	MP:0001380	reduced male mating frequency	Grin1<tm1Bhk>/Grin1<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	10481908
MGI:2175061	F	MP:0001577	anemia	Heph<Sla>/Heph<Sla>	involves: BALB/c * C3H	N	10932191
MGI:2175099	F	MP:0000629	absent mammary gland	Lef1<tm1Rug>/Lef1<tm1Rug>	involves: 129S2/SvPas * C57BL/6	N	7958926
MGI:2175099	F	MP:0013785	abnormal mammary gland bud morphology	Lef1<tm1Rug>/Lef1<tm1Rug>	involves: 129S2/SvPas * C57BL/6	N	7958926
MGI:2175121	F	MP:0004135	abnormal mammary gland embryonic development	Msx2<tm1Rilm>/Msx2<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6J)	N	10742104
MGI:2175122	M	MP:0006380	abnormal spermatid morphology	Map7<Gt(ROSABetageo)1Sor>/Map7<Gt(ROSABetageo)1Sor>	either: 129S4/SvJaeSor-Map7<Gt(ROSABetageo)1Sor> or (involves: 129S4/SvJaeSor * C57BL/6J)	N	10837026
MGI:2175122	M	MP:0001932	abnormal spermiogenesis	Map7<Gt(ROSABetageo)1Sor>/Map7<Gt(ROSABetageo)1Sor>	either: 129S4/SvJaeSor-Map7<Gt(ROSABetageo)1Sor> or (involves: 129S4/SvJaeSor * C57BL/6J)	N	10837026
MGI:2175122	M	MP:0001147	small testis	Map7<Gt(ROSABetageo)1Sor>/Map7<Gt(ROSABetageo)1Sor>	either: 129S4/SvJaeSor-Map7<Gt(ROSABetageo)1Sor> or (involves: 129S4/SvJaeSor * C57BL/6J)	N	10837026
MGI:2175122	M	MP:0004930	small epididymis	Map7<Gt(ROSABetageo)1Sor>/Map7<Gt(ROSABetageo)1Sor>	either: 129S4/SvJaeSor-Map7<Gt(ROSABetageo)1Sor> or (involves: 129S4/SvJaeSor * C57BL/6J)	N	10837026
MGI:2175122	M	MP:0001152	increased Leydig cell number	Map7<Gt(ROSABetageo)1Sor>/Map7<Gt(ROSABetageo)1Sor>	either: 129S4/SvJaeSor-Map7<Gt(ROSABetageo)1Sor> or (involves: 129S4/SvJaeSor * C57BL/6J)	N	10837026
MGI:2175122	M	MP:0001153	small seminiferous tubules	Map7<Gt(ROSABetageo)1Sor>/Map7<Gt(ROSABetageo)1Sor>	either: 129S4/SvJaeSor-Map7<Gt(ROSABetageo)1Sor> or (involves: 129S4/SvJaeSor * C57BL/6J)	N	10837026
MGI:2175122	M	MP:0002784	abnormal Sertoli cell morphology	Map7<Gt(ROSABetageo)1Sor>/Map7<Gt(ROSABetageo)1Sor>	either: 129S4/SvJaeSor-Map7<Gt(ROSABetageo)1Sor> or (involves: 129S4/SvJaeSor * C57BL/6J)	N	10837026
MGI:2175122	M	MP:0001925	male infertility	Map7<Gt(ROSABetageo)1Sor>/Map7<Gt(ROSABetageo)1Sor>	either: 129S4/SvJaeSor-Map7<Gt(ROSABetageo)1Sor> or (involves: 129S4/SvJaeSor * C57BL/6J)	N	10837026
MGI:2175139	F	MP:0000433	microcephaly	Nano/Nano<+>	involves: BALB/cAnNCrl * C3H/HeNCrl	N	10932191
MGI:2175150	M	MP:0000666	decreased prostate gland duct number	Nkx3-1<tm1Hha>/Nkx3-1<tm1Hha>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175150	M	MP:0013737	small bulbourethral gland	Nkx3-1<tm1Hha>/Nkx3-1<tm1Hha>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175150	M	MP:0001169	abnormal bulbourethral gland morphology	Nkx3-1<tm1Hha>/Nkx3-1<tm1Hha>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175150	M	MP:0031369	prostate gland dorsolateral lobe hyperplasia	Nkx3-1<tm1Hha>/Nkx3-1<tm1Hha>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175150	M	MP:0000664	small prostate gland anterior lobe	Nkx3-1<tm1Hha>/Nkx3-1<tm1Hha>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175150	M	MP:0000665	decreased ductal branching in the coagulating gland	Nkx3-1<tm1Hha>/Nkx3-1<tm1Hha>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175150	M	MP:0001380	reduced male mating frequency	Nkx3-1<tm1Hha>/Nkx3-1<tm1Hha>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175150	M	MP:0005305	prostate gland anterior lobe hyperplasia	Nkx3-1<tm1Hha>/Nkx3-1<tm1Hha>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175150	M	MP:0001158	abnormal prostate gland morphology	Nkx3-1<tm1Hha>/Nkx3-1<tm1Hha>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175150	M	MP:0009736	abnormal prostate gland branching morphogenesis	Nkx3-1<tm1Hha>/Nkx3-1<tm1Hha>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175150	M	MP:0001168	abnormal prostate gland epithelium morphology	Nkx3-1<tm1Hha>/Nkx3-1<tm1Hha>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175151	M	MP:0031369	prostate gland dorsolateral lobe hyperplasia	Nkx3-1<tm1Hha>/Nkx3-1<+>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175151	M	MP:0005305	prostate gland anterior lobe hyperplasia	Nkx3-1<tm1Hha>/Nkx3-1<+>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175151	M	MP:0001163	abnormal prostate gland anterior lobe morphology	Nkx3-1<tm1Hha>/Nkx3-1<+>	involves: 129S4/SvJae * C57BL/6	N	10906459
MGI:2175152	M	MP:0000666	decreased prostate gland duct number	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175152	M	MP:0031369	prostate gland dorsolateral lobe hyperplasia	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175152	M	MP:0000671	bulbourethral gland hypoplasia	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175152	M	MP:0009736	abnormal prostate gland branching morphogenesis	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175152	M	MP:0005305	prostate gland anterior lobe hyperplasia	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175152	M	MP:0001380	reduced male mating frequency	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175152	M	MP:0001163	abnormal prostate gland anterior lobe morphology	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175152	M	MP:0003607	abnormal prostate gland physiology	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175152	M	MP:0001168	abnormal prostate gland epithelium morphology	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175152	M	MP:0011781	abnormal bulbourethral gland physiology	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175152	M	MP:0013736	abnormal bulbourethral gland development	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175152	M	MP:0001167	prostate gland epithelial hyperplasia	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175153	M	MP:0001168	abnormal prostate gland epithelium morphology	Nkx3-1<tm1Mms>/Nkx3-1<+>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175153	M	MP:0003607	abnormal prostate gland physiology	Nkx3-1<tm1Mms>/Nkx3-1<+>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175153	M	MP:0005305	prostate gland anterior lobe hyperplasia	Nkx3-1<tm1Mms>/Nkx3-1<+>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175153	M	MP:0001167	prostate gland epithelial hyperplasia	Nkx3-1<tm1Mms>/Nkx3-1<+>	either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	N	10215624
MGI:2175195	M	MP:0001147	small testis	Otx1<tm1Asim>/Otx1<tm1Asim>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	9477321
MGI:2175195	F	MP:0001127	small ovary	Otx1<tm1Asim>/Otx1<tm1Asim>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	9477321
MGI:2175195	M	MP:0001155	arrest of spermatogenesis	Otx1<tm1Asim>/Otx1<tm1Asim>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	9477321
MGI:2175195	F	MP:0001130	abnormal ovarian folliculogenesis	Otx1<tm1Asim>/Otx1<tm1Asim>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	9477321
MGI:2175195	M	MP:0002216	abnormal seminiferous tubule morphology	Otx1<tm1Asim>/Otx1<tm1Asim>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	9477321
MGI:2175197	M	MP:0001146	abnormal testis morphology	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9808631
MGI:2175197	M	MP:0001154	seminiferous tubule degeneration	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9808631
MGI:2175197	M	MP:0001922	reduced male fertility	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9808631
MGI:2175197	F	MP:0001136	dilated uterine cervix	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9808631
MGI:2175197	F	MP:0001123	dilated uterus	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9808631
MGI:2175197	M	MP:0004901	decreased male germ cell number	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9808631
MGI:2175197	M	MP:0001156	abnormal spermatogenesis	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9808631
MGI:2175197	M	MP:0004852	decreased testis weight	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9808631
MGI:2175197	F	MP:0001144	vagina atresia	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9808631
MGI:2175197	F	MP:0001143	constricted vagina orifice	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9808631
MGI:2175197	M	MP:0001153	small seminiferous tubules	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9808631
MGI:2175197	F	MP:0001923	reduced female fertility	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9808631
MGI:2175197	M	MP:0001147	small testis	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9808631
MGI:2175206	F	MP:0001923	reduced female fertility	Pax6<Sey-H>/Pax6<+>	involves: 101/H * C3H/HeH	N	3794606
MGI:2175210	M	MP:0002687	oligozoospermia	Agtpbp1<pcd>/Agtpbp1<pcd>	involves: C57BR/cdJ * CBA	N	1061118
MGI:2175210	M	MP:0006362	abnormal male germ cell morphology	Agtpbp1<pcd>/Agtpbp1<pcd>	involves: C57BR/cdJ * CBA	N	1061118
MGI:2175210	M	MP:0001925	male infertility	Agtpbp1<pcd>/Agtpbp1<pcd>	involves: C57BR/cdJ * CBA	N	1061118
MGI:2175210	F	MP:0001923	reduced female fertility	Agtpbp1<pcd>/Agtpbp1<pcd>	involves: C57BR/cdJ * CBA	N	1061118
MGI:2175210	M	MP:0002675	asthenozoospermia	Agtpbp1<pcd>/Agtpbp1<pcd>	involves: C57BR/cdJ * CBA	N	1061118
MGI:2175211	M	MP:0001925	male infertility	Agtpbp1<pcd-3J>/Agtpbp1<pcd-3J>	involves: BALB/cByJ	N	11884758
MGI:2175211	M	MP:0002675	asthenozoospermia	Agtpbp1<pcd-3J>/Agtpbp1<pcd-3J>	involves: BALB/cByJ	N	11884758
MGI:2175211	M	MP:0006362	abnormal male germ cell morphology	Agtpbp1<pcd-3J>/Agtpbp1<pcd-3J>	involves: BALB/cByJ	N	11884758
MGI:2175211	M	MP:0002687	oligozoospermia	Agtpbp1<pcd-3J>/Agtpbp1<pcd-3J>	involves: BALB/cByJ	N	11884758
MGI:2175212	M	MP:0005159	azoospermia	Agtpbp1<pcd-Tg(Dhfr)1Jwg>/Agtpbp1<pcd-Tg(Dhfr)1Jwg>	involves: C57BL/6J * CD-1 * DBA/2J	N	2726749
MGI:2175212	M	MP:0001925	male infertility	Agtpbp1<pcd-Tg(Dhfr)1Jwg>/Agtpbp1<pcd-Tg(Dhfr)1Jwg>	involves: C57BL/6J * CD-1 * DBA/2J	N	2726749
MGI:2175212	M	MP:0001925	male infertility	Agtpbp1<pcd-Tg(Dhfr)1Jwg>/Agtpbp1<pcd-Tg(Dhfr)1Jwg>	involves: C57BL/6J * CD-1 * DBA/2J	N	MGI:63137
MGI:2175216	M	MP:0002826	tonic seizures	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	N	7700379
MGI:2175216	M	MP:0009302	increased renal fat pad weight	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	N	7700379
MGI:2175216	M	MP:0009288	increased epididymal fat pad weight	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	N	7700379
MGI:2175216	M	MP:0002083	premature death	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	N	7700379
MGI:2175216	M	MP:0003997	tonic-clonic seizures	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	N	7700379
MGI:2175216	M	MP:0001433	polyphagia	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	N	7700379
MGI:2175216	M	MP:0009747	impaired behavioral response to xenobiotic	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	N	7700379
MGI:2175216	M	MP:0002906	increased susceptibility to pharmacologically induced seizures	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	N	7700379
MGI:2175216	M	MP:0001441	increased grooming behavior	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	N	7700379
MGI:2175216	M	MP:0000008	increased white adipose tissue amount	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	N	7700379
MGI:2175216	M	MP:0005386	behavior/neurological phenotype	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	Y	7700379
MGI:2175216	M	MP:0003631	nervous system phenotype	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	Y	7700379
MGI:2175216	M	MP:0000951	sporadic seizures	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	N	7700379
MGI:2175216	M	MP:0001260	increased body weight	Htr2c<tm1Jul>/Y	either: (involves: 129S2/SvPas * C57BL/6J * DBA/2) or (involves: 129S4/SvJae * C57BL/6J * DBA/2)	N	7700379
MGI:2175217	F	MP:0005378	growth/size/body region phenotype	Irs4<tm1Lhd>/Irs4<tm1Lhd>	involves: 129S4/SvJae * C57BL/6	Y	10644546
MGI:2175217	F	MP:0001935	decreased litter size	Irs4<tm1Lhd>/Irs4<tm1Lhd>	involves: 129S4/SvJae * C57BL/6	N	10644546
MGI:2175217	F	MP:0005376	homeostasis/metabolism phenotype	Irs4<tm1Lhd>/Irs4<tm1Lhd>	involves: 129S4/SvJae * C57BL/6	Y	10644546
MGI:2175217	F	MP:0002161	abnormal fertility/fecundity	Irs4<tm1Lhd>/Irs4<tm1Lhd>	involves: 129S4/SvJae * C57BL/6	N	10644546
MGI:2175217	F	MP:0001386	abnormal maternal nurturing	Irs4<tm1Lhd>/Irs4<tm1Lhd>	involves: 129S4/SvJae * C57BL/6	N	10644546
MGI:2175217	F	MP:0005291	abnormal glucose tolerance	Irs4<tm1Lhd>/Irs4<tm1Lhd>	involves: 129S4/SvJae * C57BL/6	N	10644546
MGI:2175218	M	MP:0001262	decreased body weight	Irs4<tm1Lhd>/Y	involves: 129S4/SvJae * C57BL/6	N	10644546
MGI:2175218	M	MP:0001732	postnatal growth retardation	Irs4<tm1Lhd>/Y	involves: 129S4/SvJae * C57BL/6	N	10644546
MGI:2175218	M	MP:0001935	decreased litter size	Irs4<tm1Lhd>/Y	involves: 129S4/SvJae * C57BL/6	N	10644546
MGI:2175218	M	MP:0005560	decreased circulating glucose level	Irs4<tm1Lhd>/Y	involves: 129S4/SvJae * C57BL/6	N	10644546
MGI:2175218	M	MP:0005293	impaired glucose tolerance	Irs4<tm1Lhd>/Y	involves: 129S4/SvJae * C57BL/6	N	10644546
MGI:2175218	M	MP:0002161	abnormal fertility/fecundity	Irs4<tm1Lhd>/Y	involves: 129S4/SvJae * C57BL/6	N	10644546
MGI:2175223	M	MP:0011765	oroticaciduria	Otc<spf-ash>/Y	Not Specified	N	3162766
MGI:2175223	M	MP:0008469	abnormal protein level	Otc<spf-ash>/Y	Not Specified	N	2920015
MGI:2175223	M	MP:0005584	abnormal enzyme/coenzyme activity	Otc<spf-ash>/Y	Not Specified	N	2920015
MGI:2175223	M	MP:0000599	enlarged liver	Otc<spf-ash>/Y	Not Specified	N	2920015
MGI:2175223	M	MP:0002981	increased liver weight	Otc<spf-ash>/Y	Not Specified	N	2920015
MGI:2175223	M	MP:0011588	decreased ornithine carbamoyltransferase activity	Otc<spf-ash>/Y	Not Specified	N	6623083
MGI:2175223	M	MP:0000416	sparse hair	Otc<spf-ash>/Y	Not Specified	N	3162766
MGI:2175223	M	MP:0005309	increased circulating ammonia level	Otc<spf-ash>/Y	Not Specified	N	3162766
MGI:2175223	M	MP:0006036	abnormal mitochondrial physiology	Otc<spf-ash>/Y	Not Specified	N	2920015
MGI:2175223	M	MP:0001211	wrinkled skin	Otc<spf-ash>/Y	Not Specified	N	3162766
MGI:2175224	F	MP:0000416	sparse hair	Otc<spf-ash>/Otc<+>	Not Specified	N	4603259
MGI:2175225	F	MP:0005266	abnormal metabolism	Otc<spf>/Otc<spf>	involves: CD-1	N	1575747
MGI:2175225	F	MP:0005309	increased circulating ammonia level	Otc<spf>/Otc<spf>	involves: CD-1	N	1575747
MGI:2175225	F	MP:0005332	abnormal amino acid level	Otc<spf>/Otc<spf>	involves: CD-1	N	1575747
MGI:2175226	F	MP:0000422	delayed hair appearance	Otc<spf>/Otc<+>	Not Specified	N	MGI:74395
MGI:2175226	F	MP:0000418	focal hair loss	Otc<spf>/Otc<+>	Not Specified	N	MGI:74395
MGI:2175226	F	MP:0011765	oroticaciduria	Otc<spf>/Otc<+>	Not Specified	N	7707692
MGI:2175226	F	MP:0005311	abnormal circulating amino acid level	Otc<spf>/Otc<+>	Not Specified	N	7707692
MGI:2175226	F	MP:0011588	decreased ornithine carbamoyltransferase activity	Otc<spf>/Otc<+>	Not Specified	N	3981356
MGI:2175226	F	MP:0005584	abnormal enzyme/coenzyme activity	Otc<spf>/Otc<+>	Not Specified	N	7707692
MGI:2175363	F	MP:0002418	increased susceptibility to viral infection	Nsv1<C57BL/6J>/?	involves: BALB/cBy * C57BL/6J	N	11507212
MGI:2175496	F	MP:0004904	increased uterus weight	Estq2<C57BL/6J>/?,Estq3<C57BL/6J>/?	involves: C3H/HeJ * C57BL/6J	N	9927277
MGI:2175541	F	MP:0002016	ovary cyst	Ots1<LT/Sv>/Ots1<LT/Sv>	involves: C57BL/6J * LT/Sv	N	9044831
MGI:2175542	F	MP:0002016	ovary cyst	Ots1<LT/Sv>/Ots1<C57BL/6J>	involves: C57BL/6J * LT/Sv	N	9044831
MGI:2175671	F	MP:0001120	abnormal uterus morphology	Estq1<C57BL/6J>/?,Estq4<C57BL/6J>/?	involves: C3H/HeJ * C57BL/6J	N	9927277
MGI:2175698	M	MP:0006378	abnormal spermatogonia morphology	Apaf1<tm1Her>/Apaf1<tm1Her>	involves: 129S6/SvEvTac * C57BL/6J	N	10656767
MGI:2175698	M	MP:0005159	azoospermia	Apaf1<tm1Her>/Apaf1<tm1Her>	involves: 129S6/SvEvTac * C57BL/6J	N	10656767
MGI:2175698	M	MP:0002216	abnormal seminiferous tubule morphology	Apaf1<tm1Her>/Apaf1<tm1Her>	involves: 129S6/SvEvTac * C57BL/6J	N	10656767
MGI:2175698	F	MP:0001923	reduced female fertility	Apaf1<tm1Her>/Apaf1<tm1Her>	involves: 129S6/SvEvTac * C57BL/6J	N	10656767
MGI:2175698	M	MP:0001925	male infertility	Apaf1<tm1Her>/Apaf1<tm1Her>	involves: 129S6/SvEvTac * C57BL/6J	N	10656767
MGI:2175703	F	MP:0004805	absent oocytes	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175703	F	MP:0001926	female infertility	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175703	F	MP:0001127	small ovary	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175703	M	MP:0002216	abnormal seminiferous tubule morphology	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175703	M	MP:0005159	azoospermia	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175703	M	MP:0001925	male infertility	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175703	F	MP:0009009	absent estrous cycle	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175703	M	MP:0001147	small testis	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175703	F	MP:0001120	abnormal uterus morphology	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175703	M	MP:0001145	abnormal male reproductive system morphology	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175703	M	MP:0001155	arrest of spermatogenesis	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175703	F	MP:0009021	absent estrus	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175703	F	MP:0002777	absent ovarian follicles	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175703	F	MP:0001119	abnormal female reproductive system morphology	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	8689683
MGI:2175706	F	MP:0004805	absent oocytes	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	N	8843194
MGI:2175706	F	MP:0002777	absent ovarian follicles	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	N	8843194
MGI:2175706	M	MP:0008261	arrest of male meiosis	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	N	8843194
MGI:2175706	M	MP:0001925	male infertility	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	N	8843194
MGI:2175706	F	MP:0013236	ovary degeneration	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	N	8843194
MGI:2175706	F	MP:0001926	female infertility	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	N	8843194
MGI:2175706	F	MP:0005168	abnormal female meiosis	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	N	8843194
MGI:2175707	M	MP:0001925	male infertility	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	N	10716718
MGI:2175707	F	MP:0001926	female infertility	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	N	10716718
MGI:2175708	M	MP:0001146	abnormal testis morphology	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	N	8917548
MGI:2175708	M	MP:0001147	small testis	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	N	8917548
MGI:2175708	M	MP:0001925	male infertility	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	N	8917548
MGI:2175708	M	MP:0005159	azoospermia	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	N	8917548
MGI:2175711	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Atp7a<Mo>/Y	Not Specified	N	13103353
MGI:2175711	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Atp7a<Mo>/Y	Not Specified	N	MGI:61250
MGI:2175712	F	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo>/Atp7a<+>	Not Specified	N	13103353
MGI:2175712	F	MP:0001274	curly vibrissae	Atp7a<Mo>/Atp7a<+>	Not Specified	N	13103353
MGI:2175712	F	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo>/Atp7a<+>	Not Specified	N	MGI:61250
MGI:2175712	F	MP:0011101	prenatal lethality, incomplete penetrance	Atp7a<Mo>/Atp7a<+>	Not Specified	N	MGI:61250
MGI:2175712	F	MP:0011086	postnatal lethality, incomplete penetrance	Atp7a<Mo>/Atp7a<+>	Not Specified	N	MGI:61250
MGI:2175712	F	MP:0001935	decreased litter size	Atp7a<Mo>/Atp7a<+>	Not Specified	N	MGI:61250
MGI:2175713	M	MP:0001262	decreased body weight	Avpr2<tm1Jwe>/Y	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11104789
MGI:2175713	M	MP:0003019	increased circulating chloride level	Avpr2<tm1Jwe>/Y	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11104789
MGI:2175713	M	MP:0011085	postnatal lethality, complete penetrance	Avpr2<tm1Jwe>/Y	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11104789
MGI:2175713	M	MP:0000519	hydronephrosis	Avpr2<tm1Jwe>/Y	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11104789
MGI:2175713	M	MP:0005633	increased circulating sodium level	Avpr2<tm1Jwe>/Y	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11104789
MGI:2175713	M	MP:0000189	hypoglycemia	Avpr2<tm1Jwe>/Y	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11104789
MGI:2175713	M	MP:0003853	dry skin	Avpr2<tm1Jwe>/Y	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11104789
MGI:2175713	M	MP:0002988	decreased urine osmolality	Avpr2<tm1Jwe>/Y	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11104789
MGI:2175713	M	MP:0002608	increased hematocrit	Avpr2<tm1Jwe>/Y	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11104789
MGI:2175725	M	MP:0001922	reduced male fertility	Bdnf<tm2(Ntf5)Jae>/Bdnf<tm2(Ntf5)Jae>	involves: 129S4/SvJae	N	10725924
MGI:2175725	F	MP:0001926	female infertility	Bdnf<tm2(Ntf5)Jae>/Bdnf<tm2(Ntf5)Jae>	involves: 129S4/SvJae	N	10725924
MGI:2175758	M	MP:0031366	decreased prostate gland dorsolateral lobe weight	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas	N	16014817
MGI:2175758	M	MP:0009381	abnormal prostate gland dorsolateral lobe morphology	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas	N	16014817
MGI:2175758	M	MP:0004910	decreased seminal vesicle weight	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas	N	16014817
MGI:2175759	F	MP:0001926	female infertility	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	N	8646780
MGI:2175759	F	MP:0009006	prolonged estrous cycle	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	N	8646780
MGI:2175759	F	MP:0002679	abnormal corpus luteum morphology	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	N	8646780
MGI:2175759	F	MP:0009017	prolonged estrus	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	N	8646780
MGI:2175760	M	MP:0001149	testicular hyperplasia	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	N	8646779
MGI:2175760	F	MP:0008868	abnormal granulosa cell morphology	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	N	8646779
MGI:2175760	F	MP:0001926	female infertility	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	N	8646779
MGI:2175760	F	MP:0001120	abnormal uterus morphology	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	N	8646779
MGI:2175760	F	MP:0001129	impaired ovarian folliculogenesis	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	N	8646779
MGI:2175760	F	MP:0001134	absent corpus luteum	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	N	8646779
MGI:2175760	M	MP:0001148	enlarged testis	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	N	8646779
MGI:2175760	F	MP:0011130	absent tertiary ovarian follicles	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	N	8646779
MGI:2175760	F	MP:0009092	endometrium hyperplasia	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	N	8646779
MGI:2175760	F	MP:0001131	abnormal ovarian follicle morphology	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	N	8646779
MGI:2175760	F	MP:0004832	enlarged ovary	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	N	8646779
MGI:2175760	M	MP:0004958	enlarged prostate gland	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	N	8646779
MGI:2175761	F	MP:0001926	female infertility	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	N	8646781
MGI:2175761	F	MP:0001134	absent corpus luteum	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	N	8646781
MGI:2175766	M	MP:0001145	abnormal male reproductive system morphology	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	N	10731669
MGI:2175766	M	MP:0009735	abnormal prostate gland development	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	N	10731669
MGI:2175766	F	MP:0001119	abnormal female reproductive system morphology	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	N	10731669
MGI:2175766	M	MP:0001938	delayed sexual maturation	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	N	10731669
MGI:2175766	F	MP:0001926	female infertility	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	N	10731669
MGI:2175766	F	MP:0003572	abnormal uterus development	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	N	10731669
MGI:2175766	F	MP:0031239	increased atretic ovarian follicle number	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	N	10731669
MGI:2175766	F	MP:0001144	vagina atresia	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	N	10731669
MGI:2175766	F	MP:0009709	hydrometra	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	N	10731669
MGI:2175766	M	MP:0003830	abnormal testis development	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	N	10731669
MGI:2175766	M	MP:0013317	abnormal seminal vesicle development	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	N	10731669
MGI:2175770	M	MP:0006379	abnormal spermatocyte morphology	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	N	28652370
MGI:2175770	M	MP:0002687	oligozoospermia	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	N	28652370
MGI:2175770	M	MP:0004852	decreased testis weight	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	N	28652370
MGI:2175773	M	MP:0001152	increased Leydig cell number	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	N	11287627
MGI:2175773	M	MP:0006262	increased testis tumor incidence	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	N	10880462
MGI:2175773	F	MP:0000630	mammary gland hyperplasia	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	N	10880462
MGI:2175773	F	MP:0009504	abnormal mammary gland epithelium morphology	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	N	10880462
MGI:2175773	M	MP:0013602	abnormal Leydig cell differentiation	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	N	11287627
MGI:2175773	M	MP:0001148	enlarged testis	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	N	11287627
MGI:2175774	M	MP:0001147	small testis	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	N	9744866
MGI:2175776	M	MP:0003205	testicular atrophy	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * C57BL/6	N	10594039
MGI:2175776	M	MP:0020550	multinucleated giant male germ cells	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * C57BL/6	N	10594039
MGI:2175776	M	MP:0001156	abnormal spermatogenesis	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * C57BL/6	N	10594039
MGI:2175776	M	MP:0014052	increased male germ cell apoptosis	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * C57BL/6	N	10594039
MGI:2175777	F	MP:0001728	failure of embryo implantation	Cdx2<tm1Fbe>/Cdx2<tm1Fbe>	involves: 129S1/Sv * C57BL/6J	N	9052785
MGI:2175839	F	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta-40H>/Eda<+>	involves: BALB/c * C3H/HeN	N	10932191
MGI:2175851	M	MP:0001925	male infertility	En1<tm4(en)Alj>/En1<tm4(en)Alj>	involves: 129S1/Sv * 129X1/SvJ	N	9778510
MGI:2175868	F	MP:0001382	abnormal nursing	Espn<je>/Espn<je>	involves: fancier's dancing mouse	N	16588504
MGI:2175870	F	MP:0001926	female infertility	Eya1<bor>/Eya1<bor>	C3HeB/FeJ-Eya1<bor>	N	10072433
MGI:2175872	F	MP:0002551	abnormal blood coagulation	F9<tm1Emg>/F9<+>	involves: 129S/SvEv * C57BL/6J	N	9639513
MGI:2175873	F	MP:0005606	increased bleeding time	F9<tm1Ver>/F9<tm1Ver>	involves: 129/Sv * C57BL/6	N	9326649
MGI:2175873	F	MP:0005023	abnormal wound healing	F9<tm1Ver>/F9<tm1Ver>	involves: 129/Sv * C57BL/6	N	9326649
MGI:2175873	F	MP:0002551	abnormal blood coagulation	F9<tm1Ver>/F9<tm1Ver>	involves: 129/Sv * C57BL/6	N	9326649
MGI:2175873	F	MP:0005376	homeostasis/metabolism phenotype	F9<tm1Ver>/F9<tm1Ver>	involves: 129/Sv * C57BL/6	Y	9326649
MGI:2175884	F	MP:0013721	abnormal mammary placode morphology	Fgf10<tm1Ska>/Fgf10<tm1Ska>	involves: C57BL/6 * CBA	N	16720875
MGI:2175884	F	MP:0013721	abnormal mammary placode morphology	Fgf10<tm1Ska>/Fgf10<tm1Ska>	involves: C57BL/6 * CBA	N	11782400
MGI:2175884	F	MP:0000662	abnormal branching of the mammary ductal tree	Fgf10<tm1Ska>/Fgf10<tm1Ska>	involves: C57BL/6 * CBA	N	11782400
MGI:2175910	M	MP:0006401	absent male preputial gland	Apc<tm1Rfo>/Apc<tm1Rfo>	involves: 129P2/OlaHsd * C57BL/6J	N	10346819
MGI:2176333	F	MP:0004856	decreased ovary weight	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	N	9660953
MGI:2176333	M	MP:0004852	decreased testis weight	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	N	9660953
MGI:2176333	F	MP:0001926	female infertility	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	N	9660953
MGI:2176333	F	MP:0004805	absent oocytes	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	N	22549958
MGI:2176333	F	MP:0004805	absent oocytes	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	N	9660953
MGI:2176333	F	MP:0005168	abnormal female meiosis	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	N	9660953
MGI:2176333	M	MP:0001156	abnormal spermatogenesis	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	N	9660953
MGI:2176333	M	MP:0008261	arrest of male meiosis	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	N	9660953
MGI:2176333	M	MP:0005159	azoospermia	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	N	9660953
MGI:2176333	F	MP:0001931	abnormal oogenesis	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	N	9660953
MGI:2176333	M	MP:0001925	male infertility	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	N	9660953
MGI:2176333	F	MP:0002777	absent ovarian follicles	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	N	9660953
MGI:2176343	M	MP:0004543	abnormal sperm physiology	Pltp<tm1Jia>/Pltp<tm1Jia>	involves: C57BL/6	N	16467369
MGI:2176343	M	MP:0001922	reduced male fertility	Pltp<tm1Jia>/Pltp<tm1Jia>	involves: C57BL/6	N	16467369
MGI:2176343	M	MP:0002675	asthenozoospermia	Pltp<tm1Jia>/Pltp<tm1Jia>	involves: C57BL/6	N	16467369
MGI:2176343	M	MP:0002660	abnormal caput epididymis morphology	Pltp<tm1Jia>/Pltp<tm1Jia>	involves: C57BL/6	N	16467369
MGI:2176343	M	MP:0002662	abnormal cauda epididymis morphology	Pltp<tm1Jia>/Pltp<tm1Jia>	involves: C57BL/6	N	16467369
MGI:2176447	F	MP:0001265	decreased body size	Esx1<tm1Bhr>/Esx1<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176447	F	MP:0012108	increased trophoblast glycogen cell number	Esx1<tm1Bhr>/Esx1<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176447	F	MP:0001712	abnormal placenta development	Esx1<tm1Bhr>/Esx1<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176447	F	MP:0011531	abnormal syncytiotrophoblast morphology	Esx1<tm1Bhr>/Esx1<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176447	F	MP:0004920	increased placenta weight	Esx1<tm1Bhr>/Esx1<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176447	F	MP:0004255	abnormal spongiotrophoblast layer morphology	Esx1<tm1Bhr>/Esx1<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176447	F	MP:0004201	fetal growth retardation	Esx1<tm1Bhr>/Esx1<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176447	F	MP:0003231	abnormal placenta vasculature	Esx1<tm1Bhr>/Esx1<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176447	F	MP:0005031	abnormal trophoblast layer morphology	Esx1<tm1Bhr>/Esx1<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176448	M	MP:0001265	decreased body size	Esx1<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176448	M	MP:0001712	abnormal placenta development	Esx1<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176448	M	MP:0004201	fetal growth retardation	Esx1<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176448	M	MP:0003231	abnormal placenta vasculature	Esx1<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176448	M	MP:0004920	increased placenta weight	Esx1<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176448	M	MP:0011531	abnormal syncytiotrophoblast morphology	Esx1<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176448	M	MP:0005031	abnormal trophoblast layer morphology	Esx1<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176448	M	MP:0012108	increased trophoblast glycogen cell number	Esx1<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176448	M	MP:0004255	abnormal spongiotrophoblast layer morphology	Esx1<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:2176479	F	MP:0003845	abnormal decidualization	Fgfr2<tm1Lni>/Fgfr2<tm1Lni>	involves: 129S1/Sv * 129X1/SvJ * MF1	N	9560232
MGI:2176491	F	MP:0009009	absent estrous cycle	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	F	MP:0001926	female infertility	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	M	MP:0002687	oligozoospermia	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	M	MP:0001925	male infertility	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	F	MP:0001134	absent corpus luteum	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	M	MP:0020869	immotile sperm	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	M	MP:0004852	decreased testis weight	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	F	MP:0031422	failure of superovulation	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	M	MP:0001153	small seminiferous tubules	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	M	MP:0001147	small testis	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	F	MP:0005158	ovary hypoplasia	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	F	MP:0009093	oocyte degeneration	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	F	MP:0011130	absent tertiary ovarian follicles	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	M	MP:0005148	seminal vesicle hypoplasia	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	M	MP:0004701	decreased circulating insulin-like growth factor I level	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	F	MP:0001129	impaired ovarian folliculogenesis	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	M	MP:0002780	decreased circulating testosterone level	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	M	MP:0030983	failure of copulatory plug deposition	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	M	MP:0004932	epididymis hypoplasia	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	F	MP:0001121	uterus hypoplasia	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	M	MP:0005123	increased circulating growth hormone level	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	F	MP:0005181	decreased circulating estradiol level	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176491	M	MP:0002790	decreased circulating follicle stimulating hormone level	Ggt1<tm1Zuk>/Ggt1<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11089562
MGI:2176533	F	MP:0000662	abnormal branching of the mammary ductal tree	Areg<tm1Dle>/Areg<tm1Dle>	involves: 129P2/OlaHsd * C57BL/6	N	10331984
MGI:2176533	F	MP:0006269	abnormal mammary gland growth during pregnancy	Areg<tm1Dle>/Areg<tm1Dle>	involves: 129P2/OlaHsd * C57BL/6	N	10331984
MGI:2176533	F	MP:0013716	hypolactation	Areg<tm1Dle>/Areg<tm1Dle>	involves: 129P2/OlaHsd * C57BL/6	N	10331984
MGI:2176534	F	MP:0013716	hypolactation	Areg<tm1Dle>/Areg<tm1Dle>,Egf<tm1Dle>/Egf<tm1Dle>,Tgfa<tm1Unc>/Tgfa<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6	N	10331984
MGI:2176534	F	MP:0006269	abnormal mammary gland growth during pregnancy	Areg<tm1Dle>/Areg<tm1Dle>,Egf<tm1Dle>/Egf<tm1Dle>,Tgfa<tm1Unc>/Tgfa<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6	N	10331984
MGI:2176534	F	MP:0000662	abnormal branching of the mammary ductal tree	Areg<tm1Dle>/Areg<tm1Dle>,Egf<tm1Dle>/Egf<tm1Dle>,Tgfa<tm1Unc>/Tgfa<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6	N	10331984
MGI:2176536	F	MP:0001882	abnormal lactation	Egfr<wa2>/Egfr<wa2>	B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt>/J	N	7533293
MGI:2176536	F	MP:0000627	abnormal mammary gland morphology	Egfr<wa2>/Egfr<wa2>	B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt>/J	N	7533293
MGI:2176542	F	MP:0001923	reduced female fertility	Nr2e1<frc>/Nr2e1<frc>	either: B6.129-Nr2e1<frc> or 129P3/JEms.Cg-Nr2e1<frc> or B6129F1-Nr2e1<frc>	N	11997145
MGI:2176542	F	MP:0001382	abnormal nursing	Nr2e1<frc>/Nr2e1<frc>	either: B6.129-Nr2e1<frc> or 129P3/JEms.Cg-Nr2e1<frc> or B6129F1-Nr2e1<frc>	N	11997145
MGI:2176701	M	MP:0001147	small testis	Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>	involves: 129S6/SvEvTac * C57BL/6	N	10894153
MGI:2176701	F	MP:0001923	reduced female fertility	Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>	involves: 129S6/SvEvTac * C57BL/6	N	10894153
MGI:2176701	M	MP:0001925	male infertility	Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>	involves: 129S6/SvEvTac * C57BL/6	N	10894153
MGI:2176701	F	MP:0011121	decreased primordial ovarian follicle number	Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>	involves: 129S6/SvEvTac * C57BL/6	N	10894153
MGI:2176704	F	MP:0001130	abnormal ovarian folliculogenesis	Bax<tm1Sjk>/Bax<+>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	10894153
MGI:2176704	M	MP:0001925	male infertility	Bax<tm1Sjk>/Bax<+>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	10894153
MGI:2176704	M	MP:0004901	decreased male germ cell number	Bax<tm1Sjk>/Bax<+>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	10894153
MGI:2176707	M	MP:0000530	abnormal kidney vasculature morphology	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0005326	abnormal podocyte morphology	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0003606	kidney failure	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0002705	dilated renal tubule	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0011483	renal glomerular synechia	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0011453	abnormal glomerular capillary endothelium morphology	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0011430	mesangiolysis	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0011290	decreased nephron number	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0011294	renal glomerulus hypertrophy	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0011353	expanded mesangial matrix	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0009641	kidney degeneration	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0005264	glomerulosclerosis	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0004505	decreased renal glomerulus number	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0011408	renal tubule hypertrophy	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0000521	abnormal kidney cortex morphology	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0011368	increased kidney apoptosis	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0011498	abnormal glomerular capsule parietal layer morphology	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0002989	small kidney	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0008140	podocyte foot process effacement	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0011500	decreased glomerular capsule space	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0003918	decreased kidney weight	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176707	M	MP:0011369	increased renal glomerulus apoptosis	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	N	9794553
MGI:2176718	F	MP:0009361	abnormal primordial ovarian follicle morphology	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	N	7628407
MGI:2176718	F	MP:0004805	absent oocytes	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	N	7628407
MGI:2176736	M	MP:0001147	small testis	Bcl2l2<Gt(ROSA)41Sor>/Bcl2l2<Gt(ROSA)41Sor>	involves: 129S5/SvEvBrd	N	9500547
MGI:2176736	M	MP:0004901	decreased male germ cell number	Bcl2l2<Gt(ROSA)41Sor>/Bcl2l2<Gt(ROSA)41Sor>	involves: 129S5/SvEvBrd	N	9500547
MGI:2176736	M	MP:0004910	decreased seminal vesicle weight	Bcl2l2<Gt(ROSA)41Sor>/Bcl2l2<Gt(ROSA)41Sor>	involves: 129S5/SvEvBrd	N	9500547
MGI:2176736	M	MP:0002216	abnormal seminiferous tubule morphology	Bcl2l2<Gt(ROSA)41Sor>/Bcl2l2<Gt(ROSA)41Sor>	involves: 129S5/SvEvBrd	N	9500547
MGI:2176736	M	MP:0001925	male infertility	Bcl2l2<Gt(ROSA)41Sor>/Bcl2l2<Gt(ROSA)41Sor>	involves: 129S5/SvEvBrd	N	9500547
MGI:2176737	M	MP:0005159	azoospermia	Bcl2l2<tm1Sco>/Bcl2l2<tm1Sco>	involves: 129S1/Sv * C57BL/6 * FVB/N	N	9770502
MGI:2176737	M	MP:0005250	decreased Sertoli cell number	Bcl2l2<tm1Sco>/Bcl2l2<tm1Sco>	involves: 129S1/Sv * C57BL/6 * FVB/N	N	9770502
MGI:2176737	M	MP:0001925	male infertility	Bcl2l2<tm1Sco>/Bcl2l2<tm1Sco>	involves: 129S1/Sv * C57BL/6 * FVB/N	N	9770502
MGI:2176737	M	MP:0002160	abnormal reproductive system morphology	Bcl2l2<tm1Sco>/Bcl2l2<tm1Sco>	involves: 129S1/Sv * C57BL/6 * FVB/N	N	9770502
MGI:2176737	M	MP:0001153	small seminiferous tubules	Bcl2l2<tm1Sco>/Bcl2l2<tm1Sco>	involves: 129S1/Sv * C57BL/6 * FVB/N	N	9770502
MGI:2176737	M	MP:0020550	multinucleated giant male germ cells	Bcl2l2<tm1Sco>/Bcl2l2<tm1Sco>	involves: 129S1/Sv * C57BL/6 * FVB/N	N	9770502
MGI:2176737	M	MP:0014052	increased male germ cell apoptosis	Bcl2l2<tm1Sco>/Bcl2l2<tm1Sco>	involves: 129S1/Sv * C57BL/6 * FVB/N	N	9770502
MGI:2176737	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Bcl2l2<tm1Sco>/Bcl2l2<tm1Sco>	involves: 129S1/Sv * C57BL/6 * FVB/N	N	9770502
MGI:2176756	F	MP:0001923	reduced female fertility	Bdnf<tm3Jae>/Bdnf<tm3Jae>,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * CBA/J	N	11579207
MGI:2176784	F	MP:0000662	abnormal branching of the mammary ductal tree	Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(Wap-cre)11738Mam/0	involves: 129S6/SvEvTac * Black Swiss	N	10319859
MGI:2176784	F	MP:0006271	abnormal involution of the mammary gland	Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(Wap-cre)11738Mam/0	involves: 129S6/SvEvTac * Black Swiss	N	10319859
MGI:2176784	F	MP:0000628	abnormal mammary gland development	Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(Wap-cre)11738Mam/0	involves: 129S6/SvEvTac * Black Swiss	N	10319859
MGI:2176784	F	MP:0006269	abnormal mammary gland growth during pregnancy	Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(Wap-cre)11738Mam/0	involves: 129S6/SvEvTac * Black Swiss	N	10319859
MGI:2176785	F	MP:0000662	abnormal branching of the mammary ductal tree	Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0	involves: 129S6/SvEvTac * Black Swiss * FVB	N	10319859
MGI:2176785	F	MP:0006271	abnormal involution of the mammary gland	Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0	involves: 129S6/SvEvTac * Black Swiss * FVB	N	10319859
MGI:2176785	F	MP:0000628	abnormal mammary gland development	Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0	involves: 129S6/SvEvTac * Black Swiss * FVB	N	10319859
MGI:2176785	F	MP:0006269	abnormal mammary gland growth during pregnancy	Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0	involves: 129S6/SvEvTac * Black Swiss * FVB	N	10319859
MGI:2176819	M	MP:0005449	abnormal food intake	Grpr<tm1Jfb>/Y	involves: 129X1/SvJ * C57BL/6J	N	9501238
MGI:2176820	F	MP:0002169	no abnormal phenotype detected	Grpr<tm1Jfb>/Grpr<tm1Jfb>	involves: 129X1/SvJ * C57BL/6J	N	9501238
MGI:2176876	F	MP:0001053	abnormal neuromuscular synapse morphology	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0000747	muscle weakness	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0000160	kyphosis	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0000160	kyphosis	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176876	F	MP:0002106	abnormal muscle physiology	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0001265	decreased body size	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0000752	dystrophic muscle	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176876	F	MP:0000752	dystrophic muscle	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0004036	abnormal muscle relaxation	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0002109	abnormal limb morphology	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176876	F	MP:0002109	abnormal limb morphology	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0000749	muscle degeneration	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0002083	premature death	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176876	F	MP:0002083	premature death	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0006085	myocardium necrosis	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0003852	skeletal muscle necrosis	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0003851	skeletal muscle interstitial fibrosis	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0001406	abnormal gait	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0005330	cardiomyopathy	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0005330	cardiomyopathy	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176876	F	MP:0001732	postnatal growth retardation	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176876	F	MP:0001732	postnatal growth retardation	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	9288752
MGI:2176876	F	MP:0001053	abnormal neuromuscular synapse morphology	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10719885
MGI:2176879	F	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0002083	premature death	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0000752	dystrophic muscle	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0009398	abnormal skeletal muscle fiber size	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0001263	weight loss	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0000160	kyphosis	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0003852	skeletal muscle necrosis	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0003851	skeletal muscle interstitial fibrosis	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0000748	progressive muscle weakness	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0000556	abnormal hindlimb morphology	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0001951	abnormal breathing pattern	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0001053	abnormal neuromuscular synapse morphology	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0001406	abnormal gait	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0001504	abnormal posture	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176879	F	MP:0001402	decreased locomotor activity	Dmd<mdx>/Dmd<mdx>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	N	9288751
MGI:2176880	M	MP:0002127	abnormal cardiovascular system morphology	Dmd<Gt(ROSABetageo)1Mpd>/Y	involves: 129S1/Sv	N	9626497
MGI:2176880	M	MP:0002106	abnormal muscle physiology	Dmd<Gt(ROSABetageo)1Mpd>/Y	involves: 129S1/Sv	N	9626497
MGI:2176880	M	MP:0002108	abnormal muscle morphology	Dmd<Gt(ROSABetageo)1Mpd>/Y	involves: 129S1/Sv	N	9626497
MGI:2176880	M	MP:0000462	abnormal digestive system morphology	Dmd<Gt(ROSABetageo)1Mpd>/Y	involves: 129S1/Sv	N	9626497
MGI:2176881	F	MP:0002127	abnormal cardiovascular system morphology	Dmd<Gt(ROSABetageo)1Mpd>/Dmd<Gt(ROSABetageo)1Mpd>	involves: 129S1/Sv	N	9626497
MGI:2176881	F	MP:0002108	abnormal muscle morphology	Dmd<Gt(ROSABetageo)1Mpd>/Dmd<Gt(ROSABetageo)1Mpd>	involves: 129S1/Sv	N	9626497
MGI:2176881	F	MP:0002106	abnormal muscle physiology	Dmd<Gt(ROSABetageo)1Mpd>/Dmd<Gt(ROSABetageo)1Mpd>	involves: 129S1/Sv	N	9626497
MGI:2176891	M	MP:0002083	premature death	Dmd<mdx>/Y,Dtna<tm1Jrs>/Dtna<tm1Jrs>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176891	M	MP:0000752	dystrophic muscle	Dmd<mdx>/Y,Dtna<tm1Jrs>/Dtna<tm1Jrs>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176891	M	MP:0001053	abnormal neuromuscular synapse morphology	Dmd<mdx>/Y,Dtna<tm1Jrs>/Dtna<tm1Jrs>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10719885
MGI:2176891	M	MP:0002109	abnormal limb morphology	Dmd<mdx>/Y,Dtna<tm1Jrs>/Dtna<tm1Jrs>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176891	M	MP:0005330	cardiomyopathy	Dmd<mdx>/Y,Dtna<tm1Jrs>/Dtna<tm1Jrs>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176891	M	MP:0011086	postnatal lethality, incomplete penetrance	Dmd<mdx>/Y,Dtna<tm1Jrs>/Dtna<tm1Jrs>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176891	M	MP:0003852	skeletal muscle necrosis	Dmd<mdx>/Y,Dtna<tm1Jrs>/Dtna<tm1Jrs>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176891	M	MP:0001732	postnatal growth retardation	Dmd<mdx>/Y,Dtna<tm1Jrs>/Dtna<tm1Jrs>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176891	M	MP:0000160	kyphosis	Dmd<mdx>/Y,Dtna<tm1Jrs>/Dtna<tm1Jrs>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176892	M	MP:0001053	abnormal neuromuscular synapse morphology	Dmd<mdx>/Y,Dtna<tm1Jrs>/Dtna<tm1Jrs>	involves: 129X1/SvJ * C57BL/10ScSn	N	10719885
MGI:2176892	M	MP:0005330	cardiomyopathy	Dmd<mdx>/Y,Dtna<tm1Jrs>/Dtna<tm1Jrs>	involves: 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176892	M	MP:0000752	dystrophic muscle	Dmd<mdx>/Y,Dtna<tm1Jrs>/Dtna<tm1Jrs>	involves: 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176892	M	MP:0002083	premature death	Dmd<mdx>/Y,Dtna<tm1Jrs>/Dtna<tm1Jrs>	involves: 129X1/SvJ * C57BL/10ScSn	N	10559919
MGI:2176912	F	MP:0003631	nervous system phenotype	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae * C57BL/6	Y	8790370
MGI:2176912	F	MP:0000598	abnormal liver morphology	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae * C57BL/6	N	8790370
MGI:2176912	F	MP:0003871	abnormal myelin sheath morphology	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:2176912	F	MP:0000921	demyelination	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:2176912	F	MP:0005386	behavior/neurological phenotype	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae * C57BL/6	Y	9700485
MGI:2176912	F	MP:0001262	decreased body weight	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae * C57BL/6	N	8790370
MGI:2176912	F	MP:0003632	abnormal nervous system morphology	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:2176912	F	MP:0001106	abnormal Schwann cell morphology	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:2176912	F	MP:0005404	abnormal axon morphology	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:2176915	M	MP:0000921	demyelination	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:2176915	M	MP:0001106	abnormal Schwann cell morphology	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:2176915	M	MP:0003871	abnormal myelin sheath morphology	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:2176915	M	MP:0003631	nervous system phenotype	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae * C57BL/6	Y	8790370
MGI:2176915	M	MP:0001262	decreased body weight	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae * C57BL/6	N	8790370
MGI:2176915	M	MP:0003632	abnormal nervous system morphology	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:2176915	M	MP:0005404	abnormal axon morphology	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:2176915	M	MP:0010400	increased liver glycogen level	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae * C57BL/6	N	8790370
MGI:2176915	M	MP:0005386	behavior/neurological phenotype	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae * C57BL/6	Y	9700485
MGI:2176915	M	MP:0000609	abnormal liver physiology	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae * C57BL/6	N	8790370
MGI:2177040	M	MP:0001147	small testis	Mei1<m1Jcs>/Mei1<m1Jcs>	involves: 129S1/Sv * C57BL/6J	N	10700192
MGI:2177040	F	MP:0001926	female infertility	Mei1<m1Jcs>/Mei1<m1Jcs>	involves: 129S1/Sv * C57BL/6J	N	10700192
MGI:2177040	F	MP:0005168	abnormal female meiosis	Mei1<m1Jcs>/Mei1<m1Jcs>	involves: 129S1/Sv * C57BL/6J	N	10700192
MGI:2177040	M	MP:0005159	azoospermia	Mei1<m1Jcs>/Mei1<m1Jcs>	involves: 129S1/Sv * C57BL/6J	N	10700192
MGI:2177040	M	MP:0008261	arrest of male meiosis	Mei1<m1Jcs>/Mei1<m1Jcs>	involves: 129S1/Sv * C57BL/6J	N	10700192
MGI:2177040	M	MP:0001925	male infertility	Mei1<m1Jcs>/Mei1<m1Jcs>	involves: 129S1/Sv * C57BL/6J	N	10700192
MGI:2177047	M	MP:0001925	male infertility	Dmc1<Mei11>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	N	10700192
MGI:2177047	M	MP:0001932	abnormal spermiogenesis	Dmc1<Mei11>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	N	10700192
MGI:2177047	M	MP:0002216	abnormal seminiferous tubule morphology	Dmc1<Mei11>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	N	10700192
MGI:2177047	M	MP:0004901	decreased male germ cell number	Dmc1<Mei11>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	N	10700192
MGI:2177048	M	MP:0001925	male infertility	rsph/rsph	involves: 129S4/SvJae * C57BL/6J	N	10700192
MGI:2177048	M	MP:0002686	globozoospermia	rsph/rsph	involves: 129S4/SvJae * C57BL/6J	N	10700192
MGI:2177295	F	MP:0002100	abnormal tooth morphology	Amelx<tm1Kul>/Amelx<tm1Kul>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11406633
MGI:2177295	F	MP:0000126	brittle teeth	Amelx<tm1Kul>/Amelx<tm1Kul>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11406633
MGI:2177295	F	MP:0002577	reduced enamel thickness	Amelx<tm1Kul>/Amelx<tm1Kul>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11406633
MGI:2177295	F	MP:0002649	abnormal enamel rod pattern	Amelx<tm1Kul>/Amelx<tm1Kul>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11406633
MGI:2177529	F	MP:0002637	small uterus	Cftr<tm1Unc>/Cftr<tm1Unc>	B6.129P2-Cftr<tm1Unc>/J	N	18325992
MGI:2177529	F	MP:0002680	decreased corpora lutea number	Cftr<tm1Unc>/Cftr<tm1Unc>	B6.129P2-Cftr<tm1Unc>/J	N	18325992
MGI:2177529	F	MP:0004905	decreased uterus weight	Cftr<tm1Unc>/Cftr<tm1Unc>	B6.129P2-Cftr<tm1Unc>/J	N	18325992
MGI:2177529	F	MP:0001135	abnormal uterine cervix morphology	Cftr<tm1Unc>/Cftr<tm1Unc>	B6.129P2-Cftr<tm1Unc>/J	N	18325992
MGI:2177529	F	MP:0009081	thin uterus	Cftr<tm1Unc>/Cftr<tm1Unc>	B6.129P2-Cftr<tm1Unc>/J	N	18325992
MGI:2177529	F	MP:0001127	small ovary	Cftr<tm1Unc>/Cftr<tm1Unc>	B6.129P2-Cftr<tm1Unc>/J	N	18325992
MGI:2177529	F	MP:0004856	decreased ovary weight	Cftr<tm1Unc>/Cftr<tm1Unc>	B6.129P2-Cftr<tm1Unc>/J	N	18325992
MGI:2177529	F	MP:0009006	prolonged estrous cycle	Cftr<tm1Unc>/Cftr<tm1Unc>	B6.129P2-Cftr<tm1Unc>/J	N	18325992
MGI:2177529	F	MP:0001923	reduced female fertility	Cftr<tm1Unc>/Cftr<tm1Unc>	B6.129P2-Cftr<tm1Unc>/J	N	18325992
MGI:2177529	F	MP:0001938	delayed sexual maturation	Cftr<tm1Unc>/Cftr<tm1Unc>	B6.129P2-Cftr<tm1Unc>/J	N	18325992
MGI:2177529	M	MP:0031012	impaired sperm migration in female genital tract	Cftr<tm1Unc>/Cftr<tm1Unc>	B6.129P2-Cftr<tm1Unc>/J	N	18325992
MGI:2177529	F	MP:0009009	absent estrous cycle	Cftr<tm1Unc>/Cftr<tm1Unc>	B6.129P2-Cftr<tm1Unc>/J	N	18325992
MGI:2177529	F	MP:0003355	decreased ovulation rate	Cftr<tm1Unc>/Cftr<tm1Unc>	B6.129P2-Cftr<tm1Unc>/J	N	18325992
MGI:2177530	F	MP:0001926	female infertility	Cftr<tm1Unc>/Cftr<tm1Unc>	involves: 129P2/OlaHsd	N	1380723
MGI:2177531	M	MP:0002769	abnormal vas deferens morphology	Cftr<tm1Hgu>/Cftr<tm1Hgu>	involves: 129P2/OlaHsd * MF1	N	1382232
MGI:2177541	F	MP:0001926	female infertility	Cftr<tm3Bay>/Cftr<tm3Bay>	involves: 129S7/SvEvBrd	N	7482032
MGI:2177552	F	MP:0001577	anemia	Gata1<tm1Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	8901585
MGI:2177552	F	MP:0005012	decreased eosinophil cell number	Gata1<tm1Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	12045237
MGI:2177553	M	MP:0000245	abnormal erythropoiesis	Gata1<tm1Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	8901585
MGI:2177553	M	MP:0001577	anemia	Gata1<tm1Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	8901585
MGI:2177553	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Gata1<tm1Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	8901585
MGI:2177556	F	MP:0001127	small ovary	Fshb<tm1Zuk>/Fshb<tm1Zuk>	either: 129S/SvEv or (involves: 129S7/SvEvBrd * C57BL/6)	N	9020850
MGI:2177556	F	MP:0001134	absent corpus luteum	Fshb<tm1Zuk>/Fshb<tm1Zuk>	either: 129S/SvEv or (involves: 129S7/SvEvBrd * C57BL/6)	N	9020850
MGI:2177556	F	MP:0001927	abnormal estrous cycle	Fshb<tm1Zuk>/Fshb<tm1Zuk>	either: 129S/SvEv or (involves: 129S7/SvEvBrd * C57BL/6)	N	9020850
MGI:2177556	F	MP:0002637	small uterus	Fshb<tm1Zuk>/Fshb<tm1Zuk>	either: 129S/SvEv or (involves: 129S7/SvEvBrd * C57BL/6)	N	9020850
MGI:2177556	F	MP:0001926	female infertility	Fshb<tm1Zuk>/Fshb<tm1Zuk>	either: 129S/SvEv or (involves: 129S7/SvEvBrd * C57BL/6)	N	9020850
MGI:2177556	M	MP:0001153	small seminiferous tubules	Fshb<tm1Zuk>/Fshb<tm1Zuk>	either: 129S/SvEv or (involves: 129S7/SvEvBrd * C57BL/6)	N	9020850
MGI:2177556	M	MP:0001147	small testis	Fshb<tm1Zuk>/Fshb<tm1Zuk>	either: 129S/SvEv or (involves: 129S7/SvEvBrd * C57BL/6)	N	9020850
MGI:2177556	M	MP:0002675	asthenozoospermia	Fshb<tm1Zuk>/Fshb<tm1Zuk>	either: 129S/SvEv or (involves: 129S7/SvEvBrd * C57BL/6)	N	9020850
MGI:2177556	F	MP:0001132	absent mature ovarian follicles	Fshb<tm1Zuk>/Fshb<tm1Zuk>	either: 129S/SvEv or (involves: 129S7/SvEvBrd * C57BL/6)	N	9020850
MGI:2177556	F	MP:0009009	absent estrous cycle	Fshb<tm1Zuk>/Fshb<tm1Zuk>	either: 129S/SvEv or (involves: 129S7/SvEvBrd * C57BL/6)	N	9020850
MGI:2177556	M	MP:0002687	oligozoospermia	Fshb<tm1Zuk>/Fshb<tm1Zuk>	either: 129S/SvEv or (involves: 129S7/SvEvBrd * C57BL/6)	N	9020850
MGI:2177556	F	MP:0001129	impaired ovarian folliculogenesis	Fshb<tm1Zuk>/Fshb<tm1Zuk>	either: 129S/SvEv or (involves: 129S7/SvEvBrd * C57BL/6)	N	9020850
MGI:2177657	M	MP:0001925	male infertility	Fus<tm1(DDIT3)Dron>/Fus<tm1(DDIT3)Dron>	involves: 129S6/SvEvTac * CD-1	N	10654943
MGI:2177657	M	MP:0005169	abnormal male meiosis	Fus<tm1(DDIT3)Dron>/Fus<tm1(DDIT3)Dron>	involves: 129S6/SvEvTac * CD-1	N	10654943
MGI:2177657	M	MP:0001147	small testis	Fus<tm1(DDIT3)Dron>/Fus<tm1(DDIT3)Dron>	involves: 129S6/SvEvTac * CD-1	N	10654943
MGI:2177657	F	MP:0001923	reduced female fertility	Fus<tm1(DDIT3)Dron>/Fus<tm1(DDIT3)Dron>	involves: 129S6/SvEvTac * CD-1	N	10654943
MGI:2177662	F	MP:0001923	reduced female fertility	Hmx3<tm1Tlu>/Hmx3<tm1Tlu>	involves: 129 * C57BL/6J	N	9435283
MGI:2177662	F	MP:0003845	abnormal decidualization	Hmx3<tm1Tlu>/Hmx3<tm1Tlu>	involves: 129 * C57BL/6J	N	9435283
MGI:2177662	F	MP:0001728	failure of embryo implantation	Hmx3<tm1Tlu>/Hmx3<tm1Tlu>	involves: 129 * C57BL/6J	N	9435283
MGI:2177663	F	MP:0003845	abnormal decidualization	Hmx3<tm2Tlu>/Hmx3<tm2Tlu>	involves: 129 * C57BL/6J	N	9435283
MGI:2177663	F	MP:0001923	reduced female fertility	Hmx3<tm2Tlu>/Hmx3<tm2Tlu>	involves: 129 * C57BL/6J	N	9435283
MGI:2177663	F	MP:0001728	failure of embryo implantation	Hmx3<tm2Tlu>/Hmx3<tm2Tlu>	involves: 129 * C57BL/6J	N	9435283
MGI:2177671	F	MP:0004834	ovary hemorrhage	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	M	MP:0006419	disorganized testis cords	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	F	MP:0001127	small ovary	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	F	MP:0002016	ovary cyst	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	F	MP:0005431	decreased oocyte number	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	M	MP:0013738	abnormal testis tunica albuginea morphology	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	F	MP:0009093	oocyte degeneration	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	F	MP:0001126	abnormal ovary morphology	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	F	MP:0001131	abnormal ovarian follicle morphology	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	F	MP:0013609	abnormal ovarian medulla morphology	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	F	MP:0013608	abnormal ovarian cortex morphology	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	F	MP:0001129	impaired ovarian folliculogenesis	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	F	MP:0013605	abnormal ovarian bursa morphology	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	M	MP:0001147	small testis	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	F	MP:0009071	short oviduct	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	F	MP:0009433	polyovular ovarian follicle	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177671	F	MP:0003574	abnormal oviduct morphology	Foxc1<tm1Blh>/Foxc1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	16412416
MGI:2177682	M	MP:0001925	male infertility	Brca1<tm2Arge>/Brca1<tm2Arge>	129-Brca1<tm2Arge>	N	11358863
MGI:2177682	M	MP:0001155	arrest of spermatogenesis	Brca1<tm2Arge>/Brca1<tm2Arge>	129-Brca1<tm2Arge>	N	11358863
MGI:2177683	M	MP:0001155	arrest of spermatogenesis	Brca1<tm2Arge>/Brca1<tm2Arge>	involves: 129/Sv * C57BL/6J * MF1	N	11358863
MGI:2177683	M	MP:0001925	male infertility	Brca1<tm2Arge>/Brca1<tm2Arge>	involves: 129/Sv * C57BL/6J * MF1	N	11358863
MGI:2177776	F	MP:0003845	abnormal decidualization	Il11ra1<tm1Gos>/Il11ra1<tm1Gos>	involves: 129S2/SvPas * C57BL/6J	N	9679067
MGI:2177776	F	MP:0001923	reduced female fertility	Il11ra1<tm1Gos>/Il11ra1<tm1Gos>	involves: 129S2/SvPas * C57BL/6J	N	9679067
MGI:2177776	F	MP:0001729	impaired embryo implantation	Il11ra1<tm1Gos>/Il11ra1<tm1Gos>	involves: 129S2/SvPas * C57BL/6J	N	9679067
MGI:2177777	F	MP:0001729	impaired embryo implantation	Il11ra1<tm2Gos>/Il11ra1<tm2Gos>	involves: 129S2/SvPas * C57BL/6J	N	9679067
MGI:2177777	F	MP:0003845	abnormal decidualization	Il11ra1<tm2Gos>/Il11ra1<tm2Gos>	involves: 129S2/SvPas * C57BL/6J	N	9679067
MGI:2177779	F	MP:0001926	female infertility	Il11ra1<tm1Wehi>/Il11ra1<tm1Wehi>	involves: 129S1/Sv * C57BL/6	N	9310465
MGI:2177779	F	MP:0001926	female infertility	Il11ra1<tm1Wehi>/Il11ra1<tm1Wehi>	involves: 129S1/Sv * C57BL/6	N	9500603
MGI:2177781	F	MP:0001926	female infertility	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv * C57BL/6J	N	1522892
MGI:2177781	F	MP:0001728	failure of embryo implantation	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv * C57BL/6J	N	1522892
MGI:2177781	F	MP:0001120	abnormal uterus morphology	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv * C57BL/6J	N	1522892
MGI:2177803	M	MP:0006428	ectopic Sertoli cells	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0004728	abnormal efferent ductules of testis morphology	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0020550	multinucleated giant male germ cells	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0002631	abnormal epididymis morphology	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0014052	increased male germ cell apoptosis	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0006379	abnormal spermatocyte morphology	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0001147	small testis	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0008261	arrest of male meiosis	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	9501026
MGI:2177803	M	MP:0001925	male infertility	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	9501026
MGI:2177803	M	MP:0001155	arrest of spermatogenesis	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0005159	azoospermia	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0001155	arrest of spermatogenesis	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	9501026
MGI:2177803	M	MP:0002216	abnormal seminiferous tubule morphology	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0005159	azoospermia	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	9501026
MGI:2177803	M	MP:0001146	abnormal testis morphology	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0004901	decreased male germ cell number	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0004852	decreased testis weight	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0020355	abnormal Sertoli cell barrier morphology	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	M	MP:0001925	male infertility	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	23727514
MGI:2177803	F	MP:0001926	female infertility	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	9501026
MGI:2177804	M	MP:0008261	arrest of male meiosis	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129/Sv * 129S2/SvPas	N	9501026
MGI:2177804	F	MP:0001926	female infertility	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129/Sv * 129S2/SvPas	N	9501026
MGI:2177804	M	MP:0001925	male infertility	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129/Sv * 129S2/SvPas	N	9501026
MGI:2177804	M	MP:0005159	azoospermia	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129/Sv * 129S2/SvPas	N	9501026
MGI:2177804	M	MP:0001156	abnormal spermatogenesis	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129/Sv * 129S2/SvPas	N	9501026
MGI:2177807	F	MP:0004014	abnormal uterine environment	Ptgs1<tm1Unc>/Ptgs1<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6	N	8521478
MGI:2177807	F	MP:0002907	abnormal parturition	Ptgs1<tm1Unc>/Ptgs1<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6	N	9751758
MGI:2177807	F	MP:0002679	abnormal corpus luteum morphology	Ptgs1<tm1Unc>/Ptgs1<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6	N	9751758
MGI:2177809	F	MP:0001134	absent corpus luteum	Ptgs2<tm1Jed>/Ptgs2<tm1Jed>	involves: 129S7/SvEvBrd	N	7477380
MGI:2177809	F	MP:0001926	female infertility	Ptgs2<tm1Jed>/Ptgs2<tm1Jed>	involves: 129S7/SvEvBrd	N	7477380
MGI:2177809	F	MP:0001127	small ovary	Ptgs2<tm1Jed>/Ptgs2<tm1Jed>	involves: 129S7/SvEvBrd	N	7477380
MGI:2177809	F	MP:0003355	decreased ovulation rate	Ptgs2<tm1Jed>/Ptgs2<tm1Jed>	involves: 129S7/SvEvBrd	N	7477380
MGI:2177811	F	MP:0031420	decreased superovulation rate	Ptgs2<tm1Unc>/Ptgs2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	10342859
MGI:2177811	F	MP:0009373	abnormal cumulus expansion	Ptgs2<tm1Unc>/Ptgs2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	10342859
MGI:2177811	F	MP:0002679	abnormal corpus luteum morphology	Ptgs2<tm1Unc>/Ptgs2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	10342859
MGI:2177811	F	MP:0001926	female infertility	Ptgs2<tm1Unc>/Ptgs2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	10342859
MGI:2177811	F	MP:0031422	failure of superovulation	Ptgs2<tm1Unc>/Ptgs2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	10342859
MGI:2177811	F	MP:0003357	impaired granulosa cell differentiation	Ptgs2<tm1Unc>/Ptgs2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	10342859
MGI:2177829	F	MP:0004014	abnormal uterine environment	Itgb3<tm1Hyn>/Itgb3<tm1Hyn>	involves: 129S2/SvPas * C57BL/6	N	9916135
MGI:2177829	F	MP:0001923	reduced female fertility	Itgb3<tm1Hyn>/Itgb3<tm1Hyn>	involves: 129S2/SvPas * C57BL/6	N	9916135
MGI:2177829	F	MP:0004898	uterine hemorrhage	Itgb3<tm1Hyn>/Itgb3<tm1Hyn>	involves: 129S2/SvPas * C57BL/6	N	9916135
MGI:2177829	F	MP:0031434	increased miscarriage rate	Itgb3<tm1Hyn>/Itgb3<tm1Hyn>	involves: 129S2/SvPas * C57BL/6	N	9916135
MGI:2177861	F	MP:0001923	reduced female fertility	Kmt2a<tm1Sjk>/Kmt2a<+>	involves: 129S2/SvPas * C3H * C57BL/6	N	7477409
MGI:2177946	F	MP:0006269	abnormal mammary gland growth during pregnancy	Pin1<tm1Tuc>/Pin1<tm1Tuc>	involves: 129P2/OlaHsd * C57BL/6	N	11805292
MGI:2177946	M	MP:0004852	decreased testis weight	Pin1<tm1Tuc>/Pin1<tm1Tuc>	involves: 129P2/OlaHsd * C57BL/6	N	11805292
MGI:2177946	M	MP:0001154	seminiferous tubule degeneration	Pin1<tm1Tuc>/Pin1<tm1Tuc>	involves: 129P2/OlaHsd * C57BL/6	N	11805292
MGI:2177946	M	MP:0005159	azoospermia	Pin1<tm1Tuc>/Pin1<tm1Tuc>	involves: 129P2/OlaHsd * C57BL/6	N	11805292
MGI:2178040	F	MP:0001923	reduced female fertility	Smarcad1<tm1Gos>/Smarcad1<tm1Gos>	involves: 129S2/SvPas * C57BL/6	N	10415348
MGI:2178040	F	MP:0005431	decreased oocyte number	Smarcad1<tm1Gos>/Smarcad1<tm1Gos>	involves: 129S2/SvPas * C57BL/6	N	10415348
MGI:2178040	M	MP:0001922	reduced male fertility	Smarcad1<tm1Gos>/Smarcad1<tm1Gos>	involves: 129S2/SvPas * C57BL/6	N	10415348
MGI:2178041	M	MP:0001922	reduced male fertility	Smarcad1<tm1Gos>/Smarcad1<tm1Gos>	129S2/SvPas-Smarcad1<tm1Gos>	N	10415348
MGI:2178041	F	MP:0005431	decreased oocyte number	Smarcad1<tm1Gos>/Smarcad1<tm1Gos>	129S2/SvPas-Smarcad1<tm1Gos>	N	10415348
MGI:2178041	F	MP:0001923	reduced female fertility	Smarcad1<tm1Gos>/Smarcad1<tm1Gos>	129S2/SvPas-Smarcad1<tm1Gos>	N	10415348
MGI:2178044	F	MP:0001923	reduced female fertility	Krt8<tm1Rgo>/Krt8<tm1Rgo>	involves: 129S2/SvPas * C57BL/6	N	7686525
MGI:2178096	M	MP:0001925	male infertility	Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>	either: (involves: 129S2/SvPas * 129/Sv) or (involves: 129S2/SvPas * C57BL/6)	N	8106170
MGI:2178117	M	MP:0005159	azoospermia	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>	involves: 129S2/SvPas * CF-1	N	7789268
MGI:2178117	M	MP:0002286	cryptorchism	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>	involves: 129S2/SvPas * CF-1	N	7789268
MGI:2178117	M	MP:0001156	abnormal spermatogenesis	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>	involves: 129S2/SvPas * CF-1	N	7789268
MGI:2178117	F	MP:0001926	female infertility	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>	involves: 129S2/SvPas * CF-1	N	7789268
MGI:2178117	M	MP:0009214	vas deferens hypoplasia	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>	involves: 129S2/SvPas * CF-1	N	7789268
MGI:2178117	M	MP:0002769	abnormal vas deferens morphology	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>	involves: 129S2/SvPas * CF-1	N	7789268
MGI:2178117	F	MP:0004014	abnormal uterine environment	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>	involves: 129S2/SvPas * CF-1	N	7789268
MGI:2178117	M	MP:0001925	male infertility	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>	involves: 129S2/SvPas * CF-1	N	7789268
MGI:2178117	M	MP:0001147	small testis	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>	involves: 129S2/SvPas * CF-1	N	7789268
MGI:2178117	M	MP:0014052	increased male germ cell apoptosis	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>	involves: 129S2/SvPas * CF-1	N	7789268
MGI:2178118	F	MP:0004014	abnormal uterine environment	Hoxa11<tm1Ssp>/Hoxa11<+>	involves: 129S2/SvPas * CF-1	N	7789268
MGI:2178745	M	MP:0003698	abnormal male reproductive system physiology	Hoxd10<tm1Mrc>/Hoxd10<tm1Mrc>	involves: 129S1/Sv * 129X1/SvJ	N	9409668
MGI:2178749	F	MP:0002066	abnormal motor capabilities/coordination/movement	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0001513	limb grasping	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0001417	decreased exploration in new environment	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0001405	impaired coordination	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0000947	convulsive seizures	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0002152	abnormal brain morphology	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0002757	decreased vertical activity	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0001393	ataxia	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0002064	seizures	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0002628	hepatic steatosis	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0004191	neuronal intranuclear inclusions	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0002083	premature death	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0000745	tremors	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0001406	abnormal gait	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178749	F	MP:0005424	jerky movement	Hprt1<tm1Detl>/Hprt1<tm1Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0003205	testicular atrophy	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0001417	decreased exploration in new environment	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0001393	ataxia	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0002628	hepatic steatosis	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0001406	abnormal gait	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0001513	limb grasping	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0001405	impaired coordination	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0005424	jerky movement	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0002757	decreased vertical activity	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0002152	abnormal brain morphology	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0002083	premature death	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0004191	neuronal intranuclear inclusions	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0000745	tremors	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0002066	abnormal motor capabilities/coordination/movement	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0001260	increased body weight	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0002064	seizures	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2178750	M	MP:0000947	convulsive seizures	Hprt1<tm1Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9413985
MGI:2179030	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm1Mak>/Pten<+>	involves: 129P2/OlaHsd * C57BL/6J	N	10910075
MGI:2179030	F	MP:0009092	endometrium hyperplasia	Pten<tm1Mak>/Pten<+>	involves: 129P2/OlaHsd * C57BL/6J	N	10910075
MGI:2179030	M	MP:0002216	abnormal seminiferous tubule morphology	Pten<tm1Mak>/Pten<+>	involves: 129P2/OlaHsd * C57BL/6J	N	9799734
MGI:2179030	F	MP:0004868	increased endometrial carcinoma incidence	Pten<tm1Mak>/Pten<+>	involves: 129P2/OlaHsd * C57BL/6J	N	10910075
MGI:2179045	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Rps>/Pten<+>	involves: 129S1/Sv * C57BL/6J	N	9990064
MGI:2179045	F	MP:0009092	endometrium hyperplasia	Pten<tm1Rps>/Pten<+>	involves: 129S1/Sv * C57BL/6J	N	9990064
MGI:2179553	F	MP:0001868	ovary inflammation	Relb<tm1Brv>/Relb<tm1Brv>	involves: 129S2/SvPas * C57BL/6	N	7834753
MGI:2179742	F	MP:0002169	no abnormal phenotype detected	Syp<tm1Sud>/Syp<tm1Sud>	involves: 129S1/Sv * 129X1/SvJ	N	8643476
MGI:2179821	F	MP:0005095	decreased T cell proliferation	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0008209	decreased pre-B cell number	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0008246	abnormal leukocyte morphology	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0008479	decreased spleen white pulp amount	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0002831	absent Peyer's patches	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0008211	decreased mature B cell number	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0001823	thymus hypoplasia	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0003850	abnormal thymocyte activation	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0002492	decreased IgE level	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0008046	absent NK cells	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0005018	decreased T cell number	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0001806	decreased IgM level	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0005070	impaired natural killer cell mediated cytotoxicity	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0008474	absent spleen germinal center	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0000694	spleen hypoplasia	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0002396	abnormal hematopoietic system morphology/development	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0004816	abnormal class switch recombination	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0008399	abnormal alpha-beta intraepithelial T cell morphology	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179821	F	MP:0008098	decreased plasma cell number	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0002492	decreased IgE level	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0008209	decreased pre-B cell number	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0004816	abnormal class switch recombination	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0001806	decreased IgM level	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0005018	decreased T cell number	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0001823	thymus hypoplasia	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	9334367
MGI:2179823	M	MP:0005070	impaired natural killer cell mediated cytotoxicity	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0008356	abnormal gamma-delta T cell differentiation	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	9334367
MGI:2179823	M	MP:0008046	absent NK cells	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0008348	absent gamma-delta T cells	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	9334367
MGI:2179823	M	MP:0008399	abnormal alpha-beta intraepithelial T cell morphology	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0005095	decreased T cell proliferation	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0008479	decreased spleen white pulp amount	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0008211	decreased mature B cell number	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0008246	abnormal leukocyte morphology	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0008352	absent gamma-delta intraepithelial T cell	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	9334367
MGI:2179823	M	MP:0001823	thymus hypoplasia	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0003850	abnormal thymocyte activation	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0002831	absent Peyer's patches	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0000694	spleen hypoplasia	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0008474	absent spleen germinal center	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2179823	M	MP:0008098	decreased plasma cell number	Il2rg<tm1Cgn>/Y	involves: 129 * CB20	N	7831294
MGI:2180049	F	MP:0006271	abnormal involution of the mammary gland	Il6<tm1Kopf>/Il6<tm1Kopf>	involves: 129S2/SvPas * C57BL/6	N	12456808
MGI:2180104	F	MP:0005158	ovary hypoplasia	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	M	MP:0002286	cryptorchism	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	F	MP:0008869	anovulation	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	M	MP:0009203	external male genitalia hypoplasia	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	M	MP:0009207	internal male genitalia hypoplasia	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	M	MP:0006380	abnormal spermatid morphology	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	M	MP:0001940	testis hypoplasia	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	F	MP:0001926	female infertility	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	M	MP:0002786	abnormal Leydig cell morphology	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	M	MP:0004901	decreased male germ cell number	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	M	MP:0005536	decreased Leydig cell number	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	M	MP:0001145	abnormal male reproductive system morphology	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	M	MP:0005148	seminal vesicle hypoplasia	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	M	MP:0001156	abnormal spermatogenesis	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	F	MP:0001119	abnormal female reproductive system morphology	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	F	MP:0001132	absent mature ovarian follicles	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	M	MP:0001925	male infertility	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	F	MP:0001121	uterus hypoplasia	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	F	MP:0001134	absent corpus luteum	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180104	M	MP:0005147	prostate gland hypoplasia	Nr5a1<tm2Klp>/Nr5a1<tm2.1Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11124111
MGI:2180121	F	MP:0001127	small ovary	Nr5a1<tm2Klp>/Nr5a1<tm2Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11416865
MGI:2180121	M	MP:0004852	decreased testis weight	Nr5a1<tm2Klp>/Nr5a1<tm2Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11416865
MGI:2180121	F	MP:0001926	female infertility	Nr5a1<tm2Klp>/Nr5a1<tm2Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11416865
MGI:2180121	M	MP:0001147	small testis	Nr5a1<tm2Klp>/Nr5a1<tm2Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11416865
MGI:2180121	M	MP:0005536	decreased Leydig cell number	Nr5a1<tm2Klp>/Nr5a1<tm2Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11416865
MGI:2180121	F	MP:0001121	uterus hypoplasia	Nr5a1<tm2Klp>/Nr5a1<tm2Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11416865
MGI:2180121	F	MP:0004856	decreased ovary weight	Nr5a1<tm2Klp>/Nr5a1<tm2Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11416865
MGI:2180121	M	MP:0005148	seminal vesicle hypoplasia	Nr5a1<tm2Klp>/Nr5a1<tm2Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11416865
MGI:2180121	F	MP:0001134	absent corpus luteum	Nr5a1<tm2Klp>/Nr5a1<tm2Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11416865
MGI:2180121	M	MP:0001925	male infertility	Nr5a1<tm2Klp>/Nr5a1<tm2Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11416865
MGI:2180121	F	MP:0001129	impaired ovarian folliculogenesis	Nr5a1<tm2Klp>/Nr5a1<tm2Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11416865
MGI:2180121	M	MP:0005147	prostate gland hypoplasia	Nr5a1<tm2Klp>/Nr5a1<tm2Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11416865
MGI:2180121	F	MP:0001132	absent mature ovarian follicles	Nr5a1<tm2Klp>/Nr5a1<tm2Klp>,Tg(Cga-cre)3Sac/0	involves: 129P2/OlaHsd * C57BL/6J * SJL	N	11416865
MGI:2180182	F	MP:0002293	long gestation period	Inhbb<tm1Jae>/Inhbb<tm1Jae>	either: (129S4/SvJae-Inhbb<tm1Jae>) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	N	8125256
MGI:2180182	F	MP:0000627	abnormal mammary gland morphology	Inhbb<tm1Jae>/Inhbb<tm1Jae>	either: (129S4/SvJae-Inhbb<tm1Jae>) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	N	8125256
MGI:2180182	F	MP:0013718	galactostasis	Inhbb<tm1Jae>/Inhbb<tm1Jae>	either: (129S4/SvJae-Inhbb<tm1Jae>) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	N	8125256
MGI:2180182	F	MP:0009505	abnormal mammary gland lobule morphology	Inhbb<tm1Jae>/Inhbb<tm1Jae>	either: (129S4/SvJae-Inhbb<tm1Jae>) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	N	8125256
MGI:2180182	F	MP:0001923	reduced female fertility	Inhbb<tm1Jae>/Inhbb<tm1Jae>	either: (129S4/SvJae-Inhbb<tm1Jae>) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	N	8125256
MGI:2180497	F	MP:0002920	decreased paired-pulse facilitation	Syngr1<tm1Sud>/Syngr1<tm1Sud>,Syp<tm1Sud>/Syp<tm1Sud>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	10595519
MGI:2180497	F	MP:0001473	reduced long-term potentiation	Syngr1<tm1Sud>/Syngr1<tm1Sud>,Syp<tm1Sud>/Syp<tm1Sud>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	10595519
MGI:2180497	F	MP:0002922	decreased post-tetanic potentiation	Syngr1<tm1Sud>/Syngr1<tm1Sud>,Syp<tm1Sud>/Syp<tm1Sud>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	10595519
MGI:2180497	F	MP:0001900	impaired synaptic plasticity	Syngr1<tm1Sud>/Syngr1<tm1Sud>,Syp<tm1Sud>/Syp<tm1Sud>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	10595519
MGI:2180519	F	MP:0009652	abnormal palatal rugae morphology	Eda<Ta>/Eda<Ta>	B6CBACa A<w-J>/A-Eda<Ta>/J-XO	N	18028050
MGI:2180831	M	MP:0010807	abnormal stomach position or orientation	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0010808	right-sided stomach	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0001685	abnormal endoderm development	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23303524
MGI:2180831	M	MP:0010402	ventricular septal defect	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0000284	double outlet right ventricle	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0004066	abnormal primitive node morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23303524
MGI:2180831	M	MP:0003984	embryonic growth retardation	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0004131	abnormal motile primary cilium morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23303524
MGI:2180831	M	MP:0000644	dextrocardia	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0000914	exencephaly	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0000269	abnormal heart looping	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0004252	abnormal direction of heart looping	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0011110	preweaning lethality, incomplete penetrance	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0004133	heterotaxia	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0000432	abnormal head morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0002766	situs inversus	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0006063	abnormal inferior vena cava morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0004158	right aortic arch	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0011091	prenatal lethality, complete penetrance	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	11959836
MGI:2180831	M	MP:0002151	abnormal neural tube morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0010854	lung situs inversus	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180831	M	MP:0000111	cleft palate	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0000269	abnormal heart looping	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0002766	situs inversus	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0004252	abnormal direction of heart looping	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0000929	open neural tube	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0000914	exencephaly	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0010403	atrial septal defect	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0010808	right-sided stomach	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0010807	abnormal stomach position or orientation	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0002151	abnormal neural tube morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0010853	abnormal lung position or orientation	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0000432	abnormal head morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0006065	abnormal heart position or orientation	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0003984	embryonic growth retardation	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0011110	preweaning lethality, incomplete penetrance	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0006063	abnormal inferior vena cava morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0004133	heterotaxia	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0000111	cleft palate	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180833	F	MP:0000644	dextrocardia	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd	N	23184148
MGI:2180884	F	MP:0008054	abnormal uterine NK cell morphology	Itgb7<tm1Cgn>/Itgb7<tm1Cgn>	involves: C57BL/6	N	9421796
MGI:2180884	F	MP:0008256	abnormal myometrium morphology	Itgb7<tm1Cgn>/Itgb7<tm1Cgn>	involves: C57BL/6	N	9421796
MGI:2180884	F	MP:0009394	increased uterine NK cell number	Itgb7<tm1Cgn>/Itgb7<tm1Cgn>	involves: C57BL/6	N	9421796
MGI:2181410	M	MP:0001147	small testis	Crem<tm1Gsc>/Crem<tm1Gsc>	involves: 129 * C57BL/6	N	8600391
MGI:2181410	M	MP:0008261	arrest of male meiosis	Crem<tm1Gsc>/Crem<tm1Gsc>	involves: 129 * C57BL/6	N	8600391
MGI:2181410	M	MP:0001925	male infertility	Crem<tm1Gsc>/Crem<tm1Gsc>	involves: 129 * C57BL/6	N	8600391
MGI:2181413	M	MP:0001153	small seminiferous tubules	Crem<tm1Saco>/Crem<tm1Saco>	involves: 129/Sv * C57BL/6	N	8600390
MGI:2181413	M	MP:0020550	multinucleated giant male germ cells	Crem<tm1Saco>/Crem<tm1Saco>	involves: 129/Sv * C57BL/6	N	9851970
MGI:2181413	M	MP:0001925	male infertility	Crem<tm1Saco>/Crem<tm1Saco>	involves: 129/Sv * C57BL/6	N	8600390
MGI:2181413	M	MP:0004852	decreased testis weight	Crem<tm1Saco>/Crem<tm1Saco>	involves: 129/Sv * C57BL/6	N	8600390
MGI:2181413	M	MP:0001155	arrest of spermatogenesis	Crem<tm1Saco>/Crem<tm1Saco>	involves: 129/Sv * C57BL/6	N	8600390
MGI:2181617	M	MP:0009201	external male genitalia atrophy	Kl<kl>/Kl<kl>	either: C.Cg-Kl<kl> or (involves: C3H/HeJ * C57BL/6J)	N	9363890
MGI:2181617	M	MP:0002216	abnormal seminiferous tubule morphology	Kl<kl>/Kl<kl>	either: C.Cg-Kl<kl> or (involves: C3H/HeJ * C57BL/6J)	N	9363890
MGI:2181617	F	MP:0004894	uterus atrophy	Kl<kl>/Kl<kl>	either: C.Cg-Kl<kl> or (involves: C3H/HeJ * C57BL/6J)	N	9363890
MGI:2181617	M	MP:0005159	azoospermia	Kl<kl>/Kl<kl>	either: C.Cg-Kl<kl> or (involves: C3H/HeJ * C57BL/6J)	N	9363890
MGI:2181617	F	MP:0004833	ovary atrophy	Kl<kl>/Kl<kl>	either: C.Cg-Kl<kl> or (involves: C3H/HeJ * C57BL/6J)	N	9363890
MGI:2181617	F	MP:0009212	vulva atrophy	Kl<kl>/Kl<kl>	either: C.Cg-Kl<kl> or (involves: C3H/HeJ * C57BL/6J)	N	9363890
MGI:2181617	M	MP:0008261	arrest of male meiosis	Kl<kl>/Kl<kl>	either: C.Cg-Kl<kl> or (involves: C3H/HeJ * C57BL/6J)	N	9363890
MGI:2181617	M	MP:0003205	testicular atrophy	Kl<kl>/Kl<kl>	either: C.Cg-Kl<kl> or (involves: C3H/HeJ * C57BL/6J)	N	9363890
MGI:2181617	F	MP:0001132	absent mature ovarian follicles	Kl<kl>/Kl<kl>	either: C.Cg-Kl<kl> or (involves: C3H/HeJ * C57BL/6J)	N	9363890
MGI:2181697	F	MP:0000628	abnormal mammary gland development	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	N	9988269
MGI:2181697	F	MP:0002682	decreased mature ovarian follicle number	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	N	9988269
MGI:2181697	F	MP:0001131	abnormal ovarian follicle morphology	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	N	9988269
MGI:2181697	F	MP:0001134	absent corpus luteum	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	N	9988269
MGI:2181697	F	MP:0001926	female infertility	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	N	9988269
MGI:2181697	F	MP:0009009	absent estrous cycle	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	N	9988269
MGI:2181697	F	MP:0001129	impaired ovarian folliculogenesis	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	N	9988269
MGI:2181697	F	MP:0009733	absent nipple	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	N	9988269
MGI:2181697	F	MP:0001119	abnormal female reproductive system morphology	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	N	9988269
MGI:2181697	F	MP:0008000	increased ovary tumor incidence	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	N	9988269
MGI:2181772	M	MP:0006415	absent testes	Lhx1<tm1Bhr>/Lhx1<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	7700351
MGI:2181772	F	MP:0003578	absent ovary	Lhx1<tm1Bhr>/Lhx1<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	7700351
MGI:2181774	M	MP:0006380	abnormal spermatid morphology	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	N	11389091
MGI:2181774	M	MP:0001154	seminiferous tubule degeneration	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	N	11389091
MGI:2181774	F	MP:0001931	abnormal oogenesis	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	N	11389091
MGI:2181774	M	MP:0003830	abnormal testis development	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	N	11389091
MGI:2181774	M	MP:0001156	abnormal spermatogenesis	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	N	11389091
MGI:2181774	M	MP:0006379	abnormal spermatocyte morphology	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	N	11389091
MGI:2181825	F	MP:0004895	vagina atrophy	Lhx9<tm1Lmgd>/Lhx9<tm1Lmgd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10706291
MGI:2181825	F	MP:0004894	uterus atrophy	Lhx9<tm1Lmgd>/Lhx9<tm1Lmgd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10706291
MGI:2181825	F	MP:0009009	absent estrous cycle	Lhx9<tm1Lmgd>/Lhx9<tm1Lmgd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10706291
MGI:2181825	M	MP:0002780	decreased circulating testosterone level	Lhx9<tm1Lmgd>/Lhx9<tm1Lmgd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10706291
MGI:2181825	F	MP:0001119	abnormal female reproductive system morphology	Lhx9<tm1Lmgd>/Lhx9<tm1Lmgd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10706291
MGI:2181825	M	MP:0006415	absent testes	Lhx9<tm1Lmgd>/Lhx9<tm1Lmgd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10706291
MGI:2181825	M	MP:0001145	abnormal male reproductive system morphology	Lhx9<tm1Lmgd>/Lhx9<tm1Lmgd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10706291
MGI:2181825	F	MP:0001750	increased circulating follicle stimulating hormone level	Lhx9<tm1Lmgd>/Lhx9<tm1Lmgd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10706291
MGI:2181825	F	MP:0005181	decreased circulating estradiol level	Lhx9<tm1Lmgd>/Lhx9<tm1Lmgd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10706291
MGI:2181825	M	MP:0001925	male infertility	Lhx9<tm1Lmgd>/Lhx9<tm1Lmgd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10706291
MGI:2181825	F	MP:0001926	female infertility	Lhx9<tm1Lmgd>/Lhx9<tm1Lmgd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10706291
MGI:2181825	F	MP:0003578	absent ovary	Lhx9<tm1Lmgd>/Lhx9<tm1Lmgd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10706291
MGI:2182003	F	MP:0009081	thin uterus	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	F	MP:0001132	absent mature ovarian follicles	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	F	MP:0001129	impaired ovarian folliculogenesis	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0000671	bulbourethral gland hypoplasia	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0000664	small prostate gland anterior lobe	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	F	MP:0001134	absent corpus luteum	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0001153	small seminiferous tubules	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0001153	small seminiferous tubules	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0004543	abnormal sperm physiology	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	F	MP:0014270	decreased ovary secretion	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0014269	decreased testes secretion	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0001145	abnormal male reproductive system morphology	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	F	MP:0001119	abnormal female reproductive system morphology	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0004852	decreased testis weight	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0004852	decreased testis weight	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0002566	abnormal sexual interaction	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	F	MP:0009021	absent estrus	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0001155	arrest of spermatogenesis	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0001155	arrest of spermatogenesis	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0001922	reduced male fertility	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0003611	scrotum hypoplasia	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0003611	scrotum hypoplasia	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0003608	prostate gland inflammation	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0002785	absent Leydig cells	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0001158	abnormal prostate gland morphology	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0001147	small testis	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0005536	decreased Leydig cell number	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0005536	decreased Leydig cell number	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	F	MP:0001127	small ovary	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0002286	cryptorchism	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0002286	cryptorchism	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0002660	abnormal caput epididymis morphology	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0005188	small penis	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0005188	small penis	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0001925	male infertility	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	F	MP:0009088	thin uterine horn	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0002687	oligozoospermia	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	F	MP:0001120	abnormal uterus morphology	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0005147	prostate gland hypoplasia	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	F	MP:0009009	absent estrous cycle	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0001157	small seminal vesicle	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0004932	epididymis hypoplasia	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0005148	seminal vesicle hypoplasia	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	M	MP:0009214	vas deferens hypoplasia	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0009201	external male genitalia atrophy	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	M	MP:0001378	abnormal ejaculation	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	15514086
MGI:2182003	F	MP:0001926	female infertility	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182003	F	MP:0009097	absent endometrial glands	Lhcgr<tm1Hht>/Lhcgr<tm1Hht>	involves: 129S7/SvEvBrd * C57BL/6J	N	11145748
MGI:2182004	F	MP:0009096	decreased endometrial gland number	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	F	MP:0031379	ambiguous external female genitalia	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	F	MP:0003531	abnormal vagina development	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0002660	abnormal caput epididymis morphology	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	12604639
MGI:2182004	M	MP:0004930	small epididymis	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0013604	abnormal adult Leydig cell differentiation	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0001157	small seminal vesicle	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0002662	abnormal cauda epididymis morphology	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	12604639
MGI:2182004	F	MP:0001120	abnormal uterus morphology	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	F	MP:0009081	thin uterus	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0004852	decreased testis weight	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0001155	arrest of spermatogenesis	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0014193	decreased epididymal cell proliferation	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	12604639
MGI:2182004	F	MP:0001132	absent mature ovarian follicles	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0004910	decreased seminal vesicle weight	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0002631	abnormal epididymis morphology	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	12604639
MGI:2182004	M	MP:0002774	small prostate gland	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0002216	abnormal seminiferous tubule morphology	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	F	MP:0001134	absent corpus luteum	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0005188	small penis	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0002286	cryptorchism	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	F	MP:0001127	small ovary	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	F	MP:0008257	thin myometrium	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0001153	small seminiferous tubules	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	F	MP:0001926	female infertility	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	F	MP:0001142	abnormal vagina orifice morphology	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0001925	male infertility	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0005536	decreased Leydig cell number	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	F	MP:0008258	thin endometrium	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0004929	decreased epididymis weight	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0001940	testis hypoplasia	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	F	MP:0001119	abnormal female reproductive system morphology	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0004932	epididymis hypoplasia	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0005148	seminal vesicle hypoplasia	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	F	MP:0001126	abnormal ovary morphology	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0014052	increased male germ cell apoptosis	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	12604639
MGI:2182004	F	MP:0001129	impaired ovarian folliculogenesis	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0004933	abnormal epididymis epithelium morphology	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	12604639
MGI:2182004	F	MP:0009009	absent estrous cycle	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	F	MP:0004856	decreased ovary weight	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182004	M	MP:0005147	prostate gland hypoplasia	Lhcgr<tm1Zmlei>/Lhcgr<tm1Zmlei>	either: 129X1/SvJ-Lhcgr<tm1Zmlei> or (involves: 129X1/SvJ * C57BL/6)	N	11145749
MGI:2182097	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Lrp8<tm1Her>/Lrp8<tm1Her>	involves: 129S6/SvEvTac	N	12695510
MGI:2182097	M	MP:0001925	male infertility	Lrp8<tm1Her>/Lrp8<tm1Her>	involves: 129S6/SvEvTac	N	12695510
MGI:2182097	M	MP:0008892	abnormal sperm flagellum morphology	Lrp8<tm1Her>/Lrp8<tm1Her>	involves: 129S6/SvEvTac	N	12695510
MGI:2182097	M	MP:0009238	coiled sperm flagellum	Lrp8<tm1Her>/Lrp8<tm1Her>	involves: 129S6/SvEvTac	N	12695510
MGI:2182097	M	MP:0002675	asthenozoospermia	Lrp8<tm1Her>/Lrp8<tm1Her>	involves: 129S6/SvEvTac	N	12695510
MGI:2182097	M	MP:0009831	abnormal sperm midpiece morphology	Lrp8<tm1Her>/Lrp8<tm1Her>	involves: 129S6/SvEvTac	N	12695510
MGI:2182097	M	MP:0001925	male infertility	Lrp8<tm1Her>/Lrp8<tm1Her>	involves: 129S6/SvEvTac	N	10380922
MGI:2182097	M	MP:0009243	hairpin sperm flagellum	Lrp8<tm1Her>/Lrp8<tm1Her>	involves: 129S6/SvEvTac	N	12695510
MGI:2182097	M	MP:0009237	kinked sperm flagellum	Lrp8<tm1Her>/Lrp8<tm1Her>	involves: 129S6/SvEvTac	N	12695510
MGI:2182097	M	MP:0004543	abnormal sperm physiology	Lrp8<tm1Her>/Lrp8<tm1Her>	involves: 129S6/SvEvTac	N	12695510
MGI:2182097	M	MP:0001156	abnormal spermatogenesis	Lrp8<tm1Her>/Lrp8<tm1Her>	involves: 129S6/SvEvTac	N	12695510
MGI:2182107	M	MP:0001925	male infertility	B4galnt1<tm1Rlp>/B4galnt1<tm1Rlp>	involves: 129S6/SvEvTac * C57BL/6	N	10021458
MGI:2182107	M	MP:0001154	seminiferous tubule degeneration	B4galnt1<tm1Rlp>/B4galnt1<tm1Rlp>	involves: 129S6/SvEvTac * C57BL/6	N	10021458
MGI:2182124	F	MP:0001923	reduced female fertility	Myc<tm1Brd>/Myc<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	8458579
MGI:2182343	F	MP:0003575	absent oviduct	Emx2<tm1Sia>/Emx2<tm1Sia>	involves: C57BL/6 * CBA	N	9165114
MGI:2182343	F	MP:0009210	absent internal female genitalia	Emx2<tm1Sia>/Emx2<tm1Sia>	involves: C57BL/6 * CBA	N	9165114
MGI:2182343	M	MP:0004729	absent efferent ductules of testis	Emx2<tm1Sia>/Emx2<tm1Sia>	involves: C57BL/6 * CBA	N	9165114
MGI:2182343	M	MP:0003642	absent seminal vesicle	Emx2<tm1Sia>/Emx2<tm1Sia>	involves: C57BL/6 * CBA	N	9165114
MGI:2182343	M	MP:0004727	absent epididymis	Emx2<tm1Sia>/Emx2<tm1Sia>	involves: C57BL/6 * CBA	N	9165114
MGI:2182343	M	MP:0003557	absent vas deferens	Emx2<tm1Sia>/Emx2<tm1Sia>	involves: C57BL/6 * CBA	N	9165114
MGI:2182343	M	MP:0009206	absent internal male genitalia	Emx2<tm1Sia>/Emx2<tm1Sia>	involves: C57BL/6 * CBA	N	9165114
MGI:2182343	F	MP:0003578	absent ovary	Emx2<tm1Sia>/Emx2<tm1Sia>	involves: C57BL/6 * CBA	N	9165114
MGI:2182343	F	MP:0003558	absent uterus	Emx2<tm1Sia>/Emx2<tm1Sia>	involves: C57BL/6 * CBA	N	9165114
MGI:2182343	M	MP:0006415	absent testes	Emx2<tm1Sia>/Emx2<tm1Sia>	involves: C57BL/6 * CBA	N	9165114
MGI:2182343	F	MP:0009072	absent cranial vagina	Emx2<tm1Sia>/Emx2<tm1Sia>	involves: C57BL/6 * CBA	N	9165114
MGI:2182709	M	MP:0002675	asthenozoospermia	Zbtb16<tm1Ppp>/Zbtb16<tm1Ppp>	involves: 129S1/Sv	N	15156143
MGI:2182709	M	MP:0003205	testicular atrophy	Zbtb16<tm1Ppp>/Zbtb16<tm1Ppp>	involves: 129S1/Sv	N	15156143
MGI:2182709	M	MP:0002685	abnormal spermatogonia proliferation	Zbtb16<tm1Ppp>/Zbtb16<tm1Ppp>	involves: 129S1/Sv	N	15156143
MGI:2182709	M	MP:0001156	abnormal spermatogenesis	Zbtb16<tm1Ppp>/Zbtb16<tm1Ppp>	involves: 129S1/Sv	N	15156143
MGI:2182709	M	MP:0001154	seminiferous tubule degeneration	Zbtb16<tm1Ppp>/Zbtb16<tm1Ppp>	involves: 129S1/Sv	N	15156143
MGI:2182709	M	MP:0006378	abnormal spermatogonia morphology	Zbtb16<tm1Ppp>/Zbtb16<tm1Ppp>	involves: 129S1/Sv	N	15156143
MGI:2182709	M	MP:0001147	small testis	Zbtb16<tm1Ppp>/Zbtb16<tm1Ppp>	involves: 129S1/Sv	N	15156143
MGI:2182709	M	MP:0002687	oligozoospermia	Zbtb16<tm1Ppp>/Zbtb16<tm1Ppp>	involves: 129S1/Sv	N	15156143
MGI:2182709	M	MP:0014052	increased male germ cell apoptosis	Zbtb16<tm1Ppp>/Zbtb16<tm1Ppp>	involves: 129S1/Sv	N	15156143
MGI:2182709	M	MP:0001152	increased Leydig cell number	Zbtb16<tm1Ppp>/Zbtb16<tm1Ppp>	involves: 129S1/Sv	N	15156143
MGI:2183214	M	MP:0001147	small testis	Cenpb<tm1Khac>/Cenpb<tm1Khac>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9548711
MGI:2183214	M	MP:0002687	oligozoospermia	Cenpb<tm1Khac>/Cenpb<tm1Khac>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9548711
MGI:2183214	F	MP:0004014	abnormal uterine environment	Cenpb<tm1Khac>/Cenpb<tm1Khac>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10645947
MGI:2183214	F	MP:0001120	abnormal uterus morphology	Cenpb<tm1Khac>/Cenpb<tm1Khac>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10645947
MGI:2183214	F	MP:0001923	reduced female fertility	Cenpb<tm1Khac>/Cenpb<tm1Khac>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10645947
MGI:2183304	F	MP:0012736	abnormal polar body morphology	Mos<tm1Ev>/Mos<tm1Ev>	involves: 129S/SvEv	N	8015609
MGI:2183304	M	MP:0005389	reproductive system phenotype	Mos<tm1Ev>/Mos<tm1Ev>	involves: 129S/SvEv	Y	12112586
MGI:2183304	F	MP:0001923	reduced female fertility	Mos<tm1Ev>/Mos<tm1Ev>	involves: 129S/SvEv	N	8015609
MGI:2183304	F	MP:0002016	ovary cyst	Mos<tm1Ev>/Mos<tm1Ev>	involves: 129S/SvEv	N	8015609
MGI:2183304	F	MP:0005168	abnormal female meiosis	Mos<tm1Ev>/Mos<tm1Ev>	involves: 129S/SvEv	N	8015609
MGI:2183396	M	MP:0005159	azoospermia	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	N	9916805
MGI:2183396	M	MP:0005169	abnormal male meiosis	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	N	10809667
MGI:2183396	F	MP:0001926	female infertility	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	N	9916805
MGI:2183396	M	MP:0001925	male infertility	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	N	9916805
MGI:2183396	F	MP:0005168	abnormal female meiosis	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	N	9916805
MGI:2183396	F	MP:0002016	ovary cyst	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	N	9916805
MGI:2183396	M	MP:0001147	small testis	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	N	9916805
MGI:2183396	M	MP:0005169	abnormal male meiosis	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	N	9916805
MGI:2183396	F	MP:0013236	ovary degeneration	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	N	9916805
MGI:2183396	F	MP:0005431	decreased oocyte number	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	N	9916805
MGI:2183396	F	MP:0013605	abnormal ovarian bursa morphology	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	N	9916805
MGI:2183938	M	MP:0005330	cardiomyopathy	Gla<tm1Kul>/Y	involves: 129S4/SvJae * C57BL/6	N	22574107
MGI:2183938	M	MP:0000598	abnormal liver morphology	Gla<tm1Kul>/Y	involves: 129S4/SvJae * C57BL/6	N	9122231
MGI:2183938	M	MP:0006264	decreased systemic arterial systolic blood pressure	Gla<tm1Kul>/Y	involves: 129S4/SvJae * C57BL/6	N	22574107
MGI:2183938	M	MP:0001636	irregular heartbeat	Gla<tm1Kul>/Y	involves: 129S4/SvJae * C57BL/6	N	22574107
MGI:2183938	M	MP:0002625	heart left ventricle hypertrophy	Gla<tm1Kul>/Y	involves: 129S4/SvJae * C57BL/6	N	22574107
MGI:2183938	M	MP:0002135	abnormal kidney morphology	Gla<tm1Kul>/Y	involves: 129S4/SvJae * C57BL/6	N	9122231
MGI:2183938	M	MP:0000358	abnormal cell morphology	Gla<tm1Kul>/Y	involves: 129S4/SvJae * C57BL/6	N	9122231
MGI:2183938	M	MP:0001544	abnormal cardiovascular system physiology	Gla<tm1Kul>/Y	involves: 129S4/SvJae * C57BL/6	N	22574107
MGI:2183938	M	MP:0002833	increased heart weight	Gla<tm1Kul>/Y	involves: 129S4/SvJae * C57BL/6	N	22574107
MGI:2183938	M	MP:0010574	dilated aorta	Gla<tm1Kul>/Y	involves: 129S4/SvJae * C57BL/6	N	22574107
MGI:2183938	M	MP:0005333	decreased heart rate	Gla<tm1Kul>/Y	involves: 129S4/SvJae * C57BL/6	N	22574107
MGI:2183938	M	MP:0010506	prolonged RR interval	Gla<tm1Kul>/Y	involves: 129S4/SvJae * C57BL/6	N	22574107
MGI:2384276	M	MP:0001925	male infertility	Morc1<Tg(Tyr)1Az>/Morc1<Tg(Tyr)1Az>	FVB/NHsd-Morc1<Tg(Tyr)1Az>	N	9826705
MGI:2384276	M	MP:0001147	small testis	Morc1<Tg(Tyr)1Az>/Morc1<Tg(Tyr)1Az>	FVB/NHsd-Morc1<Tg(Tyr)1Az>	N	9826705
MGI:2384276	M	MP:0004901	decreased male germ cell number	Morc1<Tg(Tyr)1Az>/Morc1<Tg(Tyr)1Az>	FVB/NHsd-Morc1<Tg(Tyr)1Az>	N	9826705
MGI:2384276	M	MP:0005159	azoospermia	Morc1<Tg(Tyr)1Az>/Morc1<Tg(Tyr)1Az>	FVB/NHsd-Morc1<Tg(Tyr)1Az>	N	9826705
MGI:2384276	M	MP:0008261	arrest of male meiosis	Morc1<Tg(Tyr)1Az>/Morc1<Tg(Tyr)1Az>	FVB/NHsd-Morc1<Tg(Tyr)1Az>	N	9826705
MGI:2384396	F	MP:0013718	galactostasis	Foxb1<tm1Blh>/Foxb1<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	9118797
MGI:2384398	F	MP:0001382	abnormal nursing	Foxb1<tm1Pgr>/Foxb1<tm1Pgr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9409663
MGI:2384398	F	MP:0001386	abnormal maternal nurturing	Foxb1<tm1Pgr>/Foxb1<tm1Pgr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9409663
MGI:2386444	F	MP:0001923	reduced female fertility	Ercc2<tm2(ERCC2)Jhjh>/Ercc2<tm2(ERCC2)Jhjh>	involves: 129P2/OlaHsd * C57BL/6	N	11950998
MGI:2386444	F	MP:0001928	abnormal ovulation	Ercc2<tm2(ERCC2)Jhjh>/Ercc2<tm2(ERCC2)Jhjh>	involves: 129P2/OlaHsd * C57BL/6	N	11950998
MGI:2386444	F	MP:0001923	reduced female fertility	Ercc2<tm2(ERCC2)Jhjh>/Ercc2<tm2(ERCC2)Jhjh>	involves: 129P2/OlaHsd * C57BL/6	N	9651581
MGI:2386738	M	MP:0005578	teratozoospermia	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	16850391
MGI:2386738	F	MP:0009096	decreased endometrial gland number	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0031381	decreased secondary ovarian follicle number	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0008257	thin myometrium	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0009363	abnormal tertiary ovarian follicle morphology	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0001926	female infertility	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0004894	uterus atrophy	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	M	MP:0004543	abnormal sperm physiology	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	16850391
MGI:2386738	F	MP:0011129	decreased tertiary ovarian follicle number	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0008869	anovulation	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0008258	thin endometrium	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0001127	small ovary	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0001131	abnormal ovarian follicle morphology	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0008868	abnormal granulosa cell morphology	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0001134	absent corpus luteum	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0009081	thin uterus	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	M	MP:0002687	oligozoospermia	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	16850391
MGI:2386738	M	MP:0009230	abnormal sperm head morphology	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	16850391
MGI:2386738	M	MP:0001154	seminiferous tubule degeneration	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	16850391
MGI:2386738	M	MP:0001155	arrest of spermatogenesis	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	16850391
MGI:2386738	M	MP:0009234	absent sperm head	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	16850391
MGI:2386738	F	MP:0031420	decreased superovulation rate	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0014270	decreased ovary secretion	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	M	MP:0008545	absent sperm flagellum	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	16850391
MGI:2386738	F	MP:0009009	absent estrous cycle	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0001126	abnormal ovary morphology	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0004856	decreased ovary weight	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0001119	abnormal female reproductive system morphology	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	M	MP:0030978	impaired binding of sperm to zona pellucida	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	16850391
MGI:2386738	F	MP:0001132	absent mature ovarian follicles	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	F	MP:0009359	endometrium atrophy	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	15105438
MGI:2386738	M	MP:0001925	male infertility	Npc1<m1N>/Npc1<m1N>	involves: BALB/c	N	16850391
MGI:2386740	F	MP:0001386	abnormal maternal nurturing	Abcb1a<tm1Bor>/Abcb1a<tm1Bor>,Npc1<m1N>/Npc1<m1N>	involves: 129/Ola * BALB/c	N	11984826
MGI:2386959	M	MP:0005536	decreased Leydig cell number	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386959	F	MP:0001119	abnormal female reproductive system morphology	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386959	M	MP:0004852	decreased testis weight	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386959	M	MP:0002784	abnormal Sertoli cell morphology	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386959	M	MP:0003698	abnormal male reproductive system physiology	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386959	F	MP:0002679	abnormal corpus luteum morphology	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386959	M	MP:0002216	abnormal seminiferous tubule morphology	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386959	F	MP:0001926	female infertility	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386959	M	MP:0001145	abnormal male reproductive system morphology	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386959	F	MP:0003699	abnormal female reproductive system physiology	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386959	M	MP:0002687	oligozoospermia	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386959	F	MP:0031419	delayed estrus	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386959	F	MP:0001127	small ovary	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386959	M	MP:0001922	reduced male fertility	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2386971	M	MP:0001152	increased Leydig cell number	Cdk4<tm1.1Bbd>/Cdk4<tm1.1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	10319860
MGI:2387312	M	MP:0005159	azoospermia	Rhbdf2<Uncv>/Rhbdf2<Uncv>	involves: BALB/c	N	10425919
MGI:2387325	F	MP:0008513	thin retina inner plexiform layer	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0003222	increased cardiomyocyte apoptosis	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387325	F	MP:0001625	cardiac hypertrophy	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387325	F	MP:0004215	abnormal myocardial fiber physiology	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387325	F	MP:0008519	thin retina outer plexiform layer	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0001262	decreased body weight	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387325	F	MP:0031606	increased susceptibility to age-related retinal degeneration	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0008067	retina ganglion cell degeneration	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0008103	amacrine cell degeneration	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0000416	sparse hair	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387325	F	MP:0002127	abnormal cardiovascular system morphology	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387325	F	MP:0003077	abnormal cell cycle	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0001265	decreased body size	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387325	F	MP:0001544	abnormal cardiovascular system physiology	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387325	F	MP:0004098	abnormal cerebellar granule cell morphology	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0004097	abnormal cerebellar cortex morphology	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0000876	Purkinje cell degeneration	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387325	F	MP:0000876	Purkinje cell degeneration	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0002066	abnormal motor capabilities/coordination/movement	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387325	F	MP:0011593	increased catalase activity	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0011593	increased catalase activity	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387325	F	MP:0008406	increased cellular sensitivity to hydrogen peroxide	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0010955	abnormal respiratory electron transport chain	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387325	F	MP:0003674	oxidative stress	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0003674	oxidative stress	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387325	F	MP:0008236	decreased susceptibility to neuronal excitotoxicity	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15703386
MGI:2387325	F	MP:0009763	increased susceptibility to induced morbidity/mortality	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387325	F	MP:0000745	tremors	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387325	F	MP:0001405	impaired coordination	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387325	F	MP:0012660	increased superoxide dismutase level	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387325	F	MP:0001406	abnormal gait	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387325	F	MP:0001393	ataxia	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387325	F	MP:0001333	absent optic nerve	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387325	F	MP:0001393	ataxia	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387325	F	MP:0000950	abnormal seizure response to pharmacological agent	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15703386
MGI:2387325	F	MP:0000414	alopecia	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387325	F	MP:0002083	premature death	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387325	F	MP:0000886	abnormal cerebellar granule layer morphology	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387325	F	MP:0000886	abnormal cerebellar granule layer morphology	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0000852	small cerebellum	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0005140	decreased cardiac muscle contractility	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387325	F	MP:0009674	decreased birth weight	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387325	F	MP:0000343	abnormal response to cardiac infarction	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387325	F	MP:0002753	dilated heart left ventricle	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387325	F	MP:0005551	abnormal eye electrophysiology	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387325	F	MP:0003037	increased myocardial infarct size	Aifm1<Hq>/Aifm1<Hq>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387326	M	MP:0004098	abnormal cerebellar granule cell morphology	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0000852	small cerebellum	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0010955	abnormal respiratory electron transport chain	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387326	M	MP:0003077	abnormal cell cycle	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0002127	abnormal cardiovascular system morphology	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387326	M	MP:0003037	increased myocardial infarct size	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387326	M	MP:0008513	thin retina inner plexiform layer	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0005551	abnormal eye electrophysiology	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0000876	Purkinje cell degeneration	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0000414	alopecia	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387326	M	MP:0000876	Purkinje cell degeneration	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387326	M	MP:0001262	decreased body weight	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387326	M	MP:0008103	amacrine cell degeneration	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0001406	abnormal gait	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387326	M	MP:0003674	oxidative stress	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0011593	increased catalase activity	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0001393	ataxia	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387326	M	MP:0003674	oxidative stress	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387326	M	MP:0001393	ataxia	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387326	M	MP:0008236	decreased susceptibility to neuronal excitotoxicity	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15703386
MGI:2387326	M	MP:0000886	abnormal cerebellar granule layer morphology	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0004215	abnormal myocardial fiber physiology	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387326	M	MP:0011593	increased catalase activity	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387326	M	MP:0009674	decreased birth weight	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387326	M	MP:0008067	retina ganglion cell degeneration	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0012660	increased superoxide dismutase level	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387326	M	MP:0005140	decreased cardiac muscle contractility	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387326	M	MP:0001405	impaired coordination	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387326	M	MP:0001625	cardiac hypertrophy	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387326	M	MP:0031606	increased susceptibility to age-related retinal degeneration	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0009763	increased susceptibility to induced morbidity/mortality	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387326	M	MP:0000886	abnormal cerebellar granule layer morphology	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387326	M	MP:0002753	dilated heart left ventricle	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387326	M	MP:0000745	tremors	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387326	M	MP:0001265	decreased body size	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387326	M	MP:0001544	abnormal cardiovascular system physiology	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387326	M	MP:0001333	absent optic nerve	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387326	M	MP:0002066	abnormal motor capabilities/coordination/movement	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387326	M	MP:0001732	postnatal growth retardation	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387326	M	MP:0000416	sparse hair	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:2387326	M	MP:0008519	thin retina outer plexiform layer	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0000950	abnormal seizure response to pharmacological agent	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15703386
MGI:2387326	M	MP:0008406	increased cellular sensitivity to hydrogen peroxide	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0003222	increased cardiomyocyte apoptosis	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387326	M	MP:0000343	abnormal response to cardiac infarction	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	15933268
MGI:2387326	M	MP:0004097	abnormal cerebellar cortex morphology	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	12353028
MGI:2387326	M	MP:0002083	premature death	Aifm1<Hq>/Y	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	18791645
MGI:2387448	F	MP:0005366	variegated coat color	Atp7a<Mo-N>/Atp7a<+>	Not Specified	N	MGI:63057
MGI:2387448	F	MP:0001274	curly vibrissae	Atp7a<Mo-N>/Atp7a<+>	Not Specified	N	MGI:63057
MGI:2387449	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-N>/Y	Not Specified	N	MGI:63057
MGI:2387451	F	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-ca>/Atp7a<Mo-ca>	Not Specified	N	11386751
MGI:2387452	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-ca>/Y	Not Specified	N	11386751
MGI:2387453	F	MP:0001274	curly vibrissae	Atp7a<Mo-ca>/Atp7a<+>	Not Specified	N	11386751
MGI:2387463	F	MP:0005366	variegated coat color	Atp7a<Mo-17H>/Atp7a<+>	Not Specified	N	11386751
MGI:2387465	F	MP:0005366	variegated coat color	Atp7a<Mo-16H>/Atp7a<+>	SWF	N	11386751
MGI:2387470	F	MP:0005366	variegated coat color	Atp7a<Mo-spot>/Atp7a<+>	Not Specified	N	11386751
MGI:2387669	F	MP:0005366	variegated coat color	Atp7a<Mo-10H>/Atp7a<+>	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2387670	M	MP:0001274	curly vibrissae	Atp7a<Mo-10H>/Y	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2387670	M	MP:0011085	postnatal lethality, complete penetrance	Atp7a<Mo-10H>/Y	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2387670	M	MP:0001405	impaired coordination	Atp7a<Mo-10H>/Y	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2387670	M	MP:0005171	absent coat pigmentation	Atp7a<Mo-10H>/Y	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2387673	F	MP:0011090	perinatal lethality, incomplete penetrance	Atp7a<Mo-11H>/Atp7a<+>	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2387673	F	MP:0005366	variegated coat color	Atp7a<Mo-11H>/Atp7a<+>	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2387674	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-11H>/Y	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2387674	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-11H>/Y	involves: 101/H * C3H/HeH	N	9147646
MGI:2387677	M	MP:0011100	preweaning lethality, complete penetrance	Atp7a<Mo-12H>/Y	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2387678	F	MP:0002115	abnormal limb bone morphology	Atp7a<Mo-12H>/Atp7a<+>	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2387678	F	MP:0001525	impaired balance	Atp7a<Mo-12H>/Atp7a<+>	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2387678	F	MP:0005366	variegated coat color	Atp7a<Mo-12H>/Atp7a<+>	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2387678	F	MP:0001405	impaired coordination	Atp7a<Mo-12H>/Atp7a<+>	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2387678	F	MP:0001274	curly vibrissae	Atp7a<Mo-12H>/Atp7a<+>	involves: 101/H * C3H/HeH	N	MGI:64387
MGI:2388019	M	MP:0003415	priapism	Usp14<ax-J>/Usp14<ax-J>	involves: STOCK Mafb<kr>	N	5855800
MGI:2388019	F	MP:0001926	female infertility	Usp14<ax-J>/Usp14<ax-J>	involves: STOCK Mafb<kr>	N	MGI:75504
MGI:2388019	M	MP:0001925	male infertility	Usp14<ax-J>/Usp14<ax-J>	involves: STOCK Mafb<kr>	N	MGI:75504
MGI:2388127	M	MP:0005159	azoospermia	crsp/crsp	FVB/N-crsp	N	11353515
MGI:2388127	M	MP:0001155	arrest of spermatogenesis	crsp/crsp	FVB/N-crsp	N	11353515
MGI:2388127	M	MP:0002286	cryptorchism	crsp/crsp	FVB/N-crsp	N	11353515
MGI:2388127	M	MP:0001925	male infertility	crsp/crsp	FVB/N-crsp	N	11353515
MGI:2388127	M	MP:0002669	abnormal scrotum morphology	crsp/crsp	FVB/N-crsp	N	11353515
MGI:2388134	M	MP:0001925	male infertility	Rxfp2<tm1Aia>/Rxfp2<tm1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	12217959
MGI:2388134	M	MP:0001155	arrest of spermatogenesis	Rxfp2<tm1Aia>/Rxfp2<tm1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	12217959
MGI:2388134	M	MP:0031287	bilateral cryptorchism	Rxfp2<tm1Aia>/Rxfp2<tm1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	12217959
MGI:2388134	M	MP:0005159	azoospermia	Rxfp2<tm1Aia>/Rxfp2<tm1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	12217959
MGI:2388134	M	MP:0001147	small testis	Rxfp2<tm1Aia>/Rxfp2<tm1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	12217959
MGI:2388917	M	MP:0001147	small testis	Nppc<lbab>/Nppc<lbab>	either: (involves: C57BL/6J * PL/J) or PL/J	N	MGI:2387428
MGI:2429343	M	MP:0009376	abnormal manchette morphology	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	2346121
MGI:2429343	M	MP:0008545	absent sperm flagellum	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	MGI:62168
MGI:2429343	M	MP:0009232	abnormal sperm nucleus morphology	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	2346121
MGI:2429343	M	MP:0001922	reduced male fertility	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	MGI:62168
MGI:2429343	M	MP:0005578	teratozoospermia	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	MGI:62168
MGI:2429343	M	MP:0006380	abnormal spermatid morphology	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	2346121
MGI:2429343	M	MP:0001155	arrest of spermatogenesis	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	12075009
MGI:2429343	M	MP:0006380	abnormal spermatid morphology	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	1759685
MGI:2429343	M	MP:0006380	abnormal spermatid morphology	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	12075009
MGI:2429343	M	MP:0001156	abnormal spermatogenesis	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	12075009
MGI:2429343	M	MP:0001932	abnormal spermiogenesis	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	2346121
MGI:2429343	M	MP:0009377	ectopic manchette	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	2346121
MGI:2429343	M	MP:0008893	detached sperm flagellum	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	12075009
MGI:2429343	M	MP:0005578	teratozoospermia	Hook1<azh>/Hook1<azh>	involves: C57BL/6J * SWR/J	N	12075009
MGI:2429428	M	MP:0000428	abnormal craniofacial morphology	exma/Y	FVB/N-exma	N	11956759
MGI:2429428	M	MP:0011087	neonatal lethality, complete penetrance	exma/Y	FVB/N-exma	N	11956759
MGI:2429428	M	MP:0001293	anophthalmia	exma/Y	FVB/N-exma	N	11956759
MGI:2429428	M	MP:0001698	decreased embryo size	exma/Y	FVB/N-exma	N	11956759
MGI:2429428	M	MP:0000914	exencephaly	exma/Y	FVB/N-exma	N	11956759
MGI:2429428	M	MP:0000783	abnormal forebrain morphology	exma/Y	FVB/N-exma	N	11956759
MGI:2429431	F	MP:0001297	microphthalmia	exma/exma<+>	FVB/N-exma	N	11956759
MGI:2429431	F	MP:0001293	anophthalmia	exma/exma<+>	FVB/N-exma	N	11956759
MGI:2429431	F	MP:0000914	exencephaly	exma/exma<+>	FVB/N-exma	N	11956759
MGI:2429431	F	MP:0000372	irregular coat pigmentation	exma/exma<+>	FVB/N-exma	N	11956759
MGI:2429431	F	MP:0001394	circling	exma/exma<+>	FVB/N-exma	N	11956759
MGI:2429431	F	MP:0000438	abnormal cranium morphology	exma/exma<+>	FVB/N-exma	N	11956759
MGI:2429434	F	MP:0001386	abnormal maternal nurturing	Ctnna2<cdf>/Ctnna2<cdf>	C3Sn.C3-Ctnna2<cdf>/J	N	9060409
MGI:2429434	M	MP:0001922	reduced male fertility	Ctnna2<cdf>/Ctnna2<cdf>	C3Sn.C3-Ctnna2<cdf>/J	N	9060409
MGI:2429561	M	MP:0008528	polycystic kidney	Nek8<jck>/Nek8<jck>	involves: C57BL/6J	N	12405636
MGI:2429561	M	MP:0003068	enlarged kidney	Nek8<jck>/Nek8<jck>	involves: C57BL/6J	N	12405636
MGI:2429561	F	MP:0001386	abnormal maternal nurturing	Nek8<jck>/Nek8<jck>	involves: C57BL/6J	N	8510385
MGI:2429561	M	MP:0004860	dilated kidney collecting duct	Nek8<jck>/Nek8<jck>	involves: C57BL/6J	N	12405636
MGI:2429561	M	MP:0000522	kidney cortex cyst	Nek8<jck>/Nek8<jck>	involves: C57BL/6J	N	12405636
MGI:2429561	M	MP:0011307	kidney medulla cyst	Nek8<jck>/Nek8<jck>	involves: C57BL/6J	N	12405636
MGI:2429787	M	MP:0001147	small testis	Hmox1<tm1Poss>/Hmox1<tm1Poss>	involves: 129S2/SvPas * C57BL/6	N	9380735
MGI:2446583	F	MP:0001921	reduced fertility	Abcd1<tm1Kan>/Abcd1<tm1Kan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9418970
MGI:2446583	F	MP:0002118	abnormal lipid homeostasis	Abcd1<tm1Kan>/Abcd1<tm1Kan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9418970
MGI:2446586	M	MP:0002118	abnormal lipid homeostasis	Abcd1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9418970
MGI:2446586	M	MP:0001921	reduced fertility	Abcd1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9418970
MGI:2446588	F	MP:0002118	abnormal lipid homeostasis	Abcd1<tm1Kds>/Abcd1<tm1Kds>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	N	9256488
MGI:2446588	F	MP:0005284	increased saturated fatty acids level	Abcd1<tm1Kds>/Abcd1<tm1Kds>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	N	9256488
MGI:2446589	M	MP:0002118	abnormal lipid homeostasis	Abcd1<tm1Kds>/Y	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	N	9256488
MGI:2446589	M	MP:0005284	increased saturated fatty acids level	Abcd1<tm1Kds>/Y	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	N	9256488
MGI:2446591	F	MP:0002118	abnormal lipid homeostasis	Abcd1<tm1Ymd>/Abcd1<tm1Ymd>	involves: 129S/SvEv * C57BL/6J * DBA/2J	N	9126326
MGI:2446595	M	MP:0002118	abnormal lipid homeostasis	Abcd1<tm1Ymd>/Y	involves: 129S/SvEv * C57BL/6J * DBA/2J	N	9126326
MGI:2447583	F	MP:0001931	abnormal oogenesis	Dnmt3l<tm1Enl>/Dnmt3l<tm1Enl>	involves: 129S4/SvJae	N	11934864
MGI:2447583	M	MP:0001932	abnormal spermiogenesis	Dnmt3l<tm1Enl>/Dnmt3l<tm1Enl>	involves: 129S4/SvJae	N	11934864
MGI:2447583	M	MP:0001147	small testis	Dnmt3l<tm1Enl>/Dnmt3l<tm1Enl>	involves: 129S4/SvJae	N	11934864
MGI:2447608	F	MP:0001923	reduced female fertility	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * ICR)	N	12409213
MGI:2447785	F	MP:0001882	abnormal lactation	Tsg101<tm1Kuw>/Tsg101<tm1Kuw>,Tg(Wap-cre)11738Mam/0	Not Specified	N	12482969
MGI:2447785	F	MP:0006270	abnormal mammary gland growth during lactation	Tsg101<tm1Kuw>/Tsg101<tm1Kuw>,Tg(Wap-cre)11738Mam/0	Not Specified	N	12482969
MGI:2447785	F	MP:0000628	abnormal mammary gland development	Tsg101<tm1Kuw>/Tsg101<tm1Kuw>,Tg(Wap-cre)11738Mam/0	Not Specified	N	12482969
MGI:2447790	F	MP:0009006	prolonged estrous cycle	Adcyap1r1<tm1Bbt>/Adcyap1r1<tm1Bbt>	involves: 129 * C57BL/6J	N	11193864
MGI:2447790	F	MP:0009011	prolonged diestrus	Adcyap1r1<tm1Bbt>/Adcyap1r1<tm1Bbt>	involves: 129 * C57BL/6J	N	11193864
MGI:2447790	F	MP:0001923	reduced female fertility	Adcyap1r1<tm1Bbt>/Adcyap1r1<tm1Bbt>	involves: 129 * C57BL/6J	N	11193864
MGI:2448278	F	MP:0001360	abnormal social investigation	tmgc10/tmgc10	involves: D7R75M	N	17629744
MGI:2448896	F	MP:0003732	abnormal retina outer plexiform layer morphology	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	16088326
MGI:2448896	F	MP:0006069	abnormal retina neuronal layer morphology	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	16088326
MGI:2448896	F	MP:0005240	abnormal amacrine cell morphology	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	MGI:2448159
MGI:2448896	F	MP:0001004	abnormal retina photoreceptor morphology	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	MGI:2448159
MGI:2448896	F	MP:0005551	abnormal eye electrophysiology	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	16088326
MGI:2448896	F	MP:0005551	abnormal eye electrophysiology	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	MGI:2448159
MGI:2448896	F	MP:0005201	abnormal retina pigment epithelium morphology	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	MGI:2448159
MGI:2448896	F	MP:0001328	disorganized retina layers	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	16088326
MGI:2448896	F	MP:0003733	abnormal retina inner nuclear layer morphology	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	16088326
MGI:2448896	F	MP:0003729	abnormal photoreceptor outer segment morphology	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	16088326
MGI:2448896	F	MP:0003730	abnormal photoreceptor inner segment morphology	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	16088326
MGI:2448896	F	MP:0002864	abnormal ocular fundus morphology	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	16088326
MGI:2448896	F	MP:0003731	abnormal retina outer nuclear layer morphology	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	16088326
MGI:2448896	F	MP:0003728	abnormal retina photoreceptor layer morphology	Rs1<tmgc1>/Rs1<tmgc1>	involves: C3H/Rl * C57BL/6	N	16088326
MGI:2449114	M	MP:0001762	polyuria	Aprt<tm1Jat>/Aprt<tm1Jat>	involves: 129S2/SvPas * Black Swiss	N	9689017
MGI:2449114	M	MP:0005558	decreased creatinine clearance	Aprt<tm1Jat>/Aprt<tm1Jat>	involves: 129S2/SvPas * Black Swiss	N	9689017
MGI:2449114	M	MP:0011941	increased fluid intake	Aprt<tm1Jat>/Aprt<tm1Jat>	involves: 129S2/SvPas * Black Swiss	N	9689017
MGI:2449114	M	MP:0000208	decreased hematocrit	Aprt<tm1Jat>/Aprt<tm1Jat>	involves: 129S2/SvPas * Black Swiss	N	9689017
MGI:2449114	M	MP:0003918	decreased kidney weight	Aprt<tm1Jat>/Aprt<tm1Jat>	involves: 129S2/SvPas * Black Swiss	N	9689017
MGI:2449115	M	MP:0011844	kidney collecting duct atrophy	Aprt<tm1Jat>/Aprt<tm1Jat>	involves: 129S2/SvPas * C57BL/6J	N	11532086
MGI:2449164	M	MP:0001922	reduced male fertility	Myo7a<sh1>/Myo7a<sh1>	involves: BALB	N	MGI:63673
MGI:2449173	M	MP:0001925	male infertility	Myo7a<sh1-6J>/Myo7a<sh1-6J>	involves: C57BLKS/J	N	MGI:65387
MGI:2449447	F	MP:0001119	abnormal female reproductive system morphology	Rara<tm1Ipc>/Rara<tm1Ipc>,Rarb<tm1Ipc>/Rarb<tm1Ipc>	involves: 129S2/SvPas	N	7607068
MGI:2449447	F	MP:0003558	absent uterus	Rara<tm1Ipc>/Rara<tm1Ipc>,Rarb<tm1Ipc>/Rarb<tm1Ipc>	involves: 129S2/SvPas	N	7607068
MGI:2449447	F	MP:0003575	absent oviduct	Rara<tm1Ipc>/Rara<tm1Ipc>,Rarb<tm1Ipc>/Rarb<tm1Ipc>	involves: 129S2/SvPas	N	7607068
MGI:2449447	F	MP:0009072	absent cranial vagina	Rara<tm1Ipc>/Rara<tm1Ipc>,Rarb<tm1Ipc>/Rarb<tm1Ipc>	involves: 129S2/SvPas	N	7607068
MGI:2449454	F	MP:0008498	decreased IgG3 level	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0002460	decreased immunoglobulin level	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0005466	abnormal T-helper 2 physiology	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0002420	abnormal adaptive immunity	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0002492	decreased IgE level	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0000685	abnormal immune system morphology	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0008495	decreased IgG1 level	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0002491	decreased IgD level	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0008074	increased CD4-positive, alpha-beta T cell number	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0008396	abnormal osteoclast differentiation	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	17360404
MGI:2449454	F	MP:0002145	abnormal T cell differentiation	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0005092	decreased double-positive T cell number	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0008474	absent spleen germinal center	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0001790	abnormal immune system physiology	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0004816	abnormal class switch recombination	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449454	F	MP:0001807	decreased IgA level	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	involves: 129S2/SvPas * C57BL/6	N	7882172
MGI:2449488	M	MP:0014469	abnormal B cell calcium ion homeostasis	Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15331445
MGI:2449488	M	MP:0002144	abnormal B cell differentiation	Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8890160
MGI:2449488	M	MP:0008215	decreased immature B cell number	Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8890160
MGI:2449488	M	MP:0001806	decreased IgM level	Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8890160
MGI:2449488	M	MP:0008203	absent B-1a cells	Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8890160
MGI:2449488	M	MP:0001800	abnormal humoral immune response	Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * C57BL/6	N	14634110
MGI:2449488	M	MP:0001790	abnormal immune system physiology	Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8890160
MGI:2449488	M	MP:0002460	decreased immunoglobulin level	Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * C57BL/6	N	14634110
MGI:2449488	M	MP:0005017	decreased B cell number	Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8890160
MGI:2449488	M	MP:0008498	decreased IgG3 level	Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8890160
MGI:2449488	M	MP:0008212	absent mature B cells	Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8890160
MGI:2449491	M	MP:0001807	decreased IgA level	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	N	7964465
MGI:2449491	M	MP:0002722	abnormal immune system organ morphology	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	N	7964465
MGI:2449491	M	MP:0008101	lymph node hypoplasia	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	N	7964465
MGI:2449491	M	MP:0005387	immune system phenotype	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	Y	7964465
MGI:2449491	M	MP:0008523	absent lymph node germinal center	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	N	7964465
MGI:2449491	M	MP:0008474	absent spleen germinal center	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	N	7964465
MGI:2449491	M	MP:0001835	abnormal antigen presentation	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	N	7964465
MGI:2449491	M	MP:0004816	abnormal class switch recombination	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	N	7964465
MGI:2449491	M	MP:0002460	decreased immunoglobulin level	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	N	7964465
MGI:2449491	M	MP:0008497	decreased IgG2b level	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	N	7964465
MGI:2449491	M	MP:0008495	decreased IgG1 level	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	N	7964465
MGI:2449491	M	MP:0002492	decreased IgE level	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	N	7964465
MGI:2449491	M	MP:0001790	abnormal immune system physiology	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	N	7964465
MGI:2449491	M	MP:0002339	abnormal lymph node morphology	Cd40lg<tm1Imx>/Y	involves: 129S2/SvPas * C57BL/6	N	7964465
MGI:2449543	F	MP:0002551	abnormal blood coagulation	F8<tm1Kaz>/F8<tm1Kaz>	involves: 129S4/SvJae * C57BL/6	N	8896409
MGI:2449543	F	MP:0005397	hematopoietic system phenotype	F8<tm1Kaz>/F8<tm1Kaz>	involves: 129S4/SvJae * C57BL/6	Y	8896409
MGI:2449543	F	MP:0005389	reproductive system phenotype	F8<tm1Kaz>/F8<tm1Kaz>	involves: 129S4/SvJae * C57BL/6	Y	8896409
MGI:2449543	F	MP:0009763	increased susceptibility to induced morbidity/mortality	F8<tm1Kaz>/F8<tm1Kaz>	involves: 129S4/SvJae * C57BL/6	N	8896409
MGI:2449544	M	MP:0005397	hematopoietic system phenotype	F8<tm1Kaz>/Y	involves: 129S4/SvJae * C57BL/6	Y	8896409
MGI:2449544	M	MP:0005397	hematopoietic system phenotype	F8<tm1Kaz>/Y	involves: 129S4/SvJae * C57BL/6	Y	7647782
MGI:2449544	M	MP:0005000	abnormal immune tolerance	F8<tm1Kaz>/Y	involves: 129S4/SvJae * C57BL/6	N	16493498
MGI:2449544	M	MP:0002551	abnormal blood coagulation	F8<tm1Kaz>/Y	involves: 129S4/SvJae * C57BL/6	N	8896409
MGI:2449544	M	MP:0009763	increased susceptibility to induced morbidity/mortality	F8<tm1Kaz>/Y	involves: 129S4/SvJae * C57BL/6	N	8896409
MGI:2449544	M	MP:0009763	increased susceptibility to induced morbidity/mortality	F8<tm1Kaz>/Y	involves: 129S4/SvJae * C57BL/6	N	7647782
MGI:2449544	M	MP:0002551	abnormal blood coagulation	F8<tm1Kaz>/Y	involves: 129S4/SvJae * C57BL/6	N	7647782
MGI:2449546	M	MP:0002551	abnormal blood coagulation	F8<tm2Kaz>/Y	involves: 129S4/SvJae * C57BL/6	N	7647782
MGI:2449546	M	MP:0002551	abnormal blood coagulation	F8<tm2Kaz>/Y	involves: 129S4/SvJae * C57BL/6	N	8896409
MGI:2449556	M	MP:0002451	abnormal macrophage physiology	Cybb<tm1Din>/Y	involves: 129S/SvEv * C57BL/6	N	7719350
MGI:2449556	M	MP:0001625	cardiac hypertrophy	Cybb<tm1Din>/Y	involves: 129S/SvEv * C57BL/6	N	14551238
MGI:2449556	M	MP:0002843	decreased systemic arterial blood pressure	Cybb<tm1Din>/Y	involves: 129S/SvEv * C57BL/6	N	11349005
MGI:2449556	M	MP:0002463	abnormal neutrophil physiology	Cybb<tm1Din>/Y	involves: 129S/SvEv * C57BL/6	N	7719350
MGI:2449556	M	MP:0006264	decreased systemic arterial systolic blood pressure	Cybb<tm1Din>/Y	involves: 129S/SvEv * C57BL/6	N	14551238
MGI:2449556	M	MP:0002406	increased susceptibility to infection	Cybb<tm1Din>/Y	involves: 129S/SvEv * C57BL/6	N	7719350
MGI:2449556	M	MP:0001846	increased inflammatory response	Cybb<tm1Din>/Y	involves: 129S/SvEv * C57BL/6	N	7719350
MGI:2449556	M	MP:0001790	abnormal immune system physiology	Cybb<tm1Din>/Y	involves: 129S/SvEv * C57BL/6	N	7719350
MGI:2449556	M	MP:0002412	increased susceptibility to bacterial infection	Cybb<tm1Din>/Y	involves: 129S/SvEv * C57BL/6	N	7719350
MGI:2449556	M	MP:0009873	abnormal aorta tunica media morphology	Cybb<tm1Din>/Y	involves: 129S/SvEv * C57BL/6	N	11349005
MGI:2449556	M	MP:0001262	decreased body weight	Cybb<tm1Din>/Y	involves: 129S/SvEv * C57BL/6	N	11349005
MGI:2449968	F	MP:0010249	lactation failure	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449968	F	MP:0001134	absent corpus luteum	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449968	F	MP:0031239	increased atretic ovarian follicle number	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449968	F	MP:0004905	decreased uterus weight	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449968	F	MP:0001923	reduced female fertility	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449968	F	MP:0004856	decreased ovary weight	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449968	F	MP:0009006	prolonged estrous cycle	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449968	F	MP:0001132	absent mature ovarian follicles	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449968	M	MP:0004910	decreased seminal vesicle weight	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449968	F	MP:0009066	decreased oviduct weight	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449968	M	MP:0001922	reduced male fertility	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449968	F	MP:0009009	absent estrous cycle	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449968	M	MP:0004852	decreased testis weight	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449968	F	MP:0001131	abnormal ovarian follicle morphology	Vgf<tm1Srjs>/Vgf<tm1Srjs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10433265
MGI:2449974	M	MP:0001925	male infertility	Sp4<tm1Sus>/Sp4<tm1Sus>	involves: 129P2/OlaHsd * C57BL/6	N	11532028
MGI:2449974	M	MP:0001147	small testis	Sp4<tm1Sus>/Sp4<tm1Sus>	involves: 129P2/OlaHsd * C57BL/6	N	11532028
MGI:2449974	F	MP:0002637	small uterus	Sp4<tm1Sus>/Sp4<tm1Sus>	involves: 129P2/OlaHsd * C57BL/6	N	11532028
MGI:2449974	F	MP:0001923	reduced female fertility	Sp4<tm1Sus>/Sp4<tm1Sus>	involves: 129P2/OlaHsd * C57BL/6	N	11532028
MGI:2449977	M	MP:0002216	abnormal seminiferous tubule morphology	Sbf1<tm1Mlc>/Sbf1<tm1Mlc>	involves: C57BL/6	N	11994405
MGI:2449977	M	MP:0001925	male infertility	Sbf1<tm1Mlc>/Sbf1<tm1Mlc>	involves: C57BL/6	N	11994405
MGI:2449977	M	MP:0006380	abnormal spermatid morphology	Sbf1<tm1Mlc>/Sbf1<tm1Mlc>	involves: C57BL/6	N	11994405
MGI:2449977	M	MP:0001147	small testis	Sbf1<tm1Mlc>/Sbf1<tm1Mlc>	involves: C57BL/6	N	11994405
MGI:2449977	M	MP:0005159	azoospermia	Sbf1<tm1Mlc>/Sbf1<tm1Mlc>	involves: C57BL/6	N	11994405
MGI:2449977	M	MP:0001156	abnormal spermatogenesis	Sbf1<tm1Mlc>/Sbf1<tm1Mlc>	involves: C57BL/6	N	11994405
MGI:2449982	M	MP:0001167	prostate gland epithelial hyperplasia	Rxra<tm1Krc>/Rxra<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	12183441
MGI:2449982	M	MP:0009736	abnormal prostate gland branching morphogenesis	Rxra<tm1Krc>/Rxra<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	12183441
MGI:2449982	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Rxra<tm1Krc>/Rxra<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	12183441
MGI:2449983	M	MP:0003607	abnormal prostate gland physiology	Rxra<tm1Krc>/Rxra<tm1Krc>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	12183441
MGI:2449983	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Rxra<tm1Krc>/Rxra<tm1Krc>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	12183441
MGI:2449983	M	MP:0009736	abnormal prostate gland branching morphogenesis	Rxra<tm1Krc>/Rxra<tm1Krc>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	12183441
MGI:2450069	M	MP:0001155	arrest of spermatogenesis	Hspa2<tm1Dix>/Hspa2<tm1Dix>	either: 129S/SvEv or C57BL/6	N	8622925
MGI:2450069	M	MP:0005169	abnormal male meiosis	Hspa2<tm1Dix>/Hspa2<tm1Dix>	either: 129S/SvEv or C57BL/6	N	8622925
MGI:2450069	M	MP:0004852	decreased testis weight	Hspa2<tm1Dix>/Hspa2<tm1Dix>	either: 129S/SvEv or C57BL/6	N	8622925
MGI:2450069	M	MP:0001925	male infertility	Hspa2<tm1Dix>/Hspa2<tm1Dix>	either: 129S/SvEv or C57BL/6	N	8622925
MGI:2450121	M	MP:0008261	arrest of male meiosis	Gal3st1<tm1Kho>/Gal3st1<tm1Kho>	involves: 129P2/OlaHsd	N	11917099
MGI:2450121	M	MP:0004852	decreased testis weight	Gal3st1<tm1Kho>/Gal3st1<tm1Kho>	involves: 129P2/OlaHsd	N	11917099
MGI:2450121	M	MP:0020550	multinucleated giant male germ cells	Gal3st1<tm1Kho>/Gal3st1<tm1Kho>	involves: 129P2/OlaHsd	N	11917099
MGI:2450121	M	MP:0005159	azoospermia	Gal3st1<tm1Kho>/Gal3st1<tm1Kho>	involves: 129P2/OlaHsd	N	11917099
MGI:2450121	M	MP:0014052	increased male germ cell apoptosis	Gal3st1<tm1Kho>/Gal3st1<tm1Kho>	involves: 129P2/OlaHsd	N	11917099
MGI:2450121	M	MP:0001146	abnormal testis morphology	Gal3st1<tm1Kho>/Gal3st1<tm1Kho>	involves: 129P2/OlaHsd	N	11917099
MGI:2450121	M	MP:0001925	male infertility	Gal3st1<tm1Kho>/Gal3st1<tm1Kho>	involves: 129P2/OlaHsd	N	11917099
MGI:2450121	M	MP:0001155	arrest of spermatogenesis	Gal3st1<tm1Kho>/Gal3st1<tm1Kho>	involves: 129P2/OlaHsd	N	11917099
MGI:2450122	M	MP:0020355	abnormal Sertoli cell barrier morphology	Cldn11<tm1Ral>/Cldn11<tm1Ral>	Not Specified	N	10612400
MGI:2450122	M	MP:0001925	male infertility	Cldn11<tm1Ral>/Cldn11<tm1Ral>	Not Specified	N	10612400
MGI:2450122	M	MP:0002216	abnormal seminiferous tubule morphology	Cldn11<tm1Ral>/Cldn11<tm1Ral>	Not Specified	N	10612400
MGI:2450122	M	MP:0005159	azoospermia	Cldn11<tm1Ral>/Cldn11<tm1Ral>	Not Specified	N	10612400
MGI:2450122	M	MP:0001156	abnormal spermatogenesis	Cldn11<tm1Ral>/Cldn11<tm1Ral>	Not Specified	N	10612400
MGI:2450122	M	MP:0001147	small testis	Cldn11<tm1Ral>/Cldn11<tm1Ral>	Not Specified	N	10612400
MGI:2450128	M	MP:0004961	increased prostate gland weight	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	9618522
MGI:2450128	M	MP:0001932	abnormal spermiogenesis	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	M	MP:0003509	increased circulating dihydrotestosterone level	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	11356695
MGI:2450128	F	MP:0005319	abnormal enzyme/coenzyme level	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	15178650
MGI:2450128	M	MP:0002631	abnormal epididymis morphology	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	F	MP:0004905	decreased uterus weight	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10875266
MGI:2450128	F	MP:0003572	abnormal uterus development	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10875266
MGI:2450128	M	MP:0006362	abnormal male germ cell morphology	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	M	MP:0001925	male infertility	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	M	MP:0001156	abnormal spermatogenesis	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	F	MP:0003511	abnormal labium morphology	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	9618522
MGI:2450128	M	MP:0031354	abnormal acrosome assembly	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	M	MP:0002781	increased circulating testosterone level	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	F	MP:0001121	uterus hypoplasia	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	9618522
MGI:2450128	M	MP:0020550	multinucleated giant male germ cells	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	F	MP:0001926	female infertility	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	9618522
MGI:2450128	F	MP:0001926	female infertility	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10875266
MGI:2450128	M	MP:0005305	prostate gland anterior lobe hyperplasia	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	11356695
MGI:2450128	M	MP:0004909	increased seminal vesicle weight	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	9618522
MGI:2450128	M	MP:0005124	increased circulating prolactin level	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	11356695
MGI:2450128	M	MP:0004852	decreased testis weight	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	F	MP:0001129	impaired ovarian folliculogenesis	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10875266
MGI:2450128	M	MP:0001152	increased Leydig cell number	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	F	MP:0009444	ovarian follicular cyst	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10875266
MGI:2450128	F	MP:0004876	decreased mean systemic arterial blood pressure	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	15178650
MGI:2450128	F	MP:0001129	impaired ovarian folliculogenesis	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	9618522
MGI:2450128	M	MP:0004961	increased prostate gland weight	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	11356695
MGI:2450128	F	MP:0003929	decreased heart rate variability	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	15178650
MGI:2450128	M	MP:0006380	abnormal spermatid morphology	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	F	MP:0002626	increased heart rate	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	15178650
MGI:2450128	F	MP:0005599	increased cardiac muscle contractility	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	15178650
MGI:2450128	M	MP:0031364	increased prostate gland ventral lobe weight	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	11356695
MGI:2450128	F	MP:0001126	abnormal ovary morphology	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	9618522
MGI:2450128	M	MP:0004901	decreased male germ cell number	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	F	MP:0001134	absent corpus luteum	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	9618522
MGI:2450128	M	MP:0001750	increased circulating follicle stimulating hormone level	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	M	MP:0000659	prostate gland hyperplasia	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	11356695
MGI:2450128	F	MP:0001134	absent corpus luteum	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10875266
MGI:2450128	M	MP:0031365	prostate gland ventral lobe hyperplasia	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	11356695
MGI:2450128	F	MP:0013508	increased granulosa cell apoptosis	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10875266
MGI:2450128	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	M	MP:0002781	increased circulating testosterone level	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	11356695
MGI:2450128	F	MP:0003529	enlarged clitoris	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	9618522
MGI:2450128	M	MP:0003607	abnormal prostate gland physiology	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	11356695
MGI:2450128	M	MP:0001145	abnormal male reproductive system morphology	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	9618522
MGI:2450128	F	MP:0008869	anovulation	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10875266
MGI:2450128	M	MP:0008279	arrest of spermiogenesis	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	F	MP:0000230	abnormal systemic arterial blood pressure	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	15178650
MGI:2450128	M	MP:0031361	increased prostate gland anterior lobe weight	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	11356695
MGI:2450128	F	MP:0006263	decreased systemic arterial diastolic blood pressure	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	15178650
MGI:2450128	F	MP:0004834	ovary hemorrhage	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10875266
MGI:2450128	M	MP:0002216	abnormal seminiferous tubule morphology	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	M	MP:0031369	prostate gland dorsolateral lobe hyperplasia	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	11356695
MGI:2450128	M	MP:0031368	increased prostate gland dorsolateral lobe weight	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	11356695
MGI:2450128	M	MP:0004958	enlarged prostate gland	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	11356695
MGI:2450128	F	MP:0001126	abnormal ovary morphology	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10875266
MGI:2450128	M	MP:0001751	increased circulating luteinizing hormone level	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450128	M	MP:0014052	increased male germ cell apoptosis	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac * C57BL/6	N	10393934
MGI:2450130	M	MP:0001925	male infertility	Fancc<tm1Mab>/Fancc<tm1Mab>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	8630504
MGI:2450130	M	MP:0001154	seminiferous tubule degeneration	Fancc<tm1Mab>/Fancc<tm1Mab>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	8630504
MGI:2450130	M	MP:0003205	testicular atrophy	Fancc<tm1Mab>/Fancc<tm1Mab>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	8630504
MGI:2450130	M	MP:0001155	arrest of spermatogenesis	Fancc<tm1Mab>/Fancc<tm1Mab>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	8630504
MGI:2450130	F	MP:0001126	abnormal ovary morphology	Fancc<tm1Mab>/Fancc<tm1Mab>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	8630504
MGI:2450130	F	MP:0001129	impaired ovarian folliculogenesis	Fancc<tm1Mab>/Fancc<tm1Mab>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	8630504
MGI:2450130	F	MP:0001134	absent corpus luteum	Fancc<tm1Mab>/Fancc<tm1Mab>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	8630504
MGI:2450130	F	MP:0001926	female infertility	Fancc<tm1Mab>/Fancc<tm1Mab>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	8630504
MGI:2450131	M	MP:0002675	asthenozoospermia	Catsper1<tm1Clph>/Catsper1<tm1Clph>	involves: 129S4/SvJae * C57BL/6J	N	11595941
MGI:2450131	M	MP:0004543	abnormal sperm physiology	Catsper1<tm1Clph>/Catsper1<tm1Clph>	involves: 129S4/SvJae * C57BL/6J	N	11595941
MGI:2450131	M	MP:0030976	impaired sperm penetration of zona pellucida	Catsper1<tm1Clph>/Catsper1<tm1Clph>	involves: 129S4/SvJae * C57BL/6J	N	11595941
MGI:2450131	M	MP:0001925	male infertility	Catsper1<tm1Clph>/Catsper1<tm1Clph>	involves: 129S4/SvJae * C57BL/6J	N	11595941
MGI:2450132	M	MP:0002216	abnormal seminiferous tubule morphology	Fancc<tm1Mgo>/Fancc<tm1Mgo>	involves: 129S4/SvJaeSor * C57BL/6	N	8704201
MGI:2450132	F	MP:0005158	ovary hypoplasia	Fancc<tm1Mgo>/Fancc<tm1Mgo>	involves: 129S4/SvJaeSor * C57BL/6	N	8704201
MGI:2450132	F	MP:0001923	reduced female fertility	Fancc<tm1Mgo>/Fancc<tm1Mgo>	involves: 129S4/SvJaeSor * C57BL/6	N	8704201
MGI:2450132	F	MP:0002777	absent ovarian follicles	Fancc<tm1Mgo>/Fancc<tm1Mgo>	involves: 129S4/SvJaeSor * C57BL/6	N	8704201
MGI:2450132	F	MP:0001127	small ovary	Fancc<tm1Mgo>/Fancc<tm1Mgo>	involves: 129S4/SvJaeSor * C57BL/6	N	8704201
MGI:2450132	F	MP:0005431	decreased oocyte number	Fancc<tm1Mgo>/Fancc<tm1Mgo>	involves: 129S4/SvJaeSor * C57BL/6	N	8704201
MGI:2450132	M	MP:0002687	oligozoospermia	Fancc<tm1Mgo>/Fancc<tm1Mgo>	involves: 129S4/SvJaeSor * C57BL/6	N	8704201
MGI:2450132	F	MP:0001121	uterus hypoplasia	Fancc<tm1Mgo>/Fancc<tm1Mgo>	involves: 129S4/SvJaeSor * C57BL/6	N	8704201
MGI:2450132	M	MP:0004852	decreased testis weight	Fancc<tm1Mgo>/Fancc<tm1Mgo>	involves: 129S4/SvJaeSor * C57BL/6	N	8704201
MGI:2450138	F	MP:0001126	abnormal ovary morphology	Afp<tm2Ibmm>/Afp<tm2Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450138	F	MP:0002566	abnormal sexual interaction	Afp<tm2Ibmm>/Afp<tm2Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450138	F	MP:0008869	anovulation	Afp<tm2Ibmm>/Afp<tm2Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450138	F	MP:0009009	absent estrous cycle	Afp<tm2Ibmm>/Afp<tm2Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450138	F	MP:0001926	female infertility	Afp<tm2Ibmm>/Afp<tm2Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450138	F	MP:0001134	absent corpus luteum	Afp<tm2Ibmm>/Afp<tm2Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450138	F	MP:0009092	endometrium hyperplasia	Afp<tm2Ibmm>/Afp<tm2Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450139	F	MP:0002566	abnormal sexual interaction	Afp<tm1Ibmm>/Afp<tm1Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450139	F	MP:0008869	anovulation	Afp<tm1Ibmm>/Afp<tm1Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450139	F	MP:0009092	endometrium hyperplasia	Afp<tm1Ibmm>/Afp<tm1Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450139	F	MP:0009009	absent estrous cycle	Afp<tm1Ibmm>/Afp<tm1Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450139	F	MP:0001126	abnormal ovary morphology	Afp<tm1Ibmm>/Afp<tm1Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450139	F	MP:0001134	absent corpus luteum	Afp<tm1Ibmm>/Afp<tm1Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450139	F	MP:0001926	female infertility	Afp<tm1Ibmm>/Afp<tm1Ibmm>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)	N	12297623
MGI:2450394	M	MP:0001155	arrest of spermatogenesis	Amh<tm1Bhr>/Amh<tm1Bhr>,Ar<Tfm>/Y	either: (involves: 129P3/J * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7954809
MGI:2450394	M	MP:0004727	absent epididymis	Amh<tm1Bhr>/Amh<tm1Bhr>,Ar<Tfm>/Y	either: (involves: 129P3/J * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7954809
MGI:2450394	M	MP:0003557	absent vas deferens	Amh<tm1Bhr>/Amh<tm1Bhr>,Ar<Tfm>/Y	either: (involves: 129P3/J * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7954809
MGI:2450394	M	MP:0001145	abnormal male reproductive system morphology	Amh<tm1Bhr>/Amh<tm1Bhr>,Ar<Tfm>/Y	either: (involves: 129P3/J * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7954809
MGI:2450394	M	MP:0002286	cryptorchism	Amh<tm1Bhr>/Amh<tm1Bhr>,Ar<Tfm>/Y	either: (involves: 129P3/J * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7954809
MGI:2450405	F	MP:0004855	increased ovary weight	Amh<tm1Bhr>/Amh<+>	involves: 129S7/SvEvBrd * C57BL/6	N	10579345
MGI:2450407	M	MP:0001156	abnormal spermatogenesis	Ctsl<fs>/Ctsl<fs>	involves: C57BL/6 * FSB/GnEi	N	12533435
MGI:2450407	M	MP:0004852	decreased testis weight	Ctsl<fs>/Ctsl<fs>	involves: C57BL/6 * FSB/GnEi	N	12533435
MGI:2450407	M	MP:0002216	abnormal seminiferous tubule morphology	Ctsl<fs>/Ctsl<fs>	involves: C57BL/6 * FSB/GnEi	N	12533435
MGI:2450431	M	MP:0001146	abnormal testis morphology	Rad50<tm2Jpt>/Rad50<tm2Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	12208847
MGI:2450432	F	MP:0001119	abnormal female reproductive system morphology	Acsl4<tm1Tty>/Acsl4<+>	involves: C57BL/6NCrj * CBA/JNCrj	N	11409893
MGI:2450432	F	MP:0009671	abnormal uterus physiology	Acsl4<tm1Tty>/Acsl4<+>	involves: C57BL/6NCrj * CBA/JNCrj	N	11409893
MGI:2450432	F	MP:0005376	homeostasis/metabolism phenotype	Acsl4<tm1Tty>/Acsl4<+>	involves: C57BL/6NCrj * CBA/JNCrj	Y	11409893
MGI:2450432	F	MP:0009814	increased prostaglandin level	Acsl4<tm1Tty>/Acsl4<+>	involves: C57BL/6NCrj * CBA/JNCrj	N	11409893
MGI:2450432	F	MP:0002681	increased corpora lutea number	Acsl4<tm1Tty>/Acsl4<+>	involves: C57BL/6NCrj * CBA/JNCrj	N	11409893
MGI:2450432	F	MP:0004832	enlarged ovary	Acsl4<tm1Tty>/Acsl4<+>	involves: C57BL/6NCrj * CBA/JNCrj	N	11409893
MGI:2450432	F	MP:0001923	reduced female fertility	Acsl4<tm1Tty>/Acsl4<+>	involves: C57BL/6NCrj * CBA/JNCrj	N	11409893
MGI:2450432	F	MP:0001935	decreased litter size	Acsl4<tm1Tty>/Acsl4<+>	involves: C57BL/6NCrj * CBA/JNCrj	N	11409893
MGI:2450432	F	MP:0004896	abnormal endometrium morphology	Acsl4<tm1Tty>/Acsl4<+>	involves: C57BL/6NCrj * CBA/JNCrj	N	11409893
MGI:2450432	F	MP:0001123	dilated uterus	Acsl4<tm1Tty>/Acsl4<+>	involves: C57BL/6NCrj * CBA/JNCrj	N	11409893
MGI:2450432	F	MP:0009082	uterus cyst	Acsl4<tm1Tty>/Acsl4<+>	involves: C57BL/6NCrj * CBA/JNCrj	N	11409893
MGI:2450433	M	MP:0002169	no abnormal phenotype detected	Acsl4<tm1Tty>/Y	involves: C57BL/6NCrj * CBA/JNCrj	N	11409893
MGI:2450509	F	MP:0001923	reduced female fertility	Adamts1<tm1Hku>/Adamts1<tm1Hku>	involves: 129S6/SvEvTac * C57BL/6	N	10811842
MGI:2450509	F	MP:0001729	impaired embryo implantation	Adamts1<tm1Hku>/Adamts1<tm1Hku>	involves: 129S6/SvEvTac * C57BL/6	N	10811842
MGI:2450509	F	MP:0001123	dilated uterus	Adamts1<tm1Hku>/Adamts1<tm1Hku>	involves: 129S6/SvEvTac * C57BL/6	N	10811842
MGI:2450509	F	MP:0002682	decreased mature ovarian follicle number	Adamts1<tm1Hku>/Adamts1<tm1Hku>	involves: 129S6/SvEvTac * C57BL/6	N	10811842
MGI:2450509	F	MP:0009082	uterus cyst	Adamts1<tm1Hku>/Adamts1<tm1Hku>	involves: 129S6/SvEvTac * C57BL/6	N	10811842
MGI:2450528	M	MP:0001156	abnormal spermatogenesis	Adamts2<tm1Prc>/Adamts2<tm1Prc>	involves: 129	N	11284712
MGI:2450528	M	MP:0001925	male infertility	Adamts2<tm1Prc>/Adamts2<tm1Prc>	involves: 129	N	11284712
MGI:2450528	M	MP:0002687	oligozoospermia	Adamts2<tm1Prc>/Adamts2<tm1Prc>	involves: 129	N	11284712
MGI:2450541	M	MP:0001147	small testis	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	either: 129 or (involves: 129S7/SvEvBrd * C57BL/6)	N	7885474
MGI:2450541	F	MP:0001126	abnormal ovary morphology	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	either: 129 or (involves: 129S7/SvEvBrd * C57BL/6)	N	7885474
MGI:2450541	M	MP:0005159	azoospermia	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	either: 129 or (involves: 129S7/SvEvBrd * C57BL/6)	N	7885474
MGI:2450541	F	MP:0001926	female infertility	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	either: 129 or (involves: 129S7/SvEvBrd * C57BL/6)	N	7885474
MGI:2450541	F	MP:0031239	increased atretic ovarian follicle number	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	either: 129 or (involves: 129S7/SvEvBrd * C57BL/6)	N	7885474
MGI:2450541	F	MP:0009081	thin uterus	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	either: 129 or (involves: 129S7/SvEvBrd * C57BL/6)	N	7885474
MGI:2450541	M	MP:0002216	abnormal seminiferous tubule morphology	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	either: 129 or (involves: 129S7/SvEvBrd * C57BL/6)	N	7885474
MGI:2450541	F	MP:0001927	abnormal estrous cycle	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	either: 129 or (involves: 129S7/SvEvBrd * C57BL/6)	N	7885474
MGI:2450541	F	MP:0001134	absent corpus luteum	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	either: 129 or (involves: 129S7/SvEvBrd * C57BL/6)	N	7885474
MGI:2450545	M	MP:0004852	decreased testis weight	Arl4a<tm1Asch>/Arl4a<tm1Asch>	involves: C57BL/6J	N	11909968
MGI:2450545	M	MP:0004901	decreased male germ cell number	Arl4a<tm1Asch>/Arl4a<tm1Asch>	involves: C57BL/6J	N	11909968
MGI:2450545	M	MP:0001156	abnormal spermatogenesis	Arl4a<tm1Asch>/Arl4a<tm1Asch>	involves: C57BL/6J	N	11909968
MGI:2450545	M	MP:0002687	oligozoospermia	Arl4a<tm1Asch>/Arl4a<tm1Asch>	involves: C57BL/6J	N	11909968
MGI:2450547	F	MP:0001926	female infertility	Ambp<tm1Miya>/Ambp<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	11243855
MGI:2450547	F	MP:0001923	reduced female fertility	Ambp<tm1Miya>/Ambp<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	11243855
MGI:2450547	F	MP:0003697	absent zona pellucida	Ambp<tm1Miya>/Ambp<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	11243855
MGI:2450547	F	MP:0009648	abnormal superovulation	Ambp<tm1Miya>/Ambp<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	11243855
MGI:2450547	F	MP:0001125	abnormal oocyte morphology	Ambp<tm1Miya>/Ambp<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	11243855
MGI:2450556	F	MP:0001923	reduced female fertility	Ambp<tm1Kkm>/Ambp<tm1Kkm>	involves: 129P2/OlaHsd * C57BL/6	N	11145954
MGI:2450556	F	MP:0001926	female infertility	Ambp<tm1Kkm>/Ambp<tm1Kkm>	involves: 129P2/OlaHsd * C57BL/6	N	11145954
MGI:2450556	F	MP:0009374	absent cumulus expansion	Ambp<tm1Kkm>/Ambp<tm1Kkm>	involves: 129P2/OlaHsd * C57BL/6	N	11145954
MGI:2450556	F	MP:0001125	abnormal oocyte morphology	Ambp<tm1Kkm>/Ambp<tm1Kkm>	involves: 129P2/OlaHsd * C57BL/6	N	11145954
MGI:2450556	F	MP:0001386	abnormal maternal nurturing	Ambp<tm1Kkm>/Ambp<tm1Kkm>	involves: 129P2/OlaHsd * C57BL/6	N	11145954
MGI:2450563	M	MP:0031012	impaired sperm migration in female genital tract	Ace<tm1Unc>/Ace<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	9482924
MGI:2450563	M	MP:0005389	reproductive system phenotype	Ace<tm1Unc>/Ace<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	Y	9482924
MGI:2450563	M	MP:0001922	reduced male fertility	Ace<tm1Unc>/Ace<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	7753170
MGI:2450563	M	MP:0030978	impaired binding of sperm to zona pellucida	Ace<tm1Unc>/Ace<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	9482924
MGI:2450564	M	MP:0001596	hypotension	Ace<tm1Unc>/Ace<+>	involves: 129P2/OlaHsd * C57BL/6J	N	7753170
MGI:2450564	M	MP:0005389	reproductive system phenotype	Ace<tm1Unc>/Ace<+>	involves: 129P2/OlaHsd * C57BL/6J	Y	9482924
MGI:2450604	M	MP:0002631	abnormal epididymis morphology	Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	9463357
MGI:2450604	M	MP:0001154	seminiferous tubule degeneration	Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	9463357
MGI:2450604	M	MP:0014052	increased male germ cell apoptosis	Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	9463357
MGI:2450604	M	MP:0001932	abnormal spermiogenesis	Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	9463357
MGI:2450604	M	MP:0001922	reduced male fertility	Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	9463357
MGI:2450604	M	MP:0001156	abnormal spermatogenesis	Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	9463357
MGI:2450604	M	MP:0004934	epididymis epithelium degeneration	Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S6/SvEvTac * Black Swiss	N	9463357
MGI:2450605	M	MP:0004934	epididymis epithelium degeneration	Bmp8a<tm1Blh>/Bmp8a<+>,Bmp8b<tm1Blh>/Bmp8b<+>	involves: 129/Sv * 129S6/SvEvTac * Black Swiss	N	9463357
MGI:2450605	M	MP:0001156	abnormal spermatogenesis	Bmp8a<tm1Blh>/Bmp8a<+>,Bmp8b<tm1Blh>/Bmp8b<+>	involves: 129/Sv * 129S6/SvEvTac * Black Swiss	N	9463357
MGI:2450605	M	MP:0006362	abnormal male germ cell morphology	Bmp8a<tm1Blh>/Bmp8a<+>,Bmp8b<tm1Blh>/Bmp8b<+>	involves: 129/Sv * 129S6/SvEvTac * Black Swiss	N	9463357
MGI:2450606	M	MP:0001156	abnormal spermatogenesis	Bmp8a<tm1Blh>/Bmp8a<+>	involves: 129S6/SvEvTac * Black Swiss	N	9463357
MGI:2450606	M	MP:0006362	abnormal male germ cell morphology	Bmp8a<tm1Blh>/Bmp8a<+>	involves: 129S6/SvEvTac * Black Swiss	N	9463357
MGI:2450673	F	MP:0001923	reduced female fertility	Abca1<tm1Wpfl>/Abca1<tm1Wpfl>	involves: 129P2/OlaHsd * C57BL/6J	N	10980140
MGI:2450673	M	MP:0002784	abnormal Sertoli cell morphology	Abca1<tm1Wpfl>/Abca1<tm1Wpfl>	involves: 129P2/OlaHsd * C57BL/6J	N	10980140
MGI:2450673	F	MP:0001120	abnormal uterus morphology	Abca1<tm1Wpfl>/Abca1<tm1Wpfl>	involves: 129P2/OlaHsd * C57BL/6J	N	10980140
MGI:2450673	F	MP:0001126	abnormal ovary morphology	Abca1<tm1Wpfl>/Abca1<tm1Wpfl>	involves: 129P2/OlaHsd * C57BL/6J	N	10980140
MGI:2450674	F	MP:0001923	reduced female fertility	Abca1<tm1Wpfl>/Abca1<+>	involves: 129P2/OlaHsd * C57BL/6J	N	10980140
MGI:2450723	F	MP:0001926	female infertility	Abca1<tm1Jdm>/Abca1<tm1Jdm>	DBA/1LacJ-Abca1<tm1Jdm>	N	10878804
MGI:2450751	F	MP:0011121	decreased primordial ovarian follicle number	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17207475
MGI:2450751	F	MP:0011127	abnormal tertiary ovarian follicle number	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17207475
MGI:2450751	F	MP:0011129	decreased tertiary ovarian follicle number	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17207475
MGI:2450751	F	MP:0003378	early sexual maturation	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19684329
MGI:2450751	F	MP:0001127	small ovary	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11557891
MGI:2450751	F	MP:0001750	increased circulating follicle stimulating hormone level	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19684329
MGI:2450751	F	MP:0031018	decreased granulosa cell proliferation	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17207475
MGI:2450751	F	MP:0031381	decreased secondary ovarian follicle number	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17207475
MGI:2450751	F	MP:0031020	premature ovarian failure	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19684329
MGI:2450751	F	MP:0009017	prolonged estrus	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19684329
MGI:2450751	F	MP:0013236	ovary degeneration	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19684329
MGI:2450751	F	MP:0005431	decreased oocyte number	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19684329
MGI:2450751	F	MP:0009648	abnormal superovulation	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11557891
MGI:2450751	F	MP:0013508	increased granulosa cell apoptosis	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17207475
MGI:2450751	F	MP:0002016	ovary cyst	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19684329
MGI:2450751	F	MP:0001927	abnormal estrous cycle	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19684329
MGI:2450751	F	MP:0002777	absent ovarian follicles	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19684329
MGI:2450751	F	MP:0001926	female infertility	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11557891
MGI:2450751	F	MP:0001125	abnormal oocyte morphology	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11557891
MGI:2450751	F	MP:0001125	abnormal oocyte morphology	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19684329
MGI:2450751	F	MP:0001129	impaired ovarian folliculogenesis	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17207475
MGI:2450751	F	MP:0001129	impaired ovarian folliculogenesis	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11557891
MGI:2450751	F	MP:0001132	absent mature ovarian follicles	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11557891
MGI:2450751	F	MP:0031239	increased atretic ovarian follicle number	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17207475
MGI:2450836	F	MP:0001120	abnormal uterus morphology	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	N	9396142
MGI:2450836	F	MP:0001923	reduced female fertility	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	N	9396142
MGI:2450857	M	MP:0031408	multi-headed sperm	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0009230	abnormal sperm head morphology	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0002687	oligozoospermia	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0002675	asthenozoospermia	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0006379	abnormal spermatocyte morphology	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0009232	abnormal sperm nucleus morphology	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0020550	multinucleated giant male germ cells	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0008892	abnormal sperm flagellum morphology	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0002686	globozoospermia	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0005578	teratozoospermia	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0009839	multiflagellated sperm	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0001156	abnormal spermatogenesis	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0008545	absent sperm flagellum	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0004182	abnormal spermiation	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0001932	abnormal spermiogenesis	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0001922	reduced male fertility	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450857	M	MP:0008898	abnormal acrosome morphology	Gmcl1<tm1Nkn>/Gmcl1<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	12556490
MGI:2450873	M	MP:0001156	abnormal spermatogenesis	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N)	N	12556476
MGI:2450873	M	MP:0005169	abnormal male meiosis	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N)	N	12556476
MGI:2450873	M	MP:0001925	male infertility	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N)	N	12556476
MGI:2450873	M	MP:0006379	abnormal spermatocyte morphology	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N)	N	12556476
MGI:2450873	M	MP:0010207	abnormal telomere morphology	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N)	N	12556476
MGI:2450873	M	MP:0014052	increased male germ cell apoptosis	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N)	N	12556476
MGI:2450873	M	MP:0009452	abnormal synaptonemal complex	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N)	N	12556476
MGI:2450995	M	MP:0009838	abnormal sperm axoneme morphology	Spmap2<Tg(PDE5A)1Ynk>/Spmap2<Tg(PDE5A)1Ynk>	involves: C3H	N	10747865
MGI:2450995	M	MP:0002675	asthenozoospermia	Spmap2<Tg(PDE5A)1Ynk>/Spmap2<Tg(PDE5A)1Ynk>	involves: C3H	N	10747865
MGI:2450995	M	MP:0004901	decreased male germ cell number	Spmap2<Tg(PDE5A)1Ynk>/Spmap2<Tg(PDE5A)1Ynk>	involves: C3H	N	10747865
MGI:2450995	M	MP:0005578	teratozoospermia	Spmap2<Tg(PDE5A)1Ynk>/Spmap2<Tg(PDE5A)1Ynk>	involves: C3H	N	10747865
MGI:2450995	M	MP:0006380	abnormal spermatid morphology	Spmap2<Tg(PDE5A)1Ynk>/Spmap2<Tg(PDE5A)1Ynk>	involves: C3H	N	10747865
MGI:2450995	M	MP:0004852	decreased testis weight	Spmap2<Tg(PDE5A)1Ynk>/Spmap2<Tg(PDE5A)1Ynk>	involves: C3H	N	10747865
MGI:2450995	M	MP:0008892	abnormal sperm flagellum morphology	Spmap2<Tg(PDE5A)1Ynk>/Spmap2<Tg(PDE5A)1Ynk>	involves: C3H	N	10747865
MGI:2450995	M	MP:0005159	azoospermia	Spmap2<Tg(PDE5A)1Ynk>/Spmap2<Tg(PDE5A)1Ynk>	involves: C3H	N	10747865
MGI:2450995	M	MP:0009232	abnormal sperm nucleus morphology	Spmap2<Tg(PDE5A)1Ynk>/Spmap2<Tg(PDE5A)1Ynk>	involves: C3H	N	10747865
MGI:2450995	M	MP:0001925	male infertility	Spmap2<Tg(PDE5A)1Ynk>/Spmap2<Tg(PDE5A)1Ynk>	involves: C3H	N	10747865
MGI:2450995	M	MP:0008545	absent sperm flagellum	Spmap2<Tg(PDE5A)1Ynk>/Spmap2<Tg(PDE5A)1Ynk>	involves: C3H	N	10747865
MGI:2451017	M	MP:0000755	hindlimb paralysis	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451017	M	MP:0005150	cachexia	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451017	M	MP:0001954	respiratory distress	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451017	M	MP:0009422	decreased gastrocnemius weight	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	22068590
MGI:2451017	M	MP:0001732	postnatal growth retardation	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451017	M	MP:0010053	decreased grip strength	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	22068590
MGI:2451017	M	MP:0000160	kyphosis	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451017	M	MP:0002757	decreased vertical activity	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	22068590
MGI:2451017	M	MP:0002269	muscular atrophy	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451017	M	MP:0003084	abnormal skeletal muscle fiber morphology	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451017	M	MP:0000751	myopathy	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451017	M	MP:0002106	abnormal muscle physiology	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451017	M	MP:0001402	decreased locomotor activity	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	22068590
MGI:2451017	M	MP:0009417	skeletal muscle atrophy	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	22068590
MGI:2451017	M	MP:0004262	abnormal physical strength	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451017	M	MP:0000748	progressive muscle weakness	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	22068590
MGI:2451017	M	MP:0000748	progressive muscle weakness	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451017	M	MP:0002066	abnormal motor capabilities/coordination/movement	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451017	M	MP:0002083	premature death	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	22068590
MGI:2451017	M	MP:0002083	premature death	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451017	M	MP:0011090	perinatal lethality, incomplete penetrance	Mtm1<tm1.1Jman>/Y	involves: 129T1/Sv * C57BL/6	N	12391329
MGI:2451045	M	MP:0001925	male infertility	Tpgs1<Gt(ROSA22)Sor>/Tpgs1<Gt(ROSA22)Sor>	involves: 129S/SvEv * C57BL/6	N	12242242
MGI:2451045	M	MP:0001932	abnormal spermiogenesis	Tpgs1<Gt(ROSA22)Sor>/Tpgs1<Gt(ROSA22)Sor>	involves: 129S/SvEv * C57BL/6	N	12242242
MGI:2451045	M	MP:0005578	teratozoospermia	Tpgs1<Gt(ROSA22)Sor>/Tpgs1<Gt(ROSA22)Sor>	involves: 129S/SvEv * C57BL/6	N	12242242
MGI:2451045	M	MP:0009838	abnormal sperm axoneme morphology	Tpgs1<Gt(ROSA22)Sor>/Tpgs1<Gt(ROSA22)Sor>	involves: 129S/SvEv * C57BL/6	N	12242242
MGI:2451045	M	MP:0031352	absent sperm axonemal central pair	Tpgs1<Gt(ROSA22)Sor>/Tpgs1<Gt(ROSA22)Sor>	involves: 129S/SvEv * C57BL/6	N	12242242
MGI:2451045	M	MP:0008545	absent sperm flagellum	Tpgs1<Gt(ROSA22)Sor>/Tpgs1<Gt(ROSA22)Sor>	involves: 129S/SvEv * C57BL/6	N	12242242
MGI:2451053	M	MP:0004935	epididymis degeneration	Bmp7<tm1Rob>/Bmp7<+>,Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S/SvEv * 129S6/SvEvTac * Black Swiss * C57BL/6	N	11784057
MGI:2451053	M	MP:0006362	abnormal male germ cell morphology	Bmp7<tm1Rob>/Bmp7<+>,Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S/SvEv * 129S6/SvEvTac * Black Swiss * C57BL/6	N	11784057
MGI:2451053	M	MP:0002631	abnormal epididymis morphology	Bmp7<tm1Rob>/Bmp7<+>,Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S/SvEv * 129S6/SvEvTac * Black Swiss * C57BL/6	N	11784057
MGI:2451053	M	MP:0001156	abnormal spermatogenesis	Bmp7<tm1Rob>/Bmp7<+>,Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S/SvEv * 129S6/SvEvTac * Black Swiss * C57BL/6	N	11784057
MGI:2451053	M	MP:0001925	male infertility	Bmp7<tm1Rob>/Bmp7<+>,Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S/SvEv * 129S6/SvEvTac * Black Swiss * C57BL/6	N	11784057
MGI:2451053	M	MP:0004934	epididymis epithelium degeneration	Bmp7<tm1Rob>/Bmp7<+>,Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S/SvEv * 129S6/SvEvTac * Black Swiss * C57BL/6	N	11784057
MGI:2451055	M	MP:0002631	abnormal epididymis morphology	Bmp7<tm1Rob>/Bmp7<+>,Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S/SvEv * 129S6/SvEvTac * Black Swiss	N	11784057
MGI:2451055	M	MP:0004852	decreased testis weight	Bmp7<tm1Rob>/Bmp7<+>,Bmp8a<tm1Blh>/Bmp8a<tm1Blh>	involves: 129S/SvEv * 129S6/SvEvTac * Black Swiss	N	11784057
MGI:2451094	M	MP:0001153	small seminiferous tubules	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	8682296
MGI:2451094	M	MP:0002685	abnormal spermatogonia proliferation	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	8682296
MGI:2451094	M	MP:0001147	small testis	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	9463357
MGI:2451094	M	MP:0001154	seminiferous tubule degeneration	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	8682296
MGI:2451094	M	MP:0001154	seminiferous tubule degeneration	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	9463357
MGI:2451094	M	MP:0014052	increased male germ cell apoptosis	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	8682296
MGI:2451094	M	MP:0006362	abnormal male germ cell morphology	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	8682296
MGI:2451094	M	MP:0001152	increased Leydig cell number	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	8682296
MGI:2451094	M	MP:0001156	abnormal spermatogenesis	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	8682296
MGI:2451094	M	MP:0001147	small testis	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	8682296
MGI:2451094	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	8682296
MGI:2451094	M	MP:0004852	decreased testis weight	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	8682296
MGI:2451094	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	9463357
MGI:2451094	M	MP:0013600	testis degeneration	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	8682296
MGI:2451094	M	MP:0004901	decreased male germ cell number	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	8682296
MGI:2451094	M	MP:0001925	male infertility	Bmp8b<tm1Blh>/Bmp8b<tm1Blh>	involves: 129/Sv * Black Swiss	N	8682296
MGI:2451124	F	MP:0011120	increased primordial ovarian follicle number	Casp2<tm1Yuan>/Casp2<tm1Yuan>	involves: 129S4/SvJae * C57BL/6J * DBA/2	N	9573047
MGI:2451124	F	MP:0001125	abnormal oocyte morphology	Casp2<tm1Yuan>/Casp2<tm1Yuan>	involves: 129S4/SvJae * C57BL/6J * DBA/2	N	9573047
MGI:2451124	F	MP:0006361	abnormal female germ cell morphology	Casp2<tm1Yuan>/Casp2<tm1Yuan>	involves: 129S4/SvJae * C57BL/6J * DBA/2	N	9573047
MGI:2451130	F	MP:0001923	reduced female fertility	Cd9<tm1Bcx>/Cd9<tm1Bcx>	involves: 129P2/OlaHsd * C57BL/6	N	10634790
MGI:2451150	M	MP:0004901	decreased male germ cell number	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	10932193
MGI:2451150	M	MP:0008892	abnormal sperm flagellum morphology	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	10932193
MGI:2451150	F	MP:0008869	anovulation	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	11108293
MGI:2451150	M	MP:0004852	decreased testis weight	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	10932193
MGI:2451150	M	MP:0005578	teratozoospermia	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	10932193
MGI:2451150	F	MP:0009433	polyovular ovarian follicle	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	11108293
MGI:2451150	M	MP:0002687	oligozoospermia	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	10932193
MGI:2451150	F	MP:0001923	reduced female fertility	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	11108293
MGI:2451150	M	MP:0001154	seminiferous tubule degeneration	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	10932193
MGI:2451150	F	MP:0001131	abnormal ovarian follicle morphology	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	11108293
MGI:2451150	F	MP:0001119	abnormal female reproductive system morphology	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	11108293
MGI:2451150	F	MP:0001134	absent corpus luteum	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	11108293
MGI:2451150	M	MP:0001145	abnormal male reproductive system morphology	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	10932193
MGI:2451150	M	MP:0001925	male infertility	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	10932193
MGI:2451150	M	MP:0001932	abnormal spermiogenesis	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	10932193
MGI:2451150	M	MP:0006380	abnormal spermatid morphology	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	10932193
MGI:2451150	M	MP:0009230	abnormal sperm head morphology	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	10932193
MGI:2451150	M	MP:0001155	arrest of spermatogenesis	Camk4<tm1Arm>/Camk4<tm1Arm>	involves: 129 * C57BL/6J	N	10932193
MGI:2451152	M	MP:0001925	male infertility	Clgn<tm1Osb>/Clgn<tm1Osb>	either: 129 or (involves: 129P2/OlaHsd * C57BL/6J)	N	9177349
MGI:2451152	M	MP:0005389	reproductive system phenotype	Clgn<tm1Osb>/Clgn<tm1Osb>	either: 129 or (involves: 129P2/OlaHsd * C57BL/6J)	Y	9177349
MGI:2451152	M	MP:0030978	impaired binding of sperm to zona pellucida	Clgn<tm1Osb>/Clgn<tm1Osb>	either: 129 or (involves: 129P2/OlaHsd * C57BL/6J)	N	9177349
MGI:2451166	M	MP:0009237	kinked sperm flagellum	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	10471512
MGI:2451166	M	MP:0009232	abnormal sperm nucleus morphology	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	10471512
MGI:2451166	M	MP:0009231	detached acrosome	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	12950107
MGI:2451166	M	MP:0009231	detached acrosome	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	10471512
MGI:2451166	M	MP:0001932	abnormal spermiogenesis	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	12950107
MGI:2451166	M	MP:0002687	oligozoospermia	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	12950107
MGI:2451166	M	MP:0006380	abnormal spermatid morphology	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	10471512
MGI:2451166	M	MP:0005578	teratozoospermia	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	10471512
MGI:2451166	M	MP:0006379	abnormal spermatocyte morphology	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	12950107
MGI:2451166	M	MP:0009230	abnormal sperm head morphology	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	10471512
MGI:2451166	M	MP:0009238	coiled sperm flagellum	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	12950107
MGI:2451166	M	MP:0006380	abnormal spermatid morphology	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	12950107
MGI:2451166	M	MP:0009237	kinked sperm flagellum	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	12950107
MGI:2451166	M	MP:0006378	abnormal spermatogonia morphology	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	12950107
MGI:2451166	M	MP:0008898	abnormal acrosome morphology	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	12950107
MGI:2451166	M	MP:0001156	abnormal spermatogenesis	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	12950107
MGI:2451166	M	MP:0002674	abnormal sperm motility	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	10471512
MGI:2451166	M	MP:0001925	male infertility	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	10471512
MGI:2451166	M	MP:0002687	oligozoospermia	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	10471512
MGI:2451166	M	MP:0014052	increased male germ cell apoptosis	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	10471512
MGI:2451166	M	MP:0002686	globozoospermia	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	N	10471512
MGI:2451221	F	MP:0001923	reduced female fertility	Pde4d<tm1Mct>/Pde4d<tm1Mct>	involves: 129P2/OlaHsd * C57BL/6	N	10518565
MGI:2451221	F	MP:0031420	decreased superovulation rate	Pde4d<tm1Mct>/Pde4d<tm1Mct>	involves: 129P2/OlaHsd * C57BL/6	N	10518565
MGI:2451237	M	MP:0000832	abnormal thalamus morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0002741	small olfactory bulb	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0008128	abnormal brain internal capsule morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0006009	abnormal neuronal migration	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0008929	abnormal central medial nucleus morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0008223	absent hippocampal commissure	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0000787	abnormal telencephalon morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0000808	abnormal hippocampus development	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0013603	abnormal fetal Leydig cell differentiation	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0008439	abnormal cortical plate morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0000812	abnormal dentate gyrus morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0003232	abnormal forebrain development	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0000792	abnormal cortical marginal zone morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0003247	abnormal glutaminergic neuron morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0001147	small testis	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0008536	enlarged third ventricle	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0000934	abnormal telencephalon development	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0000780	abnormal corpus callosum morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0011087	neonatal lethality, complete penetrance	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0000819	abnormal olfactory bulb morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0008547	abnormal neocortex morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0008267	abnormal hippocampus CA3 region morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0000774	decreased brain size	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0008458	abnormal cortical ventricular zone morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0009324	absent hippocampal fimbria	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0008441	thin cortical plate	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0000778	abnormal nervous system tract morphology	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0006308	enlarged seminiferous tubules	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451237	M	MP:0005148	seminal vesicle hypoplasia	Arx<tm1Kki>/Y	involves: 129P2/OlaHsd * C57BL	N	12379852
MGI:2451359	F	MP:0009069	dilated oviduct	Cbl<tm1Wlan>/Cbl<tm1Wlan>	involves: 129S1/Sv * C57BL/6	N	12591907
MGI:2451359	F	MP:0001123	dilated uterus	Cbl<tm1Wlan>/Cbl<tm1Wlan>	involves: 129S1/Sv * C57BL/6	N	12591907
MGI:2651405	F	MP:0002679	abnormal corpus luteum morphology	Gja4<tm1Paul>/Gja4<tm1Paul>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	9020357
MGI:2651405	F	MP:0008869	anovulation	Gja4<tm1Paul>/Gja4<tm1Paul>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	9020357
MGI:2651405	F	MP:0001926	female infertility	Gja4<tm1Paul>/Gja4<tm1Paul>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	9020357
MGI:2651405	F	MP:0005168	abnormal female meiosis	Gja4<tm1Paul>/Gja4<tm1Paul>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	9020357
MGI:2651548	F	MP:0003534	blind vagina	Pax2<tm1Mbu>/Pax2<+>,Pax8<tm1(cre)Mbu>/Pax8<+>	involves: 129P2/OlaHsd * C3H/He * C57BL/6	N	12435636
MGI:2651548	M	MP:0001922	reduced male fertility	Pax2<tm1Mbu>/Pax2<+>,Pax8<tm1(cre)Mbu>/Pax8<+>	involves: 129P2/OlaHsd * C3H/He * C57BL/6	N	12435636
MGI:2651548	F	MP:0001144	vagina atresia	Pax2<tm1Mbu>/Pax2<+>,Pax8<tm1(cre)Mbu>/Pax8<+>	involves: 129P2/OlaHsd * C3H/He * C57BL/6	N	12435636
MGI:2651673	F	MP:0008522	abnormal lymph node germinal center morphology	Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2651673	F	MP:0008186	increased pro-B cell number	Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * C57BL/6	N	7552994
MGI:2651673	F	MP:0002144	abnormal B cell differentiation	Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * C57BL/6	N	7552994
MGI:2651673	F	MP:0001806	decreased IgM level	Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2651673	F	MP:0001806	decreased IgM level	Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * C57BL/6	N	7552994
MGI:2651673	F	MP:0005093	decreased B cell proliferation	Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2651673	F	MP:0008211	decreased mature B cell number	Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * C57BL/6	N	7552994
MGI:2651673	F	MP:0008211	decreased mature B cell number	Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2651673	F	MP:0008498	decreased IgG3 level	Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2651673	F	MP:0008498	decreased IgG3 level	Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * C57BL/6	N	7552994
MGI:2651673	F	MP:0008217	abnormal B cell activation	Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * C57BL/6	N	7552994
MGI:2651673	F	MP:0008482	decreased spleen germinal center number	Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2651673	F	MP:0008484	decreased spleen germinal center size	Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2651696	M	MP:0001925	male infertility	Atxn7<tm1Hzo>/Atxn7<+>	involves: 129S7/SvEvBrd * C57BL/6	N	12575948
MGI:2651696	F	MP:0001926	female infertility	Atxn7<tm1Hzo>/Atxn7<+>	involves: 129S7/SvEvBrd * C57BL/6	N	12575948
MGI:2652039	F	MP:0001129	impaired ovarian folliculogenesis	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>	involves: 129S7/SvEvBrd	N	11376106
MGI:2652039	F	MP:0001923	reduced female fertility	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>	involves: 129S7/SvEvBrd	N	11376106
MGI:2652039	F	MP:0002016	ovary cyst	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>	involves: 129S7/SvEvBrd	N	11376106
MGI:2652039	F	MP:0003696	abnormal zona pellucida morphology	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>	involves: 129S7/SvEvBrd	N	11376106
MGI:2652039	F	MP:0001935	decreased litter size	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>	involves: 129S7/SvEvBrd	N	11376106
MGI:2652040	F	MP:0001130	abnormal ovarian folliculogenesis	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652040	F	MP:0005431	decreased oocyte number	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652040	F	MP:0003696	abnormal zona pellucida morphology	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652040	F	MP:0001923	reduced female fertility	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652040	F	MP:0001125	abnormal oocyte morphology	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652040	F	MP:0031420	decreased superovulation rate	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652040	F	MP:0001935	decreased litter size	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652040	F	MP:0002016	ovary cyst	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652042	F	MP:0003696	abnormal zona pellucida morphology	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652042	F	MP:0001923	reduced female fertility	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652042	F	MP:0009374	absent cumulus expansion	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652042	F	MP:0001935	decreased litter size	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652042	F	MP:0001134	absent corpus luteum	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652042	F	MP:0005431	decreased oocyte number	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652042	F	MP:0009433	polyovular ovarian follicle	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652042	F	MP:0001125	abnormal oocyte morphology	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652042	F	MP:0002682	decreased mature ovarian follicle number	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	11376106
MGI:2652043	F	MP:0005431	decreased oocyte number	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd	N	11376106
MGI:2652043	F	MP:0009374	absent cumulus expansion	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd	N	11376106
MGI:2652043	F	MP:0001134	absent corpus luteum	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd	N	11376106
MGI:2652043	F	MP:0001125	abnormal oocyte morphology	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd	N	11376106
MGI:2652043	F	MP:0002682	decreased mature ovarian follicle number	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd	N	11376106
MGI:2652043	F	MP:0001926	female infertility	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd	N	11376106
MGI:2652043	F	MP:0009433	polyovular ovarian follicle	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd	N	11376106
MGI:2652043	F	MP:0003696	abnormal zona pellucida morphology	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<+>	involves: 129S7/SvEvBrd	N	11376106
MGI:2652044	F	MP:0002016	ovary cyst	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	11376106
MGI:2652044	F	MP:0001126	abnormal ovary morphology	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	11376106
MGI:2652044	F	MP:0003696	abnormal zona pellucida morphology	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	11376106
MGI:2652044	F	MP:0004805	absent oocytes	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	11376106
MGI:2652044	F	MP:0001926	female infertility	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	11376106
MGI:2652044	F	MP:0001129	impaired ovarian folliculogenesis	Bmp15<tm1Zuk>/Bmp15<tm1Zuk>,Gdf9<tm1Zuk>/Gdf9<tm1Zuk>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	11376106
MGI:2652046	M	MP:0005389	reproductive system phenotype	Bmp15<tm1Zuk>/Y	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	Y	11376106
MGI:2652055	M	MP:0004542	impaired acrosome reaction	Smcp<tm1Wen>/Smcp<tm1Wen>	involves: 129S1/Sv * 129X1/SvJ	N	11940662
MGI:2652055	M	MP:0030976	impaired sperm penetration of zona pellucida	Smcp<tm1Wen>/Smcp<tm1Wen>	involves: 129S1/Sv * 129X1/SvJ	N	11940662
MGI:2652055	M	MP:0001925	male infertility	Smcp<tm1Wen>/Smcp<tm1Wen>	involves: 129S1/Sv * 129X1/SvJ	N	11940662
MGI:2652055	M	MP:0002675	asthenozoospermia	Smcp<tm1Wen>/Smcp<tm1Wen>	involves: 129S1/Sv * 129X1/SvJ	N	11940662
MGI:2652088	M	MP:0001156	abnormal spermatogenesis	Acox1<tm1Jkr>/Acox1<tm1Jkr>	involves: 129P2/OlaHsd * C57BL/6J	N	8798738
MGI:2652088	F	MP:0001926	female infertility	Acox1<tm1Jkr>/Acox1<tm1Jkr>	involves: 129P2/OlaHsd * C57BL/6J	N	8798738
MGI:2652088	M	MP:0001925	male infertility	Acox1<tm1Jkr>/Acox1<tm1Jkr>	involves: 129P2/OlaHsd * C57BL/6J	N	8798738
MGI:2652088	M	MP:0001147	small testis	Acox1<tm1Jkr>/Acox1<tm1Jkr>	involves: 129P2/OlaHsd * C57BL/6J	N	8798738
MGI:2652088	F	MP:0001127	small ovary	Acox1<tm1Jkr>/Acox1<tm1Jkr>	involves: 129P2/OlaHsd * C57BL/6J	N	8798738
MGI:2652088	M	MP:0006380	abnormal spermatid morphology	Acox1<tm1Jkr>/Acox1<tm1Jkr>	involves: 129P2/OlaHsd * C57BL/6J	N	8798738
MGI:2652088	M	MP:0005536	decreased Leydig cell number	Acox1<tm1Jkr>/Acox1<tm1Jkr>	involves: 129P2/OlaHsd * C57BL/6J	N	8798738
MGI:2652097	F	MP:0001382	abnormal nursing	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652097	F	MP:0006270	abnormal mammary gland growth during lactation	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652097	M	MP:0031410	biflagellated sperm	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652097	M	MP:0030590	abnormal sperm fibrous sheath morphology	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652097	F	MP:0013716	hypolactation	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652097	M	MP:0002675	asthenozoospermia	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652097	M	MP:0009830	abnormal sperm connecting piece morphology	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652097	M	MP:0006380	abnormal spermatid morphology	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652097	M	MP:0005578	teratozoospermia	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652097	F	MP:0006269	abnormal mammary gland growth during pregnancy	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652097	M	MP:0009838	abnormal sperm axoneme morphology	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652097	M	MP:0001925	male infertility	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652097	M	MP:0009234	absent sperm head	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652097	F	MP:0004047	abnormal milk composition	Neurl1a<tm1Led>/Neurl1a<tm1Led>	involves: 129S6/SvEvTac	N	11585928
MGI:2652543	F	MP:0001802	arrested B cell differentiation	Blnk<tm1Pjln>/Blnk<tm1Pjln>,Btk<tm1Wk>/Btk<tm1Wk>	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11449370
MGI:2652551	M	MP:0004852	decreased testis weight	Papolb<tm1Tba>/Papolb<tm1Tba>	involves: 129S2/SvPas * C57BL/6	N	12471261
MGI:2652551	M	MP:0014052	increased male germ cell apoptosis	Papolb<tm1Tba>/Papolb<tm1Tba>	involves: 129S2/SvPas * C57BL/6	N	12471261
MGI:2652551	M	MP:0001155	arrest of spermatogenesis	Papolb<tm1Tba>/Papolb<tm1Tba>	involves: 129S2/SvPas * C57BL/6	N	12471261
MGI:2652551	M	MP:0001153	small seminiferous tubules	Papolb<tm1Tba>/Papolb<tm1Tba>	involves: 129S2/SvPas * C57BL/6	N	12471261
MGI:2652551	M	MP:0001925	male infertility	Papolb<tm1Tba>/Papolb<tm1Tba>	involves: 129S2/SvPas * C57BL/6	N	12471261
MGI:2652604	M	MP:0001147	small testis	Snai2<tm2Grid>/Snai2<tm2Grid>	involves: 129S1/Sv	N	12149208
MGI:2652604	M	MP:0001922	reduced male fertility	Snai2<tm2Grid>/Snai2<tm2Grid>	involves: 129S1/Sv	N	12149208
MGI:2652604	M	MP:0001925	male infertility	Snai2<tm2Grid>/Snai2<tm2Grid>	involves: 129S1/Sv	N	12149208
MGI:2652604	M	MP:0001153	small seminiferous tubules	Snai2<tm2Grid>/Snai2<tm2Grid>	involves: 129S1/Sv	N	12149208
MGI:2652689	F	MP:0003356	impaired luteinization	Csf2<tm1Ard>/Csf2<tm1Ard>	involves: 129P2/OlaHsd * C57BL/6	N	10684813
MGI:2652689	F	MP:0001132	absent mature ovarian follicles	Csf2<tm1Ard>/Csf2<tm1Ard>	involves: 129P2/OlaHsd * C57BL/6	N	10684813
MGI:2652689	F	MP:0001928	abnormal ovulation	Csf2<tm1Ard>/Csf2<tm1Ard>	involves: 129P2/OlaHsd * C57BL/6	N	10684813
MGI:2652689	F	MP:0009011	prolonged diestrus	Csf2<tm1Ard>/Csf2<tm1Ard>	involves: 129P2/OlaHsd * C57BL/6	N	10684813
MGI:2652689	F	MP:0001120	abnormal uterus morphology	Csf2<tm1Ard>/Csf2<tm1Ard>	involves: 129P2/OlaHsd * C57BL/6	N	9915988
MGI:2652689	F	MP:0004856	decreased ovary weight	Csf2<tm1Ard>/Csf2<tm1Ard>	involves: 129P2/OlaHsd * C57BL/6	N	10684813
MGI:2652689	F	MP:0009006	prolonged estrous cycle	Csf2<tm1Ard>/Csf2<tm1Ard>	involves: 129P2/OlaHsd * C57BL/6	N	10684813
MGI:2652689	F	MP:0009020	prolonged metestrus	Csf2<tm1Ard>/Csf2<tm1Ard>	involves: 129P2/OlaHsd * C57BL/6	N	10684813
MGI:2652724	F	MP:0005559	increased circulating glucose level	Lipe<tm1Gam>/Lipe<tm1Gam>	involves: 129S4/SvJae * BALB/c	N	11316346
MGI:2652724	F	MP:0005668	decreased circulating leptin level	Lipe<tm1Gam>/Lipe<tm1Gam>	involves: 129S4/SvJae * BALB/c	N	11316346
MGI:2652724	M	MP:0001553	abnormal circulating free fatty acids level	Lipe<tm1Gam>/Lipe<tm1Gam>	involves: 129S4/SvJae * BALB/c	N	11316346
MGI:2653033	M	MP:0001147	small testis	Htr1b<tm1Rhn>/Htr1b<tm1Rhn>	involves: 129S2/SvPas	N	11790410
MGI:2653057	F	MP:0001923	reduced female fertility	Nfia<tm1Rmg>/Nfia<tm1Rmg>	involves: 129P2/OlaHsd * Black Swiss	N	10518556
MGI:2653057	M	MP:0001925	male infertility	Nfia<tm1Rmg>/Nfia<tm1Rmg>	involves: 129P2/OlaHsd * Black Swiss	N	10518556
MGI:2653161	F	MP:0003696	abnormal zona pellucida morphology	Zp1<tm1Dean>/Zp1<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	10433913
MGI:2653161	F	MP:0001923	reduced female fertility	Zp1<tm1Dean>/Zp1<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	10433913
MGI:2653161	F	MP:0009375	thin zona pellucida	Zp1<tm1Dean>/Zp1<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	10433913
MGI:2653161	F	MP:0001130	abnormal ovarian folliculogenesis	Zp1<tm1Dean>/Zp1<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	10433913
MGI:2653161	F	MP:0008868	abnormal granulosa cell morphology	Zp1<tm1Dean>/Zp1<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	10433913
MGI:2653174	F	MP:0011129	decreased tertiary ovarian follicle number	Zp2<tm1Dean>/Zp2<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11245577
MGI:2653174	F	MP:0009372	abnormal cumulus oophorus morphology	Zp2<tm1Dean>/Zp2<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11245577
MGI:2653174	F	MP:0031420	decreased superovulation rate	Zp2<tm1Dean>/Zp2<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11245577
MGI:2653174	F	MP:0009375	thin zona pellucida	Zp2<tm1Dean>/Zp2<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11245577
MGI:2653174	F	MP:0001926	female infertility	Zp2<tm1Dean>/Zp2<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11245577
MGI:2653196	F	MP:0003329	amyloid beta deposits	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>,Tg(APPSWE)2576Kha/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	12402041
MGI:2653196	F	MP:0002183	gliosis	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>,Tg(APPSWE)2576Kha/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	12402041
MGI:2653287	M	MP:0001262	decreased body weight	Zfx<tm1Dcp>/Y	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653287	M	MP:0008392	decreased primordial germ cell number	Zfx<tm1Dcp>/Y	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653287	M	MP:0001698	decreased embryo size	Zfx<tm1Dcp>/Y	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653287	M	MP:0002687	oligozoospermia	Zfx<tm1Dcp>/Y	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653287	M	MP:0011088	neonatal lethality, incomplete penetrance	Zfx<tm1Dcp>/Y	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653288	M	MP:0011088	neonatal lethality, incomplete penetrance	Zfx<tm1Dcp>/Y	involves: 129S4/SvJae * C57BL/6J	N	9187153
MGI:2653288	M	MP:0011085	postnatal lethality, complete penetrance	Zfx<tm1Dcp>/Y	involves: 129S4/SvJae * C57BL/6J	N	9187153
MGI:2653289	F	MP:0011086	postnatal lethality, incomplete penetrance	Zfx<tm1Dcp>/Zfx<+>	involves: 129S4/SvJae * C57BL/6J	N	9187153
MGI:2653289	F	MP:0011088	neonatal lethality, incomplete penetrance	Zfx<tm1Dcp>/Zfx<+>	involves: 129S4/SvJae * C57BL/6J	N	9187153
MGI:2653290	F	MP:0002209	decreased germ cell number	Zfx<tm1Dcp>/Zfx<+>	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653290	F	MP:0005431	decreased oocyte number	Zfx<tm1Dcp>/Zfx<+>	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653290	F	MP:0011088	neonatal lethality, incomplete penetrance	Zfx<tm1Dcp>/Zfx<+>	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653291	F	MP:0011088	neonatal lethality, incomplete penetrance	Zfx<tm1Dcp>/Zfx<tm1Dcp>	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653291	F	MP:0005431	decreased oocyte number	Zfx<tm1Dcp>/Zfx<tm1Dcp>	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653291	F	MP:0001262	decreased body weight	Zfx<tm1Dcp>/Zfx<tm1Dcp>	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653291	F	MP:0001698	decreased embryo size	Zfx<tm1Dcp>/Zfx<tm1Dcp>	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653291	F	MP:0002682	decreased mature ovarian follicle number	Zfx<tm1Dcp>/Zfx<tm1Dcp>	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653291	F	MP:0001923	reduced female fertility	Zfx<tm1Dcp>/Zfx<tm1Dcp>	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653291	F	MP:0008392	decreased primordial germ cell number	Zfx<tm1Dcp>/Zfx<tm1Dcp>	involves: 129S4/SvJae * BALB/c	N	9187153
MGI:2653292	F	MP:0002161	abnormal fertility/fecundity	Zfx<tm1Dcp>/Zfx<tm1Dcp>	involves: 129S4/SvJae * C57BL/6J	N	9187153
MGI:2653292	F	MP:0002089	abnormal postnatal growth/weight/body size	Zfx<tm1Dcp>/Zfx<tm1Dcp>	involves: 129S4/SvJae * C57BL/6J	N	9187153
MGI:2653292	F	MP:0011088	neonatal lethality, incomplete penetrance	Zfx<tm1Dcp>/Zfx<tm1Dcp>	involves: 129S4/SvJae * C57BL/6J	N	9187153
MGI:2653292	F	MP:0002088	abnormal embryonic growth/weight/body size	Zfx<tm1Dcp>/Zfx<tm1Dcp>	involves: 129S4/SvJae * C57BL/6J	N	9187153
MGI:2653295	F	MP:0009008	delayed estrous cycle	Lepr<tm1Mgmj>/Lepr<tm1Mgmj>	B6.129-Lepr<tm1Mgmj>	N	12594516
MGI:2653295	F	MP:0001882	abnormal lactation	Lepr<tm1Mgmj>/Lepr<tm1Mgmj>	B6.129-Lepr<tm1Mgmj>	N	12594516
MGI:2653295	F	MP:0001923	reduced female fertility	Lepr<tm1Mgmj>/Lepr<tm1Mgmj>	B6.129-Lepr<tm1Mgmj>	N	12594516
MGI:2653299	M	MP:0009230	abnormal sperm head morphology	Cd59b<tm1Jha>/Cd59b<tm1Jha>	involves: 129/Sv * C57BL/6	N	16272280
MGI:2653299	M	MP:0014052	increased male germ cell apoptosis	Cd59b<tm1Jha>/Cd59b<tm1Jha>	involves: 129/Sv * C57BL/6	N	16272280
MGI:2653299	M	MP:0006362	abnormal male germ cell morphology	Cd59b<tm1Jha>/Cd59b<tm1Jha>	involves: 129/Sv * C57BL/6	N	12594949
MGI:2653299	M	MP:0009325	necrospermia	Cd59b<tm1Jha>/Cd59b<tm1Jha>	involves: 129/Sv * C57BL/6	N	16272280
MGI:2653299	M	MP:0002675	asthenozoospermia	Cd59b<tm1Jha>/Cd59b<tm1Jha>	involves: 129/Sv * C57BL/6	N	12594949
MGI:2653299	M	MP:0020550	multinucleated giant male germ cells	Cd59b<tm1Jha>/Cd59b<tm1Jha>	involves: 129/Sv * C57BL/6	N	12594949
MGI:2653299	M	MP:0009234	absent sperm head	Cd59b<tm1Jha>/Cd59b<tm1Jha>	involves: 129/Sv * C57BL/6	N	16272280
MGI:2653299	M	MP:0002687	oligozoospermia	Cd59b<tm1Jha>/Cd59b<tm1Jha>	involves: 129/Sv * C57BL/6	N	16272280
MGI:2653299	M	MP:0002687	oligozoospermia	Cd59b<tm1Jha>/Cd59b<tm1Jha>	involves: 129/Sv * C57BL/6	N	12594949
MGI:2653299	M	MP:0002216	abnormal seminiferous tubule morphology	Cd59b<tm1Jha>/Cd59b<tm1Jha>	involves: 129/Sv * C57BL/6	N	16272280
MGI:2653304	M	MP:0002123	abnormal definitive hematopoiesis	Hprt1<tm1(ACTB-Epor)Unc>/Y	involves: 129P2/OlaHsd	N	8790342
MGI:2653304	M	MP:0005397	hematopoietic system phenotype	Hprt1<tm1(ACTB-Epor)Unc>/Y	involves: 129P2/OlaHsd	Y	8790342
MGI:2653305	F	MP:0005397	hematopoietic system phenotype	Hprt1<tm1(ACTB-Epor)Unc>/Hprt1<tm1(ACTB-Epor)Unc>	involves: 129P2/OlaHsd	Y	8790342
MGI:2653305	F	MP:0002123	abnormal definitive hematopoiesis	Hprt1<tm1(ACTB-Epor)Unc>/Hprt1<tm1(ACTB-Epor)Unc>	involves: 129P2/OlaHsd	N	8790342
MGI:2653458	M	MP:0001925	male infertility	Ptdss2<Gt(KST314)Byg>/Ptdss2<Gt(KST314)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	12361952
MGI:2653458	M	MP:0001146	abnormal testis morphology	Ptdss2<Gt(KST314)Byg>/Ptdss2<Gt(KST314)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	12361952
MGI:2653458	M	MP:0001152	increased Leydig cell number	Ptdss2<Gt(KST314)Byg>/Ptdss2<Gt(KST314)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	12361952
MGI:2653458	M	MP:0003205	testicular atrophy	Ptdss2<Gt(KST314)Byg>/Ptdss2<Gt(KST314)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	12361952
MGI:2653458	M	MP:0004852	decreased testis weight	Ptdss2<Gt(KST314)Byg>/Ptdss2<Gt(KST314)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	12361952
MGI:2653493	M	MP:0005159	azoospermia	Tg(Amh-Smad4)1Tkw/0	involves: CD-1	N	12414519
MGI:2653493	M	MP:0004901	decreased male germ cell number	Tg(Amh-Smad4)1Tkw/0	involves: CD-1	N	12414519
MGI:2653493	M	MP:0001147	small testis	Tg(Amh-Smad4)1Tkw/0	involves: CD-1	N	12414519
MGI:2653493	M	MP:0001925	male infertility	Tg(Amh-Smad4)1Tkw/0	involves: CD-1	N	12414519
MGI:2653493	M	MP:0004852	decreased testis weight	Tg(Amh-Smad4)1Tkw/0	involves: CD-1	N	12414519
MGI:2653493	M	MP:0014052	increased male germ cell apoptosis	Tg(Amh-Smad4)1Tkw/0	involves: CD-1	N	12414519
MGI:2653493	M	MP:0001155	arrest of spermatogenesis	Tg(Amh-Smad4)1Tkw/0	involves: CD-1	N	12414519
MGI:2653493	M	MP:0001153	small seminiferous tubules	Tg(Amh-Smad4)1Tkw/0	involves: CD-1	N	12414519
MGI:2653493	M	MP:0001152	increased Leydig cell number	Tg(Amh-Smad4)1Tkw/0	involves: CD-1	N	12414519
MGI:2653493	M	MP:0001154	seminiferous tubule degeneration	Tg(Amh-Smad4)1Tkw/0	involves: CD-1	N	12414519
MGI:2653497	F	MP:0001926	female infertility	Zar1<tm1Zuk>/Zar1<tm1Zuk>	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	12539046
MGI:2653501	F	MP:0008973	decreased erythroid progenitor cell number	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0005016	decreased lymphocyte cell number	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0000333	decreased bone marrow cell number	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0000691	enlarged spleen	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0000691	enlarged spleen	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0002397	abnormal bone marrow morphology	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0000240	extramedullary hematopoiesis	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0002596	abnormal hematocrit	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0003179	thrombocytopenia	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0000598	abnormal liver morphology	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0002875	decreased erythrocyte cell number	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0003135	increased erythroid progenitor cell number	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0000689	abnormal spleen morphology	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0002083	premature death	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0002643	poikilocytosis	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0011747	myelofibrosis	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0003405	abnormal platelet shape	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0000208	decreased hematocrit	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0003405	abnormal platelet shape	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0011086	postnatal lethality, incomplete penetrance	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0002356	abnormal spleen red pulp morphology	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0006410	abnormal common myeloid progenitor cell morphology	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0011101	prenatal lethality, incomplete penetrance	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0020039	increased bone ossification	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0008801	abnormal erythroid progenitor cell morphology	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0008801	abnormal erythroid progenitor cell morphology	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0005097	polychromatophilia	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0006410	abnormal common myeloid progenitor cell morphology	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0002397	abnormal bone marrow morphology	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0000219	increased neutrophil cell number	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0009338	increased splenocyte number	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0002123	abnormal definitive hematopoiesis	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0001577	anemia	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0003179	thrombocytopenia	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0010178	increased number of Howell-Jolly bodies	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0000333	decreased bone marrow cell number	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0003135	increased erythroid progenitor cell number	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653501	F	MP:0008872	abnormal physiological response to xenobiotic	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:2653501	F	MP:0010868	increased bone trabecula number	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:2653522	F	MP:0006270	abnormal mammary gland growth during lactation	Xdh<tm1Mrc>/Xdh<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12502743
MGI:2653522	F	MP:0006271	abnormal involution of the mammary gland	Xdh<tm1Mrc>/Xdh<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12502743
MGI:2653522	F	MP:0004047	abnormal milk composition	Xdh<tm1Mrc>/Xdh<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12502743
MGI:2653522	F	MP:0001882	abnormal lactation	Xdh<tm1Mrc>/Xdh<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12502743
MGI:2653607	F	MP:0013781	abnormal mammary gland luminal epithelium morphology	Tg(BLG-STAT5A)6Itb/0	involves: FVB/N	N	12496367
MGI:2653607	F	MP:0006271	abnormal involution of the mammary gland	Tg(BLG-STAT5A)6Itb/0	involves: FVB/N	N	12496367
MGI:2653607	F	MP:0006270	abnormal mammary gland growth during lactation	Tg(BLG-STAT5A)6Itb/0	involves: FVB/N	N	12496367
MGI:2653607	F	MP:0000628	abnormal mammary gland development	Tg(BLG-STAT5A)6Itb/0	involves: FVB/N	N	12496367
MGI:2653607	F	MP:0006269	abnormal mammary gland growth during pregnancy	Tg(BLG-STAT5A)6Itb/0	involves: FVB/N	N	12496367
MGI:2653607	F	MP:0004047	abnormal milk composition	Tg(BLG-STAT5A)6Itb/0	involves: FVB/N	N	12496367
MGI:2653608	F	MP:0006269	abnormal mammary gland growth during pregnancy	Tg(BLG-STAT5A)15Itb/0	involves: FVB/N	N	12496367
MGI:2653608	F	MP:0006270	abnormal mammary gland growth during lactation	Tg(BLG-STAT5A)15Itb/0	involves: FVB/N	N	12496367
MGI:2653608	F	MP:0004047	abnormal milk composition	Tg(BLG-STAT5A)15Itb/0	involves: FVB/N	N	12496367
MGI:2653608	F	MP:0000628	abnormal mammary gland development	Tg(BLG-STAT5A)15Itb/0	involves: FVB/N	N	12496367
MGI:2653608	F	MP:0006271	abnormal involution of the mammary gland	Tg(BLG-STAT5A)15Itb/0	involves: FVB/N	N	12496367
MGI:2653608	F	MP:0010173	increased mammary gland epithelial cell proliferation	Tg(BLG-STAT5A)15Itb/0	involves: FVB/N	N	12496367
MGI:2653608	F	MP:0000627	abnormal mammary gland morphology	Tg(BLG-STAT5A)15Itb/0	involves: FVB/N	N	12496367
MGI:2653626	F	MP:0009211	absent external female genitalia	Wnt5a<tm1Amc>/Wnt5a<tm1Amc>	involves: 129S7/SvEvBrd * C57BL/6	N	10021340
MGI:2653626	M	MP:0009204	absent external male genitalia	Wnt5a<tm1Amc>/Wnt5a<tm1Amc>	involves: 129S7/SvEvBrd * C57BL/6	N	10021340
MGI:2653695	F	MP:0009017	prolonged estrus	Tnf<tm1Sek>/Tnf<tm1Sek>	involves: C57BL/6 * CBA	N	10453074
MGI:2653695	F	MP:0003699	abnormal female reproductive system physiology	Tnf<tm1Sek>/Tnf<tm1Sek>	involves: C57BL/6 * CBA	N	10639149
MGI:2653695	F	MP:0008978	abnormal vagina weight	Tnf<tm1Sek>/Tnf<tm1Sek>	involves: C57BL/6 * CBA	N	10453074
MGI:2653759	M	MP:0002675	asthenozoospermia	Vdac3<tm1Wjc>/Vdac3<tm1Wjc>	Not Specified	N	11507092
MGI:2653759	M	MP:0001925	male infertility	Vdac3<tm1Wjc>/Vdac3<tm1Wjc>	Not Specified	N	11507092
MGI:2653759	M	MP:0020451	decreased sperm progressive motility	Vdac3<tm1Wjc>/Vdac3<tm1Wjc>	Not Specified	N	11507092
MGI:2653759	M	MP:0009838	abnormal sperm axoneme morphology	Vdac3<tm1Wjc>/Vdac3<tm1Wjc>	Not Specified	N	11507092
MGI:2653844	F	MP:0001923	reduced female fertility	Abcb4<tm1Bor>/Abcb4<tm1Bor>	either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * FVB/N)	N	7977654
MGI:2653866	F	MP:0011121	decreased primordial ovarian follicle number	Amh<tm1Bhr>/Amh<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	10579345
MGI:2653866	F	MP:0004855	increased ovary weight	Amh<tm1Bhr>/Amh<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	10579345
MGI:2653866	F	MP:0031383	increased secondary ovarian follicle number	Amh<tm1Bhr>/Amh<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	10579345
MGI:2653866	F	MP:0011128	increased tertiary ovarian follicle number	Amh<tm1Bhr>/Amh<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	10579345
MGI:2653875	M	MP:0001922	reduced male fertility	Usf2<tm1Msw>/Usf2<tm1Msw>	involves: 129S7/SvEvBrd * C57BL/6	N	9520440
MGI:2653911	F	MP:0008501	increased IgG2b level	Il13ra2<tm1Gru>/Il13ra2<tm1Gru>	C.Cg-Il13ra2<tm1Gru>	N	12642602
MGI:2653911	F	MP:0008500	increased IgG2a level	Il13ra2<tm1Gru>/Il13ra2<tm1Gru>	C.Cg-Il13ra2<tm1Gru>	N	12642602
MGI:2653911	F	MP:0002398	abnormal bone marrow cell morphology/development	Il13ra2<tm1Gru>/Il13ra2<tm1Gru>	C.Cg-Il13ra2<tm1Gru>	N	12642602
MGI:2653911	F	MP:0008609	decreased circulating interleukin-13 level	Il13ra2<tm1Gru>/Il13ra2<tm1Gru>	C.Cg-Il13ra2<tm1Gru>	N	12642602
MGI:2653911	F	MP:0008660	increased interleukin-10 secretion	Il13ra2<tm1Gru>/Il13ra2<tm1Gru>	C.Cg-Il13ra2<tm1Gru>	N	12642602
MGI:2653911	F	MP:0002497	increased IgE level	Il13ra2<tm1Gru>/Il13ra2<tm1Gru>	C.Cg-Il13ra2<tm1Gru>	N	12642602
MGI:2653911	F	MP:0002495	increased IgA level	Il13ra2<tm1Gru>/Il13ra2<tm1Gru>	C.Cg-Il13ra2<tm1Gru>	N	12642602
MGI:2653911	F	MP:0008566	increased interferon-gamma secretion	Il13ra2<tm1Gru>/Il13ra2<tm1Gru>	C.Cg-Il13ra2<tm1Gru>	N	12642602
MGI:2653911	F	MP:0008734	decreased susceptibility to endotoxin shock	Il13ra2<tm1Gru>/Il13ra2<tm1Gru>	C.Cg-Il13ra2<tm1Gru>	N	12642602
MGI:2653911	F	MP:0008700	decreased interleukin-4 secretion	Il13ra2<tm1Gru>/Il13ra2<tm1Gru>	C.Cg-Il13ra2<tm1Gru>	N	12642602
MGI:2653911	F	MP:0002451	abnormal macrophage physiology	Il13ra2<tm1Gru>/Il13ra2<tm1Gru>	C.Cg-Il13ra2<tm1Gru>	N	12642602
MGI:2653911	F	MP:0008973	decreased erythroid progenitor cell number	Il13ra2<tm1Gru>/Il13ra2<tm1Gru>	C.Cg-Il13ra2<tm1Gru>	N	12642602
MGI:2653926	F	MP:0001926	female infertility	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	12629043
MGI:2653926	M	MP:0002687	oligozoospermia	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	12629043
MGI:2653926	F	MP:0001127	small ovary	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	12629043
MGI:2653926	M	MP:0002675	asthenozoospermia	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	12629043
MGI:2653926	F	MP:0005431	decreased oocyte number	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	12629043
MGI:2653926	M	MP:0005169	abnormal male meiosis	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	12629043
MGI:2653926	F	MP:0001126	abnormal ovary morphology	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	12629043
MGI:2653926	M	MP:0001147	small testis	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	12629043
MGI:2653926	M	MP:0001925	male infertility	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	12629043
MGI:2653926	M	MP:0014052	increased male germ cell apoptosis	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	12629043
MGI:2654136	F	MP:0020411	increased abdominal adipose tissue amount	Ad/Ad	involves: Chr 7 marker stock * Wild stock	N	420754
MGI:2654139	F	MP:0005620	abnormal muscle contractility	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	3440862
MGI:2654139	F	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	3239377
MGI:2654139	F	MP:0001053	abnormal neuromuscular synapse morphology	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	1686056
MGI:2654139	F	MP:0003852	skeletal muscle necrosis	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	3239377
MGI:2654139	F	MP:0004818	increased skeletal muscle mass	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	8186696
MGI:2654139	F	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	3440862
MGI:2654139	F	MP:0008874	decreased physiological sensitivity to xenobiotic	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	8047301
MGI:2654139	F	MP:0009414	skeletal muscle fiber necrosis	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	3239377
MGI:2654139	F	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	3440862
MGI:2654139	F	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	8186696
MGI:2654139	F	MP:0004089	dilated sarcoplasmic reticulum	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	3239377
MGI:2654139	F	MP:0009414	skeletal muscle fiber necrosis	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	8186696
MGI:2654139	F	MP:0004142	abnormal muscle tone	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	3209690
MGI:2654139	F	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	3209690
MGI:2654139	F	MP:0009420	skeletal muscle endomysial fibrosis	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	8186696
MGI:2654139	F	MP:0030428	abnormal scalene muscle morphology	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	1865908
MGI:2654139	F	MP:0010252	anterior subcapsular cataract	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	2250175
MGI:2654139	F	MP:0003631	nervous system phenotype	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	Y	1686056
MGI:2654139	F	MP:0004145	abnormal muscle electrophysiology	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	2250175
MGI:2654139	F	MP:0000759	abnormal skeletal muscle morphology	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	3239377
MGI:2654139	F	MP:0009401	increased skeletal muscle fiber diameter	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	3209690
MGI:2654139	F	MP:0009401	increased skeletal muscle fiber diameter	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	8186696
MGI:2654139	F	MP:0002106	abnormal muscle physiology	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	2144875
MGI:2654139	F	MP:0009414	skeletal muscle fiber necrosis	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	3440862
MGI:2654139	F	MP:0009410	abnormal skeletal muscle satellite cell proliferation	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	3239377
MGI:2654139	F	MP:0010254	nuclear cataract	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	2250175
MGI:2654139	F	MP:0002279	abnormal diaphragm morphology	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	1865908
MGI:2654139	F	MP:0009461	skeletal muscle hypertrophy	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	8186696
MGI:2654139	F	MP:0002280	abnormal intercostal muscle morphology	Dmd<mdx>/Dmd<mdx>	involves: C57BL/10ScSn	N	1865908
MGI:2654219	M	MP:0002169	no abnormal phenotype detected	Gab3<tm1Lrr>/Y	involves: 129S4/SvJae * C57BL/6	N	12640125
MGI:2654259	M	MP:0002717	abnormal male preputial gland morphology	Mab21l1<tm1Nao>/Mab21l1<tm1Nao>	involves: C57BL/6	N	12642482
MGI:2654259	M	MP:0001925	male infertility	Mab21l1<tm1Nao>/Mab21l1<tm1Nao>	involves: C57BL/6	N	12642482
MGI:2654259	M	MP:0002716	small male preputial gland	Mab21l1<tm1Nao>/Mab21l1<tm1Nao>	involves: C57BL/6	N	12642482
MGI:2654457	M	MP:0001925	male infertility	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	N	8797826
MGI:2654457	F	MP:0005389	reproductive system phenotype	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	Y	8797826
MGI:2654457	M	MP:0009831	abnormal sperm midpiece morphology	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	N	8797826
MGI:2654457	M	MP:0004852	decreased testis weight	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	N	8797826
MGI:2654457	M	MP:0001156	abnormal spermatogenesis	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	N	8797826
MGI:2654457	M	MP:0009230	abnormal sperm head morphology	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	N	8797826
MGI:2654457	M	MP:0006379	abnormal spermatocyte morphology	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	N	8797826
MGI:2654457	M	MP:0002687	oligozoospermia	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	N	8797826
MGI:2654457	M	MP:0014052	increased male germ cell apoptosis	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	N	8797826
MGI:2654457	M	MP:0002675	asthenozoospermia	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	N	8797826
MGI:2654457	M	MP:0005578	teratozoospermia	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	N	8797826
MGI:2654500	F	MP:0010249	lactation failure	Slc6a3<tm1Mca>/Slc6a3<tm1Mca>	involves: 129P2/OlaHsd	N	9247269
MGI:2654500	F	MP:0001386	abnormal maternal nurturing	Slc6a3<tm1Mca>/Slc6a3<tm1Mca>	involves: 129P2/OlaHsd	N	8628395
MGI:2654511	F	MP:0001923	reduced female fertility	Fmn2<tm1Led>/Fmn2<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	N	12447394
MGI:2654511	F	MP:0014443	impaired polar body extrusion	Fmn2<tm1Led>/Fmn2<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	N	12447394
MGI:2654511	F	MP:0012737	abnormal primary polar body morphology	Fmn2<tm1Led>/Fmn2<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	N	12447394
MGI:2654511	F	MP:0001382	abnormal nursing	Fmn2<tm1Led>/Fmn2<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	N	12447394
MGI:2654511	F	MP:0001125	abnormal oocyte morphology	Fmn2<tm1Led>/Fmn2<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	N	12447394
MGI:2654511	F	MP:0009661	abnormal pregnancy	Fmn2<tm1Led>/Fmn2<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	N	12447394
MGI:2654516	F	MP:0008054	abnormal uterine NK cell morphology	Ifngr1<tm1Agt>/Ifngr1<tm1Agt>	involves: 129S7/SvEvBrd	N	10411532
MGI:2654516	F	MP:0001120	abnormal uterus morphology	Ifngr1<tm1Agt>/Ifngr1<tm1Agt>	involves: 129S7/SvEvBrd	N	10411532
MGI:2654516	F	MP:0009099	abnormal uterine NK cell physiology	Ifngr1<tm1Agt>/Ifngr1<tm1Agt>	involves: 129S7/SvEvBrd	N	10411532
MGI:2654516	F	MP:0009394	increased uterine NK cell number	Ifngr1<tm1Agt>/Ifngr1<tm1Agt>	involves: 129S7/SvEvBrd	N	10411532
MGI:2654516	F	MP:0004256	abnormal maternal decidual layer morphology	Ifngr1<tm1Agt>/Ifngr1<tm1Agt>	involves: 129S7/SvEvBrd	N	10411532
MGI:2654574	F	MP:0009763	increased susceptibility to induced morbidity/mortality	Itgb1bp2<tm1Tron>/Itgb1bp2<tm1Tron>	involves: 129S1/Sv * 129X1/SvJ	N	12496958
MGI:2654574	F	MP:0004484	abnormal response of heart to induced stress	Itgb1bp2<tm1Tron>/Itgb1bp2<tm1Tron>	involves: 129S1/Sv * 129X1/SvJ	N	12496958
MGI:2654577	M	MP:0009763	increased susceptibility to induced morbidity/mortality	Itgb1bp2<tm1Tron>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12496958
MGI:2654577	M	MP:0004484	abnormal response of heart to induced stress	Itgb1bp2<tm1Tron>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12496958
MGI:2654708	F	MP:0004896	abnormal endometrium morphology	Lepr<db>/Lepr<db>	involves: C57BLKS/J	N	12502493
MGI:2654708	F	MP:0001120	abnormal uterus morphology	Lepr<db>/Lepr<db>	involves: C57BLKS/J	N	12502493
MGI:2654708	F	MP:0004905	decreased uterus weight	Lepr<db>/Lepr<db>	involves: C57BLKS/J	N	12502493
MGI:2654709	M	MP:0011086	postnatal lethality, incomplete penetrance	Lep<ob>/Lep<ob>	involves: C57BL/6J	N	25144618
MGI:2654710	M	MP:0006378	abnormal spermatogonia morphology	Hmga2<tm1Cha>/Hmga2<tm1Cha>	involves: 129S7/SvEvBrd	N	12032866
MGI:2654710	M	MP:0005159	azoospermia	Hmga2<tm1Cha>/Hmga2<tm1Cha>	involves: 129S7/SvEvBrd	N	12032866
MGI:2654710	M	MP:0001925	male infertility	Hmga2<tm1Cha>/Hmga2<tm1Cha>	involves: 129S7/SvEvBrd	N	12032866
MGI:2654712	F	MP:0005621	abnormal cell physiology	Dkc1<tm1Ppp>/Dkc1<+>	involves: 129S1/Sv	N	12522253
MGI:2654712	F	MP:0002060	abnormal skin morphology	Dkc1<tm1Ppp>/Dkc1<+>	involves: 129S1/Sv	N	12522253
MGI:2654712	F	MP:0000716	abnormal immune system cell morphology	Dkc1<tm1Ppp>/Dkc1<+>	involves: 129S1/Sv	N	12522253
MGI:2654712	F	MP:0002722	abnormal immune system organ morphology	Dkc1<tm1Ppp>/Dkc1<+>	involves: 129S1/Sv	N	12522253
MGI:2654712	F	MP:0000358	abnormal cell morphology	Dkc1<tm1Ppp>/Dkc1<+>	involves: 129S1/Sv	N	12522253
MGI:2654712	F	MP:0002135	abnormal kidney morphology	Dkc1<tm1Ppp>/Dkc1<+>	involves: 129S1/Sv	N	12522253
MGI:2654712	F	MP:0002020	increased tumor incidence	Dkc1<tm1Ppp>/Dkc1<+>	involves: 129S1/Sv	N	12522253
MGI:2654712	F	MP:0002447	abnormal erythrocyte morphology	Dkc1<tm1Ppp>/Dkc1<+>	involves: 129S1/Sv	N	12522253
MGI:2654712	F	MP:0001545	abnormal hematopoietic system physiology	Dkc1<tm1Ppp>/Dkc1<+>	involves: 129S1/Sv	N	12522253
MGI:2654712	F	MP:0002398	abnormal bone marrow cell morphology/development	Dkc1<tm1Ppp>/Dkc1<+>	involves: 129S1/Sv	N	12522253
MGI:2654712	F	MP:0002123	abnormal definitive hematopoiesis	Dkc1<tm1Ppp>/Dkc1<+>	involves: 129S1/Sv	N	12522253
MGI:2654712	F	MP:0001175	abnormal lung morphology	Dkc1<tm1Ppp>/Dkc1<+>	involves: 129S1/Sv	N	12522253
MGI:2654752	M	MP:0031012	impaired sperm migration in female genital tract	Adam2<tm1Dgm>/Adam2<tm1Dgm>	involves: 129P2/OlaHsd * C57BL/6N	N	9743500
MGI:2654752	M	MP:0030978	impaired binding of sperm to zona pellucida	Adam2<tm1Dgm>/Adam2<tm1Dgm>	involves: 129P2/OlaHsd * C57BL/6N	N	9743500
MGI:2654752	M	MP:0001922	reduced male fertility	Adam2<tm1Dgm>/Adam2<tm1Dgm>	involves: 129P2/OlaHsd * C57BL/6N	N	9743500
MGI:2654776	F	MP:0001382	abnormal nursing	cu/cu	involves: BALB/cGaJ	N	MGI:61656
MGI:2654780	M	MP:0009853	decreased Sertoli cell phagocytosis	Mertk<tm1Grl>/Mertk<tm1Grl>	involves: 129P2/OlaHsd	N	18159085
MGI:2654780	F	MP:0001144	vagina atresia	Mertk<tm1Grl>/Mertk<tm1Grl>	involves: 129P2/OlaHsd	N	18393392
MGI:2654781	F	MP:0009396	small endometrial glands	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18393392
MGI:2654781	F	MP:0001923	reduced female fertility	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11452127
MGI:2654781	F	MP:0001923	reduced female fertility	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10227296
MGI:2654781	F	MP:0001120	abnormal uterus morphology	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18393392
MGI:2654781	M	MP:0009853	decreased Sertoli cell phagocytosis	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18159085
MGI:2654781	F	MP:0004906	enlarged uterus	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18393392
MGI:2654781	F	MP:0013508	increased granulosa cell apoptosis	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10227296
MGI:2654781	M	MP:0001168	abnormal prostate gland epithelium morphology	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10227296
MGI:2654781	M	MP:0001147	small testis	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10227296
MGI:2654781	M	MP:0001156	abnormal spermatogenesis	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10227296
MGI:2654781	M	MP:0005159	azoospermia	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10227296
MGI:2654781	M	MP:0002216	abnormal seminiferous tubule morphology	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10227296
MGI:2654781	F	MP:0001144	vagina atresia	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18393392
MGI:2654781	M	MP:0001925	male infertility	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10227296
MGI:2654783	M	MP:0001147	small testis	Axl<tm1Grl>/Axl<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10227296
MGI:2654783	F	MP:0001938	delayed sexual maturation	Axl<tm1Grl>/Axl<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18787040
MGI:2654783	M	MP:0001156	abnormal spermatogenesis	Axl<tm1Grl>/Axl<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10227296
MGI:2654783	F	MP:0009006	prolonged estrous cycle	Axl<tm1Grl>/Axl<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18787040
MGI:2654783	F	MP:0009008	delayed estrous cycle	Axl<tm1Grl>/Axl<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18787040
MGI:2654783	F	MP:0009012	short diestrus	Axl<tm1Grl>/Axl<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18787040
MGI:2654783	F	MP:0009014	prolonged proestrus	Axl<tm1Grl>/Axl<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18787040
MGI:2654784	M	MP:0001156	abnormal spermatogenesis	Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ	N	10227296
MGI:2654784	M	MP:0002687	oligozoospermia	Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ	N	10227296
MGI:2654784	M	MP:0001147	small testis	Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ	N	10227296
MGI:2654784	F	MP:0001144	vagina atresia	Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ	N	18393392
MGI:2654784	M	MP:0009853	decreased Sertoli cell phagocytosis	Mertk<tm1Grl>/Mertk<tm1Grl>,Tyro3<tm1Grl>/Tyro3<tm1Grl>	involves: 129S1/Sv * 129X1/SvJ	N	18159085
MGI:2654823	M	MP:0003631	nervous system phenotype	Tyl/Y	involves: A/J * C57BL/6J	Y	MGI:62465
MGI:2654823	M	MP:0000745	tremors	Tyl/Y	involves: A/J * C57BL/6J	N	MGI:62465
MGI:2654823	M	MP:0002083	premature death	Tyl/Y	involves: A/J * C57BL/6J	N	MGI:62465
MGI:2654823	M	MP:0002064	seizures	Tyl/Y	involves: A/J * C57BL/6J	N	MGI:62465
MGI:2654823	M	MP:0000754	paresis	Tyl/Y	involves: A/J * C57BL/6J	N	MGI:62465
MGI:2654824	F	MP:0000745	tremors	Tyl/Tyl<+>	involves: A/J * C57BL/6J	N	MGI:62465
MGI:2654824	F	MP:0000160	kyphosis	Tyl/Tyl<+>	involves: A/J * C57BL/6J	N	MGI:62465
MGI:2654844	M	MP:0000745	tremors	Ty/Y	(129P3/J x NZB/BlNJ)F1	N	MGI:61952
MGI:2654844	M	MP:0003631	nervous system phenotype	Ty/Y	(129P3/J x NZB/BlNJ)F1	Y	MGI:61952
MGI:2654844	M	MP:0011085	postnatal lethality, complete penetrance	Ty/Y	(129P3/J x NZB/BlNJ)F1	N	MGI:61952
MGI:2654844	M	MP:0002064	seizures	Ty/Y	(129P3/J x NZB/BlNJ)F1	N	MGI:61952
MGI:2654845	F	MP:0000745	tremors	Ty/Ty<+>	(129P3/J x NZB/BlNJ)F1	N	MGI:61952
MGI:2654845	F	MP:0001405	impaired coordination	Ty/Ty<+>	(129P3/J x NZB/BlNJ)F1	N	MGI:61952
MGI:2654845	F	MP:0001926	female infertility	Ty/Ty<+>	(129P3/J x NZB/BlNJ)F1	N	MGI:61952
MGI:2654860	F	MP:0001926	female infertility	Zeb1<Tw>/Zeb1<+>	involves: C57BL/6J	N	10669096
MGI:2654860	M	MP:0001922	reduced male fertility	Zeb1<Tw>/Zeb1<+>	involves: C57BL/6J	N	10669096
MGI:2654873	F	MP:0009006	prolonged estrous cycle	Thra<tm2Ven>/Thra<tm2Ven>	involves: 129P2/OlaHsd * BALB/c	N	11731613
MGI:2654873	F	MP:0001923	reduced female fertility	Thra<tm2Ven>/Thra<tm2Ven>	involves: 129P2/OlaHsd * BALB/c	N	11731613
MGI:2654873	F	MP:0001384	abnormal pup retrieval	Thra<tm2Ven>/Thra<tm2Ven>	involves: 129P2/OlaHsd * BALB/c	N	11731613
MGI:2654874	M	MP:0005152	pancytopenia	Alas2<tm1Mym>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10562540
MGI:2654874	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Alas2<tm1Mym>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10562540
MGI:2654874	M	MP:0004229	abnormal embryonic erythropoiesis	Alas2<tm1Mym>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10562540
MGI:2654874	M	MP:0003396	abnormal embryonic hematopoiesis	Alas2<tm1Mym>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10562540
MGI:2654874	M	MP:0001577	anemia	Alas2<tm1Mym>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10562540
MGI:2654874	M	MP:0001770	abnormal iron level	Alas2<tm1Mym>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10562540
MGI:2654874	M	MP:0003717	pallor	Alas2<tm1Mym>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10562540
MGI:2654895	F	MP:0001382	abnormal nursing	alp/alp	Not Specified	N	22896273
MGI:2654933	F	MP:0001926	female infertility	Tnfaip6<tm1Cful>/Tnfaip6<tm1Cful>	involves: 129S6/SvEvTac * BALB/c	N	12668637
MGI:2654933	F	MP:0031420	decreased superovulation rate	Tnfaip6<tm1Cful>/Tnfaip6<tm1Cful>	involves: 129S6/SvEvTac * BALB/c	N	12668637
MGI:2654933	F	MP:0009374	absent cumulus expansion	Tnfaip6<tm1Cful>/Tnfaip6<tm1Cful>	involves: 129S6/SvEvTac * BALB/c	N	12668637
MGI:2654941	M	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12612578
MGI:2654941	M	MP:0005350	increased susceptibility to autoimmune disorder	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12612578
MGI:2654941	M	MP:0000020	scaly ears	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12612578
MGI:2654941	M	MP:0004947	skin inflammation	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12612578
MGI:2654941	M	MP:0008397	abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12612578
MGI:2654941	M	MP:0001192	scaly skin	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12612578
MGI:2654941	M	MP:0000691	enlarged spleen	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12612578
MGI:2654941	M	MP:0001265	decreased body size	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12612578
MGI:2654941	M	MP:0000702	enlarged lymph nodes	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12612578
MGI:2654942	F	MP:0002169	no abnormal phenotype detected	Foxp3<tm1Ayr>/Foxp3<tm1Ayr>	involves: 129S1/Sv * 129X1/SvJ	N	12612578
MGI:2655161	M	MP:0001932	abnormal spermiogenesis	Amph<tm1Pdc>/Amph<tm1Pdc>	involves: 129/Sv * C57BL/6	N	17785912
MGI:2655161	M	MP:0004182	abnormal spermiation	Amph<tm1Pdc>/Amph<tm1Pdc>	involves: 129/Sv * C57BL/6	N	17785912
MGI:2655161	M	MP:0002784	abnormal Sertoli cell morphology	Amph<tm1Pdc>/Amph<tm1Pdc>	involves: 129/Sv * C57BL/6	N	17785912
MGI:2655161	M	MP:0006380	abnormal spermatid morphology	Amph<tm1Pdc>/Amph<tm1Pdc>	involves: 129/Sv * C57BL/6	N	17785912
MGI:2655166	F	MP:0005431	decreased oocyte number	Cdk5rap2<an>/Cdk5rap2<an>	Not Specified	N	MGI:63300
MGI:2655166	M	MP:0001156	abnormal spermatogenesis	Cdk5rap2<an>/Cdk5rap2<an>	Not Specified	N	MGI:70478
MGI:2655174	M	MP:0001922	reduced male fertility	Ank<ank>/Ank<ank>	involves: C3HeB/FeJ * C57BL/6J * JGBF/LeJ	N	7276519
MGI:2655174	F	MP:0001923	reduced female fertility	Ank<ank>/Ank<ank>	involves: C3HeB/FeJ * C57BL/6J * JGBF/LeJ	N	7276519
MGI:2655194	M	MP:0008046	absent NK cells	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0000711	thymus cortex hypoplasia	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0002490	abnormal immunoglobulin level	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0001601	abnormal myelopoiesis	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0005016	decreased lymphocyte cell number	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0002416	abnormal proerythroblast morphology	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0001802	arrested B cell differentiation	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0001805	decreased IgG level	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0005018	decreased T cell number	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0000715	decreased thymocyte number	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0005046	absent spleen white pulp	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0002722	abnormal immune system organ morphology	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0000706	small thymus	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0002723	abnormal immune serum protein physiology	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0008136	enlarged Peyer's patches	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0005425	increased macrophage cell number	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0008254	increased megakaryocyte cell number	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0000219	increased neutrophil cell number	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0000220	increased monocyte cell number	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0000716	abnormal immune system cell morphology	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0001823	thymus hypoplasia	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0008826	abnormal splenic cell ratio	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0000691	enlarged spleen	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0002217	small lymph nodes	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655194	M	MP:0008498	decreased IgG3 level	Il2rg<tm1Sug>/Y	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)	N	8562967
MGI:2655216	F	MP:0013785	abnormal mammary gland bud morphology	Tbx3<tm1Pa>/Tbx3<tm1Pa>	either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac)	N	12668638
MGI:2655216	F	MP:0004135	abnormal mammary gland embryonic development	Tbx3<tm1Pa>/Tbx3<tm1Pa>	either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac)	N	12668638
MGI:2655216	F	MP:0000629	absent mammary gland	Tbx3<tm1Pa>/Tbx3<tm1Pa>	either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac)	N	12668638
MGI:2655217	F	MP:0001119	abnormal female reproductive system morphology	Tbx3<tm1Pa>/Tbx3<+>	either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac)	N	12668638
MGI:2655217	F	MP:0001142	abnormal vagina orifice morphology	Tbx3<tm1Pa>/Tbx3<+>	either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac)	N	12668638
MGI:2655217	F	MP:0003127	abnormal clitoris morphology	Tbx3<tm1Pa>/Tbx3<+>	either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac)	N	12668638
MGI:2655323	F	MP:0008523	absent lymph node germinal center	Btk<tm1Wk>/Btk<tm1Wk>,Cd40<tm1Geha>/Cd40<tm1Geha>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2655323	F	MP:0008497	decreased IgG2b level	Btk<tm1Wk>/Btk<tm1Wk>,Cd40<tm1Geha>/Cd40<tm1Geha>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2655323	F	MP:0005017	decreased B cell number	Btk<tm1Wk>/Btk<tm1Wk>,Cd40<tm1Geha>/Cd40<tm1Geha>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2655323	F	MP:0005093	decreased B cell proliferation	Btk<tm1Wk>/Btk<tm1Wk>,Cd40<tm1Geha>/Cd40<tm1Geha>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2655323	F	MP:0001806	decreased IgM level	Btk<tm1Wk>/Btk<tm1Wk>,Cd40<tm1Geha>/Cd40<tm1Geha>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2655323	F	MP:0008498	decreased IgG3 level	Btk<tm1Wk>/Btk<tm1Wk>,Cd40<tm1Geha>/Cd40<tm1Geha>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2655323	F	MP:0008474	absent spleen germinal center	Btk<tm1Wk>/Btk<tm1Wk>,Cd40<tm1Geha>/Cd40<tm1Geha>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2655323	F	MP:0001800	abnormal humoral immune response	Btk<tm1Wk>/Btk<tm1Wk>,Cd40<tm1Geha>/Cd40<tm1Geha>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2655323	F	MP:0008496	decreased IgG2a level	Btk<tm1Wk>/Btk<tm1Wk>,Cd40<tm1Geha>/Cd40<tm1Geha>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2655323	F	MP:0001807	decreased IgA level	Btk<tm1Wk>/Btk<tm1Wk>,Cd40<tm1Geha>/Cd40<tm1Geha>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2655323	F	MP:0008211	decreased mature B cell number	Btk<tm1Wk>/Btk<tm1Wk>,Cd40<tm1Geha>/Cd40<tm1Geha>	involves: 129S4/SvJae * C57BL/6	N	9088978
MGI:2655363	F	MP:0001382	abnormal nursing	ap/ap	involves: hairless stock	N	MGI:78497
MGI:2655420	M	MP:0001925	male infertility	Fmn1<ld-3J>/Fmn1<ld-3J>	NOD.Cg Prkdc<scid>/J-Fmn1<ld-3J>/GrsrJ	N	MGI:2655227
MGI:2655448	F	MP:0004263	abnormal limb posture	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0001262	decreased body weight	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0001265	decreased body size	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0001362	abnormal anxiety-related response	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0001436	abnormal suckling behavior	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0000706	small thymus	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0011086	postnatal lethality, incomplete penetrance	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0001516	abnormal motor coordination/balance	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0000745	tremors	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0000746	weakness	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0001527	athetotic walking movements	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0002108	abnormal muscle morphology	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0001513	limb grasping	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0002731	megacolon	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655448	F	MP:0000492	abnormal rectum morphology	Araf<tm1Mmc>/Araf<tm1Mmc>	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0000492	abnormal rectum morphology	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0000745	tremors	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0011086	postnatal lethality, incomplete penetrance	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0000746	weakness	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0001362	abnormal anxiety-related response	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0001265	decreased body size	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0001436	abnormal suckling behavior	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0001262	decreased body weight	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0000706	small thymus	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0001513	limb grasping	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0002108	abnormal muscle morphology	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0001527	athetotic walking movements	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0001516	abnormal motor coordination/balance	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0004263	abnormal limb posture	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655472	M	MP:0002731	megacolon	Araf<tm1Mmc>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8805280
MGI:2655486	F	MP:0008807	increased liver iron level	Heph<sla>/Heph<sla>,Hfe<tm2Nca>/Hfe<tm2Nca>	involves: 129S6/SvEvTac * C57BL/6J	N	10791995
MGI:2655486	F	MP:0020369	increased intestinal iron level	Heph<sla>/Heph<sla>,Hfe<tm2Nca>/Hfe<tm2Nca>	involves: 129S6/SvEvTac * C57BL/6J	N	10791995
MGI:2655488	M	MP:0008807	increased liver iron level	Heph<sla>/Y,Hfe<tm2Nca>/Hfe<tm2Nca>	involves: 129S6/SvEvTac * C57BL/6J	N	10791995
MGI:2655488	M	MP:0020369	increased intestinal iron level	Heph<sla>/Y,Hfe<tm2Nca>/Hfe<tm2Nca>	involves: 129S6/SvEvTac * C57BL/6J	N	10791995
MGI:2655515	F	MP:0020369	increased intestinal iron level	Heph<sla>/Heph<sla>	involves: C57BL/6J	N	10791995
MGI:2655516	F	MP:0001728	failure of embryo implantation	Bmal1<tm1Bra>/Bmal1<tm1Bra>	involves: 129	N	19056819
MGI:2655516	F	MP:0004905	decreased uterus weight	Bmal1<tm1Bra>/Bmal1<tm1Bra>	involves: 129	N	16143109
MGI:2655516	F	MP:0001926	female infertility	Bmal1<tm1Bra>/Bmal1<tm1Bra>	involves: 129	N	19056819
MGI:2655516	F	MP:0009006	prolonged estrous cycle	Bmal1<tm1Bra>/Bmal1<tm1Bra>	involves: 129	N	19056819
MGI:2655526	M	MP:0030978	impaired binding of sperm to zona pellucida	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0014052	increased male germ cell apoptosis	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0009238	coiled sperm flagellum	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0006380	abnormal spermatid morphology	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0005578	teratozoospermia	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0004852	decreased testis weight	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0009230	abnormal sperm head morphology	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0001146	abnormal testis morphology	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0002092	abnormal eye morphology	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0001922	reduced male fertility	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0000242	impaired fertilization	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0006362	abnormal male germ cell morphology	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0002687	oligozoospermia	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0002784	abnormal Sertoli cell morphology	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0005058	abnormal lysosome morphology	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0001156	abnormal spermatogenesis	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0001393	ataxia	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0009853	decreased Sertoli cell phagocytosis	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655526	M	MP:0002631	abnormal epididymis morphology	Arsa<tm1Gie>/Arsa<tm1Gie>	involves: 129P2/OlaHsd * C57BL/6J	N	21965315
MGI:2655555	M	MP:0001146	abnormal testis morphology	Asb1<tm1Wehi>/Asb1<tm1Wehi>	involves: C57BL/6	N	11509662
MGI:2655555	M	MP:0001156	abnormal spermatogenesis	Asb1<tm1Wehi>/Asb1<tm1Wehi>	involves: C57BL/6	N	11509662
MGI:2655584	M	MP:0001147	small testis	at/at	involves: DBA/1oHu	N	MGI:61636
MGI:2655584	F	MP:0001127	small ovary	at/at	involves: DBA/1oHu	N	MGI:61636
MGI:2655584	M	MP:0004901	decreased male germ cell number	at/at	involves: DBA/1oHu	N	476239
MGI:2655584	M	MP:0002216	abnormal seminiferous tubule morphology	at/at	involves: DBA/1oHu	N	476239
MGI:2655584	M	MP:0001925	male infertility	at/at	involves: DBA/1oHu	N	MGI:61636
MGI:2655584	M	MP:0004901	decreased male germ cell number	at/at	involves: DBA/1oHu	N	MGI:61636
MGI:2655584	F	MP:0001926	female infertility	at/at	involves: DBA/1oHu	N	MGI:61636
MGI:2655584	F	MP:0005431	decreased oocyte number	at/at	involves: DBA/1oHu	N	MGI:61636
MGI:2655588	F	MP:0001935	decreased litter size	Tpst1<tm1Klm>/Tpst1<tm1Klm>	129S-Tpst1<tm1Klm>	N	11964405
MGI:2655588	F	MP:0001386	abnormal maternal nurturing	Tpst1<tm1Klm>/Tpst1<tm1Klm>	129S-Tpst1<tm1Klm>	N	11964405
MGI:2655588	F	MP:0001923	reduced female fertility	Tpst1<tm1Klm>/Tpst1<tm1Klm>	129S-Tpst1<tm1Klm>	N	11964405
MGI:2655622	M	MP:0005169	abnormal male meiosis	Top3b<tm1Jcw>/Top3b<tm1Jcw>	involves: 129S6/SvEvTac * C57BL/6	N	12591952
MGI:2655622	F	MP:0001923	reduced female fertility	Top3b<tm1Jcw>/Top3b<tm1Jcw>	involves: 129S6/SvEvTac * C57BL/6	N	12591952
MGI:2655624	M	MP:0011941	increased fluid intake	Agtr2<tm1Gsb>/Y	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	12388241
MGI:2655624	M	MP:0011947	abnormal fluid intake	Agtr2<tm1Gsb>/Y	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	7477266
MGI:2655624	M	MP:0001402	decreased locomotor activity	Agtr2<tm1Gsb>/Y	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	7477266
MGI:2655624	M	MP:0000230	abnormal systemic arterial blood pressure	Agtr2<tm1Gsb>/Y	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	7477266
MGI:2655624	M	MP:0006144	increased systemic arterial systolic blood pressure	Agtr2<tm1Gsb>/Y	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	12388241
MGI:2655634	M	MP:0011490	ureteropelvic junction stenosis	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0011492	ureterovesical junction obstruction	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0011493	double ureter	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0011489	ureteropelvic junction atresia	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0009109	decreased pancreas weight	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19033539
MGI:2655634	M	MP:0011415	abnormal aldosterone level	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12218346
MGI:2655634	M	MP:0003672	abnormal ureter development	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0003918	decreased kidney weight	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:2655634	M	MP:0001748	increased circulating adrenocorticotropin level	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12218346
MGI:2655634	M	MP:0001489	decreased startle reflex	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	7477267
MGI:2655634	M	MP:0002842	increased systemic arterial blood pressure	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	7477267
MGI:2655634	M	MP:0001745	increased circulating corticosterone level	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12218346
MGI:2655634	M	MP:0008873	increased physiological sensitivity to xenobiotic	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19033539
MGI:2655634	M	MP:0003043	hypoalgesia	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	7477267
MGI:2655634	M	MP:0003638	abnormal response/metabolism to endogenous compounds	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:2655634	M	MP:0009150	pancreatic acinar cell atrophy	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19033539
MGI:2655634	M	MP:0003963	abnormal corticosterone level	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12218346
MGI:2655634	M	MP:0002834	decreased heart weight	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:2655634	M	MP:0000536	hydroureter	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0000520	absent kidney	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0000534	abnormal ureter morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0000519	hydronephrosis	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0012575	increased noradrenaline level	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12218346
MGI:2655634	M	MP:0010867	abnormal bone trabecula morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19004830
MGI:2655634	M	MP:0010868	increased bone trabecula number	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19004830
MGI:2655634	M	MP:0010875	increased bone volume	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19004830
MGI:2655634	M	MP:0000527	abnormal kidney development	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0003585	large ureter	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0001629	abnormal heart rate	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:2655634	M	MP:0010932	increased trabecular bone connectivity density	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19004830
MGI:2655634	M	MP:0003600	ectopic kidney	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0000516	abnormal renal/urinary system morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0008528	polycystic kidney	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0004875	increased mean systemic arterial blood pressure	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:2655634	M	MP:0003334	pancreas fibrosis	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19033539
MGI:2655634	M	MP:0003459	increased fear-related response	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	7477267
MGI:2655634	M	MP:0009347	increased trabecular bone thickness	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19004830
MGI:2655634	M	MP:0001417	decreased exploration in new environment	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	7477267
MGI:2655634	M	MP:0005534	decreased body temperature	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	7477267
MGI:2655634	M	MP:0030761	increased adrenaline level	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12218346
MGI:2655634	M	MP:0003446	renal hypoplasia	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0005502	abnormal renal/urinary system physiology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0006144	increased systemic arterial systolic blood pressure	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	7477267
MGI:2655634	M	MP:0006143	increased systemic arterial diastolic blood pressure	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	7477267
MGI:2655634	M	MP:0002135	abnormal kidney morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:2655634	M	MP:0001944	abnormal pancreas morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19033539
MGI:2655642	M	MP:0005598	decreased heart ventricle muscle contractility	Atp2a2<tm1Ges>/Atp2a2<+>	involves: 129X1/SvJ * Black Swiss	N	9891028
MGI:2655642	M	MP:0003822	decreased left ventricle systolic pressure	Atp2a2<tm1Ges>/Atp2a2<+>	involves: 129X1/SvJ * Black Swiss	N	9891028
MGI:2655642	M	MP:0004084	abnormal cardiac muscle relaxation	Atp2a2<tm1Ges>/Atp2a2<+>	involves: 129X1/SvJ * Black Swiss	N	9891028
MGI:2655642	M	MP:0009105	penis prolapse	Atp2a2<tm1Ges>/Atp2a2<+>	involves: 129X1/SvJ * Black Swiss	N	11389134
MGI:2655650	F	MP:0001923	reduced female fertility	Tns1<tm1Efu>/Tns1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9087448
MGI:2655702	F	MP:0001386	abnormal maternal nurturing	Ap3b1<pe>/Ap3b1<pe>	involves: C3H/He	N	MGI:63458
MGI:2655702	F	MP:0001926	female infertility	Ap3b1<pe>/Ap3b1<pe>	involves: C3H/He	N	MGI:63458
MGI:2655816	M	MP:0004852	decreased testis weight	Pafah1b2<tm1Arai>/Pafah1b2<tm1Arai>	involves: 129X1/SvJ * C57BL/6N	N	12551946
MGI:2655820	M	MP:0014052	increased male germ cell apoptosis	Pafah1b2<tm1Arai>/Pafah1b2<tm1Arai>,Pafah1b3<tm1Arai>/Pafah1b3<tm1Arai>	involves: 129X1/SvJ * C57BL/6N	N	12551946
MGI:2655820	M	MP:0001147	small testis	Pafah1b2<tm1Arai>/Pafah1b2<tm1Arai>,Pafah1b3<tm1Arai>/Pafah1b3<tm1Arai>	involves: 129X1/SvJ * C57BL/6N	N	12551946
MGI:2655820	M	MP:0006362	abnormal male germ cell morphology	Pafah1b2<tm1Arai>/Pafah1b2<tm1Arai>,Pafah1b3<tm1Arai>/Pafah1b3<tm1Arai>	involves: 129X1/SvJ * C57BL/6N	N	12551946
MGI:2655820	M	MP:0006380	abnormal spermatid morphology	Pafah1b2<tm1Arai>/Pafah1b2<tm1Arai>,Pafah1b3<tm1Arai>/Pafah1b3<tm1Arai>	involves: 129X1/SvJ * C57BL/6N	N	12551946
MGI:2655820	M	MP:0004901	decreased male germ cell number	Pafah1b2<tm1Arai>/Pafah1b2<tm1Arai>,Pafah1b3<tm1Arai>/Pafah1b3<tm1Arai>	involves: 129X1/SvJ * C57BL/6N	N	12551946
MGI:2655820	M	MP:0001153	small seminiferous tubules	Pafah1b2<tm1Arai>/Pafah1b2<tm1Arai>,Pafah1b3<tm1Arai>/Pafah1b3<tm1Arai>	involves: 129X1/SvJ * C57BL/6N	N	12551946
MGI:2655820	M	MP:0001925	male infertility	Pafah1b2<tm1Arai>/Pafah1b2<tm1Arai>,Pafah1b3<tm1Arai>/Pafah1b3<tm1Arai>	involves: 129X1/SvJ * C57BL/6N	N	12551946
MGI:2655820	M	MP:0004852	decreased testis weight	Pafah1b2<tm1Arai>/Pafah1b2<tm1Arai>,Pafah1b3<tm1Arai>/Pafah1b3<tm1Arai>	involves: 129X1/SvJ * C57BL/6N	N	12551946
MGI:2655820	M	MP:0001156	abnormal spermatogenesis	Pafah1b2<tm1Arai>/Pafah1b2<tm1Arai>,Pafah1b3<tm1Arai>/Pafah1b3<tm1Arai>	involves: 129X1/SvJ * C57BL/6N	N	12551946
MGI:2655820	M	MP:0005159	azoospermia	Pafah1b2<tm1Arai>/Pafah1b2<tm1Arai>,Pafah1b3<tm1Arai>/Pafah1b3<tm1Arai>	involves: 129X1/SvJ * C57BL/6N	N	12551946
MGI:2655964	M	MP:0009232	abnormal sperm nucleus morphology	Tnp1<tm1Mlm>/Tnp1<tm1Mlm>	involves: 129S7/SvEvBrd * C57BL/6J	N	10781074
MGI:2655964	M	MP:0001922	reduced male fertility	Tnp1<tm1Mlm>/Tnp1<tm1Mlm>	involves: 129S7/SvEvBrd * C57BL/6J	N	10781074
MGI:2655964	M	MP:0006380	abnormal spermatid morphology	Tnp1<tm1Mlm>/Tnp1<tm1Mlm>	involves: 129S7/SvEvBrd * C57BL/6J	N	10781074
MGI:2655964	M	MP:0002675	asthenozoospermia	Tnp1<tm1Mlm>/Tnp1<tm1Mlm>	involves: 129S7/SvEvBrd * C57BL/6J	N	10781074
MGI:2655964	M	MP:0001932	abnormal spermiogenesis	Tnp1<tm1Mlm>/Tnp1<tm1Mlm>	involves: 129S7/SvEvBrd * C57BL/6J	N	10781074
MGI:2655964	M	MP:0001925	male infertility	Tnp1<tm1Mlm>/Tnp1<tm1Mlm>	involves: 129S7/SvEvBrd * C57BL/6J	N	10781074
MGI:2655964	M	MP:0009238	coiled sperm flagellum	Tnp1<tm1Mlm>/Tnp1<tm1Mlm>	involves: 129S7/SvEvBrd * C57BL/6J	N	10781074
MGI:2655990	F	MP:0001728	failure of embryo implantation	B3galnt1<tm1Led>/B3galnt1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	11463849
MGI:2656014	F	MP:0001144	vagina atresia	Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	N	11163212
MGI:2656214	F	MP:0001923	reduced female fertility	Bda/Bda	Not Specified	N	MGI:62157
MGI:2656232	M	MP:0001925	male infertility	Herc2<jdf2-3R>/Herc2<jdf2-3R>	Not Specified	N	MGI:3588414
MGI:2656232	F	MP:0001926	female infertility	Herc2<jdf2-3R>/Herc2<jdf2-3R>	Not Specified	N	MGI:3588414
MGI:2656632	F	MP:0011186	abnormal visceral endoderm morphology	Amot<tm1Bhr>/Amot<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	12676095
MGI:2656632	F	MP:0003984	embryonic growth retardation	Amot<tm1Bhr>/Amot<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	12676095
MGI:2656632	F	MP:0002084	abnormal developmental patterning	Amot<tm1Bhr>/Amot<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	12676095
MGI:2656632	F	MP:0001914	hemorrhage	Amot<tm1Bhr>/Amot<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	12676095
MGI:2656632	F	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance	Amot<tm1Bhr>/Amot<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	12676095
MGI:2656632	F	MP:0011255	abnormal anterior visceral endoderm cell migration	Amot<tm1Bhr>/Amot<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	12676095
MGI:2656633	M	MP:0002084	abnormal developmental patterning	Amot<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	12676095
MGI:2656633	M	MP:0011186	abnormal visceral endoderm morphology	Amot<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	12676095
MGI:2656633	M	MP:0001914	hemorrhage	Amot<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	12676095
MGI:2656633	M	MP:0011255	abnormal anterior visceral endoderm cell migration	Amot<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	12676095
MGI:2656633	M	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance	Amot<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	12676095
MGI:2656633	M	MP:0003984	embryonic growth retardation	Amot<tm1Bhr>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	12676095
MGI:2656637	F	MP:0001926	female infertility	Cebpb<tm1Kish>/Cebpb<tm1Kish>	involves: 129P2/OlaHsd	N	9405372
MGI:2656640	M	MP:0001394	circling	Pou3f4<del-J>/Y	C3HeB/FeJ-Pou3f4<del-J>/J	N	MGI:2656594
MGI:2656640	M	MP:0001410	head bobbing	Pou3f4<del-J>/Y	C3HeB/FeJ-Pou3f4<del-J>/J	N	MGI:2656594
MGI:2656640	M	MP:0001410	head bobbing	Pou3f4<del-J>/Y	C3HeB/FeJ-Pou3f4<del-J>/J	N	16235133
MGI:2656640	M	MP:0006325	impaired hearing	Pou3f4<del-J>/Y	C3HeB/FeJ-Pou3f4<del-J>/J	N	MGI:2656594
MGI:2656640	M	MP:0004813	absent linear vestibular evoked potential	Pou3f4<del-J>/Y	C3HeB/FeJ-Pou3f4<del-J>/J	N	16235133
MGI:2656641	F	MP:0001394	circling	Pou3f4<del-J>/Pou3f4<del-J>	C3HeB/FeJ-Pou3f4<del-J>/J	N	MGI:2656594
MGI:2656641	F	MP:0001410	head bobbing	Pou3f4<del-J>/Pou3f4<del-J>	C3HeB/FeJ-Pou3f4<del-J>/J	N	MGI:2656594
MGI:2656641	F	MP:0006325	impaired hearing	Pou3f4<del-J>/Pou3f4<del-J>	C3HeB/FeJ-Pou3f4<del-J>/J	N	MGI:2656594
MGI:2656641	F	MP:0004813	absent linear vestibular evoked potential	Pou3f4<del-J>/Pou3f4<del-J>	C3HeB/FeJ-Pou3f4<del-J>/J	N	16235133
MGI:2656641	F	MP:0001410	head bobbing	Pou3f4<del-J>/Pou3f4<del-J>	C3HeB/FeJ-Pou3f4<del-J>/J	N	16235133
MGI:2656730	F	MP:0001885	mammary gland duct hyperplasia	Tg(CMV-GAL4)1Shy/0,Tg(Pgr)2Shy/0	Not Specified	N	9435255
MGI:2656730	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(CMV-GAL4)1Shy/0,Tg(Pgr)2Shy/0	Not Specified	N	9435255
MGI:2656730	F	MP:0009503	abnormal mammary gland duct morphology	Tg(CMV-GAL4)1Shy/0,Tg(Pgr)2Shy/0	Not Specified	N	9435255
MGI:2656744	F	MP:0001729	impaired embryo implantation	Mrc1<tm1Jub>/Mrc1<+>	involves: 129X1/SvJ * C57BL/6J	N	11805139
MGI:2656746	M	MP:0009380	abnormal prostate gland ventral lobe morphology	Hoxb13<tm2Mrc>/Hoxb13<tm2Mrc>	Not Specified	N	12668621
MGI:2656748	M	MP:0009380	abnormal prostate gland ventral lobe morphology	Hoxb13<tm1Mrc>/Hoxb13<tm1Mrc>	Not Specified	N	12668621
MGI:2656748	M	MP:0003607	abnormal prostate gland physiology	Hoxb13<tm1Mrc>/Hoxb13<tm1Mrc>	Not Specified	N	12668621
MGI:2656751	M	MP:0009380	abnormal prostate gland ventral lobe morphology	Hoxb13<tm1Mrc>/Hoxb13<tm1Mrc>,Hoxd13<tm1Mrc>/Hoxd13<tm1Mrc>	involves: 129S7/SvEvBrd	N	12668621
MGI:2656752	M	MP:0009380	abnormal prostate gland ventral lobe morphology	Hoxb13<tm2Mrc>/Hoxb13<tm2Mrc>,Hoxd13<tm1Mrc>/Hoxd13<tm1Mrc>	involves: 129S7/SvEvBrd	N	12668621
MGI:2656913	M	MP:0001922	reduced male fertility	Selenop<tm1Rfb>/Selenop<tm1Rfb>	involves: 129 * C57BL/6J	N	12574155
MGI:2657150	F	MP:0031420	decreased superovulation rate	Nrip1<tm1Mpk>/Nrip1<tm1Mpk>	involves: 129/Ola	N	11100122
MGI:2657150	F	MP:0009648	abnormal superovulation	Nrip1<tm1Mpk>/Nrip1<tm1Mpk>	involves: 129/Ola	N	11100122
MGI:2657150	F	MP:0001926	female infertility	Nrip1<tm1Mpk>/Nrip1<tm1Mpk>	involves: 129/Ola	N	11100122
MGI:2657150	F	MP:0001125	abnormal oocyte morphology	Nrip1<tm1Mpk>/Nrip1<tm1Mpk>	involves: 129/Ola	N	11100122
MGI:2657150	F	MP:0008869	anovulation	Nrip1<tm1Mpk>/Nrip1<tm1Mpk>	involves: 129/Ola	N	11100122
MGI:2657189	M	MP:0001922	reduced male fertility	Cux1<tm2Ejn>/Cux1<tm2Ejn>	involves: 129S4/SvJae * C57BL/6	N	11839809
MGI:2657220	F	MP:0001928	abnormal ovulation	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas	N	8945475
MGI:2657220	M	MP:0004852	decreased testis weight	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas	N	8945475
MGI:2657220	M	MP:0002687	oligozoospermia	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas	N	8945475
MGI:2657220	F	MP:0001130	abnormal ovarian folliculogenesis	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas	N	8945475
MGI:2657220	F	MP:0001926	female infertility	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas	N	8945475
MGI:2657222	F	MP:0000628	abnormal mammary gland development	Tg(CMV-GAL4)1Shy/0,Tg(Pgr)3Shy/0	Not Specified	N	10737785
MGI:2657236	M	MP:0001156	abnormal spermatogenesis	Utp14b<jsd>/Utp14b<jsd>	involves: C57BL/6J	N	1346141
MGI:2657236	M	MP:0001940	testis hypoplasia	Utp14b<jsd>/Utp14b<jsd>	involves: C57BL/6J	N	3401545
MGI:2657236	M	MP:0004852	decreased testis weight	Utp14b<jsd>/Utp14b<jsd>	involves: C57BL/6J	N	3401545
MGI:2657236	M	MP:0001156	abnormal spermatogenesis	Utp14b<jsd>/Utp14b<jsd>	involves: C57BL/6J	N	3401545
MGI:2657243	M	MP:0001155	arrest of spermatogenesis	Ccna1<tm1Djw>/Ccna1<tm1Djw>	involves: 129S7/SvEvBrd	N	9843212
MGI:2657243	M	MP:0008261	arrest of male meiosis	Ccna1<tm1Djw>/Ccna1<tm1Djw>	involves: 129S7/SvEvBrd	N	9843212
MGI:2657243	M	MP:0020550	multinucleated giant male germ cells	Ccna1<tm1Djw>/Ccna1<tm1Djw>	involves: 129S7/SvEvBrd	N	9843212
MGI:2657243	M	MP:0014052	increased male germ cell apoptosis	Ccna1<tm1Djw>/Ccna1<tm1Djw>	involves: 129S7/SvEvBrd	N	9843212
MGI:2657243	M	MP:0001925	male infertility	Ccna1<tm1Djw>/Ccna1<tm1Djw>	involves: 129S7/SvEvBrd	N	9843212
MGI:2657243	M	MP:0004852	decreased testis weight	Ccna1<tm1Djw>/Ccna1<tm1Djw>	involves: 129S7/SvEvBrd	N	9843212
MGI:2657256	M	MP:0000135	decreased compact bone thickness	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	9731537
MGI:2657256	M	MP:0000130	abnormal trabecular bone morphology	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	9731537
MGI:2657256	M	MP:0000131	abnormal long bone epiphysis morphology	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	9731537
MGI:2657256	M	MP:0004214	abnormal long bone diaphysis morphology	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	9731537
MGI:2657256	M	MP:0011643	abnormal tendon collagen fibril morphology	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	11978731
MGI:2657256	M	MP:0000559	abnormal femur morphology	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	9731537
MGI:2657256	M	MP:0001262	decreased body weight	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	9731537
MGI:2657256	M	MP:0004989	decreased osteoblast cell number	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	9731537
MGI:2657256	M	MP:0003560	osteoarthritis	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	11978731
MGI:2657256	M	MP:0000066	osteoporosis	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	9731537
MGI:2657256	M	MP:0003109	short femur	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	9731537
MGI:2657256	M	MP:0000133	abnormal long bone metaphysis morphology	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	9731537
MGI:2657256	M	MP:0010124	decreased bone mineral content	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	9731537
MGI:2657256	M	MP:0008271	abnormal bone ossification	Bgn<tm1Mfy>/Y	involves: 129S4/SvJae * C57BL/6	N	11978731
MGI:2657263	M	MP:0000346	broad head	Bhd/Y	Not Specified	N	MGI:61920
MGI:2657263	M	MP:0002082	postnatal lethality	Bhd/Y	Not Specified	N	MGI:61920
MGI:2657263	M	MP:0030189	broad snout	Bhd/Y	Not Specified	N	MGI:61920
MGI:2657266	F	MP:0000346	broad head	Bhd/Bhd<+>	Not Specified	N	MGI:61920
MGI:2657266	F	MP:0010768	mortality/aging	Bhd/Bhd<+>	Not Specified	Y	MGI:61920
MGI:2657266	F	MP:0030189	broad snout	Bhd/Bhd<+>	Not Specified	N	MGI:61920
MGI:2657281	F	MP:0000592	short tail	Zic3<Bn>/Zic3<+>	BNT/LeJ	N	10861288
MGI:2657281	F	MP:0001539	decreased caudal vertebrae number	Zic3<Bn>/Zic3<+>	BNT/LeJ	N	10861288
MGI:2657281	F	MP:0000592	short tail	Zic3<Bn>/Zic3<+>	BNT/LeJ	N	MGI:63130
MGI:2657281	F	MP:0000592	short tail	Zic3<Bn>/Zic3<+>	BNT/LeJ	N	16589192
MGI:2657281	F	MP:0000585	kinked tail	Zic3<Bn>/Zic3<+>	BNT/LeJ	N	16589192
MGI:2657281	F	MP:0000585	kinked tail	Zic3<Bn>/Zic3<+>	BNT/LeJ	N	MGI:63130
MGI:2657281	F	MP:0002767	situs ambiguus	Zic3<Bn>/Zic3<+>	BNT/LeJ	N	10942421
MGI:2657281	F	MP:0000585	kinked tail	Zic3<Bn>/Zic3<+>	BNT/LeJ	N	10861288
MGI:2657283	F	MP:0000441	increased cranium width	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	1018005
MGI:2657283	F	MP:0000592	short tail	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	16589192
MGI:2657283	F	MP:0000592	short tail	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	MGI:63130
MGI:2657283	F	MP:0000592	short tail	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	10942421
MGI:2657283	F	MP:0000592	short tail	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	10861288
MGI:2657283	F	MP:0002767	situs ambiguus	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	10942421
MGI:2657283	F	MP:0000919	cranioschisis	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	10861288
MGI:2657283	F	MP:0002083	premature death	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	16589192
MGI:2657283	F	MP:0011101	prenatal lethality, incomplete penetrance	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	10861288
MGI:2657283	F	MP:0000914	exencephaly	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	10861288
MGI:2657283	F	MP:0001539	decreased caudal vertebrae number	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	10861288
MGI:2657283	F	MP:0001921	reduced fertility	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	16589192
MGI:2657283	F	MP:0001921	reduced fertility	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	MGI:63130
MGI:2657283	F	MP:0001921	reduced fertility	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	10861288
MGI:2657283	F	MP:0002083	premature death	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	MGI:63130
MGI:2657283	F	MP:0000074	abnormal neurocranium morphology	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	1018005
MGI:2657283	F	MP:0000919	cranioschisis	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	1018005
MGI:2657283	F	MP:0000585	kinked tail	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	16589192
MGI:2657283	F	MP:0000585	kinked tail	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	MGI:63130
MGI:2657283	F	MP:0000585	kinked tail	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	10942421
MGI:2657283	F	MP:0000585	kinked tail	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	10861288
MGI:2657283	F	MP:0000914	exencephaly	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	1018005
MGI:2657283	F	MP:0000929	open neural tube	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	10861288
MGI:2657283	F	MP:0001732	postnatal growth retardation	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	10861288
MGI:2657283	F	MP:0000929	open neural tube	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	1018005
MGI:2657283	F	MP:0008818	abnormal interfrontal bone morphology	Zic3<Bn>/Zic3<Bn>	BNT/LeJ	N	1018005
MGI:2657303	F	MP:0001727	abnormal embryo implantation	Bld/Bld	involves: BALB/cCi	N	448262
MGI:2658680	F	MP:0001926	female infertility	Egr1<tm1Jmi>/Egr1<tm1Jmi>	involves: 129	N	8703054
MGI:2658680	F	MP:0001928	abnormal ovulation	Egr1<tm1Jmi>/Egr1<tm1Jmi>	involves: 129	N	8703054
MGI:2658680	F	MP:0009009	absent estrous cycle	Egr1<tm1Jmi>/Egr1<tm1Jmi>	involves: 129	N	8703054
MGI:2658680	F	MP:0004905	decreased uterus weight	Egr1<tm1Jmi>/Egr1<tm1Jmi>	involves: 129	N	8703054
MGI:2658680	F	MP:0001134	absent corpus luteum	Egr1<tm1Jmi>/Egr1<tm1Jmi>	involves: 129	N	8703054
MGI:2658680	F	MP:0001126	abnormal ovary morphology	Egr1<tm1Jmi>/Egr1<tm1Jmi>	involves: 129	N	8703054
MGI:2658680	M	MP:0013599	Leydig cell atrophy	Egr1<tm1Jmi>/Egr1<tm1Jmi>	involves: 129	N	8703054
MGI:2658717	F	MP:0008869	anovulation	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658717	F	MP:0002637	small uterus	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658717	M	MP:0002774	small prostate gland	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658717	M	MP:0001153	small seminiferous tubules	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658717	F	MP:0001926	female infertility	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658717	M	MP:0004852	decreased testis weight	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658717	M	MP:0002687	oligozoospermia	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658717	F	MP:0004896	abnormal endometrium morphology	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658717	M	MP:0002566	abnormal sexual interaction	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658717	F	MP:0001132	absent mature ovarian follicles	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658717	F	MP:0001134	absent corpus luteum	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658717	M	MP:0001925	male infertility	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658717	M	MP:0005536	decreased Leydig cell number	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658717	M	MP:0001157	small seminal vesicle	Egr1<tm1Pch>/Egr1<tm1Pch>	involves: 129S2/SvPas * C57BL/6J	N	9440815
MGI:2658746	M	MP:0001156	abnormal spermatogenesis	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0008892	abnormal sperm flagellum morphology	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0001153	small seminiferous tubules	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0009230	abnormal sperm head morphology	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0001147	small testis	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0009237	kinked sperm flagellum	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0014052	increased male germ cell apoptosis	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0002687	oligozoospermia	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0005169	abnormal male meiosis	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0001152	increased Leydig cell number	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0004852	decreased testis weight	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0005578	teratozoospermia	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0004901	decreased male germ cell number	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0002216	abnormal seminiferous tubule morphology	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0009238	coiled sperm flagellum	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0001925	male infertility	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658746	M	MP:0008893	detached sperm flagellum	Egr4<tm1Jmi>/Egr4<tm1Jmi>	involves: C57BL/6	N	10529423
MGI:2658811	F	MP:0000008	increased white adipose tissue amount	Brs3<tm1Hoh>/Brs3<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	N	9367152
MGI:2658811	F	MP:0001433	polyphagia	Brs3<tm1Hoh>/Brs3<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	N	9367152
MGI:2658811	F	MP:0002078	abnormal glucose homeostasis	Brs3<tm1Hoh>/Brs3<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	N	9367152
MGI:2658811	F	MP:0002842	increased systemic arterial blood pressure	Brs3<tm1Hoh>/Brs3<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	N	9367152
MGI:2658811	F	MP:0011942	decreased fluid intake	Brs3<tm1Hoh>/Brs3<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	N	9367152
MGI:2658811	F	MP:0014441	decreased response to leptin	Brs3<tm1Hoh>/Brs3<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	N	9367152
MGI:2658811	F	MP:0002079	increased circulating insulin level	Brs3<tm1Hoh>/Brs3<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	N	9367152
MGI:2658811	F	MP:0001261	obese	Brs3<tm1Hoh>/Brs3<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	N	9367152
MGI:2658811	F	MP:0005669	increased circulating leptin level	Brs3<tm1Hoh>/Brs3<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	N	9367152
MGI:2658811	F	MP:0005376	homeostasis/metabolism phenotype	Brs3<tm1Hoh>/Brs3<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	Y	9367152
MGI:2658811	F	MP:0005290	decreased oxygen consumption	Brs3<tm1Hoh>/Brs3<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	N	9367152
MGI:2658811	F	MP:0005386	behavior/neurological phenotype	Brs3<tm1Hoh>/Brs3<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	Y	9367152
MGI:2658811	F	MP:0005120	decreased circulating growth hormone level	Brs3<tm1Hoh>/Brs3<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	N	9367152
MGI:2658839	M	MP:0020869	immotile sperm	Tbc1d20<bs>/Tbc1d20<bs>	involves: AKR/J	N	3955134
MGI:2658839	M	MP:0009230	abnormal sperm head morphology	Tbc1d20<bs>/Tbc1d20<bs>	involves: AKR/J	N	3955134
MGI:2658839	M	MP:0002687	oligozoospermia	Tbc1d20<bs>/Tbc1d20<bs>	involves: AKR/J	N	3955134
MGI:2658839	M	MP:0001932	abnormal spermiogenesis	Tbc1d20<bs>/Tbc1d20<bs>	involves: AKR/J	N	3955134
MGI:2658839	M	MP:0001925	male infertility	Tbc1d20<bs>/Tbc1d20<bs>	involves: AKR/J	N	3955134
MGI:2658839	M	MP:0001925	male infertility	Tbc1d20<bs>/Tbc1d20<bs>	involves: AKR/J	N	6863898
MGI:2658839	M	MP:0001155	arrest of spermatogenesis	Tbc1d20<bs>/Tbc1d20<bs>	involves: AKR/J	N	6863898
MGI:2658839	M	MP:0005578	teratozoospermia	Tbc1d20<bs>/Tbc1d20<bs>	involves: AKR/J	N	3955134
MGI:2658839	M	MP:0004852	decreased testis weight	Tbc1d20<bs>/Tbc1d20<bs>	involves: AKR/J	N	3955134
MGI:2658839	M	MP:0006362	abnormal male germ cell morphology	Tbc1d20<bs>/Tbc1d20<bs>	involves: AKR/J	N	3955134
MGI:2658839	M	MP:0001147	small testis	Tbc1d20<bs>/Tbc1d20<bs>	involves: AKR/J	N	3955134
MGI:2658839	M	MP:0008839	absent acrosome	Tbc1d20<bs>/Tbc1d20<bs>	involves: AKR/J	N	3955134
MGI:2658839	M	MP:0002687	oligozoospermia	Tbc1d20<bs>/Tbc1d20<bs>	involves: AKR/J	N	6863898
MGI:2658861	F	MP:0003356	impaired luteinization	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658861	F	MP:0001126	abnormal ovary morphology	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658861	F	MP:0008257	thin myometrium	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658861	F	MP:0013507	increased ovary apoptosis	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658861	F	MP:0001926	female infertility	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11241177
MGI:2658861	F	MP:0031422	failure of superovulation	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658861	F	MP:0008258	thin endometrium	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658861	F	MP:0001926	female infertility	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658861	M	MP:0001922	reduced male fertility	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11241177
MGI:2658861	F	MP:0002777	absent ovarian follicles	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658861	F	MP:0002637	small uterus	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658861	M	MP:0002566	abnormal sexual interaction	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11241177
MGI:2658861	F	MP:0001134	absent corpus luteum	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658861	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11241177
MGI:2658861	F	MP:0004905	decreased uterus weight	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658861	F	MP:0004905	decreased uterus weight	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11162635
MGI:2658861	M	MP:0004909	increased seminal vesicle weight	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11162635
MGI:2658861	F	MP:0008869	anovulation	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658861	F	MP:0002016	ovary cyst	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658861	F	MP:0004834	ovary hemorrhage	Cyp19a1<tm1Toda>/Cyp19a1<tm1Toda>	involves: 129P2/OlaHsd * C57BL/6J	N	11431142
MGI:2658880	M	MP:0001380	reduced male mating frequency	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	9826549
MGI:2658880	F	MP:0001926	female infertility	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	9826549
MGI:2658880	F	MP:0004771	increased anti-single stranded DNA antibody level	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	25447050
MGI:2658880	F	MP:0003725	increased autoantibody level	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	25447050
MGI:2658880	F	MP:0020411	increased abdominal adipose tissue amount	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	25447050
MGI:2658880	F	MP:0008880	lacrimal gland inflammation	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	25447050
MGI:2658880	M	MP:0001922	reduced male fertility	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	9826549
MGI:2658880	F	MP:0005350	increased susceptibility to autoimmune disorder	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	25447050
MGI:2658880	F	MP:0001134	absent corpus luteum	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	9826549
MGI:2658880	F	MP:0005425	increased macrophage cell number	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	25447050
MGI:2658880	F	MP:0008126	increased dendritic cell number	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	25447050
MGI:2658880	F	MP:0002970	abnormal white adipose tissue morphology	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	25447050
MGI:2658880	F	MP:0000613	abnormal salivary gland morphology	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	25447050
MGI:2658880	F	MP:0001126	abnormal ovary morphology	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	9826549
MGI:2658880	F	MP:0003572	abnormal uterus development	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	9826549
MGI:2658880	F	MP:0004905	decreased uterus weight	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	9826549
MGI:2658880	F	MP:0001870	salivary gland inflammation	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv	N	25447050
MGI:2658930	F	MP:0002637	small uterus	Cyp27b1<tm1Dgo>/Cyp27b1<tm1Dgo>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	11416220
MGI:2658930	F	MP:0001130	abnormal ovarian folliculogenesis	Cyp27b1<tm1Dgo>/Cyp27b1<tm1Dgo>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	11416220
MGI:2658930	F	MP:0001127	small ovary	Cyp27b1<tm1Dgo>/Cyp27b1<tm1Dgo>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	11416220
MGI:2658930	F	MP:0008869	anovulation	Cyp27b1<tm1Dgo>/Cyp27b1<tm1Dgo>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	11416220
MGI:2658930	F	MP:0001132	absent mature ovarian follicles	Cyp27b1<tm1Dgo>/Cyp27b1<tm1Dgo>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	11416220
MGI:2658930	F	MP:0009091	endometrium hypoplasia	Cyp27b1<tm1Dgo>/Cyp27b1<tm1Dgo>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	11416220
MGI:2658930	F	MP:0009009	absent estrous cycle	Cyp27b1<tm1Dgo>/Cyp27b1<tm1Dgo>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	11416220
MGI:2658930	F	MP:0001926	female infertility	Cyp27b1<tm1Dgo>/Cyp27b1<tm1Dgo>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	11416220
MGI:2658930	F	MP:0001134	absent corpus luteum	Cyp27b1<tm1Dgo>/Cyp27b1<tm1Dgo>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	11416220
MGI:2659009	M	MP:0001152	increased Leydig cell number	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9843206
MGI:2659009	M	MP:0006420	abnormal peritubular myoid cell morphology	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0006419	disorganized testis cords	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12538527
MGI:2659009	M	MP:0001154	seminiferous tubule degeneration	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9843206
MGI:2659009	M	MP:0006427	ectopic Leydig cells	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0006427	ectopic Leydig cells	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12538527
MGI:2659009	M	MP:0013603	abnormal fetal Leydig cell differentiation	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12538527
MGI:2659009	M	MP:0004728	abnormal efferent ductules of testis morphology	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0001154	seminiferous tubule degeneration	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9843206
MGI:2659009	M	MP:0031407	increased Sertoli cell proliferation	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0004852	decreased testis weight	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0009257	dilated seminiferous tubule	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0006262	increased testis tumor incidence	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0006418	abnormal testis cord formation	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12538527
MGI:2659009	M	MP:0006417	rete testis obstruction	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0004109	abnormal Sertoli cell development	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12538527
MGI:2659009	M	MP:0008297	retention of the adrenal gland x-zone	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9843206
MGI:2659009	M	MP:0005379	endocrine/exocrine gland phenotype	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	Y	9843206
MGI:2659009	M	MP:0002786	abnormal Leydig cell morphology	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0001147	small testis	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9843206
MGI:2659009	M	MP:0001925	male infertility	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9843206
MGI:2659009	M	MP:0001146	abnormal testis morphology	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9843206
MGI:2659009	M	MP:0006428	ectopic Sertoli cells	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0001925	male infertility	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0002118	abnormal lipid homeostasis	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0004852	decreased testis weight	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9843206
MGI:2659009	M	MP:0004806	absent germ cells	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9843206
MGI:2659009	M	MP:0001156	abnormal spermatogenesis	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9843206
MGI:2659009	M	MP:0004901	decreased male germ cell number	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9843206
MGI:2659009	M	MP:0001152	increased Leydig cell number	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	11564714
MGI:2659009	M	MP:0006421	decreased number of peritubular myoid cells	Nr0b1<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	12538527
MGI:2659012	F	MP:0009433	polyovular ovarian follicle	Nr0b1<tm1.1Lja>/Nr0b1<tm1.1Lja>	involves: 129S1/Sv * 129X1/SvJ	N	9843206
MGI:2659051	F	MP:0001127	small ovary	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	N	9288969
MGI:2659051	M	MP:0001147	small testis	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	N	9288969
MGI:2659051	M	MP:0001925	male infertility	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	N	9288969
MGI:2659051	F	MP:0002777	absent ovarian follicles	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	N	9288969
MGI:2659051	M	MP:0002216	abnormal seminiferous tubule morphology	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	N	11514340
MGI:2659051	M	MP:0002216	abnormal seminiferous tubule morphology	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	N	9288969
MGI:2659051	F	MP:0001926	female infertility	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	N	9288969
MGI:2659051	M	MP:0001155	arrest of spermatogenesis	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	N	11514340
MGI:2659051	M	MP:0001155	arrest of spermatogenesis	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	N	9288969
MGI:2659052	M	MP:0006362	abnormal male germ cell morphology	Dazl<tm1Hjc>/Dazl<+>	involves: 129P2/OlaHsd * MF1	N	9288969
MGI:2659052	M	MP:0002687	oligozoospermia	Dazl<tm1Hjc>/Dazl<+>	involves: 129P2/OlaHsd * MF1	N	9288969
MGI:2659065	F	MP:0001290	delayed eyelid opening	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659065	F	MP:0000448	pointed snout	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659065	F	MP:0000433	microcephaly	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659065	F	MP:0000455	abnormal maxilla morphology	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659065	F	MP:0004174	abnormal spine curvature	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659065	F	MP:0001732	postnatal growth retardation	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659065	F	MP:0002082	postnatal lethality	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659065	F	MP:0030273	mandibular retrognathia	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659065	F	MP:0000088	short mandible	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659065	F	MP:0000585	kinked tail	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659066	M	MP:0002216	abnormal seminiferous tubule morphology	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	N	8805249
MGI:2659066	M	MP:0005159	azoospermia	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	N	8805249
MGI:2659066	M	MP:0001925	male infertility	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	N	8805249
MGI:2659066	M	MP:0002784	abnormal Sertoli cell morphology	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	N	8805249
MGI:2659066	M	MP:0006380	abnormal spermatid morphology	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	N	8805249
MGI:2659066	M	MP:0001155	arrest of spermatogenesis	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	N	8805249
MGI:2659066	M	MP:0001147	small testis	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	N	8805249
MGI:2659067	M	MP:0001147	small testis	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	N	8805249
MGI:2659067	M	MP:0002784	abnormal Sertoli cell morphology	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	N	8805249
MGI:2659067	M	MP:0005159	azoospermia	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	N	8805249
MGI:2659067	M	MP:0002216	abnormal seminiferous tubule morphology	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	N	8805249
MGI:2659067	M	MP:0008279	arrest of spermiogenesis	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	N	8805249
MGI:2659067	M	MP:0001156	abnormal spermatogenesis	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	N	8805249
MGI:2659067	M	MP:0001925	male infertility	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	N	8805249
MGI:2659073	M	MP:0009655	abnormal secondary palate development	Cask<Tg(Bnlf1)1Wln>/Y	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659073	M	MP:0009888	palatal shelves fail to meet at midline	Cask<Tg(Bnlf1)1Wln>/Y	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659073	M	MP:0000455	abnormal maxilla morphology	Cask<Tg(Bnlf1)1Wln>/Y	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659073	M	MP:0031462	decreased palatal shelf size	Cask<Tg(Bnlf1)1Wln>/Y	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659073	M	MP:0000433	microcephaly	Cask<Tg(Bnlf1)1Wln>/Y	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659073	M	MP:0000448	pointed snout	Cask<Tg(Bnlf1)1Wln>/Y	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659073	M	MP:0011087	neonatal lethality, complete penetrance	Cask<Tg(Bnlf1)1Wln>/Y	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659073	M	MP:0030273	mandibular retrognathia	Cask<Tg(Bnlf1)1Wln>/Y	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659073	M	MP:0009890	cleft secondary palate	Cask<Tg(Bnlf1)1Wln>/Y	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659073	M	MP:0000088	short mandible	Cask<Tg(Bnlf1)1Wln>/Y	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659073	M	MP:0001436	abnormal suckling behavior	Cask<Tg(Bnlf1)1Wln>/Y	involves: C57BL/6J * DBA/2J	N	8494785
MGI:2659075	F	MP:0001923	reduced female fertility	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0001732	postnatal growth retardation	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0000448	pointed snout	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0004174	abnormal spine curvature	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0030273	mandibular retrognathia	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0000585	kinked tail	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0000088	short mandible	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0000433	microcephaly	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0001222	epidermal hyperplasia	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0001505	hunched posture	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0001290	delayed eyelid opening	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0001211	wrinkled skin	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0000418	focal hair loss	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0002083	premature death	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0001935	decreased litter size	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0000378	absent hair follicles	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659075	F	MP:0000455	abnormal maxilla morphology	Cask<Tg(Bnlf1)1Wln>/Cask<Tg(Bnlf1)1Wln>	involves: C57BL/6J * CD-1 * DBA/2J	N	8494785
MGI:2659090	M	MP:0001146	abnormal testis morphology	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0001925	male infertility	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0001751	increased circulating luteinizing hormone level	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0002286	cryptorchism	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0006362	abnormal male germ cell morphology	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0001147	small testis	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0002786	abnormal Leydig cell morphology	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0005189	abnormal anogenital distance	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0002780	decreased circulating testosterone level	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0006418	abnormal testis cord formation	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0006379	abnormal spermatocyte morphology	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0002789	male pseudohermaphroditism	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0002784	abnormal Sertoli cell morphology	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0005536	decreased Leydig cell number	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0002216	abnormal seminiferous tubule morphology	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0001156	abnormal spermatogenesis	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0004852	decreased testis weight	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0006420	abnormal peritubular myoid cell morphology	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0006421	decreased number of peritubular myoid cells	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0001152	increased Leydig cell number	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659090	M	MP:0006378	abnormal spermatogonia morphology	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	N	11090455
MGI:2659187	F	MP:0000662	abnormal branching of the mammary ductal tree	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	9384572
MGI:2659187	F	MP:0001728	failure of embryo implantation	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	9384572
MGI:2659187	F	MP:0000627	abnormal mammary gland morphology	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	9384572
MGI:2659187	M	MP:0031362	decreased prostate gland ventral lobe weight	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	9724019
MGI:2659187	F	MP:0001927	abnormal estrous cycle	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	9384572
MGI:2659187	F	MP:0009017	prolonged estrus	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	9384572
MGI:2659187	F	MP:0009007	short estrous cycle	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	9384572
MGI:2659187	M	MP:0008939	increased pituitary gland weight	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	9724019
MGI:2659187	M	MP:0004910	decreased seminal vesicle weight	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	9724019
MGI:2659187	F	MP:0009014	prolonged proestrus	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	9384572
MGI:2659187	F	MP:0005386	behavior/neurological phenotype	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	Y	9384572
MGI:2659187	F	MP:0009006	prolonged estrous cycle	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	9384572
MGI:2659187	F	MP:0000628	abnormal mammary gland development	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	9384572
MGI:2659187	F	MP:0013336	pituitary gland hypertrophy	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	12399440
MGI:2659187	F	MP:0000633	abnormal pituitary gland morphology	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	12399440
MGI:2659187	F	MP:0001926	female infertility	Prl<tm1Hmn>/Prl<tm1Hmn>	involves: 129S2/SvPas	N	9384572
MGI:2660566	M	MP:0001925	male infertility	Ddx4<tm1Tnc>/Ddx4<tm1Tnc>	involves: 129P2/OlaHsd * C57BL/6NJcl	N	10766740
MGI:2660566	M	MP:0008261	arrest of male meiosis	Ddx4<tm1Tnc>/Ddx4<tm1Tnc>	involves: 129P2/OlaHsd * C57BL/6NJcl	N	10766740
MGI:2660566	M	MP:0014052	increased male germ cell apoptosis	Ddx4<tm1Tnc>/Ddx4<tm1Tnc>	involves: 129P2/OlaHsd * C57BL/6NJcl	N	10766740
MGI:2660566	M	MP:0003205	testicular atrophy	Ddx4<tm1Tnc>/Ddx4<tm1Tnc>	involves: 129P2/OlaHsd * C57BL/6NJcl	N	10766740
MGI:2660566	M	MP:0001153	small seminiferous tubules	Ddx4<tm1Tnc>/Ddx4<tm1Tnc>	involves: 129P2/OlaHsd * C57BL/6NJcl	N	10766740
MGI:2660641	M	MP:0001922	reduced male fertility	Prlr<tm1Cnp>/Prlr<tm1Cnp>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660641	F	MP:0011988	increased mating frequency	Prlr<tm1Cnp>/Prlr<tm1Cnp>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660641	M	MP:0001925	male infertility	Prlr<tm1Cnp>/Prlr<tm1Cnp>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660641	F	MP:0001926	female infertility	Prlr<tm1Cnp>/Prlr<tm1Cnp>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660641	F	MP:0011125	decreased primary ovarian follicle number	Prlr<tm1Cnp>/Prlr<tm1Cnp>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660641	F	MP:0004014	abnormal uterine environment	Prlr<tm1Cnp>/Prlr<tm1Cnp>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660641	F	MP:0003845	abnormal decidualization	Prlr<tm1Cnp>/Prlr<tm1Cnp>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660641	F	MP:0004015	abnormal oviduct environment	Prlr<tm1Cnp>/Prlr<tm1Cnp>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660641	F	MP:0001931	abnormal oogenesis	Prlr<tm1Cnp>/Prlr<tm1Cnp>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660641	F	MP:0003355	decreased ovulation rate	Prlr<tm1Cnp>/Prlr<tm1Cnp>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660642	F	MP:0001386	abnormal maternal nurturing	Prlr<tm1Cnp>/Prlr<+>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660642	F	MP:0000628	abnormal mammary gland development	Prlr<tm1Cnp>/Prlr<+>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660642	F	MP:0001882	abnormal lactation	Prlr<tm1Cnp>/Prlr<+>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660642	F	MP:0001384	abnormal pup retrieval	Prlr<tm1Cnp>/Prlr<+>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	9009200
MGI:2660654	F	MP:0008779	abnormal maternal behavior	Prlr<tm1Cnp>/Prlr<tm1Cnp>	involves: 129P2/OlaHsd	N	9751488
MGI:2660654	F	MP:0001384	abnormal pup retrieval	Prlr<tm1Cnp>/Prlr<tm1Cnp>	involves: 129P2/OlaHsd	N	9751488
MGI:2660655	F	MP:0008779	abnormal maternal behavior	Prlr<tm1Cnp>/Prlr<+>	involves: 129P2/OlaHsd	N	9751488
MGI:2660655	F	MP:0001384	abnormal pup retrieval	Prlr<tm1Cnp>/Prlr<+>	involves: 129P2/OlaHsd	N	9751488
MGI:2660657	M	MP:0001925	male infertility	Runx1t1<tm1Fc>/Runx1t1<tm1Fc>	involves: 129S/SvEv * C57BL/6	N	11463846
MGI:2660658	F	MP:0009661	abnormal pregnancy	Cbs<tm1Unc>/Cbs<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	16984962
MGI:2660658	F	MP:0009012	short diestrus	Cbs<tm1Unc>/Cbs<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	16984962
MGI:2660658	F	MP:0008871	abnormal ovarian follicle number	Cbs<tm1Unc>/Cbs<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	16984962
MGI:2660658	F	MP:0009018	short estrus	Cbs<tm1Unc>/Cbs<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	16984962
MGI:2660658	F	MP:0009020	prolonged metestrus	Cbs<tm1Unc>/Cbs<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	16984962
MGI:2660658	F	MP:0004256	abnormal maternal decidual layer morphology	Cbs<tm1Unc>/Cbs<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	16984962
MGI:2660658	F	MP:0004903	abnormal uterus weight	Cbs<tm1Unc>/Cbs<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	16984962
MGI:2660658	F	MP:0004014	abnormal uterine environment	Cbs<tm1Unc>/Cbs<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	16984962
MGI:2660658	F	MP:0009007	short estrous cycle	Cbs<tm1Unc>/Cbs<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	16984962
MGI:2660658	F	MP:0001926	female infertility	Cbs<tm1Unc>/Cbs<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	16984962
MGI:2660658	F	MP:0001926	female infertility	Cbs<tm1Unc>/Cbs<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	7878023
MGI:2660690	F	MP:0001926	female infertility	Zp3<tm1Dean>/Zp3<tm1Dean>	involves: 129S4/SvJae * C57BL/6J	N	8787763
MGI:2660690	F	MP:0003697	absent zona pellucida	Zp3<tm1Dean>/Zp3<tm1Dean>	involves: 129S4/SvJae * C57BL/6J	N	8787763
MGI:2660690	F	MP:0001130	abnormal ovarian folliculogenesis	Zp3<tm1Dean>/Zp3<tm1Dean>	involves: 129S4/SvJae * C57BL/6J	N	8787763
MGI:2660690	F	MP:0031420	decreased superovulation rate	Zp3<tm1Dean>/Zp3<tm1Dean>	involves: 129S4/SvJae * C57BL/6J	N	8787763
MGI:2660694	F	MP:0001127	small ovary	Zp3<tm1Pmw>/Zp3<tm1Pmw>	involves: 129S1/Sv * C57BL/6J	N	9476659
MGI:2660694	F	MP:0011129	decreased tertiary ovarian follicle number	Zp3<tm1Pmw>/Zp3<tm1Pmw>	involves: 129S1/Sv * C57BL/6J	N	9476659
MGI:2660694	F	MP:0031420	decreased superovulation rate	Zp3<tm1Pmw>/Zp3<tm1Pmw>	involves: 129S1/Sv * C57BL/6J	N	9476659
MGI:2660694	F	MP:0001130	abnormal ovarian folliculogenesis	Zp3<tm1Pmw>/Zp3<tm1Pmw>	involves: 129S1/Sv * C57BL/6J	N	9476659
MGI:2660694	F	MP:0001926	female infertility	Zp3<tm1Pmw>/Zp3<tm1Pmw>	involves: 129S1/Sv * C57BL/6J	N	9476659
MGI:2660694	F	MP:0003697	absent zona pellucida	Zp3<tm1Pmw>/Zp3<tm1Pmw>	involves: 129S1/Sv * C57BL/6J	N	9476659
MGI:2660694	F	MP:0001926	female infertility	Zp3<tm1Pmw>/Zp3<tm1Pmw>	involves: 129S1/Sv * C57BL/6J	N	8643592
MGI:2660694	F	MP:0001125	abnormal oocyte morphology	Zp3<tm1Pmw>/Zp3<tm1Pmw>	involves: 129S1/Sv * C57BL/6J	N	9476659
MGI:2660694	F	MP:0031420	decreased superovulation rate	Zp3<tm1Pmw>/Zp3<tm1Pmw>	involves: 129S1/Sv * C57BL/6J	N	8643592
MGI:2660694	F	MP:0001127	small ovary	Zp3<tm1Pmw>/Zp3<tm1Pmw>	involves: 129S1/Sv * C57BL/6J	N	8643592
MGI:2660694	F	MP:0004856	decreased ovary weight	Zp3<tm1Pmw>/Zp3<tm1Pmw>	involves: 129S1/Sv * C57BL/6J	N	9476659
MGI:2660694	F	MP:0009372	abnormal cumulus oophorus morphology	Zp3<tm1Pmw>/Zp3<tm1Pmw>	involves: 129S1/Sv * C57BL/6J	N	8643592
MGI:2660694	F	MP:0003697	absent zona pellucida	Zp3<tm1Pmw>/Zp3<tm1Pmw>	involves: 129S1/Sv * C57BL/6J	N	8643592
MGI:2660696	F	MP:0009375	thin zona pellucida	Zp3<tm1Pmw>/Zp3<+>	involves: 129S1/Sv * C57BL/6J	N	9107049
MGI:2660715	F	MP:0002169	no abnormal phenotype detected	Bmx<tm1Ali>/Bmx<tm1Ali>	involves: 129S1/Sv * 129X1/SvJ * DBA/2	N	11416142
MGI:2660751	F	MP:0001129	impaired ovarian folliculogenesis	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	8373945
MGI:2660751	M	MP:0002687	oligozoospermia	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	F	MP:0001127	small ovary	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	8373945
MGI:2660751	F	MP:0009226	small uterine cervix	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	F	MP:0001129	impaired ovarian folliculogenesis	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	F	MP:0001119	abnormal female reproductive system morphology	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	F	MP:0001927	abnormal estrous cycle	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	8373945
MGI:2660751	F	MP:0001127	small ovary	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	F	MP:0002637	small uterus	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	F	MP:0002637	small uterus	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	8373945
MGI:2660751	F	MP:0009009	absent estrous cycle	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	8373945
MGI:2660751	M	MP:0004930	small epididymis	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	M	MP:0001147	small testis	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	F	MP:0031420	decreased superovulation rate	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	8373945
MGI:2660751	F	MP:0001926	female infertility	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	8373945
MGI:2660751	F	MP:0001926	female infertility	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	M	MP:0002216	abnormal seminiferous tubule morphology	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	M	MP:0001925	male infertility	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	F	MP:0002016	ovary cyst	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	F	MP:0009094	abnormal endometrial gland morphology	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	8373945
MGI:2660751	F	MP:0002680	decreased corpora lutea number	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	F	MP:0008257	thin myometrium	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	1924340
MGI:2660751	F	MP:0008257	thin myometrium	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	8373945
MGI:2660751	F	MP:0031422	failure of superovulation	Fancl<gcd>/Fancl<gcd>	involves: C57BL/6J * CBA/J	N	8373945
MGI:2660790	M	MP:0001925	male infertility	Fancl<gcd>/Fancl<tm1Ceb>	involves: 129/Sv * C57BL/6 * FVB/N	N	12417526
MGI:2660790	M	MP:0001147	small testis	Fancl<gcd>/Fancl<tm1Ceb>	involves: 129/Sv * C57BL/6 * FVB/N	N	12417526
MGI:2660790	M	MP:0002784	abnormal Sertoli cell morphology	Fancl<gcd>/Fancl<tm1Ceb>	involves: 129/Sv * C57BL/6 * FVB/N	N	12417526
MGI:2660790	F	MP:0001926	female infertility	Fancl<gcd>/Fancl<tm1Ceb>	involves: 129/Sv * C57BL/6 * FVB/N	N	12417526
MGI:2660795	M	MP:0001925	male infertility	Fancl<tm1Ceb>/Fancl<tm1Ceb>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * FVB/N)	N	12417526
MGI:2660795	F	MP:0002637	small uterus	Fancl<tm1Ceb>/Fancl<tm1Ceb>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * FVB/N)	N	12417526
MGI:2660795	F	MP:0001127	small ovary	Fancl<tm1Ceb>/Fancl<tm1Ceb>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * FVB/N)	N	12417526
MGI:2660795	M	MP:0001147	small testis	Fancl<tm1Ceb>/Fancl<tm1Ceb>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * FVB/N)	N	12417526
MGI:2660795	M	MP:0004901	decreased male germ cell number	Fancl<tm1Ceb>/Fancl<tm1Ceb>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * FVB/N)	N	12417526
MGI:2660795	F	MP:0001926	female infertility	Fancl<tm1Ceb>/Fancl<tm1Ceb>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * FVB/N)	N	12417526
MGI:2660795	M	MP:0002216	abnormal seminiferous tubule morphology	Fancl<tm1Ceb>/Fancl<tm1Ceb>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * FVB/N)	N	12417526
MGI:2660795	F	MP:0001129	impaired ovarian folliculogenesis	Fancl<tm1Ceb>/Fancl<tm1Ceb>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * FVB/N)	N	12417526
MGI:2660806	F	MP:0001926	female infertility	Tial1<tm1Mst>/Tial1<tm1Mst>	involves: 129S2/SvPas * C57BL/6	N	9482885
MGI:2660806	F	MP:0002777	absent ovarian follicles	Tial1<tm1Mst>/Tial1<tm1Mst>	involves: 129S2/SvPas * C57BL/6	N	9482885
MGI:2660806	F	MP:0001127	small ovary	Tial1<tm1Mst>/Tial1<tm1Mst>	involves: 129S2/SvPas * C57BL/6	N	9482885
MGI:2660806	M	MP:0001147	small testis	Tial1<tm1Mst>/Tial1<tm1Mst>	involves: 129S2/SvPas * C57BL/6	N	9482885
MGI:2660806	M	MP:0001925	male infertility	Tial1<tm1Mst>/Tial1<tm1Mst>	involves: 129S2/SvPas * C57BL/6	N	9482885
MGI:2660806	F	MP:0001128	ovary hyperplasia	Tial1<tm1Mst>/Tial1<tm1Mst>	involves: 129S2/SvPas * C57BL/6	N	9482885
MGI:2661087	M	MP:0002675	asthenozoospermia	Adcy3<tm1Drs>/Adcy3<tm1Drs>	involves: 129X1/SvJ * C57BL/6	N	15705663
MGI:2661087	M	MP:0001922	reduced male fertility	Adcy3<tm1Drs>/Adcy3<tm1Drs>	involves: 129X1/SvJ * C57BL/6	N	15705663
MGI:2661087	F	MP:0001923	reduced female fertility	Adcy3<tm1Drs>/Adcy3<tm1Drs>	involves: 129X1/SvJ * C57BL/6	N	15705663
MGI:2661087	M	MP:0003666	impaired sperm capacitation	Adcy3<tm1Drs>/Adcy3<tm1Drs>	involves: 129X1/SvJ * C57BL/6	N	15705663
MGI:2661087	M	MP:0013288	premature acrosome reaction	Adcy3<tm1Drs>/Adcy3<tm1Drs>	involves: 129X1/SvJ * C57BL/6	N	15705663
MGI:2661436	M	MP:0001925	male infertility	Agtpbp1<pcd-5J>/Agtpbp1<pcd-5J>	involves: DBA/2J	N	16465590
MGI:2661729	F	MP:0005140	decreased cardiac muscle contractility	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6	N	12075344
MGI:2661730	M	MP:0001853	heart inflammation	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:2661730	M	MP:0001544	abnormal cardiovascular system physiology	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:2661730	M	MP:0006138	congestive heart failure	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:2661730	M	MP:0003819	increased left ventricle diastolic pressure	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:2661730	M	MP:0002753	dilated heart left ventricle	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:2661730	M	MP:0011925	abnormal heart echocardiography feature	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:2661730	M	MP:0008713	abnormal cytokine level	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:2661730	M	MP:0001596	hypotension	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12075344
MGI:2661730	M	MP:0021158	decreased heart left ventricle wall thickness	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12075344
MGI:2661730	M	MP:0003674	oxidative stress	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:2661730	M	MP:0008022	dilated heart ventricle	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:2661730	M	MP:0001625	cardiac hypertrophy	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:2661730	M	MP:0020446	increased NAD(P)H oxidase activity	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:2661730	M	MP:0005140	decreased cardiac muscle contractility	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:2661730	M	MP:0005140	decreased cardiac muscle contractility	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12075344
MGI:2661730	M	MP:0002795	dilated cardiomyopathy	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:2661733	M	MP:0031228	decreased angiotensin II level	Ace<tm1Unc>/Ace<tm1Unc>,Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	16001071
MGI:2661733	M	MP:0005166	decreased susceptibility to injury	Ace<tm1Unc>/Ace<tm1Unc>,Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	16001071
MGI:2661733	M	MP:0002135	abnormal kidney morphology	Ace<tm1Unc>/Ace<tm1Unc>,Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	12075344
MGI:2661733	M	MP:0031231	decreased circulating angiotensin II level	Ace<tm1Unc>/Ace<tm1Unc>,Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	16001071
MGI:2661733	M	MP:0001596	hypotension	Ace<tm1Unc>/Ace<tm1Unc>,Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	12075344
MGI:2661736	F	MP:0031231	decreased circulating angiotensin II level	Ace<tm1Unc>/Ace<tm1Unc>,Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	16001071
MGI:2661736	F	MP:0031228	decreased angiotensin II level	Ace<tm1Unc>/Ace<tm1Unc>,Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	16001071
MGI:2661736	F	MP:0005166	decreased susceptibility to injury	Ace<tm1Unc>/Ace<tm1Unc>,Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	16001071
MGI:2661736	F	MP:0002135	abnormal kidney morphology	Ace<tm1Unc>/Ace<tm1Unc>,Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	12075344
MGI:2661736	F	MP:0001596	hypotension	Ace<tm1Unc>/Ace<tm1Unc>,Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	12075344
MGI:2661773	M	MP:0030976	impaired sperm penetration of zona pellucida	Apob<tm1Bres>/Apob<+>	involves: 129S4/SvJae * C57BL/6J	N	8855280
MGI:2661773	M	MP:0001922	reduced male fertility	Apob<tm1Bres>/Apob<+>	involves: 129S4/SvJae * C57BL/6J	N	8855280
MGI:2661773	M	MP:0002687	oligozoospermia	Apob<tm1Bres>/Apob<+>	involves: 129S4/SvJae * C57BL/6J	N	8855280
MGI:2661773	M	MP:0002675	asthenozoospermia	Apob<tm1Bres>/Apob<+>	involves: 129S4/SvJae * C57BL/6J	N	8855280
MGI:2661849	F	MP:0011120	increased primordial ovarian follicle number	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10614669
MGI:2661863	F	MP:0002680	decreased corpora lutea number	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	N	10910997
MGI:2661863	F	MP:0001130	abnormal ovarian folliculogenesis	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	N	12606443
MGI:2661863	F	MP:0000662	abnormal branching of the mammary ductal tree	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	N	9772216
MGI:2661863	F	MP:0011129	decreased tertiary ovarian follicle number	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	N	10910997
MGI:2661863	F	MP:0031381	decreased secondary ovarian follicle number	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	N	10910997
MGI:2661863	F	MP:0031381	decreased secondary ovarian follicle number	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	N	12606443
MGI:2661863	F	MP:0001928	abnormal ovulation	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	N	12606443
MGI:2661863	F	MP:0011129	decreased tertiary ovarian follicle number	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	N	12606443
MGI:2661863	F	MP:0001127	small ovary	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	N	12606443
MGI:2661863	F	MP:0003507	abnormal ovary physiology	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	N	17594909
MGI:2661863	F	MP:0031420	decreased superovulation rate	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	N	17594909
MGI:2661863	F	MP:0011120	increased primordial ovarian follicle number	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	N	10910997
MGI:2661863	F	MP:0004856	decreased ovary weight	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	N	17594909
MGI:2661881	M	MP:0001925	male infertility	Styx<tm1Jedi>/Styx<tm1Jedi>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	N	11842224
MGI:2661881	M	MP:0005578	teratozoospermia	Styx<tm1Jedi>/Styx<tm1Jedi>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	N	11842224
MGI:2661881	M	MP:0006380	abnormal spermatid morphology	Styx<tm1Jedi>/Styx<tm1Jedi>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	N	11842224
MGI:2661881	M	MP:0001156	abnormal spermatogenesis	Styx<tm1Jedi>/Styx<tm1Jedi>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	N	11842224
MGI:2661881	M	MP:0002675	asthenozoospermia	Styx<tm1Jedi>/Styx<tm1Jedi>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	N	11842224
MGI:2661881	M	MP:0002686	globozoospermia	Styx<tm1Jedi>/Styx<tm1Jedi>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	N	11842224
MGI:2661882	M	MP:0001156	abnormal spermatogenesis	Styx<tm1.1Jedi>/Styx<tm1.1Jedi>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	N	11842224
MGI:2661882	M	MP:0001925	male infertility	Styx<tm1.1Jedi>/Styx<tm1.1Jedi>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	N	11842224
MGI:2661882	M	MP:0002675	asthenozoospermia	Styx<tm1.1Jedi>/Styx<tm1.1Jedi>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	N	11842224
MGI:2661899	F	MP:0001134	absent corpus luteum	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	10976923
MGI:2661899	F	MP:0004832	enlarged ovary	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	10976923
MGI:2661899	M	MP:0002789	male pseudohermaphroditism	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	9326645
MGI:2661899	M	MP:0002789	male pseudohermaphroditism	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	10976923
MGI:2661899	F	MP:0001120	abnormal uterus morphology	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	10976923
MGI:2661899	F	MP:0001126	abnormal ovary morphology	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	10976923
MGI:2661899	M	MP:0002786	abnormal Leydig cell morphology	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	10976923
MGI:2661899	M	MP:0002786	abnormal Leydig cell morphology	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	9326645
MGI:2661899	F	MP:0001130	abnormal ovarian folliculogenesis	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	10976923
MGI:2661899	M	MP:0002774	small prostate gland	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	9326645
MGI:2661899	M	MP:0001152	increased Leydig cell number	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	10976923
MGI:2661899	M	MP:0005148	seminal vesicle hypoplasia	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	9326645
MGI:2661899	M	MP:0002774	small prostate gland	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	10976923
MGI:2661899	M	MP:0005147	prostate gland hypoplasia	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	9326645
MGI:2661899	M	MP:0001157	small seminal vesicle	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	10976923
MGI:2661899	M	MP:0001155	arrest of spermatogenesis	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	10976923
MGI:2661899	M	MP:0001146	abnormal testis morphology	Star<tm1Klp>/Star<tm1Klp>	involves: 129P2/OlaHsd	N	9326645
MGI:2661938	M	MP:0001922	reduced male fertility	Pou5f2<tm1Rsd>/Pou5f2<tm1Rsd>	involves: 129S4/SvJae	N	9207130
MGI:2661940	F	MP:0002680	decreased corpora lutea number	Ccs<tm1Pcw>/Ccs<tm1Pcw>	involves: 129S1/Sv	N	10694572
MGI:2661940	F	MP:0002682	decreased mature ovarian follicle number	Ccs<tm1Pcw>/Ccs<tm1Pcw>	involves: 129S1/Sv	N	10694572
MGI:2661940	F	MP:0001923	reduced female fertility	Ccs<tm1Pcw>/Ccs<tm1Pcw>	involves: 129S1/Sv	N	10694572
MGI:2661940	F	MP:0001131	abnormal ovarian follicle morphology	Ccs<tm1Pcw>/Ccs<tm1Pcw>	involves: 129S1/Sv	N	10694572
MGI:2661963	M	MP:0002769	abnormal vas deferens morphology	Insl3<tm1Par>/Insl3<tm1Par>	involves: 129/Sv * CD-1	N	10391220
MGI:2661963	M	MP:0001147	small testis	Insl3<tm1Par>/Insl3<tm1Par>	involves: 129/Sv * CD-1	N	10391220
MGI:2661963	M	MP:0006380	abnormal spermatid morphology	Insl3<tm1Par>/Insl3<tm1Par>	involves: 129/Sv * CD-1	N	10391220
MGI:2661963	F	MP:0009006	prolonged estrous cycle	Insl3<tm1Par>/Insl3<tm1Par>	involves: 129/Sv * CD-1	N	10391220
MGI:2661963	M	MP:0001925	male infertility	Insl3<tm1Par>/Insl3<tm1Par>	involves: 129/Sv * CD-1	N	10391220
MGI:2661963	M	MP:0020550	multinucleated giant male germ cells	Insl3<tm1Par>/Insl3<tm1Par>	involves: 129/Sv * CD-1	N	10391220
MGI:2661963	M	MP:0001156	abnormal spermatogenesis	Insl3<tm1Par>/Insl3<tm1Par>	involves: 129/Sv * CD-1	N	10391220
MGI:2661963	M	MP:0001145	abnormal male reproductive system morphology	Insl3<tm1Par>/Insl3<tm1Par>	involves: 129/Sv * CD-1	N	10391220
MGI:2661963	M	MP:0031287	bilateral cryptorchism	Insl3<tm1Par>/Insl3<tm1Par>	involves: 129/Sv * CD-1	N	10391220
MGI:2661963	F	MP:0001926	female infertility	Insl3<tm1Par>/Insl3<tm1Par>	involves: 129/Sv * CD-1	N	10391220
MGI:2661986	M	MP:0008813	decreased common myeloid progenitor cell number	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0000689	abnormal spleen morphology	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0001861	lung inflammation	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0010901	abnormal pulmonary alveolar parenchyma morphology	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0003179	thrombocytopenia	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0013501	increased fibroblast apoptosis	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0005016	decreased lymphocyte cell number	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0008477	decreased spleen red pulp amount	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0000240	extramedullary hematopoiesis	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0000333	decreased bone marrow cell number	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0000691	enlarged spleen	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0010384	increased renal carcinoma incidence	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0030927	decreased telomere length	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0002270	abnormal pulmonary alveolus morphology	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0002874	decreased hemoglobin content	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0005264	glomerulosclerosis	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0005621	abnormal cell physiology	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0001577	anemia	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0005017	decreased B cell number	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0009278	abnormal bone marrow cell physiology	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0000221	decreased leukocyte cell number	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0014473	increased pulmonary alveolus wall thickness	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0001239	abnormal epidermis stratum granulosum morphology	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0001236	abnormal epidermis stratum spinosum morphology	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0002018	increased malignant tumor incidence	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0003426	pulmonary interstitial fibrosis	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0001883	increased mammary adenocarcinoma incidence	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0004756	abnormal proximal convoluted tubule morphology	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0010363	increased fibrosarcoma incidence	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0002023	increased B cell derived lymphoma incidence	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0008479	decreased spleen white pulp amount	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0011346	renal tubule atrophy	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0002123	abnormal definitive hematopoiesis	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0002050	increased pheochromocytoma incidence	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0008973	decreased erythroid progenitor cell number	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0001222	epidermal hyperplasia	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0010024	increased total body fat amount	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0009563	dyskeratosis	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0008209	decreased pre-B cell number	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661986	M	MP:0008714	increased lung carcinoma incidence	Dkc1<tm1Ppp>/Y	involves: 129S1/Sv	N	12522253
MGI:2661992	M	MP:0031286	unilateral cryptorchism	Insl3<tm1Par>/Insl3<+>	involves: 129/Sv * CD-1	N	10391220
MGI:2661992	M	MP:0002286	cryptorchism	Insl3<tm1Par>/Insl3<+>	involves: 129/Sv * CD-1	N	10391220
MGI:2661992	M	MP:0031287	bilateral cryptorchism	Insl3<tm1Par>/Insl3<+>	involves: 129/Sv * CD-1	N	10391220
MGI:2662000	M	MP:0001156	abnormal spermatogenesis	Insl3<tm1Imad>/Insl3<tm1Imad>	involves: 129/Sv * CD-1	N	10319319
MGI:2662000	M	MP:0001925	male infertility	Insl3<tm1Imad>/Insl3<tm1Imad>	involves: 129/Sv * CD-1	N	10319319
MGI:2662000	M	MP:0031287	bilateral cryptorchism	Insl3<tm1Imad>/Insl3<tm1Imad>	involves: 129/Sv * CD-1	N	10319319
MGI:2662011	M	MP:0031287	bilateral cryptorchism	Ar<Tfm>/Y,Insl3<tm1Imad>/Insl3<tm1Imad>	involves: 129/Sv * CD-1 * STOCK Eda<Ta>	N	10319319
MGI:2662011	M	MP:0003557	absent vas deferens	Ar<Tfm>/Y,Insl3<tm1Imad>/Insl3<tm1Imad>	involves: 129/Sv * CD-1 * STOCK Eda<Ta>	N	10319319
MGI:2662011	M	MP:0004727	absent epididymis	Ar<Tfm>/Y,Insl3<tm1Imad>/Insl3<tm1Imad>	involves: 129/Sv * CD-1 * STOCK Eda<Ta>	N	10319319
MGI:2662011	M	MP:0002789	male pseudohermaphroditism	Ar<Tfm>/Y,Insl3<tm1Imad>/Insl3<tm1Imad>	involves: 129/Sv * CD-1 * STOCK Eda<Ta>	N	10319319
MGI:2662011	M	MP:0005149	abnormal gubernaculum morphology	Ar<Tfm>/Y,Insl3<tm1Imad>/Insl3<tm1Imad>	involves: 129/Sv * CD-1 * STOCK Eda<Ta>	N	10319319
MGI:2662011	M	MP:0002212	abnormal secondary sex determination	Ar<Tfm>/Y,Insl3<tm1Imad>/Insl3<tm1Imad>	involves: 129/Sv * CD-1 * STOCK Eda<Ta>	N	10319319
MGI:2662011	M	MP:0001145	abnormal male reproductive system morphology	Ar<Tfm>/Y,Insl3<tm1Imad>/Insl3<tm1Imad>	involves: 129/Sv * CD-1 * STOCK Eda<Ta>	N	10319319
MGI:2662011	F	MP:0001119	abnormal female reproductive system morphology	Ar<Tfm>/Y,Insl3<tm1Imad>/Insl3<tm1Imad>	involves: 129/Sv * CD-1 * STOCK Eda<Ta>	N	10319319
MGI:2662181	M	MP:0002286	cryptorchism	Insl3<tm1Imad>/Insl3<tm1Imad>	involves: 129	N	10319319
MGI:2662272	F	MP:0001884	mammary gland alveolar hyperplasia	Cdh3<tm1Hyn>/Cdh3<tm1Hyn>	involves: 129S2/SvPas * C57BL/6	N	9362520
MGI:2662272	F	MP:0000627	abnormal mammary gland morphology	Cdh3<tm1Hyn>/Cdh3<tm1Hyn>	involves: 129S2/SvPas * C57BL/6	N	9362520
MGI:2662272	F	MP:0000628	abnormal mammary gland development	Cdh3<tm1Hyn>/Cdh3<tm1Hyn>	involves: 129S2/SvPas * C57BL/6	N	9362520
MGI:2662272	F	MP:0001885	mammary gland duct hyperplasia	Cdh3<tm1Hyn>/Cdh3<tm1Hyn>	involves: 129S2/SvPas * C57BL/6	N	9362520
MGI:2662272	F	MP:0000630	mammary gland hyperplasia	Cdh3<tm1Hyn>/Cdh3<tm1Hyn>	involves: 129S2/SvPas * C57BL/6	N	9362520
MGI:2662287	F	MP:0004855	increased ovary weight	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S7/SvEvBrd * C57BL/6	N	17652186
MGI:2662287	M	MP:0001156	abnormal spermatogenesis	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S7/SvEvBrd * C57BL/6	N	1448148
MGI:2662287	M	MP:0006262	increased testis tumor incidence	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S7/SvEvBrd * C57BL/6	N	17652186
MGI:2662287	M	MP:0004851	increased testis weight	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S7/SvEvBrd * C57BL/6	N	17652186
MGI:2662287	F	MP:0004834	ovary hemorrhage	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S7/SvEvBrd * C57BL/6	N	1448148
MGI:2662287	M	MP:0001148	enlarged testis	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S7/SvEvBrd * C57BL/6	N	1448148
MGI:2662287	M	MP:0031407	increased Sertoli cell proliferation	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S7/SvEvBrd * C57BL/6	N	17652186
MGI:2662287	F	MP:0001131	abnormal ovarian follicle morphology	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S7/SvEvBrd * C57BL/6	N	1448148
MGI:2662287	F	MP:0008000	increased ovary tumor incidence	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S7/SvEvBrd * C57BL/6	N	17652186
MGI:2662287	M	MP:0001925	male infertility	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S7/SvEvBrd * C57BL/6	N	1448148
MGI:2662287	F	MP:0008000	increased ovary tumor incidence	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S7/SvEvBrd * C57BL/6	N	1448148
MGI:2662287	F	MP:0001926	female infertility	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S7/SvEvBrd * C57BL/6	N	1448148
MGI:2662411	M	MP:0002687	oligozoospermia	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0008898	abnormal acrosome morphology	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0004182	abnormal spermiation	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0001156	abnormal spermatogenesis	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0002675	asthenozoospermia	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0002686	globozoospermia	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0005578	teratozoospermia	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0009232	abnormal sperm nucleus morphology	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0001922	reduced male fertility	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0008892	abnormal sperm flagellum morphology	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0020550	multinucleated giant male germ cells	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0031408	multi-headed sperm	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0001932	abnormal spermiogenesis	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0006379	abnormal spermatocyte morphology	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0008545	absent sperm flagellum	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0009230	abnormal sperm head morphology	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662411	M	MP:0009839	multiflagellated sperm	Gmcl1<Gt(OST6847)Lex>/Gmcl1<Gt(OST6847)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12556490
MGI:2662433	M	MP:0001925	male infertility	Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	10894153
MGI:2662433	F	MP:0001130	abnormal ovarian folliculogenesis	Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	10894153
MGI:2662433	M	MP:0005159	azoospermia	Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	10894153
MGI:2662433	M	MP:0001156	abnormal spermatogenesis	Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	10894153
MGI:2662434	F	MP:0001126	abnormal ovary morphology	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac	N	12205030
MGI:2662434	F	MP:0004834	ovary hemorrhage	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac	N	12205030
MGI:2662434	F	MP:0001134	absent corpus luteum	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac	N	12205030
MGI:2662434	F	MP:0009363	abnormal tertiary ovarian follicle morphology	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac	N	12205030
MGI:2662434	F	MP:0001129	impaired ovarian folliculogenesis	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac	N	12205030
MGI:2662434	F	MP:0002016	ovary cyst	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac	N	12205030
MGI:2662434	M	MP:0001922	reduced male fertility	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac	N	11545296
MGI:2662434	F	MP:0009364	abnormal mature ovarian follicle morphology	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac	N	12205030
MGI:2662434	M	MP:0001156	abnormal spermatogenesis	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac	N	11545296
MGI:2662434	M	MP:0002687	oligozoospermia	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac	N	11545296
MGI:2662434	M	MP:0002675	asthenozoospermia	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac	N	11545296
MGI:2662434	M	MP:0001380	reduced male mating frequency	Cyp19a1<tm1Esi>/Cyp19a1<tm1Esi>	involves: 129S6/SvEvTac	N	11545296
MGI:2662461	M	MP:0001940	testis hypoplasia	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	M	MP:0004852	decreased testis weight	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	F	MP:0001125	abnormal oocyte morphology	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	F	MP:0003572	abnormal uterus development	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	F	MP:0001923	reduced female fertility	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	F	MP:0031420	decreased superovulation rate	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	M	MP:0005536	decreased Leydig cell number	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	M	MP:0002675	asthenozoospermia	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	F	MP:0011130	absent tertiary ovarian follicles	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	M	MP:0002631	abnormal epididymis morphology	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	M	MP:0001922	reduced male fertility	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	F	MP:0004856	decreased ovary weight	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	M	MP:0002687	oligozoospermia	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	F	MP:0005158	ovary hypoplasia	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	F	MP:0031383	increased secondary ovarian follicle number	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	F	MP:0001130	abnormal ovarian folliculogenesis	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662461	F	MP:0003355	decreased ovulation rate	Sh2b1<tm1Ayos>/Sh2b1<tm1Ayos>	involves: C57BL/6	N	11940664
MGI:2662491	F	MP:0001923	reduced female fertility	Spag6l<tm1Jfs>/Spag6l<tm1Jfs>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:2662491	M	MP:0002675	asthenozoospermia	Spag6l<tm1Jfs>/Spag6l<tm1Jfs>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:2662491	M	MP:0008892	abnormal sperm flagellum morphology	Spag6l<tm1Jfs>/Spag6l<tm1Jfs>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:2662491	M	MP:0030590	abnormal sperm fibrous sheath morphology	Spag6l<tm1Jfs>/Spag6l<tm1Jfs>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:2662491	M	MP:0031356	abnormal outer dense fiber morphology	Spag6l<tm1Jfs>/Spag6l<tm1Jfs>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:2662491	M	MP:0005578	teratozoospermia	Spag6l<tm1Jfs>/Spag6l<tm1Jfs>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:2662491	M	MP:0009234	absent sperm head	Spag6l<tm1Jfs>/Spag6l<tm1Jfs>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:2662491	M	MP:0009836	abnormal sperm principal piece morphology	Spag6l<tm1Jfs>/Spag6l<tm1Jfs>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:2662491	M	MP:0001925	male infertility	Spag6l<tm1Jfs>/Spag6l<tm1Jfs>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:2662491	M	MP:0009831	abnormal sperm midpiece morphology	Spag6l<tm1Jfs>/Spag6l<tm1Jfs>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:2662491	M	MP:0009838	abnormal sperm axoneme morphology	Spag6l<tm1Jfs>/Spag6l<tm1Jfs>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:2662491	M	MP:0031352	absent sperm axonemal central pair	Spag6l<tm1Jfs>/Spag6l<tm1Jfs>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:2662491	M	MP:0009239	short sperm flagellum	Spag6l<tm1Jfs>/Spag6l<tm1Jfs>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:2662500	M	MP:0006423	dilated rete testis	Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	N	10880462
MGI:2662500	M	MP:0001154	seminiferous tubule degeneration	Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	N	10880462
MGI:2662500	F	MP:0000627	abnormal mammary gland morphology	Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	N	10880462
MGI:2662500	M	MP:0006262	increased testis tumor incidence	Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	N	10880462
MGI:2662500	M	MP:0001148	enlarged testis	Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	N	10880462
MGI:2662500	M	MP:0001146	abnormal testis morphology	Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	N	10880462
MGI:2662523	M	MP:0013602	abnormal Leydig cell differentiation	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	N	11287627
MGI:2662523	M	MP:0001925	male infertility	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	N	11287627
MGI:2662523	M	MP:0003205	testicular atrophy	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	N	11287627
MGI:2662523	M	MP:0002687	oligozoospermia	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	N	11287627
MGI:2662523	M	MP:0001154	seminiferous tubule degeneration	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	N	11287627
MGI:2662523	M	MP:0002675	asthenozoospermia	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	N	11287627
MGI:2662523	M	MP:0001152	increased Leydig cell number	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	N	11287627
MGI:2662523	M	MP:0001156	abnormal spermatogenesis	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	N	11287627
MGI:2662523	M	MP:0005169	abnormal male meiosis	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	N	11287627
MGI:2662543	M	MP:0005169	abnormal male meiosis	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6	N	11287627
MGI:2662543	M	MP:0002687	oligozoospermia	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6	N	11287627
MGI:2662543	M	MP:0001156	abnormal spermatogenesis	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6	N	11287627
MGI:2662555	M	MP:0005159	azoospermia	P2rx1<tm1Chn>/P2rx1<tm1Chn>	involves: 129P2/OlaHsd * MF1	N	10638758
MGI:2662555	M	MP:0002769	abnormal vas deferens morphology	P2rx1<tm1Chn>/P2rx1<tm1Chn>	involves: 129P2/OlaHsd * MF1	N	10638758
MGI:2662555	M	MP:0001925	male infertility	P2rx1<tm1Chn>/P2rx1<tm1Chn>	involves: 129P2/OlaHsd * MF1	N	10638758
MGI:2662563	F	MP:0001132	absent mature ovarian follicles	Cga<tm1Sac>/Cga<tm1Sac>	involves: 129S2/SvPas * C57BL/6J	N	7544315
MGI:2662563	F	MP:0002679	abnormal corpus luteum morphology	Cga<tm1Sac>/Cga<tm1Sac>	involves: 129S2/SvPas * C57BL/6J	N	7544315
MGI:2662563	M	MP:0001157	small seminal vesicle	Cga<tm1Sac>/Cga<tm1Sac>	involves: 129S2/SvPas * C57BL/6J	N	7544315
MGI:2662563	M	MP:0001147	small testis	Cga<tm1Sac>/Cga<tm1Sac>	involves: 129S2/SvPas * C57BL/6J	N	7544315
MGI:2662563	F	MP:0001129	impaired ovarian folliculogenesis	Cga<tm1Sac>/Cga<tm1Sac>	involves: 129S2/SvPas * C57BL/6J	N	7544315
MGI:2662563	M	MP:0008261	arrest of male meiosis	Cga<tm1Sac>/Cga<tm1Sac>	involves: 129S2/SvPas * C57BL/6J	N	7544315
MGI:2662563	M	MP:0001153	small seminiferous tubules	Cga<tm1Sac>/Cga<tm1Sac>	involves: 129S2/SvPas * C57BL/6J	N	7544315
MGI:2662563	F	MP:0001144	vagina atresia	Cga<tm1Sac>/Cga<tm1Sac>	involves: 129S2/SvPas * C57BL/6J	N	7544315
MGI:2662563	F	MP:0001926	female infertility	Cga<tm1Sac>/Cga<tm1Sac>	involves: 129S2/SvPas * C57BL/6J	N	7544315
MGI:2662563	F	MP:0001127	small ovary	Cga<tm1Sac>/Cga<tm1Sac>	involves: 129S2/SvPas * C57BL/6J	N	7544315
MGI:2662563	M	MP:0001925	male infertility	Cga<tm1Sac>/Cga<tm1Sac>	involves: 129S2/SvPas * C57BL/6J	N	7544315
MGI:2662563	F	MP:0001928	abnormal ovulation	Cga<tm1Sac>/Cga<tm1Sac>	involves: 129S2/SvPas * C57BL/6J	N	7544315
MGI:2662563	F	MP:0001121	uterus hypoplasia	Cga<tm1Sac>/Cga<tm1Sac>	involves: 129S2/SvPas * C57BL/6J	N	7544315
MGI:2662715	F	MP:0001129	impaired ovarian folliculogenesis	Gja1<tm1Kdr>/Gja1<tm1Kdr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	10208994
MGI:2662715	M	MP:0001147	small testis	Gja1<tm1Kdr>/Gja1<tm1Kdr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	10208994
MGI:2662715	F	MP:0001127	small ovary	Gja1<tm1Kdr>/Gja1<tm1Kdr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	10208994
MGI:2662755	M	MP:0004901	decreased male germ cell number	Gja1<tm1Kdr>/Gja1<tm1Kdr>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	11514348
MGI:2662779	F	MP:0001127	small ovary	Kitl<Sl-pan>/Kitl<Sl-pan>	involves: C3H	N	7683280
MGI:2662779	F	MP:0001129	impaired ovarian folliculogenesis	Kitl<Sl-pan>/Kitl<Sl-pan>	involves: C3H	N	7683280
MGI:2662779	F	MP:0005431	decreased oocyte number	Kitl<Sl-pan>/Kitl<Sl-pan>	involves: C3H	N	7683280
MGI:2662779	M	MP:0004901	decreased male germ cell number	Kitl<Sl-pan>/Kitl<Sl-pan>	involves: C3H	N	7683280
MGI:2662779	F	MP:0001926	female infertility	Kitl<Sl-pan>/Kitl<Sl-pan>	involves: C3H	N	7683280
MGI:2662939	F	MP:0001926	female infertility	Mitf<Mi-Crc>/Mitf<Mi-Crc>	involves: CBA/CaCrc	N	MGI:2662101
MGI:2662939	M	MP:0001925	male infertility	Mitf<Mi-Crc>/Mitf<Mi-Crc>	involves: CBA/CaCrc	N	MGI:2662101
MGI:2663030	F	MP:0001923	reduced female fertility	Parp1<tm1Jmdm>/Parp1<+>,Parp2<tm1Jmdm>/Parp2<tm1Jmdm>	involves: 129S2/SvPas * C57BL/6	N	12727891
MGI:2663226	F	MP:0001385	pup cannibalization	cir/cir	involves: ICR	N	11924819
MGI:2663242	M	MP:0004901	decreased male germ cell number	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	12432070
MGI:2663242	M	MP:0002685	abnormal spermatogonia proliferation	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	12432070
MGI:2663242	M	MP:0014052	increased male germ cell apoptosis	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	12432070
MGI:2663265	M	MP:0001925	male infertility	Prkaca<tm1Gsm>/Prkaca<tm1Gsm>	involves: 129X1/SvJ * C57BL/6	N	11886853
MGI:2663265	M	MP:0002675	asthenozoospermia	Prkaca<tm1Gsm>/Prkaca<tm1Gsm>	involves: 129X1/SvJ * C57BL/6	N	11875122
MGI:2663270	M	MP:0001922	reduced male fertility	cl/cl	Not Specified	N	MGI:48832
MGI:2663270	F	MP:0001923	reduced female fertility	cl/cl	Not Specified	N	MGI:48832
MGI:2663275	M	MP:0001147	small testis	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	9882500
MGI:2663275	M	MP:0005169	abnormal male meiosis	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	9882500
MGI:2663275	M	MP:0001153	small seminiferous tubules	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	9882500
MGI:2663275	M	MP:0004901	decreased male germ cell number	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	9882500
MGI:2663275	M	MP:0002687	oligozoospermia	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	9882500
MGI:2663275	M	MP:0001932	abnormal spermiogenesis	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	9882500
MGI:2663275	M	MP:0001925	male infertility	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	9882500
MGI:2663351	F	MP:0001399	hyperactivity	Clock<m1Jt>/Clock<m1Jt>	C57BL/6-Clock<m1Jt>	N	12882315
MGI:2663351	F	MP:0002574	increased vertical activity	Clock<m1Jt>/Clock<m1Jt>	C57BL/6-Clock<m1Jt>	N	12882315
MGI:2663361	F	MP:0001386	abnormal maternal nurturing	Lgi4<clp>/Lgi4<clp>	C57BL/6J-Lgi4<clp>/J	N	1652607
MGI:2663361	M	MP:0002566	abnormal sexual interaction	Lgi4<clp>/Lgi4<clp>	C57BL/6J-Lgi4<clp>/J	N	1652607
MGI:2663736	M	MP:0001925	male infertility	Lepr<db-Pas>/Lepr<db-Pas>	involves: DW/Pas	N	3882910
MGI:2663736	F	MP:0001926	female infertility	Lepr<db-Pas>/Lepr<db-Pas>	involves: DW/Pas	N	3882910
MGI:2663744	M	MP:0014052	increased male germ cell apoptosis	Limk2<tm1.1Tnak>/Limk2<tm1.1Tnak>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	11784110
MGI:2663744	M	MP:0004852	decreased testis weight	Limk2<tm1.1Tnak>/Limk2<tm1.1Tnak>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	11784110
MGI:2663744	M	MP:0006379	abnormal spermatocyte morphology	Limk2<tm1.1Tnak>/Limk2<tm1.1Tnak>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	11784110
MGI:2663744	M	MP:0001153	small seminiferous tubules	Limk2<tm1.1Tnak>/Limk2<tm1.1Tnak>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	11784110
MGI:2663744	M	MP:0001156	abnormal spermatogenesis	Limk2<tm1.1Tnak>/Limk2<tm1.1Tnak>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	11784110
MGI:2663772	M	MP:0001147	small testis	Lipe<tm1Ishi>/Lipe<tm1Ishi>	involves: 129S7/SvEvBrd * C57BL/6	N	10639158
MGI:2663772	M	MP:0002687	oligozoospermia	Lipe<tm1Ishi>/Lipe<tm1Ishi>	involves: 129S7/SvEvBrd * C57BL/6	N	10639158
MGI:2663772	M	MP:0001146	abnormal testis morphology	Lipe<tm1Ishi>/Lipe<tm1Ishi>	involves: 129S7/SvEvBrd * C57BL/6	N	10639158
MGI:2663772	M	MP:0002675	asthenozoospermia	Lipe<tm1Ishi>/Lipe<tm1Ishi>	involves: 129S7/SvEvBrd * C57BL/6	N	10639158
MGI:2663772	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Lipe<tm1Ishi>/Lipe<tm1Ishi>	involves: 129S7/SvEvBrd * C57BL/6	N	10639158
MGI:2663772	M	MP:0001925	male infertility	Lipe<tm1Ishi>/Lipe<tm1Ishi>	involves: 129S7/SvEvBrd * C57BL/6	N	10639158
MGI:2663785	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Lipe<tm1Gam>/Lipe<tm1Gam>	involves: 129S4/SvJae	N	11564684
MGI:2663785	M	MP:0005159	azoospermia	Lipe<tm1Gam>/Lipe<tm1Gam>	involves: 129S4/SvJae	N	11564684
MGI:2663785	M	MP:0002631	abnormal epididymis morphology	Lipe<tm1Gam>/Lipe<tm1Gam>	involves: 129S4/SvJae	N	11564684
MGI:2663785	M	MP:0004901	decreased male germ cell number	Lipe<tm1Gam>/Lipe<tm1Gam>	involves: 129S4/SvJae	N	11564684
MGI:2663785	M	MP:0001932	abnormal spermiogenesis	Lipe<tm1Gam>/Lipe<tm1Gam>	involves: 129S4/SvJae	N	11564684
MGI:2663785	M	MP:0004852	decreased testis weight	Lipe<tm1Gam>/Lipe<tm1Gam>	involves: 129S4/SvJae	N	11564684
MGI:2663785	M	MP:0001925	male infertility	Lipe<tm1Gam>/Lipe<tm1Gam>	involves: 129S4/SvJae	N	11564684
MGI:2663785	M	MP:0006380	abnormal spermatid morphology	Lipe<tm1Gam>/Lipe<tm1Gam>	involves: 129S4/SvJae	N	11564684
MGI:2663794	F	MP:0001119	abnormal female reproductive system morphology	Gnrh1<hpg>/Gnrh1<hpg>	involves: 101/H * C3H/HeH	N	198666
MGI:2663794	M	MP:0005188	small penis	Gnrh1<hpg>/Gnrh1<hpg>	involves: 101/H * C3H/HeH	N	198666
MGI:2663794	F	MP:0001129	impaired ovarian folliculogenesis	Gnrh1<hpg>/Gnrh1<hpg>	involves: 101/H * C3H/HeH	N	198666
MGI:2663794	F	MP:0002637	small uterus	Gnrh1<hpg>/Gnrh1<hpg>	involves: 101/H * C3H/HeH	N	198666
MGI:2663794	M	MP:0001157	small seminal vesicle	Gnrh1<hpg>/Gnrh1<hpg>	involves: 101/H * C3H/HeH	N	198666
MGI:2663794	M	MP:0001147	small testis	Gnrh1<hpg>/Gnrh1<hpg>	involves: 101/H * C3H/HeH	N	198666
MGI:2663794	M	MP:0001145	abnormal male reproductive system morphology	Gnrh1<hpg>/Gnrh1<hpg>	involves: 101/H * C3H/HeH	N	198666
MGI:2663794	M	MP:0002669	abnormal scrotum morphology	Gnrh1<hpg>/Gnrh1<hpg>	involves: 101/H * C3H/HeH	N	198666
MGI:2663794	M	MP:0002286	cryptorchism	Gnrh1<hpg>/Gnrh1<hpg>	involves: 101/H * C3H/HeH	N	198666
MGI:2663794	F	MP:0001127	small ovary	Gnrh1<hpg>/Gnrh1<hpg>	involves: 101/H * C3H/HeH	N	198666
MGI:2663794	F	MP:0001142	abnormal vagina orifice morphology	Gnrh1<hpg>/Gnrh1<hpg>	involves: 101/H * C3H/HeH	N	198666
MGI:2663794	M	MP:0008261	arrest of male meiosis	Gnrh1<hpg>/Gnrh1<hpg>	involves: 101/H * C3H/HeH	N	198666
MGI:2663794	M	MP:0002785	absent Leydig cells	Gnrh1<hpg>/Gnrh1<hpg>	involves: 101/H * C3H/HeH	N	19574395
MGI:2663843	M	MP:0002687	oligozoospermia	Man2a2<tm1Mfu>/Man2a2<tm1Mfu>	involves: 129S1/Sv * 129X1/SvJ	N	11778047
MGI:2663843	M	MP:0001147	small testis	Man2a2<tm1Mfu>/Man2a2<tm1Mfu>	involves: 129S1/Sv * 129X1/SvJ	N	12417422
MGI:2663843	M	MP:0001156	abnormal spermatogenesis	Man2a2<tm1Mfu>/Man2a2<tm1Mfu>	involves: 129S1/Sv * 129X1/SvJ	N	11778047
MGI:2663843	M	MP:0001925	male infertility	Man2a2<tm1Mfu>/Man2a2<tm1Mfu>	involves: 129S1/Sv * 129X1/SvJ	N	12417422
MGI:2663843	M	MP:0001147	small testis	Man2a2<tm1Mfu>/Man2a2<tm1Mfu>	involves: 129S1/Sv * 129X1/SvJ	N	11778047
MGI:2663843	M	MP:0001925	male infertility	Man2a2<tm1Mfu>/Man2a2<tm1Mfu>	involves: 129S1/Sv * 129X1/SvJ	N	11778047
MGI:2663843	M	MP:0002687	oligozoospermia	Man2a2<tm1Mfu>/Man2a2<tm1Mfu>	involves: 129S1/Sv * 129X1/SvJ	N	12417422
MGI:2663843	M	MP:0001156	abnormal spermatogenesis	Man2a2<tm1Mfu>/Man2a2<tm1Mfu>	involves: 129S1/Sv * 129X1/SvJ	N	12417422
MGI:2663855	F	MP:0001926	female infertility	Nlrp5<tm1Zbt>/Nlrp5<tm1Zbt>	Not Specified	N	11062459
MGI:2663863	M	MP:0008261	arrest of male meiosis	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	N	8674118
MGI:2663863	F	MP:0001926	female infertility	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	N	8674118
MGI:2663863	M	MP:0001925	male infertility	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	N	8674118
MGI:2663863	M	MP:0001147	small testis	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	N	8674118
MGI:2663863	F	MP:0005168	abnormal female meiosis	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	N	8674118
MGI:2663863	M	MP:0005159	azoospermia	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	N	8674118
MGI:2663872	F	MP:0001127	small ovary	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	N	8673133
MGI:2663872	M	MP:0001925	male infertility	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	N	8673133
MGI:2663872	M	MP:0008261	arrest of male meiosis	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	N	8673133
MGI:2663872	M	MP:0005159	azoospermia	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	N	8673133
MGI:2663872	F	MP:0001926	female infertility	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	N	8673133
MGI:2663872	F	MP:0001130	abnormal ovarian folliculogenesis	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	N	8673133
MGI:2663872	F	MP:0002680	decreased corpora lutea number	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	N	8673133
MGI:2663888	M	MP:0001925	male infertility	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas * C57BL/6	N	7628019
MGI:2663888	M	MP:0002687	oligozoospermia	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas * C57BL/6	N	7628019
MGI:2663888	M	MP:0008892	abnormal sperm flagellum morphology	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas * C57BL/6	N	7628019
MGI:2663888	M	MP:0002686	globozoospermia	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas * C57BL/6	N	7628019
MGI:2663888	M	MP:0005169	abnormal male meiosis	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas * C57BL/6	N	7628019
MGI:2663891	M	MP:0001147	small testis	Mlh3<tm1Lpkn>/Mlh3<tm1Lpkn>	involves: 129S/SvEv	N	12091911
MGI:2663891	M	MP:0005169	abnormal male meiosis	Mlh3<tm1Lpkn>/Mlh3<tm1Lpkn>	involves: 129S/SvEv	N	12091911
MGI:2663891	M	MP:0005159	azoospermia	Mlh3<tm1Lpkn>/Mlh3<tm1Lpkn>	involves: 129S/SvEv	N	12091911
MGI:2663891	F	MP:0001926	female infertility	Mlh3<tm1Lpkn>/Mlh3<tm1Lpkn>	involves: 129S/SvEv	N	12091911
MGI:2663891	M	MP:0001925	male infertility	Mlh3<tm1Lpkn>/Mlh3<tm1Lpkn>	involves: 129S/SvEv	N	12091911
MGI:2663891	F	MP:0005168	abnormal female meiosis	Mlh3<tm1Lpkn>/Mlh3<tm1Lpkn>	involves: 129S/SvEv	N	12091911
MGI:2663909	F	MP:0001935	decreased litter size	Irs4<tm1Lhd>/Irs4<tm1Lhd>	involves: 129S4/SvJae * BALB/c	N	10644546
MGI:2663909	F	MP:0002161	abnormal fertility/fecundity	Irs4<tm1Lhd>/Irs4<tm1Lhd>	involves: 129S4/SvJae * BALB/c	N	10644546
MGI:2663922	F	MP:0001926	female infertility	Mos<tm1Sia>/Mos<tm1Sia>	involves: C57BL/6 * CBA	N	8015610
MGI:2663922	F	MP:0005168	abnormal female meiosis	Mos<tm1Sia>/Mos<tm1Sia>	involves: C57BL/6 * CBA	N	8015610
MGI:2663922	F	MP:0001923	reduced female fertility	Mos<tm1Sia>/Mos<tm1Sia>	involves: C57BL/6 * CBA	N	8015610
MGI:2663946	F	MP:0001127	small ovary	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	N	10809667
MGI:2663946	F	MP:0005168	abnormal female meiosis	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	N	10809667
MGI:2663946	F	MP:0001926	female infertility	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	N	10809667
MGI:2663946	M	MP:0001925	male infertility	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	N	10809667
MGI:2663946	M	MP:0005159	azoospermia	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	N	10809667
MGI:2663946	M	MP:0004852	decreased testis weight	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	N	10809667
MGI:2663946	M	MP:0005169	abnormal male meiosis	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	N	10809667
MGI:2663948	M	MP:0001925	male infertility	Msh4<tm1Wed>/Msh4<tm1Wed>,Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6 * SJL	N	10809667
MGI:2663948	M	MP:0005169	abnormal male meiosis	Msh4<tm1Wed>/Msh4<tm1Wed>,Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6 * SJL	N	10809667
MGI:2663948	F	MP:0001926	female infertility	Msh4<tm1Wed>/Msh4<tm1Wed>,Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6 * SJL	N	10809667
MGI:2664000	M	MP:0006379	abnormal spermatocyte morphology	Fkbp6<tm1Pngr>/Fkbp6<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6	N	12764197
MGI:2664000	M	MP:0008261	arrest of male meiosis	Fkbp6<tm1Pngr>/Fkbp6<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6	N	12764197
MGI:2664000	M	MP:0005159	azoospermia	Fkbp6<tm1Pngr>/Fkbp6<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6	N	12764197
MGI:2664000	M	MP:0001147	small testis	Fkbp6<tm1Pngr>/Fkbp6<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6	N	12764197
MGI:2664000	M	MP:0001925	male infertility	Fkbp6<tm1Pngr>/Fkbp6<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6	N	12764197
MGI:2664131	M	MP:0008261	arrest of male meiosis	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6	N	10678170
MGI:2664131	M	MP:0001153	small seminiferous tubules	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6	N	10678170
MGI:2664131	M	MP:0005159	azoospermia	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6	N	10678170
MGI:2664131	M	MP:0004852	decreased testis weight	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6	N	10678170
MGI:2664131	M	MP:0001925	male infertility	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6	N	10678170
MGI:2664131	M	MP:0006379	abnormal spermatocyte morphology	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6	N	10678170
MGI:2664140	F	MP:0005168	abnormal female meiosis	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6NCrl	N	12004129
MGI:2664140	F	MP:0001923	reduced female fertility	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6NCrl	N	12004129
MGI:2664158	F	MP:0001926	female infertility	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	N	10072381
MGI:2664158	F	MP:0005168	abnormal female meiosis	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	N	10072381
MGI:2664158	F	MP:0012411	increased granulosa cell tumor incidence	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	N	21915857
MGI:2664158	M	MP:0005159	azoospermia	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	N	10072381
MGI:2664158	F	MP:0001127	small ovary	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	N	10072381
MGI:2664158	M	MP:0001925	male infertility	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	N	10072381
MGI:2664158	F	MP:0004805	absent oocytes	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	N	10072381
MGI:2664158	M	MP:0008261	arrest of male meiosis	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	N	10072381
MGI:2664158	F	MP:0002777	absent ovarian follicles	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	N	10072381
MGI:2664158	M	MP:0004852	decreased testis weight	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	N	10072381
MGI:2664158	M	MP:0014052	increased male germ cell apoptosis	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	N	10072381
MGI:2664240	M	MP:0001153	small seminiferous tubules	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	M	MP:0002784	abnormal Sertoli cell morphology	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	M	MP:0008261	arrest of male meiosis	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	M	MP:0008261	arrest of male meiosis	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	21750041
MGI:2664240	F	MP:0006270	abnormal mammary gland growth during lactation	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	M	MP:0005159	azoospermia	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	21750041
MGI:2664240	M	MP:0005159	azoospermia	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	M	MP:0004901	decreased male germ cell number	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	M	MP:0014052	increased male germ cell apoptosis	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	M	MP:0001155	arrest of spermatogenesis	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	F	MP:0009504	abnormal mammary gland epithelium morphology	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	F	MP:0001382	abnormal nursing	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	M	MP:0004852	decreased testis weight	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	M	MP:0001147	small testis	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	M	MP:0006379	abnormal spermatocyte morphology	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	M	MP:0001925	male infertility	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	21750041
MGI:2664240	F	MP:0006269	abnormal mammary gland growth during pregnancy	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664240	M	MP:0001925	male infertility	Mybl1<tm1Epr>/Mybl1<tm1Epr>	Not Specified	N	9109487
MGI:2664262	M	MP:0001156	abnormal spermatogenesis	Slc12a2<tm1Bhk>/Slc12a2<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664262	F	MP:0001923	reduced female fertility	Slc12a2<tm1Bhk>/Slc12a2<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664262	M	MP:0006380	abnormal spermatid morphology	Slc12a2<tm1Bhk>/Slc12a2<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664262	M	MP:0001925	male infertility	Slc12a2<tm1Bhk>/Slc12a2<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664262	M	MP:0001147	small testis	Slc12a2<tm1Bhk>/Slc12a2<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664262	M	MP:0005159	azoospermia	Slc12a2<tm1Bhk>/Slc12a2<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664262	M	MP:0004901	decreased male germ cell number	Slc12a2<tm1Bhk>/Slc12a2<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664262	M	MP:0001380	reduced male mating frequency	Slc12a2<tm1Bhk>/Slc12a2<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664279	M	MP:0001380	reduced male mating frequency	Slc12a2<tm2Bhk>/Slc12a2<tm2Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664279	M	MP:0001156	abnormal spermatogenesis	Slc12a2<tm2Bhk>/Slc12a2<tm2Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664279	M	MP:0001147	small testis	Slc12a2<tm2Bhk>/Slc12a2<tm2Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664279	M	MP:0001925	male infertility	Slc12a2<tm2Bhk>/Slc12a2<tm2Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664279	M	MP:0006380	abnormal spermatid morphology	Slc12a2<tm2Bhk>/Slc12a2<tm2Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664279	F	MP:0001923	reduced female fertility	Slc12a2<tm2Bhk>/Slc12a2<tm2Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664279	M	MP:0005159	azoospermia	Slc12a2<tm2Bhk>/Slc12a2<tm2Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664279	F	MP:0001386	abnormal maternal nurturing	Slc12a2<tm2Bhk>/Slc12a2<tm2Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664279	M	MP:0004901	decreased male germ cell number	Slc12a2<tm2Bhk>/Slc12a2<tm2Bhk>	involves: 129P2/OlaHsd * C57BL/6J * DBA/2J	N	10683373
MGI:2664331	F	MP:0001134	absent corpus luteum	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	F	MP:0001923	reduced female fertility	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	F	MP:0031420	decreased superovulation rate	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	15465527
MGI:2664331	M	MP:0001380	reduced male mating frequency	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	M	MP:0001156	abnormal spermatogenesis	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	F	MP:0001376	abnormal mating receptivity	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	15465527
MGI:2664331	F	MP:0001127	small ovary	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	M	MP:0001147	small testis	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	M	MP:0001925	male infertility	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	F	MP:0001923	reduced female fertility	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	15465527
MGI:2664331	M	MP:0002059	abnormal seminal vesicle morphology	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	M	MP:0001154	seminiferous tubule degeneration	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	F	MP:0001927	abnormal estrous cycle	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	15465527
MGI:2664331	M	MP:0031287	bilateral cryptorchism	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	M	MP:0005159	azoospermia	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	M	MP:0002716	small male preputial gland	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	F	MP:0009014	prolonged proestrus	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	15465527
MGI:2664331	M	MP:0005188	small penis	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	M	MP:0004930	small epididymis	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	F	MP:0009018	short estrus	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	15465527
MGI:2664331	F	MP:0002637	small uterus	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	M	MP:0005536	decreased Leydig cell number	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	M	MP:0002769	abnormal vas deferens morphology	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	M	MP:0004901	decreased male germ cell number	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	M	MP:0001153	small seminiferous tubules	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	F	MP:0001129	impaired ovarian folliculogenesis	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	9090387
MGI:2664331	F	MP:0009011	prolonged diestrus	Nhlh2<tm1Irk>/Nhlh2<tm1Irk>	involves: 129S4/SvJae * C57BL/6	N	15465527
MGI:2664356	F	MP:0001385	pup cannibalization	Col5a2<tm1Rmz>/Col5a2<tm1Rmz>	either: (involves: 129S4/SvJae * 129T2/SvEms) or (involves: 129S4/SvJae * C57BL/6)	N	7704020
MGI:2664362	M	MP:0002631	abnormal epididymis morphology	Ros1<tm1Cbm>/Ros1<tm1Cbm>	involves: 129P2/OlaHsd	N	8675006
MGI:2664362	M	MP:0009248	small caput epididymis	Ros1<tm1Cbm>/Ros1<tm1Cbm>	involves: 129P2/OlaHsd	N	8675006
MGI:2664362	F	MP:0005389	reproductive system phenotype	Ros1<tm1Cbm>/Ros1<tm1Cbm>	involves: 129P2/OlaHsd	Y	8675006
MGI:2664362	M	MP:0002660	abnormal caput epididymis morphology	Ros1<tm1Cbm>/Ros1<tm1Cbm>	involves: 129P2/OlaHsd	N	8675006
MGI:2664362	M	MP:0001925	male infertility	Ros1<tm1Cbm>/Ros1<tm1Cbm>	involves: 129P2/OlaHsd	N	8675006
MGI:2664362	M	MP:0031012	impaired sperm migration in female genital tract	Ros1<tm1Cbm>/Ros1<tm1Cbm>	involves: 129P2/OlaHsd	N	8675006
MGI:2664362	M	MP:0004933	abnormal epididymis epithelium morphology	Ros1<tm1Cbm>/Ros1<tm1Cbm>	involves: 129P2/OlaHsd	N	8675006
MGI:2664397	M	MP:0001925	male infertility	Ros1<tm2Cbm>/Ros1<tm2Cbm>	involves: 129P2/OlaHsd	N	8675006
MGI:2664397	F	MP:0005389	reproductive system phenotype	Ros1<tm2Cbm>/Ros1<tm2Cbm>	involves: 129P2/OlaHsd	Y	8675006
MGI:2664397	M	MP:0004933	abnormal epididymis epithelium morphology	Ros1<tm2Cbm>/Ros1<tm2Cbm>	involves: 129P2/OlaHsd	N	8675006
MGI:2664397	M	MP:0002660	abnormal caput epididymis morphology	Ros1<tm2Cbm>/Ros1<tm2Cbm>	involves: 129P2/OlaHsd	N	8675006
MGI:2664397	M	MP:0002631	abnormal epididymis morphology	Ros1<tm2Cbm>/Ros1<tm2Cbm>	involves: 129P2/OlaHsd	N	8675006
MGI:2664397	M	MP:0009248	small caput epididymis	Ros1<tm2Cbm>/Ros1<tm2Cbm>	involves: 129P2/OlaHsd	N	8675006
MGI:2664397	M	MP:0031012	impaired sperm migration in female genital tract	Ros1<tm2Cbm>/Ros1<tm2Cbm>	involves: 129P2/OlaHsd	N	8675006
MGI:2664516	M	MP:0001167	prostate gland epithelial hyperplasia	Serpinf1<tm1Craw>/Serpinf1<tm1Craw>	involves: 129X1/SvJ * C57BL/6J	N	12740569
MGI:2664516	M	MP:0001158	abnormal prostate gland morphology	Serpinf1<tm1Craw>/Serpinf1<tm1Craw>	involves: 129X1/SvJ * C57BL/6J	N	12740569
MGI:2664519	F	MP:0001926	female infertility	Hoxa10<tm1Rilm>/Hoxa10<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	7700356
MGI:2664519	M	MP:0001922	reduced male fertility	Hoxa10<tm1Rilm>/Hoxa10<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	7700356
MGI:2664519	M	MP:0005159	azoospermia	Hoxa10<tm1Rilm>/Hoxa10<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	7700356
MGI:2664519	M	MP:0000664	small prostate gland anterior lobe	Hoxa10<tm1Rilm>/Hoxa10<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	9915571
MGI:2664519	M	MP:0001147	small testis	Hoxa10<tm1Rilm>/Hoxa10<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	7700356
MGI:2664519	M	MP:0001925	male infertility	Hoxa10<tm1Rilm>/Hoxa10<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	7700356
MGI:2664519	M	MP:0001163	abnormal prostate gland anterior lobe morphology	Hoxa10<tm1Rilm>/Hoxa10<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	9915571
MGI:2664519	M	MP:0000665	decreased ductal branching in the coagulating gland	Hoxa10<tm1Rilm>/Hoxa10<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	9915571
MGI:2664519	M	MP:0013317	abnormal seminal vesicle development	Hoxa10<tm1Rilm>/Hoxa10<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	9915571
MGI:2664519	M	MP:0001153	small seminiferous tubules	Hoxa10<tm1Rilm>/Hoxa10<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	7700356
MGI:2664519	M	MP:0002769	abnormal vas deferens morphology	Hoxa10<tm1Rilm>/Hoxa10<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	9915571
MGI:2664519	M	MP:0031287	bilateral cryptorchism	Hoxa10<tm1Rilm>/Hoxa10<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	7700356
MGI:2664519	M	MP:0001156	abnormal spermatogenesis	Hoxa10<tm1Rilm>/Hoxa10<tm1Rilm>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	N	7700356
MGI:2664581	M	MP:0001925	male infertility	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	F	MP:0009444	ovarian follicular cyst	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8248223
MGI:2664581	F	MP:0001120	abnormal uterus morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	11311804
MGI:2664581	F	MP:0004896	abnormal endometrium morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	11311804
MGI:2664581	F	MP:0001126	abnormal ovary morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8248223
MGI:2664581	F	MP:0001134	absent corpus luteum	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8248223
MGI:2664581	M	MP:0001154	seminiferous tubule degeneration	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	M	MP:0005578	teratozoospermia	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	M	MP:0006423	dilated rete testis	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	F	MP:0004905	decreased uterus weight	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	10558910
MGI:2664581	M	MP:0000242	impaired fertilization	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	M	MP:0005656	decreased aggression	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	9037078
MGI:2664581	M	MP:0009257	dilated seminiferous tubule	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	M	MP:0009856	failure of ejaculation	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	11114183
MGI:2664581	M	MP:0009856	failure of ejaculation	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	9037078
MGI:2664581	M	MP:0001922	reduced male fertility	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8248223
MGI:2664581	M	MP:0001399	hyperactivity	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	9037078
MGI:2664581	F	MP:0003699	abnormal female reproductive system physiology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8248223
MGI:2664581	F	MP:0001385	pup cannibalization	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	9832446
MGI:2664581	F	MP:0001926	female infertility	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8248223
MGI:2664581	F	MP:0001386	abnormal maternal nurturing	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	9832446
MGI:2664581	M	MP:0002631	abnormal epididymis morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	M	MP:0002574	increased vertical activity	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	9037078
MGI:2664581	M	MP:0002675	asthenozoospermia	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	F	MP:0001384	abnormal pup retrieval	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	9832446
MGI:2664581	F	MP:0002637	small uterus	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	11311804
MGI:2664581	M	MP:0001156	abnormal spermatogenesis	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	F	MP:0001356	increased aggression towards female mice	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	9832446
MGI:2664581	M	MP:0001380	reduced male mating frequency	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	9832446
MGI:2664581	M	MP:0001380	reduced male mating frequency	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	9037078
MGI:2664581	M	MP:0001380	reduced male mating frequency	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	F	MP:0001376	abnormal mating receptivity	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	9832446
MGI:2664581	F	MP:0001376	abnormal mating receptivity	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8248223
MGI:2664581	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	M	MP:0008893	detached sperm flagellum	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	M	MP:0004852	decreased testis weight	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8248223
MGI:2664581	M	MP:0004852	decreased testis weight	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	F	MP:0001121	uterus hypoplasia	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8248223
MGI:2664581	M	MP:0002687	oligozoospermia	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664581	M	MP:0002687	oligozoospermia	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8248223
MGI:2664581	M	MP:0002216	abnormal seminiferous tubule morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	N	8895349
MGI:2664687	F	MP:0001126	abnormal ovary morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd	N	10600740
MGI:2664687	F	MP:0001134	absent corpus luteum	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd	N	10600740
MGI:2664687	F	MP:0001121	uterus hypoplasia	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd	N	10600740
MGI:2664687	M	MP:0002687	oligozoospermia	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd	N	10600740
MGI:2664687	F	MP:0001926	female infertility	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd	N	10600740
MGI:2664687	M	MP:0002675	asthenozoospermia	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd	N	10600740
MGI:2664687	M	MP:0001925	male infertility	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd	N	10600740
MGI:2664765	M	MP:0001922	reduced male fertility	Pin1<tm1Tuc>/Pin1<tm1Tuc>	B6.129P2-Pin1<tm1Tuc>	N	12810604
MGI:2664765	F	MP:0008871	abnormal ovarian follicle number	Pin1<tm1Tuc>/Pin1<tm1Tuc>	B6.129P2-Pin1<tm1Tuc>	N	12810604
MGI:2664765	F	MP:0001923	reduced female fertility	Pin1<tm1Tuc>/Pin1<tm1Tuc>	B6.129P2-Pin1<tm1Tuc>	N	12810604
MGI:2664866	M	MP:0002216	abnormal seminiferous tubule morphology	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	N	7569956
MGI:2664866	M	MP:0014052	increased male germ cell apoptosis	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	N	7569956
MGI:2664866	M	MP:0001925	male infertility	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	N	7569956
MGI:2664866	F	MP:0031239	increased atretic ovarian follicle number	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	N	7569956
MGI:2664866	M	MP:0001155	arrest of spermatogenesis	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	N	7569956
MGI:2664866	M	MP:0005159	azoospermia	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	N	7569956
MGI:2664906	M	MP:0001925	male infertility	Tg(Hoxd9/lacZ/neo)5Ddu/Tg(Hoxd9/lacZ/neo)5Ddu	involves: 129S2/SvPas	N	12679098
MGI:2664908	M	MP:0001925	male infertility	Tg(Hoxd9/lacZ/neo)2Ddu/Tg(Hoxd9/lacZ/neo)2Ddu	involves: 129S2/SvPas	N	12679098
MGI:2664909	M	MP:0001925	male infertility	Tg(Hoxd9/lacZ/neo)3Ddu/Tg(Hoxd9/lacZ/neo)3Ddu	involves: 129S2/SvPas	N	12679098
MGI:2664911	M	MP:0001925	male infertility	Tg(Hoxd9/lacZ/neo)4Ddu/Tg(Hoxd9/lacZ/neo)4Ddu	involves: 129S2/SvPas	N	12679098
MGI:2664912	M	MP:0001922	reduced male fertility	Bcl6<tm1Htno>/Bcl6<tm1Htno>	involves: 129S1/Sv * 129X1/SvJ	N	11092811
MGI:2664912	M	MP:0014052	increased male germ cell apoptosis	Bcl6<tm1Htno>/Bcl6<tm1Htno>	involves: 129S1/Sv * 129X1/SvJ	N	11092811
MGI:2664912	M	MP:0009647	decreased fertilization frequency	Bcl6<tm1Htno>/Bcl6<tm1Htno>	involves: 129S1/Sv * 129X1/SvJ	N	11092811
MGI:2664912	M	MP:0002687	oligozoospermia	Bcl6<tm1Htno>/Bcl6<tm1Htno>	involves: 129S1/Sv * 129X1/SvJ	N	11092811
MGI:2664952	F	MP:0013507	increased ovary apoptosis	Figla<tm1Dean>/Figla<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	32086523
MGI:2664952	F	MP:0005431	decreased oocyte number	Figla<tm1Dean>/Figla<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11023867
MGI:2664952	F	MP:0010767	abnormal female meiosis I arrest	Figla<tm1Dean>/Figla<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	32086523
MGI:2664952	F	MP:0005168	abnormal female meiosis	Figla<tm1Dean>/Figla<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	32086523
MGI:2664952	F	MP:0031474	increased female germ cell apoptosis	Figla<tm1Dean>/Figla<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	32086523
MGI:2664952	F	MP:0011122	absent primordial ovarian follicles	Figla<tm1Dean>/Figla<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11023867
MGI:2664952	M	MP:0005389	reproductive system phenotype	Figla<tm1Dean>/Figla<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	11023867
MGI:2664952	F	MP:0001926	female infertility	Figla<tm1Dean>/Figla<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11023867
MGI:2664952	F	MP:0010948	abnormal double-strand DNA break repair	Figla<tm1Dean>/Figla<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	32086523
MGI:2664952	F	MP:0001127	small ovary	Figla<tm1Dean>/Figla<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11023867
MGI:2664952	F	MP:0001931	abnormal oogenesis	Figla<tm1Dean>/Figla<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	32086523
MGI:2664952	F	MP:0001130	abnormal ovarian folliculogenesis	Figla<tm1Dean>/Figla<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11023867
MGI:2665040	M	MP:0004852	decreased testis weight	Fshb<tm1Zuk>/Fshb<tm1Zuk>	involves: 129S7/SvEvBrd	N	11416011
MGI:2665040	M	MP:0006380	abnormal spermatid morphology	Fshb<tm1Zuk>/Fshb<tm1Zuk>	involves: 129S7/SvEvBrd	N	11416011
MGI:2665040	M	MP:0004901	decreased male germ cell number	Fshb<tm1Zuk>/Fshb<tm1Zuk>	involves: 129S7/SvEvBrd	N	11416011
MGI:2665040	M	MP:0001156	abnormal spermatogenesis	Fshb<tm1Zuk>/Fshb<tm1Zuk>	involves: 129S7/SvEvBrd	N	11416011
MGI:2665040	M	MP:0002784	abnormal Sertoli cell morphology	Fshb<tm1Zuk>/Fshb<tm1Zuk>	involves: 129S7/SvEvBrd	N	11416011
MGI:2665040	M	MP:0006378	abnormal spermatogonia morphology	Fshb<tm1Zuk>/Fshb<tm1Zuk>	involves: 129S7/SvEvBrd	N	11416011
MGI:2665042	M	MP:0006380	abnormal spermatid morphology	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	involves: 129S7/SvEvBrd	N	11416011
MGI:2665042	M	MP:0006378	abnormal spermatogonia morphology	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	involves: 129S7/SvEvBrd	N	11416011
MGI:2665042	M	MP:0002784	abnormal Sertoli cell morphology	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	involves: 129S7/SvEvBrd	N	11416011
MGI:2665042	M	MP:0004852	decreased testis weight	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	involves: 129S7/SvEvBrd	N	11416011
MGI:2665042	M	MP:0004901	decreased male germ cell number	Acvr2a<tm1Zuk>/Acvr2a<tm1Zuk>	involves: 129S7/SvEvBrd	N	11416011
MGI:2665094	F	MP:0001127	small ovary	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	M	MP:0004852	decreased testis weight	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	F	MP:0001129	impaired ovarian folliculogenesis	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	M	MP:0002782	abnormal testes secretion	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	F	MP:0001144	vagina atresia	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	F	MP:0009009	absent estrous cycle	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	F	MP:0004905	decreased uterus weight	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	F	MP:0004856	decreased ovary weight	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	F	MP:0001132	absent mature ovarian follicles	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	F	MP:0014270	decreased ovary secretion	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	M	MP:0001153	small seminiferous tubules	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	F	MP:0001134	absent corpus luteum	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	F	MP:0001126	abnormal ovary morphology	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	F	MP:0001926	female infertility	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665094	F	MP:0004894	uterus atrophy	Fshr<tm1Mha>/Fshr<tm1Mha>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10803590
MGI:2665277	M	MP:0004929	decreased epididymis weight	Mark2<Gt(pSABetageo)38Bss>/Mark2<Gt(pSABetageo)38Bss>	involves: 129S2/SvPas * MF1	N	10491259
MGI:2665277	F	MP:0001923	reduced female fertility	Mark2<Gt(pSABetageo)38Bss>/Mark2<Gt(pSABetageo)38Bss>	involves: 129S2/SvPas * MF1	N	10491259
MGI:2665277	F	MP:0002680	decreased corpora lutea number	Mark2<Gt(pSABetageo)38Bss>/Mark2<Gt(pSABetageo)38Bss>	involves: 129S2/SvPas * MF1	N	10491259
MGI:2665277	M	MP:0004910	decreased seminal vesicle weight	Mark2<Gt(pSABetageo)38Bss>/Mark2<Gt(pSABetageo)38Bss>	involves: 129S2/SvPas * MF1	N	10491259
MGI:2665277	F	MP:0004905	decreased uterus weight	Mark2<Gt(pSABetageo)38Bss>/Mark2<Gt(pSABetageo)38Bss>	involves: 129S2/SvPas * MF1	N	10491259
MGI:2665277	M	MP:0004852	decreased testis weight	Mark2<Gt(pSABetageo)38Bss>/Mark2<Gt(pSABetageo)38Bss>	involves: 129S2/SvPas * MF1	N	10491259
MGI:2665277	F	MP:0004856	decreased ovary weight	Mark2<Gt(pSABetageo)38Bss>/Mark2<Gt(pSABetageo)38Bss>	involves: 129S2/SvPas * MF1	N	10491259
MGI:2665287	M	MP:0001925	male infertility	Adam3<tm1Ihgg>/Adam3<tm1Ihgg>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	10569988
MGI:2665287	M	MP:0030978	impaired binding of sperm to zona pellucida	Adam3<tm1Ihgg>/Adam3<tm1Ihgg>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	10569988
MGI:2665309	M	MP:0001925	male infertility	Adam3<tm1Pmkf>/Adam3<tm1Pmkf>	Not Specified	N	11319869
MGI:2665309	M	MP:0030978	impaired binding of sperm to zona pellucida	Adam3<tm1Pmkf>/Adam3<tm1Pmkf>	Not Specified	N	11319869
MGI:2665400	F	MP:0031391	increased locomotor activity	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	involves: 129P2/OlaHsd * C57BL/6J	N	8033209
MGI:2665400	F	MP:0001415	increased exploration in new environment	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	involves: 129P2/OlaHsd * C57BL/6J	N	8033209
MGI:2665401	F	MP:0009937	abnormal neuron differentiation	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	involves: 129P2/OlaHsd	N	20386739
MGI:2665401	F	MP:0004948	abnormal neuronal precursor proliferation	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	involves: 129P2/OlaHsd	N	20386739
MGI:2665401	F	MP:0001488	increased startle reflex	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	involves: 129P2/OlaHsd	N	16055059
MGI:2665401	F	MP:0001898	abnormal long-term depression	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	involves: 129P2/OlaHsd	N	16055059
MGI:2665401	F	MP:0000812	abnormal dentate gyrus morphology	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	involves: 129P2/OlaHsd	N	20386739
MGI:2665401	F	MP:0000877	abnormal Purkinje cell morphology	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	involves: 129P2/OlaHsd	N	16055059
MGI:2665488	F	MP:0001120	abnormal uterus morphology	Pgr<tm1Bwo>/Pgr<tm1Bwo>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7557380
MGI:2665488	F	MP:0003845	abnormal decidualization	Pgr<tm1Bwo>/Pgr<tm1Bwo>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7557380
MGI:2665488	F	MP:0001123	dilated uterus	Pgr<tm1Bwo>/Pgr<tm1Bwo>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7557380
MGI:2665488	F	MP:0001926	female infertility	Pgr<tm1Bwo>/Pgr<tm1Bwo>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7557380
MGI:2665488	F	MP:0000662	abnormal branching of the mammary ductal tree	Pgr<tm1Bwo>/Pgr<tm1Bwo>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7557380
MGI:2665488	F	MP:0031422	failure of superovulation	Pgr<tm1Bwo>/Pgr<tm1Bwo>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7557380
MGI:2665488	F	MP:0008870	increased mature ovarian follicle number	Pgr<tm1Bwo>/Pgr<tm1Bwo>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7557380
MGI:2665488	F	MP:0009251	enlarged endometrial glands	Pgr<tm1Bwo>/Pgr<tm1Bwo>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7557380
MGI:2665488	F	MP:0001376	abnormal mating receptivity	Pgr<tm1Bwo>/Pgr<tm1Bwo>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7557380
MGI:2665488	F	MP:0001134	absent corpus luteum	Pgr<tm1Bwo>/Pgr<tm1Bwo>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7557380
MGI:2665488	F	MP:0000628	abnormal mammary gland development	Pgr<tm1Bwo>/Pgr<tm1Bwo>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7557380
MGI:2665488	F	MP:0003356	impaired luteinization	Pgr<tm1Bwo>/Pgr<tm1Bwo>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7557380
MGI:2665488	F	MP:0002676	uterus hyperplasia	Pgr<tm1Bwo>/Pgr<tm1Bwo>	either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	N	7557380
MGI:2665492	F	MP:0003845	abnormal decidualization	Pgr<tm1Omc>/Pgr<tm1Omc>	involves: 129S7/SvEvBrd * C57BL/6J	N	10976068
MGI:2665492	F	MP:0031420	decreased superovulation rate	Pgr<tm1Omc>/Pgr<tm1Omc>	involves: 129S7/SvEvBrd * C57BL/6J	N	10976068
MGI:2665492	F	MP:0002676	uterus hyperplasia	Pgr<tm1Omc>/Pgr<tm1Omc>	involves: 129S7/SvEvBrd * C57BL/6J	N	10976068
MGI:2665492	F	MP:0004014	abnormal uterine environment	Pgr<tm1Omc>/Pgr<tm1Omc>	involves: 129S7/SvEvBrd * C57BL/6J	N	10976068
MGI:2665492	F	MP:0001926	female infertility	Pgr<tm1Omc>/Pgr<tm1Omc>	involves: 129S7/SvEvBrd * C57BL/6J	N	10976068
MGI:2665504	F	MP:0001554	increased circulating free fatty acids level	Apc<Min>/Apc<+>	C57BL/6J-Apc<Min>	N	14522940
MGI:2665504	F	MP:0001552	increased circulating triglyceride level	Apc<Min>/Apc<+>	C57BL/6J-Apc<Min>	N	14522940
MGI:2665504	M	MP:0001732	postnatal growth retardation	Apc<Min>/Apc<+>	C57BL/6J-Apc<Min>	N	12941845
MGI:2665513	M	MP:0009282	decreased hyperactivated sperm motility	Pcsk4<tm1Mbi>/Pcsk4<tm1Mbi>	involves: 129P2/OlaHsd * C57BL/6J	N	9192653
MGI:2665513	M	MP:0001922	reduced male fertility	Pcsk4<tm1Mbi>/Pcsk4<tm1Mbi>	involves: 129P2/OlaHsd * C57BL/6J	N	9192653
MGI:2665513	F	MP:0001923	reduced female fertility	Pcsk4<tm1Mbi>/Pcsk4<tm1Mbi>	involves: 129P2/OlaHsd * C57BL/6J	N	9192653
MGI:2665553	M	MP:0001146	abnormal testis morphology	Rara<tm1Ipc>/Rara<tm1Ipc>	involves: 129S2/SvPas	N	8394014
MGI:2665553	M	MP:0001925	male infertility	Rara<tm1Ipc>/Rara<tm1Ipc>	involves: 129S2/SvPas	N	8394014
MGI:2665553	M	MP:0001154	seminiferous tubule degeneration	Rara<tm1Ipc>/Rara<tm1Ipc>	involves: 129S2/SvPas	N	8394014
MGI:2665553	M	MP:0002687	oligozoospermia	Rara<tm1Ipc>/Rara<tm1Ipc>	involves: 129S2/SvPas	N	8394014
MGI:2665553	M	MP:0001156	abnormal spermatogenesis	Rara<tm1Ipc>/Rara<tm1Ipc>	involves: 129S2/SvPas	N	8394014
MGI:2665559	F	MP:0001926	female infertility	Ttpa<tm1Hsz>/Ttpa<tm1Hsz>	involves: 129S7/SvEvBrd * C57BL/6J	N	11076932
MGI:2665708	M	MP:0001925	male infertility	Rarg<tm1Ipc>/Rarg<tm1Ipc>	involves: 129S2/SvPas	N	8388780
MGI:2665708	M	MP:0001158	abnormal prostate gland morphology	Rarg<tm1Ipc>/Rarg<tm1Ipc>	involves: 129S2/SvPas	N	8388780
MGI:2665708	M	MP:0013319	seminal vesicle atrophy	Rarg<tm1Ipc>/Rarg<tm1Ipc>	involves: 129S2/SvPas	N	8388780
MGI:2665708	M	MP:0013321	squamous metaplasia of seminal vesicles	Rarg<tm1Ipc>/Rarg<tm1Ipc>	involves: 129S2/SvPas	N	8388780
MGI:2665708	M	MP:0013322	squamous metaplasia of prostate gland	Rarg<tm1Ipc>/Rarg<tm1Ipc>	involves: 129S2/SvPas	N	8388780
MGI:2665776	F	MP:0009081	thin uterus	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0009237	kinked sperm flagellum	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0006378	abnormal spermatogonia morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0002216	abnormal seminiferous tubule morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0002687	oligozoospermia	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0001932	abnormal spermiogenesis	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0009233	enlarged sperm head	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	F	MP:0001132	absent mature ovarian follicles	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0008892	abnormal sperm flagellum morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0001157	small seminal vesicle	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0001157	small seminal vesicle	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0001922	reduced male fertility	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0001922	reduced male fertility	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0008892	abnormal sperm flagellum morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	F	MP:0001926	female infertility	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	F	MP:0001127	small ovary	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0006380	abnormal spermatid morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0004543	abnormal sperm physiology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0001147	small testis	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0002631	abnormal epididymis morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	F	MP:0001129	impaired ovarian folliculogenesis	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	F	MP:0008869	anovulation	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0004930	small epididymis	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0004852	decreased testis weight	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0002675	asthenozoospermia	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0002675	asthenozoospermia	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	F	MP:0001130	abnormal ovarian folliculogenesis	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	F	MP:0001134	absent corpus luteum	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0001153	small seminiferous tubules	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0001153	small seminiferous tubules	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	F	MP:0013348	adenohypophysis hyperplasia	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0004929	decreased epididymis weight	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	F	MP:0002637	small uterus	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0004849	abnormal testis size	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0001156	abnormal spermatogenesis	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0001156	abnormal spermatogenesis	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	9811848
MGI:2665776	M	MP:0004910	decreased seminal vesicle weight	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665776	M	MP:0002660	abnormal caput epididymis morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: C57BL/6	N	10775161
MGI:2665793	M	MP:0003557	absent vas deferens	Ar<Tfm>/Y	STOCK Eda<Ta> Atp7a<Mo-blo>/+ +	N	5452809
MGI:2665793	M	MP:0008261	arrest of male meiosis	Ar<Tfm>/Y	STOCK Eda<Ta> Atp7a<Mo-blo>/+ +	N	5452809
MGI:2665793	F	MP:0001119	abnormal female reproductive system morphology	Ar<Tfm>/Y	STOCK Eda<Ta> Atp7a<Mo-blo>/+ +	N	5452809
MGI:2665793	M	MP:0004727	absent epididymis	Ar<Tfm>/Y	STOCK Eda<Ta> Atp7a<Mo-blo>/+ +	N	5452809
MGI:2665793	F	MP:0001144	vagina atresia	Ar<Tfm>/Y	STOCK Eda<Ta> Atp7a<Mo-blo>/+ +	N	5452809
MGI:2665793	M	MP:0001145	abnormal male reproductive system morphology	Ar<Tfm>/Y	STOCK Eda<Ta> Atp7a<Mo-blo>/+ +	N	5452809
MGI:2665793	M	MP:0002286	cryptorchism	Ar<Tfm>/Y	STOCK Eda<Ta> Atp7a<Mo-blo>/+ +	N	5452809
MGI:2665793	M	MP:0001147	small testis	Ar<Tfm>/Y	STOCK Eda<Ta> Atp7a<Mo-blo>/+ +	N	5452809
MGI:2665793	M	MP:0013598	Leydig cell hypertrophy	Ar<Tfm>/Y	STOCK Eda<Ta> Atp7a<Mo-blo>/+ +	N	5452809
MGI:2665799	M	MP:0013604	abnormal adult Leydig cell differentiation	Ar<Tfm>/Y	Not Specified	N	11090455
MGI:2665799	M	MP:0001156	abnormal spermatogenesis	Ar<Tfm>/Y	Not Specified	N	11090455
MGI:2665799	M	MP:0001146	abnormal testis morphology	Ar<Tfm>/Y	Not Specified	N	11090455
MGI:2665799	M	MP:0000968	abnormal sensory neuron innervation pattern	Ar<Tfm>/Y	Not Specified	N	23224557
MGI:2665821	M	MP:0005250	decreased Sertoli cell number	Bcl2l2<Gt(ROSA)41Sor>/Bcl2l2<Gt(ROSA)41Sor>	involves: 129S5/SvEvBrd * C57BL/6J	N	11420255
MGI:2665821	M	MP:0001152	increased Leydig cell number	Bcl2l2<Gt(ROSA)41Sor>/Bcl2l2<Gt(ROSA)41Sor>	involves: 129S5/SvEvBrd * C57BL/6J	N	11420255
MGI:2665821	M	MP:0004910	decreased seminal vesicle weight	Bcl2l2<Gt(ROSA)41Sor>/Bcl2l2<Gt(ROSA)41Sor>	involves: 129S5/SvEvBrd * C57BL/6J	N	11420255
MGI:2665821	M	MP:0004852	decreased testis weight	Bcl2l2<Gt(ROSA)41Sor>/Bcl2l2<Gt(ROSA)41Sor>	involves: 129S5/SvEvBrd * C57BL/6J	N	11420255
MGI:2665821	M	MP:0001153	small seminiferous tubules	Bcl2l2<Gt(ROSA)41Sor>/Bcl2l2<Gt(ROSA)41Sor>	involves: 129S5/SvEvBrd * C57BL/6J	N	11420255
MGI:2665821	M	MP:0002785	absent Leydig cells	Bcl2l2<Gt(ROSA)41Sor>/Bcl2l2<Gt(ROSA)41Sor>	involves: 129S5/SvEvBrd * C57BL/6J	N	11420255
MGI:2665821	M	MP:0020355	abnormal Sertoli cell barrier morphology	Bcl2l2<Gt(ROSA)41Sor>/Bcl2l2<Gt(ROSA)41Sor>	involves: 129S5/SvEvBrd * C57BL/6J	N	11420255
MGI:2667791	M	MP:0005159	azoospermia	Mgat2<tm1.1Jxm>/Mgat2<tm1.1Jxm>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	11805078
MGI:2667791	M	MP:0001925	male infertility	Mgat2<tm1.1Jxm>/Mgat2<tm1.1Jxm>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	11805078
MGI:2667791	M	MP:0001146	abnormal testis morphology	Mgat2<tm1.1Jxm>/Mgat2<tm1.1Jxm>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	11805078
MGI:2667791	M	MP:0008261	arrest of male meiosis	Mgat2<tm1.1Jxm>/Mgat2<tm1.1Jxm>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	11805078
MGI:2667791	F	MP:0001923	reduced female fertility	Mgat2<tm1.1Jxm>/Mgat2<tm1.1Jxm>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	11805078
MGI:2667791	F	MP:0001386	abnormal maternal nurturing	Mgat2<tm1.1Jxm>/Mgat2<tm1.1Jxm>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	11805078
MGI:2668037	M	MP:0002631	abnormal epididymis morphology	Hexa<tm1Grv>/Hexa<tm1Grv>	involves: 129P2/Ola * C57BL/6J	N	9645704
MGI:2668046	M	MP:0009256	enlarged corpus epididymis	Hexb<tm1Grv>/Hexb<tm1Grv>	either: (involves: 129P2/Ola * C57BL/6J) or (involves: 129S1/Sv * 129X1/SvJ * C57L/6J)	N	9645704
MGI:2668046	M	MP:0009249	enlarged caput epididymis	Hexb<tm1Grv>/Hexb<tm1Grv>	either: (involves: 129P2/Ola * C57BL/6J) or (involves: 129S1/Sv * 129X1/SvJ * C57L/6J)	N	9645704
MGI:2668046	M	MP:0002631	abnormal epididymis morphology	Hexb<tm1Grv>/Hexb<tm1Grv>	either: (involves: 129P2/Ola * C57BL/6J) or (involves: 129S1/Sv * 129X1/SvJ * C57L/6J)	N	9645704
MGI:2668046	M	MP:0002566	abnormal sexual interaction	Hexb<tm1Grv>/Hexb<tm1Grv>	either: (involves: 129P2/Ola * C57BL/6J) or (involves: 129S1/Sv * 129X1/SvJ * C57L/6J)	N	12617783
MGI:2668046	M	MP:0004728	abnormal efferent ductules of testis morphology	Hexb<tm1Grv>/Hexb<tm1Grv>	either: (involves: 129P2/Ola * C57BL/6J) or (involves: 129S1/Sv * 129X1/SvJ * C57L/6J)	N	9645704
MGI:2668046	M	MP:0004928	increased epididymis weight	Hexb<tm1Grv>/Hexb<tm1Grv>	either: (involves: 129P2/Ola * C57BL/6J) or (involves: 129S1/Sv * 129X1/SvJ * C57L/6J)	N	9645704
MGI:2668075	M	MP:0008898	abnormal acrosome morphology	Tbpl1<tm1Rgr>/Tbpl1<tm1Rgr>	involves: C57BL/6	N	11352070
MGI:2668075	M	MP:0004852	decreased testis weight	Tbpl1<tm1Rgr>/Tbpl1<tm1Rgr>	involves: C57BL/6	N	11352070
MGI:2668075	M	MP:0006380	abnormal spermatid morphology	Tbpl1<tm1Rgr>/Tbpl1<tm1Rgr>	involves: C57BL/6	N	11352070
MGI:2668075	M	MP:0005159	azoospermia	Tbpl1<tm1Rgr>/Tbpl1<tm1Rgr>	involves: C57BL/6	N	11352070
MGI:2668075	M	MP:0020550	multinucleated giant male germ cells	Tbpl1<tm1Rgr>/Tbpl1<tm1Rgr>	involves: C57BL/6	N	11352070
MGI:2668075	M	MP:0001147	small testis	Tbpl1<tm1Rgr>/Tbpl1<tm1Rgr>	involves: C57BL/6	N	11352070
MGI:2668075	M	MP:0014052	increased male germ cell apoptosis	Tbpl1<tm1Rgr>/Tbpl1<tm1Rgr>	involves: C57BL/6	N	11352070
MGI:2668075	M	MP:0001153	small seminiferous tubules	Tbpl1<tm1Rgr>/Tbpl1<tm1Rgr>	involves: C57BL/6	N	11352070
MGI:2668075	M	MP:0001154	seminiferous tubule degeneration	Tbpl1<tm1Rgr>/Tbpl1<tm1Rgr>	involves: C57BL/6	N	11352070
MGI:2668075	M	MP:0008279	arrest of spermiogenesis	Tbpl1<tm1Rgr>/Tbpl1<tm1Rgr>	involves: C57BL/6	N	11352070
MGI:2668075	M	MP:0002216	abnormal seminiferous tubule morphology	Tbpl1<tm1Rgr>/Tbpl1<tm1Rgr>	involves: C57BL/6	N	11352070
MGI:2668075	M	MP:0001925	male infertility	Tbpl1<tm1Rgr>/Tbpl1<tm1Rgr>	involves: C57BL/6	N	11352070
MGI:2668076	M	MP:0001147	small testis	Tbpl1<tm1Saco>/Tbpl1<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	11463376
MGI:2668076	M	MP:0005159	azoospermia	Tbpl1<tm1Saco>/Tbpl1<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	11463376
MGI:2668076	M	MP:0008279	arrest of spermiogenesis	Tbpl1<tm1Saco>/Tbpl1<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	11463376
MGI:2668076	M	MP:0014052	increased male germ cell apoptosis	Tbpl1<tm1Saco>/Tbpl1<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	11463376
MGI:2668076	M	MP:0002216	abnormal seminiferous tubule morphology	Tbpl1<tm1Saco>/Tbpl1<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	11463376
MGI:2668076	M	MP:0001925	male infertility	Tbpl1<tm1Saco>/Tbpl1<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	11463376
MGI:2668213	M	MP:0001940	testis hypoplasia	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	N	9217007
MGI:2668213	M	MP:0011410	ectopic testis	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	N	9217007
MGI:2668213	F	MP:0009085	abnormal uterine horn morphology	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	N	9217007
MGI:2668214	M	MP:0002687	oligozoospermia	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	N	12220125
MGI:2668214	M	MP:0005304	bulbourethral gland cyst	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	N	12220125
MGI:2668214	M	MP:0001169	abnormal bulbourethral gland morphology	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	N	12220125
MGI:2668214	M	MP:0011781	abnormal bulbourethral gland physiology	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	N	12220125
MGI:2668214	M	MP:0001156	abnormal spermatogenesis	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	N	12220125
MGI:2668214	M	MP:0005305	prostate gland anterior lobe hyperplasia	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	N	12220125
MGI:2668214	M	MP:0001170	bulbourethral gland hyperplasia	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	N	12220125
MGI:2668214	M	MP:0005578	teratozoospermia	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	N	12220125
MGI:2668335	F	MP:0001130	abnormal ovarian folliculogenesis	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>	involves: 129S6/SvEvTac * FVB/N	N	12855809
MGI:2668335	F	MP:0001125	abnormal oocyte morphology	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>	involves: 129S6/SvEvTac * FVB/N	N	12855809
MGI:2668335	F	MP:0008000	increased ovary tumor incidence	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>	involves: 129S6/SvEvTac * FVB/N	N	17254969
MGI:2668335	F	MP:0031239	increased atretic ovarian follicle number	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>	involves: 129S6/SvEvTac * FVB/N	N	12855809
MGI:2668335	F	MP:0009009	absent estrous cycle	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>	involves: 129S6/SvEvTac * FVB/N	N	12855809
MGI:2668335	F	MP:0001927	abnormal estrous cycle	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>	involves: 129S6/SvEvTac * FVB/N	N	12855809
MGI:2668335	F	MP:0004832	enlarged ovary	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>	involves: 129S6/SvEvTac * FVB/N	N	12855809
MGI:2668335	F	MP:0001923	reduced female fertility	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>	involves: 129S6/SvEvTac * FVB/N	N	12855809
MGI:2668460	F	MP:0004514	dystocia	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	9886856
MGI:2668460	M	MP:0001922	reduced male fertility	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	M	MP:0001157	small seminal vesicle	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	M	MP:0001147	small testis	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	M	MP:0001158	abnormal prostate gland morphology	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	M	MP:0001168	abnormal prostate gland epithelium morphology	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	M	MP:0002774	small prostate gland	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	F	MP:0006269	abnormal mammary gland growth during pregnancy	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	9886856
MGI:2668460	M	MP:0002216	abnormal seminiferous tubule morphology	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	F	MP:0006271	abnormal involution of the mammary gland	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	9886856
MGI:2668460	M	MP:0001145	abnormal male reproductive system morphology	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	M	MP:0004930	small epididymis	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	F	MP:0009503	abnormal mammary gland duct morphology	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	9886856
MGI:2668460	M	MP:0001146	abnormal testis morphology	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	M	MP:0002631	abnormal epididymis morphology	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	M	MP:0001156	abnormal spermatogenesis	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	F	MP:0006078	abnormal nipple morphology	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	9886856
MGI:2668460	M	MP:0002687	oligozoospermia	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	M	MP:0001938	delayed sexual maturation	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	F	MP:0006270	abnormal mammary gland growth during lactation	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	9886856
MGI:2668460	M	MP:0009735	abnormal prostate gland development	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	12861045
MGI:2668460	F	MP:0013713	decreased nipple size	Rln1<tm1Wint>/Rln1<tm1Wint>	involves: 129S1/Sv * C57BL/6J	N	9886856
MGI:2668523	F	MP:0002064	seizures	Hprt1<tm2Detl>/Hprt1<tm2Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668523	F	MP:0002066	abnormal motor capabilities/coordination/movement	Hprt1<tm2Detl>/Hprt1<tm2Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668523	F	MP:0004191	neuronal intranuclear inclusions	Hprt1<tm2Detl>/Hprt1<tm2Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668523	F	MP:0002083	premature death	Hprt1<tm2Detl>/Hprt1<tm2Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668523	F	MP:0001402	decreased locomotor activity	Hprt1<tm2Detl>/Hprt1<tm2Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668524	F	MP:0005386	behavior/neurological phenotype	Hprt1<tm3Detl>/Hprt1<tm3Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	12812988
MGI:2668525	F	MP:0002066	abnormal motor capabilities/coordination/movement	Hprt1<tm4Detl>/Hprt1<tm4Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668525	F	MP:0004191	neuronal intranuclear inclusions	Hprt1<tm4Detl>/Hprt1<tm4Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668525	F	MP:0002083	premature death	Hprt1<tm4Detl>/Hprt1<tm4Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668525	F	MP:0001961	abnormal reflex	Hprt1<tm4Detl>/Hprt1<tm4Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668525	F	MP:0002064	seizures	Hprt1<tm4Detl>/Hprt1<tm4Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668525	F	MP:0001402	decreased locomotor activity	Hprt1<tm4Detl>/Hprt1<tm4Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668526	F	MP:0005386	behavior/neurological phenotype	Hprt1<tm5Detl>/Hprt1<tm5Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	12812988
MGI:2668527	F	MP:0002083	premature death	Hprt1<tm6Detl>/Hprt1<tm6Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668527	F	MP:0002066	abnormal motor capabilities/coordination/movement	Hprt1<tm6Detl>/Hprt1<tm6Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668527	F	MP:0004191	neuronal intranuclear inclusions	Hprt1<tm6Detl>/Hprt1<tm6Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668527	F	MP:0002064	seizures	Hprt1<tm6Detl>/Hprt1<tm6Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668527	F	MP:0001402	decreased locomotor activity	Hprt1<tm6Detl>/Hprt1<tm6Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668528	F	MP:0005386	behavior/neurological phenotype	Hprt1<tm7Detl>/Hprt1<tm7Detl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	12812988
MGI:2668531	M	MP:0002083	premature death	Hprt1<tm2Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668531	M	MP:0004191	neuronal intranuclear inclusions	Hprt1<tm2Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668531	M	MP:0001402	decreased locomotor activity	Hprt1<tm2Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668531	M	MP:0002066	abnormal motor capabilities/coordination/movement	Hprt1<tm2Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668531	M	MP:0002064	seizures	Hprt1<tm2Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668532	M	MP:0005386	behavior/neurological phenotype	Hprt1<tm3Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	12812988
MGI:2668533	M	MP:0001402	decreased locomotor activity	Hprt1<tm4Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668533	M	MP:0004191	neuronal intranuclear inclusions	Hprt1<tm4Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668533	M	MP:0002064	seizures	Hprt1<tm4Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668533	M	MP:0002083	premature death	Hprt1<tm4Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668533	M	MP:0002066	abnormal motor capabilities/coordination/movement	Hprt1<tm4Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668533	M	MP:0001961	abnormal reflex	Hprt1<tm4Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668534	M	MP:0005386	behavior/neurological phenotype	Hprt1<tm5Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	12812988
MGI:2668535	M	MP:0002066	abnormal motor capabilities/coordination/movement	Hprt1<tm6Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668535	M	MP:0001402	decreased locomotor activity	Hprt1<tm6Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668535	M	MP:0004191	neuronal intranuclear inclusions	Hprt1<tm6Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668535	M	MP:0002064	seizures	Hprt1<tm6Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668535	M	MP:0002083	premature death	Hprt1<tm6Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12812988
MGI:2668536	M	MP:0005386	behavior/neurological phenotype	Hprt1<tm7Detl>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	12812988
MGI:2668538	M	MP:0001925	male infertility	Hoxd4<tm1Bhr>/Hoxd4<tm1Bhr>,Rarg<tm1Ipc>/Rarg<tm1Ipc>	involves: 129S2/SvPas * 129S7/SvEvBrd * CD-1	N	10559481
MGI:2668732	F	MP:0001923	reduced female fertility	Npm2<tm1Zuk>/Npm2<tm1Zuk>	involves: 129 * C57BL/6J	N	12714744
MGI:2668732	F	MP:0001125	abnormal oocyte morphology	Npm2<tm1Zuk>/Npm2<tm1Zuk>	involves: 129 * C57BL/6J	N	12714744
MGI:2668816	F	MP:0002169	no abnormal phenotype detected	Ocrl<tm1Nbm>/Ocrl<tm1Nbm>	either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * NIH Black Swiss)	N	9593760
MGI:2668817	F	MP:0005389	reproductive system phenotype	Ocrl<tm2Nbm>/Ocrl<tm2Nbm>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * NIH Black Swiss)	Y	9593760
MGI:2668817	F	MP:0005376	homeostasis/metabolism phenotype	Ocrl<tm2Nbm>/Ocrl<tm2Nbm>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * NIH Black Swiss)	Y	9593760
MGI:2668817	F	MP:0005391	vision/eye phenotype	Ocrl<tm2Nbm>/Ocrl<tm2Nbm>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * NIH Black Swiss)	Y	9593760
MGI:2668817	F	MP:0010768	mortality/aging	Ocrl<tm2Nbm>/Ocrl<tm2Nbm>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * NIH Black Swiss)	Y	9593760
MGI:2668818	M	MP:0001925	male infertility	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	9593760
MGI:2668849	M	MP:0001379	abnormal penile erection	Prkg1<tm1Hfm>/Prkg1<tm1Hfm>	Not Specified	N	10688876
MGI:2668849	M	MP:0001922	reduced male fertility	Prkg1<tm1Hfm>/Prkg1<tm1Hfm>	Not Specified	N	10688876
MGI:2668968	M	MP:0008545	absent sperm flagellum	Foxj1<tm1Bph>/Foxj1<tm1Bph>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	9739041
MGI:2668968	F	MP:0011645	absent oviduct epithelium motile cilium	Foxj1<tm1Bph>/Foxj1<tm1Bph>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	9739041
MGI:2669183	M	MP:0004852	decreased testis weight	Nkx2-1<tm1Shk>/Nkx2-1<tm1Shk>	involves: 129S4/SvJae	N	12399445
MGI:2669183	M	MP:0014269	decreased testes secretion	Nkx2-1<tm1Shk>/Nkx2-1<tm1Shk>	involves: 129S4/SvJae	N	12399445
MGI:2669183	M	MP:0002786	abnormal Leydig cell morphology	Nkx2-1<tm1Shk>/Nkx2-1<tm1Shk>	involves: 129S4/SvJae	N	12399445
MGI:2669284	M	MP:0001925	male infertility	Sp4<tm1Ssp>/Sp4<tm1Ssp>	involves: 129P2/OlaHsd * CF-1	N	8660867
MGI:2669284	M	MP:0001380	reduced male mating frequency	Sp4<tm1Ssp>/Sp4<tm1Ssp>	involves: 129P2/OlaHsd * CF-1	N	8660867
MGI:2669401	F	MP:0009503	abnormal mammary gland duct morphology	Cav1<tm1Mls>/Cav1<tm1Mls>	involves: 129/Sv * C57BL/6 * SJL	N	11739396
MGI:2669401	F	MP:0001885	mammary gland duct hyperplasia	Cav1<tm1Mls>/Cav1<tm1Mls>	involves: 129/Sv * C57BL/6 * SJL	N	12368209
MGI:2669401	F	MP:0011939	increased food intake	Cav1<tm1Mls>/Cav1<tm1Mls>	involves: 129/Sv * C57BL/6 * SJL	N	11739396
MGI:2669401	F	MP:0000627	abnormal mammary gland morphology	Cav1<tm1Mls>/Cav1<tm1Mls>	involves: 129/Sv * C57BL/6 * SJL	N	11739396
MGI:2669401	F	MP:0000630	mammary gland hyperplasia	Cav1<tm1Mls>/Cav1<tm1Mls>	involves: 129/Sv * C57BL/6 * SJL	N	12368209
MGI:2669401	F	MP:0009504	abnormal mammary gland epithelium morphology	Cav1<tm1Mls>/Cav1<tm1Mls>	involves: 129/Sv * C57BL/6 * SJL	N	12368209
MGI:2669401	F	MP:0008904	abnormal mammary fat pad morphology	Cav1<tm1Mls>/Cav1<tm1Mls>	involves: 129/Sv * C57BL/6 * SJL	N	11739396
MGI:2669529	F	MP:0000627	abnormal mammary gland morphology	Hr<hr>/Hr<hr>	Not Specified	N	MGI:50932
MGI:2669529	F	MP:0001382	abnormal nursing	Hr<hr>/Hr<hr>	Not Specified	N	MGI:50932
MGI:2669721	F	MP:0005405	axon degeneration	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:2669721	F	MP:0030987	spinal cord inflammation	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:2669721	F	MP:0001405	impaired coordination	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:2669721	F	MP:0008918	microgliosis	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:2669721	F	MP:0001406	abnormal gait	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:2669721	F	MP:0010205	abnormal oligodendrocyte apoptosis	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:2669721	F	MP:0002229	neurodegeneration	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	12805295
MGI:2669721	F	MP:0000951	sporadic seizures	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	12805295
MGI:2669721	F	MP:0000953	abnormal oligodendrocyte morphology	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:2669721	F	MP:0000921	demyelination	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:2669721	F	MP:0000745	tremors	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	12805295
MGI:2669721	F	MP:0000745	tremors	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:2669721	F	MP:0000920	abnormal myelination	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	12805295
MGI:2669721	F	MP:0003354	astrocytosis	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:2669721	F	MP:0002826	tonic seizures	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:2669721	F	MP:0002826	tonic seizures	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	12805295
MGI:2669721	F	MP:0002064	seizures	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	12805295
MGI:2669721	F	MP:0002083	premature death	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:2669721	F	MP:0002083	premature death	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	12805295
MGI:2669721	F	MP:0013438	dysmyelination	Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:2669851	M	MP:0001925	male infertility	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669851	M	MP:0004852	decreased testis weight	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669851	M	MP:0001155	arrest of spermatogenesis	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669851	M	MP:0004901	decreased male germ cell number	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669851	M	MP:0001156	abnormal spermatogenesis	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669851	M	MP:0006379	abnormal spermatocyte morphology	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669851	M	MP:0006380	abnormal spermatid morphology	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669851	M	MP:0020550	multinucleated giant male germ cells	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669854	M	MP:0002673	abnormal sperm number	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669854	M	MP:0020550	multinucleated giant male germ cells	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669854	M	MP:0004901	decreased male germ cell number	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669854	M	MP:0001925	male infertility	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669854	M	MP:0001146	abnormal testis morphology	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669854	M	MP:0004852	decreased testis weight	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669854	M	MP:0001155	arrest of spermatogenesis	Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669856	M	MP:0020550	multinucleated giant male germ cells	Pafah1b1<tm1Awb>/Pafah1b1<+>,Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669856	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Pafah1b1<tm1Awb>/Pafah1b1<+>,Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669856	M	MP:0004852	decreased testis weight	Pafah1b1<tm1Awb>/Pafah1b1<+>,Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2669856	M	MP:0004901	decreased male germ cell number	Pafah1b1<tm1Awb>/Pafah1b1<+>,Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>	involves: 129S6/SvEvTac	N	12775763
MGI:2670462	M	MP:0008261	arrest of male meiosis	Gnpat<tm1Just>/Gnpat<tm1Just>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12874108
MGI:2670462	F	MP:0001127	small ovary	Gnpat<tm1Just>/Gnpat<tm1Just>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12874108
MGI:2670462	M	MP:0001925	male infertility	Gnpat<tm1Just>/Gnpat<tm1Just>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12874108
MGI:2670462	M	MP:0005159	azoospermia	Gnpat<tm1Just>/Gnpat<tm1Just>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12874108
MGI:2670462	M	MP:0002216	abnormal seminiferous tubule morphology	Gnpat<tm1Just>/Gnpat<tm1Just>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12874108
MGI:2670578	F	MP:0001923	reduced female fertility	Pdgfb<tm3.1Cbet>/Pdgfb<tm3.1Cbet>	involves: 129S1/Sv * 129X1/SvJ	N	12897053
MGI:2670731	F	MP:0000373	belly spot	tmgc17/tmgc17	involves: 101/Rl * C3H/HeA * C3H/Rl * C57BL/6JRn * C57/BLiA	N	MGI:2448159
MGI:2670731	F	MP:0000585	kinked tail	tmgc17/tmgc17	involves: 101/Rl * C3H/HeA * C3H/Rl * C57BL/6JRn * C57/BLiA	N	MGI:2448159
MGI:2670731	F	MP:0000564	syndactyly	tmgc17/tmgc17	involves: 101/Rl * C3H/HeA * C3H/Rl * C57BL/6JRn * C57/BLiA	N	MGI:2448159
MGI:2670742	F	MP:0000592	short tail	Tmgc16/Tmgc16	involves: 101/Rl * C3H/HeA * C3H/Rl * C57BL/6JRn * C57/BLiA	N	MGI:2448159
MGI:2670742	F	MP:0000585	kinked tail	Tmgc16/Tmgc16	involves: 101/Rl * C3H/HeA * C3H/Rl * C57BL/6JRn * C57/BLiA	N	MGI:2448159
MGI:2670744	F	MP:0000585	kinked tail	Tmgc16/Tmgc16<+>	involves: 101/Rl * C3H/HeA * C3H/Rl * C57BL/6JRn * C57/BLiA	N	MGI:2448159
MGI:2670744	F	MP:0000592	short tail	Tmgc16/Tmgc16<+>	involves: 101/Rl * C3H/HeA * C3H/Rl * C57BL/6JRn * C57/BLiA	N	MGI:2448159
MGI:2670915	F	MP:0010252	anterior subcapsular cataract	Rgn<tm1Aish>/Rgn<tm1Aish>	involves: 129P2/OlaHsd * C57BL/6	N	22155581
MGI:2670915	F	MP:0011229	abnormal vitamin C level	Rgn<tm1Aish>/Rgn<tm1Aish>	involves: 129P2/OlaHsd * C57BL/6	N	22155581
MGI:2670915	F	MP:0003887	increased hepatocyte apoptosis	Rgn<tm1Aish>/Rgn<tm1Aish>	involves: 129P2/OlaHsd * C57BL/6	N	12368201
MGI:2670916	F	MP:0001868	ovary inflammation	Aod3<A/J>/?	A/J	N	12133995
MGI:2670916	F	MP:0004833	ovary atrophy	Aod3<A/J>/?	A/J	N	12133995
MGI:2670919	F	MP:0004833	ovary atrophy	Aod4<A/J>/?	A/J	N	12133995
MGI:2670955	F	MP:0031420	decreased superovulation rate	Ptx3<tm1Zuk>/Ptx3<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	12040004
MGI:2670955	F	MP:0009372	abnormal cumulus oophorus morphology	Ptx3<tm1Zuk>/Ptx3<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	12040004
MGI:2670955	F	MP:0009374	absent cumulus expansion	Ptx3<tm1Zuk>/Ptx3<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	12040004
MGI:2670955	F	MP:0001923	reduced female fertility	Ptx3<tm1Zuk>/Ptx3<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	12040004
MGI:2671055	F	MP:0002169	no abnormal phenotype detected	Igsf1<tm1Zuk>/Igsf1<tm1Zuk>	either: (involves: 129S6/SvEv * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	12832474
MGI:2671059	M	MP:0005119	decreased circulating thyroid-stimulating hormone level	Igsf1<tm1Zuk>/Y	either: (involves: 129S6/SvEv * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	23143598
MGI:2671059	M	MP:0000633	abnormal pituitary gland morphology	Igsf1<tm1Zuk>/Y	either: (involves: 129S6/SvEv * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	23143598
MGI:2671059	M	MP:0005479	decreased circulating triiodothyronine level	Igsf1<tm1Zuk>/Y	either: (involves: 129S6/SvEv * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	23143598
MGI:2671059	M	MP:0005389	reproductive system phenotype	Igsf1<tm1Zuk>/Y	either: (involves: 129S6/SvEv * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	Y	23143598
MGI:2671059	M	MP:0001260	increased body weight	Igsf1<tm1Zuk>/Y	either: (involves: 129S6/SvEv * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	23143598
MGI:2671059	M	MP:0005134	decreased thyroid-stimulating hormone level	Igsf1<tm1Zuk>/Y	either: (involves: 129S6/SvEv * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	23143598
MGI:2671059	M	MP:0003503	decreased activity of thyroid gland	Igsf1<tm1Zuk>/Y	either: (involves: 129S6/SvEv * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	23143598
MGI:2671059	M	MP:0005376	homeostasis/metabolism phenotype	Igsf1<tm1Zuk>/Y	either: (involves: 129S6/SvEv * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	Y	12832474
MGI:2671091	M	MP:0004852	decreased testis weight	Tkt<tm1Jpi>/Tkt<+>	involves: 129X1/SvJ * C57BL/6J	N	12167708
MGI:2671091	F	MP:0002566	abnormal sexual interaction	Tkt<tm1Jpi>/Tkt<+>	involves: 129X1/SvJ * C57BL/6J	N	12167708
MGI:2672021	M	MP:0001378	abnormal ejaculation	Etv4<tm1Hass>/Etv4<tm1Hass>	involves: 129S4/SvJae * BALB/c	N	11094084
MGI:2672021	F	MP:0000662	abnormal branching of the mammary ductal tree	Etv4<tm1Hass>/Etv4<tm1Hass>	involves: 129S4/SvJae * BALB/c	N	14635793
MGI:2672021	M	MP:0001925	male infertility	Etv4<tm1Hass>/Etv4<tm1Hass>	involves: 129S4/SvJae * BALB/c	N	11094084
MGI:2672136	M	MP:0001154	seminiferous tubule degeneration	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	N	11809801
MGI:2672136	M	MP:0001925	male infertility	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	N	11809801
MGI:2672136	M	MP:0002631	abnormal epididymis morphology	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	N	11809801
MGI:2672136	M	MP:0002687	oligozoospermia	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	N	11809801
MGI:2672136	M	MP:0001147	small testis	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	N	11809801
MGI:2672143	M	MP:0001925	male infertility	rmy/rmy	C3H/He-rmy	N	MGI:62480
MGI:2672838	F	MP:0001125	abnormal oocyte morphology	Cd9<tm1Mek>/Cd9<tm1Mek>	involves: 129/Sv * C57BL/6	N	22609062
MGI:2672838	F	MP:0001926	female infertility	Cd9<tm1Mek>/Cd9<tm1Mek>	involves: 129/Sv * C57BL/6	N	10634791
MGI:2673082	M	MP:0002216	abnormal seminiferous tubule morphology	Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	14994269
MGI:2673082	F	MP:0001923	reduced female fertility	Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	12748967
MGI:2673082	M	MP:0004852	decreased testis weight	Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	14994269
MGI:2673082	M	MP:0001156	abnormal spermatogenesis	Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	12748967
MGI:2673082	M	MP:0001156	abnormal spermatogenesis	Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	14994269
MGI:2673082	M	MP:0004901	decreased male germ cell number	Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	14994269
MGI:2673082	M	MP:0001147	small testis	Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	12748967
MGI:2673082	M	MP:0002687	oligozoospermia	Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	12748967
MGI:2673082	M	MP:0002687	oligozoospermia	Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	14994269
MGI:2673142	F	MP:0002637	small uterus	Trim25<tm1Mura>/Trim25<tm1Mura>	involves: 129/Sv * 129S4/SvJae	N	10518570
MGI:2673248	M	MP:0006380	abnormal spermatid morphology	Npepps<goku>/Npepps<goku>	involves: 129P2/OlaHsd * BALB/cA	N	11376114
MGI:2673248	M	MP:0001380	reduced male mating frequency	Npepps<goku>/Npepps<goku>	involves: 129P2/OlaHsd * BALB/cA	N	11376114
MGI:2673248	M	MP:0002687	oligozoospermia	Npepps<goku>/Npepps<goku>	involves: 129P2/OlaHsd * BALB/cA	N	11376114
MGI:2673248	M	MP:0002675	asthenozoospermia	Npepps<goku>/Npepps<goku>	involves: 129P2/OlaHsd * BALB/cA	N	11376114
MGI:2673248	M	MP:0002784	abnormal Sertoli cell morphology	Npepps<goku>/Npepps<goku>	involves: 129P2/OlaHsd * BALB/cA	N	11376114
MGI:2673248	M	MP:0001925	male infertility	Npepps<goku>/Npepps<goku>	involves: 129P2/OlaHsd * BALB/cA	N	11376114
MGI:2673248	M	MP:0001156	abnormal spermatogenesis	Npepps<goku>/Npepps<goku>	involves: 129P2/OlaHsd * BALB/cA	N	11376114
MGI:2673248	M	MP:0002216	abnormal seminiferous tubule morphology	Npepps<goku>/Npepps<goku>	involves: 129P2/OlaHsd * BALB/cA	N	11376114
MGI:2673248	M	MP:0001147	small testis	Npepps<goku>/Npepps<goku>	involves: 129P2/OlaHsd * BALB/cA	N	11376114
MGI:2673335	M	MP:0002216	abnormal seminiferous tubule morphology	Hmga1<tm1Cha>/Hmga1<+>	chimera involves: 129S1/Sv * C57BL/6J	N	12874803
MGI:2673335	M	MP:0001925	male infertility	Hmga1<tm1Cha>/Hmga1<+>	chimera involves: 129S1/Sv * C57BL/6J	N	12874803
MGI:2673335	M	MP:0001147	small testis	Hmga1<tm1Cha>/Hmga1<+>	chimera involves: 129S1/Sv * C57BL/6J	N	12874803
MGI:2673335	M	MP:0001156	abnormal spermatogenesis	Hmga1<tm1Cha>/Hmga1<+>	chimera involves: 129S1/Sv * C57BL/6J	N	12874803
MGI:2673335	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Hmga1<tm1Cha>/Hmga1<+>	chimera involves: 129S1/Sv * C57BL/6J	N	12874803
MGI:2673335	M	MP:0004901	decreased male germ cell number	Hmga1<tm1Cha>/Hmga1<+>	chimera involves: 129S1/Sv * C57BL/6J	N	12874803
MGI:2673335	M	MP:0004930	small epididymis	Hmga1<tm1Cha>/Hmga1<+>	chimera involves: 129S1/Sv * C57BL/6J	N	12874803
MGI:2673335	M	MP:0005159	azoospermia	Hmga1<tm1Cha>/Hmga1<+>	chimera involves: 129S1/Sv * C57BL/6J	N	12874803
MGI:2673335	M	MP:0002784	abnormal Sertoli cell morphology	Hmga1<tm1Cha>/Hmga1<+>	chimera involves: 129S1/Sv * C57BL/6J	N	12874803
MGI:2673335	M	MP:0001153	small seminiferous tubules	Hmga1<tm1Cha>/Hmga1<+>	chimera involves: 129S1/Sv * C57BL/6J	N	12874803
MGI:2673460	M	MP:0002216	abnormal seminiferous tubule morphology	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	N	12893777
MGI:2673460	M	MP:0002687	oligozoospermia	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	N	12893777
MGI:2673460	M	MP:0001147	small testis	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	N	12893777
MGI:2673460	M	MP:0006379	abnormal spermatocyte morphology	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	N	12893777
MGI:2673460	M	MP:0005169	abnormal male meiosis	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	N	12893777
MGI:2673460	F	MP:0008871	abnormal ovarian follicle number	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	N	12893777
MGI:2673543	M	MP:0001147	small testis	Rad23b<tm1Gvh>/Rad23b<tm1Gvh>	involves: 129P2/OlaHsd * C57BL/6	N	11809813
MGI:2673543	M	MP:0001155	arrest of spermatogenesis	Rad23b<tm1Gvh>/Rad23b<tm1Gvh>	involves: 129P2/OlaHsd * C57BL/6	N	11809813
MGI:2673543	F	MP:0001923	reduced female fertility	Rad23b<tm1Gvh>/Rad23b<tm1Gvh>	involves: 129P2/OlaHsd * C57BL/6	N	11809813
MGI:2673543	M	MP:0001925	male infertility	Rad23b<tm1Gvh>/Rad23b<tm1Gvh>	involves: 129P2/OlaHsd * C57BL/6	N	11809813
MGI:2673543	M	MP:0002784	abnormal Sertoli cell morphology	Rad23b<tm1Gvh>/Rad23b<tm1Gvh>	involves: 129P2/OlaHsd * C57BL/6	N	11809813
MGI:2673543	M	MP:0001153	small seminiferous tubules	Rad23b<tm1Gvh>/Rad23b<tm1Gvh>	involves: 129P2/OlaHsd * C57BL/6	N	11809813
MGI:2673732	M	MP:0002687	oligozoospermia	Akt1<tm1Nhy>/Akt1<tm1Nhy>	involves: 129/Sv * C57BL/6	N	11544177
MGI:2673732	M	MP:0001153	small seminiferous tubules	Akt1<tm1Nhy>/Akt1<tm1Nhy>	involves: 129/Sv * C57BL/6	N	11544177
MGI:2673732	M	MP:0001156	abnormal spermatogenesis	Akt1<tm1Nhy>/Akt1<tm1Nhy>	involves: 129/Sv * C57BL/6	N	11544177
MGI:2673732	M	MP:0020550	multinucleated giant male germ cells	Akt1<tm1Nhy>/Akt1<tm1Nhy>	involves: 129/Sv * C57BL/6	N	11544177
MGI:2673732	M	MP:0001154	seminiferous tubule degeneration	Akt1<tm1Nhy>/Akt1<tm1Nhy>	involves: 129/Sv * C57BL/6	N	11544177
MGI:2673732	M	MP:0001146	abnormal testis morphology	Akt1<tm1Nhy>/Akt1<tm1Nhy>	involves: 129/Sv * C57BL/6	N	11544177
MGI:2674001	F	MP:0009010	abnormal diestrus	Nr6a1<tm3Coo>/Nr6a1<tm3Coo>,Tg(Zp3-cre)93Knw/0	involves: 129S7/SvEvBrd * C57BL/6	N	12912906
MGI:2674001	F	MP:0001125	abnormal oocyte morphology	Nr6a1<tm3Coo>/Nr6a1<tm3Coo>,Tg(Zp3-cre)93Knw/0	involves: 129S7/SvEvBrd * C57BL/6	N	12912906
MGI:2674001	F	MP:0009011	prolonged diestrus	Nr6a1<tm3Coo>/Nr6a1<tm3Coo>,Tg(Zp3-cre)93Knw/0	involves: 129S7/SvEvBrd * C57BL/6	N	12912906
MGI:2674001	F	MP:0009433	polyovular ovarian follicle	Nr6a1<tm3Coo>/Nr6a1<tm3Coo>,Tg(Zp3-cre)93Knw/0	involves: 129S7/SvEvBrd * C57BL/6	N	12912906
MGI:2674001	F	MP:0009006	prolonged estrous cycle	Nr6a1<tm3Coo>/Nr6a1<tm3Coo>,Tg(Zp3-cre)93Knw/0	involves: 129S7/SvEvBrd * C57BL/6	N	12912906
MGI:2674001	F	MP:0001923	reduced female fertility	Nr6a1<tm3Coo>/Nr6a1<tm3Coo>,Tg(Zp3-cre)93Knw/0	involves: 129S7/SvEvBrd * C57BL/6	N	12912906
MGI:2674073	M	MP:0001262	decreased body weight	Hint1<tm1Ibw>/Hint1<tm1Ibw>	involves: 129 * C57BL/6	N	12810953
MGI:2674195	M	MP:0002769	abnormal vas deferens morphology	Brd4<Gt(pGT1.8TM)ST132Nimr>/Brd4<+>	involves: 129P2/Ola * C57BL/6J	N	11997514
MGI:2674195	M	MP:0001156	abnormal spermatogenesis	Brd4<Gt(pGT1.8TM)ST132Nimr>/Brd4<+>	involves: 129P2/Ola * C57BL/6J	N	11997514
MGI:2674195	M	MP:0004933	abnormal epididymis epithelium morphology	Brd4<Gt(pGT1.8TM)ST132Nimr>/Brd4<+>	involves: 129P2/Ola * C57BL/6J	N	11997514
MGI:2674195	M	MP:0002216	abnormal seminiferous tubule morphology	Brd4<Gt(pGT1.8TM)ST132Nimr>/Brd4<+>	involves: 129P2/Ola * C57BL/6J	N	11997514
MGI:2674270	M	MP:0001153	small seminiferous tubules	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0001925	male infertility	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0002780	decreased circulating testosterone level	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0005536	decreased Leydig cell number	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0004884	abnormal testis physiology	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0014269	decreased testes secretion	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0005578	teratozoospermia	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0002687	oligozoospermia	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0004901	decreased male germ cell number	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0020362	abnormal male germ cell physiology	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0004852	decreased testis weight	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0003674	oxidative stress	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0009230	abnormal sperm head morphology	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0005319	abnormal enzyme/coenzyme level	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0001147	small testis	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0009231	detached acrosome	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0002631	abnormal epididymis morphology	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0009233	enlarged sperm head	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0009232	abnormal sperm nucleus morphology	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674270	M	MP:0014052	increased male germ cell apoptosis	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd	N	29559852
MGI:2674946	M	MP:0002207	abnormal long-term potentiation	Gria3<tm1Zpj>/Y	involves: 129/Sv * C57BL/6	N	12848940
MGI:2674946	M	MP:0001922	reduced male fertility	Gria3<tm1Zpj>/Y	involves: 129/Sv * C57BL/6	N	12848940
MGI:2674946	M	MP:0002161	abnormal fertility/fecundity	Gria3<tm1Zpj>/Y	involves: 129/Sv * C57BL/6	N	12848940
MGI:2674947	M	MP:0003631	nervous system phenotype	Gria2<tm1Rod>/Gria2<tm1Rod>,Gria3<tm1Zpj>/Y	involves: 129/Sv * C57BL/6	Y	12848940
MGI:2674947	M	MP:0004859	abnormal synaptic plasticity	Gria2<tm1Rod>/Gria2<tm1Rod>,Gria3<tm1Zpj>/Y	involves: 129/Sv * C57BL/6	N	12848940
MGI:2674947	M	MP:0001402	decreased locomotor activity	Gria2<tm1Rod>/Gria2<tm1Rod>,Gria3<tm1Zpj>/Y	involves: 129/Sv * C57BL/6	N	12848940
MGI:2674947	M	MP:0002912	abnormal excitatory postsynaptic potential	Gria2<tm1Rod>/Gria2<tm1Rod>,Gria3<tm1Zpj>/Y	involves: 129/Sv * C57BL/6	N	12848940
MGI:2674947	M	MP:0001265	decreased body size	Gria2<tm1Rod>/Gria2<tm1Rod>,Gria3<tm1Zpj>/Y	involves: 129/Sv * C57BL/6	N	12848940
MGI:2674947	M	MP:0001898	abnormal long-term depression	Gria2<tm1Rod>/Gria2<tm1Rod>,Gria3<tm1Zpj>/Y	involves: 129/Sv * C57BL/6	N	12848940
MGI:2674947	M	MP:0002066	abnormal motor capabilities/coordination/movement	Gria2<tm1Rod>/Gria2<tm1Rod>,Gria3<tm1Zpj>/Y	involves: 129/Sv * C57BL/6	N	12848940
MGI:2674947	M	MP:0003008	enhanced long-term potentiation	Gria2<tm1Rod>/Gria2<tm1Rod>,Gria3<tm1Zpj>/Y	involves: 129/Sv * C57BL/6	N	12848940
MGI:2674947	M	MP:0000745	tremors	Gria2<tm1Rod>/Gria2<tm1Rod>,Gria3<tm1Zpj>/Y	involves: 129/Sv * C57BL/6	N	12848940
MGI:2674947	M	MP:0011086	postnatal lethality, incomplete penetrance	Gria2<tm1Rod>/Gria2<tm1Rod>,Gria3<tm1Zpj>/Y	involves: 129/Sv * C57BL/6	N	12848940
MGI:2674948	F	MP:0009504	abnormal mammary gland epithelium morphology	Pgr<tm2Omc>/Pgr<tm2Omc>	involves: 129S7/SvEvBrd * C57BL/6	N	12897242
MGI:2674948	F	MP:0000662	abnormal branching of the mammary ductal tree	Pgr<tm2Omc>/Pgr<tm2Omc>	involves: 129S7/SvEvBrd * C57BL/6	N	12897242
MGI:2674948	F	MP:0006269	abnormal mammary gland growth during pregnancy	Pgr<tm2Omc>/Pgr<tm2Omc>	involves: 129S7/SvEvBrd * C57BL/6	N	12897242
MGI:2674948	F	MP:0009506	abnormal mammary gland alveolus morphology	Pgr<tm2Omc>/Pgr<tm2Omc>	involves: 129S7/SvEvBrd * C57BL/6	N	12897242
MGI:2674948	F	MP:0001882	abnormal lactation	Pgr<tm2Omc>/Pgr<tm2Omc>	involves: 129S7/SvEvBrd * C57BL/6	N	12897242
MGI:2674973	M	MP:0001147	small testis	Spmap2<tm1Wen>/Spmap2<tm1Wen>	involves: 129S1/Sv * 129X1/SvJ	N	12748127
MGI:2674974	M	MP:0001147	small testis	Spmap2<tm1Wen>/Spmap2<tm1Wen>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12748127
MGI:2675034	F	MP:0005027	increased susceptibility to parasitic infection	Lmr1<BALB/c>/Lmr1<BALB/c>,Lmr30<C57BL/6>/Lmr30<C57BL/6>	involves: BALB/c * C57BL/6	N	10508279
MGI:2675035	F	MP:0005027	increased susceptibility to parasitic infection	Lmr1<BALB/c>/Lmr1<BALB/c>,Lmr30<C57BL/6>/Lmr30<BALB/c>	involves: BALB/c * C57BL/6	N	10508279
MGI:2675155	F	MP:0000745	tremors	Gjc2<tm1Paul>/Gjc2<tm1Paul>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129/Sv * C57BL/6	N	12843301
MGI:2675155	F	MP:0001333	absent optic nerve	Gjc2<tm1Paul>/Gjc2<tm1Paul>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129/Sv * C57BL/6	N	12843301
MGI:2675155	F	MP:0002826	tonic seizures	Gjc2<tm1Paul>/Gjc2<tm1Paul>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129/Sv * C57BL/6	N	12843301
MGI:2675155	F	MP:0000921	demyelination	Gjc2<tm1Paul>/Gjc2<tm1Paul>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129/Sv * C57BL/6	N	12843301
MGI:2675155	F	MP:0002083	premature death	Gjc2<tm1Paul>/Gjc2<tm1Paul>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129/Sv * C57BL/6	N	12843301
MGI:2675155	F	MP:0000920	abnormal myelination	Gjc2<tm1Paul>/Gjc2<tm1Paul>,Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129/Sv * C57BL/6	N	12843301
MGI:2675234	F	MP:0004256	abnormal maternal decidual layer morphology	Akt1<tm1Hem>/Akt1<tm1Hem>	involves: 129P2/OlaHsd * C57BL/6	N	12783884
MGI:2675289	F	MP:0001923	reduced female fertility	Ptx3<tm1Mant>/Ptx3<tm1Mant>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	12432394
MGI:2675290	F	MP:0001120	abnormal uterus morphology	Col1a1<tm1Jae>/Col1a1<tm1Jae>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	N	7790374
MGI:2675290	F	MP:0008256	abnormal myometrium morphology	Col1a1<tm1Jae>/Col1a1<tm1Jae>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	N	7790374
MGI:2675291	F	MP:0001120	abnormal uterus morphology	Col1a1<tm1Jae>/Col1a1<+>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	N	7790374
MGI:2675314	F	MP:0001923	reduced female fertility	Tcl1<tm1Rso>/Tcl1<tm1Rso>	involves: 129X1/SvJ * C57BL/6	N	12181493
MGI:2675315	F	MP:0001923	reduced female fertility	kkt/kkt	involves: C57BL/6 * CBA	N	10656775
MGI:2675319	F	MP:0001926	female infertility	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	N	11889050
MGI:2675319	F	MP:0004805	absent oocytes	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	N	11889050
MGI:2675319	F	MP:0002777	absent ovarian follicles	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	N	11889050
MGI:2675319	F	MP:0013236	ovary degeneration	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	N	11889050
MGI:2675470	M	MP:0002717	abnormal male preputial gland morphology	Traf6<tm1Jino>/Traf6<tm1Jino>	involves: 129P2/OlaHsd * C57BL/6	N	12060722
MGI:2675491	M	MP:0001940	testis hypoplasia	Ccne1<tm1Pisc>/Ccne1<+>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	N	12941272
MGI:2675491	M	MP:0001922	reduced male fertility	Ccne1<tm1Pisc>/Ccne1<+>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	N	12941272
MGI:2675496	M	MP:0001925	male infertility	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	N	12941272
MGI:2675496	M	MP:0005169	abnormal male meiosis	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	N	12941272
MGI:2675496	M	MP:0020550	multinucleated giant male germ cells	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	N	12941272
MGI:2675496	M	MP:0001147	small testis	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	N	12941272
MGI:2675496	M	MP:0002216	abnormal seminiferous tubule morphology	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	N	12941272
MGI:2675496	M	MP:0003205	testicular atrophy	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	N	12941272
MGI:2675496	M	MP:0002687	oligozoospermia	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	N	12941272
MGI:2675496	M	MP:0001156	abnormal spermatogenesis	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	N	12941272
MGI:2675622	F	MP:0004833	ovary atrophy	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	N	12923533
MGI:2675622	F	MP:0001119	abnormal female reproductive system morphology	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	N	12923533
MGI:2675622	M	MP:0002216	abnormal seminiferous tubule morphology	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	N	12923533
MGI:2675622	F	MP:0001125	abnormal oocyte morphology	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	N	12923533
MGI:2675622	M	MP:0001145	abnormal male reproductive system morphology	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	N	12923533
MGI:2675622	F	MP:0002777	absent ovarian follicles	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	N	12923533
MGI:2675622	M	MP:0001932	abnormal spermiogenesis	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	N	12923533
MGI:2675622	M	MP:0003205	testicular atrophy	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	N	12923533
MGI:2675622	F	MP:0001134	absent corpus luteum	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	N	12923533
MGI:2675764	F	MP:0013348	adenohypophysis hyperplasia	Drd2<tm1Ebo>/Drd2<tm1Ebo>	involves: 129S2/SvPas * C57BL/6	N	9247268
MGI:2675764	F	MP:0001923	reduced female fertility	Drd2<tm1Ebo>/Drd2<tm1Ebo>	involves: 129S2/SvPas * C57BL/6	N	9247268
MGI:2675764	F	MP:0008371	pituitary intermediate lobe hyperplasia	Drd2<tm1Ebo>/Drd2<tm1Ebo>	involves: 129S2/SvPas * C57BL/6	N	9247268
MGI:2675764	M	MP:0001147	small testis	Drd2<tm1Ebo>/Drd2<tm1Ebo>	involves: 129S2/SvPas * C57BL/6	N	7566118
MGI:2675764	F	MP:0001127	small ovary	Drd2<tm1Ebo>/Drd2<tm1Ebo>	involves: 129S2/SvPas * C57BL/6	N	7566118
MGI:2675764	F	MP:0009016	abnormal estrus	Drd2<tm1Ebo>/Drd2<tm1Ebo>	involves: 129S2/SvPas * C57BL/6	N	9247268
MGI:2675764	F	MP:0009011	prolonged diestrus	Drd2<tm1Ebo>/Drd2<tm1Ebo>	involves: 129S2/SvPas * C57BL/6	N	9247268
MGI:2675764	F	MP:0001927	abnormal estrous cycle	Drd2<tm1Ebo>/Drd2<tm1Ebo>	involves: 129S2/SvPas * C57BL/6	N	9247268
MGI:2675990	M	MP:0001922	reduced male fertility	Mfge8<tm1Shur>/Mfge8<tm1Shur>	involves: 129 * C57BL/6	N	12941270
MGI:2675990	M	MP:0030978	impaired binding of sperm to zona pellucida	Mfge8<tm1Shur>/Mfge8<tm1Shur>	involves: 129 * C57BL/6	N	12941270
MGI:2675997	M	MP:0020550	multinucleated giant male germ cells	Bad<tm1Sjk>/Bad<tm1Sjk>	either: 129X1/SvJ or (involves: 129X1/SvJ * C57BL/6)	N	12876200
MGI:2675997	M	MP:0001146	abnormal testis morphology	Bad<tm1Sjk>/Bad<tm1Sjk>	either: 129X1/SvJ or (involves: 129X1/SvJ * C57BL/6)	N	12876200
MGI:2676099	M	MP:0010275	increased melanoma incidence	Cdkn2a<tm1Nesh>/Cdkn2a<tm1Nesh>,X/Tg(Tyr-HRAS)60Lc	involves: 129S6/SvEvTac * C57BL/6J * CBA/J * FVB	N	12902988
MGI:2676124	M	MP:0010275	increased melanoma incidence	Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>,X/Tg(Tyr-HRAS)60Lc	involves: 129S6/SvEvTac * C57BL/6J * CBA/J * FVB	N	12902988
MGI:2676253	M	MP:0008584	photoreceptor outer segment degeneration	Ndp<tm1Wbrg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8789439
MGI:2676253	M	MP:0001328	disorganized retina layers	Ndp<tm1Wbrg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8789439
MGI:2676253	M	MP:0005103	abnormal retina pigmentation	Ndp<tm1Wbrg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8789439
MGI:2676253	M	MP:0001327	decreased retina photoreceptor cell number	Ndp<tm1Wbrg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8789439
MGI:2676253	M	MP:0003731	abnormal retina outer nuclear layer morphology	Ndp<tm1Wbrg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8789439
MGI:2676253	M	MP:0003728	abnormal retina photoreceptor layer morphology	Ndp<tm1Wbrg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8789439
MGI:2676253	M	MP:0008509	disorganized retina ganglion layer	Ndp<tm1Wbrg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8789439
MGI:2676253	M	MP:0003733	abnormal retina inner nuclear layer morphology	Ndp<tm1Wbrg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8789439
MGI:2676253	M	MP:0006200	vitreous body deposition	Ndp<tm1Wbrg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8789439
MGI:2676253	M	MP:0003732	abnormal retina outer plexiform layer morphology	Ndp<tm1Wbrg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8789439
MGI:2676253	M	MP:0002699	abnormal vitreous body morphology	Ndp<tm1Wbrg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	8789439
MGI:2676263	F	MP:0005391	vision/eye phenotype	Ndp<tm1Wbrg>/Ndp<+>	involves: 129P2/OlaHsd * C57BL/6	Y	8789439
MGI:2676345	F	MP:0003355	decreased ovulation rate	Mfsd12<gr>/Mfsd12<gr>	involves: A * STOCK fz	N	MGI:60250
MGI:2676345	F	MP:0001928	abnormal ovulation	Mfsd12<gr>/Mfsd12<gr>	involves: A * STOCK fz	N	MGI:60250
MGI:2676425	F	MP:0001923	reduced female fertility	Wnt3a<vt>/Wnt3a<vt>	involves: C57BR	N	14832454
MGI:2677141	F	MP:0009666	abnormal embryo attachment	Lif<tm1Phb>/Lif<tm1Phb>	involves: 129S2/SvPas * C57BL/6 * DBA/2	N	10935540
MGI:2677141	F	MP:0001728	failure of embryo implantation	Lif<tm1Phb>/Lif<tm1Phb>	involves: 129S2/SvPas * C57BL/6 * DBA/2	N	10935540
MGI:2677141	F	MP:0009665	abnormal embryo apposition	Lif<tm1Phb>/Lif<tm1Phb>	involves: 129S2/SvPas * C57BL/6 * DBA/2	N	10935540
MGI:2677141	F	MP:0001926	female infertility	Lif<tm1Phb>/Lif<tm1Phb>	involves: 129S2/SvPas * C57BL/6 * DBA/2	N	10935540
MGI:2677141	F	MP:0009662	abnormal uterine receptivity	Lif<tm1Phb>/Lif<tm1Phb>	involves: 129S2/SvPas * C57BL/6 * DBA/2	N	10935540
MGI:2677141	F	MP:0001926	female infertility	Lif<tm1Phb>/Lif<tm1Phb>	involves: 129S2/SvPas * C57BL/6 * DBA/2	N	8497320
MGI:2677273	F	MP:0001384	abnormal pup retrieval	Mest<tm1Masu>/Mest<+>	involves: 129S1/Sv * 129X1/SvJ	N	9771709
MGI:2677273	F	MP:0001386	abnormal maternal nurturing	Mest<tm1Masu>/Mest<+>	involves: 129S1/Sv * 129X1/SvJ	N	9771709
MGI:2677317	M	MP:0003642	absent seminal vesicle	Pax2<tm1Pgr>/Pax2<tm1Pgr>	involves: 129S1/Sv * 129X1/SvJ	N	8575306
MGI:2677317	F	MP:0009215	absent uterine horn	Pax2<tm1Pgr>/Pax2<tm1Pgr>	involves: 129S1/Sv * 129X1/SvJ	N	8575306
MGI:2677317	F	MP:0003575	absent oviduct	Pax2<tm1Pgr>/Pax2<tm1Pgr>	involves: 129S1/Sv * 129X1/SvJ	N	8575306
MGI:2677317	F	MP:0003535	absent vagina	Pax2<tm1Pgr>/Pax2<tm1Pgr>	involves: 129S1/Sv * 129X1/SvJ	N	8575306
MGI:2677317	M	MP:0003557	absent vas deferens	Pax2<tm1Pgr>/Pax2<tm1Pgr>	involves: 129S1/Sv * 129X1/SvJ	N	8575306
MGI:2677317	M	MP:0004729	absent efferent ductules of testis	Pax2<tm1Pgr>/Pax2<tm1Pgr>	involves: 129S1/Sv * 129X1/SvJ	N	8575306
MGI:2677317	M	MP:0004727	absent epididymis	Pax2<tm1Pgr>/Pax2<tm1Pgr>	involves: 129S1/Sv * 129X1/SvJ	N	8575306
MGI:2677317	M	MP:0001146	abnormal testis morphology	Pax2<tm1Pgr>/Pax2<tm1Pgr>	involves: 129S1/Sv * 129X1/SvJ	N	8575306
MGI:2677347	F	MP:0002169	no abnormal phenotype detected	Gata1<tm1Phi>/Gata1<tm1Phi>	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	12954777
MGI:2677348	M	MP:0002169	no abnormal phenotype detected	Gata1<tm1Phi>/Y	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	12954777
MGI:2677349	M	MP:0002169	no abnormal phenotype detected	Gata1<tm1Phi>/Y,Tg(Dhh-cre)1Mejr/0	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	12954777
MGI:2677376	M	MP:0002687	oligozoospermia	Sirt1<tm1Fwa>/Sirt1<tm1Fwa>	involves: 129/Sv * 129S6/SvEvTac	N	12960381
MGI:2677468	M	MP:0001925	male infertility	Lipe<tm1Land>/Lipe<tm1Land>	involves: 129 * C57BL/6J	N	12835327
MGI:2677468	M	MP:0002687	oligozoospermia	Lipe<tm1Land>/Lipe<tm1Land>	involves: 129 * C57BL/6J	N	12835327
MGI:2677502	M	MP:0001156	abnormal spermatogenesis	Tsn<Gt(OST63223)Lex>/Tsn<Gt(OST63223)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	12944470
MGI:2677502	M	MP:0002687	oligozoospermia	Tsn<Gt(OST63223)Lex>/Tsn<Gt(OST63223)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	12944470
MGI:2677502	M	MP:0014052	increased male germ cell apoptosis	Tsn<Gt(OST63223)Lex>/Tsn<Gt(OST63223)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	12944470
MGI:2677502	F	MP:0001923	reduced female fertility	Tsn<Gt(OST63223)Lex>/Tsn<Gt(OST63223)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	12944470
MGI:2677502	M	MP:0008261	arrest of male meiosis	Tsn<Gt(OST63223)Lex>/Tsn<Gt(OST63223)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	12944470
MGI:2677502	M	MP:0001154	seminiferous tubule degeneration	Tsn<Gt(OST63223)Lex>/Tsn<Gt(OST63223)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	12944470
MGI:2677502	M	MP:0001146	abnormal testis morphology	Tsn<Gt(OST63223)Lex>/Tsn<Gt(OST63223)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	12944470
MGI:2677715	M	MP:0002687	oligozoospermia	Ccne2<tm1Boa>/Ccne2<tm1Boa>	involves: 129/Sv * C57BL/6	N	12970191
MGI:2677715	M	MP:0001922	reduced male fertility	Ccne2<tm1Boa>/Ccne2<tm1Boa>	involves: 129/Sv * C57BL/6	N	12970191
MGI:2677715	M	MP:0001147	small testis	Ccne2<tm1Boa>/Ccne2<tm1Boa>	involves: 129/Sv * C57BL/6	N	12970191
MGI:2677718	F	MP:0001882	abnormal lactation	Ghrhr<lit>/Ghrhr<lit>	C57BL/6J-Ghrhr<lit>	N	1270792
MGI:2677718	M	MP:0001922	reduced male fertility	Ghrhr<lit>/Ghrhr<lit>	C57BL/6J-Ghrhr<lit>	N	1270792
MGI:2677759	M	MP:0005250	decreased Sertoli cell number	Vhl<tm1Lss>/Vhl<tm1.1Lss>,Tg(ACTB-cre)1Tes/0	involves: 129X1/SvJ * C3H * C57BL/6	N	14500363
MGI:2677759	M	MP:0001154	seminiferous tubule degeneration	Vhl<tm1Lss>/Vhl<tm1.1Lss>,Tg(ACTB-cre)1Tes/0	involves: 129X1/SvJ * C3H * C57BL/6	N	14500363
MGI:2677759	M	MP:0001925	male infertility	Vhl<tm1Lss>/Vhl<tm1.1Lss>,Tg(ACTB-cre)1Tes/0	involves: 129X1/SvJ * C3H * C57BL/6	N	14500363
MGI:2677759	M	MP:0002687	oligozoospermia	Vhl<tm1Lss>/Vhl<tm1.1Lss>,Tg(ACTB-cre)1Tes/0	involves: 129X1/SvJ * C3H * C57BL/6	N	14500363
MGI:2677759	M	MP:0020550	multinucleated giant male germ cells	Vhl<tm1Lss>/Vhl<tm1.1Lss>,Tg(ACTB-cre)1Tes/0	involves: 129X1/SvJ * C3H * C57BL/6	N	14500363
MGI:2677759	M	MP:0001147	small testis	Vhl<tm1Lss>/Vhl<tm1.1Lss>,Tg(ACTB-cre)1Tes/0	involves: 129X1/SvJ * C3H * C57BL/6	N	14500363
MGI:2677761	M	MP:0002687	oligozoospermia	Vhl<tm1Lss>/Vhl<tm1.1Lss>	involves: 129X1/SvJ * C57BL/6	N	14500363
MGI:2677778	M	MP:0001925	male infertility	Gusb<mps>/Gusb<mps>	involves: C57BL/6By	N	MGI:62101
MGI:2677778	F	MP:0001882	abnormal lactation	Gusb<mps>/Gusb<mps>	involves: C57BL/6By	N	MGI:62101
MGI:2677854	F	MP:0001385	pup cannibalization	Sftpb<tm1Jaw>/Sftpb<tm1Jaw>	involves: 129S2/SvPas * Black Swiss	N	7644495
MGI:2677888	M	MP:0009230	abnormal sperm head morphology	Nectin2<tm1Smu>/Nectin2<tm1Smu>	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	12801998
MGI:2677888	M	MP:0004542	impaired acrosome reaction	Nectin2<tm1Smu>/Nectin2<tm1Smu>	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	12801998
MGI:2677888	M	MP:0004543	abnormal sperm physiology	Nectin2<tm1Smu>/Nectin2<tm1Smu>	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	12801998
MGI:2677888	M	MP:0030978	impaired binding of sperm to zona pellucida	Nectin2<tm1Smu>/Nectin2<tm1Smu>	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	12801998
MGI:2677888	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Nectin2<tm1Smu>/Nectin2<tm1Smu>	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	12801998
MGI:2677888	M	MP:0005578	teratozoospermia	Nectin2<tm1Smu>/Nectin2<tm1Smu>	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	12801998
MGI:2677888	M	MP:0009831	abnormal sperm midpiece morphology	Nectin2<tm1Smu>/Nectin2<tm1Smu>	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	12801998
MGI:2677888	M	MP:0001925	male infertility	Nectin2<tm1Smu>/Nectin2<tm1Smu>	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	12801998
MGI:2677888	M	MP:0031012	impaired sperm migration in female genital tract	Nectin2<tm1Smu>/Nectin2<tm1Smu>	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	12801998
MGI:2677888	M	MP:0031389	abnormal ectoplasmic specialization morphology	Nectin2<tm1Smu>/Nectin2<tm1Smu>	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	12801998
MGI:2677907	M	MP:0001922	reduced male fertility	gri/gri	C3H/HeSnJ-gri/J	N	11130986
MGI:2677931	M	MP:0005159	azoospermia	gro25/gro25	Not Specified	N	12955145
MGI:2677932	M	MP:0005159	azoospermia	gro26/gro26	Not Specified	N	12955145
MGI:2678052	F	MP:0001262	decreased body weight	C10bw6<M. m. castaneus>/C10bw6<M. m. castaneus>	involves: C57BL/6J * M. m. castaneus	N	11003694
MGI:2678053	F	MP:0001262	decreased body weight	C10bw6<C57BL/6J>/C10bw6<M. m. castaneus>	involves: C57BL/6J * M. m. castaneus	N	11003694
MGI:2678469	M	MP:0008700	decreased interleukin-4 secretion	Hprt1<b-m3>/Y,Impdh1<tm1Bmi>/Impdh1<tm1Bmi>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	12944494
MGI:2678469	M	MP:0005079	decreased cytotoxic T cell cytolysis	Hprt1<b-m3>/Y,Impdh1<tm1Bmi>/Impdh1<tm1Bmi>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	12944494
MGI:2678469	M	MP:0005095	decreased T cell proliferation	Hprt1<b-m3>/Y,Impdh1<tm1Bmi>/Impdh1<tm1Bmi>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	12944494
MGI:2678469	M	MP:0002401	abnormal lymphopoiesis	Hprt1<b-m3>/Y,Impdh1<tm1Bmi>/Impdh1<tm1Bmi>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	12944494
MGI:2678469	M	MP:0009335	decreased splenocyte proliferation	Hprt1<b-m3>/Y,Impdh1<tm1Bmi>/Impdh1<tm1Bmi>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	12944494
MGI:2678480	M	MP:0005078	abnormal cytotoxic T cell physiology	Hprt1<b-m3>/Y,Impdh2<tm1Bmi>/Impdh2<+>	involves: 129P2/OlaHsd	N	10953035
MGI:2678480	M	MP:0000717	abnormal lymphocyte cell number	Hprt1<b-m3>/Y,Impdh2<tm1Bmi>/Impdh2<+>	involves: 129P2/OlaHsd	N	10953035
MGI:2678495	M	MP:0002687	oligozoospermia	Pias2<Gt(pT1Betageo)1Ruiz>/Pias2<Gt(pT1Betageo)1Ruiz>	involves: 129P2/OlaHsd * C57BL/6	N	15956336
MGI:2678495	M	MP:0001146	abnormal testis morphology	Pias2<Gt(pT1Betageo)1Ruiz>/Pias2<Gt(pT1Betageo)1Ruiz>	involves: 129P2/OlaHsd * C57BL/6	N	15956336
MGI:2678495	M	MP:0005389	reproductive system phenotype	Pias2<Gt(pT1Betageo)1Ruiz>/Pias2<Gt(pT1Betageo)1Ruiz>	involves: 129P2/OlaHsd * C57BL/6	Y	15956336
MGI:2678495	M	MP:0006042	increased apoptosis	Pias2<Gt(pT1Betageo)1Ruiz>/Pias2<Gt(pT1Betageo)1Ruiz>	involves: 129P2/OlaHsd * C57BL/6	N	15956336
MGI:2678495	M	MP:0004884	abnormal testis physiology	Pias2<Gt(pT1Betageo)1Ruiz>/Pias2<Gt(pT1Betageo)1Ruiz>	involves: 129P2/OlaHsd * C57BL/6	N	15956336
MGI:2678495	M	MP:0001153	small seminiferous tubules	Pias2<Gt(pT1Betageo)1Ruiz>/Pias2<Gt(pT1Betageo)1Ruiz>	involves: 129P2/OlaHsd * C57BL/6	N	15956336
MGI:2678495	M	MP:0002160	abnormal reproductive system morphology	Pias2<Gt(pT1Betageo)1Ruiz>/Pias2<Gt(pT1Betageo)1Ruiz>	involves: 129P2/OlaHsd * C57BL/6	N	15956336
MGI:2678495	M	MP:0005378	growth/size/body region phenotype	Pias2<Gt(pT1Betageo)1Ruiz>/Pias2<Gt(pT1Betageo)1Ruiz>	involves: 129P2/OlaHsd * C57BL/6	Y	15956336
MGI:2678495	M	MP:0004852	decreased testis weight	Pias2<Gt(pT1Betageo)1Ruiz>/Pias2<Gt(pT1Betageo)1Ruiz>	involves: 129P2/OlaHsd * C57BL/6	N	15956336
MGI:2678497	F	MP:0002169	no abnormal phenotype detected	Dmd<Gt(pT1ATGBetageo)1Ruiz>/Dmd<Gt(pT1ATGBetageo)1Ruiz>	involves: 129S2/SvPas * C57BL/6	N	12904583
MGI:2678575	F	MP:0000008	increased white adipose tissue amount	Fob4<F line>/Fob4<F line>	involves: F line * L line	N	10602985
MGI:2678576	F	MP:0000008	increased white adipose tissue amount	Fob4<F line>/Fob4<L line>	involves: F line * L line	N	10602985
MGI:2678771	F	MP:0002090	abnormal vision	Opn1mw<tm1(OPN1LW)Nat>/Opn1mw<+>	involves: 129	N	14500905
MGI:2678773	F	MP:0002090	abnormal vision	Opn1mw<tm1(OPN1LW)Nat>/Opn1mw<tm1(OPN1LW)Nat>	involves: 129	N	14500905
MGI:2678774	M	MP:0002090	abnormal vision	Opn1mw<tm1(OPN1LW)Nat>/Y	involves: 129	N	14500905
MGI:2679026	M	MP:0005018	decreased T cell number	Ikbkg<tm1.1Mpa>/Y,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	14499113
MGI:2679026	M	MP:0008083	decreased single-positive T cell number	Ikbkg<tm1.1Mpa>/Y,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	14499113
MGI:2679026	M	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Ikbkg<tm1.1Mpa>/Y,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	14499113
MGI:2679026	M	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Ikbkg<tm1.1Mpa>/Y,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	14499113
MGI:2679026	M	MP:0006413	increased T cell apoptosis	Ikbkg<tm1.1Mpa>/Y,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	14499113
MGI:2679598	F	MP:0010249	lactation failure	Tg(MMTV-PyVT)634Mul/0	FVB/N-Tg(MMTV-PyVT)634Mul/Nci	N	1312220
MGI:2679647	M	MP:0004542	impaired acrosome reaction	Cplx1<tm2Bros>/Cplx1<tm2Bros>	Not Specified	N	17692307
MGI:2679647	M	MP:0004542	impaired acrosome reaction	Cplx1<tm2Bros>/Cplx1<tm2Bros>	Not Specified	N	18577553
MGI:2679647	M	MP:0001265	decreased body size	Cplx1<tm2Bros>/Cplx1<tm2Bros>	Not Specified	N	18577553
MGI:2679647	M	MP:0005389	reproductive system phenotype	Cplx1<tm2Bros>/Cplx1<tm2Bros>	Not Specified	Y	18577553
MGI:2679647	M	MP:0001925	male infertility	Cplx1<tm2Bros>/Cplx1<tm2Bros>	Not Specified	N	18577553
MGI:2679647	M	MP:0002675	asthenozoospermia	Cplx1<tm2Bros>/Cplx1<tm2Bros>	Not Specified	N	18577553
MGI:2679647	M	MP:0002566	abnormal sexual interaction	Cplx1<tm2Bros>/Cplx1<tm2Bros>	Not Specified	N	18577553
MGI:2679680	M	MP:0002216	abnormal seminiferous tubule morphology	Slc19a1<tm1Gold>/Slc19a1<tm1Gold>	involves: 129/Sv * C57BL/6 * SJL	N	11266438
MGI:2679681	M	MP:0010968	decreased compact bone area	Bmd16<C3H/HeJ>/Bmd16<C3H/HeJ>	involves: C3H/HeJ * C57BL/6J	N	14667144
MGI:2679681	M	MP:0004991	decreased bone strength	Bmd16<C3H/HeJ>/Bmd16<C3H/HeJ>	involves: C3H/HeJ * C57BL/6J	N	14667144
MGI:2679687	M	MP:0010968	decreased compact bone area	Bmd5<C3H/HeJ>/Bmd5<C3H/HeJ>	involves: C3H/HeJ * C57BL/6J	N	14667144
MGI:2679695	F	MP:0013616	decreased volumetric bone mineral density	Bmd8<C3H/HeJ>/Bmd8<C3H/HeJ>	involves: C3H/HeJ * C57BL/6J	N	14667144
MGI:2679695	F	MP:0001262	decreased body weight	Bmd8<C3H/HeJ>/Bmd8<C3H/HeJ>	involves: C3H/HeJ * C57BL/6J	N	14667144
MGI:2679895	M	MP:0001167	prostate gland epithelial hyperplasia	Pten<tm1Ppp>/Pten<tm2Ppp>	involves: 129S1/Sv * C57BL/6	N	14691534
MGI:2679895	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm1Ppp>/Pten<tm2Ppp>	involves: 129S1/Sv * C57BL/6	N	14691534
MGI:2679895	M	MP:0001158	abnormal prostate gland morphology	Pten<tm1Ppp>/Pten<tm2Ppp>	involves: 129S1/Sv * C57BL/6	N	14691534
MGI:2679895	M	MP:0031369	prostate gland dorsolateral lobe hyperplasia	Pten<tm1Ppp>/Pten<tm2Ppp>	involves: 129S1/Sv * C57BL/6	N	14691534
MGI:2679895	M	MP:0005305	prostate gland anterior lobe hyperplasia	Pten<tm1Ppp>/Pten<tm2Ppp>	involves: 129S1/Sv * C57BL/6	N	14691534
MGI:2679901	M	MP:0001168	abnormal prostate gland epithelium morphology	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	14691534
MGI:2679901	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	28292441
MGI:2679901	M	MP:0001167	prostate gland epithelial hyperplasia	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	14691534
MGI:2679901	M	MP:0001167	prostate gland epithelial hyperplasia	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	16079851
MGI:2679901	M	MP:0001158	abnormal prostate gland morphology	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	14691534
MGI:2679901	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	16079851
MGI:2679901	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	20679199
MGI:2679901	M	MP:0004958	enlarged prostate gland	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	14691534
MGI:2679901	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	14691534
MGI:2679901	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	23817021
MGI:2679901	M	MP:0000659	prostate gland hyperplasia	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	14691534
MGI:2679901	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	16079851
MGI:2679901	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	20679199
MGI:2679901	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	16079851
MGI:2679902	M	MP:0001158	abnormal prostate gland morphology	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)8113ANg/0	involves: 129S1/Sv * C57BL/6	N	14691534
MGI:2679902	M	MP:0004958	enlarged prostate gland	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)8113ANg/0	involves: 129S1/Sv * C57BL/6	N	14691534
MGI:2679902	M	MP:0001167	prostate gland epithelial hyperplasia	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)8113ANg/0	involves: 129S1/Sv * C57BL/6	N	14691534
MGI:2679902	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)8113ANg/0	involves: 129S1/Sv * C57BL/6	N	14691534
MGI:2679917	F	MP:0011645	absent oviduct epithelium motile cilium	Foxj1<tm1Slb>/Foxj1<tm1Slb>	involves: 129X1/SvJ	N	10873152
MGI:2679951	F	MP:0001926	female infertility	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	14561402
MGI:2679951	F	MP:0011122	absent primordial ovarian follicles	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	14561402
MGI:2679951	M	MP:0001925	male infertility	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	14561402
MGI:2679951	M	MP:0005169	abnormal male meiosis	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	14561402
MGI:2679951	M	MP:0001147	small testis	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	14561402
MGI:2679951	M	MP:0001153	small seminiferous tubules	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	14561402
MGI:2679951	M	MP:0001156	abnormal spermatogenesis	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	14561402
MGI:2679951	M	MP:0005159	azoospermia	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	14561402
MGI:2679951	F	MP:0001931	abnormal oogenesis	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	14561402
MGI:2679951	F	MP:0004894	uterus atrophy	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	14561402
MGI:2679951	F	MP:0001126	abnormal ovary morphology	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	14561402
MGI:2679951	F	MP:0004805	absent oocytes	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	14561402
MGI:2679951	F	MP:0004833	ovary atrophy	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	14561402
MGI:2679977	M	MP:0009178	absent pancreatic alpha cells	Arx<tm1Pgr>/Y	involves: 129/Sv * NMRI	N	14561778
MGI:2679977	M	MP:0005218	abnormal pancreatic delta cell morphology	Arx<tm1Pgr>/Y	involves: 129/Sv * NMRI	N	14561778
MGI:2679977	M	MP:0011085	postnatal lethality, complete penetrance	Arx<tm1Pgr>/Y	involves: 129/Sv * NMRI	N	14561778
MGI:2679977	M	MP:0000189	hypoglycemia	Arx<tm1Pgr>/Y	involves: 129/Sv * NMRI	N	14561778
MGI:2679977	M	MP:0003645	increased pancreatic beta cell number	Arx<tm1Pgr>/Y	involves: 129/Sv * NMRI	N	14561778
MGI:2679977	M	MP:0000746	weakness	Arx<tm1Pgr>/Y	involves: 129/Sv * NMRI	N	14561778
MGI:2679977	M	MP:0009180	increased pancreatic delta cell number	Arx<tm1Pgr>/Y	involves: 129/Sv * NMRI	N	14561778
MGI:2679977	M	MP:0001732	postnatal growth retardation	Arx<tm1Pgr>/Y	involves: 129/Sv * NMRI	N	14561778
MGI:2679977	M	MP:0001429	dehydration	Arx<tm1Pgr>/Y	involves: 129/Sv * NMRI	N	14561778
MGI:2680269	F	MP:0000628	abnormal mammary gland development	Erbb4<tm1Fej>/Erbb4<tm1Fej>,Tg(Wap-cre)11738Mam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12954715
MGI:2680269	F	MP:0006270	abnormal mammary gland growth during lactation	Erbb4<tm1Fej>/Erbb4<tm1Fej>,Tg(Wap-cre)11738Mam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12954715
MGI:2680269	F	MP:0001882	abnormal lactation	Erbb4<tm1Fej>/Erbb4<tm1Fej>,Tg(Wap-cre)11738Mam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12954715
MGI:2680289	F	MP:0001663	abnormal digestive system physiology	Tsix<tm1Enl>/Tsix<+>	involves: 129S4/SvJae	N	11262229
MGI:2680291	F	MP:0001698	decreased embryo size	Tsix<tm1Enl>/Tsix<+>,Xist<tm1Jae>/Xist<+>	involves: 129S4/SvJae	N	11262229
MGI:2680456	F	MP:0002628	hepatic steatosis	Pla2g12b<hlb218>/Pla2g12b<hlb218>	C57BL/6J-Pla2g12b<hlb218>/J	N	22912808
MGI:2680668	M	MP:0012307	impaired spatial learning	Foxn1<nu>/Foxn1<nu>	Not Specified	N	15141078
MGI:2680668	F	MP:0001127	small ovary	Foxn1<nu>/Foxn1<nu>	Not Specified	N	5980117
MGI:2680668	M	MP:0001922	reduced male fertility	Foxn1<nu>/Foxn1<nu>	Not Specified	N	5980117
MGI:2680668	F	MP:0001927	abnormal estrous cycle	Foxn1<nu>/Foxn1<nu>	Not Specified	N	5980117
MGI:2680668	F	MP:0001926	female infertility	Foxn1<nu>/Foxn1<nu>	Not Specified	N	5980117
MGI:2680668	M	MP:0009238	coiled sperm flagellum	Foxn1<nu>/Foxn1<nu>	Not Specified	N	5980117
MGI:2680668	M	MP:0002675	asthenozoospermia	Foxn1<nu>/Foxn1<nu>	Not Specified	N	5980117
MGI:2680904	F	MP:0001516	abnormal motor coordination/balance	Abcd1<tm1Kds>/Abcd1<tm1Kds>	involves: 129/Sv * 129S4/SvJae * C57BL/6J	N	11875044
MGI:2680904	F	MP:0001405	impaired coordination	Abcd1<tm1Kds>/Abcd1<tm1Kds>	involves: 129/Sv * 129S4/SvJae * C57BL/6J	N	11875044
MGI:2680904	F	MP:0002757	decreased vertical activity	Abcd1<tm1Kds>/Abcd1<tm1Kds>	involves: 129/Sv * 129S4/SvJae * C57BL/6J	N	11875044
MGI:2680904	F	MP:0005403	abnormal nerve conduction	Abcd1<tm1Kds>/Abcd1<tm1Kds>	involves: 129/Sv * 129S4/SvJae * C57BL/6J	N	11875044
MGI:2680904	F	MP:0001106	abnormal Schwann cell morphology	Abcd1<tm1Kds>/Abcd1<tm1Kds>	involves: 129/Sv * 129S4/SvJae * C57BL/6J	N	11875044
MGI:2680904	F	MP:0005405	axon degeneration	Abcd1<tm1Kds>/Abcd1<tm1Kds>	involves: 129/Sv * 129S4/SvJae * C57BL/6J	N	11875044
MGI:2680904	F	MP:0000920	abnormal myelination	Abcd1<tm1Kds>/Abcd1<tm1Kds>	involves: 129/Sv * 129S4/SvJae * C57BL/6J	N	11875044
MGI:2681092	F	MP:0002080	prenatal lethality	Sta/Sta	Not Specified	N	MGI:61670
MGI:2681093	F	MP:0002075	abnormal coat/hair pigmentation	Sta/Sta<+>	Not Specified	N	MGI:61670
MGI:2681167	M	MP:0020550	multinucleated giant male germ cells	Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0	involves: 129S/Sv * C57BL/6	N	14517263
MGI:2681167	M	MP:0001145	abnormal male reproductive system morphology	Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0	involves: 129S/Sv * C57BL/6	N	14517263
MGI:2681167	F	MP:0001127	small ovary	Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0	involves: 129S/Sv * C57BL/6	N	14517263
MGI:2681167	M	MP:0002216	abnormal seminiferous tubule morphology	Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0	involves: 129S/Sv * C57BL/6	N	14517263
MGI:2681167	F	MP:0001119	abnormal female reproductive system morphology	Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0	involves: 129S/Sv * C57BL/6	N	14517263
MGI:2681167	M	MP:0008261	arrest of male meiosis	Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0	involves: 129S/Sv * C57BL/6	N	14517263
MGI:2681167	F	MP:0002777	absent ovarian follicles	Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0	involves: 129S/Sv * C57BL/6	N	14517263
MGI:2681167	M	MP:0001147	small testis	Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0	involves: 129S/Sv * C57BL/6	N	14517263
MGI:2681494	M	MP:0001940	testis hypoplasia	smk/smk	C57BL/6JY-smk	N	MGI:62197
MGI:2681494	F	MP:0001144	vagina atresia	smk/smk	C57BL/6JY-smk	N	MGI:62197
MGI:2681520	F	MP:0001938	delayed sexual maturation	Ghr<tm1Arge>/Ghr<tm1Arge>	involves: 129S/SvEv * C57BL/6J	N	11133160
MGI:2681522	M	MP:0001155	arrest of spermatogenesis	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	12943692
MGI:2681522	M	MP:0002834	decreased heart weight	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	15961403
MGI:2681522	M	MP:0031633	decreased heart left ventricle muscle contractility	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	15961403
MGI:2681522	M	MP:0005608	cardiac interstitial fibrosis	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	15961403
MGI:2681522	M	MP:0002188	small heart	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	15961403
MGI:2681522	M	MP:0000278	abnormal myocardial fiber morphology	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	15961403
MGI:2681522	M	MP:0001261	obese	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	12943692
MGI:2681522	M	MP:0004565	decreased myocardial fiber size	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	15961403
MGI:2681522	M	MP:0013600	testis degeneration	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	12943692
MGI:2681522	M	MP:0004727	absent epididymis	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	12943692
MGI:2681522	M	MP:0001919	abnormal reproductive system physiology	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	12943692
MGI:2681522	M	MP:0021158	decreased heart left ventricle wall thickness	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	15961403
MGI:2681522	M	MP:0001159	absent prostate gland	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	12943692
MGI:2681522	M	MP:0003921	abnormal heart left ventricle morphology	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	15961403
MGI:2681522	M	MP:0005187	abnormal penis morphology	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	12943692
MGI:2681522	M	MP:0003642	absent seminal vesicle	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	12943692
MGI:2681522	M	MP:0002286	cryptorchism	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	12943692
MGI:2681522	F	MP:0003534	blind vagina	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	12943692
MGI:2681522	M	MP:0003557	absent vas deferens	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	12943692
MGI:2681522	M	MP:0001732	postnatal growth retardation	Ar<tm1Ska>/Y,Tg(CMV-cre)1Ipc/?	involves: C57BL/6 * CBA	N	12943692
MGI:2681789	M	MP:0002673	abnormal sperm number	S100a11<tm1Wen>/S100a11<tm1Wen>	involves: 129	N	14579419
MGI:2682002	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	N	14612522
MGI:2682002	M	MP:0009592	increased Leydig cell tumor incidence	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	N	14612522
MGI:2682595	M	MP:0002687	oligozoospermia	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	N	14585983
MGI:2682595	F	MP:0013504	increased embryonic tissue cell apoptosis	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	N	14585983
MGI:2682595	M	MP:0001925	male infertility	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	N	14585983
MGI:2682595	M	MP:0013600	testis degeneration	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	N	14585983
MGI:2682595	F	MP:0011101	prenatal lethality, incomplete penetrance	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	N	14585983
MGI:2682595	F	MP:0008932	abnormal embryonic tissue physiology	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	N	14585983
MGI:2682595	F	MP:0001923	reduced female fertility	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	N	14585983
MGI:2682595	F	MP:0002085	abnormal embryonic tissue morphology	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	N	14585983
MGI:2682595	M	MP:0008261	arrest of male meiosis	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	N	14585983
MGI:2682595	F	MP:0001732	postnatal growth retardation	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	N	14585983
MGI:2682597	M	MP:0013600	testis degeneration	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * CD-1	N	14585983
MGI:2682598	M	MP:0013600	testis degeneration	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv	N	14585983
MGI:2682626	M	MP:0001925	male infertility	Nanos2<tm1Ysa>/Nanos2<tm1Ysa>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	12947200
MGI:2682626	M	MP:0005159	azoospermia	Nanos2<tm1Ysa>/Nanos2<tm1Ysa>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	12947200
MGI:2682626	M	MP:0004852	decreased testis weight	Nanos2<tm1Ysa>/Nanos2<tm1Ysa>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	12947200
MGI:2682627	F	MP:0001926	female infertility	Nanos3<tm1Ysa>/Nanos3<tm1Ysa>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	12947200
MGI:2682627	M	MP:0005159	azoospermia	Nanos3<tm1Ysa>/Nanos3<tm1Ysa>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	12947200
MGI:2682627	F	MP:0001127	small ovary	Nanos3<tm1Ysa>/Nanos3<tm1Ysa>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	12947200
MGI:2682627	M	MP:0004852	decreased testis weight	Nanos3<tm1Ysa>/Nanos3<tm1Ysa>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	12947200
MGI:2682627	M	MP:0001925	male infertility	Nanos3<tm1Ysa>/Nanos3<tm1Ysa>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	12947200
MGI:2682666	F	MP:0002100	abnormal tooth morphology	Sox3<tm1.1Lja>/Sox3<tm1.1Lja>	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682666	F	MP:0005386	behavior/neurological phenotype	Sox3<tm1.1Lja>/Sox3<tm1.1Lja>	involves: 129S1/Sv * 129X1/SvJ	Y	14585968
MGI:2682666	F	MP:0001130	abnormal ovarian folliculogenesis	Sox3<tm1.1Lja>/Sox3<tm1.1Lja>	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682666	F	MP:0001923	reduced female fertility	Sox3<tm1.1Lja>/Sox3<tm1.1Lja>	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682666	F	MP:0001262	decreased body weight	Sox3<tm1.1Lja>/Sox3<tm1.1Lja>	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682666	F	MP:0031239	increased atretic ovarian follicle number	Sox3<tm1.1Lja>/Sox3<tm1.1Lja>	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682666	F	MP:0001125	abnormal oocyte morphology	Sox3<tm1.1Lja>/Sox3<tm1.1Lja>	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682666	F	MP:0001119	abnormal female reproductive system morphology	Sox3<tm1.1Lja>/Sox3<tm1.1Lja>	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682795	M	MP:0001156	abnormal spermatogenesis	Sox3<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682795	M	MP:0002209	decreased germ cell number	Sox3<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682795	M	MP:0002100	abnormal tooth morphology	Sox3<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682795	M	MP:0002784	abnormal Sertoli cell morphology	Sox3<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682795	M	MP:0002216	abnormal seminiferous tubule morphology	Sox3<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682795	M	MP:0001262	decreased body weight	Sox3<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682795	M	MP:0002687	oligozoospermia	Sox3<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682795	M	MP:0004852	decreased testis weight	Sox3<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	N	14585968
MGI:2682795	M	MP:0005386	behavior/neurological phenotype	Sox3<tm1.1Lja>/Y	involves: 129S1/Sv * 129X1/SvJ	Y	14585968
MGI:2682804	F	MP:0031434	increased miscarriage rate	Slc13a1<tm1Mark>/Slc13a1<tm1Mark>	involves: 129T2/SvEms * C57BL/6J	N	14578452
MGI:2682804	F	MP:0001923	reduced female fertility	Slc13a1<tm1Mark>/Slc13a1<tm1Mark>	involves: 129T2/SvEms * C57BL/6J	N	14578452
MGI:2682910	M	MP:0001463	abnormal spatial learning	L1cam<tm1Fmo>/Y,Tg(Camk2a-cre)1Gsc/0	involves: 129/Sv * C57BL/6	N	14614101
MGI:2682910	M	MP:0001364	decreased anxiety-related response	L1cam<tm1Fmo>/Y,Tg(Camk2a-cre)1Gsc/0	involves: 129/Sv * C57BL/6	N	14614101
MGI:2682910	M	MP:0001415	increased exploration in new environment	L1cam<tm1Fmo>/Y,Tg(Camk2a-cre)1Gsc/0	involves: 129/Sv * C57BL/6	N	14614101
MGI:2682910	M	MP:0001399	hyperactivity	L1cam<tm1Fmo>/Y,Tg(Camk2a-cre)1Gsc/0	involves: 129/Sv * C57BL/6	N	14614101
MGI:2682910	M	MP:0002574	increased vertical activity	L1cam<tm1Fmo>/Y,Tg(Camk2a-cre)1Gsc/0	involves: 129/Sv * C57BL/6	N	14614101
MGI:2682910	M	MP:0002206	abnormal CNS synaptic transmission	L1cam<tm1Fmo>/Y,Tg(Camk2a-cre)1Gsc/0	involves: 129/Sv * C57BL/6	N	14614101
MGI:2682916	M	MP:0001922	reduced male fertility	H3f3a<Gt(ROSABetageo)14E7Ev>/H3f3a<Gt(ROSABetageo)14E7Ev>	involves: 129	N	10362650
MGI:2682916	F	MP:0001923	reduced female fertility	H3f3a<Gt(ROSABetageo)14E7Ev>/H3f3a<Gt(ROSABetageo)14E7Ev>	involves: 129	N	10362650
MGI:2682957	F	MP:0001125	abnormal oocyte morphology	Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>	Not Specified	N	11912493
MGI:2682957	F	MP:0001926	female infertility	Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>	Not Specified	N	11912493
MGI:2682957	F	MP:0005168	abnormal female meiosis	Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>	Not Specified	N	11912493
MGI:2683289	F	MP:0005431	decreased oocyte number	Pepd<dal>/Pepd<dal>	CBA/J-Pepd<dal>/GrsrJ	N	MGI:2682797
MGI:2683624	M	MP:0005159	azoospermia	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	N	13129914
MGI:2683624	M	MP:0001925	male infertility	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	N	13129914
MGI:2683624	M	MP:0001147	small testis	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	N	13129914
MGI:2683624	M	MP:0006380	abnormal spermatid morphology	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	N	13129914
MGI:2683624	M	MP:0008898	abnormal acrosome morphology	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	N	13129914
MGI:2683624	M	MP:0002216	abnormal seminiferous tubule morphology	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	N	13129914
MGI:2683624	M	MP:0008279	arrest of spermiogenesis	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	N	13129914
MGI:2683624	M	MP:0001932	abnormal spermiogenesis	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	N	13129914
MGI:2683624	M	MP:0006378	abnormal spermatogonia morphology	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	N	13129914
MGI:2683624	M	MP:0001146	abnormal testis morphology	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	N	13129914
MGI:2683624	M	MP:0004182	abnormal spermiation	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	N	13129914
MGI:2683698	F	MP:0009503	abnormal mammary gland duct morphology	Becn1<tm1Blev>/Becn1<+>	involves: 129X1/SvJ * C57BL/6J	N	14638851
MGI:2683730	F	MP:0001926	female infertility	Dppa3<tm1Masu>/Dppa3<tm1Masu>	involves: 129S/SvEv	N	14654002
MGI:2683846	M	MP:0001925	male infertility	Catsper2<tm1Gar>/Catsper2<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6J	N	14657366
MGI:2683846	M	MP:0030976	impaired sperm penetration of zona pellucida	Catsper2<tm1Gar>/Catsper2<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6J	N	14657366
MGI:2683846	M	MP:0002675	asthenozoospermia	Catsper2<tm1Gar>/Catsper2<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6J	N	14657366
MGI:2683994	F	MP:0005385	cardiovascular system phenotype	Ada<tm1Mw>/Ada<tm1Mw>,Tg(PLADA)4118Rkmb/0	involves: 129S7/SvEvBrd * C57BL/6	Y	25538227
MGI:2683994	F	MP:0005367	renal/urinary system phenotype	Ada<tm1Mw>/Ada<tm1Mw>,Tg(PLADA)4118Rkmb/0	involves: 129S7/SvEvBrd * C57BL/6	Y	25538227
MGI:2683994	F	MP:0005380	embryo phenotype	Ada<tm1Mw>/Ada<tm1Mw>,Tg(PLADA)4118Rkmb/0	involves: 129S7/SvEvBrd * C57BL/6	Y	25538227
MGI:2684062	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	N	11884614
MGI:2684062	M	MP:0005159	azoospermia	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	N	11884614
MGI:2684062	M	MP:0008261	arrest of male meiosis	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	N	11884614
MGI:2684062	M	MP:0001147	small testis	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	N	11884614
MGI:2684062	F	MP:0001923	reduced female fertility	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	N	11884614
MGI:2684062	M	MP:0001925	male infertility	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	N	11884614
MGI:2684062	M	MP:0002216	abnormal seminiferous tubule morphology	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	N	11884614
MGI:2684062	M	MP:0001156	abnormal spermatogenesis	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	N	11884614
MGI:2684289	M	MP:0009836	abnormal sperm principal piece morphology	Akap4<tm1Eddy>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12167408
MGI:2684289	M	MP:0009282	decreased hyperactivated sperm motility	Akap4<tm1Eddy>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12167408
MGI:2684289	M	MP:0009837	abnormal sperm end piece morphology	Akap4<tm1Eddy>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12167408
MGI:2684289	M	MP:0001925	male infertility	Akap4<tm1Eddy>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12167408
MGI:2684289	M	MP:0009239	short sperm flagellum	Akap4<tm1Eddy>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12167408
MGI:2684289	M	MP:0009238	coiled sperm flagellum	Akap4<tm1Eddy>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12167408
MGI:2684289	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Akap4<tm1Eddy>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12167408
MGI:2684289	M	MP:0009280	decreased activated sperm motility	Akap4<tm1Eddy>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12167408
MGI:2684289	M	MP:0004543	abnormal sperm physiology	Akap4<tm1Eddy>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12167408
MGI:2684289	M	MP:0008892	abnormal sperm flagellum morphology	Akap4<tm1Eddy>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12167408
MGI:2684290	F	MP:0005389	reproductive system phenotype	Akap4<tm1Eddy>/Akap4<+>	involves: 129S6/SvEvTac * C57BL/6	Y	12167408
MGI:2684306	F	MP:0008028	pregnancy-related premature death	F13a1<tm1Gdi>/F13a1<tm1Gdi>	involves: 129P2/OlaHsd * CBA/Ca	N	12529747
MGI:2684306	F	MP:0009661	abnormal pregnancy	F13a1<tm1Gdi>/F13a1<tm1Gdi>	involves: 129P2/OlaHsd * CBA/Ca	N	12529747
MGI:2684307	F	MP:0004898	uterine hemorrhage	F13a1<tm1Gdi>/F13a1<tm1Gdi>	involves: 129P2/OlaHsd	N	12933578
MGI:2684307	F	MP:0008028	pregnancy-related premature death	F13a1<tm1Gdi>/F13a1<tm1Gdi>	involves: 129P2/OlaHsd	N	12933578
MGI:2684307	F	MP:0001923	reduced female fertility	F13a1<tm1Gdi>/F13a1<tm1Gdi>	involves: 129P2/OlaHsd	N	12933578
MGI:2684408	M	MP:0009808	decreased oligodendrocyte number	Plp1<jp>/Y	B6CB-A<w-J>/A Eda<Ta> Plp1<jp>	N	1206429
MGI:2684408	M	MP:0000920	abnormal myelination	Plp1<jp>/Y	B6CB-A<w-J>/A Eda<Ta> Plp1<jp>	N	1206429
MGI:2684408	M	MP:0000953	abnormal oligodendrocyte morphology	Plp1<jp>/Y	B6CB-A<w-J>/A Eda<Ta> Plp1<jp>	N	1206429
MGI:2684408	M	MP:0001290	delayed eyelid opening	Plp1<jp>/Y	B6CB-A<w-J>/A Eda<Ta> Plp1<jp>	N	8187967
MGI:2684408	M	MP:0001402	decreased locomotor activity	Plp1<jp>/Y	B6CB-A<w-J>/A Eda<Ta> Plp1<jp>	N	8187967
MGI:2684408	M	MP:0001262	decreased body weight	Plp1<jp>/Y	B6CB-A<w-J>/A Eda<Ta> Plp1<jp>	N	8187967
MGI:2684408	M	MP:0020351	decreased vocalization	Plp1<jp>/Y	B6CB-A<w-J>/A Eda<Ta> Plp1<jp>	N	8187967
MGI:2684408	M	MP:0008916	abnormal astrocyte physiology	Plp1<jp>/Y	B6CB-A<w-J>/A Eda<Ta> Plp1<jp>	N	8269866
MGI:2684408	M	MP:0001486	abnormal startle reflex	Plp1<jp>/Y	B6CB-A<w-J>/A Eda<Ta> Plp1<jp>	N	8187967
MGI:2684408	M	MP:0000920	abnormal myelination	Plp1<jp>/Y	B6CB-A<w-J>/A Eda<Ta> Plp1<jp>	N	2051161
MGI:2684460	F	MP:0003354	astrocytosis	Plp1<jp>/Plp1<+>	B6CB-A<w-J>/A Eda<Ta> Plp1<jp>	N	6291720
MGI:2684641	F	MP:0001259	abnormal body weight	Fnld/Fnld<+>	(C3H/HeH x 101/H)F1	N	10036977
MGI:2684641	F	MP:0011101	prenatal lethality, incomplete penetrance	Fnld/Fnld<+>	(C3H/HeH x 101/H)F1	N	10036977
MGI:2684641	F	MP:0000367	abnormal coat/ hair morphology	Fnld/Fnld<+>	(C3H/HeH x 101/H)F1	N	10036977
MGI:2684643	M	MP:0011099	lethality throughout fetal growth and development, complete penetrance	Fnld/Y	(C3H/HeH x 101/H)F1	N	10036977
MGI:2684661	M	MP:0001925	male infertility	Reln<rl>/Reln<rl>	Not Specified	N	24539699
MGI:2684661	F	MP:0001923	reduced female fertility	Reln<rl>/Reln<rl>	Not Specified	N	24539699
MGI:2686668	F	MP:0001386	abnormal maternal nurturing	Naq1<RR>/Naq1<RR>	involves: KK * RR	N	11869186
MGI:2686668	F	MP:0001386	abnormal maternal nurturing	Naq1<RR>/Naq1<RR>	involves: KK * RR	N	15472464
MGI:2686840	F	MP:0011091	prenatal lethality, complete penetrance	Flna<Dilp2>/Flna<Dilp2>	involves: BALB/cAnN * C3H/HeN	N	11929848
MGI:2686842	M	MP:0011091	prenatal lethality, complete penetrance	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN	N	11929848
MGI:2686843	F	MP:0002092	abnormal eye morphology	Flna<Dilp2>/Flna<+>	involves: BALB/cAnN * C3H/HeN	N	11929848
MGI:2686843	F	MP:0002546	mydriasis	Flna<Dilp2>/Flna<+>	involves: BALB/cAnN * C3H/HeN	N	11929848
MGI:2687004	M	MP:0002687	oligozoospermia	Abca1<tm1Jdm>/Abca1<tm1Jdm>	involves: DBA/1LacJ	N	15026428
MGI:2687004	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Abca1<tm1Jdm>/Abca1<tm1Jdm>	involves: DBA/1LacJ	N	15026428
MGI:2687004	M	MP:0011385	abnormal testosterone level	Abca1<tm1Jdm>/Abca1<tm1Jdm>	involves: DBA/1LacJ	N	15026428
MGI:2687004	M	MP:0000186	decreased circulating HDL cholesterol level	Abca1<tm1Jdm>/Abca1<tm1Jdm>	involves: DBA/1LacJ	N	15026428
MGI:2687004	M	MP:0002216	abnormal seminiferous tubule morphology	Abca1<tm1Jdm>/Abca1<tm1Jdm>	involves: DBA/1LacJ	N	15026428
MGI:2687004	M	MP:0002786	abnormal Leydig cell morphology	Abca1<tm1Jdm>/Abca1<tm1Jdm>	involves: DBA/1LacJ	N	15026428
MGI:2687004	M	MP:0005278	abnormal cholesterol homeostasis	Abca1<tm1Jdm>/Abca1<tm1Jdm>	involves: DBA/1LacJ	N	15026428
MGI:2687004	M	MP:0003193	decreased cholesterol efflux	Abca1<tm1Jdm>/Abca1<tm1Jdm>	involves: DBA/1LacJ	N	15026428
MGI:2687004	M	MP:0002784	abnormal Sertoli cell morphology	Abca1<tm1Jdm>/Abca1<tm1Jdm>	involves: DBA/1LacJ	N	15026428
MGI:2687004	M	MP:0001154	seminiferous tubule degeneration	Abca1<tm1Jdm>/Abca1<tm1Jdm>	involves: DBA/1LacJ	N	15026428
MGI:2687004	M	MP:0001922	reduced male fertility	Abca1<tm1Jdm>/Abca1<tm1Jdm>	involves: DBA/1LacJ	N	15026428
MGI:2687079	M	MP:0002286	cryptorchism	Epha4<rb>/Epha4<rb>	B6 x STOCK Epha4<rb>/J	N	MGI:2684201
MGI:2687079	M	MP:0001922	reduced male fertility	Epha4<rb>/Epha4<rb>	B6 x STOCK Epha4<rb>/J	N	MGI:2684201
MGI:2687080	F	MP:0001386	abnormal maternal nurturing	Epha4<rb-2J>/Epha4<rb-2J>	C57BL/6J-Epha4<rb-2J>/GrsrJ	N	MGI:2684201
MGI:2687080	M	MP:0002286	cryptorchism	Epha4<rb-2J>/Epha4<rb-2J>	C57BL/6J-Epha4<rb-2J>/GrsrJ	N	MGI:2684201
MGI:2687080	M	MP:0001922	reduced male fertility	Epha4<rb-2J>/Epha4<rb-2J>	C57BL/6J-Epha4<rb-2J>/GrsrJ	N	MGI:2684201
MGI:3026668	F	MP:0001353	increased aggression towards mice	Aggr2<NZB/BlNJ>/Aggr2<NZB/BlNJ>	involves: A/J * NZB/BlNJ	N	11826145
MGI:3026669	F	MP:0001353	increased aggression towards mice	Aggr2<A/J>/Aggr2<NZB/BlNJ>	involves: A/J * NZB/BlNJ	N	11826145
MGI:3026716	M	MP:0001925	male infertility	inft2/inft2	Not Specified	N	12955145
MGI:3026717	F	MP:0001926	female infertility	inft3/inft3	Not Specified	N	12955145
MGI:3026718	M	MP:0002686	globozoospermia	inft4/inft4	Not Specified	N	14711786
MGI:3026718	M	MP:0001155	arrest of spermatogenesis	inft4/inft4	Not Specified	N	14711786
MGI:3026718	M	MP:0002687	oligozoospermia	inft4/inft4	Not Specified	N	14711786
MGI:3026718	M	MP:0001925	male infertility	inft4/inft4	Not Specified	N	12955145
MGI:3026718	M	MP:0001155	arrest of spermatogenesis	inft4/inft4	Not Specified	N	12955145
MGI:3026718	M	MP:0020451	decreased sperm progressive motility	inft4/inft4	Not Specified	N	14711786
MGI:3026718	M	MP:0009239	short sperm flagellum	inft4/inft4	Not Specified	N	14711786
MGI:3026719	M	MP:0001925	male infertility	inft5/inft5	Not Specified	N	12955145
MGI:3026720	M	MP:0001922	reduced male fertility	inft6/inft6	Not Specified	N	12955145
MGI:3026721	F	MP:0001926	female infertility	inft7/inft7	Not Specified	N	12955145
MGI:3026722	M	MP:0002687	oligozoospermia	inft8/inft8	Not Specified	N	14711786
MGI:3026722	M	MP:0001155	arrest of spermatogenesis	inft8/inft8	Not Specified	N	14711786
MGI:3026722	M	MP:0001155	arrest of spermatogenesis	inft8/inft8	Not Specified	N	12955145
MGI:3026722	M	MP:0002686	globozoospermia	inft8/inft8	Not Specified	N	14711786
MGI:3026722	M	MP:0008892	abnormal sperm flagellum morphology	inft8/inft8	Not Specified	N	14711786
MGI:3026722	M	MP:0001925	male infertility	inft8/inft8	Not Specified	N	12955145
MGI:3026722	M	MP:0020451	decreased sperm progressive motility	inft8/inft8	Not Specified	N	14711786
MGI:3026723	M	MP:0001155	arrest of spermatogenesis	inft9/inft9	Not Specified	N	12955145
MGI:3026723	M	MP:0008892	abnormal sperm flagellum morphology	inft9/inft9	Not Specified	N	14711786
MGI:3026723	M	MP:0001155	arrest of spermatogenesis	inft9/inft9	Not Specified	N	14711786
MGI:3026723	M	MP:0002686	globozoospermia	inft9/inft9	Not Specified	N	14711786
MGI:3026723	M	MP:0002687	oligozoospermia	inft9/inft9	Not Specified	N	14711786
MGI:3026723	M	MP:0020451	decreased sperm progressive motility	inft9/inft9	Not Specified	N	14711786
MGI:3026723	M	MP:0001925	male infertility	inft9/inft9	Not Specified	N	12955145
MGI:3026859	F	MP:0003570	increased uterus leiomyoma incidence	Htatip2<tm1Hx>/Htatip2<tm1Hx>	involves: 129P2/OlaHsd * C57BL/6J	N	14695192
MGI:3026859	F	MP:0000627	abnormal mammary gland morphology	Htatip2<tm1Hx>/Htatip2<tm1Hx>	involves: 129P2/OlaHsd * C57BL/6J	N	14695192
MGI:3026867	F	MP:0014127	increased thymoma incidence	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	14695192
MGI:3026867	F	MP:0008000	increased ovary tumor incidence	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	14695192
MGI:3027033	M	MP:0001925	male infertility	Dhcr24<tm1Lex>/Dhcr24<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	14684813
MGI:3027033	F	MP:0001926	female infertility	Dhcr24<tm1Lex>/Dhcr24<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	14684813
MGI:3027033	M	MP:0013600	testis degeneration	Dhcr24<tm1Lex>/Dhcr24<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	14684813
MGI:3027041	F	MP:0001923	reduced female fertility	Mre11a<tm1Jpt>/Mre11a<tm1Jpt>	involves: 129S7/SvEvBrd * C57BL/6	N	14690604
MGI:3027146	M	MP:0006262	increased testis tumor incidence	Pgct1<129S1/SvImJ>/?	involves: 129S1/SvImJ * C57BL/6J	N	10890890
MGI:3027504	F	MP:0004906	enlarged uterus	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	N	14729625
MGI:3027504	F	MP:0001923	reduced female fertility	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	N	14729625
MGI:3027504	F	MP:0009094	abnormal endometrial gland morphology	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	N	14729625
MGI:3027504	F	MP:0001123	dilated uterus	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	N	14729625
MGI:3027504	F	MP:0009092	endometrium hyperplasia	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	N	14729625
MGI:3027504	F	MP:0004896	abnormal endometrium morphology	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	N	14729625
MGI:3027504	F	MP:0004868	increased endometrial carcinoma incidence	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	N	14729625
MGI:3027726	M	MP:0000665	decreased ductal branching in the coagulating gland	Nkx3-1<tm1Siz>/Nkx3-1<tm1Siz>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11002344
MGI:3027726	M	MP:0001168	abnormal prostate gland epithelium morphology	Nkx3-1<tm1Siz>/Nkx3-1<tm1Siz>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11002344
MGI:3027726	M	MP:0000664	small prostate gland anterior lobe	Nkx3-1<tm1Siz>/Nkx3-1<tm1Siz>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11002344
MGI:3027726	M	MP:0001167	prostate gland epithelial hyperplasia	Nkx3-1<tm1Siz>/Nkx3-1<tm1Siz>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11002344
MGI:3027726	M	MP:0000666	decreased prostate gland duct number	Nkx3-1<tm1Siz>/Nkx3-1<tm1Siz>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11002344
MGI:3027726	M	MP:0001163	abnormal prostate gland anterior lobe morphology	Nkx3-1<tm1Siz>/Nkx3-1<tm1Siz>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11002344
MGI:3027726	M	MP:0001157	small seminal vesicle	Nkx3-1<tm1Siz>/Nkx3-1<tm1Siz>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11002344
MGI:3027726	M	MP:0000660	prostate gland lateral lobe hypoplasia	Nkx3-1<tm1Siz>/Nkx3-1<tm1Siz>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11002344
MGI:3027726	M	MP:0000661	small prostate gland ventral lobe	Nkx3-1<tm1Siz>/Nkx3-1<tm1Siz>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11002344
MGI:3027726	M	MP:0001158	abnormal prostate gland morphology	Nkx3-1<tm1Siz>/Nkx3-1<tm1Siz>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11002344
MGI:3027822	F	MP:0031420	decreased superovulation rate	Mst1r<tm1.1Sew>/Mst1r<tm1.1Sew>	involves: 129/Ola * CD-1 * NIH Black Swiss	N	14505749
MGI:3027822	F	MP:0001127	small ovary	Mst1r<tm1.1Sew>/Mst1r<tm1.1Sew>	involves: 129/Ola * CD-1 * NIH Black Swiss	N	11518730
MGI:3027822	F	MP:0001126	abnormal ovary morphology	Mst1r<tm1.1Sew>/Mst1r<tm1.1Sew>	involves: 129/Ola * CD-1 * NIH Black Swiss	N	11518730
MGI:3027861	M	MP:0002286	cryptorchism	ww1/ww1	Not Specified	N	12955145
MGI:3027900	F	MP:0001926	female infertility	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	N	11106738
MGI:3027900	M	MP:0002216	abnormal seminiferous tubule morphology	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	N	11106738
MGI:3027900	M	MP:0001156	abnormal spermatogenesis	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	N	11106738
MGI:3027900	M	MP:0001145	abnormal male reproductive system morphology	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	N	11106738
MGI:3027900	M	MP:0001925	male infertility	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	N	11106738
MGI:3027900	F	MP:0001126	abnormal ovary morphology	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	N	11106738
MGI:3027900	F	MP:0005168	abnormal female meiosis	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	N	11106738
MGI:3027900	M	MP:0001147	small testis	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	N	11106738
MGI:3027900	F	MP:0001119	abnormal female reproductive system morphology	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	N	11106738
MGI:3027900	M	MP:0005169	abnormal male meiosis	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	N	23318132
MGI:3027900	M	MP:0008261	arrest of male meiosis	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	N	11106738
MGI:3027936	M	MP:0003205	testicular atrophy	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ	N	19339492
MGI:3027936	M	MP:0002687	oligozoospermia	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ	N	19339492
MGI:3027936	M	MP:0004852	decreased testis weight	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ	N	19339492
MGI:3028332	F	MP:0001868	ovary inflammation	Aod1a<A/J>/?	involves: A/J * C57BL/6J	N	12794114
MGI:3028333	F	MP:0001868	ovary inflammation	Aod1b<C57BL/6J>/?	involves: A/J * C57BL/6J	N	12794114
MGI:3028422	F	MP:0002223	lymphoid hypoplasia	Was<tm1Kas>/Was<tm1Kas>	involves: 129/Sv * C57BL/6	N	10544204
MGI:3028422	F	MP:0005018	decreased T cell number	Was<tm1Kas>/Was<tm1Kas>	involves: 129/Sv * C57BL/6	N	10544204
MGI:3028422	F	MP:0003179	thrombocytopenia	Was<tm1Kas>/Was<tm1Kas>	involves: 129/Sv * C57BL/6	N	10544204
MGI:3028422	F	MP:0005016	decreased lymphocyte cell number	Was<tm1Kas>/Was<tm1Kas>	involves: 129/Sv * C57BL/6	N	10544204
MGI:3028422	F	MP:0005092	decreased double-positive T cell number	Was<tm1Kas>/Was<tm1Kas>	involves: 129/Sv * C57BL/6	N	10544204
MGI:3028422	F	MP:0001823	thymus hypoplasia	Was<tm1Kas>/Was<tm1Kas>	involves: 129/Sv * C57BL/6	N	10544204
MGI:3028422	F	MP:0005017	decreased B cell number	Was<tm1Kas>/Was<tm1Kas>	involves: 129/Sv * C57BL/6	N	10544204
MGI:3028689	M	MP:0001145	abnormal male reproductive system morphology	Rxfp1<tm1Jgo>/Rxfp1<tm1Jgo>	involves: 129S5/SvEvBrd * C57BL/6	N	14701741
MGI:3028689	M	MP:0004852	decreased testis weight	Rxfp1<tm1Jgo>/Rxfp1<tm1Jgo>	involves: 129S5/SvEvBrd * C57BL/6	N	14701741
MGI:3028689	M	MP:0001922	reduced male fertility	Rxfp1<tm1Jgo>/Rxfp1<tm1Jgo>	involves: 129S5/SvEvBrd * C57BL/6	N	14701741
MGI:3028689	M	MP:0001156	abnormal spermatogenesis	Rxfp1<tm1Jgo>/Rxfp1<tm1Jgo>	involves: 129S5/SvEvBrd * C57BL/6	N	14701741
MGI:3028689	F	MP:0001119	abnormal female reproductive system morphology	Rxfp1<tm1Jgo>/Rxfp1<tm1Jgo>	involves: 129S5/SvEvBrd * C57BL/6	N	14701741
MGI:3028689	M	MP:0004929	decreased epididymis weight	Rxfp1<tm1Jgo>/Rxfp1<tm1Jgo>	involves: 129S5/SvEvBrd * C57BL/6	N	14701741
MGI:3028689	F	MP:0013713	decreased nipple size	Rxfp1<tm1Jgo>/Rxfp1<tm1Jgo>	involves: 129S5/SvEvBrd * C57BL/6	N	14701741
MGI:3028689	F	MP:0002907	abnormal parturition	Rxfp1<tm1Jgo>/Rxfp1<tm1Jgo>	involves: 129S5/SvEvBrd * C57BL/6	N	14701741
MGI:3028689	M	MP:0005159	azoospermia	Rxfp1<tm1Jgo>/Rxfp1<tm1Jgo>	involves: 129S5/SvEvBrd * C57BL/6	N	14701741
MGI:3028689	F	MP:0001923	reduced female fertility	Rxfp1<tm1Jgo>/Rxfp1<tm1Jgo>	involves: 129S5/SvEvBrd * C57BL/6	N	14701741
MGI:3028763	M	MP:0005578	teratozoospermia	Smpd1<tm1Esc>/Smpd1<tm1Esc>	involves: 129S1/Sv * C57BL/6J	N	12213735
MGI:3028763	M	MP:0002675	asthenozoospermia	Smpd1<tm1Esc>/Smpd1<tm1Esc>	involves: 129S1/Sv * C57BL/6J	N	12213735
MGI:3028763	M	MP:0003666	impaired sperm capacitation	Smpd1<tm1Esc>/Smpd1<tm1Esc>	involves: 129S1/Sv * C57BL/6J	N	12213735
MGI:3028763	M	MP:0006362	abnormal male germ cell morphology	Smpd1<tm1Esc>/Smpd1<tm1Esc>	involves: 129S1/Sv * C57BL/6J	N	12213735
MGI:3028846	M	MP:0006379	abnormal spermatocyte morphology	Del(17Hspa1b-Hsp1a)1Dix/Del(17Hspa1b-Hsp1a)1Dix	involves: 129S7/SvEvBrd	N	14701760
MGI:3028877	M	MP:0005387	immune system phenotype	Elk1<tm1Nor>/Y	involves: 129P2/OlaHsd * C57BL/6N	Y	14673163
MGI:3028877	M	MP:0002675	asthenozoospermia	Elk1<tm1Nor>/Y	involves: 129P2/OlaHsd * C57BL/6N	N	14994271
MGI:3028877	M	MP:0001925	male infertility	Elk1<tm1Nor>/Y	involves: 129P2/OlaHsd * C57BL/6N	N	14673163
MGI:3028877	M	MP:0003631	nervous system phenotype	Elk1<tm1Nor>/Y	involves: 129P2/OlaHsd * C57BL/6N	Y	14673163
MGI:3028887	F	MP:0002460	decreased immunoglobulin level	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	11104803
MGI:3028887	F	MP:0005093	decreased B cell proliferation	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	11104803
MGI:3028887	F	MP:0001806	decreased IgM level	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	11104803
MGI:3028887	F	MP:0005464	abnormal platelet physiology	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	12842985
MGI:3028887	F	MP:0005017	decreased B cell number	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	11104803
MGI:3028887	F	MP:0002144	abnormal B cell differentiation	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	11104803
MGI:3028887	F	MP:0009549	decreased platelet aggregation	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	12842985
MGI:3028887	F	MP:0002357	abnormal spleen white pulp morphology	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	11104803
MGI:3028887	F	MP:0002362	abnormal spleen marginal zone morphology	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	11104803
MGI:3028887	F	MP:0008498	decreased IgG3 level	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	11104803
MGI:3028887	F	MP:0008496	decreased IgG2a level	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	11104803
MGI:3028887	F	MP:0003132	increased pre-B cell number	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	11104803
MGI:3028887	F	MP:0001800	abnormal humoral immune response	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	11104803
MGI:3028887	F	MP:0000689	abnormal spleen morphology	Btk<tm1Wk>/Btk<tm1Wk>,Tec<tm1Welm>/Tec<tm1Welm>	involves: 129P2/OlaHsd * C57BL/6	N	11104803
MGI:3028977	F	MP:0001931	abnormal oogenesis	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9660954
MGI:3028977	M	MP:0005159	azoospermia	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9660954
MGI:3028977	F	MP:0004805	absent oocytes	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9660954
MGI:3028977	M	MP:0008261	arrest of male meiosis	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9660954
MGI:3028977	M	MP:0001156	abnormal spermatogenesis	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9660954
MGI:3028977	M	MP:0001147	small testis	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9660954
MGI:3028977	M	MP:0001925	male infertility	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9660954
MGI:3028977	F	MP:0002777	absent ovarian follicles	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9660954
MGI:3028977	F	MP:0001127	small ovary	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9660954
MGI:3029001	M	MP:0001711	abnormal placenta morphology	Cited1<tm1Dunw>/Y	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029001	M	MP:0002086	abnormal extraembryonic tissue morphology	Cited1<tm1Dunw>/Y	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029001	M	MP:0003231	abnormal placenta vasculature	Cited1<tm1Dunw>/Y	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029001	M	MP:0011521	decreased placental labyrinth size	Cited1<tm1Dunw>/Y	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029001	M	MP:0009431	decreased fetal weight	Cited1<tm1Dunw>/Y	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029001	M	MP:0011088	neonatal lethality, incomplete penetrance	Cited1<tm1Dunw>/Y	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029001	M	MP:0009674	decreased birth weight	Cited1<tm1Dunw>/Y	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029001	M	MP:0011527	disorganized placental labyrinth	Cited1<tm1Dunw>/Y	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029001	M	MP:0012098	increased spongiotrophoblast size	Cited1<tm1Dunw>/Y	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029001	M	MP:0008803	abnormal placental labyrinth vasculature morphology	Cited1<tm1Dunw>/Y	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029002	F	MP:0009674	decreased birth weight	Cited1<tm1Dunw>/Cited1<tm1Dunw>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029002	F	MP:0001711	abnormal placenta morphology	Cited1<tm1Dunw>/Cited1<tm1Dunw>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029002	F	MP:0011088	neonatal lethality, incomplete penetrance	Cited1<tm1Dunw>/Cited1<tm1Dunw>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029002	F	MP:0003231	abnormal placenta vasculature	Cited1<tm1Dunw>/Cited1<tm1Dunw>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029002	F	MP:0009431	decreased fetal weight	Cited1<tm1Dunw>/Cited1<tm1Dunw>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029002	F	MP:0002086	abnormal extraembryonic tissue morphology	Cited1<tm1Dunw>/Cited1<tm1Dunw>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/10 * CBA	N	14673158
MGI:3029003	M	MP:0011521	decreased placental labyrinth size	Cited1<tm1Dunw>/Y	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029003	M	MP:0009431	decreased fetal weight	Cited1<tm1Dunw>/Y	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029003	M	MP:0003231	abnormal placenta vasculature	Cited1<tm1Dunw>/Y	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029003	M	MP:0002086	abnormal extraembryonic tissue morphology	Cited1<tm1Dunw>/Y	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029003	M	MP:0001711	abnormal placenta morphology	Cited1<tm1Dunw>/Y	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029003	M	MP:0008803	abnormal placental labyrinth vasculature morphology	Cited1<tm1Dunw>/Y	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029003	M	MP:0012098	increased spongiotrophoblast size	Cited1<tm1Dunw>/Y	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029003	M	MP:0011088	neonatal lethality, incomplete penetrance	Cited1<tm1Dunw>/Y	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029003	M	MP:0009674	decreased birth weight	Cited1<tm1Dunw>/Y	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029003	M	MP:0011527	disorganized placental labyrinth	Cited1<tm1Dunw>/Y	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029004	F	MP:0001711	abnormal placenta morphology	Cited1<tm1Dunw>/Cited1<tm1Dunw>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029004	F	MP:0002086	abnormal extraembryonic tissue morphology	Cited1<tm1Dunw>/Cited1<tm1Dunw>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029004	F	MP:0009674	decreased birth weight	Cited1<tm1Dunw>/Cited1<tm1Dunw>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029004	F	MP:0009431	decreased fetal weight	Cited1<tm1Dunw>/Cited1<tm1Dunw>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029004	F	MP:0003231	abnormal placenta vasculature	Cited1<tm1Dunw>/Cited1<tm1Dunw>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029004	F	MP:0011088	neonatal lethality, incomplete penetrance	Cited1<tm1Dunw>/Cited1<tm1Dunw>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029008	F	MP:0011088	neonatal lethality, incomplete penetrance	Cited1<tm1Dunw>/Cited1<+>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029008	F	MP:0003123	paternal imprinting	Cited1<tm1Dunw>/Cited1<+>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029008	F	MP:0001711	abnormal placenta morphology	Cited1<tm1Dunw>/Cited1<+>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029008	F	MP:0008803	abnormal placental labyrinth vasculature morphology	Cited1<tm1Dunw>/Cited1<+>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029008	F	MP:0009431	decreased fetal weight	Cited1<tm1Dunw>/Cited1<+>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029008	F	MP:0002086	abnormal extraembryonic tissue morphology	Cited1<tm1Dunw>/Cited1<+>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029008	F	MP:0009674	decreased birth weight	Cited1<tm1Dunw>/Cited1<+>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029008	F	MP:0003231	abnormal placenta vasculature	Cited1<tm1Dunw>/Cited1<+>	B6.129P2-Cited1<tm1Dunw>	N	14673158
MGI:3029324	M	MP:0001925	male infertility	Kit<Ssm>/Kit<+>	involves: C57BL/10 * Non-inbred	N	MGI:62198
MGI:3029332	F	MP:0001386	abnormal maternal nurturing	Edaradd<cr>/Edaradd<cr>	involves: C57BL/6 * C3H	N	24539712
MGI:3029332	F	MP:0001923	reduced female fertility	Edaradd<cr>/Edaradd<cr>	involves: C57BL/6 * C3H	N	24539712
MGI:3029356	F	MP:0001923	reduced female fertility	Slc6a6<tm1Dhau>/Slc6a6<tm1Dhau>	involves: 129X1/SvJ * C57BL/6J	N	11772953
MGI:3029374	F	MP:0002907	abnormal parturition	Srd5a1<tm1Mahe>/Srd5a1<tm1Mahe>	involves: 129S7/SvEvBrd * C57BL/6J	N	8721983
MGI:3029376	M	MP:0001157	small seminal vesicle	Srd5a2<tm1Mahe>/Srd5a2<tm1Mahe>	involves: 129S/SvEv * C57BL/6J	N	11606430
MGI:3029376	M	MP:0002774	small prostate gland	Srd5a2<tm1Mahe>/Srd5a2<tm1Mahe>	involves: 129S/SvEv * C57BL/6J	N	11606430
MGI:3029376	M	MP:0000664	small prostate gland anterior lobe	Srd5a2<tm1Mahe>/Srd5a2<tm1Mahe>	involves: 129S/SvEv * C57BL/6J	N	11606430
MGI:3029378	M	MP:0001157	small seminal vesicle	Srd5a1<tm1Mahe>/Srd5a1<tm1Mahe>,Srd5a2<tm1Mahe>/Srd5a2<tm1Mahe>	involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6J	N	11606430
MGI:3029378	M	MP:0002774	small prostate gland	Srd5a1<tm1Mahe>/Srd5a1<tm1Mahe>,Srd5a2<tm1Mahe>/Srd5a2<tm1Mahe>	involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6J	N	11606430
MGI:3029378	F	MP:0002907	abnormal parturition	Srd5a1<tm1Mahe>/Srd5a1<tm1Mahe>,Srd5a2<tm1Mahe>/Srd5a2<tm1Mahe>	involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6J	N	11606430
MGI:3029378	M	MP:0000664	small prostate gland anterior lobe	Srd5a1<tm1Mahe>/Srd5a1<tm1Mahe>,Srd5a2<tm1Mahe>/Srd5a2<tm1Mahe>	involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6J	N	11606430
MGI:3029407	M	MP:0003415	priapism	Stam<tm1Sug>/Stam<tm1Sug>	involves: 129S4/SvJae * C57BL/6	N	11340172
MGI:3029407	M	MP:0001925	male infertility	Stam<tm1Sug>/Stam<tm1Sug>	involves: 129S4/SvJae * C57BL/6	N	11340172
MGI:3029427	F	MP:0002169	no abnormal phenotype detected	Abcd1<tm1Kds>/Abcd1<tm1Kds>,Slc27a2<tm1Kds>/Slc27a2<tm1Kds>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J	N	12719378
MGI:3029429	M	MP:0002169	no abnormal phenotype detected	Abcd1<tm1Kds>/Y,Slc27a2<tm1Kds>/Slc27a2<tm1Kds>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J	N	12719378
MGI:3029556	F	MP:0001386	abnormal maternal nurturing	Mprf<LG/J>/Mprf<SM/J>	involves: LG/J * SM/J	N	12454078
MGI:3029634	F	MP:0005389	reproductive system phenotype	Piwil2<tm1Nkn>/Piwil2<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	Y	14736746
MGI:3029634	M	MP:0008261	arrest of male meiosis	Piwil2<tm1Nkn>/Piwil2<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	14736746
MGI:3029634	M	MP:0005159	azoospermia	Piwil2<tm1Nkn>/Piwil2<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	14736746
MGI:3029634	M	MP:0004852	decreased testis weight	Piwil2<tm1Nkn>/Piwil2<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	14736746
MGI:3029634	M	MP:0001925	male infertility	Piwil2<tm1Nkn>/Piwil2<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	14736746
MGI:3029634	M	MP:0014052	increased male germ cell apoptosis	Piwil2<tm1Nkn>/Piwil2<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	N	14736746
MGI:3029670	F	MP:0001923	reduced female fertility	Foxl2<tm1Tre>/Foxl2<+>	involves: 129P2/OlaHsd * Black Swiss * CD-1	N	14736745
MGI:3029674	M	MP:0005389	reproductive system phenotype	Foxl2<tm1Tre>/Foxl2<tm1Tre>	involves: 129P2/OlaHsd * Black Swiss * CD-1	Y	14736745
MGI:3029674	F	MP:0001127	small ovary	Foxl2<tm1Tre>/Foxl2<tm1Tre>	involves: 129P2/OlaHsd * Black Swiss * CD-1	N	14736745
MGI:3029674	F	MP:0001132	absent mature ovarian follicles	Foxl2<tm1Tre>/Foxl2<tm1Tre>	involves: 129P2/OlaHsd * Black Swiss * CD-1	N	14736745
MGI:3029674	M	MP:0031239	increased atretic ovarian follicle number	Foxl2<tm1Tre>/Foxl2<tm1Tre>	involves: 129P2/OlaHsd * Black Swiss * CD-1	N	14736745
MGI:3029674	F	MP:0031382	absent secondary ovarian follicles	Foxl2<tm1Tre>/Foxl2<tm1Tre>	involves: 129P2/OlaHsd * Black Swiss * CD-1	N	14736745
MGI:3029674	F	MP:0001129	impaired ovarian folliculogenesis	Foxl2<tm1Tre>/Foxl2<tm1Tre>	involves: 129P2/OlaHsd * Black Swiss * CD-1	N	14736745
MGI:3029674	M	MP:0031018	decreased granulosa cell proliferation	Foxl2<tm1Tre>/Foxl2<tm1Tre>	involves: 129P2/OlaHsd * Black Swiss * CD-1	N	14736745
MGI:3029674	F	MP:0011122	absent primordial ovarian follicles	Foxl2<tm1Tre>/Foxl2<tm1Tre>	involves: 129P2/OlaHsd * Black Swiss * CD-1	N	14736745
MGI:3029674	F	MP:0001926	female infertility	Foxl2<tm1Tre>/Foxl2<tm1Tre>	involves: 129P2/OlaHsd * Black Swiss * CD-1	N	14736745
MGI:3029674	F	MP:0003357	impaired granulosa cell differentiation	Foxl2<tm1Tre>/Foxl2<tm1Tre>	involves: 129P2/OlaHsd * Black Swiss * CD-1	N	14736745
MGI:3029933	M	MP:0001925	male infertility	Kit<W-ei>/Kit<W-ei>	C57BL-Kit<W-ei>	N	MGI:75732
MGI:3029933	F	MP:0001926	female infertility	Kit<W-ei>/Kit<W-ei>	C57BL-Kit<W-ei>	N	MGI:75732
MGI:3032447	M	MP:0002631	abnormal epididymis morphology	Slc22a5<jvs>/Slc22a5<jvs>	C3.OH-H2<o2> Slc22a5<jvs>	N	10100867
MGI:3032447	M	MP:0001145	abnormal male reproductive system morphology	Slc22a5<jvs>/Slc22a5<jvs>	C3.OH-H2<o2> Slc22a5<jvs>	N	10100867
MGI:3032447	M	MP:0002661	abnormal corpus epididymis morphology	Slc22a5<jvs>/Slc22a5<jvs>	C3.OH-H2<o2> Slc22a5<jvs>	N	10100867
MGI:3032447	M	MP:0004928	increased epididymis weight	Slc22a5<jvs>/Slc22a5<jvs>	C3.OH-H2<o2> Slc22a5<jvs>	N	10100867
MGI:3032500	F	MP:0002075	abnormal coat/hair pigmentation	Stol<1Jrt>/Stol<+>	involves: C3H/HeJ * C57BL/6J	N	MGI:3029973
MGI:3032501	M	MP:0002074	abnormal hair texture	Stol<1Jrt>/Y	involves: C3H/HeJ * C57BL/6J	N	MGI:3029973
MGI:3032501	M	MP:0000416	sparse hair	Stol<1Jrt>/Y	involves: C3H/HeJ * C57BL/6J	N	MGI:3029973
MGI:3032501	M	MP:0005409	darkened coat color	Stol<1Jrt>/Y	involves: C3H/HeJ * C57BL/6J	N	MGI:3029973
MGI:3032501	M	MP:0005382	craniofacial phenotype	Stol<1Jrt>/Y	involves: C3H/HeJ * C57BL/6J	Y	MGI:3029973
MGI:3032501	M	MP:0006236	absent Meibomian glands	Stol<1Jrt>/Y	involves: C3H/HeJ * C57BL/6J	N	MGI:3029973
MGI:3032501	M	MP:0001297	microphthalmia	Stol<1Jrt>/Y	involves: C3H/HeJ * C57BL/6J	N	MGI:3029973
MGI:3032502	F	MP:0005382	craniofacial phenotype	Stol<1Jrt>/Stol<1Jrt>	involves: C3H/HeJ * C57BL/6J	Y	MGI:3029973
MGI:3032502	F	MP:0000416	sparse hair	Stol<1Jrt>/Stol<1Jrt>	involves: C3H/HeJ * C57BL/6J	N	MGI:3029973
MGI:3032502	F	MP:0005409	darkened coat color	Stol<1Jrt>/Stol<1Jrt>	involves: C3H/HeJ * C57BL/6J	N	MGI:3029973
MGI:3032502	F	MP:0002074	abnormal hair texture	Stol<1Jrt>/Stol<1Jrt>	involves: C3H/HeJ * C57BL/6J	N	MGI:3029973
MGI:3032502	F	MP:0001297	microphthalmia	Stol<1Jrt>/Stol<1Jrt>	involves: C3H/HeJ * C57BL/6J	N	MGI:3029973
MGI:3032502	F	MP:0006236	absent Meibomian glands	Stol<1Jrt>/Stol<1Jrt>	involves: C3H/HeJ * C57BL/6J	N	MGI:3029973
MGI:3032586	F	MP:0000947	convulsive seizures	Syn1<tm1Sud>/Syn1<tm1Sud>	involves: 129S7/SvEvBrd	N	7902212
MGI:3032586	F	MP:0002919	enhanced paired-pulse facilitation	Syn1<tm1Sud>/Syn1<tm1Sud>	involves: 129S7/SvEvBrd	N	7902212
MGI:3032587	F	MP:0002916	increased synaptic depression	Syn1<tm1Pggd>/Syn1<tm1Pggd>	involves: 129	N	7568108
MGI:3032587	F	MP:0002912	abnormal excitatory postsynaptic potential	Syn1<tm1Pggd>/Syn1<tm1Pggd>	involves: 129	N	7568108
MGI:3032587	F	MP:0002924	delayed CNS synapse formation	Syn1<tm1Pggd>/Syn1<tm1Pggd>	involves: 129	N	7568107
MGI:3032587	F	MP:0009940	abnormal hippocampus pyramidal cell morphology	Syn1<tm1Pggd>/Syn1<tm1Pggd>	involves: 129	N	7568107
MGI:3032587	F	MP:0004793	abnormal synaptic vesicle clustering	Syn1<tm1Pggd>/Syn1<tm1Pggd>	involves: 129	N	7568108
MGI:3032587	F	MP:0005445	abnormal neurotransmitter secretion	Syn1<tm1Pggd>/Syn1<tm1Pggd>	involves: 129	N	7568108
MGI:3032587	F	MP:0001650	abnormal seizure response to electrical stimulation	Syn1<tm1Pggd>/Syn1<tm1Pggd>	involves: 129	N	7568108
MGI:3032591	F	MP:0031420	decreased superovulation rate	Ptger2<tm1Brey>/Ptger2<tm1Brey>	involves: 129S6/SvEvTac * C57BL/6	N	11319164
MGI:3032591	F	MP:0001923	reduced female fertility	Ptger2<tm1Brey>/Ptger2<tm1Brey>	involves: 129S6/SvEvTac * C57BL/6	N	9930871
MGI:3032602	F	MP:0002922	decreased post-tetanic potentiation	Syn1<tm1Sud>/Syn1<tm1Sud>,Syn2<tm1Sud>/Syn2<tm1Sud>	involves: 129S7/SvEvBrd	N	7777057
MGI:3032602	F	MP:0000947	convulsive seizures	Syn1<tm1Sud>/Syn1<tm1Sud>,Syn2<tm1Sud>/Syn2<tm1Sud>	involves: 129S7/SvEvBrd	N	7777057
MGI:3032602	F	MP:0002916	increased synaptic depression	Syn1<tm1Sud>/Syn1<tm1Sud>,Syn2<tm1Sud>/Syn2<tm1Sud>	involves: 129S7/SvEvBrd	N	7777057
MGI:3032629	F	MP:0001120	abnormal uterus morphology	Actb<tm2(Tag)Arge>/Actb<+>,Tg(Hsp70-1-cre)1Arge/0	involves: 129S1/Sv * C57BL/6J * CBA	N	14661057
MGI:3032629	M	MP:0002997	enlarged seminal vesicle	Actb<tm2(Tag)Arge>/Actb<+>,Tg(Hsp70-1-cre)1Arge/0	involves: 129S1/Sv * C57BL/6J * CBA	N	14661057
MGI:3032665	F	MP:0000628	abnormal mammary gland development	Pgr<tm1Lyd>/Pgr<tm1Lyd>	involves: 129S7/SvEvBrd * C57BL/6	N	12403837
MGI:3032665	F	MP:0001134	absent corpus luteum	Pgr<tm1Lyd>/Pgr<tm1Lyd>	involves: 129S7/SvEvBrd * C57BL/6	N	12403837
MGI:3032665	F	MP:0001926	female infertility	Pgr<tm1Lyd>/Pgr<tm1Lyd>	involves: 129S7/SvEvBrd * C57BL/6	N	12403837
MGI:3032665	F	MP:0001928	abnormal ovulation	Pgr<tm1Lyd>/Pgr<tm1Lyd>	involves: 129S7/SvEvBrd * C57BL/6	N	12403837
MGI:3032665	F	MP:0002566	abnormal sexual interaction	Pgr<tm1Lyd>/Pgr<tm1Lyd>	involves: 129S7/SvEvBrd * C57BL/6	N	12403837
MGI:3032665	F	MP:0001119	abnormal female reproductive system morphology	Pgr<tm1Lyd>/Pgr<tm1Lyd>	involves: 129S7/SvEvBrd * C57BL/6	N	12403837
MGI:3032665	F	MP:0002676	uterus hyperplasia	Pgr<tm1Lyd>/Pgr<tm1Lyd>	involves: 129S7/SvEvBrd * C57BL/6	N	12403837
MGI:3032962	M	MP:0006423	dilated rete testis	Slc9a3<tm1Ges>/Slc9a3<tm1Ges>	Not Specified	N	11698654
MGI:3032962	M	MP:0001925	male infertility	Slc9a3<tm1Ges>/Slc9a3<tm1Ges>	Not Specified	N	11698654
MGI:3032962	M	MP:0009140	dilated efferent ductule of testis	Slc9a3<tm1Ges>/Slc9a3<tm1Ges>	Not Specified	N	11698654
MGI:3033191	F	MP:0013716	hypolactation	Slc30a4<lm>/Slc30a4<lm>	C57BL/6J-Slc30a4<lm>	N	619449
MGI:3033191	F	MP:0020894	abnormal milk zinc level	Slc30a4<lm>/Slc30a4<lm>	C57BL/6J-Slc30a4<lm>	N	619449
MGI:3033191	F	MP:0004047	abnormal milk composition	Slc30a4<lm>/Slc30a4<lm>	C57BL/6J-Slc30a4<lm>	N	MGI:78287
MGI:3033191	F	MP:0020894	abnormal milk zinc level	Slc30a4<lm>/Slc30a4<lm>	C57BL/6J-Slc30a4<lm>	N	6512240
MGI:3033191	F	MP:0006270	abnormal mammary gland growth during lactation	Slc30a4<lm>/Slc30a4<lm>	C57BL/6J-Slc30a4<lm>	N	619449
MGI:3033364	M	MP:0008261	arrest of male meiosis	Slc19a2<tm1Gelb>/Slc19a2<tm1Gelb>	involves: 129X1/SvJ	N	14738878
MGI:3033364	M	MP:0001925	male infertility	Slc19a2<tm1Gelb>/Slc19a2<tm1Gelb>	involves: 129X1/SvJ	N	14738878
MGI:3033364	M	MP:0005159	azoospermia	Slc19a2<tm1Gelb>/Slc19a2<tm1Gelb>	involves: 129X1/SvJ	N	14738878
MGI:3033364	M	MP:0004852	decreased testis weight	Slc19a2<tm1Gelb>/Slc19a2<tm1Gelb>	involves: 129X1/SvJ	N	14738878
MGI:3033364	M	MP:0006380	abnormal spermatid morphology	Slc19a2<tm1Gelb>/Slc19a2<tm1Gelb>	involves: 129X1/SvJ	N	14738878
MGI:3033364	M	MP:0001156	abnormal spermatogenesis	Slc19a2<tm1Gelb>/Slc19a2<tm1Gelb>	involves: 129X1/SvJ	N	14738878
MGI:3033449	M	MP:0001925	male infertility	Kit<W-1Bao>/Kit<+>	C57BL/6J-Kit<W-1Bao>	N	MGI:3029325
MGI:3033449	M	MP:0001922	reduced male fertility	Kit<W-1Bao>/Kit<+>	C57BL/6J-Kit<W-1Bao>	N	MGI:3029325
MGI:3033494	F	MP:0002023	increased B cell derived lymphoma incidence	Suv39h1<tm1Jnw>/Suv39h1<+>	involves: 129 * C57BL/6J	N	11701123
MGI:3033495	F	MP:0002023	increased B cell derived lymphoma incidence	Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>	involves: 129 * C57BL/6J	N	11701123
MGI:3033496	F	MP:0001698	decreased embryo size	Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>	involves: 129 * C57BL/6J	N	11701123
MGI:3033496	M	MP:0008261	arrest of male meiosis	Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>	involves: 129 * C57BL/6J	N	11701123
MGI:3033496	F	MP:0001924	infertility	Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>	involves: 129 * C57BL/6J	N	11701123
MGI:3033496	F	MP:0011101	prenatal lethality, incomplete penetrance	Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>	involves: 129 * C57BL/6J	N	11701123
MGI:3033496	F	MP:0001116	small gonad	Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>	involves: 129 * C57BL/6J	N	11701123
MGI:3033496	F	MP:0001732	postnatal growth retardation	Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>	involves: 129 * C57BL/6J	N	11701123
MGI:3033497	F	MP:0002023	increased B cell derived lymphoma incidence	Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<+>	involves: 129 * C57BL/6J	N	11701123
MGI:3033498	F	MP:0002023	increased B cell derived lymphoma incidence	Suv39h1<tm1Jnw>/Suv39h1<+>,Suv39h2<tm1Jnw>/Suv39h2<+>	involves: 129 * C57BL/6J	N	11701123
MGI:3033499	F	MP:0002023	increased B cell derived lymphoma incidence	Suv39h1<tm1Jnw>/Suv39h1<+>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>	involves: 129 * C57BL/6J	N	11701123
MGI:3033578	F	MP:0006278	aortic aneurysm	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	15680392
MGI:3033578	F	MP:0009021	absent estrus	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	10952938
MGI:3033578	F	MP:0006278	aortic aneurysm	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	15364874
MGI:3033578	F	MP:0009018	short estrus	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	10952938
MGI:3033578	F	MP:0009009	absent estrous cycle	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	10952938
MGI:3033578	F	MP:0005185	decreased circulating progesterone level	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	10952938
MGI:3033578	F	MP:0002411	decreased susceptibility to bacterial infection	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	15618213
MGI:3033578	F	MP:0005378	growth/size/body region phenotype	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	Y	9160717
MGI:3033578	F	MP:0009016	abnormal estrus	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	10952938
MGI:3033578	F	MP:0001923	reduced female fertility	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	11732988
MGI:3033578	F	MP:0002006	neoplasm	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	Y	8957071
MGI:3033578	F	MP:0000343	abnormal response to cardiac infarction	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	15598866
MGI:3033578	F	MP:0005397	hematopoietic system phenotype	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	Y	16107690
MGI:3033578	F	MP:0004904	increased uterus weight	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	15084483
MGI:3033578	F	MP:0003819	increased left ventricle diastolic pressure	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	10652195
MGI:3033578	F	MP:0000333	decreased bone marrow cell number	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	16107690
MGI:3033578	F	MP:0003572	abnormal uterus development	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	15084483
MGI:3033578	F	MP:0004904	increased uterus weight	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	10952938
MGI:3033578	F	MP:0005182	increased circulating estradiol level	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	10952938
MGI:3033578	F	MP:0013400	abnormal endometrial gland development	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	15084483
MGI:3033578	F	MP:0009014	prolonged proestrus	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	10952938
MGI:3033578	F	MP:0005389	reproductive system phenotype	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	Y	9160717
MGI:3033578	F	MP:0001935	decreased litter size	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	11732988
MGI:3033580	M	MP:0006278	aortic aneurysm	Timp1<tm1Pds>/Y	involves: 129S4/SvJae	N	15364874
MGI:3033580	M	MP:0000343	abnormal response to cardiac infarction	Timp1<tm1Pds>/Y	involves: 129S4/SvJae	N	15598866
MGI:3033580	M	MP:0006278	aortic aneurysm	Timp1<tm1Pds>/Y	involves: 129S4/SvJae	N	15680392
MGI:3033580	M	MP:0003819	increased left ventricle diastolic pressure	Timp1<tm1Pds>/Y	involves: 129S4/SvJae	N	10652195
MGI:3033580	M	MP:0004851	increased testis weight	Timp1<tm1Pds>/Y	involves: 129S4/SvJae	N	9687309
MGI:3033580	M	MP:0005378	growth/size/body region phenotype	Timp1<tm1Pds>/Y	involves: 129S4/SvJae	Y	9687309
MGI:3033580	M	MP:0002781	increased circulating testosterone level	Timp1<tm1Pds>/Y	involves: 129S4/SvJae	N	9687309
MGI:3033595	M	MP:0002687	oligozoospermia	Tarbp2<tm1Reb>/Tarbp2<tm1Reb>	Not Specified	N	10369260
MGI:3033595	M	MP:0001932	abnormal spermiogenesis	Tarbp2<tm1Reb>/Tarbp2<tm1Reb>	Not Specified	N	10369260
MGI:3033595	M	MP:0001925	male infertility	Tarbp2<tm1Reb>/Tarbp2<tm1Reb>	Not Specified	N	10369260
MGI:3033643	M	MP:0001925	male infertility	Slc4a2<tm1Jmed>/Slc4a2<tm1Jmed>	involves: 129P2/OlaHsd * FVB	N	14673081
MGI:3033643	M	MP:0001940	testis hypoplasia	Slc4a2<tm1Jmed>/Slc4a2<tm1Jmed>	involves: 129P2/OlaHsd * FVB	N	14673081
MGI:3033643	M	MP:0002660	abnormal caput epididymis morphology	Slc4a2<tm1Jmed>/Slc4a2<tm1Jmed>	involves: 129P2/OlaHsd * FVB	N	14673081
MGI:3033643	M	MP:0002662	abnormal cauda epididymis morphology	Slc4a2<tm1Jmed>/Slc4a2<tm1Jmed>	involves: 129P2/OlaHsd * FVB	N	14673081
MGI:3033643	M	MP:0001932	abnormal spermiogenesis	Slc4a2<tm1Jmed>/Slc4a2<tm1Jmed>	involves: 129P2/OlaHsd * FVB	N	14673081
MGI:3033643	M	MP:0001147	small testis	Slc4a2<tm1Jmed>/Slc4a2<tm1Jmed>	involves: 129P2/OlaHsd * FVB	N	14673081
MGI:3033643	M	MP:0005159	azoospermia	Slc4a2<tm1Jmed>/Slc4a2<tm1Jmed>	involves: 129P2/OlaHsd * FVB	N	14673081
MGI:3033643	M	MP:0005250	decreased Sertoli cell number	Slc4a2<tm1Jmed>/Slc4a2<tm1Jmed>	involves: 129P2/OlaHsd * FVB	N	14673081
MGI:3033643	M	MP:0002661	abnormal corpus epididymis morphology	Slc4a2<tm1Jmed>/Slc4a2<tm1Jmed>	involves: 129P2/OlaHsd * FVB	N	14673081
MGI:3033643	M	MP:0002631	abnormal epididymis morphology	Slc4a2<tm1Jmed>/Slc4a2<tm1Jmed>	involves: 129P2/OlaHsd * FVB	N	14673081
MGI:3033752	F	MP:0000745	tremors	Plp1<jp-rsh>/Plp1<jp-rsh>	involves: 101 * C3H	N	MGI:62318
MGI:3033752	F	MP:0005386	behavior/neurological phenotype	Plp1<jp-rsh>/Plp1<jp-rsh>	involves: 101 * C3H	Y	MGI:62318
MGI:3033752	F	MP:0000921	demyelination	Plp1<jp-rsh>/Plp1<jp-rsh>	involves: 101 * C3H	N	MGI:62318
MGI:3033752	F	MP:0002182	abnormal astrocyte morphology	Plp1<jp-rsh>/Plp1<jp-rsh>	involves: 101 * C3H	N	1694232
MGI:3033752	F	MP:0000921	demyelination	Plp1<jp-rsh>/Plp1<jp-rsh>	involves: 101 * C3H	N	1694232
MGI:3033752	F	MP:0005389	reproductive system phenotype	Plp1<jp-rsh>/Plp1<jp-rsh>	involves: 101 * C3H	Y	MGI:62318
MGI:3033752	F	MP:0005378	growth/size/body region phenotype	Plp1<jp-rsh>/Plp1<jp-rsh>	involves: 101 * C3H	Y	MGI:62318
MGI:3033752	F	MP:0000745	tremors	Plp1<jp-rsh>/Plp1<jp-rsh>	involves: 101 * C3H	N	1694232
MGI:3033752	F	MP:0010160	increased oligodendrocyte number	Plp1<jp-rsh>/Plp1<jp-rsh>	involves: 101 * C3H	N	1694232
MGI:3033753	M	MP:0000913	abnormal brain development	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	12645075
MGI:3033753	M	MP:0004768	abnormal axonal transport	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	20091761
MGI:3033753	M	MP:0003354	astrocytosis	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	12645075
MGI:3033753	M	MP:0005386	behavior/neurological phenotype	Plp1<jp-rsh>/Y	involves: 101 * C3H	Y	MGI:62318
MGI:3033753	M	MP:0013438	dysmyelination	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	20091761
MGI:3033753	M	MP:0000921	demyelination	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	12645075
MGI:3033753	M	MP:0003634	abnormal glial cell morphology	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	12645075
MGI:3033753	M	MP:0010160	increased oligodendrocyte number	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	1694232
MGI:3033753	M	MP:0000921	demyelination	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	1694232
MGI:3033753	M	MP:0000745	tremors	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	MGI:62318
MGI:3033753	M	MP:0000745	tremors	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	1694232
MGI:3033753	M	MP:0000745	tremors	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	12645075
MGI:3033753	M	MP:0005378	growth/size/body region phenotype	Plp1<jp-rsh>/Y	involves: 101 * C3H	Y	MGI:62318
MGI:3033753	M	MP:0002182	abnormal astrocyte morphology	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	1694232
MGI:3033753	M	MP:0000921	demyelination	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	MGI:62318
MGI:3033753	M	MP:0001405	impaired coordination	Plp1<jp-rsh>/Y	involves: 101 * C3H	N	12645075
MGI:3033753	M	MP:0005389	reproductive system phenotype	Plp1<jp-rsh>/Y	involves: 101 * C3H	Y	MGI:62318
MGI:3033756	M	MP:0014071	increased cardiac muscle glycogen level	Gaa<tm1Rabn>/Gaa<tm1Rabn>	involves: 129X1/SvJ * C57BL/6	N	27358407
MGI:3033756	M	MP:0010401	increased skeletal muscle glycogen level	Gaa<tm1Rabn>/Gaa<tm1Rabn>	involves: 129X1/SvJ * C57BL/6	N	27358407
MGI:3033756	M	MP:0010400	increased liver glycogen level	Gaa<tm1Rabn>/Gaa<tm1Rabn>	involves: 129X1/SvJ * C57BL/6	N	27358407
MGI:3033770	M	MP:0001402	decreased locomotor activity	Plp1<jp-rsh>/Y	involves: C57BL/6NCrl	N	12645075
MGI:3033770	M	MP:0002064	seizures	Plp1<jp-rsh>/Y	involves: C57BL/6NCrl	N	12645075
MGI:3033770	M	MP:0001262	decreased body weight	Plp1<jp-rsh>/Y	involves: C57BL/6NCrl	N	12645075
MGI:3033770	M	MP:0003634	abnormal glial cell morphology	Plp1<jp-rsh>/Y	involves: C57BL/6NCrl	N	12645075
MGI:3033770	M	MP:0000921	demyelination	Plp1<jp-rsh>/Y	involves: C57BL/6NCrl	N	12645075
MGI:3033770	M	MP:0002083	premature death	Plp1<jp-rsh>/Y	involves: C57BL/6NCrl	N	12645075
MGI:3033770	M	MP:0003354	astrocytosis	Plp1<jp-rsh>/Y	involves: C57BL/6NCrl	N	12645075
MGI:3033770	M	MP:0000745	tremors	Plp1<jp-rsh>/Y	involves: C57BL/6NCrl	N	12645075
MGI:3033770	M	MP:0000913	abnormal brain development	Plp1<jp-rsh>/Y	involves: C57BL/6NCrl	N	12645075
MGI:3033770	M	MP:0001405	impaired coordination	Plp1<jp-rsh>/Y	involves: C57BL/6NCrl	N	12645075
MGI:3033848	M	MP:0003642	absent seminal vesicle	Rara<tm1Ipc>/Rara<tm1Ipc>,Rarg<tm1Ipc>/Rarg<tm1Ipc>	involves: 129S2/SvPas	N	7607068
MGI:3033848	F	MP:0009072	absent cranial vagina	Rara<tm1Ipc>/Rara<tm1Ipc>,Rarg<tm1Ipc>/Rarg<tm1Ipc>	involves: 129S2/SvPas	N	7607068
MGI:3033848	F	MP:0003558	absent uterus	Rara<tm1Ipc>/Rara<tm1Ipc>,Rarg<tm1Ipc>/Rarg<tm1Ipc>	involves: 129S2/SvPas	N	7607068
MGI:3033848	M	MP:0003557	absent vas deferens	Rara<tm1Ipc>/Rara<tm1Ipc>,Rarg<tm1Ipc>/Rarg<tm1Ipc>	involves: 129S2/SvPas	N	7607068
MGI:3033848	F	MP:0001120	abnormal uterus morphology	Rara<tm1Ipc>/Rara<tm1Ipc>,Rarg<tm1Ipc>/Rarg<tm1Ipc>	involves: 129S2/SvPas	N	7607068
MGI:3033862	F	MP:0003558	absent uterus	Rara<tm2Ipc>/Rara<tm2Ipc>,Rarb<tm1Ipc>/Rarb<tm1Ipc>	involves: 129S2/SvPas	N	7607068
MGI:3033862	F	MP:0001119	abnormal female reproductive system morphology	Rara<tm2Ipc>/Rara<tm2Ipc>,Rarb<tm1Ipc>/Rarb<tm1Ipc>	involves: 129S2/SvPas	N	7607068
MGI:3033862	F	MP:0009072	absent cranial vagina	Rara<tm2Ipc>/Rara<tm2Ipc>,Rarb<tm1Ipc>/Rarb<tm1Ipc>	involves: 129S2/SvPas	N	7607068
MGI:3033884	F	MP:0005577	uterus prolapse	Loxl1<tm1Tili>/Loxl1<tm1Tili>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	14745449
MGI:3033884	F	MP:0001136	dilated uterine cervix	Loxl1<tm1Tili>/Loxl1<tm1Tili>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	14745449
MGI:3033964	F	MP:0001926	female infertility	Hsf1<tm1Miv>/Hsf1<tm1Miv>	involves: 129S2/SvPas * C57BL/6	N	12112007
MGI:3033965	M	MP:0001925	male infertility	Hsf1<tm1Miv>/Hsf1<tm1Miv>,Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	14994269
MGI:3033965	M	MP:0008261	arrest of male meiosis	Hsf1<tm1Miv>/Hsf1<tm1Miv>,Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	14994269
MGI:3033965	M	MP:0001146	abnormal testis morphology	Hsf1<tm1Miv>/Hsf1<tm1Miv>,Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	14994269
MGI:3033965	F	MP:0001926	female infertility	Hsf1<tm1Miv>/Hsf1<tm1Miv>,Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	14994269
MGI:3033965	M	MP:0001147	small testis	Hsf1<tm1Miv>/Hsf1<tm1Miv>,Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	14994269
MGI:3033965	M	MP:0020550	multinucleated giant male germ cells	Hsf1<tm1Miv>/Hsf1<tm1Miv>,Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	14994269
MGI:3033965	M	MP:0002216	abnormal seminiferous tubule morphology	Hsf1<tm1Miv>/Hsf1<tm1Miv>,Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	14994269
MGI:3033965	M	MP:0005159	azoospermia	Hsf1<tm1Miv>/Hsf1<tm1Miv>,Hsf2<tm1Miv>/Hsf2<tm1Miv>	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	14994269
MGI:3034015	M	MP:0001380	reduced male mating frequency	Strbp<Gt(pGT1.8geo)8Pgr>/Strbp<Gt(pGT1.8geo)8Pgr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11336498
MGI:3034015	M	MP:0004852	decreased testis weight	Strbp<Gt(pGT1.8geo)8Pgr>/Strbp<Gt(pGT1.8geo)8Pgr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11336498
MGI:3034015	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Strbp<Gt(pGT1.8geo)8Pgr>/Strbp<Gt(pGT1.8geo)8Pgr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11336498
MGI:3034015	M	MP:0001922	reduced male fertility	Strbp<Gt(pGT1.8geo)8Pgr>/Strbp<Gt(pGT1.8geo)8Pgr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11336498
MGI:3034015	M	MP:0001156	abnormal spermatogenesis	Strbp<Gt(pGT1.8geo)8Pgr>/Strbp<Gt(pGT1.8geo)8Pgr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11336498
MGI:3034015	M	MP:0002687	oligozoospermia	Strbp<Gt(pGT1.8geo)8Pgr>/Strbp<Gt(pGT1.8geo)8Pgr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11336498
MGI:3034015	M	MP:0002675	asthenozoospermia	Strbp<Gt(pGT1.8geo)8Pgr>/Strbp<Gt(pGT1.8geo)8Pgr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11336498
MGI:3034040	F	MP:0002169	no abnormal phenotype detected	Syp<tm1Leu>/Syp<tm1Leu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	8581936
MGI:3034077	F	MP:0002169	no abnormal phenotype detected	Xiap<tm1Thsn>/Xiap<tm1Thsn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11313486
MGI:3035817	F	MP:0001728	failure of embryo implantation	Smarcb1<Gt(OST32815)Lex>/Smarcb1<Gt(OST32815)Lex>	either: (involves: 129 * 129S5/SvEvBrd) or (involves: 129S5/SvEvBrd * C57BL/6)	N	11313485
MGI:3035910	F	MP:0001728	failure of embryo implantation	Smarcb1<tm1Mya>/Smarcb1<tm1Mya>	involves: 129S2/SvPas * C57BL/6	N	11263494
MGI:3036099	M	MP:0001875	testis inflammation	Kif1c<Orch3-BALB/cByJ>/Kif1c<Orch3-BALB/cByJ>	involves: BALB/cByJ * DBA/2	N	7777570
MGI:3036100	M	MP:0001875	testis inflammation	Orch4<BALB/cByJ>/Orch4<BALB/cByJ>	involves: BALB/cByJ * DBA/2	N	7777570
MGI:3036101	M	MP:0001875	testis inflammation	Orch5<BALB/cByJ>/Orch5<BALB/cByJ>	involves: BALB/cByJ * DBA/2	N	7777570
MGI:3036125	M	MP:0014052	increased male germ cell apoptosis	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	14745012
MGI:3036125	M	MP:0008261	arrest of male meiosis	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	14745012
MGI:3036125	M	MP:0006379	abnormal spermatocyte morphology	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	14745012
MGI:3036125	M	MP:0001155	arrest of spermatogenesis	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	14745012
MGI:3036125	M	MP:0004852	decreased testis weight	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	15919750
MGI:3036125	M	MP:0005378	growth/size/body region phenotype	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	Y	14745012
MGI:3036125	M	MP:0002786	abnormal Leydig cell morphology	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	15919750
MGI:3036125	M	MP:0001147	small testis	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	14745012
MGI:3036125	M	MP:0005536	decreased Leydig cell number	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	15919750
MGI:3036125	M	MP:0004852	decreased testis weight	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	14745012
MGI:3036125	M	MP:0001153	small seminiferous tubules	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	14745012
MGI:3036125	M	MP:0004929	decreased epididymis weight	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	14745012
MGI:3036125	M	MP:0005159	azoospermia	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	14745012
MGI:3036125	M	MP:0006380	abnormal spermatid morphology	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	14745012
MGI:3036125	M	MP:0001750	increased circulating follicle stimulating hormone level	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	14745012
MGI:3036125	M	MP:0004901	decreased male germ cell number	Ar<tm1Verh>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	14745012
MGI:3036135	F	MP:0003699	abnormal female reproductive system physiology	Ifng<tm1Yiw>/Ifng<tm1Yiw>	involves: 129X1/SvJ * C57BL/6	N	10639149
MGI:3036137	M	MP:0005389	reproductive system phenotype	Ar<tm1Verh>/Y	involves: 129S1/Sv * 129X1/SvJ	Y	14745012
MGI:3036352	M	MP:0010957	abnormal aerobic respiration	Slc25a4<tm2Dwa>/Slc25a4<tm2Dwa>,Slc25a5<tm1Dwa>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/?	involves: 129S4/SvJae	N	14749836
MGI:3036442	F	MP:0002169	no abnormal phenotype detected	Rhox9<tm1Dean>/Rhox9<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11689708
MGI:3036449	F	MP:0001385	pup cannibalization	Foxa2<tm1Khk>/Foxa2<tm1Khk>,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0	involves: 129 * 129P2/OlaHsd * C57BL/6	N	15452354
MGI:3036548	M	MP:0001146	abnormal testis morphology	Skp2<tm1Kin>/Skp2<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	N	10790373
MGI:3036713	F	MP:0001386	abnormal maternal nurturing	Whrn<wi>/Whrn<wi>	involves: C57BL/6J * STOCK a Tyrp1<b> Myo5a<d> Oca2<p> Ednrb<s>	N	14098314
MGI:3036713	M	MP:0004910	decreased seminal vesicle weight	Whrn<wi>/Whrn<wi>	involves: C57BL/6J * STOCK a Tyrp1<b> Myo5a<d> Oca2<p> Ednrb<s>	N	5538400
MGI:3036713	F	MP:0004905	decreased uterus weight	Whrn<wi>/Whrn<wi>	involves: C57BL/6J * STOCK a Tyrp1<b> Myo5a<d> Oca2<p> Ednrb<s>	N	6034501
MGI:3036850	F	MP:0002169	no abnormal phenotype detected	Smpx<tm1.1Rph>/Smpx<tm1.1Rph>	involves: 129S1/Sv * C57BL/6	N	11381084
MGI:3036866	F	MP:0013351	abnormal Rathke's pouch development	Sox3<tm1Rlb>/Sox3<tm1Rlb>	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036866	F	MP:0013342	bifurcated Rathke's pouch	Sox3<tm1Rlb>/Sox3<tm1Rlb>	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036866	F	MP:0000780	abnormal corpus callosum morphology	Sox3<tm1Rlb>/Sox3<tm1Rlb>	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036866	F	MP:0002199	abnormal brain commissure morphology	Sox3<tm1Rlb>/Sox3<tm1Rlb>	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036866	F	MP:0001127	small ovary	Sox3<tm1Rlb>/Sox3<tm1Rlb>	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036866	F	MP:0000830	abnormal diencephalon morphology	Sox3<tm1Rlb>/Sox3<tm1Rlb>	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036866	F	MP:0008221	abnormal hippocampal commissure morphology	Sox3<tm1Rlb>/Sox3<tm1Rlb>	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036866	F	MP:0002082	postnatal lethality	Sox3<tm1Rlb>/Sox3<tm1Rlb>	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036866	F	MP:0031239	increased atretic ovarian follicle number	Sox3<tm1Rlb>/Sox3<tm1Rlb>	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036866	F	MP:0000633	abnormal pituitary gland morphology	Sox3<tm1Rlb>/Sox3<tm1Rlb>	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036866	F	MP:0000826	abnormal third ventricle morphology	Sox3<tm1Rlb>/Sox3<tm1Rlb>	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036866	F	MP:0000837	abnormal hypothalamus morphology	Sox3<tm1Rlb>/Sox3<tm1Rlb>	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036866	F	MP:0005389	reproductive system phenotype	Sox3<tm1Rlb>/Sox3<tm1Rlb>	involves: 129S7/SvEvBrd * MF1	Y	14981518
MGI:3036867	F	MP:0000428	abnormal craniofacial morphology	Sox3<tm1Rlb>/Sox3<+>	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0011086	postnatal lethality, incomplete penetrance	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0013342	bifurcated Rathke's pouch	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0000826	abnormal third ventricle morphology	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0008221	abnormal hippocampal commissure morphology	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0005136	decreased growth hormone level	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0000830	abnormal diencephalon morphology	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0005130	decreased follicle stimulating hormone level	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0000780	abnormal corpus callosum morphology	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0000428	abnormal craniofacial morphology	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0002199	abnormal brain commissure morphology	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0000837	abnormal hypothalamus morphology	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0013351	abnormal Rathke's pouch development	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0005134	decreased thyroid-stimulating hormone level	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0000633	abnormal pituitary gland morphology	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0001146	abnormal testis morphology	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036868	M	MP:0001732	postnatal growth retardation	Sox3<tm1Rlb>/Y	involves: 129S7/SvEvBrd * MF1	N	14981518
MGI:3036915	F	MP:0005027	increased susceptibility to parasitic infection	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6)	N	11404475
MGI:3036915	F	MP:0020913	increased susceptibility to Riboviria infection	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6)	N	11404475
MGI:3036915	F	MP:0002433	abnormal T-helper 1 cell morphology	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6)	N	11404475
MGI:3036915	F	MP:0005348	increased T cell proliferation	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6)	N	11404475
MGI:3036915	F	MP:0002492	decreased IgE level	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6)	N	11404475
MGI:3036915	F	MP:0002434	abnormal T-helper 2 cell morphology	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6)	N	11404475
MGI:3036915	F	MP:0000717	abnormal lymphocyte cell number	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6)	N	11404475
MGI:3036915	F	MP:0002406	increased susceptibility to infection	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6)	N	11404475
MGI:3037127	M	MP:0002286	cryptorchism	Scg5<tm1Led>/Scg5<tm1Led>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * FVB) or (involves: 129S6/SvEvTac * C57BL/6)	N	12021197
MGI:3037539	M	MP:0001922	reduced male fertility	Serpine2<tm1Dmn>/Serpine2<tm1Dmn>	involves: 129P2/OlaHsd * C57BL/6	N	11248026
MGI:3037539	M	MP:0031435	abnormal copulatory plug biosynthesis	Serpine2<tm1Dmn>/Serpine2<tm1Dmn>	involves: 129P2/OlaHsd * C57BL/6	N	11248026
MGI:3037539	M	MP:0013899	abnormal seminal vesicle epithelium morphology	Serpine2<tm1Dmn>/Serpine2<tm1Dmn>	involves: 129P2/OlaHsd * C57BL/6	N	11248026
MGI:3037539	M	MP:0005389	reproductive system phenotype	Serpine2<tm1Dmn>/Serpine2<tm1Dmn>	involves: 129P2/OlaHsd * C57BL/6	Y	11248026
MGI:3037539	M	MP:0013903	abnormal seminal vesicle fluid composition	Serpine2<tm1Dmn>/Serpine2<tm1Dmn>	involves: 129P2/OlaHsd * C57BL/6	N	11248026
MGI:3037539	M	MP:0013320	dilated seminal vesicle	Serpine2<tm1Dmn>/Serpine2<tm1Dmn>	involves: 129P2/OlaHsd * C57BL/6	N	11248026
MGI:3037539	M	MP:0003607	abnormal prostate gland physiology	Serpine2<tm1Dmn>/Serpine2<tm1Dmn>	involves: 129P2/OlaHsd * C57BL/6	N	11248026
MGI:3037539	M	MP:0002059	abnormal seminal vesicle morphology	Serpine2<tm1Dmn>/Serpine2<tm1Dmn>	involves: 129P2/OlaHsd * C57BL/6	N	11248026
MGI:3037638	M	MP:0003167	abnormal scala tympani morphology	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0014322	short hindlimb	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0002116	abnormal craniofacial bone morphology	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0000063	decreased bone mineral density	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0005377	hearing/vestibular/ear phenotype	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	Y	15029877
MGI:3037638	M	MP:0005353	abnormal patella morphology	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0002765	short fibula	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0006397	disorganized long bone epiphyseal plate	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0002764	short tibia	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0000592	short tail	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0001262	decreased body weight	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0005628	decreased circulating potassium level	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0008151	increased diameter of long bones	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0000195	decreased circulating calcium level	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0003109	short femur	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0004686	decreased length of long bones	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037638	M	MP:0005352	small cranium	Phex<Hyp-2J>/Y	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037641	F	MP:0000592	short tail	Phex<Hyp-2J>/Phex<+>	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037641	F	MP:0014322	short hindlimb	Phex<Hyp-2J>/Phex<+>	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037641	F	MP:0002089	abnormal postnatal growth/weight/body size	Phex<Hyp-2J>/Phex<+>	C57BL/6-Phex<Hyp-2J>/J	N	15029877
MGI:3037642	M	MP:0011967	increased or absent threshold for auditory brainstem response	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	18289812
MGI:3037642	M	MP:0005628	decreased circulating potassium level	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0001732	postnatal growth retardation	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0000097	short maxilla	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0002765	short fibula	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0003109	short femur	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0002764	short tibia	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0011967	increased or absent threshold for auditory brainstem response	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0000195	decreased circulating calcium level	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0001262	decreased body weight	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0002857	cochlear ganglion degeneration	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	18289812
MGI:3037642	M	MP:0002857	cochlear ganglion degeneration	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0001850	increased susceptibility to otitis media	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	18289812
MGI:3037642	M	MP:0000039	abnormal otic capsule morphology	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	18289812
MGI:3037642	M	MP:0006397	disorganized long bone epiphyseal plate	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0000031	abnormal cochlea morphology	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0001406	abnormal gait	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	18289812
MGI:3037642	M	MP:0010025	decreased total body fat amount	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0000063	decreased bone mineral density	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0008151	increased diameter of long bones	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0005272	abnormal temporal bone morphology	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0001849	ear inflammation	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	18289812
MGI:3037642	M	MP:0003167	abnormal scala tympani morphology	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0004686	decreased length of long bones	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0002116	abnormal craniofacial bone morphology	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0000592	short tail	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0005352	small cranium	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0004699	unilateral deafness	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	18289812
MGI:3037642	M	MP:0005353	abnormal patella morphology	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0001394	circling	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0001410	head bobbing	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	18289812
MGI:3037642	M	MP:0002115	abnormal limb bone morphology	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0006089	abnormal vestibular saccule morphology	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	18289812
MGI:3037642	M	MP:0006025	distended Reissner membrane	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	18289812
MGI:3037642	M	MP:0005377	hearing/vestibular/ear phenotype	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	Y	18289812
MGI:3037642	M	MP:0014322	short hindlimb	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0000043	organ of Corti degeneration	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	15029877
MGI:3037642	M	MP:0006325	impaired hearing	Phex<Hyp-Duk>/Y	involves: BALB/cAnBomUrd	N	18289812
MGI:3037643	F	MP:0000592	short tail	Phex<Hyp-Duk>/Phex<+>	involves: BALB/cAnBomUrd	N	15029877
MGI:3037643	F	MP:0001394	circling	Phex<Hyp-Duk>/Phex<+>	involves: BALB/cAnBomUrd	N	15029877
MGI:3037643	F	MP:0014322	short hindlimb	Phex<Hyp-Duk>/Phex<+>	involves: BALB/cAnBomUrd	N	15029877
MGI:3037643	F	MP:0001732	postnatal growth retardation	Phex<Hyp-Duk>/Phex<+>	involves: BALB/cAnBomUrd	N	15029877
MGI:3037661	M	MP:0000195	decreased circulating calcium level	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0008151	increased diameter of long bones	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0002765	short fibula	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0000063	decreased bone mineral density	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0001262	decreased body weight	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0006397	disorganized long bone epiphyseal plate	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0010025	decreased total body fat amount	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0002115	abnormal limb bone morphology	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0011967	increased or absent threshold for auditory brainstem response	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0014322	short hindlimb	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0002764	short tibia	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0005353	abnormal patella morphology	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0005628	decreased circulating potassium level	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0000592	short tail	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0003109	short femur	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037661	M	MP:0004686	decreased length of long bones	Gy/Y	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037666	F	MP:0000592	short tail	Gy/Gy<+>	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037666	F	MP:0014322	short hindlimb	Gy/Gy<+>	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037666	F	MP:0002089	abnormal postnatal growth/weight/body size	Gy/Gy<+>	involves: C3H/Sn * C57BL/6Ei	N	15029877
MGI:3037885	M	MP:0001925	male infertility	Serpina5<tm1Gei>/Serpina5<tm1Gei>	involves: 129/Sv * Swiss	N	11120760
MGI:3037885	M	MP:0002216	abnormal seminiferous tubule morphology	Serpina5<tm1Gei>/Serpina5<tm1Gei>	involves: 129/Sv * Swiss	N	11120760
MGI:3037885	M	MP:0001145	abnormal male reproductive system morphology	Serpina5<tm1Gei>/Serpina5<tm1Gei>	involves: 129/Sv * Swiss	N	11120760
MGI:3037885	M	MP:0005578	teratozoospermia	Serpina5<tm1Gei>/Serpina5<tm1Gei>	involves: 129/Sv * Swiss	N	11120760
MGI:3037885	M	MP:0002784	abnormal Sertoli cell morphology	Serpina5<tm1Gei>/Serpina5<tm1Gei>	involves: 129/Sv * Swiss	N	11120760
MGI:3037885	M	MP:0004933	abnormal epididymis epithelium morphology	Serpina5<tm1Gei>/Serpina5<tm1Gei>	involves: 129/Sv * Swiss	N	11120760
MGI:3037885	M	MP:0002675	asthenozoospermia	Serpina5<tm1Gei>/Serpina5<tm1Gei>	involves: 129/Sv * Swiss	N	11120760
MGI:3037930	M	MP:0031356	abnormal outer dense fiber morphology	Tnp2<tm1Mzh>/Tnp2<tm1Mzh>	involves: 129S/SvEv * 129S7/SvEvBrd	N	11585907
MGI:3037930	M	MP:0009838	abnormal sperm axoneme morphology	Tnp2<tm1Mzh>/Tnp2<tm1Mzh>	involves: 129S/SvEv * 129S7/SvEvBrd	N	11585907
MGI:3037930	M	MP:0002675	asthenozoospermia	Tnp2<tm1Mzh>/Tnp2<tm1Mzh>	involves: 129S/SvEv * 129S7/SvEvBrd	N	11585907
MGI:3037930	M	MP:0005578	teratozoospermia	Tnp2<tm1Mzh>/Tnp2<tm1Mzh>	involves: 129S/SvEv * 129S7/SvEvBrd	N	11585907
MGI:3037930	M	MP:0009232	abnormal sperm nucleus morphology	Tnp2<tm1Mzh>/Tnp2<tm1Mzh>	involves: 129S/SvEv * 129S7/SvEvBrd	N	11585907
MGI:3037930	M	MP:0009831	abnormal sperm midpiece morphology	Tnp2<tm1Mzh>/Tnp2<tm1Mzh>	involves: 129S/SvEv * 129S7/SvEvBrd	N	11585907
MGI:3037939	M	MP:0009231	detached acrosome	Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129S1/Sv * 129X1/SvJ	N	11385107
MGI:3037939	M	MP:0030976	impaired sperm penetration of zona pellucida	Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129S1/Sv * 129X1/SvJ	N	11385107
MGI:3037939	M	MP:0002675	asthenozoospermia	Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129S1/Sv * 129X1/SvJ	N	11385107
MGI:3037939	M	MP:0008898	abnormal acrosome morphology	Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129S1/Sv * 129X1/SvJ	N	11385107
MGI:3037939	M	MP:0009230	abnormal sperm head morphology	Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129S1/Sv * 129X1/SvJ	N	11385107
MGI:3037939	M	MP:0005578	teratozoospermia	Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129S1/Sv * 129X1/SvJ	N	11385107
MGI:3037939	M	MP:0001925	male infertility	Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129S1/Sv * 129X1/SvJ	N	11385107
MGI:3037950	F	MP:0005185	decreased circulating progesterone level	Pappa<tm1Cac>/Pappa<tm1Cac>	involves: 129 * C57BL/6	N	20130263
MGI:3037950	F	MP:0001262	decreased body weight	Pappa<tm1Cac>/Pappa<tm1Cac>	involves: 129 * C57BL/6	N	20130263
MGI:3037950	F	MP:0001127	small ovary	Pappa<tm1Cac>/Pappa<tm1Cac>	involves: 129 * C57BL/6	N	20130263
MGI:3037950	F	MP:0005181	decreased circulating estradiol level	Pappa<tm1Cac>/Pappa<tm1Cac>	involves: 129 * C57BL/6	N	20130263
MGI:3037950	F	MP:0001935	decreased litter size	Pappa<tm1Cac>/Pappa<tm1Cac>	involves: 129 * C57BL/6	N	20130263
MGI:3037950	F	MP:0001923	reduced female fertility	Pappa<tm1Cac>/Pappa<tm1Cac>	involves: 129 * C57BL/6	N	20130263
MGI:3037950	F	MP:0005319	abnormal enzyme/coenzyme level	Pappa<tm1Cac>/Pappa<tm1Cac>	involves: 129 * C57BL/6	N	20130263
MGI:3037950	F	MP:0005584	abnormal enzyme/coenzyme activity	Pappa<tm1Cac>/Pappa<tm1Cac>	involves: 129 * C57BL/6	N	20130263
MGI:3037950	F	MP:0004856	decreased ovary weight	Pappa<tm1Cac>/Pappa<tm1Cac>	involves: 129 * C57BL/6	N	20130263
MGI:3037950	F	MP:0031420	decreased superovulation rate	Pappa<tm1Cac>/Pappa<tm1Cac>	involves: 129 * C57BL/6	N	20130263
MGI:3037950	F	MP:0005182	increased circulating estradiol level	Pappa<tm1Cac>/Pappa<tm1Cac>	involves: 129 * C57BL/6	N	20130263
MGI:3037966	F	MP:0005397	hematopoietic system phenotype	Gata1<tm6Sho>/Gata1<tm6Sho>	involves: 129S1/Sv	Y	12045237
MGI:3037966	F	MP:0005012	decreased eosinophil cell number	Gata1<tm6Sho>/Gata1<tm6Sho>	involves: 129S1/Sv	N	12045237
MGI:3037970	M	MP:0005012	decreased eosinophil cell number	Gata1<tm6Sho>/Y	involves: 129S1/Sv	N	12045237
MGI:3037970	M	MP:0000208	decreased hematocrit	Gata1<tm6Sho>/Y	involves: 129S1/Sv	N	12045237
MGI:3037970	M	MP:0000691	enlarged spleen	Gata1<tm6Sho>/Y	involves: 129S1/Sv	N	12045237
MGI:3037970	M	MP:0002875	decreased erythrocyte cell number	Gata1<tm6Sho>/Y	involves: 129S1/Sv	N	12045237
MGI:3037970	M	MP:0005397	hematopoietic system phenotype	Gata1<tm6Sho>/Y	involves: 129S1/Sv	Y	12045237
MGI:3037984	M	MP:0002675	asthenozoospermia	Mak<tm1Yshk>/Mak<tm1Yshk>	B6.Cg-Mak<tm1Yshk>	N	11971961
MGI:3038110	M	MP:0008973	decreased erythroid progenitor cell number	Gata1<tm1Mym>/Y	involves: 129P2/OlaHsd * BALB/c	N	9139715
MGI:3038110	M	MP:0001698	decreased embryo size	Gata1<tm1Mym>/Y	involves: 129P2/OlaHsd * BALB/c	N	9139715
MGI:3038110	M	MP:0001722	pale yolk sac	Gata1<tm1Mym>/Y	involves: 129P2/OlaHsd * BALB/c	N	9139715
MGI:3038110	M	MP:0000603	pale liver	Gata1<tm1Mym>/Y	involves: 129P2/OlaHsd * BALB/c	N	9139715
MGI:3038110	M	MP:0004229	abnormal embryonic erythropoiesis	Gata1<tm1Mym>/Y	involves: 129P2/OlaHsd * BALB/c	N	9139715
MGI:3038110	M	MP:0001719	absent vitelline blood vessels	Gata1<tm1Mym>/Y	involves: 129P2/OlaHsd * BALB/c	N	9139715
MGI:3038110	M	MP:0001577	anemia	Gata1<tm1Mym>/Y	involves: 129P2/OlaHsd * BALB/c	N	9139715
MGI:3038110	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Gata1<tm1Mym>/Y	involves: 129P2/OlaHsd * BALB/c	N	9139715
MGI:3038111	F	MP:0001577	anemia	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd * BALB/c	N	9139715
MGI:3038111	F	MP:0000245	abnormal erythropoiesis	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd * BALB/c	N	9139715
MGI:3038120	F	MP:0000245	abnormal erythropoiesis	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd	N	9657742
MGI:3038120	F	MP:0009246	pale spleen	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd	N	9657742
MGI:3038120	F	MP:0003179	thrombocytopenia	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd	N	9657742
MGI:3038120	F	MP:0002083	premature death	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd	N	9657742
MGI:3038120	F	MP:0000240	extramedullary hematopoiesis	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd	N	9657742
MGI:3038120	F	MP:0000691	enlarged spleen	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd	N	9657742
MGI:3038120	F	MP:0002416	abnormal proerythroblast morphology	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd	N	9657742
MGI:3038120	F	MP:0001577	anemia	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd	N	9657742
MGI:3038120	F	MP:0008479	decreased spleen white pulp amount	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd	N	9657742
MGI:3038120	F	MP:0008477	decreased spleen red pulp amount	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd	N	9657742
MGI:3038120	F	MP:0002417	abnormal megakaryocyte morphology	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd	N	9657742
MGI:3038120	F	MP:0000208	decreased hematocrit	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd	N	9657742
MGI:3038120	F	MP:0008770	decreased survivor rate	Gata1<tm1Mym>/Gata1<+>	involves: 129P2/OlaHsd	N	9657742
MGI:3038250	F	MP:0010173	increased mammary gland epithelial cell proliferation	Ddr1<tm1Wfv>/Ddr1<tm1Wfv>	either: (involves: (129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	11283268
MGI:3038250	F	MP:0009503	abnormal mammary gland duct morphology	Ddr1<tm1Wfv>/Ddr1<tm1Wfv>	either: (involves: (129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	11283268
MGI:3038250	F	MP:0001728	failure of embryo implantation	Ddr1<tm1Wfv>/Ddr1<tm1Wfv>	either: (involves: (129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	11283268
MGI:3038250	F	MP:0001882	abnormal lactation	Ddr1<tm1Wfv>/Ddr1<tm1Wfv>	either: (involves: (129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	11283268
MGI:3038250	F	MP:0000628	abnormal mammary gland development	Ddr1<tm1Wfv>/Ddr1<tm1Wfv>	either: (involves: (129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	11283268
MGI:3038368	M	MP:0002566	abnormal sexual interaction	Rorb<tm1Mba>/Rorb<tm1Mba>	involves: 129P2/OlaHsd * C57BL/6	N	9670004
MGI:3038375	M	MP:0004542	impaired acrosome reaction	Plcd4<tm1Kfu>/Plcd4<tm1Kfu>	involves: 129X1/SvJ * C57BL/6J	N	12695499
MGI:3038375	M	MP:0004542	impaired acrosome reaction	Plcd4<tm1Kfu>/Plcd4<tm1Kfu>	involves: 129X1/SvJ * C57BL/6J	N	11340203
MGI:3038375	M	MP:0004543	abnormal sperm physiology	Plcd4<tm1Kfu>/Plcd4<tm1Kfu>	involves: 129X1/SvJ * C57BL/6J	N	12695499
MGI:3038375	M	MP:0001925	male infertility	Plcd4<tm1Kfu>/Plcd4<tm1Kfu>	involves: 129X1/SvJ * C57BL/6J	N	12695499
MGI:3038375	M	MP:0001925	male infertility	Plcd4<tm1Kfu>/Plcd4<tm1Kfu>	involves: 129X1/SvJ * C57BL/6J	N	11340203
MGI:3038416	F	MP:0008450	retina photoreceptor degeneration	Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6	N	10725384
MGI:3038416	F	MP:0008444	retina cone cell degeneration	Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6	N	12651948
MGI:3038416	F	MP:0008451	retina rod cell degeneration	Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6	N	12651948
MGI:3038416	F	MP:0008456	abnormal retina rod cell outer segment morphology	Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6	N	10725384
MGI:3038416	F	MP:0005253	abnormal eye physiology	Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6	N	10725384
MGI:3038416	F	MP:0001325	abnormal retina morphology	Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6	N	10725384
MGI:3038416	F	MP:0008587	short photoreceptor outer segment	Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6	N	10725384
MGI:3038416	F	MP:0008515	thin retina outer nuclear layer	Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6	N	10725384
MGI:3038416	F	MP:0001006	abnormal retina cone cell morphology	Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6	N	10725384
MGI:3038416	F	MP:0001326	retina degeneration	Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6	N	10725384
MGI:3038727	F	MP:0005253	abnormal eye physiology	Rpgr<tm1Tili>/Rpgr<tm1Tili>,Tg(CMV-Rpgr)1Tili/0	involves: 129S4/SvJae * C57BL/6	N	14691151
MGI:3038727	F	MP:0001325	abnormal retina morphology	Rpgr<tm1Tili>/Rpgr<tm1Tili>,Tg(CMV-Rpgr)1Tili/0	involves: 129S4/SvJae * C57BL/6	N	14691151
MGI:3038727	F	MP:0001326	retina degeneration	Rpgr<tm1Tili>/Rpgr<tm1Tili>,Tg(CMV-Rpgr)1Tili/0	involves: 129S4/SvJae * C57BL/6	N	14691151
MGI:3038845	M	MP:0003666	impaired sperm capacitation	Adcy10<tm1Lex>/Adcy10<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	16054031
MGI:3038845	M	MP:0001925	male infertility	Adcy10<tm1Lex>/Adcy10<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	14976244
MGI:3038845	M	MP:0009237	kinked sperm flagellum	Adcy10<tm1Lex>/Adcy10<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	16054031
MGI:3038845	M	MP:0005578	teratozoospermia	Adcy10<tm1Lex>/Adcy10<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	16054031
MGI:3038845	M	MP:0002675	asthenozoospermia	Adcy10<tm1Lex>/Adcy10<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	16054031
MGI:3038845	M	MP:0009243	hairpin sperm flagellum	Adcy10<tm1Lex>/Adcy10<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	16054031
MGI:3038845	M	MP:0002675	asthenozoospermia	Adcy10<tm1Lex>/Adcy10<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	14976244
MGI:3038845	M	MP:0001925	male infertility	Adcy10<tm1Lex>/Adcy10<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	16054031
MGI:3038845	M	MP:0002674	abnormal sperm motility	Adcy10<tm1Lex>/Adcy10<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	16054031
MGI:3039041	F	MP:0009687	empty decidua capsularis	Upf1<tm1Hcd>/Upf1<tm1Hcd>	involves: 129X1/SvJ * C57BL/6	N	11152657
MGI:3039123	F	MP:0001120	abnormal uterus morphology	Cacna2d2<ent>/Cacna2d2<ent>	either: B6.D2-Cacna2d2<ent> or (involves: C57BL/6J * CD-1 * DBA/2J)	N	14660671
MGI:3039123	F	MP:0001926	female infertility	Cacna2d2<ent>/Cacna2d2<ent>	either: B6.D2-Cacna2d2<ent> or (involves: C57BL/6J * CD-1 * DBA/2J)	N	14660671
MGI:3039123	M	MP:0002566	abnormal sexual interaction	Cacna2d2<ent>/Cacna2d2<ent>	either: B6.D2-Cacna2d2<ent> or (involves: C57BL/6J * CD-1 * DBA/2J)	N	14660671
MGI:3039357	F	MP:0009643	abnormal urine homeostasis	Renbp<tm1Csch>/Renbp<tm1Csch>	involves: 129 * C57BL/6J	N	10809771
MGI:3039357	F	MP:0005376	homeostasis/metabolism phenotype	Renbp<tm1Csch>/Renbp<tm1Csch>	involves: 129 * C57BL/6J	Y	10809771
MGI:3039361	F	MP:0001926	female infertility	Wnt7a<px-r>/Wnt7a<px-r>	involves: HR	N	MGI:3588414
MGI:3039379	F	MP:0001386	abnormal maternal nurturing	Rims1<tm1Sud>/Rims1<tm1Sud>	involves: 129P2/OlaHsd * C57BL/6	N	11797009
MGI:3039386	M	MP:0001925	male infertility	Ccna1<tm1Coll>/Ccna1<tm1Coll>	involves: 129S/SvEv * MF1	N	15047941
MGI:3039386	M	MP:0001155	arrest of spermatogenesis	Ccna1<tm1Coll>/Ccna1<tm1Coll>	involves: 129S/SvEv * MF1	N	15047941
MGI:3039386	M	MP:0004852	decreased testis weight	Ccna1<tm1Coll>/Ccna1<tm1Coll>	involves: 129S/SvEv * MF1	N	15047941
MGI:3039386	M	MP:0020550	multinucleated giant male germ cells	Ccna1<tm1Coll>/Ccna1<tm1Coll>	involves: 129S/SvEv * MF1	N	15047941
MGI:3039387	M	MP:0002687	oligozoospermia	Ccna1<tm1Coll>/Ccna1<+>	either: 129S/SvEv or (involves: 129S/SvEv * MF1)	N	15047941
MGI:3039387	M	MP:0001155	arrest of spermatogenesis	Ccna1<tm1Coll>/Ccna1<+>	either: 129S/SvEv or (involves: 129S/SvEv * MF1)	N	15047941
MGI:3039387	M	MP:0001922	reduced male fertility	Ccna1<tm1Coll>/Ccna1<+>	either: 129S/SvEv or (involves: 129S/SvEv * MF1)	N	15047941
MGI:3039402	F	MP:0001129	impaired ovarian folliculogenesis	Foxo3<Gt(VICTR20)1Kca>/Foxo3<Gt(VICTR20)1Kca>	involves: 129S5/SvEvBrd * C57BL/6	N	14978268
MGI:3039402	F	MP:0002682	decreased mature ovarian follicle number	Foxo3<Gt(VICTR20)1Kca>/Foxo3<Gt(VICTR20)1Kca>	involves: 129S5/SvEvBrd * C57BL/6	N	14978268
MGI:3039402	F	MP:0009093	oocyte degeneration	Foxo3<Gt(VICTR20)1Kca>/Foxo3<Gt(VICTR20)1Kca>	involves: 129S5/SvEvBrd * C57BL/6	N	14978268
MGI:3039404	F	MP:0002169	no abnormal phenotype detected	Foxo4<tm1Kca>/Foxo4<tm1Kca>	involves: 129X1/SvJ * C57BL/6	N	14978268
MGI:3039408	M	MP:0002169	no abnormal phenotype detected	Foxo4<tm1Kca>/Y	involves: 129X1/SvJ * C57BL/6	N	14978268
MGI:3039525	M	MP:0001922	reduced male fertility	Atp8b3<tm1Gar>/Atp8b3<tm1Gar>	involves: 129S/SvEv * C57BL/6J	N	14975727
MGI:3039525	M	MP:0004542	impaired acrosome reaction	Atp8b3<tm1Gar>/Atp8b3<tm1Gar>	involves: 129S/SvEv * C57BL/6J	N	14975727
MGI:3039549	F	MP:0001926	female infertility	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	N	9690472
MGI:3039549	F	MP:0001926	female infertility	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	N	16436621
MGI:3039679	M	MP:0002169	no abnormal phenotype detected	Eda2r<tm1Vmd>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	14749376
MGI:3039702	M	MP:0004852	decreased testis weight	Zfp110<tm1Mpin>/Zfp110<tm1Mpin>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	N	10545116
MGI:3039735	M	MP:0001153	small seminiferous tubules	Rbp1<tm1Ipc>/Rbp1<tm1Ipc>	involves: 129S2/SvPas	N	10487743
MGI:3039735	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Rbp1<tm1Ipc>/Rbp1<tm1Ipc>	involves: 129S2/SvPas	N	10487743
MGI:3039735	M	MP:0002216	abnormal seminiferous tubule morphology	Rbp1<tm1Ipc>/Rbp1<tm1Ipc>	involves: 129S2/SvPas	N	10487743
MGI:3039814	F	MP:0002637	small uterus	Rbms1<tm1Hiro>/Rbms1<tm1Hiro>	involves: C57BL/6 * CBA	N	11737267
MGI:3039826	M	MP:0005578	teratozoospermia	Prm1<tm1Eddy>/Prm1<+>	either: (chimera involves: 129P2/OlaHsd * C57BL/6N) or (chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6N)	N	11326282
MGI:3039826	M	MP:0020869	immotile sperm	Prm1<tm1Eddy>/Prm1<+>	either: (chimera involves: 129P2/OlaHsd * C57BL/6N) or (chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6N)	N	11326282
MGI:3039836	M	MP:0005578	teratozoospermia	Prm2<tm1Eddy>/Prm2<+>	either: (chimera involves: 129P2/OlaHsd * C57BL/6N) or (chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6N)	N	12620939
MGI:3039836	M	MP:0005578	teratozoospermia	Prm2<tm1Eddy>/Prm2<+>	either: (chimera involves: 129P2/OlaHsd * C57BL/6N) or (chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6N)	N	11326282
MGI:3039836	M	MP:0020869	immotile sperm	Prm2<tm1Eddy>/Prm2<+>	either: (chimera involves: 129P2/OlaHsd * C57BL/6N) or (chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6N)	N	11326282
MGI:3040073	F	MP:0001928	abnormal ovulation	Bfo/Bfo<+>	involves: BALB/cBy * C57BL/6By	N	4841379
MGI:3040262	F	MP:0002169	no abnormal phenotype detected	Arhgap6<tm1Hzo>/Arhgap6<tm1Hzo>	involves: 129S7/SvEvBrd * C57BL/6J	N	10699171
MGI:3040282	M	MP:0001925	male infertility	Dnmt3l<tm1Bes>/Dnmt3l<tm1Bes>	involves: 129S6/SvEvTac	N	11719692
MGI:3040282	M	MP:0004901	decreased male germ cell number	Dnmt3l<tm1Bes>/Dnmt3l<tm1Bes>	involves: 129S6/SvEvTac	N	17875220
MGI:3040282	M	MP:0005159	azoospermia	Dnmt3l<tm1Bes>/Dnmt3l<tm1Bes>	involves: 129S6/SvEvTac	N	11719692
MGI:3040282	M	MP:0001156	abnormal spermatogenesis	Dnmt3l<tm1Bes>/Dnmt3l<tm1Bes>	involves: 129S6/SvEvTac	N	17875220
MGI:3040282	F	MP:0001931	abnormal oogenesis	Dnmt3l<tm1Bes>/Dnmt3l<tm1Bes>	involves: 129S6/SvEvTac	N	11719692
MGI:3040282	F	MP:0001926	female infertility	Dnmt3l<tm1Bes>/Dnmt3l<tm1Bes>	involves: 129S6/SvEvTac	N	11719692
MGI:3040282	M	MP:0001147	small testis	Dnmt3l<tm1Bes>/Dnmt3l<tm1Bes>	involves: 129S6/SvEvTac	N	11719692
MGI:3040375	M	MP:0004852	decreased testis weight	Tswt<MSM/Ms>/Tswt<MSM/Ms>	involves: C57BL/6J * MSM/Ms	N	15020476
MGI:3040396	M	MP:0001153	small seminiferous tubules	H2ax<tm1Nus>/H2ax<tm1Nus>	Not Specified	N	11934988
MGI:3040396	M	MP:0008261	arrest of male meiosis	H2ax<tm1Nus>/H2ax<tm1Nus>	Not Specified	N	11934988
MGI:3040396	M	MP:0001147	small testis	H2ax<tm1Nus>/H2ax<tm1Nus>	Not Specified	N	11934988
MGI:3040406	M	MP:0003205	testicular atrophy	Cyct<tm1Jlm>/Cyct<tm1Jlm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12101247
MGI:3040406	M	MP:0002674	abnormal sperm motility	Cyct<tm1Jlm>/Cyct<tm1Jlm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12101247
MGI:3040406	M	MP:0002216	abnormal seminiferous tubule morphology	Cyct<tm1Jlm>/Cyct<tm1Jlm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12101247
MGI:3040406	M	MP:0001147	small testis	Cyct<tm1Jlm>/Cyct<tm1Jlm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12101247
MGI:3040406	M	MP:0002687	oligozoospermia	Cyct<tm1Jlm>/Cyct<tm1Jlm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12101247
MGI:3040459	M	MP:0001925	male infertility	Lvs/Lvs<+>	involves: BALB/cByJ * C57BL/6J * SJL/J	N	1946451
MGI:3040459	M	MP:0005578	teratozoospermia	Lvs/Lvs<+>	involves: BALB/cByJ * C57BL/6J * SJL/J	N	1946451
MGI:3040460	M	MP:0001925	male infertility	Lvs/Lvs<+>	involves: BALB/cByJ * C57BL/6J * FVB/N * SJL/J	N	1946451
MGI:3040460	M	MP:0005578	teratozoospermia	Lvs/Lvs<+>	involves: BALB/cByJ * C57BL/6J * FVB/N * SJL/J	N	1946451
MGI:3040618	F	MP:0002169	no abnormal phenotype detected	Ppef1<tm1Nat>/Ppef1<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11713293
MGI:3040619	M	MP:0002169	no abnormal phenotype detected	Ppef1<tm1Nat>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11713293
MGI:3040621	F	MP:0002169	no abnormal phenotype detected	Ppef1<tm1Nat>/Ppef1<tm1Nat>,Ppef2<tm1Nat>/Ppef2<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11713293
MGI:3040621	F	MP:0005391	vision/eye phenotype	Ppef1<tm1Nat>/Ppef1<tm1Nat>,Ppef2<tm1Nat>/Ppef2<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	11713293
MGI:3040622	M	MP:0005391	vision/eye phenotype	Ppef1<tm1Nat>/Y,Ppef2<tm1Nat>/Ppef2<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	11713293
MGI:3040622	M	MP:0002169	no abnormal phenotype detected	Ppef1<tm1Nat>/Y,Ppef2<tm1Nat>/Ppef2<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11713293
MGI:3040658	M	MP:0008261	arrest of male meiosis	Piwil1<tm1Hfl>/Piwil1<tm1Hfl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12062093
MGI:3040658	M	MP:0004852	decreased testis weight	Piwil1<tm1Hfl>/Piwil1<tm1Hfl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12062093
MGI:3040658	M	MP:0001925	male infertility	Piwil1<tm1Hfl>/Piwil1<tm1Hfl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12062093
MGI:3040658	M	MP:0006362	abnormal male germ cell morphology	Piwil1<tm1Hfl>/Piwil1<tm1Hfl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12062093
MGI:3040661	M	MP:0001925	male infertility	Crem<tm1Saco>/Crem<tm1Saco>	involves: C57BL/6	N	14757819
MGI:3040661	M	MP:0001155	arrest of spermatogenesis	Crem<tm1Saco>/Crem<tm1Saco>	involves: C57BL/6	N	14757819
MGI:3040663	M	MP:0005578	teratozoospermia	Crem<tm1Saco>/Crem<+>	involves: 129/Sv * C57BL/6	N	8600391
MGI:3040663	M	MP:0002687	oligozoospermia	Crem<tm1Saco>/Crem<+>	involves: 129/Sv * C57BL/6	N	8600391
MGI:3040663	M	MP:0001922	reduced male fertility	Crem<tm1Saco>/Crem<+>	involves: 129/Sv * C57BL/6	N	8600391
MGI:3040664	M	MP:0001158	abnormal prostate gland morphology	Mxi1<tm1Rdp>/Mxi1<tm1Rdp>	involves: 129/Sv * C57BL/6J * SJL	N	9624006
MGI:3040664	M	MP:0001167	prostate gland epithelial hyperplasia	Mxi1<tm1Rdp>/Mxi1<tm1Rdp>	involves: 129/Sv * C57BL/6J * SJL	N	9624006
MGI:3040868	F	MP:0001931	abnormal oogenesis	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	32086523
MGI:3040875	F	MP:0031381	decreased secondary ovarian follicle number	Ntrk2<tm1Rohr>/Ntrk2<tm1Rohr>	Not Specified	N	15013804
MGI:3040875	F	MP:0001129	impaired ovarian folliculogenesis	Ntrk2<tm1Rohr>/Ntrk2<tm1Rohr>	Not Specified	N	15013804
MGI:3040875	F	MP:0003357	impaired granulosa cell differentiation	Ntrk2<tm1Rohr>/Ntrk2<tm1Rohr>	Not Specified	N	15013804
MGI:3040875	F	MP:0031018	decreased granulosa cell proliferation	Ntrk2<tm1Rohr>/Ntrk2<tm1Rohr>	Not Specified	N	15013804
MGI:3040878	M	MP:0001147	small testis	Klhl10<tm1Zuk>/Klhl10<+>	chimera involves: 129S7/SvEvBrd * C57BL/6J	N	15136734
MGI:3040878	M	MP:0002216	abnormal seminiferous tubule morphology	Klhl10<tm1Zuk>/Klhl10<+>	chimera involves: 129S7/SvEvBrd * C57BL/6J	N	15136734
MGI:3040878	M	MP:0001155	arrest of spermatogenesis	Klhl10<tm1Zuk>/Klhl10<+>	chimera involves: 129S7/SvEvBrd * C57BL/6J	N	15136734
MGI:3040878	M	MP:0001925	male infertility	Klhl10<tm1Zuk>/Klhl10<+>	chimera involves: 129S7/SvEvBrd * C57BL/6J	N	15136734
MGI:3040878	M	MP:0001932	abnormal spermiogenesis	Klhl10<tm1Zuk>/Klhl10<+>	chimera involves: 129S7/SvEvBrd * C57BL/6J	N	15136734
MGI:3040878	M	MP:0002784	abnormal Sertoli cell morphology	Klhl10<tm1Zuk>/Klhl10<+>	chimera involves: 129S7/SvEvBrd * C57BL/6J	N	15136734
MGI:3040894	M	MP:0008280	abnormal male germ cell apoptosis	Zfp148<tm1Kii>/Zfp148<+>	Not Specified	N	12524542
MGI:3040894	M	MP:0001925	male infertility	Zfp148<tm1Kii>/Zfp148<+>	Not Specified	N	12524542
MGI:3040894	M	MP:0001147	small testis	Zfp148<tm1Kii>/Zfp148<+>	Not Specified	N	12524542
MGI:3040894	M	MP:0002216	abnormal seminiferous tubule morphology	Zfp148<tm1Kii>/Zfp148<+>	Not Specified	N	12524542
MGI:3040919	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Ocrl<tm1Nbm>	either: (involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6) or (involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6 * NIH Black Swiss) or (involves: 129S/SvEv * 129S6/SvEvTac * NIH Black Swiss)	N	9593760
MGI:3040920	M	MP:0002784	abnormal Sertoli cell morphology	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>	129/Sv-Inpp5b<tm1Nbm>	N	11967219
MGI:3040920	M	MP:0001925	male infertility	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>	129/Sv-Inpp5b<tm1Nbm>	N	11784089
MGI:3040920	M	MP:0001922	reduced male fertility	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>	129/Sv-Inpp5b<tm1Nbm>	N	11967219
MGI:3040920	M	MP:0002687	oligozoospermia	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>	129/Sv-Inpp5b<tm1Nbm>	N	11784089
MGI:3040920	M	MP:0001156	abnormal spermatogenesis	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>	129/Sv-Inpp5b<tm1Nbm>	N	11967219
MGI:3040920	M	MP:0002675	asthenozoospermia	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>	129/Sv-Inpp5b<tm1Nbm>	N	11784089
MGI:3040922	M	MP:0001922	reduced male fertility	Inpp5b<tm2.1Nbm>/Inpp5b<tm2.1Nbm>	involves: 129S6/SvEvTac * FVB/N	N	11784089
MGI:3040922	M	MP:0001925	male infertility	Inpp5b<tm2.1Nbm>/Inpp5b<tm2.1Nbm>	involves: 129S6/SvEvTac * FVB/N	N	11784089
MGI:3040925	M	MP:0001932	abnormal spermiogenesis	Ift56<hop>/Ift56<hop>	Not Specified	N	5088020
MGI:3040925	M	MP:0009376	abnormal manchette morphology	Ift56<hop>/Ift56<hop>	Not Specified	N	9674995
MGI:3040925	M	MP:0005159	azoospermia	Ift56<hop>/Ift56<hop>	Not Specified	N	9674995
MGI:3040925	M	MP:0008545	absent sperm flagellum	Ift56<hop>/Ift56<hop>	Not Specified	N	5088020
MGI:3040925	M	MP:0001932	abnormal spermiogenesis	Ift56<hop>/Ift56<hop>	Not Specified	N	9674995
MGI:3040925	M	MP:0006380	abnormal spermatid morphology	Ift56<hop>/Ift56<hop>	Not Specified	N	5088020
MGI:3040925	M	MP:0008892	abnormal sperm flagellum morphology	Ift56<hop>/Ift56<hop>	Not Specified	N	5088020
MGI:3040925	M	MP:0005169	abnormal male meiosis	Ift56<hop>/Ift56<hop>	Not Specified	N	5088020
MGI:3040925	M	MP:0001147	small testis	Ift56<hop>/Ift56<hop>	Not Specified	N	5088020
MGI:3040925	M	MP:0001925	male infertility	Ift56<hop>/Ift56<hop>	Not Specified	N	9674995
MGI:3040925	M	MP:0005159	azoospermia	Ift56<hop>/Ift56<hop>	Not Specified	N	5088020
MGI:3040925	M	MP:0001925	male infertility	Ift56<hop>/Ift56<hop>	Not Specified	N	5088020
MGI:3040931	M	MP:0005578	teratozoospermia	t<w2>/t<w2>	Not Specified	N	9674995
MGI:3040931	M	MP:0001925	male infertility	t<w2>/t<w2>	Not Specified	N	9674995
MGI:3040931	M	MP:0001154	seminiferous tubule degeneration	t<w2>/t<w2>	Not Specified	N	9674995
MGI:3040931	M	MP:0009376	abnormal manchette morphology	t<w2>/t<w2>	Not Specified	N	9674995
MGI:3040932	M	MP:0001925	male infertility	t<w8>/t<w8>	Not Specified	N	9674995
MGI:3040932	M	MP:0005578	teratozoospermia	t<w8>/t<w8>	Not Specified	N	9674995
MGI:3040932	M	MP:0031374	abnormal manchette assembly	t<w8>/t<w8>	Not Specified	N	9674995
MGI:3040932	M	MP:0009230	abnormal sperm head morphology	t<w8>/t<w8>	Not Specified	N	9674995
MGI:3040932	M	MP:0001154	seminiferous tubule degeneration	t<w8>/t<w8>	Not Specified	N	9674995
MGI:3040932	M	MP:0009232	abnormal sperm nucleus morphology	t<w8>/t<w8>	Not Specified	N	9674995
MGI:3040934	M	MP:0002784	abnormal Sertoli cell morphology	Fndc3a<sys>/Fndc3a<sys>	involves: C3H * FVB/N	N	2164218
MGI:3040934	M	MP:0001925	male infertility	Fndc3a<sys>/Fndc3a<sys>	involves: C3H * FVB/N	N	1759682
MGI:3040934	M	MP:0001925	male infertility	Fndc3a<sys>/Fndc3a<sys>	involves: C3H * FVB/N	N	2164218
MGI:3040934	M	MP:0004852	decreased testis weight	Fndc3a<sys>/Fndc3a<sys>	involves: C3H * FVB/N	N	2164218
MGI:3040934	M	MP:0001155	arrest of spermatogenesis	Fndc3a<sys>/Fndc3a<sys>	involves: C3H * FVB/N	N	1759682
MGI:3040934	M	MP:0020550	multinucleated giant male germ cells	Fndc3a<sys>/Fndc3a<sys>	involves: C3H * FVB/N	N	2164218
MGI:3040934	M	MP:0004852	decreased testis weight	Fndc3a<sys>/Fndc3a<sys>	involves: C3H * FVB/N	N	1759682
MGI:3040934	M	MP:0002784	abnormal Sertoli cell morphology	Fndc3a<sys>/Fndc3a<sys>	involves: C3H * FVB/N	N	1759682
MGI:3040934	M	MP:0002216	abnormal seminiferous tubule morphology	Fndc3a<sys>/Fndc3a<sys>	involves: C3H * FVB/N	N	1759682
MGI:3040934	M	MP:0001155	arrest of spermatogenesis	Fndc3a<sys>/Fndc3a<sys>	involves: C3H * FVB/N	N	2164218
MGI:3040936	F	MP:0001930	abnormal meiosis	Poo/Poo	involves: C57BL/Ws * LT/SvKau	N	8157170
MGI:3040936	F	MP:0001928	abnormal ovulation	Poo/Poo	involves: C57BL/Ws * LT/SvKau	N	8157170
MGI:3040938	F	MP:0001928	abnormal ovulation	Poo/Poo<+>	involves: C57BL/Ws * LT/SvKau	N	8157170
MGI:3041122	F	MP:0005379	endocrine/exocrine gland phenotype	Nrip1<tm1Mpk>/Nrip1<+>	involves: 129/Ola	Y	11100122
MGI:3041122	F	MP:0001928	abnormal ovulation	Nrip1<tm1Mpk>/Nrip1<+>	involves: 129/Ola	N	11100122
MGI:3041122	F	MP:0031422	failure of superovulation	Nrip1<tm1Mpk>/Nrip1<+>	involves: 129/Ola	N	11100122
MGI:3041122	F	MP:0009648	abnormal superovulation	Nrip1<tm1Mpk>/Nrip1<+>	involves: 129/Ola	N	11100122
MGI:3041140	F	MP:0001384	abnormal pup retrieval	Map6<tm1Job>/Map6<tm1Job>	either: 129S2/SvPas or (involves: 129S2/SvPas * BALB/c)	N	12231625
MGI:3041147	F	MP:0003995	abnormal uterine artery morphology	Nos2<tm1Mrl>/Nos2<tm1Mrl>	involves: 129S7/SvEvBrd * C57BL/6	N	12090918
MGI:3041147	F	MP:0001120	abnormal uterus morphology	Nos2<tm1Mrl>/Nos2<tm1Mrl>	involves: 129S7/SvEvBrd * C57BL/6	N	12090918
MGI:3041147	F	MP:0009011	prolonged diestrus	Nos2<tm1Mrl>/Nos2<tm1Mrl>	involves: 129S7/SvEvBrd * C57BL/6	N	10377046
MGI:3041154	F	MP:0009006	prolonged estrous cycle	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae * C57BL/6J	N	10377046
MGI:3041154	F	MP:0009011	prolonged diestrus	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae * C57BL/6J	N	10377046
MGI:3041154	F	MP:0003355	decreased ovulation rate	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae * C57BL/6J	N	10377046
MGI:3041262	F	MP:0008976	delayed female fertility	Nos3<tm1Weo>/Nos3<tm1Weo>	B6.129S7-Nos3<tm1Weo>	N	10785232
MGI:3041262	F	MP:0031420	decreased superovulation rate	Nos3<tm1Weo>/Nos3<tm1Weo>	B6.129S7-Nos3<tm1Weo>	N	10785232
MGI:3041262	F	MP:0009648	abnormal superovulation	Nos3<tm1Weo>/Nos3<tm1Weo>	B6.129S7-Nos3<tm1Weo>	N	10785232
MGI:3041262	F	MP:0031420	decreased superovulation rate	Nos3<tm1Weo>/Nos3<tm1Weo>	B6.129S7-Nos3<tm1Weo>	N	11779605
MGI:3041262	F	MP:0008995	early reproductive senescence	Nos3<tm1Weo>/Nos3<tm1Weo>	B6.129S7-Nos3<tm1Weo>	N	10785232
MGI:3041262	F	MP:0002161	abnormal fertility/fecundity	Nos3<tm1Weo>/Nos3<tm1Weo>	B6.129S7-Nos3<tm1Weo>	N	10785232
MGI:3041396	F	MP:0003631	nervous system phenotype	L1cam<tm1.1Vlem>/L1cam<tm1.1Vlem>	129S2.Cg-L1cam<tm1.1Vlem>	Y	15067019
MGI:3041396	F	MP:0011101	prenatal lethality, incomplete penetrance	L1cam<tm1.1Vlem>/L1cam<tm1.1Vlem>	129S2.Cg-L1cam<tm1.1Vlem>	N	15067019
MGI:3041397	M	MP:0005578	teratozoospermia	Ift56<hop-hpy>/Ift56<hop-hpy>	Not Specified	N	MGI:63094
MGI:3041397	M	MP:0001932	abnormal spermiogenesis	Ift56<hop-hpy>/Ift56<hop-hpy>	Not Specified	N	MGI:63094
MGI:3041397	M	MP:0001925	male infertility	Ift56<hop-hpy>/Ift56<hop-hpy>	Not Specified	N	MGI:63094
MGI:3041397	M	MP:0002784	abnormal Sertoli cell morphology	Ift56<hop-hpy>/Ift56<hop-hpy>	Not Specified	N	872193
MGI:3041397	M	MP:0005578	teratozoospermia	Ift56<hop-hpy>/Ift56<hop-hpy>	Not Specified	N	872193
MGI:3041397	M	MP:0001925	male infertility	Ift56<hop-hpy>/Ift56<hop-hpy>	Not Specified	N	872193
MGI:3041397	M	MP:0001932	abnormal spermiogenesis	Ift56<hop-hpy>/Ift56<hop-hpy>	Not Specified	N	872193
MGI:3041397	M	MP:0001925	male infertility	Ift56<hop-hpy>/Ift56<hop-hpy>	Not Specified	N	MGI:1889021
MGI:3041398	F	MP:0001891	hydrocephaly	L1cam<tm1.1Vlem>/L1cam<tm1.1Vlem>	B6.Cg-L1cam<tm1.1Vlem>	N	15067019
MGI:3041398	F	MP:0011101	prenatal lethality, incomplete penetrance	L1cam<tm1.1Vlem>/L1cam<tm1.1Vlem>	B6.Cg-L1cam<tm1.1Vlem>	N	15067019
MGI:3041398	F	MP:0011085	postnatal lethality, complete penetrance	L1cam<tm1.1Vlem>/L1cam<tm1.1Vlem>	B6.Cg-L1cam<tm1.1Vlem>	N	15067019
MGI:3041444	M	MP:0001925	male infertility	Ift56<hop-hpy>/Ift56<hop-hpy>,Oca2<p-s>/Oca2<p-s>	Not Specified	N	7317942
MGI:3041444	M	MP:0001932	abnormal spermiogenesis	Ift56<hop-hpy>/Ift56<hop-hpy>,Oca2<p-s>/Oca2<p-s>	Not Specified	N	7317942
MGI:3041444	M	MP:0005578	teratozoospermia	Ift56<hop-hpy>/Ift56<hop-hpy>,Oca2<p-s>/Oca2<p-s>	Not Specified	N	7317942
MGI:3041455	M	MP:0001932	abnormal spermiogenesis	Oca2<p-s>/Oca2<p-s>	Not Specified	N	14402638
MGI:3041455	M	MP:0005578	teratozoospermia	Oca2<p-s>/Oca2<p-s>	Not Specified	N	14402638
MGI:3041455	F	MP:0001386	abnormal maternal nurturing	Oca2<p-s>/Oca2<p-s>	Not Specified	N	14402638
MGI:3041455	M	MP:0001925	male infertility	Oca2<p-s>/Oca2<p-s>	Not Specified	N	14402638
MGI:3041533	M	MP:0001925	male infertility	Mitf<mi-enu5>/Mitf<mi-enu5>	involves: 102 * C3H/El	N	15081122
MGI:3041533	F	MP:0001382	abnormal nursing	Mitf<mi-enu5>/Mitf<mi-enu5>	involves: 102 * C3H/El	N	15081122
MGI:3041533	F	MP:0001926	female infertility	Mitf<mi-enu5>/Mitf<mi-enu5>	involves: 102 * C3H/El	N	15081122
MGI:3041536	F	MP:0001926	female infertility	Mitf<mi-Mhdabcc2>/Mitf<mi-Mhdabcc2>	C3HeB/FeJ-Mitf<mi-Mhdabcc2>/Ieg	N	15081122
MGI:3041536	F	MP:0001382	abnormal nursing	Mitf<mi-Mhdabcc2>/Mitf<mi-Mhdabcc2>	C3HeB/FeJ-Mitf<mi-Mhdabcc2>/Ieg	N	15081122
MGI:3041536	M	MP:0001925	male infertility	Mitf<mi-Mhdabcc2>/Mitf<mi-Mhdabcc2>	C3HeB/FeJ-Mitf<mi-Mhdabcc2>/Ieg	N	15081122
MGI:3041539	F	MP:0002761	abnormal hippocampal mossy fiber morphology	Plxna3<tm1Matl>/Plxna3<tm1Matl>	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	11683995
MGI:3041539	F	MP:0002961	abnormal axon guidance	Plxna3<tm1Matl>/Plxna3<tm1Matl>	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	11683995
MGI:3041539	F	MP:0001065	abnormal trigeminal nerve morphology	Plxna3<tm1Matl>/Plxna3<tm1Matl>	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	11683995
MGI:3041539	F	MP:0000815	abnormal Ammon gyrus morphology	Plxna3<tm1Matl>/Plxna3<tm1Matl>	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	11683995
MGI:3041539	F	MP:0002761	abnormal hippocampal mossy fiber morphology	Plxna3<tm1Matl>/Plxna3<tm1Matl>	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	12732138
MGI:3041539	F	MP:0000807	abnormal hippocampus morphology	Plxna3<tm1Matl>/Plxna3<tm1Matl>	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	11683995
MGI:3041539	F	MP:0008960	abnormal axon pruning	Plxna3<tm1Matl>/Plxna3<tm1Matl>	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	12732138
MGI:3041540	M	MP:0002761	abnormal hippocampal mossy fiber morphology	Plxna3<tm1Matl>/Y	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	11683995
MGI:3041540	M	MP:0001065	abnormal trigeminal nerve morphology	Plxna3<tm1Matl>/Y	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	11683995
MGI:3041540	M	MP:0002961	abnormal axon guidance	Plxna3<tm1Matl>/Y	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	11683995
MGI:3041540	M	MP:0000815	abnormal Ammon gyrus morphology	Plxna3<tm1Matl>/Y	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	11683995
MGI:3041540	M	MP:0008960	abnormal axon pruning	Plxna3<tm1Matl>/Y	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	12732138
MGI:3041540	M	MP:0000807	abnormal hippocampus morphology	Plxna3<tm1Matl>/Y	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	11683995
MGI:3041540	M	MP:0002761	abnormal hippocampal mossy fiber morphology	Plxna3<tm1Matl>/Y	either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1)	N	12732138
MGI:3041941	M	MP:0001925	male infertility	Dnah1<tm1Ihgg>/Dnah1<tm1Ihgg>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	11371505
MGI:3041941	M	MP:0002675	asthenozoospermia	Dnah1<tm1Ihgg>/Dnah1<tm1Ihgg>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	11371505
MGI:3042112	F	MP:0001926	female infertility	Arnt<tm1Bra>/Arnt<tm1Bra>	B6.129-Arnt<tm1Bra>	N	14764592
MGI:3042181	M	MP:0002784	abnormal Sertoli cell morphology	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	8895659
MGI:3042181	M	MP:0001922	reduced male fertility	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	8895659
MGI:3042181	M	MP:0001925	male infertility	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	8895659
MGI:3042181	M	MP:0001152	increased Leydig cell number	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	8895659
MGI:3042181	F	MP:0005389	reproductive system phenotype	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	Y	8895659
MGI:3042181	M	MP:0001154	seminiferous tubule degeneration	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	8895659
MGI:3042181	M	MP:0002789	male pseudohermaphroditism	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd * C57BL/6	N	8895659
MGI:3042182	M	MP:0001154	seminiferous tubule degeneration	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd	N	8895659
MGI:3042182	M	MP:0001152	increased Leydig cell number	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd	N	8895659
MGI:3042182	M	MP:0002789	male pseudohermaphroditism	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd	N	8895659
MGI:3042182	M	MP:0001925	male infertility	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd	N	8895659
MGI:3042182	M	MP:0001922	reduced male fertility	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd	N	8895659
MGI:3042182	F	MP:0005389	reproductive system phenotype	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd	Y	8895659
MGI:3042182	M	MP:0002784	abnormal Sertoli cell morphology	Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	involves: 129S7/SvEvBrd	N	8895659
MGI:3042185	F	MP:0005389	reproductive system phenotype	Amh<tm1Bhr>/Amh<tm1Bhr>,Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	Not Specified	Y	8895659
MGI:3042185	M	MP:0001925	male infertility	Amh<tm1Bhr>/Amh<tm1Bhr>,Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	Not Specified	N	8895659
MGI:3042185	M	MP:0002789	male pseudohermaphroditism	Amh<tm1Bhr>/Amh<tm1Bhr>,Amhr2<tm1Bhr>/Amhr2<tm1Bhr>	Not Specified	N	8895659
MGI:3042186	F	MP:0002833	increased heart weight	Lamp2<tm1Psa>/Lamp2<tm1Psa>	either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv)	N	10972293
MGI:3042186	F	MP:0005311	abnormal circulating amino acid level	Lamp2<tm1Psa>/Lamp2<tm1Psa>	either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv)	N	10972293
MGI:3042186	F	MP:0001935	decreased litter size	Lamp2<tm1Psa>/Lamp2<tm1Psa>	either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv)	N	10972293
MGI:3042186	F	MP:0005140	decreased cardiac muscle contractility	Lamp2<tm1Psa>/Lamp2<tm1Psa>	either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv)	N	10972293
MGI:3042186	F	MP:0002083	premature death	Lamp2<tm1Psa>/Lamp2<tm1Psa>	either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv)	N	10972293
MGI:3042186	F	MP:0001262	decreased body weight	Lamp2<tm1Psa>/Lamp2<tm1Psa>	either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv)	N	10972293
MGI:3042186	F	MP:0005621	abnormal cell physiology	Lamp2<tm1Psa>/Lamp2<tm1Psa>	either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv)	N	10972293
MGI:3042186	F	MP:0008475	intermingled spleen red and white pulp	Lamp2<tm1Psa>/Lamp2<tm1Psa>	either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv)	N	10972293
MGI:3042186	F	MP:0000703	abnormal thymus morphology	Lamp2<tm1Psa>/Lamp2<tm1Psa>	either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv)	N	10972293
MGI:3042263	F	MP:0001619	abnormal vascular permeability	Nr4a1<tm1Jmi>/Nr4a1<tm1Jmi>	involves: 129S2/SvPas	N	24485460
MGI:3042263	F	MP:0009671	abnormal uterus physiology	Nr4a1<tm1Jmi>/Nr4a1<tm1Jmi>	involves: 129S2/SvPas	N	24485460
MGI:3042272	F	MP:0001923	reduced female fertility	Gh<Sma1>/Gh<Sma1>	C3HeB/FeJ-Gh<Sma1>	N	14726450
MGI:3042275	F	MP:0004834	ovary hemorrhage	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Fst<tm1Zuk>/Fst<tm2Zuk>	involves: 129S/SvEv * C57BL/6J	N	14701941
MGI:3042275	F	MP:0002680	decreased corpora lutea number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Fst<tm1Zuk>/Fst<tm2Zuk>	involves: 129S/SvEv * C57BL/6J	N	14701941
MGI:3042275	F	MP:0001923	reduced female fertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Fst<tm1Zuk>/Fst<tm2Zuk>	involves: 129S/SvEv * C57BL/6J	N	14701941
MGI:3042275	F	MP:0002016	ovary cyst	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Fst<tm1Zuk>/Fst<tm2Zuk>	involves: 129S/SvEv * C57BL/6J	N	14701941
MGI:3042275	F	MP:0001126	abnormal ovary morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Fst<tm1Zuk>/Fst<tm2Zuk>	involves: 129S/SvEv * C57BL/6J	N	14701941
MGI:3042275	F	MP:0001926	female infertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Fst<tm1Zuk>/Fst<tm2Zuk>	involves: 129S/SvEv * C57BL/6J	N	14701941
MGI:3042275	F	MP:0011129	decreased tertiary ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Fst<tm1Zuk>/Fst<tm2Zuk>	involves: 129S/SvEv * C57BL/6J	N	14701941
MGI:3042275	F	MP:0031420	decreased superovulation rate	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Fst<tm1Zuk>/Fst<tm2Zuk>	involves: 129S/SvEv * C57BL/6J	N	14701941
MGI:3042280	M	MP:0005331	insulin resistance	Rps6ka3<tm1Ljg>/Y	involves: 129 * C57BL/6	N	12765942
MGI:3042280	M	MP:0002079	increased circulating insulin level	Rps6ka3<tm1Ljg>/Y	involves: 129 * C57BL/6	N	12765942
MGI:3042280	M	MP:0005293	impaired glucose tolerance	Rps6ka3<tm1Ljg>/Y	involves: 129 * C57BL/6	N	12765942
MGI:3042280	M	MP:0005668	decreased circulating leptin level	Rps6ka3<tm1Ljg>/Y	involves: 129 * C57BL/6	N	12765942
MGI:3042280	M	MP:0005559	increased circulating glucose level	Rps6ka3<tm1Ljg>/Y	involves: 129 * C57BL/6	N	12765942
MGI:3042280	M	MP:0002063	abnormal learning/memory/conditioning	Rps6ka3<tm1Ljg>/Y	involves: 129 * C57BL/6	N	11113183
MGI:3042280	M	MP:0001262	decreased body weight	Rps6ka3<tm1Ljg>/Y	involves: 129 * C57BL/6	N	12765942
MGI:3042280	M	MP:0001924	infertility	Rps6ka3<tm1Ljg>/Y	involves: 129 * C57BL/6	N	12765942
MGI:3042280	M	MP:0001783	decreased white adipose tissue amount	Rps6ka3<tm1Ljg>/Y	involves: 129 * C57BL/6	N	12765942
MGI:3042280	M	MP:0001405	impaired coordination	Rps6ka3<tm1Ljg>/Y	involves: 129 * C57BL/6	N	11113183
MGI:3042280	M	MP:0001258	decreased body length	Rps6ka3<tm1Ljg>/Y	involves: 129 * C57BL/6	N	11113183
MGI:3042280	M	MP:0010399	decreased skeletal muscle glycogen level	Rps6ka3<tm1Ljg>/Y	involves: 129 * C57BL/6	N	11113183
MGI:3042280	M	MP:0001265	decreased body size	Rps6ka3<tm1Ljg>/Y	involves: 129 * C57BL/6	N	11113183
MGI:3042281	F	MP:0001924	infertility	Rps6ka3<tm1Ljg>/Rps6ka3<tm1Ljg>	involves: 129 * C57BL/6	N	12765942
MGI:3042292	F	MP:0001923	reduced female fertility	Gh<Sma1>/Gh<+>	C3HeB/FeJ-Gh<Sma1>	N	14726450
MGI:3042587	F	MP:0005386	behavior/neurological phenotype	Maob<tm1Shih>/Maob<tm1Shih>	either: (involves: 129S/SvEv) or (involves: 129S4/SvJae)	Y	9326944
MGI:3042587	F	MP:0005376	homeostasis/metabolism phenotype	Maob<tm1Shih>/Maob<tm1Shih>	either: (involves: 129S/SvEv) or (involves: 129S4/SvJae)	Y	9326944
MGI:3042587	F	MP:0031391	increased locomotor activity	Maob<tm1Shih>/Maob<tm1Shih>	either: (involves: 129S/SvEv) or (involves: 129S4/SvJae)	N	9326944
MGI:3042587	F	MP:0009643	abnormal urine homeostasis	Maob<tm1Shih>/Maob<tm1Shih>	either: (involves: 129S/SvEv) or (involves: 129S4/SvJae)	N	9326944
MGI:3042587	F	MP:0011452	decreased susceptibility to dopaminergic neuron neurotoxicity	Maob<tm1Shih>/Maob<tm1Shih>	either: (involves: 129S/SvEv) or (involves: 129S4/SvJae)	N	9326944
MGI:3042593	M	MP:0004901	decreased male germ cell number	Zbtb16<lu>/Zbtb16<lu>	B6.C3-Zbtb16<Lu>	N	15156142
MGI:3042593	M	MP:0001147	small testis	Zbtb16<lu>/Zbtb16<lu>	B6.C3-Zbtb16<Lu>	N	15156142
MGI:3042593	M	MP:0005159	azoospermia	Zbtb16<lu>/Zbtb16<lu>	B6.C3-Zbtb16<Lu>	N	15156142
MGI:3042594	M	MP:0005159	azoospermia	Zbtb16<lu>/Zbtb16<lu>	Not Specified	N	5088020
MGI:3042594	M	MP:0001925	male infertility	Zbtb16<lu>/Zbtb16<lu>	Not Specified	N	5088020
MGI:3042606	F	MP:0001127	small ovary	Prop1<df>/Prop1<df>	STOCK Prop1<df>	N	14173795
MGI:3042606	F	MP:0001134	absent corpus luteum	Prop1<df>/Prop1<df>	STOCK Prop1<df>	N	14173795
MGI:3042606	F	MP:0001926	female infertility	Prop1<df>/Prop1<df>	STOCK Prop1<df>	N	8934515
MGI:3042606	F	MP:0011130	absent tertiary ovarian follicles	Prop1<df>/Prop1<df>	STOCK Prop1<df>	N	14173795
MGI:3042606	M	MP:0001925	male infertility	Prop1<df>/Prop1<df>	STOCK Prop1<df>	N	8934515
MGI:3042846	F	MP:0008574	decreased circulating interferon-alpha level	Tlr7<tm1Flv>/Tlr7<tm1Flv>	involves: 129S1/Sv	N	15034168
MGI:3043062	M	MP:0001156	abnormal spermatogenesis	Dms/Dms<+>	involves: C57BL/6 * DBA/2	N	11870080
MGI:3043062	M	MP:0005159	azoospermia	Dms/Dms<+>	involves: C57BL/6 * DBA/2	N	11870080
MGI:3043062	M	MP:0001146	abnormal testis morphology	Dms/Dms<+>	involves: C57BL/6 * DBA/2	N	11870080
MGI:3043062	M	MP:0001925	male infertility	Dms/Dms<+>	involves: C57BL/6 * DBA/2	N	11870080
MGI:3043062	M	MP:0001932	abnormal spermiogenesis	Dms/Dms<+>	involves: C57BL/6 * DBA/2	N	11870080
MGI:3043062	M	MP:0001145	abnormal male reproductive system morphology	Dms/Dms<+>	involves: C57BL/6 * DBA/2	N	11870080
MGI:3043062	M	MP:0008261	arrest of male meiosis	Dms/Dms<+>	involves: C57BL/6 * DBA/2	N	11870080
MGI:3043197	F	MP:0005388	respiratory system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0004610	small vertebrae	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	N	15109498
MGI:3043197	F	MP:0008271	abnormal bone ossification	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	N	15109498
MGI:3043197	F	MP:0005387	immune system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0005385	cardiovascular system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0005391	vision/eye phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0005389	reproductive system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0005367	renal/urinary system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0030029	wide cranial sutures	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	N	15109498
MGI:3043197	F	MP:0005369	muscle phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0005377	hearing/vestibular/ear phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0005006	abnormal osteoblast physiology	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	N	15109498
MGI:3043197	F	MP:0000063	decreased bone mineral density	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	N	15109498
MGI:3043197	F	MP:0004418	small parietal bone	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	N	15109498
MGI:3043197	F	MP:0005370	liver/biliary system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0005397	hematopoietic system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0004384	small interparietal bone	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	N	15109498
MGI:3043197	F	MP:0004377	small frontal bone	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	N	15109498
MGI:3043197	F	MP:0003631	nervous system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0030388	large fontanelles	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	N	15109498
MGI:3043197	F	MP:0005394	taste/olfaction phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0005379	endocrine/exocrine gland phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0002896	abnormal bone mineralization	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	N	15109498
MGI:3043197	F	MP:0004686	decreased length of long bones	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	N	15109498
MGI:3043197	F	MP:0004016	decreased bone mass	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	N	15109498
MGI:3043197	F	MP:0010771	integument phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043197	F	MP:0010869	decreased bone trabecula number	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	N	15109498
MGI:3043197	F	MP:0005381	digestive/alimentary phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<tm1.1Kry>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0004384	small interparietal bone	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	N	15109498
MGI:3043224	F	MP:0004377	small frontal bone	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	N	15109498
MGI:3043224	F	MP:0008271	abnormal bone ossification	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	N	15109498
MGI:3043224	F	MP:0005391	vision/eye phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0030029	wide cranial sutures	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	N	15109498
MGI:3043224	F	MP:0004418	small parietal bone	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	N	15109498
MGI:3043224	F	MP:0004686	decreased length of long bones	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	N	15109498
MGI:3043224	F	MP:0005385	cardiovascular system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0005379	endocrine/exocrine gland phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0004016	decreased bone mass	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	N	15109498
MGI:3043224	F	MP:0005367	renal/urinary system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0002896	abnormal bone mineralization	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	N	15109498
MGI:3043224	F	MP:0005394	taste/olfaction phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0005006	abnormal osteoblast physiology	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	N	15109498
MGI:3043224	F	MP:0005369	muscle phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0005388	respiratory system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0004610	small vertebrae	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	N	15109498
MGI:3043224	F	MP:0005387	immune system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0010771	integument phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0005370	liver/biliary system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0005381	digestive/alimentary phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0003631	nervous system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0005377	hearing/vestibular/ear phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0030388	large fontanelles	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	N	15109498
MGI:3043224	F	MP:0005389	reproductive system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0005397	hematopoietic system phenotype	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	Y	15109498
MGI:3043224	F	MP:0000063	decreased bone mineral density	Rps6ka3<tm1.1Kry>/Rps6ka3<+>	involves: 129X1/SvJ	N	15109498
MGI:3043294	F	MP:0001926	female infertility	Atf4<tm1Tow>/Atf4<tm1Tow>	involves: 129S1/Sv * 129X1/SvJ * NIH Black Swiss	N	11806972
MGI:3043294	M	MP:0001922	reduced male fertility	Atf4<tm1Tow>/Atf4<tm1Tow>	involves: 129S1/Sv * 129X1/SvJ * NIH Black Swiss	N	11806972
MGI:3043294	M	MP:0001925	male infertility	Atf4<tm1Tow>/Atf4<tm1Tow>	involves: 129S1/Sv * 129X1/SvJ * NIH Black Swiss	N	11806972
MGI:3043301	F	MP:0003631	nervous system phenotype	Mapt<tm1(Mecp2)Jae>/Mapt<+>,Mecp2<tm1.1Jae>/Mecp2<+>	involves: 129S4/SvJae * C57BL/6	Y	15069197
MGI:3043301	F	MP:0005378	growth/size/body region phenotype	Mapt<tm1(Mecp2)Jae>/Mapt<+>,Mecp2<tm1.1Jae>/Mecp2<+>	involves: 129S4/SvJae * C57BL/6	Y	15069197
MGI:3043301	F	MP:0005386	behavior/neurological phenotype	Mapt<tm1(Mecp2)Jae>/Mapt<+>,Mecp2<tm1.1Jae>/Mecp2<+>	involves: 129S4/SvJae * C57BL/6	Y	15069197
MGI:3043303	F	MP:0001402	decreased locomotor activity	Mecp2<tm1.1Jae>/Mecp2<+>	involves: 129S4/SvJae * C57BL/6	N	15069197
MGI:3043303	F	MP:0001262	decreased body weight	Mecp2<tm1.1Jae>/Mecp2<+>	involves: 129S4/SvJae * C57BL/6	N	15069197
MGI:3043303	F	MP:0002175	decreased brain weight	Mecp2<tm1.1Jae>/Mecp2<+>	involves: 129S4/SvJae * C57BL/6	N	15069197
MGI:3043383	M	MP:0001922	reduced male fertility	Mmel1<tm1Ldg>/Mmel1<tm1Ldg>	involves: 129S/SvEv * MF1	N	15121861
MGI:3043383	M	MP:0001925	male infertility	Mmel1<tm1Ldg>/Mmel1<tm1Ldg>	involves: 129S/SvEv * MF1	N	15121861
MGI:3043388	M	MP:0004852	decreased testis weight	Tesq2<L6>/Tesq2<L6>	involves: L6 * M16i	N	15058381
MGI:3043393	M	MP:0004851	increased testis weight	Tesq3<L6>/Tesq3<L6>	involves: L6 * M16i	N	15058381
MGI:3043394	M	MP:0004851	increased testis weight	Tesq3<L6>/Tesq3<M16i>	involves: L6 * M16i	N	15058381
MGI:3043396	M	MP:0004852	decreased testis weight	Tesq1<L6>/Tesq1<L6>	involves: L6 * M16i	N	15058381
MGI:3043417	M	MP:0005389	reproductive system phenotype	Elk1<tm2Nor>/Y	involves: 129P2/OlaHsd * C57BL/6N	Y	14994271
MGI:3043418	F	MP:0005389	reproductive system phenotype	Elk1<tm2Nor>/Elk1<tm2Nor>	involves: 129P2/OlaHsd * C57BL/6N	Y	14994271
MGI:3043447	M	MP:0002717	abnormal male preputial gland morphology	Uaca<tm1Kiy>/Uaca<tm1Kiy>	involves: 129P2/OlaHsd	N	14961764
MGI:3043451	M	MP:0002717	abnormal male preputial gland morphology	Uaca<tm1Kiy>/Uaca<+>	involves: 129P2/OlaHsd	N	14961764
MGI:3043558	M	MP:0011169	abnormal white fat cell differentation	Ifrd1<tm1Lah>/Ifrd1<tm1Lah>	involves: 129P2/OlaHsd * C57BL/6	N	37603466
MGI:3043558	M	MP:0008853	decreased abdominal adipose tissue amount	Ifrd1<tm1Lah>/Ifrd1<tm1Lah>	involves: 129P2/OlaHsd * C57BL/6	N	37603466
MGI:3043585	M	MP:0008898	abnormal acrosome morphology	X/Del(Y)1Psb Sry<dl1Rlb>,Tg(Sry)2Ei/0	involves: 129S6/SvEvTac * MF1	N	15020475
MGI:3043585	M	MP:0001925	male infertility	X/Del(Y)1Psb Sry<dl1Rlb>,Tg(Sry)2Ei/0	involves: 129S6/SvEvTac * MF1	N	15020475
MGI:3043655	F	MP:0002169	no abnormal phenotype detected	Rhox5<tm1Clm>/Rhox5<tm1Clm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	9769172
MGI:3043693	F	MP:0001881	abnormal mammary gland physiology	Atp7b<tm1Tcg>/Atp7b<tm1Tcg>	involves: 129S1/Sv	N	10441329
MGI:3043880	M	MP:0020869	immotile sperm	Mlxipl<tm1Kuy>/Mlxipl<tm1Kuy>	involves: 129S6/SvEvTac * C57BL/6J	N	34669700
MGI:3043880	M	MP:0001925	male infertility	Mlxipl<tm1Kuy>/Mlxipl<tm1Kuy>	involves: 129S6/SvEvTac * C57BL/6J	N	34669700
MGI:3043880	M	MP:0002675	asthenozoospermia	Mlxipl<tm1Kuy>/Mlxipl<tm1Kuy>	involves: 129S6/SvEvTac * C57BL/6J	N	34669700
MGI:3043935	F	MP:0008000	increased ovary tumor incidence	Mutyh<tm1Jhmi>/Mutyh<tm1Jhmi>,Ogg1<tm1Tld>/Ogg1<tm1Tld>	involves: 129 * C57BL/6J	N	15126346
MGI:3043953	F	MP:0008000	increased ovary tumor incidence	Msh2<tm1Mak>/Msh2<+>,Mutyh<tm1Jhmi>/Mutyh<tm1Jhmi>,Ogg1<tm1Tld>/Ogg1<tm1Tld>	involves: 129 * C57BL/6J	N	15126346
MGI:3044184	F	MP:0001463	abnormal spatial learning	App<tm1Ini>/App<+>	involves: C57BL/6 * CBA * CD-1	N	15147316
MGI:3044184	M	MP:0001392	abnormal locomotor behavior	App<tm1Ini>/App<+>	involves: C57BL/6 * CBA * CD-1	N	15147316
MGI:3044184	M	MP:0031391	increased locomotor activity	App<tm1Ini>/App<+>	involves: C57BL/6 * CBA * CD-1	N	15147316
MGI:3044192	F	MP:0001926	female infertility	Cd9<tm1Kudo>/Cd9<tm1Kudo>	involves: 129X1/SvJ * C57BL/6N	N	10700183
MGI:3044232	F	MP:0002169	no abnormal phenotype detected	Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11930005
MGI:3044234	F	MP:0002169	no abnormal phenotype detected	Tfe3<tm1Est>/Tfe3<tm1Est>,Tfec<tm1Est>/Tfec<tm1Est>	either: (involves: 129/Sv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11930005
MGI:3044359	M	MP:0001156	abnormal spermatogenesis	Hsf1<tm1Anak>/Hsf1<tm1Anak>	involves: C57BL/6 * CBA * ICR	N	12954729
MGI:3044360	M	MP:0004852	decreased testis weight	Hsf1<tm1Anak>/Hsf1<tm1Anak>,Tg(ACTB-HSF1)1Anak/?	involves: C57BL/6 * CBA * ICR	N	12954729
MGI:3044360	M	MP:0002216	abnormal seminiferous tubule morphology	Hsf1<tm1Anak>/Hsf1<tm1Anak>,Tg(ACTB-HSF1)1Anak/?	involves: C57BL/6 * CBA * ICR	N	12954729
MGI:3044363	M	MP:0001145	abnormal male reproductive system morphology	Tg(ACTB-HSF1)1Anak/?	involves: C57BL/6 * CBA	N	10747023
MGI:3044363	M	MP:0001153	small seminiferous tubules	Tg(ACTB-HSF1)1Anak/?	involves: C57BL/6 * CBA	N	10747023
MGI:3044363	M	MP:0001925	male infertility	Tg(ACTB-HSF1)1Anak/?	involves: C57BL/6 * CBA	N	10747023
MGI:3044363	M	MP:0008261	arrest of male meiosis	Tg(ACTB-HSF1)1Anak/?	involves: C57BL/6 * CBA	N	10747023
MGI:3044363	M	MP:0004852	decreased testis weight	Tg(ACTB-HSF1)1Anak/?	involves: C57BL/6 * CBA	N	10747023
MGI:3044415	F	MP:0000067	osteopetrosis	Mitf<mi-vga9>/Mitf<mi-vga9>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6 * CBA) or (involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA)	N	11930005
MGI:3044415	F	MP:0004982	abnormal osteoclast morphology	Mitf<mi-vga9>/Mitf<mi-vga9>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6 * CBA) or (involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA)	N	11930005
MGI:3044415	F	MP:0011085	postnatal lethality, complete penetrance	Mitf<mi-vga9>/Mitf<mi-vga9>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6 * CBA) or (involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA)	N	11930005
MGI:3044415	F	MP:0003053	delayed tooth eruption	Mitf<mi-vga9>/Mitf<mi-vga9>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6 * CBA) or (involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA)	N	11930005
MGI:3044415	F	MP:0001297	microphthalmia	Mitf<mi-vga9>/Mitf<mi-vga9>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6 * CBA) or (involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA)	N	11930005
MGI:3044415	F	MP:0005171	absent coat pigmentation	Mitf<mi-vga9>/Mitf<mi-vga9>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6 * CBA) or (involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA)	N	11930005
MGI:3044416	F	MP:0004982	abnormal osteoclast morphology	Mitf<mi-ew>/Mitf<mi-ew>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6Bn * NAW) or (involves: 129S1/Sv * C57BL/6Bn * C57BL/6J * NAW)	N	11930005
MGI:3044416	F	MP:0001262	decreased body weight	Mitf<mi-ew>/Mitf<mi-ew>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6Bn * NAW) or (involves: 129S1/Sv * C57BL/6Bn * C57BL/6J * NAW)	N	11930005
MGI:3044416	F	MP:0005171	absent coat pigmentation	Mitf<mi-ew>/Mitf<mi-ew>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6Bn * NAW) or (involves: 129S1/Sv * C57BL/6Bn * C57BL/6J * NAW)	N	11930005
MGI:3044416	F	MP:0000067	osteopetrosis	Mitf<mi-ew>/Mitf<mi-ew>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6Bn * NAW) or (involves: 129S1/Sv * C57BL/6Bn * C57BL/6J * NAW)	N	11930005
MGI:3044416	F	MP:0011085	postnatal lethality, complete penetrance	Mitf<mi-ew>/Mitf<mi-ew>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6Bn * NAW) or (involves: 129S1/Sv * C57BL/6Bn * C57BL/6J * NAW)	N	11930005
MGI:3044416	F	MP:0001297	microphthalmia	Mitf<mi-ew>/Mitf<mi-ew>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6Bn * NAW) or (involves: 129S1/Sv * C57BL/6Bn * C57BL/6J * NAW)	N	11930005
MGI:3044416	F	MP:0003053	delayed tooth eruption	Mitf<mi-ew>/Mitf<mi-ew>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6Bn * NAW) or (involves: 129S1/Sv * C57BL/6Bn * C57BL/6J * NAW)	N	11930005
MGI:3044424	F	MP:0000067	osteopetrosis	Mitf<Mi-wh>/Mitf<Mi-wh>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL * DBA) or (involves: 129S1/Sv * C57BL * C57BL/6J * DBA)	N	11930005
MGI:3044424	F	MP:0001262	decreased body weight	Mitf<Mi-wh>/Mitf<Mi-wh>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL * DBA) or (involves: 129S1/Sv * C57BL * C57BL/6J * DBA)	N	11930005
MGI:3044424	F	MP:0001297	microphthalmia	Mitf<Mi-wh>/Mitf<Mi-wh>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL * DBA) or (involves: 129S1/Sv * C57BL * C57BL/6J * DBA)	N	11930005
MGI:3044424	F	MP:0005171	absent coat pigmentation	Mitf<Mi-wh>/Mitf<Mi-wh>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL * DBA) or (involves: 129S1/Sv * C57BL * C57BL/6J * DBA)	N	11930005
MGI:3044424	F	MP:0011086	postnatal lethality, incomplete penetrance	Mitf<Mi-wh>/Mitf<Mi-wh>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL * DBA) or (involves: 129S1/Sv * C57BL * C57BL/6J * DBA)	N	11930005
MGI:3044640	M	MP:0004851	increased testis weight	Tesw1<NZB/BlNJ>/Tesw1<NZB/BlNJ>	involves: C57BL/6By * NZB/BlNJ	N	11333241
MGI:3044641	M	MP:0004851	increased testis weight	Tesw2<NZB/BlNJ>/Tesw2<NZB/BlNJ>	involves: C57BL/6By * NZB/BlNJ	N	11333241
MGI:3044642	M	MP:0004909	increased seminal vesicle weight	Tsvw1<NZB/BlNJ>/Tsvw1<NZB/BlNJ>	involves: C57BL/6By * NZB/BlNJ	N	11333241
MGI:3044642	M	MP:0004851	increased testis weight	Tsvw1<NZB/BlNJ>/Tsvw1<NZB/BlNJ>	involves: C57BL/6By * NZB/BlNJ	N	11333241
MGI:3044667	F	MP:0001126	abnormal ovary morphology	Foxl2<tm1Gpil>/Foxl2<tm1Gpil>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6J) or (involves: 129S6/SvEvTac * NIHS-BC)	N	15056605
MGI:3044667	F	MP:0001926	female infertility	Foxl2<tm1Gpil>/Foxl2<tm1Gpil>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6J) or (involves: 129S6/SvEvTac * NIHS-BC)	N	15056605
MGI:3044667	F	MP:0001129	impaired ovarian folliculogenesis	Foxl2<tm1Gpil>/Foxl2<tm1Gpil>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6J) or (involves: 129S6/SvEvTac * NIHS-BC)	N	15056605
MGI:3044673	M	MP:0013600	testis degeneration	Hip1<tm3Tsr>/Hip1<tm3Tsr>	involves: 129X1/SvJ * C57BL/6	N	14998932
MGI:3044673	M	MP:0001922	reduced male fertility	Hip1<tm3Tsr>/Hip1<tm3Tsr>	involves: 129X1/SvJ * C57BL/6	N	14998932
MGI:3044673	M	MP:0006380	abnormal spermatid morphology	Hip1<tm3Tsr>/Hip1<tm3Tsr>	involves: 129X1/SvJ * C57BL/6	N	14998932
MGI:3044674	M	MP:0004852	decreased testis weight	Hip1<tm1Tsr>/Hip1<tm1Tsr>	involves: 129X1/SvJ * C57BL/6	N	11604514
MGI:3044674	M	MP:0002216	abnormal seminiferous tubule morphology	Hip1<tm1Tsr>/Hip1<tm1Tsr>	involves: 129X1/SvJ * C57BL/6	N	14998932
MGI:3044674	M	MP:0014052	increased male germ cell apoptosis	Hip1<tm1Tsr>/Hip1<tm1Tsr>	involves: 129X1/SvJ * C57BL/6	N	11604514
MGI:3044674	M	MP:0020550	multinucleated giant male germ cells	Hip1<tm1Tsr>/Hip1<tm1Tsr>	involves: 129X1/SvJ * C57BL/6	N	14998932
MGI:3044674	M	MP:0001156	abnormal spermatogenesis	Hip1<tm1Tsr>/Hip1<tm1Tsr>	involves: 129X1/SvJ * C57BL/6	N	11604514
MGI:3044674	M	MP:0002687	oligozoospermia	Hip1<tm1Tsr>/Hip1<tm1Tsr>	involves: 129X1/SvJ * C57BL/6	N	11604514
MGI:3044674	M	MP:0001154	seminiferous tubule degeneration	Hip1<tm1Tsr>/Hip1<tm1Tsr>	involves: 129X1/SvJ * C57BL/6	N	11604514
MGI:3044674	M	MP:0004901	decreased male germ cell number	Hip1<tm1Tsr>/Hip1<tm1Tsr>	involves: 129X1/SvJ * C57BL/6	N	11604514
MGI:3044674	M	MP:0003205	testicular atrophy	Hip1<tm1Tsr>/Hip1<tm1Tsr>	involves: 129X1/SvJ * C57BL/6	N	11604514
MGI:3044675	M	MP:0001925	male infertility	Hip1<tm2.1Tsr>/Hip1<tm2.1Tsr>	involves: 129X1/SvJ	N	14998932
MGI:3044676	M	MP:0001925	male infertility	Gamt<tm1Isb>/Gamt<tm1Isb>	involves: 129S1/Sv * 129X1/SvJ	N	15028668
MGI:3044676	M	MP:0020550	multinucleated giant male germ cells	Gamt<tm1Isb>/Gamt<tm1Isb>	involves: 129S1/Sv * 129X1/SvJ	N	15028668
MGI:3044676	M	MP:0001922	reduced male fertility	Gamt<tm1Isb>/Gamt<tm1Isb>	involves: 129S1/Sv * 129X1/SvJ	N	15028668
MGI:3044676	M	MP:0002216	abnormal seminiferous tubule morphology	Gamt<tm1Isb>/Gamt<tm1Isb>	involves: 129S1/Sv * 129X1/SvJ	N	15028668
MGI:3044676	M	MP:0002687	oligozoospermia	Gamt<tm1Isb>/Gamt<tm1Isb>	involves: 129S1/Sv * 129X1/SvJ	N	15028668
MGI:3044687	M	MP:0004910	decreased seminal vesicle weight	Ar<tm1Reb>/Y	involves: 129S4/SvJaeSor	N	14701682
MGI:3044687	M	MP:0001751	increased circulating luteinizing hormone level	Ar<tm1Reb>/Y	involves: 129S4/SvJaeSor	N	14701682
MGI:3044687	M	MP:0001750	increased circulating follicle stimulating hormone level	Ar<tm1Reb>/Y	involves: 129S4/SvJaeSor	N	14701682
MGI:3044687	M	MP:0005117	increased circulating pituitary hormone level	Ar<tm1Reb>/Y	involves: 129S4/SvJaeSor	N	14701682
MGI:3044687	M	MP:0004852	decreased testis weight	Ar<tm1Reb>/Y	involves: 129S4/SvJaeSor	N	14701682
MGI:3044687	M	MP:0002216	abnormal seminiferous tubule morphology	Ar<tm1Reb>/Y	involves: 129S4/SvJaeSor	N	14701682
MGI:3044687	M	MP:0002781	increased circulating testosterone level	Ar<tm1Reb>/Y	involves: 129S4/SvJaeSor	N	14701682
MGI:3044687	M	MP:0002687	oligozoospermia	Ar<tm1Reb>/Y	involves: 129S4/SvJaeSor	N	14701682
MGI:3044687	M	MP:0005386	behavior/neurological phenotype	Ar<tm1Reb>/Y	involves: 129S4/SvJaeSor	Y	14701682
MGI:3044687	M	MP:0001146	abnormal testis morphology	Ar<tm1Reb>/Y	involves: 129S4/SvJaeSor	N	14701682
MGI:3044688	M	MP:0001750	increased circulating follicle stimulating hormone level	Ar<tm1Reb>/Y,Tg(Amh-cre)8815Reb/?	involves: 129S4/SvJaeSor * FVB/N	N	14701682
MGI:3044688	M	MP:0005159	azoospermia	Ar<tm1Reb>/Y,Tg(Amh-cre)8815Reb/?	involves: 129S4/SvJaeSor * FVB/N	N	14701682
MGI:3044688	M	MP:0001751	increased circulating luteinizing hormone level	Ar<tm1Reb>/Y,Tg(Amh-cre)8815Reb/?	involves: 129S4/SvJaeSor * FVB/N	N	14701682
MGI:3044688	M	MP:0005117	increased circulating pituitary hormone level	Ar<tm1Reb>/Y,Tg(Amh-cre)8815Reb/?	involves: 129S4/SvJaeSor * FVB/N	N	14701682
MGI:3044688	M	MP:0004852	decreased testis weight	Ar<tm1Reb>/Y,Tg(Amh-cre)8815Reb/?	involves: 129S4/SvJaeSor * FVB/N	N	14701682
MGI:3044688	M	MP:0001146	abnormal testis morphology	Ar<tm1Reb>/Y,Tg(Amh-cre)8815Reb/?	involves: 129S4/SvJaeSor * FVB/N	N	14701682
MGI:3044688	M	MP:0002781	increased circulating testosterone level	Ar<tm1Reb>/Y,Tg(Amh-cre)8815Reb/?	involves: 129S4/SvJaeSor * FVB/N	N	14701682
MGI:3044688	M	MP:0002216	abnormal seminiferous tubule morphology	Ar<tm1Reb>/Y,Tg(Amh-cre)8815Reb/?	involves: 129S4/SvJaeSor * FVB/N	N	14701682
MGI:3044688	M	MP:0004910	decreased seminal vesicle weight	Ar<tm1Reb>/Y,Tg(Amh-cre)8815Reb/?	involves: 129S4/SvJaeSor * FVB/N	N	14701682
MGI:3044726	M	MP:0005449	abnormal food intake	Drd3<tm1Stl>/Drd3<tm1Stl>	involves: 129S2/SvPas * C57BL/6	N	15084447
MGI:3044726	M	MP:0001415	increased exploration in new environment	Drd3<tm1Stl>/Drd3<tm1Stl>	involves: 129S2/SvPas * C57BL/6	N	9354330
MGI:3044726	M	MP:0005455	increased susceptibility to weight gain	Drd3<tm1Stl>/Drd3<tm1Stl>	involves: 129S2/SvPas * C57BL/6	N	15084447
MGI:3044726	M	MP:0001454	abnormal cued conditioning behavior	Drd3<tm1Stl>/Drd3<tm1Stl>	involves: 129S2/SvPas * C57BL/6	N	9354330
MGI:3044726	F	MP:0005458	increased percent body fat/body weight	Drd3<tm1Stl>/Drd3<tm1Stl>	involves: 129S2/SvPas * C57BL/6	N	15084447
MGI:3044726	M	MP:0001399	hyperactivity	Drd3<tm1Stl>/Drd3<tm1Stl>	involves: 129S2/SvPas * C57BL/6	N	9354330
MGI:3044726	M	MP:0000676	abnormal body water content	Drd3<tm1Stl>/Drd3<tm1Stl>	involves: 129S2/SvPas * C57BL/6	N	15084447
MGI:3044888	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Cnot7<tm1Tno>/Cnot7<tm1Tno>	involves: 129S4/SvJae * C57BL/6J	N	15107851
MGI:3044888	M	MP:0014052	increased male germ cell apoptosis	Cnot7<tm1Tno>/Cnot7<tm1Tno>	involves: 129S4/SvJae * C57BL/6J	N	15107851
MGI:3044888	M	MP:0002687	oligozoospermia	Cnot7<tm1Tno>/Cnot7<tm1Tno>	involves: 129S4/SvJae * C57BL/6J	N	15107851
MGI:3044888	M	MP:0008892	abnormal sperm flagellum morphology	Cnot7<tm1Tno>/Cnot7<tm1Tno>	involves: 129S4/SvJae * C57BL/6J	N	15107851
MGI:3044888	M	MP:0001147	small testis	Cnot7<tm1Tno>/Cnot7<tm1Tno>	involves: 129S4/SvJae * C57BL/6J	N	15107851
MGI:3044888	M	MP:0009230	abnormal sperm head morphology	Cnot7<tm1Tno>/Cnot7<tm1Tno>	involves: 129S4/SvJae * C57BL/6J	N	15107851
MGI:3044888	M	MP:0005578	teratozoospermia	Cnot7<tm1Tno>/Cnot7<tm1Tno>	involves: 129S4/SvJae * C57BL/6J	N	15107851
MGI:3044888	M	MP:0020550	multinucleated giant male germ cells	Cnot7<tm1Tno>/Cnot7<tm1Tno>	involves: 129S4/SvJae * C57BL/6J	N	15107851
MGI:3044888	M	MP:0001925	male infertility	Cnot7<tm1Tno>/Cnot7<tm1Tno>	involves: 129S4/SvJae * C57BL/6J	N	15107851
MGI:3044888	M	MP:0002675	asthenozoospermia	Cnot7<tm1Tno>/Cnot7<tm1Tno>	involves: 129S4/SvJae * C57BL/6J	N	15107851
MGI:3044888	M	MP:0002784	abnormal Sertoli cell morphology	Cnot7<tm1Tno>/Cnot7<tm1Tno>	involves: 129S4/SvJae * C57BL/6J	N	15107851
MGI:3044888	M	MP:0006380	abnormal spermatid morphology	Cnot7<tm1Tno>/Cnot7<tm1Tno>	involves: 129S4/SvJae * C57BL/6J	N	15107851
MGI:3044888	M	MP:0001154	seminiferous tubule degeneration	Cnot7<tm1Tno>/Cnot7<tm1Tno>	involves: 129S4/SvJae * C57BL/6J	N	15107851
MGI:3044922	F	MP:0001385	pup cannibalization	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	N	7557388
MGI:3044922	F	MP:0006269	abnormal mammary gland growth during pregnancy	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	N	7557388
MGI:3044922	F	MP:0010249	lactation failure	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	N	7557388
MGI:3044922	F	MP:0006270	abnormal mammary gland growth during lactation	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	N	7557388
MGI:3044974	F	MP:0001926	female infertility	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129 * C57BL/6	N	11134518
MGI:3044974	F	MP:0002679	abnormal corpus luteum morphology	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129 * C57BL/6	N	11134518
MGI:3044974	M	MP:0001148	enlarged testis	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129 * C57BL/6	N	11134518
MGI:3044989	F	MP:0003009	abnormal cytokine secretion	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>,Tg(DO11.10)10Dlo/Tg(DO11.10)10Dlo	involves: BALB/c * C3H * C57BL/6	N	15123745
MGI:3044992	F	MP:0005026	decreased susceptibility to parasitic infection	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	involves: BALB/c	N	15123745
MGI:3045105	F	MP:0001129	impaired ovarian folliculogenesis	Kitl<Sl-pan>/Kitl<Sl-pan>	either: (involves: C3H/HeJ * C57BL/6J) or (involves: C3H/HeN * C57BL/6J)	N	7533739
MGI:3045105	F	MP:0001926	female infertility	Kitl<Sl-pan>/Kitl<Sl-pan>	either: (involves: C3H/HeJ * C57BL/6J) or (involves: C3H/HeN * C57BL/6J)	N	7533739
MGI:3045105	F	MP:0005431	decreased oocyte number	Kitl<Sl-pan>/Kitl<Sl-pan>	either: (involves: C3H/HeJ * C57BL/6J) or (involves: C3H/HeN * C57BL/6J)	N	7533739
MGI:3045114	F	MP:0005431	decreased oocyte number	Kitl<Sl-con>/Kitl<+>	either: (involves: C3H/HeJ) or (involves: C3H/HeN)	N	7533739
MGI:3045114	F	MP:0001130	abnormal ovarian folliculogenesis	Kitl<Sl-con>/Kitl<+>	either: (involves: C3H/HeJ) or (involves: C3H/HeN)	N	7533739
MGI:3045115	F	MP:0001129	impaired ovarian folliculogenesis	Kitl<Sl-con>/Kitl<Sl-con>	either: (involves: C3H/HeJ) or (involves: C3H/HeN)	N	7533739
MGI:3045115	F	MP:0005431	decreased oocyte number	Kitl<Sl-con>/Kitl<Sl-con>	either: (involves: C3H/HeJ) or (involves: C3H/HeN)	N	7533739
MGI:3045399	F	MP:0006269	abnormal mammary gland growth during pregnancy	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(MMTV-cre)1Mam/0	involves: 129X1/SvJ * C57BL/6 * FVB	N	15169911
MGI:3045399	F	MP:0010249	lactation failure	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(MMTV-cre)1Mam/0	involves: 129X1/SvJ * C57BL/6 * FVB	N	15169911
MGI:3045399	F	MP:0000628	abnormal mammary gland development	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(MMTV-cre)1Mam/0	involves: 129X1/SvJ * C57BL/6 * FVB	N	15169911
MGI:3045431	M	MP:0001155	arrest of spermatogenesis	Poc1a<cha>/Poc1a<cha>	involves: DBA/2J	N	15177549
MGI:3045431	M	MP:0001925	male infertility	Poc1a<cha>/Poc1a<cha>	involves: DBA/2J	N	15177549
MGI:3045431	M	MP:0005159	azoospermia	Poc1a<cha>/Poc1a<cha>	involves: DBA/2J	N	15177549
MGI:3045431	M	MP:0002216	abnormal seminiferous tubule morphology	Poc1a<cha>/Poc1a<cha>	involves: DBA/2J	N	15177549
MGI:3045511	F	MP:0001926	female infertility	Pcyt1b<tm1Mkar>/Pcyt1b<tm1Mkar>	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045511	F	MP:0002777	absent ovarian follicles	Pcyt1b<tm1Mkar>/Pcyt1b<tm1Mkar>	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045511	F	MP:0001751	increased circulating luteinizing hormone level	Pcyt1b<tm1Mkar>/Pcyt1b<tm1Mkar>	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045511	F	MP:0002020	increased tumor incidence	Pcyt1b<tm1Mkar>/Pcyt1b<tm1Mkar>	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045511	F	MP:0001750	increased circulating follicle stimulating hormone level	Pcyt1b<tm1Mkar>/Pcyt1b<tm1Mkar>	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045511	F	MP:0001134	absent corpus luteum	Pcyt1b<tm1Mkar>/Pcyt1b<tm1Mkar>	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045511	F	MP:0001128	ovary hyperplasia	Pcyt1b<tm1Mkar>/Pcyt1b<tm1Mkar>	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045511	F	MP:0001126	abnormal ovary morphology	Pcyt1b<tm1Mkar>/Pcyt1b<tm1Mkar>	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045521	F	MP:0001926	female infertility	Pcyt1b<tm1Mkar>/Pcyt1b<+>	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045521	F	MP:0001134	absent corpus luteum	Pcyt1b<tm1Mkar>/Pcyt1b<+>	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045521	F	MP:0002777	absent ovarian follicles	Pcyt1b<tm1Mkar>/Pcyt1b<+>	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045529	M	MP:0003205	testicular atrophy	Pcyt1b<tm1Mkar>/Y	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045529	M	MP:0001154	seminiferous tubule degeneration	Pcyt1b<tm1Mkar>/Y	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045529	M	MP:0001156	abnormal spermatogenesis	Pcyt1b<tm1Mkar>/Y	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045529	M	MP:0001922	reduced male fertility	Pcyt1b<tm1Mkar>/Y	involves: 129S1/Sv * C57BL/6J	N	15143167
MGI:3045535	F	MP:0004762	increased anti-double stranded DNA antibody level	Mfge8<tm1Osa>/Mfge8<tm1Osa>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23443560
MGI:3045535	F	MP:0001882	abnormal lactation	Mfge8<tm1Osa>/Mfge8<tm1Osa>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16275924
MGI:3045547	M	MP:0008545	absent sperm flagellum	Bbs4<tm1Vcs>/Bbs4<tm1Vcs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15173597
MGI:3045547	M	MP:0001925	male infertility	Bbs4<tm1Vcs>/Bbs4<tm1Vcs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15173597
MGI:3045624	M	MP:0001145	abnormal male reproductive system morphology	Smad1<tm2Sor>/Smad1<tm2Sor>	involves: 129S4/SvJaeSor * C57BL/6	N	15198985
MGI:3045624	M	MP:0006419	disorganized testis cords	Smad1<tm2Sor>/Smad1<tm2Sor>	involves: 129S4/SvJaeSor * C57BL/6	N	15198985
MGI:3045624	M	MP:0001147	small testis	Smad1<tm2Sor>/Smad1<tm2Sor>	involves: 129S4/SvJaeSor * C57BL/6	N	15198985
MGI:3045813	F	MP:0006269	abnormal mammary gland growth during pregnancy	Chuk<tm2Mka>/Chuk<tm2Mka>	Not Specified	N	11747812
MGI:3045813	F	MP:0009506	abnormal mammary gland alveolus morphology	Chuk<tm2Mka>/Chuk<tm2Mka>	Not Specified	N	11747812
MGI:3045813	F	MP:0001882	abnormal lactation	Chuk<tm2Mka>/Chuk<tm2Mka>	Not Specified	N	11747812
MGI:3045813	F	MP:0009504	abnormal mammary gland epithelium morphology	Chuk<tm2Mka>/Chuk<tm2Mka>	Not Specified	N	11747812
MGI:3045814	F	MP:0006270	abnormal mammary gland growth during lactation	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Wap-cre)11738Mam/0	involves: 129X1/SvJ * C57BL/6 * FVB	N	15169911
MGI:3045884	M	MP:0004852	decreased testis weight	Ddx25<tm1Mld>/Ddx25<tm1Mld>	involves: 129S4/SvJae	N	15096601
MGI:3045884	M	MP:0001156	abnormal spermatogenesis	Ddx25<tm1Mld>/Ddx25<tm1Mld>	involves: 129S4/SvJae	N	15096601
MGI:3045884	M	MP:0001925	male infertility	Ddx25<tm1Mld>/Ddx25<tm1Mld>	involves: 129S4/SvJae	N	15096601
MGI:3045884	M	MP:0001155	arrest of spermatogenesis	Ddx25<tm1Mld>/Ddx25<tm1Mld>	involves: 129S4/SvJae	N	15096601
MGI:3045884	M	MP:0014052	increased male germ cell apoptosis	Ddx25<tm1Mld>/Ddx25<tm1Mld>	involves: 129S4/SvJae	N	15096601
MGI:3045884	M	MP:0002786	abnormal Leydig cell morphology	Ddx25<tm1Mld>/Ddx25<tm1Mld>	involves: 129S4/SvJae	N	15096601
MGI:3045981	F	MP:0002016	ovary cyst	Rspo2<ftls>/Rspo2<+>	involves: FVB/N	N	12782276
MGI:3045981	F	MP:0003355	decreased ovulation rate	Rspo2<ftls>/Rspo2<+>	involves: FVB/N	N	12782276
MGI:3045981	F	MP:0001923	reduced female fertility	Rspo2<ftls>/Rspo2<+>	involves: FVB/N	N	12782276
MGI:3045986	F	MP:0004996	abnormal CNS synapse formation	Syn1<tm1Pggd>/Syn1<tm1Pggd>,Syn2<tm1Pggd>/Syn2<tm1Pggd>	involves: 129P2/OlaHsd	N	9513186
MGI:3045986	F	MP:0003631	nervous system phenotype	Syn1<tm1Pggd>/Syn1<tm1Pggd>,Syn2<tm1Pggd>/Syn2<tm1Pggd>	involves: 129P2/OlaHsd	Y	9513186
MGI:3046051	M	MP:0011801	urethra obstruction	Htr3a<tm1Ckn>/Htr3a<tm1Ckn>	involves: 129S1/Sv * C57BL/6J * DBA/2	N	15201326
MGI:3046051	M	MP:0009552	urinary bladder obstruction	Htr3a<tm1Ckn>/Htr3a<tm1Ckn>	involves: 129S1/Sv * C57BL/6J * DBA/2	N	15201326
MGI:3046051	M	MP:0011784	abnormal urinary bladder neck morphology	Htr3a<tm1Ckn>/Htr3a<tm1Ckn>	involves: 129S1/Sv * C57BL/6J * DBA/2	N	15201326
MGI:3046051	M	MP:0011777	abnormal male prostatic urethra morphology	Htr3a<tm1Ckn>/Htr3a<tm1Ckn>	involves: 129S1/Sv * C57BL/6J * DBA/2	N	15201326
MGI:3046051	M	MP:0003608	prostate gland inflammation	Htr3a<tm1Ckn>/Htr3a<tm1Ckn>	involves: 129S1/Sv * C57BL/6J * DBA/2	N	15201326
MGI:3046051	M	MP:0011802	seminal vesiculitis	Htr3a<tm1Ckn>/Htr3a<tm1Ckn>	involves: 129S1/Sv * C57BL/6J * DBA/2	N	15201326
MGI:3046056	M	MP:0008585	absent photoreceptor outer segment	Rs1<tm1Web>/Y	involves: 129S1/Sv * C57BL/6	N	11983912
MGI:3046056	M	MP:0008512	disorganized retina inner nuclear layer	Rs1<tm1Web>/Y	involves: 129S1/Sv * C57BL/6	N	11983912
MGI:3046056	M	MP:0008516	disorganized retina outer nuclear layer	Rs1<tm1Web>/Y	involves: 129S1/Sv * C57BL/6	N	11983912
MGI:3046056	M	MP:0004022	abnormal cone electrophysiology	Rs1<tm1Web>/Y	involves: 129S1/Sv * C57BL/6	N	11983912
MGI:3046056	M	MP:0003728	abnormal retina photoreceptor layer morphology	Rs1<tm1Web>/Y	involves: 129S1/Sv * C57BL/6	N	11983912
MGI:3046056	M	MP:0001325	abnormal retina morphology	Rs1<tm1Web>/Y	involves: 129S1/Sv * C57BL/6	N	11983912
MGI:3046056	M	MP:0005551	abnormal eye electrophysiology	Rs1<tm1Web>/Y	involves: 129S1/Sv * C57BL/6	N	11983912
MGI:3046056	M	MP:0008446	decreased retina cone cell number	Rs1<tm1Web>/Y	involves: 129S1/Sv * C57BL/6	N	11983912
MGI:3046061	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Nkx3-1<tm1.1Saa>/Nkx3-1<tm1.1Saa>	involves: 129S4/SvJaeSor * C57BL/6 * FVB/N	N	15111307
MGI:3046062	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Nkx3-1<tm1Saa>/Nkx3-1<tm1Saa>,Tg(KLK3-cre)13Saa/?	involves: C57BL/6	N	11839815
MGI:3046172	M	MP:0000031	abnormal cochlea morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0004740	sensorineural hearing loss	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15574296
MGI:3046172	M	MP:0000037	abnormal lateral semicircular canal morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0004739	conductive hearing loss	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15574296
MGI:3046172	M	MP:0001406	abnormal gait	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0004286	abnormal internal auditory canal morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0004290	abnormal stapes footplate morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15574296
MGI:3046172	M	MP:0001410	head bobbing	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0003148	decreased cochlea coiling	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0003167	abnormal scala tympani morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0001967	deafness	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0006025	distended Reissner membrane	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0011967	increased or absent threshold for auditory brainstem response	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15574296
MGI:3046172	M	MP:0001485	abnormal pinna reflex	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0004479	abnormal oval window morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15574296
MGI:3046172	M	MP:0005107	abnormal stapes morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15574296
MGI:3046172	M	MP:0005107	abnormal stapes morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0006012	dilated endolymphatic duct	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0006021	abnormal Reissner membrane morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0001282	short vibrissae	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0004411	decreased endocochlear potential	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15574296
MGI:3046172	M	MP:0005272	abnormal temporal bone morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0004287	abnormal spiral limbus morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0004862	small scala tympani	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0030407	abnormal stapes crus morpholgy	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15574296
MGI:3046172	M	MP:0003069	abnormal superior semicircular canal morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0003069	abnormal superior semicircular canal morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15655183
MGI:3046172	M	MP:0004289	abnormal bony labyrinth	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0009822	abnormal subarcuate fossa morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0004290	abnormal stapes footplate morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046172	M	MP:0004292	abnormal spiral ligament fibrocyte morphology	Pou3f4<tm1Cren>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10407036
MGI:3046176	M	MP:0002675	asthenozoospermia	Rxrb<tm1Ipc>/Rxrb<tm1Ipc>	involves: 129S2/SvPas	N	8557197
MGI:3046176	M	MP:0002216	abnormal seminiferous tubule morphology	Rxrb<tm1Ipc>/Rxrb<tm1Ipc>	involves: 129S2/SvPas	N	8557197
MGI:3046176	M	MP:0009238	coiled sperm flagellum	Rxrb<tm1Ipc>/Rxrb<tm1Ipc>	involves: 129S2/SvPas	N	8557197
MGI:3046176	M	MP:0008839	absent acrosome	Rxrb<tm1Ipc>/Rxrb<tm1Ipc>	involves: 129S2/SvPas	N	8557197
MGI:3046176	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Rxrb<tm1Ipc>/Rxrb<tm1Ipc>	involves: 129S2/SvPas	N	8557197
MGI:3046176	M	MP:0001925	male infertility	Rxrb<tm1Ipc>/Rxrb<tm1Ipc>	involves: 129S2/SvPas	N	8557197
MGI:3046176	M	MP:0002687	oligozoospermia	Rxrb<tm1Ipc>/Rxrb<tm1Ipc>	involves: 129S2/SvPas	N	8557197
MGI:3046176	M	MP:0008898	abnormal acrosome morphology	Rxrb<tm1Ipc>/Rxrb<tm1Ipc>	involves: 129S2/SvPas	N	8557197
MGI:3046176	M	MP:0001154	seminiferous tubule degeneration	Rxrb<tm1Ipc>/Rxrb<tm1Ipc>	involves: 129S2/SvPas	N	8557197
MGI:3046176	M	MP:0005578	teratozoospermia	Rxrb<tm1Ipc>/Rxrb<tm1Ipc>	involves: 129S2/SvPas	N	8557197
MGI:3046176	M	MP:0001155	arrest of spermatogenesis	Rxrb<tm1Ipc>/Rxrb<tm1Ipc>	involves: 129S2/SvPas	N	8557197
MGI:3046176	M	MP:0009231	detached acrosome	Rxrb<tm1Ipc>/Rxrb<tm1Ipc>	involves: 129S2/SvPas	N	8557197
MGI:3046295	F	MP:0005659	decreased susceptibility to diet-induced obesity	Fabp2<tm1Mto>/Fabp2<tm1Mto>	B6.129S1-Fabp2<tm1Mto>	N	11023988
MGI:3046295	M	MP:0003443	increased circulating glycerol level	Fabp2<tm1Mto>/Fabp2<tm1Mto>	B6.129S1-Fabp2<tm1Mto>	N	11023988
MGI:3046295	F	MP:0003402	decreased liver weight	Fabp2<tm1Mto>/Fabp2<tm1Mto>	B6.129S1-Fabp2<tm1Mto>	N	11023988
MGI:3046295	M	MP:0005669	increased circulating leptin level	Fabp2<tm1Mto>/Fabp2<tm1Mto>	B6.129S1-Fabp2<tm1Mto>	N	11023988
MGI:3046295	F	MP:0009307	decreased uterine fat pad weight	Fabp2<tm1Mto>/Fabp2<tm1Mto>	B6.129S1-Fabp2<tm1Mto>	N	11023988
MGI:3046295	M	MP:0003917	increased kidney weight	Fabp2<tm1Mto>/Fabp2<tm1Mto>	B6.129S1-Fabp2<tm1Mto>	N	11023988
MGI:3046295	F	MP:0005179	decreased circulating cholesterol level	Fabp2<tm1Mto>/Fabp2<tm1Mto>	B6.129S1-Fabp2<tm1Mto>	N	11023988
MGI:3046295	M	MP:0009288	increased epididymal fat pad weight	Fabp2<tm1Mto>/Fabp2<tm1Mto>	B6.129S1-Fabp2<tm1Mto>	N	11023988
MGI:3046295	M	MP:0002981	increased liver weight	Fabp2<tm1Mto>/Fabp2<tm1Mto>	B6.129S1-Fabp2<tm1Mto>	N	11023988
MGI:3046295	M	MP:0005658	increased susceptibility to diet-induced obesity	Fabp2<tm1Mto>/Fabp2<tm1Mto>	B6.129S1-Fabp2<tm1Mto>	N	11023988
MGI:3046465	F	MP:0001926	female infertility	Ncoa6<tm1Hhs>/Ncoa6<+>	129S6/SvEvTac-Ncoa6<tm1Hhs>	N	15143190
MGI:3046465	M	MP:0001922	reduced male fertility	Ncoa6<tm1Hhs>/Ncoa6<+>	129S6/SvEvTac-Ncoa6<tm1Hhs>	N	15143190
MGI:3046465	F	MP:0001923	reduced female fertility	Ncoa6<tm1Hhs>/Ncoa6<+>	129S6/SvEvTac-Ncoa6<tm1Hhs>	N	15143190
MGI:3046468	M	MP:0000031	abnormal cochlea morphology	Pou3f4<tm1Tno>/Y	involves: 129S4/SvJae * C57BL/6	N	10464101
MGI:3046468	M	MP:0005386	behavior/neurological phenotype	Pou3f4<tm1Tno>/Y	involves: 129S4/SvJae * C57BL/6	Y	10464101
MGI:3046468	M	MP:0004293	abnormal type I spiral ligament fibrocytes	Pou3f4<tm1Tno>/Y	involves: 129S4/SvJae * C57BL/6	N	10464101
MGI:3046468	M	MP:0004294	abnormal type II spiral ligament fibrocytes	Pou3f4<tm1Tno>/Y	involves: 129S4/SvJae * C57BL/6	N	10464101
MGI:3046468	M	MP:0004411	decreased endocochlear potential	Pou3f4<tm1Tno>/Y	involves: 129S4/SvJae * C57BL/6	N	10464101
MGI:3046468	M	MP:0011967	increased or absent threshold for auditory brainstem response	Pou3f4<tm1Tno>/Y	involves: 129S4/SvJae * C57BL/6	N	10464101
MGI:3046468	M	MP:0001967	deafness	Pou3f4<tm1Tno>/Y	involves: 129S4/SvJae * C57BL/6	N	10464101
MGI:3046505	F	MP:0001265	decreased body size	gro53/gro53	Not Specified	N	MGI:3038367
MGI:3046533	M	MP:0005367	renal/urinary system phenotype	Clcn5<tm1Tjj>/Y	B6.129-Clcn5<tm1Tjj>	Y	11099045
MGI:3046533	M	MP:0002901	increased urine phosphate level	Clcn5<tm1Tjj>/Y	B6.129-Clcn5<tm1Tjj>	N	11099045
MGI:3046533	M	MP:0002962	increased urine protein level	Clcn5<tm1Tjj>/Y	B6.129-Clcn5<tm1Tjj>	N	11099045
MGI:3046533	M	MP:0011417	abnormal renal transport	Clcn5<tm1Tjj>/Y	B6.129-Clcn5<tm1Tjj>	N	12548389
MGI:3046533	M	MP:0009350	decreased urine pH	Clcn5<tm1Tjj>/Y	B6.129-Clcn5<tm1Tjj>	N	11099045
MGI:3046533	M	MP:0005266	abnormal metabolism	Clcn5<tm1Tjj>/Y	B6.129-Clcn5<tm1Tjj>	N	12548389
MGI:3046533	M	MP:0011417	abnormal renal transport	Clcn5<tm1Tjj>/Y	B6.129-Clcn5<tm1Tjj>	N	11099045
MGI:3046533	M	MP:0001762	polyuria	Clcn5<tm1Tjj>/Y	B6.129-Clcn5<tm1Tjj>	N	11099045
MGI:3046533	M	MP:0011556	increased urine beta2-microglobulin level	Clcn5<tm1Tjj>/Y	B6.129-Clcn5<tm1Tjj>	N	11099045
MGI:3046533	M	MP:0005370	liver/biliary system phenotype	Clcn5<tm1Tjj>/Y	B6.129-Clcn5<tm1Tjj>	Y	11099045
MGI:3046582	M	MP:0001925	male infertility	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	N	15208629
MGI:3046582	M	MP:0002687	oligozoospermia	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	N	15208629
MGI:3046582	F	MP:0001926	female infertility	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	N	15208629
MGI:3046679	M	MP:0001147	small testis	Tg(CAG-DT)3Osb/0,Tg(Prm1-cre)1Osb/0	involves: C57BL * DBA	N	15358172
MGI:3046679	M	MP:0005159	azoospermia	Tg(CAG-DT)3Osb/0,Tg(Prm1-cre)1Osb/0	involves: C57BL * DBA	N	15358172
MGI:3046696	F	MP:0001882	abnormal lactation	Chek1<tm1Jmr>/Chek1<tm1Jmr>,Tg(Wap-cre)11738Mam/0	involves: C57BL/6	N	15261141
MGI:3046696	F	MP:0006269	abnormal mammary gland growth during pregnancy	Chek1<tm1Jmr>/Chek1<tm1Jmr>,Tg(Wap-cre)11738Mam/0	involves: C57BL/6	N	15261141
MGI:3046784	F	MP:0001385	pup cannibalization	Tfap2a<tm1Jae>/Tfap2a<+>	involves: 129P/Ola * 129S4/SvJae	N	11967920
MGI:3046848	M	MP:0001154	seminiferous tubule degeneration	Polg<tm1.1Lrsn>/Polg<tm1.1Lrsn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15164064
MGI:3046848	M	MP:0002687	oligozoospermia	Polg<tm1.1Lrsn>/Polg<tm1.1Lrsn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15164064
MGI:3046848	M	MP:0001922	reduced male fertility	Polg<tm1.1Lrsn>/Polg<tm1.1Lrsn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15164064
MGI:3046848	M	MP:0005159	azoospermia	Polg<tm1.1Lrsn>/Polg<tm1.1Lrsn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15164064
MGI:3046848	F	MP:0001923	reduced female fertility	Polg<tm1.1Lrsn>/Polg<tm1.1Lrsn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15164064
MGI:3046848	M	MP:0001147	small testis	Polg<tm1.1Lrsn>/Polg<tm1.1Lrsn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15164064
MGI:3046855	F	MP:0002293	long gestation period	Alppl2<tm1Jlm>/Alppl2<tm1Jlm>	129P3.Cg-Alppl2<tm1Jlm>	N	10767088
MGI:3046931	M	MP:0001147	small testis	Fxr1<tm1Dln>/Fxr1<tm1Dln>	involves: 129P2/OlaHsd * C57BL/6	N	15128702
MGI:3047099	F	MP:0001923	reduced female fertility	Fanca<tm1.1Wong>/Fanca<tm1.1Wong>	involves: C57BL/6	N	12913077
MGI:3047099	M	MP:0004852	decreased testis weight	Fanca<tm1.1Wong>/Fanca<tm1.1Wong>	involves: C57BL/6	N	12913077
MGI:3047099	M	MP:0001154	seminiferous tubule degeneration	Fanca<tm1.1Wong>/Fanca<tm1.1Wong>	involves: C57BL/6	N	12913077
MGI:3047101	M	MP:0001154	seminiferous tubule degeneration	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * CD-1)	N	12913077
MGI:3047126	M	MP:0001147	small testis	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	N	12913077
MGI:3047126	M	MP:0005169	abnormal male meiosis	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	N	12913077
MGI:3047126	F	MP:0001923	reduced female fertility	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	N	12913077
MGI:3047126	M	MP:0014052	increased male germ cell apoptosis	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	N	12913077
MGI:3047126	M	MP:0001156	abnormal spermatogenesis	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	N	12913077
MGI:3047126	M	MP:0001154	seminiferous tubule degeneration	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	N	12913077
MGI:3047131	M	MP:0001147	small testis	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: C57BL/6	N	12913077
MGI:3047139	F	MP:0004834	ovary hemorrhage	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or C57BL/6	N	12913077
MGI:3047139	F	MP:0001126	abnormal ovary morphology	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or C57BL/6	N	12913077
MGI:3047139	F	MP:0001127	small ovary	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or C57BL/6	N	12913077
MGI:3047139	F	MP:0002016	ovary cyst	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or C57BL/6	N	12913077
MGI:3047139	F	MP:0005158	ovary hypoplasia	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or C57BL/6	N	12913077
MGI:3047139	F	MP:0002682	decreased mature ovarian follicle number	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or C57BL/6	N	12913077
MGI:3047259	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Hprt1<tm1(UAS-Bmp4)Bhr>/Hprt1<+>,Tg(Wnt1-GAL4)1Rth/0	involves: 129S7/SvEvBrd * C57BL/6	N	15218525
MGI:3047259	F	MP:0000914	exencephaly	Hprt1<tm1(UAS-Bmp4)Bhr>/Hprt1<+>,Tg(Wnt1-GAL4)1Rth/0	involves: 129S7/SvEvBrd * C57BL/6	N	15218525
MGI:3047259	F	MP:0003984	embryonic growth retardation	Hprt1<tm1(UAS-Bmp4)Bhr>/Hprt1<+>,Tg(Wnt1-GAL4)1Rth/0	involves: 129S7/SvEvBrd * C57BL/6	N	15218525
MGI:3047259	F	MP:0001914	hemorrhage	Hprt1<tm1(UAS-Bmp4)Bhr>/Hprt1<+>,Tg(Wnt1-GAL4)1Rth/0	involves: 129S7/SvEvBrd * C57BL/6	N	15218525
MGI:3047260	F	MP:0002092	abnormal eye morphology	Hprt1<tm2(UAS-Bmp4)Bhr>/Hprt1<+>,Tg(Wnt1-GAL4)1Rth/0	involves: 129S7/SvEvBrd * C57BL/6	N	15218525
MGI:3047260	F	MP:0001914	hemorrhage	Hprt1<tm2(UAS-Bmp4)Bhr>/Hprt1<+>,Tg(Wnt1-GAL4)1Rth/0	involves: 129S7/SvEvBrd * C57BL/6	N	15218525
MGI:3047260	F	MP:0003984	embryonic growth retardation	Hprt1<tm2(UAS-Bmp4)Bhr>/Hprt1<+>,Tg(Wnt1-GAL4)1Rth/0	involves: 129S7/SvEvBrd * C57BL/6	N	15218525
MGI:3047260	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Hprt1<tm2(UAS-Bmp4)Bhr>/Hprt1<+>,Tg(Wnt1-GAL4)1Rth/0	involves: 129S7/SvEvBrd * C57BL/6	N	15218525
MGI:3047260	F	MP:0001614	abnormal blood vessel morphology	Hprt1<tm2(UAS-Bmp4)Bhr>/Hprt1<+>,Tg(Wnt1-GAL4)1Rth/0	involves: 129S7/SvEvBrd * C57BL/6	N	15218525
MGI:3047260	F	MP:0000914	exencephaly	Hprt1<tm2(UAS-Bmp4)Bhr>/Hprt1<+>,Tg(Wnt1-GAL4)1Rth/0	involves: 129S7/SvEvBrd * C57BL/6	N	15218525
MGI:3047562	M	MP:0002675	asthenozoospermia	Prnd<tm1Aag>/Prnd<tm1Aag>	involves: 129P2/OlaHsd	N	12110578
MGI:3047562	M	MP:0001925	male infertility	Prnd<tm1Aag>/Prnd<tm1Aag>	involves: 129P2/OlaHsd	N	12110578
MGI:3047562	M	MP:0002687	oligozoospermia	Prnd<tm1Aag>/Prnd<tm1Aag>	involves: 129P2/OlaHsd	N	12110578
MGI:3047562	M	MP:0030976	impaired sperm penetration of zona pellucida	Prnd<tm1Aag>/Prnd<tm1Aag>	involves: 129P2/OlaHsd	N	12110578
MGI:3047562	M	MP:0001932	abnormal spermiogenesis	Prnd<tm1Aag>/Prnd<tm1Aag>	involves: 129P2/OlaHsd	N	12110578
MGI:3047562	M	MP:0005578	teratozoospermia	Prnd<tm1Aag>/Prnd<tm1Aag>	involves: 129P2/OlaHsd	N	12110578
MGI:3047562	M	MP:0009230	abnormal sperm head morphology	Prnd<tm1Aag>/Prnd<tm1Aag>	involves: 129P2/OlaHsd	N	12110578
MGI:3047562	M	MP:0008898	abnormal acrosome morphology	Prnd<tm1Aag>/Prnd<tm1Aag>	involves: 129P2/OlaHsd	N	12110578
MGI:3047562	M	MP:0009243	hairpin sperm flagellum	Prnd<tm1Aag>/Prnd<tm1Aag>	involves: 129P2/OlaHsd	N	12110578
MGI:3047563	M	MP:0004542	impaired acrosome reaction	Prnd<tm1Dwm>/Prnd<tm1Dwm>	129P2/OlaHsd-Prnd<tm1Dwm>	N	15161660
MGI:3047563	M	MP:0001925	male infertility	Prnd<tm1Dwm>/Prnd<tm1Dwm>	129P2/OlaHsd-Prnd<tm1Dwm>	N	15161660
MGI:3047563	M	MP:0000242	impaired fertilization	Prnd<tm1Dwm>/Prnd<tm1Dwm>	129P2/OlaHsd-Prnd<tm1Dwm>	N	15161660
MGI:3047565	M	MP:0004542	impaired acrosome reaction	Prnp/Prnd<tm1Dwm>/Prnp/Prnd<tm1Dwm>	129P2/OlaHsd-Prnp/Prnd<tm1Dwm>	N	15161660
MGI:3047565	M	MP:0001925	male infertility	Prnp/Prnd<tm1Dwm>/Prnp/Prnd<tm1Dwm>	129P2/OlaHsd-Prnp/Prnd<tm1Dwm>	N	15161660
MGI:3047565	M	MP:0000242	impaired fertilization	Prnp/Prnd<tm1Dwm>/Prnp/Prnd<tm1Dwm>	129P2/OlaHsd-Prnp/Prnd<tm1Dwm>	N	15161660
MGI:3047566	M	MP:0001925	male infertility	Prnp/Prnd<tm1Dwm>/Prnp/Prnd<tm1Dwm>	129P2/OlaHsd-Prnp/Prnd<tm1Dwm>	N	15161660
MGI:3047566	M	MP:0000242	impaired fertilization	Prnp/Prnd<tm1Dwm>/Prnp/Prnd<tm1Dwm>	129P2/OlaHsd-Prnp/Prnd<tm1Dwm>	N	15161660
MGI:3047566	M	MP:0004542	impaired acrosome reaction	Prnp/Prnd<tm1Dwm>/Prnp/Prnd<tm1Dwm>	129P2/OlaHsd-Prnp/Prnd<tm1Dwm>	N	15161660
MGI:3047645	M	MP:0005578	teratozoospermia	Prnp/Prnd<tm1Aag>/Prnp/Prnd<tm1Aag>	Not Specified	N	15007175
MGI:3047645	M	MP:0001925	male infertility	Prnp/Prnd<tm1Aag>/Prnp/Prnd<tm1Aag>	Not Specified	N	15007175
MGI:3047648	M	MP:0005578	teratozoospermia	Prnp/Prnd<tm1Aag>/Prnp/Prnd<tm1Aag>	Not Specified	N	15007175
MGI:3047648	M	MP:0001925	male infertility	Prnp/Prnd<tm1Aag>/Prnp/Prnd<tm1Aag>	Not Specified	N	15007175
MGI:3047777	F	MP:0001762	polyuria	Avpr2<tm1Jwe>/Avpr2<+>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11104789
MGI:3047777	F	MP:0002136	abnormal kidney physiology	Avpr2<tm1Jwe>/Avpr2<+>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11104789
MGI:3047777	F	MP:0001426	polydipsia	Avpr2<tm1Jwe>/Avpr2<+>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11104789
MGI:3047777	F	MP:0002988	decreased urine osmolality	Avpr2<tm1Jwe>/Avpr2<+>	involves: 129S1/Sv * 129X1/SvJ * CF-1	N	11104789
MGI:3047840	M	MP:0001925	male infertility	Alpl<tm1(cre)Nagy>/Alpl<+>,Dnmt3a<tm3.1Enl>/Dnmt3a<tm3.2Enl>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	15215868
MGI:3047840	M	MP:0004852	decreased testis weight	Alpl<tm1(cre)Nagy>/Alpl<+>,Dnmt3a<tm3.1Enl>/Dnmt3a<tm3.2Enl>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	15215868
MGI:3047840	F	MP:0001926	female infertility	Alpl<tm1(cre)Nagy>/Alpl<+>,Dnmt3a<tm3.1Enl>/Dnmt3a<tm3.2Enl>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	15215868
MGI:3047840	M	MP:0005159	azoospermia	Alpl<tm1(cre)Nagy>/Alpl<+>,Dnmt3a<tm3.1Enl>/Dnmt3a<tm3.2Enl>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	15215868
MGI:3050153	F	MP:0001926	female infertility	Pde3a<tm1Vman>/Pde3a<tm1Vman>	either: (involves: 129X1/SvJ * C57BL/6J) or (involves: 129X1/SvJ * Black Swiss * C57BL/6J)	N	15254586
MGI:3050153	F	MP:0005168	abnormal female meiosis	Pde3a<tm1Vman>/Pde3a<tm1Vman>	either: (involves: 129X1/SvJ * C57BL/6J) or (involves: 129X1/SvJ * Black Swiss * C57BL/6J)	N	15254586
MGI:3050192	M	MP:0001265	decreased body size	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	11978731
MGI:3050192	M	MP:0002932	abnormal joint morphology	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	11978731
MGI:3050192	M	MP:0005503	abnormal tendon morphology	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	11978731
MGI:3050192	M	MP:0001406	abnormal gait	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	11978731
MGI:3050192	M	MP:0008271	abnormal bone ossification	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	11978731
MGI:3050192	M	MP:0003098	decreased tendon stiffness	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	11978731
MGI:3050192	M	MP:0011643	abnormal tendon collagen fibril morphology	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	11978731
MGI:3050192	M	MP:0003560	osteoarthritis	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	11978731
MGI:3050226	M	MP:0004215	abnormal myocardial fiber physiology	Hprt1<tm1Dhm>/Y	involves: 129P2/OlaHsd	N	16461894
MGI:3050226	M	MP:0005598	decreased heart ventricle muscle contractility	Hprt1<tm1Dhm>/Y	involves: 129P2/OlaHsd	N	15201433
MGI:3050226	M	MP:0001625	cardiac hypertrophy	Hprt1<tm1Dhm>/Y	involves: 129P2/OlaHsd	N	16461894
MGI:3050226	M	MP:0002833	increased heart weight	Hprt1<tm1Dhm>/Y	involves: 129P2/OlaHsd	N	15201433
MGI:3050226	M	MP:0005140	decreased cardiac muscle contractility	Hprt1<tm1Dhm>/Y	involves: 129P2/OlaHsd	N	16461894
MGI:3050226	M	MP:0004084	abnormal cardiac muscle relaxation	Hprt1<tm1Dhm>/Y	involves: 129P2/OlaHsd	N	16461894
MGI:3050227	F	MP:0004215	abnormal myocardial fiber physiology	Hprt1<tm1Dhm>/Hprt1<tm1Dhm>	involves: 129P2/OlaHsd	N	16461894
MGI:3050227	F	MP:0004084	abnormal cardiac muscle relaxation	Hprt1<tm1Dhm>/Hprt1<tm1Dhm>	involves: 129P2/OlaHsd	N	16461894
MGI:3050227	F	MP:0001625	cardiac hypertrophy	Hprt1<tm1Dhm>/Hprt1<tm1Dhm>	involves: 129P2/OlaHsd	N	16461894
MGI:3050227	F	MP:0002833	increased heart weight	Hprt1<tm1Dhm>/Hprt1<tm1Dhm>	involves: 129P2/OlaHsd	N	15201433
MGI:3050227	F	MP:0005598	decreased heart ventricle muscle contractility	Hprt1<tm1Dhm>/Hprt1<tm1Dhm>	involves: 129P2/OlaHsd	N	15201433
MGI:3050227	F	MP:0005140	decreased cardiac muscle contractility	Hprt1<tm1Dhm>/Hprt1<tm1Dhm>	involves: 129P2/OlaHsd	N	16461894
MGI:3050246	F	MP:0001923	reduced female fertility	Nr5a2<tm1Bel>/Nr5a2<+>	involves: 129/Sv * C57BL/6 * SJL	N	17409375
MGI:3050246	F	MP:0004904	increased uterus weight	Nr5a2<tm1Bel>/Nr5a2<+>	involves: 129/Sv * C57BL/6 * SJL	N	17409375
MGI:3050246	F	MP:0009661	abnormal pregnancy	Nr5a2<tm1Bel>/Nr5a2<+>	involves: 129/Sv * C57BL/6 * SJL	N	17409375
MGI:3050508	F	MP:0031020	premature ovarian failure	Kif18a<gcd2>/Kif18a<gcd2>	involves: 129S1/Sv * C57BL/6	N	16822657
MGI:3050508	F	MP:0001126	abnormal ovary morphology	Kif18a<gcd2>/Kif18a<gcd2>	involves: 129S1/Sv * C57BL/6	N	16822657
MGI:3050508	F	MP:0005431	decreased oocyte number	Kif18a<gcd2>/Kif18a<gcd2>	involves: 129S1/Sv * C57BL/6	N	16822657
MGI:3050508	F	MP:0008871	abnormal ovarian follicle number	Kif18a<gcd2>/Kif18a<gcd2>	involves: 129S1/Sv * C57BL/6	N	16822657
MGI:3050508	M	MP:0001156	abnormal spermatogenesis	Kif18a<gcd2>/Kif18a<gcd2>	involves: 129S1/Sv * C57BL/6	N	12855593
MGI:3050508	M	MP:0001156	abnormal spermatogenesis	Kif18a<gcd2>/Kif18a<gcd2>	involves: 129S1/Sv * C57BL/6	N	16822657
MGI:3050508	M	MP:0004901	decreased male germ cell number	Kif18a<gcd2>/Kif18a<gcd2>	involves: 129S1/Sv * C57BL/6	N	16822657
MGI:3050508	F	MP:0001127	small ovary	Kif18a<gcd2>/Kif18a<gcd2>	involves: 129S1/Sv * C57BL/6	N	16822657
MGI:3050512	F	MP:0001926	female infertility	mei11b/mei11b	involves: C3HeB/FeJ * C57BL/6	N	12855593
MGI:3050512	F	MP:0005168	abnormal female meiosis	mei11b/mei11b	involves: C3HeB/FeJ * C57BL/6	N	12855593
MGI:3050530	M	MP:0001925	male infertility	mei7/mei7	involves: C3HeB/FeJ * C57BL/6	N	12855593
MGI:3050530	M	MP:0001156	abnormal spermatogenesis	mei7/mei7	involves: C3HeB/FeJ * C57BL/6	N	12855593
MGI:3050530	M	MP:0008261	arrest of male meiosis	mei7/mei7	involves: C3HeB/FeJ * C57BL/6	N	12855593
MGI:3050574	M	MP:0001146	abnormal testis morphology	Akap9<mei2-5>/Akap9<mei2-5>	involves: 129S1/Sv * C57BL/6	N	12855593
MGI:3050574	M	MP:0008261	arrest of male meiosis	Akap9<mei2-5>/Akap9<mei2-5>	involves: 129S1/Sv * C57BL/6	N	12855593
MGI:3050574	M	MP:0001925	male infertility	Akap9<mei2-5>/Akap9<mei2-5>	involves: 129S1/Sv * C57BL/6	N	12855593
MGI:3050587	M	MP:0001146	abnormal testis morphology	mei2-7/mei2-7	involves: 129S1/Sv * C57BL/6	N	12855593
MGI:3050587	M	MP:0008261	arrest of male meiosis	mei2-7/mei2-7	involves: 129S1/Sv * C57BL/6	N	12855593
MGI:3050587	M	MP:0001925	male infertility	mei2-7/mei2-7	involves: 129S1/Sv * C57BL/6	N	12855593
MGI:3050616	M	MP:0001156	abnormal spermatogenesis	Iqcg<esgd12d>/Iqcg<esgd12d>	involves: C3HeB/FeJ * C57BL/6	N	12855593
MGI:3050616	M	MP:0005578	teratozoospermia	Iqcg<esgd12d>/Iqcg<esgd12d>	involves: C3HeB/FeJ * C57BL/6	N	MGI:3052828
MGI:3050616	M	MP:0005159	azoospermia	Iqcg<esgd12d>/Iqcg<esgd12d>	involves: C3HeB/FeJ * C57BL/6	N	12855593
MGI:3050616	M	MP:0002675	asthenozoospermia	Iqcg<esgd12d>/Iqcg<esgd12d>	involves: C3HeB/FeJ * C57BL/6	N	MGI:3052828
MGI:3050616	M	MP:0002687	oligozoospermia	Iqcg<esgd12d>/Iqcg<esgd12d>	involves: C3HeB/FeJ * C57BL/6	N	MGI:3052828
MGI:3050616	M	MP:0001925	male infertility	Iqcg<esgd12d>/Iqcg<esgd12d>	involves: C3HeB/FeJ * C57BL/6	N	12855593
MGI:3050616	M	MP:0001925	male infertility	Iqcg<esgd12d>/Iqcg<esgd12d>	involves: C3HeB/FeJ * C57BL/6	N	MGI:3052828
MGI:3050616	M	MP:0009239	short sperm flagellum	Iqcg<esgd12d>/Iqcg<esgd12d>	involves: C3HeB/FeJ * C57BL/6	N	MGI:3052828
MGI:3050616	M	MP:0008545	absent sperm flagellum	Iqcg<esgd12d>/Iqcg<esgd12d>	involves: C3HeB/FeJ * C57BL/6	N	MGI:3052828
MGI:3050638	M	MP:0001925	male infertility	swm6/swm6	involves: C3HeB/FeJ * C57BL/6	N	12855593
MGI:3050638	M	MP:0005159	azoospermia	swm6/swm6	involves: C3HeB/FeJ * C57BL/6	N	12855593
MGI:3050638	M	MP:0001156	abnormal spermatogenesis	swm6/swm6	involves: C3HeB/FeJ * C57BL/6	N	12855593
MGI:3050646	M	MP:0009831	abnormal sperm midpiece morphology	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3050646	M	MP:0001156	abnormal spermatogenesis	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	12855593
MGI:3050646	M	MP:0001925	male infertility	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	12855593
MGI:3050646	M	MP:0009232	abnormal sperm nucleus morphology	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3050646	M	MP:0009836	abnormal sperm principal piece morphology	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3050646	M	MP:0006380	abnormal spermatid morphology	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3050646	M	MP:0002687	oligozoospermia	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	12855593
MGI:3050646	M	MP:0005578	teratozoospermia	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3050646	M	MP:0008545	absent sperm flagellum	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	12855593
MGI:3050646	M	MP:0020869	immotile sperm	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3050646	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3050646	M	MP:0009234	absent sperm head	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3050646	M	MP:0009239	short sperm flagellum	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3050646	M	MP:0001925	male infertility	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3050646	M	MP:0002687	oligozoospermia	swm2/swm2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3050655	M	MP:0001925	male infertility	lsgd9a/lsgd9a	involves: C3HeB/FeJ * C57BL/6	N	12855593
MGI:3050655	M	MP:0001156	abnormal spermatogenesis	lsgd9a/lsgd9a	involves: C3HeB/FeJ * C57BL/6	N	12855593
MGI:3050787	F	MP:0002758	long tail	Bw19<HI>/Bw19<HI>	involves: HI * LI	N	11535651
MGI:3050787	F	MP:0011939	increased food intake	Bw19<HI>/Bw19<HI>	involves: HI * LI	N	11535651
MGI:3050787	F	MP:0002865	increased growth rate	Bw19<HI>/Bw19<HI>	involves: HI * LI	N	11535651
MGI:3050787	F	MP:0001257	increased body length	Bw19<HI>/Bw19<HI>	involves: HI * LI	N	11535651
MGI:3050843	M	MP:0031287	bilateral cryptorchism	Dnajc5<tm1Sud>/Dnajc5<tm1Sud>	involves: 129S6/SvEvTac	N	15091340
MGI:3050891	M	MP:0009243	hairpin sperm flagellum	Fhl5<tm1Saco>/Fhl5<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	15247423
MGI:3050891	M	MP:0002687	oligozoospermia	Fhl5<tm1Saco>/Fhl5<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	15247423
MGI:3050891	M	MP:0005578	teratozoospermia	Fhl5<tm1Saco>/Fhl5<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	15247423
MGI:3050891	M	MP:0009230	abnormal sperm head morphology	Fhl5<tm1Saco>/Fhl5<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	15247423
MGI:3050891	M	MP:0002662	abnormal cauda epididymis morphology	Fhl5<tm1Saco>/Fhl5<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	15247423
MGI:3050891	M	MP:0001145	abnormal male reproductive system morphology	Fhl5<tm1Saco>/Fhl5<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	15247423
MGI:3050891	M	MP:0001147	small testis	Fhl5<tm1Saco>/Fhl5<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	15247423
MGI:3050891	M	MP:0009231	detached acrosome	Fhl5<tm1Saco>/Fhl5<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	15247423
MGI:3050891	M	MP:0009232	abnormal sperm nucleus morphology	Fhl5<tm1Saco>/Fhl5<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	15247423
MGI:3050891	M	MP:0008898	abnormal acrosome morphology	Fhl5<tm1Saco>/Fhl5<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	15247423
MGI:3050891	M	MP:0002675	asthenozoospermia	Fhl5<tm1Saco>/Fhl5<tm1Saco>	involves: 129S2/SvPas * C57BL/6	N	15247423
MGI:3051220	M	MP:0001925	male infertility	tth/tth	C57BL/6JEi	N	MGI:3047557
MGI:3051310	F	MP:0000708	thymus hyperplasia	Thyct1<C57BL/6J>/Thyct1<C57BL/6J>,Thyct2<C57BL/6J>/Thyct2<C57BL/6J>	involves: C57BL/6J * DBA/2J	N	12944977
MGI:3051311	F	MP:0001823	thymus hypoplasia	Thyct1<DBA/2J>/Thyct1<DBA/2J>,Thyct2<DBA/2J>/Thyct2<DBA/2J>	involves: C57BL/6J * DBA/2J	N	12944977
MGI:3051419	F	MP:0002907	abnormal parturition	Dll3<pu-J>/Dll3<pu-J>	STOCK Tg(Pfkl)224Yg/J-Dll3<pu-J>/GrsrJ	N	MGI:3037056
MGI:3051530	F	MP:0009015	short proestrus	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0008983	small vagina	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0031239	increased atretic ovarian follicle number	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0009018	short estrus	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0001129	impaired ovarian folliculogenesis	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	M	MP:0001154	seminiferous tubule degeneration	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	15199144
MGI:3051530	M	MP:0020550	multinucleated giant male germ cells	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	17431400
MGI:3051530	F	MP:0001928	abnormal ovulation	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0002636	delayed vaginal opening	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0002637	small uterus	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	M	MP:0008261	arrest of male meiosis	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	15199144
MGI:3051530	F	MP:0002679	abnormal corpus luteum morphology	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0001935	decreased litter size	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0005185	decreased circulating progesterone level	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0005181	decreased circulating estradiol level	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0009006	prolonged estrous cycle	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0013508	increased granulosa cell apoptosis	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	M	MP:0002687	oligozoospermia	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	15199144
MGI:3051530	M	MP:0004852	decreased testis weight	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	15199144
MGI:3051530	F	MP:0001127	small ovary	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	M	MP:0001922	reduced male fertility	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	15199144
MGI:3051530	F	MP:0002682	decreased mature ovarian follicle number	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0002680	decreased corpora lutea number	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0003507	abnormal ovary physiology	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0001923	reduced female fertility	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0009209	abnormal internal female genitalia morphology	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0031420	decreased superovulation rate	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0009011	prolonged diestrus	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051530	F	MP:0001927	abnormal estrous cycle	Nr2c2<tm1Chc>/Nr2c2<tm1Chc>	Not Specified	N	18174360
MGI:3051565	F	MP:0005095	decreased T cell proliferation	Pim2<tm1Brn>/Pim2<tm1Brn>	involves: 129P/Ola * FVB/N	N	15199164
MGI:3051567	F	MP:0001732	postnatal growth retardation	Pim1<tm1Pwl>/Pim1<tm1Pwl>,Pim2<tm1Brn>/Pim2<tm1Brn>,Pim3<tm1Brn>/Pim3<tm1Brn>	involves: 129P/Ola * FVB/N	N	15199164
MGI:3051567	F	MP:0002416	abnormal proerythroblast morphology	Pim1<tm1Pwl>/Pim1<tm1Pwl>,Pim2<tm1Brn>/Pim2<tm1Brn>,Pim3<tm1Brn>/Pim3<tm1Brn>	involves: 129P/Ola * FVB/N	N	15199164
MGI:3051567	F	MP:0003131	increased erythrocyte cell number	Pim1<tm1Pwl>/Pim1<tm1Pwl>,Pim2<tm1Brn>/Pim2<tm1Brn>,Pim3<tm1Brn>/Pim3<tm1Brn>	involves: 129P/Ola * FVB/N	N	15199164
MGI:3051567	F	MP:0008209	decreased pre-B cell number	Pim1<tm1Pwl>/Pim1<tm1Pwl>,Pim2<tm1Brn>/Pim2<tm1Brn>,Pim3<tm1Brn>/Pim3<tm1Brn>	involves: 129P/Ola * FVB/N	N	15199164
MGI:3051567	F	MP:0008208	decreased pro-B cell number	Pim1<tm1Pwl>/Pim1<tm1Pwl>,Pim2<tm1Brn>/Pim2<tm1Brn>,Pim3<tm1Brn>/Pim3<tm1Brn>	involves: 129P/Ola * FVB/N	N	15199164
MGI:3051567	F	MP:0009703	decreased birth body size	Pim1<tm1Pwl>/Pim1<tm1Pwl>,Pim2<tm1Brn>/Pim2<tm1Brn>,Pim3<tm1Brn>/Pim3<tm1Brn>	involves: 129P/Ola * FVB/N	N	15199164
MGI:3051567	F	MP:0005017	decreased B cell number	Pim1<tm1Pwl>/Pim1<tm1Pwl>,Pim2<tm1Brn>/Pim2<tm1Brn>,Pim3<tm1Brn>/Pim3<tm1Brn>	involves: 129P/Ola * FVB/N	N	15199164
MGI:3051567	F	MP:0002591	decreased mean corpuscular volume	Pim1<tm1Pwl>/Pim1<tm1Pwl>,Pim2<tm1Brn>/Pim2<tm1Brn>,Pim3<tm1Brn>/Pim3<tm1Brn>	involves: 129P/Ola * FVB/N	N	15199164
MGI:3051567	F	MP:0005095	decreased T cell proliferation	Pim1<tm1Pwl>/Pim1<tm1Pwl>,Pim2<tm1Brn>/Pim2<tm1Brn>,Pim3<tm1Brn>/Pim3<tm1Brn>	involves: 129P/Ola * FVB/N	N	15199164
MGI:3051567	F	MP:0003133	increased early pro-B cell number	Pim1<tm1Pwl>/Pim1<tm1Pwl>,Pim2<tm1Brn>/Pim2<tm1Brn>,Pim3<tm1Brn>/Pim3<tm1Brn>	involves: 129P/Ola * FVB/N	N	15199164
MGI:3051567	F	MP:0008255	decreased megakaryocyte cell number	Pim1<tm1Pwl>/Pim1<tm1Pwl>,Pim2<tm1Brn>/Pim2<tm1Brn>,Pim3<tm1Brn>/Pim3<tm1Brn>	involves: 129P/Ola * FVB/N	N	15199164
MGI:3051567	F	MP:0005093	decreased B cell proliferation	Pim1<tm1Pwl>/Pim1<tm1Pwl>,Pim2<tm1Brn>/Pim2<tm1Brn>,Pim3<tm1Brn>/Pim3<tm1Brn>	involves: 129P/Ola * FVB/N	N	15199164
MGI:3051575	F	MP:0003128	splayed clitoris	Efnb2<tm1Henk>/Efnb2<tm1Henk>	either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1)	N	15223334
MGI:3051576	M	MP:0001925	male infertility	Efnb2<tm1Henk>/Efnb2<+>	either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1)	N	15223334
MGI:3051576	F	MP:0003128	splayed clitoris	Efnb2<tm1Henk>/Efnb2<+>	either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1)	N	15223334
MGI:3051576	M	MP:0005187	abnormal penis morphology	Efnb2<tm1Henk>/Efnb2<+>	either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1)	N	15223334
MGI:3051589	F	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis	Ghrh<tm1Salv>/Ghrh<tm1Salv>	involves: 129 * C57BL/6	N	21846799
MGI:3051590	M	MP:0001152	increased Leydig cell number	Cnot7<tm1Jpr>/Cnot7<tm1Jpr>	involves: 129/Sv * C57BL/6	N	15199137
MGI:3051590	M	MP:0005250	decreased Sertoli cell number	Cnot7<tm1Jpr>/Cnot7<tm1Jpr>	involves: 129/Sv * C57BL/6	N	15199137
MGI:3051590	M	MP:0004852	decreased testis weight	Cnot7<tm1Jpr>/Cnot7<tm1Jpr>	involves: 129/Sv * C57BL/6	N	15199137
MGI:3051590	M	MP:0002687	oligozoospermia	Cnot7<tm1Jpr>/Cnot7<tm1Jpr>	involves: 129/Sv * C57BL/6	N	15199137
MGI:3051590	M	MP:0001154	seminiferous tubule degeneration	Cnot7<tm1Jpr>/Cnot7<tm1Jpr>	involves: 129/Sv * C57BL/6	N	15199137
MGI:3051590	M	MP:0006362	abnormal male germ cell morphology	Cnot7<tm1Jpr>/Cnot7<tm1Jpr>	involves: 129/Sv * C57BL/6	N	15199137
MGI:3051590	M	MP:0001153	small seminiferous tubules	Cnot7<tm1Jpr>/Cnot7<tm1Jpr>	involves: 129/Sv * C57BL/6	N	15199137
MGI:3051590	M	MP:0001925	male infertility	Cnot7<tm1Jpr>/Cnot7<tm1Jpr>	involves: 129/Sv * C57BL/6	N	15199137
MGI:3051590	M	MP:0001146	abnormal testis morphology	Cnot7<tm1Jpr>/Cnot7<tm1Jpr>	involves: 129/Sv * C57BL/6	N	15199137
MGI:3051590	M	MP:0004901	decreased male germ cell number	Cnot7<tm1Jpr>/Cnot7<tm1Jpr>	involves: 129/Sv * C57BL/6	N	15199137
MGI:3051594	M	MP:0001925	male infertility	Atp2b4<tm1Ges>/Atp2b4<tm1Ges>	involves: 129X1/SvJ * Black Swiss	N	15178683
MGI:3051595	M	MP:0002675	asthenozoospermia	Atp2b4<tm1Ges>/Atp2b4<tm1Ges>	BKSW.129X1-Atp2b4<tm1Ges>	N	15178683
MGI:3051595	M	MP:0001925	male infertility	Atp2b4<tm1Ges>/Atp2b4<tm1Ges>	BKSW.129X1-Atp2b4<tm1Ges>	N	15178683
MGI:3051598	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm1(Ggt1-Agtr1)Cof>/Y	involves: 129P2/OlaHsd	N	15306694
MGI:3051599	M	MP:0001596	hypotension	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Hprt1<tm1(Ggt1-Agtr1)Cof>/Y	involves: 129P2/OlaHsd	N	15306694
MGI:3051599	M	MP:0002988	decreased urine osmolality	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Hprt1<tm1(Ggt1-Agtr1)Cof>/Y	involves: 129P2/OlaHsd	N	15306694
MGI:3051600	M	MP:0003675	kidney cyst	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Hprt1<tm1(Ggt1-Agtr1)Cof>/Y	involves: 129P2/OlaHsd	N	15306694
MGI:3051600	M	MP:0005583	decreased renin activity	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Hprt1<tm1(Ggt1-Agtr1)Cof>/Y	involves: 129P2/OlaHsd	N	15306694
MGI:3051611	F	MP:0000627	abnormal mammary gland morphology	Btn1a1<tm1Ihm>/Btn1a1<tm1Ihm>	involves: 129P2/OlaHsd * C57BL/6	N	15226505
MGI:3051611	F	MP:0004047	abnormal milk composition	Btn1a1<tm1Ihm>/Btn1a1<tm1Ihm>	involves: 129P2/OlaHsd * C57BL/6	N	15226505
MGI:3051611	F	MP:0001882	abnormal lactation	Btn1a1<tm1Ihm>/Btn1a1<tm1Ihm>	involves: 129P2/OlaHsd * C57BL/6	N	15226505
MGI:3051614	F	MP:0004047	abnormal milk composition	Btn1a1<tm2Ihm>/Btn1a1<tm2Ihm>	involves: 129S6/SvEvTac * C57BL/6	N	15226505
MGI:3051614	F	MP:0000627	abnormal mammary gland morphology	Btn1a1<tm2Ihm>/Btn1a1<tm2Ihm>	involves: 129S6/SvEvTac * C57BL/6	N	15226505
MGI:3051614	F	MP:0001882	abnormal lactation	Btn1a1<tm2Ihm>/Btn1a1<tm2Ihm>	involves: 129S6/SvEvTac * C57BL/6	N	15226505
MGI:3051788	M	MP:0012307	impaired spatial learning	Ube2a<tm1Agr>/Y	involves: 129P2/OlaHsd * FVB/N	N	26476408
MGI:3051788	M	MP:0001475	reduced long-term depression	Ube2a<tm1Agr>/Y	involves: 129P2/OlaHsd * FVB/N	N	26476408
MGI:3051788	M	MP:0009454	impaired contextual conditioning behavior	Ube2a<tm1Agr>/Y	involves: 129P2/OlaHsd * FVB/N	N	26476408
MGI:3051788	M	MP:0001262	decreased body weight	Ube2a<tm1Agr>/Y	involves: 129P2/OlaHsd * FVB/N	N	15169909
MGI:3051788	M	MP:0011101	prenatal lethality, incomplete penetrance	Ube2a<tm1Agr>/Y	involves: 129P2/OlaHsd * FVB/N	N	15169909
MGI:3051789	M	MP:0011091	prenatal lethality, complete penetrance	Ube2a<tm1Agr>/Y,Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/N	N	15169909
MGI:3051838	M	MP:0009674	decreased birth weight	Ube2a<tm1Agr>/Y,Ube2b<tm1Jhjh>/Ube2b<+>	involves: 129P2/OlaHsd * FVB/N	N	15169909
MGI:3051838	M	MP:0011101	prenatal lethality, incomplete penetrance	Ube2a<tm1Agr>/Y,Ube2b<tm1Jhjh>/Ube2b<+>	involves: 129P2/OlaHsd * FVB/N	N	15169909
MGI:3051838	M	MP:0001262	decreased body weight	Ube2a<tm1Agr>/Y,Ube2b<tm1Jhjh>/Ube2b<+>	involves: 129P2/OlaHsd * FVB/N	N	15169909
MGI:3051838	M	MP:0005389	reproductive system phenotype	Ube2a<tm1Agr>/Y,Ube2b<tm1Jhjh>/Ube2b<+>	involves: 129P2/OlaHsd * FVB/N	Y	15169909
MGI:3051845	F	MP:0001926	female infertility	Ube2a<tm1Agr>/Ube2a<tm1Agr>	involves: 129P2/OlaHsd * FVB/N	N	15169909
MGI:3051845	F	MP:0001262	decreased body weight	Ube2a<tm1Agr>/Ube2a<tm1Agr>	involves: 129P2/OlaHsd * FVB/N	N	15169909
MGI:3051847	F	MP:0011101	prenatal lethality, incomplete penetrance	Ube2a<tm1Agr>/Ube2a<tm1Agr>,Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/N	N	15169909
MGI:3051848	F	MP:0011101	prenatal lethality, incomplete penetrance	Ube2a<tm1Agr>/Ube2a<+>,Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/N	N	15169909
MGI:3051849	F	MP:0001262	decreased body weight	Ube2a<tm1Agr>/Ube2a<tm1Agr>,Ube2b<tm1Jhjh>/Ube2b<+>	involves: 129P2/OlaHsd * FVB/N	N	15169909
MGI:3051849	F	MP:0011101	prenatal lethality, incomplete penetrance	Ube2a<tm1Agr>/Ube2a<tm1Agr>,Ube2b<tm1Jhjh>/Ube2b<+>	involves: 129P2/OlaHsd * FVB/N	N	15169909
MGI:3051983	M	MP:0004852	decreased testis weight	Utp14b<jsd>/Utp14b<jsd>	involves: C3H/HeJ * C57BL/6J	N	15289605
MGI:3051983	M	MP:0001925	male infertility	Utp14b<jsd>/Utp14b<jsd>	involves: C3H/HeJ * C57BL/6J	N	15289605
MGI:3051983	M	MP:0005159	azoospermia	Utp14b<jsd>/Utp14b<jsd>	involves: C3H/HeJ * C57BL/6J	N	15289605
MGI:3052308	F	MP:0001382	abnormal nursing	Hr<rhsl>/Hr<rhsl>	involves: BALB/c	N	15955095
MGI:3052419	M	MP:0001148	enlarged testis	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/Ola * C57BL/6	N	15192078
MGI:3052419	F	MP:0004906	enlarged uterus	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/Ola * C57BL/6	N	15192078
MGI:3052706	M	MP:0001925	male infertility	Adam1a<tm1Tba>/Adam1a<tm1Tba>	involves: 129S2/SvPas * ICR	N	15194697
MGI:3052706	M	MP:0030978	impaired binding of sperm to zona pellucida	Adam1a<tm1Tba>/Adam1a<tm1Tba>	involves: 129S2/SvPas * ICR	N	15194697
MGI:3052706	M	MP:0031012	impaired sperm migration in female genital tract	Adam1a<tm1Tba>/Adam1a<tm1Tba>	involves: 129S2/SvPas * ICR	N	15194697
MGI:3052838	M	MP:0002686	globozoospermia	repro13/repro13	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3052838	M	MP:0001925	male infertility	repro13/repro13	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3052838	M	MP:0001156	abnormal spermatogenesis	repro13/repro13	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3052838	M	MP:0002687	oligozoospermia	repro13/repro13	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3052846	M	MP:0003205	testicular atrophy	Pex7<tm1Rjaw>/Pex7<tm1Rjaw>	Swiss	N	12915479
MGI:3052938	F	MP:0001718	abnormal visceral yolk sac morphology	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052938	F	MP:0011091	prenatal lethality, complete penetrance	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	9175730
MGI:3052938	F	MP:0005602	decreased angiogenesis	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052938	F	MP:0011204	abnormal visceral yolk sac blood island morphology	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052938	F	MP:0002584	small ectoplacental cone	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052938	F	MP:0009657	failure of chorioallantoic fusion	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052938	F	MP:0001716	abnormal placenta labyrinth morphology	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052938	F	MP:0004259	small placenta	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052938	F	MP:0003984	embryonic growth retardation	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052938	F	MP:0004255	abnormal spongiotrophoblast layer morphology	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052938	F	MP:0005031	abnormal trophoblast layer morphology	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052938	F	MP:0004076	abnormal vitelline vascular remodeling	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052938	F	MP:0001327	decreased retina photoreceptor cell number	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	9175730
MGI:3052938	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052948	F	MP:0011101	prenatal lethality, incomplete penetrance	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6 * SMZ	N	15242790
MGI:3052948	F	MP:0005391	vision/eye phenotype	Chm<tm1Jvdh>/Chm<+>	involves: 129P2/OlaHsd * C57BL/6 * SMZ	Y	15242790
MGI:3052952	M	MP:0002584	small ectoplacental cone	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052952	M	MP:0005031	abnormal trophoblast layer morphology	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052952	M	MP:0004255	abnormal spongiotrophoblast layer morphology	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052952	M	MP:0011204	abnormal visceral yolk sac blood island morphology	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052952	M	MP:0003403	absent placental labyrinth	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052952	M	MP:0009657	failure of chorioallantoic fusion	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052952	M	MP:0011523	thin placenta labyrinth	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052952	M	MP:0001716	abnormal placenta labyrinth morphology	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052952	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052952	M	MP:0004076	abnormal vitelline vascular remodeling	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052952	M	MP:0011091	prenatal lethality, complete penetrance	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	9175730
MGI:3052952	M	MP:0001718	abnormal visceral yolk sac morphology	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052952	M	MP:0003984	embryonic growth retardation	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052952	M	MP:0005602	decreased angiogenesis	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052952	M	MP:0004259	small placenta	Chm<tm1Jvdh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15242790
MGI:3052994	F	MP:0001923	reduced female fertility	Dspd/Dspd<+>	involves: C3H * C57BL/6	N	14695912
MGI:3052994	M	MP:0001925	male infertility	Dspd/Dspd<+>	involves: C3H * C57BL/6	N	14695912
MGI:3052994	M	MP:0002687	oligozoospermia	Dspd/Dspd<+>	involves: C3H * C57BL/6	N	14695912
MGI:3052994	M	MP:0001932	abnormal spermiogenesis	Dspd/Dspd<+>	involves: C3H * C57BL/6	N	14695912
MGI:3052994	M	MP:0009230	abnormal sperm head morphology	Dspd/Dspd<+>	involves: C3H * C57BL/6	N	14695912
MGI:3053007	M	MP:0001925	male infertility	Kit<W-pw>/Kit<+>	involves: STOCK Prop1<df> Myo5a<d> Bmp5<se>	N	MGI:61837
MGI:3053007	F	MP:0001926	female infertility	Kit<W-pw>/Kit<+>	involves: STOCK Prop1<df> Myo5a<d> Bmp5<se>	N	MGI:61837
MGI:3053027	M	MP:0001925	male infertility	Kit<W-pw>/Kit<W-v>	involves: STOCK Prop1<df> Myo5a<d> Bmp5<se>	N	MGI:61837
MGI:3053027	F	MP:0001926	female infertility	Kit<W-pw>/Kit<W-v>	involves: STOCK Prop1<df> Myo5a<d> Bmp5<se>	N	MGI:61837
MGI:3053462	F	MP:0004805	absent oocytes	Nobox<tm1Rajk>/Nobox<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	15326356
MGI:3053462	F	MP:0001129	impaired ovarian folliculogenesis	Nobox<tm1Rajk>/Nobox<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	15326356
MGI:3053462	F	MP:0004833	ovary atrophy	Nobox<tm1Rajk>/Nobox<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	15326356
MGI:3053462	F	MP:0002016	ovary cyst	Nobox<tm1Rajk>/Nobox<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	15326356
MGI:3053462	F	MP:0009093	oocyte degeneration	Nobox<tm1Rajk>/Nobox<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	15326356
MGI:3053462	F	MP:0001125	abnormal oocyte morphology	Nobox<tm1Rajk>/Nobox<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	15326356
MGI:3053462	F	MP:0008871	abnormal ovarian follicle number	Nobox<tm1Rajk>/Nobox<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	15326356
MGI:3053462	F	MP:0001926	female infertility	Nobox<tm1Rajk>/Nobox<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	15326356
MGI:3053462	F	MP:0005431	decreased oocyte number	Nobox<tm1Rajk>/Nobox<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	15326356
MGI:3053462	F	MP:0031382	absent secondary ovarian follicles	Nobox<tm1Rajk>/Nobox<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	15326356
MGI:3053962	F	MP:0002639	micrognathia	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053962	F	MP:0011091	prenatal lethality, complete penetrance	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053962	F	MP:0000454	abnormal jaw morphology	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053962	F	MP:0001284	absent vibrissae	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053962	F	MP:0000428	abnormal craniofacial morphology	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053962	F	MP:0012138	decreased forebrain size	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053962	F	MP:0000435	shortened head	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053962	F	MP:0000097	short maxilla	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053962	F	MP:0000088	short mandible	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053962	F	MP:0005058	abnormal lysosome morphology	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053963	M	MP:0002639	micrognathia	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053963	M	MP:0011091	prenatal lethality, complete penetrance	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053963	M	MP:0000428	abnormal craniofacial morphology	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053963	M	MP:0012138	decreased forebrain size	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053963	M	MP:0000435	shortened head	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053963	M	MP:0001284	absent vibrissae	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053963	M	MP:0000097	short maxilla	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053963	M	MP:0000088	short mandible	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053963	M	MP:0005058	abnormal lysosome morphology	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3053963	M	MP:0000454	abnormal jaw morphology	Lamp1<tm1Psa>/Lamp1<tm1Psa>,Lamp2<tm1Psa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15121881
MGI:3054095	F	MP:0001923	reduced female fertility	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	15315761
MGI:3054095	F	MP:0002682	decreased mature ovarian follicle number	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	15315761
MGI:3054096	F	MP:0001931	abnormal oogenesis	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	15315761
MGI:3054096	M	MP:0001156	abnormal spermatogenesis	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	15315761
MGI:3054170	M	MP:0010758	increased right ventricle systolic pressure	Vip<tm1Clw>/Vip<tm1Clw>	involves: 129S/Sv * C57BL/6	N	17309917
MGI:3054170	M	MP:0004007	abnormal lung vasculature morphology	Vip<tm1Clw>/Vip<tm1Clw>	involves: 129S/Sv * C57BL/6	N	17309917
MGI:3054170	M	MP:0003548	pulmonary hypertension	Vip<tm1Clw>/Vip<tm1Clw>	involves: 129S/Sv * C57BL/6	N	17309917
MGI:3054170	M	MP:0000276	heart right ventricle hypertrophy	Vip<tm1Clw>/Vip<tm1Clw>	involves: 129S/Sv * C57BL/6	N	17309917
MGI:3054170	M	MP:0001861	lung inflammation	Vip<tm1Clw>/Vip<tm1Clw>	involves: 129S/Sv * C57BL/6	N	17309917
MGI:3054170	M	MP:0000484	abnormal pulmonary artery morphology	Vip<tm1Clw>/Vip<tm1Clw>	involves: 129S/Sv * C57BL/6	N	17309917
MGI:3054170	M	MP:0002083	premature death	Vip<tm1Clw>/Vip<tm1Clw>	involves: 129S/Sv * C57BL/6	N	17309917
MGI:3054402	F	MP:0001927	abnormal estrous cycle	Pcsk6<tm1Rob>/Pcsk6<tm1Rob>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21183657
MGI:3054402	F	MP:0002016	ovary cyst	Pcsk6<tm1Rob>/Pcsk6<tm1Rob>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21183657
MGI:3054402	F	MP:0010287	increased reproductive system tumor incidence	Pcsk6<tm1Rob>/Pcsk6<tm1Rob>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21183657
MGI:3054402	F	MP:0001126	abnormal ovary morphology	Pcsk6<tm1Rob>/Pcsk6<tm1Rob>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21183657
MGI:3054402	F	MP:0002777	absent ovarian follicles	Pcsk6<tm1Rob>/Pcsk6<tm1Rob>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21183657
MGI:3054402	F	MP:0010308	decreased tumor latency	Pcsk6<tm1Rob>/Pcsk6<tm1Rob>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21183657
MGI:3054402	F	MP:0003699	abnormal female reproductive system physiology	Pcsk6<tm1Rob>/Pcsk6<tm1Rob>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21183657
MGI:3054402	F	MP:0008995	early reproductive senescence	Pcsk6<tm1Rob>/Pcsk6<tm1Rob>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21183657
MGI:3054402	F	MP:0008000	increased ovary tumor incidence	Pcsk6<tm1Rob>/Pcsk6<tm1Rob>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21183657
MGI:3054405	F	MP:0001923	reduced female fertility	Pcsk2<tm1Dfs>/Pcsk2<tm1Dfs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9192619
MGI:3054426	M	MP:0001152	increased Leydig cell number	Kitl<Sl-17H>/Kitl<Sl-17H>	C3H/HeH-Kitl<Sl-17H>	N	1383087
MGI:3054426	M	MP:0004901	decreased male germ cell number	Kitl<Sl-17H>/Kitl<Sl-17H>	C3H/HeH-Kitl<Sl-17H>	N	1383087
MGI:3054426	F	MP:0001127	small ovary	Kitl<Sl-17H>/Kitl<Sl-17H>	C3H/HeH-Kitl<Sl-17H>	N	1383087
MGI:3054426	F	MP:0005431	decreased oocyte number	Kitl<Sl-17H>/Kitl<Sl-17H>	C3H/HeH-Kitl<Sl-17H>	N	1383087
MGI:3054426	M	MP:0001156	abnormal spermatogenesis	Kitl<Sl-17H>/Kitl<Sl-17H>	C3H/HeH-Kitl<Sl-17H>	N	1383087
MGI:3054426	M	MP:0001925	male infertility	Kitl<Sl-17H>/Kitl<Sl-17H>	C3H/HeH-Kitl<Sl-17H>	N	1383087
MGI:3054527	F	MP:0001505	hunched posture	Tg(DM15)26Bew/0	involves: FVB	N	8673131
MGI:3054527	F	MP:0002074	abnormal hair texture	Tg(DM15)26Bew/0	involves: FVB	N	8673131
MGI:3054527	F	MP:0008028	pregnancy-related premature death	Tg(DM15)26Bew/0	involves: FVB	N	8673131
MGI:3054527	F	MP:0011940	decreased food intake	Tg(DM15)26Bew/0	involves: FVB	N	8673131
MGI:3054794	F	MP:0001386	abnormal maternal nurturing	Npas3<tm1Slm>/Npas3<tm1Slm>	involves: 129S/SvEv * C57BL/6	N	15347806
MGI:3054795	F	MP:0001386	abnormal maternal nurturing	Npas1<tm1Slm>/Npas1<tm1Slm>,Npas3<tm1Slm>/Npas3<tm1Slm>	involves: 129S6/SvEvTac * C57BL/6	N	15347806
MGI:3054827	M	MP:0001925	male infertility	Prkaca<tm2Gsm>/Prkaca<tm2Gsm>	involves: 129X1/SvJ * C57BL/6	N	15340140
MGI:3054827	M	MP:0002675	asthenozoospermia	Prkaca<tm2Gsm>/Prkaca<tm2Gsm>	involves: 129X1/SvJ * C57BL/6	N	15340140
MGI:3054829	M	MP:0001925	male infertility	mix/mix<+>	involves: C57BL/6J * NMRI	N	11718241
MGI:3054969	F	MP:0002907	abnormal parturition	Rxfp1<tm1Aia>/Rxfp1<tm1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	15256493
MGI:3054969	F	MP:0013713	decreased nipple size	Rxfp1<tm1Aia>/Rxfp1<tm1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	15256493
MGI:3054969	F	MP:0001882	abnormal lactation	Rxfp1<tm1Aia>/Rxfp1<tm1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	15256493
MGI:3054969	F	MP:0009722	abnormal nipple development	Rxfp1<tm1Aia>/Rxfp1<tm1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	15256493
MGI:3054971	F	MP:0013713	decreased nipple size	Rxfp1<tm1Aia>/Rxfp1<tm1Aia>,Rxfp2<tm1Aia>/Rxfp2<tm1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	15256493
MGI:3054971	M	MP:0002286	cryptorchism	Rxfp1<tm1Aia>/Rxfp1<tm1Aia>,Rxfp2<tm1Aia>/Rxfp2<tm1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	15256493
MGI:3054971	F	MP:0001882	abnormal lactation	Rxfp1<tm1Aia>/Rxfp1<tm1Aia>,Rxfp2<tm1Aia>/Rxfp2<tm1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	15256493
MGI:3054986	F	MP:0001882	abnormal lactation	Rxfp1<tm1Aia>/Rxfp1<tm1Aia>,Tg(Ins2-Insl3)4Imad/0	involves: 129S7/SvEvBrd * C57BL/6J	N	15256493
MGI:3054986	F	MP:0013713	decreased nipple size	Rxfp1<tm1Aia>/Rxfp1<tm1Aia>,Tg(Ins2-Insl3)4Imad/0	involves: 129S7/SvEvBrd * C57BL/6J	N	15256493
MGI:3054986	F	MP:0011727	ectopic ovary	Rxfp1<tm1Aia>/Rxfp1<tm1Aia>,Tg(Ins2-Insl3)4Imad/0	involves: 129S7/SvEvBrd * C57BL/6J	N	15256493
MGI:3054987	F	MP:0001382	abnormal nursing	Ctnnb1<tm2Kem>/Ctnnb1<tm2Kem>,Emx1<tm1(cre)Yql>/Emx1<+>	B6.129-Emx1<tm1(cre)Yql> Ctnnb1<tm2Kem>	N	15219872
MGI:3054987	M	MP:0001925	male infertility	Ctnnb1<tm2Kem>/Ctnnb1<tm2Kem>,Emx1<tm1(cre)Yql>/Emx1<+>	B6.129-Emx1<tm1(cre)Yql> Ctnnb1<tm2Kem>	N	15219872
MGI:3054988	F	MP:0001923	reduced female fertility	Tg(Ins2-Insl3)4Imad/0	involves: FVB/N	N	11818498
MGI:3054988	F	MP:0011727	ectopic ovary	Tg(Ins2-Insl3)4Imad/0	involves: FVB/N	N	11818498
MGI:3055091	M	MP:0002687	oligozoospermia	Scn8a<med-jo2J>/Scn8a<med-jo2J>	B6(129S7)-Scn8a<med-jo2J>/J	N	MGI:3051855
MGI:3055120	M	MP:0004901	decreased male germ cell number	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	5565073
MGI:3055120	F	MP:0001931	abnormal oogenesis	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	9689098
MGI:3055120	M	MP:0009230	abnormal sperm head morphology	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	5565073
MGI:3055120	M	MP:0009233	enlarged sperm head	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	5565073
MGI:3055120	M	MP:0001147	small testis	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	5565073
MGI:3055120	M	MP:0001925	male infertility	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	5565073
MGI:3055120	M	MP:0001940	testis hypoplasia	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	5565073
MGI:3055120	M	MP:0008892	abnormal sperm flagellum morphology	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	5565073
MGI:3055120	M	MP:0020550	multinucleated giant male germ cells	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	9689098
MGI:3055120	M	MP:0006380	abnormal spermatid morphology	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	5565073
MGI:3055120	M	MP:0001153	small seminiferous tubules	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	5565073
MGI:3055120	M	MP:0008898	abnormal acrosome morphology	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	5565073
MGI:3055120	M	MP:0001156	abnormal spermatogenesis	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	9689098
MGI:3055120	M	MP:0001932	abnormal spermiogenesis	Oca2<p-6H>/Oca2<p-6H>	involves: 101/H * C3H/HeH	N	5565073
MGI:3055190	M	MP:0002675	asthenozoospermia	Pla2g6<tm1Turk>/Pla2g6<tm1Turk>	involves: 129X1/SvJ	N	15252026
MGI:3055190	M	MP:0001922	reduced male fertility	Pla2g6<tm1Turk>/Pla2g6<tm1Turk>	involves: 129X1/SvJ	N	15252026
MGI:3055294	F	MP:0001923	reduced female fertility	Dmbx1<tm1Bhr>/Dmbx1<tm1Bhr>	involves: 129S4/SvJae * C57BL/6	N	15314164
MGI:3055324	M	MP:0001925	male infertility	Tekt2<Gt(OST12401)Lex>/Tekt2<Gt(OST12401)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	15340058
MGI:3055324	M	MP:0002675	asthenozoospermia	Tekt2<Gt(OST12401)Lex>/Tekt2<Gt(OST12401)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	15340058
MGI:3055324	M	MP:0009838	abnormal sperm axoneme morphology	Tekt2<Gt(OST12401)Lex>/Tekt2<Gt(OST12401)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	15340058
MGI:3055324	M	MP:0009243	hairpin sperm flagellum	Tekt2<Gt(OST12401)Lex>/Tekt2<Gt(OST12401)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	15340058
MGI:3055363	F	MP:0003838	abnormal milk ejection	Stat5a<tm2Mam>/Stat5a<tm2Mam>,Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(MMTV-cre)4Mam/0	involves: 129S6/SvEvTac * Black Swiss * FVB	N	15340066
MGI:3055363	F	MP:0000662	abnormal branching of the mammary ductal tree	Stat5a<tm2Mam>/Stat5a<tm2Mam>,Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(MMTV-cre)4Mam/0	involves: 129S6/SvEvTac * Black Swiss * FVB	N	15340066
MGI:3055364	F	MP:0014126	increased mammary gland apoptosis	Stat5a<tm2Mam>/Stat5a<tm2Mam>,Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(Wap-cre)11738Mam/0	involves: 129S6/SvEvTac * Black Swiss	N	15340066
MGI:3055364	F	MP:0010172	abnormal mammary gland epithelium physiology	Stat5a<tm2Mam>/Stat5a<tm2Mam>,Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(Wap-cre)11738Mam/0	involves: 129S6/SvEvTac * Black Swiss	N	15340066
MGI:3055364	F	MP:0009506	abnormal mammary gland alveolus morphology	Stat5a<tm2Mam>/Stat5a<tm2Mam>,Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(Wap-cre)11738Mam/0	involves: 129S6/SvEvTac * Black Swiss	N	15340066
MGI:3055366	F	MP:0003838	abnormal milk ejection	Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(MMTV-cre)4Mam/0	involves: 129S6/SvEvTac * Black Swiss * FVB	N	15340066
MGI:3055366	F	MP:0000662	abnormal branching of the mammary ductal tree	Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(MMTV-cre)4Mam/0	involves: 129S6/SvEvTac * Black Swiss * FVB	N	15340066
MGI:3055367	F	MP:0009506	abnormal mammary gland alveolus morphology	Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(Wap-cre)11738Mam/0	involves: 129S6/SvEvTac * Black Swiss	N	15340066
MGI:3055367	F	MP:0014126	increased mammary gland apoptosis	Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(Wap-cre)11738Mam/0	involves: 129S6/SvEvTac * Black Swiss	N	15340066
MGI:3055423	M	MP:0001925	male infertility	Jam3<tm1Rha>/Jam3<tm1Rha>	involves: 129P2/OlaHsd * C57BL/6	N	17455169
MGI:3055423	M	MP:0002216	abnormal seminiferous tubule morphology	Jam3<tm1Rha>/Jam3<tm1Rha>	involves: 129P2/OlaHsd * C57BL/6	N	15372036
MGI:3055423	M	MP:0001155	arrest of spermatogenesis	Jam3<tm1Rha>/Jam3<tm1Rha>	involves: 129P2/OlaHsd * C57BL/6	N	15372036
MGI:3055423	M	MP:0001925	male infertility	Jam3<tm1Rha>/Jam3<tm1Rha>	involves: 129P2/OlaHsd * C57BL/6	N	15372036
MGI:3055423	M	MP:0001147	small testis	Jam3<tm1Rha>/Jam3<tm1Rha>	involves: 129P2/OlaHsd * C57BL/6	N	15372036
MGI:3055423	M	MP:0002686	globozoospermia	Jam3<tm1Rha>/Jam3<tm1Rha>	involves: 129P2/OlaHsd * C57BL/6	N	15372036
MGI:3055514	F	MP:0001127	small ovary	Kit<W-44J>/Kit<W-44J>	B6.C3-Kit<W-44J>/J	N	7274658
MGI:3055514	F	MP:0008871	abnormal ovarian follicle number	Kit<W-44J>/Kit<W-44J>	B6.C3-Kit<W-44J>/J	N	7274658
MGI:3055514	F	MP:0001923	reduced female fertility	Kit<W-44J>/Kit<W-44J>	B6.C3-Kit<W-44J>/J	N	7274658
MGI:3055514	M	MP:0001925	male infertility	Kit<W-44J>/Kit<W-44J>	B6.C3-Kit<W-44J>/J	N	7274658
MGI:3055514	F	MP:0001126	abnormal ovary morphology	Kit<W-44J>/Kit<W-44J>	B6.C3-Kit<W-44J>/J	N	7274658
MGI:3055516	M	MP:0009199	abnormal external male genitalia morphology	Lrp6<Gt(Ex187)Byg>/Lrp6<Gt(Ex187)Byg>	involves: 129P2/OlaHsd	N	19653321
MGI:3055516	F	MP:0003126	abnormal external female genitalia morphology	Lrp6<Gt(Ex187)Byg>/Lrp6<Gt(Ex187)Byg>	involves: 129P2/OlaHsd	N	19653321
MGI:3055550	M	MP:0001925	male infertility	Cldn11<tm1Sts>/Cldn11<tm1Sts>	involves: 129S4/SvJae * C57BL/6	N	15456848
MGI:3055579	F	MP:0009293	decreased inguinal fat pad weight	Gng3<tm1.1Rbs>/Gng3<tm1.1Rbs>	involves: FVB/N	N	15314181
MGI:3055579	F	MP:0009305	decreased retroperitoneal fat pad weight	Gng3<tm1.1Rbs>/Gng3<tm1.1Rbs>	involves: FVB/N	N	15314181
MGI:3055579	F	MP:0005668	decreased circulating leptin level	Gng3<tm1.1Rbs>/Gng3<tm1.1Rbs>	involves: FVB/N	N	15314181
MGI:3055580	F	MP:0009293	decreased inguinal fat pad weight	Gng3<tm1.1Rbs>/Gng3<tm1.1Rbs>	involves: C57BL/6J * FVB/N	N	15314181
MGI:3055580	F	MP:0009305	decreased retroperitoneal fat pad weight	Gng3<tm1.1Rbs>/Gng3<tm1.1Rbs>	involves: C57BL/6J * FVB/N	N	15314181
MGI:3055580	F	MP:0005668	decreased circulating leptin level	Gng3<tm1.1Rbs>/Gng3<tm1.1Rbs>	involves: C57BL/6J * FVB/N	N	15314181
MGI:3055761	F	MP:0005387	immune system phenotype	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	involves: 129S6/SvEvTac * C57BL/6	Y	15356144
MGI:3055784	F	MP:0005606	increased bleeding time	F9<tm2(F9)Dws>/F9<tm2(F9)Dws>	involves: 129S6/SvEvTac * C57BL/6	N	15178576
MGI:3055913	M	MP:0008898	abnormal acrosome morphology	Nectin2<tm1Vrr>/Nectin2<tm1Vrr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10733589
MGI:3055913	M	MP:0001932	abnormal spermiogenesis	Nectin2<tm1Vrr>/Nectin2<tm1Vrr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10733589
MGI:3055913	M	MP:0009831	abnormal sperm midpiece morphology	Nectin2<tm1Vrr>/Nectin2<tm1Vrr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10733589
MGI:3055913	M	MP:0009230	abnormal sperm head morphology	Nectin2<tm1Vrr>/Nectin2<tm1Vrr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10733589
MGI:3055913	M	MP:0009232	abnormal sperm nucleus morphology	Nectin2<tm1Vrr>/Nectin2<tm1Vrr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10733589
MGI:3055913	M	MP:0014468	disorganized sperm mitochondrial sheath	Nectin2<tm1Vrr>/Nectin2<tm1Vrr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10733589
MGI:3055913	M	MP:0001925	male infertility	Nectin2<tm1Vrr>/Nectin2<tm1Vrr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10733589
MGI:3055913	M	MP:0008892	abnormal sperm flagellum morphology	Nectin2<tm1Vrr>/Nectin2<tm1Vrr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10733589
MGI:3055913	M	MP:0005578	teratozoospermia	Nectin2<tm1Vrr>/Nectin2<tm1Vrr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10733589
MGI:3055950	M	MP:0005669	increased circulating leptin level	Tg(SLC2A4-OGT)15Jaha/0	involves: C57BL/6	N	12136128
MGI:3055950	M	MP:0005331	insulin resistance	Tg(SLC2A4-OGT)15Jaha/0	involves: C57BL/6	N	12136128
MGI:3055970	F	MP:0005551	abnormal eye electrophysiology	Nyx<nob>/Nyx<nob>	BALB/c-Nyx<nob>	N	9804152
MGI:3055970	F	MP:0002090	abnormal vision	Nyx<nob>/Nyx<nob>	BALB/c-Nyx<nob>	N	12506099
MGI:3055970	F	MP:0004022	abnormal cone electrophysiology	Nyx<nob>/Nyx<nob>	BALB/c-Nyx<nob>	N	9804152
MGI:3055970	F	MP:0004021	abnormal rod electrophysiology	Nyx<nob>/Nyx<nob>	BALB/c-Nyx<nob>	N	9804152
MGI:3055970	F	MP:0010749	absent visual evoked potential	Nyx<nob>/Nyx<nob>	BALB/c-Nyx<nob>	N	9804152
MGI:3056062	M	MP:0001922	reduced male fertility	Btrc<tm1Paga>/Btrc<tm1Paga>	involves: 129S2/SvPas	N	12791266
MGI:3056062	M	MP:0002687	oligozoospermia	Btrc<tm1Paga>/Btrc<tm1Paga>	involves: 129S2/SvPas	N	12791266
MGI:3056062	M	MP:0005169	abnormal male meiosis	Btrc<tm1Paga>/Btrc<tm1Paga>	involves: 129S2/SvPas	N	12791266
MGI:3056102	F	MP:0001882	abnormal lactation	Timp3<tm1Rkho>/Timp3<tm1Rkho>	FVB.129-Timp3<tm1Rkho>	N	11560952
MGI:3056102	F	MP:0006271	abnormal involution of the mammary gland	Timp3<tm1Rkho>/Timp3<tm1Rkho>	FVB.129-Timp3<tm1Rkho>	N	11560952
MGI:3056200	M	MP:0002687	oligozoospermia	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056200	M	MP:0001156	abnormal spermatogenesis	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056200	M	MP:0001784	abnormal fluid regulation	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056200	M	MP:0005578	teratozoospermia	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056200	M	MP:0004929	decreased epididymis weight	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056200	M	MP:0002675	asthenozoospermia	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056200	M	MP:0009140	dilated efferent ductule of testis	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056200	M	MP:0004930	small epididymis	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056200	M	MP:0009234	absent sperm head	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056200	M	MP:0002662	abnormal cauda epididymis morphology	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056200	M	MP:0001148	enlarged testis	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056200	M	MP:0009257	dilated seminiferous tubule	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056200	M	MP:0009237	kinked sperm flagellum	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056200	M	MP:0001922	reduced male fertility	Adgrg2<tm1Bend>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15367682
MGI:3056317	M	MP:0001156	abnormal spermatogenesis	Clcn2<nmf240>/Clcn2<nmf240>	C57BL/6J-Clcn2<nmf240>/J	N	20071672
MGI:3056317	M	MP:0005159	azoospermia	Clcn2<nmf240>/Clcn2<nmf240>	C57BL/6J-Clcn2<nmf240>/J	N	20071672
MGI:3056317	M	MP:0001932	abnormal spermiogenesis	Clcn2<nmf240>/Clcn2<nmf240>	C57BL/6J-Clcn2<nmf240>/J	N	MGI:2651853
MGI:3056342	M	MP:0008518	retina outer nuclear layer degeneration	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	17652759
MGI:3056342	M	MP:0012143	decreased a-wave amplitude	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	17652759
MGI:3056342	M	MP:0008587	short photoreceptor outer segment	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	17652759
MGI:3056342	M	MP:0005551	abnormal eye electrophysiology	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	15326152
MGI:3056342	M	MP:0003728	abnormal retina photoreceptor layer morphology	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	17652759
MGI:3056342	M	MP:0008520	disorganized retina outer plexiform layer	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	17652759
MGI:3056342	M	MP:0008516	disorganized retina outer nuclear layer	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	17652759
MGI:3056342	M	MP:0008586	disorganized photoreceptor outer segment	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	17652759
MGI:3056342	M	MP:0012029	abnormal electroretinogram waveform feature	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	17652759
MGI:3056342	M	MP:0008512	disorganized retina inner nuclear layer	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	17652759
MGI:3056342	M	MP:0001325	abnormal retina morphology	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	15326152
MGI:3056342	M	MP:0008581	disorganized photoreceptor inner segment	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	17652759
MGI:3056342	M	MP:0006069	abnormal retina neuronal layer morphology	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	15326152
MGI:3056342	M	MP:0012144	decreased b-wave amplitude	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	17652759
MGI:3056342	M	MP:0001328	disorganized retina layers	Rs1<tm1Sie>/Y	involves: 129S/SvEv * C57BL/6J	N	15326152
MGI:3056343	F	MP:0005551	abnormal eye electrophysiology	Rs1<tm1Sie>/Rs1<tm1Sie>	involves: 129S/SvEv * C57BL/6J	N	15326152
MGI:3056541	F	MP:0001923	reduced female fertility	Slc30a1<tm1Gka>/Slc30a1<+>	either: (involves: 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * CD-1)	N	15452870
MGI:3056551	F	MP:0002783	abnormal ovary secretion	Ptgfr<tm1Sna>/Ptgfr<tm1Sna>	involves: 129P2/OlaHsd * C57BL/6	N	9235889
MGI:3056551	F	MP:0012010	parturition failure	Ptgfr<tm1Sna>/Ptgfr<tm1Sna>	involves: 129P2/OlaHsd * C57BL/6	N	9235889
MGI:3056551	F	MP:0012010	parturition failure	Ptgfr<tm1Sna>/Ptgfr<tm1Sna>	involves: 129P2/OlaHsd * C57BL/6	N	12606450
MGI:3056653	M	MP:0000715	decreased thymocyte number	Igbp1<tm1Cbt>/Y,Tg(Lck-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	15499020
MGI:3056654	F	MP:0000715	decreased thymocyte number	Igbp1<tm1Cbt>/Igbp1<+>,Tg(Lck-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	15499020
MGI:3056896	F	MP:0001923	reduced female fertility	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	N	11682618
MGI:3056896	M	MP:0004852	decreased testis weight	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	N	11682618
MGI:3057014	F	MP:0000585	kinked tail	Zic3<Ka>/Zic3<+>	involves: BALB/cOlaHsd * C3H/HeH	N	15384171
MGI:3057015	F	MP:0001706	abnormal left-right axis patterning	Zic3<Ka>/Zic3<Ka>	involves: BALB/cOlaHsd * C3H/HeH	N	15384171
MGI:3057015	F	MP:0000269	abnormal heart looping	Zic3<Ka>/Zic3<Ka>	involves: BALB/cOlaHsd * C3H/HeH	N	15384171
MGI:3057306	M	MP:0002216	abnormal seminiferous tubule morphology	Jund<tm1Mya>/Jund<tm1Mya>	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	N	10654608
MGI:3057306	M	MP:0005578	teratozoospermia	Jund<tm1Mya>/Jund<tm1Mya>	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	N	10654608
MGI:3057306	M	MP:0001925	male infertility	Jund<tm1Mya>/Jund<tm1Mya>	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	N	10654608
MGI:3057306	M	MP:0002566	abnormal sexual interaction	Jund<tm1Mya>/Jund<tm1Mya>	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	N	10654608
MGI:3057306	M	MP:0002675	asthenozoospermia	Jund<tm1Mya>/Jund<tm1Mya>	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	N	10654608
MGI:3057306	M	MP:0001156	abnormal spermatogenesis	Jund<tm1Mya>/Jund<tm1Mya>	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	N	10654608
MGI:3057306	M	MP:0002687	oligozoospermia	Jund<tm1Mya>/Jund<tm1Mya>	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	N	10654608
MGI:3057318	F	MP:0001923	reduced female fertility	Dppa3<tm1Dcp>/Dppa3<tm1Dcp>	involves: 129S4/SvJae * C57BL/6J	N	15018652
MGI:3057322	F	MP:0002637	small uterus	Nhlh2<tm1Thbr>/Nhlh2<tm1Thbr>	involves: 129S4/SvJae	N	15470499
MGI:3057322	F	MP:0001127	small ovary	Nhlh2<tm1Thbr>/Nhlh2<tm1Thbr>	involves: 129S4/SvJae	N	15470499
MGI:3057322	M	MP:0001147	small testis	Nhlh2<tm1Thbr>/Nhlh2<tm1Thbr>	involves: 129S4/SvJae	N	15470499
MGI:3057322	M	MP:0005188	small penis	Nhlh2<tm1Thbr>/Nhlh2<tm1Thbr>	involves: 129S4/SvJae	N	15470499
MGI:3487159	F	MP:0001728	failure of embryo implantation	Psmc3<tm1Aki>/Psmc3<tm1Aki>	involves: 129P2/OlaHsd	N	10945464
MGI:3487161	F	MP:0001728	failure of embryo implantation	Psmc4<tm1Aki>/Psmc4<tm1Aki>	involves: 129P2/OlaHsd	N	10945464
MGI:3487264	M	MP:0001156	abnormal spermatogenesis	Ret<tm3.1(RET)Jmi>/Ret<+>	Not Specified	N	15469971
MGI:3487264	M	MP:0001155	arrest of spermatogenesis	Ret<tm3.1(RET)Jmi>/Ret<+>	Not Specified	N	15469971
MGI:3487264	M	MP:0001154	seminiferous tubule degeneration	Ret<tm3.1(RET)Jmi>/Ret<+>	Not Specified	N	15469971
MGI:3505857	F	MP:0001433	polyphagia	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10698180
MGI:3505857	M	MP:0005317	increased triglyceride level	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10593909
MGI:3505857	F	MP:0001262	decreased body weight	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10698180
MGI:3505857	F	MP:0002727	decreased circulating insulin level	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10698180
MGI:3505857	F	MP:0005668	decreased circulating leptin level	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10698180
MGI:3505857	M	MP:0005668	decreased circulating leptin level	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10593909
MGI:3505857	F	MP:0010025	decreased total body fat amount	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10698180
MGI:3505857	M	MP:0010025	decreased total body fat amount	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10593909
MGI:3505857	F	MP:0005450	abnormal energy expenditure	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10698180
MGI:3505857	M	MP:0001433	polyphagia	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10593909
MGI:3505857	M	MP:0000005	increased brown adipose tissue amount	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10593909
MGI:3505857	F	MP:0001783	decreased white adipose tissue amount	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10698180
MGI:3505857	F	MP:0005560	decreased circulating glucose level	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10698180
MGI:3505857	M	MP:0005560	decreased circulating glucose level	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10593909
MGI:3505857	F	MP:0002644	decreased circulating triglyceride level	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10698180
MGI:3505857	M	MP:0001554	increased circulating free fatty acids level	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10593909
MGI:3505857	F	MP:0001554	increased circulating free fatty acids level	C3<tm1Hrc>/C3<tm1Hrc>	involves: 129/Sv * C57BL/6	N	10698180
MGI:3510236	M	MP:0000116	abnormal tooth development	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0005441	increased urine calcium level	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0011376	abnormal kidney corticomedullary boundary morphology	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0000160	kyphosis	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0001759	increased urine glucose level	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0020406	hyperthreoninuria	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0001762	polyuria	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0011445	abnormal renal protein reabsorption	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0030617	hyperglutaminuria	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0002901	increased urine phosphate level	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0005367	renal/urinary system phenotype	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	11115837
MGI:3510236	M	MP:0011445	abnormal renal protein reabsorption	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12815097
MGI:3510236	M	MP:0030682	hydroxyprolinuria	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0002962	increased urine protein level	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0003311	aminoaciduria	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0020400	cystinuria	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510236	M	MP:0003197	nephrocalcinosis	Clcn5<tm1Gug>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11115837
MGI:3510460	F	MP:0001923	reduced female fertility	Tg(AZIP/F)1Vsn/0	involves: FVB/N	N	9784492
MGI:3510460	M	MP:0001922	reduced male fertility	Tg(AZIP/F)1Vsn/0	involves: FVB/N	N	9784492
MGI:3510464	F	MP:0001130	abnormal ovarian folliculogenesis	Foxo3<Gt(XAO26)Byg>/Foxo3<Gt(XAO26)Byg>	involves: 129P2/OlaHsd	N	15308101
MGI:3510635	F	MP:0003531	abnormal vagina development	Dh/Dh	Not Specified	N	MGI:48652
MGI:3510635	F	MP:0001144	vagina atresia	Dh/Dh	Not Specified	N	MGI:48652
MGI:3510635	F	MP:0009086	blind uterine horn	Dh/Dh	Not Specified	N	MGI:48652
MGI:3510635	M	MP:0009204	absent external male genitalia	Dh/Dh	Not Specified	N	14444358
MGI:3510737	F	MP:0001134	absent corpus luteum	Cebpb<tm1Pfj>/Cebpb<tm1Pfj>	involves: 129S1/Sv * C57BL/6	N	9303532
MGI:3510737	F	MP:0003357	impaired granulosa cell differentiation	Cebpb<tm1Pfj>/Cebpb<tm1Pfj>	involves: 129S1/Sv * C57BL/6	N	9303532
MGI:3510737	F	MP:0003356	impaired luteinization	Cebpb<tm1Pfj>/Cebpb<tm1Pfj>	involves: 129S1/Sv * C57BL/6	N	9303532
MGI:3510737	F	MP:0001129	impaired ovarian folliculogenesis	Cebpb<tm1Pfj>/Cebpb<tm1Pfj>	involves: 129S1/Sv * C57BL/6	N	9303532
MGI:3510737	F	MP:0001926	female infertility	Cebpb<tm1Pfj>/Cebpb<tm1Pfj>	involves: 129S1/Sv * C57BL/6	N	9303532
MGI:3510737	F	MP:0009009	absent estrous cycle	Cebpb<tm1Pfj>/Cebpb<tm1Pfj>	involves: 129S1/Sv * C57BL/6	N	9303532
MGI:3510737	F	MP:0031420	decreased superovulation rate	Cebpb<tm1Pfj>/Cebpb<tm1Pfj>	involves: 129S1/Sv * C57BL/6	N	9303532
MGI:3510863	F	MP:0000662	abnormal branching of the mammary ductal tree	Cebpb<tm1Pfj>/Cebpb<tm1Pfj>	either: 129S1/SvImJ-Cebpb<tm1Pfj> or (involves: 129S1/SvImJ * C57BL/6)	N	9637691
MGI:3510863	F	MP:0001882	abnormal lactation	Cebpb<tm1Pfj>/Cebpb<tm1Pfj>	either: 129S1/SvImJ-Cebpb<tm1Pfj> or (involves: 129S1/SvImJ * C57BL/6)	N	9637691
MGI:3510863	F	MP:0000628	abnormal mammary gland development	Cebpb<tm1Pfj>/Cebpb<tm1Pfj>	either: 129S1/SvImJ-Cebpb<tm1Pfj> or (involves: 129S1/SvImJ * C57BL/6)	N	9637691
MGI:3511519	M	MP:0002687	oligozoospermia	Hstx1<PWD/Ph>/Y	involves: C57BL/6J * PWD/Ph	N	15366371
MGI:3511519	M	MP:0005578	teratozoospermia	Hstx1<PWD/Ph>/Y	involves: C57BL/6J * PWD/Ph	N	15366371
MGI:3511519	M	MP:0001925	male infertility	Hstx1<PWD/Ph>/Y	involves: C57BL/6J * PWD/Ph	N	15366371
MGI:3511848	F	MP:0002196	absent corpus callosum	Efnb1<tm1.1Sor>/Efnb1<tm1.1Sor>	involves: 129S4/SvJaeSor	N	19515977
MGI:3511848	F	MP:0012752	abnormal cardiac neural crest cell migration	Efnb1<tm1.1Sor>/Efnb1<tm1.1Sor>	involves: 129S4/SvJaeSor	N	15037550
MGI:3511848	F	MP:0000030	abnormal tympanic ring morphology	Efnb1<tm1.1Sor>/Efnb1<tm1.1Sor>	involves: 129S4/SvJaeSor	N	15037550
MGI:3511848	F	MP:0000030	abnormal tympanic ring morphology	Efnb1<tm1.1Sor>/Efnb1<tm1.1Sor>	involves: 129S4/SvJaeSor	N	19515977
MGI:3511848	F	MP:0000150	abnormal rib morphology	Efnb1<tm1.1Sor>/Efnb1<tm1.1Sor>	involves: 129S4/SvJaeSor	N	19515977
MGI:3511848	F	MP:0001081	abnormal cranial ganglia morphology	Efnb1<tm1.1Sor>/Efnb1<tm1.1Sor>	involves: 129S4/SvJaeSor	N	15037550
MGI:3511848	F	MP:0009890	cleft secondary palate	Efnb1<tm1.1Sor>/Efnb1<tm1.1Sor>	involves: 129S4/SvJaeSor	N	15037550
MGI:3511848	F	MP:0012757	abnormal cranial neural crest cell migration	Efnb1<tm1.1Sor>/Efnb1<tm1.1Sor>	involves: 129S4/SvJaeSor	N	15037550
MGI:3511848	F	MP:0009882	absent palatal shelf	Efnb1<tm1.1Sor>/Efnb1<tm1.1Sor>	involves: 129S4/SvJaeSor	N	15037550
MGI:3511848	F	MP:0000780	abnormal corpus callosum morphology	Efnb1<tm1.1Sor>/Efnb1<tm1.1Sor>	involves: 129S4/SvJaeSor	N	19515977
MGI:3511848	F	MP:0009890	cleft secondary palate	Efnb1<tm1.1Sor>/Efnb1<tm1.1Sor>	involves: 129S4/SvJaeSor	N	19515977
MGI:3511848	F	MP:0001061	abnormal oculomotor nerve morphology	Efnb1<tm1.1Sor>/Efnb1<tm1.1Sor>	involves: 129S4/SvJaeSor	N	15037550
MGI:3511851	F	MP:0005404	abnormal axon morphology	Efnb1<tm1.1Sor>/Efnb1<+>	involves: 129S4/SvJaeSor	N	21847105
MGI:3511851	F	MP:0004378	frontal bone foramen	Efnb1<tm1.1Sor>/Efnb1<+>	involves: 129S4/SvJaeSor	N	19515977
MGI:3511851	F	MP:0000562	polydactyly	Efnb1<tm1.1Sor>/Efnb1<+>	involves: 129S4/SvJaeSor	N	19515977
MGI:3511853	F	MP:0011967	increased or absent threshold for auditory brainstem response	tmgc36/tmgc36	C57BL/6-Chr 19<PWK> tmgc36	N	MGI:3053008
MGI:3511855	M	MP:0011967	increased or absent threshold for auditory brainstem response	tmgc37/tmgc37	Mixed stock	N	MGI:3053008
MGI:3511874	F	MP:0005168	abnormal female meiosis	Popoa<LT/SvKau>/?	involves: CAST/Ei * LT/SvKau	N	15509702
MGI:3511874	F	MP:0001928	abnormal ovulation	Popoa<LT/SvKau>/?	involves: CAST/Ei * LT/SvKau	N	15509702
MGI:3511894	M	MP:0001906	increased dopamine level	Maoa<K284stop> Maob<tm1Shih>/Y	either: (involves: 129S/SvEv * 129S6/SvEvTac) or (involves: 129S4/SvJae * 129S6/SvEvTac)	N	15272015
MGI:3511894	M	MP:0001363	increased anxiety-related response	Maoa<K284stop> Maob<tm1Shih>/Y	either: (involves: 129S/SvEv * 129S6/SvEvTac) or (involves: 129S4/SvJae * 129S6/SvEvTac)	N	15272015
MGI:3511894	M	MP:0010069	increased serotonin level	Maoa<K284stop> Maob<tm1Shih>/Y	either: (involves: 129S/SvEv * 129S6/SvEvTac) or (involves: 129S4/SvJae * 129S6/SvEvTac)	N	15272015
MGI:3511894	M	MP:0001417	decreased exploration in new environment	Maoa<K284stop> Maob<tm1Shih>/Y	either: (involves: 129S/SvEv * 129S6/SvEvTac) or (involves: 129S4/SvJae * 129S6/SvEvTac)	N	15272015
MGI:3511894	M	MP:0001353	increased aggression towards mice	Maoa<K284stop> Maob<tm1Shih>/Y	either: (involves: 129S/SvEv * 129S6/SvEvTac) or (involves: 129S4/SvJae * 129S6/SvEvTac)	N	15272015
MGI:3511894	M	MP:0012575	increased noradrenaline level	Maoa<K284stop> Maob<tm1Shih>/Y	either: (involves: 129S/SvEv * 129S6/SvEvTac) or (involves: 129S4/SvJae * 129S6/SvEvTac)	N	15272015
MGI:3511928	F	MP:0006271	abnormal involution of the mammary gland	Il6st<tm1Mam>/Il6st<tm1Mam>,Tg(Wap-cre)11738Mam/0	Not Specified	N	15292206
MGI:3512233	F	MP:0031411	increased ovulation rate	Orq1<M16i>/Orq1<M16i>	involves: L6 * M16i	N	15672592
MGI:3512234	F	MP:0031411	increased ovulation rate	Orq1<L6>/Orq1<M16i>	involves: L6 * M16i	N	15672592
MGI:3512235	F	MP:0031411	increased ovulation rate	Orq3<M16i>/Orq3<M16i>	involves: L6 * M16i	N	15672592
MGI:3512236	F	MP:0031411	increased ovulation rate	Orq3<L6>/Orq3<M16i>	involves: L6 * M16i	N	15672592
MGI:3512452	M	MP:0008152	decreased diameter of femur	Fgf23<tm1Blan>/Fgf23<tm1Blan>,Phex<Hyp>/Y	Not Specified	N	15579309
MGI:3512452	M	MP:0000559	abnormal femur morphology	Fgf23<tm1Blan>/Fgf23<tm1Blan>,Phex<Hyp>/Y	Not Specified	N	15579309
MGI:3512452	M	MP:0004348	long femur	Fgf23<tm1Blan>/Fgf23<tm1Blan>,Phex<Hyp>/Y	Not Specified	N	15579309
MGI:3512452	M	MP:0001566	increased circulating phosphate level	Fgf23<tm1Blan>/Fgf23<tm1Blan>,Phex<Hyp>/Y	Not Specified	N	15579309
MGI:3512452	M	MP:0002896	abnormal bone mineralization	Fgf23<tm1Blan>/Fgf23<tm1Blan>,Phex<Hyp>/Y	Not Specified	N	15579309
MGI:3512461	M	MP:0000133	abnormal long bone metaphysis morphology	Fgf23<tm1Blan>/Fgf23<+>,Phex<Hyp>/Y	Not Specified	N	15579309
MGI:3512461	M	MP:0003109	short femur	Fgf23<tm1Blan>/Fgf23<+>,Phex<Hyp>/Y	Not Specified	N	15579309
MGI:3512461	M	MP:0008158	increased diameter of femur	Fgf23<tm1Blan>/Fgf23<+>,Phex<Hyp>/Y	Not Specified	N	15579309
MGI:3512474	F	MP:0031411	increased ovulation rate	Orq2<L6>/Orq2<M16i>	involves: L6 * M16i	N	15672592
MGI:3512475	F	MP:0031411	increased ovulation rate	Orq2<M16i>/Orq2<M16i>	involves: L6 * M16i	N	15672592
MGI:3512499	M	MP:0002216	abnormal seminiferous tubule morphology	Mhstq1<M. macedonius>/Mhstq1<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512499	M	MP:0001925	male infertility	Mhstq1<M. macedonius>/Mhstq1<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512499	M	MP:0009230	abnormal sperm head morphology	Mhstq1<M. macedonius>/Mhstq1<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512499	M	MP:0001147	small testis	Mhstq1<M. macedonius>/Mhstq1<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512499	M	MP:0008279	arrest of spermiogenesis	Mhstq1<M. macedonius>/Mhstq1<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512499	M	MP:0001169	abnormal bulbourethral gland morphology	Mhstq1<M. macedonius>/Mhstq1<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512499	M	MP:0002717	abnormal male preputial gland morphology	Mhstq1<M. macedonius>/Mhstq1<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512499	M	MP:0008545	absent sperm flagellum	Mhstq1<M. macedonius>/Mhstq1<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512499	M	MP:0004852	decreased testis weight	Mhstq1<M. macedonius>/Mhstq1<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512502	M	MP:0009234	absent sperm head	Mhstq2<M. macedonius>/Mhstq2<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512502	F	MP:0003179	thrombocytopenia	Mhstq2<M. macedonius>/Mhstq2<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512502	M	MP:0009230	abnormal sperm head morphology	Mhstq2<M. macedonius>/Mhstq2<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512502	M	MP:0002216	abnormal seminiferous tubule morphology	Mhstq2<M. macedonius>/Mhstq2<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512502	M	MP:0005159	azoospermia	Mhstq2<M. macedonius>/Mhstq2<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512502	M	MP:0004852	decreased testis weight	Mhstq2<M. macedonius>/Mhstq2<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512502	M	MP:0001925	male infertility	Mhstq2<M. macedonius>/Mhstq2<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512502	M	MP:0001153	small seminiferous tubules	Mhstq2<M. macedonius>/Mhstq2<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512502	M	MP:0005169	abnormal male meiosis	Mhstq2<M. macedonius>/Mhstq2<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512505	M	MP:0005169	abnormal male meiosis	Xydsq<M. macedonius>/Xydsq<M. macedonius>	involves: C57BL/6J * M. macedonius	N	15389318
MGI:3512787	F	MP:0003355	decreased ovulation rate	Wt1<tm1Vih>/Wt1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	24009315
MGI:3512787	F	MP:0001923	reduced female fertility	Wt1<tm1Vih>/Wt1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	24009315
MGI:3512787	F	MP:0001129	impaired ovarian folliculogenesis	Wt1<tm1Vih>/Wt1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	24009315
MGI:3512787	F	MP:0001127	small ovary	Wt1<tm1Vih>/Wt1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	24009315
MGI:3512787	F	MP:0031420	decreased superovulation rate	Wt1<tm1Vih>/Wt1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	24009315
MGI:3512787	F	MP:0008868	abnormal granulosa cell morphology	Wt1<tm1Vih>/Wt1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	24009315
MGI:3512787	F	MP:0009362	abnormal primary ovarian follicle morphology	Wt1<tm1Vih>/Wt1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	24009315
MGI:3512787	F	MP:0003357	impaired granulosa cell differentiation	Wt1<tm1Vih>/Wt1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	24009315
MGI:3512961	F	MP:0001926	female infertility	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3512961	M	MP:0002675	asthenozoospermia	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3512961	M	MP:0001925	male infertility	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3512961	M	MP:0009230	abnormal sperm head morphology	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3512961	F	MP:0001125	abnormal oocyte morphology	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3512961	M	MP:0002686	globozoospermia	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3512961	F	MP:0001926	female infertility	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3512961	M	MP:0002686	globozoospermia	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3512961	M	MP:0009831	abnormal sperm midpiece morphology	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3512961	M	MP:0002675	asthenozoospermia	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3512961	M	MP:0008892	abnormal sperm flagellum morphology	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3512961	M	MP:0005578	teratozoospermia	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3512961	M	MP:0002687	oligozoospermia	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3512961	M	MP:0006362	abnormal male germ cell morphology	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3512961	M	MP:0001932	abnormal spermiogenesis	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3512961	M	MP:0009325	necrospermia	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3512961	M	MP:0001925	male infertility	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3512961	F	MP:0005168	abnormal female meiosis	Brwd1<repro5>/Brwd1<repro5>	involves: C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3512963	M	MP:0002687	oligozoospermia	repro10/repro10	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3512963	M	MP:0002675	asthenozoospermia	repro10/repro10	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3512963	M	MP:0001925	male infertility	repro10/repro10	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3512963	M	MP:0002686	globozoospermia	repro10/repro10	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513136	M	MP:0004852	decreased testis weight	Akap9<repro12>/Akap9<repro12>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513136	M	MP:0001925	male infertility	Akap9<repro12>/Akap9<repro12>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513136	M	MP:0002687	oligozoospermia	Akap9<repro12>/Akap9<repro12>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513136	M	MP:0002686	globozoospermia	Akap9<repro12>/Akap9<repro12>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513136	M	MP:0004910	decreased seminal vesicle weight	Akap9<repro12>/Akap9<repro12>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513136	M	MP:0002216	abnormal seminiferous tubule morphology	Akap9<repro12>/Akap9<repro12>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513146	M	MP:0002686	globozoospermia	repro15/repro15	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513146	M	MP:0001146	abnormal testis morphology	repro15/repro15	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513146	M	MP:0001925	male infertility	repro15/repro15	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513298	M	MP:0005169	abnormal male meiosis	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	N	15515002
MGI:3513298	M	MP:0005169	abnormal male meiosis	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	N	24589552
MGI:3513298	F	MP:0002777	absent ovarian follicles	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	N	15515002
MGI:3513298	M	MP:0009452	abnormal synaptonemal complex	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	N	24589552
MGI:3513298	M	MP:0008261	arrest of male meiosis	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	N	15515002
MGI:3513298	F	MP:0001127	small ovary	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	N	15515002
MGI:3513298	M	MP:0008261	arrest of male meiosis	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	N	24589552
MGI:3513298	M	MP:0001147	small testis	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	N	15515002
MGI:3513298	M	MP:0009451	abnormal chromosomal synapsis	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	N	24589552
MGI:3513313	F	MP:0000662	abnormal branching of the mammary ductal tree	Brca1<tm3Cxd>/Brca1<tm3Cxd>	involves: 129S6/SvEvTac * FVB/N	N	15485917
MGI:3513313	F	MP:0001126	abnormal ovary morphology	Brca1<tm3Cxd>/Brca1<tm3Cxd>	involves: 129S6/SvEvTac * FVB/N	N	15485917
MGI:3513313	F	MP:0002676	uterus hyperplasia	Brca1<tm3Cxd>/Brca1<tm3Cxd>	involves: 129S6/SvEvTac * FVB/N	N	15485917
MGI:3513439	M	MP:0001146	abnormal testis morphology	repro16/repro16	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513439	M	MP:0002675	asthenozoospermia	repro16/repro16	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513439	M	MP:0002686	globozoospermia	repro16/repro16	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513439	M	MP:0001925	male infertility	repro16/repro16	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513439	M	MP:0002687	oligozoospermia	repro16/repro16	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513447	M	MP:0009239	short sperm flagellum	repro17/repro17	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513447	M	MP:0002675	asthenozoospermia	repro17/repro17	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513447	M	MP:0002687	oligozoospermia	repro17/repro17	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513447	M	MP:0001925	male infertility	repro17/repro17	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513447	M	MP:0002686	globozoospermia	repro17/repro17	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513448	M	MP:0009239	short sperm flagellum	repro20/repro20	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513448	M	MP:0002686	globozoospermia	repro20/repro20	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513448	M	MP:0002675	asthenozoospermia	repro20/repro20	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513448	M	MP:0002687	oligozoospermia	repro20/repro20	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513448	M	MP:0004852	decreased testis weight	repro20/repro20	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513448	M	MP:0008545	absent sperm flagellum	repro20/repro20	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513448	M	MP:0001925	male infertility	repro20/repro20	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513450	M	MP:0002687	oligozoospermia	repro21/repro21	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513450	M	MP:0001925	male infertility	repro21/repro21	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513450	M	MP:0020869	immotile sperm	repro21/repro21	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513450	M	MP:0008545	absent sperm flagellum	repro21/repro21	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513450	M	MP:0004852	decreased testis weight	repro21/repro21	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513450	M	MP:0002686	globozoospermia	repro21/repro21	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513450	M	MP:0000242	impaired fertilization	repro21/repro21	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513450	M	MP:0006380	abnormal spermatid morphology	repro21/repro21	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513455	M	MP:0004901	decreased male germ cell number	Mad2l2<repro22>/Mad2l2<repro22>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513455	M	MP:0005159	azoospermia	Mad2l2<repro22>/Mad2l2<repro22>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513455	F	MP:0001926	female infertility	Mad2l2<repro22>/Mad2l2<repro22>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513455	F	MP:0002777	absent ovarian follicles	Mad2l2<repro22>/Mad2l2<repro22>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513455	M	MP:0001925	male infertility	Mad2l2<repro22>/Mad2l2<repro22>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513455	M	MP:0004852	decreased testis weight	Mad2l2<repro22>/Mad2l2<repro22>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513455	F	MP:0001127	small ovary	Mad2l2<repro22>/Mad2l2<repro22>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513455	F	MP:0005431	decreased oocyte number	Mad2l2<repro22>/Mad2l2<repro22>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513455	M	MP:0001155	arrest of spermatogenesis	Mad2l2<repro22>/Mad2l2<repro22>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513474	F	MP:0001926	female infertility	Prl4a1<tm1Soar>/Prl4a1<tm1Soar>	CD-1.Cg-Prlpa<tm1Soar>	N	15545614
MGI:3513475	M	MP:0005159	azoospermia	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513475	M	MP:0001147	small testis	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	19897936
MGI:3513475	M	MP:0004929	decreased epididymis weight	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	19897936
MGI:3513475	M	MP:0001925	male infertility	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	24067652
MGI:3513475	M	MP:0001925	male infertility	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	19897936
MGI:3513475	M	MP:0001925	male infertility	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513475	M	MP:0006380	abnormal spermatid morphology	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	19897936
MGI:3513475	M	MP:0008261	arrest of male meiosis	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513475	M	MP:0004852	decreased testis weight	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	19897936
MGI:3513475	M	MP:0004852	decreased testis weight	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513475	M	MP:0005159	azoospermia	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	19897936
MGI:3513475	M	MP:0004543	abnormal sperm physiology	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	24067652
MGI:3513475	M	MP:0005389	reproductive system phenotype	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	Y	19897936
MGI:3513475	M	MP:0001155	arrest of spermatogenesis	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	19897936
MGI:3513475	M	MP:0006362	abnormal male germ cell morphology	Tdrd12<repro23>/Tdrd12<repro23>	involves: C3HeB/FeJ * C57BL/6J	N	19897936
MGI:3513476	M	MP:0002687	oligozoospermia	repro24/repro24	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513476	M	MP:0002675	asthenozoospermia	repro24/repro24	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513476	M	MP:0002686	globozoospermia	repro24/repro24	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513476	M	MP:0001925	male infertility	repro24/repro24	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513477	F	MP:0001926	female infertility	repro25/repro25	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513478	M	MP:0006380	abnormal spermatid morphology	repro26/repro26	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513478	M	MP:0000242	impaired fertilization	repro26/repro26	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513478	M	MP:0001925	male infertility	repro26/repro26	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513478	M	MP:0002686	globozoospermia	repro26/repro26	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513478	M	MP:0004852	decreased testis weight	repro26/repro26	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513478	M	MP:0002687	oligozoospermia	repro26/repro26	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513478	M	MP:0008545	absent sperm flagellum	repro26/repro26	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513478	M	MP:0002675	asthenozoospermia	repro26/repro26	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513479	M	MP:0004901	decreased male germ cell number	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	23495255
MGI:3513479	M	MP:0008893	detached sperm flagellum	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	23495255
MGI:3513479	M	MP:0009230	abnormal sperm head morphology	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	23495255
MGI:3513479	M	MP:0005159	azoospermia	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	23495255
MGI:3513479	M	MP:0005578	teratozoospermia	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	23495255
MGI:3513479	M	MP:0001156	abnormal spermatogenesis	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	23495255
MGI:3513479	M	MP:0004852	decreased testis weight	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513479	M	MP:0002687	oligozoospermia	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513479	M	MP:0001932	abnormal spermiogenesis	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	23495255
MGI:3513479	M	MP:0001925	male infertility	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513479	M	MP:0001925	male infertility	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	23495255
MGI:3513479	M	MP:0000242	impaired fertilization	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	23495255
MGI:3513479	M	MP:0009647	decreased fertilization frequency	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	23495255
MGI:3513479	F	MP:0005389	reproductive system phenotype	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	Y	23495255
MGI:3513479	M	MP:0001146	abnormal testis morphology	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	23495255
MGI:3513479	M	MP:0002686	globozoospermia	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513479	M	MP:0002675	asthenozoospermia	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	23495255
MGI:3513479	M	MP:0008280	abnormal male germ cell apoptosis	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	23495255
MGI:3513479	M	MP:0002675	asthenozoospermia	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513479	M	MP:0008545	absent sperm flagellum	Golga3<repro27>/Golga3<repro27>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3513600	M	MP:0001156	abnormal spermatogenesis	Mtmr2<tm1.1Abol>/Mtmr2<tm1.1Abol>	involves: 129S2/SvPas	N	15557122
MGI:3513818	M	MP:0001168	abnormal prostate gland epithelium morphology	Nrtn<tm1Jmi>/Nrtn<tm1Jmi>	involves: 129X1/SvJ * C57BL/6	N	15019945
MGI:3513979	F	MP:0000627	abnormal mammary gland morphology	Lalba<tm1Jvt>/Lalba<tm1Jvt>	involves: 129S2/SvPas * C57BL/6	N	8022817
MGI:3513979	F	MP:0004047	abnormal milk composition	Lalba<tm1Jvt>/Lalba<tm1Jvt>	involves: 129S2/SvPas * C57BL/6	N	8022817
MGI:3513982	F	MP:0004047	abnormal milk composition	Lalba<tm1Jvt>/Lalba<+>	involves: 129S2/SvPas * C57BL/6	N	8022817
MGI:3513982	F	MP:0000627	abnormal mammary gland morphology	Lalba<tm1Jvt>/Lalba<+>	involves: 129S2/SvPas * C57BL/6	N	8022817
MGI:3514129	M	MP:0001147	small testis	Pank2<tm1Jgt>/Pank2<tm1Jgt>	involves: 129X1/SvJ * C57BL/6J	N	15525657
MGI:3514129	M	MP:0005159	azoospermia	Pank2<tm1Jgt>/Pank2<tm1Jgt>	involves: 129X1/SvJ * C57BL/6J	N	15525657
MGI:3514129	M	MP:0001925	male infertility	Pank2<tm1Jgt>/Pank2<tm1Jgt>	involves: 129X1/SvJ * C57BL/6J	N	15525657
MGI:3514129	M	MP:0001155	arrest of spermatogenesis	Pank2<tm1Jgt>/Pank2<tm1Jgt>	involves: 129X1/SvJ * C57BL/6J	N	15525657
MGI:3514129	F	MP:0001923	reduced female fertility	Pank2<tm1Jgt>/Pank2<tm1Jgt>	involves: 129X1/SvJ * C57BL/6J	N	15525657
MGI:3514172	M	MP:0001925	male infertility	Abcg8<tm1Elk>/Abcg8<tm1Elk>	involves: 129S6/SvEvTac * C57BL/6J	N	23180829
MGI:3514172	F	MP:0001926	female infertility	Abcg8<tm1Elk>/Abcg8<tm1Elk>	involves: 129S6/SvEvTac * C57BL/6J	N	23180829
MGI:3521574	F	MP:0009375	thin zona pellucida	Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	Not Specified	N	15509794
MGI:3521574	F	MP:0001923	reduced female fertility	Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	Not Specified	N	15509794
MGI:3521574	F	MP:0001931	abnormal oogenesis	Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	Not Specified	N	15509794
MGI:3521574	F	MP:0003696	abnormal zona pellucida morphology	Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	Not Specified	N	15509794
MGI:3521575	F	MP:0009375	thin zona pellucida	Mgat1<tm2Jxm>/Mgat1<tm1Pst>,Tg(Zp3-cre)1Gwh/0	involves: 129/Sv * C57BL/6 * SJL	N	15509794
MGI:3521575	F	MP:0001931	abnormal oogenesis	Mgat1<tm2Jxm>/Mgat1<tm1Pst>,Tg(Zp3-cre)1Gwh/0	involves: 129/Sv * C57BL/6 * SJL	N	15509794
MGI:3521575	F	MP:0003696	abnormal zona pellucida morphology	Mgat1<tm2Jxm>/Mgat1<tm1Pst>,Tg(Zp3-cre)1Gwh/0	involves: 129/Sv * C57BL/6 * SJL	N	15509794
MGI:3521575	F	MP:0001923	reduced female fertility	Mgat1<tm2Jxm>/Mgat1<tm1Pst>,Tg(Zp3-cre)1Gwh/0	involves: 129/Sv * C57BL/6 * SJL	N	15509794
MGI:3521792	F	MP:0004906	enlarged uterus	Igf2r<tm1Wag>/Igf2r<+>	involves: 129S2/SvPas	N	7984240
MGI:3521792	F	MP:0001144	vagina atresia	Igf2r<tm1Wag>/Igf2r<+>	involves: 129S2/SvPas	N	7984240
MGI:3521901	F	MP:0000630	mammary gland hyperplasia	Sdc1<tm1Cma>/Sdc1<tm1Cma>,Tg(Wnt1)1Hev/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	10888884
MGI:3521990	M	MP:0005159	azoospermia	Agtpbp1<pcd-6J>/Agtpbp1<pcd-6J>	C57BL/6J-Agtpbp1<pcd-6J>/J	N	MGI:2684841
MGI:3521990	M	MP:0003205	testicular atrophy	Agtpbp1<pcd-6J>/Agtpbp1<pcd-6J>	C57BL/6J-Agtpbp1<pcd-6J>/J	N	MGI:2684841
MGI:3522005	M	MP:0001922	reduced male fertility	Del(11Cops3-Rnf112)1Jrl/+	involves: 129S7/SvEvBrd * C57BL/6	N	12724422
MGI:3522005	M	MP:0008892	abnormal sperm flagellum morphology	Del(11Cops3-Rnf112)1Jrl/+	involves: 129S7/SvEvBrd * C57BL/6	N	12724422
MGI:3522005	M	MP:0002687	oligozoospermia	Del(11Cops3-Rnf112)1Jrl/+	involves: 129S7/SvEvBrd * C57BL/6	N	12724422
MGI:3522110	F	MP:0001259	abnormal body weight	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	18367514
MGI:3522110	F	MP:0001923	reduced female fertility	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	18367514
MGI:3522110	F	MP:0001935	decreased litter size	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	18367514
MGI:3522110	F	MP:0008995	early reproductive senescence	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	18367514
MGI:3522110	M	MP:0002717	abnormal male preputial gland morphology	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	12372299
MGI:3522110	F	MP:0008961	abnormal basal metabolism	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	18367514
MGI:3522110	F	MP:0009661	abnormal pregnancy	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	18367514
MGI:3522110	F	MP:0008779	abnormal maternal behavior	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	18367514
MGI:3522110	F	MP:0009009	absent estrous cycle	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	18367514
MGI:3522110	F	MP:0001260	increased body weight	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	18367514
MGI:3522110	F	MP:0001432	abnormal food preference	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	18367514
MGI:3522110	F	MP:0005449	abnormal food intake	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	18367514
MGI:3522110	F	MP:0001385	pup cannibalization	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	18367514
MGI:3522110	F	MP:0009006	prolonged estrous cycle	Per2<tm1Brd>/Per2<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	18367514
MGI:3522138	F	MP:0001923	reduced female fertility	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	15520383
MGI:3522583	M	MP:0001360	abnormal social investigation	Avpr1b<tm1Wsy>/Avpr1b<tm1Wsy>	involves: 129S4/SvJae * C57BL/6	N	12399951
MGI:3522721	M	MP:0002675	asthenozoospermia	Gapdhs<tm1Dao>/Gapdhs<tm1Dao>	involves: 129S6/SvEvTac * C57BL/6N	N	15546993
MGI:3522721	M	MP:0001925	male infertility	Gapdhs<tm1Dao>/Gapdhs<tm1Dao>	involves: 129S6/SvEvTac * C57BL/6N	N	15546993
MGI:3524861	F	MP:0012010	parturition failure	Kcnn3<tm1Jpad>/Kcnn3<tm1Jpad>	involves: 129S4/SvJae * C57BL/6	N	10988076
MGI:3524873	M	MP:0011941	increased fluid intake	Ccl3<tm1Unc>/Ccl3<tm1Unc>	B6.129P2-Ccl3<tm1Unc>/J	N	16105698
MGI:3524907	M	MP:0001147	small testis	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	M	MP:0013737	small bulbourethral gland	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	M	MP:0005536	decreased Leydig cell number	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	F	MP:0009363	abnormal tertiary ovarian follicle morphology	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	17350160
MGI:3524907	F	MP:0001127	small ovary	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	M	MP:0008280	abnormal male germ cell apoptosis	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	17350160
MGI:3524907	F	MP:0001926	female infertility	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	17350160
MGI:3524907	F	MP:0001119	abnormal female reproductive system morphology	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	M	MP:0002774	small prostate gland	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	M	MP:0006380	abnormal spermatid morphology	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	17350160
MGI:3524907	F	MP:0002016	ovary cyst	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	M	MP:0005159	azoospermia	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	M	MP:0005159	azoospermia	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	17350160
MGI:3524907	M	MP:0004930	small epididymis	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	M	MP:0001157	small seminal vesicle	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	F	MP:0005431	decreased oocyte number	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	F	MP:0001121	uterus hypoplasia	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	17350160
MGI:3524907	M	MP:0005536	decreased Leydig cell number	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	17350160
MGI:3524907	F	MP:0009009	absent estrous cycle	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	17350160
MGI:3524907	M	MP:0009202	small external male genitalia	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	F	MP:0001132	absent mature ovarian follicles	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	F	MP:0008258	thin endometrium	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	17350160
MGI:3524907	F	MP:0001134	absent corpus luteum	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	M	MP:0013602	abnormal Leydig cell differentiation	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	17350160
MGI:3524907	M	MP:0001925	male infertility	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	17350160
MGI:3524907	F	MP:0001121	uterus hypoplasia	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	M	MP:0001155	arrest of spermatogenesis	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	M	MP:0001145	abnormal male reproductive system morphology	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	F	MP:0003527	small vulva	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	15569941
MGI:3524907	M	MP:0001155	arrest of spermatogenesis	Lhb<tm1Kmr>/Lhb<tm1Kmr>	involves: 129S7/SvEvBrd * C57BL/6J	N	17350160
MGI:3524999	M	MP:0001925	male infertility	Bbs2<tm1Vcs>/Bbs2<tm1Vcs>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	N	15539463
MGI:3524999	M	MP:0008545	absent sperm flagellum	Bbs2<tm1Vcs>/Bbs2<tm1Vcs>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	N	15539463
MGI:3525103	F	MP:0001926	female infertility	Npr2<tm1Gar>/Npr2<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6	N	15572448
MGI:3525103	F	MP:0001127	small ovary	Npr2<tm1Gar>/Npr2<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6	N	15572448
MGI:3525103	F	MP:0009088	thin uterine horn	Npr2<tm1Gar>/Npr2<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6	N	15572448
MGI:3525103	F	MP:0008258	thin endometrium	Npr2<tm1Gar>/Npr2<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6	N	15572448
MGI:3525103	F	MP:0001120	abnormal uterus morphology	Npr2<tm1Gar>/Npr2<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6	N	15572448
MGI:3525103	F	MP:0009009	absent estrous cycle	Npr2<tm1Gar>/Npr2<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6	N	15572448
MGI:3525103	F	MP:0002637	small uterus	Npr2<tm1Gar>/Npr2<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6	N	15572448
MGI:3525103	F	MP:0001134	absent corpus luteum	Npr2<tm1Gar>/Npr2<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6	N	15572448
MGI:3525103	F	MP:0008257	thin myometrium	Npr2<tm1Gar>/Npr2<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6	N	15572448
MGI:3525486	F	MP:0002411	decreased susceptibility to bacterial infection	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: C57BL/6	N	15618213
MGI:3525489	F	MP:0005387	immune system phenotype	Mmp9<tm1Tvu>/Mmp9<tm1Tvu>,Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae * 129S6/SvEvTac	Y	15618213
MGI:3525491	F	MP:0002411	decreased susceptibility to bacterial infection	Mmp7<tm1Lmm>/Mmp7<tm1Lmm>,Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae	N	15618213
MGI:3525494	F	MP:0002411	decreased susceptibility to bacterial infection	Mmp3<tm1Mrl>/Mmp3<tm1Mrl>,Timp1<tm1Pds>/Timp1<tm1Pds>	involves: C57BL/6	N	15618213
MGI:3525497	F	MP:0002411	decreased susceptibility to bacterial infection	Mmp2<tm1Ito>/Mmp2<tm1Ito>,Timp1<tm1Pds>/Timp1<tm1Pds>	either: (involves: 129S4/SvJae) or (involves: C57BL/6)	N	15618213
MGI:3525499	F	MP:0002411	decreased susceptibility to bacterial infection	Mmp12<tm1Sds>/Mmp12<tm1Sds>,Timp1<tm1Pds>/Timp1<tm1Pds>	either: (involves: 129S4/SvJae) or (involves: C57BL/6)	N	15618213
MGI:3525574	F	MP:0005095	decreased T cell proliferation	Was<tm1Sbs>/Was<tm1Sbs>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	N	9697838
MGI:3525574	F	MP:0003179	thrombocytopenia	Was<tm1Sbs>/Was<tm1Sbs>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	N	9697838
MGI:3525574	F	MP:0000219	increased neutrophil cell number	Was<tm1Sbs>/Was<tm1Sbs>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	N	9697838
MGI:3525574	F	MP:0000490	abnormal crypts of Lieberkuhn morphology	Was<tm1Sbs>/Was<tm1Sbs>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	N	9697838
MGI:3525574	F	MP:0005017	decreased B cell number	Was<tm1Sbs>/Was<tm1Sbs>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	N	9697838
MGI:3525574	F	MP:0002006	neoplasm	Was<tm1Sbs>/Was<tm1Sbs>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	Y	9697838
MGI:3525574	F	MP:0002816	colitis	Was<tm1Sbs>/Was<tm1Sbs>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	N	9697838
MGI:3525574	F	MP:0005018	decreased T cell number	Was<tm1Sbs>/Was<tm1Sbs>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	N	9697838
MGI:3525574	F	MP:0005387	immune system phenotype	Was<tm1Sbs>/Was<tm1Sbs>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	Y	9697838
MGI:3525574	F	MP:0000491	crypts of Lieberkuhn abscesses	Was<tm1Sbs>/Was<tm1Sbs>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	N	9697838
MGI:3525574	F	MP:0005016	decreased lymphocyte cell number	Was<tm1Sbs>/Was<tm1Sbs>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	N	9697838
MGI:3525601	F	MP:0003356	impaired luteinization	Gja1<tm4Kwi>/Gja1<tm4Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	15282340
MGI:3525601	F	MP:0001926	female infertility	Gja1<tm4Kwi>/Gja1<tm4Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	15282340
MGI:3525601	F	MP:0001132	absent mature ovarian follicles	Gja1<tm4Kwi>/Gja1<tm4Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	15282340
MGI:3525601	F	MP:0001131	abnormal ovarian follicle morphology	Gja1<tm4Kwi>/Gja1<tm4Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	15282340
MGI:3525601	F	MP:0001134	absent corpus luteum	Gja1<tm4Kwi>/Gja1<tm4Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	15282340
MGI:3525852	F	MP:0001927	abnormal estrous cycle	Mitf<mi-ce>/Mitf<mi-ce>	involves: DBA/2N	N	8776879
MGI:3526059	F	MP:0005178	increased circulating cholesterol level	Obsty5<SM/J>/?	involves: LG/J * SM/J	N	15561968
MGI:3526059	F	MP:0008908	increased total fat pad weight	Obsty5<SM/J>/?	involves: LG/J * SM/J	N	15561968
MGI:3526059	F	MP:0009298	increased mesenteric fat pad weight	Obsty5<SM/J>/?	involves: LG/J * SM/J	N	15561968
MGI:3526059	F	MP:0005669	increased circulating leptin level	Obsty5<SM/J>/?	involves: LG/J * SM/J	N	15561968
MGI:3526127	F	MP:0000662	abnormal branching of the mammary ductal tree	Hoxa9<tm1Mrc>/Hoxa9<tm1Mrc>,Hoxb9<tm1Mrc>/Hoxb9<tm1Mrc>,Hoxd9<tm1Mrc>/Hoxd9<tm1Mrc>	Not Specified	N	9892669
MGI:3526127	F	MP:0003344	mammary gland hypoplasia	Hoxa9<tm1Mrc>/Hoxa9<tm1Mrc>,Hoxb9<tm1Mrc>/Hoxb9<tm1Mrc>,Hoxd9<tm1Mrc>/Hoxd9<tm1Mrc>	Not Specified	N	9892669
MGI:3526127	F	MP:0001882	abnormal lactation	Hoxa9<tm1Mrc>/Hoxa9<tm1Mrc>,Hoxb9<tm1Mrc>/Hoxb9<tm1Mrc>,Hoxd9<tm1Mrc>/Hoxd9<tm1Mrc>	Not Specified	N	9892669
MGI:3526128	F	MP:0001882	abnormal lactation	Hoxa9<tm1Mrc>/Hoxa9<+>,Hoxb9<tm1Mrc>/Hoxb9<tm1Mrc>,Hoxd9<tm1Mrc>/Hoxd9<tm1Mrc>	Not Specified	N	9892669
MGI:3526128	F	MP:0003344	mammary gland hypoplasia	Hoxa9<tm1Mrc>/Hoxa9<+>,Hoxb9<tm1Mrc>/Hoxb9<tm1Mrc>,Hoxd9<tm1Mrc>/Hoxd9<tm1Mrc>	Not Specified	N	9892669
MGI:3526129	F	MP:0003344	mammary gland hypoplasia	Hoxa9<tm1Mrc>/Hoxa9<tm1Mrc>,Hoxb9<tm1Mrc>/Hoxb9<+>,Hoxd9<tm1Mrc>/Hoxd9<tm1Mrc>	Not Specified	N	9892669
MGI:3526129	F	MP:0001882	abnormal lactation	Hoxa9<tm1Mrc>/Hoxa9<tm1Mrc>,Hoxb9<tm1Mrc>/Hoxb9<+>,Hoxd9<tm1Mrc>/Hoxd9<tm1Mrc>	Not Specified	N	9892669
MGI:3526528	M	MP:0003435	herniated seminal vesicle	Plau<tm1Mlg>/Plau<tm1Mlg>	B6.Cg-Plau<tm1Mlg>	N	11760891
MGI:3526566	M	MP:0005018	decreased T cell number	Apex2<tm1Yun>/Y	B6.129S-Apex2<tm1Yun>	N	15319281
MGI:3526566	M	MP:0009674	decreased birth weight	Apex2<tm1Yun>/Y	B6.129S-Apex2<tm1Yun>	N	15319281
MGI:3526566	M	MP:0009335	decreased splenocyte proliferation	Apex2<tm1Yun>/Y	B6.129S-Apex2<tm1Yun>	N	15319281
MGI:3526566	M	MP:0005017	decreased B cell number	Apex2<tm1Yun>/Y	B6.129S-Apex2<tm1Yun>	N	15319281
MGI:3526566	M	MP:0003644	thymus atrophy	Apex2<tm1Yun>/Y	B6.129S-Apex2<tm1Yun>	N	15319281
MGI:3526566	M	MP:0002875	decreased erythrocyte cell number	Apex2<tm1Yun>/Y	B6.129S-Apex2<tm1Yun>	N	15319281
MGI:3526566	M	MP:0002879	increased cellular sensitivity to X-ray irradiation	Apex2<tm1Yun>/Y	B6.129S-Apex2<tm1Yun>	N	15319281
MGI:3526566	M	MP:0000715	decreased thymocyte number	Apex2<tm1Yun>/Y	B6.129S-Apex2<tm1Yun>	N	15319281
MGI:3526566	M	MP:0000221	decreased leukocyte cell number	Apex2<tm1Yun>/Y	B6.129S-Apex2<tm1Yun>	N	15319281
MGI:3526566	M	MP:0001732	postnatal growth retardation	Apex2<tm1Yun>/Y	B6.129S-Apex2<tm1Yun>	N	15319281
MGI:3526735	F	MP:0001923	reduced female fertility	Sod1<tm1Ysh>/Sod1<tm1Ysh>	involves: 129X1/SvJ * C57BL/6	N	9516486
MGI:3527208	F	MP:0000662	abnormal branching of the mammary ductal tree	Foxa1<tm1Gsc>/Foxa1<tm1Gsc>	involves: 129P2/OlaHsd	N	20501593
MGI:3527340	F	MP:0012010	parturition failure	Akr1c18<tm1Jni>/Akr1c18<tm1Jni>	involves: 129P2/OlaHsd * C57BL/6	N	15471942
MGI:3527340	F	MP:0002293	long gestation period	Akr1c18<tm1Jni>/Akr1c18<tm1Jni>	involves: 129P2/OlaHsd * C57BL/6	N	15471942
MGI:3527493	F	MP:0009506	abnormal mammary gland alveolus morphology	Nr3c1<tm2Gsc>/Nr3c1<tm2Gsc>,Tg(Wap-cre)1Gsc/0	involves: 129P2/OlaHsd * FVB/N	N	15471946
MGI:3527493	F	MP:0006269	abnormal mammary gland growth during pregnancy	Nr3c1<tm2Gsc>/Nr3c1<tm2Gsc>,Tg(Wap-cre)1Gsc/0	involves: 129P2/OlaHsd * FVB/N	N	15471946
MGI:3527794	M	MP:0001145	abnormal male reproductive system morphology	Ncoa1<tm1Bwo>/Ncoa1<tm1Bwo>	involves: 129/Sv * C57BL/6	N	9506940
MGI:3527794	M	MP:0002774	small prostate gland	Ncoa1<tm1Bwo>/Ncoa1<tm1Bwo>	involves: 129/Sv * C57BL/6	N	9506940
MGI:3527794	F	MP:0000628	abnormal mammary gland development	Ncoa1<tm1Bwo>/Ncoa1<tm1Bwo>	involves: 129/Sv * C57BL/6	N	9506940
MGI:3527794	F	MP:0003845	abnormal decidualization	Ncoa1<tm1Bwo>/Ncoa1<tm1Bwo>	involves: 129/Sv * C57BL/6	N	9506940
MGI:3527794	F	MP:0001119	abnormal female reproductive system morphology	Ncoa1<tm1Bwo>/Ncoa1<tm1Bwo>	involves: 129/Sv * C57BL/6	N	9506940
MGI:3527794	M	MP:0001147	small testis	Ncoa1<tm1Bwo>/Ncoa1<tm1Bwo>	involves: 129/Sv * C57BL/6	N	9506940
MGI:3528064	F	MP:0002459	abnormal B cell physiology	Was<tm1Sbs>/Was<tm1Sbs>	involves: C57BL/6 * CBA	N	11493455
MGI:3528193	F	MP:0003009	abnormal cytokine secretion	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S/SvEv	N	14645152
MGI:3528193	F	MP:0001541	abnormal osteoclast physiology	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S/SvEv	N	14726392
MGI:3528193	F	MP:0002423	abnormal mast cell physiology	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S/SvEv	N	14645152
MGI:3528193	F	MP:0003091	abnormal cell migration	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S/SvEv	N	12730112
MGI:3528193	F	MP:0002398	abnormal bone marrow cell morphology/development	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S/SvEv	N	12730112
MGI:3528193	F	MP:0000359	abnormal mast cell morphology	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S/SvEv	N	14645152
MGI:3528193	F	MP:0008396	abnormal osteoclast differentiation	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S/SvEv	N	14726392
MGI:3528378	F	MP:0005095	decreased T cell proliferation	Was<tm1Sbs>/Was<tm1Sbs>	involves: BALB/c	N	12807484
MGI:3528378	F	MP:0005387	immune system phenotype	Was<tm1Sbs>/Was<tm1Sbs>	involves: BALB/c	Y	12807484
MGI:3528378	F	MP:0002455	abnormal dendritic cell antigen presentation	Was<tm1Sbs>/Was<tm1Sbs>	involves: BALB/c	N	12807484
MGI:3528379	F	MP:0002444	abnormal T cell physiology	Cblb<tm1Pngr>/Cblb<tm1Pngr>,Was<tm1Sbs>/Was<tm1Sbs>	Not Specified	N	11070165
MGI:3528380	F	MP:0002444	abnormal T cell physiology	Cblb<tm1Pngr>/Cblb<tm1Pngr>,Vav1<tm1Tyb>/Vav1<tm1Tyb>,Was<tm1Sbs>/Was<tm1Sbs>	involves: 129P2/OlaHsd * 129S2/SvPas * 129S6/SvEvTac	N	11070165
MGI:3529670	M	MP:0002786	abnormal Leydig cell morphology	Sult1e1<tm1Song>/Sult1e1<tm1Song>	involves: 129S6/SvEvTac * C57BL/6	N	11713234
MGI:3529670	M	MP:0004852	decreased testis weight	Sult1e1<tm1Song>/Sult1e1<tm1Song>	involves: 129S6/SvEvTac * C57BL/6	N	11713234
MGI:3529670	M	MP:0001146	abnormal testis morphology	Sult1e1<tm1Song>/Sult1e1<tm1Song>	involves: 129S6/SvEvTac * C57BL/6	N	11713234
MGI:3529670	M	MP:0002674	abnormal sperm motility	Sult1e1<tm1Song>/Sult1e1<tm1Song>	involves: 129S6/SvEvTac * C57BL/6	N	11713234
MGI:3529670	F	MP:0001923	reduced female fertility	Sult1e1<tm1Song>/Sult1e1<tm1Song>	involves: 129S6/SvEvTac * C57BL/6	N	11713234
MGI:3529670	M	MP:0004929	decreased epididymis weight	Sult1e1<tm1Song>/Sult1e1<tm1Song>	involves: 129S6/SvEvTac * C57BL/6	N	11713234
MGI:3529670	M	MP:0002216	abnormal seminiferous tubule morphology	Sult1e1<tm1Song>/Sult1e1<tm1Song>	involves: 129S6/SvEvTac * C57BL/6	N	11713234
MGI:3529670	M	MP:0001152	increased Leydig cell number	Sult1e1<tm1Song>/Sult1e1<tm1Song>	involves: 129S6/SvEvTac * C57BL/6	N	11713234
MGI:3529670	M	MP:0004909	increased seminal vesicle weight	Sult1e1<tm1Song>/Sult1e1<tm1Song>	involves: 129S6/SvEvTac * C57BL/6	N	11713234
MGI:3529677	F	MP:0012172	abnormal amniotic fluid composition	Sult1e1<tm1Song>/Sult1e1<tm1Song>	B6.129S6-Sult1e1<tm1Song>	N	15685171
MGI:3529677	F	MP:0001923	reduced female fertility	Sult1e1<tm1Song>/Sult1e1<tm1Song>	B6.129S6-Sult1e1<tm1Song>	N	15685171
MGI:3529677	F	MP:0005182	increased circulating estradiol level	Sult1e1<tm1Song>/Sult1e1<tm1Song>	B6.129S6-Sult1e1<tm1Song>	N	15685171
MGI:3529677	F	MP:0005464	abnormal platelet physiology	Sult1e1<tm1Song>/Sult1e1<tm1Song>	B6.129S6-Sult1e1<tm1Song>	N	15685171
MGI:3529677	F	MP:0020407	abnormal placental thrombosis	Sult1e1<tm1Song>/Sult1e1<tm1Song>	B6.129S6-Sult1e1<tm1Song>	N	15685171
MGI:3529942	M	MP:0000220	increased monocyte cell number	Nba10<NZB>/Nba10<NZB>,X/Yaa	C57BL/6-Nba2 Yaa	N	16493085
MGI:3529942	M	MP:0002723	abnormal immune serum protein physiology	Nba10<NZB>/Nba10<NZB>,X/Yaa	C57BL/6-Nba2 Yaa	N	18606711
MGI:3529942	M	MP:0002743	glomerulonephritis	Nba10<NZB>/Nba10<NZB>,X/Yaa	C57BL/6-Nba2 Yaa	N	15634937
MGI:3529942	M	MP:0002743	glomerulonephritis	Nba10<NZB>/Nba10<NZB>,X/Yaa	C57BL/6-Nba2 Yaa	N	18606711
MGI:3529942	M	MP:0005615	increased susceptibility to type III hypersensitivity reaction	Nba10<NZB>/Nba10<NZB>,X/Yaa	C57BL/6-Nba2 Yaa	N	15634937
MGI:3529942	M	MP:0000220	increased monocyte cell number	Nba10<NZB>/Nba10<NZB>,X/Yaa	C57BL/6-Nba2 Yaa	N	18606711
MGI:3529942	M	MP:0005350	increased susceptibility to autoimmune disorder	Nba10<NZB>/Nba10<NZB>,X/Yaa	C57BL/6-Nba2 Yaa	N	15634937
MGI:3529942	M	MP:0003725	increased autoantibody level	Nba10<NZB>/Nba10<NZB>,X/Yaa	C57BL/6-Nba2 Yaa	N	18606711
MGI:3529942	M	MP:0004829	increased anti-chromatin antibody level	Nba10<NZB>/Nba10<NZB>,X/Yaa	C57BL/6-Nba2 Yaa	N	18606711
MGI:3529942	M	MP:0004794	increased anti-nuclear antigen antibody level	Nba10<NZB>/Nba10<NZB>,X/Yaa	C57BL/6-Nba2 Yaa	N	15634937
MGI:3530074	M	MP:0009703	decreased birth body size	Atrx<tm1Rjg>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	15668733
MGI:3530074	M	MP:0003240	loss of hippocampal neurons	Atrx<tm1Rjg>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	15668733
MGI:3530074	M	MP:0001436	abnormal suckling behavior	Atrx<tm1Rjg>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	15668733
MGI:3530074	M	MP:0000814	absent dentate gyrus	Atrx<tm1Rjg>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	15668733
MGI:3530074	M	MP:0011085	postnatal lethality, complete penetrance	Atrx<tm1Rjg>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	15668733
MGI:3530074	M	MP:0009546	absent gastric milk in neonates	Atrx<tm1Rjg>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	15668733
MGI:3530074	M	MP:0003241	loss of cortex neurons	Atrx<tm1Rjg>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	15668733
MGI:3530074	M	MP:0009971	decreased hippocampus pyramidal cell number	Atrx<tm1Rjg>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	15668733
MGI:3530076	M	MP:0003240	loss of hippocampal neurons	Atrx<tm1Rjg>/Y,Tg(Nes-cre)2472Pick/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	15668733
MGI:3530076	M	MP:0003241	loss of cortex neurons	Atrx<tm1Rjg>/Y,Tg(Nes-cre)2472Pick/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	15668733
MGI:3530076	M	MP:0009703	decreased birth body size	Atrx<tm1Rjg>/Y,Tg(Nes-cre)2472Pick/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	15668733
MGI:3530076	M	MP:0011086	postnatal lethality, incomplete penetrance	Atrx<tm1Rjg>/Y,Tg(Nes-cre)2472Pick/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	15668733
MGI:3530234	F	MP:0001926	female infertility	Tg(HDexon1)62Gpb/0	involves: C57BL/6J * CBA/J	N	8898202
MGI:3530234	F	MP:0001119	abnormal female reproductive system morphology	Tg(HDexon1)62Gpb/0	involves: C57BL/6J * CBA/J	N	8898202
MGI:3530234	M	MP:0001147	small testis	Tg(HDexon1)62Gpb/0	involves: C57BL/6J * CBA/J	N	8898202
MGI:3530234	F	MP:0001127	small ovary	Tg(HDexon1)62Gpb/0	involves: C57BL/6J * CBA/J	N	8898202
MGI:3530234	F	MP:0002637	small uterus	Tg(HDexon1)62Gpb/0	involves: C57BL/6J * CBA/J	N	8898202
MGI:3530234	M	MP:0001157	small seminal vesicle	Tg(HDexon1)62Gpb/0	involves: C57BL/6J * CBA/J	N	8898202
MGI:3530365	M	MP:0000527	abnormal kidney development	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0003675	kidney cyst	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0005630	increased lung weight	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0003014	abnormal kidney medulla morphology	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	11180950
MGI:3530365	M	MP:0003014	abnormal kidney medulla morphology	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0000460	mandible hypoplasia	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0002412	increased susceptibility to bacterial infection	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0006032	abnormal ureteric bud morphology	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0005376	homeostasis/metabolism phenotype	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	Y	10402475
MGI:3530365	M	MP:0011085	postnatal lethality, complete penetrance	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0000521	abnormal kidney cortex morphology	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0010981	abnormal branching involved in ureteric bud morphogenesis	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0011086	postnatal lethality, incomplete penetrance	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0003068	enlarged kidney	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0001867	rhinitis	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0004754	abnormal kidney collecting duct morphology	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	11180950
MGI:3530365	M	MP:0001861	lung inflammation	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0002707	abnormal kidney weight	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0001260	increased body weight	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530365	M	MP:0003675	kidney cyst	Gpc3<tm1Fil>/Y	B6.Cg-Gpc3<tm1Fil>	N	11180950
MGI:3530366	F	MP:0006032	abnormal ureteric bud morphology	Gpc3<tm1Fil>/Gpc3<+>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530366	F	MP:0000527	abnormal kidney development	Gpc3<tm1Fil>/Gpc3<+>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530366	F	MP:0003675	kidney cyst	Gpc3<tm1Fil>/Gpc3<+>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530366	F	MP:0001260	increased body weight	Gpc3<tm1Fil>/Gpc3<+>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530366	F	MP:0004936	impaired branching involved in ureteric bud morphogenesis	Gpc3<tm1Fil>/Gpc3<+>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3530443	F	MP:0006269	abnormal mammary gland growth during pregnancy	Nrg1<tm1Fej>/Nrg1<tm1Fej>	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	12118369
MGI:3530624	F	MP:0005390	skeleton phenotype	Tnmd<tm1Ref>/Tnmd<tm1Ref>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	15632070
MGI:3530624	F	MP:0005503	abnormal tendon morphology	Tnmd<tm1Ref>/Tnmd<tm1Ref>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15632070
MGI:3530624	F	MP:0005391	vision/eye phenotype	Tnmd<tm1Ref>/Tnmd<tm1Ref>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	15632070
MGI:3530626	F	MP:0005391	vision/eye phenotype	Cnmd<tm1Ref>/Cnmd<tm1Ref>,Tnmd<tm1Ref>/Tnmd<tm1Ref>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	15632070
MGI:3530658	M	MP:0003642	absent seminal vesicle	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	F	MP:0004856	decreased ovary weight	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	F	MP:0001132	absent mature ovarian follicles	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	F	MP:0001143	constricted vagina orifice	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	M	MP:0006380	abnormal spermatid morphology	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	F	MP:0001134	absent corpus luteum	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	M	MP:0001155	arrest of spermatogenesis	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	F	MP:0002637	small uterus	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	M	MP:0001147	small testis	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	F	MP:0001127	small ovary	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	F	MP:0000662	abnormal branching of the mammary ductal tree	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	M	MP:0005159	azoospermia	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	M	MP:0008261	arrest of male meiosis	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	M	MP:0006401	absent male preputial gland	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	F	MP:0009009	absent estrous cycle	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	M	MP:0004852	decreased testis weight	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	M	MP:0001380	reduced male mating frequency	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	M	MP:0001159	absent prostate gland	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	F	MP:0001926	female infertility	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	F	MP:0001121	uterus hypoplasia	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3530658	F	MP:0008869	anovulation	Kiss1r<tm1Coll>/Kiss1r<tm1Coll>	involves: 129S6/SvEvTac	N	14573733
MGI:3531312	M	MP:0002675	asthenozoospermia	Slc9c1<tm1Gar>/Slc9c1<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6J	N	14634667
MGI:3531312	M	MP:0001925	male infertility	Slc9c1<tm1Gar>/Slc9c1<tm1Gar>	involves: 129S6/SvEvTac * C57BL/6J	N	14634667
MGI:3531414	M	MP:0002216	abnormal seminiferous tubule morphology	Nkd1<tm1Tko>/Nkd1<tm1Tko>	involves: 129X1/SvJ	N	15546883
MGI:3531414	M	MP:0001147	small testis	Nkd1<tm1Tko>/Nkd1<tm1Tko>	involves: 129X1/SvJ	N	15546883
MGI:3531414	M	MP:0002687	oligozoospermia	Nkd1<tm1Tko>/Nkd1<tm1Tko>	involves: 129X1/SvJ	N	15546883
MGI:3531414	M	MP:0001153	small seminiferous tubules	Nkd1<tm1Tko>/Nkd1<tm1Tko>	involves: 129X1/SvJ	N	15546883
MGI:3531414	M	MP:0001922	reduced male fertility	Nkd1<tm1Tko>/Nkd1<tm1Tko>	involves: 129X1/SvJ	N	15546883
MGI:3573781	F	MP:0002169	no abnormal phenotype detected	Dmd<tm1Khan>/Dmd<tm1Khan>	involves: C57BL/6 * CBA	N	15694376
MGI:3573782	M	MP:0009412	skeletal muscle fiber degeneration	Dmd<tm1.1Khan>/Y	involves: C57BL/6 * CBA	N	15694376
MGI:3573782	M	MP:0009399	increased skeletal muscle fiber size	Dmd<tm1.1Khan>/Y	involves: C57BL/6 * CBA	N	15694376
MGI:3573782	M	MP:0009414	skeletal muscle fiber necrosis	Dmd<tm1.1Khan>/Y	involves: C57BL/6 * CBA	N	15694376
MGI:3573782	M	MP:0001925	male infertility	Dmd<tm1.1Khan>/Y	involves: C57BL/6 * CBA	N	15694376
MGI:3573926	M	MP:0001940	testis hypoplasia	Kit<tm1Hntr>/Kit<tm1Hntr>	either: (involves: 129/Sv * C57BL/6 * DBA/2) or (involves: 129S1)	N	10655061
MGI:3573926	M	MP:0001925	male infertility	Kit<tm1Hntr>/Kit<tm1Hntr>	either: (involves: 129/Sv * C57BL/6 * DBA/2) or (involves: 129S1)	N	10655061
MGI:3573926	M	MP:0001155	arrest of spermatogenesis	Kit<tm1Hntr>/Kit<tm1Hntr>	either: (involves: 129/Sv * C57BL/6 * DBA/2) or (involves: 129S1)	N	10655061
MGI:3573926	M	MP:0002216	abnormal seminiferous tubule morphology	Kit<tm1Hntr>/Kit<tm1Hntr>	either: (involves: 129/Sv * C57BL/6 * DBA/2) or (involves: 129S1)	N	10655061
MGI:3573926	M	MP:0002685	abnormal spermatogonia proliferation	Kit<tm1Hntr>/Kit<tm1Hntr>	either: (involves: 129/Sv * C57BL/6 * DBA/2) or (involves: 129S1)	N	10655061
MGI:3573946	F	MP:0001926	female infertility	Kit<Wads>/Kit<Wads>	C57BL/6J-Kit<Wads>	N	15731517
MGI:3573946	F	MP:0002777	absent ovarian follicles	Kit<Wads>/Kit<Wads>	C57BL/6J-Kit<Wads>	N	15731517
MGI:3573946	M	MP:0001925	male infertility	Kit<Wads>/Kit<Wads>	C57BL/6J-Kit<Wads>	N	15731517
MGI:3573946	M	MP:0001155	arrest of spermatogenesis	Kit<Wads>/Kit<Wads>	C57BL/6J-Kit<Wads>	N	15731517
MGI:3573946	F	MP:0001127	small ovary	Kit<Wads>/Kit<Wads>	C57BL/6J-Kit<Wads>	N	15731517
MGI:3573946	M	MP:0001147	small testis	Kit<Wads>/Kit<Wads>	C57BL/6J-Kit<Wads>	N	15731517
MGI:3573946	M	MP:0001152	increased Leydig cell number	Kit<Wads>/Kit<Wads>	C57BL/6J-Kit<Wads>	N	15731517
MGI:3573950	F	MP:0001923	reduced female fertility	Zbtb7b<hd>/Zbtb7b<hd>	involves: 129/Sv * BALB/c * C3H * C57BL/6	N	9653162
MGI:3573955	F	MP:0001882	abnormal lactation	Elf5<tm1Mapr>/Elf5<+>	involves: 129S4/SvJae * C57BL/6J	N	15650748
MGI:3573955	F	MP:0000628	abnormal mammary gland development	Elf5<tm1Mapr>/Elf5<+>	involves: 129S4/SvJae * C57BL/6J	N	15650748
MGI:3573956	F	MP:0010249	lactation failure	Elf5<tm1Mapr>/Elf5<+>	involves: 129S4/SvJae * 129T2/SvEms * C57BL/6J	N	15650748
MGI:3574018	M	MP:0006379	abnormal spermatocyte morphology	Dnaja1<tm1Kate>/Dnaja1<tm1Kate>	involves: C57BL/6 * CBA	N	15660130
MGI:3574018	M	MP:0001157	small seminal vesicle	Dnaja1<tm1Kate>/Dnaja1<tm1Kate>	involves: C57BL/6 * CBA	N	15660130
MGI:3574018	M	MP:0002784	abnormal Sertoli cell morphology	Dnaja1<tm1Kate>/Dnaja1<tm1Kate>	involves: C57BL/6 * CBA	N	15660130
MGI:3574018	M	MP:0001147	small testis	Dnaja1<tm1Kate>/Dnaja1<tm1Kate>	involves: C57BL/6 * CBA	N	15660130
MGI:3574018	M	MP:0002687	oligozoospermia	Dnaja1<tm1Kate>/Dnaja1<tm1Kate>	involves: C57BL/6 * CBA	N	15660130
MGI:3574018	M	MP:0001922	reduced male fertility	Dnaja1<tm1Kate>/Dnaja1<tm1Kate>	involves: C57BL/6 * CBA	N	15660130
MGI:3574018	M	MP:0002675	asthenozoospermia	Dnaja1<tm1Kate>/Dnaja1<tm1Kate>	involves: C57BL/6 * CBA	N	15660130
MGI:3574018	M	MP:0006380	abnormal spermatid morphology	Dnaja1<tm1Kate>/Dnaja1<tm1Kate>	involves: C57BL/6 * CBA	N	15660130
MGI:3574018	M	MP:0001154	seminiferous tubule degeneration	Dnaja1<tm1Kate>/Dnaja1<tm1Kate>	involves: C57BL/6 * CBA	N	15660130
MGI:3574458	M	MP:0002675	asthenozoospermia	Septin4<tm1Ksh>/Septin4<tm1Ksh>	involves: 129X1/SvJ * C57BL/6J	N	15737930
MGI:3574458	M	MP:0030590	abnormal sperm fibrous sheath morphology	Septin4<tm1Ksh>/Septin4<tm1Ksh>	involves: 129X1/SvJ * C57BL/6J	N	15737930
MGI:3574458	M	MP:0009835	absent sperm annulus	Septin4<tm1Ksh>/Septin4<tm1Ksh>	involves: 129X1/SvJ * C57BL/6J	N	15737930
MGI:3574458	M	MP:0004543	abnormal sperm physiology	Septin4<tm1Ksh>/Septin4<tm1Ksh>	involves: 129X1/SvJ * C57BL/6J	N	15737930
MGI:3574458	M	MP:0001925	male infertility	Septin4<tm1Ksh>/Septin4<tm1Ksh>	involves: 129X1/SvJ * C57BL/6J	N	15737930
MGI:3574458	M	MP:0009237	kinked sperm flagellum	Septin4<tm1Ksh>/Septin4<tm1Ksh>	involves: 129X1/SvJ * C57BL/6J	N	15737930
MGI:3574521	F	MP:0002052	decreased tumor incidence	Gct4<CAST/Ei>/Gct4<CAST/Ei>	involves: CAST/Ei * SJL * SWR	N	14678975
MGI:3574522	F	MP:0012411	increased granulosa cell tumor incidence	Gct4<SJL/Bm>/Gct4<SJL/Bm>	involves: SJL * SWR	N	14678975
MGI:3574523	F	MP:0012411	increased granulosa cell tumor incidence	Gct4<SJL/Bm>/Gct4<SJL/Bm>,Gct6<SJL>/Gct6<SJL>	involves: CAST/Ei * SJL * SWR	N	14678975
MGI:3574577	F	MP:0004904	increased uterus weight	Phb2<tm1Katz>/Phb2<+>	involves: 129S6/SvEvTac * C57BL/6	N	15713652
MGI:3574577	F	MP:0001120	abnormal uterus morphology	Phb2<tm1Katz>/Phb2<+>	involves: 129S6/SvEvTac * C57BL/6	N	15713652
MGI:3574580	F	MP:0001120	abnormal uterus morphology	Phb2<tm1Katz>/Phb2<+>	129S6/SvEvTac-Bcap37<tm1Katz>	N	15713652
MGI:3574580	F	MP:0004904	increased uterus weight	Phb2<tm1Katz>/Phb2<+>	129S6/SvEvTac-Bcap37<tm1Katz>	N	15713652
MGI:3574636	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(Msmb-TAg)183-2Xuan/0	involves: C57BL/6 * CBA	N	12424611
MGI:3574636	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Msmb-TAg)183-2Xuan/0	involves: C57BL/6 * CBA	N	12424611
MGI:3574636	M	MP:0001167	prostate gland epithelial hyperplasia	Tg(Msmb-TAg)183-2Xuan/0	involves: C57BL/6 * CBA	N	12424611
MGI:3574638	M	MP:0001167	prostate gland epithelial hyperplasia	Tg(Msmb-TAg)186-3Xuan/0	involves: C57BL/6 * CBA	N	12424611
MGI:3574640	M	MP:0002687	oligozoospermia	Adad1<tm1Reb>/Adad1<tm1Reb>	129X1/SvJ-Tenr<tm1Reb>	N	15649457
MGI:3574640	M	MP:0002675	asthenozoospermia	Adad1<tm1Reb>/Adad1<tm1Reb>	129X1/SvJ-Tenr<tm1Reb>	N	15649457
MGI:3574640	M	MP:0001925	male infertility	Adad1<tm1Reb>/Adad1<tm1Reb>	129X1/SvJ-Tenr<tm1Reb>	N	15649457
MGI:3574640	M	MP:0005578	teratozoospermia	Adad1<tm1Reb>/Adad1<tm1Reb>	129X1/SvJ-Tenr<tm1Reb>	N	15649457
MGI:3574641	M	MP:0001925	male infertility	Adad1<tm1Reb>/Adad1<tm1Reb>	involves: 129X1/SvJ * C57BL/6	N	15649457
MGI:3574644	M	MP:0011486	ectopic ureter	Spry1<tm1Jdli>/Spry1<tm1Jdli>,Tg(Hoxb7-cre)13Amc/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15691764
MGI:3574645	M	MP:0011486	ectopic ureter	Spry1<tm1.1Jdli>/Spry1<tm1.1Jdli>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	N	15691764
MGI:3574645	F	MP:0011797	blind ureter	Spry1<tm1.1Jdli>/Spry1<tm1.1Jdli>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	N	15691764
MGI:3574653	M	MP:0009739	enlarged prostate gland dorsolateral lobe	Msmb<tm1Xuan>/Msmb<tm1Xuan>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	15674347
MGI:3574653	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Msmb<tm1Xuan>/Msmb<tm1Xuan>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	15674347
MGI:3574653	M	MP:0031357	enlarged prostate gland ventral lobe	Msmb<tm1Xuan>/Msmb<tm1Xuan>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	15674347
MGI:3574653	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Msmb<tm1Xuan>/Msmb<tm1Xuan>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	15674347
MGI:3574662	M	MP:0009835	absent sperm annulus	Septin4<tm1Hs>/Septin4<tm1Hs>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	15737931
MGI:3574662	M	MP:0003666	impaired sperm capacitation	Septin4<tm1Hs>/Septin4<tm1Hs>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	15737931
MGI:3574662	M	MP:0009836	abnormal sperm principal piece morphology	Septin4<tm1Hs>/Septin4<tm1Hs>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	15737931
MGI:3574662	M	MP:0009243	hairpin sperm flagellum	Septin4<tm1Hs>/Septin4<tm1Hs>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	15737931
MGI:3574662	M	MP:0009242	thin sperm flagellum	Septin4<tm1Hs>/Septin4<tm1Hs>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	15737931
MGI:3574662	M	MP:0020869	immotile sperm	Septin4<tm1Hs>/Septin4<tm1Hs>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	15737931
MGI:3574662	M	MP:0001932	abnormal spermiogenesis	Septin4<tm1Hs>/Septin4<tm1Hs>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	15737931
MGI:3574662	M	MP:0030590	abnormal sperm fibrous sheath morphology	Septin4<tm1Hs>/Septin4<tm1Hs>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	15737931
MGI:3574662	M	MP:0001925	male infertility	Septin4<tm1Hs>/Septin4<tm1Hs>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	15737931
MGI:3574662	M	MP:0014465	abnormal sperm mitochondrial morphology	Septin4<tm1Hs>/Septin4<tm1Hs>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	15737931
MGI:3574662	M	MP:0005578	teratozoospermia	Septin4<tm1Hs>/Septin4<tm1Hs>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	15737931
MGI:3574663	M	MP:0009237	kinked sperm flagellum	Septin4<tm1Hs>/Septin4<+>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	15737931
MGI:3574750	F	MP:0001923	reduced female fertility	Adamts1<tm1Mapr>/Adamts1<tm1Mapr>	involves: 129/Sv * C57BL/6	N	14668204
MGI:3574750	F	MP:0003355	decreased ovulation rate	Adamts1<tm1Mapr>/Adamts1<tm1Mapr>	involves: 129/Sv * C57BL/6	N	14668204
MGI:3574752	F	MP:0001382	abnormal nursing	Tbx15<tm1Akis>/Tbx15<tm1Akis>	involves: 129P2/OlaHsd * NMRI	N	15652702
MGI:3574822	F	MP:0001382	abnormal nursing	Fyn<tm1Sor>/Fyn<tm1Sor>,Src<tm1Sor>/Src<+>	involves: 129S7/SvEvBrd	N	7958873
MGI:3574822	F	MP:0001923	reduced female fertility	Fyn<tm1Sor>/Fyn<tm1Sor>,Src<tm1Sor>/Src<+>	involves: 129S7/SvEvBrd	N	7958873
MGI:3574839	F	MP:0001386	abnormal maternal nurturing	Grm1<rcw-2J>/Grm1<rcw-2J>	either: B6(129X1)-Grm1<rcw-2J>/J or B6.129X1 Bax<tm1Sjk>/J-Grm1<rcw-2J>/J	N	MGI:3574375
MGI:3574839	M	MP:0002566	abnormal sexual interaction	Grm1<rcw-2J>/Grm1<rcw-2J>	either: B6(129X1)-Grm1<rcw-2J>/J or B6.129X1 Bax<tm1Sjk>/J-Grm1<rcw-2J>/J	N	MGI:3574375
MGI:3574842	M	MP:0002566	abnormal sexual interaction	Grid2<ho-15J>/Grid2<ho-15J>	C3(Cg)-Grid2<ho-15J>/GrsrJ	N	MGI:3511771
MGI:3574971	M	MP:0000691	enlarged spleen	Foxp3<tm1Ayr>/Y,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	15780990
MGI:3574971	M	MP:0005350	increased susceptibility to autoimmune disorder	Foxp3<tm1Ayr>/Y,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	15780990
MGI:3574971	M	MP:0000702	enlarged lymph nodes	Foxp3<tm1Ayr>/Y,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	15780990
MGI:3574971	M	MP:0001265	decreased body size	Foxp3<tm1Ayr>/Y,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	15780990
MGI:3574971	M	MP:0001194	dermatitis	Foxp3<tm1Ayr>/Y,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	15780990
MGI:3574972	M	MP:0005387	immune system phenotype	Foxp3<tm1.1Ayr>/Y,Rag1<tm1Mom>/Rag1<tm1Mom>,Tg(TcraTcrb)425Cbn/0	Not Specified	Y	15780990
MGI:3574972	M	MP:0002169	no abnormal phenotype detected	Foxp3<tm1.1Ayr>/Y,Rag1<tm1Mom>/Rag1<tm1Mom>,Tg(TcraTcrb)425Cbn/0	Not Specified	N	15780990
MGI:3574973	M	MP:0008261	arrest of male meiosis	Gnrhr<hh>/Gnrhr<hh>	involves: 129S6/SvEvTac * C57BL/6	N	15625238
MGI:3574973	F	MP:0001129	impaired ovarian folliculogenesis	Gnrhr<hh>/Gnrhr<hh>	involves: 129S6/SvEvTac * C57BL/6	N	15625238
MGI:3574973	F	MP:0001134	absent corpus luteum	Gnrhr<hh>/Gnrhr<hh>	involves: 129S6/SvEvTac * C57BL/6	N	15625238
MGI:3574973	F	MP:0011130	absent tertiary ovarian follicles	Gnrhr<hh>/Gnrhr<hh>	involves: 129S6/SvEvTac * C57BL/6	N	15625238
MGI:3574973	F	MP:0001121	uterus hypoplasia	Gnrhr<hh>/Gnrhr<hh>	involves: 129S6/SvEvTac * C57BL/6	N	15625238
MGI:3574973	M	MP:0004852	decreased testis weight	Gnrhr<hh>/Gnrhr<hh>	involves: 129S6/SvEvTac * C57BL/6	N	15625238
MGI:3574973	M	MP:0001157	small seminal vesicle	Gnrhr<hh>/Gnrhr<hh>	involves: 129S6/SvEvTac * C57BL/6	N	15625238
MGI:3574973	M	MP:0002286	cryptorchism	Gnrhr<hh>/Gnrhr<hh>	involves: 129S6/SvEvTac * C57BL/6	N	15625238
MGI:3574973	F	MP:0001127	small ovary	Gnrhr<hh>/Gnrhr<hh>	involves: 129S6/SvEvTac * C57BL/6	N	15625238
MGI:3574973	M	MP:0001145	abnormal male reproductive system morphology	Gnrhr<hh>/Gnrhr<hh>	involves: 129S6/SvEvTac * C57BL/6	N	15625238
MGI:3574973	M	MP:0005188	small penis	Gnrhr<hh>/Gnrhr<hh>	involves: 129S6/SvEvTac * C57BL/6	N	15625238
MGI:3574973	M	MP:0004930	small epididymis	Gnrhr<hh>/Gnrhr<hh>	involves: 129S6/SvEvTac * C57BL/6	N	15625238
MGI:3574973	F	MP:0001119	abnormal female reproductive system morphology	Gnrhr<hh>/Gnrhr<hh>	involves: 129S6/SvEvTac * C57BL/6	N	15625238
MGI:3574978	F	MP:0005387	immune system phenotype	Foxp3<tm2Ayr>/Foxp3<tm2Ayr>	involves: 129S1/Sv * 129X1/SvJ	Y	15780990
MGI:3574978	F	MP:0002169	no abnormal phenotype detected	Foxp3<tm2Ayr>/Foxp3<tm2Ayr>	involves: 129S1/Sv * 129X1/SvJ	N	15780990
MGI:3574980	M	MP:0002169	no abnormal phenotype detected	Foxp3<tm2Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	15780990
MGI:3574980	M	MP:0005387	immune system phenotype	Foxp3<tm2Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	Y	15780990
MGI:3575018	F	MP:0005551	abnormal eye electrophysiology	Pcdh15<av-Jfb>/Pcdh15<av-Jfb>	involves: 129X1/SvJ * C57BL/6	N	16799054
MGI:3575018	F	MP:0012029	abnormal electroretinogram waveform feature	Pcdh15<av-Jfb>/Pcdh15<av-Jfb>	involves: 129X1/SvJ * C57BL/6	N	16799054
MGI:3575018	F	MP:0004021	abnormal rod electrophysiology	Pcdh15<av-Jfb>/Pcdh15<av-Jfb>	involves: 129X1/SvJ * C57BL/6	N	16799054
MGI:3575019	M	MP:0008261	arrest of male meiosis	Dnmt3l<tm1Scot>/Dnmt3l<tm1Scot>	C57BL/6-Dnmt3l<tm1Scot>	N	15753313
MGI:3575019	M	MP:0005159	azoospermia	Dnmt3l<tm1Scot>/Dnmt3l<tm1Scot>	C57BL/6-Dnmt3l<tm1Scot>	N	15753313
MGI:3575019	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Dnmt3l<tm1Scot>/Dnmt3l<tm1Scot>	C57BL/6-Dnmt3l<tm1Scot>	N	15753313
MGI:3575317	F	MP:0001262	decreased body weight	Efna5<tm1Ddmo>/Efna5<tm1Ddmo>	involves: 129S1/Sv * 129X1/SvJ	N	26672804
MGI:3575317	F	MP:0002679	abnormal corpus luteum morphology	Efna5<tm1Ddmo>/Efna5<tm1Ddmo>	involves: 129S1/Sv * 129X1/SvJ	N	26672804
MGI:3575317	F	MP:0001935	decreased litter size	Efna5<tm1Ddmo>/Efna5<tm1Ddmo>	involves: 129S1/Sv * 129X1/SvJ	N	26672804
MGI:3575317	F	MP:0009648	abnormal superovulation	Efna5<tm1Ddmo>/Efna5<tm1Ddmo>	involves: 129S1/Sv * 129X1/SvJ	N	26672804
MGI:3575317	F	MP:0004834	ovary hemorrhage	Efna5<tm1Ddmo>/Efna5<tm1Ddmo>	involves: 129S1/Sv * 129X1/SvJ	N	26672804
MGI:3575317	F	MP:0005389	reproductive system phenotype	Efna5<tm1Ddmo>/Efna5<tm1Ddmo>	involves: 129S1/Sv * 129X1/SvJ	Y	26672804
MGI:3575317	F	MP:0001923	reduced female fertility	Efna5<tm1Ddmo>/Efna5<tm1Ddmo>	involves: 129S1/Sv * 129X1/SvJ	N	26672804
MGI:3575317	F	MP:0011700	increased cumulus expansion	Efna5<tm1Ddmo>/Efna5<tm1Ddmo>	involves: 129S1/Sv * 129X1/SvJ	N	26672804
MGI:3575317	F	MP:0003507	abnormal ovary physiology	Efna5<tm1Ddmo>/Efna5<tm1Ddmo>	involves: 129S1/Sv * 129X1/SvJ	N	26672804
MGI:3575317	F	MP:0009433	polyovular ovarian follicle	Efna5<tm1Ddmo>/Efna5<tm1Ddmo>	involves: 129S1/Sv * 129X1/SvJ	N	26672804
MGI:3575317	F	MP:0031420	decreased superovulation rate	Efna5<tm1Ddmo>/Efna5<tm1Ddmo>	involves: 129S1/Sv * 129X1/SvJ	N	26672804
MGI:3575500	F	MP:0002016	ovary cyst	Brca1<tm2Cxd>/Brca1<tm2Cxd>,Tg(Fshr-cre)1Ldu/0	involves: C57BL/6 * C57BL/6J * DBA/2	N	15797026
MGI:3575515	M	MP:0004852	decreased testis weight	Zfp384<tm1Tnk>/Zfp384<tm1Tnk>	involves: C57BL/6 * CBA	N	15189450
MGI:3575515	M	MP:0002216	abnormal seminiferous tubule morphology	Zfp384<tm1Tnk>/Zfp384<tm1Tnk>	involves: C57BL/6 * CBA	N	15189450
MGI:3575515	M	MP:0001925	male infertility	Zfp384<tm1Tnk>/Zfp384<tm1Tnk>	involves: C57BL/6 * CBA	N	15189450
MGI:3575515	M	MP:0001154	seminiferous tubule degeneration	Zfp384<tm1Tnk>/Zfp384<tm1Tnk>	involves: C57BL/6 * CBA	N	15189450
MGI:3575518	M	MP:0004852	decreased testis weight	Zfp384<tm1Tnk>/Zfp384<+>	involves: C57BL/6 * CBA	N	15189450
MGI:3575532	F	MP:0001120	abnormal uterus morphology	Lif<tm1Cgre>/Lif<tm1Cgre>	involves: MF1	N	15576827
MGI:3575532	F	MP:0009394	increased uterine NK cell number	Lif<tm1Cgre>/Lif<tm1Cgre>	involves: MF1	N	15576827
MGI:3575664	M	MP:0008249	abnormal common lymphocyte progenitor cell morphology	Hmgb3<tm1Dmb>/Y	involves: 129S6/SvEvTac * 129X1/SvJ	N	15358624
MGI:3575664	M	MP:0006410	abnormal common myeloid progenitor cell morphology	Hmgb3<tm1Dmb>/Y	involves: 129S6/SvEvTac * 129X1/SvJ	N	15358624
MGI:3575664	M	MP:0002608	increased hematocrit	Hmgb3<tm1Dmb>/Y	involves: 129S6/SvEvTac * 129X1/SvJ	N	15358624
MGI:3575664	M	MP:0005564	increased hemoglobin content	Hmgb3<tm1Dmb>/Y	involves: 129S6/SvEvTac * 129X1/SvJ	N	15358624
MGI:3575664	M	MP:0002123	abnormal definitive hematopoiesis	Hmgb3<tm1Dmb>/Y	involves: 129S6/SvEvTac * 129X1/SvJ	N	15358624
MGI:3575664	M	MP:0000245	abnormal erythropoiesis	Hmgb3<tm1Dmb>/Y	involves: 129S6/SvEvTac * 129X1/SvJ	N	15358624
MGI:3575664	M	MP:0005460	abnormal leukopoiesis	Hmgb3<tm1Dmb>/Y	involves: 129S6/SvEvTac * 129X1/SvJ	N	15358624
MGI:3575664	M	MP:0003131	increased erythrocyte cell number	Hmgb3<tm1Dmb>/Y	involves: 129S6/SvEvTac * 129X1/SvJ	N	15358624
MGI:3575664	M	MP:0002591	decreased mean corpuscular volume	Hmgb3<tm1Dmb>/Y	involves: 129S6/SvEvTac * 129X1/SvJ	N	15358624
MGI:3575667	M	MP:0002169	no abnormal phenotype detected	Hmgb3<tm2Dmb>/Y	involves: 129S6/SvEvTac * 129X1/SvJ	N	12714519
MGI:3575716	F	MP:0002492	decreased IgE level	Sh2d1a<tm1Lyin>/Sh2d1a<tm1Lyin>	involves: 129S2/SvPas * C57BL/6	N	12966553
MGI:3575716	F	MP:0001790	abnormal immune system physiology	Sh2d1a<tm1Lyin>/Sh2d1a<tm1Lyin>	involves: 129S2/SvPas * C57BL/6	N	12966553
MGI:3575716	F	MP:0002499	chronic inflammation	Sh2d1a<tm1Lyin>/Sh2d1a<tm1Lyin>	involves: 129S2/SvPas * C57BL/6	N	12966553
MGI:3575716	F	MP:0001805	decreased IgG level	Sh2d1a<tm1Lyin>/Sh2d1a<tm1Lyin>	involves: 129S2/SvPas * C57BL/6	N	12966553
MGI:3575716	F	MP:0008078	increased CD8-positive, alpha-beta T cell number	Sh2d1a<tm1Lyin>/Sh2d1a<tm1Lyin>	involves: 129S2/SvPas * C57BL/6	N	12966553
MGI:3575716	F	MP:0002460	decreased immunoglobulin level	Sh2d1a<tm1Lyin>/Sh2d1a<tm1Lyin>	involves: 129S2/SvPas * C57BL/6	N	12966553
MGI:3575735	F	MP:0011121	decreased primordial ovarian follicle number	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	N	15764706
MGI:3575735	M	MP:0001156	abnormal spermatogenesis	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	N	15764706
MGI:3575735	M	MP:0014162	decreased circulating cortisol level	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	N	15764706
MGI:3575735	M	MP:0003830	abnormal testis development	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	N	15764706
MGI:3575735	F	MP:0003582	abnormal ovary development	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	N	15764706
MGI:3575898	F	MP:0005168	abnormal female meiosis	Smc1b<tm1Jess>/Smc1b<tm1Jess>	involves: 129S6/SvEvTac * C57BL/6	N	15146193
MGI:3575898	M	MP:0008261	arrest of male meiosis	Smc1b<tm1Jess>/Smc1b<tm1Jess>	involves: 129S6/SvEvTac * C57BL/6	N	15146193
MGI:3575898	M	MP:0004852	decreased testis weight	Smc1b<tm1Jess>/Smc1b<tm1Jess>	involves: 129S6/SvEvTac * C57BL/6	N	15146193
MGI:3575898	M	MP:0005169	abnormal male meiosis	Smc1b<tm1Jess>/Smc1b<tm1Jess>	involves: 129S6/SvEvTac * C57BL/6	N	15146193
MGI:3575898	M	MP:0005159	azoospermia	Smc1b<tm1Jess>/Smc1b<tm1Jess>	involves: 129S6/SvEvTac * C57BL/6	N	15146193
MGI:3576066	F	MP:0010249	lactation failure	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas	N	15657434
MGI:3576066	F	MP:0006269	abnormal mammary gland growth during pregnancy	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas	N	15657434
MGI:3576493	F	MP:0002038	increased carcinoma incidence	Trp53<tm3.1Glo>/Trp53<+>	B6.129S7-Trp53<tm3.1Glo>	N	23656786
MGI:3576518	M	MP:0001925	male infertility	Izumo1<tm1Osb>/Izumo1<tm1Osb>	involves: 129S2/SvPas * C57BL/6	N	15759005
MGI:3576692	F	MP:0002169	no abnormal phenotype detected	Foxp3<tm1Flv>/Foxp3<+>	involves: C57BL/6	N	15795373
MGI:3576734	F	MP:0001806	decreased IgM level	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	B6.129S4-Sh2d1a<tm1Cpt>	N	15774582
MGI:3576734	F	MP:0008495	decreased IgG1 level	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	B6.129S4-Sh2d1a<tm1Cpt>	N	15774582
MGI:3576734	F	MP:0008041	absent NK T cells	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	B6.129S4-Sh2d1a<tm1Cpt>	N	15749842
MGI:3576734	F	MP:0008040	decreased NK T cell number	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	B6.129S4-Sh2d1a<tm1Cpt>	N	15749842
MGI:3576734	F	MP:0008190	decreased transitional stage B cell number	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	B6.129S4-Sh2d1a<tm1Cpt>	N	15749842
MGI:3576734	F	MP:0001800	abnormal humoral immune response	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	B6.129S4-Sh2d1a<tm1Cpt>	N	15774582
MGI:3576734	F	MP:0005014	increased B cell number	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	B6.129S4-Sh2d1a<tm1Cpt>	N	15774582
MGI:3576734	F	MP:0008500	increased IgG2a level	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	B6.129S4-Sh2d1a<tm1Cpt>	N	15774582
MGI:3576735	F	MP:0008482	decreased spleen germinal center number	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	C.129S4-Sh2d1a<tm1Cpt>	N	15774582
MGI:3576735	F	MP:0001806	decreased IgM level	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	C.129S4-Sh2d1a<tm1Cpt>	N	15774582
MGI:3576735	F	MP:0001805	decreased IgG level	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	C.129S4-Sh2d1a<tm1Cpt>	N	15774582
MGI:3576739	F	MP:0003009	abnormal cytokine secretion	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * C57BL/6	N	11323694
MGI:3576739	F	MP:0008042	abnormal NK T cell physiology	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * C57BL/6	N	22613797
MGI:3576739	F	MP:0001800	abnormal humoral immune response	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * C57BL/6	N	22613797
MGI:3576739	F	MP:0002490	abnormal immunoglobulin level	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * C57BL/6	N	22613797
MGI:3576739	F	MP:0008192	abnormal germinal center B cell physiology	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * C57BL/6	N	22613797
MGI:3576739	F	MP:0020913	increased susceptibility to Riboviria infection	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * C57BL/6	N	11323694
MGI:3576739	F	MP:0005348	increased T cell proliferation	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * C57BL/6	N	11323694
MGI:3576739	F	MP:0008040	decreased NK T cell number	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * C57BL/6	N	22613797
MGI:3576740	F	MP:0008040	decreased NK T cell number	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * BALB/c	N	22613797
MGI:3576740	F	MP:0002492	decreased IgE level	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * BALB/c	N	11323694
MGI:3576740	F	MP:0005026	decreased susceptibility to parasitic infection	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * BALB/c	N	11323694
MGI:3576740	F	MP:0005387	immune system phenotype	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * BALB/c	Y	22613797
MGI:3576740	F	MP:0003009	abnormal cytokine secretion	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * BALB/c	N	11323694
MGI:3576740	F	MP:0008178	decreased germinal center B cell number	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * BALB/c	N	22613797
MGI:3576740	F	MP:0008176	abnormal germinal center B cell morphology	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * BALB/c	N	22613797
MGI:3576740	F	MP:0001805	decreased IgG level	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae * BALB/c	N	22613797
MGI:3576751	F	MP:0005348	increased T cell proliferation	Sh2d1a<tm1Cpt>/Sh2d1a<+>	involves: 129S4/SvJae * C57BL/6	N	11323694
MGI:3576751	F	MP:0003009	abnormal cytokine secretion	Sh2d1a<tm1Cpt>/Sh2d1a<+>	involves: 129S4/SvJae * C57BL/6	N	11323694
MGI:3576898	F	MP:0002830	gallstones	Lith4<PERA/EiJ>/Lith4<PERA/EiJ>	involves: DBA/2J * PERA/EiJ	N	16151694
MGI:3576899	F	MP:0002830	gallstones	Lith4<DBA/2J>/Lith4<PERA/EiJ>	involves: DBA/2J * PERA/EiJ	N	16151694
MGI:3577313	F	MP:0002169	no abnormal phenotype detected	Vegfd<tm1Mach>/Vegfd<tm1Mach>	involves: 129S1/Sv	N	15743836
MGI:3577404	M	MP:0004852	decreased testis weight	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	M	MP:0005159	azoospermia	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	M	MP:0001152	increased Leydig cell number	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	F	MP:0009070	small oviduct	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	F	MP:0009064	oviduct atrophy	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	M	MP:0001155	arrest of spermatogenesis	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	F	MP:0011125	decreased primary ovarian follicle number	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	M	MP:0001154	seminiferous tubule degeneration	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	M	MP:0014052	increased male germ cell apoptosis	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	M	MP:0001925	male infertility	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	M	MP:0001380	reduced male mating frequency	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	M	MP:0001157	small seminal vesicle	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	M	MP:0013318	abnormal branching involved in seminal vesicle morphogenesis	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	M	MP:0001145	abnormal male reproductive system morphology	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	F	MP:0001923	reduced female fertility	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	F	MP:0004833	ovary atrophy	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	M	MP:0004901	decreased male germ cell number	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	F	MP:0003700	abnormal oviduct transport	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	F	MP:0011121	decreased primordial ovarian follicle number	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577404	F	MP:0001119	abnormal female reproductive system morphology	Safb<tm1So>/Safb<tm1So>	involves: 129 * C57BL/6J	N	15798188
MGI:3577605	M	MP:0002169	no abnormal phenotype detected	Vegfd<tm1Mach>/Y	involves: 129S1/Sv	N	15743836
MGI:3577891	M	MP:0013317	abnormal seminal vesicle development	Bhlha15<tm1Skz>/Bhlha15<tm1Skz>	B6.129S6-Bhlha15<tm1Skz>	N	17901072
MGI:3577891	M	MP:0013903	abnormal seminal vesicle fluid composition	Bhlha15<tm1Skz>/Bhlha15<tm1Skz>	B6.129S6-Bhlha15<tm1Skz>	N	17901072
MGI:3577891	M	MP:0005389	reproductive system phenotype	Bhlha15<tm1Skz>/Bhlha15<tm1Skz>	B6.129S6-Bhlha15<tm1Skz>	Y	17901072
MGI:3577891	M	MP:0013900	seminal vesicle epithelium degeneration	Bhlha15<tm1Skz>/Bhlha15<tm1Skz>	B6.129S6-Bhlha15<tm1Skz>	N	17901072
MGI:3577891	M	MP:0013899	abnormal seminal vesicle epithelium morphology	Bhlha15<tm1Skz>/Bhlha15<tm1Skz>	B6.129S6-Bhlha15<tm1Skz>	N	17901072
MGI:3578098	F	MP:0001881	abnormal mammary gland physiology	Stat5a<tm1Jni>/Stat5a<tm1Jni>	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	N	9630227
MGI:3578098	F	MP:0000662	abnormal branching of the mammary ductal tree	Stat5a<tm1Jni>/Stat5a<tm1Jni>	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	N	9630227
MGI:3578100	F	MP:0001881	abnormal mammary gland physiology	Stat5b<tm1Jni>/Stat5b<tm1Jni>	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	N	9630227
MGI:3578104	F	MP:0002680	decreased corpora lutea number	Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	N	9630227
MGI:3578104	F	MP:0001926	female infertility	Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	N	9630227
MGI:3578357	F	MP:0002016	ovary cyst	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578357	M	MP:0005159	azoospermia	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578357	F	MP:0003696	abnormal zona pellucida morphology	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578357	F	MP:0002679	abnormal corpus luteum morphology	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578357	F	MP:0005431	decreased oocyte number	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578357	F	MP:0001129	impaired ovarian folliculogenesis	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578357	F	MP:0031422	failure of superovulation	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578357	M	MP:0014052	increased male germ cell apoptosis	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578357	M	MP:0001925	male infertility	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578357	F	MP:0001127	small ovary	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578357	M	MP:0001147	small testis	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578357	F	MP:0001926	female infertility	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578357	M	MP:0001155	arrest of spermatogenesis	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578357	F	MP:0001126	abnormal ovary morphology	Ybx2<tm1Nbh>/Ybx2<tm1Nbh>	involves: 129S7/SvEvBrd	N	15824319
MGI:3578510	F	MP:0002169	no abnormal phenotype detected	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>	involves: 129S7/SvEvBrd	N	12444108
MGI:3578511	M	MP:0002169	no abnormal phenotype detected	Arhgap6/Hccs/Mid1<tm1Hzo>/Y	involves: 129S7/SvEvBrd	N	12444108
MGI:3578621	F	MP:0001121	uterus hypoplasia	Lmx1a<dr-2J>/Lmx1a<dr-2J>	involves: AKR/J	N	MGI:62272
MGI:3578630	F	MP:0001386	abnormal maternal nurturing	Mgat5<tm1Jwd>/Mgat5<tm1Jwd>	involves: 129S1/Sv * 129X1/SvJ	N	10700233
MGI:3578662	F	MP:0001923	reduced female fertility	Slc11a2<mk>/Slc11a2<mk>	MK/ReJ	N	5427253
MGI:3578922	F	MP:0001926	female infertility	Zfp36l2<tm1Pjb>/Zfp36l2<tm1Pjb>	either: B6NTac.129-Zfp36l2<tm1Pjb> or (involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ)	N	15342461
MGI:3578926	M	MP:0001154	seminiferous tubule degeneration	B4galnt1<tm1Rlp>/B4galnt1<tm1Rlp>,Hexb<tm1Rlp>/Hexb<tm1Rlp>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	10021458
MGI:3578949	M	MP:0001922	reduced male fertility	Mfge8<Gt(KST227)Byg>/Mfge8<Gt(KST227)Byg>	B6.129P2-Mfge8<Gt(KST227)Byg>	N	15834428
MGI:3579098	M	MP:0002675	asthenozoospermia	Acr<tm1Wen>/Acr<tm1Wen>,H1f1<tm1Drab>/H1f1<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>	involves: 129/Sv * C57BL/6J * CD-1	N	15685642
MGI:3579098	M	MP:0001922	reduced male fertility	Acr<tm1Wen>/Acr<tm1Wen>,H1f1<tm1Drab>/H1f1<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>	involves: 129/Sv * C57BL/6J * CD-1	N	15685642
MGI:3579098	M	MP:0030978	impaired binding of sperm to zona pellucida	Acr<tm1Wen>/Acr<tm1Wen>,H1f1<tm1Drab>/H1f1<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>	involves: 129/Sv * C57BL/6J * CD-1	N	15685642
MGI:3579099	M	MP:0002675	asthenozoospermia	Acr<tm1Wen>/Acr<tm1Wen>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129/Sv * C57BL/6J * CD-1	N	15685642
MGI:3579099	M	MP:0031012	impaired sperm migration in female genital tract	Acr<tm1Wen>/Acr<tm1Wen>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129/Sv * C57BL/6J * CD-1	N	15685642
MGI:3579099	M	MP:0030978	impaired binding of sperm to zona pellucida	Acr<tm1Wen>/Acr<tm1Wen>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129/Sv * C57BL/6J * CD-1	N	15685642
MGI:3579099	M	MP:0001925	male infertility	Acr<tm1Wen>/Acr<tm1Wen>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129/Sv * C57BL/6J * CD-1	N	15685642
MGI:3579100	M	MP:0031012	impaired sperm migration in female genital tract	H1f1<tm1Drab>/H1f1<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129 * C57BL/6J	N	15685642
MGI:3579100	M	MP:0001925	male infertility	H1f1<tm1Drab>/H1f1<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129 * C57BL/6J	N	15685642
MGI:3579100	M	MP:0030976	impaired sperm penetration of zona pellucida	H1f1<tm1Drab>/H1f1<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129 * C57BL/6J	N	15685642
MGI:3579100	M	MP:0002675	asthenozoospermia	H1f1<tm1Drab>/H1f1<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129 * C57BL/6J	N	15685642
MGI:3579101	M	MP:0002675	asthenozoospermia	Acr<tm1Wen>/Acr<tm1Wen>,H1f6<tm1Drab>/H1f6<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>	involves: 129/Sv * C57BL/6J * CD-1	N	15685642
MGI:3579101	M	MP:0001922	reduced male fertility	Acr<tm1Wen>/Acr<tm1Wen>,H1f6<tm1Drab>/H1f6<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>	involves: 129/Sv * C57BL/6J * CD-1	N	15685642
MGI:3579101	M	MP:0030978	impaired binding of sperm to zona pellucida	Acr<tm1Wen>/Acr<tm1Wen>,H1f6<tm1Drab>/H1f6<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>	involves: 129/Sv * C57BL/6J * CD-1	N	15685642
MGI:3579101	M	MP:0031012	impaired sperm migration in female genital tract	Acr<tm1Wen>/Acr<tm1Wen>,H1f6<tm1Drab>/H1f6<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>	involves: 129/Sv * C57BL/6J * CD-1	N	15685642
MGI:3579101	M	MP:0009230	abnormal sperm head morphology	Acr<tm1Wen>/Acr<tm1Wen>,H1f6<tm1Drab>/H1f6<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>	involves: 129/Sv * C57BL/6J * CD-1	N	15685642
MGI:3579102	M	MP:0030976	impaired sperm penetration of zona pellucida	H1f6<tm1Drab>/H1f6<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129 * C57BL/6J	N	15685642
MGI:3579102	M	MP:0001925	male infertility	H1f6<tm1Drab>/H1f6<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129 * C57BL/6J	N	15685642
MGI:3579102	M	MP:0002675	asthenozoospermia	H1f6<tm1Drab>/H1f6<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129 * C57BL/6J	N	15685642
MGI:3579110	M	MP:0001922	reduced male fertility	H1f6<tm1Drab>/H1f6<+>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129 * C57BL/6J	N	15685642
MGI:3579111	M	MP:0001922	reduced male fertility	H1f1<tm1Drab>/H1f1<+>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<tm1Wen>	involves: 129 * C57BL/6J	N	15685642
MGI:3579112	M	MP:0001925	male infertility	H1f1<tm1Drab>/H1f1<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<+>	involves: 129 * C57BL/6J	N	15685642
MGI:3579113	M	MP:0000245	abnormal erythropoiesis	Tg(HBB-Gata1)G4Phi/Y	involves: 129P2/OlaHsd * FVB	N	10952313
MGI:3579113	M	MP:0001577	anemia	Tg(HBB-Gata1)G4Phi/Y	involves: 129P2/OlaHsd * FVB	N	10952313
MGI:3579113	M	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance	Tg(HBB-Gata1)G4Phi/Y	involves: 129P2/OlaHsd * FVB	N	10952313
MGI:3579115	M	MP:0001925	male infertility	H1f6<tm1Drab>/H1f6<tm1Drab>,Smcp<tm1Wen>/Smcp<tm1Wen>,Tnp2<tm1Wen>/Tnp2<+>	involves: 129 * C57BL/6J	N	15685642
MGI:3579119	F	MP:0011099	lethality throughout fetal growth and development, complete penetrance	Gata1<tm1Phi>/Gata1<+>,Tg(HBB-cre)1Phi/0,Tg(HBB-Gata1)G4Phi/0	involves: FVB	N	15175249
MGI:3579119	F	MP:0000245	abnormal erythropoiesis	Gata1<tm1Phi>/Gata1<+>,Tg(HBB-cre)1Phi/0,Tg(HBB-Gata1)G4Phi/0	involves: FVB	N	15175249
MGI:3579119	F	MP:0001577	anemia	Gata1<tm1Phi>/Gata1<+>,Tg(HBB-cre)1Phi/0,Tg(HBB-Gata1)G4Phi/0	involves: FVB	N	15175249
MGI:3579122	M	MP:0001577	anemia	Tg(HBB-Gata1)G4Phi/Y	involves: FVB	N	15175249
MGI:3579122	M	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance	Tg(HBB-Gata1)G4Phi/Y	involves: FVB	N	15175249
MGI:3579122	M	MP:0000245	abnormal erythropoiesis	Tg(HBB-Gata1)G4Phi/Y	involves: FVB	N	15175249
MGI:3579124	F	MP:0000245	abnormal erythropoiesis	Gata1<tm1Phi>/Gata1<+>,Tg(HBB-cre)1Phi/0	involves: FVB	N	15175249
MGI:3579124	F	MP:0001577	anemia	Gata1<tm1Phi>/Gata1<+>,Tg(HBB-cre)1Phi/0	involves: FVB	N	15175249
MGI:3579126	F	MP:0000245	abnormal erythropoiesis	Gata1<tm1Phi>/Gata1<+>,Tg(HBB-Gata1)G4Phi/0	involves: FVB	N	15175249
MGI:3579188	M	MP:0002286	cryptorchism	Gli1<tm1Alj>/Gli1<tm1Alj>,Gli2<tm1Alj>/Gli2<+>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	10725236
MGI:3579188	M	MP:0009199	abnormal external male genitalia morphology	Gli1<tm1Alj>/Gli1<tm1Alj>,Gli2<tm1Alj>/Gli2<+>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	10725236
MGI:3579482	M	MP:0000968	abnormal sensory neuron innervation pattern	Plxna3<tm1Matl>/Y,Plxna4<tm1Matl>/Plxna4<tm1Matl>	either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)	N	15721238
MGI:3579482	M	MP:0001063	abnormal trochlear nerve morphology	Plxna3<tm1Matl>/Y,Plxna4<tm1Matl>/Plxna4<tm1Matl>	either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)	N	15721238
MGI:3579482	M	MP:0002961	abnormal axon guidance	Plxna3<tm1Matl>/Y,Plxna4<tm1Matl>/Plxna4<tm1Matl>	either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)	N	15721238
MGI:3579482	M	MP:0001065	abnormal trigeminal nerve morphology	Plxna3<tm1Matl>/Y,Plxna4<tm1Matl>/Plxna4<tm1Matl>	either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)	N	15721238
MGI:3579500	F	MP:0009352	impaired spacing of implantation sites	Lpar3<tm1Jch>/Lpar3<tm1Jch>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15875025
MGI:3579500	F	MP:0002293	long gestation period	Lpar3<tm1Jch>/Lpar3<tm1Jch>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15875025
MGI:3579500	F	MP:0009649	delayed embryo implantation	Lpar3<tm1Jch>/Lpar3<tm1Jch>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15875025
MGI:3579500	F	MP:0001729	impaired embryo implantation	Lpar3<tm1Jch>/Lpar3<tm1Jch>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15875025
MGI:3579577	M	MP:0001925	male infertility	shmy/shmy	STOCK Ndc1<sks>	N	MGI:69984
MGI:3579642	F	MP:0011121	decreased primordial ovarian follicle number	Alpl<tm1(cre)Nagy>/Alpl<+>,Pou5f1<tm1Scho>/Pou5f1<tm1.1Scho>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	15486564
MGI:3579642	F	MP:0001926	female infertility	Alpl<tm1(cre)Nagy>/Alpl<+>,Pou5f1<tm1Scho>/Pou5f1<tm1.1Scho>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	15486564
MGI:3579642	M	MP:0001152	increased Leydig cell number	Alpl<tm1(cre)Nagy>/Alpl<+>,Pou5f1<tm1Scho>/Pou5f1<tm1.1Scho>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	15486564
MGI:3579642	M	MP:0001153	small seminiferous tubules	Alpl<tm1(cre)Nagy>/Alpl<+>,Pou5f1<tm1Scho>/Pou5f1<tm1.1Scho>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	15486564
MGI:3579642	M	MP:0002687	oligozoospermia	Alpl<tm1(cre)Nagy>/Alpl<+>,Pou5f1<tm1Scho>/Pou5f1<tm1.1Scho>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	15486564
MGI:3579642	M	MP:0001922	reduced male fertility	Alpl<tm1(cre)Nagy>/Alpl<+>,Pou5f1<tm1Scho>/Pou5f1<tm1.1Scho>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	15486564
MGI:3579642	F	MP:0002777	absent ovarian follicles	Alpl<tm1(cre)Nagy>/Alpl<+>,Pou5f1<tm1Scho>/Pou5f1<tm1.1Scho>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	15486564
MGI:3579837	F	MP:0001384	abnormal pup retrieval	Mbd2<tm1Bh>/Mbd2<tm1Bh>	involves: 129P2/OlaHsd * C57BL/6	N	11274056
MGI:3579837	F	MP:0001386	abnormal maternal nurturing	Mbd2<tm1Bh>/Mbd2<tm1Bh>	involves: 129P2/OlaHsd * C57BL/6	N	11274056
MGI:3580003	F	MP:0001923	reduced female fertility	Tg(Crh)227.1Pbl/0	involves: C57BL/6 * SJL	N	1597149
MGI:3580004	F	MP:0001728	failure of embryo implantation	Eomes<tm1Jrt>/Eomes<tm1Jrt>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR)	N	15788452
MGI:3580081	F	MP:0002169	no abnormal phenotype detected	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>	involves: 129S7/SvEvBrd	N	12444108
MGI:3580082	M	MP:0002169	no abnormal phenotype detected	Arhgap6/Hccs/Mid1<tm1Hzo>/Y	involves: 129S7/SvEvBrd	N	12444108
MGI:3580083	F	MP:0002169	no abnormal phenotype detected	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>	involves: 129S7/SvEvBrd	N	12444108
MGI:3580084	M	MP:0002169	no abnormal phenotype detected	Arhgap6/Hccs/Mid1<tm1Hzo>/Y	involves: 129S7/SvEvBrd	N	12444108
MGI:3580085	F	MP:0011091	prenatal lethality, complete penetrance	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580085	F	MP:0001695	abnormal gastrulation	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580085	F	MP:0003984	embryonic growth retardation	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580085	F	MP:0001672	abnormal embryo development	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580086	M	MP:0011091	prenatal lethality, complete penetrance	Arhgap6/Hccs/Mid1<tm1Hzo>/Y,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580086	M	MP:0001695	abnormal gastrulation	Arhgap6/Hccs/Mid1<tm1Hzo>/Y,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580086	M	MP:0001672	abnormal embryo development	Arhgap6/Hccs/Mid1<tm1Hzo>/Y,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580086	M	MP:0003984	embryonic growth retardation	Arhgap6/Hccs/Mid1<tm1Hzo>/Y,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580087	F	MP:0001695	abnormal gastrulation	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580087	F	MP:0001672	abnormal embryo development	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580087	F	MP:0011091	prenatal lethality, complete penetrance	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580087	F	MP:0003984	embryonic growth retardation	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580088	M	MP:0003984	embryonic growth retardation	Arhgap6/Hccs/Mid1<tm1Hzo>/Y,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580088	M	MP:0001672	abnormal embryo development	Arhgap6/Hccs/Mid1<tm1Hzo>/Y,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580088	M	MP:0011091	prenatal lethality, complete penetrance	Arhgap6/Hccs/Mid1<tm1Hzo>/Y,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580088	M	MP:0001695	abnormal gastrulation	Arhgap6/Hccs/Mid1<tm1Hzo>/Y,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580089	F	MP:0003984	embryonic growth retardation	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580089	F	MP:0001695	abnormal gastrulation	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580089	F	MP:0011091	prenatal lethality, complete penetrance	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580089	F	MP:0001672	abnormal embryo development	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580090	M	MP:0003984	embryonic growth retardation	Arhgap6/Hccs/Mid1<tm1Hzo>/Y,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580090	M	MP:0001672	abnormal embryo development	Arhgap6/Hccs/Mid1<tm1Hzo>/Y,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580090	M	MP:0001695	abnormal gastrulation	Arhgap6/Hccs/Mid1<tm1Hzo>/Y,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580090	M	MP:0011091	prenatal lethality, complete penetrance	Arhgap6/Hccs/Mid1<tm1Hzo>/Y,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580091	F	MP:0011091	prenatal lethality, complete penetrance	Arhgap6/Hccs/Mid1<tm1Hzo>/Mid1<+>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580092	F	MP:0011091	prenatal lethality, complete penetrance	Arhgap6/Hccs/Mid1<tm1Hzo>/Hccs<+>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580093	F	MP:0011091	prenatal lethality, complete penetrance	Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6<+>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	12444108
MGI:3580115	M	MP:0001922	reduced male fertility	repro19/repro19	B6;C3Fe-repro19/J	N	MGI:3052828
MGI:3580115	M	MP:0002687	oligozoospermia	repro19/repro19	B6;C3Fe-repro19/J	N	MGI:3052828
MGI:3580115	M	MP:0002674	abnormal sperm motility	repro19/repro19	B6;C3Fe-repro19/J	N	MGI:3052828
MGI:3580115	M	MP:0004852	decreased testis weight	repro19/repro19	B6;C3Fe-repro19/J	N	MGI:3052828
MGI:3580115	M	MP:0004910	decreased seminal vesicle weight	repro19/repro19	B6;C3Fe-repro19/J	N	MGI:3052828
MGI:3580115	M	MP:0005578	teratozoospermia	repro19/repro19	B6;C3Fe-repro19/J	N	MGI:3052828
MGI:3580296	M	MP:0001925	male infertility	Stk11<tm1Keis>/Stk11<tm1Keis>	Not Specified	N	15889149
MGI:3580297	M	MP:0001925	male infertility	Stk11<tm1Keis>/Stk11<tm1Keis>,Tg(Ckmm-cre)5Khn/0	involves: FVB	N	15889149
MGI:3580400	M	MP:0009231	detached acrosome	H1f7<tm1Idvd>/H1f7<tm1Idvd>	Not Specified	N	15710904
MGI:3580400	M	MP:0002675	asthenozoospermia	H1f7<tm1Idvd>/H1f7<tm1Idvd>	Not Specified	N	15710904
MGI:3580400	M	MP:0001922	reduced male fertility	H1f7<tm1Idvd>/H1f7<tm1Idvd>	Not Specified	N	15710904
MGI:3580400	M	MP:0009230	abnormal sperm head morphology	H1f7<tm1Idvd>/H1f7<tm1Idvd>	Not Specified	N	15710904
MGI:3580400	M	MP:0002687	oligozoospermia	H1f7<tm1Idvd>/H1f7<tm1Idvd>	Not Specified	N	15710904
MGI:3580400	M	MP:0001932	abnormal spermiogenesis	H1f7<tm1Idvd>/H1f7<tm1Idvd>	Not Specified	N	15710904
MGI:3580400	M	MP:0009232	abnormal sperm nucleus morphology	H1f7<tm1Idvd>/H1f7<tm1Idvd>	Not Specified	N	15710904
MGI:3580456	F	MP:0001926	female infertility	Prkdc<scid>/Prkdc<scid>,Idua<tm1Clk>/Idua<tm1Clk>	NOD.Cg-Prkdc<scid> Idua<tm1Clk>/J	N	17920451
MGI:3580456	F	MP:0001385	pup cannibalization	Prkdc<scid>/Prkdc<scid>,Idua<tm1Clk>/Idua<tm1Clk>	NOD.Cg-Prkdc<scid> Idua<tm1Clk>/J	N	17920451
MGI:3580494	M	MP:0001145	abnormal male reproductive system morphology	Lhx1<tm1Bhr>/Lhx1<tm1Tmj>	involves: 129S/SvEv * C57BL/6	N	15930111
MGI:3580494	F	MP:0001119	abnormal female reproductive system morphology	Lhx1<tm1Bhr>/Lhx1<tm1Tmj>	involves: 129S/SvEv * C57BL/6	N	15930111
MGI:3580500	F	MP:0003558	absent uterus	Lhx1<tm2.1Bhr>/Lhx1<tm1Tmj>,Tg(Hoxb7-cre)13Amc/0	involves: 129S/SvEv * C57BL/6	N	15930111
MGI:3580500	M	MP:0003557	absent vas deferens	Lhx1<tm2.1Bhr>/Lhx1<tm1Tmj>,Tg(Hoxb7-cre)13Amc/0	involves: 129S/SvEv * C57BL/6	N	15930111
MGI:3580500	F	MP:0001121	uterus hypoplasia	Lhx1<tm2.1Bhr>/Lhx1<tm1Tmj>,Tg(Hoxb7-cre)13Amc/0	involves: 129S/SvEv * C57BL/6	N	15930111
MGI:3580500	M	MP:0004727	absent epididymis	Lhx1<tm2.1Bhr>/Lhx1<tm1Tmj>,Tg(Hoxb7-cre)13Amc/0	involves: 129S/SvEv * C57BL/6	N	15930111
MGI:3580500	F	MP:0011486	ectopic ureter	Lhx1<tm2.1Bhr>/Lhx1<tm1Tmj>,Tg(Hoxb7-cre)13Amc/0	involves: 129S/SvEv * C57BL/6	N	15930111
MGI:3581024	M	MP:0001925	male infertility	Tssk6<tm1Grj>/Tssk6<tm1Grj>	involves: 129 * C57BL/6	N	15870294
MGI:3581024	M	MP:0009230	abnormal sperm head morphology	Tssk6<tm1Grj>/Tssk6<tm1Grj>	involves: 129 * C57BL/6	N	15870294
MGI:3581024	M	MP:0001156	abnormal spermatogenesis	Tssk6<tm1Grj>/Tssk6<tm1Grj>	involves: 129 * C57BL/6	N	15870294
MGI:3581024	M	MP:0002687	oligozoospermia	Tssk6<tm1Grj>/Tssk6<tm1Grj>	involves: 129 * C57BL/6	N	15870294
MGI:3581024	M	MP:0002675	asthenozoospermia	Tssk6<tm1Grj>/Tssk6<tm1Grj>	involves: 129 * C57BL/6	N	15870294
MGI:3581025	M	MP:0002687	oligozoospermia	Tssk6<tm1Grj>/Tssk6<+>	involves: 129 * C57BL/6	N	15870294
MGI:3581145	M	MP:0004542	impaired acrosome reaction	Glra1<spd>/Glra1<spd>	B6C3Fe a/a-Glra1<spd>/J	N	11076688
MGI:3581145	M	MP:0001925	male infertility	Glra1<spd>/Glra1<spd>	B6C3Fe a/a-Glra1<spd>/J	N	3429842
MGI:3581146	M	MP:0004542	impaired acrosome reaction	Glrb<spa>/Glrb<spa>	B6C3Fe a/a-Glrb<spa>/J	N	11076688
MGI:3581148	M	MP:0003642	absent seminal vesicle	Prkdc<scid>/Prkdc<scid>,Gnrh1<hpg>/Gnrh1<hpg>	STOCK Prkdc<scid> Gnrh1<hpg>/Bm	N	7541529
MGI:3581152	M	MP:0013319	seminal vesicle atrophy	Plag1<tm1Wjmv>/Plag1<tm1Wjmv>	involves: 129S1/Sv * 129X1/SvJ * Swiss Webster	N	15606491
MGI:3581152	M	MP:0004910	decreased seminal vesicle weight	Plag1<tm1Wjmv>/Plag1<tm1Wjmv>	involves: 129S1/Sv * 129X1/SvJ * Swiss Webster	N	15606491
MGI:3581152	M	MP:0031362	decreased prostate gland ventral lobe weight	Plag1<tm1Wjmv>/Plag1<tm1Wjmv>	involves: 129S1/Sv * 129X1/SvJ * Swiss Webster	N	15606491
MGI:3581152	M	MP:0002059	abnormal seminal vesicle morphology	Plag1<tm1Wjmv>/Plag1<tm1Wjmv>	involves: 129S1/Sv * 129X1/SvJ * Swiss Webster	N	15606491
MGI:3581152	M	MP:0001922	reduced male fertility	Plag1<tm1Wjmv>/Plag1<tm1Wjmv>	involves: 129S1/Sv * 129X1/SvJ * Swiss Webster	N	15606491
MGI:3581162	F	MP:0001926	female infertility	Hk1<dea>/Hk1<dea>	A/J-Hk1<dea>/J	N	11783948
MGI:3581192	M	MP:0005159	azoospermia	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	N	15937223
MGI:3581192	F	MP:0002777	absent ovarian follicles	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	N	15937223
MGI:3581192	M	MP:0008261	arrest of male meiosis	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	N	15937223
MGI:3581192	F	MP:0004856	decreased ovary weight	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	N	15937223
MGI:3581192	M	MP:0001925	male infertility	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	N	15937223
MGI:3581192	M	MP:0001153	small seminiferous tubules	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	N	15937223
MGI:3581192	M	MP:0001145	abnormal male reproductive system morphology	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	N	15937223
MGI:3581192	F	MP:0001926	female infertility	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	N	15937223
MGI:3581192	F	MP:0001119	abnormal female reproductive system morphology	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	N	15937223
MGI:3581192	M	MP:0004852	decreased testis weight	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	N	15937223
MGI:3581192	M	MP:0005169	abnormal male meiosis	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	N	15937223
MGI:3581208	F	MP:0003356	impaired luteinization	Tshr<hyt>/Tshr<hyt>	CBy.RF-Tshr<hyt>/J	N	11690529
MGI:3581208	F	MP:0031420	decreased superovulation rate	Tshr<hyt>/Tshr<hyt>	CBy.RF-Tshr<hyt>/J	N	11690529
MGI:3581208	F	MP:0005185	decreased circulating progesterone level	Tshr<hyt>/Tshr<hyt>	CBy.RF-Tshr<hyt>/J	N	11690529
MGI:3581208	F	MP:0004014	abnormal uterine environment	Tshr<hyt>/Tshr<hyt>	CBy.RF-Tshr<hyt>/J	N	11690529
MGI:3581208	F	MP:0009009	absent estrous cycle	Tshr<hyt>/Tshr<hyt>	CBy.RF-Tshr<hyt>/J	N	11690529
MGI:3582296	F	MP:0001926	female infertility	Tle5<tm1Grid>/Tle5<tm1Grid>,Runx2<tm1Mjo>/Runx2<+>	involves: 129S1/Sv * C57BL/6	N	15183720
MGI:3582296	M	MP:0001925	male infertility	Tle5<tm1Grid>/Tle5<tm1Grid>,Runx2<tm1Mjo>/Runx2<+>	involves: 129S1/Sv * C57BL/6	N	15183720
MGI:3582320	F	MP:0001923	reduced female fertility	Numbl<tm1Wmz>/Numbl<tm1Wmz>	Not Specified	N	14687546
MGI:3582335	M	MP:0001925	male infertility	Emx1<tm1(cre)Krj>/Emx1<+>,Numb<tm1Ynj>/Numb<tm1Ynj>,Numbl<tm1Wmz>/Numbl<tm1Wmz>	involves: 129S2/SvPas * 129X1/SvJ * CD-1	N	14687546
MGI:3582335	F	MP:0001926	female infertility	Emx1<tm1(cre)Krj>/Emx1<+>,Numb<tm1Ynj>/Numb<tm1Ynj>,Numbl<tm1Wmz>/Numbl<tm1Wmz>	involves: 129S2/SvPas * 129X1/SvJ * CD-1	N	14687546
MGI:3582336	F	MP:0031420	decreased superovulation rate	Oas1d<tm1Zuk>/Oas1d<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	15899864
MGI:3582336	F	MP:0001923	reduced female fertility	Oas1d<tm1Zuk>/Oas1d<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	15899864
MGI:3582336	F	MP:0002680	decreased corpora lutea number	Oas1d<tm1Zuk>/Oas1d<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	15899864
MGI:3582336	F	MP:0001131	abnormal ovarian follicle morphology	Oas1d<tm1Zuk>/Oas1d<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	15899864
MGI:3582492	F	MP:0001923	reduced female fertility	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	N	10983976
MGI:3582492	M	MP:0001922	reduced male fertility	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	N	10983976
MGI:3582498	F	MP:0002169	no abnormal phenotype detected	Morf4l2<tm1.1Kto>/Morf4l2<tm1.1Kto>	involves: 129S7/SvEvBrd * C57BL/6J	N	15923606
MGI:3582499	M	MP:0002169	no abnormal phenotype detected	Morf4l2<tm1.1Kto>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	15923606
MGI:3582501	F	MP:0001698	decreased embryo size	Morf4l1<tm1Kto>/Morf4l1<tm1Kto>,Morf4l2<tm1.1Kto>/Morf4l2<tm1.1Kto>	involves: 129S7/SvEvBrd * C57BL/6J	N	15923606
MGI:3582501	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Morf4l1<tm1Kto>/Morf4l1<tm1Kto>,Morf4l2<tm1.1Kto>/Morf4l2<tm1.1Kto>	involves: 129S7/SvEvBrd * C57BL/6J	N	15923606
MGI:3582503	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Morf4l1<tm1Kto>/Morf4l1<tm1Kto>,Morf4l2<tm1.1Kto>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	15923606
MGI:3582503	M	MP:0001698	decreased embryo size	Morf4l1<tm1Kto>/Morf4l1<tm1Kto>,Morf4l2<tm1.1Kto>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	15923606
MGI:3582524	F	MP:0001127	small ovary	Lipc<tm1Unc>/Lipc<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11906928
MGI:3582524	F	MP:0003355	decreased ovulation rate	Lipc<tm1Unc>/Lipc<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11906928
MGI:3582529	M	MP:0001925	male infertility	Lnpk<Ul>/Lnpk<+>	involves: 101/H * C3H/HeJ	N	MGI:61651
MGI:3582532	M	MP:0001925	male infertility	Lnpk<Ul>/Lnpk<+>	involves: 101/H * C3H/HeJ * C57BL/6J	N	2338491
MGI:3582562	M	MP:0003397	increased muscle weight	X/Tspy-ps<tm1(Mlc3-Gdf8)Mgs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15851664
MGI:3582562	M	MP:0009399	increased skeletal muscle fiber size	X/Tspy-ps<tm1(Mlc3-Gdf8)Mgs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15851664
MGI:3582563	M	MP:0003397	increased muscle weight	X/Tspy-ps<tm2(Mlc3-Gdf8)Mgs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15851664
MGI:3582563	M	MP:0009399	increased skeletal muscle fiber size	X/Tspy-ps<tm2(Mlc3-Gdf8)Mgs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	15851664
MGI:3582580	M	MP:0002216	abnormal seminiferous tubule morphology	Ocln<tm2Sts>/Ocln<tm2Sts>	involves: 129S4/SvJae * C57BL/6	N	11102513
MGI:3582580	M	MP:0001925	male infertility	Ocln<tm2Sts>/Ocln<tm2Sts>	involves: 129S4/SvJae * C57BL/6	N	11102513
MGI:3582580	F	MP:0001382	abnormal nursing	Ocln<tm2Sts>/Ocln<tm2Sts>	involves: 129S4/SvJae * C57BL/6	N	11102513
MGI:3582581	F	MP:0001144	vagina atresia	Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	N	8682293
MGI:3582615	M	MP:0008545	absent sperm flagellum	Mkks<tm1Vcs>/Mkks<tm1Vcs>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	N	15772095
MGI:3582615	F	MP:0020351	decreased vocalization	Mkks<tm1Vcs>/Mkks<tm1Vcs>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	N	15772095
MGI:3582615	M	MP:0001925	male infertility	Mkks<tm1Vcs>/Mkks<tm1Vcs>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	N	15772095
MGI:3582633	M	MP:0001922	reduced male fertility	Sox2<tm1Rlb>/Sox2<+>	involves: 129S/SvEv	N	12514105
MGI:3582634	M	MP:0001147	small testis	Sox2<tm1Rlb>/Sox2<+>	involves: 129S/SvEv * MF1	N	16932809
MGI:3582634	M	MP:0001922	reduced male fertility	Sox2<tm1Rlb>/Sox2<+>	involves: 129S/SvEv * MF1	N	12514105
MGI:3582634	M	MP:0002216	abnormal seminiferous tubule morphology	Sox2<tm1Rlb>/Sox2<+>	involves: 129S/SvEv * MF1	N	16932809
MGI:3582634	M	MP:0002687	oligozoospermia	Sox2<tm1Rlb>/Sox2<+>	involves: 129S/SvEv * MF1	N	16932809
MGI:3582634	M	MP:0001922	reduced male fertility	Sox2<tm1Rlb>/Sox2<+>	involves: 129S/SvEv * MF1	N	16932809
MGI:3582650	F	MP:0001923	reduced female fertility	Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>	involves: 129S2/SvPas * C57BL/6	N	8682294
MGI:3582839	F	MP:0000603	pale liver	Gata1<tm7Sho>/Gata1<tm7Sho>	involves: 129S1/Sv * C57BL/6	N	15895080
MGI:3582839	F	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm7Sho>/Gata1<tm7Sho>	involves: 129S1/Sv * C57BL/6	N	15895080
MGI:3582839	F	MP:0000245	abnormal erythropoiesis	Gata1<tm7Sho>/Gata1<tm7Sho>	involves: 129S1/Sv * C57BL/6	N	15895080
MGI:3582839	F	MP:0000600	liver hypoplasia	Gata1<tm7Sho>/Gata1<tm7Sho>	involves: 129S1/Sv * C57BL/6	N	15895080
MGI:3582840	F	MP:0002417	abnormal megakaryocyte morphology	Gata1<tm8.1Sho>/Gata1<tm8.1Sho>	involves: 129S1/Sv * C57BL/6	N	15895080
MGI:3582858	M	MP:0000600	liver hypoplasia	Gata1<tm7Sho>/Y	involves: 129S1/Sv * C57BL/6	N	15895080
MGI:3582858	M	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm7Sho>/Y	involves: 129S1/Sv * C57BL/6	N	15895080
MGI:3582858	M	MP:0000603	pale liver	Gata1<tm7Sho>/Y	involves: 129S1/Sv * C57BL/6	N	15895080
MGI:3582858	M	MP:0000245	abnormal erythropoiesis	Gata1<tm7Sho>/Y	involves: 129S1/Sv * C57BL/6	N	15895080
MGI:3582859	M	MP:0002417	abnormal megakaryocyte morphology	Gata1<tm8.1Sho>/Y	involves: 129S1/Sv * C57BL/6	N	15895080
MGI:3582871	F	MP:0001926	female infertility	Krt8<tm1Rgo>/Krt8<tm1Rgo>	involves: 129S2/SvPas * C57BL/6 * FVB/N	N	7528156
MGI:3583193	M	MP:0002161	abnormal fertility/fecundity	Irs4<tm1Lhd>/Y	involves: 129S4/SvJae * BALB/c	N	10644546
MGI:3583193	M	MP:0005293	impaired glucose tolerance	Irs4<tm1Lhd>/Y	involves: 129S4/SvJae * BALB/c	N	10644546
MGI:3583193	M	MP:0001935	decreased litter size	Irs4<tm1Lhd>/Y	involves: 129S4/SvJae * BALB/c	N	10644546
MGI:3583221	M	MP:0000664	small prostate gland anterior lobe	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	15831525
MGI:3583221	M	MP:0002675	asthenozoospermia	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	15831525
MGI:3583221	F	MP:0009664	abnormal luminal closure	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	16176985
MGI:3583221	M	MP:0031378	ambiguous external male genitalia	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	15831525
MGI:3583221	F	MP:0009662	abnormal uterine receptivity	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	16176985
MGI:3583221	M	MP:0002789	male pseudohermaphroditism	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	15831525
MGI:3583221	M	MP:0001157	small seminal vesicle	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	15831525
MGI:3583221	M	MP:0001925	male infertility	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	15831525
MGI:3583221	M	MP:0001925	male infertility	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	16176985
MGI:3583221	M	MP:0001158	abnormal prostate gland morphology	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	15831525
MGI:3583221	M	MP:0031286	unilateral cryptorchism	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	15831525
MGI:3583221	M	MP:0002771	absent prostate gland anterior lobe	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	15831525
MGI:3583221	F	MP:0001926	female infertility	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	16176985
MGI:3583221	M	MP:0002059	abnormal seminal vesicle morphology	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	15831525
MGI:3583221	M	MP:0001146	abnormal testis morphology	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	involves: 129X1/SvJ * C57BL/6	N	15831525
MGI:3583265	M	MP:0001732	postnatal growth retardation	Irs1<tm1Jos>/Irs1<tm1Jos>,Irs4<tm1Lhd>/Y	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	N	12502742
MGI:3583265	M	MP:0005293	impaired glucose tolerance	Irs1<tm1Jos>/Irs1<tm1Jos>,Irs4<tm1Lhd>/Y	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	N	12502742
MGI:3583265	M	MP:0005331	insulin resistance	Irs1<tm1Jos>/Irs1<tm1Jos>,Irs4<tm1Lhd>/Y	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	N	12502742
MGI:3583265	M	MP:0002079	increased circulating insulin level	Irs1<tm1Jos>/Irs1<tm1Jos>,Irs4<tm1Lhd>/Y	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	N	12502742
MGI:3583266	F	MP:0001732	postnatal growth retardation	Irs1<tm1Jos>/Irs1<tm1Jos>,Irs4<tm1Lhd>/Irs4<tm1Lhd>	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	N	12502742
MGI:3583266	F	MP:0005331	insulin resistance	Irs1<tm1Jos>/Irs1<tm1Jos>,Irs4<tm1Lhd>/Irs4<tm1Lhd>	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	N	12502742
MGI:3583266	F	MP:0002079	increased circulating insulin level	Irs1<tm1Jos>/Irs1<tm1Jos>,Irs4<tm1Lhd>/Irs4<tm1Lhd>	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	N	12502742
MGI:3583266	F	MP:0005293	impaired glucose tolerance	Irs1<tm1Jos>/Irs1<tm1Jos>,Irs4<tm1Lhd>/Irs4<tm1Lhd>	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	N	12502742
MGI:3583282	F	MP:0013400	abnormal endometrial gland development	Bmpr1b<tm1Kml>/Bmpr1b<tm1Kml>	involves: 129S/SvEv * C57BL/6J	N	11416163
MGI:3583282	F	MP:0001926	female infertility	Bmpr1b<tm1Kml>/Bmpr1b<tm1Kml>	involves: 129S/SvEv * C57BL/6J	N	11416163
MGI:3583282	F	MP:0008258	thin endometrium	Bmpr1b<tm1Kml>/Bmpr1b<tm1Kml>	involves: 129S/SvEv * C57BL/6J	N	11416163
MGI:3583282	F	MP:0009097	absent endometrial glands	Bmpr1b<tm1Kml>/Bmpr1b<tm1Kml>	involves: 129S/SvEv * C57BL/6J	N	11416163
MGI:3583282	F	MP:0009011	prolonged diestrus	Bmpr1b<tm1Kml>/Bmpr1b<tm1Kml>	involves: 129S/SvEv * C57BL/6J	N	11416163
MGI:3583282	F	MP:0009374	absent cumulus expansion	Bmpr1b<tm1Kml>/Bmpr1b<tm1Kml>	involves: 129S/SvEv * C57BL/6J	N	11416163
MGI:3583331	M	MP:0001925	male infertility	Ret<tm2.1Cos>/Ret<tm2.1Cos>	involves: 129S1/Sv * C57BL/6J * FVB/N	N	10675330
MGI:3583763	F	MP:0005185	decreased circulating progesterone level	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0001433	polyphagia	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0001923	reduced female fertility	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0001129	impaired ovarian folliculogenesis	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	M	MP:0001559	hyperglycemia	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	14617753
MGI:3583763	M	MP:0002078	abnormal glucose homeostasis	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11812758
MGI:3583763	F	MP:0002773	decreased circulating luteinizing hormone level	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0031422	failure of superovulation	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0010024	increased total body fat amount	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0001377	abnormal mating frequency	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0009009	absent estrous cycle	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0001127	small ovary	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0005121	decreased circulating prolactin level	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0005431	decreased oocyte number	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0001134	absent corpus luteum	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0001926	female infertility	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0005448	abnormal energy homeostasis	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0005669	increased circulating leptin level	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0011125	decreased primary ovarian follicle number	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	M	MP:0001922	reduced male fertility	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0005181	decreased circulating estradiol level	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	M	MP:0001262	decreased body weight	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11812758
MGI:3583763	F	MP:0001931	abnormal oogenesis	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0008869	anovulation	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0002780	decreased circulating testosterone level	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0001131	abnormal ovarian follicle morphology	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583763	F	MP:0001261	obese	Irs2<tm1Mfw>/Irs2<tm1Mfw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11014193
MGI:3583766	F	MP:0009211	absent external female genitalia	Shh<Dsh>/Shh<Dsh>	involves: 101 * C3H * C57BL * SEC	N	MGI:62282
MGI:3583766	M	MP:0009204	absent external male genitalia	Shh<Dsh>/Shh<Dsh>	involves: 101 * C3H * C57BL * SEC	N	8270769
MGI:3583766	M	MP:0009204	absent external male genitalia	Shh<Dsh>/Shh<Dsh>	involves: 101 * C3H * C57BL * SEC	N	MGI:62282
MGI:3583766	F	MP:0009211	absent external female genitalia	Shh<Dsh>/Shh<Dsh>	involves: 101 * C3H * C57BL * SEC	N	8270769
MGI:3583775	M	MP:0002687	oligozoospermia	Insr<tm1Khn>/Insr<tm1Khn>,Tg(Nes-cre)1Kln/0	involves: 129S4/SvJae * C57BL/6J * SJL	N	11000114
MGI:3583775	F	MP:0011129	decreased tertiary ovarian follicle number	Insr<tm1Khn>/Insr<tm1Khn>,Tg(Nes-cre)1Kln/0	involves: 129S4/SvJae * C57BL/6J * SJL	N	11000114
MGI:3583775	M	MP:0001156	abnormal spermatogenesis	Insr<tm1Khn>/Insr<tm1Khn>,Tg(Nes-cre)1Kln/0	involves: 129S4/SvJae * C57BL/6J * SJL	N	11000114
MGI:3583775	M	MP:0002216	abnormal seminiferous tubule morphology	Insr<tm1Khn>/Insr<tm1Khn>,Tg(Nes-cre)1Kln/0	involves: 129S4/SvJae * C57BL/6J * SJL	N	11000114
MGI:3583775	M	MP:0001922	reduced male fertility	Insr<tm1Khn>/Insr<tm1Khn>,Tg(Nes-cre)1Kln/0	involves: 129S4/SvJae * C57BL/6J * SJL	N	11000114
MGI:3583775	M	MP:0005536	decreased Leydig cell number	Insr<tm1Khn>/Insr<tm1Khn>,Tg(Nes-cre)1Kln/0	involves: 129S4/SvJae * C57BL/6J * SJL	N	11000114
MGI:3583775	F	MP:0002680	decreased corpora lutea number	Insr<tm1Khn>/Insr<tm1Khn>,Tg(Nes-cre)1Kln/0	involves: 129S4/SvJae * C57BL/6J * SJL	N	11000114
MGI:3583781	F	MP:0001126	abnormal ovary morphology	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	N	15935783
MGI:3583781	M	MP:0001925	male infertility	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	N	15935783
MGI:3583781	M	MP:0008261	arrest of male meiosis	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	N	15935783
MGI:3583781	F	MP:0004805	absent oocytes	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	N	15935783
MGI:3583781	F	MP:0002777	absent ovarian follicles	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	N	15935783
MGI:3583781	M	MP:0002216	abnormal seminiferous tubule morphology	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	N	15935783
MGI:3583781	F	MP:0001926	female infertility	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	N	15935783
MGI:3583781	M	MP:0005159	azoospermia	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	N	15935783
MGI:3583781	F	MP:0005168	abnormal female meiosis	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	N	15935783
MGI:3583781	F	MP:0001119	abnormal female reproductive system morphology	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	N	15935783
MGI:3583800	M	MP:0002089	abnormal postnatal growth/weight/body size	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0001262	decreased body weight	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0005459	decreased percent body fat/body weight	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0005334	abnormal fat pad morphology	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0009293	decreased inguinal fat pad weight	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0009289	decreased epididymal fat pad weight	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0005560	decreased circulating glucose level	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0011016	increased core body temperature	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0005449	abnormal food intake	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0009115	abnormal fat cell morphology	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0005292	improved glucose tolerance	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0008965	increased basal metabolism	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0005668	decreased circulating leptin level	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0005379	endocrine/exocrine gland phenotype	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	Y	10891488
MGI:3583800	M	MP:0001783	decreased white adipose tissue amount	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0009295	decreased interscapular fat pad weight	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0002727	decreased circulating insulin level	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583800	M	MP:0000683	decreased percent water in carcass	Ptpn1<tm1Bbk>/Ptpn1<tm1Bbk>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583815	M	MP:0005668	decreased circulating leptin level	Ptpn1<tm1Bbk>/Ptpn1<+>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583815	M	MP:0001262	decreased body weight	Ptpn1<tm1Bbk>/Ptpn1<+>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583815	M	MP:0002089	abnormal postnatal growth/weight/body size	Ptpn1<tm1Bbk>/Ptpn1<+>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583815	M	MP:0002727	decreased circulating insulin level	Ptpn1<tm1Bbk>/Ptpn1<+>	involves: 129S4/SvJae * C57BL/6J	N	10891488
MGI:3583904	M	MP:0011941	increased fluid intake	Ins2<Akita>/Ins2<+>	C57BL/6-Ins2<Akita>	N	17334640
MGI:3583904	M	MP:0002083	premature death	Ins2<Akita>/Ins2<+>	C57BL/6-Ins2<Akita>	N	9133560
MGI:3583904	M	MP:0001363	increased anxiety-related response	Ins2<Akita>/Ins2<+>	C57BL/6-Ins2<Akita>	N	17334640
MGI:3583904	M	MP:0001402	decreased locomotor activity	Ins2<Akita>/Ins2<+>	C57BL/6-Ins2<Akita>	N	17334640
MGI:3583904	M	MP:0002786	abnormal Leydig cell morphology	Ins2<Akita>/Ins2<+>	C57BL/6-Ins2<Akita>	N	16604193
MGI:3583904	M	MP:0001433	polyphagia	Ins2<Akita>/Ins2<+>	C57BL/6-Ins2<Akita>	N	17334640
MGI:3583904	M	MP:0001262	decreased body weight	Ins2<Akita>/Ins2<+>	C57BL/6-Ins2<Akita>	N	17334640
MGI:3583904	M	MP:0002690	akinesia	Ins2<Akita>/Ins2<+>	C57BL/6-Ins2<Akita>	N	17334640
MGI:3583904	M	MP:0001559	hyperglycemia	Ins2<Akita>/Ins2<+>	C57BL/6-Ins2<Akita>	N	17334640
MGI:3583917	M	MP:0001402	decreased locomotor activity	Mecp2<tm1Jchr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	15492925
MGI:3583917	M	MP:0000745	tremors	Mecp2<tm1Jchr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	15492925
MGI:3583917	M	MP:0001409	increased stereotypic behavior	Mecp2<tm1Jchr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	15492925
MGI:3583917	M	MP:0002083	premature death	Mecp2<tm1Jchr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	15492925
MGI:3584104	M	MP:0003205	testicular atrophy	Polg<tm1Prol>/Polg<tm1Prol>	involves: 129S7/SvEvBrd * C57BL/6J * ICR	N	16020738
MGI:3584105	F	MP:0001728	failure of embryo implantation	Zfp830<tm1Cota>/Zfp830<tm1Cota>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6N)	N	15988037
MGI:3584140	F	MP:0001386	abnormal maternal nurturing	Cspg5<tm1Fgr>/Cspg5<tm1Fgr>	B6.129P2-Cspg5<tm1Fgr>	N	15848802
MGI:3584387	F	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis	Irak1<tm1Jth>/Irak1<tm1Jth>	B6.Cg-Irak1<tm1Jth>	N	12626533
MGI:3584433	F	MP:0004047	abnormal milk composition	Wap<tm1Kuw>/Wap<tm1Kuw>	involves: 129X1/SvJ * C57BL/6	N	16106354
MGI:3586344	F	MP:0003579	increased ovarian carcinoma incidence	Csf2<tm1Dran>/Csf2<tm1Dran>,Ifng<tm1Ts>/Ifng<tm1Ts>,Il3<tm1Glli>/Il3<tm1Glli>	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	N	12732663
MGI:3586620	F	MP:0000266	abnormal heart morphology	Irak1<tm1Jth>/Irak1<tm1Jth>,Tg(Myh6-Tnf)1Brgi/?	involves: 129/Sv * C57BL/6J * SJL	N	12860565
MGI:3586620	F	MP:0001856	myocarditis	Irak1<tm1Jth>/Irak1<tm1Jth>,Tg(Myh6-Tnf)1Brgi/?	involves: 129/Sv * C57BL/6J * SJL	N	12860565
MGI:3586620	F	MP:0010768	mortality/aging	Irak1<tm1Jth>/Irak1<tm1Jth>,Tg(Myh6-Tnf)1Brgi/?	involves: 129/Sv * C57BL/6J * SJL	Y	12860565
MGI:3586620	F	MP:0004566	myocardial fiber degeneration	Irak1<tm1Jth>/Irak1<tm1Jth>,Tg(Myh6-Tnf)1Brgi/?	involves: 129/Sv * C57BL/6J * SJL	N	12860565
MGI:3586621	M	MP:0004566	myocardial fiber degeneration	Irak1<tm1Jth>/Y,Tg(Myh6-Tnf)1Brgi/?	involves: 129/Sv * C57BL/6J * SJL	N	12860565
MGI:3586621	M	MP:0001856	myocarditis	Irak1<tm1Jth>/Y,Tg(Myh6-Tnf)1Brgi/?	involves: 129/Sv * C57BL/6J * SJL	N	12860565
MGI:3586621	M	MP:0000266	abnormal heart morphology	Irak1<tm1Jth>/Y,Tg(Myh6-Tnf)1Brgi/?	involves: 129/Sv * C57BL/6J * SJL	N	12860565
MGI:3586621	M	MP:0010768	mortality/aging	Irak1<tm1Jth>/Y,Tg(Myh6-Tnf)1Brgi/?	involves: 129/Sv * C57BL/6J * SJL	Y	12860565
MGI:3586624	M	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis	Irak1<tm1Jth>/Y	B6.Cg-Irak1<tm1Jth>	N	12626533
MGI:3586756	M	MP:0001559	hyperglycemia	Lepr<db-3J>/Lepr<db-3J>	129P3/J-Lepr<db-3J>/J	N	6993269
MGI:3587031	F	MP:0001135	abnormal uterine cervix morphology	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587031	M	MP:0009740	small prostate gland dorsolateral lobe	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10210434
MGI:3587031	M	MP:0013323	abnormal ampullary gland morphology	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10210434
MGI:3587031	M	MP:0000661	small prostate gland ventral lobe	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10210434
MGI:3587031	M	MP:0002059	abnormal seminal vesicle morphology	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10210434
MGI:3587031	M	MP:0000666	decreased prostate gland duct number	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10210434
MGI:3587031	M	MP:0001157	small seminal vesicle	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10210434
MGI:3587031	M	MP:0001163	abnormal prostate gland anterior lobe morphology	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10210434
MGI:3587031	M	MP:0013318	abnormal branching involved in seminal vesicle morphogenesis	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10210434
MGI:3587032	M	MP:0009103	abnormal penile bone morphology	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	F	MP:0001926	female infertility	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	M	MP:0003617	urinary bladder hypoplasia	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	F	MP:0008983	small vagina	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	F	MP:0003446	renal hypoplasia	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	F	MP:0011780	abnormal female urethra morphology	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	M	MP:0003270	intestinal obstruction	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	F	MP:0003550	short perineum	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	F	MP:0001135	abnormal uterine cervix morphology	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	F	MP:0000516	abnormal renal/urinary system morphology	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	M	MP:0001925	male infertility	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	M	MP:0011828	urinary bladder cyst	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	F	MP:0011829	vesicovaginal fistula	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	F	MP:0003675	kidney cyst	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	F	MP:0009227	uterine cervix hypoplasia	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	F	MP:0009087	dilated uterine horn	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	F	MP:0009252	absent urinary bladder	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587032	M	MP:0009104	small penile bone	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	N	10569982
MGI:3587188	M	MP:0002059	abnormal seminal vesicle morphology	Hoxd13<spdh>/Hoxd13<spdh>	B6C3Fe a/a-Hoxd13<spdh>/J	N	9580668
MGI:3587188	M	MP:0001925	male infertility	Hoxd13<spdh>/Hoxd13<spdh>	B6C3Fe a/a-Hoxd13<spdh>/J	N	9580668
MGI:3587188	M	MP:0006401	absent male preputial gland	Hoxd13<spdh>/Hoxd13<spdh>	B6C3Fe a/a-Hoxd13<spdh>/J	N	9580668
MGI:3587647	M	MP:0001925	male infertility	Tg(Cyp19)C2-3Rrte/0	involves: BALB/c * C57BL/6	N	10623684
MGI:3587647	F	MP:0001885	mammary gland duct hyperplasia	Tg(Cyp19)C2-3Rrte/0	involves: BALB/c * C57BL/6	N	8764102
MGI:3587647	F	MP:0000630	mammary gland hyperplasia	Tg(Cyp19)C2-3Rrte/0	involves: BALB/c * C57BL/6	N	11358670
MGI:3587647	F	MP:0000630	mammary gland hyperplasia	Tg(Cyp19)C2-3Rrte/0	involves: BALB/c * C57BL/6	N	8764102
MGI:3587647	M	MP:0001148	enlarged testis	Tg(Cyp19)C2-3Rrte/0	involves: BALB/c * C57BL/6	N	10623684
MGI:3587737	M	MP:0002840	abnormal lens fiber morphology	Nhs<Xcat>/Y	involves: DBA/2 * T STOCK	N	8282045
MGI:3587737	M	MP:0003236	abnormal lens capsule morphology	Nhs<Xcat>/Y	involves: DBA/2 * T STOCK	N	8282045
MGI:3587737	M	MP:0001304	cataract	Nhs<Xcat>/Y	involves: DBA/2 * T STOCK	N	2272505
MGI:3587737	M	MP:0008841	ruptured lens capsule	Nhs<Xcat>/Y	involves: DBA/2 * T STOCK	N	8282045
MGI:3587737	M	MP:0011697	lens vacuoles	Nhs<Xcat>/Y	involves: DBA/2 * T STOCK	N	8282045
MGI:3587737	M	MP:0010263	total cataract	Nhs<Xcat>/Y	involves: DBA/2 * T STOCK	N	MGI:62294
MGI:3587737	M	MP:0001304	cataract	Nhs<Xcat>/Y	involves: DBA/2 * T STOCK	N	8282045
MGI:3587737	M	MP:0001303	abnormal lens morphology	Nhs<Xcat>/Y	involves: DBA/2 * T STOCK	N	8282045
MGI:3587738	F	MP:0001303	abnormal lens morphology	Nhs<Xcat>/Nhs<Xcat>	involves: DBA/2 * T STOCK	N	8282045
MGI:3587738	F	MP:0003236	abnormal lens capsule morphology	Nhs<Xcat>/Nhs<Xcat>	involves: DBA/2 * T STOCK	N	8282045
MGI:3587738	F	MP:0002840	abnormal lens fiber morphology	Nhs<Xcat>/Nhs<Xcat>	involves: DBA/2 * T STOCK	N	8282045
MGI:3587738	F	MP:0008841	ruptured lens capsule	Nhs<Xcat>/Nhs<Xcat>	involves: DBA/2 * T STOCK	N	8282045
MGI:3587738	F	MP:0010263	total cataract	Nhs<Xcat>/Nhs<Xcat>	involves: DBA/2 * T STOCK	N	MGI:62294
MGI:3587738	F	MP:0001304	cataract	Nhs<Xcat>/Nhs<Xcat>	involves: DBA/2 * T STOCK	N	8282045
MGI:3587738	F	MP:0001304	cataract	Nhs<Xcat>/Nhs<Xcat>	involves: DBA/2 * T STOCK	N	2272505
MGI:3587738	F	MP:0011697	lens vacuoles	Nhs<Xcat>/Nhs<Xcat>	involves: DBA/2 * T STOCK	N	8282045
MGI:3587739	F	MP:0001304	cataract	Nhs<Xcat>/Nhs<+>	involves: DBA/2 * T STOCK	N	2272505
MGI:3587739	F	MP:0001304	cataract	Nhs<Xcat>/Nhs<+>	involves: DBA/2 * T STOCK	N	8282045
MGI:3587739	F	MP:0001304	cataract	Nhs<Xcat>/Nhs<+>	involves: DBA/2 * T STOCK	N	MGI:62294
MGI:3587801	F	MP:0003809	abnormal hair shaft morphology	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	6682087
MGI:3587801	F	MP:0002110	abnormal digit morphology	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	6682087
MGI:3587801	F	MP:0002109	abnormal limb morphology	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	6682087
MGI:3587801	F	MP:0002111	abnormal tail morphology	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	6682087
MGI:3587801	F	MP:0000367	abnormal coat/ hair morphology	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	6682087
MGI:3587801	F	MP:0000414	alopecia	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	6682087
MGI:3587801	F	MP:0000414	alopecia	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	4588955
MGI:3587801	F	MP:0003417	premature endochondral bone ossification	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	6682087
MGI:3587801	F	MP:0011086	postnatal lethality, incomplete penetrance	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	15639195
MGI:3587801	F	MP:0000372	irregular coat pigmentation	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	4588955
MGI:3587801	F	MP:0001304	cataract	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	6682087
MGI:3587801	F	MP:0002544	brachydactyly	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	4588955
MGI:3587801	F	MP:0002772	brachypodia	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	4588955
MGI:3587801	F	MP:0000547	short limbs	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	6682087
MGI:3587801	F	MP:0001242	hyperkeratosis	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	6682087
MGI:3587801	F	MP:0000585	kinked tail	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	6682087
MGI:3587801	F	MP:0001511	disheveled coat	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	4588955
MGI:3587801	F	MP:0001511	disheveled coat	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	6682087
MGI:3587801	F	MP:0001265	decreased body size	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	4588955
MGI:3587801	F	MP:0011090	perinatal lethality, incomplete penetrance	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	15639195
MGI:3587801	F	MP:0000592	short tail	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	6682087
MGI:3587801	F	MP:0006253	clinodactyly	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	4588955
MGI:3587801	F	MP:0001262	decreased body weight	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	4588955
MGI:3587801	F	MP:0001386	abnormal maternal nurturing	Nsdhl<Bpa-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	4588955
MGI:3587802	M	MP:0011523	thin placenta labyrinth	Nsdhl<Bpa-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3587802	M	MP:0004259	small placenta	Nsdhl<Bpa-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3587802	M	MP:0011527	disorganized placental labyrinth	Nsdhl<Bpa-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3587802	M	MP:0003717	pallor	Nsdhl<Bpa-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3587802	M	MP:0004076	abnormal vitelline vascular remodeling	Nsdhl<Bpa-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3587802	M	MP:0011091	prenatal lethality, complete penetrance	Nsdhl<Bpa-1H>/Y	involves: 101/H * C3H/HeH	N	4588955
MGI:3587802	M	MP:0001722	pale yolk sac	Nsdhl<Bpa-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3587802	M	MP:0011091	prenatal lethality, complete penetrance	Nsdhl<Bpa-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3587802	M	MP:0001698	decreased embryo size	Nsdhl<Bpa-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3587802	M	MP:0003984	embryonic growth retardation	Nsdhl<Bpa-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3587819	M	MP:0011091	prenatal lethality, complete penetrance	Ebp<Td>/Y	Not Specified	N	MGI:62085
MGI:3587820	F	MP:0001262	decreased body weight	Ebp<Td>/Ebp<+>	Not Specified	N	MGI:62085
MGI:3587820	F	MP:0000414	alopecia	Ebp<Td>/Ebp<+>	Not Specified	N	MGI:62085
MGI:3587820	F	MP:0001212	skin lesions	Ebp<Td>/Ebp<+>	Not Specified	N	MGI:62085
MGI:3587820	F	MP:0001265	decreased body size	Ebp<Td>/Ebp<+>	Not Specified	N	MGI:62085
MGI:3587820	F	MP:0001195	flaky skin	Ebp<Td>/Ebp<+>	Not Specified	N	MGI:62085
MGI:3587820	F	MP:0011101	prenatal lethality, incomplete penetrance	Ebp<Td>/Ebp<+>	Not Specified	N	MGI:62085
MGI:3587820	F	MP:0011086	postnatal lethality, incomplete penetrance	Ebp<Td>/Ebp<+>	Not Specified	N	MGI:62085
MGI:3587823	M	MP:0011523	thin placenta labyrinth	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587823	M	MP:0001914	hemorrhage	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587823	M	MP:0003984	embryonic growth retardation	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587823	M	MP:0011091	prenatal lethality, complete penetrance	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	14567972
MGI:3587823	M	MP:0001698	decreased embryo size	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587823	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587823	M	MP:0001716	abnormal placenta labyrinth morphology	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587823	M	MP:0005312	pericardial effusion	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587823	M	MP:0001722	pale yolk sac	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587823	M	MP:0004259	small placenta	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587823	M	MP:0011091	prenatal lethality, complete penetrance	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	MGI:3044155
MGI:3587823	M	MP:0011527	disorganized placental labyrinth	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587823	M	MP:0004076	abnormal vitelline vascular remodeling	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587823	M	MP:0000783	abnormal forebrain morphology	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587823	M	MP:0003717	pallor	Nsdhl<Bpa-8H>/Y	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587824	F	MP:0000372	irregular coat pigmentation	Nsdhl<Bpa-8H>/Nsdhl<+>	involves: BALB/c * C3H/HeN	N	MGI:3044155
MGI:3587824	F	MP:0000414	alopecia	Nsdhl<Bpa-8H>/Nsdhl<+>	involves: BALB/c * C3H/HeN	N	14567972
MGI:3587824	F	MP:0001191	abnormal skin condition	Nsdhl<Bpa-8H>/Nsdhl<+>	involves: BALB/c * C3H/HeN	N	MGI:3044155
MGI:3587824	F	MP:0001191	abnormal skin condition	Nsdhl<Bpa-8H>/Nsdhl<+>	involves: BALB/c * C3H/HeN	N	14567972
MGI:3587824	F	MP:0001265	decreased body size	Nsdhl<Bpa-8H>/Nsdhl<+>	involves: BALB/c * C3H/HeN	N	MGI:3044155
MGI:3587824	F	MP:0001265	decreased body size	Nsdhl<Bpa-8H>/Nsdhl<+>	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587824	F	MP:0001242	hyperkeratosis	Nsdhl<Bpa-8H>/Nsdhl<+>	involves: BALB/c * C3H/HeN	N	14567972
MGI:3587824	F	MP:0001242	hyperkeratosis	Nsdhl<Bpa-8H>/Nsdhl<+>	involves: BALB/c * C3H/HeN	N	15639195
MGI:3587825	M	MP:0002080	prenatal lethality	Nsdhl<Bpa-7H>/Y	Not Specified	N	14567972
MGI:3587826	F	MP:0001191	abnormal skin condition	Nsdhl<Bpa-7H>/Nsdhl<+>	Not Specified	N	14567972
MGI:3587826	F	MP:0000414	alopecia	Nsdhl<Bpa-7H>/Nsdhl<+>	Not Specified	N	14567972
MGI:3587826	F	MP:0001242	hyperkeratosis	Nsdhl<Bpa-7H>/Nsdhl<+>	Not Specified	N	14567972
MGI:3587904	M	MP:0031286	unilateral cryptorchism	Bmp5<se>/Bmp5<se>	SEAC/Gn	N	5692092
MGI:3587904	F	MP:0011727	ectopic ovary	Bmp5<se>/Bmp5<se>	SEAC/Gn	N	5692092
MGI:3587920	F	MP:0011727	ectopic ovary	Bmp5<se-Ca>/Bmp5<se-Ca>	SEACGn.CB-Bmp5<se-Ca>	N	5692092
MGI:3587920	M	MP:0031286	unilateral cryptorchism	Bmp5<se-Ca>/Bmp5<se-Ca>	SEACGn.CB-Bmp5<se-Ca>	N	5692092
MGI:3587945	M	MP:0005075	abnormal melanosome morphology	Gpr143<tm1Inc>/Y	either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)	N	11092754
MGI:3587945	M	MP:0005199	abnormal iris pigment epithelium	Gpr143<tm1Inc>/Y	either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)	N	11092754
MGI:3587945	M	MP:0002864	abnormal ocular fundus morphology	Gpr143<tm1Inc>/Y	either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)	N	11092754
MGI:3587945	M	MP:0005101	abnormal ciliary body pigmentation	Gpr143<tm1Inc>/Y	either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)	N	11092754
MGI:3587945	M	MP:0005103	abnormal retina pigmentation	Gpr143<tm1Inc>/Y	either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)	N	11092754
MGI:3587945	M	MP:0005201	abnormal retina pigment epithelium morphology	Gpr143<tm1Inc>/Y	either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)	N	11092754
MGI:3587945	M	MP:0001332	abnormal optic nerve innervation	Gpr143<tm1Inc>/Y	either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)	N	11092754
MGI:3588036	M	MP:0002730	head shaking	Pou3f4<Slf>/Y	C3H101H-Pou3f4<Slf>	N	MGI:61922
MGI:3588036	M	MP:0003069	abnormal superior semicircular canal morphology	Pou3f4<Slf>/Y	C3H101H-Pou3f4<Slf>	N	10587581
MGI:3588036	M	MP:0004292	abnormal spiral ligament fibrocyte morphology	Pou3f4<Slf>/Y	C3H101H-Pou3f4<Slf>	N	10587581
MGI:3588037	F	MP:0003069	abnormal superior semicircular canal morphology	Pou3f4<Slf>/Pou3f4<Slf>	C3H101H-Pou3f4<Slf>	N	10587581
MGI:3588037	F	MP:0004292	abnormal spiral ligament fibrocyte morphology	Pou3f4<Slf>/Pou3f4<Slf>	C3H101H-Pou3f4<Slf>	N	10587581
MGI:3588037	F	MP:0001485	abnormal pinna reflex	Pou3f4<Slf>/Pou3f4<Slf>	C3H101H-Pou3f4<Slf>	N	10587581
MGI:3588037	F	MP:0002730	head shaking	Pou3f4<Slf>/Pou3f4<Slf>	C3H101H-Pou3f4<Slf>	N	MGI:61922
MGI:3588102	F	MP:0001934	increased litter size	Anxa7<tm1Pll>/Anxa7<+>	B6.Cg-Anxa7<tm1Pll>	N	32923441
MGI:3588102	F	MP:0005389	reproductive system phenotype	Anxa7<tm1Pll>/Anxa7<+>	B6.Cg-Anxa7<tm1Pll>	Y	32923441
MGI:3588102	F	MP:0001727	abnormal embryo implantation	Anxa7<tm1Pll>/Anxa7<+>	B6.Cg-Anxa7<tm1Pll>	N	32923441
MGI:3588102	F	MP:0009662	abnormal uterine receptivity	Anxa7<tm1Pll>/Anxa7<+>	B6.Cg-Anxa7<tm1Pll>	N	32923441
MGI:3588501	F	MP:0020491	abnormal ovary topology	Gdnf<tm1Rosl>/Gdnf<tm1Rosl>	involves: 129S2/SvPas	N	8657308
MGI:3588568	M	MP:0004852	decreased testis weight	Tg(Gnrh1-Fgfr1)1Tsai/Tg(Gnrh1-Fgfr1)1Tsai	involves: C57BL/6J * DBA/2J	N	15459253
MGI:3588579	M	MP:0001925	male infertility	Hjv<tm1Arbr>/Hjv<tm1Arbr>	involves: 129S4/SvJae * 129X1/SvJ	N	16075058
MGI:3588712	F	MP:0002411	decreased susceptibility to bacterial infection	Ses1a<C57BL/6J>/Ses1a<C57BL/6J>,Ses4<C57BL/6J>/Ses4<C57BL/6J>	involves: 129S6/SvEvTac * C57BL/6J	N	15973461
MGI:3589255	F	MP:0001473	reduced long-term potentiation	Pak3<tm1Zpj>/Pak3<tm1Zpj>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	16014725
MGI:3589255	F	MP:0002805	abnormal conditioned taste aversion behavior	Pak3<tm1Zpj>/Pak3<tm1Zpj>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	16014725
MGI:3589400	F	MP:0011967	increased or absent threshold for auditory brainstem response	tmgc47/tmgc47	mixed	N	MGI:3053008
MGI:3589400	F	MP:0005189	abnormal anogenital distance	tmgc47/tmgc47	mixed	N	MGI:3053008
MGI:3589400	F	MP:0006325	impaired hearing	tmgc47/tmgc47	mixed	N	MGI:3053008
MGI:3589409	M	MP:0002871	albuminuria	Alms1<Gt(XH152)Byg>/Alms1<Gt(XH152)Byg>	involves: 129P2/OlaHsd * C57BL/6J	N	16000322
MGI:3589409	M	MP:0002216	abnormal seminiferous tubule morphology	Alms1<Gt(XH152)Byg>/Alms1<Gt(XH152)Byg>	involves: 129P2/OlaHsd * C57BL/6J	N	16000322
MGI:3589435	F	MP:0001120	abnormal uterus morphology	Chd7<Whi>/Chd7<+>	C3HeB/FeJ-Chd7<Whi>	N	19809474
MGI:3589435	F	MP:0009229	abnormal neurohypophysis median eminence morphology	Chd7<Whi>/Chd7<+>	C3HeB/FeJ-Chd7<Whi>	N	19809474
MGI:3589435	F	MP:0009085	abnormal uterine horn morphology	Chd7<Whi>/Chd7<+>	C3HeB/FeJ-Chd7<Whi>	N	19809474
MGI:3589435	M	MP:0004852	decreased testis weight	Chd7<Whi>/Chd7<+>	C3HeB/FeJ-Chd7<Whi>	N	19809474
MGI:3589435	F	MP:0008948	decreased neuron number	Chd7<Whi>/Chd7<+>	C3HeB/FeJ-Chd7<Whi>	N	19809474
MGI:3589435	M	MP:0001940	testis hypoplasia	Chd7<Whi>/Chd7<+>	C3HeB/FeJ-Chd7<Whi>	N	19809474
MGI:3589453	F	MP:0001510	abnormal coat appearance	Gs/Gs<+>	Not Specified	N	2055107
MGI:3589453	F	MP:0000564	syndactyly	Gs/Gs<+>	Not Specified	N	2055107
MGI:3589453	F	MP:0000562	polydactyly	Gs/Gs<+>	Not Specified	N	2055107
MGI:3589456	F	MP:0001510	abnormal coat appearance	Gs/Gs	Not Specified	N	MGI:63196
MGI:3589456	F	MP:0000411	shiny fur	Gs/Gs	Not Specified	N	MGI:63196
MGI:3589460	M	MP:0005409	darkened coat color	Gs/Y	Not Specified	N	MGI:77872
MGI:3589460	M	MP:0010179	rough coat	Gs/Y	Not Specified	N	MGI:77872
MGI:3589460	M	MP:0001510	abnormal coat appearance	Gs/Y	Not Specified	N	MGI:77872
MGI:3589460	M	MP:0002074	abnormal hair texture	Gs/Y	Not Specified	N	MGI:77872
MGI:3589460	M	MP:0000402	abnormal zigzag hair morphology	Gs/Y	Not Specified	N	MGI:77872
MGI:3589460	M	MP:0003849	greasy coat	Gs/Y	Not Specified	N	MGI:63196
MGI:3589732	M	MP:0001606	impaired hematopoiesis	Gata1<tm9Sho>/Y	Not Specified	N	16107690
MGI:3589775	M	MP:0002687	oligozoospermia	Creb3l4<tm1Imad>/Creb3l4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	16107712
MGI:3589775	M	MP:0020550	multinucleated giant male germ cells	Creb3l4<tm1Imad>/Creb3l4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	16107712
MGI:3589775	M	MP:0002216	abnormal seminiferous tubule morphology	Creb3l4<tm1Imad>/Creb3l4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	16107712
MGI:3589808	F	MP:0009326	absent maternal crouching	Peg3<tm1Masu>/Peg3<+>	involves: 129S1/Sv * 129X1/SvJ	N	10195900
MGI:3589808	F	MP:0001384	abnormal pup retrieval	Peg3<tm1Masu>/Peg3<+>	involves: 129S1/Sv * 129X1/SvJ	N	10195900
MGI:3589818	M	MP:0002687	oligozoospermia	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	18032421
MGI:3589818	M	MP:0006378	abnormal spermatogonia morphology	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	18032421
MGI:3589818	M	MP:0001147	small testis	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	16107850
MGI:3589818	M	MP:0005159	azoospermia	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	16107850
MGI:3589818	M	MP:0002685	abnormal spermatogonia proliferation	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	16107850
MGI:3589818	M	MP:0001156	abnormal spermatogenesis	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	16107850
MGI:3589818	M	MP:0004852	decreased testis weight	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	18032421
MGI:3589818	M	MP:0006379	abnormal spermatocyte morphology	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	16107850
MGI:3589818	M	MP:0002566	abnormal sexual interaction	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	18032421
MGI:3589818	M	MP:0002675	asthenozoospermia	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	18032421
MGI:3589818	M	MP:0001925	male infertility	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	16107850
MGI:3589818	M	MP:0006378	abnormal spermatogonia morphology	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	16107850
MGI:3589818	M	MP:0004182	abnormal spermiation	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	18032421
MGI:3589818	M	MP:0001925	male infertility	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	18032421
MGI:3589818	M	MP:0014052	increased male germ cell apoptosis	Etv5<tm1Kmm>/Etv5<tm1Kmm>	involves: 129S6/SvEvTac	N	18032421
MGI:3589827	F	MP:0001923	reduced female fertility	Ptger2<tm2Bhk>/Ptger2<tm2Bhk>	involves: 129P2/OlaHsd * 129S/SvEv	N	10359563
MGI:3589874	F	MP:0009072	absent cranial vagina	Wnt9b<tm1.1Amc>/Wnt9b<tm1.1Amc>	involves: 129X1/SvJ * C57BL/6 * CBA	N	16054034
MGI:3589874	F	MP:0003576	oviduct hypoplasia	Wnt9b<tm1.1Amc>/Wnt9b<tm1.1Amc>	involves: 129X1/SvJ * C57BL/6 * CBA	N	16054034
MGI:3589874	M	MP:0004727	absent epididymis	Wnt9b<tm1.1Amc>/Wnt9b<tm1.1Amc>	involves: 129X1/SvJ * C57BL/6 * CBA	N	16054034
MGI:3589874	F	MP:0003558	absent uterus	Wnt9b<tm1.1Amc>/Wnt9b<tm1.1Amc>	involves: 129X1/SvJ * C57BL/6 * CBA	N	16054034
MGI:3589874	M	MP:0003557	absent vas deferens	Wnt9b<tm1.1Amc>/Wnt9b<tm1.1Amc>	involves: 129X1/SvJ * C57BL/6 * CBA	N	16054034
MGI:3589923	M	MP:0001192	scaly skin	Foxp3<sf>/Y	involves: STOCK MR	N	MGI:62253
MGI:3589923	M	MP:0001116	small gonad	Foxp3<sf>/Y	involves: STOCK MR	N	MGI:62253
MGI:3589923	M	MP:0001925	male infertility	Foxp3<sf>/Y	involves: STOCK MR	N	16590412
MGI:3589923	M	MP:0001290	delayed eyelid opening	Foxp3<sf>/Y	involves: STOCK MR	N	16590412
MGI:3589923	M	MP:0001192	scaly skin	Foxp3<sf>/Y	involves: STOCK MR	N	16590412
MGI:3589923	M	MP:0002082	postnatal lethality	Foxp3<sf>/Y	involves: STOCK MR	N	16590412
MGI:3589923	M	MP:0002771	absent prostate gland anterior lobe	Foxp3<sf>/Y	involves: STOCK MR	N	MGI:62253
MGI:3589923	M	MP:0001925	male infertility	Foxp3<sf>/Y	involves: STOCK MR	N	MGI:62253
MGI:3589923	M	MP:0001145	abnormal male reproductive system morphology	Foxp3<sf>/Y	involves: STOCK MR	N	16590412
MGI:3589923	M	MP:0002286	cryptorchism	Foxp3<sf>/Y	involves: STOCK MR	N	MGI:62253
MGI:3589923	M	MP:0001198	tight skin	Foxp3<sf>/Y	involves: STOCK MR	N	16590412
MGI:3589923	M	MP:0001147	small testis	Foxp3<sf>/Y	involves: STOCK MR	N	MGI:62253
MGI:3589923	M	MP:0001265	decreased body size	Foxp3<sf>/Y	involves: STOCK MR	N	16590412
MGI:3589923	M	MP:0002670	absent scrotum	Foxp3<sf>/Y	involves: STOCK MR	N	MGI:62253
MGI:3589923	M	MP:0003642	absent seminal vesicle	Foxp3<sf>/Y	involves: STOCK MR	N	MGI:62253
MGI:3589923	M	MP:0002083	premature death	Foxp3<sf>/Y	involves: STOCK MR	N	16590412
MGI:3589925	M	MP:0000602	dilated liver sinusoidal space	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002447	abnormal erythrocyte morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002619	abnormal lymphocyte morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002459	abnormal B cell physiology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001860	liver inflammation	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001147	small testis	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000274	enlarged heart	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002357	abnormal spleen white pulp morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0012246	abnormal hepatic cord morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0004969	pale kidney	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0010334	pleural effusion	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001270	distended abdomen	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0005097	polychromatophilia	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000240	extramedullary hematopoiesis	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001855	abnormal atrial thrombosis	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0005251	blepharitis	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002344	abnormal lymph node B cell domain morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0005150	cachexia	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002347	abnormal lymph node T cell domain morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002874	decreased hemoglobin content	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001265	decreased body size	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002590	increased mean corpuscular volume	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0003427	parakeratosis	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000208	decreased hematocrit	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000703	abnormal thymus morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002642	anisocytosis	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001655	multifocal hepatic necrosis	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001577	anemia	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000599	enlarged liver	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001505	hunched posture	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0008476	increased spleen red pulp amount	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002083	premature death	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001846	increased inflammatory response	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001212	skin lesions	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001145	abnormal male reproductive system morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002339	abnormal lymph node morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001216	abnormal epidermal layer morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002493	increased IgG level	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000611	jaundice	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001222	epidermal hyperplasia	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000706	small thymus	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001192	scaly skin	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000689	abnormal spleen morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002643	poikilocytosis	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0011224	abnormal lymph node medullary cord morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0001194	dermatitis	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0008234	absent spleen marginal zone	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002286	cryptorchism	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002494	increased IgM level	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0014263	decreased spleen B cell follicle number	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000702	enlarged lymph nodes	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000020	scaly ears	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000018	small ears	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0009675	orthokeratosis	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000598	abnormal liver morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0004952	increased spleen weight	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002371	abnormal thymus cortex morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000019	thick ears	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0000218	increased leukocyte cell number	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0012078	abnormal tail ring morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589925	M	MP:0002446	abnormal macrophage morphology	Foxp3<sf>/Y	either: 129Rl.Cg-Foxp3<sf> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	N	2053595
MGI:3589971	M	MP:0002286	cryptorchism	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0003550	short perineum	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0001262	decreased body weight	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0002874	decreased hemoglobin content	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0002447	abnormal erythrocyte morphology	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0002670	absent scrotum	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0000208	decreased hematocrit	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0001951	abnormal breathing pattern	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0000240	extramedullary hematopoiesis	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0001198	tight skin	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0004969	pale kidney	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0001265	decreased body size	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0003179	thrombocytopenia	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0011083	lethality at weaning, complete penetrance	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0001192	scaly skin	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0000689	abnormal spleen morphology	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0000465	gastrointestinal hemorrhage	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0000018	small ears	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0000218	increased leukocyte cell number	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0001116	small gonad	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0005202	lethargy	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0003292	melena	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0000598	abnormal liver morphology	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0008478	increased spleen white pulp amount	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0004952	increased spleen weight	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0008476	increased spleen red pulp amount	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0008475	intermingled spleen red and white pulp	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0005287	narrow eye opening	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0001732	postnatal growth retardation	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0005036	diarrhea	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0002875	decreased erythrocyte cell number	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0002424	abnormal reticulocyte morphology	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0000599	enlarged liver	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0001145	abnormal male reproductive system morphology	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0000603	pale liver	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0001852	conjunctivitis	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0008255	decreased megakaryocyte cell number	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589971	M	MP:0001577	anemia	Foxp3<sf>/Y	involves: 101/H * C3H/HeH * STOCK MR	N	2320565
MGI:3589983	M	MP:0001147	small testis	Aff4<tm1Nosa>/Aff4<tm1Nosa>	involves: 129P2/OlaHsd * C57BL/6	N	16024815
MGI:3589983	M	MP:0004909	increased seminal vesicle weight	Aff4<tm1Nosa>/Aff4<tm1Nosa>	involves: 129P2/OlaHsd * C57BL/6	N	16024815
MGI:3589983	M	MP:0005159	azoospermia	Aff4<tm1Nosa>/Aff4<tm1Nosa>	involves: 129P2/OlaHsd * C57BL/6	N	16024815
MGI:3589983	M	MP:0001155	arrest of spermatogenesis	Aff4<tm1Nosa>/Aff4<tm1Nosa>	involves: 129P2/OlaHsd * C57BL/6	N	16024815
MGI:3589983	M	MP:0004930	small epididymis	Aff4<tm1Nosa>/Aff4<tm1Nosa>	involves: 129P2/OlaHsd * C57BL/6	N	16024815
MGI:3589983	M	MP:0001925	male infertility	Aff4<tm1Nosa>/Aff4<tm1Nosa>	involves: 129P2/OlaHsd * C57BL/6	N	16024815
MGI:3590072	M	MP:0000702	enlarged lymph nodes	Foxp3<sf> Otc<spf>/Y	involves: 129/Rl	N	7930593
MGI:3590072	M	MP:0000691	enlarged spleen	Foxp3<sf> Otc<spf>/Y	involves: 129/Rl	N	7930593
MGI:3590072	M	MP:0008074	increased CD4-positive, alpha-beta T cell number	Foxp3<sf> Otc<spf>/Y	involves: 129/Rl	N	7930593
MGI:3590072	M	MP:0002083	premature death	Foxp3<sf> Otc<spf>/Y	involves: 129/Rl	N	7930593
MGI:3590072	M	MP:0000208	decreased hematocrit	Foxp3<sf> Otc<spf>/Y	involves: 129/Rl	N	7930593
MGI:3590072	M	MP:0011086	postnatal lethality, incomplete penetrance	Foxp3<sf> Otc<spf>/Y	involves: 129/Rl	N	7930593
MGI:3590072	M	MP:0001577	anemia	Foxp3<sf> Otc<spf>/Y	involves: 129/Rl	N	7930593
MGI:3590072	M	MP:0001262	decreased body weight	Foxp3<sf> Otc<spf>/Y	involves: 129/Rl	N	7930593
MGI:3590072	M	MP:0001212	skin lesions	Foxp3<sf> Otc<spf>/Y	involves: 129/Rl	N	7930593
MGI:3590073	M	MP:0008074	increased CD4-positive, alpha-beta T cell number	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0000702	enlarged lymph nodes	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0002493	increased IgG level	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0001265	decreased body size	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0008751	abnormal interleukin level	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0002461	increased immunoglobulin level	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0001577	anemia	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0008097	increased plasma cell number	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0000208	decreased hematocrit	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0008752	abnormal tumor necrosis factor level	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0002722	abnormal immune system organ morphology	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0001194	dermatitis	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0002494	increased IgM level	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0000691	enlarged spleen	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590073	M	MP:0002339	abnormal lymph node morphology	B2m<tm1Jae>/B2m<tm1Jae>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590074	M	MP:0003717	pallor	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3590074	M	MP:0001914	hemorrhage	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3590074	M	MP:0003984	embryonic growth retardation	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3590074	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3590074	M	MP:0004259	small placenta	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3590074	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	MGI:48828
MGI:3590074	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	10369263
MGI:3590074	M	MP:0011527	disorganized placental labyrinth	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3590074	M	MP:0004076	abnormal vitelline vascular remodeling	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3590074	M	MP:0001722	pale yolk sac	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3590074	M	MP:0001716	abnormal placenta labyrinth morphology	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3590074	M	MP:0005312	pericardial effusion	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3590074	M	MP:0001698	decreased embryo size	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3590074	M	MP:0011523	thin placenta labyrinth	Nsdhl<Str-1H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3590076	F	MP:0000160	kyphosis	Nsdhl<Str-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	11005611
MGI:3590076	F	MP:0001325	abnormal retina morphology	Nsdhl<Str-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	11005611
MGI:3590076	F	MP:0000372	irregular coat pigmentation	Nsdhl<Str-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590076	F	MP:0000405	abnormal auchene hair morphology	Nsdhl<Str-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590076	F	MP:0000397	abnormal guard hair morphology	Nsdhl<Str-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590076	F	MP:0001326	retina degeneration	Nsdhl<Str-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	11005611
MGI:3590076	F	MP:0000674	abnormal sweat gland morphology	Nsdhl<Str-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	11005611
MGI:3590076	F	MP:0000372	irregular coat pigmentation	Nsdhl<Str-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	MGI:48828
MGI:3590076	F	MP:0010768	mortality/aging	Nsdhl<Str-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	Y	10369263
MGI:3590076	F	MP:0000417	short hair	Nsdhl<Str-1H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590077	M	MP:0002494	increased IgM level	Cd4<tm1Litt>/Cd4<tm1Litt>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590077	M	MP:0000702	enlarged lymph nodes	Cd4<tm1Litt>/Cd4<tm1Litt>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590077	M	MP:0008699	increased interleukin-4 secretion	Cd4<tm1Litt>/Cd4<tm1Litt>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590077	M	MP:0002083	premature death	Cd4<tm1Litt>/Cd4<tm1Litt>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590077	M	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology	Cd4<tm1Litt>/Cd4<tm1Litt>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590077	M	MP:0008705	increased interleukin-6 secretion	Cd4<tm1Litt>/Cd4<tm1Litt>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590077	M	MP:0003009	abnormal cytokine secretion	Cd4<tm1Litt>/Cd4<tm1Litt>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590077	M	MP:0008560	increased tumor necrosis factor secretion	Cd4<tm1Litt>/Cd4<tm1Litt>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590077	M	MP:0002722	abnormal immune system organ morphology	Cd4<tm1Litt>/Cd4<tm1Litt>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590077	M	MP:0002493	increased IgG level	Cd4<tm1Litt>/Cd4<tm1Litt>,Foxp3<sf> Otc<spf>/Y	involves: 129/Rl * 129S2/SvPas	N	7930593
MGI:3590078	F	MP:0002940	variable body spotting	Nsdhl<Str-1Or>/Nsdhl<+>	involves: 101/Rl * C3H/Rl	N	10369263
MGI:3590078	F	MP:0000367	abnormal coat/ hair morphology	Nsdhl<Str-1Or>/Nsdhl<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3590078	F	MP:0000372	irregular coat pigmentation	Nsdhl<Str-1Or>/Nsdhl<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3590078	F	MP:0000372	irregular coat pigmentation	Nsdhl<Str-1Or>/Nsdhl<+>	involves: 101/Rl * C3H/Rl	N	10369263
MGI:3590079	M	MP:0011091	prenatal lethality, complete penetrance	Nsdhl<Str-1Or>/Y	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3590079	M	MP:0004259	small placenta	Nsdhl<Str-1Or>/Y	involves: 101/Rl * C3H/Rl	N	15639195
MGI:3590079	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Nsdhl<Str-1Or>/Y	involves: 101/Rl * C3H/Rl	N	10369263
MGI:3590079	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Nsdhl<Str-1Or>/Y	involves: 101/Rl * C3H/Rl	N	15639195
MGI:3590080	F	MP:0011091	prenatal lethality, complete penetrance	Nsdhl<Str-1Or>/Nsdhl<Str-1Or>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3590090	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Nsdhl<Str-2H>/Y	involves: 101/H * C3H/HeH	N	10369263
MGI:3590090	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Nsdhl<Str-2H>/Y	involves: 101/H * C3H/HeH	N	15639195
MGI:3590091	F	MP:0002940	variable body spotting	Nsdhl<Str-2H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590091	F	MP:0000372	irregular coat pigmentation	Nsdhl<Str-2H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590094	M	MP:0011091	prenatal lethality, complete penetrance	Nsdhl<Bpa-3H>/Y	involves: 101/H * C3H/HeH	N	10369263
MGI:3590095	F	MP:0000418	focal hair loss	Nsdhl<Bpa-3H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	MGI:3044155
MGI:3590095	F	MP:0004703	abnormal vertebral column morphology	Nsdhl<Bpa-3H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	MGI:3044155
MGI:3590095	F	MP:0001242	hyperkeratosis	Nsdhl<Bpa-3H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590095	F	MP:0005508	abnormal skeleton morphology	Nsdhl<Bpa-3H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590095	F	MP:0000372	irregular coat pigmentation	Nsdhl<Bpa-3H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590095	F	MP:0001191	abnormal skin condition	Nsdhl<Bpa-3H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	MGI:3044155
MGI:3590125	F	MP:0000414	alopecia	Nsdhl<Bpa-4H>/Nsdhl<+>	Not Specified	N	MGI:3044155
MGI:3590125	F	MP:0004703	abnormal vertebral column morphology	Nsdhl<Bpa-4H>/Nsdhl<+>	Not Specified	N	MGI:3044155
MGI:3590126	M	MP:0011091	prenatal lethality, complete penetrance	Nsdhl<Bpa-4H>/Y	Not Specified	N	MGI:3044155
MGI:3590127	F	MP:0000372	irregular coat pigmentation	Nsdhl<Bpa-5H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590127	F	MP:0005508	abnormal skeleton morphology	Nsdhl<Bpa-5H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590127	F	MP:0000418	focal hair loss	Nsdhl<Bpa-5H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	MGI:3044155
MGI:3590127	F	MP:0001242	hyperkeratosis	Nsdhl<Bpa-5H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590127	F	MP:0004704	short vertebral column	Nsdhl<Bpa-5H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	MGI:3044155
MGI:3590127	F	MP:0001265	decreased body size	Nsdhl<Bpa-5H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	MGI:3044155
MGI:3590128	M	MP:0011091	prenatal lethality, complete penetrance	Nsdhl<Bpa-5H>/Y	involves: 101/H * C3H/HeH	N	10369263
MGI:3590129	M	MP:0011091	prenatal lethality, complete penetrance	Nsdhl<Bpa-6H>/Y	involves: 101/H * C3H/HeH	N	10369263
MGI:3590130	F	MP:0001242	hyperkeratosis	Nsdhl<Bpa-6H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590130	F	MP:0000418	focal hair loss	Nsdhl<Bpa-6H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	MGI:3044155
MGI:3590130	F	MP:0005508	abnormal skeleton morphology	Nsdhl<Bpa-6H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590130	F	MP:0000372	irregular coat pigmentation	Nsdhl<Bpa-6H>/Nsdhl<+>	involves: 101/H * C3H/HeH	N	10369263
MGI:3590150	F	MP:0001923	reduced female fertility	Ptger2<tm1Sna>/Ptger2<tm1Sna>	involves: 129P2/OlaHsd * C57BL/6	N	10468638
MGI:3590150	F	MP:0009373	abnormal cumulus expansion	Ptger2<tm1Sna>/Ptger2<tm1Sna>	involves: 129P2/OlaHsd * C57BL/6	N	9751056
MGI:3590150	F	MP:0009374	absent cumulus expansion	Ptger2<tm1Sna>/Ptger2<tm1Sna>	involves: 129P2/OlaHsd * C57BL/6	N	10468638
MGI:3590150	F	MP:0003355	decreased ovulation rate	Ptger2<tm1Sna>/Ptger2<tm1Sna>	involves: 129P2/OlaHsd * C57BL/6	N	10468638
MGI:3590150	F	MP:0002680	decreased corpora lutea number	Ptger2<tm1Sna>/Ptger2<tm1Sna>	involves: 129P2/OlaHsd * C57BL/6	N	10468638
MGI:3590150	F	MP:0001125	abnormal oocyte morphology	Ptger2<tm1Sna>/Ptger2<tm1Sna>	involves: 129P2/OlaHsd * C57BL/6	N	10468638
MGI:3590155	F	MP:0008047	absent uterine NK cells	Il15<tm1Imx>/Il15<tm1Imx>	involves: C57BL/6	N	12816981
MGI:3590155	F	MP:0003845	abnormal decidualization	Il15<tm1Imx>/Il15<tm1Imx>	involves: C57BL/6	N	12816981
MGI:3590155	F	MP:0003995	abnormal uterine artery morphology	Il15<tm1Imx>/Il15<tm1Imx>	involves: C57BL/6	N	12816981
MGI:3590196	M	MP:0008545	absent sperm flagellum	repro28/repro28	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590196	M	MP:0002675	asthenozoospermia	repro28/repro28	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590196	M	MP:0001932	abnormal spermiogenesis	repro28/repro28	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590196	M	MP:0002686	globozoospermia	repro28/repro28	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590196	M	MP:0004910	decreased seminal vesicle weight	repro28/repro28	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590196	M	MP:0009237	kinked sperm flagellum	repro28/repro28	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590196	M	MP:0001925	male infertility	repro28/repro28	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590196	M	MP:0002687	oligozoospermia	repro28/repro28	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590200	M	MP:0002675	asthenozoospermia	Ccdc62<repro29>/Ccdc62<repro29>	involves: C3HeB/FeJ * C57BL/6J	N	28339613
MGI:3590200	M	MP:0004910	decreased seminal vesicle weight	Ccdc62<repro29>/Ccdc62<repro29>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590200	M	MP:0001925	male infertility	Ccdc62<repro29>/Ccdc62<repro29>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590200	M	MP:0008839	absent acrosome	Ccdc62<repro29>/Ccdc62<repro29>	involves: C3HeB/FeJ * C57BL/6J	N	28339613
MGI:3590200	M	MP:0002687	oligozoospermia	Ccdc62<repro29>/Ccdc62<repro29>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590200	M	MP:0002675	asthenozoospermia	Ccdc62<repro29>/Ccdc62<repro29>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590200	M	MP:0001932	abnormal spermiogenesis	Ccdc62<repro29>/Ccdc62<repro29>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590200	M	MP:0005578	teratozoospermia	Ccdc62<repro29>/Ccdc62<repro29>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590200	M	MP:0005578	teratozoospermia	Ccdc62<repro29>/Ccdc62<repro29>	involves: C3HeB/FeJ * C57BL/6J	N	28339613
MGI:3590200	M	MP:0009831	abnormal sperm midpiece morphology	Ccdc62<repro29>/Ccdc62<repro29>	involves: C3HeB/FeJ * C57BL/6J	N	28339613
MGI:3590200	M	MP:0001925	male infertility	Ccdc62<repro29>/Ccdc62<repro29>	involves: C3HeB/FeJ * C57BL/6J	N	28339613
MGI:3590200	M	MP:0009230	abnormal sperm head morphology	Ccdc62<repro29>/Ccdc62<repro29>	involves: C3HeB/FeJ * C57BL/6J	N	28339613
MGI:3590202	M	MP:0006380	abnormal spermatid morphology	repro31/repro31	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590202	F	MP:0001926	female infertility	repro31/repro31	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590202	M	MP:0002674	abnormal sperm motility	repro31/repro31	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590202	M	MP:0004910	decreased seminal vesicle weight	repro31/repro31	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590202	M	MP:0006362	abnormal male germ cell morphology	repro31/repro31	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590202	M	MP:0001925	male infertility	repro31/repro31	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590202	M	MP:0002673	abnormal sperm number	repro31/repro31	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590203	M	MP:0004910	decreased seminal vesicle weight	repro33/repro33	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590203	M	MP:0001925	male infertility	repro33/repro33	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590203	M	MP:0002673	abnormal sperm number	repro33/repro33	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590203	M	MP:0002674	abnormal sperm motility	repro33/repro33	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590203	M	MP:0006362	abnormal male germ cell morphology	repro33/repro33	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590204	M	MP:0001925	male infertility	Capza3<repro32>/Capza3<repro32>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590204	M	MP:0008892	abnormal sperm flagellum morphology	Capza3<repro32>/Capza3<repro32>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590204	M	MP:0009230	abnormal sperm head morphology	Capza3<repro32>/Capza3<repro32>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590204	M	MP:0002687	oligozoospermia	Capza3<repro32>/Capza3<repro32>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590204	M	MP:0001932	abnormal spermiogenesis	Capza3<repro32>/Capza3<repro32>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590204	M	MP:0002675	asthenozoospermia	Capza3<repro32>/Capza3<repro32>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3590677	F	MP:0002961	abnormal axon guidance	Plxna3<tm1Matl>/Plxna3<tm1Matl>,Plxna4<tm1Matl>/Plxna4<tm1Matl>	either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)	N	15721238
MGI:3590677	F	MP:0000968	abnormal sensory neuron innervation pattern	Plxna3<tm1Matl>/Plxna3<tm1Matl>,Plxna4<tm1Matl>/Plxna4<tm1Matl>	either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)	N	15721238
MGI:3590677	F	MP:0001063	abnormal trochlear nerve morphology	Plxna3<tm1Matl>/Plxna3<tm1Matl>,Plxna4<tm1Matl>/Plxna4<tm1Matl>	either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)	N	15721238
MGI:3590677	F	MP:0001065	abnormal trigeminal nerve morphology	Plxna3<tm1Matl>/Plxna3<tm1Matl>,Plxna4<tm1Matl>/Plxna4<tm1Matl>	either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)	N	15721238
MGI:3603005	F	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance	Tsix<tm1Enl>/Tsix<+>,Xist<tm1Sado>/Xist<+>	involves: 129S4/SvJae	N	15992549
MGI:3603115	F	MP:0009011	prolonged diestrus	Scd1<ab>/Scd1<ab>	involves: BALB/cCrglGa	N	17738154
MGI:3603115	F	MP:0001923	reduced female fertility	Scd1<ab>/Scd1<ab>	involves: BALB/cCrglGa	N	17738154
MGI:3603115	F	MP:0001927	abnormal estrous cycle	Scd1<ab>/Scd1<ab>	involves: BALB/cCrglGa	N	17738154
MGI:3603330	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Trp53<tm1Thl>/Trp53<tm1Thl>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	16079851
MGI:3603337	M	MP:0001925	male infertility	Kit<tm1Bpr>/Kit<tm1Bpr>	either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	N	16061643
MGI:3603337	M	MP:0001152	increased Leydig cell number	Kit<tm1Bpr>/Kit<tm1Bpr>	either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	N	16061643
MGI:3603337	F	MP:0004805	absent oocytes	Kit<tm1Bpr>/Kit<tm1Bpr>	either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	N	16061643
MGI:3603337	F	MP:0001127	small ovary	Kit<tm1Bpr>/Kit<tm1Bpr>	either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	N	16061643
MGI:3603337	M	MP:0005159	azoospermia	Kit<tm1Bpr>/Kit<tm1Bpr>	either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	N	16061643
MGI:3603337	F	MP:0001126	abnormal ovary morphology	Kit<tm1Bpr>/Kit<tm1Bpr>	either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	N	16061643
MGI:3603337	M	MP:0002216	abnormal seminiferous tubule morphology	Kit<tm1Bpr>/Kit<tm1Bpr>	either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	N	16061643
MGI:3603337	F	MP:0001926	female infertility	Kit<tm1Bpr>/Kit<tm1Bpr>	either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	N	16061643
MGI:3603412	F	MP:0006270	abnormal mammary gland growth during lactation	Oxt<tm1Wsy>/Oxt<tm1Wsy>	involves: 129S/SvEv * C57BL/6	N	10026810
MGI:3603412	M	MP:0005367	renal/urinary system phenotype	Oxt<tm1Wsy>/Oxt<tm1Wsy>	involves: 129S/SvEv * C57BL/6	Y	8933362
MGI:3603412	F	MP:0001882	abnormal lactation	Oxt<tm1Wsy>/Oxt<tm1Wsy>	involves: 129S/SvEv * C57BL/6	N	8933362
MGI:3603412	F	MP:0001882	abnormal lactation	Oxt<tm1Wsy>/Oxt<tm1Wsy>	involves: 129S/SvEv * C57BL/6	N	10026810
MGI:3603412	M	MP:0020467	abnormal circadian behavior	Oxt<tm1Wsy>/Oxt<tm1Wsy>	involves: 129S/SvEv * C57BL/6	N	11573985
MGI:3603412	F	MP:0013718	galactostasis	Oxt<tm1Wsy>/Oxt<tm1Wsy>	involves: 129S/SvEv * C57BL/6	N	8933362
MGI:3603412	F	MP:0013718	galactostasis	Oxt<tm1Wsy>/Oxt<tm1Wsy>	involves: 129S/SvEv * C57BL/6	N	10026810
MGI:3603412	M	MP:0001422	abnormal drinking behavior	Oxt<tm1Wsy>/Oxt<tm1Wsy>	involves: 129S/SvEv * C57BL/6	N	11573985
MGI:3603425	F	MP:0012008	delayed parturition	Ptgs1<tm1Unc>/Ptgs1<tm1Unc>,Oxt<tm1Ljm>/Oxt<tm1Ljm>	involves: 129P2/OlaHsd * C57BL/6	N	9751758
MGI:3603425	F	MP:0010249	lactation failure	Ptgs1<tm1Unc>/Ptgs1<tm1Unc>,Oxt<tm1Ljm>/Oxt<tm1Ljm>	involves: 129P2/OlaHsd * C57BL/6	N	9751758
MGI:3603529	M	MP:0001155	arrest of spermatogenesis	Rxfp2<tm1Aia>/crsp	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	12217959
MGI:3603529	M	MP:0001925	male infertility	Rxfp2<tm1Aia>/crsp	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	12217959
MGI:3603529	M	MP:0031287	bilateral cryptorchism	Rxfp2<tm1Aia>/crsp	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	12217959
MGI:3603529	M	MP:0001147	small testis	Rxfp2<tm1Aia>/crsp	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	12217959
MGI:3603529	M	MP:0009213	absent male inguinal canal	Rxfp2<tm1Aia>/crsp	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	12217959
MGI:3603529	M	MP:0005159	azoospermia	Rxfp2<tm1Aia>/crsp	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	12217959
MGI:3603536	F	MP:0001923	reduced female fertility	Lbr<ic>/Lbr<ic>	Not Specified	N	MGI:61274
MGI:3603536	F	MP:0001143	constricted vagina orifice	Lbr<ic>/Lbr<ic>	Not Specified	N	MGI:61274
MGI:3603536	M	MP:0002286	cryptorchism	Lbr<ic>/Lbr<ic>	Not Specified	N	MGI:61274
MGI:3603536	M	MP:0001925	male infertility	Lbr<ic>/Lbr<ic>	Not Specified	N	MGI:61274
MGI:3603537	F	MP:0008868	abnormal granulosa cell morphology	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	N	11356696
MGI:3603537	F	MP:0031239	increased atretic ovarian follicle number	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	N	11356696
MGI:3603795	F	MP:0001382	abnormal nursing	Oxt<tm1Zuk>/Oxt<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	8876199
MGI:3603795	F	MP:0003838	abnormal milk ejection	Oxt<tm1Zuk>/Oxt<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	8876199
MGI:3603798	M	MP:0002359	abnormal spleen germinal center morphology	Cd19<tm1(cre)Cgn>/Cd19<+>,Igbp1<tm1Imku>/Y	involves: 129P2/OlaHsd	N	11809737
MGI:3603798	M	MP:0008209	decreased pre-B cell number	Cd19<tm1(cre)Cgn>/Cd19<+>,Igbp1<tm1Imku>/Y	involves: 129P2/OlaHsd	N	11809737
MGI:3603798	M	MP:0004815	abnormal somatic hypermutation frequency	Cd19<tm1(cre)Cgn>/Cd19<+>,Igbp1<tm1Imku>/Y	involves: 129P2/OlaHsd	N	11809737
MGI:3603798	M	MP:0008174	decreased follicular B cell number	Cd19<tm1(cre)Cgn>/Cd19<+>,Igbp1<tm1Imku>/Y	involves: 129P2/OlaHsd	N	11809737
MGI:3603798	M	MP:0002460	decreased immunoglobulin level	Cd19<tm1(cre)Cgn>/Cd19<+>,Igbp1<tm1Imku>/Y	involves: 129P2/OlaHsd	N	11809737
MGI:3603798	M	MP:0005017	decreased B cell number	Cd19<tm1(cre)Cgn>/Cd19<+>,Igbp1<tm1Imku>/Y	involves: 129P2/OlaHsd	N	11809737
MGI:3603798	M	MP:0002459	abnormal B cell physiology	Cd19<tm1(cre)Cgn>/Cd19<+>,Igbp1<tm1Imku>/Y	involves: 129P2/OlaHsd	N	11809737
MGI:3603798	M	MP:0005093	decreased B cell proliferation	Cd19<tm1(cre)Cgn>/Cd19<+>,Igbp1<tm1Imku>/Y	involves: 129P2/OlaHsd	N	11809737
MGI:3603799	M	MP:0005089	decreased double-negative T cell number	Igbp1<tm1Imku>/Y,Tg(Lck-cre)I57Jxm/?	involves: 129P2/OlaHsd * ICR	N	12811850
MGI:3603799	M	MP:0002371	abnormal thymus cortex morphology	Igbp1<tm1Imku>/Y,Tg(Lck-cre)I57Jxm/?	involves: 129P2/OlaHsd * ICR	N	12811850
MGI:3603799	M	MP:0009543	abnormal thymus corticomedullary boundary morphology	Igbp1<tm1Imku>/Y,Tg(Lck-cre)I57Jxm/?	involves: 129P2/OlaHsd * ICR	N	12811850
MGI:3603799	M	MP:0005018	decreased T cell number	Igbp1<tm1Imku>/Y,Tg(Lck-cre)I57Jxm/?	involves: 129P2/OlaHsd * ICR	N	12811850
MGI:3603799	M	MP:0000715	decreased thymocyte number	Igbp1<tm1Imku>/Y,Tg(Lck-cre)I57Jxm/?	involves: 129P2/OlaHsd * ICR	N	12811850
MGI:3603831	F	MP:0001926	female infertility	Ptgs2<tm1Unc>/Ptgs2<tm1Unc>	D1.129P2(B6J)-Ptgs2<tm1Unc>	N	10954756
MGI:3603952	F	MP:0031420	decreased superovulation rate	Ptgs2<tm1Jed>/Ptgs2<tm1Jed>	involves: 129S7/SvEvBrd * C57BL/6	N	11319164
MGI:3603952	F	MP:0003845	abnormal decidualization	Ptgs2<tm1Jed>/Ptgs2<tm1Jed>	involves: 129S7/SvEvBrd * C57BL/6	N	9346237
MGI:3603952	F	MP:0012737	abnormal primary polar body morphology	Ptgs2<tm1Jed>/Ptgs2<tm1Jed>	involves: 129S7/SvEvBrd * C57BL/6	N	9346237
MGI:3603952	F	MP:0001923	reduced female fertility	Ptgs2<tm1Jed>/Ptgs2<tm1Jed>	involves: 129S7/SvEvBrd * C57BL/6	N	16732282
MGI:3603952	F	MP:0001728	failure of embryo implantation	Ptgs2<tm1Jed>/Ptgs2<tm1Jed>	involves: 129S7/SvEvBrd * C57BL/6	N	9346237
MGI:3603952	F	MP:0031420	decreased superovulation rate	Ptgs2<tm1Jed>/Ptgs2<tm1Jed>	involves: 129S7/SvEvBrd * C57BL/6	N	9346237
MGI:3603952	F	MP:0001923	reduced female fertility	Ptgs2<tm1Jed>/Ptgs2<tm1Jed>	involves: 129S7/SvEvBrd * C57BL/6	N	17110378
MGI:3604026	F	MP:0000662	abnormal branching of the mammary ductal tree	Id2<tm1Yyk>/Id2<tm1Yyk>	involves: 129S1/Sv * 129X1/SvJ	N	15601467
MGI:3604027	F	MP:0001882	abnormal lactation	Id2<tm1Yyk>/Id2<tm1Yyk>	involves: 129S1/Sv * 129X1/SvJ * NMRI	N	10067894
MGI:3604027	F	MP:0006269	abnormal mammary gland growth during pregnancy	Id2<tm1Yyk>/Id2<tm1Yyk>	involves: 129S1/Sv * 129X1/SvJ * NMRI	N	11060028
MGI:3604027	F	MP:0001882	abnormal lactation	Id2<tm1Yyk>/Id2<tm1Yyk>	involves: 129S1/Sv * 129X1/SvJ * NMRI	N	11060028
MGI:3604078	M	MP:0001922	reduced male fertility	Fgfr2<tm2Cxd>/Fgfr2<+>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S6/SvEvTac * FVB/N	N	14499350
MGI:3604078	F	MP:0001926	female infertility	Fgfr2<tm2Cxd>/Fgfr2<+>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S6/SvEvTac * FVB/N	N	14499350
MGI:3604219	F	MP:0000877	abnormal Purkinje cell morphology	Fmr1<tm1.1Cidz>/Fmr1<tm1.1Cidz>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129X1/SvJ	N	16055059
MGI:3604219	F	MP:0002807	abnormal eye blink conditioning behavior	Fmr1<tm1.1Cidz>/Fmr1<tm1.1Cidz>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129X1/SvJ	N	16055059
MGI:3604219	F	MP:0001898	abnormal long-term depression	Fmr1<tm1.1Cidz>/Fmr1<tm1.1Cidz>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129X1/SvJ	N	16055059
MGI:3604354	F	MP:0008054	abnormal uterine NK cell morphology	Il11ra1<tm1Gos>/Il11ra1<tm1Gos>	involves: 129S2/SvPas * C57BL/6J * CD-1	N	15499555
MGI:3604354	F	MP:0001926	female infertility	Il11ra1<tm1Gos>/Il11ra1<tm1Gos>	involves: 129S2/SvPas * C57BL/6J * CD-1	N	15499555
MGI:3604354	F	MP:0003845	abnormal decidualization	Il11ra1<tm1Gos>/Il11ra1<tm1Gos>	involves: 129S2/SvPas * C57BL/6J * CD-1	N	15499555
MGI:3604405	F	MP:0003845	abnormal decidualization	Il11ra1<tm1Wehi>/Il11ra1<tm1Wehi>	either: (involves: 129S1/Sv) or (involves: 129S1/Sv * C57BL/6)	N	9500603
MGI:3604405	F	MP:0001729	impaired embryo implantation	Il11ra1<tm1Wehi>/Il11ra1<tm1Wehi>	either: (involves: 129S1/Sv) or (involves: 129S1/Sv * C57BL/6)	N	9500603
MGI:3604722	M	MP:0001922	reduced male fertility	Dido1<tm1Cmar>/Dido1<tm1Cmar>	involves: 129S1/Sv * 129X1/SvJ	N	16127461
MGI:3604722	F	MP:0001923	reduced female fertility	Dido1<tm1Cmar>/Dido1<tm1Cmar>	involves: 129S1/Sv * 129X1/SvJ	N	16127461
MGI:3604811	M	MP:0001925	male infertility	Map3k4<tm1Glj>/Map3k4<tm1Glj>	involves: 129S6/SvEvTac * C57BL/6	N	16199873
MGI:3604811	M	MP:0002687	oligozoospermia	Map3k4<tm1Glj>/Map3k4<tm1Glj>	involves: 129S6/SvEvTac * C57BL/6	N	16199873
MGI:3604811	M	MP:0002675	asthenozoospermia	Map3k4<tm1Glj>/Map3k4<tm1Glj>	involves: 129S6/SvEvTac * C57BL/6	N	16199873
MGI:3605005	M	MP:0001925	male infertility	Hydin<hy3>/Hydin<hy3>	involves: CBA	N	MGI:61244
MGI:3605232	F	MP:0001382	abnormal nursing	Efna3<tm1Rax>/Efna3<tm1Rax>,Efna5<tm1Ddmo>/Efna5<tm1Ddmo>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	12914696
MGI:3605638	M	MP:0006262	increased testis tumor incidence	Tgct1<MOLF/Ei>/Tgct1<MOLF/Ei>	involves: 129S1/SvImJ * MOLF/Ei	N	12566386
MGI:3605639	M	MP:0006262	increased testis tumor incidence	Tgct2<MOLF/Ei>/Tgct2<MOLF/Ei>	involves: 129S1/SvImJ * MOLF/Ei	N	12566386
MGI:3605640	M	MP:0006262	increased testis tumor incidence	Tgct3<MOLF/Ei>/Tgct3<MOLF/Ei>	involves: 129S1/SvImJ * MOLF/Ei	N	12566386
MGI:3605642	M	MP:0006262	increased testis tumor incidence	Tgct5<MOLF/Ei>/Tgct5<MOLF/Ei>	involves: 129S1/SvImJ * MOLF/Ei	N	12566386
MGI:3605643	M	MP:0009230	abnormal sperm head morphology	Spha1<MSM/Ms>/Spha1<MSM/Ms>	involves: C57BL/6J * MSM/Ms	N	15020476
MGI:3605644	M	MP:0009230	abnormal sperm head morphology	Spha2<MSM/Ms>/Spha2<MSM/Ms>	involves: C57BL/6J * MSM/Ms	N	15020476
MGI:3605645	M	MP:0009230	abnormal sperm head morphology	Spha3<MSM/Ms>/Spha3<MSM/Ms>	involves: C57BL/6J * MSM/Ms	N	15020476
MGI:3605769	M	MP:0001147	small testis	Htt<tm1Szi>/Htt<tm2Szi>,Tg(Camk2a-cre)1Szi/0	involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA	N	11062468
MGI:3605769	M	MP:0001922	reduced male fertility	Htt<tm1Szi>/Htt<tm2Szi>,Tg(Camk2a-cre)1Szi/0	involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA	N	11062468
MGI:3605769	M	MP:0002687	oligozoospermia	Htt<tm1Szi>/Htt<tm2Szi>,Tg(Camk2a-cre)1Szi/0	involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA	N	11062468
MGI:3605769	M	MP:0002216	abnormal seminiferous tubule morphology	Htt<tm1Szi>/Htt<tm2Szi>,Tg(Camk2a-cre)1Szi/0	involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA	N	11062468
MGI:3605770	M	MP:0001147	small testis	Htt<tm1Szi>/Htt<tm2Szi>,Tg(Camk2a-cre)2Szi/0	involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA	N	11062468
MGI:3605770	M	MP:0002216	abnormal seminiferous tubule morphology	Htt<tm1Szi>/Htt<tm2Szi>,Tg(Camk2a-cre)2Szi/0	involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA	N	11062468
MGI:3605770	M	MP:0001922	reduced male fertility	Htt<tm1Szi>/Htt<tm2Szi>,Tg(Camk2a-cre)2Szi/0	involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA	N	11062468
MGI:3605770	M	MP:0002687	oligozoospermia	Htt<tm1Szi>/Htt<tm2Szi>,Tg(Camk2a-cre)2Szi/0	involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA	N	11062468
MGI:3605828	F	MP:0000628	abnormal mammary gland development	Cebpb<tm1Vpo>/Cebpb<tm1Vpo>	involves: 129S/SvEv * C57BL/6 * MF1	N	9637692
MGI:3605828	F	MP:0001926	female infertility	Cebpb<tm1Vpo>/Cebpb<tm1Vpo>	involves: 129S/SvEv * C57BL/6 * MF1	N	9637692
MGI:3605828	F	MP:0009503	abnormal mammary gland duct morphology	Cebpb<tm1Vpo>/Cebpb<tm1Vpo>	involves: 129S/SvEv * C57BL/6 * MF1	N	9637692
MGI:3605828	F	MP:0010172	abnormal mammary gland epithelium physiology	Cebpb<tm1Vpo>/Cebpb<tm1Vpo>	involves: 129S/SvEv * C57BL/6 * MF1	N	9637692
MGI:3605828	F	MP:0000662	abnormal branching of the mammary ductal tree	Cebpb<tm1Vpo>/Cebpb<tm1Vpo>	involves: 129S/SvEv * C57BL/6 * MF1	N	9637692
MGI:3605829	F	MP:0009503	abnormal mammary gland duct morphology	Cebpb<tm1Vpo>/Cebpb<+>	involves: 129S/SvEv * C57BL/6 * MF1	N	9637692
MGI:3606085	F	MP:0003699	abnormal female reproductive system physiology	Prf1<tm1Sdz>/Prf1<tm1Sdz>	C57BL/6-Prf1<tm1Sdz>	N	10639149
MGI:3606086	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Dusp9<tm1Skey>/Dusp9<+>	involves: 129P2/OlaHsd * C57BL/6J	N	16135819
MGI:3606086	F	MP:0004255	abnormal spongiotrophoblast layer morphology	Dusp9<tm1Skey>/Dusp9<+>	involves: 129P2/OlaHsd * C57BL/6J	N	16135819
MGI:3606086	F	MP:0001716	abnormal placenta labyrinth morphology	Dusp9<tm1Skey>/Dusp9<+>	involves: 129P2/OlaHsd * C57BL/6J	N	16135819
MGI:3606088	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Dusp9<tm1Skey>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	16135819
MGI:3606088	M	MP:0001716	abnormal placenta labyrinth morphology	Dusp9<tm1Skey>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	16135819
MGI:3606088	M	MP:0004255	abnormal spongiotrophoblast layer morphology	Dusp9<tm1Skey>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	16135819
MGI:3606089	M	MP:0005159	azoospermia	Slc19a2<tm1Ejn>/Slc19a2<tm1Ejn>	involves: 129S4/SvJae * 129S6/SvEvTac	N	14567973
MGI:3606089	M	MP:0001147	small testis	Slc19a2<tm1Ejn>/Slc19a2<tm1Ejn>	involves: 129S4/SvJae * 129S6/SvEvTac	N	14567973
MGI:3606089	M	MP:0008261	arrest of male meiosis	Slc19a2<tm1Ejn>/Slc19a2<tm1Ejn>	involves: 129S4/SvJae * 129S6/SvEvTac	N	14567973
MGI:3606089	M	MP:0001925	male infertility	Slc19a2<tm1Ejn>/Slc19a2<tm1Ejn>	involves: 129S4/SvJae * 129S6/SvEvTac	N	14567973
MGI:3606112	M	MP:0006380	abnormal spermatid morphology	Hsd17b4<tm1Baes>/Hsd17b4<tm1Baes>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3606112	M	MP:0001922	reduced male fertility	Hsd17b4<tm1Baes>/Hsd17b4<tm1Baes>	involves: 129S1/Sv * 129X1/SvJ	N	10748062
MGI:3606112	M	MP:0001147	small testis	Hsd17b4<tm1Baes>/Hsd17b4<tm1Baes>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3606112	M	MP:0002216	abnormal seminiferous tubule morphology	Hsd17b4<tm1Baes>/Hsd17b4<tm1Baes>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3606112	M	MP:0006362	abnormal male germ cell morphology	Hsd17b4<tm1Baes>/Hsd17b4<tm1Baes>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3606112	M	MP:0001156	abnormal spermatogenesis	Hsd17b4<tm1Baes>/Hsd17b4<tm1Baes>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3606112	M	MP:0002631	abnormal epididymis morphology	Hsd17b4<tm1Baes>/Hsd17b4<tm1Baes>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3606112	M	MP:0001146	abnormal testis morphology	Hsd17b4<tm1Baes>/Hsd17b4<tm1Baes>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3606112	M	MP:0001925	male infertility	Hsd17b4<tm1Baes>/Hsd17b4<tm1Baes>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3606112	M	MP:0001154	seminiferous tubule degeneration	Hsd17b4<tm1Baes>/Hsd17b4<tm1Baes>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3606112	M	MP:0001145	abnormal male reproductive system morphology	Hsd17b4<tm1Baes>/Hsd17b4<tm1Baes>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3606146	F	MP:0001926	female infertility	Hsf1<tm1Ijb>/Hsf1<tm1Ijb>	either: (involves: 129S6/SvEvTac * 129X1/SvJ) or (involves: 129S6/SvEvTac * BALB/c) or (involves: 129S6/SvEvTac * C57BL/6J) or (involves: 129S6/SvEvTac * ICR)	N	11048707
MGI:3606146	F	MP:0001926	female infertility	Hsf1<tm1Ijb>/Hsf1<tm1Ijb>	either: (involves: 129S6/SvEvTac * 129X1/SvJ) or (involves: 129S6/SvEvTac * BALB/c) or (involves: 129S6/SvEvTac * C57BL/6J) or (involves: 129S6/SvEvTac * ICR)	N	10545106
MGI:3606183	M	MP:0001147	small testis	Rnf17<tm1Jw>/Rnf17<tm1Jw>	involves: 129 * C57BL/6	N	16093322
MGI:3606183	M	MP:0001153	small seminiferous tubules	Rnf17<tm1Jw>/Rnf17<tm1Jw>	involves: 129 * C57BL/6	N	16093322
MGI:3606183	M	MP:0001155	arrest of spermatogenesis	Rnf17<tm1Jw>/Rnf17<tm1Jw>	involves: 129 * C57BL/6	N	16093322
MGI:3606183	M	MP:0001925	male infertility	Rnf17<tm1Jw>/Rnf17<tm1Jw>	involves: 129 * C57BL/6	N	16093322
MGI:3606183	M	MP:0005159	azoospermia	Rnf17<tm1Jw>/Rnf17<tm1Jw>	involves: 129 * C57BL/6	N	16093322
MGI:3606450	F	MP:0001262	decreased body weight	Gria3<tm1Dgen>/Gria3<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3606564	M	MP:0004929	decreased epididymis weight	Adipor2<tm1Dgen>/Adipor2<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3606564	M	MP:0001154	seminiferous tubule degeneration	Adipor2<tm1Dgen>/Adipor2<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3606564	M	MP:0020550	multinucleated giant male germ cells	Adipor2<tm1Dgen>/Adipor2<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3606564	M	MP:0004852	decreased testis weight	Adipor2<tm1Dgen>/Adipor2<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3606564	M	MP:0001156	abnormal spermatogenesis	Adipor2<tm1Dgen>/Adipor2<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3606564	M	MP:0002687	oligozoospermia	Adipor2<tm1Dgen>/Adipor2<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3606617	F	MP:0002169	no abnormal phenotype detected	Mtmr1<tm1Dgen>/Mtmr1<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3606913	F	MP:0003724	increased susceptibility to induced arthritis	Pgia39<DBA/2Crl>/Pgia39<DBA/2Crl>,Pgia26<BALB/cCrl>/Pgia26<BALB/cCrl>	involves: BALB/cCrl * DBA/2Crl	N	12794840
MGI:3606915	F	MP:0003724	increased susceptibility to induced arthritis	Pgia39<DBA/2Crl>/Pgia39<DBA/2Crl>,Pgia6<DBA/2Crl>/Pgia6<DBA/2Crl>	involves: BALB/cCrl * DBA/2Crl	N	12794840
MGI:3607320	M	MP:0031352	absent sperm axonemal central pair	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607320	M	MP:0009838	abnormal sperm axoneme morphology	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607320	M	MP:0001155	arrest of spermatogenesis	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607320	M	MP:0009237	kinked sperm flagellum	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607320	M	MP:0014052	increased male germ cell apoptosis	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607320	M	MP:0002216	abnormal seminiferous tubule morphology	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607320	M	MP:0001156	abnormal spermatogenesis	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607320	M	MP:0031356	abnormal outer dense fiber morphology	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607320	M	MP:0002674	abnormal sperm motility	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607320	M	MP:0002687	oligozoospermia	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607320	M	MP:0002784	abnormal Sertoli cell morphology	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607320	M	MP:0001925	male infertility	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607320	M	MP:0001154	seminiferous tubule degeneration	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607320	M	MP:0001147	small testis	Spag16<tm1Jfs>/Spag16<+>	chimera involves: 129/Sv * C57BL/6J	N	15328412
MGI:3607451	M	MP:0001925	male infertility	Nectin3<tm1Ytk>/Nectin3<tm1Ytk>	either: (involves: 129X1/SvJ * C57BL * DBA) or (involves: 129X1/SvJ * BALB/cA * C57BL * DBA)	N	15728677
MGI:3607508	F	MP:0005168	abnormal female meiosis	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	N	12714746
MGI:3607508	M	MP:0008261	arrest of male meiosis	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	N	12714746
MGI:3607508	M	MP:0003205	testicular atrophy	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	N	12714746
MGI:3607508	M	MP:0001925	male infertility	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	N	12714746
MGI:3607508	M	MP:0020550	multinucleated giant male germ cells	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	N	12714746
MGI:3607508	F	MP:0001926	female infertility	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	N	12714746
MGI:3607508	M	MP:0005159	azoospermia	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	N	12714746
MGI:3607702	F	MP:0005168	abnormal female meiosis	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	N	11702780
MGI:3607702	M	MP:0014052	increased male germ cell apoptosis	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	N	11702780
MGI:3607702	M	MP:0002687	oligozoospermia	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	N	11702780
MGI:3607702	F	MP:0003582	abnormal ovary development	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	N	11702780
MGI:3607702	F	MP:0003578	absent ovary	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	N	11702780
MGI:3607702	M	MP:0004852	decreased testis weight	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	N	11702780
MGI:3607702	M	MP:0001922	reduced male fertility	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	N	11702780
MGI:3607702	F	MP:0001926	female infertility	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	N	11702780
MGI:3607702	M	MP:0008261	arrest of male meiosis	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	N	11702780
MGI:3608124	M	MP:0002784	abnormal Sertoli cell morphology	Rxrb<tm1Mma>/Rxrb<tm1Mma>	involves: 129 * C57BL/6	N	14993927
MGI:3608127	M	MP:0002784	abnormal Sertoli cell morphology	Nr1h2<tm1.1Gstr>/Nr1h2<+>,Rxrb<tm1Mma>/Rxrb<+>	involves: 129 * C57BL/6	N	14993927
MGI:3608128	M	MP:0002784	abnormal Sertoli cell morphology	Nr1h2<tm1.1Gstr>/Nr1h2<tm1.1Gstr>	involves: 129 * C57BL/6	N	14993927
MGI:3608130	M	MP:0004852	decreased testis weight	Ncoa2<tm1.2Ipc>/Ncoa2<tm1.2Ipc>	involves: 129S2/SvPas * C57BL/6	N	12138202
MGI:3608130	M	MP:0002216	abnormal seminiferous tubule morphology	Ncoa2<tm1.2Ipc>/Ncoa2<tm1.2Ipc>	involves: 129S2/SvPas * C57BL/6	N	12138202
MGI:3608130	M	MP:0002784	abnormal Sertoli cell morphology	Ncoa2<tm1.2Ipc>/Ncoa2<tm1.2Ipc>	involves: 129S2/SvPas * C57BL/6	N	14993927
MGI:3608130	M	MP:0002784	abnormal Sertoli cell morphology	Ncoa2<tm1.2Ipc>/Ncoa2<tm1.2Ipc>	involves: 129S2/SvPas * C57BL/6	N	12138202
MGI:3608130	M	MP:0001146	abnormal testis morphology	Ncoa2<tm1.2Ipc>/Ncoa2<tm1.2Ipc>	involves: 129S2/SvPas * C57BL/6	N	12138202
MGI:3608130	F	MP:0001923	reduced female fertility	Ncoa2<tm1.2Ipc>/Ncoa2<tm1.2Ipc>	involves: 129S2/SvPas * C57BL/6	N	12138202
MGI:3608130	M	MP:0001922	reduced male fertility	Ncoa2<tm1.2Ipc>/Ncoa2<tm1.2Ipc>	involves: 129S2/SvPas * C57BL/6	N	12138202
MGI:3608130	M	MP:0002631	abnormal epididymis morphology	Ncoa2<tm1.2Ipc>/Ncoa2<tm1.2Ipc>	involves: 129S2/SvPas * C57BL/6	N	12138202
MGI:3608130	M	MP:0005578	teratozoospermia	Ncoa2<tm1.2Ipc>/Ncoa2<tm1.2Ipc>	involves: 129S2/SvPas * C57BL/6	N	12138202
MGI:3608130	M	MP:0006380	abnormal spermatid morphology	Ncoa2<tm1.2Ipc>/Ncoa2<tm1.2Ipc>	involves: 129S2/SvPas * C57BL/6	N	12138202
MGI:3608130	M	MP:0006416	abnormal rete testis morphology	Ncoa2<tm1.2Ipc>/Ncoa2<tm1.2Ipc>	involves: 129S2/SvPas * C57BL/6	N	12138202
MGI:3608130	M	MP:0009231	detached acrosome	Ncoa2<tm1.2Ipc>/Ncoa2<tm1.2Ipc>	involves: 129S2/SvPas * C57BL/6	N	12138202
MGI:3608132	M	MP:0002784	abnormal Sertoli cell morphology	Abca1<tm1Wpfl>/Abca1<tm1Wpfl>	involves: 129 * C57BL/6	N	14993927
MGI:3608951	F	MP:0009326	absent maternal crouching	Oxtr<tm1.1Knis>/Oxtr<tm1.1Knis>	involves: 129P2/OlaHsd * C57BL/6J	N	16249339
MGI:3608951	M	MP:0001353	increased aggression towards mice	Oxtr<tm1.1Knis>/Oxtr<tm1.1Knis>	involves: 129P2/OlaHsd * C57BL/6J	N	16249339
MGI:3608951	M	MP:0031391	increased locomotor activity	Oxtr<tm1.1Knis>/Oxtr<tm1.1Knis>	involves: 129P2/OlaHsd * C57BL/6J	N	16249339
MGI:3608951	F	MP:0010249	lactation failure	Oxtr<tm1.1Knis>/Oxtr<tm1.1Knis>	involves: 129P2/OlaHsd * C57BL/6J	N	16249339
MGI:3608951	F	MP:0001384	abnormal pup retrieval	Oxtr<tm1.1Knis>/Oxtr<tm1.1Knis>	involves: 129P2/OlaHsd * C57BL/6J	N	16249339
MGI:3608951	F	MP:0001386	abnormal maternal nurturing	Oxtr<tm1.1Knis>/Oxtr<tm1.1Knis>	involves: 129P2/OlaHsd * C57BL/6J	N	16249339
MGI:3608951	M	MP:0001360	abnormal social investigation	Oxtr<tm1.1Knis>/Oxtr<tm1.1Knis>	involves: 129P2/OlaHsd * C57BL/6J	N	16249339
MGI:3608951	M	MP:0020351	decreased vocalization	Oxtr<tm1.1Knis>/Oxtr<tm1.1Knis>	involves: 129P2/OlaHsd * C57BL/6J	N	16249339
MGI:3608977	F	MP:0003537	hydrometrocolpos	Bbs4<Gt1Nk>/Bbs4<Gt1Nk>	involves: 129S7/SvEvBrd	N	16794820
MGI:3608977	F	MP:0002968	increased circulating alkaline phosphatase level	Bbs4<Gt1Nk>/Bbs4<Gt1Nk>	involves: 129S7/SvEvBrd	N	16794820
MGI:3608981	F	MP:0002865	increased growth rate	Mohg2<C57BL/6J>/Mohg2<CAST/EiJ>,Socs2<hg>/Socs2<hg>	involves: C57BL/6J * CAST/EiJ	N	15965258
MGI:3608983	F	MP:0002865	increased growth rate	Mohg3<C57BL/6J>/Mohg3<C57BL/6J>,Socs2<hg>/Socs2<hg>	involves: C57BL/6J * CAST/EiJ	N	15965258
MGI:3608984	F	MP:0002865	increased growth rate	Mohg2<C57BL/6J>/Mohg2<CAST/EiJ>	involves: C57BL/6J * CAST/EiJ	N	15965258
MGI:3608985	F	MP:0002865	increased growth rate	Mohg3<C57BL/6J>/Mohg3<CAST/EiJ>,Socs2<hg>/Socs2<hg>	involves: C57BL/6J * CAST/EiJ	N	15965258
MGI:3608987	M	MP:0006380	abnormal spermatid morphology	Clip1<tm1.1Gal>/Clip1<tm1.1Gal>	involves: 129P2/OlaHsd * C57BL/6	N	16230537
MGI:3608987	M	MP:0009376	abnormal manchette morphology	Clip1<tm1.1Gal>/Clip1<tm1.1Gal>	involves: 129P2/OlaHsd * C57BL/6	N	16230537
MGI:3608988	M	MP:0006380	abnormal spermatid morphology	Clip1<tm1Gal>/Clip1<tm1Gal>	involves: 129P2/OlaHsd * C57BL/6	N	16230537
MGI:3608988	M	MP:0008892	abnormal sperm flagellum morphology	Clip1<tm1Gal>/Clip1<tm1Gal>	involves: 129P2/OlaHsd * C57BL/6	N	16230537
MGI:3608988	M	MP:0009377	ectopic manchette	Clip1<tm1Gal>/Clip1<tm1Gal>	involves: 129P2/OlaHsd * C57BL/6	N	16230537
MGI:3608988	M	MP:0005578	teratozoospermia	Clip1<tm1Gal>/Clip1<tm1Gal>	involves: 129P2/OlaHsd * C57BL/6	N	16230537
MGI:3608988	M	MP:0001922	reduced male fertility	Clip1<tm1Gal>/Clip1<tm1Gal>	involves: 129P2/OlaHsd * C57BL/6	N	16230537
MGI:3608988	M	MP:0009376	abnormal manchette morphology	Clip1<tm1Gal>/Clip1<tm1Gal>	involves: 129P2/OlaHsd * C57BL/6	N	16230537
MGI:3608988	M	MP:0009230	abnormal sperm head morphology	Clip1<tm1Gal>/Clip1<tm1Gal>	involves: 129P2/OlaHsd * C57BL/6	N	16230537
MGI:3609189	M	MP:0001925	male infertility	Del(1)1Brk/Del(1)1Brk	CBA/J-Del(1)1Brk	N	15994289
MGI:3609191	M	MP:0001925	male infertility	Del(1)1Brk/Del(1)1Brk	B6.CBA-Del(1)1Brk	N	15994289
MGI:3609192	M	MP:0001932	abnormal spermiogenesis	Del(1)1Brk/Del(1)1Brk	involves: 129S6/SvEvTac * C57BL/6J * CBA/J	N	18039845
MGI:3609192	M	MP:0001925	male infertility	Del(1)1Brk/Del(1)1Brk	involves: 129S6/SvEvTac * C57BL/6J * CBA/J	N	18039845
MGI:3609192	M	MP:0005159	azoospermia	Del(1)1Brk/Del(1)1Brk	involves: 129S6/SvEvTac * C57BL/6J * CBA/J	N	18039845
MGI:3609192	M	MP:0001925	male infertility	Del(1)1Brk/Del(1)1Brk	involves: 129S6/SvEvTac * C57BL/6J * CBA/J	N	15994289
MGI:3609192	M	MP:0001940	testis hypoplasia	Del(1)1Brk/Del(1)1Brk	involves: 129S6/SvEvTac * C57BL/6J * CBA/J	N	15994289
MGI:3609192	M	MP:0008545	absent sperm flagellum	Del(1)1Brk/Del(1)1Brk	involves: 129S6/SvEvTac * C57BL/6J * CBA/J	N	18039845
MGI:3609494	M	MP:0001925	male infertility	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	11711676
MGI:3609494	M	MP:0009839	multiflagellated sperm	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	15705627
MGI:3609494	M	MP:0009232	abnormal sperm nucleus morphology	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	14724135
MGI:3609494	M	MP:0009233	enlarged sperm head	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	15705627
MGI:3609494	M	MP:0009232	abnormal sperm nucleus morphology	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	11711676
MGI:3609494	M	MP:0009838	abnormal sperm axoneme morphology	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	14724135
MGI:3609494	M	MP:0008898	abnormal acrosome morphology	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	14724135
MGI:3609494	M	MP:0005578	teratozoospermia	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	11711676
MGI:3609494	M	MP:0008279	arrest of spermiogenesis	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	11711676
MGI:3609494	M	MP:0005578	teratozoospermia	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	15705627
MGI:3609494	M	MP:0009833	absent sperm mitochondrial sheath	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	11711676
MGI:3609494	M	MP:0031386	elongated manchette	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	14724135
MGI:3609494	M	MP:0008839	absent acrosome	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	11711676
MGI:3609494	M	MP:0009232	abnormal sperm nucleus morphology	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	15705627
MGI:3609494	M	MP:0009376	abnormal manchette morphology	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	14724135
MGI:3609494	M	MP:0009377	ectopic manchette	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	14724135
MGI:3609494	M	MP:0002675	asthenozoospermia	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	15705627
MGI:3609494	M	MP:0002675	asthenozoospermia	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	11711676
MGI:3609494	M	MP:0002686	globozoospermia	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	11711676
MGI:3609494	M	MP:0031355	abnormal proacrosomal vesicle fusion	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	11711676
MGI:3609494	M	MP:0009830	abnormal sperm connecting piece morphology	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	14724135
MGI:3609494	M	MP:0002687	oligozoospermia	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	11711676
MGI:3609494	M	MP:0030980	abnormal acroplaxome morphology	Agfg1<tm1Jvd>/Agfg1<tm1Jvd>	involves: 129P2/OlaHsd	N	14724135
MGI:3609961	F	MP:0002169	no abnormal phenotype detected	Gpr82<tm1Lex>/Gpr82<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:3609573
MGI:3609965	M	MP:0013600	testis degeneration	Ip6k1<Gt(OST137568)Lex>/Ip6k1<Gt(OST137568)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:3609573
MGI:3609965	M	MP:0005159	azoospermia	Ip6k1<Gt(OST137568)Lex>/Ip6k1<Gt(OST137568)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:3609573
MGI:3609973	F	MP:0002169	no abnormal phenotype detected	Hs6st2<tm1Lex>/Hs6st2<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:3609573
MGI:3609974	M	MP:0002169	no abnormal phenotype detected	Hs6st2<tm1Lex>/Y	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:3609573
MGI:3610026	M	MP:0001925	male infertility	Plin2<Gt(OST170322)Lex>/Plin2<Gt(OST170322)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:3609573
MGI:3610379	F	MP:0001882	abnormal lactation	Csf1<op>/Csf1<op>	B6C3Fe a/a-Csf1<op>/J	N	7937762
MGI:3610379	M	MP:0001922	reduced male fertility	Csf1<op>/Csf1<op>	B6C3Fe a/a-Csf1<op>/J	N	8828834
MGI:3610379	F	MP:0009506	abnormal mammary gland alveolus morphology	Csf1<op>/Csf1<op>	B6C3Fe a/a-Csf1<op>/J	N	7937762
MGI:3610379	M	MP:0004851	increased testis weight	Csf1<op>/Csf1<op>	B6C3Fe a/a-Csf1<op>/J	N	8828834
MGI:3610379	M	MP:0002687	oligozoospermia	Csf1<op>/Csf1<op>	B6C3Fe a/a-Csf1<op>/J	N	8828834
MGI:3610379	F	MP:0031336	abnormal uterine epithelium development	Csf1<op>/Csf1<op>	B6C3Fe a/a-Csf1<op>/J	N	1887865
MGI:3610379	M	MP:0009325	necrospermia	Csf1<op>/Csf1<op>	B6C3Fe a/a-Csf1<op>/J	N	8828834
MGI:3610379	F	MP:0000662	abnormal branching of the mammary ductal tree	Csf1<op>/Csf1<op>	B6C3Fe a/a-Csf1<op>/J	N	7937762
MGI:3610379	F	MP:0009091	endometrium hypoplasia	Csf1<op>/Csf1<op>	B6C3Fe a/a-Csf1<op>/J	N	1887865
MGI:3610379	F	MP:0006269	abnormal mammary gland growth during pregnancy	Csf1<op>/Csf1<op>	B6C3Fe a/a-Csf1<op>/J	N	7937762
MGI:3610379	F	MP:0000628	abnormal mammary gland development	Csf1<op>/Csf1<op>	B6C3Fe a/a-Csf1<op>/J	N	7937762
MGI:3610379	F	MP:0009090	myometrium hypoplasia	Csf1<op>/Csf1<op>	B6C3Fe a/a-Csf1<op>/J	N	1887865
MGI:3610499	F	MP:0009013	abnormal proestrus	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	9002639
MGI:3610499	F	MP:0000628	abnormal mammary gland development	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	7937762
MGI:3610499	F	MP:0000662	abnormal branching of the mammary ductal tree	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	7937762
MGI:3610499	F	MP:0009505	abnormal mammary gland lobule morphology	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	7937762
MGI:3610499	M	MP:0002673	abnormal sperm number	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	8828834
MGI:3610499	F	MP:0006270	abnormal mammary gland growth during lactation	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	7937762
MGI:3610499	M	MP:0004884	abnormal testis physiology	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	8828834
MGI:3610499	F	MP:0003355	decreased ovulation rate	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	9002639
MGI:3610499	F	MP:0001126	abnormal ovary morphology	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	9002639
MGI:3610499	F	MP:0001923	reduced female fertility	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	9002639
MGI:3610499	M	MP:0001380	reduced male mating frequency	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	8828834
MGI:3610499	F	MP:0009006	prolonged estrous cycle	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	9002639
MGI:3610499	F	MP:0001729	impaired embryo implantation	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	9002639
MGI:3610499	F	MP:0001928	abnormal ovulation	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	9002639
MGI:3610499	F	MP:0001882	abnormal lactation	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	7937762
MGI:3610499	F	MP:0002680	decreased corpora lutea number	Csf1<op>/Csf1<op>	involves: C3HeB/FeJ * C57BL/6J	N	9002639
MGI:3610502	F	MP:0002135	abnormal kidney morphology	Col4a5<tm1Yseg>/Col4a5<+>	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610502	F	MP:0002703	abnormal renal tubule morphology	Col4a5<tm1Yseg>/Col4a5<+>	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610502	F	MP:0004969	pale kidney	Col4a5<tm1Yseg>/Col4a5<+>	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610502	F	MP:0005253	abnormal eye physiology	Col4a5<tm1Yseg>/Col4a5<+>	B6.Cg-Col4a5<tm1Yseg>	N	23707242
MGI:3610502	F	MP:0002083	premature death	Col4a5<tm1Yseg>/Col4a5<+>	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610502	F	MP:0005565	increased blood urea nitrogen level	Col4a5<tm1Yseg>/Col4a5<+>	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610502	F	MP:0003236	abnormal lens capsule morphology	Col4a5<tm1Yseg>/Col4a5<+>	B6.Cg-Col4a5<tm1Yseg>	N	23707242
MGI:3610502	F	MP:0005325	abnormal renal glomerulus morphology	Col4a5<tm1Yseg>/Col4a5<+>	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610502	F	MP:0002962	increased urine protein level	Col4a5<tm1Yseg>/Col4a5<+>	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0002135	abnormal kidney morphology	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0008140	podocyte foot process effacement	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0005565	increased blood urea nitrogen level	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0005325	abnormal renal glomerulus morphology	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0005253	abnormal eye physiology	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	23707242
MGI:3610503	M	MP:0011348	abnormal renal glomerulus basement membrane morphology	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0011405	tubulointerstitial nephritis	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0011346	renal tubule atrophy	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0011320	abnormal glomerular capillary morphology	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0002705	dilated renal tubule	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0005264	glomerulosclerosis	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0011427	increased mesangial cell number	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0002083	premature death	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0011483	renal glomerular synechia	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0011509	dilated glomerular capillary	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0002962	increased urine protein level	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3610503	M	MP:0003236	abnormal lens capsule morphology	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	23707242
MGI:3610503	M	MP:0004969	pale kidney	Col4a5<tm1Yseg>/Y	B6.Cg-Col4a5<tm1Yseg>	N	15153557
MGI:3611357	F	MP:0002026	increased leukemia incidence	Rv3<C57BL/6J>/Rv3<C57BL/6J>	involves: C57BL/6J * CBA/Lac	N	6489477
MGI:3611358	F	MP:0002026	increased leukemia incidence	Rv3<C57BL/6J>/Rv3<CBA/Lac>	involves: C57BL/6J * CBA/Lac	N	6489477
MGI:3611359	F	MP:0002026	increased leukemia incidence	Rv3<CBA/Lac>/Rv3<CBA/Lac>	involves: C57BL/6J * CBA/Lac	N	6489477
MGI:3611443	M	MP:0001147	small testis	Wt1<tm2Hst>/Wt1<+>	chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac	N	16245160
MGI:3611443	M	MP:0001925	male infertility	Wt1<tm2Hst>/Wt1<+>	chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac	N	10077614
MGI:3611443	M	MP:0005159	azoospermia	Wt1<tm2Hst>/Wt1<+>	chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac	N	16245160
MGI:3611443	M	MP:0001147	small testis	Wt1<tm2Hst>/Wt1<+>	chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac	N	10077614
MGI:3611491	M	MP:0002169	no abnormal phenotype detected	Septin6<tm1Nosa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	16314519
MGI:3611492	F	MP:0002169	no abnormal phenotype detected	Septin6<tm1Nosa>/Septin6<tm1Nosa>	involves: 129P2/OlaHsd * C57BL/6	N	16314519
MGI:3611494	F	MP:0001881	abnormal mammary gland physiology	Hoxc6<tm1Dds>/Hoxc6<tm1Dds>	involves: 129S7/SvEvBrd * C57BL/6	N	11002345
MGI:3611494	F	MP:0001882	abnormal lactation	Hoxc6<tm1Dds>/Hoxc6<tm1Dds>	involves: 129S7/SvEvBrd * C57BL/6	N	11002345
MGI:3611755	M	MP:0012029	abnormal electroretinogram waveform feature	Cacna1f<tm1Ntbh>/Y	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611755	M	MP:0005551	abnormal eye electrophysiology	Cacna1f<tm1Ntbh>/Y	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611755	M	MP:0006074	abnormal retina rod bipolar cell morphology	Cacna1f<tm1Ntbh>/Y	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611755	M	MP:0010749	absent visual evoked potential	Cacna1f<tm1Ntbh>/Y	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611755	M	MP:0006068	abnormal retina horizontal cell morphology	Cacna1f<tm1Ntbh>/Y	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611755	M	MP:0006069	abnormal retina neuronal layer morphology	Cacna1f<tm1Ntbh>/Y	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611755	M	MP:0000968	abnormal sensory neuron innervation pattern	Cacna1f<tm1Ntbh>/Y	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611755	M	MP:0008519	thin retina outer plexiform layer	Cacna1f<tm1Ntbh>/Y	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611756	F	MP:0008519	thin retina outer plexiform layer	Cacna1f<tm1Ntbh>/Cacna1f<tm1Ntbh>	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611756	F	MP:0005551	abnormal eye electrophysiology	Cacna1f<tm1Ntbh>/Cacna1f<tm1Ntbh>	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611756	F	MP:0012029	abnormal electroretinogram waveform feature	Cacna1f<tm1Ntbh>/Cacna1f<tm1Ntbh>	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611756	F	MP:0000968	abnormal sensory neuron innervation pattern	Cacna1f<tm1Ntbh>/Cacna1f<tm1Ntbh>	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611756	F	MP:0006069	abnormal retina neuronal layer morphology	Cacna1f<tm1Ntbh>/Cacna1f<tm1Ntbh>	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611756	F	MP:0006074	abnormal retina rod bipolar cell morphology	Cacna1f<tm1Ntbh>/Cacna1f<tm1Ntbh>	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611756	F	MP:0006068	abnormal retina horizontal cell morphology	Cacna1f<tm1Ntbh>/Cacna1f<tm1Ntbh>	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611756	F	MP:0010749	absent visual evoked potential	Cacna1f<tm1Ntbh>/Cacna1f<tm1Ntbh>	B6.129-Cacna1f<tm1Ntbh>	N	16155113
MGI:3611807	M	MP:0001559	hyperglycemia	Alms1<bbb>/Alms1<bbb>	C57BL/6JSfdAnu-Alms1<bbb>/Anu	N	MGI:3611487
MGI:3612159	F	MP:0003058	increased insulin secretion	Sytl4<tm1Tiz>/Sytl4<tm1Tiz>	involves: 129P2/OlaHsd * C3H/He	N	16216924
MGI:3612159	F	MP:0001262	decreased body weight	Sytl4<tm1Tiz>/Sytl4<tm1Tiz>	involves: 129P2/OlaHsd * C3H/He	N	16216924
MGI:3612159	F	MP:0005560	decreased circulating glucose level	Sytl4<tm1Tiz>/Sytl4<tm1Tiz>	involves: 129P2/OlaHsd * C3H/He	N	16216924
MGI:3612159	F	MP:0005217	abnormal pancreatic beta cell morphology	Sytl4<tm1Tiz>/Sytl4<tm1Tiz>	involves: 129P2/OlaHsd * C3H/He	N	16216924
MGI:3612260	M	MP:0001925	male infertility	Oca2<p-103G>/Oca2<p-103G>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3612385	F	MP:0001927	abnormal estrous cycle	Hoxa5<tm1Rob>/Hoxa5<tm1Rob>	129S(Cg)-Hoxa5<tm1Rob>	N	22315454
MGI:3612385	F	MP:0009020	prolonged metestrus	Hoxa5<tm1Rob>/Hoxa5<tm1Rob>	129S(Cg)-Hoxa5<tm1Rob>	N	22315454
MGI:3612385	F	MP:0009018	short estrus	Hoxa5<tm1Rob>/Hoxa5<tm1Rob>	129S(Cg)-Hoxa5<tm1Rob>	N	22315454
MGI:3612385	F	MP:0009011	prolonged diestrus	Hoxa5<tm1Rob>/Hoxa5<tm1Rob>	129S(Cg)-Hoxa5<tm1Rob>	N	22315454
MGI:3612385	F	MP:0002016	ovary cyst	Hoxa5<tm1Rob>/Hoxa5<tm1Rob>	129S(Cg)-Hoxa5<tm1Rob>	N	22315454
MGI:3612385	F	MP:0009006	prolonged estrous cycle	Hoxa5<tm1Rob>/Hoxa5<tm1Rob>	129S(Cg)-Hoxa5<tm1Rob>	N	22315454
MGI:3612385	F	MP:0005182	increased circulating estradiol level	Hoxa5<tm1Rob>/Hoxa5<tm1Rob>	129S(Cg)-Hoxa5<tm1Rob>	N	22315454
MGI:3612385	F	MP:0003378	early sexual maturation	Hoxa5<tm1Rob>/Hoxa5<tm1Rob>	129S(Cg)-Hoxa5<tm1Rob>	N	22315454
MGI:3612446	M	MP:0001380	reduced male mating frequency	Gria2<tm3Rsp>/Gria2<tm3Rsp>,Tg(Gnrh1-cre)1Rsp/0	involves: C57BL/6	N	16099814
MGI:3612446	F	MP:0001384	abnormal pup retrieval	Gria2<tm3Rsp>/Gria2<tm3Rsp>,Tg(Gnrh1-cre)1Rsp/0	involves: C57BL/6	N	16099814
MGI:3612446	M	MP:0002566	abnormal sexual interaction	Gria2<tm3Rsp>/Gria2<tm3Rsp>,Tg(Gnrh1-cre)1Rsp/0	involves: C57BL/6	N	16099814
MGI:3612446	M	MP:0031629	abnormal mounting behavior	Gria2<tm3Rsp>/Gria2<tm3Rsp>,Tg(Gnrh1-cre)1Rsp/0	involves: C57BL/6	N	16099814
MGI:3612869	M	MP:0002216	abnormal seminiferous tubule morphology	Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>,Bik<tm1Ast>/Bik<tm1Ast>	B6.Cg-Bcl2l11<tm1.1Ast> Bik<tm1Ast>	N	16270031
MGI:3612869	M	MP:0020550	multinucleated giant male germ cells	Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>,Bik<tm1Ast>/Bik<tm1Ast>	B6.Cg-Bcl2l11<tm1.1Ast> Bik<tm1Ast>	N	16270031
MGI:3612869	M	MP:0005159	azoospermia	Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>,Bik<tm1Ast>/Bik<tm1Ast>	B6.Cg-Bcl2l11<tm1.1Ast> Bik<tm1Ast>	N	16270031
MGI:3612869	M	MP:0001156	abnormal spermatogenesis	Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>,Bik<tm1Ast>/Bik<tm1Ast>	B6.Cg-Bcl2l11<tm1.1Ast> Bik<tm1Ast>	N	16270031
MGI:3612869	M	MP:0004852	decreased testis weight	Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>,Bik<tm1Ast>/Bik<tm1Ast>	B6.Cg-Bcl2l11<tm1.1Ast> Bik<tm1Ast>	N	16270031
MGI:3612869	M	MP:0001925	male infertility	Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>,Bik<tm1Ast>/Bik<tm1Ast>	B6.Cg-Bcl2l11<tm1.1Ast> Bik<tm1Ast>	N	16270031
MGI:3612869	M	MP:0008261	arrest of male meiosis	Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>,Bik<tm1Ast>/Bik<tm1Ast>	B6.Cg-Bcl2l11<tm1.1Ast> Bik<tm1Ast>	N	16270031
MGI:3612870	M	MP:0004852	decreased testis weight	Bax<tm1Sjk>/Bax<tm1Sjk>	B6.129X1-Bax<tm1Sjk>/J	N	16270031
MGI:3612870	M	MP:0001925	male infertility	Bax<tm1Sjk>/Bax<tm1Sjk>	B6.129X1-Bax<tm1Sjk>/J	N	16270031
MGI:3612870	M	MP:0008261	arrest of male meiosis	Bax<tm1Sjk>/Bax<tm1Sjk>	B6.129X1-Bax<tm1Sjk>/J	N	16270031
MGI:3612870	M	MP:0005159	azoospermia	Bax<tm1Sjk>/Bax<tm1Sjk>	B6.129X1-Bax<tm1Sjk>/J	N	16270031
MGI:3612870	M	MP:0002216	abnormal seminiferous tubule morphology	Bax<tm1Sjk>/Bax<tm1Sjk>	B6.129X1-Bax<tm1Sjk>/J	N	16270031
MGI:3612870	M	MP:0001156	abnormal spermatogenesis	Bax<tm1Sjk>/Bax<tm1Sjk>	B6.129X1-Bax<tm1Sjk>/J	N	16270031
MGI:3612872	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>	B6.129-Bcl2l11<tm1.1Ast> Bax<tm1Sjk>	N	16270031
MGI:3612872	M	MP:0008261	arrest of male meiosis	Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>	B6.129-Bcl2l11<tm1.1Ast> Bax<tm1Sjk>	N	16270031
MGI:3612872	M	MP:0001153	small seminiferous tubules	Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>	B6.129-Bcl2l11<tm1.1Ast> Bax<tm1Sjk>	N	16270031
MGI:3612872	M	MP:0005159	azoospermia	Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>	B6.129-Bcl2l11<tm1.1Ast> Bax<tm1Sjk>	N	16270031
MGI:3612872	M	MP:0001925	male infertility	Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>	B6.129-Bcl2l11<tm1.1Ast> Bax<tm1Sjk>	N	16270031
MGI:3612961	F	MP:0003995	abnormal uterine artery morphology	Klk1<tm1Pmtn>/Klk1<tm1Pmtn>	involves: 129/Sv * C57BL/6	N	12933530
MGI:3612993	F	MP:0001923	reduced female fertility	Gabbr1<tm1Bet>/Gabbr1<tm1Bet>	BALB/c-Gabbr1<tm1Bet>	N	16682806
MGI:3612993	F	MP:0009015	short proestrus	Gabbr1<tm1Bet>/Gabbr1<tm1Bet>	BALB/c-Gabbr1<tm1Bet>	N	16682806
MGI:3612993	F	MP:0001927	abnormal estrous cycle	Gabbr1<tm1Bet>/Gabbr1<tm1Bet>	BALB/c-Gabbr1<tm1Bet>	N	16682806
MGI:3612993	F	MP:0009017	prolonged estrus	Gabbr1<tm1Bet>/Gabbr1<tm1Bet>	BALB/c-Gabbr1<tm1Bet>	N	16682806
MGI:3613012	F	MP:0003699	abnormal female reproductive system physiology	Ncoa3<tm1Jxu>/Ncoa3<tm1Jxu>	involves: 129S6/SvEvTac	N	10823921
MGI:3613012	F	MP:0009006	prolonged estrous cycle	Ncoa3<tm1Jxu>/Ncoa3<tm1Jxu>	involves: 129S6/SvEvTac	N	10823921
MGI:3613012	F	MP:0002636	delayed vaginal opening	Ncoa3<tm1Jxu>/Ncoa3<tm1Jxu>	involves: 129S6/SvEvTac	N	10823921
MGI:3613012	F	MP:0000628	abnormal mammary gland development	Ncoa3<tm1Jxu>/Ncoa3<tm1Jxu>	involves: 129S6/SvEvTac	N	10823921
MGI:3613012	F	MP:0001140	abnormal vagina epithelium morphology	Ncoa3<tm1Jxu>/Ncoa3<tm1Jxu>	involves: 129S6/SvEvTac	N	10823921
MGI:3613012	F	MP:0031420	decreased superovulation rate	Ncoa3<tm1Jxu>/Ncoa3<tm1Jxu>	involves: 129S6/SvEvTac	N	10823921
MGI:3613012	F	MP:0005181	decreased circulating estradiol level	Ncoa3<tm1Jxu>/Ncoa3<tm1Jxu>	involves: 129S6/SvEvTac	N	10823921
MGI:3613012	F	MP:0001938	delayed sexual maturation	Ncoa3<tm1Jxu>/Ncoa3<tm1Jxu>	involves: 129S6/SvEvTac	N	10823921
MGI:3613012	F	MP:0000662	abnormal branching of the mammary ductal tree	Ncoa3<tm1Jxu>/Ncoa3<tm1Jxu>	involves: 129S6/SvEvTac	N	10823921
MGI:3613075	M	MP:0001925	male infertility	Agtpbp1<atms>/Agtpbp1<atms>,Fas<lpr>/?	MRL/Mp-Agtpbp1<atms> Fas<lpr>	N	12787313
MGI:3613075	F	MP:0001926	female infertility	Agtpbp1<atms>/Agtpbp1<atms>,Fas<lpr>/?	MRL/Mp-Agtpbp1<atms> Fas<lpr>	N	12787313
MGI:3613075	M	MP:0002687	oligozoospermia	Agtpbp1<atms>/Agtpbp1<atms>,Fas<lpr>/?	MRL/Mp-Agtpbp1<atms> Fas<lpr>	N	12787313
MGI:3613075	M	MP:0001155	arrest of spermatogenesis	Agtpbp1<atms>/Agtpbp1<atms>,Fas<lpr>/?	MRL/Mp-Agtpbp1<atms> Fas<lpr>	N	12787313
MGI:3613373	M	MP:0020560	abnormal pontine nuclei morphology	Tor1a<tm1Yql>/Tor1a<+>	involves: 129S2/SvPas * C57BL/6	N	16242683
MGI:3613373	M	MP:0005643	decreased dopamine level	Tor1a<tm1Yql>/Tor1a<+>	involves: 129S2/SvPas * C57BL/6	N	16242683
MGI:3613373	M	MP:0001525	impaired balance	Tor1a<tm1Yql>/Tor1a<+>	involves: 129S2/SvPas * C57BL/6	N	16242683
MGI:3613373	M	MP:0031391	increased locomotor activity	Tor1a<tm1Yql>/Tor1a<+>	involves: 129S2/SvPas * C57BL/6	N	16242683
MGI:3613444	M	MP:0002169	no abnormal phenotype detected	Zbtb33<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	16354691
MGI:3613445	F	MP:0002169	no abnormal phenotype detected	Zbtb33<tm1.1Bird>/Zbtb33<tm1.1Bird>	involves: 129P2/OlaHsd * C57BL/6	N	16354691
MGI:3613447	M	MP:0002404	increased intestinal adenoma incidence	Apc<Min>/Apc<+>,Zbtb33<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	N	16354691
MGI:3613447	M	MP:0003447	decreased tumor growth/size	Apc<Min>/Apc<+>,Zbtb33<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	N	16354691
MGI:3613447	M	MP:0002083	premature death	Apc<Min>/Apc<+>,Zbtb33<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	N	16354691
MGI:3613464	M	MP:0001148	enlarged testis	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: 129/Sv * C57BL/6 * CD-1	N	15647389
MGI:3613464	M	MP:0001156	abnormal spermatogenesis	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: 129/Sv * C57BL/6 * CD-1	N	15647389
MGI:3613464	M	MP:0005389	reproductive system phenotype	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: 129/Sv * C57BL/6 * CD-1	Y	15647389
MGI:3613464	M	MP:0004851	increased testis weight	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: 129/Sv * C57BL/6 * CD-1	N	15647389
MGI:3613571	M	MP:0002997	enlarged seminal vesicle	Atxn2<tm1Plt>/Atxn2<tm1Plt>	involves: 129X1/SvJ * C57BL/6	N	16293225
MGI:3613583	F	MP:0004819	decreased skeletal muscle mass	Srpk3<tm1Eno>/Srpk3<tm1Eno>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6J)	N	16140986
MGI:3613583	F	MP:0009404	centrally nucleated skeletal muscle fibers	Srpk3<tm1Eno>/Srpk3<tm1Eno>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6J)	N	16140986
MGI:3613583	F	MP:0000759	abnormal skeletal muscle morphology	Srpk3<tm1Eno>/Srpk3<tm1Eno>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6J)	N	16140986
MGI:3613589	M	MP:0000759	abnormal skeletal muscle morphology	Srpk3<tm1Eno>/Y	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6J)	N	16140986
MGI:3613589	M	MP:0009404	centrally nucleated skeletal muscle fibers	Srpk3<tm1Eno>/Y	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6J)	N	16140986
MGI:3613589	M	MP:0004819	decreased skeletal muscle mass	Srpk3<tm1Eno>/Y	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6J)	N	16140986
MGI:3613607	F	MP:0001382	abnormal nursing	snthr2/snthr2	involves: DBA/2	N	15541636
MGI:3613609	F	MP:0001382	abnormal nursing	snthr/snthr	involves: DBA/2	N	15541636
MGI:3613762	M	MP:0004618	thoracic vertebral transformation	Cdx4<tm1.1Jdes>/Y	involves: 129P2/OlaHsd * C57BL/6 * CBA * FVB	N	16396910
MGI:3613764	M	MP:0003345	decreased rib number	Cdx1<tm1Pgr>/Cdx1<tm1Pgr>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613764	M	MP:0004618	thoracic vertebral transformation	Cdx1<tm1Pgr>/Cdx1<tm1Pgr>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613767	M	MP:0003036	vertebral transformation	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613767	M	MP:0004616	lumbar vertebral transformation	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613767	M	MP:0001785	edema	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613767	M	MP:0009657	failure of chorioallantoic fusion	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613767	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613767	M	MP:0003984	embryonic growth retardation	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613767	M	MP:0004618	thoracic vertebral transformation	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613767	M	MP:0001726	abnormal allantois morphology	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613767	M	MP:0001711	abnormal placenta morphology	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613767	M	MP:0003231	abnormal placenta vasculature	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613767	M	MP:0000480	increased rib number	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613767	M	MP:0001716	abnormal placenta labyrinth morphology	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613767	M	MP:0003445	sirenomelia	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Y	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613771	F	MP:0001716	abnormal placenta labyrinth morphology	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Cdx4<+>	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3613771	F	MP:0009657	failure of chorioallantoic fusion	Cdx2<tm1Fbe>/Cdx2<+>,Cdx4<tm1.1Jdes>/Cdx4<+>	involves: 129 * C57BL/6 * CBA * FVB	N	16396910
MGI:3614284	F	MP:0011967	increased or absent threshold for auditory brainstem response	tmgc59/tmgc59	C57BL/6-19<PWK>	N	MGI:3053008
MGI:3614341	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(MMTV-PyVT*Y250F)250-2Mul/?	FVB/N-Tg(MMTV-PyVT*Y250F)250-2Mul	N	9528804
MGI:3614342	F	MP:0014126	increased mammary gland apoptosis	Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul/?	FVB/N-Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul	N	9528804
MGI:3614342	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul/?	FVB/N-Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul	N	9528804
MGI:3614342	F	MP:0000630	mammary gland hyperplasia	Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul/?	FVB/N-Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul	N	9528804
MGI:3614388	F	MP:0004008	abnormal GABA-mediated receptor currents	Gabra3<tm2Uru>/Gabra3<tm2Uru>	129X1(Cg)-Gabra3<tm2Uru>	N	16284244
MGI:3614388	F	MP:0009142	decreased prepulse inhibition	Gabra3<tm2Uru>/Gabra3<tm2Uru>	129X1(Cg)-Gabra3<tm2Uru>	N	16284244
MGI:3614388	F	MP:0031391	increased locomotor activity	Gabra3<tm2Uru>/Gabra3<tm2Uru>	129X1(Cg)-Gabra3<tm2Uru>	N	16284244
MGI:3614389	F	MP:0005376	homeostasis/metabolism phenotype	Gabra3<tm1.1Uru>/Gabra3<tm1.1Uru>	129-Gabra3<tm1.1Uru>	Y	11021797
MGI:3614391	M	MP:0001925	male infertility	Arhgdia<tm1Ytk>/Arhgdia<tm1Ytk>	involves: 129S/SvEv * C57BL/6 * DBA	N	10498891
MGI:3614391	M	MP:0002687	oligozoospermia	Arhgdia<tm1Ytk>/Arhgdia<tm1Ytk>	involves: 129S/SvEv * C57BL/6 * DBA	N	10498891
MGI:3614391	F	MP:0001923	reduced female fertility	Arhgdia<tm1Ytk>/Arhgdia<tm1Ytk>	involves: 129S/SvEv * C57BL/6 * DBA	N	10498891
MGI:3614391	M	MP:0002216	abnormal seminiferous tubule morphology	Arhgdia<tm1Ytk>/Arhgdia<tm1Ytk>	involves: 129S/SvEv * C57BL/6 * DBA	N	10498891
MGI:3614391	F	MP:0004014	abnormal uterine environment	Arhgdia<tm1Ytk>/Arhgdia<tm1Ytk>	involves: 129S/SvEv * C57BL/6 * DBA	N	10498891
MGI:3614391	F	MP:0031420	decreased superovulation rate	Arhgdia<tm1Ytk>/Arhgdia<tm1Ytk>	involves: 129S/SvEv * C57BL/6 * DBA	N	10498891
MGI:3614392	M	MP:0004008	abnormal GABA-mediated receptor currents	Gabra3<tm2Uru>/Y	129X1(Cg)-Gabra3<tm2Uru>	N	16284244
MGI:3614392	M	MP:0009142	decreased prepulse inhibition	Gabra3<tm2Uru>/Y	129X1(Cg)-Gabra3<tm2Uru>	N	16284244
MGI:3614392	M	MP:0031391	increased locomotor activity	Gabra3<tm2Uru>/Y	129X1(Cg)-Gabra3<tm2Uru>	N	16284244
MGI:3614439	F	MP:0002637	small uterus	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	M	MP:0001925	male infertility	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	F	MP:0003344	mammary gland hypoplasia	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	M	MP:0001153	small seminiferous tubules	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	F	MP:0009226	small uterine cervix	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	M	MP:0001145	abnormal male reproductive system morphology	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	F	MP:0001119	abnormal female reproductive system morphology	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	M	MP:0004930	small epididymis	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	M	MP:0006401	absent male preputial gland	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	M	MP:0005536	decreased Leydig cell number	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	F	MP:0001926	female infertility	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	F	MP:0008983	small vagina	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	F	MP:0001121	uterus hypoplasia	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	M	MP:0005188	small penis	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	M	MP:0004852	decreased testis weight	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	M	MP:0001159	absent prostate gland	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	F	MP:0001127	small ovary	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614439	M	MP:0003642	absent seminal vesicle	Kiss1r<tm1Gstn>/Kiss1r<tm1Gstn>	involves: 129P2/OlaHsd	N	14652023
MGI:3614453	M	MP:0005553	increased circulating creatinine level	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0002083	premature death	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0001146	abnormal testis morphology	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16400023
MGI:3614453	M	MP:0000748	progressive muscle weakness	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0000747	muscle weakness	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0000751	myopathy	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0002784	abnormal Sertoli cell morphology	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16400023
MGI:3614453	M	MP:0009413	skeletal muscle fiber atrophy	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0003084	abnormal skeletal muscle fiber morphology	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0001922	reduced male fertility	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16400023
MGI:3614453	M	MP:0001156	abnormal spermatogenesis	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16400023
MGI:3614453	M	MP:0009404	centrally nucleated skeletal muscle fibers	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0003157	impaired muscle relaxation	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0000539	distended urinary bladder	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0001265	decreased body size	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0002216	abnormal seminiferous tubule morphology	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0010053	decreased grip strength	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0000938	motor neuron degeneration	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0001751	increased circulating luteinizing hormone level	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16400023
MGI:3614453	M	MP:0004145	abnormal muscle electrophysiology	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0000955	abnormal spinal cord morphology	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0003205	testicular atrophy	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16400023
MGI:3614453	M	MP:0002780	decreased circulating testosterone level	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0002687	oligozoospermia	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16400023
MGI:3614453	M	MP:0002790	decreased circulating follicle stimulating hormone level	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16400023
MGI:3614453	M	MP:0003205	testicular atrophy	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0005565	increased blood urea nitrogen level	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0009642	abnormal blood homeostasis	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0020378	abnormal cell cytoskeleton morphology	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16400023
MGI:3614453	M	MP:0004852	decreased testis weight	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16400023
MGI:3614453	M	MP:0005627	increased circulating potassium level	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0001922	reduced male fertility	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0009403	increased variability of skeletal muscle fiber size	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614453	M	MP:0011532	decreased urine major urinary protein level	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16400023
MGI:3614453	M	MP:0001262	decreased body weight	Ar<tm4(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3614473	M	MP:0005389	reproductive system phenotype	Ar<tm2(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	Y	16400023
MGI:3614831	M	MP:0004910	decreased seminal vesicle weight	Hom1<A/Ph>/Hom1<A/Ph>	involves: A/Ph * C57BL/10ScSnPh	N	4695943
MGI:3614831	M	MP:0004851	increased testis weight	Hom1<A/Ph>/Hom1<A/Ph>	involves: A/Ph * C57BL/10ScSnPh	N	4695943
MGI:3614834	M	MP:0004910	decreased seminal vesicle weight	Hom1<AKR>/Hom1<AKR>	involves: A/Ph * C57BL/10ScSnPh	N	4695943
MGI:3614834	M	MP:0004851	increased testis weight	Hom1<AKR>/Hom1<AKR>	involves: A/Ph * C57BL/10ScSnPh	N	4695943
MGI:3614946	M	MP:0002686	globozoospermia	Vps54<wr>/Vps54<wr>	multiple strains	N	1955109
MGI:3614946	M	MP:0004852	decreased testis weight	Vps54<wr>/Vps54<wr>	multiple strains	N	1955109
MGI:3614946	M	MP:0002675	asthenozoospermia	Vps54<wr>/Vps54<wr>	multiple strains	N	1955109
MGI:3614946	M	MP:0002687	oligozoospermia	Vps54<wr>/Vps54<wr>	multiple strains	N	1955109
MGI:3614956	F	MP:0009304	increased retroperitoneal fat pad weight	Obq22<NZB/BlNJ>/Obq22<NZB/BlNJ>	involves: NZB/BlNJ * SM/J	N	16416088
MGI:3614956	F	MP:0009285	increased gonadal fat pad weight	Obq22<NZB/BlNJ>/Obq22<NZB/BlNJ>	involves: NZB/BlNJ * SM/J	N	16416088
MGI:3614957	F	MP:0009285	increased gonadal fat pad weight	Obq22<NZB/BlNJ>/Obq22<SM/J>	involves: NZB/BlNJ * SM/J	N	16416088
MGI:3614957	F	MP:0009304	increased retroperitoneal fat pad weight	Obq22<NZB/BlNJ>/Obq22<SM/J>	involves: NZB/BlNJ * SM/J	N	16416088
MGI:3615049	F	MP:0001923	reduced female fertility	Spta1<ihj>/Spta1<ihj>	involves: HRS/J * LAH	N	MGI:3614961
MGI:3615049	F	MP:0001386	abnormal maternal nurturing	Spta1<ihj>/Spta1<ihj>	involves: HRS/J * LAH	N	MGI:3614961
MGI:3615252	F	MP:0000630	mammary gland hyperplasia	Ets2<tm3Rgo>/Ets2<tm3.1Rgo>,Meox2<tm1(cre)Sor>/?,Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul/?	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	16007139
MGI:3615297	M	MP:0002286	cryptorchism	Ret<tm11(RET)Jmi>/Ret<tm11(RET)Jmi>	involves: 129X1/SvJ * 129S1/Sv * C57BL/6	N	16452504
MGI:3615297	F	MP:0011727	ectopic ovary	Ret<tm11(RET)Jmi>/Ret<tm11(RET)Jmi>	involves: 129X1/SvJ * 129S1/Sv * C57BL/6	N	16452504
MGI:3615299	M	MP:0002769	abnormal vas deferens morphology	Ret<tm8(RET)Jmi>/Ret<tm8(RET)Jmi>	involves: 129X1/SvJ * 129S1/Sv * C57BL/6	N	16452504
MGI:3615299	F	MP:0011727	ectopic ovary	Ret<tm8(RET)Jmi>/Ret<tm8(RET)Jmi>	involves: 129X1/SvJ * 129S1/Sv * C57BL/6	N	16452504
MGI:3615299	M	MP:0011410	ectopic testis	Ret<tm8(RET)Jmi>/Ret<tm8(RET)Jmi>	involves: 129X1/SvJ * 129S1/Sv * C57BL/6	N	16452504
MGI:3615332	F	MP:0001923	reduced female fertility	Adcyap1r1<tm1Bbt>/Adcyap1r1<+>	involves: 129 * C57BL/6J	N	11193864
MGI:3615357	M	MP:0020137	decreased bone mineralization	Lrp5<tm1Grw>/Lrp5<tm1Grw>	involves: 129S1/Sv * 129X1/SvJ	N	24225945
MGI:3615360	F	MP:0001386	abnormal maternal nurturing	Gnal<tm1Rax>/Gnal<tm1Rax>	involves: 129/Sv * C57BL/6	N	9459443
MGI:3615360	F	MP:0009326	absent maternal crouching	Gnal<tm1Rax>/Gnal<tm1Rax>	involves: 129/Sv * C57BL/6	N	9459443
MGI:3615360	F	MP:0001384	abnormal pup retrieval	Gnal<tm1Rax>/Gnal<tm1Rax>	involves: 129/Sv * C57BL/6	N	9459443
MGI:3615463	M	MP:0006415	absent testes	Osr1<tm1Jian>/Osr1<tm1Jian>	either: (involves: 129S1/Sv * C57BL/6J) or (involves: 129S1/Sv * ICR)	N	16223478
MGI:3615463	F	MP:0003578	absent ovary	Osr1<tm1Jian>/Osr1<tm1Jian>	either: (involves: 129S1/Sv * C57BL/6J) or (involves: 129S1/Sv * ICR)	N	16223478
MGI:3615575	M	MP:0002675	asthenozoospermia	Hmgb2<tm1Meb>/Hmgb2<tm1Meb>	Not Specified	N	11262228
MGI:3615575	M	MP:0005578	teratozoospermia	Hmgb2<tm1Meb>/Hmgb2<tm1Meb>	Not Specified	N	11262228
MGI:3615575	M	MP:0002216	abnormal seminiferous tubule morphology	Hmgb2<tm1Meb>/Hmgb2<tm1Meb>	Not Specified	N	11262228
MGI:3615575	M	MP:0002286	cryptorchism	Hmgb2<tm1Meb>/Hmgb2<tm1Meb>	Not Specified	N	11262228
MGI:3615575	M	MP:0002784	abnormal Sertoli cell morphology	Hmgb2<tm1Meb>/Hmgb2<tm1Meb>	Not Specified	N	11262228
MGI:3615575	M	MP:0020550	multinucleated giant male germ cells	Hmgb2<tm1Meb>/Hmgb2<tm1Meb>	Not Specified	N	11262228
MGI:3615575	M	MP:0001922	reduced male fertility	Hmgb2<tm1Meb>/Hmgb2<tm1Meb>	Not Specified	N	11262228
MGI:3615575	M	MP:0001146	abnormal testis morphology	Hmgb2<tm1Meb>/Hmgb2<tm1Meb>	Not Specified	N	11262228
MGI:3615660	M	MP:0008404	increased cellular sensitivity to methylmethanesulfonate	Smc1a<tm1Mbk>/Y	involves: 129S1/Sv * C57BL/6	N	15175241
MGI:3615660	M	MP:0004227	increased cellular sensitivity to ionizing radiation	Smc1a<tm1Mbk>/Y	involves: 129S1/Sv * C57BL/6	N	15175241
MGI:3615660	M	MP:0000313	abnormal cell death	Smc1a<tm1Mbk>/Y	involves: 129S1/Sv * C57BL/6	N	15175241
MGI:3615660	M	MP:0004028	chromosome breakage	Smc1a<tm1Mbk>/Y	involves: 129S1/Sv * C57BL/6	N	15175241
MGI:3615660	M	MP:0004045	abnormal cell cycle checkpoint function	Smc1a<tm1Mbk>/Y	involves: 129S1/Sv * C57BL/6	N	15175241
MGI:3615667	M	MP:0002686	globozoospermia	Del(19Poll-Dcpd)1Nmt/Del(19Poll-Dcpd)1Nmt	involves: 129P2/OlaHsd	N	11909969
MGI:3615667	M	MP:0001156	abnormal spermatogenesis	Del(19Poll-Dcpd)1Nmt/Del(19Poll-Dcpd)1Nmt	involves: 129P2/OlaHsd	N	11909969
MGI:3615667	M	MP:0001925	male infertility	Del(19Poll-Dcpd)1Nmt/Del(19Poll-Dcpd)1Nmt	involves: 129P2/OlaHsd	N	11909969
MGI:3615667	M	MP:0002675	asthenozoospermia	Del(19Poll-Dcpd)1Nmt/Del(19Poll-Dcpd)1Nmt	involves: 129P2/OlaHsd	N	11909969
MGI:3615667	M	MP:0006380	abnormal spermatid morphology	Del(19Poll-Dcpd)1Nmt/Del(19Poll-Dcpd)1Nmt	involves: 129P2/OlaHsd	N	11909969
MGI:3615667	M	MP:0005578	teratozoospermia	Del(19Poll-Dcpd)1Nmt/Del(19Poll-Dcpd)1Nmt	involves: 129P2/OlaHsd	N	11909969
MGI:3615687	F	MP:0005089	decreased double-negative T cell number	Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	N	16357220
MGI:3615687	F	MP:0005432	abnormal pro-B cell morphology	Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	N	16357220
MGI:3615687	F	MP:0002083	premature death	Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	N	16357220
MGI:3615687	F	MP:0001577	anemia	Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	N	16357220
MGI:3615687	F	MP:0003884	decreased macrophage cell number	Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	N	16357220
MGI:3615687	F	MP:0002396	abnormal hematopoietic system morphology/development	Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	N	16357220
MGI:3615761	F	MP:0001386	abnormal maternal nurturing	Grm1<rcw-4J>/Grm1<rcw-4J>	C57BL/6J-Grm1<rcw-4J>/GrsrJ	N	MGI:3612952
MGI:3615761	M	MP:0002566	abnormal sexual interaction	Grm1<rcw-4J>/Grm1<rcw-4J>	C57BL/6J-Grm1<rcw-4J>/GrsrJ	N	MGI:3612952
MGI:3615762	M	MP:0005159	azoospermia	Hcn2<trls>/Hcn2<trls>	Not Specified	N	MGI:3608683
MGI:3616179	F	MP:0002169	no abnormal phenotype detected	Nkrf<tm1.1Hjh>/Nkrf<tm1.1Hjh>	involves: 129P2/OlaHsd * C57BL/6	N	16354699
MGI:3616180	M	MP:0002169	no abnormal phenotype detected	Nkrf<tm1.1Hjh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	16354699
MGI:3616398	M	MP:0001146	abnormal testis morphology	Lrat<tm1Log>/Lrat<tm1Log>	involves: 129S1/Sv * C57BL/6J	N	16174770
MGI:3616398	M	MP:0009257	dilated seminiferous tubule	Lrat<tm1Log>/Lrat<tm1Log>	involves: 129S1/Sv * C57BL/6J	N	16174770
MGI:3616398	M	MP:0002687	oligozoospermia	Lrat<tm1Log>/Lrat<tm1Log>	involves: 129S1/Sv * C57BL/6J	N	16174770
MGI:3616398	M	MP:0003205	testicular atrophy	Lrat<tm1Log>/Lrat<tm1Log>	involves: 129S1/Sv * C57BL/6J	N	16174770
MGI:3616398	M	MP:0001940	testis hypoplasia	Lrat<tm1Log>/Lrat<tm1Log>	involves: 129S1/Sv * C57BL/6J	N	16174770
MGI:3616471	M	MP:0001147	small testis	Cenpb<tm1Khac>/Cenpb<tm1Khac>	B6.129-Cenpb<tm1Khac>	N	10645947
MGI:3616471	F	MP:0008028	pregnancy-related premature death	Cenpb<tm1Khac>/Cenpb<tm1Khac>	B6.129-Cenpb<tm1Khac>	N	10645947
MGI:3616471	F	MP:0009096	decreased endometrial gland number	Cenpb<tm1Khac>/Cenpb<tm1Khac>	B6.129-Cenpb<tm1Khac>	N	10645947
MGI:3616471	F	MP:0004014	abnormal uterine environment	Cenpb<tm1Khac>/Cenpb<tm1Khac>	B6.129-Cenpb<tm1Khac>	N	15016956
MGI:3616471	F	MP:0001121	uterus hypoplasia	Cenpb<tm1Khac>/Cenpb<tm1Khac>	B6.129-Cenpb<tm1Khac>	N	10645947
MGI:3616471	F	MP:0003699	abnormal female reproductive system physiology	Cenpb<tm1Khac>/Cenpb<tm1Khac>	B6.129-Cenpb<tm1Khac>	N	10645947
MGI:3616471	F	MP:0001119	abnormal female reproductive system morphology	Cenpb<tm1Khac>/Cenpb<tm1Khac>	B6.129-Cenpb<tm1Khac>	N	10645947
MGI:3616471	F	MP:0004014	abnormal uterine environment	Cenpb<tm1Khac>/Cenpb<tm1Khac>	B6.129-Cenpb<tm1Khac>	N	10645947
MGI:3616471	F	MP:0001120	abnormal uterus morphology	Cenpb<tm1Khac>/Cenpb<tm1Khac>	B6.129-Cenpb<tm1Khac>	N	10645947
MGI:3616471	F	MP:0012008	delayed parturition	Cenpb<tm1Khac>/Cenpb<tm1Khac>	B6.129-Cenpb<tm1Khac>	N	10645947
MGI:3616471	F	MP:0001120	abnormal uterus morphology	Cenpb<tm1Khac>/Cenpb<tm1Khac>	B6.129-Cenpb<tm1Khac>	N	15016956
MGI:3616471	F	MP:0004896	abnormal endometrium morphology	Cenpb<tm1Khac>/Cenpb<tm1Khac>	B6.129-Cenpb<tm1Khac>	N	10645947
MGI:3616471	F	MP:0002292	abnormal gestational length	Cenpb<tm1Khac>/Cenpb<tm1Khac>	B6.129-Cenpb<tm1Khac>	N	10645947
MGI:3616771	F	MP:0003126	abnormal external female genitalia morphology	Chd7<Whi>/Chd7<+>	involves: C3HeB/FeJ	N	16207732
MGI:3616771	F	MP:0009101	clitoris hypoplasia	Chd7<Whi>/Chd7<+>	involves: C3HeB/FeJ	N	16207732
MGI:3616772	F	MP:0003126	abnormal external female genitalia morphology	Chd7<Flo>/Chd7<+>	involves: C3HeB/FeJ	N	16207732
MGI:3616772	F	MP:0009101	clitoris hypoplasia	Chd7<Flo>/Chd7<+>	involves: C3HeB/FeJ	N	16207732
MGI:3616773	F	MP:0003126	abnormal external female genitalia morphology	Crsl/Crsl<+>	involves: C3HeB/FeJ	N	16207732
MGI:3616773	F	MP:0009101	clitoris hypoplasia	Crsl/Crsl<+>	involves: C3HeB/FeJ	N	16207732
MGI:3616875	M	MP:0001925	male infertility	Sptbn4<qv-lnd>/Sptbn4<qv-lnd>	B6.B10-Sptbn4<qv-lnd>	N	1634998
MGI:3617189	M	MP:0000249	abnormal blood vessel physiology	Nox1<tm1Kkr>/Y	B6.129X1-Nox1<tm1Kkr>	N	16386251
MGI:3617189	M	MP:0000272	abnormal aorta morphology	Nox1<tm1Kkr>/Y	B6.129X1-Nox1<tm1Kkr>	N	16386251
MGI:3617189	M	MP:0005319	abnormal enzyme/coenzyme level	Nox1<tm1Kkr>/Y	B6.129X1-Nox1<tm1Kkr>	N	16386251
MGI:3617189	M	MP:0006264	decreased systemic arterial systolic blood pressure	Nox1<tm1Kkr>/Y	B6.129X1-Nox1<tm1Kkr>	N	16386251
MGI:3617198	M	MP:0004933	abnormal epididymis epithelium morphology	Manba<tm1Khf>/Manba<tm1Khf>	B6.129-Manba<tm1Khf>	N	16377659
MGI:3617230	F	MP:0005387	immune system phenotype	Btk<tm1Witt>/Btk<tm1Wk>	involves: 129S4/SvJae * 129X1/SvJ	Y	16291652
MGI:3617307	M	MP:0002182	abnormal astrocyte morphology	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617307	M	MP:0005281	increased fatty acids level	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617307	M	MP:0000920	abnormal myelination	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617307	M	MP:0008295	abnormal adrenal gland zona reticularis morphology	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617307	M	MP:0005405	axon degeneration	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617307	M	MP:0005403	abnormal nerve conduction	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617307	M	MP:0003633	abnormal nervous system physiology	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617307	M	MP:0008294	abnormal adrenal gland zona fasciculata morphology	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617307	M	MP:0008288	abnormal adrenal cortex morphology	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617307	M	MP:0003354	astrocytosis	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617307	M	MP:0000955	abnormal spinal cord morphology	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617307	M	MP:0000136	abnormal microglial cell morphology	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617307	M	MP:0001405	impaired coordination	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617307	M	MP:0003313	abnormal locomotor activation	Abcd1<tm1Kds>/Y	involves: 129S4/SvJae * C57BL/6J	N	15489218
MGI:3617309	M	MP:0002757	decreased vertical activity	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	16223892
MGI:3617309	M	MP:0003633	abnormal nervous system physiology	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	15489218
MGI:3617309	M	MP:0002272	abnormal nervous system electrophysiology	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	16223892
MGI:3617309	M	MP:0001393	ataxia	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	16223892
MGI:3617309	M	MP:0003492	abnormal involuntary movement	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	16223892
MGI:3617309	M	MP:0001504	abnormal posture	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	16223892
MGI:3617309	M	MP:0005405	axon degeneration	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	15489218
MGI:3617309	M	MP:0000952	abnormal CNS glial cell morphology	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	16223892
MGI:3617309	M	MP:0005403	abnormal nerve conduction	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	15489218
MGI:3617309	M	MP:0001525	impaired balance	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	16223892
MGI:3617309	M	MP:0002182	abnormal astrocyte morphology	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	15489218
MGI:3617309	M	MP:0000745	tremors	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	16223892
MGI:3617309	M	MP:0000136	abnormal microglial cell morphology	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	15489218
MGI:3617309	M	MP:0001405	impaired coordination	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	15489218
MGI:3617309	M	MP:0003313	abnormal locomotor activation	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	15489218
MGI:3617309	M	MP:0005281	increased fatty acids level	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	15489218
MGI:3617309	M	MP:0001846	increased inflammatory response	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	15489218
MGI:3617309	M	MP:0005281	increased fatty acids level	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	16223892
MGI:3617309	M	MP:0001392	abnormal locomotor behavior	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	16223892
MGI:3617309	M	MP:0003354	astrocytosis	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	15489218
MGI:3617309	M	MP:0008288	abnormal adrenal cortex morphology	Abcd1<tm1Kds>/Y,Abcd2<tm1Apuj>/Abcd2<tm1Apuj>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	15489218
MGI:3617361	F	MP:0002665	decreased circulating corticosterone level	Hmgn1<tm1Mbus>/Hmgn1<tm1Mbus>	involves: 129X1/SvJ	N	23620591
MGI:3618144	M	MP:0001152	increased Leydig cell number	E2f6<tm1Sgau>/E2f6<tm1Sgau>	involves: 129S4/SvJae * C57BL/6	N	12101104
MGI:3618144	M	MP:0002687	oligozoospermia	E2f6<tm1Sgau>/E2f6<tm1Sgau>	involves: 129S4/SvJae * C57BL/6	N	12101104
MGI:3618185	F	MP:0004047	abnormal milk composition	Plin2<tm1Chan>/Plin2<tm1Chan>	B6.129-Plin2<tm1Chan>	N	17921437
MGI:3618214	F	MP:0001386	abnormal maternal nurturing	Gabra1<tm2.1Geh>/Gabra1<+>	involves: 129X1/SvJ * C57BL/6J	N	15660664
MGI:3618223	F	MP:0013785	abnormal mammary gland bud morphology	Gli3<Xt-J>/Gli3<Xt-J>	involves: C3H/HeJ * C57BL/6	N	16914490
MGI:3618230	F	MP:0001923	reduced female fertility	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	15956199
MGI:3618230	F	MP:0001125	abnormal oocyte morphology	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	15956199
MGI:3618230	F	MP:0005168	abnormal female meiosis	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	15956199
MGI:3618230	F	MP:0001931	abnormal oogenesis	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	15956199
MGI:3618230	F	MP:0003699	abnormal female reproductive system physiology	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	15956199
MGI:3618230	F	MP:0009007	short estrous cycle	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	N	15956199
MGI:3618240	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Atp7a<Mo-Tohm>/Y	involves: AA * C3H/He * C57BL/6 * ICR	N	16338116
MGI:3618240	M	MP:0003952	abnormal copper level	Atp7a<Mo-Tohm>/Y	involves: AA * C3H/He * C57BL/6 * ICR	N	16338116
MGI:3618240	M	MP:0001718	abnormal visceral yolk sac morphology	Atp7a<Mo-Tohm>/Y	involves: AA * C3H/He * C57BL/6 * ICR	N	16338116
MGI:3618241	F	MP:0010768	mortality/aging	Atp7a<Mo-Tohm>/Atp7a<+>	involves: AA * C3H/He * C57BL/6 * ICR	Y	16338116
MGI:3618241	F	MP:0000421	mottled coat	Atp7a<Mo-Tohm>/Atp7a<+>	involves: AA * C3H/He * C57BL/6 * ICR	N	16338116
MGI:3618242	M	MP:0001914	hemorrhage	Atp7a<Mo-Tohm>/Y	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618242	M	MP:0004076	abnormal vitelline vascular remodeling	Atp7a<Mo-Tohm>/Y	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618242	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Atp7a<Mo-Tohm>/Y	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618242	M	MP:0003229	abnormal vitelline vasculature morphology	Atp7a<Mo-Tohm>/Y	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618242	M	MP:0001718	abnormal visceral yolk sac morphology	Atp7a<Mo-Tohm>/Y	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618244	F	MP:0000421	mottled coat	Atp7a<Mo-Tohm>/Atp7a<+>	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618244	F	MP:0003211	abnormal aorta elastic fiber morphology	Atp7a<Mo-Tohm>/Atp7a<+>	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618244	F	MP:0000886	abnormal cerebellar granule layer morphology	Atp7a<Mo-Tohm>/Atp7a<+>	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618244	F	MP:0000815	abnormal Ammon gyrus morphology	Atp7a<Mo-Tohm>/Atp7a<+>	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618244	F	MP:0000788	abnormal cerebral cortex morphology	Atp7a<Mo-Tohm>/Atp7a<+>	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618244	F	MP:0002066	abnormal motor capabilities/coordination/movement	Atp7a<Mo-Tohm>/Atp7a<+>	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618244	F	MP:0014178	increased brain apoptosis	Atp7a<Mo-Tohm>/Atp7a<+>	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618244	F	MP:0000877	abnormal Purkinje cell morphology	Atp7a<Mo-Tohm>/Atp7a<+>	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618244	F	MP:0011215	decreased brain copper level	Atp7a<Mo-Tohm>/Atp7a<+>	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618244	F	MP:0001732	postnatal growth retardation	Atp7a<Mo-Tohm>/Atp7a<+>	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618244	F	MP:0011086	postnatal lethality, incomplete penetrance	Atp7a<Mo-Tohm>/Atp7a<+>	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618244	F	MP:0001914	hemorrhage	Atp7a<Mo-Tohm>/Atp7a<+>	B6.Cg-Atp7a<Mo-Tohm>	N	16338116
MGI:3618273	M	MP:0004924	abnormal behavior	Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * Black Swiss	N	12196578
MGI:3618273	M	MP:0002083	premature death	Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * Black Swiss	N	12196578
MGI:3618273	M	MP:0011086	postnatal lethality, incomplete penetrance	Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * Black Swiss	N	12196578
MGI:3618273	M	MP:0001265	decreased body size	Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * Black Swiss	N	12196578
MGI:3618273	M	MP:0000807	abnormal hippocampus morphology	Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * Black Swiss	N	12196578
MGI:3618273	M	MP:0008284	abnormal hippocampus pyramidal cell layer	Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * Black Swiss	N	12196578
MGI:3618273	M	MP:0001922	reduced male fertility	Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * Black Swiss	N	12196578
MGI:3618275	F	MP:0010053	decreased grip strength	Dcx<tm1Caw>/Dcx<+>	involves: 129S6/SvEvTac * 129X1/SvJ * Black Swiss	N	12196578
MGI:3618275	F	MP:0001462	abnormal avoidance learning behavior	Dcx<tm1Caw>/Dcx<+>	involves: 129S6/SvEvTac * 129X1/SvJ * Black Swiss	N	12196578
MGI:3618275	F	MP:0008284	abnormal hippocampus pyramidal cell layer	Dcx<tm1Caw>/Dcx<+>	involves: 129S6/SvEvTac * 129X1/SvJ * Black Swiss	N	12196578
MGI:3618275	F	MP:0000807	abnormal hippocampus morphology	Dcx<tm1Caw>/Dcx<+>	involves: 129S6/SvEvTac * 129X1/SvJ * Black Swiss	N	12196578
MGI:3618278	F	MP:0001926	female infertility	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	N	15659488
MGI:3618278	F	MP:0001119	abnormal female reproductive system morphology	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	N	15659488
MGI:3618278	F	MP:0001130	abnormal ovarian folliculogenesis	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	N	15659488
MGI:3618278	F	MP:0001127	small ovary	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	N	15659488
MGI:3618278	F	MP:0005168	abnormal female meiosis	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	N	15659488
MGI:3618278	F	MP:0001129	impaired ovarian folliculogenesis	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	N	15659488
MGI:3618278	F	MP:0001125	abnormal oocyte morphology	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	N	15659488
MGI:3618278	F	MP:0001131	abnormal ovarian follicle morphology	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	N	15659488
MGI:3618280	F	MP:0001463	abnormal spatial learning	Dcx<tm1Caw>/Dcx<+>	involves: 129S6/SvEvTac * 129X1/SvJ	N	12196578
MGI:3618280	F	MP:0010053	decreased grip strength	Dcx<tm1Caw>/Dcx<+>	involves: 129S6/SvEvTac * 129X1/SvJ	N	12196578
MGI:3618280	F	MP:0001462	abnormal avoidance learning behavior	Dcx<tm1Caw>/Dcx<+>	involves: 129S6/SvEvTac * 129X1/SvJ	N	12196578
MGI:3618293	M	MP:0001922	reduced male fertility	Ace<tm1Keb>/Ace<tm1Keb>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	8642790
MGI:3618307	M	MP:0000790	abnormal stratification in cerebral cortex	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618307	M	MP:0011085	postnatal lethality, complete penetrance	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618307	M	MP:0008225	abnormal anterior commissure morphology	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618307	M	MP:0002196	absent corpus callosum	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618308	M	MP:0002882	abnormal neuron morphology	Dclk1<tm1.1Jgg>/Dclk1<+>,Dcx<tm1Caw>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618308	M	MP:0008226	decreased anterior commissure size	Dclk1<tm1.1Jgg>/Dclk1<+>,Dcx<tm1Caw>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618308	M	MP:0000780	abnormal corpus callosum morphology	Dclk1<tm1.1Jgg>/Dclk1<+>,Dcx<tm1Caw>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618309	F	MP:0008227	absent anterior commissure	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618309	F	MP:0008223	absent hippocampal commissure	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618309	F	MP:0011085	postnatal lethality, complete penetrance	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618309	F	MP:0002199	abnormal brain commissure morphology	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618309	F	MP:0000790	abnormal stratification in cerebral cortex	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618309	F	MP:0002882	abnormal neuron morphology	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618309	F	MP:0002196	absent corpus callosum	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618310	F	MP:0002196	absent corpus callosum	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Dcx<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618310	F	MP:0000790	abnormal stratification in cerebral cortex	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Dcx<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618310	F	MP:0008225	abnormal anterior commissure morphology	Dclk1<tm1.1Jgg>/Dclk1<tm1.1Jgg>,Dcx<tm1Caw>/Dcx<+>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618311	F	MP:0002196	absent corpus callosum	Dclk1<tm1.1Jgg>/Dclk1<+>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	N	16387639
MGI:3618357	F	MP:0012010	parturition failure	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	N	10508513
MGI:3618538	F	MP:0001120	abnormal uterus morphology	Prkce<tm1Bsca>/Prkce<tm1Bsca>	involves: 129P2/OlaHsd * C57BL/6	N	11696589
MGI:3618538	F	MP:0001123	dilated uterus	Prkce<tm1Bsca>/Prkce<tm1Bsca>	involves: 129P2/OlaHsd * C57BL/6	N	11696589
MGI:3618538	F	MP:0001923	reduced female fertility	Prkce<tm1Bsca>/Prkce<tm1Bsca>	involves: 129P2/OlaHsd * C57BL/6	N	11696589
MGI:3618597	F	MP:0001729	impaired embryo implantation	Nos3<tm1Unc>/Nos3<tm1Unc>	B6.129P2-Nos3<tm1Unc>/J	N	18663015
MGI:3618597	F	MP:0002680	decreased corpora lutea number	Nos3<tm1Unc>/Nos3<tm1Unc>	B6.129P2-Nos3<tm1Unc>/J	N	18663015
MGI:3618597	F	MP:0008869	anovulation	Nos3<tm1Unc>/Nos3<tm1Unc>	B6.129P2-Nos3<tm1Unc>/J	N	18663015
MGI:3618597	F	MP:0001126	abnormal ovary morphology	Nos3<tm1Unc>/Nos3<tm1Unc>	B6.129P2-Nos3<tm1Unc>/J	N	18663015
MGI:3618597	F	MP:0003355	decreased ovulation rate	Nos3<tm1Unc>/Nos3<tm1Unc>	B6.129P2-Nos3<tm1Unc>/J	N	18663015
MGI:3618597	F	MP:0001127	small ovary	Nos3<tm1Unc>/Nos3<tm1Unc>	B6.129P2-Nos3<tm1Unc>/J	N	18663015
MGI:3618597	F	MP:0009661	abnormal pregnancy	Nos3<tm1Unc>/Nos3<tm1Unc>	B6.129P2-Nos3<tm1Unc>/J	N	18663015
MGI:3618629	F	MP:0000694	spleen hypoplasia	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0001700	abnormal embryo turning	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0010808	right-sided stomach	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0003036	vertebral transformation	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000783	abnormal forebrain morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0010402	ventricular septal defect	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0001706	abnormal left-right axis patterning	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0020530	disorganized thalamus	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000531	right pulmonary isomerism	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0006007	abnormal basal ganglion morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000850	absent cerebellum	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0011101	prenatal lethality, incomplete penetrance	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000150	abnormal rib morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0004157	interrupted aortic arch	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000807	abnormal hippocampus morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0001890	anencephaly	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000269	abnormal heart looping	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0003984	embryonic growth retardation	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000788	abnormal cerebral cortex morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0002621	delayed neural tube closure	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0003178	left pulmonary isomerism	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000914	exencephaly	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000598	abnormal liver morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000137	abnormal vertebrae morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0011086	postnatal lethality, incomplete penetrance	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000267	abnormal heart development	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0002127	abnormal cardiovascular system morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0002114	abnormal axial skeleton morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000830	abnormal diencephalon morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0004158	right aortic arch	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000929	open neural tube	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0005236	abnormal olfactory nerve morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0010854	lung situs inversus	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0011665	d-loop transposition of the great arteries	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0000897	abnormal midbrain morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0010403	atrial septal defect	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618629	F	MP:0006065	abnormal heart position or orientation	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000830	abnormal diencephalon morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0004158	right aortic arch	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0004157	interrupted aortic arch	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0002621	delayed neural tube closure	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0010402	ventricular septal defect	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0010403	atrial septal defect	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000807	abnormal hippocampus morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0003178	left pulmonary isomerism	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0003036	vertebral transformation	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000269	abnormal heart looping	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000788	abnormal cerebral cortex morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000267	abnormal heart development	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0002114	abnormal axial skeleton morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0002127	abnormal cardiovascular system morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000585	kinked tail	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0001706	abnormal left-right axis patterning	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0001700	abnormal embryo turning	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0006065	abnormal heart position or orientation	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0011086	postnatal lethality, incomplete penetrance	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000914	exencephaly	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0001890	anencephaly	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0011665	d-loop transposition of the great arteries	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0011101	prenatal lethality, incomplete penetrance	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000531	right pulmonary isomerism	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000137	abnormal vertebrae morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000598	abnormal liver morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000150	abnormal rib morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0003984	embryonic growth retardation	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0006007	abnormal basal ganglion morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000783	abnormal forebrain morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0010808	right-sided stomach	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000694	spleen hypoplasia	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0005236	abnormal olfactory nerve morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0010854	lung situs inversus	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000897	abnormal midbrain morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000929	open neural tube	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0020530	disorganized thalamus	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618630	M	MP:0000850	absent cerebellum	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000897	abnormal midbrain morphology	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000807	abnormal hippocampus morphology	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0011665	d-loop transposition of the great arteries	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000929	open neural tube	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000598	abnormal liver morphology	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000267	abnormal heart development	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000150	abnormal rib morphology	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0004157	interrupted aortic arch	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0002621	delayed neural tube closure	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000531	right pulmonary isomerism	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000914	exencephaly	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0003984	embryonic growth retardation	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0011086	postnatal lethality, incomplete penetrance	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000788	abnormal cerebral cortex morphology	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000269	abnormal heart looping	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0001890	anencephaly	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0006007	abnormal basal ganglion morphology	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000830	abnormal diencephalon morphology	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0002127	abnormal cardiovascular system morphology	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000585	kinked tail	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0003036	vertebral transformation	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000783	abnormal forebrain morphology	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000137	abnormal vertebrae morphology	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0006065	abnormal heart position or orientation	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0002114	abnormal axial skeleton morphology	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000850	absent cerebellum	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0005236	abnormal olfactory nerve morphology	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0010402	ventricular septal defect	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0004158	right aortic arch	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0000694	spleen hypoplasia	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0020530	disorganized thalamus	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0010808	right-sided stomach	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0010403	atrial septal defect	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0001706	abnormal left-right axis patterning	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0003178	left pulmonary isomerism	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0001700	abnormal embryo turning	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618631	F	MP:0010854	lung situs inversus	Zic3<tm1Bca>/Zic3<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11959836
MGI:3618632	M	MP:0011101	prenatal lethality, incomplete penetrance	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * Swiss	N	11959836
MGI:3618633	F	MP:0004073	caudal body truncation	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0004559	small allantois	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0004713	split notochord	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0001695	abnormal gastrulation	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0009331	absent primitive node	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0005224	abnormal left-right axis symmetry of the somites	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0001730	embryonic growth arrest	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0005221	abnormal rostral-caudal axis patterning	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0012739	abnormal anterior primitive streak morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0002231	abnormal primitive streak morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0001688	abnormal somite development	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0001680	abnormal mesoderm development	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0001706	abnormal left-right axis patterning	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0011092	embryonic lethality, complete penetrance	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0008533	abnormal anterior visceral endoderm morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0000786	abnormal embryonic neuroepithelial layer differentiation	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0003886	abnormal embryonic epiblast morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0012156	rostral-caudal axis duplication	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0000269	abnormal heart looping	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0003984	embryonic growth retardation	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0002085	abnormal embryonic tissue morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0002086	abnormal extraembryonic tissue morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0005657	abnormal neural plate morphology	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618633	F	MP:0001672	abnormal embryo development	Zic3<tm1Bca>/Zic3<tm1Bca>	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0011092	embryonic lethality, complete penetrance	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0008533	abnormal anterior visceral endoderm morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0012156	rostral-caudal axis duplication	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0001688	abnormal somite development	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0003886	abnormal embryonic epiblast morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0003984	embryonic growth retardation	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0009331	absent primitive node	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0012685	abnormal primitive streak elongation	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0004073	caudal body truncation	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0000269	abnormal heart looping	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0005221	abnormal rostral-caudal axis patterning	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0001706	abnormal left-right axis patterning	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0012739	abnormal anterior primitive streak morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0001695	abnormal gastrulation	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0001730	embryonic growth arrest	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0005224	abnormal left-right axis symmetry of the somites	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0002086	abnormal extraembryonic tissue morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0005657	abnormal neural plate morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0001672	abnormal embryo development	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0002231	abnormal primitive streak morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0004713	split notochord	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0002085	abnormal embryonic tissue morphology	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0001680	abnormal mesoderm development	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0004559	small allantois	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618634	M	MP:0000786	abnormal embryonic neuroepithelial layer differentiation	Zic3<tm1Bca>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16397896
MGI:3618687	M	MP:0001925	male infertility	Ercc1<tm1Dwm>/Ercc1<tm1Dwm>,Tg(Ttr-Ercc1)17Dwm/0	involves: 129P2/OlaHsd * BALB/c	N	12466203
MGI:3618687	F	MP:0011126	absent primary ovarian follicles	Ercc1<tm1Dwm>/Ercc1<tm1Dwm>,Tg(Ttr-Ercc1)17Dwm/0	involves: 129P2/OlaHsd * BALB/c	N	12466203
MGI:3618687	M	MP:0008280	abnormal male germ cell apoptosis	Ercc1<tm1Dwm>/Ercc1<tm1Dwm>,Tg(Ttr-Ercc1)17Dwm/0	involves: 129P2/OlaHsd * BALB/c	N	12466203
MGI:3618687	M	MP:0001156	abnormal spermatogenesis	Ercc1<tm1Dwm>/Ercc1<tm1Dwm>,Tg(Ttr-Ercc1)17Dwm/0	involves: 129P2/OlaHsd * BALB/c	N	12466203
MGI:3618687	F	MP:0001130	abnormal ovarian folliculogenesis	Ercc1<tm1Dwm>/Ercc1<tm1Dwm>,Tg(Ttr-Ercc1)17Dwm/0	involves: 129P2/OlaHsd * BALB/c	N	12466203
MGI:3618687	F	MP:0001926	female infertility	Ercc1<tm1Dwm>/Ercc1<tm1Dwm>,Tg(Ttr-Ercc1)17Dwm/0	involves: 129P2/OlaHsd * BALB/c	N	12466203
MGI:3618821	M	MP:0004031	insulitis	X/Tg(Ins2-GAD2)1Lt	NOD/ShiLt-Tg(Ins2-GAD2)1Lt	N	9836515
MGI:3618856	F	MP:0004502	decreased incidence of tumors by chemical induction	Modc2<BALB/cJ>/Modc2<BALB/cJ>	involves: BALB/cJ * C57BL/6J	N	16086382
MGI:3618857	F	MP:0004502	decreased incidence of tumors by chemical induction	Modc2<BALB/cJ>/Modc2<C57BL/6J>	involves: BALB/cJ * C57BL/6J	N	16086382
MGI:3618868	M	MP:0005668	decreased circulating leptin level	Eif4ebp1<tm1Nso>/Eif4ebp1<tm1Nso>	involves: 129S4/SvJae * BALB/c	N	11590436
MGI:3618868	M	MP:0009283	decreased gonadal fat pad weight	Eif4ebp1<tm1Nso>/Eif4ebp1<tm1Nso>	involves: 129S4/SvJae * BALB/c	N	11590436
MGI:3618868	M	MP:0005289	increased oxygen consumption	Eif4ebp1<tm1Nso>/Eif4ebp1<tm1Nso>	involves: 129S4/SvJae * BALB/c	N	11590436
MGI:3618868	M	MP:0005670	abnormal white adipose tissue physiology	Eif4ebp1<tm1Nso>/Eif4ebp1<tm1Nso>	involves: 129S4/SvJae * BALB/c	N	11590436
MGI:3618868	M	MP:0001262	decreased body weight	Eif4ebp1<tm1Nso>/Eif4ebp1<tm1Nso>	involves: 129S4/SvJae * BALB/c	N	11590436
MGI:3618892	F	MP:0001132	absent mature ovarian follicles	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	N	10915769
MGI:3618892	F	MP:0001126	abnormal ovary morphology	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	N	10915769
MGI:3618892	M	MP:0001922	reduced male fertility	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	N	10915769
MGI:3618892	F	MP:0001923	reduced female fertility	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	N	10915769
MGI:3618892	M	MP:0001153	small seminiferous tubules	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	N	10915769
MGI:3618892	M	MP:0001156	abnormal spermatogenesis	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	N	10915769
MGI:3618892	M	MP:0001152	increased Leydig cell number	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	N	10915769
MGI:3619123	F	MP:0031420	decreased superovulation rate	Agt<tm2Unc>/Agt<+>	involves: 129P2/OlaHsd * C57BL/6J	N	11384650
MGI:3619131	F	MP:0031420	decreased superovulation rate	Agt<tm2Unc>/Agt<tm2Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11384650
MGI:3619217	F	MP:0001874	acanthosis	Piga<tm1Tak>/Piga<+>,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	9207103
MGI:3619217	F	MP:0001192	scaly skin	Piga<tm1Tak>/Piga<+>,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	9207103
MGI:3619350	F	MP:0001926	female infertility	Piga<tm1Tak>/Piga<tm1Tak>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ	N	12692150
MGI:3619350	F	MP:0000242	impaired fertilization	Piga<tm1Tak>/Piga<tm1Tak>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ	N	12692150
MGI:3619350	F	MP:0001124	abnormal gametes	Piga<tm1Tak>/Piga<tm1Tak>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ	N	12692150
MGI:3619444	M	MP:0001718	abnormal visceral yolk sac morphology	Piga<tm1.1Tak>/Y	involves: 129S1/Sv * 129X1/SvJ	N	10092065
MGI:3619444	M	MP:0011091	prenatal lethality, complete penetrance	Piga<tm1.1Tak>/Y	involves: 129S1/Sv * 129X1/SvJ	N	10092065
MGI:3619444	M	MP:0001698	decreased embryo size	Piga<tm1.1Tak>/Y	involves: 129S1/Sv * 129X1/SvJ	N	10092065
MGI:3619447	F	MP:0011091	prenatal lethality, complete penetrance	Piga<tm1.1Tak>/Piga<+>	involves: 129S1/Sv * 129X1/SvJ	N	10092065
MGI:3619447	F	MP:0002116	abnormal craniofacial bone morphology	Piga<tm1.1Tak>/Piga<+>	involves: 129S1/Sv * 129X1/SvJ	N	10092065
MGI:3619447	F	MP:0000913	abnormal brain development	Piga<tm1.1Tak>/Piga<+>	involves: 129S1/Sv * 129X1/SvJ	N	10092065
MGI:3619447	F	MP:0000914	exencephaly	Piga<tm1.1Tak>/Piga<+>	involves: 129S1/Sv * 129X1/SvJ	N	10092065
MGI:3619447	F	MP:0000164	abnormal cartilage development	Piga<tm1.1Tak>/Piga<+>	involves: 129S1/Sv * 129X1/SvJ	N	10092065
MGI:3619447	F	MP:0005382	craniofacial phenotype	Piga<tm1.1Tak>/Piga<+>	involves: 129S1/Sv * 129X1/SvJ	Y	10092065
MGI:3619514	M	MP:0001364	decreased anxiety-related response	Avpr1a<tm1Sbhu>/Avpr1a<tm1Sbhu>	129X1.Cg-Avpr1a<tm1Sbhu>	N	14647484
MGI:3619514	M	MP:0001360	abnormal social investigation	Avpr1a<tm1Sbhu>/Avpr1a<tm1Sbhu>	129X1.Cg-Avpr1a<tm1Sbhu>	N	14647484
MGI:3619520	F	MP:0008054	abnormal uterine NK cell morphology	Fbn1<Tsk>/Fbn1<+>	B6.Cg-Fbn1<Tsk>	N	1617705
MGI:3619532	F	MP:0005350	increased susceptibility to autoimmune disorder	Muc19<sld>/Muc19<sld>	NFS/N-Muc19<sld>	N	25447050
MGI:3619848	F	MP:0001386	abnormal maternal nurturing	Ing1<tm1Avg>/Ing1<tm1Avg>	involves: 129S1/Sv * C57BL/6	N	16170338
MGI:3620021	F	MP:0001926	female infertility	Car14<tm1Sly>/Car14<tm1Sly>,Car4<tm1Sly>/Car4<tm1Sly>	involves: 129S1/Sv * C57BL/6	N	16260723
MGI:3620063	M	MP:0001925	male infertility	hpc/hpc	involves: 129/Sv * C3H/He	N	6841964
MGI:3620063	F	MP:0001926	female infertility	hpc/hpc	involves: 129/Sv * C3H/He	N	6841964
MGI:3620065	M	MP:0002079	increased circulating insulin level	Neil1<tm1Rsld>/Neil1<tm1Rsld>	involves: 129S1/Sv * C57BL/6	N	16446448
MGI:3620065	M	MP:0000598	abnormal liver morphology	Neil1<tm1Rsld>/Neil1<tm1Rsld>	involves: 129S1/Sv * C57BL/6	N	16446448
MGI:3620087	F	MP:0004047	abnormal milk composition	B4galt1<tm1Yiw>/B4galt1<tm1Yiw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9155011
MGI:3620088	F	MP:0004047	abnormal milk composition	B4galt1<tm1Yiw>/B4galt1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9155011
MGI:3620089	F	MP:0004021	abnormal rod electrophysiology	Chm<tm1.2Seab>/Chm<+>	involves: 129X1/SvJ	N	16410831
MGI:3620089	F	MP:0005103	abnormal retina pigmentation	Chm<tm1.2Seab>/Chm<+>	involves: 129X1/SvJ	N	16410831
MGI:3620089	F	MP:0008587	short photoreceptor outer segment	Chm<tm1.2Seab>/Chm<+>	involves: 129X1/SvJ	N	16410831
MGI:3620089	F	MP:0001325	abnormal retina morphology	Chm<tm1.2Seab>/Chm<+>	involves: 129X1/SvJ	N	16410831
MGI:3620089	F	MP:0003638	abnormal response/metabolism to endogenous compounds	Chm<tm1.2Seab>/Chm<+>	involves: 129X1/SvJ	N	16410831
MGI:3620090	F	MP:0008515	thin retina outer nuclear layer	Chm<tm1.3Seab>/Chm<+>	involves: 129X1/SvJ	N	16410831
MGI:3620090	F	MP:0001325	abnormal retina morphology	Chm<tm1.3Seab>/Chm<+>	involves: 129X1/SvJ	N	16410831
MGI:3620090	F	MP:0003638	abnormal response/metabolism to endogenous compounds	Chm<tm1.3Seab>/Chm<+>	involves: 129X1/SvJ	N	16410831
MGI:3620090	F	MP:0008450	retina photoreceptor degeneration	Chm<tm1.3Seab>/Chm<+>	involves: 129X1/SvJ	N	16410831
MGI:3620090	F	MP:0005103	abnormal retina pigmentation	Chm<tm1.3Seab>/Chm<+>	involves: 129X1/SvJ	N	16410831
MGI:3620090	F	MP:0003729	abnormal photoreceptor outer segment morphology	Chm<tm1.3Seab>/Chm<+>	involves: 129X1/SvJ	N	16410831
MGI:3620090	F	MP:0004021	abnormal rod electrophysiology	Chm<tm1.3Seab>/Chm<+>	involves: 129X1/SvJ	N	16410831
MGI:3620090	F	MP:0005201	abnormal retina pigment epithelium morphology	Chm<tm1.3Seab>/Chm<+>	involves: 129X1/SvJ	N	16410831
MGI:3620091	M	MP:0005376	homeostasis/metabolism phenotype	Chm<tm1Seab>/Y	involves: 129X1/SvJ	Y	16410831
MGI:3620092	M	MP:0002169	no abnormal phenotype detected	Chm<tm1.1Seab>/Y	involves: 129X1/SvJ	N	16410831
MGI:3620093	F	MP:0004021	abnormal rod electrophysiology	Chm<tm1.1Seab>/Chm<tm1.1Seab>,Tg(Six3-cre)69Frty/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	16410831
MGI:3620093	F	MP:0008587	short photoreceptor outer segment	Chm<tm1.1Seab>/Chm<tm1.1Seab>,Tg(Six3-cre)69Frty/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	16410831
MGI:3620093	F	MP:0008515	thin retina outer nuclear layer	Chm<tm1.1Seab>/Chm<tm1.1Seab>,Tg(Six3-cre)69Frty/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	16410831
MGI:3620093	F	MP:0001325	abnormal retina morphology	Chm<tm1.1Seab>/Chm<tm1.1Seab>,Tg(Six3-cre)69Frty/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	16410831
MGI:3620094	M	MP:0008515	thin retina outer nuclear layer	Chm<tm1.1Seab>/Y,Tg(Six3-cre)69Frty/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	16410831
MGI:3620094	M	MP:0004021	abnormal rod electrophysiology	Chm<tm1.1Seab>/Y,Tg(Six3-cre)69Frty/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	16410831
MGI:3620094	M	MP:0001325	abnormal retina morphology	Chm<tm1.1Seab>/Y,Tg(Six3-cre)69Frty/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	16410831
MGI:3620094	M	MP:0008587	short photoreceptor outer segment	Chm<tm1.1Seab>/Y,Tg(Six3-cre)69Frty/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	16410831
MGI:3620105	M	MP:0010357	increased prostate gland tumor incidence	Tg(Pbsn-MYC)6Key/?	involves: FVB	N	14522256
MGI:3620105	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-MYC)6Key/?	involves: FVB	N	14522256
MGI:3620105	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(Pbsn-MYC)6Key/?	involves: FVB	N	14522256
MGI:3620192	F	MP:0005403	abnormal nerve conduction	Plp1<tm1Wst>/Plp1<tm1Wst>	involves: 129P2/OlaHsd	N	7526402
MGI:3620192	F	MP:0000920	abnormal myelination	Plp1<tm1Wst>/Plp1<tm1Wst>	involves: 129P2/OlaHsd	N	7526402
MGI:3620192	F	MP:0001402	decreased locomotor activity	Plp1<tm1Wst>/Plp1<tm1Wst>	involves: 129P2/OlaHsd	N	7526402
MGI:3620192	F	MP:0010047	axonal spheroids	Plp1<tm1Wst>/Plp1<tm1Wst>	involves: 129P2/OlaHsd	N	11746780
MGI:3620192	F	MP:0005404	abnormal axon morphology	Plp1<tm1Wst>/Plp1<tm1Wst>	involves: 129P2/OlaHsd	N	11746780
MGI:3620192	F	MP:0001405	impaired coordination	Plp1<tm1Wst>/Plp1<tm1Wst>	involves: 129P2/OlaHsd	N	7526402
MGI:3620192	F	MP:0003871	abnormal myelin sheath morphology	Plp1<tm1Wst>/Plp1<tm1Wst>	involves: 129P2/OlaHsd	N	11746780
MGI:3620192	F	MP:0000920	abnormal myelination	Plp1<tm1Wst>/Plp1<tm1Wst>	involves: 129P2/OlaHsd	N	11746780
MGI:3620192	F	MP:0000953	abnormal oligodendrocyte morphology	Plp1<tm1Wst>/Plp1<tm1Wst>	involves: 129P2/OlaHsd	N	7526402
MGI:3620193	F	MP:0000953	abnormal oligodendrocyte morphology	Plp1<tm1Wst>/Plp1<+>	involves: 129P2/OlaHsd	N	7526402
MGI:3620194	F	MP:0005403	abnormal nerve conduction	Plp1<tm2Wst>/Plp1<tm2Wst>	involves: 129P2/OlaHsd	N	7526402
MGI:3620194	F	MP:0000953	abnormal oligodendrocyte morphology	Plp1<tm2Wst>/Plp1<tm2Wst>	involves: 129P2/OlaHsd	N	7526402
MGI:3620194	F	MP:0001402	decreased locomotor activity	Plp1<tm2Wst>/Plp1<tm2Wst>	involves: 129P2/OlaHsd	N	7526402
MGI:3620194	F	MP:0000920	abnormal myelination	Plp1<tm2Wst>/Plp1<tm2Wst>	involves: 129P2/OlaHsd	N	7526402
MGI:3620194	F	MP:0001405	impaired coordination	Plp1<tm2Wst>/Plp1<tm2Wst>	involves: 129P2/OlaHsd	N	7526402
MGI:3620195	F	MP:0000953	abnormal oligodendrocyte morphology	Plp1<tm2Wst>/Plp1<+>	involves: 129P2/OlaHsd	N	7526402
MGI:3620196	F	MP:0000920	abnormal myelination	Plp1<tm3Wst>/Plp1<tm3Wst>	B6.129S1-Plp1<tm3Wst>	N	11746780
MGI:3620196	F	MP:0001330	abnormal optic nerve morphology	Plp1<tm3Wst>/Plp1<tm3Wst>	B6.129S1-Plp1<tm3Wst>	N	11746780
MGI:3620196	F	MP:0003871	abnormal myelin sheath morphology	Plp1<tm3Wst>/Plp1<tm3Wst>	B6.129S1-Plp1<tm3Wst>	N	11746780
MGI:3620219	F	MP:0000501	abnormal digestive secretion	P2ry4<tm1Brob>/P2ry4<tm1Brob>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12644577
MGI:3620219	F	MP:0011090	perinatal lethality, incomplete penetrance	P2ry4<tm1Brob>/P2ry4<tm1Brob>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12644577
MGI:3620220	M	MP:0000501	abnormal digestive secretion	P2ry4<tm1Brob>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12644577
MGI:3620241	M	MP:0005386	behavior/neurological phenotype	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	9010205
MGI:3620241	M	MP:0003871	abnormal myelin sheath morphology	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9010205
MGI:3620241	M	MP:0010047	axonal spheroids	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	9010205
MGI:3620242	M	MP:0000921	demyelination	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9616125
MGI:3620242	M	MP:0010047	axonal spheroids	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	28836307
MGI:3620242	M	MP:0003354	astrocytosis	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	28836307
MGI:3620242	M	MP:0003354	astrocytosis	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9616125
MGI:3620242	M	MP:0003312	abnormal locomotor coordination	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9616125
MGI:3620242	M	MP:0000953	abnormal oligodendrocyte morphology	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	15662843
MGI:3620242	M	MP:0000953	abnormal oligodendrocyte morphology	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9616125
MGI:3620242	M	MP:0003005	abnormal hippocampal fimbria morphology	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	28836307
MGI:3620242	M	MP:0003871	abnormal myelin sheath morphology	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9616125
MGI:3620242	M	MP:0003871	abnormal myelin sheath morphology	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	23322581
MGI:3620242	M	MP:0000136	abnormal microglial cell morphology	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9616125
MGI:3620242	M	MP:0001405	impaired coordination	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9616125
MGI:3620242	M	MP:0005404	abnormal axon morphology	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9616125
MGI:3620242	M	MP:0001406	abnormal gait	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	9616125
MGI:3620242	M	MP:0008918	microgliosis	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	28836307
MGI:3620242	M	MP:0003983	decreased cholesterol level	Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ	N	23322581
MGI:3620243	M	MP:0001393	ataxia	Mbp<shi>/Mbp<shi>,Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SWV	N	9010205
MGI:3620243	M	MP:0010768	mortality/aging	Mbp<shi>/Mbp<shi>,Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SWV	Y	9010205
MGI:3620243	M	MP:0003871	abnormal myelin sheath morphology	Mbp<shi>/Mbp<shi>,Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SWV	N	9010205
MGI:3620243	M	MP:0000745	tremors	Mbp<shi>/Mbp<shi>,Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SWV	N	9010205
MGI:3620243	M	MP:0000920	abnormal myelination	Mbp<shi>/Mbp<shi>,Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SWV	N	9010205
MGI:3620245	M	MP:0000921	demyelination	Mbp<shi>/Mbp<shi>,Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * SWV	N	9616125
MGI:3620245	M	MP:0010047	axonal spheroids	Mbp<shi>/Mbp<shi>,Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * SWV	N	9616125
MGI:3620248	F	MP:0005404	abnormal axon morphology	Plp1<tm1Kan>/Plp1<+>	involves: 129S1/Sv * 129X1/SvJ	N	9616125
MGI:3620461	F	MP:0002666	increased circulating aldosterone level	Kcnk3<tm1Sgb>/Kcnk3<tm1Sgb>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22918120
MGI:3620522	M	MP:0013321	squamous metaplasia of seminal vesicles	Rarg<tm3.1Ipc>/Rarg<tm3.1Ipc>	involves: C57BL/6 * SJL	N	11857788
MGI:3620522	M	MP:0001925	male infertility	Rarg<tm3.1Ipc>/Rarg<tm3.1Ipc>	involves: C57BL/6 * SJL	N	11857788
MGI:3620522	M	MP:0013322	squamous metaplasia of prostate gland	Rarg<tm3.1Ipc>/Rarg<tm3.1Ipc>	involves: C57BL/6 * SJL	N	11857788
MGI:3620543	M	MP:0001516	abnormal motor coordination/balance	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0003360	abnormal depression-related behavior	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0001906	increased dopamine level	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0002566	abnormal sexual interaction	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0010069	increased serotonin level	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0001357	increased aggression towards humans	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0012575	increased noradrenaline level	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0001505	hunched posture	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0001354	increased aggression towards male mice	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0002557	abnormal social/conspecific interaction behavior	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0000788	abnormal cerebral cortex morphology	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0001525	impaired balance	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0001360	abnormal social investigation	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0004924	abnormal behavior	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0001410	head bobbing	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0001501	abnormal sleep pattern	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0003459	increased fear-related response	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0001400	hyperresponsive	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0001523	impaired righting response	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0001431	abnormal eating behavior	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620543	M	MP:0001440	abnormal grooming behavior	Maoa<Tg(H2-K1-Ifnb1)8Seif>/Y	involves: C3H/HeJ	N	7792602
MGI:3620623	F	MP:0002123	abnormal definitive hematopoiesis	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	16530702
MGI:3620623	F	MP:0010766	abnormal NK cell physiology	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	12387738
MGI:3620623	F	MP:0002619	abnormal lymphocyte morphology	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	12387738
MGI:3620623	F	MP:0005070	impaired natural killer cell mediated cytotoxicity	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	12387738
MGI:3620623	F	MP:0004809	increased hematopoietic stem cell number	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	16530702
MGI:3620623	F	MP:0002220	large lymphoid organs	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	12387738
MGI:3620623	F	MP:0001845	abnormal inflammatory response	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	12387738
MGI:3620623	F	MP:0003945	abnormal lymphocyte physiology	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	12387738
MGI:3620623	F	MP:0005079	decreased cytotoxic T cell cytolysis	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	12387738
MGI:3620623	F	MP:0005348	increased T cell proliferation	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	12387738
MGI:3620623	F	MP:0008040	decreased NK T cell number	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	12387738
MGI:3620623	F	MP:0005014	increased B cell number	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	12387738
MGI:3620623	F	MP:0008045	decreased NK cell number	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	12387738
MGI:3620623	F	MP:0004808	abnormal hematopoietic stem cell morphology	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	16530702
MGI:3620623	F	MP:0005154	increased B cell proliferation	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	12387738
MGI:3620623	F	MP:0002145	abnormal T cell differentiation	Elf4<tm1Nim>/Elf4<tm1Nim>	B6.129S1-Elf4<tm1Nim>	N	12387738
MGI:3620649	F	MP:0000564	syndactyly	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620649	F	MP:0003641	small lung	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620649	F	MP:0000157	abnormal sternum morphology	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620649	F	MP:0011682	renal glomerulus cyst	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620649	F	MP:0005325	abnormal renal glomerulus morphology	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620649	F	MP:0001614	abnormal blood vessel morphology	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620649	F	MP:0000562	polydactyly	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620649	F	MP:0011087	neonatal lethality, complete penetrance	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620649	F	MP:0002152	abnormal brain morphology	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620649	F	MP:0001698	decreased embryo size	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620649	F	MP:0008525	decreased cranium height	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620649	F	MP:0000547	short limbs	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620649	F	MP:0000111	cleft palate	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620649	F	MP:0005380	embryo phenotype	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	Y	16311594
MGI:3620649	F	MP:0000150	abnormal rib morphology	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620650	M	MP:0001701	incomplete embryo turning	Ofd1<tm2.1Bfra>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620650	M	MP:0001706	abnormal left-right axis patterning	Ofd1<tm2.1Bfra>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620650	M	MP:0000292	distended pericardium	Ofd1<tm2.1Bfra>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620650	M	MP:0004252	abnormal direction of heart looping	Ofd1<tm2.1Bfra>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620650	M	MP:0000270	abnormal heart tube morphology	Ofd1<tm2.1Bfra>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620650	M	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Ofd1<tm2.1Bfra>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620650	M	MP:0009937	abnormal neuron differentiation	Ofd1<tm2.1Bfra>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620650	M	MP:0000926	absent floor plate	Ofd1<tm2.1Bfra>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620650	M	MP:0001698	decreased embryo size	Ofd1<tm2.1Bfra>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S2/SvPas	N	16311594
MGI:3620827	F	MP:0031420	decreased superovulation rate	Gja1<M1Jrt>/Gja1<+>	involves: C3H/HeJ * C57BL/6J	N	19259389
MGI:3620827	F	MP:0001126	abnormal ovary morphology	Gja1<M1Jrt>/Gja1<+>	involves: C3H/HeJ * C57BL/6J	N	19259389
MGI:3620827	F	MP:0001923	reduced female fertility	Gja1<M1Jrt>/Gja1<+>	involves: C3H/HeJ * C57BL/6J	N	19259389
MGI:3620827	F	MP:0013508	increased granulosa cell apoptosis	Gja1<M1Jrt>/Gja1<+>	involves: C3H/HeJ * C57BL/6J	N	19259389
MGI:3620827	F	MP:0031018	decreased granulosa cell proliferation	Gja1<M1Jrt>/Gja1<+>	involves: C3H/HeJ * C57BL/6J	N	19259389
MGI:3620827	F	MP:0008868	abnormal granulosa cell morphology	Gja1<M1Jrt>/Gja1<+>	involves: C3H/HeJ * C57BL/6J	N	19259389
MGI:3620827	F	MP:0002682	decreased mature ovarian follicle number	Gja1<M1Jrt>/Gja1<+>	involves: C3H/HeJ * C57BL/6J	N	19259389
MGI:3620827	F	MP:0001882	abnormal lactation	Gja1<M1Jrt>/Gja1<+>	involves: C3H/HeJ * C57BL/6J	N	19259389
MGI:3620841	F	MP:0001126	abnormal ovary morphology	Gja1<M1Jrt>/Gja1<+>	involves: C3H/HeJ * C57BL/6J * FVB/N	N	16155213
MGI:3620910	M	MP:0001153	small seminiferous tubules	Lmna<tm1Stw>/Lmna<tm1Stw>	involves: 129S1/Sv * C57BL/6	N	14996939
MGI:3620910	M	MP:0005159	azoospermia	Lmna<tm1Stw>/Lmna<tm1Stw>	involves: 129S1/Sv * C57BL/6	N	14996939
MGI:3620910	M	MP:0008261	arrest of male meiosis	Lmna<tm1Stw>/Lmna<tm1Stw>	involves: 129S1/Sv * C57BL/6	N	14996939
MGI:3620910	M	MP:0001147	small testis	Lmna<tm1Stw>/Lmna<tm1Stw>	involves: 129S1/Sv * C57BL/6	N	14996939
MGI:3620985	M	MP:0002216	abnormal seminiferous tubule morphology	Gja1<tm2(Gjb1)Kwi>/Gja1<tm2(Gjb1)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620985	M	MP:0004852	decreased testis weight	Gja1<tm2(Gjb1)Kwi>/Gja1<tm2(Gjb1)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620985	F	MP:0001923	reduced female fertility	Gja1<tm2(Gjb1)Kwi>/Gja1<tm2(Gjb1)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620985	F	MP:0001131	abnormal ovarian follicle morphology	Gja1<tm2(Gjb1)Kwi>/Gja1<tm2(Gjb1)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620985	F	MP:0003355	decreased ovulation rate	Gja1<tm2(Gjb1)Kwi>/Gja1<tm2(Gjb1)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620985	M	MP:0001925	male infertility	Gja1<tm2(Gjb1)Kwi>/Gja1<tm2(Gjb1)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620985	M	MP:0002687	oligozoospermia	Gja1<tm2(Gjb1)Kwi>/Gja1<tm2(Gjb1)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620991	F	MP:0013781	abnormal mammary gland luminal epithelium morphology	Gja1<tm2(Gjb1)Kwi>/Gja1<+>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620991	F	MP:0003838	abnormal milk ejection	Gja1<tm2(Gjb1)Kwi>/Gja1<+>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620991	F	MP:0009506	abnormal mammary gland alveolus morphology	Gja1<tm2(Gjb1)Kwi>/Gja1<+>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620992	M	MP:0002687	oligozoospermia	Gja1<tm3(Gja5)Kwi>/Gja1<tm3(Gja5)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620992	M	MP:0004852	decreased testis weight	Gja1<tm3(Gja5)Kwi>/Gja1<tm3(Gja5)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620992	F	MP:0001926	female infertility	Gja1<tm3(Gja5)Kwi>/Gja1<tm3(Gja5)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620992	F	MP:0003355	decreased ovulation rate	Gja1<tm3(Gja5)Kwi>/Gja1<tm3(Gja5)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620992	M	MP:0002216	abnormal seminiferous tubule morphology	Gja1<tm3(Gja5)Kwi>/Gja1<tm3(Gja5)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620992	F	MP:0001131	abnormal ovarian follicle morphology	Gja1<tm3(Gja5)Kwi>/Gja1<tm3(Gja5)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3620992	M	MP:0001925	male infertility	Gja1<tm3(Gja5)Kwi>/Gja1<tm3(Gja5)Kwi>	involves: 129P2/OlaHsd * C57BL/6	N	10996788
MGI:3621178	F	MP:0001923	reduced female fertility	Fancg<tm1Faw>/Fancg<tm1Faw>	involves: 129P2/OlaHsd * FVB/N	N	11823446
MGI:3621178	M	MP:0001147	small testis	Fancg<tm1Faw>/Fancg<tm1Faw>	involves: 129P2/OlaHsd * FVB/N	N	11823446
MGI:3621178	M	MP:0001922	reduced male fertility	Fancg<tm1Faw>/Fancg<tm1Faw>	involves: 129P2/OlaHsd * FVB/N	N	11823446
MGI:3621178	F	MP:0001126	abnormal ovary morphology	Fancg<tm1Faw>/Fancg<tm1Faw>	involves: 129P2/OlaHsd * FVB/N	N	11823446
MGI:3621178	F	MP:0001130	abnormal ovarian folliculogenesis	Fancg<tm1Faw>/Fancg<tm1Faw>	involves: 129P2/OlaHsd * FVB/N	N	11823446
MGI:3621178	M	MP:0002216	abnormal seminiferous tubule morphology	Fancg<tm1Faw>/Fancg<tm1Faw>	involves: 129P2/OlaHsd * FVB/N	N	11823446
MGI:3621178	M	MP:0001932	abnormal spermiogenesis	Fancg<tm1Faw>/Fancg<tm1Faw>	involves: 129P2/OlaHsd * FVB/N	N	11823446
MGI:3621178	F	MP:0001127	small ovary	Fancg<tm1Faw>/Fancg<tm1Faw>	involves: 129P2/OlaHsd * FVB/N	N	11823446
MGI:3621178	M	MP:0001152	increased Leydig cell number	Fancg<tm1Faw>/Fancg<tm1Faw>	involves: 129P2/OlaHsd * FVB/N	N	11823446
MGI:3621191	F	MP:0005168	abnormal female meiosis	Akap1<tm1Gsm>/Akap1<tm1Gsm>	B6.Cg-Akap1<tm1Gsm>	N	16461287
MGI:3621191	F	MP:0001923	reduced female fertility	Akap1<tm1Gsm>/Akap1<tm1Gsm>	B6.Cg-Akap1<tm1Gsm>	N	16461287
MGI:3621359	F	MP:0031434	increased miscarriage rate	S1pr3<tm1Rlp>/S1pr3<tm1Rlp>,S1pr2<tm1Rlp>/S1pr2<tm1Rlp>	involves: 129S6/SvEvTac * C57BL/6	N	15138255
MGI:3621365	M	MP:0004852	decreased testis weight	Fancg<tm1Ada>/Fancg<tm1Ada>	involves: 129S4/SvJae * C57BL/6	N	11719385
MGI:3621365	F	MP:0001130	abnormal ovarian folliculogenesis	Fancg<tm1Ada>/Fancg<tm1Ada>	involves: 129S4/SvJae * C57BL/6	N	11719385
MGI:3621365	F	MP:0001126	abnormal ovary morphology	Fancg<tm1Ada>/Fancg<tm1Ada>	involves: 129S4/SvJae * C57BL/6	N	11719385
MGI:3621365	M	MP:0001146	abnormal testis morphology	Fancg<tm1Ada>/Fancg<tm1Ada>	involves: 129S4/SvJae * C57BL/6	N	11719385
MGI:3621365	M	MP:0002216	abnormal seminiferous tubule morphology	Fancg<tm1Ada>/Fancg<tm1Ada>	involves: 129S4/SvJae * C57BL/6	N	11719385
MGI:3621365	F	MP:0001923	reduced female fertility	Fancg<tm1Ada>/Fancg<tm1Ada>	involves: 129S4/SvJae * C57BL/6	N	11719385
MGI:3621365	M	MP:0001922	reduced male fertility	Fancg<tm1Ada>/Fancg<tm1Ada>	involves: 129S4/SvJae * C57BL/6	N	11719385
MGI:3621375	F	MP:0005369	muscle phenotype	Emd<tm1.1Stw>/Emd<tm1.1Stw>	involves: 129S1/Sv * FVB/N	Y	16403804
MGI:3621375	F	MP:0005384	cellular phenotype	Emd<tm1.1Stw>/Emd<tm1.1Stw>	involves: 129S1/Sv * FVB/N	Y	16403804
MGI:3621419	M	MP:0005384	cellular phenotype	Emd<tm1.1Stw>/Y	involves: 129S1/Sv * FVB/N	Y	16403804
MGI:3621419	M	MP:0003082	abnormal gastrocnemius morphology	Emd<tm1.1Stw>/Y	involves: 129S1/Sv * FVB/N	N	16403804
MGI:3621424	F	MP:0001405	impaired coordination	Emd<tm1Ykh>/Emd<tm1Ykh>	B6.129X1-Emd<tm1Ykh>	N	16507906
MGI:3621424	F	MP:0000278	abnormal myocardial fiber morphology	Emd<tm1Ykh>/Emd<tm1Ykh>	B6.129X1-Emd<tm1Ykh>	N	16507906
MGI:3621424	F	MP:0003896	prolonged PR interval	Emd<tm1Ykh>/Emd<tm1Ykh>	B6.129X1-Emd<tm1Ykh>	N	16507906
MGI:3621424	F	MP:0003084	abnormal skeletal muscle fiber morphology	Emd<tm1Ykh>/Emd<tm1Ykh>	B6.129X1-Emd<tm1Ykh>	N	16507906
MGI:3621425	F	MP:0001405	impaired coordination	Emd<tm1Ykh>/Emd<+>	B6.129X1-Emd<tm1Ykh>	N	16507906
MGI:3621426	M	MP:0003084	abnormal skeletal muscle fiber morphology	Emd<tm1Ykh>/Y	B6.129X1-Emd<tm1Ykh>	N	16507906
MGI:3621426	M	MP:0000278	abnormal myocardial fiber morphology	Emd<tm1Ykh>/Y	B6.129X1-Emd<tm1Ykh>	N	16507906
MGI:3621426	M	MP:0001405	impaired coordination	Emd<tm1Ykh>/Y	B6.129X1-Emd<tm1Ykh>	N	16507906
MGI:3621426	M	MP:0003896	prolonged PR interval	Emd<tm1Ykh>/Y	B6.129X1-Emd<tm1Ykh>	N	16507906
MGI:3621428	M	MP:0002647	decreased intestinal cholesterol absorption	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0003975	increased circulating VLDL triglyceride level	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0031631	decreased lung cholesterol level	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0005365	abnormal bile salt homeostasis	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0000599	enlarged liver	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0013307	increased adrenal gland weight	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0002175	decreased brain weight	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0001552	increased circulating triglyceride level	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0003982	increased cholesterol level	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0005281	increased fatty acids level	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0005376	homeostasis/metabolism phenotype	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	Y	11001949
MGI:3621428	M	MP:0005178	increased circulating cholesterol level	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0012338	decreased bile salt level	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0000642	enlarged adrenal glands	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0003868	abnormal feces composition	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0000646	enlarged adrenocortical cells	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0002981	increased liver weight	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0009355	increased liver triglyceride level	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0005145	increased circulating VLDL cholesterol level	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0004773	abnormal bile composition	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0012226	increased sterol level	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621428	M	MP:0003918	decreased kidney weight	Cyp27a1<tm1Elt>/Cyp27a1<tm1Elt>	involves: 129/Sv * C57BL/6J	N	11001949
MGI:3621443	M	MP:0001922	reduced male fertility	Lrp8<tm4Her>/Lrp8<tm4Her>	Not Specified	N	16481437
MGI:3621460	M	MP:0001613	abnormal vasodilation	Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	N	15798202
MGI:3621460	M	MP:0001859	kidney inflammation	Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	N	16510575
MGI:3621460	M	MP:0002047	increased hepatic hemangioma incidence	Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	N	15798202
MGI:3621460	M	MP:0003675	kidney cyst	Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	N	16510575
MGI:3621460	M	MP:0002872	polycythemia	Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	N	15798202
MGI:3621460	M	MP:0005564	increased hemoglobin content	Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	N	15798202
MGI:3621460	M	MP:0000530	abnormal kidney vasculature morphology	Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	N	16510575
MGI:3621460	M	MP:0002135	abnormal kidney morphology	Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	N	16510575
MGI:3621460	M	MP:0006056	increased vascular endothelial cell number	Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	N	15798202
MGI:3621460	M	MP:0002628	hepatic steatosis	Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	N	15798202
MGI:3621461	M	MP:0000530	abnormal kidney vasculature morphology	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	N	16510575
MGI:3621461	M	MP:0002047	increased hepatic hemangioma incidence	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	N	15798202
MGI:3621461	M	MP:0001859	kidney inflammation	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	N	16510575
MGI:3621461	M	MP:0005564	increased hemoglobin content	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	N	15798202
MGI:3621461	M	MP:0002872	polycythemia	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	N	15798202
MGI:3621461	M	MP:0002135	abnormal kidney morphology	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	N	16510575
MGI:3621461	M	MP:0003675	kidney cyst	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	N	16510575
MGI:3621461	M	MP:0001613	abnormal vasodilation	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	N	15798202
MGI:3621461	M	MP:0006056	increased vascular endothelial cell number	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	N	15798202
MGI:3621461	M	MP:0002628	hepatic steatosis	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	N	15798202
MGI:3621462	M	MP:0005367	renal/urinary system phenotype	Arnt<tm1Bra>/Arnt<tm1Bra>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	Y	16510575
MGI:3621462	M	MP:0002628	hepatic steatosis	Arnt<tm1Bra>/Arnt<tm1Bra>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	N	15798202
MGI:3621462	M	MP:0002006	neoplasm	Arnt<tm1Bra>/Arnt<tm1Bra>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	Y	15798202
MGI:3621462	M	MP:0005397	hematopoietic system phenotype	Arnt<tm1Bra>/Arnt<tm1Bra>,Hprt1<tm1(Pck1-cre)Vhh>/Y,Vhl<tm1Jae>/Vhl<tm1Jae>	involves: 129 * BALB/c * C57BL/6	Y	15798202
MGI:3621491	F	MP:0011952	decreased cardiac stroke volume	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0020309	increased creatine kinase activity	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0008560	increased tumor necrosis factor secretion	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	19451692
MGI:3621491	F	MP:0003199	calcified muscle	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0008705	increased interleukin-6 secretion	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	19451692
MGI:3621491	F	MP:0009403	increased variability of skeletal muscle fiber size	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3621491	F	MP:0013237	abnormal skeletal muscle regeneration	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0010090	increased circulating creatine kinase level	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3621491	F	MP:0002841	impaired skeletal muscle contractility	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0001923	reduced female fertility	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3621491	F	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0000751	myopathy	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3621491	F	MP:0009461	skeletal muscle hypertrophy	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0002269	muscular atrophy	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3621491	F	MP:0000752	dystrophic muscle	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0000752	dystrophic muscle	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3621491	F	MP:0001515	abnormal grip strength	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	16540561
MGI:3621491	F	MP:0005385	cardiovascular system phenotype	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	Y	26566673
MGI:3621491	F	MP:0000749	muscle degeneration	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3621491	F	MP:0011966	abnormal auditory brainstem response waveform shape	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	12148865
MGI:3621491	F	MP:0009415	skeletal muscle degeneration	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0009419	skeletal muscle fibrosis	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3621491	F	MP:0005330	cardiomyopathy	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0011967	increased or absent threshold for auditory brainstem response	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	12148865
MGI:3621491	F	MP:0001405	impaired coordination	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	16540561
MGI:3621491	F	MP:0004597	increased susceptibility to noise-induced hearing loss	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	12148865
MGI:3621491	F	MP:0010106	abnormal circulating pyruvate kinase level	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3621491	F	MP:0003852	skeletal muscle necrosis	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3621491	F	MP:0008663	increased interleukin-12 secretion	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	19451692
MGI:3621491	F	MP:0008687	increased interleukin-2 secretion	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	19451692
MGI:3621491	F	MP:0008699	increased interleukin-4 secretion	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	19451692
MGI:3621491	F	MP:0010053	decreased grip strength	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0001264	increased body size	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0004818	increased skeletal muscle mass	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0004510	myositis	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0003393	decreased cardiac output	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0000274	enlarged heart	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0002106	abnormal muscle physiology	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	8433102
MGI:3621491	F	MP:0010090	increased circulating creatine kinase level	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3621491	F	MP:0008566	increased interferon-gamma secretion	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	19451692
MGI:3621491	F	MP:0005140	decreased cardiac muscle contractility	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0004089	dilated sarcoplasmic reticulum	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3621491	F	MP:0009401	increased skeletal muscle fiber diameter	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	26566673
MGI:3621491	F	MP:0002108	abnormal muscle morphology	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3621555	F	MP:0008779	abnormal maternal behavior	Nos1<tm1Plh>/Nos1<tm1Plh>	B6.129S4-Nos1<tm1Plh>	N	10479702
MGI:3621644	M	MP:0003795	abnormal bone structure	917M/917M<+>	C57BL/6-917M	N	15883645
MGI:3621644	M	MP:0010124	decreased bone mineral content	917M/917M<+>	C57BL/6-917M	N	15883645
MGI:3621644	M	MP:0030439	decreased osteoblast proliferation	917M/917M<+>	C57BL/6-917M	N	15883645
MGI:3621645	F	MP:0001923	reduced female fertility	Lcn2<tm1Mak>/Lcn2<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	N	16446425
MGI:3621737	F	MP:0009006	prolonged estrous cycle	Il5<tm1Kopf>/Il5<tm1Kopf>	either: C57BL/6-Il5<tm1Kopf> or (involves: BALB/c * C57BL/6) or (involves: C57BL/6 * CBA)	N	11058459
MGI:3621737	F	MP:0001376	abnormal mating receptivity	Il5<tm1Kopf>/Il5<tm1Kopf>	either: C57BL/6-Il5<tm1Kopf> or (involves: BALB/c * C57BL/6) or (involves: C57BL/6 * CBA)	N	11058459
MGI:3621771	M	MP:0003205	testicular atrophy	E2f1<tm1Meg>/E2f1<tm1Meg>	either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	N	8653790
MGI:3621817	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Ikbkg<tm1Mka>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621817	M	MP:0000598	abnormal liver morphology	Ikbkg<tm1Mka>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621817	M	MP:0003887	increased hepatocyte apoptosis	Ikbkg<tm1Mka>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0009580	increased keratinocyte apoptosis	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0008253	absent megakaryocytes	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0000745	tremors	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0001262	decreased body weight	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0003887	increased hepatocyte apoptosis	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0011086	postnatal lethality, incomplete penetrance	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0003454	erythroderma	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0002398	abnormal bone marrow cell morphology/development	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0000416	sparse hair	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0001392	abnormal locomotor behavior	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0008843	absent subcutaneous adipose tissue	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0003427	parakeratosis	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0001242	hyperkeratosis	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0000692	small spleen	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0000706	small thymus	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621818	F	MP:0006042	increased apoptosis	Ikbkg<tm1Mka>/Ikbkg<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10911991
MGI:3621910	F	MP:0012010	parturition failure	Pla2g4a<tm1Tksh>/Pla2g4a<tm1Tksh>	involves: 129P2/OlaHsd * C57BL/6J	N	9403692
MGI:3621972	M	MP:0001925	male infertility	Tpst2<tm1Klm>/Tpst2<tm1Klm>	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	16469738
MGI:3622099	M	MP:0001156	abnormal spermatogenesis	Spag16<tm2Jfs>/Spag16<+>	involves: 129S6/SvEvTac	N	16382026
MGI:3622100	M	MP:0001925	male infertility	Spag16<tm2Jfs>/Spag16<tm2Jfs>	involves: 129S6/SvEvTac	N	16382026
MGI:3622100	M	MP:0002675	asthenozoospermia	Spag16<tm2Jfs>/Spag16<tm2Jfs>	involves: 129S6/SvEvTac	N	16382026
MGI:3622100	M	MP:0005578	teratozoospermia	Spag16<tm2Jfs>/Spag16<tm2Jfs>	involves: 129S6/SvEvTac	N	16382026
MGI:3622100	M	MP:0001147	small testis	Spag16<tm2Jfs>/Spag16<tm2Jfs>	involves: 129S6/SvEvTac	N	16382026
MGI:3622104	M	MP:0005598	decreased heart ventricle muscle contractility	Hbegf<tm1Dcl>/Hbegf<tm1Dcl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12773386
MGI:3622110	M	MP:0005598	decreased heart ventricle muscle contractility	Btc<tm1Dcl>/Btc<tm1Dcl>,Hbegf<tm1Dcl>/Hbegf<tm1Dcl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12773386
MGI:3622114	F	MP:0001399	hyperactivity	Dkk3<tm1Cni>/Dkk3<tm1Cni>	involves: 129X1/SvJ * C57BL/6	N	16508007
MGI:3622114	F	MP:0008045	decreased NK cell number	Dkk3<tm1Cni>/Dkk3<tm1Cni>	involves: 129X1/SvJ * C57BL/6	N	16508007
MGI:3622116	F	MP:0004856	decreased ovary weight	Nos1<tm2Plh>/Nos1<tm2Plh>	Not Specified	N	12072412
MGI:3622116	M	MP:0004852	decreased testis weight	Nos1<tm2Plh>/Nos1<tm2Plh>	Not Specified	N	12072412
MGI:3622116	F	MP:0002680	decreased corpora lutea number	Nos1<tm2Plh>/Nos1<tm2Plh>	Not Specified	N	12072412
MGI:3622116	F	MP:0001923	reduced female fertility	Nos1<tm2Plh>/Nos1<tm2Plh>	Not Specified	N	12072412
MGI:3622116	M	MP:0001925	male infertility	Nos1<tm2Plh>/Nos1<tm2Plh>	Not Specified	N	12072412
MGI:3622122	M	MP:0011464	bilirubinuria	Abcc2<tm1Ahs>/Abcc2<tm1Ahs>	FVB.129P2-Abcc2<tm1Ahs>	N	22917771
MGI:3622122	M	MP:0005344	increased circulating bilirubin level	Abcc2<tm1Ahs>/Abcc2<tm1Ahs>	FVB.129P2-Abcc2<tm1Ahs>	N	22917771
MGI:3622152	F	MP:0001727	abnormal embryo implantation	Dnah11<iv>/Dnah11<iv>	SI/Col Tyrp1<b> Dnah11<iv>/J	N	1638728
MGI:3622153	F	MP:0001926	female infertility	Aaas<tm1Ahue>/Aaas<tm1Ahue>	involves: 129P2/OlaHsd * C57BL/6	N	16479006
MGI:3622167	M	MP:0005668	decreased circulating leptin level	Mchr1<tm1Yush>/Mchr1<tm1Yush>	involves: 129 * C57BL/6	N	12072376
MGI:3622167	M	MP:0005450	abnormal energy expenditure	Mchr1<tm1Yush>/Mchr1<tm1Yush>	involves: 129 * C57BL/6	N	12072376
MGI:3622188	M	MP:0004542	impaired acrosome reaction	Glra1<spd>/Glra1<+>	B6C3Fe a/a-Glra1<spd>/J	N	11076688
MGI:3622189	M	MP:0004542	impaired acrosome reaction	Glrb<spa>/Glrb<+>	B6C3Fe a/a-Glrb<spa>/J	N	11076688
MGI:3622281	M	MP:0001922	reduced male fertility	Vipr2<tm1Hmh>/Vipr2<tm1Hmh>	involves: 129P2/OlaHsd * C57BL/6	N	12239111
MGI:3622281	M	MP:0001154	seminiferous tubule degeneration	Vipr2<tm1Hmh>/Vipr2<tm1Hmh>	involves: 129P2/OlaHsd * C57BL/6	N	12239111
MGI:3622318	F	MP:0003356	impaired luteinization	Fzd4<tm1Nat>/Fzd4<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16093361
MGI:3622318	F	MP:0002679	abnormal corpus luteum morphology	Fzd4<tm1Nat>/Fzd4<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16093361
MGI:3622318	F	MP:0001134	absent corpus luteum	Fzd4<tm1Nat>/Fzd4<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16093361
MGI:3622318	M	MP:0001925	male infertility	Fzd4<tm1Nat>/Fzd4<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16093361
MGI:3622318	F	MP:0001926	female infertility	Fzd4<tm1Nat>/Fzd4<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16093361
MGI:3622318	F	MP:0001133	impaired luteal cell differentiation	Fzd4<tm1Nat>/Fzd4<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16093361
MGI:3622318	F	MP:0001728	failure of embryo implantation	Fzd4<tm1Nat>/Fzd4<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16093361
MGI:3622547	F	MP:0010249	lactation failure	Dgat1<tm1Far>/Dgat1<tm1Far>	involves: 129S4/SvJae * C57BL/6J	N	10802663
MGI:3622901	F	MP:0009021	absent estrus	Ptprs<tm1Mtr>/Ptprs<tm1Mtr>	involves: 129/Sv * BALB/c	N	10080191
MGI:3622901	F	MP:0009009	absent estrous cycle	Ptprs<tm1Mtr>/Ptprs<tm1Mtr>	involves: 129/Sv * BALB/c	N	10080191
MGI:3622910	M	MP:0001925	male infertility	Rara<tm3.1Ipc>/Rara<tm3.1Ipc>	involves: 129/Sv * C57BL/6 * SJL	N	11857786
MGI:3622910	M	MP:0001146	abnormal testis morphology	Rara<tm3.1Ipc>/Rara<tm3.1Ipc>	involves: 129/Sv * C57BL/6 * SJL	N	11857786
MGI:3623146	M	MP:0003638	abnormal response/metabolism to endogenous compounds	Grpr<tm1Wada>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	9345264
MGI:3623146	M	MP:0001360	abnormal social investigation	Grpr<tm1Wada>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	9345264
MGI:3623146	M	MP:0031391	increased locomotor activity	Grpr<tm1Wada>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	9345264
MGI:3623216	F	MP:0001926	female infertility	Scarb1<tm1Kri>/Scarb1<tm1Kri>	B6.129S2-Scarb1<tm1Kri>	N	11733567
MGI:3623258	F	MP:0001386	abnormal maternal nurturing	Nmbr<tm1Hoh>/Nmbr<tm1Hoh>	involves: 129P2/OlaHsd * C57BL/6J	N	12231437
MGI:3623281	F	MP:0000662	abnormal branching of the mammary ductal tree	Cbl<tm1Ddlb>/Cbl<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	N	9671496
MGI:3623313	F	MP:0001142	abnormal vagina orifice morphology	Egfr<wa2>/Egfr<Wa5>	involves: BALB/cAnN * C3H/HeN * C57BL/6J	N	15366372
MGI:3623394	M	MP:0002566	abnormal sexual interaction	Hnf1a<tm1.1Ylee>/Hnf1a<tm1.1Ylee>	involves: 129X1/SvJ * C57BL/6J	N	9566924
MGI:3623394	M	MP:0001156	abnormal spermatogenesis	Hnf1a<tm1.1Ylee>/Hnf1a<tm1.1Ylee>	involves: 129X1/SvJ * C57BL/6J	N	9566924
MGI:3623584	M	MP:0030780	increased urine glycerol level	Gk<tm1Wjc>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	9302256
MGI:3623584	M	MP:0003443	increased circulating glycerol level	Gk<tm1Wjc>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	9302256
MGI:3623584	M	MP:0001402	decreased locomotor activity	Gk<tm1Wjc>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16105550
MGI:3623584	M	MP:0001746	abnormal pituitary secretion	Gk<tm1Wjc>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	9302256
MGI:3623584	M	MP:0001436	abnormal suckling behavior	Gk<tm1Wjc>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	9302256
MGI:3623584	M	MP:0001436	abnormal suckling behavior	Gk<tm1Wjc>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16105550
MGI:3623584	M	MP:0011085	postnatal lethality, complete penetrance	Gk<tm1Wjc>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16105550
MGI:3623584	M	MP:0001732	postnatal growth retardation	Gk<tm1Wjc>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	9302256
MGI:3623584	M	MP:0002628	hepatic steatosis	Gk<tm1Wjc>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	9302256
MGI:3623584	M	MP:0000189	hypoglycemia	Gk<tm1Wjc>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	16105550
MGI:3623584	M	MP:0000189	hypoglycemia	Gk<tm1Wjc>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	9302256
MGI:3623584	M	MP:0011085	postnatal lethality, complete penetrance	Gk<tm1Wjc>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	9302256
MGI:3623584	M	MP:0005281	increased fatty acids level	Gk<tm1Wjc>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	9302256
MGI:3623586	F	MP:0006271	abnormal involution of the mammary gland	Mfge8<Gt(KST227)Byg>/Mfge8<Gt(KST227)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	16195353
MGI:3623586	F	MP:0009503	abnormal mammary gland duct morphology	Mfge8<Gt(KST227)Byg>/Mfge8<Gt(KST227)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	16195353
MGI:3623586	M	MP:0001922	reduced male fertility	Mfge8<Gt(KST227)Byg>/Mfge8<Gt(KST227)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	16195353
MGI:3623586	F	MP:0013148	mastitis	Mfge8<Gt(KST227)Byg>/Mfge8<Gt(KST227)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	16195353
MGI:3623728	F	MP:0001382	abnormal nursing	Lrp4<dan>/Lrp4<dan>	129S2/SvPas-Lrp4<dan>	N	16517118
MGI:3623729	F	MP:0001382	abnormal nursing	Lrp4<mdig>/Lrp4<mdig>	involves: 129S2/SvPas * DBA/1LacJ	N	16517118
MGI:3623749	F	MP:0001926	female infertility	Lep<ob>/Lep<ob>	B6.Cg-Lep<ob>/J	N	17550780
MGI:3623760	M	MP:0001454	abnormal cued conditioning behavior	Igbp1<tm1Imku>/Y,Tg(Igbp1b-cre)1Imku/0	B6.Cg-Igbp1<tm1Imku> Tg(Igbp1b-cre)1Imku	N	16516168
MGI:3623760	M	MP:0003631	nervous system phenotype	Igbp1<tm1Imku>/Y,Tg(Igbp1b-cre)1Imku/0	B6.Cg-Igbp1<tm1Imku> Tg(Igbp1b-cre)1Imku	Y	16516168
MGI:3623760	M	MP:0001463	abnormal spatial learning	Igbp1<tm1Imku>/Y,Tg(Igbp1b-cre)1Imku/0	B6.Cg-Igbp1<tm1Imku> Tg(Igbp1b-cre)1Imku	N	16516168
MGI:3623798	M	MP:0001925	male infertility	Lsr<tm1Mdar>/Lsr<tm1Mdar>	either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * MF1)	N	15265030
MGI:3624016	M	MP:0001925	male infertility	Tex14<tm1Zuk>/Tex14<tm1Zuk>	129S/SvEv-Tex14<tm1Zuk>	N	16549803
MGI:3624016	M	MP:0006379	abnormal spermatocyte morphology	Tex14<tm1Zuk>/Tex14<tm1Zuk>	129S/SvEv-Tex14<tm1Zuk>	N	16549803
MGI:3624016	M	MP:0004852	decreased testis weight	Tex14<tm1Zuk>/Tex14<tm1Zuk>	129S/SvEv-Tex14<tm1Zuk>	N	16549803
MGI:3624016	M	MP:0001147	small testis	Tex14<tm1Zuk>/Tex14<tm1Zuk>	129S/SvEv-Tex14<tm1Zuk>	N	16549803
MGI:3624016	M	MP:0002784	abnormal Sertoli cell morphology	Tex14<tm1Zuk>/Tex14<tm1Zuk>	129S/SvEv-Tex14<tm1Zuk>	N	16549803
MGI:3624016	M	MP:0008261	arrest of male meiosis	Tex14<tm1Zuk>/Tex14<tm1Zuk>	129S/SvEv-Tex14<tm1Zuk>	N	16549803
MGI:3624028	M	MP:0003915	increased heart left ventricle weight	Fkbp1b<tm1Syf>/Fkbp1b<tm1Syf>	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6)	N	11907581
MGI:3624028	M	MP:0006143	increased systemic arterial diastolic blood pressure	Fkbp1b<tm1Syf>/Fkbp1b<tm1Syf>	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6)	N	11907581
MGI:3624028	M	MP:0000231	hypertension	Fkbp1b<tm1Syf>/Fkbp1b<tm1Syf>	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6)	N	11907581
MGI:3624028	M	MP:0002833	increased heart weight	Fkbp1b<tm1Syf>/Fkbp1b<tm1Syf>	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6)	N	11907581
MGI:3624028	M	MP:0000281	abnormal interventricular septum morphology	Fkbp1b<tm1Syf>/Fkbp1b<tm1Syf>	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6)	N	11907581
MGI:3624028	M	MP:0010724	thick interventricular septum	Fkbp1b<tm1Syf>/Fkbp1b<tm1Syf>	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6)	N	11907581
MGI:3624028	M	MP:0006144	increased systemic arterial systolic blood pressure	Fkbp1b<tm1Syf>/Fkbp1b<tm1Syf>	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6)	N	11907581
MGI:3624028	M	MP:0021161	increased heart left ventricle posterior wall thickness	Fkbp1b<tm1Syf>/Fkbp1b<tm1Syf>	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6)	N	11907581
MGI:3624028	M	MP:0001625	cardiac hypertrophy	Fkbp1b<tm1Syf>/Fkbp1b<tm1Syf>	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6)	N	11907581
MGI:3624029	M	MP:0008261	arrest of male meiosis	Tex14<tm1Zuk>/Tex14<tm1Zuk>	either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J)	N	16549803
MGI:3624029	M	MP:0001156	abnormal spermatogenesis	Tex14<tm1Zuk>/Tex14<tm1Zuk>	either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J)	N	16549803
MGI:3624029	M	MP:0001147	small testis	Tex14<tm1Zuk>/Tex14<tm1Zuk>	either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J)	N	16549803
MGI:3624029	M	MP:0001925	male infertility	Tex14<tm1Zuk>/Tex14<tm1Zuk>	either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J)	N	16549803
MGI:3624321	M	MP:0001153	small seminiferous tubules	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	19258705
MGI:3624321	M	MP:0009232	abnormal sperm nucleus morphology	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	26306493
MGI:3624321	M	MP:0014052	increased male germ cell apoptosis	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	19258705
MGI:3624321	M	MP:0002675	asthenozoospermia	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	19258705
MGI:3624321	M	MP:0002687	oligozoospermia	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	19258705
MGI:3624321	M	MP:0001932	abnormal spermiogenesis	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	19258705
MGI:3624321	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	19258705
MGI:3624321	M	MP:0009232	abnormal sperm nucleus morphology	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	19258705
MGI:3624321	M	MP:0008898	abnormal acrosome morphology	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	26306493
MGI:3624321	M	MP:0005578	teratozoospermia	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	19258705
MGI:3624321	M	MP:0002686	globozoospermia	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	19258705
MGI:3624321	M	MP:0004852	decreased testis weight	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	19258705
MGI:3624321	M	MP:0001147	small testis	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	19258705
MGI:3624321	M	MP:0008898	abnormal acrosome morphology	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	19258705
MGI:3624321	M	MP:0001925	male infertility	Pick1<tm1Rlh>/Pick1<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ	N	19258705
MGI:3624431	M	MP:0001823	thymus hypoplasia	Il2rg<tm1Wjl>/Y,Crlf2<tm1Wjl>/Crlf2<tm1Wjl>	involves: 129S4/SvJae * C57BL/6	N	15263024
MGI:3624437	M	MP:0005536	decreased Leydig cell number	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	M	MP:0005159	azoospermia	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	F	MP:0001119	abnormal female reproductive system morphology	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	M	MP:0004852	decreased testis weight	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	M	MP:0008261	arrest of male meiosis	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	F	MP:0000627	abnormal mammary gland morphology	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	M	MP:0001153	small seminiferous tubules	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	F	MP:0004833	ovary atrophy	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	F	MP:0004895	vagina atrophy	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	M	MP:0001145	abnormal male reproductive system morphology	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	F	MP:0001134	absent corpus luteum	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	M	MP:0003205	testicular atrophy	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	F	MP:0001129	impaired ovarian folliculogenesis	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	M	MP:0002216	abnormal seminiferous tubule morphology	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	F	MP:0004894	uterus atrophy	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624437	F	MP:0004856	decreased ovary weight	Prokr2<tm1Api>/Prokr2<tm1Api>	involves: C57BL/6 * CBA	N	16537498
MGI:3624438	F	MP:0001923	reduced female fertility	Pomgnt1<Gt(OST179231)Lex>/Pomgnt1<Gt(OST179231)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	16458488
MGI:3624438	M	MP:0001925	male infertility	Pomgnt1<Gt(OST179231)Lex>/Pomgnt1<Gt(OST179231)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	16458488
MGI:3624447	M	MP:0013592	small thymus cortex	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0002723	abnormal immune serum protein physiology	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	15263024
MGI:3624447	M	MP:0002464	abnormal basophil physiology	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0008688	decreased interleukin-2 secretion	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0003850	abnormal thymocyte activation	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0002460	decreased immunoglobulin level	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0002722	abnormal immune system organ morphology	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	15263024
MGI:3624447	M	MP:0002458	abnormal B cell number	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	15263024
MGI:3624447	M	MP:0008046	absent NK cells	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0002423	abnormal mast cell physiology	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	15263024
MGI:3624447	M	MP:0002421	abnormal cell-mediated immunity	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	15263024
MGI:3624447	M	MP:0002619	abnormal lymphocyte morphology	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	15263024
MGI:3624447	M	MP:0009481	cecum inflammation	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0008700	decreased interleukin-4 secretion	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0000693	spleen hyperplasia	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0000706	small thymus	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0000694	spleen hypoplasia	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0005232	abnormal mesenteric lymph node morphology	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0005070	impaired natural killer cell mediated cytotoxicity	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0008567	decreased interferon-gamma secretion	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0000708	thymus hyperplasia	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	15263024
MGI:3624447	M	MP:0008352	absent gamma-delta intraepithelial T cell	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0008348	absent gamma-delta T cells	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0002217	small lymph nodes	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0008083	decreased single-positive T cell number	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0000494	abnormal cecum morphology	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0002378	abnormal gut-associated lymphoid tissue morphology	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0005092	decreased double-positive T cell number	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0005089	decreased double-negative T cell number	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0005095	decreased T cell proliferation	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624447	M	MP:0008215	decreased immature B cell number	Il2rg<tm1Wjl>/Y	involves: 129S4/SvJae * C57BL/6	N	7697543
MGI:3624527	M	MP:0005386	behavior/neurological phenotype	Tor1a<tm2Wtd>/Tor1a<+>	involves: 129S1/Sv	Y	22393392
MGI:3624551	M	MP:0001392	abnormal locomotor behavior	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0001408	stereotypic behavior	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0001360	abnormal social investigation	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0000745	tremors	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0001363	increased anxiety-related response	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0003849	greasy coat	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0001511	disheveled coat	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0001405	impaired coordination	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0002064	seizures	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0000160	kyphosis	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0002083	premature death	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0002757	decreased vertical activity	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0003111	abnormal cell nucleus morphology	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0001402	decreased locomotor activity	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624551	M	MP:0002066	abnormal motor capabilities/coordination/movement	Mecp2<tm1Hzo>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	12160743
MGI:3624553	M	MP:0001409	increased stereotypic behavior	Mecp2<tm1Hzo>/Y	129S7/SvEvBrd-Mecp2<tm1Hzo>	N	12160743
MGI:3624553	M	MP:0000745	tremors	Mecp2<tm1Hzo>/Y	129S7/SvEvBrd-Mecp2<tm1Hzo>	N	12160743
MGI:3624553	M	MP:0001405	impaired coordination	Mecp2<tm1Hzo>/Y	129S7/SvEvBrd-Mecp2<tm1Hzo>	N	12160743
MGI:3624554	F	MP:0000745	tremors	Mecp2<tm1Hzo>/Mecp2<+>	129S7/SvEvBrd-Mecp2<tm1Hzo>	N	12160743
MGI:3624554	F	MP:0004924	abnormal behavior	Mecp2<tm1Hzo>/Mecp2<+>	129S7/SvEvBrd-Mecp2<tm1Hzo>	N	12160743
MGI:3624554	F	MP:0001409	increased stereotypic behavior	Mecp2<tm1Hzo>/Mecp2<+>	129S7/SvEvBrd-Mecp2<tm1Hzo>	N	12160743
MGI:3624554	F	MP:0001405	impaired coordination	Mecp2<tm1Hzo>/Mecp2<+>	129S7/SvEvBrd-Mecp2<tm1Hzo>	N	12160743
MGI:3624674	M	MP:0005150	cachexia	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624674	M	MP:0001402	decreased locomotor activity	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624674	M	MP:0002083	premature death	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624674	M	MP:0008265	abnormal hippocampus CA2 region morphology	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624674	M	MP:0002882	abnormal neuron morphology	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624674	M	MP:0001492	abnormal pilomotor reflex	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624674	M	MP:0002175	decreased brain weight	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624674	M	MP:0000774	decreased brain size	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624674	M	MP:0000745	tremors	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624674	M	MP:0005535	abnormal body temperature	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624674	M	MP:0001943	abnormal respiration	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624674	M	MP:0001261	obese	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624674	M	MP:0004924	abnormal behavior	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624676	F	MP:0001957	apnea	Mecp2<tm1.1Jae>/Mecp2<+>	involves: 129S4/SvJae * BALB/c * C57BL/6	N	22302819
MGI:3624676	F	MP:0005426	tachypnea	Mecp2<tm1.1Jae>/Mecp2<+>	involves: 129S4/SvJae * BALB/c * C57BL/6	N	22302819
MGI:3624676	F	MP:0003212	increased susceptibility to age related obesity	Mecp2<tm1.1Jae>/Mecp2<+>	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624676	F	MP:0001951	abnormal breathing pattern	Mecp2<tm1.1Jae>/Mecp2<+>	involves: 129S4/SvJae * BALB/c * C57BL/6	N	22302819
MGI:3624676	F	MP:0001393	ataxia	Mecp2<tm1.1Jae>/Mecp2<+>	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624676	F	MP:0001402	decreased locomotor activity	Mecp2<tm1.1Jae>/Mecp2<+>	involves: 129S4/SvJae * BALB/c * C57BL/6	N	11242118
MGI:3624680	M	MP:0001402	decreased locomotor activity	Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624680	M	MP:0002175	decreased brain weight	Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624680	M	MP:0002882	abnormal neuron morphology	Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624680	M	MP:0001261	obese	Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624680	M	MP:0004924	abnormal behavior	Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624680	M	MP:0001943	abnormal respiration	Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624680	M	MP:0001492	abnormal pilomotor reflex	Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624680	M	MP:0008265	abnormal hippocampus CA2 region morphology	Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624680	M	MP:0000774	decreased brain size	Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624680	M	MP:0002083	premature death	Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624680	M	MP:0000745	tremors	Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624680	M	MP:0005150	cachexia	Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624684	F	MP:0001393	ataxia	Mecp2<tm1Jae>/Mecp2<+>,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624684	F	MP:0001402	decreased locomotor activity	Mecp2<tm1Jae>/Mecp2<+>,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624684	F	MP:0003212	increased susceptibility to age related obesity	Mecp2<tm1Jae>/Mecp2<+>,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	11242118
MGI:3624685	M	MP:0001402	decreased locomotor activity	Mecp2<tm1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * CBA/J	N	11242118
MGI:3624685	M	MP:0003212	increased susceptibility to age related obesity	Mecp2<tm1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * CBA/J	N	11242118
MGI:3624685	M	MP:0002175	decreased brain weight	Mecp2<tm1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * CBA/J	N	11242118
MGI:3624685	M	MP:0002882	abnormal neuron morphology	Mecp2<tm1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * CBA/J	N	11242118
MGI:3624685	M	MP:0001393	ataxia	Mecp2<tm1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * CBA/J	N	11242118
MGI:3624685	M	MP:0008265	abnormal hippocampus CA2 region morphology	Mecp2<tm1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * CBA/J	N	11242118
MGI:3624713	M	MP:0000454	abnormal jaw morphology	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624713	M	MP:0010070	decreased serotonin level	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	20633611
MGI:3624713	M	MP:0001407	short stride length	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	20633611
MGI:3624713	M	MP:0001406	abnormal gait	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	20633611
MGI:3624713	M	MP:0003313	abnormal locomotor activation	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	20633611
MGI:3624713	M	MP:0002204	abnormal synaptic neurotransmitter level	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	20633611
MGI:3624713	M	MP:0001260	increased body weight	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624713	M	MP:0001393	ataxia	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	20633611
MGI:3624713	M	MP:0001513	limb grasping	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624713	M	MP:0001951	abnormal breathing pattern	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624713	M	MP:0001402	decreased locomotor activity	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624713	M	MP:0002286	cryptorchism	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624713	M	MP:0002100	abnormal tooth morphology	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624713	M	MP:0002083	premature death	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624713	M	MP:0003312	abnormal locomotor coordination	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	20633611
MGI:3624713	M	MP:0012574	decreased noradrenaline level	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	20633611
MGI:3624713	M	MP:0001963	abnormal hearing physiology	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624713	M	MP:0001263	weight loss	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624713	M	MP:0001262	decreased body weight	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624713	M	MP:0001406	abnormal gait	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624717	F	MP:0001263	weight loss	Mecp2<tm1.1Bird>/Mecp2<tm1.1Bird>	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624717	F	MP:0001951	abnormal breathing pattern	Mecp2<tm1.1Bird>/Mecp2<tm1.1Bird>	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624717	F	MP:0001963	abnormal hearing physiology	Mecp2<tm1.1Bird>/Mecp2<tm1.1Bird>	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624717	F	MP:0001402	decreased locomotor activity	Mecp2<tm1.1Bird>/Mecp2<tm1.1Bird>	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624717	F	MP:0002083	premature death	Mecp2<tm1.1Bird>/Mecp2<tm1.1Bird>	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624717	F	MP:0002100	abnormal tooth morphology	Mecp2<tm1.1Bird>/Mecp2<tm1.1Bird>	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624717	F	MP:0001513	limb grasping	Mecp2<tm1.1Bird>/Mecp2<tm1.1Bird>	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624717	F	MP:0000454	abnormal jaw morphology	Mecp2<tm1.1Bird>/Mecp2<tm1.1Bird>	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624717	F	MP:0001406	abnormal gait	Mecp2<tm1.1Bird>/Mecp2<tm1.1Bird>	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624718	F	MP:0001513	limb grasping	Mecp2<tm1.1Bird>/Mecp2<+>	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624718	F	MP:0001402	decreased locomotor activity	Mecp2<tm1.1Bird>/Mecp2<+>	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624718	F	MP:0001951	abnormal breathing pattern	Mecp2<tm1.1Bird>/Mecp2<+>	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624719	M	MP:0001262	decreased body weight	Mecp2<tm1Bird>/Y,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	11242117
MGI:3624719	M	MP:0001402	decreased locomotor activity	Mecp2<tm1Bird>/Y,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	11242117
MGI:3624719	M	MP:0002286	cryptorchism	Mecp2<tm1Bird>/Y,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	11242117
MGI:3624719	M	MP:0001513	limb grasping	Mecp2<tm1Bird>/Y,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	11242117
MGI:3624719	M	MP:0002100	abnormal tooth morphology	Mecp2<tm1Bird>/Y,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	11242117
MGI:3624719	M	MP:0002083	premature death	Mecp2<tm1Bird>/Y,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	11242117
MGI:3624719	M	MP:0001406	abnormal gait	Mecp2<tm1Bird>/Y,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	11242117
MGI:3624722	M	MP:0002083	premature death	Mbd2<tm1Bh>/Mbd2<tm1Bh>,Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624722	M	MP:0002066	abnormal motor capabilities/coordination/movement	Mbd2<tm1Bh>/Mbd2<tm1Bh>,Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	11242117
MGI:3624725	F	MP:0001130	abnormal ovarian folliculogenesis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad4<tm1Rob>/Smad4<tm1.1Rob>	involves: 129S/SvEv * C57BL/6J	N	16513794
MGI:3624725	F	MP:0003355	decreased ovulation rate	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad4<tm1Rob>/Smad4<tm1.1Rob>	involves: 129S/SvEv * C57BL/6J	N	16513794
MGI:3624725	F	MP:0001131	abnormal ovarian follicle morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad4<tm1Rob>/Smad4<tm1.1Rob>	involves: 129S/SvEv * C57BL/6J	N	16513794
MGI:3624725	F	MP:0005431	decreased oocyte number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad4<tm1Rob>/Smad4<tm1.1Rob>	involves: 129S/SvEv * C57BL/6J	N	16513794
MGI:3624725	F	MP:0011129	decreased tertiary ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad4<tm1Rob>/Smad4<tm1.1Rob>	involves: 129S/SvEv * C57BL/6J	N	16513794
MGI:3624725	F	MP:0009374	absent cumulus expansion	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad4<tm1Rob>/Smad4<tm1.1Rob>	involves: 129S/SvEv * C57BL/6J	N	16513794
MGI:3624725	F	MP:0021106	abnormal secondary ovarian follicle morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad4<tm1Rob>/Smad4<tm1.1Rob>	involves: 129S/SvEv * C57BL/6J	N	16513794
MGI:3624725	F	MP:0031383	increased secondary ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad4<tm1Rob>/Smad4<tm1.1Rob>	involves: 129S/SvEv * C57BL/6J	N	16513794
MGI:3624725	F	MP:0008868	abnormal granulosa cell morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad4<tm1Rob>/Smad4<tm1.1Rob>	involves: 129S/SvEv * C57BL/6J	N	16513794
MGI:3624725	F	MP:0009373	abnormal cumulus expansion	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad4<tm1Rob>/Smad4<tm1.1Rob>	involves: 129S/SvEv * C57BL/6J	N	16513794
MGI:3624745	M	MP:0014185	cerebellum atrophy	L1cam<tm1(tTA)Msch>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624745	M	MP:0001265	decreased body size	L1cam<tm1(tTA)Msch>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624745	M	MP:0006254	thin cerebral cortex	L1cam<tm1(tTA)Msch>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624745	M	MP:0005537	abnormal cerebral aqueduct morphology	L1cam<tm1(tTA)Msch>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624745	M	MP:0000807	abnormal hippocampus morphology	L1cam<tm1(tTA)Msch>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624745	M	MP:0000822	abnormal brain ventricle morphology	L1cam<tm1(tTA)Msch>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624745	M	MP:0001891	hydrocephaly	L1cam<tm1(tTA)Msch>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624745	M	MP:0000439	enlarged cranium	L1cam<tm1(tTA)Msch>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624746	M	MP:0001891	hydrocephaly	L1cam<tm1Mtei>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624746	M	MP:0000807	abnormal hippocampus morphology	L1cam<tm1Mtei>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624746	M	MP:0006254	thin cerebral cortex	L1cam<tm1Mtei>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624746	M	MP:0001265	decreased body size	L1cam<tm1Mtei>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624746	M	MP:0000439	enlarged cranium	L1cam<tm1Mtei>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624746	M	MP:0014185	cerebellum atrophy	L1cam<tm1Mtei>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624746	M	MP:0005537	abnormal cerebral aqueduct morphology	L1cam<tm1Mtei>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624746	M	MP:0011380	enlarged brain ventricles	L1cam<tm1Mtei>/Y	involves: 129 * C57BL/6J	N	11164829
MGI:3624801	M	MP:0005316	abnormal response to tactile stimuli	L1cam<tm1Mtei>/Y	either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)	N	9354804
MGI:3624801	M	MP:0002733	abnormal thermal nociception	L1cam<tm1Mtei>/Y	either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)	N	9354804
MGI:3624801	M	MP:0001524	impaired limb coordination	L1cam<tm1Mtei>/Y	either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)	N	9354804
MGI:3624801	M	MP:0006198	enophthalmos	L1cam<tm1Mtei>/Y	either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)	N	9354804
MGI:3624801	M	MP:0011380	enlarged brain ventricles	L1cam<tm1Mtei>/Y	either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)	N	9354804
MGI:3624801	M	MP:0012484	decreased corticospinal tract size	L1cam<tm1Mtei>/Y	either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)	N	9354804
MGI:3624801	M	MP:0002882	abnormal neuron morphology	L1cam<tm1Mtei>/Y	either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)	N	9354804
MGI:3624801	M	MP:0001106	abnormal Schwann cell morphology	L1cam<tm1Mtei>/Y	either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)	N	9354804
MGI:3624801	M	MP:0002066	abnormal motor capabilities/coordination/movement	L1cam<tm1Mtei>/Y	either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)	N	9354804
MGI:3624801	M	MP:0010053	decreased grip strength	L1cam<tm1Mtei>/Y	either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)	N	9354804
MGI:3624801	M	MP:0001265	decreased body size	L1cam<tm1Mtei>/Y	either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)	N	9354804
MGI:3624851	M	MP:0004101	abnormal brain interneuron morphology	Dcx<tm1.2Ffr>/Y	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	16571605
MGI:3624851	M	MP:0004279	abnormal rostral migratory stream morphology	Dcx<tm1.2Ffr>/Y	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	16571605
MGI:3624868	F	MP:0001382	abnormal nursing	Cacna1a<tg-rol>/Cacna1a<tg-rol>	involves: C57BL/6 * SIII	N	4799944
MGI:3624868	F	MP:0001923	reduced female fertility	Cacna1a<tg-rol>/Cacna1a<tg-rol>	involves: C57BL/6 * SIII	N	4799944
MGI:3624868	M	MP:0001922	reduced male fertility	Cacna1a<tg-rol>/Cacna1a<tg-rol>	involves: C57BL/6 * SIII	N	4799944
MGI:3624942	M	MP:0002083	premature death	X/Yaa	(NZB x BXSB)F1	N	315777
MGI:3624942	M	MP:0002875	decreased erythrocyte cell number	X/Yaa	(NZB x BXSB)F1	N	315777
MGI:3624942	M	MP:0004797	increased anti-erythrocyte antigen antibody level	X/Yaa	(NZB x BXSB)F1	N	315777
MGI:3624942	M	MP:0004952	increased spleen weight	X/Yaa	(NZB x BXSB)F1	N	315777
MGI:3624942	M	MP:0001819	abnormal immune cell physiology	X/Yaa	(NZB x BXSB)F1	N	315777
MGI:3624942	M	MP:0005654	porphyria	X/Yaa	(NZB x BXSB)F1	N	315777
MGI:3624942	M	MP:0004794	increased anti-nuclear antigen antibody level	X/Yaa	(NZB x BXSB)F1	N	315777
MGI:3624942	M	MP:0005350	increased susceptibility to autoimmune disorder	X/Yaa	(NZB x BXSB)F1	N	315777
MGI:3624942	M	MP:0003725	increased autoantibody level	X/Yaa	(NZB x BXSB)F1	N	315777
MGI:3624942	M	MP:0002339	abnormal lymph node morphology	X/Yaa	(NZB x BXSB)F1	N	315777
MGI:3624942	M	MP:0000702	enlarged lymph nodes	X/Yaa	(NZB x BXSB)F1	N	315777
MGI:3624943	M	MP:0000702	enlarged lymph nodes	X/Yaa	(SJL/J x BXSB)F1	N	315777
MGI:3624943	M	MP:0005350	increased susceptibility to autoimmune disorder	X/Yaa	(SJL/J x BXSB)F1	N	315777
MGI:3624943	M	MP:0002083	premature death	X/Yaa	(SJL/J x BXSB)F1	N	315777
MGI:3624944	M	MP:0000702	enlarged lymph nodes	X/Yaa	(C57BL/6J x BXSB)F1	N	315777
MGI:3624944	M	MP:0002083	premature death	X/Yaa	(C57BL/6J x BXSB)F1	N	315777
MGI:3624944	M	MP:0005350	increased susceptibility to autoimmune disorder	X/Yaa	(C57BL/6J x BXSB)F1	N	315777
MGI:3624970	M	MP:0002083	premature death	X/Yaa	involves: BXSB * NZB	N	315777
MGI:3624970	M	MP:0005350	increased susceptibility to autoimmune disorder	X/Yaa	involves: BXSB * NZB	N	315777
MGI:3624970	M	MP:0000702	enlarged lymph nodes	X/Yaa	involves: BXSB * NZB	N	315777
MGI:3624973	M	MP:0002083	premature death	X/Yaa	BXSB/MpJ	N	315777
MGI:3624973	M	MP:0000702	enlarged lymph nodes	X/Yaa	BXSB/MpJ	N	315777
MGI:3624973	M	MP:0008502	increased IgG3 level	X/Yaa	BXSB/MpJ	N	15494482
MGI:3624973	M	MP:0004797	increased anti-erythrocyte antigen antibody level	X/Yaa	BXSB/MpJ	N	315777
MGI:3624973	M	MP:0009338	increased splenocyte number	X/Yaa	BXSB/MpJ	N	21964024
MGI:3624973	M	MP:0008470	abnormal spleen B cell follicle morphology	X/Yaa	BXSB/MpJ	N	21964024
MGI:3624973	M	MP:0005350	increased susceptibility to autoimmune disorder	X/Yaa	BXSB/MpJ	N	315777
MGI:3624973	M	MP:0004794	increased anti-nuclear antigen antibody level	X/Yaa	BXSB/MpJ	N	21964024
MGI:3624973	M	MP:0000220	increased monocyte cell number	X/Yaa	BXSB/MpJ	N	6363600
MGI:3624973	M	MP:0020519	renal glomerular immunoglobulin deposits	X/Yaa	BXSB/MpJ	N	21964024
MGI:3624973	M	MP:0003944	abnormal T cell subpopulation ratio	X/Yaa	BXSB/MpJ	N	21964024
MGI:3624973	M	MP:0008097	increased plasma cell number	X/Yaa	BXSB/MpJ	N	762500
MGI:3624973	M	MP:0002962	increased urine protein level	X/Yaa	BXSB/MpJ	N	6363600
MGI:3624973	M	MP:0002144	abnormal B cell differentiation	X/Yaa	BXSB/MpJ	N	762500
MGI:3624973	M	MP:0002083	premature death	X/Yaa	BXSB/MpJ	N	6363600
MGI:3624973	M	MP:0002743	glomerulonephritis	X/Yaa	BXSB/MpJ	N	315777
MGI:3624973	M	MP:0005350	increased susceptibility to autoimmune disorder	X/Yaa	BXSB/MpJ	N	762500
MGI:3624973	M	MP:0008499	increased IgG1 level	X/Yaa	BXSB/MpJ	N	15494482
MGI:3624973	M	MP:0002875	decreased erythrocyte cell number	X/Yaa	BXSB/MpJ	N	315777
MGI:3624973	M	MP:0008499	increased IgG1 level	X/Yaa	BXSB/MpJ	N	21964024
MGI:3624973	M	MP:0008500	increased IgG2a level	X/Yaa	BXSB/MpJ	N	21964024
MGI:3624973	M	MP:0002339	abnormal lymph node morphology	X/Yaa	BXSB/MpJ	N	315777
MGI:3624973	M	MP:0008501	increased IgG2b level	X/Yaa	BXSB/MpJ	N	21964024
MGI:3624973	M	MP:0009060	increased circulating interleukin-21 level	X/Yaa	BXSB/MpJ	N	15494482
MGI:3624973	M	MP:0004952	increased spleen weight	X/Yaa	BXSB/MpJ	N	315777
MGI:3624974	M	MP:0005350	increased susceptibility to autoimmune disorder	X/Yaa	(NZW x SB)F1	N	6690614
MGI:3624974	M	MP:0002723	abnormal immune serum protein physiology	X/Yaa	(NZW x SB)F1	N	6690614
MGI:3624974	M	MP:0002083	premature death	X/Yaa	(NZW x SB)F1	N	6690614
MGI:3624974	M	MP:0002743	glomerulonephritis	X/Yaa	(NZW x SB)F1	N	6690614
MGI:3624975	M	MP:0002723	abnormal immune serum protein physiology	X/Yaa	(NZW x BXSB)F1	N	6690614
MGI:3624975	M	MP:0002083	premature death	X/Yaa	(NZW x BXSB)F1	N	6690614
MGI:3624975	M	MP:0005350	increased susceptibility to autoimmune disorder	X/Yaa	(NZW x BXSB)F1	N	6690614
MGI:3624981	M	MP:0005385	cardiovascular system phenotype	ll/ll,X/Yaa	BXSB/MpJScr-ll	Y	1991974
MGI:3624981	M	MP:0001805	decreased IgG level	ll/ll,X/Yaa	BXSB/MpJScr-ll	N	1991974
MGI:3624981	M	MP:0004795	decreased anti-nuclear antigen antibody level	ll/ll,X/Yaa	BXSB/MpJScr-ll	N	1991974
MGI:3624981	M	MP:0002620	abnormal monocyte morphology	ll/ll,X/Yaa	BXSB/MpJScr-ll	N	1991974
MGI:3624981	M	MP:0012431	increased lymphoma incidence	ll/ll,X/Yaa	BXSB/MpJScr-ll	N	1991974
MGI:3624981	M	MP:0005367	renal/urinary system phenotype	ll/ll,X/Yaa	BXSB/MpJScr-ll	Y	1991974
MGI:3624981	M	MP:0002024	increased T cell derived lymphoma incidence	ll/ll,X/Yaa	BXSB/MpJScr-ll	N	1991974
MGI:3624981	M	MP:0008075	decreased CD4-positive, alpha-beta T cell number	ll/ll,X/Yaa	BXSB/MpJScr-ll	N	1991974
MGI:3624981	M	MP:0001661	extended life span	ll/ll,X/Yaa	BXSB/MpJScr-ll	N	1991974
MGI:3624981	M	MP:0005351	decreased susceptibility to autoimmune disorder	ll/ll,X/Yaa	BXSB/MpJScr-ll	N	1991974
MGI:3624982	M	MP:0004794	increased anti-nuclear antigen antibody level	X/Yaa	BXSB/MpJScr	N	1991974
MGI:3624982	M	MP:0002743	glomerulonephritis	X/Yaa	BXSB/MpJScr	N	1991974
MGI:3624982	M	MP:0000220	increased monocyte cell number	X/Yaa	BXSB/MpJScr	N	1991974
MGI:3624982	M	MP:0002083	premature death	X/Yaa	BXSB/MpJScr	N	1991974
MGI:3624982	M	MP:0005350	increased susceptibility to autoimmune disorder	X/Yaa	BXSB/MpJScr	N	1991974
MGI:3624982	M	MP:0002493	increased IgG level	X/Yaa	BXSB/MpJScr	N	1991974
MGI:3624982	M	MP:0008075	decreased CD4-positive, alpha-beta T cell number	X/Yaa	BXSB/MpJScr	N	1991974
MGI:3624989	M	MP:0001925	male infertility	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	involves: 129P2/OlaHsd * C57BL/6	N	16292313
MGI:3624989	F	MP:0005431	decreased oocyte number	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	involves: 129P2/OlaHsd * C57BL/6	N	16292313
MGI:3624989	F	MP:0001130	abnormal ovarian folliculogenesis	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	involves: 129P2/OlaHsd * C57BL/6	N	16292313
MGI:3624989	F	MP:0001926	female infertility	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	involves: 129P2/OlaHsd * C57BL/6	N	16292313
MGI:3624989	M	MP:0005159	azoospermia	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	involves: 129P2/OlaHsd * C57BL/6	N	16292313
MGI:3624989	F	MP:0005168	abnormal female meiosis	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	involves: 129P2/OlaHsd * C57BL/6	N	16292313
MGI:3624989	M	MP:0008261	arrest of male meiosis	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	involves: 129P2/OlaHsd * C57BL/6	N	16292313
MGI:3624989	M	MP:0004852	decreased testis weight	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	involves: 129P2/OlaHsd * C57BL/6	N	16292313
MGI:3625015	F	MP:0009503	abnormal mammary gland duct morphology	Gpat4<Gt(DTM030)Byg>/Gpat4<Gt(DTM030)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	16449762
MGI:3625015	F	MP:0009506	abnormal mammary gland alveolus morphology	Gpat4<Gt(DTM030)Byg>/Gpat4<Gt(DTM030)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	16449762
MGI:3625015	F	MP:0004047	abnormal milk composition	Gpat4<Gt(DTM030)Byg>/Gpat4<Gt(DTM030)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	16449762
MGI:3625015	F	MP:0000627	abnormal mammary gland morphology	Gpat4<Gt(DTM030)Byg>/Gpat4<Gt(DTM030)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	16449762
MGI:3625015	F	MP:0013716	hypolactation	Gpat4<Gt(DTM030)Byg>/Gpat4<Gt(DTM030)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	16449762
MGI:3625015	F	MP:0009504	abnormal mammary gland epithelium morphology	Gpat4<Gt(DTM030)Byg>/Gpat4<Gt(DTM030)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	16449762
MGI:3625081	F	MP:0005168	abnormal female meiosis	Stra8<tm1Dcp>/Stra8<tm1Dcp>	involves: 129S4/SvJae * C57BL/6	N	16461896
MGI:3625140	M	MP:0001922	reduced male fertility	Prkar1a<tm1Gsm>/Prkar1a<+>	involves: 129X1/SvJ	N	15371594
MGI:3625335	M	MP:0012592	decreased brain choline acetyltransferase activity	Hprt1<b-m3>/Y	B6.129P2-Hprt1<b-m3>	N	7509865
MGI:3625335	M	MP:0003243	abnormal dopaminergic neuron morphology	Hprt1<b-m3>/Y	B6.129P2-Hprt1<b-m3>	N	7509865
MGI:3625335	M	MP:0005643	decreased dopamine level	Hprt1<b-m3>/Y	B6.129P2-Hprt1<b-m3>	N	7509865
MGI:3625335	M	MP:0020078	decreased brain tyrosine 3-monooxygenase activity	Hprt1<b-m3>/Y	B6.129P2-Hprt1<b-m3>	N	7509865
MGI:3625335	M	MP:0003243	abnormal dopaminergic neuron morphology	Hprt1<b-m3>/Y	B6.129P2-Hprt1<b-m3>	N	11297820
MGI:3625338	M	MP:0001441	increased grooming behavior	Hprt1<b-m3>/Y	involves: 129P2/OlaHsd	N	1528024
MGI:3625338	M	MP:0001501	abnormal sleep pattern	Hprt1<b-m3>/Y	involves: 129P2/OlaHsd	N	1528024
MGI:3625448	M	MP:0006362	abnormal male germ cell morphology	Psme4<tm1Slek>/Psme4<tm1Slek>	involves: 129 * C57BL/6	N	16581775
MGI:3625448	M	MP:0001156	abnormal spermatogenesis	Psme4<tm1Slek>/Psme4<tm1Slek>	involves: 129 * C57BL/6	N	16581775
MGI:3625448	M	MP:0006380	abnormal spermatid morphology	Psme4<tm1Slek>/Psme4<tm1Slek>	involves: 129 * C57BL/6	N	16581775
MGI:3625448	M	MP:0001922	reduced male fertility	Psme4<tm1Slek>/Psme4<tm1Slek>	involves: 129 * C57BL/6	N	16581775
MGI:3625448	M	MP:0020550	multinucleated giant male germ cells	Psme4<tm1Slek>/Psme4<tm1Slek>	involves: 129 * C57BL/6	N	16581775
MGI:3625448	M	MP:0002675	asthenozoospermia	Psme4<tm1Slek>/Psme4<tm1Slek>	involves: 129 * C57BL/6	N	16581775
MGI:3625448	M	MP:0005578	teratozoospermia	Psme4<tm1Slek>/Psme4<tm1Slek>	involves: 129 * C57BL/6	N	16581775
MGI:3625448	M	MP:0006379	abnormal spermatocyte morphology	Psme4<tm1Slek>/Psme4<tm1Slek>	involves: 129 * C57BL/6	N	16581775
MGI:3625522	M	MP:0001922	reduced male fertility	Kcnj6<wv>/Kcnj6<wv>	C57BL/6J-Kcnj6<wv>	N	MGI:78029
MGI:3625522	F	MP:0001386	abnormal maternal nurturing	Kcnj6<wv>/Kcnj6<wv>	C57BL/6J-Kcnj6<wv>	N	MGI:78029
MGI:3625522	F	MP:0001923	reduced female fertility	Kcnj6<wv>/Kcnj6<wv>	C57BL/6J-Kcnj6<wv>	N	MGI:78029
MGI:3625524	M	MP:0006380	abnormal spermatid morphology	Kcnj6<wv>/Kcnj6<wv>	B6CBA A<w-J>/A-Kcnj6<wv>	N	10766925
MGI:3625524	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Kcnj6<wv>/Kcnj6<wv>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625524	M	MP:0002216	abnormal seminiferous tubule morphology	Kcnj6<wv>/Kcnj6<wv>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625524	M	MP:0001156	abnormal spermatogenesis	Kcnj6<wv>/Kcnj6<wv>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625524	M	MP:0002674	abnormal sperm motility	Kcnj6<wv>/Kcnj6<wv>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625524	M	MP:0002687	oligozoospermia	Kcnj6<wv>/Kcnj6<wv>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625524	M	MP:0006362	abnormal male germ cell morphology	Kcnj6<wv>/Kcnj6<wv>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625524	M	MP:0002784	abnormal Sertoli cell morphology	Kcnj6<wv>/Kcnj6<wv>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625524	M	MP:0002686	globozoospermia	Kcnj6<wv>/Kcnj6<wv>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625708	M	MP:0002169	no abnormal phenotype detected	Dach2<tm1Mrd>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	16470613
MGI:3625709	M	MP:0002169	no abnormal phenotype detected	Dach2<tm1.1Mrd>/Y	either: (involves: 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6 * FVB) or (involves: 129S7/SvEvBrd * C57BL/6 * ICR)	N	16470613
MGI:3625710	M	MP:0006380	abnormal spermatid morphology	Kcnj6<wv>/Kcnj6<+>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625710	M	MP:0001156	abnormal spermatogenesis	Kcnj6<wv>/Kcnj6<+>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625710	M	MP:0002687	oligozoospermia	Kcnj6<wv>/Kcnj6<+>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625710	M	MP:0006362	abnormal male germ cell morphology	Kcnj6<wv>/Kcnj6<+>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625710	M	MP:0002674	abnormal sperm motility	Kcnj6<wv>/Kcnj6<+>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625710	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Kcnj6<wv>/Kcnj6<+>	B6CBA A<w-J>/A-Kcnj6<wv>	N	7760215
MGI:3625825	M	MP:0005159	azoospermia	Kcnj6<wv>/Kcnj6<wv>	involves: C57BL/6 * CBA/CaGnLe	N	8081012
MGI:3625825	M	MP:0001925	male infertility	Kcnj6<wv>/Kcnj6<wv>	involves: C57BL/6 * CBA/CaGnLe	N	8081012
MGI:3625825	M	MP:0001154	seminiferous tubule degeneration	Kcnj6<wv>/Kcnj6<wv>	involves: C57BL/6 * CBA/CaGnLe	N	9520333
MGI:3625825	M	MP:0002216	abnormal seminiferous tubule morphology	Kcnj6<wv>/Kcnj6<wv>	involves: C57BL/6 * CBA/CaGnLe	N	8081012
MGI:3625825	M	MP:0002631	abnormal epididymis morphology	Kcnj6<wv>/Kcnj6<wv>	involves: C57BL/6 * CBA/CaGnLe	N	8081012
MGI:3625825	M	MP:0001146	abnormal testis morphology	Kcnj6<wv>/Kcnj6<wv>	involves: C57BL/6 * CBA/CaGnLe	N	8081012
MGI:3625825	M	MP:0001154	seminiferous tubule degeneration	Kcnj6<wv>/Kcnj6<wv>	involves: C57BL/6 * CBA/CaGnLe	N	8081012
MGI:3625840	M	MP:0001925	male infertility	Kcnj6<wv>/Kcnj6<+>	involves: C57BL/6J	N	9023358
MGI:3625931	M	MP:0001155	arrest of spermatogenesis	Cadm1<tm1.2Brd>/Cadm1<tm1.2Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	16611999
MGI:3625931	M	MP:0002687	oligozoospermia	Cadm1<tm1.2Brd>/Cadm1<tm1.2Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	16611999
MGI:3625931	M	MP:0005578	teratozoospermia	Cadm1<tm1.2Brd>/Cadm1<tm1.2Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	16611999
MGI:3625931	M	MP:0001925	male infertility	Cadm1<tm1.2Brd>/Cadm1<tm1.2Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	16611999
MGI:3625931	M	MP:0002675	asthenozoospermia	Cadm1<tm1.2Brd>/Cadm1<tm1.2Brd>	involves: 129S7/SvEvBrd * C57BL/6	N	16611999
MGI:3625940	F	MP:0001386	abnormal maternal nurturing	Rab3a<tm1Sud>/Rab3a<tm1Sud>,Rab3c<tm1Sud>/Rab3c<tm1Sud>	involves: 129 * 129P2/OlaHsd	N	15269275
MGI:3625957	M	MP:0005508	abnormal skeleton morphology	Ids<tm1Muen>/Y	Not Specified	N	16505002
MGI:3625957	M	MP:0002152	abnormal brain morphology	Ids<tm1Muen>/Y	Not Specified	N	16505002
MGI:3625957	M	MP:0000414	alopecia	Ids<tm1Muen>/Y	Not Specified	N	16505002
MGI:3625957	M	MP:0001262	decreased body weight	Ids<tm1Muen>/Y	Not Specified	N	12572850
MGI:3625957	M	MP:0008525	decreased cranium height	Ids<tm1Muen>/Y	Not Specified	N	16505002
MGI:3625957	M	MP:0001402	decreased locomotor activity	Ids<tm1Muen>/Y	Not Specified	N	16505002
MGI:3625957	M	MP:0002110	abnormal digit morphology	Ids<tm1Muen>/Y	Not Specified	N	16505002
MGI:3625957	M	MP:0002110	abnormal digit morphology	Ids<tm1Muen>/Y	Not Specified	N	12572850
MGI:3625957	M	MP:0002936	joint swelling	Ids<tm1Muen>/Y	Not Specified	N	12572850
MGI:3625957	M	MP:0002339	abnormal lymph node morphology	Ids<tm1Muen>/Y	Not Specified	N	12572850
MGI:3625957	M	MP:0002882	abnormal neuron morphology	Ids<tm1Muen>/Y	Not Specified	N	12572850
MGI:3625957	M	MP:0001406	abnormal gait	Ids<tm1Muen>/Y	Not Specified	N	16505002
MGI:3625957	M	MP:0001363	increased anxiety-related response	Ids<tm1Muen>/Y	Not Specified	N	16505002
MGI:3625957	M	MP:0001407	short stride length	Ids<tm1Muen>/Y	Not Specified	N	16505002
MGI:3625957	M	MP:0000438	abnormal cranium morphology	Ids<tm1Muen>/Y	Not Specified	N	16505002
MGI:3625957	M	MP:0005059	lysosomal protein accumulation	Ids<tm1Muen>/Y	Not Specified	N	12572850
MGI:3625957	M	MP:0005059	lysosomal protein accumulation	Ids<tm1Muen>/Y	Not Specified	N	16505002
MGI:3625957	M	MP:0001262	decreased body weight	Ids<tm1Muen>/Y	Not Specified	N	16505002
MGI:3625957	M	MP:0002083	premature death	Ids<tm1Muen>/Y	Not Specified	N	16505002
MGI:3626069	F	MP:0001884	mammary gland alveolar hyperplasia	Mtv2<a>/Mtv2<a>	DDD.GR-Mtv2<a>	N	1976120
MGI:3626073	M	MP:0001925	male infertility	Cadm1<tm1Mrkm>/Cadm1<tm1Mrkm>	involves: 129S6/SvEvTac * C57BL/6J	N	16612000
MGI:3626073	M	MP:0002675	asthenozoospermia	Cadm1<tm1Mrkm>/Cadm1<tm1Mrkm>	involves: 129S6/SvEvTac * C57BL/6J	N	16612000
MGI:3626073	M	MP:0001155	arrest of spermatogenesis	Cadm1<tm1Mrkm>/Cadm1<tm1Mrkm>	involves: 129S6/SvEvTac * C57BL/6J	N	16612000
MGI:3626073	M	MP:0009839	multiflagellated sperm	Cadm1<tm1Mrkm>/Cadm1<tm1Mrkm>	involves: 129S6/SvEvTac * C57BL/6J	N	16612000
MGI:3626073	M	MP:0002687	oligozoospermia	Cadm1<tm1Mrkm>/Cadm1<tm1Mrkm>	involves: 129S6/SvEvTac * C57BL/6J	N	16612000
MGI:3626073	M	MP:0004852	decreased testis weight	Cadm1<tm1Mrkm>/Cadm1<tm1Mrkm>	involves: 129S6/SvEvTac * C57BL/6J	N	16612000
MGI:3626073	M	MP:0009239	short sperm flagellum	Cadm1<tm1Mrkm>/Cadm1<tm1Mrkm>	involves: 129S6/SvEvTac * C57BL/6J	N	16612000
MGI:3626073	M	MP:0002686	globozoospermia	Cadm1<tm1Mrkm>/Cadm1<tm1Mrkm>	involves: 129S6/SvEvTac * C57BL/6J	N	16612000
MGI:3626073	M	MP:0005578	teratozoospermia	Cadm1<tm1Mrkm>/Cadm1<tm1Mrkm>	involves: 129S6/SvEvTac * C57BL/6J	N	16612000
MGI:3626074	M	MP:0006378	abnormal spermatogonia morphology	Bdkrb2<tm1Jfh>/Bdkrb2<tm1Jfh>,Ins2<Akita>/Ins2<+>	B6.Cg-Ins2<Akita> Bdkrb2<tm1Jfh>	N	16604193
MGI:3626074	M	MP:0002786	abnormal Leydig cell morphology	Bdkrb2<tm1Jfh>/Bdkrb2<tm1Jfh>,Ins2<Akita>/Ins2<+>	B6.Cg-Ins2<Akita> Bdkrb2<tm1Jfh>	N	16604193
MGI:3626074	M	MP:0010145	abnormal spermatic cord morphology	Bdkrb2<tm1Jfh>/Bdkrb2<tm1Jfh>,Ins2<Akita>/Ins2<+>	B6.Cg-Ins2<Akita> Bdkrb2<tm1Jfh>	N	16604193
MGI:3626074	M	MP:0002216	abnormal seminiferous tubule morphology	Bdkrb2<tm1Jfh>/Bdkrb2<tm1Jfh>,Ins2<Akita>/Ins2<+>	B6.Cg-Ins2<Akita> Bdkrb2<tm1Jfh>	N	16604193
MGI:3626075	M	MP:0011742	decreased urine nitrite level	Bdkrb2<tm1Jfh>/Bdkrb2<tm1Jfh>	B6.129S7-Bdkrb2<tm1Jfh>	N	12560214
MGI:3626075	M	MP:0005367	renal/urinary system phenotype	Bdkrb2<tm1Jfh>/Bdkrb2<tm1Jfh>	B6.129S7-Bdkrb2<tm1Jfh>	Y	12560214
MGI:3626075	M	MP:0002136	abnormal kidney physiology	Bdkrb2<tm1Jfh>/Bdkrb2<tm1Jfh>	B6.129S7-Bdkrb2<tm1Jfh>	N	12560214
MGI:3626075	M	MP:0011320	abnormal glomerular capillary morphology	Bdkrb2<tm1Jfh>/Bdkrb2<tm1Jfh>	B6.129S7-Bdkrb2<tm1Jfh>	N	12560214
MGI:3626075	M	MP:0005386	behavior/neurological phenotype	Bdkrb2<tm1Jfh>/Bdkrb2<tm1Jfh>	B6.129S7-Bdkrb2<tm1Jfh>	Y	12560214
MGI:3626075	M	MP:0002786	abnormal Leydig cell morphology	Bdkrb2<tm1Jfh>/Bdkrb2<tm1Jfh>	B6.129S7-Bdkrb2<tm1Jfh>	N	16604193
MGI:3626075	M	MP:0005385	cardiovascular system phenotype	Bdkrb2<tm1Jfh>/Bdkrb2<tm1Jfh>	B6.129S7-Bdkrb2<tm1Jfh>	Y	12560214
MGI:3626075	M	MP:0005376	homeostasis/metabolism phenotype	Bdkrb2<tm1Jfh>/Bdkrb2<tm1Jfh>	B6.129S7-Bdkrb2<tm1Jfh>	Y	12560214
MGI:3626210	F	MP:0001923	reduced female fertility	Tg(HBB-GH1)420King/0	involves: C57BL/6J * SJL	N	MGI:3625842
MGI:3626284	M	MP:0009856	failure of ejaculation	Ddo<tm1Snyd>/Ddo<tm1Snyd>	involves: 129S4/SvJae	N	16525061
MGI:3628538	M	MP:0001488	increased startle reflex	Gabra3<tm1Dgen>/Y	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3628538	M	MP:0009142	decreased prepulse inhibition	Gabra3<tm1Dgen>/Y	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3628538	M	MP:0001399	hyperactivity	Gabra3<tm1Dgen>/Y	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3628538	M	MP:0031391	increased locomotor activity	Gabra3<tm1Dgen>/Y	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3628543	M	MP:0005559	increased circulating glucose level	Cxcr3<tm1Dgen>/Y	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3628569	M	MP:0001489	decreased startle reflex	Gria3<tm1Dgen>/Y	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3628569	M	MP:0002887	decreased susceptibility to pharmacologically induced seizures	Gria3<tm1Dgen>/Y	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3628569	M	MP:0001973	increased thermal nociceptive threshold	Gria3<tm1Dgen>/Y	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3628573	M	MP:0009142	decreased prepulse inhibition	Gabrq<tm1Dgen>/Y	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3628582	M	MP:0000807	abnormal hippocampus morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0008225	abnormal anterior commissure morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0006254	thin cerebral cortex	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0002152	abnormal brain morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0000790	abnormal stratification in cerebral cortex	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0000813	abnormal hippocampus layer morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0000780	abnormal corpus callosum morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0000781	decreased corpus callosum size	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0008129	absent brain internal capsule	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0008128	abnormal brain internal capsule morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0006300	abnormal entorhinal cortex morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0004077	abnormal striatum morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0000812	abnormal dentate gyrus morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0005277	abnormal brainstem morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0000857	abnormal cerebellar foliation	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0000801	abnormal temporal lobe morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0008221	abnormal hippocampal commissure morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0000852	small cerebellum	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0000832	abnormal thalamus morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0011086	postnatal lethality, incomplete penetrance	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628582	M	MP:0000788	abnormal cerebral cortex morphology	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628583	M	MP:0002906	increased susceptibility to pharmacologically induced seizures	Slc9a6<tm1Dgen>/Y	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3628583	M	MP:0031391	increased locomotor activity	Slc9a6<tm1Dgen>/Y	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3628584	F	MP:0001923	reduced female fertility	Dclk1<tm1Caw>/Dclk1<tm1Caw>,Dcx<tm1Caw>/Dcx<+>	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628593	F	MP:0001923	reduced female fertility	Dclk1<tm1Caw>/Dclk1<+>,Dcx<tm1Caw>/Dcx<+>	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628595	M	MP:0002169	no abnormal phenotype detected	Mtmr1<tm1Dgen>/Y	involves: 129P2/OlaHsd * C57BL/6	N	MGI:3604450
MGI:3628602	M	MP:0002082	postnatal lethality	Dclk1<tm1Caw>/Dclk1<+>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628602	M	MP:0002196	absent corpus callosum	Dclk1<tm1Caw>/Dclk1<+>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628602	M	MP:0008535	enlarged lateral ventricles	Dclk1<tm1Caw>/Dclk1<+>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628602	M	MP:0002152	abnormal brain morphology	Dclk1<tm1Caw>/Dclk1<+>,Dcx<tm1Caw>/Y	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	N	16387638
MGI:3628643	F	MP:0000662	abnormal branching of the mammary ductal tree	Itga2<tm1Ztr>/Itga2<tm1Ztr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	12107118
MGI:3628793	M	MP:0004031	insulitis	H2<i7>/H2<g7>	(NOD x NOD.Cg-H2<i7>)F1	N	8350054
MGI:3628816	F	MP:0013782	abnormal mammary duct terminal end bud morphology	Gsn<tm1Djk>/Gsn<tm1Djk>	involves: 129S4/SvJae * BALB/c	N	10985859
MGI:3628816	F	MP:0006269	abnormal mammary gland growth during pregnancy	Gsn<tm1Djk>/Gsn<tm1Djk>	involves: 129S4/SvJae * BALB/c	N	10985859
MGI:3628816	F	MP:0000662	abnormal branching of the mammary ductal tree	Gsn<tm1Djk>/Gsn<tm1Djk>	involves: 129S4/SvJae * BALB/c	N	10985859
MGI:3628913	M	MP:0002875	decreased erythrocyte cell number	G6pdx<a-m1Neu>/Y	involves: 102/El * C3H/El * T-stock	N	14751857
MGI:3628913	M	MP:0005563	abnormal hemoglobin content	G6pdx<a-m1Neu>/Y	involves: 102/El * C3H/El * T-stock	N	14751857
MGI:3628913	M	MP:0001577	anemia	G6pdx<a-m1Neu>/Y	involves: 102/El * C3H/El * T-stock	N	14751857
MGI:3628913	M	MP:0005562	decreased mean corpuscular hemoglobin	G6pdx<a-m1Neu>/Y	involves: 102/El * C3H/El * T-stock	N	14751857
MGI:3628913	M	MP:0003656	abnormal erythrocyte physiology	G6pdx<a-m1Neu>/Y	involves: 102/El * C3H/El * T-stock	N	14751857
MGI:3628913	M	MP:0000343	abnormal response to cardiac infarction	G6pdx<a-m1Neu>/Y	involves: 102/El * C3H/El * T-stock	N	14757696
MGI:3628913	M	MP:0003186	abnormal redox activity	G6pdx<a-m1Neu>/Y	involves: 102/El * C3H/El * T-stock	N	14751857
MGI:3628913	M	MP:0005602	decreased angiogenesis	G6pdx<a-m1Neu>/Y	involves: 102/El * C3H/El * T-stock	N	12777375
MGI:3628913	M	MP:0002447	abnormal erythrocyte morphology	G6pdx<a-m1Neu>/Y	involves: 102/El * C3H/El * T-stock	N	14751857
MGI:3628913	M	MP:0005397	hematopoietic system phenotype	G6pdx<a-m1Neu>/Y	involves: 102/El * C3H/El * T-stock	Y	3377761
MGI:3628913	M	MP:0005397	hematopoietic system phenotype	G6pdx<a-m1Neu>/Y	involves: 102/El * C3H/El * T-stock	Y	MGI:62169
MGI:3628915	F	MP:0000343	abnormal response to cardiac infarction	G6pdx<a-m1Neu>/G6pdx<a-m1Neu>	involves: 102/El * C3H/El * T-stock	N	14757696
MGI:3628915	F	MP:0005397	hematopoietic system phenotype	G6pdx<a-m1Neu>/G6pdx<a-m1Neu>	involves: 102/El * C3H/El * T-stock	Y	3377761
MGI:3628917	F	MP:0005397	hematopoietic system phenotype	G6pdx<a-m1Neu>/G6pdx<+>	involves: 102/El * C3H/El * T-stock	Y	3377761
MGI:3628921	M	MP:0004938	dilated vasculature	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0001698	decreased embryo size	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0002836	abnormal chorion morphology	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0004937	dilated heart	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0001730	embryonic growth arrest	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0000432	abnormal head morphology	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0004259	small placenta	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0004261	abnormal embryonic neuroepithelium morphology	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0003891	increased allantois apoptosis	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0001914	hemorrhage	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0002085	abnormal embryonic tissue morphology	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0002086	abnormal extraembryonic tissue morphology	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0001688	abnormal somite development	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0001700	abnormal embryo turning	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0012703	decreased embryonic neuroepithelium thickness	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628921	M	MP:0013504	increased embryonic tissue cell apoptosis	G6pdx<tm1Luz>/Y	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0004259	small placenta	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0001716	abnormal placenta labyrinth morphology	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0008029	abnormal paraxial mesoderm morphology	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0001914	hemorrhage	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0002086	abnormal extraembryonic tissue morphology	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0013504	increased embryonic tissue cell apoptosis	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0001614	abnormal blood vessel morphology	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0003891	increased allantois apoptosis	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0003123	paternal imprinting	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0000266	abnormal heart morphology	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0013241	embryo tissue necrosis	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0004255	abnormal spongiotrophoblast layer morphology	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0002836	abnormal chorion morphology	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628922	F	MP:0004261	abnormal embryonic neuroepithelium morphology	G6pdx<tm1Luz>/G6pdx<+>	involves: 129S1/Sv * C57BL/6J	N	12169625
MGI:3628923	M	MP:0002626	increased heart rate	Arrb1<tm1Jse>/Arrb1<tm1Jse>	involves: 129X1/SvJ * Black Swiss	N	9400383
MGI:3628923	M	MP:0001544	abnormal cardiovascular system physiology	Arrb1<tm1Jse>/Arrb1<tm1Jse>	involves: 129X1/SvJ * Black Swiss	N	9400383
MGI:3628923	M	MP:0031635	increased heart left ventricle muscle contractility	Arrb1<tm1Jse>/Arrb1<tm1Jse>	involves: 129X1/SvJ * Black Swiss	N	9400383
MGI:3629056	F	MP:0002080	prenatal lethality	Abcb7<tm1.1Mdf>/Abcb7<+>	involves: 129S4/SvJae * FVB	N	16467350
MGI:3629056	F	MP:0003121	genetic imprinting	Abcb7<tm1.1Mdf>/Abcb7<+>	involves: 129S4/SvJae * FVB	N	16467350
MGI:3629057	M	MP:0002080	prenatal lethality	Abcb7<tm1.1Mdf>/Y	involves: 129S4/SvJae * FVB	N	16467350
MGI:3629058	M	MP:0001914	hemorrhage	Abcb7<tm1Mdf>/Y,Tg(Gata1-cre)1Sho/0	either: (involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N) or (involves: 129S4/SvJae * C57BL/6J * FVB/N)	N	16467350
MGI:3629058	M	MP:0005032	abnormal ectoplacental cone morphology	Abcb7<tm1Mdf>/Y,Tg(Gata1-cre)1Sho/0	either: (involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N) or (involves: 129S4/SvJae * C57BL/6J * FVB/N)	N	16467350
MGI:3629058	M	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance	Abcb7<tm1Mdf>/Y,Tg(Gata1-cre)1Sho/0	either: (involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N) or (involves: 129S4/SvJae * C57BL/6J * FVB/N)	N	16467350
MGI:3629058	M	MP:0003984	embryonic growth retardation	Abcb7<tm1Mdf>/Y,Tg(Gata1-cre)1Sho/0	either: (involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N) or (involves: 129S4/SvJae * C57BL/6J * FVB/N)	N	16467350
MGI:3629059	F	MP:0001914	hemorrhage	Abcb7<tm1Mdf>/Abcb7<+>,Tg(Gata1-cre)1Sho/0	either: (involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N) or (involves: 129S4/SvJae * C57BL/6J * FVB/N)	N	16467350
MGI:3629059	F	MP:0003984	embryonic growth retardation	Abcb7<tm1Mdf>/Abcb7<+>,Tg(Gata1-cre)1Sho/0	either: (involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N) or (involves: 129S4/SvJae * C57BL/6J * FVB/N)	N	16467350
MGI:3629059	F	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance	Abcb7<tm1Mdf>/Abcb7<+>,Tg(Gata1-cre)1Sho/0	either: (involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N) or (involves: 129S4/SvJae * C57BL/6J * FVB/N)	N	16467350
MGI:3629059	F	MP:0005032	abnormal ectoplacental cone morphology	Abcb7<tm1Mdf>/Abcb7<+>,Tg(Gata1-cre)1Sho/0	either: (involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N) or (involves: 129S4/SvJae * C57BL/6J * FVB/N)	N	16467350
MGI:3629061	M	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance	Abcb7<tm1Mdf>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	either: B6.Cg-Edil3<Tg(Sox2-cre)1Amc> Abcb7<tm1Mdf> or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * CBA)	N	16467350
MGI:3629062	F	MP:0010768	mortality/aging	Abcb7<tm1Mdf>/Abcb7<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	either: B6.Cg-Edil3<Tg(Sox2-cre)1Amc> Abcb7<tm1Mdf> or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * CBA)	Y	16467350
MGI:3629063	M	MP:0011091	prenatal lethality, complete penetrance	Abcb7<tm1Mdf>/Y,Tg(Vil1-cre)20Syr/0	either: (involves: 129S4/SvJae * C57BL/6 * DBA/2) or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * DBA/2)	N	16467350
MGI:3629064	F	MP:0011091	prenatal lethality, complete penetrance	Abcb7<tm1Mdf>/Abcb7<+>,Tg(Vil1-cre)20Syr/0	either: (involves: 129S4/SvJae * C57BL/6 * DBA/2) or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * DBA/2)	N	16467350
MGI:3629065	M	MP:0003631	nervous system phenotype	Abcb7<tm1Mdf>/Y,Tg(Nes-cre)1Kln/0	either: B6.Cg-Tg(Nes-cre)1Kln Abcb7<tm1Mdf> or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL)	Y	16467350
MGI:3629065	M	MP:0011085	postnatal lethality, complete penetrance	Abcb7<tm1Mdf>/Y,Tg(Nes-cre)1Kln/0	either: B6.Cg-Tg(Nes-cre)1Kln Abcb7<tm1Mdf> or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL)	N	16467350
MGI:3629065	M	MP:0011088	neonatal lethality, incomplete penetrance	Abcb7<tm1Mdf>/Y,Tg(Nes-cre)1Kln/0	either: B6.Cg-Tg(Nes-cre)1Kln Abcb7<tm1Mdf> or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL)	N	16467350
MGI:3629066	M	MP:0000598	abnormal liver morphology	Abcb7<tm1Mdf>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	either: B6.Cg-Speer6-ps1<Tg(Alb-cre)21Mgn> Abcb7<tm1Mdf> or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * DBA)	N	16467350
MGI:3629066	M	MP:0001570	abnormal circulating enzyme level	Abcb7<tm1Mdf>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	either: B6.Cg-Speer6-ps1<Tg(Alb-cre)21Mgn> Abcb7<tm1Mdf> or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * DBA)	N	16467350
MGI:3629066	M	MP:0005639	hemosiderosis	Abcb7<tm1Mdf>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	either: B6.Cg-Speer6-ps1<Tg(Alb-cre)21Mgn> Abcb7<tm1Mdf> or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * DBA)	N	16467350
MGI:3629066	M	MP:0005584	abnormal enzyme/coenzyme activity	Abcb7<tm1Mdf>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	either: B6.Cg-Speer6-ps1<Tg(Alb-cre)21Mgn> Abcb7<tm1Mdf> or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * DBA)	N	16467350
MGI:3629066	M	MP:0000607	abnormal hepatocyte morphology	Abcb7<tm1Mdf>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	either: B6.Cg-Speer6-ps1<Tg(Alb-cre)21Mgn> Abcb7<tm1Mdf> or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * DBA)	N	16467350
MGI:3629074	F	MP:0001882	abnormal lactation	Nme1<tm1Jyd>/Nme1<tm1Jyd>	129-Nme1<tm1Jyd>	N	12848338
MGI:3629074	F	MP:0000662	abnormal branching of the mammary ductal tree	Nme1<tm1Jyd>/Nme1<tm1Jyd>	129-Nme1<tm1Jyd>	N	12848338
MGI:3629212	F	MP:0001745	increased circulating corticosterone level	Ucn2<tm1Pbl>/Ucn2<tm1Pbl>	involves: 129 * C57BL/6	N	16707802
MGI:3629212	F	MP:0003313	abnormal locomotor activation	Ucn2<tm1Pbl>/Ucn2<tm1Pbl>	involves: 129 * C57BL/6	N	16707802
MGI:3629212	F	MP:0001748	increased circulating adrenocorticotropin level	Ucn2<tm1Pbl>/Ucn2<tm1Pbl>	involves: 129 * C57BL/6	N	16707802
MGI:3629212	F	MP:0001422	abnormal drinking behavior	Ucn2<tm1Pbl>/Ucn2<tm1Pbl>	involves: 129 * C57BL/6	N	16707802
MGI:3629331	F	MP:0009070	small oviduct	Postn<tm1Sjc>/Postn<tm1Sjc>	involves: C57BL/6	N	16314533
MGI:3629331	F	MP:0001127	small ovary	Postn<tm1Sjc>/Postn<tm1Sjc>	involves: C57BL/6	N	16314533
MGI:3629331	F	MP:0003699	abnormal female reproductive system physiology	Postn<tm1Sjc>/Postn<tm1Sjc>	involves: C57BL/6	N	16314533
MGI:3629331	F	MP:0001926	female infertility	Postn<tm1Sjc>/Postn<tm1Sjc>	involves: C57BL/6	N	16314533
MGI:3629331	F	MP:0001923	reduced female fertility	Postn<tm1Sjc>/Postn<tm1Sjc>	involves: C57BL/6	N	16314533
MGI:3629331	F	MP:0009009	absent estrous cycle	Postn<tm1Sjc>/Postn<tm1Sjc>	involves: C57BL/6	N	16314533
MGI:3629331	F	MP:0002637	small uterus	Postn<tm1Sjc>/Postn<tm1Sjc>	involves: C57BL/6	N	16314533
MGI:3629679	M	MP:0001146	abnormal testis morphology	Rbp4<tm1.1Mma>/Rbp4<tm1.1Mma>	involves: 129 * C57BL/6J	N	16586441
MGI:3629679	M	MP:0001156	abnormal spermatogenesis	Rbp4<tm1.1Mma>/Rbp4<tm1.1Mma>	involves: 129 * C57BL/6J	N	16586441
MGI:3629679	M	MP:0006380	abnormal spermatid morphology	Rbp4<tm1.1Mma>/Rbp4<tm1.1Mma>	involves: 129 * C57BL/6J	N	16586441
MGI:3629679	M	MP:0003698	abnormal male reproductive system physiology	Rbp4<tm1.1Mma>/Rbp4<tm1.1Mma>	involves: 129 * C57BL/6J	N	16586441
MGI:3629679	M	MP:0004182	abnormal spermiation	Rbp4<tm1.1Mma>/Rbp4<tm1.1Mma>	involves: 129 * C57BL/6J	N	16586441
MGI:3629699	M	MP:0005669	increased circulating leptin level	Pik3ca<tm1Bvan>/Pik3ca<+>	involves: 129P2/OlaHsd * C57BL/6	N	16625210
MGI:3629699	F	MP:0005293	impaired glucose tolerance	Pik3ca<tm1Bvan>/Pik3ca<+>	involves: 129P2/OlaHsd * C57BL/6	N	16625210
MGI:3629708	M	MP:0002216	abnormal seminiferous tubule morphology	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * C57BL/6	N	33507326
MGI:3629708	M	MP:0001156	abnormal spermatogenesis	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * C57BL/6	N	33507326
MGI:3629708	M	MP:0004852	decreased testis weight	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * C57BL/6	N	33507326
MGI:3629708	M	MP:0004109	abnormal Sertoli cell development	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * C57BL/6	N	33507326
MGI:3629708	M	MP:0004884	abnormal testis physiology	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * C57BL/6	N	33507326
MGI:3629708	M	MP:0003884	decreased macrophage cell number	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * C57BL/6	N	33507326
MGI:3629708	M	MP:0004901	decreased male germ cell number	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * C57BL/6	N	33507326
MGI:3629708	M	MP:0014052	increased male germ cell apoptosis	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * C57BL/6	N	33507326
MGI:3629708	M	MP:0002781	increased circulating testosterone level	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * C57BL/6	N	33507326
MGI:3629708	M	MP:0003205	testicular atrophy	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * C57BL/6	N	33507326
MGI:3629745	M	MP:0005389	reproductive system phenotype	Ar<tm3(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	Y	16400023
MGI:3629745	M	MP:0001260	increased body weight	Ar<tm3(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16601069
MGI:3629745	M	MP:0005378	growth/size/body region phenotype	Ar<tm3(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	Y	16981011
MGI:3629745	M	MP:0003631	nervous system phenotype	Ar<tm3(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	Y	16981011
MGI:3629745	M	MP:0005386	behavior/neurological phenotype	Ar<tm3(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	Y	16981011
MGI:3629745	M	MP:0005458	increased percent body fat/body weight	Ar<tm3(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16601069
MGI:3629745	M	MP:0005369	muscle phenotype	Ar<tm3(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	Y	16981011
MGI:3629746	M	MP:0005458	increased percent body fat/body weight	Ar<tm1(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16601069
MGI:3629746	M	MP:0001260	increased body weight	Ar<tm1(AR)Dmr>/Y	involves: 129S1/Sv * C57BL/6J	N	16601069
MGI:3629749	M	MP:0010357	increased prostate gland tumor incidence	Tg(TRAMP)8247Ng/0	involves: 129S1/Sv * C57BL/6	N	16601069
MGI:3629751	M	MP:0010357	increased prostate gland tumor incidence	Ar<tm1(AR)Dmr>/Y,Tg(TRAMP)8247Ng/0	involves: 129S1/Sv * C57BL/6	N	16601069
MGI:3629752	M	MP:0010357	increased prostate gland tumor incidence	Ar<tm2(AR)Dmr>/Y,Tg(TRAMP)8247Ng/0	involves: 129S1/Sv * C57BL/6	N	16601069
MGI:3629753	M	MP:0002052	decreased tumor incidence	Ar<tm3(AR)Dmr>/Y,Tg(TRAMP)8247Ng/0	involves: 129S1/Sv * C57BL/6	N	16601069
MGI:3629778	F	MP:0011086	postnatal lethality, incomplete penetrance	Gpc3<tm1Arge>/Gpc3<tm1Arge>	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629778	F	MP:0000373	belly spot	Gpc3<tm1Arge>/Gpc3<tm1Arge>	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629778	F	MP:0005388	respiratory system phenotype	Gpc3<tm1Arge>/Gpc3<tm1Arge>	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	Y	11846487
MGI:3629778	F	MP:0004920	increased placenta weight	Gpc3<tm1Arge>/Gpc3<tm1Arge>	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629778	F	MP:0002938	white spotting	Gpc3<tm1Arge>/Gpc3<tm1Arge>	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0011086	postnatal lethality, incomplete penetrance	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0000562	polydactyly	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0005388	respiratory system phenotype	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	Y	11846487
MGI:3629779	M	MP:0000373	belly spot	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0008146	asymmetric sternocostal joints	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0000087	absent mandible	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0000692	small spleen	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0001732	postnatal growth retardation	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0000189	hypoglycemia	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0000522	kidney cortex cyst	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0002705	dilated renal tubule	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0002135	abnormal kidney morphology	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0011307	kidney medulla cyst	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0002938	white spotting	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0001270	distended abdomen	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0000519	hydronephrosis	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0014347	increased spleen B cell follicle size	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0003014	abnormal kidney medulla morphology	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0005584	abnormal enzyme/coenzyme activity	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0001260	increased body weight	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0011308	kidney corticomedullary cyst	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0000477	abnormal intestine morphology	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0003675	kidney cyst	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0004920	increased placenta weight	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0004953	decreased spleen weight	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0011423	kidney cortex atrophy	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629779	M	MP:0011520	increased placental labyrinth size	Gpc3<tm1Arge>/Y	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629781	F	MP:0000373	belly spot	Gpc3<tm1Arge>/Gpc3<+>	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629781	F	MP:0002938	white spotting	Gpc3<tm1Arge>/Gpc3<+>	either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11846487
MGI:3629782	F	MP:0003956	abnormal body size	Gpc3<tm1Arge>/Gpc3<+>,Igf2<tm1Rob>/Igf2<+>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J	N	11846487
MGI:3629782	F	MP:0003122	maternal imprinting	Gpc3<tm1Arge>/Gpc3<+>,Igf2<tm1Rob>/Igf2<+>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J	N	11846487
MGI:3629784	F	MP:0001923	reduced female fertility	Ptgs2<tm1.1Fun>/Ptgs2<tm1.1Fun>	involves: 129S6/SvEvTac * C57BL/6	N	16732282
MGI:3629787	F	MP:0013785	abnormal mammary gland bud morphology	Gli3<Xt-J>/Gli3<Xt-J>	B6.C3-Gli3<Xt-J>/J	N	16720875
MGI:3629787	F	MP:0013720	abnormal mammary line morphology	Gli3<Xt-J>/Gli3<Xt-J>	B6.C3-Gli3<Xt-J>/J	N	16720875
MGI:3629788	F	MP:0013721	abnormal mammary placode morphology	Pax3<tm1Buck>/Pax3<tm1Buck>	involves: 129P2/OlaHsd * C57BL/6	N	16720875
MGI:3629788	F	MP:0013720	abnormal mammary line morphology	Pax3<tm1Buck>/Pax3<tm1Buck>	involves: 129P2/OlaHsd * C57BL/6	N	16720875
MGI:3629789	F	MP:0013721	abnormal mammary placode morphology	Fgf10<tm1Ska>/Fgf10<Tg(Myl3-lacZ)24Buck>	involves: C57BL/6 * CBA	N	16720875
MGI:3629805	M	MP:0004852	decreased testis weight	Pcsk1<N222D>/Pcsk1<N222D>	C57BL/6-Pcsk1<N222D>	N	16644867
MGI:3629805	F	MP:0005669	increased circulating leptin level	Pcsk1<N222D>/Pcsk1<N222D>	C57BL/6-Pcsk1<N222D>	N	16644867
MGI:3629874	M	MP:0003956	abnormal body size	Gpc3<tm1Arge>/Y,Igf2<tm1Rob>/Igf2<+>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J	N	11846487
MGI:3629874	M	MP:0003122	maternal imprinting	Gpc3<tm1Arge>/Y,Igf2<tm1Rob>/Igf2<+>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J	N	11846487
MGI:3629875	M	MP:0011086	postnatal lethality, incomplete penetrance	Gpc3<tm1Arge>/Y,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629875	M	MP:0004920	increased placenta weight	Gpc3<tm1Arge>/Y,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629875	M	MP:0000154	rib fusion	Gpc3<tm1Arge>/Y,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629875	M	MP:0003123	paternal imprinting	Gpc3<tm1Arge>/Y,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629875	M	MP:0004678	split xiphoid process	Gpc3<tm1Arge>/Y,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629875	M	MP:0008277	abnormal sternum ossification	Gpc3<tm1Arge>/Y,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629875	M	MP:0008146	asymmetric sternocostal joints	Gpc3<tm1Arge>/Y,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629875	M	MP:0000480	increased rib number	Gpc3<tm1Arge>/Y,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629875	M	MP:0003052	omphalocele	Gpc3<tm1Arge>/Y,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629875	M	MP:0001260	increased body weight	Gpc3<tm1Arge>/Y,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629875	M	MP:0011090	perinatal lethality, incomplete penetrance	Gpc3<tm1Arge>/Y,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629878	F	MP:0003123	paternal imprinting	Gpc3<tm1Arge>/Gpc3<tm1Arge>,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629878	F	MP:0011090	perinatal lethality, incomplete penetrance	Gpc3<tm1Arge>/Gpc3<tm1Arge>,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629878	F	MP:0011086	postnatal lethality, incomplete penetrance	Gpc3<tm1Arge>/Gpc3<tm1Arge>,H19<tm1Tilg>/H19<+>	involves: 129S/SvEv * 129S1/Sv	N	11846487
MGI:3629887	M	MP:0011089	perinatal lethality, complete penetrance	Gpc3<tm1Arge>/Y,Igf1r<tm1Arge>/Igf1r<tm1Arge>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J	N	11846487
MGI:3629887	M	MP:0009728	abnormal calcaneum morphology	Gpc3<tm1Arge>/Y,Igf1r<tm1Arge>/Igf1r<tm1Arge>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J	N	11846487
MGI:3629887	M	MP:0000556	abnormal hindlimb morphology	Gpc3<tm1Arge>/Y,Igf1r<tm1Arge>/Igf1r<tm1Arge>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J	N	11846487
MGI:3629890	F	MP:0000556	abnormal hindlimb morphology	Gpc3<tm1Arge>/Gpc3<tm1Arge>,Igf1r<tm1Arge>/Igf1r<tm1Arge>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J	N	11846487
MGI:3629890	F	MP:0011089	perinatal lethality, complete penetrance	Gpc3<tm1Arge>/Gpc3<tm1Arge>,Igf1r<tm1Arge>/Igf1r<tm1Arge>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J	N	11846487
MGI:3629890	F	MP:0009728	abnormal calcaneum morphology	Gpc3<tm1Arge>/Gpc3<tm1Arge>,Igf1r<tm1Arge>/Igf1r<tm1Arge>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J	N	11846487
MGI:3629898	F	MP:0011090	perinatal lethality, incomplete penetrance	Gpc3<tm1Arge>/Gpc3<tm1Arge>,Igf1<tm1Arge>/Igf1<tm1Arge>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J * DBA * MF1	N	11846487
MGI:3629898	F	MP:0011085	postnatal lethality, complete penetrance	Gpc3<tm1Arge>/Gpc3<tm1Arge>,Igf1<tm1Arge>/Igf1<tm1Arge>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J * DBA * MF1	N	11846487
MGI:3629900	M	MP:0011090	perinatal lethality, incomplete penetrance	Gpc3<tm1Arge>/Y,Igf1<tm1Arge>/Igf1<tm1Arge>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J * DBA * MF1	N	11846487
MGI:3629900	M	MP:0011085	postnatal lethality, complete penetrance	Gpc3<tm1Arge>/Y,Igf1<tm1Arge>/Igf1<tm1Arge>	involves: 129S/SvEv * 129S1/Sv * C57BL/6J * DBA * MF1	N	11846487
MGI:3629920	F	MP:0004047	abnormal milk composition	Xiap<tm1Vdr>/Xiap<tm1Vdr>	B6.129S1-Xiap<tm1Vdr>	N	15540113
MGI:3629920	F	MP:0013716	hypolactation	Xiap<tm1Vdr>/Xiap<tm1Vdr>	B6.129S1-Xiap<tm1Vdr>	N	15540113
MGI:3629920	F	MP:0000628	abnormal mammary gland development	Xiap<tm1Vdr>/Xiap<tm1Vdr>	B6.129S1-Xiap<tm1Vdr>	N	15540113
MGI:3629933	M	MP:0001146	abnormal testis morphology	Gja4<tm1Paul>/Gja4<tm1Paul>,Gja5<tm1Paul>/Gja5<tm1Paul>	involves: 129S4/SvJae * C57BL/6	N	12435353
MGI:3629933	M	MP:0001156	abnormal spermatogenesis	Gja4<tm1Paul>/Gja4<tm1Paul>,Gja5<tm1Paul>/Gja5<tm1Paul>	involves: 129S4/SvJae * C57BL/6	N	12435353
MGI:3630148	M	MP:0001925	male infertility	Sohlh1<tm1Rajk>/Sohlh1<tm1Rajk>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	16564520
MGI:3630148	M	MP:0004852	decreased testis weight	Sohlh1<tm1Rajk>/Sohlh1<tm1Rajk>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	16564520
MGI:3630148	M	MP:0001156	abnormal spermatogenesis	Sohlh1<tm1Rajk>/Sohlh1<tm1Rajk>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	16564520
MGI:3630148	M	MP:0002216	abnormal seminiferous tubule morphology	Sohlh1<tm1Rajk>/Sohlh1<tm1Rajk>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	16564520
MGI:3630285	F	MP:0002169	no abnormal phenotype detected	Msn<tm1Sts>/Msn<tm1Sts>	involves: 129S4/SvJae * C57BL/6	N	9890997
MGI:3630286	M	MP:0002169	no abnormal phenotype detected	Msn<tm1Sts>/Y	involves: 129S4/SvJae * C57BL/6	N	9890997
MGI:3630286	M	MP:0010856	dilated respiratory conducting tube	Msn<tm1Sts>/Y	involves: 129S4/SvJae * C57BL/6	N	18658275
MGI:3630332	M	MP:0003205	testicular atrophy	Trp53<tm2Xu>/Trp53<tm2Xu>,Xrcc4<tm1Fwa>/Xrcc4<tm1Fwa>	involves: 129P2/OlaHsd * 129S6/SvEvTac	N	16757976
MGI:3630395	F	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-pew3J>/Atp7a<+>	C;B6-Atp7a<Mo-pew3J>/GrsrJ	N	MGI:3037058
MGI:3630396	M	MP:0002083	premature death	Atp7a<Mo-pew3J>/Y	C;B6-Atp7a<Mo-pew3J>/GrsrJ	N	MGI:3037058
MGI:3630396	M	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-pew3J>/Y	C;B6-Atp7a<Mo-pew3J>/GrsrJ	N	MGI:3037058
MGI:3630398	F	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-pew3J>/Atp7a<Mo-pew3J>	C;B6-Atp7a<Mo-pew3J>/GrsrJ	N	MGI:3037058
MGI:3630398	F	MP:0002083	premature death	Atp7a<Mo-pew3J>/Atp7a<Mo-pew3J>	C;B6-Atp7a<Mo-pew3J>/GrsrJ	N	MGI:3037058
MGI:3639079	M	MP:0001940	testis hypoplasia	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	N	14667414
MGI:3639079	M	MP:0005169	abnormal male meiosis	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	N	23318132
MGI:3639079	F	MP:0003582	abnormal ovary development	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	N	14667414
MGI:3639079	F	MP:0002777	absent ovarian follicles	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	N	14667414
MGI:3639079	M	MP:0005159	azoospermia	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	N	14667414
MGI:3639079	M	MP:0008261	arrest of male meiosis	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	N	14667414
MGI:3639081	F	MP:0001386	abnormal maternal nurturing	Xrcc5<tm1Nus>/Xrcc5<tm1Nus>	involves: 129S1/Sv * 129X1/SvJ	N	12531386
MGI:3639106	M	MP:0009763	increased susceptibility to induced morbidity/mortality	Agtr2<tm1Gsb>/Y	FVB.129-Agtr2<tm1Gsb>	N	12624001
MGI:3639106	M	MP:0000230	abnormal systemic arterial blood pressure	Agtr2<tm1Gsb>/Y	FVB.129-Agtr2<tm1Gsb>	N	10373225
MGI:3639106	M	MP:0000250	abnormal vasoconstriction	Agtr2<tm1Gsb>/Y	FVB.129-Agtr2<tm1Gsb>	N	10373225
MGI:3639106	M	MP:0003025	increased vasoconstriction	Agtr2<tm1Gsb>/Y	FVB.129-Agtr2<tm1Gsb>	N	11714657
MGI:3639106	M	MP:0005592	abnormal vascular smooth muscle morphology	Agtr2<tm1Gsb>/Y	FVB.129-Agtr2<tm1Gsb>	N	10373225
MGI:3639106	M	MP:0002753	dilated heart left ventricle	Agtr2<tm1Gsb>/Y	FVB.129-Agtr2<tm1Gsb>	N	12624001
MGI:3639106	M	MP:0001622	abnormal vasculogenesis	Agtr2<tm1Gsb>/Y	FVB.129-Agtr2<tm1Gsb>	N	10373225
MGI:3639106	M	MP:0000343	abnormal response to cardiac infarction	Agtr2<tm1Gsb>/Y	FVB.129-Agtr2<tm1Gsb>	N	12624001
MGI:3639106	M	MP:0002975	vascular smooth muscle hypertrophy	Agtr2<tm1Gsb>/Y	FVB.129-Agtr2<tm1Gsb>	N	11714657
MGI:3639142	M	MP:0002953	thick ventricular wall	Tg(Myh6-Akt1)20Anr/Y	involves: C57BL/6	N	11943770
MGI:3639142	M	MP:0003038	decreased myocardial infarct size	Tg(Myh6-Akt1)20Anr/Y	involves: C57BL/6	N	11943770
MGI:3639142	M	MP:0002625	heart left ventricle hypertrophy	Tg(Myh6-Akt1)20Anr/Y	involves: C57BL/6	N	11943770
MGI:3639142	M	MP:0001625	cardiac hypertrophy	Tg(Myh6-Akt1)20Anr/Y	involves: C57BL/6	N	11943770
MGI:3639148	M	MP:0000230	abnormal systemic arterial blood pressure	Agtr1a<tm1Afu>/Agtr1a<tm1Afu>,Agtr2<tm1Gsb>/Y	mixed	N	12388241
MGI:3639148	M	MP:0011941	increased fluid intake	Agtr1a<tm1Afu>/Agtr1a<tm1Afu>,Agtr2<tm1Gsb>/Y	mixed	N	12388241
MGI:3639679	M	MP:0001148	enlarged testis	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	N	9744866
MGI:3639705	M	MP:0004910	decreased seminal vesicle weight	Gata2<tm1Sac>/Gata2<tm1Sac>,Tg(Cga-cre)3Sac/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL	N	16543408
MGI:3639742	M	MP:0002674	abnormal sperm motility	t<6>/Tagap<tm1Bgh>	involves: BALB/c * BTBR/TF * FVB/N	N	16116428
MGI:3639742	M	MP:0002675	asthenozoospermia	t<6>/Tagap<tm1Bgh>	involves: BALB/c * BTBR/TF * FVB/N	N	16116428
MGI:3639742	M	MP:0005169	abnormal male meiosis	t<6>/Tagap<tm1Bgh>	involves: BALB/c * BTBR/TF * FVB/N	N	16116428
MGI:3639781	M	MP:0001559	hyperglycemia	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	11287097
MGI:3639781	M	MP:0005669	increased circulating leptin level	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	14525913
MGI:3639781	M	MP:0002079	increased circulating insulin level	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	14525913
MGI:3639781	M	MP:0005437	abnormal glycogen level	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	11287097
MGI:3639781	M	MP:0009755	impaired behavioral response to alcohol	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	11826154
MGI:3639781	M	MP:0001261	obese	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	14525913
MGI:3639781	M	MP:0001745	increased circulating corticosterone level	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	14525913
MGI:3639781	M	MP:0002078	abnormal glucose homeostasis	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	11287097
MGI:3639781	M	MP:0005608	cardiac interstitial fibrosis	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	15652259
MGI:3639781	M	MP:0030016	increased adipocyte glucose uptake	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	11287097
MGI:3639781	M	MP:0005333	decreased heart rate	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	15652259
MGI:3639781	M	MP:0005458	increased percent body fat/body weight	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	11287097
MGI:3639781	M	MP:0001007	abnormal sympathetic system morphology	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	15652259
MGI:3639781	M	MP:0009304	increased retroperitoneal fat pad weight	Npy1r<tm1Tped>/Npy1r<tm1Tped>	B6.129P2-Npy1r<tm1Tped>	N	14525913
MGI:3639861	M	MP:0001147	small testis	Dfb/Dfb<+>	BALB/cByJ-Dfb/J	N	MGI:3639593
MGI:3639861	F	MP:0001926	female infertility	Dfb/Dfb<+>	BALB/cByJ-Dfb/J	N	MGI:3639593
MGI:3639938	M	MP:0003205	testicular atrophy	Tert<tm1Rdp>/Tert<tm1Rdp>	B6.Cg-Tert<tm1Rdp>	N	16651430
MGI:3640132	M	MP:0001922	reduced male fertility	Pmp22<Tr>/Pmp22<+>	Not Specified	N	24539699
MGI:3640134	F	MP:0001385	pup cannibalization	Glb1<tm1Jmat>/Glb1<tm1Jmat>	involves: C57BL/6 * CBA * ICR	N	9337086
MGI:3640141	F	MP:0001885	mammary gland duct hyperplasia	Rb1<tm1Fad>/Rb1<tm1Fad>	involves: 129 * C57BL/6	N	19506017
MGI:3640141	F	MP:0000630	mammary gland hyperplasia	Rb1<tm1Fad>/Rb1<tm1Fad>	involves: 129 * C57BL/6	N	19506017
MGI:3640141	F	MP:0003838	abnormal milk ejection	Rb1<tm1Fad>/Rb1<tm1Fad>	involves: 129 * C57BL/6	N	19506017
MGI:3640282	M	MP:0002687	oligozoospermia	Fyn<tm1Sor>/Fyn<tm1Sor>	involves: 129S7/SvEvBrd * C57BL/6J	N	21918125
MGI:3640282	M	MP:0030976	impaired sperm penetration of zona pellucida	Fyn<tm1Sor>/Fyn<tm1Sor>	involves: 129S7/SvEvBrd * C57BL/6J	N	21918125
MGI:3640282	M	MP:0001932	abnormal spermiogenesis	Fyn<tm1Sor>/Fyn<tm1Sor>	involves: 129S7/SvEvBrd * C57BL/6J	N	21918125
MGI:3640282	M	MP:0004542	impaired acrosome reaction	Fyn<tm1Sor>/Fyn<tm1Sor>	involves: 129S7/SvEvBrd * C57BL/6J	N	21918125
MGI:3640282	M	MP:0005578	teratozoospermia	Fyn<tm1Sor>/Fyn<tm1Sor>	involves: 129S7/SvEvBrd * C57BL/6J	N	21918125
MGI:3640282	M	MP:0001156	abnormal spermatogenesis	Fyn<tm1Sor>/Fyn<tm1Sor>	involves: 129S7/SvEvBrd * C57BL/6J	N	21918125
MGI:3640282	M	MP:0009230	abnormal sperm head morphology	Fyn<tm1Sor>/Fyn<tm1Sor>	involves: 129S7/SvEvBrd * C57BL/6J	N	21918125
MGI:3640282	M	MP:0009830	abnormal sperm connecting piece morphology	Fyn<tm1Sor>/Fyn<tm1Sor>	involves: 129S7/SvEvBrd * C57BL/6J	N	21918125
MGI:3640282	M	MP:0004929	decreased epididymis weight	Fyn<tm1Sor>/Fyn<tm1Sor>	involves: 129S7/SvEvBrd * C57BL/6J	N	21918125
MGI:3640282	M	MP:0009647	decreased fertilization frequency	Fyn<tm1Sor>/Fyn<tm1Sor>	involves: 129S7/SvEvBrd * C57BL/6J	N	21918125
MGI:3640282	M	MP:0013286	abnormal sperm capacitation	Fyn<tm1Sor>/Fyn<tm1Sor>	involves: 129S7/SvEvBrd * C57BL/6J	N	21918125
MGI:3640282	M	MP:0005389	reproductive system phenotype	Fyn<tm1Sor>/Fyn<tm1Sor>	involves: 129S7/SvEvBrd * C57BL/6J	Y	21918125
MGI:3640282	M	MP:0002674	abnormal sperm motility	Fyn<tm1Sor>/Fyn<tm1Sor>	involves: 129S7/SvEvBrd * C57BL/6J	N	21918125
MGI:3640296	F	MP:0002169	no abnormal phenotype detected	Xist<tm4.1Nbd>/Xist<+>	involves: 129P2/OlaHsd	N	12900551
MGI:3640310	F	MP:0004047	abnormal milk composition	Csn3<tm1Kuma>/Csn3<tm1Kuma>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	16698927
MGI:3640310	F	MP:0010249	lactation failure	Csn3<tm1Kuma>/Csn3<tm1Kuma>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	16698927
MGI:3640311	F	MP:0004047	abnormal milk composition	Csn3<tm1Kuma>/Csn3<+>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	16698927
MGI:3640321	M	MP:0005669	increased circulating leptin level	Npy5r<tm1Rpa>/Npy5r<tm1Rpa>	involves: 129S7/SvEvBrd	N	14525913
MGI:3640321	M	MP:0009304	increased retroperitoneal fat pad weight	Npy5r<tm1Rpa>/Npy5r<tm1Rpa>	involves: 129S7/SvEvBrd	N	14525913
MGI:3640321	M	MP:0001745	increased circulating corticosterone level	Npy5r<tm1Rpa>/Npy5r<tm1Rpa>	involves: 129S7/SvEvBrd	N	14525913
MGI:3640321	M	MP:0001261	obese	Npy5r<tm1Rpa>/Npy5r<tm1Rpa>	involves: 129S7/SvEvBrd	N	14525913
MGI:3640321	M	MP:0002079	increased circulating insulin level	Npy5r<tm1Rpa>/Npy5r<tm1Rpa>	involves: 129S7/SvEvBrd	N	14525913
MGI:3640332	F	MP:0002907	abnormal parturition	tp/tp	involves: C57BL/10Sn	N	MGI:48789
MGI:3640332	F	MP:0009722	abnormal nipple development	tp/tp	involves: C57BL/10Sn	N	MGI:48789
MGI:3640354	F	MP:0004804	decreased susceptibility to autoimmune diabetes	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	NOD.129S2-Cd40lg<tm1Flv>	N	15467837
MGI:3640354	F	MP:0004974	decreased regulatory T cell number	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	NOD.129S2-Cd40lg<tm1Flv>	N	15467837
MGI:3640356	F	MP:0004031	insulitis	Cd28<tm1Mak>/Cd28<tm1Mak>,Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	NOD.Cg-Cd40lg<tm1Flv> Cd28<tm1Mak>	N	15467837
MGI:3640356	F	MP:0004974	decreased regulatory T cell number	Cd28<tm1Mak>/Cd28<tm1Mak>,Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	NOD.Cg-Cd40lg<tm1Flv> Cd28<tm1Mak>	N	15467837
MGI:3640356	F	MP:0004803	increased susceptibility to autoimmune diabetes	Cd28<tm1Mak>/Cd28<tm1Mak>,Cd40lg<tm1Flv>/Cd40lg<tm1Flv>	NOD.Cg-Cd40lg<tm1Flv> Cd28<tm1Mak>	N	15467837
MGI:3640358	M	MP:0001925	male infertility	Fgfr3<tm5.1Cxd>/Fgfr3<+>	involves: 129S6/SvEvTac	N	11181569
MGI:3640358	F	MP:0001923	reduced female fertility	Fgfr3<tm5.1Cxd>/Fgfr3<+>	involves: 129S6/SvEvTac	N	11181569
MGI:3640483	F	MP:0004855	increased ovary weight	Tg(CAG-Btc)2Ewo/0	FVB/N-Tg(CAG-Btc)2Ewo	N	16179416
MGI:3640485	F	MP:0004855	increased ovary weight	Tg(CAG-Btc)4Ewo/0	FVB/N-Tg(CAG-Btc)4Ewo	N	16179416
MGI:3640503	M	MP:0001156	abnormal spermatogenesis	Stx2<tm1Dcru>/Stx2<tm1Dcru>	involves: 129X1/SvJ * C57BL/6J	N	16710473
MGI:3640503	M	MP:0002216	abnormal seminiferous tubule morphology	Stx2<tm1Dcru>/Stx2<tm1Dcru>	involves: 129X1/SvJ * C57BL/6J	N	16710473
MGI:3640503	M	MP:0001925	male infertility	Stx2<tm1Dcru>/Stx2<tm1Dcru>	involves: 129X1/SvJ * C57BL/6J	N	16710473
MGI:3640503	M	MP:0005159	azoospermia	Stx2<tm1Dcru>/Stx2<tm1Dcru>	involves: 129X1/SvJ * C57BL/6J	N	16710473
MGI:3640503	M	MP:0004852	decreased testis weight	Stx2<tm1Dcru>/Stx2<tm1Dcru>	involves: 129X1/SvJ * C57BL/6J	N	16710473
MGI:3640503	M	MP:0014052	increased male germ cell apoptosis	Stx2<tm1Dcru>/Stx2<tm1Dcru>	involves: 129X1/SvJ * C57BL/6J	N	16710473
MGI:3640659	F	MP:0003316	perineal fistula	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0011780	abnormal female urethra morphology	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0003529	enlarged clitoris	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0013313	female preputial gland hypoplasia	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0001140	abnormal vagina epithelium morphology	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0003541	vaginal inflammation	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0011763	urethritis	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0001923	reduced female fertility	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0001142	abnormal vagina orifice morphology	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0011850	absent clitoral bone	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0001139	abnormal vagina morphology	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0001119	abnormal female reproductive system morphology	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0003315	abnormal perineum morphology	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0003550	short perineum	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640659	F	MP:0011485	abnormal urethra urothelium morphology	Gata5<tm1Eno>/Gata5<tm1Eno>	involves: 129S6/SvEvTac * C57BL/6	N	10866681
MGI:3640957	F	MP:0001923	reduced female fertility	Mos<tm1Gvw>/Mos<tm1Gvw>	involves: 129S1/Sv	N	8692939
MGI:3640957	F	MP:0012737	abnormal primary polar body morphology	Mos<tm1Gvw>/Mos<tm1Gvw>	involves: 129S1/Sv	N	8692939
MGI:3641049	M	MP:0002073	abnormal hair growth	Paf/Y	involves: C3H/HeSn	N	2332613
MGI:3641049	M	MP:0001510	abnormal coat appearance	Paf/Y	involves: C3H/HeSn	N	2332613
MGI:3641049	M	MP:0001930	abnormal meiosis	Paf/Y	involves: C3H/HeSn	N	2332613
MGI:3641049	M	MP:0001929	abnormal gametogenesis	Paf/Y	involves: C3H/HeSn	N	2332613
MGI:3641049	M	MP:0004218	meiotic nondisjunction during M1 phase	Paf/Y	involves: C3H/HeSn	N	2332613
MGI:3641050	F	MP:0002073	abnormal hair growth	Paf/Paf<+>	involves: C3H/HeSn	N	2332613
MGI:3641050	F	MP:0001510	abnormal coat appearance	Paf/Paf<+>	involves: C3H/HeSn	N	2332613
MGI:3641056	F	MP:0001510	abnormal coat appearance	Paf/Paf	involves: C3H/HeSn	N	2332613
MGI:3641056	F	MP:0002073	abnormal hair growth	Paf/Paf	involves: C3H/HeSn	N	2332613
MGI:3641252	F	MP:0008332	decreased lactotroph cell number	Gal<tm1Wyn>/Gal<tm1Wyn>	129P2-Gal<tm1Wyn>	N	9770544
MGI:3641252	F	MP:0001746	abnormal pituitary secretion	Gal<tm1Wyn>/Gal<tm1Wyn>	129P2-Gal<tm1Wyn>	N	9770544
MGI:3641252	F	MP:0000662	abnormal branching of the mammary ductal tree	Gal<tm1Wyn>/Gal<tm1Wyn>	129P2-Gal<tm1Wyn>	N	9770544
MGI:3641252	F	MP:0001882	abnormal lactation	Gal<tm1Wyn>/Gal<tm1Wyn>	129P2-Gal<tm1Wyn>	N	9770544
MGI:3641253	M	MP:0014269	decreased testes secretion	Gal<tm1Wyn>/Gal<tm1Wyn>	involves: 129P2/OlaHsd * C57BL/6	N	12845222
MGI:3641253	M	MP:0004852	decreased testis weight	Gal<tm1Wyn>/Gal<tm1Wyn>	involves: 129P2/OlaHsd * C57BL/6	N	12845222
MGI:3641253	M	MP:0002997	enlarged seminal vesicle	Gal<tm1Wyn>/Gal<tm1Wyn>	involves: 129P2/OlaHsd * C57BL/6	N	12845222
MGI:3641421	F	MP:0001382	abnormal nursing	Xrcc6<tm1Fwa>/Xrcc6<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6J	N	9390689
MGI:3641453	F	MP:0005070	impaired natural killer cell mediated cytotoxicity	Sh2d1a<tm1Lyin>/Sh2d1a<tm1Lyin>	involves: 129S1/Sv * 129X1/SvJ	N	16127454
MGI:3652560	M	MP:0002687	oligozoospermia	Fzd3<tm1Nat>/Fzd3<+>,Fzd6<tm1Nat>/Fzd6<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16495441
MGI:3652560	M	MP:0001922	reduced male fertility	Fzd3<tm1Nat>/Fzd3<+>,Fzd6<tm1Nat>/Fzd6<tm1Nat>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16495441
MGI:3652742	M	MP:0006415	absent testes	Nr5a1<tm3Klp>/Nr5a1<tm3Klp>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	7491115
MGI:3652742	F	MP:0003578	absent ovary	Nr5a1<tm3Klp>/Nr5a1<tm3Klp>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	7491115
MGI:3652791	M	MP:0000249	abnormal blood vessel physiology	Apoe<tm1Unc>/Apoe<tm1Unc>,Timp1<tm1Pds>/Y	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	12538437
MGI:3652862	F	MP:0000628	abnormal mammary gland development	Arhgap5<tm1Jset>/Arhgap5<+>	involves: 129S2/SvPas * C57BL/6	N	12637587
MGI:3652977	F	MP:0005002	abnormal T cell clonal deletion	Cd40lg<tm1Imx>/Cd40lg<tm1Imx>	involves: 129S2/SvPas * C57BL/6J * BALB/c	N	11342622
MGI:3653036	F	MP:0003699	abnormal female reproductive system physiology	Fut2<tm1Sdo>/Fut2<tm1Sdo>	involves: 129X1/SvJ * C57BL/6J	N	14967068
MGI:3653036	F	MP:0004014	abnormal uterine environment	Fut2<tm1Sdo>/Fut2<tm1Sdo>	involves: 129X1/SvJ * C57BL/6J	N	11713270
MGI:3653037	F	MP:0003699	abnormal female reproductive system physiology	Fut2<tm1Sdo>/Fut2<tm1Sdo>	B6.129X1-Fut2<tm1Sdo>	N	15213174
MGI:3653038	M	MP:0003698	abnormal male reproductive system physiology	Fut1<tm1Sdo>/Fut1<tm1Sdo>	involves: 129X1/SvJ * C57BL/6J	N	11713270
MGI:3653205	F	MP:0006269	abnormal mammary gland growth during pregnancy	Rbpj<tm1Hon>/Rbpj<tm1Hon>,Tg(MMTV-cre)1Mam/0	involves: 129P2/OlaHsd * C57BL/6J * FVB * SJL	N	16581056
MGI:3653206	F	MP:0006269	abnormal mammary gland growth during pregnancy	Pofut1<tm2Pst>/Pofut1<tm2Pst>,Tg(MMTV-cre)1Mam/0	involves: 129P2/OlaHsd * FVB	N	16581056
MGI:3653237	M	MP:0001260	increased body weight	Itpr3<tf>/Itpr3<tf>	involves: BTBR	N	23859941
MGI:3653349	F	MP:0001384	abnormal pup retrieval	Fosb<tm1Meg>/Fosb<tm1Meg>	either: (involves: 129S4/SvJae * 129X1/SvJ) or (involves: 129S4/SvJae * 129X1/SvJ * BALB/c)	N	8706134
MGI:3653349	F	MP:0001386	abnormal maternal nurturing	Fosb<tm1Meg>/Fosb<tm1Meg>	either: (involves: 129S4/SvJae * 129X1/SvJ) or (involves: 129S4/SvJae * 129X1/SvJ * BALB/c)	N	8706134
MGI:3653349	F	MP:0001382	abnormal nursing	Fosb<tm1Meg>/Fosb<tm1Meg>	either: (involves: 129S4/SvJae * 129X1/SvJ) or (involves: 129S4/SvJae * 129X1/SvJ * BALB/c)	N	8706134
MGI:3653351	M	MP:0001156	abnormal spermatogenesis	Fos<tm1Pa>/Fos<tm1Pa>	involves: 129X1/SvJ * C57BL/6J	N	1423615
MGI:3653351	F	MP:0001129	impaired ovarian folliculogenesis	Fos<tm1Pa>/Fos<tm1Pa>	involves: 129X1/SvJ * C57BL/6J	N	1423615
MGI:3653351	M	MP:0002216	abnormal seminiferous tubule morphology	Fos<tm1Pa>/Fos<tm1Pa>	involves: 129X1/SvJ * C57BL/6J	N	1423615
MGI:3653351	M	MP:0002673	abnormal sperm number	Fos<tm1Pa>/Fos<tm1Pa>	involves: 129X1/SvJ * C57BL/6J	N	1423615
MGI:3653351	M	MP:0031629	abnormal mounting behavior	Fos<tm1Pa>/Fos<tm1Pa>	involves: 129X1/SvJ * C57BL/6J	N	8025159
MGI:3653482	M	MP:0011228	abnormal vitamin D level	Fgf23<tm1Sliu>/Fgf23<+>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653482	M	MP:0000198	decreased circulating phosphate level	Fgf23<tm1Sliu>/Fgf23<+>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653482	M	MP:0001262	decreased body weight	Fgf23<tm1Sliu>/Fgf23<+>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653482	M	MP:0003116	rickets	Fgf23<tm1Sliu>/Fgf23<+>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653482	M	MP:0004348	long femur	Fgf23<tm1Sliu>/Fgf23<+>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653482	M	MP:0000062	increased bone mineral density	Fgf23<tm1Sliu>/Fgf23<+>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653483	M	MP:0001565	abnormal circulating phosphate level	Fgf23<tm1Sliu>/Fgf23<tm1Sliu>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653483	M	MP:0002083	premature death	Fgf23<tm1Sliu>/Fgf23<tm1Sliu>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653483	M	MP:0011228	abnormal vitamin D level	Fgf23<tm1Sliu>/Fgf23<tm1Sliu>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653483	M	MP:0003116	rickets	Fgf23<tm1Sliu>/Fgf23<tm1Sliu>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653483	M	MP:0002905	decreased circulating parathyroid hormone level	Fgf23<tm1Sliu>/Fgf23<tm1Sliu>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653483	M	MP:0003109	short femur	Fgf23<tm1Sliu>/Fgf23<tm1Sliu>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653483	M	MP:0003055	abnormal long bone epiphyseal plate morphology	Fgf23<tm1Sliu>/Fgf23<tm1Sliu>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653483	M	MP:0001562	abnormal circulating calcium level	Fgf23<tm1Sliu>/Fgf23<tm1Sliu>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653483	M	MP:0000063	decreased bone mineral density	Fgf23<tm1Sliu>/Fgf23<tm1Sliu>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653483	M	MP:0001258	decreased body length	Fgf23<tm1Sliu>/Fgf23<tm1Sliu>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653483	M	MP:0002089	abnormal postnatal growth/weight/body size	Fgf23<tm1Sliu>/Fgf23<tm1Sliu>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653483	M	MP:0001262	decreased body weight	Fgf23<tm1Sliu>/Fgf23<tm1Sliu>,Phex<Hyp>/Y	involves: 129S/SvEv * C57BL/6	N	16449303
MGI:3653485	M	MP:0004686	decreased length of long bones	Phex<Hyp>/Y	Not Specified	N	18172553
MGI:3653485	M	MP:0003109	short femur	Phex<Hyp>/Y	Not Specified	N	18172553
MGI:3653485	M	MP:0000198	decreased circulating phosphate level	Phex<Hyp>/Y	Not Specified	N	18172553
MGI:3653485	M	MP:0001258	decreased body length	Phex<Hyp>/Y	Not Specified	N	16449303
MGI:3653485	M	MP:0000165	abnormal long bone hypertrophic chondrocyte zone	Phex<Hyp>/Y	Not Specified	N	16449303
MGI:3653485	M	MP:0002896	abnormal bone mineralization	Phex<Hyp>/Y	Not Specified	N	16449303
MGI:3653485	M	MP:0011228	abnormal vitamin D level	Phex<Hyp>/Y	Not Specified	N	16449303
MGI:3653485	M	MP:0003116	rickets	Phex<Hyp>/Y	Not Specified	N	16449303
MGI:3653485	M	MP:0009445	osteomalacia	Phex<Hyp>/Y	Not Specified	N	18172553
MGI:3653485	M	MP:0030484	abnormal osteocyte lacuna morphology	Phex<Hyp>/Y	Not Specified	N	18172553
MGI:3653485	M	MP:0001262	decreased body weight	Phex<Hyp>/Y	Not Specified	N	16449303
MGI:3653485	M	MP:0000198	decreased circulating phosphate level	Phex<Hyp>/Y	Not Specified	N	16449303
MGI:3653485	M	MP:0000063	decreased bone mineral density	Phex<Hyp>/Y	Not Specified	N	16449303
MGI:3653485	M	MP:0010110	abnormal renal phosphate reabsorption	Phex<Hyp>/Y	Not Specified	N	18172553
MGI:3653728	F	MP:0001144	vagina atresia	Zeb1<tm2Yhi>/Zeb1<+>,Zeb2<tm1.2Yhi>/Zeb2<+>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	16598713
MGI:3653918	F	MP:0005599	increased cardiac muscle contractility	Hprt1<tm1Dhm>/Hprt1<tm1Dhm>,Pln<tm1Egk>/Pln<tm1Egk>	involves: 129P2/OlaHsd * 129S2/SvPas	N	16461894
MGI:3653918	F	MP:0004084	abnormal cardiac muscle relaxation	Hprt1<tm1Dhm>/Hprt1<tm1Dhm>,Pln<tm1Egk>/Pln<tm1Egk>	involves: 129P2/OlaHsd * 129S2/SvPas	N	16461894
MGI:3653918	F	MP:0004215	abnormal myocardial fiber physiology	Hprt1<tm1Dhm>/Hprt1<tm1Dhm>,Pln<tm1Egk>/Pln<tm1Egk>	involves: 129P2/OlaHsd * 129S2/SvPas	N	16461894
MGI:3653919	M	MP:0004215	abnormal myocardial fiber physiology	Hprt1<tm1Dhm>/Y,Pln<tm1Egk>/Pln<tm1Egk>	involves: 129P2/OlaHsd * 129S2/SvPas	N	16461894
MGI:3653919	M	MP:0004084	abnormal cardiac muscle relaxation	Hprt1<tm1Dhm>/Y,Pln<tm1Egk>/Pln<tm1Egk>	involves: 129P2/OlaHsd * 129S2/SvPas	N	16461894
MGI:3653919	M	MP:0005599	increased cardiac muscle contractility	Hprt1<tm1Dhm>/Y,Pln<tm1Egk>/Pln<tm1Egk>	involves: 129P2/OlaHsd * 129S2/SvPas	N	16461894
MGI:3654338	M	MP:0004852	decreased testis weight	Smtw1<Smt>/Smtw1<Smt>	involves: M. m. molossinus * Smt	N	16651692
MGI:3654339	M	MP:0004852	decreased testis weight	Smtw1<M. m. molossinus>/Smtw1<Smt>	involves: M. m. molossinus * Smt	N	16651692
MGI:3654340	M	MP:0004852	decreased testis weight	Smtw2<Smt>/Y	involves: M. m. molossinus * Smt	N	16651692
MGI:3654341	M	MP:0020550	multinucleated giant male germ cells	Spmd1<Smt>/Spmd1<Smt>	involves: M. m. molossinus * Smt	N	16651692
MGI:3654341	M	MP:0005169	abnormal male meiosis	Spmd1<Smt>/Spmd1<Smt>	involves: M. m. molossinus * Smt	N	16651692
MGI:3654342	M	MP:0002687	oligozoospermia	Spmd2<Smt>/Spmd2<Smt>	involves: M. m. molossinus * Smt	N	16651692
MGI:3654343	M	MP:0002687	oligozoospermia	Spmd2<M. m. molossinus>/Spmd2<Smt>	involves: M. m. molossinus * Smt	N	16651692
MGI:3654344	M	MP:0002687	oligozoospermia	Spmd3<Smt>/Spmd3<Smt>	involves: M. m. molossinus * Smt	N	16651692
MGI:3654345	M	MP:0005169	abnormal male meiosis	Spmd4<Smt>/Spmd4<Smt>	involves: M. m. molossinus * Smt	N	16651692
MGI:3654346	M	MP:0002687	oligozoospermia	Spmd2<Smt>/Spmd2<Smt>,Spmd4<Smt>/Spmd4<Smt>	involves: M. m. molossinus * Smt	N	16651692
MGI:3654552	F	MP:0005621	abnormal cell physiology	Irak1<tm1Wpfl>/Irak1<tm1Wpfl>	involves: 129P2/OlaHsd * C57BL/6J	N	9625767
MGI:3655088	F	MP:0002083	premature death	Dmd<mdx>/Dmd<mdx>,Foxk1<tm1Djg>/Foxk1<tm1Djg>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655088	F	MP:0009419	skeletal muscle fibrosis	Dmd<mdx>/Dmd<mdx>,Foxk1<tm1Djg>/Foxk1<tm1Djg>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655088	F	MP:0011086	postnatal lethality, incomplete penetrance	Dmd<mdx>/Dmd<mdx>,Foxk1<tm1Djg>/Foxk1<tm1Djg>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655088	F	MP:0001402	decreased locomotor activity	Dmd<mdx>/Dmd<mdx>,Foxk1<tm1Djg>/Foxk1<tm1Djg>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655088	F	MP:0003852	skeletal muscle necrosis	Dmd<mdx>/Dmd<mdx>,Foxk1<tm1Djg>/Foxk1<tm1Djg>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655088	F	MP:0000746	weakness	Dmd<mdx>/Dmd<mdx>,Foxk1<tm1Djg>/Foxk1<tm1Djg>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655090	M	MP:0011086	postnatal lethality, incomplete penetrance	Dmd<mdx>/Y,Foxk1<tm1Djg>/Foxk1<tm1Djg>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655090	M	MP:0009419	skeletal muscle fibrosis	Dmd<mdx>/Y,Foxk1<tm1Djg>/Foxk1<tm1Djg>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655090	M	MP:0002083	premature death	Dmd<mdx>/Y,Foxk1<tm1Djg>/Foxk1<tm1Djg>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655090	M	MP:0003852	skeletal muscle necrosis	Dmd<mdx>/Y,Foxk1<tm1Djg>/Foxk1<tm1Djg>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655090	M	MP:0000746	weakness	Dmd<mdx>/Y,Foxk1<tm1Djg>/Foxk1<tm1Djg>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655090	M	MP:0001402	decreased locomotor activity	Dmd<mdx>/Y,Foxk1<tm1Djg>/Foxk1<tm1Djg>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655093	F	MP:0001265	decreased body size	Dmd<mdx>/Dmd<+>,Foxk1<tm1Djg>/Foxk1<+>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655093	F	MP:0003852	skeletal muscle necrosis	Dmd<mdx>/Dmd<+>,Foxk1<tm1Djg>/Foxk1<+>	involves: 129S4/SvJae * C57BL/10ScSn	N	10792059
MGI:3655809	M	MP:0006423	dilated rete testis	Aqp1<tm1Ask>/Aqp1<tm1Ask>	involves: C57BL/6J * CD-1	N	11698654
MGI:3655954	M	MP:0002206	abnormal CNS synaptic transmission	Aff2<tm1Dln>/Y	involves: 129/Sv * C57BL/6	N	11923441
MGI:3655954	M	MP:0003998	decreased thermal nociceptive threshold	Aff2<tm1Dln>/Y	involves: 129/Sv * C57BL/6	N	11923441
MGI:3655954	M	MP:0002083	premature death	Aff2<tm1Dln>/Y	involves: 129/Sv * C57BL/6	N	11923441
MGI:3655954	M	MP:0001463	abnormal spatial learning	Aff2<tm1Dln>/Y	involves: 129/Sv * C57BL/6	N	11923441
MGI:3655954	M	MP:0003008	enhanced long-term potentiation	Aff2<tm1Dln>/Y	involves: 129/Sv * C57BL/6	N	11923441
MGI:3655954	M	MP:0002912	abnormal excitatory postsynaptic potential	Aff2<tm1Dln>/Y	involves: 129/Sv * C57BL/6	N	11923441
MGI:3655954	M	MP:0001454	abnormal cued conditioning behavior	Aff2<tm1Dln>/Y	involves: 129/Sv * C57BL/6	N	11923441
MGI:3655954	M	MP:0001265	decreased body size	Aff2<tm1Dln>/Y	involves: 129/Sv * C57BL/6	N	11923441
MGI:3656008	M	MP:0001145	abnormal male reproductive system morphology	Fgf10<tm1Wss>/Fgf10<tm1Wss>	involves: 129X1/SvJ	N	12941620
MGI:3656008	M	MP:0002770	absent bulbourethral gland	Fgf10<tm1Wss>/Fgf10<tm1Wss>	involves: 129X1/SvJ	N	12941620
MGI:3656008	M	MP:0001158	abnormal prostate gland morphology	Fgf10<tm1Wss>/Fgf10<tm1Wss>	involves: 129X1/SvJ	N	12941620
MGI:3656008	M	MP:0001159	absent prostate gland	Fgf10<tm1Wss>/Fgf10<tm1Wss>	involves: 129X1/SvJ	N	12941620
MGI:3656008	M	MP:0003642	absent seminal vesicle	Fgf10<tm1Wss>/Fgf10<tm1Wss>	involves: 129X1/SvJ	N	12941620
MGI:3656008	M	MP:0003595	epididymal cyst	Fgf10<tm1Wss>/Fgf10<tm1Wss>	involves: 129X1/SvJ	N	12941620
MGI:3656140	F	MP:0011121	decreased primordial ovarian follicle number	Arnt<tm1Gonz>/Arnt<tm1Gonz>,Tg(MMTV-cre)1Mam/0	involves: 129X1/SvJ * FVB	N	11892012
MGI:3656140	F	MP:0001131	abnormal ovarian follicle morphology	Arnt<tm1Gonz>/Arnt<tm1Gonz>,Tg(MMTV-cre)1Mam/0	involves: 129X1/SvJ * FVB	N	11892012
MGI:3656140	F	MP:0001882	abnormal lactation	Arnt<tm1Gonz>/Arnt<tm1Gonz>,Tg(MMTV-cre)1Mam/0	involves: 129X1/SvJ * FVB	N	11892012
MGI:3656140	F	MP:0006269	abnormal mammary gland growth during pregnancy	Arnt<tm1Gonz>/Arnt<tm1Gonz>,Tg(MMTV-cre)1Mam/0	involves: 129X1/SvJ * FVB	N	11892012
MGI:3662691	M	MP:0001914	hemorrhage	F9<tm1Dws>/Y	involves: 129P2/OlaHsd * C57BL/6	N	9354664
MGI:3662691	M	MP:0002551	abnormal blood coagulation	F9<tm1Dws>/Y	involves: 129P2/OlaHsd * C57BL/6	N	9354664
MGI:3662691	M	MP:0002083	premature death	F9<tm1Dws>/Y	involves: 129P2/OlaHsd * C57BL/6	N	9354664
MGI:3662691	M	MP:0000691	enlarged spleen	F9<tm1Dws>/Y	involves: 129P2/OlaHsd * C57BL/6	N	9354664
MGI:3662691	M	MP:0001634	internal hemorrhage	F9<tm1Dws>/Y	involves: 129P2/OlaHsd * C57BL/6	N	9354664
MGI:3662691	M	MP:0005385	cardiovascular system phenotype	F9<tm1Dws>/Y	involves: 129P2/OlaHsd * C57BL/6	Y	12426405
MGI:3662734	F	MP:0001523	impaired righting response	Fgf3<tm1Mrc>/Fgf3<tm1Mrc>	involves: 129S7/SvEvBrd * C57BL/6	N	8223243
MGI:3662734	F	MP:0001394	circling	Fgf3<tm1Mrc>/Fgf3<tm1Mrc>	involves: 129S7/SvEvBrd * C57BL/6	N	8223243
MGI:3662734	F	MP:0006358	absent pinna reflex	Fgf3<tm1Mrc>/Fgf3<tm1Mrc>	involves: 129S7/SvEvBrd * C57BL/6	N	8223243
MGI:3662734	F	MP:0001399	hyperactivity	Fgf3<tm1Mrc>/Fgf3<tm1Mrc>	involves: 129S7/SvEvBrd * C57BL/6	N	8223243
MGI:3662734	F	MP:0001489	decreased startle reflex	Fgf3<tm1Mrc>/Fgf3<tm1Mrc>	involves: 129S7/SvEvBrd * C57BL/6	N	8223243
MGI:3662841	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tbx21<tm1Glm>/Tbx21<tm1Glm>,Tg(TRAMP)8247Ng/0	involves: 129S6/SvEvTac * C57BL/6	N	14744755
MGI:3662841	M	MP:0010357	increased prostate gland tumor incidence	Tbx21<tm1Glm>/Tbx21<tm1Glm>,Tg(TRAMP)8247Ng/0	involves: 129S6/SvEvTac * C57BL/6	N	14744755
MGI:3662841	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tbx21<tm1Glm>/Tbx21<tm1Glm>,Tg(TRAMP)8247Ng/0	involves: 129S6/SvEvTac * C57BL/6	N	14744755
MGI:3662841	M	MP:0001272	increased metastatic potential	Tbx21<tm1Glm>/Tbx21<tm1Glm>,Tg(TRAMP)8247Ng/0	involves: 129S6/SvEvTac * C57BL/6	N	14744755
MGI:3662853	M	MP:0005606	increased bleeding time	F9<tm1Emg>/Y	involves: 129S/SvEv * C57BL/6J	N	9639513
MGI:3662853	M	MP:0001914	hemorrhage	F9<tm1Emg>/Y	involves: 129S/SvEv * C57BL/6J	N	9639513
MGI:3662853	M	MP:0002551	abnormal blood coagulation	F9<tm1Emg>/Y	involves: 129S/SvEv * C57BL/6J	N	9639513
MGI:3662853	M	MP:0005370	liver/biliary system phenotype	F9<tm1Emg>/Y	involves: 129S/SvEv * C57BL/6J	Y	9639513
MGI:3662853	M	MP:0011086	postnatal lethality, incomplete penetrance	F9<tm1Emg>/Y	involves: 129S/SvEv * C57BL/6J	N	9639513
MGI:3662853	M	MP:0012305	umbilical cord hemorrhage	F9<tm1Emg>/Y	involves: 129S/SvEv * C57BL/6J	N	9639513
MGI:3662854	F	MP:0031434	increased miscarriage rate	Fgg<tm1Fjc>/Fgg<tm1Fjc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11891199
MGI:3662854	F	MP:0004898	uterine hemorrhage	Fgg<tm1Fjc>/Fgg<tm1Fjc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11891199
MGI:3662883	F	MP:0005391	vision/eye phenotype	Glra2<tm1Clc>/Glra2<tm1Clc>	involves: 129X1/SvJ	Y	16847326
MGI:3662883	F	MP:0005389	reproductive system phenotype	Glra2<tm1Clc>/Glra2<tm1Clc>	involves: 129X1/SvJ	Y	16847326
MGI:3662883	F	MP:0005386	behavior/neurological phenotype	Glra2<tm1Clc>/Glra2<tm1Clc>	involves: 129X1/SvJ	Y	16847326
MGI:3662883	F	MP:0003463	abnormal single cell response	Glra2<tm1Clc>/Glra2<tm1Clc>	involves: 129X1/SvJ	N	16847326
MGI:3663045	F	MP:0009375	thin zona pellucida	Zp3<tm1Dean>/Zp3<tm1Dean>,Tg(ZP3)7812Dean/?	involves: 129S4/SvJae * C57BL/6J * FVB/N	N	12852850
MGI:3663104	F	MP:0004771	increased anti-single stranded DNA antibody level	C4b<tm1Crr>/C4b<tm1Crr>	involves: 129S4/SvJae * C57BL/6J	N	11067882
MGI:3663104	F	MP:0004762	increased anti-double stranded DNA antibody level	C4b<tm1Crr>/C4b<tm1Crr>	involves: 129S4/SvJae * C57BL/6J	N	11067882
MGI:3663104	F	MP:0004794	increased anti-nuclear antigen antibody level	C4b<tm1Crr>/C4b<tm1Crr>	involves: 129S4/SvJae * C57BL/6J	N	11067882
MGI:3663104	F	MP:0005325	abnormal renal glomerulus morphology	C4b<tm1Crr>/C4b<tm1Crr>	involves: 129S4/SvJae * C57BL/6J	N	11067882
MGI:3663104	F	MP:0002743	glomerulonephritis	C4b<tm1Crr>/C4b<tm1Crr>	involves: 129S4/SvJae * C57BL/6J	N	11067882
MGI:3663104	F	MP:0004952	increased spleen weight	C4b<tm1Crr>/C4b<tm1Crr>	involves: 129S4/SvJae * C57BL/6J	N	11067882
MGI:3663104	F	MP:0020518	renal glomerular protein deposits	C4b<tm1Crr>/C4b<tm1Crr>	involves: 129S4/SvJae * C57BL/6J	N	11067882
MGI:3663129	M	MP:0001393	ataxia	Fgf14<tm1Dor>/Fgf14<tm1Dor>	B6.129S6-Fgf14<tm1Dor>	N	17236779
MGI:3663129	M	MP:0031391	increased locomotor activity	Fgf14<tm1Dor>/Fgf14<tm1Dor>	B6.129S6-Fgf14<tm1Dor>	N	17236779
MGI:3663129	M	MP:0001405	impaired coordination	Fgf14<tm1Dor>/Fgf14<tm1Dor>	B6.129S6-Fgf14<tm1Dor>	N	17236779
MGI:3663129	M	MP:0012307	impaired spatial learning	Fgf14<tm1Dor>/Fgf14<tm1Dor>	B6.129S6-Fgf14<tm1Dor>	N	17236779
MGI:3663129	M	MP:0010053	decreased grip strength	Fgf14<tm1Dor>/Fgf14<tm1Dor>	B6.129S6-Fgf14<tm1Dor>	N	17236779
MGI:3663129	M	MP:0001473	reduced long-term potentiation	Fgf14<tm1Dor>/Fgf14<tm1Dor>	B6.129S6-Fgf14<tm1Dor>	N	17236779
MGI:3663630	F	MP:0009352	impaired spacing of implantation sites	Axin1<Fu-kb>/Axin1<Fu-kb>	Not Specified	N	MGI:62029
MGI:3663630	F	MP:0009353	twin decidual capsule	Axin1<Fu-kb>/Axin1<Fu-kb>	Not Specified	N	MGI:62029
MGI:3663778	F	MP:0001926	female infertility	Fga<tm1Jld>/Fga<tm1Jld>	involves: 129P2/OlaHsd * CF-1	N	7649481
MGI:3663778	F	MP:0004014	abnormal uterine environment	Fga<tm1Jld>/Fga<tm1Jld>	involves: 129P2/OlaHsd * CF-1	N	7649481
MGI:3663778	F	MP:0004898	uterine hemorrhage	Fga<tm1Jld>/Fga<tm1Jld>	involves: 129P2/OlaHsd * CF-1	N	7649481
MGI:3663779	F	MP:0004898	uterine hemorrhage	Fga<tm1Jld>/Fga<tm1Jld>	B6.129P2-Fga<tm1Jld>	N	7649481
MGI:3663779	F	MP:0004014	abnormal uterine environment	Fga<tm1Jld>/Fga<tm1Jld>	B6.129P2-Fga<tm1Jld>	N	7649481
MGI:3663779	F	MP:0001926	female infertility	Fga<tm1Jld>/Fga<tm1Jld>	B6.129P2-Fga<tm1Jld>	N	7649481
MGI:3664023	M	MP:0011089	perinatal lethality, complete penetrance	Tg(Myh6-Lef1)2Tfo/Y	involves: C57BL/6J * FVB/N	N	16738313
MGI:3664097	M	MP:0011940	decreased food intake	Ptpn1<tm2Bbk>/Ptpn1<tm2Bbk>,Tg(Nes-cre)1Kln/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	16845389
MGI:3664454	F	MP:0001923	reduced female fertility	Tg(ZP2)2Dean/0,Zp2<tm1Dean>/Zp2<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * CF-1 * FVB/N	N	12852850
MGI:3664455	F	MP:0001923	reduced female fertility	Tg(ZP2)2Dean/0,Tg(ZP3)7812Dean/?,Zp2<tm1Dean>/Zp2<tm1Dean>,Zp3<tm1Dean>/Zp3<tm1Dean>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CF-1 * FVB/N	N	12852850
MGI:3664551	M	MP:0001940	testis hypoplasia	Ncoa1<tm1.1Hkaw>/Ncoa1<tm1.1Hkaw>	B6.Cg-Ncoa1<tm1.1Hkaw>	N	15312245
MGI:3664726	F	MP:0001882	abnormal lactation	Adipoq<tm1Far>/Adipoq<tm1Far>,Dgat1<tm1Far>/Dgat1<tm1Far>	involves: 129S4/SvJae * C57BL/6J	N	16595853
MGI:3664738	M	MP:0002085	abnormal embryonic tissue morphology	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0000706	small thymus	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0000245	abnormal erythropoiesis	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0000334	decreased granulocyte number	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0008208	decreased pro-B cell number	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0001823	thymus hypoplasia	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0001577	anemia	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0003884	decreased macrophage cell number	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0000238	absent pre-B cells	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0005092	decreased double-positive T cell number	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0000746	weakness	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0000703	abnormal thymus morphology	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0002145	abnormal T cell differentiation	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0002144	abnormal B cell differentiation	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0000333	decreased bone marrow cell number	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0002080	prenatal lethality	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0002058	neonatal lethality	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0001601	abnormal myelopoiesis	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0002083	premature death	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0000715	decreased thymocyte number	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0008215	decreased immature B cell number	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0000208	decreased hematocrit	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0004809	increased hematopoietic stem cell number	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664738	M	MP:0002123	abnormal definitive hematopoiesis	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Y	involves: 129S4/SvJae	N	16980619
MGI:3664739	F	MP:0000333	decreased bone marrow cell number	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Xist<tm1Awu>	involves: 129S4/SvJae	N	16980619
MGI:3664739	F	MP:0002083	premature death	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Xist<tm1Awu>	involves: 129S4/SvJae	N	16980619
MGI:3664739	F	MP:0000706	small thymus	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Xist<tm1Awu>	involves: 129S4/SvJae	N	16980619
MGI:3664739	F	MP:0000746	weakness	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Xist<tm1Awu>	involves: 129S4/SvJae	N	16980619
MGI:3664739	F	MP:0000208	decreased hematocrit	Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>,Xist<tm1Awu>/Xist<tm1Awu>	involves: 129S4/SvJae	N	16980619
MGI:3664785	M	MP:0001925	male infertility	Grm1<crv4>/Grm1<crv4>	BALB/cPas-Grm1<crv4>	N	16964410
MGI:3664785	F	MP:0001923	reduced female fertility	Grm1<crv4>/Grm1<crv4>	BALB/cPas-Grm1<crv4>	N	16964410
MGI:3664802	F	MP:0001263	weight loss	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae * C57BL/6	N	15947421
MGI:3664802	F	MP:0005388	respiratory system phenotype	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae * C57BL/6	Y	15947421
MGI:3664802	F	MP:0000219	increased neutrophil cell number	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae * C57BL/6	N	15947421
MGI:3664802	F	MP:0003070	increased vascular permeability	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae * C57BL/6	N	15947421
MGI:3664802	F	MP:0001182	lung hemorrhage	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae * C57BL/6	N	15947421
MGI:3664802	F	MP:0009763	increased susceptibility to induced morbidity/mortality	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae * C57BL/6	N	15947421
MGI:3664802	F	MP:0001861	lung inflammation	Timp1<tm1Pds>/Timp1<tm1Pds>	involves: 129S4/SvJae * C57BL/6	N	15947421
MGI:3664861	M	MP:0001153	small seminiferous tubules	B4galt1<tm1Shur>/B4galt1<tm1Shur>	involves: 129S7/SvEvBrd * C57BL/6J	N	9013935
MGI:3664861	M	MP:0004542	impaired acrosome reaction	B4galt1<tm1Shur>/B4galt1<tm1Shur>	involves: 129S7/SvEvBrd * C57BL/6J	N	9374408
MGI:3664861	M	MP:0002674	abnormal sperm motility	B4galt1<tm1Shur>/B4galt1<tm1Shur>	involves: 129S7/SvEvBrd * C57BL/6J	N	9374408
MGI:3664861	F	MP:0002293	long gestation period	B4galt1<tm1Shur>/B4galt1<tm1Shur>	involves: 129S7/SvEvBrd * C57BL/6J	N	9374408
MGI:3664861	F	MP:0010249	lactation failure	B4galt1<tm1Shur>/B4galt1<tm1Shur>	involves: 129S7/SvEvBrd * C57BL/6J	N	9013935
MGI:3664861	M	MP:0001156	abnormal spermatogenesis	B4galt1<tm1Shur>/B4galt1<tm1Shur>	involves: 129S7/SvEvBrd * C57BL/6J	N	9013935
MGI:3664861	M	MP:0004543	abnormal sperm physiology	B4galt1<tm1Shur>/B4galt1<tm1Shur>	involves: 129S7/SvEvBrd * C57BL/6J	N	9374408
MGI:3664861	F	MP:0004514	dystocia	B4galt1<tm1Shur>/B4galt1<tm1Shur>	involves: 129S7/SvEvBrd * C57BL/6J	N	9013935
MGI:3665169	F	MP:0002169	no abnormal phenotype detected	S100g<del1>/S100g<del1>	129P2/OlaHsd-S100g<del1>	N	16895982
MGI:3665265	F	MP:0001885	mammary gland duct hyperplasia	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	N	16943438
MGI:3665265	F	MP:0009092	endometrium hyperplasia	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	N	16943438
MGI:3665265	F	MP:0000630	mammary gland hyperplasia	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	N	16943438
MGI:3665265	F	MP:0009503	abnormal mammary gland duct morphology	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	N	16943438
MGI:3665265	F	MP:0001138	abnormal uterine cervix squamous epithelium morphology	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	N	16943438
MGI:3665265	F	MP:0000627	abnormal mammary gland morphology	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	N	16943438
MGI:3665265	F	MP:0009504	abnormal mammary gland epithelium morphology	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	N	16943438
MGI:3665288	M	MP:0001925	male infertility	Tg(Gfap-TK)7.1Mvs/0	involves: C57BL/10 * CBA * CFLP	N	9568712
MGI:3665430	F	MP:0001923	reduced female fertility	Gt(ROSA)26Sor<tm2(CAG-Dsred2/EGFP)Luo>/Gt(ROSA)26Sor<tm2(CAG-Dsred2/EGFP)Luo>	involves: 129S1/Sv * 129X1/SvJ	N	MGI:3665425
MGI:3665452	F	MP:0000628	abnormal mammary gland development	Ntn1<Gt(ST629)Byg>/Ntn1<Gt(ST629)Byg>	involves: 129P2/OlaHsd	N	12636918
MGI:3665463	F	MP:0000628	abnormal mammary gland development	Neo1<Gt(KST265)Byg>/Neo1<Gt(KST265)Byg>	involves: 129P2/OlaHsd	N	12636918
MGI:3665480	M	MP:0003820	increased left ventricle systolic pressure	Wrn<tm1Led>/Wrn<tm1Led>	B6.129S6(BKSW)-Wrn<tm1Led>	N	16330174
MGI:3665480	F	MP:0005178	increased circulating cholesterol level	Wrn<tm1Led>/Wrn<tm1Led>	B6.129S6(BKSW)-Wrn<tm1Led>	N	16330174
MGI:3665480	M	MP:0014427	increased circulating hyaluronic acid level	Wrn<tm1Led>/Wrn<tm1Led>	B6.129S6(BKSW)-Wrn<tm1Led>	N	16330174
MGI:3665480	M	MP:0006263	decreased systemic arterial diastolic blood pressure	Wrn<tm1Led>/Wrn<tm1Led>	B6.129S6(BKSW)-Wrn<tm1Led>	N	16330174
MGI:3665480	M	MP:0006117	aortic valve stenosis	Wrn<tm1Led>/Wrn<tm1Led>	B6.129S6(BKSW)-Wrn<tm1Led>	N	16330174
MGI:3665578	M	MP:0001925	male infertility	Unc5c<rcm>/Unc5c<rcm>	C57BL/6J-Unc5c<rcm>	N	MGI:62439
MGI:3665578	M	MP:0001925	male infertility	Unc5c<rcm>/Unc5c<rcm>	C57BL/6J-Unc5c<rcm>	N	1401878
MGI:3686854	F	MP:0003231	abnormal placenta vasculature	Esx1<tm1Bhr>/Esx1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:3686854	F	MP:0004201	fetal growth retardation	Esx1<tm1Bhr>/Esx1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:3686854	F	MP:0011531	abnormal syncytiotrophoblast morphology	Esx1<tm1Bhr>/Esx1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:3686854	F	MP:0001265	decreased body size	Esx1<tm1Bhr>/Esx1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:3686854	F	MP:0004920	increased placenta weight	Esx1<tm1Bhr>/Esx1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:3686854	F	MP:0005031	abnormal trophoblast layer morphology	Esx1<tm1Bhr>/Esx1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:3686854	F	MP:0012108	increased trophoblast glycogen cell number	Esx1<tm1Bhr>/Esx1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:3686854	F	MP:0005378	growth/size/body region phenotype	Esx1<tm1Bhr>/Esx1<+>	involves: 129S7/SvEvBrd * C57BL/6	Y	9806555
MGI:3686854	F	MP:0005380	embryo phenotype	Esx1<tm1Bhr>/Esx1<+>	involves: 129S7/SvEvBrd * C57BL/6	Y	9806555
MGI:3686854	F	MP:0004255	abnormal spongiotrophoblast layer morphology	Esx1<tm1Bhr>/Esx1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:3686854	F	MP:0001712	abnormal placenta development	Esx1<tm1Bhr>/Esx1<+>	involves: 129S7/SvEvBrd * C57BL/6	N	9806555
MGI:3687265	M	MP:0003984	embryonic growth retardation	Aifm1<tm2Pngr>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129P2/OlaHsd * FVB/N	N	16287843
MGI:3687265	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Aifm1<tm2Pngr>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129P2/OlaHsd * FVB/N	N	16287843
MGI:3687266	F	MP:0001265	decreased body size	Aifm1<tm2Pngr>/Aifm1<+>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129P2/OlaHsd * FVB/N	N	16287843
MGI:3687266	F	MP:0011101	prenatal lethality, incomplete penetrance	Aifm1<tm2Pngr>/Aifm1<+>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129P2/OlaHsd * FVB/N	N	16287843
MGI:3687267	M	MP:0008775	abnormal heart ventricle pressure	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0000749	muscle degeneration	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0003953	abnormal hormone level	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0005202	lethargy	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0003084	abnormal skeletal muscle fiber morphology	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0000278	abnormal myocardial fiber morphology	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0003674	oxidative stress	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0010957	abnormal aerobic respiration	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0010955	abnormal respiratory electron transport chain	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0001263	weight loss	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0011628	increased mitochondrial number	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0002795	dilated cardiomyopathy	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0004564	increased myocardial fiber size	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0011594	decreased catalase activity	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0001625	cardiac hypertrophy	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0006035	abnormal mitochondrial morphology	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0006036	abnormal mitochondrial physiology	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0009401	increased skeletal muscle fiber diameter	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0002078	abnormal glucose homeostasis	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0013405	increased circulating lactate level	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0005140	decreased cardiac muscle contractility	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0004819	decreased skeletal muscle mass	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0002269	muscular atrophy	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687267	M	MP:0000274	enlarged heart	Aifm1<tm2Pngr>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	16287843
MGI:3687280	M	MP:0006039	decreased mitochondrial fission	Aifm1<tm2Pngr>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd	N	16917506
MGI:3687280	M	MP:0006254	thin cerebral cortex	Aifm1<tm2Pngr>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd	N	16917506
MGI:3687280	M	MP:0006035	abnormal mitochondrial morphology	Aifm1<tm2Pngr>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd	N	16917506
MGI:3687280	M	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance	Aifm1<tm2Pngr>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd	N	16917506
MGI:3687280	M	MP:0003204	decreased neuron apoptosis	Aifm1<tm2Pngr>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd	N	16917506
MGI:3687280	M	MP:0005319	abnormal enzyme/coenzyme level	Aifm1<tm2Pngr>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd	N	16917506
MGI:3687280	M	MP:0006036	abnormal mitochondrial physiology	Aifm1<tm2Pngr>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd	N	16917506
MGI:3687280	M	MP:0003203	increased neuron apoptosis	Aifm1<tm2Pngr>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd	N	16917506
MGI:3687281	M	MP:0000789	thickened cerebral cortex	Apaf1<Gt(IRESBetageo)XIX18Pgr>/Apaf1<Gt(IRESBetageo)XIX18Pgr>,Aifm1<tm2Pngr>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	N	16917506
MGI:3687281	M	MP:0006036	abnormal mitochondrial physiology	Apaf1<Gt(IRESBetageo)XIX18Pgr>/Apaf1<Gt(IRESBetageo)XIX18Pgr>,Aifm1<tm2Pngr>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	N	16917506
MGI:3687281	M	MP:0003204	decreased neuron apoptosis	Apaf1<Gt(IRESBetageo)XIX18Pgr>/Apaf1<Gt(IRESBetageo)XIX18Pgr>,Aifm1<tm2Pngr>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	N	16917506
MGI:3687281	M	MP:0003203	increased neuron apoptosis	Apaf1<Gt(IRESBetageo)XIX18Pgr>/Apaf1<Gt(IRESBetageo)XIX18Pgr>,Aifm1<tm2Pngr>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	N	16917506
MGI:3687325	F	MP:0001545	abnormal hematopoietic system physiology	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0000208	decreased hematocrit	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0000691	enlarged spleen	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0005017	decreased B cell number	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0000218	increased leukocyte cell number	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0010373	myeloid hyperplasia	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0000219	increased neutrophil cell number	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0000693	spleen hyperplasia	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0000598	abnormal liver morphology	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0001175	abnormal lung morphology	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0008826	abnormal splenic cell ratio	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0002357	abnormal spleen white pulp morphology	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0001577	anemia	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0002875	decreased erythrocyte cell number	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0002396	abnormal hematopoietic system morphology/development	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0000702	enlarged lymph nodes	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687325	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	N	17018605
MGI:3687375	M	MP:0004928	increased epididymis weight	Cxcr2<tm1Mwm>/Cxcr2<tm1Mwm>	involves: 129S2/SvPas * BALB/c	N	16094689
MGI:3687375	M	MP:0004909	increased seminal vesicle weight	Cxcr2<tm1Mwm>/Cxcr2<tm1Mwm>	involves: 129S2/SvPas * BALB/c	N	16094689
MGI:3687460	M	MP:0001145	abnormal male reproductive system morphology	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	16717126
MGI:3687460	M	MP:0008261	arrest of male meiosis	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	16717126
MGI:3687460	F	MP:0001923	reduced female fertility	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	16717126
MGI:3687460	M	MP:0001925	male infertility	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	16717126
MGI:3687460	M	MP:0001146	abnormal testis morphology	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	16717126
MGI:3687460	F	MP:0005168	abnormal female meiosis	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	16717126
MGI:3687460	M	MP:0014052	increased male germ cell apoptosis	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	16717126
MGI:3687460	M	MP:0001153	small seminiferous tubules	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	16717126
MGI:3687460	M	MP:0005159	azoospermia	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	16717126
MGI:3687460	M	MP:0004852	decreased testis weight	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	16717126
MGI:3687508	F	MP:0008211	decreased mature B cell number	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Cd79a<tm1(cre)Reth>/Cd79a<+>	involves: BALB/c * C57BL/6	N	16782029
MGI:3687508	F	MP:0005017	decreased B cell number	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Cd79a<tm1(cre)Reth>/Cd79a<+>	involves: BALB/c * C57BL/6	N	16782029
MGI:3687508	F	MP:0002144	abnormal B cell differentiation	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Cd79a<tm1(cre)Reth>/Cd79a<+>	involves: BALB/c * C57BL/6	N	16782029
MGI:3687743	F	MP:0002467	impaired neutrophil phagocytosis	Btk<xid>/Btk<xid>	CBA/CaHN-Btk<xid>/J	N	15117762
MGI:3687743	F	MP:0008537	increased susceptibility to induced colitis	Btk<xid>/Btk<xid>	CBA/CaHN-Btk<xid>/J	N	15117762
MGI:3687743	F	MP:0002463	abnormal neutrophil physiology	Btk<xid>/Btk<xid>	CBA/CaHN-Btk<xid>/J	N	15117762
MGI:3687743	F	MP:0002451	abnormal macrophage physiology	Btk<xid>/Btk<xid>	CBA/CaHN-Btk<xid>/J	N	15117762
MGI:3687743	F	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis	Btk<xid>/Btk<xid>	CBA/CaHN-Btk<xid>/J	N	15117762
MGI:3687743	F	MP:0001602	impaired myelopoiesis	Btk<xid>/Btk<xid>	CBA/CaHN-Btk<xid>/J	N	15117762
MGI:3687743	F	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality	Btk<xid>/Btk<xid>	CBA/CaHN-Btk<xid>/J	N	17998386
MGI:3687743	F	MP:0005087	decreased acute inflammation	Btk<xid>/Btk<xid>	CBA/CaHN-Btk<xid>/J	N	15117762
MGI:3687743	F	MP:0008174	decreased follicular B cell number	Btk<xid>/Btk<xid>	CBA/CaHN-Btk<xid>/J	N	11371362
MGI:3687743	F	MP:0000222	decreased neutrophil cell number	Btk<xid>/Btk<xid>	CBA/CaHN-Btk<xid>/J	N	15117762
MGI:3687750	M	MP:0005093	decreased B cell proliferation	Btk<xid>/Y	CBA/HN-Btk<xid>	N	805203
MGI:3687750	M	MP:0005017	decreased B cell number	Btk<xid>/Y	CBA/HN-Btk<xid>	N	805203
MGI:3687750	M	MP:0009339	decreased splenocyte number	Btk<xid>/Y	CBA/HN-Btk<xid>	N	805203
MGI:3687751	F	MP:0002459	abnormal B cell physiology	Btk<xid>/Btk<xid>	involves: CBA/HN * DBA/2N	N	805203
MGI:3687751	F	MP:0000694	spleen hypoplasia	Btk<xid>/Btk<xid>	involves: CBA/HN * DBA/2N	N	805203
MGI:3687751	F	MP:0005153	abnormal B cell proliferation	Btk<xid>/Btk<xid>	involves: CBA/HN * DBA/2N	N	805203
MGI:3687751	F	MP:0005017	decreased B cell number	Btk<xid>/Btk<xid>	involves: CBA/HN * DBA/2N	N	805203
MGI:3687752	M	MP:0005017	decreased B cell number	Btk<xid>/Y	involves: CBA/HN * DBA/2N	N	805203
MGI:3687752	M	MP:0005093	decreased B cell proliferation	Btk<xid>/Y	involves: CBA/HN * DBA/2N	N	805203
MGI:3687752	M	MP:0000694	spleen hypoplasia	Btk<xid>/Y	involves: CBA/HN * DBA/2N	N	805203
MGI:3687754	F	MP:0001844	autoimmune response	Btk<xid>/Btk<xid>	CBA/HN-Btk<xid>	N	17574818
MGI:3687754	F	MP:0009339	decreased splenocyte number	Btk<xid>/Btk<xid>	CBA/HN-Btk<xid>	N	805203
MGI:3687754	F	MP:0002403	abnormal pre-B cell morphology	Btk<xid>/Btk<xid>	CBA/HN-Btk<xid>	N	3875649
MGI:3687754	F	MP:0005093	decreased B cell proliferation	Btk<xid>/Btk<xid>	CBA/HN-Btk<xid>	N	805203
MGI:3687754	F	MP:0002401	abnormal lymphopoiesis	Btk<xid>/Btk<xid>	CBA/HN-Btk<xid>	N	3875649
MGI:3687754	F	MP:0000172	abnormal bone marrow cell number	Btk<xid>/Btk<xid>	CBA/HN-Btk<xid>	N	3875649
MGI:3687754	F	MP:0005017	decreased B cell number	Btk<xid>/Btk<xid>	CBA/HN-Btk<xid>	N	805203
MGI:3687955	F	MP:0010249	lactation failure	Stat5a<tm1Mam>/Stat5a<tm1Mam>	either: 129S6/SvEvTac-Stat5a<tm1Mam> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	9009201
MGI:3687955	F	MP:0006269	abnormal mammary gland growth during pregnancy	Stat5a<tm1Mam>/Stat5a<tm1Mam>	either: 129S6/SvEvTac-Stat5a<tm1Mam> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	9009201
MGI:3687955	F	MP:0000662	abnormal branching of the mammary ductal tree	Stat5a<tm1Mam>/Stat5a<tm1Mam>	either: 129S6/SvEvTac-Stat5a<tm1Mam> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	9009201
MGI:3687955	F	MP:0000628	abnormal mammary gland development	Stat5a<tm1Mam>/Stat5a<tm1Mam>	either: 129S6/SvEvTac-Stat5a<tm1Mam> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	9009201
MGI:3687955	F	MP:0006270	abnormal mammary gland growth during lactation	Stat5a<tm1Mam>/Stat5a<tm1Mam>	either: 129S6/SvEvTac-Stat5a<tm1Mam> or (involves: 129S6/SvEvTac * NIH Black Swiss)	N	9009201
MGI:3687963	M	MP:0003607	abnormal prostate gland physiology	Stat5a<tm1Mam>/Stat5a<tm1Mam>	involves: 129S6/SvEvTac	N	10908145
MGI:3687963	M	MP:0001168	abnormal prostate gland epithelium morphology	Stat5a<tm1Mam>/Stat5a<tm1Mam>	involves: 129S6/SvEvTac	N	10908145
MGI:3687963	M	MP:0009737	prostate gland cyst	Stat5a<tm1Mam>/Stat5a<tm1Mam>	involves: 129S6/SvEvTac	N	10908145
MGI:3688155	F	MP:0031422	failure of superovulation	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10342864
MGI:3688155	M	MP:0004933	abnormal epididymis epithelium morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	9393999
MGI:3688155	M	MP:0004933	abnormal epididymis epithelium morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10670526
MGI:3688155	F	MP:0001728	failure of embryo implantation	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	12297545
MGI:3688155	M	MP:0002687	oligozoospermia	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10670526
MGI:3688155	M	MP:0009205	abnormal internal male genitalia morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	8723431
MGI:3688155	F	MP:0008869	anovulation	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10919287
MGI:3688155	M	MP:0001146	abnormal testis morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10670526
MGI:3688155	M	MP:0001154	seminiferous tubule degeneration	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	8723431
MGI:3688155	M	MP:0001146	abnormal testis morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	8723431
MGI:3688155	M	MP:0002631	abnormal epididymis morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10670526
MGI:3688155	F	MP:0004905	decreased uterus weight	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	17495854
MGI:3688155	F	MP:0000628	abnormal mammary gland development	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10919287
MGI:3688155	F	MP:0004905	decreased uterus weight	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	11784006
MGI:3688155	M	MP:0011833	abnormal cremaster muscle morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	8723431
MGI:3688155	F	MP:0001129	impaired ovarian folliculogenesis	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10342864
MGI:3688155	F	MP:0001140	abnormal vagina epithelium morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	11784006
MGI:3688155	F	MP:0001134	absent corpus luteum	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10342864
MGI:3688155	F	MP:0001134	absent corpus luteum	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10919287
MGI:3688155	F	MP:0004834	ovary hemorrhage	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10919287
MGI:3688155	F	MP:0004834	ovary hemorrhage	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10342864
MGI:3688155	M	MP:0004728	abnormal efferent ductules of testis morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10670526
MGI:3688155	M	MP:0006423	dilated rete testis	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	9393999
MGI:3688155	F	MP:0001121	uterus hypoplasia	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	11784006
MGI:3688155	M	MP:0006423	dilated rete testis	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	11698654
MGI:3688155	M	MP:0003698	abnormal male reproductive system physiology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	9393999
MGI:3688155	M	MP:0009140	dilated efferent ductule of testis	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10670526
MGI:3688155	M	MP:0009140	dilated efferent ductule of testis	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	9393999
MGI:3688155	M	MP:0009140	dilated efferent ductule of testis	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	11698654
MGI:3688155	F	MP:0001126	abnormal ovary morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10919287
MGI:3688155	M	MP:0001925	male infertility	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	11698654
MGI:3688155	M	MP:0009824	spermatic granuloma	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10670526
MGI:3688155	M	MP:0004850	abnormal testis weight	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	9393999
MGI:3688155	F	MP:0009444	ovarian follicular cyst	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	11784006
MGI:3688155	F	MP:0009444	ovarian follicular cyst	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10919287
MGI:3688155	F	MP:0009444	ovarian follicular cyst	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	N	10342864
MGI:3688157	F	MP:0004905	decreased uterus weight	Vdr<tm1.1Gcm>/Vdr<tm1.1Gcm>	involves: 129S1/Sv * 129X1/SvJ	N	14584880
MGI:3688439	F	MP:0031434	increased miscarriage rate	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	N	9207075
MGI:3688439	F	MP:0013716	hypolactation	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	N	9207075
MGI:3688439	F	MP:0000628	abnormal mammary gland development	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	N	9207075
MGI:3688509	M	MP:0005584	abnormal enzyme/coenzyme activity	Slc16a2<tm1.1Sref>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	16709608
MGI:3688509	M	MP:0005474	increased triiodothyronine level	Slc16a2<tm1.1Sref>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	16709608
MGI:3688509	M	MP:0005473	decreased triiodothyronine level	Slc16a2<tm1.1Sref>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	16709608
MGI:3688509	M	MP:0005319	abnormal enzyme/coenzyme level	Slc16a2<tm1.1Sref>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	16709608
MGI:3688509	M	MP:0002968	increased circulating alkaline phosphatase level	Slc16a2<tm1.1Sref>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	16709608
MGI:3688509	M	MP:0005135	increased thyroid-stimulating hormone level	Slc16a2<tm1.1Sref>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	16709608
MGI:3688509	M	MP:0005476	abnormal circulating triiodothyronine level	Slc16a2<tm1.1Sref>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	16709608
MGI:3688509	M	MP:0005478	decreased circulating thyroxine level	Slc16a2<tm1.1Sref>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	16709608
MGI:3688509	M	MP:0005179	decreased circulating cholesterol level	Slc16a2<tm1.1Sref>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	16709608
MGI:3688509	M	MP:0005418	abnormal circulating hormone level	Slc16a2<tm1.1Sref>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	16709608
MGI:3688510	M	MP:0005474	increased triiodothyronine level	Slc16a2<tm1.1Sref>/Y	involves: 129/Sv * 129P2/OlaHsd	N	16709608
MGI:3688510	M	MP:0005418	abnormal circulating hormone level	Slc16a2<tm1.1Sref>/Y	involves: 129/Sv * 129P2/OlaHsd	N	16709608
MGI:3688510	M	MP:0005478	decreased circulating thyroxine level	Slc16a2<tm1.1Sref>/Y	involves: 129/Sv * 129P2/OlaHsd	N	16709608
MGI:3688511	F	MP:0005418	abnormal circulating hormone level	Slc16a2<tm1.1Sref>/Slc16a2<tm1.1Sref>	involves: 129P2/OlaHsd * C57BL/6J	N	16709608
MGI:3688511	F	MP:0005478	decreased circulating thyroxine level	Slc16a2<tm1.1Sref>/Slc16a2<tm1.1Sref>	involves: 129P2/OlaHsd * C57BL/6J	N	16709608
MGI:3688511	F	MP:0005474	increased triiodothyronine level	Slc16a2<tm1.1Sref>/Slc16a2<tm1.1Sref>	involves: 129P2/OlaHsd * C57BL/6J	N	16709608
MGI:3688515	M	MP:0011099	lethality throughout fetal growth and development, complete penetrance	Gata1<Plt13>/Y	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688515	M	MP:0001577	anemia	Gata1<Plt13>/Y	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688515	M	MP:0000601	small liver	Gata1<Plt13>/Y	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688515	M	MP:0001698	decreased embryo size	Gata1<Plt13>/Y	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688515	M	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Gata1<Plt13>/Y	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688515	M	MP:0013241	embryo tissue necrosis	Gata1<Plt13>/Y	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688516	F	MP:0000240	extramedullary hematopoiesis	Gata1<Plt13>/Gata1<+>	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688516	F	MP:0000691	enlarged spleen	Gata1<Plt13>/Gata1<+>	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688516	F	MP:0004025	polyploidy	Gata1<Plt13>/Gata1<+>	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688516	F	MP:0008254	increased megakaryocyte cell number	Gata1<Plt13>/Gata1<+>	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688516	F	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<Plt13>/Gata1<+>	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688516	F	MP:0001601	abnormal myelopoiesis	Gata1<Plt13>/Gata1<+>	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688516	F	MP:0002417	abnormal megakaryocyte morphology	Gata1<Plt13>/Gata1<+>	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688516	F	MP:0003179	thrombocytopenia	Gata1<Plt13>/Gata1<+>	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688516	F	MP:0004952	increased spleen weight	Gata1<Plt13>/Gata1<+>	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688516	F	MP:0000228	abnormal thrombopoiesis	Gata1<Plt13>/Gata1<+>	BALB/c-Gata1<Plt13>	N	16966598
MGI:3688530	M	MP:0005333	decreased heart rate	Ace2<tm1Cof>/Y	involves: 129S6/SvEvTac * C57BL/6J	N	16878172
MGI:3688530	M	MP:0006144	increased systemic arterial systolic blood pressure	Ace2<tm1Cof>/Y	involves: 129S6/SvEvTac * C57BL/6J	N	16878172
MGI:3688531	M	MP:0006144	increased systemic arterial systolic blood pressure	Ace2<tm1Cof>/Y	B6.129S6-Ace2<tm1Cof>	N	16878172
MGI:3688532	M	MP:0000231	hypertension	Ace2<tm1Cof>/Y	129S6/SvEvTac-Ace2<tm1Cof>	N	16878172
MGI:3688532	M	MP:0005385	cardiovascular system phenotype	Ace2<tm1Cof>/Y	129S6/SvEvTac-Ace2<tm1Cof>	Y	16878172
MGI:3688532	M	MP:0031232	increased circulating angiotensin II level	Ace2<tm1Cof>/Y	129S6/SvEvTac-Ace2<tm1Cof>	N	16878172
MGI:3688533	M	MP:0006126	abnormal cardiac outflow tract development	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688533	M	MP:0011099	lethality throughout fetal growth and development, complete penetrance	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688533	M	MP:0000284	double outlet right ventricle	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688533	M	MP:0003649	decreased heart right ventricle size	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688533	M	MP:0009886	failure of palatal shelf elevation	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688533	M	MP:0003052	omphalocele	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688533	M	MP:0010402	ventricular septal defect	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688533	M	MP:0000157	abnormal sternum morphology	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688533	M	MP:0010620	thick mitral valve	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688533	M	MP:0001785	edema	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688533	M	MP:0009890	cleft secondary palate	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688533	M	MP:0002633	persistent truncus arteriosus	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688533	M	MP:0010404	ostium primum atrial septal defect	Flna<Dilp2>/Y	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688534	F	MP:0000284	double outlet right ventricle	Flna<Dilp2>/Flna<+>	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688534	F	MP:0010402	ventricular septal defect	Flna<Dilp2>/Flna<+>	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688534	F	MP:0001319	irregularly shaped pupil	Flna<Dilp2>/Flna<+>	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688534	F	MP:0000157	abnormal sternum morphology	Flna<Dilp2>/Flna<+>	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688534	F	MP:0000159	abnormal xiphoid process morphology	Flna<Dilp2>/Flna<+>	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688534	F	MP:0009887	abnormal palatal shelf fusion at midline	Flna<Dilp2>/Flna<+>	involves: BALB/cAnN * C3H/HeN * C57BL/6	N	16825286
MGI:3688608	F	MP:0004292	abnormal spiral ligament fibrocyte morphology	Pou3f4<tm1Tno>/Pou3f4<tm1Tno>	involves: 129S4/SvJae * C57BL/6	N	10464101
MGI:3688608	F	MP:0001967	deafness	Pou3f4<tm1Tno>/Pou3f4<tm1Tno>	involves: 129S4/SvJae * C57BL/6	N	10464101
MGI:3688608	F	MP:0001967	deafness	Pou3f4<tm1Tno>/Pou3f4<tm1Tno>	involves: 129S4/SvJae * C57BL/6	N	12062767
MGI:3688608	F	MP:0005386	behavior/neurological phenotype	Pou3f4<tm1Tno>/Pou3f4<tm1Tno>	involves: 129S4/SvJae * C57BL/6	Y	10464101
MGI:3688608	F	MP:0000031	abnormal cochlea morphology	Pou3f4<tm1Tno>/Pou3f4<tm1Tno>	involves: 129S4/SvJae * C57BL/6	N	10464101
MGI:3688608	F	MP:0004411	decreased endocochlear potential	Pou3f4<tm1Tno>/Pou3f4<tm1Tno>	involves: 129S4/SvJae * C57BL/6	N	10464101
MGI:3688608	F	MP:0004294	abnormal type II spiral ligament fibrocytes	Pou3f4<tm1Tno>/Pou3f4<tm1Tno>	involves: 129S4/SvJae * C57BL/6	N	12062767
MGI:3688608	F	MP:0004294	abnormal type II spiral ligament fibrocytes	Pou3f4<tm1Tno>/Pou3f4<tm1Tno>	involves: 129S4/SvJae * C57BL/6	N	10464101
MGI:3688608	F	MP:0004293	abnormal type I spiral ligament fibrocytes	Pou3f4<tm1Tno>/Pou3f4<tm1Tno>	involves: 129S4/SvJae * C57BL/6	N	10464101
MGI:3688608	F	MP:0006023	detached Reissner membrane	Pou3f4<tm1Tno>/Pou3f4<tm1Tno>	involves: 129S4/SvJae * C57BL/6	N	12062767
MGI:3688608	F	MP:0011967	increased or absent threshold for auditory brainstem response	Pou3f4<tm1Tno>/Pou3f4<tm1Tno>	involves: 129S4/SvJae * C57BL/6	N	10464101
MGI:3688608	F	MP:0011967	increased or absent threshold for auditory brainstem response	Pou3f4<tm1Tno>/Pou3f4<tm1Tno>	involves: 129S4/SvJae * C57BL/6	N	12062767
MGI:3688625	F	MP:0006023	detached Reissner membrane	Pou3f4<tm1Tno>/Pou3f4<+>	involves: 129S4/SvJae * C57BL/6	N	12062767
MGI:3688625	F	MP:0004294	abnormal type II spiral ligament fibrocytes	Pou3f4<tm1Tno>/Pou3f4<+>	involves: 129S4/SvJae * C57BL/6	N	12062767
MGI:3688625	F	MP:0011967	increased or absent threshold for auditory brainstem response	Pou3f4<tm1Tno>/Pou3f4<+>	involves: 129S4/SvJae * C57BL/6	N	12062767
MGI:3688625	F	MP:0001967	deafness	Pou3f4<tm1Tno>/Pou3f4<+>	involves: 129S4/SvJae * C57BL/6	N	12062767
MGI:3688625	F	MP:0000031	abnormal cochlea morphology	Pou3f4<tm1Tno>/Pou3f4<+>	involves: 129S4/SvJae * C57BL/6	N	12062767
MGI:3688630	F	MP:0002206	abnormal CNS synaptic transmission	Nlgn1<tm1Bros>/Nlgn1<tm1Bros>,Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	Not Specified	N	16982420
MGI:3688630	F	MP:0001921	reduced fertility	Nlgn1<tm1Bros>/Nlgn1<tm1Bros>,Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	Not Specified	N	16982420
MGI:3688630	F	MP:0002068	abnormal parental behavior	Nlgn1<tm1Bros>/Nlgn1<tm1Bros>,Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	Not Specified	N	16982420
MGI:3688631	F	MP:0002206	abnormal CNS synaptic transmission	Nlgn2<tm1Bros>/Nlgn2<tm1Bros>,Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	Not Specified	N	16982420
MGI:3688631	F	MP:0001921	reduced fertility	Nlgn2<tm1Bros>/Nlgn2<tm1Bros>,Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	Not Specified	N	16982420
MGI:3688631	F	MP:0002068	abnormal parental behavior	Nlgn2<tm1Bros>/Nlgn2<tm1Bros>,Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	Not Specified	N	16982420
MGI:3688634	F	MP:0003861	abnormal nervous system development	Nlgn1<tm1Bros>/Nlgn1<tm1Bros>,Nlgn2<tm1Bros>/Nlgn2<tm1Bros>,Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	Not Specified	N	16982420
MGI:3688634	F	MP:0011087	neonatal lethality, complete penetrance	Nlgn1<tm1Bros>/Nlgn1<tm1Bros>,Nlgn2<tm1Bros>/Nlgn2<tm1Bros>,Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	Not Specified	N	16982420
MGI:3688634	F	MP:0001943	abnormal respiration	Nlgn1<tm1Bros>/Nlgn1<tm1Bros>,Nlgn2<tm1Bros>/Nlgn2<tm1Bros>,Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	Not Specified	N	16982420
MGI:3688634	F	MP:0010746	abnormal pre-Botzinger complex physiology	Nlgn1<tm1Bros>/Nlgn1<tm1Bros>,Nlgn2<tm1Bros>/Nlgn2<tm1Bros>,Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	Not Specified	N	16982420
MGI:3688634	F	MP:0001262	decreased body weight	Nlgn1<tm1Bros>/Nlgn1<tm1Bros>,Nlgn2<tm1Bros>/Nlgn2<tm1Bros>,Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	Not Specified	N	16982420
MGI:3688726	M	MP:0001922	reduced male fertility	Psip1<Gt(betageo)1Hgs>/Psip1<Gt(betageo)1Hgs>	B6.129P2-Psip1<Gt(betageo)1Hgs>	N	16980622
MGI:3688726	M	MP:0001147	small testis	Psip1<Gt(betageo)1Hgs>/Psip1<Gt(betageo)1Hgs>	B6.129P2-Psip1<Gt(betageo)1Hgs>	N	16980622
MGI:3688727	M	MP:0001922	reduced male fertility	Psip1<Gt(betageo)1Hgs>/Psip1<Gt(betageo)1Hgs>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * MF1)	N	16980622
MGI:3688727	M	MP:0001147	small testis	Psip1<Gt(betageo)1Hgs>/Psip1<Gt(betageo)1Hgs>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * MF1)	N	16980622
MGI:3688733	F	MP:0001382	abnormal nursing	Apc<tm2.1Rak>/Apc<+>	involves: 129/Sv * C57BL/6J * SJL	N	17002498
MGI:3688896	F	MP:0009659	striated fur	Strx2/Strx2<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3688896	F	MP:0001200	thick skin	Strx2/Strx2<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3688896	F	MP:0001192	scaly skin	Strx2/Strx2<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3688896	F	MP:0001265	decreased body size	Strx2/Strx2<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3688897	M	MP:0011091	prenatal lethality, complete penetrance	Strx2/Y	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3688905	F	MP:0001192	scaly skin	Strx3/Strx3<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3688905	F	MP:0009659	striated fur	Strx3/Strx3<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3688907	M	MP:0011091	prenatal lethality, complete penetrance	Strx3/Y	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3688915	F	MP:0009659	striated fur	Strx4/Strx4<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3688915	F	MP:0001192	scaly skin	Strx4/Strx4<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3688916	M	MP:0011091	prenatal lethality, complete penetrance	Strx4/Y	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689063	F	MP:0000421	mottled coat	Xmo2<1R>/Xmo2<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689063	F	MP:0001274	curly vibrissae	Xmo2<1R>/Xmo2<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689064	M	MP:0011091	prenatal lethality, complete penetrance	Xmo2<1R>/Y	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689065	M	MP:0011091	prenatal lethality, complete penetrance	Xmo3<1R>/Y	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689066	F	MP:0000421	mottled coat	Xmo3<1R>/Xmo3<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689066	F	MP:0001274	curly vibrissae	Xmo3<1R>/Xmo3<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689067	F	MP:0000421	mottled coat	Xmo4<1R>/Xmo4<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689067	F	MP:0001274	curly vibrissae	Xmo4<1R>/Xmo4<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689068	M	MP:0011085	postnatal lethality, complete penetrance	Xmo4<1R>/Y	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689068	M	MP:0002109	abnormal limb morphology	Xmo4<1R>/Y	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689068	M	MP:0000371	diluted coat color	Xmo4<1R>/Y	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689069	M	MP:0011091	prenatal lethality, complete penetrance	Xmo5<1R>/Y	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689070	F	MP:0001274	curly vibrissae	Xmo5<1R>/Xmo5<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689070	F	MP:0000421	mottled coat	Xmo5<1R>/Xmo5<+>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3689071	F	MP:0000421	mottled coat	Xmo6<1R>/Xmo6<+>	Not Specified	N	MGI:3588414
MGI:3689071	F	MP:0001274	curly vibrissae	Xmo6<1R>/Xmo6<+>	Not Specified	N	MGI:3588414
MGI:3689072	M	MP:0011091	prenatal lethality, complete penetrance	Xmo6<1R>/Y	Not Specified	N	MGI:3588414
MGI:3689112	F	MP:0001926	female infertility	fit5<1R>/fit5<1R>	R:D7R75M	N	MGI:3588414
MGI:3689112	M	MP:0001925	male infertility	fit5<1R>/fit5<1R>	R:D7R75M	N	MGI:3588414
MGI:3689112	M	MP:0004852	decreased testis weight	fit5<1R>/fit5<1R>	R:D7R75M	N	MGI:3588414
MGI:3689378	F	MP:0002637	small uterus	Cftr<tm1Kth>/Cftr<tm1Kth>	B6.129S7-Cftr<tm1Kth>	N	18325992
MGI:3689378	F	MP:0001135	abnormal uterine cervix morphology	Cftr<tm1Kth>/Cftr<tm1Kth>	B6.129S7-Cftr<tm1Kth>	N	18325992
MGI:3689378	F	MP:0001923	reduced female fertility	Cftr<tm1Kth>/Cftr<tm1Kth>	B6.129S7-Cftr<tm1Kth>	N	18325992
MGI:3689378	F	MP:0009081	thin uterus	Cftr<tm1Kth>/Cftr<tm1Kth>	B6.129S7-Cftr<tm1Kth>	N	18325992
MGI:3689378	F	MP:0001127	small ovary	Cftr<tm1Kth>/Cftr<tm1Kth>	B6.129S7-Cftr<tm1Kth>	N	18325992
MGI:3689378	F	MP:0004856	decreased ovary weight	Cftr<tm1Kth>/Cftr<tm1Kth>	B6.129S7-Cftr<tm1Kth>	N	18325992
MGI:3689378	M	MP:0031012	impaired sperm migration in female genital tract	Cftr<tm1Kth>/Cftr<tm1Kth>	B6.129S7-Cftr<tm1Kth>	N	18325992
MGI:3689378	F	MP:0003355	decreased ovulation rate	Cftr<tm1Kth>/Cftr<tm1Kth>	B6.129S7-Cftr<tm1Kth>	N	18325992
MGI:3689378	F	MP:0002680	decreased corpora lutea number	Cftr<tm1Kth>/Cftr<tm1Kth>	B6.129S7-Cftr<tm1Kth>	N	18325992
MGI:3689378	F	MP:0009009	absent estrous cycle	Cftr<tm1Kth>/Cftr<tm1Kth>	B6.129S7-Cftr<tm1Kth>	N	18325992
MGI:3689378	F	MP:0001938	delayed sexual maturation	Cftr<tm1Kth>/Cftr<tm1Kth>	B6.129S7-Cftr<tm1Kth>	N	18325992
MGI:3689378	F	MP:0009006	prolonged estrous cycle	Cftr<tm1Kth>/Cftr<tm1Kth>	B6.129S7-Cftr<tm1Kth>	N	18325992
MGI:3689378	F	MP:0004905	decreased uterus weight	Cftr<tm1Kth>/Cftr<tm1Kth>	B6.129S7-Cftr<tm1Kth>	N	18325992
MGI:3689509	F	MP:0003068	enlarged kidney	Adra1a<tm1Pcs>/Adra1a<tm1Pcs>,Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N	N	12782680
MGI:3689509	M	MP:0011952	decreased cardiac stroke volume	Adra1a<tm1Pcs>/Adra1a<tm1Pcs>,Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N	N	12782680
MGI:3689509	M	MP:0006138	congestive heart failure	Adra1a<tm1Pcs>/Adra1a<tm1Pcs>,Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N	N	12782680
MGI:3689509	M	MP:0012106	impaired exercise endurance	Adra1a<tm1Pcs>/Adra1a<tm1Pcs>,Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N	N	12782680
MGI:3689509	M	MP:0031635	increased heart left ventricle muscle contractility	Adra1a<tm1Pcs>/Adra1a<tm1Pcs>,Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N	N	12782680
MGI:3689509	M	MP:0003393	decreased cardiac output	Adra1a<tm1Pcs>/Adra1a<tm1Pcs>,Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N	N	12782680
MGI:3689509	M	MP:0002188	small heart	Adra1a<tm1Pcs>/Adra1a<tm1Pcs>,Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N	N	12782680
MGI:3689509	M	MP:0002834	decreased heart weight	Adra1a<tm1Pcs>/Adra1a<tm1Pcs>,Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N	N	12782680
MGI:3689509	M	MP:0004565	decreased myocardial fiber size	Adra1a<tm1Pcs>/Adra1a<tm1Pcs>,Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N	N	12782680
MGI:3689509	M	MP:0009763	increased susceptibility to induced morbidity/mortality	Adra1a<tm1Pcs>/Adra1a<tm1Pcs>,Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N	N	12782680
MGI:3689574	F	MP:0031422	failure of superovulation	Pgr<tm1.2Mlia>/Pgr<tm1.2Mlia>	involves: 129 * C57BL/6J	N	16868919
MGI:3689574	F	MP:0001926	female infertility	Pgr<tm1.2Mlia>/Pgr<tm1.2Mlia>	involves: 129 * C57BL/6J	N	16868919
MGI:3689583	F	MP:0031434	increased miscarriage rate	Mecom<Jbo>/Mecom<+>	C3N.C-Mecom<Jbo>	N	17029558
MGI:3689632	F	MP:0008301	adrenal medulla hyperplasia	Gt(ROSA)26Sor<tm1Fia>/Gt(ROSA)26Sor<+>,Hprt1<tm1(CMV-cre)Brd>/Hprt1<+>,Nf1<tm1Fcr>/Nf1<tm1Fcr>	involves: 129S/SvEv * 129S/SvEvBrd	N	16906226
MGI:3689632	F	MP:0000959	abnormal somatic sensory system morphology	Gt(ROSA)26Sor<tm1Fia>/Gt(ROSA)26Sor<+>,Hprt1<tm1(CMV-cre)Brd>/Hprt1<+>,Nf1<tm1Fcr>/Nf1<tm1Fcr>	involves: 129S/SvEv * 129S/SvEvBrd	N	16906226
MGI:3689632	F	MP:0000961	abnormal dorsal root ganglion morphology	Gt(ROSA)26Sor<tm1Fia>/Gt(ROSA)26Sor<+>,Hprt1<tm1(CMV-cre)Brd>/Hprt1<+>,Nf1<tm1Fcr>/Nf1<tm1Fcr>	involves: 129S/SvEv * 129S/SvEvBrd	N	16906226
MGI:3689632	F	MP:0001008	abnormal sympathetic ganglion morphology	Gt(ROSA)26Sor<tm1Fia>/Gt(ROSA)26Sor<+>,Hprt1<tm1(CMV-cre)Brd>/Hprt1<+>,Nf1<tm1Fcr>/Nf1<tm1Fcr>	involves: 129S/SvEv * 129S/SvEvBrd	N	16906226
MGI:3689632	F	MP:0011101	prenatal lethality, incomplete penetrance	Gt(ROSA)26Sor<tm1Fia>/Gt(ROSA)26Sor<+>,Hprt1<tm1(CMV-cre)Brd>/Hprt1<+>,Nf1<tm1Fcr>/Nf1<tm1Fcr>	involves: 129S/SvEv * 129S/SvEvBrd	N	16906226
MGI:3689632	F	MP:0005319	abnormal enzyme/coenzyme level	Gt(ROSA)26Sor<tm1Fia>/Gt(ROSA)26Sor<+>,Hprt1<tm1(CMV-cre)Brd>/Hprt1<+>,Nf1<tm1Fcr>/Nf1<tm1Fcr>	involves: 129S/SvEv * 129S/SvEvBrd	N	16906226
MGI:3689697	F	MP:0000959	abnormal somatic sensory system morphology	Gt(ROSA)26Sor<tm1Fia>/Gt(ROSA)26Sor<tm1Fia>,Hprt1<tm1(CMV-cre)Brd>/Hprt1<+>,Nf1<tm1Fcr>/Nf1<tm1Fcr>	involves: 129S/SvEv * 129S/SvEvBrd	N	16906226
MGI:3689720	F	MP:0001143	constricted vagina orifice	Lepr<db>/Lepr<db>	B6.Cg-Dock7<m> +/+ Lepr<db>/J	N	378276
MGI:3689720	F	MP:0008869	anovulation	Lepr<db>/Lepr<db>	B6.Cg-Dock7<m> +/+ Lepr<db>/J	N	12594516
MGI:3689720	M	MP:0001380	reduced male mating frequency	Lepr<db>/Lepr<db>	B6.Cg-Dock7<m> +/+ Lepr<db>/J	N	378276
MGI:3689720	F	MP:0001926	female infertility	Lepr<db>/Lepr<db>	B6.Cg-Dock7<m> +/+ Lepr<db>/J	N	378276
MGI:3689720	F	MP:0002637	small uterus	Lepr<db>/Lepr<db>	B6.Cg-Dock7<m> +/+ Lepr<db>/J	N	378276
MGI:3689720	F	MP:0009009	absent estrous cycle	Lepr<db>/Lepr<db>	B6.Cg-Dock7<m> +/+ Lepr<db>/J	N	378276
MGI:3689720	F	MP:0001926	female infertility	Lepr<db>/Lepr<db>	B6.Cg-Dock7<m> +/+ Lepr<db>/J	N	12594516
MGI:3689720	F	MP:0009021	absent estrus	Lepr<db>/Lepr<db>	B6.Cg-Dock7<m> +/+ Lepr<db>/J	N	12594516
MGI:3689720	F	MP:0001119	abnormal female reproductive system morphology	Lepr<db>/Lepr<db>	B6.Cg-Dock7<m> +/+ Lepr<db>/J	N	12594516
MGI:3689741	F	MP:0001386	abnormal maternal nurturing	S1pr2<tm1Jch>/S1pr2<tm1Jch>,S1pr3<tm1Jch>/S1pr3<tm1Jch>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	12006579
MGI:3690032	F	MP:0009506	abnormal mammary gland alveolus morphology	Erbb4<tm1Grl>/Erbb4<tm1Grl>,Tg(Myh6-ERBB4)HT2Gass/0	involves: 129S1/Sv * 129X1/SvJ	N	12824469
MGI:3690032	F	MP:0000628	abnormal mammary gland development	Erbb4<tm1Grl>/Erbb4<tm1Grl>,Tg(Myh6-ERBB4)HT2Gass/0	involves: 129S1/Sv * 129X1/SvJ	N	12824469
MGI:3690032	F	MP:0013716	hypolactation	Erbb4<tm1Grl>/Erbb4<tm1Grl>,Tg(Myh6-ERBB4)HT2Gass/0	involves: 129S1/Sv * 129X1/SvJ	N	12824469
MGI:3690032	F	MP:0006269	abnormal mammary gland growth during pregnancy	Erbb4<tm1Grl>/Erbb4<tm1Grl>,Tg(Myh6-ERBB4)HT2Gass/0	involves: 129S1/Sv * 129X1/SvJ	N	12824469
MGI:3690050	M	MP:0002216	abnormal seminiferous tubule morphology	Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>,Wt1<tm1Jae>/Wt1<tm2Vih>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * SJL	N	16877546
MGI:3690050	M	MP:0001147	small testis	Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>,Wt1<tm1Jae>/Wt1<tm2Vih>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * SJL	N	16877546
MGI:3690050	M	MP:0002786	abnormal Leydig cell morphology	Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>,Wt1<tm1Jae>/Wt1<tm2Vih>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * SJL	N	16877546
MGI:3690050	M	MP:0001146	abnormal testis morphology	Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>,Wt1<tm1Jae>/Wt1<tm2Vih>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * SJL	N	16877546
MGI:3690050	M	MP:0004109	abnormal Sertoli cell development	Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>,Wt1<tm1Jae>/Wt1<tm2Vih>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * SJL	N	16877546
MGI:3690050	M	MP:0001145	abnormal male reproductive system morphology	Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>,Wt1<tm1Jae>/Wt1<tm2Vih>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * SJL	N	16877546
MGI:3690050	M	MP:0001925	male infertility	Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>,Wt1<tm1Jae>/Wt1<tm2Vih>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * SJL	N	16877546
MGI:3690093	M	MP:0009454	impaired contextual conditioning behavior	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690093	M	MP:0008432	abnormal long-term spatial reference memory	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690093	M	MP:0020852	abnormal olfactory behavior	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690093	M	MP:0001394	circling	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690093	M	MP:0003462	abnormal response to novel odor	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690093	M	MP:0020395	abnormal response to social novelty	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690093	M	MP:0012307	impaired spatial learning	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690093	M	MP:0001363	increased anxiety-related response	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690093	M	MP:0001441	increased grooming behavior	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690093	M	MP:0002797	increased thigmotaxis	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690093	M	MP:0031391	increased locomotor activity	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690093	M	MP:0001360	abnormal social investigation	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690093	M	MP:0001447	abnormal nest building behavior	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690093	M	MP:0011622	abnormal habituation to a novel odor	Scn1a<tm1Wac>/Scn1a<+>	B6.129-Scn1a<tm1Wac>	N	22914087
MGI:3690366	M	MP:0004478	increased testicular teratoma incidence	Ptch1<tm1Mps>/Ptch1<+>,Ptch2<tm1Pmc>/Ptch2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16849540
MGI:3690429	F	MP:0001882	abnormal lactation	Plg<tm1Jld>/Plg<tm1Jld>	B6.129P2-Plg<tm1Jld>	N	11003846
MGI:3690429	F	MP:0001923	reduced female fertility	Plg<tm1Jld>/Plg<tm1Jld>	B6.129P2-Plg<tm1Jld>	N	11003846
MGI:3690449	M	MP:0004478	increased testicular teratoma incidence	Dnd1<Ter>/?	129S1/Sv-Kit<W> Oca2<p> Tyr<c-ch>	N	4692863
MGI:3690450	F	MP:0001127	small ovary	Dnd1<Ter>/Dnd1<Ter>	129S1/Sv-Kit<W> Oca2<p> Tyr<c-ch>	N	3860691
MGI:3690450	M	MP:0004852	decreased testis weight	Dnd1<Ter>/Dnd1<Ter>	129S1/Sv-Kit<W> Oca2<p> Tyr<c-ch>	N	3860691
MGI:3690450	M	MP:0004901	decreased male germ cell number	Dnd1<Ter>/Dnd1<Ter>	129S1/Sv-Kit<W> Oca2<p> Tyr<c-ch>	N	3860691
MGI:3690450	M	MP:0004478	increased testicular teratoma incidence	Dnd1<Ter>/Dnd1<Ter>	129S1/Sv-Kit<W> Oca2<p> Tyr<c-ch>	N	3860691
MGI:3690450	F	MP:0004856	decreased ovary weight	Dnd1<Ter>/Dnd1<Ter>	129S1/Sv-Kit<W> Oca2<p> Tyr<c-ch>	N	3860691
MGI:3690450	F	MP:0001126	abnormal ovary morphology	Dnd1<Ter>/Dnd1<Ter>	129S1/Sv-Kit<W> Oca2<p> Tyr<c-ch>	N	3860691
MGI:3690450	M	MP:0001147	small testis	Dnd1<Ter>/Dnd1<Ter>	129S1/Sv-Kit<W> Oca2<p> Tyr<c-ch>	N	3860691
MGI:3690450	F	MP:0005431	decreased oocyte number	Dnd1<Ter>/Dnd1<Ter>	129S1/Sv-Kit<W> Oca2<p> Tyr<c-ch>	N	3860691
MGI:3690450	M	MP:0001925	male infertility	Dnd1<Ter>/Dnd1<Ter>	129S1/Sv-Kit<W> Oca2<p> Tyr<c-ch>	N	3860691
MGI:3690451	M	MP:0004478	increased testicular teratoma incidence	Dnd1<Ter>/Dnd1<+>	129S1/Sv-Kit<W> Oca2<p> Tyr<c-ch>	N	3860691
MGI:3690452	M	MP:0004478	increased testicular teratoma incidence	Dnd1<Ter>/Dnd1<Ter>	involves: 129S1/Sv * C57BL/6	N	3860691
MGI:3690453	M	MP:0006262	increased testis tumor incidence	Dnd1<Ter>/Dnd1<+>	involves: 129S1/Sv * C57BL/6	N	3860691
MGI:3690453	M	MP:0001147	small testis	Dnd1<Ter>/Dnd1<+>	involves: 129S1/Sv * C57BL/6	N	3860691
MGI:3690453	F	MP:0001127	small ovary	Dnd1<Ter>/Dnd1<+>	involves: 129S1/Sv * C57BL/6	N	3860691
MGI:3690453	M	MP:0004478	increased testicular teratoma incidence	Dnd1<Ter>/Dnd1<+>	involves: 129S1/Sv * C57BL/6	N	3860691
MGI:3690623	F	MP:0001139	abnormal vagina morphology	Plg<tm1Jld>/Plg<tm1Jld>	involves: 129P2/OlaHsd * Black Swiss	N	8929539
MGI:3690647	M	MP:0004478	increased testicular teratoma incidence	Kitl<Sl>/Kitl<+>	involves: 129/Sv * C3H	N	MGI:1306770
MGI:3690850	M	MP:0000135	decreased compact bone thickness	Kitl<Sl>/Kitl<Sl-d>	(WC/ReJ Kitl<Sl> x B6.D2-Kitl<Sl-d>/J)F1-Kitl<Sl>/Kitl<Sl-d>/J	N	15765184
MGI:3690850	M	MP:0001262	decreased body weight	Kitl<Sl>/Kitl<Sl-d>	(WC/ReJ Kitl<Sl> x B6.D2-Kitl<Sl-d>/J)F1-Kitl<Sl>/Kitl<Sl-d>/J	N	15765184
MGI:3690850	M	MP:0001732	postnatal growth retardation	Kitl<Sl>/Kitl<Sl-d>	(WC/ReJ Kitl<Sl> x B6.D2-Kitl<Sl-d>/J)F1-Kitl<Sl>/Kitl<Sl-d>/J	N	15765184
MGI:3691029	F	MP:0001386	abnormal maternal nurturing	Adgrl1<tm1Sud>/Adgrl1<tm1Sud>	involves: 129S6/SvEvTac * C57BL/6	N	11741895
MGI:3691220	F	MP:0000662	abnormal branching of the mammary ductal tree	Nit1<tm1Hbn>/Nit1<tm1Hbn>,Tg(Wap-cre)11738Mam/0	involves: 129X1/SvJ * C57BL/6 * SJL	N	16864578
MGI:3691287	F	MP:0000662	abnormal branching of the mammary ductal tree	Erbb3<tm1Squ>/Erbb3<tm1Squ>,Tg(MMTV-cre)7Mul/0	involves: 129S6/SvEvTac * FVB/N	N	16991114
MGI:3691565	M	MP:0001922	reduced male fertility	Gba2<tm1Rus>/Gba2<tm1Rus>	involves: 129S6/SvEv * C57BL/6J	N	17080196
MGI:3691565	M	MP:0002687	oligozoospermia	Gba2<tm1Rus>/Gba2<tm1Rus>	involves: 129S6/SvEv * C57BL/6J	N	17080196
MGI:3691565	M	MP:0006362	abnormal male germ cell morphology	Gba2<tm1Rus>/Gba2<tm1Rus>	involves: 129S6/SvEv * C57BL/6J	N	17080196
MGI:3691565	M	MP:0002784	abnormal Sertoli cell morphology	Gba2<tm1Rus>/Gba2<tm1Rus>	involves: 129S6/SvEv * C57BL/6J	N	17080196
MGI:3691565	M	MP:0002686	globozoospermia	Gba2<tm1Rus>/Gba2<tm1Rus>	involves: 129S6/SvEv * C57BL/6J	N	17080196
MGI:3691565	M	MP:0009257	dilated seminiferous tubule	Gba2<tm1Rus>/Gba2<tm1Rus>	involves: 129S6/SvEv * C57BL/6J	N	17080196
MGI:3691565	M	MP:0001147	small testis	Gba2<tm1Rus>/Gba2<tm1Rus>	involves: 129S6/SvEv * C57BL/6J	N	17080196
MGI:3691594	M	MP:0001146	abnormal testis morphology	Akt2<tm1Hem>/Akt2<tm1Hem>,Akt3<tm1Hem>/Akt3<tm1Hem>	involves: 129P2/OlaHsd * C57BL/6	N	16923958
MGI:3691594	M	MP:0004852	decreased testis weight	Akt2<tm1Hem>/Akt2<tm1Hem>,Akt3<tm1Hem>/Akt3<tm1Hem>	involves: 129P2/OlaHsd * C57BL/6	N	16923958
MGI:3691682	F	MP:0000352	decreased cell proliferation	Fcs2<Pohnpei>/Fcs2<Pohnpei>	involves: C57BL/6J * Pohnpei	N	16842493
MGI:3691952	M	MP:0031629	abnormal mounting behavior	Del(6)1Mom/Del(6)1Mom	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	12214233
MGI:3692028	M	MP:0002675	asthenozoospermia	Hspa4l<tm1Imad>/Hspa4l<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	16923965
MGI:3692028	M	MP:0002687	oligozoospermia	Hspa4l<tm1Imad>/Hspa4l<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	16923965
MGI:3692028	M	MP:0004182	abnormal spermiation	Hspa4l<tm1Imad>/Hspa4l<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	16923965
MGI:3692028	M	MP:0001922	reduced male fertility	Hspa4l<tm1Imad>/Hspa4l<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	16923965
MGI:3692028	M	MP:0001156	abnormal spermatogenesis	Hspa4l<tm1Imad>/Hspa4l<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	16923965
MGI:3692029	M	MP:0001922	reduced male fertility	Hspa4l<tm1Imad>/Hspa4l<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ	N	16923965
MGI:3692109	F	MP:0001923	reduced female fertility	Plg<tm1Jld>/Plg<tm1Jld>	involves: 129P2/OlaHsd * Black Swiss * C57BL/6J	N	11003846
MGI:3692109	F	MP:0010249	lactation failure	Plg<tm1Jld>/Plg<tm1Jld>	involves: 129P2/OlaHsd * Black Swiss * C57BL/6J	N	11003846
MGI:3692109	F	MP:0000628	abnormal mammary gland development	Plg<tm1Jld>/Plg<tm1Jld>	involves: 129P2/OlaHsd * Black Swiss * C57BL/6J	N	11003846
MGI:3692109	F	MP:0006271	abnormal involution of the mammary gland	Plg<tm1Jld>/Plg<tm1Jld>	involves: 129P2/OlaHsd * Black Swiss * C57BL/6J	N	11003846
MGI:3692109	F	MP:0009507	abnormal mammary gland connective tissue morphology	Plg<tm1Jld>/Plg<tm1Jld>	involves: 129P2/OlaHsd * Black Swiss * C57BL/6J	N	11003846
MGI:3692109	F	MP:0006270	abnormal mammary gland growth during lactation	Plg<tm1Jld>/Plg<tm1Jld>	involves: 129P2/OlaHsd * Black Swiss * C57BL/6J	N	11003846
MGI:3692457	M	MP:0004542	impaired acrosome reaction	Taldo1<tm1Perl>/Taldo1<tm1Perl>	involves: 129S6/SvEvTac * C57BL/6	N	17003133
MGI:3692457	M	MP:0014465	abnormal sperm mitochondrial morphology	Taldo1<tm1Perl>/Taldo1<tm1Perl>	involves: 129S6/SvEvTac * C57BL/6	N	17003133
MGI:3692457	M	MP:0001925	male infertility	Taldo1<tm1Perl>/Taldo1<tm1Perl>	involves: 129S6/SvEvTac * C57BL/6	N	17003133
MGI:3692457	M	MP:0003698	abnormal male reproductive system physiology	Taldo1<tm1Perl>/Taldo1<tm1Perl>	involves: 129S6/SvEvTac * C57BL/6	N	17003133
MGI:3692457	M	MP:0002675	asthenozoospermia	Taldo1<tm1Perl>/Taldo1<tm1Perl>	involves: 129S6/SvEvTac * C57BL/6	N	17003133
MGI:3692457	M	MP:0004543	abnormal sperm physiology	Taldo1<tm1Perl>/Taldo1<tm1Perl>	involves: 129S6/SvEvTac * C57BL/6	N	17003133
MGI:3692523	M	MP:0001922	reduced male fertility	Taldo1<tm1Perl>/Taldo1<+>	involves: 129S6/SvEvTac * C57BL/6	N	17003133
MGI:3692523	M	MP:0004543	abnormal sperm physiology	Taldo1<tm1Perl>/Taldo1<+>	involves: 129S6/SvEvTac * C57BL/6	N	17003133
MGI:3692523	M	MP:0004542	impaired acrosome reaction	Taldo1<tm1Perl>/Taldo1<+>	involves: 129S6/SvEvTac * C57BL/6	N	17003133
MGI:3692580	M	MP:0000516	abnormal renal/urinary system morphology	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	N	10898794
MGI:3692580	M	MP:0001145	abnormal male reproductive system morphology	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	N	10898794
MGI:3692580	M	MP:0013320	dilated seminal vesicle	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	N	10898794
MGI:3692738	M	MP:0014052	increased male germ cell apoptosis	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17038506
MGI:3692738	M	MP:0005159	azoospermia	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17038506
MGI:3692738	M	MP:0001147	small testis	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17038506
MGI:3692738	F	MP:0001125	abnormal oocyte morphology	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17038506
MGI:3692738	M	MP:0001155	arrest of spermatogenesis	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17038506
MGI:3692738	M	MP:0006380	abnormal spermatid morphology	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17038506
MGI:3692738	M	MP:0006379	abnormal spermatocyte morphology	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17038506
MGI:3692738	M	MP:0001925	male infertility	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17038506
MGI:3692738	M	MP:0001156	abnormal spermatogenesis	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17038506
MGI:3692739	M	MP:0006379	abnormal spermatocyte morphology	Ddx4<tm1Tnc>/Ddx4<tm1Tnc>	involves: 129P2/OlaHsd * C57BL/6	N	17038506
MGI:3692739	M	MP:0008261	arrest of male meiosis	Ddx4<tm1Tnc>/Ddx4<tm1Tnc>	involves: 129P2/OlaHsd * C57BL/6	N	17038506
MGI:3692739	F	MP:0001125	abnormal oocyte morphology	Ddx4<tm1Tnc>/Ddx4<tm1Tnc>	involves: 129P2/OlaHsd * C57BL/6	N	17038506
MGI:3692885	M	MP:0001155	arrest of spermatogenesis	Stx2<repro34>/Stx2<repro34>	involves: C3HeB/FeJ * C57BL/6J	N	18277055
MGI:3692885	M	MP:0005159	azoospermia	Stx2<repro34>/Stx2<repro34>	involves: C3HeB/FeJ * C57BL/6J	N	18277055
MGI:3692885	M	MP:0005159	azoospermia	Stx2<repro34>/Stx2<repro34>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692885	M	MP:0008261	arrest of male meiosis	Stx2<repro34>/Stx2<repro34>	involves: C3HeB/FeJ * C57BL/6J	N	18277055
MGI:3692885	M	MP:0008261	arrest of male meiosis	Stx2<repro34>/Stx2<repro34>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692885	M	MP:0004852	decreased testis weight	Stx2<repro34>/Stx2<repro34>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692885	M	MP:0001147	small testis	Stx2<repro34>/Stx2<repro34>	involves: C3HeB/FeJ * C57BL/6J	N	18277055
MGI:3692885	M	MP:0020550	multinucleated giant male germ cells	Stx2<repro34>/Stx2<repro34>	involves: C3HeB/FeJ * C57BL/6J	N	18277055
MGI:3692885	M	MP:0001925	male infertility	Stx2<repro34>/Stx2<repro34>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692885	M	MP:0001925	male infertility	Stx2<repro34>/Stx2<repro34>	involves: C3HeB/FeJ * C57BL/6J	N	18277055
MGI:3692885	M	MP:0004910	decreased seminal vesicle weight	Stx2<repro34>/Stx2<repro34>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692891	M	MP:0005578	teratozoospermia	repro54/repro54	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692891	M	MP:0002687	oligozoospermia	repro54/repro54	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692891	M	MP:0001932	abnormal spermiogenesis	repro54/repro54	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692891	M	MP:0002675	asthenozoospermia	repro54/repro54	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692891	M	MP:0004910	decreased seminal vesicle weight	repro54/repro54	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692891	M	MP:0001925	male infertility	repro54/repro54	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692895	M	MP:0001156	abnormal spermatogenesis	repro30/repro30	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692895	M	MP:0005159	azoospermia	repro30/repro30	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692895	M	MP:0004910	decreased seminal vesicle weight	repro30/repro30	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692895	M	MP:0001925	male infertility	repro30/repro30	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692895	M	MP:0008261	arrest of male meiosis	repro30/repro30	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692899	M	MP:0004910	decreased seminal vesicle weight	repro48/repro48	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692899	M	MP:0001932	abnormal spermiogenesis	repro48/repro48	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692899	M	MP:0002687	oligozoospermia	repro48/repro48	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692899	M	MP:0001925	male infertility	repro48/repro48	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692903	M	MP:0002687	oligozoospermia	repro53/repro53	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692903	M	MP:0002675	asthenozoospermia	repro53/repro53	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692903	M	MP:0004910	decreased seminal vesicle weight	repro53/repro53	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692903	M	MP:0001925	male infertility	repro53/repro53	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692907	M	MP:0001925	male infertility	repro52/repro52	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692907	M	MP:0002687	oligozoospermia	repro52/repro52	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692907	M	MP:0004910	decreased seminal vesicle weight	repro52/repro52	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692907	M	MP:0002675	asthenozoospermia	repro52/repro52	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692910	M	MP:0004910	decreased seminal vesicle weight	repro51/repro51	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692910	M	MP:0005578	teratozoospermia	repro51/repro51	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692910	M	MP:0002687	oligozoospermia	repro51/repro51	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692910	M	MP:0002675	asthenozoospermia	repro51/repro51	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692910	M	MP:0001925	male infertility	repro51/repro51	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692914	M	MP:0000242	impaired fertilization	repro50/repro50	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692914	M	MP:0009230	abnormal sperm head morphology	repro50/repro50	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692914	M	MP:0001932	abnormal spermiogenesis	repro50/repro50	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692914	M	MP:0009239	short sperm flagellum	repro50/repro50	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692914	M	MP:0004910	decreased seminal vesicle weight	repro50/repro50	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692914	M	MP:0002687	oligozoospermia	repro50/repro50	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692914	M	MP:0020869	immotile sperm	repro50/repro50	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692914	M	MP:0005578	teratozoospermia	repro50/repro50	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692914	M	MP:0001925	male infertility	repro50/repro50	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692918	M	MP:0001932	abnormal spermiogenesis	repro49/repro49	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692918	M	MP:0005578	teratozoospermia	repro49/repro49	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692918	M	MP:0002675	asthenozoospermia	repro49/repro49	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692918	M	MP:0001156	abnormal spermatogenesis	repro49/repro49	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692918	M	MP:0002686	globozoospermia	repro49/repro49	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692918	M	MP:0004910	decreased seminal vesicle weight	repro49/repro49	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692918	M	MP:0001925	male infertility	repro49/repro49	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692922	M	MP:0001932	abnormal spermiogenesis	repro47/repro47	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692922	M	MP:0005578	teratozoospermia	repro47/repro47	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692922	M	MP:0004910	decreased seminal vesicle weight	repro47/repro47	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692922	M	MP:0002675	asthenozoospermia	repro47/repro47	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692922	M	MP:0001925	male infertility	repro47/repro47	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692922	M	MP:0002686	globozoospermia	repro47/repro47	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692922	M	MP:0001156	abnormal spermatogenesis	repro47/repro47	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3052828
MGI:3692934	F	MP:0000628	abnormal mammary gland development	Fkbp4<tm1Shou>/Fkbp4<tm1Shou>	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6J)	N	16873445
MGI:3692934	F	MP:0031420	decreased superovulation rate	Fkbp4<tm1Shou>/Fkbp4<tm1Shou>	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6J)	N	16873445
MGI:3692934	F	MP:0001926	female infertility	Fkbp4<tm1Shou>/Fkbp4<tm1Shou>	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6J)	N	16873445
MGI:3692934	F	MP:0003845	abnormal decidualization	Fkbp4<tm1Shou>/Fkbp4<tm1Shou>	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6J)	N	16873445
MGI:3693878	F	MP:0001926	female infertility	Kmt2c<tm1.1Jwle>/Kmt2c<tm1.1Jwle>	involves: 129S4/SvJae * 129X1/SvJ	N	17021013
MGI:3693878	F	MP:0001923	reduced female fertility	Kmt2c<tm1.1Jwle>/Kmt2c<tm1.1Jwle>	involves: 129S4/SvJae * 129X1/SvJ	N	17021013
MGI:3693878	M	MP:0001922	reduced male fertility	Kmt2c<tm1.1Jwle>/Kmt2c<tm1.1Jwle>	involves: 129S4/SvJae * 129X1/SvJ	N	17021013
MGI:3693951	M	MP:0002727	decreased circulating insulin level	Npy2r<tm1.1Hhz>/Npy2r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12072562
MGI:3693951	M	MP:0001783	decreased white adipose tissue amount	Npy2r<tm1.1Hhz>/Npy2r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12072562
MGI:3693951	M	MP:0008459	abnormal circulating pancreatic peptide level	Npy2r<tm1.1Hhz>/Npy2r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12072562
MGI:3693952	F	MP:0006269	abnormal mammary gland growth during pregnancy	Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3693952	M	MP:0008459	abnormal circulating pancreatic peptide level	Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694004	M	MP:0004852	decreased testis weight	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17210747
MGI:3694004	F	MP:0003572	abnormal uterus development	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17082261
MGI:3694004	M	MP:0003205	testicular atrophy	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17210747
MGI:3694004	F	MP:0008257	thin myometrium	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17082261
MGI:3694004	M	MP:0004727	absent epididymis	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17210747
MGI:3694004	M	MP:0004729	absent efferent ductules of testis	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17210747
MGI:3694004	F	MP:0009069	dilated oviduct	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17082261
MGI:3694004	M	MP:0002661	abnormal corpus epididymis morphology	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17210747
MGI:3694004	F	MP:0001926	female infertility	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17082261
MGI:3694004	F	MP:0001121	uterus hypoplasia	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17082261
MGI:3694004	F	MP:0001136	dilated uterine cervix	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17082261
MGI:3694004	M	MP:0001925	male infertility	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17210747
MGI:3694004	M	MP:0001155	arrest of spermatogenesis	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17210747
MGI:3694004	F	MP:0009215	absent uterine horn	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17082261
MGI:3694004	M	MP:0004930	small epididymis	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17210747
MGI:3694004	M	MP:0004933	abnormal epididymis epithelium morphology	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17210747
MGI:3694004	M	MP:0002660	abnormal caput epididymis morphology	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17210747
MGI:3694004	F	MP:0009224	absent endometrium	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17082261
MGI:3694004	F	MP:0001144	vagina atresia	Pax8<tm1Pgr>/Pax8<tm1Pgr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	17082261
MGI:3694008	F	MP:0000662	abnormal branching of the mammary ductal tree	Lep<ob>/Lep<ob>,Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694008	F	MP:0001142	abnormal vagina orifice morphology	Lep<ob>/Lep<ob>,Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694008	M	MP:0004909	increased seminal vesicle weight	Lep<ob>/Lep<ob>,Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694008	M	MP:0001152	increased Leydig cell number	Lep<ob>/Lep<ob>,Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694008	M	MP:0030603	increased sperm number	Lep<ob>/Lep<ob>,Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694008	F	MP:0001927	abnormal estrous cycle	Lep<ob>/Lep<ob>,Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694008	F	MP:0001131	abnormal ovarian follicle morphology	Lep<ob>/Lep<ob>,Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694010	F	MP:0009006	prolonged estrous cycle	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694010	F	MP:0001142	abnormal vagina orifice morphology	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694010	M	MP:0001925	male infertility	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694010	F	MP:0009017	prolonged estrus	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694010	M	MP:0004910	decreased seminal vesicle weight	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694010	M	MP:0004852	decreased testis weight	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12453895
MGI:3694010	M	MP:0004852	decreased testis weight	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694010	F	MP:0009011	prolonged diestrus	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694010	F	MP:0011125	decreased primary ovarian follicle number	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694010	F	MP:0000662	abnormal branching of the mammary ductal tree	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694010	F	MP:0001134	absent corpus luteum	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694010	F	MP:0031381	decreased secondary ovarian follicle number	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694010	F	MP:0001926	female infertility	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694010	M	MP:0001925	male infertility	Lep<ob>/Lep<ob>	involves: 129X1/SvJ * C57BL/6	N	12453895
MGI:3694012	F	MP:0001926	female infertility	Lep<ob>/Lep<ob>,Npy2r<tm1.1Hhz>/Npy2r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694012	M	MP:0001925	male infertility	Lep<ob>/Lep<ob>,Npy2r<tm1.1Hhz>/Npy2r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12000791
MGI:3694012	M	MP:0004852	decreased testis weight	Lep<ob>/Lep<ob>,Npy2r<tm1.1Hhz>/Npy2r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12453895
MGI:3694012	M	MP:0001925	male infertility	Lep<ob>/Lep<ob>,Npy2r<tm1.1Hhz>/Npy2r<tm1.1Hhz>	involves: 129X1/SvJ * C57BL/6	N	12453895
MGI:3694057	M	MP:0002631	abnormal epididymis morphology	Pdgfa<tm1Cbet>/Pdgfa<tm1Cbet>	involves: 129P2/OlaHsd * C57BL/6	N	14522834
MGI:3694057	M	MP:0001156	abnormal spermatogenesis	Pdgfa<tm1Cbet>/Pdgfa<tm1Cbet>	involves: 129P2/OlaHsd * C57BL/6	N	14522834
MGI:3694057	M	MP:0004933	abnormal epididymis epithelium morphology	Pdgfa<tm1Cbet>/Pdgfa<tm1Cbet>	involves: 129P2/OlaHsd * C57BL/6	N	14522834
MGI:3694057	M	MP:0001155	arrest of spermatogenesis	Pdgfa<tm1Cbet>/Pdgfa<tm1Cbet>	involves: 129P2/OlaHsd * C57BL/6	N	14522834
MGI:3694083	F	MP:0013716	hypolactation	Mfge8<tm1Osa>/Mfge8<tm1Osa>	B6.129-Mfge8<tm1Osa>	N	16275924
MGI:3694083	F	MP:0004047	abnormal milk composition	Mfge8<tm1Osa>/Mfge8<tm1Osa>	B6.129-Mfge8<tm1Osa>	N	16275924
MGI:3694083	F	MP:0006271	abnormal involution of the mammary gland	Mfge8<tm1Osa>/Mfge8<tm1Osa>	B6.129-Mfge8<tm1Osa>	N	16275924
MGI:3694083	F	MP:0006270	abnormal mammary gland growth during lactation	Mfge8<tm1Osa>/Mfge8<tm1Osa>	B6.129-Mfge8<tm1Osa>	N	16275924
MGI:3694207	F	MP:0012014	abnormal olfactory neuron innervation pattern	Cnga2<tm1Mom>/Cnga2<tm1Mom>,Or8a1<tm2Mom>/Or8a1<tm4Mom>	involves: 129P2/OlaHsd * C57BL/6	N	15186781
MGI:3694360	F	MP:0005431	decreased oocyte number	Ube3a<tm1Alb>/Ube3a<tm1Alb>	involves: 129S7/SvEvBrd * C57BL/6	N	11756548
MGI:3694360	F	MP:0001130	abnormal ovarian folliculogenesis	Ube3a<tm1Alb>/Ube3a<tm1Alb>	involves: 129S7/SvEvBrd * C57BL/6	N	11756548
MGI:3694360	F	MP:0006269	abnormal mammary gland growth during pregnancy	Ube3a<tm1Alb>/Ube3a<tm1Alb>	involves: 129S7/SvEvBrd * C57BL/6	N	11756548
MGI:3694360	M	MP:0004852	decreased testis weight	Ube3a<tm1Alb>/Ube3a<tm1Alb>	involves: 129S7/SvEvBrd * C57BL/6	N	11756548
MGI:3694360	M	MP:0001922	reduced male fertility	Ube3a<tm1Alb>/Ube3a<tm1Alb>	involves: 129S7/SvEvBrd * C57BL/6	N	11756548
MGI:3694360	M	MP:0003666	impaired sperm capacitation	Ube3a<tm1Alb>/Ube3a<tm1Alb>	involves: 129S7/SvEvBrd * C57BL/6	N	11756548
MGI:3694360	F	MP:0001923	reduced female fertility	Ube3a<tm1Alb>/Ube3a<tm1Alb>	involves: 129S7/SvEvBrd * C57BL/6	N	11756548
MGI:3694360	F	MP:0004856	decreased ovary weight	Ube3a<tm1Alb>/Ube3a<tm1Alb>	involves: 129S7/SvEvBrd * C57BL/6	N	11756548
MGI:3694360	F	MP:0004905	decreased uterus weight	Ube3a<tm1Alb>/Ube3a<tm1Alb>	involves: 129S7/SvEvBrd * C57BL/6	N	11756548
MGI:3694360	F	MP:0003356	impaired luteinization	Ube3a<tm1Alb>/Ube3a<tm1Alb>	involves: 129S7/SvEvBrd * C57BL/6	N	11756548
MGI:3694360	M	MP:0002687	oligozoospermia	Ube3a<tm1Alb>/Ube3a<tm1Alb>	involves: 129S7/SvEvBrd * C57BL/6	N	11756548
MGI:3694360	M	MP:0004962	decreased prostate gland weight	Ube3a<tm1Alb>/Ube3a<tm1Alb>	involves: 129S7/SvEvBrd * C57BL/6	N	11756548
MGI:3694473	M	MP:0004543	abnormal sperm physiology	Catsper3<tm1Clph>/Catsper3<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694473	M	MP:0005578	teratozoospermia	Catsper3<tm1Clph>/Catsper3<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694473	M	MP:0001925	male infertility	Catsper3<tm1Clph>/Catsper3<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694473	M	MP:0002674	abnormal sperm motility	Catsper3<tm1Clph>/Catsper3<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694473	M	MP:0002675	asthenozoospermia	Catsper3<tm1Clph>/Catsper3<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694473	M	MP:0003666	impaired sperm capacitation	Catsper3<tm1Clph>/Catsper3<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694474	M	MP:0002674	abnormal sperm motility	Catsper4<tm1Clph>/Catsper4<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694474	M	MP:0004543	abnormal sperm physiology	Catsper4<tm1Clph>/Catsper4<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694474	M	MP:0002675	asthenozoospermia	Catsper4<tm1Clph>/Catsper4<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694474	M	MP:0003666	impaired sperm capacitation	Catsper4<tm1Clph>/Catsper4<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694474	M	MP:0001925	male infertility	Catsper4<tm1Clph>/Catsper4<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694474	M	MP:0005578	teratozoospermia	Catsper4<tm1Clph>/Catsper4<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694475	M	MP:0002674	abnormal sperm motility	Catsper2<tm1Gar>/Catsper2<tm1Gar>	involves: 129S6/SvEvTac	N	17227845
MGI:3694475	M	MP:0002675	asthenozoospermia	Catsper2<tm1Gar>/Catsper2<tm1Gar>	involves: 129S6/SvEvTac	N	17227845
MGI:3694475	M	MP:0004543	abnormal sperm physiology	Catsper2<tm1Gar>/Catsper2<tm1Gar>	involves: 129S6/SvEvTac	N	17227845
MGI:3694476	M	MP:0002674	abnormal sperm motility	Catsper1<tm1Clph>/Catsper1<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694476	M	MP:0002675	asthenozoospermia	Catsper1<tm1Clph>/Catsper1<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694476	M	MP:0004543	abnormal sperm physiology	Catsper1<tm1Clph>/Catsper1<tm1Clph>	involves: 129S4/SvJae	N	17227845
MGI:3694476	M	MP:0005389	reproductive system phenotype	Catsper1<tm1Clph>/Catsper1<tm1Clph>	involves: 129S4/SvJae	Y	26429887
MGI:3694668	F	MP:0005597	decreased susceptibility to type I hypersensitivity reaction	Cysltr1<tm1Ykn>/Cysltr1<tm1Ykn>	involves: C57BL/6	N	11932261
MGI:3694668	F	MP:0002405	respiratory system inflammation	Cysltr1<tm1Ykn>/Cysltr1<tm1Ykn>	involves: C57BL/6	N	14970333
MGI:3694668	F	MP:0005621	abnormal cell physiology	Cysltr1<tm1Ykn>/Cysltr1<tm1Ykn>	involves: C57BL/6	N	11932261
MGI:3694668	F	MP:0003071	decreased vascular permeability	Cysltr1<tm1Ykn>/Cysltr1<tm1Ykn>	involves: C57BL/6	N	11932261
MGI:3694693	M	MP:0002843	decreased systemic arterial blood pressure	Cyp4a14<tm1Jhc>/Cyp4a14<tm1Jhc>	involves: 129S6/SvEvTac * 129X1/SvJ	N	11320253
MGI:3694693	M	MP:0006144	increased systemic arterial systolic blood pressure	Cyp4a14<tm1Jhc>/Cyp4a14<tm1Jhc>	involves: 129S6/SvEvTac * 129X1/SvJ	N	11320253
MGI:3694693	M	MP:0006143	increased systemic arterial diastolic blood pressure	Cyp4a14<tm1Jhc>/Cyp4a14<tm1Jhc>	involves: 129S6/SvEvTac * 129X1/SvJ	N	11320253
MGI:3694693	M	MP:0005531	increased renal vascular resistance	Cyp4a14<tm1Jhc>/Cyp4a14<tm1Jhc>	involves: 129S6/SvEvTac * 129X1/SvJ	N	11320253
MGI:3694762	M	MP:0003642	absent seminal vesicle	Pax2<tm1Mbu>/Pax2<tm1Mbu>	C3.129P2-Pax2<tm1Mbu>	N	10934015
MGI:3694762	M	MP:0004727	absent epididymis	Pax2<tm1Mbu>/Pax2<tm1Mbu>	C3.129P2-Pax2<tm1Mbu>	N	10934015
MGI:3694762	F	MP:0003575	absent oviduct	Pax2<tm1Mbu>/Pax2<tm1Mbu>	C3.129P2-Pax2<tm1Mbu>	N	10934015
MGI:3694762	M	MP:0003557	absent vas deferens	Pax2<tm1Mbu>/Pax2<tm1Mbu>	C3.129P2-Pax2<tm1Mbu>	N	10934015
MGI:3694762	F	MP:0003558	absent uterus	Pax2<tm1Mbu>/Pax2<tm1Mbu>	C3.129P2-Pax2<tm1Mbu>	N	10934015
MGI:3694762	F	MP:0003535	absent vagina	Pax2<tm1Mbu>/Pax2<tm1Mbu>	C3.129P2-Pax2<tm1Mbu>	N	10934015
MGI:3694964	F	MP:0003710	abnormal physiological neovascularization	Cxcr3<tm1Wwh>/Cxcr3<tm1Wwh>	B6.Cg-Cxcr3<tm1Wwh>	N	15718500
MGI:3694964	F	MP:0004751	increased length of allograft survival	Cxcr3<tm1Wwh>/Cxcr3<tm1Wwh>	B6.Cg-Cxcr3<tm1Wwh>	N	11085753
MGI:3694964	F	MP:0001861	lung inflammation	Cxcr3<tm1Wwh>/Cxcr3<tm1Wwh>	B6.Cg-Cxcr3<tm1Wwh>	N	15254596
MGI:3694964	F	MP:0031023	decreased susceptibility to Riboviria infection induced morbidity/mortality	Cxcr3<tm1Wwh>/Cxcr3<tm1Wwh>	B6.Cg-Cxcr3<tm1Wwh>	N	15152045
MGI:3694964	F	MP:0020914	decreased susceptibility to Riboviria infection	Cxcr3<tm1Wwh>/Cxcr3<tm1Wwh>	B6.Cg-Cxcr3<tm1Wwh>	N	15152045
MGI:3694964	F	MP:0009858	abnormal cellular extravasation	Cxcr3<tm1Wwh>/Cxcr3<tm1Wwh>	B6.Cg-Cxcr3<tm1Wwh>	N	15152045
MGI:3694964	F	MP:0009858	abnormal cellular extravasation	Cxcr3<tm1Wwh>/Cxcr3<tm1Wwh>	B6.Cg-Cxcr3<tm1Wwh>	N	15718500
MGI:3694964	F	MP:0003799	impaired macrophage chemotaxis	Cxcr3<tm1Wwh>/Cxcr3<tm1Wwh>	B6.Cg-Cxcr3<tm1Wwh>	N	15718500
MGI:3694964	F	MP:0003426	pulmonary interstitial fibrosis	Cxcr3<tm1Wwh>/Cxcr3<tm1Wwh>	B6.Cg-Cxcr3<tm1Wwh>	N	15254596
MGI:3694964	F	MP:0008750	abnormal interferon level	Cxcr3<tm1Wwh>/Cxcr3<tm1Wwh>	B6.Cg-Cxcr3<tm1Wwh>	N	15254596
MGI:3694965	M	MP:0001861	lung inflammation	Cxcr3<tm1Wwh>/Y	B6.Cg-Cxcr3<tm1Wwh>	N	15254596
MGI:3694965	M	MP:0004751	increased length of allograft survival	Cxcr3<tm1Wwh>/Y	B6.Cg-Cxcr3<tm1Wwh>	N	11085753
MGI:3694965	M	MP:0003426	pulmonary interstitial fibrosis	Cxcr3<tm1Wwh>/Y	B6.Cg-Cxcr3<tm1Wwh>	N	15254596
MGI:3694965	M	MP:0003799	impaired macrophage chemotaxis	Cxcr3<tm1Wwh>/Y	B6.Cg-Cxcr3<tm1Wwh>	N	15718500
MGI:3694965	M	MP:0009858	abnormal cellular extravasation	Cxcr3<tm1Wwh>/Y	B6.Cg-Cxcr3<tm1Wwh>	N	15718500
MGI:3694965	M	MP:0003710	abnormal physiological neovascularization	Cxcr3<tm1Wwh>/Y	B6.Cg-Cxcr3<tm1Wwh>	N	15718500
MGI:3694965	M	MP:0008750	abnormal interferon level	Cxcr3<tm1Wwh>/Y	B6.Cg-Cxcr3<tm1Wwh>	N	15254596
MGI:3694967	M	MP:0003721	increased tumor growth/size	Cxcr3<tm1Wwh>/Y,Tg(TRAMP)8247Ng/?	involves: C57BL/6	N	16941672
MGI:3694968	M	MP:0003447	decreased tumor growth/size	Cxcr2<tm1Mwm>/Cxcr2<tm1Mwm>,Tg(TRAMP)8247Ng/?	involves: 129S2/SvPas * BALB/c * C57BL/6	N	16941672
MGI:3695037	M	MP:0001922	reduced male fertility	Glrb<spa>/Glrb<spa>	Not Specified	N	MGI:61288
MGI:3695037	F	MP:0001386	abnormal maternal nurturing	Glrb<spa>/Glrb<spa>	Not Specified	N	MGI:61288
MGI:3695136	F	MP:0002637	small uterus	Trp63<tm1Fmc>/Trp63<+>	involves: 129S4/SvJae	N	12368184
MGI:3695136	F	MP:0001119	abnormal female reproductive system morphology	Trp63<tm1Fmc>/Trp63<+>	involves: 129S4/SvJae	N	12368184
MGI:3695277	M	MP:0004487	type I spiral ligament fibrocyte degeneration	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695277	M	MP:0002792	abnormal retina vasculature morphology	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695277	M	MP:0004758	absent strial marginal cells	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695277	M	MP:0001967	deafness	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695277	M	MP:0004748	increased susceptibility to age-related hearing loss	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695277	M	MP:0004404	cochlear outer hair cell degeneration	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695277	M	MP:0005386	behavior/neurological phenotype	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	Y	12040033
MGI:3695277	M	MP:0004368	abnormal stria vascularis vasculature morphology	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695277	M	MP:0004367	abnormal strial intermediate cell morphology	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695277	M	MP:0004363	stria vascularis degeneration	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695277	M	MP:0002857	cochlear ganglion degeneration	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695277	M	MP:0002855	abnormal cochlear ganglion morphology	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695277	M	MP:0004740	sensorineural hearing loss	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695277	M	MP:0004398	cochlear inner hair cell degeneration	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695277	M	MP:0011967	increased or absent threshold for auditory brainstem response	Ndp<tm1Wbrg>/Y	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	N	12040033
MGI:3695279	M	MP:0002286	cryptorchism	Parl<tm1.1Bdes>/Parl<tm1.1Bdes>	involves: 129P2/OlaHsd * C57BL/6J	N	16839884
MGI:3695279	M	MP:0001147	small testis	Parl<tm1.1Bdes>/Parl<tm1.1Bdes>	involves: 129P2/OlaHsd * C57BL/6J	N	16839884
MGI:3695279	M	MP:0004930	small epididymis	Parl<tm1.1Bdes>/Parl<tm1.1Bdes>	involves: 129P2/OlaHsd * C57BL/6J	N	16839884
MGI:3695279	F	MP:0004014	abnormal uterine environment	Parl<tm1.1Bdes>/Parl<tm1.1Bdes>	involves: 129P2/OlaHsd * C57BL/6J	N	16839884
MGI:3695279	M	MP:0001145	abnormal male reproductive system morphology	Parl<tm1.1Bdes>/Parl<tm1.1Bdes>	involves: 129P2/OlaHsd * C57BL/6J	N	16839884
MGI:3695413	M	MP:0001922	reduced male fertility	Sharpin<cpdm>/Sharpin<cpdm>	C57BL/KaLawRij-Sharpin<cpdm>	N	8774148
MGI:3695413	F	MP:0001926	female infertility	Sharpin<cpdm>/Sharpin<cpdm>	C57BL/KaLawRij-Sharpin<cpdm>	N	8362989
MGI:3695566	F	MP:0005450	abnormal energy expenditure	Agrp<tm1Sqn>/Agrp<tm1Sqn>	involves: 129S7/SvEvBrd * C57BL/6J	N	17097059
MGI:3695566	F	MP:0011939	increased food intake	Agrp<tm1Sqn>/Agrp<tm1Sqn>	involves: 129S7/SvEvBrd * C57BL/6J	N	17097059
MGI:3695566	M	MP:0001260	increased body weight	Agrp<tm1Sqn>/Agrp<tm1Sqn>	involves: 129S7/SvEvBrd * C57BL/6J	N	17097059
MGI:3695566	F	MP:0011049	impaired adaptive thermogenesis	Agrp<tm1Sqn>/Agrp<tm1Sqn>	involves: 129S7/SvEvBrd * C57BL/6J	N	17097059
MGI:3695566	F	MP:0003961	decreased lean body mass	Agrp<tm1Sqn>/Agrp<tm1Sqn>	involves: 129S7/SvEvBrd * C57BL/6J	N	17097059
MGI:3695722	M	MP:0011805	decreased cell migration	Nox1<tm1Cyn>/Y	involves: 129S1/Sv * 129X1/SvJ	N	23749776
MGI:3695722	M	MP:0003186	abnormal redox activity	Nox1<tm1Cyn>/Y	involves: 129S1/Sv * 129X1/SvJ	N	23749776
MGI:3695722	M	MP:0001792	impaired wound healing	Nox1<tm1Cyn>/Y	involves: 129S1/Sv * 129X1/SvJ	N	23749776
MGI:3695722	M	MP:0001613	abnormal vasodilation	Nox1<tm1Cyn>/Y	involves: 129S1/Sv * 129X1/SvJ	N	16246966
MGI:3695722	M	MP:0002843	decreased systemic arterial blood pressure	Nox1<tm1Cyn>/Y	involves: 129S1/Sv * 129X1/SvJ	N	16246966
MGI:3695722	M	MP:0003009	abnormal cytokine secretion	Nox1<tm1Cyn>/Y	involves: 129S1/Sv * 129X1/SvJ	N	23749776
MGI:3695921	F	MP:0002577	reduced enamel thickness	Amelx<tm1Msnd>/Amelx<tm1Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695921	F	MP:0002649	abnormal enamel rod pattern	Amelx<tm1Msnd>/Amelx<tm1Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695921	F	MP:0002576	abnormal enamel morphology	Amelx<tm1Msnd>/Amelx<tm1Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695921	F	MP:0030458	abnormal tooth wear	Amelx<tm1Msnd>/Amelx<tm1Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695921	F	MP:0030457	abnormal molar cusp morphology	Amelx<tm1Msnd>/Amelx<tm1Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695921	F	MP:0002650	abnormal ameloblast morphology	Amelx<tm1Msnd>/Amelx<tm1Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695921	F	MP:0000126	brittle teeth	Amelx<tm1Msnd>/Amelx<tm1Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695921	F	MP:0030513	short Tomes' process	Amelx<tm1Msnd>/Amelx<tm1Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695922	F	MP:0002649	abnormal enamel rod pattern	Amelx<tm1Msnd>/Amelx<+>	involves: 129X1/SvJ	N	16707492
MGI:3695922	F	MP:0000126	brittle teeth	Amelx<tm1Msnd>/Amelx<+>	involves: 129X1/SvJ	N	16707492
MGI:3695923	F	MP:0003932	abnormal molar crown morphology	Amelx<tm2Msnd>/Amelx<tm2Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695923	F	MP:0002577	reduced enamel thickness	Amelx<tm2Msnd>/Amelx<tm2Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695923	F	MP:0030513	short Tomes' process	Amelx<tm2Msnd>/Amelx<tm2Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695923	F	MP:0002649	abnormal enamel rod pattern	Amelx<tm2Msnd>/Amelx<tm2Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695923	F	MP:0030458	abnormal tooth wear	Amelx<tm2Msnd>/Amelx<tm2Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695923	F	MP:0002576	abnormal enamel morphology	Amelx<tm2Msnd>/Amelx<tm2Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695923	F	MP:0002650	abnormal ameloblast morphology	Amelx<tm2Msnd>/Amelx<tm2Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695923	F	MP:0000126	brittle teeth	Amelx<tm2Msnd>/Amelx<tm2Msnd>	involves: 129X1/SvJ	N	16707492
MGI:3695924	F	MP:0000126	brittle teeth	Amelx<tm2Msnd>/Amelx<+>	involves: 129X1/SvJ	N	16707492
MGI:3695924	F	MP:0002649	abnormal enamel rod pattern	Amelx<tm2Msnd>/Amelx<+>	involves: 129X1/SvJ	N	16707492
MGI:3696039	F	MP:0001386	abnormal maternal nurturing	Fign<fi>/Fign<fi>	mixed	N	MGI:61244
MGI:3696354	M	MP:0001146	abnormal testis morphology	Ercc2<tm3Jhjh>/Ercc2<tm3Jhjh>	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	16904611
MGI:3696370	F	MP:0001386	abnormal maternal nurturing	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16362077
MGI:3696370	M	MP:0001925	male infertility	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16362077
MGI:3696388	M	MP:0001154	seminiferous tubule degeneration	Ybx3<tm1Ley>/Ybx3<tm1Ley>	involves: 129X1/SvJ * C57BL/6	N	16954378
MGI:3696388	M	MP:0001156	abnormal spermatogenesis	Ybx3<tm1Ley>/Ybx3<tm1Ley>	involves: 129X1/SvJ * C57BL/6	N	16954378
MGI:3696388	M	MP:0002687	oligozoospermia	Ybx3<tm1Ley>/Ybx3<tm1Ley>	involves: 129X1/SvJ * C57BL/6	N	16954378
MGI:3696388	M	MP:0001147	small testis	Ybx3<tm1Ley>/Ybx3<tm1Ley>	involves: 129X1/SvJ * C57BL/6	N	16954378
MGI:3696388	M	MP:0001925	male infertility	Ybx3<tm1Ley>/Ybx3<tm1Ley>	involves: 129X1/SvJ * C57BL/6	N	16954378
MGI:3696452	M	MP:0001354	increased aggression towards male mice	Imab<NZB/BlNJ>/?	involves: CBA/H * NZB/BlNJ	N	8138160
MGI:3696558	M	MP:0003415	priapism	Serpinc1<tm1Dwr>/Serpinc1<tm1Dwr>	involves: 129S1/Sv * 129X1/SvJ	N	14592998
MGI:3696558	M	MP:0005187	abnormal penis morphology	Serpinc1<tm1Dwr>/Serpinc1<tm1Dwr>	involves: 129S1/Sv * 129X1/SvJ	N	14592998
MGI:3696685	F	MP:0004047	abnormal milk composition	Csn2<tm1Psim>/Csn2<tm1Psim>	involves: 129P2/OlaHsd * MF1	N	8016126
MGI:3696695	F	MP:0001126	abnormal ovary morphology	Brca1<tm1Brn>/Brca1<tm1Brn>	involves: 129P2/OlaHsd	N	17070800
MGI:3696789	F	MP:0001386	abnormal maternal nurturing	Mcoln3<Va>/Mcoln3<+>	involves: C57BL * C57BR	N	MGI:61341
MGI:3696790	F	MP:0001386	abnormal maternal nurturing	Mcoln3<Va>/Mcoln3<Va>	involves: C57BL * C57BR	N	MGI:61341
MGI:3696841	M	MP:0001922	reduced male fertility	Csf1r<tm1Ers>/Csf1r<tm1Ers>	involves: 129X1/SvJ * C3Heb/FeJ * C57BL/6J	N	11756160
MGI:3696841	F	MP:0009006	prolonged estrous cycle	Csf1r<tm1Ers>/Csf1r<tm1Ers>	involves: 129X1/SvJ * C3Heb/FeJ * C57BL/6J	N	11756160
MGI:3696841	M	MP:0002566	abnormal sexual interaction	Csf1r<tm1Ers>/Csf1r<tm1Ers>	involves: 129X1/SvJ * C3Heb/FeJ * C57BL/6J	N	11756160
MGI:3696841	F	MP:0009011	prolonged diestrus	Csf1r<tm1Ers>/Csf1r<tm1Ers>	involves: 129X1/SvJ * C3Heb/FeJ * C57BL/6J	N	11756160
MGI:3696841	M	MP:0002687	oligozoospermia	Csf1r<tm1Ers>/Csf1r<tm1Ers>	involves: 129X1/SvJ * C3Heb/FeJ * C57BL/6J	N	11756160
MGI:3696841	M	MP:0014269	decreased testes secretion	Csf1r<tm1Ers>/Csf1r<tm1Ers>	involves: 129X1/SvJ * C3Heb/FeJ * C57BL/6J	N	11756160
MGI:3696841	F	MP:0006269	abnormal mammary gland growth during pregnancy	Csf1r<tm1Ers>/Csf1r<tm1Ers>	involves: 129X1/SvJ * C3Heb/FeJ * C57BL/6J	N	11756160
MGI:3696844	M	MP:0001156	abnormal spermatogenesis	Cib1<tm1Prse>/Cib1<tm1Prse>	involves: 129S6/SvEvTac * C57BL/6	N	16982698
MGI:3696844	M	MP:0004852	decreased testis weight	Cib1<tm1Prse>/Cib1<tm1Prse>	involves: 129S6/SvEvTac * C57BL/6	N	16982698
MGI:3696844	M	MP:0001932	abnormal spermiogenesis	Cib1<tm1Prse>/Cib1<tm1Prse>	involves: 129S6/SvEvTac * C57BL/6	N	16982698
MGI:3696844	M	MP:0001925	male infertility	Cib1<tm1Prse>/Cib1<tm1Prse>	involves: 129S6/SvEvTac * C57BL/6	N	16982698
MGI:3696844	M	MP:0001155	arrest of spermatogenesis	Cib1<tm1Prse>/Cib1<tm1Prse>	involves: 129S6/SvEvTac * C57BL/6	N	16982698
MGI:3696844	M	MP:0005159	azoospermia	Cib1<tm1Prse>/Cib1<tm1Prse>	involves: 129S6/SvEvTac * C57BL/6	N	16982698
MGI:3696855	M	MP:0002161	abnormal fertility/fecundity	Lmx1a<dr-10J>/Lmx1a<dr-10J>	129P3/J-Lmx1a<dr-10J>/J	N	MGI:3767316
MGI:3696941	M	MP:0003830	abnormal testis development	Acvr2a<tm1Hsch>/Acvr2a<tm1Hsch>	involves: 129S1/Sv * C57BL/6J	N	10452853
MGI:3696941	F	MP:0001923	reduced female fertility	Acvr2a<tm1Hsch>/Acvr2a<tm1Hsch>	involves: 129S1/Sv * C57BL/6J	N	10452853
MGI:3696950	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Atrx<tm1Rjg>/Y,Tg(Gata1-cre)1Sho/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16628246
MGI:3696950	M	MP:0002582	disorganized extraembryonic tissue	Atrx<tm1Rjg>/Y,Tg(Gata1-cre)1Sho/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16628246
MGI:3696950	M	MP:0003984	embryonic growth retardation	Atrx<tm1Rjg>/Y,Tg(Gata1-cre)1Sho/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16628246
MGI:3696950	M	MP:0005032	abnormal ectoplacental cone morphology	Atrx<tm1Rjg>/Y,Tg(Gata1-cre)1Sho/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16628246
MGI:3696950	M	MP:0005028	abnormal trophectoderm morphology	Atrx<tm1Rjg>/Y,Tg(Gata1-cre)1Sho/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16628246
MGI:3696950	M	MP:0000352	decreased cell proliferation	Atrx<tm1Rjg>/Y,Tg(Gata1-cre)1Sho/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16628246
MGI:3696950	M	MP:0002584	small ectoplacental cone	Atrx<tm1Rjg>/Y,Tg(Gata1-cre)1Sho/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16628246
MGI:3696950	M	MP:0001698	decreased embryo size	Atrx<tm1Rjg>/Y,Tg(Gata1-cre)1Sho/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16628246
MGI:3696950	M	MP:0001713	decreased trophoblast giant cell number	Atrx<tm1Rjg>/Y,Tg(Gata1-cre)1Sho/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16628246
MGI:3696951	F	MP:0001919	abnormal reproductive system physiology	Atrx<tm1Rjg>/Atrx<+>,Tg(Gata1-cre)1Sho/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16628246
MGI:3696951	F	MP:0003787	abnormal imprinting	Atrx<tm1Rjg>/Atrx<+>,Tg(Gata1-cre)1Sho/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16628246
MGI:3696951	F	MP:0004924	abnormal behavior	Atrx<tm1Rjg>/Atrx<+>,Tg(Gata1-cre)1Sho/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16628246
MGI:3696951	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Atrx<tm1Rjg>/Atrx<+>,Tg(Gata1-cre)1Sho/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16628246
MGI:3697461	F	MP:0009733	absent nipple	Gata3<tm3Gsv>/Gata3<tm3Gsv>,Tg(KRT14-cre)8Brn/0	involves: 129P2/OlaHsd * FVB/N	N	17151017
MGI:3697465	F	MP:0001764	abnormal homeostasis	Cltrn<tm1.1Pngr>/Cltrn<tm1.1Pngr>	involves: 129P2/OlaHsd * C57BL/6J	N	17167413
MGI:3697465	F	MP:0011417	abnormal renal transport	Cltrn<tm1.1Pngr>/Cltrn<tm1.1Pngr>	involves: 129P2/OlaHsd * C57BL/6J	N	17167413
MGI:3697465	F	MP:0008055	increased urine osmolality	Cltrn<tm1.1Pngr>/Cltrn<tm1.1Pngr>	involves: 129P2/OlaHsd * C57BL/6J	N	17167413
MGI:3697465	F	MP:0001762	polyuria	Cltrn<tm1.1Pngr>/Cltrn<tm1.1Pngr>	involves: 129P2/OlaHsd * C57BL/6J	N	17167413
MGI:3697468	M	MP:0001922	reduced male fertility	Oca2<p-bs>/Oca2<p-bs>	Not Specified	N	MGI:63221
MGI:3697468	M	MP:0001932	abnormal spermiogenesis	Oca2<p-bs>/Oca2<p-bs>	Not Specified	N	MGI:63221
MGI:3697515	F	MP:0002169	no abnormal phenotype detected	Foxp3<tm1Tch>/Foxp3<+>	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0008721	abnormal chemokine level	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0001577	anemia	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0005011	increased eosinophil cell number	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0002497	increased IgE level	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0003945	abnormal lymphocyte physiology	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0008074	increased CD4-positive, alpha-beta T cell number	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0008078	increased CD8-positive, alpha-beta T cell number	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0008553	increased circulating tumor necrosis factor level	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0004975	absent regulatory T cells	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0000218	increased leukocyte cell number	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0003179	thrombocytopenia	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0008577	increased circulating interferon-gamma level	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0000691	enlarged spleen	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0008593	increased circulating interleukin-10 level	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0008596	increased circulating interleukin-6 level	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0008499	increased IgG1 level	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0008602	increased circulating interleukin-4 level	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0008626	increased circulating interleukin-5 level	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0002281	abnormal respiratory mucosa goblet cell morphology	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0001845	abnormal inflammatory response	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0001194	dermatitis	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0002405	respiratory system inflammation	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0011085	postnatal lethality, complete penetrance	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	17273171
MGI:3697516	M	MP:0011085	postnatal lethality, complete penetrance	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0003009	abnormal cytokine secretion	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0000491	crypts of Lieberkuhn abscesses	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0005013	increased lymphocyte cell number	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0001829	increased activated T cell number	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697516	M	MP:0000220	increased monocyte cell number	Foxp3<tm1Tch>/Y	C.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697517	M	MP:0000220	increased monocyte cell number	Foxp3<tm1Tch>/Y	B6.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697517	M	MP:0011085	postnatal lethality, complete penetrance	Foxp3<tm1Tch>/Y	B6.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697517	M	MP:0001845	abnormal inflammatory response	Foxp3<tm1Tch>/Y	B6.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697517	M	MP:0002497	increased IgE level	Foxp3<tm1Tch>/Y	B6.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697517	M	MP:0000218	increased leukocyte cell number	Foxp3<tm1Tch>/Y	B6.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697517	M	MP:0005011	increased eosinophil cell number	Foxp3<tm1Tch>/Y	B6.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697517	M	MP:0001577	anemia	Foxp3<tm1Tch>/Y	B6.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697517	M	MP:0001194	dermatitis	Foxp3<tm1Tch>/Y	B6.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697517	M	MP:0003179	thrombocytopenia	Foxp3<tm1Tch>/Y	B6.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697517	M	MP:0002405	respiratory system inflammation	Foxp3<tm1Tch>/Y	B6.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697517	M	MP:0005013	increased lymphocyte cell number	Foxp3<tm1Tch>/Y	B6.129X1-Foxp3<tm1Tch>	N	16275384
MGI:3697518	M	MP:0003009	abnormal cytokine secretion	Foxp3<tm1Tch>/Y,Stat6<tm1Gru>/Stat6<tm1Gru>	C.129-Stat6<tm1Gru> Foxp3<tm1Tch>	N	16275384
MGI:3697518	M	MP:0005011	increased eosinophil cell number	Foxp3<tm1Tch>/Y,Stat6<tm1Gru>/Stat6<tm1Gru>	C.129-Stat6<tm1Gru> Foxp3<tm1Tch>	N	16275384
MGI:3697518	M	MP:0011083	lethality at weaning, complete penetrance	Foxp3<tm1Tch>/Y,Stat6<tm1Gru>/Stat6<tm1Gru>	C.129-Stat6<tm1Gru> Foxp3<tm1Tch>	N	16275384
MGI:3697518	M	MP:0005387	immune system phenotype	Foxp3<tm1Tch>/Y,Stat6<tm1Gru>/Stat6<tm1Gru>	C.129-Stat6<tm1Gru> Foxp3<tm1Tch>	Y	16275384
MGI:3697518	M	MP:0005388	respiratory system phenotype	Foxp3<tm1Tch>/Y,Stat6<tm1Gru>/Stat6<tm1Gru>	C.129-Stat6<tm1Gru> Foxp3<tm1Tch>	Y	16275384
MGI:3697518	M	MP:0008577	increased circulating interferon-gamma level	Foxp3<tm1Tch>/Y,Stat6<tm1Gru>/Stat6<tm1Gru>	C.129-Stat6<tm1Gru> Foxp3<tm1Tch>	N	16275384
MGI:3697584	F	MP:0006269	abnormal mammary gland growth during pregnancy	Cdh1<tm1Kem>/Cdh1<tm2Kem>,Tg(MMTV-cre)1Kem/0	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6	N	12049767
MGI:3697584	F	MP:0006270	abnormal mammary gland growth during lactation	Cdh1<tm1Kem>/Cdh1<tm2Kem>,Tg(MMTV-cre)1Kem/0	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6	N	12049767
MGI:3697584	F	MP:0010249	lactation failure	Cdh1<tm1Kem>/Cdh1<tm2Kem>,Tg(MMTV-cre)1Kem/0	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6	N	12049767
MGI:3697584	F	MP:0004047	abnormal milk composition	Cdh1<tm1Kem>/Cdh1<tm2Kem>,Tg(MMTV-cre)1Kem/0	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6	N	12049767
MGI:3697585	F	MP:0004256	abnormal maternal decidual layer morphology	Cr1l<tm1Hmo>/Cr1l<tm1Hmo>	involves: 129X1/SvJ	N	10642554
MGI:3697678	F	MP:0001926	female infertility	Scarb1<tm1.1Thh>/Scarb1<tm1.1Thh>	B6.129X1-Scarb1<tm1.1Thh>	N	16964311
MGI:3697681	F	MP:0002294	short gestation period	Comt<tm1Kara>/Comt<tm1Kara>	involves: 129S4/SvJaeSor	N	18469803
MGI:3697681	F	MP:0004256	abnormal maternal decidual layer morphology	Comt<tm1Kara>/Comt<tm1Kara>	involves: 129S4/SvJaeSor	N	18469803
MGI:3697681	F	MP:0009394	increased uterine NK cell number	Comt<tm1Kara>/Comt<tm1Kara>	involves: 129S4/SvJaeSor	N	18469803
MGI:3697681	F	MP:0009661	abnormal pregnancy	Comt<tm1Kara>/Comt<tm1Kara>	involves: 129S4/SvJaeSor	N	18469803
MGI:3697904	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm1Isrd>/Y	involves: C57BL/6	N	17056592
MGI:3697912	M	MP:0002687	oligozoospermia	repro2/repro2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697912	M	MP:0030590	abnormal sperm fibrous sheath morphology	repro2/repro2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697912	M	MP:0001925	male infertility	repro2/repro2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697912	M	MP:0009232	abnormal sperm nucleus morphology	repro2/repro2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697912	M	MP:0006380	abnormal spermatid morphology	repro2/repro2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697912	M	MP:0009238	coiled sperm flagellum	repro2/repro2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697912	M	MP:0020869	immotile sperm	repro2/repro2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697912	M	MP:0005578	teratozoospermia	repro2/repro2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697912	M	MP:0009239	short sperm flagellum	repro2/repro2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697912	M	MP:0009234	absent sperm head	repro2/repro2	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697913	M	MP:0009833	absent sperm mitochondrial sheath	repro3/repro3	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697913	M	MP:0001925	male infertility	repro3/repro3	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697913	M	MP:0020869	immotile sperm	repro3/repro3	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697913	M	MP:0006380	abnormal spermatid morphology	repro3/repro3	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697913	M	MP:0009239	short sperm flagellum	repro3/repro3	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697913	M	MP:0008892	abnormal sperm flagellum morphology	repro3/repro3	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697913	M	MP:0002687	oligozoospermia	repro3/repro3	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697913	M	MP:0009232	abnormal sperm nucleus morphology	repro3/repro3	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697913	M	MP:0005578	teratozoospermia	repro3/repro3	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3697913	M	MP:0009230	abnormal sperm head morphology	repro3/repro3	involves: C3HeB/FeJ * C57BL/6J	N	16920728
MGI:3698024	F	MP:0001134	absent corpus luteum	Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	17046690
MGI:3698024	F	MP:0009097	absent endometrial glands	Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	17046690
MGI:3698024	F	MP:0001123	dilated uterus	Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	17046690
MGI:3698024	F	MP:0009365	abnormal theca cell layer morphology	Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	17046690
MGI:3698024	F	MP:0011128	increased tertiary ovarian follicle number	Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	17046690
MGI:3698024	F	MP:0001126	abnormal ovary morphology	Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	17046690
MGI:3698024	F	MP:0004896	abnormal endometrium morphology	Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	17046690
MGI:3698024	F	MP:0009359	endometrium atrophy	Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	17046690
MGI:3698024	F	MP:0001926	female infertility	Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	17046690
MGI:3698151	F	MP:0000715	decreased thymocyte number	Il2rg<tm1Krf>/Il2rg<tm1Krf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N)	N	10523604
MGI:3698152	F	MP:0000715	decreased thymocyte number	Il2rg<tm1Krf>/Il2rg<tm1Krf>,Tg(Igh-Pim1)1Brn/0	either: (involves: 129P2/OlaHsd * C57BL/6 * CBA) or (involves: 129P2/OlaHsd * C57BL/6 * CBA * FVB/N)	N	10523604
MGI:3698154	F	MP:0000715	decreased thymocyte number	Il2rg<tm1Krf>/Il2rg<tm1Krf>,Tg(BCL2/IGH)1Tjd/0	either: (involves: 129P2/OlaHsd * C3H/He * C57BL/6) or (involves: 129P2/OlaHsd * C3H/He * C57BL/6 * FVB/N)	N	10523604
MGI:3698299	M	MP:0002685	abnormal spermatogonia proliferation	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698299	M	MP:0001925	male infertility	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698299	M	MP:0001156	abnormal spermatogenesis	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698299	F	MP:0002777	absent ovarian follicles	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698299	M	MP:0004901	decreased male germ cell number	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698299	M	MP:0001147	small testis	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698299	F	MP:0001130	abnormal ovarian folliculogenesis	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698299	F	MP:0002682	decreased mature ovarian follicle number	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698299	F	MP:0001131	abnormal ovarian follicle morphology	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698299	M	MP:0002687	oligozoospermia	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698299	F	MP:0001750	increased circulating follicle stimulating hormone level	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698299	F	MP:0001132	absent mature ovarian follicles	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698299	F	MP:0001127	small ovary	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698299	F	MP:0001926	female infertility	Zglp1<tm1Eem>/Zglp1<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ	N	16982049
MGI:3698523	F	MP:0000063	decreased bone mineral density	Bmd37<CASA/Rk>/Bmd37<CASA/Rk>	involves: C57BL/6J * CASA/Rk	N	17179051
MGI:3698532	M	MP:0001544	abnormal cardiovascular system physiology	Fhl1<tm1Chen>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	19033658
MGI:3698532	M	MP:0005386	behavior/neurological phenotype	Fhl1<tm1Chen>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	Y	17150988
MGI:3698532	M	MP:0004486	decreased response of heart to induced stress	Fhl1<tm1Chen>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	19033658
MGI:3698532	M	MP:0005378	growth/size/body region phenotype	Fhl1<tm1Chen>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	Y	17150988
MGI:3698532	M	MP:0003631	nervous system phenotype	Fhl1<tm1Chen>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	Y	17150988
MGI:3698557	M	MP:0000428	abnormal craniofacial morphology	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	N	16964440
MGI:3698557	M	MP:0006279	abnormal limb development	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	N	16964440
MGI:3698557	M	MP:0000550	abnormal forelimb morphology	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	N	16964440
MGI:3698557	M	MP:0010768	mortality/aging	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	Y	16964440
MGI:3698557	M	MP:0002135	abnormal kidney morphology	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	N	16964440
MGI:3698557	M	MP:0000572	abnormal autopod morphology	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	N	16964440
MGI:3698557	M	MP:0002051	increased skin papilloma incidence	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	N	16964440
MGI:3698557	M	MP:0001297	microphthalmia	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	N	16964440
MGI:3698557	M	MP:0002160	abnormal reproductive system morphology	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	N	16964440
MGI:3698557	M	MP:0005389	reproductive system phenotype	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	Y	16964440
MGI:3698557	M	MP:0002113	abnormal skeleton development	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	N	16964440
MGI:3698557	M	MP:0002110	abnormal digit morphology	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	N	16964440
MGI:3698557	M	MP:0000585	kinked tail	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	N	16964440
MGI:3698557	M	MP:0003051	curly tail	Etn3<Ppd>/Y	either: (involves: CD-1) or (involves: C3H/HeJ * CD-1)	N	16964440
MGI:3698627	F	MP:0009098	anovaginal fistula	Sall4<tm1Brd>/Sall4<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	17216607
MGI:3698629	M	MP:0031286	unilateral cryptorchism	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	M	MP:0001155	arrest of spermatogenesis	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	F	MP:0009396	small endometrial glands	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	M	MP:0002286	cryptorchism	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	M	MP:0001154	seminiferous tubule degeneration	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	F	MP:0001926	female infertility	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	M	MP:0001922	reduced male fertility	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	F	MP:0001132	absent mature ovarian follicles	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	M	MP:0001147	small testis	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	F	MP:0001119	abnormal female reproductive system morphology	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	F	MP:0001376	abnormal mating receptivity	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	M	MP:0001145	abnormal male reproductive system morphology	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	F	MP:0001126	abnormal ovary morphology	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	F	MP:0001134	absent corpus luteum	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	F	MP:0002637	small uterus	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698629	M	MP:0031287	bilateral cryptorchism	Arid5b<tm1Pjh>/Arid5b<tm1Pjh>	involves: 129S4/SvJae * BALB/c	N	11483573
MGI:3698637	F	MP:0000161	scoliosis	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0000120	malocclusion	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0001706	abnormal left-right axis patterning	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0002083	premature death	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0004871	premaxilla hypoplasia	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0002258	abnormal cricoid cartilage morphology	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0003345	decreased rib number	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0030285	mandibular coronoid process hypoplasia	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0000458	abnormal mandible morphology	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0001732	postnatal growth retardation	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0000024	lowered ear position	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0031345	developmental cataract	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0000457	maxilla hypoplasia	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0000644	dextrocardia	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0005270	abnormal zygomatic bone morphology	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0000160	kyphosis	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0030100	hemifacial hypoplasia	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0009916	absent hyoid bone greater horns	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0000585	kinked tail	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0000454	abnormal jaw morphology	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0000023	abnormal ear position	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698637	F	MP:0003056	abnormal hyoid bone morphology	Zic3<tm1Jwb>/Zic3<tm1Jwb>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0030285	mandibular coronoid process hypoplasia	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0000458	abnormal mandible morphology	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0005270	abnormal zygomatic bone morphology	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0000161	scoliosis	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0003056	abnormal hyoid bone morphology	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0000120	malocclusion	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0002258	abnormal cricoid cartilage morphology	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0002083	premature death	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0001706	abnormal left-right axis patterning	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0000454	abnormal jaw morphology	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0031345	developmental cataract	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0000585	kinked tail	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0009916	absent hyoid bone greater horns	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0000160	kyphosis	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0030100	hemifacial hypoplasia	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0000024	lowered ear position	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0003345	decreased rib number	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0000644	dextrocardia	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0004871	premaxilla hypoplasia	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0011660	ectopia cordis	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0000023	abnormal ear position	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0001732	postnatal growth retardation	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698642	M	MP:0000457	maxilla hypoplasia	Zic3<tm1Jwb>/Y	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	N	17127413
MGI:3698745	F	MP:0004813	absent linear vestibular evoked potential	Pou3f4<del-J>/Pou3f4<+>	C3HeB/FeJ-Pou3f4<del-J>/J	N	16235133
MGI:3698827	F	MP:0001926	female infertility	Thra<tm1Ven>/Thra<tm1Ven>,Thrb<tm1Df>/Thrb<tm1Df>	B6.129-Thra<tm1Ven> Thrb<tm1Df>	N	11739587
MGI:3698827	M	MP:0002674	abnormal sperm motility	Thra<tm1Ven>/Thra<tm1Ven>,Thrb<tm1Df>/Thrb<tm1Df>	B6.129-Thra<tm1Ven> Thrb<tm1Df>	N	17210747
MGI:3698827	M	MP:0004852	decreased testis weight	Thra<tm1Ven>/Thra<tm1Ven>,Thrb<tm1Df>/Thrb<tm1Df>	B6.129-Thra<tm1Ven> Thrb<tm1Df>	N	17210747
MGI:3698837	F	MP:0001926	female infertility	Thra<tm1Ven>/Thra<tm1Ven>,Thrb<tm1Df>/Thrb<tm1Df>	involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6J	N	11739587
MGI:3698852	M	MP:0009325	necrospermia	Qki<qk-v>/Qki<qk-v>	B6C3Fe a/a-Qki<qk-v>/J	N	14757819
MGI:3698852	M	MP:0009230	abnormal sperm head morphology	Qki<qk-v>/Qki<qk-v>	B6C3Fe a/a-Qki<qk-v>/J	N	14757819
MGI:3698852	M	MP:0001932	abnormal spermiogenesis	Qki<qk-v>/Qki<qk-v>	B6C3Fe a/a-Qki<qk-v>/J	N	14757819
MGI:3698852	M	MP:0002687	oligozoospermia	Qki<qk-v>/Qki<qk-v>	B6C3Fe a/a-Qki<qk-v>/J	N	14757819
MGI:3698852	M	MP:0008892	abnormal sperm flagellum morphology	Qki<qk-v>/Qki<qk-v>	B6C3Fe a/a-Qki<qk-v>/J	N	14757819
MGI:3698852	M	MP:0001156	abnormal spermatogenesis	Qki<qk-v>/Qki<qk-v>	B6C3Fe a/a-Qki<qk-v>/J	N	14757819
MGI:3699143	F	MP:0001194	dermatitis	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699143	F	MP:0005092	decreased double-positive T cell number	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17353370
MGI:3699143	F	MP:0003865	lymph node inflammation	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699143	F	MP:0001823	thymus hypoplasia	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17353370
MGI:3699143	F	MP:0005350	increased susceptibility to autoimmune disorder	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699143	F	MP:0002145	abnormal T cell differentiation	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17353370
MGI:3699143	F	MP:0000691	enlarged spleen	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699143	F	MP:0001192	scaly skin	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699143	F	MP:0001860	liver inflammation	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699143	F	MP:0001861	lung inflammation	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0008126	increased dendritic cell number	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0001194	dermatitis	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0003865	lymph node inflammation	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0009763	increased susceptibility to induced morbidity/mortality	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0000691	enlarged spleen	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0005156	bradykinesia	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0005018	decreased T cell number	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0005150	cachexia	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0001861	lung inflammation	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0001860	liver inflammation	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0002376	abnormal dendritic cell physiology	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0001852	conjunctivitis	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0001263	weight loss	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699144	F	MP:0005350	increased susceptibility to autoimmune disorder	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<tm3(HBEGF/GFP)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699150	M	MP:0005350	increased susceptibility to autoimmune disorder	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699150	M	MP:0003865	lymph node inflammation	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699150	M	MP:0001861	lung inflammation	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699150	M	MP:0001192	scaly skin	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699150	M	MP:0001860	liver inflammation	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699150	M	MP:0000691	enlarged spleen	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699150	M	MP:0001194	dermatitis	Foxp3<tm1.1Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17136045
MGI:3699209	M	MP:0001147	small testis	Dmrtc2<tm1(cre)Knis>/Dmrtc2<tm1(cre)Knis>	involves: 129P2/OlaHsd * C57BL/6J	N	17098235
MGI:3699209	M	MP:0001940	testis hypoplasia	Dmrtc2<tm1(cre)Knis>/Dmrtc2<tm1(cre)Knis>	involves: 129P2/OlaHsd * C57BL/6J	N	17098235
MGI:3699209	M	MP:0006380	abnormal spermatid morphology	Dmrtc2<tm1(cre)Knis>/Dmrtc2<tm1(cre)Knis>	involves: 129P2/OlaHsd * C57BL/6J	N	17098235
MGI:3699209	M	MP:0005159	azoospermia	Dmrtc2<tm1(cre)Knis>/Dmrtc2<tm1(cre)Knis>	involves: 129P2/OlaHsd * C57BL/6J	N	17098235
MGI:3699209	M	MP:0008261	arrest of male meiosis	Dmrtc2<tm1(cre)Knis>/Dmrtc2<tm1(cre)Knis>	involves: 129P2/OlaHsd * C57BL/6J	N	17098235
MGI:3699214	F	MP:0003787	abnormal imprinting	Tsix<tm3Jtl>/Tsix<+>	involves: 129	N	17199041
MGI:3699214	F	MP:0001935	decreased litter size	Tsix<tm3Jtl>/Tsix<+>	involves: 129	N	17199041
MGI:3699214	F	MP:0011103	embryonic lethality at implantation, incomplete penetrance	Tsix<tm3Jtl>/Tsix<+>	involves: 129	N	17199041
MGI:3699214	F	MP:0008770	decreased survivor rate	Tsix<tm3Jtl>/Tsix<+>	involves: 129	N	17199041
MGI:3699216	M	MP:0011103	embryonic lethality at implantation, incomplete penetrance	Tsix<tm3Jtl>/Y	involves: 129	N	17199041
MGI:3699216	M	MP:0003787	abnormal imprinting	Tsix<tm3Jtl>/Y	involves: 129	N	17199041
MGI:3699216	M	MP:0008770	decreased survivor rate	Tsix<tm3Jtl>/Y	involves: 129	N	17199041
MGI:3699217	F	MP:0011091	prenatal lethality, complete penetrance	Tsix<tm3Jtl>/Tsix<tm3Jtl>	involves: 129	N	17199041
MGI:3699221	M	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Tsix<tm2Jtl>/Y	involves: 129 * M. m. castaneus	N	10520993
MGI:3699221	M	MP:0003787	abnormal imprinting	Tsix<tm2Jtl>/Y	involves: 129 * M. m. castaneus	N	10520993
MGI:3699222	F	MP:0002080	prenatal lethality	Tsix<tm2Jtl>/Tsix<+>	involves: 129 * M. m. castaneus	N	10520993
MGI:3699222	F	MP:0003787	abnormal imprinting	Tsix<tm2Jtl>/Tsix<+>	involves: 129 * M. m. castaneus	N	10520993
MGI:3699222	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Tsix<tm2Jtl>/Tsix<+>	involves: 129 * M. m. castaneus	N	10520993
MGI:3699285	M	MP:0001922	reduced male fertility	Sulf2<Gt(XST155)Byg>/Sulf2<Gt(XST155)Byg>	FVB.129P2(B6)-Sulf2<Gt(XST155)Byg>	N	17116694
MGI:3699285	F	MP:0001923	reduced female fertility	Sulf2<Gt(XST155)Byg>/Sulf2<Gt(XST155)Byg>	FVB.129P2(B6)-Sulf2<Gt(XST155)Byg>	N	17116694
MGI:3699324	M	MP:0001922	reduced male fertility	Grid2<ho-Jwg>/Grid2<ho-Jwg>	Not Specified	N	1689261
MGI:3699324	M	MP:0002674	abnormal sperm motility	Grid2<ho-Jwg>/Grid2<ho-Jwg>	Not Specified	N	1689261
MGI:3699324	M	MP:0008892	abnormal sperm flagellum morphology	Grid2<ho-Jwg>/Grid2<ho-Jwg>	Not Specified	N	1689261
MGI:3699324	M	MP:0001922	reduced male fertility	Grid2<ho-Jwg>/Grid2<ho-Jwg>	Not Specified	N	MGI:62315
MGI:3699324	M	MP:0000242	impaired fertilization	Grid2<ho-Jwg>/Grid2<ho-Jwg>	Not Specified	N	1689261
MGI:3699324	F	MP:0001923	reduced female fertility	Grid2<ho-Jwg>/Grid2<ho-Jwg>	Not Specified	N	1689261
MGI:3699324	M	MP:0030976	impaired sperm penetration of zona pellucida	Grid2<ho-Jwg>/Grid2<ho-Jwg>	Not Specified	N	1689261
MGI:3699501	M	MP:0011087	neonatal lethality, complete penetrance	Cask<tm1.1Sud>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	17287346
MGI:3699502	F	MP:0005445	abnormal neurotransmitter secretion	Cask<tm1Sud>/Cask<tm1.1Sud>,Tg(Prm-cre)58Og/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	17287346
MGI:3699502	F	MP:0003631	nervous system phenotype	Cask<tm1Sud>/Cask<tm1.1Sud>,Tg(Prm-cre)58Og/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	Y	17287346
MGI:3699502	F	MP:0009890	cleft secondary palate	Cask<tm1Sud>/Cask<tm1.1Sud>,Tg(Prm-cre)58Og/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	17287346
MGI:3699502	F	MP:0009888	palatal shelves fail to meet at midline	Cask<tm1Sud>/Cask<tm1.1Sud>,Tg(Prm-cre)58Og/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	17287346
MGI:3699502	F	MP:0001953	respiratory failure	Cask<tm1Sud>/Cask<tm1.1Sud>,Tg(Prm-cre)58Og/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	17287346
MGI:3699502	F	MP:0003203	increased neuron apoptosis	Cask<tm1Sud>/Cask<tm1.1Sud>,Tg(Prm-cre)58Og/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	17287346
MGI:3699502	F	MP:0011087	neonatal lethality, complete penetrance	Cask<tm1Sud>/Cask<tm1.1Sud>,Tg(Prm-cre)58Og/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	17287346
MGI:3699503	F	MP:0001265	decreased body size	Cask<tm1Sud>/Cask<tm1Sud>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	17287346
MGI:3699815	F	MP:0001262	decreased body weight	Aifm1<Hq>/Aifm1<Hq>	involves: CF-1	N	MGI:63213
MGI:3699815	F	MP:0000418	focal hair loss	Aifm1<Hq>/Aifm1<Hq>	involves: CF-1	N	MGI:63213
MGI:3699816	M	MP:0000418	focal hair loss	Aifm1<Hq>/Y	involves: CF-1	N	MGI:63213
MGI:3699816	M	MP:0001262	decreased body weight	Aifm1<Hq>/Y	involves: CF-1	N	MGI:63213
MGI:3699821	F	MP:0003204	decreased neuron apoptosis	Aifm1<Hq>/Aifm1<Hq>,Apaf1<Gt(IRESBetageo)XIX18Pgr>/Apaf1<Gt(IRESBetageo)XIX18Pgr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	15703386
MGI:3699888	F	MP:0003131	increased erythrocyte cell number	Bmrbc4<C57BL/6Ola>/Bmrbc4<C57BL/6Ola>	involves: C57BL/6Ola * CBA/HOla	N	17185011
MGI:3699889	F	MP:0003131	increased erythrocyte cell number	Bmrbc4<C57BL/6Ola>/Bmrbc4<CBA/HOla>	involves: C57BL/6Ola * CBA/HOla	N	17185011
MGI:3699890	F	MP:0003131	increased erythrocyte cell number	Bmrbc4<CBA/HOla>/Bmrbc4<CBA/HOla>	involves: C57BL/6Ola * CBA/HOla	N	17185011
MGI:3699951	M	MP:0010402	ventricular septal defect	Flna<tm1.2Caw>/Y	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699951	M	MP:0000260	abnormal angiogenesis	Flna<tm1.2Caw>/Y	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699951	M	MP:0004157	interrupted aortic arch	Flna<tm1.2Caw>/Y	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699951	M	MP:0010403	atrial septal defect	Flna<tm1.2Caw>/Y	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699951	M	MP:0001914	hemorrhage	Flna<tm1.2Caw>/Y	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699951	M	MP:0006126	abnormal cardiac outflow tract development	Flna<tm1.2Caw>/Y	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699951	M	MP:0000364	abnormal vascular regression	Flna<tm1.2Caw>/Y	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699951	M	MP:0002633	persistent truncus arteriosus	Flna<tm1.2Caw>/Y	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699951	M	MP:0001785	edema	Flna<tm1.2Caw>/Y	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699951	M	MP:0010432	common ventricle	Flna<tm1.2Caw>/Y	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699951	M	MP:0012253	abnormal intersomitic vessel morphology	Flna<tm1.2Caw>/Y	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699951	M	MP:0001614	abnormal blood vessel morphology	Flna<tm1.2Caw>/Y	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699951	M	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance	Flna<tm1.2Caw>/Y	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699952	F	MP:0001923	reduced female fertility	Flna<tm1.2Caw>/Flna<+>	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699952	F	MP:0001785	edema	Flna<tm1.2Caw>/Flna<+>	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699952	F	MP:0000266	abnormal heart morphology	Flna<tm1.2Caw>/Flna<+>	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699952	F	MP:0004937	dilated heart	Flna<tm1.2Caw>/Flna<+>	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699952	F	MP:0001654	hepatic necrosis	Flna<tm1.2Caw>/Flna<+>	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699952	F	MP:0011110	preweaning lethality, incomplete penetrance	Flna<tm1.2Caw>/Flna<+>	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699952	F	MP:0001958	emphysema	Flna<tm1.2Caw>/Flna<+>	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699952	F	MP:0011086	postnatal lethality, incomplete penetrance	Flna<tm1.2Caw>/Flna<+>	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699952	F	MP:0005048	abnormal thrombosis	Flna<tm1.2Caw>/Flna<+>	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699952	F	MP:0000218	increased leukocyte cell number	Flna<tm1.2Caw>/Flna<+>	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699952	F	MP:0002083	premature death	Flna<tm1.2Caw>/Flna<+>	involves: 129S4/SvJae * C57BL/6	N	17172441
MGI:3699953	M	MP:0001575	cyanosis	Flna<tm1.1Caw>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJae * C57BL/6 * CBA	N	17172441
MGI:3699953	M	MP:0000771	abnormal brain size	Flna<tm1.1Caw>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJae * C57BL/6 * CBA	N	17172441
MGI:3699953	M	MP:0001614	abnormal blood vessel morphology	Flna<tm1.1Caw>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJae * C57BL/6 * CBA	N	17172441
MGI:3699953	M	MP:0004003	abnormal vascular endothelial cell physiology	Flna<tm1.1Caw>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJae * C57BL/6 * CBA	N	17172441
MGI:3699953	M	MP:0002633	persistent truncus arteriosus	Flna<tm1.1Caw>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJae * C57BL/6 * CBA	N	17172441
MGI:3699953	M	MP:0006126	abnormal cardiac outflow tract development	Flna<tm1.1Caw>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJae * C57BL/6 * CBA	N	17172441
MGI:3699953	M	MP:0011087	neonatal lethality, complete penetrance	Flna<tm1.1Caw>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJae * C57BL/6 * CBA	N	17172441
MGI:3699953	M	MP:0000297	abnormal atrioventricular cushion morphology	Flna<tm1.1Caw>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJae * C57BL/6 * CBA	N	17172441
MGI:3699953	M	MP:0005386	behavior/neurological phenotype	Flna<tm1.1Caw>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJae * C57BL/6 * CBA	Y	17172441
MGI:3699953	M	MP:0006055	abnormal vascular endothelial cell morphology	Flna<tm1.1Caw>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJae * C57BL/6 * CBA	N	17172441
MGI:3699953	M	MP:0004157	interrupted aortic arch	Flna<tm1.1Caw>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJae * C57BL/6 * CBA	N	17172441
MGI:3700038	M	MP:0001155	arrest of spermatogenesis	Lmtk2<tm1Tya>/Lmtk2<tm1Tya>	involves: 129P2/OlaHsd * C57BL/6	N	17158803
MGI:3700038	M	MP:0005159	azoospermia	Lmtk2<tm1Tya>/Lmtk2<tm1Tya>	involves: 129P2/OlaHsd * C57BL/6	N	17158803
MGI:3700038	M	MP:0001925	male infertility	Lmtk2<tm1Tya>/Lmtk2<tm1Tya>	involves: 129P2/OlaHsd * C57BL/6	N	17158803
MGI:3700038	M	MP:0001147	small testis	Lmtk2<tm1Tya>/Lmtk2<tm1Tya>	involves: 129P2/OlaHsd * C57BL/6	N	17158803
MGI:3700128	M	MP:0001154	seminiferous tubule degeneration	Alms1<L2131X>/Alms1<L2131X>	involves: C57BL/6 * NOD	N	17206865
MGI:3700128	M	MP:0001156	abnormal spermatogenesis	Alms1<L2131X>/Alms1<L2131X>	involves: C57BL/6 * NOD	N	17206865
MGI:3700129	M	MP:0001925	male infertility	Stk36<tm1Fjs>/Stk36<tm1Fjs>	involves: 129S1/Sv * C57BL/6	N	16055717
MGI:3700171	M	MP:0004851	increased testis weight	Plcb1<Tg(LGB)56Mbal>/Plcb1<Tg(LGB)56Mbal>	involves: C57BL/6 * CBA	N	15474310
MGI:3700171	F	MP:0001923	reduced female fertility	Plcb1<Tg(LGB)56Mbal>/Plcb1<Tg(LGB)56Mbal>	involves: C57BL/6 * CBA	N	15474310
MGI:3700171	M	MP:0001922	reduced male fertility	Plcb1<Tg(LGB)56Mbal>/Plcb1<Tg(LGB)56Mbal>	involves: C57BL/6 * CBA	N	15474310
MGI:3700246	M	MP:0001922	reduced male fertility	Celf1<tm1Cba>/Celf1<tm1Cba>	involves: 129S2/SvPas * C57BL/6	N	17130239
MGI:3700246	M	MP:0001925	male infertility	Celf1<tm1Cba>/Celf1<tm1Cba>	involves: 129S2/SvPas * C57BL/6	N	17130239
MGI:3700246	F	MP:0001923	reduced female fertility	Celf1<tm1Cba>/Celf1<tm1Cba>	involves: 129S2/SvPas * C57BL/6	N	17130239
MGI:3700246	M	MP:0001155	arrest of spermatogenesis	Celf1<tm1Cba>/Celf1<tm1Cba>	involves: 129S2/SvPas * C57BL/6	N	17130239
MGI:3700375	F	MP:0000598	abnormal liver morphology	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700375	F	MP:0000351	increased cell proliferation	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700375	F	MP:0001845	abnormal inflammatory response	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700375	F	MP:0005560	decreased circulating glucose level	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700375	F	MP:0002941	increased circulating alanine transaminase level	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700375	F	MP:0002628	hepatic steatosis	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700375	F	MP:0001860	liver inflammation	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700375	F	MP:0005584	abnormal enzyme/coenzyme activity	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700375	F	MP:0003331	increased hepatocellular carcinoma incidence	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700375	F	MP:0000607	abnormal hepatocyte morphology	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700375	F	MP:0006042	increased apoptosis	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700375	F	MP:0008735	increased susceptibility to endotoxin shock	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	18606991
MGI:3700375	F	MP:0014341	abnormal hepatocyte mitochondrial morphology	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700375	F	MP:0003009	abnormal cytokine secretion	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700376	F	MP:0002942	decreased circulating alanine transaminase level	Fadd<tm1Mpa>/Fadd<tm1Mpa>,Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700376	F	MP:0006043	decreased apoptosis	Fadd<tm1Mpa>/Fadd<tm1Mpa>,Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700376	F	MP:0005370	liver/biliary system phenotype	Fadd<tm1Mpa>/Fadd<tm1Mpa>,Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	Y	17292824
MGI:3700376	F	MP:0001860	liver inflammation	Fadd<tm1Mpa>/Fadd<tm1Mpa>,Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700376	F	MP:0005584	abnormal enzyme/coenzyme activity	Fadd<tm1Mpa>/Fadd<tm1Mpa>,Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N	N	17292824
MGI:3700541	F	MP:0002169	no abnormal phenotype detected	Foxp3<tm2Flv>/Foxp3<+>	involves: C57BL/6	N	17220876
MGI:3700542	M	MP:0005251	blepharitis	Foxp3<tm2Flv>/Y	involves: C57BL/6	N	17220876
MGI:3700542	M	MP:0002083	premature death	Foxp3<tm2Flv>/Y	involves: C57BL/6	N	17220876
MGI:3700542	M	MP:0003725	increased autoantibody level	Foxp3<tm2Flv>/Y	involves: C57BL/6	N	17220876
MGI:3700542	M	MP:0001790	abnormal immune system physiology	Foxp3<tm2Flv>/Y	involves: C57BL/6	N	17220876
MGI:3700542	M	MP:0000702	enlarged lymph nodes	Foxp3<tm2Flv>/Y	involves: C57BL/6	N	17220876
MGI:3700542	M	MP:0000691	enlarged spleen	Foxp3<tm2Flv>/Y	involves: C57BL/6	N	17220876
MGI:3700542	M	MP:0001265	decreased body size	Foxp3<tm2Flv>/Y	involves: C57BL/6	N	17220876
MGI:3700542	M	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology	Foxp3<tm2Flv>/Y	involves: C57BL/6	N	17220876
MGI:3700542	M	MP:0001925	male infertility	Foxp3<tm2Flv>/Y	involves: C57BL/6	N	17220876
MGI:3700542	M	MP:0001192	scaly skin	Foxp3<tm2Flv>/Y	involves: C57BL/6	N	17220876
MGI:3700542	M	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology	Foxp3<tm2Flv>/Y	involves: C57BL/6	N	17220876
MGI:3700545	M	MP:0001147	small testis	Nr0b2<tm1.1Auw>/Nr0b2<tm1.1Auw>	involves: 129S2/SvPas * C57BL/6J	N	17289919
MGI:3700545	M	MP:0004884	abnormal testis physiology	Nr0b2<tm1.1Auw>/Nr0b2<tm1.1Auw>	involves: 129S2/SvPas * C57BL/6J	N	17289919
MGI:3700545	M	MP:0004852	decreased testis weight	Nr0b2<tm1.1Auw>/Nr0b2<tm1.1Auw>	involves: 129S2/SvPas * C57BL/6J	N	17289919
MGI:3700545	M	MP:0004928	increased epididymis weight	Nr0b2<tm1.1Auw>/Nr0b2<tm1.1Auw>	involves: 129S2/SvPas * C57BL/6J	N	17289919
MGI:3700547	M	MP:0004910	decreased seminal vesicle weight	Nr5a2<tm1Auw>/Nr5a2<+>	involves: C57BL/6J	N	17289919
MGI:3700547	M	MP:0004929	decreased epididymis weight	Nr5a2<tm1Auw>/Nr5a2<+>	involves: C57BL/6J	N	17289919
MGI:3700686	M	MP:0001925	male infertility	Cacng2<stg>/Cacng2<stg>	B6C3Fe a/a-Cacng2<stg>	N	2289471
MGI:3700822	M	MP:0001147	small testis	Terc<tm1Rdp>/Terc<tm1Rdp>,Wrn<tm1Lgu>/Wrn<tm1Lgu>	involves: 129/Sv * BALB/c * C57BL/6 * SLJ	N	15235603
MGI:3700836	M	MP:0031605	decreased susceptibility to age-related retinal degeneration	Arrd4<C57BL/6J>/Y	involves: A/J * C57BL/6J	N	17277741
MGI:3700984	F	MP:0001923	reduced female fertility	Tbx6<rv>/Tbx6<rv>	involves: C57BL/J * C57BL/6J	N	4073528
MGI:3701228	F	MP:0009433	polyovular ovarian follicle	Dmrta1<tm1.1Zark>/Dmrta1<tm1.1Zark>	involves: 129S1/Sv * FVB/N	N	16982677
MGI:3701228	M	MP:0001375	abnormal mating preference	Dmrta1<tm1.1Zark>/Dmrta1<tm1.1Zark>	involves: 129S1/Sv * FVB/N	N	16982677
MGI:3701228	M	MP:0031629	abnormal mounting behavior	Dmrta1<tm1.1Zark>/Dmrta1<tm1.1Zark>	involves: 129S1/Sv * FVB/N	N	16982677
MGI:3701229	M	MP:0031629	abnormal mounting behavior	Dmrta1<tm1.1Zark>/Dmrta1<+>	involves: 129S1/Sv * FVB/N	N	16982677
MGI:3701229	F	MP:0009433	polyovular ovarian follicle	Dmrta1<tm1.1Zark>/Dmrta1<+>	involves: 129S1/Sv * FVB/N	N	16982677
MGI:3701498	F	MP:0008000	increased ovary tumor incidence	Smad4<m4Mag>/Smad4<+>	involves: 129S/Sv * Black Swiss * C57BL/6	N	16518688
MGI:3701530	F	MP:0009506	abnormal mammary gland alveolus morphology	Mrtfa<tm1Swm>/Mrtfa<tm1Swm>	involves: 129/Sv * C57BL/6	N	16847333
MGI:3701530	F	MP:0001882	abnormal lactation	Mrtfa<tm1Swm>/Mrtfa<tm1Swm>	involves: 129/Sv * C57BL/6	N	16847333
MGI:3701530	F	MP:0001881	abnormal mammary gland physiology	Mrtfa<tm1Swm>/Mrtfa<tm1Swm>	involves: 129/Sv * C57BL/6	N	16847333
MGI:3701530	F	MP:0014126	increased mammary gland apoptosis	Mrtfa<tm1Swm>/Mrtfa<tm1Swm>	involves: 129/Sv * C57BL/6	N	16847333
MGI:3701530	F	MP:0000627	abnormal mammary gland morphology	Mrtfa<tm1Swm>/Mrtfa<tm1Swm>	involves: 129/Sv * C57BL/6	N	16847333
MGI:3701530	F	MP:0013779	abnormal mammary gland myoepithelium physiology	Mrtfa<tm1Swm>/Mrtfa<tm1Swm>	involves: 129/Sv * C57BL/6	N	16847333
MGI:3701530	F	MP:0009504	abnormal mammary gland epithelium morphology	Mrtfa<tm1Swm>/Mrtfa<tm1Swm>	involves: 129/Sv * C57BL/6	N	16847333
MGI:3701530	F	MP:0013719	pale mammary gland	Mrtfa<tm1Swm>/Mrtfa<tm1Swm>	involves: 129/Sv * C57BL/6	N	16847333
MGI:3701530	F	MP:0013718	galactostasis	Mrtfa<tm1Swm>/Mrtfa<tm1Swm>	involves: 129/Sv * C57BL/6	N	16847333
MGI:3701530	F	MP:0006271	abnormal involution of the mammary gland	Mrtfa<tm1Swm>/Mrtfa<tm1Swm>	involves: 129/Sv * C57BL/6	N	16847333
MGI:3701960	F	MP:0003845	abnormal decidualization	Mug1<tm2Vln>/Mug1<tm2Vln>,Pzp<tm1Vln>/Pzp<tm1Vln>	B.129P2-Pzp<tm1Vln> Mug1<tm2Vln>	N	14580373
MGI:3701960	F	MP:0004014	abnormal uterine environment	Mug1<tm2Vln>/Mug1<tm2Vln>,Pzp<tm1Vln>/Pzp<tm1Vln>	B.129P2-Pzp<tm1Vln> Mug1<tm2Vln>	N	14580373
MGI:3701960	F	MP:0004256	abnormal maternal decidual layer morphology	Mug1<tm2Vln>/Mug1<tm2Vln>,Pzp<tm1Vln>/Pzp<tm1Vln>	B.129P2-Pzp<tm1Vln> Mug1<tm2Vln>	N	14580373
MGI:3701960	F	MP:0008054	abnormal uterine NK cell morphology	Mug1<tm2Vln>/Mug1<tm2Vln>,Pzp<tm1Vln>/Pzp<tm1Vln>	B.129P2-Pzp<tm1Vln> Mug1<tm2Vln>	N	14580373
MGI:3702282	F	MP:0009088	thin uterine horn	Ap3b1<pe>/Ap3b1<pe>	involves: C3H/He * C57BL/6J	N	32016796
MGI:3702282	F	MP:0002637	small uterus	Ap3b1<pe>/Ap3b1<pe>	involves: C3H/He * C57BL/6J	N	32016796
MGI:3702282	F	MP:0001935	decreased litter size	Ap3b1<pe>/Ap3b1<pe>	involves: C3H/He * C57BL/6J	N	32016796
MGI:3702282	F	MP:0009089	short uterine horn	Ap3b1<pe>/Ap3b1<pe>	involves: C3H/He * C57BL/6J	N	32016796
MGI:3702282	F	MP:0001121	uterus hypoplasia	Ap3b1<pe>/Ap3b1<pe>	involves: C3H/He * C57BL/6J	N	32016796
MGI:3702282	F	MP:0008258	thin endometrium	Ap3b1<pe>/Ap3b1<pe>	involves: C3H/He * C57BL/6J	N	32016796
MGI:3702677	M	MP:0001925	male infertility	olt/olt	involves: C3H/HeJOrl	N	MGI:72494
MGI:3702677	M	MP:0001156	abnormal spermatogenesis	olt/olt	involves: C3H/HeJOrl	N	1399832
MGI:3702677	M	MP:0008279	arrest of spermiogenesis	olt/olt	involves: C3H/HeJOrl	N	MGI:78429
MGI:3702677	M	MP:0008279	arrest of spermiogenesis	olt/olt	involves: C3H/HeJOrl	N	8025157
MGI:3702677	M	MP:0005159	azoospermia	olt/olt	involves: C3H/HeJOrl	N	MGI:72494
MGI:3702677	M	MP:0004852	decreased testis weight	olt/olt	involves: C3H/HeJOrl	N	1399832
MGI:3702677	M	MP:0006380	abnormal spermatid morphology	olt/olt	involves: C3H/HeJOrl	N	1399832
MGI:3702696	M	MP:0005159	azoospermia	Nanos2<tm1Ysa>/Nanos2<tm1Ysa>	involves: 129S1/Sv * 129X1/SvJ	N	18281459
MGI:3702696	M	MP:0006362	abnormal male germ cell morphology	Nanos2<tm1Ysa>/Nanos2<tm1Ysa>	involves: 129S1/Sv * 129X1/SvJ	N	18281459
MGI:3702700	F	MP:0030982	abnormal copulatory plug deposition	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0001938	delayed sexual maturation	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0001134	absent corpus luteum	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0009945	abnormal accessory olfactory bulb morphology	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0001262	decreased body weight	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0001728	failure of embryo implantation	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0009674	decreased birth weight	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0008544	impaired olfaction	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0030983	failure of copulatory plug deposition	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0008948	decreased neuron number	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0001926	female infertility	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0001750	increased circulating follicle stimulating hormone level	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0001923	reduced female fertility	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0003355	decreased ovulation rate	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0031420	decreased superovulation rate	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0002566	abnormal sexual interaction	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0009649	delayed embryo implantation	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0000662	abnormal branching of the mammary ductal tree	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	M	MP:0006058	decreased cerebral infarct size	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	17301160
MGI:3702700	F	MP:0002636	delayed vaginal opening	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702700	F	MP:0001927	abnormal estrous cycle	Olfm1<tm1.1Lex>/Olfm1<tm1.1Lex>	involves: 129S/SvEvBrd * 129S4/SvJae	N	26107991
MGI:3702914	F	MP:0008000	increased ovary tumor incidence	Atm<tm1Mfl>/Atm<+>	involves: 129T2/SvEms * C57BL/6J	N	12195425
MGI:3703151	M	MP:0004901	decreased male germ cell number	Dmrt1<tm1.1Zark>/Dmrt1<tm1.1Zark>	involves: 129 * C57BL/6	N	11040213
MGI:3703151	M	MP:0002216	abnormal seminiferous tubule morphology	Dmrt1<tm1.1Zark>/Dmrt1<tm1.1Zark>	involves: 129 * C57BL/6	N	11040213
MGI:3703151	M	MP:0031407	increased Sertoli cell proliferation	Dmrt1<tm1.1Zark>/Dmrt1<tm1.1Zark>	involves: 129 * C57BL/6	N	11040213
MGI:3703151	M	MP:0002784	abnormal Sertoli cell morphology	Dmrt1<tm1.1Zark>/Dmrt1<tm1.1Zark>	involves: 129 * C57BL/6	N	11040213
MGI:3703151	M	MP:0001147	small testis	Dmrt1<tm1.1Zark>/Dmrt1<tm1.1Zark>	involves: 129 * C57BL/6	N	11040213
MGI:3703151	M	MP:0001925	male infertility	Dmrt1<tm1.1Zark>/Dmrt1<tm1.1Zark>	involves: 129 * C57BL/6	N	11040213
MGI:3703151	M	MP:0005169	abnormal male meiosis	Dmrt1<tm1.1Zark>/Dmrt1<tm1.1Zark>	involves: 129 * C57BL/6	N	11040213
MGI:3703151	M	MP:0003830	abnormal testis development	Dmrt1<tm1.1Zark>/Dmrt1<tm1.1Zark>	involves: 129 * C57BL/6	N	11040213
MGI:3703450	M	MP:0004852	decreased testis weight	Ts(17<16>)65Dn/0	involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	N	17050550
MGI:3703450	M	MP:0002784	abnormal Sertoli cell morphology	Ts(17<16>)65Dn/0	involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	N	15859352
MGI:3703450	M	MP:0006362	abnormal male germ cell morphology	Ts(17<16>)65Dn/0	involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	N	17050550
MGI:3703450	M	MP:0002687	oligozoospermia	Ts(17<16>)65Dn/0	involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	N	17050550
MGI:3703450	M	MP:0008261	arrest of male meiosis	Ts(17<16>)65Dn/0	involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	N	17050550
MGI:3703450	M	MP:0001156	abnormal spermatogenesis	Ts(17<16>)65Dn/0	involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	N	15859352
MGI:3703450	M	MP:0001156	abnormal spermatogenesis	Ts(17<16>)65Dn/0	involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	N	17050550
MGI:3703450	M	MP:0001146	abnormal testis morphology	Ts(17<16>)65Dn/0	involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	N	15859352
MGI:3703450	M	MP:0001925	male infertility	Ts(17<16>)65Dn/0	involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	N	17050550
MGI:3703450	M	MP:0020451	decreased sperm progressive motility	Ts(17<16>)65Dn/0	involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	N	17050550
MGI:3703450	M	MP:0004852	decreased testis weight	Ts(17<16>)65Dn/0	involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	N	15859352
MGI:3704019	F	MP:0001923	reduced female fertility	Por<tm2Ding>/Por<tm2Ding>	involves: 129S1/Sv * C57BL/6	N	15328377
MGI:3705023	M	MP:0013318	abnormal branching involved in seminal vesicle morphogenesis	Fgfr2<tm1.1Dor>/Fgfr2<svs>	involves: 129X1/SvJ * CXB5/ByJ * FVB/N	N	17202188
MGI:3705088	M	MP:0000666	decreased prostate gland duct number	Fgfr2<svs>/Fgfr2<svs>	involves: CXB5/ByJ	N	12666202
MGI:3705088	M	MP:0013904	abnormal seminal vesicle muscle layer morphology	Fgfr2<svs>/Fgfr2<svs>	involves: CXB5/ByJ	N	12666202
MGI:3705088	M	MP:0002059	abnormal seminal vesicle morphology	Fgfr2<svs>/Fgfr2<svs>	involves: CXB5/ByJ	N	12666202
MGI:3705088	M	MP:0004961	increased prostate gland weight	Fgfr2<svs>/Fgfr2<svs>	involves: CXB5/ByJ	N	12666202
MGI:3705088	M	MP:0013317	abnormal seminal vesicle development	Fgfr2<svs>/Fgfr2<svs>	involves: CXB5/ByJ	N	12666202
MGI:3705088	M	MP:0009736	abnormal prostate gland branching morphogenesis	Fgfr2<svs>/Fgfr2<svs>	involves: CXB5/ByJ	N	12666202
MGI:3706335	F	MP:0006270	abnormal mammary gland growth during lactation	Itgb1<tm1Mll>/Itgb1<tm1Mll>,Tg(Wap-cre)1Gsc/0	involves: 129X1/SvJ * FVB/N	N	15889143
MGI:3706335	F	MP:0000627	abnormal mammary gland morphology	Itgb1<tm1Mll>/Itgb1<tm1Mll>,Tg(Wap-cre)1Gsc/0	involves: 129X1/SvJ * FVB/N	N	15889143
MGI:3706341	F	MP:0006270	abnormal mammary gland growth during lactation	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Itgb1<tm1Mll>/Itgb1<tm1Mll>,Tg(Wap-cre)1Gsc/0	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 * FVB/N	N	15889143
MGI:3706343	F	MP:0000693	spleen hyperplasia	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	N	10655105
MGI:3706343	F	MP:0002962	increased urine protein level	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	N	10655105
MGI:3706343	M	MP:0009592	increased Leydig cell tumor incidence	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	N	11507077
MGI:3706343	F	MP:0002083	premature death	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	N	10655105
MGI:3706343	F	MP:0004762	increased anti-double stranded DNA antibody level	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	N	10655105
MGI:3706343	F	MP:0002743	glomerulonephritis	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	N	10655105
MGI:3706343	F	MP:0000691	enlarged spleen	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	N	10655105
MGI:3706343	F	MP:0004952	increased spleen weight	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	N	10655105
MGI:3706343	F	MP:0005005	abnormal self tolerance	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	N	10655105
MGI:3706516	M	MP:0001925	male infertility	Nxph1<tm1Sud>/Nxph1<tm1Sud>	involves: 129S6/SvEvTac	N	9856994
MGI:3706516	M	MP:0001156	abnormal spermatogenesis	Nxph1<tm1Sud>/Nxph1<tm1Sud>	involves: 129S6/SvEvTac	N	9856994
MGI:3706701	M	MP:0011967	increased or absent threshold for auditory brainstem response	tmgc65/tmgc65	involves: C3H/Rl * C57BL/6 * C57BL/LiA	N	16949226
MGI:3706701	M	MP:0006325	impaired hearing	tmgc65/tmgc65	involves: C3H/Rl * C57BL/6 * C57BL/LiA	N	16949226
MGI:3706806	F	MP:0002075	abnormal coat/hair pigmentation	Tg(Tyr)3412ARpw/Tg(Tyr)3412ARpw	FVB/NJ-Tg(Tyr)3412ARpw	N	MGI:3706572
MGI:3706808	M	MP:0002075	abnormal coat/hair pigmentation	Tg(Tyr)3412ARpw/Y	FVB/NJ-Tg(Tyr)3412ARpw	N	MGI:3706572
MGI:3706813	F	MP:0008000	increased ovary tumor incidence	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	N	17254969
MGI:3706813	F	MP:0002048	increased lung adenoma incidence	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	N	17254969
MGI:3706813	F	MP:0009442	increased ovarian teratoma incidence	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	N	17254969
MGI:3706813	F	MP:0012437	increased Harderian gland tumor incidence	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	N	17254969
MGI:3706813	F	MP:0002041	increased pituitary adenoma incidence	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	N	17254969
MGI:3706813	F	MP:0002020	increased tumor incidence	Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	N	17254969
MGI:3706818	F	MP:0003667	increased hemangiosarcoma incidence	Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	N	17254969
MGI:3706818	F	MP:0002947	increased hemangioma incidence	Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	N	17254969
MGI:3706818	F	MP:0002047	increased hepatic hemangioma incidence	Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	N	17254969
MGI:3706818	F	MP:0010306	increased hamartoma incidence	Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	N	17254969
MGI:3706818	F	MP:0002083	premature death	Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	N	17254969
MGI:3706822	F	MP:0003667	increased hemangiosarcoma incidence	Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	N	17254969
MGI:3706822	F	MP:0002947	increased hemangioma incidence	Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	N	17254969
MGI:3706822	F	MP:0010306	increased hamartoma incidence	Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	N	17254969
MGI:3706822	F	MP:0002024	increased T cell derived lymphoma incidence	Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	N	17254969
MGI:3706822	F	MP:0002083	premature death	Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	N	17254969
MGI:3706825	M	MP:0005578	teratozoospermia	H1f7<tm1Yoni>/H1f7<tm1Yoni>	involves: 129S1/Sv * C57BL/6	N	16055721
MGI:3706825	M	MP:0001156	abnormal spermatogenesis	H1f7<tm1Yoni>/H1f7<tm1Yoni>	involves: 129S1/Sv * C57BL/6	N	16055721
MGI:3706825	M	MP:0001925	male infertility	H1f7<tm1Yoni>/H1f7<tm1Yoni>	involves: 129S1/Sv * C57BL/6	N	16055721
MGI:3706825	M	MP:0004543	abnormal sperm physiology	H1f7<tm1Yoni>/H1f7<tm1Yoni>	involves: 129S1/Sv * C57BL/6	N	16055721
MGI:3706825	M	MP:0002675	asthenozoospermia	H1f7<tm1Yoni>/H1f7<tm1Yoni>	involves: 129S1/Sv * C57BL/6	N	16055721
MGI:3706828	F	MP:0012437	increased Harderian gland tumor incidence	Foxo3<tm1.1Rdp>/Foxo3<+>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	N	17254969
MGI:3706828	F	MP:0008000	increased ovary tumor incidence	Foxo3<tm1.1Rdp>/Foxo3<+>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	N	17254969
MGI:3706828	F	MP:0002041	increased pituitary adenoma incidence	Foxo3<tm1.1Rdp>/Foxo3<+>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	N	17254969
MGI:3706828	F	MP:0002020	increased tumor incidence	Foxo3<tm1.1Rdp>/Foxo3<+>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	N	17254969
MGI:3706951	M	MP:0004852	decreased testis weight	Ts(10<16>)232Dn/0	involves: C3H/HeSnJ * C57BL/6JEiJ	N	17050550
MGI:3706951	M	MP:0001925	male infertility	Ts(10<16>)232Dn/0	involves: C3H/HeSnJ * C57BL/6JEiJ	N	17050550
MGI:3706951	M	MP:0006362	abnormal male germ cell morphology	Ts(10<16>)232Dn/0	involves: C3H/HeSnJ * C57BL/6JEiJ	N	17050550
MGI:3706951	M	MP:0020451	decreased sperm progressive motility	Ts(10<16>)232Dn/0	involves: C3H/HeSnJ * C57BL/6JEiJ	N	17050550
MGI:3706951	M	MP:0008261	arrest of male meiosis	Ts(10<16>)232Dn/0	involves: C3H/HeSnJ * C57BL/6JEiJ	N	17050550
MGI:3706951	M	MP:0002687	oligozoospermia	Ts(10<16>)232Dn/0	involves: C3H/HeSnJ * C57BL/6JEiJ	N	17050550
MGI:3706952	M	MP:0020451	decreased sperm progressive motility	Ts(12<17>)4Rk/0	involves: AEJ/GnRk * C3H/He * C57BL/6J * DBA/2J	N	17050550
MGI:3706952	M	MP:0004852	decreased testis weight	Ts(12<17>)4Rk/0	involves: AEJ/GnRk * C3H/He * C57BL/6J * DBA/2J	N	17050550
MGI:3706952	M	MP:0006362	abnormal male germ cell morphology	Ts(12<17>)4Rk/0	involves: AEJ/GnRk * C3H/He * C57BL/6J * DBA/2J	N	17050550
MGI:3706952	M	MP:0008261	arrest of male meiosis	Ts(12<17>)4Rk/0	involves: AEJ/GnRk * C3H/He * C57BL/6J * DBA/2J	N	17050550
MGI:3706952	M	MP:0001925	male infertility	Ts(12<17>)4Rk/0	involves: AEJ/GnRk * C3H/He * C57BL/6J * DBA/2J	N	17050550
MGI:3706952	M	MP:0002687	oligozoospermia	Ts(12<17>)4Rk/0	involves: AEJ/GnRk * C3H/He * C57BL/6J * DBA/2J	N	17050550
MGI:3706957	M	MP:0004852	decreased testis weight	Ts(4<17>)2Lws/0	involves: C3H/HeSnJ * C57BL/6J * C57BL/6JEiJ * DBA/2J	N	17050550
MGI:3706957	M	MP:0008261	arrest of male meiosis	Ts(4<17>)2Lws/0	involves: C3H/HeSnJ * C57BL/6J * C57BL/6JEiJ * DBA/2J	N	17050550
MGI:3706957	M	MP:0001925	male infertility	Ts(4<17>)2Lws/0	involves: C3H/HeSnJ * C57BL/6J * C57BL/6JEiJ * DBA/2J	N	17050550
MGI:3706957	M	MP:0006362	abnormal male germ cell morphology	Ts(4<17>)2Lws/0	involves: C3H/HeSnJ * C57BL/6J * C57BL/6JEiJ * DBA/2J	N	17050550
MGI:3706957	M	MP:0020451	decreased sperm progressive motility	Ts(4<17>)2Lws/0	involves: C3H/HeSnJ * C57BL/6J * C57BL/6JEiJ * DBA/2J	N	17050550
MGI:3706958	M	MP:0004852	decreased testis weight	Ts(16C-tel)1Cje/0	involves: C3H/HeSnJ * C57BL/6J * Rb(11.16)2H * Rb(16.17)32Lub	N	17050550
MGI:3706958	M	MP:0001922	reduced male fertility	Ts(16C-tel)1Cje/0	involves: C3H/HeSnJ * C57BL/6J * Rb(11.16)2H * Rb(16.17)32Lub	N	17050550
MGI:3706958	M	MP:0002687	oligozoospermia	Ts(16C-tel)1Cje/0	involves: C3H/HeSnJ * C57BL/6J * Rb(11.16)2H * Rb(16.17)32Lub	N	17050550
MGI:3706987	F	MP:0005668	decreased circulating leptin level	Tlr2<tm1Kir>/Tlr2<tm1Kir>	B6.129-Tlr2<tm1Kir>	N	20407745
MGI:3706987	F	MP:0009269	decreased fat cell size	Tlr2<tm1Kir>/Tlr2<tm1Kir>	B6.129-Tlr2<tm1Kir>	N	20407745
MGI:3706987	F	MP:0030016	increased adipocyte glucose uptake	Tlr2<tm1Kir>/Tlr2<tm1Kir>	B6.129-Tlr2<tm1Kir>	N	20407745
MGI:3706987	F	MP:0004889	increased energy expenditure	Tlr2<tm1Kir>/Tlr2<tm1Kir>	B6.129-Tlr2<tm1Kir>	N	20407745
MGI:3706987	F	MP:0011939	increased food intake	Tlr2<tm1Kir>/Tlr2<tm1Kir>	B6.129-Tlr2<tm1Kir>	N	20407745
MGI:3706987	F	MP:0003058	increased insulin secretion	Tlr2<tm1Kir>/Tlr2<tm1Kir>	B6.129-Tlr2<tm1Kir>	N	20407745
MGI:3706987	F	MP:0005292	improved glucose tolerance	Tlr2<tm1Kir>/Tlr2<tm1Kir>	B6.129-Tlr2<tm1Kir>	N	20407745
MGI:3706987	F	MP:0008554	decreased circulating tumor necrosis factor level	Tlr2<tm1Kir>/Tlr2<tm1Kir>	B6.129-Tlr2<tm1Kir>	N	20407745
MGI:3706987	F	MP:0009283	decreased gonadal fat pad weight	Tlr2<tm1Kir>/Tlr2<tm1Kir>	B6.129-Tlr2<tm1Kir>	N	20407745
MGI:3707122	F	MP:0001120	abnormal uterus morphology	Pten<tm1.1Hwu>/Pten<+>	involves: 129S4/SvJae * BALB/c	N	16818619
MGI:3707122	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm1.1Hwu>/Pten<+>	involves: 129S4/SvJae * BALB/c	N	16818619
MGI:3707223	M	MP:0003313	abnormal locomotor activation	Dlg3<tm1Grnt>/Y	involves: 129P2/OlaHsd * MF1	N	17344405
MGI:3707223	M	MP:0002207	abnormal long-term potentiation	Dlg3<tm1Grnt>/Y	involves: 129P2/OlaHsd * MF1	N	17344405
MGI:3707223	M	MP:0001463	abnormal spatial learning	Dlg3<tm1Grnt>/Y	involves: 129P2/OlaHsd * MF1	N	17344405
MGI:3707224	M	MP:0011089	perinatal lethality, complete penetrance	Dlg3<tm1Grnt>/Y,Dlg4<tm1Grnt>/Dlg4<tm1Grnt>	involves: 129P2/OlaHsd * MF1	N	17344405
MGI:3707225	F	MP:0011090	perinatal lethality, incomplete penetrance	Dlg3<tm1Grnt>/Dlg3<+>,Dlg4<tm1Grnt>/Dlg4<tm1Grnt>	involves: 129P2/OlaHsd * MF1	N	17344405
MGI:3707226	F	MP:0011089	perinatal lethality, complete penetrance	Dlg3<tm1Grnt>/Dlg3<tm1Grnt>,Dlg4<tm1Grnt>/Dlg4<tm1Grnt>	involves: 129P2/OlaHsd * MF1	N	17344405
MGI:3707323	M	MP:0005250	decreased Sertoli cell number	Ar<tm1Fcl>/Y	involves: 129S2/SvPas * C57BL/6	N	17360365
MGI:3707323	M	MP:0001922	reduced male fertility	Ar<tm1Fcl>/Y	involves: 129S2/SvPas * C57BL/6	N	17360365
MGI:3707323	M	MP:0004852	decreased testis weight	Ar<tm1Fcl>/Y	involves: 129S2/SvPas * C57BL/6	N	17360365
MGI:3707323	M	MP:0002209	decreased germ cell number	Ar<tm1Fcl>/Y	involves: 129S2/SvPas * C57BL/6	N	17360365
MGI:3707323	M	MP:0004929	decreased epididymis weight	Ar<tm1Fcl>/Y	involves: 129S2/SvPas * C57BL/6	N	17360365
MGI:3707323	M	MP:0031359	decreased prostate gland anterior lobe weight	Ar<tm1Fcl>/Y	involves: 129S2/SvPas * C57BL/6	N	17360365
MGI:3707323	M	MP:0001153	small seminiferous tubules	Ar<tm1Fcl>/Y	involves: 129S2/SvPas * C57BL/6	N	17360365
MGI:3707323	M	MP:0001935	decreased litter size	Ar<tm1Fcl>/Y	involves: 129S2/SvPas * C57BL/6	N	17360365
MGI:3707323	M	MP:0004910	decreased seminal vesicle weight	Ar<tm1Fcl>/Y	involves: 129S2/SvPas * C57BL/6	N	17360365
MGI:3707323	M	MP:0031362	decreased prostate gland ventral lobe weight	Ar<tm1Fcl>/Y	involves: 129S2/SvPas * C57BL/6	N	17360365
MGI:3707324	F	MP:0002169	no abnormal phenotype detected	Ar<tm1Fcl>/Ar<tm1Fcl>	involves: 129S2/SvPas * C57BL/6	N	17360365
MGI:3707365	F	MP:0012431	increased lymphoma incidence	Srpx<tm1Hzi>/Srpx<tm1Hzi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17088259
MGI:3707365	F	MP:0000691	enlarged spleen	Srpx<tm1Hzi>/Srpx<tm1Hzi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17088259
MGI:3707365	F	MP:0010264	increased hepatoma incidence	Srpx<tm1Hzi>/Srpx<tm1Hzi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17088259
MGI:3707365	F	MP:0002032	increased sarcoma incidence	Srpx<tm1Hzi>/Srpx<tm1Hzi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17088259
MGI:3707365	F	MP:0002020	increased tumor incidence	Srpx<tm1Hzi>/Srpx<tm1Hzi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17088259
MGI:3707365	F	MP:0002619	abnormal lymphocyte morphology	Srpx<tm1Hzi>/Srpx<tm1Hzi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17088259
MGI:3707365	F	MP:0002024	increased T cell derived lymphoma incidence	Srpx<tm1Hzi>/Srpx<tm1Hzi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17088259
MGI:3707365	F	MP:0002027	increased lung adenocarcinoma incidence	Srpx<tm1Hzi>/Srpx<tm1Hzi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17088259
MGI:3707366	F	MP:0012431	increased lymphoma incidence	Srpx<tm1Hzi>/Srpx<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17088259
MGI:3707368	F	MP:0001386	abnormal maternal nurturing	Rims2<tm1.1Schc>/Rims2<tm1.1Schc>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	17124501
MGI:3707400	M	MP:0008280	abnormal male germ cell apoptosis	Fasl<gld>/Fasl<gld>	B6Smn.C3-Fasl<gld>/J	N	18818293
MGI:3707400	M	MP:0030603	increased sperm number	Fasl<gld>/Fasl<gld>	B6Smn.C3-Fasl<gld>/J	N	18818293
MGI:3707426	F	MP:0001386	abnormal maternal nurturing	Mpzl3<rc>/Mpzl3<rc>	C57BL/6J-Mpzl3<rc>/J	N	15482472
MGI:3707449	M	MP:0001925	male infertility	Scmh1<tm1Hko>/Scmh1<tm1Hko>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17215307
MGI:3707449	M	MP:0020550	multinucleated giant male germ cells	Scmh1<tm1Hko>/Scmh1<tm1Hko>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17215307
MGI:3707449	M	MP:0001156	abnormal spermatogenesis	Scmh1<tm1Hko>/Scmh1<tm1Hko>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17215307
MGI:3707449	M	MP:0002216	abnormal seminiferous tubule morphology	Scmh1<tm1Hko>/Scmh1<tm1Hko>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17215307
MGI:3707449	M	MP:0001146	abnormal testis morphology	Scmh1<tm1Hko>/Scmh1<tm1Hko>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17215307
MGI:3707449	M	MP:0005159	azoospermia	Scmh1<tm1Hko>/Scmh1<tm1Hko>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17215307
MGI:3707449	M	MP:0008261	arrest of male meiosis	Scmh1<tm1Hko>/Scmh1<tm1Hko>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17215307
MGI:3707451	M	MP:0001156	abnormal spermatogenesis	Phc2<tm1Hko>/Phc2<+>,Scmh1<tm1Hko>/Scmh1<tm1Hko>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17215307
MGI:3707523	M	MP:0006400	decreased molar number	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	14506134
MGI:3707523	M	MP:0013745	abnormal eyelid margin morphology	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707523	M	MP:0001262	decreased body weight	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	14506134
MGI:3707523	M	MP:0006000	abnormal cornea epithelium morphology	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707523	M	MP:0006366	absent zigzag hairs	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	14506134
MGI:3707523	M	MP:0005287	narrow eye opening	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707523	M	MP:0002001	blindness	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	14506134
MGI:3707523	M	MP:0000577	absent eccrine glands	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	14506134
MGI:3707523	M	MP:0005251	blepharitis	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707523	M	MP:0001851	eye inflammation	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707523	M	MP:0000367	abnormal coat/ hair morphology	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	14506134
MGI:3707523	M	MP:0002001	blindness	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707523	M	MP:0001314	cornea opacity	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707523	M	MP:0000418	focal hair loss	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	14506134
MGI:3707523	M	MP:0001312	abnormal cornea morphology	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707523	M	MP:0013478	corneal limbitis	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707523	M	MP:0006236	absent Meibomian glands	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	14506134
MGI:3707523	M	MP:0001852	conjunctivitis	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707523	M	MP:0006236	absent Meibomian glands	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707523	M	MP:0002092	abnormal eye morphology	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707523	M	MP:0000417	short hair	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	14506134
MGI:3707523	M	MP:0006365	absent guard hair	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	14506134
MGI:3707523	M	MP:0001313	increased incidence of corneal inflammation	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707523	M	MP:0002060	abnormal skin morphology	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	14506134
MGI:3707523	M	MP:0003136	yellow coat color	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	14506134
MGI:3707523	M	MP:0006401	absent male preputial gland	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	14506134
MGI:3707523	M	MP:0005542	cornea vascularization	Eda<Ta-6J>/Y	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	15972955
MGI:3707524	F	MP:0009652	abnormal palatal rugae morphology	Eda<Ta-6J>/Eda<+>	C57BL/6J A<w-J>-Eda<Ta-6J>/J	N	18028050
MGI:3707536	F	MP:0005386	behavior/neurological phenotype	Aifm1<Hq>/Aifm1<+>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	Y	MGI:2387042
MGI:3707536	F	MP:0000416	sparse hair	Aifm1<Hq>/Aifm1<+>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	N	MGI:2387042
MGI:3707536	F	MP:0003631	nervous system phenotype	Aifm1<Hq>/Aifm1<+>	B6CBACa A<w-J>/A-Aifm1<Hq>/J	Y	MGI:2387042
MGI:3707539	F	MP:0005168	abnormal female meiosis	Nppc<lbab>/Nppc<lbab>	B6.PL-Nppc<lbab>/GrsrJ	N	20947764
MGI:3707557	M	MP:0001156	abnormal spermatogenesis	Egr2<tm2(cre)Pch>/?,Mnat1<tm2Tpm>/Mnat1<tm2.1Tpm>	involves: 129S2/SvPas	N	12376559
MGI:3707588	M	MP:0004852	decreased testis weight	Rad51c<tm1Sks>/Rad51c<+>	involves: 129 * C57BL/6J	N	17312021
MGI:3707590	M	MP:0002687	oligozoospermia	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	N	17312021
MGI:3707590	M	MP:0006379	abnormal spermatocyte morphology	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	N	17312021
MGI:3707590	M	MP:0001925	male infertility	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	N	17312021
MGI:3707590	F	MP:0005168	abnormal female meiosis	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	N	17312021
MGI:3707590	M	MP:0001145	abnormal male reproductive system morphology	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	N	17312021
MGI:3707590	M	MP:0002216	abnormal seminiferous tubule morphology	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	N	17312021
MGI:3707590	M	MP:0001156	abnormal spermatogenesis	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	N	17312021
MGI:3707590	F	MP:0001134	absent corpus luteum	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	N	17312021
MGI:3707590	M	MP:0008261	arrest of male meiosis	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	N	17312021
MGI:3707590	M	MP:0004852	decreased testis weight	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	N	17312021
MGI:3707590	F	MP:0001926	female infertility	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	N	17312021
MGI:3707590	F	MP:0001119	abnormal female reproductive system morphology	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	N	17312021
MGI:3707592	M	MP:0001929	abnormal gametogenesis	Paf/Y	C3H/HeSn-Paf/J	N	16467389
MGI:3707592	M	MP:0001930	abnormal meiosis	Paf/Y	C3H/HeSn-Paf/J	N	16467389
MGI:3707592	M	MP:0004218	meiotic nondisjunction during M1 phase	Paf/Y	C3H/HeSn-Paf/J	N	16467389
MGI:3707733	F	MP:0005387	immune system phenotype	Foxp3<tm2Tch>/Foxp3<+>	C.129X1-Foxp3<tm2Tch>	Y	17312141
MGI:3707734	M	MP:0005387	immune system phenotype	Foxp3<tm2Tch>/Y	C.129X1-Foxp3<tm2Tch>	Y	17312141
MGI:3707956	M	MP:0004946	abnormal regulatory T cell physiology	Foxp3<tm3Tch>/Y	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707956	M	MP:0002722	abnormal immune system organ morphology	Foxp3<tm3Tch>/Y	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707956	M	MP:0003945	abnormal lymphocyte physiology	Foxp3<tm3Tch>/Y	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707956	M	MP:0001823	thymus hypoplasia	Foxp3<tm3Tch>/Y	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707956	M	MP:0003944	abnormal T cell subpopulation ratio	Foxp3<tm3Tch>/Y	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707956	M	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology	Foxp3<tm3Tch>/Y	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707956	M	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology	Foxp3<tm3Tch>/Y	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707956	M	MP:0011085	postnatal lethality, complete penetrance	Foxp3<tm3Tch>/Y	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707956	M	MP:0005348	increased T cell proliferation	Foxp3<tm3Tch>/Y	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707956	M	MP:0000702	enlarged lymph nodes	Foxp3<tm3Tch>/Y	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707956	M	MP:0000691	enlarged spleen	Foxp3<tm3Tch>/Y	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707956	M	MP:0002816	colitis	Foxp3<tm3Tch>/Y	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707956	M	MP:0003009	abnormal cytokine secretion	Foxp3<tm3Tch>/Y	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707957	F	MP:0000715	decreased thymocyte number	Foxp3<tm3Tch>/Foxp3<+>	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707957	F	MP:0010768	mortality/aging	Foxp3<tm3Tch>/Foxp3<+>	C.129X1-Foxp3<tm3Tch>	Y	17273171
MGI:3707957	F	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology	Foxp3<tm3Tch>/Foxp3<+>	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707957	F	MP:0005018	decreased T cell number	Foxp3<tm3Tch>/Foxp3<+>	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3707957	F	MP:0006413	increased T cell apoptosis	Foxp3<tm3Tch>/Foxp3<+>	C.129X1-Foxp3<tm3Tch>	N	17273171
MGI:3708350	F	MP:0001923	reduced female fertility	Chd7<Gt(S20-7E1)Sor>/Chd7<+>	involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J	N	17334657
MGI:3708350	F	MP:0001386	abnormal maternal nurturing	Chd7<Gt(S20-7E1)Sor>/Chd7<+>	involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J	N	17334657
MGI:3708883	F	MP:0013785	abnormal mammary gland bud morphology	Lrp4<mitt>/Lrp4<mitt>	involves: C57BL/6	N	17119023
MGI:3708884	F	MP:0013785	abnormal mammary gland bud morphology	Lrp4<mte>/Lrp4<mte>	involves: C57BL/6	N	17119023
MGI:3708979	F	MP:0003570	increased uterus leiomyoma incidence	Tsc1<tm1Hin>/Tsc1<+>	involves: 129S4/SvJae * C57BL/6J	N	11438694
MGI:3709004	M	MP:0004852	decreased testis weight	Rnf212<repro57>/Rnf212<repro57>	B6;C3Fe-Rnf212<repro57>/J	N	MGI:3052828
MGI:3709004	M	MP:0001925	male infertility	Rnf212<repro57>/Rnf212<repro57>	B6;C3Fe-Rnf212<repro57>/J	N	MGI:3052828
MGI:3709004	M	MP:0005159	azoospermia	Rnf212<repro57>/Rnf212<repro57>	B6;C3Fe-Rnf212<repro57>/J	N	MGI:3052828
MGI:3709004	M	MP:0008261	arrest of male meiosis	Rnf212<repro57>/Rnf212<repro57>	B6;C3Fe-Rnf212<repro57>/J	N	MGI:3052828
MGI:3709004	M	MP:0004910	decreased seminal vesicle weight	Rnf212<repro57>/Rnf212<repro57>	B6;C3Fe-Rnf212<repro57>/J	N	MGI:3052828
MGI:3709009	M	MP:0004852	decreased testis weight	repro46/repro46	B6;C3Fe-repro46/J	N	MGI:3052828
MGI:3709009	M	MP:0004910	decreased seminal vesicle weight	repro46/repro46	B6;C3Fe-repro46/J	N	MGI:3052828
MGI:3709009	F	MP:0002016	ovary cyst	repro46/repro46	B6;C3Fe-repro46/J	N	MGI:3052828
MGI:3709009	M	MP:0005159	azoospermia	repro46/repro46	B6;C3Fe-repro46/J	N	MGI:3052828
MGI:3709009	M	MP:0001925	male infertility	repro46/repro46	B6;C3Fe-repro46/J	N	MGI:3052828
MGI:3709009	M	MP:0002216	abnormal seminiferous tubule morphology	repro46/repro46	B6;C3Fe-repro46/J	N	MGI:3052828
MGI:3709009	F	MP:0001127	small ovary	repro46/repro46	B6;C3Fe-repro46/J	N	MGI:3052828
MGI:3709009	F	MP:0001926	female infertility	repro46/repro46	B6;C3Fe-repro46/J	N	MGI:3052828
MGI:3709009	M	MP:0008261	arrest of male meiosis	repro46/repro46	B6;C3Fe-repro46/J	N	MGI:3052828
MGI:3709010	M	MP:0005159	azoospermia	repro36/repro36	B6;C3Fe-repro36/J	N	MGI:3052828
MGI:3709010	M	MP:0004852	decreased testis weight	repro36/repro36	B6;C3Fe-repro36/J	N	MGI:3052828
MGI:3709010	M	MP:0004910	decreased seminal vesicle weight	repro36/repro36	B6;C3Fe-repro36/J	N	MGI:3052828
MGI:3709010	F	MP:0001127	small ovary	repro36/repro36	B6;C3Fe-repro36/J	N	MGI:3052828
MGI:3709010	F	MP:0005431	decreased oocyte number	repro36/repro36	B6;C3Fe-repro36/J	N	MGI:3052828
MGI:3709010	M	MP:0008261	arrest of male meiosis	repro36/repro36	B6;C3Fe-repro36/J	N	MGI:3052828
MGI:3709010	M	MP:0001925	male infertility	repro36/repro36	B6;C3Fe-repro36/J	N	MGI:3052828
MGI:3709010	F	MP:0002777	absent ovarian follicles	repro36/repro36	B6;C3Fe-repro36/J	N	MGI:3052828
MGI:3709010	F	MP:0001926	female infertility	repro36/repro36	B6;C3Fe-repro36/J	N	MGI:3052828
MGI:3709014	M	MP:0001925	male infertility	Map2<repro4>/Map2<repro4>	B6;C3Fe-Map<repro4>/J	N	MGI:3052828
MGI:3709014	M	MP:0005159	azoospermia	Map2<repro4>/Map2<repro4>	B6;C3Fe-Map<repro4>/J	N	MGI:3052828
MGI:3709014	M	MP:0004852	decreased testis weight	Map2<repro4>/Map2<repro4>	B6;C3Fe-Map<repro4>/J	N	MGI:3052828
MGI:3709014	M	MP:0008261	arrest of male meiosis	Map2<repro4>/Map2<repro4>	B6;C3Fe-Map<repro4>/J	N	MGI:3052828
MGI:3709018	M	MP:0008261	arrest of male meiosis	Prdm9<repro7>/Prdm9<repro7>	B6;C3Fe-Prdm9<repro7>/J	N	MGI:3052828
MGI:3709018	M	MP:0002216	abnormal seminiferous tubule morphology	Prdm9<repro7>/Prdm9<repro7>	B6;C3Fe-Prdm9<repro7>/J	N	MGI:3052828
MGI:3709018	M	MP:0004852	decreased testis weight	Prdm9<repro7>/Prdm9<repro7>	B6;C3Fe-Prdm9<repro7>/J	N	MGI:3052828
MGI:3709018	M	MP:0001925	male infertility	Prdm9<repro7>/Prdm9<repro7>	B6;C3Fe-Prdm9<repro7>/J	N	MGI:3052828
MGI:3709018	F	MP:0001926	female infertility	Prdm9<repro7>/Prdm9<repro7>	B6;C3Fe-Prdm9<repro7>/J	N	MGI:3052828
MGI:3709018	F	MP:0001127	small ovary	Prdm9<repro7>/Prdm9<repro7>	B6;C3Fe-Prdm9<repro7>/J	N	MGI:3052828
MGI:3709018	F	MP:0002777	absent ovarian follicles	Prdm9<repro7>/Prdm9<repro7>	B6;C3Fe-Prdm9<repro7>/J	N	MGI:3052828
MGI:3709018	M	MP:0005159	azoospermia	Prdm9<repro7>/Prdm9<repro7>	B6;C3Fe-Prdm9<repro7>/J	N	MGI:3052828
MGI:3709023	F	MP:0005431	decreased oocyte number	repro14/repro14	B6;C3Fe-repro14/J	N	MGI:3052828
MGI:3709023	F	MP:0001926	female infertility	repro14/repro14	B6;C3Fe-repro14/J	N	MGI:3052828
MGI:3709023	F	MP:0001127	small ovary	repro14/repro14	B6;C3Fe-repro14/J	N	MGI:3052828
MGI:3709023	M	MP:0008261	arrest of male meiosis	repro14/repro14	B6;C3Fe-repro14/J	N	MGI:3052828
MGI:3709023	M	MP:0001925	male infertility	repro14/repro14	B6;C3Fe-repro14/J	N	MGI:3052828
MGI:3709023	M	MP:0005159	azoospermia	repro14/repro14	B6;C3Fe-repro14/J	N	MGI:3052828
MGI:3709023	M	MP:0004852	decreased testis weight	repro14/repro14	B6;C3Fe-repro14/J	N	MGI:3052828
MGI:3709023	F	MP:0002777	absent ovarian follicles	repro14/repro14	B6;C3Fe-repro14/J	N	MGI:3052828
MGI:3709031	M	MP:0001925	male infertility	Dnah1<ferf1>/Dnah1<ferf1>	B6;C3Fe-Dnah1<ferf1>/J	N	MGI:3052828
MGI:3709031	M	MP:0005389	reproductive system phenotype	Dnah1<ferf1>/Dnah1<ferf1>	B6;C3Fe-Dnah1<ferf1>/J	Y	MGI:3052828
MGI:3709031	M	MP:0009647	decreased fertilization frequency	Dnah1<ferf1>/Dnah1<ferf1>	B6;C3Fe-Dnah1<ferf1>/J	N	MGI:3052828
MGI:3709163	F	MP:0001127	small ovary	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	N	17339376
MGI:3709163	M	MP:0004852	decreased testis weight	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	N	17339376
MGI:3709163	F	MP:0005168	abnormal female meiosis	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	N	17339376
MGI:3709163	F	MP:0001926	female infertility	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	N	17339376
MGI:3709163	M	MP:0008261	arrest of male meiosis	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	N	17339376
MGI:3709163	M	MP:0001925	male infertility	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	N	17339376
MGI:3709163	M	MP:0005169	abnormal male meiosis	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	N	17339376
MGI:3709270	F	MP:0002938	white spotting	Xls/Xls<+>	CBACa.Cg-Xls/J	N	MGI:3709185
MGI:3709270	F	MP:0000421	mottled coat	Xls/Xls<+>	CBACa.Cg-Xls/J	N	MGI:3709185
MGI:3709376	F	MP:0008203	absent B-1a cells	Btk<tm1Gsv>/Btk<+>	involves: 129P2/OlaHsd * C57BL/6	N	8890160
MGI:3709376	F	MP:0005017	decreased B cell number	Btk<tm1Gsv>/Btk<+>	involves: 129P2/OlaHsd * C57BL/6	N	8890160
MGI:3709376	F	MP:0008211	decreased mature B cell number	Btk<tm1Gsv>/Btk<+>	involves: 129P2/OlaHsd * C57BL/6	N	8890160
MGI:3709377	M	MP:0008498	decreased IgG3 level	Blnk<tm1Pjln>/Blnk<tm1Pjln>,Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	15331445
MGI:3709377	M	MP:0001806	decreased IgM level	Blnk<tm1Pjln>/Blnk<tm1Pjln>,Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	15331445
MGI:3709377	M	MP:0002144	abnormal B cell differentiation	Blnk<tm1Pjln>/Blnk<tm1Pjln>,Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	15331445
MGI:3709377	M	MP:0002460	decreased immunoglobulin level	Blnk<tm1Pjln>/Blnk<tm1Pjln>,Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	15331445
MGI:3709377	M	MP:0002023	increased B cell derived lymphoma incidence	Blnk<tm1Pjln>/Blnk<tm1Pjln>,Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	15331445
MGI:3709377	M	MP:0008215	decreased immature B cell number	Blnk<tm1Pjln>/Blnk<tm1Pjln>,Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	15331445
MGI:3709377	M	MP:0008211	decreased mature B cell number	Blnk<tm1Pjln>/Blnk<tm1Pjln>,Btk<tm1Gsv>/Y	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	15331445
MGI:3709379	M	MP:0002006	neoplasm	Blnk<tm1Pjln>/Blnk<tm1Pjln>,Btk<tm1Gsv>/Y,Tg(CD19-BTK*K430R)XK24Rwhe/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6 * FVB	Y	15331445
MGI:3709379	M	MP:0001806	decreased IgM level	Blnk<tm1Pjln>/Blnk<tm1Pjln>,Btk<tm1Gsv>/Y,Tg(CD19-BTK*K430R)XK24Rwhe/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6 * FVB	N	15331445
MGI:3709379	M	MP:0002460	decreased immunoglobulin level	Blnk<tm1Pjln>/Blnk<tm1Pjln>,Btk<tm1Gsv>/Y,Tg(CD19-BTK*K430R)XK24Rwhe/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6 * FVB	N	15331445
MGI:3709379	M	MP:0002144	abnormal B cell differentiation	Blnk<tm1Pjln>/Blnk<tm1Pjln>,Btk<tm1Gsv>/Y,Tg(CD19-BTK*K430R)XK24Rwhe/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6 * FVB	N	15331445
MGI:3709379	M	MP:0008498	decreased IgG3 level	Blnk<tm1Pjln>/Blnk<tm1Pjln>,Btk<tm1Gsv>/Y,Tg(CD19-BTK*K430R)XK24Rwhe/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6 * FVB	N	15331445
MGI:3709381	M	MP:0008783	decreased B cell apoptosis	Btk<tm1Gsv>/Y,Tg(CD19-BTK*K430R)XK24Rwhe/?	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	14634110
MGI:3709381	M	MP:0002460	decreased immunoglobulin level	Btk<tm1Gsv>/Y,Tg(CD19-BTK*K430R)XK24Rwhe/?	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	14634110
MGI:3709381	M	MP:0005017	decreased B cell number	Btk<tm1Gsv>/Y,Tg(CD19-BTK*K430R)XK24Rwhe/?	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	14634110
MGI:3709381	M	MP:0000717	abnormal lymphocyte cell number	Btk<tm1Gsv>/Y,Tg(CD19-BTK*K430R)XK24Rwhe/?	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	14634110
MGI:3709381	M	MP:0005387	immune system phenotype	Btk<tm1Gsv>/Y,Tg(CD19-BTK*K430R)XK24Rwhe/?	involves: 129P2/OlaHsd * C57BL/6 * FVB	Y	15331445
MGI:3709381	M	MP:0002403	abnormal pre-B cell morphology	Btk<tm1Gsv>/Y,Tg(CD19-BTK*K430R)XK24Rwhe/?	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	14634110
MGI:3709381	M	MP:0008203	absent B-1a cells	Btk<tm1Gsv>/Y,Tg(CD19-BTK*K430R)XK24Rwhe/?	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	14634110
MGI:3709490	F	MP:0002016	ovary cyst	Pdcd4<tm1Yhcn>/Pdcd4<tm1Yhcn>	B6.129S6-Pdcd4<tm1Yhcn>	N	17114484
MGI:3709490	M	MP:0009737	prostate gland cyst	Pdcd4<tm1Yhcn>/Pdcd4<tm1Yhcn>	B6.129S6-Pdcd4<tm1Yhcn>	N	17114484
MGI:3709660	M	MP:0004852	decreased testis weight	Dedd<tm1Tmiy>/Dedd<tm1Tmiy>	B6.Cg-Dedd<tm1Tmiy>	N	17283331
MGI:3709845	M	MP:0005377	hearing/vestibular/ear phenotype	Phex<Hyp-Duk>/Y	B6.C-Phex<Hyp-Duk>/J	Y	18289812
MGI:3709845	M	MP:0005386	behavior/neurological phenotype	Phex<Hyp-Duk>/Y	B6.C-Phex<Hyp-Duk>/J	Y	18289812
MGI:3709845	M	MP:0001265	decreased body size	Phex<Hyp-Duk>/Y	B6.C-Phex<Hyp-Duk>/J	N	18289812
MGI:3709845	M	MP:0011967	increased or absent threshold for auditory brainstem response	Phex<Hyp-Duk>/Y	B6.C-Phex<Hyp-Duk>/J	N	18289812
MGI:3709845	M	MP:0000438	abnormal cranium morphology	Phex<Hyp-Duk>/Y	B6.C-Phex<Hyp-Duk>/J	N	18289812
MGI:3709845	M	MP:0000039	abnormal otic capsule morphology	Phex<Hyp-Duk>/Y	B6.C-Phex<Hyp-Duk>/J	N	18289812
MGI:3709976	F	MP:0006271	abnormal involution of the mammary gland	Zfpm2<tm1Sho>/Zfpm2<tm2Sho>,Tg(Wap-cre)11738Mam/0	involves: 129 * C57BL/6J * C57BL/6NCr	N	17310981
MGI:3709976	F	MP:0000627	abnormal mammary gland morphology	Zfpm2<tm1Sho>/Zfpm2<tm2Sho>,Tg(Wap-cre)11738Mam/0	involves: 129 * C57BL/6J * C57BL/6NCr	N	17310981
MGI:3709981	F	MP:0000609	abnormal liver physiology	Sat1<tm1Alh>/Sat1<tm1Alh>	B6.129X1-Sat1<tm1Alh>	N	17189273
MGI:3709981	F	MP:0005458	increased percent body fat/body weight	Sat1<tm1Alh>/Sat1<tm1Alh>	B6.129X1-Sat1<tm1Alh>	N	17189273
MGI:3709981	F	MP:0008908	increased total fat pad weight	Sat1<tm1Alh>/Sat1<tm1Alh>	B6.129X1-Sat1<tm1Alh>	N	17189273
MGI:3709981	F	MP:0005669	increased circulating leptin level	Sat1<tm1Alh>/Sat1<tm1Alh>	B6.129X1-Sat1<tm1Alh>	N	17189273
MGI:3709981	F	MP:0010957	abnormal aerobic respiration	Sat1<tm1Alh>/Sat1<tm1Alh>	B6.129X1-Sat1<tm1Alh>	N	17189273
MGI:3709981	F	MP:0005670	abnormal white adipose tissue physiology	Sat1<tm1Alh>/Sat1<tm1Alh>	B6.129X1-Sat1<tm1Alh>	N	17189273
MGI:3709981	F	MP:0001923	reduced female fertility	Sat1<tm1Alh>/Sat1<tm1Alh>	B6.129X1-Sat1<tm1Alh>	N	17189273
MGI:3709981	F	MP:0005455	increased susceptibility to weight gain	Sat1<tm1Alh>/Sat1<tm1Alh>	B6.129X1-Sat1<tm1Alh>	N	17189273
MGI:3709982	F	MP:0002169	no abnormal phenotype detected	Sat1<tm1Alh>/Sat1<tm1Alh>	involves: 129X1/SvJ	N	15958588
MGI:3709984	M	MP:0002052	decreased tumor incidence	Apc<Min>/Apc<Min>,Sat1<tm1Alh>/Y	involves: 129X1/SvJ * C57BL/6J	N	15958588
MGI:3710016	M	MP:0001147	small testis	Tg(MT2A-Myc)#Misu/0	C57BL/6-Tg(MT2A-Myc)#Misu	N	9077456
MGI:3710016	M	MP:0001156	abnormal spermatogenesis	Tg(MT2A-Myc)#Misu/0	C57BL/6-Tg(MT2A-Myc)#Misu	N	9077456
MGI:3710016	M	MP:0002216	abnormal seminiferous tubule morphology	Tg(MT2A-Myc)#Misu/0	C57BL/6-Tg(MT2A-Myc)#Misu	N	9077456
MGI:3710016	M	MP:0001925	male infertility	Tg(MT2A-Myc)#Misu/0	C57BL/6-Tg(MT2A-Myc)#Misu	N	9077456
MGI:3710016	M	MP:0001153	small seminiferous tubules	Tg(MT2A-Myc)#Misu/0	C57BL/6-Tg(MT2A-Myc)#Misu	N	9077456
MGI:3710016	M	MP:0004852	decreased testis weight	Tg(MT2A-Myc)#Misu/0	C57BL/6-Tg(MT2A-Myc)#Misu	N	9077456
MGI:3710016	M	MP:0005159	azoospermia	Tg(MT2A-Myc)#Misu/0	C57BL/6-Tg(MT2A-Myc)#Misu	N	9077456
MGI:3710016	M	MP:0001155	arrest of spermatogenesis	Tg(MT2A-Myc)#Misu/0	C57BL/6-Tg(MT2A-Myc)#Misu	N	9077456
MGI:3710354	F	MP:0000628	abnormal mammary gland development	Brca1<tm1Aash>/Brca1<tm1Aash>,Trp53<tm1Brd>/Trp53<+>,Tg(LGB-cre)74Acl/0	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * CBA	N	17212342
MGI:3710360	F	MP:0012106	impaired exercise endurance	Smad5<tm1Huy>/Smad5<tm1.1Huy>,Tg(Tagln-cre)1Her/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1 * SJL	N	17456754
MGI:3710360	F	MP:0005140	decreased cardiac muscle contractility	Smad5<tm1Huy>/Smad5<tm1.1Huy>,Tg(Tagln-cre)1Her/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1 * SJL	N	17456754
MGI:3710381	F	MP:0000628	abnormal mammary gland development	Tg(Wap-Tsg101)4389Kuw/0	FVB/N-Tg(Wap-Tsg101)4389Kuw	N	17369844
MGI:3710383	F	MP:0006270	abnormal mammary gland growth during lactation	Tsg101<tm1Kuw>/Tsg101<tm1Kuw>,Tg(Wap-cre)11738Mam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	17369844
MGI:3710401	F	MP:0005389	reproductive system phenotype	Taf7l<tm1.1Jw>/Taf7l<tm1.1Jw>	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	Y	17242199
MGI:3710402	M	MP:0005389	reproductive system phenotype	Taf7l<tm1.1Jw>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	Y	17242199
MGI:3710405	F	MP:0001926	female infertility	Lpin1<fld>/Lpin1<fld>	BALB/cByJ-Lpin1<fld>	N	2050689
MGI:3710405	M	MP:0001925	male infertility	Lpin1<fld>/Lpin1<fld>	BALB/cByJ-Lpin1<fld>	N	2050689
MGI:3710415	M	MP:0001146	abnormal testis morphology	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710415	M	MP:0002687	oligozoospermia	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710415	M	MP:0009295	decreased interscapular fat pad weight	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	24876128
MGI:3710415	M	MP:0005578	teratozoospermia	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710415	M	MP:0009137	decreased brown fat lipid droplet number	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	24876128
MGI:3710415	M	MP:0011699	abnormal brown adipose tissue thermogenesis	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	24876128
MGI:3710415	M	MP:0009243	hairpin sperm flagellum	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710415	M	MP:0000733	abnormal muscle development	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	24876128
MGI:3710415	M	MP:0002675	asthenozoospermia	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710415	M	MP:0006036	abnormal mitochondrial physiology	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	24876128
MGI:3710415	M	MP:0001935	decreased litter size	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710415	M	MP:0001780	decreased brown adipose tissue amount	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	24876128
MGI:3710415	M	MP:0004852	decreased testis weight	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710415	M	MP:0001929	abnormal gametogenesis	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710415	M	MP:0002971	abnormal brown adipose tissue morphology	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	24876128
MGI:3710415	M	MP:0002216	abnormal seminiferous tubule morphology	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710415	M	MP:0002106	abnormal muscle physiology	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	24876128
MGI:3710415	M	MP:0011170	abnormal brown fat cell differentiation	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	24876128
MGI:3710415	M	MP:0009237	kinked sperm flagellum	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710415	M	MP:0001922	reduced male fertility	Taf7l<tm1.1Jw>/Y	B6J.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710418	M	MP:0009237	kinked sperm flagellum	Taf7l<tm1.1Jw>/Y	129X1.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710418	M	MP:0005578	teratozoospermia	Taf7l<tm1.1Jw>/Y	129X1.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710418	M	MP:0002687	oligozoospermia	Taf7l<tm1.1Jw>/Y	129X1.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710418	M	MP:0001922	reduced male fertility	Taf7l<tm1.1Jw>/Y	129X1.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710418	M	MP:0001146	abnormal testis morphology	Taf7l<tm1.1Jw>/Y	129X1.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710418	M	MP:0004852	decreased testis weight	Taf7l<tm1.1Jw>/Y	129X1.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710418	M	MP:0001929	abnormal gametogenesis	Taf7l<tm1.1Jw>/Y	129X1.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710418	M	MP:0009243	hairpin sperm flagellum	Taf7l<tm1.1Jw>/Y	129X1.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710418	M	MP:0002216	abnormal seminiferous tubule morphology	Taf7l<tm1.1Jw>/Y	129X1.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710418	M	MP:0001935	decreased litter size	Taf7l<tm1.1Jw>/Y	129X1.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710418	M	MP:0002675	asthenozoospermia	Taf7l<tm1.1Jw>/Y	129X1.Cg-Taf7l<tm1.1Jw>	N	17242199
MGI:3710421	M	MP:0002286	cryptorchism	Dlg1<tm1Taki>/Dlg1<tm1Taki>	involves: C57BL/6 * CBA	N	17435047
MGI:3710421	M	MP:0003642	absent seminal vesicle	Dlg1<tm1Taki>/Dlg1<tm1Taki>	involves: C57BL/6 * CBA	N	17435047
MGI:3710421	F	MP:0009084	blind uterus	Dlg1<tm1Taki>/Dlg1<tm1Taki>	involves: C57BL/6 * CBA	N	17435047
MGI:3710421	F	MP:0001120	abnormal uterus morphology	Dlg1<tm1Taki>/Dlg1<tm1Taki>	involves: C57BL/6 * CBA	N	17435047
MGI:3710421	F	MP:0003535	absent vagina	Dlg1<tm1Taki>/Dlg1<tm1Taki>	involves: C57BL/6 * CBA	N	17435047
MGI:3710507	M	MP:0005389	reproductive system phenotype	Taf7l<tm1Jw>/Y	involves: 129S4/SvJae * BALB/c * C57BL/6	Y	17242199
MGI:3710508	F	MP:0005389	reproductive system phenotype	Taf7l<tm1Jw>/Taf7l<tm1Jw>	involves: 129S4/SvJae * BALB/c * C57BL/6	Y	17242199
MGI:3710594	F	MP:0005478	decreased circulating thyroxine level	Slc16a2<tm1Dgen>/Slc16a2<tm1Dgen>	either: (involves: C57BL/6N) or (involves: NMRI)	N	17318265
MGI:3710594	F	MP:0003631	nervous system phenotype	Slc16a2<tm1Dgen>/Slc16a2<tm1Dgen>	either: (involves: C57BL/6N) or (involves: NMRI)	Y	17318265
MGI:3710594	F	MP:0005480	increased circulating triiodothyronine level	Slc16a2<tm1Dgen>/Slc16a2<tm1Dgen>	either: (involves: C57BL/6N) or (involves: NMRI)	N	17318265
MGI:3710594	F	MP:0005472	abnormal triiodothyronine level	Slc16a2<tm1Dgen>/Slc16a2<tm1Dgen>	either: (involves: C57BL/6N) or (involves: NMRI)	N	17318265
MGI:3710594	F	MP:0005469	abnormal thyroxine level	Slc16a2<tm1Dgen>/Slc16a2<tm1Dgen>	either: (involves: C57BL/6N) or (involves: NMRI)	N	17318265
MGI:3710595	M	MP:0005472	abnormal triiodothyronine level	Slc16a2<tm1Dgen>/Y	either: (involves: C57BL/6N) or (involves: NMRI)	N	17318265
MGI:3710595	M	MP:0005469	abnormal thyroxine level	Slc16a2<tm1Dgen>/Y	either: (involves: C57BL/6N) or (involves: NMRI)	N	17318265
MGI:3710595	M	MP:0003631	nervous system phenotype	Slc16a2<tm1Dgen>/Y	either: (involves: C57BL/6N) or (involves: NMRI)	Y	17318265
MGI:3710595	M	MP:0005480	increased circulating triiodothyronine level	Slc16a2<tm1Dgen>/Y	either: (involves: C57BL/6N) or (involves: NMRI)	N	17318265
MGI:3710595	M	MP:0005478	decreased circulating thyroxine level	Slc16a2<tm1Dgen>/Y	either: (involves: C57BL/6N) or (involves: NMRI)	N	17318265
MGI:3710672	F	MP:0000062	increased bone mineral density	Sbmd5<AKR/J>/Sbmd5<AKR/J>	involves: AKR/J * SAMP6	N	17185055
MGI:3710673	F	MP:0000062	increased bone mineral density	Sbmd5<AKR/J>/Sbmd5<SAMP6>	involves: AKR/J * SAMP6	N	17185055
MGI:3710989	M	MP:0005188	small penis	Fkbp4<tm1Shou>/Fkbp4<tm1Shou>	involves: 129S/SvEv	N	17142810
MGI:3710989	F	MP:0001926	female infertility	Fkbp4<tm1Shou>/Fkbp4<tm1Shou>	involves: 129S/SvEv	N	17142810
MGI:3710989	M	MP:0005187	abnormal penis morphology	Fkbp4<tm1Shou>/Fkbp4<tm1Shou>	involves: 129S/SvEv	N	17142810
MGI:3710989	M	MP:0001922	reduced male fertility	Fkbp4<tm1Shou>/Fkbp4<tm1Shou>	involves: 129S/SvEv	N	17142810
MGI:3710989	M	MP:0001145	abnormal male reproductive system morphology	Fkbp4<tm1Shou>/Fkbp4<tm1Shou>	involves: 129S/SvEv	N	17142810
MGI:3710989	M	MP:0009735	abnormal prostate gland development	Fkbp4<tm1Shou>/Fkbp4<tm1Shou>	involves: 129S/SvEv	N	17142810
MGI:3710989	M	MP:0004910	decreased seminal vesicle weight	Fkbp4<tm1Shou>/Fkbp4<tm1Shou>	involves: 129S/SvEv	N	17142810
MGI:3710989	M	MP:0002674	abnormal sperm motility	Fkbp4<tm1Shou>/Fkbp4<tm1Shou>	involves: 129S/SvEv	N	17142810
MGI:3710989	M	MP:0003553	abnormal foreskin morphology	Fkbp4<tm1Shou>/Fkbp4<tm1Shou>	involves: 129S/SvEv	N	17142810
MGI:3711002	F	MP:0011091	prenatal lethality, complete penetrance	Gt(ROSA)26Sor<tm3(SS18/EGFP)Mrc>/Gt(ROSA)26Sor<tm3(SS18/EGFP)Mrc>,Hprt1<tm1(CAG-cre)Mnn>/Hprt1<tm1(CAG-cre)Mnn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17418413
MGI:3711002	F	MP:0002085	abnormal embryonic tissue morphology	Gt(ROSA)26Sor<tm3(SS18/EGFP)Mrc>/Gt(ROSA)26Sor<tm3(SS18/EGFP)Mrc>,Hprt1<tm1(CAG-cre)Mnn>/Hprt1<tm1(CAG-cre)Mnn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17418413
MGI:3711003	F	MP:0011091	prenatal lethality, complete penetrance	Gt(ROSA)26Sor<tm2(SS18)Mrc>/Gt(ROSA)26Sor<tm2(SS18)Mrc>,Hprt1<tm1(CAG-cre)Mnn>/Hprt1<tm1(CAG-cre)Mnn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17418413
MGI:3711148	M	MP:0006042	increased apoptosis	Plp1<jp-rsh>/Y	involves: C3H * C57BL/6 * STOCK Rb(1.3)1Bnr	N	17394578
MGI:3711148	M	MP:0003312	abnormal locomotor coordination	Plp1<jp-rsh>/Y	involves: C3H * C57BL/6 * STOCK Rb(1.3)1Bnr	N	17394578
MGI:3711151	M	MP:0002083	premature death	Plp1<jp-msd>/Y	involves: BALB/c * C3H * C57BL/6 * C57BL/10	N	17394578
MGI:3711151	M	MP:0006042	increased apoptosis	Plp1<jp-msd>/Y	involves: BALB/c * C3H * C57BL/6 * C57BL/10	N	17394578
MGI:3711155	M	MP:0003312	abnormal locomotor coordination	Casp12<tm1Yuan>/Casp12<tm1Yuan>,Plp1<jp-rsh>/Y	involves: 129S4/SvJae * C3H * C57BL/6 * STOCK Rb(1.3)1Bnr	N	17394578
MGI:3711155	M	MP:0006042	increased apoptosis	Casp12<tm1Yuan>/Casp12<tm1Yuan>,Plp1<jp-rsh>/Y	involves: 129S4/SvJae * C3H * C57BL/6 * STOCK Rb(1.3)1Bnr	N	17394578
MGI:3711156	M	MP:0006042	increased apoptosis	Casp12<tm1Yuan>/Casp12<tm1Yuan>,Plp1<jp-msd>/Y	involves: 129S4/SvJae * C3H * C57BL/6 * C57BL/10 * BALB/c	N	17394578
MGI:3711156	M	MP:0002083	premature death	Casp12<tm1Yuan>/Casp12<tm1Yuan>,Plp1<jp-msd>/Y	involves: 129S4/SvJae * C3H * C57BL/6 * C57BL/10 * BALB/c	N	17394578
MGI:3711227	M	MP:0001922	reduced male fertility	Slc35c1<tm1Cknr>/Slc35c1<tm1Cknr>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	N	17276979
MGI:3711227	F	MP:0001923	reduced female fertility	Slc35c1<tm1Cknr>/Slc35c1<tm1Cknr>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	N	17276979
MGI:3711227	F	MP:0001386	abnormal maternal nurturing	Slc35c1<tm1Cknr>/Slc35c1<tm1Cknr>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	N	17276979
MGI:3711235	F	MP:0001386	abnormal maternal nurturing	Cadps2<tm1Tfr>/Cadps2<tm1Tfr>	C57BL/6-Cadps2<tm1Tfr>	N	17380209
MGI:3711236	F	MP:0001386	abnormal maternal nurturing	Cadps2<tm1Tfr>/Cadps2<+>	C57BL/6-Cadps2<tm1Tfr>	N	17380209
MGI:3711278	F	MP:0004021	abnormal rod electrophysiology	Gucy2f<tm1Wbae>/Gucy2f<tm1Wbae>	involves: 129S6/SvEvTac	N	17255100
MGI:3711279	F	MP:0008449	abnormal retina cone cell outer segment morphology	Gucy2e<tm1Gar>/Gucy2e<tm1Gar>,Gucy2f<tm1Wbae>/Gucy2f<tm1Wbae>	involves: 129S6/SvEvTac	N	17255100
MGI:3711279	F	MP:0008446	decreased retina cone cell number	Gucy2e<tm1Gar>/Gucy2e<tm1Gar>,Gucy2f<tm1Wbae>/Gucy2f<tm1Wbae>	involves: 129S6/SvEvTac	N	17255100
MGI:3711279	F	MP:0001005	abnormal retina rod cell morphology	Gucy2e<tm1Gar>/Gucy2e<tm1Gar>,Gucy2f<tm1Wbae>/Gucy2f<tm1Wbae>	involves: 129S6/SvEvTac	N	17255100
MGI:3711279	F	MP:0008444	retina cone cell degeneration	Gucy2e<tm1Gar>/Gucy2e<tm1Gar>,Gucy2f<tm1Wbae>/Gucy2f<tm1Wbae>	involves: 129S6/SvEvTac	N	17255100
MGI:3711279	F	MP:0004021	abnormal rod electrophysiology	Gucy2e<tm1Gar>/Gucy2e<tm1Gar>,Gucy2f<tm1Wbae>/Gucy2f<tm1Wbae>	involves: 129S6/SvEvTac	N	17255100
MGI:3711279	F	MP:0008515	thin retina outer nuclear layer	Gucy2e<tm1Gar>/Gucy2e<tm1Gar>,Gucy2f<tm1Wbae>/Gucy2f<tm1Wbae>	involves: 129S6/SvEvTac	N	17255100
MGI:3711279	F	MP:0008587	short photoreceptor outer segment	Gucy2e<tm1Gar>/Gucy2e<tm1Gar>,Gucy2f<tm1Wbae>/Gucy2f<tm1Wbae>	involves: 129S6/SvEvTac	N	17255100
MGI:3711279	F	MP:0014336	short retina rod cell outer segment	Gucy2e<tm1Gar>/Gucy2e<tm1Gar>,Gucy2f<tm1Wbae>/Gucy2f<tm1Wbae>	involves: 129S6/SvEvTac	N	17255100
MGI:3711319	M	MP:0001168	abnormal prostate gland epithelium morphology	Psap<tm1Suz>/Psap<tm1Suz>	involves: 129P2/OlaHsd	N	11105903
MGI:3711319	M	MP:0004929	decreased epididymis weight	Psap<tm1Suz>/Psap<tm1Suz>	involves: 129P2/OlaHsd	N	11105903
MGI:3711319	M	MP:0004901	decreased male germ cell number	Psap<tm1Suz>/Psap<tm1Suz>	involves: 129P2/OlaHsd	N	11105903
MGI:3711319	M	MP:0004910	decreased seminal vesicle weight	Psap<tm1Suz>/Psap<tm1Suz>	involves: 129P2/OlaHsd	N	11105903
MGI:3711319	M	MP:0004852	decreased testis weight	Psap<tm1Suz>/Psap<tm1Suz>	involves: 129P2/OlaHsd	N	11105903
MGI:3711319	M	MP:0002631	abnormal epididymis morphology	Psap<tm1Suz>/Psap<tm1Suz>	involves: 129P2/OlaHsd	N	11105903
MGI:3711319	M	MP:0001158	abnormal prostate gland morphology	Psap<tm1Suz>/Psap<tm1Suz>	involves: 129P2/OlaHsd	N	11105903
MGI:3711319	M	MP:0002059	abnormal seminal vesicle morphology	Psap<tm1Suz>/Psap<tm1Suz>	involves: 129P2/OlaHsd	N	11105903
MGI:3711319	M	MP:0004962	decreased prostate gland weight	Psap<tm1Suz>/Psap<tm1Suz>	involves: 129P2/OlaHsd	N	11105903
MGI:3711341	M	MP:0002660	abnormal caput epididymis morphology	Lgr4<Gt(pU-21)1Kymm>/Lgr4<Gt(pU-21)1Kymm>	CBA.Cg-Lgr4<Gt(pU-21)1Kymm>	N	17079737
MGI:3711341	M	MP:0002673	abnormal sperm number	Lgr4<Gt(pU-21)1Kymm>/Lgr4<Gt(pU-21)1Kymm>	CBA.Cg-Lgr4<Gt(pU-21)1Kymm>	N	17079737
MGI:3711341	M	MP:0001925	male infertility	Lgr4<Gt(pU-21)1Kymm>/Lgr4<Gt(pU-21)1Kymm>	CBA.Cg-Lgr4<Gt(pU-21)1Kymm>	N	17079737
MGI:3711341	M	MP:0002631	abnormal epididymis morphology	Lgr4<Gt(pU-21)1Kymm>/Lgr4<Gt(pU-21)1Kymm>	CBA.Cg-Lgr4<Gt(pU-21)1Kymm>	N	17079737
MGI:3711341	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Lgr4<Gt(pU-21)1Kymm>/Lgr4<Gt(pU-21)1Kymm>	CBA.Cg-Lgr4<Gt(pU-21)1Kymm>	N	17079737
MGI:3711341	M	MP:0002675	asthenozoospermia	Lgr4<Gt(pU-21)1Kymm>/Lgr4<Gt(pU-21)1Kymm>	CBA.Cg-Lgr4<Gt(pU-21)1Kymm>	N	17079737
MGI:3711341	M	MP:0001146	abnormal testis morphology	Lgr4<Gt(pU-21)1Kymm>/Lgr4<Gt(pU-21)1Kymm>	CBA.Cg-Lgr4<Gt(pU-21)1Kymm>	N	17079737
MGI:3711341	F	MP:0001923	reduced female fertility	Lgr4<Gt(pU-21)1Kymm>/Lgr4<Gt(pU-21)1Kymm>	CBA.Cg-Lgr4<Gt(pU-21)1Kymm>	N	17079737
MGI:3711341	M	MP:0006423	dilated rete testis	Lgr4<Gt(pU-21)1Kymm>/Lgr4<Gt(pU-21)1Kymm>	CBA.Cg-Lgr4<Gt(pU-21)1Kymm>	N	17079737
MGI:3711341	M	MP:0004851	increased testis weight	Lgr4<Gt(pU-21)1Kymm>/Lgr4<Gt(pU-21)1Kymm>	CBA.Cg-Lgr4<Gt(pU-21)1Kymm>	N	17079737
MGI:3711341	M	MP:0004929	decreased epididymis weight	Lgr4<Gt(pU-21)1Kymm>/Lgr4<Gt(pU-21)1Kymm>	CBA.Cg-Lgr4<Gt(pU-21)1Kymm>	N	17079737
MGI:3711530	M	MP:0000880	decreased Purkinje cell number	Fmr1<tm1Usdn>/Y	involves: 129S6/SvEvTac * C57BL/6 * FVB	N	17442505
MGI:3711530	M	MP:0000877	abnormal Purkinje cell morphology	Fmr1<tm1Usdn>/Y	involves: 129S6/SvEvTac * C57BL/6 * FVB	N	17442505
MGI:3711530	M	MP:0003702	abnormal chromosome morphology	Fmr1<tm1Usdn>/Y	involves: 129S6/SvEvTac * C57BL/6 * FVB	N	17442505
MGI:3711533	F	MP:0001190	reddish skin	Elovl4<tm1Wked>/Elovl4<tm1Wked>	involves: 129S/SvEv * 129S1/Sv	N	17356513
MGI:3711533	F	MP:0005202	lethargy	Elovl4<tm1Wked>/Elovl4<tm1Wked>	involves: 129S/SvEv * 129S1/Sv	N	17356513
MGI:3711533	F	MP:0001240	abnormal epidermis stratum corneum morphology	Elovl4<tm1Wked>/Elovl4<tm1Wked>	involves: 129S/SvEv * 129S1/Sv	N	17356513
MGI:3711533	F	MP:0011087	neonatal lethality, complete penetrance	Elovl4<tm1Wked>/Elovl4<tm1Wked>	involves: 129S/SvEv * 129S1/Sv	N	17356513
MGI:3711533	F	MP:0002796	impaired skin barrier function	Elovl4<tm1Wked>/Elovl4<tm1Wked>	involves: 129S/SvEv * 129S1/Sv	N	17356513
MGI:3711533	F	MP:0001216	abnormal epidermal layer morphology	Elovl4<tm1Wked>/Elovl4<tm1Wked>	involves: 129S/SvEv * 129S1/Sv	N	17356513
MGI:3711534	F	MP:0004021	abnormal rod electrophysiology	Elovl4<tm1Wked>/Elovl4<+>	involves: 129S/SvEv * 129S1/Sv	N	17356513
MGI:3711534	F	MP:0005201	abnormal retina pigment epithelium morphology	Elovl4<tm1Wked>/Elovl4<+>	involves: 129S/SvEv * 129S1/Sv	N	17356513
MGI:3711534	F	MP:0002090	abnormal vision	Elovl4<tm1Wked>/Elovl4<+>	involves: 129S/SvEv * 129S1/Sv	N	17356513
MGI:3711694	M	MP:0009003	abnormal vibrissa number	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0030457	abnormal molar cusp morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5893447
MGI:3711694	M	MP:0030494	abnormal molar root morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5893447
MGI:3711694	M	MP:0004830	short incisors	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5959976
MGI:3711694	M	MP:0005358	abnormal incisor morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5959976
MGI:3711694	M	MP:0005358	abnormal incisor morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5893447
MGI:3711694	M	MP:0002277	abnormal respiratory mucosa morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	15973734
MGI:3711694	M	MP:0000577	absent eccrine glands	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	2348861
MGI:3711694	M	MP:0000367	abnormal coat/ hair morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0000585	kinked tail	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0000585	kinked tail	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5893447
MGI:3711694	M	MP:0005287	narrow eye opening	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0000572	abnormal autopod morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	2348861
MGI:3711694	M	MP:0005508	abnormal skeleton morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0006400	decreased molar number	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5959976
MGI:3711694	M	MP:0006400	decreased molar number	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5893447
MGI:3711694	M	MP:0006236	absent Meibomian glands	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0013177	abnormal tail tip morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0006402	small molars	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5959976
MGI:3711694	M	MP:0000418	focal hair loss	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5893447
MGI:3711694	M	MP:0000418	focal hair loss	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0001340	abnormal eyelid morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0002576	abnormal enamel morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5893447
MGI:3711694	M	MP:0002073	abnormal hair growth	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0013370	anhidrosis	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	2348861
MGI:3711694	M	MP:0002237	abnormal nasal cavity morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0001284	absent vibrissae	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0006370	abnormal hair follicle pheomelanosome pheomelanin content	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0006366	absent zigzag hairs	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5893447
MGI:3711694	M	MP:0006366	absent zigzag hairs	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0006365	absent guard hair	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5893447
MGI:3711694	M	MP:0000397	abnormal guard hair morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0006365	absent guard hair	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0002092	abnormal eye morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0002689	abnormal molar morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5893447
MGI:3711694	M	MP:0002132	abnormal respiratory system morphology	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0001510	abnormal coat appearance	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711694	M	MP:0000125	absent incisors	Eda<Ta>/Y	involves: A * C57BL * CBA * RIII	N	5959976
MGI:3711696	F	MP:0004381	abnormal hair follicle melanocyte morphology	Eda<Ta>/Eda<+>	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711696	F	MP:0010231	transverse fur striping	Eda<Ta>/Eda<+>	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711696	F	MP:0000367	abnormal coat/ hair morphology	Eda<Ta>/Eda<+>	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711696	F	MP:0001510	abnormal coat appearance	Eda<Ta>/Eda<+>	involves: A * C57BL * CBA * RIII	N	13103353
MGI:3711736	M	MP:0002784	abnormal Sertoli cell morphology	Dmrtc2<tm1.2Zark>/Dmrtc2<tm1.2Zark>	involves: 129S1/Sv * C57BL/6	N	17447844
MGI:3711736	M	MP:0001925	male infertility	Dmrtc2<tm1.2Zark>/Dmrtc2<tm1.2Zark>	involves: 129S1/Sv * C57BL/6	N	17447844
MGI:3711736	M	MP:0014052	increased male germ cell apoptosis	Dmrtc2<tm1.2Zark>/Dmrtc2<tm1.2Zark>	involves: 129S1/Sv * C57BL/6	N	17447844
MGI:3711736	M	MP:0001156	abnormal spermatogenesis	Dmrtc2<tm1.2Zark>/Dmrtc2<tm1.2Zark>	involves: 129S1/Sv * C57BL/6	N	17447844
MGI:3711736	M	MP:0006362	abnormal male germ cell morphology	Dmrtc2<tm1.2Zark>/Dmrtc2<tm1.2Zark>	involves: 129S1/Sv * C57BL/6	N	17447844
MGI:3711736	M	MP:0004852	decreased testis weight	Dmrtc2<tm1.2Zark>/Dmrtc2<tm1.2Zark>	involves: 129S1/Sv * C57BL/6	N	17447844
MGI:3711736	M	MP:0003830	abnormal testis development	Dmrtc2<tm1.2Zark>/Dmrtc2<tm1.2Zark>	involves: 129S1/Sv * C57BL/6	N	17447844
MGI:3711736	M	MP:0004901	decreased male germ cell number	Dmrtc2<tm1.2Zark>/Dmrtc2<tm1.2Zark>	involves: 129S1/Sv * C57BL/6	N	17447844
MGI:3711736	M	MP:0006378	abnormal spermatogonia morphology	Dmrtc2<tm1.2Zark>/Dmrtc2<tm1.2Zark>	involves: 129S1/Sv * C57BL/6	N	17447844
MGI:3711736	M	MP:0006379	abnormal spermatocyte morphology	Dmrtc2<tm1.2Zark>/Dmrtc2<tm1.2Zark>	involves: 129S1/Sv * C57BL/6	N	17447844
MGI:3711736	M	MP:0008261	arrest of male meiosis	Dmrtc2<tm1.2Zark>/Dmrtc2<tm1.2Zark>	involves: 129S1/Sv * C57BL/6	N	17447844
MGI:3711736	M	MP:0006380	abnormal spermatid morphology	Dmrtc2<tm1.2Zark>/Dmrtc2<tm1.2Zark>	involves: 129S1/Sv * C57BL/6	N	17447844
MGI:3711737	M	MP:0001147	small testis	Dmrtc2<tm1.1Zark>/Dmrtc2<tm1.1Zark>,Tg(Dhh-cre)1Mejr/0	involves: 129S1/Sv * C57BL/6	N	17447844
MGI:3711773	M	MP:0002216	abnormal seminiferous tubule morphology	Bmp4<tm1Blh>/Bmp4<+>	B6.129S2-Bmp4<tm1Blh>	N	9268572
MGI:3711773	F	MP:0001923	reduced female fertility	Bmp4<tm1Blh>/Bmp4<+>	B6.129S2-Bmp4<tm1Blh>	N	17275231
MGI:3711773	M	MP:0001145	abnormal male reproductive system morphology	Bmp4<tm1Blh>/Bmp4<+>	B6.129S2-Bmp4<tm1Blh>	N	9268572
MGI:3711773	M	MP:0001163	abnormal prostate gland anterior lobe morphology	Bmp4<tm1Blh>/Bmp4<+>	B6.129S2-Bmp4<tm1Blh>	N	9268572
MGI:3712285	M	MP:0001513	limb grasping	Mecp2<tm2Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17289941
MGI:3712285	M	MP:0001951	abnormal breathing pattern	Mecp2<tm2Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17289941
MGI:3712285	M	MP:0002083	premature death	Mecp2<tm2Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17289941
MGI:3712285	M	MP:0000745	tremors	Mecp2<tm2Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17289941
MGI:3712285	M	MP:0004924	abnormal behavior	Mecp2<tm2Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17289941
MGI:3712286	F	MP:0004924	abnormal behavior	Mecp2<tm2Bird>/Mecp2<+>	involves: 129P2/OlaHsd * C57BL/6	N	17289941
MGI:3712286	F	MP:0001261	obese	Mecp2<tm2Bird>/Mecp2<+>	involves: 129P2/OlaHsd * C57BL/6	N	17289941
MGI:3712286	F	MP:0001951	abnormal breathing pattern	Mecp2<tm2Bird>/Mecp2<+>	involves: 129P2/OlaHsd * C57BL/6	N	17289941
MGI:3712286	F	MP:0000745	tremors	Mecp2<tm2Bird>/Mecp2<+>	involves: 129P2/OlaHsd * C57BL/6	N	17289941
MGI:3712286	F	MP:0001513	limb grasping	Mecp2<tm2Bird>/Mecp2<+>	involves: 129P2/OlaHsd * C57BL/6	N	17289941
MGI:3712286	F	MP:0001473	reduced long-term potentiation	Mecp2<tm2Bird>/Mecp2<+>	involves: 129P2/OlaHsd * C57BL/6	N	17289941
MGI:3712287	F	MP:0001951	abnormal breathing pattern	Mecp2<tm2Bird>/Mecp2<+>,Tg(CAG-cre/Esr1*)5Amc/?	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	17289941
MGI:3712287	F	MP:0001473	reduced long-term potentiation	Mecp2<tm2Bird>/Mecp2<+>,Tg(CAG-cre/Esr1*)5Amc/?	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	17289941
MGI:3712287	F	MP:0000745	tremors	Mecp2<tm2Bird>/Mecp2<+>,Tg(CAG-cre/Esr1*)5Amc/?	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	17289941
MGI:3712287	F	MP:0004924	abnormal behavior	Mecp2<tm2Bird>/Mecp2<+>,Tg(CAG-cre/Esr1*)5Amc/?	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	17289941
MGI:3712287	F	MP:0001513	limb grasping	Mecp2<tm2Bird>/Mecp2<+>,Tg(CAG-cre/Esr1*)5Amc/?	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	17289941
MGI:3712287	F	MP:0001261	obese	Mecp2<tm2Bird>/Mecp2<+>,Tg(CAG-cre/Esr1*)5Amc/?	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	17289941
MGI:3712449	F	MP:0006269	abnormal mammary gland growth during pregnancy	Tg(WapNotch4)10Rnc/0	involves: FVB/N	N	8620493
MGI:3712449	F	MP:0010249	lactation failure	Tg(WapNotch4)10Rnc/0	involves: FVB/N	N	8620493
MGI:3712450	M	MP:0002006	neoplasm	Tg(WapNotch4)10Rnc/Y	involves: FVB/N	Y	8620493
MGI:3712657	M	MP:0006058	decreased cerebral infarct size	Cd40lg<tm1Imx>/Y	B6.129S2-Cd40lg<tm1Imx>/J	N	15795333
MGI:3712657	M	MP:0003628	abnormal leukocyte adhesion	Cd40lg<tm1Imx>/Y	B6.129S2-Cd40lg<tm1Imx>/J	N	15795333
MGI:3712657	M	MP:0009549	decreased platelet aggregation	Cd40lg<tm1Imx>/Y	B6.129S2-Cd40lg<tm1Imx>/J	N	15795333
MGI:3712657	M	MP:0000832	abnormal thalamus morphology	Cd40lg<tm1Imx>/Y	B6.129S2-Cd40lg<tm1Imx>/J	N	15885854
MGI:3712666	F	MP:0005364	increased susceptibility to prion infection	Cd40lg<tm1Imx>/Cd40lg<tm1Imx>	involves: 129S2/SvPas * C57BL/6	N	15071493
MGI:3712666	F	MP:0003241	loss of cortex neurons	Cd40lg<tm1Imx>/Cd40lg<tm1Imx>	involves: 129S2/SvPas * C57BL/6	N	15071493
MGI:3712666	F	MP:0008918	microgliosis	Cd40lg<tm1Imx>/Cd40lg<tm1Imx>	involves: 129S2/SvPas * C57BL/6	N	15071493
MGI:3712666	F	MP:0002654	spongiform encephalopathy	Cd40lg<tm1Imx>/Cd40lg<tm1Imx>	involves: 129S2/SvPas * C57BL/6	N	15071493
MGI:3712666	F	MP:0002229	neurodegeneration	Cd40lg<tm1Imx>/Cd40lg<tm1Imx>	involves: 129S2/SvPas * C57BL/6	N	15071493
MGI:3712666	F	MP:0005389	reproductive system phenotype	Cd40lg<tm1Imx>/Cd40lg<tm1Imx>	involves: 129S2/SvPas * C57BL/6	Y	7964465
MGI:3712666	F	MP:0002551	abnormal blood coagulation	Cd40lg<tm1Imx>/Cd40lg<tm1Imx>	involves: 129S2/SvPas * C57BL/6	N	11875495
MGI:3712666	F	MP:0003633	abnormal nervous system physiology	Cd40lg<tm1Imx>/Cd40lg<tm1Imx>	involves: 129S2/SvPas * C57BL/6	N	15071493
MGI:3712670	M	MP:0002216	abnormal seminiferous tubule morphology	Piwil4<tm1Ghan>/Piwil4<tm1Ghan>	involves: 129S7/SvEvBrd * C57BL/6	N	17395546
MGI:3712670	M	MP:0004901	decreased male germ cell number	Piwil4<tm1Ghan>/Piwil4<tm1Ghan>	involves: 129S7/SvEvBrd * C57BL/6	N	17395546
MGI:3712670	M	MP:0001147	small testis	Piwil4<tm1Ghan>/Piwil4<tm1Ghan>	involves: 129S7/SvEvBrd * C57BL/6	N	17395546
MGI:3712670	M	MP:0001922	reduced male fertility	Piwil4<tm1Ghan>/Piwil4<tm1Ghan>	involves: 129S7/SvEvBrd * C57BL/6	N	17395546
MGI:3712670	M	MP:0008261	arrest of male meiosis	Piwil4<tm1Ghan>/Piwil4<tm1Ghan>	involves: 129S7/SvEvBrd * C57BL/6	N	17395546
MGI:3712670	M	MP:0006379	abnormal spermatocyte morphology	Piwil4<tm1Ghan>/Piwil4<tm1Ghan>	involves: 129S7/SvEvBrd * C57BL/6	N	17395546
MGI:3712949	M	MP:0002675	asthenozoospermia	Slc26a4<pdsm>/Slc26a4<pdsm>	BXA7/PgnJ-Slc26a4<pdsm>/J	N	MGI:3712813
MGI:3712949	M	MP:0003205	testicular atrophy	Slc26a4<pdsm>/Slc26a4<pdsm>	BXA7/PgnJ-Slc26a4<pdsm>/J	N	MGI:3712813
MGI:3712949	M	MP:0002687	oligozoospermia	Slc26a4<pdsm>/Slc26a4<pdsm>	BXA7/PgnJ-Slc26a4<pdsm>/J	N	MGI:3712813
MGI:3712953	F	MP:0001926	female infertility	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Lin9<tm1Orc>/Lin9<tm1Orc>	involves: 129S1/Sv	N	16730350
MGI:3712953	M	MP:0001925	male infertility	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Lin9<tm1Orc>/Lin9<tm1Orc>	involves: 129S1/Sv	N	16730350
MGI:3712954	F	MP:0001926	female infertility	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv	N	16730350
MGI:3712954	M	MP:0002785	absent Leydig cells	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv	N	16730350
MGI:3712954	M	MP:0001925	male infertility	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv	N	16730350
MGI:3712954	M	MP:0005159	azoospermia	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv	N	16730350
MGI:3712981	F	MP:0002294	short gestation period	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	N	10731669
MGI:3713124	M	MP:0002163	abnormal gland morphology	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	14506134
MGI:3713124	M	MP:0013373	increased sebum secretion	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	14506134
MGI:3713124	M	MP:0005387	immune system phenotype	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	Y	15972955
MGI:3713124	M	MP:0002073	abnormal hair growth	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	14506134
MGI:3713124	M	MP:0006236	absent Meibomian glands	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	15972955
MGI:3713124	M	MP:0013378	increased sebocyte number	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	14506134
MGI:3713124	M	MP:0001511	disheveled coat	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	14506134
MGI:3713124	M	MP:0002717	abnormal male preputial gland morphology	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	14506134
MGI:3713124	M	MP:0002060	abnormal skin morphology	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	14506134
MGI:3713124	M	MP:0001262	decreased body weight	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	14506134
MGI:3713124	M	MP:0006236	absent Meibomian glands	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	14506134
MGI:3713124	M	MP:0009793	sebaceous gland hypertrophy	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	15972955
MGI:3713124	M	MP:0006366	absent zigzag hairs	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	14506134
MGI:3713124	M	MP:0000417	short hair	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	14506134
MGI:3713124	M	MP:0000367	abnormal coat/ hair morphology	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	14506134
MGI:3713124	M	MP:0009794	sebaceous gland hyperplasia	Eda<Ta-6J>/Y,Tg(MMTVtTA)1Mam/0,Tg(tetO-Eda*A1)1Dsch/0	involves: C57BL/6J	N	14506134
MGI:3713237	M	MP:0011088	neonatal lethality, incomplete penetrance	Efnb1<tm1Rha>/Y	involves: 129P2/OlaHsd	N	12919674
MGI:3713237	M	MP:0000111	cleft palate	Efnb1<tm1Rha>/Y	involves: 129P2/OlaHsd	N	12919674
MGI:3713238	F	MP:0000155	asymmetric rib joints	Efnb1<tm1Rha>/Efnb1<+>	involves: 129P2/OlaHsd	N	12919674
MGI:3713238	F	MP:0010082	sternebra fusion	Efnb1<tm1Rha>/Efnb1<+>	involves: 129P2/OlaHsd	N	12919674
MGI:3713238	F	MP:0009743	preaxial polydactyly	Efnb1<tm1Rha>/Efnb1<+>	involves: 129P2/OlaHsd	N	12919674
MGI:3713239	F	MP:0000111	cleft palate	Efnb1<tm1Rha>/Efnb1<tm1Rha>	involves: 129P2/OlaHsd	N	12919674
MGI:3713239	F	MP:0011088	neonatal lethality, incomplete penetrance	Efnb1<tm1Rha>/Efnb1<tm1Rha>	involves: 129P2/OlaHsd	N	12919674
MGI:3713240	M	MP:0004321	short sternum	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0005389	reproductive system phenotype	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	Y	12919674
MGI:3713240	M	MP:0008915	fused carpal bones	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0010082	sternebra fusion	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0000164	abnormal cartilage development	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0011086	postnatal lethality, incomplete penetrance	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0000562	polydactyly	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0002114	abnormal axial skeleton morphology	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0003052	omphalocele	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0004322	abnormal sternebra morphology	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0008146	asymmetric sternocostal joints	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0000554	abnormal carpal bone morphology	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0000572	abnormal autopod morphology	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0000111	cleft palate	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0004083	polysyndactyly	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0008271	abnormal bone ossification	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0001785	edema	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713240	M	MP:0008525	decreased cranium height	Efnb1<tm1Rha>/Y,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713241	F	MP:0000164	abnormal cartilage development	Efnb1<tm1Rha>/Efnb1<+>,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713241	F	MP:0008915	fused carpal bones	Efnb1<tm1Rha>/Efnb1<+>,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713241	F	MP:0000562	polydactyly	Efnb1<tm1Rha>/Efnb1<+>,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713241	F	MP:0000554	abnormal carpal bone morphology	Efnb1<tm1Rha>/Efnb1<+>,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713241	F	MP:0011086	postnatal lethality, incomplete penetrance	Efnb1<tm1Rha>/Efnb1<+>,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713241	F	MP:0000155	asymmetric rib joints	Efnb1<tm1Rha>/Efnb1<+>,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713241	F	MP:0003052	omphalocele	Efnb1<tm1Rha>/Efnb1<+>,Tg(Pgk1-cre)1Lni/?	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713243	F	MP:0001785	edema	Efnb1<tm1.1Rha>/Efnb1<tm1.1Rha>	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713243	F	MP:0000111	cleft palate	Efnb1<tm1.1Rha>/Efnb1<tm1.1Rha>	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713243	F	MP:0008525	decreased cranium height	Efnb1<tm1.1Rha>/Efnb1<tm1.1Rha>	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713243	F	MP:0011088	neonatal lethality, incomplete penetrance	Efnb1<tm1.1Rha>/Efnb1<tm1.1Rha>	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713243	F	MP:0003052	omphalocele	Efnb1<tm1.1Rha>/Efnb1<tm1.1Rha>	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	12919674
MGI:3713244	F	MP:0000562	polydactyly	Efnb1<tm1Rha>/Efnb1<+>,Tg(Prrx1-cre)1Cjt/?	involves: 129P2/OlaHsd * C57BL/6J * SJL/J	N	12919674
MGI:3713273	F	MP:0013719	pale mammary gland	Mrtfa<tm1Eno>/Mrtfa<tm1Eno>	involves: 129S/SvEv * C57BL/6	N	16847332
MGI:3713273	F	MP:0001882	abnormal lactation	Mrtfa<tm1Eno>/Mrtfa<tm1Eno>	involves: 129S/SvEv * C57BL/6	N	16847332
MGI:3713273	F	MP:0013718	galactostasis	Mrtfa<tm1Eno>/Mrtfa<tm1Eno>	involves: 129S/SvEv * C57BL/6	N	16847332
MGI:3713273	F	MP:0006270	abnormal mammary gland growth during lactation	Mrtfa<tm1Eno>/Mrtfa<tm1Eno>	involves: 129S/SvEv * C57BL/6	N	16847332
MGI:3713273	F	MP:0013778	abnormal mammary gland myoepithelium morphology	Mrtfa<tm1Eno>/Mrtfa<tm1Eno>	involves: 129S/SvEv * C57BL/6	N	16847332
MGI:3713273	F	MP:0013779	abnormal mammary gland myoepithelium physiology	Mrtfa<tm1Eno>/Mrtfa<tm1Eno>	involves: 129S/SvEv * C57BL/6	N	16847332
MGI:3713273	F	MP:0014126	increased mammary gland apoptosis	Mrtfa<tm1Eno>/Mrtfa<tm1Eno>	involves: 129S/SvEv * C57BL/6	N	16847332
MGI:3713273	F	MP:0006271	abnormal involution of the mammary gland	Mrtfa<tm1Eno>/Mrtfa<tm1Eno>	involves: 129S/SvEv * C57BL/6	N	16847332
MGI:3713529	F	MP:0001384	abnormal pup retrieval	Gabrd<tm1Geh>/Gabrd<tm1Geh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18667149
MGI:3713529	F	MP:0001386	abnormal maternal nurturing	Gabrd<tm1Geh>/Gabrd<tm1Geh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18667149
MGI:3713529	F	MP:0001385	pup cannibalization	Gabrd<tm1Geh>/Gabrd<tm1Geh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18667149
MGI:3713670	F	MP:0003355	decreased ovulation rate	Hr<rh-Y>/Hr<rh-Y>	involves: B10.R109/Y * C57BL/10SnY	N	9832316
MGI:3713670	F	MP:0001926	female infertility	Hr<rh-Y>/Hr<rh-Y>	involves: B10.R109/Y * C57BL/10SnY	N	9832316
MGI:3713699	M	MP:0001922	reduced male fertility	Adamtsl2<stb>/Adamtsl2<stb>	Not Specified	N	5713631
MGI:3713699	M	MP:0002673	abnormal sperm number	Adamtsl2<stb>/Adamtsl2<stb>	Not Specified	N	5713631
MGI:3713699	M	MP:0001147	small testis	Adamtsl2<stb>/Adamtsl2<stb>	Not Specified	N	5713631
MGI:3713748	M	MP:0004543	abnormal sperm physiology	Atp2b4<tm1Ksch>/Atp2b4<tm1Ksch>	involves: 129P2/OlaHsd * C57BL/6	N	15078889
MGI:3713748	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Atp2b4<tm1Ksch>/Atp2b4<tm1Ksch>	involves: 129P2/OlaHsd * C57BL/6	N	28714864
MGI:3713748	M	MP:0002675	asthenozoospermia	Atp2b4<tm1Ksch>/Atp2b4<tm1Ksch>	involves: 129P2/OlaHsd * C57BL/6	N	15078889
MGI:3713748	M	MP:0001925	male infertility	Atp2b4<tm1Ksch>/Atp2b4<tm1Ksch>	involves: 129P2/OlaHsd * C57BL/6	N	15078889
MGI:3713751	F	MP:0000662	abnormal branching of the mammary ductal tree	Sirt1<tm1.1Ygu>/Sirt1<tm1.1Ygu>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	17201918
MGI:3713751	F	MP:0000627	abnormal mammary gland morphology	Sirt1<tm1.1Ygu>/Sirt1<tm1.1Ygu>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	17201918
MGI:3713751	F	MP:0013716	hypolactation	Sirt1<tm1.1Ygu>/Sirt1<tm1.1Ygu>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	17201918
MGI:3713751	F	MP:0006269	abnormal mammary gland growth during pregnancy	Sirt1<tm1.1Ygu>/Sirt1<tm1.1Ygu>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	17201918
MGI:3713773	M	MP:0003546	decreased alcohol consumption	Gria3<tm1.1Rsp>/Y	B6.129-Gria3<tm1.1Rsp>	N	16436610
MGI:3713773	M	MP:0001405	impaired coordination	Gria3<tm1.1Rsp>/Y	B6.129-Gria3<tm1.1Rsp>	N	16436610
MGI:3713773	M	MP:0003313	abnormal locomotor activation	Gria3<tm1.1Rsp>/Y	B6.129-Gria3<tm1.1Rsp>	N	16436610
MGI:3713780	F	MP:0001132	absent mature ovarian follicles	Ewsr1<tm1Sblee>/Ewsr1<tm1Sblee>	involves: 129S6/SvEvTac * Black Swiss	N	17415412
MGI:3713780	F	MP:0001127	small ovary	Ewsr1<tm1Sblee>/Ewsr1<tm1Sblee>	involves: 129S6/SvEvTac * Black Swiss	N	17415412
MGI:3713780	F	MP:0001926	female infertility	Ewsr1<tm1Sblee>/Ewsr1<tm1Sblee>	involves: 129S6/SvEvTac * Black Swiss	N	17415412
MGI:3713780	F	MP:0001126	abnormal ovary morphology	Ewsr1<tm1Sblee>/Ewsr1<tm1Sblee>	involves: 129S6/SvEvTac * Black Swiss	N	17415412
MGI:3713780	M	MP:0001925	male infertility	Ewsr1<tm1Sblee>/Ewsr1<tm1Sblee>	involves: 129S6/SvEvTac * Black Swiss	N	17415412
MGI:3713780	F	MP:0001134	absent corpus luteum	Ewsr1<tm1Sblee>/Ewsr1<tm1Sblee>	involves: 129S6/SvEvTac * Black Swiss	N	17415412
MGI:3713780	M	MP:0006380	abnormal spermatid morphology	Ewsr1<tm1Sblee>/Ewsr1<tm1Sblee>	involves: 129S6/SvEvTac * Black Swiss	N	17415412
MGI:3713780	M	MP:0001147	small testis	Ewsr1<tm1Sblee>/Ewsr1<tm1Sblee>	involves: 129S6/SvEvTac * Black Swiss	N	17415412
MGI:3713780	M	MP:0005169	abnormal male meiosis	Ewsr1<tm1Sblee>/Ewsr1<tm1Sblee>	involves: 129S6/SvEvTac * Black Swiss	N	17415412
MGI:3713780	M	MP:0001146	abnormal testis morphology	Ewsr1<tm1Sblee>/Ewsr1<tm1Sblee>	involves: 129S6/SvEvTac * Black Swiss	N	17415412
MGI:3713780	M	MP:0006379	abnormal spermatocyte morphology	Ewsr1<tm1Sblee>/Ewsr1<tm1Sblee>	involves: 129S6/SvEvTac * Black Swiss	N	17415412
MGI:3713797	F	MP:0009433	polyovular ovarian follicle	Irs2<tm1.1With>/Irs2<tm1.1With>	B6.129S6-Irs2<tm1.1With>	N	17329594
MGI:3713797	F	MP:0011129	decreased tertiary ovarian follicle number	Irs2<tm1.1With>/Irs2<tm1.1With>	B6.129S6-Irs2<tm1.1With>	N	17329594
MGI:3713797	F	MP:0001130	abnormal ovarian folliculogenesis	Irs2<tm1.1With>/Irs2<tm1.1With>	B6.129S6-Irs2<tm1.1With>	N	17329594
MGI:3713797	F	MP:0002679	abnormal corpus luteum morphology	Irs2<tm1.1With>/Irs2<tm1.1With>	B6.129S6-Irs2<tm1.1With>	N	17329594
MGI:3713797	F	MP:0001131	abnormal ovarian follicle morphology	Irs2<tm1.1With>/Irs2<tm1.1With>	B6.129S6-Irs2<tm1.1With>	N	17329594
MGI:3713797	F	MP:0001132	absent mature ovarian follicles	Irs2<tm1.1With>/Irs2<tm1.1With>	B6.129S6-Irs2<tm1.1With>	N	17329594
MGI:3713797	F	MP:0031239	increased atretic ovarian follicle number	Irs2<tm1.1With>/Irs2<tm1.1With>	B6.129S6-Irs2<tm1.1With>	N	17329594
MGI:3713797	F	MP:0031018	decreased granulosa cell proliferation	Irs2<tm1.1With>/Irs2<tm1.1With>	B6.129S6-Irs2<tm1.1With>	N	17329594
MGI:3713798	F	MP:0009006	prolonged estrous cycle	Irs2<tm1With>/Irs2<tm1With>,Tg(Nes-cre)1Kln/?	involves: 129S6/SvEvTac * C57BL/6 * SJL	N	17329594
MGI:3713798	F	MP:0009011	prolonged diestrus	Irs2<tm1With>/Irs2<tm1With>,Tg(Nes-cre)1Kln/?	involves: 129S6/SvEvTac * C57BL/6 * SJL	N	17329594
MGI:3713817	M	MP:0005565	increased blood urea nitrogen level	Gne<tm1Dar>/Gne<tm1Dar>	involves: C57BL/6J	N	17549255
MGI:3713861	M	MP:0004852	decreased testis weight	Adipor2<tm1Dgen>/Adipor2<tm1Dgen>	B6.129P2-Adipor2<tm1Dgen>	N	17327425
MGI:3714054	F	MP:0001131	abnormal ovarian follicle morphology	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/?	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	N	17374637
MGI:3714054	F	MP:0005431	decreased oocyte number	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/?	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	N	17374637
MGI:3714054	F	MP:0001923	reduced female fertility	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/?	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	N	17374637
MGI:3714055	F	MP:0009375	thin zona pellucida	C1galt1<tm1.2Rpmc>/C1galt1<tm1.2Rpmc>	involves: 129S1/Sv * 129S1/SvImJ * C57BL/6	N	17374637
MGI:3714055	F	MP:0003696	abnormal zona pellucida morphology	C1galt1<tm1.2Rpmc>/C1galt1<tm1.2Rpmc>	involves: 129S1/Sv * 129S1/SvImJ * C57BL/6	N	17374637
MGI:3714071	M	MP:0001925	male infertility	Etl4<Gt(6LSN)6029Gos>/Etl4<Gt(6LSN)6029Gos>,Etn2<Sd>/Etn2<+>	involves: 129/Sv * 129S2/SvPas * C57BL/6 * NMRI	N	9706697
MGI:3714371	F	MP:0009505	abnormal mammary gland lobule morphology	Erbb2<tm8(Erbb2)Mul>/Erbb2<+>,Tg(MMTV-cre)7Mul/?	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	15051890
MGI:3714371	F	MP:0000628	abnormal mammary gland development	Erbb2<tm8(Erbb2)Mul>/Erbb2<+>,Tg(MMTV-cre)7Mul/?	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	10716706
MGI:3714392	M	MP:0001925	male infertility	Cacnb4<lh-4J>/Cacnb4<lh-4J>	C3Fe(SWV)-Cacnb4<lh-4J>/GrsrJ	N	MGI:3712358
MGI:3714515	F	MP:0001385	pup cannibalization	Nkd1<tm1Kwha>/Nkd1<+>,Nkd2<tm1Kwha>/Nkd2<+>	involves: 129S/SvEv * C57BL/6	N	17438140
MGI:3714516	F	MP:0001385	pup cannibalization	Nkd1<tm1Kwha>/Nkd1<tm1Kwha>,Nkd2<tm1Kwha>/Nkd2<tm1Kwha>	involves: 129S/SvEv * C57BL/6	N	17438140
MGI:3714601	F	MP:0002676	uterus hyperplasia	Del(4D4Mit190-D4Mit51)2Aam/+	involves: 129S7/SvEvBrd	N	17289567
MGI:3714770	M	MP:0003415	priapism	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0005591	decreased vasodilation	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0005011	increased eosinophil cell number	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0005013	increased lymphocyte cell number	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0001157	small seminal vesicle	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	16847346
MGI:3714770	M	MP:0003957	abnormal nitric oxide homeostasis	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0031214	hypercoagulability	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0000218	increased leukocyte cell number	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0031158	abnormal venous thrombosis	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0003786	premature aging	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0000219	increased neutrophil cell number	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0005416	abnormal circulating protein level	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0020332	impaired leukocyte tethering or rolling	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0008254	increased megakaryocyte cell number	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0012329	increased circulating factor VIII level	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0012331	increased circulating fibrinogen level	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0031121	increased susceptibility to induced thrombosis	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0005595	abnormal vascular smooth muscle physiology	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0003025	increased vasoconstriction	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0005489	vascular smooth muscle hyperplasia	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0005505	thrombocytosis	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0002607	decreased basophil cell number	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	21799179
MGI:3714770	M	MP:0004852	decreased testis weight	Bmal1<tm1Bra>/Bmal1<tm1Bra>	B6.129-Bmal1<tm1Bra>	N	16847346
MGI:3715159	F	MP:0005370	liver/biliary system phenotype	Hprt1<tm1(UBC-UBB)Rrk>/Hprt1<tm1(UBC-UBB)Rrk>,Ubc<tm1Rrk>/Ubc<tm1Rrk>	involves: 129 * C57BL/6J	Y	17491588
MGI:3715159	F	MP:0011089	perinatal lethality, complete penetrance	Hprt1<tm1(UBC-UBB)Rrk>/Hprt1<tm1(UBC-UBB)Rrk>,Ubc<tm1Rrk>/Ubc<tm1Rrk>	involves: 129 * C57BL/6J	N	17491588
MGI:3715159	F	MP:0001698	decreased embryo size	Hprt1<tm1(UBC-UBB)Rrk>/Hprt1<tm1(UBC-UBB)Rrk>,Ubc<tm1Rrk>/Ubc<tm1Rrk>	involves: 129 * C57BL/6J	N	17491588
MGI:3715159	F	MP:0005384	cellular phenotype	Hprt1<tm1(UBC-UBB)Rrk>/Hprt1<tm1(UBC-UBB)Rrk>,Ubc<tm1Rrk>/Ubc<tm1Rrk>	involves: 129 * C57BL/6J	Y	17491588
MGI:3715160	M	MP:0001698	decreased embryo size	Hprt1<tm1(UBC-UBB)Rrk>/Y,Ubc<tm1Rrk>/Ubc<tm1Rrk>	involves: 129 * C57BL/6J	N	17491588
MGI:3715160	M	MP:0011089	perinatal lethality, complete penetrance	Hprt1<tm1(UBC-UBB)Rrk>/Y,Ubc<tm1Rrk>/Ubc<tm1Rrk>	involves: 129 * C57BL/6J	N	17491588
MGI:3715160	M	MP:0005384	cellular phenotype	Hprt1<tm1(UBC-UBB)Rrk>/Y,Ubc<tm1Rrk>/Ubc<tm1Rrk>	involves: 129 * C57BL/6J	Y	17491588
MGI:3715160	M	MP:0005370	liver/biliary system phenotype	Hprt1<tm1(UBC-UBB)Rrk>/Y,Ubc<tm1Rrk>/Ubc<tm1Rrk>	involves: 129 * C57BL/6J	Y	17491588
MGI:3715234	M	MP:0002169	no abnormal phenotype detected	Cdx4<tm1Jdes>/Y	involves: C57BL/6 * FVB	N	16396910
MGI:3715363	F	MP:0002073	abnormal hair growth	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0003704	abnormal hair follicle development	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0012078	abnormal tail ring morphology	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0000585	kinked tail	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0002095	abnormal skin pigmentation	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0013580	abnormal nasal gland morphology	Eda<Ta>/Eda<Ta>	Not Specified	N	27590203
MGI:3715363	F	MP:0013582	abnormal lateral nasal gland morphology	Eda<Ta>/Eda<Ta>	Not Specified	N	27590203
MGI:3715363	F	MP:0006365	absent guard hair	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0006366	absent zigzag hairs	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0006371	absent hair follicle pheomelanosome pheomelanin	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0010233	hairless tail	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0009003	abnormal vibrissa number	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0005287	narrow eye opening	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0002074	abnormal hair texture	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0002233	abnormal nose morphology	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0001199	thin skin	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0002237	abnormal nasal cavity morphology	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715363	F	MP:0000367	abnormal coat/ hair morphology	Eda<Ta>/Eda<Ta>	Not Specified	N	13103353
MGI:3715465	F	MP:0001923	reduced female fertility	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * NIH Black Swiss	N	11734632
MGI:3715465	M	MP:0001922	reduced male fertility	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * NIH Black Swiss	N	11734632
MGI:3715612	M	MP:0006362	abnormal male germ cell morphology	Clcn2<tm1Tjj>/Clcn2<tm1Tjj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11250895
MGI:3715612	M	MP:0001925	male infertility	Clcn2<tm1Tjj>/Clcn2<tm1Tjj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11250895
MGI:3715612	M	MP:0001154	seminiferous tubule degeneration	Clcn2<tm1Tjj>/Clcn2<tm1Tjj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11250895
MGI:3715612	M	MP:0013600	testis degeneration	Clcn2<tm1Tjj>/Clcn2<tm1Tjj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	31727896
MGI:3715612	M	MP:0004109	abnormal Sertoli cell development	Clcn2<tm1Tjj>/Clcn2<tm1Tjj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11250895
MGI:3715612	M	MP:0001147	small testis	Clcn2<tm1Tjj>/Clcn2<tm1Tjj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11250895
MGI:3715612	M	MP:0002784	abnormal Sertoli cell morphology	Clcn2<tm1Tjj>/Clcn2<tm1Tjj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11250895
MGI:3715612	M	MP:0001152	increased Leydig cell number	Clcn2<tm1Tjj>/Clcn2<tm1Tjj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11250895
MGI:3715612	M	MP:0003830	abnormal testis development	Clcn2<tm1Tjj>/Clcn2<tm1Tjj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11250895
MGI:3715612	M	MP:0006379	abnormal spermatocyte morphology	Clcn2<tm1Tjj>/Clcn2<tm1Tjj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11250895
MGI:3715612	M	MP:0005159	azoospermia	Clcn2<tm1Tjj>/Clcn2<tm1Tjj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11250895
MGI:3715612	M	MP:0002216	abnormal seminiferous tubule morphology	Clcn2<tm1Tjj>/Clcn2<tm1Tjj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	11250895
MGI:3715655	M	MP:0008853	decreased abdominal adipose tissue amount	Pdyn<tm1(cre)Czer>/Pdyn<tm1(cre)Czer>	involves: 129X1/SvJ * C57BL/6	N	17456788
MGI:3715655	F	MP:0003961	decreased lean body mass	Pdyn<tm1(cre)Czer>/Pdyn<tm1(cre)Czer>	involves: 129X1/SvJ * C57BL/6	N	17456788
MGI:3715655	M	MP:0001745	increased circulating corticosterone level	Pdyn<tm1(cre)Czer>/Pdyn<tm1(cre)Czer>	involves: 129X1/SvJ * C57BL/6	N	17456788
MGI:3715655	F	MP:0001402	decreased locomotor activity	Pdyn<tm1(cre)Czer>/Pdyn<tm1(cre)Czer>	involves: 129X1/SvJ * C57BL/6	N	17456788
MGI:3715655	M	MP:0008844	decreased subcutaneous adipose tissue amount	Pdyn<tm1(cre)Czer>/Pdyn<tm1(cre)Czer>	involves: 129X1/SvJ * C57BL/6	N	17456788
MGI:3715655	F	MP:0005534	decreased body temperature	Pdyn<tm1(cre)Czer>/Pdyn<tm1(cre)Czer>	involves: 129X1/SvJ * C57BL/6	N	17456788
MGI:3715655	M	MP:0010379	decreased respiratory quotient	Pdyn<tm1(cre)Czer>/Pdyn<tm1(cre)Czer>	involves: 129X1/SvJ * C57BL/6	N	17456788
MGI:3715729	F	MP:0004805	absent oocytes	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac	N	17543860
MGI:3715729	F	MP:0002777	absent ovarian follicles	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac	N	17543860
MGI:3715729	M	MP:0001147	small testis	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac	N	17543860
MGI:3715729	F	MP:0001926	female infertility	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac	N	17543860
MGI:3715729	M	MP:0008261	arrest of male meiosis	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac	N	17543860
MGI:3715729	M	MP:0013601	increased testis apoptosis	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac	N	17543860
MGI:3715729	F	MP:0005168	abnormal female meiosis	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac	N	17543860
MGI:3715729	F	MP:0001127	small ovary	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac	N	17543860
MGI:3715729	F	MP:0013507	increased ovary apoptosis	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac	N	17543860
MGI:3715729	M	MP:0001925	male infertility	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac	N	17543860
MGI:3715729	M	MP:0004901	decreased male germ cell number	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac	N	17543860
MGI:3715729	M	MP:0006379	abnormal spermatocyte morphology	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac	N	17543860
MGI:3715729	M	MP:0009451	abnormal chromosomal synapsis	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac	N	17543860
MGI:3715788	M	MP:0004852	decreased testis weight	Rb(12.Ts17<16>65Dn)2Cje/0	involves: C3H/HeSnJ * C57BL/6JEi	N	15859352
MGI:3716203	F	MP:0001386	abnormal maternal nurturing	ita/ita	involves: HRS/J * Swiss albino	N	MGI:3715281
MGI:3716203	F	MP:0001923	reduced female fertility	ita/ita	involves: HRS/J * Swiss albino	N	MGI:3715281
MGI:3716311	F	MP:0003631	nervous system phenotype	Gria3<tm1Rlh>/Gria3<tm1Rlh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	15797551
MGI:3716312	F	MP:0003631	nervous system phenotype	Gria3<tm2Rlh>/Gria3<tm2Rlh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	15797551
MGI:3716320	F	MP:0001386	abnormal maternal nurturing	Wt/Wt<+>	Not Specified	N	MGI:78277
MGI:3716320	F	MP:0001386	abnormal maternal nurturing	Wt/Wt<+>	Not Specified	N	13834122
MGI:3716330	F	MP:0005384	cellular phenotype	Xist<tm2Sado>/Xist<+>	involves: 129S1/Sv * 129X1/SvJ	Y	15992549
MGI:3716331	M	MP:0005384	cellular phenotype	Xist<tm2Sado>/Y	involves: 129S1/Sv * 129X1/SvJ	Y	15992549
MGI:3716336	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y	involves: 129S7/SvEvBrd	N	15561996
MGI:3716337	M	MP:0005389	reproductive system phenotype	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y	involves: 129S7/SvEvBrd * C57BL/6J	Y	11020714
MGI:3716338	M	MP:0000245	abnormal erythropoiesis	Gata1<tm8.2Sho>/Y	involves: 129S1/Sv	N	15895080
MGI:3716338	M	MP:0000600	liver hypoplasia	Gata1<tm8.2Sho>/Y	involves: 129S1/Sv	N	15895080
MGI:3716338	M	MP:0002417	abnormal megakaryocyte morphology	Gata1<tm8.2Sho>/Y	involves: 129S1/Sv	N	15895080
MGI:3716338	M	MP:0000603	pale liver	Gata1<tm8.2Sho>/Y	involves: 129S1/Sv	N	15895080
MGI:3716339	F	MP:0000600	liver hypoplasia	Gata1<tm8.2Sho>/Gata1<tm8.2Sho>	involves: 129S1/Sv	N	15895080
MGI:3716339	F	MP:0000245	abnormal erythropoiesis	Gata1<tm8.2Sho>/Gata1<tm8.2Sho>	involves: 129S1/Sv	N	15895080
MGI:3716339	F	MP:0002417	abnormal megakaryocyte morphology	Gata1<tm8.2Sho>/Gata1<tm8.2Sho>	involves: 129S1/Sv	N	15895080
MGI:3716339	F	MP:0000603	pale liver	Gata1<tm8.2Sho>/Gata1<tm8.2Sho>	involves: 129S1/Sv	N	15895080
MGI:3716350	M	MP:0001925	male infertility	Ocln<tm1Sts>/Ocln<tm1Sts>	involves: 129S4/SvJae * C57BL/6	N	11102513
MGI:3716350	F	MP:0001382	abnormal nursing	Ocln<tm1Sts>/Ocln<tm1Sts>	involves: 129S4/SvJae * C57BL/6	N	11102513
MGI:3716350	M	MP:0002216	abnormal seminiferous tubule morphology	Ocln<tm1Sts>/Ocln<tm1Sts>	involves: 129S4/SvJae * C57BL/6	N	11102513
MGI:3716546	F	MP:0000088	short mandible	Bmp5<cfe-se7J>/Bmp5<cfe-se7J>	involves: 129S7/SvEvBrd * BALB/cJ	N	26234751
MGI:3716546	F	MP:0000445	short snout	Bmp5<cfe-se7J>/Bmp5<cfe-se7J>	involves: 129S7/SvEvBrd * BALB/cJ	N	MGI:3716372
MGI:3716551	F	MP:0003845	abnormal decidualization	Ncoa2<tm1.1Ipc>/Ncoa2<tm1.1Ipc>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	17045797
MGI:3716551	F	MP:0000662	abnormal branching of the mammary ductal tree	Ncoa2<tm1.1Ipc>/Ncoa2<tm1.1Ipc>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	17045797
MGI:3716551	F	MP:0001926	female infertility	Ncoa2<tm1.1Ipc>/Ncoa2<tm1.1Ipc>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	17045797
MGI:3716551	F	MP:0001728	failure of embryo implantation	Ncoa2<tm1.1Ipc>/Ncoa2<tm1.1Ipc>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	17045797
MGI:3716555	F	MP:0003845	abnormal decidualization	Ncoa1<tm1Bwo>/Ncoa1<tm1Bwo>,Ncoa2<tm1.1Ipc>/Ncoa2<tm1.1Ipc>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129/Sv * 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	17045797
MGI:3716693	F	MP:0001923	reduced female fertility	Bsx<tm1Tre>/Bsx<tm1Tre>,Lep<ob>/Lep<ob>	B6.Cg-Lep<ob> Bsx<tm1Tre>	N	17550780
MGI:3716704	F	MP:0008000	increased ovary tumor incidence	Rint1<tm1Whl>/Rint1<+>	Not Specified	N	17470549
MGI:3716704	F	MP:0003570	increased uterus leiomyoma incidence	Rint1<tm1Whl>/Rint1<+>	Not Specified	N	17470549
MGI:3716806	M	MP:0005389	reproductive system phenotype	X/Sry<AKR/J>	AKR/J	Y	9383069
MGI:3716808	M	MP:0001147	small testis	Kit<W-42J>/Kit<+>,X/Sry<AKR/J>	involves: AKR/J * C57BL/6J	N	8951075
MGI:3716808	M	MP:0002213	true hermaphroditism	Kit<W-42J>/Kit<+>,X/Sry<AKR/J>	involves: AKR/J * C57BL/6J	N	8951075
MGI:3716809	M	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance	Kit<W-42J>/Kit<W-42J>,X/Sry<AKR/J>	involves: AKR/J * C57BL/6J	N	8951075
MGI:3716809	M	MP:0009205	abnormal internal male genitalia morphology	Kit<W-42J>/Kit<W-42J>,X/Sry<AKR/J>	involves: AKR/J * C57BL/6J	N	8951075
MGI:3716839	F	MP:0001382	abnormal nursing	Apoe<shl>/Apoe<shl>	KOR-Apoe<shl>	N	11866033
MGI:3716929	M	MP:0013317	abnormal seminal vesicle development	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	M	MP:0001932	abnormal spermiogenesis	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	M	MP:0002717	abnormal male preputial gland morphology	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	F	MP:0009009	absent estrous cycle	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	M	MP:0005159	azoospermia	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	F	MP:0001119	abnormal female reproductive system morphology	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	M	MP:0004852	decreased testis weight	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	F	MP:0001142	abnormal vagina orifice morphology	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	F	MP:0001132	absent mature ovarian follicles	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	F	MP:0008869	anovulation	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	F	MP:0002637	small uterus	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	M	MP:0005188	small penis	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	F	MP:0004905	decreased uterus weight	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	M	MP:0001145	abnormal male reproductive system morphology	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	M	MP:0004109	abnormal Sertoli cell development	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	F	MP:0001134	absent corpus luteum	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	F	MP:0031239	increased atretic ovarian follicle number	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	F	MP:0003572	abnormal uterus development	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	F	MP:0001127	small ovary	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3716929	M	MP:0001156	abnormal spermatogenesis	Kiss1<tm1Coll>/Kiss1<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	17563351
MGI:3717151	F	MP:0005092	decreased double-positive T cell number	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0002223	lymphoid hypoplasia	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0002722	abnormal immune system organ morphology	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0008495	decreased IgG1 level	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0008700	decreased interleukin-4 secretion	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0008193	abnormal marginal zone B cell physiology	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0008182	decreased marginal zone B cell number	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0008496	decreased IgG2a level	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0001805	decreased IgG level	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0001806	decreased IgM level	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0008076	abnormal CD4-positive T cell differentiation	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0008688	decreased interleukin-2 secretion	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0008561	decreased tumor necrosis factor secretion	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0002459	abnormal B cell physiology	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0001800	abnormal humoral immune response	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0008661	decreased interleukin-10 secretion	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0004751	increased length of allograft survival	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0008567	decreased interferon-gamma secretion	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0008133	decreased Peyer's patch number	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0005095	decreased T cell proliferation	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0004939	abnormal B cell morphology	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0001845	abnormal inflammatory response	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717151	F	MP:0008037	abnormal T cell morphology	Sash3<tm1Hlz>/Sash3<tm1Hlz>	B6.129P2-Sash3<tm1Hlz>	N	16227612
MGI:3717159	M	MP:0002675	asthenozoospermia	Spem1<tm1Wyan>/Spem1<tm1Wyan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17426145
MGI:3717159	M	MP:0001925	male infertility	Spem1<tm1Wyan>/Spem1<tm1Wyan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17426145
MGI:3717159	M	MP:0001156	abnormal spermatogenesis	Spem1<tm1Wyan>/Spem1<tm1Wyan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17426145
MGI:3717159	M	MP:0001932	abnormal spermiogenesis	Spem1<tm1Wyan>/Spem1<tm1Wyan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17426145
MGI:3717159	M	MP:0009230	abnormal sperm head morphology	Spem1<tm1Wyan>/Spem1<tm1Wyan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17426145
MGI:3717159	M	MP:0005578	teratozoospermia	Spem1<tm1Wyan>/Spem1<tm1Wyan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	17426145
MGI:3717194	F	MP:0001923	reduced female fertility	Mbtps1<wrt>/Mbtps1<wrt>	C57BL/6J-Mbtps1<wrt>	N	MGI:3717185
MGI:3717203	M	MP:0001154	seminiferous tubule degeneration	Bmp4<tm1.1Jlch>/Bmp4<tm1.1Jlch>	B6.129-Bmp4<tm1.1Jlch>	N	16624858
MGI:3717203	M	MP:0001147	small testis	Bmp4<tm1.1Jlch>/Bmp4<tm1.1Jlch>	B6.129-Bmp4<tm1.1Jlch>	N	16624858
MGI:3717244	M	MP:0004852	decreased testis weight	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717244	M	MP:0004901	decreased male germ cell number	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717244	M	MP:0001153	small seminiferous tubules	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717244	M	MP:0003642	absent seminal vesicle	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717244	M	MP:0001146	abnormal testis morphology	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717244	M	MP:0002780	decreased circulating testosterone level	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717244	M	MP:0001159	absent prostate gland	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717244	M	MP:0001145	abnormal male reproductive system morphology	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717244	M	MP:0008261	arrest of male meiosis	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717244	M	MP:0005159	azoospermia	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717244	M	MP:0002286	cryptorchism	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717244	M	MP:0001147	small testis	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717244	M	MP:0001155	arrest of spermatogenesis	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717244	M	MP:0001262	decreased body weight	Ar<tm1.1Jdz>/Y	B6.129X1-Ar<tm1.1Jdz>	N	16326839
MGI:3717247	M	MP:0002169	no abnormal phenotype detected	Ar<tm1Jdz>/Y	B6.129X1-Ar<tm1Jdz>	N	16326839
MGI:3717256	M	MP:0002780	decreased circulating testosterone level	Ar<tm1.1Jdz>/Y	involves: 129X1/SvJ * C57BL/6	N	17317769
MGI:3717256	M	MP:0001146	abnormal testis morphology	Ar<tm1.1Jdz>/Y	involves: 129X1/SvJ * C57BL/6	N	17317769
MGI:3717256	M	MP:0001159	absent prostate gland	Ar<tm1.1Jdz>/Y	involves: 129X1/SvJ * C57BL/6	N	17317769
MGI:3717256	M	MP:0005378	growth/size/body region phenotype	Ar<tm1.1Jdz>/Y	involves: 129X1/SvJ * C57BL/6	Y	17317769
MGI:3717256	M	MP:0004727	absent epididymis	Ar<tm1.1Jdz>/Y	involves: 129X1/SvJ * C57BL/6	N	17317769
MGI:3717256	M	MP:0004852	decreased testis weight	Ar<tm1.1Jdz>/Y	involves: 129X1/SvJ * C57BL/6	N	17317769
MGI:3717256	M	MP:0003642	absent seminal vesicle	Ar<tm1.1Jdz>/Y	involves: 129X1/SvJ * C57BL/6	N	17317769
MGI:3717256	M	MP:0003550	short perineum	Ar<tm1.1Jdz>/Y	involves: 129X1/SvJ * C57BL/6	N	17317769
MGI:3717256	M	MP:0002670	absent scrotum	Ar<tm1.1Jdz>/Y	involves: 129X1/SvJ * C57BL/6	N	17317769
MGI:3717256	M	MP:0002286	cryptorchism	Ar<tm1.1Jdz>/Y	involves: 129X1/SvJ * C57BL/6	N	17317769
MGI:3717269	F	MP:0004868	increased endometrial carcinoma incidence	Pten<tm1Mak>/Pten<+>	B6.129P2-Pten<tm1Mak>	N	15492213
MGI:3717274	F	MP:0004868	increased endometrial carcinoma incidence	Grb2<tm1Paw>/Grb2<+>,Pten<tm1Mak>/Pten<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	15492213
MGI:3717428	M	MP:0013899	abnormal seminal vesicle epithelium morphology	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6 * FVB/NCrl	N	17317769
MGI:3717428	M	MP:0005378	growth/size/body region phenotype	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6 * FVB/NCrl	Y	17317769
MGI:3717428	M	MP:0004929	decreased epididymis weight	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6 * FVB/NCrl	N	17317769
MGI:3717428	M	MP:0001163	abnormal prostate gland anterior lobe morphology	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6 * FVB/NCrl	N	17317769
MGI:3717428	M	MP:0000664	small prostate gland anterior lobe	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6 * FVB/NCrl	N	17317769
MGI:3717428	M	MP:0002774	small prostate gland	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6 * FVB/NCrl	N	17317769
MGI:3717428	M	MP:0001158	abnormal prostate gland morphology	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6 * FVB/NCrl	N	17317769
MGI:3717428	M	MP:0000661	small prostate gland ventral lobe	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6 * FVB/NCrl	N	17317769
MGI:3717428	M	MP:0001168	abnormal prostate gland epithelium morphology	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6 * FVB/NCrl	N	17317769
MGI:3717428	M	MP:0004910	decreased seminal vesicle weight	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6 * FVB/NCrl	N	17317769
MGI:3717428	M	MP:0004962	decreased prostate gland weight	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6 * FVB/NCrl	N	17317769
MGI:3717608	F	MP:0009021	absent estrus	Nr2f2<tm1Tsa>/Nr2f2<+>	involves: 129S7/SvEvBrd * C57BL/6	N	15890675
MGI:3717608	F	MP:0001126	abnormal ovary morphology	Nr2f2<tm1Tsa>/Nr2f2<+>	involves: 129S7/SvEvBrd * C57BL/6	N	15890675
MGI:3717608	F	MP:0001923	reduced female fertility	Nr2f2<tm1Tsa>/Nr2f2<+>	involves: 129S7/SvEvBrd * C57BL/6	N	15890675
MGI:3717608	F	MP:0009011	prolonged diestrus	Nr2f2<tm1Tsa>/Nr2f2<+>	involves: 129S7/SvEvBrd * C57BL/6	N	15890675
MGI:3717608	F	MP:0009085	abnormal uterine horn morphology	Nr2f2<tm1Tsa>/Nr2f2<+>	involves: 129S7/SvEvBrd * C57BL/6	N	15890675
MGI:3717608	F	MP:0009009	absent estrous cycle	Nr2f2<tm1Tsa>/Nr2f2<+>	involves: 129S7/SvEvBrd * C57BL/6	N	15890675
MGI:3717608	F	MP:0009020	prolonged metestrus	Nr2f2<tm1Tsa>/Nr2f2<+>	involves: 129S7/SvEvBrd * C57BL/6	N	15890675
MGI:3717637	F	MP:0004378	frontal bone foramen	Efnb1<tm1.1Sor>/Efnb1<+>	involves: 129S4/SvJaeSor * C57BL/6	N	16968134
MGI:3717637	F	MP:0003631	nervous system phenotype	Efnb1<tm1.1Sor>/Efnb1<+>	involves: 129S4/SvJaeSor * C57BL/6	Y	19515977
MGI:3717637	F	MP:0002098	abnormal vibrissa morphology	Efnb1<tm1.1Sor>/Efnb1<+>	involves: 129S4/SvJaeSor * C57BL/6	N	16968134
MGI:3717637	F	MP:0000107	abnormal frontal bone morphology	Efnb1<tm1.1Sor>/Efnb1<+>	involves: 129S4/SvJaeSor * C57BL/6	N	16968134
MGI:3717638	F	MP:0003840	abnormal coronal suture morphology	Efnb1<tm1.1Sor>/Efnb1<+>,Efnb2<tm2Sor>/Efnb2<tm2Sor>	involves: 129S4/SvJaeSor * C57BL/6	N	16968134
MGI:3717638	F	MP:0000107	abnormal frontal bone morphology	Efnb1<tm1.1Sor>/Efnb1<+>,Efnb2<tm2Sor>/Efnb2<tm2Sor>	involves: 129S4/SvJaeSor * C57BL/6	N	16968134
MGI:3717639	M	MP:0005382	craniofacial phenotype	Efnb1<tm1.1Sor>/Y,Efnb2<tm2Sor>/Efnb2<tm2Sor>	involves: 129S4/SvJaeSor * C57BL/6	Y	16968134
MGI:3717646	F	MP:0001728	failure of embryo implantation	Pcyt1a<tm1.1Irt>/Pcyt1a<tm1.1Irt>	involves: FVB/N	N	15798219
MGI:3717661	F	MP:0001984	abnormal olfaction	Cnga2<tm1Ngai>/Cnga2<tm1Ngai>	involves: 129S1/Sv * FVB/N	N	15071119
MGI:3717661	F	MP:0001983	abnormal olfactory system physiology	Cnga2<tm1Ngai>/Cnga2<tm1Ngai>	involves: 129S1/Sv * FVB/N	N	15071119
MGI:3717665	M	MP:0004512	anosmia	Cnga2<tm1Ngai>/Y	involves: 129S1/Sv	N	8893025
MGI:3717665	M	MP:0001983	abnormal olfactory system physiology	Cnga2<tm1Ngai>/Y	involves: 129S1/Sv	N	8893025
MGI:3717665	M	MP:0011085	postnatal lethality, complete penetrance	Cnga2<tm1Ngai>/Y	involves: 129S1/Sv	N	8893025
MGI:3717667	M	MP:0003631	nervous system phenotype	Cnga2<tm1Reed>/Y	involves: 129/Sv * BALB/cJ	Y	11257220
MGI:3717667	M	MP:0001983	abnormal olfactory system physiology	Cnga2<tm1Reed>/Y	involves: 129/Sv * BALB/cJ	N	11257220
MGI:3717667	M	MP:0010055	abnormal sensory neuron physiology	Cnga2<tm1Reed>/Y	involves: 129/Sv * BALB/cJ	N	11257220
MGI:3717668	F	MP:0006092	abnormal olfactory sensory neuron morphology	Cnga2<tm1Reed>/Cnga2<+>	involves: 129/Sv * BALB/cJ	N	11257220
MGI:3717728	F	MP:0004047	abnormal milk composition	Lalba<tm1Asty>/Lalba<tm1Asty>	involves: 129P2/OlaHsd	N	7708733
MGI:3717730	M	MP:0001925	male infertility	Herc2<jdf2-1R>/Herc2<jdf2-1R>	Not Specified	N	MGI:3588414
MGI:3717730	F	MP:0001926	female infertility	Herc2<jdf2-1R>/Herc2<jdf2-1R>	Not Specified	N	MGI:3588414
MGI:3717731	M	MP:0001925	male infertility	Herc2<jdf2-2R>/Herc2<jdf2-2R>	Not Specified	N	MGI:3588414
MGI:3717731	F	MP:0001926	female infertility	Herc2<jdf2-2R>/Herc2<jdf2-2R>	Not Specified	N	MGI:3588414
MGI:3717734	M	MP:0001925	male infertility	Herc2<jdf2-8R>/Herc2<jdf2-8R>	Not Specified	N	MGI:3588414
MGI:3717734	F	MP:0001926	female infertility	Herc2<jdf2-8R>/Herc2<jdf2-8R>	Not Specified	N	MGI:3588414
MGI:3717759	M	MP:0002216	abnormal seminiferous tubule morphology	Sfrp2<C50F>/Sfrp2<C50F>,Sfrp5<Q27stop>/Sfrp5<Q27stop>	involves: BALB/c * C3H/HeH	N	16700072
MGI:3717766	F	MP:0003845	abnormal decidualization	Prl8a2<tm1Soar>/Prl8a2<tm1Soar>	either: B6.129-Prl8a2<tm1Soar> or 129X1.129-Prl8a2<tm1Soar>	N	17166917
MGI:3717766	F	MP:0001126	abnormal ovary morphology	Prl8a2<tm1Soar>/Prl8a2<tm1Soar>	either: B6.129-Prl8a2<tm1Soar> or 129X1.129-Prl8a2<tm1Soar>	N	17166917
MGI:3717875	M	MP:0002060	abnormal skin morphology	Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(KRT14-rtTA)208Jek/Y,Tg(tetO-KLF4)32831Rup/0	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6NTac * SJL	N	15674344
MGI:3717902	M	MP:0001222	epidermal hyperplasia	Tg(KRT14-rtTA)208Jek/Y,Tg(tetO-KLF4)32831Rup/0	involves: C57BL/6 * SJL	N	15674344
MGI:3717902	M	MP:0001242	hyperkeratosis	Tg(KRT14-rtTA)208Jek/Y,Tg(tetO-KLF4)32831Rup/0	involves: C57BL/6 * SJL	N	15674344
MGI:3717902	M	MP:0001231	abnormal epidermis stratum basale morphology	Tg(KRT14-rtTA)208Jek/Y,Tg(tetO-KLF4)32831Rup/0	involves: C57BL/6 * SJL	N	15674344
MGI:3717902	M	MP:0000649	sebaceous gland atrophy	Tg(KRT14-rtTA)208Jek/Y,Tg(tetO-KLF4)32831Rup/0	involves: C57BL/6 * SJL	N	15674344
MGI:3717902	M	MP:0001212	skin lesions	Tg(KRT14-rtTA)208Jek/Y,Tg(tetO-KLF4)32831Rup/0	involves: C57BL/6 * SJL	N	15674344
MGI:3717902	M	MP:0003413	hair follicle degeneration	Tg(KRT14-rtTA)208Jek/Y,Tg(tetO-KLF4)32831Rup/0	involves: C57BL/6 * SJL	N	15674344
MGI:3717902	M	MP:0001510	abnormal coat appearance	Tg(KRT14-rtTA)208Jek/Y,Tg(tetO-KLF4)32831Rup/0	involves: C57BL/6 * SJL	N	15674344
MGI:3717902	M	MP:0002060	abnormal skin morphology	Tg(KRT14-rtTA)208Jek/Y,Tg(tetO-KLF4)32831Rup/0	involves: C57BL/6 * SJL	N	15674344
MGI:3717902	M	MP:0001216	abnormal epidermal layer morphology	Tg(KRT14-rtTA)208Jek/Y,Tg(tetO-KLF4)32831Rup/0	involves: C57BL/6 * SJL	N	15674344
MGI:3718113	F	MP:0001926	female infertility	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	involves: 129S2/SvPas * C57BL/6J	N	16619002
MGI:3718209	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Xist<tm3Nbd>/Xist<+>	involves: 129P2/OlaHsd * C57BL/6	N	12952890
MGI:3718210	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Xist<tm2.1Nbd>/Xist<+>	involves: 129P2/OlaHsd * C57BL/6	N	12952890
MGI:3718211	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Xist<tm2Nbd>/Xist<+>	involves: 129P2/OlaHsd * C57BL/6	N	12952890
MGI:3718212	F	MP:0005384	cellular phenotype	Xist<tm1.1Nbd>/Xist<+>	involves: 129 * C57BL/6	Y	12952890
MGI:3718214	F	MP:0005384	cellular phenotype	Rps12-ps1/Xist<tm1Nbd>/Xist<+>	involves: 129P2/OlaHsd * C57BL/6	Y	12952890
MGI:3718216	F	MP:0005384	cellular phenotype	Rps12-ps1/Xist<tm1Nbd>/Rps12-ps1<+>	involves: 129P2/OlaHsd * C57BL/6	Y	12952890
MGI:3718217	F	MP:0005384	cellular phenotype	Rps12-ps1/Xist<tm1.1Nbd>/Xist<+>	involves: 129P2/OlaHsd * C57BL/6	Y	12952890
MGI:3718218	F	MP:0005384	cellular phenotype	Rps12-ps1/Xist<tm1.1Nbd>/Rps12-ps1<+>	involves: 129P2/OlaHsd * C57BL/6	Y	12952890
MGI:3718319	M	MP:0001925	male infertility	Hoxd11<tm1Ipc>/Hoxd11<tm1Ipc>	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	7816839
MGI:3718342	M	MP:0004811	abnormal neuron physiology	Cnga2<tm1Mom>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718342	M	MP:0001983	abnormal olfactory system physiology	Cnga2<tm1Mom>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718342	M	MP:0011086	postnatal lethality, incomplete penetrance	Cnga2<tm1Mom>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718342	M	MP:0001732	postnatal growth retardation	Cnga2<tm1Mom>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718343	F	MP:0011086	postnatal lethality, incomplete penetrance	Cnga2<tm1Mom>/Cnga2<tm1Mom>	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718343	F	MP:0001983	abnormal olfactory system physiology	Cnga2<tm1Mom>/Cnga2<tm1Mom>	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718343	F	MP:0004811	abnormal neuron physiology	Cnga2<tm1Mom>/Cnga2<tm1Mom>	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718343	F	MP:0001732	postnatal growth retardation	Cnga2<tm1Mom>/Cnga2<tm1Mom>	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718345	F	MP:0004811	abnormal neuron physiology	Cnga2<tm1Mom>/Cnga2<tm1Mom>,Or8a1b<tm5(Cnga2)Mom>/Or8a1b<+>	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718345	F	MP:0001983	abnormal olfactory system physiology	Cnga2<tm1Mom>/Cnga2<tm1Mom>,Or8a1b<tm5(Cnga2)Mom>/Or8a1b<+>	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718346	M	MP:0004811	abnormal neuron physiology	Cnga2<tm1Mom>/Y,Or8a1b<tm5(Cnga2)Mom>/Or8a1b<+>	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718346	M	MP:0001983	abnormal olfactory system physiology	Cnga2<tm1Mom>/Y,Or8a1b<tm5(Cnga2)Mom>/Or8a1b<+>	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718347	F	MP:0000819	abnormal olfactory bulb morphology	Cnga2<tm1Mom>/Cnga2<tm1Mom>,Or8a1b<tm4Mom>/Or8a1b<+>	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718347	F	MP:0006092	abnormal olfactory sensory neuron morphology	Cnga2<tm1Mom>/Cnga2<tm1Mom>,Or8a1b<tm4Mom>/Or8a1b<+>	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718349	M	MP:0000819	abnormal olfactory bulb morphology	Cnga2<tm1Mom>/Y,Or8a1b<tm4Mom>/Or8a1b<+>	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718349	M	MP:0006092	abnormal olfactory sensory neuron morphology	Cnga2<tm1Mom>/Y,Or8a1b<tm4Mom>/Or8a1b<+>	involves: 129P2/OlaHsd * C57BL/6J	N	10798394
MGI:3718579	F	MP:0008670	decreased interleukin-12b secretion	Tlr7<tm1Aki>/Tlr7<tm1Aki>	B6.129P2-Tlr7<tm1Aki>	N	16461338
MGI:3718579	F	MP:0002376	abnormal dendritic cell physiology	Tlr7<tm1Aki>/Tlr7<tm1Aki>	B6.129P2-Tlr7<tm1Aki>	N	16461338
MGI:3718580	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(TRAMP)8247Ng/0	involves: C57BL/6	N	7724580
MGI:3718580	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(TRAMP)8247Ng/0	involves: C57BL/6	N	25122198
MGI:3718580	M	MP:0000659	prostate gland hyperplasia	Tg(TRAMP)8247Ng/0	involves: C57BL/6	N	7724580
MGI:3718593	F	MP:0008257	thin myometrium	Meox2<fla>/Meox2<fla>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:3717421
MGI:3718675	F	MP:0000627	abnormal mammary gland morphology	Mnt<tm1Awb>/Mnt<tm1.1Awb>,Tg(MMTV-cre)4Mam/?	involves: 129S6/SvEvTac * FVB/N	N	16740691
MGI:3718675	F	MP:0006271	abnormal involution of the mammary gland	Mnt<tm1Awb>/Mnt<tm1.1Awb>,Tg(MMTV-cre)4Mam/?	involves: 129S6/SvEvTac * FVB/N	N	16740691
MGI:3718710	M	MP:0004901	decreased male germ cell number	Creb3l4<tm1Noj>/Creb3l4<tm1Noj>	involves: 129S2/SvPas * C57BL/6	N	16999736
MGI:3718710	M	MP:0006380	abnormal spermatid morphology	Creb3l4<tm1Noj>/Creb3l4<tm1Noj>	involves: 129S2/SvPas * C57BL/6	N	16999736
MGI:3718785	F	MP:0002169	no abnormal phenotype detected	Xic<a>/Xic<c>,Xiaf1/Xiaf1<+>	involves: 129X1/SvJ * BALB/cByJ * CAST/Ei	N	12004136
MGI:3718786	F	MP:0002169	no abnormal phenotype detected	Xic<b>/Xic<c>,Xiaf3/Xiaf3<+>	involves: 129X1/SvJ * C57BL/6J * CAST/Ei * CBA/J	N	12004136
MGI:3718787	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Xic<b>/Xic<c>,Xiaf2/Xiaf2<+>	involves: 129X1/SvJ * C57BL/6J * CAST/Ei * CBA/J	N	12930754
MGI:3718794	M	MP:0001147	small testis	Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	17599069
MGI:3718794	M	MP:0001925	male infertility	Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	17599069
MGI:3718794	F	MP:0005431	decreased oocyte number	Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	17599069
MGI:3718794	F	MP:0001926	female infertility	Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	17599069
MGI:3718794	M	MP:0008261	arrest of male meiosis	Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	17599069
MGI:3718794	M	MP:0004901	decreased male germ cell number	Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	17599069
MGI:3718794	F	MP:0005168	abnormal female meiosis	Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	17599069
MGI:3718794	M	MP:0005159	azoospermia	Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	17599069
MGI:3718979	F	MP:0000628	abnormal mammary gland development	Cited1<tm1Fmar>/Cited1<tm1Fmar>	involves: 129S4/SvJae	N	16278680
MGI:3718979	F	MP:0005367	renal/urinary system phenotype	Cited1<tm1Fmar>/Cited1<tm1Fmar>	involves: 129S4/SvJae	Y	17615577
MGI:3718979	F	MP:0000662	abnormal branching of the mammary ductal tree	Cited1<tm1Fmar>/Cited1<tm1Fmar>	involves: 129S4/SvJae	N	16278680
MGI:3718981	F	MP:0011092	embryonic lethality, complete penetrance	Cited1<tm1Fmar>/Cited1<tm1Fmar>,Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	17615577
MGI:3718981	F	MP:0005367	renal/urinary system phenotype	Cited1<tm1Fmar>/Cited1<tm1Fmar>,Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	Y	17615577
MGI:3718982	F	MP:0005367	renal/urinary system phenotype	Cited1<tm1Fmar>/Cited1<tm1Fmar>,Cited2<tm1Bha>/Cited2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	Y	17615577
MGI:3719052	M	MP:0014052	increased male germ cell apoptosis	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * SJL	N	17360455
MGI:3719052	M	MP:0003205	testicular atrophy	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * SJL	N	17360455
MGI:3719089	M	MP:0003830	abnormal testis development	Sox9<tm2Crm>/Sox9<tm2Crm>,Tg(Nr5a1-cre)5Asc/?	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	15056615
MGI:3719089	M	MP:0002216	abnormal seminiferous tubule morphology	Sox9<tm2Crm>/Sox9<tm2Crm>,Tg(Nr5a1-cre)5Asc/?	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	15056615
MGI:3719089	M	MP:0005169	abnormal male meiosis	Sox9<tm2Crm>/Sox9<tm2Crm>,Tg(Nr5a1-cre)5Asc/?	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	15056615
MGI:3719099	M	MP:0011086	postnatal lethality, incomplete penetrance	Efnb1<tm1Sor>/Y,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * C57BL/6	N	15037550
MGI:3719100	F	MP:0011086	postnatal lethality, incomplete penetrance	Efnb1<tm1Sor>/Efnb1<tm1Sor>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor	N	15037550
MGI:3719101	M	MP:0011086	postnatal lethality, incomplete penetrance	Efnb1<tm1Sor>/Y,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor	N	15037550
MGI:3719102	F	MP:0011086	postnatal lethality, incomplete penetrance	Efnb1<tm1Sor>/Efnb1<+>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * C57BL/6	N	15037550
MGI:3719102	F	MP:0006322	abnormal perichondrium morphology	Efnb1<tm1Sor>/Efnb1<+>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * C57BL/6	N	15037550
MGI:3719102	F	MP:0000562	polydactyly	Efnb1<tm1Sor>/Efnb1<+>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * C57BL/6	N	15037550
MGI:3719103	F	MP:0011086	postnatal lethality, incomplete penetrance	Efnb1<tm1Sor>/Efnb1<+>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor	N	15037550
MGI:3719103	F	MP:0000562	polydactyly	Efnb1<tm1Sor>/Efnb1<+>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor	N	15037550
MGI:3719104	F	MP:0000030	abnormal tympanic ring morphology	Efnb1<tm1Sor>/Efnb1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJaeSor * C57BL/6 * CBA	N	15037550
MGI:3719104	F	MP:0000111	cleft palate	Efnb1<tm1Sor>/Efnb1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJaeSor * C57BL/6 * CBA	N	15037550
MGI:3719104	F	MP:0009886	failure of palatal shelf elevation	Efnb1<tm1Sor>/Efnb1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJaeSor * C57BL/6 * CBA	N	15037550
MGI:3719250	M	MP:0001925	male infertility	Tyrp1<b-1FCHLc>/Tyrp1<b-1FCHLc>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3719250	F	MP:0001923	reduced female fertility	Tyrp1<b-1FCHLc>/Tyrp1<b-1FCHLc>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3719285	F	MP:0001923	reduced female fertility	Tyrp1<b>/Tyrp1<b-3CHLe>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3719285	M	MP:0001922	reduced male fertility	Tyrp1<b>/Tyrp1<b-3CHLe>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3719351	F	MP:0004770	abnormal synaptic vesicle recycling	Syn1<tm1Noh>/Syn1<tm1Noh>	involves: 129S4/SvJae * C57BL/6	N	10352020
MGI:3719351	F	MP:0002945	abnormal inhibitory postsynaptic currents	Syn1<tm1Noh>/Syn1<tm1Noh>	involves: 129S4/SvJae * C57BL/6	N	10352020
MGI:3719351	F	MP:0004793	abnormal synaptic vesicle clustering	Syn1<tm1Noh>/Syn1<tm1Noh>	involves: 129S4/SvJae * C57BL/6	N	10352020
MGI:3719394	F	MP:0001926	female infertility	Kitl<Sl-3R>/Kitl<Sl-12R>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3719395	F	MP:0001926	female infertility	Kitl<Sl-12R>/Kitl<Sl-12R>	involves: 101/Rl * C3H/Rl	N	MGI:3588414
MGI:3719398	F	MP:0004996	abnormal CNS synapse formation	Syn1<tm1Noh>/Syn1<tm1Noh>	involves: 129S4/SvJae	N	8557745
MGI:3719398	F	MP:0004793	abnormal synaptic vesicle clustering	Syn1<tm1Noh>/Syn1<tm1Noh>	involves: 129S4/SvJae	N	8557745
MGI:3719399	F	MP:0004996	abnormal CNS synapse formation	Syn1<tm2Noh>/Syn1<tm2Noh>	involves: 129S4/SvJae	N	8557745
MGI:3719399	F	MP:0004793	abnormal synaptic vesicle clustering	Syn1<tm2Noh>/Syn1<tm2Noh>	involves: 129S4/SvJae	N	8557745
MGI:3719400	F	MP:0010231	transverse fur striping	Eda<Ta-4J>/Eda<+>	involves: LDJ/LeJ	N	MGI:2384532
MGI:3719479	F	MP:0004686	decreased length of long bones	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0009347	increased trabecular bone thickness	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0002998	abnormal bone remodeling	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0003419	delayed endochondral bone ossification	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0010868	increased bone trabecula number	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0005135	increased thyroid-stimulating hormone level	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0010964	increased compact bone volume	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0002932	abnormal joint morphology	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0004993	decreased bone resorption	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0006398	increased long bone epiphyseal plate size	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0004985	decreased osteoclast cell number	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0008151	increased diameter of long bones	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0001542	abnormal bone strength	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0002896	abnormal bone mineralization	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0004148	increased compact bone thickness	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0010878	increased trabecular bone volume	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0010122	abnormal bone mineral content	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0010123	increased bone mineral content	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0005474	increased triiodothyronine level	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0003953	abnormal hormone level	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0001541	abnormal osteoclast physiology	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0004214	abnormal long bone diaphysis morphology	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0000133	abnormal long bone metaphysis morphology	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719479	F	MP:0010124	decreased bone mineral content	Thra<tm1Syc>/Thra<+>	involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	N	24914936
MGI:3719575	M	MP:0001405	impaired coordination	Cdk5r1<tm1Ohsh>/Cdk5r1<tm1Ohsh>	involves: 129 * C57BL/6J	N	24802945
MGI:3719706	M	MP:0001922	reduced male fertility	Atcay<ji-hes>/Atcay<ji-hes>	C3H/HeJ-Atcay<ji-hes>	N	MGI:50295
MGI:3719842	M	MP:0001925	male infertility	T<31H>/T<+>,t<w32>/t<+>	involves: 101/H * C3H/HeH * TFH	N	10835400
MGI:3719843	M	MP:0001922	reduced male fertility	T<31H>/T<+>	involves: 101/H * C3H/HeH * TFH	N	10835400
MGI:3719845	M	MP:0001922	reduced male fertility	T<33H>/T<+>	involves: 101/H * C3H/HeH * TFH	N	10835400
MGI:3719846	M	MP:0001925	male infertility	T<30H>/T<+>,t<w32>/t<+>	involves: 101/H * C3H/HeH * TFH	N	10835400
MGI:3719847	M	MP:0001922	reduced male fertility	T<33H>/T<+>,t<w32>/t<+>	involves: 101/H * C3H/HeH * TFH	N	10835400
MGI:3719849	M	MP:0001922	reduced male fertility	T<36H>/T<+>	involves: 101/H * C3H/HeH * TFH	N	10835400
MGI:3719863	M	MP:0001925	male infertility	T<22H>/T<+>,t<w32>/t<+>	involves: 101/H * C3H/HeH * TFH	N	10835400
MGI:3719912	M	MP:0001925	male infertility	Grid2<ho-5J>/Grid2<ho-5J>	involves: C57BLKS/J	N	MGI:61633
MGI:3719915	M	MP:0001922	reduced male fertility	Grid2<ho-8J>/Grid2<ho-8J>	B10.D2/nSnJ	N	MGI:4418202
MGI:3719915	F	MP:0001923	reduced female fertility	Grid2<ho-8J>/Grid2<ho-8J>	B10.D2/nSnJ	N	MGI:4418202
MGI:3719988	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Xist<tm1Jae>/Xist<+>	involves: 129S4/SvJae	N	15668296
MGI:3719989	F	MP:0003984	embryonic growth retardation	Xist<tm2.1Jae>/Xist<+>	involves: 129	N	21852535
MGI:3719989	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Xist<tm2.1Jae>/Xist<+>	involves: 129	N	15668296
MGI:3719990	M	MP:0005389	reproductive system phenotype	Xist<tm1Jae>/Y	involves: 129S4/SvJae	Y	12356914
MGI:3719991	M	MP:0005389	reproductive system phenotype	Xist<tm2.1Jae>/Y	Not Specified	Y	12356914
MGI:3720000	F	MP:0008056	abnormal retina ganglion cell morphology	Cacna1f<nob2>/Cacna1f<nob2>	AXB6/PgnJ	N	16597347
MGI:3720000	F	MP:0008520	disorganized retina outer plexiform layer	Cacna1f<nob2>/Cacna1f<nob2>	AXB6/PgnJ	N	16597347
MGI:3720000	F	MP:0004021	abnormal rod electrophysiology	Cacna1f<nob2>/Cacna1f<nob2>	AXB6/PgnJ	N	16597347
MGI:3720000	F	MP:0006074	abnormal retina rod bipolar cell morphology	Cacna1f<nob2>/Cacna1f<nob2>	AXB6/PgnJ	N	16597347
MGI:3720000	F	MP:0003731	abnormal retina outer nuclear layer morphology	Cacna1f<nob2>/Cacna1f<nob2>	AXB6/PgnJ	N	16597347
MGI:3720000	F	MP:0004022	abnormal cone electrophysiology	Cacna1f<nob2>/Cacna1f<nob2>	AXB6/PgnJ	N	16597347
MGI:3720000	F	MP:0006068	abnormal retina horizontal cell morphology	Cacna1f<nob2>/Cacna1f<nob2>	AXB6/PgnJ	N	16597347
MGI:3720002	M	MP:0006068	abnormal retina horizontal cell morphology	Cacna1f<nob2>/Y	AXB6/PgnJ	N	16597347
MGI:3720002	M	MP:0006074	abnormal retina rod bipolar cell morphology	Cacna1f<nob2>/Y	AXB6/PgnJ	N	16597347
MGI:3720002	M	MP:0004022	abnormal cone electrophysiology	Cacna1f<nob2>/Y	AXB6/PgnJ	N	16597347
MGI:3720002	M	MP:0003731	abnormal retina outer nuclear layer morphology	Cacna1f<nob2>/Y	AXB6/PgnJ	N	16597347
MGI:3720002	M	MP:0008056	abnormal retina ganglion cell morphology	Cacna1f<nob2>/Y	AXB6/PgnJ	N	16597347
MGI:3720002	M	MP:0008520	disorganized retina outer plexiform layer	Cacna1f<nob2>/Y	AXB6/PgnJ	N	16597347
MGI:3720002	M	MP:0004021	abnormal rod electrophysiology	Cacna1f<nob2>/Y	AXB6/PgnJ	N	16597347
MGI:3720007	M	MP:0001922	reduced male fertility	Rarg<tm1Blt>/Rarg<tm1Blt>	involves: 129P2/OlaHsd * C57BL/6J	N	7631783
MGI:3720007	M	MP:0013322	squamous metaplasia of prostate gland	Rarg<tm1Blt>/Rarg<tm1Blt>	involves: 129P2/OlaHsd * C57BL/6J	N	7631783
MGI:3720007	M	MP:0013321	squamous metaplasia of seminal vesicles	Rarg<tm1Blt>/Rarg<tm1Blt>	involves: 129P2/OlaHsd * C57BL/6J	N	7631783
MGI:3720012	F	MP:0001325	abnormal retina morphology	Rpgr<Rd9>/Rpgr<+>	C57BL/6-Rpgr<Rd9>	N	11853768
MGI:3720012	F	MP:0001325	abnormal retina morphology	Rpgr<Rd9>/Rpgr<+>	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720013	F	MP:0002864	abnormal ocular fundus morphology	Rpgr<Rd9>/Rpgr<Rd9>	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720013	F	MP:0004175	telangiectasia	Rpgr<Rd9>/Rpgr<Rd9>	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720013	F	MP:0012143	decreased a-wave amplitude	Rpgr<Rd9>/Rpgr<Rd9>	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720013	F	MP:0012144	decreased b-wave amplitude	Rpgr<Rd9>/Rpgr<Rd9>	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720013	F	MP:0002792	abnormal retina vasculature morphology	Rpgr<Rd9>/Rpgr<Rd9>	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720013	F	MP:0005103	abnormal retina pigmentation	Rpgr<Rd9>/Rpgr<Rd9>	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720013	F	MP:0002864	abnormal ocular fundus morphology	Rpgr<Rd9>/Rpgr<Rd9>	C57BL/6-Rpgr<Rd9>	N	11853768
MGI:3720014	M	MP:0003728	abnormal retina photoreceptor layer morphology	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720014	M	MP:0008515	thin retina outer nuclear layer	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720014	M	MP:0004175	telangiectasia	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720014	M	MP:0005103	abnormal retina pigmentation	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720014	M	MP:0008518	retina outer nuclear layer degeneration	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720014	M	MP:0002792	abnormal retina vasculature morphology	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720014	M	MP:0002864	abnormal ocular fundus morphology	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720014	M	MP:0008456	abnormal retina rod cell outer segment morphology	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720014	M	MP:0001326	retina degeneration	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720014	M	MP:0002864	abnormal ocular fundus morphology	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	11853768
MGI:3720014	M	MP:0012143	decreased a-wave amplitude	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720014	M	MP:0004022	abnormal cone electrophysiology	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720014	M	MP:0001006	abnormal retina cone cell morphology	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720014	M	MP:0012144	decreased b-wave amplitude	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	22563472
MGI:3720014	M	MP:0008518	retina outer nuclear layer degeneration	Rpgr<Rd9>/Y	C57BL/6-Rpgr<Rd9>	N	11853768
MGI:3720062	F	MP:0004021	abnormal rod electrophysiology	Nyx<nob>/Nyx<nob>	involves: BALB/cGr	N	16597347
MGI:3720062	F	MP:0004022	abnormal cone electrophysiology	Nyx<nob>/Nyx<nob>	involves: BALB/cGr	N	16597347
MGI:3720065	M	MP:0004022	abnormal cone electrophysiology	Nyx<nob>/Y	involves: BALB/cGr	N	16597347
MGI:3720065	M	MP:0004021	abnormal rod electrophysiology	Nyx<nob>/Y	involves: BALB/cGr	N	16597347
MGI:3720093	F	MP:0001923	reduced female fertility	Abca2<tm1Nina>/Abca2<tm1Nina>	involves: 129X1/SvJ * C57BL/6	N	17488728
MGI:3720254	F	MP:0004973	increased regulatory T cell number	Foxp3<tm1Flv>/Foxp3<+>,B9d2/Tgfb1<tm1Flv>/Tgfb1<tm2Flv>,Tg(Cd4-cre)1Cwi/?	involves: 129S6/SvEvTac * C57BL/6 * DBA/2	N	17481928
MGI:3720333	F	MP:0010249	lactation failure	Bsx<tm1Aoh>/Bsx<tm1Aoh>	either: 129S4/SvJae-Bsx<tm1Aoh> or (involves: 129S4/SvJae * C57BL/6)	N	17485440
MGI:3720333	F	MP:0006270	abnormal mammary gland growth during lactation	Bsx<tm1Aoh>/Bsx<tm1Aoh>	either: 129S4/SvJae-Bsx<tm1Aoh> or (involves: 129S4/SvJae * C57BL/6)	N	17485440
MGI:3720333	F	MP:0006271	abnormal involution of the mammary gland	Bsx<tm1Aoh>/Bsx<tm1Aoh>	either: 129S4/SvJae-Bsx<tm1Aoh> or (involves: 129S4/SvJae * C57BL/6)	N	17485440
MGI:3720333	F	MP:0014126	increased mammary gland apoptosis	Bsx<tm1Aoh>/Bsx<tm1Aoh>	either: 129S4/SvJae-Bsx<tm1Aoh> or (involves: 129S4/SvJae * C57BL/6)	N	17485440
MGI:3720334	F	MP:0006271	abnormal involution of the mammary gland	Bsx<tm2Aoh>/Bsx<tm2Aoh>	either: 129S4/SvJae-Bsx<tm2Aoh> or (involves: 129S4/SvJae * C57BL/6)	N	17485440
MGI:3720334	F	MP:0014126	increased mammary gland apoptosis	Bsx<tm2Aoh>/Bsx<tm2Aoh>	either: 129S4/SvJae-Bsx<tm2Aoh> or (involves: 129S4/SvJae * C57BL/6)	N	17485440
MGI:3720334	F	MP:0010249	lactation failure	Bsx<tm2Aoh>/Bsx<tm2Aoh>	either: 129S4/SvJae-Bsx<tm2Aoh> or (involves: 129S4/SvJae * C57BL/6)	N	17485440
MGI:3720334	F	MP:0006270	abnormal mammary gland growth during lactation	Bsx<tm2Aoh>/Bsx<tm2Aoh>	either: 129S4/SvJae-Bsx<tm2Aoh> or (involves: 129S4/SvJae * C57BL/6)	N	17485440
MGI:3720594	M	MP:0001147	small testis	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17696610
MGI:3720594	F	MP:0005431	decreased oocyte number	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17696610
MGI:3720594	M	MP:0001147	small testis	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20711356
MGI:3720594	F	MP:0001126	abnormal ovary morphology	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17696610
MGI:3720594	M	MP:0008261	arrest of male meiosis	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17696610
MGI:3720594	M	MP:0020869	immotile sperm	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17696610
MGI:3720594	M	MP:0008261	arrest of male meiosis	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20711356
MGI:3720594	F	MP:0001127	small ovary	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17696610
MGI:3720594	F	MP:0002777	absent ovarian follicles	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17696610
MGI:3720594	M	MP:0002216	abnormal seminiferous tubule morphology	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20711356
MGI:3720594	F	MP:0005168	abnormal female meiosis	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20711356
MGI:3720594	F	MP:0005168	abnormal female meiosis	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17696610
MGI:3720594	F	MP:0001129	impaired ovarian folliculogenesis	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20711356
MGI:3720608	M	MP:0004931	enlarged epididymis	Tg(MMTV-Notch4)3Rnc/0	involves: FVB/N	N	1372276
MGI:3720608	M	MP:0004933	abnormal epididymis epithelium morphology	Tg(MMTV-Notch4)3Rnc/0	involves: FVB/N	N	1372276
MGI:3720608	M	MP:0001925	male infertility	Tg(MMTV-Notch4)3Rnc/0	involves: FVB/N	N	1372276
MGI:3720608	F	MP:0001885	mammary gland duct hyperplasia	Tg(MMTV-Notch4)3Rnc/0	involves: FVB/N	N	1372276
MGI:3720608	F	MP:0010249	lactation failure	Tg(MMTV-Notch4)3Rnc/0	involves: FVB/N	N	1372276
MGI:3720608	F	MP:0000628	abnormal mammary gland development	Tg(MMTV-Notch4)3Rnc/0	involves: FVB/N	N	1372276
MGI:3720608	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTV-Notch4)3Rnc/0	involves: FVB/N	N	1372276
MGI:3720608	M	MP:0002687	oligozoospermia	Tg(MMTV-Notch4)3Rnc/0	involves: FVB/N	N	1372276
MGI:3720640	F	MP:0001927	abnormal estrous cycle	Rora<sg>/Rora<sg>	involves: C57BL/6	N	1590727
MGI:3720640	F	MP:0001386	abnormal maternal nurturing	Rora<sg>/Rora<sg>	involves: C57BL/6	N	8346298
MGI:3720640	F	MP:0001923	reduced female fertility	Rora<sg>/Rora<sg>	involves: C57BL/6	N	1590727
MGI:3720640	F	MP:0003126	abnormal external female genitalia morphology	Rora<sg>/Rora<sg>	involves: C57BL/6	N	1590727
MGI:3720640	F	MP:0003699	abnormal female reproductive system physiology	Rora<sg>/Rora<sg>	involves: C57BL/6	N	1590727
MGI:3720640	F	MP:0009020	prolonged metestrus	Rora<sg>/Rora<sg>	involves: C57BL/6	N	1590727
MGI:3720640	M	MP:0002566	abnormal sexual interaction	Rora<sg>/Rora<sg>	involves: C57BL/6	N	7667406
MGI:3720640	F	MP:0009017	prolonged estrus	Rora<sg>/Rora<sg>	involves: C57BL/6	N	1590727
MGI:3720640	F	MP:0009008	delayed estrous cycle	Rora<sg>/Rora<sg>	involves: C57BL/6	N	1590727
MGI:3720640	M	MP:0002566	abnormal sexual interaction	Rora<sg>/Rora<sg>	involves: C57BL/6	N	8352721
MGI:3720649	F	MP:0014126	increased mammary gland apoptosis	Ctnna1<tm1Efu>/Ctnna1<tm1Efu>,Tg(MMTV-cre)4Mam/?	involves: 129X1/SvJ * FVB	N	14706703
MGI:3720649	F	MP:0009504	abnormal mammary gland epithelium morphology	Ctnna1<tm1Efu>/Ctnna1<tm1Efu>,Tg(MMTV-cre)4Mam/?	involves: 129X1/SvJ * FVB	N	14706703
MGI:3720649	F	MP:0010172	abnormal mammary gland epithelium physiology	Ctnna1<tm1Efu>/Ctnna1<tm1Efu>,Tg(MMTV-cre)4Mam/?	involves: 129X1/SvJ * FVB	N	14706703
MGI:3720649	F	MP:0004047	abnormal milk composition	Ctnna1<tm1Efu>/Ctnna1<tm1Efu>,Tg(MMTV-cre)4Mam/?	involves: 129X1/SvJ * FVB	N	14706703
MGI:3720651	F	MP:0009504	abnormal mammary gland epithelium morphology	Ctnna1<tm1Efu>/Ctnna1<tm1Efu>,Tg(Wap-cre)11738Mam/?	involves: 129X1/SvJ * C57BL/6 * SJL	N	14706703
MGI:3720651	F	MP:0004047	abnormal milk composition	Ctnna1<tm1Efu>/Ctnna1<tm1Efu>,Tg(Wap-cre)11738Mam/?	involves: 129X1/SvJ * C57BL/6 * SJL	N	14706703
MGI:3720651	F	MP:0014126	increased mammary gland apoptosis	Ctnna1<tm1Efu>/Ctnna1<tm1Efu>,Tg(Wap-cre)11738Mam/?	involves: 129X1/SvJ * C57BL/6 * SJL	N	14706703
MGI:3720674	M	MP:0001922	reduced male fertility	Ace<tm2Keb>/Ace<tm2Keb>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	9153279
MGI:3720715	F	MP:0005385	cardiovascular system phenotype	Hprt1<tm1(AGT)Sig>/Hprt1<tm1(AGT)Sig>,Tg(hAGT)2041Sig/?	involves: 129P2/OlaHsd * C57BL/6 * SJL/J	Y	12388794
MGI:3720717	F	MP:0002833	increased heart weight	Hprt1<tm2(AGT)Sig>/Hprt1<tm2(AGT)Sig>,Tg(hAGT)2041Sig/?	involves: 129P2/OlaHsd * C57BL/6 * SJL/J	N	12388794
MGI:3720718	M	MP:0002842	increased systemic arterial blood pressure	Hprt1<tm2(AGT)Sig>/Y,Tg(hAGT)2041Sig/?	involves: 129P2/OlaHsd * C57BL/6 * SJL/J	N	12388794
MGI:3720727	F	MP:0002842	increased systemic arterial blood pressure	Hprt1<tm2(AGT)Sig>/Hprt1<tm2(AGT)Sig>	involves: 129P2/OlaHsd * C57BL/6J	N	10625648
MGI:3720728	M	MP:0002842	increased systemic arterial blood pressure	Hprt1<tm2(AGT)Sig>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	10625648
MGI:3720777	M	MP:0001925	male infertility	Evx2<tm3Ddu>/Evx2<tm3Ddu>,Hoxd13<tm3Ddu>/Hoxd13<tm3Ddu>	involves: 129S2/SvPas * C57BL/6	N	8978698
MGI:3720780	M	MP:0001925	male infertility	Evx2<tm1Ddu>/Evx2<tm1Ddu>	involves: 129S2/SvPas * C57BL/6J	N	8978698
MGI:3720805	M	MP:0001732	postnatal growth retardation	Mtm1<tm1.2Jman>/Y,Tg(ACTA1-cre)79Jme/?	involves: 129T1/Sv * C57BL/6 * SJL	N	12391329
MGI:3720805	M	MP:0002083	premature death	Mtm1<tm1.2Jman>/Y,Tg(ACTA1-cre)79Jme/?	involves: 129T1/Sv * C57BL/6 * SJL	N	12391329
MGI:3720805	M	MP:0000751	myopathy	Mtm1<tm1.2Jman>/Y,Tg(ACTA1-cre)79Jme/?	involves: 129T1/Sv * C57BL/6 * SJL	N	12391329
MGI:3720805	M	MP:0009413	skeletal muscle fiber atrophy	Mtm1<tm1.2Jman>/Y,Tg(ACTA1-cre)79Jme/?	involves: 129T1/Sv * C57BL/6 * SJL	N	12391329
MGI:3720805	M	MP:0009404	centrally nucleated skeletal muscle fibers	Mtm1<tm1.2Jman>/Y,Tg(ACTA1-cre)79Jme/?	involves: 129T1/Sv * C57BL/6 * SJL	N	12391329
MGI:3720806	M	MP:0002169	no abnormal phenotype detected	Mtm1<tm1.2Jman>/Y,Tg(Eno2-cre)39Jme/?	involves: 129T1/Sv * C57BL/6 * SJL	N	12391329
MGI:3720867	F	MP:0001923	reduced female fertility	Plg<tm1Dco>/Plg<tm1Dco>	involves: 129S2/SvPas * C57BL/6J	N	7586361
MGI:3720887	F	MP:0008870	increased mature ovarian follicle number	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ * C57BL/6	N	9988273
MGI:3720887	F	MP:0001130	abnormal ovarian folliculogenesis	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ * C57BL/6	N	9988273
MGI:3720887	F	MP:0009083	uterus hypertrophy	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ * C57BL/6	N	9988273
MGI:3720943	M	MP:0011619	abnormal dishabituation	Bace1<tm1Pcw>/Bace1<tm1Pcw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18385378
MGI:3720943	M	MP:0003461	abnormal response to novel object	Bace1<tm1Pcw>/Bace1<tm1Pcw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18385378
MGI:3720943	M	MP:0001486	abnormal startle reflex	Bace1<tm1Pcw>/Bace1<tm1Pcw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18385378
MGI:3720943	M	MP:0009142	decreased prepulse inhibition	Bace1<tm1Pcw>/Bace1<tm1Pcw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18385378
MGI:3720943	M	MP:0009936	abnormal dendritic spine morphology	Bace1<tm1Pcw>/Bace1<tm1Pcw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18385378
MGI:3720943	M	MP:0004000	impaired passive avoidance behavior	Bace1<tm1Pcw>/Bace1<tm1Pcw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18385378
MGI:3720943	M	MP:0008428	abnormal spatial working memory	Bace1<tm1Pcw>/Bace1<tm1Pcw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18385378
MGI:3720943	M	MP:0009746	enhanced behavioral response to xenobiotic	Bace1<tm1Pcw>/Bace1<tm1Pcw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	18385378
MGI:3720971	M	MP:0001922	reduced male fertility	Clcn3<tm1Lamb>/Clcn3<tm1Lamb>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	12470859
MGI:3721373	M	MP:0001925	male infertility	Catsper4<tm1Wyan>/Catsper4<tm1Wyan>	involves: 129S7/SvEvBrd * C57BL/6J	N	17344468
MGI:3721373	M	MP:0002674	abnormal sperm motility	Catsper4<tm1Wyan>/Catsper4<tm1Wyan>	involves: 129S7/SvEvBrd * C57BL/6J	N	17344468
MGI:3721374	M	MP:0002674	abnormal sperm motility	Catsper3<tm1Wyan>/Catsper3<tm1Wyan>	involves: 129S7/SvEvBrd * C57BL/6J	N	17344468
MGI:3721374	M	MP:0001925	male infertility	Catsper3<tm1Wyan>/Catsper3<tm1Wyan>	involves: 129S7/SvEvBrd * C57BL/6J	N	17344468
MGI:3721386	M	MP:0002675	asthenozoospermia	Nsun7<Ste5Jcs1>/Nsun7<Ste5Jcs1>	involves: C3HeB/FeJ * C57BL/6	N	16024820
MGI:3721387	M	MP:0002674	abnormal sperm motility	Nsun7<Ste5Jcs1>/Nsun7<Ste5Jcs1>	involves: C57BL/6	N	17442852
MGI:3721387	M	MP:0001922	reduced male fertility	Nsun7<Ste5Jcs1>/Nsun7<Ste5Jcs1>	involves: C57BL/6	N	17442852
MGI:3721387	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Nsun7<Ste5Jcs1>/Nsun7<Ste5Jcs1>	involves: C57BL/6	N	17442852
MGI:3721387	M	MP:0009831	abnormal sperm midpiece morphology	Nsun7<Ste5Jcs1>/Nsun7<Ste5Jcs1>	involves: C57BL/6	N	17442852
MGI:3721791	M	MP:0005578	teratozoospermia	Sh1<SEG/Pas>/Sh1<SEG/Pas>	involves: C57BL/6J * SEG/Pas	N	17483418
MGI:3721875	M	MP:0005578	teratozoospermia	Sh2<SEG/Pas>/Sh2<SEG/Pas>	involves: C57BL/6J * SEG/Pas	N	17483418
MGI:3721876	M	MP:0005578	teratozoospermia	Sh3<SEG/Pas>/Sh3<SEG/Pas>	involves: C57BL/6J * SEG/Pas	N	17483418
MGI:3721877	M	MP:0005578	teratozoospermia	Sh4<SEG/Pas>/Sh4<SEG/Pas>	involves: C57BL/6J * SEG/Pas	N	17483418
MGI:3721878	M	MP:0002673	abnormal sperm number	Dss1<SEG/Pas>/Dss1<SEG/Pas>	involves: C57BL/6J * SEG/Pas	N	17483418
MGI:3721879	M	MP:0004852	decreased testis weight	Ltsw1<SEG/Pas>/Ltsw1<SEG/Pas>	involves: C57BL/6J * SEG/Pas	N	17483418
MGI:3721880	M	MP:0004852	decreased testis weight	Ltsw2<SEG/Pas>/Ltsw2<SEG/Pas>	involves: C57BL/6J * SEG/Pas	N	17483418
MGI:3721881	M	MP:0004961	increased prostate gland weight	Hpw1<SEG/Pas>/Hpw1<SEG/Pas>	involves: C57BL/6J * SEG/Pas	N	17483418
MGI:3722107	F	MP:0003699	abnormal female reproductive system physiology	Tcra-J<tm1Tgi>/Tcra-J<tm1Tgi>	B6.129-Tcra-J<tm1Tgi>	N	10639149
MGI:3722130	M	MP:0008892	abnormal sperm flagellum morphology	Gopc<tm1.1Tno>/Gopc<tm1.1Tno>	involves: 129S4/SvJae	N	17360959
MGI:3722130	M	MP:0009238	coiled sperm flagellum	Gopc<tm1.1Tno>/Gopc<tm1.1Tno>	involves: 129S4/SvJae	N	17360959
MGI:3722130	M	MP:0002686	globozoospermia	Gopc<tm1.1Tno>/Gopc<tm1.1Tno>	involves: 129S4/SvJae	N	17360959
MGI:3722133	M	MP:0009232	abnormal sperm nucleus morphology	Gopc<tm1.1Tno>/Gopc<tm1.1Tno>	involves: 129S4/SvJae * C57BL/6	N	12149515
MGI:3722133	M	MP:0008898	abnormal acrosome morphology	Gopc<tm1.1Tno>/Gopc<tm1.1Tno>	involves: 129S4/SvJae * C57BL/6	N	12149515
MGI:3722133	M	MP:0002675	asthenozoospermia	Gopc<tm1.1Tno>/Gopc<tm1.1Tno>	involves: 129S4/SvJae * C57BL/6	N	12149515
MGI:3722133	M	MP:0009231	detached acrosome	Gopc<tm1.1Tno>/Gopc<tm1.1Tno>	involves: 129S4/SvJae * C57BL/6	N	12149515
MGI:3722133	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Gopc<tm1.1Tno>/Gopc<tm1.1Tno>	involves: 129S4/SvJae * C57BL/6	N	12149515
MGI:3722133	M	MP:0002686	globozoospermia	Gopc<tm1.1Tno>/Gopc<tm1.1Tno>	involves: 129S4/SvJae * C57BL/6	N	12149515
MGI:3722133	M	MP:0001925	male infertility	Gopc<tm1.1Tno>/Gopc<tm1.1Tno>	involves: 129S4/SvJae * C57BL/6	N	12149515
MGI:3722133	M	MP:0008839	absent acrosome	Gopc<tm1.1Tno>/Gopc<tm1.1Tno>	involves: 129S4/SvJae * C57BL/6	N	12149515
MGI:3722133	M	MP:0001156	abnormal spermatogenesis	Gopc<tm1.1Tno>/Gopc<tm1.1Tno>	involves: 129S4/SvJae * C57BL/6	N	12149515
MGI:3722133	M	MP:0009238	coiled sperm flagellum	Gopc<tm1.1Tno>/Gopc<tm1.1Tno>	involves: 129S4/SvJae * C57BL/6	N	12149515
MGI:3722145	F	MP:0001386	abnormal maternal nurturing	Hoxb2<tm1Fmr>/Hoxb2<tm1Fmr>	involves: 129	N	10230789
MGI:3722148	F	MP:0001386	abnormal maternal nurturing	Hoxb2<tm1Mrc>/Hoxb2<tm1Mrc>	involves: 129S1/Sv * 129X1/SvJ	N	9012503
MGI:3722293	F	MP:0001923	reduced female fertility	Pparg<tm1Gonz>/Pparg<tm1Gonz>,Tg(MMTV-cre)1Mam/?	involves: 129X1/SvJ * FVB	N	11884400
MGI:3722293	F	MP:0006269	abnormal mammary gland growth during pregnancy	Pparg<tm1Gonz>/Pparg<tm1Gonz>,Tg(MMTV-cre)1Mam/?	involves: 129X1/SvJ * FVB	N	11884400
MGI:3722293	F	MP:0001926	female infertility	Pparg<tm1Gonz>/Pparg<tm1Gonz>,Tg(MMTV-cre)1Mam/?	involves: 129X1/SvJ * FVB	N	11884400
MGI:3722313	F	MP:0003950	abnormal plasma membrane morphology	Dmd<tm1Mok>/Dmd<tm1Mok>	involves: 129S/SvEv	N	11432672
MGI:3722314	M	MP:0000749	muscle degeneration	Dmd<tm1Mok>/Y	involves: 129S/SvEv	N	9299538
MGI:3722314	M	MP:0002279	abnormal diaphragm morphology	Dmd<tm1Mok>/Y	involves: 129S/SvEv	N	9299538
MGI:3722314	M	MP:0003950	abnormal plasma membrane morphology	Dmd<tm1Mok>/Y	involves: 129S/SvEv	N	11432672
MGI:3722620	F	MP:0011101	prenatal lethality, incomplete penetrance	Trp53<tm3.1Glo>/Trp53<tm3.1Glo>	B6.129S7-Trp53<tm3.1Glo>	N	23656786
MGI:3722620	M	MP:0002083	premature death	Trp53<tm3.1Glo>/Trp53<tm3.1Glo>	B6.129S7-Trp53<tm3.1Glo>	N	23656786
MGI:3722873	M	MP:0001157	small seminal vesicle	Gdf7<tm1Kng>/Gdf7<tm1Kng>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11356025
MGI:3722873	M	MP:0013318	abnormal branching involved in seminal vesicle morphogenesis	Gdf7<tm1Kng>/Gdf7<tm1Kng>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11356025
MGI:3722873	M	MP:0002059	abnormal seminal vesicle morphology	Gdf7<tm1Kng>/Gdf7<tm1Kng>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11356025
MGI:3722873	M	MP:0001925	male infertility	Gdf7<tm1Kng>/Gdf7<tm1Kng>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	11356025
MGI:3723121	F	MP:0001126	abnormal ovary morphology	Fts/Fts	involves: C3H * C57BL/6 * SJL	N	20969841
MGI:3723223	M	MP:0004901	decreased male germ cell number	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17652350
MGI:3723312	M	MP:0002717	abnormal male preputial gland morphology	Snca<tm1Nbm>/Snca<tm1Nbm>,Tg(Prnp-SNCA*A53T)AAub/Tg(Prnp-SNCA*A53T)AAub	involves: 129S6/SvEvTac * FVB/N	N	15585343
MGI:3723351	M	MP:0001922	reduced male fertility	Atf4<tm1Aki>/Atf4<tm1Aki>	involves: 129P2/OlaHsd	N	14561648
MGI:3723351	M	MP:0002769	abnormal vas deferens morphology	Atf4<tm1Aki>/Atf4<tm1Aki>	involves: 129P2/OlaHsd	N	14561648
MGI:3723486	M	MP:0001156	abnormal spermatogenesis	Fndc3a<sys>/Fndc3a<sys>	B6.Cg-Fndc3a<sys>	N	16904100
MGI:3723486	M	MP:0001925	male infertility	Fndc3a<sys>/Fndc3a<sys>	B6.Cg-Fndc3a<sys>	N	16904100
MGI:3723487	M	MP:0001156	abnormal spermatogenesis	Fndc3a<Gt(RRP208)Byg>/Fndc3a<sys>	involves: 129P2/OlaHsd * C3H * C57BL/6 * FVB/N	N	16904100
MGI:3723487	M	MP:0001925	male infertility	Fndc3a<Gt(RRP208)Byg>/Fndc3a<sys>	involves: 129P2/OlaHsd * C3H * C57BL/6 * FVB/N	N	16904100
MGI:3757551	F	MP:0031019	increased granulosa cell proliferation	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0009361	abnormal primordial ovarian follicle morphology	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0011129	decreased tertiary ovarian follicle number	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0009362	abnormal primary ovarian follicle morphology	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0008871	abnormal ovarian follicle number	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0009009	absent estrous cycle	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0003674	oxidative stress	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0005376	homeostasis/metabolism phenotype	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	Y	26083875
MGI:3757551	F	MP:0009006	prolonged estrous cycle	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0002678	increased follicle recruitment	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0001130	abnormal ovarian folliculogenesis	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0031020	premature ovarian failure	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0009017	prolonged estrus	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0003507	abnormal ovary physiology	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0011121	decreased primordial ovarian follicle number	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0012604	decreased glutathione level	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0013508	increased granulosa cell apoptosis	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757551	F	MP:0021106	abnormal secondary ovarian follicle morphology	Gclm<tm1Tjka>/Gclm<tm1Tjka>	B6.129-Gclm<tm1Tjka>	N	26083875
MGI:3757562	M	MP:0010504	abnormal RR interval	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0002083	premature death	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0001513	limb grasping	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0008947	increased neuron number	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0012574	decreased noradrenaline level	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0008950	ventricular tachycardia	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0004122	abnormal sinus arrhythmia	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0002843	decreased systemic arterial blood pressure	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0005665	increased circulating noradrenaline level	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0008543	atrial fibrillation	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0001629	abnormal heart rate	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0001636	irregular heartbeat	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0003137	abnormal impulse conducting system conduction	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0004565	decreased myocardial fiber size	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0002066	abnormal motor capabilities/coordination/movement	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0001262	decreased body weight	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757562	M	MP:0009732	ventricular premature beat	Tg(HDexon1)61Gpb/?	involves: C57BL/6 * CBA	N	22890713
MGI:3757643	F	MP:0008450	retina photoreceptor degeneration	Rpgr<tm1Tili>/Rpgr<tm1Tili>,Rpgrip1<tm1Tili>/Rpgrip1<tm1Tili>	involves: 129S4/SvJae * C57BL/6	N	12651948
MGI:3757668	M	MP:0002882	abnormal neuron morphology	Arhgef9<tm1.1Betz>/Y	B6.129P2-Arhgef9<tm1.1Betz>	N	17690689
MGI:3757668	M	MP:0001363	increased anxiety-related response	Arhgef9<tm1.1Betz>/Y	B6.129P2-Arhgef9<tm1.1Betz>	N	17690689
MGI:3757668	M	MP:0001475	reduced long-term depression	Arhgef9<tm1.1Betz>/Y	B6.129P2-Arhgef9<tm1.1Betz>	N	17690689
MGI:3757668	M	MP:0002797	increased thigmotaxis	Arhgef9<tm1.1Betz>/Y	B6.129P2-Arhgef9<tm1.1Betz>	N	17690689
MGI:3757668	M	MP:0001417	decreased exploration in new environment	Arhgef9<tm1.1Betz>/Y	B6.129P2-Arhgef9<tm1.1Betz>	N	17690689
MGI:3757668	M	MP:0002945	abnormal inhibitory postsynaptic currents	Arhgef9<tm1.1Betz>/Y	B6.129P2-Arhgef9<tm1.1Betz>	N	17690689
MGI:3757668	M	MP:0001463	abnormal spatial learning	Arhgef9<tm1.1Betz>/Y	B6.129P2-Arhgef9<tm1.1Betz>	N	17690689
MGI:3757668	M	MP:0003008	enhanced long-term potentiation	Arhgef9<tm1.1Betz>/Y	B6.129P2-Arhgef9<tm1.1Betz>	N	17690689
MGI:3757668	M	MP:0004859	abnormal synaptic plasticity	Arhgef9<tm1.1Betz>/Y	B6.129P2-Arhgef9<tm1.1Betz>	N	17690689
MGI:3757668	M	MP:0002912	abnormal excitatory postsynaptic potential	Arhgef9<tm1.1Betz>/Y	B6.129P2-Arhgef9<tm1.1Betz>	N	17690689
MGI:3758073	M	MP:0001922	reduced male fertility	Qki<qk-v>/Qki<qk-v>	involves: C3H/Di * DBA/2J	N	14169723
MGI:3758074	M	MP:0002182	abnormal astrocyte morphology	Plp1<jp>/Y	Not Specified	N	7365509
MGI:3758074	M	MP:0009358	environmentally induced seizures	Plp1<jp>/Y	Not Specified	N	14360249
MGI:3758074	M	MP:0000745	tremors	Plp1<jp>/Y	Not Specified	N	14360249
MGI:3758074	M	MP:0002083	premature death	Plp1<jp>/Y	Not Specified	N	14169723
MGI:3758074	M	MP:0002152	abnormal brain morphology	Plp1<jp>/Y	Not Specified	N	14169723
MGI:3758074	M	MP:0003997	tonic-clonic seizures	Plp1<jp>/Y	Not Specified	N	14169723
MGI:3758074	M	MP:0002083	premature death	Plp1<jp>/Y	Not Specified	N	14360249
MGI:3758074	M	MP:0009434	paraparesis	Plp1<jp>/Y	Not Specified	N	14169723
MGI:3758074	M	MP:0000953	abnormal oligodendrocyte morphology	Plp1<jp>/Y	Not Specified	N	7365509
MGI:3758074	M	MP:0008026	abnormal brain white matter morphology	Plp1<jp>/Y	Not Specified	N	14169723
MGI:3758074	M	MP:0003871	abnormal myelin sheath morphology	Plp1<jp>/Y	Not Specified	N	7365509
MGI:3758074	M	MP:0000755	hindlimb paralysis	Plp1<jp>/Y	Not Specified	N	14169723
MGI:3758074	M	MP:0000745	tremors	Plp1<jp>/Y	Not Specified	N	14169723
MGI:3758074	M	MP:0000920	abnormal myelination	Plp1<jp>/Y	Not Specified	N	14169723
MGI:3758089	M	MP:0001522	impaired swimming	Tg(Camk2a-DISC1)10Asaw/0	C57BL/6-Tg(Camk2a-DISC1)10Asaw	N	17675407
MGI:3758089	M	MP:0004924	abnormal behavior	Tg(Camk2a-DISC1)10Asaw/0	C57BL/6-Tg(Camk2a-DISC1)10Asaw	N	17675407
MGI:3758089	M	MP:0000807	abnormal hippocampus morphology	Tg(Camk2a-DISC1)10Asaw/0	C57BL/6-Tg(Camk2a-DISC1)10Asaw	N	17675407
MGI:3758089	M	MP:0000832	abnormal thalamus morphology	Tg(Camk2a-DISC1)10Asaw/0	C57BL/6-Tg(Camk2a-DISC1)10Asaw	N	17675407
MGI:3758089	M	MP:0009142	decreased prepulse inhibition	Tg(Camk2a-DISC1)10Asaw/0	C57BL/6-Tg(Camk2a-DISC1)10Asaw	N	17675407
MGI:3758089	M	MP:0000822	abnormal brain ventricle morphology	Tg(Camk2a-DISC1)10Asaw/0	C57BL/6-Tg(Camk2a-DISC1)10Asaw	N	17675407
MGI:3758089	M	MP:0001399	hyperactivity	Tg(Camk2a-DISC1)10Asaw/0	C57BL/6-Tg(Camk2a-DISC1)10Asaw	N	17675407
MGI:3758324	F	MP:0006271	abnormal involution of the mammary gland	Aebp1<tm1Hsro>/Aebp1<tm1Hsro>	involves: 129S4/SvJae * C57BL/6J	N	17299101
MGI:3758324	F	MP:0001382	abnormal nursing	Aebp1<tm1Hsro>/Aebp1<tm1Hsro>	involves: 129S4/SvJae * C57BL/6J	N	17299101
MGI:3758326	F	MP:0005455	increased susceptibility to weight gain	Tg(Fabp4-Aebp1)1Hsro/?	involves: FVB	N	16307171
MGI:3758326	F	MP:0002079	increased circulating insulin level	Tg(Fabp4-Aebp1)1Hsro/?	involves: FVB	N	16307171
MGI:3758326	F	MP:0002083	premature death	Tg(Fabp4-Aebp1)1Hsro/?	involves: FVB	N	16307171
MGI:3758326	F	MP:0000008	increased white adipose tissue amount	Tg(Fabp4-Aebp1)1Hsro/?	involves: FVB	N	16307171
MGI:3758326	F	MP:0001260	increased body weight	Tg(Fabp4-Aebp1)1Hsro/?	involves: FVB	N	16307171
MGI:3758326	F	MP:0001261	obese	Tg(Fabp4-Aebp1)1Hsro/?	involves: FVB	N	16307171
MGI:3758326	F	MP:0009115	abnormal fat cell morphology	Tg(Fabp4-Aebp1)1Hsro/?	involves: FVB	N	16307171
MGI:3758326	F	MP:0009763	increased susceptibility to induced morbidity/mortality	Tg(Fabp4-Aebp1)1Hsro/?	involves: FVB	N	16307171
MGI:3758326	F	MP:0005669	increased circulating leptin level	Tg(Fabp4-Aebp1)1Hsro/?	involves: FVB	N	16307171
MGI:3758326	F	MP:0005338	atherosclerotic lesions	Tg(Fabp4-Aebp1)1Hsro/?	involves: FVB	N	16307171
MGI:3758488	M	MP:0008143	abnormal dendrite morphology	Ophn1<tm2Bill>/Y	Not Specified	N	17728457
MGI:3758489	M	MP:0001463	abnormal spatial learning	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0001891	hydrocephaly	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0002061	abnormal aggression-related behavior	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0004924	abnormal behavior	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0000825	dilated lateral ventricle	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0006254	thin cerebral cortex	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0002912	abnormal excitatory postsynaptic potential	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0000827	dilated third ventricle	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0001415	increased exploration in new environment	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0002083	premature death	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0002797	increased thigmotaxis	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0003107	abnormal response to novelty	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0005238	increased brain size	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0001399	hyperactivity	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0003863	decreased aggression towards mice	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0008143	abnormal dendrite morphology	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758489	M	MP:0001364	decreased anxiety-related response	Ophn1<tm1Bill>/Y	involves: 129S2/SvPas	N	17728457
MGI:3758651	M	MP:0001156	abnormal spermatogenesis	Pgm3<mld1>/Pgm3<mld1>	C57BL/6-Pgm3<mld1>	N	17548465
MGI:3758651	M	MP:0001925	male infertility	Pgm3<mld1>/Pgm3<mld1>	C57BL/6-Pgm3<mld1>	N	17548465
MGI:3758652	M	MP:0001156	abnormal spermatogenesis	Pgm3<Gt(W037B08)Wrst>/Pgm3<mld1>	involves: 129S1/Sv * C57BL/6	N	17548465
MGI:3758652	M	MP:0001925	male infertility	Pgm3<Gt(W037B08)Wrst>/Pgm3<mld1>	involves: 129S1/Sv * C57BL/6	N	17548465
MGI:3758692	M	MP:0031391	increased locomotor activity	Dp(11Cops3-Rnf112)1Jrl/0	involves: 129S7/SvEvBrd * C57BL/6	N	14709593
MGI:3758712	M	MP:0011085	postnatal lethality, complete penetrance	Atp7a<Mo-13H>/Y	involves: 101/H * C3H/HeH	N	MGI:61018
MGI:3758716	M	MP:0002080	prenatal lethality	Atp7a<Mo-14H>/Y	Not Specified	N	8672124
MGI:3758717	M	MP:0001925	male infertility	Gusb<mps>/Gusb<mps>	B6.C-H2-K<bm1>/ByBir-Gusb<mps>/J	N	2495302
MGI:3758717	F	MP:0001882	abnormal lactation	Gusb<mps>/Gusb<mps>	B6.C-H2-K<bm1>/ByBir-Gusb<mps>/J	N	2495302
MGI:3758821	M	MP:0001211	wrinkled skin	Piga<tm1Tak>/Y,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	9207103
MGI:3758821	M	MP:0001192	scaly skin	Piga<tm1Tak>/Y,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	9207103
MGI:3758821	M	MP:0001240	abnormal epidermis stratum corneum morphology	Piga<tm1Tak>/Y,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	9207103
MGI:3758821	M	MP:0001240	abnormal epidermis stratum corneum morphology	Piga<tm1Tak>/Y,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	15304084
MGI:3758821	M	MP:0001242	hyperkeratosis	Piga<tm1Tak>/Y,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	9207103
MGI:3758821	M	MP:0001429	dehydration	Piga<tm1Tak>/Y,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	15304084
MGI:3758821	M	MP:0005332	abnormal amino acid level	Piga<tm1Tak>/Y,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	15304084
MGI:3758821	M	MP:0002796	impaired skin barrier function	Piga<tm1Tak>/Y,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	15304084
MGI:3758821	M	MP:0009608	abnormal epidermal lamellar body morphology	Piga<tm1Tak>/Y,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	15304084
MGI:3758821	M	MP:0011085	postnatal lethality, complete penetrance	Piga<tm1Tak>/Y,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	9207103
MGI:3758887	F	MP:0001923	reduced female fertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Inhba<tm1Zuk>/Inhba<tm3Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17609433
MGI:3758887	F	MP:0002681	increased corpora lutea number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Inhba<tm1Zuk>/Inhba<tm3Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17609433
MGI:3758887	F	MP:0009433	polyovular ovarian follicle	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Inhba<tm1Zuk>/Inhba<tm3Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17609433
MGI:3758888	F	MP:0001131	abnormal ovarian follicle morphology	Inhba<tm1Zuk>/Inhba<tm3Zuk>,Inhbb<tm1Jae>/Inhbb<tm1Jae>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6J	N	17609433
MGI:3758888	F	MP:0009363	abnormal tertiary ovarian follicle morphology	Inhba<tm1Zuk>/Inhba<tm3Zuk>,Inhbb<tm1Jae>/Inhbb<tm1Jae>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6J	N	17609433
MGI:3758888	F	MP:0001926	female infertility	Inhba<tm1Zuk>/Inhba<tm3Zuk>,Inhbb<tm1Jae>/Inhbb<tm1Jae>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6J	N	17609433
MGI:3758888	F	MP:0004805	absent oocytes	Inhba<tm1Zuk>/Inhba<tm3Zuk>,Inhbb<tm1Jae>/Inhbb<tm1Jae>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6J	N	17609433
MGI:3758888	F	MP:0004855	increased ovary weight	Inhba<tm1Zuk>/Inhba<tm3Zuk>,Inhbb<tm1Jae>/Inhbb<tm1Jae>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6J	N	17609433
MGI:3758888	F	MP:0009444	ovarian follicular cyst	Inhba<tm1Zuk>/Inhba<tm3Zuk>,Inhbb<tm1Jae>/Inhbb<tm1Jae>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6J	N	17609433
MGI:3758888	F	MP:0002681	increased corpora lutea number	Inhba<tm1Zuk>/Inhba<tm3Zuk>,Inhbb<tm1Jae>/Inhbb<tm1Jae>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6J	N	17609433
MGI:3758890	F	MP:0002681	increased corpora lutea number	Inhba<tm1Zuk>/Inhba<+>,Inhbb<tm1Jae>/Inhbb<tm1Jae>	involves: 129S4/SvJae * 129S7/SvEvBrd	N	17609433
MGI:3758890	F	MP:0001923	reduced female fertility	Inhba<tm1Zuk>/Inhba<+>,Inhbb<tm1Jae>/Inhbb<tm1Jae>	involves: 129S4/SvJae * 129S7/SvEvBrd	N	17609433
MGI:3758890	F	MP:0001926	female infertility	Inhba<tm1Zuk>/Inhba<+>,Inhbb<tm1Jae>/Inhbb<tm1Jae>	involves: 129S4/SvJae * 129S7/SvEvBrd	N	17609433
MGI:3758893	F	MP:0001923	reduced female fertility	Inhba<tm1Zuk>/Inhba<tm3Zuk>,Inhbb<tm1Jae>/Inhbb<tm1Jae>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6J	N	17609433
MGI:3758893	F	MP:0001926	female infertility	Inhba<tm1Zuk>/Inhba<tm3Zuk>,Inhbb<tm1Jae>/Inhbb<tm1Jae>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6J	N	17609433
MGI:3758908	F	MP:0001926	female infertility	Inhba<tm2Zuk>/Inhba<tm2Zuk>	involves: 129S7/SvEvBrd	N	10932194
MGI:3758908	F	MP:0003529	enlarged clitoris	Inhba<tm2Zuk>/Inhba<tm2Zuk>	involves: 129S7/SvEvBrd	N	10932194
MGI:3758908	M	MP:0004852	decreased testis weight	Inhba<tm2Zuk>/Inhba<tm2Zuk>	involves: 129S7/SvEvBrd	N	10932194
MGI:3758908	M	MP:0009200	enlarged external male genitalia	Inhba<tm2Zuk>/Inhba<tm2Zuk>	involves: 129S7/SvEvBrd	N	10932194
MGI:3758908	M	MP:0003599	large penis	Inhba<tm2Zuk>/Inhba<tm2Zuk>	involves: 129S7/SvEvBrd	N	10932194
MGI:3758909	M	MP:0009200	enlarged external male genitalia	Inhba<tm1Zuk>/Inhba<tm2Zuk>	involves: 129S7/SvEvBrd	N	10932194
MGI:3758909	F	MP:0001127	small ovary	Inhba<tm1Zuk>/Inhba<tm2Zuk>	involves: 129S7/SvEvBrd	N	10932194
MGI:3758909	F	MP:0031381	decreased secondary ovarian follicle number	Inhba<tm1Zuk>/Inhba<tm2Zuk>	involves: 129S7/SvEvBrd	N	10932194
MGI:3758909	M	MP:0003599	large penis	Inhba<tm1Zuk>/Inhba<tm2Zuk>	involves: 129S7/SvEvBrd	N	10932194
MGI:3758909	F	MP:0002682	decreased mature ovarian follicle number	Inhba<tm1Zuk>/Inhba<tm2Zuk>	involves: 129S7/SvEvBrd	N	10932194
MGI:3758909	F	MP:0003529	enlarged clitoris	Inhba<tm1Zuk>/Inhba<tm2Zuk>	involves: 129S7/SvEvBrd	N	10932194
MGI:3758909	M	MP:0002216	abnormal seminiferous tubule morphology	Inhba<tm1Zuk>/Inhba<tm2Zuk>	involves: 129S7/SvEvBrd	N	10932194
MGI:3758909	M	MP:0004852	decreased testis weight	Inhba<tm1Zuk>/Inhba<tm2Zuk>	involves: 129S7/SvEvBrd	N	10932194
MGI:3758926	F	MP:0001926	female infertility	Thra<tm1Ffla>/Thra<+>,Tg(Sycp1-cre)4Min/?	involves: 129/Sv * C57BL/6 * DBA/2	N	17622582
MGI:3758946	M	MP:0001147	small testis	Slc25a31<tm1Nte>/Slc25a31<tm1Nte>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17681941
MGI:3758946	M	MP:0004852	decreased testis weight	Slc25a31<tm1Nte>/Slc25a31<tm1Nte>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17681941
MGI:3758946	M	MP:0008261	arrest of male meiosis	Slc25a31<tm1Nte>/Slc25a31<tm1Nte>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17681941
MGI:3758946	M	MP:0014052	increased male germ cell apoptosis	Slc25a31<tm1Nte>/Slc25a31<tm1Nte>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17681941
MGI:3758946	M	MP:0006379	abnormal spermatocyte morphology	Slc25a31<tm1Nte>/Slc25a31<tm1Nte>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17681941
MGI:3758946	M	MP:0001925	male infertility	Slc25a31<tm1Nte>/Slc25a31<tm1Nte>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17681941
MGI:3758961	M	MP:0001463	abnormal spatial learning	Nlgn3<tm1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17823315
MGI:3758961	M	MP:0002945	abnormal inhibitory postsynaptic currents	Nlgn3<tm1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17823315
MGI:3758961	M	MP:0001360	abnormal social investigation	Nlgn3<tm1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17823315
MGI:3758962	M	MP:0002169	no abnormal phenotype detected	Nlgn3<tm2.1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17823315
MGI:3758964	F	MP:0005387	immune system phenotype	Foxp3<tm1Ayr>/Foxp3<tm1Ayr>,Foxn1<tm3(cre)Nrm>/Foxn1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	17353370
MGI:3758965	F	MP:0002145	abnormal T cell differentiation	Foxp3<tm1Ayr>/Foxp3<tm1Ayr>,Tg(Cd4-cre)1Cwi/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	17353370
MGI:3758965	F	MP:0005092	decreased double-positive T cell number	Foxp3<tm1Ayr>/Foxp3<tm1Ayr>,Tg(Cd4-cre)1Cwi/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	17353370
MGI:3758965	F	MP:0001823	thymus hypoplasia	Foxp3<tm1Ayr>/Foxp3<tm1Ayr>,Tg(Cd4-cre)1Cwi/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	17353370
MGI:3759138	M	MP:0009242	thin sperm flagellum	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	N	17517695
MGI:3759138	M	MP:0004543	abnormal sperm physiology	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	N	17517695
MGI:3759138	M	MP:0009834	abnormal sperm annulus morphology	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	N	17517695
MGI:3759138	M	MP:0001925	male infertility	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	N	17517695
MGI:3759138	M	MP:0009831	abnormal sperm midpiece morphology	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	N	17517695
MGI:3759138	M	MP:0003666	impaired sperm capacitation	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	N	17517695
MGI:3759138	M	MP:0009237	kinked sperm flagellum	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	N	17517695
MGI:3759138	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	N	17517695
MGI:3759138	M	MP:0004542	impaired acrosome reaction	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	N	17517695
MGI:3759138	M	MP:0002675	asthenozoospermia	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	N	17517695
MGI:3759138	M	MP:0009243	hairpin sperm flagellum	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	N	17517695
MGI:3759462	M	MP:0002769	abnormal vas deferens morphology	Robo2<tm1Rilm>/Robo2<tm1.1Rilm>,Tg(EIIa-cre)C5379Lmgd/?	involves: 129 * C57BL/6 * FVB/N	N	17357069
MGI:3759874	M	MP:0002075	abnormal coat/hair pigmentation	Crm/Y	TO	N	MGI:63219
MGI:3759874	M	MP:0002095	abnormal skin pigmentation	Crm/Y	TO	N	MGI:63219
MGI:3759874	M	MP:0003136	yellow coat color	Crm/Y	TO	N	MGI:63219
MGI:3759875	F	MP:0005366	variegated coat color	Crm/Crm<+>	TO	N	MGI:61991
MGI:3759875	F	MP:0002095	abnormal skin pigmentation	Crm/Crm<+>	TO	N	MGI:61991
MGI:3759875	F	MP:0005366	variegated coat color	Crm/Crm<+>	TO	N	MGI:63219
MGI:3759875	F	MP:0003136	yellow coat color	Crm/Crm<+>	TO	N	MGI:63219
MGI:3759875	F	MP:0002075	abnormal coat/hair pigmentation	Crm/Crm<+>	TO	N	MGI:63219
MGI:3759888	F	MP:0003136	yellow coat color	Crm/Crm	TO	N	MGI:63219
MGI:3759888	F	MP:0002095	abnormal skin pigmentation	Crm/Crm	TO	N	MGI:63219
MGI:3759888	F	MP:0002075	abnormal coat/hair pigmentation	Crm/Crm	TO	N	MGI:63219
MGI:3759993	M	MP:0001925	male infertility	Mapk8ip2<tm1Rjd>/Mapk8ip2<tm1Rjd>	involves: 129X1/SvJ * C57BL/6	N	17875667
MGI:3760087	M	MP:0008892	abnormal sperm flagellum morphology	Krt19<tm1Alki>/Krt19<tm1Alki>	involves: 129X1/SvJ * C57BL/6J	N	16015579
MGI:3760087	M	MP:0006380	abnormal spermatid morphology	Krt19<tm1Alki>/Krt19<tm1Alki>	involves: 129X1/SvJ * C57BL/6J	N	16015579
MGI:3760087	M	MP:0009238	coiled sperm flagellum	Krt19<tm1Alki>/Krt19<tm1Alki>	involves: 129X1/SvJ * C57BL/6J	N	16015579
MGI:3760087	M	MP:0009239	short sperm flagellum	Krt19<tm1Alki>/Krt19<tm1Alki>	involves: 129X1/SvJ * C57BL/6J	N	16015579
MGI:3760087	M	MP:0009241	thick sperm flagellum	Krt19<tm1Alki>/Krt19<tm1Alki>	involves: 129X1/SvJ * C57BL/6J	N	16015579
MGI:3760087	M	MP:0009377	ectopic manchette	Krt19<tm1Alki>/Krt19<tm1Alki>	involves: 129X1/SvJ * C57BL/6J	N	16015579
MGI:3760088	M	MP:0009377	ectopic manchette	Krt19<tm1Alki>/Krt19<+>	involves: 129X1/SvJ * C57BL/6J	N	16015579
MGI:3760088	M	MP:0009239	short sperm flagellum	Krt19<tm1Alki>/Krt19<+>	involves: 129X1/SvJ * C57BL/6J	N	16015579
MGI:3760088	M	MP:0009241	thick sperm flagellum	Krt19<tm1Alki>/Krt19<+>	involves: 129X1/SvJ * C57BL/6J	N	16015579
MGI:3760088	M	MP:0006380	abnormal spermatid morphology	Krt19<tm1Alki>/Krt19<+>	involves: 129X1/SvJ * C57BL/6J	N	16015579
MGI:3760088	M	MP:0008892	abnormal sperm flagellum morphology	Krt19<tm1Alki>/Krt19<+>	involves: 129X1/SvJ * C57BL/6J	N	16015579
MGI:3760088	M	MP:0009238	coiled sperm flagellum	Krt19<tm1Alki>/Krt19<+>	involves: 129X1/SvJ * C57BL/6J	N	16015579
MGI:3760091	F	MP:0011129	decreased tertiary ovarian follicle number	Smad3<tm1Cxd>/Smad3<tm1Cxd>	involves: 129S6/SvEvTac	N	11906909
MGI:3760091	F	MP:0011125	decreased primary ovarian follicle number	Smad3<tm1Cxd>/Smad3<tm1Cxd>	involves: 129S6/SvEvTac	N	11906909
MGI:3760091	F	MP:0011120	increased primordial ovarian follicle number	Smad3<tm1Cxd>/Smad3<tm1Cxd>	involves: 129S6/SvEvTac	N	11906909
MGI:3760091	F	MP:0001129	impaired ovarian folliculogenesis	Smad3<tm1Cxd>/Smad3<tm1Cxd>	involves: 129S6/SvEvTac	N	11906909
MGI:3760091	F	MP:0031381	decreased secondary ovarian follicle number	Smad3<tm1Cxd>/Smad3<tm1Cxd>	involves: 129S6/SvEvTac	N	11906909
MGI:3760091	F	MP:0001923	reduced female fertility	Smad3<tm1Cxd>/Smad3<tm1Cxd>	involves: 129S6/SvEvTac	N	11906909
MGI:3760114	M	MP:0001922	reduced male fertility	Magel2<tm1Stw>/Magel2<tm1Stw>	C57BL/6-Magel2<tm1Stw>	N	17893678
MGI:3760146	F	MP:0005168	abnormal female meiosis	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	N	17784788
MGI:3760146	M	MP:0001147	small testis	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	N	17784788
MGI:3760146	M	MP:0005159	azoospermia	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	N	17784788
MGI:3760146	M	MP:0001146	abnormal testis morphology	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	N	12855593
MGI:3760146	F	MP:0005431	decreased oocyte number	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	N	12855593
MGI:3760146	M	MP:0002216	abnormal seminiferous tubule morphology	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	N	12855593
MGI:3760146	M	MP:0006379	abnormal spermatocyte morphology	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	N	17784788
MGI:3760146	F	MP:0001126	abnormal ovary morphology	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	N	12855593
MGI:3760146	F	MP:0001125	abnormal oocyte morphology	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	N	17784788
MGI:3760146	M	MP:0002216	abnormal seminiferous tubule morphology	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	N	17784788
MGI:3760146	M	MP:0008261	arrest of male meiosis	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	N	17784788
MGI:3760146	M	MP:0001147	small testis	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	N	12855593
MGI:3760283	F	MP:0009338	increased splenocyte number	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0003179	thrombocytopenia	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0002376	abnormal dendritic cell physiology	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0005461	abnormal dendritic cell morphology	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0004762	increased anti-double stranded DNA antibody level	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0005095	decreased T cell proliferation	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0002619	abnormal lymphocyte morphology	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0003850	abnormal thymocyte activation	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	17878299
MGI:3760283	F	MP:0002407	abnormal double-negative T cell morphology	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	17878299
MGI:3760283	F	MP:0005018	decreased T cell number	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0005014	increased B cell number	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0008173	increased follicular B cell number	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0000218	increased leukocyte cell number	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0000220	increased monocyte cell number	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0008045	decreased NK cell number	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0000693	spleen hyperplasia	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	19805221
MGI:3760283	F	MP:0002408	abnormal double-positive T cell morphology	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac	N	17878299
MGI:3760284	F	MP:0002408	abnormal double-positive T cell morphology	Was<tm1Sbs>/Was<tm1Sbs>,Wasl<tm2Sbs>/Wasl<tm2Sbs>,Tg(Lck-cre)1Cwi/?	involves: 129S6/SvEvTac * C57BL/6	N	17878299
MGI:3760284	F	MP:0008083	decreased single-positive T cell number	Was<tm1Sbs>/Was<tm1Sbs>,Wasl<tm2Sbs>/Wasl<tm2Sbs>,Tg(Lck-cre)1Cwi/?	involves: 129S6/SvEvTac * C57BL/6	N	17878299
MGI:3760284	F	MP:0003850	abnormal thymocyte activation	Was<tm1Sbs>/Was<tm1Sbs>,Wasl<tm2Sbs>/Wasl<tm2Sbs>,Tg(Lck-cre)1Cwi/?	involves: 129S6/SvEvTac * C57BL/6	N	17878299
MGI:3760284	F	MP:0000490	abnormal crypts of Lieberkuhn morphology	Was<tm1Sbs>/Was<tm1Sbs>,Wasl<tm2Sbs>/Wasl<tm2Sbs>,Tg(Lck-cre)1Cwi/?	involves: 129S6/SvEvTac * C57BL/6	N	17878299
MGI:3760284	F	MP:0008082	increased single-positive T cell number	Was<tm1Sbs>/Was<tm1Sbs>,Wasl<tm2Sbs>/Wasl<tm2Sbs>,Tg(Lck-cre)1Cwi/?	involves: 129S6/SvEvTac * C57BL/6	N	17878299
MGI:3760284	F	MP:0004974	decreased regulatory T cell number	Was<tm1Sbs>/Was<tm1Sbs>,Wasl<tm2Sbs>/Wasl<tm2Sbs>,Tg(Lck-cre)1Cwi/?	involves: 129S6/SvEvTac * C57BL/6	N	17878299
MGI:3760284	F	MP:0002816	colitis	Was<tm1Sbs>/Was<tm1Sbs>,Wasl<tm2Sbs>/Wasl<tm2Sbs>,Tg(Lck-cre)1Cwi/?	involves: 129S6/SvEvTac * C57BL/6	N	17878299
MGI:3760284	F	MP:0002407	abnormal double-negative T cell morphology	Was<tm1Sbs>/Was<tm1Sbs>,Wasl<tm2Sbs>/Wasl<tm2Sbs>,Tg(Lck-cre)1Cwi/?	involves: 129S6/SvEvTac * C57BL/6	N	17878299
MGI:3760284	F	MP:0005018	decreased T cell number	Was<tm1Sbs>/Was<tm1Sbs>,Wasl<tm2Sbs>/Wasl<tm2Sbs>,Tg(Lck-cre)1Cwi/?	involves: 129S6/SvEvTac * C57BL/6	N	17878299
MGI:3760284	F	MP:0000715	decreased thymocyte number	Was<tm1Sbs>/Was<tm1Sbs>,Wasl<tm2Sbs>/Wasl<tm2Sbs>,Tg(Lck-cre)1Cwi/?	involves: 129S6/SvEvTac * C57BL/6	N	17878299
MGI:3760791	M	MP:0001925	male infertility	Kit<Mhdasow3>/Kit<Mhdasow3>	C3HeB/FeJ-Kit<Mhdasow3>	N	17612398
MGI:3760791	M	MP:0001156	abnormal spermatogenesis	Kit<Mhdasow3>/Kit<Mhdasow3>	C3HeB/FeJ-Kit<Mhdasow3>	N	17612398
MGI:3760844	F	MP:0001923	reduced female fertility	Slc7a7<Gt(OST41878)Lex>/Slc7a7<Gt(OST41878)Lex>	B6.129S-Slc7a7<Gt(OST41878)Lex>	N	17376816
MGI:3760844	F	MP:0001385	pup cannibalization	Slc7a7<Gt(OST41878)Lex>/Slc7a7<Gt(OST41878)Lex>	B6.129S-Slc7a7<Gt(OST41878)Lex>	N	17376816
MGI:3761115	M	MP:0005384	cellular phenotype	Siah1b<tm1Ddlb>/Y	involves: C57BL/6J	Y	12417719
MGI:3761185	F	MP:0003558	absent uterus	Lamc1<tm1Umr>/Lamc1<tm1Umr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	12015298
MGI:3761185	M	MP:0003642	absent seminal vesicle	Lamc1<tm1Umr>/Lamc1<tm1Umr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	12015298
MGI:3761185	M	MP:0002631	abnormal epididymis morphology	Lamc1<tm1Umr>/Lamc1<tm1Umr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	12015298
MGI:3761185	M	MP:0003557	absent vas deferens	Lamc1<tm1Umr>/Lamc1<tm1Umr>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	12015298
MGI:3761613	F	MP:0001790	abnormal immune system physiology	Fas<lpr>/Fas<lpr>,Sh2d1a<rpl>/Sh2d1a<rpl>	MRL/Mp-Fas<lpr> Sh2d1a<rpl>	N	16365433
MGI:3761613	F	MP:0004794	increased anti-nuclear antigen antibody level	Fas<lpr>/Fas<lpr>,Sh2d1a<rpl>/Sh2d1a<rpl>	MRL/Mp-Fas<lpr> Sh2d1a<rpl>	N	16365433
MGI:3761927	M	MP:0001168	abnormal prostate gland epithelium morphology	Pten<tm1Mro>/Pten<+>,Tg(KLK3-cre)D4Trp/0	involves: 129P2/OlaHsd * FVB	N	15994948
MGI:3761927	M	MP:0000659	prostate gland hyperplasia	Pten<tm1Mro>/Pten<+>,Tg(KLK3-cre)D4Trp/0	involves: 129P2/OlaHsd * FVB	N	15994948
MGI:3761927	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Mro>/Pten<+>,Tg(KLK3-cre)D4Trp/0	involves: 129P2/OlaHsd * FVB	N	15994948
MGI:3761927	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Mro>/Pten<+>,Tg(KLK3-cre)D4Trp/0	involves: 129P2/OlaHsd * FVB	N	15994948
MGI:3761927	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm1Mro>/Pten<+>,Tg(KLK3-cre)D4Trp/0	involves: 129P2/OlaHsd * FVB	N	15994948
MGI:3761927	M	MP:0004961	increased prostate gland weight	Pten<tm1Mro>/Pten<+>,Tg(KLK3-cre)D4Trp/0	involves: 129P2/OlaHsd * FVB	N	15994948
MGI:3761928	M	MP:0001167	prostate gland epithelial hyperplasia	Pten<tm1Mro>/Pten<tm1Mro>,Tg(KLK3-cre)D4Trp/0	involves: 129P2/OlaHsd * FVB	N	15994948
MGI:3762380	F	MP:0001923	reduced female fertility	Rspo2<tm1Nuv>/Rspo2<+>	involves: 129 * C57BL/6	N	17904116
MGI:3762585	F	MP:0030166	increased inner canthal distance	Limk2<whe>/Limk2<whe>	B6.Cg-Lep<ob> Limk2<whe>/GrsrJ	N	26234751
MGI:3762591	M	MP:0009232	abnormal sperm nucleus morphology	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762591	M	MP:0008892	abnormal sperm flagellum morphology	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762591	M	MP:0008898	abnormal acrosome morphology	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762591	M	MP:0008839	absent acrosome	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762591	M	MP:0002675	asthenozoospermia	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762591	M	MP:0001925	male infertility	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762591	M	MP:0005578	teratozoospermia	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762591	M	MP:0002686	globozoospermia	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762591	M	MP:0009238	coiled sperm flagellum	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762591	M	MP:0002784	abnormal Sertoli cell morphology	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762591	M	MP:0008893	detached sperm flagellum	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762591	M	MP:0001156	abnormal spermatogenesis	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762591	M	MP:0006380	abnormal spermatid morphology	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762592	M	MP:0005578	teratozoospermia	Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762592	M	MP:0001922	reduced male fertility	Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762593	M	MP:0005578	teratozoospermia	Zpbp<tm1Zuk>/Zpbp<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762594	M	MP:0002784	abnormal Sertoli cell morphology	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762594	M	MP:0009232	abnormal sperm nucleus morphology	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762594	M	MP:0006380	abnormal spermatid morphology	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762594	M	MP:0002686	globozoospermia	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762594	M	MP:0005578	teratozoospermia	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762594	M	MP:0008893	detached sperm flagellum	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762594	M	MP:0001925	male infertility	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762594	M	MP:0008892	abnormal sperm flagellum morphology	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762594	M	MP:0008898	abnormal acrosome morphology	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762594	M	MP:0002675	asthenozoospermia	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762594	M	MP:0008839	absent acrosome	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762594	M	MP:0001156	abnormal spermatogenesis	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762594	M	MP:0009238	coiled sperm flagellum	Zpbp<tm1Zuk>/Zpbp<tm1Zuk>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762595	M	MP:0001922	reduced male fertility	Zpbp<tm1Zuk>/Zpbp<+>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762595	M	MP:0005578	teratozoospermia	Zpbp<tm1Zuk>/Zpbp<+>,Zpbp2<tm1Zuk>/Zpbp2<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762596	M	MP:0001922	reduced male fertility	Zpbp<tm1Zuk>/Zpbp<+>,Zpbp2<tm1Zuk>/Zpbp2<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762596	M	MP:0005578	teratozoospermia	Zpbp<tm1Zuk>/Zpbp<+>,Zpbp2<tm1Zuk>/Zpbp2<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	17664285
MGI:3762619	M	MP:0001378	abnormal ejaculation	Grn<tm1Mni>/Grn<tm1Mni>	involves: 129P2/OlaHsd * C57BL/6J	N	17764761
MGI:3762659	M	MP:0001925	male infertility	Zbtb16<lu-Sfd>/Zbtb16<lu-Sfd>	involves: C57BL/6 * Swiss	N	6067640
MGI:3762660	M	MP:0001925	male infertility	Zbtb16<lu-Sfd>/Zbtb16<lu-Sfd>	involves: C57BL/6	N	6067640
MGI:3762762	M	MP:0006380	abnormal spermatid morphology	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	M	MP:0005148	seminal vesicle hypoplasia	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	F	MP:0002777	absent ovarian follicles	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	F	MP:0001140	abnormal vagina epithelium morphology	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	F	MP:0004856	decreased ovary weight	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	M	MP:0004852	decreased testis weight	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	M	MP:0002716	small male preputial gland	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	M	MP:0005536	decreased Leydig cell number	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	F	MP:0001926	female infertility	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	M	MP:0001145	abnormal male reproductive system morphology	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	F	MP:0002016	ovary cyst	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	M	MP:0001925	male infertility	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	F	MP:0009009	absent estrous cycle	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	F	MP:0001119	abnormal female reproductive system morphology	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762762	F	MP:0001134	absent corpus luteum	Kiss1<tm1Rla>/Kiss1<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762763	M	MP:0002716	small male preputial gland	Kiss1r<tm1Rla>/Kiss1r<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762763	M	MP:0005148	seminal vesicle hypoplasia	Kiss1r<tm1Rla>/Kiss1r<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762763	F	MP:0009009	absent estrous cycle	Kiss1r<tm1Rla>/Kiss1r<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762763	M	MP:0006380	abnormal spermatid morphology	Kiss1r<tm1Rla>/Kiss1r<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762763	M	MP:0001925	male infertility	Kiss1r<tm1Rla>/Kiss1r<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762763	M	MP:0001145	abnormal male reproductive system morphology	Kiss1r<tm1Rla>/Kiss1r<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762763	M	MP:0005536	decreased Leydig cell number	Kiss1r<tm1Rla>/Kiss1r<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762763	M	MP:0004852	decreased testis weight	Kiss1r<tm1Rla>/Kiss1r<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762763	F	MP:0004856	decreased ovary weight	Kiss1r<tm1Rla>/Kiss1r<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762763	F	MP:0001926	female infertility	Kiss1r<tm1Rla>/Kiss1r<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762763	F	MP:0001119	abnormal female reproductive system morphology	Kiss1r<tm1Rla>/Kiss1r<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762763	F	MP:0002777	absent ovarian follicles	Kiss1r<tm1Rla>/Kiss1r<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762763	F	MP:0001134	absent corpus luteum	Kiss1r<tm1Rla>/Kiss1r<tm1Rla>	involves: 129S1/SvImJ	N	17595229
MGI:3762769	M	MP:0001922	reduced male fertility	Fk/Fk<+>	involves: CBA	N	5749972
MGI:3762769	F	MP:0001923	reduced female fertility	Fk/Fk<+>	involves: CBA	N	5749972
MGI:3763086	M	MP:0004928	increased epididymis weight	Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/0	involves: FVB	N	21333348
MGI:3763086	M	MP:0004909	increased seminal vesicle weight	Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/0	involves: FVB	N	21333348
MGI:3763086	M	MP:0030603	increased sperm number	Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/0	involves: FVB	N	21333348
MGI:3763087	M	MP:0004909	increased seminal vesicle weight	Ptprv<tm1Asmi>/Ptprv<tm1Asmi>	involves: 129P2/OlaHsd	N	21333348
MGI:3763087	M	MP:0001152	increased Leydig cell number	Ptprv<tm1Asmi>/Ptprv<tm1Asmi>	involves: 129P2/OlaHsd	N	21333348
MGI:3763087	M	MP:0001148	enlarged testis	Ptprv<tm1Asmi>/Ptprv<tm1Asmi>	involves: 129P2/OlaHsd	N	21333348
MGI:3763087	M	MP:0030603	increased sperm number	Ptprv<tm1Asmi>/Ptprv<tm1Asmi>	involves: 129P2/OlaHsd	N	21333348
MGI:3763087	M	MP:0004851	increased testis weight	Ptprv<tm1Asmi>/Ptprv<tm1Asmi>	involves: 129P2/OlaHsd	N	21333348
MGI:3763087	M	MP:0004928	increased epididymis weight	Ptprv<tm1Asmi>/Ptprv<tm1Asmi>	involves: 129P2/OlaHsd	N	21333348
MGI:3763087	M	MP:0008280	abnormal male germ cell apoptosis	Ptprv<tm1Asmi>/Ptprv<tm1Asmi>	involves: 129P2/OlaHsd	N	21333348
MGI:3763089	M	MP:0002687	oligozoospermia	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763089	M	MP:0005536	decreased Leydig cell number	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763089	M	MP:0004852	decreased testis weight	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763089	M	MP:0006379	abnormal spermatocyte morphology	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763089	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763089	M	MP:0004929	decreased epididymis weight	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763089	M	MP:0004910	decreased seminal vesicle weight	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763089	M	MP:0006380	abnormal spermatid morphology	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763089	M	MP:0001147	small testis	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763090	M	MP:0004910	decreased seminal vesicle weight	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763090	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763090	M	MP:0001147	small testis	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763090	M	MP:0004852	decreased testis weight	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763090	M	MP:0006380	abnormal spermatid morphology	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763090	M	MP:0006379	abnormal spermatocyte morphology	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763090	M	MP:0002687	oligozoospermia	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763090	M	MP:0004929	decreased epididymis weight	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763090	M	MP:0005536	decreased Leydig cell number	Bglap/Bglap2<tm1Kry>/Bglap/Bglap2<tm1Kry>	involves: 129S7/SvEvBrd	N	21333348
MGI:3763181	F	MP:0001129	impaired ovarian folliculogenesis	Gja1<tm7(Gja2)Kwi>/Gja1<tm7(Gja2)Kwi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17408477
MGI:3763181	F	MP:0001134	absent corpus luteum	Gja1<tm7(Gja2)Kwi>/Gja1<tm7(Gja2)Kwi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17408477
MGI:3763181	F	MP:0002016	ovary cyst	Gja1<tm7(Gja2)Kwi>/Gja1<tm7(Gja2)Kwi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17408477
MGI:3763181	M	MP:0004852	decreased testis weight	Gja1<tm7(Gja2)Kwi>/Gja1<tm7(Gja2)Kwi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17408477
MGI:3763181	M	MP:0001925	male infertility	Gja1<tm7(Gja2)Kwi>/Gja1<tm7(Gja2)Kwi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17408477
MGI:3763181	M	MP:0001156	abnormal spermatogenesis	Gja1<tm7(Gja2)Kwi>/Gja1<tm7(Gja2)Kwi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17408477
MGI:3763181	F	MP:0001926	female infertility	Gja1<tm7(Gja2)Kwi>/Gja1<tm7(Gja2)Kwi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17408477
MGI:3763181	M	MP:0006379	abnormal spermatocyte morphology	Gja1<tm7(Gja2)Kwi>/Gja1<tm7(Gja2)Kwi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17408477
MGI:3763181	M	MP:0005159	azoospermia	Gja1<tm7(Gja2)Kwi>/Gja1<tm7(Gja2)Kwi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17408477
MGI:3763181	F	MP:0001127	small ovary	Gja1<tm7(Gja2)Kwi>/Gja1<tm7(Gja2)Kwi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17408477
MGI:3763181	F	MP:0008871	abnormal ovarian follicle number	Gja1<tm7(Gja2)Kwi>/Gja1<tm7(Gja2)Kwi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17408477
MGI:3763182	F	MP:0006269	abnormal mammary gland growth during pregnancy	Gja1<tm7(Gja2)Kwi>/Gja1<+>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17408477
MGI:3764468	F	MP:0001541	abnormal osteoclast physiology	Ctsk<tm1(cre)Ska>/Ctsk<+>,Esr1<tm1Mma>/Esr1<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	17803905
MGI:3764468	F	MP:0020010	decreased bone mineral density of femur	Ctsk<tm1(cre)Ska>/Ctsk<+>,Esr1<tm1Mma>/Esr1<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	17803905
MGI:3764468	F	MP:0020080	increased bone mineralization	Ctsk<tm1(cre)Ska>/Ctsk<+>,Esr1<tm1Mma>/Esr1<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	17803905
MGI:3764468	F	MP:0004992	increased bone resorption	Ctsk<tm1(cre)Ska>/Ctsk<+>,Esr1<tm1Mma>/Esr1<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	17803905
MGI:3764468	F	MP:0000066	osteoporosis	Ctsk<tm1(cre)Ska>/Ctsk<+>,Esr1<tm1Mma>/Esr1<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	17803905
MGI:3764468	F	MP:0020039	increased bone ossification	Ctsk<tm1(cre)Ska>/Ctsk<+>,Esr1<tm1Mma>/Esr1<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	17803905
MGI:3764468	F	MP:0004984	increased osteoclast cell number	Ctsk<tm1(cre)Ska>/Ctsk<+>,Esr1<tm1Mma>/Esr1<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	17803905
MGI:3764489	M	MP:0008151	increased diameter of long bones	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0004686	decreased length of long bones	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0000592	short tail	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0000195	decreased circulating calcium level	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0006397	disorganized long bone epiphyseal plate	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0020137	decreased bone mineralization	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	11159866
MGI:3764489	M	MP:0003109	short femur	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0014322	short hindlimb	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0011967	increased or absent threshold for auditory brainstem response	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0009445	osteomalacia	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	14751570
MGI:3764489	M	MP:0000063	decreased bone mineral density	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0002764	short tibia	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0002765	short fibula	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0001666	abnormal intestinal absorption	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	3145795
MGI:3764489	M	MP:0002759	abnormal caudal vertebrae morphology	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	14751570
MGI:3764489	M	MP:0001262	decreased body weight	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0005353	abnormal patella morphology	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0005628	decreased circulating potassium level	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764489	M	MP:0004652	small caudal vertebrae	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	14751570
MGI:3764489	M	MP:0000198	decreased circulating phosphate level	Phex<Hyp>/Y	B6.Cg-Phex<Hyp>/J	N	14751570
MGI:3764685	F	MP:0014322	short hindlimb	Phex<Hyp>/Phex<+>	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764685	F	MP:0002759	abnormal caudal vertebrae morphology	Phex<Hyp>/Phex<+>	B6.Cg-Phex<Hyp>/J	N	14751570
MGI:3764685	F	MP:0001666	abnormal intestinal absorption	Phex<Hyp>/Phex<+>	B6.Cg-Phex<Hyp>/J	N	3145795
MGI:3764685	F	MP:0002089	abnormal postnatal growth/weight/body size	Phex<Hyp>/Phex<+>	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764685	F	MP:0009445	osteomalacia	Phex<Hyp>/Phex<+>	B6.Cg-Phex<Hyp>/J	N	14751570
MGI:3764685	F	MP:0000592	short tail	Phex<Hyp>/Phex<+>	B6.Cg-Phex<Hyp>/J	N	15029877
MGI:3764685	F	MP:0000198	decreased circulating phosphate level	Phex<Hyp>/Phex<+>	B6.Cg-Phex<Hyp>/J	N	14751570
MGI:3764685	F	MP:0004652	small caudal vertebrae	Phex<Hyp>/Phex<+>	B6.Cg-Phex<Hyp>/J	N	14751570
MGI:3764685	F	MP:0005384	cellular phenotype	Phex<Hyp>/Phex<+>	B6.Cg-Phex<Hyp>/J	Y	14751570
MGI:3764912	M	MP:0002687	oligozoospermia	Kdm3a<Gt(YHA186)Byg>/Kdm3a<Gt(YHA186)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17943087
MGI:3764912	M	MP:0009230	abnormal sperm head morphology	Kdm3a<Gt(YHA186)Byg>/Kdm3a<Gt(YHA186)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17943087
MGI:3764912	M	MP:0001925	male infertility	Kdm3a<Gt(YHA186)Byg>/Kdm3a<Gt(YHA186)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17943087
MGI:3764912	M	MP:0001147	small testis	Kdm3a<Gt(YHA186)Byg>/Kdm3a<Gt(YHA186)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17943087
MGI:3764912	M	MP:0001932	abnormal spermiogenesis	Kdm3a<Gt(YHA186)Byg>/Kdm3a<Gt(YHA186)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17943087
MGI:3764912	M	MP:0002675	asthenozoospermia	Kdm3a<Gt(YHA186)Byg>/Kdm3a<Gt(YHA186)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17943087
MGI:3764912	M	MP:0001156	abnormal spermatogenesis	Kdm3a<Gt(YHA186)Byg>/Kdm3a<Gt(YHA186)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17943087
MGI:3764912	M	MP:0006380	abnormal spermatid morphology	Kdm3a<Gt(YHA186)Byg>/Kdm3a<Gt(YHA186)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17943087
MGI:3764912	M	MP:0031354	abnormal acrosome assembly	Kdm3a<Gt(YHA186)Byg>/Kdm3a<Gt(YHA186)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17943087
MGI:3764912	M	MP:0002216	abnormal seminiferous tubule morphology	Kdm3a<Gt(YHA186)Byg>/Kdm3a<Gt(YHA186)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17943087
MGI:3764917	F	MP:0012106	impaired exercise endurance	Bex1<Gt(OST125186)Lex>/Bex1<Gt(OST125186)Lex>	involves: 129S5/SvEvBrd	N	17884015
MGI:3764917	F	MP:0013237	abnormal skeletal muscle regeneration	Bex1<Gt(OST125186)Lex>/Bex1<Gt(OST125186)Lex>	involves: 129S5/SvEvBrd	N	17884015
MGI:3764932	M	MP:0004901	decreased male germ cell number	Cyp26b1<tm1.1Ptk>/Cyp26b1<tm1.1Ptk>	involves: 129S2/SvPas	N	17584971
MGI:3764932	M	MP:0008280	abnormal male germ cell apoptosis	Cyp26b1<tm1.1Ptk>/Cyp26b1<tm1.1Ptk>	involves: 129S2/SvPas	N	17584971
MGI:3764932	M	MP:0001147	small testis	Cyp26b1<tm1.1Ptk>/Cyp26b1<tm1.1Ptk>	involves: 129S2/SvPas	N	17584971
MGI:3764970	M	MP:0005188	small penis	Kiss1r<Gt1Stei>/Kiss1r<Gt1Stei>	involves: 129S1/SvImJ * C57BL/6	N	17699664
MGI:3764970	M	MP:0002566	abnormal sexual interaction	Kiss1r<Gt1Stei>/Kiss1r<Gt1Stei>	involves: 129S1/SvImJ * C57BL/6	N	17699664
MGI:3764970	M	MP:0001147	small testis	Kiss1r<Gt1Stei>/Kiss1r<Gt1Stei>	involves: 129S1/SvImJ * C57BL/6	N	17978050
MGI:3764970	F	MP:0004856	decreased ovary weight	Kiss1r<Gt1Stei>/Kiss1r<Gt1Stei>	involves: 129S1/SvImJ * C57BL/6	N	17699664
MGI:3764970	M	MP:0004852	decreased testis weight	Kiss1r<Gt1Stei>/Kiss1r<Gt1Stei>	involves: 129S1/SvImJ * C57BL/6	N	17699664
MGI:3764970	M	MP:0009856	failure of ejaculation	Kiss1r<Gt1Stei>/Kiss1r<Gt1Stei>	involves: 129S1/SvImJ * C57BL/6	N	17699664
MGI:3764970	F	MP:0001127	small ovary	Kiss1r<Gt1Stei>/Kiss1r<Gt1Stei>	involves: 129S1/SvImJ * C57BL/6	N	17978050
MGI:3764970	M	MP:0004910	decreased seminal vesicle weight	Kiss1r<Gt1Stei>/Kiss1r<Gt1Stei>	involves: 129S1/SvImJ * C57BL/6	N	17699664
MGI:3765072	F	MP:0004894	uterus atrophy	Cyp7b1<tm1Lth>/Cyp7b1<tm1Lth>	involves: 129P2/OlaHsd * C57BL/6	N	15710898
MGI:3765072	F	MP:0003572	abnormal uterus development	Cyp7b1<tm1Lth>/Cyp7b1<tm1Lth>	involves: 129P2/OlaHsd * C57BL/6	N	15710898
MGI:3765072	F	MP:0001927	abnormal estrous cycle	Cyp7b1<tm1Lth>/Cyp7b1<tm1Lth>	involves: 129P2/OlaHsd * C57BL/6	N	15710898
MGI:3765072	F	MP:0009009	absent estrous cycle	Cyp7b1<tm1Lth>/Cyp7b1<tm1Lth>	involves: 129P2/OlaHsd * C57BL/6	N	15710898
MGI:3765072	F	MP:0031020	premature ovarian failure	Cyp7b1<tm1Lth>/Cyp7b1<tm1Lth>	involves: 129P2/OlaHsd * C57BL/6	N	15710898
MGI:3765072	F	MP:0000628	abnormal mammary gland development	Cyp7b1<tm1Lth>/Cyp7b1<tm1Lth>	involves: 129P2/OlaHsd * C57BL/6	N	15710898
MGI:3765072	F	MP:0003378	early sexual maturation	Cyp7b1<tm1Lth>/Cyp7b1<tm1Lth>	involves: 129P2/OlaHsd * C57BL/6	N	15710898
MGI:3765430	F	MP:0004256	abnormal maternal decidual layer morphology	Egfr<tm1Wag>/Egfr<tm1Wag>	involves: 129 * C57BL/6	N	7618085
MGI:3765974	M	MP:0005578	teratozoospermia	Brdt<tm1Djw>/Brdt<tm1Djw>	involves: 129S/SvEv * C57BL/6J	N	17728347
MGI:3765974	M	MP:0031354	abnormal acrosome assembly	Brdt<tm1Djw>/Brdt<tm1Djw>	involves: 129S/SvEv * C57BL/6J	N	17728347
MGI:3765974	M	MP:0006380	abnormal spermatid morphology	Brdt<tm1Djw>/Brdt<tm1Djw>	involves: 129S/SvEv * C57BL/6J	N	17728347
MGI:3765974	M	MP:0009230	abnormal sperm head morphology	Brdt<tm1Djw>/Brdt<tm1Djw>	involves: 129S/SvEv * C57BL/6J	N	17728347
MGI:3765974	M	MP:0008892	abnormal sperm flagellum morphology	Brdt<tm1Djw>/Brdt<tm1Djw>	involves: 129S/SvEv * C57BL/6J	N	17728347
MGI:3765974	M	MP:0002675	asthenozoospermia	Brdt<tm1Djw>/Brdt<tm1Djw>	involves: 129S/SvEv * C57BL/6J	N	17728347
MGI:3765974	M	MP:0009831	abnormal sperm midpiece morphology	Brdt<tm1Djw>/Brdt<tm1Djw>	involves: 129S/SvEv * C57BL/6J	N	17728347
MGI:3765974	M	MP:0001925	male infertility	Brdt<tm1Djw>/Brdt<tm1Djw>	involves: 129S/SvEv * C57BL/6J	N	17728347
MGI:3765974	F	MP:0005389	reproductive system phenotype	Brdt<tm1Djw>/Brdt<tm1Djw>	involves: 129S/SvEv * C57BL/6J	Y	17728347
MGI:3765974	M	MP:0002687	oligozoospermia	Brdt<tm1Djw>/Brdt<tm1Djw>	involves: 129S/SvEv * C57BL/6J	N	17728347
MGI:3766011	M	MP:0001932	abnormal spermiogenesis	Rara<tm1Ipc>/Rara<tm1Ipc>	involves: 129S2/SvPas * C57BL/6	N	15901285
MGI:3766011	M	MP:0008280	abnormal male germ cell apoptosis	Rara<tm1Ipc>/Rara<tm1Ipc>	involves: 129S2/SvPas * C57BL/6	N	15901285
MGI:3766011	M	MP:0005578	teratozoospermia	Rara<tm1Ipc>/Rara<tm1Ipc>	involves: 129S2/SvPas * C57BL/6	N	15901285
MGI:3766011	M	MP:0001925	male infertility	Rara<tm1Ipc>/Rara<tm1Ipc>	involves: 129S2/SvPas * C57BL/6	N	15901285
MGI:3766011	M	MP:0006380	abnormal spermatid morphology	Rara<tm1Ipc>/Rara<tm1Ipc>	involves: 129S2/SvPas * C57BL/6	N	15901285
MGI:3766011	M	MP:0002687	oligozoospermia	Rara<tm1Ipc>/Rara<tm1Ipc>	involves: 129S2/SvPas * C57BL/6	N	15901285
MGI:3766018	F	MP:0009072	absent cranial vagina	Rara<tm1Ipc>/Rara<tm1Ipc>,Rarb<tm1Mma>/Rarb<tm1Mma>	involves: 129S2/SvPas * C57BL/6	N	9240560
MGI:3766018	F	MP:0003558	absent uterus	Rara<tm1Ipc>/Rara<tm1Ipc>,Rarb<tm1Mma>/Rarb<tm1Mma>	involves: 129S2/SvPas * C57BL/6	N	9240560
MGI:3766018	F	MP:0003575	absent oviduct	Rara<tm1Ipc>/Rara<tm1Ipc>,Rarb<tm1Mma>/Rarb<tm1Mma>	involves: 129S2/SvPas * C57BL/6	N	9240560
MGI:3766097	F	MP:0001510	abnormal coat appearance	Bhrd/Bhrd<+>	B6(V)-Bhrd/GrsrJ	N	MGI:3765079
MGI:3766097	F	MP:0000418	focal hair loss	Bhrd/Bhrd<+>	B6(V)-Bhrd/GrsrJ	N	MGI:3765079
MGI:3766097	F	MP:0002073	abnormal hair growth	Bhrd/Bhrd<+>	B6(V)-Bhrd/GrsrJ	N	MGI:3765079
MGI:3766099	M	MP:0002073	abnormal hair growth	Bhrd/Y	B6(V)-Bhrd/GrsrJ	N	MGI:3765079
MGI:3766099	M	MP:0000416	sparse hair	Bhrd/Y	B6(V)-Bhrd/GrsrJ	N	MGI:3765079
MGI:3766099	M	MP:0001510	abnormal coat appearance	Bhrd/Y	B6(V)-Bhrd/GrsrJ	N	MGI:3765079
MGI:3766260	M	MP:0001379	abnormal penile erection	Immp2l<Tg(Tyr)979Ove>/Immp2l<Tg(Tyr)979Ove>	FVB/N-Immp2l<Tg(Tyr)979Ove>	N	18094351
MGI:3766260	F	MP:0001131	abnormal ovarian follicle morphology	Immp2l<Tg(Tyr)979Ove>/Immp2l<Tg(Tyr)979Ove>	FVB/N-Immp2l<Tg(Tyr)979Ove>	N	18094351
MGI:3766260	F	MP:0001129	impaired ovarian folliculogenesis	Immp2l<Tg(Tyr)979Ove>/Immp2l<Tg(Tyr)979Ove>	FVB/N-Immp2l<Tg(Tyr)979Ove>	N	18094351
MGI:3766260	F	MP:0005431	decreased oocyte number	Immp2l<Tg(Tyr)979Ove>/Immp2l<Tg(Tyr)979Ove>	FVB/N-Immp2l<Tg(Tyr)979Ove>	N	18094351
MGI:3766260	F	MP:0001125	abnormal oocyte morphology	Immp2l<Tg(Tyr)979Ove>/Immp2l<Tg(Tyr)979Ove>	FVB/N-Immp2l<Tg(Tyr)979Ove>	N	18094351
MGI:3766260	M	MP:0002687	oligozoospermia	Immp2l<Tg(Tyr)979Ove>/Immp2l<Tg(Tyr)979Ove>	FVB/N-Immp2l<Tg(Tyr)979Ove>	N	18094351
MGI:3766260	M	MP:0001156	abnormal spermatogenesis	Immp2l<Tg(Tyr)979Ove>/Immp2l<Tg(Tyr)979Ove>	FVB/N-Immp2l<Tg(Tyr)979Ove>	N	18094351
MGI:3766260	M	MP:0001925	male infertility	Immp2l<Tg(Tyr)979Ove>/Immp2l<Tg(Tyr)979Ove>	FVB/N-Immp2l<Tg(Tyr)979Ove>	N	18094351
MGI:3766260	F	MP:0001132	absent mature ovarian follicles	Immp2l<Tg(Tyr)979Ove>/Immp2l<Tg(Tyr)979Ove>	FVB/N-Immp2l<Tg(Tyr)979Ove>	N	18094351
MGI:3766260	F	MP:0001126	abnormal ovary morphology	Immp2l<Tg(Tyr)979Ove>/Immp2l<Tg(Tyr)979Ove>	FVB/N-Immp2l<Tg(Tyr)979Ove>	N	18094351
MGI:3766404	M	MP:0002169	no abnormal phenotype detected	Col4a6<tm1Jrs>/Y	involves: 129	N	17418794
MGI:3766752	F	MP:0001926	female infertility	Del(11Chad-Hoxb1)19Brd/+	involves: 129S7/SvEvBrd * C57BL/6	N	16489219
MGI:3766754	F	MP:0001926	female infertility	Del(11Mpo-Chad)18Brd/+	involves: 129S7/SvEvBrd * C57BL/6	N	16489219
MGI:3767058	M	MP:0011188	increased erythrocyte protoporphyrin level	Heph<sla>/Y	involves: C57BL/6J * WB/Re	N	658175
MGI:3767200	M	MP:0005103	abnormal retina pigmentation	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	15365174
MGI:3767200	M	MP:0014175	abnormal ciliary epithelium morphology	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	18326691
MGI:3767200	M	MP:0005239	abnormal Bruch membrane morphology	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	18326691
MGI:3767200	M	MP:0005201	abnormal retina pigment epithelium morphology	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	18326691
MGI:3767200	M	MP:0001326	retina degeneration	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	15365174
MGI:3767200	M	MP:0001770	abnormal iron level	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	18326691
MGI:3767200	M	MP:0008852	retina neovascularization	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	18326691
MGI:3767200	M	MP:0005549	retina pigment epithelium hyperplasia	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	15365174
MGI:3767200	M	MP:0005549	retina pigment epithelium hyperplasia	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	18326691
MGI:3767200	M	MP:0005201	abnormal retina pigment epithelium morphology	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	15365174
MGI:3767200	M	MP:0001325	abnormal retina morphology	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	18326691
MGI:3767200	M	MP:0001325	abnormal retina morphology	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	15365174
MGI:3767200	M	MP:0031606	increased susceptibility to age-related retinal degeneration	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	18326691
MGI:3767200	M	MP:0001851	eye inflammation	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	18326691
MGI:3767200	M	MP:0008450	retina photoreceptor degeneration	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	15365174
MGI:3767200	M	MP:0008852	retina neovascularization	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	15365174
MGI:3767200	M	MP:0001770	abnormal iron level	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	15365174
MGI:3767200	M	MP:0005098	abnormal optic choroid morphology	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Y	involves: 129X1/SvJ * C57BL/6	N	15365174
MGI:3767204	F	MP:0002447	abnormal erythrocyte morphology	Heph<sla>/Heph<sla>	Not Specified	N	MGI:1889029
MGI:3767204	F	MP:0005562	decreased mean corpuscular hemoglobin	Heph<sla>/Heph<sla>	Not Specified	N	5903585
MGI:3767204	F	MP:0002591	decreased mean corpuscular volume	Heph<sla>/Heph<sla>	Not Specified	N	5903585
MGI:3767204	F	MP:0005097	polychromatophilia	Heph<sla>/Heph<sla>	Not Specified	N	5903585
MGI:3767204	F	MP:0002813	microcytosis	Heph<sla>/Heph<sla>	Not Specified	N	5903585
MGI:3767204	F	MP:0002875	decreased erythrocyte cell number	Heph<sla>/Heph<sla>	Not Specified	N	MGI:1889029
MGI:3767204	F	MP:0008387	hypochromic anemia	Heph<sla>/Heph<sla>	Not Specified	N	5903585
MGI:3767204	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Heph<sla>/Heph<sla>	Not Specified	N	MGI:1889029
MGI:3767204	F	MP:0002874	decreased hemoglobin content	Heph<sla>/Heph<sla>	Not Specified	N	5903585
MGI:3767204	F	MP:0000208	decreased hematocrit	Heph<sla>/Heph<sla>	Not Specified	N	5903585
MGI:3767204	F	MP:0002123	abnormal definitive hematopoiesis	Heph<sla>/Heph<sla>	Not Specified	N	MGI:1889029
MGI:3767204	F	MP:0000248	macrocytosis	Heph<sla>/Heph<sla>	Not Specified	N	5903585
MGI:3767204	F	MP:0002641	anisopoikilocytosis	Heph<sla>/Heph<sla>	Not Specified	N	5903585
MGI:3767204	F	MP:0002875	decreased erythrocyte cell number	Heph<sla>/Heph<sla>	Not Specified	N	5903585
MGI:3767206	M	MP:0005391	vision/eye phenotype	Ocrl<tm2Nbm>/Y	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * NIH Black Swiss)	Y	9593760
MGI:3767206	M	MP:0010768	mortality/aging	Ocrl<tm2Nbm>/Y	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * NIH Black Swiss)	Y	9593760
MGI:3767206	M	MP:0005389	reproductive system phenotype	Ocrl<tm2Nbm>/Y	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * NIH Black Swiss)	Y	9593760
MGI:3767206	M	MP:0005376	homeostasis/metabolism phenotype	Ocrl<tm2Nbm>/Y	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * NIH Black Swiss)	Y	9593760
MGI:3767245	F	MP:0008561	decreased tumor necrosis factor secretion	Tlr7<rsq1>/Tlr7<rsq1>	C57BL/6J-Tlr7<rsq1>	N	MGI:3767030
MGI:3767245	F	MP:0002451	abnormal macrophage physiology	Tlr7<rsq1>/Tlr7<rsq1>	C57BL/6J-Tlr7<rsq1>	N	MGI:3767030
MGI:3767250	M	MP:0002451	abnormal macrophage physiology	Tlr7<rsq1>/Y	C57BL/6J-Tlr7<rsq1>	N	MGI:3767030
MGI:3767250	M	MP:0008561	decreased tumor necrosis factor secretion	Tlr7<rsq1>/Y	C57BL/6J-Tlr7<rsq1>	N	MGI:3767030
MGI:3767257	F	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis	Rorc<tm1Litt>/Rorc<tm1Litt>	involves: 129P2/OlaHsd	N	28846085
MGI:3767262	M	MP:0001380	reduced male mating frequency	Gabrb3<tm2.1Geh>/Gabrb3<tm2.1Geh>,Tg(Camk2a-cre)T29-1Stl/?	involves: 129 * BALB/c * C57BL/6 * SJL	N	17927825
MGI:3767262	F	MP:0001923	reduced female fertility	Gabrb3<tm2.1Geh>/Gabrb3<tm2.1Geh>,Tg(Camk2a-cre)T29-1Stl/?	involves: 129 * BALB/c * C57BL/6 * SJL	N	17927825
MGI:3767262	M	MP:0001922	reduced male fertility	Gabrb3<tm2.1Geh>/Gabrb3<tm2.1Geh>,Tg(Camk2a-cre)T29-1Stl/?	involves: 129 * BALB/c * C57BL/6 * SJL	N	17927825
MGI:3767262	F	MP:0001386	abnormal maternal nurturing	Gabrb3<tm2.1Geh>/Gabrb3<tm2.1Geh>,Tg(Camk2a-cre)T29-1Stl/?	involves: 129 * BALB/c * C57BL/6 * SJL	N	17927825
MGI:3767400	F	MP:0005669	increased circulating leptin level	Tg(HCRT-MJD)1Stak/?	involves: C57BL/6 * DBA/1	N	16626839
MGI:3767400	F	MP:0003212	increased susceptibility to age related obesity	Tg(HCRT-MJD)1Stak/?	involves: C57BL/6 * DBA/1	N	16626839
MGI:3767418	F	MP:0000628	abnormal mammary gland development	Map3k14<aly>/Map3k14<aly>	involves: C57BL/6J	N	10910194
MGI:3767559	M	MP:0008143	abnormal dendrite morphology	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	18093519
MGI:3767559	M	MP:0004851	increased testis weight	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	18093519
MGI:3767559	M	MP:0004000	impaired passive avoidance behavior	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	18093519
MGI:3767559	M	MP:0001496	audiogenic seizures	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	18093519
MGI:3767559	M	MP:0001260	increased body weight	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	18093519
MGI:3767559	M	MP:0009936	abnormal dendritic spine morphology	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	9144249
MGI:3767559	M	MP:0003477	abnormal nerve fiber response	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	18093519
MGI:3767560	M	MP:0002687	oligozoospermia	Celf3<tm1Ade>/Celf3<tm1Ade>	involves: 129S1/Sv * 129X1/SvJ	N	17393433
MGI:3767560	M	MP:0002674	abnormal sperm motility	Celf3<tm1Ade>/Celf3<tm1Ade>	involves: 129S1/Sv * 129X1/SvJ	N	17393433
MGI:3767570	M	MP:0001496	audiogenic seizures	Fmr1<tm1Cgr>/Y,Grm5<tm1Rod>/Grm5<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	18093519
MGI:3767570	M	MP:0003631	nervous system phenotype	Fmr1<tm1Cgr>/Y,Grm5<tm1Rod>/Grm5<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB	Y	18093519
MGI:3767570	M	MP:0004851	increased testis weight	Fmr1<tm1Cgr>/Y,Grm5<tm1Rod>/Grm5<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	18093519
MGI:3767570	M	MP:0005386	behavior/neurological phenotype	Fmr1<tm1Cgr>/Y,Grm5<tm1Rod>/Grm5<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB	Y	18093519
MGI:3767570	M	MP:0005378	growth/size/body region phenotype	Fmr1<tm1Cgr>/Y,Grm5<tm1Rod>/Grm5<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB	Y	18093519
MGI:3767641	M	MP:0001156	abnormal spermatogenesis	Bub1<tm1Ssta>/Bub1<tm1Ssta>,Tg(CAG-cre/Esr1*)5Amc/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	17925231
MGI:3767641	M	MP:0001925	male infertility	Bub1<tm1Ssta>/Bub1<tm1Ssta>,Tg(CAG-cre/Esr1*)5Amc/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	17925231
MGI:3767641	M	MP:0004852	decreased testis weight	Bub1<tm1Ssta>/Bub1<tm1Ssta>,Tg(CAG-cre/Esr1*)5Amc/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	17925231
MGI:3767641	M	MP:0001153	small seminiferous tubules	Bub1<tm1Ssta>/Bub1<tm1Ssta>,Tg(CAG-cre/Esr1*)5Amc/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	17925231
MGI:3767641	M	MP:0002687	oligozoospermia	Bub1<tm1Ssta>/Bub1<tm1Ssta>,Tg(CAG-cre/Esr1*)5Amc/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	17925231
MGI:3767679	M	MP:0008545	absent sperm flagellum	Bbs1<tm1Vcs>/Bbs1<tm1Vcs>	involves: 129S1/Sv * 129X1/SvJ	N	18032602
MGI:3767679	M	MP:0001925	male infertility	Bbs1<tm1Vcs>/Bbs1<tm1Vcs>	involves: 129S1/Sv * 129X1/SvJ	N	18032602
MGI:3767835	M	MP:0001925	male infertility	mn/mn	involves: AKR-T stock * brachy stock	N	MGI:61285
MGI:3767835	F	MP:0001926	female infertility	mn/mn	involves: AKR-T stock * brachy stock	N	MGI:61285
MGI:3767994	F	MP:0001926	female infertility	mc/mc	C57BL/10ScBs-mc	N	MGI:63135
MGI:3768233	M	MP:0004901	decreased male germ cell number	Nanos2<tm3Ysa>/Nanos2<tm3Ysa>	involves: C57BL/6 * CBA * ICR	N	16806845
MGI:3768233	M	MP:0001156	abnormal spermatogenesis	Nanos2<tm3Ysa>/Nanos2<tm3Ysa>	involves: C57BL/6 * CBA * ICR	N	16806845
MGI:3768233	M	MP:0002216	abnormal seminiferous tubule morphology	Nanos2<tm3Ysa>/Nanos2<tm3Ysa>	involves: C57BL/6 * CBA * ICR	N	16806845
MGI:3768235	M	MP:0001156	abnormal spermatogenesis	Nanos2<tm1Ysa>/Nanos2<tm3Ysa>	involves: 129 * C57BL/6 * CBA * ICR	N	16806845
MGI:3768235	M	MP:0004901	decreased male germ cell number	Nanos2<tm1Ysa>/Nanos2<tm3Ysa>	involves: 129 * C57BL/6 * CBA * ICR	N	16806845
MGI:3768235	M	MP:0002216	abnormal seminiferous tubule morphology	Nanos2<tm1Ysa>/Nanos2<tm3Ysa>	involves: 129 * C57BL/6 * CBA * ICR	N	16806845
MGI:3768252	M	MP:0002874	decreased hemoglobin content	Heph<sla>/Y	B6.Cg-Heph<sla>	N	708646
MGI:3768252	M	MP:0004265	abnormal placental transport	Heph<sla>/Y	B6.Cg-Heph<sla>	N	708646
MGI:3768252	M	MP:0001577	anemia	Heph<sla>/Y	B6.Cg-Heph<sla>	N	708646
MGI:3768252	M	MP:0001770	abnormal iron level	Heph<sla>/Y	B6.Cg-Heph<sla>	N	708646
MGI:3768252	M	MP:0005637	abnormal iron homeostasis	Heph<sla>/Y	B6.Cg-Heph<sla>	N	180329
MGI:3768260	F	MP:0001770	abnormal iron level	Heph<sla>/Heph<sla>	B6.Cg-Heph<sla>	N	708646
MGI:3768260	F	MP:0002874	decreased hemoglobin content	Heph<sla>/Heph<sla>	B6.Cg-Heph<sla>	N	708646
MGI:3768260	F	MP:0004265	abnormal placental transport	Heph<sla>/Heph<sla>	B6.Cg-Heph<sla>	N	708646
MGI:3768260	F	MP:0001577	anemia	Heph<sla>/Heph<sla>	B6.Cg-Heph<sla>	N	708646
MGI:3768517	F	MP:0002566	abnormal sexual interaction	Tg(Prnp-MAPT*P301S)PS19Vle/Tg(Prnp-MAPT*P301S)PS19Vle	involves: C3H * C57BL/6	N	17270732
MGI:3768518	F	MP:0001463	abnormal spatial learning	Tg(Prnp-MAPT*P301S)PS19Vle/0	involves: C3H * C57BL/6	N	21698260
MGI:3768529	M	MP:0001925	male infertility	Jam3<tm1Rha>/Jam3<tm1Rha>,Tg(Tek-Jam3)1Maal/?	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA	N	17455169
MGI:3768564	F	MP:0001119	abnormal female reproductive system morphology	Pgr<tm3(rtTA2S*M2)Lyd>/Pgr<tm3(rtTA2S*M2)Lyd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17941046
MGI:3768564	F	MP:0001926	female infertility	Pgr<tm3(rtTA2S*M2)Lyd>/Pgr<tm3(rtTA2S*M2)Lyd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17941046
MGI:3768762	F	MP:0001926	female infertility	Hi/Hi	involves: C57BL/6 * CBA	N	MGI:61686
MGI:3768765	M	MP:0009237	kinked sperm flagellum	Herc4<Gt(RRH224)Byg>/Herc4<Gt(RRH224)Byg>	Not Specified	N	17967448
MGI:3768765	M	MP:0001155	arrest of spermatogenesis	Herc4<Gt(RRH224)Byg>/Herc4<Gt(RRH224)Byg>	Not Specified	N	17967448
MGI:3768765	M	MP:0002675	asthenozoospermia	Herc4<Gt(RRH224)Byg>/Herc4<Gt(RRH224)Byg>	Not Specified	N	17967448
MGI:3768765	M	MP:0001922	reduced male fertility	Herc4<Gt(RRH224)Byg>/Herc4<Gt(RRH224)Byg>	Not Specified	N	17967448
MGI:3768910	M	MP:0008261	arrest of male meiosis	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	N	17425408
MGI:3768910	F	MP:0005168	abnormal female meiosis	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	N	17425408
MGI:3768910	M	MP:0006379	abnormal spermatocyte morphology	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	N	17425408
MGI:3768910	F	MP:0001923	reduced female fertility	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	N	17425408
MGI:3768910	F	MP:0005431	decreased oocyte number	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	N	17425408
MGI:3768910	M	MP:0001925	male infertility	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	N	17425408
MGI:3768910	F	MP:0001131	abnormal ovarian follicle morphology	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	N	17425408
MGI:3768911	M	MP:0001925	male infertility	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C57BL/6J	N	17425408
MGI:3768911	M	MP:0008261	arrest of male meiosis	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C57BL/6J	N	17425408
MGI:3768911	F	MP:0001131	abnormal ovarian follicle morphology	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C57BL/6J	N	17425408
MGI:3768911	F	MP:0005168	abnormal female meiosis	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C57BL/6J	N	17425408
MGI:3768914	M	MP:0008261	arrest of male meiosis	Dmc1<tm1Jcs>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	N	17425408
MGI:3768914	M	MP:0006379	abnormal spermatocyte morphology	Dmc1<tm1Jcs>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	N	17425408
MGI:3768914	F	MP:0005431	decreased oocyte number	Dmc1<tm1Jcs>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	N	17425408
MGI:3768914	F	MP:0002777	absent ovarian follicles	Dmc1<tm1Jcs>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	N	17425408
MGI:3768914	F	MP:0001131	abnormal ovarian follicle morphology	Dmc1<tm1Jcs>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	N	17425408
MGI:3768914	F	MP:0001926	female infertility	Dmc1<tm1Jcs>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	N	17425408
MGI:3769353	F	MP:0008826	abnormal splenic cell ratio	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>	B6.129S4-Il2rg<tm1Wjl>/J	N	16020505
MGI:3769353	F	MP:0008122	decreased myeloid dendritic cell number	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>	B6.129S4-Il2rg<tm1Wjl>/J	N	16020505
MGI:3769353	F	MP:0002376	abnormal dendritic cell physiology	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>	B6.129S4-Il2rg<tm1Wjl>/J	N	16020505
MGI:3769364	F	MP:0003579	increased ovarian carcinoma incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2.1Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	17967875
MGI:3769364	F	MP:0008000	increased ovary tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2.1Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	17967875
MGI:3769364	M	MP:0006262	increased testis tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2.1Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	17967875
MGI:3769364	M	MP:0001925	male infertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2.1Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	17967875
MGI:3769365	M	MP:0001925	male infertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S/SvEv * C57BL/6	N	17967875
MGI:3769365	F	MP:0008000	increased ovary tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S/SvEv * C57BL/6	N	17967875
MGI:3769365	F	MP:0003579	increased ovarian carcinoma incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S/SvEv * C57BL/6	N	17967875
MGI:3769365	M	MP:0006262	increased testis tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S/SvEv * C57BL/6	N	17967875
MGI:3769366	M	MP:0006262	increased testis tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Zuk>	involves: 129P2/OlaHsd * 129S/SvEv * 129S7/SvEvBrd * C57BL/6	N	17967875
MGI:3769366	F	MP:0008000	increased ovary tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Zuk>	involves: 129P2/OlaHsd * 129S/SvEv * 129S7/SvEvBrd * C57BL/6	N	17967875
MGI:3769366	M	MP:0001925	male infertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Zuk>	involves: 129P2/OlaHsd * 129S/SvEv * 129S7/SvEvBrd * C57BL/6	N	17967875
MGI:3769366	F	MP:0003579	increased ovarian carcinoma incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Zuk>	involves: 129P2/OlaHsd * 129S/SvEv * 129S7/SvEvBrd * C57BL/6	N	17967875
MGI:3769375	F	MP:0008995	early reproductive senescence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Zuk>,Smad9<tm1Jfm>/Smad9<tm1Jfm>	involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6	N	17967875
MGI:3769375	F	MP:0008000	increased ovary tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Zuk>,Smad9<tm1Jfm>/Smad9<tm1Jfm>	involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6	N	17967875
MGI:3769375	F	MP:0003579	increased ovarian carcinoma incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Zuk>,Smad9<tm1Jfm>/Smad9<tm1Jfm>	involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6	N	17967875
MGI:3769375	F	MP:0005435	hemoperitoneum	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Zuk>,Smad9<tm1Jfm>/Smad9<tm1Jfm>	involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6	N	17967875
MGI:3769400	M	MP:0005459	decreased percent body fat/body weight	Slc30a7<Gt(XC827)Byg>/Slc30a7<Gt(XC827)Byg>	B6.129P2-Slc30a7<Gt(XC827)Byg>	N	17954933
MGI:3769400	M	MP:0011940	decreased food intake	Slc30a7<Gt(XC827)Byg>/Slc30a7<Gt(XC827)Byg>	B6.129P2-Slc30a7<Gt(XC827)Byg>	N	17954933
MGI:3769414	F	MP:0001120	abnormal uterus morphology	Errfi1<tm1.1Jwj>/Errfi1<tm1.1Jwj>	involves: 129 * C57BL/6 * FVB/N * SJL	N	17987665
MGI:3769414	F	MP:0004904	increased uterus weight	Errfi1<tm1.1Jwj>/Errfi1<tm1.1Jwj>	involves: 129 * C57BL/6 * FVB/N * SJL	N	17987665
MGI:3769414	F	MP:0009092	endometrium hyperplasia	Errfi1<tm1.1Jwj>/Errfi1<tm1.1Jwj>	involves: 129 * C57BL/6 * FVB/N * SJL	N	17987665
MGI:3769419	M	MP:0006380	abnormal spermatid morphology	Cadm1<tm1Momo>/Cadm1<tm1Momo>	involves: 129S/SvEv * C57BL/6J	N	16382161
MGI:3769419	M	MP:0004901	decreased male germ cell number	Cadm1<tm1Momo>/Cadm1<tm1Momo>	involves: 129S/SvEv * C57BL/6J	N	16382161
MGI:3769419	M	MP:0001925	male infertility	Cadm1<tm1Momo>/Cadm1<tm1Momo>	involves: 129S/SvEv * C57BL/6J	N	16382161
MGI:3769419	M	MP:0002687	oligozoospermia	Cadm1<tm1Momo>/Cadm1<tm1Momo>	involves: 129S/SvEv * C57BL/6J	N	16382161
MGI:3769419	M	MP:0008279	arrest of spermiogenesis	Cadm1<tm1Momo>/Cadm1<tm1Momo>	involves: 129S/SvEv * C57BL/6J	N	16382161
MGI:3769419	M	MP:0002675	asthenozoospermia	Cadm1<tm1Momo>/Cadm1<tm1Momo>	involves: 129S/SvEv * C57BL/6J	N	16382161
MGI:3769419	M	MP:0005578	teratozoospermia	Cadm1<tm1Momo>/Cadm1<tm1Momo>	involves: 129S/SvEv * C57BL/6J	N	16382161
MGI:3769419	M	MP:0004850	abnormal testis weight	Cadm1<tm1Momo>/Cadm1<tm1Momo>	involves: 129S/SvEv * C57BL/6J	N	16382161
MGI:3769420	M	MP:0006380	abnormal spermatid morphology	Cadm1<tm1Momo>/Cadm1<tm1Momo>	involves: 129S/SvEv	N	18055550
MGI:3769498	M	MP:0004478	increased testicular teratoma incidence	Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	N	16227443
MGI:3769499	M	MP:0004478	increased testicular teratoma incidence	Trp53<tm1Tyj>/Trp53<tm1Tyj>	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	N	16227443
MGI:3770031	M	MP:0000248	macrocytosis	Heph<sla>/Y	Not Specified	N	5903585
MGI:3770031	M	MP:0002591	decreased mean corpuscular volume	Heph<sla>/Y	Not Specified	N	5903585
MGI:3770031	M	MP:0002813	microcytosis	Heph<sla>/Y	Not Specified	N	5903585
MGI:3770031	M	MP:0005097	polychromatophilia	Heph<sla>/Y	Not Specified	N	5903585
MGI:3770031	M	MP:0002875	decreased erythrocyte cell number	Heph<sla>/Y	Not Specified	N	5903585
MGI:3770031	M	MP:0000208	decreased hematocrit	Heph<sla>/Y	Not Specified	N	5903585
MGI:3770031	M	MP:0008387	hypochromic anemia	Heph<sla>/Y	Not Specified	N	5903585
MGI:3770031	M	MP:0002874	decreased hemoglobin content	Heph<sla>/Y	Not Specified	N	5903585
MGI:3770031	M	MP:0005562	decreased mean corpuscular hemoglobin	Heph<sla>/Y	Not Specified	N	5903585
MGI:3770031	M	MP:0002641	anisopoikilocytosis	Heph<sla>/Y	Not Specified	N	5903585
MGI:3770054	F	MP:0002118	abnormal lipid homeostasis	Thrsp<tm1Cnm>/Thrsp<tm1Cnm>	B6.129-Thrsp<tm1Cnm>	N	15890771
MGI:3770054	F	MP:0001882	abnormal lactation	Thrsp<tm1Cnm>/Thrsp<tm1Cnm>	B6.129-Thrsp<tm1Cnm>	N	15890771
MGI:3770054	F	MP:0004047	abnormal milk composition	Thrsp<tm1Cnm>/Thrsp<tm1Cnm>	B6.129-Thrsp<tm1Cnm>	N	15890771
MGI:3770280	F	MP:0003845	abnormal decidualization	Tg(IGFBP1)2Miel/0	CBACa.Cg-Tg(IGFBP1)2Miel	N	12163461
MGI:3770280	F	MP:0004256	abnormal maternal decidual layer morphology	Tg(IGFBP1)2Miel/0	CBACa.Cg-Tg(IGFBP1)2Miel	N	12163461
MGI:3770611	F	MP:0002680	decreased corpora lutea number	Lepr<db-9J>/Lepr<db-9J>	involves: C57BL/6 * CBA * SWR	N	MGI:3770514
MGI:3770611	F	MP:0002682	decreased mature ovarian follicle number	Lepr<db-9J>/Lepr<db-9J>	involves: C57BL/6 * CBA * SWR	N	MGI:3770514
MGI:3770611	F	MP:0001923	reduced female fertility	Lepr<db-9J>/Lepr<db-9J>	involves: C57BL/6 * CBA * SWR	N	MGI:3770514
MGI:3770611	F	MP:0005431	decreased oocyte number	Lepr<db-9J>/Lepr<db-9J>	involves: C57BL/6 * CBA * SWR	N	MGI:3770514
MGI:3770616	F	MP:0008000	increased ovary tumor incidence	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm2Tyj>/Kras<+>	involves: 129S2/SvPas * C57BL/6	N	17936562
MGI:3770650	M	MP:0002075	abnormal coat/hair pigmentation	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	N	9427628
MGI:3770650	M	MP:0005389	reproductive system phenotype	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	Y	9427628
MGI:3770650	M	MP:0000583	long toenails	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	N	9427628
MGI:3770650	M	MP:0001349	excessive tearing	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	N	9427628
MGI:3770650	M	MP:0010768	mortality/aging	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	Y	9427628
MGI:3770650	M	MP:0002066	abnormal motor capabilities/coordination/movement	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	N	9427628
MGI:3770650	M	MP:0001265	decreased body size	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	N	9427628
MGI:3770650	M	MP:0002961	abnormal axon guidance	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	N	9427628
MGI:3770650	M	MP:0008489	slow postnatal weight gain	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	N	9427628
MGI:3770650	M	MP:0011101	prenatal lethality, incomplete penetrance	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	N	9427628
MGI:3770650	M	MP:0000755	hindlimb paralysis	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	N	9427628
MGI:3770650	M	MP:0001925	male infertility	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	N	9427628
MGI:3770650	M	MP:0002878	abnormal corticospinal tract morphology	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	N	9427628
MGI:3770650	M	MP:0006198	enophthalmos	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	N	9427628
MGI:3770650	M	MP:0003631	nervous system phenotype	L1cam<tm1Sor>/Y	either: 129S7/SvEvBrd-L1cam<tm1Sor> or (129S7/SvEvBrd * C57BL/6J)F1	Y	9427628
MGI:3770657	F	MP:0008211	decreased mature B cell number	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0002460	decreased immunoglobulin level	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0008215	decreased immature B cell number	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0000703	abnormal thymus morphology	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0002078	abnormal glucose homeostasis	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	18563383
MGI:3770657	F	MP:0001559	hyperglycemia	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	18563383
MGI:3770657	F	MP:0002879	increased cellular sensitivity to X-ray irradiation	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0008826	abnormal splenic cell ratio	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0002217	small lymph nodes	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0005671	abnormal response to transplant	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0000221	decreased leukocyte cell number	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0002083	premature death	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0008101	lymph node hypoplasia	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0014130	thymus cyst	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0002591	decreased mean corpuscular volume	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0008045	decreased NK cell number	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0004503	decreased incidence of tumors by ionizing radiation induction	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0002722	abnormal immune system organ morphology	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770657	F	MP:0014263	decreased spleen B cell follicle number	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770661	M	MP:0001262	decreased body weight	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770661	M	MP:0001463	abnormal spatial learning	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770661	M	MP:0000968	abnormal sensory neuron innervation pattern	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	18550718
MGI:3770661	M	MP:0002557	abnormal social/conspecific interaction behavior	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770661	M	MP:0003651	abnormal axon extension	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770661	M	MP:0002152	abnormal brain morphology	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770661	M	MP:0000825	dilated lateral ventricle	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770661	M	MP:0001402	decreased locomotor activity	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770661	M	MP:0005537	abnormal cerebral aqueduct morphology	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770661	M	MP:0001405	impaired coordination	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770661	M	MP:0000849	abnormal cerebellum morphology	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770661	M	MP:0008534	enlarged fourth ventricle	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770661	M	MP:0000828	abnormal fourth ventricle morphology	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770661	M	MP:0006282	abnormal spinal cord dorsal horn morphology	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	18550718
MGI:3770661	M	MP:0005423	abnormal somatic nervous system physiology	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	18550718
MGI:3770661	M	MP:0000866	cerebellum vermis hypoplasia	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770661	M	MP:0002797	increased thigmotaxis	L1cam<tm1Sor>/Y	involves: 129S7/SvEvBrd	N	9580664
MGI:3770662	M	MP:0008826	abnormal splenic cell ratio	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0002217	small lymph nodes	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0002879	increased cellular sensitivity to X-ray irradiation	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0008211	decreased mature B cell number	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0000221	decreased leukocyte cell number	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0008045	decreased NK cell number	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0002722	abnormal immune system organ morphology	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0005671	abnormal response to transplant	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0005671	abnormal response to transplant	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	18785974
MGI:3770662	M	MP:0002083	premature death	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0008101	lymph node hypoplasia	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0002591	decreased mean corpuscular volume	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0008215	decreased immature B cell number	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0014263	decreased spleen B cell follicle number	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0002460	decreased immunoglobulin level	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770662	M	MP:0000703	abnormal thymus morphology	Il2rg<tm1Wjl>/Y,Prkdc<scid>/Prkdc<scid>	NOD.Cg-Prkdc<scid> Il2rg<tm1Wjl>/Sz	N	15879151
MGI:3770780	F	MP:0006361	abnormal female germ cell morphology	Kit<tm1Alf>/Kit<tm1Alf>	involves: 129S2/SvPas	N	8898216
MGI:3770811	F	MP:0001130	abnormal ovarian folliculogenesis	Kit<tm1Alf>/Kit<+>	involves: 129S2/SvPas	N	11226047
MGI:3770811	M	MP:0004929	decreased epididymis weight	Kit<tm1Alf>/Kit<+>	involves: 129S2/SvPas	N	12406368
MGI:3770811	M	MP:0006362	abnormal male germ cell morphology	Kit<tm1Alf>/Kit<+>	involves: 129S2/SvPas	N	12406368
MGI:3770811	M	MP:0001922	reduced male fertility	Kit<tm1Alf>/Kit<+>	involves: 129S2/SvPas	N	12406368
MGI:3770811	M	MP:0001145	abnormal male reproductive system morphology	Kit<tm1Alf>/Kit<+>	involves: 129S2/SvPas	N	12406368
MGI:3770811	M	MP:0004852	decreased testis weight	Kit<tm1Alf>/Kit<+>	involves: 129S2/SvPas	N	12406368
MGI:3770811	M	MP:0002675	asthenozoospermia	Kit<tm1Alf>/Kit<+>	involves: 129S2/SvPas	N	12406368
MGI:3770811	F	MP:0001119	abnormal female reproductive system morphology	Kit<tm1Alf>/Kit<+>	involves: 129S2/SvPas	N	11226047
MGI:3770811	F	MP:0008871	abnormal ovarian follicle number	Kit<tm1Alf>/Kit<+>	involves: 129S2/SvPas	N	11226047
MGI:3770811	M	MP:0002687	oligozoospermia	Kit<tm1Alf>/Kit<+>	involves: 129S2/SvPas	N	12406368
MGI:3770811	F	MP:0001125	abnormal oocyte morphology	Kit<tm1Alf>/Kit<+>	involves: 129S2/SvPas	N	11226047
MGI:3770811	F	MP:0011121	decreased primordial ovarian follicle number	Kit<tm1Alf>/Kit<+>	involves: 129S2/SvPas	N	11226047
MGI:3771037	M	MP:0008880	lacrimal gland inflammation	Aec1<NOD/Uf>/Aec1<NOD/Uf>,Aec2<NOD/Uf>/Aec2<NOD/Uf>	B6.NOD-Aec2<NOD/Uf> Aec1<NOD/Uf>	N	16918699
MGI:3771183	F	MP:0004898	uterine hemorrhage	Fgg<tm1Lord>/Fgg<tm1Lord>	involves: 129P2/OlaHsd * C57BL/6	N	15304068
MGI:3771183	F	MP:0001926	female infertility	Fgg<tm1Lord>/Fgg<tm1Lord>	involves: 129P2/OlaHsd * C57BL/6	N	15304068
MGI:3771211	F	MP:0012009	early parturition	Hpgd<tm1Ljm>/Hpgd<tm1Ljm>	involves: 129S6/SvEvTac * C57BL/6	N	17872381
MGI:3771211	F	MP:0002679	abnormal corpus luteum morphology	Hpgd<tm1Ljm>/Hpgd<tm1Ljm>	involves: 129S6/SvEvTac * C57BL/6	N	17872381
MGI:3771212	F	MP:0012009	early parturition	Hpgd<tm1Ljm>/Hpgd<+>	involves: 129S6/SvEvTac * C57BL/6	N	17872381
MGI:3771293	F	MP:0002907	abnormal parturition	Oxt<tm2Ljm>/Oxt<tm2Ljm>	B6.129S2-Oxt<tm2Ljm>	N	17895964
MGI:3771294	F	MP:0002907	abnormal parturition	Oxt<tm3Ljm>/Oxt<tm3Ljm>	either: B6.129S2-Oxt<tm3Ljm> or B6.129S6-Oxt<tm3Ljm>	N	17895964
MGI:3771294	F	MP:0008028	pregnancy-related premature death	Oxt<tm3Ljm>/Oxt<tm3Ljm>	either: B6.129S2-Oxt<tm3Ljm> or B6.129S6-Oxt<tm3Ljm>	N	17895964
MGI:3771333	F	MP:0000662	abnormal branching of the mammary ductal tree	B4galt1<tm2Shur>/B4galt1<tm2Shur>	involves: 129S7/SvEvBrd * C57BL/6J	N	11900463
MGI:3771333	F	MP:0006269	abnormal mammary gland growth during pregnancy	B4galt1<tm2Shur>/B4galt1<tm2Shur>	involves: 129S7/SvEvBrd * C57BL/6J	N	11900463
MGI:3771333	M	MP:0004542	impaired acrosome reaction	B4galt1<tm2Shur>/B4galt1<tm2Shur>	involves: 129S7/SvEvBrd * C57BL/6J	N	9374408
MGI:3771333	F	MP:0004047	abnormal milk composition	B4galt1<tm2Shur>/B4galt1<tm2Shur>	involves: 129S7/SvEvBrd * C57BL/6J	N	11900463
MGI:3771372	F	MP:0001883	increased mammary adenocarcinoma incidence	Stat1<tm1Rds>/Stat1<tm1Rds>	129S6/SvEv-Stat1<tm1Rds>/Tac	N	22264274
MGI:3771561	F	MP:0001119	abnormal female reproductive system morphology	jg/jg	C3H/HeJ-jg	N	MGI:61614
MGI:3771561	M	MP:0001925	male infertility	jg/jg	C3H/HeJ-jg	N	MGI:61614
MGI:3771561	M	MP:0001146	abnormal testis morphology	jg/jg	C3H/HeJ-jg	N	MGI:61614
MGI:3771561	F	MP:0001127	small ovary	jg/jg	C3H/HeJ-jg	N	MGI:61614
MGI:3771561	M	MP:0001147	small testis	jg/jg	C3H/HeJ-jg	N	MGI:61614
MGI:3771561	M	MP:0004849	abnormal testis size	jg/jg	C3H/HeJ-jg	N	MGI:61614
MGI:3771561	M	MP:0003698	abnormal male reproductive system physiology	jg/jg	C3H/HeJ-jg	N	MGI:61614
MGI:3771561	F	MP:0004853	abnormal ovary size	jg/jg	C3H/HeJ-jg	N	MGI:61614
MGI:3771561	F	MP:0001923	reduced female fertility	jg/jg	C3H/HeJ-jg	N	MGI:61614
MGI:3771571	M	MP:0004933	abnormal epididymis epithelium morphology	Inhba<tm1Zuk>/Inhba<tm1Zuk>	involves: 129S7/SvEvBrd	N	17592132
MGI:3771571	M	MP:0002631	abnormal epididymis morphology	Inhba<tm1Zuk>/Inhba<tm1Zuk>	involves: 129S7/SvEvBrd	N	17592132
MGI:3771612	M	MP:0002472	impaired complement alternative pathway	Cfp<tm1Song>/Y	involves: 129 * C57BL/6	N	17916747
MGI:3771612	M	MP:0002473	impaired complement classical pathway	Cfp<tm1Song>/Y	involves: 129 * C57BL/6	N	17916747
MGI:3771612	M	MP:0002471	abnormal complement pathway	Cfp<tm1Song>/Y	involves: 129 * C57BL/6	N	17916747
MGI:3771613	M	MP:0002169	no abnormal phenotype detected	Cfp<tm1.1Song>/Y	involves: 129 * C57BL/6 * SJL	N	17916747
MGI:3771618	M	MP:0011939	increased food intake	Arid5b<tm1Whit>/Arid5b<+>	involves: 129S1/Sv * C57BL/6J	N	14651970
MGI:3771618	F	MP:0011940	decreased food intake	Arid5b<tm1Whit>/Arid5b<+>	involves: 129S1/Sv * C57BL/6J	N	14651970
MGI:3771709	M	MP:0001156	abnormal spermatogenesis	Kit<tm1Alf>/Kit<Mhdasow3>	involves: 129S2/SvPas * C3HeB/FeJ	N	17612398
MGI:3771809	F	MP:0001728	failure of embryo implantation	Vezt<tm1.1Smc>/Vezt<tm1.1Smc>	either: (involves: 129S2/SvPas * BALB/c * C57BL/6 * MF1) or (involves: 129S2/SvPas * BALB/c * C57BL/6 * C57BL/6N * MF1)	N	17452094
MGI:3771855	F	MP:0000662	abnormal branching of the mammary ductal tree	Phb1<Gt(XT0035)Wtsi>/Phb1<+>	involves: 129P2/OlaHsd * C57BL	N	17932104
MGI:3771857	F	MP:0000662	abnormal branching of the mammary ductal tree	Phb1<Gt(BGB069)Byg>/Phb1<+>	involves: 129P2/OlaHsd * C57BL	N	17932104
MGI:3772358	M	MP:0003960	increased lean body mass	Bcat2<tm1.2Clyn>/Bcat2<tm1.2Clyn>	involves: BALB/cJ * C57BL/6J * C57BL/6N	N	17767905
MGI:3772358	M	MP:0005459	decreased percent body fat/body weight	Bcat2<tm1.2Clyn>/Bcat2<tm1.2Clyn>	involves: BALB/cJ * C57BL/6J * C57BL/6N	N	17767905
MGI:3772358	M	MP:0003068	enlarged kidney	Bcat2<tm1.2Clyn>/Bcat2<tm1.2Clyn>	involves: BALB/cJ * C57BL/6J * C57BL/6N	N	17767905
MGI:3772358	M	MP:0001432	abnormal food preference	Bcat2<tm1.2Clyn>/Bcat2<tm1.2Clyn>	involves: BALB/cJ * C57BL/6J * C57BL/6N	N	17767905
MGI:3772358	M	MP:0005418	abnormal circulating hormone level	Bcat2<tm1.2Clyn>/Bcat2<tm1.2Clyn>	involves: BALB/cJ * C57BL/6J * C57BL/6N	N	17767905
MGI:3772358	M	MP:0005668	decreased circulating leptin level	Bcat2<tm1.2Clyn>/Bcat2<tm1.2Clyn>	involves: BALB/cJ * C57BL/6J * C57BL/6N	N	17767905
MGI:3772446	M	MP:0005466	abnormal T-helper 2 physiology	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	N	18066066
MGI:3772446	M	MP:0005025	abnormal response to infection	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	N	18066066
MGI:3772446	M	MP:0005026	decreased susceptibility to parasitic infection	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	N	18066066
MGI:3772446	M	MP:0008090	increased T-helper 2 cell number	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	N	18066066
MGI:3772446	M	MP:0008626	increased circulating interleukin-5 level	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	N	18066066
MGI:3772446	M	MP:0002495	increased IgA level	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	N	18066066
MGI:3772446	M	MP:0005011	increased eosinophil cell number	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	N	18066066
MGI:3772446	M	MP:0008074	increased CD4-positive, alpha-beta T cell number	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	N	18066066
MGI:3772446	M	MP:0003957	abnormal nitric oxide homeostasis	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	N	18066066
MGI:3772446	M	MP:0008499	increased IgG1 level	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	N	18066066
MGI:3772446	M	MP:0010768	mortality/aging	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	Y	18066066
MGI:3772446	M	MP:0002335	decreased airway responsiveness	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	N	18066066
MGI:3772446	M	MP:0008502	increased IgG3 level	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	N	18066066
MGI:3772446	M	MP:0002492	decreased IgE level	Il13ra1<tm1Twy>/Y	C.Cg-Il13ra1<tm1Twy>	N	18066066
MGI:3772447	M	MP:0002083	premature death	mgb/mgb	involves: C57BL/6 * FVB/N	N	17202422
MGI:3772447	M	MP:0005565	increased blood urea nitrogen level	mgb/mgb	involves: C57BL/6 * FVB/N	N	17202422
MGI:3772447	M	MP:0001562	abnormal circulating calcium level	mgb/mgb	involves: C57BL/6 * FVB/N	N	17202422
MGI:3772447	M	MP:0005553	increased circulating creatinine level	mgb/mgb	involves: C57BL/6 * FVB/N	N	17202422
MGI:3772447	M	MP:0005627	increased circulating potassium level	mgb/mgb	involves: C57BL/6 * FVB/N	N	17202422
MGI:3772447	M	MP:0001756	abnormal urination	mgb/mgb	involves: C57BL/6 * FVB/N	N	17202422
MGI:3772448	M	MP:0003019	increased circulating chloride level	mgb/0	involves: C57BL/6 * FVB/N	N	17202422
MGI:3772448	M	MP:0005627	increased circulating potassium level	mgb/0	involves: C57BL/6 * FVB/N	N	17202422
MGI:3772457	M	MP:0002052	decreased tumor incidence	Tg(CAG-SAC/EGFP)35Rang/0,Tg(TRAMP)8247Ng/0	involves: C3H * C57BL/6	N	17909035
MGI:3772457	M	MP:0006042	increased apoptosis	Tg(CAG-SAC/EGFP)35Rang/0,Tg(TRAMP)8247Ng/0	involves: C3H * C57BL/6	N	17909035
MGI:3772458	M	MP:0004961	increased prostate gland weight	Tg(TRAMP)8247Ng/0	involves: C3H * C57BL/6	N	17909035
MGI:3772458	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(TRAMP)8247Ng/0	involves: C3H * C57BL/6	N	17909035
MGI:3772458	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(TRAMP)8247Ng/0	involves: C3H * C57BL/6	N	17909035
MGI:3772458	M	MP:0010357	increased prostate gland tumor incidence	Tg(TRAMP)8247Ng/0	involves: C3H * C57BL/6	N	17909035
MGI:3772558	M	MP:0004158	right aortic arch	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0004110	transposition of great arteries	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0005312	pericardial effusion	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0000285	abnormal heart valve morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0006126	abnormal cardiac outflow tract development	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0002747	abnormal aortic valve morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0010449	heart right ventricle outflow tract stenosis	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0004160	retroesophageal right subclavian artery	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0009845	abnormal neural crest cell morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0000274	enlarged heart	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0000266	abnormal heart morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0011659	interrupted aortic arch, type b	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0003920	abnormal heart right ventricle morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0004157	interrupted aortic arch	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0031517	interrupted aortic arch, type c	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0001785	edema	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0002633	persistent truncus arteriosus	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0000286	abnormal mitral valve morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0000428	abnormal craniofacial morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0001698	decreased embryo size	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0006128	pulmonary valve stenosis	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0000284	double outlet right ventricle	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0004113	abnormal aortic arch morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0011262	abnormal pharyngeal arch mesenchyme morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0002925	abnormal cardiovascular development	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0000273	overriding aortic valve	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0006138	congestive heart failure	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772558	M	MP:0010402	ventricular septal defect	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0000428	abnormal craniofacial morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0004160	retroesophageal right subclavian artery	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0000266	abnormal heart morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0006138	congestive heart failure	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0006126	abnormal cardiac outflow tract development	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0005312	pericardial effusion	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0002925	abnormal cardiovascular development	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0004110	transposition of great arteries	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0004113	abnormal aortic arch morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	M	MP:0031517	interrupted aortic arch, type c	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0001785	edema	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0000285	abnormal heart valve morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0002633	persistent truncus arteriosus	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0010449	heart right ventricle outflow tract stenosis	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0010402	ventricular septal defect	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0001698	decreased embryo size	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0000286	abnormal mitral valve morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0004157	interrupted aortic arch	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0011659	interrupted aortic arch, type b	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0000274	enlarged heart	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0006128	pulmonary valve stenosis	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0009845	abnormal neural crest cell morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0000284	double outlet right ventricle	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0004158	right aortic arch	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0011262	abnormal pharyngeal arch mesenchyme morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0000273	overriding aortic valve	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0002747	abnormal aortic valve morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772559	F	MP:0003920	abnormal heart right ventricle morphology	Hprt1<tm2(Pgk1-Pac/TK)Brd>/Hprt1<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S7/SvEvBrd * C57BL/6 * CBA	N	18058916
MGI:3772798	F	MP:0001884	mammary gland alveolar hyperplasia	Etv6<tm3(NTRK3)Sho>/Etv6<+>,Tg(Wap-cre)11738Mam/0	involves: 129S1/Sv * C57BL/6 * SJL	N	18068631
MGI:3772877	F	MP:0001672	abnormal embryo development	Tsix/Xist<tm3Sado>/Tsix<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	18057104
MGI:3772877	F	MP:0008877	abnormal DNA methylation	Tsix/Xist<tm3Sado>/Tsix<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	18057104
MGI:3772877	F	MP:0011110	preweaning lethality, incomplete penetrance	Tsix/Xist<tm3Sado>/Tsix<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	18057104
MGI:3772878	F	MP:0001672	abnormal embryo development	Tsix/Xist<tm3Sado>/Xist<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	18057104
MGI:3772878	F	MP:0008877	abnormal DNA methylation	Tsix/Xist<tm3Sado>/Xist<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	18057104
MGI:3772878	F	MP:0011110	preweaning lethality, incomplete penetrance	Tsix/Xist<tm3Sado>/Xist<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	18057104
MGI:3772879	F	MP:0011091	prenatal lethality, complete penetrance	Xist<tm4Sado>/Xist<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	18057104
MGI:3772880	M	MP:0011091	prenatal lethality, complete penetrance	Xist<tm4Sado>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	18057104
MGI:3772891	F	MP:0005384	cellular phenotype	Tsix<tm1Jtl>/Tsix<tm1Jtl>	involves: 129S4/SvJae	Y	10520993
MGI:3772894	F	MP:0003787	abnormal imprinting	Xist<tm1Nbd>/Xist<tm1Nbd>	involves: 129 * C57BL/6	N	11230177
MGI:3772895	F	MP:0002169	no abnormal phenotype detected	Xist<tm1Jae>/Xist<tm2Jae>	involves: 129S4/SvJae	N	10431231
MGI:3772897	F	MP:0002169	no abnormal phenotype detected	Xist<tm1Jae>/Xist<tm2.1Jae>	involves: 129S4/SvJae	N	10431231
MGI:3773443	M	MP:0002169	no abnormal phenotype detected	Ar<tm1Chc>/Y	involves: 129S/SvEv * C57BL/6J	N	12370412
MGI:3773444	M	MP:0009285	increased gonadal fat pad weight	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0002780	decreased circulating testosterone level	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0005559	increased circulating glucose level	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0006379	abnormal spermatocyte morphology	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	17142319
MGI:3773444	M	MP:0009115	abnormal fat cell morphology	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0009199	abnormal external male genitalia morphology	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0001155	arrest of spermatogenesis	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0003205	testicular atrophy	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0001262	decreased body weight	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0002780	decreased circulating testosterone level	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0003124	hypospadia	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0002784	abnormal Sertoli cell morphology	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	17142319
MGI:3773444	M	MP:0002784	abnormal Sertoli cell morphology	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0009355	increased liver triglyceride level	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0001552	increased circulating triglyceride level	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0003642	absent seminal vesicle	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0004984	increased osteoclast cell number	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0002079	increased circulating insulin level	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0005293	impaired glucose tolerance	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0003557	absent vas deferens	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0000130	abnormal trabecular bone morphology	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0009115	abnormal fat cell morphology	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0002669	abnormal scrotum morphology	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0013598	Leydig cell hypertrophy	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0001159	absent prostate gland	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0001154	seminiferous tubule degeneration	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	17142319
MGI:3773444	M	MP:0014441	decreased response to leptin	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0000008	increased white adipose tissue amount	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0001147	small testis	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	17142319
MGI:3773444	M	MP:0005331	insulin resistance	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0004893	decreased adiponectin level	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0002216	abnormal seminiferous tubule morphology	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	17142319
MGI:3773444	M	MP:0009204	absent external male genitalia	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0001559	hyperglycemia	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0009302	increased renal fat pad weight	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0001153	small seminiferous tubules	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	17142319
MGI:3773444	M	MP:0031415	increased skeletal muscle triglyceride level	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0000133	abnormal long bone metaphysis morphology	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0008261	arrest of male meiosis	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	17142319
MGI:3773444	M	MP:0004727	absent epididymis	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0001262	decreased body weight	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0020039	increased bone ossification	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0002780	decreased circulating testosterone level	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	17142319
MGI:3773444	M	MP:0002286	cryptorchism	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0005189	abnormal anogenital distance	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0006378	abnormal spermatogonia morphology	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0002286	cryptorchism	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	17142319
MGI:3773444	M	MP:0001940	testis hypoplasia	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773444	M	MP:0005455	increased susceptibility to weight gain	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0005669	increased circulating leptin level	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	15919793
MGI:3773444	M	MP:0005188	small penis	Ar<tm1Chc>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773445	F	MP:0001935	decreased litter size	Ar<tm1Chc>/Ar<+>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773446	F	MP:0000709	enlarged thymus	Ar<tm1Chc>/Ar<tm1.1Chc>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	14676301
MGI:3773446	F	MP:0001935	decreased litter size	Ar<tm1Chc>/Ar<tm1.1Chc>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	12370412
MGI:3773446	F	MP:0001382	abnormal nursing	Ar<tm1Chc>/Ar<tm1.1Chc>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	14676301
MGI:3773446	F	MP:0000627	abnormal mammary gland morphology	Ar<tm1Chc>/Ar<tm1.1Chc>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	14676301
MGI:3773446	F	MP:0004905	decreased uterus weight	Ar<tm1Chc>/Ar<tm1.1Chc>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	14676301
MGI:3773446	F	MP:0004856	decreased ovary weight	Ar<tm1Chc>/Ar<tm1.1Chc>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	14676301
MGI:3773446	F	MP:0000662	abnormal branching of the mammary ductal tree	Ar<tm1Chc>/Ar<tm1.1Chc>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	14676301
MGI:3773446	F	MP:0001882	abnormal lactation	Ar<tm1Chc>/Ar<tm1.1Chc>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	14676301
MGI:3773446	F	MP:0009066	decreased oviduct weight	Ar<tm1Chc>/Ar<tm1.1Chc>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S/SvEv * C57BL/6J * FVB/N	N	14676301
MGI:3773622	M	MP:0001925	male infertility	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	15107499
MGI:3773622	M	MP:0001930	abnormal meiosis	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	17142319
MGI:3773622	M	MP:0004852	decreased testis weight	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	15107499
MGI:3773622	M	MP:0008261	arrest of male meiosis	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	15107499
MGI:3773622	M	MP:0001147	small testis	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	17142319
MGI:3773622	M	MP:0001925	male infertility	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	17142319
MGI:3773622	M	MP:0001156	abnormal spermatogenesis	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	15107499
MGI:3773622	M	MP:0005159	azoospermia	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	15107499
MGI:3773622	M	MP:0002216	abnormal seminiferous tubule morphology	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	15107499
MGI:3773622	M	MP:0002780	decreased circulating testosterone level	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	17142319
MGI:3773622	M	MP:0002780	decreased circulating testosterone level	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	15107499
MGI:3773622	M	MP:0005159	azoospermia	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	17142319
MGI:3773622	M	MP:0004901	decreased male germ cell number	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	15107499
MGI:3773622	M	MP:0002216	abnormal seminiferous tubule morphology	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	17142319
MGI:3773622	M	MP:0001750	increased circulating follicle stimulating hormone level	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	15107499
MGI:3773622	M	MP:0001751	increased circulating luteinizing hormone level	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	15107499
MGI:3773622	M	MP:0008261	arrest of male meiosis	Ar<tm1Chc>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S/SvEv * C57BL/6 * SJL	N	17142319
MGI:3773633	M	MP:0003642	absent seminal vesicle	Ar<tm1.1Chc>/Y	involves: 129S/SvEv * C57BL/6 * FVB/N	N	15107499
MGI:3773633	M	MP:0001155	arrest of spermatogenesis	Ar<tm1.1Chc>/Y	involves: 129S/SvEv * C57BL/6 * FVB/N	N	15107499
MGI:3773633	M	MP:0002009	preneoplasia	Ar<tm1.1Chc>/Y	involves: 129S/SvEv * C57BL/6 * FVB/N	N	17406000
MGI:3773633	M	MP:0001147	small testis	Ar<tm1.1Chc>/Y	involves: 129S/SvEv * C57BL/6 * FVB/N	N	15107499
MGI:3773633	M	MP:0002780	decreased circulating testosterone level	Ar<tm1.1Chc>/Y	involves: 129S/SvEv * C57BL/6 * FVB/N	N	15107499
MGI:3773633	M	MP:0004727	absent epididymis	Ar<tm1.1Chc>/Y	involves: 129S/SvEv * C57BL/6 * FVB/N	N	15107499
MGI:3773633	M	MP:0004502	decreased incidence of tumors by chemical induction	Ar<tm1.1Chc>/Y	involves: 129S/SvEv * C57BL/6 * FVB/N	N	17406000
MGI:3773633	M	MP:0003448	abnormal tumor morphology	Ar<tm1.1Chc>/Y	involves: 129S/SvEv * C57BL/6 * FVB/N	N	17406000
MGI:3773633	M	MP:0001159	absent prostate gland	Ar<tm1.1Chc>/Y	involves: 129S/SvEv * C57BL/6 * FVB/N	N	15107499
MGI:3773633	M	MP:0001751	increased circulating luteinizing hormone level	Ar<tm1.1Chc>/Y	involves: 129S/SvEv * C57BL/6 * FVB/N	N	15107499
MGI:3773634	M	MP:0005389	reproductive system phenotype	Ar<tm1Chc>/Y,Tg(Pbsn-cre)4Prb/0	involves: 129S/SvEv * C57BL/6 * DBA/2	Y	17652515
MGI:3773634	M	MP:0001168	abnormal prostate gland epithelium morphology	Ar<tm1Chc>/Y,Tg(Pbsn-cre)4Prb/0	involves: 129S/SvEv * C57BL/6 * DBA/2	N	17652515
MGI:3773634	M	MP:0001158	abnormal prostate gland morphology	Ar<tm1Chc>/Y,Tg(Pbsn-cre)4Prb/0	involves: 129S/SvEv * C57BL/6 * DBA/2	N	17652515
MGI:3773634	M	MP:0005376	homeostasis/metabolism phenotype	Ar<tm1Chc>/Y,Tg(Pbsn-cre)4Prb/0	involves: 129S/SvEv * C57BL/6 * DBA/2	Y	17652515
MGI:3773634	M	MP:0031357	enlarged prostate gland ventral lobe	Ar<tm1Chc>/Y,Tg(Pbsn-cre)4Prb/0	involves: 129S/SvEv * C57BL/6 * DBA/2	N	17652515
MGI:3773725	F	MP:0001119	abnormal female reproductive system morphology	sho/sho	Not Specified	N	13893329
MGI:3773725	F	MP:0011727	ectopic ovary	sho/sho	Not Specified	N	13893329
MGI:3773725	F	MP:0003574	abnormal oviduct morphology	sho/sho	Not Specified	N	13893329
MGI:3773757	F	MP:0000630	mammary gland hyperplasia	Tg(Wnt1)1Hev/0	involves: C57BL/6 * FVB * SJL	N	15601467
MGI:3773757	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(Wnt1)1Hev/0	involves: C57BL/6 * FVB * SJL	N	15601467
MGI:3773758	F	MP:0000662	abnormal branching of the mammary ductal tree	Id2<tm1Yyk>/Id2<tm1Yyk>,Tg(Wnt1)1Hev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB * SJL	N	15601467
MGI:3773758	F	MP:0000630	mammary gland hyperplasia	Id2<tm1Yyk>/Id2<tm1Yyk>,Tg(Wnt1)1Hev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB * SJL	N	15601467
MGI:3773817	F	MP:0000630	mammary gland hyperplasia	Id2<tm1Yyk>/Id2<+>,Tg(Wnt1)1Hev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB * SJL	N	15601467
MGI:3773817	F	MP:0000662	abnormal branching of the mammary ductal tree	Id2<tm1Yyk>/Id2<+>,Tg(Wnt1)1Hev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB * SJL	N	15601467
MGI:3774843	F	MP:0001560	abnormal circulating insulin level	Lepr<db>/Lepr<+>	involves: C57BLKS/J	N	11416008
MGI:3774843	F	MP:0003953	abnormal hormone level	Lepr<db>/Lepr<+>	involves: C57BLKS/J	N	11416008
MGI:3774843	F	MP:0005559	increased circulating glucose level	Lepr<db>/Lepr<+>	involves: C57BLKS/J	N	11416008
MGI:3774843	F	MP:0005455	increased susceptibility to weight gain	Lepr<db>/Lepr<+>	involves: C57BLKS/J	N	11416008
MGI:3774843	F	MP:0011939	increased food intake	Lepr<db>/Lepr<+>	involves: C57BLKS/J	N	11416008
MGI:3774843	F	MP:0010024	increased total body fat amount	Lepr<db>/Lepr<+>	involves: C57BLKS/J	N	11416008
MGI:3774843	F	MP:0002727	decreased circulating insulin level	Lepr<db>/Lepr<+>	involves: C57BLKS/J	N	25353183
MGI:3774860	F	MP:0004868	increased endometrial carcinoma incidence	Stk11<tm1.2Rdp>/Stk11<+>	involves: 129S6/SvEvTac * FVB/N	N	18245476
MGI:3774861	F	MP:0004868	increased endometrial carcinoma incidence	Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>	involves: 129S6/SvEvTac * FVB/N	N	18245476
MGI:3775036	M	MP:0005389	reproductive system phenotype	Ar<tm1Chc>/Y,Tg(Sycp1-cre)4Min/0	involves: 129S/SvEv * C57BL/6 * DBA/2	Y	17142319
MGI:3775037	M	MP:0001930	abnormal meiosis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ar<tm1Chc>/Y	involves: 129S/SvEv * C57BL/6	N	17142319
MGI:3775037	M	MP:0001925	male infertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ar<tm1Chc>/Y	involves: 129S/SvEv * C57BL/6	N	17142319
MGI:3775037	M	MP:0002780	decreased circulating testosterone level	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ar<tm1Chc>/Y	involves: 129S/SvEv * C57BL/6	N	17142319
MGI:3775037	M	MP:0001153	small seminiferous tubules	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ar<tm1Chc>/Y	involves: 129S/SvEv * C57BL/6	N	17142319
MGI:3775037	M	MP:0001147	small testis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ar<tm1Chc>/Y	involves: 129S/SvEv * C57BL/6	N	17142319
MGI:3775037	M	MP:0005159	azoospermia	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ar<tm1Chc>/Y	involves: 129S/SvEv * C57BL/6	N	17142319
MGI:3775037	M	MP:0008261	arrest of male meiosis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ar<tm1Chc>/Y	involves: 129S/SvEv * C57BL/6	N	17142319
MGI:3775037	M	MP:0002216	abnormal seminiferous tubule morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ar<tm1Chc>/Y	involves: 129S/SvEv * C57BL/6	N	17142319
MGI:3775037	M	MP:0001155	arrest of spermatogenesis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ar<tm1Chc>/Y	involves: 129S/SvEv * C57BL/6	N	17142319
MGI:3775038	F	MP:0002009	preneoplasia	Ar<tm1.1Chc>/Ar<tm1.1Chc>	involves: 129S/SvEv * C57BL/6 * FVB/N	N	17406000
MGI:3775038	F	MP:0004502	decreased incidence of tumors by chemical induction	Ar<tm1.1Chc>/Ar<tm1.1Chc>	involves: 129S/SvEv * C57BL/6 * FVB/N	N	17406000
MGI:3775086	M	MP:0030484	abnormal osteocyte lacuna morphology	Phex<tm1.1Mkd>/Y,Tg(BGLAP-cre)1Clem/0	B6.Cg-Phex<tm1.1Mkd> Tg(BGLAP-cre)1Clem	N	18172553
MGI:3775086	M	MP:0003109	short femur	Phex<tm1.1Mkd>/Y,Tg(BGLAP-cre)1Clem/0	B6.Cg-Phex<tm1.1Mkd> Tg(BGLAP-cre)1Clem	N	18172553
MGI:3775086	M	MP:0000198	decreased circulating phosphate level	Phex<tm1.1Mkd>/Y,Tg(BGLAP-cre)1Clem/0	B6.Cg-Phex<tm1.1Mkd> Tg(BGLAP-cre)1Clem	N	18172553
MGI:3775086	M	MP:0030485	abnormal osteocyte lacunocanalicular system morphology	Phex<tm1.1Mkd>/Y,Tg(BGLAP-cre)1Clem/0	B6.Cg-Phex<tm1.1Mkd> Tg(BGLAP-cre)1Clem	N	18172553
MGI:3775086	M	MP:0009445	osteomalacia	Phex<tm1.1Mkd>/Y,Tg(BGLAP-cre)1Clem/0	B6.Cg-Phex<tm1.1Mkd> Tg(BGLAP-cre)1Clem	N	18172553
MGI:3775086	M	MP:0010110	abnormal renal phosphate reabsorption	Phex<tm1.1Mkd>/Y,Tg(BGLAP-cre)1Clem/0	B6.Cg-Phex<tm1.1Mkd> Tg(BGLAP-cre)1Clem	N	18172553
MGI:3775086	M	MP:0004686	decreased length of long bones	Phex<tm1.1Mkd>/Y,Tg(BGLAP-cre)1Clem/0	B6.Cg-Phex<tm1.1Mkd> Tg(BGLAP-cre)1Clem	N	18172553
MGI:3775087	M	MP:0004686	decreased length of long bones	Phex<tm1.2Mkd>/Y	B6.129-Phex<tm1.2Mkd>	N	18172553
MGI:3775087	M	MP:0030485	abnormal osteocyte lacunocanalicular system morphology	Phex<tm1.2Mkd>/Y	B6.129-Phex<tm1.2Mkd>	N	18172553
MGI:3775087	M	MP:0000198	decreased circulating phosphate level	Phex<tm1.2Mkd>/Y	B6.129-Phex<tm1.2Mkd>	N	18172553
MGI:3775087	M	MP:0010110	abnormal renal phosphate reabsorption	Phex<tm1.2Mkd>/Y	B6.129-Phex<tm1.2Mkd>	N	18172553
MGI:3775087	M	MP:0003109	short femur	Phex<tm1.2Mkd>/Y	B6.129-Phex<tm1.2Mkd>	N	18172553
MGI:3775087	M	MP:0009445	osteomalacia	Phex<tm1.2Mkd>/Y	B6.129-Phex<tm1.2Mkd>	N	18172553
MGI:3775087	M	MP:0030484	abnormal osteocyte lacuna morphology	Phex<tm1.2Mkd>/Y	B6.129-Phex<tm1.2Mkd>	N	18172553
MGI:3775305	F	MP:0001293	anophthalmia	Apln<tm1Ntak>/Apln<tm1Ntak>	involves: 129X1/SvJ * C57BL/6J	N	18200044
MGI:3775305	F	MP:0005380	embryo phenotype	Apln<tm1Ntak>/Apln<tm1Ntak>	involves: 129X1/SvJ * C57BL/6J	Y	18200044
MGI:3775305	F	MP:0020329	decreased capillary density	Apln<tm1Ntak>/Apln<tm1Ntak>	involves: 129X1/SvJ * C57BL/6J	N	18200044
MGI:3775305	F	MP:0005412	vascular stenosis	Apln<tm1Ntak>/Apln<tm1Ntak>	involves: 129X1/SvJ * C57BL/6J	N	18200044
MGI:3775305	F	MP:0001263	weight loss	Apln<tm1Ntak>/Apln<tm1Ntak>	involves: 129X1/SvJ * C57BL/6J	N	18200044
MGI:3775306	F	MP:0003658	abnormal capillary morphology	Apln<tm1Ntak>/Apln<tm1Ntak>,Tg(KRT14-Angpt1)1Gdy/0	involves: 129X1/SvJ * C57BL/6J	N	18200044
MGI:3775407	F	MP:0005044	sepsis	Cfp<tm1Cmst>/Cfp<tm1Cmst>	B6.129P2-Cfp<tm1Cmst>	N	18292556
MGI:3775407	F	MP:0009763	increased susceptibility to induced morbidity/mortality	Cfp<tm1Cmst>/Cfp<tm1Cmst>	B6.129P2-Cfp<tm1Cmst>	N	18292556
MGI:3775439	F	MP:0001806	decreased IgM level	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	18212118
MGI:3775439	F	MP:0008498	decreased IgG3 level	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	18212118
MGI:3775439	F	MP:0002492	decreased IgE level	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	18212118
MGI:3775439	F	MP:0008497	decreased IgG2b level	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	18212118
MGI:3775439	F	MP:0008496	decreased IgG2a level	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	18212118
MGI:3775439	F	MP:0008040	decreased NK T cell number	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	18212118
MGI:3775439	F	MP:0008495	decreased IgG1 level	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	18212118
MGI:3775439	F	MP:0008178	decreased germinal center B cell number	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Cd4-cre)1Cwi/0	involves: C57BL/6 * DBA/2	N	18212118
MGI:3775440	F	MP:0002492	decreased IgE level	Sh2d1a<tm2.1Vei>/Sh2d1a<tm2.1Vei>	involves: C57BL/6	N	18212118
MGI:3775440	F	MP:0001806	decreased IgM level	Sh2d1a<tm2.1Vei>/Sh2d1a<tm2.1Vei>	involves: C57BL/6	N	18212118
MGI:3775440	F	MP:0008178	decreased germinal center B cell number	Sh2d1a<tm2.1Vei>/Sh2d1a<tm2.1Vei>	involves: C57BL/6	N	18212118
MGI:3775440	F	MP:0008497	decreased IgG2b level	Sh2d1a<tm2.1Vei>/Sh2d1a<tm2.1Vei>	involves: C57BL/6	N	18212118
MGI:3775440	F	MP:0008495	decreased IgG1 level	Sh2d1a<tm2.1Vei>/Sh2d1a<tm2.1Vei>	involves: C57BL/6	N	18212118
MGI:3775440	F	MP:0008496	decreased IgG2a level	Sh2d1a<tm2.1Vei>/Sh2d1a<tm2.1Vei>	involves: C57BL/6	N	18212118
MGI:3775440	F	MP:0008040	decreased NK T cell number	Sh2d1a<tm2.1Vei>/Sh2d1a<tm2.1Vei>	involves: C57BL/6	N	18212118
MGI:3775440	F	MP:0008498	decreased IgG3 level	Sh2d1a<tm2.1Vei>/Sh2d1a<tm2.1Vei>	involves: C57BL/6	N	18212118
MGI:3775441	F	MP:0002492	decreased IgE level	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Lck-cre)1Cwi/0	involves: C57BL/6	N	18212118
MGI:3775441	F	MP:0008498	decreased IgG3 level	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Lck-cre)1Cwi/0	involves: C57BL/6	N	18212118
MGI:3775441	F	MP:0008497	decreased IgG2b level	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Lck-cre)1Cwi/0	involves: C57BL/6	N	18212118
MGI:3775441	F	MP:0008040	decreased NK T cell number	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Lck-cre)1Cwi/0	involves: C57BL/6	N	18212118
MGI:3775441	F	MP:0001806	decreased IgM level	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Lck-cre)1Cwi/0	involves: C57BL/6	N	18212118
MGI:3775441	F	MP:0008496	decreased IgG2a level	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Lck-cre)1Cwi/0	involves: C57BL/6	N	18212118
MGI:3775441	F	MP:0008495	decreased IgG1 level	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Lck-cre)1Cwi/0	involves: C57BL/6	N	18212118
MGI:3775441	F	MP:0008178	decreased germinal center B cell number	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Tg(Lck-cre)1Cwi/0	involves: C57BL/6	N	18212118
MGI:3775442	F	MP:0005387	immune system phenotype	Sh2d1a<tm2Vei>/Sh2d1a<tm2Vei>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	Y	18212118
MGI:3775499	F	MP:0004179	transmission ratio distortion	Cftr<tm1Unc>/Cftr<+>,Tmrdq1<BALB/cJ>/Tmrdq1<BALB/cJ>	involves: BALB/cJ * C57BL/6J	N	17506901
MGI:3776121	F	MP:0001923	reduced female fertility	Agtpbp1<pcd-8J>/Agtpbp1<pcd-8J>	BALB/cJ-Agtpbp1<pcd-8J>/GrsrJ	N	MGI:3776074
MGI:3776121	M	MP:0001925	male infertility	Agtpbp1<pcd-8J>/Agtpbp1<pcd-8J>	BALB/cJ-Agtpbp1<pcd-8J>/GrsrJ	N	MGI:3776074
MGI:3776121	M	MP:0006362	abnormal male germ cell morphology	Agtpbp1<pcd-8J>/Agtpbp1<pcd-8J>	BALB/cJ-Agtpbp1<pcd-8J>/GrsrJ	N	MGI:3776074
MGI:3776236	F	MP:0001386	abnormal maternal nurturing	Shank1<tm1Shng>/Shank1<tm1Shng>	involves: 129S4/SvJae * C57BL/6	N	18272690
MGI:3776413	M	MP:0001925	male infertility	Eya4<tm1Jse>/Eya4<tm1Jse>	involves: 129S6/SvEvTac * CBA/J	N	18219393
MGI:3776480	M	MP:0008071	absent B cells	Il2rg<tm1Cgn>/Y,Rag2<tm1Fwa>/Rag2<tm1Fwa>	B6.129-Rag2<tm1Fwa> Il2rg<tm1Cgn>	N	12586624
MGI:3776480	M	MP:0008070	absent T cells	Il2rg<tm1Cgn>/Y,Rag2<tm1Fwa>/Rag2<tm1Fwa>	B6.129-Rag2<tm1Fwa> Il2rg<tm1Cgn>	N	12586624
MGI:3776480	M	MP:0008046	absent NK cells	Il2rg<tm1Cgn>/Y,Rag2<tm1Fwa>/Rag2<tm1Fwa>	B6.129-Rag2<tm1Fwa> Il2rg<tm1Cgn>	N	12586624
MGI:3776484	M	MP:0008045	decreased NK cell number	Il2rg<tm2Cgn>/Y,Tg(Mx1-cre)1Cgn/?	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	12586624
MGI:3776560	M	MP:0011642	abnormal bone collagen fibril morphology	Col1a1<m1Btlr>/Col1a1<m1Btlr>	C57BL/6J-Col1a1<m1Btlr>	N	28916811
MGI:3776560	M	MP:0000558	abnormal tibia morphology	Col1a1<m1Btlr>/Col1a1<m1Btlr>	C57BL/6J-Col1a1<m1Btlr>	N	28916811
MGI:3776560	M	MP:0001262	decreased body weight	Col1a1<m1Btlr>/Col1a1<m1Btlr>	C57BL/6J-Col1a1<m1Btlr>	N	28916811
MGI:3776560	M	MP:0000135	decreased compact bone thickness	Col1a1<m1Btlr>/Col1a1<m1Btlr>	C57BL/6J-Col1a1<m1Btlr>	N	28916811
MGI:3776560	M	MP:0030679	decreased hydroxyproline level	Col1a1<m1Btlr>/Col1a1<m1Btlr>	C57BL/6J-Col1a1<m1Btlr>	N	28916811
MGI:3776560	M	MP:0000130	abnormal trabecular bone morphology	Col1a1<m1Btlr>/Col1a1<m1Btlr>	C57BL/6J-Col1a1<m1Btlr>	N	28916811
MGI:3776560	M	MP:0000755	hindlimb paralysis	Col1a1<m1Btlr>/Col1a1<m1Btlr>	C57BL/6J-Col1a1<m1Btlr>	N	28916811
MGI:3776560	M	MP:0000547	short limbs	Col1a1<m1Btlr>/Col1a1<m1Btlr>	C57BL/6J-Col1a1<m1Btlr>	N	28916811
MGI:3776560	M	MP:0001392	abnormal locomotor behavior	Col1a1<m1Btlr>/Col1a1<m1Btlr>	C57BL/6J-Col1a1<m1Btlr>	N	28916811
MGI:3776560	M	MP:0004686	decreased length of long bones	Col1a1<m1Btlr>/Col1a1<m1Btlr>	C57BL/6J-Col1a1<m1Btlr>	N	28916811
MGI:3776560	M	MP:0000572	abnormal autopod morphology	Col1a1<m1Btlr>/Col1a1<m1Btlr>	C57BL/6J-Col1a1<m1Btlr>	N	28916811
MGI:3776560	M	MP:0000559	abnormal femur morphology	Col1a1<m1Btlr>/Col1a1<m1Btlr>	C57BL/6J-Col1a1<m1Btlr>	N	28916811
MGI:3776560	M	MP:0000061	fragile skeleton	Col1a1<m1Btlr>/Col1a1<m1Btlr>	C57BL/6J-Col1a1<m1Btlr>	N	28916811
MGI:3776781	M	MP:0008261	arrest of male meiosis	Del(MTmt-Tk-mt-Nd5)1Jiha	involves: C57BL/6J * CBA	N	17005726
MGI:3776781	M	MP:0009831	abnormal sperm midpiece morphology	Del(MTmt-Tk-mt-Nd5)1Jiha	involves: C57BL/6J * CBA	N	17005726
MGI:3776781	M	MP:0005578	teratozoospermia	Del(MTmt-Tk-mt-Nd5)1Jiha	involves: C57BL/6J * CBA	N	17005726
MGI:3776781	M	MP:0009232	abnormal sperm nucleus morphology	Del(MTmt-Tk-mt-Nd5)1Jiha	involves: C57BL/6J * CBA	N	17005726
MGI:3776781	M	MP:0001380	reduced male mating frequency	Del(MTmt-Tk-mt-Nd5)1Jiha	involves: C57BL/6J * CBA	N	17005726
MGI:3776781	M	MP:0002675	asthenozoospermia	Del(MTmt-Tk-mt-Nd5)1Jiha	involves: C57BL/6J * CBA	N	17005726
MGI:3776781	M	MP:0002687	oligozoospermia	Del(MTmt-Tk-mt-Nd5)1Jiha	involves: C57BL/6J * CBA	N	17005726
MGI:3776781	M	MP:0001925	male infertility	Del(MTmt-Tk-mt-Nd5)1Jiha	involves: C57BL/6J * CBA	N	17005726
MGI:3776781	M	MP:0009234	absent sperm head	Del(MTmt-Tk-mt-Nd5)1Jiha	involves: C57BL/6J * CBA	N	17005726
MGI:3776840	F	MP:0001926	female infertility	Tcf3<tm1Zhu>/Tcf3<tm1Zhu>	involves: 129	N	9584174
MGI:3776843	F	MP:0001926	female infertility	Tcf3<tm2Wein>/Tcf3<tm2Wein>	Not Specified	N	9584174
MGI:3776844	F	MP:0001926	female infertility	Tcf3<tm1Wein>/Tcf3<tm1Wein>	involves: 129S4/SvJaeSor	N	9584174
MGI:3776851	M	MP:0001156	abnormal spermatogenesis	Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd	N	18232736
MGI:3776851	M	MP:0001925	male infertility	Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd	N	18232736
MGI:3776851	M	MP:0006362	abnormal male germ cell morphology	Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd	N	18232736
MGI:3776851	M	MP:0006378	abnormal spermatogonia morphology	Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd	N	18232736
MGI:3776851	F	MP:0001926	female infertility	Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd	N	18232736
MGI:3776851	M	MP:0006379	abnormal spermatocyte morphology	Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd	N	18232736
MGI:3776851	M	MP:0001147	small testis	Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd	N	18232736
MGI:3776851	M	MP:0006380	abnormal spermatid morphology	Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd	N	18232736
MGI:3777244	M	MP:0001925	male infertility	Lfng<tm1Rjo>/Lfng<tm1Rjo>	either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * FVB/N)	N	18234727
MGI:3777292	M	MP:0009235	small sperm head	Wipf3<tm1Tta>/Wipf3<tm1Tta>	involves: 129P2/OlaHsd * C57BL/6J	N	17573773
MGI:3777292	M	MP:0005578	teratozoospermia	Wipf3<tm1Tta>/Wipf3<tm1Tta>	involves: 129P2/OlaHsd * C57BL/6J	N	17573773
MGI:3777292	M	MP:0001922	reduced male fertility	Wipf3<tm1Tta>/Wipf3<tm1Tta>	involves: 129P2/OlaHsd * C57BL/6J	N	17573773
MGI:3777292	M	MP:0009230	abnormal sperm head morphology	Wipf3<tm1Tta>/Wipf3<tm1Tta>	involves: 129P2/OlaHsd * C57BL/6J	N	17573773
MGI:3777292	M	MP:0006380	abnormal spermatid morphology	Wipf3<tm1Tta>/Wipf3<tm1Tta>	involves: 129P2/OlaHsd * C57BL/6J	N	17573773
MGI:3777292	M	MP:0001156	abnormal spermatogenesis	Wipf3<tm1Tta>/Wipf3<tm1Tta>	involves: 129P2/OlaHsd * C57BL/6J	N	17573773
MGI:3777383	M	MP:0001922	reduced male fertility	Pla2g6<tm1Tsu>/Pla2g6<tm1Tsu>	involves: 129S2/SvPas * C57BL/6	N	18305254
MGI:3777915	F	MP:0010389	mosaic coat color	Atp7a<Mo-Btlr>/Atp7a<+>	C57BL/6J-Atp7a<Mo-Btlr>	N	MGI:3777742
MGI:3777915	F	MP:0010389	mosaic coat color	Atp7a<Mo-Btlr>/Atp7a<+>	C57BL/6J-Atp7a<Mo-Btlr>	N	22869751
MGI:3777916	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-Btlr>/Y	C57BL/6J-Atp7a<Mo-Btlr>	N	22869751
MGI:3777916	M	MP:0011089	perinatal lethality, complete penetrance	Atp7a<Mo-Btlr>/Y	C57BL/6J-Atp7a<Mo-Btlr>	N	MGI:3777742
MGI:3777944	F	MP:0001926	female infertility	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	M	MP:0001147	small testis	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	F	MP:0005431	decreased oocyte number	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	M	MP:0001153	small seminiferous tubules	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	F	MP:0009363	abnormal tertiary ovarian follicle morphology	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	M	MP:0003205	testicular atrophy	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	F	MP:0009375	thin zona pellucida	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	F	MP:0004856	decreased ovary weight	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	F	MP:0005168	abnormal female meiosis	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	F	MP:0001125	abnormal oocyte morphology	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	F	MP:0002682	decreased mature ovarian follicle number	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	F	MP:0031422	failure of superovulation	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	M	MP:0013600	testis degeneration	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	F	MP:0001127	small ovary	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	M	MP:0001925	male infertility	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	M	MP:0004901	decreased male germ cell number	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	F	MP:0002680	decreased corpora lutea number	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	M	MP:0008261	arrest of male meiosis	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3777944	F	MP:0014447	impaired spindle assembly in female meiosis	Ubb<tm1Rrk>/Ubb<tm1Rrk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18070917
MGI:3778161	F	MP:0002169	no abnormal phenotype detected	Dkc1<tm1Bsl>/Dkc1<tm1Bsl>	involves: 129/Sv * C57BL/6	N	12400016
MGI:3778162	M	MP:0002169	no abnormal phenotype detected	Dkc1<tm1Bsl>/Y	involves: 129/Sv * C57BL/6	N	12400016
MGI:3778163	F	MP:0002169	no abnormal phenotype detected	Dkc1<tm2Bsl>/Dkc1<tm2Bsl>	involves: 129/Sv * C57BL/6	N	12400016
MGI:3778164	M	MP:0002169	no abnormal phenotype detected	Dkc1<tm2Bsl>/Y	involves: 129/Sv * C57BL/6	N	12400016
MGI:3778208	M	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance	Dkc1<tm1Bsl>/Y,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778209	M	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance	Dkc1<tm2Bsl>/Y,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778210	F	MP:0001672	abnormal embryo development	Dkc1<tm1Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778210	F	MP:0012119	increased trophectoderm apoptosis	Dkc1<tm1Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778210	F	MP:0004180	failure of initiation of embryo turning	Dkc1<tm1Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778210	F	MP:0004179	transmission ratio distortion	Dkc1<tm1Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778210	F	MP:0001698	decreased embryo size	Dkc1<tm1Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778210	F	MP:0001730	embryonic growth arrest	Dkc1<tm1Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778210	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Dkc1<tm1Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778211	F	MP:0001730	embryonic growth arrest	Dkc1<tm2Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778211	F	MP:0004180	failure of initiation of embryo turning	Dkc1<tm2Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778211	F	MP:0001672	abnormal embryo development	Dkc1<tm2Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778211	F	MP:0004179	transmission ratio distortion	Dkc1<tm2Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778211	F	MP:0012119	increased trophectoderm apoptosis	Dkc1<tm2Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778211	F	MP:0001698	decreased embryo size	Dkc1<tm2Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778211	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Dkc1<tm2Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778212	F	MP:0002169	no abnormal phenotype detected	Dkc1<tm2.1Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778213	F	MP:0002169	no abnormal phenotype detected	Dkc1<tm1.1Bsl>/Dkc1<+>,Tg(Gata1-cre)1Sho/0	involves: 129/Sv * C57BL/6 * CD-1	N	12400016
MGI:3778628	F	MP:0001926	female infertility	Vangl2<Lp>/Vangl2<+>	involves: A	N	20562861
MGI:3778628	F	MP:0001144	vagina atresia	Vangl2<Lp>/Vangl2<+>	involves: A	N	20562861
MGI:3778628	F	MP:0001144	vagina atresia	Vangl2<Lp>/Vangl2<+>	involves: A	N	MGI:61268
MGI:3778813	M	MP:0004852	decreased testis weight	Kit<W-v>/Kit<+>,X/Sry<AKR/J>	involves: AKR/J * C57BL/6J	N	MGI:3778179
MGI:3778814	M	MP:0004852	decreased testis weight	Kit<W-e>/Kit<+>,X/Sry<AKR/J>	involves: AKR/J * C57BL/6J	N	MGI:3778179
MGI:3778815	M	MP:0004852	decreased testis weight	Kit<W-27H>/Kit<+>,X/Sry<AKR/J>	involves: AKR/J * C57BL/6J * CBA/H	N	MGI:3778179
MGI:3778816	M	MP:0004852	decreased testis weight	Del(10)1H/+,X/Sry<AKR/J>	involves: AKR/J * C57BL/6J	N	MGI:3778179
MGI:3778817	M	MP:0004852	decreased testis weight	Kitl<Sl-18H>/Kitl<+>,X/Sry<AKR/J>	involves: AKR/J * C57BL/6J	N	MGI:3778179
MGI:3778818	M	MP:0004852	decreased testis weight	X/Sry<AKR/J>,Tht/Tht<+>	involves: AKR/J * C57BL/6J	N	MGI:3778179
MGI:3778825	F	MP:0001143	constricted vagina orifice	Kit<W-19H>/Kit<+>	B6.Cg-Kit<W-19H>/EiJ	N	MGI:3778531
MGI:3778827	M	MP:0008280	abnormal male germ cell apoptosis	Bax<tm1Sjk>/Bax<+>,Nanos2<tm1Ysa>/Nanos2<tm1Ysa>	involves: 129S1/Sv * 129X1/SvJ	N	18281459
MGI:3778827	M	MP:0005159	azoospermia	Bax<tm1Sjk>/Bax<+>,Nanos2<tm1Ysa>/Nanos2<tm1Ysa>	involves: 129S1/Sv * 129X1/SvJ	N	18281459
MGI:3778828	M	MP:0005159	azoospermia	Bax<tm1Sjk>/Bax<tm1Sjk>,Nanos2<tm1Ysa>/Nanos2<tm1Ysa>	involves: 129S1/Sv * 129X1/SvJ	N	18281459
MGI:3778829	F	MP:0006361	abnormal female germ cell morphology	Nanos3<tm2(cre)Ysa>/Nanos3<+>,Tg(CAG-cat,-Nanos2)1Ysa/0	Not Specified	N	18281459
MGI:3778829	F	MP:0005168	abnormal female meiosis	Nanos3<tm2(cre)Ysa>/Nanos3<+>,Tg(CAG-cat,-Nanos2)1Ysa/0	Not Specified	N	18281459
MGI:3783343	M	MP:0001925	male infertility	Stat3<tm1Flv>/Stat3<tm1Flv>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	15070774
MGI:3783343	F	MP:0001134	absent corpus luteum	Stat3<tm1Flv>/Stat3<tm1Flv>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	15070774
MGI:3783343	F	MP:0009089	short uterine horn	Stat3<tm1Flv>/Stat3<tm1Flv>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	15070774
MGI:3783343	M	MP:0001147	small testis	Stat3<tm1Flv>/Stat3<tm1Flv>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	15070774
MGI:3783343	M	MP:0001157	small seminal vesicle	Stat3<tm1Flv>/Stat3<tm1Flv>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	15070774
MGI:3783343	F	MP:0001926	female infertility	Stat3<tm1Flv>/Stat3<tm1Flv>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	15070774
MGI:3783343	F	MP:0008869	anovulation	Stat3<tm1Flv>/Stat3<tm1Flv>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	15070774
MGI:3783408	M	MP:0006423	dilated rete testis	Car2<n>/Car2<n>	involves: DBA/2J	N	11698654
MGI:3783408	M	MP:0009140	dilated efferent ductule of testis	Car2<n>/Car2<n>	involves: DBA/2J	N	11698654
MGI:3783408	M	MP:0001922	reduced male fertility	Car2<n>/Car2<n>	involves: DBA/2J	N	11698654
MGI:3783421	F	MP:0001926	female infertility	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	18337503
MGI:3783421	M	MP:0008261	arrest of male meiosis	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	18337503
MGI:3783421	M	MP:0001925	male infertility	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	18337503
MGI:3783421	M	MP:0005169	abnormal male meiosis	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	18337503
MGI:3783421	M	MP:0002687	oligozoospermia	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	N	18337503
MGI:3783424	F	MP:0001386	abnormal maternal nurturing	Anxa4<Gt(OST134786)Lex>/Anxa4<Gt(OST134786)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	12912993
MGI:3783471	M	MP:0001925	male infertility	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	M	MP:0005578	teratozoospermia	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	M	MP:0020869	immotile sperm	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	F	MP:0009009	absent estrous cycle	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	M	MP:0006380	abnormal spermatid morphology	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	F	MP:0001127	small ovary	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	M	MP:0002687	oligozoospermia	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	M	MP:0014052	increased male germ cell apoptosis	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	M	MP:0002686	globozoospermia	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	F	MP:0009081	thin uterus	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	F	MP:0001134	absent corpus luteum	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	F	MP:0001927	abnormal estrous cycle	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	F	MP:0008869	anovulation	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	M	MP:0004852	decreased testis weight	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	F	MP:0001382	abnormal nursing	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	F	MP:0001923	reduced female fertility	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783471	M	MP:0008892	abnormal sperm flagellum morphology	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	12482959
MGI:3783532	F	MP:0001923	reduced female fertility	Apaf1<fog>/Apaf1<fog>	involves: C3H/HeJ	N	9216040
MGI:3783532	M	MP:0001922	reduced male fertility	Apaf1<fog>/Apaf1<fog>	involves: C3H/HeJ	N	9216040
MGI:3783586	F	MP:0009873	abnormal aorta tunica media morphology	Cybb<tm1Din>/Cybb<tm1Din>	involves: 129S/SvEv * C57BL/6	N	11349005
MGI:3783586	F	MP:0000511	abnormal intestinal mucosa morphology	Cybb<tm1Din>/Cybb<tm1Din>	involves: 129S/SvEv * C57BL/6	N	10982764
MGI:3783586	F	MP:0002843	decreased systemic arterial blood pressure	Cybb<tm1Din>/Cybb<tm1Din>	involves: 129S/SvEv * C57BL/6	N	11349005
MGI:3783586	F	MP:0001262	decreased body weight	Cybb<tm1Din>/Cybb<tm1Din>	involves: 129S/SvEv * C57BL/6	N	11349005
MGI:3783586	F	MP:0005387	immune system phenotype	Cybb<tm1Din>/Cybb<tm1Din>	involves: 129S/SvEv * C57BL/6	Y	10982764
MGI:3783586	F	MP:0010792	abnormal stomach mucosa morphology	Cybb<tm1Din>/Cybb<tm1Din>	involves: 129S/SvEv * C57BL/6	N	10982764
MGI:3783586	F	MP:0005381	digestive/alimentary phenotype	Cybb<tm1Din>/Cybb<tm1Din>	involves: 129S/SvEv * C57BL/6	Y	10982764
MGI:3783626	F	MP:0008779	abnormal maternal behavior	pn/pn	S-pn	N	MGI:48642
MGI:3783626	F	MP:0002907	abnormal parturition	pn/pn	S-pn	N	MGI:48642
MGI:3783626	F	MP:0001386	abnormal maternal nurturing	pn/pn	S-pn	N	MGI:48642
MGI:3784072	F	MP:0005386	behavior/neurological phenotype	Mcf2<tm1Ehi>/Mcf2<tm1Ehi>	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6	Y	11940671
MGI:3784072	F	MP:0008143	abnormal dendrite morphology	Mcf2<tm1Ehi>/Mcf2<tm1Ehi>	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	11940671
MGI:3784072	F	MP:0003631	nervous system phenotype	Mcf2<tm1Ehi>/Mcf2<tm1Ehi>	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6	Y	11940671
MGI:3784072	F	MP:0005389	reproductive system phenotype	Mcf2<tm1Ehi>/Mcf2<tm1Ehi>	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6	Y	11940671
MGI:3784460	F	MP:0001923	reduced female fertility	Del(6Ephb6-Trpv6)1Mhed/Del(6Ephb6-Trpv6)1Mhed	involves: 129S/SvEv	N	17129178
MGI:3784460	F	MP:0008779	abnormal maternal behavior	Del(6Ephb6-Trpv6)1Mhed/Del(6Ephb6-Trpv6)1Mhed	involves: 129S/SvEv	N	17129178
MGI:3784460	F	MP:0001384	abnormal pup retrieval	Del(6Ephb6-Trpv6)1Mhed/Del(6Ephb6-Trpv6)1Mhed	involves: 129S/SvEv	N	17129178
MGI:3784460	M	MP:0001922	reduced male fertility	Del(6Ephb6-Trpv6)1Mhed/Del(6Ephb6-Trpv6)1Mhed	involves: 129S/SvEv	N	17129178
MGI:3784605	M	MP:0006069	abnormal retina neuronal layer morphology	Morq1<AKR/J>/Morq1<AKR/J>,Rs1<tmgc1>/Y	involves: AKR/J * C3H/Rl * C57BL/6JRn	N	18245825
MGI:3784606	M	MP:0006069	abnormal retina neuronal layer morphology	Morq1<AKR/J>/Morq1<C57BL/6JRn>,Rs1<tmgc1>/Y	involves: AKR/J * C3H/Rl * C57BL/6JRn	N	18245825
MGI:3784607	M	MP:0006069	abnormal retina neuronal layer morphology	Morq1<AKR/J>/Morq1<C3H/Rl>,Rs1<tmgc1>/Y	involves: AKR/J * C3H/Rl * C57BL/6JRn	N	18245825
MGI:3784608	M	MP:0006069	abnormal retina neuronal layer morphology	Morq1<AKR/J>/Morq1<AKR/J>,Rs1<tmgc1>/Y	B6.Cg-Rs1<tmgc1> Morq1<AKR/J>	N	18245825
MGI:3784609	F	MP:0006069	abnormal retina neuronal layer morphology	Morq1<AKR/J>/Morq1<AKR/J>,Rs1<tmgc1>/Rs1<tmgc1>	B6.Cg-Rs1<tmgc1> Morq1<AKR/J>	N	18245825
MGI:3784866	F	MP:0002679	abnormal corpus luteum morphology	Nupr1<tm1Jlio>/Nupr1<tm1Jlio>	involves: 129S1/Sv * 129X1/SvJ	N	18495683
MGI:3784866	F	MP:0001938	delayed sexual maturation	Nupr1<tm1Jlio>/Nupr1<tm1Jlio>	involves: 129S1/Sv * 129X1/SvJ	N	18495683
MGI:3784866	M	MP:0005159	azoospermia	Nupr1<tm1Jlio>/Nupr1<tm1Jlio>	involves: 129S1/Sv * 129X1/SvJ	N	18495683
MGI:3784975	M	MP:0001925	male infertility	Agtpbp1<pcd-Btlr>/Agtpbp1<pcd-Btlr>	C57BL/6J-Agtpbp1<pcd-Btlr>	N	MGI:3778956
MGI:3784975	M	MP:0005578	teratozoospermia	Agtpbp1<pcd-Btlr>/Agtpbp1<pcd-Btlr>	C57BL/6J-Agtpbp1<pcd-Btlr>	N	MGI:3778956
MGI:3784975	M	MP:0002687	oligozoospermia	Agtpbp1<pcd-Btlr>/Agtpbp1<pcd-Btlr>	C57BL/6J-Agtpbp1<pcd-Btlr>	N	MGI:3778956
MGI:3785002	F	MP:0005375	adipose tissue phenotype	Brs3<tm1Jfb>/Brs3<tm1Jfb>	B6.129X1-Brs3<tm1Jfb>	Y	18039774
MGI:3785002	F	MP:0001260	increased body weight	Brs3<tm1Jfb>/Brs3<tm1Jfb>	B6.129X1-Brs3<tm1Jfb>	N	18039774
MGI:3785002	F	MP:0000005	increased brown adipose tissue amount	Brs3<tm1Jfb>/Brs3<tm1Jfb>	B6.129X1-Brs3<tm1Jfb>	N	18039774
MGI:3785002	F	MP:0011939	increased food intake	Brs3<tm1Jfb>/Brs3<tm1Jfb>	B6.129X1-Brs3<tm1Jfb>	N	18039774
MGI:3785002	F	MP:0005449	abnormal food intake	Brs3<tm1Jfb>/Brs3<tm1Jfb>	B6.129X1-Brs3<tm1Jfb>	N	18039774
MGI:3785002	F	MP:0005669	increased circulating leptin level	Brs3<tm1Jfb>/Brs3<tm1Jfb>	B6.129X1-Brs3<tm1Jfb>	N	18039774
MGI:3785002	F	MP:0002079	increased circulating insulin level	Brs3<tm1Jfb>/Brs3<tm1Jfb>	B6.129X1-Brs3<tm1Jfb>	N	18039774
MGI:3785002	F	MP:0000008	increased white adipose tissue amount	Brs3<tm1Jfb>/Brs3<tm1Jfb>	B6.129X1-Brs3<tm1Jfb>	N	18039774
MGI:3785002	F	MP:0006319	abnormal epididymal fat pad morphology	Brs3<tm1Jfb>/Brs3<tm1Jfb>	B6.129X1-Brs3<tm1Jfb>	N	18039774
MGI:3785074	F	MP:0013529	decreased nipple number	Gli3<Xt>/Gli3<Xt>	involves: 101/H * C3H/HeH * CBA/H	N	6049666
MGI:3785074	F	MP:0011727	ectopic ovary	Gli3<Xt>/Gli3<Xt>	involves: 101/H * C3H/HeH * CBA/H	N	6049666
MGI:3785088	F	MP:0000416	sparse hair	Bhrd/Bhrd	B6(V)-Bhrd/GrsrJ	N	MGI:3765079
MGI:3785088	F	MP:0002073	abnormal hair growth	Bhrd/Bhrd	B6(V)-Bhrd/GrsrJ	N	MGI:3765079
MGI:3785287	F	MP:0003699	abnormal female reproductive system physiology	C3<tm1Crr>/C3<tm1Crr>	B6.129S4-C3<tm1Crr>	N	19205046
MGI:3785287	M	MP:0004792	abnormal synaptic vesicle number	C3<tm1Crr>/C3<tm1Crr>	B6.129S4-C3<tm1Crr>	N	26400934
MGI:3785287	F	MP:0009006	prolonged estrous cycle	C3<tm1Crr>/C3<tm1Crr>	B6.129S4-C3<tm1Crr>	N	19205046
MGI:3785287	F	MP:0001729	impaired embryo implantation	C3<tm1Crr>/C3<tm1Crr>	B6.129S4-C3<tm1Crr>	N	19205046
MGI:3785289	F	MP:0002922	decreased post-tetanic potentiation	Cybb<tm1Din>/Cybb<tm1Din>	B6.129S-Cybb<tm1Din>	N	16847341
MGI:3785289	F	MP:0001473	reduced long-term potentiation	Cybb<tm1Din>/Cybb<tm1Din>	B6.129S-Cybb<tm1Din>	N	16847341
MGI:3785289	F	MP:0005387	immune system phenotype	Cybb<tm1Din>/Cybb<tm1Din>	B6.129S-Cybb<tm1Din>	Y	16872848
MGI:3785289	F	MP:0001463	abnormal spatial learning	Cybb<tm1Din>/Cybb<tm1Din>	B6.129S-Cybb<tm1Din>	N	16847341
MGI:3785289	F	MP:0005088	increased acute inflammation	Cybb<tm1Din>/Cybb<tm1Din>	B6.129S-Cybb<tm1Din>	N	16816381
MGI:3785289	F	MP:0002757	decreased vertical activity	Cybb<tm1Din>/Cybb<tm1Din>	B6.129S-Cybb<tm1Din>	N	16847341
MGI:3785289	F	MP:0003447	decreased tumor growth/size	Cybb<tm1Din>/Cybb<tm1Din>	B6.129S-Cybb<tm1Din>	N	16816381
MGI:3785289	F	MP:0002500	granulomatous inflammation	Cybb<tm1Din>/Cybb<tm1Din>	B6.129S-Cybb<tm1Din>	N	19234224
MGI:3785289	F	MP:0001405	impaired coordination	Cybb<tm1Din>/Cybb<tm1Din>	B6.129S-Cybb<tm1Din>	N	16847341
MGI:3785289	F	MP:0001273	decreased metastatic potential	Cybb<tm1Din>/Cybb<tm1Din>	B6.129S-Cybb<tm1Din>	N	16816381
MGI:3785731	F	MP:0005459	decreased percent body fat/body weight	Tg(Pmch-ATXN3*)3Rck/0	involves: FVB/NJ	N	16407534
MGI:3785731	F	MP:0005668	decreased circulating leptin level	Tg(Pmch-ATXN3*)3Rck/0	involves: FVB/NJ	N	16407534
MGI:3785731	M	MP:0005560	decreased circulating glucose level	Tg(Pmch-ATXN3*)3Rck/0	involves: FVB/NJ	N	16407534
MGI:3785731	M	MP:0004889	increased energy expenditure	Tg(Pmch-ATXN3*)3Rck/0	involves: FVB/NJ	N	16407534
MGI:3785731	F	MP:0002727	decreased circulating insulin level	Tg(Pmch-ATXN3*)3Rck/0	involves: FVB/NJ	N	16407534
MGI:3785732	F	MP:0001386	abnormal maternal nurturing	Lep<ob>/Lep<ob>,Tg(Pmch-ATXN3*)3Rck/0	involves: C57BL/6J * FVB/NJ	N	16407534
MGI:3785750	F	MP:0001134	absent corpus luteum	Ddr2<slie>/Ddr2<slie>	BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpe<fat>/LtJng	N	18483174
MGI:3785750	M	MP:0002784	abnormal Sertoli cell morphology	Ddr2<slie>/Ddr2<slie>	BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpe<fat>/LtJng	N	18483174
MGI:3785750	M	MP:0006380	abnormal spermatid morphology	Ddr2<slie>/Ddr2<slie>	BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpe<fat>/LtJng	N	18483174
MGI:3785750	F	MP:0031422	failure of superovulation	Ddr2<slie>/Ddr2<slie>	BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpe<fat>/LtJng	N	18483174
MGI:3785750	F	MP:0001926	female infertility	Ddr2<slie>/Ddr2<slie>	BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpe<fat>/LtJng	N	18483174
MGI:3785750	F	MP:0008869	anovulation	Ddr2<slie>/Ddr2<slie>	BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpe<fat>/LtJng	N	18483174
MGI:3785750	F	MP:0001142	abnormal vagina orifice morphology	Ddr2<slie>/Ddr2<slie>	BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpe<fat>/LtJng	N	18483174
MGI:3785750	M	MP:0006378	abnormal spermatogonia morphology	Ddr2<slie>/Ddr2<slie>	BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpe<fat>/LtJng	N	18483174
MGI:3785750	M	MP:0001922	reduced male fertility	Ddr2<slie>/Ddr2<slie>	BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpe<fat>/LtJng	N	18483174
MGI:3785750	M	MP:0013599	Leydig cell atrophy	Ddr2<slie>/Ddr2<slie>	BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpe<fat>/LtJng	N	18483174
MGI:3785799	M	MP:0004933	abnormal epididymis epithelium morphology	Tg(MMTV-Erbb2)NA1Mul/0	involves: FVB/N	N	2898299
MGI:3785799	M	MP:0001925	male infertility	Tg(MMTV-Erbb2)NA1Mul/0	involves: FVB/N	N	2898299
MGI:3785826	M	MP:0004933	abnormal epididymis epithelium morphology	Tg(MMTV-Erbb2)NF1Mul/0	involves: FVB/N	N	2898299
MGI:3785826	M	MP:0001922	reduced male fertility	Tg(MMTV-Erbb2)NF1Mul/0	involves: FVB/N	N	2898299
MGI:3785826	F	MP:0001382	abnormal nursing	Tg(MMTV-Erbb2)NF1Mul/0	involves: FVB/N	N	2898299
MGI:3785828	M	MP:0001925	male infertility	Tg(MMTV-Erbb2)NB1Mul/0	involves: FVB/N	N	2898299
MGI:3785828	M	MP:0004933	abnormal epididymis epithelium morphology	Tg(MMTV-Erbb2)NB1Mul/0	involves: FVB/N	N	2898299
MGI:3789004	F	MP:0001868	ovary inflammation	Tg(CD2-Ifngr2)2Pbro/?	NOD.Cg-Tg(CD2-Ifngr2)2Pbro	N	12594305
MGI:3789123	M	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0000751	myopathy	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0001405	impaired coordination	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0010106	abnormal circulating pyruvate kinase level	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0008560	increased tumor necrosis factor secretion	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	19451692
MGI:3789123	M	MP:0002269	muscular atrophy	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0002108	abnormal muscle morphology	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0000752	dystrophic muscle	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0008663	increased interleukin-12 secretion	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	19451692
MGI:3789123	M	MP:0008687	increased interleukin-2 secretion	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	19451692
MGI:3789123	M	MP:0008699	increased interleukin-4 secretion	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	19451692
MGI:3789123	M	MP:0009403	increased variability of skeletal muscle fiber size	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0000749	muscle degeneration	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0008566	increased interferon-gamma secretion	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	19451692
MGI:3789123	M	MP:0008705	increased interleukin-6 secretion	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	19451692
MGI:3789123	M	MP:0002066	abnormal motor capabilities/coordination/movement	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0000745	tremors	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0002106	abnormal muscle physiology	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	8433102
MGI:3789123	M	MP:0010090	increased circulating creatine kinase level	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0009419	skeletal muscle fibrosis	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0003852	skeletal muscle necrosis	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789123	M	MP:0004089	dilated sarcoplasmic reticulum	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>/J	N	6583703
MGI:3789135	M	MP:0008752	abnormal tumor necrosis factor level	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9771748
MGI:3789135	M	MP:0005331	insulin resistance	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9771748
MGI:3789135	M	MP:0005658	increased susceptibility to diet-induced obesity	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9771748
MGI:3789135	M	MP:0005293	impaired glucose tolerance	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9771748
MGI:3789135	M	MP:0009302	increased renal fat pad weight	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9771748
MGI:3789135	M	MP:0003212	increased susceptibility to age related obesity	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9771748
MGI:3789135	M	MP:0001559	hyperglycemia	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9771748
MGI:3789135	M	MP:0002079	increased circulating insulin level	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9771748
MGI:3789135	M	MP:0001413	abnormal response to new environment	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9844009
MGI:3789135	M	MP:0000008	increased white adipose tissue amount	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9771748
MGI:3789135	M	MP:0003638	abnormal response/metabolism to endogenous compounds	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9771748
MGI:3789135	M	MP:0001433	polyphagia	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9771748
MGI:3789135	M	MP:0005669	increased circulating leptin level	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9771748
MGI:3789135	M	MP:0001463	abnormal spatial learning	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9844009
MGI:3789135	M	MP:0009288	increased epididymal fat pad weight	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9771748
MGI:3789135	M	MP:0001473	reduced long-term potentiation	Htr2c<tm1Jul>/Y	B6.129S-Htr2c<tm1Jul>	N	9844009
MGI:3789198	F	MP:0004904	increased uterus weight	Apoe<tm1Unc>/Apoe<tm1Unc>,Rag2<tm1Fwa>/Rag2<tm1Fwa>	involves: 129P2/OlaHsd * 129S/SvEv	N	10614672
MGI:3789200	F	MP:0004904	increased uterus weight	Apoe<tm1Unc>/Apoe<tm1Unc>,Rag2<tm1Fwa>/Rag2<+>	involves: 129P2/OlaHsd * 129S/SvEv	N	10614672
MGI:3789206	M	MP:0002216	abnormal seminiferous tubule morphology	Lama2<tm1Stk>/Lama2<tm1Stk>	involves: 129P2/OlaHsd	N	16127160
MGI:3789206	M	MP:0006380	abnormal spermatid morphology	Lama2<tm1Stk>/Lama2<tm1Stk>	involves: 129P2/OlaHsd	N	16127160
MGI:3789206	M	MP:0001146	abnormal testis morphology	Lama2<tm1Stk>/Lama2<tm1Stk>	involves: 129P2/OlaHsd	N	16127160
MGI:3789312	M	MP:0004852	decreased testis weight	Lama2<dy>/Lama2<dy>	B6.129P1-Lama2<dy>/J	N	1301630
MGI:3789490	M	MP:0005169	abnormal male meiosis	In(2)5Rk/+	involves: C57BL/6J * DBA/2J	N	4361911
MGI:3789490	F	MP:0001926	female infertility	In(2)5Rk/+	involves: C57BL/6J * DBA/2J	N	MGI:1277880
MGI:3789511	M	MP:0005169	abnormal male meiosis	In(1)1Rk/+	involves: C57BL/6J * DBA/2J	N	5289032
MGI:3789582	M	MP:0001925	male infertility	cod/cod	involves: BALB/cGr	N	MGI:62034
MGI:3789582	F	MP:0001926	female infertility	cod/cod	involves: BALB/cGr	N	MGI:62034
MGI:3789585	M	MP:0005169	abnormal male meiosis	In(15)18Rk/+	involves: C57BL/6J * DBA/2J	N	MGI:1277880
MGI:3789596	M	MP:0005169	abnormal male meiosis	In(5)2Rk/+	involves: C57BL/6J * DBA/2J	N	5289032
MGI:3789596	M	MP:0005169	abnormal male meiosis	In(5)2Rk/+	involves: C57BL/6J * DBA/2J	N	MGI:1277880
MGI:3789616	M	MP:0001922	reduced male fertility	In(5)9Rk/+	involves: C3H * DBA/2J	N	MGI:1277880
MGI:3789616	F	MP:0001923	reduced female fertility	In(5)9Rk/+	involves: C3H * DBA/2J	N	MGI:1277880
MGI:3789616	M	MP:0005169	abnormal male meiosis	In(5)9Rk/+	involves: C3H * DBA/2J	N	4361911
MGI:3789622	M	MP:0005169	abnormal male meiosis	In(10)6Rk/+	involves: C57BL/6J * DBA/2J	N	4361911
MGI:3789629	M	MP:0005169	abnormal male meiosis	In(2)19Rk/+	involves: C57BL/6J * DBA/2J	N	MGI:71289
MGI:3789693	M	MP:0005169	abnormal male meiosis	In(3)11Rk/+	involves: C57BL/6J	N	MGI:71289
MGI:3789697	M	MP:0005169	abnormal male meiosis	In(1)12Rk/+	involves: C57BL/6J	N	MGI:71289
MGI:3789907	M	MP:0005169	abnormal male meiosis	In(7)13Rk/+	involves: C3H * DBA/2J	N	MGI:71289
MGI:3789937	M	MP:0005169	abnormal male meiosis	In(8)14Rk/+	involves: C57BL/6J * DBA/2J	N	MGI:71289
MGI:3789959	M	MP:0005169	abnormal male meiosis	In(9)26Rk/+	involves: C57BL/6J * DBA/2J	N	MGI:71289
MGI:3789967	M	MP:0005169	abnormal male meiosis	In(4)28Rk/+	involves: M. m. domesticus poschiavinus	N	MGI:71289
MGI:3789971	M	MP:0005169	abnormal male meiosis	In(13)31Rk/+	Not Specified	N	MGI:71289
MGI:3789977	M	MP:0005169	abnormal male meiosis	In(4)32Rk/+	Not Specified	N	MGI:71289
MGI:3789982	M	MP:0005169	abnormal male meiosis	In(5)33Rk/+	involves: M. m. domesticus poschiavinus	N	MGI:71289
MGI:3790075	M	MP:0005169	abnormal male meiosis	In(15)21Rk/+	involves: C57BL/6J * DBA/2J	N	MGI:71289
MGI:3790075	M	MP:0004901	decreased male germ cell number	In(15)21Rk/+	involves: C57BL/6J * DBA/2J	N	385432
MGI:3790080	M	MP:0005169	abnormal male meiosis	In(14)22Rk/+	involves: C57BL/6J * DBA/2J	N	MGI:71289
MGI:3790087	M	MP:0005169	abnormal male meiosis	In(1)24Rk/+	involves: C57BL/6J * DBA/2J	N	MGI:71289
MGI:3790095	M	MP:0005169	abnormal male meiosis	In(12)25Rk/+	involves: C57BL/6J * DBA/2J	N	MGI:71289
MGI:3790321	F	MP:0001133	impaired luteal cell differentiation	Tg(Cga-LHB/CGB)94Jhn/?	involves: C57BL/6 * SJL	N	7877975
MGI:3790321	F	MP:0008000	increased ovary tumor incidence	Tg(Cga-LHB/CGB)94Jhn/?	involves: C57BL/6 * SJL	N	7877975
MGI:3790321	F	MP:0008869	anovulation	Tg(Cga-LHB/CGB)94Jhn/?	involves: C57BL/6 * SJL	N	7877975
MGI:3790321	F	MP:0004832	enlarged ovary	Tg(Cga-LHB/CGB)94Jhn/?	involves: C57BL/6 * SJL	N	7877975
MGI:3790321	F	MP:0001923	reduced female fertility	Tg(Cga-LHB/CGB)94Jhn/?	involves: C57BL/6 * SJL	N	7877975
MGI:3790321	M	MP:0001147	small testis	Tg(Cga-LHB/CGB)94Jhn/?	involves: C57BL/6 * SJL	N	7877975
MGI:3790321	F	MP:0002016	ovary cyst	Tg(Cga-LHB/CGB)94Jhn/?	involves: C57BL/6 * SJL	N	7877975
MGI:3790321	M	MP:0001922	reduced male fertility	Tg(Cga-LHB/CGB)94Jhn/?	involves: C57BL/6 * SJL	N	7877975
MGI:3790431	F	MP:0001130	abnormal ovarian folliculogenesis	Inha<tm1Bay>/Inha<tm1Bay>,Smad3<tm1Par>/Smad3<tm1Par>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/Sv * C57BL/6	N	17652186
MGI:3790431	M	MP:0002776	increased Sertoli cell number	Inha<tm1Bay>/Inha<tm1Bay>,Smad3<tm1Par>/Smad3<tm1Par>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/Sv * C57BL/6	N	17652186
MGI:3790431	F	MP:0008000	increased ovary tumor incidence	Inha<tm1Bay>/Inha<tm1Bay>,Smad3<tm1Par>/Smad3<tm1Par>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/Sv * C57BL/6	N	17652186
MGI:3790432	F	MP:0008000	increased ovary tumor incidence	Inha<tm1Bay>/Inha<tm1Bay>,Smad3<tm1Par>/Smad3<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/Sv * C57BL/6	N	17652186
MGI:3790441	M	MP:0005169	abnormal male meiosis	In(10)17Rk/+	involves: C57BL/6J * DBA/2J	N	MGI:71289
MGI:3790510	F	MP:0008000	increased ovary tumor incidence	Tom1l2<Gt(XG909)Byg>/Tom1l2<Gt(XG909)Byg>	involves: 129P2/OlaHsd * C57BL/6J	N	18343975
MGI:3790510	M	MP:0010357	increased prostate gland tumor incidence	Tom1l2<Gt(XG909)Byg>/Tom1l2<Gt(XG909)Byg>	involves: 129P2/OlaHsd * C57BL/6J	N	18343975
MGI:3790600	M	MP:0010357	increased prostate gland tumor incidence	Tom1l2<Gt(XG909)Byg>/Tom1l2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	18343975
MGI:3790600	F	MP:0002016	ovary cyst	Tom1l2<Gt(XG909)Byg>/Tom1l2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	18343975
MGI:3790650	M	MP:0001861	lung inflammation	Il10<tm1Roer>/Il10<tm1Roer>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18387831
MGI:3790650	M	MP:0002816	colitis	Il10<tm1Roer>/Il10<tm1Roer>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18387831
MGI:3790650	M	MP:0008661	decreased interleukin-10 secretion	Il10<tm1Roer>/Il10<tm1Roer>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18387831
MGI:3790650	M	MP:0004946	abnormal regulatory T cell physiology	Il10<tm1Roer>/Il10<tm1Roer>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18387831
MGI:3790650	M	MP:0002534	abnormal type IV hypersensitivity reaction	Il10<tm1Roer>/Il10<tm1Roer>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18387831
MGI:3790875	M	MP:0031391	increased locomotor activity	Chrna2<tm1Jbou>/Chrna2<tm1Jbou>	B6.129X1-Chrna2<tm1Jbou>	N	28507032
MGI:3790875	M	MP:0005378	growth/size/body region phenotype	Chrna2<tm1Jbou>/Chrna2<tm1Jbou>	B6.129X1-Chrna2<tm1Jbou>	Y	28507032
MGI:3790875	M	MP:0005380	embryo phenotype	Chrna2<tm1Jbou>/Chrna2<tm1Jbou>	B6.129X1-Chrna2<tm1Jbou>	Y	28507032
MGI:3790875	M	MP:0005386	behavior/neurological phenotype	Chrna2<tm1Jbou>/Chrna2<tm1Jbou>	B6.129X1-Chrna2<tm1Jbou>	Y	28507032
MGI:3790875	M	MP:0009454	impaired contextual conditioning behavior	Chrna2<tm1Jbou>/Chrna2<tm1Jbou>	B6.129X1-Chrna2<tm1Jbou>	N	28507032
MGI:3790954	F	MP:0004868	increased endometrial carcinoma incidence	Stk11<tm1Tpm>/Stk11<+>	Not Specified	N	12218179
MGI:3790961	M	MP:0010357	increased prostate gland tumor incidence	Klrk1<tm1Dhr>/Klrk1<tm1Dhr>,Tg(TRAMP)8247Ng/?	involves: C57BL/6 * CD-1	N	18394936
MGI:3790971	M	MP:0031286	unilateral cryptorchism	Lrp2<tm1Her>/Lrp2<tm1Her>	either: (involves: 129S7/SvEvBrd * CD-1) or (involves: 129/SvEmcTer * 129S7/SvEvBrd * C57BL/6N)	N	16143106
MGI:3790971	M	MP:0001146	abnormal testis morphology	Lrp2<tm1Her>/Lrp2<tm1Her>	either: (involves: 129S7/SvEvBrd * CD-1) or (involves: 129/SvEmcTer * 129S7/SvEvBrd * C57BL/6N)	N	16143106
MGI:3790971	M	MP:0003830	abnormal testis development	Lrp2<tm1Her>/Lrp2<tm1Her>	either: (involves: 129S7/SvEvBrd * CD-1) or (involves: 129/SvEmcTer * 129S7/SvEvBrd * C57BL/6N)	N	16143106
MGI:3790971	F	MP:0001123	dilated uterus	Lrp2<tm1Her>/Lrp2<tm1Her>	either: (involves: 129S7/SvEvBrd * CD-1) or (involves: 129/SvEmcTer * 129S7/SvEvBrd * C57BL/6N)	N	16143106
MGI:3790971	F	MP:0009708	vaginal septum	Lrp2<tm1Her>/Lrp2<tm1Her>	either: (involves: 129S7/SvEvBrd * CD-1) or (involves: 129/SvEmcTer * 129S7/SvEvBrd * C57BL/6N)	N	16143106
MGI:3793277	F	MP:0001923	reduced female fertility	Atp7b<tx>/Atp7b<tx>	DL-Atp7b<tx>	N	6863890
MGI:3793278	F	MP:0001923	reduced female fertility	Atp7b<tx>/Atp7b<tx>	involves: C57BL/6 * DL	N	6863890
MGI:3793282	M	MP:0002687	oligozoospermia	Ror2<tm1Anec>/Ror2<tm1Anec>	B6.129S1-Ror2<tm1Anec>	N	18353862
MGI:3793282	M	MP:0004852	decreased testis weight	Ror2<tm1Anec>/Ror2<tm1Anec>	B6.129S1-Ror2<tm1Anec>	N	18353862
MGI:3793282	M	MP:0002216	abnormal seminiferous tubule morphology	Ror2<tm1Anec>/Ror2<tm1Anec>	B6.129S1-Ror2<tm1Anec>	N	18353862
MGI:3793282	M	MP:0001153	small seminiferous tubules	Ror2<tm1Anec>/Ror2<tm1Anec>	B6.129S1-Ror2<tm1Anec>	N	18353862
MGI:3793282	M	MP:0001922	reduced male fertility	Ror2<tm1Anec>/Ror2<tm1Anec>	B6.129S1-Ror2<tm1Anec>	N	18353862
MGI:3793422	F	MP:0012411	increased granulosa cell tumor incidence	Bin1<tm1Gcp>/Bin1<tm2Gcp>,Tg(Wap-cre)11738Mam/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	N	17210688
MGI:3793422	F	MP:0006271	abnormal involution of the mammary gland	Bin1<tm1Gcp>/Bin1<tm2Gcp>,Tg(Wap-cre)11738Mam/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	N	17210688
MGI:3793422	F	MP:0004135	abnormal mammary gland embryonic development	Bin1<tm1Gcp>/Bin1<tm2Gcp>,Tg(Wap-cre)11738Mam/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	N	17210688
MGI:3793701	M	MP:0003608	prostate gland inflammation	Aire<tm1.1Doi>/Aire<tm1.1Doi>	NOD.129S2(B6)-Aire<tm1.1Doi>/Doi	N	16172259
MGI:3793701	F	MP:0001868	ovary inflammation	Aire<tm1.1Doi>/Aire<tm1.1Doi>	NOD.129S2(B6)-Aire<tm1.1Doi>/Doi	N	16172259
MGI:3793702	F	MP:0001868	ovary inflammation	Aire<tm1.1Doi>/Aire<tm1.1Doi>	C.129S2-Aire<tm1.1Doi>/Doi	N	16172259
MGI:3793702	M	MP:0003608	prostate gland inflammation	Aire<tm1.1Doi>/Aire<tm1.1Doi>	C.129S2-Aire<tm1.1Doi>/Doi	N	16172259
MGI:3793703	F	MP:0001868	ovary inflammation	Aire<tm1.1Doi>/Aire<tm1.1Doi>	SJL.129S2-Aire<tm1.1Doi>/Doi	N	16172259
MGI:3793703	M	MP:0003608	prostate gland inflammation	Aire<tm1.1Doi>/Aire<tm1.1Doi>	SJL.129S2-Aire<tm1.1Doi>/Doi	N	16172259
MGI:3793722	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-12DFiOD>/Y	involves: 101 * C3H * T STOCK	N	9147646
MGI:3793723	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-1Pub>/Y	involves: 101 * C3H * T STOCK	N	9147646
MGI:3793724	M	MP:0011085	postnatal lethality, complete penetrance	Atp7a<Mo-2Acre>/Y	involves: 101 * C3H * T STOCK	N	9147646
MGI:3793725	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-8R>/Y	involves: 101 * C3H * T STOCK	N	9147646
MGI:3793726	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-7R>/Y	Not Specified	N	9147646
MGI:3793727	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-7ENURF>/Y	Not Specified	N	9147646
MGI:3793728	M	MP:0002083	premature death	Atp7a<Mo-blo>/Y	Not Specified	N	MGI:61583
MGI:3793728	M	MP:0001925	male infertility	Atp7a<Mo-blo>/Y	Not Specified	N	MGI:61583
MGI:3793728	M	MP:0001274	curly vibrissae	Atp7a<Mo-blo>/Y	Not Specified	N	MGI:61583
MGI:3793728	M	MP:0005150	cachexia	Atp7a<Mo-blo>/Y	Not Specified	N	1115218
MGI:3793728	M	MP:0031200	increased aortic weight	Atp7a<Mo-blo>/Y	Not Specified	N	4808708
MGI:3793728	M	MP:0010574	dilated aorta	Atp7a<Mo-blo>/Y	Not Specified	N	1115218
MGI:3793728	M	MP:0006278	aortic aneurysm	Atp7a<Mo-blo>/Y	Not Specified	N	4808708
MGI:3793728	M	MP:0001505	hunched posture	Atp7a<Mo-blo>/Y	Not Specified	N	1115218
MGI:3793728	M	MP:0010470	dilated ascending aorta	Atp7a<Mo-blo>/Y	Not Specified	N	3385878
MGI:3793728	M	MP:0000371	diluted coat color	Atp7a<Mo-blo>/Y	Not Specified	N	MGI:61583
MGI:3793728	M	MP:0006278	aortic aneurysm	Atp7a<Mo-blo>/Y	Not Specified	N	3385878
MGI:3793728	M	MP:0003964	abnormal noradrenaline level	Atp7a<Mo-blo>/Y	Not Specified	N	4858102
MGI:3793728	M	MP:0001265	decreased body size	Atp7a<Mo-blo>/Y	Not Specified	N	MGI:61583
MGI:3793728	M	MP:0000371	diluted coat color	Atp7a<Mo-blo>/Y	Not Specified	N	4858102
MGI:3793728	M	MP:0005243	hemothorax	Atp7a<Mo-blo>/Y	Not Specified	N	1115218
MGI:3793728	M	MP:0000371	diluted coat color	Atp7a<Mo-blo>/Y	Not Specified	N	3385878
MGI:3793728	M	MP:0000745	tremors	Atp7a<Mo-blo>/Y	Not Specified	N	4858102
MGI:3793728	M	MP:0010768	mortality/aging	Atp7a<Mo-blo>/Y	Not Specified	Y	9147646
MGI:3793728	M	MP:0003415	priapism	Atp7a<Mo-blo>/Y	Not Specified	N	1115218
MGI:3793728	M	MP:0001402	decreased locomotor activity	Atp7a<Mo-blo>/Y	Not Specified	N	4858102
MGI:3793728	M	MP:0003907	decreased aorta elastin content	Atp7a<Mo-blo>/Y	Not Specified	N	1115218
MGI:3793728	M	MP:0000556	abnormal hindlimb morphology	Atp7a<Mo-blo>/Y	Not Specified	N	MGI:61583
MGI:3793728	M	MP:0005202	lethargy	Atp7a<Mo-blo>/Y	Not Specified	N	1115218
MGI:3793728	M	MP:0002832	coarse hair	Atp7a<Mo-blo>/Y	Not Specified	N	1115218
MGI:3793728	M	MP:0000272	abnormal aorta morphology	Atp7a<Mo-blo>/Y	Not Specified	N	3385878
MGI:3793728	M	MP:0003211	abnormal aorta elastic fiber morphology	Atp7a<Mo-blo>/Y	Not Specified	N	1115218
MGI:3793728	M	MP:0000272	abnormal aorta morphology	Atp7a<Mo-blo>/Y	Not Specified	N	4808708
MGI:3793728	M	MP:0006278	aortic aneurysm	Atp7a<Mo-blo>/Y	Not Specified	N	1115218
MGI:3793729	M	MP:0002083	premature death	Atp7a<Mo-vbr>/Y	Not Specified	N	9147646
MGI:3793729	M	MP:0004043	abnormal pH regulation	Atp7a<Mo-vbr>/Y	Not Specified	N	9342151
MGI:3793729	M	MP:0031200	increased aortic weight	Atp7a<Mo-vbr>/Y	Not Specified	N	4808708
MGI:3793729	M	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-vbr>/Y	Not Specified	N	MGI:61663
MGI:3793729	M	MP:0002082	postnatal lethality	Atp7a<Mo-vbr>/Y	Not Specified	N	9147646
MGI:3793729	M	MP:0010062	decreased creatine level	Atp7a<Mo-vbr>/Y	Not Specified	N	9342151
MGI:3793729	M	MP:0001191	abnormal skin condition	Atp7a<Mo-vbr>/Y	Not Specified	N	4808708
MGI:3793729	M	MP:0006036	abnormal mitochondrial physiology	Atp7a<Mo-vbr>/Y	Not Specified	N	9342151
MGI:3793729	M	MP:0000272	abnormal aorta morphology	Atp7a<Mo-vbr>/Y	Not Specified	N	4808708
MGI:3793729	M	MP:0003211	abnormal aorta elastic fiber morphology	Atp7a<Mo-vbr>/Y	Not Specified	N	4808708
MGI:3793729	M	MP:0003089	decreased skin tensile strength	Atp7a<Mo-vbr>/Y	Not Specified	N	4808708
MGI:3793729	M	MP:0001925	male infertility	Atp7a<Mo-vbr>/Y	Not Specified	N	MGI:61663
MGI:3793729	M	MP:0008438	abnormal cutaneous collagen fibril morphology	Atp7a<Mo-vbr>/Y	Not Specified	N	4808708
MGI:3793729	M	MP:0006278	aortic aneurysm	Atp7a<Mo-vbr>/Y	Not Specified	N	4808708
MGI:3793729	M	MP:0005376	homeostasis/metabolism phenotype	Atp7a<Mo-vbr>/Y	Not Specified	Y	4808708
MGI:3793729	M	MP:0005584	abnormal enzyme/coenzyme activity	Atp7a<Mo-vbr>/Y	Not Specified	N	9342151
MGI:3793729	M	MP:0005584	abnormal enzyme/coenzyme activity	Atp7a<Mo-vbr>/Y	Not Specified	N	10098864
MGI:3793729	M	MP:0020308	decreased creatine kinase activity	Atp7a<Mo-vbr>/Y	Not Specified	N	9342151
MGI:3793730	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-Xm>/Y	Not Specified	N	9147646
MGI:3793780	M	MP:0003065	abnormal liver copper level	Atp7a<Mo-br>/Y	involves: C57BL	N	4858102
MGI:3793780	M	MP:0003964	abnormal noradrenaline level	Atp7a<Mo-br>/Y	involves: C57BL	N	4858102
MGI:3793780	M	MP:0010247	increased intestine copper level	Atp7a<Mo-br>/Y	involves: C57BL	N	4858102
MGI:3793780	M	MP:0011215	decreased brain copper level	Atp7a<Mo-br>/Y	involves: C57BL	N	4858102
MGI:3793780	M	MP:0006349	decreased circulating copper level	Atp7a<Mo-br>/Y	involves: C57BL	N	4858102
MGI:3793781	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-4R>/Y	Not Specified	N	MGI:61583
MGI:3793782	F	MP:0001278	kinked vibrissae	Atp7a<Mo-4R>/Atp7a<+>	Not Specified	N	MGI:61583
MGI:3793782	F	MP:0000421	mottled coat	Atp7a<Mo-4R>/Atp7a<+>	Not Specified	N	MGI:61583
MGI:3793784	F	MP:0005202	lethargy	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	1115218
MGI:3793784	F	MP:0005243	hemothorax	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	1115218
MGI:3793784	F	MP:0003279	aneurysm	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	1115218
MGI:3793784	F	MP:0001265	decreased body size	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	MGI:61583
MGI:3793784	F	MP:0006278	aortic aneurysm	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	1115218
MGI:3793784	F	MP:0010574	dilated aorta	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	1115218
MGI:3793784	F	MP:0006278	aortic aneurysm	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	4808708
MGI:3793784	F	MP:0001274	curly vibrissae	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	MGI:61583
MGI:3793784	F	MP:0000272	abnormal aorta morphology	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	1115218
MGI:3793784	F	MP:0005435	hemoperitoneum	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	1115218
MGI:3793784	F	MP:0003907	decreased aorta elastin content	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	1115218
MGI:3793784	F	MP:0002832	coarse hair	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	1115218
MGI:3793784	F	MP:0003211	abnormal aorta elastic fiber morphology	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	1115218
MGI:3793784	F	MP:0005150	cachexia	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	1115218
MGI:3793784	F	MP:0000556	abnormal hindlimb morphology	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	MGI:61583
MGI:3793784	F	MP:0001505	hunched posture	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	1115218
MGI:3793784	F	MP:0000371	diluted coat color	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	N	MGI:61583
MGI:3793784	F	MP:0005389	reproductive system phenotype	Atp7a<Mo-blo>/Atp7a<+>	Not Specified	Y	MGI:61583
MGI:3793785	F	MP:0001274	curly vibrissae	Atp7a<Mo-blo>/Atp7a<Mo-blo>	Not Specified	N	MGI:61583
MGI:3793785	F	MP:0000556	abnormal hindlimb morphology	Atp7a<Mo-blo>/Atp7a<Mo-blo>	Not Specified	N	MGI:61583
MGI:3793785	F	MP:0001926	female infertility	Atp7a<Mo-blo>/Atp7a<Mo-blo>	Not Specified	N	MGI:61583
MGI:3793785	F	MP:0000371	diluted coat color	Atp7a<Mo-blo>/Atp7a<Mo-blo>	Not Specified	N	MGI:61583
MGI:3793785	F	MP:0006278	aortic aneurysm	Atp7a<Mo-blo>/Atp7a<Mo-blo>	Not Specified	N	4808708
MGI:3793785	F	MP:0002083	premature death	Atp7a<Mo-blo>/Atp7a<Mo-blo>	Not Specified	N	MGI:61583
MGI:3793785	F	MP:0001265	decreased body size	Atp7a<Mo-blo>/Atp7a<Mo-blo>	Not Specified	N	MGI:61583
MGI:3793864	M	MP:0003560	osteoarthritis	Atp7a<Mo-blo>/Y	B6.Cg-Atp7a<Mo-blo>/J	N	8895222
MGI:3793864	M	MP:0003674	oxidative stress	Atp7a<Mo-blo>/Y	B6.Cg-Atp7a<Mo-blo>/J	N	16371425
MGI:3793864	M	MP:0000163	abnormal cartilage morphology	Atp7a<Mo-blo>/Y	B6.Cg-Atp7a<Mo-blo>/J	N	8895222
MGI:3793865	M	MP:0005584	abnormal enzyme/coenzyme activity	Atp7a<Mo-br>/Y	C57BL/6-Atp7a<Mo-br>/J	N	16371425
MGI:3794522	F	MP:0005508	abnormal skeleton morphology	Atp7a<Mo-dp>/Atp7a<+>	Not Specified	N	MGI:61157
MGI:3794522	F	MP:0005366	variegated coat color	Atp7a<Mo-dp>/Atp7a<+>	Not Specified	N	MGI:61157
MGI:3794522	F	MP:0001274	curly vibrissae	Atp7a<Mo-dp>/Atp7a<+>	Not Specified	N	MGI:61157
MGI:3794522	F	MP:0000576	clubfoot	Atp7a<Mo-dp>/Atp7a<+>	Not Specified	N	MGI:61157
MGI:3794522	F	MP:0006278	aortic aneurysm	Atp7a<Mo-dp>/Atp7a<+>	Not Specified	N	4808708
MGI:3794523	F	MP:0001279	wavy vibrissae	Atp7a<Mo-to>/Atp7a<+>	Not Specified	N	MGI:72704
MGI:3794523	F	MP:0006278	aortic aneurysm	Atp7a<Mo-to>/Atp7a<+>	Not Specified	N	4808708
MGI:3794523	F	MP:0005366	variegated coat color	Atp7a<Mo-to>/Atp7a<+>	Not Specified	N	MGI:72704
MGI:3794523	F	MP:0002074	abnormal hair texture	Atp7a<Mo-to>/Atp7a<+>	Not Specified	N	MGI:72704
MGI:3794523	F	MP:0002115	abnormal limb bone morphology	Atp7a<Mo-to>/Atp7a<+>	Not Specified	N	MGI:72704
MGI:3794524	M	MP:0006278	aortic aneurysm	Atp7a<Mo-to>/Y	Not Specified	N	4808708
MGI:3794524	M	MP:0002080	prenatal lethality	Atp7a<Mo-to>/Y	Not Specified	N	MGI:72704
MGI:3794525	F	MP:0006278	aortic aneurysm	Atp7a<Mo-blo>/Atp7a<Mo-br>	involves: C57BL	N	4808708
MGI:3794526	M	MP:0010895	increased lung compliance	Atp7a<Mo-blo>/Y	involves: C57BL/10	N	937819
MGI:3794526	M	MP:0010900	abnormal pulmonary interalveolar septum morphology	Atp7a<Mo-blo>/Y	involves: C57BL/10	N	937819
MGI:3794526	M	MP:0010908	dilated pulmonary alveolar duct	Atp7a<Mo-blo>/Y	involves: C57BL/10	N	937819
MGI:3794526	M	MP:0010937	increased total lung capacity	Atp7a<Mo-blo>/Y	involves: C57BL/10	N	937819
MGI:3794526	M	MP:0002133	abnormal respiratory system physiology	Atp7a<Mo-blo>/Y	involves: C57BL/10	N	937819
MGI:3794526	M	MP:0002270	abnormal pulmonary alveolus morphology	Atp7a<Mo-blo>/Y	involves: C57BL/10	N	937819
MGI:3794526	M	MP:0001951	abnormal breathing pattern	Atp7a<Mo-blo>/Y	involves: C57BL/10	N	937819
MGI:3794526	M	MP:0004882	enlarged lung	Atp7a<Mo-blo>/Y	involves: C57BL/10	N	937819
MGI:3794526	M	MP:0010856	dilated respiratory conducting tube	Atp7a<Mo-blo>/Y	involves: C57BL/10	N	937819
MGI:3794967	M	MP:0004852	decreased testis weight	Tex15<tm1Jw>/Tex15<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	18283110
MGI:3794967	M	MP:0001156	abnormal spermatogenesis	Tex15<tm1Jw>/Tex15<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	18283110
MGI:3794967	M	MP:0004901	decreased male germ cell number	Tex15<tm1Jw>/Tex15<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	18283110
MGI:3794967	M	MP:0001925	male infertility	Tex15<tm1Jw>/Tex15<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	18283110
MGI:3794967	M	MP:0008261	arrest of male meiosis	Tex15<tm1Jw>/Tex15<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	18283110
MGI:3794971	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(MMTV-TGFBR2)7Hlm/0	involves: C57BL/6 * DBA	N	9543389
MGI:3794971	F	MP:0001882	abnormal lactation	Tg(MMTV-TGFBR2)7Hlm/0	involves: C57BL/6 * DBA	N	9543389
MGI:3794972	F	MP:0013716	hypolactation	Tg(MMTV-TGFBR2)7Hlm/Tg(MMTV-TGFBR2)7Hlm	involves: C57BL/6 * DBA	N	14507660
MGI:3794972	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(MMTV-TGFBR2)7Hlm/Tg(MMTV-TGFBR2)7Hlm	involves: C57BL/6 * DBA	N	14507660
MGI:3794972	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(MMTV-TGFBR2)7Hlm/Tg(MMTV-TGFBR2)7Hlm	involves: C57BL/6 * DBA	N	9543389
MGI:3794972	F	MP:0006271	abnormal involution of the mammary gland	Tg(MMTV-TGFBR2)7Hlm/Tg(MMTV-TGFBR2)7Hlm	involves: C57BL/6 * DBA	N	14507660
MGI:3794972	F	MP:0001882	abnormal lactation	Tg(MMTV-TGFBR2)7Hlm/Tg(MMTV-TGFBR2)7Hlm	involves: C57BL/6 * DBA	N	9543389
MGI:3794972	F	MP:0003344	mammary gland hypoplasia	Tg(MMTV-TGFBR2)7Hlm/Tg(MMTV-TGFBR2)7Hlm	involves: C57BL/6 * DBA	N	14507660
MGI:3794972	F	MP:0006270	abnormal mammary gland growth during lactation	Tg(MMTV-TGFBR2)7Hlm/Tg(MMTV-TGFBR2)7Hlm	involves: C57BL/6 * DBA	N	14507660
MGI:3795127	F	MP:0001393	ataxia	Gria3<tm1Dgen>/Gria3<tm1Dgen>,Gria4<spkw1>/Gria4<spkw1>	involves: 129P2/OlaHsd * C3H/HeJ * C57BL/6J	N	18316356
MGI:3795127	F	MP:0003216	absence seizures	Gria3<tm1Dgen>/Gria3<tm1Dgen>,Gria4<spkw1>/Gria4<spkw1>	involves: 129P2/OlaHsd * C3H/HeJ * C57BL/6J	N	18316356
MGI:3795130	F	MP:0005386	behavior/neurological phenotype	Gria3<tm1Dgen>/Gria3<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	Y	18316356
MGI:3795243	F	MP:0012009	early parturition	Cnr1<tm1Zim>/Cnr1<tm1Zim>	involves: 129 * C57BL/6J	N	18833324
MGI:3795272	F	MP:0005431	decreased oocyte number	Rspo1<tm1.1Ktom>/Rspo1<tm1.1Ktom>	involves: C57BL/6 * CBA	N	18250097
MGI:3795272	F	MP:0002783	abnormal ovary secretion	Rspo1<tm1.1Ktom>/Rspo1<tm1.1Ktom>	involves: C57BL/6 * CBA	N	18250097
MGI:3795272	F	MP:0001923	reduced female fertility	Rspo1<tm1.1Ktom>/Rspo1<tm1.1Ktom>	involves: C57BL/6 * CBA	N	18250097
MGI:3795272	F	MP:0002682	decreased mature ovarian follicle number	Rspo1<tm1.1Ktom>/Rspo1<tm1.1Ktom>	involves: C57BL/6 * CBA	N	18250097
MGI:3795272	F	MP:0003582	abnormal ovary development	Rspo1<tm1.1Ktom>/Rspo1<tm1.1Ktom>	involves: C57BL/6 * CBA	N	18250097
MGI:3795283	F	MP:0005168	abnormal female meiosis	Rspo1<tm1Mcch>/Rspo1<tm1Mcch>	involves: 129 * C57BL/6J	N	18250098
MGI:3795283	F	MP:0003582	abnormal ovary development	Rspo1<tm1Mcch>/Rspo1<tm1Mcch>	involves: 129 * C57BL/6J	N	18250098
MGI:3795359	M	MP:0002686	globozoospermia	Brwd1<Gt(AW0417)Wtsi>/Brwd1<repro5>	involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3795359	M	MP:0002675	asthenozoospermia	Brwd1<Gt(AW0417)Wtsi>/Brwd1<repro5>	involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3795359	M	MP:0004901	decreased male germ cell number	Brwd1<Gt(AW0417)Wtsi>/Brwd1<repro5>	involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J	N	18353305
MGI:3795360	M	MP:0006362	abnormal male germ cell morphology	Brwd1<Gt(AW0417)Wtsi>/Brwd1<Gt(AW0417)Wtsi>	involves: 129P2/OlaHsd	N	18353305
MGI:3795360	M	MP:0004901	decreased male germ cell number	Brwd1<Gt(AW0417)Wtsi>/Brwd1<Gt(AW0417)Wtsi>	involves: 129P2/OlaHsd	N	18353305
MGI:3795360	F	MP:0005168	abnormal female meiosis	Brwd1<Gt(AW0417)Wtsi>/Brwd1<Gt(AW0417)Wtsi>	involves: 129P2/OlaHsd	N	18353305
MGI:3795453	F	MP:0001728	failure of embryo implantation	Cdc73<Gt(RRE190)Byg>/Cdc73<Gt(RRE190)Byg>	involves: 129P2/OlaHsd	N	18212049
MGI:3795455	M	MP:0001157	small seminal vesicle	Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129S4/SvJae * C57BL/6 * CBA	N	18212049
MGI:3795455	M	MP:0001147	small testis	Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129S4/SvJae * C57BL/6 * CBA	N	18212049
MGI:3795482	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Psca<tm1Witt>/Psca<tm1Witt>,Tg(TRAMP)8247Ng/0	involves: 129/Sv * C57BL/6	N	18044730
MGI:3795482	M	MP:0010357	increased prostate gland tumor incidence	Psca<tm1Witt>/Psca<tm1Witt>,Tg(TRAMP)8247Ng/0	involves: 129/Sv * C57BL/6	N	18044730
MGI:3795482	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Psca<tm1Witt>/Psca<tm1Witt>,Tg(TRAMP)8247Ng/0	involves: 129/Sv * C57BL/6	N	18044730
MGI:3795484	M	MP:0010357	increased prostate gland tumor incidence	Psca<tm1Witt>/Psca<+>,Tg(TRAMP)8247Ng/0	involves: 129/Sv * C57BL/6	N	18044730
MGI:3795484	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Psca<tm1Witt>/Psca<+>,Tg(TRAMP)8247Ng/0	involves: 129/Sv * C57BL/6	N	18044730
MGI:3795484	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Psca<tm1Witt>/Psca<+>,Tg(TRAMP)8247Ng/0	involves: 129/Sv * C57BL/6	N	18044730
MGI:3795485	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(TRAMP)8247Ng/0	involves: 129/Sv * C57BL/6	N	18044730
MGI:3795485	M	MP:0010357	increased prostate gland tumor incidence	Tg(TRAMP)8247Ng/0	involves: 129/Sv * C57BL/6	N	18044730
MGI:3795485	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(TRAMP)8247Ng/0	involves: 129/Sv * C57BL/6	N	18044730
MGI:3795485	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(TRAMP)8247Ng/0	involves: 129/Sv * C57BL/6	N	18245377
MGI:3795496	F	MP:0001926	female infertility	Dnmt1<tm1Jrc>/Dnmt1<tm1Jrc>	involves: 129S1/Sv	N	11290321
MGI:3795687	F	MP:0013785	abnormal mammary gland bud morphology	Gli2<tm3(Gli1)Alj>/Gli2<tm3(Gli1)Alj>,Gli3<Xt-J>/Gli3<+>	involves: 129S6/SvEvTac * Black Swiss * C3H/HeJ * C57BL/6 * Swiss Webster	N	16914490
MGI:3795690	F	MP:0013785	abnormal mammary gland bud morphology	Gli2<tm2.1Alj>/Gli2<+>,Gli3<Xt-J>/Gli3<Xt-J>	involves: 129S6/SvEvTac * Black Swiss * C3H/HeJ * C57BL/6 * Swiss Webster	N	16914490
MGI:3795691	F	MP:0004135	abnormal mammary gland embryonic development	Gli3<Xt-J>/Gli3<Xt-J>,Tg(TCF/Lef1-lacZ)34Efu/0	involves: C3H/HeJ * C57BL/6	N	16914490
MGI:3795691	F	MP:0013721	abnormal mammary placode morphology	Gli3<Xt-J>/Gli3<Xt-J>,Tg(TCF/Lef1-lacZ)34Efu/0	involves: C3H/HeJ * C57BL/6	N	16914490
MGI:3795861	M	MP:0002757	decreased vertical activity	Selenop<tm1Rfb>/Selenop<tm1Rfb>	B6.129-Selenop<tm1Rfb>	N	22487427
MGI:3795861	M	MP:0010053	decreased grip strength	Selenop<tm1Rfb>/Selenop<tm1Rfb>	B6.129-Selenop<tm1Rfb>	N	22487427
MGI:3795862	M	MP:0014464	decreased sperm mitochondrial sheath size	Selenop<tm2Rfb>/Selenop<tm2Rfb>	B6.Cg-Selenop<tm2Rfb>	N	17311913
MGI:3795862	M	MP:0001922	reduced male fertility	Selenop<tm2Rfb>/Selenop<tm2Rfb>	B6.Cg-Selenop<tm2Rfb>	N	17311913
MGI:3795862	M	MP:0009831	abnormal sperm midpiece morphology	Selenop<tm2Rfb>/Selenop<tm2Rfb>	B6.Cg-Selenop<tm2Rfb>	N	17311913
MGI:3795862	M	MP:0008892	abnormal sperm flagellum morphology	Selenop<tm2Rfb>/Selenop<tm2Rfb>	B6.Cg-Selenop<tm2Rfb>	N	17311913
MGI:3795862	M	MP:0009243	hairpin sperm flagellum	Selenop<tm2Rfb>/Selenop<tm2Rfb>	B6.Cg-Selenop<tm2Rfb>	N	17311913
MGI:3795904	M	MP:0013317	abnormal seminal vesicle development	Lactb2<Tg(Igh-Meis1)2770Amb>/Lactb2<Tg(Igh-Meis1)2770Amb>	FVB/NJ-Lactb2<Tg(Igh-Meis1)2770Amb>	N	12374767
MGI:3795905	F	MP:0010768	mortality/aging	Ar<Tfm>/Ar<+>,Lactb2<Tg(Igh-Meis1)2770Amb>/Lactb2<Tg(Igh-Meis1)2770Amb>	involves: FVB/NJ	Y	12374767
MGI:3796061	M	MP:0001925	male infertility	Kcnn2<bc>/Kcnn2<bc>	Not Specified	N	6949984
MGI:3796071	M	MP:0001925	male infertility	Kcnn2<bc-3J>/Kcnn2<bc-3J>	C3H/HeSn-bc<3J>	N	6949984
MGI:3796134	F	MP:0002169	no abnormal phenotype detected	Mirc2<tm1.1Tyj>/Mirc2<tm1.1Tyj>	involves: 129S4/SvJae * C57BL/6 * SJL	N	18329372
MGI:3796135	F	MP:0002169	no abnormal phenotype detected	Mirc2<tm1Tyj>/Mirc2<tm1Tyj>	involves: 129S4/SvJae * C57BL/6	N	18329372
MGI:3796136	F	MP:0001926	female infertility	Tmprss6<msk>/Tmprss6<msk>	C57BL/6J-Tmprss6<msk>	N	18451267
MGI:3796152	M	MP:0000280	thin ventricular wall	Mirc2<tm1.1Tyj>/Y,Mirc3<tm1.1Tyj>/Mirc3<tm1.1Tyj>,Mirc1<tm1.2Tyj>/Mirc1<tm1.2Tyj>	involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL	N	18329372
MGI:3796152	M	MP:0011091	prenatal lethality, complete penetrance	Mirc2<tm1.1Tyj>/Y,Mirc3<tm1.1Tyj>/Mirc3<tm1.1Tyj>,Mirc1<tm1.2Tyj>/Mirc1<tm1.2Tyj>	involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL	N	18329372
MGI:3796152	M	MP:0010402	ventricular septal defect	Mirc2<tm1.1Tyj>/Y,Mirc3<tm1.1Tyj>/Mirc3<tm1.1Tyj>,Mirc1<tm1.2Tyj>/Mirc1<tm1.2Tyj>	involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL	N	18329372
MGI:3796152	M	MP:0010403	atrial septal defect	Mirc2<tm1.1Tyj>/Y,Mirc3<tm1.1Tyj>/Mirc3<tm1.1Tyj>,Mirc1<tm1.2Tyj>/Mirc1<tm1.2Tyj>	involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL	N	18329372
MGI:3796152	M	MP:0006042	increased apoptosis	Mirc2<tm1.1Tyj>/Y,Mirc3<tm1.1Tyj>/Mirc3<tm1.1Tyj>,Mirc1<tm1.2Tyj>/Mirc1<tm1.2Tyj>	involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL	N	18329372
MGI:3796153	M	MP:0002169	no abnormal phenotype detected	Mirc2<tm1.1Tyj>/Y,Mirc3<tm1.1Tyj>/Mirc3<tm1.1Tyj>,Mirc1<tm1.2Tyj>/Mirc1<+>	involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL	N	18329372
MGI:3796418	M	MP:0000186	decreased circulating HDL cholesterol level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0004910	decreased seminal vesicle weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12185100
MGI:3796418	M	MP:0004910	decreased seminal vesicle weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10067829
MGI:3796418	F	MP:0002636	delayed vaginal opening	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10342852
MGI:3796418	F	MP:0002680	decreased corpora lutea number	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	M	MP:0005669	increased circulating leptin level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	F	MP:0001729	impaired embryo implantation	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	M	MP:0005458	increased percent body fat/body weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0005449	abnormal food intake	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0011939	increased food intake	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	F	MP:0002682	decreased mature ovarian follicle number	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	F	MP:0003507	abnormal ovary physiology	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	M	MP:0009304	increased retroperitoneal fat pad weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0002176	increased brain weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0003055	abnormal long bone epiphyseal plate morphology	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10631109
MGI:3796418	M	MP:0002644	decreased circulating triglyceride level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	F	MP:0002891	increased insulin sensitivity	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10974652
MGI:3796418	F	MP:0001935	decreased litter size	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	9371826
MGI:3796418	F	MP:0001938	delayed sexual maturation	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	M	MP:0001938	delayed sexual maturation	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12185100
MGI:3796418	M	MP:0002113	abnormal skeleton development	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10631109
MGI:3796418	F	MP:0001938	delayed sexual maturation	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10342852
MGI:3796418	F	MP:0001129	impaired ovarian folliculogenesis	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	M	MP:0005473	decreased triiodothyronine level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10631109
MGI:3796418	M	MP:0008938	decreased pituitary gland weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10067829
MGI:3796418	M	MP:0014269	decreased testes secretion	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10067829
MGI:3796418	M	MP:0008940	delayed balanopreputial separation	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12185100
MGI:3796418	M	MP:0004908	abnormal seminal vesicle weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12185100
MGI:3796418	F	MP:0002727	decreased circulating insulin level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10974652
MGI:3796418	M	MP:0002727	decreased circulating insulin level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0001262	decreased body weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10067829
MGI:3796418	M	MP:0001262	decreased body weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	F	MP:0001262	decreased body weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10974652
MGI:3796418	M	MP:0001258	decreased body length	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0001258	decreased body length	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10631109
MGI:3796418	M	MP:0006380	abnormal spermatid morphology	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12185100
MGI:3796418	M	MP:0002764	short tibia	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10631109
MGI:3796418	F	MP:0002293	long gestation period	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10342852
MGI:3796418	F	MP:0009019	abnormal metestrus	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	M	MP:0003402	decreased liver weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0031362	decreased prostate gland ventral lobe weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10067829
MGI:3796418	M	MP:0008975	delayed male fertility	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	M	MP:0002773	decreased circulating luteinizing hormone level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10067829
MGI:3796418	F	MP:0008976	delayed female fertility	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	9371826
MGI:3796418	M	MP:0003109	short femur	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10631109
MGI:3796418	M	MP:0003961	decreased lean body mass	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0001922	reduced male fertility	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10067829
MGI:3796418	F	MP:0004920	increased placenta weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10342852
MGI:3796418	M	MP:0003949	abnormal circulating lipid level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0004852	decreased testis weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12185100
MGI:3796418	M	MP:0004852	decreased testis weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10631109
MGI:3796418	M	MP:0004852	decreased testis weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10067829
MGI:3796418	M	MP:0002780	decreased circulating testosterone level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12185100
MGI:3796418	M	MP:0002780	decreased circulating testosterone level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10067829
MGI:3796418	M	MP:0002782	abnormal testes secretion	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12185100
MGI:3796418	M	MP:0001261	obese	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	F	MP:0004904	increased uterus weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10342852
MGI:3796418	M	MP:0004927	abnormal epididymis weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12185100
MGI:3796418	F	MP:0009011	prolonged diestrus	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	M	MP:0005124	increased circulating prolactin level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10067829
MGI:3796418	F	MP:0003355	decreased ovulation rate	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	M	MP:0005146	decreased circulating VLDL cholesterol level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0004929	decreased epididymis weight	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12185100
MGI:3796418	M	MP:0001156	abnormal spermatogenesis	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12185100
MGI:3796418	M	MP:0008271	abnormal bone ossification	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10631109
MGI:3796418	F	MP:0005560	decreased circulating glucose level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10974652
MGI:3796418	M	MP:0005560	decreased circulating glucose level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0005179	decreased circulating cholesterol level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0010124	decreased bone mineral content	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0001745	increased circulating corticosterone level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	F	MP:0001926	female infertility	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	F	MP:0005181	decreased circulating estradiol level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	F	MP:0003356	impaired luteinization	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	F	MP:0009006	prolonged estrous cycle	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	12297526
MGI:3796418	M	MP:0003797	abnormal compact bone morphology	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10631109
MGI:3796418	M	MP:0000183	decreased circulating LDL cholesterol level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	16174655
MGI:3796418	M	MP:0004686	decreased length of long bones	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10631109
MGI:3796418	M	MP:0004701	decreased circulating insulin-like growth factor I level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10067829
MGI:3796418	M	MP:0004701	decreased circulating insulin-like growth factor I level	Ghr<tm1Jjk>/Ghr<tm1Jjk>	involves: 129P2/OlaHsd * BALB/c	N	10631109
MGI:3796422	M	MP:0002169	no abnormal phenotype detected	Mirc2<tm1.1Tyj>/Y	involves: 129S4/SvJae * C57BL/6 * SJL	N	18329372
MGI:3796428	M	MP:0002169	no abnormal phenotype detected	Mirc2<tm1.1Tyj>/Y,Mirc3<tm1.1Tyj>/Mirc3<+>,Mirc1<tm1.2Tyj>/Mirc1<+>	involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL	N	18329372
MGI:3796444	M	MP:0002566	abnormal sexual interaction	Vegfa<tm2Pec>/Vegfa<tm2Pec>	involves: 129S1/Sv * 129X1/SvJ	N	11381259
MGI:3796444	F	MP:0001926	female infertility	Vegfa<tm2Pec>/Vegfa<tm2Pec>	involves: 129S1/Sv * 129X1/SvJ	N	11381259
MGI:3797141	M	MP:0001152	increased Leydig cell number	Patz1<tm1Pchi>/Patz1<tm1Pchi>	Not Specified	N	18241078
MGI:3797141	M	MP:0001153	small seminiferous tubules	Patz1<tm1Pchi>/Patz1<tm1Pchi>	Not Specified	N	18241078
MGI:3797141	M	MP:0001925	male infertility	Patz1<tm1Pchi>/Patz1<tm1Pchi>	Not Specified	N	18241078
MGI:3797141	M	MP:0002216	abnormal seminiferous tubule morphology	Patz1<tm1Pchi>/Patz1<tm1Pchi>	Not Specified	N	18241078
MGI:3797141	M	MP:0001147	small testis	Patz1<tm1Pchi>/Patz1<tm1Pchi>	Not Specified	N	18241078
MGI:3797141	M	MP:0005159	azoospermia	Patz1<tm1Pchi>/Patz1<tm1Pchi>	Not Specified	N	18241078
MGI:3797141	M	MP:0001155	arrest of spermatogenesis	Patz1<tm1Pchi>/Patz1<tm1Pchi>	Not Specified	N	18241078
MGI:3797141	M	MP:0002685	abnormal spermatogonia proliferation	Patz1<tm1Pchi>/Patz1<tm1Pchi>	Not Specified	N	18241078
MGI:3797141	F	MP:0001926	female infertility	Patz1<tm1Pchi>/Patz1<tm1Pchi>	Not Specified	N	18241078
MGI:3797141	M	MP:0004852	decreased testis weight	Patz1<tm1Pchi>/Patz1<tm1Pchi>	Not Specified	N	18241078
MGI:3797218	F	MP:0002169	no abnormal phenotype detected	S100g<tm1Ebje>/S100g<tm1Ebje>	involves: 129P2/OlaHsd	N	17696760
MGI:3797219	F	MP:0002904	increased circulating parathyroid hormone level	S100g<tm1Ebje>/S100g<tm1Ebje>,Del(6Ephb6-Trpv6)1Mhed/Del(6Ephb6-Trpv6)1Mhed	involves: 129P2/OlaHsd * 129S/SvEv	N	18325990
MGI:3797219	F	MP:0004231	abnormal calcium ion homeostasis	S100g<tm1Ebje>/S100g<tm1Ebje>,Del(6Ephb6-Trpv6)1Mhed/Del(6Ephb6-Trpv6)1Mhed	involves: 129P2/OlaHsd * 129S/SvEv	N	18325990
MGI:3797264	F	MP:0001923	reduced female fertility	Prkg1<tm2.1Naw>/Prkg1<tm2.1Naw>,Tagln<tm1(PRKG1*)Hfm>/Tagln<+>	involves: 129S1/Sv * 129X1/SvJ	N	17901360
MGI:3797265	F	MP:0001923	reduced female fertility	Prkg1<tm2.1Naw>/Prkg1<tm2.1Naw>,Tagln<tm2(PRKG1*)Hfm>/Tagln<+>	involves: 129S1/Sv * 129X1/SvJ	N	17901360
MGI:3797385	M	MP:0003666	impaired sperm capacitation	Cst8<tm1Itl>/Cst8<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	20811015
MGI:3797385	M	MP:0030978	impaired binding of sperm to zona pellucida	Cst8<tm1Itl>/Cst8<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	20811015
MGI:3797385	M	MP:0020451	decreased sperm progressive motility	Cst8<tm1Itl>/Cst8<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	20811015
MGI:3797385	M	MP:0004852	decreased testis weight	Cst8<tm1Itl>/Cst8<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	20811015
MGI:3797385	M	MP:0002675	asthenozoospermia	Cst8<tm1Itl>/Cst8<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	20811015
MGI:3797385	M	MP:0031009	abnormal sperm-egg fusion	Cst8<tm1Itl>/Cst8<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	20811015
MGI:3797385	M	MP:0004929	decreased epididymis weight	Cst8<tm1Itl>/Cst8<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	20811015
MGI:3797385	M	MP:0009647	decreased fertilization frequency	Cst8<tm1Itl>/Cst8<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	20811015
MGI:3797385	M	MP:0001156	abnormal spermatogenesis	Cst8<tm1Itl>/Cst8<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	20811015
MGI:3797385	M	MP:0004542	impaired acrosome reaction	Cst8<tm1Itl>/Cst8<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	20811015
MGI:3797385	M	MP:0002687	oligozoospermia	Cst8<tm1Itl>/Cst8<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	20811015
MGI:3797400	M	MP:0001922	reduced male fertility	Tekt4<tm1Zuk>/Tekt4<tm1Zuk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd	N	17244819
MGI:3797400	M	MP:0008892	abnormal sperm flagellum morphology	Tekt4<tm1Zuk>/Tekt4<tm1Zuk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd	N	17244819
MGI:3797400	M	MP:0030590	abnormal sperm fibrous sheath morphology	Tekt4<tm1Zuk>/Tekt4<tm1Zuk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd	N	17244819
MGI:3797400	M	MP:0009831	abnormal sperm midpiece morphology	Tekt4<tm1Zuk>/Tekt4<tm1Zuk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd	N	17244819
MGI:3797400	M	MP:0002675	asthenozoospermia	Tekt4<tm1Zuk>/Tekt4<tm1Zuk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd	N	17244819
MGI:3797400	M	MP:0004543	abnormal sperm physiology	Tekt4<tm1Zuk>/Tekt4<tm1Zuk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd	N	17244819
MGI:3797420	F	MP:0001134	absent corpus luteum	Cacnb4<lh>/Cacnb4<lh>	BALB/cGn-Cacnb4<lh>	N	MGI:60416
MGI:3797571	F	MP:0001134	absent corpus luteum	tb/tb	Not Specified	N	MGI:60416
MGI:3797572	F	MP:0001923	reduced female fertility	Cacna2d2<du-td>/Cacna2d2<du-td>	involves: DBA/2J	N	1195260
MGI:3797572	F	MP:0001134	absent corpus luteum	Cacna2d2<du-td>/Cacna2d2<du-td>	involves: DBA/2J	N	MGI:60416
MGI:3797724	F	MP:0008734	decreased susceptibility to endotoxin shock	Ikbkg<tm1Dwb>/Ikbkg<tm1Dwb>	Not Specified	N	18490708
MGI:3797724	F	MP:0008706	decreased interleukin-6 secretion	Ikbkg<tm1Dwb>/Ikbkg<tm1Dwb>	Not Specified	N	18490708
MGI:3797724	F	MP:0008722	abnormal chemokine secretion	Ikbkg<tm1Dwb>/Ikbkg<tm1Dwb>	Not Specified	N	18490708
MGI:3797724	F	MP:0001800	abnormal humoral immune response	Ikbkg<tm1Dwb>/Ikbkg<tm1Dwb>	Not Specified	N	18490708
MGI:3797724	F	MP:0008561	decreased tumor necrosis factor secretion	Ikbkg<tm1Dwb>/Ikbkg<tm1Dwb>	Not Specified	N	18490708
MGI:3797724	F	MP:0008670	decreased interleukin-12b secretion	Ikbkg<tm1Dwb>/Ikbkg<tm1Dwb>	Not Specified	N	18490708
MGI:3797747	F	MP:0011088	neonatal lethality, incomplete penetrance	Xlch/Xlch<+>	involves: C3H/HeJ * C57BL/6J	N	18424640
MGI:3797747	F	MP:0001625	cardiac hypertrophy	Xlch/Xlch<+>	involves: C3H/HeJ * C57BL/6J	N	18424640
MGI:3798055	F	MP:0009228	uterine cervix inflammation	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	N	16107615
MGI:3798055	F	MP:0001137	abnormal uterine cervix epithelium morphology	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	N	16107615
MGI:3798058	M	MP:0001922	reduced male fertility	Pip5k1b<tm1Tssk>/Pip5k1b<tm1Tssk>	involves: 129P2/OlaHsd	N	22321832
MGI:3798179	M	MP:0001402	decreased locomotor activity	Maoa<K284stop>/Y	129S6/SvEvTac-Maoa<K284stop>	N	18418249
MGI:3798179	M	MP:0001354	increased aggression towards male mice	Maoa<K284stop>/Y	129S6/SvEvTac-Maoa<K284stop>	N	18418249
MGI:3798180	F	MP:0002637	small uterus	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	N	18339713
MGI:3798180	F	MP:0008984	vagina hypoplasia	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	N	18339713
MGI:3798180	F	MP:0009371	increased theca cell number	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	N	18339713
MGI:3798180	F	MP:0001926	female infertility	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	N	18339713
MGI:3798180	F	MP:0009444	ovarian follicular cyst	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	N	18339713
MGI:3798180	F	MP:0000628	abnormal mammary gland development	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	N	18339713
MGI:3798180	F	MP:0001120	abnormal uterus morphology	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	N	18339713
MGI:3798180	F	MP:0001134	absent corpus luteum	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	N	18339713
MGI:3798180	F	MP:0001121	uterus hypoplasia	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	N	18339713
MGI:3798180	F	MP:0003357	impaired granulosa cell differentiation	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	N	18339713
MGI:3798180	F	MP:0001139	abnormal vagina morphology	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	N	18339713
MGI:3798180	F	MP:0011128	increased tertiary ovarian follicle number	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	N	18339713
MGI:3798180	F	MP:0008869	anovulation	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	N	18339713
MGI:3798199	F	MP:0001926	female infertility	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	N	12351685
MGI:3798199	F	MP:0009251	enlarged endometrial glands	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	N	12351685
MGI:3798199	F	MP:0009363	abnormal tertiary ovarian follicle morphology	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	N	12351685
MGI:3798199	F	MP:0004904	increased uterus weight	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	N	12351685
MGI:3798199	F	MP:0003355	decreased ovulation rate	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	N	12351685
MGI:3798199	F	MP:0009082	uterus cyst	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	N	12351685
MGI:3798199	F	MP:0001126	abnormal ovary morphology	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	N	12351685
MGI:3798199	F	MP:0004906	enlarged uterus	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	N	12351685
MGI:3798199	F	MP:0009671	abnormal uterus physiology	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	N	12351685
MGI:3798199	F	MP:0001134	absent corpus luteum	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	N	12351685
MGI:3798199	F	MP:0009092	endometrium hyperplasia	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	N	12351685
MGI:3798199	F	MP:0000662	abnormal branching of the mammary ductal tree	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	N	12351685
MGI:3798268	F	MP:0004904	increased uterus weight	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	N	16234973
MGI:3798269	F	MP:0004905	decreased uterus weight	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6	N	16234973
MGI:3798270	F	MP:0004905	decreased uterus weight	Esr1<tm1.1Lja>/Esr1<tm1.1Mma>	involves: 129P2/OlaHsd * 129S2/SvPas * 129X1/SvJ * C57BL/6	N	16234973
MGI:3798303	F	MP:0001134	absent corpus luteum	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798303	M	MP:0006416	abnormal rete testis morphology	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798303	F	MP:0031239	increased atretic ovarian follicle number	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798303	F	MP:0001126	abnormal ovary morphology	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798303	F	MP:0009009	absent estrous cycle	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798303	M	MP:0002216	abnormal seminiferous tubule morphology	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798303	F	MP:0001130	abnormal ovarian folliculogenesis	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798303	F	MP:0009444	ovarian follicular cyst	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798303	M	MP:0004901	decreased male germ cell number	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798303	F	MP:0001926	female infertility	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798303	F	MP:0008984	vagina hypoplasia	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798303	F	MP:0001121	uterus hypoplasia	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	F	MP:0001131	abnormal ovarian follicle morphology	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	M	MP:0004901	decreased male germ cell number	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	M	MP:0002784	abnormal Sertoli cell morphology	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	M	MP:0001925	male infertility	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	F	MP:0009444	ovarian follicular cyst	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	F	MP:0001121	uterus hypoplasia	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	F	MP:0001126	abnormal ovary morphology	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	M	MP:0006416	abnormal rete testis morphology	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	F	MP:0008984	vagina hypoplasia	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	F	MP:0008983	small vagina	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	F	MP:0009081	thin uterus	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	F	MP:0031239	increased atretic ovarian follicle number	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	F	MP:0003357	impaired granulosa cell differentiation	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	F	MP:0009363	abnormal tertiary ovarian follicle morphology	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	F	MP:0009370	decreased theca cell number	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798305	M	MP:0002216	abnormal seminiferous tubule morphology	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798306	F	MP:0001923	reduced female fertility	Esr1<tm1.1Mma>/Esr1<+>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798306	F	MP:0003357	impaired granulosa cell differentiation	Esr1<tm1.1Mma>/Esr1<+>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798306	F	MP:0001134	absent corpus luteum	Esr1<tm1.1Mma>/Esr1<+>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798306	F	MP:0011128	increased tertiary ovarian follicle number	Esr1<tm1.1Mma>/Esr1<+>,Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	N	10976058
MGI:3798307	F	MP:0002680	decreased corpora lutea number	Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas	N	10976058
MGI:3798307	F	MP:0001923	reduced female fertility	Esr2<tm1Mma>/Esr2<tm1Mma>	involves: 129S2/SvPas	N	10976058
MGI:3798388	F	MP:0001927	abnormal estrous cycle	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cga-cre)3Sac/0	involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL	N	17947360
MGI:3798388	F	MP:0001926	female infertility	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cga-cre)3Sac/0	involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL	N	17947360
MGI:3798388	F	MP:0009444	ovarian follicular cyst	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cga-cre)3Sac/0	involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL	N	17947360
MGI:3798408	F	MP:0002680	decreased corpora lutea number	Esr2<tm1.2Pcn>/Esr2<tm1.2Pcn>	involves: 129S2/SvPas * C57BL/6 * SJL	N	18268329
MGI:3798408	F	MP:0031422	failure of superovulation	Esr2<tm1.2Pcn>/Esr2<tm1.2Pcn>	involves: 129S2/SvPas * C57BL/6 * SJL	N	18268329
MGI:3798408	F	MP:0001926	female infertility	Esr2<tm1.2Pcn>/Esr2<tm1.2Pcn>	involves: 129S2/SvPas * C57BL/6 * SJL	N	18268329
MGI:3798408	F	MP:0001927	abnormal estrous cycle	Esr2<tm1.2Pcn>/Esr2<tm1.2Pcn>	involves: 129S2/SvPas * C57BL/6 * SJL	N	18268329
MGI:3798408	F	MP:0031239	increased atretic ovarian follicle number	Esr2<tm1.2Pcn>/Esr2<tm1.2Pcn>	involves: 129S2/SvPas * C57BL/6 * SJL	N	18268329
MGI:3798408	M	MP:0001925	male infertility	Esr2<tm1.2Pcn>/Esr2<tm1.2Pcn>	involves: 129S2/SvPas * C57BL/6 * SJL	N	18268329
MGI:3798457	F	MP:0000352	decreased cell proliferation	Hs6st1<tm1Kkm>/Hs6st1<tm1Kkm>,Hs6st2<tm1.1Kkm>/Hs6st2<tm1.1Kkm>	involves: 129P2/OlaHsd	N	18281280
MGI:3798605	M	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx-2Cv>/Y	involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	N	2919177
MGI:3798605	M	MP:0003141	cardiac fibrosis	Dmd<mdx-2Cv>/Y	involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	N	2919177
MGI:3798605	M	MP:0009412	skeletal muscle fiber degeneration	Dmd<mdx-2Cv>/Y	involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	N	2919177
MGI:3798605	M	MP:0003157	impaired muscle relaxation	Dmd<mdx-2Cv>/Y	involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	N	2919177
MGI:3798606	M	MP:0009412	skeletal muscle fiber degeneration	Dmd<mdx-3Cv>/Y	involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	N	2919177
MGI:3798606	M	MP:0003157	impaired muscle relaxation	Dmd<mdx-3Cv>/Y	involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	N	2919177
MGI:3798606	M	MP:0003141	cardiac fibrosis	Dmd<mdx-3Cv>/Y	involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	N	2919177
MGI:3798606	M	MP:0005551	abnormal eye electrophysiology	Dmd<mdx-3Cv>/Y	involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	N	7843915
MGI:3798607	M	MP:0009414	skeletal muscle fiber necrosis	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	3440862
MGI:3798607	M	MP:0001262	decreased body weight	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	21893021
MGI:3798607	M	MP:0030957	abnormal myotube morphology	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:3798607	M	MP:0004566	myocardial fiber degeneration	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	2919177
MGI:3798607	M	MP:0014143	decreased body fat mass	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	21893021
MGI:3798607	M	MP:0005386	behavior/neurological phenotype	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	Y	21893021
MGI:3798607	M	MP:0002899	fatigue	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	21893021
MGI:3798607	M	MP:0000278	abnormal myocardial fiber morphology	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:3798607	M	MP:0009419	skeletal muscle fibrosis	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	21893021
MGI:3798607	M	MP:0010053	decreased grip strength	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	21893021
MGI:3798607	M	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:3798607	M	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	3440862
MGI:3798607	M	MP:0002953	thick ventricular wall	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:3798607	M	MP:0005620	abnormal muscle contractility	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	3440862
MGI:3798607	M	MP:0002280	abnormal intercostal muscle morphology	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:3798607	M	MP:0001407	short stride length	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	21893021
MGI:3798607	M	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	3440862
MGI:3798607	M	MP:0005369	muscle phenotype	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	Y	21893021
MGI:3798607	M	MP:0009412	skeletal muscle fiber degeneration	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	2919177
MGI:3798607	M	MP:0001406	abnormal gait	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	21893021
MGI:3798607	M	MP:0000733	abnormal muscle development	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:3798607	M	MP:0003157	impaired muscle relaxation	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	2919177
MGI:3798607	M	MP:0003105	abnormal heart atrium morphology	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:3798607	M	MP:0002841	impaired skeletal muscle contractility	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	21893021
MGI:3798607	M	MP:0010581	abnormal atrium myocardial trabeculae morphology	Dmd<mdx>/Y	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:3798614	F	MP:0009419	skeletal muscle fibrosis	Dmd<mdx-2Cv>/Dmd<mdx-2Cv>	B6Ros.Cg-Dmd<mdx-2Cv>	N	1635838
MGI:3798614	F	MP:0002279	abnormal diaphragm morphology	Dmd<mdx-2Cv>/Dmd<mdx-2Cv>	B6Ros.Cg-Dmd<mdx-2Cv>	N	1635838
MGI:3798615	M	MP:0009419	skeletal muscle fibrosis	Dmd<mdx-2Cv>/Y	B6Ros.Cg-Dmd<mdx-2Cv>	N	1635838
MGI:3798615	M	MP:0002279	abnormal diaphragm morphology	Dmd<mdx-2Cv>/Y	B6Ros.Cg-Dmd<mdx-2Cv>	N	1635838
MGI:3798616	F	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>	B6Ros.Cg-Dmd<mdx-3Cv>	N	1635838
MGI:3798616	F	MP:0009403	increased variability of skeletal muscle fiber size	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>	B6Ros.Cg-Dmd<mdx-3Cv>	N	8099842
MGI:3798616	F	MP:0011110	preweaning lethality, incomplete penetrance	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>	B6Ros.Cg-Dmd<mdx-3Cv>	N	8099842
MGI:3798616	F	MP:0009419	skeletal muscle fibrosis	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>	B6Ros.Cg-Dmd<mdx-3Cv>	N	1635838
MGI:3798616	F	MP:0001921	reduced fertility	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>	B6Ros.Cg-Dmd<mdx-3Cv>	N	8099842
MGI:3798616	F	MP:0002279	abnormal diaphragm morphology	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>	B6Ros.Cg-Dmd<mdx-3Cv>	N	1635838
MGI:3798616	F	MP:0001935	decreased litter size	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>	B6Ros.Cg-Dmd<mdx-3Cv>	N	8099842
MGI:3798617	M	MP:0002279	abnormal diaphragm morphology	Dmd<mdx-3Cv>/Y	B6Ros.Cg-Dmd<mdx-3Cv>	N	1635838
MGI:3798617	M	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx-3Cv>/Y	B6Ros.Cg-Dmd<mdx-3Cv>	N	1635838
MGI:3798617	M	MP:0001921	reduced fertility	Dmd<mdx-3Cv>/Y	B6Ros.Cg-Dmd<mdx-3Cv>	N	8099842
MGI:3798617	M	MP:0001935	decreased litter size	Dmd<mdx-3Cv>/Y	B6Ros.Cg-Dmd<mdx-3Cv>	N	8099842
MGI:3798617	M	MP:0009403	increased variability of skeletal muscle fiber size	Dmd<mdx-3Cv>/Y	B6Ros.Cg-Dmd<mdx-3Cv>	N	8099842
MGI:3798617	M	MP:0011110	preweaning lethality, incomplete penetrance	Dmd<mdx-3Cv>/Y	B6Ros.Cg-Dmd<mdx-3Cv>	N	8099842
MGI:3798617	M	MP:0009419	skeletal muscle fibrosis	Dmd<mdx-3Cv>/Y	B6Ros.Cg-Dmd<mdx-3Cv>	N	1635838
MGI:3798618	F	MP:0002279	abnormal diaphragm morphology	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>	B6Ros.Cg-Dmd<mdx-4Cv>	N	1635838
MGI:3798618	F	MP:0009419	skeletal muscle fibrosis	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>	B6Ros.Cg-Dmd<mdx-4Cv>	N	1635838
MGI:3798619	M	MP:0009419	skeletal muscle fibrosis	Dmd<mdx-4Cv>/Y	B6Ros.Cg-Dmd<mdx-4Cv>	N	1635838
MGI:3798619	M	MP:0002279	abnormal diaphragm morphology	Dmd<mdx-4Cv>/Y	B6Ros.Cg-Dmd<mdx-4Cv>	N	1635838
MGI:3798620	F	MP:0002279	abnormal diaphragm morphology	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>	B6Ros.Cg-Dmd<mdx-5Cv>	N	1635838
MGI:3798620	F	MP:0009419	skeletal muscle fibrosis	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>	B6Ros.Cg-Dmd<mdx-5Cv>	N	1635838
MGI:3798621	M	MP:0002899	fatigue	Dmd<mdx-5Cv>/Y	B6Ros.Cg-Dmd<mdx-5Cv>	N	21893021
MGI:3798621	M	MP:0002279	abnormal diaphragm morphology	Dmd<mdx-5Cv>/Y	B6Ros.Cg-Dmd<mdx-5Cv>	N	1635838
MGI:3798621	M	MP:0005369	muscle phenotype	Dmd<mdx-5Cv>/Y	B6Ros.Cg-Dmd<mdx-5Cv>	Y	21893021
MGI:3798621	M	MP:0001262	decreased body weight	Dmd<mdx-5Cv>/Y	B6Ros.Cg-Dmd<mdx-5Cv>	N	21893021
MGI:3798621	M	MP:0002841	impaired skeletal muscle contractility	Dmd<mdx-5Cv>/Y	B6Ros.Cg-Dmd<mdx-5Cv>	N	21893021
MGI:3798621	M	MP:0010053	decreased grip strength	Dmd<mdx-5Cv>/Y	B6Ros.Cg-Dmd<mdx-5Cv>	N	21893021
MGI:3798621	M	MP:0009419	skeletal muscle fibrosis	Dmd<mdx-5Cv>/Y	B6Ros.Cg-Dmd<mdx-5Cv>	N	1635838
MGI:3798621	M	MP:0014143	decreased body fat mass	Dmd<mdx-5Cv>/Y	B6Ros.Cg-Dmd<mdx-5Cv>	N	21893021
MGI:3798621	M	MP:0009419	skeletal muscle fibrosis	Dmd<mdx-5Cv>/Y	B6Ros.Cg-Dmd<mdx-5Cv>	N	21893021
MGI:3798621	M	MP:0001406	abnormal gait	Dmd<mdx-5Cv>/Y	B6Ros.Cg-Dmd<mdx-5Cv>	N	21893021
MGI:3798621	M	MP:0001407	short stride length	Dmd<mdx-5Cv>/Y	B6Ros.Cg-Dmd<mdx-5Cv>	N	21893021
MGI:3798621	M	MP:0001405	impaired coordination	Dmd<mdx-5Cv>/Y	B6Ros.Cg-Dmd<mdx-5Cv>	N	21893021
MGI:3798621	M	MP:0003646	increased muscle fatigability	Dmd<mdx-5Cv>/Y	B6Ros.Cg-Dmd<mdx-5Cv>	N	21893021
MGI:3798630	M	MP:0005551	abnormal eye electrophysiology	Dmd<mdx-2Cv>/Y	B6Ros.Cg-Dmd<mdx-2Cv>/J	N	10068512
MGI:3798631	F	MP:0005547	abnormal Muller cell morphology	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>	B6.Cg-Dmd<mdx-3Cv>/J	N	12040037
MGI:3798632	M	MP:0009403	increased variability of skeletal muscle fiber size	Dmd<mdx-3Cv>/Y	B6.Cg-Dmd<mdx-3Cv>/J	N	18385524
MGI:3798632	M	MP:0005551	abnormal eye electrophysiology	Dmd<mdx-3Cv>/Y	B6.Cg-Dmd<mdx-3Cv>/J	N	10068512
MGI:3798632	M	MP:0001515	abnormal grip strength	Dmd<mdx-3Cv>/Y	B6.Cg-Dmd<mdx-3Cv>/J	N	18385524
MGI:3798632	M	MP:0005391	vision/eye phenotype	Dmd<mdx-3Cv>/Y	B6.Cg-Dmd<mdx-3Cv>/J	Y	10068512
MGI:3798632	M	MP:0005547	abnormal Muller cell morphology	Dmd<mdx-3Cv>/Y	B6.Cg-Dmd<mdx-3Cv>/J	N	12040037
MGI:3798632	M	MP:0005620	abnormal muscle contractility	Dmd<mdx-3Cv>/Y	B6.Cg-Dmd<mdx-3Cv>/J	N	18385524
MGI:3798632	M	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx-3Cv>/Y	B6.Cg-Dmd<mdx-3Cv>/J	N	18385524
MGI:3798632	M	MP:0000759	abnormal skeletal muscle morphology	Dmd<mdx-3Cv>/Y	B6.Cg-Dmd<mdx-3Cv>/J	N	18385524
MGI:3798634	M	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx-4Cv>/Y	B6Ros.Cg-Dmd<mdx-4Cv>/J	N	18385524
MGI:3798634	M	MP:0005551	abnormal eye electrophysiology	Dmd<mdx-4Cv>/Y	B6Ros.Cg-Dmd<mdx-4Cv>/J	N	10068512
MGI:3798634	M	MP:0005620	abnormal muscle contractility	Dmd<mdx-4Cv>/Y	B6Ros.Cg-Dmd<mdx-4Cv>/J	N	18385524
MGI:3798634	M	MP:0001515	abnormal grip strength	Dmd<mdx-4Cv>/Y	B6Ros.Cg-Dmd<mdx-4Cv>/J	N	18385524
MGI:3798634	M	MP:0000759	abnormal skeletal muscle morphology	Dmd<mdx-4Cv>/Y	B6Ros.Cg-Dmd<mdx-4Cv>/J	N	18385524
MGI:3798634	M	MP:0009403	increased variability of skeletal muscle fiber size	Dmd<mdx-4Cv>/Y	B6Ros.Cg-Dmd<mdx-4Cv>/J	N	18385524
MGI:3798662	F	MP:0003631	nervous system phenotype	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	Y	10204788
MGI:3798662	F	MP:0005367	renal/urinary system phenotype	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	Y	10204788
MGI:3798662	F	MP:0005370	liver/biliary system phenotype	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	Y	10204788
MGI:3798662	F	MP:0005388	respiratory system phenotype	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	Y	10204788
MGI:3798662	F	MP:0000759	abnormal skeletal muscle morphology	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	N	10204788
MGI:3798662	F	MP:0005389	reproductive system phenotype	Dmd<mdx-3Cv>/Dmd<mdx-3Cv>,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	Y	10204788
MGI:3798665	M	MP:0005367	renal/urinary system phenotype	Dmd<mdx-3Cv>/Y,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	Y	10204788
MGI:3798665	M	MP:0005370	liver/biliary system phenotype	Dmd<mdx-3Cv>/Y,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	Y	10204788
MGI:3798665	M	MP:0000759	abnormal skeletal muscle morphology	Dmd<mdx-3Cv>/Y,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	N	10204788
MGI:3798665	M	MP:0003631	nervous system phenotype	Dmd<mdx-3Cv>/Y,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	Y	10204788
MGI:3798665	M	MP:0005388	respiratory system phenotype	Dmd<mdx-3Cv>/Y,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	Y	10204788
MGI:3798665	M	MP:0005389	reproductive system phenotype	Dmd<mdx-3Cv>/Y,Utrn<tm1Ked>/Utrn<tm1Ked>	involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	Y	10204788
MGI:3798777	F	MP:0009414	skeletal muscle fiber necrosis	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>	involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	N	17961534
MGI:3798777	F	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>	involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	N	17961534
MGI:3798777	F	MP:0000730	increased satellite cell number	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>	involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	N	17961534
MGI:3798777	F	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>	involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	N	17961534
MGI:3798778	F	MP:0009414	skeletal muscle fiber necrosis	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Myf5<tm2Tajb>/Myf5<tm2Tajb>	involves: 129S2/SvPas * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	N	17961534
MGI:3798778	F	MP:0009401	increased skeletal muscle fiber diameter	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Myf5<tm2Tajb>/Myf5<tm2Tajb>	involves: 129S2/SvPas * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	N	17961534
MGI:3798788	F	MP:0004215	abnormal myocardial fiber physiology	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>	B6Ros.Cg-Dmd<mdx-5Cv>/J	N	16857961
MGI:3798788	F	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>	B6Ros.Cg-Dmd<mdx-5Cv>/J	N	20705734
MGI:3798788	F	MP:0005620	abnormal muscle contractility	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>	B6Ros.Cg-Dmd<mdx-5Cv>/J	N	20705734
MGI:3798788	F	MP:0009403	increased variability of skeletal muscle fiber size	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>	B6Ros.Cg-Dmd<mdx-5Cv>/J	N	20705734
MGI:3798788	F	MP:0000730	increased satellite cell number	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>	B6Ros.Cg-Dmd<mdx-5Cv>/J	N	20705734
MGI:3798788	F	MP:0004071	prolonged P wave	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>	B6Ros.Cg-Dmd<mdx-5Cv>/J	N	16857961
MGI:3798788	F	MP:0010509	decreased P wave amplitude	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>	B6Ros.Cg-Dmd<mdx-5Cv>/J	N	16857961
MGI:3798788	F	MP:0010392	prolonged QRS complex duration	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>	B6Ros.Cg-Dmd<mdx-5Cv>/J	N	16857961
MGI:3798788	F	MP:0005385	cardiovascular system phenotype	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>	B6Ros.Cg-Dmd<mdx-5Cv>/J	Y	16857961
MGI:3798791	F	MP:0006190	retina ischemia	Dmd<tm1Ndl>/Dmd<tm1Ndl>	involves: 129S1/Sv * 129X1/SvJ	N	12812982
MGI:3798917	F	MP:0009097	absent endometrial glands	Tg(CD3E)26Cpt/Tg(CD3E)26Cpt	involves: C57BL/6J * CBA/J	N	9002646
MGI:3798917	F	MP:0004896	abnormal endometrium morphology	Tg(CD3E)26Cpt/Tg(CD3E)26Cpt	involves: C57BL/6J * CBA/J	N	9002646
MGI:3798917	F	MP:0001120	abnormal uterus morphology	Tg(CD3E)26Cpt/Tg(CD3E)26Cpt	involves: C57BL/6J * CBA/J	N	9002646
MGI:3798917	F	MP:0008876	decreased uterine NK cell number	Tg(CD3E)26Cpt/Tg(CD3E)26Cpt	involves: C57BL/6J * CBA/J	N	9002646
MGI:3798924	F	MP:0001545	abnormal hematopoietic system physiology	Gata1<tm2.1Sho>/Gata1<tm2.1Sho>	involves: 129/Sv * 129S4/SvJae	N	9716588
MGI:3798925	F	MP:0010878	increased trabecular bone volume	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae	N	15005853
MGI:3798925	F	MP:0004988	increased osteoblast cell number	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae	N	15005853
MGI:3798925	F	MP:0004984	increased osteoclast cell number	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae	N	15005853
MGI:3798925	F	MP:0010964	increased compact bone volume	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae	N	15005853
MGI:3798925	F	MP:0020039	increased bone ossification	Gata1<tm2Sho>/Gata1<tm2Sho>	involves: 129S4/SvJae	N	15005853
MGI:3798942	F	MP:0004896	abnormal endometrium morphology	Il2rb<tm1Mak>/Il2rb<tm1Mak>,Lck<tm1Mak>/Lck<tm1Mak>	involves: 129	N	9002646
MGI:3798942	F	MP:0008047	absent uterine NK cells	Il2rb<tm1Mak>/Il2rb<tm1Mak>,Lck<tm1Mak>/Lck<tm1Mak>	involves: 129	N	9002646
MGI:3798942	F	MP:0004256	abnormal maternal decidual layer morphology	Il2rb<tm1Mak>/Il2rb<tm1Mak>,Lck<tm1Mak>/Lck<tm1Mak>	involves: 129	N	9002646
MGI:3798942	F	MP:0009097	absent endometrial glands	Il2rb<tm1Mak>/Il2rb<tm1Mak>,Lck<tm1Mak>/Lck<tm1Mak>	involves: 129	N	9002646
MGI:3799265	M	MP:0005169	abnormal male meiosis	Tex11<tm1.1Jpt>/Y	involves: 129/Sv * C57BL/6 * CD-1	N	18369460
MGI:3799265	M	MP:0005389	reproductive system phenotype	Tex11<tm1.1Jpt>/Y	involves: 129/Sv * C57BL/6 * CD-1	Y	18369460
MGI:3799265	M	MP:0001156	abnormal spermatogenesis	Tex11<tm1.1Jpt>/Y	involves: 129/Sv * C57BL/6 * CD-1	N	18369460
MGI:3799268	F	MP:0008978	abnormal vagina weight	Fas<lpr>/Fas<lpr>	C3.MRL-Fas<lpr>	N	10453074
MGI:3799457	F	MP:0006270	abnormal mammary gland growth during lactation	Tg(Trp53R172L)4491Jmr/0	FVB/N-Tg(Trp53R172L)4491Jmr	N	7947386
MGI:3799457	F	MP:0010249	lactation failure	Tg(Trp53R172L)4491Jmr/0	FVB/N-Tg(Trp53R172L)4491Jmr	N	7947386
MGI:3799457	F	MP:0001881	abnormal mammary gland physiology	Tg(Trp53R172L)4491Jmr/0	FVB/N-Tg(Trp53R172L)4491Jmr	N	7947386
MGI:3799464	F	MP:0006270	abnormal mammary gland growth during lactation	Tg(Trp53R172L)4491Jmr/0	involves: FVB/N	N	7576102
MGI:3799537	M	MP:0001925	male infertility	Vsx2<or-2J>/Vsx2<or-2J>	NOR2/LtDn-Vsx2<or-2J>/J	N	MGI:78457
MGI:3799537	F	MP:0001926	female infertility	Vsx2<or-2J>/Vsx2<or-2J>	NOR2/LtDn-Vsx2<or-2J>/J	N	MGI:78457
MGI:3799623	M	MP:0002115	abnormal limb bone morphology	Atp7a<Mo-dp>/Y	Not Specified	N	MGI:61157
MGI:3799623	M	MP:0004509	abnormal pelvic girdle bone morphology	Atp7a<Mo-dp>/Y	Not Specified	N	MGI:61157
MGI:3799623	M	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance	Atp7a<Mo-dp>/Y	Not Specified	N	MGI:61157
MGI:3799623	M	MP:0000150	abnormal rib morphology	Atp7a<Mo-dp>/Y	Not Specified	N	MGI:61157
MGI:3799623	M	MP:0004676	wide ribs	Atp7a<Mo-dp>/Y	Not Specified	N	MGI:61157
MGI:3799623	M	MP:0011089	perinatal lethality, complete penetrance	Atp7a<Mo-dp>/Y	Not Specified	N	MGI:61157
MGI:3799623	M	MP:0004508	abnormal pectoral girdle bone morphology	Atp7a<Mo-dp>/Y	Not Specified	N	MGI:61157
MGI:3799643	F	MP:0000628	abnormal mammary gland development	Tg(MtTGFA)42Lmb/Tg(MtTGFA)42Lmb	involves: CD-1	N	2350785
MGI:3799681	F	MP:0005397	hematopoietic system phenotype	Tlr7<tm1Aki>/Tlr7<tm1Aki>	involves: 129P2/OlaHsd * C57BL/6	Y	18492657
MGI:3800167	F	MP:0006271	abnormal involution of the mammary gland	Tg(MtTGFA)100Lmb/0	involves: FVB/N	N	7573353
MGI:3800167	F	MP:0000627	abnormal mammary gland morphology	Tg(MtTGFA)100Lmb/0	involves: FVB/N	N	7573353
MGI:3800194	M	MP:0001147	small testis	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	16427009
MGI:3800194	M	MP:0002687	oligozoospermia	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	16427009
MGI:3800194	M	MP:0001153	small seminiferous tubules	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	16427009
MGI:3800194	M	MP:0001925	male infertility	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	16427009
MGI:3800198	F	MP:0000630	mammary gland hyperplasia	Tg(MMTVTGFA)254Rjc/0	involves: C57BL/6 * DBA/2	N	1316084
MGI:3800198	F	MP:0001382	abnormal nursing	Tg(MMTVTGFA)254Rjc/0	involves: C57BL/6 * DBA/2	N	1316084
MGI:3800199	F	MP:0000630	mammary gland hyperplasia	Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2	N	7753792
MGI:3800199	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2	N	2161707
MGI:3800199	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2	N	1316084
MGI:3800199	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2	N	1316084
MGI:3800199	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2	N	2161707
MGI:3800199	F	MP:0001382	abnormal nursing	Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2	N	1316084
MGI:3800199	F	MP:0006269	abnormal mammary gland growth during pregnancy	Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2	N	2161707
MGI:3800199	F	MP:0001885	mammary gland duct hyperplasia	Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2	N	2161707
MGI:3800199	F	MP:0006269	abnormal mammary gland growth during pregnancy	Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2	N	1316084
MGI:3800199	F	MP:0000630	mammary gland hyperplasia	Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2	N	8816486
MGI:3800199	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2	N	8816486
MGI:3800199	F	MP:0001382	abnormal nursing	Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2	N	2161707
MGI:3800199	F	MP:0009506	abnormal mammary gland alveolus morphology	Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2	N	8816486
MGI:3800200	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTVTGFA)64Rjc/0	involves: C57BL/6 * DBA/2	N	1316084
MGI:3800200	F	MP:0001382	abnormal nursing	Tg(MMTVTGFA)64Rjc/0	involves: C57BL/6 * DBA/2	N	1316084
MGI:3800200	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTVTGFA)64Rjc/0	involves: C57BL/6 * DBA/2	N	2161707
MGI:3800230	F	MP:0009505	abnormal mammary gland lobule morphology	Tg(MMTVTGFB1)46Hlm/0	involves: C57BL/6 * DBA/2	N	8253379
MGI:3800230	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(MMTVTGFB1)46Hlm/0	involves: C57BL/6 * DBA/2	N	8253379
MGI:3800230	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTVTGFB1)46Hlm/0	involves: C57BL/6 * DBA/2	N	8253379
MGI:3800230	F	MP:0013781	abnormal mammary gland luminal epithelium morphology	Tg(MMTVTGFB1)46Hlm/0	involves: C57BL/6 * DBA/2	N	8253379
MGI:3800230	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(MMTVTGFB1)46Hlm/0	involves: C57BL/6 * DBA/2	N	7753792
MGI:3800237	M	MP:0001147	small testis	Rnf8<Gt(RRR260)Byg>/Rnf8<Gt(RRR260)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:3800237	M	MP:0006378	abnormal spermatogonia morphology	Rnf8<Gt(RRR260)Byg>/Rnf8<Gt(RRR260)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:3800237	M	MP:0001925	male infertility	Rnf8<Gt(RRR260)Byg>/Rnf8<Gt(RRR260)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:3800237	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Rnf8<Gt(RRR260)Byg>/Rnf8<Gt(RRR260)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:3800237	M	MP:0002687	oligozoospermia	Rnf8<Gt(RRR260)Byg>/Rnf8<Gt(RRR260)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:3800237	M	MP:0001156	abnormal spermatogenesis	Rnf8<Gt(RRR260)Byg>/Rnf8<Gt(RRR260)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:3800237	M	MP:0006379	abnormal spermatocyte morphology	Rnf8<Gt(RRR260)Byg>/Rnf8<Gt(RRR260)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:3800237	M	MP:0005159	azoospermia	Rnf8<Gt(RRR260)Byg>/Rnf8<Gt(RRR260)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:3800237	M	MP:0001154	seminiferous tubule degeneration	Rnf8<Gt(RRR260)Byg>/Rnf8<Gt(RRR260)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:3800247	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(MMTVTGFA)29Rjc/0,Tg(MMTVTGFB1)46Hlm/0	involves: C57BL/6 * DBA/2	N	7753792
MGI:3800286	F	MP:0000630	mammary gland hyperplasia	Tg(MMTVneu)202Mul/0,Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2 * FVB/N	N	8816486
MGI:3800286	F	MP:0001382	abnormal nursing	Tg(MMTVneu)202Mul/0,Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2 * FVB/N	N	8816486
MGI:3800286	F	MP:0009503	abnormal mammary gland duct morphology	Tg(MMTVneu)202Mul/0,Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2 * FVB/N	N	8816486
MGI:3800286	F	MP:0009506	abnormal mammary gland alveolus morphology	Tg(MMTVneu)202Mul/0,Tg(MMTVTGFA)29Rjc/0	involves: C57BL/6 * DBA/2 * FVB/N	N	8816486
MGI:3800494	M	MP:0001925	male infertility	Sptbn4<qv-10J>/Sptbn4<qv-10J>	involves: BALB/cJ * C57BL/6J	N	MGI:3799697
MGI:3800580	M	MP:0001925	male infertility	ocd/ocd	C3H/HeSnJ-ocd	N	2013688
MGI:3800604	F	MP:0001923	reduced female fertility	nr/nr	BALB/cGr-nr	N	MGI:63062
MGI:3800604	M	MP:0001922	reduced male fertility	nr/nr	BALB/cGr-nr	N	MGI:63062
MGI:3800637	F	MP:0006271	abnormal involution of the mammary gland	Tg(WapIGFBP3)67Dlr/0	involves: C57BL/6 * SJL	N	8636401
MGI:3800637	F	MP:0009506	abnormal mammary gland alveolus morphology	Tg(WapIGFBP3)67Dlr/0	involves: C57BL/6 * SJL	N	8636401
MGI:3800637	F	MP:0001885	mammary gland duct hyperplasia	Tg(WapIGFBP3)67Dlr/0	involves: C57BL/6 * SJL	N	8817687
MGI:3800638	F	MP:0006271	abnormal involution of the mammary gland	Tg(WapIgf1)39Dlr/0	involves: C57BL/6 * SJL	N	8636401
MGI:3800638	F	MP:0006271	abnormal involution of the mammary gland	Tg(WapIgf1)39Dlr/0	involves: C57BL/6 * SJL	N	8817687
MGI:3800638	F	MP:0009506	abnormal mammary gland alveolus morphology	Tg(WapIgf1)39Dlr/0	involves: C57BL/6 * SJL	N	8636401
MGI:3800638	F	MP:0001885	mammary gland duct hyperplasia	Tg(WapIgf1)39Dlr/0	involves: C57BL/6 * SJL	N	8636401
MGI:3800654	M	MP:0003666	impaired sperm capacitation	Pkdrej<tm1Dgen>/Pkdrej<tm1Dgen>	B6.Cg-Pkdrej<tm1Dgen>	N	18562295
MGI:3800659	F	MP:0009505	abnormal mammary gland lobule morphology	Tg(WapMyc)212Bri/0	FVB.Cg-Tg(WapMyc)212Bri	N	17071603
MGI:3800659	F	MP:0001885	mammary gland duct hyperplasia	Tg(WapMyc)212Bri/0	FVB.Cg-Tg(WapMyc)212Bri	N	17071603
MGI:3800659	F	MP:0000630	mammary gland hyperplasia	Tg(WapMyc)212Bri/0	FVB.Cg-Tg(WapMyc)212Bri	N	17071603
MGI:3800659	F	MP:0000627	abnormal mammary gland morphology	Tg(WapMyc)212Bri/0	FVB.Cg-Tg(WapMyc)212Bri	N	17071603
MGI:3800660	F	MP:0000630	mammary gland hyperplasia	Tg(Mt1-Tgfa)147Bri/0	involves: C57BL/6 * SJL	N	7641211
MGI:3800660	F	MP:0006271	abnormal involution of the mammary gland	Tg(Mt1-Tgfa)147Bri/0	involves: C57BL/6 * SJL	N	7641211
MGI:3800661	F	MP:0000630	mammary gland hyperplasia	Tg(WapTgfa)215Bri/0	FVB.Cg-Tg(WapTgfa)215Bri	N	17071603
MGI:3800661	F	MP:0000627	abnormal mammary gland morphology	Tg(WapTgfa)215Bri/0	FVB.Cg-Tg(WapTgfa)215Bri	N	17071603
MGI:3800661	F	MP:0009505	abnormal mammary gland lobule morphology	Tg(WapTgfa)215Bri/0	FVB.Cg-Tg(WapTgfa)215Bri	N	17071603
MGI:3800661	F	MP:0001885	mammary gland duct hyperplasia	Tg(WapTgfa)215Bri/0	FVB.Cg-Tg(WapTgfa)215Bri	N	17071603
MGI:3800662	F	MP:0000630	mammary gland hyperplasia	Tg(WapMyc)212Bri/0,Tg(WapTgfa)215Bri/0	involves: C57BL/6 * SJL	N	7641211
MGI:3800662	F	MP:0006271	abnormal involution of the mammary gland	Tg(WapMyc)212Bri/0,Tg(WapTgfa)215Bri/0	involves: C57BL/6 * SJL	N	7641211
MGI:3800662	F	MP:0001882	abnormal lactation	Tg(WapMyc)212Bri/0,Tg(WapTgfa)215Bri/0	involves: C57BL/6 * SJL	N	7641211
MGI:3800787	F	MP:0009011	prolonged diestrus	Akr1c18<tm1Mni>/Akr1c18<tm1Mni>	involves: 129P2/OlaHsd * C57BL/6J	N	17272929
MGI:3800787	F	MP:0009006	prolonged estrous cycle	Akr1c18<tm1Mni>/Akr1c18<tm1Mni>	involves: 129P2/OlaHsd * C57BL/6J	N	17272929
MGI:3800787	F	MP:0002293	long gestation period	Akr1c18<tm1Mni>/Akr1c18<tm1Mni>	involves: 129P2/OlaHsd * C57BL/6J	N	17272929
MGI:3800802	F	MP:0010249	lactation failure	Tg(WapMyc)212Bri/0	involves: C57BL/6 * SJL	N	7641211
MGI:3800802	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(WapMyc)212Bri/0	involves: C57BL/6 * SJL	N	7641211
MGI:3800803	F	MP:0010249	lactation failure	Tg(WapTgfa)215Bri/0	involves: C57BL/6 * SJL	N	7641211
MGI:3800803	F	MP:0006269	abnormal mammary gland growth during pregnancy	Tg(WapTgfa)215Bri/0	involves: C57BL/6 * SJL	N	7641211
MGI:3800803	F	MP:0000630	mammary gland hyperplasia	Tg(WapTgfa)215Bri/0	involves: C57BL/6 * SJL	N	7641211
MGI:3800803	F	MP:0006271	abnormal involution of the mammary gland	Tg(WapTgfa)215Bri/0	involves: C57BL/6 * SJL	N	7641211
MGI:3800804	F	MP:0000630	mammary gland hyperplasia	Muc1<tm1Gend>/Muc1<tm1Gend>,Tg(WapTgfa)215Bri/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17638868
MGI:3800805	F	MP:0000630	mammary gland hyperplasia	Tg(WapTgfa)215Bri/0	B6.Cg-Tg(WapTgfa)215Bri	N	17638868
MGI:3800807	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(MtTPRMET)243Lng/0	FVB/N-Tg(MtTPRMET)243Lng	N	8675700
MGI:3800808	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(MtTPRMET)773Lng/0	FVB/N-Tg(MtTPRMET)773Lng	N	8675700
MGI:3801009	F	MP:0010249	lactation failure	Tnfsf11<tm1Pngr>/Tnfsf11<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6	N	11051546
MGI:3801009	F	MP:0006269	abnormal mammary gland growth during pregnancy	Tnfsf11<tm1Pngr>/Tnfsf11<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6	N	11051546
MGI:3801010	M	MP:0004852	decreased testis weight	Tg(Prnp-Abca1)EHol/0	involves: C57BL/6 * CBA	N	18202749
MGI:3801010	M	MP:0001156	abnormal spermatogenesis	Tg(Prnp-Abca1)EHol/0	involves: C57BL/6 * CBA	N	18202749
MGI:3801010	M	MP:0001154	seminiferous tubule degeneration	Tg(Prnp-Abca1)EHol/0	involves: C57BL/6 * CBA	N	18202749
MGI:3801010	M	MP:0003205	testicular atrophy	Tg(Prnp-Abca1)EHol/0	involves: C57BL/6 * CBA	N	18202749
MGI:3801010	M	MP:0020550	multinucleated giant male germ cells	Tg(Prnp-Abca1)EHol/0	involves: C57BL/6 * CBA	N	18202749
MGI:3801010	M	MP:0003830	abnormal testis development	Tg(Prnp-Abca1)EHol/0	involves: C57BL/6 * CBA	N	18202749
MGI:3801010	M	MP:0001925	male infertility	Tg(Prnp-Abca1)EHol/0	involves: C57BL/6 * CBA	N	18202749
MGI:3801010	M	MP:0001146	abnormal testis morphology	Tg(Prnp-Abca1)EHol/0	involves: C57BL/6 * CBA	N	18202749
MGI:3801016	F	MP:0010249	lactation failure	Tnfrsf11a<tm1Wjb>/Tnfrsf11a<tm1Wjb>	involves: 129X1/SvJ * C57BL/6	N	11051546
MGI:3801016	F	MP:0006269	abnormal mammary gland growth during pregnancy	Tnfrsf11a<tm1Wjb>/Tnfrsf11a<tm1Wjb>	involves: 129X1/SvJ * C57BL/6	N	11051546
MGI:3801100	M	MP:0001360	abnormal social investigation	Oxtr<tm1.2Wsy>/Oxtr<tm1.2Wsy>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL	N	18356275
MGI:3801100	F	MP:0003838	abnormal milk ejection	Oxtr<tm1.2Wsy>/Oxtr<tm1.2Wsy>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL	N	18356275
MGI:3801152	M	MP:0001354	increased aggression towards male mice	Tph2<tm1Mca>/Tph2<tm1Mca>	involves: 129S6/SvEvTac * C57BL/6J	N	18212115
MGI:3801152	M	MP:0003064	decreased coping response	Tph2<tm1Mca>/Tph2<tm1Mca>	involves: 129S6/SvEvTac * C57BL/6J	N	23467366
MGI:3801152	M	MP:0002272	abnormal nervous system electrophysiology	Tph2<tm1Mca>/Tph2<tm1Mca>	involves: 129S6/SvEvTac * C57BL/6J	N	23467366
MGI:3801168	M	MP:0006262	increased testis tumor incidence	Fzr1<tm1.1Mama>/Fzr1<+>	involves: BALB/cJ * C57BL/6 * SJL	N	18552834
MGI:3801298	M	MP:0001932	abnormal spermiogenesis	Ip6k1<tm1.1Snyd>/Ip6k1<tm1.1Snyd>	involves: 129X1/SvJ * BALB/c * C57BL/6	N	18268345
MGI:3801298	M	MP:0006380	abnormal spermatid morphology	Ip6k1<tm1.1Snyd>/Ip6k1<tm1.1Snyd>	involves: 129X1/SvJ * BALB/c * C57BL/6	N	18268345
MGI:3801298	M	MP:0001925	male infertility	Ip6k1<tm1.1Snyd>/Ip6k1<tm1.1Snyd>	involves: 129X1/SvJ * BALB/c * C57BL/6	N	18268345
MGI:3801298	M	MP:0005159	azoospermia	Ip6k1<tm1.1Snyd>/Ip6k1<tm1.1Snyd>	involves: 129X1/SvJ * BALB/c * C57BL/6	N	18268345
MGI:3801316	M	MP:0001922	reduced male fertility	Wwox<Gt(XG218)Byg>/Wwox<Gt(XG218)Byg>	involves: 129P2/OlaHsd	N	17823927
MGI:3801316	M	MP:0003205	testicular atrophy	Wwox<Gt(XG218)Byg>/Wwox<Gt(XG218)Byg>	involves: 129P2/OlaHsd	N	17823927
MGI:3801316	M	MP:0001152	increased Leydig cell number	Wwox<Gt(XG218)Byg>/Wwox<Gt(XG218)Byg>	involves: 129P2/OlaHsd	N	17823927
MGI:3801316	M	MP:0001154	seminiferous tubule degeneration	Wwox<Gt(XG218)Byg>/Wwox<Gt(XG218)Byg>	involves: 129P2/OlaHsd	N	17823927
MGI:3801325	M	MP:0001925	male infertility	Sptbn4<qv-11J>/Sptbn4<qv-11J>	C57BL/6J-Sptbn4<qv-11J>/J	N	MGI:3799697
MGI:3801485	M	MP:0000120	malocclusion	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C3H/HeSn	N	16467389
MGI:3801485	M	MP:0001263	weight loss	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C3H/HeSn	N	16467389
MGI:3801485	M	MP:0001732	postnatal growth retardation	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C3H/HeSn	N	16467389
MGI:3801485	M	MP:0005202	lethargy	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C3H/HeSn	N	16467389
MGI:3801485	M	MP:0002083	premature death	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C3H/HeSn	N	16467389
MGI:3801486	M	MP:0002083	premature death	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ	N	16467389
MGI:3801487	M	MP:0001406	abnormal gait	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0001513	limb grasping	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0002062	abnormal associative learning	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0002065	abnormal fear/anxiety-related behavior	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0001402	decreased locomotor activity	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0001405	impaired coordination	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0001405	impaired coordination	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18557922
MGI:3801487	M	MP:0002083	premature death	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0002757	decreased vertical activity	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18557922
MGI:3801487	M	MP:0001469	abnormal contextual conditioning behavior	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0001263	weight loss	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0001454	abnormal cued conditioning behavior	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0001511	disheveled coat	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0005386	behavior/neurological phenotype	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	18557922
MGI:3801487	M	MP:0000951	sporadic seizures	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0000745	tremors	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0001364	decreased anxiety-related response	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0001392	abnormal locomotor behavior	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0001954	respiratory distress	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0001732	postnatal growth retardation	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0002066	abnormal motor capabilities/coordination/movement	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0002175	decreased brain weight	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801487	M	MP:0002098	abnormal vibrissa morphology	Mecp2<tm1Pplt>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	16467389
MGI:3801488	F	MP:0002757	decreased vertical activity	Mecp2<tm1Pplt>/Mecp2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18557922
MGI:3801488	F	MP:0001405	impaired coordination	Mecp2<tm1Pplt>/Mecp2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18557922
MGI:3802653	M	MP:0001922	reduced male fertility	Del(2Hoxd11-Hoxd13)29Ddu/+,Hoxd13<spdh>/Hoxd13<+>	involves: 129S2/SvPas * C3HeB/FeJLe * C57BL/6J	N	11543619
MGI:3802654	M	MP:0001922	reduced male fertility	Hoxd13<spdh>/Hoxd13<tm1Ddu>	involves: 129S2/SvPas * C3HeB/FeJLe * C57BL/6J	N	11543619
MGI:3802703	M	MP:0002566	abnormal sexual interaction	Gusb<mps-3J>/Gusb<mps-3J>	C57BL/6J-Gusb<mps-3J>/J	N	MGI:3801433
MGI:3802771	F	MP:0008688	decreased interleukin-2 secretion	Arhgef6<tm1Kdf>/Arhgef6<tm1Kdf>	involves: 129P2/OlaHsd * C57BL/6	N	18378701
MGI:3802771	F	MP:0002444	abnormal T cell physiology	Arhgef6<tm1Kdf>/Arhgef6<tm1Kdf>	involves: 129P2/OlaHsd * C57BL/6	N	18378701
MGI:3802771	F	MP:0005095	decreased T cell proliferation	Arhgef6<tm1Kdf>/Arhgef6<tm1Kdf>	involves: 129P2/OlaHsd * C57BL/6	N	18378701
MGI:3802771	F	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Arhgef6<tm1Kdf>/Arhgef6<tm1Kdf>	involves: 129P2/OlaHsd * C57BL/6	N	18378701
MGI:3802771	F	MP:0005016	decreased lymphocyte cell number	Arhgef6<tm1Kdf>/Arhgef6<tm1Kdf>	involves: 129P2/OlaHsd * C57BL/6	N	18378701
MGI:3802771	F	MP:0001800	abnormal humoral immune response	Arhgef6<tm1Kdf>/Arhgef6<tm1Kdf>	involves: 129P2/OlaHsd * C57BL/6	N	18378701
MGI:3802771	F	MP:0002458	abnormal B cell number	Arhgef6<tm1Kdf>/Arhgef6<tm1Kdf>	involves: 129P2/OlaHsd * C57BL/6	N	18378701
MGI:3802771	F	MP:0014471	enhanced B cell migration	Arhgef6<tm1Kdf>/Arhgef6<tm1Kdf>	involves: 129P2/OlaHsd * C57BL/6	N	18378701
MGI:3802771	F	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Arhgef6<tm1Kdf>/Arhgef6<tm1Kdf>	involves: 129P2/OlaHsd * C57BL/6	N	18378701
MGI:3802771	F	MP:0008211	decreased mature B cell number	Arhgef6<tm1Kdf>/Arhgef6<tm1Kdf>	involves: 129P2/OlaHsd * C57BL/6	N	18378701
MGI:3802771	F	MP:0005093	decreased B cell proliferation	Arhgef6<tm1Kdf>/Arhgef6<tm1Kdf>	involves: 129P2/OlaHsd * C57BL/6	N	18378701
MGI:3802836	F	MP:0011125	decreased primary ovarian follicle number	Prop1<df>/Prop1<df>	DF	N	31987917
MGI:3802836	F	MP:0031381	decreased secondary ovarian follicle number	Prop1<df>/Prop1<df>	DF	N	31987917
MGI:3802836	F	MP:0001131	abnormal ovarian follicle morphology	Prop1<df>/Prop1<df>	DF	N	31987917
MGI:3802836	F	MP:0011120	increased primordial ovarian follicle number	Prop1<df>/Prop1<df>	DF	N	31987917
MGI:3802836	F	MP:0008868	abnormal granulosa cell morphology	Prop1<df>/Prop1<df>	DF	N	31987917
MGI:3802836	F	MP:0011129	decreased tertiary ovarian follicle number	Prop1<df>/Prop1<df>	DF	N	31987917
MGI:3803013	F	MP:0001926	female infertility	Mta2<tm1.1Yzha>/Mta2<tm1.1Yzha>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	18353770
MGI:3803199	F	MP:0003632	abnormal nervous system morphology	Aire<tm1Mand>/Aire<+>	NOD.129P2-Aire<tm1Mand>	N	22490868
MGI:3803199	F	MP:0000753	paralysis	Aire<tm1Mand>/Aire<+>	NOD.129P2-Aire<tm1Mand>	N	22490868
MGI:3803593	F	MP:0014272	increased ovary secretion	Chst8<tm1.1Jub>/Chst8<tm1.1Jub>	B6.129X1-Chst8<tm1.1Jub>	N	18431515
MGI:3803593	F	MP:0009006	prolonged estrous cycle	Chst8<tm1.1Jub>/Chst8<tm1.1Jub>	B6.129X1-Chst8<tm1.1Jub>	N	18431515
MGI:3803593	F	MP:0001120	abnormal uterus morphology	Chst8<tm1.1Jub>/Chst8<tm1.1Jub>	B6.129X1-Chst8<tm1.1Jub>	N	18431515
MGI:3803593	F	MP:0002681	increased corpora lutea number	Chst8<tm1.1Jub>/Chst8<tm1.1Jub>	B6.129X1-Chst8<tm1.1Jub>	N	18431515
MGI:3803593	F	MP:0001385	pup cannibalization	Chst8<tm1.1Jub>/Chst8<tm1.1Jub>	B6.129X1-Chst8<tm1.1Jub>	N	18431515
MGI:3803593	M	MP:0004928	increased epididymis weight	Chst8<tm1.1Jub>/Chst8<tm1.1Jub>	B6.129X1-Chst8<tm1.1Jub>	N	18431515
MGI:3803593	F	MP:0001128	ovary hyperplasia	Chst8<tm1.1Jub>/Chst8<tm1.1Jub>	B6.129X1-Chst8<tm1.1Jub>	N	18431515
MGI:3803593	F	MP:0004904	increased uterus weight	Chst8<tm1.1Jub>/Chst8<tm1.1Jub>	B6.129X1-Chst8<tm1.1Jub>	N	18431515
MGI:3803593	M	MP:0004851	increased testis weight	Chst8<tm1.1Jub>/Chst8<tm1.1Jub>	B6.129X1-Chst8<tm1.1Jub>	N	18431515
MGI:3803593	M	MP:0004909	increased seminal vesicle weight	Chst8<tm1.1Jub>/Chst8<tm1.1Jub>	B6.129X1-Chst8<tm1.1Jub>	N	18431515
MGI:3803668	M	MP:0001148	enlarged testis	Lasp1<tm1Chew>/Lasp1<tm1Chew>	involves: 129X1/SvJ * C57BL/6J	N	18483181
MGI:3803668	M	MP:0001157	small seminal vesicle	Lasp1<tm1Chew>/Lasp1<tm1Chew>	involves: 129X1/SvJ * C57BL/6J	N	18483181
MGI:3803670	F	MP:0003578	absent ovary	Wt1<tm1Mlh>/Wt1<tm1Mlh>	involves: 129P2/OlaHsd * C57BL/6	N	18040647
MGI:3803670	M	MP:0006415	absent testes	Wt1<tm1Mlh>/Wt1<tm1Mlh>	involves: 129P2/OlaHsd * C57BL/6	N	18040647
MGI:3803729	M	MP:0001925	male infertility	Tshr<hyt>/Tshr<hyt>	involves: BALB/cByJ * RF/J	N	7209519
MGI:3803729	F	MP:0001926	female infertility	Tshr<hyt>/Tshr<hyt>	involves: BALB/cByJ * RF/J	N	7209519
MGI:3804205	M	MP:0002753	dilated heart left ventricle	Ace2<tm1Hira>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	16505206
MGI:3804205	M	MP:0005630	increased lung weight	Ace2<tm1Hira>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	16505206
MGI:3804205	M	MP:0003141	cardiac fibrosis	Ace2<tm1Hira>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	16505206
MGI:3804205	M	MP:0006138	congestive heart failure	Ace2<tm1Hira>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	16505206
MGI:3804205	M	MP:0010018	pulmonary vascular congestion	Ace2<tm1Hira>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	16505206
MGI:3804205	M	MP:0005598	decreased heart ventricle muscle contractility	Ace2<tm1Hira>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	16505206
MGI:3804205	M	MP:0009763	increased susceptibility to induced morbidity/mortality	Ace2<tm1Hira>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	16505206
MGI:3804205	M	MP:0005608	cardiac interstitial fibrosis	Ace2<tm1Hira>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	16505206
MGI:3804205	M	MP:0002833	increased heart weight	Ace2<tm1Hira>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	16505206
MGI:3804205	M	MP:0031232	increased circulating angiotensin II level	Ace2<tm1Hira>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	16505206
MGI:3804256	F	MP:0004855	increased ovary weight	Ddx20<tm1Yosa>/Ddx20<+>	involves: 129/Sv * C57BL/6	N	18258677
MGI:3804256	F	MP:0001131	abnormal ovarian follicle morphology	Ddx20<tm1Yosa>/Ddx20<+>	involves: 129/Sv * C57BL/6	N	18258677
MGI:3804256	F	MP:0001927	abnormal estrous cycle	Ddx20<tm1Yosa>/Ddx20<+>	involves: 129/Sv * C57BL/6	N	18258677
MGI:3804256	F	MP:0009017	prolonged estrus	Ddx20<tm1Yosa>/Ddx20<+>	involves: 129/Sv * C57BL/6	N	18258677
MGI:3804262	M	MP:0001925	male infertility	Del(16Tssk1-Tssk2)1Joch/+	chimera involves: 129X1/SvJ	N	18533145
MGI:3804262	M	MP:0002216	abnormal seminiferous tubule morphology	Del(16Tssk1-Tssk2)1Joch/+	chimera involves: 129X1/SvJ	N	18533145
MGI:3804262	M	MP:0001155	arrest of spermatogenesis	Del(16Tssk1-Tssk2)1Joch/+	chimera involves: 129X1/SvJ	N	18533145
MGI:3804262	M	MP:0005159	azoospermia	Del(16Tssk1-Tssk2)1Joch/+	chimera involves: 129X1/SvJ	N	18533145
MGI:3804262	M	MP:0001156	abnormal spermatogenesis	Del(16Tssk1-Tssk2)1Joch/+	chimera involves: 129X1/SvJ	N	18533145
MGI:3804262	M	MP:0001147	small testis	Del(16Tssk1-Tssk2)1Joch/+	chimera involves: 129X1/SvJ	N	18533145
MGI:3804262	M	MP:0004852	decreased testis weight	Del(16Tssk1-Tssk2)1Joch/+	chimera involves: 129X1/SvJ	N	18533145
MGI:3804262	M	MP:0006380	abnormal spermatid morphology	Del(16Tssk1-Tssk2)1Joch/+	chimera involves: 129X1/SvJ	N	18533145
MGI:3804422	M	MP:0001147	small testis	Pdpk1<tm1Dral>/Pdpk1<tm1Dral>	B6.129P2-Pdpk1<tm1Dral>	N	18347057
MGI:3804459	M	MP:0006380	abnormal spermatid morphology	Sox8<tm1Mkob>/Sox8<tm1Mkob>	involves: 129S7/SvEvBrd	N	18342849
MGI:3804459	M	MP:0002631	abnormal epididymis morphology	Sox8<tm1Mkob>/Sox8<tm1Mkob>	involves: 129S7/SvEvBrd	N	18342849
MGI:3804459	M	MP:0004852	decreased testis weight	Sox8<tm1Mkob>/Sox8<tm1Mkob>	involves: 129S7/SvEvBrd	N	18342849
MGI:3804459	M	MP:0002673	abnormal sperm number	Sox8<tm1Mkob>/Sox8<tm1Mkob>	involves: 129S7/SvEvBrd	N	18342849
MGI:3804459	M	MP:0004182	abnormal spermiation	Sox8<tm1Mkob>/Sox8<tm1Mkob>	involves: 129S7/SvEvBrd	N	18342849
MGI:3804459	M	MP:0031389	abnormal ectoplasmic specialization morphology	Sox8<tm1Mkob>/Sox8<tm1Mkob>	involves: 129S7/SvEvBrd	N	18342849
MGI:3804459	M	MP:0002784	abnormal Sertoli cell morphology	Sox8<tm1Mkob>/Sox8<tm1Mkob>	involves: 129S7/SvEvBrd	N	18342849
MGI:3804459	M	MP:0001925	male infertility	Sox8<tm1Mkob>/Sox8<tm1Mkob>	involves: 129S7/SvEvBrd	N	18342849
MGI:3804459	M	MP:0001156	abnormal spermatogenesis	Sox8<tm1Mkob>/Sox8<tm1Mkob>	involves: 129S7/SvEvBrd	N	18342849
MGI:3804459	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Sox8<tm1Mkob>/Sox8<tm1Mkob>	involves: 129S7/SvEvBrd	N	18342849
MGI:3804459	M	MP:0002675	asthenozoospermia	Sox8<tm1Mkob>/Sox8<tm1Mkob>	involves: 129S7/SvEvBrd	N	18342849
MGI:3804459	M	MP:0001145	abnormal male reproductive system morphology	Sox8<tm1Mkob>/Sox8<tm1Mkob>	involves: 129S7/SvEvBrd	N	18342849
MGI:3804459	M	MP:0001922	reduced male fertility	Sox8<tm1Mkob>/Sox8<tm1Mkob>	involves: 129S7/SvEvBrd	N	18342849
MGI:3804535	F	MP:0001728	failure of embryo implantation	Kif11<tm1Much>/Kif11<tm1Much>	involves: 129S2/SvPas * C57BL/6	N	18474226
MGI:3804646	F	MP:0000372	irregular coat pigmentation	Atp7a<Mo-pew>/Atp7a<+>	CBA/J-Atp7a<Mo-pew>	N	MGI:71784
MGI:3804646	F	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-pew>/Atp7a<+>	CBA/J-Atp7a<Mo-pew>	N	MGI:71784
MGI:3804646	F	MP:0000421	mottled coat	Atp7a<Mo-pew>/Atp7a<+>	CBA/J-Atp7a<Mo-pew>	N	MGI:71784
MGI:3804647	M	MP:0010768	mortality/aging	Atp7a<Mo-pew>/Y	CBA/J-Atp7a<Mo-pew>	Y	MGI:71784
MGI:3804647	M	MP:0000371	diluted coat color	Atp7a<Mo-pew>/Y	CBA/J-Atp7a<Mo-pew>	N	MGI:71784
MGI:3804647	M	MP:0005389	reproductive system phenotype	Atp7a<Mo-pew>/Y	CBA/J-Atp7a<Mo-pew>	Y	MGI:71784
MGI:3804647	M	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-pew>/Y	CBA/J-Atp7a<Mo-pew>	N	MGI:86479
MGI:3804647	M	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-pew>/Y	CBA/J-Atp7a<Mo-pew>	N	MGI:71784
MGI:3804683	M	MP:0002743	glomerulonephritis	Nba10<NZB>/Nba10<NZB>,Tlr7<tm1Aki>/Y,X/Yaa	B6.Cg-Nba10<NZB> Tlr7<tm1Aki> Yaa	N	18606711
MGI:3804683	M	MP:0002723	abnormal immune serum protein physiology	Nba10<NZB>/Nba10<NZB>,Tlr7<tm1Aki>/Y,X/Yaa	B6.Cg-Nba10<NZB> Tlr7<tm1Aki> Yaa	N	18606711
MGI:3804683	M	MP:0000220	increased monocyte cell number	Nba10<NZB>/Nba10<NZB>,Tlr7<tm1Aki>/Y,X/Yaa	B6.Cg-Nba10<NZB> Tlr7<tm1Aki> Yaa	N	18606711
MGI:3804683	M	MP:0004829	increased anti-chromatin antibody level	Nba10<NZB>/Nba10<NZB>,Tlr7<tm1Aki>/Y,X/Yaa	B6.Cg-Nba10<NZB> Tlr7<tm1Aki> Yaa	N	18606711
MGI:3804851	M	MP:0005159	azoospermia	Tg(Prnp-ATXN3)BVcg/Tg(Prnp-ATXN3)BVcg	involves: C3H/HeJ * C57BL/6	N	16282980
MGI:3804851	M	MP:0014052	increased male germ cell apoptosis	Tg(Prnp-ATXN3)BVcg/Tg(Prnp-ATXN3)BVcg	involves: C3H/HeJ * C57BL/6	N	16282980
MGI:3804851	M	MP:0003205	testicular atrophy	Tg(Prnp-ATXN3)BVcg/Tg(Prnp-ATXN3)BVcg	involves: C3H/HeJ * C57BL/6	N	16282980
MGI:3804853	M	MP:0005169	abnormal male meiosis	In(5)30Rk/+	involves: M. m. domesticus poschiavinus	N	MGI:71289
MGI:3804854	M	MP:0001922	reduced male fertility	Tg(Prnp-ATXN3)CVcg/0	involves: C3H/HeJ * C57BL/6	N	16282980
MGI:3804855	M	MP:0001146	abnormal testis morphology	Tg(Prnp-ATXN3)CVcg/Tg(Prnp-ATXN3)CVcg	involves: C3H/HeJ * C57BL/6	N	16282980
MGI:3804855	M	MP:0001922	reduced male fertility	Tg(Prnp-ATXN3)CVcg/Tg(Prnp-ATXN3)CVcg	involves: C3H/HeJ * C57BL/6	N	16282980
MGI:3804856	M	MP:0005169	abnormal male meiosis	In(15)35Rk/+	involves: C57BL/6J * DBA/2J	N	MGI:71289
MGI:3804867	M	MP:0000659	prostate gland hyperplasia	Wdr77<tm1Zwan>/Wdr77<+>	involves: 129P2/OlaHsd * C57BL/6J	N	17032745
MGI:3804867	M	MP:0001167	prostate gland epithelial hyperplasia	Wdr77<tm1Zwan>/Wdr77<+>	involves: 129P2/OlaHsd * C57BL/6J	N	17032745
MGI:3804867	M	MP:0001168	abnormal prostate gland epithelium morphology	Wdr77<tm1Zwan>/Wdr77<+>	involves: 129P2/OlaHsd * C57BL/6J	N	17032745
MGI:3805109	M	MP:0002566	abnormal sexual interaction	Gria1<tm1Rsp>/Gria1<tm1Rsp>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15344919
MGI:3805109	M	MP:0001360	abnormal social investigation	Gria1<tm1Rsp>/Gria1<tm1Rsp>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15344919
MGI:3805196	F	MP:0005385	cardiovascular system phenotype	Vegfd<tm1Mach>/Vegfd<tm1Mach>,Vegfc<tm1Ali>/Vegfc<tm1Ali>	involves: 129S1/Sv * 129X1/SvJ	Y	18519586
MGI:3805196	F	MP:0002080	prenatal lethality	Vegfd<tm1Mach>/Vegfd<tm1Mach>,Vegfc<tm1Ali>/Vegfc<tm1Ali>	involves: 129S1/Sv * 129X1/SvJ	N	18519586
MGI:3805196	F	MP:0008778	abnormal lymphangiogenesis	Vegfd<tm1Mach>/Vegfd<tm1Mach>,Vegfc<tm1Ali>/Vegfc<tm1Ali>	involves: 129S1/Sv * 129X1/SvJ	N	18519586
MGI:3805196	F	MP:0001879	abnormal lymphatic vessel morphology	Vegfd<tm1Mach>/Vegfd<tm1Mach>,Vegfc<tm1Ali>/Vegfc<tm1Ali>	involves: 129S1/Sv * 129X1/SvJ	N	18519586
MGI:3805200	F	MP:0000628	abnormal mammary gland development	Hras<tm2Xbr>/Hras<tm2Xbr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18483625
MGI:3805200	F	MP:0000630	mammary gland hyperplasia	Hras<tm2Xbr>/Hras<tm2Xbr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18483625
MGI:3805200	F	MP:0000662	abnormal branching of the mammary ductal tree	Hras<tm2Xbr>/Hras<tm2Xbr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18483625
MGI:3805208	F	MP:0001729	impaired embryo implantation	Rybp<tm1Nisa>/Rybp<tm1Nisa>	involves: 129S1/Sv * 129X1/SvJ * ICR	N	16055728
MGI:3805380	M	MP:0005385	cardiovascular system phenotype	Fgf16<tm1Paca>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	Y	18565327
MGI:3805380	M	MP:0003140	dilated heart atrium	Fgf16<tm1Paca>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	18565327
MGI:3805380	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Fgf16<tm1Paca>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	18565327
MGI:3805380	M	MP:0003984	embryonic growth retardation	Fgf16<tm1Paca>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	18565327
MGI:3805380	M	MP:0006337	abnormal first pharyngeal arch morphology	Fgf16<tm1Paca>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	18565327
MGI:3805380	M	MP:0001634	internal hemorrhage	Fgf16<tm1Paca>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	18565327
MGI:3805380	M	MP:0005294	abnormal heart ventricle morphology	Fgf16<tm1Paca>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	18565327
MGI:3805380	M	MP:0008022	dilated heart ventricle	Fgf16<tm1Paca>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	18565327
MGI:3805380	M	MP:0000280	thin ventricular wall	Fgf16<tm1Paca>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	18565327
MGI:3805380	M	MP:0000295	trabecula carnea hypoplasia	Fgf16<tm1Paca>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	18565327
MGI:3805380	M	MP:0000266	abnormal heart morphology	Fgf16<tm1Paca>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	18565327
MGI:3805686	M	MP:0001925	male infertility	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	N	14794889
MGI:3805686	F	MP:0001927	abnormal estrous cycle	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	N	14794889
MGI:3805686	M	MP:0002286	cryptorchism	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	N	14794889
MGI:3805686	F	MP:0002637	small uterus	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	N	14794889
MGI:3805686	M	MP:0002566	abnormal sexual interaction	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	N	14794889
MGI:3805686	M	MP:0003415	priapism	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	N	14794889
MGI:3805686	M	MP:0001147	small testis	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	N	14794889
MGI:3805686	F	MP:0001127	small ovary	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	N	14794889
MGI:3805686	F	MP:0001926	female infertility	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	N	14794889
MGI:3805864	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pik3ca<tm1Jjz>/Pik3ca<tm1Jjz>,Tg(Pbsn-cre)4Prb/0	involves: 129 * C57BL/6 * DBA/2	N	18594509
MGI:3805865	F	MP:0001926	female infertility	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129 * 129S4/SvJae * C57BL/6 * DBA/2	N	19033462
MGI:3805865	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129 * 129S4/SvJae * C57BL/6 * DBA/2	N	19033462
MGI:3805865	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129 * 129S4/SvJae * C57BL/6 * DBA/2	N	19033462
MGI:3805865	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129 * 129S4/SvJae * C57BL/6 * DBA/2	N	18594509
MGI:3805890	M	MP:0003631	nervous system phenotype	L1cam<tm1Mtei>/Y	involves: 129	Y	18447583
MGI:3805979	F	MP:0001926	female infertility	Prdm14<tm1Sait>/Prdm14<tm1Sait>	B6.129P2-Prdm14<tm1Sait>	N	18622394
MGI:3805979	M	MP:0001925	male infertility	Prdm14<tm1Sait>/Prdm14<tm1Sait>	B6.129P2-Prdm14<tm1Sait>	N	18622394
MGI:3806011	F	MP:0010389	mosaic coat color	Atp7a<Mo-2Btlr>/Atp7a<+>	C57BL/6J-Atp7a<Mo-2Btlr>	N	22869751
MGI:3806011	F	MP:0010389	mosaic coat color	Atp7a<Mo-2Btlr>/Atp7a<+>	C57BL/6J-Atp7a<Mo-2Btlr>	N	MGI:3805886
MGI:3806012	M	MP:0011085	postnatal lethality, complete penetrance	Atp7a<Mo-2Btlr>/Y	C57BL/6J-Atp7a<Mo-2Btlr>	N	22869751
MGI:3806012	M	MP:0005171	absent coat pigmentation	Atp7a<Mo-2Btlr>/Y	C57BL/6J-Atp7a<Mo-2Btlr>	N	22869751
MGI:3806012	M	MP:0001186	pigmentation phenotype	Atp7a<Mo-2Btlr>/Y	C57BL/6J-Atp7a<Mo-2Btlr>	Y	MGI:3805886
MGI:3806012	M	MP:0005171	absent coat pigmentation	Atp7a<Mo-2Btlr>/Y	C57BL/6J-Atp7a<Mo-2Btlr>	N	MGI:3805886
MGI:3806012	M	MP:0011101	prenatal lethality, incomplete penetrance	Atp7a<Mo-2Btlr>/Y	C57BL/6J-Atp7a<Mo-2Btlr>	N	MGI:3805886
MGI:3806012	M	MP:0011085	postnatal lethality, complete penetrance	Atp7a<Mo-2Btlr>/Y	C57BL/6J-Atp7a<Mo-2Btlr>	N	MGI:3805886
MGI:3806012	M	MP:0011101	prenatal lethality, incomplete penetrance	Atp7a<Mo-2Btlr>/Y	C57BL/6J-Atp7a<Mo-2Btlr>	N	22869751
MGI:3806014	F	MP:0001125	abnormal oocyte morphology	Padi6<tm1.1Jgo>/Padi6<tm1.1Jgo>	involves: BALB/cJ	N	17587491
MGI:3806014	F	MP:0001926	female infertility	Padi6<tm1.1Jgo>/Padi6<tm1.1Jgo>	involves: BALB/cJ	N	17587491
MGI:3806019	F	MP:0001125	abnormal oocyte morphology	Padi6<tm1.1Jgo>/Padi6<tm1.1Jgo>	Not Specified	N	18599511
MGI:3806025	F	MP:0011086	postnatal lethality, incomplete penetrance	L1cam<tm1Sor>/L1cam<+>,Nrcam<tm1Gmt>/Nrcam<tm1Gmt>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster	N	11564762
MGI:3806030	M	MP:0011086	postnatal lethality, incomplete penetrance	L1cam<tm1Sor>/Y,Nrcam<tm1Gmt>/Nrcam<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster	N	11564762
MGI:3806032	M	MP:0000886	abnormal cerebellar granule layer morphology	L1cam<tm1Sor>/Y,Nrcam<tm1Gmt>/Nrcam<tm1Gmt>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster	N	11564762
MGI:3806032	M	MP:0000852	small cerebellum	L1cam<tm1Sor>/Y,Nrcam<tm1Gmt>/Nrcam<tm1Gmt>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster	N	11564762
MGI:3806032	M	MP:0004097	abnormal cerebellar cortex morphology	L1cam<tm1Sor>/Y,Nrcam<tm1Gmt>/Nrcam<tm1Gmt>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster	N	11564762
MGI:3806032	M	MP:0002082	postnatal lethality	L1cam<tm1Sor>/Y,Nrcam<tm1Gmt>/Nrcam<tm1Gmt>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster	N	11564762
MGI:3806032	M	MP:0000857	abnormal cerebellar foliation	L1cam<tm1Sor>/Y,Nrcam<tm1Gmt>/Nrcam<tm1Gmt>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster	N	11564762
MGI:3806032	M	MP:0001262	decreased body weight	L1cam<tm1Sor>/Y,Nrcam<tm1Gmt>/Nrcam<tm1Gmt>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster	N	11564762
MGI:3806032	M	MP:0000854	abnormal cerebellum development	L1cam<tm1Sor>/Y,Nrcam<tm1Gmt>/Nrcam<tm1Gmt>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster	N	11564762
MGI:3806032	M	MP:0000872	abnormal cerebellum external granule cell layer morphology	L1cam<tm1Sor>/Y,Nrcam<tm1Gmt>/Nrcam<tm1Gmt>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster	N	11564762
MGI:3806097	F	MP:0009763	increased susceptibility to induced morbidity/mortality	Vsig4<tm1Gne>/Vsig4<tm1Gne>	involves: C57BL/6N	N	16530040
MGI:3806097	F	MP:0002412	increased susceptibility to bacterial infection	Vsig4<tm1Gne>/Vsig4<tm1Gne>	involves: C57BL/6N	N	16530040
MGI:3806098	F	MP:0005387	immune system phenotype	C3<tm1Hrc>/C3<tm1Hrc>,Vsig4<tm1Gne>/Vsig4<tm1Gne>	involves: 129/Sv * C57BL/6N	Y	16530040
MGI:3806101	F	MP:0005464	abnormal platelet physiology	C3<tm1Hrc>/C3<tm1Hrc>,Cd55<tm1Song>/Cd55<tm1Song>,Cr1l<tm1Hmo>/Cr1l<tm1Hmo>,Vsig4<tm1Gne>/Vsig4<tm1Gne>	involves: 129/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6N	N	18524992
MGI:3806241	F	MP:0011091	prenatal lethality, complete penetrance	Fgf16<tm1Paca>/Fgf16<tm1Paca>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	18565327
MGI:3806253	M	MP:0000702	enlarged lymph nodes	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806253	M	MP:0001861	lung inflammation	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806253	M	MP:0000218	increased leukocyte cell number	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806253	M	MP:0001828	abnormal T cell activation	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806253	M	MP:0002083	premature death	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806253	M	MP:0001860	liver inflammation	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806253	M	MP:0001863	blood vessel inflammation	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806253	M	MP:0008559	abnormal interferon-gamma secretion	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806253	M	MP:0008698	abnormal interleukin-4 secretion	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806253	M	MP:0000691	enlarged spleen	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806253	M	MP:0008078	increased CD8-positive, alpha-beta T cell number	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806254	F	MP:0000702	enlarged lymph nodes	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806254	F	MP:0008698	abnormal interleukin-4 secretion	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806254	F	MP:0001863	blood vessel inflammation	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806254	F	MP:0004941	abnormal regulatory T cell morphology	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806254	F	MP:0000218	increased leukocyte cell number	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806254	F	MP:0002083	premature death	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806254	F	MP:0001828	abnormal T cell activation	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806254	F	MP:0000691	enlarged spleen	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806254	F	MP:0008078	increased CD8-positive, alpha-beta T cell number	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806254	F	MP:0008559	abnormal interferon-gamma secretion	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806254	F	MP:0001861	lung inflammation	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806254	F	MP:0001860	liver inflammation	Drosha<tm1Litt>/Drosha<tm1.1Litt>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	18725527
MGI:3806255	M	MP:0000702	enlarged lymph nodes	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	18725527
MGI:3806255	M	MP:0001860	liver inflammation	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	18725527
MGI:3806255	M	MP:0001861	lung inflammation	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	18725527
MGI:3806255	M	MP:0000691	enlarged spleen	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	18725527
MGI:3806255	M	MP:0001863	blood vessel inflammation	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	18725527
MGI:3806255	M	MP:0002083	premature death	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ	N	18725527
MGI:3806256	F	MP:0002083	premature death	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ	N	18725527
MGI:3806256	F	MP:0001860	liver inflammation	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ	N	18725527
MGI:3806256	F	MP:0001861	lung inflammation	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ	N	18725527
MGI:3806256	F	MP:0000702	enlarged lymph nodes	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ	N	18725527
MGI:3806256	F	MP:0000691	enlarged spleen	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ	N	18725527
MGI:3806256	F	MP:0001863	blood vessel inflammation	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<tm4(YFP/icre)Ayr>	involves: 129S1/Sv * 129X1/SvJ	N	18725527
MGI:3806609	F	MP:0014126	increased mammary gland apoptosis	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129S4/SvJae	N	18559482
MGI:3806609	F	MP:0006271	abnormal involution of the mammary gland	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129S4/SvJae	N	18559482
MGI:3806609	F	MP:0010173	increased mammary gland epithelial cell proliferation	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129S4/SvJae	N	18559482
MGI:3806610	F	MP:0014126	increased mammary gland apoptosis	Ccne1<tm1Jro>/Ccne1<tm1Jro>	involves: 129/Sv * 129S4/SvJaeSor	N	18559482
MGI:3806610	F	MP:0010173	increased mammary gland epithelial cell proliferation	Ccne1<tm1Jro>/Ccne1<tm1Jro>	involves: 129/Sv * 129S4/SvJaeSor	N	18559482
MGI:3806703	M	MP:0002169	no abnormal phenotype detected	Arx<tm1Gldn>/Y	involves: 129/Sv * C57BL/6	N	18799476
MGI:3806704	F	MP:0002169	no abnormal phenotype detected	Arx<tm1Gldn>/Arx<tm1Gldn>	involves: 129/Sv * C57BL/6	N	18799476
MGI:3806705	M	MP:0000788	abnormal cerebral cortex morphology	Arx<tm1Gldn>/Y,Tg(Pou3f4-cre)32Cren/0	involves: 129/Sv * C57BL/6 * CD-1	N	18799476
MGI:3806705	M	MP:0000819	abnormal olfactory bulb morphology	Arx<tm1Gldn>/Y,Tg(Pou3f4-cre)32Cren/0	involves: 129/Sv * C57BL/6 * CD-1	N	18799476
MGI:3806705	M	MP:0000774	decreased brain size	Arx<tm1Gldn>/Y,Tg(Pou3f4-cre)32Cren/0	involves: 129/Sv * C57BL/6 * CD-1	N	18799476
MGI:3806844	F	MP:0002679	abnormal corpus luteum morphology	E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	N	18594513
MGI:3806844	F	MP:0005158	ovary hypoplasia	E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	N	18594513
MGI:3806844	F	MP:0001926	female infertility	E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	N	18594513
MGI:3806844	M	MP:0001925	male infertility	E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	N	18594513
MGI:3806844	M	MP:0001940	testis hypoplasia	E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	N	18594513
MGI:3806851	M	MP:0001146	abnormal testis morphology	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16406039
MGI:3806851	M	MP:0006417	rete testis obstruction	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16406039
MGI:3806851	M	MP:0006416	abnormal rete testis morphology	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16406039
MGI:3806851	M	MP:0009248	small caput epididymis	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16406039
MGI:3806851	M	MP:0001925	male infertility	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16406039
MGI:3806851	M	MP:0002631	abnormal epididymis morphology	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16406039
MGI:3806851	M	MP:0004884	abnormal testis physiology	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16406039
MGI:3806851	M	MP:0014193	decreased epididymal cell proliferation	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16406039
MGI:3806851	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16406039
MGI:3806851	M	MP:0004932	epididymis hypoplasia	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16406039
MGI:3806851	M	MP:0004933	abnormal epididymis epithelium morphology	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16406039
MGI:3806851	M	MP:0004728	abnormal efferent ductules of testis morphology	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16406039
MGI:3806851	M	MP:0003595	epididymal cyst	Lgr4<Gt(pGT0TMpfs)1Wcs>/Lgr4<Gt(pGT0TMpfs)1Wcs>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	16406039
MGI:3806977	F	MP:0000592	short tail	Phex<Pug>/Phex<+>	involves: C57BL/6J	N	17710565
MGI:3806977	F	MP:0014322	short hindlimb	Phex<Pug>/Phex<+>	involves: C57BL/6J	N	17710565
MGI:3806977	F	MP:0001265	decreased body size	Phex<Pug>/Phex<+>	involves: C57BL/6J	N	17710565
MGI:3806978	F	MP:0002427	disproportionate dwarf	Phex<Pug>/Phex<Pug>	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0006397	disorganized long bone epiphyseal plate	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0001258	decreased body length	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0002427	disproportionate dwarf	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0000063	decreased bone mineral density	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0000198	decreased circulating phosphate level	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0001265	decreased body size	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0002896	abnormal bone mineralization	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0005508	abnormal skeleton morphology	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0006281	abnormal tail development	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0014104	decreased chondrocyte apoptosis	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0010878	increased trabecular bone volume	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0000592	short tail	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0000195	decreased circulating calcium level	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3806979	M	MP:0014322	short hindlimb	Phex<Pug>/Y	involves: C57BL/6J	N	17710565
MGI:3807072	M	MP:0004229	abnormal embryonic erythropoiesis	Cdx4<tm1.1Gqda>/Y	involves: 129S4/SvJae * C57BL/6	N	18511567
MGI:3807073	F	MP:0004229	abnormal embryonic erythropoiesis	Cdx4<tm1.1Gqda>/Cdx4<tm1.1Gqda>	involves: 129S4/SvJae * C57BL/6	N	18511567
MGI:3807083	M	MP:0031138	testicular hemorrhage	Foxs1<tm1Kmor>/Foxs1<tm1Kmor>	involves: 129P2/OlaHsd * C57BL/6JJcl	N	18288644
MGI:3807083	M	MP:0005389	reproductive system phenotype	Foxs1<tm1Kmor>/Foxs1<tm1Kmor>	involves: 129P2/OlaHsd * C57BL/6JJcl	Y	18288644
MGI:3807083	M	MP:0009489	abnormal blood vessel endothelium morphology	Foxs1<tm1Kmor>/Foxs1<tm1Kmor>	involves: 129P2/OlaHsd * C57BL/6JJcl	N	18288644
MGI:3807084	M	MP:0031138	testicular hemorrhage	Foxs1<tm1Kmor>/Foxs1<+>	involves: 129P2/OlaHsd * C57BL/6JJcl	N	18288644
MGI:3807552	F	MP:0004946	abnormal regulatory T cell physiology	Foxp3<tm1.1Mal>/Foxp3<tm1.1Mal>,Lat<tm1.1Mal>/Lat<tm1.1Mal>	involves: 129S2/SvPas * C57BL/6	N	18209052
MGI:3807552	F	MP:0001823	thymus hypoplasia	Foxp3<tm1.1Mal>/Foxp3<tm1.1Mal>,Lat<tm1.1Mal>/Lat<tm1.1Mal>	involves: 129S2/SvPas * C57BL/6	N	18209052
MGI:3807552	F	MP:0004974	decreased regulatory T cell number	Foxp3<tm1.1Mal>/Foxp3<tm1.1Mal>,Lat<tm1.1Mal>/Lat<tm1.1Mal>	involves: 129S2/SvPas * C57BL/6	N	18209052
MGI:3807580	F	MP:0001386	abnormal maternal nurturing	Nr2e1<tm1Gsc>/Nr2e1<tm1Gsc>	involves: 129 * C57BL/6	N	9394001
MGI:3807712	M	MP:0001925	male infertility	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	N	18453535
MGI:3807712	M	MP:0008892	abnormal sperm flagellum morphology	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	N	18453535
MGI:3807712	M	MP:0009230	abnormal sperm head morphology	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	N	18453535
MGI:3807712	M	MP:0002687	oligozoospermia	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	N	18453535
MGI:3807712	M	MP:0003698	abnormal male reproductive system physiology	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	N	18453535
MGI:3807712	M	MP:0009852	increased Sertoli cell phagocytosis	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	N	18453535
MGI:3807712	M	MP:0005376	homeostasis/metabolism phenotype	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	Y	18453535
MGI:3807712	M	MP:0006380	abnormal spermatid morphology	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	N	18453535
MGI:3807713	M	MP:0005378	growth/size/body region phenotype	Rsph1<tm1Htan>/Rsph1<+>	involves: 129S1/Sv * C57BL/6J	Y	18453535
MGI:3807713	M	MP:0005389	reproductive system phenotype	Rsph1<tm1Htan>/Rsph1<+>	involves: 129S1/Sv * C57BL/6J	Y	18453535
MGI:3807918	M	MP:0001146	abnormal testis morphology	Efemp1<tm2Lmar>/Efemp1<tm2Lmar>	involves: 129X1/SvJ * C57BL/6	N	17872905
MGI:3807918	F	MP:0001120	abnormal uterus morphology	Efemp1<tm2Lmar>/Efemp1<tm2Lmar>	involves: 129X1/SvJ * C57BL/6	N	17872905
MGI:3807961	M	MP:0002376	abnormal dendritic cell physiology	Irak1<tm1Jth>/Y,Irak2<tm1Aki>/Irak2<tm1Aki>	involves: 129/Sv * C57BL/6	N	18438411
MGI:3807961	M	MP:0008734	decreased susceptibility to endotoxin shock	Irak1<tm1Jth>/Y,Irak2<tm1Aki>/Irak2<tm1Aki>	involves: 129/Sv * C57BL/6	N	18438411
MGI:3807961	M	MP:0002451	abnormal macrophage physiology	Irak1<tm1Jth>/Y,Irak2<tm1Aki>/Irak2<tm1Aki>	involves: 129/Sv * C57BL/6	N	18438411
MGI:3807979	F	MP:0002576	abnormal enamel morphology	Amelx<Rgsc888>/Amelx<+>	involves: C57BL/6JJcl * DBA/2JJcl	N	MGI:3778963
MGI:3808007	M	MP:0001147	small testis	Pth2<tm1Vlcg>/Pth2<tm1Vlcg>	involves: 129 * C57BL/6	N	18483145
MGI:3808007	M	MP:0004910	decreased seminal vesicle weight	Pth2<tm1Vlcg>/Pth2<tm1Vlcg>	involves: 129 * C57BL/6	N	18483145
MGI:3808007	F	MP:0001926	female infertility	Pth2<tm1Vlcg>/Pth2<tm1Vlcg>	involves: 129 * C57BL/6	N	18483145
MGI:3808007	F	MP:0001127	small ovary	Pth2<tm1Vlcg>/Pth2<tm1Vlcg>	involves: 129 * C57BL/6	N	18483145
MGI:3808007	F	MP:0001119	abnormal female reproductive system morphology	Pth2<tm1Vlcg>/Pth2<tm1Vlcg>	involves: 129 * C57BL/6	N	18483145
MGI:3808007	M	MP:0001146	abnormal testis morphology	Pth2<tm1Vlcg>/Pth2<tm1Vlcg>	involves: 129 * C57BL/6	N	18483145
MGI:3808007	F	MP:0002777	absent ovarian follicles	Pth2<tm1Vlcg>/Pth2<tm1Vlcg>	involves: 129 * C57BL/6	N	18483145
MGI:3808007	M	MP:0006380	abnormal spermatid morphology	Pth2<tm1Vlcg>/Pth2<tm1Vlcg>	involves: 129 * C57BL/6	N	18483145
MGI:3808007	M	MP:0004852	decreased testis weight	Pth2<tm1Vlcg>/Pth2<tm1Vlcg>	involves: 129 * C57BL/6	N	18483145
MGI:3808007	M	MP:0001145	abnormal male reproductive system morphology	Pth2<tm1Vlcg>/Pth2<tm1Vlcg>	involves: 129 * C57BL/6	N	18483145
MGI:3808007	M	MP:0001925	male infertility	Pth2<tm1Vlcg>/Pth2<tm1Vlcg>	involves: 129 * C57BL/6	N	18483145
MGI:3808008	F	MP:0001926	female infertility	Pth2<tm1Vlcg>/Pth2<tm1Vlcg>,Tg(CAG-LacZ,-Pth2)1Tbu/0,Tg(Prm-cre)58Og/0	involves: 129 * C57BL/6	N	18483145
MGI:3808134	M	MP:0005578	teratozoospermia	Cstf2t<tm1Ccma>/Cstf2t<tm1Ccma>	involves: 129S/SvEv * C57BL/6	N	18077340
MGI:3808134	M	MP:0001932	abnormal spermiogenesis	Cstf2t<tm1Ccma>/Cstf2t<tm1Ccma>	involves: 129S/SvEv * C57BL/6	N	18077340
MGI:3808134	M	MP:0002686	globozoospermia	Cstf2t<tm1Ccma>/Cstf2t<tm1Ccma>	involves: 129S/SvEv * C57BL/6	N	18077340
MGI:3808134	M	MP:0002675	asthenozoospermia	Cstf2t<tm1Ccma>/Cstf2t<tm1Ccma>	involves: 129S/SvEv * C57BL/6	N	18077340
MGI:3808134	M	MP:0006380	abnormal spermatid morphology	Cstf2t<tm1Ccma>/Cstf2t<tm1Ccma>	involves: 129S/SvEv * C57BL/6	N	18077340
MGI:3808134	M	MP:0001925	male infertility	Cstf2t<tm1Ccma>/Cstf2t<tm1Ccma>	involves: 129S/SvEv * C57BL/6	N	18077340
MGI:3808134	M	MP:0004182	abnormal spermiation	Cstf2t<tm1Ccma>/Cstf2t<tm1Ccma>	involves: 129S/SvEv * C57BL/6	N	18077340
MGI:3808134	M	MP:0002687	oligozoospermia	Cstf2t<tm1Ccma>/Cstf2t<tm1Ccma>	involves: 129S/SvEv * C57BL/6	N	18077340
MGI:3808613	M	MP:0009736	abnormal prostate gland branching morphogenesis	Sfrp1<tm1Jrbn>/Sfrp1<tm1Jrbn>	involves: 129 * C57BL/6J	N	18371946
MGI:3808613	M	MP:0001158	abnormal prostate gland morphology	Sfrp1<tm1Jrbn>/Sfrp1<tm1Jrbn>	involves: 129 * C57BL/6J	N	18371946
MGI:3808614	M	MP:0001158	abnormal prostate gland morphology	Tg(Pbsn-SFRP1)1Pcma/0	FVB/N-Tg(Pbsn-SFRP1)1Pcma	N	18371946
MGI:3808727	M	MP:0004543	abnormal sperm physiology	Crisp1<tm1Pasc>/Crisp1<tm1Pasc>	involves: 129S6/SvEvTac * C57BL/6N	N	18571638
MGI:3808846	F	MP:0014347	increased spleen B cell follicle size	Fen1<tm2Klng>/Fen1<tm2Klng>	involves: 129X1/SvJ * C57BL/6	N	18559501
MGI:3808846	F	MP:0014262	increased spleen B cell follicle number	Fen1<tm2Klng>/Fen1<tm2Klng>	involves: 129X1/SvJ * C57BL/6	N	18559501
MGI:3808846	F	MP:0008470	abnormal spleen B cell follicle morphology	Fen1<tm2Klng>/Fen1<tm2Klng>	involves: 129X1/SvJ * C57BL/6	N	18559501
MGI:3808878	F	MP:0001923	reduced female fertility	Ikbkg<m1Btlr>/Ikbkg<+>	C57BL/6J-Ikbkg<m1Btlr>	N	MGI:3808708
MGI:3808880	M	MP:0004974	decreased regulatory T cell number	Ikbkg<m1Btlr>/Y	C57BL/6J-Ikbkg<m1Btlr>	N	MGI:3808708
MGI:3808880	M	MP:0010768	mortality/aging	Ikbkg<m1Btlr>/Y	C57BL/6J-Ikbkg<m1Btlr>	Y	MGI:3808708
MGI:3808880	M	MP:0005387	immune system phenotype	Ikbkg<m1Btlr>/Y	C57BL/6J-Ikbkg<m1Btlr>	Y	MGI:3808708
MGI:3808880	M	MP:0008561	decreased tumor necrosis factor secretion	Ikbkg<m1Btlr>/Y	C57BL/6J-Ikbkg<m1Btlr>	N	MGI:3808708
MGI:3808880	M	MP:0005159	azoospermia	Ikbkg<m1Btlr>/Y	C57BL/6J-Ikbkg<m1Btlr>	N	MGI:3808708
MGI:3808886	M	MP:0001148	enlarged testis	Fmr1<tm1.2Cidz>/Y	involves: 129P2/OlaHsd * C57BL/6	N	16257225
MGI:3809311	F	MP:0003582	abnormal ovary development	Tmprss6<tm1Otin>/Tmprss6<tm1Otin>	involves: 129P2/OlaHsd * C57BL/6J	N	18523150
MGI:3809311	F	MP:0001926	female infertility	Tmprss6<tm1Otin>/Tmprss6<tm1Otin>	involves: 129P2/OlaHsd * C57BL/6J	N	18523150
MGI:3809399	F	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	B6.129S6-Sh2d1a<tm1Pls>	N	15539156
MGI:3809399	F	MP:0002492	decreased IgE level	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	B6.129S6-Sh2d1a<tm1Pls>	N	15539156
MGI:3809400	F	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology	Sh2d1a<tm1Vei>/Sh2d1a<tm1Vei>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15539156
MGI:3809400	F	MP:0002492	decreased IgE level	Sh2d1a<tm1Vei>/Sh2d1a<tm1Vei>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15539156
MGI:3809400	F	MP:0008051	abnormal memory T cell physiology	Sh2d1a<tm1Vei>/Sh2d1a<tm1Vei>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15539156
MGI:3809483	M	MP:0010771	integument phenotype	Dkc1<tm1.1Pjma>/Y	involves: 129X1/SvJ * C57BL/6 * FVB/N	Y	18626023
MGI:3809483	M	MP:0008058	abnormal DNA repair	Dkc1<tm1.1Pjma>/Y	involves: 129X1/SvJ * C57BL/6 * FVB/N	N	18626023
MGI:3809483	M	MP:0005397	hematopoietic system phenotype	Dkc1<tm1.1Pjma>/Y	involves: 129X1/SvJ * C57BL/6 * FVB/N	Y	18626023
MGI:3809484	F	MP:0002396	abnormal hematopoietic system morphology/development	Dkc1<tm1.1Pjma>/Dkc1<+>	involves: 129X1/SvJ * C57BL/6 * FVB/N	N	18626023
MGI:3809646	M	MP:0002687	oligozoospermia	Sgo2a<Gt(D025B05)Wrst>/Sgo2a<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	N	18765791
MGI:3809646	M	MP:0008261	arrest of male meiosis	Sgo2a<Gt(D025B05)Wrst>/Sgo2a<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	N	18765791
MGI:3809646	F	MP:0001926	female infertility	Sgo2a<Gt(D025B05)Wrst>/Sgo2a<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	N	18765791
MGI:3809646	M	MP:0001147	small testis	Sgo2a<Gt(D025B05)Wrst>/Sgo2a<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	N	18765791
MGI:3809646	F	MP:0005168	abnormal female meiosis	Sgo2a<Gt(D025B05)Wrst>/Sgo2a<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	N	18765791
MGI:3809646	M	MP:0001925	male infertility	Sgo2a<Gt(D025B05)Wrst>/Sgo2a<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	N	18765791
MGI:3809646	M	MP:0006380	abnormal spermatid morphology	Sgo2a<Gt(D025B05)Wrst>/Sgo2a<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	N	18765791
MGI:3809702	F	MP:0001923	reduced female fertility	Mirc55<tm1.1Eno>/Mirc55<tm1.1Eno>	Not Specified	N	18694565
MGI:3809765	M	MP:0008973	decreased erythroid progenitor cell number	Gata1<tm10Sho>/Y	involves: C57BL/6	N	16391009
MGI:3809765	M	MP:0005397	hematopoietic system phenotype	Gata1<tm10Sho>/Y	involves: C57BL/6	Y	16391009
MGI:3809766	M	MP:0005397	hematopoietic system phenotype	Gata1<tm9Sho>/Y	involves: C57BL/6	Y	16391009
MGI:3809793	F	MP:0005389	reproductive system phenotype	Xiap<tm1Hs>/Xiap<tm1Hs>	B6.129P2-Xiap<tm1Hs>	Y	18708583
MGI:3809793	F	MP:0008943	increased sensitivity to induced cell death	Xiap<tm1Hs>/Xiap<tm1Hs>	B6.129P2-Xiap<tm1Hs>	N	18708583
MGI:3809793	F	MP:0005387	immune system phenotype	Xiap<tm1Hs>/Xiap<tm1Hs>	B6.129P2-Xiap<tm1Hs>	Y	18708583
MGI:3809794	F	MP:0008782	increased B cell apoptosis	Tg(IghMyc)22Bri/0,Xiap<tm1Hs>/Xiap<tm1Hs>	B6.Cg-Xiap<tm1Hs> Tg(IghMyc)22Bri	N	18708583
MGI:3809794	F	MP:0005093	decreased B cell proliferation	Tg(IghMyc)22Bri/0,Xiap<tm1Hs>/Xiap<tm1Hs>	B6.Cg-Xiap<tm1Hs> Tg(IghMyc)22Bri	N	18708583
MGI:3809794	F	MP:0000221	decreased leukocyte cell number	Tg(IghMyc)22Bri/0,Xiap<tm1Hs>/Xiap<tm1Hs>	B6.Cg-Xiap<tm1Hs> Tg(IghMyc)22Bri	N	18708583
MGI:3809794	F	MP:0010768	mortality/aging	Tg(IghMyc)22Bri/0,Xiap<tm1Hs>/Xiap<tm1Hs>	B6.Cg-Xiap<tm1Hs> Tg(IghMyc)22Bri	Y	18708583
MGI:3809827	F	MP:0001926	female infertility	Lbr<Gt(XE569)Byg>/Lbr<Gt(XE569)Byg>	involves: 129P2/OlaHsd * C57BL/6Cr	N	18621876
MGI:3809827	F	MP:0001121	uterus hypoplasia	Lbr<Gt(XE569)Byg>/Lbr<Gt(XE569)Byg>	involves: 129P2/OlaHsd * C57BL/6Cr	N	18621876
MGI:3809827	M	MP:0001925	male infertility	Lbr<Gt(XE569)Byg>/Lbr<Gt(XE569)Byg>	involves: 129P2/OlaHsd * C57BL/6Cr	N	18621876
MGI:3810123	F	MP:0002945	abnormal inhibitory postsynaptic currents	Glra2<tm1Lex>/Glra2<tm1Lex>	Not Specified	N	17920294
MGI:3810123	F	MP:0010768	mortality/aging	Glra2<tm1Lex>/Glra2<tm1Lex>	Not Specified	Y	17920294
MGI:3810123	F	MP:0005389	reproductive system phenotype	Glra2<tm1Lex>/Glra2<tm1Lex>	Not Specified	Y	17920294
MGI:3810123	F	MP:0005378	growth/size/body region phenotype	Glra2<tm1Lex>/Glra2<tm1Lex>	Not Specified	Y	17920294
MGI:3810148	M	MP:0008261	arrest of male meiosis	Stra8<tm1.1Nbg>/Stra8<tm1.1Nbg>	involves: 129S2/SvPas * C57BL/6	N	18799790
MGI:3810148	M	MP:0005169	abnormal male meiosis	Stra8<tm1.1Nbg>/Stra8<tm1.1Nbg>	involves: 129S2/SvPas * C57BL/6	N	18799790
MGI:3810148	F	MP:0004805	absent oocytes	Stra8<tm1.1Nbg>/Stra8<tm1.1Nbg>	involves: 129S2/SvPas * C57BL/6	N	18799790
MGI:3810148	F	MP:0001132	absent mature ovarian follicles	Stra8<tm1.1Nbg>/Stra8<tm1.1Nbg>	involves: 129S2/SvPas * C57BL/6	N	18799790
MGI:3810148	M	MP:0005159	azoospermia	Stra8<tm1.1Nbg>/Stra8<tm1.1Nbg>	involves: 129S2/SvPas * C57BL/6	N	18799790
MGI:3810254	F	MP:0005391	vision/eye phenotype	Arr3<tm1Chcr>/Arr3<tm1Chcr>	involves: 129S/SvEv * C57BL/6	Y	18701071
MGI:3810255	F	MP:0004022	abnormal cone electrophysiology	Arr3<tm1Chcr>/Arr3<tm1Chcr>,Sag<tm1Jnc>/Sag<tm1Jnc>	involves: 129S/SvEv * C57BL/6	N	18701071
MGI:3810333	F	MP:0005377	hearing/vestibular/ear phenotype	Hprt1<tm2Brd>/Hprt1<+>,Myo7a<4626SB>/Myo7a<4626SB>	involves: 129S7/SvEvBrd * BALB/cRl * C3H * C57BL/6J * CBA/Ca	Y	18160714
MGI:3810334	F	MP:0005377	hearing/vestibular/ear phenotype	Hprt1<tm3Brd>/Hprt1<+>,Myo7a<4626SB>/Myo7a<4626SB>	involves: 129S7/SvEvBrd * BALB/cRl * C3H * C57BL/6J * CBA/Ca	Y	18160714
MGI:3810338	M	MP:0005386	behavior/neurological phenotype	Hprt1<b-m1>/Y	involves: 129S/SvEv	Y	1528024
MGI:3810338	M	MP:0005386	behavior/neurological phenotype	Hprt1<b-m1>/Y	involves: 129S/SvEv	Y	3029599
MGI:3810339	M	MP:0005386	behavior/neurological phenotype	Hprt1<b-m2>/Y	involves: 129S/SvEv	Y	1528024
MGI:3810339	M	MP:0005386	behavior/neurological phenotype	Hprt1<b-m2>/Y	involves: 129S/SvEv	Y	3029599
MGI:3810360	M	MP:0005386	behavior/neurological phenotype	Hprt1<b-m1>/Y	involves: 129 * 129S/SvEv	Y	3221240
MGI:3810360	M	MP:0002757	decreased vertical activity	Hprt1<b-m1>/Y	involves: 129 * 129S/SvEv	N	3221240
MGI:3810360	M	MP:0005643	decreased dopamine level	Hprt1<b-m1>/Y	involves: 129 * 129S/SvEv	N	3221240
MGI:3810360	M	MP:0001516	abnormal motor coordination/balance	Hprt1<b-m1>/Y	involves: 129 * 129S/SvEv	N	3221240
MGI:3810361	M	MP:0003313	abnormal locomotor activation	Hprt1<b-m2>/Y	involves: 129 * 129S/SvEv	N	3221240
MGI:3810361	M	MP:0005386	behavior/neurological phenotype	Hprt1<b-m2>/Y	involves: 129 * 129S/SvEv	Y	3221240
MGI:3810361	M	MP:0001516	abnormal motor coordination/balance	Hprt1<b-m2>/Y	involves: 129 * 129S/SvEv	N	3221240
MGI:3810361	M	MP:0005643	decreased dopamine level	Hprt1<b-m2>/Y	involves: 129 * 129S/SvEv	N	3221240
MGI:3810482	M	MP:0006362	abnormal male germ cell morphology	Fshr<tm1Saco>/Fshr<+>	involves: C57BL/6	N	10775161
MGI:3810482	M	MP:0004543	abnormal sperm physiology	Fshr<tm1Saco>/Fshr<+>	involves: C57BL/6	N	10775161
MGI:3810482	F	MP:0001127	small ovary	Fshr<tm1Saco>/Fshr<+>	involves: C57BL/6	N	9811848
MGI:3810482	M	MP:0001932	abnormal spermiogenesis	Fshr<tm1Saco>/Fshr<+>	involves: C57BL/6	N	10775161
MGI:3810482	F	MP:0002637	small uterus	Fshr<tm1Saco>/Fshr<+>	involves: C57BL/6	N	9811848
MGI:3810482	M	MP:0001922	reduced male fertility	Fshr<tm1Saco>/Fshr<+>	involves: C57BL/6	N	9811848
MGI:3810482	F	MP:0001923	reduced female fertility	Fshr<tm1Saco>/Fshr<+>	involves: C57BL/6	N	9811848
MGI:3810483	F	MP:0008000	increased ovary tumor incidence	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0001927	abnormal estrous cycle	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0011125	decreased primary ovarian follicle number	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0009433	polyovular ovarian follicle	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0009093	oocyte degeneration	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0009016	abnormal estrus	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	11089565
MGI:3810483	F	MP:0009011	prolonged diestrus	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	11089565
MGI:3810483	F	MP:0001134	absent corpus luteum	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0009009	absent estrous cycle	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0009006	prolonged estrous cycle	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0009006	prolonged estrous cycle	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	11089565
MGI:3810483	F	MP:0008871	abnormal ovarian follicle number	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0008868	abnormal granulosa cell morphology	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0006361	abnormal female germ cell morphology	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0002016	ovary cyst	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	11459817
MGI:3810483	F	MP:0002016	ovary cyst	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0001926	female infertility	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	11089565
MGI:3810483	F	MP:0001923	reduced female fertility	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0004805	absent oocytes	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0001130	abnormal ovarian folliculogenesis	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0002293	long gestation period	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0003507	abnormal ovary physiology	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810483	F	MP:0002678	increased follicle recruitment	Fshr<tm1Saco>/Fshr<+>	involves: 129	N	12135868
MGI:3810495	F	MP:0000160	kyphosis	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	M	MP:0002685	abnormal spermatogonia proliferation	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11466221
MGI:3810495	F	MP:0001140	abnormal vagina epithelium morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0008908	increased total fat pad weight	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0004856	decreased ovary weight	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0001505	hunched posture	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0020010	decreased bone mineral density of femur	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0004895	vagina atrophy	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	M	MP:0001932	abnormal spermiogenesis	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11466221
MGI:3810495	M	MP:0002687	oligozoospermia	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	15973687
MGI:3810495	F	MP:0004894	uterus atrophy	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0001260	increased body weight	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0001120	abnormal uterus morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0003529	enlarged clitoris	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	M	MP:0009248	small caput epididymis	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	15973687
MGI:3810495	F	MP:0008980	decreased vagina weight	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0002781	increased circulating testosterone level	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	M	MP:0008975	delayed male fertility	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11466221
MGI:3810495	F	MP:0009081	thin uterus	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	M	MP:0004929	decreased epididymis weight	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11466221
MGI:3810495	M	MP:0009230	abnormal sperm head morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	15973687
MGI:3810495	F	MP:0001926	female infertility	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11459817
MGI:3810495	F	MP:0008869	anovulation	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11459817
MGI:3810495	M	MP:0006380	abnormal spermatid morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11466221
MGI:3810495	F	MP:0003579	increased ovarian carcinoma incidence	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11459817
MGI:3810495	F	MP:0003132	increased pre-B cell number	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	M	MP:0005578	teratozoospermia	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	15973687
MGI:3810495	F	MP:0001134	absent corpus luteum	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	M	MP:0002661	abnormal corpus epididymis morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	15973687
MGI:3810495	M	MP:0009838	abnormal sperm axoneme morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	15973687
MGI:3810495	F	MP:0030826	decreased femur weight	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	M	MP:0005250	decreased Sertoli cell number	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11466221
MGI:3810495	F	MP:0001134	absent corpus luteum	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11459817
MGI:3810495	F	MP:0001132	absent mature ovarian follicles	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	M	MP:0001938	delayed sexual maturation	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11466221
MGI:3810495	M	MP:0002675	asthenozoospermia	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	15973687
MGI:3810495	F	MP:0001927	abnormal estrous cycle	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0009009	absent estrous cycle	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0001129	impaired ovarian folliculogenesis	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11459817
MGI:3810495	F	MP:0009009	absent estrous cycle	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11459817
MGI:3810495	M	MP:0004933	abnormal epididymis epithelium morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	15973687
MGI:3810495	F	MP:0001261	obese	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	M	MP:0001922	reduced male fertility	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11466221
MGI:3810495	F	MP:0005181	decreased circulating estradiol level	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0005185	decreased circulating progesterone level	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0001127	small ovary	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11459817
MGI:3810495	M	MP:0009232	abnormal sperm nucleus morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	15973687
MGI:3810495	M	MP:0001935	decreased litter size	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11466221
MGI:3810495	M	MP:0003830	abnormal testis development	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11466221
MGI:3810495	M	MP:0001153	small seminiferous tubules	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11466221
MGI:3810495	M	MP:0009231	detached acrosome	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	15973687
MGI:3810495	F	MP:0009094	abnormal endometrial gland morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0009090	myometrium hypoplasia	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0001126	abnormal ovary morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	M	MP:0004852	decreased testis weight	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11466221
MGI:3810495	F	MP:0004905	decreased uterus weight	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0001142	abnormal vagina orifice morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11089565
MGI:3810495	F	MP:0002016	ovary cyst	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11459817
MGI:3810495	F	MP:0001126	abnormal ovary morphology	Fshr<tm1Saco>/Fshr<tm1Saco>	involves: 129	N	11459817
MGI:3810531	F	MP:0010768	mortality/aging	Fgf16<tm1(cre)Sms>/Fgf16<tm1(cre)Sms>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	18773497
MGI:3810531	F	MP:0005386	behavior/neurological phenotype	Fgf16<tm1(cre)Sms>/Fgf16<tm1(cre)Sms>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	18773497
MGI:3810531	F	MP:0005377	hearing/vestibular/ear phenotype	Fgf16<tm1(cre)Sms>/Fgf16<tm1(cre)Sms>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	18773497
MGI:3810531	F	MP:0005389	reproductive system phenotype	Fgf16<tm1(cre)Sms>/Fgf16<tm1(cre)Sms>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	18773497
MGI:3810533	M	MP:0005389	reproductive system phenotype	Fgf16<tm1(cre)Sms>/Y	involves: 129S1/Sv * 129X1/SvJ	Y	18773497
MGI:3810533	M	MP:0010768	mortality/aging	Fgf16<tm1(cre)Sms>/Y	involves: 129S1/Sv * 129X1/SvJ	Y	18773497
MGI:3810533	M	MP:0005377	hearing/vestibular/ear phenotype	Fgf16<tm1(cre)Sms>/Y	involves: 129S1/Sv * 129X1/SvJ	Y	18773497
MGI:3810533	M	MP:0005386	behavior/neurological phenotype	Fgf16<tm1(cre)Sms>/Y	involves: 129S1/Sv * 129X1/SvJ	Y	18773497
MGI:3810639	F	MP:0002169	no abnormal phenotype detected	Hdac6<tm1Pmt>/Hdac6<tm1Pmt>	involves: 129P2/OlaHsd * C57BL/6	N	18180281
MGI:3810640	F	MP:0005387	immune system phenotype	Hdac6<tm1.1Pmt>/Hdac6<tm1.1Pmt>	involves: 129P2/OlaHsd * C57BL/6	Y	18180281
MGI:3810640	F	MP:0003631	nervous system phenotype	Hdac6<tm1.1Pmt>/Hdac6<tm1.1Pmt>	involves: 129P2/OlaHsd * C57BL/6	Y	18180281
MGI:3810640	F	MP:0001805	decreased IgG level	Hdac6<tm1.1Pmt>/Hdac6<tm1.1Pmt>	involves: 129P2/OlaHsd * C57BL/6	N	18180281
MGI:3810640	F	MP:0001806	decreased IgM level	Hdac6<tm1.1Pmt>/Hdac6<tm1.1Pmt>	involves: 129P2/OlaHsd * C57BL/6	N	18180281
MGI:3810640	F	MP:0001260	increased body weight	Hdac6<tm1.1Pmt>/Hdac6<tm1.1Pmt>	involves: 129P2/OlaHsd * C57BL/6	N	18180281
MGI:3810640	F	MP:0005389	reproductive system phenotype	Hdac6<tm1.1Pmt>/Hdac6<tm1.1Pmt>	involves: 129P2/OlaHsd * C57BL/6	Y	18180281
MGI:3810640	F	MP:0010123	increased bone mineral content	Hdac6<tm1.1Pmt>/Hdac6<tm1.1Pmt>	involves: 129P2/OlaHsd * C57BL/6	N	18180281
MGI:3810640	F	MP:0000062	increased bone mineral density	Hdac6<tm1.1Pmt>/Hdac6<tm1.1Pmt>	involves: 129P2/OlaHsd * C57BL/6	N	18180281
MGI:3810657	F	MP:0000628	abnormal mammary gland development	Ncoa6<tm1Jkr>/Ncoa6<tm1Jkr>,Tg(MMTV-cre)FMam/?	involves: 129P2/OlaHsd * FVB	N	15161927
MGI:3810657	F	MP:0013716	hypolactation	Ncoa6<tm1Jkr>/Ncoa6<tm1Jkr>,Tg(MMTV-cre)FMam/?	involves: 129P2/OlaHsd * FVB	N	15161927
MGI:3810657	F	MP:0013782	abnormal mammary duct terminal end bud morphology	Ncoa6<tm1Jkr>/Ncoa6<tm1Jkr>,Tg(MMTV-cre)FMam/?	involves: 129P2/OlaHsd * FVB	N	15161927
MGI:3810657	F	MP:0006269	abnormal mammary gland growth during pregnancy	Ncoa6<tm1Jkr>/Ncoa6<tm1Jkr>,Tg(MMTV-cre)FMam/?	involves: 129P2/OlaHsd * FVB	N	15161927
MGI:3810657	F	MP:0006270	abnormal mammary gland growth during lactation	Ncoa6<tm1Jkr>/Ncoa6<tm1Jkr>,Tg(MMTV-cre)FMam/?	involves: 129P2/OlaHsd * FVB	N	15161927
MGI:3810657	F	MP:0000662	abnormal branching of the mammary ductal tree	Ncoa6<tm1Jkr>/Ncoa6<tm1Jkr>,Tg(MMTV-cre)FMam/?	involves: 129P2/OlaHsd * FVB	N	15161927
MGI:3810753	M	MP:0020351	decreased vocalization	Lmx1b<tm1Zfc>/Lmx1b<tm1Zfc>,Tg(Fev-cre)1Esd/0	involves: 129S7/SvEvBrd * C57BL/6 * SJL	N	21441904
MGI:3810753	M	MP:0001375	abnormal mating preference	Lmx1b<tm1Zfc>/Lmx1b<tm1Zfc>,Tg(Fev-cre)1Esd/0	involves: 129S7/SvEvBrd * C57BL/6 * SJL	N	21441904
MGI:3810763	F	MP:0001926	female infertility	Jag2<sm>/Jag2<sm>	involves: A/Fa	N	MGI:61258
MGI:3810823	F	MP:0001926	female infertility	Hoxa11<tm1Mrc>/Hoxa11<tm1Mrc>	Not Specified	N	12217321
MGI:3810823	M	MP:0001922	reduced male fertility	Hoxa11<tm1Mrc>/Hoxa11<tm1Mrc>	Not Specified	N	12217321
MGI:3810830	M	MP:0001922	reduced male fertility	Hoxa11<tm1Mrc>/Hoxa11<tm1Mrc>,Hoxd11<tm2.1(Hoxd11)Mrc>/Hoxd11<+>	involves: BALB/cJ	N	12217321
MGI:3810830	F	MP:0001926	female infertility	Hoxa11<tm1Mrc>/Hoxa11<tm1Mrc>,Hoxd11<tm2.1(Hoxd11)Mrc>/Hoxd11<+>	involves: BALB/cJ	N	12217321
MGI:3810831	M	MP:0001925	male infertility	Hoxa11<tm1Mrc>/Hoxa11<tm1Mrc>,Hoxd11<tm2.1(Hoxd11)Mrc>/Hoxd11<tm2.1(Hoxd11)Mrc>	involves: BALB/cJ	N	12217321
MGI:3810831	F	MP:0001926	female infertility	Hoxa11<tm1Mrc>/Hoxa11<tm1Mrc>,Hoxd11<tm2.1(Hoxd11)Mrc>/Hoxd11<tm2.1(Hoxd11)Mrc>	involves: BALB/cJ	N	12217321
MGI:3810946	F	MP:0004896	abnormal endometrium morphology	Hoxa11<tm2.1(Hoxa13)Ssp>/Hoxa11<tm2.1(Hoxa13)Ssp>	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	N	11688568
MGI:3810946	F	MP:0001926	female infertility	Hoxa11<tm2.1(Hoxa13)Ssp>/Hoxa11<tm2.1(Hoxa13)Ssp>	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	N	11688568
MGI:3810946	F	MP:0009097	absent endometrial glands	Hoxa11<tm2.1(Hoxa13)Ssp>/Hoxa11<tm2.1(Hoxa13)Ssp>	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	N	11688568
MGI:3810947	F	MP:0001926	female infertility	Hoxa11<tm2.1(Hoxa13)Ssp>/Hoxa11<+>	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	N	11688568
MGI:3810947	F	MP:0009097	absent endometrial glands	Hoxa11<tm2.1(Hoxa13)Ssp>/Hoxa11<+>	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	N	11688568
MGI:3810948	F	MP:0001926	female infertility	Hoxa11<tm1Ssp>/Hoxa11<tm2.1(Hoxa13)Ssp>,Hoxd11<tm1Mrc>/Hoxd11<+>	either: (involves: 129P2/OlaHsd * 129S2/SvPas * 129S7/SvEvBrd) or (involves: 129S1/Sv * 129S2/SvPas * 129S7/SvEvBrd * 129X1/SvJ)	N	11688568
MGI:3810949	F	MP:0001926	female infertility	Hoxa11<tm1Ssp>/Hoxa11<tm2.1(Hoxa13)Ssp>,Hoxd11<tm1Mrc>/Hoxd11<tm1Mrc>	either: (involves: 129P2/OlaHsd * 129S2/SvPas * 129S7/SvEvBrd) or (involves: 129S1/Sv * 129S2/SvPas * 129S7/SvEvBrd * 129X1/SvJ)	N	11688568
MGI:3810951	F	MP:0009096	decreased endometrial gland number	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>	involves: 129S2/SvPas	N	11688568
MGI:3810951	F	MP:0008258	thin endometrium	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>	involves: 129S2/SvPas	N	11688568
MGI:3810951	M	MP:0002769	abnormal vas deferens morphology	Hoxa11<tm1Ssp>/Hoxa11<tm1Ssp>	involves: 129S2/SvPas	N	11688568
MGI:3810952	F	MP:0001926	female infertility	Hoxa11<tm1Ssp>/Hoxa11<tm2.1(Hoxa13)Ssp>	either: (involves: 129P2/OlaHsd * 129S2/SvPas) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)	N	11688568
MGI:3810954	M	MP:0008985	hemimelia	Xpl/Y	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	7391545
MGI:3810954	M	MP:0001925	male infertility	Xpl/Y	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	7391545
MGI:3810954	M	MP:0008985	hemimelia	Xpl/Y	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	MGI:72480
MGI:3810954	M	MP:0000562	polydactyly	Xpl/Y	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	7391545
MGI:3810954	M	MP:0000520	absent kidney	Xpl/Y	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	7391545
MGI:3810954	M	MP:0000519	hydronephrosis	Xpl/Y	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	7391545
MGI:3810954	M	MP:0003675	kidney cyst	Xpl/Y	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	7391545
MGI:3810954	M	MP:0000536	hydroureter	Xpl/Y	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	7391545
MGI:3810954	M	MP:0002286	cryptorchism	Xpl/Y	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	7391545
MGI:3810954	M	MP:0000562	polydactyly	Xpl/Y	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	MGI:72480
MGI:3810955	F	MP:0008985	hemimelia	Xpl/Xpl<+>	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	7391545
MGI:3810955	F	MP:0000562	polydactyly	Xpl/Xpl<+>	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	7391545
MGI:3810955	F	MP:0000562	polydactyly	Xpl/Xpl<+>	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	MGI:72480
MGI:3810955	F	MP:0008985	hemimelia	Xpl/Xpl<+>	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	MGI:72480
MGI:3810964	F	MP:0000562	polydactyly	Xpl/Xpl	involves: C3HeB/FeJ * C57BL/6J * English fancy stock	N	7391545
MGI:3810967	F	MP:0001729	impaired embryo implantation	Ptpn11<tm5Bgn>/Ptpn11<tm5Bgn>	involves: 129S4/SvJae * C57BL/6J	N	16516835
MGI:3811008	M	MP:0012528	abnormal zone of polarizing activity morphology	Xpl/Y	involves: C57BL/6J * MSM	N	9073443
MGI:3811009	F	MP:0012528	abnormal zone of polarizing activity morphology	Xpl/Xpl<+>	involves: C57BL/6J * MSM	N	9073443
MGI:3811038	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>	involves: 129S1/Sv	N	18245377
MGI:3811039	M	MP:0000666	decreased prostate gland duct number	Fem1b<tm1Mms>/Fem1b<tm1Mms>	either: 129S6/SvEvTac-Fem1b<tm1Mms> or (involves: 129S6/SvEvTac * C57BL/6)	N	18816836
MGI:3811150	F	MP:0001120	abnormal uterus morphology	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	12193578
MGI:3811150	F	MP:0004898	uterine hemorrhage	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	12193578
MGI:3811150	F	MP:0009009	absent estrous cycle	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	12193578
MGI:3811150	F	MP:0004833	ovary atrophy	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	14502087
MGI:3811150	F	MP:0001923	reduced female fertility	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	12193578
MGI:3811150	F	MP:0002016	ovary cyst	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	12193578
MGI:3811150	F	MP:0009251	enlarged endometrial glands	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	12193578
MGI:3811150	F	MP:0002016	ovary cyst	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	14502087
MGI:3811150	F	MP:0001126	abnormal ovary morphology	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	14502087
MGI:3811150	F	MP:0004904	increased uterus weight	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	12193578
MGI:3811150	F	MP:0004014	abnormal uterine environment	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	12193578
MGI:3811150	F	MP:0001134	absent corpus luteum	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	14502087
MGI:3811150	F	MP:0004906	enlarged uterus	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	12193578
MGI:3811150	F	MP:0009222	increased uterus tumor incidence	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	12193578
MGI:3811150	F	MP:0009221	uterus adenomyosis	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	12193578
MGI:3811150	F	MP:0009082	uterus cyst	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	12193578
MGI:3811150	F	MP:0002777	absent ovarian follicles	Fshr<tm1Saco>/Fshr<+>	involves: 129T2/SvEmsJ	N	14502087
MGI:3811198	F	MP:0002462	abnormal granulocyte physiology	Mir223<tm1Fcam>/Mir223<tm1Fcam>	involves: 129S4/SvJae * C57BL/6	N	18278031
MGI:3811198	F	MP:0000219	increased neutrophil cell number	Mir223<tm1Fcam>/Mir223<tm1Fcam>	involves: 129S4/SvJae * C57BL/6	N	18278031
MGI:3811198	F	MP:0000322	increased granulocyte number	Mir223<tm1Fcam>/Mir223<tm1Fcam>	involves: 129S4/SvJae * C57BL/6	N	18278031
MGI:3811198	F	MP:0002415	abnormal neutrophil differentiation	Mir223<tm1Fcam>/Mir223<tm1Fcam>	involves: 129S4/SvJae * C57BL/6	N	18278031
MGI:3811198	F	MP:0002463	abnormal neutrophil physiology	Mir223<tm1Fcam>/Mir223<tm1Fcam>	involves: 129S4/SvJae * C57BL/6	N	18278031
MGI:3811198	F	MP:0001861	lung inflammation	Mir223<tm1Fcam>/Mir223<tm1Fcam>	involves: 129S4/SvJae * C57BL/6	N	18278031
MGI:3811198	F	MP:0005088	increased acute inflammation	Mir223<tm1Fcam>/Mir223<tm1Fcam>	involves: 129S4/SvJae * C57BL/6	N	18278031
MGI:3811199	F	MP:0002463	abnormal neutrophil physiology	Mef2c<tm1Jjs>/Mef2c<tm1Jjs>,Mir223<tm1Fcam>/Mir223<tm1Fcam>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	involves: 129 * C57BL/6	N	18278031
MGI:3811199	F	MP:0000219	increased neutrophil cell number	Mef2c<tm1Jjs>/Mef2c<tm1Jjs>,Mir223<tm1Fcam>/Mir223<tm1Fcam>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	involves: 129 * C57BL/6	N	18278031
MGI:3811199	F	MP:0002415	abnormal neutrophil differentiation	Mef2c<tm1Jjs>/Mef2c<tm1Jjs>,Mir223<tm1Fcam>/Mir223<tm1Fcam>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	involves: 129 * C57BL/6	N	18278031
MGI:3811204	F	MP:0005459	decreased percent body fat/body weight	Gpr50<tm1Dgen>/Gpr50<tm1Dgen>	involves: C57BL/6	N	17957037
MGI:3811204	F	MP:0002089	abnormal postnatal growth/weight/body size	Gpr50<tm1Dgen>/Gpr50<tm1Dgen>	involves: C57BL/6	N	17957037
MGI:3811204	F	MP:0011939	increased food intake	Gpr50<tm1Dgen>/Gpr50<tm1Dgen>	involves: C57BL/6	N	17957037
MGI:3811204	F	MP:0005289	increased oxygen consumption	Gpr50<tm1Dgen>/Gpr50<tm1Dgen>	involves: C57BL/6	N	17957037
MGI:3811204	F	MP:0005659	decreased susceptibility to diet-induced obesity	Gpr50<tm1Dgen>/Gpr50<tm1Dgen>	involves: C57BL/6	N	17957037
MGI:3811204	F	MP:0008963	increased carbon dioxide production	Gpr50<tm1Dgen>/Gpr50<tm1Dgen>	involves: C57BL/6	N	17957037
MGI:3811204	F	MP:0008489	slow postnatal weight gain	Gpr50<tm1Dgen>/Gpr50<tm1Dgen>	involves: C57BL/6	N	17957037
MGI:3811204	F	MP:0001399	hyperactivity	Gpr50<tm1Dgen>/Gpr50<tm1Dgen>	involves: C57BL/6	N	17957037
MGI:3811275	M	MP:0001925	male infertility	Ldhc<tm1Erg>/Ldhc<tm1Erg>	involves: 129S6/SvEvTac * C57BL/6N	N	18367675
MGI:3811275	M	MP:0004543	abnormal sperm physiology	Ldhc<tm1Erg>/Ldhc<tm1Erg>	involves: 129S6/SvEvTac * C57BL/6N	N	18367675
MGI:3811275	M	MP:0004884	abnormal testis physiology	Ldhc<tm1Erg>/Ldhc<tm1Erg>	involves: 129S6/SvEvTac * C57BL/6N	N	18367675
MGI:3811275	M	MP:0002675	asthenozoospermia	Ldhc<tm1Erg>/Ldhc<tm1Erg>	involves: 129S6/SvEvTac * C57BL/6N	N	18367675
MGI:3811275	M	MP:0001922	reduced male fertility	Ldhc<tm1Erg>/Ldhc<tm1Erg>	involves: 129S6/SvEvTac * C57BL/6N	N	18367675
MGI:3811355	M	MP:0002451	abnormal macrophage physiology	Tlr7<rsq2>/Y	C57BL/6J-Tlr7<rsq2>	N	MGI:3811352
MGI:3811355	M	MP:0008561	decreased tumor necrosis factor secretion	Tlr7<rsq2>/Y	C57BL/6J-Tlr7<rsq2>	N	MGI:3811352
MGI:3811495	F	MP:0001935	decreased litter size	Tex11<tm1Jw>/Tex11<tm1Jw>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	18316482
MGI:3811495	F	MP:0008966	abnormal chiasmata formation	Tex11<tm1Jw>/Tex11<tm1Jw>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	18316482
MGI:3811496	M	MP:0008261	arrest of male meiosis	Tex11<tm1Jw>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	18316482
MGI:3811496	M	MP:0001925	male infertility	Tex11<tm1Jw>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	18316482
MGI:3811496	M	MP:0004852	decreased testis weight	Tex11<tm1Jw>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	18316482
MGI:3811496	M	MP:0008966	abnormal chiasmata formation	Tex11<tm1Jw>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	18316482
MGI:3811496	M	MP:0004218	meiotic nondisjunction during M1 phase	Tex11<tm1Jw>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	18316482
MGI:3811496	M	MP:0014052	increased male germ cell apoptosis	Tex11<tm1Jw>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	18316482
MGI:3811522	M	MP:0001925	male infertility	Bmp5<se>/Bmp5<se>,Bmp6<tm1Rob>/Bmp6<tm1Rob>	involves: 129S/SvEv	N	9664685
MGI:3811643	F	MP:0001923	reduced female fertility	Tg(Msx2-nog)14Blh/0	involves: C57BL/6 * CD-1 * DBA/2	N	11118201
MGI:3811650	M	MP:0002834	decreased heart weight	Fgf16<tm1Nit>/Y	C57BL/6-Fgf16<tm1Nit>	N	18816849
MGI:3811650	M	MP:0003567	abnormal fetal cardiomyocyte proliferation	Fgf16<tm1Nit>/Y	C57BL/6-Fgf16<tm1Nit>	N	18816849
MGI:3811650	M	MP:0003921	abnormal heart left ventricle morphology	Fgf16<tm1Nit>/Y	C57BL/6-Fgf16<tm1Nit>	N	18816849
MGI:3811650	M	MP:0002740	heart hypoplasia	Fgf16<tm1Nit>/Y	C57BL/6-Fgf16<tm1Nit>	N	18816849
MGI:3811736	F	MP:0001127	small ovary	Tex12<tm1Hoog>/Tex12<tm1Hoog>	involves: 129S2/SvPas	N	18611960
MGI:3811736	F	MP:0005168	abnormal female meiosis	Tex12<tm1Hoog>/Tex12<tm1Hoog>	involves: 129S2/SvPas	N	18611960
MGI:3811736	F	MP:0001926	female infertility	Tex12<tm1Hoog>/Tex12<tm1Hoog>	involves: 129S2/SvPas	N	18611960
MGI:3811736	F	MP:0005431	decreased oocyte number	Tex12<tm1Hoog>/Tex12<tm1Hoog>	involves: 129S2/SvPas	N	18611960
MGI:3811736	M	MP:0005169	abnormal male meiosis	Tex12<tm1Hoog>/Tex12<tm1Hoog>	involves: 129S2/SvPas	N	18611960
MGI:3811736	M	MP:0001925	male infertility	Tex12<tm1Hoog>/Tex12<tm1Hoog>	involves: 129S2/SvPas	N	18611960
MGI:3811736	F	MP:0011122	absent primordial ovarian follicles	Tex12<tm1Hoog>/Tex12<tm1Hoog>	involves: 129S2/SvPas	N	18611960
MGI:3811736	M	MP:0001155	arrest of spermatogenesis	Tex12<tm1Hoog>/Tex12<tm1Hoog>	involves: 129S2/SvPas	N	18611960
MGI:3811736	F	MP:0002777	absent ovarian follicles	Tex12<tm1Hoog>/Tex12<tm1Hoog>	involves: 129S2/SvPas	N	18611960
MGI:3811736	F	MP:0009093	oocyte degeneration	Tex12<tm1Hoog>/Tex12<tm1Hoog>	involves: 129S2/SvPas	N	18611960
MGI:3811794	M	MP:0011410	ectopic testis	Foxc1<ch>/Foxc1<ch>	involves: CBA * STOCK Tyr<c> f	N	5500588
MGI:3811794	F	MP:0011727	ectopic ovary	Foxc1<ch>/Foxc1<ch>	involves: CBA * STOCK Tyr<c> f	N	5500588
MGI:3811826	F	MP:0001882	abnormal lactation	Hr<rh>/Hr<rh>	Not Specified	N	MGI:61266
MGI:3811900	F	MP:0002636	delayed vaginal opening	Pubt1<C57BL/6J>/Pubt1<C57BL/6J>	involves: C3H/HeJ * C57BL/6J	N	18725948
MGI:3811901	F	MP:0002636	delayed vaginal opening	Pubt1<C3H/HeJ>/Pubt1<C57BL/6J>	involves: C3H/HeJ * C57BL/6J	N	18725948
MGI:3812133	M	MP:0002435	abnormal effector T cell morphology	Dsg4<hage>/Dsg4<hage>,Fas<lpr>/Fas<lpr>,X/Yaa	EOD-Dsg4<hage>	N	18677469
MGI:3812133	M	MP:0001219	thick epidermis	Dsg4<hage>/Dsg4<hage>,Fas<lpr>/Fas<lpr>,X/Yaa	EOD-Dsg4<hage>	N	18677469
MGI:3812133	M	MP:0001661	extended life span	Dsg4<hage>/Dsg4<hage>,Fas<lpr>/Fas<lpr>,X/Yaa	EOD-Dsg4<hage>	N	18677469
MGI:3812133	M	MP:0000383	abnormal hair follicle orientation	Dsg4<hage>/Dsg4<hage>,Fas<lpr>/Fas<lpr>,X/Yaa	EOD-Dsg4<hage>	N	18677469
MGI:3812133	M	MP:0000377	abnormal hair follicle morphology	Dsg4<hage>/Dsg4<hage>,Fas<lpr>/Fas<lpr>,X/Yaa	EOD-Dsg4<hage>	N	18677469
MGI:3812133	M	MP:0001265	decreased body size	Dsg4<hage>/Dsg4<hage>,Fas<lpr>/Fas<lpr>,X/Yaa	EOD-Dsg4<hage>	N	18677469
MGI:3812133	M	MP:0000359	abnormal mast cell morphology	Dsg4<hage>/Dsg4<hage>,Fas<lpr>/Fas<lpr>,X/Yaa	EOD-Dsg4<hage>	N	18677469
MGI:3812133	M	MP:0001284	absent vibrissae	Dsg4<hage>/Dsg4<hage>,Fas<lpr>/Fas<lpr>,X/Yaa	EOD-Dsg4<hage>	N	18677469
MGI:3812133	M	MP:0000416	sparse hair	Dsg4<hage>/Dsg4<hage>,Fas<lpr>/Fas<lpr>,X/Yaa	EOD-Dsg4<hage>	N	18677469
MGI:3812187	F	MP:0001926	female infertility	Ooep<Gt(139A2)Cmhd>/Ooep<Gt(139A2)Cmhd>	involves: 129S1/Sv * 129X1/SvJ	N	18804437
MGI:3812188	F	MP:0001926	female infertility	Nlrp5<tm1Zbt>/Nlrp5<tm1Zbt>,Ooep<Gt(139A2)Cmhd>/Ooep<Gt(139A2)Cmhd>	involves: 129S1/Sv * 129X1/SvJ	N	18804437
MGI:3812319	M	MP:0003725	increased autoantibody level	Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812319	M	MP:0001873	stomach inflammation	Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0001870	salivary gland inflammation	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0000274	enlarged heart	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0002490	abnormal immunoglobulin level	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0001873	stomach inflammation	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0000598	abnormal liver morphology	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0003725	increased autoantibody level	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0008566	increased interferon-gamma secretion	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0008687	increased interleukin-2 secretion	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0008699	increased interleukin-4 secretion	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0000693	spleen hyperplasia	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0001846	increased inflammatory response	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0008102	lymph node hyperplasia	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0001861	lung inflammation	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0001856	myocarditis	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0002493	increased IgG level	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0004946	abnormal regulatory T cell physiology	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0004973	increased regulatory T cell number	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0002497	increased IgE level	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0002083	premature death	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812320	M	MP:0008826	abnormal splenic cell ratio	Ctla4<tm1Saka>/Ctla4<tm1Saka>,Foxp3<tm1(cre)Saka>/Y	involves: BALB/c	N	18845758
MGI:3812359	F	MP:0012008	delayed parturition	Ptgs1<tm1Unc>/Ptgs1<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6 * CD-1	N	10944235
MGI:3812385	F	MP:0012008	delayed parturition	Ptgs1<tm1Unc>/Ptgs1<+>,Ptgs2<tm1Unc>/Ptgs2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	11158594
MGI:3812386	F	MP:0012008	delayed parturition	Ptgs1<tm1Unc>/Ptgs1<tm1Unc>,Ptgs2<tm1Unc>/Ptgs2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	11158594
MGI:3812454	F	MP:0005166	decreased susceptibility to injury	Adora2b<tm1Dgen>/Adora2b<tm1Dgen>	involves: 129P2/OlaHsd	N	25538227
MGI:3812457	M	MP:0001379	abnormal penile erection	Adora2b<tm1Dgen>/Adora2b<tm1Dgen>	B6.129P2-Adora2b<tm1Dgen>	N	18340377
MGI:3812462	F	MP:0001140	abnormal vagina epithelium morphology	Krt14<tm1Efu>/Krt14<tm1Efu>	involves: 129	N	7539810
MGI:3812468	M	MP:0001379	abnormal penile erection	Hba<tm1Paz>/Hba<tm1Paz>,Hbb<tm1Tow>/Hbb<tm1Tow>,Tg(HBA-HBBs)41Paz/0	involves: 129 * Black Swiss * C57BL/6 * DBA/2 * FVB/N	N	18340377
MGI:3812468	M	MP:0003415	priapism	Hba<tm1Paz>/Hba<tm1Paz>,Hbb<tm1Tow>/Hbb<tm1Tow>,Tg(HBA-HBBs)41Paz/0	involves: 129 * Black Swiss * C57BL/6 * DBA/2 * FVB/N	N	18340377
MGI:3812473	F	MP:0003231	abnormal placenta vasculature	Ada<tm1Mw>/Ada<tm1Mw>	involves: 129S7/SvEvBrd	N	25538227
MGI:3812473	F	MP:0001711	abnormal placenta morphology	Ada<tm1Mw>/Ada<tm1Mw>	involves: 129S7/SvEvBrd	N	25538227
MGI:3812473	F	MP:0004921	decreased placenta weight	Ada<tm1Mw>/Ada<tm1Mw>	involves: 129S7/SvEvBrd	N	25538227
MGI:3812473	F	MP:0004259	small placenta	Ada<tm1Mw>/Ada<tm1Mw>	involves: 129S7/SvEvBrd	N	25538227
MGI:3813259	F	MP:0001926	female infertility	Lepr<db-2J>/Lepr<db-2J>	involves: C57BL/6J * STOCK Tyrp1<b> Whrn<wi>	N	378276
MGI:3813259	F	MP:0001143	constricted vagina orifice	Lepr<db-2J>/Lepr<db-2J>	involves: C57BL/6J * STOCK Tyrp1<b> Whrn<wi>	N	378276
MGI:3813259	M	MP:0001380	reduced male mating frequency	Lepr<db-2J>/Lepr<db-2J>	involves: C57BL/6J * STOCK Tyrp1<b> Whrn<wi>	N	378276
MGI:3813259	F	MP:0009019	abnormal metestrus	Lepr<db-2J>/Lepr<db-2J>	involves: C57BL/6J * STOCK Tyrp1<b> Whrn<wi>	N	378276
MGI:3813259	F	MP:0002637	small uterus	Lepr<db-2J>/Lepr<db-2J>	involves: C57BL/6J * STOCK Tyrp1<b> Whrn<wi>	N	378276
MGI:3813259	F	MP:0009010	abnormal diestrus	Lepr<db-2J>/Lepr<db-2J>	involves: C57BL/6J * STOCK Tyrp1<b> Whrn<wi>	N	378276
MGI:3813259	M	MP:0002716	small male preputial gland	Lepr<db-2J>/Lepr<db-2J>	involves: C57BL/6J * STOCK Tyrp1<b> Whrn<wi>	N	378276
MGI:3813269	M	MP:0001925	male infertility	Lepr<db-NCSU>/Lepr<db-NCSU>	involves: CD-1	N	10666131
MGI:3813269	F	MP:0001926	female infertility	Lepr<db-NCSU>/Lepr<db-NCSU>	involves: CD-1	N	10666131
MGI:3813305	M	MP:0004901	decreased male germ cell number	Nphp1<tm1.1Hung>/Nphp1<tm1.1Hung>	B6.Cg-Nphp1<tm1.1Hung>	N	18684731
MGI:3813305	M	MP:0002687	oligozoospermia	Nphp1<tm1.1Hung>/Nphp1<tm1.1Hung>	B6.Cg-Nphp1<tm1.1Hung>	N	18684731
MGI:3813305	M	MP:0001925	male infertility	Nphp1<tm1.1Hung>/Nphp1<tm1.1Hung>	B6.Cg-Nphp1<tm1.1Hung>	N	18684731
MGI:3813305	M	MP:0004182	abnormal spermiation	Nphp1<tm1.1Hung>/Nphp1<tm1.1Hung>	B6.Cg-Nphp1<tm1.1Hung>	N	18684731
MGI:3813305	M	MP:0008892	abnormal sperm flagellum morphology	Nphp1<tm1.1Hung>/Nphp1<tm1.1Hung>	B6.Cg-Nphp1<tm1.1Hung>	N	18684731
MGI:3813305	M	MP:0004852	decreased testis weight	Nphp1<tm1.1Hung>/Nphp1<tm1.1Hung>	B6.Cg-Nphp1<tm1.1Hung>	N	18684731
MGI:3813305	M	MP:0005578	teratozoospermia	Nphp1<tm1.1Hung>/Nphp1<tm1.1Hung>	B6.Cg-Nphp1<tm1.1Hung>	N	18684731
MGI:3813455	F	MP:0011727	ectopic ovary	Foxc1<ch>/Foxc1<+>	involves: CBA * STOCK Tyr<c> f	N	5500588
MGI:3813455	M	MP:0011410	ectopic testis	Foxc1<ch>/Foxc1<+>	involves: CBA * STOCK Tyr<c> f	N	5500588
MGI:3813525	F	MP:0006078	abnormal nipple morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(KRT14-cre)#Smr/0	involves: 129S4/SvJae * C57BL/6J * SJL/J	N	18757421
MGI:3813538	M	MP:0009592	increased Leydig cell tumor incidence	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	N	17044021
MGI:3813538	M	MP:0001152	increased Leydig cell number	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	N	17044021
MGI:3813538	F	MP:0008000	increased ovary tumor incidence	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	N	17044021
MGI:3813539	M	MP:0009592	increased Leydig cell tumor incidence	Men1<tm2.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	N	17044021
MGI:3813539	F	MP:0008000	increased ovary tumor incidence	Men1<tm2.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	N	17044021
MGI:3813587	F	MP:0001128	ovary hyperplasia	Kit<tm1.1Bsm>/Kit<tm1.1Bsm>	involves: 129S1/Sv * BALB/c * C57BL/6J * FVB/N	N	10716931
MGI:3813587	M	MP:0001155	arrest of spermatogenesis	Kit<tm1.1Bsm>/Kit<tm1.1Bsm>	involves: 129S1/Sv * BALB/c * C57BL/6J * FVB/N	N	10716931
MGI:3813587	F	MP:0001129	impaired ovarian folliculogenesis	Kit<tm1.1Bsm>/Kit<tm1.1Bsm>	involves: 129S1/Sv * BALB/c * C57BL/6J * FVB/N	N	10716931
MGI:3813587	F	MP:0002016	ovary cyst	Kit<tm1.1Bsm>/Kit<tm1.1Bsm>	involves: 129S1/Sv * BALB/c * C57BL/6J * FVB/N	N	10716931
MGI:3813587	F	MP:0031381	decreased secondary ovarian follicle number	Kit<tm1.1Bsm>/Kit<tm1.1Bsm>	involves: 129S1/Sv * BALB/c * C57BL/6J * FVB/N	N	10716931
MGI:3813587	M	MP:0001152	increased Leydig cell number	Kit<tm1.1Bsm>/Kit<tm1.1Bsm>	involves: 129S1/Sv * BALB/c * C57BL/6J * FVB/N	N	10716931
MGI:3813587	F	MP:0011129	decreased tertiary ovarian follicle number	Kit<tm1.1Bsm>/Kit<tm1.1Bsm>	involves: 129S1/Sv * BALB/c * C57BL/6J * FVB/N	N	10716931
MGI:3813587	M	MP:0001925	male infertility	Kit<tm1.1Bsm>/Kit<tm1.1Bsm>	involves: 129S1/Sv * BALB/c * C57BL/6J * FVB/N	N	10716931
MGI:3813587	F	MP:0001126	abnormal ovary morphology	Kit<tm1.1Bsm>/Kit<tm1.1Bsm>	involves: 129S1/Sv * BALB/c * C57BL/6J * FVB/N	N	10716931
MGI:3813587	M	MP:0004901	decreased male germ cell number	Kit<tm1.1Bsm>/Kit<tm1.1Bsm>	involves: 129S1/Sv * BALB/c * C57BL/6J * FVB/N	N	10716931
MGI:3813587	F	MP:0001923	reduced female fertility	Kit<tm1.1Bsm>/Kit<tm1.1Bsm>	involves: 129S1/Sv * BALB/c * C57BL/6J * FVB/N	N	10716931
MGI:3813633	F	MP:0009092	endometrium hyperplasia	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	18632614
MGI:3813633	F	MP:0004868	increased endometrial carcinoma incidence	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	18632614
MGI:3813634	F	MP:0004906	enlarged uterus	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129 * C57BL/6	N	18632614
MGI:3813634	F	MP:0009092	endometrium hyperplasia	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129 * C57BL/6	N	18632614
MGI:3813634	F	MP:0004868	increased endometrial carcinoma incidence	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129 * C57BL/6	N	18632614
MGI:3813670	M	MP:0001147	small testis	Kit<W-35J>/Kit<+>	C57BL/6J-Kit<W-35J>/J	N	7274658
MGI:3813675	M	MP:0001147	small testis	Kit<W-38J>/Kit<+>	involves: C57BL/6J	N	7274658
MGI:3813676	F	MP:0001127	small ovary	Kit<W-39J>/Kit<W-39J>	C57BL/6J-Kit<W-39J>/J	N	7274658
MGI:3813676	M	MP:0001147	small testis	Kit<W-39J>/Kit<W-39J>	C57BL/6J-Kit<W-39J>/J	N	7274658
MGI:3813676	F	MP:0008871	abnormal ovarian follicle number	Kit<W-39J>/Kit<W-39J>	C57BL/6J-Kit<W-39J>/J	N	7274658
MGI:3813679	M	MP:0001147	small testis	Kit<W-40J>/Kit<+>	C57BL/6J-Kit<W-40J>/J	N	7274658
MGI:3813680	F	MP:0008871	abnormal ovarian follicle number	Kit<W-41J>/Kit<W-41J>	C57BL/6J-Kit<W-41J>/J	N	7274658
MGI:3813680	F	MP:0001127	small ovary	Kit<W-41J>/Kit<W-41J>	C57BL/6J-Kit<W-41J>/J	N	7274658
MGI:3813683	M	MP:0001147	small testis	Kit<W-43J>/Kit<+>	C57BL/6J-Kit<W-43J>/J	N	7274658
MGI:3813684	F	MP:0008871	abnormal ovarian follicle number	Kit<W-39J>/Kit<W-41J>	involves: C57BL/6J	N	7274658
MGI:3813684	F	MP:0001127	small ovary	Kit<W-39J>/Kit<W-41J>	involves: C57BL/6J	N	7274658
MGI:3813685	F	MP:0001127	small ovary	Kit<W-41J>/Kit<W-44J>	involves: C3H/HeJ * C57BL/6J	N	7274658
MGI:3813685	F	MP:0008871	abnormal ovarian follicle number	Kit<W-41J>/Kit<W-44J>	involves: C3H/HeJ * C57BL/6J	N	7274658
MGI:3813686	M	MP:0001147	small testis	Kit<W-39J>/Kit<W-v>	involves: C57BL * C57BL/6J	N	7274658
MGI:3813686	F	MP:0008871	abnormal ovarian follicle number	Kit<W-39J>/Kit<W-v>	involves: C57BL * C57BL/6J	N	7274658
MGI:3813686	F	MP:0001127	small ovary	Kit<W-39J>/Kit<W-v>	involves: C57BL * C57BL/6J	N	7274658
MGI:3813687	F	MP:0001127	small ovary	Kit<W-39J>/Kit<W-44J>	involves: C3H/HeJ * C57BL/6J	N	7274658
MGI:3813687	F	MP:0008871	abnormal ovarian follicle number	Kit<W-39J>/Kit<W-44J>	involves: C3H/HeJ * C57BL/6J	N	7274658
MGI:3813687	F	MP:0001923	reduced female fertility	Kit<W-39J>/Kit<W-44J>	involves: C3H/HeJ * C57BL/6J	N	7274658
MGI:3813687	M	MP:0001147	small testis	Kit<W-39J>/Kit<W-44J>	involves: C3H/HeJ * C57BL/6J	N	7274658
MGI:3813687	M	MP:0001925	male infertility	Kit<W-39J>/Kit<W-44J>	involves: C3H/HeJ * C57BL/6J	N	7274658
MGI:3813688	F	MP:0001127	small ovary	Kit<W-39J>/Kit<W-40J>	involves: C57BL/6J	N	7274658
MGI:3813688	M	MP:0001147	small testis	Kit<W-39J>/Kit<W-40J>	involves: C57BL/6J	N	7274658
MGI:3813688	F	MP:0008871	abnormal ovarian follicle number	Kit<W-39J>/Kit<W-40J>	involves: C57BL/6J	N	7274658
MGI:3813688	M	MP:0001156	abnormal spermatogenesis	Kit<W-39J>/Kit<W-40J>	involves: C57BL/6J	N	7274658
MGI:3813689	F	MP:0001127	small ovary	Kit<W-37J>/Kit<W-39J>	involves: C57BL/6J	N	7274658
MGI:3813689	F	MP:0008871	abnormal ovarian follicle number	Kit<W-37J>/Kit<W-39J>	involves: C57BL/6J	N	7274658
MGI:3813689	M	MP:0001147	small testis	Kit<W-37J>/Kit<W-39J>	involves: C57BL/6J	N	7274658
MGI:3813689	M	MP:0001156	abnormal spermatogenesis	Kit<W-37J>/Kit<W-39J>	involves: C57BL/6J	N	7274658
MGI:3813691	M	MP:0001156	abnormal spermatogenesis	Kit<W-38J>/Kit<W-39J>	involves: C57BL/6J	N	7274658
MGI:3813691	F	MP:0001127	small ovary	Kit<W-38J>/Kit<W-39J>	involves: C57BL/6J	N	7274658
MGI:3813691	M	MP:0001147	small testis	Kit<W-38J>/Kit<W-39J>	involves: C57BL/6J	N	7274658
MGI:3813691	F	MP:0008871	abnormal ovarian follicle number	Kit<W-38J>/Kit<W-39J>	involves: C57BL/6J	N	7274658
MGI:3813692	M	MP:0001147	small testis	Kit<W-34J>/Kit<W-39J>	involves: C57BL/6J	N	7274658
MGI:3813692	M	MP:0001156	abnormal spermatogenesis	Kit<W-34J>/Kit<W-39J>	involves: C57BL/6J	N	7274658
MGI:3813692	F	MP:0001127	small ovary	Kit<W-34J>/Kit<W-39J>	involves: C57BL/6J	N	7274658
MGI:3813692	F	MP:0008871	abnormal ovarian follicle number	Kit<W-34J>/Kit<W-39J>	involves: C57BL/6J	N	7274658
MGI:3813693	F	MP:0001127	small ovary	Kit<W-39J>/Kit<W-42J>	involves: C57BL/6J	N	7274658
MGI:3813693	M	MP:0001156	abnormal spermatogenesis	Kit<W-39J>/Kit<W-42J>	involves: C57BL/6J	N	7274658
MGI:3813693	F	MP:0008871	abnormal ovarian follicle number	Kit<W-39J>/Kit<W-42J>	involves: C57BL/6J	N	7274658
MGI:3813693	M	MP:0001147	small testis	Kit<W-39J>/Kit<W-42J>	involves: C57BL/6J	N	7274658
MGI:3813694	F	MP:0001127	small ovary	Kit<W-39J>/Kit<W>	involves: C57BL/6J	N	7274658
MGI:3813694	M	MP:0001156	abnormal spermatogenesis	Kit<W-39J>/Kit<W>	involves: C57BL/6J	N	7274658
MGI:3813694	M	MP:0001147	small testis	Kit<W-39J>/Kit<W>	involves: C57BL/6J	N	7274658
MGI:3813694	F	MP:0008871	abnormal ovarian follicle number	Kit<W-39J>/Kit<W>	involves: C57BL/6J	N	7274658
MGI:3813695	M	MP:0001156	abnormal spermatogenesis	Kit<W-39J>/Kit<W-43J>	involves: C57BL/6J	N	7274658
MGI:3813695	M	MP:0001147	small testis	Kit<W-39J>/Kit<W-43J>	involves: C57BL/6J	N	7274658
MGI:3813695	F	MP:0001127	small ovary	Kit<W-39J>/Kit<W-43J>	involves: C57BL/6J	N	7274658
MGI:3813695	F	MP:0008871	abnormal ovarian follicle number	Kit<W-39J>/Kit<W-43J>	involves: C57BL/6J	N	7274658
MGI:3813701	M	MP:0004852	decreased testis weight	Pum2<Gt(XE772)Byg>/Pum2<Gt(XE772)Byg>	B6.129P2-Pum2<Gt(XE772)Byg>	N	17219433
MGI:3813701	M	MP:0001154	seminiferous tubule degeneration	Pum2<Gt(XE772)Byg>/Pum2<Gt(XE772)Byg>	B6.129P2-Pum2<Gt(XE772)Byg>	N	17219433
MGI:3813702	M	MP:0004852	decreased testis weight	Dazl<tm1Hjc>/Dazl<+>,Pum2<Gt(XE772)Byg>/Pum2<Gt(XE772)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	17219433
MGI:3813724	F	MP:0000628	abnormal mammary gland development	Tbx3<tm1.1(cre)Vmc>/Tbx3<tm1.1(cre)Vmc>	involves: 129P2/OlaHsd * FVB	N	17473172
MGI:3813810	M	MP:0001156	abnormal spermatogenesis	Kit<W-j>/Kit<W-j>	involves: C3H	N	MGI:51911
MGI:3813827	M	MP:0001150	enlarged scrotum	Rgsc1085/Rgsc1085<+>	involves: C57BL/6JJcl * DBA/2JJcl	N	MGI:3778963
MGI:3813923	F	MP:0001883	increased mammary adenocarcinoma incidence	Stat1<tm1Dlv>/Stat1<tm1Dlv>	B6.129S-Stat1<tm1Dlv>	N	22264274
MGI:3813939	M	MP:0002420	abnormal adaptive immunity	Il2rg<tm1Wjl>/Y,Rag1<tm1Mom>/Rag1<tm1Mom>	NOD.Cg-Rag1<tm1Mom> Il2rg<tm1Wjl>/SzJ	N	18785974
MGI:3813939	M	MP:0014263	decreased spleen B cell follicle number	Il2rg<tm1Wjl>/Y,Rag1<tm1Mom>/Rag1<tm1Mom>	NOD.Cg-Rag1<tm1Mom> Il2rg<tm1Wjl>/SzJ	N	18785974
MGI:3813939	M	MP:0010250	absent thymus cortex	Il2rg<tm1Wjl>/Y,Rag1<tm1Mom>/Rag1<tm1Mom>	NOD.Cg-Rag1<tm1Mom> Il2rg<tm1Wjl>/SzJ	N	18785974
MGI:3813939	M	MP:0003884	decreased macrophage cell number	Il2rg<tm1Wjl>/Y,Rag1<tm1Mom>/Rag1<tm1Mom>	NOD.Cg-Rag1<tm1Mom> Il2rg<tm1Wjl>/SzJ	N	18785974
MGI:3813939	M	MP:0014130	thymus cyst	Il2rg<tm1Wjl>/Y,Rag1<tm1Mom>/Rag1<tm1Mom>	NOD.Cg-Rag1<tm1Mom> Il2rg<tm1Wjl>/SzJ	N	18785974
MGI:3813939	M	MP:0013587	absent thymus medulla	Il2rg<tm1Wjl>/Y,Rag1<tm1Mom>/Rag1<tm1Mom>	NOD.Cg-Rag1<tm1Mom> Il2rg<tm1Wjl>/SzJ	N	18785974
MGI:3813939	M	MP:0000689	abnormal spleen morphology	Il2rg<tm1Wjl>/Y,Rag1<tm1Mom>/Rag1<tm1Mom>	NOD.Cg-Rag1<tm1Mom> Il2rg<tm1Wjl>/SzJ	N	18785974
MGI:3813939	M	MP:0008041	absent NK T cells	Il2rg<tm1Wjl>/Y,Rag1<tm1Mom>/Rag1<tm1Mom>	NOD.Cg-Rag1<tm1Mom> Il2rg<tm1Wjl>/SzJ	N	18785974
MGI:3813939	M	MP:0002419	abnormal innate immunity	Il2rg<tm1Wjl>/Y,Rag1<tm1Mom>/Rag1<tm1Mom>	NOD.Cg-Rag1<tm1Mom> Il2rg<tm1Wjl>/SzJ	N	18785974
MGI:3813939	M	MP:0005671	abnormal response to transplant	Il2rg<tm1Wjl>/Y,Rag1<tm1Mom>/Rag1<tm1Mom>	NOD.Cg-Rag1<tm1Mom> Il2rg<tm1Wjl>/SzJ	N	18785974
MGI:3813939	M	MP:0000703	abnormal thymus morphology	Il2rg<tm1Wjl>/Y,Rag1<tm1Mom>/Rag1<tm1Mom>	NOD.Cg-Rag1<tm1Mom> Il2rg<tm1Wjl>/SzJ	N	18785974
MGI:3813941	F	MP:0005386	behavior/neurological phenotype	Apln<tm1Pngr>/Apln<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6	Y	17673668
MGI:3813941	F	MP:0005378	growth/size/body region phenotype	Apln<tm1Pngr>/Apln<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6	Y	17673668
MGI:3813941	F	MP:0005385	cardiovascular system phenotype	Apln<tm1Pngr>/Apln<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6	Y	17673668
MGI:3813941	F	MP:0031633	decreased heart left ventricle muscle contractility	Apln<tm1Pngr>/Apln<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6	N	17673668
MGI:3813943	M	MP:0005385	cardiovascular system phenotype	Apln<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	Y	17673668
MGI:3813943	M	MP:0004485	increased response of heart to induced stress	Apln<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17673668
MGI:3813943	M	MP:0005386	behavior/neurological phenotype	Apln<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	Y	17673668
MGI:3813943	M	MP:0005378	growth/size/body region phenotype	Apln<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	Y	17673668
MGI:3813943	M	MP:0031633	decreased heart left ventricle muscle contractility	Apln<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6	N	17673668
MGI:3814055	M	MP:0003950	abnormal plasma membrane morphology	Piga<tm2Tak>/Y	chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	8611683
MGI:3814055	M	MP:0011091	prenatal lethality, complete penetrance	Piga<tm2Tak>/Y	chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	8611683
MGI:3814173	M	MP:0005159	azoospermia	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	F	MP:0001131	abnormal ovarian follicle morphology	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	M	MP:0001146	abnormal testis morphology	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	F	MP:0001125	abnormal oocyte morphology	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	M	MP:0001925	male infertility	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	F	MP:0001132	absent mature ovarian follicles	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	F	MP:0001129	impaired ovarian folliculogenesis	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	M	MP:0004852	decreased testis weight	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	M	MP:0002784	abnormal Sertoli cell morphology	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	F	MP:0009368	absent theca folliculi	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	F	MP:0003696	abnormal zona pellucida morphology	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	F	MP:0003697	absent zona pellucida	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	M	MP:0004884	abnormal testis physiology	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	F	MP:0008868	abnormal granulosa cell morphology	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	M	MP:0008279	arrest of spermiogenesis	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814173	F	MP:0001926	female infertility	Fads2<tm1Wst>/Fads2<tm1Wst>	involves: 129P2/OlaHsd	N	19172737
MGI:3814175	F	MP:0003675	kidney cyst	Pkhd1<tm1Cjwa>/Pkhd1<tm1Cjwa>	involves: 129S6/SvEvTac * FVB/N	N	17519956
MGI:3814175	F	MP:0009050	dilated proximal convoluted tubule	Pkhd1<tm1Cjwa>/Pkhd1<tm1Cjwa>	involves: 129S6/SvEvTac * FVB/N	N	17519956
MGI:3814175	F	MP:0011352	proximal convoluted tubule brush border loss	Pkhd1<tm1Cjwa>/Pkhd1<tm1Cjwa>	involves: 129S6/SvEvTac * FVB/N	N	17519956
MGI:3814198	F	MP:0002640	reticulocytosis	Piga<tm1Bsl>/Piga<+>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S1/Sv * FVB/NJ	N	10556176
MGI:3814198	F	MP:0001436	abnormal suckling behavior	Piga<tm1Bsl>/Piga<+>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S1/Sv * FVB/NJ	N	10377440
MGI:3814198	F	MP:0002123	abnormal definitive hematopoiesis	Piga<tm1Bsl>/Piga<+>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S1/Sv * FVB/NJ	N	10556176
MGI:3814198	F	MP:0002447	abnormal erythrocyte morphology	Piga<tm1Bsl>/Piga<+>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S1/Sv * FVB/NJ	N	10556176
MGI:3814198	F	MP:0003743	abnormal facial morphology	Piga<tm1Bsl>/Piga<+>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S1/Sv * FVB/NJ	N	10377440
MGI:3814198	F	MP:0011090	perinatal lethality, incomplete penetrance	Piga<tm1Bsl>/Piga<+>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S1/Sv * FVB/NJ	N	10556176
MGI:3814198	F	MP:0031085	increased erythrocyte osmotic fragility	Piga<tm1Bsl>/Piga<+>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S1/Sv * FVB/NJ	N	10556176
MGI:3814198	F	MP:0000111	cleft palate	Piga<tm1Bsl>/Piga<+>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S1/Sv * FVB/NJ	N	10377440
MGI:3814198	F	MP:0003656	abnormal erythrocyte physiology	Piga<tm1Bsl>/Piga<+>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S1/Sv * FVB/NJ	N	10556176
MGI:3814205	F	MP:0002947	increased hemangioma incidence	Piga<tm1Bsl>/Piga<+>,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * C57BL/6 * CBA/Ca	N	11535627
MGI:3814205	F	MP:0001402	decreased locomotor activity	Piga<tm1Bsl>/Piga<+>,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * C57BL/6 * CBA/Ca	N	11535627
MGI:3814205	F	MP:0000746	weakness	Piga<tm1Bsl>/Piga<+>,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * C57BL/6 * CBA/Ca	N	11535627
MGI:3814205	F	MP:0001263	weight loss	Piga<tm1Bsl>/Piga<+>,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * C57BL/6 * CBA/Ca	N	11535627
MGI:3814205	F	MP:0002023	increased B cell derived lymphoma incidence	Piga<tm1Bsl>/Piga<+>,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * C57BL/6 * CBA/Ca	N	11535627
MGI:3814206	M	MP:0002023	increased B cell derived lymphoma incidence	Piga<tm1Bsl>/Y,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * C57BL/6 * CBA/Ca	N	11535627
MGI:3814206	M	MP:0002947	increased hemangioma incidence	Piga<tm1Bsl>/Y,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * C57BL/6 * CBA/Ca	N	11535627
MGI:3814206	M	MP:0001263	weight loss	Piga<tm1Bsl>/Y,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * C57BL/6 * CBA/Ca	N	11535627
MGI:3814206	M	MP:0000746	weakness	Piga<tm1Bsl>/Y,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * C57BL/6 * CBA/Ca	N	11535627
MGI:3814206	M	MP:0001402	decreased locomotor activity	Piga<tm1Bsl>/Y,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * C57BL/6 * CBA/Ca	N	11535627
MGI:3814206	M	MP:0001406	abnormal gait	Piga<tm1Bsl>/Y,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * C57BL/6 * CBA/Ca	N	11535627
MGI:3814213	M	MP:0001261	obese	Pomc<tm1Low>/Pomc<tm1Low>	B6.129S2-Pomc<tm1Low>	N	12697680
MGI:3814213	M	MP:0006094	increased fat cell size	Pomc<tm1Low>/Pomc<tm1Low>	B6.129S2-Pomc<tm1Low>	N	12697680
MGI:3814213	M	MP:0009302	increased renal fat pad weight	Pomc<tm1Low>/Pomc<tm1Low>	B6.129S2-Pomc<tm1Low>	N	12697680
MGI:3814213	M	MP:0005376	homeostasis/metabolism phenotype	Pomc<tm1Low>/Pomc<tm1Low>	B6.129S2-Pomc<tm1Low>	Y	12697680
MGI:3814213	M	MP:0009304	increased retroperitoneal fat pad weight	Pomc<tm1Low>/Pomc<tm1Low>	B6.129S2-Pomc<tm1Low>	N	12697680
MGI:3814213	M	MP:0002079	increased circulating insulin level	Pomc<tm1Low>/Pomc<tm1Low>	B6.129S2-Pomc<tm1Low>	N	12697680
MGI:3814213	M	MP:0005293	impaired glucose tolerance	Pomc<tm1Low>/Pomc<tm1Low>	B6.129S2-Pomc<tm1Low>	N	12697680
MGI:3814213	M	MP:0005669	increased circulating leptin level	Pomc<tm1Low>/Pomc<tm1Low>	B6.129S2-Pomc<tm1Low>	N	12697680
MGI:3814213	M	MP:0009292	increased inguinal fat pad weight	Pomc<tm1Low>/Pomc<tm1Low>	B6.129S2-Pomc<tm1Low>	N	12697680
MGI:3814213	M	MP:0010024	increased total body fat amount	Pomc<tm1Low>/Pomc<tm1Low>	B6.129S2-Pomc<tm1Low>	N	12697680
MGI:3814213	M	MP:0009285	increased gonadal fat pad weight	Pomc<tm1Low>/Pomc<tm1Low>	B6.129S2-Pomc<tm1Low>	N	12697680
MGI:3814213	M	MP:0001433	polyphagia	Pomc<tm1Low>/Pomc<tm1Low>	B6.129S2-Pomc<tm1Low>	N	12697680
MGI:3814225	M	MP:0009114	decreased pancreatic beta cell mass	Ildr2<Dbsm1-DBA/2J>/Ildr2<Dbsm1-DBA/2J>,Lep<ob>/Lep<ob>	B6.Cg-Ildr2<Dbsm1-DBA/2J> Lep<ob>	N	18654634
MGI:3814225	M	MP:0001559	hyperglycemia	Ildr2<Dbsm1-DBA/2J>/Ildr2<Dbsm1-DBA/2J>,Lep<ob>/Lep<ob>	B6.Cg-Ildr2<Dbsm1-DBA/2J> Lep<ob>	N	18654634
MGI:3814225	M	MP:0005293	impaired glucose tolerance	Ildr2<Dbsm1-DBA/2J>/Ildr2<Dbsm1-DBA/2J>,Lep<ob>/Lep<ob>	B6.Cg-Ildr2<Dbsm1-DBA/2J> Lep<ob>	N	18654634
MGI:3814225	M	MP:0002727	decreased circulating insulin level	Ildr2<Dbsm1-DBA/2J>/Ildr2<Dbsm1-DBA/2J>,Lep<ob>/Lep<ob>	B6.Cg-Ildr2<Dbsm1-DBA/2J> Lep<ob>	N	18654634
MGI:3814236	F	MP:0010768	mortality/aging	Ar<tm4(AR)Dmr>/Ar<+>	involves: 129S1/Sv * C57BL/6J	Y	16981011
MGI:3814236	F	MP:0002781	increased circulating testosterone level	Ar<tm4(AR)Dmr>/Ar<+>	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3814236	F	MP:0011533	increased urine major urinary protein level	Ar<tm4(AR)Dmr>/Ar<+>	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3814236	F	MP:0005378	growth/size/body region phenotype	Ar<tm4(AR)Dmr>/Ar<+>	involves: 129S1/Sv * C57BL/6J	Y	16981011
MGI:3814236	F	MP:0000747	muscle weakness	Ar<tm4(AR)Dmr>/Ar<+>	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3814236	F	MP:0010053	decreased grip strength	Ar<tm4(AR)Dmr>/Ar<+>	involves: 129S1/Sv * C57BL/6J	N	16981011
MGI:3814365	F	MP:0010299	increased mammary gland tumor incidence	Brca2<tm1Mbn>/Brca2<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814365	F	MP:0009078	adrenal gland hyperplasia	Brca2<tm1Mbn>/Brca2<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814367	F	MP:0001130	abnormal ovarian folliculogenesis	Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814367	F	MP:0009733	absent nipple	Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814367	F	MP:0004833	ovary atrophy	Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814367	M	MP:0000628	abnormal mammary gland development	Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814367	F	MP:0004894	uterus atrophy	Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814367	F	MP:0001132	absent mature ovarian follicles	Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814367	F	MP:0001134	absent corpus luteum	Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814367	F	MP:0001131	abnormal ovarian follicle morphology	Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814367	F	MP:0001140	abnormal vagina epithelium morphology	Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814370	F	MP:0004894	uterus atrophy	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814370	F	MP:0001132	absent mature ovarian follicles	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814370	F	MP:0001140	abnormal vagina epithelium morphology	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814370	F	MP:0009733	absent nipple	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814370	F	MP:0001131	abnormal ovarian follicle morphology	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814370	F	MP:0009078	adrenal gland hyperplasia	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814370	F	MP:0001134	absent corpus luteum	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814370	F	MP:0001130	abnormal ovarian folliculogenesis	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814370	M	MP:0000628	abnormal mammary gland development	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814370	F	MP:0004833	ovary atrophy	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	N	11215675
MGI:3814450	M	MP:0008261	arrest of male meiosis	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129 * C57BL/6	N	18694567
MGI:3814451	M	MP:0005169	abnormal male meiosis	Mael<tm1Bort>/Mael<tm1Bort>,Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129 * C57BL/6	N	18694567
MGI:3814452	M	MP:0001925	male infertility	Mael<tm1Bort>/Mael<tm1Bort>	B6.129S4-Mael<tm1Bort>	N	18694567
MGI:3814452	M	MP:0006379	abnormal spermatocyte morphology	Mael<tm1Bort>/Mael<tm1Bort>	B6.129S4-Mael<tm1Bort>	N	18694567
MGI:3814452	M	MP:0001147	small testis	Mael<tm1Bort>/Mael<tm1Bort>	B6.129S4-Mael<tm1Bort>	N	18694567
MGI:3814452	M	MP:0014052	increased male germ cell apoptosis	Mael<tm1Bort>/Mael<tm1Bort>	B6.129S4-Mael<tm1Bort>	N	18694567
MGI:3814452	M	MP:0005169	abnormal male meiosis	Mael<tm1Bort>/Mael<tm1Bort>	B6.129S4-Mael<tm1Bort>	N	18694567
MGI:3814537	M	MP:0004852	decreased testis weight	Tg(Trp53A135V)L3Ber/0	involves: C57BL/6 * CD-1	N	11780111
MGI:3814539	M	MP:0001940	testis hypoplasia	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11780111
MGI:3814539	M	MP:0004852	decreased testis weight	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	N	11780111
MGI:3814544	F	MP:0000628	abnormal mammary gland development	Trp53<tm1Ldo>/Trp53<+>	B6.129S7-Trp53<tm1Ldo>	N	17996864
MGI:3814723	M	MP:0001925	male infertility	Trl/Trl<+>	C3FeLe.B6-a Trl/J	N	MGI:3814697
MGI:3814725	M	MP:0001156	abnormal spermatogenesis	Arhgdib<tm1Miyo>/Arhgdib<tm1Miyo>	involves: 129S/SvEv	N	17142749
MGI:3814726	M	MP:0001940	testis hypoplasia	Arhgdia<tm1Ytk>/Arhgdia<tm1Ytk>,Arhgdib<tm1Miyo>/Arhgdib<tm1Miyo>	involves: 129S/SvEv	N	17142749
MGI:3814726	M	MP:0001925	male infertility	Arhgdia<tm1Ytk>/Arhgdia<tm1Ytk>,Arhgdib<tm1Miyo>/Arhgdib<tm1Miyo>	involves: 129S/SvEv	N	17142749
MGI:3814825	F	MP:0005387	immune system phenotype	Btk<xid>/Btk<xid>	involves: C57BL/6 * CBA	Y	12634786
MGI:3814865	M	MP:0001925	male infertility	Hoxa11<tm1Dmwe>/Hoxa11<tm1Dmwe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18942146
MGI:3814865	F	MP:0001926	female infertility	Hoxa11<tm1Dmwe>/Hoxa11<tm1Dmwe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18942146
MGI:3814866	M	MP:0001925	male infertility	Hoxa11<tm1Dmwe>/Hoxa11<+>,Hoxc11<tm1Mrc>/Hoxc11<+>,Hoxd11<tm1Mrc>/Hoxd11<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	18942146
MGI:3814866	F	MP:0001926	female infertility	Hoxa11<tm1Dmwe>/Hoxa11<+>,Hoxc11<tm1Mrc>/Hoxc11<+>,Hoxd11<tm1Mrc>/Hoxd11<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	18942146
MGI:3814871	M	MP:0001925	male infertility	Hoxa11<tm1Mrc>/Hoxa11<+>,Hoxc11<tm1Mrc>/Hoxc11<+>,Hoxd11<tm1Mrc>/Hoxd11<+>	involves: 129S7/SvEvBrd	N	12050119
MGI:3814871	F	MP:0001926	female infertility	Hoxa11<tm1Mrc>/Hoxa11<+>,Hoxc11<tm1Mrc>/Hoxc11<+>,Hoxd11<tm1Mrc>/Hoxd11<+>	involves: 129S7/SvEvBrd	N	12050119
MGI:3814872	M	MP:0001925	male infertility	Hoxa11<tm1Mrc>/Hoxa11<tm1Mrc>,Hoxc11<tm1Mrc>/Hoxc11<+>,Hoxd11<tm1Mrc>/Hoxd11<+>	involves: 129S7/SvEvBrd	N	12050119
MGI:3814872	F	MP:0001926	female infertility	Hoxa11<tm1Mrc>/Hoxa11<tm1Mrc>,Hoxc11<tm1Mrc>/Hoxc11<+>,Hoxd11<tm1Mrc>/Hoxd11<+>	involves: 129S7/SvEvBrd	N	12050119
MGI:3814873	M	MP:0001925	male infertility	Hoxa11<tm1Mrc>/Hoxa11<+>,Hoxc11<tm1Mrc>/Hoxc11<tm1Mrc>,Hoxd11<tm1Mrc>/Hoxd11<+>	involves: 129S7/SvEvBrd	N	12050119
MGI:3814873	F	MP:0001926	female infertility	Hoxa11<tm1Mrc>/Hoxa11<+>,Hoxc11<tm1Mrc>/Hoxc11<tm1Mrc>,Hoxd11<tm1Mrc>/Hoxd11<+>	involves: 129S7/SvEvBrd	N	12050119
MGI:3814874	F	MP:0001926	female infertility	Hoxa11<tm1Mrc>/Hoxa11<+>,Hoxc11<tm1Mrc>/Hoxc11<+>,Hoxd11<tm1Mrc>/Hoxd11<tm1Mrc>	involves: 129S7/SvEvBrd	N	12050119
MGI:3814874	M	MP:0001925	male infertility	Hoxa11<tm1Mrc>/Hoxa11<+>,Hoxc11<tm1Mrc>/Hoxc11<+>,Hoxd11<tm1Mrc>/Hoxd11<tm1Mrc>	involves: 129S7/SvEvBrd	N	12050119
MGI:3815010	F	MP:0006271	abnormal involution of the mammary gland	Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>	involves: 129S1/Sv	N	27044867
MGI:3815017	M	MP:0004191	neuronal intranuclear inclusions	Fmr1<tm2Cgr>/Y	involves: 129P2/OlaHsd	N	12700164
MGI:3815018	M	MP:0031391	increased locomotor activity	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/J	N	26306459
MGI:3815018	M	MP:0009141	increased prepulse inhibition	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/J	N	14981523
MGI:3815018	M	MP:0001463	abnormal spatial learning	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/J	N	26306459
MGI:3815018	M	MP:0002063	abnormal learning/memory/conditioning	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/J	N	14981523
MGI:3815018	M	MP:0001486	abnormal startle reflex	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/J	N	14981523
MGI:3815018	M	MP:0001409	increased stereotypic behavior	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/J	N	26306459
MGI:3815018	M	MP:0002152	abnormal brain morphology	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/J	N	26306459
MGI:3815023	M	MP:0010053	decreased grip strength	Fmr1<tm2Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J * FVB	N	15876460
MGI:3815023	M	MP:0001405	impaired coordination	Fmr1<tm2Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J * FVB	N	15876460
MGI:3815023	M	MP:0004924	abnormal behavior	Fmr1<tm2Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J * FVB	N	15876460
MGI:3815023	M	MP:0002063	abnormal learning/memory/conditioning	Fmr1<tm2Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J * FVB	N	15876460
MGI:3815114	F	MP:0003546	decreased alcohol consumption	Ccl2<tm1Rol>/Ccl2<tm1Rol>	B6.129S4-Ccl2<tm1Rol>	N	16105698
MGI:3815114	F	MP:0002570	alcohol aversion	Ccl2<tm1Rol>/Ccl2<tm1Rol>	B6.129S4-Ccl2<tm1Rol>	N	16105698
MGI:3815142	M	MP:0001304	cataract	Cdkn2a<tm1Rdp>/Cdkn2a<+>,X/Tg(Tyr-HRAS)60Lc	involves: 129/Sv * C57BL/6J * CBA/J * FVB/N * SJL	N	17987514
MGI:3815142	M	MP:0004501	increased incidence of tumors by UV-induction	Cdkn2a<tm1Rdp>/Cdkn2a<+>,X/Tg(Tyr-HRAS)60Lc	involves: 129/Sv * C57BL/6J * CBA/J * FVB/N * SJL	N	17987514
MGI:3815142	M	MP:0010276	increased intraocular melanoma incidence	Cdkn2a<tm1Rdp>/Cdkn2a<+>,X/Tg(Tyr-HRAS)60Lc	involves: 129/Sv * C57BL/6J * CBA/J * FVB/N * SJL	N	17987514
MGI:3815191	F	MP:0002169	no abnormal phenotype detected	Hprt1<tm1(Nfkb1-EGFP)Cjo>/Hprt1<+>	involves: 129P2/OlaHsd * C57BL/6	N	15265883
MGI:3815192	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm1(Nfkb1-EGFP)Cjo>/Y	involves: 129P2/OlaHsd * C57BL/6	N	15265883
MGI:3815298	M	MP:0002674	abnormal sperm motility	Prm3<tm1Grz>/Prm3<tm1Grz>	involves: 129/Sv * C57BL/6	N	18256328
MGI:3815458	F	MP:0001923	reduced female fertility	Nr1d1<tm1Ven>/Nr1d1<tm1Ven>	Not Specified	N	10704394
MGI:3817185	M	MP:0003631	nervous system phenotype	Mecp2<tm1.1Bird>/Y,Tg(MECP2)1Hzo/0	involves: 129P2/OlaHsd * FVB	Y	17920015
MGI:3817185	M	MP:0005386	behavior/neurological phenotype	Mecp2<tm1.1Bird>/Y,Tg(MECP2)1Hzo/0	involves: 129P2/OlaHsd * FVB	Y	15351775
MGI:3817185	M	MP:0010768	mortality/aging	Mecp2<tm1.1Bird>/Y,Tg(MECP2)1Hzo/0	involves: 129P2/OlaHsd * FVB	Y	15351775
MGI:3817230	M	MP:0003631	nervous system phenotype	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd	Y	17920015
MGI:3817230	M	MP:0012006	abnormal hippocampus physiology	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd	N	24735673
MGI:3817230	M	MP:0004998	decreased CNS synapse formation	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd	N	17920015
MGI:3817230	M	MP:0011270	decreased excitatory postsynaptic current amplitude	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd	N	17920015
MGI:3817230	M	MP:0004792	abnormal synaptic vesicle number	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd	N	17920015
MGI:3817230	M	MP:0014376	decreased miniature excitatory postsynaptic current frequency	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd	N	17920015
MGI:3817230	M	MP:0003633	abnormal nervous system physiology	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd	N	24735673
MGI:3817236	F	MP:0008948	decreased neuron number	Mecp2<tm1.1Bird>/Mecp2<+>	involves: 129P2/OlaHsd	N	16549272
MGI:3817236	F	MP:0000788	abnormal cerebral cortex morphology	Mecp2<tm1.1Bird>/Mecp2<+>	involves: 129P2/OlaHsd	N	23452848
MGI:3817236	F	MP:0000807	abnormal hippocampus morphology	Mecp2<tm1.1Bird>/Mecp2<+>	involves: 129P2/OlaHsd	N	23452848
MGI:3817236	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Mecp2<tm1.1Bird>/Mecp2<+>	involves: 129P2/OlaHsd	N	16549272
MGI:3817273	M	MP:0008908	increased total fat pad weight	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	18321865
MGI:3817273	M	MP:0001260	increased body weight	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	18321865
MGI:3817273	M	MP:0001360	abnormal social investigation	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	18321865
MGI:3817273	M	MP:0001513	limb grasping	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	18321865
MGI:3817273	M	MP:0001261	obese	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	18321865
MGI:3817273	M	MP:0005386	behavior/neurological phenotype	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6 * CBA	Y	18321865
MGI:3817273	M	MP:0001516	abnormal motor coordination/balance	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	18321865
MGI:3817326	M	MP:0002566	abnormal sexual interaction	Kcnn2<m1Btlr>/Kcnn2<m1Btlr>	C57BL/6J-Kcnn2<m1Btlr>	N	MGI:3799662
MGI:3817411	M	MP:0001147	small testis	Pcna<tm1.1Mdsc>/Pcna<tm1.1Mdsc>,Tg(Pcna*K164R)1Mdsc/0	involves: FVB/N	N	18854411
MGI:3817411	M	MP:0001155	arrest of spermatogenesis	Pcna<tm1.1Mdsc>/Pcna<tm1.1Mdsc>,Tg(Pcna*K164R)1Mdsc/0	involves: FVB/N	N	18854411
MGI:3817454	F	MP:0004834	ovary hemorrhage	Arid4a<tm1Alb>/Arid4a<tm1Alb>	involves: 129S7/SvEvBrd	N	18728284
MGI:3817461	M	MP:0010768	mortality/aging	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x C57BL/6)F1	Y	18321864
MGI:3817461	M	MP:0001489	decreased startle reflex	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x C57BL/6)F1	N	18321864
MGI:3817461	M	MP:0009142	decreased prepulse inhibition	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x C57BL/6)F1	N	18321864
MGI:3817461	M	MP:0001405	impaired coordination	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x C57BL/6)F1	N	18321864
MGI:3817461	M	MP:0001360	abnormal social investigation	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x C57BL/6)F1	N	18321864
MGI:3817461	M	MP:0001447	abnormal nest building behavior	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x C57BL/6)F1	N	18321864
MGI:3817461	M	MP:0001260	increased body weight	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x C57BL/6)F1	N	18321864
MGI:3817461	M	MP:0001973	increased thermal nociceptive threshold	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x C57BL/6)F1	N	18321864
MGI:3817461	M	MP:0001968	abnormal touch/ nociception	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x C57BL/6)F1	N	18321864
MGI:3817462	M	MP:0001968	abnormal touch/ nociception	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x FVB/N)F1	N	18321864
MGI:3817462	M	MP:0001957	apnea	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x FVB/N)F1	N	18321864
MGI:3817462	M	MP:0001951	abnormal breathing pattern	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x FVB/N)F1	N	18321864
MGI:3817462	M	MP:0005386	behavior/neurological phenotype	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x FVB/N)F1	Y	18321864
MGI:3817462	M	MP:0001469	abnormal contextual conditioning behavior	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x FVB/N)F1	N	18321864
MGI:3817462	M	MP:0001454	abnormal cued conditioning behavior	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x FVB/N)F1	N	18321864
MGI:3817462	M	MP:0001364	decreased anxiety-related response	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x FVB/N)F1	N	18321864
MGI:3817462	M	MP:0009142	decreased prepulse inhibition	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x FVB/N)F1	N	18321864
MGI:3817462	M	MP:0005378	growth/size/body region phenotype	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x FVB/N)F1	Y	18321864
MGI:3817462	M	MP:0010768	mortality/aging	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x FVB/N)F1	Y	18321864
MGI:3817462	M	MP:0001360	abnormal social investigation	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x FVB/N)F1	N	18321864
MGI:3817462	M	MP:0002574	increased vertical activity	Mecp2<tm1Bird>/Y	(129S6.129P2-Mecp2<tm1Bird> x FVB/N)F1	N	18321864
MGI:3817537	F	MP:0004856	decreased ovary weight	Galp<tm1Stei>/Galp<tm1Stei>	involves: 129	N	18775887
MGI:3817750	F	MP:0004936	impaired branching involved in ureteric bud morphogenesis	Gpc3<tm1Fil>/Gpc3<tm1Fil>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3817750	F	MP:0006032	abnormal ureteric bud morphology	Gpc3<tm1Fil>/Gpc3<tm1Fil>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3817750	F	MP:0003315	abnormal perineum morphology	Gpc3<tm1Fil>/Gpc3<tm1Fil>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3817750	F	MP:0002412	increased susceptibility to bacterial infection	Gpc3<tm1Fil>/Gpc3<tm1Fil>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3817750	F	MP:0000527	abnormal kidney development	Gpc3<tm1Fil>/Gpc3<tm1Fil>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3817750	F	MP:0011086	postnatal lethality, incomplete penetrance	Gpc3<tm1Fil>/Gpc3<tm1Fil>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3817750	F	MP:0003675	kidney cyst	Gpc3<tm1Fil>/Gpc3<tm1Fil>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3817750	F	MP:0001123	dilated uterus	Gpc3<tm1Fil>/Gpc3<tm1Fil>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3817750	F	MP:0001861	lung inflammation	Gpc3<tm1Fil>/Gpc3<tm1Fil>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3817750	F	MP:0000460	mandible hypoplasia	Gpc3<tm1Fil>/Gpc3<tm1Fil>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3817750	F	MP:0001144	vagina atresia	Gpc3<tm1Fil>/Gpc3<tm1Fil>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3817750	F	MP:0001260	increased body weight	Gpc3<tm1Fil>/Gpc3<tm1Fil>	B6.Cg-Gpc3<tm1Fil>	N	10402475
MGI:3817856	M	MP:0003936	abnormal reproductive system development	Foxp3<m1Btlr>/Y	C57BL/6J-Foxp3<m1Btlr>	N	MGI:3817751
MGI:3817856	M	MP:0003853	dry skin	Foxp3<m1Btlr>/Y	C57BL/6J-Foxp3<m1Btlr>	N	MGI:3817751
MGI:3817856	M	MP:0001265	decreased body size	Foxp3<m1Btlr>/Y	C57BL/6J-Foxp3<m1Btlr>	N	MGI:3817751
MGI:3817856	M	MP:0005159	azoospermia	Foxp3<m1Btlr>/Y	C57BL/6J-Foxp3<m1Btlr>	N	MGI:3817751
MGI:3817856	M	MP:0002083	premature death	Foxp3<m1Btlr>/Y	C57BL/6J-Foxp3<m1Btlr>	N	MGI:3817751
MGI:3817856	M	MP:0001192	scaly skin	Foxp3<m1Btlr>/Y	C57BL/6J-Foxp3<m1Btlr>	N	MGI:3817751
MGI:3817856	M	MP:0001212	skin lesions	Foxp3<m1Btlr>/Y	C57BL/6J-Foxp3<m1Btlr>	N	MGI:3817751
MGI:3817856	M	MP:0000414	alopecia	Foxp3<m1Btlr>/Y	C57BL/6J-Foxp3<m1Btlr>	N	MGI:3817751
MGI:3817866	F	MP:0002169	no abnormal phenotype detected	Foxp3<m1Btlr>/Foxp3<+>	C57BL/6J-Foxp3<m1Btlr>	N	MGI:3817751
MGI:3817867	F	MP:0010768	mortality/aging	Foxp3<m1Btlr>/Foxp3<m1Btlr>	C57BL/6J-Foxp3<m1Btlr>	Y	MGI:3817751
MGI:3817878	F	MP:0001861	lung inflammation	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Rag2<tm1Fwa>/Rag2<tm1Fwa>	involves: 129S/SvEv * 129S4/SvJae	N	17082625
MGI:3817878	F	MP:0008070	absent T cells	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Rag2<tm1Fwa>/Rag2<tm1Fwa>	involves: 129S/SvEv * 129S4/SvJae	N	17082625
MGI:3817878	F	MP:0009763	increased susceptibility to induced morbidity/mortality	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Rag2<tm1Fwa>/Rag2<tm1Fwa>	involves: 129S/SvEv * 129S4/SvJae	N	17082625
MGI:3817878	F	MP:0008555	abnormal interferon secretion	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Rag2<tm1Fwa>/Rag2<tm1Fwa>	involves: 129S/SvEv * 129S4/SvJae	N	17082625
MGI:3817878	F	MP:0002412	increased susceptibility to bacterial infection	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Rag2<tm1Fwa>/Rag2<tm1Fwa>	involves: 129S/SvEv * 129S4/SvJae	N	17082625
MGI:3817878	F	MP:0008046	absent NK cells	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Rag2<tm1Fwa>/Rag2<tm1Fwa>	involves: 129S/SvEv * 129S4/SvJae	N	17082625
MGI:3818299	F	MP:0000367	abnormal coat/ hair morphology	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818299	F	MP:0013370	anhidrosis	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818299	F	MP:0000125	absent incisors	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818299	F	MP:0000422	delayed hair appearance	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818299	F	MP:0003704	abnormal hair follicle development	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818299	F	MP:0006363	absent auchene hairs	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818299	F	MP:0030457	abnormal molar cusp morphology	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818299	F	MP:0000414	alopecia	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818299	F	MP:0006367	absent sweat gland	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818299	F	MP:0002100	abnormal tooth morphology	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818299	F	MP:0006366	absent zigzag hairs	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818299	F	MP:0000400	abnormal awl hair morphology	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818299	F	MP:0006400	decreased molar number	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818299	F	MP:0006365	absent guard hair	Eda<Ta>/Eda<Ta>,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0000367	abnormal coat/ hair morphology	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0006366	absent zigzag hairs	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0006365	absent guard hair	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0000414	alopecia	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0006400	decreased molar number	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0000400	abnormal awl hair morphology	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0006363	absent auchene hairs	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0030457	abnormal molar cusp morphology	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0000125	absent incisors	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0003704	abnormal hair follicle development	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0000422	delayed hair appearance	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0013370	anhidrosis	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0006367	absent sweat gland	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818300	M	MP:0002100	abnormal tooth morphology	Eda<Ta>/Y,Tnfrsf19<Gt(OST294987)Lex>/Tnfrsf19<Gt(OST294987)Lex>	involves: 129S5/SvEvBrd * A * C57BL/6 * CBA/CaGnLe	N	18689798
MGI:3818314	M	MP:0001145	abnormal male reproductive system morphology	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818314	M	MP:0006379	abnormal spermatocyte morphology	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818314	M	MP:0001147	small testis	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818314	M	MP:0005169	abnormal male meiosis	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818314	M	MP:0014052	increased male germ cell apoptosis	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818314	M	MP:0001156	abnormal spermatogenesis	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818314	M	MP:0001153	small seminiferous tubules	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818314	M	MP:0006380	abnormal spermatid morphology	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818314	M	MP:0001925	male infertility	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818314	F	MP:0004805	absent oocytes	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818314	F	MP:0001127	small ovary	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818314	F	MP:0001119	abnormal female reproductive system morphology	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818314	F	MP:0002777	absent ovarian follicles	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818314	F	MP:0001926	female infertility	Cdk1<tm1(Cdk2)Kald>/Cdk1<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	N	18787066
MGI:3818315	M	MP:0005169	abnormal male meiosis	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv	N	18787066
MGI:3818417	F	MP:0004256	abnormal maternal decidual layer morphology	Hcst<tm1.1Cln>/Hcst<tm1.1Cln>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818417	F	MP:0008876	decreased uterine NK cell number	Hcst<tm1.1Cln>/Hcst<tm1.1Cln>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818417	F	MP:0012529	abnormal decidua basalis morphology	Hcst<tm1.1Cln>/Hcst<tm1.1Cln>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818418	F	MP:0004256	abnormal maternal decidual layer morphology	Tyrobp<tm1.1Viv>/Tyrobp<tm1.1Viv>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818418	F	MP:0012726	abnormal uterine spiral artery morphology	Tyrobp<tm1.1Viv>/Tyrobp<tm1.1Viv>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818418	F	MP:0012529	abnormal decidua basalis morphology	Tyrobp<tm1.1Viv>/Tyrobp<tm1.1Viv>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818418	F	MP:0012727	abnormal uterine spiral artery remodeling	Tyrobp<tm1.1Viv>/Tyrobp<tm1.1Viv>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818418	F	MP:0001728	failure of embryo implantation	Tyrobp<tm1.1Viv>/Tyrobp<tm1.1Viv>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818418	F	MP:0008876	decreased uterine NK cell number	Tyrobp<tm1.1Viv>/Tyrobp<tm1.1Viv>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818419	F	MP:0012727	abnormal uterine spiral artery remodeling	Cd247<tm1Mhu>/Cd247<tm1Mhu>,Fcer1g<tm1Rav>/Fcer1g<tm1Rav>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	N	15878887
MGI:3818419	F	MP:0008876	decreased uterine NK cell number	Cd247<tm1Mhu>/Cd247<tm1Mhu>,Fcer1g<tm1Rav>/Fcer1g<tm1Rav>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	N	15878887
MGI:3818419	F	MP:0012529	abnormal decidua basalis morphology	Cd247<tm1Mhu>/Cd247<tm1Mhu>,Fcer1g<tm1Rav>/Fcer1g<tm1Rav>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	N	15878887
MGI:3818419	F	MP:0012726	abnormal uterine spiral artery morphology	Cd247<tm1Mhu>/Cd247<tm1Mhu>,Fcer1g<tm1Rav>/Fcer1g<tm1Rav>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	N	15878887
MGI:3818419	F	MP:0004256	abnormal maternal decidual layer morphology	Cd247<tm1Mhu>/Cd247<tm1Mhu>,Fcer1g<tm1Rav>/Fcer1g<tm1Rav>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	N	15878887
MGI:3818420	F	MP:0008876	decreased uterine NK cell number	Fcer1g<tm1Rav>/Fcer1g<tm1Rav>,Tyrobp<tm1.1Viv>/Tyrobp<tm1.1Viv>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818420	F	MP:0012726	abnormal uterine spiral artery morphology	Fcer1g<tm1Rav>/Fcer1g<tm1Rav>,Tyrobp<tm1.1Viv>/Tyrobp<tm1.1Viv>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818420	F	MP:0012727	abnormal uterine spiral artery remodeling	Fcer1g<tm1Rav>/Fcer1g<tm1Rav>,Tyrobp<tm1.1Viv>/Tyrobp<tm1.1Viv>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818420	F	MP:0012529	abnormal decidua basalis morphology	Fcer1g<tm1Rav>/Fcer1g<tm1Rav>,Tyrobp<tm1.1Viv>/Tyrobp<tm1.1Viv>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818420	F	MP:0004256	abnormal maternal decidual layer morphology	Fcer1g<tm1Rav>/Fcer1g<tm1Rav>,Tyrobp<tm1.1Viv>/Tyrobp<tm1.1Viv>	involves: 129P2/OlaHsd * C57BL/6	N	15878887
MGI:3818472	F	MP:0000662	abnormal branching of the mammary ductal tree	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * C57BL/6N	N	11861370
MGI:3818681	M	MP:0001922	reduced male fertility	Rhcg<tm1Ibmm>/Rhcg<tm1Ibmm>	involves: 129P2/OlaHsd * CD-1	N	19020613
MGI:3818681	M	MP:0002631	abnormal epididymis morphology	Rhcg<tm1Ibmm>/Rhcg<tm1Ibmm>	involves: 129P2/OlaHsd * CD-1	N	19020613
MGI:3818928	F	MP:0001274	curly vibrissae	Atp7a<Mo-dp2>/Atp7a<+>	Not Specified	N	MGI:61313
MGI:3818928	F	MP:0001524	impaired limb coordination	Atp7a<Mo-dp2>/Atp7a<+>	Not Specified	N	MGI:61313
MGI:3818928	F	MP:0008731	abnormal hair shaft melanin granule morphology	Atp7a<Mo-dp2>/Atp7a<+>	Not Specified	N	MGI:61313
MGI:3818928	F	MP:0002082	postnatal lethality	Atp7a<Mo-dp2>/Atp7a<+>	Not Specified	N	MGI:61313
MGI:3818928	F	MP:0003198	calcified tendon	Atp7a<Mo-dp2>/Atp7a<+>	Not Specified	N	MGI:61313
MGI:3818928	F	MP:0000410	waved hair	Atp7a<Mo-dp2>/Atp7a<+>	Not Specified	N	MGI:61313
MGI:3818928	F	MP:0000421	mottled coat	Atp7a<Mo-dp2>/Atp7a<+>	Not Specified	N	MGI:61313
MGI:3818928	F	MP:0000137	abnormal vertebrae morphology	Atp7a<Mo-dp2>/Atp7a<+>	Not Specified	N	MGI:61313
MGI:3818928	F	MP:0000572	abnormal autopod morphology	Atp7a<Mo-dp2>/Atp7a<+>	Not Specified	N	MGI:61313
MGI:3818928	F	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-dp2>/Atp7a<+>	Not Specified	N	MGI:61313
MGI:3818928	F	MP:0002074	abnormal hair texture	Atp7a<Mo-dp2>/Atp7a<+>	Not Specified	N	MGI:61313
MGI:3818928	F	MP:0005508	abnormal skeleton morphology	Atp7a<Mo-dp2>/Atp7a<+>	Not Specified	N	MGI:61313
MGI:3818929	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Atp7a<Mo-dp2>/Y	Not Specified	N	MGI:61313
MGI:3818929	M	MP:0001722	pale yolk sac	Atp7a<Mo-dp2>/Y	Not Specified	N	MGI:61313
MGI:3818988	M	MP:0001925	male infertility	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	either: (involves: CD-1) or (involves: 129X1/SvJ * C57BL/6)	N	17307907
MGI:3818988	M	MP:0002687	oligozoospermia	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	either: (involves: CD-1) or (involves: 129X1/SvJ * C57BL/6)	N	17307907
MGI:3818988	M	MP:0009243	hairpin sperm flagellum	Fkbp4<tm1Dvds>/Fkbp4<tm1Dvds>	either: (involves: CD-1) or (involves: 129X1/SvJ * C57BL/6)	N	17307907
MGI:3819122	F	MP:0001923	reduced female fertility	Kitl<Sl-1Neu>/Kitl<Sl-1Neu>	involves: 102/El * C3H/El	N	8875893
MGI:3819124	F	MP:0001926	female infertility	Kitl<Sl-2Neu>/Kitl<Sl-2Neu>	involves: 102/El * C3H/El	N	8875893
MGI:3819124	M	MP:0001922	reduced male fertility	Kitl<Sl-2Neu>/Kitl<Sl-2Neu>	involves: 102/El * C3H/El	N	8875893
MGI:3819126	F	MP:0001923	reduced female fertility	Kitl<Sl-3Neu>/Kitl<Sl-3Neu>	involves: 102/El * C3H/El	N	9360640
MGI:3819129	M	MP:0002631	abnormal epididymis morphology	Nckap1l<m1Iri>/Nckap1l<m1Iri>	involves: C57BL/6	N	19015308
MGI:3819267	F	MP:0001923	reduced female fertility	Chrna7<tm1Bay>/Chrna7<tm1Bay>	B6.129S7-Chrna7<tm1Bay>/J	N	15364017
MGI:3819267	F	MP:0009006	prolonged estrous cycle	Chrna7<tm1Bay>/Chrna7<tm1Bay>	B6.129S7-Chrna7<tm1Bay>/J	N	15364017
MGI:3819267	M	MP:0002675	asthenozoospermia	Chrna7<tm1Bay>/Chrna7<tm1Bay>	B6.129S7-Chrna7<tm1Bay>/J	N	15944242
MGI:3819267	M	MP:0014370	impaired spatial working memory	Chrna7<tm1Bay>/Chrna7<tm1Bay>	B6.129S7-Chrna7<tm1Bay>/J	N	16923147
MGI:3819271	M	MP:0002843	decreased systemic arterial blood pressure	Gna11<tm1Soff>/Gna11<tm1Soff>,Gnaq<tm2Soff>/Gnaq<tm2Soff>,X/Tg(Myh11-icre/ERT2)1Soff	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	N	18084302
MGI:3819271	M	MP:0003026	decreased vasoconstriction	Gna11<tm1Soff>/Gna11<tm1Soff>,Gnaq<tm2Soff>/Gnaq<tm2Soff>,X/Tg(Myh11-icre/ERT2)1Soff	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	N	18084302
MGI:3819271	M	MP:0004876	decreased mean systemic arterial blood pressure	Gna11<tm1Soff>/Gna11<tm1Soff>,Gnaq<tm2Soff>/Gnaq<tm2Soff>,X/Tg(Myh11-icre/ERT2)1Soff	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	N	18084302
MGI:3819345	M	MP:0003026	decreased vasoconstriction	Gna12<tm1Citb>/Gna12<tm1Citb>,Gna13<tm2.1Soff>/Gna13<tm2.1Soff>,X/Tg(Myh11-icre/ERT2)1Soff	involves: 129S1/Sv * FVB/N	N	18084302
MGI:3819345	M	MP:0002843	decreased systemic arterial blood pressure	Gna12<tm1Citb>/Gna12<tm1Citb>,Gna13<tm2.1Soff>/Gna13<tm2.1Soff>,X/Tg(Myh11-icre/ERT2)1Soff	involves: 129S1/Sv * FVB/N	N	18084302
MGI:3819380	M	MP:0001158	abnormal prostate gland morphology	Nog<tm1Amc>/Nog<tm1Amc>	involves: 129S1/Sv * C57BL/6J * ICR	N	18028901
MGI:3819380	M	MP:0009735	abnormal prostate gland development	Nog<tm1Amc>/Nog<tm1Amc>	involves: 129S1/Sv * C57BL/6J * ICR	N	18028901
MGI:3819380	M	MP:0002770	absent bulbourethral gland	Nog<tm1Amc>/Nog<tm1Amc>	involves: 129S1/Sv * C57BL/6J * ICR	N	18028901
MGI:3819380	M	MP:0001145	abnormal male reproductive system morphology	Nog<tm1Amc>/Nog<tm1Amc>	involves: 129S1/Sv * C57BL/6J * ICR	N	18028901
MGI:3819380	M	MP:0002286	cryptorchism	Nog<tm1Amc>/Nog<tm1Amc>	involves: 129S1/Sv * C57BL/6J * ICR	N	18028901
MGI:3819381	M	MP:0031362	decreased prostate gland ventral lobe weight	Nog<tm1Amc>/Nog<+>	involves: 129S1/Sv * C57BL/6J * ICR	N	18028901
MGI:3819421	F	MP:0010299	increased mammary gland tumor incidence	T(9;17)138Ca/T(9;17)138Ca	Not Specified	N	MGI:4940633
MGI:3819783	F	MP:0001923	reduced female fertility	Dh/Dh<+>,H2<d>/H2<d>	NZB.Cg-Dh	N	310848
MGI:3819783	M	MP:0002286	cryptorchism	Dh/Dh<+>,H2<d>/H2<d>	NZB.Cg-Dh	N	310848
MGI:3819797	M	MP:0001922	reduced male fertility	Hoxa10<tm1Ipc>/Hoxa10<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	7667266
MGI:3819797	M	MP:0001154	seminiferous tubule degeneration	Hoxa10<tm1Ipc>/Hoxa10<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	7667266
MGI:3819797	M	MP:0005159	azoospermia	Hoxa10<tm1Ipc>/Hoxa10<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	7667266
MGI:3819797	M	MP:0001147	small testis	Hoxa10<tm1Ipc>/Hoxa10<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	7667266
MGI:3819797	M	MP:0009213	absent male inguinal canal	Hoxa10<tm1Ipc>/Hoxa10<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	7667266
MGI:3819797	M	MP:0002784	abnormal Sertoli cell morphology	Hoxa10<tm1Ipc>/Hoxa10<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	7667266
MGI:3819797	M	MP:0002670	absent scrotum	Hoxa10<tm1Ipc>/Hoxa10<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	7667266
MGI:3819797	F	MP:0001923	reduced female fertility	Hoxa10<tm1Ipc>/Hoxa10<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	7667266
MGI:3819797	M	MP:0001925	male infertility	Hoxa10<tm1Ipc>/Hoxa10<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	7667266
MGI:3819797	M	MP:0002286	cryptorchism	Hoxa10<tm1Ipc>/Hoxa10<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	7667266
MGI:3819797	F	MP:0009082	uterus cyst	Hoxa10<tm1Ipc>/Hoxa10<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	7667266
MGI:3819797	M	MP:0001156	abnormal spermatogenesis	Hoxa10<tm1Ipc>/Hoxa10<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	N	7667266
MGI:3819955	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Ggamma-T)15Cps/Tg(Ggamma-T)15Cps	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819955	M	MP:0014237	decreased tumor-free survival time	Tg(Ggamma-T)15Cps/Tg(Ggamma-T)15Cps	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819955	M	MP:0002031	increased adrenal gland tumor incidence	Tg(Ggamma-T)15Cps/Tg(Ggamma-T)15Cps	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819955	M	MP:0009552	urinary bladder obstruction	Tg(Ggamma-T)15Cps/Tg(Ggamma-T)15Cps	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819955	M	MP:0010357	increased prostate gland tumor incidence	Tg(Ggamma-T)15Cps/Tg(Ggamma-T)15Cps	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819955	M	MP:0010344	increased hibernoma incidence	Tg(Ggamma-T)15Cps/Tg(Ggamma-T)15Cps	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819955	M	MP:0006262	increased testis tumor incidence	Tg(Ggamma-T)15Cps/Tg(Ggamma-T)15Cps	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819956	M	MP:0006262	increased testis tumor incidence	Tg(Ggamma-T)15Cps/0	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819956	M	MP:0002031	increased adrenal gland tumor incidence	Tg(Ggamma-T)15Cps/0	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819956	M	MP:0010357	increased prostate gland tumor incidence	Tg(Ggamma-T)15Cps/0	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819956	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Ggamma-T)15Cps/0	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819956	M	MP:0010344	increased hibernoma incidence	Tg(Ggamma-T)15Cps/0	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819956	M	MP:0009552	urinary bladder obstruction	Tg(Ggamma-T)15Cps/0	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819956	M	MP:0014237	decreased tumor-free survival time	Tg(Ggamma-T)15Cps/0	involves: C57BL/6J * CBA/J	N	9041192
MGI:3819969	F	MP:0003845	abnormal decidualization	Src<tm1Sor>/Src<tm1Sor>	B6.129S7-Src<tm1Sor>/J	N	16107610
MGI:3819969	F	MP:0001926	female infertility	Src<tm1Sor>/Src<tm1Sor>	B6.129S7-Src<tm1Sor>/J	N	16107610
MGI:3820079	F	MP:0001927	abnormal estrous cycle	Ntf3<tm1Tojo>/Ntf3<tm1Tojo>	involves: C57BL/6 * DBA/2 * ICR	N	7712171
MGI:3820079	F	MP:0001926	female infertility	Ntf3<tm1Tojo>/Ntf3<tm1Tojo>	involves: C57BL/6 * DBA/2 * ICR	N	7712171
MGI:3820221	F	MP:0001120	abnormal uterus morphology	Igf2r<tm2Arge>/Igf2r<+>	involves: 129	N	8806828
MGI:3820221	F	MP:0001144	vagina atresia	Igf2r<tm2Arge>/Igf2r<+>	involves: 129	N	8806828
MGI:3820221	M	MP:0001922	reduced male fertility	Igf2r<tm2Arge>/Igf2r<+>	involves: 129	N	8806828
MGI:3820221	F	MP:0001923	reduced female fertility	Igf2r<tm2Arge>/Igf2r<+>	involves: 129	N	8806828
MGI:3820221	F	MP:0004906	enlarged uterus	Igf2r<tm2Arge>/Igf2r<+>	involves: 129	N	8806828
MGI:3820222	F	MP:0001120	abnormal uterus morphology	Igf2r<tm1Arge>/Igf2r<+>	involves: 129	N	8806828
MGI:3820222	F	MP:0004906	enlarged uterus	Igf2r<tm1Arge>/Igf2r<+>	involves: 129	N	8806828
MGI:3820222	M	MP:0001922	reduced male fertility	Igf2r<tm1Arge>/Igf2r<+>	involves: 129	N	8806828
MGI:3820222	F	MP:0001144	vagina atresia	Igf2r<tm1Arge>/Igf2r<+>	involves: 129	N	8806828
MGI:3820222	F	MP:0001923	reduced female fertility	Igf2r<tm1Arge>/Igf2r<+>	involves: 129	N	8806828
MGI:3820223	F	MP:0001923	reduced female fertility	Igf2r<tm2Arge>/Igf2r<tm2Arge>	involves: 129	N	8806828
MGI:3820223	F	MP:0001144	vagina atresia	Igf2r<tm2Arge>/Igf2r<tm2Arge>	involves: 129	N	8806828
MGI:3820223	F	MP:0004906	enlarged uterus	Igf2r<tm2Arge>/Igf2r<tm2Arge>	involves: 129	N	8806828
MGI:3820223	M	MP:0001922	reduced male fertility	Igf2r<tm2Arge>/Igf2r<tm2Arge>	involves: 129	N	8806828
MGI:3820223	F	MP:0001120	abnormal uterus morphology	Igf2r<tm2Arge>/Igf2r<tm2Arge>	involves: 129	N	8806828
MGI:3820224	F	MP:0001923	reduced female fertility	Igf2r<tm1Arge>/Igf2r<tm1Arge>	involves: 129	N	8806828
MGI:3820224	M	MP:0001922	reduced male fertility	Igf2r<tm1Arge>/Igf2r<tm1Arge>	involves: 129	N	8806828
MGI:3820224	F	MP:0001144	vagina atresia	Igf2r<tm1Arge>/Igf2r<tm1Arge>	involves: 129	N	8806828
MGI:3820224	F	MP:0001120	abnormal uterus morphology	Igf2r<tm1Arge>/Igf2r<tm1Arge>	involves: 129	N	8806828
MGI:3820224	F	MP:0004906	enlarged uterus	Igf2r<tm1Arge>/Igf2r<tm1Arge>	involves: 129	N	8806828
MGI:3820230	M	MP:0002675	asthenozoospermia	Spag9<tm1Ysok>/Spag9<tm1Ysok>	involves: 129P2/OlaHsd * C57BL/6J	N	18574703
MGI:3820230	M	MP:0001922	reduced male fertility	Spag9<tm1Ysok>/Spag9<tm1Ysok>	involves: 129P2/OlaHsd * C57BL/6J	N	18574703
MGI:3820230	M	MP:0002687	oligozoospermia	Spag9<tm1Ysok>/Spag9<tm1Ysok>	involves: 129P2/OlaHsd * C57BL/6J	N	18574703
MGI:3820236	F	MP:0001386	abnormal maternal nurturing	Igf1r<tm1Arge>/Igf1r<tm1Arge>,Igf2r<tm2Arge>/Igf2r<tm2Arge>	involves: 129/Sv * 129S/SvEv	N	8806828
MGI:3820237	F	MP:0001386	abnormal maternal nurturing	Igf1r<tm1Arge>/Igf1r<tm1Arge>,Igf2r<tm1Arge>/Igf2r<tm1Arge>	involves: 129/Sv * 129S/SvEv	N	8806828
MGI:3820238	F	MP:0001386	abnormal maternal nurturing	Igf1r<tm1Arge>/Igf1r<tm1Arge>,Igf2r<tm2Arge>/Igf2r<+>	involves: 129/Sv * 129S/SvEv	N	8806828
MGI:3820239	F	MP:0001386	abnormal maternal nurturing	Igf1r<tm1Arge>/Igf1r<tm1Arge>,Igf2r<tm1Arge>/Igf2r<+>	involves: 129/Sv * 129S/SvEv	N	8806828
MGI:3820240	F	MP:0004853	abnormal ovary size	Ebf2<tm1Ggc>/Ebf2<tm1Ggc>	either: (involves: 129S2/SvPas * 129X1/SvJ) or (involves: 129S2/SvPas * C57BL/6J)	N	12466206
MGI:3820240	M	MP:0002631	abnormal epididymis morphology	Ebf2<tm1Ggc>/Ebf2<tm1Ggc>	either: (involves: 129S2/SvPas * 129X1/SvJ) or (involves: 129S2/SvPas * C57BL/6J)	N	12466206
MGI:3820240	M	MP:0001940	testis hypoplasia	Ebf2<tm1Ggc>/Ebf2<tm1Ggc>	either: (involves: 129S2/SvPas * 129X1/SvJ) or (involves: 129S2/SvPas * C57BL/6J)	N	12466206
MGI:3820240	M	MP:0001146	abnormal testis morphology	Ebf2<tm1Ggc>/Ebf2<tm1Ggc>	either: (involves: 129S2/SvPas * 129X1/SvJ) or (involves: 129S2/SvPas * C57BL/6J)	N	12466206
MGI:3820240	M	MP:0002216	abnormal seminiferous tubule morphology	Ebf2<tm1Ggc>/Ebf2<tm1Ggc>	either: (involves: 129S2/SvPas * 129X1/SvJ) or (involves: 129S2/SvPas * C57BL/6J)	N	12466206
MGI:3820250	M	MP:0001925	male infertility	Tim<T(4;17)3Lws>/Tim<+>	involves: C57BL/6J * DBA/2J	N	2320026
MGI:3820315	M	MP:0002882	abnormal neuron morphology	Arhgef9<tm1Betz>/Y,Tg(Camk2a-cre)2834Lusc/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	18625319
MGI:3820316	M	MP:0002882	abnormal neuron morphology	Arhgef9<tm1Betz>/Y,Emx1<tm1(cre)Yql>/Emx1<+>	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	N	18625319
MGI:3820400	F	MP:0001144	vagina atresia	Igf2r<tm1Stw>/Igf2r<+>	involves: 129S1/Sv * C57BL/6	N	8001817
MGI:3820400	F	MP:0004906	enlarged uterus	Igf2r<tm1Stw>/Igf2r<+>	involves: 129S1/Sv * C57BL/6	N	8001817
MGI:3820400	F	MP:0008258	thin endometrium	Igf2r<tm1Stw>/Igf2r<+>	involves: 129S1/Sv * C57BL/6	N	8001817
MGI:3820400	F	MP:0003126	abnormal external female genitalia morphology	Igf2r<tm1Stw>/Igf2r<+>	involves: 129S1/Sv * C57BL/6	N	8001817
MGI:3820400	F	MP:0001926	female infertility	Igf2r<tm1Stw>/Igf2r<+>	involves: 129S1/Sv * C57BL/6	N	8001817
MGI:3820400	F	MP:0009097	absent endometrial glands	Igf2r<tm1Stw>/Igf2r<+>	involves: 129S1/Sv * C57BL/6	N	8001817
MGI:3820400	M	MP:0001922	reduced male fertility	Igf2r<tm1Stw>/Igf2r<+>	involves: 129S1/Sv * C57BL/6	N	8001817
MGI:3820401	M	MP:0011087	neonatal lethality, complete penetrance	Gata1<tm4Sho>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12077323
MGI:3820401	M	MP:0000245	abnormal erythropoiesis	Gata1<tm4Sho>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12077323
MGI:3820401	M	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Gata1<tm4Sho>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12077323
MGI:3820401	M	MP:0000229	abnormal megakaryocyte differentiation	Gata1<tm4Sho>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12077323
MGI:3820401	M	MP:0001577	anemia	Gata1<tm4Sho>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12077323
MGI:3820401	M	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm4Sho>/Y	involves: 129S6/SvEvTac * C57BL/6	N	12077323
MGI:3820403	M	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm4Sho>/Y,Gata2<tm2Sho>/Gata2<tm2Sho>	involves: 129S6/SvEvTac * C57BL/6	N	12077323
MGI:3820403	M	MP:0000245	abnormal erythropoiesis	Gata1<tm4Sho>/Y,Gata2<tm2Sho>/Gata2<tm2Sho>	involves: 129S6/SvEvTac * C57BL/6	N	12077323
MGI:3820403	M	MP:0005397	hematopoietic system phenotype	Gata1<tm4Sho>/Y,Gata2<tm2Sho>/Gata2<tm2Sho>	involves: 129S6/SvEvTac * C57BL/6	Y	12077323
MGI:3820403	M	MP:0011091	prenatal lethality, complete penetrance	Gata1<tm4Sho>/Y,Gata2<tm2Sho>/Gata2<tm2Sho>	involves: 129S6/SvEvTac * C57BL/6	N	12077323
MGI:3820405	F	MP:0001127	small ovary	Sod1<tm1Leb>/Sod1<tm1Leb>	involves: 129S7/SvEvBrd * C57BL/6	N	9724058
MGI:3820405	F	MP:0002680	decreased corpora lutea number	Sod1<tm1Leb>/Sod1<tm1Leb>	involves: 129S7/SvEvBrd * C57BL/6	N	9724058
MGI:3820405	F	MP:0001926	female infertility	Sod1<tm1Leb>/Sod1<tm1Leb>	involves: 129S7/SvEvBrd * C57BL/6	N	9724058
MGI:3820405	F	MP:0001129	impaired ovarian folliculogenesis	Sod1<tm1Leb>/Sod1<tm1Leb>	involves: 129S7/SvEvBrd * C57BL/6	N	9724058
MGI:3820405	F	MP:0001923	reduced female fertility	Sod1<tm1Leb>/Sod1<tm1Leb>	involves: 129S7/SvEvBrd * C57BL/6	N	9724058
MGI:3820405	F	MP:0002682	decreased mature ovarian follicle number	Sod1<tm1Leb>/Sod1<tm1Leb>	involves: 129S7/SvEvBrd * C57BL/6	N	9724058
MGI:3820405	F	MP:0001126	abnormal ovary morphology	Sod1<tm1Leb>/Sod1<tm1Leb>	involves: 129S7/SvEvBrd * C57BL/6	N	9724058
MGI:3820408	M	MP:0000245	abnormal erythropoiesis	Gata1<tm5(GATA3)Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820408	M	MP:0003717	pallor	Gata1<tm5(GATA3)Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820408	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Gata1<tm5(GATA3)Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820408	M	MP:0000291	enlarged pericardium	Gata1<tm5(GATA3)Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820408	M	MP:0001698	decreased embryo size	Gata1<tm5(GATA3)Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820408	M	MP:0001722	pale yolk sac	Gata1<tm5(GATA3)Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820408	M	MP:0001577	anemia	Gata1<tm5(GATA3)Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820409	F	MP:0002875	decreased erythrocyte cell number	Gata1<tm5(GATA3)Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820409	F	MP:0001722	pale yolk sac	Gata1<tm5(GATA3)Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820409	F	MP:0002123	abnormal definitive hematopoiesis	Gata1<tm5(GATA3)Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820409	F	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance	Gata1<tm5(GATA3)Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820409	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Gata1<tm5(GATA3)Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820409	F	MP:0003717	pallor	Gata1<tm5(GATA3)Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820409	F	MP:0001577	anemia	Gata1<tm5(GATA3)Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820409	F	MP:0008770	decreased survivor rate	Gata1<tm5(GATA3)Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9576834
MGI:3820424	M	MP:0002675	asthenozoospermia	Spag6l<tm1Jfs>/Spag6l<+>	involves: 129X1/SvJ * C57BL/6J	N	12167721
MGI:3821573	F	MP:0004256	abnormal maternal decidual layer morphology	Smchd1<MommeD1>/Smchd1<MommeD1>	involves: C57BL/6 * FVB/N	N	18425126
MGI:3821610	M	MP:0002210	abnormal sex determination	Trim28<MommeD9>/Trim28<+>	involves: FVB/N	N	19099580
MGI:3821610	M	MP:0001935	decreased litter size	Trim28<MommeD9>/Trim28<+>	involves: FVB/N	N	19099580
MGI:3821716	F	MP:0001935	decreased litter size	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821716	F	MP:0011121	decreased primordial ovarian follicle number	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821716	F	MP:0031018	decreased granulosa cell proliferation	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821716	F	MP:0031420	decreased superovulation rate	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821716	F	MP:0031239	increased atretic ovarian follicle number	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821716	F	MP:0001129	impaired ovarian folliculogenesis	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821716	F	MP:0002682	decreased mature ovarian follicle number	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821716	F	MP:0001923	reduced female fertility	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821716	F	MP:0003077	abnormal cell cycle	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821716	F	MP:0004759	decreased mitotic index	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821716	F	MP:0031381	decreased secondary ovarian follicle number	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821716	F	MP:0005185	decreased circulating progesterone level	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821716	F	MP:0005182	increased circulating estradiol level	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821716	F	MP:0013508	increased granulosa cell apoptosis	Crybb2<tm1Itl>/Crybb2<tm1Itl>	C57BL/6-Crybb2<tm1Itl>	N	25245288
MGI:3821728	F	MP:0003845	abnormal decidualization	Dlgap5<tm1Tfts>/Dlgap5<tm1Tfts>	involves: 129S7/SvEvBrd	N	18676373
MGI:3821728	F	MP:0001926	female infertility	Dlgap5<tm1Tfts>/Dlgap5<tm1Tfts>	involves: 129S7/SvEvBrd	N	18676373
MGI:3822013	F	MP:0008779	abnormal maternal behavior	Dock7<mnlt>/Dock7<mnlt>	C57BL/6J-Dock7<mnlt>	N	19202056
MGI:3822028	F	MP:0002293	long gestation period	Bmp2<tm1Brd>/Bmp2<tm1Mis>	involves: 129S7/SvEvBrd * C57BL/6J	N	18769073
MGI:3822166	F	MP:0004047	abnormal milk composition	Ccr10<tm1Cge>/Ccr10<tm1Cge>	C.129S4-Ccr10<tm1Cge>	N	18941222
MGI:3822315	F	MP:0009021	absent estrus	Lepr<db>/Lepr<db>	involves: C57BL/6 * C57BLKS/J	N	20068132
MGI:3822315	F	MP:0001926	female infertility	Lepr<db>/Lepr<db>	involves: C57BL/6 * C57BLKS/J	N	20068132
MGI:3822315	F	MP:0001926	female infertility	Lepr<db>/Lepr<db>	involves: C57BL/6 * C57BLKS/J	N	19015522
MGI:3822315	F	MP:0001119	abnormal female reproductive system morphology	Lepr<db>/Lepr<db>	involves: C57BL/6 * C57BLKS/J	N	20068132
MGI:3822317	F	MP:0001926	female infertility	Lepr<tm1Yli>/Lepr<tm1Yli>	B6.129-Lepr<tm1Yli>	N	19015522
MGI:3822317	M	MP:0001925	male infertility	Lepr<tm1Yli>/Lepr<tm1Yli>	B6.129-Lepr<tm1Yli>	N	19015522
MGI:3822318	M	MP:0001925	male infertility	Lepr<tm2Yli>/Lepr<tm2Yli>	B6.129-Lepr<tm2Yli>	N	19015522
MGI:3822318	F	MP:0001923	reduced female fertility	Lepr<tm2Yli>/Lepr<tm2Yli>	B6.129-Lepr<tm2Yli>	N	19015522
MGI:3822371	F	MP:0009360	endometrium inflammation	Epha1<tm1Sld>/Epha1<tm1Sld>	involves: 129 * C57BL/6J	N	18802966
MGI:3822371	F	MP:0001926	female infertility	Epha1<tm1Sld>/Epha1<tm1Sld>	involves: 129 * C57BL/6J	N	18802966
MGI:3822371	F	MP:0009087	dilated uterine horn	Epha1<tm1Sld>/Epha1<tm1Sld>	involves: 129 * C57BL/6J	N	18802966
MGI:3822371	F	MP:0003537	hydrometrocolpos	Epha1<tm1Sld>/Epha1<tm1Sld>	involves: 129 * C57BL/6J	N	18802966
MGI:3822371	F	MP:0004906	enlarged uterus	Epha1<tm1Sld>/Epha1<tm1Sld>	involves: 129 * C57BL/6J	N	18802966
MGI:3822371	F	MP:0004904	increased uterus weight	Epha1<tm1Sld>/Epha1<tm1Sld>	involves: 129 * C57BL/6J	N	18802966
MGI:3822371	F	MP:0001144	vagina atresia	Epha1<tm1Sld>/Epha1<tm1Sld>	involves: 129 * C57BL/6J	N	18802966
MGI:3822485	F	MP:0009373	abnormal cumulus expansion	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad2<tm1Cxd>/Smad2<tm1.1Mwst>,Smad3<tm1Par>/Smad3<tm1Zuk>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	18809571
MGI:3822485	F	MP:0005431	decreased oocyte number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad2<tm1Cxd>/Smad2<tm1.1Mwst>,Smad3<tm1Par>/Smad3<tm1Zuk>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	18809571
MGI:3822485	F	MP:0031239	increased atretic ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad2<tm1Cxd>/Smad2<tm1.1Mwst>,Smad3<tm1Par>/Smad3<tm1Zuk>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	18809571
MGI:3822485	F	MP:0031020	premature ovarian failure	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad2<tm1Cxd>/Smad2<tm1.1Mwst>,Smad3<tm1Par>/Smad3<tm1Zuk>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	18809571
MGI:3822485	F	MP:0011129	decreased tertiary ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad2<tm1Cxd>/Smad2<tm1.1Mwst>,Smad3<tm1Par>/Smad3<tm1Zuk>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	18809571
MGI:3822485	F	MP:0001131	abnormal ovarian follicle morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad2<tm1Cxd>/Smad2<tm1.1Mwst>,Smad3<tm1Par>/Smad3<tm1Zuk>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	18809571
MGI:3822485	F	MP:0001923	reduced female fertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad2<tm1Cxd>/Smad2<tm1.1Mwst>,Smad3<tm1Par>/Smad3<tm1Zuk>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	18809571
MGI:3822520	M	MP:0001925	male infertility	hem6/hem6	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	N	18780836
MGI:3822520	M	MP:0002675	asthenozoospermia	hem6/hem6	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	N	18780836
MGI:3822520	M	MP:0005578	teratozoospermia	hem6/hem6	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	N	18780836
MGI:3822533	F	MP:0005431	decreased oocyte number	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	N	18805989
MGI:3822533	F	MP:0001928	abnormal ovulation	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	N	18805989
MGI:3822533	F	MP:0014445	abnormal spindle assembly in female meiosis	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	N	18805989
MGI:3822533	F	MP:0008871	abnormal ovarian follicle number	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	N	18805989
MGI:3822533	F	MP:0011121	decreased primordial ovarian follicle number	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	N	18805989
MGI:3822533	F	MP:0009648	abnormal superovulation	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	N	18805989
MGI:3822533	M	MP:0001925	male infertility	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	N	18805989
MGI:3822533	F	MP:0001926	female infertility	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	N	18805989
MGI:3822533	F	MP:0031422	failure of superovulation	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	N	18805989
MGI:3822734	F	MP:0001923	reduced female fertility	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	involves: 129P2/OlaHsd * C57BL/6 * ICR	N	12409213
MGI:3822734	F	MP:0009326	absent maternal crouching	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	involves: 129P2/OlaHsd * C57BL/6 * ICR	N	12409213
MGI:3822735	F	MP:0001923	reduced female fertility	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	B6.129-Adcyap1<tm1Nms>	N	17945412
MGI:3822735	F	MP:0002566	abnormal sexual interaction	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	B6.129-Adcyap1<tm1Nms>	N	17945412
MGI:3822735	F	MP:0001729	impaired embryo implantation	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	B6.129-Adcyap1<tm1Nms>	N	17945412
MGI:3822800	M	MP:0006378	abnormal spermatogonia morphology	Phyh<tm1Safe>/Phyh<tm1Safe>	involves: 129P2/OlaHsd * 129X1/SvJ * Black Swiss * FVB/N	N	19004801
MGI:3822903	F	MP:0012529	abnormal decidua basalis morphology	Il2rg<tm1Sug>/Il2rg<tm1Sug>	B6.129-Il2rg<tm1Sug>	N	12069389
MGI:3822903	F	MP:0005389	reproductive system phenotype	Il2rg<tm1Sug>/Il2rg<tm1Sug>	B6.129-Il2rg<tm1Sug>	Y	12069389
MGI:3822903	F	MP:0008047	absent uterine NK cells	Il2rg<tm1Sug>/Il2rg<tm1Sug>	B6.129-Il2rg<tm1Sug>	N	12069389
MGI:3822903	F	MP:0009020	prolonged metestrus	Il2rg<tm1Sug>/Il2rg<tm1Sug>	B6.129-Il2rg<tm1Sug>	N	12069389
MGI:3822903	F	MP:0009006	prolonged estrous cycle	Il2rg<tm1Sug>/Il2rg<tm1Sug>	B6.129-Il2rg<tm1Sug>	N	12069389
MGI:3822903	F	MP:0004256	abnormal maternal decidual layer morphology	Il2rg<tm1Sug>/Il2rg<tm1Sug>	B6.129-Il2rg<tm1Sug>	N	12069389
MGI:3822903	F	MP:0009011	prolonged diestrus	Il2rg<tm1Sug>/Il2rg<tm1Sug>	B6.129-Il2rg<tm1Sug>	N	12069389
MGI:3822903	F	MP:0001927	abnormal estrous cycle	Il2rg<tm1Sug>/Il2rg<tm1Sug>	B6.129-Il2rg<tm1Sug>	N	12069389
MGI:3822903	F	MP:0010776	abnormal placenta metrial gland morphology	Il2rg<tm1Sug>/Il2rg<tm1Sug>	B6.129-Il2rg<tm1Sug>	N	12069389
MGI:3822904	M	MP:0009232	abnormal sperm nucleus morphology	Aurkc<tm1Lex>/Aurkc<tm1Lex>	B6.129S-Aurkc<tm1Lex>	N	17192404
MGI:3822904	M	MP:0008898	abnormal acrosome morphology	Aurkc<tm1Lex>/Aurkc<tm1Lex>	B6.129S-Aurkc<tm1Lex>	N	17192404
MGI:3822904	M	MP:0009231	detached acrosome	Aurkc<tm1Lex>/Aurkc<tm1Lex>	B6.129S-Aurkc<tm1Lex>	N	17192404
MGI:3822904	M	MP:0009230	abnormal sperm head morphology	Aurkc<tm1Lex>/Aurkc<tm1Lex>	B6.129S-Aurkc<tm1Lex>	N	17192404
MGI:3822906	M	MP:0001922	reduced male fertility	Tg(B4galt1-Aurkb*K111R*L323I)1Saco/0	involves: 129/Sv * C57BL/6J * SJL	N	17192404
MGI:3822906	M	MP:0005169	abnormal male meiosis	Tg(B4galt1-Aurkb*K111R*L323I)1Saco/0	involves: 129/Sv * C57BL/6J * SJL	N	17192404
MGI:3822906	M	MP:0006380	abnormal spermatid morphology	Tg(B4galt1-Aurkb*K111R*L323I)1Saco/0	involves: 129/Sv * C57BL/6J * SJL	N	17192404
MGI:3822906	M	MP:0002687	oligozoospermia	Tg(B4galt1-Aurkb*K111R*L323I)1Saco/0	involves: 129/Sv * C57BL/6J * SJL	N	17192404
MGI:3822906	M	MP:0001156	abnormal spermatogenesis	Tg(B4galt1-Aurkb*K111R*L323I)1Saco/0	involves: 129/Sv * C57BL/6J * SJL	N	17192404
MGI:3822914	M	MP:0004851	increased testis weight	Slc14a1<tm1Ask>/Slc14a1<tm1Ask>	involves: C57BL/6J * CD-1	N	17475664
MGI:3822914	M	MP:0003830	abnormal testis development	Slc14a1<tm1Ask>/Slc14a1<tm1Ask>	involves: C57BL/6J * CD-1	N	17475664
MGI:3822914	M	MP:0004109	abnormal Sertoli cell development	Slc14a1<tm1Ask>/Slc14a1<tm1Ask>	involves: C57BL/6J * CD-1	N	17475664
MGI:3822914	M	MP:0001156	abnormal spermatogenesis	Slc14a1<tm1Ask>/Slc14a1<tm1Ask>	involves: C57BL/6J * CD-1	N	17475664
MGI:3822914	M	MP:0004884	abnormal testis physiology	Slc14a1<tm1Ask>/Slc14a1<tm1Ask>	involves: C57BL/6J * CD-1	N	17475664
MGI:3822916	M	MP:0006418	abnormal testis cord formation	Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822916	M	MP:0001156	abnormal spermatogenesis	Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822916	M	MP:0006379	abnormal spermatocyte morphology	Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822916	M	MP:0001146	abnormal testis morphology	Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822916	M	MP:0001147	small testis	Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822916	M	MP:0005536	decreased Leydig cell number	Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822916	M	MP:0001925	male infertility	Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822917	F	MP:0001926	female infertility	Pdgfra<tm1Sor>/Pdgfra<+>,Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822917	F	MP:0009370	decreased theca cell number	Pdgfra<tm1Sor>/Pdgfra<+>,Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822917	F	MP:0001121	uterus hypoplasia	Pdgfra<tm1Sor>/Pdgfra<+>,Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822917	F	MP:0008869	anovulation	Pdgfra<tm1Sor>/Pdgfra<+>,Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822917	F	MP:0001127	small ovary	Pdgfra<tm1Sor>/Pdgfra<+>,Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822917	M	MP:0001925	male infertility	Pdgfra<tm1Sor>/Pdgfra<+>,Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822917	F	MP:0001126	abnormal ovary morphology	Pdgfra<tm1Sor>/Pdgfra<+>,Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822917	F	MP:0001134	absent corpus luteum	Pdgfra<tm1Sor>/Pdgfra<+>,Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822917	F	MP:0011129	decreased tertiary ovarian follicle number	Pdgfra<tm1Sor>/Pdgfra<+>,Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822996	M	MP:0001925	male infertility	Pdgfrb<tm1Sor>/Pdgfrb<+>,Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>	either: (involves: 129S4/SvJaeSor * 129S7/SvEvBrd) or (involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6)	N	19056881
MGI:3822998	F	MP:0004906	enlarged uterus	Tiparp<Gt(ROSA)79Sor>/Tiparp<Gt(ROSA)79Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822998	F	MP:0011128	increased tertiary ovarian follicle number	Tiparp<Gt(ROSA)79Sor>/Tiparp<Gt(ROSA)79Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822998	F	MP:0002293	long gestation period	Tiparp<Gt(ROSA)79Sor>/Tiparp<Gt(ROSA)79Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822998	F	MP:0002016	ovary cyst	Tiparp<Gt(ROSA)79Sor>/Tiparp<Gt(ROSA)79Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822998	F	MP:0002681	increased corpora lutea number	Tiparp<Gt(ROSA)79Sor>/Tiparp<Gt(ROSA)79Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822998	F	MP:0001923	reduced female fertility	Tiparp<Gt(ROSA)79Sor>/Tiparp<Gt(ROSA)79Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822998	F	MP:0004832	enlarged ovary	Tiparp<Gt(ROSA)79Sor>/Tiparp<Gt(ROSA)79Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3822998	F	MP:0009006	prolonged estrous cycle	Tiparp<Gt(ROSA)79Sor>/Tiparp<Gt(ROSA)79Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823001	F	MP:0001926	female infertility	Pdgfra<tm1Sor>/Pdgfra<+>,Tiparp<Gt(ROSA)79Sor>/Tiparp<Gt(ROSA)79Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823002	F	MP:0001926	female infertility	Pdgfrb<tm1Sor>/Pdgfrb<+>,Tiparp<Gt(ROSA)79Sor>/Tiparp<Gt(ROSA)79Sor>	either: (involves: 129S4/SvJaeSor * 129S7/SvEvBrd) or (involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6)	N	19056881
MGI:3823005	F	MP:0001134	absent corpus luteum	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	F	MP:0008869	anovulation	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	M	MP:0001925	male infertility	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	M	MP:0020550	multinucleated giant male germ cells	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	M	MP:0006379	abnormal spermatocyte morphology	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	F	MP:0001926	female infertility	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	M	MP:0001147	small testis	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	M	MP:0006418	abnormal testis cord formation	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	F	MP:0009370	decreased theca cell number	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	F	MP:0001121	uterus hypoplasia	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	F	MP:0001126	abnormal ovary morphology	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	F	MP:0001127	small ovary	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	M	MP:0006380	abnormal spermatid morphology	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	M	MP:0005536	decreased Leydig cell number	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	F	MP:0011129	decreased tertiary ovarian follicle number	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	M	MP:0001146	abnormal testis morphology	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823005	M	MP:0001156	abnormal spermatogenesis	Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823017	F	MP:0001926	female infertility	Pdgfra<tm1Sor>/Pdgfra<+>,Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823017	M	MP:0001925	male infertility	Pdgfra<tm1Sor>/Pdgfra<+>,Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823018	M	MP:0001925	male infertility	Pdgfrb<tm1Sor>/Pdgfrb<+>,Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor * 129S7/SvEvBrd) or (involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6)	N	19056881
MGI:3823018	F	MP:0001926	female infertility	Pdgfrb<tm1Sor>/Pdgfrb<+>,Sgpl1<Gt(ROSA)78Sor>/Sgpl1<Gt(ROSA)78Sor>	either: (involves: 129S4/SvJaeSor * 129S7/SvEvBrd) or (involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6)	N	19056881
MGI:3823020	F	MP:0001127	small ovary	Pdgfra<tm1Sor>/Pdgfra<+>,Schip1<Gt(ROSA)77Sor>/Schip1<Gt(ROSA)77Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823020	F	MP:0001126	abnormal ovary morphology	Pdgfra<tm1Sor>/Pdgfra<+>,Schip1<Gt(ROSA)77Sor>/Schip1<Gt(ROSA)77Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823020	F	MP:0008869	anovulation	Pdgfra<tm1Sor>/Pdgfra<+>,Schip1<Gt(ROSA)77Sor>/Schip1<Gt(ROSA)77Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823020	F	MP:0001926	female infertility	Pdgfra<tm1Sor>/Pdgfra<+>,Schip1<Gt(ROSA)77Sor>/Schip1<Gt(ROSA)77Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823020	F	MP:0002680	decreased corpora lutea number	Pdgfra<tm1Sor>/Pdgfra<+>,Schip1<Gt(ROSA)77Sor>/Schip1<Gt(ROSA)77Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823020	F	MP:0009370	decreased theca cell number	Pdgfra<tm1Sor>/Pdgfra<+>,Schip1<Gt(ROSA)77Sor>/Schip1<Gt(ROSA)77Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823020	F	MP:0001121	uterus hypoplasia	Pdgfra<tm1Sor>/Pdgfra<+>,Schip1<Gt(ROSA)77Sor>/Schip1<Gt(ROSA)77Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823020	F	MP:0011129	decreased tertiary ovarian follicle number	Pdgfra<tm1Sor>/Pdgfra<+>,Schip1<Gt(ROSA)77Sor>/Schip1<Gt(ROSA)77Sor>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823024	F	MP:0001127	small ovary	2610005L07Rik<Gt(ROSA)73Sor>/2610005L07Rik<Gt(ROSA)73Sor>,Pdgfra<tm1Sor>/Pdgfra<+>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823024	F	MP:0008869	anovulation	2610005L07Rik<Gt(ROSA)73Sor>/2610005L07Rik<Gt(ROSA)73Sor>,Pdgfra<tm1Sor>/Pdgfra<+>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823024	F	MP:0011129	decreased tertiary ovarian follicle number	2610005L07Rik<Gt(ROSA)73Sor>/2610005L07Rik<Gt(ROSA)73Sor>,Pdgfra<tm1Sor>/Pdgfra<+>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823024	F	MP:0001926	female infertility	2610005L07Rik<Gt(ROSA)73Sor>/2610005L07Rik<Gt(ROSA)73Sor>,Pdgfra<tm1Sor>/Pdgfra<+>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823024	F	MP:0002680	decreased corpora lutea number	2610005L07Rik<Gt(ROSA)73Sor>/2610005L07Rik<Gt(ROSA)73Sor>,Pdgfra<tm1Sor>/Pdgfra<+>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823024	F	MP:0001126	abnormal ovary morphology	2610005L07Rik<Gt(ROSA)73Sor>/2610005L07Rik<Gt(ROSA)73Sor>,Pdgfra<tm1Sor>/Pdgfra<+>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823024	F	MP:0009370	decreased theca cell number	2610005L07Rik<Gt(ROSA)73Sor>/2610005L07Rik<Gt(ROSA)73Sor>,Pdgfra<tm1Sor>/Pdgfra<+>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823024	F	MP:0001121	uterus hypoplasia	2610005L07Rik<Gt(ROSA)73Sor>/2610005L07Rik<Gt(ROSA)73Sor>,Pdgfra<tm1Sor>/Pdgfra<+>	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823036	M	MP:0006379	abnormal spermatocyte morphology	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823036	M	MP:0006418	abnormal testis cord formation	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823036	F	MP:0001121	uterus hypoplasia	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823036	F	MP:0001131	abnormal ovarian follicle morphology	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823036	M	MP:0002687	oligozoospermia	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823036	F	MP:0009370	decreased theca cell number	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823036	M	MP:0005536	decreased Leydig cell number	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823036	M	MP:0001146	abnormal testis morphology	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823036	M	MP:0001147	small testis	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823036	F	MP:0001127	small ovary	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823036	F	MP:0008869	anovulation	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823039	M	MP:0001147	small testis	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Pdgfrb<tm11Sor>/Pdgfrb<tm11Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823039	M	MP:0031138	testicular hemorrhage	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Pdgfrb<tm11Sor>/Pdgfrb<tm11Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823039	M	MP:0001146	abnormal testis morphology	Pdgfra<tm8Sor>/Pdgfra<tm8Sor>,Pdgfrb<tm11Sor>/Pdgfrb<tm11Sor>,Tg(Nr5a1-cre)2Klp/0	either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)	N	19056881
MGI:3823069	M	MP:0008489	slow postnatal weight gain	Htr2c<tm1Knk>/Y	C.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823070	F	MP:0008489	slow postnatal weight gain	Htr2c<tm1Knk>/Htr2c<tm1Knk>	C.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823071	F	MP:0001262	decreased body weight	Htr2c<tm1Knk>/Htr2c<tm1Knk>	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823071	F	MP:0001258	decreased body length	Htr2c<tm1Knk>/Htr2c<tm1Knk>	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823071	F	MP:0008489	slow postnatal weight gain	Htr2c<tm1Knk>/Htr2c<tm1Knk>	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823071	F	MP:0011086	postnatal lethality, incomplete penetrance	Htr2c<tm1Knk>/Htr2c<tm1Knk>	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823071	F	MP:0006086	decreased body mass index	Htr2c<tm1Knk>/Htr2c<tm1Knk>	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0002727	decreased circulating insulin level	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0005376	homeostasis/metabolism phenotype	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	Y	19036977
MGI:3823072	M	MP:0001258	decreased body length	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0004701	decreased circulating insulin-like growth factor I level	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0005179	decreased circulating cholesterol level	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0001783	decreased white adipose tissue amount	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0008965	increased basal metabolism	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0014143	decreased body fat mass	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0014169	decreased brown adipose tissue mass	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0005123	increased circulating growth hormone level	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0002644	decreased circulating triglyceride level	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0005560	decreased circulating glucose level	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0009746	enhanced behavioral response to xenobiotic	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0005535	abnormal body temperature	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0011612	increased circulating ghrelin level	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0008489	slow postnatal weight gain	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0005266	abnormal metabolism	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0011086	postnatal lethality, incomplete penetrance	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0001262	decreased body weight	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0001402	decreased locomotor activity	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0008873	increased physiological sensitivity to xenobiotic	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0005668	decreased circulating leptin level	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0001433	polyphagia	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0001732	postnatal growth retardation	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823072	M	MP:0006086	decreased body mass index	Htr2c<tm1Knk>/Y	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823073	M	MP:0006086	decreased body mass index	Htr2c<tm1Knk>/Y,Mc4r<tm1Lowl>/Mc4r<tm1Lowl>	involves: 129S4/SvJae * C57BL/6	N	19036977
MGI:3823073	M	MP:0005378	growth/size/body region phenotype	Htr2c<tm1Knk>/Y,Mc4r<tm1Lowl>/Mc4r<tm1Lowl>	involves: 129S4/SvJae * C57BL/6	Y	19036977
MGI:3823073	M	MP:0001433	polyphagia	Htr2c<tm1Knk>/Y,Mc4r<tm1Lowl>/Mc4r<tm1Lowl>	involves: 129S4/SvJae * C57BL/6	N	19036977
MGI:3823074	F	MP:0005378	growth/size/body region phenotype	Htr2c<tm2Knk>/Htr2c<tm2Knk>	either: B6.Cg-Htr2c<tm2Knk> or C.Cg-Htr2c<tm2Knk>	Y	19036977
MGI:3823074	F	MP:0005376	homeostasis/metabolism phenotype	Htr2c<tm2Knk>/Htr2c<tm2Knk>	either: B6.Cg-Htr2c<tm2Knk> or C.Cg-Htr2c<tm2Knk>	Y	19036977
MGI:3823075	M	MP:0005378	growth/size/body region phenotype	Htr2c<tm2Knk>/Y	either: B6.Cg-Htr2c<tm2Knk> or C.Cg-Htr2c<tm2Knk>	Y	19036977
MGI:3823075	M	MP:0005376	homeostasis/metabolism phenotype	Htr2c<tm2Knk>/Y	either: B6.Cg-Htr2c<tm2Knk> or C.Cg-Htr2c<tm2Knk>	Y	19036977
MGI:3823076	F	MP:0008489	slow postnatal weight gain	Htr2c<tm1Knk>/Htr2c<+>	B6.Cg-Htr2c<tm1Knk>	N	19036977
MGI:3823077	F	MP:0008489	slow postnatal weight gain	Htr2c<tm1Knk>/Htr2c<tm2Knk>	B6.Cg-Htr2c<tm1Knk>/Htr2c<tm2Knk>	N	19036977
MGI:3826391	F	MP:0001926	female infertility	Oca2<p-12DTR>/Oca2<p-12DTR>	involves: 101/Rl * C3H/Rl	N	8601493
MGI:3826391	M	MP:0001925	male infertility	Oca2<p-12DTR>/Oca2<p-12DTR>	involves: 101/Rl * C3H/Rl	N	8601493
MGI:3826409	F	MP:0003675	kidney cyst	Gpc3<Gt(Ex136)Byg>/Gpc3<Gt(Ex136)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	11431694
MGI:3826409	F	MP:0011087	neonatal lethality, complete penetrance	Gpc3<Gt(Ex136)Byg>/Gpc3<Gt(Ex136)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	11431694
MGI:3826409	F	MP:0001699	increased embryo size	Gpc3<Gt(Ex136)Byg>/Gpc3<Gt(Ex136)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	11431694
MGI:3826446	F	MP:0001926	female infertility	Foxo3<tm1Nmt>/Foxo3<tm1Nmt>	involves: C57BL/6	N	18371339
MGI:3826833	M	MP:0002166	abnormal tumor susceptibility	Rag1<tm1Mom>/Rag1<tm1Mom>,Tyrp1<B-w>/Tyrp1<B-w>,X/Tg(Tcra,Tcrb)9Rest	involves: 101/Rl * 129S7/SvEvBrd * C3H/Rl * C57BL/6	N	18354038
MGI:3826965	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Hccs<tm1Tcc>/Hccs<tm1Tcc>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826966	M	MP:0008788	abnormal fetal cardiomyocyte morphology	Hccs<tm1Tcc>/Y,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826966	M	MP:0031607	abnormal fetal cardiomyocyte mitochondrial morphology	Hccs<tm1Tcc>/Y,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826966	M	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Hccs<tm1Tcc>/Y,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826966	M	MP:0010955	abnormal respiratory electron transport chain	Hccs<tm1Tcc>/Y,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826966	M	MP:0014072	decreased cardiac muscle glycogen level	Hccs<tm1Tcc>/Y,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826966	M	MP:0011395	decreased fetal cardiomyocyte proliferation	Hccs<tm1Tcc>/Y,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0010955	abnormal respiratory electron transport chain	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0002953	thick ventricular wall	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0004215	abnormal myocardial fiber physiology	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0000274	enlarged heart	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0005608	cardiac interstitial fibrosis	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0010520	sinoatrial block	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0002083	premature death	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0005329	abnormal myocardium layer morphology	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0001855	abnormal atrial thrombosis	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0002753	dilated heart left ventricle	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0031607	abnormal fetal cardiomyocyte mitochondrial morphology	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0002754	dilated heart right ventricle	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0010636	bundle branch block	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0010519	atrioventricular block	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0003140	dilated heart atrium	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826967	F	MP:0002795	dilated cardiomyopathy	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>	involves: 129S1/Sv	N	18854137
MGI:3826982	F	MP:0008788	abnormal fetal cardiomyocyte morphology	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>,Tg(CAG-EGFP)D4Nagy/0,Tg(Hmgcr-lacZ)H253Sest/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	18854137
MGI:3826982	F	MP:0003567	abnormal fetal cardiomyocyte proliferation	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>,Tg(CAG-EGFP)D4Nagy/0,Tg(Hmgcr-lacZ)H253Sest/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	18854137
MGI:3826982	F	MP:0031608	decreased fetal cardiomyocyte size	Hccs<tm1Tcc>/Hccs<+>,Nkx2-5<tm2(cre)Rph>/Nkx2-5<+>,Tg(CAG-EGFP)D4Nagy/0,Tg(Hmgcr-lacZ)H253Sest/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	18854137
MGI:3828308	M	MP:0001405	impaired coordination	Plp1<tm1Frca>/Y	B6.129-Plp1<tm1Frca>	N	18835559
MGI:3828308	M	MP:0005405	axon degeneration	Plp1<tm1Frca>/Y	B6.129-Plp1<tm1Frca>	N	18835559
MGI:3828308	M	MP:0005386	behavior/neurological phenotype	Plp1<tm1Frca>/Y	B6.129-Plp1<tm1Frca>	Y	18835559
MGI:3828308	M	MP:0000921	demyelination	Plp1<tm1Frca>/Y	B6.129-Plp1<tm1Frca>	N	18835559
MGI:3828308	M	MP:0003871	abnormal myelin sheath morphology	Plp1<tm1Frca>/Y	B6.129-Plp1<tm1Frca>	N	18835559
MGI:3828332	M	MP:0001925	male infertility	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	N	MGI:1349786
MGI:3828332	F	MP:0002680	decreased corpora lutea number	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	N	MGI:1349786
MGI:3828332	F	MP:0001923	reduced female fertility	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	N	MGI:1349786
MGI:3828332	M	MP:0004901	decreased male germ cell number	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	N	MGI:1349786
MGI:3828332	M	MP:0006380	abnormal spermatid morphology	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	N	MGI:1349786
MGI:3828332	M	MP:0002687	oligozoospermia	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	N	MGI:1349786
MGI:3828986	F	MP:0002196	absent corpus callosum	Ccrs3<BTBR T-+- Itpr3-tf/J>/Ccrs3<BTBR T-+- Itpr3-tf/J>	involves: BALB/cBy * BTBR T<+> Itpr3<tf>/J	N	16899052
MGI:3828989	F	MP:0002196	absent corpus callosum	Ccrs3<BALB/cByJ>/Ccrs3<BTBR T-+- Itpr3-tf/J>	involves: BALB/cBy * BTBR T<+> Itpr3<tf>/J	N	16899052
MGI:3828990	F	MP:0002196	absent corpus callosum	Ccrs4<BTBR T-+- Itpr3-tf/J>/Ccrs4<BTBR T-+- Itpr3-tf/J>	involves: BALB/cBy * BTBR T<+> Itpr3<tf>/J	N	16899052
MGI:3828992	F	MP:0002196	absent corpus callosum	Ccrs4<BALB/cByJ>/Ccrs4<BTBR T-+- Itpr3-tf/J>	involves: BALB/cBy * BTBR T<+> Itpr3<tf>/J	N	16899052
MGI:3829008	F	MP:0001923	reduced female fertility	Tmprss6<m3Btlr>/Tmprss6<m3Btlr>	C57BL/6J-Tmprss6<m3Btlr>	N	MGI:3829006
MGI:3829188	M	MP:0004542	impaired acrosome reaction	Prss21<tm1Tba>/Prss21<tm1Tba>	involves: 129S2/SvPas * ICR	N	18754795
MGI:3829188	M	MP:0030976	impaired sperm penetration of zona pellucida	Prss21<tm1Tba>/Prss21<tm1Tba>	involves: 129S2/SvPas * ICR	N	18754795
MGI:3829188	M	MP:0030978	impaired binding of sperm to zona pellucida	Prss21<tm1Tba>/Prss21<tm1Tba>	involves: 129S2/SvPas * ICR	N	18754795
MGI:3829203	M	MP:0003120	abnormal tracheal cartilage morphology	Efnb1<tm1.1Sor>/Y,Efnb2<tm2Sor>/Efnb2<+>	involves: 129S4/SvJaeSor * C57BL/6J	N	17223098
MGI:3829203	M	MP:0009264	failure of eyelid fusion	Efnb1<tm1.1Sor>/Y,Efnb2<tm2Sor>/Efnb2<+>	involves: 129S4/SvJaeSor * C57BL/6J	N	17223098
MGI:3829203	M	MP:0000618	small salivary gland	Efnb1<tm1.1Sor>/Y,Efnb2<tm2Sor>/Efnb2<+>	involves: 129S4/SvJaeSor * C57BL/6J	N	17223098
MGI:3829204	F	MP:0003120	abnormal tracheal cartilage morphology	Efnb1<tm1.1Sor>/Efnb1<+>,Efnb2<tm2Sor>/Efnb2<+>	involves: 129S4/SvJaeSor * C57BL/6J	N	17223098
MGI:3829204	F	MP:0000618	small salivary gland	Efnb1<tm1.1Sor>/Efnb1<+>,Efnb2<tm2Sor>/Efnb2<+>	involves: 129S4/SvJaeSor * C57BL/6J	N	17223098
MGI:3829204	F	MP:0009264	failure of eyelid fusion	Efnb1<tm1.1Sor>/Efnb1<+>,Efnb2<tm2Sor>/Efnb2<+>	involves: 129S4/SvJaeSor * C57BL/6J	N	17223098
MGI:3829421	F	MP:0002435	abnormal effector T cell morphology	Foxp3<sf>/Foxp3<sf>,Tg(Rorc-EGFP)1Ebe/?	involves: C57BL/6	N	18504307
MGI:3829438	F	MP:0009092	endometrium hyperplasia	Pten<tm2Mak>/Pten<tm2Mak>,Tg(Cyp1a1-cre)1Dwi/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	19011632
MGI:3829439	F	MP:0001134	absent corpus luteum	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	18758446
MGI:3829439	F	MP:0009081	thin uterus	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	18758446
MGI:3829439	M	MP:0001925	male infertility	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	18758446
MGI:3829439	F	MP:0001926	female infertility	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	18758446
MGI:3829605	F	MP:0004833	ovary atrophy	Sohlh2<tm1Miya>/Sohlh2<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19014927
MGI:3829605	F	MP:0001129	impaired ovarian folliculogenesis	Sohlh2<tm1Miya>/Sohlh2<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19014927
MGI:3829605	F	MP:0001931	abnormal oogenesis	Sohlh2<tm1Miya>/Sohlh2<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19014927
MGI:3829605	M	MP:0003205	testicular atrophy	Sohlh2<tm1Miya>/Sohlh2<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19014927
MGI:3829605	M	MP:0006378	abnormal spermatogonia morphology	Sohlh2<tm1Miya>/Sohlh2<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19014927
MGI:3829605	F	MP:0002777	absent ovarian follicles	Sohlh2<tm1Miya>/Sohlh2<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19014927
MGI:3829605	M	MP:0001925	male infertility	Sohlh2<tm1Miya>/Sohlh2<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19014927
MGI:3829605	F	MP:0001926	female infertility	Sohlh2<tm1Miya>/Sohlh2<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19014927
MGI:3829605	M	MP:0006379	abnormal spermatocyte morphology	Sohlh2<tm1Miya>/Sohlh2<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19014927
MGI:3829657	F	MP:0011101	prenatal lethality, incomplete penetrance	Xist<tm5Sado>/Xist<+>	involves: 129S4/SvJae	N	19036803
MGI:3829657	F	MP:0003787	abnormal imprinting	Xist<tm5Sado>/Xist<+>	involves: 129S4/SvJae	N	19036803
MGI:3829657	F	MP:0001672	abnormal embryo development	Xist<tm5Sado>/Xist<+>	involves: 129S4/SvJae	N	19036803
MGI:3829657	F	MP:0010736	abnormal extraembryonic ectoderm morphology	Xist<tm5Sado>/Xist<+>	involves: 129S4/SvJae	N	19036803
MGI:3829657	F	MP:0001698	decreased embryo size	Xist<tm5Sado>/Xist<+>	involves: 129S4/SvJae	N	19036803
MGI:3829712	F	MP:0002412	increased susceptibility to bacterial infection	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>,Rag2<tm1Fwa>/Rag2<tm1Fwa>	involves: 129P2/OlaHsd * 129S/SvEv	N	19084435
MGI:3829712	F	MP:0008568	abnormal interleukin secretion	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>,Rag2<tm1Fwa>/Rag2<tm1Fwa>	involves: 129P2/OlaHsd * 129S/SvEv	N	19084435
MGI:3829712	F	MP:0008045	decreased NK cell number	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>,Rag2<tm1Fwa>/Rag2<tm1Fwa>	involves: 129P2/OlaHsd * 129S/SvEv	N	19084435
MGI:3829752	F	MP:0001923	reduced female fertility	Rptor<tm1Rueg>/Rptor<tm1Rueg>,Tg(Fabp4-cre)1Rev/0	involves: 129S1/SvImJ * C57BL/6J	N	19046571
MGI:3829884	M	MP:0009230	abnormal sperm head morphology	Abshq1<PWK/PhJ>/Abshq1<PWK/PhJ>	involves: LEWES/EiJ * PWK/PhJ	N	18689897
MGI:3829885	M	MP:0009230	abnormal sperm head morphology	Abshq2<PWK/PhJ>/Abshq2<PWK/PhJ>	involves: LEWES/EiJ * PWK/PhJ	N	18689897
MGI:3829886	M	MP:0009230	abnormal sperm head morphology	Abshq3<PWK/PhJ>/Abshq3<PWK/PhJ>	involves: LEWES/EiJ * PWK/PhJ	N	18689897
MGI:3829894	M	MP:0009230	abnormal sperm head morphology	Abshq4<PWK/PhJ>/Abshq4<PWK/PhJ>	involves: LEWES/EiJ * PWK/PhJ	N	18689897
MGI:3829902	M	MP:0009230	abnormal sperm head morphology	Abshq5<PWK/PhJ>/Abshq5<PWK/PhJ>	involves: LEWES/EiJ * PWK/PhJ	N	18689897
MGI:3829903	M	MP:0009230	abnormal sperm head morphology	Abshq6<PWK/PhJ>/Abshq6<PWK/PhJ>	involves: LEWES/EiJ * PWK/PhJ	N	18689897
MGI:3829908	M	MP:0009230	abnormal sperm head morphology	Abshq7<PWK/PhJ>/Abshq7<PWK/PhJ>	involves: LEWES/EiJ * PWK/PhJ	N	18689897
MGI:3829917	M	MP:0004852	decreased testis weight	Rtwq1<PWK/PhJ>/Rtwq1<PWK/PhJ>	involves: LEWES/EiJ * PWK/PhJ	N	18689897
MGI:3829920	M	MP:0004852	decreased testis weight	Rtwq2<PWK/PhJ>/Rtwq2<PWK/PhJ>	involves: LEWES/EiJ * PWK/PhJ	N	18689897
MGI:3829931	M	MP:0002687	oligozoospermia	Lspcq1<PWK/PhJ>/Lspcq1<PWK/PhJ>	involves: LEWES/EiJ * PWK/PhJ	N	18689897
MGI:3830664	M	MP:0009231	detached acrosome	Rimbp3<tm1Gxu>/Rimbp3<tm1Gxu>	involves: 129/Sv * ICR	N	19091768
MGI:3830664	M	MP:0009232	abnormal sperm nucleus morphology	Rimbp3<tm1Gxu>/Rimbp3<tm1Gxu>	involves: 129/Sv * ICR	N	19091768
MGI:3830664	M	MP:0009377	ectopic manchette	Rimbp3<tm1Gxu>/Rimbp3<tm1Gxu>	involves: 129/Sv * ICR	N	19091768
MGI:3830664	M	MP:0009237	kinked sperm flagellum	Rimbp3<tm1Gxu>/Rimbp3<tm1Gxu>	involves: 129/Sv * ICR	N	19091768
MGI:3830664	M	MP:0001932	abnormal spermiogenesis	Rimbp3<tm1Gxu>/Rimbp3<tm1Gxu>	involves: 129/Sv * ICR	N	19091768
MGI:3830664	M	MP:0008893	detached sperm flagellum	Rimbp3<tm1Gxu>/Rimbp3<tm1Gxu>	involves: 129/Sv * ICR	N	19091768
MGI:3830664	M	MP:0002687	oligozoospermia	Rimbp3<tm1Gxu>/Rimbp3<tm1Gxu>	involves: 129/Sv * ICR	N	19091768
MGI:3830664	M	MP:0001925	male infertility	Rimbp3<tm1Gxu>/Rimbp3<tm1Gxu>	involves: 129/Sv * ICR	N	19091768
MGI:3830664	M	MP:0006380	abnormal spermatid morphology	Rimbp3<tm1Gxu>/Rimbp3<tm1Gxu>	involves: 129/Sv * ICR	N	19091768
MGI:3830664	M	MP:0009230	abnormal sperm head morphology	Rimbp3<tm1Gxu>/Rimbp3<tm1Gxu>	involves: 129/Sv * ICR	N	19091768
MGI:3830716	M	MP:0013624	decreased femur compact bone thickness	Bmd5a<C3H/HeJ>/Bmd5a<C3H/HeJ>	involves: C3H/HeJ * C57BL/6J	N	17451375
MGI:3830716	M	MP:0020010	decreased bone mineral density of femur	Bmd5a<C3H/HeJ>/Bmd5a<C3H/HeJ>	involves: C3H/HeJ * C57BL/6J	N	17451375
MGI:3830716	F	MP:0010875	increased bone volume	Bmd5a<C3H/HeJ>/Bmd5a<C3H/HeJ>	involves: C3H/HeJ * C57BL/6J	N	17451375
MGI:3830716	F	MP:0020011	increased bone mineral density of femur	Bmd5a<C3H/HeJ>/Bmd5a<C3H/HeJ>	involves: C3H/HeJ * C57BL/6J	N	17451375
MGI:3830716	F	MP:0013623	increased femur compact bone thickness	Bmd5a<C3H/HeJ>/Bmd5a<C3H/HeJ>	involves: C3H/HeJ * C57BL/6J	N	17451375
MGI:3830719	M	MP:0010875	increased bone volume	Bmd5b<C3H/HeJ>/Bmd5b<C3H/HeJ>	involves: C3H/HeJ * C57BL/6J	N	17451375
MGI:3831191	M	MP:0009199	abnormal external male genitalia morphology	Gprc6a<tm1Ldq>/Gprc6a<tm1Ldq>	involves: 129X1/SvJ * C57BL/6	N	19050760
MGI:3831191	M	MP:0004910	decreased seminal vesicle weight	Gprc6a<tm1Ldq>/Gprc6a<tm1Ldq>	involves: 129X1/SvJ * C57BL/6	N	19050760
MGI:3831191	M	MP:0000628	abnormal mammary gland development	Gprc6a<tm1Ldq>/Gprc6a<tm1Ldq>	involves: 129X1/SvJ * C57BL/6	N	19050760
MGI:3831191	M	MP:0009205	abnormal internal male genitalia morphology	Gprc6a<tm1Ldq>/Gprc6a<tm1Ldq>	involves: 129X1/SvJ * C57BL/6	N	19050760
MGI:3831191	M	MP:0001147	small testis	Gprc6a<tm1Ldq>/Gprc6a<tm1Ldq>	involves: 129X1/SvJ * C57BL/6	N	19050760
MGI:3831191	M	MP:0004852	decreased testis weight	Gprc6a<tm1Ldq>/Gprc6a<tm1Ldq>	involves: 129X1/SvJ * C57BL/6	N	19050760
MGI:3831195	M	MP:0001168	abnormal prostate gland epithelium morphology	Tg(Pbsn-Ar*E231G)7353Ng/0	involves: FVB/N	N	15657128
MGI:3831195	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(Pbsn-Ar*E231G)7353Ng/0	involves: FVB/N	N	15657128
MGI:3831195	M	MP:0010357	increased prostate gland tumor incidence	Tg(Pbsn-Ar*E231G)7353Ng/0	involves: FVB/N	N	15657128
MGI:3831195	M	MP:0009380	abnormal prostate gland ventral lobe morphology	Tg(Pbsn-Ar*E231G)7353Ng/0	involves: FVB/N	N	15657128
MGI:3831195	M	MP:0031365	prostate gland ventral lobe hyperplasia	Tg(Pbsn-Ar*E231G)7353Ng/0	involves: FVB/N	N	15657128
MGI:3831282	F	MP:0002169	no abnormal phenotype detected	Gt(ROSA)26Sor<tm1Sor>/Gt(ROSA)26Sor<+>,Hprt1<tm1(Pbsn*-cre/ERT2)Jir>/Hprt1<+>	involves: 129P2/OlaHsd * 129S4/SvJaeSor	N	18395839
MGI:3831293	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Hprt1<tm1(Pbsn*-cre/ERT2)Jir>/Y,Pten<tm2Mak>/Pten<tm2Mak>	involves: 129P2/OlaHsd * C57BL/6	N	19081794
MGI:3831293	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Hprt1<tm1(Pbsn*-cre/ERT2)Jir>/Y,Pten<tm2Mak>/Pten<tm2Mak>	involves: 129P2/OlaHsd * C57BL/6	N	19081794
MGI:3831295	F	MP:0001923	reduced female fertility	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * RBF/Dn	N	9070925
MGI:3831295	M	MP:0001925	male infertility	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * RBF/Dn	N	9070925
MGI:3831310	M	MP:0000858	abnormal metastatic potential	Tg(Pbsn-IGF1*)5305Ng/0,Tg(TRAMP)8247Ng/0	involves: C57BL/6 * FVB/N	N	18026134
MGI:3831310	M	MP:0002052	decreased tumor incidence	Tg(Pbsn-IGF1*)5305Ng/0,Tg(TRAMP)8247Ng/0	involves: C57BL/6 * FVB/N	N	18026134
MGI:3831310	M	MP:0010357	increased prostate gland tumor incidence	Tg(Pbsn-IGF1*)5305Ng/0,Tg(TRAMP)8247Ng/0	involves: C57BL/6 * FVB/N	N	18026134
MGI:3831312	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-IGF1*)5305Ng/0	involves: FVB/N	N	18026134
MGI:3831312	M	MP:0001168	abnormal prostate gland epithelium morphology	Tg(Pbsn-IGF1*)5305Ng/0	involves: FVB/N	N	18026134
MGI:3831312	M	MP:0001158	abnormal prostate gland morphology	Tg(Pbsn-IGF1*)5305Ng/0	involves: FVB/N	N	18026134
MGI:3831321	M	MP:0001925	male infertility	Tlr6<m4Btlr>/Tlr6<m4Btlr>	C57BL/6J-Tlr6<m4Btlr>	N	MGI:3830261
MGI:3831388	M	MP:0001147	small testis	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	N	9070925
MGI:3831388	M	MP:0001925	male infertility	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	N	9070925
MGI:3831388	M	MP:0001940	testis hypoplasia	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	N	10589692
MGI:3831388	F	MP:0001923	reduced female fertility	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	N	9070925
MGI:3831388	M	MP:0001156	abnormal spermatogenesis	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	N	10589692
MGI:3831435	F	MP:0001926	female infertility	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	N	9537225
MGI:3831435	M	MP:0001925	male infertility	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	N	9537225
MGI:3831658	M	MP:0005389	reproductive system phenotype	Ica1<tm1Mdos>/Ica1<tm1Mdos>	involves: 129S1/Sv * 129X1/SvJ	Y	26306493
MGI:3831882	M	MP:0002216	abnormal seminiferous tubule morphology	Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>	involves: 129S6/SvEvTac * C57BL/6	N	18936156
MGI:3831882	M	MP:0001156	abnormal spermatogenesis	Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>	involves: 129S6/SvEvTac * C57BL/6	N	18936156
MGI:3831882	M	MP:0014052	increased male germ cell apoptosis	Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>	involves: 129S6/SvEvTac * C57BL/6	N	18936156
MGI:3831882	M	MP:0001147	small testis	Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>	involves: 129S6/SvEvTac * C57BL/6	N	18936156
MGI:3831882	M	MP:0001922	reduced male fertility	Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>	involves: 129S6/SvEvTac * C57BL/6	N	18936156
MGI:3831883	M	MP:0001156	abnormal spermatogenesis	Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * SJL	N	18936156
MGI:3831883	M	MP:0004901	decreased male germ cell number	Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * SJL	N	18936156
MGI:3831884	M	MP:0001156	abnormal spermatogenesis	Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>,Terc<tm1Rdp>/Terc<+>	involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * SJL	N	18936156
MGI:3831884	M	MP:0001147	small testis	Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>,Terc<tm1Rdp>/Terc<+>	involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * SJL	N	18936156
MGI:3831884	M	MP:0004901	decreased male germ cell number	Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>,Terc<tm1Rdp>/Terc<+>	involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * SJL	N	18936156
MGI:3831885	M	MP:0001147	small testis	Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>	involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * SJL	N	18936156
MGI:3831885	M	MP:0004901	decreased male germ cell number	Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>	involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * SJL	N	18936156
MGI:3832352	F	MP:0001382	abnormal nursing	Tmie<sr>/Tmie<sr>	C57BL/How-Tmie<sr>	N	14027064
MGI:3832448	F	MP:0004259	small placenta	Amot<tm1Bhr>/Amot<tm1Bhr>	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832448	F	MP:0003229	abnormal vitelline vasculature morphology	Amot<tm1Bhr>/Amot<tm1Bhr>	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832448	F	MP:0003658	abnormal capillary morphology	Amot<tm1Bhr>/Amot<tm1Bhr>	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832448	F	MP:0004938	dilated vasculature	Amot<tm1Bhr>/Amot<tm1Bhr>	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832448	F	MP:0000260	abnormal angiogenesis	Amot<tm1Bhr>/Amot<tm1Bhr>	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832448	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Amot<tm1Bhr>/Amot<tm1Bhr>	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832448	F	MP:0001698	decreased embryo size	Amot<tm1Bhr>/Amot<tm1Bhr>	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832448	F	MP:0004950	abnormal brain vasculature morphology	Amot<tm1Bhr>/Amot<tm1Bhr>	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832462	M	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Amot<tm1Bhr>/Y	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832462	M	MP:0004950	abnormal brain vasculature morphology	Amot<tm1Bhr>/Y	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832462	M	MP:0000260	abnormal angiogenesis	Amot<tm1Bhr>/Y	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832462	M	MP:0004259	small placenta	Amot<tm1Bhr>/Y	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832462	M	MP:0003658	abnormal capillary morphology	Amot<tm1Bhr>/Y	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832462	M	MP:0001698	decreased embryo size	Amot<tm1Bhr>/Y	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832462	M	MP:0004938	dilated vasculature	Amot<tm1Bhr>/Y	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832462	M	MP:0003229	abnormal vitelline vasculature morphology	Amot<tm1Bhr>/Y	B6.129S7-Amot<tm1Bhr>	N	17699752
MGI:3832476	M	MP:0011092	embryonic lethality, complete penetrance	It/Y	Not Specified	N	MGI:61680
MGI:3832477	F	MP:0004790	absent upper incisors	It/It<+>	Not Specified	N	MGI:61680
MGI:3832477	F	MP:0001935	decreased litter size	It/It<+>	Not Specified	N	MGI:61680
MGI:3832477	F	MP:0030080	small lower incisors	It/It<+>	Not Specified	N	MGI:61680
MGI:3832477	F	MP:0005358	abnormal incisor morphology	It/It<+>	Not Specified	N	MGI:61680
MGI:3832477	F	MP:0000116	abnormal tooth development	It/It<+>	Not Specified	N	MGI:61680
MGI:3832477	F	MP:0004791	absent lower incisors	It/It<+>	Not Specified	N	MGI:61680
MGI:3832477	F	MP:0008770	decreased survivor rate	It/It<+>	Not Specified	N	MGI:61680
MGI:3832511	M	MP:0003136	yellow coat color	Crm<J>/Y	A/J-Crm<J>/J	N	MGI:78592
MGI:3832512	F	MP:0003136	yellow coat color	Crm<J>/Crm<+>	A/J-Crm<J>/J	N	MGI:78592
MGI:3832512	F	MP:0005366	variegated coat color	Crm<J>/Crm<+>	A/J-Crm<J>/J	N	MGI:78592
MGI:3832513	F	MP:0003136	yellow coat color	Crm<J>/Crm<J>	A/J-Crm<J>/J	N	MGI:78592
MGI:3832515	F	MP:0003136	yellow coat color	Crm<3J>/Crm<+>	FVB/NJ-Crm<3J>/J	N	MGI:3832510
MGI:3832515	F	MP:0005366	variegated coat color	Crm<3J>/Crm<+>	FVB/NJ-Crm<3J>/J	N	MGI:3832510
MGI:3832516	F	MP:0003136	yellow coat color	Crm<3J>/Crm<3J>	FVB/NJ-Crm<3J>/J	N	MGI:3832510
MGI:3832517	M	MP:0003136	yellow coat color	Crm<3J>/Y	FVB/NJ-Crm<3J>/J	N	MGI:3832510
MGI:3832595	F	MP:0008871	abnormal ovarian follicle number	Tg(Amhr2-Pik3ca*,-GFP)#Lzh/0	involves: C3H * C57BL/6	N	19172191
MGI:3832595	F	MP:0001126	abnormal ovary morphology	Tg(Amhr2-Pik3ca*,-GFP)#Lzh/0	involves: C3H * C57BL/6	N	19172191
MGI:3832595	F	MP:0001923	reduced female fertility	Tg(Amhr2-Pik3ca*,-GFP)#Lzh/0	involves: C3H * C57BL/6	N	19172191
MGI:3832664	M	MP:0005385	cardiovascular system phenotype	Fhl1<tm1Chen>/Y,Tg(Myh6-Gnaq)25Gwd/0	involves: 129S1/Sv * 129X1/SvJ * Black Swiss * FVB/N	Y	19033658
MGI:3832677	M	MP:0008469	abnormal protein level	Hprt1<tm1(AGT)Asku>/Y,Tg(REN)64071Sig/?	involves: 129P2/OlaHsd * C57BL/6	N	18945948
MGI:3832677	M	MP:0031232	increased circulating angiotensin II level	Hprt1<tm1(AGT)Asku>/Y,Tg(REN)64071Sig/?	involves: 129P2/OlaHsd * C57BL/6	N	18945948
MGI:3832677	M	MP:0006144	increased systemic arterial systolic blood pressure	Hprt1<tm1(AGT)Asku>/Y,Tg(REN)64071Sig/?	involves: 129P2/OlaHsd * C57BL/6	N	18945948
MGI:3832677	M	MP:0006373	abnormal circulating angiotensinogen level	Hprt1<tm1(AGT)Asku>/Y,Tg(REN)64071Sig/?	involves: 129P2/OlaHsd * C57BL/6	N	18945948
MGI:3832678	M	MP:0006373	abnormal circulating angiotensinogen level	Hprt1<tm2(AGT)Asku>/Y,Tg(REN)64071Sig/?	involves: 129P2/OlaHsd * C57BL/6	N	18945948
MGI:3832678	M	MP:0008469	abnormal protein level	Hprt1<tm2(AGT)Asku>/Y,Tg(REN)64071Sig/?	involves: 129P2/OlaHsd * C57BL/6	N	18945948
MGI:3832678	M	MP:0006144	increased systemic arterial systolic blood pressure	Hprt1<tm2(AGT)Asku>/Y,Tg(REN)64071Sig/?	involves: 129P2/OlaHsd * C57BL/6	N	18945948
MGI:3832678	M	MP:0031232	increased circulating angiotensin II level	Hprt1<tm2(AGT)Asku>/Y,Tg(REN)64071Sig/?	involves: 129P2/OlaHsd * C57BL/6	N	18945948
MGI:3832684	M	MP:0000745	tremors	Mecp2<tm2Bird>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	17289941
MGI:3832684	M	MP:0001513	limb grasping	Mecp2<tm2Bird>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	17289941
MGI:3832684	M	MP:0005386	behavior/neurological phenotype	Mecp2<tm2Bird>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	Y	17289941
MGI:3832684	M	MP:0001951	abnormal breathing pattern	Mecp2<tm2Bird>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	17289941
MGI:3832684	M	MP:0002083	premature death	Mecp2<tm2Bird>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	17289941
MGI:3832684	M	MP:0004924	abnormal behavior	Mecp2<tm2Bird>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	17289941
MGI:3832875	M	MP:0001156	abnormal spermatogenesis	bpck/bpck	B6C3Fe a/a-bpck/J	N	19211713
MGI:3832875	F	MP:0001127	small ovary	bpck/bpck	B6C3Fe a/a-bpck/J	N	19211713
MGI:3832875	M	MP:0001147	small testis	bpck/bpck	B6C3Fe a/a-bpck/J	N	19211713
MGI:3833237	F	MP:0001142	abnormal vagina orifice morphology	ipv/ipv	Not Specified	N	2614062
MGI:3833237	F	MP:0009085	abnormal uterine horn morphology	ipv/ipv	Not Specified	N	2614062
MGI:3833237	F	MP:0009087	dilated uterine horn	ipv/ipv	Not Specified	N	2614062
MGI:3833237	F	MP:0003540	imperforate hymen	ipv/ipv	Not Specified	N	2614062
MGI:3833426	M	MP:0001454	abnormal cued conditioning behavior	Gdi1<tm1Toni>/Y	either: B6.129S7-Gdi1<tm1Toni> or (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * DBA/2)	N	12354782
MGI:3833426	M	MP:0005394	taste/olfaction phenotype	Gdi1<tm1Toni>/Y	either: B6.129S7-Gdi1<tm1Toni> or (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * DBA/2)	Y	12354782
MGI:3833426	M	MP:0002761	abnormal hippocampal mossy fiber morphology	Gdi1<tm1Toni>/Y	either: B6.129S7-Gdi1<tm1Toni> or (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * DBA/2)	N	12354782
MGI:3833426	M	MP:0005376	homeostasis/metabolism phenotype	Gdi1<tm1Toni>/Y	either: B6.129S7-Gdi1<tm1Toni> or (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * DBA/2)	Y	12354782
MGI:3833426	M	MP:0008267	abnormal hippocampus CA3 region morphology	Gdi1<tm1Toni>/Y	either: B6.129S7-Gdi1<tm1Toni> or (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * DBA/2)	N	12354782
MGI:3833426	M	MP:0003863	decreased aggression towards mice	Gdi1<tm1Toni>/Y	either: B6.129S7-Gdi1<tm1Toni> or (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * DBA/2)	N	12354782
MGI:3833426	M	MP:0002912	abnormal excitatory postsynaptic potential	Gdi1<tm1Toni>/Y	either: B6.129S7-Gdi1<tm1Toni> or (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * DBA/2)	N	12354782
MGI:3833426	M	MP:0008428	abnormal spatial working memory	Gdi1<tm1Toni>/Y	either: B6.129S7-Gdi1<tm1Toni> or (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * DBA/2)	N	12354782
MGI:3833428	M	MP:0004494	abnormal synaptic glutamate release	Gdi1<tm1Toni>/Y	B6N.129S7-Gdi1<tm1Toni>	N	18829665
MGI:3833428	M	MP:0002912	abnormal excitatory postsynaptic potential	Gdi1<tm1Toni>/Y	B6N.129S7-Gdi1<tm1Toni>	N	18829665
MGI:3833428	M	MP:0001454	abnormal cued conditioning behavior	Gdi1<tm1Toni>/Y	B6N.129S7-Gdi1<tm1Toni>	N	18829665
MGI:3833428	M	MP:0002919	enhanced paired-pulse facilitation	Gdi1<tm1Toni>/Y	B6N.129S7-Gdi1<tm1Toni>	N	18829665
MGI:3833428	M	MP:0004495	decreased synaptic glutamate release	Gdi1<tm1Toni>/Y	B6N.129S7-Gdi1<tm1Toni>	N	18829665
MGI:3833428	M	MP:0004792	abnormal synaptic vesicle number	Gdi1<tm1Toni>/Y	B6N.129S7-Gdi1<tm1Toni>	N	18829665
MGI:3833428	M	MP:0008428	abnormal spatial working memory	Gdi1<tm1Toni>/Y	B6N.129S7-Gdi1<tm1Toni>	N	18829665
MGI:3833431	F	MP:0008779	abnormal maternal behavior	hubb/hubb	involves: ICR	N	4086788
MGI:3833431	M	MP:0001925	male infertility	hubb/hubb	involves: ICR	N	4086788
MGI:3833431	F	MP:0001385	pup cannibalization	hubb/hubb	involves: ICR	N	10627055
MGI:3833431	M	MP:0001156	abnormal spermatogenesis	hubb/hubb	involves: ICR	N	4086788
MGI:3833431	M	MP:0001147	small testis	hubb/hubb	involves: ICR	N	4086788
MGI:3833431	F	MP:0009327	abnormal maternal grooming	hubb/hubb	involves: ICR	N	10627055
MGI:3833431	F	MP:0008779	abnormal maternal behavior	hubb/hubb	involves: ICR	N	10627055
MGI:3833431	F	MP:0001386	abnormal maternal nurturing	hubb/hubb	involves: ICR	N	10627055
MGI:3833431	M	MP:0005159	azoospermia	hubb/hubb	involves: ICR	N	4086788
MGI:3833431	F	MP:0001386	abnormal maternal nurturing	hubb/hubb	involves: ICR	N	4086788
MGI:3833431	M	MP:0001150	enlarged scrotum	hubb/hubb	involves: ICR	N	4086788
MGI:3833560	F	MP:0001923	reduced female fertility	Nrarp<tm1Vlcg>/Nrarp<tm1Vlcg>	involves: C57BL/6J	N	19154719
MGI:3833574	F	MP:0002777	absent ovarian follicles	Kitl<Sl-J>/Kitl<Sl-J>	C3HeB/FeHu-Kitl<Sl-J>	N	MGI:3833567
MGI:3833574	M	MP:0002216	abnormal seminiferous tubule morphology	Kitl<Sl-J>/Kitl<Sl-J>	C3HeB/FeHu-Kitl<Sl-J>	N	MGI:3833567
MGI:3833649	M	MP:0004478	increased testicular teratoma incidence	Kitl<Sl-J>/Kitl<+>	involves: 129	N	MGI:1306770
MGI:3834157	M	MP:0008327	abnormal corticotroph morphology	Sytl4<tm1Tiz>/Y	involves: 129P2/OlaHsd	N	17761531
MGI:3834157	M	MP:0001747	hypersecretion of adrenocorticotropin	Sytl4<tm1Tiz>/Y	involves: 129P2/OlaHsd	N	17761531
MGI:3834182	M	MP:0001158	abnormal prostate gland morphology	Eaf2<tm1Zhow>/Eaf2<tm1Zhow>	involves: 129P2/OlaHsd * C57BL/6J	N	17873910
MGI:3834182	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Eaf2<tm1Zhow>/Eaf2<tm1Zhow>	involves: 129P2/OlaHsd * C57BL/6J	N	17873910
MGI:3834182	M	MP:0001168	abnormal prostate gland epithelium morphology	Eaf2<tm1Zhow>/Eaf2<tm1Zhow>	involves: 129P2/OlaHsd * C57BL/6J	N	17873910
MGI:3834182	M	MP:0004961	increased prostate gland weight	Eaf2<tm1Zhow>/Eaf2<tm1Zhow>	involves: 129P2/OlaHsd * C57BL/6J	N	17873910
MGI:3834197	F	MP:0001923	reduced female fertility	Asph<tm1Jed>/Asph<tm1Jed>	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	11773073
MGI:3834458	M	MP:0002216	abnormal seminiferous tubule morphology	Apex1<tm1Djc>/Apex1<+>	involves: 129X1/SvJ * NTac:NIHS	N	15340075
MGI:3834481	M	MP:0006262	increased testis tumor incidence	Tg(Ly6a-BCR/ABL1)IS1AIsg/0	involves: C57BL/6J * CBA	N	19037256
MGI:3834482	M	MP:0006262	increased testis tumor incidence	Tg(Ly6a-BCR/ABL1)IS1BIsg/0	involves: C57BL/6J * CBA	N	19037256
MGI:3834597	M	MP:0001360	abnormal social investigation	Gria1<tm1Erk>/Gria1<tm1Erk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15344919
MGI:3834597	M	MP:0002566	abnormal sexual interaction	Gria1<tm1Erk>/Gria1<tm1Erk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	15344919
MGI:3834600	F	MP:0001923	reduced female fertility	Lpp<tm1Wjmv>/Lpp<tm1Wjmv>	B6.129P2-Lpp<tm1Wjmv>	N	19111675
MGI:3834745	M	MP:0003607	abnormal prostate gland physiology	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(tetO-BRAF*V600E)29Lc/0,Tg(Tyr-rtTA)37Lc/0	involves: 129/Sv * C57BL/6J * SJL	N	19079609
MGI:3834745	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(tetO-BRAF*V600E)29Lc/0,Tg(Tyr-rtTA)37Lc/0	involves: 129/Sv * C57BL/6J * SJL	N	19079609
MGI:3834745	M	MP:0000659	prostate gland hyperplasia	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(tetO-BRAF*V600E)29Lc/0,Tg(Tyr-rtTA)37Lc/0	involves: 129/Sv * C57BL/6J * SJL	N	19079609
MGI:3834842	F	MP:0009013	abnormal proestrus	Magel2<tm1Stw>/Magel2<+>	C57BL/6-Magel2<tm1Stw>	N	19172181
MGI:3834842	F	MP:0002679	abnormal corpus luteum morphology	Magel2<tm1Stw>/Magel2<+>	C57BL/6-Magel2<tm1Stw>	N	19172181
MGI:3834842	F	MP:0009006	prolonged estrous cycle	Magel2<tm1Stw>/Magel2<+>	C57BL/6-Magel2<tm1Stw>	N	19172181
MGI:3834842	F	MP:0001385	pup cannibalization	Magel2<tm1Stw>/Magel2<+>	C57BL/6-Magel2<tm1Stw>	N	19172181
MGI:3834848	M	MP:0005241	abnormal retina ganglion layer morphology	Atrx<tm1Rjg>/Y,Tg(Pax6-cre,GFP)2Pgr/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	19088125
MGI:3834848	M	MP:0005551	abnormal eye electrophysiology	Atrx<tm1Rjg>/Y,Tg(Pax6-cre,GFP)2Pgr/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	19088125
MGI:3834848	M	MP:0003733	abnormal retina inner nuclear layer morphology	Atrx<tm1Rjg>/Y,Tg(Pax6-cre,GFP)2Pgr/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	19088125
MGI:3834848	M	MP:0006068	abnormal retina horizontal cell morphology	Atrx<tm1Rjg>/Y,Tg(Pax6-cre,GFP)2Pgr/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	19088125
MGI:3834848	M	MP:0001325	abnormal retina morphology	Atrx<tm1Rjg>/Y,Tg(Pax6-cre,GFP)2Pgr/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	19088125
MGI:3834848	M	MP:0008106	decreased amacrine cell number	Atrx<tm1Rjg>/Y,Tg(Pax6-cre,GFP)2Pgr/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	19088125
MGI:3834940	M	MP:0001147	small testis	Hmga2<pg-Tg40ACha>/Hmga2<pg-Tg40ACha>	involves: C57BL/6J * CBA/J	N	7958830
MGI:3834943	M	MP:0001147	small testis	Hmga2<pg-Tg40ACha>/Hmga2<+>	involves: C57BL/6J * CBA/J	N	7958830
MGI:3835031	M	MP:0001156	abnormal spermatogenesis	Tg(BCL2OVARY)1Ah/0	involves: FVB	N	11700863
MGI:3835031	M	MP:0002784	abnormal Sertoli cell morphology	Tg(BCL2OVARY)1Ah/0	involves: FVB	N	11700863
MGI:3835031	M	MP:0002216	abnormal seminiferous tubule morphology	Tg(BCL2OVARY)1Ah/0	involves: FVB	N	11700863
MGI:3835031	M	MP:0004852	decreased testis weight	Tg(BCL2OVARY)1Ah/0	involves: FVB	N	11700863
MGI:3835031	F	MP:0031421	increased superovulation rate	Tg(BCL2OVARY)1Ah/0	involves: FVB	N	8895354
MGI:3835031	F	MP:0031016	decreased granulosa cell apoptosis	Tg(BCL2OVARY)1Ah/0	involves: FVB	N	8895354
MGI:3835031	M	MP:0014052	increased male germ cell apoptosis	Tg(BCL2OVARY)1Ah/0	involves: FVB	N	11700863
MGI:3835031	M	MP:0006380	abnormal spermatid morphology	Tg(BCL2OVARY)1Ah/0	involves: FVB	N	11700863
MGI:3835031	M	MP:0004901	decreased male germ cell number	Tg(BCL2OVARY)1Ah/0	involves: FVB	N	11700863
MGI:3835031	F	MP:0009442	increased ovarian teratoma incidence	Tg(BCL2OVARY)1Ah/0	involves: FVB	N	8895354
MGI:3835048	M	MP:0001922	reduced male fertility	Gabrg2<tm1Geh>/Gabrg2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	10218866
MGI:3835107	F	MP:0001382	abnormal nursing	eob/eob	involves: NC	N	1460847
MGI:3835107	F	MP:0001386	abnormal maternal nurturing	eob/eob	involves: NC	N	1460847
MGI:3835117	F	MP:0000630	mammary gland hyperplasia	Tg(WapTAg)3Knw/0	C57BL/6J-Tg(WapTAg)3Knw	N	9859214
MGI:3835117	F	MP:0001382	abnormal nursing	Tg(WapTAg)3Knw/0	C57BL/6J-Tg(WapTAg)3Knw	N	9859214
MGI:3835320	F	MP:0008779	abnormal maternal behavior	Cux1<tm1Ejn>/Cux1<tm1Ejn>	involves: 129S4/SvJae * C57BL	N	9698457
MGI:3835333	F	MP:0001923	reduced female fertility	Tg(TTR-p19Cdkn2a)2Tvd/0	involves: C57BL/6J * DBA/2J	N	MGI:3510987
MGI:3835423	F	MP:0000630	mammary gland hyperplasia	Tg(C3-1-TAg)cJeg/0	involves: FVB/N	N	9502400
MGI:3835423	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(C3-1-TAg)cJeg/0	involves: FVB/N	N	7972041
MGI:3835423	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(C3-1-TAg)cJeg/0	involves: FVB/N	N	9502400
MGI:3835423	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(C3-1-TAg)cJeg/0	involves: FVB/N	N	8895741
MGI:3835423	M	MP:0001167	prostate gland epithelial hyperplasia	Tg(C3-1-TAg)cJeg/0	involves: FVB/N	N	7972041
MGI:3835423	M	MP:0003607	abnormal prostate gland physiology	Tg(C3-1-TAg)cJeg/0	involves: FVB/N	N	9502400
MGI:3835423	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(C3-1-TAg)cJeg/0	involves: FVB/N	N	9502400
MGI:3835423	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(C3-1-TAg)cJeg/0	involves: FVB/N	N	7972041
MGI:3835423	F	MP:0001885	mammary gland duct hyperplasia	Tg(C3-1-TAg)cJeg/0	involves: FVB/N	N	7972041
MGI:3835423	M	MP:0011791	increased bulbourethral gland adenocarcinoma incidence	Tg(C3-1-TAg)cJeg/0	involves: FVB/N	N	9502400
MGI:3835423	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(C3-1-TAg)cJeg/0	involves: FVB/N	N	7972041
MGI:3835423	M	MP:0011790	increased urethral gland adenocarcinoma incidence	Tg(C3-1-TAg)cJeg/0	involves: FVB/N	N	9502400
MGI:3835423	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(C3-1-TAg)cJeg/0	involves: FVB/N	N	8895741
MGI:3835424	F	MP:0001923	reduced female fertility	Tg(Zp3-cre)3Mrt/Tg(Zp3-cre)3Mrt	FVB/N-Tg(Zp3-cre)3Mrt/J	N	10686600
MGI:3835441	F	MP:0001923	reduced female fertility	Tg(Zp3-cre)3Mrt/0	B6.FVB-Tg(Zp3-cre)3Mrt	N	10686600
MGI:3835482	F	MP:0000629	absent mammary gland	Hr<ba>/Hr<ba>	Not Specified	N	MGI:61276
MGI:3835482	F	MP:0013529	decreased nipple number	Hr<ba>/Hr<ba>	Not Specified	N	MGI:61276
MGI:3835482	F	MP:0009722	abnormal nipple development	Hr<ba>/Hr<ba>	Not Specified	N	MGI:61276
MGI:3835576	M	MP:0001925	male infertility	Kmt2e<tm1.1Hjf>/Kmt2e<tm1.1Hjf>	B6.129P2-Kmte<tm1.1Hjf>	N	18952892
MGI:3835576	F	MP:0001923	reduced female fertility	Kmt2e<tm1.1Hjf>/Kmt2e<tm1.1Hjf>	B6.129P2-Kmte<tm1.1Hjf>	N	18952892
MGI:3835576	M	MP:0002686	globozoospermia	Kmt2e<tm1.1Hjf>/Kmt2e<tm1.1Hjf>	B6.129P2-Kmte<tm1.1Hjf>	N	18952892
MGI:3835753	M	MP:0001925	male infertility	Rorb<m1Btlr>/Rorb<m1Btlr>	C57BL/6J-Rorb<m1Btlr>	N	MGI:3835555
MGI:3835787	M	MP:0002662	abnormal cauda epididymis morphology	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	22069496
MGI:3835787	M	MP:0009232	abnormal sperm nucleus morphology	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	22069496
MGI:3835787	M	MP:0001925	male infertility	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	18854576
MGI:3835787	M	MP:0013320	dilated seminal vesicle	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	18854576
MGI:3835787	M	MP:0005376	homeostasis/metabolism phenotype	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	Y	22069496
MGI:3835787	M	MP:0001932	abnormal spermiogenesis	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	22069496
MGI:3835787	M	MP:0002675	asthenozoospermia	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	22069496
MGI:3835787	M	MP:0030976	impaired sperm penetration of zona pellucida	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	22069496
MGI:3835787	F	MP:0005389	reproductive system phenotype	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	Y	22069496
MGI:3835787	M	MP:0009230	abnormal sperm head morphology	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	22069496
MGI:3835787	M	MP:0009231	detached acrosome	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	22069496
MGI:3835787	M	MP:0001156	abnormal spermatogenesis	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	22069496
MGI:3835787	M	MP:0000242	impaired fertilization	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	22069496
MGI:3835787	M	MP:0008898	abnormal acrosome morphology	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	22069496
MGI:3835787	M	MP:0020451	decreased sperm progressive motility	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	22069496
MGI:3835787	M	MP:0001925	male infertility	Kmt2e<tm1Apa>/Kmt2e<tm1Apa>	129S6/SvEvTac-Kmt2e<tm1Apa>	N	22069496
MGI:3835820	M	MP:0004852	decreased testis weight	Rad18<tm1Stat>/Rad18<tm1Stat>	B6.Cg-Rad18<tm1Stat>	N	19068231
MGI:3835820	M	MP:0004901	decreased male germ cell number	Rad18<tm1Stat>/Rad18<tm1Stat>	B6.Cg-Rad18<tm1Stat>	N	19068231
MGI:3835820	M	MP:0006378	abnormal spermatogonia morphology	Rad18<tm1Stat>/Rad18<tm1Stat>	B6.Cg-Rad18<tm1Stat>	N	19068231
MGI:3835820	M	MP:0001922	reduced male fertility	Rad18<tm1Stat>/Rad18<tm1Stat>	B6.Cg-Rad18<tm1Stat>	N	19068231
MGI:3835820	M	MP:0001154	seminiferous tubule degeneration	Rad18<tm1Stat>/Rad18<tm1Stat>	B6.Cg-Rad18<tm1Stat>	N	19068231
MGI:3835838	M	MP:0004802	decreased susceptibility to systemic lupus erythematosus	Il21r<tm1Wjl>/Il21r<tm1Wjl>,X/Yaa	BXSB.129(Cg)-Il21r<tm1Wjl>/Dcr	N	19164519
MGI:3835838	M	MP:0010768	mortality/aging	Il21r<tm1Wjl>/Il21r<tm1Wjl>,X/Yaa	BXSB.129(Cg)-Il21r<tm1Wjl>/Dcr	Y	19164519
MGI:3835838	M	MP:0010768	mortality/aging	Il21r<tm1Wjl>/Il21r<tm1Wjl>,X/Yaa	BXSB.129(Cg)-Il21r<tm1Wjl>/Dcr	Y	21964024
MGI:3836157	F	MP:0001885	mammary gland duct hyperplasia	Tg(MMTV-AURKA)#Cxd/?	involves: FVB/N	N	16715125
MGI:3836157	F	MP:0008000	increased ovary tumor incidence	Tg(MMTV-AURKA)#Cxd/?	involves: FVB/N	N	16715125
MGI:3836157	F	MP:0009504	abnormal mammary gland epithelium morphology	Tg(MMTV-AURKA)#Cxd/?	involves: FVB/N	N	16715125
MGI:3836157	F	MP:0002676	uterus hyperplasia	Tg(MMTV-AURKA)#Cxd/?	involves: FVB/N	N	16715125
MGI:3836157	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(MMTV-AURKA)#Cxd/?	involves: FVB/N	N	16715125
MGI:3836157	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(MMTV-AURKA)#Cxd/?	involves: FVB/N	N	16715125
MGI:3836157	F	MP:0000630	mammary gland hyperplasia	Tg(MMTV-AURKA)#Cxd/?	involves: FVB/N	N	16715125
MGI:3836158	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(MMTV-AURKA)#Cxd/?,Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas * FVB/N	N	16715125
MGI:3836158	F	MP:0001885	mammary gland duct hyperplasia	Tg(MMTV-AURKA)#Cxd/?,Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas * FVB/N	N	16715125
MGI:3836158	F	MP:0009504	abnormal mammary gland epithelium morphology	Tg(MMTV-AURKA)#Cxd/?,Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas * FVB/N	N	16715125
MGI:3836474	M	MP:0003205	testicular atrophy	Ercc3<tm2Jhjh>/Ercc3<tm2Jhjh>,Xpa<tm1Hvs>/Xpa<tm1Hvs>	involves: 129P2/OlaHsd * C57BL/6	N	19114557
MGI:3836561	F	MP:0002459	abnormal B cell physiology	Blnk<tm1Achn>/Blnk<+>,Btk<tm1Wk>/Btk<tm1Wk>,Tg(IGH-Btk)1Witt/0	involves: 129S4/SvJae * 129X1/SvJ * BALB/c * C3H * C57BL/6	N	12618482
MGI:3836561	F	MP:0005093	decreased B cell proliferation	Blnk<tm1Achn>/Blnk<+>,Btk<tm1Wk>/Btk<tm1Wk>,Tg(IGH-Btk)1Witt/0	involves: 129S4/SvJae * 129X1/SvJ * BALB/c * C3H * C57BL/6	N	12618482
MGI:3836562	F	MP:0005093	decreased B cell proliferation	Btk<tm1Wk>/Btk<tm1Wk>,Tg(IGH-Btk)1Witt/0	involves: 129S4/SvJae * 129X1/SvJ * BALB/c * C3H * C57BL/6	N	12618482
MGI:3836577	M	MP:0000659	prostate gland hyperplasia	Kras<tm1Bbd>/Kras<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	19117991
MGI:3836577	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Kras<tm1Bbd>/Kras<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	19117991
MGI:3836577	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Kras<tm1Bbd>/Kras<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	19117991
MGI:3836578	M	MP:0013733	squamous metaplasia of bulbourethral gland	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Kras<tm1Bbd>/Kras<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	19117991
MGI:3836578	M	MP:0010357	increased prostate gland tumor incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Kras<tm1Bbd>/Kras<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	19117991
MGI:3836579	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Tg(Pbsn-cre)4Prb/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	19117991
MGI:3836579	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Tg(Pbsn-cre)4Prb/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	19117991
MGI:3836579	M	MP:0013733	squamous metaplasia of bulbourethral gland	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Tg(Pbsn-cre)4Prb/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	19117991
MGI:3836579	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Tg(Pbsn-cre)4Prb/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	31819003
MGI:3836579	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Tg(Pbsn-cre)4Prb/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	31819003
MGI:3836627	M	MP:0001922	reduced male fertility	Aire<tm1Ptsn>/Aire<tm1Ptsn>	C57BL/6-Aire<tm1Ptsn>	N	19265170
MGI:3836730	M	MP:0001844	autoimmune response	Bxs6<BXSB/MpJ>/Bxs6<BXSB/MpJ>,X/Yaa	B10.BXSB-(D13Mit3-D13Mit78) Yaa	N	17371996
MGI:3836730	M	MP:0004762	increased anti-double stranded DNA antibody level	Bxs6<BXSB/MpJ>/Bxs6<BXSB/MpJ>,X/Yaa	B10.BXSB-(D13Mit3-D13Mit78) Yaa	N	17371996
MGI:3836730	M	MP:0002743	glomerulonephritis	Bxs6<BXSB/MpJ>/Bxs6<BXSB/MpJ>,X/Yaa	B10.BXSB-(D13Mit3-D13Mit78) Yaa	N	17371996
MGI:3836730	M	MP:0004771	increased anti-single stranded DNA antibody level	Bxs6<BXSB/MpJ>/Bxs6<BXSB/MpJ>,X/Yaa	B10.BXSB-(D13Mit3-D13Mit78) Yaa	N	17371996
MGI:3836730	M	MP:0003725	increased autoantibody level	Bxs6<BXSB/MpJ>/Bxs6<BXSB/MpJ>,X/Yaa	B10.BXSB-(D13Mit3-D13Mit78) Yaa	N	17371996
MGI:3836730	M	MP:0000691	enlarged spleen	Bxs6<BXSB/MpJ>/Bxs6<BXSB/MpJ>,X/Yaa	B10.BXSB-(D13Mit3-D13Mit78) Yaa	N	17371996
MGI:3836755	F	MP:0003915	increased heart left ventricle weight	Cyp2j5<tm1Dcz>/Cyp2j5<tm1Dcz>	129S/SvEv-Cyp2j5<tm1Dcz>	N	18716027
MGI:3836755	F	MP:0011417	abnormal renal transport	Cyp2j5<tm1Dcz>/Cyp2j5<tm1Dcz>	129S/SvEv-Cyp2j5<tm1Dcz>	N	18716027
MGI:3836755	F	MP:0003025	increased vasoconstriction	Cyp2j5<tm1Dcz>/Cyp2j5<tm1Dcz>	129S/SvEv-Cyp2j5<tm1Dcz>	N	18716027
MGI:3836755	F	MP:0003371	decreased circulating estrogen level	Cyp2j5<tm1Dcz>/Cyp2j5<tm1Dcz>	129S/SvEv-Cyp2j5<tm1Dcz>	N	18716027
MGI:3836755	F	MP:0001935	decreased litter size	Cyp2j5<tm1Dcz>/Cyp2j5<tm1Dcz>	129S/SvEv-Cyp2j5<tm1Dcz>	N	18716027
MGI:3836755	F	MP:0006144	increased systemic arterial systolic blood pressure	Cyp2j5<tm1Dcz>/Cyp2j5<tm1Dcz>	129S/SvEv-Cyp2j5<tm1Dcz>	N	18716027
MGI:3836899	F	MP:0008190	decreased transitional stage B cell number	Btk<xid>/Btk<xid>	B6.CBA-Btk<xid>	N	17105816
MGI:3836904	F	MP:0001926	female infertility	Ppp1r13l<wa3-J>/Ppp1r13l<wa3-J>	BALB/cJ-Ppp1r13l<wa3-J>/J	N	MGI:3836902
MGI:3836904	M	MP:0001922	reduced male fertility	Ppp1r13l<wa3-J>/Ppp1r13l<wa3-J>	BALB/cJ-Ppp1r13l<wa3-J>/J	N	MGI:3836902
MGI:3837031	F	MP:0006271	abnormal involution of the mammary gland	Il6st<tm1Ard>/Il6st<tm1Ard>	involves: 129S1/Sv * C57BL/6	N	15292206
MGI:3837031	F	MP:0001728	failure of embryo implantation	Il6st<tm1Ard>/Il6st<tm1Ard>	involves: 129S1/Sv * C57BL/6	N	11457894
MGI:3837031	F	MP:0001926	female infertility	Il6st<tm1Ard>/Il6st<tm1Ard>	involves: 129S1/Sv * C57BL/6	N	11457894
MGI:3837431	M	MP:0002687	oligozoospermia	Tbpl1<tm1Saco>/Tbpl1<+>	involves: 129S2/SvPas * C57BL/6	N	11463376
MGI:3837853	F	MP:0001144	vagina atresia	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>	involves: C57BL/6J	N	18393392
MGI:3837853	M	MP:0009853	decreased Sertoli cell phagocytosis	Axl<tm1Grl>/Axl<tm1Grl>,Mertk<tm1Grl>/Mertk<tm1Grl>	involves: C57BL/6J	N	18159085
MGI:3838013	F	MP:0001923	reduced female fertility	Clic4<tm1Jce>/Clic4<tm1Jce>	involves: 129S1/Sv * CD-1	N	19197003
MGI:3838153	M	MP:0001922	reduced male fertility	Tg(Myh7-RARA/lacZ)30Mcco/0	Not Specified	N	9329959
MGI:3838226	F	MP:0005016	decreased lymphocyte cell number	Cr1l<tm1.1Song>/Cr1l<tm1.1Song>,Vsig4<tm1Gne>/Vsig4<tm1Gne>,Tg(Cd4-cre)1Cwi/0	involves: 129S6/SvEvTac * C57BL/6N * DBA/2 * SJL	N	19136662
MGI:3838352	F	MP:0011939	increased food intake	Agpat2<tm1Garg>/Agpat2<tm1Garg>	involves: 129S6/SvEvTac	N	26880786
MGI:3838352	F	MP:0005178	increased circulating cholesterol level	Agpat2<tm1Garg>/Agpat2<tm1Garg>	involves: 129S6/SvEvTac	N	26880786
MGI:3838352	M	MP:0005292	improved glucose tolerance	Agpat2<tm1Garg>/Agpat2<tm1Garg>	involves: 129S6/SvEvTac	N	26880786
MGI:3838352	F	MP:0005559	increased circulating glucose level	Agpat2<tm1Garg>/Agpat2<tm1Garg>	involves: 129S6/SvEvTac	N	26880786
MGI:3838362	F	MP:0001882	abnormal lactation	Id2<tm1Mais>/Id2<tm1Mais>	involves: 129X1/SvJ * C57BL/6	N	19217292
MGI:3838371	M	MP:0004852	decreased testis weight	Sun1<tm1.1Ktj>/Sun1<tm1.1Ktj>	involves: C57BL/6J * FVB/N	N	19211677
MGI:3838371	M	MP:0001147	small testis	Sun1<tm1.1Ktj>/Sun1<tm1.1Ktj>	involves: C57BL/6J * FVB/N	N	19211677
MGI:3838371	F	MP:0004805	absent oocytes	Sun1<tm1.1Ktj>/Sun1<tm1.1Ktj>	involves: C57BL/6J * FVB/N	N	19211677
MGI:3838371	F	MP:0001926	female infertility	Sun1<tm1.1Ktj>/Sun1<tm1.1Ktj>	involves: C57BL/6J * FVB/N	N	19211677
MGI:3838371	M	MP:0005159	azoospermia	Sun1<tm1.1Ktj>/Sun1<tm1.1Ktj>	involves: C57BL/6J * FVB/N	N	19211677
MGI:3838371	M	MP:0008261	arrest of male meiosis	Sun1<tm1.1Ktj>/Sun1<tm1.1Ktj>	involves: C57BL/6J * FVB/N	N	19211677
MGI:3838371	F	MP:0002777	absent ovarian follicles	Sun1<tm1.1Ktj>/Sun1<tm1.1Ktj>	involves: C57BL/6J * FVB/N	N	19211677
MGI:3838371	M	MP:0005169	abnormal male meiosis	Sun1<tm1.1Ktj>/Sun1<tm1.1Ktj>	involves: C57BL/6J * FVB/N	N	19211677
MGI:3838371	M	MP:0001925	male infertility	Sun1<tm1.1Ktj>/Sun1<tm1.1Ktj>	involves: C57BL/6J * FVB/N	N	19211677
MGI:3838389	M	MP:0006380	abnormal spermatid morphology	Usp1<tm1.1Ada>/Usp1<tm1.1Ada>	C57BL/6-Usp1<tm1.1Ada>	N	19217432
MGI:3838389	M	MP:0002687	oligozoospermia	Usp1<tm1.1Ada>/Usp1<tm1.1Ada>	C57BL/6-Usp1<tm1.1Ada>	N	19217432
MGI:3838389	F	MP:0001923	reduced female fertility	Usp1<tm1.1Ada>/Usp1<tm1.1Ada>	C57BL/6-Usp1<tm1.1Ada>	N	19217432
MGI:3838389	M	MP:0001147	small testis	Usp1<tm1.1Ada>/Usp1<tm1.1Ada>	C57BL/6-Usp1<tm1.1Ada>	N	19217432
MGI:3838389	F	MP:0005431	decreased oocyte number	Usp1<tm1.1Ada>/Usp1<tm1.1Ada>	C57BL/6-Usp1<tm1.1Ada>	N	19217432
MGI:3838389	M	MP:0001925	male infertility	Usp1<tm1.1Ada>/Usp1<tm1.1Ada>	C57BL/6-Usp1<tm1.1Ada>	N	19217432
MGI:3838389	M	MP:0006362	abnormal male germ cell morphology	Usp1<tm1.1Ada>/Usp1<tm1.1Ada>	C57BL/6-Usp1<tm1.1Ada>	N	19217432
MGI:3838389	M	MP:0006379	abnormal spermatocyte morphology	Usp1<tm1.1Ada>/Usp1<tm1.1Ada>	C57BL/6-Usp1<tm1.1Ada>	N	19217432
MGI:3838389	M	MP:0001154	seminiferous tubule degeneration	Usp1<tm1.1Ada>/Usp1<tm1.1Ada>	C57BL/6-Usp1<tm1.1Ada>	N	19217432
MGI:3838389	M	MP:0006378	abnormal spermatogonia morphology	Usp1<tm1.1Ada>/Usp1<tm1.1Ada>	C57BL/6-Usp1<tm1.1Ada>	N	19217432
MGI:3838390	M	MP:0001147	small testis	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	19217432
MGI:3838390	M	MP:0002216	abnormal seminiferous tubule morphology	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	19217432
MGI:3838390	F	MP:0002682	decreased mature ovarian follicle number	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	19217432
MGI:3838390	M	MP:0002687	oligozoospermia	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	19217432
MGI:3838390	M	MP:0005169	abnormal male meiosis	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	19217432
MGI:3838390	M	MP:0006379	abnormal spermatocyte morphology	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	19217432
MGI:3838391	F	MP:0004833	ovary atrophy	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>,Usp1<tm1.1Ada>/Usp1<tm1.1Ada>	involves: 129S5/SvEvBrd * C57BL/6	N	19217432
MGI:3838613	F	MP:0001926	female infertility	Ptx3<tm1Zuk>/Ptx3<tm1Zuk>	involves: 129S7/SvEvBrd	N	12040004
MGI:3838721	F	MP:0012035	abnormal b-wave shape	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	involves: C57BL/6	N	24163243
MGI:3838721	F	MP:0002090	abnormal vision	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	involves: C57BL/6	N	24163243
MGI:3838721	F	MP:0001006	abnormal retina cone cell morphology	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	involves: C57BL/6	N	24163243
MGI:3838721	F	MP:0006073	abnormal retina bipolar cell morphology	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	involves: C57BL/6	N	24163243
MGI:3838721	F	MP:0009392	retina gliosis	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	involves: C57BL/6	N	24163243
MGI:3838721	F	MP:0006068	abnormal retina horizontal cell morphology	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	involves: C57BL/6	N	24163243
MGI:3838721	F	MP:0003732	abnormal retina outer plexiform layer morphology	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	involves: C57BL/6	N	24163243
MGI:3838721	F	MP:0009538	abnormal synapse morphology	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	involves: C57BL/6	N	24163243
MGI:3838721	F	MP:0002001	blindness	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	involves: C57BL/6	N	24163243
MGI:3838721	F	MP:0008444	retina cone cell degeneration	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	involves: C57BL/6	N	24163243
MGI:3838721	F	MP:0003731	abnormal retina outer nuclear layer morphology	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	involves: C57BL/6	N	24163243
MGI:3838721	F	MP:0008519	thin retina outer plexiform layer	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	involves: C57BL/6	N	24163243
MGI:3838721	F	MP:0003734	abnormal retina inner plexiform layer morphology	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	involves: C57BL/6	N	24163243
MGI:3838857	F	MP:0005389	reproductive system phenotype	Ptx3<tm1Mant>/Ptx3<tm1Mant>	involves: 129S1/Sv * 129X1/SvJ	Y	14998931
MGI:3838857	F	MP:0001926	female infertility	Ptx3<tm1Mant>/Ptx3<tm1Mant>	involves: 129S1/Sv * 129X1/SvJ	N	14998931
MGI:3838857	F	MP:0000242	impaired fertilization	Ptx3<tm1Mant>/Ptx3<tm1Mant>	involves: 129S1/Sv * 129X1/SvJ	N	14998931
MGI:3838857	F	MP:0009374	absent cumulus expansion	Ptx3<tm1Mant>/Ptx3<tm1Mant>	involves: 129S1/Sv * 129X1/SvJ	N	17675295
MGI:3838857	F	MP:0009374	absent cumulus expansion	Ptx3<tm1Mant>/Ptx3<tm1Mant>	involves: 129S1/Sv * 129X1/SvJ	N	14998931
MGI:3838857	F	MP:0009372	abnormal cumulus oophorus morphology	Ptx3<tm1Mant>/Ptx3<tm1Mant>	involves: 129S1/Sv * 129X1/SvJ	N	14998931
MGI:3838858	F	MP:0001923	reduced female fertility	Ptx3<tm1Mant>/Ptx3<tm1Mant>	involves: 129 * C57BL/6J	N	14998931
MGI:3838963	M	MP:0001353	increased aggression towards mice	Tg(Camk2a-tTA)1Mmay/0,Tg(tetO-DISC1*)1001Plet/0	involves: C57BL/6 * CBA * SJL	N	17848917
MGI:3838963	F	MP:0008414	abnormal spatial reference memory	Tg(Camk2a-tTA)1Mmay/0,Tg(tetO-DISC1*)1001Plet/0	involves: C57BL/6 * CBA * SJL	N	17848917
MGI:3838963	M	MP:0031391	increased locomotor activity	Tg(Camk2a-tTA)1Mmay/0,Tg(tetO-DISC1*)1001Plet/0	involves: C57BL/6 * CBA * SJL	N	17848917
MGI:3838963	M	MP:0002557	abnormal social/conspecific interaction behavior	Tg(Camk2a-tTA)1Mmay/0,Tg(tetO-DISC1*)1001Plet/0	involves: C57BL/6 * CBA * SJL	N	17848917
MGI:3838974	M	MP:0004852	decreased testis weight	Eif2s2<Gt(XH413)Byg>/Eif2s2<+>	129-Eif2s2<Gt(XH413)Byg> Chr 19<MOLF/Ei>	N	19168544
MGI:3839124	M	MP:0001922	reduced male fertility	Tg(SV)427Bri/0	C57BL/6J-Tg(SV)427Bri	N	6327063
MGI:3839124	F	MP:0001926	female infertility	Tg(SV)427Bri/0	C57BL/6J-Tg(SV)427Bri	N	MGI:3839133
MGI:3839284	M	MP:0005376	homeostasis/metabolism phenotype	Hprt1<tm1(APOA5)Lap>/Y	involves: 129P2/OlaHsd * C57BL/6J	Y	17936576
MGI:3839285	M	MP:0005376	homeostasis/metabolism phenotype	Hprt1<tm2(APOA5)Lap>/Y	involves: 129P2/OlaHsd * C57BL/6J	Y	17936576
MGI:3839286	F	MP:0005376	homeostasis/metabolism phenotype	Hprt1<tm3(APOA5)Lap>/Hprt1<tm3(APOA5)Lap>	involves: 129P2/OlaHsd * C57BL/6J	Y	17936576
MGI:3839330	F	MP:0011125	decreased primary ovarian follicle number	Sohlh2<tm1Rajk>/Sohlh2<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	18753606
MGI:3839330	F	MP:0008871	abnormal ovarian follicle number	Sohlh2<tm1Rajk>/Sohlh2<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	18753606
MGI:3839330	F	MP:0005431	decreased oocyte number	Sohlh2<tm1Rajk>/Sohlh2<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	18753606
MGI:3839330	F	MP:0003357	impaired granulosa cell differentiation	Sohlh2<tm1Rajk>/Sohlh2<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	18753606
MGI:3839330	F	MP:0001926	female infertility	Sohlh2<tm1Rajk>/Sohlh2<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	18753606
MGI:3839330	F	MP:0004833	ovary atrophy	Sohlh2<tm1Rajk>/Sohlh2<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	18753606
MGI:3839539	M	MP:0001925	male infertility	Lpin1<fld-2J>/Lpin1<fld-2J>	C3H/HeJ-Lpin1<fld-2J>/J	N	11138012
MGI:3839562	M	MP:0004851	increased testis weight	Dkkl1<tm1Ducy>/Dkkl1<tm1Ducy>	involves: 129S7/SvEvBrd * C57BL/6J	N	18818293
MGI:3839562	M	MP:0030603	increased sperm number	Dkkl1<tm1Ducy>/Dkkl1<tm1Ducy>	involves: 129S7/SvEvBrd * C57BL/6J	N	18818293
MGI:3839562	M	MP:0008280	abnormal male germ cell apoptosis	Dkkl1<tm1Ducy>/Dkkl1<tm1Ducy>	involves: 129S7/SvEvBrd * C57BL/6J	N	18818293
MGI:3839772	M	MP:0008807	increased liver iron level	Hfe<tm1Gfn>/Hfe<tm1Gfn>	involves: 129P2/OlaHsd * C57BL/6	N	20976594
MGI:3839772	M	MP:0009346	decreased trabecular bone thickness	Hfe<tm1Gfn>/Hfe<tm1Gfn>	involves: 129P2/OlaHsd * C57BL/6	N	20976594
MGI:3839772	M	MP:0000130	abnormal trabecular bone morphology	Hfe<tm1Gfn>/Hfe<tm1Gfn>	involves: 129P2/OlaHsd * C57BL/6	N	20976594
MGI:3839772	M	MP:0010879	decreased trabecular bone volume	Hfe<tm1Gfn>/Hfe<tm1Gfn>	involves: 129P2/OlaHsd * C57BL/6	N	20976594
MGI:3839772	M	MP:0010869	decreased bone trabecula number	Hfe<tm1Gfn>/Hfe<tm1Gfn>	involves: 129P2/OlaHsd * C57BL/6	N	20976594
MGI:3839772	M	MP:0000066	osteoporosis	Hfe<tm1Gfn>/Hfe<tm1Gfn>	involves: 129P2/OlaHsd * C57BL/6	N	20976594
MGI:3839772	M	MP:0004984	increased osteoclast cell number	Hfe<tm1Gfn>/Hfe<tm1Gfn>	involves: 129P2/OlaHsd * C57BL/6	N	20976594
MGI:3839772	M	MP:0001260	increased body weight	Hfe<tm1Gfn>/Hfe<tm1Gfn>	involves: 129P2/OlaHsd * C57BL/6	N	20976594
MGI:3839772	M	MP:0001770	abnormal iron level	Hfe<tm1Gfn>/Hfe<tm1Gfn>	involves: 129P2/OlaHsd * C57BL/6	N	20976594
MGI:3839783	M	MP:0006262	increased testis tumor incidence	Men1<tm1.1Ctre>/Men1<+>	involves: 129S6/SvEvTac * C57BL/6	N	17409423
MGI:3839785	M	MP:0006262	increased testis tumor incidence	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	N	17409423
MGI:3839785	M	MP:0009592	increased Leydig cell tumor incidence	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	N	17409423
MGI:3839787	M	MP:0009381	abnormal prostate gland dorsolateral lobe morphology	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv	N	16014817
MGI:3839787	M	MP:0003607	abnormal prostate gland physiology	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv	N	16014817
MGI:3839788	M	MP:0006262	increased testis tumor incidence	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Men1<tm1.1Ctre>/Men1<+>	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	N	17409423
MGI:3839814	F	MP:0001556	increased circulating HDL cholesterol level	Hdlq15<129S1/SvImJ>/Hdlq15<129S1/SvImJ>,Hdlq60<C57BL/6J>/Hdlq60<C57BL/6J>	involves: 129S1/SvImJ * C57BL/6J	N	18772481
MGI:3839815	F	MP:0001556	increased circulating HDL cholesterol level	Hdlq15<129S1/SvImJ>/Hdlq15<129S1/SvImJ>,Hdlq60<129S1/SvImJ>/Hdlq60<C57BL/6J>	involves: 129S1/SvImJ * C57BL/6J	N	18772481
MGI:3839856	F	MP:0011121	decreased primordial ovarian follicle number	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839856	M	MP:0001145	abnormal male reproductive system morphology	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839856	F	MP:0001119	abnormal female reproductive system morphology	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839856	F	MP:0001134	absent corpus luteum	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839856	M	MP:0001147	small testis	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18755802
MGI:3839856	M	MP:0001925	male infertility	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18755802
MGI:3839856	F	MP:0031239	increased atretic ovarian follicle number	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839856	F	MP:0008984	vagina hypoplasia	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839856	M	MP:0004901	decreased male germ cell number	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18755802
MGI:3839856	F	MP:0001121	uterus hypoplasia	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839856	M	MP:0001154	seminiferous tubule degeneration	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18755802
MGI:3839856	F	MP:0001926	female infertility	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839856	F	MP:0011125	decreased primary ovarian follicle number	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839856	M	MP:0004852	decreased testis weight	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18755802
MGI:3839856	F	MP:0008256	abnormal myometrium morphology	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839856	F	MP:0001126	abnormal ovary morphology	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839856	M	MP:0009736	abnormal prostate gland branching morphogenesis	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18755802
MGI:3839856	F	MP:0002016	ovary cyst	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839856	M	MP:0003607	abnormal prostate gland physiology	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18755802
MGI:3839856	M	MP:0002687	oligozoospermia	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18755802
MGI:3839856	F	MP:0001129	impaired ovarian folliculogenesis	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839856	F	MP:0008868	abnormal granulosa cell morphology	Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129X1/SvJ * FVB/N	N	18953638
MGI:3839858	M	MP:0001154	seminiferous tubule degeneration	Esr1<tm1Ksk>/Esr1<tm1Ksk>	B6.129P2-Esr1<tm1Ksk>/J	N	18755802
MGI:3839858	M	MP:0002687	oligozoospermia	Esr1<tm1Ksk>/Esr1<tm1Ksk>	B6.129P2-Esr1<tm1Ksk>/J	N	18755802
MGI:3839897	M	MP:0001167	prostate gland epithelial hyperplasia	Tg(Pbsn-Cdc37)1Stp/0	involves: C57BL/6 * DBA/2 * ICR	N	10822368
MGI:3839897	M	MP:0001158	abnormal prostate gland morphology	Tg(Pbsn-Cdc37)1Stp/0	involves: C57BL/6 * DBA/2 * ICR	N	10822368
MGI:3839901	M	MP:0006262	increased testis tumor incidence	Tg(MMTV-CCND1)1Esmp/0	Not Specified	N	8208295
MGI:3839907	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-Cdc37)1Stp/0	involves: C57BL/6 * DBA/2 * FVB/N	N	10825210
MGI:3839907	F	MP:0006422	increased mammary adenoacanthoma incidence	Tg(MMTV-Cdc37)1Stp/0	involves: C57BL/6 * DBA/2 * FVB/N	N	10825210
MGI:3839907	F	MP:0012431	increased lymphoma incidence	Tg(MMTV-Cdc37)1Stp/0	involves: C57BL/6 * DBA/2 * FVB/N	N	10825210
MGI:3839907	M	MP:0000628	abnormal mammary gland development	Tg(MMTV-Cdc37)1Stp/0	involves: C57BL/6 * DBA/2 * FVB/N	N	10825210
MGI:3839907	F	MP:0002020	increased tumor incidence	Tg(MMTV-Cdc37)1Stp/0	involves: C57BL/6 * DBA/2 * FVB/N	N	10825210
MGI:3839908	M	MP:0000628	abnormal mammary gland development	Tg(MMTV-Cdc37)2Stp/0	involves: C57BL/6 * DBA/2 * FVB/N	N	10825210
MGI:3839908	F	MP:0002032	increased sarcoma incidence	Tg(MMTV-Cdc37)2Stp/0	involves: C57BL/6 * DBA/2 * FVB/N	N	10825210
MGI:3839908	F	MP:0012431	increased lymphoma incidence	Tg(MMTV-Cdc37)2Stp/0	involves: C57BL/6 * DBA/2 * FVB/N	N	10825210
MGI:3839908	F	MP:0006422	increased mammary adenoacanthoma incidence	Tg(MMTV-Cdc37)2Stp/0	involves: C57BL/6 * DBA/2 * FVB/N	N	10825210
MGI:3839908	F	MP:0002020	increased tumor incidence	Tg(MMTV-Cdc37)2Stp/0	involves: C57BL/6 * DBA/2 * FVB/N	N	10825210
MGI:3839909	F	MP:0000621	increased salivary adenocarcinoma incidence	Tg(MMTV-Cdc37)1Stp/0,Tg(MMTV-Myc)141-3Led/0	involves: C57BL/6 * CD-1 * DBA/2 * FVB/N	N	10825210
MGI:3839909	M	MP:0009592	increased Leydig cell tumor incidence	Tg(MMTV-Cdc37)1Stp/0,Tg(MMTV-Myc)141-3Led/0	involves: C57BL/6 * CD-1 * DBA/2 * FVB/N	N	10825210
MGI:3839909	F	MP:0002020	increased tumor incidence	Tg(MMTV-Cdc37)1Stp/0,Tg(MMTV-Myc)141-3Led/0	involves: C57BL/6 * CD-1 * DBA/2 * FVB/N	N	10825210
MGI:3839909	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-Cdc37)1Stp/0,Tg(MMTV-Myc)141-3Led/0	involves: C57BL/6 * CD-1 * DBA/2 * FVB/N	N	10825210
MGI:3839909	M	MP:0001152	increased Leydig cell number	Tg(MMTV-Cdc37)1Stp/0,Tg(MMTV-Myc)141-3Led/0	involves: C57BL/6 * CD-1 * DBA/2 * FVB/N	N	10825210
MGI:3839909	F	MP:0010299	increased mammary gland tumor incidence	Tg(MMTV-Cdc37)1Stp/0,Tg(MMTV-Myc)141-3Led/0	involves: C57BL/6 * CD-1 * DBA/2 * FVB/N	N	10825210
MGI:3839909	F	MP:0012431	increased lymphoma incidence	Tg(MMTV-Cdc37)1Stp/0,Tg(MMTV-Myc)141-3Led/0	involves: C57BL/6 * CD-1 * DBA/2 * FVB/N	N	10825210
MGI:3839910	F	MP:0010299	increased mammary gland tumor incidence	Tg(MMTV-CCND1)1Esmp/0,Tg(MMTV-Cdc37)1Stp/0	involves: C57BL/6 * DBA/2 * FVB/N	N	10825210
MGI:3839910	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-CCND1)1Esmp/0,Tg(MMTV-Cdc37)1Stp/0	involves: C57BL/6 * DBA/2 * FVB/N	N	10825210
MGI:3839911	F	MP:0002023	increased B cell derived lymphoma incidence	Tg(MMTV-Myc)141-3Led/0	involves: C57BL/6J * CD-1	N	10825210
MGI:3839911	F	MP:0002020	increased tumor incidence	Tg(MMTV-Myc)141-3Led/0	involves: C57BL/6J * CD-1	N	10825210
MGI:3839911	M	MP:0001152	increased Leydig cell number	Tg(MMTV-Myc)141-3Led/0	involves: C57BL/6J * CD-1	N	10825210
MGI:3840076	M	MP:0001157	small seminal vesicle	Ptch1<mes>/Ptch1<mes>	B6C3Fe a/a-Ptch1<mes>	N	8830098
MGI:3840076	M	MP:0001156	abnormal spermatogenesis	Ptch1<mes>/Ptch1<mes>	B6C3Fe a/a-Ptch1<mes>	N	8830098
MGI:3840076	F	MP:0001926	female infertility	Ptch1<mes>/Ptch1<mes>	B6C3Fe a/a-Ptch1<mes>	N	MGI:72837
MGI:3840076	M	MP:0002286	cryptorchism	Ptch1<mes>/Ptch1<mes>	B6C3Fe a/a-Ptch1<mes>	N	MGI:72837
MGI:3840076	M	MP:0002716	small male preputial gland	Ptch1<mes>/Ptch1<mes>	B6C3Fe a/a-Ptch1<mes>	N	8830098
MGI:3840076	M	MP:0001925	male infertility	Ptch1<mes>/Ptch1<mes>	B6C3Fe a/a-Ptch1<mes>	N	MGI:72837
MGI:3840234	M	MP:0001156	abnormal spermatogenesis	Kdm3a<tm1.1Yzha>/Kdm3a<tm1.1Yzha>	B6.129P2-Kdm3a<tm1.1Yzha>	N	19194461
MGI:3840259	M	MP:0001925	male infertility	Ndc1<sks>/Ndc1<sks>	involves: A/J	N	3220432
MGI:3840259	M	MP:0001147	small testis	Ndc1<sks>/Ndc1<sks>	involves: A/J	N	3220432
MGI:3840259	M	MP:0008261	arrest of male meiosis	Ndc1<sks>/Ndc1<sks>	involves: A/J	N	3220432
MGI:3840259	F	MP:0001926	female infertility	Ndc1<sks>/Ndc1<sks>	involves: A/J	N	3220432
MGI:3840259	M	MP:0005169	abnormal male meiosis	Ndc1<sks>/Ndc1<sks>	involves: A/J	N	3220432
MGI:3840273	M	MP:0003205	testicular atrophy	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	N	8653789
MGI:3840273	M	MP:0001152	increased Leydig cell number	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	N	8653789
MGI:3840273	M	MP:0001154	seminiferous tubule degeneration	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	N	8653789
MGI:3840353	F	MP:0004898	uterine hemorrhage	E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	N	9537419
MGI:3840514	F	MP:0009661	abnormal pregnancy	Clock<m1Jt>/Clock<m1Jt>	involves: C57BL/6	N	15296754
MGI:3840514	F	MP:0002907	abnormal parturition	Clock<m1Jt>/Clock<m1Jt>	involves: C57BL/6	N	15296754
MGI:3840514	F	MP:0009015	short proestrus	Clock<m1Jt>/Clock<m1Jt>	involves: C57BL/6	N	15296754
MGI:3840514	F	MP:0009006	prolonged estrous cycle	Clock<m1Jt>/Clock<m1Jt>	involves: C57BL/6	N	15296754
MGI:3840514	F	MP:0009017	prolonged estrus	Clock<m1Jt>/Clock<m1Jt>	involves: C57BL/6	N	15296754
MGI:3840546	M	MP:0001402	decreased locomotor activity	Mecp2<tm2.1Jae>/Y	involves: 129/Sv * C57BL/6	N	19225110
MGI:3840546	M	MP:0001260	increased body weight	Mecp2<tm2.1Jae>/Y	involves: 129/Sv * C57BL/6	N	19225110
MGI:3840547	M	MP:0001399	hyperactivity	Mecp2<tm3.1Jae>/Y	involves: 129/Sv * C57BL/6	N	19225110
MGI:3840547	M	MP:0002176	increased brain weight	Mecp2<tm3.1Jae>/Y	involves: 129/Sv * C57BL/6	N	19225110
MGI:3840565	M	MP:0005159	azoospermia	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	N	19247432
MGI:3840565	M	MP:0014052	increased male germ cell apoptosis	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	N	19247432
MGI:3840565	M	MP:0001147	small testis	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	N	19247432
MGI:3840565	M	MP:0001925	male infertility	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	N	19247432
MGI:3840565	F	MP:0001926	female infertility	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	N	19247432
MGI:3840565	F	MP:0002682	decreased mature ovarian follicle number	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	N	19247432
MGI:3840565	F	MP:0001127	small ovary	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	N	19247432
MGI:3840565	M	MP:0008261	arrest of male meiosis	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	N	19247432
MGI:3840610	M	MP:0003205	testicular atrophy	E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm1Lees>/E2f3<+>	involves: 129S2/SvPas	N	11909960
MGI:3840644	F	MP:0003253	dilated bile duct	Abcb4<tm1Bor>/Abcb4<tm1Bor>	FVB.129P2-Abcb4<tm1Bor>/J	N	14752830
MGI:3840654	F	MP:0001260	increased body weight	Ar<Tfm-Jms>/Ar<Tfm-Jms>	involves: C57BL/6JJms	N	7967466
MGI:3840654	F	MP:0001926	female infertility	Ar<Tfm-Jms>/Ar<Tfm-Jms>	involves: C57BL/6JJms	N	7967466
MGI:3840676	F	MP:0012008	delayed parturition	Dscam<tm1.1Kzy>/Dscam<+>	B6.129P2-Dscam<tm1.1Kzy>	N	19261893
MGI:3840688	F	MP:0003568	uterus atresia	Cdkn1c<tm1.1(Cdkn1b*)Kei>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	N	19276117
MGI:3840688	F	MP:0004894	uterus atrophy	Cdkn1c<tm1.1(Cdkn1b*)Kei>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	N	19276117
MGI:3840689	F	MP:0003568	uterus atresia	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	N	19276117
MGI:3840689	F	MP:0004894	uterus atrophy	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	N	19276117
MGI:3840844	M	MP:0001922	reduced male fertility	Hoxd12<tm2Ddu>/Hoxd12<tm2Ddu>,Hoxd13<tm2Ddu>/Hoxd13<tm2Ddu>	involves: 129S2/SvPas	N	9659925
MGI:3841005	M	MP:0003545	increased alcohol consumption	Ccr2<tm1Mae>/Ccr2<tm1Mae>	B6.129P2-Ccr2<tm1Mae>	N	16105698
MGI:3841093	M	MP:0001925	male infertility	Cby1<tm1Ktkm>/Cby1<tm1Ktkm>	B6.129-Cby1<tm1Ktkm>	N	19364920
MGI:3841153	F	MP:0002906	increased susceptibility to pharmacologically induced seizures	Gdi1<tm1Ytk>/Gdi1<tm1Ytk>	either: (involves: 129X1/SvJ * C57BL/6) or (involves: 129X1/SvJ * C57BL/6 * DBA/2)	N	11027356
MGI:3841153	F	MP:0002919	enhanced paired-pulse facilitation	Gdi1<tm1Ytk>/Gdi1<tm1Ytk>	either: (involves: 129X1/SvJ * C57BL/6) or (involves: 129X1/SvJ * C57BL/6 * DBA/2)	N	11027356
MGI:3841153	F	MP:0002910	abnormal excitatory postsynaptic currents	Gdi1<tm1Ytk>/Gdi1<tm1Ytk>	either: (involves: 129X1/SvJ * C57BL/6) or (involves: 129X1/SvJ * C57BL/6 * DBA/2)	N	11027356
MGI:3841394	F	MP:0002169	no abnormal phenotype detected	Ar<tm1Rax>/Ar<tm1Rax>	involves: 129S/SvEv * C57BL/6J	N	15294140
MGI:3841395	M	MP:0002169	no abnormal phenotype detected	Ar<tm1Rax>/Y	involves: 129S/SvEv * C57BL/6J	N	15294140
MGI:3841489	M	MP:0005669	increased circulating leptin level	Htr2c<tm1Jke>/Y	B6.129-Htr2c<tm1Jke>	N	19038216
MGI:3841489	M	MP:0005458	increased percent body fat/body weight	Htr2c<tm1Jke>/Y	B6.129-Htr2c<tm1Jke>	N	19038216
MGI:3841489	M	MP:0001399	hyperactivity	Htr2c<tm1Jke>/Y	B6.129-Htr2c<tm1Jke>	N	19038216
MGI:3841489	M	MP:0003997	tonic-clonic seizures	Htr2c<tm1Jke>/Y	B6.129-Htr2c<tm1Jke>	N	19038216
MGI:3841489	M	MP:0005658	increased susceptibility to diet-induced obesity	Htr2c<tm1Jke>/Y	B6.129-Htr2c<tm1Jke>	N	19038216
MGI:3841489	M	MP:0009747	impaired behavioral response to xenobiotic	Htr2c<tm1Jke>/Y	B6.129-Htr2c<tm1Jke>	N	19038216
MGI:3841489	M	MP:0001433	polyphagia	Htr2c<tm1Jke>/Y	B6.129-Htr2c<tm1Jke>	N	19038216
MGI:3841489	M	MP:0002083	premature death	Htr2c<tm1Jke>/Y	B6.129-Htr2c<tm1Jke>	N	19038216
MGI:3841489	M	MP:0000008	increased white adipose tissue amount	Htr2c<tm1Jke>/Y	B6.129-Htr2c<tm1Jke>	N	19038216
MGI:3841489	M	MP:0003961	decreased lean body mass	Htr2c<tm1Jke>/Y	B6.129-Htr2c<tm1Jke>	N	19038216
MGI:3841490	M	MP:0003997	tonic-clonic seizures	Htr2c<tm1Jke>/Y,Tg(Pomc1-cre)16Lowl/0	B6.Cg-Htr2c<tm1Jke> Tg(Pomc1-cre)16Lowl	N	19038216
MGI:3841490	M	MP:0005376	homeostasis/metabolism phenotype	Htr2c<tm1Jke>/Y,Tg(Pomc1-cre)16Lowl/0	B6.Cg-Htr2c<tm1Jke> Tg(Pomc1-cre)16Lowl	Y	19038216
MGI:3841490	M	MP:0005375	adipose tissue phenotype	Htr2c<tm1Jke>/Y,Tg(Pomc1-cre)16Lowl/0	B6.Cg-Htr2c<tm1Jke> Tg(Pomc1-cre)16Lowl	Y	19038216
MGI:3841490	M	MP:0005386	behavior/neurological phenotype	Htr2c<tm1Jke>/Y,Tg(Pomc1-cre)16Lowl/0	B6.Cg-Htr2c<tm1Jke> Tg(Pomc1-cre)16Lowl	Y	19038216
MGI:3841490	M	MP:0005378	growth/size/body region phenotype	Htr2c<tm1Jke>/Y,Tg(Pomc1-cre)16Lowl/0	B6.Cg-Htr2c<tm1Jke> Tg(Pomc1-cre)16Lowl	Y	19038216
MGI:3841490	M	MP:0002083	premature death	Htr2c<tm1Jke>/Y,Tg(Pomc1-cre)16Lowl/0	B6.Cg-Htr2c<tm1Jke> Tg(Pomc1-cre)16Lowl	N	19038216
MGI:3841558	F	MP:0001927	abnormal estrous cycle	Tacr3<tm1Jasi>/Tacr3<tm1Jasi>	involves: 129P2/OlaHsd * C57BL/6	N	22253416
MGI:3841558	F	MP:0004905	decreased uterus weight	Tacr3<tm1Jasi>/Tacr3<tm1Jasi>	involves: 129P2/OlaHsd * C57BL/6	N	22253416
MGI:3841558	M	MP:0001147	small testis	Tacr3<tm1Jasi>/Tacr3<tm1Jasi>	involves: 129P2/OlaHsd * C57BL/6	N	22253416
MGI:3841558	F	MP:0005389	reproductive system phenotype	Tacr3<tm1Jasi>/Tacr3<tm1Jasi>	involves: 129P2/OlaHsd * C57BL/6	Y	25574869
MGI:3841558	F	MP:0001262	decreased body weight	Tacr3<tm1Jasi>/Tacr3<tm1Jasi>	involves: 129P2/OlaHsd * C57BL/6	N	22253416
MGI:3841558	F	MP:0009011	prolonged diestrus	Tacr3<tm1Jasi>/Tacr3<tm1Jasi>	involves: 129P2/OlaHsd * C57BL/6	N	22253416
MGI:3841558	F	MP:0001923	reduced female fertility	Tacr3<tm1Jasi>/Tacr3<tm1Jasi>	involves: 129P2/OlaHsd * C57BL/6	N	22253416
MGI:3841558	M	MP:0002790	decreased circulating follicle stimulating hormone level	Tacr3<tm1Jasi>/Tacr3<tm1Jasi>	involves: 129P2/OlaHsd * C57BL/6	N	22253416
MGI:3841621	F	MP:0011091	prenatal lethality, complete penetrance	Ogt<tm1Gwh>/Ogt<tm1Gwh>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ	N	10801981
MGI:3841621	F	MP:0001926	female infertility	Ogt<tm1Gwh>/Ogt<tm1Gwh>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ	N	14749383
MGI:3841622	F	MP:0011091	prenatal lethality, complete penetrance	Ogt<tm1Gwh>/Ogt<+>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ	N	10801981
MGI:3841623	M	MP:0011091	prenatal lethality, complete penetrance	Ogt<tm1Gwh>/Y,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ	N	10801981
MGI:3841624	M	MP:0000313	abnormal cell death	Ogt<tm1Gwh>/Y	involves: 129S1/Sv * 129X1/SvJ	N	14749383
MGI:3841624	M	MP:0000313	abnormal cell death	Ogt<tm1Gwh>/Y	involves: 129S1/Sv * 129X1/SvJ	N	10801981
MGI:3841624	M	MP:0000352	decreased cell proliferation	Ogt<tm1Gwh>/Y	involves: 129S1/Sv * 129X1/SvJ	N	14749383
MGI:3841625	M	MP:0005092	decreased double-positive T cell number	Ogt<tm1Gwh>/Y,Tg(Lck-cre)548Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841625	M	MP:0000715	decreased thymocyte number	Ogt<tm1Gwh>/Y,Tg(Lck-cre)548Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841625	M	MP:0006413	increased T cell apoptosis	Ogt<tm1Gwh>/Y,Tg(Lck-cre)548Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841625	M	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Ogt<tm1Gwh>/Y,Tg(Lck-cre)548Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841625	M	MP:0005018	decreased T cell number	Ogt<tm1Gwh>/Y,Tg(Lck-cre)548Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841625	M	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Ogt<tm1Gwh>/Y,Tg(Lck-cre)548Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841626	M	MP:0001436	abnormal suckling behavior	Ogt<tm1Gwh>/Y,Tg(Syn1-cre)671Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841626	M	MP:0011101	prenatal lethality, incomplete penetrance	Ogt<tm1Gwh>/Y,Tg(Syn1-cre)671Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841626	M	MP:0001392	abnormal locomotor behavior	Ogt<tm1Gwh>/Y,Tg(Syn1-cre)671Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841626	M	MP:0004200	decreased fetal size	Ogt<tm1Gwh>/Y,Tg(Syn1-cre)671Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841626	M	MP:0011085	postnatal lethality, complete penetrance	Ogt<tm1Gwh>/Y,Tg(Syn1-cre)671Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841627	F	MP:0004200	decreased fetal size	Ogt<tm1Gwh>/Ogt<tm1Gwh>,Tg(Syn1-cre)671Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841627	F	MP:0001436	abnormal suckling behavior	Ogt<tm1Gwh>/Ogt<tm1Gwh>,Tg(Syn1-cre)671Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841627	F	MP:0001392	abnormal locomotor behavior	Ogt<tm1Gwh>/Ogt<tm1Gwh>,Tg(Syn1-cre)671Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841627	F	MP:0011085	postnatal lethality, complete penetrance	Ogt<tm1Gwh>/Ogt<tm1Gwh>,Tg(Syn1-cre)671Jxm/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	14749383
MGI:3841629	F	MP:0002169	no abnormal phenotype detected	Ogt<tm1Gwh>/Ogt<+>,Tg(Prm-cre)58Og/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	14749383
MGI:3841697	M	MP:0004543	abnormal sperm physiology	Aqp7<tm1Nlsn>/Aqp7<tm1Nlsn>	involves: 129S1/Sv * C57BL/6N	N	18829704
MGI:3841959	F	MP:0009082	uterus cyst	Cyp11b1<tm1Chjk>/Cyp11b1<tm1Chjk>	involves: 129P2/OlaHsd * C57BL/6J	N	19029289
MGI:3841959	F	MP:0004906	enlarged uterus	Cyp11b1<tm1Chjk>/Cyp11b1<tm1Chjk>	involves: 129P2/OlaHsd * C57BL/6J	N	19029289
MGI:3841959	F	MP:0001926	female infertility	Cyp11b1<tm1Chjk>/Cyp11b1<tm1Chjk>	involves: 129P2/OlaHsd * C57BL/6J	N	19029289
MGI:3841959	F	MP:0009092	endometrium hyperplasia	Cyp11b1<tm1Chjk>/Cyp11b1<tm1Chjk>	involves: 129P2/OlaHsd * C57BL/6J	N	19029289
MGI:3841959	F	MP:0001134	absent corpus luteum	Cyp11b1<tm1Chjk>/Cyp11b1<tm1Chjk>	involves: 129P2/OlaHsd * C57BL/6J	N	19029289
MGI:3841959	F	MP:0009221	uterus adenomyosis	Cyp11b1<tm1Chjk>/Cyp11b1<tm1Chjk>	involves: 129P2/OlaHsd * C57BL/6J	N	19029289
MGI:3841997	M	MP:0000396	increased curvature of hairs	Eda<Ta-J>/Y	involves: 129	N	MGI:63195
MGI:3841997	M	MP:0000416	sparse hair	Eda<Ta-J>/Y	involves: 129	N	MGI:63195
MGI:3841998	F	MP:0000418	focal hair loss	Eda<Ta-J>/Eda<+>	involves: 129	N	MGI:63195
MGI:3841998	F	MP:0000396	increased curvature of hairs	Eda<Ta-J>/Eda<+>	involves: 129	N	MGI:63195
MGI:3841998	F	MP:0000416	sparse hair	Eda<Ta-J>/Eda<+>	involves: 129	N	MGI:63195
MGI:3842168	F	MP:0009652	abnormal palatal rugae morphology	Eda<Ta-5J>/Eda<+>	C3H/HeJ-Eda<Ta-5J>/J	N	18028050
MGI:3842172	F	MP:0009652	abnormal palatal rugae morphology	Eda<Ta>/Eda<+>	C57BL/6J-A<w-J>-Eda<Ta> +/+ Ar<Tfm>/J	N	18028050
MGI:3842174	F	MP:0009652	abnormal palatal rugae morphology	Eda<Ta>/Eda<+>	B6CBACa A<w-J>/A-Eda<Ta>/J-XO	N	18028050
MGI:3842175	M	MP:0009652	abnormal palatal rugae morphology	Eda<Ta>/Y	B6CBACa A<w-J>/A-Eda<Ta>/J-XO	N	18028050
MGI:3842217	F	MP:0009088	thin uterine horn	Wwox<tm1Ria>/Wwox<tm1Ria>	involves: 129X1/SvJ * C57BL/6J	N	18974271
MGI:3842217	M	MP:0001940	testis hypoplasia	Wwox<tm1Ria>/Wwox<tm1Ria>	involves: 129X1/SvJ * C57BL/6J	N	18974271
MGI:3842217	M	MP:0005536	decreased Leydig cell number	Wwox<tm1Ria>/Wwox<tm1Ria>	involves: 129X1/SvJ * C57BL/6J	N	18974271
MGI:3842217	M	MP:0001153	small seminiferous tubules	Wwox<tm1Ria>/Wwox<tm1Ria>	involves: 129X1/SvJ * C57BL/6J	N	18974271
MGI:3842217	F	MP:0009362	abnormal primary ovarian follicle morphology	Wwox<tm1Ria>/Wwox<tm1Ria>	involves: 129X1/SvJ * C57BL/6J	N	18974271
MGI:3842217	F	MP:0009370	decreased theca cell number	Wwox<tm1Ria>/Wwox<tm1Ria>	involves: 129X1/SvJ * C57BL/6J	N	18974271
MGI:3842217	M	MP:0001147	small testis	Wwox<tm1Ria>/Wwox<tm1Ria>	involves: 129X1/SvJ * C57BL/6J	N	18974271
MGI:3842217	F	MP:0001127	small ovary	Wwox<tm1Ria>/Wwox<tm1Ria>	involves: 129X1/SvJ * C57BL/6J	N	18974271
MGI:3842379	F	MP:0009221	uterus adenomyosis	Kras<tm4Tyj>/Kras<+>	involves: 129S4/SvJae	N	19841240
MGI:3842676	M	MP:0001925	male infertility	Cdkn2a<tm3(cre)Cjs>/Cdkn2a<+>	involves: 129S1/Sv * C57BL/6	N	19339492
MGI:3842791	M	MP:0011339	abnormal glomerular mesangium morphology	Tg(Ckm-IGF1R*K1003R)1Dlr/0	FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	N	24598803
MGI:3842791	M	MP:0003917	increased kidney weight	Tg(Ckm-IGF1R*K1003R)1Dlr/0	FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	N	24598803
MGI:3842791	M	MP:0011753	decreased podocyte number	Tg(Ckm-IGF1R*K1003R)1Dlr/0	FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	N	24598803
MGI:3842791	M	MP:0005325	abnormal renal glomerulus morphology	Tg(Ckm-IGF1R*K1003R)1Dlr/0	FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	N	24598803
MGI:3842791	M	MP:0005527	increased renal glomerular filtration rate	Tg(Ckm-IGF1R*K1003R)1Dlr/0	FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	N	24598803
MGI:3842791	M	MP:0002871	albuminuria	Tg(Ckm-IGF1R*K1003R)1Dlr/0	FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	N	24598803
MGI:3842791	M	MP:0008489	slow postnatal weight gain	Tg(Ckm-IGF1R*K1003R)1Dlr/0	FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	N	24598803
MGI:3842791	M	MP:0008140	podocyte foot process effacement	Tg(Ckm-IGF1R*K1003R)1Dlr/0	FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	N	24598803
MGI:3842791	M	MP:0005553	increased circulating creatinine level	Tg(Ckm-IGF1R*K1003R)1Dlr/0	FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	N	24598803
MGI:3842791	M	MP:0002842	increased systemic arterial blood pressure	Tg(Ckm-IGF1R*K1003R)1Dlr/0	FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	N	24598803
MGI:3842791	M	MP:0001559	hyperglycemia	Tg(Ckm-IGF1R*K1003R)1Dlr/0	FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	N	24598803
MGI:3842791	M	MP:0005178	increased circulating cholesterol level	Tg(Ckm-IGF1R*K1003R)1Dlr/0	FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	N	24598803
MGI:3842791	M	MP:0011409	increased renal glomerulus basement membrane thickness	Tg(Ckm-IGF1R*K1003R)1Dlr/0	FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	N	24598803
MGI:3843449	M	MP:0009237	kinked sperm flagellum	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0002687	oligozoospermia	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0008898	abnormal acrosome morphology	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0009230	abnormal sperm head morphology	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0002675	asthenozoospermia	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0001155	arrest of spermatogenesis	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0009231	detached acrosome	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0002686	globozoospermia	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0004852	decreased testis weight	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0009232	abnormal sperm nucleus morphology	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0008545	absent sperm flagellum	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0004901	decreased male germ cell number	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0001925	male infertility	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843449	M	MP:0008280	abnormal male germ cell apoptosis	Septin12<tm1.1Plk>/Septin12<+>	chimera involves: 129/Sv * C57BL/6	N	19359518
MGI:3843497	F	MP:0000627	abnormal mammary gland morphology	Cav1<tm1Mls>/Cav1<tm1Mls>	involves: 129/Sv * C57BL/6 * FVB/N * SJL	N	19342371
MGI:3843773	M	MP:0002675	asthenozoospermia	Tekt3<tm1Zuk>/Tekt3<tm1Zuk>	either: 129S7/SvEvBrd-Tekt3<tm1Zuk> or (involves: 129S7/SvEvBrd * C57BL/6J)	N	18951373
MGI:3843773	M	MP:0009243	hairpin sperm flagellum	Tekt3<tm1Zuk>/Tekt3<tm1Zuk>	either: 129S7/SvEvBrd-Tekt3<tm1Zuk> or (involves: 129S7/SvEvBrd * C57BL/6J)	N	18951373
MGI:3843774	M	MP:0002675	asthenozoospermia	Tekt3<tm1Zuk>/Tekt3<tm1Zuk>,Tekt4<tm1Zuk>/Tekt4<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	18951373
MGI:3843774	M	MP:0001922	reduced male fertility	Tekt3<tm1Zuk>/Tekt3<tm1Zuk>,Tekt4<tm1Zuk>/Tekt4<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	18951373
MGI:3843785	F	MP:0000627	abnormal mammary gland morphology	Foxb1<tm1Lby>/Foxb1<tm1Lby>	involves: 129S6/SvEvTac * Black Swiss	N	11170346
MGI:3843796	F	MP:0000627	abnormal mammary gland morphology	Foxb1<tm1Lby>/Foxb1<tm1Lby>	B6.129S6-Foxb1<tm1Lby>	N	11170346
MGI:3843796	F	MP:0009504	abnormal mammary gland epithelium morphology	Foxb1<tm1Lby>/Foxb1<tm1Lby>	B6.129S6-Foxb1<tm1Lby>	N	11170346
MGI:3843796	F	MP:0013718	galactostasis	Foxb1<tm1Lby>/Foxb1<tm1Lby>	B6.129S6-Foxb1<tm1Lby>	N	11170346
MGI:3843796	F	MP:0009506	abnormal mammary gland alveolus morphology	Foxb1<tm1Lby>/Foxb1<tm1Lby>	B6.129S6-Foxb1<tm1Lby>	N	11170346
MGI:3843796	F	MP:0009505	abnormal mammary gland lobule morphology	Foxb1<tm1Lby>/Foxb1<tm1Lby>	B6.129S6-Foxb1<tm1Lby>	N	11170346
MGI:3843799	F	MP:0013718	galactostasis	Foxb1<tm1Lby>/Foxb1<tm1Lby>	129S6/SvEvTac-Foxb1<tm1Lby>	N	11170346
MGI:3843800	F	MP:0001926	female infertility	Kit<W-55J>/Kit<W-55J>	C57BL/6J-Kit<W-55J>/J	N	1692559
MGI:3843800	M	MP:0001925	male infertility	Kit<W-55J>/Kit<W-55J>	C57BL/6J-Kit<W-55J>/J	N	1692559
MGI:3843814	F	MP:0001698	decreased embryo size	Pdha1<tm1.1Ptl>/Pdha1<tm1.1Ptl>	involves: 129P2/OlaHsd * FVB/N	N	11708858
MGI:3843814	F	MP:0003984	embryonic growth retardation	Pdha1<tm1.1Ptl>/Pdha1<tm1.1Ptl>	involves: 129P2/OlaHsd * FVB/N	N	11708858
MGI:3843814	F	MP:0011092	embryonic lethality, complete penetrance	Pdha1<tm1.1Ptl>/Pdha1<tm1.1Ptl>	involves: 129P2/OlaHsd * FVB/N	N	11708858
MGI:3843815	M	MP:0003984	embryonic growth retardation	Pdha1<tm1.1Ptl>/Y	involves: 129P2/OlaHsd * FVB/N	N	11708858
MGI:3843815	M	MP:0011092	embryonic lethality, complete penetrance	Pdha1<tm1.1Ptl>/Y	involves: 129P2/OlaHsd * FVB/N	N	11708858
MGI:3843815	M	MP:0001698	decreased embryo size	Pdha1<tm1.1Ptl>/Y	involves: 129P2/OlaHsd * FVB/N	N	11708858
MGI:3843822	M	MP:0011091	prenatal lethality, complete penetrance	Pdha1<tm1Ptl>/Y,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0005237	abnormal olfactory tract morphology	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0000852	small cerebellum	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0004079	abnormal putamen morphology	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0000781	decreased corpus callosum size	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0009969	abnormal cerebral cortex pyramidal cell morphology	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0000832	abnormal thalamus morphology	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0000880	decreased Purkinje cell number	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0011101	prenatal lethality, incomplete penetrance	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0020554	decreased stria medullaris size	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0008026	abnormal brain white matter morphology	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0008931	abnormal paraventricular thalamic nucleus morphology	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0000886	abnormal cerebellar granule layer morphology	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0000889	abnormal cerebellar molecular layer	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0009979	abnormal cerebellum deep nucleus morphology	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0002175	decreased brain weight	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0009976	abnormal cerebellar peduncle morphology	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843824	F	MP:0008547	abnormal neocortex morphology	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	15569252
MGI:3843832	F	MP:0000402	abnormal zigzag hair morphology	Ophn1<Wtgr>/Ophn1<+>	D2(B6)-Ophn1<Wtgr>/EiGrsrJ	N	MGI:3718087
MGI:3843832	F	MP:0000410	waved hair	Ophn1<Wtgr>/Ophn1<+>	D2(B6)-Ophn1<Wtgr>/EiGrsrJ	N	MGI:3718087
MGI:3843832	F	MP:0001935	decreased litter size	Ophn1<Wtgr>/Ophn1<+>	D2(B6)-Ophn1<Wtgr>/EiGrsrJ	N	MGI:3718087
MGI:3843832	F	MP:0010231	transverse fur striping	Ophn1<Wtgr>/Ophn1<+>	D2(B6)-Ophn1<Wtgr>/EiGrsrJ	N	MGI:3718087
MGI:3843832	F	MP:0001265	decreased body size	Ophn1<Wtgr>/Ophn1<+>	D2(B6)-Ophn1<Wtgr>/EiGrsrJ	N	MGI:3718087
MGI:3843832	F	MP:0001274	curly vibrissae	Ophn1<Wtgr>/Ophn1<+>	D2(B6)-Ophn1<Wtgr>/EiGrsrJ	N	MGI:3718087
MGI:3843840	F	MP:0001926	female infertility	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Zp3-cre)93Knw/0	involves: 129P2/OlaHsd * C57BL/6J	N	17314311
MGI:3843840	F	MP:0014447	impaired spindle assembly in female meiosis	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Zp3-cre)93Knw/0	involves: 129P2/OlaHsd * C57BL/6J	N	17314311
MGI:3843840	F	MP:0012736	abnormal polar body morphology	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Zp3-cre)93Knw/0	involves: 129P2/OlaHsd * C57BL/6J	N	17314311
MGI:3843840	F	MP:0001125	abnormal oocyte morphology	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Zp3-cre)93Knw/0	involves: 129P2/OlaHsd * C57BL/6J	N	17314311
MGI:3843840	F	MP:0005168	abnormal female meiosis	Pdha1<tm1Ptl>/Pdha1<tm1Ptl>,Tg(Zp3-cre)93Knw/0	involves: 129P2/OlaHsd * C57BL/6J	N	17314311
MGI:3843870	M	MP:0002083	premature death	Pdha1<tm1Ptl>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843870	M	MP:0002625	heart left ventricle hypertrophy	Pdha1<tm1Ptl>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843870	M	MP:0002079	increased circulating insulin level	Pdha1<tm1Ptl>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843870	M	MP:0001260	increased body weight	Pdha1<tm1Ptl>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843870	M	MP:0005140	decreased cardiac muscle contractility	Pdha1<tm1Ptl>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843870	M	MP:0004564	increased myocardial fiber size	Pdha1<tm1Ptl>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843870	M	MP:0003921	abnormal heart left ventricle morphology	Pdha1<tm1Ptl>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843870	M	MP:0002833	increased heart weight	Pdha1<tm1Ptl>/Y,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843872	F	MP:0002079	increased circulating insulin level	Pdha1<tm1Ptl>/Pdha1<+>,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843872	F	MP:0002833	increased heart weight	Pdha1<tm1Ptl>/Pdha1<+>,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843872	F	MP:0003921	abnormal heart left ventricle morphology	Pdha1<tm1Ptl>/Pdha1<+>,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843872	F	MP:0001260	increased body weight	Pdha1<tm1Ptl>/Pdha1<+>,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843872	F	MP:0004564	increased myocardial fiber size	Pdha1<tm1Ptl>/Pdha1<+>,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843872	F	MP:0005140	decreased cardiac muscle contractility	Pdha1<tm1Ptl>/Pdha1<+>,Tg(Ckmm-cre)5Khn/0	involves: 129P2/OlaHsd * FVB	N	18586888
MGI:3843955	M	MP:0002675	asthenozoospermia	Ophn1<Wtgr>/Y	D2(B6)-Ophn1<Wtgr>/EiGrsrJ	N	MGI:3718087
MGI:3843955	M	MP:0011110	preweaning lethality, incomplete penetrance	Ophn1<Wtgr>/Y	D2(B6)-Ophn1<Wtgr>/EiGrsrJ	N	MGI:3718087
MGI:3844244	M	MP:0001925	male infertility	Grid2<ho-cpr>/Grid2<ho-cpr>	involves: C57BL/10J * DBA/2J	N	MGI:62172
MGI:3844255	F	MP:0013716	hypolactation	Pxmp2<tm1Jkh>/Pxmp2<tm1Jkh>	B6.129X1-Pxmp2<tm1Jkh>	N	19352492
MGI:3844255	F	MP:0006269	abnormal mammary gland growth during pregnancy	Pxmp2<tm1Jkh>/Pxmp2<tm1Jkh>	B6.129X1-Pxmp2<tm1Jkh>	N	19352492
MGI:3844255	F	MP:0001119	abnormal female reproductive system morphology	Pxmp2<tm1Jkh>/Pxmp2<tm1Jkh>	B6.129X1-Pxmp2<tm1Jkh>	N	19352492
MGI:3844341	M	MP:0001925	male infertility	Hoxd9<tm1Emca>/Hoxd9<tm1Emca>,Hoxd10<tm1Emca>/Hoxd10<tm1Emca>	involves: 129S7/SvEvBrd * C57BL/6	N	10642795
MGI:3844352	M	MP:0003996	clonic seizures	Arx<tm1Gldn>/Y,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	N	19439424
MGI:3844352	M	MP:0004994	abnormal brain wave pattern	Arx<tm1Gldn>/Y,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	N	19439424
MGI:3844352	M	MP:0003997	tonic-clonic seizures	Arx<tm1Gldn>/Y,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	N	19439424
MGI:3844352	M	MP:0004101	abnormal brain interneuron morphology	Arx<tm1Gldn>/Y,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	N	19439424
MGI:3844352	M	MP:0008770	decreased survivor rate	Arx<tm1Gldn>/Y,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	N	19439424
MGI:3844352	M	MP:0003631	nervous system phenotype	Arx<tm1Gldn>/Y,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	Y	19439424
MGI:3844352	M	MP:0000951	sporadic seizures	Arx<tm1Gldn>/Y,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	N	19439424
MGI:3844352	M	MP:0011086	postnatal lethality, incomplete penetrance	Arx<tm1Gldn>/Y,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	N	19439424
MGI:3844353	F	MP:0003997	tonic-clonic seizures	Arx<tm1Gldn>/Arx<+>,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	N	19439424
MGI:3844353	F	MP:0000951	sporadic seizures	Arx<tm1Gldn>/Arx<+>,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	N	19439424
MGI:3844353	F	MP:0003996	clonic seizures	Arx<tm1Gldn>/Arx<+>,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	N	19439424
MGI:3844353	F	MP:0003631	nervous system phenotype	Arx<tm1Gldn>/Arx<+>,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	Y	19439424
MGI:3844353	F	MP:0000947	convulsive seizures	Arx<tm1Gldn>/Arx<+>,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	N	19439424
MGI:3844353	F	MP:0004994	abnormal brain wave pattern	Arx<tm1Gldn>/Arx<+>,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	N	19439424
MGI:3844353	F	MP:0004101	abnormal brain interneuron morphology	Arx<tm1Gldn>/Arx<+>,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	N	19439424
MGI:3844430	F	MP:0006269	abnormal mammary gland growth during pregnancy	Ccnd1<tm1(CCNE)Pisc>/Ccnd1<tm1(CCNE)Pisc>	involves: 129/Sv * C57BL/6	N	10380928
MGI:3844431	F	MP:0006269	abnormal mammary gland growth during pregnancy	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas * C57BL/6	N	10380928
MGI:3844451	F	MP:0001923	reduced female fertility	Hoxa9<tm1Ipc>/Hoxa9<tm1Ipc>,Hoxd9<tm1Ipc>/Hoxd9<tm1Ipc>	involves: 129/Sv * 129S2/SvPas * C57BL/6	N	8625797
MGI:3844451	M	MP:0001922	reduced male fertility	Hoxa9<tm1Ipc>/Hoxa9<tm1Ipc>,Hoxd9<tm1Ipc>/Hoxd9<tm1Ipc>	involves: 129/Sv * 129S2/SvPas * C57BL/6	N	8625797
MGI:3844464	M	MP:0010768	mortality/aging	Ophn1<Wtgr>/Y	involves: C57BL/6J * DBA/2J	Y	MGI:3718087
MGI:3844465	M	MP:0010768	mortality/aging	Ophn1<Wtgr>/Y	involves: C57BL/6J * CAST/EiJ	Y	MGI:3718087
MGI:3844475	F	MP:0000628	abnormal mammary gland development	Hpse<tm1Jpli>/Hpse<tm1Jpli>	B6.129-Hpse<tm1Jpli>	N	19360105
MGI:3844518	M	MP:0001925	male infertility	Dync1h1<Swl>/Dync1h1<+>	involves: 101/H * C3H/HeH	N	MGI:60230
MGI:3844520	M	MP:0001360	abnormal social investigation	Tg(Thy1-Nlgn2)6Hnes/0	involves: C57BL/6 * CBA	N	18550748
MGI:3844571	F	MP:0010249	lactation failure	Elf5<tm1Sin>/Elf5<tm1Sin>,Tg(KRT14-cre)1Amc/0	involves: C57BL/6 * CBA	N	19269284
MGI:3844571	F	MP:0006269	abnormal mammary gland growth during pregnancy	Elf5<tm1Sin>/Elf5<tm1Sin>,Tg(KRT14-cre)1Amc/0	involves: C57BL/6 * CBA	N	19269284
MGI:3844572	F	MP:0001882	abnormal lactation	Elf5<tm1Sin>/Elf5<+>,Tg(KRT14-cre)1Amc/0	involves: C57BL/6 * CBA	N	19269284
MGI:3844572	F	MP:0006269	abnormal mammary gland growth during pregnancy	Elf5<tm1Sin>/Elf5<+>,Tg(KRT14-cre)1Amc/0	involves: C57BL/6 * CBA	N	19269284
MGI:3844573	F	MP:0001882	abnormal lactation	Elf5<tm1Sin>/Elf5<tm1Sin>,Tg(MMTV-cre)4Mam/0	involves: C57BL/6 * FVB	N	19269284
MGI:3844573	F	MP:0000628	abnormal mammary gland development	Elf5<tm1Sin>/Elf5<tm1Sin>,Tg(MMTV-cre)4Mam/0	involves: C57BL/6 * FVB	N	19269284
MGI:3844607	F	MP:0001923	reduced female fertility	Khdc3<tm1Dean>/Khdc3<tm1Dean>	involves: 129/Sv * C57BL/6	N	19376971
MGI:3844620	M	MP:0000858	abnormal metastatic potential	X/Tg(Wap-HRAS)69Lln	involves: C57BL/6 * SJL	N	2065330
MGI:3844620	M	MP:0000621	increased salivary adenocarcinoma incidence	X/Tg(Wap-HRAS)69Lln	involves: C57BL/6 * SJL	N	2065330
MGI:3844620	M	MP:0009308	increased adenocarcinoma incidence	X/Tg(Wap-HRAS)69Lln	involves: C57BL/6 * SJL	N	3469670
MGI:3844620	M	MP:0010299	increased mammary gland tumor incidence	X/Tg(Wap-HRAS)69Lln	involves: C57BL/6 * SJL	N	2065330
MGI:3844623	M	MP:0010299	increased mammary gland tumor incidence	X/Tg(Wap-HRAS)69Lln	FVB.Cg-Tg(Wap-HRAS)69Lln Chr Y<SJL>/J	N	15905717
MGI:3844814	F	MP:0008267	abnormal hippocampus CA3 region morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844814	F	MP:0009940	abnormal hippocampus pyramidal cell morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844814	F	MP:0002761	abnormal hippocampal mossy fiber morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844814	F	MP:0004101	abnormal brain interneuron morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844814	F	MP:0002945	abnormal inhibitory postsynaptic currents	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844814	F	MP:0002083	premature death	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844814	F	MP:0003997	tonic-clonic seizures	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844814	F	MP:0000812	abnormal dentate gyrus morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844814	F	MP:0000947	convulsive seizures	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844814	F	MP:0008262	abnormal hippocampus region morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844814	F	MP:0008285	abnormal hippocampus granule cell layer	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844814	F	MP:0008263	abnormal hippocampus CA1 region morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844814	F	MP:0011086	postnatal lethality, incomplete penetrance	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Dcx<tm1Caw>	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844816	M	MP:0008285	abnormal hippocampus granule cell layer	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844816	M	MP:0003997	tonic-clonic seizures	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844816	M	MP:0000947	convulsive seizures	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844816	M	MP:0002945	abnormal inhibitory postsynaptic currents	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844816	M	MP:0004101	abnormal brain interneuron morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844816	M	MP:0002083	premature death	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844816	M	MP:0009940	abnormal hippocampus pyramidal cell morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844816	M	MP:0011086	postnatal lethality, incomplete penetrance	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844816	M	MP:0000812	abnormal dentate gyrus morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844816	M	MP:0008262	abnormal hippocampus region morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844816	M	MP:0008263	abnormal hippocampus CA1 region morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844816	M	MP:0008267	abnormal hippocampus CA3 region morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844816	M	MP:0002761	abnormal hippocampal mossy fiber morphology	Dclk2<tm1.2Jgg>/Dclk2<tm1.2Jgg>,Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844817	M	MP:0008267	abnormal hippocampus CA3 region morphology	Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844817	M	MP:0002945	abnormal inhibitory postsynaptic currents	Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844817	M	MP:0002761	abnormal hippocampal mossy fiber morphology	Dcx<tm1Caw>/Y	involves: 129/Sv * C57BL/6	N	19342486
MGI:3844908	M	MP:0001925	male infertility	Large1<enr-Tg(MbpReg)36Pop>/Large1<enr-Tg(MbpReg)36Pop>	involves: C57BL/6J * DBA/2J	N	7506762
MGI:3844908	F	MP:0001923	reduced female fertility	Large1<enr-Tg(MbpReg)36Pop>/Large1<enr-Tg(MbpReg)36Pop>	involves: C57BL/6J * DBA/2J	N	7506762
MGI:3844909	M	MP:0013501	increased fibroblast apoptosis	Ikbkg<tm1Mpa>/Y	involves: C57BL/6	N	10911992
MGI:3844909	M	MP:0008561	decreased tumor necrosis factor secretion	Ikbkg<tm1Mpa>/Y	involves: C57BL/6	N	10911992
MGI:3844909	M	MP:0008706	decreased interleukin-6 secretion	Ikbkg<tm1Mpa>/Y	involves: C57BL/6	N	10911992
MGI:3844909	M	MP:0011091	prenatal lethality, complete penetrance	Ikbkg<tm1Mpa>/Y	involves: C57BL/6	N	10911992
MGI:3844910	F	MP:0001219	thick epidermis	Ikbkg<tm1Mpa>/Ikbkg<+>	involves: C57BL/6	N	10911992
MGI:3844910	F	MP:0004947	skin inflammation	Ikbkg<tm1Mpa>/Ikbkg<+>	involves: C57BL/6	N	10911992
MGI:3844910	F	MP:0009385	abnormal dermal pigmentation	Ikbkg<tm1Mpa>/Ikbkg<+>	involves: C57BL/6	N	10911992
MGI:3844910	F	MP:0009387	abnormal epidermal pigmentation	Ikbkg<tm1Mpa>/Ikbkg<+>	involves: C57BL/6	N	10911992
MGI:3844910	F	MP:0001192	scaly skin	Ikbkg<tm1Mpa>/Ikbkg<+>	involves: C57BL/6	N	10911992
MGI:3844910	F	MP:0011086	postnatal lethality, incomplete penetrance	Ikbkg<tm1Mpa>/Ikbkg<+>	involves: C57BL/6	N	10911992
MGI:3844910	F	MP:0000424	retarded hair growth	Ikbkg<tm1Mpa>/Ikbkg<+>	involves: C57BL/6	N	10911992
MGI:3844910	F	MP:0003427	parakeratosis	Ikbkg<tm1Mpa>/Ikbkg<+>	involves: C57BL/6	N	10911992
MGI:3844910	F	MP:0009580	increased keratinocyte apoptosis	Ikbkg<tm1Mpa>/Ikbkg<+>	involves: C57BL/6	N	10911992
MGI:3844910	F	MP:0001231	abnormal epidermis stratum basale morphology	Ikbkg<tm1Mpa>/Ikbkg<+>	involves: C57BL/6	N	10911992
MGI:3844910	F	MP:0001732	postnatal growth retardation	Ikbkg<tm1Mpa>/Ikbkg<+>	involves: C57BL/6	N	10911992
MGI:3844910	F	MP:0001233	abnormal epidermis suprabasal layer morphology	Ikbkg<tm1Mpa>/Ikbkg<+>	involves: C57BL/6	N	10911992
MGI:3844910	F	MP:0002655	abnormal keratinocyte morphology	Ikbkg<tm1Mpa>/Ikbkg<+>	involves: C57BL/6	N	10911992
MGI:3844980	M	MP:0003415	priapism	Tg(Tek-cre)1Ywa/0,Thbd<tm2Rdr>/Thbd<tm2Wlr>	involves: 129S2/SvPas * C57BL/6 * SJL	N	11518727
MGI:3844991	F	MP:0020519	renal glomerular immunoglobulin deposits	Sle1c<NZB>/Sle1c<NZM2410/J>	involves: C57BL/6J * NZB * NZM2410/J	N	17372026
MGI:3844991	F	MP:0002743	glomerulonephritis	Sle1c<NZB>/Sle1c<NZM2410/J>	involves: C57BL/6J * NZB * NZM2410/J	N	17372026
MGI:3844991	F	MP:0003725	increased autoantibody level	Sle1c<NZB>/Sle1c<NZM2410/J>	involves: C57BL/6J * NZB * NZM2410/J	N	17372026
MGI:3845008	M	MP:0002020	increased tumor incidence	Tg(Tcra,Tcrb)HRVAll/0,Tg(TRAMP)8247Ng/0	B6.Cg-Tg(TRAMP)8247Ng Tg(Tcra,Tcrb)HRVAll	N	18187659
MGI:3845008	M	MP:0002083	premature death	Tg(Tcra,Tcrb)HRVAll/0,Tg(TRAMP)8247Ng/0	B6.Cg-Tg(TRAMP)8247Ng Tg(Tcra,Tcrb)HRVAll	N	18187659
MGI:3845008	M	MP:0010357	increased prostate gland tumor incidence	Tg(Tcra,Tcrb)HRVAll/0,Tg(TRAMP)8247Ng/0	B6.Cg-Tg(TRAMP)8247Ng Tg(Tcra,Tcrb)HRVAll	N	18187659
MGI:3845037	M	MP:0010386	abnormal urinary bladder physiology	Kcnma1<tm1Ruth>/Kcnma1<tm2.1Ruth>,X/Tg(Myh11-icre/ERT2)1Soff	involves: 129/Sv * C57BL/6 * FVB/N	N	19220851
MGI:3845037	M	MP:0011535	increased urination frequency	Kcnma1<tm1Ruth>/Kcnma1<tm2.1Ruth>,X/Tg(Myh11-icre/ERT2)1Soff	involves: 129/Sv * C57BL/6 * FVB/N	N	19220851
MGI:3845037	M	MP:0005620	abnormal muscle contractility	Kcnma1<tm1Ruth>/Kcnma1<tm2.1Ruth>,X/Tg(Myh11-icre/ERT2)1Soff	involves: 129/Sv * C57BL/6 * FVB/N	N	19220851
MGI:3845794	M	MP:0001922	reduced male fertility	Tg(PMP22)C22Clh/0	involves: C57BL/6J * CBA/Ca	N	8733121
MGI:3845908	M	MP:0001922	reduced male fertility	Oprm1<tm1Lyu>/Oprm1<tm1Lyu>	involves: Black Swiss	N	9126934
MGI:3845908	M	MP:0002687	oligozoospermia	Oprm1<tm1Lyu>/Oprm1<tm1Lyu>	involves: Black Swiss	N	9126934
MGI:3845908	M	MP:0002675	asthenozoospermia	Oprm1<tm1Lyu>/Oprm1<tm1Lyu>	involves: Black Swiss	N	9126934
MGI:3845908	M	MP:0001380	reduced male mating frequency	Oprm1<tm1Lyu>/Oprm1<tm1Lyu>	involves: Black Swiss	N	9126934
MGI:3845909	M	MP:0001380	reduced male mating frequency	Oprm1<tm1Lyu>/Oprm1<+>	involves: Black Swiss	N	9126934
MGI:3845913	F	MP:0009503	abnormal mammary gland duct morphology	Bcl2l11<tm1.1Jad>/Bcl2l11<tm1.1Jad>	involves: C57BL/6	N	14635229
MGI:3845913	F	MP:0000628	abnormal mammary gland development	Bcl2l11<tm1.1Jad>/Bcl2l11<tm1.1Jad>	involves: C57BL/6	N	14635229
MGI:3845916	F	MP:0009327	abnormal maternal grooming	Grin1<tm1.1Phs>/Grin1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10729336
MGI:3845916	F	MP:0009326	absent maternal crouching	Grin1<tm1.1Phs>/Grin1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10729336
MGI:3845916	F	MP:0001384	abnormal pup retrieval	Grin1<tm1.1Phs>/Grin1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10729336
MGI:3845916	F	MP:0001386	abnormal maternal nurturing	Grin1<tm1.1Phs>/Grin1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10729336
MGI:3845916	F	MP:0001385	pup cannibalization	Grin1<tm1.1Phs>/Grin1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10729336
MGI:3845916	F	MP:0001399	hyperactivity	Grin1<tm1.1Phs>/Grin1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	10729336
MGI:3846064	F	MP:0001926	female infertility	Egr1<tm1The>/Egr1<tm1The>	involves: 129S7/SvEvBrd * C57BL/6	N	11739581
MGI:3846126	M	MP:0002673	abnormal sperm number	T(7;18)50H/+	involves: 101/H * C3H/HeH * CBA/H	N	2072976
MGI:3846126	M	MP:0001922	reduced male fertility	T(7;18)50H/+	involves: 101/H * C3H/HeH * CBA/H	N	2072976
MGI:3846126	M	MP:0002687	oligozoospermia	T(7;18)50H/+	involves: 101/H * C3H/HeH * CBA/H	N	2072976
MGI:3846126	M	MP:0004852	decreased testis weight	T(7;18)50H/+	involves: 101/H * C3H/HeH * CBA/H	N	2072976
MGI:3846126	F	MP:0001923	reduced female fertility	T(7;18)50H/+	involves: 101/H * C3H/HeH * CBA/H	N	2072976
MGI:3846126	M	MP:0009230	abnormal sperm head morphology	T(7;18)50H/+	involves: 101/H * C3H/HeH * CBA/H	N	2072976
MGI:3846128	F	MP:0001923	reduced female fertility	T(7;18)50H/+	involves: 101/H * C3H/HeH * C57BL/6J	N	2072976
MGI:3846128	M	MP:0009230	abnormal sperm head morphology	T(7;18)50H/+	involves: 101/H * C3H/HeH * C57BL/6J	N	2072976
MGI:3846128	M	MP:0001922	reduced male fertility	T(7;18)50H/+	involves: 101/H * C3H/HeH * C57BL/6J	N	2072976
MGI:3846128	M	MP:0002687	oligozoospermia	T(7;18)50H/+	involves: 101/H * C3H/HeH * C57BL/6J	N	2072976
MGI:3846128	M	MP:0004852	decreased testis weight	T(7;18)50H/+	involves: 101/H * C3H/HeH * C57BL/6J	N	2072976
MGI:3846354	M	MP:0001925	male infertility	Gli2<tm3.1(Gli1)Alj>/Gli2<+>,Gli3<Xt-J>/Gli3<+>	either: (involves: 129S6/SvEvTac * C3H/HeJ) or (involves: 129S6/SvEvTac * Black Swiss * C3H/HeJ)	N	11748151
MGI:3846425	M	MP:0011467	decreased urine urea nitrogen level	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	16985211
MGI:3846425	M	MP:0003311	aminoaciduria	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	16985211
MGI:3846425	M	MP:0010958	abnormal tricarboxylic acid cycle	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	19246514
MGI:3846425	M	MP:0001762	polyuria	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	16985211
MGI:3846425	M	MP:0002988	decreased urine osmolality	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	16985211
MGI:3846425	M	MP:0030644	increased circulating methionine level	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	16985211
MGI:3846425	M	MP:0002891	increased insulin sensitivity	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	19246514
MGI:3846425	M	MP:0006317	decreased urine sodium level	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	16985211
MGI:3846425	M	MP:0009643	abnormal urine homeostasis	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	19246514
MGI:3846425	M	MP:0013723	increased circulating tyrosine level	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	16985211
MGI:3846425	M	MP:0009645	crystalluria	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	16985211
MGI:3846425	M	MP:0001433	polyphagia	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	16985211
MGI:3846425	M	MP:0002575	increased circulating ketone body level	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	19246514
MGI:3846425	M	MP:0003978	decreased circulating carnitine level	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	19246514
MGI:3846425	M	MP:0001262	decreased body weight	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	19246514
MGI:3846425	M	MP:0005459	decreased percent body fat/body weight	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	19246514
MGI:3846425	M	MP:0002106	abnormal muscle physiology	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	19246514
MGI:3846425	M	MP:0005633	increased circulating sodium level	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	16985211
MGI:3846425	M	MP:0005332	abnormal amino acid level	Cltrn<tm1Thu>/Y	involves: 129S/SvEv * C57BL/6	N	19246514
MGI:3846696	M	MP:0004901	decreased male germ cell number	Kif18a<gcd2>/Kif18a<gcd2>	CAST.129S1(B6)-Kif18a<gcd2>/JcsJ	N	16822657
MGI:3846696	F	MP:0005431	decreased oocyte number	Kif18a<gcd2>/Kif18a<gcd2>	CAST.129S1(B6)-Kif18a<gcd2>/JcsJ	N	16822657
MGI:3846696	F	MP:0001926	female infertility	Kif18a<gcd2>/Kif18a<gcd2>	CAST.129S1(B6)-Kif18a<gcd2>/JcsJ	N	16822657
MGI:3846696	M	MP:0001925	male infertility	Kif18a<gcd2>/Kif18a<gcd2>	CAST.129S1(B6)-Kif18a<gcd2>/JcsJ	N	16822657
MGI:3846698	F	MP:0001926	female infertility	Kif18a<gcd2>/Kif18a<gcd2>	B6.129S1-Kif18a<gcd2>/JcsJ	N	16822657
MGI:3846698	M	MP:0001925	male infertility	Kif18a<gcd2>/Kif18a<gcd2>	B6.129S1-Kif18a<gcd2>/JcsJ	N	16822657
MGI:3846742	F	MP:0001828	abnormal T cell activation	Hprt1<tm1(CAG-Tgfbr1*)Lba>/Hprt1<tm1(CAG-Tgfbr1*)Lba>,Tg(Cd4-cre)1Cwi/0	involves: 129 * C57BL/6 * DBA/2	N	18821589
MGI:3846744	M	MP:0001828	abnormal T cell activation	Hprt1<tm1(CAG-Tgfbr1*)Lba>/Y,Tg(Cd4-cre)1Cwi/0	involves: 129 * C57BL/6 * DBA/2	N	18821589
MGI:3846745	M	MP:0005387	immune system phenotype	Hprt1<tm1(CAG-Tgfbr1*)Lba>/Y,Tgfbr2<tm1.2Hlm>/Tgfbr2<tm1.2Hlm>,Tg(Cd4-cre)1Cwi/0	involves: 129 * 129S6/SvEvTac * C57BL/6 * DBA/2	Y	18821589
MGI:3846748	F	MP:0005387	immune system phenotype	Hprt1<tm1(CAG-Tgfbr1*)Lba>/Hprt1<tm1(CAG-Tgfbr1*)Lba>,Tgfbr2<tm1.2Hlm>/Tgfbr2<tm1.2Hlm>,Tg(Cd4-cre)1Cwi/0	involves: 129 * 129S6/SvEvTac * C57BL/6 * DBA/2	Y	18821589
MGI:3846775	M	MP:0002687	oligozoospermia	T(7;18)50H/+	involves: 101/H * C3H/HeH * C57BL/6J	N	2072976
MGI:3846775	M	MP:0004852	decreased testis weight	T(7;18)50H/+	involves: 101/H * C3H/HeH * C57BL/6J	N	2072976
MGI:3846775	F	MP:0001923	reduced female fertility	T(7;18)50H/+	involves: 101/H * C3H/HeH * C57BL/6J	N	2072976
MGI:3846775	M	MP:0001922	reduced male fertility	T(7;18)50H/+	involves: 101/H * C3H/HeH * C57BL/6J	N	2072976
MGI:3846775	M	MP:0009230	abnormal sperm head morphology	T(7;18)50H/+	involves: 101/H * C3H/HeH * C57BL/6J	N	2072976
MGI:3847083	M	MP:0001925	male infertility	Golga3<Tg(06MGMT)T604Kccri>/Golga3<Tg(06MGMT)T604Kccri>	involves: C3H * C57BL/6	N	9892724
MGI:3847083	M	MP:0009230	abnormal sperm head morphology	Golga3<Tg(06MGMT)T604Kccri>/Golga3<Tg(06MGMT)T604Kccri>	involves: C3H * C57BL/6	N	9892724
MGI:3847083	M	MP:0002687	oligozoospermia	Golga3<Tg(06MGMT)T604Kccri>/Golga3<Tg(06MGMT)T604Kccri>	involves: C3H * C57BL/6	N	9892724
MGI:3847083	M	MP:0001147	small testis	Golga3<Tg(06MGMT)T604Kccri>/Golga3<Tg(06MGMT)T604Kccri>	involves: C3H * C57BL/6	N	9892724
MGI:3847224	F	MP:0000745	tremors	jpl/jpl	B6;D2-jpl	N	MGI:2180094
MGI:3847224	F	MP:0003633	abnormal nervous system physiology	jpl/jpl	B6;D2-jpl	N	MGI:2180094
MGI:3847224	F	MP:0002083	premature death	jpl/jpl	B6;D2-jpl	N	MGI:2180094
MGI:3847224	F	MP:0002066	abnormal motor capabilities/coordination/movement	jpl/jpl	B6;D2-jpl	N	MGI:2180094
MGI:3847269	M	MP:0001925	male infertility	Grid2<ho-Btlr>/Grid2<ho-Btlr>	C57BL/6J-Grid2<ho-Btlr>	N	MGI:3847246
MGI:3847710	M	MP:0014052	increased male germ cell apoptosis	Tdrd6<tm1Jess>/Tdrd6<tm1Jess>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	19345099
MGI:3847710	M	MP:0005159	azoospermia	Tdrd6<tm1Jess>/Tdrd6<tm1Jess>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	19345099
MGI:3847710	M	MP:0001155	arrest of spermatogenesis	Tdrd6<tm1Jess>/Tdrd6<tm1Jess>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	19345099
MGI:3847710	M	MP:0001925	male infertility	Tdrd6<tm1Jess>/Tdrd6<tm1Jess>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	19345099
MGI:3847710	M	MP:0001147	small testis	Tdrd6<tm1Jess>/Tdrd6<tm1Jess>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	N	19345099
MGI:3847919	F	MP:0004256	abnormal maternal decidual layer morphology	Elavl1<tm1.2Dkon>/Elavl1<tm1.2Dkon>	involves: 129P2/OlaHsd * C57BL/6	N	19307312
MGI:3847937	F	MP:0006269	abnormal mammary gland growth during pregnancy	Tg(MMTV-NFKBIA*S32A*S36A)13Mka/?	involves: C57BL/6	N	11747812
MGI:3847937	F	MP:0001882	abnormal lactation	Tg(MMTV-NFKBIA*S32A*S36A)13Mka/?	involves: C57BL/6	N	11747812
MGI:3848006	F	MP:0001926	female infertility	Elovl5<Gt(DTM098)Byg>/Elovl5<Gt(DTM098)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	18838740
MGI:3848030	F	MP:0002169	no abnormal phenotype detected	Gab3<tm1Lrr>/Gab3<tm1Lrr>	involves: 129S4/SvJae * C57BL/6	N	12640125
MGI:3848333	F	MP:0001923	reduced female fertility	Dppa4<tm1.1Hjf>/Dppa4<tm1.1Hjf>	B6.129P2-Dppa4<tm1.1Hjf>	N	19332562
MGI:3848358	M	MP:0004852	decreased testis weight	Prdx4<tm1.1Jufu>/Y	involves: C57BL/6	N	19105792
MGI:3848358	M	MP:0014052	increased male germ cell apoptosis	Prdx4<tm1.1Jufu>/Y	involves: C57BL/6	N	19105792
MGI:3848358	M	MP:0003674	oxidative stress	Prdx4<tm1.1Jufu>/Y	involves: C57BL/6	N	19105792
MGI:3848358	M	MP:0003205	testicular atrophy	Prdx4<tm1.1Jufu>/Y	involves: C57BL/6	N	19105792
MGI:3848358	M	MP:0002687	oligozoospermia	Prdx4<tm1.1Jufu>/Y	involves: C57BL/6	N	19105792
MGI:3848443	M	MP:0005389	reproductive system phenotype	Nxf2<tm1.2Jw>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	Y	19345203
MGI:3848443	M	MP:0008280	abnormal male germ cell apoptosis	Nxf2<tm1.2Jw>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	19345203
MGI:3848443	M	MP:0004852	decreased testis weight	Nxf2<tm1.2Jw>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	19345203
MGI:3848443	M	MP:0005169	abnormal male meiosis	Nxf2<tm1.2Jw>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	19345203
MGI:3848443	M	MP:0001925	male infertility	Nxf2<tm1.2Jw>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	19345203
MGI:3848443	M	MP:0004218	meiotic nondisjunction during M1 phase	Nxf2<tm1.2Jw>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	19345203
MGI:3848443	M	MP:0008261	arrest of male meiosis	Nxf2<tm1.2Jw>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	19345203
MGI:3848444	M	MP:0002685	abnormal spermatogonia proliferation	Nxf2<tm1.2Jw>/Y	B6.Cg-Nxf2<tm1.2Jw>	N	19345203
MGI:3848444	M	MP:0001925	male infertility	Nxf2<tm1.2Jw>/Y	B6.Cg-Nxf2<tm1.2Jw>	N	19345203
MGI:3848444	M	MP:0008995	early reproductive senescence	Nxf2<tm1.2Jw>/Y	B6.Cg-Nxf2<tm1.2Jw>	N	19345203
MGI:3848444	M	MP:0001153	small seminiferous tubules	Nxf2<tm1.2Jw>/Y	B6.Cg-Nxf2<tm1.2Jw>	N	19345203
MGI:3848444	M	MP:0005389	reproductive system phenotype	Nxf2<tm1.2Jw>/Y	B6.Cg-Nxf2<tm1.2Jw>	Y	19345203
MGI:3848444	M	MP:0002687	oligozoospermia	Nxf2<tm1.2Jw>/Y	B6.Cg-Nxf2<tm1.2Jw>	N	19345203
MGI:3848444	M	MP:0002675	asthenozoospermia	Nxf2<tm1.2Jw>/Y	B6.Cg-Nxf2<tm1.2Jw>	N	19345203
MGI:3848444	M	MP:0001156	abnormal spermatogenesis	Nxf2<tm1.2Jw>/Y	B6.Cg-Nxf2<tm1.2Jw>	N	19345203
MGI:3848444	M	MP:0001922	reduced male fertility	Nxf2<tm1.2Jw>/Y	B6.Cg-Nxf2<tm1.2Jw>	N	19345203
MGI:3848444	M	MP:0006378	abnormal spermatogonia morphology	Nxf2<tm1.2Jw>/Y	B6.Cg-Nxf2<tm1.2Jw>	N	19345203
MGI:3848444	M	MP:0004901	decreased male germ cell number	Nxf2<tm1.2Jw>/Y	B6.Cg-Nxf2<tm1.2Jw>	N	19345203
MGI:3848444	M	MP:0004852	decreased testis weight	Nxf2<tm1.2Jw>/Y	B6.Cg-Nxf2<tm1.2Jw>	N	19345203
MGI:3848444	M	MP:0001935	decreased litter size	Nxf2<tm1.2Jw>/Y	B6.Cg-Nxf2<tm1.2Jw>	N	19345203
MGI:3848461	F	MP:0009222	increased uterus tumor incidence	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	11940649
MGI:3848616	F	MP:0005560	decreased circulating glucose level	Gk<tm1Wjc>/Gk<+>	involves: 129S7/SvEvBrd	N	19270708
MGI:3848616	F	MP:0005282	decreased fatty acids level	Gk<tm1Wjc>/Gk<+>	involves: 129S7/SvEvBrd	N	19270708
MGI:3848704	M	MP:0001167	prostate gland epithelial hyperplasia	Serpinf1<tm1Craw>/Serpinf1<+>	involves: 129X1/SvJ * C57BL/6J	N	12740569
MGI:3848704	M	MP:0001158	abnormal prostate gland morphology	Serpinf1<tm1Craw>/Serpinf1<+>	involves: 129X1/SvJ * C57BL/6J	N	12740569
MGI:3848801	M	MP:0004810	decreased hematopoietic stem cell number	Zfx<tm1.1Reiz>/Y,Gt(ROSA)26Sor<tm1(cre/ERT2)Thl>/Gt(ROSA)26Sor<+>	involves: 129/Sv * 129S6/SvEvTac	N	17448993
MGI:3848801	M	MP:0001545	abnormal hematopoietic system physiology	Zfx<tm1.1Reiz>/Y,Gt(ROSA)26Sor<tm1(cre/ERT2)Thl>/Gt(ROSA)26Sor<+>	involves: 129/Sv * 129S6/SvEvTac	N	17448993
MGI:3848801	M	MP:0008249	abnormal common lymphocyte progenitor cell morphology	Zfx<tm1.1Reiz>/Y,Gt(ROSA)26Sor<tm1(cre/ERT2)Thl>/Gt(ROSA)26Sor<+>	involves: 129/Sv * 129S6/SvEvTac	N	17448993
MGI:3848802	M	MP:0011087	neonatal lethality, complete penetrance	Zfx<tm1.1Reiz>/Y,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	N	17448993
MGI:3848803	M	MP:0003631	nervous system phenotype	Zfx<tm1.1Reiz>/Y,Tg(Nes-cre)1Kln/0	involves: 129S6/SvEvTac * C57BL/6 * SJL	Y	17448993
MGI:3848803	M	MP:0010768	mortality/aging	Zfx<tm1.1Reiz>/Y,Tg(Nes-cre)1Kln/0	involves: 129S6/SvEvTac * C57BL/6 * SJL	Y	17448993
MGI:3848804	M	MP:0001545	abnormal hematopoietic system physiology	Zfx<tm1.1Reiz>/Y,Tg(Tek-cre)12Flv/0	involves: 129S6/SvEvTac * C3H * C57BL/6	N	17448993
MGI:3848804	M	MP:0005018	decreased T cell number	Zfx<tm1.1Reiz>/Y,Tg(Tek-cre)12Flv/0	involves: 129S6/SvEvTac * C3H * C57BL/6	N	17448993
MGI:3848804	M	MP:0008249	abnormal common lymphocyte progenitor cell morphology	Zfx<tm1.1Reiz>/Y,Tg(Tek-cre)12Flv/0	involves: 129S6/SvEvTac * C3H * C57BL/6	N	17448993
MGI:3848804	M	MP:0008211	decreased mature B cell number	Zfx<tm1.1Reiz>/Y,Tg(Tek-cre)12Flv/0	involves: 129S6/SvEvTac * C3H * C57BL/6	N	17448993
MGI:3848804	M	MP:0004810	decreased hematopoietic stem cell number	Zfx<tm1.1Reiz>/Y,Tg(Tek-cre)12Flv/0	involves: 129S6/SvEvTac * C3H * C57BL/6	N	17448993
MGI:3848805	M	MP:0001545	abnormal hematopoietic system physiology	Zfx<tm1.1Reiz>/Y,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	17448993
MGI:3848805	M	MP:0004810	decreased hematopoietic stem cell number	Zfx<tm1.1Reiz>/Y,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	17448993
MGI:3848805	M	MP:0008249	abnormal common lymphocyte progenitor cell morphology	Zfx<tm1.1Reiz>/Y,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	17448993
MGI:3848805	M	MP:0005016	decreased lymphocyte cell number	Zfx<tm1.1Reiz>/Y,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	17448993
MGI:3848805	M	MP:0001606	impaired hematopoiesis	Zfx<tm1.1Reiz>/Y,Tg(Mx1-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	17448993
MGI:3848806	M	MP:0004810	decreased hematopoietic stem cell number	Zfx<tm1.2Reiz>/Y	involves: 129S6/SvEvTac * C57BL/6 * DBA/2	N	17448993
MGI:3848806	M	MP:0002086	abnormal extraembryonic tissue morphology	Zfx<tm1.2Reiz>/Y	involves: 129S6/SvEvTac * C57BL/6 * DBA/2	N	17448993
MGI:3848806	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Zfx<tm1.2Reiz>/Y	involves: 129S6/SvEvTac * C57BL/6 * DBA/2	N	17448993
MGI:3848807	F	MP:0002086	abnormal extraembryonic tissue morphology	Zfx<tm1.2Reiz>/Zfx<tm1.2Reiz>	involves: 129S6/SvEvTac * C57BL/6 * DBA/2	N	17448993
MGI:3848807	F	MP:0004810	decreased hematopoietic stem cell number	Zfx<tm1.2Reiz>/Zfx<tm1.2Reiz>	involves: 129S6/SvEvTac * C57BL/6 * DBA/2	N	17448993
MGI:3848807	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Zfx<tm1.2Reiz>/Zfx<tm1.2Reiz>	involves: 129S6/SvEvTac * C57BL/6 * DBA/2	N	17448993
MGI:3848808	F	MP:0011087	neonatal lethality, complete penetrance	Zfx<tm1.1Reiz>/Zfx<tm1.1Reiz>,Meox2<tm1(cre)Sor>/Meox2<+>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	N	17448993
MGI:3848809	F	MP:0003631	nervous system phenotype	Zfx<tm1.1Reiz>/Zfx<tm1.1Reiz>,Tg(Nes-cre)1Kln/0	involves: 129S6/SvEvTac * C57BL/6 * SJL	Y	17448993
MGI:3848809	F	MP:0010768	mortality/aging	Zfx<tm1.1Reiz>/Zfx<tm1.1Reiz>,Tg(Nes-cre)1Kln/0	involves: 129S6/SvEvTac * C57BL/6 * SJL	Y	17448993
MGI:3849073	F	MP:0002026	increased leukemia incidence	Rbm15<tm1.1(MAL)Dgg>/Rbm15<tm1.1(MAL)Dgg>	B6.129-Rbm15<tm1.1(MAL)Dgg>	N	19287095
MGI:3849073	F	MP:0004809	increased hematopoietic stem cell number	Rbm15<tm1.1(MAL)Dgg>/Rbm15<tm1.1(MAL)Dgg>	B6.129-Rbm15<tm1.1(MAL)Dgg>	N	19287095
MGI:3849073	F	MP:0000240	extramedullary hematopoiesis	Rbm15<tm1.1(MAL)Dgg>/Rbm15<tm1.1(MAL)Dgg>	B6.129-Rbm15<tm1.1(MAL)Dgg>	N	19287095
MGI:3849073	F	MP:0006410	abnormal common myeloid progenitor cell morphology	Rbm15<tm1.1(MAL)Dgg>/Rbm15<tm1.1(MAL)Dgg>	B6.129-Rbm15<tm1.1(MAL)Dgg>	N	19287095
MGI:3849294	M	MP:0001925	male infertility	Mpz<ttrr>/Mpz<ttrr>	B6.Cg-Mpz<ttrr>/GrsrJ	N	MGI:3849292
MGI:3849294	F	MP:0001926	female infertility	Mpz<ttrr>/Mpz<ttrr>	B6.Cg-Mpz<ttrr>/GrsrJ	N	MGI:3849292
MGI:3849325	F	MP:0005121	decreased circulating prolactin level	Trpc5<tm1.1Clph>/Trpc5<tm1.1Clph>	involves: 129S1/SvImJ	N	31285329
MGI:3849325	F	MP:0001923	reduced female fertility	Trpc5<tm1.1Clph>/Trpc5<tm1.1Clph>	involves: 129S1/SvImJ	N	31285329
MGI:3849325	F	MP:0003460	decreased fear-related response	Trpc5<tm1.1Clph>/Trpc5<tm1.1Clph>	involves: 129S1/SvImJ	N	19450521
MGI:3849325	F	MP:0005402	abnormal action potential	Trpc5<tm1.1Clph>/Trpc5<tm1.1Clph>	involves: 129S1/SvImJ	N	31285329
MGI:3849325	F	MP:0003459	increased fear-related response	Trpc5<tm1.1Clph>/Trpc5<tm1.1Clph>	involves: 129S1/SvImJ	N	19450521
MGI:3849325	F	MP:0002910	abnormal excitatory postsynaptic currents	Trpc5<tm1.1Clph>/Trpc5<tm1.1Clph>	involves: 129S1/SvImJ	N	19450521
MGI:3849325	F	MP:0001364	decreased anxiety-related response	Trpc5<tm1.1Clph>/Trpc5<tm1.1Clph>	involves: 129S1/SvImJ	N	19450521
MGI:3849325	F	MP:0001935	decreased litter size	Trpc5<tm1.1Clph>/Trpc5<tm1.1Clph>	involves: 129S1/SvImJ	N	31285329
MGI:3849325	F	MP:0009006	prolonged estrous cycle	Trpc5<tm1.1Clph>/Trpc5<tm1.1Clph>	involves: 129S1/SvImJ	N	31285329
MGI:3849326	M	MP:0003459	increased fear-related response	Trpc5<tm1.1Clph>/Y	involves: 129S1/SvImJ	N	19450521
MGI:3849326	M	MP:0003460	decreased fear-related response	Trpc5<tm1.1Clph>/Y	involves: 129S1/SvImJ	N	19450521
MGI:3849326	M	MP:0001364	decreased anxiety-related response	Trpc5<tm1.1Clph>/Y	involves: 129S1/SvImJ	N	19450521
MGI:3849326	M	MP:0002910	abnormal excitatory postsynaptic currents	Trpc5<tm1.1Clph>/Y	involves: 129S1/SvImJ	N	19450521
MGI:3849568	F	MP:0001923	reduced female fertility	Foxa2<tm1Dnl>/Foxa2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	8069910
MGI:3849568	F	MP:0031434	increased miscarriage rate	Foxa2<tm1Dnl>/Foxa2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	8069910
MGI:3849568	F	MP:0009021	absent estrus	Foxa2<tm1Dnl>/Foxa2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	8069910
MGI:3849568	F	MP:0009009	absent estrous cycle	Foxa2<tm1Dnl>/Foxa2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	8069910
MGI:3849570	F	MP:0008092	abnormal T-helper 2 cell differentiation	Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129S/SvEv * C57BL/6	N	22692895
MGI:3849570	F	MP:0008700	decreased interleukin-4 secretion	Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129S/SvEv * C57BL/6	N	22692895
MGI:3849570	F	MP:0005014	increased B cell number	Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129S/SvEv * C57BL/6	N	22692895
MGI:3849570	F	MP:0003408	increased width of hypertrophic chondrocyte zone	Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129S/SvEv * C57BL/6	N	22692895
MGI:3849570	F	MP:0008699	increased interleukin-4 secretion	Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129S/SvEv * C57BL/6	N	22692895
MGI:3849570	F	MP:0010124	decreased bone mineral content	Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129S/SvEv * C57BL/6	N	22692895
MGI:3849570	F	MP:0008688	decreased interleukin-2 secretion	Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129S/SvEv * C57BL/6	N	22692895
MGI:3849570	F	MP:0008682	decreased interleukin-17 secretion	Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129S/SvEv * C57BL/6	N	22692895
MGI:3849570	F	MP:0008661	decreased interleukin-10 secretion	Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129S/SvEv * C57BL/6	N	22692895
MGI:3849570	F	MP:0008127	decreased dendritic cell number	Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129S/SvEv * C57BL/6	N	22692895
MGI:3849570	F	MP:0013763	increased T-helper cell number	Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129S/SvEv * C57BL/6	N	22692895
MGI:3849570	F	MP:0020010	decreased bone mineral density of femur	Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129S/SvEv * C57BL/6	N	22692895
MGI:3849570	F	MP:0000559	abnormal femur morphology	Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129S/SvEv * C57BL/6	N	22692895
MGI:3849590	M	MP:0008396	abnormal osteoclast differentiation	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	15936336
MGI:3849590	M	MP:0010551	abnormal coronary vessel morphology	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	19733558
MGI:3849590	M	MP:0010419	inlet ventricular septal defect	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	19733558
MGI:3849590	M	MP:0010418	perimembraneous ventricular septal defect	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	19733558
MGI:3849590	M	MP:0010413	complete atrioventricular septal defect	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	19733558
MGI:3849590	M	MP:0010402	ventricular septal defect	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	19733558
MGI:3849590	M	MP:0003384	abnormal ventral body wall morphology	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	10964473
MGI:3849590	M	MP:0003675	kidney cyst	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	10964473
MGI:3849590	M	MP:0008272	abnormal endochondral bone ossification	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	15936336
MGI:3849590	M	MP:0010146	umbilical hernia	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	10964473
MGI:3849590	M	MP:0003014	abnormal kidney medulla morphology	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	10964473
MGI:3849590	M	MP:0003139	patent ductus arteriosus	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	19733558
MGI:3849590	M	MP:0000284	double outlet right ventricle	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	19733558
MGI:3849590	M	MP:0001264	increased body size	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	10964473
MGI:3849590	M	MP:0010607	common atrioventricular valve	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	19733558
MGI:3849590	M	MP:0010476	coronary fistula	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	19733558
MGI:3849590	M	MP:0011090	perinatal lethality, incomplete penetrance	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	10964473
MGI:3849590	M	MP:0004678	split xiphoid process	Gpc3<tm1Snd>/Y	involves: 129X1/SvJ * C57BL/6	N	10964473
MGI:3849591	F	MP:0004678	split xiphoid process	Gpc3<tm1Snd>/Gpc3<+>	involves: 129X1/SvJ * C57BL/6	N	10964473
MGI:3849591	F	MP:0003384	abnormal ventral body wall morphology	Gpc3<tm1Snd>/Gpc3<+>	involves: 129X1/SvJ * C57BL/6	N	10964473
MGI:3849591	F	MP:0003675	kidney cyst	Gpc3<tm1Snd>/Gpc3<+>	involves: 129X1/SvJ * C57BL/6	N	10964473
MGI:3849591	F	MP:0001264	increased body size	Gpc3<tm1Snd>/Gpc3<+>	involves: 129X1/SvJ * C57BL/6	N	10964473
MGI:3849591	F	MP:0003014	abnormal kidney medulla morphology	Gpc3<tm1Snd>/Gpc3<+>	involves: 129X1/SvJ * C57BL/6	N	10964473
MGI:3849592	M	MP:0011307	kidney medulla cyst	Gpc3<Gt(Ex136)Byg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10964473
MGI:3849592	M	MP:0011090	perinatal lethality, incomplete penetrance	Gpc3<Gt(Ex136)Byg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10964473
MGI:3849592	M	MP:0003384	abnormal ventral body wall morphology	Gpc3<Gt(Ex136)Byg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10964473
MGI:3849592	M	MP:0001264	increased body size	Gpc3<Gt(Ex136)Byg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10964473
MGI:3849592	M	MP:0003014	abnormal kidney medulla morphology	Gpc3<Gt(Ex136)Byg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10964473
MGI:3849592	M	MP:0004678	split xiphoid process	Gpc3<Gt(Ex136)Byg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10964473
MGI:3849593	F	MP:0001264	increased body size	Gpc3<Gt(Ex136)Byg>/Gpc3<+>	involves: 129P2/OlaHsd * C57BL/6	N	10964473
MGI:3849593	F	MP:0003384	abnormal ventral body wall morphology	Gpc3<Gt(Ex136)Byg>/Gpc3<+>	involves: 129P2/OlaHsd * C57BL/6	N	10964473
MGI:3849593	F	MP:0011307	kidney medulla cyst	Gpc3<Gt(Ex136)Byg>/Gpc3<+>	involves: 129P2/OlaHsd * C57BL/6	N	10964473
MGI:3849593	F	MP:0004678	split xiphoid process	Gpc3<Gt(Ex136)Byg>/Gpc3<+>	involves: 129P2/OlaHsd * C57BL/6	N	10964473
MGI:3849593	F	MP:0003014	abnormal kidney medulla morphology	Gpc3<Gt(Ex136)Byg>/Gpc3<+>	involves: 129P2/OlaHsd * C57BL/6	N	10964473
MGI:3849594	M	MP:0000562	polydactyly	Bmp4<tm1Blh>/Bmp4<+>,Gpc3<Gt(Ex136)Byg>/Y	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	N	10964473
MGI:3849594	M	MP:0000154	rib fusion	Bmp4<tm1Blh>/Bmp4<+>,Gpc3<Gt(Ex136)Byg>/Y	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	N	10964473
MGI:3849594	M	MP:0008277	abnormal sternum ossification	Bmp4<tm1Blh>/Bmp4<+>,Gpc3<Gt(Ex136)Byg>/Y	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	N	10964473
MGI:3849594	M	MP:0000150	abnormal rib morphology	Bmp4<tm1Blh>/Bmp4<+>,Gpc3<Gt(Ex136)Byg>/Y	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	N	10964473
MGI:3849595	M	MP:0000150	abnormal rib morphology	Bmp4<tm1Blh>/Bmp4<+>,Gpc3<tm1Snd>/Y	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	10964473
MGI:3849595	M	MP:0008277	abnormal sternum ossification	Bmp4<tm1Blh>/Bmp4<+>,Gpc3<tm1Snd>/Y	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	10964473
MGI:3849595	M	MP:0000154	rib fusion	Bmp4<tm1Blh>/Bmp4<+>,Gpc3<tm1Snd>/Y	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	10964473
MGI:3849595	M	MP:0000562	polydactyly	Bmp4<tm1Blh>/Bmp4<+>,Gpc3<tm1Snd>/Y	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	N	10964473
MGI:3849600	M	MP:0002169	no abnormal phenotype detected	Dkc1<tm3Pjma>/Y	involves: 129X1/SvJ * C57BL/6J	N	19391112
MGI:3849601	F	MP:0002169	no abnormal phenotype detected	Dkc1<tm3Pjma>/Dkc1<tm3Pjma>	involves: 129X1/SvJ * C57BL/6J	N	19391112
MGI:3849602	M	MP:0002161	abnormal fertility/fecundity	Dkc1<tm2Pjma>/Y	chimera involves: 129X1/SvJ * C57BL/6J	N	19391112
MGI:3849602	M	MP:0005621	abnormal cell physiology	Dkc1<tm2Pjma>/Y	chimera involves: 129X1/SvJ * C57BL/6J	N	19391112
MGI:3849846	F	MP:0001385	pup cannibalization	Tph2<tm1Bdr>/Tph2<tm1Bdr>	involves: 129P2/OlaHsd * FVB/N	N	19520831
MGI:3849846	F	MP:0001386	abnormal maternal nurturing	Tph2<tm1Bdr>/Tph2<tm1Bdr>	involves: 129P2/OlaHsd * FVB/N	N	19520831
MGI:3849846	F	MP:0001384	abnormal pup retrieval	Tph2<tm1Bdr>/Tph2<tm1Bdr>	involves: 129P2/OlaHsd * FVB/N	N	19520831
MGI:3849892	M	MP:0001922	reduced male fertility	Lipe<tm1Gam>/Lipe<+>	involves: 129S4/SvJae	N	11564684
MGI:3850111	M	MP:0011626	orotic acid urinary bladder stones	Otc<spf>/Y	Not Specified	N	MGI:77872
MGI:3850111	M	MP:0001399	hyperactivity	Otc<spf>/Y	Not Specified	N	MGI:77872
MGI:3850111	M	MP:0008143	abnormal dendrite morphology	Otc<spf>/Y	Not Specified	N	9630607
MGI:3850111	M	MP:0005309	increased circulating ammonia level	Otc<spf>/Y	Not Specified	N	7707692
MGI:3850111	M	MP:0011588	decreased ornithine carbamoyltransferase activity	Otc<spf>/Y	Not Specified	N	7828023
MGI:3850111	M	MP:0003806	abnormal nucleotide metabolism	Otc<spf>/Y	Not Specified	N	1627360
MGI:3850111	M	MP:0009969	abnormal cerebral cortex pyramidal cell morphology	Otc<spf>/Y	Not Specified	N	9630607
MGI:3850111	M	MP:0030648	decreased ornithine level	Otc<spf>/Y	Not Specified	N	7828023
MGI:3850111	M	MP:0001265	decreased body size	Otc<spf>/Y	Not Specified	N	7707692
MGI:3850111	M	MP:0000416	sparse hair	Otc<spf>/Y	Not Specified	N	7707692
MGI:3850111	M	MP:0000774	decreased brain size	Otc<spf>/Y	Not Specified	N	9630607
MGI:3850111	M	MP:0011765	oroticaciduria	Otc<spf>/Y	Not Specified	N	7707692
MGI:3850111	M	MP:0000598	abnormal liver morphology	Otc<spf>/Y	Not Specified	N	7707692
MGI:3850111	M	MP:0011588	decreased ornithine carbamoyltransferase activity	Otc<spf>/Y	Not Specified	N	7707692
MGI:3850111	M	MP:0005311	abnormal circulating amino acid level	Otc<spf>/Y	Not Specified	N	7828023
MGI:3850111	M	MP:0005311	abnormal circulating amino acid level	Otc<spf>/Y	Not Specified	N	7707692
MGI:3850111	M	MP:0005332	abnormal amino acid level	Otc<spf>/Y	Not Specified	N	7828023
MGI:3850111	M	MP:0001399	hyperactivity	Otc<spf>/Y	Not Specified	N	7707692
MGI:3850111	M	MP:0002152	abnormal brain morphology	Otc<spf>/Y	Not Specified	N	7707692
MGI:3850111	M	MP:0011396	abnormal sleep behavior	Otc<spf>/Y	Not Specified	N	MGI:77872
MGI:3850111	M	MP:0000414	alopecia	Otc<spf>/Y	Not Specified	N	MGI:77872
MGI:3850111	M	MP:0011380	enlarged brain ventricles	Otc<spf>/Y	Not Specified	N	9630607
MGI:3850127	M	MP:0005390	skeleton phenotype	Efnb1<tm2.2Sor>/Y	involves: 129S4/SvJaeSor	Y	19515977
MGI:3850127	M	MP:0003631	nervous system phenotype	Efnb1<tm2.2Sor>/Y	involves: 129S4/SvJaeSor	Y	19515977
MGI:3850128	F	MP:0005390	skeleton phenotype	Efnb1<tm2.2Sor>/Efnb1<+>	involves: 129S4/SvJaeSor	Y	19515977
MGI:3850129	F	MP:0005390	skeleton phenotype	Efnb1<tm2.2Sor>/Efnb1<tm2.2Sor>	involves: 129S4/SvJaeSor	Y	19515977
MGI:3850129	F	MP:0003631	nervous system phenotype	Efnb1<tm2.2Sor>/Efnb1<tm2.2Sor>	involves: 129S4/SvJaeSor	Y	19515977
MGI:3850134	M	MP:0005390	skeleton phenotype	Efnb1<tm3.2Sor>/Y	involves: 129S4/SvJaeSor	Y	19515977
MGI:3850134	M	MP:0000780	abnormal corpus callosum morphology	Efnb1<tm3.2Sor>/Y	involves: 129S4/SvJaeSor	N	19515977
MGI:3850134	M	MP:0002196	absent corpus callosum	Efnb1<tm3.2Sor>/Y	involves: 129S4/SvJaeSor	N	19515977
MGI:3850135	F	MP:0005390	skeleton phenotype	Efnb1<tm3.2Sor>/Efnb1<+>	involves: 129S4/SvJaeSor	Y	19515977
MGI:3850135	F	MP:0002196	absent corpus callosum	Efnb1<tm3.2Sor>/Efnb1<+>	involves: 129S4/SvJaeSor	N	19515977
MGI:3850136	F	MP:0000780	abnormal corpus callosum morphology	Efnb1<tm3.2Sor>/Efnb1<tm3.2Sor>	involves: 129S4/SvJaeSor	N	19515977
MGI:3850136	F	MP:0005390	skeleton phenotype	Efnb1<tm3.2Sor>/Efnb1<tm3.2Sor>	involves: 129S4/SvJaeSor	Y	19515977
MGI:3850136	F	MP:0002196	absent corpus callosum	Efnb1<tm3.2Sor>/Efnb1<tm3.2Sor>	involves: 129S4/SvJaeSor	N	19515977
MGI:3850137	F	MP:0003631	nervous system phenotype	Efnb1<tm3.2Sor>/Efnb1<tm3.2Sor>	involves: 129S4/SvJaeSor * C57BL/6J * CBA/J	Y	19515977
MGI:3850138	M	MP:0003631	nervous system phenotype	Efnb1<tm3.2Sor>/Y	involves: 129S4/SvJaeSor * C57BL/6J * CBA/J	Y	19515977
MGI:3850139	F	MP:0003631	nervous system phenotype	Efnb1<tm3.2Sor>/Efnb1<+>	involves: 129S4/SvJaeSor * C57BL/6	Y	19515977
MGI:3850142	M	MP:0002196	absent corpus callosum	Efnb1<tm4.2Sor>/Y	involves: 129S4/SvJaeSor	N	19515977
MGI:3850142	M	MP:0003631	nervous system phenotype	Efnb1<tm4.2Sor>/Y	involves: 129S4/SvJaeSor	Y	19515977
MGI:3850142	M	MP:0005390	skeleton phenotype	Efnb1<tm4.2Sor>/Y	involves: 129S4/SvJaeSor	Y	19515977
MGI:3850143	F	MP:0003631	nervous system phenotype	Efnb1<tm4.2Sor>/Efnb1<tm4.2Sor>	involves: 129S4/SvJaeSor	Y	19515977
MGI:3850143	F	MP:0002196	absent corpus callosum	Efnb1<tm4.2Sor>/Efnb1<tm4.2Sor>	involves: 129S4/SvJaeSor	N	19515977
MGI:3850143	F	MP:0005390	skeleton phenotype	Efnb1<tm4.2Sor>/Efnb1<tm4.2Sor>	involves: 129S4/SvJaeSor	Y	19515977
MGI:3850144	M	MP:0005404	abnormal axon morphology	Efnb1<tm1.1Sor>/Y	involves: 129S4/SvJaeSor	N	21847105
MGI:3850144	M	MP:0002196	absent corpus callosum	Efnb1<tm1.1Sor>/Y	involves: 129S4/SvJaeSor	N	19515977
MGI:3850144	M	MP:0009890	cleft secondary palate	Efnb1<tm1.1Sor>/Y	involves: 129S4/SvJaeSor	N	19515977
MGI:3850144	M	MP:0000030	abnormal tympanic ring morphology	Efnb1<tm1.1Sor>/Y	involves: 129S4/SvJaeSor	N	19515977
MGI:3850144	M	MP:0000780	abnormal corpus callosum morphology	Efnb1<tm1.1Sor>/Y	involves: 129S4/SvJaeSor	N	19515977
MGI:3850144	M	MP:0000150	abnormal rib morphology	Efnb1<tm1.1Sor>/Y	involves: 129S4/SvJaeSor	N	19515977
MGI:3850145	F	MP:0002196	absent corpus callosum	Efnb1<tm4.2Sor>/Efnb1<+>	involves: 129S4/SvJaeSor	N	19515977
MGI:3850145	F	MP:0005390	skeleton phenotype	Efnb1<tm4.2Sor>/Efnb1<+>	involves: 129S4/SvJaeSor	Y	19515977
MGI:3850173	M	MP:0002152	abnormal brain morphology	Otc<spf>/Y	involves: C57BL/6	N	1531355
MGI:3850173	M	MP:0000436	abnormal head movements	Otc<spf>/Y	involves: C57BL/6	N	1531355
MGI:3850173	M	MP:0001777	abnormal body temperature homeostasis	Otc<spf>/Y	involves: C57BL/6	N	1531355
MGI:3850174	M	MP:0002082	postnatal lethality	Otc<spf>/Y	involves: 22A/R * C57BL/6J	N	5727
MGI:3850174	M	MP:0011626	orotic acid urinary bladder stones	Otc<spf>/Y	involves: 22A/R * C57BL/6J	N	5727
MGI:3850174	M	MP:0001265	decreased body size	Otc<spf>/Y	involves: 22A/R * C57BL/6J	N	5727
MGI:3850174	M	MP:0001211	wrinkled skin	Otc<spf>/Y	involves: 22A/R * C57BL/6J	N	5727
MGI:3850174	M	MP:0011588	decreased ornithine carbamoyltransferase activity	Otc<spf>/Y	involves: 22A/R * C57BL/6J	N	5727
MGI:3850174	M	MP:0000416	sparse hair	Otc<spf>/Y	involves: 22A/R * C57BL/6J	N	5727
MGI:3850182	M	MP:0005309	increased circulating ammonia level	Otc<spf>/Y	involves: CD-1	N	7816342
MGI:3850182	M	MP:0030706	increased glutamine level	Otc<spf>/Y	involves: CD-1	N	1575747
MGI:3850182	M	MP:0002152	abnormal brain morphology	Otc<spf>/Y	involves: CD-1	N	7816342
MGI:3850182	M	MP:0002152	abnormal brain morphology	Otc<spf>/Y	involves: CD-1	N	8041507
MGI:3850182	M	MP:0000598	abnormal liver morphology	Otc<spf>/Y	involves: CD-1	N	8108192
MGI:3850182	M	MP:0030709	increased circulating glutamine level	Otc<spf>/Y	involves: CD-1	N	1575747
MGI:3850182	M	MP:0002152	abnormal brain morphology	Otc<spf>/Y	involves: CD-1	N	8108192
MGI:3850182	M	MP:0001146	abnormal testis morphology	Otc<spf>/Y	involves: CD-1	N	8108192
MGI:3850182	M	MP:0005266	abnormal metabolism	Otc<spf>/Y	involves: CD-1	N	8424807
MGI:3850182	M	MP:0005584	abnormal enzyme/coenzyme activity	Otc<spf>/Y	involves: CD-1	N	8041507
MGI:3850182	M	MP:0005584	abnormal enzyme/coenzyme activity	Otc<spf>/Y	involves: CD-1	N	8424807
MGI:3850182	M	MP:0011765	oroticaciduria	Otc<spf>/Y	involves: CD-1	N	8221965
MGI:3850182	M	MP:0005584	abnormal enzyme/coenzyme activity	Otc<spf>/Y	involves: CD-1	N	7816342
MGI:3850182	M	MP:0005266	abnormal metabolism	Otc<spf>/Y	involves: CD-1	N	1575747
MGI:3850182	M	MP:0005309	increased circulating ammonia level	Otc<spf>/Y	involves: CD-1	N	1575747
MGI:3850182	M	MP:0001038	abnormal cholinergic neuron morphology	Otc<spf>/Y	involves: CD-1	N	7816342
MGI:3850182	M	MP:0011588	decreased ornithine carbamoyltransferase activity	Otc<spf>/Y	involves: CD-1	N	7816342
MGI:3850182	M	MP:0002135	abnormal kidney morphology	Otc<spf>/Y	involves: CD-1	N	8108192
MGI:3850182	M	MP:0005309	increased circulating ammonia level	Otc<spf>/Y	involves: CD-1	N	8424807
MGI:3850182	M	MP:0004000	impaired passive avoidance behavior	Otc<spf>/Y	involves: CD-1	N	8750014
MGI:3850212	F	MP:0001125	abnormal oocyte morphology	Dicer1<tm1.1Mnn>/Dicer1<tm1.2Mnn>,Tg(Zp3-cre)93Knw/0	involves: 129S1/SvImJ * C57BL/6J	N	19129368
MGI:3850212	F	MP:0005168	abnormal female meiosis	Dicer1<tm1.1Mnn>/Dicer1<tm1.2Mnn>,Tg(Zp3-cre)93Knw/0	involves: 129S1/SvImJ * C57BL/6J	N	19129368
MGI:3850212	F	MP:0001926	female infertility	Dicer1<tm1.1Mnn>/Dicer1<tm1.2Mnn>,Tg(Zp3-cre)93Knw/0	involves: 129S1/SvImJ * C57BL/6J	N	19129368
MGI:3850213	F	MP:0001125	abnormal oocyte morphology	Alpl<tm1(cre)Nagy>/Alpl<+>,Dicer1<tm1.1Mnn>/Dicer1<tm1.2Mnn>	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	19129368
MGI:3850221	F	MP:0013401	increased endometrial gland number	Errfi1<tm1Jwj>/Errfi1<tm1Jwj>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	19439667
MGI:3850221	F	MP:0001120	abnormal uterus morphology	Errfi1<tm1Jwj>/Errfi1<tm1Jwj>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	19439667
MGI:3850221	F	MP:0004904	increased uterus weight	Errfi1<tm1Jwj>/Errfi1<tm1Jwj>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	19439667
MGI:3850221	F	MP:0009092	endometrium hyperplasia	Errfi1<tm1Jwj>/Errfi1<tm1Jwj>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	19439667
MGI:3850221	F	MP:0001926	female infertility	Errfi1<tm1Jwj>/Errfi1<tm1Jwj>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	19439667
MGI:3850221	F	MP:0004868	increased endometrial carcinoma incidence	Errfi1<tm1Jwj>/Errfi1<tm1Jwj>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	19439667
MGI:3850440	F	MP:0003570	increased uterus leiomyoma incidence	Cdkn2a<tm2Brn>/Cdkn2a<tm2Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>	involves: 129P2/OlaHsd	N	18328429
MGI:3850443	F	MP:0003570	increased uterus leiomyoma incidence	Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18328429
MGI:3850444	F	MP:0003570	increased uterus leiomyoma incidence	Cdkn2a<tm2Brn>/Cdkn2a<tm2Brn>,Nf2<tm2Gth>/Nf2<+>	involves: 129P2/OlaHsd	N	18328429
MGI:3850445	F	MP:0003570	increased uterus leiomyoma incidence	Cdkn2a<tm2Brn>/Cdkn2a<+>,Nf2<tm2Gth>/Nf2<tm2Gth>	involves: 129P2/OlaHsd	N	18328429
MGI:3850446	F	MP:0003570	increased uterus leiomyoma incidence	Nf2<tm2Gth>/Nf2<+>,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18328429
MGI:3850447	F	MP:0003570	increased uterus leiomyoma incidence	Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<+>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18328429
MGI:3850512	M	MP:0010028	aciduria	Acads<del-J>/Acads<del-J>,Otc<spf>/Y	involves: BALB/cByJ * CD-1	N	8461026
MGI:3850512	M	MP:0002083	premature death	Acads<del-J>/Acads<del-J>,Otc<spf>/Y	involves: BALB/cByJ * CD-1	N	8461026
MGI:3850512	M	MP:0000416	sparse hair	Acads<del-J>/Acads<del-J>,Otc<spf>/Y	involves: BALB/cByJ * CD-1	N	8461026
MGI:3850513	F	MP:0010028	aciduria	Acads<del-J>/Acads<del-J>,Otc<spf>/Otc<+>	involves: BALB/cByJ * CD-1	N	8461026
MGI:3850518	M	MP:0010028	aciduria	Acads<del-J>/Acads<+>,Otc<spf>/Y	involves: BALB/cByJ * CD-1	N	8461026
MGI:3850518	M	MP:0011765	oroticaciduria	Acads<del-J>/Acads<+>,Otc<spf>/Y	involves: BALB/cByJ * CD-1	N	8461026
MGI:3850519	F	MP:0002083	premature death	Acads<del-J>/Acads<del-J>,Otc<spf>/Otc<spf>	involves: BALB/cByJ * CD-1	N	8461026
MGI:3850519	F	MP:0011765	oroticaciduria	Acads<del-J>/Acads<del-J>,Otc<spf>/Otc<spf>	involves: BALB/cByJ * CD-1	N	8461026
MGI:3850653	F	MP:0002073	abnormal hair growth	Otc<spf-ash>/Otc<spf>	Not Specified	N	4603259
MGI:3850818	F	MP:0020316	decreased vascular endothelial cell proliferation	Hprt1<tm1(Rcan1)Zyga>/Hprt1<+>	B6.129P2-Hprt1<tm1(Rcan1)Zyga>	N	19458618
MGI:3850818	F	MP:0003447	decreased tumor growth/size	Hprt1<tm1(Rcan1)Zyga>/Hprt1<+>	B6.129P2-Hprt1<tm1(Rcan1)Zyga>	N	19458618
MGI:3850853	M	MP:0006362	abnormal male germ cell morphology	Clcn2<tm1Mlv>/Clcn2<tm1Mlv>	involves: C57BL/6	N	11976342
MGI:3850853	M	MP:0001146	abnormal testis morphology	Clcn2<tm1Mlv>/Clcn2<tm1Mlv>	involves: C57BL/6	N	11976342
MGI:3850853	M	MP:0002784	abnormal Sertoli cell morphology	Clcn2<tm1Mlv>/Clcn2<tm1Mlv>	involves: C57BL/6	N	11976342
MGI:3850853	M	MP:0001152	increased Leydig cell number	Clcn2<tm1Mlv>/Clcn2<tm1Mlv>	involves: C57BL/6	N	11976342
MGI:3850853	M	MP:0005159	azoospermia	Clcn2<tm1Mlv>/Clcn2<tm1Mlv>	involves: C57BL/6	N	11976342
MGI:3850978	M	MP:0008280	abnormal male germ cell apoptosis	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	F	MP:0002682	decreased mature ovarian follicle number	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	M	MP:0001153	small seminiferous tubules	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	F	MP:0004834	ovary hemorrhage	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	M	MP:0004929	decreased epididymis weight	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	M	MP:0004852	decreased testis weight	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	F	MP:0001131	abnormal ovarian follicle morphology	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	F	MP:0001134	absent corpus luteum	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	M	MP:0005169	abnormal male meiosis	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	M	MP:0001147	small testis	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	M	MP:0001156	abnormal spermatogenesis	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	M	MP:0002687	oligozoospermia	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	F	MP:0006361	abnormal female germ cell morphology	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	F	MP:0005431	decreased oocyte number	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	F	MP:0001923	reduced female fertility	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3850978	F	MP:0009444	ovarian follicular cyst	Hsf2<tm1Mmr>/Hsf2<tm1Mmr>	involves: 129S2/SvPas * C57BL/6	N	12032072
MGI:3851105	M	MP:0000416	sparse hair	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0030651	decreased circulating ornithine level	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0001394	circling	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0001263	weight loss	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0003997	tonic-clonic seizures	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0002083	premature death	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0001265	decreased body size	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0001211	wrinkled skin	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0003415	priapism	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0020837	decreased circulating citrulline level	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0001431	abnormal eating behavior	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0030662	decreased circulating arginine level	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0030709	increased circulating glutamine level	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0001402	decreased locomotor activity	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0000745	tremors	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0011765	oroticaciduria	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0001442	decreased grooming behavior	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851105	M	MP:0005309	increased circulating ammonia level	Otc<spf>/Y	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851107	F	MP:0001923	reduced female fertility	Otc<spf>/Otc<+>	involves: C3H/HeJ * C57BL/6J	N	8750014
MGI:3851109	F	MP:0001386	abnormal maternal nurturing	vc/vc	DBA/1-vc	N	MGI:48835
MGI:3851110	F	MP:0001211	wrinkled skin	Otc<spf>/Otc<spf>	Not Specified	N	MGI:77872
MGI:3851110	F	MP:0001265	decreased body size	Otc<spf>/Otc<spf>	Not Specified	N	MGI:77872
MGI:3851110	F	MP:0000416	sparse hair	Otc<spf>/Otc<spf>	Not Specified	N	MGI:77872
MGI:3851110	F	MP:0001510	abnormal coat appearance	Otc<spf>/Otc<spf>	Not Specified	N	MGI:77872
MGI:3851179	F	MP:0011102	embryonic lethality, incomplete penetrance	Aifm1<tm2.1Pngr>/Aifm1<+>	involves: 129P2/OlaHsd * FVB/N	N	16788063
MGI:3851180	M	MP:0000774	decreased brain size	Aifm1<tm2.1Pngr>/Y	involves: 129P2/OlaHsd * FVB/N	N	16788063
MGI:3851180	M	MP:0011732	decreased somite size	Aifm1<tm2.1Pngr>/Y	involves: 129P2/OlaHsd * FVB/N	N	16788063
MGI:3851180	M	MP:0013504	increased embryonic tissue cell apoptosis	Aifm1<tm2.1Pngr>/Y	involves: 129P2/OlaHsd * FVB/N	N	16788063
MGI:3851180	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Aifm1<tm2.1Pngr>/Y	involves: 129P2/OlaHsd * FVB/N	N	16788063
MGI:3851180	M	MP:0001698	decreased embryo size	Aifm1<tm2.1Pngr>/Y	involves: 129P2/OlaHsd * FVB/N	N	16788063
MGI:3851180	M	MP:0010955	abnormal respiratory electron transport chain	Aifm1<tm2.1Pngr>/Y	involves: 129P2/OlaHsd * FVB/N	N	16788063
MGI:3851181	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Aifm1<tm2.1Pngr>/Aifm1<tm2.1Pngr>	involves: 129P2/OlaHsd * FVB/N	N	16788063
MGI:3851181	F	MP:0001698	decreased embryo size	Aifm1<tm2.1Pngr>/Aifm1<tm2.1Pngr>	involves: 129P2/OlaHsd * FVB/N	N	16788063
MGI:3851181	F	MP:0010955	abnormal respiratory electron transport chain	Aifm1<tm2.1Pngr>/Aifm1<tm2.1Pngr>	involves: 129P2/OlaHsd * FVB/N	N	16788063
MGI:3851181	F	MP:0013504	increased embryonic tissue cell apoptosis	Aifm1<tm2.1Pngr>/Aifm1<tm2.1Pngr>	involves: 129P2/OlaHsd * FVB/N	N	16788063
MGI:3851181	F	MP:0011732	decreased somite size	Aifm1<tm2.1Pngr>/Aifm1<tm2.1Pngr>	involves: 129P2/OlaHsd * FVB/N	N	16788063
MGI:3851181	F	MP:0000774	decreased brain size	Aifm1<tm2.1Pngr>/Aifm1<tm2.1Pngr>	involves: 129P2/OlaHsd * FVB/N	N	16788063
MGI:3851184	M	MP:0005621	abnormal cell physiology	Aifm1<tm1Pngr>/Y	129P2/OlaHsd-Aifm1<tm1Pngr>	N	11279485
MGI:3851207	F	MP:0009222	increased uterus tumor incidence	Msh6<tm1Htr>/Msh6<tm1Htr>	involves: 129P2/OlaHsd * FVB/N	N	10545954
MGI:3851227	M	MP:0001147	small testis	Oca2<p-25H>/Oca2<p-25H>	Not Specified	N	5565073
MGI:3851227	M	MP:0001940	testis hypoplasia	Oca2<p-25H>/Oca2<p-25H>	Not Specified	N	5565073
MGI:3851227	M	MP:0009233	enlarged sperm head	Oca2<p-25H>/Oca2<p-25H>	Not Specified	N	5565073
MGI:3851227	M	MP:0006380	abnormal spermatid morphology	Oca2<p-25H>/Oca2<p-25H>	Not Specified	N	5565073
MGI:3851227	M	MP:0001153	small seminiferous tubules	Oca2<p-25H>/Oca2<p-25H>	Not Specified	N	5565073
MGI:3851227	M	MP:0008892	abnormal sperm flagellum morphology	Oca2<p-25H>/Oca2<p-25H>	Not Specified	N	5565073
MGI:3851227	M	MP:0009230	abnormal sperm head morphology	Oca2<p-25H>/Oca2<p-25H>	Not Specified	N	5565073
MGI:3851227	F	MP:0001386	abnormal maternal nurturing	Oca2<p-25H>/Oca2<p-25H>	Not Specified	N	9689098
MGI:3851227	M	MP:0020550	multinucleated giant male germ cells	Oca2<p-25H>/Oca2<p-25H>	Not Specified	N	5565073
MGI:3851227	M	MP:0004901	decreased male germ cell number	Oca2<p-25H>/Oca2<p-25H>	Not Specified	N	5565073
MGI:3851227	M	MP:0008898	abnormal acrosome morphology	Oca2<p-25H>/Oca2<p-25H>	Not Specified	N	5565073
MGI:3851227	F	MP:0001384	abnormal pup retrieval	Oca2<p-25H>/Oca2<p-25H>	Not Specified	N	9689098
MGI:3851258	M	MP:0001764	abnormal homeostasis	Otc<spf-ash>/Y	involves: C57BL/6	N	7827141
MGI:3851258	M	MP:0005027	increased susceptibility to parasitic infection	Otc<spf-ash>/Y	involves: C57BL/6	N	7827141
MGI:3851258	M	MP:0009763	increased susceptibility to induced morbidity/mortality	Otc<spf-ash>/Y	involves: C57BL/6	N	7827141
MGI:3851258	M	MP:0011765	oroticaciduria	Otc<spf-ash>/Y	involves: C57BL/6	N	7827141
MGI:3851259	F	MP:0011765	oroticaciduria	Otc<spf-ash>/Otc<+>	involves: C57BL/6	N	7827141
MGI:3851329	M	MP:0001925	male infertility	B4galnt1<tm1Rlp>/B4galnt1<tm1Rlp>,St8sia1<tm1Rlp>/St8sia1<tm1Rlp>	involves: 129S6/SvEvTac	N	11133999
MGI:3851329	M	MP:0001156	abnormal spermatogenesis	B4galnt1<tm1Rlp>/B4galnt1<tm1Rlp>,St8sia1<tm1Rlp>/St8sia1<tm1Rlp>	involves: 129S6/SvEvTac	N	11133999
MGI:3851332	M	MP:0008735	increased susceptibility to endotoxin shock	Otc<spf-ash>/Y	B6EiC3Sn a/A-Otc<spf-ash>/J	N	16497529
MGI:3851332	M	MP:0008414	abnormal spatial reference memory	Otc<spf-ash>/Y	B6EiC3Sn a/A-Otc<spf-ash>/J	N	16497529
MGI:3851332	M	MP:0008428	abnormal spatial working memory	Otc<spf-ash>/Y	B6EiC3Sn a/A-Otc<spf-ash>/J	N	16497529
MGI:3851332	M	MP:0001265	decreased body size	Otc<spf-ash>/Y	B6EiC3Sn a/A-Otc<spf-ash>/J	N	16497529
MGI:3851332	M	MP:0001463	abnormal spatial learning	Otc<spf-ash>/Y	B6EiC3Sn a/A-Otc<spf-ash>/J	N	16497529
MGI:3851332	M	MP:0005309	increased circulating ammonia level	Otc<spf-ash>/Y	B6EiC3Sn a/A-Otc<spf-ash>/J	N	16497529
MGI:3851374	M	MP:0002286	cryptorchism	us/us	Not Specified	N	7906966
MGI:3851374	M	MP:0001147	small testis	us/us	Not Specified	N	7906966
MGI:3851374	M	MP:0001157	small seminal vesicle	us/us	Not Specified	N	7906966
MGI:3851374	F	MP:0002016	ovary cyst	us/us	Not Specified	N	7906966
MGI:3851374	M	MP:0031287	bilateral cryptorchism	us/us	Not Specified	N	7906966
MGI:3851374	F	MP:0001144	vagina atresia	us/us	Not Specified	N	7906966
MGI:3851374	F	MP:0001926	female infertility	us/us	Not Specified	N	7906966
MGI:3851374	M	MP:0001925	male infertility	us/us	Not Specified	N	7906966
MGI:3851374	M	MP:0031286	unilateral cryptorchism	us/us	Not Specified	N	7906966
MGI:3851509	F	MP:0011088	neonatal lethality, incomplete penetrance	Cnga2<tm1Gvr>/Cnga2<tm1Gvr>	involves: 129 * C57BL/6	N	9636130
MGI:3851509	F	MP:0001473	reduced long-term potentiation	Cnga2<tm1Gvr>/Cnga2<tm1Gvr>	involves: 129 * C57BL/6	N	9636130
MGI:3851509	F	MP:0002922	decreased post-tetanic potentiation	Cnga2<tm1Gvr>/Cnga2<tm1Gvr>	involves: 129 * C57BL/6	N	9636130
MGI:3851510	M	MP:0002922	decreased post-tetanic potentiation	Cnga2<tm1Gvr>/Y	involves: 129 * C57BL/6	N	9636130
MGI:3851510	M	MP:0001473	reduced long-term potentiation	Cnga2<tm1Gvr>/Y	involves: 129 * C57BL/6	N	9636130
MGI:3851510	M	MP:0011088	neonatal lethality, incomplete penetrance	Cnga2<tm1Gvr>/Y	involves: 129 * C57BL/6	N	9636130
MGI:3851516	M	MP:0000819	abnormal olfactory bulb morphology	Cnga2<tm1Gvr>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	10531436
MGI:3851516	M	MP:0002741	small olfactory bulb	Cnga2<tm1Gvr>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	10531436
MGI:3851516	M	MP:0011088	neonatal lethality, incomplete penetrance	Cnga2<tm1Gvr>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	10531436
MGI:3851516	M	MP:0005236	abnormal olfactory nerve morphology	Cnga2<tm1Gvr>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	10531436
MGI:3851530	F	MP:0009504	abnormal mammary gland epithelium morphology	Stat6<tm1Gru>/Stat6<tm1Gru>	involves: 129S2/SvPas	N	22588720
MGI:3851530	F	MP:0006269	abnormal mammary gland growth during pregnancy	Stat6<tm1Gru>/Stat6<tm1Gru>	involves: 129S2/SvPas	N	22588720
MGI:3851530	F	MP:0000627	abnormal mammary gland morphology	Stat6<tm1Gru>/Stat6<tm1Gru>	involves: 129S2/SvPas	N	22588720
MGI:3851530	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Stat6<tm1Gru>/Stat6<tm1Gru>	involves: 129S2/SvPas	N	22588720
MGI:3851594	M	MP:0004884	abnormal testis physiology	Acsbg1<tm1Mld>/Acsbg1<tm1Mld>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	19167491
MGI:3851594	M	MP:0002786	abnormal Leydig cell morphology	Acsbg1<tm1Mld>/Acsbg1<tm1Mld>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	19167491
MGI:3851597	M	MP:0003887	increased hepatocyte apoptosis	Ikbkg<tm1Mak>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10766741
MGI:3851597	M	MP:0003888	liver hemorrhage	Ikbkg<tm1Mak>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10766741
MGI:3851597	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Ikbkg<tm1Mak>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10766741
MGI:3851597	M	MP:0008705	increased interleukin-6 secretion	Ikbkg<tm1Mak>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10766741
MGI:3851597	M	MP:0013501	increased fibroblast apoptosis	Ikbkg<tm1Mak>/Y	involves: 129P2/OlaHsd * C57BL/6	N	10766741
MGI:3851610	M	MP:0006378	abnormal spermatogonia morphology	Dmrt1<tm1Zark>/Dmrt1<tm1.1Zark>,Tg(Dhh-cre)1Mejr/0	involves: 129/Sv * C57BL/6	N	17540358
MGI:3851610	M	MP:0003830	abnormal testis development	Dmrt1<tm1Zark>/Dmrt1<tm1.1Zark>,Tg(Dhh-cre)1Mejr/0	involves: 129/Sv * C57BL/6	N	17540358
MGI:3851610	M	MP:0004109	abnormal Sertoli cell development	Dmrt1<tm1Zark>/Dmrt1<tm1.1Zark>,Tg(Dhh-cre)1Mejr/0	involves: 129/Sv * C57BL/6	N	17540358
MGI:3851611	M	MP:0006378	abnormal spermatogonia morphology	Alpl<tm1(cre)Nagy>/Alpl<+>,Dmrt1<tm1Zark>/Dmrt1<tm1.1Zark>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17540358
MGI:3851611	M	MP:0004901	decreased male germ cell number	Alpl<tm1(cre)Nagy>/Alpl<+>,Dmrt1<tm1Zark>/Dmrt1<tm1.1Zark>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17540358
MGI:3851611	M	MP:0003830	abnormal testis development	Alpl<tm1(cre)Nagy>/Alpl<+>,Dmrt1<tm1Zark>/Dmrt1<tm1.1Zark>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	17540358
MGI:3851695	M	MP:0008215	decreased immature B cell number	Cd19<tm1(cre)Cgn>/Cd19<+>,Ikbkg<tm1.1Mpa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12235208
MGI:3851695	M	MP:0005154	increased B cell proliferation	Cd19<tm1(cre)Cgn>/Cd19<+>,Ikbkg<tm1.1Mpa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12235208
MGI:3851695	M	MP:0004978	decreased B-1 B cell number	Cd19<tm1(cre)Cgn>/Cd19<+>,Ikbkg<tm1.1Mpa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12235208
MGI:3851695	M	MP:0008174	decreased follicular B cell number	Cd19<tm1(cre)Cgn>/Cd19<+>,Ikbkg<tm1.1Mpa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12235208
MGI:3851695	M	MP:0008211	decreased mature B cell number	Cd19<tm1(cre)Cgn>/Cd19<+>,Ikbkg<tm1.1Mpa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12235208
MGI:3851695	M	MP:0008182	decreased marginal zone B cell number	Cd19<tm1(cre)Cgn>/Cd19<+>,Ikbkg<tm1.1Mpa>/Y	involves: 129P2/OlaHsd * C57BL/6	N	12235208
MGI:3851809	M	MP:0001146	abnormal testis morphology	Pex5<tm1Pec>/Pex5<tm1Pec>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3851809	M	MP:0001925	male infertility	Pex5<tm1Pec>/Pex5<tm1Pec>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3851809	M	MP:0002216	abnormal seminiferous tubule morphology	Pex5<tm1Pec>/Pex5<tm1Pec>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3851809	M	MP:0004852	decreased testis weight	Pex5<tm1Pec>/Pex5<tm1Pec>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3851809	M	MP:0001154	seminiferous tubule degeneration	Pex5<tm1Pec>/Pex5<tm1Pec>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ	N	16484321
MGI:3851910	M	MP:0008276	failure of intramembranous bone ossification	Hdac8<tm1.2Eno>/Y	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851910	M	MP:0004378	frontal bone foramen	Hdac8<tm1.2Eno>/Y	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851910	M	MP:0000914	exencephaly	Hdac8<tm1.2Eno>/Y	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851910	M	MP:0011087	neonatal lethality, complete penetrance	Hdac8<tm1.2Eno>/Y	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851910	M	MP:0009429	decreased embryo weight	Hdac8<tm1.2Eno>/Y	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851910	M	MP:0011088	neonatal lethality, incomplete penetrance	Hdac8<tm1.2Eno>/Y	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851910	M	MP:0001915	intracranial hemorrhage	Hdac8<tm1.2Eno>/Y	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851911	F	MP:0000914	exencephaly	Hdac8<tm1.2Eno>/Hdac8<tm1.2Eno>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851911	F	MP:0008276	failure of intramembranous bone ossification	Hdac8<tm1.2Eno>/Hdac8<tm1.2Eno>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851911	F	MP:0004378	frontal bone foramen	Hdac8<tm1.2Eno>/Hdac8<tm1.2Eno>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851911	F	MP:0011088	neonatal lethality, incomplete penetrance	Hdac8<tm1.2Eno>/Hdac8<tm1.2Eno>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851911	F	MP:0001915	intracranial hemorrhage	Hdac8<tm1.2Eno>/Hdac8<tm1.2Eno>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851911	F	MP:0009429	decreased embryo weight	Hdac8<tm1.2Eno>/Hdac8<tm1.2Eno>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851911	F	MP:0011087	neonatal lethality, complete penetrance	Hdac8<tm1.2Eno>/Hdac8<tm1.2Eno>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851912	F	MP:0001915	intracranial hemorrhage	Hdac8<tm1.2Eno>/Hdac8<+>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851912	F	MP:0003121	genetic imprinting	Hdac8<tm1.2Eno>/Hdac8<+>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851912	F	MP:0011088	neonatal lethality, incomplete penetrance	Hdac8<tm1.2Eno>/Hdac8<+>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851912	F	MP:0009429	decreased embryo weight	Hdac8<tm1.2Eno>/Hdac8<+>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851912	F	MP:0000914	exencephaly	Hdac8<tm1.2Eno>/Hdac8<+>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851912	F	MP:0008276	failure of intramembranous bone ossification	Hdac8<tm1.2Eno>/Hdac8<+>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851912	F	MP:0004378	frontal bone foramen	Hdac8<tm1.2Eno>/Hdac8<+>	involves: 129 * C57BL/6 * CD-1	N	19605684
MGI:3851913	F	MP:0002169	no abnormal phenotype detected	Hdac8<tm1.2Eno>/Hdac8<+>,Tg(CAG-Hdac8,-EGFP)1Eno/0	involves: 129 * C57BL/6 * C3H * CD-1	N	19605684
MGI:3851915	M	MP:0002169	no abnormal phenotype detected	Hdac8<tm1.1Eno>/Y,Tg(Col1a1-cre)1Kry/0	involves: 129 * C57BL/6 * CD-1 * FVB/N	N	19605684
MGI:3851916	M	MP:0002169	no abnormal phenotype detected	Hdac8<tm1.1Eno>/Y,Tg(Col2a1-cre)1Bhr/0	involves: 129 * C57BL/6 * CD-1 * SJL	N	19605684
MGI:3851917	M	MP:0002169	no abnormal phenotype detected	Hdac8<tm1.1Eno>/Y,Twist2<tm1(cre)Dor>/Twist2<+>	involves: 129 * C57BL/6 * CD-1 * SJL	N	19605684
MGI:3851920	M	MP:0004378	frontal bone foramen	Hdac8<tm1.1Eno>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129 * C57BL/6 * CBA * CD-1	N	19605684
MGI:3851920	M	MP:0008276	failure of intramembranous bone ossification	Hdac8<tm1.1Eno>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129 * C57BL/6 * CBA * CD-1	N	19605684
MGI:3851920	M	MP:0001915	intracranial hemorrhage	Hdac8<tm1.1Eno>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129 * C57BL/6 * CBA * CD-1	N	19605684
MGI:3851920	M	MP:0011088	neonatal lethality, incomplete penetrance	Hdac8<tm1.1Eno>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129 * C57BL/6 * CBA * CD-1	N	19605684
MGI:3851991	F	MP:0008000	increased ovary tumor incidence	Stk11<tm1Mmt>/Stk11<+>,Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd * 129X1/SvJ	N	16278673
MGI:3852169	M	MP:0001922	reduced male fertility	Lum<tm1Wwk>/Lum<tm1Wwk>	involves: 129P2/OlaHsd * C57BL/6J	N	10644720
MGI:3852485	F	MP:0006271	abnormal involution of the mammary gland	Ptprf<tm1Wjh>/Ptprf<tm1Wjh>	involves: 129P2/OlaHsd * C57BL/6	N	9245518
MGI:3852485	F	MP:0003838	abnormal milk ejection	Ptprf<tm1Wjh>/Ptprf<tm1Wjh>	involves: 129P2/OlaHsd * C57BL/6	N	9245518
MGI:3852485	F	MP:0009506	abnormal mammary gland alveolus morphology	Ptprf<tm1Wjh>/Ptprf<tm1Wjh>	involves: 129P2/OlaHsd * C57BL/6	N	9245518
MGI:4352948	F	MP:0001926	female infertility	Antxr2<tm1.2Lepp>/Antxr2<tm1.2Lepp>	involves: C57BL/6	N	19617532
MGI:4352949	F	MP:0001926	female infertility	Antxr1<tm1.2Lepp>/Antxr1<tm1.2Lepp>	involves: 129 * C57BL/6	N	19617532
MGI:4353024	F	MP:0003932	abnormal molar crown morphology	Eda<Ta>/Eda<+>,Edaradd<cr>/Edaradd<+>	involves: JU/Fa	N	478295
MGI:4353024	F	MP:0006402	small molars	Eda<Ta>/Eda<+>,Edaradd<cr>/Edaradd<+>	involves: JU/Fa	N	478295
MGI:4353039	M	MP:0005389	reproductive system phenotype	X/In(YLS)Lub	Not Specified	Y	MGI:3846454
MGI:4353039	M	MP:0003702	abnormal chromosome morphology	X/In(YLS)Lub	Not Specified	N	MGI:3846454
MGI:4353101	M	MP:0002169	no abnormal phenotype detected	X/Tg(Pomc-FLP)1bBrn	involves: FVB/N	N	9671308
MGI:4353104	M	MP:0008371	pituitary intermediate lobe hyperplasia	Rb1<tm1Brn>/Rb1<tm1Brn>,X/Tg(Pomc-FLP)1bBrn	involves: 129P2/OlaHsd * FVB/N	N	9671308
MGI:4353104	M	MP:0014237	decreased tumor-free survival time	Rb1<tm1Brn>/Rb1<tm1Brn>,X/Tg(Pomc-FLP)1bBrn	involves: 129P2/OlaHsd * FVB/N	N	9671308
MGI:4353104	M	MP:0002041	increased pituitary adenoma incidence	Rb1<tm1Brn>/Rb1<tm1Brn>,X/Tg(Pomc-FLP)1bBrn	involves: 129P2/OlaHsd * FVB/N	N	9671308
MGI:4353105	M	MP:0008371	pituitary intermediate lobe hyperplasia	Rb1<tm1Brn>/Rb1<+>,X/Tg(Pomc-FLP)1bBrn	involves: 129P2/OlaHsd * FVB/N	N	9671308
MGI:4353223	M	MP:0001364	decreased anxiety-related response	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0003863	decreased aggression towards mice	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0000243	myoclonus	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0003858	enhanced coordination	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0003998	decreased thermal nociceptive threshold	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0003997	tonic-clonic seizures	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0009456	impaired cued conditioning behavior	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0003996	clonic seizures	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0002064	seizures	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0000859	abnormal somatosensory cortex morphology	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0002062	abnormal associative learning	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0008269	abnormal hippocampus CA4 region morphology	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0004101	abnormal brain interneuron morphology	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0000788	abnormal cerebral cortex morphology	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0004077	abnormal striatum morphology	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0004994	abnormal brain wave pattern	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0009454	impaired contextual conditioning behavior	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353223	M	MP:0005379	endocrine/exocrine gland phenotype	Arx<tm1.1Jno>/Y	involves: 129S7/SvEvBrd * C57BL/6J	Y	19587282
MGI:4353224	F	MP:0005379	endocrine/exocrine gland phenotype	Arx<tm1.1Jno>/Arx<tm1.1Jno>	involves: 129S7/SvEvBrd * C57BL/6J	Y	19587282
MGI:4353224	F	MP:0000243	myoclonus	Arx<tm1.1Jno>/Arx<tm1.1Jno>	involves: 129S7/SvEvBrd * C57BL/6J	N	19587282
MGI:4353403	F	MP:0001126	abnormal ovary morphology	Antxr1<tm1.2Bstc>/Antxr1<tm1.2Bstc>	B6.Cg-Antxr1<tm1.2Bstc>	N	19622764
MGI:4353418	M	MP:0001925	male infertility	Pi4k2a<Gt(AK0094)Wtsi>/Pi4k2a<Gt(AK0094)Wtsi>	involves: 129P2/OlaHsd * BALB/c	N	19581584
MGI:4353418	F	MP:0001923	reduced female fertility	Pi4k2a<Gt(AK0094)Wtsi>/Pi4k2a<Gt(AK0094)Wtsi>	involves: 129P2/OlaHsd * BALB/c	N	19581584
MGI:4353654	F	MP:0009456	impaired cued conditioning behavior	Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	B6.Cg-Nlgn3<tm1Bros>	N	19243448
MGI:4353654	F	MP:0000774	decreased brain size	Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	B6.Cg-Nlgn3<tm1Bros>	N	19243448
MGI:4353654	F	MP:0001360	abnormal social investigation	Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	B6.Cg-Nlgn3<tm1Bros>	N	19243448
MGI:4353654	F	MP:0005386	behavior/neurological phenotype	Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	B6.Cg-Nlgn3<tm1Bros>	Y	19243448
MGI:4353654	F	MP:0003631	nervous system phenotype	Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	B6.Cg-Nlgn3<tm1Bros>	Y	19243448
MGI:4353654	F	MP:0009454	impaired contextual conditioning behavior	Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	B6.Cg-Nlgn3<tm1Bros>	N	19243448
MGI:4353654	F	MP:0001415	increased exploration in new environment	Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	B6.Cg-Nlgn3<tm1Bros>	N	19243448
MGI:4353654	F	MP:0008544	impaired olfaction	Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	B6.Cg-Nlgn3<tm1Bros>	N	19243448
MGI:4353654	F	MP:0020351	decreased vocalization	Nlgn3<tm1Bros>/Nlgn3<tm1Bros>	B6.Cg-Nlgn3<tm1Bros>	N	19243448
MGI:4353813	M	MP:0001925	male infertility	Dab1<scm>/Dab1<scm>	involves: C3HeB/FeJ * DC/Le	N	8875886
MGI:4353906	F	MP:0004047	abnormal milk composition	Jchain<tm1Jse>/Jchain<tm1Jse>	involves: 129X1/SvJ	N	8752925
MGI:4354283	F	MP:0001885	mammary gland duct hyperplasia	Rb1<tm2.1Jyjw>/Rb1<tm2.1Jyjw>	involves: 129 * C57BL/6	N	19506017
MGI:4354283	F	MP:0000630	mammary gland hyperplasia	Rb1<tm2.1Jyjw>/Rb1<tm2.1Jyjw>	involves: 129 * C57BL/6	N	19506017
MGI:4354283	F	MP:0003838	abnormal milk ejection	Rb1<tm2.1Jyjw>/Rb1<tm2.1Jyjw>	involves: 129 * C57BL/6	N	19506017
MGI:4354285	F	MP:0000630	mammary gland hyperplasia	Rb1<tm1Fad>/Rb1<tm1Fad>,Tg(MMTVTGFB1)46Hlm/?	involves: 129 * C57BL/6 * DBA/2	N	19506017
MGI:4354411	F	MP:0001120	abnormal uterus morphology	Cd44<tm2Kmz>/Cd44<tm2Kmz>	DBA/1LacJ-Cd44<tm2Kmz>	N	11825873
MGI:4354411	F	MP:0006271	abnormal involution of the mammary gland	Cd44<tm2Kmz>/Cd44<tm2Kmz>	DBA/1LacJ-Cd44<tm2Kmz>	N	11825873
MGI:4355020	F	MP:0004856	decreased ovary weight	Atr<tm1Ofc>/Atr<tm1Ofc>	Not Specified	N	19620979
MGI:4355020	F	MP:0009362	abnormal primary ovarian follicle morphology	Atr<tm1Ofc>/Atr<tm1Ofc>	Not Specified	N	19620979
MGI:4355020	M	MP:0004852	decreased testis weight	Atr<tm1Ofc>/Atr<tm1Ofc>	Not Specified	N	19620979
MGI:4355020	F	MP:0004805	absent oocytes	Atr<tm1Ofc>/Atr<tm1Ofc>	Not Specified	N	19620979
MGI:4355020	F	MP:0001931	abnormal oogenesis	Atr<tm1Ofc>/Atr<tm1Ofc>	Not Specified	N	19620979
MGI:4355046	M	MP:0001922	reduced male fertility	Adam17<tm1.2Bbl>/Adam17<tm1.2Bbl>,Sox9<tm3(cre)Crm>/Sox9<+>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	N	19201862
MGI:4355046	F	MP:0001926	female infertility	Adam17<tm1.2Bbl>/Adam17<tm1.2Bbl>,Sox9<tm3(cre)Crm>/Sox9<+>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	N	19201862
MGI:4355343	M	MP:0006086	decreased body mass index	Prep<Gt(RRM213)Byg>/Prep<Gt(RRM213)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19564876
MGI:4355343	F	MP:0003918	decreased kidney weight	Prep<Gt(RRM213)Byg>/Prep<Gt(RRM213)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19564876
MGI:4355343	F	MP:0005669	increased circulating leptin level	Prep<Gt(RRM213)Byg>/Prep<Gt(RRM213)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19564876
MGI:4355568	M	MP:0006378	abnormal spermatogonia morphology	Fancm<tm1.1Htr>/Fancm<tm1.1Htr>	involves: C57BL/6 * FVB	N	19561169
MGI:4355568	M	MP:0005159	azoospermia	Fancm<tm1.1Htr>/Fancm<tm1.1Htr>	involves: C57BL/6 * FVB	N	19561169
MGI:4355568	F	MP:0002682	decreased mature ovarian follicle number	Fancm<tm1.1Htr>/Fancm<tm1.1Htr>	involves: C57BL/6 * FVB	N	19561169
MGI:4355568	F	MP:0001126	abnormal ovary morphology	Fancm<tm1.1Htr>/Fancm<tm1.1Htr>	involves: C57BL/6 * FVB	N	19561169
MGI:4355568	M	MP:0002216	abnormal seminiferous tubule morphology	Fancm<tm1.1Htr>/Fancm<tm1.1Htr>	involves: C57BL/6 * FVB	N	19561169
MGI:4355568	M	MP:0001147	small testis	Fancm<tm1.1Htr>/Fancm<tm1.1Htr>	involves: C57BL/6 * FVB	N	19561169
MGI:4355568	M	MP:0001152	increased Leydig cell number	Fancm<tm1.1Htr>/Fancm<tm1.1Htr>	involves: C57BL/6 * FVB	N	19561169
MGI:4355581	M	MP:0002687	oligozoospermia	Galnt3<tm1Mjec>/Galnt3<tm1Mjec>	involves: 129S/SvEv * C57BL/6J	N	19213845
MGI:4355581	M	MP:0005578	teratozoospermia	Galnt3<tm1Mjec>/Galnt3<tm1Mjec>	involves: 129S/SvEv * C57BL/6J	N	19213845
MGI:4355581	M	MP:0001153	small seminiferous tubules	Galnt3<tm1Mjec>/Galnt3<tm1Mjec>	involves: 129S/SvEv * C57BL/6J	N	19213845
MGI:4355581	M	MP:0001925	male infertility	Galnt3<tm1Mjec>/Galnt3<tm1Mjec>	involves: 129S/SvEv * C57BL/6J	N	19213845
MGI:4355726	F	MP:0008042	abnormal NK T cell physiology	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0001860	liver inflammation	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0003887	increased hepatocyte apoptosis	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0002981	increased liver weight	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0008045	decreased NK cell number	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0008040	decreased NK T cell number	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0002941	increased circulating alanine transaminase level	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0001654	hepatic necrosis	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0002628	hepatic steatosis	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0008553	increased circulating tumor necrosis factor level	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0008566	increased interferon-gamma secretion	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0008873	increased physiological sensitivity to xenobiotic	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0003331	increased hepatocellular carcinoma incidence	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0010766	abnormal NK cell physiology	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355726	F	MP:0000598	abnormal liver morphology	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355727	F	MP:0002169	no abnormal phenotype detected	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>	involves: C57BL/6 * SJL	N	19635861
MGI:4355749	F	MP:0005501	abnormal skin physiology	Trex2<tm1.2Coso>/Trex2<tm1.2Coso>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	19654293
MGI:4355749	F	MP:0003453	abnormal keratinocyte physiology	Trex2<tm1.2Coso>/Trex2<tm1.2Coso>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	19654293
MGI:4355749	F	MP:0009581	decreased keratinocyte apoptosis	Trex2<tm1.2Coso>/Trex2<tm1.2Coso>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	19654293
MGI:4355749	F	MP:0004499	increased incidence of tumors by chemical induction	Trex2<tm1.2Coso>/Trex2<tm1.2Coso>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	19654293
MGI:4355750	M	MP:0005501	abnormal skin physiology	Trex2<tm1.2Coso>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	19654293
MGI:4355750	M	MP:0004499	increased incidence of tumors by chemical induction	Trex2<tm1.2Coso>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	19654293
MGI:4355750	M	MP:0003453	abnormal keratinocyte physiology	Trex2<tm1.2Coso>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	19654293
MGI:4355750	M	MP:0009581	decreased keratinocyte apoptosis	Trex2<tm1.2Coso>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	19654293
MGI:4355843	M	MP:0002981	increased liver weight	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0002941	increased circulating alanine transaminase level	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0003887	increased hepatocyte apoptosis	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0008874	decreased physiological sensitivity to xenobiotic	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0008045	decreased NK cell number	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0008042	abnormal NK T cell physiology	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0008040	decreased NK T cell number	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0003331	increased hepatocellular carcinoma incidence	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0002628	hepatic steatosis	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0008566	increased interferon-gamma secretion	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0003638	abnormal response/metabolism to endogenous compounds	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0001860	liver inflammation	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0000598	abnormal liver morphology	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355843	M	MP:0010766	abnormal NK cell physiology	Ikbkg<tm1.1Chtr>/Y,Tg(Alb1-cre)7Gsc/0	involves: C57BL/6 * FVB/N * SJL	N	19635861
MGI:4355886	F	MP:0009724	ectopic nipples	Nrg3<ska>/Nrg3<ska>	A/J	N	10723730
MGI:4355886	F	MP:0009741	ectopic mammary gland	Nrg3<ska>/Nrg3<ska>	A/J	N	10723730
MGI:4355886	F	MP:0000628	abnormal mammary gland development	Nrg3<ska>/Nrg3<ska>	A/J	N	10723730
MGI:4355886	F	MP:0009721	increased mammary gland number	Nrg3<ska>/Nrg3<ska>	A/J	N	10723730
MGI:4355886	F	MP:0000629	absent mammary gland	Nrg3<ska>/Nrg3<ska>	A/J	N	10723730
MGI:4355886	F	MP:0009722	abnormal nipple development	Nrg3<ska>/Nrg3<ska>	A/J	N	10723730
MGI:4355886	F	MP:0009720	abnormal mammary gland pattern	Nrg3<ska>/Nrg3<ska>	A/J	N	10723730
MGI:4355886	F	MP:0009723	increased nipple number	Nrg3<ska>/Nrg3<ska>	A/J	N	10723730
MGI:4356292	F	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Tg(CD2-Ccdc86)1Hfuj/?	B6.Cg-Il2rg<tm1Wjl> Tg(CD2-Ccdc86)1Hfuj	N	19528538
MGI:4356292	F	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Tg(CD2-Ccdc86)1Hfuj/?	B6.Cg-Il2rg<tm1Wjl> Tg(CD2-Ccdc86)1Hfuj	N	19528538
MGI:4356292	F	MP:0005387	immune system phenotype	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Tg(CD2-Ccdc86)1Hfuj/?	B6.Cg-Il2rg<tm1Wjl> Tg(CD2-Ccdc86)1Hfuj	Y	19528538
MGI:4356292	F	MP:0004974	decreased regulatory T cell number	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Tg(CD2-Ccdc86)1Hfuj/?	B6.Cg-Il2rg<tm1Wjl> Tg(CD2-Ccdc86)1Hfuj	N	19528538
MGI:4356292	F	MP:0009339	decreased splenocyte number	Il2rg<tm1Wjl>/Il2rg<tm1Wjl>,Tg(CD2-Ccdc86)1Hfuj/?	B6.Cg-Il2rg<tm1Wjl> Tg(CD2-Ccdc86)1Hfuj	N	19528538
MGI:4356437	M	MP:0011939	increased food intake	Del(7Ipw-Snord116)1Jbro/+	involves: 129S7/SvEvBrd * C57BL/6	N	27672097
MGI:4356437	M	MP:0001431	abnormal eating behavior	Del(7Ipw-Snord116)1Jbro/+	involves: 129S7/SvEvBrd * C57BL/6	N	27672097
MGI:4356437	M	MP:0004924	abnormal behavior	Del(7Ipw-Snord116)1Jbro/+	involves: 129S7/SvEvBrd * C57BL/6	N	27672097
MGI:4356438	M	MP:0011939	increased food intake	Del(7Ipw-Snord116)1Jbro/Del(7Ipw-Snord116)1Jbro	involves: 129S7/SvEvBrd * C57BL/6	N	27672097
MGI:4356438	M	MP:0001431	abnormal eating behavior	Del(7Ipw-Snord116)1Jbro/Del(7Ipw-Snord116)1Jbro	involves: 129S7/SvEvBrd * C57BL/6	N	27672097
MGI:4356438	M	MP:0004924	abnormal behavior	Del(7Ipw-Snord116)1Jbro/Del(7Ipw-Snord116)1Jbro	involves: 129S7/SvEvBrd * C57BL/6	N	27672097
MGI:4356528	F	MP:0001926	female infertility	Mitf<Mi-Or>/Mitf<Mi-Or>	involves: 101/Rl * C3H/Rl	N	MGI:61619
MGI:4357778	M	MP:0004852	decreased testis weight	Asz1<tm1Zuk>/Asz1<tm1Zuk>	involves: 129 * C57BL/6	N	19730684
MGI:4357778	M	MP:0006379	abnormal spermatocyte morphology	Asz1<tm1Zuk>/Asz1<tm1Zuk>	involves: 129 * C57BL/6	N	19730684
MGI:4357778	M	MP:0001925	male infertility	Asz1<tm1Zuk>/Asz1<tm1Zuk>	involves: 129 * C57BL/6	N	19730684
MGI:4357778	M	MP:0001155	arrest of spermatogenesis	Asz1<tm1Zuk>/Asz1<tm1Zuk>	involves: 129 * C57BL/6	N	19730684
MGI:4357778	M	MP:0005169	abnormal male meiosis	Asz1<tm1Zuk>/Asz1<tm1Zuk>	involves: 129 * C57BL/6	N	19730684
MGI:4357789	M	MP:0001147	small testis	Hdac2<Gt(W035F03)Joe>/Hdac2<Gt(W035F03)Joe>	involves: 129S2/SvPas	N	17909008
MGI:4357858	M	MP:0005377	hearing/vestibular/ear phenotype	Cldn9<nmf329>/Cldn9<nmf329>,Pou3f4<del-J>/Y	involves: C3HeB/FeJ * C57BL/6J	Y	19696885
MGI:4357931	M	MP:0010768	mortality/aging	Gck<Gls006>/Gck<Gls006>	C3HeB/FeJ-Gck<Gls006>	Y	22698525
MGI:4357931	M	MP:0009114	decreased pancreatic beta cell mass	Gck<Gls006>/Gck<Gls006>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:4357931	M	MP:0005215	abnormal pancreatic islet morphology	Gck<Gls006>/Gck<Gls006>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:4357931	M	MP:0005559	increased circulating glucose level	Gck<Gls006>/Gck<Gls006>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:4357931	M	MP:0001262	decreased body weight	Gck<Gls006>/Gck<Gls006>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:4357931	M	MP:0009172	small pancreatic islets	Gck<Gls006>/Gck<Gls006>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:4357931	M	MP:0005217	abnormal pancreatic beta cell morphology	Gck<Gls006>/Gck<Gls006>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:4357931	M	MP:0001559	hyperglycemia	Gck<Gls006>/Gck<Gls006>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:4358248	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-ERG*)1Vv/0	involves: 129/Sv * C57BL/6J * CBA	N	18245377
MGI:4358248	M	MP:0001168	abnormal prostate gland epithelium morphology	Tg(Pbsn-ERG*)1Vv/0	involves: 129/Sv * C57BL/6J * CBA	N	18245377
MGI:4358249	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	30401749
MGI:4358249	M	MP:0002038	increased carcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	30401749
MGI:4358249	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	23512661
MGI:4358249	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	30401749
MGI:4358249	M	MP:0000659	prostate gland hyperplasia	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21493594
MGI:4358249	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	30401749
MGI:4358249	M	MP:0010768	mortality/aging	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	Y	23512661
MGI:4358249	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22350410
MGI:4358249	M	MP:0004961	increased prostate gland weight	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21493594
MGI:4358249	M	MP:0009738	enlarged prostate gland anterior lobe	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21493594
MGI:4358249	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	18245377
MGI:4358249	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	23512661
MGI:4358249	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21493594
MGI:4358249	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21620777
MGI:4358249	M	MP:0001272	increased metastatic potential	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	30401749
MGI:4358251	F	MP:0005431	decreased oocyte number	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	M	MP:0001156	abnormal spermatogenesis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	F	MP:0001127	small ovary	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	M	MP:0001155	arrest of spermatogenesis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	M	MP:0001153	small seminiferous tubules	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	F	MP:0001926	female infertility	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	M	MP:0001925	male infertility	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	F	MP:0011121	decreased primordial ovarian follicle number	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	M	MP:0004852	decreased testis weight	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	M	MP:0005159	azoospermia	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	F	MP:0001126	abnormal ovary morphology	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	F	MP:0001931	abnormal oogenesis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	M	MP:0005169	abnormal male meiosis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	F	MP:0005168	abnormal female meiosis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	F	MP:0001129	impaired ovarian folliculogenesis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358251	M	MP:0006380	abnormal spermatid morphology	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6	N	11106739
MGI:4358381	M	MP:0002685	abnormal spermatogonia proliferation	fpw/fpw	involves: C3H/HeJ * C57BL/6J	N	19513787
MGI:4358483	M	MP:0001155	arrest of spermatogenesis	Kit<tm1.1Bsm>/Kit<tm1.1Bsm>	B6.129S1-Kit<tm1.1Bsm>	N	15024050
MGI:4358484	F	MP:0001825	arrested T cell differentiation	Il2rg<tm1Cgn>/Il2rg<tm1Cgn>,Kit<tm1.1Bsm>/Kit<tm1.1Bsm>	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	N	15024050
MGI:4358494	M	MP:0001922	reduced male fertility	Cacna2d2<du>/Cacna2d2<du>	involves: DBA/2J	N	MGI:48656
MGI:4358494	F	MP:0001923	reduced female fertility	Cacna2d2<du>/Cacna2d2<du>	involves: DBA/2J	N	MGI:48656
MGI:4358594	M	MP:0001158	abnormal prostate gland morphology	Tg(Pbsn-Hpn,-GFP)DVv/0	involves: C57BL/6J * CBA	N	15324701
MGI:4358595	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(Pbsn-Hpn,-GFP)DVv/0,Tg(Pbsn-Tag)12T7fRjm/0	involves: C57BL/6J * CBA * CD-1	N	15324701
MGI:4358595	M	MP:0001158	abnormal prostate gland morphology	Tg(Pbsn-Hpn,-GFP)DVv/0,Tg(Pbsn-Tag)12T7fRjm/0	involves: C57BL/6J * CBA * CD-1	N	15324701
MGI:4358595	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-Hpn,-GFP)DVv/0,Tg(Pbsn-Tag)12T7fRjm/0	involves: C57BL/6J * CBA * CD-1	N	15324701
MGI:4358595	M	MP:0004958	enlarged prostate gland	Tg(Pbsn-Hpn,-GFP)DVv/0,Tg(Pbsn-Tag)12T7fRjm/0	involves: C57BL/6J * CBA * CD-1	N	15324701
MGI:4358596	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-Tag)12T7fRjm/0	involves: CD-1	N	9645768
MGI:4358596	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(Pbsn-Tag)12T7fRjm/0	involves: CD-1	N	9645768
MGI:4358596	M	MP:0010357	increased prostate gland tumor incidence	Tg(Pbsn-Tag)12T7fRjm/0	involves: CD-1	N	9645768
MGI:4358596	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-Tag)12T7fRjm/0	involves: CD-1	N	15324701
MGI:4358596	M	MP:0004958	enlarged prostate gland	Tg(Pbsn-Tag)12T7fRjm/0	involves: CD-1	N	15324701
MGI:4358596	M	MP:0001158	abnormal prostate gland morphology	Tg(Pbsn-Tag)12T7fRjm/0	involves: CD-1	N	15324701
MGI:4358596	M	MP:0000659	prostate gland hyperplasia	Tg(Pbsn-Tag)12T7fRjm/0	involves: CD-1	N	9645768
MGI:4358724	M	MP:0014365	impaired short-term object recognition memory	Dtnbp1<sdy>/Dtnbp1<sdy>	DBA/2J-Dtnbp1<sdy>/J	N	18984010
MGI:4358724	M	MP:0013894	abnormal behavioral response to amphetamine	Dtnbp1<sdy>/Dtnbp1<sdy>	DBA/2J-Dtnbp1<sdy>/J	N	18984010
MGI:4358724	M	MP:0011620	abnormal habituation to a new environment	Dtnbp1<sdy>/Dtnbp1<sdy>	DBA/2J-Dtnbp1<sdy>/J	N	18984010
MGI:4358724	M	MP:0003043	hypoalgesia	Dtnbp1<sdy>/Dtnbp1<sdy>	DBA/2J-Dtnbp1<sdy>/J	N	18984010
MGI:4358724	M	MP:0009455	enhanced cued conditioning behavior	Dtnbp1<sdy>/Dtnbp1<sdy>	DBA/2J-Dtnbp1<sdy>/J	N	18984010
MGI:4358749	F	MP:0001923	reduced female fertility	Pla2g4a<tm1Jvb>/Pla2g4a<tm1Jvb>	involves: 129S4/SvJae	N	9403693
MGI:4358795	F	MP:0002016	ovary cyst	Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	19325005
MGI:4358795	F	MP:0004832	enlarged ovary	Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	19325005
MGI:4358795	F	MP:0010027	increased liver cholesterol level	Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	27480224
MGI:4358795	F	MP:0005376	homeostasis/metabolism phenotype	Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	Y	27480224
MGI:4358795	F	MP:0002679	abnormal corpus luteum morphology	Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	19325005
MGI:4358795	F	MP:0004834	ovary hemorrhage	Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	19325005
MGI:4358795	F	MP:0009648	abnormal superovulation	Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	19325005
MGI:4358795	F	MP:0003507	abnormal ovary physiology	Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	19325005
MGI:4358795	M	MP:0014052	increased male germ cell apoptosis	Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17341595
MGI:4358884	M	MP:0001145	abnormal male reproductive system morphology	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17166844
MGI:4358884	M	MP:0001922	reduced male fertility	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17341595
MGI:4358884	F	MP:0008256	abnormal myometrium morphology	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17166844
MGI:4358884	M	MP:0004852	decreased testis weight	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17341595
MGI:4358884	M	MP:0003698	abnormal male reproductive system physiology	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17166844
MGI:4358884	F	MP:0001119	abnormal female reproductive system morphology	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17166844
MGI:4358884	F	MP:0002907	abnormal parturition	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17166844
MGI:4358884	M	MP:0014052	increased male germ cell apoptosis	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17341595
MGI:4358884	F	MP:0003699	abnormal female reproductive system physiology	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17166844
MGI:4358884	M	MP:0001154	seminiferous tubule degeneration	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17341595
MGI:4358884	F	MP:0009671	abnormal uterus physiology	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17166844
MGI:4358884	M	MP:0013598	Leydig cell hypertrophy	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17341595
MGI:4358884	M	MP:0002216	abnormal seminiferous tubule morphology	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17341595
MGI:4358884	M	MP:0003205	testicular atrophy	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17341595
MGI:4358884	M	MP:0002685	abnormal spermatogonia proliferation	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17341595
MGI:4358884	M	MP:0002784	abnormal Sertoli cell morphology	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>,Nr1h3<tm1Djm>/Nr1h3<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17341595
MGI:4358954	F	MP:0002907	abnormal parturition	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17166844
MGI:4358954	M	MP:0002784	abnormal Sertoli cell morphology	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17341595
MGI:4358954	M	MP:0002685	abnormal spermatogonia proliferation	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17341595
MGI:4358954	F	MP:0008256	abnormal myometrium morphology	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17166844
MGI:4358954	F	MP:0009671	abnormal uterus physiology	Nr1h2<tm1Djm>/Nr1h2<tm1Djm>	involves: 129S6/SvEvTac * C57BL/6	N	17166844
MGI:4359161	M	MP:0001262	decreased body weight	Hdac4<Gt(OST361114)Lex>/Hdac4<Gt(OST361114)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	19672313
MGI:4359195	F	MP:0000733	abnormal muscle development	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:4359195	F	MP:0002953	thick ventricular wall	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:4359195	F	MP:0010090	increased circulating creatine kinase level	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	2967442
MGI:4359195	F	MP:0010090	increased circulating creatine kinase level	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	8064326
MGI:4359195	F	MP:0009403	increased variability of skeletal muscle fiber size	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	6583703
MGI:4359195	F	MP:0003061	decreased aerobic running capacity	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	20304955
MGI:4359195	F	MP:0010090	increased circulating creatine kinase level	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	6583703
MGI:4359195	F	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	2967442
MGI:4359195	F	MP:0009414	skeletal muscle fiber necrosis	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	2967442
MGI:4359195	F	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:4359195	F	MP:0006085	myocardium necrosis	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	2967442
MGI:4359195	F	MP:0002108	abnormal muscle morphology	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	6583703
MGI:4359195	F	MP:0003105	abnormal heart atrium morphology	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:4359195	F	MP:0031131	myocardial fiber disarray	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:4359195	F	MP:0005375	adipose tissue phenotype	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	Y	20304955
MGI:4359195	F	MP:0002280	abnormal intercostal muscle morphology	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:4359195	F	MP:0009419	skeletal muscle fibrosis	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	6583703
MGI:4359195	F	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	2967442
MGI:4359195	F	MP:0008327	abnormal corticotroph morphology	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	8064326
MGI:4359195	F	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	6583703
MGI:4359195	F	MP:0005369	muscle phenotype	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	Y	20304955
MGI:4359195	F	MP:0010226	increased quadriceps weight	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	20304955
MGI:4359195	F	MP:0003852	skeletal muscle necrosis	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	6583703
MGI:4359195	F	MP:0004089	dilated sarcoplasmic reticulum	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	6583703
MGI:4359195	F	MP:0030957	abnormal myotube morphology	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:4359195	F	MP:0000752	dystrophic muscle	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	6583703
MGI:4359195	F	MP:0009405	increased skeletal muscle fiber number	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	20304955
MGI:4359195	F	MP:0002269	muscular atrophy	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	6583703
MGI:4359195	F	MP:0001923	reduced female fertility	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	6583703
MGI:4359195	F	MP:0005376	homeostasis/metabolism phenotype	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	Y	8064326
MGI:4359195	F	MP:0005376	homeostasis/metabolism phenotype	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	Y	2967442
MGI:4359195	F	MP:0000751	myopathy	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	6583703
MGI:4359195	F	MP:0010238	increased skeletal muscle weight	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	20304955
MGI:4359195	F	MP:0005137	increased growth hormone level	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	8064326
MGI:4359195	F	MP:0008416	increased somatotroph cell size	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	8064326
MGI:4359195	F	MP:0004818	increased skeletal muscle mass	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	20304955
MGI:4359195	F	MP:0000749	muscle degeneration	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	6583703
MGI:4359195	F	MP:0010106	abnormal circulating pyruvate kinase level	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	6583703
MGI:4359195	F	MP:0010581	abnormal atrium myocardial trabeculae morphology	Dmd<mdx>/Dmd<mdx>	C57BL/10ScSn-Dmd<mdx>	N	19535499
MGI:4359205	M	MP:0002741	small olfactory bulb	Arx<tm2Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359205	M	MP:0008441	thin cortical plate	Arx<tm2Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359205	M	MP:0000774	decreased brain size	Arx<tm2Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359205	M	MP:0004103	abnormal ventral striatum morphology	Arx<tm2Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359205	M	MP:0006009	abnormal neuronal migration	Arx<tm2Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359205	M	MP:0011087	neonatal lethality, complete penetrance	Arx<tm2Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359205	M	MP:0004275	abnormal postnatal subventricular zone morphology	Arx<tm2Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359206	M	MP:0001399	hyperactivity	Arx<tm3Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359206	M	MP:0009763	increased susceptibility to induced morbidity/mortality	Arx<tm3Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359206	M	MP:0001405	impaired coordination	Arx<tm3Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359206	M	MP:0003246	loss of GABAergic neurons	Arx<tm3Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359206	M	MP:0006009	abnormal neuronal migration	Arx<tm3Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359206	M	MP:0010768	mortality/aging	Arx<tm3Kki>/Y	involves: 129S/SvEv * C57BL/6J	Y	19605412
MGI:4359206	M	MP:0004000	impaired passive avoidance behavior	Arx<tm3Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359206	M	MP:0001038	abnormal cholinergic neuron morphology	Arx<tm3Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359206	M	MP:0001363	increased anxiety-related response	Arx<tm3Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359206	M	MP:0002906	increased susceptibility to pharmacologically induced seizures	Arx<tm3Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359206	M	MP:0001463	abnormal spatial learning	Arx<tm3Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359207	M	MP:0008840	abnormal spike wave discharge	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359207	M	MP:0001399	hyperactivity	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359207	M	MP:0003246	loss of GABAergic neurons	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359207	M	MP:0002826	tonic seizures	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359207	M	MP:0001363	increased anxiety-related response	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359207	M	MP:0001463	abnormal spatial learning	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359207	M	MP:0002083	premature death	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359207	M	MP:0006009	abnormal neuronal migration	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359207	M	MP:0001038	abnormal cholinergic neuron morphology	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359207	M	MP:0001405	impaired coordination	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359207	M	MP:0004000	impaired passive avoidance behavior	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359207	M	MP:0002064	seizures	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6J	N	19605412
MGI:4359380	F	MP:0001926	female infertility	Kdm1b<tm1.1Tche>/Kdm1b<tm1.1Tche>	Not Specified	N	19727073
MGI:4359634	F	MP:0001923	reduced female fertility	seb/seb	Him:OF1	N	2961926
MGI:4359634	F	MP:0004894	uterus atrophy	seb/seb	Him:OF1	N	7830374
MGI:4359634	F	MP:0001127	small ovary	seb/seb	Him:OF1	N	7830374
MGI:4359634	M	MP:0001922	reduced male fertility	seb/seb	Him:OF1	N	2961926
MGI:4359634	F	MP:0001923	reduced female fertility	seb/seb	Him:OF1	N	MGI:1889267
MGI:4359635	M	MP:0009414	skeletal muscle fiber necrosis	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	8186696
MGI:4359635	M	MP:0009420	skeletal muscle endomysial fibrosis	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	8186696
MGI:4359635	M	MP:0009461	skeletal muscle hypertrophy	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	8186696
MGI:4359635	M	MP:0002279	abnormal diaphragm morphology	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	1865908
MGI:4359635	M	MP:0002279	abnormal diaphragm morphology	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	15694130
MGI:4359635	M	MP:0002280	abnormal intercostal muscle morphology	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	1865908
MGI:4359635	M	MP:0009420	skeletal muscle endomysial fibrosis	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	17889902
MGI:4359635	M	MP:0005391	vision/eye phenotype	Dmd<mdx>/Y	involves: C57BL/10ScSn	Y	7843915
MGI:4359635	M	MP:0003631	nervous system phenotype	Dmd<mdx>/Y	involves: C57BL/10ScSn	Y	1686056
MGI:4359635	M	MP:0010254	nuclear cataract	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	2250175
MGI:4359635	M	MP:0010252	anterior subcapsular cataract	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	2250175
MGI:4359635	M	MP:0013467	diaphragmitis	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	17889902
MGI:4359635	M	MP:0004818	increased skeletal muscle mass	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	8186696
MGI:4359635	M	MP:0004510	myositis	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	17889902
MGI:4359635	M	MP:0009401	increased skeletal muscle fiber diameter	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	3209690
MGI:4359635	M	MP:0009401	increased skeletal muscle fiber diameter	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	8186696
MGI:4359635	M	MP:0004145	abnormal muscle electrophysiology	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	2250175
MGI:4359635	M	MP:0004142	abnormal muscle tone	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	3209690
MGI:4359635	M	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	8186696
MGI:4359635	M	MP:0001053	abnormal neuromuscular synapse morphology	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	1686056
MGI:4359635	M	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	3209690
MGI:4359635	M	MP:0003852	skeletal muscle necrosis	Dmd<mdx>/Y	involves: C57BL/10ScSn	N	15694130
MGI:4359806	F	MP:0001926	female infertility	st/st	Not Specified	N	16577598
MGI:4359806	M	MP:0001922	reduced male fertility	st/st	Not Specified	N	16577598
MGI:4359940	M	MP:0001922	reduced male fertility	Gpx5<tm1115.2Arte>/Gpx5<tm1115.2Arte>	involves: C57BL/6 * C57BL/6N	N	19546506
MGI:4359940	M	MP:0009232	abnormal sperm nucleus morphology	Gpx5<tm1115.2Arte>/Gpx5<tm1115.2Arte>	involves: C57BL/6 * C57BL/6N	N	19546506
MGI:4360073	F	MP:0009211	absent external female genitalia	Dact1<tm1.1Bnrc>/Dact1<tm1.1Bnrc>	B6.Cg-Dact1<tm1.1Bnrc>	N	19701191
MGI:4360073	F	MP:0003537	hydrometrocolpos	Dact1<tm1.1Bnrc>/Dact1<tm1.1Bnrc>	B6.Cg-Dact1<tm1.1Bnrc>	N	19701191
MGI:4360073	M	MP:0009204	absent external male genitalia	Dact1<tm1.1Bnrc>/Dact1<tm1.1Bnrc>	B6.Cg-Dact1<tm1.1Bnrc>	N	19701191
MGI:4360077	F	MP:0003126	abnormal external female genitalia morphology	Dact1<tm1.1Bnrc>/Dact1<tm1.1Bnrc>,Vangl2<Lp>/Vangl2<+>	B6.Cg-Vangl2<Lp> Dact1<tm1.1Bnrc>	N	19701191
MGI:4360077	M	MP:0009199	abnormal external male genitalia morphology	Dact1<tm1.1Bnrc>/Dact1<tm1.1Bnrc>,Vangl2<Lp>/Vangl2<+>	B6.Cg-Vangl2<Lp> Dact1<tm1.1Bnrc>	N	19701191
MGI:4360079	F	MP:0003126	abnormal external female genitalia morphology	Dact1<tm1.1Bnrc>/Dact1<tm1.1Bnrc>,Vangl2<Lp-m1Jus>/Vangl2<+>	involves: 101/Rl * 129 * C3H/Rl * C57BL/6	N	19701191
MGI:4360079	M	MP:0009199	abnormal external male genitalia morphology	Dact1<tm1.1Bnrc>/Dact1<tm1.1Bnrc>,Vangl2<Lp-m1Jus>/Vangl2<+>	involves: 101/Rl * 129 * C3H/Rl * C57BL/6	N	19701191
MGI:4360111	F	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx>/Dmd<+>	involves: C57BL/10ScSn	N	2407807
MGI:4360183	M	MP:0001147	small testis	Ehd4<tm1.1Haba>/Ehd4<tm1.1Haba>	involves: C57BL/6 * C57BL/6J * FVB/N	N	20213691
MGI:4360183	M	MP:0001153	small seminiferous tubules	Ehd4<tm1.1Haba>/Ehd4<tm1.1Haba>	involves: C57BL/6 * C57BL/6J * FVB/N	N	20213691
MGI:4360183	M	MP:0001156	abnormal spermatogenesis	Ehd4<tm1.1Haba>/Ehd4<tm1.1Haba>	involves: C57BL/6 * C57BL/6J * FVB/N	N	20213691
MGI:4360183	M	MP:0001922	reduced male fertility	Ehd4<tm1.1Haba>/Ehd4<tm1.1Haba>	involves: C57BL/6 * C57BL/6J * FVB/N	N	20213691
MGI:4360183	M	MP:0004852	decreased testis weight	Ehd4<tm1.1Haba>/Ehd4<tm1.1Haba>	involves: C57BL/6 * C57BL/6J * FVB/N	N	20213691
MGI:4360183	M	MP:0014052	increased male germ cell apoptosis	Ehd4<tm1.1Haba>/Ehd4<tm1.1Haba>	involves: C57BL/6 * C57BL/6J * FVB/N	N	20213691
MGI:4360183	M	MP:0006307	abnormal seminiferous tubule size	Ehd4<tm1.1Haba>/Ehd4<tm1.1Haba>	involves: C57BL/6 * C57BL/6J * FVB/N	N	20213691
MGI:4360183	M	MP:0001932	abnormal spermiogenesis	Ehd4<tm1.1Haba>/Ehd4<tm1.1Haba>	involves: C57BL/6 * C57BL/6J * FVB/N	N	20213691
MGI:4360183	M	MP:0002687	oligozoospermia	Ehd4<tm1.1Haba>/Ehd4<tm1.1Haba>	involves: C57BL/6 * C57BL/6J * FVB/N	N	20213691
MGI:4360183	M	MP:0006308	enlarged seminiferous tubules	Ehd4<tm1.1Haba>/Ehd4<tm1.1Haba>	involves: C57BL/6 * C57BL/6J * FVB/N	N	20213691
MGI:4360183	M	MP:0006380	abnormal spermatid morphology	Ehd4<tm1.1Haba>/Ehd4<tm1.1Haba>	involves: C57BL/6 * C57BL/6J * FVB/N	N	20213691
MGI:4360183	M	MP:0004901	decreased male germ cell number	Ehd4<tm1.1Haba>/Ehd4<tm1.1Haba>	involves: C57BL/6 * C57BL/6J * FVB/N	N	20213691
MGI:4360217	M	MP:0000220	increased monocyte cell number	X/Yaa	(NZB x B6.SB/Le-Yaa)F1	N	16493085
MGI:4360218	M	MP:0000220	increased monocyte cell number	Fcgr2b<tm1Ttk>/Fcgr2b<+>,X/Yaa	involves: 129S4/SvJae * C57BL/6 * SB/Le	N	16493085
MGI:4360264	F	MP:0003631	nervous system phenotype	Syn1<tm1Sud>/Syn1<tm1Sud>,Tg(Camk2a-HRAS*G12V)1Sva/0	involves: 129S7/SvEvBrd * 129T2/SvEmsJ * C57BL/6 * C57BL/6N	Y	16237176
MGI:4360341	M	MP:0008261	arrest of male meiosis	Brca1<tm2.1Cxd>/Brca1<tm2.1Cxd>,Trp53<tm1Brd>/Trp53<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB	N	12642502
MGI:4360341	M	MP:0006380	abnormal spermatid morphology	Brca1<tm2.1Cxd>/Brca1<tm2.1Cxd>,Trp53<tm1Brd>/Trp53<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB	N	12642502
MGI:4360341	M	MP:0001147	small testis	Brca1<tm2.1Cxd>/Brca1<tm2.1Cxd>,Trp53<tm1Brd>/Trp53<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB	N	12642502
MGI:4360341	M	MP:0005159	azoospermia	Brca1<tm2.1Cxd>/Brca1<tm2.1Cxd>,Trp53<tm1Brd>/Trp53<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB	N	12642502
MGI:4360341	M	MP:0001156	abnormal spermatogenesis	Brca1<tm2.1Cxd>/Brca1<tm2.1Cxd>,Trp53<tm1Brd>/Trp53<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB	N	12642502
MGI:4360341	M	MP:0005169	abnormal male meiosis	Brca1<tm2.1Cxd>/Brca1<tm2.1Cxd>,Trp53<tm1Brd>/Trp53<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB	N	12642502
MGI:4360341	M	MP:0014052	increased male germ cell apoptosis	Brca1<tm2.1Cxd>/Brca1<tm2.1Cxd>,Trp53<tm1Brd>/Trp53<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB	N	12642502
MGI:4360496	M	MP:0002064	seizures	Plp1<jp-4J>/Y	involves: C3H/HeJ * C57BL/6J	N	9215879
MGI:4360496	M	MP:0003354	astrocytosis	Plp1<jp-4J>/Y	involves: C3H/HeJ * C57BL/6J	N	8829919
MGI:4360496	M	MP:0000921	demyelination	Plp1<jp-4J>/Y	involves: C3H/HeJ * C57BL/6J	N	9215879
MGI:4360496	M	MP:0000745	tremors	Plp1<jp-4J>/Y	involves: C3H/HeJ * C57BL/6J	N	9215879
MGI:4360496	M	MP:0000921	demyelination	Plp1<jp-4J>/Y	involves: C3H/HeJ * C57BL/6J	N	8829919
MGI:4360496	M	MP:0009808	decreased oligodendrocyte number	Plp1<jp-4J>/Y	involves: C3H/HeJ * C57BL/6J	N	9215879
MGI:4360496	M	MP:0000952	abnormal CNS glial cell morphology	Plp1<jp-4J>/Y	involves: C3H/HeJ * C57BL/6J	N	8829919
MGI:4360496	M	MP:0011083	lethality at weaning, complete penetrance	Plp1<jp-4J>/Y	involves: C3H/HeJ * C57BL/6J	N	9215879
MGI:4360518	F	MP:0005387	immune system phenotype	Hprt1<tm2(CUX1)Anep>/Hprt1<+>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * FVB)	Y	17018605
MGI:4360519	F	MP:0010299	increased mammary gland tumor incidence	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	FVB.129P2-Hprt1<tm1(CUX1)Anep>	N	19738070
MGI:4360519	F	MP:0000662	abnormal branching of the mammary ductal tree	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	FVB.129P2-Hprt1<tm1(CUX1)Anep>	N	19738070
MGI:4360519	F	MP:0001883	increased mammary adenocarcinoma incidence	Hprt1<tm1(CUX1)Anep>/Hprt1<+>	FVB.129P2-Hprt1<tm1(CUX1)Anep>	N	19738070
MGI:4360520	F	MP:0010299	increased mammary gland tumor incidence	Hprt1<tm2(CUX1)Anep>/Hprt1<+>	FVB.129P2-Hprt1<tm2(CUX1)Anep>	N	19738070
MGI:4360520	F	MP:0005379	endocrine/exocrine gland phenotype	Hprt1<tm2(CUX1)Anep>/Hprt1<+>	FVB.129P2-Hprt1<tm2(CUX1)Anep>	Y	19738070
MGI:4360520	F	MP:0001883	increased mammary adenocarcinoma incidence	Hprt1<tm2(CUX1)Anep>/Hprt1<+>	FVB.129P2-Hprt1<tm2(CUX1)Anep>	N	19738070
MGI:4360539	F	MP:0031381	decreased secondary ovarian follicle number	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0011120	increased primordial ovarian follicle number	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0001132	absent mature ovarian follicles	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0001129	impaired ovarian folliculogenesis	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0001127	small ovary	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0031422	failure of superovulation	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0008871	abnormal ovarian follicle number	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0011129	decreased tertiary ovarian follicle number	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0001926	female infertility	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0011125	decreased primary ovarian follicle number	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0031015	abnormal granulosa cell apoptosis	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0003697	absent zona pellucida	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0009444	ovarian follicular cyst	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0001125	abnormal oocyte morphology	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360539	F	MP:0009093	oocyte degeneration	Tbpl2<tm1.1Lzt>/Tbpl2<tm1.1Lzt>	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	N	19759265
MGI:4360656	F	MP:0001923	reduced female fertility	Esr1<tm1.2Awo>/Esr1<tm1.2Awo>,Tg(Cga-cre)1Awo/0	involves: C57BL/6 * SJL	N	19439729
MGI:4360656	F	MP:0001926	female infertility	Esr1<tm1.2Awo>/Esr1<tm1.2Awo>,Tg(Cga-cre)1Awo/0	involves: C57BL/6 * SJL	N	19439729
MGI:4360656	F	MP:0001927	abnormal estrous cycle	Esr1<tm1.2Awo>/Esr1<tm1.2Awo>,Tg(Cga-cre)1Awo/0	involves: C57BL/6 * SJL	N	19439729
MGI:4360656	F	MP:0002680	decreased corpora lutea number	Esr1<tm1.2Awo>/Esr1<tm1.2Awo>,Tg(Cga-cre)1Awo/0	involves: C57BL/6 * SJL	N	19439729
MGI:4360656	F	MP:0001131	abnormal ovarian follicle morphology	Esr1<tm1.2Awo>/Esr1<tm1.2Awo>,Tg(Cga-cre)1Awo/0	involves: C57BL/6 * SJL	N	19439729
MGI:4360656	F	MP:0001134	absent corpus luteum	Esr1<tm1.2Awo>/Esr1<tm1.2Awo>,Tg(Cga-cre)1Awo/0	involves: C57BL/6 * SJL	N	19439729
MGI:4360683	M	MP:0001147	small testis	Atn1<tm1Rexu>/Atn1<tm1Rexu>	involves: C57BL/6	N	19681162
MGI:4360683	M	MP:0001922	reduced male fertility	Atn1<tm1Rexu>/Atn1<tm1Rexu>	involves: C57BL/6	N	19681162
MGI:4360683	M	MP:0002673	abnormal sperm number	Atn1<tm1Rexu>/Atn1<tm1Rexu>	involves: C57BL/6	N	19681162
MGI:4360685	M	MP:0002020	increased tumor incidence	Apc<tm2Rfo>/Apc<+>	(C57BL/6J x 129P2/OlaHsd)F1	N	19578404
MGI:4360685	M	MP:0003414	epidermal cyst	Apc<tm2Rfo>/Apc<+>	(C57BL/6J x 129P2/OlaHsd)F1	N	19578404
MGI:4360685	M	MP:0010338	increased desmoid tumor incidence	Apc<tm2Rfo>/Apc<+>	(C57BL/6J x 129P2/OlaHsd)F1	N	19578404
MGI:4360685	M	MP:0008019	increased liver tumor incidence	Apc<tm2Rfo>/Apc<+>	(C57BL/6J x 129P2/OlaHsd)F1	N	19578404
MGI:4360686	M	MP:0010279	increased gastrointestinal tumor incidence	Apc<tm2Rfo>/Apc<+>	129P2/OlaHsd-Apc<tm2Rfo>	N	19578404
MGI:4360692	F	MP:0001926	female infertility	Tg(Eno2-ATN1)14Tx/0	B6.Cg-Tg(Eno2-ATN1)14Tx	N	16407196
MGI:4360936	M	MP:0001156	abnormal spermatogenesis	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0013600	testis degeneration	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0001152	increased Leydig cell number	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0001147	small testis	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0001153	small seminiferous tubules	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0004901	decreased male germ cell number	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0006428	ectopic Sertoli cells	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0014052	increased male germ cell apoptosis	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0001154	seminiferous tubule degeneration	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0031407	increased Sertoli cell proliferation	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0006380	abnormal spermatid morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0004852	decreased testis weight	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0001925	male infertility	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0006362	abnormal male germ cell morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0002784	abnormal Sertoli cell morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360936	M	MP:0005159	azoospermia	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129/Sv * C57BL/6 * SJL	N	19071104
MGI:4360937	F	MP:0002637	small uterus	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0009096	decreased endometrial gland number	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0003700	abnormal oviduct transport	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0003355	decreased ovulation rate	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0001728	failure of embryo implantation	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0009071	short oviduct	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0004905	decreased uterus weight	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0008257	thin myometrium	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0001120	abnormal uterus morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0031420	decreased superovulation rate	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0003574	abnormal oviduct morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0001926	female infertility	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0004856	decreased ovary weight	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0009661	abnormal pregnancy	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360937	F	MP:0009089	short uterine horn	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129	N	18703631
MGI:4360985	M	MP:0001922	reduced male fertility	Is(17;In2)1Gso/0	involves: 101/Rl * C3H/Rl * C57BL/E * SEC/Rl	N	2320577
MGI:4361022	M	MP:0001922	reduced male fertility	Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129 * C57BL/6J	N	17951539
MGI:4361022	M	MP:0001147	small testis	Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129 * C57BL/6J	N	17951539
MGI:4361022	M	MP:0004852	decreased testis weight	Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129 * C57BL/6J	N	17951539
MGI:4361022	M	MP:0001155	arrest of spermatogenesis	Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129 * C57BL/6J	N	17951539
MGI:4361022	M	MP:0001157	small seminal vesicle	Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129 * C57BL/6J	N	17951539
MGI:4361022	M	MP:0002216	abnormal seminiferous tubule morphology	Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129 * C57BL/6J	N	17951539
MGI:4361022	M	MP:0008280	abnormal male germ cell apoptosis	Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129 * C57BL/6J	N	17951539
MGI:4361022	M	MP:0004901	decreased male germ cell number	Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129 * C57BL/6J	N	17951539
MGI:4361022	M	MP:0014269	decreased testes secretion	Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129 * C57BL/6J	N	17951539
MGI:4361022	M	MP:0002784	abnormal Sertoli cell morphology	Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129 * C57BL/6J	N	17951539
MGI:4361022	M	MP:0001153	small seminiferous tubules	Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129 * C57BL/6J	N	17951539
MGI:4361022	M	MP:0001925	male infertility	Adra1b<tm1Cta>/Adra1b<tm1Cta>	involves: 129 * C57BL/6J	N	17951539
MGI:4361117	M	MP:0001154	seminiferous tubule degeneration	Xpa<tm1Tnka>/Xpa<tm1Tnka>	involves: C57BL/6 * CBA	N	18790090
MGI:4361117	M	MP:0001156	abnormal spermatogenesis	Xpa<tm1Tnka>/Xpa<tm1Tnka>	involves: C57BL/6 * CBA	N	18790090
MGI:4361117	M	MP:0001146	abnormal testis morphology	Xpa<tm1Tnka>/Xpa<tm1Tnka>	involves: C57BL/6 * CBA	N	18790090
MGI:4361117	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Xpa<tm1Tnka>/Xpa<tm1Tnka>	involves: C57BL/6 * CBA	N	18790090
MGI:4361117	M	MP:0002631	abnormal epididymis morphology	Xpa<tm1Tnka>/Xpa<tm1Tnka>	involves: C57BL/6 * CBA	N	18790090
MGI:4361117	M	MP:0001922	reduced male fertility	Xpa<tm1Tnka>/Xpa<tm1Tnka>	involves: C57BL/6 * CBA	N	18790090
MGI:4361117	M	MP:0001152	increased Leydig cell number	Xpa<tm1Tnka>/Xpa<tm1Tnka>	involves: C57BL/6 * CBA	N	18790090
MGI:4361117	M	MP:0004852	decreased testis weight	Xpa<tm1Tnka>/Xpa<tm1Tnka>	involves: C57BL/6 * CBA	N	18790090
MGI:4361131	F	MP:0005166	decreased susceptibility to injury	Cxcr3<tm1Raks>/Cxcr3<tm1Raks>	B6.129P2-Cxcr3<tm1Raks>	N	19734217
MGI:4361131	F	MP:0005566	decreased blood urea nitrogen level	Cxcr3<tm1Raks>/Cxcr3<tm1Raks>	B6.129P2-Cxcr3<tm1Raks>	N	19734217
MGI:4361131	F	MP:0005554	decreased circulating creatinine level	Cxcr3<tm1Raks>/Cxcr3<tm1Raks>	B6.129P2-Cxcr3<tm1Raks>	N	19734217
MGI:4361131	F	MP:0002871	albuminuria	Cxcr3<tm1Raks>/Cxcr3<tm1Raks>	B6.129P2-Cxcr3<tm1Raks>	N	19734217
MGI:4361131	F	MP:0001859	kidney inflammation	Cxcr3<tm1Raks>/Cxcr3<tm1Raks>	B6.129P2-Cxcr3<tm1Raks>	N	19734217
MGI:4361176	F	MP:0001126	abnormal ovary morphology	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cyp17a1-icre)AJako/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	19423761
MGI:4361176	F	MP:0002016	ovary cyst	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cyp17a1-icre)AJako/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	19423761
MGI:4361176	F	MP:0004834	ovary hemorrhage	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cyp17a1-icre)AJako/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	19423761
MGI:4361176	F	MP:0009093	oocyte degeneration	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cyp17a1-icre)AJako/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	19423761
MGI:4361176	F	MP:0009011	prolonged diestrus	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cyp17a1-icre)AJako/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	19423761
MGI:4361176	F	MP:0031420	decreased superovulation rate	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cyp17a1-icre)AJako/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	19423761
MGI:4361176	F	MP:0001926	female infertility	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cyp17a1-icre)AJako/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	19423761
MGI:4361176	F	MP:0002680	decreased corpora lutea number	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cyp17a1-icre)AJako/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	19423761
MGI:4361176	F	MP:0008871	abnormal ovarian follicle number	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cyp17a1-icre)AJako/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	19423761
MGI:4361176	F	MP:0001927	abnormal estrous cycle	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cyp17a1-icre)AJako/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	19423761
MGI:4361176	F	MP:0009365	abnormal theca cell layer morphology	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cyp17a1-icre)AJako/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	19423761
MGI:4361176	F	MP:0009371	increased theca cell number	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cyp17a1-icre)AJako/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	19423761
MGI:4361177	M	MP:0001935	decreased litter size	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0001922	reduced male fertility	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0031436	decreased copulatory plug deposition	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0013899	abnormal seminal vesicle epithelium morphology	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0013904	abnormal seminal vesicle muscle layer morphology	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0005389	reproductive system phenotype	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	Y	18356274
MGI:4361177	M	MP:0008892	abnormal sperm flagellum morphology	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0002059	abnormal seminal vesicle morphology	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0002662	abnormal cauda epididymis morphology	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0001157	small seminal vesicle	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0009243	hairpin sperm flagellum	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0004910	decreased seminal vesicle weight	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0002673	abnormal sperm number	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0031435	abnormal copulatory plug biosynthesis	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0000242	impaired fertilization	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0002661	abnormal corpus epididymis morphology	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0009238	coiled sperm flagellum	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0013288	premature acrosome reaction	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361177	M	MP:0009237	kinked sperm flagellum	Ar<tm1Jdz>/Y,Tg(Pbsn-cre)20Fwan/?	involves: 129X1/SvJ * C57BL/6J * FVB/NCrl	N	18356274
MGI:4361283	F	MP:0009892	palate bone hypoplasia	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361283	F	MP:0009652	abnormal palatal rugae morphology	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361283	F	MP:0002896	abnormal bone mineralization	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361283	F	MP:0030266	small vomer bone	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361283	F	MP:0008273	abnormal intramembranous bone ossification	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361283	F	MP:0009890	cleft secondary palate	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361283	F	MP:0013264	tongue ankylosis	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361283	F	MP:0030183	persistent oronasal membrane	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361283	F	MP:0001954	respiratory distress	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361283	F	MP:0008970	choanal atresia	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361283	F	MP:0009895	decreased palatine bone horizontal plate size	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361283	F	MP:0011090	perinatal lethality, incomplete penetrance	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361283	F	MP:0008395	abnormal osteoblast differentiation	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361283	F	MP:0000098	abnormal vomer bone morphology	Tbx22<tm1.1Sta>/Tbx22<tm1.1Sta>	involves: 129 * CD-1	N	19648291
MGI:4361288	M	MP:0001925	male infertility	Hoxd13<Dyc>/Hoxd13<Dyc>	BALB/c-Hoxd13<Dyc>	N	19546318
MGI:4361288	M	MP:0006401	absent male preputial gland	Hoxd13<Dyc>/Hoxd13<Dyc>	BALB/c-Hoxd13<Dyc>	N	19546318
MGI:4361295	M	MP:0002169	no abnormal phenotype detected	Tbx22<tm1Sta>/Y	Not Specified	N	19648291
MGI:4361326	M	MP:0009895	decreased palatine bone horizontal plate size	Tbx22<tm1.1Sta>/Y	involves: 129/Sv * CD-1	N	19648291
MGI:4361326	M	MP:0009892	palate bone hypoplasia	Tbx22<tm1.1Sta>/Y	involves: 129/Sv * CD-1	N	19648291
MGI:4361326	M	MP:0000098	abnormal vomer bone morphology	Tbx22<tm1.1Sta>/Y	involves: 129/Sv * CD-1	N	19648291
MGI:4361326	M	MP:0008273	abnormal intramembranous bone ossification	Tbx22<tm1.1Sta>/Y	involves: 129/Sv * CD-1	N	19648291
MGI:4361326	M	MP:0011090	perinatal lethality, incomplete penetrance	Tbx22<tm1.1Sta>/Y	involves: 129/Sv * CD-1	N	19648291
MGI:4361326	M	MP:0009890	cleft secondary palate	Tbx22<tm1.1Sta>/Y	involves: 129/Sv * CD-1	N	19648291
MGI:4361326	M	MP:0009652	abnormal palatal rugae morphology	Tbx22<tm1.1Sta>/Y	involves: 129/Sv * CD-1	N	19648291
MGI:4361326	M	MP:0008970	choanal atresia	Tbx22<tm1.1Sta>/Y	involves: 129/Sv * CD-1	N	19648291
MGI:4361326	M	MP:0013264	tongue ankylosis	Tbx22<tm1.1Sta>/Y	involves: 129/Sv * CD-1	N	19648291
MGI:4361326	M	MP:0030183	persistent oronasal membrane	Tbx22<tm1.1Sta>/Y	involves: 129/Sv * CD-1	N	19648291
MGI:4361326	M	MP:0001954	respiratory distress	Tbx22<tm1.1Sta>/Y	involves: 129/Sv * CD-1	N	19648291
MGI:4361326	M	MP:0008395	abnormal osteoblast differentiation	Tbx22<tm1.1Sta>/Y	involves: 129/Sv * CD-1	N	19648291
MGI:4361326	M	MP:0002896	abnormal bone mineralization	Tbx22<tm1.1Sta>/Y	involves: 129/Sv * CD-1	N	19648291
MGI:4361327	F	MP:0002169	no abnormal phenotype detected	Tbx22<tm1Sta>/Tbx22<tm1Sta>	Not Specified	N	19648291
MGI:4361329	F	MP:0002637	small uterus	Esr1<tm2.1Gsc>/Esr1<tm2.1Gsc>	involves: 129P2/OlaHsd * C57BL/6	N	19574448
MGI:4361329	F	MP:0001926	female infertility	Esr1<tm2.1Gsc>/Esr1<tm2.1Gsc>	involves: 129P2/OlaHsd * C57BL/6	N	19574448
MGI:4361329	F	MP:0004834	ovary hemorrhage	Esr1<tm2.1Gsc>/Esr1<tm2.1Gsc>	involves: 129P2/OlaHsd * C57BL/6	N	19574448
MGI:4361329	F	MP:0000628	abnormal mammary gland development	Esr1<tm2.1Gsc>/Esr1<tm2.1Gsc>	involves: 129P2/OlaHsd * C57BL/6	N	19574448
MGI:4361338	M	MP:0009734	abnormal prostate gland duct morphology	Klf6<tm1Fjs>/Klf6<tm1Fjs>,Nkx3-1<tm3(cre)Mms>/Nkx3-1<+>	involves: 129/Sv * C57BL/6	N	19494112
MGI:4361338	M	MP:0001163	abnormal prostate gland anterior lobe morphology	Klf6<tm1Fjs>/Klf6<tm1Fjs>,Nkx3-1<tm3(cre)Mms>/Nkx3-1<+>	involves: 129/Sv * C57BL/6	N	19494112
MGI:4361338	M	MP:0009736	abnormal prostate gland branching morphogenesis	Klf6<tm1Fjs>/Klf6<tm1Fjs>,Nkx3-1<tm3(cre)Mms>/Nkx3-1<+>	involves: 129/Sv * C57BL/6	N	19494112
MGI:4361352	M	MP:0006380	abnormal spermatid morphology	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0001155	arrest of spermatogenesis	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0001732	postnatal growth retardation	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0008261	arrest of male meiosis	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0001153	small seminiferous tubules	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0014269	decreased testes secretion	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0006379	abnormal spermatocyte morphology	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0005389	reproductive system phenotype	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	Y	18987333
MGI:4361352	M	MP:0014052	increased male germ cell apoptosis	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0001925	male infertility	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0002773	decreased circulating luteinizing hormone level	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0002216	abnormal seminiferous tubule morphology	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0005536	decreased Leydig cell number	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0001265	decreased body size	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0020550	multinucleated giant male germ cells	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0004109	abnormal Sertoli cell development	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0013604	abnormal adult Leydig cell differentiation	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361352	M	MP:0002790	decreased circulating follicle stimulating hormone level	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	129/Sv-Sirt1<tm1Mcby>	N	18987333
MGI:4361353	M	MP:0003830	abnormal testis development	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	F	MP:0011125	decreased primary ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0031018	decreased granulosa cell proliferation	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	M	MP:0001147	small testis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	F	MP:0013400	abnormal endometrial gland development	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0005181	decreased circulating estradiol level	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0009009	absent estrous cycle	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0004905	decreased uterus weight	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0009444	ovarian follicular cyst	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	F	MP:0003507	abnormal ovary physiology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0009018	short estrus	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	M	MP:0001155	arrest of spermatogenesis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	F	MP:0001926	female infertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0001926	female infertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	F	MP:0001927	abnormal estrous cycle	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0011121	decreased primordial ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0004856	decreased ovary weight	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0031381	decreased secondary ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0001750	increased circulating follicle stimulating hormone level	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0011129	decreased tertiary ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	M	MP:0002286	cryptorchism	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	F	MP:0001129	impaired ovarian folliculogenesis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0009006	prolonged estrous cycle	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	M	MP:0002216	abnormal seminiferous tubule morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	M	MP:0009207	internal male genitalia hypoplasia	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	F	MP:0031420	decreased superovulation rate	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0001928	abnormal ovulation	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	F	MP:0008871	abnormal ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	F	MP:0008871	abnormal ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0005158	ovary hypoplasia	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0001134	absent corpus luteum	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	M	MP:0001925	male infertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	F	MP:0001120	abnormal uterus morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0005158	ovary hypoplasia	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	M	MP:0001940	testis hypoplasia	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	F	MP:0004834	ovary hemorrhage	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	F	MP:0001134	absent corpus luteum	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361353	F	MP:0009094	abnormal endometrial gland morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0008257	thin myometrium	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	F	MP:0009096	decreased endometrial gland number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	18703422
MGI:4361353	M	MP:0006418	abnormal testis cord formation	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	N	15118069
MGI:4361451	M	MP:0001147	small testis	Stc2<tm1Rred>/Stc2<tm1Rred>	involves: 129S1/Sv * 129X1/SvJ	N	18258678
MGI:4361452	M	MP:0001147	small testis	Stc1<tm1Rred>/Stc1<tm1Rred>,Stc2<tm1Rred>/Stc2<tm1Rred>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18258678
MGI:4361478	M	MP:0009305	decreased retroperitoneal fat pad weight	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0002773	decreased circulating luteinizing hormone level	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0001156	abnormal spermatogenesis	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0001380	reduced male mating frequency	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0009856	failure of ejaculation	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0001262	decreased body weight	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0004953	decreased spleen weight	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0006380	abnormal spermatid morphology	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0002687	oligozoospermia	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0005389	reproductive system phenotype	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	Y	17478551
MGI:4361478	M	MP:0014269	decreased testes secretion	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0030983	failure of copulatory plug deposition	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0002790	decreased circulating follicle stimulating hormone level	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0001265	decreased body size	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0001925	male infertility	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0005630	increased lung weight	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0002780	decreased circulating testosterone level	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361478	M	MP:0001153	small seminiferous tubules	Prkdc<scid>/Prkdc<scid>,Tgfb1<tm1Doe>/Tgfb1<tm1Doe>	involves: 129 * C3H * CF-1	N	17478551
MGI:4361529	F	MP:0000628	abnormal mammary gland development	Map3k14<aly>/Map3k14<aly>	involves: AEJ/GnRk * C57BL/6J	N	8299692
MGI:4361556	M	MP:0002566	abnormal sexual interaction	Lpin1<20884>/Lpin1<20884>,Nrcam<20884>/Nrcam<20884>	involves: C57BL/6J	N	19793967
MGI:4361556	F	MP:0001382	abnormal nursing	Lpin1<20884>/Lpin1<20884>,Nrcam<20884>/Nrcam<20884>	involves: C57BL/6J	N	19793967
MGI:4361575	F	MP:0002169	no abnormal phenotype detected	Atp7a<Mo-brJ>/Atp7a<+>,Mt1<tm1Bri>/Mt1<tm1Bri>,Mt2<tm1Bri>/Mt2<tm1Bri>,Tg(Mt1)174Bri/0	involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6 * SJL	N	8640230
MGI:4361577	M	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Atp7a<Mo-brJ>/Y,Mt1<tm1Bri>/Mt1<tm1Bri>,Mt2<tm1Bri>/Mt2<tm1Bri>	involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	N	8640230
MGI:4361577	M	MP:0011085	postnatal lethality, complete penetrance	Atp7a<Mo-brJ>/Y,Mt1<tm1Bri>/Mt1<tm1Bri>,Mt2<tm1Bri>/Mt2<tm1Bri>	involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	N	8640230
MGI:4361577	M	MP:0008943	increased sensitivity to induced cell death	Atp7a<Mo-brJ>/Y,Mt1<tm1Bri>/Mt1<tm1Bri>,Mt2<tm1Bri>/Mt2<tm1Bri>	involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	N	8640230
MGI:4361578	F	MP:0008943	increased sensitivity to induced cell death	Atp7a<Mo-brJ>/Atp7a<+>,Mt1<tm1Bri>/Mt1<tm1Bri>,Mt2<tm1Bri>/Mt2<tm1Bri>	involves: 129S7/SvEvBrd * C3H/HeJ	N	8640230
MGI:4361578	F	MP:0011092	embryonic lethality, complete penetrance	Atp7a<Mo-brJ>/Atp7a<+>,Mt1<tm1Bri>/Mt1<tm1Bri>,Mt2<tm1Bri>/Mt2<tm1Bri>	involves: 129S7/SvEvBrd * C3H/HeJ	N	8640230
MGI:4361578	F	MP:0001265	decreased body size	Atp7a<Mo-brJ>/Atp7a<+>,Mt1<tm1Bri>/Mt1<tm1Bri>,Mt2<tm1Bri>/Mt2<tm1Bri>	involves: 129S7/SvEvBrd * C3H/HeJ	N	8640230
MGI:4361578	F	MP:0005376	homeostasis/metabolism phenotype	Atp7a<Mo-brJ>/Atp7a<+>,Mt1<tm1Bri>/Mt1<tm1Bri>,Mt2<tm1Bri>/Mt2<tm1Bri>	involves: 129S7/SvEvBrd * C3H/HeJ	Y	8640230
MGI:4361579	M	MP:0002082	postnatal lethality	Atp7a<Mo-brJ>/Y	involves: C3H/HeJ * C57BL/6J	N	8640230
MGI:4361579	M	MP:0003067	decreased liver copper level	Atp7a<Mo-brJ>/Y	involves: C3H/HeJ * C57BL/6J	N	8640230
MGI:4361579	M	MP:0000745	tremors	Atp7a<Mo-brJ>/Y	involves: C3H/HeJ * C57BL/6J	N	8640230
MGI:4361579	M	MP:0010247	increased intestine copper level	Atp7a<Mo-brJ>/Y	involves: C3H/HeJ * C57BL/6J	N	8640230
MGI:4361579	M	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-brJ>/Y	involves: C3H/HeJ * C57BL/6J	N	8640230
MGI:4361579	M	MP:0000421	mottled coat	Atp7a<Mo-brJ>/Y	involves: C3H/HeJ * C57BL/6J	N	8640230
MGI:4361579	M	MP:0001406	abnormal gait	Atp7a<Mo-brJ>/Y	involves: C3H/HeJ * C57BL/6J	N	8640230
MGI:4361580	F	MP:0005376	homeostasis/metabolism phenotype	Atp7a<Mo-brJ>/Atp7a<+>	involves: C3H/HeJ * C57BL/6J	Y	8640230
MGI:4361625	M	MP:0013287	abnormal acrosome reaction	Pcsk4<tm1Mbi>/Pcsk4<tm1Mbi>	B6.129P2-Pcsk4<tm1Mbi>	N	16371590
MGI:4361625	M	MP:0013286	abnormal sperm capacitation	Pcsk4<tm1Mbi>/Pcsk4<tm1Mbi>	B6.129P2-Pcsk4<tm1Mbi>	N	16371590
MGI:4361625	M	MP:0001922	reduced male fertility	Pcsk4<tm1Mbi>/Pcsk4<tm1Mbi>	B6.129P2-Pcsk4<tm1Mbi>	N	16371590
MGI:4361625	M	MP:0004543	abnormal sperm physiology	Pcsk4<tm1Mbi>/Pcsk4<tm1Mbi>	B6.129P2-Pcsk4<tm1Mbi>	N	22357636
MGI:4361625	M	MP:0030978	impaired binding of sperm to zona pellucida	Pcsk4<tm1Mbi>/Pcsk4<tm1Mbi>	B6.129P2-Pcsk4<tm1Mbi>	N	16371590
MGI:4361625	M	MP:0031354	abnormal acrosome assembly	Pcsk4<tm1Mbi>/Pcsk4<tm1Mbi>	B6.129P2-Pcsk4<tm1Mbi>	N	22357636
MGI:4361625	M	MP:0009230	abnormal sperm head morphology	Pcsk4<tm1Mbi>/Pcsk4<tm1Mbi>	B6.129P2-Pcsk4<tm1Mbi>	N	22357636
MGI:4361625	M	MP:0031355	abnormal proacrosomal vesicle fusion	Pcsk4<tm1Mbi>/Pcsk4<tm1Mbi>	B6.129P2-Pcsk4<tm1Mbi>	N	22357636
MGI:4361626	M	MP:0001154	seminiferous tubule degeneration	Hip1<tm1Tsr>/Hip1<+>	involves: 129X1/SvJ * C57BL/6	N	11604514
MGI:4361634	F	MP:0003507	abnormal ovary physiology	Ahr<tm1Bra>/Ahr<tm1Bra>	B6.129-Ahr<tm1Bra>/J	N	10614669
MGI:4361634	F	MP:0011120	increased primordial ovarian follicle number	Ahr<tm1Bra>/Ahr<tm1Bra>	B6.129-Ahr<tm1Bra>/J	N	10614669
MGI:4361635	M	MP:0004910	decreased seminal vesicle weight	Ahr<tm1Bra>/Ahr<tm1Bra>	B6.129-Ahr<tm1Bra>	N	12151645
MGI:4361635	M	MP:0031359	decreased prostate gland anterior lobe weight	Ahr<tm1Bra>/Ahr<tm1Bra>	B6.129-Ahr<tm1Bra>	N	12151645
MGI:4361635	M	MP:0031366	decreased prostate gland dorsolateral lobe weight	Ahr<tm1Bra>/Ahr<tm1Bra>	B6.129-Ahr<tm1Bra>	N	12151645
MGI:4361636	M	MP:0010357	increased prostate gland tumor incidence	Ahr<tm1Bra>/Ahr<tm1Bra>,Tg(TRAMP)8247Ng/0	B6.Cg-Ahr<tm1Bra> Tg(TRAMP)8247Ng	N	17052998
MGI:4361637	M	MP:0010357	increased prostate gland tumor incidence	Ahr<tm1Bra>/Ahr<+>,Tg(TRAMP)8247Ng/0	B6.Cg-Ahr<tm1Bra> Tg(TRAMP)8247Ng	N	17052998
MGI:4361656	F	MP:0001923	reduced female fertility	Nr2f2<tm2.1Tsa>/Nr2f2<tm2.1Tsa>	involves: 129S7/SvEvBrd	N	17404209
MGI:4361657	F	MP:0004256	abnormal maternal decidual layer morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr2f2<tm2.1Tsa>/Nr2f2<tm2.1Tsa>	involves: 129S7/SvEvBrd	N	17404209
MGI:4361657	F	MP:0001729	impaired embryo implantation	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr2f2<tm2.1Tsa>/Nr2f2<tm2.1Tsa>	involves: 129S7/SvEvBrd	N	17404209
MGI:4361657	F	MP:0009089	short uterine horn	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr2f2<tm2.1Tsa>/Nr2f2<tm2.1Tsa>	involves: 129S7/SvEvBrd	N	17404209
MGI:4361657	F	MP:0031434	increased miscarriage rate	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr2f2<tm2.1Tsa>/Nr2f2<tm2.1Tsa>	involves: 129S7/SvEvBrd	N	17404209
MGI:4361657	F	MP:0001923	reduced female fertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr2f2<tm2.1Tsa>/Nr2f2<tm2.1Tsa>	involves: 129S7/SvEvBrd	N	17404209
MGI:4361657	F	MP:0004014	abnormal uterine environment	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr2f2<tm2.1Tsa>/Nr2f2<tm2.1Tsa>	involves: 129S7/SvEvBrd	N	17404209
MGI:4361657	F	MP:0031137	vaginal hemorrhage	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr2f2<tm2.1Tsa>/Nr2f2<tm2.1Tsa>	involves: 129S7/SvEvBrd	N	17404209
MGI:4361657	F	MP:0008256	abnormal myometrium morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Nr2f2<tm2.1Tsa>/Nr2f2<tm2.1Tsa>	involves: 129S7/SvEvBrd	N	17404209
MGI:4361679	M	MP:0004901	decreased male germ cell number	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361679	M	MP:0001932	abnormal spermiogenesis	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361679	M	MP:0002675	asthenozoospermia	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361679	M	MP:0002687	oligozoospermia	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361679	M	MP:0002685	abnormal spermatogonia proliferation	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361679	M	MP:0001925	male infertility	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361679	M	MP:0001154	seminiferous tubule degeneration	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361679	M	MP:0004852	decreased testis weight	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361679	M	MP:0001750	increased circulating follicle stimulating hormone level	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361679	M	MP:0001147	small testis	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361679	M	MP:0001156	abnormal spermatogenesis	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361679	M	MP:0031354	abnormal acrosome assembly	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361679	M	MP:0008995	early reproductive senescence	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361679	M	MP:0001152	increased Leydig cell number	Taf4b<tm1Rtj>/Taf4b<tm1Rtj>	B6.129-Taf4b<tm1Rtj>	N	15774719
MGI:4361734	M	MP:0005015	increased T cell number	Dmd<mdx>/Y,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361734	M	MP:0000334	decreased granulocyte number	Dmd<mdx>/Y,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361734	M	MP:0005018	decreased T cell number	Dmd<mdx>/Y,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361734	M	MP:0004262	abnormal physical strength	Dmd<mdx>/Y,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361734	M	MP:0000222	decreased neutrophil cell number	Dmd<mdx>/Y,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361734	M	MP:0002106	abnormal muscle physiology	Dmd<mdx>/Y,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361734	M	MP:0004973	increased regulatory T cell number	Dmd<mdx>/Y,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361735	F	MP:0004262	abnormal physical strength	Dmd<mdx>/Dmd<mdx>,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361735	F	MP:0000222	decreased neutrophil cell number	Dmd<mdx>/Dmd<mdx>,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361735	F	MP:0002106	abnormal muscle physiology	Dmd<mdx>/Dmd<mdx>,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361735	F	MP:0005018	decreased T cell number	Dmd<mdx>/Dmd<mdx>,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361735	F	MP:0005015	increased T cell number	Dmd<mdx>/Dmd<mdx>,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361735	F	MP:0000334	decreased granulocyte number	Dmd<mdx>/Dmd<mdx>,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361735	F	MP:0004973	increased regulatory T cell number	Dmd<mdx>/Dmd<mdx>,Spp1<tm1Blh>/Spp1<tm1Blh>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * C57BL/10ScSn	N	19451692
MGI:4361744	F	MP:0005389	reproductive system phenotype	Ndp<tm1Wbrg>/Ndp<tm1Wbrg>	involves: 129P2/OlaHsd * C57BL/6	Y	16093361
MGI:4361923	F	MP:0000627	abnormal mammary gland morphology	Shc1<tm9Paw>/Shc1<tm9Paw>,Tg(MMTV-Erbb2*,-cre)1Mul/0	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	18273058
MGI:4361924	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTV-PyVT)634Mul/0	involves: FVB/N	N	18273058
MGI:4361926	F	MP:0000627	abnormal mammary gland morphology	Shc1<tm7Paw>/Shc1<+>,Tg(MMTV-PyVT)634Mul/0	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	18273058
MGI:4361927	F	MP:0000627	abnormal mammary gland morphology	Shc1<tm6Paw>/Shc1<+>,Tg(MMTV-PyVT)634Mul/0	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	18273058
MGI:4361928	F	MP:0000627	abnormal mammary gland morphology	Shc1<tm5Paw>/Shc1<+>,Tg(MMTV-PyVT)634Mul/0	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	18273058
MGI:4361929	F	MP:0000627	abnormal mammary gland morphology	Shc1<tm5Paw>/Shc1<tm5Paw>,Tg(MMTV-PyVT)634Mul/0	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	18273058
MGI:4361930	F	MP:0000627	abnormal mammary gland morphology	Shc1<tm6Paw>/Shc1<tm6Paw>,Tg(MMTV-PyVT)634Mul/0	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	18273058
MGI:4361940	M	MP:0001783	decreased white adipose tissue amount	Npy2r<tm1.1Hhz>/Npy2r<tm1.1Hhz>,Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * BALB/cJ * C57BL/6	N	12861009
MGI:4361940	M	MP:0001431	abnormal eating behavior	Npy2r<tm1.1Hhz>/Npy2r<tm1.1Hhz>,Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * BALB/cJ * C57BL/6	N	12861009
MGI:4361940	M	MP:0001262	decreased body weight	Npy2r<tm1.1Hhz>/Npy2r<tm1.1Hhz>,Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * BALB/cJ * C57BL/6	N	12861009
MGI:4361940	M	MP:0002727	decreased circulating insulin level	Npy2r<tm1.1Hhz>/Npy2r<tm1.1Hhz>,Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * BALB/cJ * C57BL/6	N	12861009
MGI:4361940	M	MP:0005668	decreased circulating leptin level	Npy2r<tm1.1Hhz>/Npy2r<tm1.1Hhz>,Npy4r<tm1.1Hhz>/Npy4r<tm1.1Hhz>	involves: 129X1/SvJ * BALB/cJ * C57BL/6	N	12861009
MGI:4365280	M	MP:0004934	epididymis epithelium degeneration	Mfge8<tm1Shur>/Mfge8<tm1Shur>	B6.129-Mfge8<tm1Shur>	N	19240116
MGI:4365280	M	MP:0009824	spermatic granuloma	Mfge8<tm1Shur>/Mfge8<tm1Shur>	B6.129-Mfge8<tm1Shur>	N	19240116
MGI:4365280	M	MP:0001922	reduced male fertility	Mfge8<tm1Shur>/Mfge8<tm1Shur>	B6.129-Mfge8<tm1Shur>	N	19240116
MGI:4365280	M	MP:0002631	abnormal epididymis morphology	Mfge8<tm1Shur>/Mfge8<tm1Shur>	B6.129-Mfge8<tm1Shur>	N	19240116
MGI:4365281	M	MP:0031012	impaired sperm migration in female genital tract	Ros1<tm1Cbm>/Ros1<tm1Cbm>	involves: 129P2/OlaHsd * C57BL/6	N	10906072
MGI:4365281	M	MP:0001925	male infertility	Ros1<tm1Cbm>/Ros1<tm1Cbm>	involves: 129P2/OlaHsd * C57BL/6	N	10906072
MGI:4365281	M	MP:0002675	asthenozoospermia	Ros1<tm1Cbm>/Ros1<tm1Cbm>	involves: 129P2/OlaHsd * C57BL/6	N	10906072
MGI:4365281	M	MP:0009243	hairpin sperm flagellum	Ros1<tm1Cbm>/Ros1<tm1Cbm>	involves: 129P2/OlaHsd * C57BL/6	N	10906072
MGI:4365296	F	MP:0003179	thrombocytopenia	Was<tm1Itl>/Was<tm1Itl>	Not Specified	N	19805221
MGI:4365296	F	MP:0002619	abnormal lymphocyte morphology	Was<tm1Itl>/Was<tm1Itl>	Not Specified	N	19805221
MGI:4365296	F	MP:0005095	decreased T cell proliferation	Was<tm1Itl>/Was<tm1Itl>	Not Specified	N	19805221
MGI:4365296	F	MP:0005018	decreased T cell number	Was<tm1Itl>/Was<tm1Itl>	Not Specified	N	19805221
MGI:4365296	F	MP:0009338	increased splenocyte number	Was<tm1Itl>/Was<tm1Itl>	Not Specified	N	19805221
MGI:4365296	F	MP:0004762	increased anti-double stranded DNA antibody level	Was<tm1Itl>/Was<tm1Itl>	Not Specified	N	19805221
MGI:4365296	F	MP:0005461	abnormal dendritic cell morphology	Was<tm1Itl>/Was<tm1Itl>	Not Specified	N	19805221
MGI:4365296	F	MP:0000218	increased leukocyte cell number	Was<tm1Itl>/Was<tm1Itl>	Not Specified	N	19805221
MGI:4365296	F	MP:0000693	spleen hyperplasia	Was<tm1Itl>/Was<tm1Itl>	Not Specified	N	19805221
MGI:4365296	F	MP:0008173	increased follicular B cell number	Was<tm1Itl>/Was<tm1Itl>	Not Specified	N	19805221
MGI:4365296	F	MP:0005014	increased B cell number	Was<tm1Itl>/Was<tm1Itl>	Not Specified	N	19805221
MGI:4365296	F	MP:0002376	abnormal dendritic cell physiology	Was<tm1Itl>/Was<tm1Itl>	Not Specified	N	19805221
MGI:4365296	F	MP:0008045	decreased NK cell number	Was<tm1Itl>/Was<tm1Itl>	Not Specified	N	19805221
MGI:4365297	M	MP:0000218	increased leukocyte cell number	Was<tm1Itl>/Y	Not Specified	N	19805221
MGI:4365297	M	MP:0005018	decreased T cell number	Was<tm1Itl>/Y	Not Specified	N	19805221
MGI:4365297	M	MP:0003179	thrombocytopenia	Was<tm1Itl>/Y	Not Specified	N	19805221
MGI:4365297	M	MP:0008173	increased follicular B cell number	Was<tm1Itl>/Y	Not Specified	N	19805221
MGI:4365297	M	MP:0002376	abnormal dendritic cell physiology	Was<tm1Itl>/Y	Not Specified	N	19805221
MGI:4365297	M	MP:0005461	abnormal dendritic cell morphology	Was<tm1Itl>/Y	Not Specified	N	19805221
MGI:4365297	M	MP:0005095	decreased T cell proliferation	Was<tm1Itl>/Y	Not Specified	N	19805221
MGI:4365297	M	MP:0005014	increased B cell number	Was<tm1Itl>/Y	Not Specified	N	19805221
MGI:4365297	M	MP:0002619	abnormal lymphocyte morphology	Was<tm1Itl>/Y	Not Specified	N	19805221
MGI:4365297	M	MP:0008045	decreased NK cell number	Was<tm1Itl>/Y	Not Specified	N	19805221
MGI:4365297	M	MP:0009338	increased splenocyte number	Was<tm1Itl>/Y	Not Specified	N	19805221
MGI:4365297	M	MP:0000693	spleen hyperplasia	Was<tm1Itl>/Y	Not Specified	N	19805221
MGI:4365297	M	MP:0004762	increased anti-double stranded DNA antibody level	Was<tm1Itl>/Y	Not Specified	N	19805221
MGI:4365298	M	MP:0008173	increased follicular B cell number	Was<tm2Itl>/Y	Not Specified	N	19805221
MGI:4365298	M	MP:0002619	abnormal lymphocyte morphology	Was<tm2Itl>/Y	Not Specified	N	19805221
MGI:4365298	M	MP:0003179	thrombocytopenia	Was<tm2Itl>/Y	Not Specified	N	19805221
MGI:4365298	M	MP:0005018	decreased T cell number	Was<tm2Itl>/Y	Not Specified	N	19805221
MGI:4365298	M	MP:0009338	increased splenocyte number	Was<tm2Itl>/Y	Not Specified	N	19805221
MGI:4365298	M	MP:0005014	increased B cell number	Was<tm2Itl>/Y	Not Specified	N	19805221
MGI:4365298	M	MP:0002376	abnormal dendritic cell physiology	Was<tm2Itl>/Y	Not Specified	N	19805221
MGI:4365298	M	MP:0008045	decreased NK cell number	Was<tm2Itl>/Y	Not Specified	N	19805221
MGI:4365298	M	MP:0005461	abnormal dendritic cell morphology	Was<tm2Itl>/Y	Not Specified	N	19805221
MGI:4365298	M	MP:0004762	increased anti-double stranded DNA antibody level	Was<tm2Itl>/Y	Not Specified	N	19805221
MGI:4365298	M	MP:0005095	decreased T cell proliferation	Was<tm2Itl>/Y	Not Specified	N	19805221
MGI:4365298	M	MP:0000218	increased leukocyte cell number	Was<tm2Itl>/Y	Not Specified	N	19805221
MGI:4365299	F	MP:0005014	increased B cell number	Was<tm2Itl>/Was<tm2Itl>	Not Specified	N	19805221
MGI:4365299	F	MP:0005018	decreased T cell number	Was<tm2Itl>/Was<tm2Itl>	Not Specified	N	19805221
MGI:4365299	F	MP:0005461	abnormal dendritic cell morphology	Was<tm2Itl>/Was<tm2Itl>	Not Specified	N	19805221
MGI:4365299	F	MP:0002619	abnormal lymphocyte morphology	Was<tm2Itl>/Was<tm2Itl>	Not Specified	N	19805221
MGI:4365299	F	MP:0003179	thrombocytopenia	Was<tm2Itl>/Was<tm2Itl>	Not Specified	N	19805221
MGI:4365299	F	MP:0002376	abnormal dendritic cell physiology	Was<tm2Itl>/Was<tm2Itl>	Not Specified	N	19805221
MGI:4365299	F	MP:0005095	decreased T cell proliferation	Was<tm2Itl>/Was<tm2Itl>	Not Specified	N	19805221
MGI:4365299	F	MP:0008173	increased follicular B cell number	Was<tm2Itl>/Was<tm2Itl>	Not Specified	N	19805221
MGI:4365299	F	MP:0008045	decreased NK cell number	Was<tm2Itl>/Was<tm2Itl>	Not Specified	N	19805221
MGI:4365299	F	MP:0004762	increased anti-double stranded DNA antibody level	Was<tm2Itl>/Was<tm2Itl>	Not Specified	N	19805221
MGI:4365299	F	MP:0009338	increased splenocyte number	Was<tm2Itl>/Was<tm2Itl>	Not Specified	N	19805221
MGI:4365299	F	MP:0000218	increased leukocyte cell number	Was<tm2Itl>/Was<tm2Itl>	Not Specified	N	19805221
MGI:4365300	M	MP:0004762	increased anti-double stranded DNA antibody level	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365300	M	MP:0005014	increased B cell number	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365300	M	MP:0009338	increased splenocyte number	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365300	M	MP:0008045	decreased NK cell number	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365300	M	MP:0008173	increased follicular B cell number	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365300	M	MP:0000693	spleen hyperplasia	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365300	M	MP:0003179	thrombocytopenia	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365300	M	MP:0002619	abnormal lymphocyte morphology	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365300	M	MP:0000218	increased leukocyte cell number	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365300	M	MP:0005018	decreased T cell number	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365300	M	MP:0005095	decreased T cell proliferation	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365300	M	MP:0000220	increased monocyte cell number	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365300	M	MP:0002376	abnormal dendritic cell physiology	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365300	M	MP:0005461	abnormal dendritic cell morphology	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac	N	19805221
MGI:4365376	F	MP:0001129	impaired ovarian folliculogenesis	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	19351970
MGI:4365376	M	MP:0030980	abnormal acroplaxome morphology	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	21653892
MGI:4365376	M	MP:0001925	male infertility	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	19351970
MGI:4365376	F	MP:0003356	impaired luteinization	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	19351970
MGI:4365376	M	MP:0031354	abnormal acrosome assembly	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	21653892
MGI:4365376	M	MP:0001156	abnormal spermatogenesis	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	19351970
MGI:4365376	M	MP:0002686	globozoospermia	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	21653892
MGI:4365376	M	MP:0008839	absent acrosome	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	21653892
MGI:4365376	M	MP:0011743	abnormal Golgi apparatus morphology	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	21653892
MGI:4365376	M	MP:0031355	abnormal proacrosomal vesicle fusion	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	21653892
MGI:4365376	M	MP:0005159	azoospermia	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	19351970
MGI:4365376	M	MP:0006380	abnormal spermatid morphology	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	19351970
MGI:4365376	M	MP:0008279	arrest of spermiogenesis	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	21653892
MGI:4365376	F	MP:0002682	decreased mature ovarian follicle number	Fads2<tm1Mtna>/Fads2<tm1Mtna>	involves: 129S6/SvEvTac * C57BL/6J	N	19351970
MGI:4365445	M	MP:0006307	abnormal seminiferous tubule size	Klf4<tm1Khk>/Klf4<tm1Khk>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: C57BL/6 * SJL	N	18243172
MGI:4365445	M	MP:0002782	abnormal testes secretion	Klf4<tm1Khk>/Klf4<tm1Khk>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: C57BL/6 * SJL	N	18243172
MGI:4365445	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Klf4<tm1Khk>/Klf4<tm1Khk>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: C57BL/6 * SJL	N	18243172
MGI:4365445	M	MP:0004109	abnormal Sertoli cell development	Klf4<tm1Khk>/Klf4<tm1Khk>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: C57BL/6 * SJL	N	18243172
MGI:4365459	M	MP:0002687	oligozoospermia	Tnf<tm1Gkl>/Tnf<tm1Gkl>	B6;129S-Tnf<tm1Gkl>/J	N	18832037
MGI:4365459	M	MP:0001156	abnormal spermatogenesis	Tnf<tm1Gkl>/Tnf<tm1Gkl>	B6;129S-Tnf<tm1Gkl>/J	N	18832037
MGI:4365459	M	MP:0004182	abnormal spermiation	Tnf<tm1Gkl>/Tnf<tm1Gkl>	B6;129S-Tnf<tm1Gkl>/J	N	18832037
MGI:4365459	M	MP:0004852	decreased testis weight	Tnf<tm1Gkl>/Tnf<tm1Gkl>	B6;129S-Tnf<tm1Gkl>/J	N	18832037
MGI:4365459	M	MP:0014269	decreased testes secretion	Tnf<tm1Gkl>/Tnf<tm1Gkl>	B6;129S-Tnf<tm1Gkl>/J	N	18832037
MGI:4365459	M	MP:0004884	abnormal testis physiology	Tnf<tm1Gkl>/Tnf<tm1Gkl>	B6;129S-Tnf<tm1Gkl>/J	N	18832037
MGI:4365569	F	MP:0008749	abnormal peripheral T cell anergy	Rnf128<tm1.1Flv>/Rnf128<tm1.1Flv>	involves: 129S6/SvEvTac * C57BL/6	N	19805371
MGI:4365569	F	MP:0008566	increased interferon-gamma secretion	Rnf128<tm1.1Flv>/Rnf128<tm1.1Flv>	involves: 129S6/SvEvTac * C57BL/6	N	19805371
MGI:4365569	F	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology	Rnf128<tm1.1Flv>/Rnf128<tm1.1Flv>	involves: 129S6/SvEvTac * C57BL/6	N	19805371
MGI:4365569	F	MP:0008599	increased circulating interleukin-2 level	Rnf128<tm1.1Flv>/Rnf128<tm1.1Flv>	involves: 129S6/SvEvTac * C57BL/6	N	19805371
MGI:4365569	F	MP:0005348	increased T cell proliferation	Rnf128<tm1.1Flv>/Rnf128<tm1.1Flv>	involves: 129S6/SvEvTac * C57BL/6	N	19805371
MGI:4365570	M	MP:0008566	increased interferon-gamma secretion	Rnf128<tm1.1Flv>/Y	involves: 129S6/SvEvTac * C57BL/6	N	19805371
MGI:4365570	M	MP:0008599	increased circulating interleukin-2 level	Rnf128<tm1.1Flv>/Y	involves: 129S6/SvEvTac * C57BL/6	N	19805371
MGI:4365570	M	MP:0008749	abnormal peripheral T cell anergy	Rnf128<tm1.1Flv>/Y	involves: 129S6/SvEvTac * C57BL/6	N	19805371
MGI:4365570	M	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology	Rnf128<tm1.1Flv>/Y	involves: 129S6/SvEvTac * C57BL/6	N	19805371
MGI:4365570	M	MP:0005348	increased T cell proliferation	Rnf128<tm1.1Flv>/Y	involves: 129S6/SvEvTac * C57BL/6	N	19805371
MGI:4365571	F	MP:0008749	abnormal peripheral T cell anergy	Rnf128<tm1.1Flv>/Rnf128<tm1.1Flv>,Tg(TcraTcrb)425Cbn/0	involves: 129S6/SvEvTac * BALB/c * C57BL/6	N	19805371
MGI:4365571	F	MP:0008599	increased circulating interleukin-2 level	Rnf128<tm1.1Flv>/Rnf128<tm1.1Flv>,Tg(TcraTcrb)425Cbn/0	involves: 129S6/SvEvTac * BALB/c * C57BL/6	N	19805371
MGI:4365571	F	MP:0005095	decreased T cell proliferation	Rnf128<tm1.1Flv>/Rnf128<tm1.1Flv>,Tg(TcraTcrb)425Cbn/0	involves: 129S6/SvEvTac * BALB/c * C57BL/6	N	19805371
MGI:4365572	M	MP:0008599	increased circulating interleukin-2 level	Rnf128<tm1.1Flv>/Y,Tg(TcraTcrb)425Cbn/0	involves: 129S6/SvEvTac * BALB/c * C57BL/6	N	19805371
MGI:4365572	M	MP:0005095	decreased T cell proliferation	Rnf128<tm1.1Flv>/Y,Tg(TcraTcrb)425Cbn/0	involves: 129S6/SvEvTac * BALB/c * C57BL/6	N	19805371
MGI:4365572	M	MP:0008749	abnormal peripheral T cell anergy	Rnf128<tm1.1Flv>/Y,Tg(TcraTcrb)425Cbn/0	involves: 129S6/SvEvTac * BALB/c * C57BL/6	N	19805371
MGI:4365574	M	MP:0006380	abnormal spermatid morphology	Terc<tm1Rdp>/Terc<tm1Rdp>	involves: FVB/N	N	15893973
MGI:4365644	F	MP:0001926	female infertility	Sh3pxd2b<nee>/Sh3pxd2b<nee>	B10.Cg-H2<h4> Sh3pxd2b<nee>/GrsrJ	N	19669234
MGI:4365644	M	MP:0001925	male infertility	Sh3pxd2b<nee>/Sh3pxd2b<nee>	B10.Cg-H2<h4> Sh3pxd2b<nee>/GrsrJ	N	19669234
MGI:4365721	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Nkx3-1<tm4(cre/ERT2)Mms>/Nkx3-1<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	19741607
MGI:4365721	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Nkx3-1<tm4(cre/ERT2)Mms>/Nkx3-1<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	22836754
MGI:4365721	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Nkx3-1<tm4(cre/ERT2)Mms>/Nkx3-1<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	19741607
MGI:4365735	M	MP:0011091	prenatal lethality, complete penetrance	Atp6ap1<tm1Gjmm>/Y	chimera involves: 129P2/OlaHsd	N	11989824
MGI:4365747	M	MP:0002644	decreased circulating triglyceride level	Adip1<SM/J>/?,Capn10<tm1Chev>/Capn10<+>	(B6.129-Capn10<tm1Chev> x SM/J)F1	N	20388922
MGI:4365787	M	MP:0001932	abnormal spermiogenesis	skp/skp	CXB5/ByJ-skp/GrsrJ	N	MGI:4365783
MGI:4365832	M	MP:0001922	reduced male fertility	Cftr<tm1Unc>/Cftr<+>	involves: 129P2/OlaHsd	N	17519339
MGI:4365832	M	MP:0003666	impaired sperm capacitation	Cftr<tm1Unc>/Cftr<+>	involves: 129P2/OlaHsd	N	17519339
MGI:4365832	M	MP:0002675	asthenozoospermia	Cftr<tm1Unc>/Cftr<+>	involves: 129P2/OlaHsd	N	17519339
MGI:4365931	F	MP:0001926	female infertility	ur/ur	Not Specified	N	MGI:61327
MGI:4365931	M	MP:0001925	male infertility	ur/ur	Not Specified	N	MGI:61327
MGI:4365991	F	MP:0002757	decreased vertical activity	Gprasp1<tm1Ics>/Gprasp1<tm1Ics>	involves: 129S2/SvPas * C57BL/6J	N	19712096
MGI:4365991	F	MP:0009758	impaired behavioral response to cocaine	Gprasp1<tm1Ics>/Gprasp1<tm1Ics>	involves: 129S2/SvPas * C57BL/6J	N	19712096
MGI:4365991	F	MP:0005386	behavior/neurological phenotype	Gprasp1<tm1Ics>/Gprasp1<tm1Ics>	involves: 129S2/SvPas * C57BL/6J	Y	19712096
MGI:4365998	F	MP:0001926	female infertility	uns/uns	involves: C57BL/6J * CD-1	N	MGI:62314
MGI:4365998	M	MP:0001925	male infertility	uns/uns	involves: C57BL/6J * CD-1	N	MGI:62314
MGI:4366165	F	MP:0012008	delayed parturition	Ptgs1<tm1Unc>/Ptgs1<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	18833324
MGI:4366351	M	MP:0001148	enlarged testis	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	8033209
MGI:4366351	M	MP:0008456	abnormal retina rod cell outer segment morphology	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	25153086
MGI:4366351	M	MP:0001399	hyperactivity	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	25432536
MGI:4366351	M	MP:0001489	decreased startle reflex	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	25432536
MGI:4366351	M	MP:0012143	decreased a-wave amplitude	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	25153086
MGI:4366351	M	MP:0012144	decreased b-wave amplitude	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	25153086
MGI:4366351	M	MP:0004851	increased testis weight	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	8033209
MGI:4366351	M	MP:0001973	increased thermal nociceptive threshold	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	25432536
MGI:4366351	M	MP:0001463	abnormal spatial learning	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	8033209
MGI:4366351	M	MP:0001325	abnormal retina morphology	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	25153086
MGI:4366351	M	MP:0001415	increased exploration in new environment	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	8033209
MGI:4366351	M	MP:0009936	abnormal dendritic spine morphology	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	25432536
MGI:4366351	M	MP:0009141	increased prepulse inhibition	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	25432536
MGI:4366351	M	MP:0031391	increased locomotor activity	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	8033209
MGI:4366351	M	MP:0001362	abnormal anxiety-related response	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	25432536
MGI:4366437	F	MP:0003507	abnormal ovary physiology	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae * C57BL/6	N	9607805
MGI:4366437	F	MP:0001127	small ovary	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae * C57BL/6	N	9607805
MGI:4366437	F	MP:0005168	abnormal female meiosis	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae * C57BL/6	N	9607805
MGI:4366437	F	MP:0001931	abnormal oogenesis	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae * C57BL/6	N	9607805
MGI:4366437	F	MP:0012737	abnormal primary polar body morphology	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae * C57BL/6	N	9607805
MGI:4366437	F	MP:0009007	short estrous cycle	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae * C57BL/6	N	10534440
MGI:4366437	F	MP:0009648	abnormal superovulation	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae * C57BL/6	N	10534440
MGI:4366437	F	MP:0031420	decreased superovulation rate	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae * C57BL/6	N	9607805
MGI:4366437	F	MP:0001125	abnormal oocyte morphology	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae * C57BL/6	N	9607805
MGI:4366437	F	MP:0001923	reduced female fertility	Nos3<tm1Plh>/Nos3<tm1Plh>	involves: 129S4/SvJae * C57BL/6	N	9607805
MGI:4366442	M	MP:0001898	abnormal long-term depression	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd	N	16055059
MGI:4366442	M	MP:0001148	enlarged testis	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd	N	8844056
MGI:4366442	M	MP:0000877	abnormal Purkinje cell morphology	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd	N	16055059
MGI:4366442	M	MP:0004851	increased testis weight	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd	N	8844056
MGI:4366442	M	MP:0002807	abnormal eye blink conditioning behavior	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd	N	16055059
MGI:4366442	M	MP:0001488	increased startle reflex	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd	N	16055059
MGI:4366442	M	MP:0001463	abnormal spatial learning	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd	N	8844056
MGI:4366448	F	MP:0012009	early parturition	Cnr1<tm1Zim>/Cnr1<tm1Zim>,Ptgs1<tm1Unc>/Ptgs1<tm1Unc>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	18833324
MGI:4366522	M	MP:0005375	adipose tissue phenotype	Vegfd<tm1Hrl>/Y	involves: 129S/SvEv * Swiss	Y	19022221
MGI:4366522	M	MP:0005378	growth/size/body region phenotype	Vegfd<tm1Hrl>/Y	involves: 129S/SvEv * Swiss	Y	19022221
MGI:4366522	M	MP:0005387	immune system phenotype	Vegfd<tm1Hrl>/Y	involves: 129S/SvEv * Swiss	Y	19718705
MGI:4366522	M	MP:0011939	increased food intake	Vegfd<tm1Hrl>/Y	involves: 129S/SvEv * Swiss	N	19022221
MGI:4366522	M	MP:0005376	homeostasis/metabolism phenotype	Vegfd<tm1Hrl>/Y	involves: 129S/SvEv * Swiss	Y	19718705
MGI:4366523	M	MP:0001273	decreased metastatic potential	Vegfd<tm1Hrl>/Y	B6.129S-Vegfd<tm1Hrl>	N	19718705
MGI:4366524	M	MP:0004901	decreased male germ cell number	Gja1<tm1Kwi>/Gja1<tm1Kwi>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17591950
MGI:4366524	M	MP:0006378	abnormal spermatogonia morphology	Gja1<tm1Kwi>/Gja1<tm1Kwi>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17591950
MGI:4366524	M	MP:0001152	increased Leydig cell number	Gja1<tm1Kwi>/Gja1<tm1Kwi>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17591950
MGI:4366524	M	MP:0001153	small seminiferous tubules	Gja1<tm1Kwi>/Gja1<tm1Kwi>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17591950
MGI:4366524	M	MP:0004852	decreased testis weight	Gja1<tm1Kwi>/Gja1<tm1Kwi>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17591950
MGI:4366524	M	MP:0005159	azoospermia	Gja1<tm1Kwi>/Gja1<tm1Kwi>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17591950
MGI:4366524	M	MP:0006380	abnormal spermatid morphology	Gja1<tm1Kwi>/Gja1<tm1Kwi>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17591950
MGI:4366524	M	MP:0002776	increased Sertoli cell number	Gja1<tm1Kwi>/Gja1<tm1Kwi>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17591950
MGI:4366524	M	MP:0002784	abnormal Sertoli cell morphology	Gja1<tm1Kwi>/Gja1<tm1Kwi>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17591950
MGI:4366524	M	MP:0001925	male infertility	Gja1<tm1Kwi>/Gja1<tm1Kwi>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17591950
MGI:4366524	M	MP:0001147	small testis	Gja1<tm1Kwi>/Gja1<tm1Kwi>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17591950
MGI:4366524	M	MP:0001155	arrest of spermatogenesis	Gja1<tm1Kwi>/Gja1<tm1Kwi>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17591950
MGI:4366538	M	MP:0008892	abnormal sperm flagellum morphology	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0009236	pinhead sperm	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0030590	abnormal sperm fibrous sheath morphology	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0009839	multiflagellated sperm	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	12606345
MGI:4366538	M	MP:0009836	abnormal sperm principal piece morphology	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0006380	abnormal spermatid morphology	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0002686	globozoospermia	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0009831	abnormal sperm midpiece morphology	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0002216	abnormal seminiferous tubule morphology	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0001153	small seminiferous tubules	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0004543	abnormal sperm physiology	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	12606345
MGI:4366538	M	MP:0002687	oligozoospermia	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0009833	absent sperm mitochondrial sheath	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0009230	abnormal sperm head morphology	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0014468	disorganized sperm mitochondrial sheath	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0008279	arrest of spermiogenesis	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0002687	oligozoospermia	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	12606345
MGI:4366538	M	MP:0031356	abnormal outer dense fiber morphology	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	17301292
MGI:4366538	M	MP:0009230	abnormal sperm head morphology	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: CD-1	N	12606345
MGI:4366734	F	MP:0001923	reduced female fertility	Per1<tm1Brd>/Per1<tm1Brd>	129S7/SvEvBrd-Per1<tm1Brd> Hprt1<b-m2>	N	18367514
MGI:4366734	F	MP:0008995	early reproductive senescence	Per1<tm1Brd>/Per1<tm1Brd>	129S7/SvEvBrd-Per1<tm1Brd> Hprt1<b-m2>	N	18367514
MGI:4366734	F	MP:0001729	impaired embryo implantation	Per1<tm1Brd>/Per1<tm1Brd>	129S7/SvEvBrd-Per1<tm1Brd> Hprt1<b-m2>	N	18367514
MGI:4366734	F	MP:0001935	decreased litter size	Per1<tm1Brd>/Per1<tm1Brd>	129S7/SvEvBrd-Per1<tm1Brd> Hprt1<b-m2>	N	18367514
MGI:4366734	F	MP:0005449	abnormal food intake	Per1<tm1Brd>/Per1<tm1Brd>	129S7/SvEvBrd-Per1<tm1Brd> Hprt1<b-m2>	N	18367514
MGI:4366734	F	MP:0009661	abnormal pregnancy	Per1<tm1Brd>/Per1<tm1Brd>	129S7/SvEvBrd-Per1<tm1Brd> Hprt1<b-m2>	N	18367514
MGI:4366734	F	MP:0001432	abnormal food preference	Per1<tm1Brd>/Per1<tm1Brd>	129S7/SvEvBrd-Per1<tm1Brd> Hprt1<b-m2>	N	18367514
MGI:4366734	F	MP:0001927	abnormal estrous cycle	Per1<tm1Brd>/Per1<tm1Brd>	129S7/SvEvBrd-Per1<tm1Brd> Hprt1<b-m2>	N	18367514
MGI:4366734	F	MP:0001262	decreased body weight	Per1<tm1Brd>/Per1<tm1Brd>	129S7/SvEvBrd-Per1<tm1Brd> Hprt1<b-m2>	N	18367514
MGI:4366734	F	MP:0009009	absent estrous cycle	Per1<tm1Brd>/Per1<tm1Brd>	129S7/SvEvBrd-Per1<tm1Brd> Hprt1<b-m2>	N	18367514
MGI:4366734	F	MP:0008961	abnormal basal metabolism	Per1<tm1Brd>/Per1<tm1Brd>	129S7/SvEvBrd-Per1<tm1Brd> Hprt1<b-m2>	N	18367514
MGI:4366734	F	MP:0001259	abnormal body weight	Per1<tm1Brd>/Per1<tm1Brd>	129S7/SvEvBrd-Per1<tm1Brd> Hprt1<b-m2>	N	18367514
MGI:4366736	F	MP:0001926	female infertility	Tal/Tal	Not Specified	N	MGI:62288
MGI:4366736	M	MP:0001925	male infertility	Tal/Tal	Not Specified	N	MGI:62288
MGI:4366760	M	MP:0014052	increased male germ cell apoptosis	Pea15a<tm1Chne>/Pea15a<tm1Chne>	involves: C57BL/6	N	17504918
MGI:4366762	F	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-3Btlr>/Atp7a<Mo-3Btlr>	C57BL/6J-Atp7a<Mo-3Btlr>	N	22869751
MGI:4366762	F	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-3Btlr>/Atp7a<Mo-3Btlr>	C57BL/6J-Atp7a<Mo-3Btlr>	N	MGI:4361878
MGI:4366763	M	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-3Btlr>/Y	C57BL/6J-Atp7a<Mo-3Btlr>	N	MGI:4361878
MGI:4366763	M	MP:0005363	decreased susceptibility to prion infection	Atp7a<Mo-3Btlr>/Y	C57BL/6J-Atp7a<Mo-3Btlr>	N	22869751
MGI:4366763	M	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-3Btlr>/Y	C57BL/6J-Atp7a<Mo-3Btlr>	N	22869751
MGI:4366763	M	MP:0011215	decreased brain copper level	Atp7a<Mo-3Btlr>/Y	C57BL/6J-Atp7a<Mo-3Btlr>	N	22869751
MGI:4366781	M	MP:0000752	dystrophic muscle	Dmd<mdx>/Y,Nos1<tm1Plh>/Nos1<tm1Plh>	involves: 129S4/SvJae * C57BL/10ScSn	N	9681470
MGI:4366781	M	MP:0010106	abnormal circulating pyruvate kinase level	Dmd<mdx>/Y,Nos1<tm1Plh>/Nos1<tm1Plh>	involves: 129S4/SvJae * C57BL/10ScSn	N	9681470
MGI:4366782	F	MP:0010106	abnormal circulating pyruvate kinase level	Dmd<mdx>/Dmd<+>,Nos1<tm1Plh>/Nos1<tm1Plh>	involves: 129S4/SvJae * C57BL/10ScSn	N	9681470
MGI:4366782	F	MP:0000752	dystrophic muscle	Dmd<mdx>/Dmd<+>,Nos1<tm1Plh>/Nos1<tm1Plh>	involves: 129S4/SvJae * C57BL/10ScSn	N	9681470
MGI:4366784	M	MP:0010106	abnormal circulating pyruvate kinase level	Dmd<mdx>/Y	involves: 129S4/SvJae * C57BL/10ScSn	N	9681470
MGI:4366784	M	MP:0000752	dystrophic muscle	Dmd<mdx>/Y	involves: 129S4/SvJae * C57BL/10ScSn	N	9681470
MGI:4366785	F	MP:0010106	abnormal circulating pyruvate kinase level	Dmd<mdx>/Dmd<+>	involves: 129S4/SvJae * C57BL/10ScSn	N	9681470
MGI:4366785	F	MP:0000752	dystrophic muscle	Dmd<mdx>/Dmd<+>	involves: 129S4/SvJae * C57BL/10ScSn	N	9681470
MGI:4366849	M	MP:0001925	male infertility	Foxi1<tm1Sven>/Foxi1<tm1Sven>	involves: 129S1/Sv * 129X1/SvJ	N	16932748
MGI:4366849	M	MP:0031012	impaired sperm migration in female genital tract	Foxi1<tm1Sven>/Foxi1<tm1Sven>	involves: 129S1/Sv * 129X1/SvJ	N	16932748
MGI:4366849	M	MP:0004931	enlarged epididymis	Foxi1<tm1Sven>/Foxi1<tm1Sven>	involves: 129S1/Sv * 129X1/SvJ	N	16932748
MGI:4366849	M	MP:0009237	kinked sperm flagellum	Foxi1<tm1Sven>/Foxi1<tm1Sven>	involves: 129S1/Sv * 129X1/SvJ	N	16932748
MGI:4366849	M	MP:0002631	abnormal epididymis morphology	Foxi1<tm1Sven>/Foxi1<tm1Sven>	involves: 129S1/Sv * 129X1/SvJ	N	16932748
MGI:4366849	M	MP:0004928	increased epididymis weight	Foxi1<tm1Sven>/Foxi1<tm1Sven>	involves: 129S1/Sv * 129X1/SvJ	N	16932748
MGI:4366849	M	MP:0004543	abnormal sperm physiology	Foxi1<tm1Sven>/Foxi1<tm1Sven>	involves: 129S1/Sv * 129X1/SvJ	N	16932748
MGI:4366875	M	MP:0004852	decreased testis weight	Prdm1<tm1.1Clme>/Prdm1<tm1.1Liz>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ	N	19737919
MGI:4366875	M	MP:0005159	azoospermia	Prdm1<tm1.1Clme>/Prdm1<tm1.1Liz>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ	N	19737919
MGI:4366875	F	MP:0004805	absent oocytes	Prdm1<tm1.1Clme>/Prdm1<tm1.1Liz>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ	N	19737919
MGI:4367081	M	MP:0009838	abnormal sperm axoneme morphology	Meig1<tm1.2Zzha>/Meig1<tm1.2Zzha>	Not Specified	N	19805151
MGI:4367081	M	MP:0001925	male infertility	Meig1<tm1.2Zzha>/Meig1<tm1.2Zzha>	Not Specified	N	19805151
MGI:4367081	M	MP:0002675	asthenozoospermia	Meig1<tm1.2Zzha>/Meig1<tm1.2Zzha>	Not Specified	N	19805151
MGI:4367081	M	MP:0001155	arrest of spermatogenesis	Meig1<tm1.2Zzha>/Meig1<tm1.2Zzha>	Not Specified	N	19805151
MGI:4367081	M	MP:0009230	abnormal sperm head morphology	Meig1<tm1.2Zzha>/Meig1<tm1.2Zzha>	Not Specified	N	19805151
MGI:4367081	M	MP:0008545	absent sperm flagellum	Meig1<tm1.2Zzha>/Meig1<tm1.2Zzha>	Not Specified	N	19805151
MGI:4367081	M	MP:0005159	azoospermia	Meig1<tm1.2Zzha>/Meig1<tm1.2Zzha>	Not Specified	N	19805151
MGI:4367238	M	MP:0004910	decreased seminal vesicle weight	Vip<tm1Clw>/Vip<tm1Clw>	B6.129S-Vip<tm1Clw>	N	17592029
MGI:4367238	M	MP:0014269	decreased testes secretion	Vip<tm1Clw>/Vip<tm1Clw>	B6.129S-Vip<tm1Clw>	N	17592029
MGI:4367238	M	MP:0001154	seminiferous tubule degeneration	Vip<tm1Clw>/Vip<tm1Clw>	B6.129S-Vip<tm1Clw>	N	17592029
MGI:4367245	F	MP:0009006	prolonged estrous cycle	Nkx2-1<tm2Shk>/Nkx2-1<tm2Shk>,Tg(Syn1-cre)671Jxm/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	17182767
MGI:4367245	F	MP:0001928	abnormal ovulation	Nkx2-1<tm2Shk>/Nkx2-1<tm2Shk>,Tg(Syn1-cre)671Jxm/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	17182767
MGI:4367245	F	MP:0001923	reduced female fertility	Nkx2-1<tm2Shk>/Nkx2-1<tm2Shk>,Tg(Syn1-cre)671Jxm/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	17182767
MGI:4367245	F	MP:0008995	early reproductive senescence	Nkx2-1<tm2Shk>/Nkx2-1<tm2Shk>,Tg(Syn1-cre)671Jxm/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	17182767
MGI:4367245	F	MP:0009008	delayed estrous cycle	Nkx2-1<tm2Shk>/Nkx2-1<tm2Shk>,Tg(Syn1-cre)671Jxm/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	17182767
MGI:4367245	F	MP:0001938	delayed sexual maturation	Nkx2-1<tm2Shk>/Nkx2-1<tm2Shk>,Tg(Syn1-cre)671Jxm/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	17182767
MGI:4367251	M	MP:0003215	renal interstitial fibrosis	Umod<urehr4>/Umod<+>	C3HeB/FeJ-Umod<urehr4>	N	23748428
MGI:4367251	M	MP:0004154	renal tubular necrosis	Umod<urehr4>/Umod<+>	C3HeB/FeJ-Umod<urehr4>	N	23748428
MGI:4367348	M	MP:0009856	failure of ejaculation	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv * C57BL/6	N	12845227
MGI:4367348	M	MP:0001922	reduced male fertility	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv * C57BL/6	N	12845227
MGI:4367348	M	MP:0031629	abnormal mounting behavior	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv * C57BL/6	N	12845227
MGI:4367348	M	MP:0031628	abnormal intromission	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv * C57BL/6	N	12845227
MGI:4367348	M	MP:0002566	abnormal sexual interaction	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv * C57BL/6	N	12845227
MGI:4367348	M	MP:0001925	male infertility	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv * C57BL/6	N	12845227
MGI:4367348	M	MP:0001380	reduced male mating frequency	Cyp19a1<tm1Sih>/Cyp19a1<tm1Sih>	involves: 129S/SvEv * C57BL/6	N	12845227
MGI:4367617	M	MP:0001876	decreased inflammatory response	Parp1<tm1Zqw>/Parp1<tm1Zqw>	129S-Parp1<tm1Zqw>/J	N	15494543
MGI:4367617	M	MP:0005554	decreased circulating creatinine level	Parp1<tm1Zqw>/Parp1<tm1Zqw>	129S-Parp1<tm1Zqw>/J	N	15494543
MGI:4367617	M	MP:0005527	increased renal glomerular filtration rate	Parp1<tm1Zqw>/Parp1<tm1Zqw>	129S-Parp1<tm1Zqw>/J	N	15494543
MGI:4367617	M	MP:0011372	decreased renal tubule apoptosis	Parp1<tm1Zqw>/Parp1<tm1Zqw>	129S-Parp1<tm1Zqw>/J	N	15494543
MGI:4367617	M	MP:0004042	decreased susceptibility to kidney reperfusion injury	Parp1<tm1Zqw>/Parp1<tm1Zqw>	129S-Parp1<tm1Zqw>/J	N	15494543
MGI:4367735	F	MP:0003884	decreased macrophage cell number	Dmd<mdx>/Dmd<mdx>,Mmp9<tm1Tvu>/Mmp9<tm1Tvu>	B10.Cg-Mmp9<tm1Tvu> Dmd<mdx>	N	19401296
MGI:4367735	F	MP:0002108	abnormal muscle morphology	Dmd<mdx>/Dmd<mdx>,Mmp9<tm1Tvu>/Mmp9<tm1Tvu>	B10.Cg-Mmp9<tm1Tvu> Dmd<mdx>	N	19401296
MGI:4367735	F	MP:0031318	enhanced skeletal muscle regeneration	Dmd<mdx>/Dmd<mdx>,Mmp9<tm1Tvu>/Mmp9<tm1Tvu>	B10.Cg-Mmp9<tm1Tvu> Dmd<mdx>	N	19401296
MGI:4367736	F	MP:0003884	decreased macrophage cell number	Dmd<mdx>/Dmd<mdx>,Mmp9<tm1Tvu>/Mmp9<+>	B10.Cg-Mmp9<tm1Tvu> Dmd<mdx>	N	19401296
MGI:4367736	F	MP:0031318	enhanced skeletal muscle regeneration	Dmd<mdx>/Dmd<mdx>,Mmp9<tm1Tvu>/Mmp9<+>	B10.Cg-Mmp9<tm1Tvu> Dmd<mdx>	N	19401296
MGI:4367736	F	MP:0002106	abnormal muscle physiology	Dmd<mdx>/Dmd<mdx>,Mmp9<tm1Tvu>/Mmp9<+>	B10.Cg-Mmp9<tm1Tvu> Dmd<mdx>	N	19401296
MGI:4367736	F	MP:0002108	abnormal muscle morphology	Dmd<mdx>/Dmd<mdx>,Mmp9<tm1Tvu>/Mmp9<+>	B10.Cg-Mmp9<tm1Tvu> Dmd<mdx>	N	19401296
MGI:4367753	F	MP:0001926	female infertility	Hdlk/Hdlk	STOCK Hdlk/GrsrJ	N	MGI:4367716
MGI:4367753	M	MP:0001925	male infertility	Hdlk/Hdlk	STOCK Hdlk/GrsrJ	N	MGI:4367716
MGI:4367883	F	MP:0005290	decreased oxygen consumption	Apln<tm1Tq>/Apln<tm1Tq>	B6.129S6-Apln<tm1Tq>	N	19767528
MGI:4367883	F	MP:0012106	impaired exercise endurance	Apln<tm1Tq>/Apln<tm1Tq>	B6.129S6-Apln<tm1Tq>	N	19767528
MGI:4367883	F	MP:0005140	decreased cardiac muscle contractility	Apln<tm1Tq>/Apln<tm1Tq>	B6.129S6-Apln<tm1Tq>	N	19767528
MGI:4367883	F	MP:0004215	abnormal myocardial fiber physiology	Apln<tm1Tq>/Apln<tm1Tq>	B6.129S6-Apln<tm1Tq>	N	19767528
MGI:4367884	F	MP:0008779	abnormal maternal behavior	Aplnr<tm1.1Tq>/Aplnr<+>	C57BL/6-Aplnr<tm1.1Tq>	N	19767528
MGI:4367885	F	MP:0008779	abnormal maternal behavior	Aplnr<tm1.1Tq>/Aplnr<tm1.1Tq>	C57BL/6-Aplnr<tm1.1Tq>	N	19767528
MGI:4367886	M	MP:0005140	decreased cardiac muscle contractility	Apln<tm1Tq>/Y	B6.129S6-Apln<tm1Tq>	N	19767528
MGI:4367886	M	MP:0004215	abnormal myocardial fiber physiology	Apln<tm1Tq>/Y	B6.129S6-Apln<tm1Tq>	N	19767528
MGI:4367886	M	MP:0012106	impaired exercise endurance	Apln<tm1Tq>/Y	B6.129S6-Apln<tm1Tq>	N	19767528
MGI:4367886	M	MP:0005290	decreased oxygen consumption	Apln<tm1Tq>/Y	B6.129S6-Apln<tm1Tq>	N	19767528
MGI:4397574	M	MP:0000189	hypoglycemia	Tnks<Gt(RRC239)Byg>/Tnks<Gt(RRC239)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19651815
MGI:4397574	M	MP:0005668	decreased circulating leptin level	Tnks<Gt(RRC239)Byg>/Tnks<Gt(RRC239)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19651815
MGI:4397574	M	MP:0002575	increased circulating ketone body level	Tnks<Gt(RRC239)Byg>/Tnks<Gt(RRC239)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19651815
MGI:4397574	M	MP:0011939	increased food intake	Tnks<Gt(RRC239)Byg>/Tnks<Gt(RRC239)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19651815
MGI:4397574	M	MP:0002079	increased circulating insulin level	Tnks<Gt(RRC239)Byg>/Tnks<Gt(RRC239)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19651815
MGI:4397574	M	MP:0009289	decreased epididymal fat pad weight	Tnks<Gt(RRC239)Byg>/Tnks<Gt(RRC239)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19651815
MGI:4397574	M	MP:0005533	increased body temperature	Tnks<Gt(RRC239)Byg>/Tnks<Gt(RRC239)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19651815
MGI:4397574	M	MP:0004892	increased adiponectin level	Tnks<Gt(RRC239)Byg>/Tnks<Gt(RRC239)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19651815
MGI:4397574	M	MP:0009303	decreased renal fat pad weight	Tnks<Gt(RRC239)Byg>/Tnks<Gt(RRC239)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19651815
MGI:4397574	M	MP:0030021	increased muscle cell glucose uptake	Tnks<Gt(RRC239)Byg>/Tnks<Gt(RRC239)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19651815
MGI:4397574	M	MP:0005289	increased oxygen consumption	Tnks<Gt(RRC239)Byg>/Tnks<Gt(RRC239)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19651815
MGI:4397588	M	MP:0002687	oligozoospermia	Gtsf1<tm1Miya>/Gtsf1<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19735653
MGI:4397588	M	MP:0001147	small testis	Gtsf1<tm1Miya>/Gtsf1<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19735653
MGI:4397588	M	MP:0005578	teratozoospermia	Gtsf1<tm1Miya>/Gtsf1<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19735653
MGI:4397588	M	MP:0001925	male infertility	Gtsf1<tm1Miya>/Gtsf1<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19735653
MGI:4397588	M	MP:0014052	increased male germ cell apoptosis	Gtsf1<tm1Miya>/Gtsf1<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19735653
MGI:4397588	M	MP:0008261	arrest of male meiosis	Gtsf1<tm1Miya>/Gtsf1<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6	N	19735653
MGI:4397680	M	MP:0001156	abnormal spermatogenesis	Prss21<tm1Anta>/Prss21<tm1Anta>	involves: NIH Black Swiss	N	19571264
MGI:4397680	M	MP:0005578	teratozoospermia	Prss21<tm1Anta>/Prss21<tm1Anta>	involves: NIH Black Swiss	N	19571264
MGI:4397680	M	MP:0002687	oligozoospermia	Prss21<tm1Anta>/Prss21<tm1Anta>	involves: NIH Black Swiss	N	19571264
MGI:4397680	M	MP:0008893	detached sperm flagellum	Prss21<tm1Anta>/Prss21<tm1Anta>	involves: NIH Black Swiss	N	19571264
MGI:4397680	M	MP:0009243	hairpin sperm flagellum	Prss21<tm1Anta>/Prss21<tm1Anta>	involves: NIH Black Swiss	N	19571264
MGI:4397680	M	MP:0009238	coiled sperm flagellum	Prss21<tm1Anta>/Prss21<tm1Anta>	involves: NIH Black Swiss	N	19571264
MGI:4397680	M	MP:0008892	abnormal sperm flagellum morphology	Prss21<tm1Anta>/Prss21<tm1Anta>	involves: NIH Black Swiss	N	19571264
MGI:4397680	M	MP:0020451	decreased sperm progressive motility	Prss21<tm1Anta>/Prss21<tm1Anta>	involves: NIH Black Swiss	N	19571264
MGI:4397680	M	MP:0009230	abnormal sperm head morphology	Prss21<tm1Anta>/Prss21<tm1Anta>	involves: NIH Black Swiss	N	19571264
MGI:4397680	M	MP:0004543	abnormal sperm physiology	Prss21<tm1Anta>/Prss21<tm1Anta>	involves: NIH Black Swiss	N	19571264
MGI:4397700	M	MP:0002675	asthenozoospermia	Pldi<tm1.2Ploen>/Pldi<tm1.2Ploen>	involves: BALB/cJ * C57BL/6	N	19733073
MGI:4397700	M	MP:0004852	decreased testis weight	Pldi<tm1.2Ploen>/Pldi<tm1.2Ploen>	involves: BALB/cJ * C57BL/6	N	19733073
MGI:4398701	M	MP:0011833	abnormal cremaster muscle morphology	Esr1<tm1Ksk>/Esr1<+>	involves: 129P2/OlaHsd	N	8723431
MGI:4398701	M	MP:0001146	abnormal testis morphology	Esr1<tm1Ksk>/Esr1<+>	involves: 129P2/OlaHsd	N	8723431
MGI:4398703	M	MP:0001356	increased aggression towards female mice	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11114183
MGI:4398703	M	MP:0009304	increased retroperitoneal fat pad weight	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11095962
MGI:4398703	M	MP:0005669	increased circulating leptin level	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11095962
MGI:4398703	M	MP:0001556	increased circulating HDL cholesterol level	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11095962
MGI:4398703	M	MP:0003638	abnormal response/metabolism to endogenous compounds	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	12603601
MGI:4398703	M	MP:0000172	abnormal bone marrow cell number	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	12603601
MGI:4398703	M	MP:0002566	abnormal sexual interaction	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11114183
MGI:4398703	M	MP:0010024	increased total body fat amount	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11095962
MGI:4398703	M	MP:0003862	decreased aggression towards male mice	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11114183
MGI:4398703	M	MP:0002490	abnormal immunoglobulin level	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	12603601
MGI:4398703	M	MP:0009856	failure of ejaculation	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11114183
MGI:4398703	M	MP:0004816	abnormal class switch recombination	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	12603601
MGI:4398703	F	MP:0004903	abnormal uterus weight	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11557741
MGI:4398703	M	MP:0005178	increased circulating cholesterol level	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11095962
MGI:4398703	M	MP:0005331	insulin resistance	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11095962
MGI:4398703	M	MP:0009285	increased gonadal fat pad weight	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11095962
MGI:4398703	M	MP:0002458	abnormal B cell number	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	12603601
MGI:4398703	F	MP:0004905	decreased uterus weight	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11557741
MGI:4398703	M	MP:0001261	obese	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd * C57BL/6J	N	11095962
MGI:4398731	M	MP:0004543	abnormal sperm physiology	Spam1<tm1Tba>/Spam1<tm1Tba>	Not Specified	N	19605784
MGI:4398843	F	MP:0001926	female infertility	Camk2g<tm1.1Irt>/Camk2g<tm1.1Irt>	involves: C57BL/6 * C57BL/6J	N	19741297
MGI:4399118	M	MP:0009866	abnormal aorta wall morphology	Timp3<tm1Osya>/Timp3<tm1Osya>	B6.129P2-Timp3<tm1Osya>	N	23144462
MGI:4399118	M	MP:0010659	abdominal aorta aneurysm	Timp3<tm1Osya>/Timp3<tm1Osya>	B6.129P2-Timp3<tm1Osya>	N	23144462
MGI:4399118	M	MP:0000272	abnormal aorta morphology	Timp3<tm1Osya>/Timp3<tm1Osya>	B6.129P2-Timp3<tm1Osya>	N	23144462
MGI:4399118	M	MP:0002083	premature death	Timp3<tm1Osya>/Timp3<tm1Osya>	B6.129P2-Timp3<tm1Osya>	N	23144462
MGI:4399118	M	MP:0000249	abnormal blood vessel physiology	Timp3<tm1Osya>/Timp3<tm1Osya>	B6.129P2-Timp3<tm1Osya>	N	23144462
MGI:4399118	M	MP:0009870	abnormal abdominal aorta morphology	Timp3<tm1Osya>/Timp3<tm1Osya>	B6.129P2-Timp3<tm1Osya>	N	23144462
MGI:4399118	M	MP:0010139	aortitis	Timp3<tm1Osya>/Timp3<tm1Osya>	B6.129P2-Timp3<tm1Osya>	N	23144462
MGI:4410303	M	MP:0000642	enlarged adrenal glands	Tg(CAG-CYP27A1)23Etl/0	involves: C57BL/6JOlaHsd * CBA	N	12119285
MGI:4410303	F	MP:0004774	abnormal bile salt level	Tg(CAG-CYP27A1)23Etl/0	involves: C57BL/6JOlaHsd * CBA	N	12119285
MGI:4410441	M	MP:0001925	male infertility	Tg(Prm1-cre)1Mrc/0	involves: C57BL/6	N	11087830
MGI:4410618	F	MP:0003582	abnormal ovary development	Mks1<krc>/Mks1<krc>	involves: C3HeB/FeJ * C57BL/6 * CD-1	N	19776033
MGI:4411919	F	MP:0009221	uterus adenomyosis	Kras<tm4Tyj>/Kras<+>,Tg(MUC1)79.24Gend/0	involves: 129S4/SvJae * C57BL/6	N	19841240
MGI:4412038	F	MP:0001926	female infertility	smc/smc	Not Specified	N	MGI:62008
MGI:4412071	F	MP:0008720	impaired neutrophil chemotaxis	Mpp1<tm1Ahc>/Mpp1<tm1Ahc>	B6.129-Mpp1<tm1Ahc>	N	19897731
MGI:4412071	F	MP:0001935	decreased litter size	Mpp1<tm1Ahc>/Mpp1<tm1Ahc>	B6.129-Mpp1<tm1Ahc>	N	19897731
MGI:4412071	F	MP:0002463	abnormal neutrophil physiology	Mpp1<tm1Ahc>/Mpp1<tm1Ahc>	B6.129-Mpp1<tm1Ahc>	N	19897731
MGI:4412193	F	MP:0002792	abnormal retina vasculature morphology	Ndp<tm2Nat>/Ndp<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	19837032
MGI:4412193	F	MP:0004950	abnormal brain vasculature morphology	Ndp<tm2Nat>/Ndp<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	19837032
MGI:4412368	M	MP:0009243	hairpin sperm flagellum	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0002675	asthenozoospermia	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0009230	abnormal sperm head morphology	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0014052	increased male germ cell apoptosis	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0001147	small testis	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0004231	abnormal calcium ion homeostasis	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	F	MP:0005389	reproductive system phenotype	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	Y	30412589
MGI:4412368	M	MP:0001922	reduced male fertility	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0009831	abnormal sperm midpiece morphology	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0000242	impaired fertilization	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0004542	impaired acrosome reaction	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0009239	short sperm flagellum	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0000740	impaired smooth muscle contractility	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0001156	abnormal spermatogenesis	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0009647	decreased fertilization frequency	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0004901	decreased male germ cell number	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0005578	teratozoospermia	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0009836	abnormal sperm principal piece morphology	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4412368	M	MP:0004852	decreased testis weight	Mtmr14<tm1Ckq>/Mtmr14<tm1Ckq>	involves: 129S6/SvEvTac * C57BL/6J	N	30412589
MGI:4413583	M	MP:0005326	abnormal podocyte morphology	Wt1<tm1.1Lahe>/Wt1<+>	involves: 129S2/SvPas * C57BL/6 * FVB/NCrl * SJL	N	19797313
MGI:4413583	M	MP:0011871	podocyte hypertrophy	Wt1<tm1.1Lahe>/Wt1<+>	involves: 129S2/SvPas * C57BL/6 * FVB/NCrl * SJL	N	19797313
MGI:4414640	F	MP:0005060	accumulation of giant lysosomes in kidney/renal tubule cells	Clcn5<tm1Tjj>/Clcn5<+>,Clcn7<tm3.1Tjj>/Clcn7<tm3.1Tjj>,Tg(APOE-cre)VITew/0	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J	N	19661288
MGI:4414648	F	MP:0000255	blood vessel congestion	Ndp<tm1Lex>/Ndp<tm1Lex>	involves: 129S5/SvEvBrd	N	19837033
MGI:4414648	F	MP:0002792	abnormal retina vasculature morphology	Ndp<tm1Lex>/Ndp<tm1Lex>	involves: 129S5/SvEvBrd	N	19837033
MGI:4414648	F	MP:0003070	increased vascular permeability	Ndp<tm1Lex>/Ndp<tm1Lex>	involves: 129S5/SvEvBrd	N	19837033
MGI:4414649	M	MP:0003070	increased vascular permeability	Ndp<tm1Lex>/Y	involves: 129S5/SvEvBrd	N	19837033
MGI:4414649	M	MP:0000255	blood vessel congestion	Ndp<tm1Lex>/Y	involves: 129S5/SvEvBrd	N	19837033
MGI:4414649	M	MP:0002792	abnormal retina vasculature morphology	Ndp<tm1Lex>/Y	involves: 129S5/SvEvBrd	N	19837033
MGI:4414650	F	MP:0002792	abnormal retina vasculature morphology	Ndp<tm1Lex>/Ndp<tm1Lex>,Tspan12<tm1Wye>/Tspan12<+>	either: (involves: 129S5/SvEvBrd * C57BL/6) or (involves: 129S5/SvEvBrd * FVB/N)	N	19837033
MGI:4414651	M	MP:0002792	abnormal retina vasculature morphology	Ndp<tm1Lex>/Y,Tspan12<tm1Wye>/Tspan12<+>	either: (involves: 129S5/SvEvBrd * C57BL/6) or (involves: 129S5/SvEvBrd * FVB/N)	N	19837033
MGI:4414659	F	MP:0002945	abnormal inhibitory postsynaptic currents	Il1rapl1<tm1.1Hesk>/Il1rapl1<tm1.1Hesk>	involves: C57BL/6	N	19811529
MGI:4414659	F	MP:0002206	abnormal CNS synaptic transmission	Il1rapl1<tm1.1Hesk>/Il1rapl1<tm1.1Hesk>	involves: C57BL/6	N	19811529
MGI:4414659	F	MP:0000889	abnormal cerebellar molecular layer	Il1rapl1<tm1.1Hesk>/Il1rapl1<tm1.1Hesk>	involves: C57BL/6	N	19811529
MGI:4414659	F	MP:0003631	nervous system phenotype	Il1rapl1<tm1.1Hesk>/Il1rapl1<tm1.1Hesk>	involves: C57BL/6	Y	19811529
MGI:4414660	M	MP:0000889	abnormal cerebellar molecular layer	Il1rapl1<tm1.1Hesk>/Y	involves: C57BL/6	N	19811529
MGI:4414660	M	MP:0003631	nervous system phenotype	Il1rapl1<tm1.1Hesk>/Y	involves: C57BL/6	Y	19811529
MGI:4414660	M	MP:0002945	abnormal inhibitory postsynaptic currents	Il1rapl1<tm1.1Hesk>/Y	involves: C57BL/6	N	19811529
MGI:4414660	M	MP:0002206	abnormal CNS synaptic transmission	Il1rapl1<tm1.1Hesk>/Y	involves: C57BL/6	N	19811529
MGI:4414759	M	MP:0001360	abnormal social investigation	Myg1<tm1Mphi>/Myg1<tm1Mphi>	involves: 129S6/SvEvTac * C57BL/6	N	19818808
MGI:4414796	F	MP:0001926	female infertility	Zar1<tm1Zuk>/Zar1<tm1Zuk>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J	N	12539046
MGI:4414798	F	MP:0001882	abnormal lactation	Hr<N>/Hr<N>	involves: ORNL:STOCK A<w>/a Oca2<p>	N	6863894
MGI:4415047	M	MP:0004901	decreased male germ cell number	Cyp26b1<tm1Ptk>/Cyp26b1<tm1Ptk>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	19838304
MGI:4415047	M	MP:0005169	abnormal male meiosis	Cyp26b1<tm1Ptk>/Cyp26b1<tm1Ptk>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	19838304
MGI:4415047	M	MP:0001152	increased Leydig cell number	Cyp26b1<tm1Ptk>/Cyp26b1<tm1Ptk>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	19838304
MGI:4415047	M	MP:0002216	abnormal seminiferous tubule morphology	Cyp26b1<tm1Ptk>/Cyp26b1<tm1Ptk>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	19838304
MGI:4415047	M	MP:0001147	small testis	Cyp26b1<tm1Ptk>/Cyp26b1<tm1Ptk>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	19838304
MGI:4415047	M	MP:0001153	small seminiferous tubules	Cyp26b1<tm1Ptk>/Cyp26b1<tm1Ptk>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	19838304
MGI:4415047	M	MP:0001156	abnormal spermatogenesis	Cyp26b1<tm1Ptk>/Cyp26b1<tm1Ptk>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	19838304
MGI:4415293	M	MP:0001770	abnormal iron level	Gata1<tm1Mym>/Y	involves: 129P2/OlaHsd	N	10562540
MGI:4415303	M	MP:0006380	abnormal spermatid morphology	Ate1<tm1Avar>/Ate1<tm2.1Avar>,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129S1/Sv * C57BL/6 * CBA	N	19915679
MGI:4415303	M	MP:0003830	abnormal testis development	Ate1<tm1Avar>/Ate1<tm2.1Avar>,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129S1/Sv * C57BL/6 * CBA	N	19915679
MGI:4415303	M	MP:0001925	male infertility	Ate1<tm1Avar>/Ate1<tm2.1Avar>,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129S1/Sv * C57BL/6 * CBA	N	19915679
MGI:4415303	M	MP:0004901	decreased male germ cell number	Ate1<tm1Avar>/Ate1<tm2.1Avar>,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129S1/Sv * C57BL/6 * CBA	N	19915679
MGI:4415611	F	MP:0001386	abnormal maternal nurturing	lz/lz	involves: 101/H * C3H/HeH	N	MGI:61628
MGI:4415611	M	MP:0001925	male infertility	lz/lz	involves: 101/H * C3H/HeH	N	MGI:61628
MGI:4415611	F	MP:0001923	reduced female fertility	lz/lz	involves: 101/H * C3H/HeH	N	MGI:61628
MGI:4415690	M	MP:0009230	abnormal sperm head morphology	Tg(CAG-EGFP,RNU6-RNAi:Sly)367Psb/0	involves: C57BL/10 * CBA/Ca * MF1 * RIII	N	19918361
MGI:4415690	M	MP:0002674	abnormal sperm motility	Tg(CAG-EGFP,RNU6-RNAi:Sly)367Psb/0	involves: C57BL/10 * CBA/Ca * MF1 * RIII	N	19918361
MGI:4415690	M	MP:0003698	abnormal male reproductive system physiology	Tg(CAG-EGFP,RNU6-RNAi:Sly)367Psb/0	involves: C57BL/10 * CBA/Ca * MF1 * RIII	N	19918361
MGI:4415690	M	MP:0001922	reduced male fertility	Tg(CAG-EGFP,RNU6-RNAi:Sly)367Psb/0	involves: C57BL/10 * CBA/Ca * MF1 * RIII	N	19918361
MGI:4415690	M	MP:0002687	oligozoospermia	Tg(CAG-EGFP,RNU6-RNAi:Sly)367Psb/0	involves: C57BL/10 * CBA/Ca * MF1 * RIII	N	19918361
MGI:4415691	M	MP:0009230	abnormal sperm head morphology	X/Del(Y<RIII>)2Psb,Tg(CAG-EGFP,RNU6-RNAi:Sly)367Psb/0	involves: C57BL/10 * CBA/Ca * MF1 * RIII	N	19918361
MGI:4415693	M	MP:0009230	abnormal sperm head morphology	X/Del(Y<RIII>)2Psb	involves: RIII	N	19918361
MGI:4415695	M	MP:0009230	abnormal sperm head morphology	X/Del(Y)1Psb	Not Specified	N	19918361
MGI:4415697	M	MP:0006380	abnormal spermatid morphology	X/Del(Y<RIII>)2Psb	C57BL/10-Del(Y<RIII>)2Psb	N	7516747
MGI:4415697	M	MP:0002210	abnormal sex determination	X/Del(Y<RIII>)2Psb	C57BL/10-Del(Y<RIII>)2Psb	N	7516747
MGI:4415713	M	MP:0004851	increased testis weight	Fmr1<tm1Rbd>/Y	FVB.129-Fmr1<tm1Rbd>	N	20011099
MGI:4415714	M	MP:0001898	abnormal long-term depression	Fmr1<tm1Rbd>/Y	B6.129-Fmr1<tm1Rbd>	N	20011099
MGI:4415714	M	MP:0001415	increased exploration in new environment	Fmr1<tm1Rbd>/Y	B6.129-Fmr1<tm1Rbd>	N	20011099
MGI:4415714	M	MP:0001489	decreased startle reflex	Fmr1<tm1Rbd>/Y	B6.129-Fmr1<tm1Rbd>	N	20011099
MGI:4415714	M	MP:0001364	decreased anxiety-related response	Fmr1<tm1Rbd>/Y	B6.129-Fmr1<tm1Rbd>	N	20011099
MGI:4415714	M	MP:0031391	increased locomotor activity	Fmr1<tm1Rbd>/Y	B6.129-Fmr1<tm1Rbd>	N	20011099
MGI:4415714	M	MP:0001973	increased thermal nociceptive threshold	Fmr1<tm1Rbd>/Y	B6.129-Fmr1<tm1Rbd>	N	20011099
MGI:4415714	M	MP:0001409	increased stereotypic behavior	Fmr1<tm1Rbd>/Y	B6.129-Fmr1<tm1Rbd>	N	20011099
MGI:4415714	M	MP:0001496	audiogenic seizures	Fmr1<tm1Rbd>/Y	B6.129-Fmr1<tm1Rbd>	N	20011099
MGI:4415720	M	MP:0001922	reduced male fertility	Ate1<tm1Avar>/Ate1<tm2.1Avar>,Tg(Prnp-cre/ERT)28.8Ics/0	involves: 129S1/Sv * C57BL/6 * CBA * SJL	N	19915679
MGI:4415734	M	MP:0009199	abnormal external male genitalia morphology	Lrp6<tm1.2Cjz>/Lrp6<tm1.2Cjz>	involves: C57BL/6J * CD-1 * SJL	N	19653321
MGI:4415734	F	MP:0003126	abnormal external female genitalia morphology	Lrp6<tm1.2Cjz>/Lrp6<tm1.2Cjz>	involves: C57BL/6J * CD-1 * SJL	N	19653321
MGI:4415735	M	MP:0009199	abnormal external male genitalia morphology	Lrp6<tm1.2Cjz>/Lrp6<Gt(Ex187)Byg>	involves: 129P2/OlaHsd * C57BL/6J * CD-1 * SJL	N	19653321
MGI:4415735	F	MP:0003126	abnormal external female genitalia morphology	Lrp6<tm1.2Cjz>/Lrp6<Gt(Ex187)Byg>	involves: 129P2/OlaHsd * C57BL/6J * CD-1 * SJL	N	19653321
MGI:4415824	M	MP:0001577	anemia	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415824	M	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415824	M	MP:0002599	increased mean platelet volume	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415824	M	MP:0003179	thrombocytopenia	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415824	M	MP:0000229	abnormal megakaryocyte differentiation	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415824	M	MP:0002417	abnormal megakaryocyte morphology	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415824	M	MP:0008770	decreased survivor rate	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415824	M	MP:0008254	increased megakaryocyte cell number	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415825	F	MP:0008254	increased megakaryocyte cell number	Gata1<tm2Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415825	F	MP:0000229	abnormal megakaryocyte differentiation	Gata1<tm2Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415825	F	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm2Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415826	M	MP:0008254	increased megakaryocyte cell number	Gata1<tm2.1Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415826	M	MP:0002417	abnormal megakaryocyte morphology	Gata1<tm2.1Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415826	M	MP:0002599	increased mean platelet volume	Gata1<tm2.1Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415826	M	MP:0000229	abnormal megakaryocyte differentiation	Gata1<tm2.1Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415826	M	MP:0005397	hematopoietic system phenotype	Gata1<tm2.1Sho>/Y	involves: 129S4/SvJae * C57BL/6	Y	9233806
MGI:4415826	M	MP:0003179	thrombocytopenia	Gata1<tm2.1Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415826	M	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm2.1Sho>/Y	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415827	F	MP:0000229	abnormal megakaryocyte differentiation	Gata1<tm2.1Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415827	F	MP:0008254	increased megakaryocyte cell number	Gata1<tm2.1Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4415827	F	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm2.1Sho>/Gata1<+>	involves: 129S4/SvJae * C57BL/6	N	9233806
MGI:4417827	M	MP:0000219	increased neutrophil cell number	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0000691	enlarged spleen	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0000689	abnormal spleen morphology	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0002596	abnormal hematocrit	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0005016	decreased lymphocyte cell number	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0011101	prenatal lethality, incomplete penetrance	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0000691	enlarged spleen	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0000598	abnormal liver morphology	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0009338	increased splenocyte number	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0020039	increased bone ossification	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0002875	decreased erythrocyte cell number	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0000240	extramedullary hematopoiesis	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0002643	poikilocytosis	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0002356	abnormal spleen red pulp morphology	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0010178	increased number of Howell-Jolly bodies	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0011747	myelofibrosis	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0002083	premature death	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0011086	postnatal lethality, incomplete penetrance	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0003179	thrombocytopenia	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0003179	thrombocytopenia	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0006410	abnormal common myeloid progenitor cell morphology	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0008801	abnormal erythroid progenitor cell morphology	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0008801	abnormal erythroid progenitor cell morphology	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0006410	abnormal common myeloid progenitor cell morphology	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0002397	abnormal bone marrow morphology	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0001577	anemia	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0005097	polychromatophilia	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0000333	decreased bone marrow cell number	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0002397	abnormal bone marrow morphology	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0000208	decreased hematocrit	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0000333	decreased bone marrow cell number	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0003405	abnormal platelet shape	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0003405	abnormal platelet shape	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0002123	abnormal definitive hematopoiesis	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0003135	increased erythroid progenitor cell number	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0010868	increased bone trabecula number	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417827	M	MP:0008973	decreased erythroid progenitor cell number	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0008872	abnormal physiological response to xenobiotic	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	11342429
MGI:4417827	M	MP:0003135	increased erythroid progenitor cell number	Gata1<tm2Sho>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1	N	12149188
MGI:4417870	F	MP:0006269	abnormal mammary gland growth during pregnancy	Cav1<tm1Mls>/Cav1<tm1Mls>	B6.Cg-Cav1<tm1Mls>	N	12388746
MGI:4417870	F	MP:0001882	abnormal lactation	Cav1<tm1Mls>/Cav1<tm1Mls>	B6.Cg-Cav1<tm1Mls>	N	12388746
MGI:4417908	M	MP:0009269	decreased fat cell size	Tg(ACTA1-Il15*)11650Lsq/0	involves: C3H * C57BL/6	N	19001550
MGI:4417908	M	MP:0009424	decreased extensor digitorum longus weight	Tg(ACTA1-Il15*)11650Lsq/0	involves: C3H * C57BL/6	N	19001550
MGI:4417908	M	MP:0005668	decreased circulating leptin level	Tg(ACTA1-Il15*)11650Lsq/0	involves: C3H * C57BL/6	N	19001550
MGI:4417908	M	MP:0001262	decreased body weight	Tg(ACTA1-Il15*)11650Lsq/0	involves: C3H * C57BL/6	N	19001550
MGI:4417908	F	MP:0003960	increased lean body mass	Tg(ACTA1-Il15*)11650Lsq/0	involves: C3H * C57BL/6	N	19001550
MGI:4418208	F	MP:0001119	abnormal female reproductive system morphology	Gata5<tm1Eem>/Gata5<tm1Eem>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	19889636
MGI:4418221	F	MP:0010173	increased mammary gland epithelial cell proliferation	Brca1<tm5.1Cxd>/Brca1<tm5.1Cxd>	involves: 129S6/SvEvTac * FVB/N	N	19996295
MGI:4418221	F	MP:0010299	increased mammary gland tumor incidence	Brca1<tm5.1Cxd>/Brca1<tm5.1Cxd>	involves: 129S6/SvEvTac * FVB/N	N	19996295
MGI:4418221	F	MP:0009505	abnormal mammary gland lobule morphology	Brca1<tm5.1Cxd>/Brca1<tm5.1Cxd>	involves: 129S6/SvEvTac * FVB/N	N	19996295
MGI:4418221	F	MP:0000630	mammary gland hyperplasia	Brca1<tm5.1Cxd>/Brca1<tm5.1Cxd>	involves: 129S6/SvEvTac * FVB/N	N	19996295
MGI:4418221	F	MP:0014126	increased mammary gland apoptosis	Brca1<tm5.1Cxd>/Brca1<tm5.1Cxd>	involves: 129S6/SvEvTac * FVB/N	N	19996295
MGI:4418221	F	MP:0000628	abnormal mammary gland development	Brca1<tm5.1Cxd>/Brca1<tm5.1Cxd>	involves: 129S6/SvEvTac * FVB/N	N	19996295
MGI:4418221	F	MP:0000662	abnormal branching of the mammary ductal tree	Brca1<tm5.1Cxd>/Brca1<tm5.1Cxd>	involves: 129S6/SvEvTac * FVB/N	N	19996295
MGI:4418351	M	MP:0001156	abnormal spermatogenesis	Tg(CAG-SPTLC1*C133W)8EAmcc/0	involves: C3H * C57BL/6	N	16210380
MGI:4418351	M	MP:0002687	oligozoospermia	Tg(CAG-SPTLC1*C133W)8EAmcc/0	involves: C3H * C57BL/6	N	19923297
MGI:4418351	M	MP:0004852	decreased testis weight	Tg(CAG-SPTLC1*C133W)8EAmcc/0	involves: C3H * C57BL/6	N	19923297
MGI:4418351	M	MP:0002675	asthenozoospermia	Tg(CAG-SPTLC1*C133W)8EAmcc/0	involves: C3H * C57BL/6	N	19923297
MGI:4418361	M	MP:0030603	increased sperm number	Tg(CAG-Spltc1)6FAmcc/0	involves: C3H * C57BL/6	N	19923297
MGI:4418467	F	MP:0020890	abnormal milk sodium level	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Tg(MMTV-cre)1Mam/0	involves: 129S1/Sv * 129X1/SvJ * CD-1 * FVB	N	12620994
MGI:4418467	F	MP:0001882	abnormal lactation	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Tg(MMTV-cre)1Mam/0	involves: 129S1/Sv * 129X1/SvJ * CD-1 * FVB	N	12620994
MGI:4418467	F	MP:0004047	abnormal milk composition	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Tg(MMTV-cre)1Mam/0	involves: 129S1/Sv * 129X1/SvJ * CD-1 * FVB	N	12620994
MGI:4418467	F	MP:0000627	abnormal mammary gland morphology	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Tg(MMTV-cre)1Mam/0	involves: 129S1/Sv * 129X1/SvJ * CD-1 * FVB	N	12620994
MGI:4418467	F	MP:0009504	abnormal mammary gland epithelium morphology	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Tg(MMTV-cre)1Mam/0	involves: 129S1/Sv * 129X1/SvJ * CD-1 * FVB	N	12620994
MGI:4418467	F	MP:0009506	abnormal mammary gland alveolus morphology	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Tg(MMTV-cre)1Mam/0	involves: 129S1/Sv * 129X1/SvJ * CD-1 * FVB	N	12620994
MGI:4418482	F	MP:0001885	mammary gland duct hyperplasia	Cav1<tm1Mls>/Cav1<tm1Mls>,Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	N	15044451
MGI:4418482	F	MP:0009503	abnormal mammary gland duct morphology	Cav1<tm1Mls>/Cav1<tm1Mls>,Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	N	15044451
MGI:4418482	F	MP:0000662	abnormal branching of the mammary ductal tree	Cav1<tm1Mls>/Cav1<tm1Mls>,Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	N	15044451
MGI:4418492	M	MP:0002052	decreased tumor incidence	Cav1<tm1Mls>/Cav1<tm1Mls>,Tg(TRAMP)8247Ng/0	involves: 129/Sv * C57BL/6 * SJL	N	15802273
MGI:4418525	M	MP:0001859	kidney inflammation	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Gt(ROSA)26Sor<tm1Sor>/Gt(ROSA)26Sor<+>,Hprt1<tm1(Pck1-cre)Vhh>/Y	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	18037992
MGI:4418525	M	MP:0005076	abnormal cell differentiation	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Gt(ROSA)26Sor<tm1Sor>/Gt(ROSA)26Sor<+>,Hprt1<tm1(Pck1-cre)Vhh>/Y	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	18037992
MGI:4418525	M	MP:0003985	renal fibrosis	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Gt(ROSA)26Sor<tm1Sor>/Gt(ROSA)26Sor<+>,Hprt1<tm1(Pck1-cre)Vhh>/Y	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	18037992
MGI:4418525	M	MP:0005166	decreased susceptibility to injury	Hif1a<tm3Rsjo>/Hif1a<tm3Rsjo>,Gt(ROSA)26Sor<tm1Sor>/Gt(ROSA)26Sor<+>,Hprt1<tm1(Pck1-cre)Vhh>/Y	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	18037992
MGI:4418684	F	MP:0002682	decreased mature ovarian follicle number	Csf1<op>/Csf1<op>	B6;C3Fe a/a-Csf1<op>/J	N	8788202
MGI:4418684	F	MP:0001130	abnormal ovarian folliculogenesis	Csf1<op>/Csf1<op>	B6;C3Fe a/a-Csf1<op>/J	N	8788202
MGI:4418684	F	MP:0011129	decreased tertiary ovarian follicle number	Csf1<op>/Csf1<op>	B6;C3Fe a/a-Csf1<op>/J	N	8788202
MGI:4418684	F	MP:0001928	abnormal ovulation	Csf1<op>/Csf1<op>	B6;C3Fe a/a-Csf1<op>/J	N	8788202
MGI:4418684	F	MP:0003357	impaired granulosa cell differentiation	Csf1<op>/Csf1<op>	B6;C3Fe a/a-Csf1<op>/J	N	8788202
MGI:4418721	M	MP:0001156	abnormal spermatogenesis	nad/nad	C(D2)-nad	N	16542671
MGI:4418721	M	MP:0001925	male infertility	nad/nad	C(D2)-nad	N	16542671
MGI:4418758	F	MP:0006269	abnormal mammary gland growth during pregnancy	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd	N	12438700
MGI:4418758	F	MP:0009504	abnormal mammary gland epithelium morphology	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd	N	12438700
MGI:4418758	F	MP:0001884	mammary gland alveolar hyperplasia	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd	N	12438700
MGI:4418758	F	MP:0006270	abnormal mammary gland growth during lactation	Esr2<tm1Unc>/Esr2<tm1Unc>	involves: 129P2/OlaHsd	N	12438700
MGI:4418901	F	MP:0001126	abnormal ovary morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>,Inha<tm1Bay>/Inha<tm1Bay>	involves: 129P2/OlaHsd * 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4418901	F	MP:0008000	increased ovary tumor incidence	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>,Inha<tm1Bay>/Inha<tm1Bay>	involves: 129P2/OlaHsd * 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4418901	M	MP:0002216	abnormal seminiferous tubule morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>,Inha<tm1Bay>/Inha<tm1Bay>	involves: 129P2/OlaHsd * 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4418901	M	MP:0009257	dilated seminiferous tubule	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>,Inha<tm1Bay>/Inha<tm1Bay>	involves: 129P2/OlaHsd * 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4418901	M	MP:0006262	increased testis tumor incidence	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>,Inha<tm1Bay>/Inha<tm1Bay>	involves: 129P2/OlaHsd * 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4418901	M	MP:0004901	decreased male germ cell number	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>,Inha<tm1Bay>/Inha<tm1Bay>	involves: 129P2/OlaHsd * 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4418903	F	MP:0001126	abnormal ovary morphology	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>,Inha<tm1Bay>/Inha<+>	involves: 129P2/OlaHsd * 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4418903	F	MP:0008000	increased ovary tumor incidence	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>,Inha<tm1Bay>/Inha<+>	involves: 129P2/OlaHsd * 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4418904	M	MP:0009257	dilated seminiferous tubule	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * 129S6/SvEvTac	N	12855748
MGI:4418905	M	MP:0006262	increased testis tumor incidence	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Inha<tm1Bay>/Inha<tm1Bay>	involves: 129P2/OlaHsd * 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4418905	F	MP:0008000	increased ovary tumor incidence	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Inha<tm1Bay>/Inha<tm1Bay>	involves: 129P2/OlaHsd * 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4418906	F	MP:0008000	increased ovary tumor incidence	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4418906	M	MP:0006262	increased testis tumor incidence	Inha<tm1Bay>/Inha<tm1Bay>	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4418907	F	MP:0008000	increased ovary tumor incidence	Esr2<tm1Unc>/Esr2<tm1Unc>,Inha<tm1Bay>/Inha<tm1Bay>	involves: 129P2/OlaHsd * 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4418907	M	MP:0006262	increased testis tumor incidence	Esr2<tm1Unc>/Esr2<tm1Unc>,Inha<tm1Bay>/Inha<tm1Bay>	involves: 129P2/OlaHsd * 129S6/SvEvTac * 129S7/SvEvBrd	N	12855748
MGI:4420255	M	MP:0001925	male infertility	Lfng<tm1Rjo>/Lfng<tm1Rjo>,Tg(Lfng-LFNG)1Dihz/0	involves: 129S7/SvEvBrd * C57BL/6J * CBA	N	19956724
MGI:4420256	M	MP:0001925	male infertility	Lfng<tm1Rjo>/Lfng<tm1Rjo>,Tg(Lfng-LFNG)2Dihz/?	involves: 129S7/SvEvBrd * C57BL/6J * CBA	N	19956724
MGI:4420547	M	MP:0031359	decreased prostate gland anterior lobe weight	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * 129S2/SvPas	N	16014817
MGI:4420547	M	MP:0031366	decreased prostate gland dorsolateral lobe weight	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * 129S2/SvPas	N	16014817
MGI:4420547	M	MP:0031362	decreased prostate gland ventral lobe weight	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * 129S2/SvPas	N	16014817
MGI:4420547	M	MP:0004910	decreased seminal vesicle weight	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * 129S2/SvPas	N	16014817
MGI:4420930	F	MP:0001923	reduced female fertility	Wwtr1<tm1Benj>/Wwtr1<tm1Benj>	129S-Wwtr1<tm1Benj>/J	N	MGI:4420926
MGI:4420974	M	MP:0000659	prostate gland hyperplasia	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	14522255
MGI:4420974	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	14522255
MGI:4420974	M	MP:0001168	abnormal prostate gland epithelium morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	14522255
MGI:4420974	M	MP:0004958	enlarged prostate gland	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	14522255
MGI:4420974	M	MP:0003608	prostate gland inflammation	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	14522255
MGI:4420974	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	16489020
MGI:4420974	M	MP:0004961	increased prostate gland weight	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	17607361
MGI:4420974	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	17607361
MGI:4420974	M	MP:0003607	abnormal prostate gland physiology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	17607361
MGI:4420974	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	17607361
MGI:4420974	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	14522255
MGI:4420974	M	MP:0001158	abnormal prostate gland morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	17607361
MGI:4420974	M	MP:0001167	prostate gland epithelial hyperplasia	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	14522255
MGI:4420974	M	MP:0003607	abnormal prostate gland physiology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	14522255
MGI:4420975	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Hwu>/Pten<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	14522255
MGI:4421041	F	MP:0002169	no abnormal phenotype detected	Rr3<tm1Hgc>/Rr3<tm1Hgc>	involves: 129S6/SvEvTac * C57BL/6J	N	17803355
MGI:4421043	F	MP:0002169	no abnormal phenotype detected	Rr4<tm1Hgc>/Rr4<tm1Hgc>	involves: 129S6/SvEvTac * C57BL/6J	N	17803355
MGI:4421198	F	MP:0003537	hydrometrocolpos	Bmf<tm1Rjd>/Bmf<tm1Rjd>	B6.129S6-Bmf<tm1Rjd>	N	19841067
MGI:4421198	F	MP:0001144	vagina atresia	Bmf<tm1Rjd>/Bmf<tm1Rjd>	B6.129S6-Bmf<tm1Rjd>	N	19841067
MGI:4421201	F	MP:0001144	vagina atresia	Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>,Bmf<tm1Rjd>/Bmf<tm1Rjd>	B6.129S-Bcl2l11<tm1.1Ast> Bmf<tm1Rjd>	N	19841067
MGI:4421201	F	MP:0003537	hydrometrocolpos	Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>,Bmf<tm1Rjd>/Bmf<tm1Rjd>	B6.129S-Bcl2l11<tm1.1Ast> Bmf<tm1Rjd>	N	19841067
MGI:4421410	F	MP:0005386	behavior/neurological phenotype	Snca<tm1Nbm>/Snca<tm1Nbm>,Tg(SNCA*A30P)1Nbm/Tg(SNCA*A30P)1Nbm,Tg(SNCA*A30P)2Nbm/Tg(SNCA*A30P)2Nbm	involves: 129S6/SvEvTac * FVB/N	Y	20106867
MGI:4421410	F	MP:0006003	abnormal large intestinal transit time	Snca<tm1Nbm>/Snca<tm1Nbm>,Tg(SNCA*A30P)1Nbm/Tg(SNCA*A30P)1Nbm,Tg(SNCA*A30P)2Nbm/Tg(SNCA*A30P)2Nbm	involves: 129S6/SvEvTac * FVB/N	N	20106867
MGI:4421410	F	MP:0006001	abnormal intestinal transit time	Snca<tm1Nbm>/Snca<tm1Nbm>,Tg(SNCA*A30P)1Nbm/Tg(SNCA*A30P)1Nbm,Tg(SNCA*A30P)2Nbm/Tg(SNCA*A30P)2Nbm	involves: 129S6/SvEvTac * FVB/N	N	20106867
MGI:4421516	F	MP:0011941	increased fluid intake	Vamp8<tm1.1Hong>/Vamp8<tm1.1Hong>	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6	N	19841070
MGI:4421576	M	MP:0002566	abnormal sexual interaction	Grin1<tm1Yql>/Grin1<tm1Yql>,Tg(Ppp1r2-cre)4127Nkza/0	involves: C57BL/6N	N	19915563
MGI:4421666	M	MP:0001925	male infertility	Meig1<tm1Shpi>/Meig1<tm1Shpi>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	20004656
MGI:4421666	M	MP:0008892	abnormal sperm flagellum morphology	Meig1<tm1Shpi>/Meig1<tm1Shpi>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	20004656
MGI:4421666	M	MP:0001156	abnormal spermatogenesis	Meig1<tm1Shpi>/Meig1<tm1Shpi>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	20004656
MGI:4421666	M	MP:0005578	teratozoospermia	Meig1<tm1Shpi>/Meig1<tm1Shpi>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	20004656
MGI:4421666	M	MP:0014052	increased male germ cell apoptosis	Meig1<tm1Shpi>/Meig1<tm1Shpi>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	20004656
MGI:4421666	M	MP:0020869	immotile sperm	Meig1<tm1Shpi>/Meig1<tm1Shpi>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	20004656
MGI:4421666	M	MP:0002687	oligozoospermia	Meig1<tm1Shpi>/Meig1<tm1Shpi>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	20004656
MGI:4421666	M	MP:0009230	abnormal sperm head morphology	Meig1<tm1Shpi>/Meig1<tm1Shpi>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	20004656
MGI:4421666	M	MP:0009233	enlarged sperm head	Meig1<tm1Shpi>/Meig1<tm1Shpi>	involves: 129S1/Sv * 129X1/SvJ * BALB/c	N	20004656
MGI:4421786	M	MP:0001922	reduced male fertility	Pgk2<tm1Dao>/Pgk2<tm1Dao>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	19759366
MGI:4421786	M	MP:0005389	reproductive system phenotype	Pgk2<tm1Dao>/Pgk2<tm1Dao>	involves: 129S6/SvEvTac * C57BL/6NCrl	Y	19759366
MGI:4421786	M	MP:0002675	asthenozoospermia	Pgk2<tm1Dao>/Pgk2<tm1Dao>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	19759366
MGI:4421786	M	MP:0020451	decreased sperm progressive motility	Pgk2<tm1Dao>/Pgk2<tm1Dao>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	19759366
MGI:4421786	M	MP:0001925	male infertility	Pgk2<tm1Dao>/Pgk2<tm1Dao>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	19759366
MGI:4421789	F	MP:0001923	reduced female fertility	Om/Om<+>	either: (DDK x C57BL/6J)F1 or (DDK x KK)F1 or (DDK x NC)F1	N	4431024
MGI:4421789	F	MP:0005168	abnormal female meiosis	Om/Om<+>	either: (DDK x C57BL/6J)F1 or (DDK x KK)F1 or (DDK x NC)F1	N	15744049
MGI:4421834	M	MP:0001147	small testis	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19696012
MGI:4421834	M	MP:0001154	seminiferous tubule degeneration	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19696012
MGI:4421834	F	MP:0001926	female infertility	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21277975
MGI:4421834	M	MP:0001154	seminiferous tubule degeneration	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21277975
MGI:4421834	M	MP:0001156	abnormal spermatogenesis	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19696012
MGI:4421834	M	MP:0001925	male infertility	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19696012
MGI:4421834	F	MP:0000242	impaired fertilization	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21277975
MGI:4421834	F	MP:0005168	abnormal female meiosis	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21277975
MGI:4421834	M	MP:0001925	male infertility	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21277975
MGI:4421834	F	MP:0001931	abnormal oogenesis	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21277975
MGI:4421834	F	MP:0001926	female infertility	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19696012
MGI:4421834	M	MP:0005159	azoospermia	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19696012
MGI:4421834	M	MP:0004852	decreased testis weight	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21277975
MGI:4421834	M	MP:0006380	abnormal spermatid morphology	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19696012
MGI:4421834	M	MP:0002685	abnormal spermatogonia proliferation	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19696012
MGI:4421834	M	MP:0001156	abnormal spermatogenesis	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21277975
MGI:4421834	F	MP:0014443	impaired polar body extrusion	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21277975
MGI:4421834	M	MP:0002216	abnormal seminiferous tubule morphology	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19696012
MGI:4421834	M	MP:0008995	early reproductive senescence	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21277975
MGI:4421834	M	MP:0004901	decreased male germ cell number	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21277975
MGI:4421834	M	MP:0002631	abnormal epididymis morphology	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19696012
MGI:4421834	M	MP:0004901	decreased male germ cell number	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	19696012
MGI:4421838	M	MP:0002675	asthenozoospermia	Del(16Tssk1-Tssk2)1Agr/Del(16Tssk1-Tssk2)1Agr	B6.129S5(Cg)-Del(16Tssk1-Tssk2)1Agr	N	20053632
MGI:4421838	M	MP:0001156	abnormal spermatogenesis	Del(16Tssk1-Tssk2)1Agr/Del(16Tssk1-Tssk2)1Agr	B6.129S5(Cg)-Del(16Tssk1-Tssk2)1Agr	N	20053632
MGI:4421838	M	MP:0002687	oligozoospermia	Del(16Tssk1-Tssk2)1Agr/Del(16Tssk1-Tssk2)1Agr	B6.129S5(Cg)-Del(16Tssk1-Tssk2)1Agr	N	20053632
MGI:4421838	M	MP:0005578	teratozoospermia	Del(16Tssk1-Tssk2)1Agr/Del(16Tssk1-Tssk2)1Agr	B6.129S5(Cg)-Del(16Tssk1-Tssk2)1Agr	N	20053632
MGI:4421838	M	MP:0001925	male infertility	Del(16Tssk1-Tssk2)1Agr/Del(16Tssk1-Tssk2)1Agr	B6.129S5(Cg)-Del(16Tssk1-Tssk2)1Agr	N	20053632
MGI:4421856	F	MP:0001382	abnormal nursing	Hr<rh-R>/Hr<rh-R>	involves: 101 * C3H/Rl * C57BL/RlEl * C57BL/10Rl * SEC/El	N	20080498
MGI:4422096	F	MP:0005387	immune system phenotype	Tlr13<m1Btlr>/Tlr13<m1Btlr>	C57BL/6J-Tlr13<m1Btlr>	Y	MGI:4421550
MGI:4422098	M	MP:0004852	decreased testis weight	Tdrd9<tm1.1Chum>/Tdrd9<tm1.1Chum>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20059948
MGI:4422098	M	MP:0005159	azoospermia	Tdrd9<tm1.1Chum>/Tdrd9<tm1.1Chum>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20059948
MGI:4422098	M	MP:0006378	abnormal spermatogonia morphology	Tdrd9<tm1.1Chum>/Tdrd9<tm1.1Chum>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20059948
MGI:4422098	M	MP:0008261	arrest of male meiosis	Tdrd9<tm1.1Chum>/Tdrd9<tm1.1Chum>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20059948
MGI:4422098	M	MP:0001147	small testis	Tdrd9<tm1.1Chum>/Tdrd9<tm1.1Chum>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20059948
MGI:4422098	M	MP:0006362	abnormal male germ cell morphology	Tdrd9<tm1.1Chum>/Tdrd9<tm1.1Chum>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20059948
MGI:4422098	M	MP:0006379	abnormal spermatocyte morphology	Tdrd9<tm1.1Chum>/Tdrd9<tm1.1Chum>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20059948
MGI:4422098	M	MP:0014052	increased male germ cell apoptosis	Tdrd9<tm1.1Chum>/Tdrd9<tm1.1Chum>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20059948
MGI:4422098	M	MP:0001925	male infertility	Tdrd9<tm1.1Chum>/Tdrd9<tm1.1Chum>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20059948
MGI:4422197	F	MP:0001881	abnormal mammary gland physiology	Pgr<tm1Bwo>/Pgr<tm1Bwo>	involves: 129S7/SvEvBrd	N	20029965
MGI:4422197	F	MP:0009504	abnormal mammary gland epithelium morphology	Pgr<tm1Bwo>/Pgr<tm1Bwo>	involves: 129S7/SvEvBrd	N	14667968
MGI:4422197	F	MP:0031422	failure of superovulation	Pgr<tm1Bwo>/Pgr<tm1Bwo>	involves: 129S7/SvEvBrd	N	20029965
MGI:4422197	F	MP:0009506	abnormal mammary gland alveolus morphology	Pgr<tm1Bwo>/Pgr<tm1Bwo>	involves: 129S7/SvEvBrd	N	12897242
MGI:4422197	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Pgr<tm1Bwo>/Pgr<tm1Bwo>	involves: 129S7/SvEvBrd	N	12897242
MGI:4422197	F	MP:0009671	abnormal uterus physiology	Pgr<tm1Bwo>/Pgr<tm1Bwo>	involves: 129S7/SvEvBrd	N	20029965
MGI:4429407	M	MP:0001922	reduced male fertility	Lep<ob>/Lep<ob>	involves: STOCK Mlph<ln> a Tgfa<wa1> Cdh23<v> Ednrb<s>	N	6393185
MGI:4429407	M	MP:0001925	male infertility	Lep<ob>/Lep<ob>	involves: STOCK Mlph<ln> a Tgfa<wa1> Cdh23<v> Ednrb<s>	N	6393185
MGI:4429407	F	MP:0001926	female infertility	Lep<ob>/Lep<ob>	involves: STOCK Mlph<ln> a Tgfa<wa1> Cdh23<v> Ednrb<s>	N	6393185
MGI:4429495	M	MP:0006380	abnormal spermatid morphology	Mcph1<tm1.2Kali>/Mcph1<tm1.2Kali>	involves: 129S7/SvEvBrd * C57BL/6J	N	20107607
MGI:4429495	M	MP:0014052	increased male germ cell apoptosis	Mcph1<tm1.2Kali>/Mcph1<tm1.2Kali>	involves: 129S7/SvEvBrd * C57BL/6J	N	20107607
MGI:4429495	M	MP:0005169	abnormal male meiosis	Mcph1<tm1.2Kali>/Mcph1<tm1.2Kali>	involves: 129S7/SvEvBrd * C57BL/6J	N	20107607
MGI:4429495	F	MP:0002777	absent ovarian follicles	Mcph1<tm1.2Kali>/Mcph1<tm1.2Kali>	involves: 129S7/SvEvBrd * C57BL/6J	N	20107607
MGI:4429495	M	MP:0004901	decreased male germ cell number	Mcph1<tm1.2Kali>/Mcph1<tm1.2Kali>	involves: 129S7/SvEvBrd * C57BL/6J	N	20107607
MGI:4429495	M	MP:0002216	abnormal seminiferous tubule morphology	Mcph1<tm1.2Kali>/Mcph1<tm1.2Kali>	involves: 129S7/SvEvBrd * C57BL/6J	N	20107607
MGI:4429495	F	MP:0001926	female infertility	Mcph1<tm1.2Kali>/Mcph1<tm1.2Kali>	involves: 129S7/SvEvBrd * C57BL/6J	N	20107607
MGI:4429495	M	MP:0008261	arrest of male meiosis	Mcph1<tm1.2Kali>/Mcph1<tm1.2Kali>	involves: 129S7/SvEvBrd * C57BL/6J	N	20107607
MGI:4429495	F	MP:0004856	decreased ovary weight	Mcph1<tm1.2Kali>/Mcph1<tm1.2Kali>	involves: 129S7/SvEvBrd * C57BL/6J	N	20107607
MGI:4429495	M	MP:0001147	small testis	Mcph1<tm1.2Kali>/Mcph1<tm1.2Kali>	involves: 129S7/SvEvBrd * C57BL/6J	N	20107607
MGI:4429495	M	MP:0001925	male infertility	Mcph1<tm1.2Kali>/Mcph1<tm1.2Kali>	involves: 129S7/SvEvBrd * C57BL/6J	N	20107607
MGI:4429607	F	MP:0009222	increased uterus tumor incidence	Msh2<tm1Htr>/Msh2<+>	involves: 129P2/OlaHsd	N	9443401
MGI:4429608	F	MP:0009222	increased uterus tumor incidence	Msh2<tm1Htr>/Msh2<tm1Htr>	involves: 129P2/OlaHsd * FVB	N	9443401
MGI:4429609	F	MP:0009222	increased uterus tumor incidence	Msh2<tm1Htr>/Msh2<tm1Htr>,Tap1<tm1Hpl>/Tap1<tm1Hpl>	involves: 129P2/OlaHsd * FVB	N	9443401
MGI:4429660	F	MP:0009082	uterus cyst	Drd2<tm1Low>/Drd2<tm1Low>	either: B6.129S2-Drd2<tm1Low> or (involves: 129S2/SvPas * C57BL/6)	N	9247267
MGI:4429660	F	MP:0002676	uterus hyperplasia	Drd2<tm1Low>/Drd2<tm1Low>	either: B6.129S2-Drd2<tm1Low> or (involves: 129S2/SvPas * C57BL/6)	N	9247267
MGI:4429660	F	MP:0009221	uterus adenomyosis	Drd2<tm1Low>/Drd2<tm1Low>	either: B6.129S2-Drd2<tm1Low> or (involves: 129S2/SvPas * C57BL/6)	N	9247267
MGI:4429660	F	MP:0009089	short uterine horn	Drd2<tm1Low>/Drd2<tm1Low>	either: B6.129S2-Drd2<tm1Low> or (involves: 129S2/SvPas * C57BL/6)	N	9247267
MGI:4429863	M	MP:0003402	decreased liver weight	Drd2<tm1Low>/Drd2<tm1Low>	B6.129S2-Drd2<tm1Low>/J	N	11897683
MGI:4429863	M	MP:0001258	decreased body length	Drd2<tm1Low>/Drd2<tm1Low>	B6.129S2-Drd2<tm1Low>/J	N	11897683
MGI:4429863	M	MP:0003109	short femur	Drd2<tm1Low>/Drd2<tm1Low>	B6.129S2-Drd2<tm1Low>/J	N	11897683
MGI:4429863	M	MP:0011939	increased food intake	Drd2<tm1Low>/Drd2<tm1Low>	B6.129S2-Drd2<tm1Low>/J	N	11897683
MGI:4429952	M	MP:0031629	abnormal mounting behavior	Chrm2<tm1Jwe>/Chrm2<tm1Jwe>	B6.129S4-Chrm2<tm1Jwe>	N	18382674
MGI:4429952	M	MP:0002566	abnormal sexual interaction	Chrm2<tm1Jwe>/Chrm2<tm1Jwe>	B6.129S4-Chrm2<tm1Jwe>	N	18382674
MGI:4429975	F	MP:0000198	decreased circulating phosphate level	Phex<Hyp>/Phex<Hyp>	B6.Cg-Phex<Hyp>/J	N	14751570
MGI:4429975	F	MP:0003718	maternal effect	Phex<Hyp>/Phex<Hyp>	B6.Cg-Phex<Hyp>/J	N	14751570
MGI:4429975	F	MP:0002759	abnormal caudal vertebrae morphology	Phex<Hyp>/Phex<Hyp>	B6.Cg-Phex<Hyp>/J	N	14751570
MGI:4429975	F	MP:0004652	small caudal vertebrae	Phex<Hyp>/Phex<Hyp>	B6.Cg-Phex<Hyp>/J	N	14751570
MGI:4429975	F	MP:0009445	osteomalacia	Phex<Hyp>/Phex<Hyp>	B6.Cg-Phex<Hyp>/J	N	14751570
MGI:4430075	M	MP:0001155	arrest of spermatogenesis	Tbc1d20<bs>/Tbc1d20<bs>	129S;AKR-Tbc1d20<bs>/J	N	14757819
MGI:4430075	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Tbc1d20<bs>/Tbc1d20<bs>	129S;AKR-Tbc1d20<bs>/J	N	24239381
MGI:4430075	M	MP:0004901	decreased male germ cell number	Tbc1d20<bs>/Tbc1d20<bs>	129S;AKR-Tbc1d20<bs>/J	N	24239381
MGI:4430075	M	MP:0008839	absent acrosome	Tbc1d20<bs>/Tbc1d20<bs>	129S;AKR-Tbc1d20<bs>/J	N	24239381
MGI:4430075	M	MP:0003631	nervous system phenotype	Tbc1d20<bs>/Tbc1d20<bs>	129S;AKR-Tbc1d20<bs>/J	Y	24239381
MGI:4430075	M	MP:0001147	small testis	Tbc1d20<bs>/Tbc1d20<bs>	129S;AKR-Tbc1d20<bs>/J	N	24239381
MGI:4430084	M	MP:0002717	abnormal male preputial gland morphology	Uaca<tm1Kiy>/Uaca<tm1Kiy>	B6.129P2-Uaca<tm1Kiy>	N	19637241
MGI:4430187	M	MP:0003599	large penis	Del(8A4-B3)7H/+	involves: 101/H * C3H/HeH	N	17584866
MGI:4430193	F	MP:0001405	impaired coordination	Dnase1l1<tm1Dkfz>/Dnase1l1<tm1Dkfz>	B6.129P2-Dnase1l1<tm1Dkfz>	N	MGI:4429693
MGI:4430235	F	MP:0004941	abnormal regulatory T cell morphology	Foxp3<tm7.2Ayr>/Foxp3<tm7.2Ayr>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	20072126
MGI:4430235	F	MP:0004974	decreased regulatory T cell number	Foxp3<tm7.2Ayr>/Foxp3<tm7.2Ayr>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	20072126
MGI:4430237	F	MP:0004974	decreased regulatory T cell number	Foxp3<tm7.2Ayr>/Foxp3<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	20072126
MGI:4430238	F	MP:0004974	decreased regulatory T cell number	Foxp3<tm6.2Ayr>/Foxp3<tm6.2Ayr>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	20072126
MGI:4430239	F	MP:0008894	abnormal intraepithelial T cell morphology	Foxp3<tm5.2Ayr>/Foxp3<tm5.2Ayr>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	20072126
MGI:4430239	F	MP:0004974	decreased regulatory T cell number	Foxp3<tm5.2Ayr>/Foxp3<tm5.2Ayr>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	20072126
MGI:4430239	F	MP:0005232	abnormal mesenteric lymph node morphology	Foxp3<tm5.2Ayr>/Foxp3<tm5.2Ayr>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	20072126
MGI:4430239	F	MP:0002145	abnormal T cell differentiation	Foxp3<tm5.2Ayr>/Foxp3<tm5.2Ayr>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	20072126
MGI:4430239	F	MP:0000696	abnormal Peyer's patch morphology	Foxp3<tm5.2Ayr>/Foxp3<tm5.2Ayr>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	20072126
MGI:4430239	F	MP:0002378	abnormal gut-associated lymphoid tissue morphology	Foxp3<tm5.2Ayr>/Foxp3<tm5.2Ayr>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	20072126
MGI:4430239	F	MP:0005015	increased T cell number	Foxp3<tm5.2Ayr>/Foxp3<tm5.2Ayr>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	N	20072126
MGI:4430249	M	MP:0008892	abnormal sperm flagellum morphology	Cyp17a1<tm1Vpap>/Cyp17a1<+>	chimera involves: 129X1/SvJ * C57BL/6	N	15890676
MGI:4430249	M	MP:0001922	reduced male fertility	Cyp17a1<tm1Vpap>/Cyp17a1<+>	chimera involves: 129X1/SvJ * C57BL/6	N	15890676
MGI:4430249	M	MP:0002675	asthenozoospermia	Cyp17a1<tm1Vpap>/Cyp17a1<+>	chimera involves: 129X1/SvJ * C57BL/6	N	15890676
MGI:4430330	F	MP:0001926	female infertility	Foxl2<tm4(cre)Tre>/Foxl2<tm4(cre)Tre>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20005806
MGI:4430330	F	MP:0001131	abnormal ovarian follicle morphology	Foxl2<tm4(cre)Tre>/Foxl2<tm4(cre)Tre>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20005806
MGI:4430330	F	MP:0001132	absent mature ovarian follicles	Foxl2<tm4(cre)Tre>/Foxl2<tm4(cre)Tre>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20005806
MGI:4430330	F	MP:0001127	small ovary	Foxl2<tm4(cre)Tre>/Foxl2<tm4(cre)Tre>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20005806
MGI:4430330	F	MP:0001129	impaired ovarian folliculogenesis	Foxl2<tm4(cre)Tre>/Foxl2<tm4(cre)Tre>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20005806
MGI:4430335	F	MP:0001126	abnormal ovary morphology	Gt(ROSA)26Sor<tm1(HBEGF)Awai>/Gt(ROSA)26Sor<tm1(HBEGF)Awai>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	20005806
MGI:4430335	F	MP:0031472	abnormal female germ cell apoptosis	Gt(ROSA)26Sor<tm1(HBEGF)Awai>/Gt(ROSA)26Sor<tm1(HBEGF)Awai>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	20005806
MGI:4430335	F	MP:0001131	abnormal ovarian follicle morphology	Gt(ROSA)26Sor<tm1(HBEGF)Awai>/Gt(ROSA)26Sor<tm1(HBEGF)Awai>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	20005806
MGI:4430335	F	MP:0031015	abnormal granulosa cell apoptosis	Gt(ROSA)26Sor<tm1(HBEGF)Awai>/Gt(ROSA)26Sor<tm1(HBEGF)Awai>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	20005806
MGI:4430336	F	MP:0004805	absent oocytes	Gt(ROSA)26Sor<tm2(DTA)Riet>/Gt(ROSA)26Sor<tm2(DTA)Riet>,Tg(Gdf9-icre)5092Coo/0	involves: 129P2/OlaHsd * C57BL/6	N	20005806
MGI:4430347	F	MP:0009661	abnormal pregnancy	Notch3<hpbk>/Notch3<hpbk>	C57BL/6J-Notch3<hpbk>/GrsrJ	N	MGI:4430322
MGI:4430347	M	MP:0003554	phimosis	Notch3<hpbk>/Notch3<hpbk>	C57BL/6J-Notch3<hpbk>/GrsrJ	N	MGI:4430322
MGI:4430347	M	MP:0001925	male infertility	Notch3<hpbk>/Notch3<hpbk>	C57BL/6J-Notch3<hpbk>/GrsrJ	N	MGI:4430322
MGI:4430366	M	MP:0011101	prenatal lethality, incomplete penetrance	Ar<Tfm> Eda<Ta-25H>/Y	involves: 101/H * C3H/HeH	N	2055107
MGI:4430366	M	MP:0001265	decreased body size	Ar<Tfm> Eda<Ta-25H>/Y	involves: 101/H * C3H/HeH	N	2055107
MGI:4430366	M	MP:0002789	male pseudohermaphroditism	Ar<Tfm> Eda<Ta-25H>/Y	involves: 101/H * C3H/HeH	N	2055107
MGI:4430366	M	MP:0002075	abnormal coat/hair pigmentation	Ar<Tfm> Eda<Ta-25H>/Y	involves: 101/H * C3H/HeH	N	2055107
MGI:4430366	M	MP:0000914	exencephaly	Ar<Tfm> Eda<Ta-25H>/Y	involves: 101/H * C3H/HeH	N	2055107
MGI:4430366	M	MP:0009659	striated fur	Ar<Tfm> Eda<Ta-25H>/Y	involves: 101/H * C3H/HeH	N	2055107
MGI:4430366	M	MP:0011088	neonatal lethality, incomplete penetrance	Ar<Tfm> Eda<Ta-25H>/Y	involves: 101/H * C3H/HeH	N	2055107
MGI:4430366	M	MP:0000372	irregular coat pigmentation	Ar<Tfm> Eda<Ta-25H>/Y	involves: 101/H * C3H/HeH	N	2055107
MGI:4430366	M	MP:0010231	transverse fur striping	Ar<Tfm> Eda<Ta-25H>/Y	involves: 101/H * C3H/HeH	N	2055107
MGI:4430485	M	MP:0001925	male infertility	Brca2<tm1Cbl>/Brca2<tm1Cbl>	either: (involves: 129S2/SvPas * C57BL/10) or (involves: 129S2/SvPas * C57BL/6 * DBA/2)	N	9398843
MGI:4430485	F	MP:0013236	ovary degeneration	Brca2<tm1Cbl>/Brca2<tm1Cbl>	either: (involves: 129S2/SvPas * C57BL/10) or (involves: 129S2/SvPas * C57BL/6 * DBA/2)	N	9398843
MGI:4430485	M	MP:0001147	small testis	Brca2<tm1Cbl>/Brca2<tm1Cbl>	either: (involves: 129S2/SvPas * C57BL/10) or (involves: 129S2/SvPas * C57BL/6 * DBA/2)	N	9398843
MGI:4430485	F	MP:0002777	absent ovarian follicles	Brca2<tm1Cbl>/Brca2<tm1Cbl>	either: (involves: 129S2/SvPas * C57BL/10) or (involves: 129S2/SvPas * C57BL/6 * DBA/2)	N	9398843
MGI:4430485	M	MP:0005159	azoospermia	Brca2<tm1Cbl>/Brca2<tm1Cbl>	either: (involves: 129S2/SvPas * C57BL/10) or (involves: 129S2/SvPas * C57BL/6 * DBA/2)	N	9398843
MGI:4430485	F	MP:0001127	small ovary	Brca2<tm1Cbl>/Brca2<tm1Cbl>	either: (involves: 129S2/SvPas * C57BL/10) or (involves: 129S2/SvPas * C57BL/6 * DBA/2)	N	9398843
MGI:4430562	F	MP:0001386	abnormal maternal nurturing	sps/sps	involves: C57BL/10Bg	N	MGI:80268
MGI:4430627	M	MP:0004909	increased seminal vesicle weight	Prlr<tm1Cnp>/Prlr<tm1Cnp>	involves: 129P2/OlaHsd * 129S2/SvPas	N	12810576
MGI:4430627	M	MP:0001922	reduced male fertility	Prlr<tm1Cnp>/Prlr<tm1Cnp>	involves: 129P2/OlaHsd * 129S2/SvPas	N	12810576
MGI:4430627	M	MP:0001168	abnormal prostate gland epithelium morphology	Prlr<tm1Cnp>/Prlr<tm1Cnp>	involves: 129P2/OlaHsd * 129S2/SvPas	N	12810576
MGI:4430627	M	MP:0031364	increased prostate gland ventral lobe weight	Prlr<tm1Cnp>/Prlr<tm1Cnp>	involves: 129P2/OlaHsd * 129S2/SvPas	N	12810576
MGI:4430627	M	MP:0005248	abnormal Harderian gland morphology	Prlr<tm1Cnp>/Prlr<tm1Cnp>	involves: 129P2/OlaHsd * 129S2/SvPas	N	11133844
MGI:4430627	M	MP:0001925	male infertility	Prlr<tm1Cnp>/Prlr<tm1Cnp>	involves: 129P2/OlaHsd * 129S2/SvPas	N	12810576
MGI:4430635	F	MP:0005668	decreased circulating leptin level	Prlr<tm1Cnp>/Prlr<tm1Cnp>	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	N	11159821
MGI:4430637	F	MP:0000628	abnormal mammary gland development	Prlr<tm1Cnp>/Prlr<+>	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	N	11445538
MGI:4430638	F	MP:0001884	mammary gland alveolar hyperplasia	Ifng<tm1Ts>/Ifng<tm1Ts>,Socs1<tm1Wehi>/Socs1<tm1Wehi>	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	N	11445538
MGI:4430638	F	MP:0001882	abnormal lactation	Ifng<tm1Ts>/Ifng<tm1Ts>,Socs1<tm1Wehi>/Socs1<tm1Wehi>	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	N	11445538
MGI:4430638	F	MP:0006269	abnormal mammary gland growth during pregnancy	Ifng<tm1Ts>/Ifng<tm1Ts>,Socs1<tm1Wehi>/Socs1<tm1Wehi>	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	N	11445538
MGI:4430869	M	MP:0004852	decreased testis weight	Kitl<tm2.1Pbes>/Kitl<tm2.1Pbes>	involves: 129S1/Sv * C57BL/6J * FVB/N	N	19874813
MGI:4430870	M	MP:0005159	azoospermia	Kitl<tm2.1Pbes>/Kitl<Sl>	involves: 129S1/Sv * C3H * C57BL/6J * FVB/N	N	19874813
MGI:4430871	M	MP:0005159	azoospermia	Kitl<tm3.1Pbes>/Kitl<tm3.1Pbes>	involves: 129S1/Sv * C57BL/6J * FVB/N	N	19874813
MGI:4430871	M	MP:0004852	decreased testis weight	Kitl<tm3.1Pbes>/Kitl<tm3.1Pbes>	involves: 129S1/Sv * C57BL/6J * FVB/N	N	19874813
MGI:4430871	M	MP:0001922	reduced male fertility	Kitl<tm3.1Pbes>/Kitl<tm3.1Pbes>	involves: 129S1/Sv * C57BL/6J * FVB/N	N	19874813
MGI:4430894	M	MP:0001925	male infertility	Abcg5<trac>/Abcg5<trac>	A/J-Abcg5<trac>	N	19846887
MGI:4430894	M	MP:0001156	abnormal spermatogenesis	Abcg5<trac>/Abcg5<trac>	A/J-Abcg5<trac>	N	19846887
MGI:4430894	F	MP:0001926	female infertility	Abcg5<trac>/Abcg5<trac>	A/J-Abcg5<trac>	N	19846887
MGI:4431013	M	MP:0010357	increased prostate gland tumor incidence	Tg(C3-1-TAg)cJeg/0	FVB/N-Tg(C3-1-TAg)cJeg	N	12810576
MGI:4431013	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(C3-1-TAg)cJeg/0	FVB/N-Tg(C3-1-TAg)cJeg	N	12810576
MGI:4431014	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Prlr<tm1Cnp>/Prlr<tm1Cnp>,Tg(C3-1-TAg)cJeg/0	involves: 129P2/OlaHsd * 129S2/SvPas * FVB/N	N	12810576
MGI:4431082	M	MP:0001925	male infertility	Ar<tm1Jdz>/Y,Tg(Abpa-cre)1Cmal/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	19574395
MGI:4431082	M	MP:0001156	abnormal spermatogenesis	Ar<tm1Jdz>/Y,Tg(Abpa-cre)1Cmal/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	19574395
MGI:4431082	M	MP:0002786	abnormal Leydig cell morphology	Ar<tm1Jdz>/Y,Tg(Abpa-cre)1Cmal/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	19574395
MGI:4431082	M	MP:0005378	growth/size/body region phenotype	Ar<tm1Jdz>/Y,Tg(Abpa-cre)1Cmal/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	Y	19574395
MGI:4431082	M	MP:0001153	small seminiferous tubules	Ar<tm1Jdz>/Y,Tg(Abpa-cre)1Cmal/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	19574395
MGI:4431082	M	MP:0004852	decreased testis weight	Ar<tm1Jdz>/Y,Tg(Abpa-cre)1Cmal/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	19574395
MGI:4431082	M	MP:0013598	Leydig cell hypertrophy	Ar<tm1Jdz>/Y,Tg(Abpa-cre)1Cmal/0	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	19574395
MGI:4431083	M	MP:0004852	decreased testis weight	Ar<tm1Jdz>/Y,Tg(Abpa-cre)1Cmal/Tg(Abpa-cre)1Cmal	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	19574395
MGI:4431083	M	MP:0001155	arrest of spermatogenesis	Ar<tm1Jdz>/Y,Tg(Abpa-cre)1Cmal/Tg(Abpa-cre)1Cmal	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	19574395
MGI:4431083	M	MP:0001153	small seminiferous tubules	Ar<tm1Jdz>/Y,Tg(Abpa-cre)1Cmal/Tg(Abpa-cre)1Cmal	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	19574395
MGI:4431083	M	MP:0001146	abnormal testis morphology	Ar<tm1Jdz>/Y,Tg(Abpa-cre)1Cmal/Tg(Abpa-cre)1Cmal	involves: 129X1/SvJ * C57BL/6 * DBA/2	N	19574395
MGI:4431084	M	MP:0004852	decreased testis weight	Ar<tm1Jdz>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>,Tg(Abpa-cre)1Cmal/0	involves: 129X1/SvJ * C57BL/6 * DBA/2 * SJL	N	19574395
MGI:4431116	M	MP:0001925	male infertility	Ar<tm1Jdz>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129X1/SvJ * C57BL/6 * SJL	N	19574395
MGI:4431116	M	MP:0013598	Leydig cell hypertrophy	Ar<tm1Jdz>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129X1/SvJ * C57BL/6 * SJL	N	19574395
MGI:4431116	M	MP:0001155	arrest of spermatogenesis	Ar<tm1Jdz>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129X1/SvJ * C57BL/6 * SJL	N	19574395
MGI:4431116	M	MP:0002786	abnormal Leydig cell morphology	Ar<tm1Jdz>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129X1/SvJ * C57BL/6 * SJL	N	19574395
MGI:4431116	M	MP:0001153	small seminiferous tubules	Ar<tm1Jdz>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129X1/SvJ * C57BL/6 * SJL	N	19574395
MGI:4431116	M	MP:0004852	decreased testis weight	Ar<tm1Jdz>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129X1/SvJ * C57BL/6 * SJL	N	19574395
MGI:4431116	M	MP:0005378	growth/size/body region phenotype	Ar<tm1Jdz>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129X1/SvJ * C57BL/6 * SJL	Y	19574395
MGI:4431166	M	MP:0004852	decreased testis weight	Ar<tm1Jdz>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<Tg(AMH-cre)1Flor>	involves: 129X1/SvJ * C57BL/6 * SJL	N	19574395
MGI:4431166	M	MP:0001153	small seminiferous tubules	Ar<tm1Jdz>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<Tg(AMH-cre)1Flor>	involves: 129X1/SvJ * C57BL/6 * SJL	N	19574395
MGI:4431166	M	MP:0001155	arrest of spermatogenesis	Ar<tm1Jdz>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<Tg(AMH-cre)1Flor>	involves: 129X1/SvJ * C57BL/6 * SJL	N	19574395
MGI:4431167	M	MP:0004852	decreased testis weight	Ar<tm1Jdz>/Y,Tg(CMV-cre)1Cgn/0	involves: 129X1/SvJ * BALB/cJ	N	19574395
MGI:4431192	M	MP:0002687	oligozoospermia	Insl6<tm1Imad>/Insl6<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1	N	19520787
MGI:4431192	M	MP:0001922	reduced male fertility	Insl6<tm1Imad>/Insl6<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1	N	19520787
MGI:4431192	M	MP:0001156	abnormal spermatogenesis	Insl6<tm1Imad>/Insl6<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1	N	19520787
MGI:4431192	M	MP:0005159	azoospermia	Insl6<tm1Imad>/Insl6<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1	N	19520787
MGI:4431192	M	MP:0006362	abnormal male germ cell morphology	Insl6<tm1Imad>/Insl6<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1	N	19520787
MGI:4431192	M	MP:0001925	male infertility	Insl6<tm1Imad>/Insl6<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1	N	19520787
MGI:4431192	M	MP:0008280	abnormal male germ cell apoptosis	Insl6<tm1Imad>/Insl6<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1	N	19520787
MGI:4431192	M	MP:0002675	asthenozoospermia	Insl6<tm1Imad>/Insl6<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1	N	19520787
MGI:4431192	M	MP:0001147	small testis	Insl6<tm1Imad>/Insl6<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1	N	19520787
MGI:4431220	F	MP:0003116	rickets	Phex<Hyp>/Phex<+>,Tg(Bglap2-Phex)1Ldq/?	involves: C57BL/6J	N	11713245
MGI:4431220	F	MP:0009445	osteomalacia	Phex<Hyp>/Phex<+>,Tg(Bglap2-Phex)1Ldq/?	involves: C57BL/6J	N	11713245
MGI:4431220	F	MP:0000198	decreased circulating phosphate level	Phex<Hyp>/Phex<+>,Tg(Bglap2-Phex)1Ldq/?	involves: C57BL/6J	N	11713245
MGI:4431220	F	MP:0004016	decreased bone mass	Phex<Hyp>/Phex<+>,Tg(Bglap2-Phex)1Ldq/?	involves: C57BL/6J	N	11713245
MGI:4431220	F	MP:0002896	abnormal bone mineralization	Phex<Hyp>/Phex<+>,Tg(Bglap2-Phex)1Ldq/?	involves: C57BL/6J	N	11713245
MGI:4436852	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm4(Ple88-EGFP)Ems>/Y	B6.129P2(Cg)-Hprt1<tm4(Ple88-EGFP)Ems>/Mmjax	N	MGI:3835781
MGI:4436853	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm7(Ple185-EGFP)Ems>/Y	B6.129P2(Cg)-Hprt1<tm7(Ple185-EGFP)Ems>/Mmjax	N	MGI:3835781
MGI:4436854	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm8(Ple151-EGFP)Ems>/Y	B6.129P2(Cg)-Hprt1<tm8(Ple151-EGFP)Ems>/Mmjax	N	MGI:3835781
MGI:4436855	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm9(Ple178-EGFP/cre)Ems>/Y	B6.129P2(129S4)-Hprt1<tm9(Ple178-EGFP/cre)Ems>	N	MGI:3835781
MGI:4436856	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm11(Ple176-EGFP/cre)Ems>/Y	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	MGI:3835781
MGI:4436857	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm10(Ple162-EGFP/cre)Ems>/Y	B6.129P2(129S4)-Hprt1<tm10(Ple162-EGFP/cre)Ems>	N	MGI:3835781
MGI:4436858	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm12(Ple177-EGFP/cre)Ems>/Y	B6.129P2(129S4)-Hprt1<tm12(Ple177-EGFP/cre)Ems>	N	MGI:3835781
MGI:4436861	F	MP:0002169	no abnormal phenotype detected	Foxp3<tm8Ayr>/Foxp3<+>	B6.129-Foxp3<tm8Ayr>	N	17220874
MGI:4436862	M	MP:0002083	premature death	Foxp3<tm8Ayr>/Y	B6.129-Foxp3<tm8Ayr>	N	17220874
MGI:4436862	M	MP:0001844	autoimmune response	Foxp3<tm8Ayr>/Y	B6.129-Foxp3<tm8Ayr>	N	17220874
MGI:4437060	M	MP:0001925	male infertility	Kcnu1<tm1Cmsa>/Kcnu1<tm1Cmsa>	Not Specified	N	20138882
MGI:4437060	M	MP:0004542	impaired acrosome reaction	Kcnu1<tm1Cmsa>/Kcnu1<tm1Cmsa>	Not Specified	N	20138882
MGI:4437060	M	MP:0020451	decreased sperm progressive motility	Kcnu1<tm1Cmsa>/Kcnu1<tm1Cmsa>	Not Specified	N	20138882
MGI:4437060	M	MP:0003666	impaired sperm capacitation	Kcnu1<tm1Cmsa>/Kcnu1<tm1Cmsa>	Not Specified	N	20138882
MGI:4437119	F	MP:0001011	abnormal superior cervical ganglion morphology	Maged1<tm1.1Urfm>/Maged1<tm1.1Urfm>	B6.129P2-Maged1<tm1.1Urfm>	N	18772898
MGI:4437119	F	MP:0008859	abnormal hair cycle catagen phase	Maged1<tm1.1Urfm>/Maged1<tm1.1Urfm>	B6.129P2-Maged1<tm1.1Urfm>	N	18772898
MGI:4437119	F	MP:0009253	abnormal sympathetic neuron physiology	Maged1<tm1.1Urfm>/Maged1<tm1.1Urfm>	B6.129P2-Maged1<tm1.1Urfm>	N	18772898
MGI:4437119	F	MP:0003204	decreased neuron apoptosis	Maged1<tm1.1Urfm>/Maged1<tm1.1Urfm>	B6.129P2-Maged1<tm1.1Urfm>	N	18772898
MGI:4437119	F	MP:0003631	nervous system phenotype	Maged1<tm1.1Urfm>/Maged1<tm1.1Urfm>	B6.129P2-Maged1<tm1.1Urfm>	Y	18772898
MGI:4437123	F	MP:0008752	abnormal tumor necrosis factor level	Maged1<tm1.1Urfm>/Maged1<tm1.1Urfm>	involves: 129P2/OlaHsd	N	20133718
MGI:4437123	F	MP:0005253	abnormal eye physiology	Maged1<tm1.1Urfm>/Maged1<tm1.1Urfm>	involves: 129P2/OlaHsd	N	20133718
MGI:4437127	M	MP:0001922	reduced male fertility	Adam24<tm1Pmkf>/Adam24<tm1Pmkf>	involves: C57BL/6J	N	19670298
MGI:4437258	F	MP:0001144	vagina atresia	Dhx58<tm1Aki>/Dhx58<tm1Aki>	involves: 129/Sv * C57BL/6	N	20080593
MGI:4437258	F	MP:0004906	enlarged uterus	Dhx58<tm1Aki>/Dhx58<tm1Aki>	involves: 129/Sv * C57BL/6	N	20080593
MGI:4437295	F	MP:0012411	increased granulosa cell tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J	N	19819941
MGI:4437296	F	MP:0012411	increased granulosa cell tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2.1Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J	N	19819941
MGI:4437297	F	MP:0012411	increased granulosa cell tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Zuk>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J	N	19819941
MGI:4437461	F	MP:0003579	increased ovarian carcinoma incidence	Rb1<tm2Brn>/Rb1<tm2Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd	N	12839925
MGI:4437461	F	MP:0008000	increased ovary tumor incidence	Rb1<tm2Brn>/Rb1<tm2Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd	N	12839925
MGI:4437568	M	MP:0003864	abnormal midbrain development	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0004096	abnormal midbrain-hindbrain boundary development	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0009988	abnormal cerebellum vermis lobule I morphology	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0009989	abnormal cerebellum vermis lobule II morphology	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0001524	impaired limb coordination	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0000885	ectopic Purkinje cell	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0009964	abnormal cerebellum lobule morphology	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0009990	abnormal cerebellum vermis lobule III morphology	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0004097	abnormal cerebellar cortex morphology	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0009038	decreased inferior colliculus size	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0001405	impaired coordination	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0000913	abnormal brain development	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0002152	abnormal brain morphology	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0001488	increased startle reflex	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0006097	abnormal cerebellar lobule formation	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0001399	hyperactivity	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0000872	abnormal cerebellum external granule cell layer morphology	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0009267	abnormal cerebellum fissure morphology	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0002063	abnormal learning/memory/conditioning	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0012132	abnormal midbrain-hindbrain boundary morphology	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0005369	muscle phenotype	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	Y	20181585
MGI:4437568	M	MP:0002804	abnormal motor learning	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437568	M	MP:0006104	abnormal tectum morphology	Mid1<tm1Mero>/Y	B6.Cg-Mid1<tm1Mero>	N	20181585
MGI:4437603	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Ext1<tm1Vcs>/Ext1<+>,Hprt1<tm1(CAG-cre)Mnn>/Hprt1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	20080592
MGI:4437730	M	MP:0001922	reduced male fertility	t<w82>/t<w2>	Not Specified	N	15722415
MGI:4437739	F	MP:0000630	mammary gland hyperplasia	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Tg(Wnt1)1Hev/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	10213494
MGI:4437739	F	MP:0001884	mammary gland alveolar hyperplasia	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Tg(Wnt1)1Hev/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	10213494
MGI:4437739	F	MP:0001885	mammary gland duct hyperplasia	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Tg(Wnt1)1Hev/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	10213494
MGI:4437739	F	MP:0000628	abnormal mammary gland development	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Tg(Wnt1)1Hev/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	10213494
MGI:4437740	F	MP:0000630	mammary gland hyperplasia	Tg(Wnt1)1Hev/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	10213494
MGI:4437740	F	MP:0001885	mammary gland duct hyperplasia	Tg(Wnt1)1Hev/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	10213494
MGI:4437740	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(Wnt1)1Hev/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	10213494
MGI:4437741	F	MP:0000628	abnormal mammary gland development	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	10213494
MGI:4437892	F	MP:0004894	uterus atrophy	Apoe<tm1Bres>/Apoe<tm1Bres>,Esr1<tm1Ksk>/Esr1<tm1Ksk>	B6.129P2-Apoe<tm1Bres> Esr1<tm1Ksk>	N	11160157
MGI:4438040	F	MP:0000628	abnormal mammary gland development	Esr1<tm1Ksk>/Esr1<tm1Ksk>,Tg(MMTV-Erbb2)NK1Mul/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	12019156
MGI:4438260	F	MP:0002577	reduced enamel thickness	Amelx<Rgsc888>/Amelx<+>	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438260	F	MP:0004830	short incisors	Amelx<Rgsc888>/Amelx<+>	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438260	F	MP:0030089	short lower incisors	Amelx<Rgsc888>/Amelx<+>	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438260	F	MP:0002650	abnormal ameloblast morphology	Amelx<Rgsc888>/Amelx<+>	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438260	F	MP:0030450	abnormal enamel mineralization	Amelx<Rgsc888>/Amelx<+>	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438260	F	MP:0002649	abnormal enamel rod pattern	Amelx<Rgsc888>/Amelx<+>	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438260	F	MP:0002576	abnormal enamel morphology	Amelx<Rgsc888>/Amelx<+>	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438260	F	MP:0000126	brittle teeth	Amelx<Rgsc888>/Amelx<+>	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438260	F	MP:0005358	abnormal incisor morphology	Amelx<Rgsc888>/Amelx<+>	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438260	F	MP:0010096	abnormal incisor color	Amelx<Rgsc888>/Amelx<+>	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438260	F	MP:0030090	short upper incisors	Amelx<Rgsc888>/Amelx<+>	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0002689	abnormal molar morphology	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0030460	enamel pits	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0005358	abnormal incisor morphology	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0004830	short incisors	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0010096	abnormal incisor color	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0002649	abnormal enamel rod pattern	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0002650	abnormal ameloblast morphology	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0030450	abnormal enamel mineralization	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0030050	large mandible	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0002576	abnormal enamel morphology	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0030089	short lower incisors	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0000458	abnormal mandible morphology	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0030457	abnormal molar cusp morphology	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0030458	abnormal tooth wear	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0030090	short upper incisors	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0000116	abnormal tooth development	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438261	M	MP:0000126	brittle teeth	Amelx<Rgsc888>/Y	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438262	F	MP:0002650	abnormal ameloblast morphology	Amelx<Rgsc888>/Amelx<Rgsc888>	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438262	F	MP:0002576	abnormal enamel morphology	Amelx<Rgsc888>/Amelx<Rgsc888>	involves: C57BL/6JJcl * DBA/2J	N	20067920
MGI:4438263	F	MP:0008256	abnormal myometrium morphology	Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Sprr2f-cre)1Dcas/0	involves: 129S6/SvEvTac * FVB/N	N	20142330
MGI:4438263	F	MP:0004904	increased uterus weight	Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Sprr2f-cre)1Dcas/0	involves: 129S6/SvEvTac * FVB/N	N	20142330
MGI:4438263	F	MP:0004902	abnormal uterus size	Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Sprr2f-cre)1Dcas/0	involves: 129S6/SvEvTac * FVB/N	N	20142330
MGI:4438263	F	MP:0004868	increased endometrial carcinoma incidence	Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Sprr2f-cre)1Dcas/0	involves: 129S6/SvEvTac * FVB/N	N	20142330
MGI:4438774	F	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>,Tg(TcraTcrb)425Cbn/?	involves: 129S6/SvEvTac * C57BL/6	N	20153220
MGI:4438775	F	MP:0005078	abnormal cytotoxic T cell physiology	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	involves: 129S6/SvEvTac	N	22683123
MGI:4438775	F	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	involves: 129S6/SvEvTac	N	20153220
MGI:4438775	F	MP:0010084	abnormal long lived plasma cell morphology	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	involves: 129S6/SvEvTac	N	20153220
MGI:4438775	F	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	involves: 129S6/SvEvTac	N	20153220
MGI:4438775	F	MP:0008036	abnormal NK T cell morphology	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	involves: 129S6/SvEvTac	N	23430111
MGI:4438775	F	MP:0009058	decreased interleukin-21 secretion	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	involves: 129S6/SvEvTac	N	20153220
MGI:4438775	F	MP:0001805	decreased IgG level	Sh2d1a<tm1Pls>/Sh2d1a<tm1Pls>	involves: 129S6/SvEvTac	N	20153220
MGI:4438921	M	MP:0002574	increased vertical activity	Srr<tm1.2Jtc>/Srr<tm1.2Jtc>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	19065142
MGI:4438921	F	MP:0002797	increased thigmotaxis	Srr<tm1.2Jtc>/Srr<tm1.2Jtc>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	19065142
MGI:4438921	M	MP:0008432	abnormal long-term spatial reference memory	Srr<tm1.2Jtc>/Srr<tm1.2Jtc>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	19065142
MGI:4438921	M	MP:0001399	hyperactivity	Srr<tm1.2Jtc>/Srr<tm1.2Jtc>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	19065142
MGI:4439300	F	MP:0008000	increased ovary tumor incidence	Tg(CAG-lacZ,-SV40)#Bcv/0	involves: FVB/N	N	20056833
MGI:4439300	F	MP:0003579	increased ovarian carcinoma incidence	Tg(CAG-lacZ,-SV40)#Bcv/0	involves: FVB/N	N	20056833
MGI:4439310	F	MP:0031422	failure of superovulation	Pgr<tm4.2Lyd>/Pgr<tm4.2Lyd>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * FVB/N	N	20029965
MGI:4439310	F	MP:0001881	abnormal mammary gland physiology	Pgr<tm4.2Lyd>/Pgr<tm4.2Lyd>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * FVB/N	N	20029965
MGI:4439310	F	MP:0009671	abnormal uterus physiology	Pgr<tm4.2Lyd>/Pgr<tm4.2Lyd>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * FVB/N	N	20029965
MGI:4439339	F	MP:0006270	abnormal mammary gland growth during lactation	Agap2<tm1.1Kye>/Agap2<tm1.1Kye>	involves: C57BL/6	N	20075866
MGI:4439339	F	MP:0004047	abnormal milk composition	Agap2<tm1.1Kye>/Agap2<tm1.1Kye>	involves: C57BL/6	N	20075866
MGI:4439339	F	MP:0010249	lactation failure	Agap2<tm1.1Kye>/Agap2<tm1.1Kye>	involves: C57BL/6	N	20075866
MGI:4439339	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Agap2<tm1.1Kye>/Agap2<tm1.1Kye>	involves: C57BL/6	N	20075866
MGI:4439339	F	MP:0014126	increased mammary gland apoptosis	Agap2<tm1.1Kye>/Agap2<tm1.1Kye>	involves: C57BL/6	N	20075866
MGI:4439339	F	MP:0009506	abnormal mammary gland alveolus morphology	Agap2<tm1.1Kye>/Agap2<tm1.1Kye>	involves: C57BL/6	N	20075866
MGI:4439381	M	MP:0003631	nervous system phenotype	Cnga2<tm2Reed>/Y	involves: 129/Sv * BALB/cJ	Y	11257220
MGI:4439381	M	MP:0010055	abnormal sensory neuron physiology	Cnga2<tm2Reed>/Y	involves: 129/Sv * BALB/cJ	N	11257220
MGI:4439381	M	MP:0001983	abnormal olfactory system physiology	Cnga2<tm2Reed>/Y	involves: 129/Sv * BALB/cJ	N	11257220
MGI:4439394	M	MP:0001147	small testis	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	F	MP:0004856	decreased ovary weight	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	M	MP:0001925	male infertility	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	M	MP:0006379	abnormal spermatocyte morphology	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	M	MP:0009199	abnormal external male genitalia morphology	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	M	MP:0004930	small epididymis	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	F	MP:0001926	female infertility	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	F	MP:0009209	abnormal internal female genitalia morphology	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	M	MP:0004852	decreased testis weight	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	M	MP:0009205	abnormal internal male genitalia morphology	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	F	MP:0009081	thin uterus	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	M	MP:0002716	small male preputial gland	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	M	MP:0005188	small penis	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	M	MP:0001146	abnormal testis morphology	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	F	MP:0003699	abnormal female reproductive system physiology	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	M	MP:0002216	abnormal seminiferous tubule morphology	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	F	MP:0009009	absent estrous cycle	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	M	MP:0001153	small seminiferous tubules	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	F	MP:0001143	constricted vagina orifice	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	M	MP:0001157	small seminal vesicle	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	F	MP:0001126	abnormal ovary morphology	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	F	MP:0001129	impaired ovarian folliculogenesis	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	F	MP:0031239	increased atretic ovarian follicle number	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4439394	F	MP:0001134	absent corpus luteum	Gnrhr<Gt(181A6)Cmhd>/Gnrhr<Gt(181A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	20068010
MGI:4440459	M	MP:0005530	decreased renal vascular resistance	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	14718366
MGI:4440459	M	MP:0003957	abnormal nitric oxide homeostasis	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	14718366
MGI:4440459	M	MP:0002128	abnormal blood circulation	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	18596078
MGI:4440459	M	MP:0005367	renal/urinary system phenotype	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	Y	14718366
MGI:4440459	M	MP:0006316	increased urine sodium level	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	14718366
MGI:4440459	M	MP:0006317	decreased urine sodium level	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	18596078
MGI:4440459	M	MP:0011470	increased urine creatinine level	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	14718366
MGI:4440459	M	MP:0010759	decreased right ventricle systolic pressure	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	18326795
MGI:4440459	M	MP:0003620	oliguria	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	18596078
MGI:4440459	M	MP:0000278	abnormal myocardial fiber morphology	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	18326795
MGI:4440459	M	MP:0005530	decreased renal vascular resistance	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	18596078
MGI:4440459	M	MP:0005385	cardiovascular system phenotype	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	Y	14718366
MGI:4440459	M	MP:0005525	increased renal plasma flow rate	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	14718366
MGI:4440459	M	MP:0005526	decreased renal plasma flow rate	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	18596078
MGI:4440459	M	MP:0005527	increased renal glomerular filtration rate	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	14718366
MGI:4440459	M	MP:0002207	abnormal long-term potentiation	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	19369559
MGI:4440459	M	MP:0001262	decreased body weight	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	18326795
MGI:4440459	M	MP:0011741	increased urine nitrite level	Cybb<tm1Din>/Y	B6.129S-Cybb<tm1Din>	N	14718366
MGI:4440461	M	MP:0005405	axon degeneration	Cybb<tm1Din>/Y,Tg(SOD1*G93A)<dl>1Gur/0	B6.Cg-Cybb<tm1Din> Tg(SOD1*G93A)<dl>1Gur	N	16877542
MGI:4440461	M	MP:0002229	neurodegeneration	Cybb<tm1Din>/Y,Tg(SOD1*G93A)<dl>1Gur/0	B6.Cg-Cybb<tm1Din> Tg(SOD1*G93A)<dl>1Gur	N	16877542
MGI:4440461	M	MP:0002862	abnormal righting response	Cybb<tm1Din>/Y,Tg(SOD1*G93A)<dl>1Gur/0	B6.Cg-Cybb<tm1Din> Tg(SOD1*G93A)<dl>1Gur	N	16877542
MGI:4440461	M	MP:0002083	premature death	Cybb<tm1Din>/Y,Tg(SOD1*G93A)<dl>1Gur/0	B6.Cg-Cybb<tm1Din> Tg(SOD1*G93A)<dl>1Gur	N	16877542
MGI:4440461	M	MP:0009399	increased skeletal muscle fiber size	Cybb<tm1Din>/Y,Tg(SOD1*G93A)<dl>1Gur/0	B6.Cg-Cybb<tm1Din> Tg(SOD1*G93A)<dl>1Gur	N	16877542
MGI:4440461	M	MP:0000753	paralysis	Cybb<tm1Din>/Y,Tg(SOD1*G93A)<dl>1Gur/0	B6.Cg-Cybb<tm1Din> Tg(SOD1*G93A)<dl>1Gur	N	16877542
MGI:4440591	F	MP:0001120	abnormal uterus morphology	Del(4C4-C5)1Lap/Del(4C4-C5)1Lap	involves: 129S6/SvEvTac	N	20173736
MGI:4440862	F	MP:0001140	abnormal vagina epithelium morphology	Rab25<tm1Jrgo>/Rab25<tm1Jrgo>	129-Rab25<tm1Jrgo>	N	20197623
MGI:4441278	F	MP:0001923	reduced female fertility	dde/dde	CByJ(Cg)-dde/GrsrJ	N	MGI:4441075
MGI:4441278	M	MP:0008280	abnormal male germ cell apoptosis	dde/dde	CByJ(Cg)-dde/GrsrJ	N	MGI:4441075
MGI:4441278	F	MP:0001386	abnormal maternal nurturing	dde/dde	CByJ(Cg)-dde/GrsrJ	N	MGI:4441075
MGI:4441278	M	MP:0001925	male infertility	dde/dde	CByJ(Cg)-dde/GrsrJ	N	MGI:4441075
MGI:4441291	F	MP:0001406	abnormal gait	Gla<tm1Kul>/Gla<tm1Kul>,Itpr1<wblo>/Itpr1<wblo>	B6;129-Gla<tm1Kul> Itpr1<wblo>/GrsrJ	N	MGI:4441074
MGI:4441292	M	MP:0001406	abnormal gait	Gla<tm1Kul>/Y,Itpr1<wblo>/Itpr1<wblo>	B6;129-Gla<tm1Kul> Itpr1<wblo>/GrsrJ	N	MGI:4441074
MGI:4442333	F	MP:0009092	endometrium hyperplasia	Pten<tm1.1Gle>/Pten<+>	involves: 129S6/SvEvTac * Black Swiss * FVB/N	N	20194734
MGI:4442333	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm1.1Gle>/Pten<+>	involves: 129S6/SvEvTac * Black Swiss * FVB/N	N	20194734
MGI:4442335	F	MP:0009092	endometrium hyperplasia	Pten<tm2.1Gle>/Pten<+>	involves: 129S6/SvEvTac * Black Swiss * FVB/N	N	20194734
MGI:4442335	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm2.1Gle>/Pten<+>	involves: 129S6/SvEvTac * Black Swiss * FVB/N	N	20194734
MGI:4442363	M	MP:0003026	decreased vasoconstriction	Arhgef1<tm1Rmt>/Arhgef1<tm1Rmt>,X/Tg(Myh11-icre/ERT2)1Soff	involves: C57BL/6 * FVB/N	N	20098430
MGI:4442363	M	MP:0001625	cardiac hypertrophy	Arhgef1<tm1Rmt>/Arhgef1<tm1Rmt>,X/Tg(Myh11-icre/ERT2)1Soff	involves: C57BL/6 * FVB/N	N	20098430
MGI:4442363	M	MP:0009866	abnormal aorta wall morphology	Arhgef1<tm1Rmt>/Arhgef1<tm1Rmt>,X/Tg(Myh11-icre/ERT2)1Soff	involves: C57BL/6 * FVB/N	N	20098430
MGI:4442363	M	MP:0000230	abnormal systemic arterial blood pressure	Arhgef1<tm1Rmt>/Arhgef1<tm1Rmt>,X/Tg(Myh11-icre/ERT2)1Soff	involves: C57BL/6 * FVB/N	N	20098430
MGI:4442363	M	MP:0008874	decreased physiological sensitivity to xenobiotic	Arhgef1<tm1Rmt>/Arhgef1<tm1Rmt>,X/Tg(Myh11-icre/ERT2)1Soff	involves: C57BL/6 * FVB/N	N	20098430
MGI:4442845	M	MP:0001925	male infertility	fl/fl	Not Specified	N	MGI:48715
MGI:4442845	F	MP:0001923	reduced female fertility	fl/fl	Not Specified	N	MGI:48715
MGI:4442853	F	MP:0001927	abnormal estrous cycle	Gpr149<tm1.1Zuk>/Gpr149<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	19887567
MGI:4442853	F	MP:0005410	abnormal fertilization	Gpr149<tm1.1Zuk>/Gpr149<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	19887567
MGI:4442853	F	MP:0001934	increased litter size	Gpr149<tm1.1Zuk>/Gpr149<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	19887567
MGI:4442853	F	MP:0031424	enhanced female fertility	Gpr149<tm1.1Zuk>/Gpr149<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	19887567
MGI:4442853	F	MP:0009017	prolonged estrus	Gpr149<tm1.1Zuk>/Gpr149<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	19887567
MGI:4442853	F	MP:0011128	increased tertiary ovarian follicle number	Gpr149<tm1.1Zuk>/Gpr149<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	19887567
MGI:4442853	F	MP:0031411	increased ovulation rate	Gpr149<tm1.1Zuk>/Gpr149<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	19887567
MGI:4442853	F	MP:0001130	abnormal ovarian folliculogenesis	Gpr149<tm1.1Zuk>/Gpr149<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	19887567
MGI:4442853	F	MP:0031383	increased secondary ovarian follicle number	Gpr149<tm1.1Zuk>/Gpr149<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	19887567
MGI:4442853	F	MP:0031421	increased superovulation rate	Gpr149<tm1.1Zuk>/Gpr149<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	19887567
MGI:4442853	F	MP:0005376	homeostasis/metabolism phenotype	Gpr149<tm1.1Zuk>/Gpr149<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	Y	19887567
MGI:4442854	F	MP:0031421	increased superovulation rate	Gpr149<tm1.1Zuk>/Gpr149<+>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	19887567
MGI:4442904	M	MP:0009280	decreased activated sperm motility	Agtpbp1<m2Btlr>/Agtpbp1<m2Btlr>	C57BL/6J-Agtpbp1<m2Btlr>	N	MGI:4442412
MGI:4442907	M	MP:0009280	decreased activated sperm motility	Spag9<m1Btlr>/Spag9<m1Btlr>	C57BL/6J-Spag9<m1Btlr>	N	MGI:4442423
MGI:4443004	F	MP:0009504	abnormal mammary gland epithelium morphology	Med1<tm2Rgr>/Med1<tm2Rgr>	B6.129P2-Med1<tm2Rgr>	N	20351249
MGI:4443004	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Med1<tm2Rgr>/Med1<tm2Rgr>	B6.129P2-Med1<tm2Rgr>	N	20351249
MGI:4443004	F	MP:0000662	abnormal branching of the mammary ductal tree	Med1<tm2Rgr>/Med1<tm2Rgr>	B6.129P2-Med1<tm2Rgr>	N	20351249
MGI:4443004	F	MP:0000628	abnormal mammary gland development	Med1<tm2Rgr>/Med1<tm2Rgr>	B6.129P2-Med1<tm2Rgr>	N	20351249
MGI:4443052	M	MP:0000920	abnormal myelination	Plp1<jp-msd>/Y	involves: BALB/c * C57BL/6J * C57BL/10	N	4815353
MGI:4443052	M	MP:0002083	premature death	Plp1<jp-msd>/Y	involves: BALB/c * C57BL/6J * C57BL/10	N	4815353
MGI:4443053	F	MP:0002083	premature death	Plp1<jp-msd>/Plp1<jp-msd>	involves: BALB/c * C57BL/6J * C57BL/10	N	4815353
MGI:4443053	F	MP:0000920	abnormal myelination	Plp1<jp-msd>/Plp1<jp-msd>	involves: BALB/c * C57BL/6J * C57BL/10	N	4815353
MGI:4443115	F	MP:0001121	uterus hypoplasia	Lmx1a<dr-6J>/Lmx1a<dr-6J>	C3H/HeJ-Lmx1a<dr-6J>	N	10444330
MGI:4443115	M	MP:0001925	male infertility	Lmx1a<dr-6J>/Lmx1a<dr-6J>	C3H/HeJ-Lmx1a<dr-6J>	N	10444330
MGI:4443115	F	MP:0001926	female infertility	Lmx1a<dr-6J>/Lmx1a<dr-6J>	C3H/HeJ-Lmx1a<dr-6J>	N	10444330
MGI:4443123	F	MP:0000921	demyelination	Plp1<jp-rsh>/Plp1<+>	either: STOCK Rb(1.3)1Bnr or (involves: BALB/c * DBA/2 * STOCK Rb(1.3)1Bnr)	N	1944806
MGI:4443123	F	MP:0000136	abnormal microglial cell morphology	Plp1<jp-rsh>/Plp1<+>	either: STOCK Rb(1.3)1Bnr or (involves: BALB/c * DBA/2 * STOCK Rb(1.3)1Bnr)	N	1944806
MGI:4443123	F	MP:0010160	increased oligodendrocyte number	Plp1<jp-rsh>/Plp1<+>	either: STOCK Rb(1.3)1Bnr or (involves: BALB/c * DBA/2 * STOCK Rb(1.3)1Bnr)	N	1944806
MGI:4443123	F	MP:0000953	abnormal oligodendrocyte morphology	Plp1<jp-rsh>/Plp1<+>	either: STOCK Rb(1.3)1Bnr or (involves: BALB/c * DBA/2 * STOCK Rb(1.3)1Bnr)	N	1944806
MGI:4443123	F	MP:0000920	abnormal myelination	Plp1<jp-rsh>/Plp1<+>	either: STOCK Rb(1.3)1Bnr or (involves: BALB/c * DBA/2 * STOCK Rb(1.3)1Bnr)	N	1944806
MGI:4443306	M	MP:0005159	azoospermia	Eif4g3<repro8>/Eif4g3<repro8>	involves: C3HeB/FeJ * C57BL/6J	N	20430745
MGI:4443306	M	MP:0014052	increased male germ cell apoptosis	Eif4g3<repro8>/Eif4g3<repro8>	involves: C3HeB/FeJ * C57BL/6J	N	20430745
MGI:4443306	M	MP:0004852	decreased testis weight	Eif4g3<repro8>/Eif4g3<repro8>	involves: C3HeB/FeJ * C57BL/6J	N	20430745
MGI:4443306	M	MP:0008261	arrest of male meiosis	Eif4g3<repro8>/Eif4g3<repro8>	involves: C3HeB/FeJ * C57BL/6J	N	20430745
MGI:4443307	M	MP:0001147	small testis	Eif4g3<Gt(XC431)Byg>/Eif4g3<Gt(XC431)Byg>	involves: 129P2/OlaHsd	N	20430745
MGI:4443308	M	MP:0008261	arrest of male meiosis	Eif4g3<Gt(XC431)Byg>/Eif4g3<repro8>	involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J	N	20430745
MGI:4443308	M	MP:0005159	azoospermia	Eif4g3<Gt(XC431)Byg>/Eif4g3<repro8>	involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J	N	20430745
MGI:4443323	M	MP:0000920	abnormal myelination	Plp1<jp-msd>/Y	involves: C57BL/10Sn * BALB/cJ	N	5433413
MGI:4443323	M	MP:0002064	seizures	Plp1<jp-msd>/Y	involves: C57BL/10Sn * BALB/cJ	N	5433413
MGI:4443323	M	MP:0000745	tremors	Plp1<jp-msd>/Y	involves: C57BL/10Sn * BALB/cJ	N	5433413
MGI:4443323	M	MP:0011085	postnatal lethality, complete penetrance	Plp1<jp-msd>/Y	involves: C57BL/10Sn * BALB/cJ	N	5433413
MGI:4443323	M	MP:0000921	demyelination	Plp1<jp-msd>/Y	involves: C57BL/10Sn * BALB/cJ	N	5433413
MGI:4450915	F	MP:0000195	decreased circulating calcium level	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0004993	decreased bone resorption	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0000135	decreased compact bone thickness	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0002968	increased circulating alkaline phosphatase level	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0003408	increased width of hypertrophic chondrocyte zone	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0011504	abnormal limb long bone morphology	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0001406	abnormal gait	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0030830	abnormal acetabulum morphology	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0009877	exostosis	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0020010	decreased bone mineral density of femur	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0004509	abnormal pelvic girdle bone morphology	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0000063	decreased bone mineral density	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0000198	decreased circulating phosphate level	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0009445	osteomalacia	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0002759	abnormal caudal vertebrae morphology	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0002896	abnormal bone mineralization	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0001541	abnormal osteoclast physiology	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0000133	abnormal long bone metaphysis morphology	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0003055	abnormal long bone epiphyseal plate morphology	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0003116	rickets	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0030876	abnormal costochondral joint morphology	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0003109	short femur	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450915	F	MP:0014322	short hindlimb	Phex<Ska1>/Phex<Ska1>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0004359	short ulna	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0005508	abnormal skeleton morphology	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0030830	abnormal acetabulum morphology	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0002968	increased circulating alkaline phosphatase level	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0000150	abnormal rib morphology	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0020010	decreased bone mineral density of femur	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0004355	short radius	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0004351	short humerus	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0001406	abnormal gait	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0009877	exostosis	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0000198	decreased circulating phosphate level	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0000063	decreased bone mineral density	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0002759	abnormal caudal vertebrae morphology	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0000135	decreased compact bone thickness	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0003109	short femur	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0030828	abnormal obturator foramen morphology	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0014322	short hindlimb	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0002765	short fibula	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0004338	small clavicle	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0011504	abnormal limb long bone morphology	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0002764	short tibia	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450916	F	MP:0004509	abnormal pelvic girdle bone morphology	Phex<Ska1>/Phex<+>	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0030830	abnormal acetabulum morphology	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0014322	short hindlimb	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0000198	decreased circulating phosphate level	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0003109	short femur	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0009877	exostosis	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0001406	abnormal gait	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0004351	short humerus	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0005508	abnormal skeleton morphology	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0004355	short radius	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0030828	abnormal obturator foramen morphology	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0004359	short ulna	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0004509	abnormal pelvic girdle bone morphology	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0000150	abnormal rib morphology	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0011504	abnormal limb long bone morphology	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0002764	short tibia	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0002968	increased circulating alkaline phosphatase level	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0000556	abnormal hindlimb morphology	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0004338	small clavicle	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0002759	abnormal caudal vertebrae morphology	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450917	M	MP:0002765	short fibula	Phex<Ska1>/Y	C57BL/6-Phex<Ska1>	N	12414538
MGI:4450924	M	MP:0008254	increased megakaryocyte cell number	Gata1<tm1Sho>/Y,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450924	M	MP:0000208	decreased hematocrit	Gata1<tm1Sho>/Y,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450924	M	MP:0002874	decreased hemoglobin content	Gata1<tm1Sho>/Y,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450924	M	MP:0002875	decreased erythrocyte cell number	Gata1<tm1Sho>/Y,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450924	M	MP:0000218	increased leukocyte cell number	Gata1<tm1Sho>/Y,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450924	M	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm1Sho>/Y,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450924	M	MP:0005505	thrombocytosis	Gata1<tm1Sho>/Y,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450925	F	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm1Sho>/Gata1<tm1Sho>,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450925	F	MP:0002874	decreased hemoglobin content	Gata1<tm1Sho>/Gata1<tm1Sho>,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450925	F	MP:0000218	increased leukocyte cell number	Gata1<tm1Sho>/Gata1<tm1Sho>,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450925	F	MP:0000208	decreased hematocrit	Gata1<tm1Sho>/Gata1<tm1Sho>,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450925	F	MP:0008254	increased megakaryocyte cell number	Gata1<tm1Sho>/Gata1<tm1Sho>,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450925	F	MP:0002875	decreased erythrocyte cell number	Gata1<tm1Sho>/Gata1<tm1Sho>,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450925	F	MP:0005505	thrombocytosis	Gata1<tm1Sho>/Gata1<tm1Sho>,Tg(Gata1*)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	N	19682090
MGI:4450926	M	MP:0005397	hematopoietic system phenotype	Gata1<tm1Sho>/Y,Tg(Gata1)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	Y	19682090
MGI:4450927	F	MP:0005397	hematopoietic system phenotype	Gata1<tm1Sho>/Gata1<tm1Sho>,Tg(Gata1)#Mym/0	involves: 129S4/SvJae * C57BL/6 * DBA/2J	Y	19682090
MGI:4450928	F	MP:0002123	abnormal definitive hematopoiesis	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450928	F	MP:0002417	abnormal megakaryocyte morphology	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450928	F	MP:0001577	anemia	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450928	F	MP:0002447	abnormal erythrocyte morphology	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450928	F	MP:0002874	decreased hemoglobin content	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450928	F	MP:0008254	increased megakaryocyte cell number	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450928	F	MP:0000218	increased leukocyte cell number	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450928	F	MP:0000245	abnormal erythropoiesis	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450928	F	MP:0008973	decreased erythroid progenitor cell number	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450928	F	MP:0002875	decreased erythrocyte cell number	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450928	F	MP:0005505	thrombocytosis	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450928	F	MP:0000208	decreased hematocrit	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450928	F	MP:0004720	abnormal platelet morphology	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450928	F	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0005505	thrombocytosis	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0002123	abnormal definitive hematopoiesis	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0002874	decreased hemoglobin content	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0008254	increased megakaryocyte cell number	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0001577	anemia	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0002417	abnormal megakaryocyte morphology	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0000208	decreased hematocrit	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0000218	increased leukocyte cell number	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0002875	decreased erythrocyte cell number	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0000245	abnormal erythropoiesis	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0008973	decreased erythroid progenitor cell number	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0004720	abnormal platelet morphology	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450929	M	MP:0002447	abnormal erythrocyte morphology	Gata1<tm1Mym>/Y,Tg(Gata1*)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	N	19682090
MGI:4450930	M	MP:0005397	hematopoietic system phenotype	Gata1<tm1Mym>/Y,Tg(Gata1)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	Y	19682090
MGI:4450931	F	MP:0005397	hematopoietic system phenotype	Gata1<tm1Mym>/Gata1<tm1Mym>,Tg(Gata1)#Mym/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	Y	19682090
MGI:4450979	F	MP:0011101	prenatal lethality, incomplete penetrance	Li/Li<+>	Not Specified	N	9467016
MGI:4450979	F	MP:0001262	decreased body weight	Li/Li<+>	Not Specified	N	9467016
MGI:4450979	F	MP:0009674	decreased birth weight	Li/Li<+>	Not Specified	N	9467016
MGI:4450979	F	MP:0009659	striated fur	Li/Li<+>	Not Specified	N	MGI:62139
MGI:4450979	F	MP:0011101	prenatal lethality, incomplete penetrance	Li/Li<+>	Not Specified	N	MGI:62139
MGI:4450979	F	MP:0009659	striated fur	Li/Li<+>	Not Specified	N	9467016
MGI:4450980	M	MP:0011091	prenatal lethality, complete penetrance	Li/Y	Not Specified	N	MGI:62139
MGI:4450980	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Li/Y	Not Specified	N	9467016
MGI:4450980	M	MP:0001698	decreased embryo size	Li/Y	Not Specified	N	9467016
MGI:4450981	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Stpy/Y	involves: 101/H * C3H/HeH	N	9467016
MGI:4450982	F	MP:0009674	decreased birth weight	Stpy/Stpy<+>	involves: 101/H * C3H/HeH	N	9467016
MGI:4450982	F	MP:0011101	prenatal lethality, incomplete penetrance	Stpy/Stpy<+>	involves: 101/H * C3H/HeH	N	9467016
MGI:4450982	F	MP:0009659	striated fur	Stpy/Stpy<+>	involves: 101/H * C3H/HeH	N	9467016
MGI:4450982	F	MP:0001262	decreased body weight	Stpy/Stpy<+>	involves: 101/H * C3H/HeH	N	9467016
MGI:4452137	F	MP:0009504	abnormal mammary gland epithelium morphology	Sfn<tm1Mul>/Sfn<tm1Mul>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	20439433
MGI:4452139	F	MP:0009503	abnormal mammary gland duct morphology	Sfn<tm1Mul>/Sfn<tm1Mul>,Tg(MMTV-cre)7Mul/0	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	20439433
MGI:4452139	F	MP:0009504	abnormal mammary gland epithelium morphology	Sfn<tm1Mul>/Sfn<tm1Mul>,Tg(MMTV-cre)7Mul/0	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	20439433
MGI:4452521	F	MP:0002988	decreased urine osmolality	Cldn2<tm1Muto>/Cldn2<tm1Muto>	involves: 129S4/SvJae * C57BL/6	N	20385797
MGI:4452521	F	MP:0006316	increased urine sodium level	Cldn2<tm1Muto>/Cldn2<tm1Muto>	involves: 129S4/SvJae * C57BL/6	N	20385797
MGI:4452521	F	MP:0005441	increased urine calcium level	Cldn2<tm1Muto>/Cldn2<tm1Muto>	involves: 129S4/SvJae * C57BL/6	N	20385797
MGI:4452521	F	MP:0001762	polyuria	Cldn2<tm1Muto>/Cldn2<tm1Muto>	involves: 129S4/SvJae * C57BL/6	N	20385797
MGI:4452521	F	MP:0010108	abnormal renal water reabsorption	Cldn2<tm1Muto>/Cldn2<tm1Muto>	involves: 129S4/SvJae * C57BL/6	N	20385797
MGI:4452521	F	MP:0010109	abnormal renal sodium reabsorption	Cldn2<tm1Muto>/Cldn2<tm1Muto>	involves: 129S4/SvJae * C57BL/6	N	20385797
MGI:4452521	F	MP:0005367	renal/urinary system phenotype	Cldn2<tm1Muto>/Cldn2<tm1Muto>	involves: 129S4/SvJae * C57BL/6	Y	20385797
MGI:4452521	F	MP:0010107	abnormal renal reabsorption	Cldn2<tm1Muto>/Cldn2<tm1Muto>	involves: 129S4/SvJae * C57BL/6	N	20385797
MGI:4453205	F	MP:0001923	reduced female fertility	Tex19.1<tm1Hjc>/Tex19.1<tm1Hjc>	involves: 129P2/OlaHsd * CD-1	N	18802469
MGI:4453205	M	MP:0003698	abnormal male reproductive system physiology	Tex19.1<tm1Hjc>/Tex19.1<tm1Hjc>	involves: 129P2/OlaHsd * CD-1	N	18802469
MGI:4453205	M	MP:0014052	increased male germ cell apoptosis	Tex19.1<tm1Hjc>/Tex19.1<tm1Hjc>	involves: 129P2/OlaHsd * CD-1	N	18802469
MGI:4453205	M	MP:0004901	decreased male germ cell number	Tex19.1<tm1Hjc>/Tex19.1<tm1Hjc>	involves: 129P2/OlaHsd * CD-1	N	18802469
MGI:4453205	M	MP:0002216	abnormal seminiferous tubule morphology	Tex19.1<tm1Hjc>/Tex19.1<tm1Hjc>	involves: 129P2/OlaHsd * CD-1	N	18802469
MGI:4453205	M	MP:0002687	oligozoospermia	Tex19.1<tm1Hjc>/Tex19.1<tm1Hjc>	involves: 129P2/OlaHsd * CD-1	N	18802469
MGI:4453205	M	MP:0001156	abnormal spermatogenesis	Tex19.1<tm1Hjc>/Tex19.1<tm1Hjc>	involves: 129P2/OlaHsd * CD-1	N	18802469
MGI:4453205	M	MP:0005169	abnormal male meiosis	Tex19.1<tm1Hjc>/Tex19.1<tm1Hjc>	involves: 129P2/OlaHsd * CD-1	N	18802469
MGI:4453205	M	MP:0001922	reduced male fertility	Tex19.1<tm1Hjc>/Tex19.1<tm1Hjc>	involves: 129P2/OlaHsd * CD-1	N	18802469
MGI:4453205	M	MP:0004852	decreased testis weight	Tex19.1<tm1Hjc>/Tex19.1<tm1Hjc>	involves: 129P2/OlaHsd * CD-1	N	18802469
MGI:4453205	M	MP:0001147	small testis	Tex19.1<tm1Hjc>/Tex19.1<tm1Hjc>	involves: 129P2/OlaHsd * CD-1	N	18802469
MGI:4453575	M	MP:0014052	increased male germ cell apoptosis	Kdm3a<tm1Jxu>/Kdm3a<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	19910458
MGI:4453575	M	MP:0001147	small testis	Kdm3a<tm1Jxu>/Kdm3a<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	19910458
MGI:4453575	M	MP:0001156	abnormal spermatogenesis	Kdm3a<tm1Jxu>/Kdm3a<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	19910458
MGI:4453575	M	MP:0006380	abnormal spermatid morphology	Kdm3a<tm1Jxu>/Kdm3a<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	19910458
MGI:4453575	M	MP:0004852	decreased testis weight	Kdm3a<tm1Jxu>/Kdm3a<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	19910458
MGI:4453575	M	MP:0001925	male infertility	Kdm3a<tm1Jxu>/Kdm3a<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	19910458
MGI:4453575	M	MP:0001932	abnormal spermiogenesis	Kdm3a<tm1Jxu>/Kdm3a<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	19910458
MGI:4453575	M	MP:0002687	oligozoospermia	Kdm3a<tm1Jxu>/Kdm3a<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	19910458
MGI:4453853	F	MP:0008174	decreased follicular B cell number	Btk<xid>/Btk<xid>,Ikzf3<tm1Kge>/Ikzf3<tm1Kge>	involves: 129S4/SvJae * CBA/CaHN	N	11371362
MGI:4453854	M	MP:0008174	decreased follicular B cell number	Btk<xid>/Y,Ikzf3<tm1Kge>/Ikzf3<tm1Kge>	involves: 129S4/SvJae * CBA/CaHN	N	11371362
MGI:4453871	M	MP:0004184	abnormal baroreceptor physiology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	12154115
MGI:4453871	M	MP:0006319	abnormal epididymal fat pad morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0000521	abnormal kidney cortex morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	9551401
MGI:4453871	M	MP:0008263	abnormal hippocampus CA1 region morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	11384784
MGI:4453871	M	MP:0010009	abnormal piriform cortex morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	11384784
MGI:4453871	M	MP:0005659	decreased susceptibility to diet-induced obesity	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0001431	abnormal eating behavior	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0031413	abnormal skeletal muscle triglyceride level	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0005601	increased angiogenesis	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	14597675
MGI:4453871	M	MP:0011371	decreased kidney apoptosis	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	9551401
MGI:4453871	M	MP:0003215	renal interstitial fibrosis	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	9551401
MGI:4453871	M	MP:0005667	abnormal circulating leptin level	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0010182	decreased susceptibility to weight gain	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0004889	increased energy expenditure	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0002078	abnormal glucose homeostasis	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0000818	abnormal amygdala morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	11384784
MGI:4453871	M	MP:0008873	increased physiological sensitivity to xenobiotic	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	12154115
MGI:4453871	M	MP:0003638	abnormal response/metabolism to endogenous compounds	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0006274	abnormal urine sodium level	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	10620200
MGI:4453871	M	MP:0009133	decreased white fat cell size	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0002118	abnormal lipid homeostasis	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0009130	increased white fat cell number	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0004129	abnormal respiratory quotient	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0004082	abnormal habenula morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	11384784
MGI:4453871	M	MP:0005531	increased renal vascular resistance	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	10620200
MGI:4453871	M	MP:0002891	increased insulin sensitivity	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0002842	increased systemic arterial blood pressure	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	12154115
MGI:4453871	M	MP:0008267	abnormal hippocampus CA3 region morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	11384784
MGI:4453871	M	MP:0005526	decreased renal plasma flow rate	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	10620200
MGI:4453871	M	MP:0009643	abnormal urine homeostasis	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	10620200
MGI:4453871	M	MP:0000832	abnormal thalamus morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	11384784
MGI:4453871	M	MP:0004875	increased mean systemic arterial blood pressure	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	12154115
MGI:4453871	M	MP:0005602	decreased angiogenesis	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	14597675
MGI:4453871	M	MP:0008265	abnormal hippocampus CA2 region morphology	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	11384784
MGI:4453871	M	MP:0000230	abnormal systemic arterial blood pressure	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453871	M	MP:0001560	abnormal circulating insulin level	Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd	N	15793237
MGI:4453872	F	MP:0011490	ureteropelvic junction stenosis	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0001745	increased circulating corticosterone level	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	12218346
MGI:4453872	F	MP:0001748	increased circulating adrenocorticotropin level	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	12218346
MGI:4453872	F	MP:0001944	abnormal pancreas morphology	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	19033539
MGI:4453872	F	MP:0011493	double ureter	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0000516	abnormal renal/urinary system morphology	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0003334	pancreas fibrosis	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	19033539
MGI:4453872	F	MP:0003586	dilated ureter	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0003585	large ureter	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0008873	increased physiological sensitivity to xenobiotic	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	19033539
MGI:4453872	F	MP:0002834	decreased heart weight	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4453872	F	MP:0003672	abnormal ureter development	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0011489	ureteropelvic junction atresia	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0001948	vesicoureteral reflux	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0009109	decreased pancreas weight	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	19033539
MGI:4453872	F	MP:0009150	pancreatic acinar cell atrophy	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	19033539
MGI:4453872	F	MP:0000536	hydroureter	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0003446	renal hypoplasia	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0003638	abnormal response/metabolism to endogenous compounds	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4453872	F	MP:0012575	increased noradrenaline level	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	12218346
MGI:4453872	F	MP:0000520	absent kidney	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0003600	ectopic kidney	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0000519	hydronephrosis	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0004875	increased mean systemic arterial blood pressure	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4453872	F	MP:0002135	abnormal kidney morphology	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0011492	ureterovesical junction obstruction	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0003918	decreased kidney weight	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4453872	F	MP:0030761	increased adrenaline level	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	12218346
MGI:4453872	F	MP:0008528	polycystic kidney	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0011415	abnormal aldosterone level	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	12218346
MGI:4453872	F	MP:0000527	abnormal kidney development	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453872	F	MP:0003963	abnormal corticosterone level	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	12218346
MGI:4453872	F	MP:0001629	abnormal heart rate	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4453872	F	MP:0005502	abnormal renal/urinary system physiology	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	10024874
MGI:4453876	F	MP:0006274	abnormal urine sodium level	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd	N	10620200
MGI:4453876	F	MP:0005526	decreased renal plasma flow rate	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd	N	10620200
MGI:4453876	F	MP:0005531	increased renal vascular resistance	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd	N	10620200
MGI:4453876	F	MP:0009643	abnormal urine homeostasis	Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd	N	10620200
MGI:4453877	M	MP:0004486	decreased response of heart to induced stress	Agtr2<tm1Tin>/Y	B6.129P2-Agtr2<tm1Tin>	N	10930448
MGI:4453877	M	MP:0003141	cardiac fibrosis	Agtr2<tm1Tin>/Y	B6.129P2-Agtr2<tm1Tin>	N	12390955
MGI:4453877	M	MP:0000343	abnormal response to cardiac infarction	Agtr2<tm1Tin>/Y	B6.129P2-Agtr2<tm1Tin>	N	12390955
MGI:4453877	M	MP:0003141	cardiac fibrosis	Agtr2<tm1Tin>/Y	B6.129P2-Agtr2<tm1Tin>	N	10930448
MGI:4453877	M	MP:0009763	increased susceptibility to induced morbidity/mortality	Agtr2<tm1Tin>/Y	B6.129P2-Agtr2<tm1Tin>	N	12390955
MGI:4453877	M	MP:0010725	thin interventricular septum	Agtr2<tm1Tin>/Y	B6.129P2-Agtr2<tm1Tin>	N	10930448
MGI:4453877	M	MP:0000278	abnormal myocardial fiber morphology	Agtr2<tm1Tin>/Y	B6.129P2-Agtr2<tm1Tin>	N	10930448
MGI:4453877	M	MP:0003916	decreased heart left ventricle weight	Agtr2<tm1Tin>/Y	B6.129P2-Agtr2<tm1Tin>	N	12390955
MGI:4453877	M	MP:0003921	abnormal heart left ventricle morphology	Agtr2<tm1Tin>/Y	B6.129P2-Agtr2<tm1Tin>	N	12390955
MGI:4453877	M	MP:0014316	decreased heart left ventricle posterior wall thickness	Agtr2<tm1Tin>/Y	B6.129P2-Agtr2<tm1Tin>	N	10930448
MGI:4454268	M	MP:0004502	decreased incidence of tumors by chemical induction	Agtr2<tm1Tin>/Y	SWR.129P2-Agtr2<tm1Tin>	N	16140932
MGI:4454284	F	MP:0000519	hydronephrosis	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454284	F	MP:0001262	decreased body weight	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454284	F	MP:0011086	postnatal lethality, incomplete penetrance	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454284	F	MP:0001629	abnormal heart rate	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454284	F	MP:0003918	decreased kidney weight	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454284	F	MP:0005333	decreased heart rate	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454284	F	MP:0008872	abnormal physiological response to xenobiotic	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454284	F	MP:0000230	abnormal systemic arterial blood pressure	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454284	F	MP:0003638	abnormal response/metabolism to endogenous compounds	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454284	F	MP:0004876	decreased mean systemic arterial blood pressure	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454284	F	MP:0002834	decreased heart weight	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454285	M	MP:0011086	postnatal lethality, incomplete penetrance	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454285	M	MP:0003638	abnormal response/metabolism to endogenous compounds	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454285	M	MP:0000230	abnormal systemic arterial blood pressure	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454285	M	MP:0003918	decreased kidney weight	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454285	M	MP:0004876	decreased mean systemic arterial blood pressure	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454285	M	MP:0008872	abnormal physiological response to xenobiotic	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454285	M	MP:0005333	decreased heart rate	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454285	M	MP:0000519	hydronephrosis	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454285	M	MP:0002834	decreased heart weight	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454285	M	MP:0001629	abnormal heart rate	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454285	M	MP:0001262	decreased body weight	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454287	M	MP:0001262	decreased body weight	Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454287	M	MP:0004875	increased mean systemic arterial blood pressure	Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454287	M	MP:0005325	abnormal renal glomerulus morphology	Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454287	M	MP:0003918	decreased kidney weight	Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454288	F	MP:0001262	decreased body weight	Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454288	F	MP:0004875	increased mean systemic arterial blood pressure	Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454288	F	MP:0003918	decreased kidney weight	Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454288	F	MP:0005325	abnormal renal glomerulus morphology	Agtr1b<tm1Cof>/Agtr1b<tm1Cof>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454289	M	MP:0011501	increased glomerular capsule space	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454289	M	MP:0011363	renal glomerulus atrophy	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454289	M	MP:0002834	decreased heart weight	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454289	M	MP:0001629	abnormal heart rate	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454289	M	MP:0004876	decreased mean systemic arterial blood pressure	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454289	M	MP:0005416	abnormal circulating protein level	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454289	M	MP:0005333	decreased heart rate	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454289	M	MP:0000230	abnormal systemic arterial blood pressure	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454289	M	MP:0003638	abnormal response/metabolism to endogenous compounds	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454289	M	MP:0003918	decreased kidney weight	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454290	F	MP:0002834	decreased heart weight	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454290	F	MP:0005416	abnormal circulating protein level	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454290	F	MP:0011501	increased glomerular capsule space	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454290	F	MP:0000230	abnormal systemic arterial blood pressure	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454290	F	MP:0003638	abnormal response/metabolism to endogenous compounds	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454290	F	MP:0004876	decreased mean systemic arterial blood pressure	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454290	F	MP:0011363	renal glomerulus atrophy	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454290	F	MP:0005333	decreased heart rate	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454290	F	MP:0003918	decreased kidney weight	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454290	F	MP:0001629	abnormal heart rate	Agtr1a<tm1Unc>/Agtr1a<tm1Unc>,Agtr2<tm1Tin>/Agtr2<tm1Tin>	involves: 129P2/OlaHsd * C57BL/6	N	18497303
MGI:4454427	M	MP:0001925	male infertility	Large1<myd-3J>/Large1<myd-3J>	STOCK Large1<myd-3J>/GrsrJ	N	MGI:4454310
MGI:4454541	M	MP:0002675	asthenozoospermia	Slc2a8<tm1.1Asch>/Slc2a8<tm1.1Asch>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18428038
MGI:4454541	M	MP:0004543	abnormal sperm physiology	Slc2a8<tm1.1Asch>/Slc2a8<tm1.1Asch>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18428038
MGI:4454784	M	MP:0001262	decreased body weight	Plp1<jp-msd>/Y	B6C3-Eda<Ta> Plp1<jp-msd>	N	6883111
MGI:4454784	M	MP:0000745	tremors	Plp1<jp-msd>/Y	B6C3-Eda<Ta> Plp1<jp-msd>	N	6883111
MGI:4454784	M	MP:0000921	demyelination	Plp1<jp-msd>/Y	B6C3-Eda<Ta> Plp1<jp-msd>	N	6883111
MGI:4454797	M	MP:0000920	abnormal myelination	Plp1<jp>/Y	B6C3-Eda<Ta> Plp1<jp>	N	6883111
MGI:4454797	M	MP:0002083	premature death	Plp1<jp>/Y	B6C3-Eda<Ta> Plp1<jp>	N	6883111
MGI:4454797	M	MP:0001262	decreased body weight	Plp1<jp>/Y	B6C3-Eda<Ta> Plp1<jp>	N	6883111
MGI:4454797	M	MP:0000745	tremors	Plp1<jp>/Y	B6C3-Eda<Ta> Plp1<jp>	N	6883111
MGI:4454797	M	MP:0000921	demyelination	Plp1<jp>/Y	B6C3-Eda<Ta> Plp1<jp>	N	6883111
MGI:4455022	F	MP:0000067	osteopetrosis	Mitf<Mi>/Mitf<Mi>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6J) or (involves: 129S1/Sv * C57BL/6J)	N	11930005
MGI:4455022	F	MP:0004982	abnormal osteoclast morphology	Mitf<Mi>/Mitf<Mi>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6J) or (involves: 129S1/Sv * C57BL/6J)	N	11930005
MGI:4455022	F	MP:0001297	microphthalmia	Mitf<Mi>/Mitf<Mi>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6J) or (involves: 129S1/Sv * C57BL/6J)	N	11930005
MGI:4455022	F	MP:0005171	absent coat pigmentation	Mitf<Mi>/Mitf<Mi>,Tfe3<tm1Est>/Tfe3<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6J) or (involves: 129S1/Sv * C57BL/6J)	N	11930005
MGI:4455023	F	MP:0001297	microphthalmia	Mitf<Mi-wh>/Mitf<Mi-wh>,Tfe3<tm1Est>/Tfe3<tm1Est>,Tfec<tm1Est>/Tfec<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL * DBA) or (involves: 129S1/Sv * C57BL * C57BL/6J * DBA)	N	11930005
MGI:4455023	F	MP:0005171	absent coat pigmentation	Mitf<Mi-wh>/Mitf<Mi-wh>,Tfe3<tm1Est>/Tfe3<tm1Est>,Tfec<tm1Est>/Tfec<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL * DBA) or (involves: 129S1/Sv * C57BL * C57BL/6J * DBA)	N	11930005
MGI:4455023	F	MP:0000067	osteopetrosis	Mitf<Mi-wh>/Mitf<Mi-wh>,Tfe3<tm1Est>/Tfe3<tm1Est>,Tfec<tm1Est>/Tfec<tm1Est>	either: (involves: 129/Sv * 129S1/Sv * C57BL * DBA) or (involves: 129S1/Sv * C57BL * C57BL/6J * DBA)	N	11930005
MGI:4455029	F	MP:0000067	osteopetrosis	Mitf<mi-ew>/Mitf<mi-ew>,Tfe3<tm1Est>/Tfe3<+>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6Bn * NAW) or (involves: 129S1/Sv * C57BL/6Bn * C57BL/6J * NAW)	N	11930005
MGI:4455029	F	MP:0001297	microphthalmia	Mitf<mi-ew>/Mitf<mi-ew>,Tfe3<tm1Est>/Tfe3<+>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6Bn * NAW) or (involves: 129S1/Sv * C57BL/6Bn * C57BL/6J * NAW)	N	11930005
MGI:4455029	F	MP:0005171	absent coat pigmentation	Mitf<mi-ew>/Mitf<mi-ew>,Tfe3<tm1Est>/Tfe3<+>	either: (involves: 129/Sv * 129S1/Sv * C57BL/6Bn * NAW) or (involves: 129S1/Sv * C57BL/6Bn * C57BL/6J * NAW)	N	11930005
MGI:4455030	F	MP:0002169	no abnormal phenotype detected	Tfe3<tm1Est>/Tfe3<tm1Est>,Tfeb<tm1Est>/Tfeb<+>	either: (involves: 129/Sv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	N	11930005
MGI:4455334	F	MP:0031421	increased superovulation rate	Tg(Ttr-IGF1)1Sykr/0	FVB/N-Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455334	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(Ttr-IGF1)1Sykr/0	FVB/N-Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0013400	abnormal endometrial gland development	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0009011	prolonged diestrus	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0009364	abnormal mature ovarian follicle morphology	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0009018	short estrus	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0002679	abnormal corpus luteum morphology	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0005158	ovary hypoplasia	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0000662	abnormal branching of the mammary ductal tree	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0009096	decreased endometrial gland number	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0001927	abnormal estrous cycle	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0004896	abnormal endometrium morphology	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0009090	myometrium hypoplasia	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0001923	reduced female fertility	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0009014	prolonged proestrus	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0009091	endometrium hypoplasia	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4455335	F	MP:0031421	increased superovulation rate	Igf1<tm1.1Dlr>/Igf1<tm1.1Dlr>,Tg(Ttr-IGF1)1Sykr/0	FVB.Cg-Igf1<tm1.1Dlr> Tg(Ttr-IGF1)1Sykr	N	19497975
MGI:4456087	M	MP:0001925	male infertility	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ	N	28273169
MGI:4456087	F	MP:0001926	female infertility	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ	N	17877786
MGI:4456087	F	MP:0001926	female infertility	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ	N	28273169
MGI:4456087	M	MP:0001925	male infertility	Sirt1<tm1Mcby>/Sirt1<tm1Mcby>	involves: 129S1/Sv * 129X1/SvJ	N	17877786
MGI:4456168	M	MP:0005389	reproductive system phenotype	X/Tp(Y)1Ct<Sxr-a>	involves: CBA * PCT	Y	5156366
MGI:4456206	F	MP:0004834	ovary hemorrhage	Fshr<tm1Hht>/Fshr<+>	involves: 129S7/SvEvBrd	N	20172968
MGI:4456207	F	MP:0004834	ovary hemorrhage	Fshr<tm1Hht>/Fshr<tm1Hht>	involves: 129S7/SvEvBrd	N	20172968
MGI:4456218	F	MP:0001926	female infertility	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456218	F	MP:0004834	ovary hemorrhage	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456218	F	MP:0008871	abnormal ovarian follicle number	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456218	F	MP:0001126	abnormal ovary morphology	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456218	F	MP:0009009	absent estrous cycle	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456218	F	MP:0031019	increased granulosa cell proliferation	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456218	F	MP:0001927	abnormal estrous cycle	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456218	F	MP:0000627	abnormal mammary gland morphology	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456218	F	MP:0001928	abnormal ovulation	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456218	F	MP:0003579	increased ovarian carcinoma incidence	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456218	F	MP:0009013	abnormal proestrus	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456218	F	MP:0009442	increased ovarian teratoma incidence	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456218	F	MP:0009021	absent estrus	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456218	F	MP:0001923	reduced female fertility	Tg(AMH-Fshr*D580H)#Hht/0	involves: FVB/N	N	20172968
MGI:4456219	F	MP:0004834	ovary hemorrhage	Tg(AMH-Fshr*D580Y)#Hht/0	involves: FVB/N	N	20172968
MGI:4456219	F	MP:0009442	increased ovarian teratoma incidence	Tg(AMH-Fshr*D580Y)#Hht/0	involves: FVB/N	N	20172968
MGI:4456220	F	MP:0004834	ovary hemorrhage	Tg(AMH-Fshr)27Hht/0	involves: FVB/N	N	20172968
MGI:4456220	F	MP:0009442	increased ovarian teratoma incidence	Tg(AMH-Fshr)27Hht/0	involves: FVB/N	N	20172968
MGI:4456246	M	MP:0001922	reduced male fertility	Zfp105<Gt(TEA059)Byg>/Zfp105<Gt(TEA059)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20186958
MGI:4456246	M	MP:0001156	abnormal spermatogenesis	Zfp105<Gt(TEA059)Byg>/Zfp105<Gt(TEA059)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	20186958
MGI:4456351	M	MP:0001169	abnormal bulbourethral gland morphology	Gnptab<Gt(OST97730)Lex>/Gnptab<Gt(OST97730)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	17962477
MGI:4456870	M	MP:0002169	no abnormal phenotype detected	Glod5<Gt(111.1G4)Cmhd>/Y	chimera involves: 129S1/Sv * 129X1/SvJ	N	MGI:4456860
MGI:4456873	M	MP:0003400	kinked neural tube	Ccdc160<Gt(179B2)Cmhd>/Y	chimera involves: 129S1/Sv * 129X1/SvJ	N	MGI:4456860
MGI:4456873	M	MP:0000292	distended pericardium	Ccdc160<Gt(179B2)Cmhd>/Y	chimera involves: 129S1/Sv * 129X1/SvJ	N	MGI:4456860
MGI:4456873	M	MP:0000928	incomplete rostral neuropore closure	Ccdc160<Gt(179B2)Cmhd>/Y	chimera involves: 129S1/Sv * 129X1/SvJ	N	MGI:4456860
MGI:4456873	M	MP:0009328	delayed heart looping	Ccdc160<Gt(179B2)Cmhd>/Y	chimera involves: 129S1/Sv * 129X1/SvJ	N	MGI:4456860
MGI:4456873	M	MP:0009657	failure of chorioallantoic fusion	Ccdc160<Gt(179B2)Cmhd>/Y	chimera involves: 129S1/Sv * 129X1/SvJ	N	MGI:4456860
MGI:4456873	M	MP:0002151	abnormal neural tube morphology	Ccdc160<Gt(179B2)Cmhd>/Y	chimera involves: 129S1/Sv * 129X1/SvJ	N	MGI:4456860
MGI:4456873	M	MP:0004073	caudal body truncation	Ccdc160<Gt(179B2)Cmhd>/Y	chimera involves: 129S1/Sv * 129X1/SvJ	N	MGI:4456860
MGI:4456873	M	MP:0000929	open neural tube	Ccdc160<Gt(179B2)Cmhd>/Y	chimera involves: 129S1/Sv * 129X1/SvJ	N	MGI:4456860
MGI:4456884	M	MP:0002084	abnormal developmental patterning	Otud5<Gt(A021B07)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4456884	M	MP:0001700	abnormal embryo turning	Otud5<Gt(A021B07)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4456887	M	MP:0002169	no abnormal phenotype detected	Med14<Gt(A055C04)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4456888	M	MP:0001695	abnormal gastrulation	Bcor<Gt(A20062)Wrst>/Y	chimera involves: 129S1/Sv * 129X1/SvJ	N	MGI:4456860
MGI:4456889	M	MP:0002169	no abnormal phenotype detected	Kif4<Gt(AA0042)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456890	M	MP:0002169	no abnormal phenotype detected	Apool<Gt(AC0470)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456891	M	MP:0002169	no abnormal phenotype detected	Rlim<Gt(AD0035)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456893	M	MP:0003984	embryonic growth retardation	Klf8<Gt(AD0932)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456965	M	MP:0002169	no abnormal phenotype detected	Map7d2<Gt(AF0577)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456966	M	MP:0002169	no abnormal phenotype detected	Syap1<Gt(AF0128)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456967	M	MP:0002151	abnormal neural tube morphology	Zdhhc15<Gt(AH0619)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456967	M	MP:0003984	embryonic growth retardation	Zdhhc15<Gt(AH0619)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456968	M	MP:0002169	no abnormal phenotype detected	Fam120c<Gt(AP0628)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456969	M	MP:0002169	no abnormal phenotype detected	Ctps2<Gt(AS1012)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456970	M	MP:0003984	embryonic growth retardation	Steep1<Gt(AW0613)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456979	M	MP:0003984	embryonic growth retardation	Pir<Gt(AW0646)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456993	M	MP:0002169	no abnormal phenotype detected	Snx12<Gt(AY0032)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456994	M	MP:0002169	no abnormal phenotype detected	Pabir2<Gt(AZ0548)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456995	M	MP:0002169	no abnormal phenotype detected	Vbp1<Gt(BA0243)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4456998	M	MP:0002169	no abnormal phenotype detected	Ogt<Gt(BGA526)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457013	M	MP:0002769	abnormal vas deferens morphology	Porcn<Gt(CSD256)Byg>/Y	chimera involves: 129P2/OlaHsd	N	22412863
MGI:4457013	M	MP:0002085	abnormal embryonic tissue morphology	Porcn<Gt(CSD256)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457032	M	MP:0002169	no abnormal phenotype detected	Pola1<Gt(CSG241)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457056	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Bcor<Gt(DB0053)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457056	M	MP:0000433	microcephaly	Bcor<Gt(DB0053)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457056	M	MP:0004251	failure of heart looping	Bcor<Gt(DB0053)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457056	M	MP:0001689	incomplete somite formation	Bcor<Gt(DB0053)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457056	M	MP:0003232	abnormal forebrain development	Bcor<Gt(DB0053)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457063	M	MP:0001701	incomplete embryo turning	Huwe1<Gt(DC0732)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457063	M	MP:0000433	microcephaly	Huwe1<Gt(DC0732)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457063	M	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Huwe1<Gt(DC0732)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457063	M	MP:0003984	embryonic growth retardation	Huwe1<Gt(DC0732)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457063	M	MP:0002188	small heart	Huwe1<Gt(DC0732)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457083	M	MP:0001695	abnormal gastrulation	Nono<Gt(E086B07)Wrst>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457095	M	MP:0002169	no abnormal phenotype detected	Flna<Gt(F015B06)Wrst>/Y	chimera involves: 129S1/Sv * 129X1/SvJ	N	MGI:4456860
MGI:4457096	M	MP:0002084	abnormal developmental patterning	Cul4b<Gt(M119G06)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4457099	M	MP:0002084	abnormal developmental patterning	Kdm5c<Gt(P026G11)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6	N	MGI:4456860
MGI:4457099	M	MP:0000266	abnormal heart morphology	Kdm5c<Gt(P026G11)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6	N	MGI:4456860
MGI:4457107	M	MP:0002084	abnormal developmental patterning	Atrx<Gt(P034C09)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6	N	MGI:4456860
MGI:4457115	M	MP:0001685	abnormal endoderm development	Huwe1<Gt(P036B01)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6	N	MGI:4456860
MGI:4457121	M	MP:0002169	no abnormal phenotype detected	Bclaf3<Gt(P078F05)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4457123	M	MP:0002084	abnormal developmental patterning	Huwe1<Gt(P125E01)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4457123	M	MP:0001695	abnormal gastrulation	Huwe1<Gt(P125E01)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4457125	M	MP:0002084	abnormal developmental patterning	Rbm3<Gt(PST7787)Mfgc>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4457125	M	MP:0006386	absent somites	Rbm3<Gt(PST7787)Mfgc>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4457128	M	MP:0001700	abnormal embryo turning	Rbbp7<Gt(Q017B06)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6J	N	MGI:4456860
MGI:4457128	M	MP:0002084	abnormal developmental patterning	Rbbp7<Gt(Q017B06)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6J	N	MGI:4456860
MGI:4457139	M	MP:0003984	embryonic growth retardation	Brwd3<Gt(RHA090)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457139	M	MP:0012062	small tail bud	Brwd3<Gt(RHA090)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457139	M	MP:0000433	microcephaly	Brwd3<Gt(RHA090)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457140	M	MP:0003232	abnormal forebrain development	Kdm6a<Gt(RRA094)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457140	M	MP:0000929	open neural tube	Kdm6a<Gt(RRA094)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457140	M	MP:0003400	kinked neural tube	Kdm6a<Gt(RRA094)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457140	M	MP:0000913	abnormal brain development	Kdm6a<Gt(RRA094)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457201	M	MP:0002169	no abnormal phenotype detected	Ftsj1<Gt(RRD143)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457206	M	MP:0002169	no abnormal phenotype detected	Wdr44<Gt(RRE018)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457211	M	MP:0011732	decreased somite size	Akap17b<Gt(RRI131)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457211	M	MP:0002084	abnormal developmental patterning	Akap17b<Gt(RRI131)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457211	M	MP:0009768	impaired somite development	Akap17b<Gt(RRI131)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457211	M	MP:0002085	abnormal embryonic tissue morphology	Akap17b<Gt(RRI131)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457211	M	MP:0005385	cardiovascular system phenotype	Akap17b<Gt(RRI131)Byg>/Y	chimera involves: 129P2/OlaHsd	Y	MGI:4456860
MGI:4457211	M	MP:0003400	kinked neural tube	Akap17b<Gt(RRI131)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457211	M	MP:0000432	abnormal head morphology	Akap17b<Gt(RRI131)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457211	M	MP:0003984	embryonic growth retardation	Akap17b<Gt(RRI131)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457211	M	MP:0001698	decreased embryo size	Akap17b<Gt(RRI131)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457211	M	MP:0009657	failure of chorioallantoic fusion	Akap17b<Gt(RRI131)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457269	M	MP:0002169	no abnormal phenotype detected	Lrch2<Gt(RRI232)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457271	M	MP:0002169	no abnormal phenotype detected	Txlng<Gt(RRJ292)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457274	M	MP:0014052	increased male germ cell apoptosis	Mov10l1<tm1.2Eno>/Mov10l1<tm1.2Eno>	involves: 129S/SvEv * C57BL/6	N	20547853
MGI:4457274	M	MP:0001154	seminiferous tubule degeneration	Mov10l1<tm1.2Eno>/Mov10l1<tm1.2Eno>	involves: 129S/SvEv * C57BL/6	N	20547853
MGI:4457274	M	MP:0001153	small seminiferous tubules	Mov10l1<tm1.2Eno>/Mov10l1<tm1.2Eno>	involves: 129S/SvEv * C57BL/6	N	20547853
MGI:4457274	M	MP:0008261	arrest of male meiosis	Mov10l1<tm1.2Eno>/Mov10l1<tm1.2Eno>	involves: 129S/SvEv * C57BL/6	N	20547853
MGI:4457274	M	MP:0001925	male infertility	Mov10l1<tm1.2Eno>/Mov10l1<tm1.2Eno>	involves: 129S/SvEv * C57BL/6	N	20547853
MGI:4457274	M	MP:0006380	abnormal spermatid morphology	Mov10l1<tm1.2Eno>/Mov10l1<tm1.2Eno>	involves: 129S/SvEv * C57BL/6	N	20547853
MGI:4457274	M	MP:0004852	decreased testis weight	Mov10l1<tm1.2Eno>/Mov10l1<tm1.2Eno>	involves: 129S/SvEv * C57BL/6	N	20547853
MGI:4457274	M	MP:0003698	abnormal male reproductive system physiology	Mov10l1<tm1.2Eno>/Mov10l1<tm1.2Eno>	involves: 129S/SvEv * C57BL/6	N	20547853
MGI:4457274	M	MP:0005159	azoospermia	Mov10l1<tm1.2Eno>/Mov10l1<tm1.2Eno>	involves: 129S/SvEv * C57BL/6	N	20547853
MGI:4457274	M	MP:0005169	abnormal male meiosis	Mov10l1<tm1.2Eno>/Mov10l1<tm1.2Eno>	involves: 129S/SvEv * C57BL/6	N	20547853
MGI:4457274	M	MP:0006379	abnormal spermatocyte morphology	Mov10l1<tm1.2Eno>/Mov10l1<tm1.2Eno>	involves: 129S/SvEv * C57BL/6	N	20547853
MGI:4457277	M	MP:0002169	no abnormal phenotype detected	Enox2<Gt(RRJ357)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457279	M	MP:0002169	no abnormal phenotype detected	Tab3<Gt(RRK351)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457280	M	MP:0002169	no abnormal phenotype detected	Atp11c<Gt(RRM203)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457281	M	MP:0002169	no abnormal phenotype detected	Pdzd4<Gt(RRO278)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457282	M	MP:0004180	failure of initiation of embryo turning	Rps6ka6<Gt(RRS057)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457282	M	MP:0012082	delayed heart development	Rps6ka6<Gt(RRS057)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457282	M	MP:0009331	absent primitive node	Rps6ka6<Gt(RRS057)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457282	M	MP:0000267	abnormal heart development	Rps6ka6<Gt(RRS057)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457282	M	MP:0001695	abnormal gastrulation	Rps6ka6<Gt(RRS057)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457282	M	MP:0000433	microcephaly	Rps6ka6<Gt(RRS057)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457282	M	MP:0002230	abnormal primitive streak formation	Rps6ka6<Gt(RRS057)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457282	M	MP:0009657	failure of chorioallantoic fusion	Rps6ka6<Gt(RRS057)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457282	M	MP:0004073	caudal body truncation	Rps6ka6<Gt(RRS057)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457282	M	MP:0002231	abnormal primitive streak morphology	Rps6ka6<Gt(RRS057)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457286	M	MP:0005159	azoospermia	Mov10l1<tm1.2Jw>/Mov10l1<tm1.2Jw>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	20534472
MGI:4457286	M	MP:0003698	abnormal male reproductive system physiology	Mov10l1<tm1.2Jw>/Mov10l1<tm1.2Jw>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	20534472
MGI:4457286	M	MP:0004852	decreased testis weight	Mov10l1<tm1.2Jw>/Mov10l1<tm1.2Jw>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	20534472
MGI:4457286	M	MP:0001147	small testis	Mov10l1<tm1.2Jw>/Mov10l1<tm1.2Jw>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	20534472
MGI:4457286	M	MP:0001925	male infertility	Mov10l1<tm1.2Jw>/Mov10l1<tm1.2Jw>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	20534472
MGI:4457286	M	MP:0008261	arrest of male meiosis	Mov10l1<tm1.2Jw>/Mov10l1<tm1.2Jw>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	20534472
MGI:4457286	M	MP:0005169	abnormal male meiosis	Mov10l1<tm1.2Jw>/Mov10l1<tm1.2Jw>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	20534472
MGI:4457287	M	MP:0002169	no abnormal phenotype detected	Wnk3<Gt(RRU456)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457288	M	MP:0002169	no abnormal phenotype detected	Taf9b<Gt(TEA124)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457289	M	MP:0002169	no abnormal phenotype detected	Diaph2<Gt(W005C03)Wrst>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457316	M	MP:0002169	no abnormal phenotype detected	Rbm41<Gt(W007A05)Wrst>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457319	M	MP:0002169	no abnormal phenotype detected	Usp9x<Gt(W059E04)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4457320	M	MP:0002169	no abnormal phenotype detected	Bclaf3<Gt(W069B04)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4457322	M	MP:0001695	abnormal gastrulation	Bcor<Gt(W096D07)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4457324	M	MP:0002169	no abnormal phenotype detected	Rab9<Gt(W255D06)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4457325	M	MP:0009781	abnormal preimplantation embryo development	Cox7b<Gt(XH290)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457327	M	MP:0005379	endocrine/exocrine gland phenotype	Ammecr1<Gt(XK571)Byg>/Y	chimera involves: 129P2/OlaHsd	Y	MGI:4456860
MGI:4457328	M	MP:0002169	no abnormal phenotype detected	Chic1<Gt(XQ0221)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457329	M	MP:0002169	no abnormal phenotype detected	Jade3<Gt(XT0269)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457493	F	MP:0001926	female infertility	Por<tm3Ding>/Por<tm3Ding>	C57BL/6-Por<tm3Ding>	N	20375200
MGI:4457494	F	MP:0001926	female infertility	Por<tm3Ding>/Por<tm3Ding>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * DBA	N	20375200
MGI:4457498	F	MP:0008000	increased ovary tumor incidence	Sav1<tm1Dlim>/Sav1<+>	involves: 129S1/Sv * 129X1/SvJ	N	20404163
MGI:4457502	M	MP:0001154	seminiferous tubule degeneration	Zbtb16<lu>/Zbtb16<lu>	involves: C3H/He * C57BL/6	N	20338044
MGI:4457645	M	MP:0002901	increased urine phosphate level	Clcn5<tm2.1Tjj>/Y	involves: 129P2/OlaHsd * 129X1/SvJ * BALB/cJ * C57BL/6	N	20430975
MGI:4457645	M	MP:0001762	polyuria	Clcn5<tm2.1Tjj>/Y	involves: 129P2/OlaHsd * 129X1/SvJ * BALB/cJ * C57BL/6	N	20430975
MGI:4457645	M	MP:0001759	increased urine glucose level	Clcn5<tm2.1Tjj>/Y	involves: 129P2/OlaHsd * 129X1/SvJ * BALB/cJ * C57BL/6	N	20430975
MGI:4457645	M	MP:0002962	increased urine protein level	Clcn5<tm2.1Tjj>/Y	involves: 129P2/OlaHsd * 129X1/SvJ * BALB/cJ * C57BL/6	N	20430975
MGI:4457645	M	MP:0005441	increased urine calcium level	Clcn5<tm2.1Tjj>/Y	involves: 129P2/OlaHsd * 129X1/SvJ * BALB/cJ * C57BL/6	N	20430975
MGI:4457645	M	MP:0011471	decreased urine creatinine level	Clcn5<tm2.1Tjj>/Y	involves: 129P2/OlaHsd * 129X1/SvJ * BALB/cJ * C57BL/6	N	20430975
MGI:4457645	M	MP:0011559	increased urine insulin level	Clcn5<tm2.1Tjj>/Y	involves: 129P2/OlaHsd * 129X1/SvJ * BALB/cJ * C57BL/6	N	20430975
MGI:4457645	M	MP:0005621	abnormal cell physiology	Clcn5<tm2.1Tjj>/Y	involves: 129P2/OlaHsd * 129X1/SvJ * BALB/cJ * C57BL/6	N	20430975
MGI:4457645	M	MP:0009350	decreased urine pH	Clcn5<tm2.1Tjj>/Y	involves: 129P2/OlaHsd * 129X1/SvJ * BALB/cJ * C57BL/6	N	20430975
MGI:4457646	M	MP:0005384	cellular phenotype	Clcn5<tm3.1Tjj>/Y	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6	Y	20430975
MGI:4457647	M	MP:0011559	increased urine insulin level	Clcn5<tm1Tjj>/Y	involves: 129	N	20430975
MGI:4457647	M	MP:0001759	increased urine glucose level	Clcn5<tm1Tjj>/Y	involves: 129	N	20430975
MGI:4457647	M	MP:0009350	decreased urine pH	Clcn5<tm1Tjj>/Y	involves: 129	N	20430975
MGI:4457647	M	MP:0005621	abnormal cell physiology	Clcn5<tm1Tjj>/Y	involves: 129	N	20430975
MGI:4457647	M	MP:0005441	increased urine calcium level	Clcn5<tm1Tjj>/Y	involves: 129	N	20430975
MGI:4457647	M	MP:0002901	increased urine phosphate level	Clcn5<tm1Tjj>/Y	involves: 129	N	20430975
MGI:4457731	M	MP:0001932	abnormal spermiogenesis	Boll<tm1Eyx>/Boll<tm1Eyx>	involves: 129 * C57BL/6	N	20335278
MGI:4457731	M	MP:0001147	small testis	Boll<tm1Eyx>/Boll<tm1Eyx>	involves: 129 * C57BL/6	N	20335278
MGI:4457731	M	MP:0001156	abnormal spermatogenesis	Boll<tm1Eyx>/Boll<tm1Eyx>	involves: 129 * C57BL/6	N	20335278
MGI:4457731	M	MP:0008279	arrest of spermiogenesis	Boll<tm1Eyx>/Boll<tm1Eyx>	involves: 129 * C57BL/6	N	20335278
MGI:4457731	M	MP:0001155	arrest of spermatogenesis	Boll<tm1Eyx>/Boll<tm1Eyx>	involves: 129 * C57BL/6	N	20335278
MGI:4457731	M	MP:0004852	decreased testis weight	Boll<tm1Eyx>/Boll<tm1Eyx>	involves: 129 * C57BL/6	N	20335278
MGI:4457731	M	MP:0020550	multinucleated giant male germ cells	Boll<tm1Eyx>/Boll<tm1Eyx>	involves: 129 * C57BL/6	N	20335278
MGI:4457731	M	MP:0005159	azoospermia	Boll<tm1Eyx>/Boll<tm1Eyx>	involves: 129 * C57BL/6	N	20335278
MGI:4457731	M	MP:0008280	abnormal male germ cell apoptosis	Boll<tm1Eyx>/Boll<tm1Eyx>	involves: 129 * C57BL/6	N	20335278
MGI:4457731	M	MP:0001925	male infertility	Boll<tm1Eyx>/Boll<tm1Eyx>	involves: 129 * C57BL/6	N	20335278
MGI:4457861	M	MP:0001698	decreased embryo size	Usp9x<Gt(XK141)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457861	M	MP:0009657	failure of chorioallantoic fusion	Usp9x<Gt(XK141)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457861	M	MP:0000929	open neural tube	Usp9x<Gt(XK141)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457861	M	MP:0004251	failure of heart looping	Usp9x<Gt(XK141)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457861	M	MP:0012105	delayed gastrulation	Usp9x<Gt(XK141)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457861	M	MP:0004180	failure of initiation of embryo turning	Usp9x<Gt(XK141)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457868	M	MP:0002169	no abnormal phenotype detected	Nono<Gt(E089G04)Wrst>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457869	M	MP:0001695	abnormal gastrulation	Nono<Gt(P030B07)Wrst>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457872	M	MP:0008762	embryonic lethality	Alg13<Gt(P035H04)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6J	N	MGI:4456860
MGI:4457872	M	MP:0002084	abnormal developmental patterning	Alg13<Gt(P035H04)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6J	N	MGI:4456860
MGI:4457872	M	MP:0004187	cardia bifida	Alg13<Gt(P035H04)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6J	N	MGI:4456860
MGI:4457872	M	MP:0004180	failure of initiation of embryo turning	Alg13<Gt(P035H04)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6J	N	MGI:4456860
MGI:4457873	M	MP:0001696	failure to gastrulate	Alg13<Gt(P088H08)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4457884	M	MP:0002084	abnormal developmental patterning	Bcor<Gt(P101H07)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4457884	M	MP:0001700	abnormal embryo turning	Bcor<Gt(P101H07)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4457886	M	MP:0001689	incomplete somite formation	Bcor<Gt(XE541)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457886	M	MP:0000433	microcephaly	Bcor<Gt(XE541)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457886	M	MP:0003232	abnormal forebrain development	Bcor<Gt(XE541)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4457886	M	MP:0000269	abnormal heart looping	Bcor<Gt(XE541)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4458093	F	MP:0004021	abnormal rod electrophysiology	Rpgr<tm1Wbrg>/Rpgr<tm1Wbrg>	B6.129P2-Rpgr<tm1Wbrg>	N	20007830
MGI:4458093	F	MP:0003730	abnormal photoreceptor inner segment morphology	Rpgr<tm1Wbrg>/Rpgr<tm1Wbrg>	B6.129P2-Rpgr<tm1Wbrg>	N	20007830
MGI:4458093	F	MP:0003729	abnormal photoreceptor outer segment morphology	Rpgr<tm1Wbrg>/Rpgr<tm1Wbrg>	B6.129P2-Rpgr<tm1Wbrg>	N	20007830
MGI:4458093	F	MP:0004022	abnormal cone electrophysiology	Rpgr<tm1Wbrg>/Rpgr<tm1Wbrg>	B6.129P2-Rpgr<tm1Wbrg>	N	20007830
MGI:4458093	F	MP:0008515	thin retina outer nuclear layer	Rpgr<tm1Wbrg>/Rpgr<tm1Wbrg>	B6.129P2-Rpgr<tm1Wbrg>	N	20007830
MGI:4458094	F	MP:0005391	vision/eye phenotype	Rpgr<tm1Wbrg>/Rpgr<tm1Wbrg>	C.129P2-Rpgr<tm1Wbrg>	Y	20007830
MGI:4458094	F	MP:0004022	abnormal cone electrophysiology	Rpgr<tm1Wbrg>/Rpgr<tm1Wbrg>	C.129P2-Rpgr<tm1Wbrg>	N	20007830
MGI:4458094	F	MP:0004021	abnormal rod electrophysiology	Rpgr<tm1Wbrg>/Rpgr<tm1Wbrg>	C.129P2-Rpgr<tm1Wbrg>	N	20007830
MGI:4458094	F	MP:0008446	decreased retina cone cell number	Rpgr<tm1Wbrg>/Rpgr<tm1Wbrg>	C.129P2-Rpgr<tm1Wbrg>	N	20007830
MGI:4458095	F	MP:0005253	abnormal eye physiology	Rpe65<450M>/Rpe65<450M>,Rpgr<tm1Wbrg>/Rpgr<tm1Wbrg>	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	20007830
MGI:4458095	F	MP:0002092	abnormal eye morphology	Rpe65<450M>/Rpe65<450M>,Rpgr<tm1Wbrg>/Rpgr<tm1Wbrg>	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	20007830
MGI:4458099	M	MP:0001925	male infertility	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458099	M	MP:0009851	abnormal Sertoli cell phagocytosis	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458099	M	MP:0005169	abnormal male meiosis	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458099	M	MP:0014052	increased male germ cell apoptosis	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458099	M	MP:0008898	abnormal acrosome morphology	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458099	M	MP:0008279	arrest of spermiogenesis	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458099	M	MP:0004852	decreased testis weight	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458099	M	MP:0006378	abnormal spermatogonia morphology	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458099	M	MP:0006380	abnormal spermatid morphology	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458099	M	MP:0005159	azoospermia	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458099	M	MP:0004182	abnormal spermiation	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458099	M	MP:0001156	abnormal spermatogenesis	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458099	M	MP:0006379	abnormal spermatocyte morphology	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458099	M	MP:0001154	seminiferous tubule degeneration	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	20359371
MGI:4458100	M	MP:0004852	decreased testis weight	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	FVB.Cg-Ehd1<tm1.2Haba>	N	20359371
MGI:4458100	M	MP:0001925	male infertility	Ehd1<tm1.2Haba>/Ehd1<tm1.2Haba>	FVB.Cg-Ehd1<tm1.2Haba>	N	20359371
MGI:4458342	M	MP:0001922	reduced male fertility	Agtpbp1<pcd-2J>/Agtpbp1<pcd-2J>	involves: SM/J	N	11884758
MGI:4458360	M	MP:0002169	no abnormal phenotype detected	Hdx<Gt(CD0231)Wtsi>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4458361	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Atrx<Gt(E085A04)Wrst>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4458361	M	MP:0002084	abnormal developmental patterning	Atrx<Gt(E085A04)Wrst>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4458363	M	MP:0012132	abnormal midbrain-hindbrain boundary morphology	Steep1<Gt(RRG250)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4458363	M	MP:0012138	decreased forebrain size	Steep1<Gt(RRG250)Byg>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4458380	M	MP:0002084	abnormal developmental patterning	Atrx<Gt(P034D09)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6J	N	MGI:4456860
MGI:4458380	M	MP:0000266	abnormal heart morphology	Atrx<Gt(P034D09)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6J	N	MGI:4456860
MGI:4458413	M	MP:0002769	abnormal vas deferens morphology	Dact1<tm1Yegc>/Dact1<tm1Yegc>	B6.129-Dact1<tm1Yegc>	N	20145239
MGI:4458413	F	MP:0001926	female infertility	Dact1<tm1Yegc>/Dact1<tm1Yegc>	B6.129-Dact1<tm1Yegc>	N	20145239
MGI:4458413	F	MP:0009084	blind uterus	Dact1<tm1Yegc>/Dact1<tm1Yegc>	B6.129-Dact1<tm1Yegc>	N	20145239
MGI:4458413	F	MP:0003535	absent vagina	Dact1<tm1Yegc>/Dact1<tm1Yegc>	B6.129-Dact1<tm1Yegc>	N	20145239
MGI:4458413	M	MP:0009204	absent external male genitalia	Dact1<tm1Yegc>/Dact1<tm1Yegc>	B6.129-Dact1<tm1Yegc>	N	20145239
MGI:4458413	F	MP:0009709	hydrometra	Dact1<tm1Yegc>/Dact1<tm1Yegc>	B6.129-Dact1<tm1Yegc>	N	20145239
MGI:4458413	F	MP:0009211	absent external female genitalia	Dact1<tm1Yegc>/Dact1<tm1Yegc>	B6.129-Dact1<tm1Yegc>	N	20145239
MGI:4459015	M	MP:0004073	caudal body truncation	Dlg3<Gt(P038A02)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6J	N	MGI:4456860
MGI:4459015	M	MP:0003232	abnormal forebrain development	Dlg3<Gt(P038A02)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6J	N	MGI:4456860
MGI:4459015	M	MP:0004180	failure of initiation of embryo turning	Dlg3<Gt(P038A02)Wrst>/Y	chimera involves: 129S6/SvEvTac * C57BL/6J	N	MGI:4456860
MGI:4459017	M	MP:0001914	hemorrhage	Diaph2<Gt(E093H03)Wrst>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4459017	M	MP:0002152	abnormal brain morphology	Diaph2<Gt(E093H03)Wrst>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4459017	M	MP:0000266	abnormal heart morphology	Diaph2<Gt(E093H03)Wrst>/Y	chimera involves: 129P2/OlaHsd	N	MGI:4456860
MGI:4459132	M	MP:0002169	no abnormal phenotype detected	Rbm10<Gt(W081D04)Wrst>/Y	chimera involves: 129S2/SvPas	N	MGI:4456860
MGI:4459311	M	MP:0003048	abnormal cervical vertebrae morphology	Ripply1<tm1.1Sjt>/Y	involves: 129S1/Sv * FVB/N	N	20346937
MGI:4459312	F	MP:0003048	abnormal cervical vertebrae morphology	Ripply1<tm1.1Sjt>/Ripply1<tm1.1Sjt>	involves: 129S1/Sv * FVB/N	N	20346937
MGI:4459313	F	MP:0000137	abnormal vertebrae morphology	Ripply1<tm1.1Sjt>/Ripply1<tm1.1Sjt>,Ripply2<tm1.1Ysa>/Ripply2<tm1.1Ysa>	involves: 129S1/Sv * C57BL/6 * CBA * FVB/N	N	20346937
MGI:4459313	F	MP:0008530	abnormal rostral-caudal patterning of the somites	Ripply1<tm1.1Sjt>/Ripply1<tm1.1Sjt>,Ripply2<tm1.1Ysa>/Ripply2<tm1.1Ysa>	involves: 129S1/Sv * C57BL/6 * CBA * FVB/N	N	20346937
MGI:4459313	F	MP:0000140	absent vertebral pedicles	Ripply1<tm1.1Sjt>/Ripply1<tm1.1Sjt>,Ripply2<tm1.1Ysa>/Ripply2<tm1.1Ysa>	involves: 129S1/Sv * C57BL/6 * CBA * FVB/N	N	20346937
MGI:4459314	M	MP:0000137	abnormal vertebrae morphology	Ripply1<tm1.1Sjt>/Y,Ripply2<tm1.1Ysa>/Ripply2<tm1.1Ysa>	involves: 129S1/Sv * C57BL/6 * CBA * FVB/N	N	20346937
MGI:4459314	M	MP:0008530	abnormal rostral-caudal patterning of the somites	Ripply1<tm1.1Sjt>/Y,Ripply2<tm1.1Ysa>/Ripply2<tm1.1Ysa>	involves: 129S1/Sv * C57BL/6 * CBA * FVB/N	N	20346937
MGI:4459314	M	MP:0000140	absent vertebral pedicles	Ripply1<tm1.1Sjt>/Y,Ripply2<tm1.1Ysa>/Ripply2<tm1.1Ysa>	involves: 129S1/Sv * C57BL/6 * CBA * FVB/N	N	20346937
MGI:4459316	F	MP:0000662	abnormal branching of the mammary ductal tree	Esr1<tm1Sakh>/Esr1<tm1Sakh>,Tg(MMTV-cre)4Mam/?	involves: 129P2/OlaHsd * C57BL/6 * FVB	N	17785410
MGI:4459317	F	MP:0009506	abnormal mammary gland alveolus morphology	Esr1<tm1Sakh>/Esr1<tm1Sakh>,Tg(Wap-cre)11738Mam/?	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17785410
MGI:4459317	F	MP:0000627	abnormal mammary gland morphology	Esr1<tm1Sakh>/Esr1<tm1Sakh>,Tg(Wap-cre)11738Mam/?	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17785410
MGI:4459317	F	MP:0000662	abnormal branching of the mammary ductal tree	Esr1<tm1Sakh>/Esr1<tm1Sakh>,Tg(Wap-cre)11738Mam/?	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17785410
MGI:4459317	F	MP:0001882	abnormal lactation	Esr1<tm1Sakh>/Esr1<tm1Sakh>,Tg(Wap-cre)11738Mam/?	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	17785410
MGI:4459433	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Rnf8<Gt(AS0574)Wtsi>/Rnf8<Gt(AS0574)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:4459433	M	MP:0001922	reduced male fertility	Rnf8<Gt(AS0574)Wtsi>/Rnf8<Gt(AS0574)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:4459433	M	MP:0006379	abnormal spermatocyte morphology	Rnf8<Gt(AS0574)Wtsi>/Rnf8<Gt(AS0574)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:4459433	M	MP:0005159	azoospermia	Rnf8<Gt(AS0574)Wtsi>/Rnf8<Gt(AS0574)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:4459433	M	MP:0002687	oligozoospermia	Rnf8<Gt(AS0574)Wtsi>/Rnf8<Gt(AS0574)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:4459433	M	MP:0001147	small testis	Rnf8<Gt(AS0574)Wtsi>/Rnf8<Gt(AS0574)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:4459433	M	MP:0001154	seminiferous tubule degeneration	Rnf8<Gt(AS0574)Wtsi>/Rnf8<Gt(AS0574)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:4459433	M	MP:0001156	abnormal spermatogenesis	Rnf8<Gt(AS0574)Wtsi>/Rnf8<Gt(AS0574)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:4459433	M	MP:0006378	abnormal spermatogonia morphology	Rnf8<Gt(AS0574)Wtsi>/Rnf8<Gt(AS0574)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20385750
MGI:4459458	M	MP:0005287	narrow eye opening	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0001199	thin skin	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0002233	abnormal nose morphology	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0000585	kinked tail	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0006365	absent guard hair	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0006366	absent zigzag hairs	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0006371	absent hair follicle pheomelanosome pheomelanin	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0002237	abnormal nasal cavity morphology	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0003704	abnormal hair follicle development	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0009003	abnormal vibrissa number	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0002095	abnormal skin pigmentation	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0013580	abnormal nasal gland morphology	Eda<Ta>/Y	Not Specified	N	27590203
MGI:4459458	M	MP:0013582	abnormal lateral nasal gland morphology	Eda<Ta>/Y	Not Specified	N	27590203
MGI:4459458	M	MP:0012078	abnormal tail ring morphology	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0010233	hairless tail	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0002073	abnormal hair growth	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0002074	abnormal hair texture	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459458	M	MP:0000367	abnormal coat/ hair morphology	Eda<Ta>/Y	Not Specified	N	13103353
MGI:4459465	F	MP:0010231	transverse fur striping	Eda<Ta>/Eda<+>	Not Specified	N	13103353
MGI:4459465	F	MP:0006366	absent zigzag hairs	Eda<Ta>/Eda<+>	Not Specified	N	13103353
MGI:4459465	F	MP:0000372	irregular coat pigmentation	Eda<Ta>/Eda<+>	Not Specified	N	13103353
MGI:4459465	F	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta>/Eda<+>	Not Specified	N	13103353
MGI:4459465	F	MP:0006371	absent hair follicle pheomelanosome pheomelanin	Eda<Ta>/Eda<+>	Not Specified	N	13103353
MGI:4459465	F	MP:0009659	striated fur	Eda<Ta>/Eda<+>	Not Specified	N	13103353
MGI:4459465	F	MP:0002074	abnormal hair texture	Eda<Ta>/Eda<+>	Not Specified	N	13103353
MGI:4459465	F	MP:0008538	decreased zigzag hair amount	Eda<Ta>/Eda<+>	Not Specified	N	13103353
MGI:4459466	F	MP:0001923	reduced female fertility	Lmna<Dhe>/Lmna<+>	B6(D2)-Lmna<Dhe>/TyGrsrJ	N	20376364
MGI:4459476	F	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta-9J>/Eda<+>	involves: CBA/J	N	MGI:2384334
MGI:4459476	F	MP:0009659	striated fur	Eda<Ta-9J>/Eda<+>	involves: CBA/J	N	MGI:2384334
MGI:4459476	F	MP:0010231	transverse fur striping	Eda<Ta-9J>/Eda<+>	involves: CBA/J	N	MGI:2384334
MGI:4459476	F	MP:0000372	irregular coat pigmentation	Eda<Ta-9J>/Eda<+>	involves: CBA/J	N	MGI:2384334
MGI:4459477	M	MP:0002111	abnormal tail morphology	Eda<Ta-9J>/Y	involves: CBA/J	N	MGI:2384334
MGI:4459477	M	MP:0005287	narrow eye opening	Eda<Ta-9J>/Y	involves: CBA/J	N	MGI:2384334
MGI:4459477	M	MP:0000367	abnormal coat/ hair morphology	Eda<Ta-9J>/Y	involves: CBA/J	N	MGI:2384334
MGI:4459477	M	MP:0002073	abnormal hair growth	Eda<Ta-9J>/Y	involves: CBA/J	N	MGI:2384334
MGI:4459477	M	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta-9J>/Y	involves: CBA/J	N	MGI:2384334
MGI:4459477	M	MP:0000585	kinked tail	Eda<Ta-9J>/Y	involves: CBA/J	N	MGI:2384334
MGI:4459477	M	MP:0010233	hairless tail	Eda<Ta-9J>/Y	involves: CBA/J	N	MGI:2384334
MGI:4459498	F	MP:0000367	abnormal coat/ hair morphology	Eda<Ta-9J>/Eda<Ta-9J>	involves: CBA/J	N	MGI:2384334
MGI:4459498	F	MP:0002111	abnormal tail morphology	Eda<Ta-9J>/Eda<Ta-9J>	involves: CBA/J	N	MGI:2384334
MGI:4459498	F	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta-9J>/Eda<Ta-9J>	involves: CBA/J	N	MGI:2384334
MGI:4459498	F	MP:0005287	narrow eye opening	Eda<Ta-9J>/Eda<Ta-9J>	involves: CBA/J	N	MGI:2384334
MGI:4459498	F	MP:0002073	abnormal hair growth	Eda<Ta-9J>/Eda<Ta-9J>	involves: CBA/J	N	MGI:2384334
MGI:4459498	F	MP:0000585	kinked tail	Eda<Ta-9J>/Eda<Ta-9J>	involves: CBA/J	N	MGI:2384334
MGI:4459498	F	MP:0010233	hairless tail	Eda<Ta-9J>/Eda<Ta-9J>	involves: CBA/J	N	MGI:2384334
MGI:4459501	M	MP:0010233	hairless tail	Eda<Ta-10J>/Y	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459501	M	MP:0002111	abnormal tail morphology	Eda<Ta-10J>/Y	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459501	M	MP:0000585	kinked tail	Eda<Ta-10J>/Y	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459501	M	MP:0002073	abnormal hair growth	Eda<Ta-10J>/Y	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459501	M	MP:0005287	narrow eye opening	Eda<Ta-10J>/Y	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459501	M	MP:0000367	abnormal coat/ hair morphology	Eda<Ta-10J>/Y	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459501	M	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta-10J>/Y	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459502	F	MP:0000585	kinked tail	Eda<Ta-10J>/Eda<Ta-10J>	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459502	F	MP:0005287	narrow eye opening	Eda<Ta-10J>/Eda<Ta-10J>	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459502	F	MP:0002073	abnormal hair growth	Eda<Ta-10J>/Eda<Ta-10J>	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459502	F	MP:0010233	hairless tail	Eda<Ta-10J>/Eda<Ta-10J>	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459502	F	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta-10J>/Eda<Ta-10J>	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459502	F	MP:0000367	abnormal coat/ hair morphology	Eda<Ta-10J>/Eda<Ta-10J>	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459502	F	MP:0002111	abnormal tail morphology	Eda<Ta-10J>/Eda<Ta-10J>	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459504	F	MP:0010231	transverse fur striping	Eda<Ta-10J>/Eda<+>	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459504	F	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta-10J>/Eda<+>	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459504	F	MP:0000372	irregular coat pigmentation	Eda<Ta-10J>/Eda<+>	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459504	F	MP:0009659	striated fur	Eda<Ta-10J>/Eda<+>	involves: C3H/HeSnJ	N	MGI:65389
MGI:4459533	F	MP:0008687	increased interleukin-2 secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: C57BL/6	N	20493730
MGI:4459533	F	MP:0005348	increased T cell proliferation	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: C57BL/6	N	20493730
MGI:4459533	F	MP:0004762	increased anti-double stranded DNA antibody level	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: C57BL/6	N	20493730
MGI:4459533	F	MP:0008681	increased interleukin-17 secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: C57BL/6	N	20493730
MGI:4459533	F	MP:0008566	increased interferon-gamma secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: C57BL/6	N	20493730
MGI:4459535	F	MP:0008566	increased interferon-gamma secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>,Tg(TcraTcrb)425Cbn/0	involves: 129 * BALB/c * C57BL/6	N	20493730
MGI:4459535	F	MP:0008687	increased interleukin-2 secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>,Tg(TcraTcrb)425Cbn/0	involves: 129 * BALB/c * C57BL/6	N	20493730
MGI:4459535	F	MP:0009336	increased splenocyte proliferation	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>,Tg(TcraTcrb)425Cbn/0	involves: 129 * BALB/c * C57BL/6	N	20493730
MGI:4459535	F	MP:0005000	abnormal immune tolerance	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>,Tg(TcraTcrb)425Cbn/0	involves: 129 * BALB/c * C57BL/6	N	20493730
MGI:4459536	F	MP:0004946	abnormal regulatory T cell physiology	Foxp3<tm2Ayr>/Foxp3<+>,Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	20493730
MGI:4459537	F	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis	Rnf128<tm1Cdon>/Rnf128<+>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0008568	abnormal interleukin secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0009336	increased splenocyte proliferation	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0006082	CNS inflammation	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0008703	decreased interleukin-5 secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0004762	increased anti-double stranded DNA antibody level	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0008700	decreased interleukin-4 secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0008699	increased interleukin-4 secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0008687	increased interleukin-2 secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0005000	abnormal immune tolerance	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0008681	increased interleukin-17 secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0004946	abnormal regulatory T cell physiology	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0008673	decreased interleukin-13 secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0008499	increased IgG1 level	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0001861	lung inflammation	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0002494	increased IgM level	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0008566	increased interferon-gamma secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0009057	increased interleukin-21 secretion	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0008466	enlarged mesenteric lymph nodes	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459538	F	MP:0000691	enlarged spleen	Rnf128<tm1Cdon>/Rnf128<tm1Cdon>	involves: 129 * C57BL/6	N	20493730
MGI:4459540	F	MP:0000562	polydactyly	Ar<Tfm>/Ar<+>,Eda<Ta-25H>/Eda<+>	involves: 101/H * C3H/HeH	N	2055107
MGI:4459540	F	MP:0010231	transverse fur striping	Ar<Tfm>/Ar<+>,Eda<Ta-25H>/Eda<+>	involves: 101/H * C3H/HeH	N	2055107
MGI:4459540	F	MP:0000564	syndactyly	Ar<Tfm>/Ar<+>,Eda<Ta-25H>/Eda<+>	involves: 101/H * C3H/HeH	N	2055107
MGI:4459540	F	MP:0002075	abnormal coat/hair pigmentation	Ar<Tfm>/Ar<+>,Eda<Ta-25H>/Eda<+>	involves: 101/H * C3H/HeH	N	2055107
MGI:4459540	F	MP:0000914	exencephaly	Ar<Tfm>/Ar<+>,Eda<Ta-25H>/Eda<+>	involves: 101/H * C3H/HeH	N	2055107
MGI:4459540	F	MP:0011088	neonatal lethality, incomplete penetrance	Ar<Tfm>/Ar<+>,Eda<Ta-25H>/Eda<+>	involves: 101/H * C3H/HeH	N	2055107
MGI:4459540	F	MP:0009659	striated fur	Ar<Tfm>/Ar<+>,Eda<Ta-25H>/Eda<+>	involves: 101/H * C3H/HeH	N	2055107
MGI:4459540	F	MP:0006369	supernumerary incisors	Ar<Tfm>/Ar<+>,Eda<Ta-25H>/Eda<+>	involves: 101/H * C3H/HeH	N	2055107
MGI:4459540	F	MP:0001265	decreased body size	Ar<Tfm>/Ar<+>,Eda<Ta-25H>/Eda<+>	involves: 101/H * C3H/HeH	N	2055107
MGI:4459540	F	MP:0000372	irregular coat pigmentation	Ar<Tfm>/Ar<+>,Eda<Ta-25H>/Eda<+>	involves: 101/H * C3H/HeH	N	2055107
MGI:4459540	F	MP:0010031	abnormal cranium size	Ar<Tfm>/Ar<+>,Eda<Ta-25H>/Eda<+>	involves: 101/H * C3H/HeH	N	2055107
MGI:4459540	F	MP:0011101	prenatal lethality, incomplete penetrance	Ar<Tfm>/Ar<+>,Eda<Ta-25H>/Eda<+>	involves: 101/H * C3H/HeH	N	2055107
MGI:4459540	F	MP:0000440	domed cranium	Ar<Tfm>/Ar<+>,Eda<Ta-25H>/Eda<+>	involves: 101/H * C3H/HeH	N	2055107
MGI:4459547	F	MP:0011085	postnatal lethality, complete penetrance	C1galt1c1<tm1.2Rdcu>/C1galt1c1<+>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	20439703
MGI:4459547	F	MP:0001914	hemorrhage	C1galt1c1<tm1.2Rdcu>/C1galt1c1<+>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	20439703
MGI:4459547	F	MP:0001732	postnatal growth retardation	C1galt1c1<tm1.2Rdcu>/C1galt1c1<+>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	20439703
MGI:4459547	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	C1galt1c1<tm1.2Rdcu>/C1galt1c1<+>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	20439703
MGI:4459547	F	MP:0001614	abnormal blood vessel morphology	C1galt1c1<tm1.2Rdcu>/C1galt1c1<+>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	20439703
MGI:4459548	M	MP:0003984	embryonic growth retardation	C1galt1c1<tm1.2Rdcu>/Y	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	20439703
MGI:4459548	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	C1galt1c1<tm1.2Rdcu>/Y	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	20439703
MGI:4459548	M	MP:0006054	spinal hemorrhage	C1galt1c1<tm1.2Rdcu>/Y	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	20439703
MGI:4459548	M	MP:0001634	internal hemorrhage	C1galt1c1<tm1.2Rdcu>/Y	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	20439703
MGI:4459815	F	MP:0003313	abnormal locomotor activation	Pcsk1n<tm1Jep>/Pcsk1n<tm1Jep>	Not Specified	N	20367757
MGI:4459815	F	MP:0002757	decreased vertical activity	Pcsk1n<tm1Jep>/Pcsk1n<tm1Jep>	Not Specified	N	20367757
MGI:4459815	F	MP:0001364	decreased anxiety-related response	Pcsk1n<tm1Jep>/Pcsk1n<tm1Jep>	Not Specified	N	20367757
MGI:4459815	F	MP:0003908	decreased stereotypic behavior	Pcsk1n<tm1Jep>/Pcsk1n<tm1Jep>	Not Specified	N	20367757
MGI:4459815	F	MP:0001262	decreased body weight	Pcsk1n<tm1Jep>/Pcsk1n<tm1Jep>	Not Specified	N	20367757
MGI:4459943	M	MP:0002169	no abnormal phenotype detected	Kdm5c<Gt(E008C01)Wrst>/Y	Not Specified	N	MGI:4456860
MGI:4461040	F	MP:0005370	liver/biliary system phenotype	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: FVB/N	Y	20478530
MGI:4461040	F	MP:0005343	increased circulating aspartate transaminase level	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: FVB/N	N	20478530
MGI:4461040	F	MP:0011009	increased circulating glutamate dehydrogenase level	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: FVB/N	N	20478530
MGI:4461040	F	MP:0005376	homeostasis/metabolism phenotype	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: FVB/N	Y	20478530
MGI:4461040	F	MP:0003893	increased hepatocyte proliferation	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: FVB/N	N	20478530
MGI:4461040	F	MP:0003331	increased hepatocellular carcinoma incidence	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: FVB/N	N	20478530
MGI:4461040	F	MP:0000598	abnormal liver morphology	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: FVB/N	N	20478530
MGI:4461040	F	MP:0003333	liver fibrosis	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: FVB/N	N	20478530
MGI:4461040	F	MP:0003887	increased hepatocyte apoptosis	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: FVB/N	N	20478530
MGI:4461040	F	MP:0002941	increased circulating alanine transaminase level	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: FVB/N	N	20478530
MGI:4461041	F	MP:0005376	homeostasis/metabolism phenotype	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Map3k7<tm1Aki>/Map3k7<tm1Aki>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * FVB/N	Y	20478530
MGI:4461041	F	MP:0002941	increased circulating alanine transaminase level	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Map3k7<tm1Aki>/Map3k7<tm1Aki>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * FVB/N	N	20478530
MGI:4461041	F	MP:0010768	mortality/aging	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Map3k7<tm1Aki>/Map3k7<tm1Aki>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * FVB/N	Y	20478530
MGI:4461041	F	MP:0005343	increased circulating aspartate transaminase level	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Map3k7<tm1Aki>/Map3k7<tm1Aki>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * FVB/N	N	20478530
MGI:4461041	F	MP:0003893	increased hepatocyte proliferation	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Map3k7<tm1Aki>/Map3k7<tm1Aki>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * FVB/N	N	20478530
MGI:4461041	F	MP:0005370	liver/biliary system phenotype	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Map3k7<tm1Aki>/Map3k7<tm1Aki>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * FVB/N	Y	20478530
MGI:4461041	F	MP:0003887	increased hepatocyte apoptosis	Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Map3k7<tm1Aki>/Map3k7<tm1Aki>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * FVB/N	N	20478530
MGI:4461047	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<Mo-9J>/Y	involves: C57BL/6J	N	MGI:1329192
MGI:4461051	F	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-9J>/Atp7a<+>	involves: C57BL/6J	N	MGI:1329192
MGI:4461051	F	MP:0001274	curly vibrissae	Atp7a<Mo-9J>/Atp7a<+>	involves: C57BL/6J	N	MGI:1329192
MGI:4461051	F	MP:0000421	mottled coat	Atp7a<Mo-9J>/Atp7a<+>	involves: C57BL/6J	N	MGI:1329192
MGI:4461175	M	MP:0004543	abnormal sperm physiology	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0002660	abnormal caput epididymis morphology	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0014468	disorganized sperm mitochondrial sheath	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0001922	reduced male fertility	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0009238	coiled sperm flagellum	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0003698	abnormal male reproductive system physiology	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0009838	abnormal sperm axoneme morphology	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0031356	abnormal outer dense fiber morphology	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0031410	biflagellated sperm	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0009237	kinked sperm flagellum	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0008898	abnormal acrosome morphology	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0009280	decreased activated sperm motility	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0002686	globozoospermia	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0031352	absent sperm axonemal central pair	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461175	M	MP:0030978	impaired binding of sperm to zona pellucida	Pla2g3<tm1Murm>/Pla2g3<tm1Murm>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461176	M	MP:0001922	reduced male fertility	Pla2g3<tm1Murm>/Pla2g3<+>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461176	M	MP:0009280	decreased activated sperm motility	Pla2g3<tm1Murm>/Pla2g3<+>	involves: 129S/SvEv * C57BL/6J	N	20424323
MGI:4461177	M	MP:0003698	abnormal male reproductive system physiology	Pla2g10<tm1Kiku>/Pla2g10<tm1Kiku>	involves: 129P2/OlaHsd	N	20424323
MGI:4461249	M	MP:0009199	abnormal external male genitalia morphology	Ar<tm2Ska>/Y,Gli1<tm3(cre/ERT2)Alj>/Gli1<+>	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	19282366
MGI:4461249	M	MP:0003553	abnormal foreskin morphology	Ar<tm2Ska>/Y,Gli1<tm3(cre/ERT2)Alj>/Gli1<+>	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	19282366
MGI:4461249	M	MP:0003936	abnormal reproductive system development	Ar<tm2Ska>/Y,Gli1<tm3(cre/ERT2)Alj>/Gli1<+>	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	19282366
MGI:4461250	M	MP:0009199	abnormal external male genitalia morphology	Ctnnb1<tm4Wbm>/Ctnnb1<tm4Wbm>,Gli1<tm3(cre/ERT2)Alj>/Gli1<+>	involves: 129P2/OlaHsd * 129S6/SvEvTac	N	19282366
MGI:4461250	M	MP:0003553	abnormal foreskin morphology	Ctnnb1<tm4Wbm>/Ctnnb1<tm4Wbm>,Gli1<tm3(cre/ERT2)Alj>/Gli1<+>	involves: 129P2/OlaHsd * 129S6/SvEvTac	N	19282366
MGI:4461251	F	MP:0003126	abnormal external female genitalia morphology	Ctnnb1<tm1Mmt>/Ctnnb1<tm1Mmt>,Gli1<tm3(cre/ERT2)Alj>/Gli1<+>	involves: 129S6/SvEvTac * 129X1/SvJ	N	19282366
MGI:4461252	M	MP:0005389	reproductive system phenotype	Ar<tm2Ska>/Y,Tg(KRT5-cre)1Tak/0	involves: C3H * C57BL/6 * CBA	Y	19282366
MGI:4461253	M	MP:0005389	reproductive system phenotype	Ar<tm2Ska>/Y,Shh<tm2(cre/ERT2)Cjt>/Shh<+>	involves: 129S6/SvEvTac * C57BL/6 * CBA	Y	19282366
MGI:4461268	F	MP:0001973	increased thermal nociceptive threshold	Git2<Gt(XG510)Byg>/Git2<Gt(XG510)Byg>	B6.129P2-Git2<Gt(XG510)Byg>	N	23870131
MGI:4461323	M	MP:0008279	arrest of spermiogenesis	t<AE5>/t<AE5>	Not Specified	N	1003081
MGI:4461323	M	MP:0001156	abnormal spermatogenesis	t<AE5>/t<AE5>	Not Specified	N	1003081
MGI:4461462	F	MP:0014126	increased mammary gland apoptosis	Foxa1<tm1Gsc>/Foxa1<+>	involves: 129P2/OlaHsd	N	20501593
MGI:4461462	F	MP:0000662	abnormal branching of the mammary ductal tree	Foxa1<tm1Gsc>/Foxa1<+>	involves: 129P2/OlaHsd	N	20501593
MGI:4461790	M	MP:0009239	short sperm flagellum	Ttll1<tm1Seto>/Ttll1<tm1Seto>	involves: 129S/SvEv * C57BL/6	N	20498047
MGI:4462240	F	MP:0001923	reduced female fertility	Tg(RP23-326M22)760She/0	B6.Cg-Tg(RP23-326M22)760She	N	18285828
MGI:4462243	M	MP:0001922	reduced male fertility	Tg(RP23-326M22)760She/Tg(RP23-326M22)760She	B6.Cg-Tg(RP23-326M22)760She	N	18285828
MGI:4462243	F	MP:0001923	reduced female fertility	Tg(RP23-326M22)760She/Tg(RP23-326M22)760She	B6.Cg-Tg(RP23-326M22)760She	N	18285828
MGI:4462246	M	MP:0003171	phenotypic reversion	Hprt1<tm1Dwm>/Y	involves: 129P2/OlaHsd	N	2912572
MGI:4462247	F	MP:0003171	phenotypic reversion	Hprt1<tm1Dwm>/Hprt1<b-m3>	involves: 129P2/OlaHsd	N	2912572
MGI:4462356	M	MP:0001922	reduced male fertility	Zbtb16<pnky>/Zbtb16<pnky>	CBA/CaJAnu-Zbtb16<pnky>/Apb	N	MGI:3611487
MGI:4462419	F	MP:0005385	cardiovascular system phenotype	Add3<tm1.2Llp>/Add3<tm1.2Llp>	129S1.129P2(B6)-Add3<tm1.2Llp>	Y	19425068
MGI:4462712	F	MP:0001144	vagina atresia	Vangl2<Lp-2J>/Vangl2<+>	B6.Cg-Vangl2<Lp-2J>/GrsrJ	N	MGI:4462048
MGI:4462795	M	MP:0008893	detached sperm flagellum	Oaz3<tm1Htan>/Oaz3<tm1Htan>	involves: 129S1/Sv * C57BL/6	N	19893612
MGI:4462795	M	MP:0001925	male infertility	Oaz3<tm1Htan>/Oaz3<tm1Htan>	involves: 129S1/Sv * C57BL/6	N	19893612
MGI:4462795	M	MP:0004542	impaired acrosome reaction	Oaz3<tm1Htan>/Oaz3<tm1Htan>	involves: 129S1/Sv * C57BL/6	N	19893612
MGI:4818425	F	MP:0003633	abnormal nervous system physiology	Sh3kbp1<tm1Ivdi>/Sh3kbp1<tm1Ivdi>	B6.129S-Sh3kbp1<tm1Ivdi>	N	20551902
MGI:4818425	F	MP:0031391	increased locomotor activity	Sh3kbp1<tm1Ivdi>/Sh3kbp1<tm1Ivdi>	B6.129S-Sh3kbp1<tm1Ivdi>	N	20551902
MGI:4818425	F	MP:0008844	decreased subcutaneous adipose tissue amount	Sh3kbp1<tm1Ivdi>/Sh3kbp1<tm1Ivdi>	B6.129S-Sh3kbp1<tm1Ivdi>	N	20551902
MGI:4818425	F	MP:0009745	abnormal behavioral response to xenobiotic	Sh3kbp1<tm1Ivdi>/Sh3kbp1<tm1Ivdi>	B6.129S-Sh3kbp1<tm1Ivdi>	N	20551902
MGI:4818425	F	MP:0005449	abnormal food intake	Sh3kbp1<tm1Ivdi>/Sh3kbp1<tm1Ivdi>	B6.129S-Sh3kbp1<tm1Ivdi>	N	20551902
MGI:4818425	F	MP:0001906	increased dopamine level	Sh3kbp1<tm1Ivdi>/Sh3kbp1<tm1Ivdi>	B6.129S-Sh3kbp1<tm1Ivdi>	N	20551902
MGI:4818425	F	MP:0003960	increased lean body mass	Sh3kbp1<tm1Ivdi>/Sh3kbp1<tm1Ivdi>	B6.129S-Sh3kbp1<tm1Ivdi>	N	20551902
MGI:4818425	F	MP:0001415	increased exploration in new environment	Sh3kbp1<tm1Ivdi>/Sh3kbp1<tm1Ivdi>	B6.129S-Sh3kbp1<tm1Ivdi>	N	20551902
MGI:4818608	F	MP:0000627	abnormal mammary gland morphology	Chek1<tm2.1Sje>/Chek1<+>,Tg(MMTV-cre)#Mam/0	involves: FVB	N	20473325
MGI:4818608	F	MP:0009506	abnormal mammary gland alveolus morphology	Chek1<tm2.1Sje>/Chek1<+>,Tg(MMTV-cre)#Mam/0	involves: FVB	N	20473325
MGI:4818609	F	MP:0000627	abnormal mammary gland morphology	Chek1<tm2.1Sje>/Chek1<tm2.1Sje>,Tg(MMTV-cre)#Mam/0	involves: FVB	N	20473325
MGI:4818609	F	MP:0009506	abnormal mammary gland alveolus morphology	Chek1<tm2.1Sje>/Chek1<tm2.1Sje>,Tg(MMTV-cre)#Mam/0	involves: FVB	N	20473325
MGI:4818610	F	MP:0009506	abnormal mammary gland alveolus morphology	Chek1<tm2.1Sje>/Chek1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(MMTV-cre)#Mam/0	involves: 129P2/OlaHsd * FVB	N	20473325
MGI:4818610	F	MP:0000630	mammary gland hyperplasia	Chek1<tm2.1Sje>/Chek1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(MMTV-cre)#Mam/0	involves: 129P2/OlaHsd * FVB	N	20473325
MGI:4818615	F	MP:0009506	abnormal mammary gland alveolus morphology	Chek1<tm2.1Sje>/Chek1<tm2.1Sje>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(MMTV-cre)#Mam/0	involves: 129P2/OlaHsd * FVB	N	20473325
MGI:4818618	F	MP:0009506	abnormal mammary gland alveolus morphology	Chek1<tm2.1Sje>/Chek1<tm2.1Sje>,Trp53<tm1Brn>/Trp53<+>,Tg(MMTV-cre)#Mam/0	involves: 129P2/OlaHsd * FVB	N	20473325
MGI:4818619	F	MP:0000630	mammary gland hyperplasia	Chek1<tm2.1Sje>/Chek1<+>,Trp53<tm1Brn>/Trp53<+>,Tg(MMTV-cre)#Mam/0	involves: 129P2/OlaHsd * FVB	N	20473325
MGI:4818619	F	MP:0000662	abnormal branching of the mammary ductal tree	Chek1<tm2.1Sje>/Chek1<+>,Trp53<tm1Brn>/Trp53<+>,Tg(MMTV-cre)#Mam/0	involves: 129P2/OlaHsd * FVB	N	20473325
MGI:4818619	F	MP:0009506	abnormal mammary gland alveolus morphology	Chek1<tm2.1Sje>/Chek1<+>,Trp53<tm1Brn>/Trp53<+>,Tg(MMTV-cre)#Mam/0	involves: 129P2/OlaHsd * FVB	N	20473325
MGI:4818913	M	MP:0002631	abnormal epididymis morphology	Mei4<tm1Bdm>/Mei4<tm1Bdm>	involves: 129S2/SvPas	N	20551173
MGI:4818913	M	MP:0009205	abnormal internal male genitalia morphology	Mei4<tm1Bdm>/Mei4<tm1Bdm>	involves: 129S2/SvPas	N	20551173
MGI:4818913	F	MP:0011121	decreased primordial ovarian follicle number	Mei4<tm1Bdm>/Mei4<tm1Bdm>	involves: 129S2/SvPas	N	20551173
MGI:4818913	M	MP:0005159	azoospermia	Mei4<tm1Bdm>/Mei4<tm1Bdm>	involves: 129S2/SvPas	N	20551173
MGI:4818913	M	MP:0008261	arrest of male meiosis	Mei4<tm1Bdm>/Mei4<tm1Bdm>	involves: 129S2/SvPas	N	20551173
MGI:4818913	M	MP:0006379	abnormal spermatocyte morphology	Mei4<tm1Bdm>/Mei4<tm1Bdm>	involves: 129S2/SvPas	N	31000436
MGI:4818913	M	MP:0004852	decreased testis weight	Mei4<tm1Bdm>/Mei4<tm1Bdm>	involves: 129S2/SvPas	N	20551173
MGI:4818913	F	MP:0008871	abnormal ovarian follicle number	Mei4<tm1Bdm>/Mei4<tm1Bdm>	involves: 129S2/SvPas	N	20551173
MGI:4818913	M	MP:0001146	abnormal testis morphology	Mei4<tm1Bdm>/Mei4<tm1Bdm>	involves: 129S2/SvPas	N	20551173
MGI:4818913	F	MP:0011125	decreased primary ovarian follicle number	Mei4<tm1Bdm>/Mei4<tm1Bdm>	involves: 129S2/SvPas	N	20551173
MGI:4818913	M	MP:0013601	increased testis apoptosis	Mei4<tm1Bdm>/Mei4<tm1Bdm>	involves: 129S2/SvPas	N	20551173
MGI:4818913	M	MP:0002216	abnormal seminiferous tubule morphology	Mei4<tm1Bdm>/Mei4<tm1Bdm>	involves: 129S2/SvPas	N	20551173
MGI:4819010	M	MP:0005578	teratozoospermia	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas	N	20624957
MGI:4819010	M	MP:0002216	abnormal seminiferous tubule morphology	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas	N	20624957
MGI:4819010	M	MP:0009239	short sperm flagellum	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas	N	20624957
MGI:4819010	M	MP:0009230	abnormal sperm head morphology	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas	N	20624957
MGI:4819010	M	MP:0009238	coiled sperm flagellum	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas	N	20624957
MGI:4819010	M	MP:0001147	small testis	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas	N	20624957
MGI:4819010	M	MP:0001925	male infertility	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas	N	20624957
MGI:4819010	M	MP:0004901	decreased male germ cell number	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas	N	20624957
MGI:4819119	F	MP:0001805	decreased IgG level	Cd40lg<m1Btlr>/Cd40lg<m1Btlr>	C57BL/6J-Cd40lg<m1Btlr>	N	MGI:4818252
MGI:4819119	F	MP:0005387	immune system phenotype	Cd40lg<m1Btlr>/Cd40lg<m1Btlr>	C57BL/6J-Cd40lg<m1Btlr>	Y	MGI:4818252
MGI:4819121	F	MP:0001885	mammary gland duct hyperplasia	Tg(Wnt1)1Hev/0	involves: C57BL/6 * SJL	N	10713683
MGI:4819175	M	MP:0000371	diluted coat color	Atp7a<Mo-pew2J>/Y	involves: C57BL/6J * SJL/J	N	MGI:64397
MGI:4819175	M	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-pew2J>/Y	involves: C57BL/6J * SJL/J	N	MGI:64397
MGI:4819175	M	MP:0010768	mortality/aging	Atp7a<Mo-pew2J>/Y	involves: C57BL/6J * SJL/J	Y	MGI:64397
MGI:4819180	F	MP:0000421	mottled coat	Atp7a<Mo-pew2J>/Atp7a<+>	involves: C57BL/6J * SJL/J	N	MGI:64397
MGI:4819180	F	MP:0000372	irregular coat pigmentation	Atp7a<Mo-pew2J>/Atp7a<+>	involves: C57BL/6J * SJL/J	N	MGI:64397
MGI:4819180	F	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-pew2J>/Atp7a<+>	involves: C57BL/6J * SJL/J	N	MGI:64397
MGI:4819192	M	MP:0003607	abnormal prostate gland physiology	Brca2<tm1Brn>/Brca2<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	20585617
MGI:4819192	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Brca2<tm1Brn>/Brca2<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	20585617
MGI:4819192	M	MP:0000659	prostate gland hyperplasia	Brca2<tm1Brn>/Brca2<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	20585617
MGI:4819193	M	MP:0000659	prostate gland hyperplasia	Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	20585617
MGI:4819193	M	MP:0003607	abnormal prostate gland physiology	Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	20585617
MGI:4819193	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	20585617
MGI:4819194	M	MP:0001158	abnormal prostate gland morphology	Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<+>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	20585617
MGI:4819194	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<+>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	20585617
MGI:4819194	M	MP:0003607	abnormal prostate gland physiology	Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<+>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	N	20585617
MGI:4819553	M	MP:0001146	abnormal testis morphology	Ctcfl<tm1Vloc>/Ctcfl<tm1Vloc>	involves: 129S1/Sv * C57BL/6	N	20231363
MGI:4819553	M	MP:0001147	small testis	Ctcfl<tm1Vloc>/Ctcfl<tm1Vloc>	involves: 129S1/Sv * C57BL/6	N	20231363
MGI:4819553	M	MP:0008280	abnormal male germ cell apoptosis	Ctcfl<tm1Vloc>/Ctcfl<tm1Vloc>	involves: 129S1/Sv * C57BL/6	N	20231363
MGI:4819553	M	MP:0001156	abnormal spermatogenesis	Ctcfl<tm1Vloc>/Ctcfl<tm1Vloc>	involves: 129S1/Sv * C57BL/6	N	20231363
MGI:4819553	M	MP:0005169	abnormal male meiosis	Ctcfl<tm1Vloc>/Ctcfl<tm1Vloc>	involves: 129S1/Sv * C57BL/6	N	20231363
MGI:4819553	M	MP:0001940	testis hypoplasia	Ctcfl<tm1Vloc>/Ctcfl<tm1Vloc>	involves: 129S1/Sv * C57BL/6	N	20231363
MGI:4819554	M	MP:0001146	abnormal testis morphology	Ctcfl<tm1.1Vloc>/Ctcfl<tm1.1Vloc>	involves: 129S1/Sv * C57BL/6 * SJL	N	20231363
MGI:4819554	M	MP:0001156	abnormal spermatogenesis	Ctcfl<tm1.1Vloc>/Ctcfl<tm1.1Vloc>	involves: 129S1/Sv * C57BL/6 * SJL	N	20231363
MGI:4819599	F	MP:0001926	female infertility	Vangl1<Gt(XL802)Byg>/Vangl1<Gt(XL802)Byg>,Vangl2<Lp>/Vangl2<+>	involves: 129P2/OlaHsd * A	N	20562861
MGI:4819599	F	MP:0001144	vagina atresia	Vangl1<Gt(XL802)Byg>/Vangl1<Gt(XL802)Byg>,Vangl2<Lp>/Vangl2<+>	involves: 129P2/OlaHsd * A	N	20562861
MGI:4819737	F	MP:0002566	abnormal sexual interaction	Vmn2r116<tm1.1Ktou>/Vmn2r116<tm1.1Ktou>	C57BL/6-Vmn2r116<tm1.1Ktou>	N	20596023
MGI:4819738	F	MP:0002566	abnormal sexual interaction	Trpc2<tm1Rax>/Trpc2<tm1Rax>	involves: 129S/SvEv	N	20596023
MGI:4819766	M	MP:0001925	male infertility	Cimap3<tm1.1Heli>/Cimap3<+>	chimera involves: 129S6/SvEvTac * C57BL/6J	N	20643351
MGI:4820562	F	MP:0003058	increased insulin secretion	Pgr<tm1Bwo>/Pgr<tm1Bwo>	involves: 129S7/SvEvBrd * C57BL/6J	N	12438645
MGI:4820562	F	MP:0011819	increased pancreatic beta cell proliferation	Pgr<tm1Bwo>/Pgr<tm1Bwo>	involves: 129S7/SvEvBrd * C57BL/6J	N	12438645
MGI:4820562	F	MP:0005491	pancreatic islet hyperplasia	Pgr<tm1Bwo>/Pgr<tm1Bwo>	involves: 129S7/SvEvBrd * C57BL/6J	N	12438645
MGI:4820562	F	MP:0005560	decreased circulating glucose level	Pgr<tm1Bwo>/Pgr<tm1Bwo>	involves: 129S7/SvEvBrd * C57BL/6J	N	12438645
MGI:4820562	F	MP:0002079	increased circulating insulin level	Pgr<tm1Bwo>/Pgr<tm1Bwo>	involves: 129S7/SvEvBrd * C57BL/6J	N	12438645
MGI:4820562	F	MP:0003645	increased pancreatic beta cell number	Pgr<tm1Bwo>/Pgr<tm1Bwo>	involves: 129S7/SvEvBrd * C57BL/6J	N	12438645
MGI:4820562	F	MP:0005292	improved glucose tolerance	Pgr<tm1Bwo>/Pgr<tm1Bwo>	involves: 129S7/SvEvBrd * C57BL/6J	N	12438645
MGI:4820598	F	MP:0001923	reduced female fertility	Slc11a2<mk>/Slc11a2<mk>	SEC.Cg-Slc11a2<mk>	N	5427253
MGI:4820732	F	MP:0002493	increased IgG level	Btk<vila>/Btk<vila>	C57BL/6JAnu-Btk<vila>/AnuApb	N	MGI:3611487
MGI:4820732	F	MP:0005017	decreased B cell number	Btk<vila>/Btk<vila>	C57BL/6JAnu-Btk<vila>/AnuApb	N	MGI:3611487
MGI:4820732	F	MP:0002491	decreased IgD level	Btk<vila>/Btk<vila>	C57BL/6JAnu-Btk<vila>/AnuApb	N	MGI:3611487
MGI:4820732	F	MP:0002497	increased IgE level	Btk<vila>/Btk<vila>	C57BL/6JAnu-Btk<vila>/AnuApb	N	MGI:3611487
MGI:4820732	F	MP:0008246	abnormal leukocyte morphology	Btk<vila>/Btk<vila>	C57BL/6JAnu-Btk<vila>/AnuApb	N	MGI:3611487
MGI:4820818	F	MP:0009758	impaired behavioral response to cocaine	Gprasp1<tm1.1Jlw>/Gprasp1<tm1.1Jlw>	involves: C57BL/6	N	20543951
MGI:4820830	F	MP:0001926	female infertility	Traf3ip2<adjm>/Traf3ip2<adjm>	KOR-Traf3ip2<adjm>	N	20660351
MGI:4820835	M	MP:0009230	abnormal sperm head morphology	Dynlt2a1<tm1June>/Dynlt2a1<tm1June>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19778998
MGI:4820835	M	MP:0004852	decreased testis weight	Dynlt2a1<tm1June>/Dynlt2a1<tm1June>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19778998
MGI:4820835	M	MP:0008892	abnormal sperm flagellum morphology	Dynlt2a1<tm1June>/Dynlt2a1<tm1June>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19778998
MGI:4820835	M	MP:0001155	arrest of spermatogenesis	Dynlt2a1<tm1June>/Dynlt2a1<tm1June>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19778998
MGI:4820835	M	MP:0002675	asthenozoospermia	Dynlt2a1<tm1June>/Dynlt2a1<tm1June>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19778998
MGI:4820835	M	MP:0001925	male infertility	Dynlt2a1<tm1June>/Dynlt2a1<tm1June>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19778998
MGI:4820835	M	MP:0009839	multiflagellated sperm	Dynlt2a1<tm1June>/Dynlt2a1<tm1June>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19778998
MGI:4820835	M	MP:0002687	oligozoospermia	Dynlt2a1<tm1June>/Dynlt2a1<tm1June>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19778998
MGI:4820835	M	MP:0008280	abnormal male germ cell apoptosis	Dynlt2a1<tm1June>/Dynlt2a1<tm1June>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	19778998
MGI:4820963	M	MP:0001925	male infertility	t<0>/t<wPas1>	involves: M. m. brevirostris	N	7461454
MGI:4820964	M	MP:0001925	male infertility	t<w1>/t<wPas1>	involves: M. m. brevirostris	N	7461454
MGI:4820966	M	MP:0001925	male infertility	t<w5>/t<wPas1>	involves: M. m. brevirostris	N	7461454
MGI:4820967	M	MP:0001925	male infertility	t<9>/t<wPas1>	involves: M. m. brevirostris	N	7461454
MGI:4820969	M	MP:0001925	male infertility	t<12>/t<wPas1>	involves: M. m. brevirostris	N	7461454
MGI:4820970	M	MP:0001925	male infertility	t<w73>/t<wPas1>	involves: M. m. brevirostris * M. m. musculus	N	7461454
MGI:4821123	M	MP:0001163	abnormal prostate gland anterior lobe morphology	Wdr77<tm2Zwan>/Wdr77<tm2Zwan>,Tg(Pbsn-cre)20Fwan/0	involves: C57BL/6J * FVB/NCrl	N	20519372
MGI:4821123	M	MP:0009734	abnormal prostate gland duct morphology	Wdr77<tm2Zwan>/Wdr77<tm2Zwan>,Tg(Pbsn-cre)20Fwan/0	involves: C57BL/6J * FVB/NCrl	N	20519372
MGI:4821123	M	MP:0009735	abnormal prostate gland development	Wdr77<tm2Zwan>/Wdr77<tm2Zwan>,Tg(Pbsn-cre)20Fwan/0	involves: C57BL/6J * FVB/NCrl	N	20519372
MGI:4821123	M	MP:0009736	abnormal prostate gland branching morphogenesis	Wdr77<tm2Zwan>/Wdr77<tm2Zwan>,Tg(Pbsn-cre)20Fwan/0	involves: C57BL/6J * FVB/NCrl	N	20519372
MGI:4821123	M	MP:0003607	abnormal prostate gland physiology	Wdr77<tm2Zwan>/Wdr77<tm2Zwan>,Tg(Pbsn-cre)20Fwan/0	involves: C57BL/6J * FVB/NCrl	N	20519372
MGI:4821123	M	MP:0001168	abnormal prostate gland epithelium morphology	Wdr77<tm2Zwan>/Wdr77<tm2Zwan>,Tg(Pbsn-cre)20Fwan/0	involves: C57BL/6J * FVB/NCrl	N	20519372
MGI:4821123	M	MP:0001167	prostate gland epithelial hyperplasia	Wdr77<tm2Zwan>/Wdr77<tm2Zwan>,Tg(Pbsn-cre)20Fwan/0	involves: C57BL/6J * FVB/NCrl	N	20519372
MGI:4821123	M	MP:0002774	small prostate gland	Wdr77<tm2Zwan>/Wdr77<tm2Zwan>,Tg(Pbsn-cre)20Fwan/0	involves: C57BL/6J * FVB/NCrl	N	20519372
MGI:4821123	M	MP:0000666	decreased prostate gland duct number	Wdr77<tm2Zwan>/Wdr77<tm2Zwan>,Tg(Pbsn-cre)20Fwan/0	involves: C57BL/6J * FVB/NCrl	N	20519372
MGI:4821123	M	MP:0009381	abnormal prostate gland dorsolateral lobe morphology	Wdr77<tm2Zwan>/Wdr77<tm2Zwan>,Tg(Pbsn-cre)20Fwan/0	involves: C57BL/6J * FVB/NCrl	N	20519372
MGI:4821123	M	MP:0009380	abnormal prostate gland ventral lobe morphology	Wdr77<tm2Zwan>/Wdr77<tm2Zwan>,Tg(Pbsn-cre)20Fwan/0	involves: C57BL/6J * FVB/NCrl	N	20519372
MGI:4821152	M	MP:0001925	male infertility	t<wPas2>/t<wPas2>	involves: M. m. brevirostris	N	7461454
MGI:4821261	F	MP:0010401	increased skeletal muscle glycogen level	Phka1<I/FnLn>/Phka1<I/FnLn>	I/FnLn	N	5444100
MGI:4821269	M	MP:0001925	male infertility	t<wPas3>/t<wPas3>	involves: M. m. domesticus	N	7461454
MGI:4821270	F	MP:0010401	increased skeletal muscle glycogen level	Phka1<I/FnLn>/Phka1<+>	(C57BL/FnLn x I/FnLn)F1	N	5444100
MGI:4821272	F	MP:0010401	increased skeletal muscle glycogen level	Phka1<I/FnLn>/Phka1<+>	(I/FnLn x C57BL/FnLn)F1	N	5444100
MGI:4821273	M	MP:0010401	increased skeletal muscle glycogen level	Phka1<I/FnLn>/Y	(I/FnLn x C57BL/FnLn)F1	N	5444100
MGI:4821274	M	MP:0010401	increased skeletal muscle glycogen level	Phka1<I/FnLn>/Y	I/FnLn	N	5444100
MGI:4821283	F	MP:0003960	increased lean body mass	Dll1<m1Mhda>/Dll1<+>	C3HeB/FeJ-Dll1<m1Mhda>	N	19562077
MGI:4821283	F	MP:0001399	hyperactivity	Dll1<m1Mhda>/Dll1<+>	C3HeB/FeJ-Dll1<m1Mhda>	N	19562077
MGI:4821283	M	MP:0002644	decreased circulating triglyceride level	Dll1<m1Mhda>/Dll1<+>	C3HeB/FeJ-Dll1<m1Mhda>	N	19562077
MGI:4821283	F	MP:0006143	increased systemic arterial diastolic blood pressure	Dll1<m1Mhda>/Dll1<+>	C3HeB/FeJ-Dll1<m1Mhda>	N	19562077
MGI:4821283	F	MP:0006144	increased systemic arterial systolic blood pressure	Dll1<m1Mhda>/Dll1<+>	C3HeB/FeJ-Dll1<m1Mhda>	N	19562077
MGI:4821283	F	MP:0004875	increased mean systemic arterial blood pressure	Dll1<m1Mhda>/Dll1<+>	C3HeB/FeJ-Dll1<m1Mhda>	N	19562077
MGI:4821283	M	MP:0005179	decreased circulating cholesterol level	Dll1<m1Mhda>/Dll1<+>	C3HeB/FeJ-Dll1<m1Mhda>	N	19562077
MGI:4821310	M	MP:0001922	reduced male fertility	sb/sb	involves: CF-1	N	MGI:48783
MGI:4821310	F	MP:0001923	reduced female fertility	sb/sb	involves: CF-1	N	MGI:48783
MGI:4821353	M	MP:0002152	abnormal brain morphology	Huwe1<tm1Alas>/Y,Tg(Nes-cre)1Kag/0	involves: 129S7/SvEvBrd	N	19686682
MGI:4821353	M	MP:0002058	neonatal lethality	Huwe1<tm1Alas>/Y,Tg(Nes-cre)1Kag/0	involves: 129S7/SvEvBrd	N	19686682
MGI:4821353	M	MP:0004980	increased neuronal precursor cell number	Huwe1<tm1Alas>/Y,Tg(Nes-cre)1Kag/0	involves: 129S7/SvEvBrd	N	19686682
MGI:4821353	M	MP:0004948	abnormal neuronal precursor proliferation	Huwe1<tm1Alas>/Y,Tg(Nes-cre)1Kag/0	involves: 129S7/SvEvBrd	N	19686682
MGI:4821353	M	MP:0000852	small cerebellum	Huwe1<tm1Alas>/Y,Tg(Nes-cre)1Kag/0	involves: 129S7/SvEvBrd	N	19686682
MGI:4821353	M	MP:0000812	abnormal dentate gyrus morphology	Huwe1<tm1Alas>/Y,Tg(Nes-cre)1Kag/0	involves: 129S7/SvEvBrd	N	19686682
MGI:4821353	M	MP:0000790	abnormal stratification in cerebral cortex	Huwe1<tm1Alas>/Y,Tg(Nes-cre)1Kag/0	involves: 129S7/SvEvBrd	N	19686682
MGI:4821353	M	MP:0000788	abnormal cerebral cortex morphology	Huwe1<tm1Alas>/Y,Tg(Nes-cre)1Kag/0	involves: 129S7/SvEvBrd	N	19686682
MGI:4821353	M	MP:0000774	decreased brain size	Huwe1<tm1Alas>/Y,Tg(Nes-cre)1Kag/0	involves: 129S7/SvEvBrd	N	19686682
MGI:4821353	M	MP:0006254	thin cerebral cortex	Huwe1<tm1Alas>/Y,Tg(Nes-cre)1Kag/0	involves: 129S7/SvEvBrd	N	19686682
MGI:4821397	M	MP:0009828	increased tumor latency	Egr1<tm1Jmi>/Egr1<tm1Jmi>,Tg(TRAMP)8247Ng/?	involves: 129 * C57BL/6	N	11135623
MGI:4821788	F	MP:0001106	abnormal Schwann cell morphology	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae	N	9169515
MGI:4821788	F	MP:0005404	abnormal axon morphology	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae	N	9169515
MGI:4821788	F	MP:0003632	abnormal nervous system morphology	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae	N	9169515
MGI:4821788	F	MP:0005403	abnormal nerve conduction	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae	N	9169515
MGI:4821788	F	MP:0000921	demyelination	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae	N	9169515
MGI:4821788	F	MP:0005386	behavior/neurological phenotype	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae	Y	9169515
MGI:4821788	F	MP:0000920	abnormal myelination	Gjb1<tm1Kwi>/Gjb1<tm1Kwi>	involves: 129S4/SvJae	N	9169515
MGI:4821790	M	MP:0001106	abnormal Schwann cell morphology	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae	N	9169515
MGI:4821790	M	MP:0005404	abnormal axon morphology	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae	N	9169515
MGI:4821790	M	MP:0000920	abnormal myelination	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae	N	9169515
MGI:4821790	M	MP:0000921	demyelination	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae	N	9169515
MGI:4821790	M	MP:0005386	behavior/neurological phenotype	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae	Y	9169515
MGI:4821790	M	MP:0005403	abnormal nerve conduction	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae	N	9169515
MGI:4821790	M	MP:0003632	abnormal nervous system morphology	Gjb1<tm1Kwi>/Y	involves: 129S4/SvJae	N	9169515
MGI:4821791	F	MP:0000921	demyelination	Gjb1<tm1Kwi>/Gjb1<+>	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:4821791	F	MP:0003871	abnormal myelin sheath morphology	Gjb1<tm1Kwi>/Gjb1<+>	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:4821791	F	MP:0001106	abnormal Schwann cell morphology	Gjb1<tm1Kwi>/Gjb1<+>	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:4821791	F	MP:0003632	abnormal nervous system morphology	Gjb1<tm1Kwi>/Gjb1<+>	involves: 129S4/SvJae * C57BL/6	N	9700485
MGI:4821831	M	MP:0002674	abnormal sperm motility	Prkaca<tm4.1Gsm>/Prkaca<tm4.1Gsm>	involves: C57BL/6	N	19074277
MGI:4822200	M	MP:0002216	abnormal seminiferous tubule morphology	Kit<W-3Bao>/Kit<+>	involves: C57BL/6J	N	20536544
MGI:4822201	M	MP:0002216	abnormal seminiferous tubule morphology	Kit<W-2Bao>/Kit<+>	involves: C57BL/6J	N	20536544
MGI:4822202	M	MP:0002216	abnormal seminiferous tubule morphology	Kit<W-3Bao>/Kit<W-3Bao>	involves: C57BL/6J	N	20536544
MGI:4822202	M	MP:0003698	abnormal male reproductive system physiology	Kit<W-3Bao>/Kit<W-3Bao>	involves: C57BL/6J	N	20536544
MGI:4822202	F	MP:0009361	abnormal primordial ovarian follicle morphology	Kit<W-3Bao>/Kit<W-3Bao>	involves: C57BL/6J	N	20536544
MGI:4822203	M	MP:0002216	abnormal seminiferous tubule morphology	Kit<Wads>/Kit<+>	involves: C57BL/6J	N	20536544
MGI:4822383	M	MP:0004852	decreased testis weight	Tpst2<grt>/Tpst2<grt>	involves: DW/JMuaf	N	18075202
MGI:4822383	M	MP:0002216	abnormal seminiferous tubule morphology	Tpst2<grt>/Tpst2<grt>	involves: DW/JMuaf	N	18075202
MGI:4822383	M	MP:0005159	azoospermia	Tpst2<grt>/Tpst2<grt>	involves: DW/JMuaf	N	18075202
MGI:4822383	M	MP:0001153	small seminiferous tubules	Tpst2<grt>/Tpst2<grt>	involves: DW/JMuaf	N	18075202
MGI:4822555	F	MP:0009503	abnormal mammary gland duct morphology	Adam17<tm1.1Srj>/Adam17<tm1.1Srj>	involves: 129S/SvEv * C57BL/6 * SJL	N	20603312
MGI:4822562	M	MP:0001922	reduced male fertility	Chdh<tm1Zei>/Chdh<tm1Zei>	involves: 129P2/OlaHsd * C57BL/6	N	20371614
MGI:4822562	M	MP:0002675	asthenozoospermia	Chdh<tm1Zei>/Chdh<tm1Zei>	involves: 129P2/OlaHsd * C57BL/6	N	20371614
MGI:4822575	F	MP:0001926	female infertility	sims/sims	B6.Cg-sims/GrsrJ	N	MGI:4459517
MGI:4822575	M	MP:0001925	male infertility	sims/sims	B6.Cg-sims/GrsrJ	N	MGI:4459517
MGI:4822575	F	MP:0002637	small uterus	sims/sims	B6.Cg-sims/GrsrJ	N	MGI:4459517
MGI:4829517	F	MP:0001382	abnormal nursing	M4.8.4Djba/M4.8.4Djba<+>	C3H/HeJ-M4.8.4Djba	N	14499351
MGI:4829790	M	MP:0002628	hepatic steatosis	Pten<tm1Hwu>/Pten<tm1Hwu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S4/SvJae * C57BL/6 * DBA	N	20837017
MGI:4829790	M	MP:0003674	oxidative stress	Pten<tm1Hwu>/Pten<tm1Hwu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S4/SvJae * C57BL/6 * DBA	N	20837017
MGI:4829790	M	MP:0010315	increased cholangiocarcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S4/SvJae * C57BL/6 * DBA	N	20837017
MGI:4829790	M	MP:0003887	increased hepatocyte apoptosis	Pten<tm1Hwu>/Pten<tm1Hwu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S4/SvJae * C57BL/6 * DBA	N	20837017
MGI:4829790	M	MP:0000598	abnormal liver morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S4/SvJae * C57BL/6 * DBA	N	20837017
MGI:4829790	M	MP:0002941	increased circulating alanine transaminase level	Pten<tm1Hwu>/Pten<tm1Hwu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S4/SvJae * C57BL/6 * DBA	N	20837017
MGI:4829790	M	MP:0003331	increased hepatocellular carcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S4/SvJae * C57BL/6 * DBA	N	20837017
MGI:4829790	M	MP:0003893	increased hepatocyte proliferation	Pten<tm1Hwu>/Pten<tm1Hwu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S4/SvJae * C57BL/6 * DBA	N	20837017
MGI:4829790	M	MP:0008019	increased liver tumor incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S4/SvJae * C57BL/6 * DBA	N	20837017
MGI:4829793	F	MP:0001885	mammary gland duct hyperplasia	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(MMTV-cre)4Mam/0	involves: 129S4/SvJae * FVB	N	12163417
MGI:4829793	F	MP:0000662	abnormal branching of the mammary ductal tree	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(MMTV-cre)4Mam/0	involves: 129S4/SvJae * FVB	N	12163417
MGI:4829840	F	MP:0005168	abnormal female meiosis	Trip13<Gt(CH0621)Wtsi>/Trip13<Gt(CH0621)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20711356
MGI:4829840	M	MP:0002216	abnormal seminiferous tubule morphology	Trip13<Gt(CH0621)Wtsi>/Trip13<Gt(CH0621)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20711356
MGI:4829840	F	MP:0001129	impaired ovarian folliculogenesis	Trip13<Gt(CH0621)Wtsi>/Trip13<Gt(CH0621)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20711356
MGI:4829840	M	MP:0001147	small testis	Trip13<Gt(CH0621)Wtsi>/Trip13<Gt(CH0621)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20711356
MGI:4829840	M	MP:0008261	arrest of male meiosis	Trip13<Gt(CH0621)Wtsi>/Trip13<Gt(CH0621)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	20711356
MGI:4829882	F	MP:0002169	no abnormal phenotype detected	Tro<tm1Mfu>/Tro<tm1Mfu>	involves: 129S2/SvPas * Black Swiss	N	11804944
MGI:4829883	M	MP:0002169	no abnormal phenotype detected	Tro<tm1Mfu>/Y	involves: 129S2/SvPas * Black Swiss	N	11804944
MGI:4829884	F	MP:0011102	embryonic lethality, incomplete penetrance	Tro<tm1Mfu>/Tro<tm1Mfu>	involves: 129S2/SvPas	N	11804944
MGI:4829885	M	MP:0011102	embryonic lethality, incomplete penetrance	Tro<tm1Mfu>/Y	involves: 129S2/SvPas	N	11804944
MGI:4830138	M	MP:0008892	abnormal sperm flagellum morphology	Entpd5<tm1Rre>/Entpd5<tm1Rre>	involves: 129S5/SvEvBrd * C57BL/6J	N	19176496
MGI:4830138	M	MP:0001925	male infertility	Entpd5<tm1Rre>/Entpd5<tm1Rre>	involves: 129S5/SvEvBrd * C57BL/6J	N	19176496
MGI:4830291	M	MP:0001922	reduced male fertility	Odf2<Gt(XL169)Byg>/Odf2<+>	involves: 129P2/OlaHsd * C57BL/6	N	20550699
MGI:4830291	M	MP:0001925	male infertility	Odf2<Gt(XL169)Byg>/Odf2<+>	involves: 129P2/OlaHsd * C57BL/6	N	20550699
MGI:4830294	M	MP:0009831	abnormal sperm midpiece morphology	Odf2<Gt(XL169)Byg>/Odf2<+>	chimera involves: 129P2/OlaHsd * C57BL/6	N	20550699
MGI:4830294	M	MP:0008892	abnormal sperm flagellum morphology	Odf2<Gt(XL169)Byg>/Odf2<+>	chimera involves: 129P2/OlaHsd * C57BL/6	N	20550699
MGI:4830294	M	MP:0009838	abnormal sperm axoneme morphology	Odf2<Gt(XL169)Byg>/Odf2<+>	chimera involves: 129P2/OlaHsd * C57BL/6	N	20550699
MGI:4830294	M	MP:0009237	kinked sperm flagellum	Odf2<Gt(XL169)Byg>/Odf2<+>	chimera involves: 129P2/OlaHsd * C57BL/6	N	20550699
MGI:4830294	M	MP:0002675	asthenozoospermia	Odf2<Gt(XL169)Byg>/Odf2<+>	chimera involves: 129P2/OlaHsd * C57BL/6	N	20550699
MGI:4830308	M	MP:0001925	male infertility	Cdk5rap2<Gt(RRF465)Byg>/Cdk5rap2<Gt(RRF465)Byg>	involves: 129P2/OlaHsd * C57BL/6J	N	20627074
MGI:4830341	F	MP:0002020	increased tumor incidence	Cxcr3<tm1Wwh>/Cxcr3<tm1Wwh>	Not Specified	N	20713880
MGI:4830462	M	MP:0001405	impaired coordination	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0001732	postnatal growth retardation	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0001505	hunched posture	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0011940	decreased food intake	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0010053	decreased grip strength	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0001429	dehydration	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0001492	abnormal pilomotor reflex	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0001262	decreased body weight	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0004144	hypotonia	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0004889	increased energy expenditure	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0011939	increased food intake	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0011086	postnatal lethality, incomplete penetrance	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0011084	lethality at weaning, incomplete penetrance	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0000421	mottled coat	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830462	M	MP:0001258	decreased body length	Htr2c<tm1.1Eme>/Y	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830463	F	MP:0001262	decreased body weight	Htr2c<tm1.1Eme>/Htr2c<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830463	F	MP:0011940	decreased food intake	Htr2c<tm1.1Eme>/Htr2c<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830463	F	MP:0001732	postnatal growth retardation	Htr2c<tm1.1Eme>/Htr2c<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830464	F	MP:0001732	postnatal growth retardation	Htr2c<tm1.1Eme>/Htr2c<tm1.1Eme>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830464	F	MP:0001262	decreased body weight	Htr2c<tm1.1Eme>/Htr2c<tm1.1Eme>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	20394819
MGI:4830506	M	MP:0002075	abnormal coat/hair pigmentation	Otc<spf-J>/Y	C57BL/6J-Otc<spf-J>/J	N	25647322
MGI:4830506	M	MP:0000416	sparse hair	Otc<spf-J>/Y	C57BL/6J-Otc<spf-J>/J	N	25647322
MGI:4830506	M	MP:0000416	sparse hair	Otc<spf-J>/Y	C57BL/6J-Otc<spf-J>/J	N	MGI:78592
MGI:4830506	M	MP:0005311	abnormal circulating amino acid level	Otc<spf-J>/Y	C57BL/6J-Otc<spf-J>/J	N	25647322
MGI:4830506	M	MP:0009642	abnormal blood homeostasis	Otc<spf-J>/Y	C57BL/6J-Otc<spf-J>/J	N	25647322
MGI:4830506	M	MP:0005332	abnormal amino acid level	Otc<spf-J>/Y	C57BL/6J-Otc<spf-J>/J	N	25647322
MGI:4830506	M	MP:0001265	decreased body size	Otc<spf-J>/Y	C57BL/6J-Otc<spf-J>/J	N	25647322
MGI:4830511	F	MP:0000418	focal hair loss	Otc<spf-J>/Otc<+>	C57BL/6J-Otc<spf-J>/J	N	MGI:78592
MGI:4831150	F	MP:0001926	female infertility	Insr<tm1Dac>/Insr<tm1Dac>,Tg(TTR-INSR)L2Dac/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	15254588
MGI:4831151	F	MP:0001926	female infertility	Insr<tm1Dac>/Insr<tm1Dac>,Tg(TTR-INSR)L3Dac/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	15254588
MGI:4834494	M	MP:0002169	no abnormal phenotype detected	Clcn5<tm4.1Tjj>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	20351103
MGI:4834495	F	MP:0005367	renal/urinary system phenotype	Clcn5<tm5.1Tjj>/Clcn5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	20351103
MGI:4834496	F	MP:0005367	renal/urinary system phenotype	Clcn3<tm1Tjj>/Clcn3<tm1Tjj>,Clcn5<tm5.1Tjj>/Clcn5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	20351103
MGI:4834498	F	MP:0005367	renal/urinary system phenotype	Clcn4<tm1Tjj>/Clcn4<tm1Tjj>,Clcn5<tm5.1Tjj>/Clcn5<+>	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6	Y	20351103
MGI:4834499	M	MP:0011445	abnormal renal protein reabsorption	Clcn3<tm1Tjj>/Clcn3<tm1Tjj>,Clcn5<tm6.1Tjj>/Y,Tg(Vil1-cre)20Syr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	20351103
MGI:4834500	M	MP:0011445	abnormal renal protein reabsorption	Clcn4<tm1Tjj>/Clcn4<tm1Tjj>,Clcn5<tm6.1Tjj>/Y,Tg(Vil1-cre)20Syr/0	involves: 129/Sv * C57BL/6 * DBA/2	N	20351103
MGI:4834525	M	MP:0002675	asthenozoospermia	Aspm<Gt(AJ0069)Wtsi>/Aspm<Gt(AJ0069)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834525	M	MP:0002687	oligozoospermia	Aspm<Gt(AJ0069)Wtsi>/Aspm<Gt(AJ0069)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834525	M	MP:0004852	decreased testis weight	Aspm<Gt(AJ0069)Wtsi>/Aspm<Gt(AJ0069)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834525	F	MP:0004856	decreased ovary weight	Aspm<Gt(AJ0069)Wtsi>/Aspm<Gt(AJ0069)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834525	M	MP:0001922	reduced male fertility	Aspm<Gt(AJ0069)Wtsi>/Aspm<Gt(AJ0069)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834525	F	MP:0001923	reduced female fertility	Aspm<Gt(AJ0069)Wtsi>/Aspm<Gt(AJ0069)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834525	M	MP:0009235	small sperm head	Aspm<Gt(AJ0069)Wtsi>/Aspm<Gt(AJ0069)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834526	M	MP:0002675	asthenozoospermia	Aspm<Gt(AA0137)Wtsi>/Aspm<Gt(AA0137)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834526	M	MP:0004852	decreased testis weight	Aspm<Gt(AA0137)Wtsi>/Aspm<Gt(AA0137)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834526	M	MP:0009235	small sperm head	Aspm<Gt(AA0137)Wtsi>/Aspm<Gt(AA0137)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834526	F	MP:0001923	reduced female fertility	Aspm<Gt(AA0137)Wtsi>/Aspm<Gt(AA0137)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834526	M	MP:0002687	oligozoospermia	Aspm<Gt(AA0137)Wtsi>/Aspm<Gt(AA0137)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834526	M	MP:0001922	reduced male fertility	Aspm<Gt(AA0137)Wtsi>/Aspm<Gt(AA0137)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834526	F	MP:0004856	decreased ovary weight	Aspm<Gt(AA0137)Wtsi>/Aspm<Gt(AA0137)Wtsi>	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	N	20823249
MGI:4834527	F	MP:0001386	abnormal maternal nurturing	Mbp<shi>/Mbp<shi>	SWV-Mbp<shi>	N	6168677
MGI:4834559	F	MP:0020938	decreased susceptibility to Picornaviridae infection	Plp1<jp-rsh>/Plp1<jp-rsh>	involves: 101/H * C3H	N	9188567
MGI:4834678	F	MP:0008779	abnormal maternal behavior	Dscam<del17>/Dscam<del17>	either: (involves: BALB/cByJ * C57BL/6J) or (involves: 129S1/SvImJ * BALB/cByJ * C57BL/6J)	N	20715164
MGI:4834679	F	MP:0009503	abnormal mammary gland duct morphology	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv	N	12810593
MGI:4834679	F	MP:0006269	abnormal mammary gland growth during pregnancy	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv	N	12810593
MGI:4834679	F	MP:0009506	abnormal mammary gland alveolus morphology	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv	N	12810593
MGI:4834679	F	MP:0001881	abnormal mammary gland physiology	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv	N	12810593
MGI:4834679	F	MP:0006271	abnormal involution of the mammary gland	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv	N	12810593
MGI:4834865	F	MP:0000628	abnormal mammary gland development	Tg(MMTV-PTGS2)#Thla/0	involves: 129S6/SvEvTac * C57BL/6 * CD-1 * FVB/N	N	15930264
MGI:4834865	F	MP:0000630	mammary gland hyperplasia	Tg(MMTV-PTGS2)#Thla/0	involves: 129S6/SvEvTac * C57BL/6 * CD-1 * FVB/N	N	15930264
MGI:4834866	F	MP:0000630	mammary gland hyperplasia	Tg(MMTV-PTGS2)#Thla/0	involves: CD-1	N	11278747
MGI:4834866	F	MP:0006271	abnormal involution of the mammary gland	Tg(MMTV-PTGS2)#Thla/0	involves: CD-1	N	11278747
MGI:4834890	F	MP:0002644	decreased circulating triglyceride level	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv * C57BL/6 * MF1	N	14741342
MGI:4834890	F	MP:0005669	increased circulating leptin level	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv * C57BL/6 * MF1	N	14741342
MGI:4835032	F	MP:0000008	increased white adipose tissue amount	Rai1<tm1Jrl>/Rai1<+>	B6.129S7-Rai1<tm1Jrl>/J	N	20663924
MGI:4835032	F	MP:0020411	increased abdominal adipose tissue amount	Rai1<tm1Jrl>/Rai1<+>	B6.129S7-Rai1<tm1Jrl>/J	N	20663924
MGI:4835048	M	MP:0014237	decreased tumor-free survival time	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,X/Tg(Tyr-HRAS)60Lc	involves: 129/Sv * C57BL/6J * CBA/J * SJL	N	20697345
MGI:4835048	M	MP:0010275	increased melanoma incidence	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,X/Tg(Tyr-HRAS)60Lc	involves: 129/Sv * C57BL/6J * CBA/J * SJL	N	20697345
MGI:4835048	M	MP:0003447	decreased tumor growth/size	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,X/Tg(Tyr-HRAS)60Lc	involves: 129/Sv * C57BL/6J * CBA/J * SJL	N	20697345
MGI:4835335	M	MP:0001405	impaired coordination	Plp1<tm1Gow>/Y	Not Specified	N	10818135
MGI:4835335	M	MP:0005405	axon degeneration	Plp1<tm1Gow>/Y	Not Specified	N	10818135
MGI:4835335	M	MP:0002229	neurodegeneration	Plp1<tm1Gow>/Y	Not Specified	N	10818135
MGI:4835335	M	MP:0000921	demyelination	Plp1<tm1Gow>/Y	Not Specified	N	10818135
MGI:4835335	M	MP:0009978	abnormal cerebellum white matter morphology	Plp1<tm1Gow>/Y	Not Specified	N	10818135
MGI:4835335	M	MP:0000920	abnormal myelination	Plp1<tm1Gow>/Y	Not Specified	N	10818135
MGI:4835335	M	MP:0010047	axonal spheroids	Plp1<tm1Gow>/Y	Not Specified	N	10818135
MGI:4835335	M	MP:0002183	gliosis	Plp1<tm1Gow>/Y	Not Specified	N	10818135
MGI:4835336	M	MP:0000886	abnormal cerebellar granule layer morphology	Plp1<tm1.1Gow>/Y	Not Specified	N	10818135
MGI:4835336	M	MP:0000849	abnormal cerebellum morphology	Plp1<tm1.1Gow>/Y	Not Specified	N	10818135
MGI:4835336	M	MP:0009978	abnormal cerebellum white matter morphology	Plp1<tm1.1Gow>/Y	Not Specified	N	10818135
MGI:4835336	M	MP:0002183	gliosis	Plp1<tm1.1Gow>/Y	Not Specified	N	10818135
MGI:4835336	M	MP:0010047	axonal spheroids	Plp1<tm1.1Gow>/Y	Not Specified	N	10818135
MGI:4835336	M	MP:0000921	demyelination	Plp1<tm1.1Gow>/Y	Not Specified	N	10818135
MGI:4835336	M	MP:0001405	impaired coordination	Plp1<tm1.1Gow>/Y	Not Specified	N	10818135
MGI:4835336	M	MP:0000920	abnormal myelination	Plp1<tm1.1Gow>/Y	Not Specified	N	10818135
MGI:4835336	M	MP:0005405	axon degeneration	Plp1<tm1.1Gow>/Y	Not Specified	N	10818135
MGI:4835336	M	MP:0002229	neurodegeneration	Plp1<tm1.1Gow>/Y	Not Specified	N	10818135
MGI:4835424	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm13(Ple54-EGFP)Ems>/Y	B6.129P2(Cg)-Hprt1<tm13(Ple54-EGFP)Ems>/Mmjax	N	MGI:3835781
MGI:4835425	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm14(Ple103-EGFP/cre)Ems>/Y	B6.129P2(129S4)-Hprt1<tm14(Ple103-EGFP/cre)Ems>	N	MGI:3835781
MGI:4835426	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm15(Ple111-EGFP)Ems>/Y	B6.129P2(Cg)-Hprt1<tm15(Ple111-EGFP)Ems>/Mmjax	N	MGI:3835781
MGI:4835432	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm16(Ple167-EGFP/cre)Ems>/Y	B6.129P2(129S4)-Hprt1<tm16(Ple167-EGFP/cre)Ems>	N	MGI:3835781
MGI:4835433	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm18(Ple90-EGFP)Ems>/Y	B6.129P2(Cg)-Hprt1<tm18(Ple90-EGFP)Ems>/Mmjax	N	MGI:3835781
MGI:4835434	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm17(Ple48-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm17(Ple48-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835435	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm31(Ple67-EGFP)Ems>/Y	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	MGI:3835781
MGI:4835436	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm20(Ple53-EGFP)Ems>/Y	B6.129P2(Cg)-Hprt1<tm20(Ple53-EGFP)Ems>/Mmjax	N	MGI:3835781
MGI:4835437	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm32(Ple112-EGFP)Ems>/Y	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	MGI:3835781
MGI:4835438	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm33(Ple183-EGFP)Ems>/Y	B6.129P2(Cg)-Hprt1<tm33(Ple183-EGFP)Ems>/Mmjax	N	MGI:3835781
MGI:4835448	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm37(lacZ)Ems>/Y	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	MGI:3835781
MGI:4835450	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm44(Ple49-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm44(Ple49-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835451	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm34(Ple186-EGFP)Ems>/Y	B6.129P2(Cg)-Hprt1<tm34(Ple186-EGFP)Ems>/Mmjax	N	MGI:3835781
MGI:4835452	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm54(Ple233-EGFP)Ems>/Y	B6.129P2(Cg)-Hprt1<tm54(Ple233-EGFP)Ems>/Mmjax	N	MGI:3835781
MGI:4835453	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm41(Ple160-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm41(Ple160-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835455	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm42(Ple131-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm42(Ple131-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835456	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm45(Ple67-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm45(Ple67-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835457	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm50(Ple55-lacZ)Ems>/Y	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	MGI:3835781
MGI:4835458	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm63(Ple12-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm63(Ple12-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835459	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm64(Ple170-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm64(Ple170-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835460	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm65(Ple53-lacZ)Ems>/Y	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	MGI:3835781
MGI:4835461	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm66(Ple5-lacZ)Ems>/Y	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	MGI:3835781
MGI:4835463	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm19(Ple88-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm19(Ple88-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835464	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm38(Ple17-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm38(Ple17-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835465	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm39(Ple24-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm39(Ple24-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835466	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm40(Ple34-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm40(Ple34-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835471	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm43(Ple140-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm43(Ple140-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835472	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm56(Ple25-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm56(Ple25-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835474	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm58(Ple119-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm58(Ple119-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835475	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm59(Ple123-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm59(Ple123-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835476	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm62(Ple153-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm62(Ple153-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835478	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm67(Ple238-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm67(Ple238-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835480	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm68(Ple127-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm68(Ple127-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835481	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm69(Ple134-lacZ)Ems>/Y	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	MGI:3835781
MGI:4835483	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm70(Ple240-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm70(Ple240-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835485	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm71(Ple155-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm71(Ple155-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835486	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm72(Ple158-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm72(Ple158-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835487	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm73(Ple142-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm73(Ple142-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835488	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm53(CAG-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm53(CAG-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835489	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm74(Ple232-lacZ)Ems>/Y	B6.129P2(Cg)-Hprt1<tm74(Ple232-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:4835907	F	MP:0001923	reduced female fertility	Clcn1<adr>/Clcn1<adr>	A2G-Clcn1<adr>	N	10628777
MGI:4835907	M	MP:0001925	male infertility	Clcn1<adr>/Clcn1<adr>	A2G-Clcn1<adr>	N	10628777
MGI:4836055	M	MP:0011085	postnatal lethality, complete penetrance	Atp6ap2<tm1.1Aich>/Y,Tg(Myh6-cre)2182Mds/?	involves: C57BL/6 * FVB/N	N	20570919
MGI:4836055	M	MP:0001544	abnormal cardiovascular system physiology	Atp6ap2<tm1.1Aich>/Y,Tg(Myh6-cre)2182Mds/?	involves: C57BL/6 * FVB/N	N	20570919
MGI:4836055	M	MP:0005598	decreased heart ventricle muscle contractility	Atp6ap2<tm1.1Aich>/Y,Tg(Myh6-cre)2182Mds/?	involves: C57BL/6 * FVB/N	N	20570919
MGI:4836055	M	MP:0000266	abnormal heart morphology	Atp6ap2<tm1.1Aich>/Y,Tg(Myh6-cre)2182Mds/?	involves: C57BL/6 * FVB/N	N	20570919
MGI:4836055	M	MP:0004857	abnormal heart weight	Atp6ap2<tm1.1Aich>/Y,Tg(Myh6-cre)2182Mds/?	involves: C57BL/6 * FVB/N	N	20570919
MGI:4836171	F	MP:0002682	decreased mature ovarian follicle number	Smc1b<m1Ham>/Smc1b<m1Ham>	involves: C57BL/6JJcl * DBA/2JJcl * ICR	N	19491376
MGI:4836171	M	MP:0001925	male infertility	Smc1b<m1Ham>/Smc1b<m1Ham>	involves: C57BL/6JJcl * DBA/2JJcl * ICR	N	19491376
MGI:4836171	M	MP:0004852	decreased testis weight	Smc1b<m1Ham>/Smc1b<m1Ham>	involves: C57BL/6JJcl * DBA/2JJcl * ICR	N	19491376
MGI:4836171	M	MP:0008280	abnormal male germ cell apoptosis	Smc1b<m1Ham>/Smc1b<m1Ham>	involves: C57BL/6JJcl * DBA/2JJcl * ICR	N	19491376
MGI:4836171	M	MP:0005159	azoospermia	Smc1b<m1Ham>/Smc1b<m1Ham>	involves: C57BL/6JJcl * DBA/2JJcl * ICR	N	19491376
MGI:4836171	F	MP:0001926	female infertility	Smc1b<m1Ham>/Smc1b<m1Ham>	involves: C57BL/6JJcl * DBA/2JJcl * ICR	N	19491376
MGI:4836241	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(Pbsn-TAg)15Tvd/0	involves: C57BL/6 * DBA/2	N	16288012
MGI:4836241	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-TAg)15Tvd/0	involves: C57BL/6 * DBA/2	N	16288012
MGI:4836241	M	MP:0001167	prostate gland epithelial hyperplasia	Tg(Pbsn-TAg)15Tvd/0	involves: C57BL/6 * DBA/2	N	16288012
MGI:4836241	M	MP:0001168	abnormal prostate gland epithelium morphology	Tg(Pbsn-TAg)15Tvd/0	involves: C57BL/6 * DBA/2	N	16288012
MGI:4836241	M	MP:0001925	male infertility	Tg(Pbsn-TAg)15Tvd/0	involves: C57BL/6 * DBA/2	N	16288012
MGI:4836242	M	MP:0001168	abnormal prostate gland epithelium morphology	Tg(Pbsn-TAg)15Tvd/0,Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * C57BL/6 * DBA/2	N	16288012
MGI:4836243	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Ppp>/Pten<+>,Tg(Pbsn-TAg)15Tvd/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	16288012
MGI:4836243	M	MP:0003607	abnormal prostate gland physiology	Pten<tm1Ppp>/Pten<+>,Tg(Pbsn-TAg)15Tvd/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	16288012
MGI:4836243	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Ppp>/Pten<+>,Tg(Pbsn-TAg)15Tvd/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	16288012
MGI:4836243	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm1Ppp>/Pten<+>,Tg(Pbsn-TAg)15Tvd/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	16288012
MGI:4836591	F	MP:0001126	abnormal ovary morphology	Kras<tm4Tyj>/Kras<+>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C3H/HeJ)	N	15619626
MGI:4836596	F	MP:0004868	increased endometrial carcinoma incidence	Kras<tm4Tyj>/Kras<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * C57BL/6J	N	15619626
MGI:4836749	M	MP:0011091	prenatal lethality, complete penetrance	Tfpi<tm1.1Rdsi>/Tfpi<tm1.1Rdsi>,Tg(CMV-cre)1Cgn/Y	involves: 129S4/SvJaeSor * 129S6/SvEvTac * BALB/cJ * C57BL/6	N	20516367
MGI:4836911	M	MP:0001925	male infertility	Dnd1<Ter>/Dnd1<Ter>,Sf1<Gt(XD130)Byg>/Sf1<+>	involves: 129P2/OlaHsd * 129S1/SvImJ * 129T1/Sv	N	20736371
MGI:4836911	M	MP:0006262	increased testis tumor incidence	Dnd1<Ter>/Dnd1<Ter>,Sf1<Gt(XD130)Byg>/Sf1<+>	involves: 129P2/OlaHsd * 129S1/SvImJ * 129T1/Sv	N	20736371
MGI:4836911	M	MP:0001147	small testis	Dnd1<Ter>/Dnd1<Ter>,Sf1<Gt(XD130)Byg>/Sf1<+>	involves: 129P2/OlaHsd * 129S1/SvImJ * 129T1/Sv	N	20736371
MGI:4836912	M	MP:0006262	increased testis tumor incidence	Sf1<Gt(XD130)Byg>/Sf1<+>	involves: 129P2/OlaHsd * 129S1/SvImJ * MOLF/Ei	N	20736371
MGI:4836991	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm57(Ple26-lacZ)Ems>/Y	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	MGI:3835781
MGI:4837000	F	MP:0001926	female infertility	Bmpr1b<Tn(sb-lacZ,GFP)IR3.PV50Jtak>/Bmpr1b<Tn(sb-lacZ,GFP)IR3.PV50Jtak>	involves: C3H * C57BL/6 * DBA/2 * ICR	N	16179923
MGI:4837215	M	MP:0001925	male infertility	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>	B6.129-Paip2<tm1.2Nso>	N	20739757
MGI:4837215	M	MP:0002662	abnormal cauda epididymis morphology	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>	B6.129-Paip2<tm1.2Nso>	N	20739757
MGI:4837220	M	MP:0004929	decreased epididymis weight	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>,Paip2b<tm1.2Nso>/Paip2b<tm1.2Nso>	B6.129-Paip2b<tm1.2Nso> Paip2<tm1.2Nso>	N	20739757
MGI:4837220	M	MP:0009231	detached acrosome	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>,Paip2b<tm1.2Nso>/Paip2b<tm1.2Nso>	B6.129-Paip2b<tm1.2Nso> Paip2<tm1.2Nso>	N	20739757
MGI:4837220	M	MP:0002662	abnormal cauda epididymis morphology	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>,Paip2b<tm1.2Nso>/Paip2b<tm1.2Nso>	B6.129-Paip2b<tm1.2Nso> Paip2<tm1.2Nso>	N	20739757
MGI:4837220	M	MP:0009232	abnormal sperm nucleus morphology	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>,Paip2b<tm1.2Nso>/Paip2b<tm1.2Nso>	B6.129-Paip2b<tm1.2Nso> Paip2<tm1.2Nso>	N	20739757
MGI:4837220	M	MP:0005159	azoospermia	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>,Paip2b<tm1.2Nso>/Paip2b<tm1.2Nso>	B6.129-Paip2b<tm1.2Nso> Paip2<tm1.2Nso>	N	20739757
MGI:4837220	M	MP:0006380	abnormal spermatid morphology	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>,Paip2b<tm1.2Nso>/Paip2b<tm1.2Nso>	B6.129-Paip2b<tm1.2Nso> Paip2<tm1.2Nso>	N	20739757
MGI:4837220	M	MP:0004901	decreased male germ cell number	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>,Paip2b<tm1.2Nso>/Paip2b<tm1.2Nso>	B6.129-Paip2b<tm1.2Nso> Paip2<tm1.2Nso>	N	20739757
MGI:4837220	M	MP:0001925	male infertility	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>,Paip2b<tm1.2Nso>/Paip2b<tm1.2Nso>	B6.129-Paip2b<tm1.2Nso> Paip2<tm1.2Nso>	N	20739757
MGI:4837220	M	MP:0004962	decreased prostate gland weight	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>,Paip2b<tm1.2Nso>/Paip2b<tm1.2Nso>	B6.129-Paip2b<tm1.2Nso> Paip2<tm1.2Nso>	N	20739757
MGI:4837220	M	MP:0001932	abnormal spermiogenesis	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>,Paip2b<tm1.2Nso>/Paip2b<tm1.2Nso>	B6.129-Paip2b<tm1.2Nso> Paip2<tm1.2Nso>	N	20739757
MGI:4837220	M	MP:0009833	absent sperm mitochondrial sheath	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>,Paip2b<tm1.2Nso>/Paip2b<tm1.2Nso>	B6.129-Paip2b<tm1.2Nso> Paip2<tm1.2Nso>	N	20739757
MGI:4837220	M	MP:0005578	teratozoospermia	Paip2<tm1.2Nso>/Paip2<tm1.2Nso>,Paip2b<tm1.2Nso>/Paip2b<tm1.2Nso>	B6.129-Paip2b<tm1.2Nso> Paip2<tm1.2Nso>	N	20739757
MGI:4837536	F	MP:0008705	increased interleukin-6 secretion	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0008500	increased IgG2a level	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0008617	increased circulating interleukin-12 level	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0004794	increased anti-nuclear antigen antibody level	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0008168	decreased B-1a cell number	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0004952	increased spleen weight	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0020519	renal glomerular immunoglobulin deposits	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0000691	enlarged spleen	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0008170	decreased B-1b cell number	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0008495	decreased IgG1 level	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0002743	glomerulonephritis	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0008206	increased B-2 B cell number	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0002494	increased IgM level	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0002493	increased IgG level	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0008127	decreased dendritic cell number	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0008182	decreased marginal zone B cell number	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0002362	abnormal spleen marginal zone morphology	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837536	F	MP:0004762	increased anti-double stranded DNA antibody level	Tlr8<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.129S1-Tlr8<tm1Vlcg>	N	20811154
MGI:4837537	F	MP:0002870	decreased anti-insulin autoantibody level	Tlr7<tm1Flv>/Tlr7<tm1Flv>	B6.129S1-Tlr7<tm1Flv>	N	20811154
MGI:4837537	F	MP:0001806	decreased IgM level	Tlr7<tm1Flv>/Tlr7<tm1Flv>	B6.129S1-Tlr7<tm1Flv>	N	20811154
MGI:4837537	F	MP:0008496	decreased IgG2a level	Tlr7<tm1Flv>/Tlr7<tm1Flv>	B6.129S1-Tlr7<tm1Flv>	N	20811154
MGI:4837537	F	MP:0001805	decreased IgG level	Tlr7<tm1Flv>/Tlr7<tm1Flv>	B6.129S1-Tlr7<tm1Flv>	N	20811154
MGI:4837537	F	MP:0008495	decreased IgG1 level	Tlr7<tm1Flv>/Tlr7<tm1Flv>	B6.129S1-Tlr7<tm1Flv>	N	20811154
MGI:4837538	F	MP:0008181	increased marginal zone B cell number	Tlr8/Tlr7<tm1Vlcg>/Tlr8/Tlr7<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg> Tlr8<tm1Vlcg>	N	20811154
MGI:4837538	F	MP:0008174	decreased follicular B cell number	Tlr8/Tlr7<tm1Vlcg>/Tlr8/Tlr7<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg> Tlr8<tm1Vlcg>	N	20811154
MGI:4837538	F	MP:0002870	decreased anti-insulin autoantibody level	Tlr8/Tlr7<tm1Vlcg>/Tlr8/Tlr7<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg> Tlr8<tm1Vlcg>	N	20811154
MGI:4837539	F	MP:0002493	increased IgG level	Tlr8/Tlr7<tm1Vlcg>/Tlr7<+>,Tlr8/Tlr7<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg> Tlr8<tm1Vlcg>	N	20811154
MGI:4837539	F	MP:0002870	decreased anti-insulin autoantibody level	Tlr8/Tlr7<tm1Vlcg>/Tlr7<+>,Tlr8/Tlr7<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg> Tlr8<tm1Vlcg>	N	20811154
MGI:4837539	F	MP:0008181	increased marginal zone B cell number	Tlr8/Tlr7<tm1Vlcg>/Tlr7<+>,Tlr8/Tlr7<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg> Tlr8<tm1Vlcg>	N	20811154
MGI:4837539	F	MP:0001806	decreased IgM level	Tlr8/Tlr7<tm1Vlcg>/Tlr7<+>,Tlr8/Tlr7<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg> Tlr8<tm1Vlcg>	N	20811154
MGI:4837539	F	MP:0001805	decreased IgG level	Tlr8/Tlr7<tm1Vlcg>/Tlr7<+>,Tlr8/Tlr7<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg> Tlr8<tm1Vlcg>	N	20811154
MGI:4837539	F	MP:0002362	abnormal spleen marginal zone morphology	Tlr8/Tlr7<tm1Vlcg>/Tlr7<+>,Tlr8/Tlr7<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg> Tlr8<tm1Vlcg>	N	20811154
MGI:4837539	F	MP:0008182	decreased marginal zone B cell number	Tlr8/Tlr7<tm1Vlcg>/Tlr7<+>,Tlr8/Tlr7<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg> Tlr8<tm1Vlcg>	N	20811154
MGI:4837539	F	MP:0002494	increased IgM level	Tlr8/Tlr7<tm1Vlcg>/Tlr7<+>,Tlr8/Tlr7<tm1Vlcg>/Tlr8<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg> Tlr8<tm1Vlcg>	N	20811154
MGI:4837845	F	MP:0002870	decreased anti-insulin autoantibody level	Tlr8/Tlr7<tm1Vlcg>/Tlr8/Tlr7<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg>	N	20811154
MGI:4837845	F	MP:0008174	decreased follicular B cell number	Tlr8/Tlr7<tm1Vlcg>/Tlr8/Tlr7<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg>	N	20811154
MGI:4837845	F	MP:0008181	increased marginal zone B cell number	Tlr8/Tlr7<tm1Vlcg>/Tlr8/Tlr7<tm1Vlcg>	B6.Cg-Tlr8/Tlr7<tm1Vlcg>	N	20811154
MGI:4837857	F	MP:0001881	abnormal mammary gland physiology	Nos2<tm1Mrl>/Nos2<tm1Mrl>	B6.129S7-Nos2<tm1Mrl>	N	20345368
MGI:4837857	F	MP:0013717	hyperlactation	Nos2<tm1Mrl>/Nos2<tm1Mrl>	B6.129S7-Nos2<tm1Mrl>	N	20345368
MGI:4837857	F	MP:0006271	abnormal involution of the mammary gland	Nos2<tm1Mrl>/Nos2<tm1Mrl>	B6.129S7-Nos2<tm1Mrl>	N	20345368
MGI:4838048	M	MP:0001147	small testis	Sh2d3c<tm1.1Ebp>/Sh2d3c<tm1.1Ebp>	involves: C57BL/6	N	20881139
MGI:4838146	F	MP:0005168	abnormal female meiosis	Npr2<cn-2J>/Npr2<cn-2J>	B6;CBACa A<w-J>/A-Npr2<cn-2J>/GrsrJ	N	20947764
MGI:4838162	F	MP:0002086	abnormal extraembryonic tissue morphology	Rlim<tm1.1Inba>/Rlim<tm1.2Inba>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB	N	20962847
MGI:4838162	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Rlim<tm1.1Inba>/Rlim<tm1.2Inba>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB	N	20962847
MGI:4838162	F	MP:0004179	transmission ratio distortion	Rlim<tm1.1Inba>/Rlim<tm1.2Inba>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB	N	20962847
MGI:4838162	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Rlim<tm1.1Inba>/Rlim<tm1.2Inba>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB	N	20962847
MGI:4838162	F	MP:0001672	abnormal embryo development	Rlim<tm1.1Inba>/Rlim<tm1.2Inba>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB	N	20962847
MGI:4838163	F	MP:0010768	mortality/aging	Rlim<tm1.1Inba>/Rlim<tm1.1Inba>,Tg(MMTV-cre)4Mam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB	Y	20962847
MGI:4838164	M	MP:0002169	no abnormal phenotype detected	Rlim<tm1.2Inba>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB	N	20962847
MGI:4838185	F	MP:0004856	decreased ovary weight	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Wnt4<tm1.1Boer>/Wnt4<tm1.2Boer>	involves: 129S1/Sv * 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ	N	20371632
MGI:4838185	F	MP:0002682	decreased mature ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Wnt4<tm1.1Boer>/Wnt4<tm1.2Boer>	involves: 129S1/Sv * 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ	N	20371632
MGI:4838185	F	MP:0003582	abnormal ovary development	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Wnt4<tm1.1Boer>/Wnt4<tm1.2Boer>	involves: 129S1/Sv * 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ	N	20371632
MGI:4838205	F	MP:0001382	abnormal nursing	Tg(Eno2-TOR1A*)13Shas/0	involves: C3H * C57BL/6J	N	15548549
MGI:4838262	F	MP:0006269	abnormal mammary gland growth during pregnancy	Il4/Il13<tm3Anjm>/Il4/Il13<tm3Anjm>	involves: 129P2/OlaHsd * BALB/c	N	17611223
MGI:4838263	F	MP:0006269	abnormal mammary gland growth during pregnancy	Il4/Il13<tm3Anjm>/Il4/Il13<tm3Anjm>	involves: 129P2/OlaHsd * BALB/c	N	17611223
MGI:4838299	F	MP:0001926	female infertility	Cdc20<Gt(XE368)Byg>/Cdc20<tm1Jvd>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	N	20941357
MGI:4838299	F	MP:0001125	abnormal oocyte morphology	Cdc20<Gt(XE368)Byg>/Cdc20<tm1Jvd>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	N	20941357
MGI:4838299	F	MP:0001923	reduced female fertility	Cdc20<Gt(XE368)Byg>/Cdc20<tm1Jvd>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	N	20941357
MGI:4838299	F	MP:0005168	abnormal female meiosis	Cdc20<Gt(XE368)Byg>/Cdc20<tm1Jvd>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	N	20941357
MGI:4838299	M	MP:0006362	abnormal male germ cell morphology	Cdc20<Gt(XE368)Byg>/Cdc20<tm1Jvd>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	N	20941357
MGI:4838303	M	MP:0004543	abnormal sperm physiology	Spesp1<tm1Osb>/Spesp1<tm1Osb>	involves: 129S2/SvPas * C57BL/6	N	20375058
MGI:4838303	M	MP:0008898	abnormal acrosome morphology	Spesp1<tm1Osb>/Spesp1<tm1Osb>	involves: 129S2/SvPas * C57BL/6	N	20375058
MGI:4838304	M	MP:0004543	abnormal sperm physiology	Spesp1<tm1Osb>/Spesp1<+>	involves: 129S2/SvPas * C57BL/6	N	20375058
MGI:4838305	F	MP:0002472	impaired complement alternative pathway	Cfp<tm2.1Song>/Cfp<tm2.1Song>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129 * C57BL/6 * FVB/N * SJL	N	20941861
MGI:4838306	F	MP:0003436	decreased susceptibility to induced arthritis	Cfp<tm2.1Song>/Cfp<tm2.1Song>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	involves: 129 * 129P2/OlaHsd * C57BL/6 * SJL	N	20941861
MGI:4838306	F	MP:0002472	impaired complement alternative pathway	Cfp<tm2.1Song>/Cfp<tm2.1Song>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	involves: 129 * 129P2/OlaHsd * C57BL/6 * SJL	N	20941861
MGI:4838307	F	MP:0002472	impaired complement alternative pathway	Cfp<tm1Song>/Cfp<tm1Song>	involves: 129 * C57BL/6	N	20941861
MGI:4838307	F	MP:0003436	decreased susceptibility to induced arthritis	Cfp<tm1Song>/Cfp<tm1Song>	involves: 129 * C57BL/6	N	20941861
MGI:4838308	F	MP:0010768	mortality/aging	Cfp<tm1Song>/Cfp<tm1Song>,Cr1l<tm1Hmo>/Cr1l<tm1Hmo>	involves: 129 * 129X1/SvJ * C57BL/6	Y	20941861
MGI:4838437	M	MP:0002687	oligozoospermia	Elmo1<tm1.1Ravi>/Elmo1<tm1.1Ravi>,Tg(Amh-cre)8815Reb/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	20844538
MGI:4838437	M	MP:0014052	increased male germ cell apoptosis	Elmo1<tm1.1Ravi>/Elmo1<tm1.1Ravi>,Tg(Amh-cre)8815Reb/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	20844538
MGI:4838437	M	MP:0002216	abnormal seminiferous tubule morphology	Elmo1<tm1.1Ravi>/Elmo1<tm1.1Ravi>,Tg(Amh-cre)8815Reb/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	20844538
MGI:4838438	M	MP:0008280	abnormal male germ cell apoptosis	Elmo1<tm1.2Ravi>/Elmo1<tm1.2Ravi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20844538
MGI:4838438	M	MP:0002216	abnormal seminiferous tubule morphology	Elmo1<tm1.2Ravi>/Elmo1<tm1.2Ravi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20844538
MGI:4838438	M	MP:0009853	decreased Sertoli cell phagocytosis	Elmo1<tm1.2Ravi>/Elmo1<tm1.2Ravi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20844538
MGI:4838438	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Elmo1<tm1.2Ravi>/Elmo1<tm1.2Ravi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20844538
MGI:4838438	M	MP:0002784	abnormal Sertoli cell morphology	Elmo1<tm1.2Ravi>/Elmo1<tm1.2Ravi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20844538
MGI:4838438	M	MP:0001146	abnormal testis morphology	Elmo1<tm1.2Ravi>/Elmo1<tm1.2Ravi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20844538
MGI:4838438	M	MP:0020550	multinucleated giant male germ cells	Elmo1<tm1.2Ravi>/Elmo1<tm1.2Ravi>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	20844538
MGI:4838529	M	MP:0009828	increased tumor latency	Akt2<tm1.1Mbb>/Akt2<tm1.1Mbb>,Pten<tm1Hwu>/Pten<tm1Hwu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA	N	20837017
MGI:4838529	M	MP:0002310	decreased susceptibility to hepatic steatosis	Akt2<tm1.1Mbb>/Akt2<tm1.1Mbb>,Pten<tm1Hwu>/Pten<tm1Hwu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA	N	20837017
MGI:4838529	M	MP:0000598	abnormal liver morphology	Akt2<tm1.1Mbb>/Akt2<tm1.1Mbb>,Pten<tm1Hwu>/Pten<tm1Hwu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA	N	20837017
MGI:4838532	M	MP:0000659	prostate gland hyperplasia	Tg(ARR2/Pbsn-FGF8)3Prb/0	involves: C57BL/6 * DBA/2	N	16489020
MGI:4838532	M	MP:0000659	prostate gland hyperplasia	Tg(ARR2/Pbsn-FGF8)3Prb/0	involves: C57BL/6 * DBA/2	N	12208767
MGI:4838532	M	MP:0001158	abnormal prostate gland morphology	Tg(ARR2/Pbsn-FGF8)3Prb/0	involves: C57BL/6 * DBA/2	N	12208767
MGI:4838532	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(ARR2/Pbsn-FGF8)3Prb/0	involves: C57BL/6 * DBA/2	N	12208767
MGI:4838532	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(ARR2/Pbsn-FGF8)3Prb/0	involves: C57BL/6 * DBA/2	N	16489020
MGI:4838532	M	MP:0003608	prostate gland inflammation	Tg(ARR2/Pbsn-FGF8)3Prb/0	involves: C57BL/6 * DBA/2	N	12208767
MGI:4839039	M	MP:0001823	thymus hypoplasia	Nkap<tm1.1Viss>/Y,Tg(Lck-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ	N	19409814
MGI:4839039	M	MP:0005092	decreased double-positive T cell number	Nkap<tm1.1Viss>/Y,Tg(Lck-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ	N	19409814
MGI:4839039	M	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Nkap<tm1.1Viss>/Y,Tg(Lck-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ	N	19409814
MGI:4839039	M	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Nkap<tm1.1Viss>/Y,Tg(Lck-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ	N	19409814
MGI:4839039	M	MP:0010136	decreased DN4 thymocyte number	Nkap<tm1.1Viss>/Y,Tg(Lck-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ	N	19409814
MGI:4839039	M	MP:0000715	decreased thymocyte number	Nkap<tm1.1Viss>/Y,Tg(Lck-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ	N	19409814
MGI:4839039	M	MP:0010133	increased DN3 thymocyte number	Nkap<tm1.1Viss>/Y,Tg(Lck-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ	N	19409814
MGI:4839039	M	MP:0001825	arrested T cell differentiation	Nkap<tm1.1Viss>/Y,Tg(Lck-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ	N	19409814
MGI:4839056	F	MP:0008054	abnormal uterine NK cell morphology	Ifng<tm1Ts>/Ifng<tm1Ts>	C.129S7(B6)-Ifng<tm1Ts>/J	N	10411532
MGI:4839056	F	MP:0009394	increased uterine NK cell number	Ifng<tm1Ts>/Ifng<tm1Ts>	C.129S7(B6)-Ifng<tm1Ts>/J	N	10411532
MGI:4839056	F	MP:0004256	abnormal maternal decidual layer morphology	Ifng<tm1Ts>/Ifng<tm1Ts>	C.129S7(B6)-Ifng<tm1Ts>/J	N	10411532
MGI:4839056	F	MP:0009099	abnormal uterine NK cell physiology	Ifng<tm1Ts>/Ifng<tm1Ts>	C.129S7(B6)-Ifng<tm1Ts>/J	N	10411532
MGI:4839101	M	MP:0030978	impaired binding of sperm to zona pellucida	Zan<tm1Dmh>/Zan<tm1Dmh>	B6.129-Zan<tm1Dmh>	N	20529856
MGI:4839213	F	MP:0001125	abnormal oocyte morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Gdf9-icre)5092Coo/0	B6.Cg-Pten<tm1Hwu> Tg(Gdf9-icre)5092Coo	N	18239123
MGI:4839213	F	MP:0009361	abnormal primordial ovarian follicle morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Gdf9-icre)5092Coo/0	B6.Cg-Pten<tm1Hwu> Tg(Gdf9-icre)5092Coo	N	18239123
MGI:4839213	F	MP:0001131	abnormal ovarian follicle morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Gdf9-icre)5092Coo/0	B6.Cg-Pten<tm1Hwu> Tg(Gdf9-icre)5092Coo	N	18239123
MGI:4839213	F	MP:0001130	abnormal ovarian folliculogenesis	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Gdf9-icre)5092Coo/0	B6.Cg-Pten<tm1Hwu> Tg(Gdf9-icre)5092Coo	N	18239123
MGI:4839213	F	MP:0031020	premature ovarian failure	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Gdf9-icre)5092Coo/0	B6.Cg-Pten<tm1Hwu> Tg(Gdf9-icre)5092Coo	N	18239123
MGI:4839213	F	MP:0001926	female infertility	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Gdf9-icre)5092Coo/0	B6.Cg-Pten<tm1Hwu> Tg(Gdf9-icre)5092Coo	N	18239123
MGI:4839213	F	MP:0011121	decreased primordial ovarian follicle number	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Gdf9-icre)5092Coo/0	B6.Cg-Pten<tm1Hwu> Tg(Gdf9-icre)5092Coo	N	18239123
MGI:4839213	F	MP:0001927	abnormal estrous cycle	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Gdf9-icre)5092Coo/0	B6.Cg-Pten<tm1Hwu> Tg(Gdf9-icre)5092Coo	N	18239123
MGI:4839213	F	MP:0011122	absent primordial ovarian follicles	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Gdf9-icre)5092Coo/0	B6.Cg-Pten<tm1Hwu> Tg(Gdf9-icre)5092Coo	N	18239123
MGI:4839213	F	MP:0004832	enlarged ovary	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Gdf9-icre)5092Coo/0	B6.Cg-Pten<tm1Hwu> Tg(Gdf9-icre)5092Coo	N	18239123
MGI:4839213	F	MP:0002679	abnormal corpus luteum morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Gdf9-icre)5092Coo/0	B6.Cg-Pten<tm1Hwu> Tg(Gdf9-icre)5092Coo	N	18239123
MGI:4839333	M	MP:0005389	reproductive system phenotype	X/Sry<AKR/J> Sry<RIII>	C57BL/6JEi-Chr Y<AKR-Sxr>/EiJ	Y	12750339
MGI:4839497	F	MP:0001138	abnormal uterine cervix squamous epithelium morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Vhl<tm1Jae>/Vhl<tm1Jae>,Tg(Cdh16-cre)91Igr/0	involves: 129S4/SvJae * ICR	N	18474617
MGI:4839497	F	MP:0009092	endometrium hyperplasia	Pten<tm1Hwu>/Pten<tm1Hwu>,Vhl<tm1Jae>/Vhl<tm1Jae>,Tg(Cdh16-cre)91Igr/0	involves: 129S4/SvJae * ICR	N	18474617
MGI:4839497	F	MP:0003574	abnormal oviduct morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Vhl<tm1Jae>/Vhl<tm1Jae>,Tg(Cdh16-cre)91Igr/0	involves: 129S4/SvJae * ICR	N	18474617
MGI:4839497	M	MP:0002631	abnormal epididymis morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Vhl<tm1Jae>/Vhl<tm1Jae>,Tg(Cdh16-cre)91Igr/0	involves: 129S4/SvJae * ICR	N	18474617
MGI:4839497	M	MP:0003597	increased epididymal cystadenoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Vhl<tm1Jae>/Vhl<tm1Jae>,Tg(Cdh16-cre)91Igr/0	involves: 129S4/SvJae * ICR	N	18474617
MGI:4839498	M	MP:0002631	abnormal epididymis morphology	Vhl<tm1Jae>/Vhl<tm1Jae>,Tg(Cdh16-cre)91Igr/0	involves: 129S4/SvJae * ICR	N	18474617
MGI:4839499	M	MP:0002769	abnormal vas deferens morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Cdh16-cre)91Igr/0	involves: 129S4/SvJae * ICR	N	18474617
MGI:4839499	M	MP:0004933	abnormal epididymis epithelium morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Cdh16-cre)91Igr/0	involves: 129S4/SvJae * ICR	N	18474617
MGI:4839499	M	MP:0002059	abnormal seminal vesicle morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Cdh16-cre)91Igr/0	involves: 129S4/SvJae * ICR	N	18474617
MGI:4839499	F	MP:0009092	endometrium hyperplasia	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Cdh16-cre)91Igr/0	involves: 129S4/SvJae * ICR	N	18474617
MGI:4839499	F	MP:0004896	abnormal endometrium morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Cdh16-cre)91Igr/0	involves: 129S4/SvJae * ICR	N	18474617
MGI:4839513	M	MP:0002950	abnormal neural crest cell migration	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0011732	decreased somite size	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0002884	abnormal pharyngeal arch morphology	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0011092	embryonic lethality, complete penetrance	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0011260	abnormal head mesenchyme morphology	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0000267	abnormal heart development	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0002151	abnormal neural tube morphology	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0001691	abnormal somite shape	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0010642	absent third pharyngeal arch	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0004251	failure of heart looping	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0001688	abnormal somite development	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0004073	caudal body truncation	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0003400	kinked neural tube	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0006337	abnormal first pharyngeal arch morphology	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0006345	absent second pharyngeal arch	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0005223	abnormal dorsal-ventral polarity of the somites	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839513	M	MP:0000929	open neural tube	Med12<tm1Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839514	M	MP:0002169	no abnormal phenotype detected	Med12<tm1.1Hsch>/Y	involves: 129S6/SvEvTac * C57BL/6NCrl	N	20630950
MGI:4839515	F	MP:0002169	no abnormal phenotype detected	Med12<tm1.1Hsch>/Med12<tm1.1Hsch>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	20630950
MGI:4839516	M	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance	Med12<tm1.2Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839516	M	MP:0012159	absent anterior visceral endoderm	Med12<tm1.2Hsch>/Y	chimera involves: 129S6/SvEvTac * C57BL/6NCr	N	20630950
MGI:4839546	M	MP:0001922	reduced male fertility	stm/stm	involves: CBA/FaCam	N	641946
MGI:4839546	F	MP:0001923	reduced female fertility	stm/stm	involves: CBA/FaCam	N	641946
MGI:4839553	F	MP:0003051	curly tail	Med12<tm1.1Hsch>/Med12<+>,Tg(CMV-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6	N	20589884
MGI:4839553	F	MP:0002151	abnormal neural tube morphology	Med12<tm1.1Hsch>/Med12<+>,Tg(CMV-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6	N	20589884
MGI:4839553	F	MP:0000914	exencephaly	Med12<tm1.1Hsch>/Med12<+>,Tg(CMV-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6	N	20589884
MGI:4839553	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Med12<tm1.1Hsch>/Med12<+>,Tg(CMV-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6	N	20589884
MGI:4839553	F	MP:0011101	prenatal lethality, incomplete penetrance	Med12<tm1.1Hsch>/Med12<+>,Tg(CMV-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6	N	20589884
MGI:4839553	F	MP:0000074	abnormal neurocranium morphology	Med12<tm1.1Hsch>/Med12<+>,Tg(CMV-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6	N	20589884
MGI:4839553	F	MP:0008784	craniorachischisis	Med12<tm1.1Hsch>/Med12<+>,Tg(CMV-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6	N	20589884
MGI:4839553	F	MP:0004601	abnormal vertebral spinous process morphology	Med12<tm1.1Hsch>/Med12<+>,Tg(CMV-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6	N	20589884
MGI:4839553	F	MP:0004603	absent vertebral arch	Med12<tm1.1Hsch>/Med12<+>,Tg(CMV-cre)1Cgn/0	involves: 129S6/SvEvTac * C57BL/6	N	20589884
MGI:4839563	F	MP:0008000	increased ovary tumor incidence	Tg(Amhr2-SV40TAg)1Dcco/0	(C57BL/6 x C3H)F1	N	12649204
MGI:4839563	F	MP:0003579	increased ovarian carcinoma incidence	Tg(Amhr2-SV40TAg)1Dcco/0	(C57BL/6 x C3H)F1	N	12649204
MGI:4839563	F	MP:0003675	kidney cyst	Tg(Amhr2-SV40TAg)1Dcco/0	(C57BL/6 x C3H)F1	N	12649204
MGI:4839563	F	MP:0001926	female infertility	Tg(Amhr2-SV40TAg)1Dcco/0	(C57BL/6 x C3H)F1	N	12649204
MGI:4839563	M	MP:0006262	increased testis tumor incidence	Tg(Amhr2-SV40TAg)1Dcco/0	(C57BL/6 x C3H)F1	N	12649204
MGI:4839926	M	MP:0002073	abnormal hair growth	Eda<Ta-33H>/Y	Not Specified	N	MGI:52792
MGI:4839926	M	MP:0005371	limbs/digits/tail phenotype	Eda<Ta-33H>/Y	Not Specified	Y	MGI:52792
MGI:4839926	M	MP:0005382	craniofacial phenotype	Eda<Ta-33H>/Y	Not Specified	Y	MGI:52792
MGI:4839926	M	MP:0002832	coarse hair	Eda<Ta-33H>/Y	Not Specified	N	MGI:52792
MGI:4839926	M	MP:0002074	abnormal hair texture	Eda<Ta-33H>/Y	Not Specified	N	MGI:52792
MGI:4839929	F	MP:0010231	transverse fur striping	Eda<Ta-33H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4839929	F	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta-33H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840021	M	MP:0002073	abnormal hair growth	Eda<Ta-32H>/Y	Not Specified	N	MGI:52792
MGI:4840021	M	MP:0000585	kinked tail	Eda<Ta-32H>/Y	Not Specified	N	MGI:52792
MGI:4840021	M	MP:0000367	abnormal coat/ hair morphology	Eda<Ta-32H>/Y	Not Specified	N	MGI:52792
MGI:4840021	M	MP:0002074	abnormal hair texture	Eda<Ta-32H>/Y	Not Specified	N	MGI:52792
MGI:4840021	M	MP:0002111	abnormal tail morphology	Eda<Ta-32H>/Y	Not Specified	N	MGI:52792
MGI:4840021	M	MP:0000119	abnormal tooth eruption	Eda<Ta-32H>/Y	Not Specified	N	MGI:52792
MGI:4840021	M	MP:0006365	absent guard hair	Eda<Ta-32H>/Y	Not Specified	N	MGI:52792
MGI:4840021	M	MP:0009003	abnormal vibrissa number	Eda<Ta-32H>/Y	Not Specified	N	MGI:52792
MGI:4840021	M	MP:0006366	absent zigzag hairs	Eda<Ta-32H>/Y	Not Specified	N	MGI:52792
MGI:4840021	M	MP:0005287	narrow eye opening	Eda<Ta-32H>/Y	Not Specified	N	MGI:52792
MGI:4840021	M	MP:0010233	hairless tail	Eda<Ta-32H>/Y	Not Specified	N	MGI:52792
MGI:4840029	F	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta-32H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840029	F	MP:0010231	transverse fur striping	Eda<Ta-32H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840029	F	MP:0002074	abnormal hair texture	Eda<Ta-32H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840029	F	MP:0009659	striated fur	Eda<Ta-32H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840031	F	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta-30H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840031	F	MP:0002074	abnormal hair texture	Eda<Ta-30H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840031	F	MP:0010231	transverse fur striping	Eda<Ta-30H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840031	F	MP:0009659	striated fur	Eda<Ta-30H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840032	M	MP:0000585	kinked tail	Eda<Ta-30H>/Y	Not Specified	N	MGI:52792
MGI:4840032	M	MP:0010233	hairless tail	Eda<Ta-30H>/Y	Not Specified	N	MGI:52792
MGI:4840032	M	MP:0012078	abnormal tail ring morphology	Eda<Ta-30H>/Y	Not Specified	N	MGI:52792
MGI:4840032	M	MP:0005287	narrow eye opening	Eda<Ta-30H>/Y	Not Specified	N	MGI:52792
MGI:4840032	M	MP:0000367	abnormal coat/ hair morphology	Eda<Ta-30H>/Y	Not Specified	N	MGI:52792
MGI:4840032	M	MP:0006366	absent zigzag hairs	Eda<Ta-30H>/Y	Not Specified	N	MGI:52792
MGI:4840032	M	MP:0002073	abnormal hair growth	Eda<Ta-30H>/Y	Not Specified	N	MGI:52792
MGI:4840032	M	MP:0000119	abnormal tooth eruption	Eda<Ta-30H>/Y	Not Specified	N	MGI:52792
MGI:4840032	M	MP:0002074	abnormal hair texture	Eda<Ta-30H>/Y	Not Specified	N	MGI:52792
MGI:4840032	M	MP:0006365	absent guard hair	Eda<Ta-30H>/Y	Not Specified	N	MGI:52792
MGI:4840032	M	MP:0009003	abnormal vibrissa number	Eda<Ta-30H>/Y	Not Specified	N	MGI:52792
MGI:4840033	M	MP:0012078	abnormal tail ring morphology	Eda<Ta-29H>/Y	Not Specified	N	MGI:52792
MGI:4840033	M	MP:0002074	abnormal hair texture	Eda<Ta-29H>/Y	Not Specified	N	MGI:52792
MGI:4840033	M	MP:0009003	abnormal vibrissa number	Eda<Ta-29H>/Y	Not Specified	N	MGI:52792
MGI:4840033	M	MP:0000585	kinked tail	Eda<Ta-29H>/Y	Not Specified	N	MGI:52792
MGI:4840033	M	MP:0000367	abnormal coat/ hair morphology	Eda<Ta-29H>/Y	Not Specified	N	MGI:52792
MGI:4840033	M	MP:0000119	abnormal tooth eruption	Eda<Ta-29H>/Y	Not Specified	N	MGI:52792
MGI:4840033	M	MP:0005287	narrow eye opening	Eda<Ta-29H>/Y	Not Specified	N	MGI:52792
MGI:4840033	M	MP:0010233	hairless tail	Eda<Ta-29H>/Y	Not Specified	N	MGI:52792
MGI:4840033	M	MP:0006365	absent guard hair	Eda<Ta-29H>/Y	Not Specified	N	MGI:52792
MGI:4840033	M	MP:0002073	abnormal hair growth	Eda<Ta-29H>/Y	Not Specified	N	MGI:52792
MGI:4840033	M	MP:0006366	absent zigzag hairs	Eda<Ta-29H>/Y	Not Specified	N	MGI:52792
MGI:4840034	F	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta-29H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840034	F	MP:0009659	striated fur	Eda<Ta-29H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840034	F	MP:0010231	transverse fur striping	Eda<Ta-29H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840034	F	MP:0002074	abnormal hair texture	Eda<Ta-29H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840035	M	MP:0002074	abnormal hair texture	Eda<Ta-26H>/Y	Not Specified	N	MGI:52792
MGI:4840035	M	MP:0005382	craniofacial phenotype	Eda<Ta-26H>/Y	Not Specified	Y	MGI:52792
MGI:4840035	M	MP:0002073	abnormal hair growth	Eda<Ta-26H>/Y	Not Specified	N	MGI:52792
MGI:4840035	M	MP:0002832	coarse hair	Eda<Ta-26H>/Y	Not Specified	N	MGI:52792
MGI:4840035	M	MP:0005371	limbs/digits/tail phenotype	Eda<Ta-26H>/Y	Not Specified	Y	MGI:52792
MGI:4840036	F	MP:0010231	transverse fur striping	Eda<Ta-26H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840036	F	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta-26H>/Eda<+>	Not Specified	N	MGI:52792
MGI:4840038	F	MP:0002738	hyperresponsive to tactile stimuli	Hprt1<tm1(tetO-Runx1,-EGFP)Enk>/Hprt1<+>,Sox10<tm2(rtTA)Weg>/Sox10<+>	involves: 129P2/OlaHsd	N	20187849
MGI:4840038	F	MP:0009703	decreased birth body size	Hprt1<tm1(tetO-Runx1,-EGFP)Enk>/Hprt1<+>,Sox10<tm2(rtTA)Weg>/Sox10<+>	involves: 129P2/OlaHsd	N	20187849
MGI:4840038	F	MP:0002095	abnormal skin pigmentation	Hprt1<tm1(tetO-Runx1,-EGFP)Enk>/Hprt1<+>,Sox10<tm2(rtTA)Weg>/Sox10<+>	involves: 129P2/OlaHsd	N	20187849
MGI:4840038	F	MP:0000964	small dorsal root ganglion	Hprt1<tm1(tetO-Runx1,-EGFP)Enk>/Hprt1<+>,Sox10<tm2(rtTA)Weg>/Sox10<+>	involves: 129P2/OlaHsd	N	20187849
MGI:4840038	F	MP:0002731	megacolon	Hprt1<tm1(tetO-Runx1,-EGFP)Enk>/Hprt1<+>,Sox10<tm2(rtTA)Weg>/Sox10<+>	involves: 129P2/OlaHsd	N	20187849
MGI:4840038	F	MP:0011085	postnatal lethality, complete penetrance	Hprt1<tm1(tetO-Runx1,-EGFP)Enk>/Hprt1<+>,Sox10<tm2(rtTA)Weg>/Sox10<+>	involves: 129P2/OlaHsd	N	20187849
MGI:4840234	F	MP:0001728	failure of embryo implantation	Brk1<Gt(DC0002)Wtsi>/Brk1<Gt(DC0002)Wtsi>	involves: 129P2/OlaHsd	N	20861187
MGI:4840384	M	MP:0001147	small testis	Bco2<tm1Dnp>/Bco2<tm1Dnp>	involves: 129S6/SvEvTac * C57BL/6	N	20962153
MGI:4840384	M	MP:0004910	decreased seminal vesicle weight	Bco2<tm1Dnp>/Bco2<tm1Dnp>	involves: 129S6/SvEvTac * C57BL/6	N	20962153
MGI:4840384	M	MP:0004852	decreased testis weight	Bco2<tm1Dnp>/Bco2<tm1Dnp>	involves: 129S6/SvEvTac * C57BL/6	N	20962153
MGI:4840407	F	MP:0005070	impaired natural killer cell mediated cytotoxicity	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>,Sh2d1b1/Sh2d1b2<tm1.1Cpt>/Sh2d1b1/Sh2d1b2<tm1.1Cpt>	involves: 129S4/SvJae * BALB/cJ	N	20962259
MGI:4840408	F	MP:0005070	impaired natural killer cell mediated cytotoxicity	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>,Sh2d1b1/Sh2d1b2<tm1.1Cpt>/Sh2d1b1/Sh2d1b2<tm1.1Cpt>	involves: 129S4/SvJae * BALB/cJ	N	20962259
MGI:4840409	F	MP:0005070	impaired natural killer cell mediated cytotoxicity	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>	involves: 129S4/SvJae	N	20962259
MGI:4840463	M	MP:0001156	abnormal spermatogenesis	Rxfp2<m1Lja>/Rxfp2<m1Lja>	C57BL/6J-Rxfp2<m1Lja>	N	20963592
MGI:4840463	M	MP:0002286	cryptorchism	Rxfp2<m1Lja>/Rxfp2<m1Lja>	C57BL/6J-Rxfp2<m1Lja>	N	20963592
MGI:4840463	M	MP:0001147	small testis	Rxfp2<m1Lja>/Rxfp2<m1Lja>	C57BL/6J-Rxfp2<m1Lja>	N	20963592
MGI:4840463	M	MP:0004852	decreased testis weight	Rxfp2<m1Lja>/Rxfp2<m1Lja>	C57BL/6J-Rxfp2<m1Lja>	N	20963592
MGI:4840463	M	MP:0004901	decreased male germ cell number	Rxfp2<m1Lja>/Rxfp2<m1Lja>	C57BL/6J-Rxfp2<m1Lja>	N	20963592
MGI:4840514	F	MP:0005168	abnormal female meiosis	Rec8<tm1.1Kktk>/Rec8<tm1.1Kktk>	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	20971813
MGI:4840515	F	MP:0005168	abnormal female meiosis	Rad21<tm1.1Kktk>/Rad21<tm1.1Kktk>	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	20971813
MGI:4840515	M	MP:0001922	reduced male fertility	Rad21<tm1.1Kktk>/Rad21<tm1.1Kktk>	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	20971813
MGI:4843198	F	MP:0001119	abnormal female reproductive system morphology	Lepr<tm4Mgmj>/Lepr<tm4Mgmj>	B6.Cg-Lepr<tm4Mgmj>	N	20068132
MGI:4843198	F	MP:0009009	absent estrous cycle	Lepr<tm4Mgmj>/Lepr<tm4Mgmj>	B6.Cg-Lepr<tm4Mgmj>	N	20068132
MGI:4843198	F	MP:0009021	absent estrus	Lepr<tm4Mgmj>/Lepr<tm4Mgmj>	B6.Cg-Lepr<tm4Mgmj>	N	20068132
MGI:4843198	F	MP:0001926	female infertility	Lepr<tm4Mgmj>/Lepr<tm4Mgmj>	B6.Cg-Lepr<tm4Mgmj>	N	20068132
MGI:4843199	F	MP:0009021	absent estrus	Lepr<tm1Mgmj>/Lepr<tm1Mgmj>	involves: 129	N	20068132
MGI:4843199	F	MP:0001926	female infertility	Lepr<tm1Mgmj>/Lepr<tm1Mgmj>	involves: 129	N	20068132
MGI:4843199	F	MP:0009009	absent estrous cycle	Lepr<tm1Mgmj>/Lepr<tm1Mgmj>	involves: 129	N	20068132
MGI:4843329	F	MP:0012431	increased lymphoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843329	F	MP:0002947	increased hemangioma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843329	F	MP:0001732	postnatal growth retardation	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843329	F	MP:0011090	perinatal lethality, incomplete penetrance	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843329	F	MP:0003667	increased hemangiosarcoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843329	F	MP:0006283	increased medulloblastoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843329	F	MP:0011086	postnatal lethality, incomplete penetrance	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843329	F	MP:0002083	premature death	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843329	F	MP:0002020	increased tumor incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843329	F	MP:0002027	increased lung adenocarcinoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843329	F	MP:0002048	increased lung adenoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843329	F	MP:0009703	decreased birth body size	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843329	F	MP:0009704	increased skin squamous cell carcinoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843329	F	MP:0002036	increased rhabdomyosarcoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Hprt1<+>	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0002036	increased rhabdomyosarcoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0002048	increased lung adenoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0002027	increased lung adenocarcinoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0012431	increased lymphoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0011086	postnatal lethality, incomplete penetrance	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0002083	premature death	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0001732	postnatal growth retardation	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0003667	increased hemangiosarcoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0002947	increased hemangioma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0009704	increased skin squamous cell carcinoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0009703	decreased birth body size	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0002020	increased tumor incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0006283	increased medulloblastoma incidence	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843330	M	MP:0011090	perinatal lethality, incomplete penetrance	Gt(ROSA)26Sor<tm1(sb11)Njen>/Gt(ROSA)26Sor<+>,Hprt1<tm1(sb-Onco-Array)Peli>/Y	involves: 129S7/SvEvBrd	N	19064922
MGI:4843916	M	MP:0004958	enlarged prostate gland	Pten<tm1Hwu>/Pten<+>,Tg(ARR2/Pbsn-FGF8)3Prb/0,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	16489020
MGI:4843916	M	MP:0001167	prostate gland epithelial hyperplasia	Pten<tm1Hwu>/Pten<+>,Tg(ARR2/Pbsn-FGF8)3Prb/0,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	16489020
MGI:4843916	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Hwu>/Pten<+>,Tg(ARR2/Pbsn-FGF8)3Prb/0,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	16489020
MGI:4843916	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Hwu>/Pten<+>,Tg(ARR2/Pbsn-FGF8)3Prb/0,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	16489020
MGI:4844083	M	MP:0005305	prostate gland anterior lobe hyperplasia	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Fabp1-cre)1Jig/0	involves: 129S4/SvJae * FVB/N	N	16488991
MGI:4844083	M	MP:0001756	abnormal urination	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Fabp1-cre)1Jig/0	involves: 129S4/SvJae * FVB/N	N	16488991
MGI:4844083	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Fabp1-cre)1Jig/0	involves: 129S4/SvJae * FVB/N	N	16488991
MGI:4844310	F	MP:0020330	increased capillary density	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>,Flt1<tm1Jrt>/Flt1<+>	involves: C3HA * C57BL/6Ros	N	20705734
MGI:4844310	F	MP:0000730	increased satellite cell number	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>,Flt1<tm1Jrt>/Flt1<+>	involves: C3HA * C57BL/6Ros	N	20705734
MGI:4844310	F	MP:0000733	abnormal muscle development	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>,Flt1<tm1Jrt>/Flt1<+>	involves: C3HA * C57BL/6Ros	N	20705734
MGI:4844310	F	MP:0005369	muscle phenotype	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>,Flt1<tm1Jrt>/Flt1<+>	involves: C3HA * C57BL/6Ros	Y	20705734
MGI:4844310	F	MP:0002128	abnormal blood circulation	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>,Flt1<tm1Jrt>/Flt1<+>	involves: C3HA * C57BL/6Ros	N	20705734
MGI:4844310	F	MP:0009398	abnormal skeletal muscle fiber size	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>,Flt1<tm1Jrt>/Flt1<+>	involves: C3HA * C57BL/6Ros	N	20705734
MGI:4844310	F	MP:0005620	abnormal muscle contractility	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>,Flt1<tm1Jrt>/Flt1<+>	involves: C3HA * C57BL/6Ros	N	20705734
MGI:4844310	F	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>,Flt1<tm1Jrt>/Flt1<+>	involves: C3HA * C57BL/6Ros	N	20705734
MGI:4844311	F	MP:0001260	increased body weight	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>,Flt1<tm1Jrt>/Flt1<+>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C3HA * C57BL/6Ros	N	20705734
MGI:4844311	F	MP:0001661	extended life span	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>,Flt1<tm1Jrt>/Flt1<+>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C3HA * C57BL/6Ros	N	20705734
MGI:4844311	F	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx-5Cv>/Dmd<mdx-5Cv>,Flt1<tm1Jrt>/Flt1<+>,Utrn<tm1Jrs>/Utrn<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C3HA * C57BL/6Ros	N	20705734
MGI:4847555	F	MP:0006270	abnormal mammary gland growth during lactation	Stat5a<tm2Mam>/Stat5a<tm2Mam>,Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(MMTV-cre)1Mam/0	involves: 129S6/SvEvTac * FVB/N	N	19833766
MGI:4847555	F	MP:0009506	abnormal mammary gland alveolus morphology	Stat5a<tm2Mam>/Stat5a<tm2Mam>,Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(MMTV-cre)1Mam/0	involves: 129S6/SvEvTac * FVB/N	N	19833766
MGI:4847555	F	MP:0010249	lactation failure	Stat5a<tm2Mam>/Stat5a<tm2Mam>,Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(MMTV-cre)1Mam/0	involves: 129S6/SvEvTac * FVB/N	N	19833766
MGI:4847556	F	MP:0009506	abnormal mammary gland alveolus morphology	Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(MMTV-cre)1Mam/0	involves: 129S6/SvEvTac * FVB/N	N	19833766
MGI:4847556	F	MP:0006270	abnormal mammary gland growth during lactation	Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(MMTV-cre)1Mam/0	involves: 129S6/SvEvTac * FVB/N	N	19833766
MGI:4847556	F	MP:0010249	lactation failure	Stat5b<tm1Mam>/Stat5b<tm1Mam>,Tg(MMTV-cre)1Mam/0	involves: 129S6/SvEvTac * FVB/N	N	19833766
MGI:4847568	M	MP:0000585	kinked tail	Eda<Ta-23H>/Y	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847568	M	MP:0002073	abnormal hair growth	Eda<Ta-23H>/Y	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847568	M	MP:0010233	hairless tail	Eda<Ta-23H>/Y	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847568	M	MP:0000367	abnormal coat/ hair morphology	Eda<Ta-23H>/Y	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847568	M	MP:0012078	abnormal tail ring morphology	Eda<Ta-23H>/Y	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847569	F	MP:0009659	striated fur	Eda<Ta-23H>/Eda<+>	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847569	F	MP:0010231	transverse fur striping	Eda<Ta-23H>/Eda<+>	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847569	F	MP:0002075	abnormal coat/hair pigmentation	Eda<Ta-23H>/Eda<+>	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847569	F	MP:0006366	absent zigzag hairs	Eda<Ta-23H>/Eda<+>	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847569	F	MP:0000372	irregular coat pigmentation	Eda<Ta-23H>/Eda<+>	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847570	F	MP:0002073	abnormal hair growth	Eda<Ta-23H>/Eda<Ta-23H>	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847570	F	MP:0000367	abnormal coat/ hair morphology	Eda<Ta-23H>/Eda<Ta-23H>	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847570	F	MP:0000585	kinked tail	Eda<Ta-23H>/Eda<Ta-23H>	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847570	F	MP:0012078	abnormal tail ring morphology	Eda<Ta-23H>/Eda<Ta-23H>	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847570	F	MP:0010233	hairless tail	Eda<Ta-23H>/Eda<Ta-23H>	C3H101H-Eda<Ta-23H>/H	N	MGI:4840039
MGI:4847573	F	MP:0008706	decreased interleukin-6 secretion	Pim2<tm1.1Lex>/Pim2<tm1.1Lex>	involves: 129S/SvEvBrd * C57BL/6	N	20465571
MGI:4847591	F	MP:0004832	enlarged ovary	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae	N	18606860
MGI:4847591	F	MP:0031424	enhanced female fertility	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae	N	18606860
MGI:4847591	F	MP:0031423	abnormal luteolysis	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae	N	18606860
MGI:4847591	F	MP:0001131	abnormal ovarian follicle morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae	N	18606860
MGI:4847591	F	MP:0031016	decreased granulosa cell apoptosis	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae	N	18606860
MGI:4847591	F	MP:0002006	neoplasm	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae	Y	18606860
MGI:4847591	F	MP:0001133	impaired luteal cell differentiation	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae	N	18606860
MGI:4847591	F	MP:0031019	increased granulosa cell proliferation	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae	N	18606860
MGI:4847591	F	MP:0031421	increased superovulation rate	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae	N	18606860
MGI:4847591	F	MP:0002681	increased corpora lutea number	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae	N	18606860
MGI:4847601	M	MP:0000659	prostate gland hyperplasia	Gt(ROSA)26Sor<tm1(cre/ERT)Nat>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129 * 129S4/SvJae * BALB/c * C57BL/6	N	18043744
MGI:4847601	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Gt(ROSA)26Sor<tm1(cre/ERT)Nat>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129 * 129S4/SvJae * BALB/c * C57BL/6	N	18043744
MGI:4847601	M	MP:0010279	increased gastrointestinal tumor incidence	Gt(ROSA)26Sor<tm1(cre/ERT)Nat>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129 * 129S4/SvJae * BALB/c * C57BL/6	N	18043744
MGI:4847601	M	MP:0010357	increased prostate gland tumor incidence	Gt(ROSA)26Sor<tm1(cre/ERT)Nat>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129 * 129S4/SvJae * BALB/c * C57BL/6	N	18043744
MGI:4847601	F	MP:0009092	endometrium hyperplasia	Gt(ROSA)26Sor<tm1(cre/ERT)Nat>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129 * 129S4/SvJae * BALB/c * C57BL/6	N	18043744
MGI:4847608	F	MP:0000208	decreased hematocrit	F9<tm3Dws>/F9<tm3Dws>	B6.129P2-F9<tm3Dws>	N	19583826
MGI:4847608	F	MP:0005606	increased bleeding time	F9<tm3Dws>/F9<tm3Dws>	B6.129P2-F9<tm3Dws>	N	19583826
MGI:4847609	F	MP:0005606	increased bleeding time	F9<tm1Dws>/F9<tm1Dws>	involves: 129P2/OlaHsd	N	19583826
MGI:4847609	F	MP:0000208	decreased hematocrit	F9<tm1Dws>/F9<tm1Dws>	involves: 129P2/OlaHsd	N	19583826
MGI:4847609	F	MP:0002551	abnormal blood coagulation	F9<tm1Dws>/F9<tm1Dws>	involves: 129P2/OlaHsd	N	19583826
MGI:4847609	F	MP:0009763	increased susceptibility to induced morbidity/mortality	F9<tm1Dws>/F9<tm1Dws>	involves: 129P2/OlaHsd	N	19583826
MGI:4847610	M	MP:0005606	increased bleeding time	F9<tm1Dws>/Y	involves: 129P2/OlaHsd	N	19583826
MGI:4847610	M	MP:0009763	increased susceptibility to induced morbidity/mortality	F9<tm1Dws>/Y	involves: 129P2/OlaHsd	N	19583826
MGI:4847610	M	MP:0002551	abnormal blood coagulation	F9<tm1Dws>/Y	involves: 129P2/OlaHsd	N	19583826
MGI:4847610	M	MP:0000208	decreased hematocrit	F9<tm1Dws>/Y	involves: 129P2/OlaHsd	N	19583826
MGI:4847611	M	MP:0005606	increased bleeding time	F9<tm3Dws>/Y	B6.129P2-F9<tm3Dws>	N	19583826
MGI:4847611	M	MP:0000208	decreased hematocrit	F9<tm3Dws>/Y	B6.129P2-F9<tm3Dws>	N	19583826
MGI:4847611	M	MP:0002551	abnormal blood coagulation	F9<tm3Dws>/Y	B6.129P2-F9<tm3Dws>	N	19583826
MGI:4847617	M	MP:0004962	decreased prostate gland weight	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CAG-fat-1)1Jxk/0,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	N	17607361
MGI:4847667	F	MP:0000217	abnormal leukocyte cell number	Gata1<tm6Sho>/Gata1<tm6Sho>	involves: 129S1/Sv * BALB/c	N	17060636
MGI:4847667	F	MP:0008609	decreased circulating interleukin-13 level	Gata1<tm6Sho>/Gata1<tm6Sho>	involves: 129S1/Sv * BALB/c	N	17060636
MGI:4847667	F	MP:0005012	decreased eosinophil cell number	Gata1<tm6Sho>/Gata1<tm6Sho>	involves: 129S1/Sv * BALB/c	N	17060636
MGI:4847667	F	MP:0008603	decreased circulating interleukin-4 level	Gata1<tm6Sho>/Gata1<tm6Sho>	involves: 129S1/Sv * BALB/c	N	17060636
MGI:4847667	F	MP:0002133	abnormal respiratory system physiology	Gata1<tm6Sho>/Gata1<tm6Sho>	involves: 129S1/Sv * BALB/c	N	15375268
MGI:4847667	F	MP:0005016	decreased lymphocyte cell number	Gata1<tm6Sho>/Gata1<tm6Sho>	involves: 129S1/Sv * BALB/c	N	17060636
MGI:4847667	F	MP:0000219	increased neutrophil cell number	Gata1<tm6Sho>/Gata1<tm6Sho>	involves: 129S1/Sv * BALB/c	N	17060636
MGI:4847667	F	MP:0005388	respiratory system phenotype	Gata1<tm6Sho>/Gata1<tm6Sho>	involves: 129S1/Sv * BALB/c	Y	15375268
MGI:4847667	F	MP:0009676	abnormal hemostasis	Gata1<tm6Sho>/Gata1<tm6Sho>	involves: 129S1/Sv * BALB/c	N	17060636
MGI:4847667	F	MP:0002267	abnormal bronchiole morphology	Gata1<tm6Sho>/Gata1<tm6Sho>	involves: 129S1/Sv * BALB/c	N	15375268
MGI:4848122	M	MP:0005565	increased blood urea nitrogen level	Rnl23/?	C57BL/6J-Rnl23	N	MGI:2656149
MGI:4848125	M	MP:0005565	increased blood urea nitrogen level	Rnl32/?	C57BL/6J-Rnl32	N	MGI:2656149
MGI:4848133	M	MP:0000659	prostate gland hyperplasia	Pten<tm1Rps>/Pten<+>,Rictor<Gt(RRR347)Byg>/Rictor<+>	involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6	N	19185849
MGI:4848147	M	MP:0009734	abnormal prostate gland duct morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Rictor<tm1.1Mgn>/Rictor<tm1.1Mgn>	involves: 129S4/SvJae * 129S6/SvEvTac	N	19185849
MGI:4848147	M	MP:0001168	abnormal prostate gland epithelium morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Rictor<tm1.1Mgn>/Rictor<tm1.1Mgn>	involves: 129S4/SvJae * 129S6/SvEvTac	N	19185849
MGI:4848150	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae	N	19185849
MGI:4848150	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae	N	19185849
MGI:4849446	F	MP:0005389	reproductive system phenotype	Col1a1<tm1(tetO-Lin28a)Gqda>/Col1a1<+>	involves: 129S4/SvJae * C57BL/6 * CD-1	Y	20512147
MGI:4849446	F	MP:0002636	delayed vaginal opening	Col1a1<tm1(tetO-Lin28a)Gqda>/Col1a1<+>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	20512147
MGI:4849446	F	MP:0001934	increased litter size	Col1a1<tm1(tetO-Lin28a)Gqda>/Col1a1<+>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	20512147
MGI:4849446	F	MP:0001938	delayed sexual maturation	Col1a1<tm1(tetO-Lin28a)Gqda>/Col1a1<+>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	20512147
MGI:4849446	F	MP:0008976	delayed female fertility	Col1a1<tm1(tetO-Lin28a)Gqda>/Col1a1<+>	involves: 129S4/SvJae * C57BL/6 * CD-1	N	20512147
MGI:4849535	M	MP:0000534	abnormal ureter morphology	Hprt1<tm1(CAG-Sox9,-EGFP)Akis>/Y,Tbx18<tm4(cre)Akis>/Tbx18<+>	involves: 129/Sv * 129S1/SvImJ * NMRI	N	20881014
MGI:4849535	M	MP:0011426	abnormal ureter smooth muscle morphology	Hprt1<tm1(CAG-Sox9,-EGFP)Akis>/Y,Tbx18<tm4(cre)Akis>/Tbx18<+>	involves: 129/Sv * 129S1/SvImJ * NMRI	N	20881014
MGI:4849545	M	MP:0003871	abnormal myelin sheath morphology	Plp1<jp-rsh>/Y	C3H * C57BL/6 * STOCK Rb(1.3)1Bnr	N	8522972
MGI:4849545	M	MP:0000921	demyelination	Plp1<jp-rsh>/Y	C3H * C57BL/6 * STOCK Rb(1.3)1Bnr	N	8522972
MGI:4849548	F	MP:0004777	abnormal phospholipid level	Plp1<jp-rsh>/Plp1<jp-rsh>	C3H * C57BL/6 * STOCK Rb(1.3)1Bnr	N	8522972
MGI:4849548	F	MP:0003871	abnormal myelin sheath morphology	Plp1<jp-rsh>/Plp1<jp-rsh>	C3H * C57BL/6 * STOCK Rb(1.3)1Bnr	N	8522972
MGI:4849927	M	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-8J>/Y	involves: C3HeB/FeJ * C57BL/6J	N	MGI:64397
MGI:4849927	M	MP:0000755	hindlimb paralysis	Atp7a<Mo-8J>/Y	involves: C3HeB/FeJ * C57BL/6J	N	MGI:64397
MGI:4849927	M	MP:0002082	postnatal lethality	Atp7a<Mo-8J>/Y	involves: C3HeB/FeJ * C57BL/6J	N	9147645
MGI:4849927	M	MP:0001279	wavy vibrissae	Atp7a<Mo-8J>/Y	involves: C3HeB/FeJ * C57BL/6J	N	MGI:64397
MGI:4849927	M	MP:0000371	diluted coat color	Atp7a<Mo-8J>/Y	involves: C3HeB/FeJ * C57BL/6J	N	MGI:64397
MGI:4849928	F	MP:0001279	wavy vibrissae	Atp7a<Mo-8J>/Atp7a<+>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:64397
MGI:4849928	F	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-8J>/Atp7a<+>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:64397
MGI:4849928	F	MP:0000755	hindlimb paralysis	Atp7a<Mo-8J>/Atp7a<+>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:64397
MGI:4849928	F	MP:0010389	mosaic coat color	Atp7a<Mo-8J>/Atp7a<+>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:64397
MGI:4849928	F	MP:0000371	diluted coat color	Atp7a<Mo-8J>/Atp7a<+>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:64397
MGI:4849928	F	MP:0000372	irregular coat pigmentation	Atp7a<Mo-8J>/Atp7a<+>	involves: C3HeB/FeJ * C57BL/6J	N	MGI:64397
MGI:4867174	M	MP:0014052	increased male germ cell apoptosis	Del(11Cxcl16-Zmynd15)1Ifc/Del(11Cxcl16-Zmynd15)1Ifc	involves: 129S4/SvJae * C57BL/6	N	20675388
MGI:4867174	M	MP:0001156	abnormal spermatogenesis	Del(11Cxcl16-Zmynd15)1Ifc/Del(11Cxcl16-Zmynd15)1Ifc	involves: 129S4/SvJae * C57BL/6	N	20675388
MGI:4867174	M	MP:0005159	azoospermia	Del(11Cxcl16-Zmynd15)1Ifc/Del(11Cxcl16-Zmynd15)1Ifc	involves: 129S4/SvJae * C57BL/6	N	20675388
MGI:4867174	M	MP:0004850	abnormal testis weight	Del(11Cxcl16-Zmynd15)1Ifc/Del(11Cxcl16-Zmynd15)1Ifc	involves: 129S4/SvJae * C57BL/6	N	20675388
MGI:4867174	M	MP:0001925	male infertility	Del(11Cxcl16-Zmynd15)1Ifc/Del(11Cxcl16-Zmynd15)1Ifc	involves: 129S4/SvJae * C57BL/6	N	20675388
MGI:4867234	M	MP:0001925	male infertility	Smc1b<tm1Jess>/Smc1b<tm2.2Jess>	involves: 129S6/SvEvTac * C57BL/6 * SJL	N	20817531
MGI:4867234	F	MP:0001926	female infertility	Smc1b<tm1Jess>/Smc1b<tm2.2Jess>	involves: 129S6/SvEvTac * C57BL/6 * SJL	N	20817531
MGI:4867234	M	MP:0001155	arrest of spermatogenesis	Smc1b<tm1Jess>/Smc1b<tm2.2Jess>	involves: 129S6/SvEvTac * C57BL/6 * SJL	N	20817531
MGI:4867234	M	MP:0005159	azoospermia	Smc1b<tm1Jess>/Smc1b<tm2.2Jess>	involves: 129S6/SvEvTac * C57BL/6 * SJL	N	20817531
MGI:4867396	M	MP:0006380	abnormal spermatid morphology	Tmf1<tm1Unir>/Tmf1<tm1Unir>	involves: 129/Sv * ICR	N	20691678
MGI:4867396	M	MP:0001925	male infertility	Tmf1<tm1Unir>/Tmf1<tm1Unir>	involves: 129/Sv * ICR	N	20691678
MGI:4867396	M	MP:0008839	absent acrosome	Tmf1<tm1Unir>/Tmf1<tm1Unir>	involves: 129/Sv * ICR	N	20691678
MGI:4867396	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Tmf1<tm1Unir>/Tmf1<tm1Unir>	involves: 129/Sv * ICR	N	20691678
MGI:4867396	M	MP:0004852	decreased testis weight	Tmf1<tm1Unir>/Tmf1<tm1Unir>	involves: 129/Sv * ICR	N	20691678
MGI:4867396	M	MP:0009831	abnormal sperm midpiece morphology	Tmf1<tm1Unir>/Tmf1<tm1Unir>	involves: 129/Sv * ICR	N	20691678
MGI:4867396	M	MP:0002675	asthenozoospermia	Tmf1<tm1Unir>/Tmf1<tm1Unir>	involves: 129/Sv * ICR	N	20691678
MGI:4867396	M	MP:0002686	globozoospermia	Tmf1<tm1Unir>/Tmf1<tm1Unir>	involves: 129/Sv * ICR	N	20691678
MGI:4867469	M	MP:0009230	abnormal sperm head morphology	Fabp9<tm1Vise>/Fabp9<tm1Vise>	involves: 129S6/SvEvTac * C57BL/6	N	20920498
MGI:4867472	M	MP:0001925	male infertility	Sirt6<tm2.1Cxd>/Sirt6<tm2.1Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	N	20847051
MGI:4867472	F	MP:0001923	reduced female fertility	Sirt6<tm2.1Cxd>/Sirt6<tm2.1Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	N	20847051
MGI:4867472	F	MP:0001382	abnormal nursing	Sirt6<tm2.1Cxd>/Sirt6<tm2.1Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	N	20847051
MGI:4867473	M	MP:0001925	male infertility	Sirt6<tm2.2Cxd>/Sirt6<tm2.2Cxd>	involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	N	20847051
MGI:4867473	F	MP:0001382	abnormal nursing	Sirt6<tm2.2Cxd>/Sirt6<tm2.2Cxd>	involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	N	20847051
MGI:4867473	F	MP:0001923	reduced female fertility	Sirt6<tm2.2Cxd>/Sirt6<tm2.2Cxd>	involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	N	20847051
MGI:4867484	F	MP:0001926	female infertility	Gjb2<tm2.2Kwi>/Gjb2<+>,Tg(Pgk1-cre)1Lni/0	involves: 129/Sv * 129P2/OlaHsd * BALB/c * C57BL/6	N	20926451
MGI:4867489	F	MP:0001923	reduced female fertility	Kmt2b<tm2.1Afst>/Kmt2b<tm2.1Afst>	involves: 129 * C57BL/6	N	20808952
MGI:4867490	F	MP:0001923	reduced female fertility	Kmt2b<tm2.1Afst>/Kmt2b<+>	involves: 129 * C57BL/6	N	20808952
MGI:4867492	F	MP:0031239	increased atretic ovarian follicle number	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	20808952
MGI:4867492	F	MP:0031381	decreased secondary ovarian follicle number	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	20808952
MGI:4867492	F	MP:0011121	decreased primordial ovarian follicle number	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	20808952
MGI:4867492	F	MP:0008871	abnormal ovarian follicle number	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	20808952
MGI:4867492	F	MP:0011125	decreased primary ovarian follicle number	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	20808952
MGI:4867492	F	MP:0001923	reduced female fertility	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	20808952
MGI:4867493	F	MP:0011124	increased primary ovarian follicle number	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Gdf9-icre)5092Coo/0	involves: 129 * 129P2/OlaHsd * C57BL/6	N	20808952
MGI:4867493	F	MP:0001926	female infertility	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Gdf9-icre)5092Coo/0	involves: 129 * 129P2/OlaHsd * C57BL/6	N	20808952
MGI:4867493	F	MP:0031239	increased atretic ovarian follicle number	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Gdf9-icre)5092Coo/0	involves: 129 * 129P2/OlaHsd * C57BL/6	N	20808952
MGI:4867493	F	MP:0011121	decreased primordial ovarian follicle number	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Gdf9-icre)5092Coo/0	involves: 129 * 129P2/OlaHsd * C57BL/6	N	20808952
MGI:4867493	F	MP:0010767	abnormal female meiosis I arrest	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Gdf9-icre)5092Coo/0	involves: 129 * 129P2/OlaHsd * C57BL/6	N	20808952
MGI:4867493	F	MP:0008871	abnormal ovarian follicle number	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Gdf9-icre)5092Coo/0	involves: 129 * 129P2/OlaHsd * C57BL/6	N	20808952
MGI:4867493	F	MP:0031383	increased secondary ovarian follicle number	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Gdf9-icre)5092Coo/0	involves: 129 * 129P2/OlaHsd * C57BL/6	N	20808952
MGI:4867493	F	MP:0002678	increased follicle recruitment	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Gdf9-icre)5092Coo/0	involves: 129 * 129P2/OlaHsd * C57BL/6	N	20808952
MGI:4867493	F	MP:0031420	decreased superovulation rate	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Gdf9-icre)5092Coo/0	involves: 129 * 129P2/OlaHsd * C57BL/6	N	20808952
MGI:4867494	F	MP:0011121	decreased primordial ovarian follicle number	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Zp3-cre)3Mrt/0	involves: 129 * 129P2/OlaHsd * C57BL/6 * FVB/N	N	20808952
MGI:4867494	F	MP:0031239	increased atretic ovarian follicle number	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Zp3-cre)3Mrt/0	involves: 129 * 129P2/OlaHsd * C57BL/6 * FVB/N	N	20808952
MGI:4867494	F	MP:0008871	abnormal ovarian follicle number	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Zp3-cre)3Mrt/0	involves: 129 * 129P2/OlaHsd * C57BL/6 * FVB/N	N	20808952
MGI:4867494	F	MP:0031420	decreased superovulation rate	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Zp3-cre)3Mrt/0	involves: 129 * 129P2/OlaHsd * C57BL/6 * FVB/N	N	20808952
MGI:4867494	F	MP:0001926	female infertility	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Tg(Zp3-cre)3Mrt/0	involves: 129 * 129P2/OlaHsd * C57BL/6 * FVB/N	N	20808952
MGI:4867495	F	MP:0001926	female infertility	Kmt2b<tm1Afst>/Kmt2b<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	N	20808952
MGI:4867503	M	MP:0001516	abnormal motor coordination/balance	Nlgn3<tm1.1Htz>/Y	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867503	M	MP:0002862	abnormal righting response	Nlgn3<tm1.1Htz>/Y	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867503	M	MP:0002865	increased growth rate	Nlgn3<tm1.1Htz>/Y	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867503	M	MP:0002757	decreased vertical activity	Nlgn3<tm1.1Htz>/Y	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867503	M	MP:0020351	decreased vocalization	Nlgn3<tm1.1Htz>/Y	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867503	M	MP:0003631	nervous system phenotype	Nlgn3<tm1.1Htz>/Y	involves: C57BL/6 * FVB/N	Y	19360662
MGI:4867503	M	MP:0002797	increased thigmotaxis	Nlgn3<tm1.1Htz>/Y	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867503	M	MP:0001489	decreased startle reflex	Nlgn3<tm1.1Htz>/Y	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867503	M	MP:0003858	enhanced coordination	Nlgn3<tm1.1Htz>/Y	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867503	M	MP:0001463	abnormal spatial learning	Nlgn3<tm1.1Htz>/Y	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867503	M	MP:0001405	impaired coordination	Nlgn3<tm1.1Htz>/Y	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867504	F	MP:0001463	abnormal spatial learning	Nlgn3<tm1.1Htz>/Nlgn3<tm1.1Htz>	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867504	F	MP:0002797	increased thigmotaxis	Nlgn3<tm1.1Htz>/Nlgn3<tm1.1Htz>	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867504	F	MP:0002862	abnormal righting response	Nlgn3<tm1.1Htz>/Nlgn3<tm1.1Htz>	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867504	F	MP:0001732	postnatal growth retardation	Nlgn3<tm1.1Htz>/Nlgn3<tm1.1Htz>	involves: C57BL/6 * FVB/N	N	19360662
MGI:4867504	F	MP:0002063	abnormal learning/memory/conditioning	Nlgn3<tm1.1Htz>/Nlgn3<tm1.1Htz>	involves: C57BL/6 * FVB/N	N	19360662
MGI:4868202	M	MP:0009325	necrospermia	Pfdn5<nmf5a>/Pfdn5<nmf5a>	C57BL/6-Pfdn5<nmf5a>	N	20956523
MGI:4868202	M	MP:0001925	male infertility	Pfdn5<nmf5a>/Pfdn5<nmf5a>	C57BL/6-Pfdn5<nmf5a>	N	20956523
MGI:4868202	M	MP:0002687	oligozoospermia	Pfdn5<nmf5a>/Pfdn5<nmf5a>	C57BL/6-Pfdn5<nmf5a>	N	20956523
MGI:4868202	M	MP:0001147	small testis	Pfdn5<nmf5a>/Pfdn5<nmf5a>	C57BL/6-Pfdn5<nmf5a>	N	20956523
MGI:4868226	M	MP:0002216	abnormal seminiferous tubule morphology	Alkbh1<tm1Klng>/Alkbh1<tm1Klng>	involves: 129X1/SvJ * C57BL/6	N	21072209
MGI:4868226	M	MP:0005621	abnormal cell physiology	Alkbh1<tm1Klng>/Alkbh1<tm1Klng>	involves: 129X1/SvJ * C57BL/6	N	22965116
MGI:4868226	M	MP:0004901	decreased male germ cell number	Alkbh1<tm1Klng>/Alkbh1<tm1Klng>	involves: 129X1/SvJ * C57BL/6	N	21072209
MGI:4868226	M	MP:0001147	small testis	Alkbh1<tm1Klng>/Alkbh1<tm1Klng>	involves: 129X1/SvJ * C57BL/6	N	21072209
MGI:4868226	M	MP:0004852	decreased testis weight	Alkbh1<tm1Klng>/Alkbh1<tm1Klng>	involves: 129X1/SvJ * C57BL/6	N	21072209
MGI:4868226	M	MP:0001154	seminiferous tubule degeneration	Alkbh1<tm1Klng>/Alkbh1<tm1Klng>	involves: 129X1/SvJ * C57BL/6	N	21072209
MGI:4868231	M	MP:0005244	hemopericardium	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0003814	vascular smooth muscle hypoplasia	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0001634	internal hemorrhage	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0001784	abnormal fluid regulation	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0005312	pericardial effusion	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0011101	prenatal lethality, incomplete penetrance	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0001182	lung hemorrhage	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0001786	skin edema	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0001698	decreased embryo size	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0001672	abnormal embryo development	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0001914	hemorrhage	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0003052	omphalocele	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0004200	decreased fetal size	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0011110	preweaning lethality, incomplete penetrance	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0014273	abnormal skin vasculature morphology	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0000087	absent mandible	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0003719	abnormal pericyte morphology	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868231	M	MP:0004038	lymphangiectasis	Lpar4<tm1Sati>/Y	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0005244	hemopericardium	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0011110	preweaning lethality, incomplete penetrance	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0003719	abnormal pericyte morphology	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0000087	absent mandible	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0001784	abnormal fluid regulation	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0011101	prenatal lethality, incomplete penetrance	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0001914	hemorrhage	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0004038	lymphangiectasis	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0005312	pericardial effusion	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0001786	skin edema	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0004200	decreased fetal size	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0014273	abnormal skin vasculature morphology	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0001634	internal hemorrhage	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0003052	omphalocele	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0001672	abnormal embryo development	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0001182	lung hemorrhage	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0003814	vascular smooth muscle hypoplasia	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868233	F	MP:0001698	decreased embryo size	Lpar4<tm1Sati>/Lpar4<tm1Sati>	involves: C57BL/6	N	20713964
MGI:4868239	F	MP:0005431	decreased oocyte number	Adrm1<Gt(OST128063)Lex>/Adrm1<Gt(OST128063)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21048919
MGI:4868239	F	MP:0001926	female infertility	Adrm1<Gt(OST128063)Lex>/Adrm1<Gt(OST128063)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21048919
MGI:4868239	M	MP:0001925	male infertility	Adrm1<Gt(OST128063)Lex>/Adrm1<Gt(OST128063)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21048919
MGI:4868239	F	MP:0011122	absent primordial ovarian follicles	Adrm1<Gt(OST128063)Lex>/Adrm1<Gt(OST128063)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21048919
MGI:4868239	M	MP:0001153	small seminiferous tubules	Adrm1<Gt(OST128063)Lex>/Adrm1<Gt(OST128063)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21048919
MGI:4868239	M	MP:0008280	abnormal male germ cell apoptosis	Adrm1<Gt(OST128063)Lex>/Adrm1<Gt(OST128063)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21048919
MGI:4868239	F	MP:0001134	absent corpus luteum	Adrm1<Gt(OST128063)Lex>/Adrm1<Gt(OST128063)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21048919
MGI:4868239	M	MP:0005159	azoospermia	Adrm1<Gt(OST128063)Lex>/Adrm1<Gt(OST128063)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21048919
MGI:4868239	F	MP:0009444	ovarian follicular cyst	Adrm1<Gt(OST128063)Lex>/Adrm1<Gt(OST128063)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21048919
MGI:4868239	F	MP:0001125	abnormal oocyte morphology	Adrm1<Gt(OST128063)Lex>/Adrm1<Gt(OST128063)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21048919
MGI:4868239	F	MP:0001126	abnormal ovary morphology	Adrm1<Gt(OST128063)Lex>/Adrm1<Gt(OST128063)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21048919
MGI:4868239	F	MP:0001131	abnormal ovarian follicle morphology	Adrm1<Gt(OST128063)Lex>/Adrm1<Gt(OST128063)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21048919
MGI:4868377	F	MP:0013716	hypolactation	Mirc19<tm1.1Kcho>/Mirc19<tm1.1Kcho>	B6.129-Mirc19<tm1.1Kcho>	N	21057503
MGI:4868377	F	MP:0005376	homeostasis/metabolism phenotype	Mirc19<tm1.1Kcho>/Mirc19<tm1.1Kcho>	B6.129-Mirc19<tm1.1Kcho>	Y	21057503
MGI:4868377	F	MP:0003718	maternal effect	Mirc19<tm1.1Kcho>/Mirc19<tm1.1Kcho>	B6.129-Mirc19<tm1.1Kcho>	N	21057503
MGI:4868377	F	MP:0014057	abnormal mammary gland stroma morphology	Mirc19<tm1.1Kcho>/Mirc19<tm1.1Kcho>	B6.129-Mirc19<tm1.1Kcho>	N	21057503
MGI:4868377	F	MP:0009506	abnormal mammary gland alveolus morphology	Mirc19<tm1.1Kcho>/Mirc19<tm1.1Kcho>	B6.129-Mirc19<tm1.1Kcho>	N	21057503
MGI:4868377	F	MP:0005389	reproductive system phenotype	Mirc19<tm1.1Kcho>/Mirc19<tm1.1Kcho>	B6.129-Mirc19<tm1.1Kcho>	Y	21057503
MGI:4868377	F	MP:0006270	abnormal mammary gland growth during lactation	Mirc19<tm1.1Kcho>/Mirc19<tm1.1Kcho>	B6.129-Mirc19<tm1.1Kcho>	N	21057503
MGI:4868377	F	MP:0009503	abnormal mammary gland duct morphology	Mirc19<tm1.1Kcho>/Mirc19<tm1.1Kcho>	B6.129-Mirc19<tm1.1Kcho>	N	21057503
MGI:4868696	M	MP:0001925	male infertility	Nphp4<nmf192>/Nphp4<nmf192>	involves: C57BL/6J	N	21078623
MGI:4868696	M	MP:0002687	oligozoospermia	Nphp4<nmf192>/Nphp4<nmf192>	involves: C57BL/6J	N	21078623
MGI:4868696	M	MP:0002675	asthenozoospermia	Nphp4<nmf192>/Nphp4<nmf192>	involves: C57BL/6J	N	21078623
MGI:4878877	M	MP:0001147	small testis	Tert<tm2.1Rdp>/Tert<tm2.1Rdp>	involves: C57BL/6	N	21113150
MGI:4878877	M	MP:0003205	testicular atrophy	Tert<tm2.1Rdp>/Tert<tm2.1Rdp>	involves: C57BL/6	N	21113150
MGI:4878877	M	MP:0008280	abnormal male germ cell apoptosis	Tert<tm2.1Rdp>/Tert<tm2.1Rdp>	involves: C57BL/6	N	21113150
MGI:4878879	F	MP:0001927	abnormal estrous cycle	Esr1<tm1.2Awo>/Esr1<tm1.2Awo>,Kiss1<tm1.1(cre)Uboe>/Kiss1<+>	involves: 129S6/SvEvTac * C57BL/6 * SJL	N	21149719
MGI:4878879	F	MP:0002016	ovary cyst	Esr1<tm1.2Awo>/Esr1<tm1.2Awo>,Kiss1<tm1.1(cre)Uboe>/Kiss1<+>	involves: 129S6/SvEvTac * C57BL/6 * SJL	N	21149719
MGI:4878879	F	MP:0008994	early vaginal opening	Esr1<tm1.2Awo>/Esr1<tm1.2Awo>,Kiss1<tm1.1(cre)Uboe>/Kiss1<+>	involves: 129S6/SvEvTac * C57BL/6 * SJL	N	21149719
MGI:4878879	F	MP:0009011	prolonged diestrus	Esr1<tm1.2Awo>/Esr1<tm1.2Awo>,Kiss1<tm1.1(cre)Uboe>/Kiss1<+>	involves: 129S6/SvEvTac * C57BL/6 * SJL	N	21149719
MGI:4878879	M	MP:0005389	reproductive system phenotype	Esr1<tm1.2Awo>/Esr1<tm1.2Awo>,Kiss1<tm1.1(cre)Uboe>/Kiss1<+>	involves: 129S6/SvEvTac * C57BL/6 * SJL	Y	21149719
MGI:4878879	F	MP:0009444	ovarian follicular cyst	Esr1<tm1.2Awo>/Esr1<tm1.2Awo>,Kiss1<tm1.1(cre)Uboe>/Kiss1<+>	involves: 129S6/SvEvTac * C57BL/6 * SJL	N	21149719
MGI:4878879	F	MP:0001134	absent corpus luteum	Esr1<tm1.2Awo>/Esr1<tm1.2Awo>,Kiss1<tm1.1(cre)Uboe>/Kiss1<+>	involves: 129S6/SvEvTac * C57BL/6 * SJL	N	21149719
MGI:4879003	F	MP:0001552	increased circulating triglyceride level	Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>/Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL	N	21076408
MGI:4879003	F	MP:0000183	decreased circulating LDL cholesterol level	Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>/Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL	N	21076408
MGI:4879003	M	MP:0002079	increased circulating insulin level	Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>/Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL	N	21076408
MGI:4879003	F	MP:0001554	increased circulating free fatty acids level	Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>/Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL	N	21076408
MGI:4879003	F	MP:0001556	increased circulating HDL cholesterol level	Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>/Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL	N	21076408
MGI:4879004	F	MP:0001552	increased circulating triglyceride level	Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL	N	21076408
MGI:4879004	F	MP:0001556	increased circulating HDL cholesterol level	Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL	N	21076408
MGI:4879004	M	MP:0005669	increased circulating leptin level	Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL	N	21076408
MGI:4879004	F	MP:0000183	decreased circulating LDL cholesterol level	Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL	N	21076408
MGI:4879004	F	MP:0001554	increased circulating free fatty acids level	Gt(ROSA)26Sor<tm1.1(CAG-Fto)Rdc>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL	N	21076408
MGI:4879097	M	MP:0009233	enlarged sperm head	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0009839	multiflagellated sperm	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0002686	globozoospermia	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0005578	teratozoospermia	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0004852	decreased testis weight	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0002675	asthenozoospermia	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0004901	decreased male germ cell number	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0001152	increased Leydig cell number	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0008261	arrest of male meiosis	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0001154	seminiferous tubule degeneration	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0001147	small testis	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0009238	coiled sperm flagellum	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0020550	multinucleated giant male germ cells	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0001158	abnormal prostate gland morphology	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0001925	male infertility	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0002687	oligozoospermia	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879097	M	MP:0009239	short sperm flagellum	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>	involves: 129 * C57BL/6J * FVB/N	N	21124965
MGI:4879099	M	MP:0001154	seminiferous tubule degeneration	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>,Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129 * 129S7/SvEvBrd * C57BL/6J * FVB/N	N	21124965
MGI:4879099	M	MP:0004852	decreased testis weight	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>,Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129 * 129S7/SvEvBrd * C57BL/6J * FVB/N	N	21124965
MGI:4879099	M	MP:0002687	oligozoospermia	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>,Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129 * 129S7/SvEvBrd * C57BL/6J * FVB/N	N	21124965
MGI:4879099	M	MP:0001925	male infertility	Ing2<tm1.1Ccha>/Ing2<tm1.1Ccha>,Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129 * 129S7/SvEvBrd * C57BL/6J * FVB/N	N	21124965
MGI:4880766	F	MP:0001139	abnormal vagina morphology	Lhfpl2<vgim>/Lhfpl2<vgim>	B6(129S4)-Lhfpl2<vgim>/GrsrJ	N	MGI:4880664
MGI:4880766	F	MP:0001926	female infertility	Lhfpl2<vgim>/Lhfpl2<vgim>	B6(129S4)-Lhfpl2<vgim>/GrsrJ	N	MGI:4880664
MGI:4880766	F	MP:0001144	vagina atresia	Lhfpl2<vgim>/Lhfpl2<vgim>	B6(129S4)-Lhfpl2<vgim>/GrsrJ	N	MGI:4880664
MGI:4880766	F	MP:0001136	dilated uterine cervix	Lhfpl2<vgim>/Lhfpl2<vgim>	B6(129S4)-Lhfpl2<vgim>/GrsrJ	N	MGI:4880664
MGI:4880766	F	MP:0001120	abnormal uterus morphology	Lhfpl2<vgim>/Lhfpl2<vgim>	B6(129S4)-Lhfpl2<vgim>/GrsrJ	N	MGI:4880664
MGI:4880766	F	MP:0003531	abnormal vagina development	Lhfpl2<vgim>/Lhfpl2<vgim>	B6(129S4)-Lhfpl2<vgim>/GrsrJ	N	MGI:4880664
MGI:4880766	F	MP:0009208	abnormal female genitalia morphology	Lhfpl2<vgim>/Lhfpl2<vgim>	B6(129S4)-Lhfpl2<vgim>/GrsrJ	N	MGI:4880664
MGI:4881338	M	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology	Foxp3<sf>/Y	B6.Cg-Foxp3<sf>	N	12612578
MGI:4881338	M	MP:0002599	increased mean platelet volume	Foxp3<sf>/Y	B6.Cg-Foxp3<sf>	N	19661482
MGI:4881338	M	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	Foxp3<sf>/Y	B6.Cg-Foxp3<sf>	N	12612578
MGI:4881338	M	MP:0008255	decreased megakaryocyte cell number	Foxp3<sf>/Y	B6.Cg-Foxp3<sf>	N	19661482
MGI:4881338	M	MP:0001764	abnormal homeostasis	Foxp3<sf>/Y	B6.Cg-Foxp3<sf>	N	19661482
MGI:4881338	M	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology	Foxp3<sf>/Y	B6.Cg-Foxp3<sf>	N	12612578
MGI:4881338	M	MP:0003179	thrombocytopenia	Foxp3<sf>/Y	B6.Cg-Foxp3<sf>	N	19661482
MGI:4881338	M	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Foxp3<sf>/Y	B6.Cg-Foxp3<sf>	N	19661482
MGI:4881723	M	MP:0031426	increased sperm motility	Cnr1<tm1Map>/Cnr1<tm1Map>	involves: 129S1/Sv * 129X1/SvJ	N	17395184
MGI:4882032	F	MP:0009361	abnormal primordial ovarian follicle morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Gdf9-icre)5092Coo/0	involves: 129S4/SvJae * C57BL/6	N	19587782
MGI:4882101	M	MP:0004359	short ulna	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0004686	decreased length of long bones	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0002764	short tibia	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0005296	abnormal humerus morphology	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0004355	short radius	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0006396	decreased long bone epiphyseal plate size	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0003109	short femur	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0011261	abnormal limb mesenchyme morphology	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0002082	postnatal lethality	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0000562	polydactyly	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0000564	syndactyly	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0009780	abnormal chondrocyte physiology	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0002896	abnormal bone mineralization	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0004351	short humerus	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0003055	abnormal long bone epiphyseal plate morphology	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0002765	short fibula	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882101	M	MP:0004214	abnormal long bone diaphysis morphology	Ofd1<tm2.1Bfra>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882102	F	MP:0003109	short femur	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882102	F	MP:0006279	abnormal limb development	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882102	F	MP:0004355	short radius	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882102	F	MP:0002764	short tibia	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882102	F	MP:0004359	short ulna	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882102	F	MP:0004351	short humerus	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882102	F	MP:0002765	short fibula	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882102	F	MP:0011261	abnormal limb mesenchyme morphology	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882102	F	MP:0009743	preaxial polydactyly	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882102	F	MP:0005296	abnormal humerus morphology	Ofd1<tm2.1Bfra>/Ofd1<+>,Tg(Prrx1-cre)1Cjt/0	involves: 129S2/SvPas * C57BL/6J * SJL/J	N	20920500
MGI:4882103	F	MP:0004355	short radius	Ofd1<tm1Bfra>/Ofd1<tm1Bfra>	involves: 129S2/SvPas	N	20920500
MGI:4882103	F	MP:0011261	abnormal limb mesenchyme morphology	Ofd1<tm1Bfra>/Ofd1<tm1Bfra>	involves: 129S2/SvPas	N	20920500
MGI:4882104	M	MP:0005371	limbs/digits/tail phenotype	Ofd1<tm2.1Bfra>/Y,Tg(Msx2-cre)5Rem/0	involves: 129S2/SvPas	Y	20920500
MGI:4882147	F	MP:0003507	abnormal ovary physiology	Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Tg(Ddx4-cre)1Dcas/0	involves: 129S6/SvEvTac * FVB/N	N	18601916
MGI:4882147	F	MP:0004832	enlarged ovary	Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Tg(Ddx4-cre)1Dcas/0	involves: 129S6/SvEvTac * FVB/N	N	18601916
MGI:4882147	F	MP:0009361	abnormal primordial ovarian follicle morphology	Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Tg(Ddx4-cre)1Dcas/0	involves: 129S6/SvEvTac * FVB/N	N	18601916
MGI:4882148	F	MP:0003507	abnormal ovary physiology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * FVB/N	N	18601916
MGI:4882148	F	MP:0004832	enlarged ovary	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * FVB/N	N	18601916
MGI:4882148	F	MP:0001923	reduced female fertility	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * FVB/N	N	18601916
MGI:4882149	F	MP:0009361	abnormal primordial ovarian follicle morphology	Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Tg(Ddx4-cre/ERT2)1Dcas/0	involves: 129S6/SvEvTac * FVB/N	N	18601916
MGI:4882149	F	MP:0004832	enlarged ovary	Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Tg(Ddx4-cre/ERT2)1Dcas/0	involves: 129S6/SvEvTac * FVB/N	N	18601916
MGI:4882150	F	MP:0004832	enlarged ovary	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Ddx4-cre/ERT2)1Dcas/0	involves: 129S4/SvJae * FVB/N	N	18601916
MGI:4882150	F	MP:0009361	abnormal primordial ovarian follicle morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Ddx4-cre/ERT2)1Dcas/0	involves: 129S4/SvJae * FVB/N	N	18601916
MGI:4887234	F	MP:0001120	abnormal uterus morphology	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Wnt7a-EGFP/cre)#Bhr/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	20974921
MGI:4887234	F	MP:0009662	abnormal uterine receptivity	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Wnt7a-EGFP/cre)#Bhr/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	20974921
MGI:4887234	F	MP:0004902	abnormal uterus size	Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Wnt7a-EGFP/cre)#Bhr/0	involves: 129S2/SvPas * C57BL/6 * SJL	N	20974921
MGI:4887243	M	MP:0014052	increased male germ cell apoptosis	Hormad1<tm1Rajk>/Hormad1<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	21079677
MGI:4887243	M	MP:0001154	seminiferous tubule degeneration	Hormad1<tm1Rajk>/Hormad1<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	21079677
MGI:4887243	F	MP:0001728	failure of embryo implantation	Hormad1<tm1Rajk>/Hormad1<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	21079677
MGI:4887243	M	MP:0005159	azoospermia	Hormad1<tm1Rajk>/Hormad1<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	21079677
MGI:4887243	F	MP:0001926	female infertility	Hormad1<tm1Rajk>/Hormad1<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	21079677
MGI:4887243	M	MP:0001146	abnormal testis morphology	Hormad1<tm1Rajk>/Hormad1<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	21079677
MGI:4887243	M	MP:0004852	decreased testis weight	Hormad1<tm1Rajk>/Hormad1<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	21079677
MGI:4887243	M	MP:0001925	male infertility	Hormad1<tm1Rajk>/Hormad1<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	21079677
MGI:4887243	F	MP:0014445	abnormal spindle assembly in female meiosis	Hormad1<tm1Rajk>/Hormad1<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	21079677
MGI:4887243	M	MP:0001147	small testis	Hormad1<tm1Rajk>/Hormad1<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	21079677
MGI:4887243	F	MP:0010767	abnormal female meiosis I arrest	Hormad1<tm1Rajk>/Hormad1<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	21079677
MGI:4887243	M	MP:0008261	arrest of male meiosis	Hormad1<tm1Rajk>/Hormad1<tm1Rajk>	involves: 129S7/SvEvBrd * C57BL/6	N	21079677
MGI:4887441	F	MP:0008722	abnormal chemokine secretion	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887441	F	MP:0008560	increased tumor necrosis factor secretion	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887441	F	MP:0003156	abnormal leukocyte migration	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887441	F	MP:0005617	increased susceptibility to type IV hypersensitivity reaction	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887441	F	MP:0005399	increased susceptibility to fungal infection	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887441	F	MP:0008566	increased interferon-gamma secretion	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887441	F	MP:0003009	abnormal cytokine secretion	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887441	F	MP:0008687	increased interleukin-2 secretion	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887441	F	MP:0008699	increased interleukin-4 secretion	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887441	F	MP:0008663	increased interleukin-12 secretion	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887441	F	MP:0005547	abnormal Muller cell morphology	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887441	F	MP:0008660	increased interleukin-10 secretion	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887441	F	MP:0000952	abnormal CNS glial cell morphology	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887441	F	MP:0008702	increased interleukin-5 secretion	Gpr34<tm1.1Shbg>/Gpr34<tm1.1Shbg>	B6.Cg-Gpr34<tm1.1Shbg>	N	21097509
MGI:4887824	F	MP:0001194	dermatitis	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>,Mir146<tm1.1Bal>/Mir146<tm1.1Bal>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	20850013
MGI:4887824	F	MP:0005251	blepharitis	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>,Mir146<tm1.1Bal>/Mir146<tm1.1Bal>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	20850013
MGI:4887824	F	MP:0008567	decreased interferon-gamma secretion	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>,Mir146<tm1.1Bal>/Mir146<tm1.1Bal>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	20850013
MGI:4887824	F	MP:0004973	increased regulatory T cell number	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>,Mir146<tm1.1Bal>/Mir146<tm1.1Bal>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	20850013
MGI:4887824	F	MP:0001852	conjunctivitis	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>,Mir146<tm1.1Bal>/Mir146<tm1.1Bal>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	20850013
MGI:4887824	F	MP:0003786	premature aging	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>,Mir146<tm1.1Bal>/Mir146<tm1.1Bal>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	20850013
MGI:4887824	F	MP:0003945	abnormal lymphocyte physiology	Foxp3<tm1.1Ayr>/Foxp3<tm1.1Ayr>,Mir146<tm1.1Bal>/Mir146<tm1.1Bal>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	20850013
MGI:4887825	F	MP:0001852	conjunctivitis	Socs1<tm1Ayos>/Socs1<tm1Ayos>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	20850013
MGI:4887825	F	MP:0004973	increased regulatory T cell number	Socs1<tm1Ayos>/Socs1<tm1Ayos>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	20850013
MGI:4887825	F	MP:0005251	blepharitis	Socs1<tm1Ayos>/Socs1<tm1Ayos>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	20850013
MGI:4887825	F	MP:0001194	dermatitis	Socs1<tm1Ayos>/Socs1<tm1Ayos>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	20850013
MGI:4887830	F	MP:0001412	excessive scratching	Grpr<tm1Jfb>/Grpr<tm1Jfb>,Slc17a6<tm1Kldr>/Slc17a6<tm1Kldr>,Th<tm1(cre)Te>/Th<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21040852
MGI:4887942	M	MP:0002412	increased susceptibility to bacterial infection	Il2rg<tm1.1Flv>/Y,Rag2<tm1.1Flv>/Rag2<tm1.1Flv>	involves: 129S4/SvJae * BALB/cAnNTac	N	20951970
MGI:4887942	M	MP:0005671	abnormal response to transplant	Il2rg<tm1.1Flv>/Y,Rag2<tm1.1Flv>/Rag2<tm1.1Flv>	involves: 129S4/SvJae * BALB/cAnNTac	N	20951970
MGI:4887944	F	MP:0005671	abnormal response to transplant	Il2rg<tm1.1Flv>/Il2rg<tm1.1Flv>,Rag2<tm1.1Flv>/Rag2<tm1.1Flv>	involves: 129S4/SvJae * BALB/cAnNTac	N	20951970
MGI:4887944	F	MP:0002412	increased susceptibility to bacterial infection	Il2rg<tm1.1Flv>/Il2rg<tm1.1Flv>,Rag2<tm1.1Flv>/Rag2<tm1.1Flv>	involves: 129S4/SvJae * BALB/cAnNTac	N	20951970
MGI:4887947	F	MP:0003179	thrombocytopenia	Il2rg<tm1.1Flv>/Il2rg<tm1.1Flv>,Rag2<tm1.1Flv>/Rag2<tm1.1Flv>,Thpo<tm1.1(TPO)Flv>/Thpo<tm1.1(TPO)Flv>	involves: 129S4/SvJae * BALB/cAnNTac	N	21262827
MGI:4887947	F	MP:0005671	abnormal response to transplant	Il2rg<tm1.1Flv>/Il2rg<tm1.1Flv>,Rag2<tm1.1Flv>/Rag2<tm1.1Flv>,Thpo<tm1.1(TPO)Flv>/Thpo<tm1.1(TPO)Flv>	involves: 129S4/SvJae * BALB/cAnNTac	N	21262827
MGI:4887950	F	MP:0005671	abnormal response to transplant	Il2rg<tm1.1Flv>/Il2rg<tm1.1Flv>,Csf2/Il3<tm1.1(CSF2,IL3)Flv>/Csf2/Il3<tm1.1(CSF2,IL3)Flv>,Rag2<tm1.1Flv>/Rag2<tm1.1Flv>	involves: 129S4/SvJae * BALB/cAnNCr * BALB/cAnNTac	N	21262803
MGI:4887951	F	MP:0005671	abnormal response to transplant	Csf2/Il3<tm1.1(CSF2,IL3)Flv>/Csf2/Il3<tm1.1(CSF2,IL3)Flv>,Il2rg<tm1.1Flv>/Il2rg<tm1.1Flv>,Rag2<tm1.1Flv>/Rag2<tm1.1Flv>	involves: 129S4/SvJae * BALB/cAnNCr * BALB/cAnNTac	N	21262803
MGI:4888413	F	MP:0031434	increased miscarriage rate	Itgb3<tm1Hyn>/Itgb3<tm1Hyn>	involves: 129S2/SvPas * BALB/c	N	16317099
MGI:4888635	F	MP:0006270	abnormal mammary gland growth during lactation	Tg(MMTV-cre)4Mam/?	involves: FVB	N	21255551
MGI:4888636	F	MP:0006270	abnormal mammary gland growth during lactation	Tg(MMTV-cre)1Mam/?	involves: FVB	N	21255551
MGI:4888637	F	MP:0006270	abnormal mammary gland growth during lactation	Tg(MMTV-cre)FMam/?	involves: FVB	N	21255551
MGI:4889051	M	MP:0010233	hairless tail	Eda<Ta-By>/Y	involves: BALB/cBy	N	MGI:78592
MGI:4889051	M	MP:0006365	absent guard hair	Eda<Ta-By>/Y	involves: BALB/cBy	N	MGI:78592
MGI:4889051	M	MP:0005287	narrow eye opening	Eda<Ta-By>/Y	involves: BALB/cBy	N	MGI:78592
MGI:4889051	M	MP:0002111	abnormal tail morphology	Eda<Ta-By>/Y	involves: BALB/cBy	N	MGI:78592
MGI:4889051	M	MP:0002073	abnormal hair growth	Eda<Ta-By>/Y	involves: BALB/cBy	N	MGI:78592
MGI:4889051	M	MP:0000585	kinked tail	Eda<Ta-By>/Y	involves: BALB/cBy	N	MGI:78592
MGI:4889052	F	MP:0002074	abnormal hair texture	Eda<Ta-By>/Eda<+>	involves: BALB/cBy	N	MGI:78592
MGI:4889052	F	MP:0001510	abnormal coat appearance	Eda<Ta-By>/Eda<+>	involves: BALB/cBy	N	MGI:78592
MGI:4889107	F	MP:0001473	reduced long-term potentiation	Atrx<tm1Enl>/Atrx<tm1Enl>	B6.129S4-Atrx<tm1Enl>	N	20865721
MGI:4889107	F	MP:0009454	impaired contextual conditioning behavior	Atrx<tm1Enl>/Atrx<tm1Enl>	B6.129S4-Atrx<tm1Enl>	N	20865721
MGI:4889107	F	MP:0001262	decreased body weight	Atrx<tm1Enl>/Atrx<tm1Enl>	B6.129S4-Atrx<tm1Enl>	N	20865721
MGI:4889107	F	MP:0011101	prenatal lethality, incomplete penetrance	Atrx<tm1Enl>/Atrx<tm1Enl>	B6.129S4-Atrx<tm1Enl>	N	20865721
MGI:4889107	F	MP:0005386	behavior/neurological phenotype	Atrx<tm1Enl>/Atrx<tm1Enl>	B6.129S4-Atrx<tm1Enl>	Y	20865721
MGI:4889120	F	MP:0006270	abnormal mammary gland growth during lactation	Pygo2<tm1.1Xdai>/Pygo2<tm1.2Xdai>,Tg(KRT14-cre)#Smr/0	involves: 129P2/OlaHsd * C57BL/6J * SJL/J	N	19487454
MGI:4889120	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Pygo2<tm1.1Xdai>/Pygo2<tm1.2Xdai>,Tg(KRT14-cre)#Smr/0	involves: 129P2/OlaHsd * C57BL/6J * SJL/J	N	19487454
MGI:4889120	F	MP:0004135	abnormal mammary gland embryonic development	Pygo2<tm1.1Xdai>/Pygo2<tm1.2Xdai>,Tg(KRT14-cre)#Smr/0	involves: 129P2/OlaHsd * C57BL/6J * SJL/J	N	19487454
MGI:4889120	F	MP:0010249	lactation failure	Pygo2<tm1.1Xdai>/Pygo2<tm1.2Xdai>,Tg(KRT14-cre)#Smr/0	involves: 129P2/OlaHsd * C57BL/6J * SJL/J	N	19487454
MGI:4889120	F	MP:0000662	abnormal branching of the mammary ductal tree	Pygo2<tm1.1Xdai>/Pygo2<tm1.2Xdai>,Tg(KRT14-cre)#Smr/0	involves: 129P2/OlaHsd * C57BL/6J * SJL/J	N	19487454
MGI:4889120	F	MP:0000628	abnormal mammary gland development	Pygo2<tm1.1Xdai>/Pygo2<tm1.2Xdai>,Tg(KRT14-cre)#Smr/0	involves: 129P2/OlaHsd * C57BL/6J * SJL/J	N	19487454
MGI:4889120	F	MP:0006269	abnormal mammary gland growth during pregnancy	Pygo2<tm1.1Xdai>/Pygo2<tm1.2Xdai>,Tg(KRT14-cre)#Smr/0	involves: 129P2/OlaHsd * C57BL/6J * SJL/J	N	19487454
MGI:4889121	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Pygo2<tm1.2Xdai>/Pygo2<tm1.2Xdai>	involves: 129P2/OlaHsd	N	19487454
MGI:4889203	F	MP:0001923	reduced female fertility	Fst<tm1Alsc>/Fst<tm1Alsc>	Not Specified	N	20032047
MGI:4889203	F	MP:0031239	increased atretic ovarian follicle number	Fst<tm1Alsc>/Fst<tm1Alsc>	Not Specified	N	20032047
MGI:4889203	F	MP:0011124	increased primary ovarian follicle number	Fst<tm1Alsc>/Fst<tm1Alsc>	Not Specified	N	20032047
MGI:4889203	F	MP:0031383	increased secondary ovarian follicle number	Fst<tm1Alsc>/Fst<tm1Alsc>	Not Specified	N	20032047
MGI:4889203	F	MP:0011129	decreased tertiary ovarian follicle number	Fst<tm1Alsc>/Fst<tm1Alsc>	Not Specified	N	20032047
MGI:4889203	F	MP:0009361	abnormal primordial ovarian follicle morphology	Fst<tm1Alsc>/Fst<tm1Alsc>	Not Specified	N	20032047
MGI:4889211	F	MP:0005425	increased macrophage cell number	Cmah<tm1Avrk>/Cmah<tm1Avrk>,Dmd<mdx>/Dmd<mdx>	involves: 129X1/SvJ * C57BL/10ScSn	N	20668298
MGI:4889211	F	MP:0002083	premature death	Cmah<tm1Avrk>/Cmah<tm1Avrk>,Dmd<mdx>/Dmd<mdx>	involves: 129X1/SvJ * C57BL/10ScSn	N	20668298
MGI:4889211	F	MP:0000747	muscle weakness	Cmah<tm1Avrk>/Cmah<tm1Avrk>,Dmd<mdx>/Dmd<mdx>	involves: 129X1/SvJ * C57BL/10ScSn	N	20668298
MGI:4889211	F	MP:0001406	abnormal gait	Cmah<tm1Avrk>/Cmah<tm1Avrk>,Dmd<mdx>/Dmd<mdx>	involves: 129X1/SvJ * C57BL/10ScSn	N	20668298
MGI:4889211	F	MP:0000752	dystrophic muscle	Cmah<tm1Avrk>/Cmah<tm1Avrk>,Dmd<mdx>/Dmd<mdx>	involves: 129X1/SvJ * C57BL/10ScSn	N	20668298
MGI:4889211	F	MP:0009419	skeletal muscle fibrosis	Cmah<tm1Avrk>/Cmah<tm1Avrk>,Dmd<mdx>/Dmd<mdx>	involves: 129X1/SvJ * C57BL/10ScSn	N	20668298
MGI:4889211	F	MP:0000220	increased monocyte cell number	Cmah<tm1Avrk>/Cmah<tm1Avrk>,Dmd<mdx>/Dmd<mdx>	involves: 129X1/SvJ * C57BL/10ScSn	N	20668298
MGI:4889211	F	MP:0010632	cardiac muscle necrosis	Cmah<tm1Avrk>/Cmah<tm1Avrk>,Dmd<mdx>/Dmd<mdx>	involves: 129X1/SvJ * C57BL/10ScSn	N	20668298
MGI:4889211	F	MP:0001405	impaired coordination	Cmah<tm1Avrk>/Cmah<tm1Avrk>,Dmd<mdx>/Dmd<mdx>	involves: 129X1/SvJ * C57BL/10ScSn	N	20668298
MGI:4936861	M	MP:0001148	enlarged testis	Sptbn1<tm1Mish>/Sptbn1<+>	involves: 129S6/SvEvTac	N	20739274
MGI:4936861	F	MP:0008000	increased ovary tumor incidence	Sptbn1<tm1Mish>/Sptbn1<+>	involves: 129S6/SvEvTac	N	20739274
MGI:4936861	M	MP:0006262	increased testis tumor incidence	Sptbn1<tm1Mish>/Sptbn1<+>	involves: 129S6/SvEvTac	N	20739274
MGI:4936865	M	MP:0000759	abnormal skeletal muscle morphology	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0000752	dystrophic muscle	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0003852	skeletal muscle necrosis	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0004510	myositis	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0002269	muscular atrophy	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0012106	impaired exercise endurance	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0003833	decreased satellite cell number	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0010090	increased circulating creatine kinase level	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0009403	increased variability of skeletal muscle fiber size	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0009419	skeletal muscle fibrosis	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0002106	abnormal muscle physiology	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0000160	kyphosis	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0030927	decreased telomere length	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0000747	muscle weakness	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0003199	calcified muscle	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0009415	skeletal muscle degeneration	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0004145	abnormal muscle electrophysiology	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0001953	respiratory failure	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0008866	chromosomal instability	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0002279	abnormal diaphragm morphology	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936865	M	MP:0002083	premature death	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<tm1Rdp>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936867	M	MP:0002279	abnormal diaphragm morphology	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<+>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936867	M	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<+>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936867	M	MP:0002106	abnormal muscle physiology	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<+>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4936867	M	MP:0010090	increased circulating creatine kinase level	Dmd<mdx>/Y,Terc<tm1Rdp>/Terc<+>	involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	N	21145579
MGI:4938269	M	MP:0001156	abnormal spermatogenesis	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slx4<tm1a(EUCOMM)Wtsi>	N	21240276
MGI:4938269	F	MP:0001132	absent mature ovarian follicles	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slx4<tm1a(EUCOMM)Wtsi>	N	21240276
MGI:4938269	F	MP:0001923	reduced female fertility	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slx4<tm1a(EUCOMM)Wtsi>	N	21240276
MGI:4938269	M	MP:0005159	azoospermia	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slx4<tm1a(EUCOMM)Wtsi>	N	21240276
MGI:4938269	F	MP:0001134	absent corpus luteum	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slx4<tm1a(EUCOMM)Wtsi>	N	21240276
MGI:4938269	M	MP:0008280	abnormal male germ cell apoptosis	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slx4<tm1a(EUCOMM)Wtsi>	N	21240276
MGI:4938269	M	MP:0001922	reduced male fertility	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slx4<tm1a(EUCOMM)Wtsi>	N	21240276
MGI:4938269	F	MP:0004805	absent oocytes	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slx4<tm1a(EUCOMM)Wtsi>	N	21240276
MGI:4938269	M	MP:0002687	oligozoospermia	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slx4<tm1a(EUCOMM)Wtsi>	N	21240276
MGI:4938615	M	MP:0002169	no abnormal phenotype detected	Mecp2<tm3.1Bird>/Y	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6	N	MGI:4938312
MGI:4938616	F	MP:0002169	no abnormal phenotype detected	Mecp2<tm3.1Bird>/Mecp2<tm3.1Bird>	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6	N	MGI:4938312
MGI:4939585	M	MP:0005578	teratozoospermia	Elovl2<tm1Jaco>/Elovl2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21106902
MGI:4939585	M	MP:0001922	reduced male fertility	Elovl2<tm1Jaco>/Elovl2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21106902
MGI:4939585	M	MP:0009230	abnormal sperm head morphology	Elovl2<tm1Jaco>/Elovl2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21106902
MGI:4939586	M	MP:0001155	arrest of spermatogenesis	Elovl2<tm1Jaco>/Elovl2<tm1Jaco>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21106902
MGI:4939586	M	MP:0004852	decreased testis weight	Elovl2<tm1Jaco>/Elovl2<tm1Jaco>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21106902
MGI:4939586	M	MP:0001925	male infertility	Elovl2<tm1Jaco>/Elovl2<tm1Jaco>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21106902
MGI:4940051	M	MP:0000755	hindlimb paralysis	Atp7a<Mo-ms>/Y	Not Specified	N	20831904
MGI:4940051	M	MP:0003203	increased neuron apoptosis	Atp7a<Mo-ms>/Y	Not Specified	N	19375486
MGI:4940051	M	MP:0011085	postnatal lethality, complete penetrance	Atp7a<Mo-ms>/Y	Not Specified	N	MGI:63205
MGI:4940051	M	MP:0000745	tremors	Atp7a<Mo-ms>/Y	Not Specified	N	20831904
MGI:4940051	M	MP:0011215	decreased brain copper level	Atp7a<Mo-ms>/Y	Not Specified	N	20831904
MGI:4940051	M	MP:0003952	abnormal copper level	Atp7a<Mo-ms>/Y	Not Specified	N	20831904
MGI:4940051	M	MP:0002098	abnormal vibrissa morphology	Atp7a<Mo-ms>/Y	Not Specified	N	MGI:63205
MGI:4940051	M	MP:0000371	diluted coat color	Atp7a<Mo-ms>/Y	Not Specified	N	MGI:63205
MGI:4940051	M	MP:0001274	curly vibrissae	Atp7a<Mo-ms>/Y	Not Specified	N	MGI:63205
MGI:4940051	M	MP:0001393	ataxia	Atp7a<Mo-ms>/Y	Not Specified	N	20831904
MGI:4940051	M	MP:0003067	decreased liver copper level	Atp7a<Mo-ms>/Y	Not Specified	N	20831904
MGI:4940051	M	MP:0010243	increased kidney copper level	Atp7a<Mo-ms>/Y	Not Specified	N	20831904
MGI:4940052	M	MP:0004505	decreased renal glomerulus number	Atp7a<Mo-ms>/Y	involves: CBA	N	11534785
MGI:4940052	M	MP:0002703	abnormal renal tubule morphology	Atp7a<Mo-ms>/Y	involves: CBA	N	11534785
MGI:4940052	M	MP:0003918	decreased kidney weight	Atp7a<Mo-ms>/Y	involves: CBA	N	11534785
MGI:4940052	M	MP:0010243	increased kidney copper level	Atp7a<Mo-ms>/Y	involves: CBA	N	11534785
MGI:4940053	F	MP:0001274	curly vibrissae	Atp7a<Mo-ms>/Atp7a<+>	Not Specified	N	MGI:63205
MGI:4940053	F	MP:0000367	abnormal coat/ hair morphology	Atp7a<Mo-ms>/Atp7a<+>	Not Specified	N	MGI:63205
MGI:4940054	M	MP:0011215	decreased brain copper level	Atp7a<Mo-ms>/Y	involves: CBA/Kw	N	MGI:63033
MGI:4940054	M	MP:0012661	decreased circulating ceruloplasmin level	Atp7a<Mo-ms>/Y	involves: CBA/Kw	N	MGI:63033
MGI:4940054	M	MP:0003951	abnormal copper homeostasis	Atp7a<Mo-ms>/Y	involves: CBA/Kw	N	MGI:63033
MGI:4940054	M	MP:0001274	curly vibrissae	Atp7a<Mo-ms>/Y	involves: CBA/Kw	N	MGI:63033
MGI:4940054	M	MP:0003067	decreased liver copper level	Atp7a<Mo-ms>/Y	involves: CBA/Kw	N	MGI:63033
MGI:4940054	M	MP:0031204	hindlimb paresis	Atp7a<Mo-ms>/Y	involves: CBA/Kw	N	MGI:63033
MGI:4940054	M	MP:0010247	increased intestine copper level	Atp7a<Mo-ms>/Y	involves: CBA/Kw	N	MGI:63033
MGI:4940054	M	MP:0001263	weight loss	Atp7a<Mo-ms>/Y	involves: CBA/Kw	N	MGI:63033
MGI:4940054	M	MP:0000402	abnormal zigzag hair morphology	Atp7a<Mo-ms>/Y	involves: CBA/Kw	N	MGI:63033
MGI:4940054	M	MP:0000400	abnormal awl hair morphology	Atp7a<Mo-ms>/Y	involves: CBA/Kw	N	MGI:63033
MGI:4940054	M	MP:0011085	postnatal lethality, complete penetrance	Atp7a<Mo-ms>/Y	involves: CBA/Kw	N	MGI:63033
MGI:4940318	F	MP:0009412	skeletal muscle fiber degeneration	Dmd<mdx>/Dmd<mdx>,Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas * C57BL/6 * C57BL/10ScSn	N	20371627
MGI:4940318	F	MP:0010053	decreased grip strength	Dmd<mdx>/Dmd<mdx>,Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas * C57BL/6 * C57BL/10ScSn	N	20371627
MGI:4940318	F	MP:0010239	decreased skeletal muscle weight	Dmd<mdx>/Dmd<mdx>,Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas * C57BL/6 * C57BL/10ScSn	N	20371627
MGI:4940318	F	MP:0001265	decreased body size	Dmd<mdx>/Dmd<mdx>,Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas * C57BL/6 * C57BL/10ScSn	N	20371627
MGI:4940318	F	MP:0000752	dystrophic muscle	Dmd<mdx>/Dmd<mdx>,Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas * C57BL/6 * C57BL/10ScSn	N	20371627
MGI:4940318	F	MP:0009402	decreased skeletal muscle fiber diameter	Dmd<mdx>/Dmd<mdx>,Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas * C57BL/6 * C57BL/10ScSn	N	20371627
MGI:4940318	F	MP:0004510	myositis	Dmd<mdx>/Dmd<mdx>,Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas * C57BL/6 * C57BL/10ScSn	N	20371627
MGI:4940318	F	MP:0009400	decreased skeletal muscle fiber size	Dmd<mdx>/Dmd<mdx>,Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas * C57BL/6 * C57BL/10ScSn	N	20371627
MGI:4940318	F	MP:0001262	decreased body weight	Dmd<mdx>/Dmd<mdx>,Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas * C57BL/6 * C57BL/10ScSn	N	20371627
MGI:4941051	M	MP:0005578	teratozoospermia	Atp1a4<tm1Itl>/Atp1a4<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	21187400
MGI:4941051	M	MP:0002675	asthenozoospermia	Atp1a4<tm1Itl>/Atp1a4<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	21187400
MGI:4941051	M	MP:0009237	kinked sperm flagellum	Atp1a4<tm1Itl>/Atp1a4<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	21187400
MGI:4941051	M	MP:0004543	abnormal sperm physiology	Atp1a4<tm1Itl>/Atp1a4<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	21187400
MGI:4941051	M	MP:0001925	male infertility	Atp1a4<tm1Itl>/Atp1a4<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	21187400
MGI:4941051	M	MP:0003666	impaired sperm capacitation	Atp1a4<tm1Itl>/Atp1a4<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6	N	21187400
MGI:4941052	M	MP:0002675	asthenozoospermia	Atp1a4<tm1Itl>/Atp1a4<+>	involves: 129S6/SvEvTac * C57BL/6	N	21187400
MGI:4941159	F	MP:0010172	abnormal mammary gland epithelium physiology	Gt(ROSA)26Sor<tm1(Myc)Rcse>/Gt(ROSA)26Sor<tm1(Myc)Rcse>,Tg(Wap-cre)11738Mam/0	involves: 129 * C57BL/6 * SJL	N	21266350
MGI:4941159	F	MP:0014126	increased mammary gland apoptosis	Gt(ROSA)26Sor<tm1(Myc)Rcse>/Gt(ROSA)26Sor<tm1(Myc)Rcse>,Tg(Wap-cre)11738Mam/0	involves: 129 * C57BL/6 * SJL	N	21266350
MGI:4941159	F	MP:0000662	abnormal branching of the mammary ductal tree	Gt(ROSA)26Sor<tm1(Myc)Rcse>/Gt(ROSA)26Sor<tm1(Myc)Rcse>,Tg(Wap-cre)11738Mam/0	involves: 129 * C57BL/6 * SJL	N	21266350
MGI:4941160	F	MP:0000630	mammary gland hyperplasia	Gt(ROSA)26Sor<tm2(myc*T58A)Rcse>/Gt(ROSA)26Sor<tm2(myc*T58A)Rcse>,Tg(Wap-cre)11738Mam/0	involves: 129 * C57BL/6 * SJL	N	21266350
MGI:4941160	F	MP:0001884	mammary gland alveolar hyperplasia	Gt(ROSA)26Sor<tm2(myc*T58A)Rcse>/Gt(ROSA)26Sor<tm2(myc*T58A)Rcse>,Tg(Wap-cre)11738Mam/0	involves: 129 * C57BL/6 * SJL	N	21266350
MGI:4941160	F	MP:0006271	abnormal involution of the mammary gland	Gt(ROSA)26Sor<tm2(myc*T58A)Rcse>/Gt(ROSA)26Sor<tm2(myc*T58A)Rcse>,Tg(Wap-cre)11738Mam/0	involves: 129 * C57BL/6 * SJL	N	21266350
MGI:4941160	F	MP:0000662	abnormal branching of the mammary ductal tree	Gt(ROSA)26Sor<tm2(myc*T58A)Rcse>/Gt(ROSA)26Sor<tm2(myc*T58A)Rcse>,Tg(Wap-cre)11738Mam/0	involves: 129 * C57BL/6 * SJL	N	21266350
MGI:4941160	F	MP:0010172	abnormal mammary gland epithelium physiology	Gt(ROSA)26Sor<tm2(myc*T58A)Rcse>/Gt(ROSA)26Sor<tm2(myc*T58A)Rcse>,Tg(Wap-cre)11738Mam/0	involves: 129 * C57BL/6 * SJL	N	21266350
MGI:4941160	F	MP:0009506	abnormal mammary gland alveolus morphology	Gt(ROSA)26Sor<tm2(myc*T58A)Rcse>/Gt(ROSA)26Sor<tm2(myc*T58A)Rcse>,Tg(Wap-cre)11738Mam/0	involves: 129 * C57BL/6 * SJL	N	21266350
MGI:4941161	F	MP:0009506	abnormal mammary gland alveolus morphology	Gt(ROSA)26Sor<tm3(myc*S62A)Rcse>/Gt(ROSA)26Sor<tm3(myc*S62A)Rcse>,Tg(Wap-cre)11738Mam/0	involves: 129 * C57BL/6 * SJL	N	21266350
MGI:4941161	F	MP:0000662	abnormal branching of the mammary ductal tree	Gt(ROSA)26Sor<tm3(myc*S62A)Rcse>/Gt(ROSA)26Sor<tm3(myc*S62A)Rcse>,Tg(Wap-cre)11738Mam/0	involves: 129 * C57BL/6 * SJL	N	21266350
MGI:4941332	M	MP:0001157	small seminal vesicle	Lhx3<tm1.1Sjr>/Lhx3<tm1.1Sjr>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	21149718
MGI:4941332	F	MP:0003572	abnormal uterus development	Lhx3<tm1.1Sjr>/Lhx3<tm1.1Sjr>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	21149718
MGI:4941332	M	MP:0005159	azoospermia	Lhx3<tm1.1Sjr>/Lhx3<tm1.1Sjr>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	21149718
MGI:4941332	F	MP:0001120	abnormal uterus morphology	Lhx3<tm1.1Sjr>/Lhx3<tm1.1Sjr>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	21149718
MGI:4941332	F	MP:0002637	small uterus	Lhx3<tm1.1Sjr>/Lhx3<tm1.1Sjr>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	21149718
MGI:4941332	M	MP:0001147	small testis	Lhx3<tm1.1Sjr>/Lhx3<tm1.1Sjr>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	21149718
MGI:4941332	M	MP:0001156	abnormal spermatogenesis	Lhx3<tm1.1Sjr>/Lhx3<tm1.1Sjr>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	21149718
MGI:4941332	F	MP:0001926	female infertility	Lhx3<tm1.1Sjr>/Lhx3<tm1.1Sjr>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	21149718
MGI:4941332	M	MP:0002774	small prostate gland	Lhx3<tm1.1Sjr>/Lhx3<tm1.1Sjr>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	21149718
MGI:4941332	M	MP:0001938	delayed sexual maturation	Lhx3<tm1.1Sjr>/Lhx3<tm1.1Sjr>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	21149718
MGI:4941332	F	MP:0004905	decreased uterus weight	Lhx3<tm1.1Sjr>/Lhx3<tm1.1Sjr>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	21149718
MGI:4941332	M	MP:0001922	reduced male fertility	Lhx3<tm1.1Sjr>/Lhx3<tm1.1Sjr>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	21149718
MGI:4941332	M	MP:0009205	abnormal internal male genitalia morphology	Lhx3<tm1.1Sjr>/Lhx3<tm1.1Sjr>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	21149718
MGI:4941735	F	MP:0001923	reduced female fertility	Tsc1<tm1Djk>/Tsc1<tm1Djk>,Tg(Gdf9-icre)5092Coo/?	involves: 129S4/SvJae * C57BL/6J	N	19843540
MGI:4941735	F	MP:0031020	premature ovarian failure	Tsc1<tm1Djk>/Tsc1<tm1Djk>,Tg(Gdf9-icre)5092Coo/?	involves: 129S4/SvJae * C57BL/6J	N	19843540
MGI:4941735	F	MP:0001131	abnormal ovarian follicle morphology	Tsc1<tm1Djk>/Tsc1<tm1Djk>,Tg(Gdf9-icre)5092Coo/?	involves: 129S4/SvJae * C57BL/6J	N	19843540
MGI:4941739	F	MP:0009361	abnormal primordial ovarian follicle morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Gdf9-icre)5092Coo/?	involves: 129S4/SvJae * C57BL/6J	N	19843540
MGI:4941741	F	MP:0001131	abnormal ovarian follicle morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tsc1<tm1Djk>/Tsc1<tm1Djk>,Tg(Gdf9-icre)5092Coo/?	involves: 129S4/SvJae * C57BL/6J	N	19843540
MGI:4941742	M	MP:0004851	increased testis weight	Tbc1d4<tm1.1Arte>/Tbc1d4<tm1.1Arte>	involves: C57BL/6	N	21195350
MGI:4941744	F	MP:0001131	abnormal ovarian follicle morphology	Pdpk1<tm1Maka>/Pdpk1<tm1Maka>,Tsc1<tm1Djk>/Tsc1<tm1Djk>,Tg(Gdf9-icre)5092Coo/?	involves: 129S4/SvJae * C57BL/6J	N	19843540
MGI:4941746	F	MP:0008000	increased ovary tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ctnnb1<tm1Mmt>/Ctnnb1<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ	N	18687666
MGI:4941746	M	MP:0006262	increased testis tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ctnnb1<tm1Mmt>/Ctnnb1<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ	N	19237610
MGI:4941746	M	MP:0001154	seminiferous tubule degeneration	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ctnnb1<tm1Mmt>/Ctnnb1<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ	N	19237610
MGI:4941778	M	MP:0014365	impaired short-term object recognition memory	Slc6a8<tm1.2Clar>/Y	involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL	N	21249153
MGI:4941778	M	MP:0001402	decreased locomotor activity	Slc6a8<tm1.2Clar>/Y	involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL	N	21249153
MGI:4941778	M	MP:0010062	decreased creatine level	Slc6a8<tm1.2Clar>/Y	involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL	N	21249153
MGI:4941778	M	MP:0010065	decreased circulating creatine level	Slc6a8<tm1.2Clar>/Y	involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL	N	21249153
MGI:4941778	M	MP:0001399	hyperactivity	Slc6a8<tm1.2Clar>/Y	involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL	N	21249153
MGI:4941778	M	MP:0005386	behavior/neurological phenotype	Slc6a8<tm1.2Clar>/Y	involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL	Y	21249153
MGI:4941778	M	MP:0009454	impaired contextual conditioning behavior	Slc6a8<tm1.2Clar>/Y	involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL	N	21249153
MGI:4941778	M	MP:0001463	abnormal spatial learning	Slc6a8<tm1.2Clar>/Y	involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL	N	21249153
MGI:4941778	M	MP:0001262	decreased body weight	Slc6a8<tm1.2Clar>/Y	involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL	N	21249153
MGI:4941778	M	MP:0001522	impaired swimming	Slc6a8<tm1.2Clar>/Y	involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL	N	21249153
MGI:4941778	M	MP:0010069	increased serotonin level	Slc6a8<tm1.2Clar>/Y	involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL	N	21249153
MGI:4941805	F	MP:0009442	increased ovarian teratoma incidence	Dclre1a<tm1Rleg>/Dclre1a<tm1Rleg>	involves: 129S7/SvEvBrd	N	16260620
MGI:4941948	M	MP:0001925	male infertility	Vangl2<ska17>/Vangl2<ska17>	involves: 129S6/SvEvTac * C57BL/6J	N	21404367
MGI:4941948	F	MP:0003540	imperforate hymen	Vangl2<ska17>/Vangl2<ska17>	involves: 129S6/SvEvTac * C57BL/6J	N	21404367
MGI:4941978	F	MP:0001926	female infertility	Ooep<tm1Miya>/Ooep<tm1Miya>	involves: 129P2/OlaHsd * C57BL/6J	N	20590823
MGI:4942351	F	MP:0012411	increased granulosa cell tumor incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJae * 129S7/SvEvBrd	N	25815421
MGI:4942351	F	MP:0012411	increased granulosa cell tumor incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJae * 129S7/SvEvBrd	N	18687666
MGI:4942351	F	MP:0009661	abnormal pregnancy	Pten<tm1Hwu>/Pten<tm1Hwu>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJae * 129S7/SvEvBrd	N	18687666
MGI:4942412	M	MP:0004901	decreased male germ cell number	Itpa<tm1Skmi>/Itpa<tm1Skmi>	involves: 129S/SvEv * C57BL/6J	N	19498443
MGI:4943514	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Hspa5<tm1Alee>/Hspa5<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/?	involves: 129 * 129S4/SvJae * C57BL/6 * DBA/2	N	19033462
MGI:4943514	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Hspa5<tm1Alee>/Hspa5<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/?	involves: 129 * 129S4/SvJae * C57BL/6 * DBA/2	N	19033462
MGI:4943549	M	MP:0001155	arrest of spermatogenesis	Tdrd7<nmf166>/Tdrd7<nmf166>	involves: C3H * C57BL/6J	N	21436445
MGI:4943549	M	MP:0001925	male infertility	Tdrd7<nmf166>/Tdrd7<nmf166>	involves: C3H * C57BL/6J	N	21436445
MGI:4943575	F	MP:0005387	immune system phenotype	B9d2/Tgfb1<tm1Flv>/B9d2<+>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	Y	21435587
MGI:4943575	F	MP:0005378	growth/size/body region phenotype	B9d2/Tgfb1<tm1Flv>/B9d2<+>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	Y	21435587
MGI:4943575	F	MP:0004973	increased regulatory T cell number	B9d2/Tgfb1<tm1Flv>/B9d2<+>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	N	21435587
MGI:4943576	F	MP:0005378	growth/size/body region phenotype	B9d2/Tgfb1<tm1Flv>/Tgfb1<tm2Flv>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	Y	21435587
MGI:4943576	F	MP:0004973	increased regulatory T cell number	B9d2/Tgfb1<tm1Flv>/Tgfb1<tm2Flv>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	N	21435587
MGI:4943576	F	MP:0005387	immune system phenotype	B9d2/Tgfb1<tm1Flv>/Tgfb1<tm2Flv>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	Y	21435587
MGI:4943583	M	MP:0005169	abnormal male meiosis	Hsp90aa1<Gt(XE444)Byg>/Hsp90aa1<Gt(XE444)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21209834
MGI:4943583	M	MP:0004852	decreased testis weight	Hsp90aa1<Gt(XE444)Byg>/Hsp90aa1<Gt(XE444)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21209834
MGI:4943583	M	MP:0005159	azoospermia	Hsp90aa1<Gt(XE444)Byg>/Hsp90aa1<Gt(XE444)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21209834
MGI:4943583	M	MP:0008261	arrest of male meiosis	Hsp90aa1<Gt(XE444)Byg>/Hsp90aa1<Gt(XE444)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21209834
MGI:4943583	M	MP:0001925	male infertility	Hsp90aa1<Gt(XE444)Byg>/Hsp90aa1<Gt(XE444)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21209834
MGI:4943583	M	MP:0008280	abnormal male germ cell apoptosis	Hsp90aa1<Gt(XE444)Byg>/Hsp90aa1<Gt(XE444)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21209834
MGI:4943583	M	MP:0001147	small testis	Hsp90aa1<Gt(XE444)Byg>/Hsp90aa1<Gt(XE444)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21209834
MGI:4943584	M	MP:0001925	male infertility	Hsp90aa1<Gt(S17-2G1)Sor>/Hsp90aa1<Gt(S17-2G1)Sor>	involves: 129S4/SvJaeSor	N	21209834
MGI:4943702	F	MP:0002676	uterus hyperplasia	Errfi1<tm1Jwj>/Errfi1<tm1Jwj>,Gt(ROSA)26Sor<tm1(cre/ERT2)Thl>/Gt(ROSA)26Sor<+>	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	19710174
MGI:4943868	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm5(Myh7-GFP,Myh6-CFP)Unc>/Y	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J	N	18755891
MGI:4944272	F	MP:0004904	increased uterus weight	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	20418913
MGI:4944272	F	MP:0004904	increased uterus weight	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	25377472
MGI:4944272	F	MP:0009092	endometrium hyperplasia	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	20418913
MGI:4944272	F	MP:0004905	decreased uterus weight	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	25377472
MGI:4944272	F	MP:0004868	increased endometrial carcinoma incidence	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	20418913
MGI:4944272	F	MP:0002014	increased papilloma incidence	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	25377472
MGI:4944272	F	MP:0009671	abnormal uterus physiology	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	20418913
MGI:4944272	F	MP:0002083	premature death	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	25377472
MGI:4944272	F	MP:0004868	increased endometrial carcinoma incidence	Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	25377472
MGI:4944273	F	MP:0004896	abnormal endometrium morphology	Errfi1<tm1Jwj>/Errfi1<tm1Jwj>,Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	20418913
MGI:4944273	F	MP:0004904	increased uterus weight	Errfi1<tm1Jwj>/Errfi1<tm1Jwj>,Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	20418913
MGI:4944273	F	MP:0004868	increased endometrial carcinoma incidence	Errfi1<tm1Jwj>/Errfi1<tm1Jwj>,Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	20418913
MGI:4944273	F	MP:0009092	endometrium hyperplasia	Errfi1<tm1Jwj>/Errfi1<tm1Jwj>,Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	20418913
MGI:4946255	F	MP:0003822	decreased left ventricle systolic pressure	Maoa<tm1Shih>/Maoa<tm1Shih>	involves: 129S4/SvJae	N	19910579
MGI:4946255	F	MP:0004486	decreased response of heart to induced stress	Maoa<tm1Shih>/Maoa<tm1Shih>	involves: 129S4/SvJae	N	19910579
MGI:4946255	F	MP:0004215	abnormal myocardial fiber physiology	Maoa<tm1Shih>/Maoa<tm1Shih>	involves: 129S4/SvJae	N	19910579
MGI:4946295	M	MP:0001156	abnormal spermatogenesis	Trp53<tm1Brd>/Trp53<tm8Xu>	involves: 129S7/SvEvBrd	N	20818388
MGI:4946295	M	MP:0001147	small testis	Trp53<tm1Brd>/Trp53<tm8Xu>	involves: 129S7/SvEvBrd	N	20818388
MGI:4946295	M	MP:0008280	abnormal male germ cell apoptosis	Trp53<tm1Brd>/Trp53<tm8Xu>	involves: 129S7/SvEvBrd	N	20818388
MGI:4946386	F	MP:0013401	increased endometrial gland number	Wnt11<tm1.1Khay>/Wnt11<tm1.2Khay>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	20962251
MGI:4946386	F	MP:0009671	abnormal uterus physiology	Wnt11<tm1.1Khay>/Wnt11<tm1.2Khay>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	20962251
MGI:4946514	M	MP:0003698	abnormal male reproductive system physiology	Pld6<tm1.1Mafr>/Pld6<tm1.1Mafr>	involves: C57BL/6	N	21397848
MGI:4946514	M	MP:0002216	abnormal seminiferous tubule morphology	Pld6<tm1.1Mafr>/Pld6<tm1.1Mafr>	involves: C57BL/6	N	21397848
MGI:4946514	M	MP:0001925	male infertility	Pld6<tm1.1Mafr>/Pld6<tm1.1Mafr>	involves: C57BL/6	N	21397848
MGI:4946514	M	MP:0006379	abnormal spermatocyte morphology	Pld6<tm1.1Mafr>/Pld6<tm1.1Mafr>	involves: C57BL/6	N	21397848
MGI:4946514	M	MP:0008261	arrest of male meiosis	Pld6<tm1.1Mafr>/Pld6<tm1.1Mafr>	involves: C57BL/6	N	21397848
MGI:4946515	M	MP:0006379	abnormal spermatocyte morphology	Lpin1<fld>/Lpin1<fld>	involves: BALB/cByJ	N	21397848
MGI:4946609	M	MP:0005159	azoospermia	Ranbp1<tm1Yyo>/Ranbp1<tm1Yyo>	involves: 129S2/SvPas * C57BL/6	N	21310149
MGI:4946609	M	MP:0008280	abnormal male germ cell apoptosis	Ranbp1<tm1Yyo>/Ranbp1<tm1Yyo>	involves: 129S2/SvPas * C57BL/6	N	21310149
MGI:4946609	M	MP:0001156	abnormal spermatogenesis	Ranbp1<tm1Yyo>/Ranbp1<tm1Yyo>	involves: 129S2/SvPas * C57BL/6	N	21310149
MGI:4946609	M	MP:0001925	male infertility	Ranbp1<tm1Yyo>/Ranbp1<tm1Yyo>	involves: 129S2/SvPas * C57BL/6	N	21310149
MGI:4946639	M	MP:0006379	abnormal spermatocyte morphology	Tdrd5<tm1Sait>/Tdrd5<tm1Sait>	involves: C57BL/6 * CBA	N	21383078
MGI:4946639	M	MP:0002686	globozoospermia	Tdrd5<tm1Sait>/Tdrd5<tm1Sait>	involves: C57BL/6 * CBA	N	21383078
MGI:4946639	M	MP:0001153	small seminiferous tubules	Tdrd5<tm1Sait>/Tdrd5<tm1Sait>	involves: C57BL/6 * CBA	N	21383078
MGI:4946639	M	MP:0008280	abnormal male germ cell apoptosis	Tdrd5<tm1Sait>/Tdrd5<tm1Sait>	involves: C57BL/6 * CBA	N	21383078
MGI:4946639	M	MP:0008898	abnormal acrosome morphology	Tdrd5<tm1Sait>/Tdrd5<tm1Sait>	involves: C57BL/6 * CBA	N	21383078
MGI:4946639	M	MP:0001147	small testis	Tdrd5<tm1Sait>/Tdrd5<tm1Sait>	involves: C57BL/6 * CBA	N	21383078
MGI:4946639	M	MP:0001925	male infertility	Tdrd5<tm1Sait>/Tdrd5<tm1Sait>	involves: C57BL/6 * CBA	N	21383078
MGI:4946639	M	MP:0008261	arrest of male meiosis	Tdrd5<tm1Sait>/Tdrd5<tm1Sait>	involves: C57BL/6 * CBA	N	21383078
MGI:4946639	M	MP:0001155	arrest of spermatogenesis	Tdrd5<tm1Sait>/Tdrd5<tm1Sait>	involves: C57BL/6 * CBA	N	21383078
MGI:4946639	M	MP:0004852	decreased testis weight	Tdrd5<tm1Sait>/Tdrd5<tm1Sait>	involves: C57BL/6 * CBA	N	21383078
MGI:4946828	M	MP:0002774	small prostate gland	Ar<tm3.1(AR)Ska>/Y	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946828	M	MP:0001921	reduced fertility	Ar<tm3.1(AR)Ska>/Y	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946828	M	MP:0002781	increased circulating testosterone level	Ar<tm3.1(AR)Ska>/Y	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946828	M	MP:0001153	small seminiferous tubules	Ar<tm3.1(AR)Ska>/Y	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946828	M	MP:0004962	decreased prostate gland weight	Ar<tm3.1(AR)Ska>/Y	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946829	M	MP:0001921	reduced fertility	Ar<tm3.1(AR)Ska>/Y,Tg(KLKB1-cre/ERT2)1Pcn/0	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946829	M	MP:0004961	increased prostate gland weight	Ar<tm3.1(AR)Ska>/Y,Tg(KLKB1-cre/ERT2)1Pcn/0	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946829	M	MP:0002781	increased circulating testosterone level	Ar<tm3.1(AR)Ska>/Y,Tg(KLKB1-cre/ERT2)1Pcn/0	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946829	M	MP:0031364	increased prostate gland ventral lobe weight	Ar<tm3.1(AR)Ska>/Y,Tg(KLKB1-cre/ERT2)1Pcn/0	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946829	M	MP:0003607	abnormal prostate gland physiology	Ar<tm3.1(AR)Ska>/Y,Tg(KLKB1-cre/ERT2)1Pcn/0	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946830	M	MP:0010357	increased prostate gland tumor incidence	Ar<tm3.1(AR)Ska>/Y,Tg(KLKB1-cre/ERT2)1Pcn/0,Tg(TRAMP)8247Ng/0	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946830	M	MP:0003448	abnormal tumor morphology	Ar<tm3.1(AR)Ska>/Y,Tg(KLKB1-cre/ERT2)1Pcn/0,Tg(TRAMP)8247Ng/0	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946830	M	MP:0010308	decreased tumor latency	Ar<tm3.1(AR)Ska>/Y,Tg(KLKB1-cre/ERT2)1Pcn/0,Tg(TRAMP)8247Ng/0	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946830	M	MP:0002083	premature death	Ar<tm3.1(AR)Ska>/Y,Tg(KLKB1-cre/ERT2)1Pcn/0,Tg(TRAMP)8247Ng/0	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946830	M	MP:0003721	increased tumor growth/size	Ar<tm3.1(AR)Ska>/Y,Tg(KLKB1-cre/ERT2)1Pcn/0,Tg(TRAMP)8247Ng/0	involves: C57BL/6 * C57BL/6J * CBA	N	21383160
MGI:4946933	M	MP:0008261	arrest of male meiosis	Pld6<tm1.1Hsas>/Pld6<tm1.1Hsas>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21397847
MGI:4946933	M	MP:0006380	abnormal spermatid morphology	Pld6<tm1.1Hsas>/Pld6<tm1.1Hsas>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21397847
MGI:4946933	M	MP:0001147	small testis	Pld6<tm1.1Hsas>/Pld6<tm1.1Hsas>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21397847
MGI:4946933	M	MP:0004884	abnormal testis physiology	Pld6<tm1.1Hsas>/Pld6<tm1.1Hsas>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21397847
MGI:4946933	M	MP:0006362	abnormal male germ cell morphology	Pld6<tm1.1Hsas>/Pld6<tm1.1Hsas>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21397847
MGI:4946933	M	MP:0008280	abnormal male germ cell apoptosis	Pld6<tm1.1Hsas>/Pld6<tm1.1Hsas>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21397847
MGI:4946933	M	MP:0006379	abnormal spermatocyte morphology	Pld6<tm1.1Hsas>/Pld6<tm1.1Hsas>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21397847
MGI:4946933	M	MP:0005159	azoospermia	Pld6<tm1.1Hsas>/Pld6<tm1.1Hsas>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21397847
MGI:4946933	M	MP:0001925	male infertility	Pld6<tm1.1Hsas>/Pld6<tm1.1Hsas>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21397847
MGI:4946943	F	MP:0005389	reproductive system phenotype	Calr3<tm1Osb>/Calr3<tm1Osb>	involves: 129S2/SvPas * C57BL/6	Y	21131354
MGI:4946943	M	MP:0001925	male infertility	Calr3<tm1Osb>/Calr3<tm1Osb>	involves: 129S2/SvPas * C57BL/6	N	21131354
MGI:4946943	M	MP:0030978	impaired binding of sperm to zona pellucida	Calr3<tm1Osb>/Calr3<tm1Osb>	involves: 129S2/SvPas * C57BL/6	N	21131354
MGI:4946943	M	MP:0031012	impaired sperm migration in female genital tract	Calr3<tm1Osb>/Calr3<tm1Osb>	involves: 129S2/SvPas * C57BL/6	N	21131354
MGI:4946943	M	MP:0000242	impaired fertilization	Calr3<tm1Osb>/Calr3<tm1Osb>	involves: 129S2/SvPas * C57BL/6	N	21131354
MGI:4947225	M	MP:0001925	male infertility	Derl2<tm1.2Hpl>/Derl2<tm1.2Hpl>	involves: BALB/cJ	N	21220515
MGI:4947226	M	MP:0002687	oligozoospermia	Del(2Cd59b-Cd59a)1Jha/Del(2Cd59b-Cd59a)1Jha	B6.129-Del(2Cd59b-Cd59a)1Jha	N	19051264
MGI:4947226	M	MP:0001922	reduced male fertility	Del(2Cd59b-Cd59a)1Jha/Del(2Cd59b-Cd59a)1Jha	B6.129-Del(2Cd59b-Cd59a)1Jha	N	19051264
MGI:4947283	F	MP:0001926	female infertility	Ptpn6<me-B2>/Ptpn6<me-B2>	involves: BALB/c	N	21435452
MGI:4947283	F	MP:0011130	absent tertiary ovarian follicles	Ptpn6<me-B2>/Ptpn6<me-B2>	involves: BALB/c	N	21435452
MGI:4947283	F	MP:0004833	ovary atrophy	Ptpn6<me-B2>/Ptpn6<me-B2>	involves: BALB/c	N	21435452
MGI:4947941	F	MP:0001212	skin lesions	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947941	F	MP:0001805	decreased IgG level	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947941	F	MP:0001661	extended life span	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947941	F	MP:0002460	decreased immunoglobulin level	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947941	F	MP:0003726	decreased autoantibody level	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947941	F	MP:0000414	alopecia	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947941	F	MP:0002135	abnormal kidney morphology	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947942	M	MP:0001661	extended life span	Cd40lg<tm1Flv>/Y,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947942	M	MP:0002460	decreased immunoglobulin level	Cd40lg<tm1Flv>/Y,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947942	M	MP:0003726	decreased autoantibody level	Cd40lg<tm1Flv>/Y,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947942	M	MP:0000414	alopecia	Cd40lg<tm1Flv>/Y,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947942	M	MP:0001805	decreased IgG level	Cd40lg<tm1Flv>/Y,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947942	M	MP:0001212	skin lesions	Cd40lg<tm1Flv>/Y,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947942	M	MP:0002135	abnormal kidney morphology	Cd40lg<tm1Flv>/Y,Fas<lpr>/Fas<lpr>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947943	M	MP:0003726	decreased autoantibody level	Cd40lg<tm1Flv>/Y,Fas<lpr>/Fas<lpr>,Tcra<tm1Mjo>/Tcra<tm1Mjo>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947943	M	MP:0004762	increased anti-double stranded DNA antibody level	Cd40lg<tm1Flv>/Y,Fas<lpr>/Fas<lpr>,Tcra<tm1Mjo>/Tcra<tm1Mjo>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947943	M	MP:0002135	abnormal kidney morphology	Cd40lg<tm1Flv>/Y,Fas<lpr>/Fas<lpr>,Tcra<tm1Mjo>/Tcra<tm1Mjo>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947943	M	MP:0010771	integument phenotype	Cd40lg<tm1Flv>/Y,Fas<lpr>/Fas<lpr>,Tcra<tm1Mjo>/Tcra<tm1Mjo>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	Y	9036998
MGI:4947944	F	MP:0002135	abnormal kidney morphology	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>,Fas<lpr>/Fas<lpr>,Tcra<tm1Mjo>/Tcra<tm1Mjo>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947944	F	MP:0010771	integument phenotype	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>,Fas<lpr>/Fas<lpr>,Tcra<tm1Mjo>/Tcra<tm1Mjo>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	Y	9036998
MGI:4947944	F	MP:0004762	increased anti-double stranded DNA antibody level	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>,Fas<lpr>/Fas<lpr>,Tcra<tm1Mjo>/Tcra<tm1Mjo>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4947944	F	MP:0003726	decreased autoantibody level	Cd40lg<tm1Flv>/Cd40lg<tm1Flv>,Fas<lpr>/Fas<lpr>,Tcra<tm1Mjo>/Tcra<tm1Mjo>	involves: 129P2/OlaHsd * 129S2/SvPas * MRL	N	9036998
MGI:4948089	M	MP:0002687	oligozoospermia	Trim28<tm1.1Ipc>/Trim28<tm1.1Ipc>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21163256
MGI:4948089	M	MP:0004901	decreased male germ cell number	Trim28<tm1.1Ipc>/Trim28<tm1.1Ipc>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21163256
MGI:4948089	M	MP:0013600	testis degeneration	Trim28<tm1.1Ipc>/Trim28<tm1.1Ipc>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21163256
MGI:4948089	M	MP:0006380	abnormal spermatid morphology	Trim28<tm1.1Ipc>/Trim28<tm1.1Ipc>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21163256
MGI:4948089	M	MP:0004852	decreased testis weight	Trim28<tm1.1Ipc>/Trim28<tm1.1Ipc>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21163256
MGI:4948089	M	MP:0001922	reduced male fertility	Trim28<tm1.1Ipc>/Trim28<tm1.1Ipc>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21163256
MGI:4948089	M	MP:0004182	abnormal spermiation	Trim28<tm1.1Ipc>/Trim28<tm1.1Ipc>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21163256
MGI:4948267	M	MP:0001146	abnormal testis morphology	Rpl31<Dts>/Rpl31<+>	CBA/J-Rpl31<Dts>/GrsrJ	N	MGI:4948255
MGI:4948269	F	MP:0001923	reduced female fertility	Cdc14b<tm1.2Pzg>/Cdc14b<tm1.2Pzg>	B6.129P2-Cdc14b<tm1.2Pzg>	N	21262768
MGI:4948269	M	MP:0001922	reduced male fertility	Cdc14b<tm1.2Pzg>/Cdc14b<tm1.2Pzg>	B6.129P2-Cdc14b<tm1.2Pzg>	N	21262768
MGI:4948588	F	MP:0002577	reduced enamel thickness	Amelx<tm3Msnd>/Amelx<tm3Msnd>	involves: 129X1/SvJ * C57BL/6	N	MGI:4944210
MGI:4948967	F	MP:0000630	mammary gland hyperplasia	Map2k7<tm1.1Twad>/Map2k7<tm1.2Twad>,Tg(MMTV-cre)4Mam/0,Tg(MMTV-Erbb2)1Pv/0	involves: 129P2/OlaHsd * C57BL/6 * CD-1 * DBA * FVB/N	N	21317887
MGI:4949144	M	MP:0002687	oligozoospermia	Bglap/Bglap2<tm3.1Kry>/Bglap/Bglap2<tm3.1Kry>,Tg(Col1a1-cre)1Kry/0	involves: FVB	N	21333348
MGI:4949144	M	MP:0001147	small testis	Bglap/Bglap2<tm3.1Kry>/Bglap/Bglap2<tm3.1Kry>,Tg(Col1a1-cre)1Kry/0	involves: FVB	N	21333348
MGI:4949144	M	MP:0004910	decreased seminal vesicle weight	Bglap/Bglap2<tm3.1Kry>/Bglap/Bglap2<tm3.1Kry>,Tg(Col1a1-cre)1Kry/0	involves: FVB	N	21333348
MGI:4949144	M	MP:0004852	decreased testis weight	Bglap/Bglap2<tm3.1Kry>/Bglap/Bglap2<tm3.1Kry>,Tg(Col1a1-cre)1Kry/0	involves: FVB	N	21333348
MGI:4949144	M	MP:0004929	decreased epididymis weight	Bglap/Bglap2<tm3.1Kry>/Bglap/Bglap2<tm3.1Kry>,Tg(Col1a1-cre)1Kry/0	involves: FVB	N	21333348
MGI:4949147	M	MP:0001147	small testis	Bglap/Bglap2<tm3.1Kry>/Bglap/Bglap2<tm3.1Kry>,Tg(Col1a1-cre)1Kry/0	involves: FVB	N	21333348
MGI:4949147	M	MP:0004910	decreased seminal vesicle weight	Bglap/Bglap2<tm3.1Kry>/Bglap/Bglap2<tm3.1Kry>,Tg(Col1a1-cre)1Kry/0	involves: FVB	N	21333348
MGI:4949147	M	MP:0004852	decreased testis weight	Bglap/Bglap2<tm3.1Kry>/Bglap/Bglap2<tm3.1Kry>,Tg(Col1a1-cre)1Kry/0	involves: FVB	N	21333348
MGI:4949147	M	MP:0004929	decreased epididymis weight	Bglap/Bglap2<tm3.1Kry>/Bglap/Bglap2<tm3.1Kry>,Tg(Col1a1-cre)1Kry/0	involves: FVB	N	21333348
MGI:4949147	M	MP:0002687	oligozoospermia	Bglap/Bglap2<tm3.1Kry>/Bglap/Bglap2<tm3.1Kry>,Tg(Col1a1-cre)1Kry/0	involves: FVB	N	21333348
MGI:4949150	M	MP:0002687	oligozoospermia	Gprc6a<tm1.1Kry>/Gprc6a<tm1.1Kry>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949150	M	MP:0004910	decreased seminal vesicle weight	Gprc6a<tm1.1Kry>/Gprc6a<tm1.1Kry>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949150	M	MP:0004852	decreased testis weight	Gprc6a<tm1.1Kry>/Gprc6a<tm1.1Kry>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949150	M	MP:0004929	decreased epididymis weight	Gprc6a<tm1.1Kry>/Gprc6a<tm1.1Kry>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949150	M	MP:0001147	small testis	Gprc6a<tm1.1Kry>/Gprc6a<tm1.1Kry>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949150	M	MP:0014052	increased male germ cell apoptosis	Gprc6a<tm1.1Kry>/Gprc6a<tm1.1Kry>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949151	M	MP:0004852	decreased testis weight	Bglap/Bglap2<tm3.1Kry>/Bglap<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949151	M	MP:0004910	decreased seminal vesicle weight	Bglap/Bglap2<tm3.1Kry>/Bglap<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949151	M	MP:0002687	oligozoospermia	Bglap/Bglap2<tm3.1Kry>/Bglap<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949151	M	MP:0004929	decreased epididymis weight	Bglap/Bglap2<tm3.1Kry>/Bglap<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949151	M	MP:0001147	small testis	Bglap/Bglap2<tm3.1Kry>/Bglap<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949152	M	MP:0001147	small testis	Bglap/Bglap2<tm3.1Kry>/Bglap2<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949152	M	MP:0004910	decreased seminal vesicle weight	Bglap/Bglap2<tm3.1Kry>/Bglap2<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949152	M	MP:0004852	decreased testis weight	Bglap/Bglap2<tm3.1Kry>/Bglap2<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949152	M	MP:0002687	oligozoospermia	Bglap/Bglap2<tm3.1Kry>/Bglap2<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949152	M	MP:0004929	decreased epididymis weight	Bglap/Bglap2<tm3.1Kry>/Bglap2<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: C57BL/6J	N	21333348
MGI:4949155	M	MP:0001147	small testis	Creb1<tm3Gsc>/Creb1<tm3Gsc>,Tg(Cyp17a1-icre)AJako/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	21333348
MGI:4949155	M	MP:0004852	decreased testis weight	Creb1<tm3Gsc>/Creb1<tm3Gsc>,Tg(Cyp17a1-icre)AJako/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	21333348
MGI:4949155	M	MP:0004929	decreased epididymis weight	Creb1<tm3Gsc>/Creb1<tm3Gsc>,Tg(Cyp17a1-icre)AJako/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	21333348
MGI:4949155	M	MP:0004910	decreased seminal vesicle weight	Creb1<tm3Gsc>/Creb1<tm3Gsc>,Tg(Cyp17a1-icre)AJako/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	21333348
MGI:4949155	M	MP:0002687	oligozoospermia	Creb1<tm3Gsc>/Creb1<tm3Gsc>,Tg(Cyp17a1-icre)AJako/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	21333348
MGI:4949156	M	MP:0004929	decreased epididymis weight	Creb1<tm3Gsc>/Creb1<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	21333348
MGI:4949156	M	MP:0004910	decreased seminal vesicle weight	Creb1<tm3Gsc>/Creb1<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	21333348
MGI:4949156	M	MP:0001147	small testis	Creb1<tm3Gsc>/Creb1<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	21333348
MGI:4949156	M	MP:0002687	oligozoospermia	Creb1<tm3Gsc>/Creb1<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	21333348
MGI:4949156	M	MP:0004852	decreased testis weight	Creb1<tm3Gsc>/Creb1<+>,Gprc6a<tm1.1Kry>/Gprc6a<+>,Tg(Cyp17a1-icre)AJako/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	21333348
MGI:4949205	F	MP:0004832	enlarged ovary	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0009442	increased ovarian teratoma incidence	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0002777	absent ovarian follicles	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0001134	absent corpus luteum	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0001131	abnormal ovarian follicle morphology	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0003507	abnormal ovary physiology	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0012736	abnormal polar body morphology	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0011121	decreased primordial ovarian follicle number	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0002681	increased corpora lutea number	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0008871	abnormal ovarian follicle number	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0031383	increased secondary ovarian follicle number	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0001125	abnormal oocyte morphology	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0009648	abnormal superovulation	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0011125	decreased primary ovarian follicle number	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0009361	abnormal primordial ovarian follicle morphology	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949205	F	MP:0001931	abnormal oogenesis	Foxo3<mommeR1>/Foxo3<mommeR1>,Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew	FVB/NJ-Foxo3<mommeR1> Tg(HBA1-Gfp)1Ew	N	21347845
MGI:4949206	F	MP:0011125	decreased primary ovarian follicle number	Foxo3<mommeR1>/Foxo3<tm1.1Rdp>,Tg(HBA1-GFP)1Ew/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ	N	21347845
MGI:4949206	F	MP:0011121	decreased primordial ovarian follicle number	Foxo3<mommeR1>/Foxo3<tm1.1Rdp>,Tg(HBA1-GFP)1Ew/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ	N	21347845
MGI:4949206	F	MP:0002777	absent ovarian follicles	Foxo3<mommeR1>/Foxo3<tm1.1Rdp>,Tg(HBA1-GFP)1Ew/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ	N	21347845
MGI:4949233	M	MP:0001934	increased litter size	Rbm44<tm1.1Zuk>/Rbm44<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	21364893
MGI:4949233	M	MP:0031425	enhanced male fertility	Rbm44<tm1.1Zuk>/Rbm44<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	21364893
MGI:4949233	M	MP:0030603	increased sperm number	Rbm44<tm1.1Zuk>/Rbm44<tm1.1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	21364893
MGI:4949234	M	MP:0031425	enhanced male fertility	Rbm44<tm1.1Zuk>/Rbm44<+>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	21364893
MGI:4949234	M	MP:0030603	increased sperm number	Rbm44<tm1.1Zuk>/Rbm44<+>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	21364893
MGI:4949234	M	MP:0001934	increased litter size	Rbm44<tm1.1Zuk>/Rbm44<+>	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	21364893
MGI:4949269	M	MP:0001925	male infertility	Mir9-3<tm1Sia>/Mir9-3<tm1Sia>	involves: C57BL/6 * CBA	N	21368052
MGI:4949269	F	MP:0001926	female infertility	Mir9-3<tm1Sia>/Mir9-3<tm1Sia>	involves: C57BL/6 * CBA	N	21368052
MGI:4949470	F	MP:0009047	short metestrus	Gnrh1<tm1.1Hjn>/Gnrh1<tm1.1Hjn>	involves: C57BL/6	N	21368045
MGI:4949470	F	MP:0009012	short diestrus	Gnrh1<tm1.1Hjn>/Gnrh1<tm1.1Hjn>	involves: C57BL/6	N	21368045
MGI:4949470	F	MP:0003699	abnormal female reproductive system physiology	Gnrh1<tm1.1Hjn>/Gnrh1<tm1.1Hjn>	involves: C57BL/6	N	21368045
MGI:4949470	F	MP:0003507	abnormal ovary physiology	Gnrh1<tm1.1Hjn>/Gnrh1<tm1.1Hjn>	involves: C57BL/6	N	21368045
MGI:4949470	F	MP:0009007	short estrous cycle	Gnrh1<tm1.1Hjn>/Gnrh1<tm1.1Hjn>	involves: C57BL/6	N	21368045
MGI:4949470	F	MP:0009015	short proestrus	Gnrh1<tm1.1Hjn>/Gnrh1<tm1.1Hjn>	involves: C57BL/6	N	21368045
MGI:4949537	M	MP:0001925	male infertility	Agps<bs2>/Agps<bs2>	STOCK Agps<bs2>/J	N	16332269
MGI:4949537	M	MP:0002216	abnormal seminiferous tubule morphology	Agps<bs2>/Agps<bs2>	STOCK Agps<bs2>/J	N	21353609
MGI:4949537	M	MP:0001147	small testis	Agps<bs2>/Agps<bs2>	STOCK Agps<bs2>/J	N	21353609
MGI:4949537	M	MP:0001925	male infertility	Agps<bs2>/Agps<bs2>	STOCK Agps<bs2>/J	N	21353609
MGI:4949537	M	MP:0005159	azoospermia	Agps<bs2>/Agps<bs2>	STOCK Agps<bs2>/J	N	21353609
MGI:4949538	M	MP:0005578	teratozoospermia	Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>	FVB/NTac-Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Mmmh	N	20034429
MGI:4949538	M	MP:0008898	abnormal acrosome morphology	Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>	FVB/NTac-Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Mmmh	N	20034429
MGI:4949538	M	MP:0001925	male infertility	Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>	FVB/NTac-Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Mmmh	N	20034429
MGI:4949538	M	MP:0004901	decreased male germ cell number	Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>	FVB/NTac-Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Mmmh	N	20034429
MGI:4949538	M	MP:0005159	azoospermia	Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>	FVB/NTac-Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Mmmh	N	20034429
MGI:4949538	M	MP:0009831	abnormal sperm midpiece morphology	Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>	FVB/NTac-Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Mmmh	N	20034429
MGI:4949538	M	MP:0001154	seminiferous tubule degeneration	Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>	FVB/NTac-Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Mmmh	N	20034429
MGI:4949538	M	MP:0002675	asthenozoospermia	Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>	FVB/NTac-Nup210l<Tg(Gt(ROSA)26Sor-EGFP)130910Eps>/Mmmh	N	20034429
MGI:4949667	F	MP:0008537	increased susceptibility to induced colitis	Tktl1<tm1Arte>/Tktl1<tm1Arte>	C57BL/6-Tktl1<tm1Arte>	N	21233279
MGI:4949667	F	MP:0010180	increased susceptibility to weight loss	Tktl1<tm1Arte>/Tktl1<tm1Arte>	C57BL/6-Tktl1<tm1Arte>	N	21233279
MGI:4949839	M	MP:0004543	abnormal sperm physiology	Kcnu1<tm1.1Clin>/Kcnu1<tm1.1Clin>	involves: C57BL/6 * C57BL/6NTac * SJL	N	21427226
MGI:4949840	M	MP:0000242	impaired fertilization	Kcnu1<tm1.2Clin>/Kcnu1<tm1.2Clin>	B6.Cg-Kcnu1<tm1.2Clin>	N	21427226
MGI:4949840	M	MP:0001925	male infertility	Kcnu1<tm1.2Clin>/Kcnu1<tm1.2Clin>	B6.Cg-Kcnu1<tm1.2Clin>	N	21427226
MGI:4949840	M	MP:0004543	abnormal sperm physiology	Kcnu1<tm1.2Clin>/Kcnu1<tm1.2Clin>	B6.Cg-Kcnu1<tm1.2Clin>	N	21427226
MGI:4949840	M	MP:0002675	asthenozoospermia	Kcnu1<tm1.2Clin>/Kcnu1<tm1.2Clin>	B6.Cg-Kcnu1<tm1.2Clin>	N	21427226
MGI:4949841	M	MP:0004543	abnormal sperm physiology	Kcnu1<tm1.2Clin>/Kcnu1<+>	B6.Cg-Kcnu1<tm1.2Clin>	N	21427226
MGI:4949887	F	MP:0010768	mortality/aging	Mecp2<tm1Vnar>/Mecp2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	Y	20163734
MGI:4949887	F	MP:0005386	behavior/neurological phenotype	Mecp2<tm1Vnar>/Mecp2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	Y	20163734
MGI:4949887	F	MP:0005389	reproductive system phenotype	Mecp2<tm1Vnar>/Mecp2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	Y	20163734
MGI:4949888	M	MP:0000886	abnormal cerebellar granule layer morphology	Mecp2<tm1Vnar>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	N	20163734
MGI:4949888	M	MP:0010768	mortality/aging	Mecp2<tm1Vnar>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	Y	20163734
MGI:4949888	M	MP:0000807	abnormal hippocampus morphology	Mecp2<tm1Vnar>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	N	20163734
MGI:4949888	M	MP:0005386	behavior/neurological phenotype	Mecp2<tm1Vnar>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	Y	20163734
MGI:4949888	M	MP:0005378	growth/size/body region phenotype	Mecp2<tm1Vnar>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	Y	20163734
MGI:4949888	M	MP:0000812	abnormal dentate gyrus morphology	Mecp2<tm1Vnar>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	N	20163734
MGI:4949888	M	MP:0000819	abnormal olfactory bulb morphology	Mecp2<tm1Vnar>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	N	20163734
MGI:4949888	M	MP:0008143	abnormal dendrite morphology	Mecp2<tm1Vnar>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	N	20163734
MGI:4949888	M	MP:0001925	male infertility	Mecp2<tm1Vnar>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	N	20163734
MGI:4949888	M	MP:0000849	abnormal cerebellum morphology	Mecp2<tm1Vnar>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	N	20163734
MGI:4949888	M	MP:0004170	abnormal orbitofrontal cortex morphology	Mecp2<tm1Vnar>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	N	20163734
MGI:4950025	F	MP:0001399	hyperactivity	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>,Rgs4<tm1Dgen>/Rgs4<tm1Dgen>	B6.129P2-Rgs4<tm1Dgen> Fmr1<tm1Cgr>	N	21215802
MGI:4950025	F	MP:0005386	behavior/neurological phenotype	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>,Rgs4<tm1Dgen>/Rgs4<tm1Dgen>	B6.129P2-Rgs4<tm1Dgen> Fmr1<tm1Cgr>	Y	21215802
MGI:4950025	F	MP:0001458	abnormal object recognition memory	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>,Rgs4<tm1Dgen>/Rgs4<tm1Dgen>	B6.129P2-Rgs4<tm1Dgen> Fmr1<tm1Cgr>	N	21215802
MGI:4950025	M	MP:0004851	increased testis weight	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>,Rgs4<tm1Dgen>/Rgs4<tm1Dgen>	B6.129P2-Rgs4<tm1Dgen> Fmr1<tm1Cgr>	N	21215802
MGI:4950025	F	MP:0002574	increased vertical activity	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>,Rgs4<tm1Dgen>/Rgs4<tm1Dgen>	B6.129P2-Rgs4<tm1Dgen> Fmr1<tm1Cgr>	N	21215802
MGI:4950025	F	MP:0005378	growth/size/body region phenotype	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>,Rgs4<tm1Dgen>/Rgs4<tm1Dgen>	B6.129P2-Rgs4<tm1Dgen> Fmr1<tm1Cgr>	Y	21215802
MGI:4950026	F	MP:0001458	abnormal object recognition memory	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	B6.129P2-Fmr1<tm1Cgr>	N	21215802
MGI:4950026	F	MP:0009712	impaired conditioned place preference behavior	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	B6.129P2-Fmr1<tm1Cgr>	N	21215802
MGI:4950026	F	MP:0001399	hyperactivity	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	B6.129P2-Fmr1<tm1Cgr>	N	21215802
MGI:4950026	F	MP:0001260	increased body weight	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	B6.129P2-Fmr1<tm1Cgr>	N	21215802
MGI:4950026	F	MP:0005386	behavior/neurological phenotype	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	B6.129P2-Fmr1<tm1Cgr>	Y	11008180
MGI:4950026	F	MP:0003863	decreased aggression towards mice	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	B6.129P2-Fmr1<tm1Cgr>	N	21215802
MGI:4950026	F	MP:0002574	increased vertical activity	Fmr1<tm1Cgr>/Fmr1<tm1Cgr>	B6.129P2-Fmr1<tm1Cgr>	N	21215802
MGI:4950027	M	MP:0009239	short sperm flagellum	Dpcd/Poll<Gt(OST280355)Lex>/Dpcd/Poll<Gt(OST280355)Lex>	involves: 129S5/SvEvBrd * C57BL/6Brd	N	20080492
MGI:4950027	M	MP:0001925	male infertility	Dpcd/Poll<Gt(OST280355)Lex>/Dpcd/Poll<Gt(OST280355)Lex>	involves: 129S5/SvEvBrd * C57BL/6Brd	N	20080492
MGI:4950027	M	MP:0002675	asthenozoospermia	Dpcd/Poll<Gt(OST280355)Lex>/Dpcd/Poll<Gt(OST280355)Lex>	involves: 129S5/SvEvBrd * C57BL/6Brd	N	21746835
MGI:4950027	M	MP:0005578	teratozoospermia	Dpcd/Poll<Gt(OST280355)Lex>/Dpcd/Poll<Gt(OST280355)Lex>	involves: 129S5/SvEvBrd * C57BL/6Brd	N	20080492
MGI:4950027	M	MP:0002675	asthenozoospermia	Dpcd/Poll<Gt(OST280355)Lex>/Dpcd/Poll<Gt(OST280355)Lex>	involves: 129S5/SvEvBrd * C57BL/6Brd	N	20080492
MGI:4950027	M	MP:0002686	globozoospermia	Dpcd/Poll<Gt(OST280355)Lex>/Dpcd/Poll<Gt(OST280355)Lex>	involves: 129S5/SvEvBrd * C57BL/6Brd	N	21746835
MGI:4950027	M	MP:0009239	short sperm flagellum	Dpcd/Poll<Gt(OST280355)Lex>/Dpcd/Poll<Gt(OST280355)Lex>	involves: 129S5/SvEvBrd * C57BL/6Brd	N	21746835
MGI:4950027	M	MP:0002686	globozoospermia	Dpcd/Poll<Gt(OST280355)Lex>/Dpcd/Poll<Gt(OST280355)Lex>	involves: 129S5/SvEvBrd * C57BL/6Brd	N	20080492
MGI:4950027	M	MP:0001925	male infertility	Dpcd/Poll<Gt(OST280355)Lex>/Dpcd/Poll<Gt(OST280355)Lex>	involves: 129S5/SvEvBrd * C57BL/6Brd	N	21746835
MGI:4950039	M	MP:0002687	oligozoospermia	Kdm2b<tm1Nobu>/Kdm2b<tm1Nobu>	either: (involves: 129S/SvEv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6J)	N	21220025
MGI:4950056	F	MP:0002495	increased IgA level	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0008181	increased marginal zone B cell number	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0008481	increased spleen germinal center number	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0012762	abnormal alpha-beta T cell morphology	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0002490	abnormal immunoglobulin level	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0008502	increased IgG3 level	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0008524	increased plasmacytoid dendritic cell number	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0005425	increased macrophage cell number	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0020519	renal glomerular immunoglobulin deposits	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0008501	increased IgG2b level	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0004794	increased anti-nuclear antigen antibody level	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0008097	increased plasma cell number	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0010768	mortality/aging	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	Y	30679154
MGI:4950056	F	MP:0002497	increased IgE level	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0002493	increased IgG level	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950056	F	MP:0002494	increased IgM level	Pld4<thss>/Pld4<thss>	BALB/cJ-Pld4<thss>/GrsrJ	N	30679154
MGI:4950062	M	MP:0004542	impaired acrosome reaction	Crisp4<tm1.2Mkob>/Crisp4<tm1.2Mkob>	involves: C57BL/6	N	21482758
MGI:4950069	M	MP:0009243	hairpin sperm flagellum	Ido1<tm1Alm>/Ido1<tm1Alm>	involves: 129X1/SvJ * BALB/c	N	21189261
MGI:4950069	M	MP:0030603	increased sperm number	Ido1<tm1Alm>/Ido1<tm1Alm>	involves: 129X1/SvJ * BALB/c	N	21189261
MGI:4950069	M	MP:0009236	pinhead sperm	Ido1<tm1Alm>/Ido1<tm1Alm>	involves: 129X1/SvJ * BALB/c	N	21189261
MGI:4950069	M	MP:0005578	teratozoospermia	Ido1<tm1Alm>/Ido1<tm1Alm>	involves: 129X1/SvJ * BALB/c	N	21189261
MGI:4950069	M	MP:0009233	enlarged sperm head	Ido1<tm1Alm>/Ido1<tm1Alm>	involves: 129X1/SvJ * BALB/c	N	21189261
MGI:4950069	M	MP:0002660	abnormal caput epididymis morphology	Ido1<tm1Alm>/Ido1<tm1Alm>	involves: 129X1/SvJ * BALB/c	N	21189261
MGI:4950076	M	MP:0004000	impaired passive avoidance behavior	Fmr1<tm1Usdn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	21220020
MGI:4950076	M	MP:0004851	increased testis weight	Fmr1<tm1Usdn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	21220020
MGI:4950076	M	MP:0002152	abnormal brain morphology	Fmr1<tm1Usdn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	21220020
MGI:4950076	M	MP:0001360	abnormal social investigation	Fmr1<tm1Usdn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	21220020
MGI:4950076	M	MP:0009936	abnormal dendritic spine morphology	Fmr1<tm1Usdn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	21220020
MGI:4950076	M	MP:0008143	abnormal dendrite morphology	Fmr1<tm1Usdn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	21220020
MGI:4950076	M	MP:0001364	decreased anxiety-related response	Fmr1<tm1Usdn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	21220020
MGI:4950076	M	MP:0031391	increased locomotor activity	Fmr1<tm1Usdn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	21220020
MGI:4950398	F	MP:0005389	reproductive system phenotype	Nxf3<tm1.1Jw>/Nxf3<tm1.1Jw>	involves: 129S4/SvJae * C57BL/6	Y	21308854
MGI:4950399	M	MP:0005389	reproductive system phenotype	Nxf3<tm1.2Jw>/Y	B6.Cg-Nxf3<tm1.2Jw>	Y	21308854
MGI:4950400	M	MP:0004852	decreased testis weight	Nxf2<tm1.2Jw> Nxf3<tm1.2Jw>/Y	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	21308854
MGI:4950400	M	MP:0002687	oligozoospermia	Nxf2<tm1.2Jw> Nxf3<tm1.2Jw>/Y	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	21308854
MGI:4950401	F	MP:0005389	reproductive system phenotype	Nxf3<tm1.2Jw>/Nxf3<tm1.2Jw>	involves: 129S4/SvJae * C57BL/6 * FVB/N	Y	21308854
MGI:4950463	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Tg(CAG-EGFP)D4Nagy/0,Xist<tm5.2Nbd>/Xist<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	N	21389056
MGI:4950464	M	MP:0004179	transmission ratio distortion	Xist<tm5.2Nbd>/Y	involves: 129P2/OlaHsd	N	21389056
MGI:4950465	F	MP:0003984	embryonic growth retardation	Xist<tm5.2Nbd>/Xist<+>	involves: 129P2/OlaHsd	N	21389056
MGI:4950465	F	MP:0001698	decreased embryo size	Xist<tm5.2Nbd>/Xist<+>	involves: 129P2/OlaHsd	N	21389056
MGI:4950465	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Xist<tm5.2Nbd>/Xist<+>	involves: 129P2/OlaHsd	N	21389056
MGI:4950465	F	MP:0000929	open neural tube	Xist<tm5.2Nbd>/Xist<+>	involves: 129P2/OlaHsd	N	21389056
MGI:4950465	F	MP:0003403	absent placental labyrinth	Xist<tm5.2Nbd>/Xist<+>	involves: 129P2/OlaHsd	N	21389056
MGI:4950465	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Xist<tm5.2Nbd>/Xist<+>	involves: 129P2/OlaHsd	N	21389056
MGI:4950466	F	MP:0002169	no abnormal phenotype detected	Xist<tm5.1Nbd>/Xist<tm5.1Nbd>	involves: 129P2/OlaHsd	N	21389056
MGI:4950467	M	MP:0002169	no abnormal phenotype detected	Xist<tm5.1Nbd>/Y	involves: 129P2/OlaHsd	N	21389056
MGI:4950686	M	MP:0001146	abnormal testis morphology	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950686	M	MP:0020550	multinucleated giant male germ cells	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950686	M	MP:0001147	small testis	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950686	M	MP:0001156	abnormal spermatogenesis	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950686	M	MP:0001153	small seminiferous tubules	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950686	F	MP:0001127	small ovary	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950686	F	MP:0002682	decreased mature ovarian follicle number	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950686	F	MP:0001126	abnormal ovary morphology	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950686	F	MP:0009661	abnormal pregnancy	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950686	M	MP:0002631	abnormal epididymis morphology	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950686	M	MP:0006379	abnormal spermatocyte morphology	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950686	M	MP:0001925	male infertility	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950686	M	MP:0001155	arrest of spermatogenesis	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950686	M	MP:0002685	abnormal spermatogonia proliferation	Dazap1<tm1Pyen>/Dazap1<tm1Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950688	M	MP:0001156	abnormal spermatogenesis	Dazap1<tm1.2Pyen>/Dazap1<tm1.2Pyen>	involves: 129S6/SvEvTac	N	18669443
MGI:4950700	F	MP:0004974	decreased regulatory T cell number	Foxp3<tm1(CD2/CD52)Shori>/Foxp3<tm1(CD2/CD52)Shori>	involves: C57BL/6	N	21460251
MGI:4950700	F	MP:0005617	increased susceptibility to type IV hypersensitivity reaction	Foxp3<tm1(CD2/CD52)Shori>/Foxp3<tm1(CD2/CD52)Shori>	involves: C57BL/6	N	21460251
MGI:4999589	F	MP:0000628	abnormal mammary gland development	Kdm4b<tm1.1Okad>/Kdm4b<tm1.1Okad>,Tg(MMTV-cre)1Mam/0	involves: 129P2/OlaHsd * FVB	N	21445275
MGI:4999589	F	MP:0000662	abnormal branching of the mammary ductal tree	Kdm4b<tm1.1Okad>/Kdm4b<tm1.1Okad>,Tg(MMTV-cre)1Mam/0	involves: 129P2/OlaHsd * FVB	N	21445275
MGI:4999590	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Kdm4b<tm1.1Okad>/Kdm4b<tm1.1Okad>	involves: 129P2/OlaHsd	N	21445275
MGI:4999644	M	MP:0010768	mortality/aging	Mecp2<tm1Bird>/Y,Tg(dlx5a-cre)1Mekk/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * CD-1 * FVB/N	Y	21068835
MGI:4999644	M	MP:0001489	decreased startle reflex	Mecp2<tm1Bird>/Y,Tg(dlx5a-cre)1Mekk/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * CD-1 * FVB/N	N	21068835
MGI:4999644	M	MP:0009141	increased prepulse inhibition	Mecp2<tm1Bird>/Y,Tg(dlx5a-cre)1Mekk/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * CD-1 * FVB/N	N	21068835
MGI:4999644	M	MP:0005388	respiratory system phenotype	Mecp2<tm1Bird>/Y,Tg(dlx5a-cre)1Mekk/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * CD-1 * FVB/N	Y	21068835
MGI:4999644	M	MP:0001447	abnormal nest building behavior	Mecp2<tm1Bird>/Y,Tg(dlx5a-cre)1Mekk/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * CD-1 * FVB/N	N	21068835
MGI:4999644	M	MP:0001405	impaired coordination	Mecp2<tm1Bird>/Y,Tg(dlx5a-cre)1Mekk/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * CD-1 * FVB/N	N	21068835
MGI:4999644	M	MP:0001409	increased stereotypic behavior	Mecp2<tm1Bird>/Y,Tg(dlx5a-cre)1Mekk/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * CD-1 * FVB/N	N	21068835
MGI:4999644	M	MP:0005386	behavior/neurological phenotype	Mecp2<tm1Bird>/Y,Tg(dlx5a-cre)1Mekk/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * CD-1 * FVB/N	Y	21068835
MGI:4999644	M	MP:0001360	abnormal social investigation	Mecp2<tm1Bird>/Y,Tg(dlx5a-cre)1Mekk/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * CD-1 * FVB/N	N	21068835
MGI:4999647	M	MP:0002272	abnormal nervous system electrophysiology	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0001489	decreased startle reflex	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0002083	premature death	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0009141	increased prepulse inhibition	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0001463	abnormal spatial learning	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0001405	impaired coordination	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0005586	decreased tidal volume	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0001402	decreased locomotor activity	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0003631	nervous system phenotype	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	Y	21068835
MGI:4999647	M	MP:0001409	increased stereotypic behavior	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0009435	abnormal miniature inhibitory postsynaptic currents	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0014274	decreased respiration	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0001513	limb grasping	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0010053	decreased grip strength	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0001360	abnormal social investigation	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0001441	increased grooming behavior	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0001957	apnea	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0001263	weight loss	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0001447	abnormal nest building behavior	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0005386	behavior/neurological phenotype	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	Y	21068835
MGI:4999647	M	MP:0001951	abnormal breathing pattern	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0001954	respiratory distress	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999647	M	MP:0001473	reduced long-term potentiation	Mecp2<tm1Bird>/Y,Tg(Slc32a1-cre)2.1Hzo/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * FVB/N	N	21068835
MGI:4999648	M	MP:0002272	abnormal nervous system electrophysiology	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	21068835
MGI:4999648	M	MP:0002064	seizures	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	21068835
MGI:4999648	M	MP:0009435	abnormal miniature inhibitory postsynaptic currents	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	21068835
MGI:4999649	M	MP:0010768	mortality/aging	Mecp2<tm1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	Y	21068835
MGI:4999649	M	MP:0005388	respiratory system phenotype	Mecp2<tm1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	Y	21068835
MGI:5002450	F	MP:0005386	behavior/neurological phenotype	Mecp2<tm1.1Vnar>/Mecp2<tm1.1Vnar>	B6N.129-Mecp2<tm1.1Vnar>	Y	MGI:4949877
MGI:5002450	F	MP:0000812	abnormal dentate gyrus morphology	Mecp2<tm1.1Vnar>/Mecp2<tm1.1Vnar>	B6N.129-Mecp2<tm1.1Vnar>	N	MGI:4949877
MGI:5002450	F	MP:0000886	abnormal cerebellar granule layer morphology	Mecp2<tm1.1Vnar>/Mecp2<tm1.1Vnar>	B6N.129-Mecp2<tm1.1Vnar>	N	MGI:4949877
MGI:5002450	F	MP:0000849	abnormal cerebellum morphology	Mecp2<tm1.1Vnar>/Mecp2<tm1.1Vnar>	B6N.129-Mecp2<tm1.1Vnar>	N	MGI:4949877
MGI:5002450	F	MP:0005378	growth/size/body region phenotype	Mecp2<tm1.1Vnar>/Mecp2<tm1.1Vnar>	B6N.129-Mecp2<tm1.1Vnar>	Y	MGI:4949877
MGI:5002450	F	MP:0004170	abnormal orbitofrontal cortex morphology	Mecp2<tm1.1Vnar>/Mecp2<tm1.1Vnar>	B6N.129-Mecp2<tm1.1Vnar>	N	MGI:4949877
MGI:5002450	M	MP:0001925	male infertility	Mecp2<tm1.1Vnar>/Mecp2<tm1.1Vnar>	B6N.129-Mecp2<tm1.1Vnar>	N	MGI:4949877
MGI:5002450	F	MP:0008143	abnormal dendrite morphology	Mecp2<tm1.1Vnar>/Mecp2<tm1.1Vnar>	B6N.129-Mecp2<tm1.1Vnar>	N	MGI:4949877
MGI:5002450	F	MP:0000819	abnormal olfactory bulb morphology	Mecp2<tm1.1Vnar>/Mecp2<tm1.1Vnar>	B6N.129-Mecp2<tm1.1Vnar>	N	MGI:4949877
MGI:5002450	F	MP:0000807	abnormal hippocampus morphology	Mecp2<tm1.1Vnar>/Mecp2<tm1.1Vnar>	B6N.129-Mecp2<tm1.1Vnar>	N	MGI:4949877
MGI:5002450	F	MP:0010768	mortality/aging	Mecp2<tm1.1Vnar>/Mecp2<tm1.1Vnar>	B6N.129-Mecp2<tm1.1Vnar>	Y	MGI:4949877
MGI:5002489	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Ncoa3<tm1Jxu>/Ncoa3<tm1Jxu>,Tg(MMTV-vHaras)SH1Led/0	involves: 129S6/SvEvTac * C57BL/6J * CD-1	N	14996752
MGI:5003280	M	MP:0001147	small testis	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0010948	abnormal double-strand DNA break repair	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	F	MP:0001923	reduced female fertility	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0006379	abnormal spermatocyte morphology	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0001925	male infertility	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0004852	decreased testis weight	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0005159	azoospermia	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0002675	asthenozoospermia	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0014052	increased male germ cell apoptosis	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0005169	abnormal male meiosis	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0001156	abnormal spermatogenesis	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0009230	abnormal sperm head morphology	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0020550	multinucleated giant male germ cells	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0008892	abnormal sperm flagellum morphology	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0002687	oligozoospermia	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0004930	small epididymis	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5003280	M	MP:0006380	abnormal spermatid morphology	Cul4a<tm1.2Pra>/Cul4a<tm1.2Pra>	Not Specified	N	21291880
MGI:5004869	F	MP:0001926	female infertility	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	involves: C57BL/6	N	21479251
MGI:5004869	F	MP:0009661	abnormal pregnancy	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	involves: C57BL/6	N	21479251
MGI:5004870	F	MP:0001926	female infertility	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<Gt(AJ0609)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	21479251
MGI:5006842	M	MP:0001806	decreased IgM level	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006842	M	MP:0009923	decreased transitional stage T1 B cell number	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006842	M	MP:0005344	increased circulating bilirubin level	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006842	M	MP:0008495	decreased IgG1 level	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006842	M	MP:0008215	decreased immature B cell number	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006842	M	MP:0008175	absent follicular B cells	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006842	M	MP:0005387	immune system phenotype	Atp11c<m1Btlr>/Y	involves: C57BL/6J	Y	21423172
MGI:5006842	M	MP:0009926	decreased transitional stage T2 B cell number	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006842	M	MP:0004978	decreased B-1 B cell number	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006842	M	MP:0008190	decreased transitional stage B cell number	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006842	M	MP:0008207	decreased B-2 B cell number	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006842	M	MP:0005387	immune system phenotype	Atp11c<m1Btlr>/Y	involves: C57BL/6J	Y	22761313
MGI:5006842	M	MP:0001807	decreased IgA level	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006842	M	MP:0005017	decreased B cell number	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	22761313
MGI:5006842	M	MP:0005017	decreased B cell number	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006842	M	MP:0010228	decreased transitional stage T3 B cell number	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006842	M	MP:0001802	arrested B cell differentiation	Atp11c<m1Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006843	F	MP:0005017	decreased B cell number	Atp11c<m1Btlr>/Atp11c<m1Btlr>	involves: C57BL/6J	N	22761313
MGI:5006843	F	MP:0005387	immune system phenotype	Atp11c<m1Btlr>/Atp11c<m1Btlr>	involves: C57BL/6J	Y	21423172
MGI:5006843	F	MP:0005387	immune system phenotype	Atp11c<m1Btlr>/Atp11c<m1Btlr>	involves: C57BL/6J	Y	22761313
MGI:5006844	M	MP:0005017	decreased B cell number	Atp11c<m1Btlr>/Y,Tg(IghmHyHEL10,IgkHyHEL10)4Ccg/0	involves: C57BL/6 * C57BL/6J * C57BL/6JSfdAnu	N	21423172
MGI:5006845	F	MP:0005017	decreased B cell number	Atp11c<m1Btlr>/Atp11c<m2Btlr>	involves: C57BL/6J	N	21423172
MGI:5006846	M	MP:0005387	immune system phenotype	Atp11c<m2Btlr>/Y	involves: C57BL/6J	Y	22761313
MGI:5006846	M	MP:0005017	decreased B cell number	Atp11c<m2Btlr>/Y	involves: C57BL/6J	N	21423172
MGI:5006846	M	MP:0005017	decreased B cell number	Atp11c<m2Btlr>/Y	involves: C57BL/6J	N	22761313
MGI:5006847	M	MP:0005017	decreased B cell number	Atp11c<m1Btlr>/Y,Tg(BCL2)22Wehi/0	involves: C57BL/6J * C57BL/6JWehi * SJL/Wehi	N	21423172
MGI:5006847	M	MP:0008181	increased marginal zone B cell number	Atp11c<m1Btlr>/Y,Tg(BCL2)22Wehi/0	involves: C57BL/6J * C57BL/6JWehi * SJL/Wehi	N	21423172
MGI:5006847	M	MP:0008174	decreased follicular B cell number	Atp11c<m1Btlr>/Y,Tg(BCL2)22Wehi/0	involves: C57BL/6J * C57BL/6JWehi * SJL/Wehi	N	21423172
MGI:5006847	M	MP:0008211	decreased mature B cell number	Atp11c<m1Btlr>/Y,Tg(BCL2)22Wehi/0	involves: C57BL/6J * C57BL/6JWehi * SJL/Wehi	N	21423172
MGI:5006960	M	MP:0008211	decreased mature B cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0003331	increased hepatocellular carcinoma incidence	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0005018	decreased T cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0005017	decreased B cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0005397	hematopoietic system phenotype	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	Y	21423173
MGI:5006960	M	MP:0005016	decreased lymphocyte cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0004978	decreased B-1 B cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0008215	decreased immature B cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0008209	decreased pre-B cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0008208	decreased pro-B cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0008207	decreased B-2 B cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0008174	decreased follicular B cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0008170	decreased B-1b cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0008168	decreased B-1a cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0002875	decreased erythrocyte cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0001577	anemia	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0000221	decreased leukocyte cell number	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0002144	abnormal B cell differentiation	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0001800	abnormal humoral immune response	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006960	M	MP:0005344	increased circulating bilirubin level	Atp11c<ambr>/Y	C57BL/6-Atp11c<ambr>	N	21423173
MGI:5006961	M	MP:0005017	decreased B cell number	Atp11c<ambr>/Y,Tg(H2-Ea-Il7)10Rhdr/0	involves: C57BL/6 * C57BL/6JApb * DBA/2	N	21423173
MGI:5006963	M	MP:0008215	decreased immature B cell number	Atp11c<ambr>/Y,Tg(Vav-BCL2)69Jad/0	involves: C57BL/6 * C57BL/6J * C57BL/6JApb	N	21423173
MGI:5006963	M	MP:0008209	decreased pre-B cell number	Atp11c<ambr>/Y,Tg(Vav-BCL2)69Jad/0	involves: C57BL/6 * C57BL/6J * C57BL/6JApb	N	21423173
MGI:5006963	M	MP:0005017	decreased B cell number	Atp11c<ambr>/Y,Tg(Vav-BCL2)69Jad/0	involves: C57BL/6 * C57BL/6J * C57BL/6JApb	N	21423173
MGI:5006965	M	MP:0008215	decreased immature B cell number	Atp11c<ambr>/Y,Tg(IghelMD4)4Ccg/0	involves: C57BL/6 * C57BL/6JApb	N	21423173
MGI:5006965	M	MP:0008208	decreased pro-B cell number	Atp11c<ambr>/Y,Tg(IghelMD4)4Ccg/0	involves: C57BL/6 * C57BL/6JApb	N	21423173
MGI:5006967	M	MP:0005017	decreased B cell number	Atp11c<m2Anu>/Y	C57BL/6JAnu-Atp11c<m2Anu>/AnuApb	N	21423173
MGI:5006981	M	MP:0005386	behavior/neurological phenotype	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	Y	21093492
MGI:5006981	M	MP:0005394	taste/olfaction phenotype	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	Y	21093492
MGI:5006981	M	MP:0001529	abnormal vocalization	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006981	M	MP:0002175	decreased brain weight	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006981	M	MP:0001354	increased aggression towards male mice	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006981	M	MP:0001394	circling	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006981	M	MP:0005409	darkened coat color	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006981	M	MP:0009142	decreased prepulse inhibition	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006981	M	MP:0001399	hyperactivity	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006981	M	MP:0001360	abnormal social investigation	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006981	M	MP:0002635	reduced sensorimotor gating	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006981	M	MP:0005377	hearing/vestibular/ear phenotype	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	Y	21093492
MGI:5006981	M	MP:0002738	hyperresponsive to tactile stimuli	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006981	M	MP:0001496	audiogenic seizures	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006981	M	MP:0005376	homeostasis/metabolism phenotype	Tg(Mov1/Tyr)OVE876BPay/Y	FVB/N-Tg(Mov1/Tyr)OVE876BPay	Y	21093492
MGI:5006985	F	MP:0001399	hyperactivity	Tg(Mov1/Tyr)OVE876BPay/Tg(Mov1/Tyr)OVE876BPay	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006985	F	MP:0001529	abnormal vocalization	Tg(Mov1/Tyr)OVE876BPay/Tg(Mov1/Tyr)OVE876BPay	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006985	F	MP:0009142	decreased prepulse inhibition	Tg(Mov1/Tyr)OVE876BPay/Tg(Mov1/Tyr)OVE876BPay	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006985	F	MP:0001496	audiogenic seizures	Tg(Mov1/Tyr)OVE876BPay/Tg(Mov1/Tyr)OVE876BPay	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006985	F	MP:0005366	variegated coat color	Tg(Mov1/Tyr)OVE876BPay/Tg(Mov1/Tyr)OVE876BPay	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5006985	F	MP:0002635	reduced sensorimotor gating	Tg(Mov1/Tyr)OVE876BPay/Tg(Mov1/Tyr)OVE876BPay	FVB/N-Tg(Mov1/Tyr)OVE876BPay	N	21093492
MGI:5007486	M	MP:0031369	prostate gland dorsolateral lobe hyperplasia	Acp3<tm1Pivi>/Acp3<tm1Pivi>	B6.Cg-Acp3<tm1Pivi>	N	24039861
MGI:5007486	M	MP:0001168	abnormal prostate gland epithelium morphology	Acp3<tm1Pivi>/Acp3<tm1Pivi>	B6.Cg-Acp3<tm1Pivi>	N	24039861
MGI:5007486	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Acp3<tm1Pivi>/Acp3<tm1Pivi>	B6.Cg-Acp3<tm1Pivi>	N	24039861
MGI:5007486	M	MP:0009381	abnormal prostate gland dorsolateral lobe morphology	Acp3<tm1Pivi>/Acp3<tm1Pivi>	B6.Cg-Acp3<tm1Pivi>	N	24039861
MGI:5007486	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Acp3<tm1Pivi>/Acp3<tm1Pivi>	B6.Cg-Acp3<tm1Pivi>	N	24039861
MGI:5007635	F	MP:0005391	vision/eye phenotype	Plxna3<tm1Matl>/Plxna3<tm1Matl>	involves: 129S1/Sv	Y	21270798
MGI:5007636	F	MP:0005391	vision/eye phenotype	Plxnb3<tm1Mom>/Plxnb3<tm1Mom>	involves: 129P2/OlaHsd	Y	21270798
MGI:5007681	F	MP:0006264	decreased systemic arterial systolic blood pressure	Agtr1a<tm1.1Cof>/Agtr1a<tm1.1Cof>,Hprt1<tm1(Pck1-cre)Vhh>/Hprt1<+>	involves: 129 * 129P2/OlaHsd	N	21459331
MGI:5007681	F	MP:0010108	abnormal renal water reabsorption	Agtr1a<tm1.1Cof>/Agtr1a<tm1.1Cof>,Hprt1<tm1(Pck1-cre)Vhh>/Hprt1<+>	involves: 129 * 129P2/OlaHsd	N	21459331
MGI:5007681	F	MP:0005528	decreased renal glomerular filtration rate	Agtr1a<tm1.1Cof>/Agtr1a<tm1.1Cof>,Hprt1<tm1(Pck1-cre)Vhh>/Hprt1<+>	involves: 129 * 129P2/OlaHsd	N	21459331
MGI:5007742	F	MP:0008000	increased ovary tumor incidence	Cul9<tm1.2Yxi>/Cul9<tm1.2Yxi>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21487039
MGI:5007925	M	MP:0003698	abnormal male reproductive system physiology	Mefv<tm2.1(MEFV)Chae>/Mefv<+>	chimera involves: 129S6/SvEvTac	N	21600797
MGI:5008182	F	MP:0001926	female infertility	Akr1a1<Gt(OST222400)Lex>/Akr1a1<Gt(OST222400)Lex>	B6.129S5-Akr1a1<Gt(OST222400)Lex>	N	20410296
MGI:5008263	M	MP:0008261	arrest of male meiosis	Tg(TSPY1-Figla)#Dean/?	FVB/N-Tg(TSPY1-Figla)#Dean	N	20479125
MGI:5008263	M	MP:0004901	decreased male germ cell number	Tg(TSPY1-Figla)#Dean/?	FVB/N-Tg(TSPY1-Figla)#Dean	N	20479125
MGI:5008263	M	MP:0009237	kinked sperm flagellum	Tg(TSPY1-Figla)#Dean/?	FVB/N-Tg(TSPY1-Figla)#Dean	N	20479125
MGI:5008263	M	MP:0002674	abnormal sperm motility	Tg(TSPY1-Figla)#Dean/?	FVB/N-Tg(TSPY1-Figla)#Dean	N	20479125
MGI:5008263	M	MP:0031620	abnormal chromatoid body morphology	Tg(TSPY1-Figla)#Dean/?	FVB/N-Tg(TSPY1-Figla)#Dean	N	20479125
MGI:5008263	M	MP:0002687	oligozoospermia	Tg(TSPY1-Figla)#Dean/?	FVB/N-Tg(TSPY1-Figla)#Dean	N	20479125
MGI:5008263	M	MP:0001154	seminiferous tubule degeneration	Tg(TSPY1-Figla)#Dean/?	FVB/N-Tg(TSPY1-Figla)#Dean	N	20479125
MGI:5008263	M	MP:0001147	small testis	Tg(TSPY1-Figla)#Dean/?	FVB/N-Tg(TSPY1-Figla)#Dean	N	20479125
MGI:5008263	M	MP:0006379	abnormal spermatocyte morphology	Tg(TSPY1-Figla)#Dean/?	FVB/N-Tg(TSPY1-Figla)#Dean	N	20479125
MGI:5008263	M	MP:0001925	male infertility	Tg(TSPY1-Figla)#Dean/?	FVB/N-Tg(TSPY1-Figla)#Dean	N	20479125
MGI:5008418	F	MP:0003329	amyloid beta deposits	Tg(APPswe,PSEN1dE9)85Dbo/0	B6.Cg-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax	N	24274089
MGI:5008586	M	MP:0000659	prostate gland hyperplasia	Gt(ROSA)26Sor<tm1(H1/tetO-RNAi:Pdpk1)Mrl>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21493594
MGI:5008586	M	MP:0010357	increased prostate gland tumor incidence	Gt(ROSA)26Sor<tm1(H1/tetO-RNAi:Pdpk1)Mrl>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21493594
MGI:5008586	M	MP:0003607	abnormal prostate gland physiology	Gt(ROSA)26Sor<tm1(H1/tetO-RNAi:Pdpk1)Mrl>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21493594
MGI:5008586	M	MP:0009738	enlarged prostate gland anterior lobe	Gt(ROSA)26Sor<tm1(H1/tetO-RNAi:Pdpk1)Mrl>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21493594
MGI:5008586	M	MP:0004961	increased prostate gland weight	Gt(ROSA)26Sor<tm1(H1/tetO-RNAi:Pdpk1)Mrl>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21493594
MGI:5008589	M	MP:0009738	enlarged prostate gland anterior lobe	Gt(ROSA)26Sor<tm2(H1/tetO-RNAi:Pdpk1)Mrl>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21493594
MGI:5008589	M	MP:0010357	increased prostate gland tumor incidence	Gt(ROSA)26Sor<tm2(H1/tetO-RNAi:Pdpk1)Mrl>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21493594
MGI:5008589	M	MP:0000659	prostate gland hyperplasia	Gt(ROSA)26Sor<tm2(H1/tetO-RNAi:Pdpk1)Mrl>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21493594
MGI:5008589	M	MP:0004961	increased prostate gland weight	Gt(ROSA)26Sor<tm2(H1/tetO-RNAi:Pdpk1)Mrl>/Gt(ROSA)26Sor<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	21493594
MGI:5008642	F	MP:0002169	no abnormal phenotype detected	Pof1b<tm1Toni>/Pof1b<tm1Toni>	B6.Cg-Pof1b<tm1Toni>	N	MGI:2655403
MGI:5008746	M	MP:0004852	decreased testis weight	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0002428	abnormal semicircular canal morphology	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0000042	abnormal organ of Corti morphology	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0001399	hyperactivity	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0001523	impaired righting response	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0002901	increased urine phosphate level	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0002687	oligozoospermia	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0008151	increased diameter of long bones	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0001967	deafness	Gy/Y	involves: 101/H * C3H/HeH	N	MGI:1889031
MGI:5008746	M	MP:0002102	abnormal ear morphology	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0004716	abnormal cochlear nerve morphology	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0001925	male infertility	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0001394	circling	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0001394	circling	Gy/Y	involves: 101/H * C3H/HeH	N	MGI:1889031
MGI:5008746	M	MP:0003723	abnormal long bone morphology	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0001262	decreased body weight	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0006358	absent pinna reflex	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0004362	cochlear hair cell degeneration	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0003150	detached tectorial membrane	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0002968	increased circulating alkaline phosphatase level	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0009445	osteomalacia	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0002187	abnormal fibula morphology	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0000150	abnormal rib morphology	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0001340	abnormal eyelid morphology	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0004686	decreased length of long bones	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0002730	head shaking	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0005251	blepharitis	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0002083	premature death	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0001265	decreased body size	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0004332	utricular degeneration	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0004329	vestibular saccular degeneration	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0004673	splayed ribs	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0011476	abnormal urine nucleotide level	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0000432	abnormal head morphology	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0002100	abnormal tooth morphology	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0000198	decreased circulating phosphate level	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008746	M	MP:0010924	abnormal osteoid morphology	Gy/Y	involves: 101/H * C3H/HeH	N	3460077
MGI:5008747	F	MP:0001967	deafness	Gy/Gy<+>	involves: 101/H * C3H/HeH	N	MGI:1889031
MGI:5008747	F	MP:0001262	decreased body weight	Gy/Gy<+>	involves: 101/H * C3H/HeH	N	3460077
MGI:5008747	F	MP:0001394	circling	Gy/Gy<+>	involves: 101/H * C3H/HeH	N	MGI:1889031
MGI:5008747	F	MP:0000198	decreased circulating phosphate level	Gy/Gy<+>	involves: 101/H * C3H/HeH	N	3460077
MGI:5008747	F	MP:0001394	circling	Gy/Gy<+>	involves: 101/H * C3H/HeH	N	3460077
MGI:5008747	F	MP:0003109	short femur	Gy/Gy<+>	involves: 101/H * C3H/HeH	N	3460077
MGI:5008997	M	MP:0011476	abnormal urine nucleotide level	Phex<Hyp>/Y	involves: C57BL/6	N	3460077
MGI:5008997	M	MP:0002968	increased circulating alkaline phosphatase level	Phex<Hyp>/Y	involves: C57BL/6	N	3460077
MGI:5008997	M	MP:0000198	decreased circulating phosphate level	Phex<Hyp>/Y	involves: C57BL/6	N	3460077
MGI:5008997	M	MP:0011447	abnormal renal glucose reabsorption	Phex<Hyp>/Y	involves: C57BL/6	N	3460077
MGI:5008997	M	MP:0002901	increased urine phosphate level	Phex<Hyp>/Y	involves: C57BL/6	N	3460077
MGI:5009006	M	MP:0004380	short frontal bone	Gy/Y	involves: 101/H * C3H/HeH * C57BL/6J	N	1962291
MGI:5009006	M	MP:0000440	domed cranium	Gy/Y	involves: 101/H * C3H/HeH * C57BL/6J	N	1962291
MGI:5009006	M	MP:0000091	short premaxilla	Gy/Y	involves: 101/H * C3H/HeH * C57BL/6J	N	1962291
MGI:5009006	M	MP:0000088	short mandible	Gy/Y	involves: 101/H * C3H/HeH * C57BL/6J	N	1962291
MGI:5009006	M	MP:0008525	decreased cranium height	Gy/Y	involves: 101/H * C3H/HeH * C57BL/6J	N	1962291
MGI:5009006	M	MP:0004471	short nasal bone	Gy/Y	involves: 101/H * C3H/HeH * C57BL/6J	N	1962291
MGI:5009006	M	MP:0000438	abnormal cranium morphology	Gy/Y	involves: 101/H * C3H/HeH * C57BL/6J	N	1962291
MGI:5009006	M	MP:0002835	abnormal cranial suture morphology	Gy/Y	involves: 101/H * C3H/HeH * C57BL/6J	N	1962291
MGI:5009008	M	MP:0001262	decreased body weight	Phex<Hyp>/Y	involves: C57BL/6J	N	8266820
MGI:5009008	M	MP:0008525	decreased cranium height	Phex<Hyp>/Y	involves: C57BL/6J	N	1962291
MGI:5009008	M	MP:0000440	domed cranium	Phex<Hyp>/Y	involves: C57BL/6J	N	1962291
MGI:5009008	M	MP:0000091	short premaxilla	Phex<Hyp>/Y	involves: C57BL/6J	N	1962291
MGI:5009008	M	MP:0002835	abnormal cranial suture morphology	Phex<Hyp>/Y	involves: C57BL/6J	N	1962291
MGI:5009008	M	MP:0011221	decreased intestinal calcium absorption	Phex<Hyp>/Y	involves: C57BL/6J	N	8266820
MGI:5009008	M	MP:0000088	short mandible	Phex<Hyp>/Y	involves: C57BL/6J	N	1962291
MGI:5009008	M	MP:0000198	decreased circulating phosphate level	Phex<Hyp>/Y	involves: C57BL/6J	N	8266820
MGI:5009008	M	MP:0004471	short nasal bone	Phex<Hyp>/Y	involves: C57BL/6J	N	1962291
MGI:5009008	M	MP:0004380	short frontal bone	Phex<Hyp>/Y	involves: C57BL/6J	N	1962291
MGI:5009008	M	MP:0000438	abnormal cranium morphology	Phex<Hyp>/Y	involves: C57BL/6J	N	1962291
MGI:5009009	F	MP:0000438	abnormal cranium morphology	Phex<Hyp>/Phex<Hyp>	involves: C57BL/6J	N	1962291
MGI:5009009	F	MP:0002835	abnormal cranial suture morphology	Phex<Hyp>/Phex<Hyp>	involves: C57BL/6J	N	1962291
MGI:5009009	F	MP:0000091	short premaxilla	Phex<Hyp>/Phex<Hyp>	involves: C57BL/6J	N	1962291
MGI:5009009	F	MP:0004380	short frontal bone	Phex<Hyp>/Phex<Hyp>	involves: C57BL/6J	N	1962291
MGI:5009009	F	MP:0000440	domed cranium	Phex<Hyp>/Phex<Hyp>	involves: C57BL/6J	N	1962291
MGI:5009009	F	MP:0008525	decreased cranium height	Phex<Hyp>/Phex<Hyp>	involves: C57BL/6J	N	1962291
MGI:5009009	F	MP:0000088	short mandible	Phex<Hyp>/Phex<Hyp>	involves: C57BL/6J	N	1962291
MGI:5009009	F	MP:0004471	short nasal bone	Phex<Hyp>/Phex<Hyp>	involves: C57BL/6J	N	1962291
MGI:5009021	F	MP:0001265	decreased body size	Ebp<Td-ho>/Ebp<+>	involves: C57BL/6J * M. spretus	N	9250864
MGI:5009021	F	MP:0001242	hyperkeratosis	Ebp<Td-ho>/Ebp<+>	involves: C57BL/6J * M. spretus	N	9250864
MGI:5009021	F	MP:0001262	decreased body weight	Ebp<Td-ho>/Ebp<+>	involves: C57BL/6J * M. spretus	N	9250864
MGI:5009021	F	MP:0008770	decreased survivor rate	Ebp<Td-ho>/Ebp<+>	involves: C57BL/6J * M. spretus	N	9250864
MGI:5009023	M	MP:0011091	prenatal lethality, complete penetrance	Ebp<Td-ho>/Y	involves: C57BL/6J * M. spretus	N	9250864
MGI:5009024	M	MP:0004229	abnormal embryonic erythropoiesis	Ebp<Td-ho>/Y	(CKH.Cg-Ebp<Td-ho> x NJL)F1	N	10987663
MGI:5009024	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Ebp<Td-ho>/Y	(CKH.Cg-Ebp<Td-ho> x NJL)F1	N	9250864
MGI:5009024	M	MP:0004230	abnormal embryonic erythrocyte morphology	Ebp<Td-ho>/Y	(CKH.Cg-Ebp<Td-ho> x NJL)F1	N	10987663
MGI:5009024	M	MP:0003396	abnormal embryonic hematopoiesis	Ebp<Td-ho>/Y	(CKH.Cg-Ebp<Td-ho> x NJL)F1	N	10987663
MGI:5009025	F	MP:0011221	decreased intestinal calcium absorption	Phex<Hyp>/Phex<+>	involves: C57BL/6J	N	8266820
MGI:5009025	F	MP:0001262	decreased body weight	Phex<Hyp>/Phex<+>	involves: C57BL/6J	N	8266820
MGI:5009025	F	MP:0000198	decreased circulating phosphate level	Phex<Hyp>/Phex<+>	involves: C57BL/6J	N	8266820
MGI:5009026	M	MP:0000198	decreased circulating phosphate level	Phex<Hyp>/Y	involves: C3H/HeSnJ * C57BL/6J	N	8266820
MGI:5009026	M	MP:0001666	abnormal intestinal absorption	Phex<Hyp>/Y	involves: C3H/HeSnJ * C57BL/6J	N	8266820
MGI:5009027	F	MP:0001666	abnormal intestinal absorption	Phex<Hyp>/Phex<Hyp>	involves: C3H/HeSnJ * C57BL/6J	N	8266820
MGI:5009027	F	MP:0000198	decreased circulating phosphate level	Phex<Hyp>/Phex<Hyp>	involves: C3H/HeSnJ * C57BL/6J	N	8266820
MGI:5009028	M	MP:0000198	decreased circulating phosphate level	Gy/Y	B6.Cg-Gy	N	8266820
MGI:5009028	M	MP:0011221	decreased intestinal calcium absorption	Gy/Y	B6.Cg-Gy	N	8266820
MGI:5009028	M	MP:0004231	abnormal calcium ion homeostasis	Gy/Y	B6.Cg-Gy	N	8266820
MGI:5009029	F	MP:0000198	decreased circulating phosphate level	Gy/Gy	B6.Cg-Gy	N	8266820
MGI:5009029	F	MP:0011221	decreased intestinal calcium absorption	Gy/Gy	B6.Cg-Gy	N	8266820
MGI:5009030	M	MP:0001262	decreased body weight	Gy/Y	involves: 101/H * C3H/HeH * C3H/HeSnJ * C57BL/6J	N	8266820
MGI:5009030	M	MP:0011221	decreased intestinal calcium absorption	Gy/Y	involves: 101/H * C3H/HeH * C3H/HeSnJ * C57BL/6J	N	8266820
MGI:5009030	M	MP:0004231	abnormal calcium ion homeostasis	Gy/Y	involves: 101/H * C3H/HeH * C3H/HeSnJ * C57BL/6J	N	8266820
MGI:5009030	M	MP:0000198	decreased circulating phosphate level	Gy/Y	involves: 101/H * C3H/HeH * C3H/HeSnJ * C57BL/6J	N	8266820
MGI:5009031	F	MP:0011221	decreased intestinal calcium absorption	Gy/Gy	involves: 101/H * C3H/HeH * C3H/HeSnJ * C57BL/6J	N	8266820
MGI:5009031	F	MP:0001262	decreased body weight	Gy/Gy	involves: 101/H * C3H/HeH * C3H/HeSnJ * C57BL/6J	N	8266820
MGI:5009031	F	MP:0000198	decreased circulating phosphate level	Gy/Gy	involves: 101/H * C3H/HeH * C3H/HeSnJ * C57BL/6J	N	8266820
MGI:5009321	M	MP:0006262	increased testis tumor incidence	Men1<tm1Zqw>/Men1<+>	involves: 129/Sv * 129P2/OlaHsd	N	12819299
MGI:5009321	M	MP:0009592	increased Leydig cell tumor incidence	Men1<tm1Zqw>/Men1<+>	involves: 129/Sv * 129P2/OlaHsd	N	12819299
MGI:5009321	M	MP:0001148	enlarged testis	Men1<tm1Zqw>/Men1<+>	involves: 129/Sv * 129P2/OlaHsd	N	12819299
MGI:5009321	F	MP:0008000	increased ovary tumor incidence	Men1<tm1Zqw>/Men1<+>	involves: 129/Sv * 129P2/OlaHsd	N	12819299
MGI:5009321	F	MP:0004832	enlarged ovary	Men1<tm1Zqw>/Men1<+>	involves: 129/Sv * 129P2/OlaHsd	N	12819299
MGI:5009456	M	MP:0001147	small testis	Syce3<tm1Rben>/Syce3<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21637789
MGI:5009456	F	MP:0001127	small ovary	Syce3<tm1Rben>/Syce3<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21637789
MGI:5009456	M	MP:0001925	male infertility	Syce3<tm1Rben>/Syce3<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21637789
MGI:5009456	M	MP:0005159	azoospermia	Syce3<tm1Rben>/Syce3<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21637789
MGI:5009456	F	MP:0001926	female infertility	Syce3<tm1Rben>/Syce3<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21637789
MGI:5009456	F	MP:0005168	abnormal female meiosis	Syce3<tm1Rben>/Syce3<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21637789
MGI:5009456	M	MP:0001156	abnormal spermatogenesis	Syce3<tm1Rben>/Syce3<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21637789
MGI:5009456	M	MP:0005169	abnormal male meiosis	Syce3<tm1Rben>/Syce3<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21637789
MGI:5009456	F	MP:0001132	absent mature ovarian follicles	Syce3<tm1Rben>/Syce3<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21637789
MGI:5009456	F	MP:0001126	abnormal ovary morphology	Syce3<tm1Rben>/Syce3<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21637789
MGI:5009456	M	MP:0001155	arrest of spermatogenesis	Syce3<tm1Rben>/Syce3<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21637789
MGI:5009703	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Ar<tm1Verh>/Y,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * DBA/2	N	21620777
MGI:5013405	F	MP:0004047	abnormal milk composition	Tg(CSN2-fat-1)1Vane/0	involves: C57BL/6 * DBA	N	16840637
MGI:5013473	F	MP:0003436	decreased susceptibility to induced arthritis	Bmx<tm1Ali>/Bmx<tm1Ali>	involves: 129S1/Sv * 129X1/SvJ	N	21471444
MGI:5013474	F	MP:0005390	skeleton phenotype	Bmx<tm1.1Npa>/Bmx<tm1.1Npa>	BALB/c-Bmx<tm1.1Npa>	Y	21471444
MGI:5013558	M	MP:0008280	abnormal male germ cell apoptosis	Hormad1<tm1Atot>/Hormad1<tm1Atot>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013558	F	MP:0014445	abnormal spindle assembly in female meiosis	Hormad1<tm1Atot>/Hormad1<tm1Atot>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013558	F	MP:0014443	impaired polar body extrusion	Hormad1<tm1Atot>/Hormad1<tm1Atot>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013558	M	MP:0001155	arrest of spermatogenesis	Hormad1<tm1Atot>/Hormad1<tm1Atot>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013558	F	MP:0001926	female infertility	Hormad1<tm1Atot>/Hormad1<tm1Atot>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013558	M	MP:0005169	abnormal male meiosis	Hormad1<tm1Atot>/Hormad1<tm1Atot>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013558	M	MP:0005159	azoospermia	Hormad1<tm1Atot>/Hormad1<tm1Atot>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013558	F	MP:0005168	abnormal female meiosis	Hormad1<tm1Atot>/Hormad1<tm1Atot>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013558	M	MP:0001925	male infertility	Hormad1<tm1Atot>/Hormad1<tm1Atot>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013559	M	MP:0005169	abnormal male meiosis	Hormad1<tm1Atot>/Hormad1<tm1Atot>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013559	F	MP:0005168	abnormal female meiosis	Hormad1<tm1Atot>/Hormad1<tm1Atot>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013562	F	MP:0001926	female infertility	Hormad1<tm1.2Atot>/Hormad1<tm1.2Atot>	involves: 129/Sv * BALB/c * C57BL/6 * SJL	N	21478856
MGI:5013562	F	MP:0005389	reproductive system phenotype	Hormad1<tm1.2Atot>/Hormad1<tm1.2Atot>	involves: 129/Sv * BALB/c * C57BL/6 * SJL	Y	21478856
MGI:5013562	M	MP:0008280	abnormal male germ cell apoptosis	Hormad1<tm1.2Atot>/Hormad1<tm1.2Atot>	involves: 129/Sv * BALB/c * C57BL/6 * SJL	N	21478856
MGI:5013562	M	MP:0005159	azoospermia	Hormad1<tm1.2Atot>/Hormad1<tm1.2Atot>	involves: 129/Sv * BALB/c * C57BL/6 * SJL	N	21478856
MGI:5013562	F	MP:0014443	impaired polar body extrusion	Hormad1<tm1.2Atot>/Hormad1<tm1.2Atot>	involves: 129/Sv * BALB/c * C57BL/6 * SJL	N	21478856
MGI:5013562	F	MP:0005168	abnormal female meiosis	Hormad1<tm1.2Atot>/Hormad1<tm1.2Atot>	involves: 129/Sv * BALB/c * C57BL/6 * SJL	N	21478856
MGI:5013562	M	MP:0001155	arrest of spermatogenesis	Hormad1<tm1.2Atot>/Hormad1<tm1.2Atot>	involves: 129/Sv * BALB/c * C57BL/6 * SJL	N	21478856
MGI:5013562	M	MP:0001925	male infertility	Hormad1<tm1.2Atot>/Hormad1<tm1.2Atot>	involves: 129/Sv * BALB/c * C57BL/6 * SJL	N	21478856
MGI:5013562	F	MP:0014445	abnormal spindle assembly in female meiosis	Hormad1<tm1.2Atot>/Hormad1<tm1.2Atot>	involves: 129/Sv * BALB/c * C57BL/6 * SJL	N	21478856
MGI:5013562	M	MP:0005169	abnormal male meiosis	Hormad1<tm1.2Atot>/Hormad1<tm1.2Atot>	involves: 129/Sv * BALB/c * C57BL/6 * SJL	N	21478856
MGI:5013563	F	MP:0005168	abnormal female meiosis	Hormad1<tm1.2Atot>/Hormad1<tm1.2Atot>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129/Sv * BALB/c * C57BL/6 * SJL	N	21478856
MGI:5013563	M	MP:0005169	abnormal male meiosis	Hormad1<tm1.2Atot>/Hormad1<tm1.2Atot>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129/Sv * BALB/c * C57BL/6 * SJL	N	21478856
MGI:5013563	M	MP:0005169	abnormal male meiosis	Hormad1<tm1.2Atot>/Hormad1<tm1.2Atot>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129/Sv * BALB/c * C57BL/6 * SJL	N	32345962
MGI:5013565	M	MP:0001155	arrest of spermatogenesis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013565	F	MP:0005168	abnormal female meiosis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013565	F	MP:0031474	increased female germ cell apoptosis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013565	F	MP:0005431	decreased oocyte number	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013566	M	MP:0001155	arrest of spermatogenesis	Spo11<tm1Mjn>/Spo11<tm1Mjn>,Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6JOlaHsd	N	21478856
MGI:5013567	F	MP:0003231	abnormal placenta vasculature	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	20858757
MGI:5013567	F	MP:0008256	abnormal myometrium morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	20858757
MGI:5013567	F	MP:0002676	uterus hyperplasia	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	20858757
MGI:5013567	F	MP:0008876	decreased uterine NK cell number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	20858757
MGI:5013567	M	MP:0005389	reproductive system phenotype	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	Y	22791749
MGI:5013567	F	MP:0004256	abnormal maternal decidual layer morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	20858757
MGI:5013567	F	MP:0001923	reduced female fertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	20858757
MGI:5013567	F	MP:0004896	abnormal endometrium morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	20858757
MGI:5013567	F	MP:0009092	endometrium hyperplasia	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	20858757
MGI:5013567	F	MP:0013399	endometrium fibrosis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	20858757
MGI:5013567	F	MP:0001716	abnormal placenta labyrinth morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	20858757
MGI:5013602	M	MP:0003607	abnormal prostate gland physiology	Cop1<tm1.1Vmd>/Cop1<tm2.1Vmd>,Tg(CAG-cre/Esr1*)5Amc/0	involves: C57BL/6 * C57BL/6N * CBA	N	21572435
MGI:5013603	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Cop1<tm2.1Vmd>/Cop1<+>,Tg(Pbsn-cre)4Prb/0	B6N.CgCop1<tm2.1Vmd> Pten<tm1Hwu> Tg(Pbsn-cre)4Prb	N	21572435
MGI:5013603	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Cop1<tm2.1Vmd>/Cop1<+>,Tg(Pbsn-cre)4Prb/0	B6N.CgCop1<tm2.1Vmd> Pten<tm1Hwu> Tg(Pbsn-cre)4Prb	N	21572435
MGI:5013604	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Cop1<tm2.1Vmd>/Cop1<tm2.1Vmd>,Tg(Pbsn-cre)4Prb/0	B6N.CgCop1<tm2.1Vmd> Pten<tm1Hwu> Tg(Pbsn-cre)4Prb	N	21572435
MGI:5013604	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Cop1<tm2.1Vmd>/Cop1<tm2.1Vmd>,Tg(Pbsn-cre)4Prb/0	B6N.CgCop1<tm2.1Vmd> Pten<tm1Hwu> Tg(Pbsn-cre)4Prb	N	21572435
MGI:5013605	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Cop1<tm2.1Vmd>/Cop1<tm2.1Vmd>,Tg(Pbsn-cre)4Prb/0	B6N.Cg-Cop1<tm2.1Vmd> Tg(Pbsn-cre)4Prb	N	21572435
MGI:5013605	M	MP:0003607	abnormal prostate gland physiology	Cop1<tm2.1Vmd>/Cop1<tm2.1Vmd>,Tg(Pbsn-cre)4Prb/0	B6N.Cg-Cop1<tm2.1Vmd> Tg(Pbsn-cre)4Prb	N	21572435
MGI:5013605	M	MP:0000659	prostate gland hyperplasia	Cop1<tm2.1Vmd>/Cop1<tm2.1Vmd>,Tg(Pbsn-cre)4Prb/0	B6N.Cg-Cop1<tm2.1Vmd> Tg(Pbsn-cre)4Prb	N	21572435
MGI:5013606	M	MP:0000659	prostate gland hyperplasia	Cop1<tm2.1Vmd>/Cop1<+>,Tg(Pbsn-cre)4Prb/0	B6N.Cg-Cop1<tm2.1Vmd> Tg(Pbsn-cre)4Prb	N	21572435
MGI:5013714	M	MP:0001393	ataxia	Atp7a<Mo-ml>/Y	C3Hf/He	N	9166584
MGI:5013714	M	MP:0011110	preweaning lethality, incomplete penetrance	Atp7a<Mo-ml>/Y	C3Hf/He	N	MGI:5013588
MGI:5013714	M	MP:0002826	tonic seizures	Atp7a<Mo-ml>/Y	C3Hf/He	N	9166584
MGI:5013714	M	MP:0001731	abnormal postnatal growth	Atp7a<Mo-ml>/Y	C3Hf/He	N	9166584
MGI:5013714	M	MP:0005171	absent coat pigmentation	Atp7a<Mo-ml>/Y	C3Hf/He	N	MGI:5013588
MGI:5013714	M	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-ml>/Y	C3Hf/He	N	MGI:5013588
MGI:5013714	M	MP:0001274	curly vibrissae	Atp7a<Mo-ml>/Y	C3Hf/He	N	9166584
MGI:5013714	M	MP:0010769	abnormal survival	Atp7a<Mo-ml>/Y	C3Hf/He	N	MGI:5013588
MGI:5013714	M	MP:0005150	cachexia	Atp7a<Mo-ml>/Y	C3Hf/He	N	MGI:5013588
MGI:5013722	F	MP:0010016	variable depigmentation	Atp7a<Mo-ml>/Atp7a<+>	C3Hf/He	N	MGI:5013588
MGI:5013723	M	MP:0011110	preweaning lethality, incomplete penetrance	Atp7a<Mo-ml>/Y	involves: C3Hf/He * C57BL/6	N	MGI:5013588
MGI:5013821	F	MP:0009669	abnormal postimplantation uterine environment	Tlr3<tm1Flv>/Tlr3<tm1Flv>	involves: 129S1/Sv	N	19239422
MGI:5013821	F	MP:0009661	abnormal pregnancy	Tlr3<tm1Flv>/Tlr3<tm1Flv>	involves: 129S1/Sv	N	19239422
MGI:5013913	F	MP:0001382	abnormal nursing	Tg(MMTV-ERBB2*,-luc)6180Aami/0	FVB-Tg(MMTV-ERBB2*,-luc)6180Aami	N	21559085
MGI:5013919	F	MP:0001926	female infertility	Pdpk1<tm1Maka>/Pdpk1<tm1Maka>,Tg(Zp3-cre)93Knw/0	involves: 129S4/SvJae * C57BL/6J	N	20930845
MGI:5013960	F	MP:0008000	increased ovary tumor incidence	Pinx1<tm1.1Kplu>/Pinx1<+>,Trp53<tm1Brd>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	N	21436583
MGI:5014340	M	MP:0004777	abnormal phospholipid level	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0006380	abnormal spermatid morphology	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0001156	abnormal spermatogenesis	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0008892	abnormal sperm flagellum morphology	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0001925	male infertility	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0002079	increased circulating insulin level	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0002675	asthenozoospermia	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0011174	lipodystrophy	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0001146	abnormal testis morphology	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0005178	increased circulating cholesterol level	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0001932	abnormal spermiogenesis	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0009230	abnormal sperm head morphology	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0002687	oligozoospermia	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0005578	teratozoospermia	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014340	M	MP:0006362	abnormal male germ cell morphology	Bscl2<tm1.2Gliu>/Bscl2<tm1.2Gliu>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	N	24778225
MGI:5014516	F	MP:0008000	increased ovary tumor incidence	Kras<tm4Tyj>/Kras<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae	N	20505730
MGI:5014832	F	MP:0008000	increased ovary tumor incidence	Trp53<tm1.2Awbr>/Trp53<tm1.2Awbr>	involves: C57BL/6	N	21411755
MGI:5014833	F	MP:0008000	increased ovary tumor incidence	Trp53<tm1.2Awbr>/Trp53<+>	involves: C57BL/6	N	21411755
MGI:5049884	M	MP:0002169	no abnormal phenotype detected	Porcn<tm1.1Lcm>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21768372
MGI:5049885	F	MP:0002169	no abnormal phenotype detected	Porcn<tm1.1Lcm>/Porcn<tm1.1Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21768372
MGI:5049886	M	MP:0011099	lethality throughout fetal growth and development, complete penetrance	Porcn<tm1.1Lcm>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049886	M	MP:0001680	abnormal mesoderm development	Porcn<tm1.1Lcm>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049887	F	MP:0003815	hairless	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049887	F	MP:0004360	absent ulna	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049887	F	MP:0001244	thin dermal layer	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049887	F	MP:0000592	short tail	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049887	F	MP:0004323	sternum hypoplasia	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049887	F	MP:0003052	omphalocele	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049887	F	MP:0003704	abnormal hair follicle development	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049887	F	MP:0004073	caudal body truncation	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049887	F	MP:0011089	perinatal lethality, complete penetrance	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049887	F	MP:0000572	abnormal autopod morphology	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049887	F	MP:0001265	decreased body size	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049887	F	MP:0010771	integument phenotype	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	Y	21768372
MGI:5049887	F	MP:0000111	cleft palate	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049887	F	MP:0002111	abnormal tail morphology	Porcn<tm1.1Lcm>/Porcn<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21768372
MGI:5049888	M	MP:0000565	oligodactyly	Porcn<tm1.1Lcm>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL/J	N	21768372
MGI:5049888	M	MP:0000547	short limbs	Porcn<tm1.1Lcm>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL/J	N	21768372
MGI:5049889	M	MP:0014291	decreased autopod size	Porcn<tm1.1Lcm>/Y,Tg(Msx2-cre)5Rem/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21768372
MGI:5049889	M	MP:0002060	abnormal skin morphology	Porcn<tm1.1Lcm>/Y,Tg(Msx2-cre)5Rem/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21768372
MGI:5049889	M	MP:0000564	syndactyly	Porcn<tm1.1Lcm>/Y,Tg(Msx2-cre)5Rem/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21768372
MGI:5049889	M	MP:0001243	abnormal dermal layer morphology	Porcn<tm1.1Lcm>/Y,Tg(Msx2-cre)5Rem/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21768372
MGI:5050109	F	MP:0001926	female infertility	Hbb<d4>/Hbb<d4>	involves: 101/H	N	3839762
MGI:5050828	M	MP:0002631	abnormal epididymis morphology	Tk1<tm1Vnd>/Tk1<tm1Vnd>	involves: 129P2/OlaHsd * C57BL/6	N	12559842
MGI:5050828	M	MP:0001156	abnormal spermatogenesis	Tk1<tm1Vnd>/Tk1<tm1Vnd>	involves: 129P2/OlaHsd * C57BL/6	N	12559842
MGI:5051637	F	MP:0005376	homeostasis/metabolism phenotype	Gpr119<tm1Jleo>/Gpr119<tm1Jleo>	Not Specified	Y	17289847
MGI:5051637	F	MP:0005379	endocrine/exocrine gland phenotype	Gpr119<tm1Jleo>/Gpr119<tm1Jleo>	Not Specified	Y	17289847
MGI:5051637	F	MP:0005378	growth/size/body region phenotype	Gpr119<tm1Jleo>/Gpr119<tm1Jleo>	Not Specified	Y	17289847
MGI:5051914	M	MP:0003698	abnormal male reproductive system physiology	Ar<tm1Verh>/Y,Rnase10<tm1(cre)Hht>/Rnase10<+>	involves: 129S7/SvEvBrd * C57BL/6	N	21084446
MGI:5051914	M	MP:0003205	testicular atrophy	Ar<tm1Verh>/Y,Rnase10<tm1(cre)Hht>/Rnase10<+>	involves: 129S7/SvEvBrd * C57BL/6	N	21084446
MGI:5051914	M	MP:0001148	enlarged testis	Ar<tm1Verh>/Y,Rnase10<tm1(cre)Hht>/Rnase10<+>	involves: 129S7/SvEvBrd * C57BL/6	N	21084446
MGI:5051914	M	MP:0001146	abnormal testis morphology	Ar<tm1Verh>/Y,Rnase10<tm1(cre)Hht>/Rnase10<+>	involves: 129S7/SvEvBrd * C57BL/6	N	21084446
MGI:5051914	M	MP:0002660	abnormal caput epididymis morphology	Ar<tm1Verh>/Y,Rnase10<tm1(cre)Hht>/Rnase10<+>	involves: 129S7/SvEvBrd * C57BL/6	N	21084446
MGI:5051914	M	MP:0004933	abnormal epididymis epithelium morphology	Ar<tm1Verh>/Y,Rnase10<tm1(cre)Hht>/Rnase10<+>	involves: 129S7/SvEvBrd * C57BL/6	N	21084446
MGI:5051914	M	MP:0001154	seminiferous tubule degeneration	Ar<tm1Verh>/Y,Rnase10<tm1(cre)Hht>/Rnase10<+>	involves: 129S7/SvEvBrd * C57BL/6	N	21084446
MGI:5051914	M	MP:0001925	male infertility	Ar<tm1Verh>/Y,Rnase10<tm1(cre)Hht>/Rnase10<+>	involves: 129S7/SvEvBrd * C57BL/6	N	21084446
MGI:5051914	M	MP:0009198	abnormal male genitalia morphology	Ar<tm1Verh>/Y,Rnase10<tm1(cre)Hht>/Rnase10<+>	involves: 129S7/SvEvBrd * C57BL/6	N	21084446
MGI:5051914	M	MP:0001875	testis inflammation	Ar<tm1Verh>/Y,Rnase10<tm1(cre)Hht>/Rnase10<+>	involves: 129S7/SvEvBrd * C57BL/6	N	21084446
MGI:5051914	M	MP:0002631	abnormal epididymis morphology	Ar<tm1Verh>/Y,Rnase10<tm1(cre)Hht>/Rnase10<+>	involves: 129S7/SvEvBrd * C57BL/6	N	21084446
MGI:5051914	M	MP:0004934	epididymis epithelium degeneration	Ar<tm1Verh>/Y,Rnase10<tm1(cre)Hht>/Rnase10<+>	involves: 129S7/SvEvBrd * C57BL/6	N	21084446
MGI:5051961	M	MP:0006380	abnormal spermatid morphology	Kdm4d<tm1Zuk>/Kdm4d<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	21293030
MGI:5051961	M	MP:0008280	abnormal male germ cell apoptosis	Kdm4d<tm1Zuk>/Kdm4d<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	21293030
MGI:5051961	M	MP:0001148	enlarged testis	Kdm4d<tm1Zuk>/Kdm4d<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	21293030
MGI:5051961	M	MP:0006308	enlarged seminiferous tubules	Kdm4d<tm1Zuk>/Kdm4d<tm1Zuk>	involves: 129S7/SvEvBrd * C57BL/6J	N	21293030
MGI:5052044	F	MP:0004902	abnormal uterus size	Phb1<tm1.1Bwo>/Phb1<tm1.1Bwo>,Pgr<tm2(cre)Lyd>/?	involves: 129S7/SvEvBrd * C57BL/6	N	21209023
MGI:5052044	F	MP:0009088	thin uterine horn	Phb1<tm1.1Bwo>/Phb1<tm1.1Bwo>,Pgr<tm2(cre)Lyd>/?	involves: 129S7/SvEvBrd * C57BL/6	N	21209023
MGI:5052044	F	MP:0004905	decreased uterus weight	Phb1<tm1.1Bwo>/Phb1<tm1.1Bwo>,Pgr<tm2(cre)Lyd>/?	involves: 129S7/SvEvBrd * C57BL/6	N	21209023
MGI:5052044	F	MP:0004896	abnormal endometrium morphology	Phb1<tm1.1Bwo>/Phb1<tm1.1Bwo>,Pgr<tm2(cre)Lyd>/?	involves: 129S7/SvEvBrd * C57BL/6	N	21209023
MGI:5052044	F	MP:0001926	female infertility	Phb1<tm1.1Bwo>/Phb1<tm1.1Bwo>,Pgr<tm2(cre)Lyd>/?	involves: 129S7/SvEvBrd * C57BL/6	N	21209023
MGI:5052044	F	MP:0009091	endometrium hypoplasia	Phb1<tm1.1Bwo>/Phb1<tm1.1Bwo>,Pgr<tm2(cre)Lyd>/?	involves: 129S7/SvEvBrd * C57BL/6	N	21209023
MGI:5052044	F	MP:0001120	abnormal uterus morphology	Phb1<tm1.1Bwo>/Phb1<tm1.1Bwo>,Pgr<tm2(cre)Lyd>/?	involves: 129S7/SvEvBrd * C57BL/6	N	21209023
MGI:5052062	F	MP:0001923	reduced female fertility	Sfrp4<tm1.1Blan>/Sfrp4<tm1.1Blan>	involves: C57BL/6	N	21427221
MGI:5052138	F	MP:0006271	abnormal involution of the mammary gland	Gt(ROSA)26Sor<tm1(CAG-PIK3CA*H1047R,-EGFP)Balj>/Gt(ROSA)26Sor<+>,Tg(Wap-cre)1Gsc/0	involves: BALB/c * C57BL/6 * FVB/N	N	21482677
MGI:5052332	F	MP:0004856	decreased ovary weight	Gt(ROSA)26Sor<tm1(DTA)Riet>/Gt(ROSA)26Sor<+>,Kiss1r<tm1.1(cre)Uboe>/Kiss1r<+>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * SJL	N	21516099
MGI:5052332	F	MP:0003531	abnormal vagina development	Gt(ROSA)26Sor<tm1(DTA)Riet>/Gt(ROSA)26Sor<+>,Kiss1r<tm1.1(cre)Uboe>/Kiss1r<+>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * SJL	N	21516099
MGI:5052334	F	MP:0001926	female infertility	Gt(ROSA)26Sor<tm1(HBEGF)Awai>/Gt(ROSA)26Sor<+>,Kiss1<tm1.1(cre)Uboe>/Kiss1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL	N	21516099
MGI:5052334	F	MP:0009017	prolonged estrus	Gt(ROSA)26Sor<tm1(HBEGF)Awai>/Gt(ROSA)26Sor<+>,Kiss1<tm1.1(cre)Uboe>/Kiss1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL	N	21516099
MGI:5052334	F	MP:0009011	prolonged diestrus	Gt(ROSA)26Sor<tm1(HBEGF)Awai>/Gt(ROSA)26Sor<+>,Kiss1<tm1.1(cre)Uboe>/Kiss1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL	N	21516099
MGI:5052334	F	MP:0001927	abnormal estrous cycle	Gt(ROSA)26Sor<tm1(HBEGF)Awai>/Gt(ROSA)26Sor<+>,Kiss1<tm1.1(cre)Uboe>/Kiss1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL	N	21516099
MGI:5052335	F	MP:0004856	decreased ovary weight	Gt(ROSA)26Sor<tm1(DTA)Riet>/Gt(ROSA)26Sor<+>,Kiss1<tm1.1(cre)Uboe>/Kiss1<+>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	21516099
MGI:5052335	F	MP:0003531	abnormal vagina development	Gt(ROSA)26Sor<tm1(DTA)Riet>/Gt(ROSA)26Sor<+>,Kiss1<tm1.1(cre)Uboe>/Kiss1<+>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	21516099
MGI:5056318	F	MP:0005168	abnormal female meiosis	Tg(Zp3-cre)93Knw/0,Ttk<tm1Katj>/Ttk<tm1Katj>	involves: 129 * C57BL/6 * C57BL/6J	N	21558374
MGI:5056318	F	MP:0014444	enhanced polar body extrusion	Tg(Zp3-cre)93Knw/0,Ttk<tm1Katj>/Ttk<tm1Katj>	involves: 129 * C57BL/6 * C57BL/6J	N	21558374
MGI:5056318	F	MP:0001923	reduced female fertility	Tg(Zp3-cre)93Knw/0,Ttk<tm1Katj>/Ttk<tm1Katj>	involves: 129 * C57BL/6 * C57BL/6J	N	21558374
MGI:5056430	M	MP:0001147	small testis	Epb41l2<Gt(AL0682)Wtsi>/Epb41l2<Gt(AL0682)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	21482674
MGI:5056430	M	MP:0001925	male infertility	Epb41l2<Gt(AL0682)Wtsi>/Epb41l2<Gt(AL0682)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	21482674
MGI:5056430	M	MP:0004852	decreased testis weight	Epb41l2<Gt(AL0682)Wtsi>/Epb41l2<Gt(AL0682)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	21482674
MGI:5056430	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Epb41l2<Gt(AL0682)Wtsi>/Epb41l2<Gt(AL0682)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	21482674
MGI:5056430	M	MP:0002687	oligozoospermia	Epb41l2<Gt(AL0682)Wtsi>/Epb41l2<Gt(AL0682)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	21482674
MGI:5056430	M	MP:0001156	abnormal spermatogenesis	Epb41l2<Gt(AL0682)Wtsi>/Epb41l2<Gt(AL0682)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	21482674
MGI:5056442	M	MP:0002687	oligozoospermia	Aurkb<tm1.2Mama>/Aurkb<+>	involves: 129/Sv * BALB/cJ * C57BL/6 * CD-1 * SJL	N	21613325
MGI:5085904	M	MP:0009647	decreased fertilization frequency	Sec23ip<tm1.1Katn>/Sec23ip<tm1.1Katn>	involves: C57BL/6 * CBA	N	21640725
MGI:5085904	M	MP:0002686	globozoospermia	Sec23ip<tm1.1Katn>/Sec23ip<tm1.1Katn>	involves: C57BL/6 * CBA	N	21640725
MGI:5085904	M	MP:0006380	abnormal spermatid morphology	Sec23ip<tm1.1Katn>/Sec23ip<tm1.1Katn>	involves: C57BL/6 * CBA	N	21640725
MGI:5085904	M	MP:0009232	abnormal sperm nucleus morphology	Sec23ip<tm1.1Katn>/Sec23ip<tm1.1Katn>	involves: C57BL/6 * CBA	N	21640725
MGI:5085904	M	MP:0031354	abnormal acrosome assembly	Sec23ip<tm1.1Katn>/Sec23ip<tm1.1Katn>	involves: C57BL/6 * CBA	N	21640725
MGI:5085904	M	MP:0001922	reduced male fertility	Sec23ip<tm1.1Katn>/Sec23ip<tm1.1Katn>	involves: C57BL/6 * CBA	N	21640725
MGI:5085904	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Sec23ip<tm1.1Katn>/Sec23ip<tm1.1Katn>	involves: C57BL/6 * CBA	N	21640725
MGI:5085904	M	MP:0001932	abnormal spermiogenesis	Sec23ip<tm1.1Katn>/Sec23ip<tm1.1Katn>	involves: C57BL/6 * CBA	N	21640725
MGI:5086005	M	MP:0002896	abnormal bone mineralization	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0005108	abnormal ulna morphology	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0000074	abnormal neurocranium morphology	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0010025	decreased total body fat amount	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0009432	increased fetal weight	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0003723	abnormal long bone morphology	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0005422	osteosclerosis	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0000441	increased cranium width	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0000439	enlarged cranium	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0001575	cyanosis	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0001780	decreased brown adipose tissue amount	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0011386	increased metanephric mesenchyme apoptosis	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0003827	abnormal Wolffian duct morphology	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0004353	abnormal deltoid tuberosity morphology	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0000274	enlarged heart	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0002135	abnormal kidney morphology	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0006032	abnormal ureteric bud morphology	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0002833	increased heart weight	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0010984	abnormal metanephric mesenchyme morphology	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0004199	increased fetal size	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0004354	absent deltoid tuberosity	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0000527	abnormal kidney development	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0000520	absent kidney	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0030316	enlarged neurocranium	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0000694	spleen hypoplasia	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0001783	decreased white adipose tissue amount	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0003797	abnormal compact bone morphology	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0004361	bowed ulna	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0000157	abnormal sternum morphology	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0030885	increased radius size	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0011087	neonatal lethality, complete penetrance	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0003604	single kidney	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0003419	delayed endochondral bone ossification	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0003420	delayed intramembranous bone ossification	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0008277	abnormal sternum ossification	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0008273	abnormal intramembranous bone ossification	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0004374	bowed radius	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0005508	abnormal skeleton morphology	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0002835	abnormal cranial suture morphology	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0008272	abnormal endochondral bone ossification	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086005	M	MP:0003068	enlarged kidney	Amer1<tm1.2Nbar>/Y	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086006	F	MP:0004199	increased fetal size	Amer1<tm1.2Nbar>/Amer1<+>	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086006	F	MP:0009432	increased fetal weight	Amer1<tm1.2Nbar>/Amer1<+>	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086006	F	MP:0000062	increased bone mineral density	Amer1<tm1.2Nbar>/Amer1<+>	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086009	M	MP:0009250	abnormal appendicular skeleton morphology	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0003723	abnormal long bone morphology	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0003797	abnormal compact bone morphology	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0005422	osteosclerosis	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0008395	abnormal osteoblast differentiation	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0010875	increased bone volume	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0011168	abnormal fat cell differentiation	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0020080	increased bone mineralization	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0004988	increased osteoblast cell number	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0020039	increased bone ossification	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0009347	increased trabecular bone thickness	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0009115	abnormal fat cell morphology	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0008277	abnormal sternum ossification	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0003795	abnormal bone structure	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0004353	abnormal deltoid tuberosity morphology	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0000157	abnormal sternum morphology	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0020138	delayed bone mineralization	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086009	M	MP:0000130	abnormal trabecular bone morphology	Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	21571217
MGI:5086010	M	MP:0005390	skeleton phenotype	Amer1<tm1.1Nbar>/Y,Tg(Col2a1-cre)1Bhr/0	involves: 129S4/SvJae * C57BL/6 * SJL	Y	21571217
MGI:5086011	M	MP:0005390	skeleton phenotype	Amer1<tm1.1Nbar>/Y,Tg(BGLAP-cre)1Clem/0	involves: 129S4/SvJae * C57BL/6 * FVB/NJ * SJL	Y	21571217
MGI:5086012	M	MP:0009347	increased trabecular bone thickness	Amer1<tm1.1Nbar>/Y,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086012	M	MP:0020080	increased bone mineralization	Amer1<tm1.1Nbar>/Y,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086012	M	MP:0020039	increased bone ossification	Amer1<tm1.1Nbar>/Y,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086012	M	MP:0004988	increased osteoblast cell number	Amer1<tm1.1Nbar>/Y,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086012	M	MP:0030393	delayed fontanelle closure	Amer1<tm1.1Nbar>/Y,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086012	M	MP:0002113	abnormal skeleton development	Amer1<tm1.1Nbar>/Y,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086012	M	MP:0010875	increased bone volume	Amer1<tm1.1Nbar>/Y,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086012	M	MP:0003795	abnormal bone structure	Amer1<tm1.1Nbar>/Y,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086012	M	MP:0005422	osteosclerosis	Amer1<tm1.1Nbar>/Y,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0	involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	N	21571217
MGI:5086015	M	MP:0005390	skeleton phenotype	Ctnnb1<tm2Kem>/Ctnnb1<+>,Amer1<tm1.1Nbar>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129 * C57BL/6 * SJL	Y	21571217
MGI:5086118	F	MP:0002020	increased tumor incidence	Amelx<tm1Kul>/Amelx<tm1Kul>,Tg(AMELX*P70T)2Gibs/?	involves: 129S1/Sv * 129X1/SvJ	N	17384027
MGI:5086118	F	MP:0002576	abnormal enamel morphology	Amelx<tm1Kul>/Amelx<tm1Kul>,Tg(AMELX*P70T)2Gibs/?	involves: 129S1/Sv * 129X1/SvJ	N	17384027
MGI:5086213	M	MP:0001154	seminiferous tubule degeneration	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	F	MP:0001127	small ovary	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	F	MP:0008871	abnormal ovarian follicle number	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	F	MP:0003699	abnormal female reproductive system physiology	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	F	MP:0002016	ovary cyst	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0006378	abnormal spermatogonia morphology	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0005159	azoospermia	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0002216	abnormal seminiferous tubule morphology	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0001925	male infertility	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0006362	abnormal male germ cell morphology	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0001153	small seminiferous tubules	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0001147	small testis	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0004901	decreased male germ cell number	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0005169	abnormal male meiosis	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	F	MP:0001926	female infertility	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0002685	abnormal spermatogonia proliferation	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0006380	abnormal spermatid morphology	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	F	MP:0005431	decreased oocyte number	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	F	MP:0011125	decreased primary ovarian follicle number	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0014052	increased male germ cell apoptosis	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0008261	arrest of male meiosis	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086213	M	MP:0006379	abnormal spermatocyte morphology	Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>	B6.129P2-Ranbp9<Gt(RHA056)Byg>	N	21561988
MGI:5086218	F	MP:0002577	reduced enamel thickness	Amelx<tm1Kul>/Amelx<tm1Kul>,Tg(AMELX-LRAP)9Gibs/0	involves: 129S1/Sv * 129X1/SvJ	N	12958690
MGI:5086218	F	MP:0002649	abnormal enamel rod pattern	Amelx<tm1Kul>/Amelx<tm1Kul>,Tg(AMELX-LRAP)9Gibs/0	involves: 129S1/Sv * 129X1/SvJ	N	12958690
MGI:5086218	F	MP:0002576	abnormal enamel morphology	Amelx<tm1Kul>/Amelx<tm1Kul>,Tg(AMELX-LRAP)9Gibs/0	involves: 129S1/Sv * 129X1/SvJ	N	12958690
MGI:5086221	M	MP:0001529	abnormal vocalization	Shank3<tm1.1Pfw>/Shank3<+>	B6.129S6-Shank3<tm1.1Pfw>	N	MGI:5499103
MGI:5086228	M	MP:0001922	reduced male fertility	Glrb<spa>/Glrb<spa>,Tg(Eno2-Glrb)456Wha/0	involves: C3HeB/FeLe * C57BL/6 * C57BL/6J * DBA/2	N	10651857
MGI:5086229	M	MP:0001922	reduced male fertility	Glrb<spa>/Glrb<spa>	involves: C3HeB/FeLe * C57BL/6 * C57BL/6J * DBA/2	N	10651857
MGI:5140119	M	MP:0001393	ataxia	Gjb1<tm1Kwi>/Y,Gjc2<tm2.1Kwi>/Gjc2<tm2.1Kwi>	involves: 129S4/SvJae * C57BL/6 * SJL	N	21750683
MGI:5140119	M	MP:0000920	abnormal myelination	Gjb1<tm1Kwi>/Y,Gjc2<tm2.1Kwi>/Gjc2<tm2.1Kwi>	involves: 129S4/SvJae * C57BL/6 * SJL	N	21750683
MGI:5140119	M	MP:0002083	premature death	Gjb1<tm1Kwi>/Y,Gjc2<tm2.1Kwi>/Gjc2<tm2.1Kwi>	involves: 129S4/SvJae * C57BL/6 * SJL	N	21750683
MGI:5140119	M	MP:0003354	astrocytosis	Gjb1<tm1Kwi>/Y,Gjc2<tm2.1Kwi>/Gjc2<tm2.1Kwi>	involves: 129S4/SvJae * C57BL/6 * SJL	N	21750683
MGI:5140119	M	MP:0002066	abnormal motor capabilities/coordination/movement	Gjb1<tm1Kwi>/Y,Gjc2<tm2.1Kwi>/Gjc2<tm2.1Kwi>	involves: 129S4/SvJae * C57BL/6 * SJL	N	21750683
MGI:5140195	M	MP:0011100	preweaning lethality, complete penetrance	Nano/Y	involves: BALB/cAnNCrl * C3H/HeNCrl	N	10932191
MGI:5140204	M	MP:0001925	male infertility	Jam3<tm1.2Chav>/Jam3<tm1.2Chav>	involves: 129 * C57BL/6	N	21593193
MGI:5140205	M	MP:0001925	male infertility	Jam3<tm1.2Chav>/Jam3<tm1.2Chav>	B6.129-Jam3<tm1.2Chav>	N	21593193
MGI:5140348	M	MP:0008261	arrest of male meiosis	Tex19.1<tm1(rtTA2S*M2,lacZ)Jw>/Tex19.1<tm1(rtTA2S*M2,lacZ)Jw>	involves: 129S4/SvJae * C57BL/6	N	21103378
MGI:5140348	M	MP:0001147	small testis	Tex19.1<tm1(rtTA2S*M2,lacZ)Jw>/Tex19.1<tm1(rtTA2S*M2,lacZ)Jw>	involves: 129S4/SvJae * C57BL/6	N	21103378
MGI:5140853	M	MP:0001922	reduced male fertility	Vasn<tm1Zgl>/Vasn<tm1Zgl>	B6.Cg-Vasn<tm1Zgl>	N	21658601
MGI:5140853	M	MP:0008280	abnormal male germ cell apoptosis	Vasn<tm1Zgl>/Vasn<tm1Zgl>	B6.Cg-Vasn<tm1Zgl>	N	21658601
MGI:5140950	F	MP:0001386	abnormal maternal nurturing	Cdh23<v-bus>/Cdh23<v-bus>	involves: KYF/MsIdr	N	MGI:61189
MGI:5140970	F	MP:0010768	mortality/aging	Tlr7<tm1Aki>/Tlr7<tm1Aki>,Unc93b1<tm1.1Kmiy>/Unc93b1<tm1.1Kmiy>	involves: 129P2/OlaHsd * C57BL/6	Y	21683627
MGI:5140970	F	MP:0005397	hematopoietic system phenotype	Tlr7<tm1Aki>/Tlr7<tm1Aki>,Unc93b1<tm1.1Kmiy>/Unc93b1<tm1.1Kmiy>	involves: 129P2/OlaHsd * C57BL/6	Y	21683627
MGI:5141129	M	MP:0004045	abnormal cell cycle checkpoint function	Tspyl2<tm1Sich>/Y	involves: 129S/SvEv	N	21738728
MGI:5141129	M	MP:0005384	cellular phenotype	Tspyl2<tm1Sich>/Y	involves: 129S/SvEv	Y	21738728
MGI:5141129	M	MP:0002006	neoplasm	Tspyl2<tm1Sich>/Y	involves: 129S/SvEv	Y	21738728
MGI:5141129	M	MP:0003631	nervous system phenotype	Tspyl2<tm1Sich>/Y	involves: 129S/SvEv	Y	21738728
MGI:5141129	M	MP:0005389	reproductive system phenotype	Tspyl2<tm1Sich>/Y	involves: 129S/SvEv	Y	21738728
MGI:5141129	M	MP:0010768	mortality/aging	Tspyl2<tm1Sich>/Y	involves: 129S/SvEv	Y	21738728
MGI:5141130	F	MP:0003631	nervous system phenotype	Tspyl2<tm1Sich>/Tspyl2<tm1Sich>	involves: 129S/SvEv	Y	21738728
MGI:5141130	F	MP:0005384	cellular phenotype	Tspyl2<tm1Sich>/Tspyl2<tm1Sich>	involves: 129S/SvEv	Y	21738728
MGI:5141130	F	MP:0004045	abnormal cell cycle checkpoint function	Tspyl2<tm1Sich>/Tspyl2<tm1Sich>	involves: 129S/SvEv	N	21738728
MGI:5141130	F	MP:0005389	reproductive system phenotype	Tspyl2<tm1Sich>/Tspyl2<tm1Sich>	involves: 129S/SvEv	Y	21738728
MGI:5141130	F	MP:0010768	mortality/aging	Tspyl2<tm1Sich>/Tspyl2<tm1Sich>	involves: 129S/SvEv	Y	21738728
MGI:5141130	F	MP:0002006	neoplasm	Tspyl2<tm1Sich>/Tspyl2<tm1Sich>	involves: 129S/SvEv	Y	21738728
MGI:5141275	M	MP:0002780	decreased circulating testosterone level	Gata4<tm1.1Jmol>/Gata4<tm1.1Jmol>	involves: 129 * C57BL/6	N	30793514
MGI:5141275	M	MP:0004910	decreased seminal vesicle weight	Gata4<tm1.1Jmol>/Gata4<tm1.1Jmol>	involves: 129 * C57BL/6	N	30793514
MGI:5141497	F	MP:0009082	uterus cyst	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	21467199
MGI:5141497	F	MP:0009671	abnormal uterus physiology	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	21467199
MGI:5141497	F	MP:0013401	increased endometrial gland number	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	21467199
MGI:5141497	F	MP:0002016	ovary cyst	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	21467199
MGI:5141497	F	MP:0009251	enlarged endometrial glands	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>	involves: 129S7/SvEvBrd * C57BL/6J	N	21467199
MGI:5141498	F	MP:0009082	uterus cyst	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>,crsp/crsp	involves: 129S7/SvEvBrd * C57BL/6J * FVB	N	21467199
MGI:5141498	F	MP:0009251	enlarged endometrial glands	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>,crsp/crsp	involves: 129S7/SvEvBrd * C57BL/6J * FVB	N	21467199
MGI:5141498	F	MP:0013401	increased endometrial gland number	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>,crsp/crsp	involves: 129S7/SvEvBrd * C57BL/6J * FVB	N	21467199
MGI:5141498	F	MP:0002016	ovary cyst	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>,crsp/crsp	involves: 129S7/SvEvBrd * C57BL/6J * FVB	N	21467199
MGI:5141500	F	MP:0009251	enlarged endometrial glands	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>,crsp/+	involves: 129S7/SvEvBrd * C57BL/6J * FVB	N	21467199
MGI:5141500	F	MP:0009082	uterus cyst	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>,crsp/+	involves: 129S7/SvEvBrd * C57BL/6J * FVB	N	21467199
MGI:5141500	F	MP:0002016	ovary cyst	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>,crsp/+	involves: 129S7/SvEvBrd * C57BL/6J * FVB	N	21467199
MGI:5141500	F	MP:0013401	increased endometrial gland number	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>,crsp/+	involves: 129S7/SvEvBrd * C57BL/6J * FVB	N	21467199
MGI:5141501	F	MP:0009671	abnormal uterus physiology	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>,Rxfp2<tm1Aia>/Rxfp2<+>	involves: 129S7/SvEvBrd * C57BL/6J * FVB	N	21467199
MGI:5141501	F	MP:0002016	ovary cyst	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>,Rxfp2<tm1Aia>/Rxfp2<+>	involves: 129S7/SvEvBrd * C57BL/6J * FVB	N	21467199
MGI:5141501	F	MP:0009082	uterus cyst	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>,Rxfp2<tm1Aia>/Rxfp2<+>	involves: 129S7/SvEvBrd * C57BL/6J * FVB	N	21467199
MGI:5141501	F	MP:0013401	increased endometrial gland number	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>,Rxfp2<tm1Aia>/Rxfp2<+>	involves: 129S7/SvEvBrd * C57BL/6J * FVB	N	21467199
MGI:5141501	F	MP:0009251	enlarged endometrial glands	Cav1<tm1.1Aia>/Cav1<tm1.1Aia>,Rxfp2<tm1Aia>/Rxfp2<+>	involves: 129S7/SvEvBrd * C57BL/6J * FVB	N	21467199
MGI:5141626	M	MP:0003698	abnormal male reproductive system physiology	Tg(H2-K1-Ifnb1)10Seif/Tg(H2-K1-Ifnb1)10Seif	C3H/HeOuJ-Tg(H2-K1-Ifnb1)10Seif	N	21515676
MGI:5141626	M	MP:0001922	reduced male fertility	Tg(H2-K1-Ifnb1)10Seif/Tg(H2-K1-Ifnb1)10Seif	C3H/HeOuJ-Tg(H2-K1-Ifnb1)10Seif	N	21515676
MGI:5141626	M	MP:0001146	abnormal testis morphology	Tg(H2-K1-Ifnb1)10Seif/Tg(H2-K1-Ifnb1)10Seif	C3H/HeOuJ-Tg(H2-K1-Ifnb1)10Seif	N	21515676
MGI:5141626	M	MP:0001154	seminiferous tubule degeneration	Tg(H2-K1-Ifnb1)10Seif/Tg(H2-K1-Ifnb1)10Seif	C3H/HeOuJ-Tg(H2-K1-Ifnb1)10Seif	N	21515676
MGI:5141626	M	MP:0008280	abnormal male germ cell apoptosis	Tg(H2-K1-Ifnb1)10Seif/Tg(H2-K1-Ifnb1)10Seif	C3H/HeOuJ-Tg(H2-K1-Ifnb1)10Seif	N	21515676
MGI:5141626	M	MP:0001932	abnormal spermiogenesis	Tg(H2-K1-Ifnb1)10Seif/Tg(H2-K1-Ifnb1)10Seif	C3H/HeOuJ-Tg(H2-K1-Ifnb1)10Seif	N	21515676
MGI:5141626	M	MP:0002216	abnormal seminiferous tubule morphology	Tg(H2-K1-Ifnb1)10Seif/Tg(H2-K1-Ifnb1)10Seif	C3H/HeOuJ-Tg(H2-K1-Ifnb1)10Seif	N	21515676
MGI:5141626	M	MP:0004852	decreased testis weight	Tg(H2-K1-Ifnb1)10Seif/Tg(H2-K1-Ifnb1)10Seif	C3H/HeOuJ-Tg(H2-K1-Ifnb1)10Seif	N	21515676
MGI:5141626	M	MP:0001925	male infertility	Tg(H2-K1-Ifnb1)10Seif/Tg(H2-K1-Ifnb1)10Seif	C3H/HeOuJ-Tg(H2-K1-Ifnb1)10Seif	N	21515676
MGI:5141626	M	MP:0002687	oligozoospermia	Tg(H2-K1-Ifnb1)10Seif/Tg(H2-K1-Ifnb1)10Seif	C3H/HeOuJ-Tg(H2-K1-Ifnb1)10Seif	N	21515676
MGI:5142270	M	MP:0002051	increased skin papilloma incidence	Egfr<wa2>/Egfr<+>,Rps6ka3<tm1.1Kry>/Y,Tg(KRT5-SOS1)892A6Wag/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	21119595
MGI:5142270	M	MP:0003447	decreased tumor growth/size	Egfr<wa2>/Egfr<+>,Rps6ka3<tm1.1Kry>/Y,Tg(KRT5-SOS1)892A6Wag/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	21119595
MGI:5142491	F	MP:0001923	reduced female fertility	Kitl<Sl-m>/Kitl<Sl-m>	involves: C57BL/6	N	MGI:61609
MGI:5142491	F	MP:0001923	reduced female fertility	Kitl<Sl-m>/Kitl<Sl-m>	involves: C57BL/6	N	MGI:61345
MGI:5142491	M	MP:0001925	male infertility	Kitl<Sl-m>/Kitl<Sl-m>	involves: C57BL/6	N	MGI:61609
MGI:5142524	F	MP:0001144	vagina atresia	Kitl<Sl-Clo>/Kitl<Sl-Clo>	Not Specified	N	MGI:61836
MGI:5284727	M	MP:0001925	male infertility	hml/hml	CByJ.Cg-hml/J	N	21179397
MGI:5284727	F	MP:0001926	female infertility	hml/hml	CByJ.Cg-hml/J	N	21179397
MGI:5284893	F	MP:0005240	abnormal amacrine cell morphology	Plxna1<tm1Tmj>/Plxna1<tm1Tmj>,Plxna3<tm1Matl>/Plxna3<tm1Matl>	involves: 129S/SvEv * 129S1/Sv	N	21835343
MGI:5284893	F	MP:0006073	abnormal retina bipolar cell morphology	Plxna1<tm1Tmj>/Plxna1<tm1Tmj>,Plxna3<tm1Matl>/Plxna3<tm1Matl>	involves: 129S/SvEv * 129S1/Sv	N	21835343
MGI:5284893	F	MP:0003733	abnormal retina inner nuclear layer morphology	Plxna1<tm1Tmj>/Plxna1<tm1Tmj>,Plxna3<tm1Matl>/Plxna3<tm1Matl>	involves: 129S/SvEv * 129S1/Sv	N	21835343
MGI:5284893	F	MP:0008415	abnormal neurite morphology	Plxna1<tm1Tmj>/Plxna1<tm1Tmj>,Plxna3<tm1Matl>/Plxna3<tm1Matl>	involves: 129S/SvEv * 129S1/Sv	N	21835343
MGI:5284893	F	MP:0003734	abnormal retina inner plexiform layer morphology	Plxna1<tm1Tmj>/Plxna1<tm1Tmj>,Plxna3<tm1Matl>/Plxna3<tm1Matl>	involves: 129S/SvEv * 129S1/Sv	N	21835343
MGI:5284893	F	MP:0008056	abnormal retina ganglion cell morphology	Plxna1<tm1Tmj>/Plxna1<tm1Tmj>,Plxna3<tm1Matl>/Plxna3<tm1Matl>	involves: 129S/SvEv * 129S1/Sv	N	21835343
MGI:5284893	F	MP:0003732	abnormal retina outer plexiform layer morphology	Plxna1<tm1Tmj>/Plxna1<tm1Tmj>,Plxna3<tm1Matl>/Plxna3<tm1Matl>	involves: 129S/SvEv * 129S1/Sv	N	21835343
MGI:5285095	F	MP:0005168	abnormal female meiosis	Hsf1<tm1Ijb>/Hsf1<tm1Ijb>	involves: 129S6/SvEvTac	N	21690297
MGI:5285188	F	MP:0005168	abnormal female meiosis	Hsf1<tm1.1Echr>/Hsf1<tm1.1Echr>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	21690297
MGI:5285205	F	MP:0009097	absent endometrial glands	Wnt7a<tm1.1Tesp>/Wnt7a<tm1.1Tesp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * SJL	N	21508348
MGI:5285205	F	MP:0001926	female infertility	Wnt7a<tm1.1Tesp>/Wnt7a<tm1.1Tesp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * SJL	N	21508348
MGI:5285205	F	MP:0009669	abnormal postimplantation uterine environment	Wnt7a<tm1.1Tesp>/Wnt7a<tm1.1Tesp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * SJL	N	21508348
MGI:5285429	F	MP:0011121	decreased primordial ovarian follicle number	Mirc5<tm1Jae>/Mirc5<tm1Jae>	involves: 129S4/SvJae * C57BL/6	N	21844366
MGI:5285429	M	MP:0002216	abnormal seminiferous tubule morphology	Mirc5<tm1Jae>/Mirc5<tm1Jae>	involves: 129S4/SvJae * C57BL/6	N	21844366
MGI:5285429	M	MP:0004901	decreased male germ cell number	Mirc5<tm1Jae>/Mirc5<tm1Jae>	involves: 129S4/SvJae * C57BL/6	N	21844366
MGI:5285429	F	MP:0008871	abnormal ovarian follicle number	Mirc5<tm1Jae>/Mirc5<tm1Jae>	involves: 129S4/SvJae * C57BL/6	N	21844366
MGI:5285429	F	MP:0001127	small ovary	Mirc5<tm1Jae>/Mirc5<tm1Jae>	involves: 129S4/SvJae * C57BL/6	N	21844366
MGI:5285429	F	MP:0001926	female infertility	Mirc5<tm1Jae>/Mirc5<tm1Jae>	involves: 129S4/SvJae * C57BL/6	N	21844366
MGI:5285429	F	MP:0005431	decreased oocyte number	Mirc5<tm1Jae>/Mirc5<tm1Jae>	involves: 129S4/SvJae * C57BL/6	N	21844366
MGI:5285429	F	MP:0002777	absent ovarian follicles	Mirc5<tm1Jae>/Mirc5<tm1Jae>	involves: 129S4/SvJae * C57BL/6	N	21844366
MGI:5285451	M	MP:0001970	abnormal pain threshold	Adamts5<tm2.2Lex>/Adamts5<tm2.2Lex>	B6.129S5-Adamts5<tm2.2Lex>	N	20036347
MGI:5285687	F	MP:0005387	immune system phenotype	Rbm3<tm1Ttg>/Rbm3<tm1Ttg>	involves: 129P2/OlaHsd	Y	21684257
MGI:5285687	F	MP:0011704	decreased fibroblast proliferation	Rbm3<tm1Ttg>/Rbm3<tm1Ttg>	involves: 129P2/OlaHsd	N	21684257
MGI:5285687	F	MP:0003077	abnormal cell cycle	Rbm3<tm1Ttg>/Rbm3<tm1Ttg>	involves: 129P2/OlaHsd	N	21684257
MGI:5285846	F	MP:0002169	no abnormal phenotype detected	Tsix<tm1.1Awu>/Tsix<tm1.1Awu>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285847	M	MP:0002169	no abnormal phenotype detected	Tsix<tm1.1Awu>/Y,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285848	F	MP:0003787	abnormal imprinting	Tsix<tm1.1Awu>/Tsix<+>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285848	F	MP:0003984	embryonic growth retardation	Tsix<tm1.1Awu>/Tsix<+>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285848	F	MP:0003658	abnormal capillary morphology	Tsix<tm1.1Awu>/Tsix<+>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285848	F	MP:0004259	small placenta	Tsix<tm1.1Awu>/Tsix<+>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285848	F	MP:0008877	abnormal DNA methylation	Tsix<tm1.1Awu>/Tsix<+>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285848	F	MP:0020329	decreased capillary density	Tsix<tm1.1Awu>/Tsix<+>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285848	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Tsix<tm1.1Awu>/Tsix<+>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285848	F	MP:0001716	abnormal placenta labyrinth morphology	Tsix<tm1.1Awu>/Tsix<+>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285848	F	MP:0005033	abnormal trophoblast giant cell morphology	Tsix<tm1.1Awu>/Tsix<+>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285848	F	MP:0009397	increased trophoblast giant cell number	Tsix<tm1.1Awu>/Tsix<+>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285848	F	MP:0012100	absent spongiotrophoblast	Tsix<tm1.1Awu>/Tsix<+>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285848	F	MP:0005031	abnormal trophoblast layer morphology	Tsix<tm1.1Awu>/Tsix<+>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285848	F	MP:0003403	absent placental labyrinth	Tsix<tm1.1Awu>/Tsix<+>,Tg(CAG-EGFP)50Osb/0,Gt(ROSA)26Sor<tm1(rtTA)Awu>/Gt(ROSA)26Sor<tm1(rtTA)Awu>	involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc	N	21852535
MGI:5285948	F	MP:0004047	abnormal milk composition	Csn1s1<tm1Afk>/Csn1s1<tm1Afk>	involves: 129 * C57BL/6	N	21789179
MGI:5285948	F	MP:0013716	hypolactation	Csn1s1<tm1Afk>/Csn1s1<tm1Afk>	involves: 129 * C57BL/6	N	21789179
MGI:5285948	F	MP:0020880	abnormal milk calcium level	Csn1s1<tm1Afk>/Csn1s1<tm1Afk>	involves: 129 * C57BL/6	N	21789179
MGI:5285948	F	MP:0020886	abnormal milk phosphate level	Csn1s1<tm1Afk>/Csn1s1<tm1Afk>	involves: 129 * C57BL/6	N	21789179
MGI:5285949	F	MP:0004047	abnormal milk composition	Csn1s1<tm1Afk>/Csn1s1<+>	involves: 129 * C57BL/6	N	21789179
MGI:5286088	M	MP:0001158	abnormal prostate gland morphology	Akap12<tm1Ihg>/Akap12<tm1Ihg>	involves: 129S4/SvJae * C57BL/6	N	18593908
MGI:5286088	M	MP:0031365	prostate gland ventral lobe hyperplasia	Akap12<tm1Ihg>/Akap12<tm1Ihg>	involves: 129S4/SvJae * C57BL/6	N	18593908
MGI:5286088	M	MP:0003607	abnormal prostate gland physiology	Akap12<tm1Ihg>/Akap12<tm1Ihg>	involves: 129S4/SvJae * C57BL/6	N	18593908
MGI:5286088	M	MP:0005305	prostate gland anterior lobe hyperplasia	Akap12<tm1Ihg>/Akap12<tm1Ihg>	involves: 129S4/SvJae * C57BL/6	N	18593908
MGI:5286088	M	MP:0004961	increased prostate gland weight	Akap12<tm1Ihg>/Akap12<tm1Ihg>	involves: 129S4/SvJae * C57BL/6	N	18593908
MGI:5286587	M	MP:0002687	oligozoospermia	Qki<qk-v>/Qki<qk-v>,Tg(PGK2-Pacrg)#Jus/?	involves: BTBR * C57BL/6J * DBA/2	N	15148410
MGI:5287996	F	MP:0001923	reduced female fertility	Atad2b<Tg(Tyr)2295B-4Ove>/Atad2b<Tg(Tyr)2295B-4Ove>	FVB/N-Atad2b<Tg(Tyr)2295B-4Ove>	N	MGI:5286747
MGI:5288006	F	MP:0001126	abnormal ovary morphology	Notch2<tm3Grid>/Notch2<tm3Grid>,Tg(Tpbpa-cre,-EGFP)5Jcc/0	involves: 129S1/Sv	N	21693515
MGI:5288006	F	MP:0009444	ovarian follicular cyst	Notch2<tm3Grid>/Notch2<tm3Grid>,Tg(Tpbpa-cre,-EGFP)5Jcc/0	involves: 129S1/Sv	N	21693515
MGI:5288006	F	MP:0004834	ovary hemorrhage	Notch2<tm3Grid>/Notch2<tm3Grid>,Tg(Tpbpa-cre,-EGFP)5Jcc/0	involves: 129S1/Sv	N	21693515
MGI:5288006	F	MP:0009661	abnormal pregnancy	Notch2<tm3Grid>/Notch2<tm3Grid>,Tg(Tpbpa-cre,-EGFP)5Jcc/0	involves: 129S1/Sv	N	21693515
MGI:5288056	F	MP:0001926	female infertility	Cks2<TgTn(sb-cHS4,Tyr)2525F-2Ove>/Cks2<TgTn(sb-cHS4,Tyr)2525F-2Ove>	FVB/N-Cks2<TgTn(sb-cHS4,Tyr)2525F-2Ove>	N	MGI:5286747
MGI:5288057	M	MP:0001925	male infertility	Cnpy4<Tg(Tyr)2356C-2a1Ove>/Cnpy4<Tg(Tyr)2356C-2a1Ove>	FVB/N-Cnpy4<Tg(Tyr)2356C-2a1Ove>	N	MGI:5286747
MGI:5288061	M	MP:0001925	male infertility	Fam91a1<Tg(Tyr)2261COve>/Fam91a1<Tg(Tyr)2261COve>	FVB/N-Fam91a1<Tg(Tyr)2261COve>	N	MGI:5286747
MGI:5288062	M	MP:0001925	male infertility	Dgka<TgTn(sb-cHS4,Tyr)2320A-2Ove>/Dgka<TgTn(sb-cHS4,Tyr)2320A-2Ove>	FVB/N-Dgka<TgTn(sb-cHS4,Tyr)2320A-2Ove>	N	MGI:5286747
MGI:5288071	M	MP:0001925	male infertility	Hsp90aa1<Tg(Tyr)2396BOve>/Hsp90aa1<Tg(Tyr)2396BOve>	FVB/N-Hsp90aa1<Tg(Tyr)2396BOve>	N	MGI:5286747
MGI:5288071	M	MP:0001147	small testis	Hsp90aa1<Tg(Tyr)2396BOve>/Hsp90aa1<Tg(Tyr)2396BOve>	FVB/N-Hsp90aa1<Tg(Tyr)2396BOve>	N	MGI:5286747
MGI:5288148	F	MP:0001127	small ovary	Midn<Tg(Tyr)2261EOve>/Midn<Tg(Tyr)2261EOve>	FVB/N-Midn<Tg(Tyr)2261EOve>	N	MGI:5286747
MGI:5288184	M	MP:0001925	male infertility	Rnf41<TgTn(sb-rtTA,Tyr)2435COve>/Rnf41<TgTn(sb-rtTA,Tyr)2435COve>	involves: C57BL/6 * FVB/N	N	MGI:5286747
MGI:5288193	M	MP:0005159	azoospermia	Stag3<TgTn(sb-cHS4,Tyr)2312COve>/Stag3<TgTn(sb-cHS4,Tyr)2312COve>	FVB/N-Stag3<TgTn(sb-cHS4,Tyr)2312COve>	N	MGI:5286747
MGI:5288193	F	MP:0004805	absent oocytes	Stag3<TgTn(sb-cHS4,Tyr)2312COve>/Stag3<TgTn(sb-cHS4,Tyr)2312COve>	FVB/N-Stag3<TgTn(sb-cHS4,Tyr)2312COve>	N	MGI:5286747
MGI:5288199	F	MP:0001923	reduced female fertility	Ubap2l<TgTn(sb-cHS4,Tyr)2326F-3b2Ove>/Ubap2l<TgTn(sb-cHS4,Tyr)2326F-3b2Ove>	FVB/N-Ubap2l<TgTn(sb-cHS4,Tyr)2326F-3b2Ove>	N	MGI:5286747
MGI:5288237	M	MP:0011290	decreased nephron number	Gdnf<tm1Lmgd>/Gdnf<+>	B6.129-Gdnf<tm1Lmgd>	N	12574104
MGI:5288374	F	MP:0001926	female infertility	In(10C1;Ccdc53)4Ove/In(10C1;Ccdc53)4Ove	involves: FVB/N	N	MGI:5286747
MGI:5288400	F	MP:0009659	striated fur	Ta33Hl/Ta33Hl<+>	involves: BALB/c * C3H/HeH	N	MGI:4940633
MGI:5288408	F	MP:0005382	craniofacial phenotype	Ta33Hl/Ta33Hl	involves: BALB/c * C3H/HeH	Y	MGI:4940633
MGI:5288408	F	MP:0006365	absent guard hair	Ta33Hl/Ta33Hl	involves: BALB/c * C3H/HeH	N	MGI:4940633
MGI:5288408	F	MP:0000418	focal hair loss	Ta33Hl/Ta33Hl	involves: BALB/c * C3H/HeH	N	MGI:4940633
MGI:5288411	M	MP:0006365	absent guard hair	Ta33Hl/Y	involves: BALB/c * C3H/HeH	N	MGI:4940633
MGI:5288411	M	MP:0005382	craniofacial phenotype	Ta33Hl/Y	involves: BALB/c * C3H/HeH	Y	MGI:4940633
MGI:5288411	M	MP:0000418	focal hair loss	Ta33Hl/Y	involves: BALB/c * C3H/HeH	N	MGI:4940633
MGI:5289962	M	MP:0009230	abnormal sperm head morphology	Zfp42<tm1.1Log>/Zfp42<tm1.1Log>	involves: 129S1/Sv * C57BL/6 * C57BL/6J	N	21641340
MGI:5289962	M	MP:0004901	decreased male germ cell number	Zfp42<tm1.1Log>/Zfp42<tm1.1Log>	involves: 129S1/Sv * C57BL/6 * C57BL/6J	N	21641340
MGI:5289962	M	MP:0009237	kinked sperm flagellum	Zfp42<tm1.1Log>/Zfp42<tm1.1Log>	involves: 129S1/Sv * C57BL/6 * C57BL/6J	N	21641340
MGI:5289962	M	MP:0002687	oligozoospermia	Zfp42<tm1.1Log>/Zfp42<tm1.1Log>	involves: 129S1/Sv * C57BL/6 * C57BL/6J	N	21641340
MGI:5289962	M	MP:0003205	testicular atrophy	Zfp42<tm1.1Log>/Zfp42<tm1.1Log>	involves: 129S1/Sv * C57BL/6 * C57BL/6J	N	21641340
MGI:5292056	M	MP:0009237	kinked sperm flagellum	Spink2<Gt(327A6)Cmhd>/Spink2<Gt(327A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21705336
MGI:5292056	M	MP:0002687	oligozoospermia	Spink2<Gt(327A6)Cmhd>/Spink2<Gt(327A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21705336
MGI:5292056	M	MP:0008280	abnormal male germ cell apoptosis	Spink2<Gt(327A6)Cmhd>/Spink2<Gt(327A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21705336
MGI:5292056	M	MP:0001147	small testis	Spink2<Gt(327A6)Cmhd>/Spink2<Gt(327A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21705336
MGI:5292056	M	MP:0001922	reduced male fertility	Spink2<Gt(327A6)Cmhd>/Spink2<Gt(327A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21705336
MGI:5292056	M	MP:0001153	small seminiferous tubules	Spink2<Gt(327A6)Cmhd>/Spink2<Gt(327A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21705336
MGI:5292056	M	MP:0005578	teratozoospermia	Spink2<Gt(327A6)Cmhd>/Spink2<Gt(327A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21705336
MGI:5292056	M	MP:0002216	abnormal seminiferous tubule morphology	Spink2<Gt(327A6)Cmhd>/Spink2<Gt(327A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21705336
MGI:5292056	M	MP:0004852	decreased testis weight	Spink2<Gt(327A6)Cmhd>/Spink2<Gt(327A6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21705336
MGI:5292104	F	MP:0008028	pregnancy-related premature death	Nrk<tm1Mkom>/Nrk<tm1Mkom>	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292104	F	MP:0011086	postnatal lethality, incomplete penetrance	Nrk<tm1Mkom>/Nrk<tm1Mkom>	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292104	F	MP:0012098	increased spongiotrophoblast size	Nrk<tm1Mkom>/Nrk<tm1Mkom>	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292104	F	MP:0011088	neonatal lethality, incomplete penetrance	Nrk<tm1Mkom>/Nrk<tm1Mkom>	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292104	F	MP:0004260	enlarged placenta	Nrk<tm1Mkom>/Nrk<tm1Mkom>	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292104	F	MP:0004920	increased placenta weight	Nrk<tm1Mkom>/Nrk<tm1Mkom>	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292104	F	MP:0004514	dystocia	Nrk<tm1Mkom>/Nrk<tm1Mkom>	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292105	M	MP:0004260	enlarged placenta	Nrk<tm1Mkom>/Y	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292105	M	MP:0011086	postnatal lethality, incomplete penetrance	Nrk<tm1Mkom>/Y	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292105	M	MP:0011088	neonatal lethality, incomplete penetrance	Nrk<tm1Mkom>/Y	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292105	M	MP:0004920	increased placenta weight	Nrk<tm1Mkom>/Y	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292105	M	MP:0012098	increased spongiotrophoblast size	Nrk<tm1Mkom>/Y	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292106	F	MP:0012098	increased spongiotrophoblast size	Nrk<tm1Mkom>/Nrk<+>	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292106	F	MP:0004920	increased placenta weight	Nrk<tm1Mkom>/Nrk<+>	B6.129S4-Nrk<tm1Mkom>	N	21715335
MGI:5292112	M	MP:0004852	decreased testis weight	Nrg1<tm1Sabe>/Nrg1<tm1Sabe>,Tg(Amh-cre/ERT)#Sabe/0	B6JJcl.Cg-Nrg1<tm1Sabe> Tg(Amh-cre/ERT)#Sabe	N	21715427
MGI:5292112	M	MP:0001147	small testis	Nrg1<tm1Sabe>/Nrg1<tm1Sabe>,Tg(Amh-cre/ERT)#Sabe/0	B6JJcl.Cg-Nrg1<tm1Sabe> Tg(Amh-cre/ERT)#Sabe	N	21715427
MGI:5292112	M	MP:0003698	abnormal male reproductive system physiology	Nrg1<tm1Sabe>/Nrg1<tm1Sabe>,Tg(Amh-cre/ERT)#Sabe/0	B6JJcl.Cg-Nrg1<tm1Sabe> Tg(Amh-cre/ERT)#Sabe	N	21715427
MGI:5292112	M	MP:0001156	abnormal spermatogenesis	Nrg1<tm1Sabe>/Nrg1<tm1Sabe>,Tg(Amh-cre/ERT)#Sabe/0	B6JJcl.Cg-Nrg1<tm1Sabe> Tg(Amh-cre/ERT)#Sabe	N	21715427
MGI:5292112	M	MP:0005159	azoospermia	Nrg1<tm1Sabe>/Nrg1<tm1Sabe>,Tg(Amh-cre/ERT)#Sabe/0	B6JJcl.Cg-Nrg1<tm1Sabe> Tg(Amh-cre/ERT)#Sabe	N	21715427
MGI:5292112	M	MP:0008280	abnormal male germ cell apoptosis	Nrg1<tm1Sabe>/Nrg1<tm1Sabe>,Tg(Amh-cre/ERT)#Sabe/0	B6JJcl.Cg-Nrg1<tm1Sabe> Tg(Amh-cre/ERT)#Sabe	N	21715427
MGI:5292112	M	MP:0002216	abnormal seminiferous tubule morphology	Nrg1<tm1Sabe>/Nrg1<tm1Sabe>,Tg(Amh-cre/ERT)#Sabe/0	B6JJcl.Cg-Nrg1<tm1Sabe> Tg(Amh-cre/ERT)#Sabe	N	21715427
MGI:5292347	M	MP:0001925	male infertility	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292347	F	MP:0013607	ovary fibrosis	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292347	M	MP:0001147	small testis	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292347	F	MP:0005168	abnormal female meiosis	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292347	F	MP:0004833	ovary atrophy	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292347	F	MP:0005431	decreased oocyte number	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292347	M	MP:0008261	arrest of male meiosis	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292347	F	MP:0002682	decreased mature ovarian follicle number	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292347	M	MP:0005159	azoospermia	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292347	M	MP:0001155	arrest of spermatogenesis	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292347	F	MP:0011122	absent primordial ovarian follicles	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292347	M	MP:0008280	abnormal male germ cell apoptosis	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292347	F	MP:0001923	reduced female fertility	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292347	M	MP:0005169	abnormal male meiosis	Rad21l<tm1Amp>/Rad21l<tm1Amp>	involves: 129S6/SvEvTac * C57BL/6NCr	N	21743440
MGI:5292357	M	MP:0002206	abnormal CNS synaptic transmission	Fmr1<tm1.2Cidz>/Y	involves: 129P2/OlaHsd * 129/Sv * C57BL/6 * FVB/N	N	19103683
MGI:5292357	M	MP:0009940	abnormal hippocampus pyramidal cell morphology	Fmr1<tm1.2Cidz>/Y	involves: 129P2/OlaHsd * 129/Sv * C57BL/6 * FVB/N	N	19103683
MGI:5292357	M	MP:0004753	abnormal miniature excitatory postsynaptic currents	Fmr1<tm1.2Cidz>/Y	involves: 129P2/OlaHsd * 129/Sv * C57BL/6 * FVB/N	N	19103683
MGI:5292357	M	MP:0003008	enhanced long-term potentiation	Fmr1<tm1.2Cidz>/Y	involves: 129P2/OlaHsd * 129/Sv * C57BL/6 * FVB/N	N	19103683
MGI:5292390	M	MP:0008261	arrest of male meiosis	Mybl1<repro9>/Mybl1<repro9>	involves: C3HeB/FeJ * C57BL/6J	N	21750041
MGI:5292390	M	MP:0005159	azoospermia	Mybl1<repro9>/Mybl1<repro9>	involves: C3HeB/FeJ * C57BL/6J	N	21750041
MGI:5292390	M	MP:0008280	abnormal male germ cell apoptosis	Mybl1<repro9>/Mybl1<repro9>	involves: C3HeB/FeJ * C57BL/6J	N	21750041
MGI:5292390	M	MP:0001147	small testis	Mybl1<repro9>/Mybl1<repro9>	involves: C3HeB/FeJ * C57BL/6J	N	21750041
MGI:5292390	F	MP:0005389	reproductive system phenotype	Mybl1<repro9>/Mybl1<repro9>	involves: C3HeB/FeJ * C57BL/6J	Y	21750041
MGI:5292390	M	MP:0001925	male infertility	Mybl1<repro9>/Mybl1<repro9>	involves: C3HeB/FeJ * C57BL/6J	N	21750041
MGI:5292391	M	MP:0008261	arrest of male meiosis	Mybl1<repro9>/Mybl1<tm1Epr>	involves: C3HeB/FeJ * C57BL/6J	N	21750041
MGI:5292391	M	MP:0001146	abnormal testis morphology	Mybl1<repro9>/Mybl1<tm1Epr>	involves: C3HeB/FeJ * C57BL/6J	N	21750041
MGI:5292391	M	MP:0005159	azoospermia	Mybl1<repro9>/Mybl1<tm1Epr>	involves: C3HeB/FeJ * C57BL/6J	N	21750041
MGI:5292391	M	MP:0001925	male infertility	Mybl1<repro9>/Mybl1<tm1Epr>	involves: C3HeB/FeJ * C57BL/6J	N	21750041
MGI:5292535	F	MP:0005458	increased percent body fat/body weight	Col2a1<M2J>/Col2a1<+>	B6;C3Fe-Col2a1<M2J>/GrsrJ	N	MGI:5436322
MGI:5292535	F	MP:0001260	increased body weight	Col2a1<M2J>/Col2a1<+>	B6;C3Fe-Col2a1<M2J>/GrsrJ	N	MGI:5436322
MGI:5292535	M	MP:0005459	decreased percent body fat/body weight	Col2a1<M2J>/Col2a1<+>	B6;C3Fe-Col2a1<M2J>/GrsrJ	N	MGI:5436322
MGI:5292677	M	MP:0004852	decreased testis weight	Nr5a1<tm1.1Hain>/Nr5a1<tm1.1Hain>	Not Specified	N	21820362
MGI:5292677	M	MP:0001154	seminiferous tubule degeneration	Nr5a1<tm1.1Hain>/Nr5a1<tm1.1Hain>	Not Specified	N	21820362
MGI:5292677	M	MP:0001146	abnormal testis morphology	Nr5a1<tm1.1Hain>/Nr5a1<tm1.1Hain>	Not Specified	N	21820362
MGI:5292677	M	MP:0002687	oligozoospermia	Nr5a1<tm1.1Hain>/Nr5a1<tm1.1Hain>	Not Specified	N	21820362
MGI:5292677	F	MP:0001926	female infertility	Nr5a1<tm1.1Hain>/Nr5a1<tm1.1Hain>	Not Specified	N	21820362
MGI:5292677	M	MP:0001925	male infertility	Nr5a1<tm1.1Hain>/Nr5a1<tm1.1Hain>	Not Specified	N	21820362
MGI:5292677	M	MP:0001152	increased Leydig cell number	Nr5a1<tm1.1Hain>/Nr5a1<tm1.1Hain>	Not Specified	N	21820362
MGI:5292677	M	MP:0003830	abnormal testis development	Nr5a1<tm1.1Hain>/Nr5a1<tm1.1Hain>	Not Specified	N	21820362
MGI:5293401	F	MP:0002816	colitis	Cyld<tm1.1Mpa>/Cyld<tm1.1Mpa>,Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Vil1-cre)997Gum/0	B6.Cg-Cyld<tm1.1Mpa> Ikbkg<tm1.1Mpa> Tg(Vil1-cre)997Gum	N	21804564
MGI:5293401	F	MP:0000491	crypts of Lieberkuhn abscesses	Cyld<tm1.1Mpa>/Cyld<tm1.1Mpa>,Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Vil1-cre)997Gum/0	B6.Cg-Cyld<tm1.1Mpa> Ikbkg<tm1.1Mpa> Tg(Vil1-cre)997Gum	N	21804564
MGI:5293402	M	MP:0002816	colitis	Cyld<tm1.1Mpa>/Cyld<tm1.1Mpa>,Ikbkg<tm1.1Mpa>/Y,Tg(Vil1-cre)997Gum/0	B6.Cg-Cyld<tm1.1Mpa> Ikbkg<tm1.1Mpa> Tg(Vil1-cre)997Gum	N	21804564
MGI:5293402	M	MP:0000491	crypts of Lieberkuhn abscesses	Cyld<tm1.1Mpa>/Cyld<tm1.1Mpa>,Ikbkg<tm1.1Mpa>/Y,Tg(Vil1-cre)997Gum/0	B6.Cg-Cyld<tm1.1Mpa> Ikbkg<tm1.1Mpa> Tg(Vil1-cre)997Gum	N	21804564
MGI:5293403	F	MP:0002816	colitis	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Vil1-cre)997Gum/0	B6.Cg-Ikbkg<tm1.1Mpa> Tg(Vil1-cre)997Gum	N	21804564
MGI:5293403	F	MP:0000491	crypts of Lieberkuhn abscesses	Ikbkg<tm1.1Mpa>/Ikbkg<tm1.1Mpa>,Tg(Vil1-cre)997Gum/0	B6.Cg-Ikbkg<tm1.1Mpa> Tg(Vil1-cre)997Gum	N	21804564
MGI:5293406	M	MP:0002816	colitis	Ikbkg<tm1.1Mpa>/Y,Tg(Vil1-cre)997Gum/0	B6.Cg-Ikbkg<tm1.1Mpa> Tg(Vil1-cre)997Gum	N	21804564
MGI:5293406	M	MP:0000491	crypts of Lieberkuhn abscesses	Ikbkg<tm1.1Mpa>/Y,Tg(Vil1-cre)997Gum/0	B6.Cg-Ikbkg<tm1.1Mpa> Tg(Vil1-cre)997Gum	N	21804564
MGI:5293439	F	MP:0001382	abnormal nursing	Mapk1<tm1.2Kuta>/Mapk1<tm1.2Kuta>,Tg(Nes-cre)1Kag/0	involves: 129P2/OlaHsd * C57BL/6J	N	21849556
MGI:5293439	F	MP:0001386	abnormal maternal nurturing	Mapk1<tm1.2Kuta>/Mapk1<tm1.2Kuta>,Tg(Nes-cre)1Kag/0	involves: 129P2/OlaHsd * C57BL/6J	N	21849556
MGI:5293642	F	MP:0012431	increased lymphoma incidence	Tmprss11d<tm1Bug>/Tmprss11d<tm1Bug>	involves: 129S1/Sv * 129X1/SvJ * NIH Black Swiss	N	21853097
MGI:5293643	M	MP:0000659	prostate gland hyperplasia	Tmprss11a<tm1Dgen>/Tmprss11a<tm1Dgen>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21853097
MGI:5293826	M	MP:0001147	small testis	Tsx<tm1.2Jtl>/Y	B6.129S(FVB)-Tsx<tm1.2Jtl>	N	21912526
MGI:5293826	M	MP:0001940	testis hypoplasia	Tsx<tm1.2Jtl>/Y	B6.129S(FVB)-Tsx<tm1.2Jtl>	N	21912526
MGI:5293826	M	MP:0009453	enhanced contextual conditioning behavior	Tsx<tm1.2Jtl>/Y	B6.129S(FVB)-Tsx<tm1.2Jtl>	N	21912526
MGI:5293827	F	MP:0001935	decreased litter size	Tsx<tm1.2Jtl>/Tsx<tm1.2Jtl>	B6.129S(FVB)-Tsx<tm1.2Jtl>	N	21912526
MGI:5293827	F	MP:0001923	reduced female fertility	Tsx<tm1.2Jtl>/Tsx<tm1.2Jtl>	B6.129S(FVB)-Tsx<tm1.2Jtl>	N	21912526
MGI:5293831	F	MP:0031213	increased eye anterior chamber depth	Fgf9<Aca12>/Fgf9<+>	involves: C57BL/6J	N	21858205
MGI:5294565	F	MP:0001923	reduced female fertility	Alpl<tm1(cre)Nagy>/Alpl<+>,Tet3<tm1.1Gxu>/Tet3<tm1.2Gxu>	involves: 129 * C57BL/6J * SJL	N	21892189
MGI:5294785	M	MP:0004851	increased testis weight	Gstk1<tm1Pgb>/Gstk1<tm1Pgb>	BALB/c-Gstk1<tm1Pgb>	N	21826057
MGI:5295221	M	MP:0005404	abnormal axon morphology	L1cam<tm1.1Pfm>/L1cam<tm1.1Pfm>	Not Specified	N	18171935
MGI:5295221	F	MP:0002961	abnormal axon guidance	L1cam<tm1.1Pfm>/L1cam<tm1.1Pfm>	Not Specified	N	18171935
MGI:5295221	F	MP:0008056	abnormal retina ganglion cell morphology	L1cam<tm1.1Pfm>/L1cam<tm1.1Pfm>	Not Specified	N	18171935
MGI:5295221	F	MP:0003631	nervous system phenotype	L1cam<tm1.1Pfm>/L1cam<tm1.1Pfm>	Not Specified	Y	18171935
MGI:5295222	M	MP:0002961	abnormal axon guidance	L1cam<tm1.1Pfm>/Y	Not Specified	N	18171935
MGI:5295222	M	MP:0008056	abnormal retina ganglion cell morphology	L1cam<tm1.1Pfm>/Y	Not Specified	N	18171935
MGI:5295222	M	MP:0003631	nervous system phenotype	L1cam<tm1.1Pfm>/Y	Not Specified	Y	18171935
MGI:5295264	M	MP:0002216	abnormal seminiferous tubule morphology	Usp2<tm1.1Ssw>/Usp2<tm1.1Ssw>	involves: C57BL/6	N	21543767
MGI:5295264	M	MP:0002674	abnormal sperm motility	Usp2<tm1.1Ssw>/Usp2<tm1.1Ssw>	involves: C57BL/6	N	21543767
MGI:5295264	M	MP:0006362	abnormal male germ cell morphology	Usp2<tm1.1Ssw>/Usp2<tm1.1Ssw>	involves: C57BL/6	N	21543767
MGI:5295264	M	MP:0001922	reduced male fertility	Usp2<tm1.1Ssw>/Usp2<tm1.1Ssw>	involves: C57BL/6	N	21543767
MGI:5295269	M	MP:0001925	male infertility	Spef2<bgh>/Spef2<bgh>	involves: C57BL/6J * C57BL/10J	N	21715716
MGI:5295270	M	MP:0014465	abnormal sperm mitochondrial morphology	Spef2<bgh>/Spef2<bgh>	involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J	N	21715716
MGI:5295270	M	MP:0001925	male infertility	Spef2<bgh>/Spef2<bgh>	involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J	N	21715716
MGI:5295270	M	MP:0001156	abnormal spermatogenesis	Spef2<bgh>/Spef2<bgh>	involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J	N	21715716
MGI:5295270	M	MP:0008892	abnormal sperm flagellum morphology	Spef2<bgh>/Spef2<bgh>	involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J	N	21715716
MGI:5295270	M	MP:0009838	abnormal sperm axoneme morphology	Spef2<bgh>/Spef2<bgh>	involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J	N	21715716
MGI:5295270	M	MP:0030590	abnormal sperm fibrous sheath morphology	Spef2<bgh>/Spef2<bgh>	involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J	N	21715716
MGI:5295270	M	MP:0009239	short sperm flagellum	Spef2<bgh>/Spef2<bgh>	involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J	N	21715716
MGI:5295270	F	MP:0005389	reproductive system phenotype	Spef2<bgh>/Spef2<bgh>	involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J	Y	21715716
MGI:5295270	M	MP:0002687	oligozoospermia	Spef2<bgh>/Spef2<bgh>	involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J	N	21715716
MGI:5295295	M	MP:0005169	abnormal male meiosis	Spo11<tm1Nki>/Spo11<tm1Nki>	involves: 129P2/OlaHsd	N	21807948
MGI:5295295	F	MP:0001926	female infertility	Spo11<tm1Nki>/Spo11<tm1Nki>	involves: 129P2/OlaHsd	N	21807948
MGI:5295295	M	MP:0001925	male infertility	Spo11<tm1Nki>/Spo11<tm1Nki>	involves: 129P2/OlaHsd	N	21807948
MGI:5295295	F	MP:0005168	abnormal female meiosis	Spo11<tm1Nki>/Spo11<tm1Nki>	involves: 129P2/OlaHsd	N	21807948
MGI:5295411	F	MP:0012411	increased granulosa cell tumor incidence	Atad5<Gt(RRF055)Byg>/Atad5<+>	involves: 129P2/OlaHsd	N	21901109
MGI:5295417	M	MP:0006378	abnormal spermatogonia morphology	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(AW0655)Wtsi>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295417	F	MP:0008000	increased ovary tumor incidence	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(AW0655)Wtsi>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295417	M	MP:0004901	decreased male germ cell number	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(AW0655)Wtsi>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295417	F	MP:0001128	ovary hyperplasia	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(AW0655)Wtsi>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295417	M	MP:0002216	abnormal seminiferous tubule morphology	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(AW0655)Wtsi>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295417	F	MP:0001926	female infertility	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(AW0655)Wtsi>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295417	F	MP:0031020	premature ovarian failure	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(AW0655)Wtsi>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295417	M	MP:0001147	small testis	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(AW0655)Wtsi>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295417	M	MP:0002687	oligozoospermia	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(AW0655)Wtsi>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295417	M	MP:0008261	arrest of male meiosis	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(AW0655)Wtsi>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295418	M	MP:0002216	abnormal seminiferous tubule morphology	Mcm9<Gt(XG743)Byg>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295418	F	MP:0005431	decreased oocyte number	Mcm9<Gt(XG743)Byg>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295418	M	MP:0008261	arrest of male meiosis	Mcm9<Gt(XG743)Byg>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295418	M	MP:0004901	decreased male germ cell number	Mcm9<Gt(XG743)Byg>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295418	F	MP:0008000	increased ovary tumor incidence	Mcm9<Gt(XG743)Byg>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295418	F	MP:0008871	abnormal ovarian follicle number	Mcm9<Gt(XG743)Byg>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295418	F	MP:0006361	abnormal female germ cell morphology	Mcm9<Gt(XG743)Byg>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295418	F	MP:0011121	decreased primordial ovarian follicle number	Mcm9<Gt(XG743)Byg>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295418	M	MP:0001147	small testis	Mcm9<Gt(XG743)Byg>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295418	M	MP:0002687	oligozoospermia	Mcm9<Gt(XG743)Byg>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295418	M	MP:0006378	abnormal spermatogonia morphology	Mcm9<Gt(XG743)Byg>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295419	M	MP:0002216	abnormal seminiferous tubule morphology	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295419	M	MP:0001147	small testis	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295419	M	MP:0004901	decreased male germ cell number	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295419	F	MP:0008000	increased ovary tumor incidence	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295419	M	MP:0008261	arrest of male meiosis	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295419	M	MP:0002687	oligozoospermia	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295419	M	MP:0006378	abnormal spermatogonia morphology	Mcm9<Gt(AW0655)Wtsi>/Mcm9<Gt(XG743)Byg>	involves: 129P2/OlaHsd * C3HeB/FeJ	N	21987787
MGI:5295464	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Hprt1<tm1(CAG-cre)Mnn>/Hprt1<+>,Ptpn11<tm1Ckq>/Ptpn11<+>	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6J	N	21930766
MGI:5295464	F	MP:0000270	abnormal heart tube morphology	Hprt1<tm1(CAG-cre)Mnn>/Hprt1<+>,Ptpn11<tm1Ckq>/Ptpn11<+>	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6J	N	21930766
MGI:5295464	F	MP:0003984	embryonic growth retardation	Hprt1<tm1(CAG-cre)Mnn>/Hprt1<+>,Ptpn11<tm1Ckq>/Ptpn11<+>	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6J	N	21930766
MGI:5295464	F	MP:0003935	abnormal craniofacial development	Hprt1<tm1(CAG-cre)Mnn>/Hprt1<+>,Ptpn11<tm1Ckq>/Ptpn11<+>	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6J	N	21930766
MGI:5295642	M	MP:0003179	thrombocytopenia	Gata1<tm1Mym>/Y,Tg(Gata1*V205G)1Mym/0	involves: C57BL/6 * DBA/2	N	14656885
MGI:5295642	M	MP:0008254	increased megakaryocyte cell number	Gata1<tm1Mym>/Y,Tg(Gata1*V205G)1Mym/0	involves: C57BL/6 * DBA/2	N	14656885
MGI:5295642	M	MP:0002447	abnormal erythrocyte morphology	Gata1<tm1Mym>/Y,Tg(Gata1*V205G)1Mym/0	involves: C57BL/6 * DBA/2	N	14656885
MGI:5295642	M	MP:0004200	decreased fetal size	Gata1<tm1Mym>/Y,Tg(Gata1*V205G)1Mym/0	involves: C57BL/6 * DBA/2	N	14656885
MGI:5295642	M	MP:0000229	abnormal megakaryocyte differentiation	Gata1<tm1Mym>/Y,Tg(Gata1*V205G)1Mym/0	involves: C57BL/6 * DBA/2	N	14656885
MGI:5295642	M	MP:0000228	abnormal thrombopoiesis	Gata1<tm1Mym>/Y,Tg(Gata1*V205G)1Mym/0	involves: C57BL/6 * DBA/2	N	14656885
MGI:5295642	M	MP:0002398	abnormal bone marrow cell morphology/development	Gata1<tm1Mym>/Y,Tg(Gata1*V205G)1Mym/0	involves: C57BL/6 * DBA/2	N	14656885
MGI:5295642	M	MP:0031276	abnormal stress erythropoiesis	Gata1<tm1Mym>/Y,Tg(Gata1*V205G)1Mym/0	involves: C57BL/6 * DBA/2	N	14656885
MGI:5295642	M	MP:0002642	anisocytosis	Gata1<tm1Mym>/Y,Tg(Gata1*V205G)1Mym/0	involves: C57BL/6 * DBA/2	N	14656885
MGI:5295642	M	MP:0002417	abnormal megakaryocyte morphology	Gata1<tm1Mym>/Y,Tg(Gata1*V205G)1Mym/0	involves: C57BL/6 * DBA/2	N	14656885
MGI:5295642	M	MP:0003717	pallor	Gata1<tm1Mym>/Y,Tg(Gata1*V205G)1Mym/0	involves: C57BL/6 * DBA/2	N	14656885
MGI:5295642	M	MP:0004720	abnormal platelet morphology	Gata1<tm1Mym>/Y,Tg(Gata1*V205G)1Mym/0	involves: C57BL/6 * DBA/2	N	14656885
MGI:5295642	M	MP:0008247	abnormal mononuclear cell morphology	Gata1<tm1Mym>/Y,Tg(Gata1*V205G)1Mym/0	involves: C57BL/6 * DBA/2	N	14656885
MGI:5295749	M	MP:0010522	calcified aorta	Lmna<tm1.1Otin>/Lmna<tm1.1Otin>	involves: 129P2/OlaHsd * C57BL/6	N	23690466
MGI:5295853	M	MP:0004929	decreased epididymis weight	Gt(ROSA)26Sor<tm1(RNU6-RNAi:Rad18)Wbaa>/Gt(ROSA)26Sor<+>	involves: 129S6/SvEvTac * C57BL/6	N	21807948
MGI:5295853	M	MP:0006380	abnormal spermatid morphology	Gt(ROSA)26Sor<tm1(RNU6-RNAi:Rad18)Wbaa>/Gt(ROSA)26Sor<+>	involves: 129S6/SvEvTac * C57BL/6	N	21807948
MGI:5295853	M	MP:0002687	oligozoospermia	Gt(ROSA)26Sor<tm1(RNU6-RNAi:Rad18)Wbaa>/Gt(ROSA)26Sor<+>	involves: 129S6/SvEvTac * C57BL/6	N	21807948
MGI:5295853	M	MP:0004852	decreased testis weight	Gt(ROSA)26Sor<tm1(RNU6-RNAi:Rad18)Wbaa>/Gt(ROSA)26Sor<+>	involves: 129S6/SvEvTac * C57BL/6	N	21807948
MGI:5295945	M	MP:0003557	absent vas deferens	Pax2<tm1Mbu>/Pax2<+>,Pax8<tm1(cre)Mbu>/Pax8<tm1(cre)Mbu>	involves: 129P2/OlaHsd * C3H/He * C57BL/6	N	12435636
MGI:5295977	F	MP:0001926	female infertility	Cep290<tm1.1Jgg>/Cep290<tm1.1Jgg>	B6.129-Cep290<tm1.1Jgg>	N	MGI:3606206
MGI:5295977	M	MP:0001925	male infertility	Cep290<tm1.1Jgg>/Cep290<tm1.1Jgg>	B6.129-Cep290<tm1.1Jgg>	N	MGI:3606206
MGI:5296000	M	MP:0001922	reduced male fertility	Kcnn2<fri>/Kcnn2<fri>	129S2.C3Pas-Kcnn2<fri>	N	18604572
MGI:5296673	M	MP:0001147	small testis	Plk4<Gt(XK603)Byg>/Plk4<+>	involves: 129P2/OlaHsd	N	21791561
MGI:5296676	M	MP:0004852	decreased testis weight	Plk4<m1Lja>/Plk4<+>	C57BL/6J-Plk4<m1Lja>	N	21791561
MGI:5296676	M	MP:0004901	decreased male germ cell number	Plk4<m1Lja>/Plk4<+>	C57BL/6J-Plk4<m1Lja>	N	21791561
MGI:5296676	M	MP:0001147	small testis	Plk4<m1Lja>/Plk4<+>	C57BL/6J-Plk4<m1Lja>	N	21791561
MGI:5296680	F	MP:0005397	hematopoietic system phenotype	Csf1<tm1.1(CSF1)Flv>/Csf1<tm1.1(CSF1)Flv>,Il2rg<tm1.1Flv>/Il2rg<tm1.1Flv>,Rag2<tm1.1Flv>/Rag2<tm1.1Flv>	involves: 129P2/OlaHsd * 129S/SvEv * 129S4/SvJae * BALB/cAnNTac	Y	21791433
MGI:5296680	F	MP:0005390	skeleton phenotype	Csf1<tm1.1(CSF1)Flv>/Csf1<tm1.1(CSF1)Flv>,Il2rg<tm1.1Flv>/Il2rg<tm1.1Flv>,Rag2<tm1.1Flv>/Rag2<tm1.1Flv>	involves: 129P2/OlaHsd * 129S/SvEv * 129S4/SvJae * BALB/cAnNTac	Y	21791433
MGI:5296680	F	MP:0005387	immune system phenotype	Csf1<tm1.1(CSF1)Flv>/Csf1<tm1.1(CSF1)Flv>,Il2rg<tm1.1Flv>/Il2rg<tm1.1Flv>,Rag2<tm1.1Flv>/Rag2<tm1.1Flv>	involves: 129P2/OlaHsd * 129S/SvEv * 129S4/SvJae * BALB/cAnNTac	Y	21791433
MGI:5296680	F	MP:0001790	abnormal immune system physiology	Csf1<tm1.1(CSF1)Flv>/Csf1<tm1.1(CSF1)Flv>,Il2rg<tm1.1Flv>/Il2rg<tm1.1Flv>,Rag2<tm1.1Flv>/Rag2<tm1.1Flv>	involves: 129P2/OlaHsd * 129S/SvEv * 129S4/SvJae * BALB/cAnNTac	N	21791433
MGI:5296680	F	MP:0005382	craniofacial phenotype	Csf1<tm1.1(CSF1)Flv>/Csf1<tm1.1(CSF1)Flv>,Il2rg<tm1.1Flv>/Il2rg<tm1.1Flv>,Rag2<tm1.1Flv>/Rag2<tm1.1Flv>	involves: 129P2/OlaHsd * 129S/SvEv * 129S4/SvJae * BALB/cAnNTac	Y	21791433
MGI:5296757	M	MP:0002769	abnormal vas deferens morphology	Tg(MMTVtTA)1Mam/0,Tg(tetO-Esr1)#Paf/0	involves: C57BL/6 * FVB/N * SJL	N	12212839
MGI:5296757	M	MP:0004929	decreased epididymis weight	Tg(MMTVtTA)1Mam/0,Tg(tetO-Esr1)#Paf/0	involves: C57BL/6 * FVB/N * SJL	N	12212839
MGI:5296757	F	MP:0009018	short estrus	Tg(MMTVtTA)1Mam/0,Tg(tetO-Esr1)#Paf/0	involves: C57BL/6 * FVB/N * SJL	N	12212839
MGI:5296757	M	MP:0002059	abnormal seminal vesicle morphology	Tg(MMTVtTA)1Mam/0,Tg(tetO-Esr1)#Paf/0	involves: C57BL/6 * FVB/N * SJL	N	12212839
MGI:5296787	F	MP:0001800	abnormal humoral immune response	Sh3kbp1<tm1Kuro>/Sh3kbp1<tm1Kuro>,Cd79a<tm1(cre)Reth>/Cd79a<+>	involves: BALB/c * C57BL/6 * NZB	N	21708930
MGI:5296787	F	MP:0010228	decreased transitional stage T3 B cell number	Sh3kbp1<tm1Kuro>/Sh3kbp1<tm1Kuro>,Cd79a<tm1(cre)Reth>/Cd79a<+>	involves: BALB/c * C57BL/6 * NZB	N	21708930
MGI:5296787	F	MP:0008174	decreased follicular B cell number	Sh3kbp1<tm1Kuro>/Sh3kbp1<tm1Kuro>,Cd79a<tm1(cre)Reth>/Cd79a<+>	involves: BALB/c * C57BL/6 * NZB	N	21708930
MGI:5296787	F	MP:0005017	decreased B cell number	Sh3kbp1<tm1Kuro>/Sh3kbp1<tm1Kuro>,Cd79a<tm1(cre)Reth>/Cd79a<+>	involves: BALB/c * C57BL/6 * NZB	N	21708930
MGI:5296787	F	MP:0008215	decreased immature B cell number	Sh3kbp1<tm1Kuro>/Sh3kbp1<tm1Kuro>,Cd79a<tm1(cre)Reth>/Cd79a<+>	involves: BALB/c * C57BL/6 * NZB	N	21708930
MGI:5296787	F	MP:0008168	decreased B-1a cell number	Sh3kbp1<tm1Kuro>/Sh3kbp1<tm1Kuro>,Cd79a<tm1(cre)Reth>/Cd79a<+>	involves: BALB/c * C57BL/6 * NZB	N	21708930
MGI:5296787	F	MP:0000717	abnormal lymphocyte cell number	Sh3kbp1<tm1Kuro>/Sh3kbp1<tm1Kuro>,Cd79a<tm1(cre)Reth>/Cd79a<+>	involves: BALB/c * C57BL/6 * NZB	N	21708930
MGI:5296787	F	MP:0002459	abnormal B cell physiology	Sh3kbp1<tm1Kuro>/Sh3kbp1<tm1Kuro>,Cd79a<tm1(cre)Reth>/Cd79a<+>	involves: BALB/c * C57BL/6 * NZB	N	21708930
MGI:5296787	F	MP:0009926	decreased transitional stage T2 B cell number	Sh3kbp1<tm1Kuro>/Sh3kbp1<tm1Kuro>,Cd79a<tm1(cre)Reth>/Cd79a<+>	involves: BALB/c * C57BL/6 * NZB	N	21708930
MGI:5296787	F	MP:0005387	immune system phenotype	Sh3kbp1<tm1Kuro>/Sh3kbp1<tm1Kuro>,Cd79a<tm1(cre)Reth>/Cd79a<+>	involves: BALB/c * C57BL/6 * NZB	Y	21708930
MGI:5296788	F	MP:0008168	decreased B-1a cell number	Sh3kbp1<tm1Kuro>/Sh3kbp1<tm1Kuro>,Cd79a<tm1(cre)Reth>/Cd79a<+>,Gt(ROSA)26Sor<tm4(Ikbkb)Rsky>/?	involves: BALB/c * C57BL/6 * NZB	N	21708930
MGI:5296788	F	MP:0005387	immune system phenotype	Sh3kbp1<tm1Kuro>/Sh3kbp1<tm1Kuro>,Cd79a<tm1(cre)Reth>/Cd79a<+>,Gt(ROSA)26Sor<tm4(Ikbkb)Rsky>/?	involves: BALB/c * C57BL/6 * NZB	Y	21708930
MGI:5296806	F	MP:0009505	abnormal mammary gland lobule morphology	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-Esr1)#Paf/0	involves: FVB/N	N	15705859
MGI:5296806	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-Esr1)#Paf/0	involves: FVB/N	N	15705859
MGI:5296806	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-Esr1)#Paf/0	involves: FVB/N	N	15705859
MGI:5296806	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-Esr1)#Paf/0	involves: FVB/N	N	15705859
MGI:5296806	F	MP:0009504	abnormal mammary gland epithelium morphology	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-Esr1)#Paf/0	involves: FVB/N	N	15705859
MGI:5296806	F	MP:0001885	mammary gland duct hyperplasia	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-Esr1)#Paf/0	involves: FVB/N	N	15705859
MGI:5296806	F	MP:0009503	abnormal mammary gland duct morphology	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-Esr1)#Paf/0	involves: FVB/N	N	15705859
MGI:5296941	M	MP:0001147	small testis	Sox2<tm3(TK)Hoch>/Sox2<+>	involves: 129S4/SvJae * C57BL/6	N	21982232
MGI:5296941	M	MP:0004901	decreased male germ cell number	Sox2<tm3(TK)Hoch>/Sox2<+>	involves: 129S4/SvJae * C57BL/6	N	21982232
MGI:5296964	F	MP:0010698	abnormal impulsive behavior control	Disc1<tm1Kozo>/Disc1<tm1Kozo>	B6JJmsSlc.Cg-Disc1<tm1Kozo>	N	21903668
MGI:5296964	F	MP:0009142	decreased prepulse inhibition	Disc1<tm1Kozo>/Disc1<tm1Kozo>	B6JJmsSlc.Cg-Disc1<tm1Kozo>	N	21903668
MGI:5296964	M	MP:0003461	abnormal response to novel object	Disc1<tm1Kozo>/Disc1<tm1Kozo>	B6JJmsSlc.Cg-Disc1<tm1Kozo>	N	21903668
MGI:5297133	F	MP:0009503	abnormal mammary gland duct morphology	Brca1<tm2Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0	involves: 129S6/SvEvTac * C57BL/6 * FVB	N	17653086
MGI:5297133	F	MP:0010173	increased mammary gland epithelial cell proliferation	Brca1<tm2Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0	involves: 129S6/SvEvTac * C57BL/6 * FVB	N	17653086
MGI:5297133	F	MP:0001884	mammary gland alveolar hyperplasia	Brca1<tm2Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0	involves: 129S6/SvEvTac * C57BL/6 * FVB	N	17653086
MGI:5297134	F	MP:0010173	increased mammary gland epithelial cell proliferation	Brca1<tm2Cxd>/Brca1<tm2Cxd>,Trp53<tm1Brd>/Trp53<+>,Tg(MMTV-cre)4Mam/0	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB	N	17653086
MGI:5297134	F	MP:0001884	mammary gland alveolar hyperplasia	Brca1<tm2Cxd>/Brca1<tm2Cxd>,Trp53<tm1Brd>/Trp53<+>,Tg(MMTV-cre)4Mam/0	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB	N	17653086
MGI:5297135	F	MP:0001884	mammary gland alveolar hyperplasia	Brca1<tm2Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0,Tg(MMTV-rtTA)1Lach/0,Tg(tetO-Esr1)#Paf/0,Trp53<tm1Brd>/Trp53<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB	N	17653086
MGI:5297558	F	MP:0020010	decreased bone mineral density of femur	Pth1r<tm2Hmk>/Pth1r<tm2Hmk>,Tg(Dmp1-cre/ERT2)0022Pdp/0	involves: 129S4/SvJae * C3H * C57BL/6	N	21220409
MGI:5297558	F	MP:0021186	decreased bone mineral density of vertebrae	Pth1r<tm2Hmk>/Pth1r<tm2Hmk>,Tg(Dmp1-cre/ERT2)0022Pdp/0	involves: 129S4/SvJae * C3H * C57BL/6	N	21220409
MGI:5297583	F	MP:0005431	decreased oocyte number	Nbn<tm1Nus>/Nbn<tm2Nus>,Tg(Spo11-cre)D5Mpel/0	involves: BALB/c * C57BL/6	N	21147852
MGI:5297583	F	MP:0001127	small ovary	Nbn<tm1Nus>/Nbn<tm2Nus>,Tg(Spo11-cre)D5Mpel/0	involves: BALB/c * C57BL/6	N	21147852
MGI:5297584	M	MP:0014052	increased male germ cell apoptosis	Jam3<tm1Rha>/Jam3<tm1.1Chav>,Tg(Spo11-cre)D5Mpel/0	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	21147852
MGI:5297584	M	MP:0001155	arrest of spermatogenesis	Jam3<tm1Rha>/Jam3<tm1.1Chav>,Tg(Spo11-cre)D5Mpel/0	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	21147852
MGI:5297584	M	MP:0004901	decreased male germ cell number	Jam3<tm1Rha>/Jam3<tm1.1Chav>,Tg(Spo11-cre)D5Mpel/0	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	21147852
MGI:5297584	M	MP:0009376	abnormal manchette morphology	Jam3<tm1Rha>/Jam3<tm1.1Chav>,Tg(Spo11-cre)D5Mpel/0	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	21147852
MGI:5297584	M	MP:0006380	abnormal spermatid morphology	Jam3<tm1Rha>/Jam3<tm1.1Chav>,Tg(Spo11-cre)D5Mpel/0	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	21147852
MGI:5297584	M	MP:0001147	small testis	Jam3<tm1Rha>/Jam3<tm1.1Chav>,Tg(Spo11-cre)D5Mpel/0	involves: 129P2/OlaHsd * BALB/c * C57BL/6	N	21147852
MGI:5297585	M	MP:0010357	increased prostate gland tumor incidence	Sirt2<tm1.1Cxd>/Sirt2<tm1.1Cxd>	either: (involves: C57BL/6 * FVB/N) or (involves: FVB/N * NIH Black Swiss)	N	22014574
MGI:5297585	F	MP:0000630	mammary gland hyperplasia	Sirt2<tm1.1Cxd>/Sirt2<tm1.1Cxd>	either: (involves: C57BL/6 * FVB/N) or (involves: FVB/N * NIH Black Swiss)	N	22014574
MGI:5297727	M	MP:0000473	abnormal stomach glandular epithelium morphology	Vsig1<tm1Imad>/Y	chimera involves: 129S1/Sv * 129X1/Sv	N	21991385
MGI:5297818	F	MP:0001923	reduced female fertility	Nkx2-2<tm2.1Suss>/Nkx2-2<tm2.1Suss>	involves: 129S6/SvEvTac * Black Swiss * C57BL/6 * C57BL/6J * SJL	N	22056672
MGI:5297818	M	MP:0001922	reduced male fertility	Nkx2-2<tm2.1Suss>/Nkx2-2<tm2.1Suss>	involves: 129S6/SvEvTac * Black Swiss * C57BL/6 * C57BL/6J * SJL	N	22056672
MGI:5297819	F	MP:0005379	endocrine/exocrine gland phenotype	Arx<tm1Gldn>/Arx<tm1Gldn>,Nkx2-2<tm2.1Suss>/Nkx2-2<tm2.1Suss>,Tg(Ins2-cre)23Herr/0	involves: 129 * Black Swiss * C57BL/6 * CBA/J * SJL	Y	22056672
MGI:5297819	F	MP:0003339	decreased pancreatic beta cell number	Arx<tm1Gldn>/Arx<tm1Gldn>,Nkx2-2<tm2.1Suss>/Nkx2-2<tm2.1Suss>,Tg(Ins2-cre)23Herr/0	involves: 129 * Black Swiss * C57BL/6 * CBA/J * SJL	N	22056672
MGI:5297819	F	MP:0001559	hyperglycemia	Arx<tm1Gldn>/Arx<tm1Gldn>,Nkx2-2<tm2.1Suss>/Nkx2-2<tm2.1Suss>,Tg(Ins2-cre)23Herr/0	involves: 129 * Black Swiss * C57BL/6 * CBA/J * SJL	N	22056672
MGI:5297961	M	MP:0002551	abnormal blood coagulation	F8<tm2Kaz>/Y,Tg(Alb-F8)EBmre/0	involves: 129S4/SvJae * C57BL/6J	N	21705497
MGI:5297962	M	MP:0002551	abnormal blood coagulation	F8<tm2Kaz>/Y	involves: 129S4/SvJae	N	21705497
MGI:5298089	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm75(Ple143-lacZ)Ems>/Y	B6.Cg-Hprt1<tm75(Ple143-lacZ)Ems>/Mmjax	N	MGI:3835781
MGI:5298517	M	MP:0001925	male infertility	Fgfr3<m1J>/Fgfr3<m1J>	CByJ.Cg-Fgfr3<m1J>/GrsrJ	N	MGI:5298490
MGI:5298845	M	MP:0006380	abnormal spermatid morphology	Htt<tm1Hay>/Htt<tm1Hay>,Tg(YAC72)2511Hay/0	involves: FVB/N	N	11133364
MGI:5298845	M	MP:0020550	multinucleated giant male germ cells	Htt<tm1Hay>/Htt<tm1Hay>,Tg(YAC72)2511Hay/0	involves: FVB/N	N	11133364
MGI:5298845	M	MP:0002687	oligozoospermia	Htt<tm1Hay>/Htt<tm1Hay>,Tg(YAC72)2511Hay/0	involves: FVB/N	N	11133364
MGI:5298845	M	MP:0008280	abnormal male germ cell apoptosis	Htt<tm1Hay>/Htt<tm1Hay>,Tg(YAC72)2511Hay/0	involves: FVB/N	N	11133364
MGI:5298845	F	MP:0005389	reproductive system phenotype	Htt<tm1Hay>/Htt<tm1Hay>,Tg(YAC72)2511Hay/0	involves: FVB/N	Y	11133364
MGI:5298845	M	MP:0003205	testicular atrophy	Htt<tm1Hay>/Htt<tm1Hay>,Tg(YAC72)2511Hay/0	involves: FVB/N	N	11133364
MGI:5298845	M	MP:0001925	male infertility	Htt<tm1Hay>/Htt<tm1Hay>,Tg(YAC72)2511Hay/0	involves: FVB/N	N	11133364
MGI:5298846	M	MP:0003205	testicular atrophy	Htt<tm1Hay>/Htt<+>,Tg(YAC72)2511Hay/0	involves: FVB/N	N	11133364
MGI:5298849	M	MP:0001925	male infertility	Htt<tm1Hay>/Htt<tm1Hay>,Tg(YAC46)668Hay/0	involves: FVB/N	N	11133364
MGI:5299159	M	MP:0002083	premature death	Mapt<tm1(Setdb1)Akba>/Mapt<+>,Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * FVB/N	N	20869373
MGI:5299159	M	MP:0001405	impaired coordination	Mapt<tm1(Setdb1)Akba>/Mapt<+>,Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * FVB/N	N	20869373
MGI:5299160	M	MP:0002083	premature death	Mapt<tm1(Setdb1)Akba>/Mapt<tm1(Setdb1)Akba>,Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * FVB/N	N	20869373
MGI:5299160	M	MP:0001405	impaired coordination	Mapt<tm1(Setdb1)Akba>/Mapt<tm1(Setdb1)Akba>,Mecp2<tm1Jae>/Y,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * FVB/N	N	20869373
MGI:5299161	M	MP:0002083	premature death	Mecp2<tm1Jae>/Y,Tg(Camk2a-Setdb1)1Akba/0,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL	N	20869373
MGI:5299161	M	MP:0001262	decreased body weight	Mecp2<tm1Jae>/Y,Tg(Camk2a-Setdb1)1Akba/0,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL	N	20869373
MGI:5299161	M	MP:0001402	decreased locomotor activity	Mecp2<tm1Jae>/Y,Tg(Camk2a-Setdb1)1Akba/0,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL	N	20869373
MGI:5299161	M	MP:0001405	impaired coordination	Mecp2<tm1Jae>/Y,Tg(Camk2a-Setdb1)1Akba/0,Tg(Nes-cre)1Atp/0	involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL	N	20869373
MGI:5299162	M	MP:0001262	decreased body weight	Mecp2<tm1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	20869373
MGI:5299162	M	MP:0001402	decreased locomotor activity	Mecp2<tm1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	20869373
MGI:5299162	M	MP:0002083	premature death	Mecp2<tm1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	20869373
MGI:5299162	M	MP:0001405	impaired coordination	Mecp2<tm1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	20869373
MGI:5299191	F	MP:0009503	abnormal mammary gland duct morphology	Phb2<tm2.1Katz>/Phb2<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	21862609
MGI:5299192	F	MP:0004047	abnormal milk composition	Phb2<tm2.1Katz>/Phb2<+>,Tg(Wap-cre)11738Mam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	21862609
MGI:5299192	F	MP:0001382	abnormal nursing	Phb2<tm2.1Katz>/Phb2<+>,Tg(Wap-cre)11738Mam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	21862609
MGI:5299193	F	MP:0000627	abnormal mammary gland morphology	Phb2<tm2.1Katz>/Phb2<tm2.1Katz>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	21862609
MGI:5299193	F	MP:0009503	abnormal mammary gland duct morphology	Phb2<tm2.1Katz>/Phb2<tm2.1Katz>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	21862609
MGI:5299194	F	MP:0006270	abnormal mammary gland growth during lactation	Phb2<tm2.1Katz>/Phb2<tm2.1Katz>,Tg(Wap-cre)11738Mam/0	involves: C57BL/6 * SJL	N	21862609
MGI:5299194	F	MP:0009506	abnormal mammary gland alveolus morphology	Phb2<tm2.1Katz>/Phb2<tm2.1Katz>,Tg(Wap-cre)11738Mam/0	involves: C57BL/6 * SJL	N	21862609
MGI:5299194	F	MP:0014126	increased mammary gland apoptosis	Phb2<tm2.1Katz>/Phb2<tm2.1Katz>,Tg(Wap-cre)11738Mam/0	involves: C57BL/6 * SJL	N	21862609
MGI:5299194	F	MP:0006271	abnormal involution of the mammary gland	Phb2<tm2.1Katz>/Phb2<tm2.1Katz>,Tg(Wap-cre)11738Mam/0	involves: C57BL/6 * SJL	N	21862609
MGI:5299194	F	MP:0001382	abnormal nursing	Phb2<tm2.1Katz>/Phb2<tm2.1Katz>,Tg(Wap-cre)11738Mam/0	involves: C57BL/6 * SJL	N	21862609
MGI:5299194	F	MP:0004047	abnormal milk composition	Phb2<tm2.1Katz>/Phb2<tm2.1Katz>,Tg(Wap-cre)11738Mam/0	involves: C57BL/6 * SJL	N	21862609
MGI:5299346	M	MP:0009415	skeletal muscle degeneration	Creb1<tm1.1Berd>/Creb1<tm1.1Berd>,Dmd<mdx>/Y	B.Cg-Creb1<tm1.1Berd> Dmd<mdx>	N	21931825
MGI:5299346	M	MP:0031318	enhanced skeletal muscle regeneration	Creb1<tm1.1Berd>/Creb1<tm1.1Berd>,Dmd<mdx>/Y	B.Cg-Creb1<tm1.1Berd> Dmd<mdx>	N	21931825
MGI:5300202	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Scrib<tm1.1Phum>/Scrib<tm1.1Phum>,Tg(Pbsn-cre)20Fwan/0	involves: FVB/NCrl	N	21965329
MGI:5300202	M	MP:0000659	prostate gland hyperplasia	Scrib<tm1.1Phum>/Scrib<tm1.1Phum>,Tg(Pbsn-cre)20Fwan/0	involves: FVB/NCrl	N	21965329
MGI:5300202	M	MP:0003607	abnormal prostate gland physiology	Scrib<tm1.1Phum>/Scrib<tm1.1Phum>,Tg(Pbsn-cre)20Fwan/0	involves: FVB/NCrl	N	21965329
MGI:5300203	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Kras<tm4Tyj>/Kras<+>,Tg(Pbsn-cre)20Fwan/0	involves: 129S4/SvJae * FVB/NCrl	N	21965329
MGI:5300203	M	MP:0003607	abnormal prostate gland physiology	Kras<tm4Tyj>/Kras<+>,Tg(Pbsn-cre)20Fwan/0	involves: 129S4/SvJae * FVB/NCrl	N	21965329
MGI:5300203	M	MP:0000659	prostate gland hyperplasia	Kras<tm4Tyj>/Kras<+>,Tg(Pbsn-cre)20Fwan/0	involves: 129S4/SvJae * FVB/NCrl	N	21965329
MGI:5300204	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Kras<tm4Tyj>/Kras<+>,Scrib<tm1.1Phum>/Scrib<tm1.1Phum>,Tg(Pbsn-cre)20Fwan/0	involves: 129S4/SvJae * FVB/NCrl	N	21965329
MGI:5300204	M	MP:0000659	prostate gland hyperplasia	Kras<tm4Tyj>/Kras<+>,Scrib<tm1.1Phum>/Scrib<tm1.1Phum>,Tg(Pbsn-cre)20Fwan/0	involves: 129S4/SvJae * FVB/NCrl	N	21965329
MGI:5300204	M	MP:0003607	abnormal prostate gland physiology	Kras<tm4Tyj>/Kras<+>,Scrib<tm1.1Phum>/Scrib<tm1.1Phum>,Tg(Pbsn-cre)20Fwan/0	involves: 129S4/SvJae * FVB/NCrl	N	21965329
MGI:5300204	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Kras<tm4Tyj>/Kras<+>,Scrib<tm1.1Phum>/Scrib<tm1.1Phum>,Tg(Pbsn-cre)20Fwan/0	involves: 129S4/SvJae * FVB/NCrl	N	21965329
MGI:5300205	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Kras<tm4Tyj>/Kras<+>,Scrib<tm1.1Phum>/Scrib<+>,Tg(Pbsn-cre)20Fwan/0	involves: 129S4/SvJae * FVB/NCrl	N	21965329
MGI:5300205	M	MP:0003607	abnormal prostate gland physiology	Kras<tm4Tyj>/Kras<+>,Scrib<tm1.1Phum>/Scrib<+>,Tg(Pbsn-cre)20Fwan/0	involves: 129S4/SvJae * FVB/NCrl	N	21965329
MGI:5300205	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Kras<tm4Tyj>/Kras<+>,Scrib<tm1.1Phum>/Scrib<+>,Tg(Pbsn-cre)20Fwan/0	involves: 129S4/SvJae * FVB/NCrl	N	21965329
MGI:5300207	M	MP:0003607	abnormal prostate gland physiology	Scrib<tm1.2Phum>/Scrib<+>	involves: FVB/N	N	21965329
MGI:5300207	M	MP:0004961	increased prostate gland weight	Scrib<tm1.2Phum>/Scrib<+>	involves: FVB/N	N	21965329
MGI:5300207	M	MP:0000659	prostate gland hyperplasia	Scrib<tm1.2Phum>/Scrib<+>	involves: FVB/N	N	21965329
MGI:5300579	F	MP:0010249	lactation failure	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Tg(MMTV-tTA)25755Kuw/0,Tg(tetO-Ccnd1*T286A,-luc)10897Kuw/0	involves: 129S2/SvPas * FVB/N	N	22037875
MGI:5300584	F	MP:0010249	lactation failure	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Tg(MMTV-tTA)25755Kuw/0,Tg(tetO-Ccnd1*T286A,-luc)11233Kuw/0	involves: 129S2/SvPas * FVB/N	N	22037875
MGI:5300589	M	MP:0001925	male infertility	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Tg(MMTVneu)202Mul/0	involves: 129S2/SvPas * FVB/N	N	22037875
MGI:5300589	M	MP:0001156	abnormal spermatogenesis	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Tg(MMTVneu)202Mul/0	involves: 129S2/SvPas * FVB/N	N	22037875
MGI:5300590	F	MP:0001382	abnormal nursing	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas * FVB/N	N	22037875
MGI:5301100	F	MP:0006269	abnormal mammary gland growth during pregnancy	Stat6<tm1Gru>/Stat6<tm1Gru>	involves: 129S2/SvPas * BALB/c	N	17611223
MGI:5301110	F	MP:0006269	abnormal mammary gland growth during pregnancy	Socs5<tm1Wsa>/Socs5<tm1Wsa>	involves: C57BL/6 * NZB	N	17611223
MGI:5301114	M	MP:0009451	abnormal chromosomal synapsis	X/Y(IsXPAR;Y)Ei	involves: LT/SvEi	N	1743079
MGI:5301171	M	MP:0003564	abnormal insulin secretion	Lepr<tm5Mgmj>/Lepr<tm5Mgmj>	B6.129-Lepr<tm5Mgmj>	N	24024119
MGI:5301171	F	MP:0001927	abnormal estrous cycle	Lepr<tm5Mgmj>/Lepr<tm5Mgmj>	B6.129-Lepr<tm5Mgmj>	N	MGI:5301120
MGI:5301171	M	MP:0005331	insulin resistance	Lepr<tm5Mgmj>/Lepr<tm5Mgmj>	B6.129-Lepr<tm5Mgmj>	N	24024119
MGI:5301319	M	MP:0001922	reduced male fertility	Mecom<tm1Aspe>/Mecom<tm1Aspe>	involves: 129S6/SvEvTac * C57BL/6	N	24316420
MGI:5301319	F	MP:0001923	reduced female fertility	Mecom<tm1Aspe>/Mecom<tm1Aspe>	involves: 129S6/SvEvTac * C57BL/6	N	24316420
MGI:5301527	F	MP:0009009	absent estrous cycle	Esr1<tm3.1Ksk>/Esr1<tm3.1Ksk>	involves: 129S6/SvEvTac * C57BL/6	N	21873215
MGI:5301527	F	MP:0001131	abnormal ovarian follicle morphology	Esr1<tm3.1Ksk>/Esr1<tm3.1Ksk>	involves: 129S6/SvEvTac * C57BL/6	N	21873215
MGI:5301527	F	MP:0000628	abnormal mammary gland development	Esr1<tm3.1Ksk>/Esr1<tm3.1Ksk>	involves: 129S6/SvEvTac * C57BL/6	N	21873215
MGI:5301527	F	MP:0001121	uterus hypoplasia	Esr1<tm3.1Ksk>/Esr1<tm3.1Ksk>	involves: 129S6/SvEvTac * C57BL/6	N	21873215
MGI:5301527	F	MP:0001134	absent corpus luteum	Esr1<tm3.1Ksk>/Esr1<tm3.1Ksk>	involves: 129S6/SvEvTac * C57BL/6	N	21873215
MGI:5301527	F	MP:0002637	small uterus	Esr1<tm3.1Ksk>/Esr1<tm3.1Ksk>	involves: 129S6/SvEvTac * C57BL/6	N	21873215
MGI:5301527	F	MP:0009096	decreased endometrial gland number	Esr1<tm3.1Ksk>/Esr1<tm3.1Ksk>	involves: 129S6/SvEvTac * C57BL/6	N	21873215
MGI:5301527	F	MP:0009082	uterus cyst	Esr1<tm3.1Ksk>/Esr1<tm3.1Ksk>	involves: 129S6/SvEvTac * C57BL/6	N	21873215
MGI:5301527	F	MP:0011121	decreased primordial ovarian follicle number	Esr1<tm3.1Ksk>/Esr1<tm3.1Ksk>	involves: 129S6/SvEvTac * C57BL/6	N	21873215
MGI:5301610	F	MP:0009222	increased uterus tumor incidence	Cop1<Gt(XR0653)1.1Wtsi>/Cop1<Gt(XR0653)1.1Wtsi>	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	21403399
MGI:5301610	M	MP:0004478	increased testicular teratoma incidence	Cop1<Gt(XR0653)1.1Wtsi>/Cop1<Gt(XR0653)1.1Wtsi>	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	21403399
MGI:5301866	F	MP:0009222	increased uterus tumor incidence	Fbxo4<tm1.1Jadi>/Fbxo4<+>	Not Specified	N	21911473
MGI:5301867	F	MP:0009222	increased uterus tumor incidence	Fbxo4<tm1.1Jadi>/Fbxo4<tm1.1Jadi>	Not Specified	N	21911473
MGI:5302224	M	MP:0002059	abnormal seminal vesicle morphology	Lzts2<tm1.1Zsu>/Lzts2<tm1.1Zsu>	B6.Cg-Lzts2<tm1.1Zsu>	N	21949185
MGI:5302224	F	MP:0009085	abnormal uterine horn morphology	Lzts2<tm1.1Zsu>/Lzts2<tm1.1Zsu>	B6.Cg-Lzts2<tm1.1Zsu>	N	21949185
MGI:5302224	M	MP:0013320	dilated seminal vesicle	Lzts2<tm1.1Zsu>/Lzts2<tm1.1Zsu>	B6.Cg-Lzts2<tm1.1Zsu>	N	21949185
MGI:5302385	F	MP:0001386	abnormal maternal nurturing	Cort<tm1Ldl>/Cort<tm1Ldl>	involves: C57BL/6J	N	21971153
MGI:5302532	F	MP:0005387	immune system phenotype	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	Y	21976681
MGI:5302540	F	MP:0004953	decreased spleen weight	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0005092	decreased double-positive T cell number	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0000706	small thymus	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0008088	abnormal T-helper 1 cell differentiation	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0005090	increased double-negative T cell number	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0004956	decreased thymus weight	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0000692	small spleen	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0004751	increased length of allograft survival	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0010221	abnormal T-helper 17 cell differentiation	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0001823	thymus hypoplasia	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0002398	abnormal bone marrow cell morphology/development	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0020913	increased susceptibility to Riboviria infection	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0002145	abnormal T cell differentiation	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0010136	decreased DN4 thymocyte number	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0005018	decreased T cell number	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0010133	increased DN3 thymocyte number	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0009541	increased thymocyte apoptosis	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302540	F	MP:0000694	spleen hypoplasia	Efnb1<tm1.1Jwu>/Efnb1<tm1.1Jwu>,Efnb2<tm1.1Jwu>/Efnb2<tm1.1Jwu>,Tg(Lck-cre)I540Jxm/0	B6.Cg-Efnb2<tm1.1Jwu> Efnb1<tm1.1Jwu> Tg(Lck-cre)I540Jxm	N	21976681
MGI:5302546	M	MP:0003461	abnormal response to novel object	Mecp2<tm1.1Meg>/Y	B6.129-Mecp2<tm1.1Meg>	N	21982370
MGI:5302546	M	MP:0008143	abnormal dendrite morphology	Mecp2<tm1.1Meg>/Y	B6.129-Mecp2<tm1.1Meg>	N	21982370
MGI:5302546	M	MP:0003107	abnormal response to novelty	Mecp2<tm1.1Meg>/Y	B6.129-Mecp2<tm1.1Meg>	N	21982370
MGI:5302546	M	MP:0005389	reproductive system phenotype	Mecp2<tm1.1Meg>/Y	B6.129-Mecp2<tm1.1Meg>	Y	21982370
MGI:5302546	M	MP:0014384	increased miniature inhibitory postsynaptic current amplitude	Mecp2<tm1.1Meg>/Y	B6.129-Mecp2<tm1.1Meg>	N	21982370
MGI:5302546	M	MP:0005386	behavior/neurological phenotype	Mecp2<tm1.1Meg>/Y	B6.129-Mecp2<tm1.1Meg>	Y	21982370
MGI:5302547	F	MP:0005389	reproductive system phenotype	Mecp2<tm1.1Meg>/Mecp2<tm1.1Meg>	B6.129-Mecp2<tm1.1Meg>	Y	21982370
MGI:5303089	M	MP:0001364	decreased anxiety-related response	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB	N	19016890
MGI:5303089	M	MP:0002761	abnormal hippocampal mossy fiber morphology	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB	N	11918288
MGI:5303089	M	MP:0001361	social withdrawal	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB	N	19016890
MGI:5303089	M	MP:0001363	increased anxiety-related response	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB	N	19016890
MGI:5303089	M	MP:0005391	vision/eye phenotype	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB	Y	19016890
MGI:5303089	M	MP:0005391	vision/eye phenotype	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB	Y	11918288
MGI:5303089	M	MP:0001415	increased exploration in new environment	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB	N	19016890
MGI:5303089	M	MP:0001260	increased body weight	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB	N	19016890
MGI:5303089	M	MP:0001405	impaired coordination	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB	N	19016890
MGI:5303089	M	MP:0000947	convulsive seizures	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB	N	11918288
MGI:5303089	M	MP:0003997	tonic-clonic seizures	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB	N	11918288
MGI:5303091	M	MP:0001364	decreased anxiety-related response	Fmr1<tm1Cgr>/Y	B6.129P2(FVB)-Fmr1<tm1Cgr>	N	19016890
MGI:5303091	M	MP:0005386	behavior/neurological phenotype	Fmr1<tm1Cgr>/Y	B6.129P2(FVB)-Fmr1<tm1Cgr>	Y	19016890
MGI:5303091	M	MP:0001361	social withdrawal	Fmr1<tm1Cgr>/Y	B6.129P2(FVB)-Fmr1<tm1Cgr>	N	19016890
MGI:5304170	F	MP:0031434	increased miscarriage rate	Tyr<c-47H>/Tyr<c-47H>	involves: 101/H * C3H/HeH	N	MGI:5303090
MGI:5304170	M	MP:0003642	absent seminal vesicle	Tyr<c-47H>/Tyr<c-47H>	involves: 101/H * C3H/HeH	N	MGI:5303090
MGI:5304170	M	MP:0001925	male infertility	Tyr<c-47H>/Tyr<c-47H>	involves: 101/H * C3H/HeH	N	MGI:5303090
MGI:5304184	M	MP:0005387	immune system phenotype	F8<tm1Kaz>/Y,Tg(Alb-F8*R593C)T4Mcal/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	Y	16493498
MGI:5305023	F	MP:0001274	curly vibrissae	Atp7a<Mo-18H>/Atp7a<+>	involves: 101/H	N	MGI:5304936
MGI:5305023	F	MP:0001284	absent vibrissae	Atp7a<Mo-18H>/Atp7a<+>	involves: 101/H	N	MGI:5304936
MGI:5305023	F	MP:0000421	mottled coat	Atp7a<Mo-18H>/Atp7a<+>	involves: 101/H	N	MGI:5304936
MGI:5305024	M	MP:0002080	prenatal lethality	Atp7a<Mo-18H>/Y	involves: 101/H	N	MGI:5304936
MGI:5305028	M	MP:0010233	hairless tail	Eda<Ta-27H>/Y	involves: 101/H * C3H/HeH	N	MGI:5304936
MGI:5305029	M	MP:0010233	hairless tail	Eda<Ta-28H>/Y	involves: 101/H	N	MGI:5304936
MGI:5305029	M	MP:0001302	eyelids open at birth	Eda<Ta-28H>/Y	involves: 101/H	N	MGI:5304936
MGI:5305031	M	MP:0003815	hairless	Eda<Ta-35H>/Y	involves: 101/H * C3H/HeH	N	MGI:5304936
MGI:5305031	M	MP:0010233	hairless tail	Eda<Ta-35H>/Y	involves: 101/H * C3H/HeH	N	MGI:5304936
MGI:5305032	M	MP:0003815	hairless	Eda<Ta-37H>/Y	involves: 101/H * C3H/HeH	N	MGI:5304936
MGI:5305032	M	MP:0010233	hairless tail	Eda<Ta-37H>/Y	involves: 101/H * C3H/HeH	N	MGI:5304936
MGI:5305033	M	MP:0000116	abnormal tooth development	Eda<Ta-38H>/Y	involves: 101/H * C3H/HeH	N	MGI:5304936
MGI:5305033	M	MP:0010233	hairless tail	Eda<Ta-38H>/Y	involves: 101/H * C3H/HeH	N	MGI:5304936
MGI:5305033	M	MP:0005176	eyelids fail to open	Eda<Ta-38H>/Y	involves: 101/H * C3H/HeH	N	MGI:5304936
MGI:5305283	F	MP:0002169	no abnormal phenotype detected	Irak1<tm1.1Pcoh>/Irak1<tm1.1Pcoh>	involves: 129P2/OlaHsd * C57BL/6	N	22007846
MGI:5305284	M	MP:0002169	no abnormal phenotype detected	Irak1<tm1.1Pcoh>/Y	involves: 129P2/OlaHsd * C57BL/6	N	22007846
MGI:5305722	M	MP:0008143	abnormal dendrite morphology	Arhgef6<tm1Kkut>/Y	B6.129-Arhgef6<tm1Kkut>	N	21989057
MGI:5305722	M	MP:0001473	reduced long-term potentiation	Arhgef6<tm1Kkut>/Y	B6.129-Arhgef6<tm1Kkut>	N	21989057
MGI:5305722	M	MP:0009936	abnormal dendritic spine morphology	Arhgef6<tm1Kkut>/Y	B6.129-Arhgef6<tm1Kkut>	N	21989057
MGI:5305722	M	MP:0009538	abnormal synapse morphology	Arhgef6<tm1Kkut>/Y	B6.129-Arhgef6<tm1Kkut>	N	21989057
MGI:5305722	M	MP:0001898	abnormal long-term depression	Arhgef6<tm1Kkut>/Y	B6.129-Arhgef6<tm1Kkut>	N	21989057
MGI:5305722	M	MP:0005386	behavior/neurological phenotype	Arhgef6<tm1Kkut>/Y	B6.129-Arhgef6<tm1Kkut>	Y	21989057
MGI:5305722	M	MP:0003461	abnormal response to novel object	Arhgef6<tm1Kkut>/Y	B6.129-Arhgef6<tm1Kkut>	N	21989057
MGI:5305722	M	MP:0001463	abnormal spatial learning	Arhgef6<tm1Kkut>/Y	B6.129-Arhgef6<tm1Kkut>	N	21989057
MGI:5305957	M	MP:0001925	male infertility	Tdrd7<tm1.1Chum>/Tdrd7<tm1.1Chum>	involves: 129S6/SvEvTac * C57BL/6	N	21670278
MGI:5305957	M	MP:0003698	abnormal male reproductive system physiology	Tdrd7<tm1.1Chum>/Tdrd7<tm1.1Chum>	involves: 129S6/SvEvTac * C57BL/6	N	21670278
MGI:5305957	M	MP:0001155	arrest of spermatogenesis	Tdrd7<tm1.1Chum>/Tdrd7<tm1.1Chum>	involves: 129S6/SvEvTac * C57BL/6	N	21670278
MGI:5305957	M	MP:0014052	increased male germ cell apoptosis	Tdrd7<tm1.1Chum>/Tdrd7<tm1.1Chum>	involves: 129S6/SvEvTac * C57BL/6	N	21670278
MGI:5305957	M	MP:0001147	small testis	Tdrd7<tm1.1Chum>/Tdrd7<tm1.1Chum>	involves: 129S6/SvEvTac * C57BL/6	N	21670278
MGI:5305958	M	MP:0001925	male infertility	Tdrd6<tm1Chum>/Tdrd6<tm1Chum>	involves: 129S4/SvJae * C57BL/6	N	21670278
MGI:5305958	M	MP:0001155	arrest of spermatogenesis	Tdrd6<tm1Chum>/Tdrd6<tm1Chum>	involves: 129S4/SvJae * C57BL/6	N	21670278
MGI:5305959	M	MP:0001925	male infertility	Tdrd6<tm1Chum>/Tdrd6<tm1Chum>,Tdrd7<tm1.1Chum>/Tdrd7<tm1.1Chum>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	21670278
MGI:5305959	M	MP:0001155	arrest of spermatogenesis	Tdrd6<tm1Chum>/Tdrd6<tm1Chum>,Tdrd7<tm1.1Chum>/Tdrd7<tm1.1Chum>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	21670278
MGI:5306141	M	MP:0004901	decreased male germ cell number	m1078Lja/m1078Lja	involves: C57BL/6J * DBA	N	22258617
MGI:5306141	M	MP:0001147	small testis	m1078Lja/m1078Lja	involves: C57BL/6J * DBA	N	22258617
MGI:5306142	M	MP:0004852	decreased testis weight	Snrpe<M1157Lja>/Snrpe<+>	involves: C57BL/6J * DBA	N	22258617
MGI:5306142	M	MP:0001156	abnormal spermatogenesis	Snrpe<M1157Lja>/Snrpe<+>	involves: C57BL/6J * DBA	N	22258617
MGI:5306143	M	MP:0001147	small testis	Prdm9<M1045Lja>/Prdm9<M1045Lja>	involves: C57BL/6J * DBA	N	22258617
MGI:5306143	M	MP:0004852	decreased testis weight	Prdm9<M1045Lja>/Prdm9<M1045Lja>	involves: C57BL/6J * DBA	N	22258617
MGI:5306143	M	MP:0005159	azoospermia	Prdm9<M1045Lja>/Prdm9<M1045Lja>	involves: C57BL/6J * DBA	N	22258617
MGI:5306145	M	MP:0004901	decreased male germ cell number	Prdm9<M1045Lja>/Prdm9<+>	involves: C57BL/6J * DBA	N	22258617
MGI:5306145	M	MP:0005159	azoospermia	Prdm9<M1045Lja>/Prdm9<+>	involves: C57BL/6J * DBA	N	22258617
MGI:5306145	M	MP:0001932	abnormal spermiogenesis	Prdm9<M1045Lja>/Prdm9<+>	involves: C57BL/6J * DBA	N	22258617
MGI:5306145	M	MP:0001147	small testis	Prdm9<M1045Lja>/Prdm9<+>	involves: C57BL/6J * DBA	N	22258617
MGI:5306145	M	MP:0006380	abnormal spermatid morphology	Prdm9<M1045Lja>/Prdm9<+>	involves: C57BL/6J * DBA	N	22258617
MGI:5306241	M	MP:0002804	abnormal motor learning	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	22119903
MGI:5306241	M	MP:0002083	premature death	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	16446138
MGI:5306241	M	MP:0001364	decreased anxiety-related response	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	22119903
MGI:5306241	M	MP:0008265	abnormal hippocampus CA2 region morphology	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	16446138
MGI:5306241	M	MP:0002175	decreased brain weight	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	16446138
MGI:5306241	M	MP:0001406	abnormal gait	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	22119903
MGI:5306241	M	MP:0004994	abnormal brain wave pattern	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	22119903
MGI:5306241	M	MP:0005202	lethargy	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	16446138
MGI:5306241	M	MP:0005402	abnormal action potential	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	16446138
MGI:5306241	M	MP:0001402	decreased locomotor activity	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	22119903
MGI:5306241	M	MP:0000819	abnormal olfactory bulb morphology	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	16446138
MGI:5306241	M	MP:0001405	impaired coordination	Mecp2<tm1.1Jae>/Y	involves: 129S4/SvJae * C57BL/6	N	22119903
MGI:5306255	M	MP:0005202	lethargy	Bdnf<tm3Jae>/Bdnf<tm3Jae>,Mecp2<tm1.1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * C57BL/6 * CBA/J	N	16446138
MGI:5306255	M	MP:0005402	abnormal action potential	Bdnf<tm3Jae>/Bdnf<tm3Jae>,Mecp2<tm1.1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * C57BL/6 * CBA/J	N	16446138
MGI:5306255	M	MP:0002083	premature death	Bdnf<tm3Jae>/Bdnf<tm3Jae>,Mecp2<tm1.1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * C57BL/6 * CBA/J	N	16446138
MGI:5306256	M	MP:0002083	premature death	Bdnf<tm3Jae>/Bdnf<+>,Mecp2<tm1.1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * C57BL/6 * CBA/J	N	16446138
MGI:5306257	M	MP:0002083	premature death	Col1a1<tm8(CAG-BDNF)Jae>/Col1a1<+>,Mecp2<tm1.1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * C57BL/6 * CBA/J	N	16446138
MGI:5306257	M	MP:0005386	behavior/neurological phenotype	Col1a1<tm8(CAG-BDNF)Jae>/Col1a1<+>,Mecp2<tm1.1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * C57BL/6 * CBA/J	Y	16446138
MGI:5306257	M	MP:0005402	abnormal action potential	Col1a1<tm8(CAG-BDNF)Jae>/Col1a1<+>,Mecp2<tm1.1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * C57BL/6 * CBA/J	N	16446138
MGI:5306257	M	MP:0002175	decreased brain weight	Col1a1<tm8(CAG-BDNF)Jae>/Col1a1<+>,Mecp2<tm1.1Jae>/Y,Tg(Camk2a-cre)93Kln/0	involves: 129S4/SvJae * C57BL/6 * CBA/J	N	16446138
MGI:5306957	M	MP:0001156	abnormal spermatogenesis	Sirt1<tm2.1Mcby>/Sirt1<tm2.1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22006156
MGI:5306957	M	MP:0020869	immotile sperm	Sirt1<tm2.1Mcby>/Sirt1<tm2.1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22006156
MGI:5306957	M	MP:0002687	oligozoospermia	Sirt1<tm2.1Mcby>/Sirt1<tm2.1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22006156
MGI:5306957	M	MP:0001925	male infertility	Sirt1<tm2.1Mcby>/Sirt1<tm2.1Mcby>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22006156
MGI:5306958	M	MP:0001925	male infertility	Sirt1<tm2.1Mcby>/Sirt1<tm2.1Mcby>	involves: 129S1/Sv * 129X1/SvJ	N	28273169
MGI:5307127	F	MP:0002495	increased IgA level	Was<tm1Sbs>/Was<tm1Sbs>	129S6/SvEvTac-Was<tm1Sbs>/J	N	22079330
MGI:5307127	F	MP:0011427	increased mesangial cell number	Was<tm1Sbs>/Was<tm1Sbs>	129S6/SvEvTac-Was<tm1Sbs>/J	N	22079330
MGI:5307127	F	MP:0011353	expanded mesangial matrix	Was<tm1Sbs>/Was<tm1Sbs>	129S6/SvEvTac-Was<tm1Sbs>/J	N	22079330
MGI:5307127	F	MP:0002962	increased urine protein level	Was<tm1Sbs>/Was<tm1Sbs>	129S6/SvEvTac-Was<tm1Sbs>/J	N	22079330
MGI:5307127	F	MP:0020519	renal glomerular immunoglobulin deposits	Was<tm1Sbs>/Was<tm1Sbs>	129S6/SvEvTac-Was<tm1Sbs>/J	N	22079330
MGI:5307127	F	MP:0002743	glomerulonephritis	Was<tm1Sbs>/Was<tm1Sbs>	129S6/SvEvTac-Was<tm1Sbs>/J	N	22079330
MGI:5307127	F	MP:0011339	abnormal glomerular mesangium morphology	Was<tm1Sbs>/Was<tm1Sbs>	129S6/SvEvTac-Was<tm1Sbs>/J	N	22079330
MGI:5307127	F	MP:0002135	abnormal kidney morphology	Was<tm1Sbs>/Was<tm1Sbs>	129S6/SvEvTac-Was<tm1Sbs>/J	N	22079330
MGI:5307127	F	MP:0002494	increased IgM level	Was<tm1Sbs>/Was<tm1Sbs>	129S6/SvEvTac-Was<tm1Sbs>/J	N	22079330
MGI:5307261	M	MP:0009404	centrally nucleated skeletal muscle fibers	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0001406	abnormal gait	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0009400	decreased skeletal muscle fiber size	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0005659	decreased susceptibility to diet-induced obesity	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0001544	abnormal cardiovascular system physiology	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0000748	progressive muscle weakness	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0009417	skeletal muscle atrophy	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0009422	decreased gastrocnemius weight	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0009428	decreased tibialis anterior weight	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0001262	decreased body weight	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0005386	behavior/neurological phenotype	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	Y	22068590
MGI:5307261	M	MP:0002133	abnormal respiratory system physiology	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0003082	abnormal gastrocnemius morphology	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0004819	decreased skeletal muscle mass	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0002083	premature death	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0005370	liver/biliary system phenotype	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	Y	22068590
MGI:5307261	M	MP:0001954	respiratory distress	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0001529	abnormal vocalization	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0005388	respiratory system phenotype	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	Y	22068590
MGI:5307261	M	MP:0010227	decreased quadriceps weight	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0005389	reproductive system phenotype	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	Y	22068590
MGI:5307261	M	MP:0001922	reduced male fertility	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5307261	M	MP:0009403	increased variability of skeletal muscle fiber size	Mtm1<tm1Itl>/Y	B6.Cg-Mtm1<tm1Itl>	N	22068590
MGI:5308127	M	MP:0001922	reduced male fertility	Tg(Prnp-AR*112Q)#Deme/0	involves: C57BL/6 * SJL	N	15152038
MGI:5308361	M	MP:0006380	abnormal spermatid morphology	Tsc22d3<tm1.1Ric>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	22110132
MGI:5308361	M	MP:0008261	arrest of male meiosis	Tsc22d3<tm1.1Ric>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	22110132
MGI:5308361	M	MP:0002685	abnormal spermatogonia proliferation	Tsc22d3<tm1.1Ric>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	22110132
MGI:5308361	M	MP:0001925	male infertility	Tsc22d3<tm1.1Ric>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	22110132
MGI:5308361	M	MP:0001156	abnormal spermatogenesis	Tsc22d3<tm1.1Ric>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	22110132
MGI:5308361	M	MP:0005159	azoospermia	Tsc22d3<tm1.1Ric>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	22110132
MGI:5308361	M	MP:0004849	abnormal testis size	Tsc22d3<tm1.1Ric>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	22110132
MGI:5308361	M	MP:0004901	decreased male germ cell number	Tsc22d3<tm1.1Ric>/Y	involves: 129S7/SvEvBrd * C57BL/6	N	22110132
MGI:5308362	M	MP:0001156	abnormal spermatogenesis	Tsc22d3<tm1Ric>/Y,Tg(Ddx4-cre)1Dcas/?	involves: C57BL/6 * FVB	N	22110132
MGI:5308362	M	MP:0001925	male infertility	Tsc22d3<tm1Ric>/Y,Tg(Ddx4-cre)1Dcas/?	involves: C57BL/6 * FVB	N	22110132
MGI:5308362	M	MP:0006380	abnormal spermatid morphology	Tsc22d3<tm1Ric>/Y,Tg(Ddx4-cre)1Dcas/?	involves: C57BL/6 * FVB	N	22110132
MGI:5308362	M	MP:0004901	decreased male germ cell number	Tsc22d3<tm1Ric>/Y,Tg(Ddx4-cre)1Dcas/?	involves: C57BL/6 * FVB	N	22110132
MGI:5308362	M	MP:0005159	azoospermia	Tsc22d3<tm1Ric>/Y,Tg(Ddx4-cre)1Dcas/?	involves: C57BL/6 * FVB	N	22110132
MGI:5308362	M	MP:0004849	abnormal testis size	Tsc22d3<tm1Ric>/Y,Tg(Ddx4-cre)1Dcas/?	involves: C57BL/6 * FVB	N	22110132
MGI:5308362	M	MP:0008261	arrest of male meiosis	Tsc22d3<tm1Ric>/Y,Tg(Ddx4-cre)1Dcas/?	involves: C57BL/6 * FVB	N	22110132
MGI:5308720	M	MP:0006380	abnormal spermatid morphology	Hspa4<tm1Imad>/Hspa4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21487003
MGI:5308720	M	MP:0001156	abnormal spermatogenesis	Hspa4<tm1Imad>/Hspa4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21487003
MGI:5308720	M	MP:0001153	small seminiferous tubules	Hspa4<tm1Imad>/Hspa4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21487003
MGI:5308720	M	MP:0002687	oligozoospermia	Hspa4<tm1Imad>/Hspa4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21487003
MGI:5308720	M	MP:0008261	arrest of male meiosis	Hspa4<tm1Imad>/Hspa4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21487003
MGI:5308720	M	MP:0014052	increased male germ cell apoptosis	Hspa4<tm1Imad>/Hspa4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21487003
MGI:5308720	M	MP:0004852	decreased testis weight	Hspa4<tm1Imad>/Hspa4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21487003
MGI:5308720	M	MP:0006379	abnormal spermatocyte morphology	Hspa4<tm1Imad>/Hspa4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21487003
MGI:5308720	M	MP:0001925	male infertility	Hspa4<tm1Imad>/Hspa4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21487003
MGI:5308720	M	MP:0002675	asthenozoospermia	Hspa4<tm1Imad>/Hspa4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21487003
MGI:5308720	M	MP:0002216	abnormal seminiferous tubule morphology	Hspa4<tm1Imad>/Hspa4<tm1Imad>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21487003
MGI:5308721	M	MP:0001925	male infertility	Bgn<tm1Mfy>/Y,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	21502335
MGI:5308721	M	MP:0008151	increased diameter of long bones	Bgn<tm1Mfy>/Y,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308721	M	MP:0011642	abnormal bone collagen fibril morphology	Bgn<tm1Mfy>/Y,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308721	M	MP:0010962	decreased compact bone mass	Bgn<tm1Mfy>/Y,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308721	M	MP:0003089	decreased skin tensile strength	Bgn<tm1Mfy>/Y,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308721	M	MP:0010873	decreased trabecular bone mass	Bgn<tm1Mfy>/Y,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308721	M	MP:0004686	decreased length of long bones	Bgn<tm1Mfy>/Y,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308721	M	MP:0000063	decreased bone mineral density	Bgn<tm1Mfy>/Y,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308721	M	MP:0004126	thin hypodermis	Bgn<tm1Mfy>/Y,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308721	M	MP:0001244	thin dermal layer	Bgn<tm1Mfy>/Y,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308721	M	MP:0008438	abnormal cutaneous collagen fibril morphology	Bgn<tm1Mfy>/Y,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308722	F	MP:0001262	decreased body weight	Bgn<tm1Mfy>/Bgn<tm1Mfy>,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	21502335
MGI:5308722	F	MP:0001923	reduced female fertility	Bgn<tm1Mfy>/Bgn<tm1Mfy>,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	21502335
MGI:5308722	F	MP:0001935	decreased litter size	Bgn<tm1Mfy>/Bgn<tm1Mfy>,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	21502335
MGI:5308722	F	MP:0002081	perinatal lethality	Bgn<tm1Mfy>/Bgn<tm1Mfy>,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	21502335
MGI:5308722	F	MP:0002294	short gestation period	Bgn<tm1Mfy>/Bgn<tm1Mfy>,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	21502335
MGI:5308722	F	MP:0012009	early parturition	Bgn<tm1Mfy>/Bgn<tm1Mfy>,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	21502335
MGI:5308723	F	MP:0012009	early parturition	Bgn<tm1Mfy>/Bgn<+>,Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	21502335
MGI:5308724	F	MP:0012008	delayed parturition	Bgn<tm1Mfy>/Bgn<tm1Mfy>,Dcn<tm1Ioz>/Dcn<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	21502335
MGI:5308725	F	MP:0001923	reduced female fertility	Dcn<tm1Ioz>/Dcn<tm1Ioz>	involves: 129S1/Sv * 129X1/SvJ	N	21502335
MGI:5308726	M	MP:0008438	abnormal cutaneous collagen fibril morphology	Bgn<tm1Mfy>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308726	M	MP:0001244	thin dermal layer	Bgn<tm1Mfy>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308726	M	MP:0011643	abnormal tendon collagen fibril morphology	Bgn<tm1Mfy>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308726	M	MP:0011642	abnormal bone collagen fibril morphology	Bgn<tm1Mfy>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	12102052
MGI:5308726	M	MP:0010771	integument phenotype	Bgn<tm1Mfy>/Y	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	Y	12102052
MGI:5308736	F	MP:0001126	abnormal ovary morphology	Becn1<tm1.1Ebr>/Becn1<+>	Not Specified	N	21464117
MGI:5308737	F	MP:0009361	abnormal primordial ovarian follicle morphology	Becn1<tm1Ebr>/Becn1<+>,Tg(MMTV-cre)1Mam/?	involves: FVB	N	21464117
MGI:5308737	F	MP:0011121	decreased primordial ovarian follicle number	Becn1<tm1Ebr>/Becn1<+>,Tg(MMTV-cre)1Mam/?	involves: FVB	N	21464117
MGI:5308737	F	MP:0001127	small ovary	Becn1<tm1Ebr>/Becn1<+>,Tg(MMTV-cre)1Mam/?	involves: FVB	N	21464117
MGI:5308754	F	MP:0004833	ovary atrophy	Mcph1<tm1.1Zqw>/Mcph1<tm1.1Zqw>	Not Specified	N	21947081
MGI:5308754	M	MP:0003205	testicular atrophy	Mcph1<tm1.1Zqw>/Mcph1<tm1.1Zqw>	Not Specified	N	21947081
MGI:5310735	M	MP:0001406	abnormal gait	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0001364	decreased anxiety-related response	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0002690	akinesia	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0004924	abnormal behavior	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0001405	impaired coordination	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0002083	premature death	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0002064	seizures	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0009454	impaired contextual conditioning behavior	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0001402	decreased locomotor activity	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0009456	impaired cued conditioning behavior	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0001262	decreased body weight	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0002804	abnormal motor learning	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0001513	limb grasping	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0002175	decreased brain weight	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310735	M	MP:0004994	abnormal brain wave pattern	Mecp2<tm1.1Joez>/Y	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310737	M	MP:0009940	abnormal hippocampus pyramidal cell morphology	Mecp2<tm1.1Joez>/Y,Tg(Thy1-EGFP)#Jrs/0	involves: 129 * C57BL/6 * C57BL/6J * CBA	N	22119903
MGI:5310738	F	MP:0004924	abnormal behavior	Mecp2<tm1.1Joez>/Mecp2<+>	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310738	F	MP:0001402	decreased locomotor activity	Mecp2<tm1.1Joez>/Mecp2<+>	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310738	F	MP:0001260	increased body weight	Mecp2<tm1.1Joez>/Mecp2<+>	B6.129-Mecp2<tm1.1Joez>	N	22119903
MGI:5310738	F	MP:0010768	mortality/aging	Mecp2<tm1.1Joez>/Mecp2<+>	B6.129-Mecp2<tm1.1Joez>	Y	22119903
MGI:5310739	M	MP:0010768	mortality/aging	Mecp2<tm2.1Joez>/Y	B6.129-Mecp2<tm2.1Joez>	Y	22119903
MGI:5310739	M	MP:0005378	growth/size/body region phenotype	Mecp2<tm2.1Joez>/Y	B6.129-Mecp2<tm2.1Joez>	Y	22119903
MGI:5310739	M	MP:0003631	nervous system phenotype	Mecp2<tm2.1Joez>/Y	B6.129-Mecp2<tm2.1Joez>	Y	22119903
MGI:5310746	F	MP:0005389	reproductive system phenotype	H2<d>/H2<d>,Trap1a<tm1.1Jvde>/Trap1a<tm1.1Jvde>	involves: 129 * BALB/cJ * C57BL/10 * DBA/2	Y	22140254
MGI:5310747	M	MP:0005000	abnormal immune tolerance	H2<d>/H2<d>,Trap1a<tm1.1Jvde>/Y	involves: 129 * BALB/cJ * C57BL/10 * DBA/2	N	22140254
MGI:5310747	M	MP:0005389	reproductive system phenotype	H2<d>/H2<d>,Trap1a<tm1.1Jvde>/Y	involves: 129 * BALB/cJ * C57BL/10 * DBA/2	Y	22140254
MGI:5310747	M	MP:0010537	tumor regression	H2<d>/H2<d>,Trap1a<tm1.1Jvde>/Y	involves: 129 * BALB/cJ * C57BL/10 * DBA/2	N	22140254
MGI:5310747	M	MP:0009764	decreased susceptibility to induced morbidity/mortality	H2<d>/H2<d>,Trap1a<tm1.1Jvde>/Y	involves: 129 * BALB/cJ * C57BL/10 * DBA/2	N	22140254
MGI:5310747	M	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology	H2<d>/H2<d>,Trap1a<tm1.1Jvde>/Y	involves: 129 * BALB/cJ * C57BL/10 * DBA/2	N	22140254
MGI:5310748	M	MP:0005002	abnormal T cell clonal deletion	H2<d>/H2<d>,Tg(TcraP1.5,TcrbP1.5)29Amsv/0,Trap1a<tm1.1Jvde>/Y	involves: 129 * BALB/cJ * C57BL/10 * DBA/2	N	22140254
MGI:5310750	M	MP:0008545	absent sperm flagellum	Arl6<tm2Vcs>/Arl6<tm2Vcs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22139371
MGI:5310750	M	MP:0001925	male infertility	Arl6<tm2Vcs>/Arl6<tm2Vcs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22139371
MGI:5310976	M	MP:0001925	male infertility	Nsun2<Gt(D014D11)Wrst>/Nsun2<Gt(D014D11)Wrst>	involves: 129S2/SvPas * C57BL/6J * CBA	N	22144916
MGI:5310977	M	MP:0001925	male infertility	Nsun2<tm1a(EUCOMM)Wtsi>/Nsun2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	22144916
MGI:5311889	M	MP:0003415	priapism	Chy6/Chy6<+>	involves: C3H/HeH	N	12644183
MGI:5313315	F	MP:0001923	reduced female fertility	Ufde/Ufde<+>	involves: C3H/HeH	N	MGI:4940633
MGI:5313412	F	MP:0000749	muscle degeneration	Dmd<mdx>/Dmd<mdx>,Mamstr<tm1.2Eno>/Mamstr<tm1.2Eno>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22279050
MGI:5313412	F	MP:0010239	decreased skeletal muscle weight	Dmd<mdx>/Dmd<mdx>,Mamstr<tm1.2Eno>/Mamstr<tm1.2Eno>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22279050
MGI:5313412	F	MP:0001262	decreased body weight	Dmd<mdx>/Dmd<mdx>,Mamstr<tm1.2Eno>/Mamstr<tm1.2Eno>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22279050
MGI:5313412	F	MP:0009419	skeletal muscle fibrosis	Dmd<mdx>/Dmd<mdx>,Mamstr<tm1.2Eno>/Mamstr<tm1.2Eno>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22279050
MGI:5313412	F	MP:0009410	abnormal skeletal muscle satellite cell proliferation	Dmd<mdx>/Dmd<mdx>,Mamstr<tm1.2Eno>/Mamstr<tm1.2Eno>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22279050
MGI:5313433	M	MP:0005385	cardiovascular system phenotype	Vamp7<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6	Y	22323709
MGI:5313433	M	MP:0003443	increased circulating glycerol level	Vamp7<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6	N	22323709
MGI:5313433	M	MP:0002175	decreased brain weight	Vamp7<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6	N	22323709
MGI:5313433	M	MP:0005534	decreased body temperature	Vamp7<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6	N	22323709
MGI:5313433	M	MP:0001363	increased anxiety-related response	Vamp7<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6	N	22323709
MGI:5313499	F	MP:0008450	retina photoreceptor degeneration	Tg(CAG-Rpgr)mRDefWrght/0,Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6J	N	21546531
MGI:5313499	F	MP:0008587	short photoreceptor outer segment	Tg(CAG-Rpgr)mRDefWrght/0,Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6J	N	21546531
MGI:5313499	F	MP:0008582	short photoreceptor inner segment	Tg(CAG-Rpgr)mRDefWrght/0,Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6J	N	21546531
MGI:5313499	F	MP:0003731	abnormal retina outer nuclear layer morphology	Tg(CAG-Rpgr)mRDefWrght/0,Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6J	N	21546531
MGI:5313499	F	MP:0001006	abnormal retina cone cell morphology	Tg(CAG-Rpgr)mRDefWrght/0,Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6J	N	21546531
MGI:5313499	F	MP:0008586	disorganized photoreceptor outer segment	Tg(CAG-Rpgr)mRDefWrght/0,Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6J	N	21546531
MGI:5313504	F	MP:0005391	vision/eye phenotype	Tg(CAG-Rpgr)mROrfWrght/0,Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6J	Y	21546531
MGI:5313506	F	MP:0008450	retina photoreceptor degeneration	Tg(CAG-Rpgr)mROrfWrght/0,Tg(CAG-Rpgr)mRDefWrght/0,Rpgr<tm1Tili>/Rpgr<tm1Tili>	involves: 129S4/SvJae * C57BL/6J	N	21546531
MGI:5313545	F	MP:0011644	abnormal oviduct epithelium motile cilium morphology	Odf2<tm1.1Sats>/Odf2<tm1.2Sats>,Tg(CAG-cre)13Miya/0	involves: C57BL/6 * C57BL/6J	N	22265411
MGI:5313546	M	MP:0001925	male infertility	Odf2<tm1.2Sats>/Odf2<+>	involves: C57BL/6 * C57BL/6J	N	22265411
MGI:5313804	F	MP:0006269	abnormal mammary gland growth during pregnancy	Tg(Wap-TAg)12Gmn/?	involves: NMRI	N	11402328
MGI:5313804	F	MP:0010249	lactation failure	Tg(Wap-TAg)12Gmn/?	involves: NMRI	N	11402328
MGI:5313804	F	MP:0006270	abnormal mammary gland growth during lactation	Tg(Wap-TAg)12Gmn/?	involves: NMRI	N	11402328
MGI:5313804	F	MP:0009504	abnormal mammary gland epithelium morphology	Tg(Wap-TAg)12Gmn/?	involves: NMRI	N	11402328
MGI:5313815	M	MP:0001922	reduced male fertility	Cntnap1<shm-5J>/Cntnap1<shm-5J>	B6.Cg-Cntnap1<shm-5J>/GrsrJ	N	MGI:5313513
MGI:5313816	F	MP:0009504	abnormal mammary gland epithelium morphology	Tg(Wap-tAg)1Gmn/?	involves: NMRI	N	11402328
MGI:5313816	F	MP:0010249	lactation failure	Tg(Wap-tAg)1Gmn/?	involves: NMRI	N	11402328
MGI:5313816	F	MP:0009503	abnormal mammary gland duct morphology	Tg(Wap-tAg)1Gmn/?	involves: NMRI	N	11402328
MGI:5313816	F	MP:0006269	abnormal mammary gland growth during pregnancy	Tg(Wap-tAg)1Gmn/?	involves: NMRI	N	11402328
MGI:5313816	F	MP:0009506	abnormal mammary gland alveolus morphology	Tg(Wap-tAg)1Gmn/?	involves: NMRI	N	11402328
MGI:5314391	F	MP:0005293	impaired glucose tolerance	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0002078	abnormal glucose homeostasis	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0010024	increased total body fat amount	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0002079	increased circulating insulin level	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0014172	decreased fatty acid oxidation	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0001433	polyphagia	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0009286	increased abdominal fat pad weight	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0003960	increased lean body mass	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0031415	increased skeletal muscle triglyceride level	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0001261	obese	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0030022	decreased muscle cell glucose uptake	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0005331	insulin resistance	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0004890	decreased energy expenditure	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0008964	decreased carbon dioxide production	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0002644	decreased circulating triglyceride level	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0010379	decreased respiratory quotient	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0005669	increased circulating leptin level	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0003058	increased insulin secretion	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	M	MP:0005378	growth/size/body region phenotype	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	Y	20381490
MGI:5314391	F	MP:0005438	abnormal glycogen homeostasis	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314391	F	MP:0005290	decreased oxygen consumption	Ceacam2<tm1Snaj>/Ceacam2<tm1Snaj>	involves: 129S4/SvJae * C57BL/6	N	20381490
MGI:5314543	F	MP:0000267	abnormal heart development	Hprt1<tm2(CAG-TBX2,-EGFP)Akis>/Hprt1<+>,Tg(Myh6-cre)2182Mds/0	involves: 129 * FVB/N * NMRI	N	22130515
MGI:5314904	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Huwe1<tm1.2Mak>/Y	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6 * SJL	N	22213803
MGI:5314904	M	MP:0011732	decreased somite size	Huwe1<tm1.2Mak>/Y	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6 * SJL	N	22213803
MGI:5314904	M	MP:0001698	decreased embryo size	Huwe1<tm1.2Mak>/Y	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6 * SJL	N	22213803
MGI:5314904	M	MP:0000274	enlarged heart	Huwe1<tm1.2Mak>/Y	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6 * SJL	N	22213803
MGI:5314905	M	MP:0008495	decreased IgG1 level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0004816	abnormal class switch recombination	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0005093	decreased B cell proliferation	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0008174	decreased follicular B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0001807	decreased IgA level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0001800	abnormal humoral immune response	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0020913	increased susceptibility to Riboviria infection	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0008182	decreased marginal zone B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0008209	decreased pre-B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0002144	abnormal B cell differentiation	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0008496	decreased IgG2a level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0008203	absent B-1a cells	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0001806	decreased IgM level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0008498	decreased IgG3 level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0008782	increased B cell apoptosis	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0008211	decreased mature B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314905	M	MP:0008190	decreased transitional stage B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y	B6.Cg-Cd79a<tm1(cre)Reth> Huwe1<tm1.1Mak>	N	22213803
MGI:5314906	M	MP:0001806	decreased IgM level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	22213803
MGI:5314906	M	MP:0005387	immune system phenotype	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6 * SJL	Y	22213803
MGI:5314906	M	MP:0008203	absent B-1a cells	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	22213803
MGI:5314906	M	MP:0008495	decreased IgG1 level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	22213803
MGI:5314906	M	MP:0004816	abnormal class switch recombination	Cd79a<tm1(cre)Reth>/Cd79a<+>,Huwe1<tm1.1Mak>/Y,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	22213803
MGI:5314953	M	MP:0001925	male infertility	Eif4h<Gt(Ex279)Byg>/Eif4h<Gt(Ex279)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22234171
MGI:5314953	F	MP:0001923	reduced female fertility	Eif4h<Gt(Ex279)Byg>/Eif4h<Gt(Ex279)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22234171
MGI:5315472	M	MP:0004852	decreased testis weight	Spata22<repro42>/Spata22<repro42>	involves: C3HeB/FeJ * C57BL/6J	N	22011390
MGI:5315472	F	MP:0004805	absent oocytes	Spata22<repro42>/Spata22<repro42>	involves: C3HeB/FeJ * C57BL/6J	N	22011390
MGI:5315472	M	MP:0006380	abnormal spermatid morphology	Spata22<repro42>/Spata22<repro42>	involves: C3HeB/FeJ * C57BL/6J	N	22011390
MGI:5315472	M	MP:0006379	abnormal spermatocyte morphology	Spata22<repro42>/Spata22<repro42>	involves: C3HeB/FeJ * C57BL/6J	N	22011390
MGI:5315472	F	MP:0001127	small ovary	Spata22<repro42>/Spata22<repro42>	involves: C3HeB/FeJ * C57BL/6J	N	22011390
MGI:5315472	M	MP:0001155	arrest of spermatogenesis	Spata22<repro42>/Spata22<repro42>	involves: C3HeB/FeJ * C57BL/6J	N	22011390
MGI:5315472	M	MP:0005159	azoospermia	Spata22<repro42>/Spata22<repro42>	involves: C3HeB/FeJ * C57BL/6J	N	22011390
MGI:5315472	F	MP:0002016	ovary cyst	Spata22<repro42>/Spata22<repro42>	involves: C3HeB/FeJ * C57BL/6J	N	22011390
MGI:5315472	F	MP:0005168	abnormal female meiosis	Spata22<repro42>/Spata22<repro42>	involves: C3HeB/FeJ * C57BL/6J	N	22011390
MGI:5315472	M	MP:0008261	arrest of male meiosis	Spata22<repro42>/Spata22<repro42>	involves: C3HeB/FeJ * C57BL/6J	N	22011390
MGI:5315472	F	MP:0001131	abnormal ovarian follicle morphology	Spata22<repro42>/Spata22<repro42>	involves: C3HeB/FeJ * C57BL/6J	N	22011390
MGI:5315472	F	MP:0001926	female infertility	Spata22<repro42>/Spata22<repro42>	involves: C3HeB/FeJ * C57BL/6J	N	22011390
MGI:5315472	M	MP:0001925	male infertility	Spata22<repro42>/Spata22<repro42>	involves: C3HeB/FeJ * C57BL/6J	N	22011390
MGI:5315707	M	MP:0001925	male infertility	Cdo1<tm1.1Mhst>/Cdo1<tm1.1Mhst>	involves: C57BL/6	N	21693692
MGI:5315741	F	MP:0010768	mortality/aging	Mir188<tm1.1Mtm>/Mir188<tm1.1Mtm>	involves: 129P2/OlaHsd * C57BL/6 * FVB	Y	MGI:5314248
MGI:5315744	F	MP:0010768	mortality/aging	Mir322<tm1.1Mtm>/Mir322<tm1.1Mtm>	involves: 129P2/OlaHsd * C57BL/6 * FVB	Y	MGI:5314248
MGI:5315771	M	MP:0009282	decreased hyperactivated sperm motility	Catsperd<tm1.1Clph>/Catsperd<tm1.1Clph>	involves: 129S4/SvJae * C57BL/6	N	21224844
MGI:5315771	M	MP:0001925	male infertility	Catsperd<tm1.1Clph>/Catsperd<tm1.1Clph>	involves: 129S4/SvJae * C57BL/6	N	21224844
MGI:5315771	M	MP:0005578	teratozoospermia	Catsperd<tm1.1Clph>/Catsperd<tm1.1Clph>	involves: 129S4/SvJae * C57BL/6	N	21224844
MGI:5315771	M	MP:0002687	oligozoospermia	Catsperd<tm1.1Clph>/Catsperd<tm1.1Clph>	involves: 129S4/SvJae * C57BL/6	N	21224844
MGI:5315849	F	MP:0002169	no abnormal phenotype detected	Huwe1<tm1Wgu>/Huwe1<tm1Wgu>	involves: C57BL/6J	N	22187431
MGI:5315850	M	MP:0002169	no abnormal phenotype detected	Huwe1<tm1Wgu>/Y	involves: C57BL/6J	N	22187431
MGI:5315852	M	MP:0002727	decreased circulating insulin level	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * CBA/J	N	22187431
MGI:5315852	M	MP:0000538	abnormal urinary bladder morphology	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * CBA/J	N	22187431
MGI:5315852	M	MP:0002083	premature death	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * CBA/J	N	22187431
MGI:5315852	M	MP:0005559	increased circulating glucose level	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * CBA/J	N	22187431
MGI:5315852	M	MP:0005293	impaired glucose tolerance	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * CBA/J	N	22187431
MGI:5315852	M	MP:0001762	polyuria	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * CBA/J	N	22187431
MGI:5315852	M	MP:0009254	disorganized pancreatic islets	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * CBA/J	N	22187431
MGI:5315852	M	MP:0001559	hyperglycemia	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * CBA/J	N	22187431
MGI:5315852	M	MP:0003339	decreased pancreatic beta cell number	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * CBA/J	N	22187431
MGI:5315852	M	MP:0001262	decreased body weight	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * CBA/J	N	22187431
MGI:5315853	M	MP:0010768	mortality/aging	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0,Trp53<tm1Thl>/Trp53<tm1Thl>	involves: C57BL/6J * CBA/J	Y	22187431
MGI:5315853	M	MP:0005376	homeostasis/metabolism phenotype	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0,Trp53<tm1Thl>/Trp53<tm1Thl>	involves: C57BL/6J * CBA/J	Y	22187431
MGI:5315853	M	MP:0001559	hyperglycemia	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0,Trp53<tm1Thl>/Trp53<tm1Thl>	involves: C57BL/6J * CBA/J	N	22187431
MGI:5315853	M	MP:0005379	endocrine/exocrine gland phenotype	Huwe1<tm1Wgu>/Y,Tg(Ins2-cre)23Herr/0,Trp53<tm1Thl>/Trp53<tm1Thl>	involves: C57BL/6J * CBA/J	Y	22187431
MGI:5316007	F	MP:0001844	autoimmune response	Gata1<tm6Sho>/Gata1<tm6Sho>	C.129S1-Gata1<tm6Sho>	N	22416124
MGI:5316007	F	MP:0005501	abnormal skin physiology	Gata1<tm6Sho>/Gata1<tm6Sho>	C.129S1-Gata1<tm6Sho>	N	22416124
MGI:5316009	F	MP:0005387	immune system phenotype	Cysltr1<tm1Ykn>/Cysltr1<tm1Ykn>	C.B6-Cysltr1<tm1Ykn>	Y	22416124
MGI:5316043	M	MP:0001489	decreased startle reflex	Fmr1<tm1Cgr>/Y	FVB.129P2(B6)-Fmr1<tm1Cgr>/J	N	16887106
MGI:5316044	M	MP:0001925	male infertility	T(7;19)145H/?	involves: 101/H * C3H/HeH	N	5958877
MGI:5316044	F	MP:0001923	reduced female fertility	T(7;19)145H/?	involves: 101/H * C3H/HeH	N	5958877
MGI:5316044	M	MP:0005159	azoospermia	T(7;19)145H/?	involves: 101/H * C3H/HeH	N	5958877
MGI:5316044	M	MP:0004852	decreased testis weight	T(7;19)145H/?	involves: 101/H * C3H/HeH	N	5958877
MGI:5316044	M	MP:0008261	arrest of male meiosis	T(7;19)145H/?	involves: 101/H * C3H/HeH	N	5958877
MGI:5316077	M	MP:0005391	vision/eye phenotype	Fmr1<tm1Cgr>/Y	FVB.129P2(B6)-Pde6b<+> Fmr1<tm1Cgr>	Y	16093389
MGI:5316077	M	MP:0002062	abnormal associative learning	Fmr1<tm1Cgr>/Y	FVB.129P2(B6)-Pde6b<+> Fmr1<tm1Cgr>	N	16093389
MGI:5316077	M	MP:0009456	impaired cued conditioning behavior	Fmr1<tm1Cgr>/Y	FVB.129P2(B6)-Pde6b<+> Fmr1<tm1Cgr>	N	16093389
MGI:5316077	M	MP:0001473	reduced long-term potentiation	Fmr1<tm1Cgr>/Y	FVB.129P2(B6)-Pde6b<+> Fmr1<tm1Cgr>	N	16093389
MGI:5316080	M	MP:0001496	audiogenic seizures	Fmr1<tm1Cgr>/Y	either: FVB.129P2(B6)-Fmr1<tm1Cgr>/J or FVB;129P2(B6)-Fmr1<tm1Cgr>/J	N	11301211
MGI:5316080	M	MP:0009141	increased prepulse inhibition	Fmr1<tm1Cgr>/Y	either: FVB.129P2(B6)-Fmr1<tm1Cgr>/J or FVB;129P2(B6)-Fmr1<tm1Cgr>/J	N	11301211
MGI:5316080	M	MP:0001489	decreased startle reflex	Fmr1<tm1Cgr>/Y	either: FVB.129P2(B6)-Fmr1<tm1Cgr>/J or FVB;129P2(B6)-Fmr1<tm1Cgr>/J	N	11301211
MGI:5316368	M	MP:0005386	behavior/neurological phenotype	Pdilt<tm1Osb>/Pdilt<tm1Osb>	involves: 129S2/SvPas	Y	22357757
MGI:5316368	M	MP:0004543	abnormal sperm physiology	Pdilt<tm1Osb>/Pdilt<tm1Osb>	involves: 129S2/SvPas	N	22357757
MGI:5316368	M	MP:0001925	male infertility	Pdilt<tm1Osb>/Pdilt<tm1Osb>	involves: 129S2/SvPas	N	22357757
MGI:5316368	M	MP:0031012	impaired sperm migration in female genital tract	Pdilt<tm1Osb>/Pdilt<tm1Osb>	involves: 129S2/SvPas	N	22357757
MGI:5316368	M	MP:0005389	reproductive system phenotype	Pdilt<tm1Osb>/Pdilt<tm1Osb>	involves: 129S2/SvPas	Y	22357757
MGI:5316380	M	MP:0014052	increased male germ cell apoptosis	Pum1<tm1.1Hfl>/Pum1<tm1.2Hfl>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6 * FVB	N	22342750
MGI:5316381	M	MP:0002687	oligozoospermia	Pum1<tm1.2Hfl>/Pum1<+>	involves: 129 * C57BL/6 * FVB	N	22342750
MGI:5316381	M	MP:0014052	increased male germ cell apoptosis	Pum1<tm1.2Hfl>/Pum1<+>	involves: 129 * C57BL/6 * FVB	N	22342750
MGI:5316382	M	MP:0001156	abnormal spermatogenesis	Pum1<tm1.2Hfl>/Pum1<tm1.2Hfl>	involves: 129 * C57BL/6 * FVB	N	22342750
MGI:5316382	M	MP:0001922	reduced male fertility	Pum1<tm1.2Hfl>/Pum1<tm1.2Hfl>	involves: 129 * C57BL/6 * FVB	N	22342750
MGI:5316382	M	MP:0014052	increased male germ cell apoptosis	Pum1<tm1.2Hfl>/Pum1<tm1.2Hfl>	involves: 129 * C57BL/6 * FVB	N	22342750
MGI:5316382	M	MP:0001940	testis hypoplasia	Pum1<tm1.2Hfl>/Pum1<tm1.2Hfl>	involves: 129 * C57BL/6 * FVB	N	22342750
MGI:5316382	M	MP:0001153	small seminiferous tubules	Pum1<tm1.2Hfl>/Pum1<tm1.2Hfl>	involves: 129 * C57BL/6 * FVB	N	22342750
MGI:5316382	M	MP:0004852	decreased testis weight	Pum1<tm1.2Hfl>/Pum1<tm1.2Hfl>	involves: 129 * C57BL/6 * FVB	N	22342750
MGI:5316382	M	MP:0002687	oligozoospermia	Pum1<tm1.2Hfl>/Pum1<tm1.2Hfl>	involves: 129 * C57BL/6 * FVB	N	22342750
MGI:5316383	M	MP:0001153	small seminiferous tubules	Pum1<tm1.2Hfl>/Pum1<tm1.2Hfl>,Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * C57BL/6 * FVB	N	22342750
MGI:5316389	M	MP:0003107	abnormal response to novelty	Fmr1<tm1Cgr>/Y	FVB.129P2-Pde6b<+> Tyr<c-ch> Fmr1<tm1Cgr>/J	N	21364941
MGI:5316389	M	MP:0009141	increased prepulse inhibition	Fmr1<tm1Cgr>/Y	FVB.129P2-Pde6b<+> Tyr<c-ch> Fmr1<tm1Cgr>/J	N	21364941
MGI:5316389	M	MP:0001489	decreased startle reflex	Fmr1<tm1Cgr>/Y	FVB.129P2-Pde6b<+> Tyr<c-ch> Fmr1<tm1Cgr>/J	N	21364941
MGI:5316389	M	MP:0001529	abnormal vocalization	Fmr1<tm1Cgr>/Y	FVB.129P2-Pde6b<+> Tyr<c-ch> Fmr1<tm1Cgr>/J	N	21364941
MGI:5316389	M	MP:0003313	abnormal locomotor activation	Fmr1<tm1Cgr>/Y	FVB.129P2-Pde6b<+> Tyr<c-ch> Fmr1<tm1Cgr>/J	N	21364941
MGI:5316389	M	MP:0001360	abnormal social investigation	Fmr1<tm1Cgr>/Y	FVB.129P2-Pde6b<+> Tyr<c-ch> Fmr1<tm1Cgr>/J	N	21364941
MGI:5316389	M	MP:0001415	increased exploration in new environment	Fmr1<tm1Cgr>/Y	FVB.129P2-Pde6b<+> Tyr<c-ch> Fmr1<tm1Cgr>/J	N	21364941
MGI:5316396	M	MP:0001360	abnormal social investigation	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/Nwu	N	21364941
MGI:5316396	M	MP:0001353	increased aggression towards mice	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/Nwu	N	21364941
MGI:5316396	M	MP:0009141	increased prepulse inhibition	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/Nwu	N	21364941
MGI:5316396	M	MP:0003313	abnormal locomotor activation	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/Nwu	N	21364941
MGI:5316396	M	MP:0001489	decreased startle reflex	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/Nwu	N	21364941
MGI:5316396	M	MP:0003107	abnormal response to novelty	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/Nwu	N	21364941
MGI:5316396	M	MP:0005386	behavior/neurological phenotype	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/Nwu	Y	21364941
MGI:5316396	M	MP:0001441	increased grooming behavior	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>/Nwu	N	21364941
MGI:5316399	M	MP:0001463	abnormal spatial learning	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB/NJ	N	11008180
MGI:5316399	M	MP:0004851	increased testis weight	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB/NJ	N	11008180
MGI:5316399	M	MP:0005391	vision/eye phenotype	Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * FVB/NJ	Y	11008180
MGI:5316427	M	MP:0005188	small penis	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0003402	decreased liver weight	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0005159	azoospermia	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0001925	male infertility	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	F	MP:0005567	decreased circulating total protein level	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0004910	decreased seminal vesicle weight	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	F	MP:0004905	decreased uterus weight	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	F	MP:0004856	decreased ovary weight	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0004929	decreased epididymis weight	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0004930	small epididymis	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	F	MP:0005565	increased blood urea nitrogen level	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0004952	increased spleen weight	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0004955	increased thymus weight	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	F	MP:0001926	female infertility	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0004852	decreased testis weight	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	F	MP:0013308	decreased adrenal gland weight	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0003179	thrombocytopenia	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0002644	decreased circulating triglyceride level	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0004962	decreased prostate gland weight	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0001155	arrest of spermatogenesis	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	F	MP:0001134	absent corpus luteum	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0001157	small seminal vesicle	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	F	MP:0031239	increased atretic ovarian follicle number	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0001147	small testis	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0005559	increased circulating glucose level	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	F	MP:0005179	decreased circulating cholesterol level	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0001262	decreased body weight	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0001154	seminiferous tubule degeneration	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0002774	small prostate gland	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0002968	increased circulating alkaline phosphatase level	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0001145	abnormal male reproductive system morphology	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	F	MP:0001119	abnormal female reproductive system morphology	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0002965	increased circulating serum albumin level	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316427	M	MP:0005536	decreased Leydig cell number	Kiss1r<tm1.1Lex>/Kiss1r<tm1.1Lex>	involves: 129S4/SvJae	N	22067321
MGI:5316428	M	MP:0005016	decreased lymphocyte cell number	Kiss1r<tm1.1Lex>/Kiss1r<+>	involves: 129S4/SvJae	N	22067321
MGI:5316428	M	MP:0005012	decreased eosinophil cell number	Kiss1r<tm1.1Lex>/Kiss1r<+>	involves: 129S4/SvJae	N	22067321
MGI:5316598	F	MP:0005377	hearing/vestibular/ear phenotype	Slc26a5<tm4(cre/ERT2)Jnz>/Slc26a5<+>	involves: 129S6/SvEvTac	Y	21954035
MGI:5316600	F	MP:0005377	hearing/vestibular/ear phenotype	Slc26a5<tm4.1(cre/ERT2)Jnz>/Slc26a5<+>	involves: 129S6/SvEvTac * C57BL/6	Y	21954035
MGI:5316666	F	MP:0011967	increased or absent threshold for auditory brainstem response	Slc26a5<tm4.1(cre/ERT2)Jnz>/Slc26a5<tm4.1(cre/ERT2)Jnz>	involves: 129S6/SvEvTac * C57BL/6	N	21954035
MGI:5316738	F	MP:0001923	reduced female fertility	Astl<tm1Lex>/Astl<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	22206759
MGI:5316873	M	MP:0006380	abnormal spermatid morphology	Piwil1<tm1.1Embrp>/Piwil1<+>	involves: 129S4/SvJaeSor * C57BL/6	N	22121019
MGI:5316873	M	MP:0001925	male infertility	Piwil1<tm1.1Embrp>/Piwil1<+>	involves: 129S4/SvJaeSor * C57BL/6	N	22121019
MGI:5316873	M	MP:0005159	azoospermia	Piwil1<tm1.1Embrp>/Piwil1<+>	involves: 129S4/SvJaeSor * C57BL/6	N	22121019
MGI:5316874	M	MP:0001155	arrest of spermatogenesis	Piwil1<tm1.2Embrp>/Piwil1<tm1.2Embrp>	involves: 129S4/SvJaeSor * BALB/cJ * C57BL/6	N	22121019
MGI:5316874	M	MP:0001925	male infertility	Piwil1<tm1.2Embrp>/Piwil1<tm1.2Embrp>	involves: 129S4/SvJaeSor * BALB/cJ * C57BL/6	N	22121019
MGI:5316874	M	MP:0031620	abnormal chromatoid body morphology	Piwil1<tm1.2Embrp>/Piwil1<tm1.2Embrp>	involves: 129S4/SvJaeSor * BALB/cJ * C57BL/6	N	22121019
MGI:5316875	M	MP:0001925	male infertility	Piwil1<tm1.1Embrp>/Piwil1<tm1.2Embrp>	involves: 129S4/SvJaeSor * BALB/cJ * C57BL/6	N	22121019
MGI:5316875	M	MP:0031620	abnormal chromatoid body morphology	Piwil1<tm1.1Embrp>/Piwil1<tm1.2Embrp>	involves: 129S4/SvJaeSor * BALB/cJ * C57BL/6	N	22121019
MGI:5316875	M	MP:0001155	arrest of spermatogenesis	Piwil1<tm1.1Embrp>/Piwil1<tm1.2Embrp>	involves: 129S4/SvJaeSor * BALB/cJ * C57BL/6	N	22121019
MGI:5317144	M	MP:0011812	increased cranium length	Del(5Gtf2i-Limk1)1Uta/+	involves: 129S7/SvEvBrd * C57BL/6J	N	20049703
MGI:5317145	F	MP:0001139	abnormal vagina morphology	Del(5Limk1-Trim50)2Uta/+	involves: 129S7/SvEvBrd * C57BL/6J	N	20049703
MGI:5317146	F	MP:0001139	abnormal vagina morphology	Del(5Gtf2i-Limk1)1Uta/Del(5Limk1-Trim50)2Uta	involves: 129S7/SvEvBrd * C57BL/6J	N	20049703
MGI:5317456	F	MP:0002169	no abnormal phenotype detected	Hmgn5<tm1.1Mbus>/Hmgn5<tm1.1Mbus>	involves: 129S4/SvJae * C57BL/6J	N	MGI:5427973
MGI:5317961	F	MP:0000704	abnormal thymus development	Il13ra1<tm1Zagh>/Il13ra1<tm1Zagh>	involves: BALB/c * C57BL/6	N	22351937
MGI:5317961	F	MP:0001602	impaired myelopoiesis	Il13ra1<tm1Zagh>/Il13ra1<tm1Zagh>	involves: BALB/c * C57BL/6	N	22351937
MGI:5318047	F	MP:0005367	renal/urinary system phenotype	Wnk3<tm1.1Esoh>/Wnk3<tm1.1Esoh>	involves: 129S4/SvJae * C57BL/6	Y	23213404
MGI:5318047	F	MP:0005376	homeostasis/metabolism phenotype	Wnk3<tm1.1Esoh>/Wnk3<tm1.1Esoh>	involves: 129S4/SvJae * C57BL/6	Y	23213404
MGI:5318047	F	MP:0002843	decreased systemic arterial blood pressure	Wnk3<tm1.1Esoh>/Wnk3<tm1.1Esoh>	involves: 129S4/SvJae * C57BL/6	N	23213404
MGI:5318198	F	MP:0001577	anemia	Xpna/Xpna	involves: 101/H * BALB/c * C3H/HeH	N	MGI:4940633
MGI:5318198	F	MP:0009703	decreased birth body size	Xpna/Xpna	involves: 101/H * BALB/c * C3H/HeH	N	MGI:4940633
MGI:5318199	M	MP:0011091	prenatal lethality, complete penetrance	Xpna/Y	involves: 101/H * BALB/c * C3H/HeH	N	MGI:4940633
MGI:5318247	M	MP:0002075	abnormal coat/hair pigmentation	Atp7a<Mo-5J>/Y	involves: C57BL/6J * DBA/2J	N	MGI:2384330
MGI:5318247	M	MP:0011100	preweaning lethality, complete penetrance	Atp7a<Mo-5J>/Y	involves: C57BL/6J * DBA/2J	N	MGI:2384330
MGI:5318249	F	MP:0010389	mosaic coat color	Atp7a<+>/Atp7a<Mo-5J>	involves: C57BL/6J * DBA/2J	N	MGI:2384330
MGI:5318249	F	MP:0001510	abnormal coat appearance	Atp7a<+>/Atp7a<Mo-5J>	involves: C57BL/6J * DBA/2J	N	MGI:2384330
MGI:5318592	M	MP:0009642	abnormal blood homeostasis	Rhag<tm1Goo>/Rhag<tm1Goo>	involves: 129P2/OlaHsd * C57BL/6	N	19807729
MGI:5319184	M	MP:0002675	asthenozoospermia	Odf1<tm1Shf>/Odf1<tm1Shf>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22037768
MGI:5319184	M	MP:0009831	abnormal sperm midpiece morphology	Odf1<tm1Shf>/Odf1<tm1Shf>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22037768
MGI:5319184	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Odf1<tm1Shf>/Odf1<tm1Shf>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22037768
MGI:5319184	M	MP:0002687	oligozoospermia	Odf1<tm1Shf>/Odf1<tm1Shf>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22037768
MGI:5319184	M	MP:0009238	coiled sperm flagellum	Odf1<tm1Shf>/Odf1<tm1Shf>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22037768
MGI:5319184	M	MP:0001925	male infertility	Odf1<tm1Shf>/Odf1<tm1Shf>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22037768
MGI:5319184	M	MP:0004542	impaired acrosome reaction	Odf1<tm1Shf>/Odf1<tm1Shf>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22037768
MGI:5319184	M	MP:0008893	detached sperm flagellum	Odf1<tm1Shf>/Odf1<tm1Shf>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22037768
MGI:5319185	M	MP:0002675	asthenozoospermia	Odf1<tm1Shf>/Odf1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22037768
MGI:5319214	F	MP:0002208	abnormal germ cell morphology	Cdk16<tm1.2Stge>/Cdk16<tm1.2Stge>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	N	22184064
MGI:5319214	M	MP:0009230	abnormal sperm head morphology	Cdk16<tm1.2Stge>/Cdk16<tm1.2Stge>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	N	22184064
MGI:5319214	M	MP:0001925	male infertility	Cdk16<tm1.2Stge>/Cdk16<tm1.2Stge>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	N	22184064
MGI:5319214	M	MP:0001156	abnormal spermatogenesis	Cdk16<tm1.2Stge>/Cdk16<tm1.2Stge>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	N	22184064
MGI:5319214	M	MP:0002675	asthenozoospermia	Cdk16<tm1.2Stge>/Cdk16<tm1.2Stge>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	N	22184064
MGI:5319214	M	MP:0008892	abnormal sperm flagellum morphology	Cdk16<tm1.2Stge>/Cdk16<tm1.2Stge>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	N	22184064
MGI:5319214	M	MP:0001146	abnormal testis morphology	Cdk16<tm1.2Stge>/Cdk16<tm1.2Stge>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	N	22184064
MGI:5319214	M	MP:0009834	abnormal sperm annulus morphology	Cdk16<tm1.2Stge>/Cdk16<tm1.2Stge>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	N	22184064
MGI:5319214	F	MP:0005389	reproductive system phenotype	Cdk16<tm1.2Stge>/Cdk16<tm1.2Stge>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	Y	22184064
MGI:5319227	F	MP:0009008	delayed estrous cycle	Lepr<tm1.1Chua>/Lepr<tm1.2Chua>,Nos1<tm1(cre)Mgmj>/Nos1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22522563
MGI:5319228	F	MP:0001923	reduced female fertility	Lepr<tm1.2Chua>/Lepr<tm1.2Chua>,Nos1<tm1(cre)Mgmj>/Nos1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22522563
MGI:5319375	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Birc2<tm1.1Rbr>/Birc2<tm1.1Rbr>,Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv * BALB/cJ * C57BL/6	N	22327219
MGI:5319375	F	MP:0001914	hemorrhage	Birc2<tm1.1Rbr>/Birc2<tm1.1Rbr>,Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv * BALB/cJ * C57BL/6	N	22327219
MGI:5319375	F	MP:0000291	enlarged pericardium	Birc2<tm1.1Rbr>/Birc2<tm1.1Rbr>,Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv * BALB/cJ * C57BL/6	N	22327219
MGI:5319375	F	MP:0005140	decreased cardiac muscle contractility	Birc2<tm1.1Rbr>/Birc2<tm1.1Rbr>,Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv * BALB/cJ * C57BL/6	N	22327219
MGI:5319375	F	MP:0006138	congestive heart failure	Birc2<tm1.1Rbr>/Birc2<tm1.1Rbr>,Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv * BALB/cJ * C57BL/6	N	22327219
MGI:5319375	F	MP:0005244	hemopericardium	Birc2<tm1.1Rbr>/Birc2<tm1.1Rbr>,Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv * BALB/cJ * C57BL/6	N	22327219
MGI:5319375	F	MP:0003105	abnormal heart atrium morphology	Birc2<tm1.1Rbr>/Birc2<tm1.1Rbr>,Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv * BALB/cJ * C57BL/6	N	22327219
MGI:5319376	F	MP:0005244	hemopericardium	Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv	N	22327219
MGI:5319376	F	MP:0000291	enlarged pericardium	Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv	N	22327219
MGI:5319376	F	MP:0001914	hemorrhage	Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv	N	22327219
MGI:5319376	F	MP:0006138	congestive heart failure	Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv	N	22327219
MGI:5319376	F	MP:0005140	decreased cardiac muscle contractility	Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv	N	22327219
MGI:5319376	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv	N	22327219
MGI:5319376	F	MP:0003105	abnormal heart atrium morphology	Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv	N	22327219
MGI:5319377	F	MP:0002169	no abnormal phenotype detected	Birc3<tm1.1Rbr>/Birc3<tm1.1Rbr>,Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv * C57BL/6 * SJL	N	22327219
MGI:5319382	F	MP:0011099	lethality throughout fetal growth and development, complete penetrance	Birc2<tm1.1Rbr>/Birc2<tm1.1Rbr>,Ripk1<tm1Led>/Ripk1<tm1Led>,Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv * 129S6/SvEvTac * BALB/cJ * C57BL/6	N	22327219
MGI:5319383	F	MP:0011086	postnatal lethality, incomplete penetrance	Birc2<tm1.1Rbr>/Birc2<tm1.1Rbr>,Ripk1<tm1Led>/Ripk1<+>,Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv * 129S6/SvEvTac * BALB/cJ * C57BL/6	N	22327219
MGI:5319383	F	MP:0001265	decreased body size	Birc2<tm1.1Rbr>/Birc2<tm1.1Rbr>,Ripk1<tm1Led>/Ripk1<+>,Xiap<tm1Vdr>/Xiap<tm1Vdr>	involves: 129S1/Sv * 129S6/SvEvTac * BALB/cJ * C57BL/6	N	22327219
MGI:5319484	F	MP:0008211	decreased mature B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<tm1.1Ldn>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319484	F	MP:0002827	abnormal renal corpuscle morphology	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<tm1.1Ldn>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319484	F	MP:0005017	decreased B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<tm1.1Ldn>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319484	F	MP:0008177	increased germinal center B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<tm1.1Ldn>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319484	F	MP:0008097	increased plasma cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<tm1.1Ldn>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319484	F	MP:0008182	decreased marginal zone B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<tm1.1Ldn>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319484	F	MP:0008174	decreased follicular B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<tm1.1Ldn>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319484	F	MP:0003725	increased autoantibody level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<tm1.1Ldn>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319484	F	MP:0002459	abnormal B cell physiology	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<tm1.1Ldn>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319484	F	MP:0004771	increased anti-single stranded DNA antibody level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<tm1.1Ldn>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319484	F	MP:0002494	increased IgM level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<tm1.1Ldn>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319484	F	MP:0004829	increased anti-chromatin antibody level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<tm1.1Ldn>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319484	F	MP:0004762	increased anti-double stranded DNA antibody level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<tm1.1Ldn>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319485	M	MP:0004829	increased anti-chromatin antibody level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Y	involves: BALB/c * C57BL/6	N	22302739
MGI:5319485	M	MP:0008177	increased germinal center B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Y	involves: BALB/c * C57BL/6	N	22302739
MGI:5319485	M	MP:0005017	decreased B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Y	involves: BALB/c * C57BL/6	N	22302739
MGI:5319485	M	MP:0004762	increased anti-double stranded DNA antibody level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Y	involves: BALB/c * C57BL/6	N	22302739
MGI:5319485	M	MP:0004771	increased anti-single stranded DNA antibody level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Y	involves: BALB/c * C57BL/6	N	22302739
MGI:5319485	M	MP:0008211	decreased mature B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Y	involves: BALB/c * C57BL/6	N	22302739
MGI:5319485	M	MP:0002494	increased IgM level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Y	involves: BALB/c * C57BL/6	N	22302739
MGI:5319485	M	MP:0008097	increased plasma cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Y	involves: BALB/c * C57BL/6	N	22302739
MGI:5319485	M	MP:0003725	increased autoantibody level	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Y	involves: BALB/c * C57BL/6	N	22302739
MGI:5319485	M	MP:0008182	decreased marginal zone B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Y	involves: BALB/c * C57BL/6	N	22302739
MGI:5319485	M	MP:0002827	abnormal renal corpuscle morphology	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Y	involves: BALB/c * C57BL/6	N	22302739
MGI:5319485	M	MP:0002459	abnormal B cell physiology	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Y	involves: BALB/c * C57BL/6	N	22302739
MGI:5319485	M	MP:0008174	decreased follicular B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Y	involves: BALB/c * C57BL/6	N	22302739
MGI:5319486	F	MP:0005153	abnormal B cell proliferation	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<+>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319486	F	MP:0002458	abnormal B cell number	Cd79a<tm1(cre)Reth>/Cd79a<+>,Was<tm1.1Ldn>/Was<+>	involves: BALB/c * C57BL/6	N	22302739
MGI:5319488	F	MP:0003725	increased autoantibody level	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0008182	decreased marginal zone B cell number	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0002459	abnormal B cell physiology	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0004829	increased anti-chromatin antibody level	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0008211	decreased mature B cell number	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0004762	increased anti-double stranded DNA antibody level	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0008097	increased plasma cell number	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0008177	increased germinal center B cell number	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0002495	increased IgA level	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0004771	increased anti-single stranded DNA antibody level	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0002497	increased IgE level	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0003179	thrombocytopenia	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0002494	increased IgM level	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0002827	abnormal renal corpuscle morphology	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319488	F	MP:0002417	abnormal megakaryocyte morphology	Was<tm1Sbs>/Was<tm1Sbs>	involves: 129S6/SvEvTac * C57BL/6	N	23305739
MGI:5319489	M	MP:0003179	thrombocytopenia	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319489	M	MP:0002497	increased IgE level	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319489	M	MP:0008177	increased germinal center B cell number	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319489	M	MP:0004762	increased anti-double stranded DNA antibody level	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319489	M	MP:0002495	increased IgA level	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319489	M	MP:0008211	decreased mature B cell number	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319489	M	MP:0002459	abnormal B cell physiology	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319489	M	MP:0002494	increased IgM level	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319489	M	MP:0002827	abnormal renal corpuscle morphology	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319489	M	MP:0008182	decreased marginal zone B cell number	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319489	M	MP:0004771	increased anti-single stranded DNA antibody level	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319489	M	MP:0003725	increased autoantibody level	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319489	M	MP:0008097	increased plasma cell number	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319489	M	MP:0004829	increased anti-chromatin antibody level	Was<tm1Sbs>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22302739
MGI:5319635	F	MP:0001926	female infertility	Lep<ob>/Lep<ob>,Pmch<tm1.1(HBEGF)Rpa>/Pmch<+>	B6.Cg-Lep<ob> Pmch<tm1.1(DTR)Rpa>	N	22232663
MGI:5319635	M	MP:0001922	reduced male fertility	Lep<ob>/Lep<ob>,Pmch<tm1.1(HBEGF)Rpa>/Pmch<+>	B6.Cg-Lep<ob> Pmch<tm1.1(DTR)Rpa>	N	22232663
MGI:5319676	M	MP:0001922	reduced male fertility	Cdk2<tm1.1Jro>/Cdk2<+>	involves: 129S1/SvlmJ * 129S4/SvJaeSor * C57BL/6	N	22331465
MGI:5319676	M	MP:0003205	testicular atrophy	Cdk2<tm1.1Jro>/Cdk2<+>	involves: 129S1/SvlmJ * 129S4/SvJaeSor * C57BL/6	N	22331465
MGI:5319676	M	MP:0005159	azoospermia	Cdk2<tm1.1Jro>/Cdk2<+>	involves: 129S1/SvlmJ * 129S4/SvJaeSor * C57BL/6	N	22331465
MGI:5319784	F	MP:0001385	pup cannibalization	Inhbb<tm1Grid>/Inhbb<tm1Grid>	involves: 129S1/Sv * C57BL/6	N	7947320
MGI:5319784	F	MP:0001386	abnormal maternal nurturing	Inhbb<tm1Grid>/Inhbb<tm1Grid>	involves: 129S1/Sv * C57BL/6	N	7947320
MGI:5320585	F	MP:0004753	abnormal miniature excitatory postsynaptic currents	Nlgn3<tm3.1Sud>/Nlgn3<tm3.1Sud>	involves: 129S1/Sv * 129X1/SvJ	N	21642956
MGI:5320585	F	MP:0011003	reduced AMPA-mediated synaptic currents	Nlgn3<tm3.1Sud>/Nlgn3<tm3.1Sud>	involves: 129S1/Sv * 129X1/SvJ	N	21642956
MGI:5320585	F	MP:0002912	abnormal excitatory postsynaptic potential	Nlgn3<tm3.1Sud>/Nlgn3<tm3.1Sud>	involves: 129S1/Sv * 129X1/SvJ	N	21642956
MGI:5320585	F	MP:0002886	abnormal glutamate-mediated receptor currents	Nlgn3<tm3.1Sud>/Nlgn3<tm3.1Sud>	involves: 129S1/Sv * 129X1/SvJ	N	21642956
MGI:5320585	F	MP:0003631	nervous system phenotype	Nlgn3<tm3.1Sud>/Nlgn3<tm3.1Sud>	involves: 129S1/Sv * 129X1/SvJ	Y	21642956
MGI:5320624	M	MP:0001925	male infertility	Vm/Vm<+>	involves: 101/H * C3H/HeH	N	MGI:3044155
MGI:5320624	M	MP:0001922	reduced male fertility	Vm/Vm<+>	involves: 101/H * C3H/HeH	N	MGI:3044155
MGI:5320672	M	MP:0008280	abnormal male germ cell apoptosis	Piwil2<tm1.1Doca>/Piwil2<tm1.1Doca>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	22020280
MGI:5320672	M	MP:0001925	male infertility	Piwil2<tm1.1Doca>/Piwil2<tm1.1Doca>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	22020280
MGI:5320672	M	MP:0008261	arrest of male meiosis	Piwil2<tm1.1Doca>/Piwil2<tm1.1Doca>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	22020280
MGI:5320672	M	MP:0003205	testicular atrophy	Piwil2<tm1.1Doca>/Piwil2<tm1.1Doca>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	22020280
MGI:5320674	M	MP:0004852	decreased testis weight	Piwil4<tm2.1Doca>/Piwil4<tm2.1Doca>	involves: 129P2/OlaHsd * BALB/cJ	N	22020280
MGI:5425369	M	MP:0020869	immotile sperm	Mns1<tm1Jw>/Mns1<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	22396656
MGI:5425369	M	MP:0009237	kinked sperm flagellum	Mns1<tm1Jw>/Mns1<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	22396656
MGI:5425369	M	MP:0006380	abnormal spermatid morphology	Mns1<tm1Jw>/Mns1<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	22396656
MGI:5425369	M	MP:0009239	short sperm flagellum	Mns1<tm1Jw>/Mns1<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	22396656
MGI:5425369	M	MP:0009838	abnormal sperm axoneme morphology	Mns1<tm1Jw>/Mns1<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	22396656
MGI:5425369	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Mns1<tm1Jw>/Mns1<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	22396656
MGI:5425369	M	MP:0030591	absent sperm fibrous sheath	Mns1<tm1Jw>/Mns1<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	22396656
MGI:5425369	M	MP:0031356	abnormal outer dense fiber morphology	Mns1<tm1Jw>/Mns1<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	22396656
MGI:5425369	M	MP:0002687	oligozoospermia	Mns1<tm1Jw>/Mns1<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	22396656
MGI:5425369	M	MP:0002631	abnormal epididymis morphology	Mns1<tm1Jw>/Mns1<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	22396656
MGI:5425369	M	MP:0004852	decreased testis weight	Mns1<tm1Jw>/Mns1<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	22396656
MGI:5425369	M	MP:0008892	abnormal sperm flagellum morphology	Mns1<tm1Jw>/Mns1<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	22396656
MGI:5425369	M	MP:0001925	male infertility	Mns1<tm1Jw>/Mns1<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	22396656
MGI:5425546	F	MP:0001394	circling	Phex<Mhdabap012>/Phex<Mhdabap012>	C3HeB/FeJ-Phex<Mhdabap012>	N	22527485
MGI:5425546	F	MP:0014322	short hindlimb	Phex<Mhdabap012>/Phex<Mhdabap012>	C3HeB/FeJ-Phex<Mhdabap012>	N	22527485
MGI:5425546	F	MP:0002968	increased circulating alkaline phosphatase level	Phex<Mhdabap012>/Phex<Mhdabap012>	C3HeB/FeJ-Phex<Mhdabap012>	N	22527485
MGI:5425546	F	MP:0000198	decreased circulating phosphate level	Phex<Mhdabap012>/Phex<Mhdabap012>	C3HeB/FeJ-Phex<Mhdabap012>	N	22527485
MGI:5425550	M	MP:0004353	abnormal deltoid tuberosity morphology	Tent5a<m1Mhda>/Tent5a<m1Mhda>	C3HeB/FeJ-Tent5a<m1Mhda>	N	26803617
MGI:5425550	M	MP:0002932	abnormal joint morphology	Tent5a<m1Mhda>/Tent5a<m1Mhda>	C3HeB/FeJ-Tent5a<m1Mhda>	N	26803617
MGI:5425550	M	MP:0009728	abnormal calcaneum morphology	Tent5a<m1Mhda>/Tent5a<m1Mhda>	C3HeB/FeJ-Tent5a<m1Mhda>	N	26803617
MGI:5425550	M	MP:0000558	abnormal tibia morphology	Tent5a<m1Mhda>/Tent5a<m1Mhda>	C3HeB/FeJ-Tent5a<m1Mhda>	N	26803617
MGI:5425550	M	MP:0004703	abnormal vertebral column morphology	Tent5a<m1Mhda>/Tent5a<m1Mhda>	C3HeB/FeJ-Tent5a<m1Mhda>	N	26803617
MGI:5425550	M	MP:0008158	increased diameter of femur	Tent5a<m1Mhda>/Tent5a<m1Mhda>	C3HeB/FeJ-Tent5a<m1Mhda>	N	26803617
MGI:5425550	M	MP:0005508	abnormal skeleton morphology	Tent5a<m1Mhda>/Tent5a<m1Mhda>	C3HeB/FeJ-Tent5a<m1Mhda>	N	26803617
MGI:5425687	F	MP:0000198	decreased circulating phosphate level	Phex<Mhdabap024>/Phex<Mhdabap024>	C3HeB/FeJ-Phex<Mhdabap024>	N	22527485
MGI:5425687	F	MP:0002966	decreased circulating alkaline phosphatase level	Phex<Mhdabap024>/Phex<Mhdabap024>	C3HeB/FeJ-Phex<Mhdabap024>	N	22527485
MGI:5425687	F	MP:0001265	decreased body size	Phex<Mhdabap024>/Phex<Mhdabap024>	C3HeB/FeJ-Phex<Mhdabap024>	N	22527485
MGI:5425687	F	MP:0001394	circling	Phex<Mhdabap024>/Phex<Mhdabap024>	C3HeB/FeJ-Phex<Mhdabap024>	N	22527485
MGI:5426387	F	MP:0001923	reduced female fertility	Airn<tm2.1Dpb>/Airn<tm2.1Dpb>	involves: 129S2/SvPas * 129S4/SvJaeSor * FVB/N	N	22396659
MGI:5426419	M	MP:0005385	cardiovascular system phenotype	Rgs2<tm1.1Kjb>/Rgs2<tm1.1Kjb>,X/Tg(Myh11-icre/ERT2)1Soff	involves: 129X1/SvJ * C57BL/6 * FVB/N	Y	22354966
MGI:5426705	F	MP:0001923	reduced female fertility	Nr1d1<tm1.2Rev>/Nr1d1<tm1.2Rev>	involves: BALB/cJ * C57BL/6J	N	22460952
MGI:5426705	M	MP:0001922	reduced male fertility	Nr1d1<tm1.2Rev>/Nr1d1<tm1.2Rev>	involves: BALB/cJ * C57BL/6J	N	22460952
MGI:5426790	M	MP:0001402	decreased locomotor activity	Maged1<tm1Tnab>/Y	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426790	M	MP:0009710	anhedonia	Maged1<tm1Tnab>/Y	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426790	M	MP:0010070	decreased serotonin level	Maged1<tm1Tnab>/Y	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426790	M	MP:0001361	social withdrawal	Maged1<tm1Tnab>/Y	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426790	M	MP:0005386	behavior/neurological phenotype	Maged1<tm1Tnab>/Y	B6.129P2-Maged1<tm1Tnab>	Y	22457503
MGI:5426790	M	MP:0002573	behavioral despair	Maged1<tm1Tnab>/Y	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426790	M	MP:0001417	decreased exploration in new environment	Maged1<tm1Tnab>/Y	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426790	M	MP:0010069	increased serotonin level	Maged1<tm1Tnab>/Y	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426790	M	MP:0005322	abnormal serotonin level	Maged1<tm1Tnab>/Y	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426791	F	MP:0009710	anhedonia	Maged1<tm1Tnab>/Maged1<tm1Tnab>	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426791	F	MP:0010069	increased serotonin level	Maged1<tm1Tnab>/Maged1<tm1Tnab>	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426791	F	MP:0010070	decreased serotonin level	Maged1<tm1Tnab>/Maged1<tm1Tnab>	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426791	F	MP:0001417	decreased exploration in new environment	Maged1<tm1Tnab>/Maged1<tm1Tnab>	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426791	F	MP:0001402	decreased locomotor activity	Maged1<tm1Tnab>/Maged1<tm1Tnab>	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426791	F	MP:0005386	behavior/neurological phenotype	Maged1<tm1Tnab>/Maged1<tm1Tnab>	B6.129P2-Maged1<tm1Tnab>	Y	22457503
MGI:5426791	F	MP:0005322	abnormal serotonin level	Maged1<tm1Tnab>/Maged1<tm1Tnab>	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426791	F	MP:0002573	behavioral despair	Maged1<tm1Tnab>/Maged1<tm1Tnab>	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426791	F	MP:0001361	social withdrawal	Maged1<tm1Tnab>/Maged1<tm1Tnab>	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426793	F	MP:0001361	social withdrawal	Maged1<tm1Tnab>/Maged1<+>	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426793	F	MP:0001402	decreased locomotor activity	Maged1<tm1Tnab>/Maged1<+>	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426793	F	MP:0002573	behavioral despair	Maged1<tm1Tnab>/Maged1<+>	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5426793	F	MP:0001417	decreased exploration in new environment	Maged1<tm1Tnab>/Maged1<+>	B6.129P2-Maged1<tm1Tnab>	N	22457503
MGI:5427006	F	MP:0001386	abnormal maternal nurturing	Nags<tm1(KOMP)Vlcg>/Nags<+>	C57BL/6N-Nags<tm1(KOMP)Vlcg>	N	22503289
MGI:5427349	M	MP:0002169	no abnormal phenotype detected	Smarca1<tm1Pick>/Y,Tg(Gata1-cre)1Sho/0	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427350	F	MP:0009937	abnormal neuron differentiation	Smarca1<tm1.1Pick>/Smarca1<tm1.1Pick>	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427350	F	MP:0000788	abnormal cerebral cortex morphology	Smarca1<tm1.1Pick>/Smarca1<tm1.1Pick>	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427350	F	MP:0004948	abnormal neuronal precursor proliferation	Smarca1<tm1.1Pick>/Smarca1<tm1.1Pick>	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427350	F	MP:0000934	abnormal telencephalon development	Smarca1<tm1.1Pick>/Smarca1<tm1.1Pick>	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427350	F	MP:0002176	increased brain weight	Smarca1<tm1.1Pick>/Smarca1<tm1.1Pick>	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427350	F	MP:0008458	abnormal cortical ventricular zone morphology	Smarca1<tm1.1Pick>/Smarca1<tm1.1Pick>	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427350	F	MP:0004046	abnormal mitosis	Smarca1<tm1.1Pick>/Smarca1<tm1.1Pick>	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427350	F	MP:0002833	increased heart weight	Smarca1<tm1.1Pick>/Smarca1<tm1.1Pick>	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427350	F	MP:0000789	thickened cerebral cortex	Smarca1<tm1.1Pick>/Smarca1<tm1.1Pick>	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427351	M	MP:0005386	behavior/neurological phenotype	Smarca1<tm1.1Pick>/Y	involves: 129S4/SvJae * CD-1	Y	22516202
MGI:5427351	M	MP:0000934	abnormal telencephalon development	Smarca1<tm1.1Pick>/Y	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427351	M	MP:0009937	abnormal neuron differentiation	Smarca1<tm1.1Pick>/Y	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427351	M	MP:0000788	abnormal cerebral cortex morphology	Smarca1<tm1.1Pick>/Y	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427351	M	MP:0008458	abnormal cortical ventricular zone morphology	Smarca1<tm1.1Pick>/Y	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427351	M	MP:0002176	increased brain weight	Smarca1<tm1.1Pick>/Y	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427351	M	MP:0000434	megacephaly	Smarca1<tm1.1Pick>/Y	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427351	M	MP:0000789	thickened cerebral cortex	Smarca1<tm1.1Pick>/Y	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427351	M	MP:0002833	increased heart weight	Smarca1<tm1.1Pick>/Y	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427351	M	MP:0004948	abnormal neuronal precursor proliferation	Smarca1<tm1.1Pick>/Y	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427351	M	MP:0004046	abnormal mitosis	Smarca1<tm1.1Pick>/Y	involves: 129S4/SvJae * CD-1	N	22516202
MGI:5427352	M	MP:0003631	nervous system phenotype	Smarca1<tm1.1Pick>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: 129P2/OlaHsd * 129S4/SvJae * CD-1	Y	22516202
MGI:5427453	M	MP:0003631	nervous system phenotype	Hprt1<tm86(NR2E1,bEMS223)Ems>/Y	B6.Cg-Hprt1<tm86(NR2E1,bEMS223)Ems>	Y	22290436
MGI:5427453	M	MP:0004948	abnormal neuronal precursor proliferation	Hprt1<tm86(NR2E1,bEMS223)Ems>/Y	B6.Cg-Hprt1<tm86(NR2E1,bEMS223)Ems>	N	22290436
MGI:5427453	M	MP:0005391	vision/eye phenotype	Hprt1<tm86(NR2E1,bEMS223)Ems>/Y	B6.Cg-Hprt1<tm86(NR2E1,bEMS223)Ems>	Y	22290436
MGI:5427453	M	MP:0005385	cardiovascular system phenotype	Hprt1<tm86(NR2E1,bEMS223)Ems>/Y	B6.Cg-Hprt1<tm86(NR2E1,bEMS223)Ems>	Y	22290436
MGI:5427454	M	MP:0002741	small olfactory bulb	Hprt1<tm86(NR2E1,bEMS223)Ems>/Y,Nr2e1<frc>/Nr2e1<frc>	involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6	N	22290436
MGI:5427454	M	MP:0005391	vision/eye phenotype	Hprt1<tm86(NR2E1,bEMS223)Ems>/Y,Nr2e1<frc>/Nr2e1<frc>	involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6	Y	22290436
MGI:5427454	M	MP:0008540	abnormal cerebral hemisphere morphology	Hprt1<tm86(NR2E1,bEMS223)Ems>/Y,Nr2e1<frc>/Nr2e1<frc>	involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6	N	22290436
MGI:5427454	M	MP:0004948	abnormal neuronal precursor proliferation	Hprt1<tm86(NR2E1,bEMS223)Ems>/Y,Nr2e1<frc>/Nr2e1<frc>	involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6	N	22290436
MGI:5427454	M	MP:0005385	cardiovascular system phenotype	Hprt1<tm86(NR2E1,bEMS223)Ems>/Y,Nr2e1<frc>/Nr2e1<frc>	involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6	Y	22290436
MGI:5427497	M	MP:0000659	prostate gland hyperplasia	Gt(ROSA)26Sor<tm1(CAG-Bmi1,-EGFP)Nki>/Gt(ROSA)26Sor<+>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * FVB/N	N	22505453
MGI:5427497	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Gt(ROSA)26Sor<tm1(CAG-Bmi1,-EGFP)Nki>/Gt(ROSA)26Sor<+>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * FVB/N	N	22505453
MGI:5427498	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Gt(ROSA)26Sor<tm1(CAG-Bmi1,-EGFP)Nki>/Gt(ROSA)26Sor<+>,Pten<tm1Mro>/Pten<+>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * FVB/N	N	22505453
MGI:5427498	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Gt(ROSA)26Sor<tm1(CAG-Bmi1,-EGFP)Nki>/Gt(ROSA)26Sor<+>,Pten<tm1Mro>/Pten<+>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * FVB/N	N	22505453
MGI:5427499	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Mro>/Pten<+>,Tg(Pbsn-cre)4Prb/0	involves: C57BL/6 * DBA/2	N	22505453
MGI:5427500	M	MP:0001544	abnormal cardiovascular system physiology	Cfp<tm1Cmst>/Y	involves: 129P2/OlaHsd * C57BL/6	N	22308431
MGI:5427500	M	MP:0005166	decreased susceptibility to injury	Cfp<tm1Cmst>/Y	involves: 129P2/OlaHsd * C57BL/6	N	22308431
MGI:5427584	F	MP:0001126	abnormal ovary morphology	Pik3ca<tm1.1Waph>/Pik3ca<+>	involves: 129S1/Sv * C57BL/6	N	22214849
MGI:5427585	F	MP:0012411	increased granulosa cell tumor incidence	Pik3ca<tm1.1Waph>/Pik3ca<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * BALB/c * C57BL/6	N	22214849
MGI:5427585	F	MP:0001126	abnormal ovary morphology	Pik3ca<tm1.1Waph>/Pik3ca<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * BALB/c * C57BL/6	N	22214849
MGI:5427585	F	MP:0003507	abnormal ovary physiology	Pik3ca<tm1.1Waph>/Pik3ca<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * BALB/c * C57BL/6	N	22214849
MGI:5427585	F	MP:0004834	ovary hemorrhage	Pik3ca<tm1.1Waph>/Pik3ca<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * BALB/c * C57BL/6	N	22214849
MGI:5427585	F	MP:0008000	increased ovary tumor incidence	Pik3ca<tm1.1Waph>/Pik3ca<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * BALB/c * C57BL/6	N	22214849
MGI:5427611	M	MP:0001925	male infertility	Hormad2<tm1Atot>/Hormad2<tm1Atot>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	22549958
MGI:5427611	M	MP:0008280	abnormal male germ cell apoptosis	Hormad2<tm1Atot>/Hormad2<tm1Atot>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	22549958
MGI:5427611	M	MP:0005169	abnormal male meiosis	Hormad2<tm1Atot>/Hormad2<tm1Atot>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	22549958
MGI:5427611	M	MP:0001155	arrest of spermatogenesis	Hormad2<tm1Atot>/Hormad2<tm1Atot>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd	N	22549958
MGI:5427612	M	MP:0001155	arrest of spermatogenesis	Hormad2<tm1.2Atot>/Hormad2<tm1.2Atot>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * SJL	N	22549958
MGI:5427612	M	MP:0001925	male infertility	Hormad2<tm1.2Atot>/Hormad2<tm1.2Atot>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * SJL	N	22549958
MGI:5427612	M	MP:0005169	abnormal male meiosis	Hormad2<tm1.2Atot>/Hormad2<tm1.2Atot>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * SJL	N	22549958
MGI:5427612	F	MP:0005168	abnormal female meiosis	Hormad2<tm1.2Atot>/Hormad2<tm1.2Atot>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * SJL	N	22549958
MGI:5427612	M	MP:0008280	abnormal male germ cell apoptosis	Hormad2<tm1.2Atot>/Hormad2<tm1.2Atot>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * SJL	N	22549958
MGI:5427613	F	MP:0005431	decreased oocyte number	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ	N	23039116
MGI:5427613	F	MP:0001127	small ovary	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ	N	23039116
MGI:5427613	F	MP:0005168	abnormal female meiosis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ	N	23039116
MGI:5427613	F	MP:0004856	decreased ovary weight	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ	N	23039116
MGI:5427613	F	MP:0005431	decreased oocyte number	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ	N	22549958
MGI:5427616	F	MP:0004805	absent oocytes	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>,Hormad2<tm1.2Atot>/Hormad2<tm1.2Atot>	involves: 129 * BALB/c * C57BL/6 * SJL	N	22549958
MGI:5427619	F	MP:0001376	abnormal mating receptivity	Fuom<tm1Ckp>/Fuom<tm1Ckp>	involves: 129P2/OlaHsd * C57BL/6	N	20609214
MGI:5427619	F	MP:0002566	abnormal sexual interaction	Fuom<tm1Ckp>/Fuom<tm1Ckp>	involves: 129P2/OlaHsd * C57BL/6	N	20609214
MGI:5427620	F	MP:0001376	abnormal mating receptivity	Fuom<tm1Ckp>/Fuom<+>	involves: 129P2/OlaHsd * C57BL/6	N	20609214
MGI:5427622	M	MP:0011110	preweaning lethality, incomplete penetrance	Mecp2<tm1.1Mitoh>/Y	Not Specified	N	22375006
MGI:5427622	M	MP:0003631	nervous system phenotype	Mecp2<tm1.1Mitoh>/Y	Not Specified	Y	22375006
MGI:5427622	M	MP:0009658	increased placenta apoptosis	Mecp2<tm1.1Mitoh>/Y	Not Specified	N	22375006
MGI:5427622	M	MP:0001711	abnormal placenta morphology	Mecp2<tm1.1Mitoh>/Y	Not Specified	N	22375006
MGI:5427623	F	MP:0001711	abnormal placenta morphology	Mecp2<tm1.1Mitoh>/Mecp2<+>	Not Specified	N	22375006
MGI:5427623	F	MP:0003631	nervous system phenotype	Mecp2<tm1.1Mitoh>/Mecp2<+>	Not Specified	Y	22375006
MGI:5427623	F	MP:0011110	preweaning lethality, incomplete penetrance	Mecp2<tm1.1Mitoh>/Mecp2<+>	Not Specified	N	22375006
MGI:5427623	F	MP:0009658	increased placenta apoptosis	Mecp2<tm1.1Mitoh>/Mecp2<+>	Not Specified	N	22375006
MGI:5427624	F	MP:0011110	preweaning lethality, incomplete penetrance	Mecp2<tm1.1Mitoh>/Mecp2<tm1.1Mitoh>	Not Specified	N	22375006
MGI:5427846	F	MP:0000628	abnormal mammary gland development	Zfp157<Gt(XC356)Byg>/Zfp157<Gt(XC356)Byg>	involves: 129P2/OlaHsd	N	22588720
MGI:5427846	F	MP:0001884	mammary gland alveolar hyperplasia	Zfp157<Gt(XC356)Byg>/Zfp157<Gt(XC356)Byg>	involves: 129P2/OlaHsd	N	22588720
MGI:5427846	F	MP:0001881	abnormal mammary gland physiology	Zfp157<Gt(XC356)Byg>/Zfp157<Gt(XC356)Byg>	involves: 129P2/OlaHsd	N	22588720
MGI:5427846	F	MP:0006269	abnormal mammary gland growth during pregnancy	Zfp157<Gt(XC356)Byg>/Zfp157<Gt(XC356)Byg>	involves: 129P2/OlaHsd	N	22588720
MGI:5427846	F	MP:0000627	abnormal mammary gland morphology	Zfp157<Gt(XC356)Byg>/Zfp157<Gt(XC356)Byg>	involves: 129P2/OlaHsd	N	22588720
MGI:5427847	F	MP:0013781	abnormal mammary gland luminal epithelium morphology	Gata3<tm1Jfz>/Gata3<tm1Jfz>,Zfp157<Gt(XC356)Byg>/Zfp157<Gt(XC356)Byg>,Tg(LGB-cre)74Acl/0	involves: 129 * C57BL/6 * CBA	N	22588720
MGI:5427849	F	MP:0010249	lactation failure	Gata3<tm1Jfz>/Gata3<tm1Jfz>,Tg(LGB-cre)74Acl/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	22588720
MGI:5427849	F	MP:0006270	abnormal mammary gland growth during lactation	Gata3<tm1Jfz>/Gata3<tm1Jfz>,Tg(LGB-cre)74Acl/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	22588720
MGI:5427882	F	MP:0001923	reduced female fertility	Astl<tm1Dean>/Astl<tm1Dean>	involves: 129S6/SvEvTac	N	22472438
MGI:5427911	M	MP:0002169	no abnormal phenotype detected	Egfl6<tm1Ksek>/Y	involves: 129 * C57BL/6	N	22613833
MGI:5427950	M	MP:0000691	enlarged spleen	Fcgr2b<tm1.2Jsv>/Fcgr2b<+>,X/Yaa	involves: C57BL/6 * FVB/N * SB/Le	N	21724994
MGI:5427950	M	MP:0004801	increased susceptibility to systemic lupus erythematosus	Fcgr2b<tm1.2Jsv>/Fcgr2b<+>,X/Yaa	involves: C57BL/6 * FVB/N * SB/Le	N	21724994
MGI:5427950	M	MP:0002083	premature death	Fcgr2b<tm1.2Jsv>/Fcgr2b<+>,X/Yaa	involves: C57BL/6 * FVB/N * SB/Le	N	21724994
MGI:5427950	M	MP:0000220	increased monocyte cell number	Fcgr2b<tm1.2Jsv>/Fcgr2b<+>,X/Yaa	involves: C57BL/6 * FVB/N * SB/Le	N	21724994
MGI:5427950	M	MP:0004762	increased anti-double stranded DNA antibody level	Fcgr2b<tm1.2Jsv>/Fcgr2b<+>,X/Yaa	involves: C57BL/6 * FVB/N * SB/Le	N	21724994
MGI:5427950	M	MP:0004829	increased anti-chromatin antibody level	Fcgr2b<tm1.2Jsv>/Fcgr2b<+>,X/Yaa	involves: C57BL/6 * FVB/N * SB/Le	N	21724994
MGI:5427950	M	MP:0002135	abnormal kidney morphology	Fcgr2b<tm1.2Jsv>/Fcgr2b<+>,X/Yaa	involves: C57BL/6 * FVB/N * SB/Le	N	21724994
MGI:5427958	M	MP:0002089	abnormal postnatal growth/weight/body size	Acsl3<Gt(OST148301)Lex>/Acsl3<Gt(OST148301)Lex>	B6;129S5-Acsl3<Gt(OST148301)Lex>/Orl	N	MGI:2655403
MGI:5427958	M	MP:0003961	decreased lean body mass	Acsl3<Gt(OST148301)Lex>/Acsl3<Gt(OST148301)Lex>	B6;129S5-Acsl3<Gt(OST148301)Lex>/Orl	N	MGI:2655403
MGI:5427958	M	MP:0001732	postnatal growth retardation	Acsl3<Gt(OST148301)Lex>/Acsl3<Gt(OST148301)Lex>	B6;129S5-Acsl3<Gt(OST148301)Lex>/Orl	N	MGI:2655403
MGI:5427958	M	MP:0001258	decreased body length	Acsl3<Gt(OST148301)Lex>/Acsl3<Gt(OST148301)Lex>	B6;129S5-Acsl3<Gt(OST148301)Lex>/Orl	N	MGI:2655403
MGI:5427958	M	MP:0001262	decreased body weight	Acsl3<Gt(OST148301)Lex>/Acsl3<Gt(OST148301)Lex>	B6;129S5-Acsl3<Gt(OST148301)Lex>/Orl	N	MGI:2655403
MGI:5427980	M	MP:0002784	abnormal Sertoli cell morphology	Katnal1<1H>/Katnal1<1H>	involves: C3H/HeH * C57BL/6J	N	22654668
MGI:5427980	M	MP:0002687	oligozoospermia	Katnal1<1H>/Katnal1<1H>	involves: C3H/HeH * C57BL/6J	N	22654668
MGI:5427980	M	MP:0001925	male infertility	Katnal1<1H>/Katnal1<1H>	involves: C3H/HeH * C57BL/6J	N	22654668
MGI:5427980	M	MP:0001153	small seminiferous tubules	Katnal1<1H>/Katnal1<1H>	involves: C3H/HeH * C57BL/6J	N	22654668
MGI:5427980	M	MP:0002216	abnormal seminiferous tubule morphology	Katnal1<1H>/Katnal1<1H>	involves: C3H/HeH * C57BL/6J	N	22654668
MGI:5427980	M	MP:0001156	abnormal spermatogenesis	Katnal1<1H>/Katnal1<1H>	involves: C3H/HeH * C57BL/6J	N	22654668
MGI:5427980	M	MP:0004852	decreased testis weight	Katnal1<1H>/Katnal1<1H>	involves: C3H/HeH * C57BL/6J	N	22654668
MGI:5427980	M	MP:0006380	abnormal spermatid morphology	Katnal1<1H>/Katnal1<1H>	involves: C3H/HeH * C57BL/6J	N	22654668
MGI:5427980	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Katnal1<1H>/Katnal1<1H>	involves: C3H/HeH * C57BL/6J	N	22654668
MGI:5427994	F	MP:0002169	no abnormal phenotype detected	Tmsb4x<tm1Chen>/Tmsb4x<tm1Chen>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	22158707
MGI:5427997	F	MP:0005385	cardiovascular system phenotype	Tmsb4x<tm1.1Chen>/Tmsb4x<tm1.1Chen>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	Y	22158707
MGI:5427997	F	MP:0002169	no abnormal phenotype detected	Tmsb4x<tm1.1Chen>/Tmsb4x<tm1.1Chen>	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	22158707
MGI:5427998	M	MP:0005385	cardiovascular system phenotype	Tmsb4x<tm1.1Chen>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	Y	22158707
MGI:5427998	M	MP:0002169	no abnormal phenotype detected	Tmsb4x<tm1.1Chen>/Y	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	22158707
MGI:5428018	M	MP:0002169	no abnormal phenotype detected	Tmsb4x<tm1.2Chen>/Y,Tg(Nkx2-5-cre)9Eno/0	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	22158707
MGI:5428019	M	MP:0002169	no abnormal phenotype detected	Tmsb4x<tm1.2Chen>/Y,Tg(Myhca-cre)1Abel/0	involves: 129S1/Sv * 129X1/SvJ * Black Swiss	N	22158707
MGI:5428021	M	MP:0001925	male infertility	Fam20c<tm1.1Cqi>/Fam20c<tm1.1Cqi>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	22615579
MGI:5428021	F	MP:0001926	female infertility	Fam20c<tm1.1Cqi>/Fam20c<tm1.1Cqi>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	22615579
MGI:5428218	F	MP:0010024	increased total body fat amount	Ccl25<tm1Lex>/Ccl25<tm1Lex>	B6;129S5-Ccl25<tm1Lex>/Ieg	N	21421850
MGI:5428218	F	MP:0010024	increased total body fat amount	Ccl25<tm1Lex>/Ccl25<tm1Lex>	B6;129S5-Ccl25<tm1Lex>/Ieg	N	MGI:2655403
MGI:5428305	F	MP:0005179	decreased circulating cholesterol level	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	B6;129S5-Elovl6<Gt(OST222498)Lex>/Orl	N	MGI:2655403
MGI:5428425	F	MP:0002078	abnormal glucose homeostasis	Hprt1<tm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno>/Hprt1<+>,Tg(PSEN1)5Dbo/0	involves: 129P2/OlaHsd	N	22096518
MGI:5428425	F	MP:0002063	abnormal learning/memory/conditioning	Hprt1<tm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno>/Hprt1<+>,Tg(PSEN1)5Dbo/0	involves: 129P2/OlaHsd	N	22096518
MGI:5428425	F	MP:0014365	impaired short-term object recognition memory	Hprt1<tm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno>/Hprt1<+>,Tg(PSEN1)5Dbo/0	involves: 129P2/OlaHsd	N	22096518
MGI:5428425	F	MP:0001516	abnormal motor coordination/balance	Hprt1<tm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno>/Hprt1<+>,Tg(PSEN1)5Dbo/0	involves: 129P2/OlaHsd	N	22096518
MGI:5428425	F	MP:0001399	hyperactivity	Hprt1<tm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno>/Hprt1<+>,Tg(PSEN1)5Dbo/0	involves: 129P2/OlaHsd	N	22096518
MGI:5428425	F	MP:0002207	abnormal long-term potentiation	Hprt1<tm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno>/Hprt1<+>,Tg(PSEN1)5Dbo/0	involves: 129P2/OlaHsd	N	22096518
MGI:5428425	F	MP:0004994	abnormal brain wave pattern	Hprt1<tm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno>/Hprt1<+>,Tg(PSEN1)5Dbo/0	involves: 129P2/OlaHsd	N	22096518
MGI:5428425	F	MP:0009436	fragmentation of sleep/wake states	Hprt1<tm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno>/Hprt1<+>,Tg(PSEN1)5Dbo/0	involves: 129P2/OlaHsd	N	22096518
MGI:5428425	F	MP:0008428	abnormal spatial working memory	Hprt1<tm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno>/Hprt1<+>,Tg(PSEN1)5Dbo/0	involves: 129P2/OlaHsd	N	22096518
MGI:5428425	F	MP:0003631	nervous system phenotype	Hprt1<tm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno>/Hprt1<+>,Tg(PSEN1)5Dbo/0	involves: 129P2/OlaHsd	Y	22096518
MGI:5428425	F	MP:0002920	decreased paired-pulse facilitation	Hprt1<tm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno>/Hprt1<+>,Tg(PSEN1)5Dbo/0	involves: 129P2/OlaHsd	N	22096518
MGI:5428425	F	MP:0008414	abnormal spatial reference memory	Hprt1<tm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno>/Hprt1<+>,Tg(PSEN1)5Dbo/0	involves: 129P2/OlaHsd	N	22096518
MGI:5428426	F	MP:0010025	decreased total body fat amount	Gtf2ird1<tm1Hrd>/Gtf2ird1<tm1Hrd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22198572
MGI:5428426	F	MP:0001402	decreased locomotor activity	Gtf2ird1<tm1Hrd>/Gtf2ird1<tm1Hrd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22198572
MGI:5428426	F	MP:0004811	abnormal neuron physiology	Gtf2ird1<tm1Hrd>/Gtf2ird1<tm1Hrd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22198572
MGI:5428426	F	MP:0001745	increased circulating corticosterone level	Gtf2ird1<tm1Hrd>/Gtf2ird1<tm1Hrd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22198572
MGI:5428426	M	MP:0001399	hyperactivity	Gtf2ird1<tm1Hrd>/Gtf2ird1<tm1Hrd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22198572
MGI:5428433	M	MP:0003982	increased cholesterol level	Galr3<tm1Lex>/Galr3<tm1Lex>	B6;129S5-Galr3<tm1Lex>/Orl	N	MGI:2655403
MGI:5428433	M	MP:0005317	increased triglyceride level	Galr3<tm1Lex>/Galr3<tm1Lex>	B6;129S5-Galr3<tm1Lex>/Orl	N	MGI:2655403
MGI:5428677	M	MP:0001552	increased circulating triglyceride level	Il25<tm1Lex>/Il25<tm1Lex>	B6;129S5-Il25<tm1Lex>/Orl	N	MGI:2655403
MGI:5428678	M	MP:0003982	increased cholesterol level	Ilkap<Gt(OST55141)Lex>/Ilkap<Gt(OST55141)Lex>	B6;129S5-Ilkap<Gt(OST55141)Lex>/Ieg	N	MGI:2655403
MGI:5428692	F	MP:0011353	expanded mesangial matrix	Hprt1<tm1(Nphs1-CMIP)Dsah>/Hprt1<+>	B6.Cg-Hprt1<tm1(Nphs1-CMIP)Dsah>	N	20484117
MGI:5428692	F	MP:0008061	absent podocyte slit diaphragm	Hprt1<tm1(Nphs1-CMIP)Dsah>/Hprt1<+>	B6.Cg-Hprt1<tm1(Nphs1-CMIP)Dsah>	N	20484117
MGI:5428692	F	MP:0008060	abnormal podocyte slit diaphragm morphology	Hprt1<tm1(Nphs1-CMIP)Dsah>/Hprt1<+>	B6.Cg-Hprt1<tm1(Nphs1-CMIP)Dsah>	N	20484117
MGI:5428692	F	MP:0008140	podocyte foot process effacement	Hprt1<tm1(Nphs1-CMIP)Dsah>/Hprt1<+>	B6.Cg-Hprt1<tm1(Nphs1-CMIP)Dsah>	N	20484117
MGI:5428692	F	MP:0002871	albuminuria	Hprt1<tm1(Nphs1-CMIP)Dsah>/Hprt1<+>	B6.Cg-Hprt1<tm1(Nphs1-CMIP)Dsah>	N	20484117
MGI:5428692	F	MP:0005326	abnormal podocyte morphology	Hprt1<tm1(Nphs1-CMIP)Dsah>/Hprt1<+>	B6.Cg-Hprt1<tm1(Nphs1-CMIP)Dsah>	N	20484117
MGI:5428692	F	MP:0002962	increased urine protein level	Hprt1<tm1(Nphs1-CMIP)Dsah>/Hprt1<+>	B6.Cg-Hprt1<tm1(Nphs1-CMIP)Dsah>	N	20484117
MGI:5428692	F	MP:0011427	increased mesangial cell number	Hprt1<tm1(Nphs1-CMIP)Dsah>/Hprt1<+>	B6.Cg-Hprt1<tm1(Nphs1-CMIP)Dsah>	N	20484117
MGI:5428692	F	MP:0005264	glomerulosclerosis	Hprt1<tm1(Nphs1-CMIP)Dsah>/Hprt1<+>	B6.Cg-Hprt1<tm1(Nphs1-CMIP)Dsah>	N	20484117
MGI:5428701	M	MP:0010024	increased total body fat amount	Rras2<Gt(OST47398)Lex>/Rras2<Gt(OST47398)Lex>	B6;129S5-Rras2<Gt(OST47398)Lex>/Ieg	N	MGI:2655403
MGI:5428701	M	MP:0001264	increased body size	Rras2<Gt(OST47398)Lex>/Rras2<Gt(OST47398)Lex>	B6;129S5-Rras2<Gt(OST47398)Lex>/Ieg	N	MGI:2655403
MGI:5428739	F	MP:0000752	dystrophic muscle	Dmd<mdx>/Dmd<mdx>,Tg(ACTA1-SSPN)3.0Rcros/0	involves: C57BL/10ScSn	N	22734004
MGI:5428739	F	MP:0004121	abnormal sarcolemma morphology	Dmd<mdx>/Dmd<mdx>,Tg(ACTA1-SSPN)3.0Rcros/0	involves: C57BL/10ScSn	N	22734004
MGI:5428739	F	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<mdx>/Dmd<mdx>,Tg(ACTA1-SSPN)3.0Rcros/0	involves: C57BL/10ScSn	N	22734004
MGI:5428763	M	MP:0009852	increased Sertoli cell phagocytosis	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0031352	absent sperm axonemal central pair	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0002675	asthenozoospermia	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0002686	globozoospermia	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0001147	small testis	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0031356	abnormal outer dense fiber morphology	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0005389	reproductive system phenotype	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	Y	22654669
MGI:5428763	M	MP:0031373	abnormal manchette perinuclear ring morphology	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0001925	male infertility	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0020451	decreased sperm progressive motility	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0005169	abnormal male meiosis	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0031386	elongated manchette	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0008892	abnormal sperm flagellum morphology	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0031375	abnormal manchette disassembly	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0002687	oligozoospermia	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0006380	abnormal spermatid morphology	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0009838	abnormal sperm axoneme morphology	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428763	M	MP:0009376	abnormal manchette morphology	Katnb1<taily>/Katnb1<taily>	involves: C57BL/6 * CBA	N	22654669
MGI:5428841	M	MP:0002631	abnormal epididymis morphology	Tg(Pklr-HRAS*G12V)21Ak/0	involves: C57BL/6 * DBA/2	N	9398057
MGI:5428841	M	MP:0001925	male infertility	Tg(Pklr-HRAS*G12V)21Ak/0	involves: C57BL/6 * DBA/2	N	9398057
MGI:5428841	M	MP:0004931	enlarged epididymis	Tg(Pklr-HRAS*G12V)21Ak/0	involves: C57BL/6 * DBA/2	N	9398057
MGI:5428843	F	MP:0001926	female infertility	Marf1<Gt(AS0671)Wtsi>/Marf1<Gt(AS0671)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	22442484
MGI:5428844	F	MP:0001926	female infertility	Marf1<Gt(AS0671)Wtsi>/Marf1<m1Rpg>	involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J	N	22442484
MGI:5428871	M	MP:0001577	anemia	Gpc4<tm1Lex>/Y	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:3510987
MGI:5428877	M	MP:0003961	decreased lean body mass	Cnih1<Gt(OST237199)Lex>/Cnih1<Gt(OST237199)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	20562862
MGI:5428877	M	MP:0001262	decreased body weight	Cnih1<Gt(OST237199)Lex>/Cnih1<Gt(OST237199)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	20562862
MGI:5428877	M	MP:0001364	decreased anxiety-related response	Cnih1<Gt(OST237199)Lex>/Cnih1<Gt(OST237199)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	20562862
MGI:5428928	F	MP:0011703	increased fibroblast proliferation	Acp1<tm1Lex>/Acp1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:5000289
MGI:5428928	M	MP:0001265	decreased body size	Acp1<tm1Lex>/Acp1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:5000289
MGI:5429078	F	MP:0005375	adipose tissue phenotype	Htr2c<tm2Lex>/Htr2c<tm2Lex>	involves: 129S5/SvEvBrd * C57BL/6J	Y	18719666
MGI:5429081	F	MP:0005458	increased percent body fat/body weight	Brs3<tm1Lex>/Brs3<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	18719666
MGI:5429182	F	MP:0005017	decreased B cell number	Atp11c<m2Btlr>/Atp11c<m2Btlr>	involves: C57BL/6J	N	22761313
MGI:5429182	F	MP:0005387	immune system phenotype	Atp11c<m2Btlr>/Atp11c<m2Btlr>	involves: C57BL/6J	Y	22761313
MGI:5429185	F	MP:0004816	abnormal class switch recombination	Cd40lg<m1Btlr>/Cd40lg<m1Btlr>	involves: C57BL/6J	N	22761313
MGI:5429185	F	MP:0005387	immune system phenotype	Cd40lg<m1Btlr>/Cd40lg<m1Btlr>	involves: C57BL/6J	Y	22761313
MGI:5429185	F	MP:0001805	decreased IgG level	Cd40lg<m1Btlr>/Cd40lg<m1Btlr>	involves: C57BL/6J	N	22761313
MGI:5429193	M	MP:0004816	abnormal class switch recombination	Cd40lg<m1Btlr>/Y	involves: C57BL/6J	N	22761313
MGI:5429193	M	MP:0005387	immune system phenotype	Cd40lg<m1Btlr>/Y	involves: C57BL/6J	Y	22761313
MGI:5429193	M	MP:0001805	decreased IgG level	Cd40lg<m1Btlr>/Y	involves: C57BL/6J	N	22761313
MGI:5429507	M	MP:0001363	increased anxiety-related response	Sppl3<Gt(OST279815)Lex>/Sppl3<Gt(OST279815)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	20562862
MGI:5429549	M	MP:0008893	detached sperm flagellum	Nme5<tm1Lex>/Nme5<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21746835
MGI:5429549	M	MP:0008892	abnormal sperm flagellum morphology	Nme5<tm1Lex>/Nme5<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21746835
MGI:5429549	M	MP:0006380	abnormal spermatid morphology	Nme5<tm1Lex>/Nme5<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21746835
MGI:5429549	M	MP:0005159	azoospermia	Nme5<tm1Lex>/Nme5<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21746835
MGI:5429549	M	MP:0001155	arrest of spermatogenesis	Nme5<tm1Lex>/Nme5<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21746835
MGI:5429551	F	MP:0001926	female infertility	Stk36<tm1Lex>/Stk36<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21746835
MGI:5429553	M	MP:0001925	male infertility	Ak7<Gt(OST434404)Lex>/Ak7<Gt(OST434404)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21746835
MGI:5429553	M	MP:0001155	arrest of spermatogenesis	Ak7<Gt(OST434404)Lex>/Ak7<Gt(OST434404)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21746835
MGI:5429553	M	MP:0002687	oligozoospermia	Ak7<Gt(OST434404)Lex>/Ak7<Gt(OST434404)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21746835
MGI:5429556	M	MP:0001925	male infertility	Pomk<Gt(OST243203)Lex>/Pomk<Gt(OST243203)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	21746835
MGI:5429565	M	MP:0014413	decreased depression-related behavior	Fam3d<tm1Lex>/Fam3d<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:5000289
MGI:5429565	M	MP:0001364	decreased anxiety-related response	Fam3d<tm1Lex>/Fam3d<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:5000289
MGI:5429579	F	MP:0005202	lethargy	Mecp2<tm1.1Irsf>/Mecp2<+>	involves: 129S/Sv * C57BL/6	N	MGI:5429571
MGI:5429579	F	MP:0001405	impaired coordination	Mecp2<tm1.1Irsf>/Mecp2<+>	involves: 129S/Sv * C57BL/6	N	MGI:5429571
MGI:5429579	F	MP:0001260	increased body weight	Mecp2<tm1.1Irsf>/Mecp2<+>	involves: 129S/Sv * C57BL/6	N	MGI:5429571
MGI:5429580	M	MP:0001513	limb grasping	Mecp2<tm1.1Irsf>/Y	involves: 129S/Sv * C57BL/6	N	MGI:5429571
MGI:5429580	M	MP:0001405	impaired coordination	Mecp2<tm1.1Irsf>/Y	involves: 129S/Sv * C57BL/6	N	MGI:5429571
MGI:5429580	M	MP:0001406	abnormal gait	Mecp2<tm1.1Irsf>/Y	involves: 129S/Sv * C57BL/6	N	MGI:5429571
MGI:5429580	M	MP:0001260	increased body weight	Mecp2<tm1.1Irsf>/Y	involves: 129S/Sv * C57BL/6	N	MGI:5429571
MGI:5429726	M	MP:0002398	abnormal bone marrow cell morphology/development	Dp(16Cbr1-Fam3b)1Rhr/0,Gata1<tm8.2Sho>/Y	involves: 129S1/Sv * 129S6/SvEvTac	N	22354171
MGI:5429726	M	MP:0002413	abnormal megakaryocyte progenitor cell morphology	Dp(16Cbr1-Fam3b)1Rhr/0,Gata1<tm8.2Sho>/Y	involves: 129S1/Sv * 129S6/SvEvTac	N	22354171
MGI:5429726	M	MP:0000172	abnormal bone marrow cell number	Dp(16Cbr1-Fam3b)1Rhr/0,Gata1<tm8.2Sho>/Y	involves: 129S1/Sv * 129S6/SvEvTac	N	22354171
MGI:5429726	M	MP:0000691	enlarged spleen	Dp(16Cbr1-Fam3b)1Rhr/0,Gata1<tm8.2Sho>/Y	involves: 129S1/Sv * 129S6/SvEvTac	N	22354171
MGI:5429726	M	MP:0000220	increased monocyte cell number	Dp(16Cbr1-Fam3b)1Rhr/0,Gata1<tm8.2Sho>/Y	involves: 129S1/Sv * 129S6/SvEvTac	N	22354171
MGI:5429726	M	MP:0005505	thrombocytosis	Dp(16Cbr1-Fam3b)1Rhr/0,Gata1<tm8.2Sho>/Y	involves: 129S1/Sv * 129S6/SvEvTac	N	22354171
MGI:5429726	M	MP:0008254	increased megakaryocyte cell number	Dp(16Cbr1-Fam3b)1Rhr/0,Gata1<tm8.2Sho>/Y	involves: 129S1/Sv * 129S6/SvEvTac	N	22354171
MGI:5429726	M	MP:0001577	anemia	Dp(16Cbr1-Fam3b)1Rhr/0,Gata1<tm8.2Sho>/Y	involves: 129S1/Sv * 129S6/SvEvTac	N	22354171
MGI:5429726	M	MP:0000240	extramedullary hematopoiesis	Dp(16Cbr1-Fam3b)1Rhr/0,Gata1<tm8.2Sho>/Y	involves: 129S1/Sv * 129S6/SvEvTac	N	22354171
MGI:5429853	F	MP:0002680	decreased corpora lutea number	Akt2<tm1Hem>/Akt2<tm1Hem>	involves: 129P2/OlaHsd	N	22275470
MGI:5429853	F	MP:0009371	increased theca cell number	Akt2<tm1Hem>/Akt2<tm1Hem>	involves: 129P2/OlaHsd	N	22275470
MGI:5429853	F	MP:0002016	ovary cyst	Akt2<tm1Hem>/Akt2<tm1Hem>	involves: 129P2/OlaHsd	N	22275470
MGI:5429853	F	MP:0001126	abnormal ovary morphology	Akt2<tm1Hem>/Akt2<tm1Hem>	involves: 129P2/OlaHsd	N	22275470
MGI:5429859	M	MP:0030978	impaired binding of sperm to zona pellucida	Pmis2<tm1Osb>/Pmis2<tm1Osb>	involves: 129 * C57BL/6	N	22621904
MGI:5429859	M	MP:0003698	abnormal male reproductive system physiology	Pmis2<tm1Osb>/Pmis2<tm1Osb>	involves: 129 * C57BL/6	N	22621904
MGI:5429859	M	MP:0001925	male infertility	Pmis2<tm1Osb>/Pmis2<tm1Osb>	involves: 129 * C57BL/6	N	22621904
MGI:5429859	M	MP:0031012	impaired sperm migration in female genital tract	Pmis2<tm1Osb>/Pmis2<tm1Osb>	involves: 129 * C57BL/6	N	22621904
MGI:5430225	M	MP:0001925	male infertility	Vangl2<Lp>/Vangl2<Lp>	B6.A(Cg)-Vangl2<Lp>	N	22363783
MGI:5430225	F	MP:0001144	vagina atresia	Vangl2<Lp>/Vangl2<Lp>	B6.A(Cg)-Vangl2<Lp>	N	22363783
MGI:5430387	F	MP:0005379	endocrine/exocrine gland phenotype	Hs2st1<tm1.1Je>/Hs2st1<tm1.1Je>,Hs6st1<tm1Wvc>/Hs6st1<tm1Wvc>,Hs6st2<tm1Lex>/Hs6st2<tm1Lex>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129 * C57BL/6J * CBA/J	Y	22745308
MGI:5430593	M	MP:0001922	reduced male fertility	Tg(Dyrk1a)189N3Yah/0	B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	N	34828406
MGI:5430593	M	MP:0002216	abnormal seminiferous tubule morphology	Tg(Dyrk1a)189N3Yah/0	B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	N	34828406
MGI:5430593	M	MP:0006378	abnormal spermatogonia morphology	Tg(Dyrk1a)189N3Yah/0	B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	N	34828406
MGI:5430593	M	MP:0009819	abnormal circulating androgen level	Tg(Dyrk1a)189N3Yah/0	B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	N	34828406
MGI:5430593	M	MP:0003953	abnormal hormone level	Tg(Dyrk1a)189N3Yah/0	B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	N	34828406
MGI:5430593	M	MP:0002773	decreased circulating luteinizing hormone level	Tg(Dyrk1a)189N3Yah/0	B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	N	34828406
MGI:5430593	M	MP:0004852	decreased testis weight	Tg(Dyrk1a)189N3Yah/0	B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	N	34828406
MGI:5430593	M	MP:0002780	decreased circulating testosterone level	Tg(Dyrk1a)189N3Yah/0	B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	N	34828406
MGI:5430593	M	MP:0002687	oligozoospermia	Tg(Dyrk1a)189N3Yah/0	B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	N	34828406
MGI:5430593	M	MP:0001155	arrest of spermatogenesis	Tg(Dyrk1a)189N3Yah/0	B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	N	34828406
MGI:5430593	M	MP:0002790	decreased circulating follicle stimulating hormone level	Tg(Dyrk1a)189N3Yah/0	B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	N	34828406
MGI:5430593	M	MP:0003363	decreased circulating gonadotropin level	Tg(Dyrk1a)189N3Yah/0	B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	N	34828406
MGI:5430593	M	MP:0005319	abnormal enzyme/coenzyme level	Tg(Dyrk1a)189N3Yah/0	B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	N	34828406
MGI:5430606	M	MP:0020550	multinucleated giant male germ cells	Tas1r1<tm1Uboe>/Tas1r1<tm1Uboe>	involves: C57BL/6	N	22427794
MGI:5430606	M	MP:0014052	increased male germ cell apoptosis	Tas1r1<tm1Uboe>/Tas1r1<tm1Uboe>	involves: C57BL/6	N	22427794
MGI:5430606	M	MP:0004543	abnormal sperm physiology	Tas1r1<tm1Uboe>/Tas1r1<tm1Uboe>	involves: C57BL/6	N	22427794
MGI:5430606	M	MP:0013288	premature acrosome reaction	Tas1r1<tm1Uboe>/Tas1r1<tm1Uboe>	involves: C57BL/6	N	22427794
MGI:5430606	M	MP:0002216	abnormal seminiferous tubule morphology	Tas1r1<tm1Uboe>/Tas1r1<tm1Uboe>	involves: C57BL/6	N	22427794
MGI:5430606	M	MP:0001156	abnormal spermatogenesis	Tas1r1<tm1Uboe>/Tas1r1<tm1Uboe>	involves: C57BL/6	N	22427794
MGI:5430751	F	MP:0001262	decreased body weight	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Ocrl<tm1Nbm>,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430751	F	MP:0002083	premature death	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Ocrl<tm1Nbm>,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430751	F	MP:0009703	decreased birth body size	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Ocrl<tm1Nbm>,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430751	F	MP:0001732	postnatal growth retardation	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Ocrl<tm1Nbm>,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430751	F	MP:0003311	aminoaciduria	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Ocrl<tm1Nbm>,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430751	F	MP:0011555	increased urine microglobulin level	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Ocrl<tm1Nbm>,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430751	F	MP:0005391	vision/eye phenotype	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Ocrl<tm1Nbm>,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	Y	21183592
MGI:5430752	M	MP:0002083	premature death	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Y,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430752	M	MP:0003311	aminoaciduria	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Y,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430752	M	MP:0005391	vision/eye phenotype	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Y,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	Y	21183592
MGI:5430752	M	MP:0001262	decreased body weight	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Y,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430752	M	MP:0009703	decreased birth body size	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Y,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430752	M	MP:0001732	postnatal growth retardation	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Y,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430752	M	MP:0011555	increased urine microglobulin level	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Y,Tg(INPP5B)CNbm/0	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430753	F	MP:0001262	decreased body weight	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Ocrl<tm1Nbm>,Tg(INPP5B)CNbm/Tg(INPP5B)CNbm	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430753	F	MP:0001732	postnatal growth retardation	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Ocrl<tm1Nbm>,Tg(INPP5B)CNbm/Tg(INPP5B)CNbm	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430753	F	MP:0005367	renal/urinary system phenotype	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Ocrl<tm1Nbm>,Tg(INPP5B)CNbm/Tg(INPP5B)CNbm	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	Y	21183592
MGI:5430754	M	MP:0001262	decreased body weight	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Y,Tg(INPP5B)CNbm/Tg(INPP5B)CNbm	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430754	M	MP:0001732	postnatal growth retardation	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Y,Tg(INPP5B)CNbm/Tg(INPP5B)CNbm	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	N	21183592
MGI:5430754	M	MP:0005367	renal/urinary system phenotype	Inpp5b<tm1Nbm>/Inpp5b<tm1Nbm>,Ocrl<tm1Nbm>/Y,Tg(INPP5B)CNbm/Tg(INPP5B)CNbm	involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	Y	21183592
MGI:5430757	M	MP:0001156	abnormal spermatogenesis	Phf13<Gt(XB691)Byg>/Phf13<Gt(XB691)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21852425
MGI:5430757	M	MP:0008280	abnormal male germ cell apoptosis	Phf13<Gt(XB691)Byg>/Phf13<Gt(XB691)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21852425
MGI:5430757	M	MP:0002216	abnormal seminiferous tubule morphology	Phf13<Gt(XB691)Byg>/Phf13<Gt(XB691)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21852425
MGI:5430757	M	MP:0002687	oligozoospermia	Phf13<Gt(XB691)Byg>/Phf13<Gt(XB691)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21852425
MGI:5430757	M	MP:0001922	reduced male fertility	Phf13<Gt(XB691)Byg>/Phf13<Gt(XB691)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21852425
MGI:5430757	M	MP:0004852	decreased testis weight	Phf13<Gt(XB691)Byg>/Phf13<Gt(XB691)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21852425
MGI:5430757	M	MP:0003205	testicular atrophy	Phf13<Gt(XB691)Byg>/Phf13<Gt(XB691)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21852425
MGI:5430757	M	MP:0001147	small testis	Phf13<Gt(XB691)Byg>/Phf13<Gt(XB691)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21852425
MGI:5430758	M	MP:0001156	abnormal spermatogenesis	Phf13<Gt(XB691)Byg>/Phf13<Gt(XB691)Byg>	B6.129P2-Phf13<Gt(XB691)Byg>	N	21852425
MGI:5430759	M	MP:0003698	abnormal male reproductive system physiology	Phf13<Gt(XA022)Byg>/Phf13<Gt(XA022)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21852425
MGI:5430759	M	MP:0001145	abnormal male reproductive system morphology	Phf13<Gt(XA022)Byg>/Phf13<Gt(XA022)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	21852425
MGI:5430767	M	MP:0001922	reduced male fertility	Ephb6/Trpv6<tm1.1Mfre>/Ephb6/Trpv6<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N	N	21540454
MGI:5430767	M	MP:0002675	asthenozoospermia	Ephb6/Trpv6<tm1.1Mfre>/Ephb6/Trpv6<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N	N	21540454
MGI:5430767	M	MP:0004933	abnormal epididymis epithelium morphology	Ephb6/Trpv6<tm1.1Mfre>/Ephb6/Trpv6<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N	N	21540454
MGI:5430767	M	MP:0009325	necrospermia	Ephb6/Trpv6<tm1.1Mfre>/Ephb6/Trpv6<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N	N	21540454
MGI:5430773	M	MP:0004933	abnormal epididymis epithelium morphology	Ephb6/Trpv6<tm1.1Mfre>/Ephb6/Trpv6<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N	N	21540454
MGI:5430773	M	MP:0002675	asthenozoospermia	Ephb6/Trpv6<tm1.1Mfre>/Ephb6/Trpv6<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N	N	21540454
MGI:5430773	M	MP:0009325	necrospermia	Ephb6/Trpv6<tm1.1Mfre>/Ephb6/Trpv6<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N	N	21540454
MGI:5430773	M	MP:0001922	reduced male fertility	Ephb6/Trpv6<tm1.1Mfre>/Ephb6/Trpv6<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N	N	21540454
MGI:5430787	M	MP:0001158	abnormal prostate gland morphology	Del(6Ephb6-Trpv6)2Mfre/Del(6Ephb6-Trpv6)2Mfre	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	22427671
MGI:5430787	M	MP:0009734	abnormal prostate gland duct morphology	Del(6Ephb6-Trpv6)2Mfre/Del(6Ephb6-Trpv6)2Mfre	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	22427671
MGI:5430787	M	MP:0001922	reduced male fertility	Del(6Ephb6-Trpv6)2Mfre/Del(6Ephb6-Trpv6)2Mfre	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	22427671
MGI:5430787	M	MP:0004933	abnormal epididymis epithelium morphology	Del(6Ephb6-Trpv6)2Mfre/Del(6Ephb6-Trpv6)2Mfre	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	22427671
MGI:5430787	M	MP:0001168	abnormal prostate gland epithelium morphology	Del(6Ephb6-Trpv6)2Mfre/Del(6Ephb6-Trpv6)2Mfre	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	22427671
MGI:5430787	M	MP:0002675	asthenozoospermia	Del(6Ephb6-Trpv6)2Mfre/Del(6Ephb6-Trpv6)2Mfre	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	22427671
MGI:5430787	M	MP:0009325	necrospermia	Del(6Ephb6-Trpv6)2Mfre/Del(6Ephb6-Trpv6)2Mfre	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	22427671
MGI:5430793	F	MP:0001727	abnormal embryo implantation	Itgb1<tm13.1Ref>/Itgb1<tm13.1Ref>	involves: 129S1/Sv * 129X1/SvJ	N	22561348
MGI:5430938	F	MP:0002644	decreased circulating triglyceride level	Nxph4<tm1Lex>/Nxph4<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:5000289
MGI:5430944	M	MP:0002675	asthenozoospermia	Pip5k1a<tm1.1Tba>/Pip5k1a<tm1.1Tba>	involves: 129P2/OlaHsd	N	22321832
MGI:5430944	M	MP:0009831	abnormal sperm midpiece morphology	Pip5k1a<tm1.1Tba>/Pip5k1a<tm1.1Tba>	involves: 129P2/OlaHsd	N	22321832
MGI:5430944	M	MP:0001922	reduced male fertility	Pip5k1a<tm1.1Tba>/Pip5k1a<tm1.1Tba>	involves: 129P2/OlaHsd	N	22321832
MGI:5430945	M	MP:0009238	coiled sperm flagellum	Pip5k1a<tm1.1Tba>/Pip5k1a<tm1.1Tba>,Pip5k1b<tm1Tssk>/Pip5k1b<tm1Tssk>	involves: 129P2/OlaHsd	N	22321832
MGI:5430945	M	MP:0001925	male infertility	Pip5k1a<tm1.1Tba>/Pip5k1a<tm1.1Tba>,Pip5k1b<tm1Tssk>/Pip5k1b<tm1Tssk>	involves: 129P2/OlaHsd	N	22321832
MGI:5430945	M	MP:0002675	asthenozoospermia	Pip5k1a<tm1.1Tba>/Pip5k1a<tm1.1Tba>,Pip5k1b<tm1Tssk>/Pip5k1b<tm1Tssk>	involves: 129P2/OlaHsd	N	22321832
MGI:5430945	M	MP:0004852	decreased testis weight	Pip5k1a<tm1.1Tba>/Pip5k1a<tm1.1Tba>,Pip5k1b<tm1Tssk>/Pip5k1b<tm1Tssk>	involves: 129P2/OlaHsd	N	22321832
MGI:5430945	M	MP:0002687	oligozoospermia	Pip5k1a<tm1.1Tba>/Pip5k1a<tm1.1Tba>,Pip5k1b<tm1Tssk>/Pip5k1b<tm1Tssk>	involves: 129P2/OlaHsd	N	22321832
MGI:5430945	M	MP:0009831	abnormal sperm midpiece morphology	Pip5k1a<tm1.1Tba>/Pip5k1a<tm1.1Tba>,Pip5k1b<tm1Tssk>/Pip5k1b<tm1Tssk>	involves: 129P2/OlaHsd	N	22321832
MGI:5430945	M	MP:0004182	abnormal spermiation	Pip5k1a<tm1.1Tba>/Pip5k1a<tm1.1Tba>,Pip5k1b<tm1Tssk>/Pip5k1b<tm1Tssk>	involves: 129P2/OlaHsd	N	22321832
MGI:5430945	M	MP:0008893	detached sperm flagellum	Pip5k1a<tm1.1Tba>/Pip5k1a<tm1.1Tba>,Pip5k1b<tm1Tssk>/Pip5k1b<tm1Tssk>	involves: 129P2/OlaHsd	N	22321832
MGI:5430999	F	MP:0001926	female infertility	Prkra<rep>/Prkra<rep>	involves: C3HeB/FeJ * C57BL/6J	N	22194846
MGI:5431005	M	MP:0001925	male infertility	Ak7<Tg(tetO-Hmox1)67Sami>/Ak7<Tg(tetO-Hmox1)67Sami>	FVB/N-Ak7<Tg(tetO-Hmox1)67Sami>	N	18776131
MGI:5431005	M	MP:0005159	azoospermia	Ak7<Tg(tetO-Hmox1)67Sami>/Ak7<Tg(tetO-Hmox1)67Sami>	FVB/N-Ak7<Tg(tetO-Hmox1)67Sami>	N	18776131
MGI:5431005	M	MP:0009230	abnormal sperm head morphology	Ak7<Tg(tetO-Hmox1)67Sami>/Ak7<Tg(tetO-Hmox1)67Sami>	FVB/N-Ak7<Tg(tetO-Hmox1)67Sami>	N	18776131
MGI:5431130	F	MP:0002016	ovary cyst	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	F	MP:0005431	decreased oocyte number	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	M	MP:0006379	abnormal spermatocyte morphology	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	F	MP:0011121	decreased primordial ovarian follicle number	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	M	MP:0003205	testicular atrophy	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	M	MP:0004901	decreased male germ cell number	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	F	MP:0005168	abnormal female meiosis	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	M	MP:0008261	arrest of male meiosis	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	F	MP:0001923	reduced female fertility	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	F	MP:0001126	abnormal ovary morphology	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	M	MP:0004852	decreased testis weight	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	M	MP:0001146	abnormal testis morphology	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	M	MP:0001153	small seminiferous tubules	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	M	MP:0005159	azoospermia	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	F	MP:0002680	decreased corpora lutea number	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	M	MP:0001925	male infertility	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	M	MP:0014052	increased male germ cell apoptosis	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	M	MP:0001155	arrest of spermatogenesis	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	M	MP:0001156	abnormal spermatogenesis	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	F	MP:0031474	increased female germ cell apoptosis	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431130	M	MP:0006380	abnormal spermatid morphology	Zc3hc1<tm1.2Jduy>/Zc3hc1<tm1.2Jduy>	B6.129S6(Cg)-Zc3hc1<tm1.2Jduy>	N	22696294
MGI:5431239	M	MP:0001925	male infertility	Ttll1<Gt(OST372941)Lex>/Ttll1<Gt(OST372941)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	20442420
MGI:5431239	M	MP:0001156	abnormal spermatogenesis	Ttll1<Gt(OST372941)Lex>/Ttll1<Gt(OST372941)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	20442420
MGI:5431239	M	MP:0008893	detached sperm flagellum	Ttll1<Gt(OST372941)Lex>/Ttll1<Gt(OST372941)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	20442420
MGI:5431239	M	MP:0009234	absent sperm head	Ttll1<Gt(OST372941)Lex>/Ttll1<Gt(OST372941)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	20442420
MGI:5431239	M	MP:0009831	abnormal sperm midpiece morphology	Ttll1<Gt(OST372941)Lex>/Ttll1<Gt(OST372941)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	20442420
MGI:5431239	M	MP:0005578	teratozoospermia	Ttll1<Gt(OST372941)Lex>/Ttll1<Gt(OST372941)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	20442420
MGI:5431239	M	MP:0002687	oligozoospermia	Ttll1<Gt(OST372941)Lex>/Ttll1<Gt(OST372941)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	20442420
MGI:5431239	M	MP:0020869	immotile sperm	Ttll1<Gt(OST372941)Lex>/Ttll1<Gt(OST372941)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	20442420
MGI:5431239	M	MP:0008545	absent sperm flagellum	Ttll1<Gt(OST372941)Lex>/Ttll1<Gt(OST372941)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	20442420
MGI:5431915	F	MP:0009298	increased mesenteric fat pad weight	Csf2<tm1Mlg>/Csf2<tm1Mlg>	B6.129S2-Csf2<tm1Mlg>	N	16276414
MGI:5431915	M	MP:0001552	increased circulating triglyceride level	Csf2<tm1Mlg>/Csf2<tm1Mlg>	B6.129S2-Csf2<tm1Mlg>	N	16276414
MGI:5431915	M	MP:0011939	increased food intake	Csf2<tm1Mlg>/Csf2<tm1Mlg>	B6.129S2-Csf2<tm1Mlg>	N	16276414
MGI:5431915	M	MP:0001554	increased circulating free fatty acids level	Csf2<tm1Mlg>/Csf2<tm1Mlg>	B6.129S2-Csf2<tm1Mlg>	N	16276414
MGI:5431943	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Rdp>/Pten<tm1Rdp>,Tert<tm1Rdp>/Tert<tm1Rdp>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22341455
MGI:5431944	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Rdp>/Pten<tm1Rdp>,Tert<tm1Rdp>/Tert<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22341455
MGI:5431944	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Rdp>/Pten<tm1Rdp>,Tert<tm1Rdp>/Tert<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22341455
MGI:5431945	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Rdp>/Pten<tm1Rdp>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22341455
MGI:5431945	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Rdp>/Pten<tm1Rdp>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22341455
MGI:5431947	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Rdp>/Pten<tm1Rdp>,Smad4<tm1Rdp>/Smad4<tm1Rdp>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129 * C57BL/6 * DBA/2	N	22341455
MGI:5431958	M	MP:0003871	abnormal myelin sheath morphology	Drp2<tm1.1Brp>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	22764250
MGI:5431958	M	MP:0003631	nervous system phenotype	Drp2<tm1.1Brp>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	Y	22764250
MGI:5431958	M	MP:0010742	increased Schwann cell number	Drp2<tm1.1Brp>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	22764250
MGI:5431958	M	MP:0001106	abnormal Schwann cell morphology	Drp2<tm1.1Brp>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	22764250
MGI:5431958	M	MP:0010050	hypermyelination	Drp2<tm1.1Brp>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	22764250
MGI:5431978	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Rdp>/Pten<tm1Rdp>,Tert<tm3Rdp>/Tert<tm3Rdp>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22341455
MGI:5431978	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Rdp>/Pten<tm1Rdp>,Tert<tm3Rdp>/Tert<tm3Rdp>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22341455
MGI:5431981	M	MP:0003205	testicular atrophy	Tert<tm3Rdp>/Tert<tm3Rdp>	involves: C57BL/6	N	22341455
MGI:5431981	M	MP:0004852	decreased testis weight	Tert<tm3Rdp>/Tert<tm3Rdp>	involves: C57BL/6	N	22341455
MGI:5432120	M	MP:0000230	abnormal systemic arterial blood pressure	Gucy1b1<tm1.2Frb>/Gucy1b1<tm1.2Frb>,X/Tg(Myh11-icre/ERT2)1Soff	B6.Cg-Gucy1b1<tm1.2Frb> Tg(Myh11-icre/ERT2)1Soff	N	20065162
MGI:5432120	M	MP:0000231	hypertension	Gucy1b1<tm1.2Frb>/Gucy1b1<tm1.2Frb>,X/Tg(Myh11-icre/ERT2)1Soff	B6.Cg-Gucy1b1<tm1.2Frb> Tg(Myh11-icre/ERT2)1Soff	N	20065162
MGI:5432120	M	MP:0005591	decreased vasodilation	Gucy1b1<tm1.2Frb>/Gucy1b1<tm1.2Frb>,X/Tg(Myh11-icre/ERT2)1Soff	B6.Cg-Gucy1b1<tm1.2Frb> Tg(Myh11-icre/ERT2)1Soff	N	20065162
MGI:5432120	M	MP:0006144	increased systemic arterial systolic blood pressure	Gucy1b1<tm1.2Frb>/Gucy1b1<tm1.2Frb>,X/Tg(Myh11-icre/ERT2)1Soff	B6.Cg-Gucy1b1<tm1.2Frb> Tg(Myh11-icre/ERT2)1Soff	N	20065162
MGI:5432223	F	MP:0008000	increased ovary tumor incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Tg(CYP19A1-cre)1Jri/0	involves: 129X1/SvJ * C57BL/6	N	21860425
MGI:5432224	F	MP:0001750	increased circulating follicle stimulating hormone level	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Kras<tm4Tyj>/Kras<+>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432224	F	MP:0005181	decreased circulating estradiol level	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Kras<tm4Tyj>/Kras<+>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432224	F	MP:0005185	decreased circulating progesterone level	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Kras<tm4Tyj>/Kras<+>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432224	F	MP:0001751	increased circulating luteinizing hormone level	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Kras<tm4Tyj>/Kras<+>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432224	F	MP:0012411	increased granulosa cell tumor incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Kras<tm4Tyj>/Kras<+>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432224	F	MP:0008000	increased ovary tumor incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Kras<tm4Tyj>/Kras<+>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432224	F	MP:0003357	impaired granulosa cell differentiation	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Kras<tm4Tyj>/Kras<+>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432226	F	MP:0008000	increased ovary tumor incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432226	F	MP:0012411	increased granulosa cell tumor incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432226	F	MP:0031016	decreased granulosa cell apoptosis	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432226	F	MP:0031019	increased granulosa cell proliferation	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432226	F	MP:0003357	impaired granulosa cell differentiation	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432228	M	MP:0003205	testicular atrophy	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ctnnb1<tm1Mmt>/Ctnnb1<+>	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432228	M	MP:0001154	seminiferous tubule degeneration	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ctnnb1<tm1Mmt>/Ctnnb1<+>	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432228	M	MP:0001925	male infertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ctnnb1<tm1Mmt>/Ctnnb1<+>	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432228	M	MP:0006262	increased testis tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ctnnb1<tm1Mmt>/Ctnnb1<+>	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432228	F	MP:0012411	increased granulosa cell tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ctnnb1<tm1Mmt>/Ctnnb1<+>	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432231	M	MP:0001154	seminiferous tubule degeneration	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Kras<tm4Tyj>/Kras<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432231	F	MP:0012411	increased granulosa cell tumor incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Kras<tm4Tyj>/Kras<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432231	M	MP:0006262	increased testis tumor incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Kras<tm4Tyj>/Kras<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432232	F	MP:0012411	increased granulosa cell tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ctnnb1<tm1Mmt>/Ctnnb1<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432232	M	MP:0006262	increased testis tumor incidence	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Ctnnb1<tm1Mmt>/Ctnnb1<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	21860425
MGI:5432250	F	MP:0010173	increased mammary gland epithelial cell proliferation	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-MYC)1Lach/0	involves: FVB	N	11175856
MGI:5432250	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-MYC)1Lach/0	involves: FVB	N	11175856
MGI:5432250	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-MYC)1Lach/0	involves: FVB	N	11175856
MGI:5432250	F	MP:0014126	increased mammary gland apoptosis	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-MYC)1Lach/0	involves: FVB	N	11175856
MGI:5432250	F	MP:0010299	increased mammary gland tumor incidence	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-MYC)1Lach/0	involves: FVB	N	18356293
MGI:5432250	F	MP:0010299	increased mammary gland tumor incidence	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-MYC)1Lach/0	involves: FVB	N	11175856
MGI:5432250	F	MP:0000630	mammary gland hyperplasia	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-MYC)1Lach/0	involves: FVB	N	11175856
MGI:5432250	F	MP:0009504	abnormal mammary gland epithelium morphology	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-MYC)1Lach/0	involves: FVB	N	11175856
MGI:5432258	F	MP:0009504	abnormal mammary gland epithelium morphology	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-IGF1R)1Ramo/0	involves: FVB	N	16953219
MGI:5432258	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-IGF1R)1Ramo/0	involves: FVB	N	16953219
MGI:5432258	F	MP:0000630	mammary gland hyperplasia	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-IGF1R)1Ramo/0	involves: FVB	N	16953219
MGI:5432258	F	MP:0000628	abnormal mammary gland development	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-IGF1R)1Ramo/0	involves: FVB	N	16953219
MGI:5432337	M	MP:0005159	azoospermia	T(7;19)145H/?	involves: 101/H * C3H/HeH	N	5958877
MGI:5432337	M	MP:0001925	male infertility	T(7;19)145H/?	involves: 101/H * C3H/HeH	N	5958877
MGI:5432337	M	MP:0004852	decreased testis weight	T(7;19)145H/?	involves: 101/H * C3H/HeH	N	5958877
MGI:5432337	F	MP:0001923	reduced female fertility	T(7;19)145H/?	involves: 101/H * C3H/HeH	N	5958877
MGI:5432337	M	MP:0008261	arrest of male meiosis	T(7;19)145H/?	involves: 101/H * C3H/HeH	N	5958877
MGI:5432491	M	MP:0005536	decreased Leydig cell number	Fam20c<tm1Lex>/Fam20c<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	22732358
MGI:5432528	M	MP:0002685	abnormal spermatogonia proliferation	Cirbp<tm1Jfuji>/Cirbp<tm1Jfuji>	B6.129S2-Cirbp<tm1Jfuji>	N	22711815
MGI:5432528	M	MP:0006378	abnormal spermatogonia morphology	Cirbp<tm1Jfuji>/Cirbp<tm1Jfuji>	B6.129S2-Cirbp<tm1Jfuji>	N	22711815
MGI:5432573	M	MP:0004852	decreased testis weight	Crisp4<tm1(icre)Mpo>/Crisp4<tm1(icre)Mpo>	involves: 129S7/SvEvBrd * C57BL/6	N	21865554
MGI:5432780	M	MP:0004851	increased testis weight	Slc14a2<tm1Raf>/Slc14a2<tm1Raf>	B6.129S6-Slc14a2<tm1Raf>	N	15829709
MGI:5433109	F	MP:0002169	no abnormal phenotype detected	Magt1<Gt(OST199678)Lex>/Magt1<Gt(OST199678)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	20562862
MGI:5433110	M	MP:0002169	no abnormal phenotype detected	Magt1<Gt(OST199678)Lex>/Y	involves: 129S5/SvEvBrd * C57BL/6	N	20562862
MGI:5433190	F	MP:0005560	decreased circulating glucose level	Senp2<Gt(OST66117)Lex>/Senp2<+>	B6;129S5-Senp2<Gt(OST66117)Lex>/Orl	N	MGI:2655403
MGI:5433296	M	MP:0001463	abnormal spatial learning	Fgf13<tm1Xuzh>/Y,Emx1<tm1(cre)Yql>/Emx1<+>	involves: 129S2/SvPas	N	22726441
MGI:5433296	M	MP:0009969	abnormal cerebral cortex pyramidal cell morphology	Fgf13<tm1Xuzh>/Y,Emx1<tm1(cre)Yql>/Emx1<+>	involves: 129S2/SvPas	N	22726441
MGI:5433296	M	MP:0001399	hyperactivity	Fgf13<tm1Xuzh>/Y,Emx1<tm1(cre)Yql>/Emx1<+>	involves: 129S2/SvPas	N	22726441
MGI:5433296	M	MP:0003360	abnormal depression-related behavior	Fgf13<tm1Xuzh>/Y,Emx1<tm1(cre)Yql>/Emx1<+>	involves: 129S2/SvPas	N	22726441
MGI:5433296	M	MP:0005404	abnormal axon morphology	Fgf13<tm1Xuzh>/Y,Emx1<tm1(cre)Yql>/Emx1<+>	involves: 129S2/SvPas	N	22726441
MGI:5433296	M	MP:0009456	impaired cued conditioning behavior	Fgf13<tm1Xuzh>/Y,Emx1<tm1(cre)Yql>/Emx1<+>	involves: 129S2/SvPas	N	22726441
MGI:5433296	M	MP:0001458	abnormal object recognition memory	Fgf13<tm1Xuzh>/Y,Emx1<tm1(cre)Yql>/Emx1<+>	involves: 129S2/SvPas	N	22726441
MGI:5433296	M	MP:0001363	increased anxiety-related response	Fgf13<tm1Xuzh>/Y,Emx1<tm1(cre)Yql>/Emx1<+>	involves: 129S2/SvPas	N	22726441
MGI:5433296	M	MP:0008428	abnormal spatial working memory	Fgf13<tm1Xuzh>/Y,Emx1<tm1(cre)Yql>/Emx1<+>	involves: 129S2/SvPas	N	22726441
MGI:5433296	M	MP:0002573	behavioral despair	Fgf13<tm1Xuzh>/Y,Emx1<tm1(cre)Yql>/Emx1<+>	involves: 129S2/SvPas	N	22726441
MGI:5433297	F	MP:0006009	abnormal neuronal migration	Fgf13<tm1Xuzh>/Fgf13<tm1Xuzh>	involves: 129	N	22726441
MGI:5433298	M	MP:0004098	abnormal cerebellar granule cell morphology	Fgf13<tm1Xuzh>/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129 * FVB/N	N	22726441
MGI:5433298	M	MP:0000807	abnormal hippocampus morphology	Fgf13<tm1Xuzh>/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129 * FVB/N	N	22726441
MGI:5433298	M	MP:0008948	decreased neuron number	Fgf13<tm1Xuzh>/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129 * FVB/N	N	22726441
MGI:5433298	M	MP:0000812	abnormal dentate gyrus morphology	Fgf13<tm1Xuzh>/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129 * FVB/N	N	22726441
MGI:5433298	M	MP:0008947	increased neuron number	Fgf13<tm1Xuzh>/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129 * FVB/N	N	22726441
MGI:5433298	M	MP:0001463	abnormal spatial learning	Fgf13<tm1Xuzh>/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129 * FVB/N	N	22726441
MGI:5433298	M	MP:0008428	abnormal spatial working memory	Fgf13<tm1Xuzh>/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129 * FVB/N	N	22726441
MGI:5433298	M	MP:0002882	abnormal neuron morphology	Fgf13<tm1Xuzh>/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129 * FVB/N	N	22726441
MGI:5433298	M	MP:0009969	abnormal cerebral cortex pyramidal cell morphology	Fgf13<tm1Xuzh>/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129 * FVB/N	N	22726441
MGI:5433299	F	MP:0001463	abnormal spatial learning	Fgf13<tm1Xuzh>/Fgf13<tm1Xuzh>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129 * FVB/N	N	22726441
MGI:5433299	F	MP:0002882	abnormal neuron morphology	Fgf13<tm1Xuzh>/Fgf13<tm1Xuzh>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129 * FVB/N	N	22726441
MGI:5433299	F	MP:0008428	abnormal spatial working memory	Fgf13<tm1Xuzh>/Fgf13<tm1Xuzh>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129 * FVB/N	N	22726441
MGI:5433310	F	MP:0009397	increased trophoblast giant cell number	Plac1<tm1(KOMP)Vlcg>/Plac1<tm1(KOMP)Vlcg>	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433310	F	MP:0012098	increased spongiotrophoblast size	Plac1<tm1(KOMP)Vlcg>/Plac1<tm1(KOMP)Vlcg>	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433310	F	MP:0004920	increased placenta weight	Plac1<tm1(KOMP)Vlcg>/Plac1<tm1(KOMP)Vlcg>	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433310	F	MP:0011085	postnatal lethality, complete penetrance	Plac1<tm1(KOMP)Vlcg>/Plac1<tm1(KOMP)Vlcg>	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433310	F	MP:0001712	abnormal placenta development	Plac1<tm1(KOMP)Vlcg>/Plac1<tm1(KOMP)Vlcg>	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433311	F	MP:0001712	abnormal placenta development	Plac1<tm1(KOMP)Vlcg>/Plac1<+>	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433311	F	MP:0004260	enlarged placenta	Plac1<tm1(KOMP)Vlcg>/Plac1<+>	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433311	F	MP:0004920	increased placenta weight	Plac1<tm1(KOMP)Vlcg>/Plac1<+>	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433311	F	MP:0001698	decreased embryo size	Plac1<tm1(KOMP)Vlcg>/Plac1<+>	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433311	F	MP:0012098	increased spongiotrophoblast size	Plac1<tm1(KOMP)Vlcg>/Plac1<+>	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433311	F	MP:0009397	increased trophoblast giant cell number	Plac1<tm1(KOMP)Vlcg>/Plac1<+>	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433311	F	MP:0008957	abnormal placenta junctional zone morphology	Plac1<tm1(KOMP)Vlcg>/Plac1<+>	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433311	F	MP:0003123	paternal imprinting	Plac1<tm1(KOMP)Vlcg>/Plac1<+>	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433312	M	MP:0011086	postnatal lethality, incomplete penetrance	Plac1<tm1(KOMP)Vlcg>/Y	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433312	M	MP:0012098	increased spongiotrophoblast size	Plac1<tm1(KOMP)Vlcg>/Y	C57BL/6N-Plac1<tm1(KOMP)Vlcg>	N	22729990
MGI:5433577	F	MP:0004834	ovary hemorrhage	Esr1<tm1.1Gust>/Esr1<tm1.1Gust>	B6.129X1-Esr1<tm1.1Gust>	N	22800760
MGI:5433577	F	MP:0001926	female infertility	Esr1<tm1.1Gust>/Esr1<tm1.1Gust>	B6.129X1-Esr1<tm1.1Gust>	N	22800760
MGI:5433577	F	MP:0001132	absent mature ovarian follicles	Esr1<tm1.1Gust>/Esr1<tm1.1Gust>	B6.129X1-Esr1<tm1.1Gust>	N	22800760
MGI:5433577	F	MP:0002016	ovary cyst	Esr1<tm1.1Gust>/Esr1<tm1.1Gust>	B6.129X1-Esr1<tm1.1Gust>	N	22800760
MGI:5433577	F	MP:0001134	absent corpus luteum	Esr1<tm1.1Gust>/Esr1<tm1.1Gust>	B6.129X1-Esr1<tm1.1Gust>	N	22800760
MGI:5433577	F	MP:0001121	uterus hypoplasia	Esr1<tm1.1Gust>/Esr1<tm1.1Gust>	B6.129X1-Esr1<tm1.1Gust>	N	22800760
MGI:5433577	F	MP:0000628	abnormal mammary gland development	Esr1<tm1.1Gust>/Esr1<tm1.1Gust>	B6.129X1-Esr1<tm1.1Gust>	N	22800760
MGI:5433577	F	MP:0005559	increased circulating glucose level	Esr1<tm1.1Gust>/Esr1<tm1.1Gust>	B6.129X1-Esr1<tm1.1Gust>	N	22800760
MGI:5433577	M	MP:0001925	male infertility	Esr1<tm1.1Gust>/Esr1<tm1.1Gust>	B6.129X1-Esr1<tm1.1Gust>	N	22800760
MGI:5433577	F	MP:0001261	obese	Esr1<tm1.1Gust>/Esr1<tm1.1Gust>	B6.129X1-Esr1<tm1.1Gust>	N	22800760
MGI:5433577	F	MP:0001260	increased body weight	Esr1<tm1.1Gust>/Esr1<tm1.1Gust>	B6.129X1-Esr1<tm1.1Gust>	N	22800760
MGI:5433620	M	MP:0001922	reduced male fertility	Emc10<Gt(OST181617)Lex>/Emc10<Gt(OST181617)Lex>	B6;129S5-Emc10<Gt(OST181617)Lex>/Mmucd	N	MGI:5000289
MGI:5433620	F	MP:0001363	increased anxiety-related response	Emc10<Gt(OST181617)Lex>/Emc10<Gt(OST181617)Lex>	B6;129S5-Emc10<Gt(OST181617)Lex>/Mmucd	N	MGI:5000289
MGI:5433620	M	MP:0005292	improved glucose tolerance	Emc10<Gt(OST181617)Lex>/Emc10<Gt(OST181617)Lex>	B6;129S5-Emc10<Gt(OST181617)Lex>/Mmucd	N	MGI:5000289
MGI:5433696	F	MP:0001923	reduced female fertility	Mut1045/Mut1045<+>	involves: 101/H * C3H/HeH	N	MGI:3044155
MGI:5433764	M	MP:0009237	kinked sperm flagellum	Gpx4<tm3Marc>/Gpx4<tm3Marc>	involves: 129P2/OlaHsd	N	19417079
MGI:5433764	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Gpx4<tm3Marc>/Gpx4<tm3Marc>	involves: 129P2/OlaHsd	N	19417079
MGI:5433764	M	MP:0009647	decreased fertilization frequency	Gpx4<tm3Marc>/Gpx4<tm3Marc>	involves: 129P2/OlaHsd	N	19417079
MGI:5433764	M	MP:0009230	abnormal sperm head morphology	Gpx4<tm3Marc>/Gpx4<tm3Marc>	involves: 129P2/OlaHsd	N	19417079
MGI:5433764	M	MP:0001925	male infertility	Gpx4<tm3Marc>/Gpx4<tm3Marc>	involves: 129P2/OlaHsd	N	19417079
MGI:5433764	M	MP:0009836	abnormal sperm principal piece morphology	Gpx4<tm3Marc>/Gpx4<tm3Marc>	involves: 129P2/OlaHsd	N	19417079
MGI:5433764	F	MP:0005389	reproductive system phenotype	Gpx4<tm3Marc>/Gpx4<tm3Marc>	involves: 129P2/OlaHsd	Y	19417079
MGI:5433764	M	MP:0000242	impaired fertilization	Gpx4<tm3Marc>/Gpx4<tm3Marc>	involves: 129P2/OlaHsd	N	19417079
MGI:5433851	M	MP:0001156	abnormal spermatogenesis	Cbx3<tm1Pbs>/Cbx3<tm1Pbs>	involves: 129	N	20423503
MGI:5433851	M	MP:0001925	male infertility	Cbx3<tm1Pbs>/Cbx3<tm1Pbs>	involves: 129	N	20423503
MGI:5433851	M	MP:0001147	small testis	Cbx3<tm1Pbs>/Cbx3<tm1Pbs>	involves: 129	N	20423503
MGI:5433851	F	MP:0005389	reproductive system phenotype	Cbx3<tm1Pbs>/Cbx3<tm1Pbs>	involves: 129	Y	20423503
MGI:5433851	M	MP:0002687	oligozoospermia	Cbx3<tm1Pbs>/Cbx3<tm1Pbs>	involves: 129	N	20423503
MGI:5433851	M	MP:0002216	abnormal seminiferous tubule morphology	Cbx3<tm1Pbs>/Cbx3<tm1Pbs>	involves: 129	N	20423503
MGI:5435288	M	MP:0013601	increased testis apoptosis	Galnt3<tcal>/Galnt3<tcal>	involves: C3H * C57BL/6J	N	22912827
MGI:5435288	M	MP:0005250	decreased Sertoli cell number	Galnt3<tcal>/Galnt3<tcal>	involves: C3H * C57BL/6J	N	22912827
MGI:5435288	M	MP:0002687	oligozoospermia	Galnt3<tcal>/Galnt3<tcal>	involves: C3H * C57BL/6J	N	22912827
MGI:5435288	M	MP:0002216	abnormal seminiferous tubule morphology	Galnt3<tcal>/Galnt3<tcal>	involves: C3H * C57BL/6J	N	22912827
MGI:5435288	M	MP:0001925	male infertility	Galnt3<tcal>/Galnt3<tcal>	involves: C3H * C57BL/6J	N	22912827
MGI:5435550	M	MP:0003109	short femur	Phex<Hpr>/Y	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435550	M	MP:0000063	decreased bone mineral density	Phex<Hpr>/Y	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435550	M	MP:0002968	increased circulating alkaline phosphatase level	Phex<Hpr>/Y	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435550	M	MP:0000137	abnormal vertebrae morphology	Phex<Hpr>/Y	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435550	M	MP:0000198	decreased circulating phosphate level	Phex<Hpr>/Y	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435550	M	MP:0008158	increased diameter of femur	Phex<Hpr>/Y	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435550	M	MP:0003795	abnormal bone structure	Phex<Hpr>/Y	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435551	F	MP:0002968	increased circulating alkaline phosphatase level	Phex<Hpr>/Phex<+>	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435551	F	MP:0000063	decreased bone mineral density	Phex<Hpr>/Phex<+>	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435551	F	MP:0003723	abnormal long bone morphology	Phex<Hpr>/Phex<+>	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435551	F	MP:0003795	abnormal bone structure	Phex<Hpr>/Phex<+>	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435551	F	MP:0004686	decreased length of long bones	Phex<Hpr>/Phex<+>	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435551	F	MP:0008158	increased diameter of femur	Phex<Hpr>/Phex<+>	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435551	F	MP:0000198	decreased circulating phosphate level	Phex<Hpr>/Phex<+>	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435551	F	MP:0003109	short femur	Phex<Hpr>/Phex<+>	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435551	F	MP:0000137	abnormal vertebrae morphology	Phex<Hpr>/Phex<+>	involves: C3H/HeH * C57BL/6J	N	22161748
MGI:5435559	F	MP:0002759	abnormal caudal vertebrae morphology	Porcn<tm1Vdv>/Porcn<+>	chimera involves: 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435559	F	MP:0000565	oligodactyly	Porcn<tm1Vdv>/Porcn<+>	chimera involves: 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435559	F	MP:0002544	brachydactyly	Porcn<tm1Vdv>/Porcn<+>	chimera involves: 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435559	F	MP:0008730	fused phalanges	Porcn<tm1Vdv>/Porcn<+>	chimera involves: 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435559	F	MP:0000519	hydronephrosis	Porcn<tm1Vdv>/Porcn<+>	chimera involves: 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435559	F	MP:0009085	abnormal uterine horn morphology	Porcn<tm1Vdv>/Porcn<+>	chimera involves: 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435560	M	MP:0002759	abnormal caudal vertebrae morphology	Porcn<tm1Vdv>/Y	chimera involves: 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435560	M	MP:0000565	oligodactyly	Porcn<tm1Vdv>/Y	chimera involves: 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435560	M	MP:0000519	hydronephrosis	Porcn<tm1Vdv>/Y	chimera involves: 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435560	M	MP:0001147	small testis	Porcn<tm1Vdv>/Y	chimera involves: 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435560	M	MP:0002544	brachydactyly	Porcn<tm1Vdv>/Y	chimera involves: 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435560	M	MP:0008730	fused phalanges	Porcn<tm1Vdv>/Y	chimera involves: 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435561	F	MP:0002073	abnormal hair growth	Porcn<tm1.1Vdv>/Porcn<+>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	N	22412863
MGI:5435561	F	MP:0011101	prenatal lethality, incomplete penetrance	Porcn<tm1.1Vdv>/Porcn<+>,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	N	22412863
MGI:5435562	M	MP:0011101	prenatal lethality, incomplete penetrance	Porcn<tm1.1Vdv>/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	N	22412863
MGI:5435562	M	MP:0002073	abnormal hair growth	Porcn<tm1.1Vdv>/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	N	22412863
MGI:5435563	F	MP:0002073	abnormal hair growth	Porcn<tm1.2Vdv>/Porcn<+>	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	N	22412863
MGI:5435563	F	MP:0011101	prenatal lethality, incomplete penetrance	Porcn<tm1.2Vdv>/Porcn<+>	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	N	22412863
MGI:5435563	F	MP:0011102	embryonic lethality, incomplete penetrance	Porcn<tm1.2Vdv>/Porcn<+>	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	N	22412863
MGI:5435564	M	MP:0011092	embryonic lethality, complete penetrance	Porcn<tm1.2Vdv>/Y	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	N	22412863
MGI:5435565	F	MP:0003384	abnormal ventral body wall morphology	Porcn<tm1.1Vdv>/Porcn<+>,Hprt1<tm1(CAG-cre)Mnn>/Hprt1<+>	involves: 129S/Sv * C57BL/6J	N	22412863
MGI:5435565	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Porcn<tm1.1Vdv>/Porcn<+>,Hprt1<tm1(CAG-cre)Mnn>/Hprt1<+>	involves: 129S/Sv * C57BL/6J	N	22412863
MGI:5435565	F	MP:0004073	caudal body truncation	Porcn<tm1.1Vdv>/Porcn<+>,Hprt1<tm1(CAG-cre)Mnn>/Hprt1<+>	involves: 129S/Sv * C57BL/6J	N	22412863
MGI:5435565	F	MP:0000929	open neural tube	Porcn<tm1.1Vdv>/Porcn<+>,Hprt1<tm1(CAG-cre)Mnn>/Hprt1<+>	involves: 129S/Sv * C57BL/6J	N	22412863
MGI:5435565	F	MP:0011091	prenatal lethality, complete penetrance	Porcn<tm1.1Vdv>/Porcn<+>,Hprt1<tm1(CAG-cre)Mnn>/Hprt1<+>	involves: 129S/Sv * C57BL/6J	N	22412863
MGI:5435565	F	MP:0003984	embryonic growth retardation	Porcn<tm1.1Vdv>/Porcn<+>,Hprt1<tm1(CAG-cre)Mnn>/Hprt1<+>	involves: 129S/Sv * C57BL/6J	N	22412863
MGI:5435567	M	MP:0001265	decreased body size	Porcn<tm1.1Vdv>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6 * SJL/J	N	22412863
MGI:5435567	M	MP:0000564	syndactyly	Porcn<tm1.1Vdv>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6 * SJL/J	N	22412863
MGI:5435567	M	MP:0002544	brachydactyly	Porcn<tm1.1Vdv>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6 * SJL/J	N	22412863
MGI:5435567	M	MP:0000547	short limbs	Porcn<tm1.1Vdv>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6 * SJL/J	N	22412863
MGI:5435567	M	MP:0001732	postnatal growth retardation	Porcn<tm1.1Vdv>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6 * SJL/J	N	22412863
MGI:5435567	M	MP:0004686	decreased length of long bones	Porcn<tm1.1Vdv>/Y,Tg(Prrx1-cre)1Cjt/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6 * SJL/J	N	22412863
MGI:5435568	M	MP:0003704	abnormal hair follicle development	Porcn<tm1.1Vdv>/Y,Tg(KRT14-cre)1Efu/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435568	M	MP:0002100	abnormal tooth morphology	Porcn<tm1.1Vdv>/Y,Tg(KRT14-cre)1Efu/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435568	M	MP:0001199	thin skin	Porcn<tm1.1Vdv>/Y,Tg(KRT14-cre)1Efu/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435568	M	MP:0000414	alopecia	Porcn<tm1.1Vdv>/Y,Tg(KRT14-cre)1Efu/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435568	M	MP:0011156	abnormal hypodermis fat layer morphology	Porcn<tm1.1Vdv>/Y,Tg(KRT14-cre)1Efu/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435569	F	MP:0002073	abnormal hair growth	Porcn<tm1.1Vdv>/Porcn<+>,Tg(KRT14-cre)1Efu/0	involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J	N	22412863
MGI:5435702	F	MP:0001441	increased grooming behavior	Shank2<tm1.1Tmb>/Shank2<tm1.1Tmb>	B6.129-Shank2<tm1.1Tmb>	N	22699619
MGI:5435702	F	MP:0001529	abnormal vocalization	Shank2<tm1.1Tmb>/Shank2<tm1.1Tmb>	B6.129-Shank2<tm1.1Tmb>	N	22699619
MGI:5435702	M	MP:0002566	abnormal sexual interaction	Shank2<tm1.1Tmb>/Shank2<tm1.1Tmb>	B6.129-Shank2<tm1.1Tmb>	N	22699619
MGI:5435702	M	MP:0002863	improved righting response	Shank2<tm1.1Tmb>/Shank2<tm1.1Tmb>	B6.129-Shank2<tm1.1Tmb>	N	22699619
MGI:5435702	F	MP:0001523	impaired righting response	Shank2<tm1.1Tmb>/Shank2<tm1.1Tmb>	B6.129-Shank2<tm1.1Tmb>	N	22699619
MGI:5436309	M	MP:0001406	abnormal gait	Pink1<tm1.1Wrst>/Pink1<tm1.1Wrst>	involves: 129S2/SvPas * BALB/cJ * C57BL/6J	N	22265660
MGI:5436309	M	MP:0001984	abnormal olfaction	Pink1<tm1.1Wrst>/Pink1<tm1.1Wrst>	involves: 129S2/SvPas * BALB/cJ * C57BL/6J	N	22265660
MGI:5436422	M	MP:0002687	oligozoospermia	Cip2a<Gt(CD0252)Wtsi>/Cip2a<Gt(CD0252)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	22461891
MGI:5436422	M	MP:0004930	small epididymis	Cip2a<Gt(CD0252)Wtsi>/Cip2a<Gt(CD0252)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	22461891
MGI:5436422	M	MP:0001156	abnormal spermatogenesis	Cip2a<Gt(CD0252)Wtsi>/Cip2a<Gt(CD0252)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	22461891
MGI:5436422	M	MP:0004929	decreased epididymis weight	Cip2a<Gt(CD0252)Wtsi>/Cip2a<Gt(CD0252)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	22461891
MGI:5437301	F	MP:0009671	abnormal uterus physiology	Antxr2<tm1.1Jkit>/Antxr2<tm1.1Jkit>	involves: 129 * C57BL/6	N	22529944
MGI:5437301	F	MP:0008256	abnormal myometrium morphology	Antxr2<tm1.1Jkit>/Antxr2<tm1.1Jkit>	involves: 129 * C57BL/6	N	22529944
MGI:5437301	F	MP:0005389	reproductive system phenotype	Antxr2<tm1.1Jkit>/Antxr2<tm1.1Jkit>	involves: 129 * C57BL/6	Y	22529944
MGI:5437301	F	MP:0004038	lymphangiectasis	Antxr2<tm1.1Jkit>/Antxr2<tm1.1Jkit>	involves: 129 * C57BL/6	N	22529944
MGI:5437301	F	MP:0031434	increased miscarriage rate	Antxr2<tm1.1Jkit>/Antxr2<tm1.1Jkit>	involves: 129 * C57BL/6	N	22529944
MGI:5437301	F	MP:0006042	increased apoptosis	Antxr2<tm1.1Jkit>/Antxr2<tm1.1Jkit>	involves: 129 * C57BL/6	N	22529944
MGI:5437301	F	MP:0012010	parturition failure	Antxr2<tm1.1Jkit>/Antxr2<tm1.1Jkit>	involves: 129 * C57BL/6	N	22529944
MGI:5437301	F	MP:0009209	abnormal internal female genitalia morphology	Antxr2<tm1.1Jkit>/Antxr2<tm1.1Jkit>	involves: 129 * C57BL/6	N	22529944
MGI:5437301	F	MP:0001120	abnormal uterus morphology	Antxr2<tm1.1Jkit>/Antxr2<tm1.1Jkit>	involves: 129 * C57BL/6	N	22529944
MGI:5437301	F	MP:0008028	pregnancy-related premature death	Antxr2<tm1.1Jkit>/Antxr2<tm1.1Jkit>	involves: 129 * C57BL/6	N	22529944
MGI:5437301	F	MP:0004938	dilated vasculature	Antxr2<tm1.1Jkit>/Antxr2<tm1.1Jkit>	involves: 129 * C57BL/6	N	22529944
MGI:5437301	F	MP:0001926	female infertility	Antxr2<tm1.1Jkit>/Antxr2<tm1.1Jkit>	involves: 129 * C57BL/6	N	22529944
MGI:5437301	F	MP:0001135	abnormal uterine cervix morphology	Antxr2<tm1.1Jkit>/Antxr2<tm1.1Jkit>	involves: 129 * C57BL/6	N	22529944
MGI:5437367	M	MP:0001922	reduced male fertility	Chd7<Ome>/Chd7<+>	involves: BALB/cByJ * C57BL/6J	N	22539951
MGI:5437480	M	MP:0001405	impaired coordination	Shank2<tm1Mgle>/Shank2<tm1Mgle>	B6.129S4-Shank2<tm1Mgle>	N	27903723
MGI:5437480	M	MP:0001447	abnormal nest building behavior	Shank2<tm1Mgle>/Shank2<tm1Mgle>	B6.129S4-Shank2<tm1Mgle>	N	22699620
MGI:5437480	M	MP:0001441	increased grooming behavior	Shank2<tm1Mgle>/Shank2<tm1Mgle>	B6.129S4-Shank2<tm1Mgle>	N	22699620
MGI:5437480	M	MP:0001363	increased anxiety-related response	Shank2<tm1Mgle>/Shank2<tm1Mgle>	B6.129S4-Shank2<tm1Mgle>	N	27903723
MGI:5437480	M	MP:0020351	decreased vocalization	Shank2<tm1Mgle>/Shank2<tm1Mgle>	B6.129S4-Shank2<tm1Mgle>	N	22699620
MGI:5437480	F	MP:0001384	abnormal pup retrieval	Shank2<tm1Mgle>/Shank2<tm1Mgle>	B6.129S4-Shank2<tm1Mgle>	N	22699620
MGI:5437482	M	MP:0000496	abnormal small intestine morphology	Yipf6<M1Btlr>/Y	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437482	M	MP:0000495	abnormal colon morphology	Yipf6<M1Btlr>/Y	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437482	M	MP:0010180	increased susceptibility to weight loss	Yipf6<M1Btlr>/Y	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437482	M	MP:0002816	colitis	Yipf6<M1Btlr>/Y	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437482	M	MP:0004843	abnormal Paneth cell morphology	Yipf6<M1Btlr>/Y	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437482	M	MP:0009146	abnormal pancreatic acinar cell morphology	Yipf6<M1Btlr>/Y	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437482	M	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality	Yipf6<M1Btlr>/Y	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437482	M	MP:0008537	increased susceptibility to induced colitis	Yipf6<M1Btlr>/Y	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437482	M	MP:0003449	abnormal intestinal goblet cell morphology	Yipf6<M1Btlr>/Y	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437482	M	MP:0013486	decreased Paneth cell number	Yipf6<M1Btlr>/Y	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437483	F	MP:0004843	abnormal Paneth cell morphology	Yipf6<M1Btlr>/Yipf6<M1Btlr>	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437483	F	MP:0000495	abnormal colon morphology	Yipf6<M1Btlr>/Yipf6<M1Btlr>	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437483	F	MP:0010180	increased susceptibility to weight loss	Yipf6<M1Btlr>/Yipf6<M1Btlr>	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437483	F	MP:0008537	increased susceptibility to induced colitis	Yipf6<M1Btlr>/Yipf6<M1Btlr>	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437483	F	MP:0002816	colitis	Yipf6<M1Btlr>/Yipf6<M1Btlr>	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437483	F	MP:0000496	abnormal small intestine morphology	Yipf6<M1Btlr>/Yipf6<M1Btlr>	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437483	F	MP:0003449	abnormal intestinal goblet cell morphology	Yipf6<M1Btlr>/Yipf6<M1Btlr>	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437483	F	MP:0013486	decreased Paneth cell number	Yipf6<M1Btlr>/Yipf6<M1Btlr>	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437483	F	MP:0009146	abnormal pancreatic acinar cell morphology	Yipf6<M1Btlr>/Yipf6<M1Btlr>	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437483	F	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality	Yipf6<M1Btlr>/Yipf6<M1Btlr>	C57BL/6J-Yipf6<M1Btlr>/Mmucd	N	22802641
MGI:5437710	M	MP:0010144	abnormal tumor vascularization	X/Tg(SERPINC1-SV40)BPbr	involves: C57BL/6 * DBA/2	N	12763373
MGI:5437710	M	MP:0005425	increased macrophage cell number	X/Tg(SERPINC1-SV40)BPbr	involves: C57BL/6 * DBA/2	N	12763373
MGI:5437710	M	MP:0003331	increased hepatocellular carcinoma incidence	X/Tg(SERPINC1-SV40)BPbr	involves: C57BL/6 * DBA/2	N	1660504
MGI:5437710	M	MP:0003331	increased hepatocellular carcinoma incidence	X/Tg(SERPINC1-SV40)BPbr	involves: C57BL/6 * DBA/2	N	12763373
MGI:5437710	M	MP:0003324	increased liver adenoma incidence	X/Tg(SERPINC1-SV40)BPbr	involves: C57BL/6 * DBA/2	N	12763373
MGI:5437747	M	MP:0004042	decreased susceptibility to kidney reperfusion injury	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Hprt1<tm1(Pck1-cre)Vhh>/Y	involves: 129 * 129P2/OlaHsd	N	20360310
MGI:5437747	M	MP:0005367	renal/urinary system phenotype	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Hprt1<tm1(Pck1-cre)Vhh>/Y	involves: 129 * 129P2/OlaHsd	Y	20360310
MGI:5437751	F	MP:0001125	abnormal oocyte morphology	Pabpc1l<tm1.1Esel>/Pabpc1l<tm1.1Esel>	involves: 129S1/SvImJ * C57BL/6J	N	22621333
MGI:5437751	F	MP:0009433	polyovular ovarian follicle	Pabpc1l<tm1.1Esel>/Pabpc1l<tm1.1Esel>	involves: 129S1/SvImJ * C57BL/6J	N	22621333
MGI:5437751	F	MP:0000242	impaired fertilization	Pabpc1l<tm1.1Esel>/Pabpc1l<tm1.1Esel>	involves: 129S1/SvImJ * C57BL/6J	N	22621333
MGI:5437751	F	MP:0031383	increased secondary ovarian follicle number	Pabpc1l<tm1.1Esel>/Pabpc1l<tm1.1Esel>	involves: 129S1/SvImJ * C57BL/6J	N	22621333
MGI:5437751	F	MP:0001131	abnormal ovarian follicle morphology	Pabpc1l<tm1.1Esel>/Pabpc1l<tm1.1Esel>	involves: 129S1/SvImJ * C57BL/6J	N	22621333
MGI:5437751	F	MP:0001926	female infertility	Pabpc1l<tm1.1Esel>/Pabpc1l<tm1.1Esel>	involves: 129S1/SvImJ * C57BL/6J	N	22621333
MGI:5437751	F	MP:0011701	decreased cumulus expansion	Pabpc1l<tm1.1Esel>/Pabpc1l<tm1.1Esel>	involves: 129S1/SvImJ * C57BL/6J	N	22621333
MGI:5437751	F	MP:0001931	abnormal oogenesis	Pabpc1l<tm1.1Esel>/Pabpc1l<tm1.1Esel>	involves: 129S1/SvImJ * C57BL/6J	N	22621333
MGI:5437751	F	MP:0005621	abnormal cell physiology	Pabpc1l<tm1.1Esel>/Pabpc1l<tm1.1Esel>	involves: 129S1/SvImJ * C57BL/6J	N	22621333
MGI:5437751	F	MP:0003355	decreased ovulation rate	Pabpc1l<tm1.1Esel>/Pabpc1l<tm1.1Esel>	involves: 129S1/SvImJ * C57BL/6J	N	22621333
MGI:5437751	F	MP:0014445	abnormal spindle assembly in female meiosis	Pabpc1l<tm1.1Esel>/Pabpc1l<tm1.1Esel>	involves: 129S1/SvImJ * C57BL/6J	N	22621333
MGI:5437751	F	MP:0005431	decreased oocyte number	Pabpc1l<tm1.1Esel>/Pabpc1l<tm1.1Esel>	involves: 129S1/SvImJ * C57BL/6J	N	22621333
MGI:5437999	M	MP:0009289	decreased epididymal fat pad weight	Tg(Myl2-FGF19)1Dfre/?	involves: FVB	N	11956156
MGI:5438016	M	MP:0005369	muscle phenotype	Hprt1<tm2(CAG-Myof)Isrd>/Y	involves: 129 * C57BL/6	Y	22666441
MGI:5438017	F	MP:0005369	muscle phenotype	Hprt1<tm2(CAG-Myof)Isrd>/Hprt1<tm2(CAG-Myof)Isrd>	involves: 129 * C57BL/6	Y	22666441
MGI:5438018	M	MP:0005376	homeostasis/metabolism phenotype	Dysf<prmd>/Dysf<prmd>,Hprt1<tm2(CAG-Myof)Isrd>/Y	involves: 129 * A/J * C57BL/6	Y	22666441
MGI:5438018	M	MP:0000752	dystrophic muscle	Dysf<prmd>/Dysf<prmd>,Hprt1<tm2(CAG-Myof)Isrd>/Y	involves: 129 * A/J * C57BL/6	N	22666441
MGI:5438018	M	MP:0005369	muscle phenotype	Dysf<prmd>/Dysf<prmd>,Hprt1<tm2(CAG-Myof)Isrd>/Y	involves: 129 * A/J * C57BL/6	Y	22666441
MGI:5438019	F	MP:0000752	dystrophic muscle	Dysf<prmd>/Dysf<prmd>,Hprt1<tm2(CAG-Myof)Isrd>/Hprt1<tm2(CAG-Myof)Isrd>	involves: 129 * A/J * C57BL/6	N	22666441
MGI:5438019	F	MP:0005369	muscle phenotype	Dysf<prmd>/Dysf<prmd>,Hprt1<tm2(CAG-Myof)Isrd>/Hprt1<tm2(CAG-Myof)Isrd>	involves: 129 * A/J * C57BL/6	Y	22666441
MGI:5438019	F	MP:0005376	homeostasis/metabolism phenotype	Dysf<prmd>/Dysf<prmd>,Hprt1<tm2(CAG-Myof)Isrd>/Hprt1<tm2(CAG-Myof)Isrd>	involves: 129 * A/J * C57BL/6	Y	22666441
MGI:5438090	M	MP:0002051	increased skin papilloma incidence	Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)6Tuv/0,Usp9x<tm1Tuv>/Y	involves: 129S4/SvJae * FVB/N	N	22699621
MGI:5438090	M	MP:0009153	increased pancreas tumor incidence	Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)6Tuv/0,Usp9x<tm1Tuv>/Y	involves: 129S4/SvJae * FVB/N	N	22699621
MGI:5438090	M	MP:0009152	increased pancreatic intraepithelial neoplasia incidence	Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)6Tuv/0,Usp9x<tm1Tuv>/Y	involves: 129S4/SvJae * FVB/N	N	22699621
MGI:5438090	M	MP:0003752	increased oral papilloma incidence	Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)6Tuv/0,Usp9x<tm1Tuv>/Y	involves: 129S4/SvJae * FVB/N	N	22699621
MGI:5438090	M	MP:0002083	premature death	Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)6Tuv/0,Usp9x<tm1Tuv>/Y	involves: 129S4/SvJae * FVB/N	N	22699621
MGI:5438091	F	MP:0002083	premature death	Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)6Tuv/0,Usp9x<tm1Tuv>/Usp9x<+>	involves: 129S4/SvJae * FVB/N	N	22699621
MGI:5438091	F	MP:0003752	increased oral papilloma incidence	Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)6Tuv/0,Usp9x<tm1Tuv>/Usp9x<+>	involves: 129S4/SvJae * FVB/N	N	22699621
MGI:5438091	F	MP:0002051	increased skin papilloma incidence	Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)6Tuv/0,Usp9x<tm1Tuv>/Usp9x<+>	involves: 129S4/SvJae * FVB/N	N	22699621
MGI:5438091	F	MP:0009152	increased pancreatic intraepithelial neoplasia incidence	Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)6Tuv/0,Usp9x<tm1Tuv>/Usp9x<+>	involves: 129S4/SvJae * FVB/N	N	22699621
MGI:5438091	F	MP:0009153	increased pancreas tumor incidence	Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)6Tuv/0,Usp9x<tm1Tuv>/Usp9x<+>	involves: 129S4/SvJae * FVB/N	N	22699621
MGI:5438105	F	MP:0005292	improved glucose tolerance	Cox4i2<tm1Hutt>/Cox4i2<tm1Hutt>	B6.129-Cox4i2<tm1Hutt>	N	22730437
MGI:5438105	F	MP:0010053	decreased grip strength	Cox4i2<tm1Hutt>/Cox4i2<tm1Hutt>	B6.129-Cox4i2<tm1Hutt>	N	22730437
MGI:5438221	F	MP:0004762	increased anti-double stranded DNA antibody level	Mfge8<tm1Osa>/Mfge8<tm1Osa>,Timd4<tm1Osa>/Timd4<tm1Osa>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22723547
MGI:5438221	F	MP:0004794	increased anti-nuclear antigen antibody level	Mfge8<tm1Osa>/Mfge8<tm1Osa>,Timd4<tm1Osa>/Timd4<tm1Osa>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22723547
MGI:5438241	M	MP:0009936	abnormal dendritic spine morphology	Cul4b<tm1Swl>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	B6.Cg-Edil3<Tg(Sox2-cre)1Amc> Cul4b<tm1Swl>	N	22763239
MGI:5438241	M	MP:0008143	abnormal dendrite morphology	Cul4b<tm1Swl>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	B6.Cg-Edil3<Tg(Sox2-cre)1Amc> Cul4b<tm1Swl>	N	22763239
MGI:5438241	M	MP:0008948	decreased neuron number	Cul4b<tm1Swl>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	B6.Cg-Edil3<Tg(Sox2-cre)1Amc> Cul4b<tm1Swl>	N	22763239
MGI:5438241	M	MP:0002906	increased susceptibility to pharmacologically induced seizures	Cul4b<tm1Swl>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	B6.Cg-Edil3<Tg(Sox2-cre)1Amc> Cul4b<tm1Swl>	N	22763239
MGI:5438241	M	MP:0001463	abnormal spatial learning	Cul4b<tm1Swl>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	B6.Cg-Edil3<Tg(Sox2-cre)1Amc> Cul4b<tm1Swl>	N	22763239
MGI:5438241	M	MP:0014370	impaired spatial working memory	Cul4b<tm1Swl>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	B6.Cg-Edil3<Tg(Sox2-cre)1Amc> Cul4b<tm1Swl>	N	22763239
MGI:5438289	M	MP:0005169	abnormal male meiosis	Rnf212<tm1Nhtr>/Rnf212<tm1Nhtr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22761591
MGI:5438290	M	MP:0005169	abnormal male meiosis	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6J	N	22761591
MGI:5438302	M	MP:0008261	arrest of male meiosis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J	N	24589552
MGI:5438302	M	MP:0005169	abnormal male meiosis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J	N	22761591
MGI:5438302	M	MP:0009451	abnormal chromosomal synapsis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J	N	24589552
MGI:5438302	M	MP:0005169	abnormal male meiosis	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J	N	24589552
MGI:5438302	M	MP:0010948	abnormal double-strand DNA break repair	Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J	N	24589552
MGI:5438321	M	MP:0002686	globozoospermia	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0002216	abnormal seminiferous tubule morphology	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0009836	abnormal sperm principal piece morphology	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0004543	abnormal sperm physiology	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0009377	ectopic manchette	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0009376	abnormal manchette morphology	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0008898	abnormal acrosome morphology	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0001147	small testis	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0009833	absent sperm mitochondrial sheath	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0006362	abnormal male germ cell morphology	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0031372	abnormal sperm individualization	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0031386	elongated manchette	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0004852	decreased testis weight	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0009831	abnormal sperm midpiece morphology	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0009231	detached acrosome	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0001925	male infertility	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0009238	coiled sperm flagellum	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438321	M	MP:0009839	multiflagellated sperm	Dpy19l2<tm1Lex>/Dpy19l2<tm1Lex>	B6;129S5-Dpy19l2<tm1Lex>/Mmucd	N	22764053
MGI:5438332	F	MP:0003675	kidney cyst	Pkhd1<tm2Cjwa>/Pkhd1<tm2Cjwa>	either: B6.129(Cg)-Pkhd1<tm2Cjwa> or C.129(Cg)-Pkhd1<tm2Cjwa>	N	22021705
MGI:5438332	F	MP:0009050	dilated proximal convoluted tubule	Pkhd1<tm2Cjwa>/Pkhd1<tm2Cjwa>	either: B6.129(Cg)-Pkhd1<tm2Cjwa> or C.129(Cg)-Pkhd1<tm2Cjwa>	N	22021705
MGI:5438527	M	MP:0004852	decreased testis weight	Ago4<tm1.1Peco>/Ago4<tm1.1Peco>	B6.129P2(FVB)-Ago4<tm1.1Peco>	N	22863743
MGI:5438527	M	MP:0002687	oligozoospermia	Ago4<tm1.1Peco>/Ago4<tm1.1Peco>	B6.129P2(FVB)-Ago4<tm1.1Peco>	N	22863743
MGI:5438527	M	MP:0009452	abnormal synaptonemal complex	Ago4<tm1.1Peco>/Ago4<tm1.1Peco>	B6.129P2(FVB)-Ago4<tm1.1Peco>	N	22863743
MGI:5438527	M	MP:0014052	increased male germ cell apoptosis	Ago4<tm1.1Peco>/Ago4<tm1.1Peco>	B6.129P2(FVB)-Ago4<tm1.1Peco>	N	22863743
MGI:5438527	M	MP:0005169	abnormal male meiosis	Ago4<tm1.1Peco>/Ago4<tm1.1Peco>	B6.129P2(FVB)-Ago4<tm1.1Peco>	N	22863743
MGI:5438527	M	MP:0006362	abnormal male germ cell morphology	Ago4<tm1.1Peco>/Ago4<tm1.1Peco>	B6.129P2(FVB)-Ago4<tm1.1Peco>	N	22863743
MGI:5438566	M	MP:0005389	reproductive system phenotype	Tmeff2<tm1Fawa>/Tmeff2<tm1Fawa>	involves: 129P2/OlaHsd	Y	22828515
MGI:5438598	M	MP:0001552	increased circulating triglyceride level	Nos3<tm1.2Taka>/Nos3<tm1.2Taka>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J * CBA	N	22467476
MGI:5438598	F	MP:0005559	increased circulating glucose level	Nos3<tm1.2Taka>/Nos3<tm1.2Taka>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J * CBA	N	22467476
MGI:5438706	M	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Kdm6a<tm1a(EUCOMM)Jhha>/Y,Tg(Pgk1-cre)1Lni/0	involves: 129 * BALB/c * C57BL/6 * DBA	N	22801502
MGI:5438706	M	MP:0003984	embryonic growth retardation	Kdm6a<tm1a(EUCOMM)Jhha>/Y,Tg(Pgk1-cre)1Lni/0	involves: 129 * BALB/c * C57BL/6 * DBA	N	22801502
MGI:5438707	F	MP:0000929	open neural tube	Kdm6a<tm1a(EUCOMM)Jhha>/Kdm6a<tm1b(EUCOMM)Jhha>,Tg(Pgk1-cre)1Lni/0	involves: 129 * BALB/c * C57BL/6 * DBA	N	22801502
MGI:5438707	F	MP:0006207	embryonic lethality during organogenesis	Kdm6a<tm1a(EUCOMM)Jhha>/Kdm6a<tm1b(EUCOMM)Jhha>,Tg(Pgk1-cre)1Lni/0	involves: 129 * BALB/c * C57BL/6 * DBA	N	22801502
MGI:5438997	F	MP:0010090	increased circulating creatine kinase level	Dag1<tm1.1Swin>/Dag1<tm1.1Swin>,Dmd<mdx>/Dmd<mdx>	involves: 129S4/SvJae * C57BL/6 * C57BL/10ScSn	N	22810924
MGI:5438997	F	MP:0005165	increased susceptibility to injury	Dag1<tm1.1Swin>/Dag1<tm1.1Swin>,Dmd<mdx>/Dmd<mdx>	involves: 129S4/SvJae * C57BL/6 * C57BL/10ScSn	N	22810924
MGI:5438997	F	MP:0009404	centrally nucleated skeletal muscle fibers	Dag1<tm1.1Swin>/Dag1<tm1.1Swin>,Dmd<mdx>/Dmd<mdx>	involves: 129S4/SvJae * C57BL/6 * C57BL/10ScSn	N	22810924
MGI:5438998	M	MP:0005165	increased susceptibility to injury	Dag1<tm1.1Swin>/Dag1<tm1.1Swin>,Dmd<mdx>/Y	involves: 129S4/SvJae * C57BL/6 * C57BL/10ScSn	N	22810924
MGI:5438998	M	MP:0009404	centrally nucleated skeletal muscle fibers	Dag1<tm1.1Swin>/Dag1<tm1.1Swin>,Dmd<mdx>/Y	involves: 129S4/SvJae * C57BL/6 * C57BL/10ScSn	N	22810924
MGI:5438998	M	MP:0010090	increased circulating creatine kinase level	Dag1<tm1.1Swin>/Dag1<tm1.1Swin>,Dmd<mdx>/Y	involves: 129S4/SvJae * C57BL/6 * C57BL/10ScSn	N	22810924
MGI:5439018	M	MP:0004728	abnormal efferent ductules of testis morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Defb41<tm1(icre)Psip>/Defb41<+>	involves: 129S6/SvEvTac * C57BL/6N	N	22701646
MGI:5439018	M	MP:0004930	small epididymis	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Defb41<tm1(icre)Psip>/Defb41<+>	involves: 129S6/SvEvTac * C57BL/6N	N	22701646
MGI:5439018	M	MP:0009140	dilated efferent ductule of testis	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Defb41<tm1(icre)Psip>/Defb41<+>	involves: 129S6/SvEvTac * C57BL/6N	N	22701646
MGI:5439018	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Defb41<tm1(icre)Psip>/Defb41<+>	involves: 129S6/SvEvTac * C57BL/6N	N	22701646
MGI:5439018	M	MP:0014194	increased epididymal epithelium cell proliferation	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Defb41<tm1(icre)Psip>/Defb41<+>	involves: 129S6/SvEvTac * C57BL/6N	N	22701646
MGI:5439018	M	MP:0004933	abnormal epididymis epithelium morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Defb41<tm1(icre)Psip>/Defb41<+>	involves: 129S6/SvEvTac * C57BL/6N	N	22701646
MGI:5439018	M	MP:0002631	abnormal epididymis morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Defb41<tm1(icre)Psip>/Defb41<+>	involves: 129S6/SvEvTac * C57BL/6N	N	22701646
MGI:5439018	M	MP:0002687	oligozoospermia	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Defb41<tm1(icre)Psip>/Defb41<+>	involves: 129S6/SvEvTac * C57BL/6N	N	22701646
MGI:5439018	M	MP:0001925	male infertility	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Defb41<tm1(icre)Psip>/Defb41<+>	involves: 129S6/SvEvTac * C57BL/6N	N	22701646
MGI:5439173	M	MP:0001406	abnormal gait	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439173	M	MP:0000748	progressive muscle weakness	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439173	M	MP:0009420	skeletal muscle endomysial fibrosis	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439173	M	MP:0004232	decreased muscle weight	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439173	M	MP:0011086	postnatal lethality, incomplete penetrance	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439173	M	MP:0002279	abnormal diaphragm morphology	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439173	M	MP:0009403	increased variability of skeletal muscle fiber size	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439173	M	MP:0001265	decreased body size	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439173	M	MP:0000160	kyphosis	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439173	M	MP:0001402	decreased locomotor activity	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439173	M	MP:0013239	impaired skeletal muscle regeneration	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439173	M	MP:0009414	skeletal muscle fiber necrosis	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439173	M	MP:0000761	thin diaphragm muscle	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439173	M	MP:0009419	skeletal muscle fibrosis	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Y	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0009419	skeletal muscle fibrosis	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0002279	abnormal diaphragm morphology	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0001265	decreased body size	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0000160	kyphosis	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0000761	thin diaphragm muscle	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0013239	impaired skeletal muscle regeneration	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0001406	abnormal gait	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0009414	skeletal muscle fiber necrosis	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0001402	decreased locomotor activity	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0004232	decreased muscle weight	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0009403	increased variability of skeletal muscle fiber size	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0009420	skeletal muscle endomysial fibrosis	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0000748	progressive muscle weakness	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439179	F	MP:0011086	postnatal lethality, incomplete penetrance	Barx2<tm1Rsd>/Barx2<tm1Rsd>,Dmd<mdx>/Dmd<mdx>	involves: 129 * C57BL/6 * C57BL/10ScSn	N	22076929
MGI:5439283	M	MP:0002686	globozoospermia	Spaca1<tm1.1Osb>/Spaca1<tm1.1Osb>	involves: 129S2/SvPas * C57BL * C57BL/6N * DBA	N	22949614
MGI:5439283	M	MP:0008898	abnormal acrosome morphology	Spaca1<tm1.1Osb>/Spaca1<tm1.1Osb>	involves: 129S2/SvPas * C57BL * C57BL/6N * DBA	N	22949614
MGI:5439283	M	MP:0001925	male infertility	Spaca1<tm1.1Osb>/Spaca1<tm1.1Osb>	involves: 129S2/SvPas * C57BL * C57BL/6N * DBA	N	22949614
MGI:5439283	M	MP:0002675	asthenozoospermia	Spaca1<tm1.1Osb>/Spaca1<tm1.1Osb>	involves: 129S2/SvPas * C57BL * C57BL/6N * DBA	N	22949614
MGI:5439283	M	MP:0005578	teratozoospermia	Spaca1<tm1.1Osb>/Spaca1<tm1.1Osb>	involves: 129S2/SvPas * C57BL * C57BL/6N * DBA	N	22949614
MGI:5439283	M	MP:0008892	abnormal sperm flagellum morphology	Spaca1<tm1.1Osb>/Spaca1<tm1.1Osb>	involves: 129S2/SvPas * C57BL * C57BL/6N * DBA	N	22949614
MGI:5439283	M	MP:0009238	coiled sperm flagellum	Spaca1<tm1.1Osb>/Spaca1<tm1.1Osb>	involves: 129S2/SvPas * C57BL * C57BL/6N * DBA	N	22949614
MGI:5439283	M	MP:0009230	abnormal sperm head morphology	Spaca1<tm1.1Osb>/Spaca1<tm1.1Osb>	involves: 129S2/SvPas * C57BL * C57BL/6N * DBA	N	22949614
MGI:5439284	M	MP:0008898	abnormal acrosome morphology	Spaca1<tm1.1Osb>/Spaca1<tm1.1Osb>,Tg(Acr-EGFP)1Osb/0	involves: 129S2/SvPas * C3H * C57BL * C57BL/6 * DBA	N	22949614
MGI:5439284	M	MP:0006380	abnormal spermatid morphology	Spaca1<tm1.1Osb>/Spaca1<tm1.1Osb>,Tg(Acr-EGFP)1Osb/0	involves: 129S2/SvPas * C3H * C57BL * C57BL/6 * DBA	N	22949614
MGI:5439284	M	MP:0002686	globozoospermia	Spaca1<tm1.1Osb>/Spaca1<tm1.1Osb>,Tg(Acr-EGFP)1Osb/0	involves: 129S2/SvPas * C3H * C57BL * C57BL/6 * DBA	N	22949614
MGI:5439284	M	MP:0001156	abnormal spermatogenesis	Spaca1<tm1.1Osb>/Spaca1<tm1.1Osb>,Tg(Acr-EGFP)1Osb/0	involves: 129S2/SvPas * C3H * C57BL * C57BL/6 * DBA	N	22949614
MGI:5439487	M	MP:0005367	renal/urinary system phenotype	Ptger2<tm2Bhk>/Ptger2<tm2Bhk>	involves: 129P2/OlaHsd	Y	11123248
MGI:5439487	M	MP:0005385	cardiovascular system phenotype	Ptger2<tm2Bhk>/Ptger2<tm2Bhk>	involves: 129P2/OlaHsd	Y	11123248
MGI:5439488	M	MP:0005530	decreased renal vascular resistance	Ptger3<tm1Cof>/Ptger3<tm1Cof>	involves: 129P2/OlaHsd	N	11123248
MGI:5439488	M	MP:0005590	increased vasodilation	Ptger3<tm1Cof>/Ptger3<tm1Cof>	involves: 129P2/OlaHsd	N	11123248
MGI:5439488	M	MP:0005385	cardiovascular system phenotype	Ptger3<tm1Cof>/Ptger3<tm1Cof>	involves: 129P2/OlaHsd	Y	11123248
MGI:5439488	M	MP:0005525	increased renal plasma flow rate	Ptger3<tm1Cof>/Ptger3<tm1Cof>	involves: 129P2/OlaHsd	N	11123248
MGI:5439488	M	MP:0005367	renal/urinary system phenotype	Ptger3<tm1Cof>/Ptger3<tm1Cof>	involves: 129P2/OlaHsd	Y	11123248
MGI:5439494	M	MP:0001876	decreased inflammatory response	Mep1b<tm1Bond>/Mep1b<tm1Bond>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18172000
MGI:5439494	M	MP:0005554	decreased circulating creatinine level	Mep1b<tm1Bond>/Mep1b<tm1Bond>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18172000
MGI:5439494	M	MP:0011352	proximal convoluted tubule brush border loss	Mep1b<tm1Bond>/Mep1b<tm1Bond>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18172000
MGI:5439494	M	MP:0009643	abnormal urine homeostasis	Mep1b<tm1Bond>/Mep1b<tm1Bond>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18172000
MGI:5439494	M	MP:0004042	decreased susceptibility to kidney reperfusion injury	Mep1b<tm1Bond>/Mep1b<tm1Bond>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18172000
MGI:5439494	M	MP:0005566	decreased blood urea nitrogen level	Mep1b<tm1Bond>/Mep1b<tm1Bond>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	18172000
MGI:5439540	M	MP:0005389	reproductive system phenotype	Kpna1<tm1.2Yyo>/Kpna1<tm1.2Yyo>	involves: 129S2/SvPas * C57BL/6 * SJL	Y	21371262
MGI:5439540	F	MP:0031137	vaginal hemorrhage	Kpna1<tm1.2Yyo>/Kpna1<tm1.2Yyo>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21371262
MGI:5439540	F	MP:0004514	dystocia	Kpna1<tm1.2Yyo>/Kpna1<tm1.2Yyo>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21371262
MGI:5439540	F	MP:0003572	abnormal uterus development	Kpna1<tm1.2Yyo>/Kpna1<tm1.2Yyo>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21371262
MGI:5439540	F	MP:0002682	decreased mature ovarian follicle number	Kpna1<tm1.2Yyo>/Kpna1<tm1.2Yyo>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21371262
MGI:5439540	F	MP:0008028	pregnancy-related premature death	Kpna1<tm1.2Yyo>/Kpna1<tm1.2Yyo>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21371262
MGI:5439540	F	MP:0008257	thin myometrium	Kpna1<tm1.2Yyo>/Kpna1<tm1.2Yyo>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21371262
MGI:5439540	F	MP:0001120	abnormal uterus morphology	Kpna1<tm1.2Yyo>/Kpna1<tm1.2Yyo>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21371262
MGI:5439540	F	MP:0001935	decreased litter size	Kpna1<tm1.2Yyo>/Kpna1<tm1.2Yyo>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21371262
MGI:5439540	F	MP:0013400	abnormal endometrial gland development	Kpna1<tm1.2Yyo>/Kpna1<tm1.2Yyo>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21371262
MGI:5439540	F	MP:0005185	decreased circulating progesterone level	Kpna1<tm1.2Yyo>/Kpna1<tm1.2Yyo>	involves: 129S2/SvPas * C57BL/6 * SJL	N	21371262
MGI:5439605	F	MP:0004898	uterine hemorrhage	Prdm1<tm2Rob>/Prdm1<tm2Rob>	involves: 129S/SvEv	N	22987638
MGI:5439610	F	MP:0002169	no abnormal phenotype detected	Ubl4a<tm1Xya>/Ubl4a<tm1Xya>	involves: 129 * C57BL/6	N	22139977
MGI:5439611	M	MP:0002169	no abnormal phenotype detected	Ubl4a<tm1Xya>/Y	involves: 129 * C57BL/6	N	22139977
MGI:5439612	F	MP:0002169	no abnormal phenotype detected	Ubl4a<tm1.1Xya>/Ubl4a<tm1.1Xya>	involves: 129 * C57BL/6 * FVB/N	N	22139977
MGI:5439613	M	MP:0002169	no abnormal phenotype detected	Ubl4a<tm1.1Xya>/Y	involves: 129 * C57BL/6 * FVB/N	N	22139977
MGI:5439824	M	MP:0005389	reproductive system phenotype	Psen1<tm1.1Ruvi>/Psen1<tm1.1Ruvi>	C57BL/6J-Psen1<tm1.1Ruvi>	Y	22459153
MGI:5439824	F	MP:0001750	increased circulating follicle stimulating hormone level	Psen1<tm1.1Ruvi>/Psen1<tm1.1Ruvi>	C57BL/6J-Psen1<tm1.1Ruvi>	N	22459153
MGI:5439824	F	MP:0001126	abnormal ovary morphology	Psen1<tm1.1Ruvi>/Psen1<tm1.1Ruvi>	C57BL/6J-Psen1<tm1.1Ruvi>	N	22459153
MGI:5439824	F	MP:0001926	female infertility	Psen1<tm1.1Ruvi>/Psen1<tm1.1Ruvi>	C57BL/6J-Psen1<tm1.1Ruvi>	N	22459153
MGI:5439846	F	MP:0005431	decreased oocyte number	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	F	MP:0009362	abnormal primary ovarian follicle morphology	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	F	MP:0001126	abnormal ovary morphology	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	F	MP:0001125	abnormal oocyte morphology	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	F	MP:0001926	female infertility	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	F	MP:0013539	increased ovary adenoma incidence	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	M	MP:0001925	male infertility	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	M	MP:0001147	small testis	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	F	MP:0001127	small ovary	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	M	MP:0004852	decreased testis weight	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	M	MP:0005159	azoospermia	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	M	MP:0003205	testicular atrophy	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	F	MP:0001129	impaired ovarian folliculogenesis	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	M	MP:0001153	small seminiferous tubules	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	M	MP:0008280	abnormal male germ cell apoptosis	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	F	MP:0009092	endometrium hyperplasia	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	F	MP:0001132	absent mature ovarian follicles	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	F	MP:0008000	increased ovary tumor incidence	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	M	MP:0010948	abnormal double-strand DNA break repair	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439846	M	MP:0008261	arrest of male meiosis	Mcm8<tm1.1Geno>/Mcm8<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439847	F	MP:0001926	female infertility	Mcm9<tm1.1Geno>/Mcm9<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439847	M	MP:0005389	reproductive system phenotype	Mcm9<tm1.1Geno>/Mcm9<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	Y	22771120
MGI:5439847	M	MP:0008280	abnormal male germ cell apoptosis	Mcm9<tm1.1Geno>/Mcm9<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439847	M	MP:0002687	oligozoospermia	Mcm9<tm1.1Geno>/Mcm9<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5439847	M	MP:0002216	abnormal seminiferous tubule morphology	Mcm9<tm1.1Geno>/Mcm9<tm1.1Geno>	involves: 129S2/SvPas * C57BL/6J	N	22771120
MGI:5440078	F	MP:0002907	abnormal parturition	Bmal1<tm1.1Ljm>/Bmal1<tm1.1Ljm>,Tg(Mylk-cre)1Ljm/0	involves: C57BL/6	N	22697126
MGI:5440078	F	MP:0012008	delayed parturition	Bmal1<tm1.1Ljm>/Bmal1<tm1.1Ljm>,Tg(Mylk-cre)1Ljm/0	involves: C57BL/6	N	22697126
MGI:5440078	F	MP:0012009	early parturition	Bmal1<tm1.1Ljm>/Bmal1<tm1.1Ljm>,Tg(Mylk-cre)1Ljm/0	involves: C57BL/6	N	22697126
MGI:5440078	F	MP:0005376	homeostasis/metabolism phenotype	Bmal1<tm1.1Ljm>/Bmal1<tm1.1Ljm>,Tg(Mylk-cre)1Ljm/0	involves: C57BL/6	Y	22697126
MGI:5440238	M	MP:0001147	small testis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Stk11<tm1Rdp>/Stk11<tm1Rdp>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440238	M	MP:0001156	abnormal spermatogenesis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Stk11<tm1Rdp>/Stk11<tm1Rdp>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440238	M	MP:0031407	increased Sertoli cell proliferation	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Stk11<tm1Rdp>/Stk11<tm1Rdp>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440238	M	MP:0002784	abnormal Sertoli cell morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Stk11<tm1Rdp>/Stk11<tm1Rdp>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440238	M	MP:0004852	decreased testis weight	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Stk11<tm1Rdp>/Stk11<tm1Rdp>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440238	M	MP:0002216	abnormal seminiferous tubule morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Stk11<tm1Rdp>/Stk11<tm1Rdp>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440238	M	MP:0004901	decreased male germ cell number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Stk11<tm1Rdp>/Stk11<tm1Rdp>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440238	M	MP:0001146	abnormal testis morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Stk11<tm1Rdp>/Stk11<tm1Rdp>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440238	M	MP:0002006	neoplasm	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Stk11<tm1Rdp>/Stk11<tm1Rdp>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	Y	22791749
MGI:5440238	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Stk11<tm1Rdp>/Stk11<tm1Rdp>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440239	F	MP:0001728	failure of embryo implantation	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	F	MP:0009781	abnormal preimplantation embryo development	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	F	MP:0001926	female infertility	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	F	MP:0001125	abnormal oocyte morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	F	MP:0009012	short diestrus	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	F	MP:0031020	premature ovarian failure	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	F	MP:0009017	prolonged estrus	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	M	MP:0031407	increased Sertoli cell proliferation	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440239	M	MP:0004852	decreased testis weight	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440239	M	MP:0001146	abnormal testis morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440239	F	MP:0031239	increased atretic ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	M	MP:0001147	small testis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440239	F	MP:0011121	decreased primordial ovarian follicle number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	M	MP:0005389	reproductive system phenotype	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	Y	22128018
MGI:5440239	M	MP:0001156	abnormal spermatogenesis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440239	F	MP:0008256	abnormal myometrium morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	F	MP:0009069	dilated oviduct	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440239	F	MP:0002006	neoplasm	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	Y	22128018
MGI:5440239	F	MP:0003507	abnormal ovary physiology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	M	MP:0002006	neoplasm	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	Y	22791749
MGI:5440239	M	MP:0002216	abnormal seminiferous tubule morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440239	F	MP:0001129	impaired ovarian folliculogenesis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	M	MP:0002784	abnormal Sertoli cell morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440239	F	MP:0003574	abnormal oviduct morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	F	MP:0009093	oocyte degeneration	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	F	MP:0009092	endometrium hyperplasia	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22128018
MGI:5440239	M	MP:0004901	decreased male germ cell number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc1<tm1Djk>/Tsc1<tm1Djk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	N	22791749
MGI:5440240	M	MP:0004901	decreased male germ cell number	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	22791749
MGI:5440240	M	MP:0002006	neoplasm	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	Y	22791749
MGI:5440240	M	MP:0004852	decreased testis weight	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	22791749
MGI:5440240	M	MP:0001147	small testis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	22791749
MGI:5440240	M	MP:0002216	abnormal seminiferous tubule morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	22791749
MGI:5440240	M	MP:0001156	abnormal spermatogenesis	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	22791749
MGI:5440240	M	MP:0002784	abnormal Sertoli cell morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	22791749
MGI:5440240	M	MP:0001146	abnormal testis morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	22791749
MGI:5440240	M	MP:0031407	increased Sertoli cell proliferation	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	22791749
MGI:5440240	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	N	22791749
MGI:5440731	M	MP:0004997	increased CNS synapse formation	Nlgn3<tm1Rhn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22983708
MGI:5440731	M	MP:0004753	abnormal miniature excitatory postsynaptic currents	Nlgn3<tm1Rhn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22983708
MGI:5440731	M	MP:0011269	increased excitatory postsynaptic current amplitude	Nlgn3<tm1Rhn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22983708
MGI:5440731	M	MP:0001899	absent long-term depression	Nlgn3<tm1Rhn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22983708
MGI:5440731	M	MP:0001516	abnormal motor coordination/balance	Nlgn3<tm1Rhn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22983708
MGI:5440731	M	MP:0001900	impaired synaptic plasticity	Nlgn3<tm1Rhn>/Y	involves: 129S6/SvEvTac * C57BL/6	N	22983708
MGI:5440732	M	MP:0003631	nervous system phenotype	Nlgn3<tm1Rhn>/Y,Tg(Pcp2-tTA)3Horr/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	Y	22983708
MGI:5440902	M	MP:0001925	male infertility	Wnt7a<px-J>/Wnt7a<px-J>	C57BL/6J-Wnt7a<px-J>/GrsrJ	N	MGI:5440718
MGI:5440902	F	MP:0001926	female infertility	Wnt7a<px-J>/Wnt7a<px-J>	C57BL/6J-Wnt7a<px-J>/GrsrJ	N	MGI:5440718
MGI:5440902	M	MP:0002674	abnormal sperm motility	Wnt7a<px-J>/Wnt7a<px-J>	C57BL/6J-Wnt7a<px-J>/GrsrJ	N	MGI:5440718
MGI:5440925	M	MP:0001925	male infertility	Wnt7a<px-2J>/Wnt7a<px-2J>	B6;C3Fe-Wnt7a<px-2J>/GrsrJ	N	MGI:5440720
MGI:5440925	F	MP:0001926	female infertility	Wnt7a<px-2J>/Wnt7a<px-2J>	B6;C3Fe-Wnt7a<px-2J>/GrsrJ	N	MGI:5440720
MGI:5441019	M	MP:0002968	increased circulating alkaline phosphatase level	Hpn<Hlb320>/Hpn<Hlb320>	C57BL/6J-Hpn<Hlb320>/J	N	22912808
MGI:5441019	M	MP:0006325	impaired hearing	Hpn<Hlb320>/Hpn<Hlb320>	C57BL/6J-Hpn<Hlb320>/J	N	22912808
MGI:5441315	M	MP:0001432	abnormal food preference	Csk<tm1Sor>/Csk<+>	129P2.129S7-Csk<tm1Sor>	N	22348736
MGI:5441315	M	MP:0001458	abnormal object recognition memory	Csk<tm1Sor>/Csk<+>	129P2.129S7-Csk<tm1Sor>	N	22348736
MGI:5441315	M	MP:0001364	decreased anxiety-related response	Csk<tm1Sor>/Csk<+>	129P2.129S7-Csk<tm1Sor>	N	22348736
MGI:5441315	M	MP:0001360	abnormal social investigation	Csk<tm1Sor>/Csk<+>	129P2.129S7-Csk<tm1Sor>	N	22348736
MGI:5441342	M	MP:0002224	abnormal spleen size	Hbb-b1<tm1Unc>/Hbb-b1<+>,Hbb-b2<tm1Unc>/Hbb-b2<+>,Tmprss6<tm1Otin>/Tmprss6<+>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N	N	22490684
MGI:5441342	M	MP:0002591	decreased mean corpuscular volume	Hbb-b1<tm1Unc>/Hbb-b1<+>,Hbb-b2<tm1Unc>/Hbb-b2<+>,Tmprss6<tm1Otin>/Tmprss6<+>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N	N	22490684
MGI:5441342	M	MP:0008739	abnormal spleen iron level	Hbb-b1<tm1Unc>/Hbb-b1<+>,Hbb-b2<tm1Unc>/Hbb-b2<+>,Tmprss6<tm1Otin>/Tmprss6<+>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N	N	22490684
MGI:5441342	M	MP:0011284	abnormal circulating erythropoietin level	Hbb-b1<tm1Unc>/Hbb-b1<+>,Hbb-b2<tm1Unc>/Hbb-b2<+>,Tmprss6<tm1Otin>/Tmprss6<+>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N	N	22490684
MGI:5441342	M	MP:0005563	abnormal hemoglobin content	Hbb-b1<tm1Unc>/Hbb-b1<+>,Hbb-b2<tm1Unc>/Hbb-b2<+>,Tmprss6<tm1Otin>/Tmprss6<+>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N	N	22490684
MGI:5441342	M	MP:0002447	abnormal erythrocyte morphology	Hbb-b1<tm1Unc>/Hbb-b1<+>,Hbb-b2<tm1Unc>/Hbb-b2<+>,Tmprss6<tm1Otin>/Tmprss6<+>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N	N	22490684
MGI:5441342	M	MP:0008738	abnormal liver iron level	Hbb-b1<tm1Unc>/Hbb-b1<+>,Hbb-b2<tm1Unc>/Hbb-b2<+>,Tmprss6<tm1Otin>/Tmprss6<+>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N	N	22490684
MGI:5441538	F	MP:0004896	abnormal endometrium morphology	Gata4<tm1.2Wtp>/Gata4<+>	B6.Cg-Gata4<tm1.2Wtp>	N	21248289
MGI:5441538	F	MP:0004905	decreased uterus weight	Gata4<tm1.2Wtp>/Gata4<+>	B6.Cg-Gata4<tm1.2Wtp>	N	21248289
MGI:5441538	F	MP:0001938	delayed sexual maturation	Gata4<tm1.2Wtp>/Gata4<+>	B6.Cg-Gata4<tm1.2Wtp>	N	21248289
MGI:5441538	F	MP:0005389	reproductive system phenotype	Gata4<tm1.2Wtp>/Gata4<+>	B6.Cg-Gata4<tm1.2Wtp>	Y	21248289
MGI:5441538	F	MP:0004856	decreased ovary weight	Gata4<tm1.2Wtp>/Gata4<+>	B6.Cg-Gata4<tm1.2Wtp>	N	21248289
MGI:5441538	F	MP:0031420	decreased superovulation rate	Gata4<tm1.2Wtp>/Gata4<+>	B6.Cg-Gata4<tm1.2Wtp>	N	21248289
MGI:5441538	F	MP:0009008	delayed estrous cycle	Gata4<tm1.2Wtp>/Gata4<+>	B6.Cg-Gata4<tm1.2Wtp>	N	21248289
MGI:5441538	F	MP:0001127	small ovary	Gata4<tm1.2Wtp>/Gata4<+>	B6.Cg-Gata4<tm1.2Wtp>	N	21248289
MGI:5441538	F	MP:0003507	abnormal ovary physiology	Gata4<tm1.2Wtp>/Gata4<+>	B6.Cg-Gata4<tm1.2Wtp>	N	21248289
MGI:5441538	F	MP:0005181	decreased circulating estradiol level	Gata4<tm1.2Wtp>/Gata4<+>	B6.Cg-Gata4<tm1.2Wtp>	N	21248289
MGI:5441570	M	MP:0001147	small testis	Hsp90aa1<tm1.1Udon>/Hsp90aa1<tm1.1Udon>	involves: C57BL/6 * FVB	N	23213375
MGI:5441570	M	MP:0003609	small scrotum	Hsp90aa1<tm1.1Udon>/Hsp90aa1<tm1.1Udon>	involves: C57BL/6 * FVB	N	23213375
MGI:5441570	M	MP:0001925	male infertility	Hsp90aa1<tm1.1Udon>/Hsp90aa1<tm1.1Udon>	involves: C57BL/6 * FVB	N	23213375
MGI:5441570	M	MP:0014052	increased male germ cell apoptosis	Hsp90aa1<tm1.1Udon>/Hsp90aa1<tm1.1Udon>	involves: C57BL/6 * FVB	N	23213375
MGI:5441570	M	MP:0005159	azoospermia	Hsp90aa1<tm1.1Udon>/Hsp90aa1<tm1.1Udon>	involves: C57BL/6 * FVB	N	23213375
MGI:5441737	F	MP:0010771	integument phenotype	Atp7a<Mo-3Btlr>/Atp7a<+>	C57BL/6J-Atp7a<Mo-3Btlr>	Y	22869751
MGI:5442747	M	MP:0000621	increased salivary adenocarcinoma incidence	Pten<tm1Rps>/Pten<+>,Tg(Wnt1)1Hev/0	involves: 129S1/Sv * C57BL/6 * FVB/N * SJL	N	11178110
MGI:5444176	F	MP:0000689	abnormal spleen morphology	Pi4ka<tm2.1Arte>/Pi4ka<+>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6NTac	N	22896614
MGI:5444176	M	MP:0001262	decreased body weight	Pi4ka<tm2.1Arte>/Pi4ka<+>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6NTac	N	22896614
MGI:5444176	M	MP:0001510	abnormal coat appearance	Pi4ka<tm2.1Arte>/Pi4ka<+>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6NTac	N	22896614
MGI:5444176	M	MP:0000462	abnormal digestive system morphology	Pi4ka<tm2.1Arte>/Pi4ka<+>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6NTac	N	22896614
MGI:5444176	M	MP:0002083	premature death	Pi4ka<tm2.1Arte>/Pi4ka<+>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6NTac	N	22896614
MGI:5444176	M	MP:0001505	hunched posture	Pi4ka<tm2.1Arte>/Pi4ka<+>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6NTac	N	22896614
MGI:5444194	F	MP:0009010	abnormal diestrus	Pparg<tm2Rev>/Pparg<tm2Rev>,Tg(Lhb-cre)1Sac/?	involves: 129S4/SvJae * C57BL/6 * SJL	N	21076077
MGI:5444194	F	MP:0005133	increased luteinizing hormone level	Pparg<tm2Rev>/Pparg<tm2Rev>,Tg(Lhb-cre)1Sac/?	involves: 129S4/SvJae * C57BL/6 * SJL	N	21076077
MGI:5444194	M	MP:0002790	decreased circulating follicle stimulating hormone level	Pparg<tm2Rev>/Pparg<tm2Rev>,Tg(Lhb-cre)1Sac/?	involves: 129S4/SvJae * C57BL/6 * SJL	N	21076077
MGI:5444514	M	MP:0000519	hydronephrosis	Elp1<tm1Id>/Elp1<tm1Id>,Tg(Hsp70-1-cre)6Arge/0	involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA	N	22922231
MGI:5444514	M	MP:0005302	neurogenic bladder	Elp1<tm1Id>/Elp1<tm1Id>,Tg(Hsp70-1-cre)6Arge/0	involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA	N	22922231
MGI:5444514	M	MP:0000539	distended urinary bladder	Elp1<tm1Id>/Elp1<tm1Id>,Tg(Hsp70-1-cre)6Arge/0	involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA	N	22922231
MGI:5444635	M	MP:0000539	distended urinary bladder	Elp1<tm1Id>/Elp1<tm1.1Id>,Tg(Hsp70-1-cre)6Arge/0	involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA	N	22922231
MGI:5444635	M	MP:0000519	hydronephrosis	Elp1<tm1Id>/Elp1<tm1.1Id>,Tg(Hsp70-1-cre)6Arge/0	involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA	N	22922231
MGI:5444635	M	MP:0005302	neurogenic bladder	Elp1<tm1Id>/Elp1<tm1.1Id>,Tg(Hsp70-1-cre)6Arge/0	involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA	N	22922231
MGI:5444639	M	MP:0001800	abnormal humoral immune response	Sh2d1a<tm2.1Cpt>/Y,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	22613797
MGI:5444639	M	MP:0001805	decreased IgG level	Sh2d1a<tm2.1Cpt>/Y,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	22613797
MGI:5444639	M	MP:0001806	decreased IgM level	Sh2d1a<tm2.1Cpt>/Y,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	22613797
MGI:5444639	M	MP:0008192	abnormal germinal center B cell physiology	Sh2d1a<tm2.1Cpt>/Y,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	22613797
MGI:5444639	M	MP:0005387	immune system phenotype	Sh2d1a<tm2.1Cpt>/Y,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	Y	22613797
MGI:5444640	F	MP:0001805	decreased IgG level	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>,Tcra-J<tm1Tgi>/Tcra-J<tm1Tgi>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/c	N	22613797
MGI:5444640	F	MP:0008178	decreased germinal center B cell number	Sh2d1a<tm1Cpt>/Sh2d1a<tm1Cpt>,Tcra-J<tm1Tgi>/Tcra-J<tm1Tgi>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/c	N	22613797
MGI:5444641	F	MP:0001805	decreased IgG level	Sh2d1a<tm2.1Cpt>/Sh2d1a<tm2.1Cpt>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	22613797
MGI:5444641	F	MP:0005387	immune system phenotype	Sh2d1a<tm2.1Cpt>/Sh2d1a<tm2.1Cpt>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	Y	22613797
MGI:5444641	F	MP:0001800	abnormal humoral immune response	Sh2d1a<tm2.1Cpt>/Sh2d1a<tm2.1Cpt>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	22613797
MGI:5444641	F	MP:0001806	decreased IgM level	Sh2d1a<tm2.1Cpt>/Sh2d1a<tm2.1Cpt>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	22613797
MGI:5444641	F	MP:0008192	abnormal germinal center B cell physiology	Sh2d1a<tm2.1Cpt>/Sh2d1a<tm2.1Cpt>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	22613797
MGI:5444642	M	MP:0002490	abnormal immunoglobulin level	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * C57BL/6	N	22613797
MGI:5444642	M	MP:0008040	decreased NK T cell number	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * C57BL/6	N	22613797
MGI:5444642	M	MP:0008042	abnormal NK T cell physiology	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * C57BL/6	N	22613797
MGI:5444642	M	MP:0003009	abnormal cytokine secretion	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * C57BL/6	N	11323694
MGI:5444642	M	MP:0020913	increased susceptibility to Riboviria infection	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * C57BL/6	N	11323694
MGI:5444642	M	MP:0008192	abnormal germinal center B cell physiology	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * C57BL/6	N	22613797
MGI:5444642	M	MP:0005348	increased T cell proliferation	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * C57BL/6	N	11323694
MGI:5444642	M	MP:0001800	abnormal humoral immune response	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * C57BL/6	N	22613797
MGI:5444643	M	MP:0008040	decreased NK T cell number	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * BALB/c	N	22613797
MGI:5444643	M	MP:0002492	decreased IgE level	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * BALB/c	N	11323694
MGI:5444643	M	MP:0005026	decreased susceptibility to parasitic infection	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * BALB/c	N	11323694
MGI:5444643	M	MP:0008178	decreased germinal center B cell number	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * BALB/c	N	22613797
MGI:5444643	M	MP:0008176	abnormal germinal center B cell morphology	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * BALB/c	N	22613797
MGI:5444643	M	MP:0001805	decreased IgG level	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * BALB/c	N	22613797
MGI:5444643	M	MP:0003009	abnormal cytokine secretion	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * BALB/c	N	11323694
MGI:5444643	M	MP:0005387	immune system phenotype	Sh2d1a<tm1Cpt>/Y	involves: 129S4/SvJae * BALB/c	Y	22613797
MGI:5444644	M	MP:0001805	decreased IgG level	Sh2d1a<tm1Cpt>/Y,Tcra-J<tm1Tgi>/Tcra-J<tm1Tgi>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/c	N	22613797
MGI:5444644	M	MP:0008178	decreased germinal center B cell number	Sh2d1a<tm1Cpt>/Y,Tcra-J<tm1Tgi>/Tcra-J<tm1Tgi>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/c	N	22613797
MGI:5444650	F	MP:0009664	abnormal luminal closure	Ncoa6<tm3Jxu>/Ncoa6<tm3Jxu>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129/Sv * C57BL/6 * SJL	N	23079602
MGI:5444650	F	MP:0001926	female infertility	Ncoa6<tm3Jxu>/Ncoa6<tm3Jxu>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129/Sv * C57BL/6 * SJL	N	23079602
MGI:5444650	F	MP:0003845	abnormal decidualization	Ncoa6<tm3Jxu>/Ncoa6<tm3Jxu>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129/Sv * C57BL/6 * SJL	N	23079602
MGI:5444650	F	MP:0009662	abnormal uterine receptivity	Ncoa6<tm3Jxu>/Ncoa6<tm3Jxu>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129/Sv * C57BL/6 * SJL	N	23079602
MGI:5444860	M	MP:0002796	impaired skin barrier function	Tg(KRT14-Prss8)1Hum/?	involves: C57BL/6 * DBA/2	N	21245842
MGI:5444860	M	MP:0001243	abnormal dermal layer morphology	Tg(KRT14-Prss8)1Hum/?	involves: C57BL/6 * DBA/2	N	21245842
MGI:5444860	M	MP:0001874	acanthosis	Tg(KRT14-Prss8)1Hum/?	involves: C57BL/6 * DBA/2	N	21245842
MGI:5444860	M	MP:0001262	decreased body weight	Tg(KRT14-Prss8)1Hum/?	involves: C57BL/6 * DBA/2	N	21245842
MGI:5444860	M	MP:0001192	scaly skin	Tg(KRT14-Prss8)1Hum/?	involves: C57BL/6 * DBA/2	N	21245842
MGI:5444860	M	MP:0001212	skin lesions	Tg(KRT14-Prss8)1Hum/?	involves: C57BL/6 * DBA/2	N	21245842
MGI:5444860	M	MP:0000416	sparse hair	Tg(KRT14-Prss8)1Hum/?	involves: C57BL/6 * DBA/2	N	21245842
MGI:5444860	M	MP:0009596	abnormal stratum corneum lipid matrix formation	Tg(KRT14-Prss8)1Hum/?	involves: C57BL/6 * DBA/2	N	21245842
MGI:5444860	M	MP:0001412	excessive scratching	Tg(KRT14-Prss8)1Hum/?	involves: C57BL/6 * DBA/2	N	21245842
MGI:5445702	F	MP:0001935	decreased litter size	Slc2a8<tm1Khm>/Slc2a8<+>	involves: 129X1/SvJ	N	22822162
MGI:5445703	F	MP:0001668	abnormal intestinal fructose absorption	Tg(ACTB-Slc2a12)#Khm/0	involves: FVB/NJ	N	22822162
MGI:5445717	F	MP:0001927	abnormal estrous cycle	Insl5<tm1Imad>/Insl5<tm1Imad>	129(B6)-Insl5<tm1Imad>	N	22822165
MGI:5445717	M	MP:0001922	reduced male fertility	Insl5<tm1Imad>/Insl5<tm1Imad>	129(B6)-Insl5<tm1Imad>	N	22822165
MGI:5445717	F	MP:0001923	reduced female fertility	Insl5<tm1Imad>/Insl5<tm1Imad>	129(B6)-Insl5<tm1Imad>	N	22822165
MGI:5445717	M	MP:0001925	male infertility	Insl5<tm1Imad>/Insl5<tm1Imad>	129(B6)-Insl5<tm1Imad>	N	22822165
MGI:5445717	M	MP:0002675	asthenozoospermia	Insl5<tm1Imad>/Insl5<tm1Imad>	129(B6)-Insl5<tm1Imad>	N	22822165
MGI:5445717	F	MP:0001926	female infertility	Insl5<tm1Imad>/Insl5<tm1Imad>	129(B6)-Insl5<tm1Imad>	N	22822165
MGI:5445746	F	MP:0005389	reproductive system phenotype	Cdx2<tm1.1Aral>/Cdx2<tm1.1Aral>,Tg(Zp3-cre)93Knw/0	involves: 129X1/SvJ * C57BL/6 * CD-1 * SJL	Y	22992952
MGI:5445747	F	MP:0005389	reproductive system phenotype	Cdx2<tm1.1Aral>/Cdx2<tm1.2Aral>,Tg(Zp3-cre)93Knw/0	involves: 129X1/SvJ * C57BL/6 * CD-1 * SJL	Y	22992952
MGI:5445965	F	MP:0001258	decreased body length	Raf1<tm2.1Ara>/Raf1<+>	involves: 129S6/SvEvTac * C57BL/6NCr	N	22826437
MGI:5446039	M	MP:0005123	increased circulating growth hormone level	Mex3c<Gt(DD0642)Wtsi>/Mex3c<Gt(DD0642)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	22357625
MGI:5446041	F	MP:0008831	abnormal insulin-like growth factor I level	Mex3c<Gt(DD0642)Wtsi>/Mex3c<Gt(DD0642)Wtsi>	FVB.129P2(B6)-Mex3c<Gt(DD0642)Wtsi>	N	22357625
MGI:5446136	M	MP:0011703	increased fibroblast proliferation	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	23267082
MGI:5446136	M	MP:0000609	abnormal liver physiology	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	23267082
MGI:5446136	M	MP:0001792	impaired wound healing	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	23267082
MGI:5446136	M	MP:0003077	abnormal cell cycle	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	23267082
MGI:5446136	M	MP:0020470	shortened circadian behavior period	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	23267082
MGI:5446136	M	MP:0020470	shortened circadian behavior period	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	22966205
MGI:5446136	M	MP:0008009	delayed cellular replicative senescence	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	23267082
MGI:5446493	M	MP:0003059	decreased insulin secretion	Gck<Gls006>/Gck<+>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:5446493	M	MP:0001559	hyperglycemia	Gck<Gls006>/Gck<+>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:5446493	M	MP:0002727	decreased circulating insulin level	Gck<Gls006>/Gck<+>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:5446493	M	MP:0005293	impaired glucose tolerance	Gck<Gls006>/Gck<+>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:5446493	M	MP:0005376	homeostasis/metabolism phenotype	Gck<Gls006>/Gck<+>	C3HeB/FeJ-Gck<Gls006>	Y	22698525
MGI:5446493	M	MP:0005559	increased circulating glucose level	Gck<Gls006>/Gck<+>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:5446493	M	MP:0009114	decreased pancreatic beta cell mass	Gck<Gls006>/Gck<+>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:5446493	M	MP:0009172	small pancreatic islets	Gck<Gls006>/Gck<+>	C3HeB/FeJ-Gck<Gls006>	N	22698525
MGI:5446724	F	MP:0011939	increased food intake	Gpr26<tm1Yugs>/Gpr26<tm1Yugs>	involves: C57BL/6	N	22815809
MGI:5446724	F	MP:0005178	increased circulating cholesterol level	Gpr26<tm1Yugs>/Gpr26<tm1Yugs>	involves: C57BL/6	N	22815809
MGI:5446724	F	MP:0005293	impaired glucose tolerance	Gpr26<tm1Yugs>/Gpr26<tm1Yugs>	involves: C57BL/6	N	22815809
MGI:5446724	F	MP:0004890	decreased energy expenditure	Gpr26<tm1Yugs>/Gpr26<tm1Yugs>	involves: C57BL/6	N	22815809
MGI:5446724	F	MP:0005559	increased circulating glucose level	Gpr26<tm1Yugs>/Gpr26<tm1Yugs>	involves: C57BL/6	N	22815809
MGI:5446724	F	MP:0001552	increased circulating triglyceride level	Gpr26<tm1Yugs>/Gpr26<tm1Yugs>	involves: C57BL/6	N	22815809
MGI:5446724	F	MP:0008873	increased physiological sensitivity to xenobiotic	Gpr26<tm1Yugs>/Gpr26<tm1Yugs>	involves: C57BL/6	N	22815809
MGI:5446724	F	MP:0005669	increased circulating leptin level	Gpr26<tm1Yugs>/Gpr26<tm1Yugs>	involves: C57BL/6	N	22815809
MGI:5446724	F	MP:0005658	increased susceptibility to diet-induced obesity	Gpr26<tm1Yugs>/Gpr26<tm1Yugs>	involves: C57BL/6	N	22815809
MGI:5446724	F	MP:0010024	increased total body fat amount	Gpr26<tm1Yugs>/Gpr26<tm1Yugs>	involves: C57BL/6	N	22815809
MGI:5446745	M	MP:0001925	male infertility	Del(Y)2H/?	mixed	N	8275095
MGI:5446745	M	MP:0008261	arrest of male meiosis	Del(Y)2H/?	mixed	N	8275095
MGI:5446745	M	MP:0001147	small testis	Del(Y)2H/?	mixed	N	8275095
MGI:5446773	M	MP:0001925	male infertility	Pank2<tm1.1Suja>/Pank2<tm1.1Suja>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	22815849
MGI:5446773	M	MP:0001147	small testis	Pank2<tm1.1Suja>/Pank2<tm1.1Suja>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	22815849
MGI:5446773	M	MP:0005159	azoospermia	Pank2<tm1.1Suja>/Pank2<tm1.1Suja>	involves: 129S/SvEv * C57BL/6J * FVB/N	N	22815849
MGI:5446815	M	MP:0008261	arrest of male meiosis	Del(Y)3H/?	mixed	N	8275095
MGI:5446815	M	MP:0001925	male infertility	Del(Y)3H/?	mixed	N	8275095
MGI:5446815	M	MP:0001147	small testis	Del(Y)3H/?	mixed	N	8275095
MGI:5447008	F	MP:0014126	increased mammary gland apoptosis	Erbb3<tm1.1(ERBB3)Mul>/Erbb3<tm1.1(ERBB3)Mul>	FVB.129P2(Cg)-Erbb3<tm1.1(ERBB3)Mul>	N	22665265
MGI:5447008	F	MP:0009504	abnormal mammary gland epithelium morphology	Erbb3<tm1.1(ERBB3)Mul>/Erbb3<tm1.1(ERBB3)Mul>	FVB.129P2(Cg)-Erbb3<tm1.1(ERBB3)Mul>	N	22665265
MGI:5447008	F	MP:0009503	abnormal mammary gland duct morphology	Erbb3<tm1.1(ERBB3)Mul>/Erbb3<tm1.1(ERBB3)Mul>	FVB.129P2(Cg)-Erbb3<tm1.1(ERBB3)Mul>	N	22665265
MGI:5447008	F	MP:0013716	hypolactation	Erbb3<tm1.1(ERBB3)Mul>/Erbb3<tm1.1(ERBB3)Mul>	FVB.129P2(Cg)-Erbb3<tm1.1(ERBB3)Mul>	N	22665265
MGI:5447008	F	MP:0006271	abnormal involution of the mammary gland	Erbb3<tm1.1(ERBB3)Mul>/Erbb3<tm1.1(ERBB3)Mul>	FVB.129P2(Cg)-Erbb3<tm1.1(ERBB3)Mul>	N	22665265
MGI:5447008	F	MP:0006270	abnormal mammary gland growth during lactation	Erbb3<tm1.1(ERBB3)Mul>/Erbb3<tm1.1(ERBB3)Mul>	FVB.129P2(Cg)-Erbb3<tm1.1(ERBB3)Mul>	N	22665265
MGI:5447008	F	MP:0009506	abnormal mammary gland alveolus morphology	Erbb3<tm1.1(ERBB3)Mul>/Erbb3<tm1.1(ERBB3)Mul>	FVB.129P2(Cg)-Erbb3<tm1.1(ERBB3)Mul>	N	22665265
MGI:5447473	F	MP:0004610	small vertebrae	Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<tm1(Pyy)Paba>	involves: 129S4/SvJae	N	22792209
MGI:5447473	F	MP:0010879	decreased trabecular bone volume	Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<tm1(Pyy)Paba>	involves: 129S4/SvJae	N	22792209
MGI:5447473	F	MP:0020010	decreased bone mineral density of femur	Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<tm1(Pyy)Paba>	involves: 129S4/SvJae	N	22792209
MGI:5447473	F	MP:0004991	decreased bone strength	Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<tm1(Pyy)Paba>	involves: 129S4/SvJae	N	22792209
MGI:5447473	F	MP:0003109	short femur	Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<tm1(Pyy)Paba>	involves: 129S4/SvJae	N	22792209
MGI:5447473	F	MP:0010968	decreased compact bone area	Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<tm1(Pyy)Paba>	involves: 129S4/SvJae	N	22792209
MGI:5447473	F	MP:0003961	decreased lean body mass	Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<tm1(Pyy)Paba>	involves: 129S4/SvJae	N	22792209
MGI:5447473	F	MP:0004984	increased osteoclast cell number	Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<tm1(Pyy)Paba>	involves: 129S4/SvJae	N	22792209
MGI:5447642	M	MP:0009901	abnormal frontonasal prominence morphology	Atp7a<tm1.1Mjp>/Y,Cldn6<tm1(cre)Dkwu>/Cldn6<+>	involves: C57BL/6	N	22900086
MGI:5447642	M	MP:0003717	pallor	Atp7a<tm1.1Mjp>/Y,Cldn6<tm1(cre)Dkwu>/Cldn6<+>	involves: C57BL/6	N	22900086
MGI:5447642	M	MP:0002861	abnormal tail bud morphology	Atp7a<tm1.1Mjp>/Y,Cldn6<tm1(cre)Dkwu>/Cldn6<+>	involves: C57BL/6	N	22900086
MGI:5447642	M	MP:0001698	decreased embryo size	Atp7a<tm1.1Mjp>/Y,Cldn6<tm1(cre)Dkwu>/Cldn6<+>	involves: C57BL/6	N	22900086
MGI:5447642	M	MP:0001722	pale yolk sac	Atp7a<tm1.1Mjp>/Y,Cldn6<tm1(cre)Dkwu>/Cldn6<+>	involves: C57BL/6	N	22900086
MGI:5447642	M	MP:0011091	prenatal lethality, complete penetrance	Atp7a<tm1.1Mjp>/Y,Cldn6<tm1(cre)Dkwu>/Cldn6<+>	involves: C57BL/6	N	22900086
MGI:5447643	F	MP:0011086	postnatal lethality, incomplete penetrance	Atp7a<tm1.1Mjp>/Atp7a<+>,Cldn6<tm1(cre)Dkwu>/Cldn6<+>	involves: C57BL/6	N	22900086
MGI:5447643	F	MP:0011101	prenatal lethality, incomplete penetrance	Atp7a<tm1.1Mjp>/Atp7a<+>,Cldn6<tm1(cre)Dkwu>/Cldn6<+>	involves: C57BL/6	N	22900086
MGI:5447643	F	MP:0005408	hypopigmentation	Atp7a<tm1.1Mjp>/Atp7a<+>,Cldn6<tm1(cre)Dkwu>/Cldn6<+>	involves: C57BL/6	N	22900086
MGI:5447643	F	MP:0001274	curly vibrissae	Atp7a<tm1.1Mjp>/Atp7a<+>,Cldn6<tm1(cre)Dkwu>/Cldn6<+>	involves: C57BL/6	N	22900086
MGI:5447979	M	MP:0001146	abnormal testis morphology	Hhat<Tg(TFAP2A-cre)1Will>/Hhat<Tg(TFAP2A-cre)1Will>	Not Specified	N	24784881
MGI:5447979	M	MP:0006418	abnormal testis cord formation	Hhat<Tg(TFAP2A-cre)1Will>/Hhat<Tg(TFAP2A-cre)1Will>	Not Specified	N	24784881
MGI:5447979	M	MP:0001147	small testis	Hhat<Tg(TFAP2A-cre)1Will>/Hhat<Tg(TFAP2A-cre)1Will>	Not Specified	N	24784881
MGI:5447979	M	MP:0013603	abnormal fetal Leydig cell differentiation	Hhat<Tg(TFAP2A-cre)1Will>/Hhat<Tg(TFAP2A-cre)1Will>	Not Specified	N	24784881
MGI:5447979	M	MP:0003830	abnormal testis development	Hhat<Tg(TFAP2A-cre)1Will>/Hhat<Tg(TFAP2A-cre)1Will>	Not Specified	N	24784881
MGI:5448209	M	MP:0031391	increased locomotor activity	Tg(NES/TK-PDGFB,-lacZ)310Kfn/0	involves: C57BL/6 * CBA	N	20643125
MGI:5448209	M	MP:0001415	increased exploration in new environment	Tg(NES/TK-PDGFB,-lacZ)310Kfn/0	involves: C57BL/6 * CBA	N	20643125
MGI:5448209	M	MP:0003312	abnormal locomotor coordination	Tg(NES/TK-PDGFB,-lacZ)310Kfn/0	involves: C57BL/6 * CBA	N	20643125
MGI:5448415	M	MP:0005386	behavior/neurological phenotype	Slc6a8<tm1.1Clar>/Y,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6 * C57BL/6J * FVB/N	Y	22751104
MGI:5448415	M	MP:0001399	hyperactivity	Slc6a8<tm1.1Clar>/Y,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6 * C57BL/6J * FVB/N	N	22751104
MGI:5448415	M	MP:0003461	abnormal response to novel object	Slc6a8<tm1.1Clar>/Y,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6 * C57BL/6J * FVB/N	N	22751104
MGI:5448415	M	MP:0008428	abnormal spatial working memory	Slc6a8<tm1.1Clar>/Y,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6 * C57BL/6J * FVB/N	N	22751104
MGI:5448415	M	MP:0005459	decreased percent body fat/body weight	Slc6a8<tm1.1Clar>/Y,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6 * C57BL/6J * FVB/N	N	22751104
MGI:5448415	M	MP:0010062	decreased creatine level	Slc6a8<tm1.1Clar>/Y,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6 * C57BL/6J * FVB/N	N	22751104
MGI:5448415	M	MP:0001463	abnormal spatial learning	Slc6a8<tm1.1Clar>/Y,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6 * C57BL/6J * FVB/N	N	22751104
MGI:5448415	M	MP:0008414	abnormal spatial reference memory	Slc6a8<tm1.1Clar>/Y,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6 * C57BL/6J * FVB/N	N	22751104
MGI:5448415	M	MP:0030632	increased urine creatine level	Slc6a8<tm1.1Clar>/Y,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6 * C57BL/6J * FVB/N	N	22751104
MGI:5448537	M	MP:0008596	increased circulating interleukin-6 level	Mir122<tm1.2Kgh>/Mir122<tm1.2Kgh>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA	N	22820288
MGI:5448537	M	MP:0008705	increased interleukin-6 secretion	Mir122<tm1.2Kgh>/Mir122<tm1.2Kgh>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA	N	22820288
MGI:5448537	F	MP:0003331	increased hepatocellular carcinoma incidence	Mir122<tm1.2Kgh>/Mir122<tm1.2Kgh>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA	N	22820288
MGI:5448537	M	MP:0008019	increased liver tumor incidence	Mir122<tm1.2Kgh>/Mir122<tm1.2Kgh>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA	N	22820288
MGI:5448538	M	MP:0008596	increased circulating interleukin-6 level	Mir122<tm1.1Kgh>/Mir122<tm1.1Kgh>	involves: 129S1/Sv * 129X1/SvJ	N	22820288
MGI:5448538	M	MP:0003721	increased tumor growth/size	Mir122<tm1.1Kgh>/Mir122<tm1.1Kgh>	involves: 129S1/Sv * 129X1/SvJ	N	22820288
MGI:5448696	M	MP:0003059	decreased insulin secretion	Akap5<tm1Mdaq>/Akap5<tm1Mdaq>	involves: 129 * C57BL/6 * C57BL/6J	N	22940692
MGI:5448696	M	MP:0002727	decreased circulating insulin level	Akap5<tm1Mdaq>/Akap5<tm1Mdaq>	involves: 129 * C57BL/6 * C57BL/6J	N	22940692
MGI:5448696	M	MP:0002891	increased insulin sensitivity	Akap5<tm1Mdaq>/Akap5<tm1Mdaq>	involves: 129 * C57BL/6 * C57BL/6J	N	22940692
MGI:5448696	M	MP:0005292	improved glucose tolerance	Akap5<tm1Mdaq>/Akap5<tm1Mdaq>	involves: 129 * C57BL/6 * C57BL/6J	N	22940692
MGI:5448699	M	MP:0005293	impaired glucose tolerance	Akap5<tm1Jsco>/Akap5<tm1Jsco>,Tg(Ins2-cre)25Mgn/0	involves: 129S * C57BL/6 * DBA	N	22940692
MGI:5448699	M	MP:0003058	increased insulin secretion	Akap5<tm1Jsco>/Akap5<tm1Jsco>,Tg(Ins2-cre)25Mgn/0	involves: 129S * C57BL/6 * DBA	N	22940692
MGI:5448699	M	MP:0002727	decreased circulating insulin level	Akap5<tm1Jsco>/Akap5<tm1Jsco>,Tg(Ins2-cre)25Mgn/0	involves: 129S * C57BL/6 * DBA	N	22940692
MGI:5448700	M	MP:0002727	decreased circulating insulin level	Akap5<tm1Gsm>/Akap5<tm1Gsm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	22940692
MGI:5448700	M	MP:0005376	homeostasis/metabolism phenotype	Akap5<tm1Gsm>/Akap5<tm1Gsm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	22940692
MGI:5448701	M	MP:0005292	improved glucose tolerance	Akap5<tm1.1Jsco>/Akap5<tm1.1Jsco>	involves: 129S * C57BL/6	N	22940692
MGI:5448701	M	MP:0003059	decreased insulin secretion	Akap5<tm1.1Jsco>/Akap5<tm1.1Jsco>	involves: 129S * C57BL/6	N	22940692
MGI:5448701	M	MP:0005217	abnormal pancreatic beta cell morphology	Akap5<tm1.1Jsco>/Akap5<tm1.1Jsco>	involves: 129S * C57BL/6	N	22940692
MGI:5448701	M	MP:0002727	decreased circulating insulin level	Akap5<tm1.1Jsco>/Akap5<tm1.1Jsco>	involves: 129S * C57BL/6	N	22940692
MGI:5448701	M	MP:0002891	increased insulin sensitivity	Akap5<tm1.1Jsco>/Akap5<tm1.1Jsco>	involves: 129S * C57BL/6	N	22940692
MGI:5448829	F	MP:0002169	no abnormal phenotype detected	Kdm6a<tm1.1Kaig>/Kdm6a<tm1.1Kaig>	involves: 129S4/SvJaeSor	N	22949634
MGI:5448830	F	MP:0003720	abnormal neural tube closure	Kdm6a<tm1.2Kaig>/Kdm6a<tm1.2Kaig>	involves: 129S4/SvJaeSor * C57BL/6 * FVB/N	N	22949634
MGI:5448830	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Kdm6a<tm1.2Kaig>/Kdm6a<tm1.2Kaig>	involves: 129S4/SvJaeSor * C57BL/6 * FVB/N	N	22949634
MGI:5448830	F	MP:0000267	abnormal heart development	Kdm6a<tm1.2Kaig>/Kdm6a<tm1.2Kaig>	involves: 129S4/SvJaeSor * C57BL/6 * FVB/N	N	22949634
MGI:5448830	F	MP:0005221	abnormal rostral-caudal axis patterning	Kdm6a<tm1.2Kaig>/Kdm6a<tm1.2Kaig>	involves: 129S4/SvJaeSor * C57BL/6 * FVB/N	N	22949634
MGI:5448830	F	MP:0001577	anemia	Kdm6a<tm1.2Kaig>/Kdm6a<tm1.2Kaig>	involves: 129S4/SvJaeSor * C57BL/6 * FVB/N	N	22949634
MGI:5448830	F	MP:0002825	abnormal notochord morphology	Kdm6a<tm1.2Kaig>/Kdm6a<tm1.2Kaig>	involves: 129S4/SvJaeSor * C57BL/6 * FVB/N	N	22949634
MGI:5448830	F	MP:0004073	caudal body truncation	Kdm6a<tm1.2Kaig>/Kdm6a<tm1.2Kaig>	involves: 129S4/SvJaeSor * C57BL/6 * FVB/N	N	22949634
MGI:5448831	M	MP:0011089	perinatal lethality, complete penetrance	Kdm6a<tm1.2Kaig>/Y	involves: 129S4/SvJaeSor	N	22949634
MGI:5448831	M	MP:0001177	atelectasis	Kdm6a<tm1.2Kaig>/Y	involves: 129S4/SvJaeSor	N	22949634
MGI:5448831	M	MP:0005380	embryo phenotype	Kdm6a<tm1.2Kaig>/Y	involves: 129S4/SvJaeSor	Y	22949634
MGI:5448831	M	MP:0000914	exencephaly	Kdm6a<tm1.2Kaig>/Y	involves: 129S4/SvJaeSor	N	22949634
MGI:5448831	M	MP:0001954	respiratory distress	Kdm6a<tm1.2Kaig>/Y	involves: 129S4/SvJaeSor	N	22949634
MGI:5448831	M	MP:0003720	abnormal neural tube closure	Kdm6a<tm1.2Kaig>/Y	involves: 129S4/SvJaeSor	N	22949634
MGI:5449045	M	MP:0004901	decreased male germ cell number	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	27666520
MGI:5449045	M	MP:0001935	decreased litter size	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0001922	reduced male fertility	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0001147	small testis	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0001147	small testis	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	27666520
MGI:5449045	M	MP:0001156	abnormal spermatogenesis	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0005389	reproductive system phenotype	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	Y	27666520
MGI:5449045	M	MP:0005389	reproductive system phenotype	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	Y	24371141
MGI:5449045	M	MP:0002662	abnormal cauda epididymis morphology	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0001153	small seminiferous tubules	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	27666520
MGI:5449045	M	MP:0001153	small seminiferous tubules	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0004852	decreased testis weight	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	27666520
MGI:5449045	M	MP:0004852	decreased testis weight	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0002662	abnormal cauda epididymis morphology	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	27666520
MGI:5449045	M	MP:0005376	homeostasis/metabolism phenotype	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	Y	24371141
MGI:5449045	M	MP:0003205	testicular atrophy	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0002687	oligozoospermia	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	27666520
MGI:5449045	M	MP:0002687	oligozoospermia	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0004901	decreased male germ cell number	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0014052	increased male germ cell apoptosis	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0002216	abnormal seminiferous tubule morphology	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	27666520
MGI:5449045	M	MP:0002216	abnormal seminiferous tubule morphology	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0008489	slow postnatal weight gain	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	27666520
MGI:5449045	M	MP:0014052	increased male germ cell apoptosis	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	27666520
MGI:5449045	M	MP:0020362	abnormal male germ cell physiology	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449045	M	MP:0001925	male infertility	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24371141
MGI:5449568	M	MP:0011091	prenatal lethality, complete penetrance	Ym/Y	involves: 101 * C3H	N	MGI:61668
MGI:5449570	F	MP:0010771	integument phenotype	Ym/Ym<+>	involves: 101 * C3H	Y	MGI:61668
MGI:5449570	F	MP:0000421	mottled coat	Ym/Ym<+>	involves: 101 * C3H	N	MGI:61668
MGI:5449570	F	MP:0001510	abnormal coat appearance	Ym/Ym<+>	involves: 101 * C3H	N	MGI:61668
MGI:5449629	F	MP:0003631	nervous system phenotype	Kiss1<tm1.1(cre/EGFP)Stei>/Kiss1<+>	involves: 129S6/SvEvTac * C57BL/6NCr	Y	21933870
MGI:5449730	M	MP:0010080	abnormal hepatocyte physiology	Tcf7l2<tm1a(EUCOMM)Wtsi>/Tcf7l2<+>	C57BL/6-Tcf7l2<tm1a(EUCOMM)Wtsi>	N	23028378
MGI:5449730	M	MP:0005293	impaired glucose tolerance	Tcf7l2<tm1a(EUCOMM)Wtsi>/Tcf7l2<+>	C57BL/6-Tcf7l2<tm1a(EUCOMM)Wtsi>	N	23028378
MGI:5449730	M	MP:0005559	increased circulating glucose level	Tcf7l2<tm1a(EUCOMM)Wtsi>/Tcf7l2<+>	C57BL/6-Tcf7l2<tm1a(EUCOMM)Wtsi>	N	23028378
MGI:5449730	M	MP:0002078	abnormal glucose homeostasis	Tcf7l2<tm1a(EUCOMM)Wtsi>/Tcf7l2<+>	C57BL/6-Tcf7l2<tm1a(EUCOMM)Wtsi>	N	23028378
MGI:5449730	M	MP:0003638	abnormal response/metabolism to endogenous compounds	Tcf7l2<tm1a(EUCOMM)Wtsi>/Tcf7l2<+>	C57BL/6-Tcf7l2<tm1a(EUCOMM)Wtsi>	N	23028378
MGI:5449976	M	MP:0000186	decreased circulating HDL cholesterol level	Baz1b<tm2a(KOMP)Wtsi>/Baz1b<+>	Not Specified	N	MGI:4839251
MGI:5449976	M	MP:0005567	decreased circulating total protein level	Baz1b<tm2a(KOMP)Wtsi>/Baz1b<+>	Not Specified	N	MGI:4839251
MGI:5449976	M	MP:0005179	decreased circulating cholesterol level	Baz1b<tm2a(KOMP)Wtsi>/Baz1b<+>	Not Specified	N	MGI:4839251
MGI:5449983	M	MP:0008501	increased IgG2b level	Mysm1<tm1a(KOMP)Wtsi>/Mysm1<tm1a(KOMP)Wtsi>	Not Specified	N	MGI:4839251
MGI:5449983	F	MP:0001512	trunk curl	Mysm1<tm1a(KOMP)Wtsi>/Mysm1<tm1a(KOMP)Wtsi>	Not Specified	N	MGI:4839251
MGI:5449983	F	MP:0005017	decreased B cell number	Mysm1<tm1a(KOMP)Wtsi>/Mysm1<tm1a(KOMP)Wtsi>	Not Specified	N	MGI:4839251
MGI:5449983	F	MP:0000322	increased granulocyte number	Mysm1<tm1a(KOMP)Wtsi>/Mysm1<tm1a(KOMP)Wtsi>	Not Specified	N	MGI:4839251
MGI:5449983	F	MP:0008211	decreased mature B cell number	Mysm1<tm1a(KOMP)Wtsi>/Mysm1<tm1a(KOMP)Wtsi>	Not Specified	N	MGI:4839251
MGI:5449983	M	MP:0000556	abnormal hindlimb morphology	Mysm1<tm1a(KOMP)Wtsi>/Mysm1<tm1a(KOMP)Wtsi>	Not Specified	N	MGI:4839251
MGI:5449983	F	MP:0005015	increased T cell number	Mysm1<tm1a(KOMP)Wtsi>/Mysm1<tm1a(KOMP)Wtsi>	Not Specified	N	MGI:4839251
MGI:5449983	M	MP:0000572	abnormal autopod morphology	Mysm1<tm1a(KOMP)Wtsi>/Mysm1<tm1a(KOMP)Wtsi>	Not Specified	N	MGI:4839251
MGI:5449983	M	MP:0001566	increased circulating phosphate level	Mysm1<tm1a(KOMP)Wtsi>/Mysm1<tm1a(KOMP)Wtsi>	Not Specified	N	MGI:4839251
MGI:5449985	M	MP:0002644	decreased circulating triglyceride level	Mysm1<tm1a(KOMP)Wtsi>/Mysm1<+>	Not Specified	N	MGI:4839251
MGI:5449985	M	MP:0002590	increased mean corpuscular volume	Mysm1<tm1a(KOMP)Wtsi>/Mysm1<+>	Not Specified	N	MGI:4839251
MGI:5450098	F	MP:0002896	abnormal bone mineralization	Cyb561<tm1a(EUCOMM)Wtsi>/Cyb561<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450098	F	MP:0008810	increased circulating iron level	Cyb561<tm1a(EUCOMM)Wtsi>/Cyb561<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450098	M	MP:0001413	abnormal response to new environment	Cyb561<tm1a(EUCOMM)Wtsi>/Cyb561<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450098	M	MP:0000195	decreased circulating calcium level	Cyb561<tm1a(EUCOMM)Wtsi>/Cyb561<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450098	F	MP:0006241	abnormal placement of pupils	Cyb561<tm1a(EUCOMM)Wtsi>/Cyb561<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450473	F	MP:0005316	abnormal response to tactile stimuli	Abcd4<tm1a(EUCOMM)Hmgu>/Abcd4<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5450473	F	MP:0001413	abnormal response to new environment	Abcd4<tm1a(EUCOMM)Hmgu>/Abcd4<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5450479	M	MP:0002966	decreased circulating alkaline phosphatase level	Aldh2<tm1a(EUCOMM)Wtsi>/Aldh2<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450479	M	MP:0005179	decreased circulating cholesterol level	Aldh2<tm1a(EUCOMM)Wtsi>/Aldh2<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450479	M	MP:0000183	decreased circulating LDL cholesterol level	Aldh2<tm1a(EUCOMM)Wtsi>/Aldh2<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450479	M	MP:0005567	decreased circulating total protein level	Aldh2<tm1a(EUCOMM)Wtsi>/Aldh2<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450479	M	MP:0000186	decreased circulating HDL cholesterol level	Aldh2<tm1a(EUCOMM)Wtsi>/Aldh2<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450496	F	MP:0000367	abnormal coat/ hair morphology	Brd7<tm2a(EUCOMM)Wtsi>/Brd7<+>	Not Specified	N	MGI:5285081
MGI:5450496	M	MP:0000745	tremors	Brd7<tm2a(EUCOMM)Wtsi>/Brd7<+>	Not Specified	N	MGI:4839251
MGI:5450519	F	MP:0000063	decreased bone mineral density	Cul7<tm1a(EUCOMM)Wtsi>/Cul7<+>	Not Specified	N	MGI:4839251
MGI:5450519	F	MP:0002896	abnormal bone mineralization	Cul7<tm1a(EUCOMM)Wtsi>/Cul7<+>	Not Specified	N	MGI:4839251
MGI:5450543	F	MP:0001262	decreased body weight	Mindy1<tm1a(EUCOMM)Wtsi>/Mindy1<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450543	F	MP:0002702	decreased circulating free fatty acids level	Mindy1<tm1a(EUCOMM)Wtsi>/Mindy1<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450543	F	MP:0003442	decreased circulating glycerol level	Mindy1<tm1a(EUCOMM)Wtsi>/Mindy1<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450546	F	MP:0003131	increased erythrocyte cell number	Fam83g<tm1a(EUCOMM)Wtsi>/Fam83g<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450546	M	MP:0002644	decreased circulating triglyceride level	Fam83g<tm1a(EUCOMM)Wtsi>/Fam83g<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450563	M	MP:0002644	decreased circulating triglyceride level	Grin2d<tm1a(EUCOMM)Wtsi>/Grin2d<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450608	M	MP:0002590	increased mean corpuscular volume	Nipsnap1<tm1a(EUCOMM)Wtsi>/Nipsnap1<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450608	F	MP:0003313	abnormal locomotor activation	Nipsnap1<tm1a(EUCOMM)Wtsi>/Nipsnap1<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450637	F	MP:0002966	decreased circulating alkaline phosphatase level	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5450641	M	MP:0002644	decreased circulating triglyceride level	Rnf7<tm1a(EUCOMM)Wtsi>/Rnf7<+>	Not Specified	N	MGI:4839251
MGI:5450641	F	MP:0005316	abnormal response to tactile stimuli	Rnf7<tm1a(EUCOMM)Wtsi>/Rnf7<+>	Not Specified	N	MGI:4839251
MGI:5450641	M	MP:0003019	increased circulating chloride level	Rnf7<tm1a(EUCOMM)Wtsi>/Rnf7<+>	Not Specified	N	MGI:4839251
MGI:5450641	F	MP:0003020	decreased circulating chloride level	Rnf7<tm1a(EUCOMM)Wtsi>/Rnf7<+>	Not Specified	N	MGI:4839251
MGI:5450701	M	MP:0002896	abnormal bone mineralization	Xylb<tm1a(EUCOMM)Hmgu>/Xylb<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5450701	M	MP:0001486	abnormal startle reflex	Xylb<tm1a(EUCOMM)Hmgu>/Xylb<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5450701	M	MP:0003960	increased lean body mass	Xylb<tm1a(EUCOMM)Hmgu>/Xylb<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5450701	M	MP:0000062	increased bone mineral density	Xylb<tm1a(EUCOMM)Hmgu>/Xylb<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5450706	M	MP:0002644	decreased circulating triglyceride level	Zfp704<tm1a(EUCOMM)Wtsi>/Zfp704<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5450849	M	MP:0001922	reduced male fertility	Gdf5<bp-4J>/Gdf5<bp-4J>	B6.Cg-Gdf5<bp-4J>/GrsrJ	N	MGI:5450727
MGI:5450864	M	MP:0002080	prenatal lethality	Muth1/Y	involves: 101/H * C3H/HeH	N	MGI:4940633
MGI:5450867	F	MP:0000414	alopecia	Muth1/Muth1<+>	involves: 101/H * C3H/HeH	N	MGI:4940633
MGI:5450867	F	MP:0011101	prenatal lethality, incomplete penetrance	Muth1/Muth1<+>	involves: 101/H * C3H/HeH	N	MGI:4940633
MGI:5450875	M	MP:0002111	abnormal tail morphology	Eda<Ta-36H>/Y	involves: 101/H * C3H/HeH	N	MGI:4940633
MGI:5461308	M	MP:0001745	increased circulating corticosterone level	Men1<tm1Rvt>/Men1<+>	involves: 129 * C57BL/6	N	19620250
MGI:5461497	M	MP:0005389	reproductive system phenotype	Gadd45g<tm1Jni>/Gadd45g<+>,X/Sry<AKR/J>,Tg(Map3k4)#Agre/0	involves: 129P2/OlaHsd * AKR/J * C57BL/6J	Y	23102580
MGI:5461561	M	MP:0001745	increased circulating corticosterone level	Gtf2ird1<Tg(Alb1-Myc)166.8Sst>/Gtf2ird1<Tg(Alb1-Myc)166.8Sst>	involves: C57BL/6J * CBA/J	N	22652393
MGI:5461561	M	MP:0010166	increased response to stress-induced hyperthermia	Gtf2ird1<Tg(Alb1-Myc)166.8Sst>/Gtf2ird1<Tg(Alb1-Myc)166.8Sst>	involves: C57BL/6J * CBA/J	N	22652393
MGI:5461561	M	MP:0001406	abnormal gait	Gtf2ird1<Tg(Alb1-Myc)166.8Sst>/Gtf2ird1<Tg(Alb1-Myc)166.8Sst>	involves: C57BL/6J * CBA/J	N	22652393
MGI:5461561	M	MP:0008489	slow postnatal weight gain	Gtf2ird1<Tg(Alb1-Myc)166.8Sst>/Gtf2ird1<Tg(Alb1-Myc)166.8Sst>	involves: C57BL/6J * CBA/J	N	22652393
MGI:5461561	M	MP:0001262	decreased body weight	Gtf2ird1<Tg(Alb1-Myc)166.8Sst>/Gtf2ird1<Tg(Alb1-Myc)166.8Sst>	involves: C57BL/6J * CBA/J	N	22652393
MGI:5461563	M	MP:0001262	decreased body weight	Gtf2ird1<Tg(Alb1-Myc)166.8Sst>/Gtf2ird1<+>	involves: C57BL/6J * CBA/J	N	22652393
MGI:5461563	M	MP:0008489	slow postnatal weight gain	Gtf2ird1<Tg(Alb1-Myc)166.8Sst>/Gtf2ird1<+>	involves: C57BL/6J * CBA/J	N	22652393
MGI:5461579	M	MP:0003921	abnormal heart left ventricle morphology	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0005608	cardiac interstitial fibrosis	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0003141	cardiac fibrosis	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0010546	abnormal subendocardium layer morphology	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0010511	shortened PR interval	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0001636	irregular heartbeat	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0010392	prolonged QRS complex duration	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0004070	abnormal P wave	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0010633	myocardium hypertrophy	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0004071	prolonged P wave	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0005329	abnormal myocardium layer morphology	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0004564	increased myocardial fiber size	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0002843	decreased systemic arterial blood pressure	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0003393	decreased cardiac output	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0005140	decreased cardiac muscle contractility	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461579	M	MP:0004485	increased response of heart to induced stress	Tg(Myh6-Erbb2)6Kaga/0	involves: C57BL/6J * SJL/J	N	22912742
MGI:5461824	M	MP:0003998	decreased thermal nociceptive threshold	Frmpd4<tm1.1Pfw>/Frmpd4<tm1.1Pfw>	B6.Cg-Frmpd4<tm1.1Pfw>	N	22561452
MGI:5461824	M	MP:0002736	abnormal nociception after inflammation	Frmpd4<tm1.1Pfw>/Frmpd4<tm1.1Pfw>	B6.Cg-Frmpd4<tm1.1Pfw>	N	22561452
MGI:5461824	M	MP:0002882	abnormal neuron morphology	Frmpd4<tm1.1Pfw>/Frmpd4<tm1.1Pfw>	B6.Cg-Frmpd4<tm1.1Pfw>	N	22561452
MGI:5461825	M	MP:0002736	abnormal nociception after inflammation	Homer2<tm1Mhd>/Homer2<tm1Mhd>,Homer3<tm1Mhd>/Homer3<tm1Mhd>	involves: 129S1/Sv * 129X1/SvJ	N	22561452
MGI:5461826	M	MP:0002736	abnormal nociception after inflammation	Grm5<tm1.1Kksz>/Grm5<tm1.1Kksz>	involves: 129S1/Sv * 129X1/SvJ	N	22561452
MGI:5461827	M	MP:0002736	abnormal nociception after inflammation	Homer1<tm2Mhd>/Homer1<tm2Mhd>	involves: 129S1/Sv * 129X1/SvJ	N	22561452
MGI:5462060	M	MP:0006362	abnormal male germ cell morphology	Nodal<tm1.1Ysa>/Nodal<tm1.1Ysa>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	23221368
MGI:5462061	M	MP:0005169	abnormal male meiosis	Smad4<tm2.1Cxd>/Smad4<tm2.1Cxd>,Tg(Dppa3-cre/Esr1*)3Sait/0	involves: 129S6/SvEvTac * C57BL/6 * DBA	N	23221368
MGI:5462366	M	MP:0009142	decreased prepulse inhibition	Tg(GFAP-tTA)6Hyms/0,Tg(tetO-HMOX1)6Hyms/0	involves: FVB/N	N	22875919
MGI:5463438	F	MP:0001463	abnormal spatial learning	Tg(Thy1-APPArc)M8Cagr/0	involves: C57BL/6 * CBA	N	19329229
MGI:5463438	F	MP:0008432	abnormal long-term spatial reference memory	Tg(Thy1-APPArc)M8Cagr/0	involves: C57BL/6 * CBA	N	19329229
MGI:5463446	F	MP:0011644	abnormal oviduct epithelium motile cilium morphology	Kif19a<tm1Noh>/Kif19a<tm1Noh>	involves: 129S6/SvEvTac * C57BL/6J	N	23168168
MGI:5463446	F	MP:0001926	female infertility	Kif19a<tm1Noh>/Kif19a<tm1Noh>	involves: 129S6/SvEvTac * C57BL/6J	N	23168168
MGI:5463446	F	MP:0003574	abnormal oviduct morphology	Kif19a<tm1Noh>/Kif19a<tm1Noh>	involves: 129S6/SvEvTac * C57BL/6J	N	23168168
MGI:5463446	F	MP:0003699	abnormal female reproductive system physiology	Kif19a<tm1Noh>/Kif19a<tm1Noh>	involves: 129S6/SvEvTac * C57BL/6J	N	23168168
MGI:5463448	F	MP:0011644	abnormal oviduct epithelium motile cilium morphology	Kif19a<tm1Noh>/Kif19a<+>	involves: 129S6/SvEvTac * C57BL/6J	N	23168168
MGI:5465167	M	MP:0004179	transmission ratio distortion	t<low2H>/t<+>	Not Specified	N	3653686
MGI:5465170	M	MP:0005389	reproductive system phenotype	t<h7m>/t<+>	Not Specified	Y	8690273
MGI:5465171	M	MP:0004179	transmission ratio distortion	t<h7m2>/t<+>	Not Specified	N	8690273
MGI:5465279	M	MP:0001925	male infertility	Slc9a8<Gt(YHB273)Byg>/Slc9a8<Gt(YHB273)Byg>	involves: 129P2/OlaHsd * Black Swiss	N	22575219
MGI:5465282	M	MP:0008911	induced hyperactivity	Srgap3<tm1.1Zi>/Srgap3<tm1.1Zi>	B6.129(SJL)-Srgap3<tm1.1Zi>	N	22820399
MGI:5465282	M	MP:0002780	decreased circulating testosterone level	Srgap3<tm1.1Zi>/Srgap3<tm1.1Zi>	B6.129(SJL)-Srgap3<tm1.1Zi>	N	22820399
MGI:5465282	F	MP:0009142	decreased prepulse inhibition	Srgap3<tm1.1Zi>/Srgap3<tm1.1Zi>	B6.129(SJL)-Srgap3<tm1.1Zi>	N	22820399
MGI:5465304	F	MP:0001935	decreased litter size	Fzd1<tm1.1Boer>/Fzd1<tm1.1Boer>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22954793
MGI:5465304	F	MP:0001127	small ovary	Fzd1<tm1.1Boer>/Fzd1<tm1.1Boer>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22954793
MGI:5465304	F	MP:0001132	absent mature ovarian follicles	Fzd1<tm1.1Boer>/Fzd1<tm1.1Boer>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22954793
MGI:5465304	F	MP:0009094	abnormal endometrial gland morphology	Fzd1<tm1.1Boer>/Fzd1<tm1.1Boer>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22954793
MGI:5465304	F	MP:0001126	abnormal ovary morphology	Fzd1<tm1.1Boer>/Fzd1<tm1.1Boer>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22954793
MGI:5465304	F	MP:0009096	decreased endometrial gland number	Fzd1<tm1.1Boer>/Fzd1<tm1.1Boer>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22954793
MGI:5465304	F	MP:0001923	reduced female fertility	Fzd1<tm1.1Boer>/Fzd1<tm1.1Boer>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22954793
MGI:5465304	F	MP:0001926	female infertility	Fzd1<tm1.1Boer>/Fzd1<tm1.1Boer>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22954793
MGI:5465304	F	MP:0001120	abnormal uterus morphology	Fzd1<tm1.1Boer>/Fzd1<tm1.1Boer>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22954793
MGI:5465400	M	MP:0002644	decreased circulating triglyceride level	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0005289	increased oxygen consumption	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0004889	increased energy expenditure	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0005659	decreased susceptibility to diet-induced obesity	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0001399	hyperactivity	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0002078	abnormal glucose homeostasis	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0005179	decreased circulating cholesterol level	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0008963	increased carbon dioxide production	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0010025	decreased total body fat amount	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0010378	increased respiratory quotient	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0011941	increased fluid intake	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0009125	decreased brown fat cell lipid droplet size	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0001433	polyphagia	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0002891	increased insulin sensitivity	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0002727	decreased circulating insulin level	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465400	M	MP:0005560	decreased circulating glucose level	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	22992738
MGI:5465401	M	MP:0008963	increased carbon dioxide production	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	B6.129P2-Mark4<Gt(XG191)Byg>	N	22992738
MGI:5465401	M	MP:0010378	increased respiratory quotient	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	B6.129P2-Mark4<Gt(XG191)Byg>	N	22992738
MGI:5465401	M	MP:0010025	decreased total body fat amount	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	B6.129P2-Mark4<Gt(XG191)Byg>	N	22992738
MGI:5465401	M	MP:0005289	increased oxygen consumption	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	B6.129P2-Mark4<Gt(XG191)Byg>	N	22992738
MGI:5465401	M	MP:0005659	decreased susceptibility to diet-induced obesity	Mark4<Gt(XG191)Byg>/Mark4<Gt(XG191)Byg>	B6.129P2-Mark4<Gt(XG191)Byg>	N	22992738
MGI:5465428	F	MP:0010024	increased total body fat amount	Esr1<tm4.2Ksk>/Esr1<tm4.2Ksk>	involves: C57BL/6 * C57BL/6NTac * CBA	N	20667977
MGI:5465428	M	MP:0005378	growth/size/body region phenotype	Esr1<tm4.2Ksk>/Esr1<tm4.2Ksk>	involves: C57BL/6 * C57BL/6NTac * CBA	Y	20667977
MGI:5465428	F	MP:0003572	abnormal uterus development	Esr1<tm4.2Ksk>/Esr1<tm4.2Ksk>	involves: C57BL/6 * C57BL/6NTac * CBA	N	20667977
MGI:5465428	F	MP:0000062	increased bone mineral density	Esr1<tm4.2Ksk>/Esr1<tm4.2Ksk>	involves: C57BL/6 * C57BL/6NTac * CBA	N	20667977
MGI:5465428	F	MP:0001751	increased circulating luteinizing hormone level	Esr1<tm4.2Ksk>/Esr1<tm4.2Ksk>	involves: C57BL/6 * C57BL/6NTac * CBA	N	20667977
MGI:5465428	F	MP:0002865	increased growth rate	Esr1<tm4.2Ksk>/Esr1<tm4.2Ksk>	involves: C57BL/6 * C57BL/6NTac * CBA	N	20667977
MGI:5465428	F	MP:0000628	abnormal mammary gland development	Esr1<tm4.2Ksk>/Esr1<tm4.2Ksk>	involves: C57BL/6 * C57BL/6NTac * CBA	N	20667977
MGI:5465428	F	MP:0001260	increased body weight	Esr1<tm4.2Ksk>/Esr1<tm4.2Ksk>	involves: C57BL/6 * C57BL/6NTac * CBA	N	20667977
MGI:5465428	F	MP:0002781	increased circulating testosterone level	Esr1<tm4.2Ksk>/Esr1<tm4.2Ksk>	involves: C57BL/6 * C57BL/6NTac * CBA	N	20667977
MGI:5465442	F	MP:0005289	increased oxygen consumption	Ifitm1<tm1.1Ieg>/Ifitm1<tm1.1Ieg>	B6.129P2-Ifitm1<tm1.1Ieg>	N	23115618
MGI:5465442	F	MP:0002665	decreased circulating corticosterone level	Ifitm1<tm1.1Ieg>/Ifitm1<tm1.1Ieg>	B6.129P2-Ifitm1<tm1.1Ieg>	N	23115618
MGI:5465442	M	MP:0005180	abnormal circulating testosterone level	Ifitm1<tm1.1Ieg>/Ifitm1<tm1.1Ieg>	B6.129P2-Ifitm1<tm1.1Ieg>	N	23115618
MGI:5465463	M	MP:0001925	male infertility	Gatm<tm1.1Isb>/Gatm<tm1.1Isb>	B6.129-Gatm<tm1.1Isb>	N	23026748
MGI:5465463	F	MP:0001926	female infertility	Gatm<tm1.1Isb>/Gatm<tm1.1Isb>	B6.129-Gatm<tm1.1Isb>	N	23026748
MGI:5465463	M	MP:0001156	abnormal spermatogenesis	Gatm<tm1.1Isb>/Gatm<tm1.1Isb>	B6.129-Gatm<tm1.1Isb>	N	23026748
MGI:5465463	M	MP:0001146	abnormal testis morphology	Gatm<tm1.1Isb>/Gatm<tm1.1Isb>	B6.129-Gatm<tm1.1Isb>	N	23026748
MGI:5466292	M	MP:0002727	decreased circulating insulin level	Tbc1d4<tm1Lex>/Tbc1d4<tm1Lex>	involves: 129S/SvEvBrd * C57BL/6J * C57BL/6N	N	23011063
MGI:5466292	F	MP:0005293	impaired glucose tolerance	Tbc1d4<tm1Lex>/Tbc1d4<tm1Lex>	involves: 129S/SvEvBrd * C57BL/6J * C57BL/6N	N	23011063
MGI:5466357	F	MP:0009504	abnormal mammary gland epithelium morphology	Cebpd<tm1Pfj>/Cebpd<tm1Pfj>	involves: 129S1/Sv	N	12626772
MGI:5466357	F	MP:0000662	abnormal branching of the mammary ductal tree	Cebpd<tm1Pfj>/Cebpd<tm1Pfj>	involves: 129S1/Sv	N	12626772
MGI:5466357	F	MP:0010173	increased mammary gland epithelial cell proliferation	Cebpd<tm1Pfj>/Cebpd<tm1Pfj>	involves: 129S1/Sv	N	12626772
MGI:5466370	M	MP:0002687	oligozoospermia	Selenop<tm3.1Rfb>/Selenop<tm3.1Rfb>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * DBA	N	23038251
MGI:5466370	M	MP:0005578	teratozoospermia	Selenop<tm3.1Rfb>/Selenop<tm3.1Rfb>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * DBA	N	23038251
MGI:5466414	F	MP:0001385	pup cannibalization	Tg(Nes-cre)1Kln/0,Zfp568<tm1Ckjs>/Zfp568<tm1Ckjs>	involves: C57BL/6J * SJL	N	23071813
MGI:5466536	F	MP:0005016	decreased lymphocyte cell number	Mcat<tm1.1Ssmi>/Mcat<tm1.1Ssmi>,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA	N	23077570
MGI:5466536	F	MP:0000221	decreased leukocyte cell number	Mcat<tm1.1Ssmi>/Mcat<tm1.1Ssmi>,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA	N	23077570
MGI:5466572	M	MP:0001147	small testis	Hormad2<tm1Kura>/Hormad2<tm1Kura>	either: B6.Cg-Hormad2<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	23039116
MGI:5466572	M	MP:0001925	male infertility	Hormad2<tm1Kura>/Hormad2<tm1Kura>	either: B6.Cg-Hormad2<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	23039116
MGI:5466572	F	MP:0005389	reproductive system phenotype	Hormad2<tm1Kura>/Hormad2<tm1Kura>	either: B6.Cg-Hormad2<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	Y	23039116
MGI:5466572	F	MP:0005168	abnormal female meiosis	Hormad2<tm1Kura>/Hormad2<tm1Kura>	either: B6.Cg-Hormad2<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	23039116
MGI:5466572	M	MP:0005159	azoospermia	Hormad2<tm1Kura>/Hormad2<tm1Kura>	either: B6.Cg-Hormad2<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	23039116
MGI:5466572	M	MP:0005169	abnormal male meiosis	Hormad2<tm1Kura>/Hormad2<tm1Kura>	either: B6.Cg-Hormad2<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	23039116
MGI:5466572	M	MP:0004852	decreased testis weight	Hormad2<tm1Kura>/Hormad2<tm1Kura>	either: B6.Cg-Hormad2<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	23039116
MGI:5466572	M	MP:0008280	abnormal male germ cell apoptosis	Hormad2<tm1Kura>/Hormad2<tm1Kura>	either: B6.Cg-Hormad2<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	23039116
MGI:5466573	F	MP:0005168	abnormal female meiosis	Hormad2<tm1Kura>/Hormad2<+>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	23039116
MGI:5466573	F	MP:0005431	decreased oocyte number	Hormad2<tm1Kura>/Hormad2<+>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	23039116
MGI:5466573	F	MP:0005389	reproductive system phenotype	Hormad2<tm1Kura>/Hormad2<+>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	Y	23039116
MGI:5466574	F	MP:0005389	reproductive system phenotype	Hormad2<tm1Kura>/Hormad2<tm1Kura>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	Y	23039116
MGI:5466574	F	MP:0005168	abnormal female meiosis	Hormad2<tm1Kura>/Hormad2<tm1Kura>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	23039116
MGI:5466574	M	MP:0001146	abnormal testis morphology	Hormad2<tm1Kura>/Hormad2<tm1Kura>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	23039116
MGI:5466678	M	MP:0004852	decreased testis weight	Bmyc<tm1Mpo>/Bmyc<tm1Mpo>	involves: 129S7/SvEvBrd * C57BL/6N	N	22869780
MGI:5466678	M	MP:0014052	increased male germ cell apoptosis	Bmyc<tm1Mpo>/Bmyc<tm1Mpo>	involves: 129S7/SvEvBrd * C57BL/6N	N	22869780
MGI:5466678	M	MP:0001751	increased circulating luteinizing hormone level	Bmyc<tm1Mpo>/Bmyc<tm1Mpo>	involves: 129S7/SvEvBrd * C57BL/6N	N	22869780
MGI:5466678	M	MP:0001262	decreased body weight	Bmyc<tm1Mpo>/Bmyc<tm1Mpo>	involves: 129S7/SvEvBrd * C57BL/6N	N	22869780
MGI:5466678	M	MP:0009248	small caput epididymis	Bmyc<tm1Mpo>/Bmyc<tm1Mpo>	involves: 129S7/SvEvBrd * C57BL/6N	N	22869780
MGI:5466678	M	MP:0004929	decreased epididymis weight	Bmyc<tm1Mpo>/Bmyc<tm1Mpo>	involves: 129S7/SvEvBrd * C57BL/6N	N	22869780
MGI:5466678	M	MP:0002006	neoplasm	Bmyc<tm1Mpo>/Bmyc<tm1Mpo>	involves: 129S7/SvEvBrd * C57BL/6N	Y	22869780
MGI:5466678	M	MP:0011385	abnormal testosterone level	Bmyc<tm1Mpo>/Bmyc<tm1Mpo>	involves: 129S7/SvEvBrd * C57BL/6N	N	22869780
MGI:5466678	M	MP:0001154	seminiferous tubule degeneration	Bmyc<tm1Mpo>/Bmyc<tm1Mpo>	involves: 129S7/SvEvBrd * C57BL/6N	N	22869780
MGI:5466878	F	MP:0002644	decreased circulating triglyceride level	Ttc39b<tm1e(EUCOMM)Wtsi>/Ttc39b<+>	Not Specified	N	MGI:4839251
MGI:5467304	M	MP:0001167	prostate gland epithelial hyperplasia	Spry1<tm1Jdli>/Spry1<tm1.1Jdli>,Spry2<tm1Mrt>/Spry2<tm1.1Mrt>,Tg(Osr1-cre)4Mrt/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * FVB/N	N	23150596
MGI:5467304	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Spry1<tm1Jdli>/Spry1<tm1.1Jdli>,Spry2<tm1Mrt>/Spry2<tm1.1Mrt>,Tg(Osr1-cre)4Mrt/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * FVB/N	N	23150596
MGI:5467305	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm2.1Ppp>/Pten<+>,Spry1<tm1Jdli>/Spry1<tm1.1Jdli>,Spry2<tm1Mrt>/Spry2<tm1.1Mrt>,Tg(Osr1-cre)4Mrt/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * FVB/N	N	23150596
MGI:5467305	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm2.1Ppp>/Pten<+>,Spry1<tm1Jdli>/Spry1<tm1.1Jdli>,Spry2<tm1Mrt>/Spry2<tm1.1Mrt>,Tg(Osr1-cre)4Mrt/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * FVB/N	N	23150596
MGI:5467306	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(CAG-Bgeo,-Spry2,-ALPP)1Mrt/0,Tg(Osr1-cre)4Mrt/0	involves: 129P2/OlaHsd * 129S1/Sv * FVB/N	N	23150596
MGI:5467307	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Osr1-cre)4Mrt/0	involves: 129S1/Sv * 129X1/SvJ	N	23150596
MGI:5467335	M	MP:0005389	reproductive system phenotype	Mamld1<tm1Tsga>/Y	involves: 129 * C57BL/6	Y	23087174
MGI:5467972	F	MP:0003718	maternal effect	Aldh2<tm1a(EUCOMM)Wtsi>/Aldh2<tm1a(EUCOMM)Wtsi>,Fancd2<tm1Hou>/Fancd2<+>	involves: 129S4/SvJae * C57BL/6J * C57BL/6N	N	21734703
MGI:5467989	M	MP:0001559	hyperglycemia	Rbm4<tm1Wtarn>/Rbm4<tm1Wtarn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23129807
MGI:5467989	M	MP:0005293	impaired glucose tolerance	Rbm4<tm1Wtarn>/Rbm4<tm1Wtarn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23129807
MGI:5467989	M	MP:0002078	abnormal glucose homeostasis	Rbm4<tm1Wtarn>/Rbm4<tm1Wtarn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23129807
MGI:5467989	M	MP:0002727	decreased circulating insulin level	Rbm4<tm1Wtarn>/Rbm4<tm1Wtarn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23129807
MGI:5467990	M	MP:0001559	hyperglycemia	Rbm4b<tm1Wtarn>/Rbm4b<tm1Wtarn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23129807
MGI:5467990	M	MP:0005293	impaired glucose tolerance	Rbm4b<tm1Wtarn>/Rbm4b<tm1Wtarn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23129807
MGI:5467997	F	MP:0021182	decreased femoral compact bone area	Wnt16<tm1Lex>/Wnt16<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	22792071
MGI:5468675	M	MP:0030884	rachitic rosary	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16585534
MGI:5468675	M	MP:0030679	decreased hydroxyproline level	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	19482009
MGI:5468675	M	MP:0005332	abnormal amino acid level	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16585534
MGI:5468675	M	MP:0000063	decreased bone mineral density	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16585534
MGI:5468675	M	MP:0010027	increased liver cholesterol level	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	14975739
MGI:5468675	M	MP:0002152	abnormal brain morphology	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16500693
MGI:5468675	M	MP:0003674	oxidative stress	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16728709
MGI:5468675	M	MP:0011229	abnormal vitamin C level	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16585534
MGI:5468675	M	MP:0011229	abnormal vitamin C level	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	19482009
MGI:5468675	M	MP:0003674	oxidative stress	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16500693
MGI:5468675	M	MP:0002655	abnormal keratinocyte morphology	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	19482009
MGI:5468675	M	MP:0030827	femur fracture	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16585534
MGI:5468675	M	MP:0005459	decreased percent body fat/body weight	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16585534
MGI:5468675	M	MP:0002628	hepatic steatosis	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	14975739
MGI:5468675	M	MP:0001958	emphysema	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16728709
MGI:5468675	M	MP:0004777	abnormal phospholipid level	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	14975739
MGI:5468675	M	MP:0000607	abnormal hepatocyte morphology	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	14975739
MGI:5468675	M	MP:0000427	abnormal hair cycle	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	19482009
MGI:5468675	M	MP:0009355	increased liver triglyceride level	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	14975739
MGI:5468675	M	MP:0008412	increased cellular sensitivity to oxidative stress	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16728709
MGI:5468675	M	MP:0005311	abnormal circulating amino acid level	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16585534
MGI:5468675	M	MP:0001406	abnormal gait	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16585534
MGI:5468675	M	MP:0010911	abnormal pulmonary acinus morphology	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16728709
MGI:5468675	M	MP:0005584	abnormal enzyme/coenzyme activity	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16585534
MGI:5468675	M	MP:0010911	abnormal pulmonary acinus morphology	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	14989739
MGI:5468675	M	MP:0001263	weight loss	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16728709
MGI:5468675	M	MP:0001263	weight loss	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16585534
MGI:5468675	M	MP:0001244	thin dermal layer	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	19482009
MGI:5468675	M	MP:0001262	decreased body weight	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	14975739
MGI:5468675	M	MP:0009820	abnormal liver vasculature morphology	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	14975739
MGI:5468675	M	MP:0002083	premature death	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	14975739
MGI:5468675	M	MP:0009763	increased susceptibility to induced morbidity/mortality	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd	N	16585534
MGI:5468721	F	MP:0020518	renal glomerular protein deposits	Fcgr2b<tm1Kgcs>/Fcgr2b<+>	involves: C57BL/6	N	23109709
MGI:5469203	M	MP:0000751	myopathy	Mtm1<Gt(OST290577)Lex>/Y	involves: 129S5/SvEvBrd * C57BL/6	N	23109424
MGI:5469203	M	MP:0001262	decreased body weight	Mtm1<Gt(OST290577)Lex>/Y	involves: 129S5/SvEvBrd * C57BL/6	N	23109424
MGI:5469203	M	MP:0004091	abnormal Z line morphology	Mtm1<Gt(OST290577)Lex>/Y	involves: 129S5/SvEvBrd * C57BL/6	N	23109424
MGI:5469203	M	MP:0003674	oxidative stress	Mtm1<Gt(OST290577)Lex>/Y	involves: 129S5/SvEvBrd * C57BL/6	N	23109424
MGI:5469203	M	MP:0009404	centrally nucleated skeletal muscle fibers	Mtm1<Gt(OST290577)Lex>/Y	involves: 129S5/SvEvBrd * C57BL/6	N	23109424
MGI:5469203	M	MP:0030940	impaired autophagy	Mtm1<Gt(OST290577)Lex>/Y	involves: 129S5/SvEvBrd * C57BL/6	N	23109424
MGI:5469203	M	MP:0004232	decreased muscle weight	Mtm1<Gt(OST290577)Lex>/Y	involves: 129S5/SvEvBrd * C57BL/6	N	23109424
MGI:5469203	M	MP:0006036	abnormal mitochondrial physiology	Mtm1<Gt(OST290577)Lex>/Y	involves: 129S5/SvEvBrd * C57BL/6	N	23109424
MGI:5469203	M	MP:0009400	decreased skeletal muscle fiber size	Mtm1<Gt(OST290577)Lex>/Y	involves: 129S5/SvEvBrd * C57BL/6	N	23109424
MGI:5469203	M	MP:0010053	decreased grip strength	Mtm1<Gt(OST290577)Lex>/Y	involves: 129S5/SvEvBrd * C57BL/6	N	23109424
MGI:5469310	M	MP:0005389	reproductive system phenotype	Piwil2<tm1Nkn>/Piwil2<tm1Nkn>,Tg(Piwil2)#Hsas/0	involves: 129S2/SvPas	Y	23132912
MGI:5469321	M	MP:0011229	abnormal vitamin C level	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd * C57BL/6	N	22155581
MGI:5469321	M	MP:0011229	abnormal vitamin C level	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19733551
MGI:5469321	M	MP:0002857	cochlear ganglion degeneration	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19733551
MGI:5469321	M	MP:0010252	anterior subcapsular cataract	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd * C57BL/6	N	22155581
MGI:5469321	M	MP:0011967	increased or absent threshold for auditory brainstem response	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19733551
MGI:5469321	M	MP:0000414	alopecia	Rgn<tm1Aish>/Y	involves: 129P2/OlaHsd * C57BL/6	N	19733551
MGI:5469394	M	MP:0009239	short sperm flagellum	Rabl2<mot>/Rabl2<mot>	involves: C57BL/6 * CBA	N	23055941
MGI:5469394	M	MP:0002675	asthenozoospermia	Rabl2<mot>/Rabl2<mot>	involves: C57BL/6 * CBA	N	23055941
MGI:5469394	M	MP:0004852	decreased testis weight	Rabl2<mot>/Rabl2<mot>	involves: C57BL/6 * CBA	N	23055941
MGI:5469394	M	MP:0002687	oligozoospermia	Rabl2<mot>/Rabl2<mot>	involves: C57BL/6 * CBA	N	23055941
MGI:5469394	M	MP:0001925	male infertility	Rabl2<mot>/Rabl2<mot>	involves: C57BL/6 * CBA	N	23055941
MGI:5469395	M	MP:0001925	male infertility	Rabl2<mot>/Rabl2<mot>	C57BL/6(CBA)-Rabl2<mot>	N	23055941
MGI:5469591	M	MP:0002006	neoplasm	Pik3ca<tm1Gne>/Pik3ca<+>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6N * FVB/N	Y	22370636
MGI:5469591	F	MP:0010299	increased mammary gland tumor incidence	Pik3ca<tm1Gne>/Pik3ca<+>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6N * FVB/N	N	22370636
MGI:5469591	F	MP:0000662	abnormal branching of the mammary ductal tree	Pik3ca<tm1Gne>/Pik3ca<+>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6N * FVB/N	N	22370636
MGI:5469886	M	MP:0005389	reproductive system phenotype	Mirc34<tm1.1Cxu>/Mirc34<tm1.1Cxu>	involves: 129S7/SvEvBrd * C57BL/6 * SJL	Y	22570483
MGI:5469887	M	MP:0005389	reproductive system phenotype	Mirc34<tm1.1Cxu>/Mirc34<tm1.1Cxu>	B6.129S7-Mirc34<tm1.1Cxu>	Y	22570483
MGI:5469888	M	MP:0005389	reproductive system phenotype	Mirc34<tm1.1Cxu>/Mirc34<tm1.1Cxu>	129S7(B6)-Mirc34<tm1.1Cxu>	Y	22570483
MGI:5470166	M	MP:0002169	no abnormal phenotype detected	Zic3<tm2.1Jwb>/Y	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J	N	23184148
MGI:5470167	F	MP:0002169	no abnormal phenotype detected	Zic3<tm2.1Jwb>/Zic3<tm2.1Jwb>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J	N	23184148
MGI:5470168	M	MP:0010808	right-sided stomach	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0006065	abnormal heart position or orientation	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0004252	abnormal direction of heart looping	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0006063	abnormal inferior vena cava morphology	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0000914	exencephaly	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0000269	abnormal heart looping	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0010402	ventricular septal defect	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0010403	atrial septal defect	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0003984	embryonic growth retardation	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0002151	abnormal neural tube morphology	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0000755	hindlimb paralysis	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0001672	abnormal embryo development	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0004133	heterotaxia	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0005034	abnormal anus morphology	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0000644	dextrocardia	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0000585	kinked tail	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0002114	abnormal axial skeleton morphology	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0002092	abnormal eye morphology	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0000111	cleft palate	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0010853	abnormal lung position or orientation	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470168	M	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance	Zic3<tm2.1Jwb>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA	N	23184148
MGI:5470169	M	MP:0002169	no abnormal phenotype detected	Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>,Zic3<tm2.1Jwb>/Y	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J	N	23184148
MGI:5470170	M	MP:0002169	no abnormal phenotype detected	Zic3<tm2.1Jwb>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J * CBA/J	N	23184148
MGI:5470171	M	MP:0002169	no abnormal phenotype detected	Mesp1<tm2(cre)Ysa>/Mesp1<+>,Zic3<tm2.1Jwb>/Y	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA/JNCrlj	N	23184148
MGI:5470172	M	MP:0000269	abnormal heart looping	Zic3<tm2.1Jwb>/Y,Tg(T-cre)1Lwd/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C3H * C57BL/6	N	23184148
MGI:5470172	M	MP:0004133	heterotaxia	Zic3<tm2.1Jwb>/Y,Tg(T-cre)1Lwd/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C3H * C57BL/6	N	23184148
MGI:5470172	M	MP:0011110	preweaning lethality, incomplete penetrance	Zic3<tm2.1Jwb>/Y,Tg(T-cre)1Lwd/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C3H * C57BL/6	N	23184148
MGI:5470172	M	MP:0000585	kinked tail	Zic3<tm2.1Jwb>/Y,Tg(T-cre)1Lwd/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C3H * C57BL/6	N	23184148
MGI:5471586	F	MP:0001860	liver inflammation	Insr<tm1Khn>/Insr<tm1Khn>,Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	N	23119079
MGI:5471586	F	MP:0005669	increased circulating leptin level	Insr<tm1Khn>/Insr<tm1Khn>,Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	N	23119079
MGI:5471586	F	MP:0001868	ovary inflammation	Insr<tm1Khn>/Insr<tm1Khn>,Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	N	23119079
MGI:5471586	F	MP:0005335	abnormal gonadal fat pad morphology	Insr<tm1Khn>/Insr<tm1Khn>,Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	N	23119079
MGI:5471586	F	MP:0003355	decreased ovulation rate	Insr<tm1Khn>/Insr<tm1Khn>,Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	N	23119079
MGI:5471586	F	MP:0001132	absent mature ovarian follicles	Insr<tm1Khn>/Insr<tm1Khn>,Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	N	23119079
MGI:5471586	F	MP:0001134	absent corpus luteum	Insr<tm1Khn>/Insr<tm1Khn>,Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	N	23119079
MGI:5471586	F	MP:0003961	decreased lean body mass	Insr<tm1Khn>/Insr<tm1Khn>,Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	N	23119079
MGI:5471586	F	MP:0031602	white adipose tissue inflammation	Insr<tm1Khn>/Insr<tm1Khn>,Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	N	23119079
MGI:5471586	F	MP:0001559	hyperglycemia	Insr<tm1Khn>/Insr<tm1Khn>,Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	N	23119079
MGI:5471586	F	MP:0020411	increased abdominal adipose tissue amount	Insr<tm1Khn>/Insr<tm1Khn>,Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	N	23119079
MGI:5471586	F	MP:0006094	increased fat cell size	Insr<tm1Khn>/Insr<tm1Khn>,Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	N	23119079
MGI:5471586	F	MP:0005458	increased percent body fat/body weight	Insr<tm1Khn>/Insr<tm1Khn>,Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	N	23119079
MGI:5471747	M	MP:0005378	growth/size/body region phenotype	Drd2<tm1.1Mrub>/Drd2<tm1.1Mrub>,Tg(Prl-cre)1Mrub/?	involves: 129S4/SvJae * C57BL/6 * CBA	Y	23536095
MGI:5471750	M	MP:0011532	decreased urine major urinary protein level	Drd2<tm1.1Mrub>/Drd2<tm1.1Mrub>,Tg(Nes-cre)1Kln/?	involves: 129S4/SvJae * C57BL/6 * SJL	N	23536095
MGI:5471750	M	MP:0001732	postnatal growth retardation	Drd2<tm1.1Mrub>/Drd2<tm1.1Mrub>,Tg(Nes-cre)1Kln/?	involves: 129S4/SvJae * C57BL/6 * SJL	N	23536095
MGI:5471750	M	MP:0008489	slow postnatal weight gain	Drd2<tm1.1Mrub>/Drd2<tm1.1Mrub>,Tg(Nes-cre)1Kln/?	involves: 129S4/SvJae * C57BL/6 * SJL	N	23536095
MGI:5471750	M	MP:0002557	abnormal social/conspecific interaction behavior	Drd2<tm1.1Mrub>/Drd2<tm1.1Mrub>,Tg(Nes-cre)1Kln/?	involves: 129S4/SvJae * C57BL/6 * SJL	N	23536095
MGI:5473342	M	MP:0005590	increased vasodilation	Ptgdr<tm1Dgen>/Ptgdr<+>	B6.129P2-Ptgdr<tm1Dgen>	N	16617107
MGI:5473526	M	MP:0011957	decreased compensatory feeding amount	Pomc<tm2Low>/Pomc<tm2Low>	B6.129S4-Pomc<tm2Low>	N	23093774
MGI:5473527	M	MP:0009285	increased gonadal fat pad weight	Pomc<tm2Low>/Pomc<tm2Low>,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129S4/SvJae * C57BL/6 * CBA	N	23093774
MGI:5473607	M	MP:0005189	abnormal anogenital distance	Frem1<eyes2>/Frem1<eyes2>	C57BL/6J-Frem1<eyes2>	N	23536828
MGI:5473900	M	MP:0002216	abnormal seminiferous tubule morphology	Alkbh5<tm1.1Klng>/Alkbh5<tm1.1Klng>	Not Specified	N	23177736
MGI:5473900	M	MP:0004852	decreased testis weight	Alkbh5<tm1.1Klng>/Alkbh5<tm1.1Klng>	Not Specified	N	23177736
MGI:5473900	M	MP:0001147	small testis	Alkbh5<tm1.1Klng>/Alkbh5<tm1.1Klng>	Not Specified	N	23177736
MGI:5473900	M	MP:0001922	reduced male fertility	Alkbh5<tm1.1Klng>/Alkbh5<tm1.1Klng>	Not Specified	N	23177736
MGI:5473900	M	MP:0008280	abnormal male germ cell apoptosis	Alkbh5<tm1.1Klng>/Alkbh5<tm1.1Klng>	Not Specified	N	23177736
MGI:5473900	M	MP:0005578	teratozoospermia	Alkbh5<tm1.1Klng>/Alkbh5<tm1.1Klng>	Not Specified	N	23177736
MGI:5473900	M	MP:0002687	oligozoospermia	Alkbh5<tm1.1Klng>/Alkbh5<tm1.1Klng>	Not Specified	N	23177736
MGI:5473976	M	MP:0001262	decreased body weight	Ptp4a3<tm1.1Geh>/Ptp4a3<tm1.1Geh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23555575
MGI:5473976	M	MP:0006086	decreased body mass index	Ptp4a3<tm1.1Geh>/Ptp4a3<tm1.1Geh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23555575
MGI:5474008	M	MP:0010053	decreased grip strength	Cacna1s<tm1.1Cann>/Cacna1s<+>	involves: 129	N	23187123
MGI:5474203	F	MP:0004919	abnormal positive T cell selection	Cd3e<tm1.1Geno>/Cd3e<tm1.1Geno>,Tg(TcraH-Y,TcrbH-Y)71Vbo/0	involves: C57BL/6 * C57BL/6J * DBA/2J	N	23267019
MGI:5474203	M	MP:0004918	abnormal negative T cell selection	Cd3e<tm1.1Geno>/Cd3e<tm1.1Geno>,Tg(TcraH-Y,TcrbH-Y)71Vbo/0	involves: C57BL/6 * C57BL/6J * DBA/2J	N	23267019
MGI:5474382	M	MP:0001922	reduced male fertility	H3f3a<tm1.2Mnn>/H3f3a<tm1.2Mnn>	involves: 129S1/Sv * 129S1/SvImJ * 129S4/SvJaeSor	N	23315948
MGI:5474384	M	MP:0001925	male infertility	H3f3b<tm1.2Mnn>/H3f3b<+>	involves: 129S1/Sv * 129S1/SvImJ * 129S4/SvJaeSor	N	23315948
MGI:5474384	M	MP:0008279	arrest of spermiogenesis	H3f3b<tm1.2Mnn>/H3f3b<+>	involves: 129S1/Sv * 129S1/SvImJ * 129S4/SvJaeSor	N	23315948
MGI:5474573	F	MP:0001473	reduced long-term potentiation	Trpc5<tm1.1Lbi>/Trpc5<tm1.1Lbi>	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	23188715
MGI:5474573	F	MP:0005386	behavior/neurological phenotype	Trpc5<tm1.1Lbi>/Trpc5<tm1.1Lbi>	involves: 129S6/SvEvTac * C57BL/6 * CBA	Y	23188715
MGI:5474573	F	MP:0002887	decreased susceptibility to pharmacologically induced seizures	Trpc5<tm1.1Lbi>/Trpc5<tm1.1Lbi>	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	23188715
MGI:5474573	F	MP:0008236	decreased susceptibility to neuronal excitotoxicity	Trpc5<tm1.1Lbi>/Trpc5<tm1.1Lbi>	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	23188715
MGI:5474574	M	MP:0005386	behavior/neurological phenotype	Trpc5<tm1.1Lbi>/Y	involves: 129S6/SvEvTac * C57BL/6 * CBA	Y	23188715
MGI:5474574	M	MP:0002887	decreased susceptibility to pharmacologically induced seizures	Trpc5<tm1.1Lbi>/Y	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	23188715
MGI:5474574	M	MP:0008236	decreased susceptibility to neuronal excitotoxicity	Trpc5<tm1.1Lbi>/Y	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	23188715
MGI:5474574	M	MP:0001473	reduced long-term potentiation	Trpc5<tm1.1Lbi>/Y	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	23188715
MGI:5474635	F	MP:0003845	abnormal decidualization	Wnt6<tm1Akis>/Wnt6<tm1Akis>	involves: 129P2/OlaHsd * CD-1 * NMRI	N	23175771
MGI:5474635	F	MP:0003077	abnormal cell cycle	Wnt6<tm1Akis>/Wnt6<tm1Akis>	involves: 129P2/OlaHsd * CD-1 * NMRI	N	23175771
MGI:5474635	F	MP:0004256	abnormal maternal decidual layer morphology	Wnt6<tm1Akis>/Wnt6<tm1Akis>	involves: 129P2/OlaHsd * CD-1 * NMRI	N	23175771
MGI:5474635	F	MP:0001935	decreased litter size	Wnt6<tm1Akis>/Wnt6<tm1Akis>	involves: 129P2/OlaHsd * CD-1 * NMRI	N	23175771
MGI:5474635	F	MP:0001727	abnormal embryo implantation	Wnt6<tm1Akis>/Wnt6<tm1Akis>	involves: 129P2/OlaHsd * CD-1 * NMRI	N	23175771
MGI:5474635	F	MP:0000352	decreased cell proliferation	Wnt6<tm1Akis>/Wnt6<tm1Akis>	involves: 129P2/OlaHsd * CD-1 * NMRI	N	23175771
MGI:5474794	F	MP:0005389	reproductive system phenotype	Gt(ROSA)26Sor<tm1(CAG-NR2F1)Mjts>/Gt(ROSA)26Sor<+>,Nr2f2<tm2.1Tsa>/Nr2f2<tm2.1Tsa>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ	Y	20382891
MGI:5474795	F	MP:0001926	female infertility	Nr2f2<tm2.1Tsa>/Nr2f2<tm2.1Tsa>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ	N	20382891
MGI:5474842	M	MP:0009141	increased prepulse inhibition	Impa2<tm1.2Tohn>/Impa2<tm1.2Tohn>	involves: C57BL/6 * C57BL/6JJcl * C57BL/6NCrSlc	N	23205734
MGI:5474963	M	MP:0014171	increased fatty acid oxidation	Mfsd2a<tm1Dls>/Mfsd2a<tm1Dls>	B6.Cg-Mfsd2a<tm1Dls>	N	23209793
MGI:5474963	M	MP:0009133	decreased white fat cell size	Mfsd2a<tm1Dls>/Mfsd2a<tm1Dls>	B6.Cg-Mfsd2a<tm1Dls>	N	23209793
MGI:5474963	M	MP:0002644	decreased circulating triglyceride level	Mfsd2a<tm1Dls>/Mfsd2a<tm1Dls>	B6.Cg-Mfsd2a<tm1Dls>	N	23209793
MGI:5474963	M	MP:0010378	increased respiratory quotient	Mfsd2a<tm1Dls>/Mfsd2a<tm1Dls>	B6.Cg-Mfsd2a<tm1Dls>	N	23209793
MGI:5474963	M	MP:0005318	decreased triglyceride level	Mfsd2a<tm1Dls>/Mfsd2a<tm1Dls>	B6.Cg-Mfsd2a<tm1Dls>	N	23209793
MGI:5474963	M	MP:0010025	decreased total body fat amount	Mfsd2a<tm1Dls>/Mfsd2a<tm1Dls>	B6.Cg-Mfsd2a<tm1Dls>	N	23209793
MGI:5474963	M	MP:0004889	increased energy expenditure	Mfsd2a<tm1Dls>/Mfsd2a<tm1Dls>	B6.Cg-Mfsd2a<tm1Dls>	N	23209793
MGI:5474963	M	MP:0005376	homeostasis/metabolism phenotype	Mfsd2a<tm1Dls>/Mfsd2a<tm1Dls>	B6.Cg-Mfsd2a<tm1Dls>	Y	23209793
MGI:5474963	M	MP:0000598	abnormal liver morphology	Mfsd2a<tm1Dls>/Mfsd2a<tm1Dls>	B6.Cg-Mfsd2a<tm1Dls>	N	23209793
MGI:5474963	M	MP:0003961	decreased lean body mass	Mfsd2a<tm1Dls>/Mfsd2a<tm1Dls>	B6.Cg-Mfsd2a<tm1Dls>	N	23209793
MGI:5474963	M	MP:0002310	decreased susceptibility to hepatic steatosis	Mfsd2a<tm1Dls>/Mfsd2a<tm1Dls>	B6.Cg-Mfsd2a<tm1Dls>	N	23209793
MGI:5474963	M	MP:0005659	decreased susceptibility to diet-induced obesity	Mfsd2a<tm1Dls>/Mfsd2a<tm1Dls>	B6.Cg-Mfsd2a<tm1Dls>	N	23209793
MGI:5474997	M	MP:0006144	increased systemic arterial systolic blood pressure	Kcnk6<tm1Tigm>/Kcnk6<tm1Tigm>	involves: 129S5/SvEvBrd * C57BL/6	N	21876070
MGI:5474997	M	MP:0000231	hypertension	Kcnk6<tm1Tigm>/Kcnk6<tm1Tigm>	involves: 129S5/SvEvBrd * C57BL/6	N	21876070
MGI:5474997	M	MP:0004878	increased systemic vascular resistance	Kcnk6<tm1Tigm>/Kcnk6<tm1Tigm>	involves: 129S5/SvEvBrd * C57BL/6	N	21876070
MGI:5474997	M	MP:0004875	increased mean systemic arterial blood pressure	Kcnk6<tm1Tigm>/Kcnk6<tm1Tigm>	involves: 129S5/SvEvBrd * C57BL/6	N	21876070
MGI:5474997	M	MP:0006143	increased systemic arterial diastolic blood pressure	Kcnk6<tm1Tigm>/Kcnk6<tm1Tigm>	involves: 129S5/SvEvBrd * C57BL/6	N	21876070
MGI:5474997	M	MP:0005595	abnormal vascular smooth muscle physiology	Kcnk6<tm1Tigm>/Kcnk6<tm1Tigm>	involves: 129S5/SvEvBrd * C57BL/6	N	21876070
MGI:5474997	M	MP:0000250	abnormal vasoconstriction	Kcnk6<tm1Tigm>/Kcnk6<tm1Tigm>	involves: 129S5/SvEvBrd * C57BL/6	N	21876070
MGI:5475523	M	MP:0001405	impaired coordination	Cdkl5<tm1.1Joez>/Y	B6.129(FVB)-Cdkl5<tm1.1Joez>	N	23236174
MGI:5475523	M	MP:0002272	abnormal nervous system electrophysiology	Cdkl5<tm1.1Joez>/Y	B6.129(FVB)-Cdkl5<tm1.1Joez>	N	23236174
MGI:5475523	M	MP:0001513	limb grasping	Cdkl5<tm1.1Joez>/Y	B6.129(FVB)-Cdkl5<tm1.1Joez>	N	23236174
MGI:5475523	M	MP:0001399	hyperactivity	Cdkl5<tm1.1Joez>/Y	B6.129(FVB)-Cdkl5<tm1.1Joez>	N	23236174
MGI:5475523	M	MP:0009456	impaired cued conditioning behavior	Cdkl5<tm1.1Joez>/Y	B6.129(FVB)-Cdkl5<tm1.1Joez>	N	23236174
MGI:5475523	M	MP:0001361	social withdrawal	Cdkl5<tm1.1Joez>/Y	B6.129(FVB)-Cdkl5<tm1.1Joez>	N	23236174
MGI:5475523	M	MP:0001447	abnormal nest building behavior	Cdkl5<tm1.1Joez>/Y	B6.129(FVB)-Cdkl5<tm1.1Joez>	N	23236174
MGI:5475523	M	MP:0001364	decreased anxiety-related response	Cdkl5<tm1.1Joez>/Y	B6.129(FVB)-Cdkl5<tm1.1Joez>	N	23236174
MGI:5475523	M	MP:0003631	nervous system phenotype	Cdkl5<tm1.1Joez>/Y	B6.129(FVB)-Cdkl5<tm1.1Joez>	Y	23236174
MGI:5475523	M	MP:0009454	impaired contextual conditioning behavior	Cdkl5<tm1.1Joez>/Y	B6.129(FVB)-Cdkl5<tm1.1Joez>	N	23236174
MGI:5475523	M	MP:0005394	taste/olfaction phenotype	Cdkl5<tm1.1Joez>/Y	B6.129(FVB)-Cdkl5<tm1.1Joez>	Y	23236174
MGI:5475526	M	MP:0009172	small pancreatic islets	Alx3<tm1Hubr>/Alx3<tm1Hubr>	involves: 129P2/OlaHsd	N	21104068
MGI:5475526	M	MP:0013279	increased fasting circulating glucose level	Alx3<tm1Hubr>/Alx3<tm1Hubr>	involves: 129P2/OlaHsd	N	21104068
MGI:5475526	M	MP:0003059	decreased insulin secretion	Alx3<tm1Hubr>/Alx3<tm1Hubr>	involves: 129P2/OlaHsd	N	21104068
MGI:5475526	M	MP:0005293	impaired glucose tolerance	Alx3<tm1Hubr>/Alx3<tm1Hubr>	involves: 129P2/OlaHsd	N	21104068
MGI:5475526	M	MP:0003562	abnormal pancreatic beta cell physiology	Alx3<tm1Hubr>/Alx3<tm1Hubr>	involves: 129P2/OlaHsd	N	21104068
MGI:5475526	M	MP:0002079	increased circulating insulin level	Alx3<tm1Hubr>/Alx3<tm1Hubr>	involves: 129P2/OlaHsd	N	21104068
MGI:5475526	M	MP:0014117	increased pancreatic beta cell apoptosis	Alx3<tm1Hubr>/Alx3<tm1Hubr>	involves: 129P2/OlaHsd	N	21104068
MGI:5475526	M	MP:0009114	decreased pancreatic beta cell mass	Alx3<tm1Hubr>/Alx3<tm1Hubr>	involves: 129P2/OlaHsd	N	21104068
MGI:5475526	M	MP:0005376	homeostasis/metabolism phenotype	Alx3<tm1Hubr>/Alx3<tm1Hubr>	involves: 129P2/OlaHsd	Y	21104068
MGI:5475527	M	MP:0005559	increased circulating glucose level	Alx3<tm1Hubr>/Alx3<+>	involves: 129P2/OlaHsd	N	21104068
MGI:5475527	M	MP:0005293	impaired glucose tolerance	Alx3<tm1Hubr>/Alx3<+>	involves: 129P2/OlaHsd	N	21104068
MGI:5475534	M	MP:0003698	abnormal male reproductive system physiology	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6 * C57BL/6N * FVB/N * SJL	N	23267101
MGI:5475534	M	MP:0004852	decreased testis weight	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6 * C57BL/6N * FVB/N * SJL	N	23267101
MGI:5475534	M	MP:0001154	seminiferous tubule degeneration	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6 * C57BL/6N * FVB/N * SJL	N	23267101
MGI:5475535	M	MP:0005389	reproductive system phenotype	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ * SJL	Y	23267101
MGI:5475536	M	MP:0006378	abnormal spermatogonia morphology	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/N * SJL	N	23267101
MGI:5475536	M	MP:0002216	abnormal seminiferous tubule morphology	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/N * SJL	N	23267101
MGI:5475536	M	MP:0004852	decreased testis weight	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/N * SJL	N	23267101
MGI:5475536	M	MP:0001922	reduced male fertility	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/N * SJL	N	23267101
MGI:5475536	M	MP:0001156	abnormal spermatogenesis	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/N * SJL	N	23267101
MGI:5475536	M	MP:0003698	abnormal male reproductive system physiology	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/N * SJL	N	23267101
MGI:5475536	M	MP:0008261	arrest of male meiosis	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/N * SJL	N	23267101
MGI:5475536	M	MP:0001154	seminiferous tubule degeneration	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/N * SJL	N	23267101
MGI:5475536	M	MP:0001147	small testis	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/N * SJL	N	23267101
MGI:5475537	M	MP:0003698	abnormal male reproductive system physiology	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0,Tg(RARE-Hspa1b/lacZ)12Jrt/0,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * CD-1 * FVB/N * SJL	N	23267101
MGI:5475537	M	MP:0001147	small testis	Rdh10<tm1c(KOMP)Wtsi>/Rdh10<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0,Tg(RARE-Hspa1b/lacZ)12Jrt/0,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * CD-1 * FVB/N * SJL	N	23267101
MGI:5476718	M	MP:0006086	decreased body mass index	Pfas<Sofa-2J>/Pfas<+>	B6(Cg)-Pfas<Sofa-2J>/GrsrJ	N	26234751
MGI:5476718	M	MP:0003961	decreased lean body mass	Pfas<Sofa-2J>/Pfas<+>	B6(Cg)-Pfas<Sofa-2J>/GrsrJ	N	26234751
MGI:5476808	M	MP:0001925	male infertility	H3f3b<tm1.1Psk>/H3f3b<tm1.1Psk>	involves: C57BL/6N * FVB/N	N	23570311
MGI:5476808	F	MP:0001923	reduced female fertility	H3f3b<tm1.1Psk>/H3f3b<tm1.1Psk>	involves: C57BL/6N * FVB/N	N	23570311
MGI:5476839	M	MP:0000266	abnormal heart morphology	Zic3<tm1.1Smwa>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	23303524
MGI:5476839	M	MP:0000269	abnormal heart looping	Zic3<tm1.1Smwa>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	23303524
MGI:5476839	M	MP:0001695	abnormal gastrulation	Zic3<tm1.1Smwa>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	23303524
MGI:5476839	M	MP:0002151	abnormal neural tube morphology	Zic3<tm1.1Smwa>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	23303524
MGI:5476840	M	MP:0002169	no abnormal phenotype detected	Zic3<tm1.1Smwa>/Y,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>	involves: 129S7/SvEvBrd	N	23303524
MGI:5476841	M	MP:0002169	no abnormal phenotype detected	Zic3<tm1.1Smwa>/Y,Tg(Mef2c-cre)#Blk/0	Not Specified	N	23303524
MGI:5476842	M	MP:0002169	no abnormal phenotype detected	Zic3<tm1.1Smwa>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: C57BL/6J * CBA/J	N	23303524
MGI:5476843	M	MP:0002169	no abnormal phenotype detected	Zic3<tm1.1Smwa>/Y,Tg(Myh7-cre)1Jmk/0	Not Specified	N	23303524
MGI:5476844	M	MP:0000269	abnormal heart looping	Zic3<tm1.1Smwa>/Y,Tg(T-cre)1Lwd/0	involves: C3H * C57BL/6	N	23303524
MGI:5476844	M	MP:0004066	abnormal primitive node morphology	Zic3<tm1.1Smwa>/Y,Tg(T-cre)1Lwd/0	involves: C3H * C57BL/6	N	23303524
MGI:5476844	M	MP:0001706	abnormal left-right axis patterning	Zic3<tm1.1Smwa>/Y,Tg(T-cre)1Lwd/0	involves: C3H * C57BL/6	N	23303524
MGI:5476845	M	MP:0002169	no abnormal phenotype detected	Zic3<tm1.1Smwa>/Y,Tg(Nodal-cre)16Hmd/0	involves: C57BL/6	N	23303524
MGI:5477794	M	MP:0003631	nervous system phenotype	Plp1<tm1.1Blyg>/Y	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	Y	23157328
MGI:5478501	M	MP:0004802	decreased susceptibility to systemic lupus erythematosus	Fas<lpr>/Fas<lpr>,Tlr7<tm1Flv>/Y	involves: 129S1/Sv * C57BL/6 * MRL/Mp	N	16973389
MGI:5478501	M	MP:0008217	abnormal B cell activation	Fas<lpr>/Fas<lpr>,Tlr7<tm1Flv>/Y	involves: 129S1/Sv * C57BL/6 * MRL/Mp	N	16973389
MGI:5478501	M	MP:0004829	increased anti-chromatin antibody level	Fas<lpr>/Fas<lpr>,Tlr7<tm1Flv>/Y	involves: 129S1/Sv * C57BL/6 * MRL/Mp	N	16973389
MGI:5478501	M	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology	Fas<lpr>/Fas<lpr>,Tlr7<tm1Flv>/Y	involves: 129S1/Sv * C57BL/6 * MRL/Mp	N	16973389
MGI:5478501	M	MP:0008769	abnormal plasmacytoid dendritic cell physiology	Fas<lpr>/Fas<lpr>,Tlr7<tm1Flv>/Y	involves: 129S1/Sv * C57BL/6 * MRL/Mp	N	16973389
MGI:5478501	M	MP:0004953	decreased spleen weight	Fas<lpr>/Fas<lpr>,Tlr7<tm1Flv>/Y	involves: 129S1/Sv * C57BL/6 * MRL/Mp	N	16973389
MGI:5478501	M	MP:0003726	decreased autoantibody level	Fas<lpr>/Fas<lpr>,Tlr7<tm1Flv>/Y	involves: 129S1/Sv * C57BL/6 * MRL/Mp	N	16973389
MGI:5478501	M	MP:0000701	abnormal lymph node size	Fas<lpr>/Fas<lpr>,Tlr7<tm1Flv>/Y	involves: 129S1/Sv * C57BL/6 * MRL/Mp	N	16973389
MGI:5478501	M	MP:0008498	decreased IgG3 level	Fas<lpr>/Fas<lpr>,Tlr7<tm1Flv>/Y	involves: 129S1/Sv * C57BL/6 * MRL/Mp	N	16973389
MGI:5478501	M	MP:0005089	decreased double-negative T cell number	Fas<lpr>/Fas<lpr>,Tlr7<tm1Flv>/Y	involves: 129S1/Sv * C57BL/6 * MRL/Mp	N	16973389
MGI:5478501	M	MP:0008496	decreased IgG2a level	Fas<lpr>/Fas<lpr>,Tlr7<tm1Flv>/Y	involves: 129S1/Sv * C57BL/6 * MRL/Mp	N	16973389
MGI:5478501	M	MP:0003725	increased autoantibody level	Fas<lpr>/Fas<lpr>,Tlr7<tm1Flv>/Y	involves: 129S1/Sv * C57BL/6 * MRL/Mp	N	16973389
MGI:5478546	M	MP:0002169	no abnormal phenotype detected	Cxcr3<tm1Arsa>/Y	involves: 129S4/SvJae	N	23338236
MGI:5478551	M	MP:0001935	decreased litter size	Bub1<tm3.1Jvd>/Bub1<tm3.1Jvd>	involves: 129S4/SvJae * C57BL/6	N	23209306
MGI:5478551	M	MP:0001922	reduced male fertility	Bub1<tm3.1Jvd>/Bub1<tm3.1Jvd>	involves: 129S4/SvJae * C57BL/6	N	23209306
MGI:5478551	M	MP:0001153	small seminiferous tubules	Bub1<tm3.1Jvd>/Bub1<tm3.1Jvd>	involves: 129S4/SvJae * C57BL/6	N	23209306
MGI:5478551	M	MP:0002687	oligozoospermia	Bub1<tm3.1Jvd>/Bub1<tm3.1Jvd>	involves: 129S4/SvJae * C57BL/6	N	23209306
MGI:5478551	M	MP:0001147	small testis	Bub1<tm3.1Jvd>/Bub1<tm3.1Jvd>	involves: 129S4/SvJae * C57BL/6	N	23209306
MGI:5478551	M	MP:0004852	decreased testis weight	Bub1<tm3.1Jvd>/Bub1<tm3.1Jvd>	involves: 129S4/SvJae * C57BL/6	N	23209306
MGI:5478560	M	MP:0003329	amyloid beta deposits	Tg(Camk2a-tTA)1Mmay/0,Tg(tetO-APPSwInd)107Dbo/0	(FVB/NJ x B6.Cg-Tg(tetO-APPSwInd)107Dbo Tg(Camk2a-tTA)1Mmay)F1	N	23447589
MGI:5478560	M	MP:0008432	abnormal long-term spatial reference memory	Tg(Camk2a-tTA)1Mmay/0,Tg(tetO-APPSwInd)107Dbo/0	(FVB/NJ x B6.Cg-Tg(tetO-APPSwInd)107Dbo Tg(Camk2a-tTA)1Mmay)F1	N	23447589
MGI:5478560	M	MP:0014370	impaired spatial working memory	Tg(Camk2a-tTA)1Mmay/0,Tg(tetO-APPSwInd)107Dbo/0	(FVB/NJ x B6.Cg-Tg(tetO-APPSwInd)107Dbo Tg(Camk2a-tTA)1Mmay)F1	N	23447589
MGI:5478560	M	MP:0005386	behavior/neurological phenotype	Tg(Camk2a-tTA)1Mmay/0,Tg(tetO-APPSwInd)107Dbo/0	(FVB/NJ x B6.Cg-Tg(tetO-APPSwInd)107Dbo Tg(Camk2a-tTA)1Mmay)F1	Y	23447589
MGI:5478589	F	MP:0004993	decreased bone resorption	Siglec15<tm1Yohi>/Siglec15<tm1Yohi>	B6.129S6-Siglec15<tm1Yohi>	N	23238125
MGI:5478589	F	MP:0010967	increased compact bone area	Siglec15<tm1Yohi>/Siglec15<tm1Yohi>	B6.129S6-Siglec15<tm1Yohi>	N	23238125
MGI:5478589	F	MP:0030984	increased circulating osteocalcin level	Siglec15<tm1Yohi>/Siglec15<tm1Yohi>	B6.129S6-Siglec15<tm1Yohi>	N	23238125
MGI:5478754	F	MP:0010579	increased heart left ventricle size	Adam17<tm1.1Rain>/Adam17<tm1.2Rain>,Tg(Tek-cre)12Flv/0	B6.Cg-Adam17<tm1.1Rain> Adam17<tm1.2Rain> Tg(Tek-cre)12Flv	N	23354118
MGI:5478754	F	MP:0002626	increased heart rate	Adam17<tm1.1Rain>/Adam17<tm1.2Rain>,Tg(Tek-cre)12Flv/0	B6.Cg-Adam17<tm1.1Rain> Adam17<tm1.2Rain> Tg(Tek-cre)12Flv	N	23354118
MGI:5478754	F	MP:0011929	abnormal aortic valve flow	Adam17<tm1.1Rain>/Adam17<tm1.2Rain>,Tg(Tek-cre)12Flv/0	B6.Cg-Adam17<tm1.1Rain> Adam17<tm1.2Rain> Tg(Tek-cre)12Flv	N	23354118
MGI:5484566	M	MP:0004811	abnormal neuron physiology	Hltf<tm1.1Arte>/Hltf<tm1.1Arte>	Not Specified	N	23415230
MGI:5484566	M	MP:0009747	impaired behavioral response to xenobiotic	Hltf<tm1.1Arte>/Hltf<tm1.1Arte>	Not Specified	N	23415230
MGI:5484566	M	MP:0004948	abnormal neuronal precursor proliferation	Hltf<tm1.1Arte>/Hltf<tm1.1Arte>	Not Specified	N	23415230
MGI:5486002	F	MP:0031115	macrovesicular hepatic steatosis	Macroh2a1<tm1Mbou>/Macroh2a1<tm1Mbou>	involves: 129P2/OlaHsd * C57BL/6	N	20359320
MGI:5486142	M	MP:0009142	decreased prepulse inhibition	Tg(Camk2a-DISC1)37Asaw/0	C57BL/6-Tg(Camk2a-DISC1)37Asaw	N	17675407
MGI:5486142	M	MP:0001399	hyperactivity	Tg(Camk2a-DISC1)37Asaw/0	C57BL/6-Tg(Camk2a-DISC1)37Asaw	N	17675407
MGI:5486142	M	MP:0001522	impaired swimming	Tg(Camk2a-DISC1)37Asaw/0	C57BL/6-Tg(Camk2a-DISC1)37Asaw	N	17675407
MGI:5486142	M	MP:0004924	abnormal behavior	Tg(Camk2a-DISC1)37Asaw/0	C57BL/6-Tg(Camk2a-DISC1)37Asaw	N	17675407
MGI:5486142	M	MP:0000822	abnormal brain ventricle morphology	Tg(Camk2a-DISC1)37Asaw/0	C57BL/6-Tg(Camk2a-DISC1)37Asaw	N	17675407
MGI:5486199	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(ARR2/Pbsn-MYC)7Key/?	involves: FVB/N	N	14522256
MGI:5486199	M	MP:0010357	increased prostate gland tumor incidence	Tg(ARR2/Pbsn-MYC)7Key/?	involves: FVB/N	N	14522256
MGI:5486199	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(ARR2/Pbsn-MYC)7Key/?	involves: FVB/N	N	26029871
MGI:5486199	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(ARR2/Pbsn-MYC)7Key/?	involves: FVB/N	N	14522256
MGI:5486199	M	MP:0004958	enlarged prostate gland	Tg(ARR2/Pbsn-MYC)7Key/?	involves: FVB/N	N	26029871
MGI:5486199	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(ARR2/Pbsn-MYC)7Key/?	involves: FVB/N	N	26029871
MGI:5486218	F	MP:0003718	maternal effect	Ube2q1<tm1Grz>/Ube2q1<tm1Grz>	involves: 129S1/Sv * 129X1/SvJ	N	23108111
MGI:5486218	F	MP:0001382	abnormal nursing	Ube2q1<tm1Grz>/Ube2q1<tm1Grz>	involves: 129S1/Sv * 129X1/SvJ	N	23108111
MGI:5486218	F	MP:0008976	delayed female fertility	Ube2q1<tm1Grz>/Ube2q1<tm1Grz>	involves: 129S1/Sv * 129X1/SvJ	N	23108111
MGI:5486218	F	MP:0001377	abnormal mating frequency	Ube2q1<tm1Grz>/Ube2q1<tm1Grz>	involves: 129S1/Sv * 129X1/SvJ	N	23108111
MGI:5486218	F	MP:0009011	prolonged diestrus	Ube2q1<tm1Grz>/Ube2q1<tm1Grz>	involves: 129S1/Sv * 129X1/SvJ	N	23108111
MGI:5486218	F	MP:0005121	decreased circulating prolactin level	Ube2q1<tm1Grz>/Ube2q1<tm1Grz>	involves: 129S1/Sv * 129X1/SvJ	N	23108111
MGI:5486337	F	MP:0002816	colitis	Nox1<tm1.1Anrt>/Nox1<tm1.1Anrt>,Tg(Vil1-cre)997Gum/0	involves: C57BL/6J * SJL	N	23241962
MGI:5486337	F	MP:0005023	abnormal wound healing	Nox1<tm1.1Anrt>/Nox1<tm1.1Anrt>,Tg(Vil1-cre)997Gum/0	involves: C57BL/6J * SJL	N	23241962
MGI:5486337	F	MP:0003186	abnormal redox activity	Nox1<tm1.1Anrt>/Nox1<tm1.1Anrt>,Tg(Vil1-cre)997Gum/0	involves: C57BL/6J * SJL	N	23241962
MGI:5486338	F	MP:0005376	homeostasis/metabolism phenotype	Cybb<tm1Din>/Cybb<tm1Din>	B6.129S-Cybb<tm1Din>/J	Y	23241962
MGI:5487278	F	MP:0009763	increased susceptibility to induced morbidity/mortality	Cacna1a<tm3Maag>/Cacna1a<+>	involves: 129P2/OlaHsd	N	22144569
MGI:5487449	M	MP:0005244	hemopericardium	Tmsb4x<tm1Prri>/Tmsb4x<tm1Prri>	B6.129-Tmsb4x<tm1Prri>	N	22723298
MGI:5487449	M	MP:0011401	abnormal vascular smooth muscle development	Tmsb4x<tm1Prri>/Tmsb4x<tm1Prri>	B6.129-Tmsb4x<tm1Prri>	N	22723298
MGI:5487449	M	MP:0009698	heart hemorrhage	Tmsb4x<tm1Prri>/Tmsb4x<tm1Prri>	B6.129-Tmsb4x<tm1Prri>	N	22723298
MGI:5487449	M	MP:0005391	vision/eye phenotype	Tmsb4x<tm1Prri>/Tmsb4x<tm1Prri>	B6.129-Tmsb4x<tm1Prri>	Y	22723298
MGI:5487449	M	MP:0001614	abnormal blood vessel morphology	Tmsb4x<tm1Prri>/Tmsb4x<tm1Prri>	B6.129-Tmsb4x<tm1Prri>	N	22723298
MGI:5487449	M	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Tmsb4x<tm1Prri>/Tmsb4x<tm1Prri>	B6.129-Tmsb4x<tm1Prri>	N	22723298
MGI:5487449	M	MP:0002652	thin myocardium	Tmsb4x<tm1Prri>/Tmsb4x<tm1Prri>	B6.129-Tmsb4x<tm1Prri>	N	22723298
MGI:5487449	M	MP:0001915	intracranial hemorrhage	Tmsb4x<tm1Prri>/Tmsb4x<tm1Prri>	B6.129-Tmsb4x<tm1Prri>	N	22723298
MGI:5487449	M	MP:0004112	abnormal arteriole morphology	Tmsb4x<tm1Prri>/Tmsb4x<tm1Prri>	B6.129-Tmsb4x<tm1Prri>	N	22723298
MGI:5487449	M	MP:0001634	internal hemorrhage	Tmsb4x<tm1Prri>/Tmsb4x<tm1Prri>	B6.129-Tmsb4x<tm1Prri>	N	22723298
MGI:5487450	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Tmsb4x<tm1Prri>/Y	B6.129-Tmsb4x<tm1Prri>	N	22723298
MGI:5487451	F	MP:0001634	internal hemorrhage	Hprt1<tm1(H1-RNAi:Tmsb4x)Prri>/Hprt1<+>,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	22723298
MGI:5487451	F	MP:0001614	abnormal blood vessel morphology	Hprt1<tm1(H1-RNAi:Tmsb4x)Prri>/Hprt1<+>,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	22723298
MGI:5487451	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Hprt1<tm1(H1-RNAi:Tmsb4x)Prri>/Hprt1<+>,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	22723298
MGI:5487451	F	MP:0005244	hemopericardium	Hprt1<tm1(H1-RNAi:Tmsb4x)Prri>/Hprt1<+>,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	22723298
MGI:5487451	F	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance	Hprt1<tm1(H1-RNAi:Tmsb4x)Prri>/Hprt1<+>,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	22723298
MGI:5487451	F	MP:0001915	intracranial hemorrhage	Hprt1<tm1(H1-RNAi:Tmsb4x)Prri>/Hprt1<+>,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	22723298
MGI:5487581	F	MP:0010868	increased bone trabecula number	Slc5a1<Gt(OST315271)Lex>/Slc5a1<Gt(OST315271)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	23149623
MGI:5487581	F	MP:0004348	long femur	Slc5a1<Gt(OST315271)Lex>/Slc5a1<Gt(OST315271)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	23149623
MGI:5487582	F	MP:0000062	increased bone mineral density	Slc5a2<tm1Lex>/Slc5a2<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	23149623
MGI:5487582	F	MP:0010868	increased bone trabecula number	Slc5a2<tm1Lex>/Slc5a2<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	23149623
MGI:5487583	M	MP:0005619	increased urine potassium level	Slc5a1<Gt(OST315271)Lex>/Slc5a1<Gt(OST315271)Lex>,Slc5a2<tm1Lex>/Slc5a2<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	23149623
MGI:5487583	M	MP:0011939	increased food intake	Slc5a1<Gt(OST315271)Lex>/Slc5a1<Gt(OST315271)Lex>,Slc5a2<tm1Lex>/Slc5a2<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	23149623
MGI:5487583	M	MP:0001262	decreased body weight	Slc5a1<Gt(OST315271)Lex>/Slc5a1<Gt(OST315271)Lex>,Slc5a2<tm1Lex>/Slc5a2<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	23149623
MGI:5487583	M	MP:0010025	decreased total body fat amount	Slc5a1<Gt(OST315271)Lex>/Slc5a1<Gt(OST315271)Lex>,Slc5a2<tm1Lex>/Slc5a2<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	23149623
MGI:5487583	M	MP:0011459	increased urine chloride ion level	Slc5a1<Gt(OST315271)Lex>/Slc5a1<Gt(OST315271)Lex>,Slc5a2<tm1Lex>/Slc5a2<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	23149623
MGI:5487583	M	MP:0011466	increased urine urea nitrogen level	Slc5a1<Gt(OST315271)Lex>/Slc5a1<Gt(OST315271)Lex>,Slc5a2<tm1Lex>/Slc5a2<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	23149623
MGI:5487807	F	MP:0003871	abnormal myelin sheath morphology	Gpm6b<tm1Kan>/Gpm6b<tm1Kan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487807	F	MP:0005404	abnormal axon morphology	Gpm6b<tm1Kan>/Gpm6b<tm1Kan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487807	F	MP:0005386	behavior/neurological phenotype	Gpm6b<tm1Kan>/Gpm6b<tm1Kan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	23322581
MGI:5487808	M	MP:0005386	behavior/neurological phenotype	Gpm6b<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	23322581
MGI:5487808	M	MP:0005404	abnormal axon morphology	Gpm6b<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487808	M	MP:0003871	abnormal myelin sheath morphology	Gpm6b<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0001393	ataxia	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0001505	hunched posture	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0003224	neuron degeneration	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0000920	abnormal myelination	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0000953	abnormal oligodendrocyte morphology	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0005405	axon degeneration	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0008226	decreased anterior commissure size	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0005377	hearing/vestibular/ear phenotype	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	23322581
MGI:5487810	M	MP:0000921	demyelination	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0010749	absent visual evoked potential	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0003354	astrocytosis	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0004143	muscle hypertonia	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0003983	decreased cholesterol level	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0006325	impaired hearing	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0011966	abnormal auditory brainstem response waveform shape	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0008918	microgliosis	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0003634	abnormal glial cell morphology	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0003871	abnormal myelin sheath morphology	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0006042	increased apoptosis	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0011380	enlarged brain ventricles	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0001388	abnormal stationary movement	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0008026	abnormal brain white matter morphology	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0000745	tremors	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0002083	premature death	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0001516	abnormal motor coordination/balance	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0000781	decreased corpus callosum size	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0010205	abnormal oligodendrocyte apoptosis	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0001326	retina degeneration	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487810	M	MP:0000743	muscle spasm	Gpm6b<tm1Kan> Plp1<tm1Kan>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487811	F	MP:0002066	abnormal motor capabilities/coordination/movement	Gpm6b<tm1Kan>/Gpm6b<tm1Kan>,Plp1<tm1Kan>/Plp1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487811	F	MP:0002083	premature death	Gpm6b<tm1Kan>/Gpm6b<tm1Kan>,Plp1<tm1Kan>/Plp1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487812	F	MP:0002066	abnormal motor capabilities/coordination/movement	Gpm6b<tm1Kan>/Gpm6b<+>,Plp1<tm1Kan>/Plp1<tm1Kan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5487812	F	MP:0002083	premature death	Gpm6b<tm1Kan>/Gpm6b<+>,Plp1<tm1Kan>/Plp1<tm1Kan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23322581
MGI:5488500	M	MP:0005397	hematopoietic system phenotype	Tlr7<tm1Flv>/Y,X/Yaa	B6.Cg-Tlr7<tm1Flv> Yaa	Y	17997333
MGI:5488504	M	MP:0008182	decreased marginal zone B cell number	X/Yaa	B6.SB-Yaa/J	N	17997333
MGI:5488504	M	MP:0009336	increased splenocyte proliferation	X/Yaa	B6.SB-Yaa/J	N	17997333
MGI:5488507	M	MP:0009335	decreased splenocyte proliferation	Tlr7<tm1Flv>/Y	B6.129S1-Tlr7<tm1Flv>	N	17997333
MGI:5488507	M	MP:0008181	increased marginal zone B cell number	Tlr7<tm1Flv>/Y	B6.129S1-Tlr7<tm1Flv>	N	17997333
MGI:5488508	M	MP:0009333	abnormal splenocyte physiology	Fcgr2b<tm1Ttk>/Fcgr2b<tm1Ttk>,Tlr7<tm1Flv>/Y,X/Yaa	B6.Cg-Fcgr2b<tm1Ttk> Tlr7<tm1Flv> Yaa	N	17997333
MGI:5488508	M	MP:0002083	premature death	Fcgr2b<tm1Ttk>/Fcgr2b<tm1Ttk>,Tlr7<tm1Flv>/Y,X/Yaa	B6.Cg-Fcgr2b<tm1Ttk> Tlr7<tm1Flv> Yaa	N	17997333
MGI:5488508	M	MP:0002135	abnormal kidney morphology	Fcgr2b<tm1Ttk>/Fcgr2b<tm1Ttk>,Tlr7<tm1Flv>/Y,X/Yaa	B6.Cg-Fcgr2b<tm1Ttk> Tlr7<tm1Flv> Yaa	N	17997333
MGI:5488508	M	MP:0000691	enlarged spleen	Fcgr2b<tm1Ttk>/Fcgr2b<tm1Ttk>,Tlr7<tm1Flv>/Y,X/Yaa	B6.Cg-Fcgr2b<tm1Ttk> Tlr7<tm1Flv> Yaa	N	17997333
MGI:5488508	M	MP:0004801	increased susceptibility to systemic lupus erythematosus	Fcgr2b<tm1Ttk>/Fcgr2b<tm1Ttk>,Tlr7<tm1Flv>/Y,X/Yaa	B6.Cg-Fcgr2b<tm1Ttk> Tlr7<tm1Flv> Yaa	N	17997333
MGI:5488508	M	MP:0004794	increased anti-nuclear antigen antibody level	Fcgr2b<tm1Ttk>/Fcgr2b<tm1Ttk>,Tlr7<tm1Flv>/Y,X/Yaa	B6.Cg-Fcgr2b<tm1Ttk> Tlr7<tm1Flv> Yaa	N	17997333
MGI:5488508	M	MP:0001844	autoimmune response	Fcgr2b<tm1Ttk>/Fcgr2b<tm1Ttk>,Tlr7<tm1Flv>/Y,X/Yaa	B6.Cg-Fcgr2b<tm1Ttk> Tlr7<tm1Flv> Yaa	N	17997333
MGI:5488509	M	MP:0000691	enlarged spleen	Fcgr2b<tm1Ttk>/Fcgr2b<tm1Ttk>,X/Yaa	B6.Cg-Fcgr2b<tm1Ttk> Yaa	N	17997333
MGI:5488509	M	MP:0001844	autoimmune response	Fcgr2b<tm1Ttk>/Fcgr2b<tm1Ttk>,X/Yaa	B6.Cg-Fcgr2b<tm1Ttk> Yaa	N	17997333
MGI:5488509	M	MP:0002135	abnormal kidney morphology	Fcgr2b<tm1Ttk>/Fcgr2b<tm1Ttk>,X/Yaa	B6.Cg-Fcgr2b<tm1Ttk> Yaa	N	17997333
MGI:5488509	M	MP:0004801	increased susceptibility to systemic lupus erythematosus	Fcgr2b<tm1Ttk>/Fcgr2b<tm1Ttk>,X/Yaa	B6.Cg-Fcgr2b<tm1Ttk> Yaa	N	17997333
MGI:5488509	M	MP:0004794	increased anti-nuclear antigen antibody level	Fcgr2b<tm1Ttk>/Fcgr2b<tm1Ttk>,X/Yaa	B6.Cg-Fcgr2b<tm1Ttk> Yaa	N	17997333
MGI:5488509	M	MP:0002083	premature death	Fcgr2b<tm1Ttk>/Fcgr2b<tm1Ttk>,X/Yaa	B6.Cg-Fcgr2b<tm1Ttk> Yaa	N	17997333
MGI:5488511	M	MP:0005461	abnormal dendritic cell morphology	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488511	M	MP:0008182	decreased marginal zone B cell number	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488511	M	MP:0002083	premature death	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488511	M	MP:0008210	increased mature B cell number	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488511	M	MP:0000691	enlarged spleen	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488511	M	MP:0009336	increased splenocyte proliferation	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488511	M	MP:0001844	autoimmune response	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488511	M	MP:0001860	liver inflammation	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488511	M	MP:0001828	abnormal T cell activation	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488511	M	MP:0002743	glomerulonephritis	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488511	M	MP:0004794	increased anti-nuclear antigen antibody level	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488511	M	MP:0004939	abnormal B cell morphology	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488511	M	MP:0001861	lung inflammation	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488511	M	MP:0008217	abnormal B cell activation	X/Tg(Tlr7)6Boll	involves: C57BL/6	N	17997333
MGI:5488618	f	MP:0004748	increased susceptibility to age-related hearing loss	Tg(CAG-Tfb1m)AGsha/?	involves: C57BL/6J * SJL/J	N	22341444
MGI:5488618	f	MP:0006325	impaired hearing	Tg(CAG-Tfb1m)AGsha/?	involves: C57BL/6J * SJL/J	N	22341444
MGI:5488618	f	MP:0011967	increased or absent threshold for auditory brainstem response	Tg(CAG-Tfb1m)AGsha/?	involves: C57BL/6J * SJL/J	N	22341444
MGI:5488618	f	MP:0003703	abnormal vestibulocochlear ganglion morphology	Tg(CAG-Tfb1m)AGsha/?	involves: C57BL/6J * SJL/J	N	22341444
MGI:5488619	f	MP:0005377	hearing/vestibular/ear phenotype	E2f1<tm1Meg>/E2f1<+>,Tg(CAG-Tfb1m)AGsha/0	involves: 129S4/SvJae * C57BL/6J * SJL/J	Y	22341444
MGI:5488641	M	MP:0002169	no abnormal phenotype detected	Kdm6a<tm1.1Kaig>/Y	involves: 129S4/SvJaeSor	N	22949634
MGI:5489776	F	MP:0001923	reduced female fertility	Alx3<tm1Hubr>/Alx3<tm1Hubr>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	20534379
MGI:5490539	M	MP:0005169	abnormal male meiosis	Spo11<tm2.1Rdco>/Spo11<tm2.1Rdco>	B6.129S6-Spo11<tm2.1Rdco>	N	23318132
MGI:5490539	M	MP:0008261	arrest of male meiosis	Spo11<tm2.1Rdco>/Spo11<tm2.1Rdco>	B6.129S6-Spo11<tm2.1Rdco>	N	23318132
MGI:5490540	M	MP:0005169	abnormal male meiosis	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6	N	23318132
MGI:5490541	M	MP:0005169	abnormal male meiosis	Mei1<m1Jcs>/Mei1<m1Jcs>	involves: 129S1/Sv	N	23318132
MGI:5490542	M	MP:0005169	abnormal male meiosis	Sun1<tm1.1Ktj>/Sun1<tm1.1Ktj>	Not Specified	N	23318132
MGI:5490769	F	MP:0005376	homeostasis/metabolism phenotype	Heph<tm1.1Jdun>/Heph<tm1.1Jdun>,Tg(BEST1-cre)1Jdun/0	involves: C57BL/6 * C57BL/6NTac	Y	22342521
MGI:5490770	F	MP:0000367	abnormal coat/ hair morphology	Heph<tm1.2Jdun>/Heph<tm1.2Jdun>	involves: C57BL/6 * C57BL/6NTac	N	22342521
MGI:5490771	F	MP:0001770	abnormal iron level	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<tm1.2Jdun>/Heph<tm1.2Jdun>	involves: 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	22342521
MGI:5490771	F	MP:0002229	neurodegeneration	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<tm1.2Jdun>/Heph<tm1.2Jdun>	involves: 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	22342521
MGI:5490771	F	MP:0001577	anemia	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<tm1.2Jdun>/Heph<tm1.2Jdun>	involves: 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	22342521
MGI:5490772	F	MP:0005201	abnormal retina pigment epithelium morphology	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<tm1.1Jdun>/Heph<tm1.1Jdun>,Tg(BEST1-cre)1Jdun/0	involves: 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	22342521
MGI:5490772	F	MP:0005548	retina pigment epithelium atrophy	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<tm1.1Jdun>/Heph<tm1.1Jdun>,Tg(BEST1-cre)1Jdun/0	involves: 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	22342521
MGI:5490772	F	MP:0001770	abnormal iron level	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<tm1.1Jdun>/Heph<tm1.1Jdun>,Tg(BEST1-cre)1Jdun/0	involves: 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	22342521
MGI:5490773	F	MP:0005376	homeostasis/metabolism phenotype	Heph<tm1.1Jdun>/Heph<tm1.1Jdun>,Tg(Rho-cre)#Yzl/0	involves: C57BL/6NTac	Y	22342521
MGI:5490774	F	MP:0005376	homeostasis/metabolism phenotype	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<tm1.1Jdun>/Heph<tm1.1Jdun>,Tg(Rho-cre)#Yzl/0	involves: 129X1/SvJ * C57BL/6NTac	Y	22342521
MGI:5490775	F	MP:0001770	abnormal iron level	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<tm1.1Jdun>/Heph<tm1.1Jdun>,Tg(BEST1-cre)1Jdun/0,Tg(Rho-cre)#Yzl/0	involves: 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	22342521
MGI:5490775	F	MP:0008469	abnormal protein level	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<tm1.1Jdun>/Heph<tm1.1Jdun>,Tg(BEST1-cre)1Jdun/0,Tg(Rho-cre)#Yzl/0	involves: 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	22342521
MGI:5490776	F	MP:0001770	abnormal iron level	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Heph<sla>	involves: 129X1/SvJ	N	22342521
MGI:5490776	F	MP:0004151	decreased circulating iron level	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Heph<sla>	involves: 129X1/SvJ	N	22342521
MGI:5490776	F	MP:0005201	abnormal retina pigment epithelium morphology	Cp<tm1Hrs>/Cp<tm1Hrs>,Heph<sla>/Heph<sla>	involves: 129X1/SvJ	N	22342521
MGI:5491040	M	MP:0000807	abnormal hippocampus morphology	Mecp2<tm1.1Bird>/Y,Tg(MECP2*R270X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491040	M	MP:0002083	premature death	Mecp2<tm1.1Bird>/Y,Tg(MECP2*R270X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491040	M	MP:0000788	abnormal cerebral cortex morphology	Mecp2<tm1.1Bird>/Y,Tg(MECP2*R270X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491040	M	MP:0001260	increased body weight	Mecp2<tm1.1Bird>/Y,Tg(MECP2*R270X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491040	M	MP:0001406	abnormal gait	Mecp2<tm1.1Bird>/Y,Tg(MECP2*R270X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491040	M	MP:0002175	decreased brain weight	Mecp2<tm1.1Bird>/Y,Tg(MECP2*R270X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491040	M	MP:0001511	disheveled coat	Mecp2<tm1.1Bird>/Y,Tg(MECP2*R270X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491040	M	MP:0000913	abnormal brain development	Mecp2<tm1.1Bird>/Y,Tg(MECP2*R270X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491040	M	MP:0000745	tremors	Mecp2<tm1.1Bird>/Y,Tg(MECP2*R270X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491041	M	MP:0000788	abnormal cerebral cortex morphology	Mecp2<tm1.1Bird>/Y,Tg(MECP2*G273X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491041	M	MP:0001406	abnormal gait	Mecp2<tm1.1Bird>/Y,Tg(MECP2*G273X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491041	M	MP:0002083	premature death	Mecp2<tm1.1Bird>/Y,Tg(MECP2*G273X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491041	M	MP:0001260	increased body weight	Mecp2<tm1.1Bird>/Y,Tg(MECP2*G273X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491041	M	MP:0000807	abnormal hippocampus morphology	Mecp2<tm1.1Bird>/Y,Tg(MECP2*G273X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491041	M	MP:0002175	decreased brain weight	Mecp2<tm1.1Bird>/Y,Tg(MECP2*G273X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491041	M	MP:0000913	abnormal brain development	Mecp2<tm1.1Bird>/Y,Tg(MECP2*G273X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491041	M	MP:0000745	tremors	Mecp2<tm1.1Bird>/Y,Tg(MECP2*G273X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491042	M	MP:0002169	no abnormal phenotype detected	Tg(MECP2*R270X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491043	M	MP:0002169	no abnormal phenotype detected	Tg(MECP2*G273X/GFP)AHzo/0	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491051	M	MP:0000913	abnormal brain development	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491051	M	MP:0000788	abnormal cerebral cortex morphology	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491051	M	MP:0002083	premature death	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491051	M	MP:0000807	abnormal hippocampus morphology	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491051	M	MP:0001406	abnormal gait	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491051	M	MP:0000745	tremors	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491051	M	MP:0002175	decreased brain weight	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491051	M	MP:0001260	increased body weight	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491051	M	MP:0001511	disheveled coat	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * FVB	N	23452848
MGI:5491870	M	MP:0010768	mortality/aging	L1cam<tm2.1Vlem>/Y	either: 129S4.129S2-L1cam<tm2.1Vlem> or B6.129S4-L1cam<tm2.1Vlem>	Y	20127821
MGI:5491870	M	MP:0005386	behavior/neurological phenotype	L1cam<tm2.1Vlem>/Y	either: 129S4.129S2-L1cam<tm2.1Vlem> or B6.129S4-L1cam<tm2.1Vlem>	Y	20127821
MGI:5491870	M	MP:0003631	nervous system phenotype	L1cam<tm2.1Vlem>/Y	either: 129S4.129S2-L1cam<tm2.1Vlem> or B6.129S4-L1cam<tm2.1Vlem>	Y	20127821
MGI:5491871	M	MP:0010768	mortality/aging	L1cam<tm3.1Vlem>/Y	either: 129S4.129S2-L1cam<tm3.1Vlem> or B6.129S4-L1cam<tm3.1Vlem>	Y	20127821
MGI:5491871	M	MP:0008415	abnormal neurite morphology	L1cam<tm3.1Vlem>/Y	either: 129S4.129S2-L1cam<tm3.1Vlem> or B6.129S4-L1cam<tm3.1Vlem>	N	20127821
MGI:5491871	M	MP:0005386	behavior/neurological phenotype	L1cam<tm3.1Vlem>/Y	either: 129S4.129S2-L1cam<tm3.1Vlem> or B6.129S4-L1cam<tm3.1Vlem>	Y	20127821
MGI:5491871	M	MP:0003631	nervous system phenotype	L1cam<tm3.1Vlem>/Y	either: 129S4.129S2-L1cam<tm3.1Vlem> or B6.129S4-L1cam<tm3.1Vlem>	Y	20127821
MGI:5491871	M	MP:0001405	impaired coordination	L1cam<tm3.1Vlem>/Y	either: 129S4.129S2-L1cam<tm3.1Vlem> or B6.129S4-L1cam<tm3.1Vlem>	N	20127821
MGI:5491872	M	MP:0003631	nervous system phenotype	L1cam<tm4.1Vlem>/Y	either: 129S4.129S2-L1cam<tm4.1Vlem> or B6.129S4-L1cam<tm4.1Vlem>	Y	20127821
MGI:5491872	M	MP:0010768	mortality/aging	L1cam<tm4.1Vlem>/Y	either: 129S4.129S2-L1cam<tm4.1Vlem> or B6.129S4-L1cam<tm4.1Vlem>	Y	20127821
MGI:5491872	M	MP:0005386	behavior/neurological phenotype	L1cam<tm4.1Vlem>/Y	either: 129S4.129S2-L1cam<tm4.1Vlem> or B6.129S4-L1cam<tm4.1Vlem>	Y	20127821
MGI:5491872	M	MP:0008415	abnormal neurite morphology	L1cam<tm4.1Vlem>/Y	either: 129S4.129S2-L1cam<tm4.1Vlem> or B6.129S4-L1cam<tm4.1Vlem>	N	20127821
MGI:5491872	M	MP:0001405	impaired coordination	L1cam<tm4.1Vlem>/Y	either: 129S4.129S2-L1cam<tm4.1Vlem> or B6.129S4-L1cam<tm4.1Vlem>	N	20127821
MGI:5492338	F	MP:0001265	decreased body size	Phex<m1Jrt>/Phex<+>	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492338	F	MP:0001262	decreased body weight	Phex<m1Jrt>/Phex<+>	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492338	F	MP:0002968	increased circulating alkaline phosphatase level	Phex<m1Jrt>/Phex<+>	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492338	F	MP:0000195	decreased circulating calcium level	Phex<m1Jrt>/Phex<+>	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492338	F	MP:0011505	camptomelia	Phex<m1Jrt>/Phex<+>	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492338	F	MP:0004686	decreased length of long bones	Phex<m1Jrt>/Phex<+>	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492338	F	MP:0002932	abnormal joint morphology	Phex<m1Jrt>/Phex<+>	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492338	F	MP:0001258	decreased body length	Phex<m1Jrt>/Phex<+>	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492338	F	MP:0000198	decreased circulating phosphate level	Phex<m1Jrt>/Phex<+>	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492338	F	MP:0004610	small vertebrae	Phex<m1Jrt>/Phex<+>	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492338	F	MP:0004509	abnormal pelvic girdle bone morphology	Phex<m1Jrt>/Phex<+>	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492341	M	MP:0003797	abnormal compact bone morphology	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492341	M	MP:0001262	decreased body weight	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492341	M	MP:0005390	skeleton phenotype	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	Y	22573557
MGI:5492341	M	MP:0009445	osteomalacia	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492341	M	MP:0010924	abnormal osteoid morphology	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492341	M	MP:0008152	decreased diameter of femur	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492341	M	MP:0000063	decreased bone mineral density	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492341	M	MP:0003662	abnormal long bone epiphyseal plate proliferative zone	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492341	M	MP:0002968	increased circulating alkaline phosphatase level	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492341	M	MP:0006398	increased long bone epiphyseal plate size	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492341	M	MP:0010124	decreased bone mineral content	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492341	M	MP:0003055	abnormal long bone epiphyseal plate morphology	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492341	M	MP:0000195	decreased circulating calcium level	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5492341	M	MP:0000198	decreased circulating phosphate level	Phex<m1Jrt>/Y	B6.129S1-Phex<M1Jrt>	N	22573557
MGI:5494250	F	MP:0003651	abnormal axon extension	Vamp7<tm1.1Aha>/Vamp7<tm1.1Aha>	involves: 129S4/SvJae	N	21740490
MGI:5494251	M	MP:0003651	abnormal axon extension	Vamp7<tm1.1Aha>/Y	involves: 129S4/SvJae	N	21740490
MGI:5494451	M	MP:0001925	male infertility	Brca1<tm2Rjbr>/Brca1<tm2Rjbr>	involves: 129 * C57BL/6	N	22034435
MGI:5494453	M	MP:0001925	male infertility	Brca1<tm3.1Rjbr>/Brca1<tm3.1Rjbr>	involves: 129 * C57BL/6	N	22034435
MGI:5494453	M	MP:0005159	azoospermia	Brca1<tm3.1Rjbr>/Brca1<tm3.1Rjbr>	involves: 129 * C57BL/6	N	22034435
MGI:5494453	M	MP:0001155	arrest of spermatogenesis	Brca1<tm3.1Rjbr>/Brca1<tm3.1Rjbr>	involves: 129 * C57BL/6	N	22034435
MGI:5494453	M	MP:0001147	small testis	Brca1<tm3.1Rjbr>/Brca1<tm3.1Rjbr>	involves: 129 * C57BL/6	N	22034435
MGI:5494455	M	MP:0005389	reproductive system phenotype	Brca1<tm4.1Rjbr>/Brca1<tm4.1Rjbr>	involves: 129 * C57BL/6	Y	22034435
MGI:5494479	F	MP:0003699	abnormal female reproductive system physiology	Agr2<tm1.1Lex>/Agr2<tm1.1Lex>	involves: 129S5/SvEvBrd * BALB/cJ * C57BL/6	N	23209296
MGI:5494567	M	MP:0005376	homeostasis/metabolism phenotype	Fto<tm1.1Rdc>/Fto<tm1.1Rdc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	Y	23300482
MGI:5494567	M	MP:0010024	increased total body fat amount	Fto<tm1.1Rdc>/Fto<tm1.1Rdc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	23300482
MGI:5494567	M	MP:0003961	decreased lean body mass	Fto<tm1.1Rdc>/Fto<tm1.1Rdc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	23300482
MGI:5494567	M	MP:0010379	decreased respiratory quotient	Fto<tm1.1Rdc>/Fto<tm1.1Rdc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	23300482
MGI:5494567	M	MP:0001262	decreased body weight	Fto<tm1.1Rdc>/Fto<tm1.1Rdc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	23300482
MGI:5494567	M	MP:0008964	decreased carbon dioxide production	Fto<tm1.1Rdc>/Fto<tm1.1Rdc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	23300482
MGI:5494568	M	MP:0003961	decreased lean body mass	Fto<tm1.2Rdc>/Fto<tm1.2Rdc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL	N	23300482
MGI:5494568	M	MP:0010379	decreased respiratory quotient	Fto<tm1.2Rdc>/Fto<tm1.2Rdc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL	N	23300482
MGI:5494568	M	MP:0005376	homeostasis/metabolism phenotype	Fto<tm1.2Rdc>/Fto<tm1.2Rdc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL	Y	23300482
MGI:5494568	M	MP:0001262	decreased body weight	Fto<tm1.2Rdc>/Fto<tm1.2Rdc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL	N	23300482
MGI:5494568	M	MP:0005289	increased oxygen consumption	Fto<tm1.2Rdc>/Fto<tm1.2Rdc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL	N	23300482
MGI:5494568	M	MP:0005292	improved glucose tolerance	Fto<tm1.2Rdc>/Fto<tm1.2Rdc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL	N	23300482
MGI:5494568	M	MP:0011939	increased food intake	Fto<tm1.2Rdc>/Fto<tm1.2Rdc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL	N	23300482
MGI:5494638	M	MP:0003961	decreased lean body mass	Serinc1<Gt(OST454985)Lex>/Serinc1<Gt(OST454985)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:3510987
MGI:5494638	M	MP:0001258	decreased body length	Serinc1<Gt(OST454985)Lex>/Serinc1<Gt(OST454985)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:3510987
MGI:5494638	M	MP:0001262	decreased body weight	Serinc1<Gt(OST454985)Lex>/Serinc1<Gt(OST454985)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:3510987
MGI:5494648	F	MP:0001363	increased anxiety-related response	Tmem43<Gt(OST62799)Lex>/Tmem43<Gt(OST62799)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	MGI:3510987
MGI:5494666	M	MP:0000242	impaired fertilization	Tgm4<tm1a(KOMP)Wtsi>/Tgm4<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	23341775
MGI:5494666	M	MP:0030983	failure of copulatory plug deposition	Tgm4<tm1a(KOMP)Wtsi>/Tgm4<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	23341775
MGI:5494666	M	MP:0003698	abnormal male reproductive system physiology	Tgm4<tm1a(KOMP)Wtsi>/Tgm4<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	23341775
MGI:5494854	M	MP:0008498	decreased IgG3 level	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>	involves: 129P2/OlaHsd * CD-1 * MF1	N	23333305
MGI:5494854	M	MP:0008497	decreased IgG2b level	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>	involves: 129P2/OlaHsd * CD-1 * MF1	N	23333305
MGI:5494854	M	MP:0008495	decreased IgG1 level	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>	involves: 129P2/OlaHsd * CD-1 * MF1	N	23333305
MGI:5494854	M	MP:0005387	immune system phenotype	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>	involves: 129P2/OlaHsd * CD-1 * MF1	Y	23333305
MGI:5494854	M	MP:0010948	abnormal double-strand DNA break repair	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>	involves: 129P2/OlaHsd * CD-1 * MF1	N	23333305
MGI:5494854	M	MP:0004227	increased cellular sensitivity to ionizing radiation	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>	involves: 129P2/OlaHsd * CD-1 * MF1	N	23333305
MGI:5494854	M	MP:0001807	decreased IgA level	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>	involves: 129P2/OlaHsd * CD-1 * MF1	N	23333305
MGI:5494854	M	MP:0011110	preweaning lethality, incomplete penetrance	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>	involves: 129P2/OlaHsd * CD-1 * MF1	N	23333305
MGI:5494854	F	MP:0011100	preweaning lethality, complete penetrance	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>	involves: 129P2/OlaHsd * CD-1 * MF1	N	23333305
MGI:5494854	M	MP:0004816	abnormal class switch recombination	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>	involves: 129P2/OlaHsd * CD-1 * MF1	N	23333305
MGI:5494854	M	MP:0001805	decreased IgG level	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>	involves: 129P2/OlaHsd * CD-1 * MF1	N	23333305
MGI:5494854	M	MP:0002412	increased susceptibility to bacterial infection	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>	involves: 129P2/OlaHsd * CD-1 * MF1	N	23333305
MGI:5494854	M	MP:0008058	abnormal DNA repair	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>	involves: 129P2/OlaHsd * CD-1 * MF1	N	23333305
MGI:5494855	M	MP:0004227	increased cellular sensitivity to ionizing radiation	Rif1<Gt(XT0278)Wtsi>/Rif1<Gt(XT0278)Wtsi>,Trp53bp1<tm1Jc>/Trp53bp1<tm1Jc>	involves: 129P2/OlaHsd * CD-1 * MF1	N	23333305
MGI:5495754	M	MP:0005179	decreased circulating cholesterol level	Fabp6<tm1Lbal>/Fabp6<tm1Lbal>	B6.129-Fabp6<tm1Lbal>	N	23251388
MGI:5495754	M	MP:0002644	decreased circulating triglyceride level	Fabp6<tm1Lbal>/Fabp6<tm1Lbal>	B6.129-Fabp6<tm1Lbal>	N	23251388
MGI:5495754	F	MP:0010026	decreased liver cholesterol level	Fabp6<tm1Lbal>/Fabp6<tm1Lbal>	B6.129-Fabp6<tm1Lbal>	N	23251388
MGI:5495754	F	MP:0003402	decreased liver weight	Fabp6<tm1Lbal>/Fabp6<tm1Lbal>	B6.129-Fabp6<tm1Lbal>	N	23251388
MGI:5495812	F	MP:0001386	abnormal maternal nurturing	Dlg4<tm1.1Tdoi>/Dlg4<tm1.1Tdoi>	B6.Cg-Dlg4<tm1.1Tdoi>	N	23268962
MGI:5495812	F	MP:0003718	maternal effect	Dlg4<tm1.1Tdoi>/Dlg4<tm1.1Tdoi>	B6.Cg-Dlg4<tm1.1Tdoi>	N	23268962
MGI:5495915	F	MP:0001386	abnormal maternal nurturing	Ddc<tm1.1Nwlh>/Ddc<tm1.1Nwlh>	involves: C57BL/6	N	23275025
MGI:5495922	F	MP:0001262	decreased body weight	Nbea<Tg(GH1)240BNec>/Nbea<+>	B6JRj.Cg-Nbea<Tg(GH1)240BNec>	N	23153818
MGI:5495922	F	MP:0003008	enhanced long-term potentiation	Nbea<Tg(GH1)240BNec>/Nbea<+>	B6JRj.Cg-Nbea<Tg(GH1)240BNec>	N	23153818
MGI:5495922	F	MP:0002176	increased brain weight	Nbea<Tg(GH1)240BNec>/Nbea<+>	B6JRj.Cg-Nbea<Tg(GH1)240BNec>	N	23153818
MGI:5495922	F	MP:0009453	enhanced contextual conditioning behavior	Nbea<Tg(GH1)240BNec>/Nbea<+>	B6JRj.Cg-Nbea<Tg(GH1)240BNec>	N	23153818
MGI:5495922	F	MP:0001360	abnormal social investigation	Nbea<Tg(GH1)240BNec>/Nbea<+>	B6JRj.Cg-Nbea<Tg(GH1)240BNec>	N	23153818
MGI:5495922	F	MP:0001441	increased grooming behavior	Nbea<Tg(GH1)240BNec>/Nbea<+>	B6JRj.Cg-Nbea<Tg(GH1)240BNec>	N	23153818
MGI:5495922	F	MP:0002557	abnormal social/conspecific interaction behavior	Nbea<Tg(GH1)240BNec>/Nbea<+>	B6JRj.Cg-Nbea<Tg(GH1)240BNec>	N	23153818
MGI:5495922	F	MP:0001402	decreased locomotor activity	Nbea<Tg(GH1)240BNec>/Nbea<+>	B6JRj.Cg-Nbea<Tg(GH1)240BNec>	N	23153818
MGI:5495922	F	MP:0001463	abnormal spatial learning	Nbea<Tg(GH1)240BNec>/Nbea<+>	B6JRj.Cg-Nbea<Tg(GH1)240BNec>	N	23153818
MGI:5496387	F	MP:0001386	abnormal maternal nurturing	Thpr/Thpr<+>	B6.C3(B6Ei)-A Thpr/GrsrJ	N	MGI:5496129
MGI:5496387	F	MP:0001935	decreased litter size	Thpr/Thpr<+>	B6.C3(B6Ei)-A Thpr/GrsrJ	N	MGI:5496129
MGI:5496669	M	MP:0009289	decreased epididymal fat pad weight	Phf2<tm1.1Yima>/Phf2<tm1.1Yima>	involves: 129 * C57BL/6 * C57BL/6J * SJL	N	23274892
MGI:5496793	F	MP:0001533	abnormal skeleton physiology	Esrra<tm1.1Ics>/Esrra<tm1.1Ics>,Tg(Col1a1-cre)1Kry/0	involves: 129S2/SvPas * FVB	N	23359549
MGI:5496793	F	MP:0000130	abnormal trabecular bone morphology	Esrra<tm1.1Ics>/Esrra<tm1.1Ics>,Tg(Col1a1-cre)1Kry/0	involves: 129S2/SvPas * FVB	N	23359549
MGI:5496794	F	MP:0011939	increased food intake	Gdf15<tm1Breit>/Gdf15<tm1Breit>	B6.Cg-Gdf15<tm1Breit>	N	23468844
MGI:5496794	F	MP:0004890	decreased energy expenditure	Gdf15<tm1Breit>/Gdf15<tm1Breit>	B6.Cg-Gdf15<tm1Breit>	N	23468844
MGI:5496794	F	MP:0003961	decreased lean body mass	Gdf15<tm1Breit>/Gdf15<tm1Breit>	B6.Cg-Gdf15<tm1Breit>	N	23468844
MGI:5496794	F	MP:0008961	abnormal basal metabolism	Gdf15<tm1Breit>/Gdf15<tm1Breit>	B6.Cg-Gdf15<tm1Breit>	N	23468844
MGI:5496794	F	MP:0001402	decreased locomotor activity	Gdf15<tm1Breit>/Gdf15<tm1Breit>	B6.Cg-Gdf15<tm1Breit>	N	23468844
MGI:5496896	F	MP:0000627	abnormal mammary gland morphology	Stk11<tm1Rdp>/Stk11<tm1Rdp>,Tg(MMTV-Erbb2*,-cre)1Mul/0	involves: 129S6/SvEvTac * C57BL/6	N	23451056
MGI:5496896	F	MP:0010308	decreased tumor latency	Stk11<tm1Rdp>/Stk11<tm1Rdp>,Tg(MMTV-Erbb2*,-cre)1Mul/0	involves: 129S6/SvEvTac * C57BL/6	N	23451056
MGI:5496896	F	MP:0010299	increased mammary gland tumor incidence	Stk11<tm1Rdp>/Stk11<tm1Rdp>,Tg(MMTV-Erbb2*,-cre)1Mul/0	involves: 129S6/SvEvTac * C57BL/6	N	23451056
MGI:5496897	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTV-Erbb2*,-cre)1Mul/0	involves: FVB	N	23451056
MGI:5496897	F	MP:0010299	increased mammary gland tumor incidence	Tg(MMTV-Erbb2*,-cre)1Mul/0	involves: FVB	N	23451056
MGI:5496897	F	MP:0010308	decreased tumor latency	Tg(MMTV-Erbb2*,-cre)1Mul/0	involves: FVB	N	23451056
MGI:5497992	M	MP:0004852	decreased testis weight	T(7;18)50H/+	involves: 101/H * C3H/HeH * CBA/H	N	2072976
MGI:5497992	M	MP:0009230	abnormal sperm head morphology	T(7;18)50H/+	involves: 101/H * C3H/HeH * CBA/H	N	2072976
MGI:5497992	M	MP:0001922	reduced male fertility	T(7;18)50H/+	involves: 101/H * C3H/HeH * CBA/H	N	2072976
MGI:5497992	M	MP:0002673	abnormal sperm number	T(7;18)50H/+	involves: 101/H * C3H/HeH * CBA/H	N	2072976
MGI:5497992	F	MP:0001923	reduced female fertility	T(7;18)50H/+	involves: 101/H * C3H/HeH * CBA/H	N	2072976
MGI:5497992	M	MP:0002687	oligozoospermia	T(7;18)50H/+	involves: 101/H * C3H/HeH * CBA/H	N	2072976
MGI:5498652	M	MP:0020011	increased bone mineral density of femur	Tg(Col1a1-FGF2*,-Sapphire)305Mmh/Tg(Col1a1-FGF2*,-Sapphire)305Mmh	involves: FVB/N	N	19056741
MGI:5498652	M	MP:0009347	increased trabecular bone thickness	Tg(Col1a1-FGF2*,-Sapphire)305Mmh/Tg(Col1a1-FGF2*,-Sapphire)305Mmh	involves: FVB/N	N	19056741
MGI:5498652	M	MP:0000062	increased bone mineral density	Tg(Col1a1-FGF2*,-Sapphire)305Mmh/Tg(Col1a1-FGF2*,-Sapphire)305Mmh	involves: FVB/N	N	19056741
MGI:5498652	M	MP:0013623	increased femur compact bone thickness	Tg(Col1a1-FGF2*,-Sapphire)305Mmh/Tg(Col1a1-FGF2*,-Sapphire)305Mmh	involves: FVB/N	N	19056741
MGI:5498652	M	MP:0010867	abnormal bone trabecula morphology	Tg(Col1a1-FGF2*,-Sapphire)305Mmh/Tg(Col1a1-FGF2*,-Sapphire)305Mmh	involves: FVB/N	N	19056741
MGI:5498652	M	MP:0010875	increased bone volume	Tg(Col1a1-FGF2*,-Sapphire)305Mmh/Tg(Col1a1-FGF2*,-Sapphire)305Mmh	involves: FVB/N	N	19056741
MGI:5498652	M	MP:0010123	increased bone mineral content	Tg(Col1a1-FGF2*,-Sapphire)305Mmh/Tg(Col1a1-FGF2*,-Sapphire)305Mmh	involves: FVB/N	N	19056741
MGI:5498652	M	MP:0002397	abnormal bone marrow morphology	Tg(Col1a1-FGF2*,-Sapphire)305Mmh/Tg(Col1a1-FGF2*,-Sapphire)305Mmh	involves: FVB/N	N	19056741
MGI:5498652	M	MP:0001260	increased body weight	Tg(Col1a1-FGF2*,-Sapphire)305Mmh/Tg(Col1a1-FGF2*,-Sapphire)305Mmh	involves: FVB/N	N	19056741
MGI:5498652	M	MP:0003797	abnormal compact bone morphology	Tg(Col1a1-FGF2*,-Sapphire)305Mmh/Tg(Col1a1-FGF2*,-Sapphire)305Mmh	involves: FVB/N	N	19056741
MGI:5498652	M	MP:0010971	abnormal periosteum morphology	Tg(Col1a1-FGF2*,-Sapphire)305Mmh/Tg(Col1a1-FGF2*,-Sapphire)305Mmh	involves: FVB/N	N	19056741
MGI:5498652	M	MP:0021183	increased femoral compact bone area	Tg(Col1a1-FGF2*,-Sapphire)305Mmh/Tg(Col1a1-FGF2*,-Sapphire)305Mmh	involves: FVB/N	N	19056741
MGI:5498672	M	MP:0013623	increased femur compact bone thickness	Tg(Col1a1-FGF2*,-Sapphire)308Mmh/Tg(Col1a1-FGF2*,-Sapphire)308Mmh	involves: FVB/N	N	19056741
MGI:5498672	M	MP:0020011	increased bone mineral density of femur	Tg(Col1a1-FGF2*,-Sapphire)308Mmh/Tg(Col1a1-FGF2*,-Sapphire)308Mmh	involves: FVB/N	N	19056741
MGI:5498672	M	MP:0002397	abnormal bone marrow morphology	Tg(Col1a1-FGF2*,-Sapphire)308Mmh/Tg(Col1a1-FGF2*,-Sapphire)308Mmh	involves: FVB/N	N	19056741
MGI:5498672	M	MP:0021183	increased femoral compact bone area	Tg(Col1a1-FGF2*,-Sapphire)308Mmh/Tg(Col1a1-FGF2*,-Sapphire)308Mmh	involves: FVB/N	N	19056741
MGI:5498672	M	MP:0010971	abnormal periosteum morphology	Tg(Col1a1-FGF2*,-Sapphire)308Mmh/Tg(Col1a1-FGF2*,-Sapphire)308Mmh	involves: FVB/N	N	19056741
MGI:5498672	M	MP:0003797	abnormal compact bone morphology	Tg(Col1a1-FGF2*,-Sapphire)308Mmh/Tg(Col1a1-FGF2*,-Sapphire)308Mmh	involves: FVB/N	N	19056741
MGI:5498672	M	MP:0001260	increased body weight	Tg(Col1a1-FGF2*,-Sapphire)308Mmh/Tg(Col1a1-FGF2*,-Sapphire)308Mmh	involves: FVB/N	N	19056741
MGI:5498672	M	MP:0000062	increased bone mineral density	Tg(Col1a1-FGF2*,-Sapphire)308Mmh/Tg(Col1a1-FGF2*,-Sapphire)308Mmh	involves: FVB/N	N	19056741
MGI:5498672	M	MP:0009347	increased trabecular bone thickness	Tg(Col1a1-FGF2*,-Sapphire)308Mmh/Tg(Col1a1-FGF2*,-Sapphire)308Mmh	involves: FVB/N	N	19056741
MGI:5498672	M	MP:0010875	increased bone volume	Tg(Col1a1-FGF2*,-Sapphire)308Mmh/Tg(Col1a1-FGF2*,-Sapphire)308Mmh	involves: FVB/N	N	19056741
MGI:5498672	M	MP:0010123	increased bone mineral content	Tg(Col1a1-FGF2*,-Sapphire)308Mmh/Tg(Col1a1-FGF2*,-Sapphire)308Mmh	involves: FVB/N	N	19056741
MGI:5498672	M	MP:0010867	abnormal bone trabecula morphology	Tg(Col1a1-FGF2*,-Sapphire)308Mmh/Tg(Col1a1-FGF2*,-Sapphire)308Mmh	involves: FVB/N	N	19056741
MGI:5499170	M	MP:0005389	reproductive system phenotype	Rnf141<tm1Szzh>/Rnf141<tm1Szzh>	involves: 129S1/Sv * C57BL/6J	Y	23196134
MGI:5499210	M	MP:0003631	nervous system phenotype	Hdac6<tm1.1Pmt>/Y	involves: 129P2/OlaHsd * C57BL/6	Y	18180281
MGI:5499210	M	MP:0000062	increased bone mineral density	Hdac6<tm1.1Pmt>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18180281
MGI:5499210	M	MP:0001260	increased body weight	Hdac6<tm1.1Pmt>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18180281
MGI:5499210	M	MP:0001805	decreased IgG level	Hdac6<tm1.1Pmt>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18180281
MGI:5499210	M	MP:0010123	increased bone mineral content	Hdac6<tm1.1Pmt>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18180281
MGI:5499210	M	MP:0005387	immune system phenotype	Hdac6<tm1.1Pmt>/Y	involves: 129P2/OlaHsd * C57BL/6	Y	18180281
MGI:5499210	M	MP:0001806	decreased IgM level	Hdac6<tm1.1Pmt>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18180281
MGI:5499210	M	MP:0005389	reproductive system phenotype	Hdac6<tm1.1Pmt>/Y	involves: 129P2/OlaHsd * C57BL/6	Y	18180281
MGI:5499212	M	MP:0002169	no abnormal phenotype detected	Hdac6<tm1Pmt>/Y	involves: 129P2/OlaHsd * C57BL/6	N	18180281
MGI:5499285	M	MP:0008947	increased neuron number	Hdac6<tm1.1Pmt>/Y,Tg(SOD1*G93A)1Gur/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL	N	23364049
MGI:5499285	M	MP:0010053	decreased grip strength	Hdac6<tm1.1Pmt>/Y,Tg(SOD1*G93A)1Gur/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL	N	23364049
MGI:5499285	M	MP:0005402	abnormal action potential	Hdac6<tm1.1Pmt>/Y,Tg(SOD1*G93A)1Gur/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL	N	23364049
MGI:5499285	M	MP:0010769	abnormal survival	Hdac6<tm1.1Pmt>/Y,Tg(SOD1*G93A)1Gur/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL	N	23364049
MGI:5499285	M	MP:0001052	abnormal innervation pattern to muscle	Hdac6<tm1.1Pmt>/Y,Tg(SOD1*G93A)1Gur/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL	N	23364049
MGI:5499289	M	MP:0002871	albuminuria	Pedm32/Pedm32<+>	involves: C3H * C57BL/6J	N	MGI:4940633
MGI:5499565	F	MP:0002591	decreased mean corpuscular volume	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0003179	thrombocytopenia	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0002398	abnormal bone marrow cell morphology/development	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0004029	spontaneous chromosome breakage	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0010763	abnormal hematopoietic stem cell physiology	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0002417	abnormal megakaryocyte morphology	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0008813	decreased common myeloid progenitor cell number	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0008973	decreased erythroid progenitor cell number	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0002874	decreased hemoglobin content	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0002875	decreased erythrocyte cell number	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0004952	increased spleen weight	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0000245	abnormal erythropoiesis	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0000221	decreased leukocyte cell number	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0000240	extramedullary hematopoiesis	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0001263	weight loss	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0000691	enlarged spleen	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0003795	abnormal bone structure	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0001577	anemia	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0002441	abnormal granulocyte morphology	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499565	F	MP:0005014	increased B cell number	Kdm6a<tm1.1Afst>/Kdm6a<tm1.1Afst>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	N	23365460
MGI:5499566	M	MP:0005397	hematopoietic system phenotype	Kdm6a<tm1.1Afst>/Y,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac	Y	23365460
MGI:5499567	M	MP:0000267	abnormal heart development	Kdm6a<tm1.2Afst>/Y	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	23365460
MGI:5499567	M	MP:0000919	cranioschisis	Kdm6a<tm1.2Afst>/Y	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	23365460
MGI:5499567	M	MP:0011101	prenatal lethality, incomplete penetrance	Kdm6a<tm1.2Afst>/Y	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	23365460
MGI:5499567	M	MP:0003984	embryonic growth retardation	Kdm6a<tm1.2Afst>/Y	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	23365460
MGI:5499567	M	MP:0001672	abnormal embryo development	Kdm6a<tm1.2Afst>/Y	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	23365460
MGI:5499568	F	MP:0000919	cranioschisis	Kdm6a<tm1.2Afst>/Kdm6a<tm1.2Afst>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	23365460
MGI:5499568	F	MP:0003984	embryonic growth retardation	Kdm6a<tm1.2Afst>/Kdm6a<tm1.2Afst>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	23365460
MGI:5499568	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Kdm6a<tm1.2Afst>/Kdm6a<tm1.2Afst>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	23365460
MGI:5499568	F	MP:0000267	abnormal heart development	Kdm6a<tm1.2Afst>/Kdm6a<tm1.2Afst>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	23365460
MGI:5499568	F	MP:0001672	abnormal embryo development	Kdm6a<tm1.2Afst>/Kdm6a<tm1.2Afst>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	N	23365460
MGI:5500063	F	MP:0001923	reduced female fertility	Lin28a<tm1Egm>/Lin28a<tm1Egm>	involves: 129S/SvEv * C57BL/6NTac	N	23378032
MGI:5500063	M	MP:0002687	oligozoospermia	Lin28a<tm1Egm>/Lin28a<tm1Egm>	involves: 129S/SvEv * C57BL/6NTac	N	23378032
MGI:5500063	M	MP:0002780	decreased circulating testosterone level	Lin28a<tm1Egm>/Lin28a<tm1Egm>	involves: 129S/SvEv * C57BL/6NTac	N	23378032
MGI:5500063	F	MP:0004856	decreased ovary weight	Lin28a<tm1Egm>/Lin28a<tm1Egm>	involves: 129S/SvEv * C57BL/6NTac	N	23378032
MGI:5500063	F	MP:0005431	decreased oocyte number	Lin28a<tm1Egm>/Lin28a<tm1Egm>	involves: 129S/SvEv * C57BL/6NTac	N	23378032
MGI:5500063	M	MP:0001922	reduced male fertility	Lin28a<tm1Egm>/Lin28a<tm1Egm>	involves: 129S/SvEv * C57BL/6NTac	N	23378032
MGI:5500063	M	MP:0001380	reduced male mating frequency	Lin28a<tm1Egm>/Lin28a<tm1Egm>	involves: 129S/SvEv * C57BL/6NTac	N	23378032
MGI:5500063	M	MP:0002790	decreased circulating follicle stimulating hormone level	Lin28a<tm1Egm>/Lin28a<tm1Egm>	involves: 129S/SvEv * C57BL/6NTac	N	23378032
MGI:5500063	F	MP:0011121	decreased primordial ovarian follicle number	Lin28a<tm1Egm>/Lin28a<tm1Egm>	involves: 129S/SvEv * C57BL/6NTac	N	23378032
MGI:5500085	M	MP:0005391	vision/eye phenotype	Cacna1a<smrl>/Cacna1a<smrl>	CXB10/HiAJ-Cacna1a<smrl>/GrsrJ	Y	MGI:5499307
MGI:5500085	F	MP:0001935	decreased litter size	Cacna1a<smrl>/Cacna1a<smrl>	CXB10/HiAJ-Cacna1a<smrl>/GrsrJ	N	MGI:5499307
MGI:5500932	M	MP:0011087	neonatal lethality, complete penetrance	Nxf2<tm1.1Jw> Nxf3<tm1.1Jw>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	23677977
MGI:5500934	F	MP:0000951	sporadic seizures	Del(XNxf2-Nxf3)1Jw/+	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5500934	F	MP:0001732	postnatal growth retardation	Del(XNxf2-Nxf3)1Jw/+	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5500934	F	MP:0009358	environmentally induced seizures	Del(XNxf2-Nxf3)1Jw/+	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5500934	F	MP:0001496	audiogenic seizures	Del(XNxf2-Nxf3)1Jw/+	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5500934	F	MP:0001265	decreased body size	Del(XNxf2-Nxf3)1Jw/+	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5500934	F	MP:0021213	complete cleft palate	Del(XNxf2-Nxf3)1Jw/+	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5500934	F	MP:0008770	decreased survivor rate	Del(XNxf2-Nxf3)1Jw/+	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5500934	F	MP:0011086	postnatal lethality, incomplete penetrance	Del(XNxf2-Nxf3)1Jw/+	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5500935	M	MP:0002687	oligozoospermia	Nxf2<tm1.1Jw> Nxf3<tm1.1Jw>/Y,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	23677977
MGI:5500935	M	MP:0001925	male infertility	Nxf2<tm1.1Jw> Nxf3<tm1.1Jw>/Y,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	23677977
MGI:5500935	M	MP:0002686	globozoospermia	Nxf2<tm1.1Jw> Nxf3<tm1.1Jw>/Y,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	23677977
MGI:5500935	M	MP:0001147	small testis	Nxf2<tm1.1Jw> Nxf3<tm1.1Jw>/Y,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	23677977
MGI:5500935	M	MP:0009240	elongated sperm flagellum	Nxf2<tm1.1Jw> Nxf3<tm1.1Jw>/Y,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	23677977
MGI:5500935	M	MP:0008261	arrest of male meiosis	Nxf2<tm1.1Jw> Nxf3<tm1.1Jw>/Y,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	23677977
MGI:5500935	M	MP:0001155	arrest of spermatogenesis	Nxf2<tm1.1Jw> Nxf3<tm1.1Jw>/Y,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	23677977
MGI:5500935	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Nxf2<tm1.1Jw> Nxf3<tm1.1Jw>/Y,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	23677977
MGI:5500935	M	MP:0004852	decreased testis weight	Nxf2<tm1.1Jw> Nxf3<tm1.1Jw>/Y,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	23677977
MGI:5501030	M	MP:0002169	no abnormal phenotype detected	Cul4b<tm1Yxg>/Y	involves: 129X1/SvJ	N	22606329
MGI:5501031	F	MP:0002169	no abnormal phenotype detected	Cul4b<tm1Yxg>/Cul4b<tm1Yxg>	involves: 129X1/SvJ	N	22606329
MGI:5501032	M	MP:0003984	embryonic growth retardation	Cul4b<tm1.1Yxg>/Y	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501032	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Cul4b<tm1.1Yxg>/Y	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501032	M	MP:0013504	increased embryonic tissue cell apoptosis	Cul4b<tm1.1Yxg>/Y	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501032	M	MP:0001698	decreased embryo size	Cul4b<tm1.1Yxg>/Y	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501032	M	MP:0000352	decreased cell proliferation	Cul4b<tm1.1Yxg>/Y	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501032	M	MP:0002582	disorganized extraembryonic tissue	Cul4b<tm1.1Yxg>/Y	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501032	M	MP:0002086	abnormal extraembryonic tissue morphology	Cul4b<tm1.1Yxg>/Y	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501032	M	MP:0002085	abnormal embryonic tissue morphology	Cul4b<tm1.1Yxg>/Y	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0001718	abnormal visceral yolk sac morphology	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0001716	abnormal placenta labyrinth morphology	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0001698	decreased embryo size	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0001262	decreased body weight	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0004266	pale placenta	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0004259	small placenta	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0004201	fetal growth retardation	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0004200	decreased fetal size	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0011527	disorganized placental labyrinth	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0003717	pallor	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0001265	decreased body size	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0001732	postnatal growth retardation	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501033	F	MP:0003984	embryonic growth retardation	Cul4b<tm1.1Yxg>/Cul4b<+>	involves: 129X1/SvJ * FVB/N	N	22606329
MGI:5501506	M	MP:0004153	increased renal tubule apoptosis	Trpv5<Hcalc1>/Trpv5<+>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501506	M	MP:0002135	abnormal kidney morphology	Trpv5<Hcalc1>/Trpv5<+>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501506	M	MP:0002989	small kidney	Trpv5<Hcalc1>/Trpv5<+>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501506	M	MP:0002703	abnormal renal tubule morphology	Trpv5<Hcalc1>/Trpv5<+>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501506	M	MP:0001859	kidney inflammation	Trpv5<Hcalc1>/Trpv5<+>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501506	M	MP:0009640	abnormal renal tubule epithelium morphology	Trpv5<Hcalc1>/Trpv5<+>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501506	M	MP:0003215	renal interstitial fibrosis	Trpv5<Hcalc1>/Trpv5<+>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501506	M	MP:0002705	dilated renal tubule	Trpv5<Hcalc1>/Trpv5<+>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501507	M	MP:0003215	renal interstitial fibrosis	Trpv5<Hcalc1>/Trpv5<Hcalc1>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501507	M	MP:0002989	small kidney	Trpv5<Hcalc1>/Trpv5<Hcalc1>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501507	F	MP:0009346	decreased trabecular bone thickness	Trpv5<Hcalc1>/Trpv5<Hcalc1>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501507	F	MP:0003795	abnormal bone structure	Trpv5<Hcalc1>/Trpv5<Hcalc1>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501507	F	MP:0000198	decreased circulating phosphate level	Trpv5<Hcalc1>/Trpv5<Hcalc1>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501507	M	MP:0002703	abnormal renal tubule morphology	Trpv5<Hcalc1>/Trpv5<Hcalc1>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501507	M	MP:0009640	abnormal renal tubule epithelium morphology	Trpv5<Hcalc1>/Trpv5<Hcalc1>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501507	M	MP:0004153	increased renal tubule apoptosis	Trpv5<Hcalc1>/Trpv5<Hcalc1>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501507	M	MP:0001859	kidney inflammation	Trpv5<Hcalc1>/Trpv5<Hcalc1>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501507	M	MP:0002705	dilated renal tubule	Trpv5<Hcalc1>/Trpv5<Hcalc1>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5501507	M	MP:0002135	abnormal kidney morphology	Trpv5<Hcalc1>/Trpv5<Hcalc1>	involves: C3H/HeH * C57BL/6J	N	23383183
MGI:5502168	M	MP:0002169	no abnormal phenotype detected	Cul4b<tm1.1Pz>/Y	involves: 129 * C57BL/6J	N	22453236
MGI:5502169	F	MP:0002169	no abnormal phenotype detected	Cul4b<tm1.1Pz>/Cul4b<tm1.1Pz>	involves: 129 * C57BL/6J	N	22453236
MGI:5502170	M	MP:0001730	embryonic growth arrest	Cul4b<tm1.1Pz>/Y,Tg(CAG-cre)13Miya/0	involves: 129 * C57BL/6 * C57BL/6J	N	22453236
MGI:5502170	M	MP:0001717	absent ectoplacental cone	Cul4b<tm1.1Pz>/Y,Tg(CAG-cre)13Miya/0	involves: 129 * C57BL/6 * C57BL/6J	N	22453236
MGI:5502170	M	MP:0001693	failure of primitive streak formation	Cul4b<tm1.1Pz>/Y,Tg(CAG-cre)13Miya/0	involves: 129 * C57BL/6 * C57BL/6J	N	22453236
MGI:5502170	M	MP:0001698	decreased embryo size	Cul4b<tm1.1Pz>/Y,Tg(CAG-cre)13Miya/0	involves: 129 * C57BL/6 * C57BL/6J	N	22453236
MGI:5502170	M	MP:0000352	decreased cell proliferation	Cul4b<tm1.1Pz>/Y,Tg(CAG-cre)13Miya/0	involves: 129 * C57BL/6 * C57BL/6J	N	22453236
MGI:5502170	M	MP:0013504	increased embryonic tissue cell apoptosis	Cul4b<tm1.1Pz>/Y,Tg(CAG-cre)13Miya/0	involves: 129 * C57BL/6 * C57BL/6J	N	22453236
MGI:5502170	M	MP:0001675	abnormal ectoderm development	Cul4b<tm1.1Pz>/Y,Tg(CAG-cre)13Miya/0	involves: 129 * C57BL/6 * C57BL/6J	N	22453236
MGI:5502170	M	MP:0001672	abnormal embryo development	Cul4b<tm1.1Pz>/Y,Tg(CAG-cre)13Miya/0	involves: 129 * C57BL/6 * C57BL/6J	N	22453236
MGI:5502170	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Cul4b<tm1.1Pz>/Y,Tg(CAG-cre)13Miya/0	involves: 129 * C57BL/6 * C57BL/6J	N	22453236
MGI:5502171	F	MP:0003229	abnormal vitelline vasculature morphology	Cul4b<tm1.1Pz>/Cul4b<+>,Tg(CAG-cre)13Miya/0	involves: 129 * C57BL/6 * C57BL/6J	N	22453236
MGI:5502171	F	MP:0011099	lethality throughout fetal growth and development, complete penetrance	Cul4b<tm1.1Pz>/Cul4b<+>,Tg(CAG-cre)13Miya/0	involves: 129 * C57BL/6 * C57BL/6J	N	22453236
MGI:5502172	M	MP:0002169	no abnormal phenotype detected	Cul4b<tm1.1Pz>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * C57BL/6J * CBA	N	22453236
MGI:5502173	F	MP:0010768	mortality/aging	Cul4b<tm1.1Pz>/Cul4b<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * C57BL/6J * CBA	Y	22453236
MGI:5502320	M	MP:0011940	decreased food intake	Plin2<tm1.1Asg>/Plin2<tm1.1Asg>	B6.129S2(Cg)-Plin2<tm1.1Asg>	N	23402988
MGI:5502320	F	MP:0008779	abnormal maternal behavior	Plin2<tm1.1Asg>/Plin2<tm1.1Asg>	B6.129S2(Cg)-Plin2<tm1.1Asg>	N	23402988
MGI:5502351	M	MP:0002687	oligozoospermia	Nabp2<tm1.1Kkha>/Nabp2<tm1.1Kkha>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	23408915
MGI:5502351	M	MP:0001922	reduced male fertility	Nabp2<tm1.1Kkha>/Nabp2<tm1.1Kkha>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	23408915
MGI:5502351	M	MP:0006362	abnormal male germ cell morphology	Nabp2<tm1.1Kkha>/Nabp2<tm1.1Kkha>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	23408915
MGI:5502351	M	MP:0001935	decreased litter size	Nabp2<tm1.1Kkha>/Nabp2<tm1.1Kkha>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	23408915
MGI:5502351	M	MP:0004852	decreased testis weight	Nabp2<tm1.1Kkha>/Nabp2<tm1.1Kkha>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	23408915
MGI:5502351	M	MP:0013600	testis degeneration	Nabp2<tm1.1Kkha>/Nabp2<tm1.1Kkha>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	23408915
MGI:5502351	F	MP:0005389	reproductive system phenotype	Nabp2<tm1.1Kkha>/Nabp2<tm1.1Kkha>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	Y	23408915
MGI:5502351	M	MP:0001147	small testis	Nabp2<tm1.1Kkha>/Nabp2<tm1.1Kkha>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	23408915
MGI:5502351	M	MP:0008280	abnormal male germ cell apoptosis	Nabp2<tm1.1Kkha>/Nabp2<tm1.1Kkha>,Gt(ROSA)26Sor<tm9(cre/ESR1)Arte>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac	N	23408915
MGI:5502424	M	MP:0000135	decreased compact bone thickness	Pkd1<tm2Ggg>/Pkd1<+>,Tg(Col1a1-cre)1Bek/0	involves: 129S4/SvJae * CD-1	N	23029375
MGI:5502424	M	MP:0010879	decreased trabecular bone volume	Pkd1<tm2Ggg>/Pkd1<+>,Tg(Col1a1-cre)1Bek/0	involves: 129S4/SvJae * CD-1	N	23029375
MGI:5502687	M	MP:0009283	decreased gonadal fat pad weight	Ar<tm1Verh>/Y,Tg(Fabp4-cre)1Rev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22415878
MGI:5502687	M	MP:0002079	increased circulating insulin level	Ar<tm1Verh>/Y,Tg(Fabp4-cre)1Rev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22415878
MGI:5502687	M	MP:0009294	increased interscapular fat pad weight	Ar<tm1Verh>/Y,Tg(Fabp4-cre)1Rev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22415878
MGI:5502687	M	MP:0010045	increased omental fat pad weight	Ar<tm1Verh>/Y,Tg(Fabp4-cre)1Rev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22415878
MGI:5502687	M	MP:0005452	abnormal adipose tissue amount	Ar<tm1Verh>/Y,Tg(Fabp4-cre)1Rev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22415878
MGI:5502687	M	MP:0005331	insulin resistance	Ar<tm1Verh>/Y,Tg(Fabp4-cre)1Rev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22415878
MGI:5502687	M	MP:0010182	decreased susceptibility to weight gain	Ar<tm1Verh>/Y,Tg(Fabp4-cre)1Rev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22415878
MGI:5502687	M	MP:0001552	increased circulating triglyceride level	Ar<tm1Verh>/Y,Tg(Fabp4-cre)1Rev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22415878
MGI:5502687	M	MP:0009298	increased mesenteric fat pad weight	Ar<tm1Verh>/Y,Tg(Fabp4-cre)1Rev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22415878
MGI:5502687	M	MP:0005293	impaired glucose tolerance	Ar<tm1Verh>/Y,Tg(Fabp4-cre)1Rev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22415878
MGI:5502687	M	MP:0000005	increased brown adipose tissue amount	Ar<tm1Verh>/Y,Tg(Fabp4-cre)1Rev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22415878
MGI:5502687	M	MP:0001559	hyperglycemia	Ar<tm1Verh>/Y,Tg(Fabp4-cre)1Rev/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22415878
MGI:5502765	M	MP:0010084	abnormal long lived plasma cell morphology	Sh2d1a<tm1Pls>/Y	involves: 129S6/SvEvTac	N	20153220
MGI:5502765	M	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Sh2d1a<tm1Pls>/Y	involves: 129S6/SvEvTac	N	20153220
MGI:5502765	M	MP:0008036	abnormal NK T cell morphology	Sh2d1a<tm1Pls>/Y	involves: 129S6/SvEvTac	N	23430111
MGI:5502765	M	MP:0005078	abnormal cytotoxic T cell physiology	Sh2d1a<tm1Pls>/Y	involves: 129S6/SvEvTac	N	22683123
MGI:5502765	M	MP:0001805	decreased IgG level	Sh2d1a<tm1Pls>/Y	involves: 129S6/SvEvTac	N	20153220
MGI:5502765	M	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology	Sh2d1a<tm1Pls>/Y	involves: 129S6/SvEvTac	N	20153220
MGI:5502765	M	MP:0009058	decreased interleukin-21 secretion	Sh2d1a<tm1Pls>/Y	involves: 129S6/SvEvTac	N	20153220
MGI:5502766	M	MP:0008567	decreased interferon-gamma secretion	Sh2d1a<tm1.1Knic>/Y,Gt(ROSA)26Sor<tm1(EYFP)Cos>/Gt(ROSA)26Sor<+>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * 129X1/SvJ * C57BL/6	N	23430111
MGI:5502766	M	MP:0008042	abnormal NK T cell physiology	Sh2d1a<tm1.1Knic>/Y,Gt(ROSA)26Sor<tm1(EYFP)Cos>/Gt(ROSA)26Sor<+>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * 129X1/SvJ * C57BL/6	N	23430111
MGI:5502766	M	MP:0005387	immune system phenotype	Sh2d1a<tm1.1Knic>/Y,Gt(ROSA)26Sor<tm1(EYFP)Cos>/Gt(ROSA)26Sor<+>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * 129X1/SvJ * C57BL/6	Y	23430111
MGI:5502766	M	MP:0008603	decreased circulating interleukin-4 level	Sh2d1a<tm1.1Knic>/Y,Gt(ROSA)26Sor<tm1(EYFP)Cos>/Gt(ROSA)26Sor<+>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * 129X1/SvJ * C57BL/6	N	23430111
MGI:5504390	F	MP:0002727	decreased circulating insulin level	Met<tm1Sst>/Met<tm1Sst>,Tg(Pdx1-cre)89.1Dam/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	22427375
MGI:5504390	F	MP:0005559	increased circulating glucose level	Met<tm1Sst>/Met<tm1Sst>,Tg(Pdx1-cre)89.1Dam/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	22427375
MGI:5504390	F	MP:0005215	abnormal pancreatic islet morphology	Met<tm1Sst>/Met<tm1Sst>,Tg(Pdx1-cre)89.1Dam/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	22427375
MGI:5504390	F	MP:0003059	decreased insulin secretion	Met<tm1Sst>/Met<tm1Sst>,Tg(Pdx1-cre)89.1Dam/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	22427375
MGI:5504390	F	MP:0005293	impaired glucose tolerance	Met<tm1Sst>/Met<tm1Sst>,Tg(Pdx1-cre)89.1Dam/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	22427375
MGI:5504390	F	MP:0009114	decreased pancreatic beta cell mass	Met<tm1Sst>/Met<tm1Sst>,Tg(Pdx1-cre)89.1Dam/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	22427375
MGI:5504390	F	MP:0011820	decreased pancreatic beta cell proliferation	Met<tm1Sst>/Met<tm1Sst>,Tg(Pdx1-cre)89.1Dam/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	22427375
MGI:5504390	F	MP:0003562	abnormal pancreatic beta cell physiology	Met<tm1Sst>/Met<tm1Sst>,Tg(Pdx1-cre)89.1Dam/0	involves: 129P2/OlaHsd * C57BL/6 * CBA	N	22427375
MGI:5504442	M	MP:0001402	decreased locomotor activity	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0014143	decreased body fat mass	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0005289	increased oxygen consumption	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0004889	increased energy expenditure	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0001262	decreased body weight	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0010379	decreased respiratory quotient	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0010724	thick interventricular septum	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0000266	abnormal heart morphology	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0002972	abnormal cardiac muscle contractility	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0002644	decreased circulating triglyceride level	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0002078	abnormal glucose homeostasis	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0003921	abnormal heart left ventricle morphology	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0001559	hyperglycemia	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0031414	decreased skeletal muscle triglyceride level	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0002727	decreased circulating insulin level	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0009356	decreased liver triglyceride level	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0005331	insulin resistance	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0030022	decreased muscle cell glucose uptake	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0030016	increased adipocyte glucose uptake	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0030017	decreased adipocyte glucose uptake	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0011939	increased food intake	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0008963	increased carbon dioxide production	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504442	M	MP:0002625	heart left ventricle hypertrophy	Ins2<Akita>/?	involves: C57BL/6NSlc	N	17911348
MGI:5504450	M	MP:0001925	male infertility	Sox3<tm1Pqt>/Y	chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	23505376
MGI:5504450	M	MP:0009463	abnormal pituitary infundibular stalk morphology	Sox3<tm1Pqt>/Y	chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	23505376
MGI:5504450	M	MP:0013337	abnormal adenohypophysis development	Sox3<tm1Pqt>/Y	chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	23505376
MGI:5504450	M	MP:0014198	absent pituitary infundibular stalk	Sox3<tm1Pqt>/Y	chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	23505376
MGI:5504450	M	MP:0005380	embryo phenotype	Sox3<tm1Pqt>/Y	chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	Y	23505376
MGI:5504450	M	MP:0005384	cellular phenotype	Sox3<tm1Pqt>/Y	chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	Y	23505376
MGI:5505394	F	MP:0002777	absent ovarian follicles	Mad2l2<tm1Ymu>/Mad2l2<tm1Ymu>	involves: 129 * C57BL/6J	N	23463509
MGI:5505394	F	MP:0001127	small ovary	Mad2l2<tm1Ymu>/Mad2l2<tm1Ymu>	involves: 129 * C57BL/6J	N	23463509
MGI:5505394	M	MP:0001262	decreased body weight	Mad2l2<tm1Ymu>/Mad2l2<tm1Ymu>	involves: 129 * C57BL/6J	N	23463509
MGI:5505394	F	MP:0004833	ovary atrophy	Mad2l2<tm1Ymu>/Mad2l2<tm1Ymu>	involves: 129 * C57BL/6J	N	23463509
MGI:5505394	M	MP:0001147	small testis	Mad2l2<tm1Ymu>/Mad2l2<tm1Ymu>	involves: 129 * C57BL/6J	N	23463509
MGI:5505394	F	MP:0001931	abnormal oogenesis	Mad2l2<tm1Ymu>/Mad2l2<tm1Ymu>	involves: 129 * C57BL/6J	N	23463509
MGI:5505394	M	MP:0004852	decreased testis weight	Mad2l2<tm1Ymu>/Mad2l2<tm1Ymu>	involves: 129 * C57BL/6J	N	23463509
MGI:5505394	M	MP:0001156	abnormal spermatogenesis	Mad2l2<tm1Ymu>/Mad2l2<tm1Ymu>	involves: 129 * C57BL/6J	N	23463509
MGI:5505394	M	MP:0001925	male infertility	Mad2l2<tm1Ymu>/Mad2l2<tm1Ymu>	involves: 129 * C57BL/6J	N	23463509
MGI:5505394	M	MP:0005159	azoospermia	Mad2l2<tm1Ymu>/Mad2l2<tm1Ymu>	involves: 129 * C57BL/6J	N	23463509
MGI:5505394	M	MP:0001154	seminiferous tubule degeneration	Mad2l2<tm1Ymu>/Mad2l2<tm1Ymu>	involves: 129 * C57BL/6J	N	23463509
MGI:5505394	F	MP:0001926	female infertility	Mad2l2<tm1Ymu>/Mad2l2<tm1Ymu>	involves: 129 * C57BL/6J	N	23463509
MGI:5505897	M	MP:0001935	decreased litter size	Khdrbs3<tm1.2Dell>/Khdrbs3<tm1.2Dell>	involves: 129S2/SvPas * C57BL/6	N	23637638
MGI:5505897	M	MP:0005389	reproductive system phenotype	Khdrbs3<tm1.2Dell>/Khdrbs3<tm1.2Dell>	involves: 129S2/SvPas * C57BL/6	Y	23637638
MGI:5505899	M	MP:0006362	abnormal male germ cell morphology	Rnf168<Gt(156B6)Cmhd>/Rnf168<Gt(156B6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21552324
MGI:5505899	M	MP:0003205	testicular atrophy	Rnf168<Gt(156B6)Cmhd>/Rnf168<Gt(156B6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21552324
MGI:5505899	M	MP:0004901	decreased male germ cell number	Rnf168<Gt(156B6)Cmhd>/Rnf168<Gt(156B6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21552324
MGI:5505899	M	MP:0001147	small testis	Rnf168<Gt(156B6)Cmhd>/Rnf168<Gt(156B6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21552324
MGI:5505899	M	MP:0001922	reduced male fertility	Rnf168<Gt(156B6)Cmhd>/Rnf168<Gt(156B6)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21552324
MGI:5505901	M	MP:0003205	testicular atrophy	Rnf168<Gt(405F11)Cmhd>/Rnf168<Gt(405F11)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21552324
MGI:5505901	M	MP:0004901	decreased male germ cell number	Rnf168<Gt(405F11)Cmhd>/Rnf168<Gt(405F11)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21552324
MGI:5505901	M	MP:0001147	small testis	Rnf168<Gt(405F11)Cmhd>/Rnf168<Gt(405F11)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21552324
MGI:5505901	M	MP:0001922	reduced male fertility	Rnf168<Gt(405F11)Cmhd>/Rnf168<Gt(405F11)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21552324
MGI:5505901	M	MP:0006362	abnormal male germ cell morphology	Rnf168<Gt(405F11)Cmhd>/Rnf168<Gt(405F11)Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21552324
MGI:5506633	F	MP:0001126	abnormal ovary morphology	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5506633	M	MP:0001156	abnormal spermatogenesis	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5506633	M	MP:0001940	testis hypoplasia	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5506633	M	MP:0002216	abnormal seminiferous tubule morphology	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5506633	F	MP:0008871	abnormal ovarian follicle number	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5506633	F	MP:0001926	female infertility	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5506633	M	MP:0001146	abnormal testis morphology	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5506633	M	MP:0001925	male infertility	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5506633	F	MP:0001127	small ovary	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5506633	F	MP:0001931	abnormal oogenesis	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5506633	F	MP:0002680	decreased corpora lutea number	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5506633	M	MP:0008261	arrest of male meiosis	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5506633	M	MP:0001147	small testis	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5506633	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Hfm1<Gt(OST347241)Lex>/Hfm1<Gt(OST347241)Lex>	involves: 129S5/SvEvBrd * C57BL/6 * SJL	N	23555294
MGI:5507863	F	MP:0009397	increased trophoblast giant cell number	Kdm6a<tm1b(EUCOMM)Jae>/Kdm6a<tm1b(EUCOMM)Jae>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	22826230
MGI:5507863	F	MP:0002084	abnormal developmental patterning	Kdm6a<tm1b(EUCOMM)Jae>/Kdm6a<tm1b(EUCOMM)Jae>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	22826230
MGI:5507863	F	MP:0004180	failure of initiation of embryo turning	Kdm6a<tm1b(EUCOMM)Jae>/Kdm6a<tm1b(EUCOMM)Jae>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	22826230
MGI:5507863	F	MP:0003794	delayed somite formation	Kdm6a<tm1b(EUCOMM)Jae>/Kdm6a<tm1b(EUCOMM)Jae>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	22826230
MGI:5507863	F	MP:0000267	abnormal heart development	Kdm6a<tm1b(EUCOMM)Jae>/Kdm6a<tm1b(EUCOMM)Jae>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	22826230
MGI:5507863	F	MP:0003720	abnormal neural tube closure	Kdm6a<tm1b(EUCOMM)Jae>/Kdm6a<tm1b(EUCOMM)Jae>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	22826230
MGI:5507863	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Kdm6a<tm1b(EUCOMM)Jae>/Kdm6a<tm1b(EUCOMM)Jae>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	22826230
MGI:5507864	M	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Kdm6a<tm1b(EUCOMM)Jae>/Y	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	22826230
MGI:5507864	M	MP:0009674	decreased birth weight	Kdm6a<tm1b(EUCOMM)Jae>/Y	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	22826230
MGI:5507864	M	MP:0001732	postnatal growth retardation	Kdm6a<tm1b(EUCOMM)Jae>/Y	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	22826230
MGI:5507864	M	MP:0005389	reproductive system phenotype	Kdm6a<tm1b(EUCOMM)Jae>/Y	involves: 129S4/SvJae * C57BL/6 * FVB/N	Y	22826230
MGI:5508227	M	MP:0009281	abnormal hyperactivated sperm motility	Tex101<tm1Osb>/Tex101<tm1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/Tg(CAG-EGFP,Acr-EGFP)2Osb	involves: C57BL/6NSlc	N	23633567
MGI:5508227	M	MP:0001925	male infertility	Tex101<tm1Osb>/Tex101<tm1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/Tg(CAG-EGFP,Acr-EGFP)2Osb	involves: C57BL/6NSlc	N	23633567
MGI:5508227	M	MP:0031012	impaired sperm migration in female genital tract	Tex101<tm1Osb>/Tex101<tm1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/Tg(CAG-EGFP,Acr-EGFP)2Osb	involves: C57BL/6NSlc	N	23633567
MGI:5508227	M	MP:0013287	abnormal acrosome reaction	Tex101<tm1Osb>/Tex101<tm1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/Tg(CAG-EGFP,Acr-EGFP)2Osb	involves: C57BL/6NSlc	N	23633567
MGI:5508227	M	MP:0005386	behavior/neurological phenotype	Tex101<tm1Osb>/Tex101<tm1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/Tg(CAG-EGFP,Acr-EGFP)2Osb	involves: C57BL/6NSlc	Y	23633567
MGI:5508227	M	MP:0030978	impaired binding of sperm to zona pellucida	Tex101<tm1Osb>/Tex101<tm1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/Tg(CAG-EGFP,Acr-EGFP)2Osb	involves: C57BL/6NSlc	N	23633567
MGI:5508227	M	MP:0005389	reproductive system phenotype	Tex101<tm1Osb>/Tex101<tm1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/Tg(CAG-EGFP,Acr-EGFP)2Osb	involves: C57BL/6NSlc	Y	23633567
MGI:5508535	F	MP:0002566	abnormal sexual interaction	Del(2Hoxd1-Hoxd9)63Ddu/+	involves: C57BL/6 * CBA	N	22863319
MGI:5508535	F	MP:0011988	increased mating frequency	Del(2Hoxd1-Hoxd9)63Ddu/+	involves: C57BL/6 * CBA	N	22863319
MGI:5508810	M	MP:0009745	abnormal behavioral response to xenobiotic	Gsk3a<tm1Dral>/Gsk3a<tm1Dral>,Gsk3b<tm1Dral>/Gsk3b<tm1Dral>	involves: 129P2/OlaHsd	N	20357757
MGI:5508810	M	MP:0001399	hyperactivity	Gsk3a<tm1Dral>/Gsk3a<tm1Dral>,Gsk3b<tm1Dral>/Gsk3b<tm1Dral>	involves: 129P2/OlaHsd	N	20357757
MGI:5508810	M	MP:0001415	increased exploration in new environment	Gsk3a<tm1Dral>/Gsk3a<tm1Dral>,Gsk3b<tm1Dral>/Gsk3b<tm1Dral>	involves: 129P2/OlaHsd	N	20357757
MGI:5508810	M	MP:0009453	enhanced contextual conditioning behavior	Gsk3a<tm1Dral>/Gsk3a<tm1Dral>,Gsk3b<tm1Dral>/Gsk3b<tm1Dral>	involves: 129P2/OlaHsd	N	20357757
MGI:5508810	M	MP:0001745	increased circulating corticosterone level	Gsk3a<tm1Dral>/Gsk3a<tm1Dral>,Gsk3b<tm1Dral>/Gsk3b<tm1Dral>	involves: 129P2/OlaHsd	N	20357757
MGI:5508810	M	MP:0008596	increased circulating interleukin-6 level	Gsk3a<tm1Dral>/Gsk3a<tm1Dral>,Gsk3b<tm1Dral>/Gsk3b<tm1Dral>	involves: 129P2/OlaHsd	N	20357757
MGI:5508810	M	MP:0003064	decreased coping response	Gsk3a<tm1Dral>/Gsk3a<tm1Dral>,Gsk3b<tm1Dral>/Gsk3b<tm1Dral>	involves: 129P2/OlaHsd	N	20357757
MGI:5508810	M	MP:0001363	increased anxiety-related response	Gsk3a<tm1Dral>/Gsk3a<tm1Dral>,Gsk3b<tm1Dral>/Gsk3b<tm1Dral>	involves: 129P2/OlaHsd	N	20357757
MGI:5508810	M	MP:0002797	increased thigmotaxis	Gsk3a<tm1Dral>/Gsk3a<tm1Dral>,Gsk3b<tm1Dral>/Gsk3b<tm1Dral>	involves: 129P2/OlaHsd	N	20357757
MGI:5508810	M	MP:0001898	abnormal long-term depression	Gsk3a<tm1Dral>/Gsk3a<tm1Dral>,Gsk3b<tm1Dral>/Gsk3b<tm1Dral>	involves: 129P2/OlaHsd	N	20357757
MGI:5508810	M	MP:0009456	impaired cued conditioning behavior	Gsk3a<tm1Dral>/Gsk3a<tm1Dral>,Gsk3b<tm1Dral>/Gsk3b<tm1Dral>	involves: 129P2/OlaHsd	N	20357757
MGI:5509039	M	MP:0005621	abnormal cell physiology	Zbtb32<Gt(IST12443F7)Tigm>/Zbtb32<Gt(IST12443F7)Tigm>	involves: C57BL/6N	N	22965116
MGI:5509044	F	MP:0001938	delayed sexual maturation	Cenpj<tm1a(EUCOMM)Wtsi>/Cenpj<tm1a(EUCOMM)Wtsi>	B6Brd;B6N-Tyr<c-Brd> Cenpj<tm1a(EUCOMM)Wtsi>/Wtsi	N	23166506
MGI:5509299	F	MP:0001405	impaired coordination	Tg(SNCA*E46K)3Elan/?	involves: C57BL/6 * SJL	N	MGI:5509204
MGI:5510773	M	MP:0001146	abnormal testis morphology	Scara5<tm1Ktry>/Scara5<tm1Ktry>	B6N.129X1-Scara5<tm1Ktry>	N	23499552
MGI:5510773	M	MP:0001922	reduced male fertility	Scara5<tm1Ktry>/Scara5<tm1Ktry>	B6N.129X1-Scara5<tm1Ktry>	N	23499552
MGI:5510816	M	MP:0006418	abnormal testis cord formation	m6Anu/m6Anu	involves: C3H/HeH * C57BL/6JAnu	N	23469164
MGI:5510816	M	MP:0006419	disorganized testis cords	m6Anu/m6Anu	involves: C3H/HeH * C57BL/6JAnu	N	23469164
MGI:5510816	M	MP:0001147	small testis	m6Anu/m6Anu	involves: C3H/HeH * C57BL/6JAnu	N	23469164
MGI:5510818	M	MP:0006418	abnormal testis cord formation	m7Anu/m7Anu	involves: C3H/HeH * C57BL/6JAnu	N	23469164
MGI:5510818	M	MP:0001147	small testis	m7Anu/m7Anu	involves: C3H/HeH * C57BL/6JAnu	N	23469164
MGI:5510994	M	MP:0001409	increased stereotypic behavior	Tg(ACTB-Eif4e)#Ppp/?	B6.Cg-Tg(ACTB-Eif4e)#Ppp	N	23263185
MGI:5510994	M	MP:0001399	hyperactivity	Tg(ACTB-Eif4e)#Ppp/?	B6.Cg-Tg(ACTB-Eif4e)#Ppp	N	23263185
MGI:5510994	M	MP:0020340	abnormal inhibitory learning	Tg(ACTB-Eif4e)#Ppp/?	B6.Cg-Tg(ACTB-Eif4e)#Ppp	N	23263185
MGI:5510994	M	MP:0001360	abnormal social investigation	Tg(ACTB-Eif4e)#Ppp/?	B6.Cg-Tg(ACTB-Eif4e)#Ppp	N	23263185
MGI:5510994	M	MP:0001441	increased grooming behavior	Tg(ACTB-Eif4e)#Ppp/?	B6.Cg-Tg(ACTB-Eif4e)#Ppp	N	23263185
MGI:5511050	F	MP:0012075	impaired mammary gland growth during pregnancy	Lbh<tm1.2Kbri>/Lbh<tm1.2Kbri>	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23495064
MGI:5511050	F	MP:0006271	abnormal involution of the mammary gland	Lbh<tm1.2Kbri>/Lbh<tm1.2Kbri>	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23495064
MGI:5511050	F	MP:0006270	abnormal mammary gland growth during lactation	Lbh<tm1.2Kbri>/Lbh<tm1.2Kbri>	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23495064
MGI:5511050	F	MP:0009506	abnormal mammary gland alveolus morphology	Lbh<tm1.2Kbri>/Lbh<tm1.2Kbri>	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23495064
MGI:5511050	F	MP:0003344	mammary gland hypoplasia	Lbh<tm1.2Kbri>/Lbh<tm1.2Kbri>	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23495064
MGI:5511050	F	MP:0001935	decreased litter size	Lbh<tm1.2Kbri>/Lbh<tm1.2Kbri>	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23495064
MGI:5511050	F	MP:0000628	abnormal mammary gland development	Lbh<tm1.2Kbri>/Lbh<tm1.2Kbri>	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23495064
MGI:5511053	M	MP:0001146	abnormal testis morphology	Golga3<repro27>/Golga3<repro27>	C3Fe.B6-Golga3<repro27>	N	23495255
MGI:5512669	M	MP:0003153	early eyelid opening	Gpr37l1<tm1.2Gtva>/Gpr37l1<tm1.2Gtva>	involves: 129S/SvEv * BALB/c * C57BL/6J	N	24062445
MGI:5512669	M	MP:0003313	abnormal locomotor activation	Gpr37l1<tm1.2Gtva>/Gpr37l1<tm1.2Gtva>	involves: 129S/SvEv * BALB/c * C57BL/6J	N	24062445
MGI:5512669	M	MP:0003858	enhanced coordination	Gpr37l1<tm1.2Gtva>/Gpr37l1<tm1.2Gtva>	involves: 129S/SvEv * BALB/c * C57BL/6J	N	24062445
MGI:5512699	M	MP:0001469	abnormal contextual conditioning behavior	Tg(Prnp-MAPT*P301S)PS19Vle/0	B6.Cg-Tg(Prnp-MAPT*P301S)PS19Vle	N	21698260
MGI:5512699	M	MP:0002574	increased vertical activity	Tg(Prnp-MAPT*P301S)PS19Vle/0	B6.Cg-Tg(Prnp-MAPT*P301S)PS19Vle	N	21698260
MGI:5512699	M	MP:0003998	decreased thermal nociceptive threshold	Tg(Prnp-MAPT*P301S)PS19Vle/0	B6.Cg-Tg(Prnp-MAPT*P301S)PS19Vle	N	21698260
MGI:5512699	M	MP:0002572	abnormal emotion/affect behavior	Tg(Prnp-MAPT*P301S)PS19Vle/0	B6.Cg-Tg(Prnp-MAPT*P301S)PS19Vle	N	21698260
MGI:5512699	M	MP:0009141	increased prepulse inhibition	Tg(Prnp-MAPT*P301S)PS19Vle/0	B6.Cg-Tg(Prnp-MAPT*P301S)PS19Vle	N	21698260
MGI:5512699	M	MP:0001360	abnormal social investigation	Tg(Prnp-MAPT*P301S)PS19Vle/0	B6.Cg-Tg(Prnp-MAPT*P301S)PS19Vle	N	21698260
MGI:5512699	M	MP:0031391	increased locomotor activity	Tg(Prnp-MAPT*P301S)PS19Vle/0	B6.Cg-Tg(Prnp-MAPT*P301S)PS19Vle	N	21698260
MGI:5512699	M	MP:0004250	tau protein deposits	Tg(Prnp-MAPT*P301S)PS19Vle/0	B6.Cg-Tg(Prnp-MAPT*P301S)PS19Vle	N	21698260
MGI:5512699	M	MP:0001364	decreased anxiety-related response	Tg(Prnp-MAPT*P301S)PS19Vle/0	B6.Cg-Tg(Prnp-MAPT*P301S)PS19Vle	N	21698260
MGI:5512699	M	MP:0004924	abnormal behavior	Tg(Prnp-MAPT*P301S)PS19Vle/0	B6.Cg-Tg(Prnp-MAPT*P301S)PS19Vle	N	21698260
MGI:5512850	F	MP:0001935	decreased litter size	Ywhae<tm1Awb>/Ywhae<+>	involves: 129S6/SvEvTac	N	23071090
MGI:5512992	M	MP:0020470	shortened circadian behavior period	Maged1<tm1Xgao>/Y	B6.Cg-Maged1<tm1Xgao>	N	20300063
MGI:5512992	M	MP:0020476	abnormal circardian behavior entrainment	Maged1<tm1Xgao>/Y	B6.Cg-Maged1<tm1Xgao>	N	20300063
MGI:5512992	M	MP:0020467	abnormal circadian behavior	Maged1<tm1Xgao>/Y	B6.Cg-Maged1<tm1Xgao>	N	20300063
MGI:5512993	F	MP:0020470	shortened circadian behavior period	Maged1<tm1Xgao>/Maged1<tm1Xgao>	B6.Cg-Maged1<tm1Xgao>	N	20300063
MGI:5512993	F	MP:0020476	abnormal circardian behavior entrainment	Maged1<tm1Xgao>/Maged1<tm1Xgao>	B6.Cg-Maged1<tm1Xgao>	N	20300063
MGI:5512993	F	MP:0020467	abnormal circadian behavior	Maged1<tm1Xgao>/Maged1<tm1Xgao>	B6.Cg-Maged1<tm1Xgao>	N	20300063
MGI:5512994	F	MP:0020470	shortened circadian behavior period	Maged1<tm1Xgao>/Maged1<+>	B6.Cg-Maged1<tm1Xgao>	N	20300063
MGI:5514055	F	MP:0000067	osteopetrosis	Ostm1<om>/Ostm1<om>	C3HeB/FeJ-Ostm1<om>	N	23160729
MGI:5514182	M	MP:0004502	decreased incidence of tumors by chemical induction	Mmp1a<tm1Otin>/Mmp1a<tm1Otin>	involves: 129P2/OlaHsd * C57BL/6J	N	23548910
MGI:5514182	M	MP:0003447	decreased tumor growth/size	Mmp1a<tm1Otin>/Mmp1a<tm1Otin>	involves: 129P2/OlaHsd * C57BL/6J	N	23548910
MGI:5514254	M	MP:0010333	abnormal circulating apolipoprotein E level	Osbpl8<Gt(DD0748)Wtsi>/Osbpl8<Gt(DD0748)Wtsi>	B6.129P2-Osbpl8<Gt(DD0748)Wtsi>	N	23554939
MGI:5514261	M	MP:0005621	abnormal cell physiology	Ttll5<tm1.1N>/Ttll5<tm1.1N>	involves: 129S6/SvEvTac * C57BL/6NTac * FVB/N	N	23558686
MGI:5514261	M	MP:0001922	reduced male fertility	Ttll5<tm1.1N>/Ttll5<tm1.1N>	involves: 129S6/SvEvTac * C57BL/6NTac * FVB/N	N	23558686
MGI:5514261	M	MP:0009238	coiled sperm flagellum	Ttll5<tm1.1N>/Ttll5<tm1.1N>	involves: 129S6/SvEvTac * C57BL/6NTac * FVB/N	N	23558686
MGI:5514261	M	MP:0001935	decreased litter size	Ttll5<tm1.1N>/Ttll5<tm1.1N>	involves: 129S6/SvEvTac * C57BL/6NTac * FVB/N	N	23558686
MGI:5514261	M	MP:0009647	decreased fertilization frequency	Ttll5<tm1.1N>/Ttll5<tm1.1N>	involves: 129S6/SvEvTac * C57BL/6NTac * FVB/N	N	23558686
MGI:5514261	M	MP:0005578	teratozoospermia	Ttll5<tm1.1N>/Ttll5<tm1.1N>	involves: 129S6/SvEvTac * C57BL/6NTac * FVB/N	N	23558686
MGI:5514261	M	MP:0009838	abnormal sperm axoneme morphology	Ttll5<tm1.1N>/Ttll5<tm1.1N>	involves: 129S6/SvEvTac * C57BL/6NTac * FVB/N	N	23558686
MGI:5514261	M	MP:0002675	asthenozoospermia	Ttll5<tm1.1N>/Ttll5<tm1.1N>	involves: 129S6/SvEvTac * C57BL/6NTac * FVB/N	N	23558686
MGI:5514277	M	MP:0005389	reproductive system phenotype	Fetub<tm1Wja>/Fetub<tm1Wja>	B6.Cg-Fetub<tm1Wja>	Y	23562279
MGI:5514277	F	MP:0000242	impaired fertilization	Fetub<tm1Wja>/Fetub<tm1Wja>	B6.Cg-Fetub<tm1Wja>	N	23562279
MGI:5514277	F	MP:0003696	abnormal zona pellucida morphology	Fetub<tm1Wja>/Fetub<tm1Wja>	B6.Cg-Fetub<tm1Wja>	N	23562279
MGI:5514277	F	MP:0001926	female infertility	Fetub<tm1Wja>/Fetub<tm1Wja>	B6.Cg-Fetub<tm1Wja>	N	23562279
MGI:5514278	F	MP:0000242	impaired fertilization	Fetub<tm1Wja>/Fetub<tm1Wja>	D2.Cg-Fetub<tm1Wja>	N	23562279
MGI:5514278	F	MP:0003696	abnormal zona pellucida morphology	Fetub<tm1Wja>/Fetub<tm1Wja>	D2.Cg-Fetub<tm1Wja>	N	23562279
MGI:5514278	M	MP:0005389	reproductive system phenotype	Fetub<tm1Wja>/Fetub<tm1Wja>	D2.Cg-Fetub<tm1Wja>	Y	23562279
MGI:5514278	F	MP:0001926	female infertility	Fetub<tm1Wja>/Fetub<tm1Wja>	D2.Cg-Fetub<tm1Wja>	N	23562279
MGI:5515317	M	MP:0002460	decreased immunoglobulin level	Sh2d1a<tm1Lyin>/Y	involves: 129S2/SvPas * C57BL/6	N	12966553
MGI:5515317	M	MP:0001790	abnormal immune system physiology	Sh2d1a<tm1Lyin>/Y	involves: 129S2/SvPas * C57BL/6	N	12966553
MGI:5515317	M	MP:0001805	decreased IgG level	Sh2d1a<tm1Lyin>/Y	involves: 129S2/SvPas * C57BL/6	N	12966553
MGI:5515317	M	MP:0008078	increased CD8-positive, alpha-beta T cell number	Sh2d1a<tm1Lyin>/Y	involves: 129S2/SvPas * C57BL/6	N	12966553
MGI:5515317	M	MP:0002492	decreased IgE level	Sh2d1a<tm1Lyin>/Y	involves: 129S2/SvPas * C57BL/6	N	12966553
MGI:5515317	M	MP:0002499	chronic inflammation	Sh2d1a<tm1Lyin>/Y	involves: 129S2/SvPas * C57BL/6	N	12966553
MGI:5515353	F	MP:0009082	uterus cyst	Chd2<Gt(RRBO46)Byg>/Chd2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	18386809
MGI:5515353	F	MP:0009092	endometrium hyperplasia	Chd2<Gt(RRBO46)Byg>/Chd2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	18386809
MGI:5515634	F	MP:0004762	increased anti-double stranded DNA antibody level	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0005327	abnormal mesangial cell morphology	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0002135	abnormal kidney morphology	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0004794	increased anti-nuclear antigen antibody level	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0002962	increased urine protein level	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0001859	kidney inflammation	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0003725	increased autoantibody level	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0002461	increased immunoglobulin level	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0009338	increased splenocyte number	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0008192	abnormal germinal center B cell physiology	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0001790	abnormal immune system physiology	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0002493	increased IgG level	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0008705	increased interleukin-6 secretion	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0008177	increased germinal center B cell number	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0010188	abnormal T follicular helper cell differentiation	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0010186	increased T follicular helper cell number	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515634	F	MP:0008481	increased spleen germinal center number	Prdm1<tm1Clme>/Prdm1<tm1Clme>,Tg(Itgax-cre)1-1Reiz/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	21948081
MGI:5515728	M	MP:0006036	abnormal mitochondrial physiology	Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	23217260
MGI:5515728	M	MP:0002079	increased circulating insulin level	Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	23217260
MGI:5515728	M	MP:0001777	abnormal body temperature homeostasis	Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	23217260
MGI:5515728	M	MP:0011168	abnormal fat cell differentiation	Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	23217260
MGI:5515728	M	MP:0002971	abnormal brown adipose tissue morphology	Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	23217260
MGI:5515728	M	MP:0011049	impaired adaptive thermogenesis	Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	23217260
MGI:5515728	M	MP:0001261	obese	Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	23217260
MGI:5515728	M	MP:0004890	decreased energy expenditure	Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	23217260
MGI:5515728	M	MP:0003982	increased cholesterol level	Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	23217260
MGI:5515728	M	MP:0011636	disorganized mitochondrial cristae	Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	23217260
MGI:5515728	M	MP:0001260	increased body weight	Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	23217260
MGI:5515728	M	MP:0005293	impaired glucose tolerance	Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	23217260
MGI:5515728	M	MP:0001554	increased circulating free fatty acids level	Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	N	23217260
MGI:5515733	M	MP:0005375	adipose tissue phenotype	Gt(ROSA)26Sor<tm1(Stat3*A661C*N663C)Sbkv>/?,Tg(Fabp4-cre/ERT2)1Ipc/0,Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	involves: 129P2/OlaHsd * C57BL/6 * SJL	Y	23217260
MGI:5515733	M	MP:0005376	homeostasis/metabolism phenotype	Gt(ROSA)26Sor<tm1(Stat3*A661C*N663C)Sbkv>/?,Tg(Fabp4-cre/ERT2)1Ipc/0,Tyk2<tm1Shmd>/Tyk2<tm1Shmd>	involves: 129P2/OlaHsd * C57BL/6 * SJL	Y	23217260
MGI:5515770	F	MP:0005376	homeostasis/metabolism phenotype	Car5b<tm1Sly>/Car5b<tm1Sly>	involves: 129S1/Sv * C57BL/6	Y	23589845
MGI:5515770	F	MP:0010768	mortality/aging	Car5b<tm1Sly>/Car5b<tm1Sly>	involves: 129S1/Sv * C57BL/6	Y	23589845
MGI:5515772	M	MP:0005376	homeostasis/metabolism phenotype	Car5b<tm1Sly>/Y	involves: 129S1/Sv * C57BL/6	Y	23589845
MGI:5515772	M	MP:0010768	mortality/aging	Car5b<tm1Sly>/Y	involves: 129S1/Sv * C57BL/6	Y	23589845
MGI:5515773	F	MP:0011110	preweaning lethality, incomplete penetrance	Car5a<tm1Sly>/Car5a<tm1Sly>,Car5b<tm1Sly>/Car5b<tm1Sly>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23589845
MGI:5515773	F	MP:0001265	decreased body size	Car5a<tm1Sly>/Car5a<tm1Sly>,Car5b<tm1Sly>/Car5b<tm1Sly>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23589845
MGI:5515773	F	MP:0005309	increased circulating ammonia level	Car5a<tm1Sly>/Car5a<tm1Sly>,Car5b<tm1Sly>/Car5b<tm1Sly>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23589845
MGI:5515773	F	MP:0003674	oxidative stress	Car5a<tm1Sly>/Car5a<tm1Sly>,Car5b<tm1Sly>/Car5b<tm1Sly>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22109883
MGI:5515773	F	MP:0005560	decreased circulating glucose level	Car5a<tm1Sly>/Car5a<tm1Sly>,Car5b<tm1Sly>/Car5b<tm1Sly>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23589845
MGI:5515773	F	MP:0002083	premature death	Car5a<tm1Sly>/Car5a<tm1Sly>,Car5b<tm1Sly>/Car5b<tm1Sly>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23589845
MGI:5515774	M	MP:0003674	oxidative stress	Car5a<tm1Sly>/Car5a<tm1Sly>,Car5b<tm1Sly>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	22109883
MGI:5515774	M	MP:0002083	premature death	Car5a<tm1Sly>/Car5a<tm1Sly>,Car5b<tm1Sly>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23589845
MGI:5515774	M	MP:0005560	decreased circulating glucose level	Car5a<tm1Sly>/Car5a<tm1Sly>,Car5b<tm1Sly>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23589845
MGI:5515774	M	MP:0001265	decreased body size	Car5a<tm1Sly>/Car5a<tm1Sly>,Car5b<tm1Sly>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23589845
MGI:5515774	M	MP:0005309	increased circulating ammonia level	Car5a<tm1Sly>/Car5a<tm1Sly>,Car5b<tm1Sly>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23589845
MGI:5515774	M	MP:0011110	preweaning lethality, incomplete penetrance	Car5a<tm1Sly>/Car5a<tm1Sly>,Car5b<tm1Sly>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23589845
MGI:5515775	M	MP:0002875	decreased erythrocyte cell number	Myo1c<tm1.1Biat>/Myo1c<tm1.1Biat>	B6N.129S2-Myo1c<tm1.1Biat>	N	23593477
MGI:5515775	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Myo1c<tm1.1Biat>/Myo1c<tm1.1Biat>	B6N.129S2-Myo1c<tm1.1Biat>	N	23593477
MGI:5515775	M	MP:0005561	increased mean corpuscular hemoglobin	Myo1c<tm1.1Biat>/Myo1c<tm1.1Biat>	B6N.129S2-Myo1c<tm1.1Biat>	N	23593477
MGI:5515892	M	MP:0001922	reduced male fertility	Pmp22<Tr-2J>/Pmp22<+>	C57BL/6J-Pmp22<Tr-2J>/GrsrJ	N	MGI:5515889
MGI:5516018	M	MP:0001925	male infertility	Akap9<tm1b(KOMP)Wtsi>/Akap9<tm1b(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N * FVB/N	N	23608191
MGI:5516019	M	MP:0005159	azoospermia	Akap9<mei2-5>/Akap9<mei2-5>	involves: 129S1/Sv	N	23608191
MGI:5516019	M	MP:0004109	abnormal Sertoli cell development	Akap9<mei2-5>/Akap9<mei2-5>	involves: 129S1/Sv	N	23608191
MGI:5516019	M	MP:0006379	abnormal spermatocyte morphology	Akap9<mei2-5>/Akap9<mei2-5>	involves: 129S1/Sv	N	23608191
MGI:5516019	M	MP:0001156	abnormal spermatogenesis	Akap9<mei2-5>/Akap9<mei2-5>	involves: 129S1/Sv	N	23608191
MGI:5516020	M	MP:0001155	arrest of spermatogenesis	Akap9<repro12>/Akap9<repro12>	involves: C57BL/6J	N	23608191
MGI:5516021	M	MP:0005159	azoospermia	Akap9<mei2-5>/Akap9<repro12>	involves: 129S1/Sv * C57BL/6J	N	23608191
MGI:5516021	M	MP:0001155	arrest of spermatogenesis	Akap9<mei2-5>/Akap9<repro12>	involves: 129S1/Sv * C57BL/6J	N	23608191
MGI:5516021	M	MP:0001156	abnormal spermatogenesis	Akap9<mei2-5>/Akap9<repro12>	involves: 129S1/Sv * C57BL/6J	N	23608191
MGI:5516022	M	MP:0001156	abnormal spermatogenesis	Akap9<repro12>/Akap9<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N * FVB/N	N	23608191
MGI:5516022	M	MP:0005159	azoospermia	Akap9<repro12>/Akap9<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N * FVB/N	N	23608191
MGI:5516059	M	MP:0011090	perinatal lethality, incomplete penetrance	Kdm6a<Gt(RRA094)Byg>/Y	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516059	M	MP:0000914	exencephaly	Kdm6a<Gt(RRA094)Byg>/Y	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516059	M	MP:0002083	premature death	Kdm6a<Gt(RRA094)Byg>/Y	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516059	M	MP:0009703	decreased birth body size	Kdm6a<Gt(RRA094)Byg>/Y	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516059	M	MP:0001265	decreased body size	Kdm6a<Gt(RRA094)Byg>/Y	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516060	F	MP:0002925	abnormal cardiovascular development	Kdm6a<Gt(RRA094)Byg>/Kdm6a<Gt(RRA094)Byg>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516060	F	MP:0001787	pericardial edema	Kdm6a<Gt(RRA094)Byg>/Kdm6a<Gt(RRA094)Byg>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516060	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Kdm6a<Gt(RRA094)Byg>/Kdm6a<Gt(RRA094)Byg>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516060	F	MP:0000266	abnormal heart morphology	Kdm6a<Gt(RRA094)Byg>/Kdm6a<Gt(RRA094)Byg>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516060	F	MP:0001698	decreased embryo size	Kdm6a<Gt(RRA094)Byg>/Kdm6a<Gt(RRA094)Byg>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516060	F	MP:0000929	open neural tube	Kdm6a<Gt(RRA094)Byg>/Kdm6a<Gt(RRA094)Byg>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516060	F	MP:0004251	failure of heart looping	Kdm6a<Gt(RRA094)Byg>/Kdm6a<Gt(RRA094)Byg>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516060	F	MP:0000280	thin ventricular wall	Kdm6a<Gt(RRA094)Byg>/Kdm6a<Gt(RRA094)Byg>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516060	F	MP:0001722	pale yolk sac	Kdm6a<Gt(RRA094)Byg>/Kdm6a<Gt(RRA094)Byg>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516060	F	MP:0002188	small heart	Kdm6a<Gt(RRA094)Byg>/Kdm6a<Gt(RRA094)Byg>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516060	F	MP:0010503	myocardial trabeculae hypoplasia	Kdm6a<Gt(RRA094)Byg>/Kdm6a<Gt(RRA094)Byg>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516060	F	MP:0010725	thin interventricular septum	Kdm6a<Gt(RRA094)Byg>/Kdm6a<Gt(RRA094)Byg>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516061	M	MP:0000280	thin ventricular wall	Kdm6a<Gt(RRA094)Byg>/Y,X/Uty<Gt(XS0378)Wtsi>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516061	M	MP:0001787	pericardial edema	Kdm6a<Gt(RRA094)Byg>/Y,X/Uty<Gt(XS0378)Wtsi>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516061	M	MP:0000266	abnormal heart morphology	Kdm6a<Gt(RRA094)Byg>/Y,X/Uty<Gt(XS0378)Wtsi>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516061	M	MP:0010503	myocardial trabeculae hypoplasia	Kdm6a<Gt(RRA094)Byg>/Y,X/Uty<Gt(XS0378)Wtsi>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516061	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Kdm6a<Gt(RRA094)Byg>/Y,X/Uty<Gt(XS0378)Wtsi>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516061	M	MP:0010725	thin interventricular septum	Kdm6a<Gt(RRA094)Byg>/Y,X/Uty<Gt(XS0378)Wtsi>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516061	M	MP:0004251	failure of heart looping	Kdm6a<Gt(RRA094)Byg>/Y,X/Uty<Gt(XS0378)Wtsi>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516061	M	MP:0002188	small heart	Kdm6a<Gt(RRA094)Byg>/Y,X/Uty<Gt(XS0378)Wtsi>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516062	M	MP:0001265	decreased body size	Kdm6a<tm1b(EUCOMM)Wtsi>/Y	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516062	M	MP:0000914	exencephaly	Kdm6a<tm1b(EUCOMM)Wtsi>/Y	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516062	M	MP:0011090	perinatal lethality, incomplete penetrance	Kdm6a<tm1b(EUCOMM)Wtsi>/Y	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516062	M	MP:0002083	premature death	Kdm6a<tm1b(EUCOMM)Wtsi>/Y	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516062	M	MP:0009703	decreased birth body size	Kdm6a<tm1b(EUCOMM)Wtsi>/Y	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516063	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Kdm6a<tm1b(EUCOMM)Wtsi>/Kdm6a<tm1b(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516063	F	MP:0010725	thin interventricular septum	Kdm6a<tm1b(EUCOMM)Wtsi>/Kdm6a<tm1b(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516063	F	MP:0001722	pale yolk sac	Kdm6a<tm1b(EUCOMM)Wtsi>/Kdm6a<tm1b(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516063	F	MP:0000280	thin ventricular wall	Kdm6a<tm1b(EUCOMM)Wtsi>/Kdm6a<tm1b(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516063	F	MP:0001698	decreased embryo size	Kdm6a<tm1b(EUCOMM)Wtsi>/Kdm6a<tm1b(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516063	F	MP:0002188	small heart	Kdm6a<tm1b(EUCOMM)Wtsi>/Kdm6a<tm1b(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516063	F	MP:0004251	failure of heart looping	Kdm6a<tm1b(EUCOMM)Wtsi>/Kdm6a<tm1b(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516063	F	MP:0001787	pericardial edema	Kdm6a<tm1b(EUCOMM)Wtsi>/Kdm6a<tm1b(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516063	F	MP:0002925	abnormal cardiovascular development	Kdm6a<tm1b(EUCOMM)Wtsi>/Kdm6a<tm1b(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516063	F	MP:0010503	myocardial trabeculae hypoplasia	Kdm6a<tm1b(EUCOMM)Wtsi>/Kdm6a<tm1b(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516063	F	MP:0000929	open neural tube	Kdm6a<tm1b(EUCOMM)Wtsi>/Kdm6a<tm1b(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516063	F	MP:0000266	abnormal heart morphology	Kdm6a<tm1b(EUCOMM)Wtsi>/Kdm6a<tm1b(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516064	M	MP:0011090	perinatal lethality, incomplete penetrance	Kdm6a<tm1c(EUCOMM)Wtsi>/Y	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516065	F	MP:0000929	open neural tube	Kdm6a<tm1c(EUCOMM)Wtsi>/Kdm6a<tm1c(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516065	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Kdm6a<tm1c(EUCOMM)Wtsi>/Kdm6a<tm1c(EUCOMM)Wtsi>	either: (involves: C57BL/6 * CD-1) or (involves: 129 * C57BL/6 * CD-1)	N	23028370
MGI:5516066	F	MP:0011099	lethality throughout fetal growth and development, complete penetrance	Kdm6a<tm1c(EUCOMM)Wtsi>/Kdm6a<tm1c(EUCOMM)Wtsi>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	either: (involves: C57BL/6 * CBA * CD-1) or (involves: 129 * C57BL/6 * CBA * CD-1)	N	23028370
MGI:5516067	M	MP:0010768	mortality/aging	Kdm6a<tm1c(EUCOMM)Wtsi>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	either: (involves: C57BL/6 * CBA * CD-1) or (involves: 129 * C57BL/6 * CBA * CD-1)	Y	23028370
MGI:5516068	M	MP:0002169	no abnormal phenotype detected	X/Uty<Gt(XS0378)Wtsi>	either: (involves: 129 * CD-1) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129P2/OlaHsd * C57BL/6 * CD-1)	N	23028370
MGI:5516118	M	MP:0009763	increased susceptibility to induced morbidity/mortality	Mmp2<tm1Ito>/Mmp2<tm1Ito>,Timp3<tm1Osya>/Timp3<tm1Osya>	involves: 129P2/OlaHsd * C57BL/6	N	23144462
MGI:5516118	M	MP:0009870	abnormal abdominal aorta morphology	Mmp2<tm1Ito>/Mmp2<tm1Ito>,Timp3<tm1Osya>/Timp3<tm1Osya>	involves: 129P2/OlaHsd * C57BL/6	N	23144462
MGI:5516118	M	MP:0009866	abnormal aorta wall morphology	Mmp2<tm1Ito>/Mmp2<tm1Ito>,Timp3<tm1Osya>/Timp3<tm1Osya>	involves: 129P2/OlaHsd * C57BL/6	N	23144462
MGI:5516118	M	MP:0031274	increased susceptibility to induced aneurysm formation	Mmp2<tm1Ito>/Mmp2<tm1Ito>,Timp3<tm1Osya>/Timp3<tm1Osya>	involves: 129P2/OlaHsd * C57BL/6	N	23144462
MGI:5516118	M	MP:0010139	aortitis	Mmp2<tm1Ito>/Mmp2<tm1Ito>,Timp3<tm1Osya>/Timp3<tm1Osya>	involves: 129P2/OlaHsd * C57BL/6	N	23144462
MGI:5516191	M	MP:0003964	abnormal noradrenaline level	Slc6a2<tm1.1Mkh>/Slc6a2<+>	B6.129S6-Slc6a2<tm1.1Mkh>	N	23580201
MGI:5516194	M	MP:0002079	increased circulating insulin level	Lcmt1<Gt(CSC099)Byg>/Lcmt1<Gt(CSC099)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23840384
MGI:5516430	F	MP:0006309	decreased retina ganglion cell number	Gucy1a1<tm1.1Brou>/Gucy1a1<tm1.1Brou>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	N	23527308
MGI:5516430	F	MP:0005206	abnormal aqueous humor	Gucy1a1<tm1.1Brou>/Gucy1a1<tm1.1Brou>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	N	23527308
MGI:5516430	F	MP:0005253	abnormal eye physiology	Gucy1a1<tm1.1Brou>/Gucy1a1<tm1.1Brou>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	N	23527308
MGI:5516430	F	MP:0006303	abnormal retina nerve fiber layer morphology	Gucy1a1<tm1.1Brou>/Gucy1a1<tm1.1Brou>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	N	23527308
MGI:5516430	F	MP:0005258	ocular hypertension	Gucy1a1<tm1.1Brou>/Gucy1a1<tm1.1Brou>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	N	23527308
MGI:5516430	F	MP:0001330	abnormal optic nerve morphology	Gucy1a1<tm1.1Brou>/Gucy1a1<tm1.1Brou>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	N	23527308
MGI:5517355	F	MP:0004762	increased anti-double stranded DNA antibody level	Ptpn22<tm1.1Draw>/Ptpn22<+>	involves: 129 * C57BL/6	N	23619366
MGI:5517369	F	MP:0000627	abnormal mammary gland morphology	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	C.129-Cdkn2c<tm1Yxi>	N	22777348
MGI:5517369	F	MP:0010299	increased mammary gland tumor incidence	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	C.129-Cdkn2c<tm1Yxi>	N	22777348
MGI:5517370	F	MP:0010299	increased mammary gland tumor incidence	Brca1<tm1Bhk>/Brca1<+>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	C.129-Cdkn2c<tm1Yxi> Brca1<tm1Bhk>	N	22777348
MGI:5517370	F	MP:0001883	increased mammary adenocarcinoma incidence	Brca1<tm1Bhk>/Brca1<+>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	C.129-Cdkn2c<tm1Yxi> Brca1<tm1Bhk>	N	22777348
MGI:5517370	F	MP:0000627	abnormal mammary gland morphology	Brca1<tm1Bhk>/Brca1<+>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	C.129-Cdkn2c<tm1Yxi> Brca1<tm1Bhk>	N	22777348
MGI:5517482	M	MP:0001353	increased aggression towards mice	Syn1<tm1Pggd>/Syn1<tm1Pggd>	B6.129P2-Syn1<tm1Pggd>	N	23280234
MGI:5517482	M	MP:0002969	impaired social transmission of food preference	Syn1<tm1Pggd>/Syn1<tm1Pggd>	B6.129P2-Syn1<tm1Pggd>	N	23280234
MGI:5517482	M	MP:0001360	abnormal social investigation	Syn1<tm1Pggd>/Syn1<tm1Pggd>	B6.129P2-Syn1<tm1Pggd>	N	23280234
MGI:5517482	M	MP:0002572	abnormal emotion/affect behavior	Syn1<tm1Pggd>/Syn1<tm1Pggd>	B6.129P2-Syn1<tm1Pggd>	N	23280234
MGI:5517482	M	MP:0005394	taste/olfaction phenotype	Syn1<tm1Pggd>/Syn1<tm1Pggd>	B6.129P2-Syn1<tm1Pggd>	Y	23280234
MGI:5517484	M	MP:0001353	increased aggression towards mice	Syn2<tm1Pggd>/Syn2<tm1Pggd>	B6.1129-Syn2<tm1Pggd>	N	23280234
MGI:5517484	M	MP:0001441	increased grooming behavior	Syn2<tm1Pggd>/Syn2<tm1Pggd>	B6.1129-Syn2<tm1Pggd>	N	23280234
MGI:5517484	M	MP:0002572	abnormal emotion/affect behavior	Syn2<tm1Pggd>/Syn2<tm1Pggd>	B6.1129-Syn2<tm1Pggd>	N	23280234
MGI:5517484	M	MP:0005394	taste/olfaction phenotype	Syn2<tm1Pggd>/Syn2<tm1Pggd>	B6.1129-Syn2<tm1Pggd>	Y	23280234
MGI:5517484	M	MP:0021111	decreased social investigation	Syn2<tm1Pggd>/Syn2<tm1Pggd>	B6.1129-Syn2<tm1Pggd>	N	23280234
MGI:5517484	M	MP:0001360	abnormal social investigation	Syn2<tm1Pggd>/Syn2<tm1Pggd>	B6.1129-Syn2<tm1Pggd>	N	23280234
MGI:5517485	M	MP:0001360	abnormal social investigation	Syn3<tm1Pggd>/Syn3<tm1Pggd>	B6.129X1-Syn3<tm1Jfe>	N	23280234
MGI:5517485	M	MP:0005394	taste/olfaction phenotype	Syn3<tm1Pggd>/Syn3<tm1Pggd>	B6.129X1-Syn3<tm1Jfe>	Y	23280234
MGI:5517485	M	MP:0003863	decreased aggression towards mice	Syn3<tm1Pggd>/Syn3<tm1Pggd>	B6.129X1-Syn3<tm1Jfe>	N	23280234
MGI:5517485	M	MP:0002969	impaired social transmission of food preference	Syn3<tm1Pggd>/Syn3<tm1Pggd>	B6.129X1-Syn3<tm1Jfe>	N	23280234
MGI:5517593	M	MP:0005164	abnormal response to injury	Gnrhr<tm1(GNRHR1)Xen>/Gnrhr<tm1(GNRHR1)Xen>	involves: C57BL/6 * C57BL/6JOlaHsd	N	23632635
MGI:5517593	F	MP:0001927	abnormal estrous cycle	Gnrhr<tm1(GNRHR1)Xen>/Gnrhr<tm1(GNRHR1)Xen>	involves: C57BL/6 * C57BL/6JOlaHsd	N	23632635
MGI:5517593	F	MP:0005182	increased circulating estradiol level	Gnrhr<tm1(GNRHR1)Xen>/Gnrhr<tm1(GNRHR1)Xen>	involves: C57BL/6 * C57BL/6JOlaHsd	N	23632635
MGI:5517593	M	MP:0002780	decreased circulating testosterone level	Gnrhr<tm1(GNRHR1)Xen>/Gnrhr<tm1(GNRHR1)Xen>	involves: C57BL/6 * C57BL/6JOlaHsd	N	23632635
MGI:5517593	F	MP:0009006	prolonged estrous cycle	Gnrhr<tm1(GNRHR1)Xen>/Gnrhr<tm1(GNRHR1)Xen>	involves: C57BL/6 * C57BL/6JOlaHsd	N	23632635
MGI:5517593	M	MP:0003969	abnormal luteinizing hormone level	Gnrhr<tm1(GNRHR1)Xen>/Gnrhr<tm1(GNRHR1)Xen>	involves: C57BL/6 * C57BL/6JOlaHsd	N	23632635
MGI:5517593	F	MP:0009020	prolonged metestrus	Gnrhr<tm1(GNRHR1)Xen>/Gnrhr<tm1(GNRHR1)Xen>	involves: C57BL/6 * C57BL/6JOlaHsd	N	23632635
MGI:5517593	F	MP:0001923	reduced female fertility	Gnrhr<tm1(GNRHR1)Xen>/Gnrhr<tm1(GNRHR1)Xen>	involves: C57BL/6 * C57BL/6JOlaHsd	N	23632635
MGI:5517700	M	MP:0003862	decreased aggression towards male mice	Kirrel3<tm1.1Jfcl>/Kirrel3<tm1.1Jfcl>	Not Specified	N	23637329
MGI:5517700	M	MP:0002566	abnormal sexual interaction	Kirrel3<tm1.1Jfcl>/Kirrel3<tm1.1Jfcl>	Not Specified	N	23637329
MGI:5518434	M	MP:0001922	reduced male fertility	Pygo1<tm1.1Kba>/Pygo1<tm1.1Kba>,Pygo2<tm1.1Kba>/Pygo2<tm1.1Kba>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NTac	N	23637336
MGI:5518434	M	MP:0002687	oligozoospermia	Pygo1<tm1.1Kba>/Pygo1<tm1.1Kba>,Pygo2<tm1.1Kba>/Pygo2<tm1.1Kba>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NTac	N	23637336
MGI:5518434	M	MP:0006380	abnormal spermatid morphology	Pygo1<tm1.1Kba>/Pygo1<tm1.1Kba>,Pygo2<tm1.1Kba>/Pygo2<tm1.1Kba>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NTac	N	23637336
MGI:5518434	M	MP:0001925	male infertility	Pygo1<tm1.1Kba>/Pygo1<tm1.1Kba>,Pygo2<tm1.1Kba>/Pygo2<tm1.1Kba>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NTac	N	23637336
MGI:5518660	M	MP:0002169	no abnormal phenotype detected	Itm2a<tm1Buck>/Y	involves: C57BL/6	N	23650549
MGI:5518662	F	MP:0002169	no abnormal phenotype detected	Itm2a<tm1Buck>/Itm2a<tm1Buck>	involves: C57BL/6	N	23650549
MGI:5518663	M	MP:0002169	no abnormal phenotype detected	Itm2a<tm1.1Buck>/Y	involves: C57BL/6	N	23650549
MGI:5518664	F	MP:0002169	no abnormal phenotype detected	Itm2a<tm1.1Buck>/Itm2a<tm1.1Buck>	involves: C57BL/6	N	23650549
MGI:5518665	M	MP:0002169	no abnormal phenotype detected	Itm2a<tm1.2Buck>/Y	involves: BALB/c * C57BL/6	N	23650549
MGI:5518666	F	MP:0002169	no abnormal phenotype detected	Itm2a<tm1.2Buck>/Itm2a<tm1.2Buck>	involves: BALB/c * C57BL/6	N	23650549
MGI:5518667	M	MP:0002169	no abnormal phenotype detected	Itm2a<tm1.1Buck>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: C57BL/6	N	23650549
MGI:5518668	M	MP:0002151	abnormal neural tube morphology	Itm2a<tm1.1Buck>/Y,Pax3<tm1(cre)Joe>/Pax3<tm1(cre)Joe>	involves: C57BL/6	N	23650549
MGI:5518669	M	MP:0002151	abnormal neural tube morphology	Itm2a<tm1.2Buck>/Y,Pax3<tm4Buck>/Pax3<tm4Buck>	involves: C57BL/6	N	23650549
MGI:5518852	F	MP:0009406	decreased skeletal muscle fiber number	Mbnl3<tm1.1Sws>/Mbnl3<tm1.1Sws>	involves: BALB/c * C57BL/6 * C57BL/6J	N	23660517
MGI:5518852	F	MP:0010053	decreased grip strength	Mbnl3<tm1.1Sws>/Mbnl3<tm1.1Sws>	involves: BALB/c * C57BL/6 * C57BL/6J	N	23660517
MGI:5518852	F	MP:0013239	impaired skeletal muscle regeneration	Mbnl3<tm1.1Sws>/Mbnl3<tm1.1Sws>	involves: BALB/c * C57BL/6 * C57BL/6J	N	23660517
MGI:5518852	F	MP:0009400	decreased skeletal muscle fiber size	Mbnl3<tm1.1Sws>/Mbnl3<tm1.1Sws>	involves: BALB/c * C57BL/6 * C57BL/6J	N	23660517
MGI:5518853	M	MP:0009406	decreased skeletal muscle fiber number	Mbnl3<tm1.1Sws>/Y	involves: BALB/c * C57BL/6 * C57BL/6J	N	23660517
MGI:5518853	M	MP:0010053	decreased grip strength	Mbnl3<tm1.1Sws>/Y	involves: BALB/c * C57BL/6 * C57BL/6J	N	23660517
MGI:5518853	M	MP:0013239	impaired skeletal muscle regeneration	Mbnl3<tm1.1Sws>/Y	involves: BALB/c * C57BL/6 * C57BL/6J	N	23660517
MGI:5518853	M	MP:0009400	decreased skeletal muscle fiber size	Mbnl3<tm1.1Sws>/Y	involves: BALB/c * C57BL/6 * C57BL/6J	N	23660517
MGI:5519068	M	MP:0001265	decreased body size	Lin28b<tm1.1Gqda>/Lin28b<tm1.1Gqda>	involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	N	23666760
MGI:5519072	M	MP:0001258	decreased body length	Lin28a<tm1Gqda>/Lin28a<tm1.1Gqda>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * 129S4/SvJae * C57BL/6 * FVB/N	N	23666760
MGI:5519072	M	MP:0001265	decreased body size	Lin28a<tm1Gqda>/Lin28a<tm1.1Gqda>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * 129S4/SvJae * C57BL/6 * FVB/N	N	23666760
MGI:5519073	M	MP:0001265	decreased body size	Lin28b<tm1Gqda>/Lin28b<tm1.1Gqda>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	N	23666760
MGI:5519076	M	MP:0001265	decreased body size	Lin28b<tm1Gqda>/Lin28b<tm1Gqda>,Myf5<tm1(cre)Mrc>/Myf5<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	23666760
MGI:5519211	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0001932	abnormal spermiogenesis	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0008261	arrest of male meiosis	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0002675	asthenozoospermia	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0005159	azoospermia	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0014052	increased male germ cell apoptosis	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0001935	decreased litter size	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0001925	male infertility	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0001146	abnormal testis morphology	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0004852	decreased testis weight	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0002687	oligozoospermia	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0001156	abnormal spermatogenesis	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0001147	small testis	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0005578	teratozoospermia	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	M	MP:0001922	reduced male fertility	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	N	23674551
MGI:5519211	F	MP:0005389	reproductive system phenotype	Tex19.1<tm1.2Ics>/Tex19.1<tm1.2Ics>	involves: C57BL/6	Y	23674551
MGI:5519974	M	MP:0000477	abnormal intestine morphology	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0009293	decreased inguinal fat pad weight	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0009295	decreased interscapular fat pad weight	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0009299	decreased mesenteric fat pad weight	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0002644	decreased circulating triglyceride level	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0002628	hepatic steatosis	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0005290	decreased oxygen consumption	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0002631	abnormal epididymis morphology	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0005559	increased circulating glucose level	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0002702	decreased circulating free fatty acids level	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0001556	increased circulating HDL cholesterol level	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0008964	decreased carbon dioxide production	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0009355	increased liver triglyceride level	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0004890	decreased energy expenditure	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0001559	hyperglycemia	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0011939	increased food intake	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0011110	preweaning lethality, incomplete penetrance	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0002981	increased liver weight	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0000005	increased brown adipose tissue amount	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0011174	lipodystrophy	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0005376	homeostasis/metabolism phenotype	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	Y	23680914
MGI:5519974	M	MP:0002118	abnormal lipid homeostasis	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0005386	behavior/neurological phenotype	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	Y	23680914
MGI:5519974	M	MP:0030968	decreased circulating adiponectin level	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0009283	decreased gonadal fat pad weight	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0005293	impaired glucose tolerance	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0005331	insulin resistance	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0000599	enlarged liver	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0001925	male infertility	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0005668	decreased circulating leptin level	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0002079	increased circulating insulin level	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5519974	M	MP:0001262	decreased body weight	Bscl2<tm1Geno>/Bscl2<tm1Geno>	B6.129P2-Bscl2<tm1Geno>	N	23680914
MGI:5520094	M	MP:0002687	oligozoospermia	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520094	M	MP:0009838	abnormal sperm axoneme morphology	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520094	M	MP:0002675	asthenozoospermia	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520094	M	MP:0004852	decreased testis weight	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520094	M	MP:0009837	abnormal sperm end piece morphology	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520094	M	MP:0009835	absent sperm annulus	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520094	M	MP:0009836	abnormal sperm principal piece morphology	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520094	F	MP:0005389	reproductive system phenotype	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	Y	23446454
MGI:5520094	M	MP:0009834	abnormal sperm annulus morphology	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520094	M	MP:0009831	abnormal sperm midpiece morphology	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520094	M	MP:0009237	kinked sperm flagellum	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520094	M	MP:0004929	decreased epididymis weight	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520094	M	MP:0001925	male infertility	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520094	M	MP:0030590	abnormal sperm fibrous sheath morphology	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520094	M	MP:0008892	abnormal sperm flagellum morphology	Eno4<Gt(RRF299)Byg>/Eno4<Gt(RRF299)Byg>	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6)	N	23446454
MGI:5520959	M	MP:0000242	impaired fertilization	Prss37<tm1Zgwg>/Prss37<tm1Zgwg>	involves: 129S6/SvEvTac * C57BL/6J	N	23553430
MGI:5520959	M	MP:0001925	male infertility	Prss37<tm1Zgwg>/Prss37<tm1Zgwg>	involves: 129S6/SvEvTac * C57BL/6J	N	23553430
MGI:5520959	M	MP:0030978	impaired binding of sperm to zona pellucida	Prss37<tm1Zgwg>/Prss37<tm1Zgwg>	involves: 129S6/SvEvTac * C57BL/6J	N	23553430
MGI:5520959	M	MP:0031012	impaired sperm migration in female genital tract	Prss37<tm1Zgwg>/Prss37<tm1Zgwg>	involves: 129S6/SvEvTac * C57BL/6J	N	23553430
MGI:5521183	M	MP:0005378	growth/size/body region phenotype	Slc6a4<tm2.1Rbl>/Slc6a4<tm2.1Rbl>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J	Y	19960097
MGI:5521202	M	MP:0009456	impaired cued conditioning behavior	Tg(Thy1-Tcf4)1Mjro/0	involves: C57BL/6N * FVB/N	N	20434134
MGI:5521202	M	MP:0009454	impaired contextual conditioning behavior	Tg(Thy1-Tcf4)1Mjro/0	involves: C57BL/6N * FVB/N	N	23069005
MGI:5521202	M	MP:0009454	impaired contextual conditioning behavior	Tg(Thy1-Tcf4)1Mjro/0	involves: C57BL/6N * FVB/N	N	20434134
MGI:5521202	M	MP:0002635	reduced sensorimotor gating	Tg(Thy1-Tcf4)1Mjro/0	involves: C57BL/6N * FVB/N	N	20434134
MGI:5521202	M	MP:0012307	impaired spatial learning	Tg(Thy1-Tcf4)1Mjro/0	involves: C57BL/6N * FVB/N	N	20434134
MGI:5521202	M	MP:0003088	abnormal prepulse inhibition	Tg(Thy1-Tcf4)1Mjro/0	involves: C57BL/6N * FVB/N	N	20434134
MGI:5521202	M	MP:0009456	impaired cued conditioning behavior	Tg(Thy1-Tcf4)1Mjro/0	involves: C57BL/6N * FVB/N	N	23069005
MGI:5521202	M	MP:0002062	abnormal associative learning	Tg(Thy1-Tcf4)1Mjro/0	involves: C57BL/6N * FVB/N	N	23069005
MGI:5521202	M	MP:0002797	increased thigmotaxis	Tg(Thy1-Tcf4)1Mjro/0	involves: C57BL/6N * FVB/N	N	20434134
MGI:5521206	M	MP:0009456	impaired cued conditioning behavior	Tg(Thy1-Tcf4)1Mjro/0	B6N.FVB-Tg(Thy1-Tcf4)1Mjro	N	20434134
MGI:5521206	M	MP:0009454	impaired contextual conditioning behavior	Tg(Thy1-Tcf4)1Mjro/0	B6N.FVB-Tg(Thy1-Tcf4)1Mjro	N	20434134
MGI:5521285	F	MP:0000222	decreased neutrophil cell number	Mthfd1<tm1.1Rzn>/Mthfd1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	23704330
MGI:5521285	F	MP:0003718	maternal effect	Mthfd1<tm1.1Rzn>/Mthfd1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	23704330
MGI:5521285	F	MP:0001260	increased body weight	Mthfd1<tm1.1Rzn>/Mthfd1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	23704330
MGI:5521285	F	MP:0000221	decreased leukocyte cell number	Mthfd1<tm1.1Rzn>/Mthfd1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	23704330
MGI:5521297	M	MP:0008280	abnormal male germ cell apoptosis	Piwil2<tm2.1Doca>/Piwil2<tm2.1Doca>,Tg(Stra8-icre)1Reb/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * FVB/NJ	N	23706823
MGI:5521297	M	MP:0005621	abnormal cell physiology	Piwil2<tm2.1Doca>/Piwil2<tm2.1Doca>,Tg(Stra8-icre)1Reb/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * FVB/NJ	N	23706823
MGI:5521297	M	MP:0001925	male infertility	Piwil2<tm2.1Doca>/Piwil2<tm2.1Doca>,Tg(Stra8-icre)1Reb/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * FVB/NJ	N	23706823
MGI:5521297	M	MP:0004852	decreased testis weight	Piwil2<tm2.1Doca>/Piwil2<tm2.1Doca>,Tg(Stra8-icre)1Reb/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * FVB/NJ	N	23706823
MGI:5521299	M	MP:0005621	abnormal cell physiology	Piwil2<tm1.1Doca>/Piwil2<tm2.1Doca>,Tg(Stra8-icre)1Reb/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * FVB/NJ	N	23706823
MGI:5521299	M	MP:0004852	decreased testis weight	Piwil2<tm1.1Doca>/Piwil2<tm2.1Doca>,Tg(Stra8-icre)1Reb/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * FVB/NJ	N	23706823
MGI:5521299	M	MP:0008280	abnormal male germ cell apoptosis	Piwil2<tm1.1Doca>/Piwil2<tm2.1Doca>,Tg(Stra8-icre)1Reb/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * FVB/NJ	N	23706823
MGI:5521299	M	MP:0001925	male infertility	Piwil2<tm1.1Doca>/Piwil2<tm2.1Doca>,Tg(Stra8-icre)1Reb/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * FVB/NJ	N	23706823
MGI:5521300	M	MP:0006378	abnormal spermatogonia morphology	Piwil2<tm2.2Doca>/Piwil2<tm2.2Doca>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * BALB/cJ * C57BL/6J	N	23706823
MGI:5521300	M	MP:0005621	abnormal cell physiology	Piwil2<tm2.2Doca>/Piwil2<tm2.2Doca>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * BALB/cJ * C57BL/6J	N	23706823
MGI:5521300	M	MP:0006379	abnormal spermatocyte morphology	Piwil2<tm2.2Doca>/Piwil2<tm2.2Doca>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * BALB/cJ * C57BL/6J	N	23706823
MGI:5521335	M	MP:0002108	abnormal muscle morphology	Dmd<mdx>/Y,Foxn1<nu>/Foxn1<nu>	involves: C57BL/10ScSn	N	15694130
MGI:5521335	M	MP:0009400	decreased skeletal muscle fiber size	Dmd<mdx>/Y,Foxn1<nu>/Foxn1<nu>	involves: C57BL/10ScSn	N	15694130
MGI:5521335	M	MP:0009399	increased skeletal muscle fiber size	Dmd<mdx>/Y,Foxn1<nu>/Foxn1<nu>	involves: C57BL/10ScSn	N	15694130
MGI:5521336	M	MP:0002773	decreased circulating luteinizing hormone level	Foxn1<nu>/Foxn1<nu>	involves: CD-1	N	11259083
MGI:5521336	M	MP:0000705	athymia	Foxn1<nu>/Foxn1<nu>	involves: CD-1	N	11259083
MGI:5521336	M	MP:0005379	endocrine/exocrine gland phenotype	Foxn1<nu>/Foxn1<nu>	involves: CD-1	Y	11259083
MGI:5521336	M	MP:0003361	abnormal circulating gonadotropin level	Foxn1<nu>/Foxn1<nu>	involves: CD-1	N	11259083
MGI:5521336	M	MP:0002790	decreased circulating follicle stimulating hormone level	Foxn1<nu>/Foxn1<nu>	involves: CD-1	N	11259083
MGI:5521490	M	MP:0002176	increased brain weight	Selenbp1<tm1Hyama>/Selenbp1<tm1Hyama>	C57BL/6-Selenbp1<tm1Hyama>	N	23500078
MGI:5521490	M	MP:0004955	increased thymus weight	Selenbp1<tm1Hyama>/Selenbp1<tm1Hyama>	C57BL/6-Selenbp1<tm1Hyama>	N	23500078
MGI:5521490	M	MP:0004953	decreased spleen weight	Selenbp1<tm1Hyama>/Selenbp1<tm1Hyama>	C57BL/6-Selenbp1<tm1Hyama>	N	23500078
MGI:5521490	F	MP:0002682	decreased mature ovarian follicle number	Selenbp1<tm1Hyama>/Selenbp1<tm1Hyama>	C57BL/6-Selenbp1<tm1Hyama>	N	23500078
MGI:5521490	M	MP:0002965	increased circulating serum albumin level	Selenbp1<tm1Hyama>/Selenbp1<tm1Hyama>	C57BL/6-Selenbp1<tm1Hyama>	N	23500078
MGI:5521529	M	MP:0000609	abnormal liver physiology	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0002628	hepatic steatosis	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0000063	decreased bone mineral density	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0011941	increased fluid intake	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0004889	increased energy expenditure	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0010771	integument phenotype	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	Y	23700488
MGI:5521529	M	MP:0001860	liver inflammation	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0011939	increased food intake	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0005178	increased circulating cholesterol level	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0002727	decreased circulating insulin level	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0002981	increased liver weight	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0004952	increased spleen weight	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0000611	jaundice	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0010124	decreased bone mineral content	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0009133	decreased white fat cell size	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0004789	increased bile salt level	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0002941	increased circulating alanine transaminase level	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0008988	abnormal liver perisinusoidal space morphology	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0008989	abnormal liver sinusoid morphology	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0001262	decreased body weight	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0009289	decreased epididymal fat pad weight	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0009295	decreased interscapular fat pad weight	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0010025	decreased total body fat amount	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0009305	decreased retroperitoneal fat pad weight	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0005378	growth/size/body region phenotype	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	Y	23700488
MGI:5521529	M	MP:0009342	enlarged gallbladder	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0031236	increased cecum weight	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0005376	homeostasis/metabolism phenotype	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	Y	23700488
MGI:5521529	M	MP:0005293	impaired glucose tolerance	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0009355	increased liver triglyceride level	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0003103	liver degeneration	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0005560	decreased circulating glucose level	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0002702	decreased circulating free fatty acids level	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521529	M	MP:0005344	increased circulating bilirubin level	Nr1h4<tm1.1Mbj>/Nr1h4<tm1.1Mbj>	B6N.B6-Nr1h4<tm1.1Mbj>	N	23700488
MGI:5521579	M	MP:0009452	abnormal synaptonemal complex	Tdrkh<tm1.2Hfl>/Tdrkh<tm1.2Hfl>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	23714778
MGI:5521579	M	MP:0003205	testicular atrophy	Tdrkh<tm1.2Hfl>/Tdrkh<tm1.2Hfl>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	23714778
MGI:5521579	M	MP:0008877	abnormal DNA methylation	Tdrkh<tm1.2Hfl>/Tdrkh<tm1.2Hfl>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	23714778
MGI:5521579	M	MP:0001925	male infertility	Tdrkh<tm1.2Hfl>/Tdrkh<tm1.2Hfl>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	23714778
MGI:5521579	M	MP:0008261	arrest of male meiosis	Tdrkh<tm1.2Hfl>/Tdrkh<tm1.2Hfl>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	23714778
MGI:5521579	M	MP:0010948	abnormal double-strand DNA break repair	Tdrkh<tm1.2Hfl>/Tdrkh<tm1.2Hfl>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	23714778
MGI:5521579	M	MP:0001147	small testis	Tdrkh<tm1.2Hfl>/Tdrkh<tm1.2Hfl>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	23714778
MGI:5521579	M	MP:0005621	abnormal cell physiology	Tdrkh<tm1.2Hfl>/Tdrkh<tm1.2Hfl>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	23714778
MGI:5521579	M	MP:0005159	azoospermia	Tdrkh<tm1.2Hfl>/Tdrkh<tm1.2Hfl>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	23714778
MGI:5522556	M	MP:0012307	impaired spatial learning	Dgcr8<Gt(XG058)Byg>/Dgcr8<+>	involves: 129P2/OlaHsd * C57BL/6	N	23719809
MGI:5522556	M	MP:0002573	behavioral despair	Dgcr8<Gt(XG058)Byg>/Dgcr8<+>	involves: 129P2/OlaHsd * C57BL/6	N	23719809
MGI:5522556	M	MP:0008428	abnormal spatial working memory	Dgcr8<Gt(XG058)Byg>/Dgcr8<+>	involves: 129P2/OlaHsd * C57BL/6	N	23719809
MGI:5522834	M	MP:0005389	reproductive system phenotype	Tubb2b<brdp>/Tubb2b<+>	involves: A/J * FVB	Y	23727838
MGI:5522965	F	MP:0001119	abnormal female reproductive system morphology	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522965	M	MP:0001925	male infertility	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522965	F	MP:0009094	abnormal endometrial gland morphology	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522965	M	MP:0004930	small epididymis	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522965	M	MP:0009205	abnormal internal male genitalia morphology	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522965	F	MP:0009209	abnormal internal female genitalia morphology	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522965	F	MP:0009081	thin uterus	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522965	M	MP:0031287	bilateral cryptorchism	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522965	F	MP:0001120	abnormal uterus morphology	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522965	F	MP:0008257	thin myometrium	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522965	M	MP:0002769	abnormal vas deferens morphology	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522965	F	MP:0001926	female infertility	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522965	M	MP:0002662	abnormal cauda epididymis morphology	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522965	M	MP:0001156	abnormal spermatogenesis	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522969	M	MP:0002769	abnormal vas deferens morphology	Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522969	F	MP:0005389	reproductive system phenotype	Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	Y	23760953
MGI:5522969	M	MP:0001925	male infertility	Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522969	M	MP:0030983	failure of copulatory plug deposition	Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522969	F	MP:0001923	reduced female fertility	Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522969	F	MP:0001935	decreased litter size	Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522978	F	MP:0001935	decreased litter size	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<+>	involves: 129 * CD-1	N	23760953
MGI:5522978	F	MP:0001926	female infertility	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<+>	involves: 129 * CD-1	N	23760953
MGI:5522978	F	MP:0009209	abnormal internal female genitalia morphology	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<+>	involves: 129 * CD-1	N	23760953
MGI:5522978	F	MP:0001923	reduced female fertility	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<+>	involves: 129 * CD-1	N	23760953
MGI:5522978	M	MP:0002769	abnormal vas deferens morphology	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<+>	involves: 129 * CD-1	N	23760953
MGI:5522979	F	MP:0009081	thin uterus	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522979	M	MP:0002769	abnormal vas deferens morphology	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522979	M	MP:0004930	small epididymis	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522979	F	MP:0001926	female infertility	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522979	M	MP:0001146	abnormal testis morphology	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522979	M	MP:0002662	abnormal cauda epididymis morphology	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522979	F	MP:0001120	abnormal uterus morphology	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522979	M	MP:0031286	unilateral cryptorchism	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522979	F	MP:0008257	thin myometrium	Hoxa<tm1.1Ssp>/Hoxa<+>,Hoxd<tm1.1Ssp>/Hoxd<tm1.1Ssp>	involves: 129 * CD-1	N	23760953
MGI:5522980	M	MP:0002769	abnormal vas deferens morphology	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>,Hoxd<tm1.1Ssp>/Hoxd<+>	involves: 129 * CD-1	N	23760953
MGI:5522980	F	MP:0008257	thin myometrium	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>,Hoxd<tm1.1Ssp>/Hoxd<+>	involves: 129 * CD-1	N	23760953
MGI:5522980	F	MP:0009081	thin uterus	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>,Hoxd<tm1.1Ssp>/Hoxd<+>	involves: 129 * CD-1	N	23760953
MGI:5522980	M	MP:0002662	abnormal cauda epididymis morphology	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>,Hoxd<tm1.1Ssp>/Hoxd<+>	involves: 129 * CD-1	N	23760953
MGI:5522980	F	MP:0001926	female infertility	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>,Hoxd<tm1.1Ssp>/Hoxd<+>	involves: 129 * CD-1	N	23760953
MGI:5522980	M	MP:0001925	male infertility	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>,Hoxd<tm1.1Ssp>/Hoxd<+>	involves: 129 * CD-1	N	23760953
MGI:5522980	M	MP:0004930	small epididymis	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>,Hoxd<tm1.1Ssp>/Hoxd<+>	involves: 129 * CD-1	N	23760953
MGI:5522980	F	MP:0001120	abnormal uterus morphology	Hoxa<tm1.1Ssp>/Hoxa<tm1.1Ssp>,Hoxd<tm1.1Ssp>/Hoxd<+>	involves: 129 * CD-1	N	23760953
MGI:5523090	M	MP:0002628	hepatic steatosis	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0010359	increased liver free fatty acids level	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0003674	oxidative stress	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0009355	increased liver triglyceride level	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0005376	homeostasis/metabolism phenotype	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	Y	23733885
MGI:5523090	M	MP:0011582	decreased triglyceride lipase activity	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0010027	increased liver cholesterol level	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0000598	abnormal liver morphology	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0001547	abnormal lipid level	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0001860	liver inflammation	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0014172	decreased fatty acid oxidation	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0000609	abnormal liver physiology	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0000599	enlarged liver	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0003333	liver fibrosis	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0004777	abnormal phospholipid level	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0002941	increased circulating alanine transaminase level	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0005343	increased circulating aspartate transaminase level	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0002981	increased liver weight	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0000603	pale liver	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523090	M	MP:0000607	abnormal hepatocyte morphology	Abhd5<tm1.1Lqyu>/Abhd5<tm1.1Lqyu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA	N	23733885
MGI:5523417	M	MP:0002169	no abnormal phenotype detected	Porcn<tm1.1Jrt>/Y	B6.Cg-Porcn<tm1.1Jrt>	N	23760955
MGI:5523420	F	MP:0002169	no abnormal phenotype detected	Porcn<tm1.1Jrt>/Porcn<+>	B6.Cg-Porcn<tm1.1Jrt>	N	23760955
MGI:5523422	M	MP:0002169	no abnormal phenotype detected	Porcn<tm1.1Jrt>/Y	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	N	23760955
MGI:5523424	F	MP:0002169	no abnormal phenotype detected	Porcn<tm1.1Jrt>/Porcn<+>	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	N	23760955
MGI:5523428	M	MP:0002086	abnormal extraembryonic tissue morphology	Porcn<tm1.1Jrt>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	N	23760955
MGI:5523428	M	MP:0009593	absent chorion	Porcn<tm1.1Jrt>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	N	23760955
MGI:5523428	M	MP:0001698	decreased embryo size	Porcn<tm1.1Jrt>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	N	23760955
MGI:5523428	M	MP:0005030	absent amnion	Porcn<tm1.1Jrt>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	N	23760955
MGI:5523428	M	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance	Porcn<tm1.1Jrt>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	N	23760955
MGI:5523429	F	MP:0001672	abnormal embryo development	Porcn<tm1.1Jrt>/Porcn<+>,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	N	23760955
MGI:5523429	F	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Porcn<tm1.1Jrt>/Porcn<+>,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	N	23760955
MGI:5523429	F	MP:0005380	embryo phenotype	Porcn<tm1.1Jrt>/Porcn<+>,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	Y	23760955
MGI:5523429	F	MP:0001725	abnormal umbilical cord morphology	Porcn<tm1.1Jrt>/Porcn<+>,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	N	23760955
MGI:5523429	F	MP:0003631	nervous system phenotype	Porcn<tm1.1Jrt>/Porcn<+>,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	Y	23760955
MGI:5523429	F	MP:0001726	abnormal allantois morphology	Porcn<tm1.1Jrt>/Porcn<+>,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	N	23760955
MGI:5523429	F	MP:0001711	abnormal placenta morphology	Porcn<tm1.1Jrt>/Porcn<+>,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCr * ICR	N	23760955
MGI:5523430	F	MP:0010768	mortality/aging	Porcn<tm1.1Jrt>/Porcn<+>,Tg(Ttr-cre)1Hadj/0	involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCr * CBA/J	Y	23760955
MGI:5523431	F	MP:0005380	embryo phenotype	Porcn<tm1.1Jrt>/Porcn<+>,Tg(CAG-EGFP)D4Nagy/0,Tg(Zp3-cre)3Mrt/0	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6J * C57BL/6NCr * FVB/N	Y	23760955
MGI:5523432	M	MP:0001696	failure to gastrulate	Porcn<tm1.1Jrt>/Y,Tg(CAG-EGFP)D4Nagy/0,Tg(Zp3-cre)3Mrt/0	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6J * C57BL/6NCr * FVB/N	N	23760955
MGI:5523454	M	MP:0005658	increased susceptibility to diet-induced obesity	Gt(ROSA)26Sor<tm1(HBEGF)Awai>/Gt(ROSA)26Sor<tm9(CAG-tdTomato)Hze>,Oxt<tm1.1(cre)Dolsn>/Oxt<+>	involves: 129S6/SvEvTac * C57BL/6	N	23028821
MGI:5523484	M	MP:0005169	abnormal male meiosis	Exo1<tm2Wed>/Exo1<tm2Wed>	involves: 129 * C57BL/6	N	23754438
MGI:5523484	F	MP:0005389	reproductive system phenotype	Exo1<tm2Wed>/Exo1<tm2Wed>	involves: 129 * C57BL/6	Y	23754438
MGI:5523484	M	MP:0004852	decreased testis weight	Exo1<tm2Wed>/Exo1<tm2Wed>	involves: 129 * C57BL/6	N	23754438
MGI:5523484	M	MP:0008280	abnormal male germ cell apoptosis	Exo1<tm2Wed>/Exo1<tm2Wed>	involves: 129 * C57BL/6	N	23754438
MGI:5523484	M	MP:0001147	small testis	Exo1<tm2Wed>/Exo1<tm2Wed>	involves: 129 * C57BL/6	N	23754438
MGI:5523484	M	MP:0002687	oligozoospermia	Exo1<tm2Wed>/Exo1<tm2Wed>	involves: 129 * C57BL/6	N	23754438
MGI:5523548	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Spo11<tm1Bdm>/Spo11<tm1Bdm>	involves: 129	N	23754961
MGI:5523548	F	MP:0001926	female infertility	Spo11<tm1Bdm>/Spo11<tm1Bdm>	involves: 129	N	23754961
MGI:5523548	M	MP:0001925	male infertility	Spo11<tm1Bdm>/Spo11<tm1Bdm>	involves: 129	N	23754961
MGI:5523548	M	MP:0001155	arrest of spermatogenesis	Spo11<tm1Bdm>/Spo11<tm1Bdm>	involves: 129	N	23754961
MGI:5523548	F	MP:0001931	abnormal oogenesis	Spo11<tm1Bdm>/Spo11<tm1Bdm>	involves: 129	N	23754961
MGI:5523548	M	MP:0010948	abnormal double-strand DNA break repair	Spo11<tm1Bdm>/Spo11<tm1Bdm>	involves: 129	N	23754961
MGI:5523608	M	MP:0001147	small testis	Ar<em1Liuy>/Y	involves: C57BL/6J * CBA	N	23759306
MGI:5523608	M	MP:0001939	secondary sex reversal	Ar<em1Liuy>/Y	involves: C57BL/6J * CBA	N	23759306
MGI:5523867	F	MP:0005431	decreased oocyte number	Mir200b<tm1.1Osb>/Mir200b<tm1.1Osb>,Mir429<m1Osb>/Mir429<m1Osb>	involves: 129S2/SvPas * C57BL/6	N	23765281
MGI:5523867	F	MP:0001923	reduced female fertility	Mir200b<tm1.1Osb>/Mir200b<tm1.1Osb>,Mir429<m1Osb>/Mir429<m1Osb>	involves: 129S2/SvPas * C57BL/6	N	23765281
MGI:5523867	F	MP:0002773	decreased circulating luteinizing hormone level	Mir200b<tm1.1Osb>/Mir200b<tm1.1Osb>,Mir429<m1Osb>/Mir429<m1Osb>	involves: 129S2/SvPas * C57BL/6	N	23765281
MGI:5523867	M	MP:0005389	reproductive system phenotype	Mir200b<tm1.1Osb>/Mir200b<tm1.1Osb>,Mir429<m1Osb>/Mir429<m1Osb>	involves: 129S2/SvPas * C57BL/6	Y	23765281
MGI:5523867	F	MP:0009017	prolonged estrus	Mir200b<tm1.1Osb>/Mir200b<tm1.1Osb>,Mir429<m1Osb>/Mir429<m1Osb>	involves: 129S2/SvPas * C57BL/6	N	23765281
MGI:5523867	F	MP:0005132	decreased luteinizing hormone level	Mir200b<tm1.1Osb>/Mir200b<tm1.1Osb>,Mir429<m1Osb>/Mir429<m1Osb>	involves: 129S2/SvPas * C57BL/6	N	23765281
MGI:5523867	F	MP:0005185	decreased circulating progesterone level	Mir200b<tm1.1Osb>/Mir200b<tm1.1Osb>,Mir429<m1Osb>/Mir429<m1Osb>	involves: 129S2/SvPas * C57BL/6	N	23765281
MGI:5523867	F	MP:0001935	decreased litter size	Mir200b<tm1.1Osb>/Mir200b<tm1.1Osb>,Mir429<m1Osb>/Mir429<m1Osb>	involves: 129S2/SvPas * C57BL/6	N	23765281
MGI:5523867	F	MP:0003355	decreased ovulation rate	Mir200b<tm1.1Osb>/Mir200b<tm1.1Osb>,Mir429<m1Osb>/Mir429<m1Osb>	involves: 129S2/SvPas * C57BL/6	N	23765281
MGI:5523867	F	MP:0002680	decreased corpora lutea number	Mir200b<tm1.1Osb>/Mir200b<tm1.1Osb>,Mir429<m1Osb>/Mir429<m1Osb>	involves: 129S2/SvPas * C57BL/6	N	23765281
MGI:5523950	F	MP:0001923	reduced female fertility	Hsd17b4<tm2Baes>/Hsd17b4<tm2Baes>,Tg(Nes-cre)1Kln/0	involves: 129 * C57BL/6 * SJL	N	23777740
MGI:5523950	M	MP:0001925	male infertility	Hsd17b4<tm2Baes>/Hsd17b4<tm2Baes>,Tg(Nes-cre)1Kln/0	involves: 129 * C57BL/6 * SJL	N	23777740
MGI:5523950	F	MP:0001935	decreased litter size	Hsd17b4<tm2Baes>/Hsd17b4<tm2Baes>,Tg(Nes-cre)1Kln/0	involves: 129 * C57BL/6 * SJL	N	23777740
MGI:5523971	M	MP:0001922	reduced male fertility	Kit<Wps>/Kit<Wps>	involves: C57BL/6J * CBA/CaJ	N	20095975
MGI:5523971	F	MP:0001923	reduced female fertility	Kit<Wps>/Kit<Wps>	involves: C57BL/6J * CBA/CaJ	N	20095975
MGI:5524001	M	MP:0001925	male infertility	Pla2g6<tm1Zyao>/Pla2g6<tm1Zyao>	involves: 129S6/SvEvTac * C57BL/6	N	25337551
MGI:5524001	M	MP:0010331	abnormal apolipoprotein level	Pla2g6<tm1Zyao>/Pla2g6<tm1Zyao>	involves: 129S6/SvEvTac * C57BL/6	N	25337551
MGI:5524001	F	MP:0002001	blindness	Pla2g6<tm1Zyao>/Pla2g6<tm1Zyao>	involves: 129S6/SvEvTac * C57BL/6	N	25337551
MGI:5524040	F	MP:0005389	reproductive system phenotype	Nhlh2<tm2Thbr>/Nhlh2<tm2Thbr>,Tg(Pomc-EGFP)1Low/0,Tg(Pomc1-cre)16Lowl/0	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * FVB/N	Y	23785158
MGI:5524041	F	MP:0005389	reproductive system phenotype	Nhlh2<tm2Thbr>/Nhlh2<tm2Thbr>,Tg(Agrp-cre)1Gsb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	Y	23785158
MGI:5524042	F	MP:0005389	reproductive system phenotype	Kiss1<tm1.1(cre)Uboe>/Kiss1<+>,Nhlh2<tm2Thbr>/Nhlh2<tm2Thbr>	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * C57BL/6J	Y	23785158
MGI:5524043	F	MP:0005181	decreased circulating estradiol level	Nhlh2<tm2Thbr>/Nhlh2<tm2Thbr>,Tg(CMV-cre)1Cgn/0	involves: 129S7/SvEvBrd * BALB/cJ * C57BL/6	N	23785158
MGI:5524043	F	MP:0004905	decreased uterus weight	Nhlh2<tm2Thbr>/Nhlh2<tm2Thbr>,Tg(CMV-cre)1Cgn/0	involves: 129S7/SvEvBrd * BALB/cJ * C57BL/6	N	23785158
MGI:5524044	F	MP:0011723	ectopic neuron	Nhlh2<tm1Thbr>/Nhlh2<tm1Thbr>,Tg(Pomc-EGFP)1Low/0	involves: 129S4/SvJae * C57BL/6J	N	23785158
MGI:5524044	F	MP:0008947	increased neuron number	Nhlh2<tm1Thbr>/Nhlh2<tm1Thbr>,Tg(Pomc-EGFP)1Low/0	involves: 129S4/SvJae * C57BL/6J	N	23785158
MGI:5524046	F	MP:0005376	homeostasis/metabolism phenotype	Nhlh2<tm2Thbr>/Nhlh2<tm2Thbr>,Tg(Gnrh1-cre)1Dlc/0,Tg(Pomc-EGFP)1Low/0	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * CBA	Y	23785158
MGI:5524047	F	MP:0001127	small ovary	Gt(ROSA)26Sor<tm1(DTA)Riet>/Gt(ROSA)26Sor<+>,Tg(Pomc-EGFP)1Low/0,Tg(Gnrh1-cre)1Dlc/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA	N	23785158
MGI:5524047	F	MP:0004905	decreased uterus weight	Gt(ROSA)26Sor<tm1(DTA)Riet>/Gt(ROSA)26Sor<+>,Tg(Pomc-EGFP)1Low/0,Tg(Gnrh1-cre)1Dlc/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA	N	23785158
MGI:5524278	M	MP:0031365	prostate gland ventral lobe hyperplasia	Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>/Gt(ROSA)26Sor<+>,Tg(Pbsn-cre)4Prb/0	involves: 129 * C57BL/6 * DBA/2	N	23817021
MGI:5524279	M	MP:0031365	prostate gland ventral lobe hyperplasia	Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>/Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>,Tg(Pbsn-cre)4Prb/0	involves: 129 * C57BL/6 * DBA/2	N	23817021
MGI:5524280	M	MP:0004958	enlarged prostate gland	Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>/Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	23817021
MGI:5524280	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>/Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	23817021
MGI:5524280	M	MP:0001270	distended abdomen	Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>/Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	23817021
MGI:5524280	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>/Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	23817021
MGI:5524280	M	MP:0003607	abnormal prostate gland physiology	Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>/Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	23817021
MGI:5524280	M	MP:0002083	premature death	Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>/Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	23817021
MGI:5524280	M	MP:0009105	penis prolapse	Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>/Gt(ROSA)26Sor<tm1(TMPRSS2/ERG)Key>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	23817021
MGI:5524975	M	MP:0002675	asthenozoospermia	Gt(ROSA)26Sor<tm1.1(Sstr3/GFP)Bky>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac * FVB/N	N	23819925
MGI:5524975	F	MP:0005389	reproductive system phenotype	Gt(ROSA)26Sor<tm1.1(Sstr3/GFP)Bky>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac * FVB/N	Y	23819925
MGI:5524975	M	MP:0001925	male infertility	Gt(ROSA)26Sor<tm1.1(Sstr3/GFP)Bky>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac * FVB/N	N	23819925
MGI:5524975	M	MP:0009243	hairpin sperm flagellum	Gt(ROSA)26Sor<tm1.1(Sstr3/GFP)Bky>/Gt(ROSA)26Sor<+>	involves: C57BL/6 * C57BL/6NTac * FVB/N	N	23819925
MGI:5526018	F	MP:0000063	decreased bone mineral density	Abcb4<tm1Bor>/Abcb4<tm1Bor>	C.129P2-Abcb4<tm1Bor>	N	23545228
MGI:5526018	F	MP:0003797	abnormal compact bone morphology	Abcb4<tm1Bor>/Abcb4<tm1Bor>	C.129P2-Abcb4<tm1Bor>	N	23545228
MGI:5526018	F	MP:0020010	decreased bone mineral density of femur	Abcb4<tm1Bor>/Abcb4<tm1Bor>	C.129P2-Abcb4<tm1Bor>	N	23545228
MGI:5526029	M	MP:0004733	abnormal thoracic cavity morphology	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0001633	poor circulation	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0003915	increased heart left ventricle weight	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0000274	enlarged heart	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0004215	abnormal myocardial fiber physiology	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0003711	pathological neovascularization	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0001853	heart inflammation	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0002953	thick ventricular wall	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0002833	increased heart weight	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0001175	abnormal lung morphology	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0001625	cardiac hypertrophy	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0001855	abnormal atrial thrombosis	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0004231	abnormal calcium ion homeostasis	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0006138	congestive heart failure	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0005385	cardiovascular system phenotype	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	Y	24082121
MGI:5526029	M	MP:0031633	decreased heart left ventricle muscle contractility	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0003141	cardiac fibrosis	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0002753	dilated heart left ventricle	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0011925	abnormal heart echocardiography feature	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526029	M	MP:0004564	increased myocardial fiber size	Nr3c1<tm1.1Jaci>/Nr3c1<tm1.1Jaci>,Tg(Myh6-cre)2182Mds/0	involves: C57BL/6 * FVB/N	N	24082121
MGI:5526066	M	MP:0003962	abnormal adrenaline level	Mrap2<tm1.1Maj>/Mrap2<tm1.1Maj>	either: B6.129-Mrap2<tm1.1Maj> or (involves: 129 * 129S6/SvEvTac)	N	23869016
MGI:5526066	M	MP:0003964	abnormal noradrenaline level	Mrap2<tm1.1Maj>/Mrap2<tm1.1Maj>	either: B6.129-Mrap2<tm1.1Maj> or (involves: 129 * 129S6/SvEvTac)	N	23869016
MGI:5526095	F	MP:0002439	abnormal plasma cell morphology	Jak1<M1Mhda>/Jak1<+>	C3HeB/FeJ-Jak1<M1Mhda>	N	23791841
MGI:5526095	M	MP:0000194	increased circulating calcium level	Jak1<M1Mhda>/Jak1<+>	C3HeB/FeJ-Jak1<M1Mhda>	N	23791841
MGI:5526095	F	MP:0005419	decreased circulating serum albumin level	Jak1<M1Mhda>/Jak1<+>	C3HeB/FeJ-Jak1<M1Mhda>	N	23791841
MGI:5526095	F	MP:0000414	alopecia	Jak1<M1Mhda>/Jak1<+>	C3HeB/FeJ-Jak1<M1Mhda>	N	23791841
MGI:5526095	F	MP:0000691	enlarged spleen	Jak1<M1Mhda>/Jak1<+>	C3HeB/FeJ-Jak1<M1Mhda>	N	23791841
MGI:5526972	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-PIK3CA*H1047R,-luc)2239Jjz/0	involves: FVB/N	N	21822287
MGI:5526972	F	MP:0010299	increased mammary gland tumor incidence	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-PIK3CA*H1047R,-luc)2239Jjz/0	involves: FVB/N	N	21822287
MGI:5526996	M	MP:0001661	extended life span	Tg(Prnp-TARDBP*A315T)95Balo/0	(FVB/NJ x B6.Cg-Tg(Prnp-TARDBP*A315T)95Balo/J)F1	N	24141148
MGI:5526997	M	MP:0001661	extended life span	Tg(Prnp-TARDBP*A315T)95Balo/0	(ALR/LtJ x B6.Cg-Tg(Prnp-TARDBP*A315T)95Balo/J)F1	N	24141148
MGI:5526998	M	MP:0001661	extended life span	Tg(Prnp-TARDBP*A315T)95Balo/0	(129S1/SvImJ x B6.Cg-Tg(Prnp-TARDBP*A315T)95Balo/J)F1	N	24141148
MGI:5526999	M	MP:0001661	extended life span	Tg(Prnp-TARDBP*A315T)95Balo/0	(PWK/PhJ x B6.Cg-Tg(Prnp-TARDBP*A315T)95Balo/J)F1	N	24141148
MGI:5527000	M	MP:0001661	extended life span	Tg(Prnp-TARDBP*A315T)95Balo/0	(WSB/EiJ x B6.Cg-Tg(Prnp-TARDBP*A315T)95Balo/J)F1	N	24141148
MGI:5527001	M	MP:0001661	extended life span	Tg(Prnp-TARDBP*A315T)95Balo/0	(C3H/HeJ x B6.Cg-Tg(Prnp-TARDBP*A315T)95Balo/J)F1	N	24141148
MGI:5527002	M	MP:0000938	motor neuron degeneration	Tg(Prnp-TARDBP*A315T)95Balo/0	B6.Cg-Tg(Prnp-TARDBP*A315T)95Balo/J	N	24141148
MGI:5527002	M	MP:0000937	abnormal motor neuron morphology	Tg(Prnp-TARDBP*A315T)95Balo/0	B6.Cg-Tg(Prnp-TARDBP*A315T)95Balo/J	N	24141148
MGI:5527002	M	MP:0001405	impaired coordination	Tg(Prnp-TARDBP*A315T)95Balo/0	B6.Cg-Tg(Prnp-TARDBP*A315T)95Balo/J	N	24141148
MGI:5527002	M	MP:0011975	neuronal cytoplasmic inclusions	Tg(Prnp-TARDBP*A315T)95Balo/0	B6.Cg-Tg(Prnp-TARDBP*A315T)95Balo/J	N	24141148
MGI:5527002	M	MP:0005404	abnormal axon morphology	Tg(Prnp-TARDBP*A315T)95Balo/0	B6.Cg-Tg(Prnp-TARDBP*A315T)95Balo/J	N	24141148
MGI:5527002	M	MP:0003354	astrocytosis	Tg(Prnp-TARDBP*A315T)95Balo/0	B6.Cg-Tg(Prnp-TARDBP*A315T)95Balo/J	N	24141148
MGI:5527317	F	MP:0013446	enlarged Harderian gland	Tg(MMTV-ERBB2)5Erick/?	FVB/N-Tg(MMTV-ERBB2)5Erick	N	15073130
MGI:5527317	F	MP:0001272	increased metastatic potential	Tg(MMTV-ERBB2)5Erick/?	FVB/N-Tg(MMTV-ERBB2)5Erick	N	15073130
MGI:5527317	F	MP:0013538	increased Harderian gland adenoma incidence	Tg(MMTV-ERBB2)5Erick/?	FVB/N-Tg(MMTV-ERBB2)5Erick	N	15073130
MGI:5527317	F	MP:0010299	increased mammary gland tumor incidence	Tg(MMTV-ERBB2)5Erick/?	FVB/N-Tg(MMTV-ERBB2)5Erick	N	15073130
MGI:5527317	F	MP:0002750	exophthalmos	Tg(MMTV-ERBB2)5Erick/?	FVB/N-Tg(MMTV-ERBB2)5Erick	N	15073130
MGI:5527317	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-ERBB2)5Erick/?	FVB/N-Tg(MMTV-ERBB2)5Erick	N	15073130
MGI:5527391	F	MP:0004955	increased thymus weight	Bok<tm1.1Ast>/Bok<tm1.1Ast>	involves: BALB/cJ * C57BL/6	N	22281706
MGI:5527391	F	MP:0004952	increased spleen weight	Bok<tm1.1Ast>/Bok<tm1.1Ast>	involves: BALB/cJ * C57BL/6	N	22281706
MGI:5527455	M	MP:0003017	decreased circulating bicarbonate level	Mmut<tm1Cpv>/Mmut<tm1Cpv>,Tg(Alb-Mut)#Cpv/0	involves: C57BL/6	N	23898205
MGI:5527455	F	MP:0011635	abnormal mitochondrial crista morphology	Mmut<tm1Cpv>/Mmut<tm1Cpv>,Tg(Alb-Mut)#Cpv/0	involves: C57BL/6	N	23898205
MGI:5527455	F	MP:0002152	abnormal brain morphology	Mmut<tm1Cpv>/Mmut<tm1Cpv>,Tg(Alb-Mut)#Cpv/0	involves: C57BL/6	N	23898205
MGI:5527455	F	MP:0011405	tubulointerstitial nephritis	Mmut<tm1Cpv>/Mmut<tm1Cpv>,Tg(Alb-Mut)#Cpv/0	involves: C57BL/6	N	23898205
MGI:5527455	M	MP:0003019	increased circulating chloride level	Mmut<tm1Cpv>/Mmut<tm1Cpv>,Tg(Alb-Mut)#Cpv/0	involves: C57BL/6	N	23898205
MGI:5527455	M	MP:0012551	metabolic acidosis	Mmut<tm1Cpv>/Mmut<tm1Cpv>,Tg(Alb-Mut)#Cpv/0	involves: C57BL/6	N	23898205
MGI:5527455	F	MP:0001263	weight loss	Mmut<tm1Cpv>/Mmut<tm1Cpv>,Tg(Alb-Mut)#Cpv/0	involves: C57BL/6	N	23898205
MGI:5527455	M	MP:0005553	increased circulating creatinine level	Mmut<tm1Cpv>/Mmut<tm1Cpv>,Tg(Alb-Mut)#Cpv/0	involves: C57BL/6	N	23898205
MGI:5527455	F	MP:0002135	abnormal kidney morphology	Mmut<tm1Cpv>/Mmut<tm1Cpv>,Tg(Alb-Mut)#Cpv/0	involves: C57BL/6	N	23898205
MGI:5527455	F	MP:0011637	abnormal mitochondrial matrix morphology	Mmut<tm1Cpv>/Mmut<tm1Cpv>,Tg(Alb-Mut)#Cpv/0	involves: C57BL/6	N	23898205
MGI:5527455	F	MP:0005370	liver/biliary system phenotype	Mmut<tm1Cpv>/Mmut<tm1Cpv>,Tg(Alb-Mut)#Cpv/0	involves: C57BL/6	Y	23898205
MGI:5528467	M	MP:0000558	abnormal tibia morphology	Chst14<tm1.1Msch>/Chst14<tm1.1Msch>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23360803
MGI:5528467	M	MP:0003918	decreased kidney weight	Chst14<tm1.1Msch>/Chst14<tm1.1Msch>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23360803
MGI:5528467	M	MP:0003631	nervous system phenotype	Chst14<tm1.1Msch>/Chst14<tm1.1Msch>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	23360803
MGI:5528467	M	MP:0003402	decreased liver weight	Chst14<tm1.1Msch>/Chst14<tm1.1Msch>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23360803
MGI:5528467	M	MP:0002834	decreased heart weight	Chst14<tm1.1Msch>/Chst14<tm1.1Msch>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23360803
MGI:5528706	F	MP:0008976	delayed female fertility	Tg(Amh-SMAD2*)2Tkw/?	involves: CD-1	N	16141389
MGI:5528706	F	MP:0002680	decreased corpora lutea number	Tg(Amh-SMAD2*)2Tkw/?	involves: CD-1	N	16141389
MGI:5528706	F	MP:0001923	reduced female fertility	Tg(Amh-SMAD2*)2Tkw/?	involves: CD-1	N	16141389
MGI:5528706	F	MP:0001126	abnormal ovary morphology	Tg(Amh-SMAD2*)2Tkw/?	involves: CD-1	N	16141389
MGI:5528706	F	MP:0001935	decreased litter size	Tg(Amh-SMAD2*)2Tkw/?	involves: CD-1	N	16141389
MGI:5528706	F	MP:0013609	abnormal ovarian medulla morphology	Tg(Amh-SMAD2*)2Tkw/?	involves: CD-1	N	16141389
MGI:5528706	F	MP:0009433	polyovular ovarian follicle	Tg(Amh-SMAD2*)2Tkw/?	involves: CD-1	N	16141389
MGI:5528706	F	MP:0002016	ovary cyst	Tg(Amh-SMAD2*)2Tkw/?	involves: CD-1	N	16141389
MGI:5528806	M	MP:0001925	male infertility	Atp1a4<tm1Blac>/Atp1a4<tm1Blac>	involves: 129S6/SvEvTac * C57BL/6	N	23229519
MGI:5528806	F	MP:0005389	reproductive system phenotype	Atp1a4<tm1Blac>/Atp1a4<tm1Blac>	involves: 129S6/SvEvTac * C57BL/6	Y	23229519
MGI:5528806	M	MP:0009282	decreased hyperactivated sperm motility	Atp1a4<tm1Blac>/Atp1a4<tm1Blac>	involves: 129S6/SvEvTac * C57BL/6	N	23229519
MGI:5528806	M	MP:0009237	kinked sperm flagellum	Atp1a4<tm1Blac>/Atp1a4<tm1Blac>	involves: 129S6/SvEvTac * C57BL/6	N	23229519
MGI:5528981	F	MP:0002757	decreased vertical activity	Thrb<tm1.1Syc>/Thrb<tm1.1Syc>	involves: 129S6/SvEvTac * NIH Black Swiss	N	15983791
MGI:5528981	M	MP:0011617	abnormal habituation	Thrb<tm1.1Syc>/Thrb<tm1.1Syc>	involves: 129S6/SvEvTac * NIH Black Swiss	N	15983791
MGI:5528982	M	MP:0011617	abnormal habituation	Thrb<tm1.1Syc>/Thrb<+>	involves: 129S6/SvEvTac * NIH Black Swiss	N	15983791
MGI:5528982	M	MP:0012315	impaired learning	Thrb<tm1.1Syc>/Thrb<+>	involves: 129S6/SvEvTac * NIH Black Swiss	N	15983791
MGI:5529018	M	MP:0011628	increased mitochondrial number	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0011631	decreased mitochondrial size	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0011633	abnormal mitochondrial shape	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0002952	ventricular cardiomyopathy	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0005598	decreased heart ventricle muscle contractility	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0010579	increased heart left ventricle size	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0011636	disorganized mitochondrial cristae	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0010392	prolonged QRS complex duration	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0030927	decreased telomere length	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0003674	oxidative stress	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0002753	dilated heart left ventricle	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0003141	cardiac fibrosis	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0002795	dilated cardiomyopathy	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0002083	premature death	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529018	M	MP:0000278	abnormal myocardial fiber morphology	Dmd<mdx-4Cv>/Dmd<mdx-4Cv>,Terc<tm1Rdp>/Terc<tm1Rdp>	B6.Cg-Terc<tm1Rdp> Dmd<mdx-4Cv>	N	23831727
MGI:5529127	F	MP:0002841	impaired skeletal muscle contractility	Mstn<Cmpt>/Mstn<Cmpt>	BEH	N	17267614
MGI:5529272	M	MP:0000063	decreased bone mineral density	Chad<tm1Gast>/Chad<tm1Gast>	B6.129-Chad<tm1Gast>	N	23755099
MGI:5529272	M	MP:0003797	abnormal compact bone morphology	Chad<tm1Gast>/Chad<tm1Gast>	B6.129-Chad<tm1Gast>	N	23755099
MGI:5529272	F	MP:0000130	abnormal trabecular bone morphology	Chad<tm1Gast>/Chad<tm1Gast>	B6.129-Chad<tm1Gast>	N	23755099
MGI:5529272	M	MP:0010025	decreased total body fat amount	Chad<tm1Gast>/Chad<tm1Gast>	B6.129-Chad<tm1Gast>	N	23755099
MGI:5529466	F	MP:0004924	abnormal behavior	Mecp2<tm4.1Bird>/Mecp2<+>	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5529467	F	MP:0004924	abnormal behavior	Mecp2<tm5.1Bird>/Mecp2<+>	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5529468	M	MP:0001513	limb grasping	Mecp2<tm2.1Meg>/Y	involves: 129P2/OlaHsd	N	23770565
MGI:5529468	M	MP:0002083	premature death	Mecp2<tm2.1Meg>/Y	involves: 129P2/OlaHsd	N	23770565
MGI:5529468	M	MP:0001405	impaired coordination	Mecp2<tm2.1Meg>/Y	involves: 129P2/OlaHsd	N	23770565
MGI:5529468	M	MP:0001402	decreased locomotor activity	Mecp2<tm2.1Meg>/Y	involves: 129P2/OlaHsd	N	23770565
MGI:5529468	M	MP:0002175	decreased brain weight	Mecp2<tm2.1Meg>/Y	involves: 129P2/OlaHsd	N	23770565
MGI:5529468	M	MP:0004924	abnormal behavior	Mecp2<tm2.1Meg>/Y	involves: 129P2/OlaHsd	N	23770565
MGI:5529521	M	MP:0012298	hypoactivity in response to feed restriction	Tg(ACTB-THRB*)#Syc/0	involves: CD-1	N	10454355
MGI:5529521	M	MP:0002757	decreased vertical activity	Tg(ACTB-THRB*)#Syc/0	involves: CD-1	N	10454355
MGI:5529521	M	MP:0002574	increased vertical activity	Tg(ACTB-THRB*)#Syc/0	involves: CD-1	N	10454355
MGI:5529521	M	MP:0031391	increased locomotor activity	Tg(ACTB-THRB*)#Syc/0	involves: CD-1	N	10454355
MGI:5529628	M	MP:0009679	abnormal spinal cord ventral column morphology	Dp(XTceal3-Plp1)1Gmh/Y	involves: 129S7/SvEvBrd * C57BL/6	N	23864668
MGI:5529628	M	MP:0011731	decreased myelin sheath thickness	Dp(XTceal3-Plp1)1Gmh/Y	involves: 129S7/SvEvBrd * C57BL/6	N	23864668
MGI:5529628	M	MP:0001406	abnormal gait	Dp(XTceal3-Plp1)1Gmh/Y	involves: 129S7/SvEvBrd * C57BL/6	N	23864668
MGI:5529628	M	MP:0008503	abnormal spinal cord grey matter morphology	Dp(XTceal3-Plp1)1Gmh/Y	involves: 129S7/SvEvBrd * C57BL/6	N	23864668
MGI:5529628	M	MP:0003631	nervous system phenotype	Dp(XTceal3-Plp1)1Gmh/Y	involves: 129S7/SvEvBrd * C57BL/6	Y	23864668
MGI:5529628	M	MP:0001265	decreased body size	Dp(XTceal3-Plp1)1Gmh/Y	involves: 129S7/SvEvBrd * C57BL/6	N	23864668
MGI:5529628	M	MP:0008025	brain vacuoles	Dp(XTceal3-Plp1)1Gmh/Y	involves: 129S7/SvEvBrd * C57BL/6	N	23864668
MGI:5529628	M	MP:0005405	axon degeneration	Dp(XTceal3-Plp1)1Gmh/Y	involves: 129S7/SvEvBrd * C57BL/6	N	23864668
MGI:5529628	M	MP:0001961	abnormal reflex	Dp(XTceal3-Plp1)1Gmh/Y	involves: 129S7/SvEvBrd * C57BL/6	N	23864668
MGI:5529628	M	MP:0003354	astrocytosis	Dp(XTceal3-Plp1)1Gmh/Y	involves: 129S7/SvEvBrd * C57BL/6	N	23864668
MGI:5529628	M	MP:0000920	abnormal myelination	Dp(XTceal3-Plp1)1Gmh/Y	involves: 129S7/SvEvBrd * C57BL/6	N	23864668
MGI:5529628	M	MP:0000921	demyelination	Dp(XTceal3-Plp1)1Gmh/Y	involves: 129S7/SvEvBrd * C57BL/6	N	23864668
MGI:5532293	F	MP:0005386	behavior/neurological phenotype	Gtf2i<tm1Vcam>/Gtf2i<tm1Vcam>	involves: 129S1/Sv * 129X1/SvJ * CD-1	Y	20403157
MGI:5532293	M	MP:0003205	testicular atrophy	Gtf2i<tm1Vcam>/Gtf2i<tm1Vcam>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	20403157
MGI:5532293	M	MP:0001147	small testis	Gtf2i<tm1Vcam>/Gtf2i<tm1Vcam>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	20403157
MGI:5532293	F	MP:0001923	reduced female fertility	Gtf2i<tm1Vcam>/Gtf2i<tm1Vcam>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	20403157
MGI:5532293	M	MP:0001922	reduced male fertility	Gtf2i<tm1Vcam>/Gtf2i<tm1Vcam>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	20403157
MGI:5532544	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm331a(Ple275-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm331a(Ple275-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532545	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm332(Ple272-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm332(Ple272-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532548	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm333(Ple281-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm333(Ple281-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532549	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm334a(Ple279-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm334a(Ple279-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532550	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm335(Ple277-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm335(Ple277-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532552	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm336a(Ple134-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm336a(Ple134-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532553	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm337a(Ple285-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm337a(Ple285-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532554	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm338a(Ple284-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm338a(Ple284-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532555	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm339a(Ple280-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm339a(Ple280-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532556	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm340(Ple252-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm340(Ple252-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532558	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm341a(Ple273-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm341a(Ple273-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532559	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm342a(Ple282-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm342a(Ple282-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532560	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm343(Ple270-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm343(Ple270-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532561	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm344a(Ple5-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm344a(Ple5-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532565	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm345a(icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm345a(icre/ERT2)Ems>	N	MGI:5529813
MGI:5532566	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm346a(Ple264-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm346a(Ple264-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532567	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm347a(Ple155-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm347a(Ple155-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532568	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm348a(Ple265-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm348a(Ple265-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532569	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm349a(hs671-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm349a(hs671-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532571	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm350a(Ple232-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm350a(Ple232-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532572	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm351a(Ple198-icre/ERT2)Ems>/Y	B6.Cg-Hprt<tm351a(Ple198-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532573	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm352a(Hspa1a-icre/ERT2)Ems>/Y	B6.Cg-Hprt1<tm352a(Hspa1a-icre/ERT2)Ems>	N	MGI:5529813
MGI:5532579	F	MP:0001926	female infertility	Clpp<Gt(IST11134F10)Tigm>/Clpp<Gt(IST11134F10)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532579	F	MP:0002680	decreased corpora lutea number	Clpp<Gt(IST11134F10)Tigm>/Clpp<Gt(IST11134F10)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532579	M	MP:0001147	small testis	Clpp<Gt(IST11134F10)Tigm>/Clpp<Gt(IST11134F10)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532579	F	MP:0013508	increased granulosa cell apoptosis	Clpp<Gt(IST11134F10)Tigm>/Clpp<Gt(IST11134F10)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532579	M	MP:0005159	azoospermia	Clpp<Gt(IST11134F10)Tigm>/Clpp<Gt(IST11134F10)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532579	F	MP:0010182	decreased susceptibility to weight gain	Clpp<Gt(IST11134F10)Tigm>/Clpp<Gt(IST11134F10)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532579	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Clpp<Gt(IST11134F10)Tigm>/Clpp<Gt(IST11134F10)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532579	F	MP:0008868	abnormal granulosa cell morphology	Clpp<Gt(IST11134F10)Tigm>/Clpp<Gt(IST11134F10)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532579	M	MP:0001155	arrest of spermatogenesis	Clpp<Gt(IST11134F10)Tigm>/Clpp<Gt(IST11134F10)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532579	F	MP:0001931	abnormal oogenesis	Clpp<Gt(IST11134F10)Tigm>/Clpp<Gt(IST11134F10)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532579	M	MP:0001925	male infertility	Clpp<Gt(IST11134F10)Tigm>/Clpp<Gt(IST11134F10)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532579	F	MP:0001127	small ovary	Clpp<Gt(IST11134F10)Tigm>/Clpp<Gt(IST11134F10)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532580	M	MP:0001925	male infertility	Clpp<Gt(IST13563G11)Tigm>/Clpp<Gt(IST13563G11)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532580	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Clpp<Gt(IST13563G11)Tigm>/Clpp<Gt(IST13563G11)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532580	F	MP:0010182	decreased susceptibility to weight gain	Clpp<Gt(IST13563G11)Tigm>/Clpp<Gt(IST13563G11)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532580	F	MP:0001127	small ovary	Clpp<Gt(IST13563G11)Tigm>/Clpp<Gt(IST13563G11)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532580	F	MP:0002680	decreased corpora lutea number	Clpp<Gt(IST13563G11)Tigm>/Clpp<Gt(IST13563G11)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532580	M	MP:0001147	small testis	Clpp<Gt(IST13563G11)Tigm>/Clpp<Gt(IST13563G11)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532580	M	MP:0001155	arrest of spermatogenesis	Clpp<Gt(IST13563G11)Tigm>/Clpp<Gt(IST13563G11)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532580	F	MP:0001931	abnormal oogenesis	Clpp<Gt(IST13563G11)Tigm>/Clpp<Gt(IST13563G11)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532580	F	MP:0008868	abnormal granulosa cell morphology	Clpp<Gt(IST13563G11)Tigm>/Clpp<Gt(IST13563G11)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532580	F	MP:0013504	increased embryonic tissue cell apoptosis	Clpp<Gt(IST13563G11)Tigm>/Clpp<Gt(IST13563G11)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532580	M	MP:0005159	azoospermia	Clpp<Gt(IST13563G11)Tigm>/Clpp<Gt(IST13563G11)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532580	F	MP:0001926	female infertility	Clpp<Gt(IST13563G11)Tigm>/Clpp<Gt(IST13563G11)Tigm>	involves: C57BL/6N	N	23851121
MGI:5532734	F	MP:0005389	reproductive system phenotype	Nr6a1<tm1c(EUCOMM)Wtsi>/Nr6a1<tm1c(EUCOMM)Wtsi>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * C57BL/6 * C57BL/6N * SJL	Y	23762465
MGI:5532744	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm2(CMV-tdTomato)Nat>/Y	involves: 129P2/OlaHsd * C57BL/6	N	24411735
MGI:5532745	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm1(CMV-GFP)Nat>/Y	involves: 129P2/OlaHsd * C57BL/6	N	24411735
MGI:5532830	M	MP:0001262	decreased body weight	Sidt2<tm1.1Hzha>/Sidt2<tm1.1Hzha>	involves: 129S6/SvEvTac * C57BL/6J	N	23776622
MGI:5532830	M	MP:0005217	abnormal pancreatic beta cell morphology	Sidt2<tm1.1Hzha>/Sidt2<tm1.1Hzha>	involves: 129S6/SvEvTac * C57BL/6J	N	23776622
MGI:5532830	M	MP:0005293	impaired glucose tolerance	Sidt2<tm1.1Hzha>/Sidt2<tm1.1Hzha>	involves: 129S6/SvEvTac * C57BL/6J	N	23776622
MGI:5532830	M	MP:0003645	increased pancreatic beta cell number	Sidt2<tm1.1Hzha>/Sidt2<tm1.1Hzha>	involves: 129S6/SvEvTac * C57BL/6J	N	23776622
MGI:5532830	M	MP:0002727	decreased circulating insulin level	Sidt2<tm1.1Hzha>/Sidt2<tm1.1Hzha>	involves: 129S6/SvEvTac * C57BL/6J	N	23776622
MGI:5532830	M	MP:0003564	abnormal insulin secretion	Sidt2<tm1.1Hzha>/Sidt2<tm1.1Hzha>	involves: 129S6/SvEvTac * C57BL/6J	N	23776622
MGI:5532830	M	MP:0001265	decreased body size	Sidt2<tm1.1Hzha>/Sidt2<tm1.1Hzha>	involves: 129S6/SvEvTac * C57BL/6J	N	23776622
MGI:5532830	M	MP:0005559	increased circulating glucose level	Sidt2<tm1.1Hzha>/Sidt2<tm1.1Hzha>	involves: 129S6/SvEvTac * C57BL/6J	N	23776622
MGI:5532835	M	MP:0002764	short tibia	Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Col2a1-cre)1Bhr/0	involves: C57BL/6 * SJL	N	23776632
MGI:5532835	M	MP:0003109	short femur	Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Col2a1-cre)1Bhr/0	involves: C57BL/6 * SJL	N	23776632
MGI:5532835	M	MP:0006396	decreased long bone epiphyseal plate size	Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Col2a1-cre)1Bhr/0	involves: C57BL/6 * SJL	N	23776632
MGI:5532835	M	MP:0004610	small vertebrae	Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Col2a1-cre)1Bhr/0	involves: C57BL/6 * SJL	N	23776632
MGI:5532835	M	MP:0003409	decreased width of hypertrophic chondrocyte zone	Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Col2a1-cre)1Bhr/0	involves: C57BL/6 * SJL	N	23776632
MGI:5532835	M	MP:0003662	abnormal long bone epiphyseal plate proliferative zone	Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Col2a1-cre)1Bhr/0	involves: C57BL/6 * SJL	N	23776632
MGI:5532835	M	MP:0000160	kyphosis	Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Col2a1-cre)1Bhr/0	involves: C57BL/6 * SJL	N	23776632
MGI:5532837	M	MP:0000160	kyphosis	Ntrk2<tm2Lfp>/Ntrk2<tm2Lfp>,Tg(Col2a1-cre)1Bhr/0	involves: 129 * C57BL/6 * SJL	N	23776632
MGI:5532837	M	MP:0006396	decreased long bone epiphyseal plate size	Ntrk2<tm2Lfp>/Ntrk2<tm2Lfp>,Tg(Col2a1-cre)1Bhr/0	involves: 129 * C57BL/6 * SJL	N	23776632
MGI:5532837	M	MP:0003409	decreased width of hypertrophic chondrocyte zone	Ntrk2<tm2Lfp>/Ntrk2<tm2Lfp>,Tg(Col2a1-cre)1Bhr/0	involves: 129 * C57BL/6 * SJL	N	23776632
MGI:5532837	F	MP:0001262	decreased body weight	Ntrk2<tm2Lfp>/Ntrk2<tm2Lfp>,Tg(Col2a1-cre)1Bhr/0	involves: 129 * C57BL/6 * SJL	N	23776632
MGI:5532837	F	MP:0011086	postnatal lethality, incomplete penetrance	Ntrk2<tm2Lfp>/Ntrk2<tm2Lfp>,Tg(Col2a1-cre)1Bhr/0	involves: 129 * C57BL/6 * SJL	N	23776632
MGI:5532837	F	MP:0001265	decreased body size	Ntrk2<tm2Lfp>/Ntrk2<tm2Lfp>,Tg(Col2a1-cre)1Bhr/0	involves: 129 * C57BL/6 * SJL	N	23776632
MGI:5532837	F	MP:0009703	decreased birth body size	Ntrk2<tm2Lfp>/Ntrk2<tm2Lfp>,Tg(Col2a1-cre)1Bhr/0	involves: 129 * C57BL/6 * SJL	N	23776632
MGI:5532923	M	MP:0005386	behavior/neurological phenotype	Tor1a<tm2Wtd>/Tor1a<+>	B6.129S1-Tor1a<tm2Wtd>	Y	22393392
MGI:5532925	M	MP:0001406	abnormal gait	Tor1a<tm2Wtd>/Tor1a<tm2Wtd>	involves: 129S1/Sv * DBA/2J	N	22393392
MGI:5532925	M	MP:0000745	tremors	Tor1a<tm2Wtd>/Tor1a<tm2Wtd>	involves: 129S1/Sv * DBA/2J	N	22393392
MGI:5532925	M	MP:0001431	abnormal eating behavior	Tor1a<tm2Wtd>/Tor1a<tm2Wtd>	involves: 129S1/Sv * DBA/2J	N	22393392
MGI:5538297	F	MP:0005397	hematopoietic system phenotype	Klf8<Gt(AD0101)Wtsi>/Y	FVB.129P2-Klf8<Gt(AD0101)Wtsi>/Apb	Y	23716600
MGI:5538297	F	MP:0002083	premature death	Klf8<Gt(AD0101)Wtsi>/Y	FVB.129P2-Klf8<Gt(AD0101)Wtsi>/Apb	N	23716600
MGI:5538298	M	MP:0005397	hematopoietic system phenotype	Klf8<Gt(AD0101)Wtsi>/Klf8<Gt(AD0101)Wtsi>	FVB.129P2-Klf8<Gt(AD0101)Wtsi>/Apb	Y	23716600
MGI:5538298	M	MP:0002083	premature death	Klf8<Gt(AD0101)Wtsi>/Klf8<Gt(AD0101)Wtsi>	FVB.129P2-Klf8<Gt(AD0101)Wtsi>/Apb	N	23716600
MGI:5538300	F	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Klf3<tm1Merc>/Klf3<tm1Merc>,Klf8<Gt(AD0101)Wtsi>/Klf8<Gt(AD0101)Wtsi>	involves: 129P2/OlaHsd * FVB/NJ	N	23716600
MGI:5538300	F	MP:0011111	lethality during fetal growth through weaning, complete penetrance	Klf3<tm1Merc>/Klf3<tm1Merc>,Klf8<Gt(AD0101)Wtsi>/Klf8<Gt(AD0101)Wtsi>	involves: 129P2/OlaHsd * FVB/NJ	N	23716600
MGI:5538300	F	MP:0005380	embryo phenotype	Klf3<tm1Merc>/Klf3<tm1Merc>,Klf8<Gt(AD0101)Wtsi>/Klf8<Gt(AD0101)Wtsi>	involves: 129P2/OlaHsd * FVB/NJ	Y	23716600
MGI:5538301	F	MP:0011110	preweaning lethality, incomplete penetrance	Klf3<tm1Merc>/Klf3<tm1Merc>,Klf8<Gt(AD0101)Wtsi>/Klf8<+>	involves: 129P2/OlaHsd * FVB/NJ	N	23716600
MGI:5538302	F	MP:0002083	premature death	Klf8<Gt(AD0101)Wtsi>/Klf8<+>	FVB.129P2-Klf8<Gt(AD0101)Wtsi>/Apb	N	23716600
MGI:5538303	M	MP:0011111	lethality during fetal growth through weaning, complete penetrance	Klf3<tm1Merc>/Klf3<tm1Merc>,Klf8<Gt(AD0101)Wtsi>/Y	involves: 129P2/OlaHsd * FVB/NJ	N	23716600
MGI:5538303	M	MP:0005380	embryo phenotype	Klf3<tm1Merc>/Klf3<tm1Merc>,Klf8<Gt(AD0101)Wtsi>/Y	involves: 129P2/OlaHsd * FVB/NJ	Y	23716600
MGI:5538303	M	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance	Klf3<tm1Merc>/Klf3<tm1Merc>,Klf8<Gt(AD0101)Wtsi>/Y	involves: 129P2/OlaHsd * FVB/NJ	N	23716600
MGI:5538381	M	MP:0002781	increased circulating testosterone level	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538381	M	MP:0002997	enlarged seminal vesicle	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538381	M	MP:0004909	increased seminal vesicle weight	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538381	M	MP:0002773	decreased circulating luteinizing hormone level	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538381	M	MP:0001152	increased Leydig cell number	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538381	M	MP:0004961	increased prostate gland weight	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538381	M	MP:0003378	early sexual maturation	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538381	M	MP:0002790	decreased circulating follicle stimulating hormone level	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538381	M	MP:0004928	increased epididymis weight	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538381	M	MP:0004958	enlarged prostate gland	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538381	M	MP:0005389	reproductive system phenotype	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	Y	23861372
MGI:5538381	M	MP:0013604	abnormal adult Leydig cell differentiation	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538381	M	MP:0011385	abnormal testosterone level	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538381	M	MP:0004852	decreased testis weight	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538381	M	MP:0011533	increased urine major urinary protein level	Lhcgr<tm1.1Pnara>/Lhcgr<+>	involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6J	N	23861372
MGI:5538526	M	MP:0002906	increased susceptibility to pharmacologically induced seizures	Mecp2<tm3Meg>/Y	B6.129-Mecp2<tm3Meg>	N	23770587
MGI:5538526	M	MP:0001405	impaired coordination	Mecp2<tm3Meg>/Y	B6.129-Mecp2<tm3Meg>	N	23770587
MGI:5538526	M	MP:0001513	limb grasping	Mecp2<tm3Meg>/Y	B6.129-Mecp2<tm3Meg>	N	23770587
MGI:5538526	M	MP:0002175	decreased brain weight	Mecp2<tm3Meg>/Y	B6.129-Mecp2<tm3Meg>	N	23770587
MGI:5538534	F	MP:0001926	female infertility	Izumo1r<tm1.1Salb>/Izumo1r<tm1.1Salb>	B6.129P2(Cg)-Izumo1r<tm1.1Salb>	N	MGI:3510987
MGI:5538574	M	MP:0001360	abnormal social investigation	Oprm1<tm1Kff>/Oprm1<tm1Kff>	involves: 129S2/SvPas * C57BL/6J	N	20503133
MGI:5538583	F	MP:0010299	increased mammary gland tumor incidence	Tg(MMTV-Erbb2)NK1Mul/0	FVB/N-Tg(MMTV-Erbb2)NK1Mul	N	11200779
MGI:5538601	M	MP:0001922	reduced male fertility	Tbx3<tm1.1Moon>/Tbx3<+>	involves: 129 * C57BL/6 * SJL	N	22203979
MGI:5538601	F	MP:0001923	reduced female fertility	Tbx3<tm1.1Moon>/Tbx3<+>	involves: 129 * C57BL/6 * SJL	N	22203979
MGI:5538717	M	MP:0001922	reduced male fertility	Slirp<tm1.2Pjle>/Slirp<tm1.2Pjle>	involves: C57BL/6	N	23976951
MGI:5538717	M	MP:0020451	decreased sperm progressive motility	Slirp<tm1.2Pjle>/Slirp<tm1.2Pjle>	involves: C57BL/6	N	23976951
MGI:5538717	M	MP:0005389	reproductive system phenotype	Slirp<tm1.2Pjle>/Slirp<tm1.2Pjle>	involves: C57BL/6	Y	23976951
MGI:5538717	M	MP:0009834	abnormal sperm annulus morphology	Slirp<tm1.2Pjle>/Slirp<tm1.2Pjle>	involves: C57BL/6	N	23976951
MGI:5538717	M	MP:0014465	abnormal sperm mitochondrial morphology	Slirp<tm1.2Pjle>/Slirp<tm1.2Pjle>	involves: C57BL/6	N	23976951
MGI:5538719	F	MP:0001132	absent mature ovarian follicles	Spo11<tm1.1Gvpc>/Spo11<tm1.1Gvpc>	involves: C57BL/6	N	23870400
MGI:5538719	F	MP:0001127	small ovary	Spo11<tm1.1Gvpc>/Spo11<tm1.1Gvpc>	involves: C57BL/6	N	23870400
MGI:5538719	F	MP:0003572	abnormal uterus development	Spo11<tm1.1Gvpc>/Spo11<tm1.1Gvpc>	involves: C57BL/6	N	23870400
MGI:5538721	F	MP:0002682	decreased mature ovarian follicle number	Spo11<tm1.1Gvpc>/Spo11<tm3Rdco>	involves: C57BL/6	N	23870400
MGI:5538721	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Spo11<tm1.1Gvpc>/Spo11<tm3Rdco>	involves: C57BL/6	N	23870400
MGI:5538721	F	MP:0008995	early reproductive senescence	Spo11<tm1.1Gvpc>/Spo11<tm3Rdco>	involves: C57BL/6	N	23870400
MGI:5538721	M	MP:0005159	azoospermia	Spo11<tm1.1Gvpc>/Spo11<tm3Rdco>	involves: C57BL/6	N	23870400
MGI:5538721	M	MP:0001925	male infertility	Spo11<tm1.1Gvpc>/Spo11<tm3Rdco>	involves: C57BL/6	N	23870400
MGI:5538721	F	MP:0001127	small ovary	Spo11<tm1.1Gvpc>/Spo11<tm3Rdco>	involves: C57BL/6	N	23870400
MGI:5538721	M	MP:0001147	small testis	Spo11<tm1.1Gvpc>/Spo11<tm3Rdco>	involves: C57BL/6	N	23870400
MGI:5538721	M	MP:0008261	arrest of male meiosis	Spo11<tm1.1Gvpc>/Spo11<tm3Rdco>	involves: C57BL/6	N	23870400
MGI:5543235	F	MP:0002083	premature death	Ikbkg<tm1.1Dwat>/Ikbkg<tm1.1Dwat>,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23871670
MGI:5543236	M	MP:0000609	abnormal liver physiology	Ikbkg<tm1.1Dwat>/Y,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23871670
MGI:5543236	M	MP:0011110	preweaning lethality, incomplete penetrance	Ikbkg<tm1.1Dwat>/Y,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23871670
MGI:5543236	M	MP:0002083	premature death	Ikbkg<tm1.1Dwat>/Y,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23871670
MGI:5543236	M	MP:0001860	liver inflammation	Ikbkg<tm1.1Dwat>/Y,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23871670
MGI:5543236	M	MP:0000607	abnormal hepatocyte morphology	Ikbkg<tm1.1Dwat>/Y,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23871670
MGI:5543236	M	MP:0005387	immune system phenotype	Ikbkg<tm1.1Dwat>/Y,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	Y	23871670
MGI:5543236	M	MP:0003333	liver fibrosis	Ikbkg<tm1.1Dwat>/Y,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23871670
MGI:5543236	M	MP:0002658	abnormal liver regeneration	Ikbkg<tm1.1Dwat>/Y,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23871670
MGI:5543236	M	MP:0011971	increased circulating lactate dehydrogenase level	Ikbkg<tm1.1Dwat>/Y,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23871670
MGI:5543236	M	MP:0002628	hepatic steatosis	Ikbkg<tm1.1Dwat>/Y,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23871670
MGI:5543236	M	MP:0002941	increased circulating alanine transaminase level	Ikbkg<tm1.1Dwat>/Y,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23871670
MGI:5543236	M	MP:0005344	increased circulating bilirubin level	Ikbkg<tm1.1Dwat>/Y,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23871670
MGI:5543236	M	MP:0005343	increased circulating aspartate transaminase level	Ikbkg<tm1.1Dwat>/Y,Tnfrsf1a<tm1Imx>/Tnfrsf1a<tm1Imx>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	N	23871670
MGI:5543237	F	MP:0003427	parakeratosis	Ikbkg<tm1.1Dwat>/Ikbkg<+>	B6.Cg-Ikbkg<tm1.1Dwat>	N	23871670
MGI:5543237	F	MP:0001242	hyperkeratosis	Ikbkg<tm1.1Dwat>/Ikbkg<+>	B6.Cg-Ikbkg<tm1.1Dwat>	N	23871670
MGI:5543237	F	MP:0005017	decreased B cell number	Ikbkg<tm1.1Dwat>/Ikbkg<+>	B6.Cg-Ikbkg<tm1.1Dwat>	N	23871670
MGI:5543237	F	MP:0001209	spontaneous skin ulceration	Ikbkg<tm1.1Dwat>/Ikbkg<+>	B6.Cg-Ikbkg<tm1.1Dwat>	N	23871670
MGI:5543237	F	MP:0002161	abnormal fertility/fecundity	Ikbkg<tm1.1Dwat>/Ikbkg<+>	B6.Cg-Ikbkg<tm1.1Dwat>	N	23871670
MGI:5543237	F	MP:0000691	enlarged spleen	Ikbkg<tm1.1Dwat>/Ikbkg<+>	B6.Cg-Ikbkg<tm1.1Dwat>	N	23871670
MGI:5543238	M	MP:0011100	preweaning lethality, complete penetrance	Ikbkg<tm1.1Dwat>/Y	B6.Cg-Ikbkg<tm1.1Dwat>	N	23871670
MGI:5543401	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tgfbr2<tm1.2Hlm>/Tgfbr2<tm1.2Hlm>,Tg(Col1a2-cre/ERT,-ALPP)7Cpd/0	involves: 129S6/SvEvTac * C57BL/6 * DBA/2	N	22904682
MGI:5543401	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tgfbr2<tm1.2Hlm>/Tgfbr2<tm1.2Hlm>,Tg(Col1a2-cre/ERT,-ALPP)7Cpd/0	involves: 129S6/SvEvTac * C57BL/6 * DBA/2	N	22904682
MGI:5543600	M	MP:0005669	increased circulating leptin level	Selenom<tm1(KOMP)Vlcg>/Selenom<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	23880772
MGI:5543790	M	MP:0014171	increased fatty acid oxidation	Tbc1d1<Gt(E140H06)Wrst>/Tbc1d1<Gt(E140H06)Wrst>	B6.129P2-Tbc1d1<Gt(E140H06)Wrst>	N	23892475
MGI:5543790	M	MP:0010951	abnormal lipid oxidation	Tbc1d1<Gt(E140H06)Wrst>/Tbc1d1<Gt(E140H06)Wrst>	B6.129P2-Tbc1d1<Gt(E140H06)Wrst>	N	23892475
MGI:5543790	M	MP:0010025	decreased total body fat amount	Tbc1d1<Gt(E140H06)Wrst>/Tbc1d1<Gt(E140H06)Wrst>	B6.129P2-Tbc1d1<Gt(E140H06)Wrst>	N	23892475
MGI:5543790	M	MP:0008965	increased basal metabolism	Tbc1d1<Gt(E140H06)Wrst>/Tbc1d1<Gt(E140H06)Wrst>	B6.129P2-Tbc1d1<Gt(E140H06)Wrst>	N	23892475
MGI:5543790	M	MP:0001764	abnormal homeostasis	Tbc1d1<Gt(E140H06)Wrst>/Tbc1d1<Gt(E140H06)Wrst>	B6.129P2-Tbc1d1<Gt(E140H06)Wrst>	N	23892475
MGI:5543790	M	MP:0005376	homeostasis/metabolism phenotype	Tbc1d1<Gt(E140H06)Wrst>/Tbc1d1<Gt(E140H06)Wrst>	B6.129P2-Tbc1d1<Gt(E140H06)Wrst>	Y	23892475
MGI:5543790	M	MP:0005659	decreased susceptibility to diet-induced obesity	Tbc1d1<Gt(E140H06)Wrst>/Tbc1d1<Gt(E140H06)Wrst>	B6.129P2-Tbc1d1<Gt(E140H06)Wrst>	N	23892475
MGI:5543790	M	MP:0001262	decreased body weight	Tbc1d1<Gt(E140H06)Wrst>/Tbc1d1<Gt(E140H06)Wrst>	B6.129P2-Tbc1d1<Gt(E140H06)Wrst>	N	23892475
MGI:5543790	M	MP:0003961	decreased lean body mass	Tbc1d1<Gt(E140H06)Wrst>/Tbc1d1<Gt(E140H06)Wrst>	B6.129P2-Tbc1d1<Gt(E140H06)Wrst>	N	23892475
MGI:5543790	M	MP:0010379	decreased respiratory quotient	Tbc1d1<Gt(E140H06)Wrst>/Tbc1d1<Gt(E140H06)Wrst>	B6.129P2-Tbc1d1<Gt(E140H06)Wrst>	N	23892475
MGI:5543790	M	MP:0004130	abnormal muscle cell glucose uptake	Tbc1d1<Gt(E140H06)Wrst>/Tbc1d1<Gt(E140H06)Wrst>	B6.129P2-Tbc1d1<Gt(E140H06)Wrst>	N	23892475
MGI:5543907	M	MP:0001272	increased metastatic potential	Braf<tm1Mmcm>/Braf<tm1Mmcm>,Nkx3-1<tm4(cre/ERT2)Mms>/Nkx3-1<+>,Pten<tm1Hwu>/Pten<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	22836754
MGI:5543907	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Braf<tm1Mmcm>/Braf<tm1Mmcm>,Nkx3-1<tm4(cre/ERT2)Mms>/Nkx3-1<+>,Pten<tm1Hwu>/Pten<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	22836754
MGI:5543907	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Braf<tm1Mmcm>/Braf<tm1Mmcm>,Nkx3-1<tm4(cre/ERT2)Mms>/Nkx3-1<+>,Pten<tm1Hwu>/Pten<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	22836754
MGI:5543907	M	MP:0002083	premature death	Braf<tm1Mmcm>/Braf<tm1Mmcm>,Nkx3-1<tm4(cre/ERT2)Mms>/Nkx3-1<+>,Pten<tm1Hwu>/Pten<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	22836754
MGI:5543907	M	MP:0010357	increased prostate gland tumor incidence	Braf<tm1Mmcm>/Braf<tm1Mmcm>,Nkx3-1<tm4(cre/ERT2)Mms>/Nkx3-1<+>,Pten<tm1Hwu>/Pten<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	22836754
MGI:5543910	F	MP:0002016	ovary cyst	Tg(Amh-SMAD2*)#Jebu/0	FVB/N-Tg(Amh-SMAD2*)#Jebu	N	23741457
MGI:5543910	F	MP:0008000	increased ovary tumor incidence	Tg(Amh-SMAD2*)#Jebu/0	FVB/N-Tg(Amh-SMAD2*)#Jebu	N	23741457
MGI:5543910	F	MP:0009442	increased ovarian teratoma incidence	Tg(Amh-SMAD2*)#Jebu/0	FVB/N-Tg(Amh-SMAD2*)#Jebu	N	23741457
MGI:5543911	F	MP:0009442	increased ovarian teratoma incidence	Tg(Amh-SMAD2*)#Jebu/0,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * FVB/N	N	23741457
MGI:5543911	F	MP:0002016	ovary cyst	Tg(Amh-SMAD2*)#Jebu/0,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * FVB/N	N	23741457
MGI:5544015	F	MP:0001577	anemia	Ap4e1<tm1a(KOMP)Wtsi>/Ap4e1<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	23870131
MGI:5544016	F	MP:0010053	decreased grip strength	Dnase1l2<tm1(KOMP)Wtsi>/Dnase1l2<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	23870131
MGI:5544017	F	MP:0001260	increased body weight	Kptn<tm1a(EUCOMM)Wtsi>/Kptn<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	23870131
MGI:5544021	M	MP:0010092	increased circulating magnesium level	Trmt10a<tm1a(EUCOMM)Wtsi>/Trmt10a<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	23870131
MGI:5544024	M	MP:0001732	postnatal growth retardation	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6N	N	23870131
MGI:5544024	M	MP:0000162	lordosis	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6N	N	23870131
MGI:5544024	M	MP:0000747	muscle weakness	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6N	N	23870131
MGI:5544024	M	MP:0001925	male infertility	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6N	N	23870131
MGI:5544024	M	MP:0003961	decreased lean body mass	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6N	N	23870131
MGI:5544024	M	MP:0000063	decreased bone mineral density	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6N	N	23870131
MGI:5544027	F	MP:0003961	decreased lean body mass	Crlf3<tm1a(KOMP)Wtsi>/Crlf3<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	23870131
MGI:5544028	F	MP:0003961	decreased lean body mass	Atp5f1a<tm1a(EUCOMM)Wtsi>/Atp5f1a<+>	involves: C57BL/6N	N	23870131
MGI:5544071	M	MP:0008995	early reproductive senescence	Jmjd1c<tm1Mtac>/Jmjd1c<tm1Mtac>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	24006281
MGI:5544071	M	MP:0001147	small testis	Jmjd1c<tm1Mtac>/Jmjd1c<tm1Mtac>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	24006281
MGI:5544071	M	MP:0002687	oligozoospermia	Jmjd1c<tm1Mtac>/Jmjd1c<tm1Mtac>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	24006281
MGI:5544071	M	MP:0004852	decreased testis weight	Jmjd1c<tm1Mtac>/Jmjd1c<tm1Mtac>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	24006281
MGI:5544071	F	MP:0005389	reproductive system phenotype	Jmjd1c<tm1Mtac>/Jmjd1c<tm1Mtac>	involves: C57BL/6NCrlj * CBA/JNCrlj	Y	24006281
MGI:5544071	M	MP:0006378	abnormal spermatogonia morphology	Jmjd1c<tm1Mtac>/Jmjd1c<tm1Mtac>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	24006281
MGI:5544071	M	MP:0014052	increased male germ cell apoptosis	Jmjd1c<tm1Mtac>/Jmjd1c<tm1Mtac>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	24006281
MGI:5544071	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Jmjd1c<tm1Mtac>/Jmjd1c<tm1Mtac>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	24006281
MGI:5544071	M	MP:0001154	seminiferous tubule degeneration	Jmjd1c<tm1Mtac>/Jmjd1c<tm1Mtac>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	24006281
MGI:5544071	M	MP:0004901	decreased male germ cell number	Jmjd1c<tm1Mtac>/Jmjd1c<tm1Mtac>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	24006281
MGI:5544078	M	MP:0008544	impaired olfaction	Tg(Snca-SNCA/GFP)#Jyl/Tg(Snca-SNCA/GFP)#Jyl	involves: C57BL/6	N	23643841
MGI:5544078	M	MP:0003462	abnormal response to novel odor	Tg(Snca-SNCA/GFP)#Jyl/Tg(Snca-SNCA/GFP)#Jyl	involves: C57BL/6	N	23643841
MGI:5544078	F	MP:0001402	decreased locomotor activity	Tg(Snca-SNCA/GFP)#Jyl/Tg(Snca-SNCA/GFP)#Jyl	involves: C57BL/6	N	23643841
MGI:5544078	F	MP:0001405	impaired coordination	Tg(Snca-SNCA/GFP)#Jyl/Tg(Snca-SNCA/GFP)#Jyl	involves: C57BL/6	N	23643841
MGI:5544197	M	MP:0002882	abnormal neuron morphology	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai/0	C57BL/6-Tg(Thy1-VAPB*P56S,-EGFP)D3Cai	N	23771029
MGI:5544197	M	MP:0002878	abnormal corticospinal tract morphology	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai/0	C57BL/6-Tg(Thy1-VAPB*P56S,-EGFP)D3Cai	N	23771029
MGI:5544197	M	MP:0031391	increased locomotor activity	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai/0	C57BL/6-Tg(Thy1-VAPB*P56S,-EGFP)D3Cai	N	23771029
MGI:5544197	M	MP:0001407	short stride length	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai/0	C57BL/6-Tg(Thy1-VAPB*P56S,-EGFP)D3Cai	N	23771029
MGI:5544197	M	MP:0000939	decreased motor neuron number	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai/0	C57BL/6-Tg(Thy1-VAPB*P56S,-EGFP)D3Cai	N	23771029
MGI:5544197	M	MP:0003633	abnormal nervous system physiology	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai/0	C57BL/6-Tg(Thy1-VAPB*P56S,-EGFP)D3Cai	N	23771029
MGI:5544197	M	MP:0001262	decreased body weight	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai/0	C57BL/6-Tg(Thy1-VAPB*P56S,-EGFP)D3Cai	N	23771029
MGI:5544197	M	MP:0008571	abnormal synaptic bouton morphology	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai/0	C57BL/6-Tg(Thy1-VAPB*P56S,-EGFP)D3Cai	N	23771029
MGI:5544197	M	MP:0002574	increased vertical activity	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai/0	C57BL/6-Tg(Thy1-VAPB*P56S,-EGFP)D3Cai	N	23771029
MGI:5544197	M	MP:0000938	motor neuron degeneration	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai/0	C57BL/6-Tg(Thy1-VAPB*P56S,-EGFP)D3Cai	N	23771029
MGI:5544197	M	MP:0001405	impaired coordination	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai/0	C57BL/6-Tg(Thy1-VAPB*P56S,-EGFP)D3Cai	N	23771029
MGI:5544201	F	MP:0002016	ovary cyst	Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * FVB/N	N	23741457
MGI:5544201	F	MP:0013236	ovary degeneration	Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * FVB/N	N	23741457
MGI:5544308	M	MP:0003267	constipation	Snca<tm1Rosl>/Snca<tm1Rosl>,Tg(SNCA)OVX37Rwm/0	B6.Cg-Tg(SNCA)OVX37Rwm Snca<tm1Rosl>	N	24082145
MGI:5544331	F	MP:0001541	abnormal osteoclast physiology	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0010879	decreased trabecular bone volume	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0000066	osteoporosis	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0004984	increased osteoclast cell number	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0004986	abnormal osteoblast morphology	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0004989	decreased osteoblast cell number	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0004992	increased bone resorption	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0000166	abnormal chondrocyte morphology	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0002113	abnormal skeleton development	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0003172	abnormal lysosome physiology	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0004704	short vertebral column	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0001265	decreased body size	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0011711	impaired osteoblast differentiation	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0003797	abnormal compact bone morphology	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0004016	decreased bone mass	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0004214	abnormal long bone diaphysis morphology	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0008753	abnormal osteocyte morphology	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0005508	abnormal skeleton morphology	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0006395	abnormal epiphyseal plate morphology	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544331	F	MP:0000063	decreased bone mineral density	Gnptab<tm1Kkol>/Gnptab<tm1Kkol>	involves: 129 * C57BL/6	N	24127423
MGI:5544419	F	MP:0005387	immune system phenotype	m1Nish/m1Nish<+>	involves: BALB/c * C57BL/6N	Y	23690476
MGI:5544420	F	MP:0005387	immune system phenotype	m1Nish/m1Nish<+>	involves: C57BL/6N	Y	23690476
MGI:5544421	M	MP:0002831	absent Peyer's patches	X/m1Nish	involves: BALB/c * C57BL/6N	N	23690476
MGI:5544421	M	MP:0008045	decreased NK cell number	X/m1Nish	involves: BALB/c * C57BL/6N	N	23690476
MGI:5544421	M	MP:0008071	absent B cells	X/m1Nish	involves: BALB/c * C57BL/6N	N	23690476
MGI:5544422	M	MP:0008045	decreased NK cell number	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544422	M	MP:0001806	decreased IgM level	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544422	M	MP:0002217	small lymph nodes	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544422	M	MP:0005095	decreased T cell proliferation	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544422	M	MP:0008202	absent B-1 B cells	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544422	M	MP:0002144	abnormal B cell differentiation	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544422	M	MP:0008205	absent B-2 B cells	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544422	M	MP:0005017	decreased B cell number	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544422	M	MP:0004978	decreased B-1 B cell number	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544422	M	MP:0005387	immune system phenotype	X/m1Nish	involves: C57BL/6N	Y	23690476
MGI:5544422	M	MP:0002831	absent Peyer's patches	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544422	M	MP:0008053	abnormal NK cell differentiation	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544422	M	MP:0008071	absent B cells	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544422	M	MP:0001805	decreased IgG level	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544422	M	MP:0008215	decreased immature B cell number	X/m1Nish	involves: C57BL/6N	N	23690476
MGI:5544429	F	MP:0031318	enhanced skeletal muscle regeneration	Capn6<tm1Hiso>/Capn6<tm1Hiso>	B6.Cg-Capn6<tm1Hiso>	N	23935533
MGI:5544429	F	MP:0004136	abnormal tongue muscle morphology	Capn6<tm1Hiso>/Capn6<tm1Hiso>	B6.Cg-Capn6<tm1Hiso>	N	23935533
MGI:5544430	M	MP:0000729	abnormal myogenesis	Capn6<tm1Hiso>/Y	B6.Cg-Capn6<tm1Hiso>	N	23935533
MGI:5544582	F	MP:0010767	abnormal female meiosis I arrest	Spin1<Gt(RRZ449)Byg>/Spin1<Gt(RRZ449)Byg>	B6.129P2-Spin1<Gt(RRZ449)Byg>	N	23894536
MGI:5544582	F	MP:0005389	reproductive system phenotype	Spin1<Gt(RRZ449)Byg>/Spin1<Gt(RRZ449)Byg>	B6.129P2-Spin1<Gt(RRZ449)Byg>	Y	23894536
MGI:5544725	M	MP:0001973	increased thermal nociceptive threshold	Gbx1<tm1Mrh>/Gbx1<tm1Mrh>	involves: 129P2/OlaHsd * C57BL/6J	N	24010020
MGI:5544725	F	MP:0011994	increased nerve conduction velocity	Gbx1<tm1Mrh>/Gbx1<tm1Mrh>	involves: 129P2/OlaHsd * C57BL/6J	N	24010020
MGI:5546228	M	MP:0002169	no abnormal phenotype detected	Il2rg<tm1.1Vlcg>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	23918385
MGI:5546331	M	MP:0021206	abnormal limb muscle morphology	Wfikkn2<tm1.1Sjl>/Wfikkn2<tm1.1Sjl>	involves: 129 * C57BL/6	N	24019467
MGI:5546331	M	MP:0010227	decreased quadriceps weight	Wfikkn2<tm1.1Sjl>/Wfikkn2<tm1.1Sjl>	involves: 129 * C57BL/6	N	24019467
MGI:5546331	M	MP:0010239	decreased skeletal muscle weight	Wfikkn2<tm1.1Sjl>/Wfikkn2<tm1.1Sjl>	involves: 129 * C57BL/6	N	24019467
MGI:5546334	M	MP:0021206	abnormal limb muscle morphology	Wfikkn1<tm1.1Sjl>/Wfikkn1<tm1.1Sjl>	involves: 129 * C57BL/6	N	24019467
MGI:5546334	M	MP:0010227	decreased quadriceps weight	Wfikkn1<tm1.1Sjl>/Wfikkn1<tm1.1Sjl>	involves: 129 * C57BL/6	N	24019467
MGI:5546334	M	MP:0010239	decreased skeletal muscle weight	Wfikkn1<tm1.1Sjl>/Wfikkn1<tm1.1Sjl>	involves: 129 * C57BL/6	N	24019467
MGI:5546602	F	MP:0005387	immune system phenotype	Nr4a1<tm1Pcn>/Nr4a1<tm1Pcn>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	21468021
MGI:5547375	F	MP:0004941	abnormal regulatory T cell morphology	Nr4a2<tm1.1Pcn>/Nr4a2<+>,Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>	involves: 129S1/Sv * 129X1/SvJ	N	21468021
MGI:5547376	F	MP:0004941	abnormal regulatory T cell morphology	Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>,Nr4a2<tm1.1Pcn>/Nr4a2<tm1.1Pcn>	involves: 129S1/Sv * 129X1/SvJ	N	21468021
MGI:5547376	F	MP:0004946	abnormal regulatory T cell physiology	Foxp3<tm4(YFP/icre)Ayr>/Foxp3<+>,Nr4a2<tm1.1Pcn>/Nr4a2<tm1.1Pcn>	involves: 129S1/Sv * 129X1/SvJ	N	21468021
MGI:5547618	F	MP:0003725	increased autoantibody level	Tg(CKMM-tTA)A3Rhvh/0,Tg(tetO-H2-K1)#Papl/0	B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	N	10922072
MGI:5547618	F	MP:0004174	abnormal spine curvature	Tg(CKMM-tTA)A3Rhvh/0,Tg(tetO-H2-K1)#Papl/0	B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	N	10922072
MGI:5547618	F	MP:0010090	increased circulating creatine kinase level	Tg(CKMM-tTA)A3Rhvh/0,Tg(tetO-H2-K1)#Papl/0	B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	N	10922072
MGI:5547618	F	MP:0000747	muscle weakness	Tg(CKMM-tTA)A3Rhvh/0,Tg(tetO-H2-K1)#Papl/0	B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	N	10922072
MGI:5547618	F	MP:0001570	abnormal circulating enzyme level	Tg(CKMM-tTA)A3Rhvh/0,Tg(tetO-H2-K1)#Papl/0	B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	N	10922072
MGI:5547618	F	MP:0004794	increased anti-nuclear antigen antibody level	Tg(CKMM-tTA)A3Rhvh/0,Tg(tetO-H2-K1)#Papl/0	B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	N	10922072
MGI:5547618	F	MP:0001402	decreased locomotor activity	Tg(CKMM-tTA)A3Rhvh/0,Tg(tetO-H2-K1)#Papl/0	B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	N	10922072
MGI:5547618	F	MP:0008713	abnormal cytokine level	Tg(CKMM-tTA)A3Rhvh/0,Tg(tetO-H2-K1)#Papl/0	B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	N	10922072
MGI:5547618	F	MP:0001262	decreased body weight	Tg(CKMM-tTA)A3Rhvh/0,Tg(tetO-H2-K1)#Papl/0	B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	N	10922072
MGI:5547618	F	MP:0000759	abnormal skeletal muscle morphology	Tg(CKMM-tTA)A3Rhvh/0,Tg(tetO-H2-K1)#Papl/0	B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	N	10922072
MGI:5547618	F	MP:0009413	skeletal muscle fiber atrophy	Tg(CKMM-tTA)A3Rhvh/0,Tg(tetO-H2-K1)#Papl/0	B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	N	10922072
MGI:5547618	F	MP:0009412	skeletal muscle fiber degeneration	Tg(CKMM-tTA)A3Rhvh/0,Tg(tetO-H2-K1)#Papl/0	B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	N	10922072
MGI:5547618	F	MP:0005150	cachexia	Tg(CKMM-tTA)A3Rhvh/0,Tg(tetO-H2-K1)#Papl/0	B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	N	10922072
MGI:5548175	M	MP:0001260	increased body weight	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0005553	increased circulating creatinine level	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0003982	increased cholesterol level	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0002871	albuminuria	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0001559	hyperglycemia	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0001759	increased urine glucose level	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0001762	polyuria	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0002135	abnormal kidney morphology	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0011941	increased fluid intake	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0001556	increased circulating HDL cholesterol level	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0011939	increased food intake	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0005264	glomerulosclerosis	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0002981	increased liver weight	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0003917	increased kidney weight	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5548175	M	MP:0002833	increased heart weight	Gdf15<tm1Sjl>/Gdf15<tm1Sjl>,Lepr<db>/Lepr<db>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BLKS/J	N	23986522
MGI:5549970	M	MP:0005578	teratozoospermia	Atat1<tm1.2Phep>/Atat1<tm1.2Phep>	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6J	N	23748901
MGI:5549970	M	MP:0009239	short sperm flagellum	Atat1<tm1.2Phep>/Atat1<tm1.2Phep>	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6J	N	23748901
MGI:5549970	M	MP:0001935	decreased litter size	Atat1<tm1.2Phep>/Atat1<tm1.2Phep>	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6J	N	23748901
MGI:5549970	M	MP:0001922	reduced male fertility	Atat1<tm1.2Phep>/Atat1<tm1.2Phep>	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6J	N	23748901
MGI:5549970	M	MP:0004852	decreased testis weight	Atat1<tm1.2Phep>/Atat1<tm1.2Phep>	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6J	N	23748901
MGI:5549970	M	MP:0002675	asthenozoospermia	Atat1<tm1.2Phep>/Atat1<tm1.2Phep>	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6J	N	23748901
MGI:5549970	M	MP:0009834	abnormal sperm annulus morphology	Atat1<tm1.2Phep>/Atat1<tm1.2Phep>	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6J	N	23748901
MGI:5549970	M	MP:0004929	decreased epididymis weight	Atat1<tm1.2Phep>/Atat1<tm1.2Phep>	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6J	N	23748901
MGI:5549970	M	MP:0014052	increased male germ cell apoptosis	Atat1<tm1.2Phep>/Atat1<tm1.2Phep>	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6J	N	23748901
MGI:5549970	M	MP:0002687	oligozoospermia	Atat1<tm1.2Phep>/Atat1<tm1.2Phep>	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6J	N	23748901
MGI:5550098	M	MP:0005377	hearing/vestibular/ear phenotype	Marveld2<tm1.1Sria>/Marveld2<tm1.1Sria>,Pou3f4<del-J>/Y	involves: 129X1/SvJ * C3Heb/FeJ * C57BL/6J	Y	23979167
MGI:5550099	F	MP:0005377	hearing/vestibular/ear phenotype	Marveld2<tm1.1Sria>/Marveld2<tm1.1Sria>,Pou3f4<del-J>/Pou3f4<del-J>	involves: 129X1/SvJ * C3Heb/FeJ * C57BL/6J	Y	23979167
MGI:5550143	F	MP:0009425	increased soleus weight	Ghr<tm1c(KOMP)Wtsi>/Ghr<tm1c(KOMP)Wtsi>,Tg(Fabp4-cre)1Rev/0	involves: C57BL/6N	N	23349524
MGI:5550143	F	MP:0008596	increased circulating interleukin-6 level	Ghr<tm1c(KOMP)Wtsi>/Ghr<tm1c(KOMP)Wtsi>,Tg(Fabp4-cre)1Rev/0	involves: C57BL/6N	N	23349524
MGI:5550143	F	MP:0003917	increased kidney weight	Ghr<tm1c(KOMP)Wtsi>/Ghr<tm1c(KOMP)Wtsi>,Tg(Fabp4-cre)1Rev/0	involves: C57BL/6N	N	23349524
MGI:5550143	M	MP:0004953	decreased spleen weight	Ghr<tm1c(KOMP)Wtsi>/Ghr<tm1c(KOMP)Wtsi>,Tg(Fabp4-cre)1Rev/0	involves: C57BL/6N	N	23349524
MGI:5550143	F	MP:0005669	increased circulating leptin level	Ghr<tm1c(KOMP)Wtsi>/Ghr<tm1c(KOMP)Wtsi>,Tg(Fabp4-cre)1Rev/0	involves: C57BL/6N	N	23349524
MGI:5550143	M	MP:0030968	decreased circulating adiponectin level	Ghr<tm1c(KOMP)Wtsi>/Ghr<tm1c(KOMP)Wtsi>,Tg(Fabp4-cre)1Rev/0	involves: C57BL/6N	N	23349524
MGI:5550143	M	MP:0004702	increased circulating insulin-like growth factor I level	Ghr<tm1c(KOMP)Wtsi>/Ghr<tm1c(KOMP)Wtsi>,Tg(Fabp4-cre)1Rev/0	involves: C57BL/6N	N	23349524
MGI:5550143	F	MP:0009285	increased gonadal fat pad weight	Ghr<tm1c(KOMP)Wtsi>/Ghr<tm1c(KOMP)Wtsi>,Tg(Fabp4-cre)1Rev/0	involves: C57BL/6N	N	23349524
MGI:5550148	M	MP:0004852	decreased testis weight	Stub1<tm1Cpat>/Stub1<tm1Cpat>	involves: 129S/SvEv	N	24113144
MGI:5550383	M	MP:0009538	abnormal synapse morphology	Cacna1f<tm1.1Sdie>/Y	involves: C57BL/6	N	24163243
MGI:5550383	M	MP:0003734	abnormal retina inner plexiform layer morphology	Cacna1f<tm1.1Sdie>/Y	involves: C57BL/6	N	24163243
MGI:5550383	M	MP:0002090	abnormal vision	Cacna1f<tm1.1Sdie>/Y	involves: C57BL/6	N	24163243
MGI:5550383	M	MP:0009392	retina gliosis	Cacna1f<tm1.1Sdie>/Y	involves: C57BL/6	N	24163243
MGI:5550383	M	MP:0002001	blindness	Cacna1f<tm1.1Sdie>/Y	involves: C57BL/6	N	24163243
MGI:5550383	M	MP:0006073	abnormal retina bipolar cell morphology	Cacna1f<tm1.1Sdie>/Y	involves: C57BL/6	N	24163243
MGI:5550383	M	MP:0008444	retina cone cell degeneration	Cacna1f<tm1.1Sdie>/Y	involves: C57BL/6	N	24163243
MGI:5550383	M	MP:0001006	abnormal retina cone cell morphology	Cacna1f<tm1.1Sdie>/Y	involves: C57BL/6	N	24163243
MGI:5550383	M	MP:0012035	abnormal b-wave shape	Cacna1f<tm1.1Sdie>/Y	involves: C57BL/6	N	24163243
MGI:5550383	M	MP:0003731	abnormal retina outer nuclear layer morphology	Cacna1f<tm1.1Sdie>/Y	involves: C57BL/6	N	24163243
MGI:5550383	M	MP:0008519	thin retina outer plexiform layer	Cacna1f<tm1.1Sdie>/Y	involves: C57BL/6	N	24163243
MGI:5550383	M	MP:0006068	abnormal retina horizontal cell morphology	Cacna1f<tm1.1Sdie>/Y	involves: C57BL/6	N	24163243
MGI:5550383	M	MP:0003732	abnormal retina outer plexiform layer morphology	Cacna1f<tm1.1Sdie>/Y	involves: C57BL/6	N	24163243
MGI:5550384	F	MP:0002090	abnormal vision	Cacna1f<tm1.1Sdie>/Cacna1f<+>	involves: C57BL/6	N	24163243
MGI:5550384	F	MP:0006073	abnormal retina bipolar cell morphology	Cacna1f<tm1.1Sdie>/Cacna1f<+>	involves: C57BL/6	N	24163243
MGI:5550384	F	MP:0008519	thin retina outer plexiform layer	Cacna1f<tm1.1Sdie>/Cacna1f<+>	involves: C57BL/6	N	24163243
MGI:5550384	F	MP:0006068	abnormal retina horizontal cell morphology	Cacna1f<tm1.1Sdie>/Cacna1f<+>	involves: C57BL/6	N	24163243
MGI:5550384	F	MP:0001325	abnormal retina morphology	Cacna1f<tm1.1Sdie>/Cacna1f<+>	involves: C57BL/6	N	24163243
MGI:5550384	F	MP:0009392	retina gliosis	Cacna1f<tm1.1Sdie>/Cacna1f<+>	involves: C57BL/6	N	24163243
MGI:5550384	F	MP:0012144	decreased b-wave amplitude	Cacna1f<tm1.1Sdie>/Cacna1f<+>	involves: C57BL/6	N	24163243
MGI:5550384	F	MP:0009538	abnormal synapse morphology	Cacna1f<tm1.1Sdie>/Cacna1f<+>	involves: C57BL/6	N	24163243
MGI:5550384	F	MP:0003731	abnormal retina outer nuclear layer morphology	Cacna1f<tm1.1Sdie>/Cacna1f<+>	involves: C57BL/6	N	24163243
MGI:5550384	F	MP:0005253	abnormal eye physiology	Cacna1f<tm1.1Sdie>/Cacna1f<+>	involves: C57BL/6	N	24163243
MGI:5550384	F	MP:0008444	retina cone cell degeneration	Cacna1f<tm1.1Sdie>/Cacna1f<+>	involves: C57BL/6	N	24163243
MGI:5550446	M	MP:0006035	abnormal mitochondrial morphology	X/Tg(ACTA1-STIM1)2Jmol	involves: FVB/N	N	MGI:3606206
MGI:5550446	M	MP:0003851	skeletal muscle interstitial fibrosis	X/Tg(ACTA1-STIM1)2Jmol	involves: FVB/N	N	MGI:3606206
MGI:5550446	M	MP:0011633	abnormal mitochondrial shape	X/Tg(ACTA1-STIM1)2Jmol	involves: FVB/N	N	MGI:3606206
MGI:5550446	M	MP:0009404	centrally nucleated skeletal muscle fibers	X/Tg(ACTA1-STIM1)2Jmol	involves: FVB/N	N	MGI:3606206
MGI:5550446	M	MP:0004231	abnormal calcium ion homeostasis	X/Tg(ACTA1-STIM1)2Jmol	involves: FVB/N	N	MGI:3606206
MGI:5550465	F	MP:0008028	pregnancy-related premature death	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	8875944
MGI:5550465	F	MP:0000947	convulsive seizures	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	8875944
MGI:5550465	F	MP:0005140	decreased cardiac muscle contractility	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	23254193
MGI:5550465	F	MP:0009661	abnormal pregnancy	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	8875944
MGI:5550465	F	MP:0006144	increased systemic arterial systolic blood pressure	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	23254193
MGI:5550465	F	MP:0002962	increased urine protein level	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	8875944
MGI:5550465	F	MP:0005325	abnormal renal glomerulus morphology	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	8875944
MGI:5550465	F	MP:0003141	cardiac fibrosis	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	23254193
MGI:5550465	F	MP:0009661	abnormal pregnancy	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	23254193
MGI:5550465	F	MP:0004256	abnormal maternal decidual layer morphology	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	8875944
MGI:5550465	F	MP:0010633	myocardium hypertrophy	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	8875944
MGI:5550465	F	MP:0001853	heart inflammation	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	23254193
MGI:5550465	F	MP:0002833	increased heart weight	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	23254193
MGI:5550465	F	MP:0001914	hemorrhage	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	8875944
MGI:5550465	F	MP:0008959	abnormal spongiotrophoblast cell morphology	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	8875944
MGI:5550465	F	MP:0001711	abnormal placenta morphology	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	8875944
MGI:5550465	F	MP:0000231	hypertension	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	8875944
MGI:5550465	F	MP:0012008	delayed parturition	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	8875944
MGI:5550465	F	MP:0002836	abnormal chorion morphology	Tg(AGT)2-5Afu/0	involves: C57BL/6	N	8875944
MGI:5550563	M	MP:0006009	abnormal neuronal migration	Glra2<tm1.2Lngu>/Y,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129S4/SvJae * C57BL/6J * FVB/N * MF1	N	23954789
MGI:5550563	M	MP:0004274	abnormal embryonic/fetal subventricular zone morphology	Glra2<tm1.2Lngu>/Y,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129S4/SvJae * C57BL/6J * FVB/N * MF1	N	23954789
MGI:5550564	M	MP:0006009	abnormal neuronal migration	Glra2<tm1.2Lngu>/Glra2<tm1.2Lngu>,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129S4/SvJae * C57BL/6J * FVB/N * MF1	N	23954789
MGI:5550564	M	MP:0004274	abnormal embryonic/fetal subventricular zone morphology	Glra2<tm1.2Lngu>/Glra2<tm1.2Lngu>,Tg(mI56i-cre,EGFP)1Kc/0	involves: 129S4/SvJae * C57BL/6J * FVB/N * MF1	N	23954789
MGI:5551313	F	MP:0008779	abnormal maternal behavior	Kalrn<tm2.1Npl>/Kalrn<tm2.1Npl>	B6.Cg-Kalrn<tm2.1Npl>	N	23116210
MGI:5551313	M	MP:0001732	postnatal growth retardation	Kalrn<tm2.1Npl>/Kalrn<tm2.1Npl>	B6.Cg-Kalrn<tm2.1Npl>	N	23116210
MGI:5551313	F	MP:0001447	abnormal nest building behavior	Kalrn<tm2.1Npl>/Kalrn<tm2.1Npl>	B6.Cg-Kalrn<tm2.1Npl>	N	23116210
MGI:5551313	F	MP:0008028	pregnancy-related premature death	Kalrn<tm2.1Npl>/Kalrn<tm2.1Npl>	B6.Cg-Kalrn<tm2.1Npl>	N	23116210
MGI:5551313	F	MP:0001262	decreased body weight	Kalrn<tm2.1Npl>/Kalrn<tm2.1Npl>	B6.Cg-Kalrn<tm2.1Npl>	N	23116210
MGI:5551313	F	MP:0001265	decreased body size	Kalrn<tm2.1Npl>/Kalrn<tm2.1Npl>	B6.Cg-Kalrn<tm2.1Npl>	N	23116210
MGI:5551313	F	MP:0012010	parturition failure	Kalrn<tm2.1Npl>/Kalrn<tm2.1Npl>	B6.Cg-Kalrn<tm2.1Npl>	N	23116210
MGI:5551313	F	MP:0003838	abnormal milk ejection	Kalrn<tm2.1Npl>/Kalrn<tm2.1Npl>	B6.Cg-Kalrn<tm2.1Npl>	N	23116210
MGI:5551488	M	MP:0001560	abnormal circulating insulin level	Glp1r<tm1.2Stof>/Glp1r<tm1.2Stof>	Not Specified	N	23959939
MGI:5551488	M	MP:0005291	abnormal glucose tolerance	Glp1r<tm1.2Stof>/Glp1r<tm1.2Stof>	Not Specified	N	23959939
MGI:5551488	M	MP:0005293	impaired glucose tolerance	Glp1r<tm1.2Stof>/Glp1r<tm1.2Stof>	Not Specified	N	23959939
MGI:5551619	M	MP:0006378	abnormal spermatogonia morphology	Kdm6b<tm1.1Iwam>/Kdm6b<tm1.2Iwam>,Tg(Stra8-icre)1Reb/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/NJ	N	23967333
MGI:5551619	M	MP:0013475	delayed reproductive senescence	Kdm6b<tm1.1Iwam>/Kdm6b<tm1.2Iwam>,Tg(Stra8-icre)1Reb/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/NJ	N	23967333
MGI:5551619	M	MP:0001148	enlarged testis	Kdm6b<tm1.1Iwam>/Kdm6b<tm1.2Iwam>,Tg(Stra8-icre)1Reb/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/NJ	N	23967333
MGI:5551619	M	MP:0031425	enhanced male fertility	Kdm6b<tm1.1Iwam>/Kdm6b<tm1.2Iwam>,Tg(Stra8-icre)1Reb/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/NJ	N	23967333
MGI:5551987	M	MP:0011110	preweaning lethality, incomplete penetrance	Sbno2<tm1.1Aki>/Sbno2<tm1.1Aki>	involves: 129 * C57BL/6	N	23980096
MGI:5552711	M	MP:0001922	reduced male fertility	Ropn1<Gt(OST21705)Lex>/Ropn1<Gt(OST21705)Lex>	involves: 129S5/SvEvBrd	N	22021175
MGI:5552711	M	MP:0001935	decreased litter size	Ropn1<Gt(OST21705)Lex>/Ropn1<Gt(OST21705)Lex>	involves: 129S5/SvEvBrd	N	22021175
MGI:5552711	M	MP:0002675	asthenozoospermia	Ropn1<Gt(OST21705)Lex>/Ropn1<Gt(OST21705)Lex>	involves: 129S5/SvEvBrd	N	22021175
MGI:5552712	M	MP:0005389	reproductive system phenotype	Ropn1l<Gt(OST20298)Lex>/Ropn1l<Gt(OST20298)Lex>	involves: 129S5/SvEvBrd	Y	22021175
MGI:5552713	M	MP:0001925	male infertility	Ropn1<Gt(OST21705)Lex>/Ropn1<Gt(OST21705)Lex>,Ropn1l<Gt(OST20298)Lex>/Ropn1l<Gt(OST20298)Lex>	involves: 129S5/SvEvBrd	N	22021175
MGI:5552713	M	MP:0020869	immotile sperm	Ropn1<Gt(OST21705)Lex>/Ropn1<Gt(OST21705)Lex>,Ropn1l<Gt(OST20298)Lex>/Ropn1l<Gt(OST20298)Lex>	involves: 129S5/SvEvBrd	N	22021175
MGI:5552983	F	MP:0005630	increased lung weight	Snord50a/Snord50b<tm1.1Soen>/Snord50a/Snord50b<tm1.1Soen>	B6.129P2-Snord50a/Snord50b<tm1.1Soen>	N	23991050
MGI:5552983	M	MP:0002834	decreased heart weight	Snord50a/Snord50b<tm1.1Soen>/Snord50a/Snord50b<tm1.1Soen>	B6.129P2-Snord50a/Snord50b<tm1.1Soen>	N	23991050
MGI:5552983	M	MP:0004852	decreased testis weight	Snord50a/Snord50b<tm1.1Soen>/Snord50a/Snord50b<tm1.1Soen>	B6.129P2-Snord50a/Snord50b<tm1.1Soen>	N	23991050
MGI:5552987	M	MP:0002834	decreased heart weight	Snord50a/Snord50b<tm1.1Soen>/Snord50a/Snord50b<tm1.1Soen>	B6.129P2-Snord50a/Snord50b<tm1.1Soen>	N	23991050
MGI:5552987	M	MP:0004852	decreased testis weight	Snord50a/Snord50b<tm1.1Soen>/Snord50a/Snord50b<tm1.1Soen>	B6.129P2-Snord50a/Snord50b<tm1.1Soen>	N	23991050
MGI:5552987	F	MP:0005630	increased lung weight	Snord50a/Snord50b<tm1.1Soen>/Snord50a/Snord50b<tm1.1Soen>	B6.129P2-Snord50a/Snord50b<tm1.1Soen>	N	23991050
MGI:5553065	M	MP:0001156	abnormal spermatogenesis	Wdr48<Gt(CSD197)Byg>/Wdr48<+>	B6.129P2-Wdr48<Gt(CSD197)Byg>	N	24001775
MGI:5553065	F	MP:0005431	decreased oocyte number	Wdr48<Gt(CSD197)Byg>/Wdr48<+>	B6.129P2-Wdr48<Gt(CSD197)Byg>	N	24001775
MGI:5553065	F	MP:0001923	reduced female fertility	Wdr48<Gt(CSD197)Byg>/Wdr48<+>	B6.129P2-Wdr48<Gt(CSD197)Byg>	N	24001775
MGI:5553065	M	MP:0003205	testicular atrophy	Wdr48<Gt(CSD197)Byg>/Wdr48<+>	B6.129P2-Wdr48<Gt(CSD197)Byg>	N	24001775
MGI:5553065	M	MP:0001922	reduced male fertility	Wdr48<Gt(CSD197)Byg>/Wdr48<+>	B6.129P2-Wdr48<Gt(CSD197)Byg>	N	24001775
MGI:5553065	M	MP:0004901	decreased male germ cell number	Wdr48<Gt(CSD197)Byg>/Wdr48<+>	B6.129P2-Wdr48<Gt(CSD197)Byg>	N	24001775
MGI:5553065	M	MP:0002216	abnormal seminiferous tubule morphology	Wdr48<Gt(CSD197)Byg>/Wdr48<+>	B6.129P2-Wdr48<Gt(CSD197)Byg>	N	24001775
MGI:5553065	M	MP:0001147	small testis	Wdr48<Gt(CSD197)Byg>/Wdr48<+>	B6.129P2-Wdr48<Gt(CSD197)Byg>	N	24001775
MGI:5553105	M	MP:0002574	increased vertical activity	Ccdc7a<Tg(Prnp-Sirt1)10Imai>/?	B6.Cg-Ccdc7a<Tg(Prnp-Sirt1)10Imai>	N	20668205
MGI:5553105	F	MP:0001399	hyperactivity	Ccdc7a<Tg(Prnp-Sirt1)10Imai>/?	B6.Cg-Ccdc7a<Tg(Prnp-Sirt1)10Imai>	N	20668205
MGI:5553173	F	MP:0001132	absent mature ovarian follicles	Helq<Gt(RRF112)Byg>/Helq<+>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553173	F	MP:0001126	abnormal ovary morphology	Helq<Gt(RRF112)Byg>/Helq<+>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553173	F	MP:0002016	ovary cyst	Helq<Gt(RRF112)Byg>/Helq<+>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553173	F	MP:0004833	ovary atrophy	Helq<Gt(RRF112)Byg>/Helq<+>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553173	F	MP:0002682	decreased mature ovarian follicle number	Helq<Gt(RRF112)Byg>/Helq<+>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553173	F	MP:0002404	increased intestinal adenoma incidence	Helq<Gt(RRF112)Byg>/Helq<+>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553173	F	MP:0002041	increased pituitary adenoma incidence	Helq<Gt(RRF112)Byg>/Helq<+>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553173	F	MP:0012437	increased Harderian gland tumor incidence	Helq<Gt(RRF112)Byg>/Helq<+>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553174	M	MP:0003205	testicular atrophy	Helq<Gt(RRF112)Byg>/Helq<Gt(RRF112)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553174	F	MP:0002016	ovary cyst	Helq<Gt(RRF112)Byg>/Helq<Gt(RRF112)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553174	F	MP:0012411	increased granulosa cell tumor incidence	Helq<Gt(RRF112)Byg>/Helq<Gt(RRF112)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553174	F	MP:0008000	increased ovary tumor incidence	Helq<Gt(RRF112)Byg>/Helq<Gt(RRF112)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553174	F	MP:0002041	increased pituitary adenoma incidence	Helq<Gt(RRF112)Byg>/Helq<Gt(RRF112)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553174	M	MP:0001147	small testis	Helq<Gt(RRF112)Byg>/Helq<Gt(RRF112)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553174	M	MP:0006378	abnormal spermatogonia morphology	Helq<Gt(RRF112)Byg>/Helq<Gt(RRF112)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553174	F	MP:0010299	increased mammary gland tumor incidence	Helq<Gt(RRF112)Byg>/Helq<Gt(RRF112)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553174	F	MP:0004833	ovary atrophy	Helq<Gt(RRF112)Byg>/Helq<Gt(RRF112)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24005329
MGI:5553454	M	MP:0001846	increased inflammatory response	Lrig2<tm1.1Hhed>/Lrig2<tm1.1Hhed>	involves: 129 * C57BL/6 * FVB/N	N	24023893
MGI:5554595	M	MP:0004852	decreased testis weight	Ddx4<tm1.1(cre)Dcp>/Ddx4<+>,Rb1<tm3Tyj>/Rb1<tm3Tyj>	involves: 129S4/SvJae * C57BL/6	N	23858447
MGI:5554595	M	MP:0002161	abnormal fertility/fecundity	Ddx4<tm1.1(cre)Dcp>/Ddx4<+>,Rb1<tm3Tyj>/Rb1<tm3Tyj>	involves: 129S4/SvJae * C57BL/6	N	23858447
MGI:5554595	M	MP:0001147	small testis	Ddx4<tm1.1(cre)Dcp>/Ddx4<+>,Rb1<tm3Tyj>/Rb1<tm3Tyj>	involves: 129S4/SvJae * C57BL/6	N	23858447
MGI:5554595	M	MP:0001925	male infertility	Ddx4<tm1.1(cre)Dcp>/Ddx4<+>,Rb1<tm3Tyj>/Rb1<tm3Tyj>	involves: 129S4/SvJae * C57BL/6	N	23858447
MGI:5554595	M	MP:0001156	abnormal spermatogenesis	Ddx4<tm1.1(cre)Dcp>/Ddx4<+>,Rb1<tm3Tyj>/Rb1<tm3Tyj>	involves: 129S4/SvJae * C57BL/6	N	23858447
MGI:5554676	M	MP:0001706	abnormal left-right axis patterning	Zic3<Ka>/Y	involves: BALB/cOlaHsd * C3H/HeH	N	15384171
MGI:5554676	M	MP:0000269	abnormal heart looping	Zic3<Ka>/Y	involves: BALB/cOlaHsd * C3H/HeH	N	15384171
MGI:5554689	M	MP:0003085	abnormal egg cylinder morphology	Zic3<Ka>/Y	B6.C(C3H)-Zic3<Ka>	N	23471918
MGI:5554689	M	MP:0004252	abnormal direction of heart looping	Zic3<Ka>/Y	B6.C(C3H)-Zic3<Ka>	N	23471918
MGI:5554689	M	MP:0003890	abnormal embryonic-extraembryonic boundary morphology	Zic3<Ka>/Y	B6.C(C3H)-Zic3<Ka>	N	23471918
MGI:5555030	F	MP:0000221	decreased leukocyte cell number	Pitpnm1<tm1a(EUCOMM)Wtsi>/Pitpnm1<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	23820044
MGI:5555030	M	MP:0000195	decreased circulating calcium level	Pitpnm1<tm1a(EUCOMM)Wtsi>/Pitpnm1<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	23820044
MGI:5555030	M	MP:0005179	decreased circulating cholesterol level	Pitpnm1<tm1a(EUCOMM)Wtsi>/Pitpnm1<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	23820044
MGI:5556059	M	MP:0010047	axonal spheroids	Plp1<tm1Kan>/Y,Tspan2<tm1Hbw>/Tspan2<tm1Hbw>	B6.Cg-Tspan2<tm1Hbw> Plp1<tm1Kan>	N	24038504
MGI:5556059	M	MP:0001847	brain inflammation	Plp1<tm1Kan>/Y,Tspan2<tm1Hbw>/Tspan2<tm1Hbw>	B6.Cg-Tspan2<tm1Hbw> Plp1<tm1Kan>	N	24038504
MGI:5556059	M	MP:0000921	demyelination	Plp1<tm1Kan>/Y,Tspan2<tm1Hbw>/Tspan2<tm1Hbw>	B6.Cg-Tspan2<tm1Hbw> Plp1<tm1Kan>	N	24038504
MGI:5556059	M	MP:0001262	decreased body weight	Plp1<tm1Kan>/Y,Tspan2<tm1Hbw>/Tspan2<tm1Hbw>	B6.Cg-Tspan2<tm1Hbw> Plp1<tm1Kan>	N	24038504
MGI:5556059	M	MP:0003354	astrocytosis	Plp1<tm1Kan>/Y,Tspan2<tm1Hbw>/Tspan2<tm1Hbw>	B6.Cg-Tspan2<tm1Hbw> Plp1<tm1Kan>	N	24038504
MGI:5556059	M	MP:0005405	axon degeneration	Plp1<tm1Kan>/Y,Tspan2<tm1Hbw>/Tspan2<tm1Hbw>	B6.Cg-Tspan2<tm1Hbw> Plp1<tm1Kan>	N	24038504
MGI:5556059	M	MP:0008918	microgliosis	Plp1<tm1Kan>/Y,Tspan2<tm1Hbw>/Tspan2<tm1Hbw>	B6.Cg-Tspan2<tm1Hbw> Plp1<tm1Kan>	N	24038504
MGI:5556059	M	MP:0000160	kyphosis	Plp1<tm1Kan>/Y,Tspan2<tm1Hbw>/Tspan2<tm1Hbw>	B6.Cg-Tspan2<tm1Hbw> Plp1<tm1Kan>	N	24038504
MGI:5556059	M	MP:0000755	hindlimb paralysis	Plp1<tm1Kan>/Y,Tspan2<tm1Hbw>/Tspan2<tm1Hbw>	B6.Cg-Tspan2<tm1Hbw> Plp1<tm1Kan>	N	24038504
MGI:5556060	M	MP:0000755	hindlimb paralysis	Plp1<tm1Kan>/Y	B6.129-Plp1<tm1Kan>	N	24038504
MGI:5556060	M	MP:0010047	axonal spheroids	Plp1<tm1Kan>/Y	B6.129-Plp1<tm1Kan>	N	24038504
MGI:5556060	M	MP:0000160	kyphosis	Plp1<tm1Kan>/Y	B6.129-Plp1<tm1Kan>	N	24038504
MGI:5556060	M	MP:0005405	axon degeneration	Plp1<tm1Kan>/Y	B6.129-Plp1<tm1Kan>	N	24038504
MGI:5556060	M	MP:0001262	decreased body weight	Plp1<tm1Kan>/Y	B6.129-Plp1<tm1Kan>	N	24038504
MGI:5556060	M	MP:0008918	microgliosis	Plp1<tm1Kan>/Y	B6.129-Plp1<tm1Kan>	N	24038504
MGI:5556060	M	MP:0003354	astrocytosis	Plp1<tm1Kan>/Y	B6.129-Plp1<tm1Kan>	N	24038504
MGI:5556060	M	MP:0000921	demyelination	Plp1<tm1Kan>/Y	B6.129-Plp1<tm1Kan>	N	24038504
MGI:5556062	F	MP:0001262	decreased body weight	Fkrp<tm1Scbr>/Fkrp<tm1Scbr>,Sox1<tm1(cre)Take>/Sox1<+>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	24234655
MGI:5556107	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Gt(ROSA)26Sor<tm2(CAG-Dsred2/EGFP)Luo>/Gt(ROSA)26Sor<tm1(Notch3*)Sfr>,Notch3<tm1.1(cre/ERT2)Sat>/Notch3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	N	24100291
MGI:5556125	M	MP:0002216	abnormal seminiferous tubule morphology	Tdrd12<tm1Yam>/Tdrd12<tm1Yam>	involves: 129S4/SvJae * C57BL/6	N	24067652
MGI:5556125	M	MP:0003205	testicular atrophy	Tdrd12<tm1Yam>/Tdrd12<tm1Yam>	involves: 129S4/SvJae * C57BL/6	N	24067652
MGI:5556125	M	MP:0001153	small seminiferous tubules	Tdrd12<tm1Yam>/Tdrd12<tm1Yam>	involves: 129S4/SvJae * C57BL/6	N	24067652
MGI:5556125	M	MP:0006380	abnormal spermatid morphology	Tdrd12<tm1Yam>/Tdrd12<tm1Yam>	involves: 129S4/SvJae * C57BL/6	N	24067652
MGI:5556125	M	MP:0001925	male infertility	Tdrd12<tm1Yam>/Tdrd12<tm1Yam>	involves: 129S4/SvJae * C57BL/6	N	24067652
MGI:5556125	M	MP:0001155	arrest of spermatogenesis	Tdrd12<tm1Yam>/Tdrd12<tm1Yam>	involves: 129S4/SvJae * C57BL/6	N	24067652
MGI:5556125	M	MP:0005159	azoospermia	Tdrd12<tm1Yam>/Tdrd12<tm1Yam>	involves: 129S4/SvJae * C57BL/6	N	24067652
MGI:5556125	M	MP:0004543	abnormal sperm physiology	Tdrd12<tm1Yam>/Tdrd12<tm1Yam>	involves: 129S4/SvJae * C57BL/6	N	24067652
MGI:5556400	M	MP:0003205	testicular atrophy	Tinf2<tm2.2Tdl>/Tinf2<+>	involves: BALB/cJ * C57BL/6	N	24449270
MGI:5556400	M	MP:0001154	seminiferous tubule degeneration	Tinf2<tm2.2Tdl>/Tinf2<+>	involves: BALB/cJ * C57BL/6	N	24449270
MGI:5558863	F	MP:0001926	female infertility	Kiss1r<tm1.1Aeh>/Kiss1r<tm1.1Aeh>,Tg(Gnrh1-cre)1Dlc/0	involves: C57BL/6 * CBA	N	24051579
MGI:5558863	F	MP:0004856	decreased ovary weight	Kiss1r<tm1.1Aeh>/Kiss1r<tm1.1Aeh>,Tg(Gnrh1-cre)1Dlc/0	involves: C57BL/6 * CBA	N	24051579
MGI:5558863	M	MP:0005159	azoospermia	Kiss1r<tm1.1Aeh>/Kiss1r<tm1.1Aeh>,Tg(Gnrh1-cre)1Dlc/0	involves: C57BL/6 * CBA	N	24051579
MGI:5558863	M	MP:0004852	decreased testis weight	Kiss1r<tm1.1Aeh>/Kiss1r<tm1.1Aeh>,Tg(Gnrh1-cre)1Dlc/0	involves: C57BL/6 * CBA	N	24051579
MGI:5558863	F	MP:0001144	vagina atresia	Kiss1r<tm1.1Aeh>/Kiss1r<tm1.1Aeh>,Tg(Gnrh1-cre)1Dlc/0	involves: C57BL/6 * CBA	N	24051579
MGI:5558863	M	MP:0005132	decreased luteinizing hormone level	Kiss1r<tm1.1Aeh>/Kiss1r<tm1.1Aeh>,Tg(Gnrh1-cre)1Dlc/0	involves: C57BL/6 * CBA	N	24051579
MGI:5558863	M	MP:0001925	male infertility	Kiss1r<tm1.1Aeh>/Kiss1r<tm1.1Aeh>,Tg(Gnrh1-cre)1Dlc/0	involves: C57BL/6 * CBA	N	24051579
MGI:5559031	M	MP:0005159	azoospermia	Memo1<tm1.1Neh>/Memo1<tm1.1Neh>,Tg(CAG-cre/Esr1*)1Lbe/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	N	24056085
MGI:5559182	M	MP:0005367	renal/urinary system phenotype	Hprt1<tm1(tetO-EGFP/Rac1*)Shaw>/Y	involves: 129S4/SvJae * C57BL/6	Y	24061480
MGI:5559183	M	MP:0008140	podocyte foot process effacement	Hprt1<tm1(tetO-EGFP/Rac1*)Shaw>/Y,Tg(NPHS2-rtTA2*M2)1Jbk/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	24061480
MGI:5559183	M	MP:0002962	increased urine protein level	Hprt1<tm1(tetO-EGFP/Rac1*)Shaw>/Y,Tg(NPHS2-rtTA2*M2)1Jbk/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	24061480
MGI:5559184	M	MP:0005367	renal/urinary system phenotype	Hprt1<tm1(tetO-EGFP/Rac1*)Shaw>/Y,Tg(Nphs1-rtTA*3G)8Jhm/0	involves: 129S4/SvJae * C57BL/6	Y	24061480
MGI:5559184	M	MP:0002962	increased urine protein level	Hprt1<tm1(tetO-EGFP/Rac1*)Shaw>/Y,Tg(Nphs1-rtTA*3G)8Jhm/0	involves: 129S4/SvJae * C57BL/6	N	24061480
MGI:5559208	F	MP:0001923	reduced female fertility	Ap3d1<mh-4J>/Ap3d1<mh-4J>	involves: 129P2/OlaHsd * BALB/cByJ * C57BL/6J	N	MGI:5558048
MGI:5559208	M	MP:0001925	male infertility	Ap3d1<mh-4J>/Ap3d1<mh-4J>	involves: 129P2/OlaHsd * BALB/cByJ * C57BL/6J	N	MGI:5558048
MGI:5559211	F	MP:0001376	abnormal mating receptivity	Del(17)5Mom/Del(17)5Mom	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	24719092
MGI:5559211	M	MP:0011678	abnormal vomeronasal sensory neuron physiology	Del(17)5Mom/Del(17)5Mom	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	24719092
MGI:5559211	F	MP:0008779	abnormal maternal behavior	Del(17)5Mom/Del(17)5Mom	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	24719092
MGI:5559215	F	MP:0005431	decreased oocyte number	Meiob<tm1.1Ics>/Meiob<tm1.1Ics>	involves: C57BL/6NTac	N	24068956
MGI:5559215	M	MP:0001147	small testis	Meiob<tm1.1Ics>/Meiob<tm1.1Ics>	involves: C57BL/6NTac	N	24068956
MGI:5559215	F	MP:0001926	female infertility	Meiob<tm1.1Ics>/Meiob<tm1.1Ics>	involves: C57BL/6NTac	N	24068956
MGI:5559215	M	MP:0004852	decreased testis weight	Meiob<tm1.1Ics>/Meiob<tm1.1Ics>	involves: C57BL/6NTac	N	24068956
MGI:5559215	F	MP:0004805	absent oocytes	Meiob<tm1.1Ics>/Meiob<tm1.1Ics>	involves: C57BL/6NTac	N	24068956
MGI:5559215	M	MP:0005159	azoospermia	Meiob<tm1.1Ics>/Meiob<tm1.1Ics>	involves: C57BL/6NTac	N	24068956
MGI:5559215	F	MP:0001127	small ovary	Meiob<tm1.1Ics>/Meiob<tm1.1Ics>	involves: C57BL/6NTac	N	24068956
MGI:5559215	M	MP:0001925	male infertility	Meiob<tm1.1Ics>/Meiob<tm1.1Ics>	involves: C57BL/6NTac	N	24068956
MGI:5559215	M	MP:0014052	increased male germ cell apoptosis	Meiob<tm1.1Ics>/Meiob<tm1.1Ics>	involves: C57BL/6NTac	N	24068956
MGI:5559215	M	MP:0001155	arrest of spermatogenesis	Meiob<tm1.1Ics>/Meiob<tm1.1Ics>	involves: C57BL/6NTac	N	24068956
MGI:5559331	M	MP:0001925	male infertility	Kcnn2<bc-7J>/Kcnn2<bc-7J>	B6.Cg-Kcnn2<bc-7J>/GrsrJ	N	MGI:5559324
MGI:5559463	M	MP:0003402	decreased liver weight	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0005459	decreased percent body fat/body weight	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0002727	decreased circulating insulin level	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0008963	increased carbon dioxide production	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0011940	decreased food intake	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0001783	decreased white adipose tissue amount	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0005292	improved glucose tolerance	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0002644	decreased circulating triglyceride level	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0005289	increased oxygen consumption	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0005378	growth/size/body region phenotype	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	Y	24367518
MGI:5559463	M	MP:0005418	abnormal circulating hormone level	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0002942	decreased circulating alanine transaminase level	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0005668	decreased circulating leptin level	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0001666	abnormal intestinal absorption	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0010378	increased respiratory quotient	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0001258	decreased body length	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0005659	decreased susceptibility to diet-induced obesity	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559463	M	MP:0002891	increased insulin sensitivity	Slc16a1<tm2.1Lupel>/Slc16a1<+>	B6.129P2-Slc16a1<tm2.1Lupel>	N	24367518
MGI:5559510	M	MP:0001925	male infertility	Ppp1cc<tm1Lex>/Ppp1cc<tm1Lex>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEvBrd * FVB/NJ	N	24089200
MGI:5559510	M	MP:0002675	asthenozoospermia	Ppp1cc<tm1Lex>/Ppp1cc<tm1Lex>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEvBrd * FVB/NJ	N	24089200
MGI:5559510	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Ppp1cc<tm1Lex>/Ppp1cc<tm1Lex>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEvBrd * FVB/NJ	N	24089200
MGI:5559510	M	MP:0002687	oligozoospermia	Ppp1cc<tm1Lex>/Ppp1cc<tm1Lex>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEvBrd * FVB/NJ	N	24089200
MGI:5559510	M	MP:0009237	kinked sperm flagellum	Ppp1cc<tm1Lex>/Ppp1cc<tm1Lex>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEvBrd * FVB/NJ	N	24089200
MGI:5559510	M	MP:0005578	teratozoospermia	Ppp1cc<tm1Lex>/Ppp1cc<tm1Lex>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEvBrd * FVB/NJ	N	24089200
MGI:5559510	F	MP:0005389	reproductive system phenotype	Ppp1cc<tm1Lex>/Ppp1cc<tm1Lex>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEvBrd * FVB/NJ	Y	24089200
MGI:5559689	M	MP:0011874	enlarged urinary bladder	Ppp1r12a<tm1Mzhu>/Ppp1r12a<tm1Mzhu>,Tg(Acta2-cre)#Xya/0	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	23499953
MGI:5559689	M	MP:0002083	premature death	Ppp1r12a<tm1Mzhu>/Ppp1r12a<tm1Mzhu>,Tg(Acta2-cre)#Xya/0	involves: 129S6/SvEvTac * C57BL/6 * CBA	N	23499953
MGI:5559723	M	MP:0011085	postnatal lethality, complete penetrance	mgb/mgb	involves: FVB/N	N	31513549
MGI:5559723	M	MP:0003630	abnormal urothelium morphology	mgb/mgb	involves: FVB/N	N	24023768
MGI:5559723	M	MP:0000519	hydronephrosis	mgb/mgb	involves: FVB/N	N	24023768
MGI:5560479	F	MP:0008000	increased ovary tumor incidence	Tg(Cela1-luc,Cela1-TAg)#Nzh/0	involves: FVB/N	N	19622581
MGI:5560898	M	MP:0012318	slow extinction of fear memory	Cdk5r1<tm2.1Lht>/Cdk5r1<tm2.1Lht>	B6.129-Cdk5r1<tm2.1Lht>	N	24725413
MGI:5560978	M	MP:0006379	abnormal spermatocyte morphology	Mpst<tm1Nori>/Mpst<+>,Tg(CAG-cre)13Miya/0	involves: C57BL/6 * C57BL/6JJcl	N	23759691
MGI:5560978	M	MP:0001152	increased Leydig cell number	Mpst<tm1Nori>/Mpst<+>,Tg(CAG-cre)13Miya/0	involves: C57BL/6 * C57BL/6JJcl	N	23759691
MGI:5560978	M	MP:0001940	testis hypoplasia	Mpst<tm1Nori>/Mpst<+>,Tg(CAG-cre)13Miya/0	involves: C57BL/6 * C57BL/6JJcl	N	23759691
MGI:5560978	F	MP:0005389	reproductive system phenotype	Mpst<tm1Nori>/Mpst<+>,Tg(CAG-cre)13Miya/0	involves: C57BL/6 * C57BL/6JJcl	Y	23759691
MGI:5560978	M	MP:0001925	male infertility	Mpst<tm1Nori>/Mpst<+>,Tg(CAG-cre)13Miya/0	involves: C57BL/6 * C57BL/6JJcl	N	23759691
MGI:5560979	M	MP:0001922	reduced male fertility	Mpst<tm1.1Nori>/Mpst<+>	involves: C57BL/6 * C57BL/6JJcl	N	23759691
MGI:5561051	F	MP:0005168	abnormal female meiosis	Stra8<tm1Ysa>/Stra8<tm1Ysa>	involves: C57BL/6NCrlj * CBA/JNCrlj * Jcl:MCH(ICR)	N	24183939
MGI:5561053	M	MP:0003698	abnormal male reproductive system physiology	Nanos2<tm1Ysa>/Nanos2<tm1Ysa>,Stra8<tm1Ysa>/Stra8<tm1Ysa>	involves: 129 * C57BL/6NCrlj * CBA/JNCrlj * Jcl:MCH(ICR)	N	24183939
MGI:5561053	M	MP:0005169	abnormal male meiosis	Nanos2<tm1Ysa>/Nanos2<tm1Ysa>,Stra8<tm1Ysa>/Stra8<tm1Ysa>	involves: 129 * C57BL/6NCrlj * CBA/JNCrlj * Jcl:MCH(ICR)	N	24183939
MGI:5561055	M	MP:0003698	abnormal male reproductive system physiology	Nanos2<tm1Ysa>/Nanos2<tm1Ysa>,Stra8<tm1Ysa>/Stra8<+>	involves: 129 * C57BL/6NCrlj * CBA/JNCrlj * Jcl:MCH(ICR)	N	24183939
MGI:5561055	M	MP:0005169	abnormal male meiosis	Nanos2<tm1Ysa>/Nanos2<tm1Ysa>,Stra8<tm1Ysa>/Stra8<+>	involves: 129 * C57BL/6NCrlj * CBA/JNCrlj * Jcl:MCH(ICR)	N	24183939
MGI:5562425	F	MP:0002875	decreased erythrocyte cell number	Jak2<m1Dlbr>/Jak2<+>	involves: 129S1/SvImJ * C57BL/6J	N	24086539
MGI:5562427	M	MP:0002875	decreased erythrocyte cell number	Jak2<tm1Jni>/Jak2<+>	involves: 129P2/OlaHsd	N	24086539
MGI:5562644	M	MP:0001923	reduced female fertility	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	N	24155305
MGI:5562644	M	MP:0004811	abnormal neuron physiology	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	N	24155305
MGI:5562644	M	MP:0003631	nervous system phenotype	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	Y	24155305
MGI:5562644	M	MP:0005378	growth/size/body region phenotype	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	Y	24155305
MGI:5562644	M	MP:0004231	abnormal calcium ion homeostasis	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	N	24155305
MGI:5562644	M	MP:0001898	abnormal long-term depression	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	N	24155305
MGI:5562644	M	MP:0005391	vision/eye phenotype	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	Y	24155305
MGI:5562644	M	MP:0009936	abnormal dendritic spine morphology	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	N	24155305
MGI:5562644	M	MP:0005386	behavior/neurological phenotype	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	Y	24155305
MGI:5562644	M	MP:0001402	decreased locomotor activity	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	N	24155305
MGI:5562644	M	MP:0009453	enhanced contextual conditioning behavior	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	N	24155305
MGI:5562644	M	MP:0008414	abnormal spatial reference memory	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	N	24155305
MGI:5562644	M	MP:0009940	abnormal hippocampus pyramidal cell morphology	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	N	24155305
MGI:5562644	M	MP:0001363	increased anxiety-related response	Cpeb3<tm1.2Yshu>/Cpeb3<tm1.2Yshu>	involves: 129S4/SvJae * C57BL/6	N	24155305
MGI:5562686	M	MP:0000231	hypertension	Agxt2<tm1Lex>/Agxt2<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	23023372
MGI:5562878	F	MP:0005161	hematuria	Scarf1<tm1Tkms>/Scarf1<tm1Tkms>	involves: C57BL/6	N	23892722
MGI:5562878	F	MP:0011420	pyuria	Scarf1<tm1Tkms>/Scarf1<tm1Tkms>	involves: C57BL/6	N	23892722
MGI:5562929	M	MP:0002675	asthenozoospermia	Del(8Defb1-Defb13)1Jrdo/Del(8Defb1-Defb13)1Jrdo	involves: 129P2/OlaHsd * C57BL/6N	N	24204287
MGI:5562929	M	MP:0001925	male infertility	Del(8Defb1-Defb13)1Jrdo/Del(8Defb1-Defb13)1Jrdo	involves: 129P2/OlaHsd * C57BL/6N	N	24204287
MGI:5562929	M	MP:0004543	abnormal sperm physiology	Del(8Defb1-Defb13)1Jrdo/Del(8Defb1-Defb13)1Jrdo	involves: 129P2/OlaHsd * C57BL/6N	N	24204287
MGI:5562929	M	MP:0013286	abnormal sperm capacitation	Del(8Defb1-Defb13)1Jrdo/Del(8Defb1-Defb13)1Jrdo	involves: 129P2/OlaHsd * C57BL/6N	N	24204287
MGI:5562929	M	MP:0008893	detached sperm flagellum	Del(8Defb1-Defb13)1Jrdo/Del(8Defb1-Defb13)1Jrdo	involves: 129P2/OlaHsd * C57BL/6N	N	24204287
MGI:5562929	M	MP:0005389	reproductive system phenotype	Del(8Defb1-Defb13)1Jrdo/Del(8Defb1-Defb13)1Jrdo	involves: 129P2/OlaHsd * C57BL/6N	Y	24204287
MGI:5562929	M	MP:0013287	abnormal acrosome reaction	Del(8Defb1-Defb13)1Jrdo/Del(8Defb1-Defb13)1Jrdo	involves: 129P2/OlaHsd * C57BL/6N	N	24204287
MGI:5562929	M	MP:0013288	premature acrosome reaction	Del(8Defb1-Defb13)1Jrdo/Del(8Defb1-Defb13)1Jrdo	involves: 129P2/OlaHsd * C57BL/6N	N	24204287
MGI:5562929	M	MP:0004231	abnormal calcium ion homeostasis	Del(8Defb1-Defb13)1Jrdo/Del(8Defb1-Defb13)1Jrdo	involves: 129P2/OlaHsd * C57BL/6N	N	24204287
MGI:5562929	M	MP:0020451	decreased sperm progressive motility	Del(8Defb1-Defb13)1Jrdo/Del(8Defb1-Defb13)1Jrdo	involves: 129P2/OlaHsd * C57BL/6N	N	24204287
MGI:5562929	M	MP:0030978	impaired binding of sperm to zona pellucida	Del(8Defb1-Defb13)1Jrdo/Del(8Defb1-Defb13)1Jrdo	involves: 129P2/OlaHsd * C57BL/6N	N	24204287
MGI:5562929	M	MP:0009838	abnormal sperm axoneme morphology	Del(8Defb1-Defb13)1Jrdo/Del(8Defb1-Defb13)1Jrdo	involves: 129P2/OlaHsd * C57BL/6N	N	24204287
MGI:5562931	M	MP:0005389	reproductive system phenotype	Del(8Defb1-Defb13)1Jrdo/+	involves: 129P2/OlaHsd * C57BL/6N	Y	24204287
MGI:5563203	F	MP:0001516	abnormal motor coordination/balance	Shank3<tm1.1Pfw>/Shank3<tm1.1Pfw>	B6.129S6-Shank3<tm1.1Pfw>	N	24259569
MGI:5563481	M	MP:0001925	male infertility	Bbip1<tm1.1Gne>/Bbip1<tm1.1Gne>	involves: 129 * C57BL/6J * C57BL/6N	N	24316073
MGI:5564786	M	MP:0010024	increased total body fat amount	Prdm16<tm1.1Brsp>/Prdm16<tm1.1Brsp>,Tg(Adipoq-cre)1Evdr/0	involves: 129/Sv * C57BL/6 * FVB/N	N	24439384
MGI:5564786	M	MP:0010934	increased subcutaneous adipose tissue amount	Prdm16<tm1.1Brsp>/Prdm16<tm1.1Brsp>,Tg(Adipoq-cre)1Evdr/0	involves: 129/Sv * C57BL/6 * FVB/N	N	24439384
MGI:5564786	M	MP:0006094	increased fat cell size	Prdm16<tm1.1Brsp>/Prdm16<tm1.1Brsp>,Tg(Adipoq-cre)1Evdr/0	involves: 129/Sv * C57BL/6 * FVB/N	N	24439384
MGI:5564913	M	MP:0008280	abnormal male germ cell apoptosis	Rbm5<sda>/Rbm5<sda>	C57BL/6-Rbm5<sda>/MarpApb	N	MGI:3611487
MGI:5564913	M	MP:0001925	male infertility	Rbm5<sda>/Rbm5<sda>	C57BL/6-Rbm5<sda>/MarpApb	N	MGI:3611487
MGI:5564913	M	MP:0001155	arrest of spermatogenesis	Rbm5<sda>/Rbm5<sda>	C57BL/6-Rbm5<sda>/MarpApb	N	MGI:3611487
MGI:5564913	M	MP:0006380	abnormal spermatid morphology	Rbm5<sda>/Rbm5<sda>	C57BL/6-Rbm5<sda>/MarpApb	N	MGI:3611487
MGI:5564913	M	MP:0005159	azoospermia	Rbm5<sda>/Rbm5<sda>	C57BL/6-Rbm5<sda>/MarpApb	N	MGI:3611487
MGI:5564923	M	MP:0001147	small testis	Etv5<sco>/Etv5<sco>	involves: C57BL/6JAnu * CBA	N	24204802
MGI:5564923	M	MP:0005159	azoospermia	Etv5<sco>/Etv5<sco>	involves: C57BL/6JAnu * CBA	N	24204802
MGI:5564923	M	MP:0004901	decreased male germ cell number	Etv5<sco>/Etv5<sco>	involves: C57BL/6JAnu * CBA	N	24204802
MGI:5564923	M	MP:0004852	decreased testis weight	Etv5<sco>/Etv5<sco>	involves: C57BL/6JAnu * CBA	N	24204802
MGI:5564923	F	MP:0001926	female infertility	Etv5<sco>/Etv5<sco>	involves: C57BL/6JAnu * CBA	N	24204802
MGI:5564923	M	MP:0001925	male infertility	Etv5<sco>/Etv5<sco>	involves: C57BL/6JAnu * CBA	N	24204802
MGI:5564926	M	MP:0005017	decreased B cell number	Btk<m1Anu>/Btk<m1Anu>,X/Yaa	involves: BXSB/MpJ * C57BL/6JAnu * SB/Le	N	MGI:3611487
MGI:5564928	F	MP:0005017	decreased B cell number	Btk<m1Anu>/Btk<m1Anu>	involves: BXSB/MpJ * C57BL/6JAnu * SB/Le	N	MGI:3611487
MGI:5564983	M	MP:0001922	reduced male fertility	Zfp318<m1Anu>/Zfp318<m1Anu>	C57BL/6JAnu-Zfp318<m1Anu>	N	MGI:3611487
MGI:5565088	M	MP:0005389	reproductive system phenotype	Kmt2a<tm1.1Jjdh>/Kmt2a<tm1.1Jjdh>,Kmt2b<tm1Jjdh>/Kmt2b<tm1Jjdh>	involves: 129X1/SvJ	Y	24176642
MGI:5565089	M	MP:0004852	decreased testis weight	Tasp1<tm1.1Jjdh>/Tasp1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565089	M	MP:0001153	small seminiferous tubules	Tasp1<tm1.1Jjdh>/Tasp1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565089	M	MP:0005159	azoospermia	Tasp1<tm1.1Jjdh>/Tasp1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565089	M	MP:0001925	male infertility	Tasp1<tm1.1Jjdh>/Tasp1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565089	M	MP:0006380	abnormal spermatid morphology	Tasp1<tm1.1Jjdh>/Tasp1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565089	F	MP:0005389	reproductive system phenotype	Tasp1<tm1.1Jjdh>/Tasp1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	Y	24176642
MGI:5565089	M	MP:0001154	seminiferous tubule degeneration	Tasp1<tm1.1Jjdh>/Tasp1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565089	M	MP:0014052	increased male germ cell apoptosis	Tasp1<tm1.1Jjdh>/Tasp1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565089	M	MP:0008279	arrest of spermiogenesis	Tasp1<tm1.1Jjdh>/Tasp1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565163	F	MP:0005389	reproductive system phenotype	Gtf2a1<tm1.1Jjdh>/Gtf2a1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	Y	24176642
MGI:5565163	M	MP:0004852	decreased testis weight	Gtf2a1<tm1.1Jjdh>/Gtf2a1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565163	M	MP:0008279	arrest of spermiogenesis	Gtf2a1<tm1.1Jjdh>/Gtf2a1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565163	M	MP:0001925	male infertility	Gtf2a1<tm1.1Jjdh>/Gtf2a1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565163	M	MP:0006380	abnormal spermatid morphology	Gtf2a1<tm1.1Jjdh>/Gtf2a1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565163	M	MP:0014052	increased male germ cell apoptosis	Gtf2a1<tm1.1Jjdh>/Gtf2a1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565163	M	MP:0001146	abnormal testis morphology	Gtf2a1<tm1.1Jjdh>/Gtf2a1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565163	M	MP:0005159	azoospermia	Gtf2a1<tm1.1Jjdh>/Gtf2a1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565163	M	MP:0001153	small seminiferous tubules	Gtf2a1<tm1.1Jjdh>/Gtf2a1<tm1.1Jjdh>	involves: 129X1/SvJ * C57BL/6	N	24176642
MGI:5565367	F	MP:0001883	increased mammary adenocarcinoma incidence	Met<tm4Gvw>/Met<+>	involves: 129 * C57BL/6J * FVB/N	N	19567831
MGI:5565367	F	MP:0004207	increased squamous cell carcinoma incidence	Met<tm4Gvw>/Met<+>	involves: 129 * C57BL/6J * FVB/N	N	19567831
MGI:5565367	F	MP:0012043	increased myoepithelioma incidence	Met<tm4Gvw>/Met<+>	involves: 129 * C57BL/6J * FVB/N	N	19567831
MGI:5565367	F	MP:0002032	increased sarcoma incidence	Met<tm4Gvw>/Met<+>	involves: 129 * C57BL/6J * FVB/N	N	19567831
MGI:5565367	F	MP:0003667	increased hemangiosarcoma incidence	Met<tm4Gvw>/Met<+>	involves: 129 * C57BL/6J * FVB/N	N	19567831
MGI:5565367	F	MP:0010299	increased mammary gland tumor incidence	Met<tm4Gvw>/Met<+>	involves: 129 * C57BL/6J * FVB/N	N	19567831
MGI:5565476	M	MP:0003331	increased hepatocellular carcinoma incidence	Atm<tm1Awb>/Atm<tm1Awb>	A.129S6-Atm<tm1Awb>	N	24709420
MGI:5565602	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0	FVB-Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp	N	18068632
MGI:5565602	M	MP:0010357	increased prostate gland tumor incidence	Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0	FVB-Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp	N	18068632
MGI:5565602	M	MP:0009737	prostate gland cyst	Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0	FVB-Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp	N	18068632
MGI:5565602	M	MP:0002032	increased sarcoma incidence	Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0	FVB-Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp	N	18068632
MGI:5565602	M	MP:0001272	increased metastatic potential	Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0	FVB-Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp	N	18068632
MGI:5565602	M	MP:0000659	prostate gland hyperplasia	Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0	FVB-Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp	N	14678983
MGI:5565602	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0	FVB-Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp	N	14678983
MGI:5565602	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0	FVB-Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp	N	18068632
MGI:5565603	M	MP:0005379	endocrine/exocrine gland phenotype	Tg(Pbsn-Fgfr2/Fkbp1a)#Dmsp/0	FVB-Tg(Pbsn-Fgfr2/Fkbp1a)#Dmsp	Y	14678983
MGI:5565703	M	MP:0011801	urethra obstruction	Tg(Pbsn-FGFR1*K656E)#Wmck/0	involves: FVB	N	14673947
MGI:5565703	M	MP:0003607	abnormal prostate gland physiology	Tg(Pbsn-FGFR1*K656E)#Wmck/0	involves: FVB	N	14673947
MGI:5565703	M	MP:0004958	enlarged prostate gland	Tg(Pbsn-FGFR1*K656E)#Wmck/0	involves: FVB	N	14673947
MGI:5565703	M	MP:0002083	premature death	Tg(Pbsn-FGFR1*K656E)#Wmck/0	involves: FVB	N	14673947
MGI:5565703	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-FGFR1*K656E)#Wmck/0	involves: FVB	N	14673947
MGI:5565703	M	MP:0001922	reduced male fertility	Tg(Pbsn-FGFR1*K656E)#Wmck/0	involves: FVB	N	14673947
MGI:5565703	M	MP:0000659	prostate gland hyperplasia	Tg(Pbsn-FGFR1*K656E)#Wmck/0	involves: FVB	N	14673947
MGI:5565708	M	MP:0001922	reduced male fertility	Tg(Arr2/Pbsn-FGFR1K656E)1Wmck/0	involves: FVB	N	14695195
MGI:5565708	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Arr2/Pbsn-FGFR1K656E)1Wmck/0	involves: FVB	N	14695195
MGI:5566516	M	MP:0002774	small prostate gland	Tg(Pbsn-FGFR2_iiib*)#Ng/0	Not Specified	N	12492503
MGI:5566516	M	MP:0001168	abnormal prostate gland epithelium morphology	Tg(Pbsn-FGFR2_iiib*)#Ng/0	Not Specified	N	12492503
MGI:5566516	M	MP:0009734	abnormal prostate gland duct morphology	Tg(Pbsn-FGFR2_iiib*)#Ng/0	Not Specified	N	12492503
MGI:5566516	M	MP:0001158	abnormal prostate gland morphology	Tg(Pbsn-FGFR2_iiib*)#Ng/0	Not Specified	N	12492503
MGI:5566518	M	MP:0001158	abnormal prostate gland morphology	Tg(Pbsn-FGF7)3293Ng/0	Not Specified	N	12492503
MGI:5566518	M	MP:0001167	prostate gland epithelial hyperplasia	Tg(Pbsn-FGF7)3293Ng/0	Not Specified	N	12492503
MGI:5566518	M	MP:0001168	abnormal prostate gland epithelium morphology	Tg(Pbsn-FGF7)3293Ng/0	Not Specified	N	12492503
MGI:5566518	M	MP:0000659	prostate gland hyperplasia	Tg(Pbsn-FGF7)3293Ng/0	Not Specified	N	12492503
MGI:5566518	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-FGF7)3293Ng/0	Not Specified	N	12492503
MGI:5566518	M	MP:0009734	abnormal prostate gland duct morphology	Tg(Pbsn-FGF7)3293Ng/0	Not Specified	N	12492503
MGI:5566522	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Arr2/Pbsn-FGFR1K656E)1Wmck/0,Tg(Pbsn-FGFR2_iiib*)#Ng/0	involves: FVB	N	14695195
MGI:5566523	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-FGFR1*K656E)#Wmck/0,Tg(Pbsn-FGFR2_iiib*)#Ng/0	involves: FVB	N	14695195
MGI:5566610	M	MP:0002083	premature death	Apc<tm1Tno>/Apc<tm1Tno>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2	N	17363566
MGI:5566610	M	MP:0001167	prostate gland epithelial hyperplasia	Apc<tm1Tno>/Apc<tm1Tno>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2	N	17363566
MGI:5566610	M	MP:0002020	increased tumor incidence	Apc<tm1Tno>/Apc<tm1Tno>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2	N	17363566
MGI:5566610	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Apc<tm1Tno>/Apc<tm1Tno>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2	N	17363566
MGI:5566610	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Apc<tm1Tno>/Apc<tm1Tno>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2	N	17363566
MGI:5566661	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(Pbsn-Tag)12T10Rjm/0	involves: CD-1	N	11280793
MGI:5566661	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-Tag)12T10Rjm/0	involves: CD-1	N	11280793
MGI:5566661	M	MP:0010357	increased prostate gland tumor incidence	Tg(Pbsn-Tag)12T10Rjm/0	involves: CD-1	N	9645768
MGI:5566661	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(Pbsn-Tag)12T10Rjm/0	involves: CD-1	N	9645768
MGI:5566661	M	MP:0001272	increased metastatic potential	Tg(Pbsn-Tag)12T10Rjm/0	involves: CD-1	N	11280793
MGI:5566676	M	MP:0014052	increased male germ cell apoptosis	Terb1<tm1a(KOMP)Mbp>/Terb1<tm1a(KOMP)Mbp>	C57BL/6-Terb1<tm1a(KOMP)Mbp>	N	24413433
MGI:5566676	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Terb1<tm1a(KOMP)Mbp>/Terb1<tm1a(KOMP)Mbp>	C57BL/6-Terb1<tm1a(KOMP)Mbp>	N	24413433
MGI:5566676	F	MP:0004805	absent oocytes	Terb1<tm1a(KOMP)Mbp>/Terb1<tm1a(KOMP)Mbp>	C57BL/6-Terb1<tm1a(KOMP)Mbp>	N	24413433
MGI:5566676	M	MP:0008261	arrest of male meiosis	Terb1<tm1a(KOMP)Mbp>/Terb1<tm1a(KOMP)Mbp>	C57BL/6-Terb1<tm1a(KOMP)Mbp>	N	24413433
MGI:5566676	F	MP:0002777	absent ovarian follicles	Terb1<tm1a(KOMP)Mbp>/Terb1<tm1a(KOMP)Mbp>	C57BL/6-Terb1<tm1a(KOMP)Mbp>	N	24413433
MGI:5566676	F	MP:0001926	female infertility	Terb1<tm1a(KOMP)Mbp>/Terb1<tm1a(KOMP)Mbp>	C57BL/6-Terb1<tm1a(KOMP)Mbp>	N	24413433
MGI:5566676	M	MP:0001925	male infertility	Terb1<tm1a(KOMP)Mbp>/Terb1<tm1a(KOMP)Mbp>	C57BL/6-Terb1<tm1a(KOMP)Mbp>	N	24413433
MGI:5566676	F	MP:0010767	abnormal female meiosis I arrest	Terb1<tm1a(KOMP)Mbp>/Terb1<tm1a(KOMP)Mbp>	C57BL/6-Terb1<tm1a(KOMP)Mbp>	N	24413433
MGI:5566676	M	MP:0005169	abnormal male meiosis	Terb1<tm1a(KOMP)Mbp>/Terb1<tm1a(KOMP)Mbp>	C57BL/6-Terb1<tm1a(KOMP)Mbp>	N	24413433
MGI:5566676	M	MP:0005159	azoospermia	Terb1<tm1a(KOMP)Mbp>/Terb1<tm1a(KOMP)Mbp>	C57BL/6-Terb1<tm1a(KOMP)Mbp>	N	24413433
MGI:5566676	F	MP:0013236	ovary degeneration	Terb1<tm1a(KOMP)Mbp>/Terb1<tm1a(KOMP)Mbp>	C57BL/6-Terb1<tm1a(KOMP)Mbp>	N	24413433
MGI:5566676	F	MP:0005168	abnormal female meiosis	Terb1<tm1a(KOMP)Mbp>/Terb1<tm1a(KOMP)Mbp>	C57BL/6-Terb1<tm1a(KOMP)Mbp>	N	24413433
MGI:5566677	M	MP:0005169	abnormal male meiosis	Rad21l<tm1Amp>/Rad21l<tm1Amp>	B6.Cg-Rad21l<tm1Amp>	N	24413433
MGI:5566678	M	MP:0005169	abnormal male meiosis	Rec8<mei8>/Rec8<mei8>	B6.Cg-Rec8<mei8>	N	24413433
MGI:5566679	M	MP:0030024	abnormal meiotic attachment of telomere to nuclear envelope	Sun1<tm1Mhan>/Sun1<tm1Mhan>	B6.129S6-Sun1<tm1Mhan>	N	24413433
MGI:5566679	M	MP:0005169	abnormal male meiosis	Sun1<tm1Mhan>/Sun1<tm1Mhan>	B6.129S6-Sun1<tm1Mhan>	N	24413433
MGI:5566699	F	MP:0005168	abnormal female meiosis	Dicer1<em1Psv>/Dicer1<em1Psv>	involves: C57BL/6NCrl	N	24209619
MGI:5566699	M	MP:0005389	reproductive system phenotype	Dicer1<em1Psv>/Dicer1<em1Psv>	involves: C57BL/6NCrl	Y	24209619
MGI:5566699	F	MP:0014445	abnormal spindle assembly in female meiosis	Dicer1<em1Psv>/Dicer1<em1Psv>	involves: C57BL/6NCrl	N	24209619
MGI:5566699	F	MP:0001926	female infertility	Dicer1<em1Psv>/Dicer1<em1Psv>	involves: C57BL/6NCrl	N	24209619
MGI:5566700	M	MP:0005389	reproductive system phenotype	Dicer1<em2Psv>/Dicer1<em2Psv>	involves: C57BL/6NCrl	Y	24209619
MGI:5566700	F	MP:0005168	abnormal female meiosis	Dicer1<em2Psv>/Dicer1<em2Psv>	involves: C57BL/6NCrl	N	24209619
MGI:5566700	F	MP:0014445	abnormal spindle assembly in female meiosis	Dicer1<em2Psv>/Dicer1<em2Psv>	involves: C57BL/6NCrl	N	24209619
MGI:5566700	F	MP:0001926	female infertility	Dicer1<em2Psv>/Dicer1<em2Psv>	involves: C57BL/6NCrl	N	24209619
MGI:5566701	F	MP:0005168	abnormal female meiosis	Dicer1<em3Psv>/Dicer1<em3Psv>	involves: C57BL/6NCrl	N	24209619
MGI:5566701	F	MP:0014445	abnormal spindle assembly in female meiosis	Dicer1<em3Psv>/Dicer1<em3Psv>	involves: C57BL/6NCrl	N	24209619
MGI:5566701	F	MP:0001926	female infertility	Dicer1<em3Psv>/Dicer1<em3Psv>	involves: C57BL/6NCrl	N	24209619
MGI:5566701	M	MP:0005389	reproductive system phenotype	Dicer1<em3Psv>/Dicer1<em3Psv>	involves: C57BL/6NCrl	Y	24209619
MGI:5566833	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(Pbsn-MYC)#Tt/?	involves: C57BL/6J	N	22144662
MGI:5566833	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(Pbsn-MYC)#Tt/?	involves: C57BL/6J	N	22144662
MGI:5566833	M	MP:0001158	abnormal prostate gland morphology	Tg(Pbsn-MYC)#Tt/?	involves: C57BL/6J	N	22144662
MGI:5566875	F	MP:0003572	abnormal uterus development	Pgr<tm1.2Mlia>/Pgr<tm1.2Mlia>	involves: 129X1/SvJ	N	24485460
MGI:5566875	F	MP:0009671	abnormal uterus physiology	Pgr<tm1.2Mlia>/Pgr<tm1.2Mlia>	involves: 129X1/SvJ	N	24485460
MGI:5566877	F	MP:0009671	abnormal uterus physiology	Pgr<tm1.1Mlia>/Pgr<tm1.1Mlia>,Tg(Cdh5-cre)7Mlia/0	involves: 129X1/SvJ * FVB/N	N	24485460
MGI:5566877	F	MP:0001619	abnormal vascular permeability	Pgr<tm1.1Mlia>/Pgr<tm1.1Mlia>,Tg(Cdh5-cre)7Mlia/0	involves: 129X1/SvJ * FVB/N	N	24485460
MGI:5566877	F	MP:0001729	impaired embryo implantation	Pgr<tm1.1Mlia>/Pgr<tm1.1Mlia>,Tg(Cdh5-cre)7Mlia/0	involves: 129X1/SvJ * FVB/N	N	24485460
MGI:5566998	F	MP:0001505	hunched posture	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0011556	increased urine beta2-microglobulin level	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0002083	premature death	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0000745	tremors	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0001513	limb grasping	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0002871	albuminuria	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0002703	abnormal renal tubule morphology	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0001392	abnormal locomotor behavior	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0001406	abnormal gait	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0001263	weight loss	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0005565	increased blood urea nitrogen level	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0002988	decreased urine osmolality	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0001304	cataract	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0001762	polyuria	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5566998	F	MP:0003917	increased kidney weight	Gla<tm1Kul>/Gla<tm1Kul>,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0011941	increased fluid intake	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0001392	abnormal locomotor behavior	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0005565	increased blood urea nitrogen level	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0011556	increased urine beta2-microglobulin level	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0003917	increased kidney weight	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0002871	albuminuria	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0002703	abnormal renal tubule morphology	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0002988	decreased urine osmolality	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0001762	polyuria	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0002882	abnormal neuron morphology	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0001513	limb grasping	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0001505	hunched posture	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0002083	premature death	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0000745	tremors	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0001406	abnormal gait	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0005326	abnormal podocyte morphology	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0001263	weight loss	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567000	M	MP:0001304	cataract	Gla<tm1Kul>/Y,Tg(CAG-A4GALT)#Sais/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	N	24094090
MGI:5567003	F	MP:0011940	decreased food intake	Lep<ob>/Lep<ob>,Nfe2l2<tm1Mym>/Nfe2l2<tm1Mym>	B6.Cg-Nfe2l2<tm1Mym> Lep<ob>	N	23238296
MGI:5567826	F	MP:0001559	hyperglycemia	Hprt1<tm1(Ins2-HBEGF)Herr>/Hprt1<tm1(Ins2-HBEGF)Herr>	involves: 129 * C57BL/6	N	20364121
MGI:5567827	M	MP:0001762	polyuria	Hprt1<tm1(Ins2-HBEGF)Herr>/Y	involves: 129 * C57BL/6	N	20364121
MGI:5567827	M	MP:0003059	decreased insulin secretion	Hprt1<tm1(Ins2-HBEGF)Herr>/Y	involves: 129 * C57BL/6	N	20364121
MGI:5567827	M	MP:0003562	abnormal pancreatic beta cell physiology	Hprt1<tm1(Ins2-HBEGF)Herr>/Y	involves: 129 * C57BL/6	N	20364121
MGI:5567827	M	MP:0001559	hyperglycemia	Hprt1<tm1(Ins2-HBEGF)Herr>/Y	involves: 129 * C57BL/6	N	20364121
MGI:5567827	M	MP:0009113	increased pancreatic beta cell mass	Hprt1<tm1(Ins2-HBEGF)Herr>/Y	involves: 129 * C57BL/6	N	20364121
MGI:5567827	M	MP:0003339	decreased pancreatic beta cell number	Hprt1<tm1(Ins2-HBEGF)Herr>/Y	involves: 129 * C57BL/6	N	20364121
MGI:5567827	M	MP:0003058	increased insulin secretion	Hprt1<tm1(Ins2-HBEGF)Herr>/Y	involves: 129 * C57BL/6	N	20364121
MGI:5567827	M	MP:0005215	abnormal pancreatic islet morphology	Hprt1<tm1(Ins2-HBEGF)Herr>/Y	involves: 129 * C57BL/6	N	20364121
MGI:5567827	M	MP:0001263	weight loss	Hprt1<tm1(Ins2-HBEGF)Herr>/Y	involves: 129 * C57BL/6	N	20364121
MGI:5567827	M	MP:0009114	decreased pancreatic beta cell mass	Hprt1<tm1(Ins2-HBEGF)Herr>/Y	involves: 129 * C57BL/6	N	20364121
MGI:5567827	M	MP:0002083	premature death	Hprt1<tm1(Ins2-HBEGF)Herr>/Y	involves: 129 * C57BL/6	N	20364121
MGI:5567827	M	MP:0030971	ketoacidosis	Hprt1<tm1(Ins2-HBEGF)Herr>/Y	involves: 129 * C57BL/6	N	20364121
MGI:5567827	M	MP:0001426	polydipsia	Hprt1<tm1(Ins2-HBEGF)Herr>/Y	involves: 129 * C57BL/6	N	20364121
MGI:5567828	M	MP:0005379	endocrine/exocrine gland phenotype	Gt(ROSA)26Sor<tm1(EYFP)Cos>/Gt(ROSA)26Sor<+>,Hprt1<tm1(Ins2-HBEGF)Herr>/Y,Tg(Ins2-cre/ERT)1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	Y	20364121
MGI:5567828	M	MP:0005215	abnormal pancreatic islet morphology	Gt(ROSA)26Sor<tm1(EYFP)Cos>/Gt(ROSA)26Sor<+>,Hprt1<tm1(Ins2-HBEGF)Herr>/Y,Tg(Ins2-cre/ERT)1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	20364121
MGI:5567829	M	MP:0005379	endocrine/exocrine gland phenotype	Hprt1<tm1(Ins2-HBEGF)Herr>/Y,Tg(Gcg-HBEGF)#Herr/0	involves: 129 * C57BL/6	Y	20364121
MGI:5567830	M	MP:0009179	abnormal pancreatic alpha cell differentiation	Gt(ROSA)26Sor<tm1(EYFP)Cos>/Gt(ROSA)26Sor<+>,Hprt1<tm1(Ins2-HBEGF)Herr>/Y,Tg(Gcg-rtTA)#Herr/0,Tg(tetO-cre)1Jaw/0	involves: 129X1/SvJ * C57BL/6	N	20364121
MGI:5567841	F	MP:0001926	female infertility	Samd4<m1Btlr>/Samd4<m1Btlr>	C57BL/6J-Samd4<m1Btlr>	N	24799716
MGI:5567841	M	MP:0001925	male infertility	Samd4<m1Btlr>/Samd4<m1Btlr>	C57BL/6J-Samd4<m1Btlr>	N	24799716
MGI:5567980	F	MP:0010279	increased gastrointestinal tumor incidence	Apc<Min>/Apc<+>,Mir10a<tm1.1Ahl>/Mir10a<tm1.1Ahl>	B6.Cg-Mir10a<tm1.1Ahl> Apc<min>	N	24204315
MGI:5568119	M	MP:0009289	decreased epididymal fat pad weight	Crbn<tm1Csp>/Crbn<tm1Csp>	B6N.Cg-Crbn<tm1Csp>	N	23349485
MGI:5568214	M	MP:0001409	increased stereotypic behavior	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * 129/SvJ	N	17936729
MGI:5568214	M	MP:0001261	obese	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * 129/SvJ	N	17936729
MGI:5568214	M	MP:0002083	premature death	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * 129/SvJ	N	17936729
MGI:5568214	M	MP:0001513	limb grasping	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * 129/SvJ	N	17936729
MGI:5568214	M	MP:0001259	abnormal body weight	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * 129/SvJ	N	17936729
MGI:5568214	M	MP:0008489	slow postnatal weight gain	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * 129/SvJ	N	17936729
MGI:5568214	M	MP:0001951	abnormal breathing pattern	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * 129/SvJ	N	17936729
MGI:5568214	M	MP:0001402	decreased locomotor activity	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * 129/SvJ	N	17936729
MGI:5568215	F	MP:0002083	premature death	Mecp2<tm1.1Jtc>/Mecp2<tm1.1Jtc>	involves: 129S6/SvEvTac * 129/SvJ	N	17936729
MGI:5568215	F	MP:0001951	abnormal breathing pattern	Mecp2<tm1.1Jtc>/Mecp2<tm1.1Jtc>	involves: 129S6/SvEvTac * 129/SvJ	N	17936729
MGI:5568215	F	MP:0001513	limb grasping	Mecp2<tm1.1Jtc>/Mecp2<tm1.1Jtc>	involves: 129S6/SvEvTac * 129/SvJ	N	17936729
MGI:5568545	M	MP:0003957	abnormal nitric oxide homeostasis	Hprt1<tm4(Tek-IGF1R)Geno>/Y	B6.129P2-Hprt1<tm4(Tek-IGF1R)Geno>	N	22733797
MGI:5568545	M	MP:0004883	abnormal vascular wound healing	Hprt1<tm4(Tek-IGF1R)Geno>/Y	B6.129P2-Hprt1<tm4(Tek-IGF1R)Geno>	N	22733797
MGI:5568545	M	MP:0003544	abnormal vascular endothelial cell migration	Hprt1<tm4(Tek-IGF1R)Geno>/Y	B6.129P2-Hprt1<tm4(Tek-IGF1R)Geno>	N	22733797
MGI:5568545	M	MP:0004003	abnormal vascular endothelial cell physiology	Hprt1<tm4(Tek-IGF1R)Geno>/Y	B6.129P2-Hprt1<tm4(Tek-IGF1R)Geno>	N	22733797
MGI:5568545	M	MP:0003025	increased vasoconstriction	Hprt1<tm4(Tek-IGF1R)Geno>/Y	B6.129P2-Hprt1<tm4(Tek-IGF1R)Geno>	N	22733797
MGI:5568545	M	MP:0005376	homeostasis/metabolism phenotype	Hprt1<tm4(Tek-IGF1R)Geno>/Y	B6.129P2-Hprt1<tm4(Tek-IGF1R)Geno>	Y	22733797
MGI:5568545	M	MP:0005385	cardiovascular system phenotype	Hprt1<tm4(Tek-IGF1R)Geno>/Y	B6.129P2-Hprt1<tm4(Tek-IGF1R)Geno>	Y	22733797
MGI:5568546	M	MP:0004883	abnormal vascular wound healing	Igf1r<tm2Arge>/Igf1r<+>,Tg(Tek-cre)1Ywa/0	B6.Cg-Tg(Tek-cre)1Ywa Igf1r<tm2Arge>	N	22733797
MGI:5568546	M	MP:0004003	abnormal vascular endothelial cell physiology	Igf1r<tm2Arge>/Igf1r<+>,Tg(Tek-cre)1Ywa/0	B6.Cg-Tg(Tek-cre)1Ywa Igf1r<tm2Arge>	N	22733797
MGI:5568605	F	MP:0004031	insulitis	Tnfrsf9<em1Ygch>/Tnfrsf9<em1Ygch>	NOD/ShiLtDvs-Tnfrsf9<em1Ygch>	N	23974926
MGI:5568605	F	MP:0002078	abnormal glucose homeostasis	Tnfrsf9<em1Ygch>/Tnfrsf9<em1Ygch>	NOD/ShiLtDvs-Tnfrsf9<em1Ygch>	N	23974926
MGI:5568605	F	MP:0005387	immune system phenotype	Tnfrsf9<em1Ygch>/Tnfrsf9<em1Ygch>	NOD/ShiLtDvs-Tnfrsf9<em1Ygch>	Y	23974926
MGI:5568605	F	MP:0002444	abnormal T cell physiology	Tnfrsf9<em1Ygch>/Tnfrsf9<em1Ygch>	NOD/ShiLtDvs-Tnfrsf9<em1Ygch>	N	23974926
MGI:5568606	F	MP:0002444	abnormal T cell physiology	Tnfrsf9<em2Ygch>/Tnfrsf9<em2Ygch>	NOD/ShiLtDvs-Tnfrsf9<em2Ygch>	N	23974926
MGI:5568606	F	MP:0005387	immune system phenotype	Tnfrsf9<em2Ygch>/Tnfrsf9<em2Ygch>	NOD/ShiLtDvs-Tnfrsf9<em2Ygch>	Y	23974926
MGI:5568606	F	MP:0002078	abnormal glucose homeostasis	Tnfrsf9<em2Ygch>/Tnfrsf9<em2Ygch>	NOD/ShiLtDvs-Tnfrsf9<em2Ygch>	N	23974926
MGI:5568606	F	MP:0004031	insulitis	Tnfrsf9<em2Ygch>/Tnfrsf9<em2Ygch>	NOD/ShiLtDvs-Tnfrsf9<em2Ygch>	N	23974926
MGI:5568984	F	MP:0004021	abnormal rod electrophysiology	Nyx<nob>/Nyx<+>	involves: BALB/cGr	N	22896717
MGI:5568994	M	MP:0010053	decreased grip strength	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568994	M	MP:0001943	abnormal respiration	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568994	M	MP:0001262	decreased body weight	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568994	M	MP:0014367	impaired long-term object recognition memory	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568994	M	MP:0001402	decreased locomotor activity	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568994	M	MP:0001363	increased anxiety-related response	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568994	M	MP:0000420	ruffled hair	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568994	M	MP:0003459	increased fear-related response	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568994	M	MP:0005202	lethargy	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568994	M	MP:0001405	impaired coordination	Mecp2<tm1.1Jtc>/Y	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568998	F	MP:0003459	increased fear-related response	Mecp2<tm1.1Jtc>/Mecp2<+>	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568998	F	MP:0001262	decreased body weight	Mecp2<tm1.1Jtc>/Mecp2<+>	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568998	F	MP:0014367	impaired long-term object recognition memory	Mecp2<tm1.1Jtc>/Mecp2<+>	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568998	F	MP:0003997	tonic-clonic seizures	Mecp2<tm1.1Jtc>/Mecp2<+>	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568998	F	MP:0001402	decreased locomotor activity	Mecp2<tm1.1Jtc>/Mecp2<+>	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5568998	F	MP:0001405	impaired coordination	Mecp2<tm1.1Jtc>/Mecp2<+>	involves: 129S6/SvEvTac * C57BL/6	N	24283265
MGI:5569266	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm1.1(CAG-DLL1*,-Venus)Gos>/Y	involves: 129P2/OlaHsd * C57BL/6J * CD-1	N	24167636
MGI:5569267	F	MP:0002169	no abnormal phenotype detected	Hprt1<tm1.1(CAG-DLL1*,-Venus)Gos>/Hprt1<tm1.1(CAG-DLL1*,-Venus)Gos>	involves: 129P2/OlaHsd * C57BL/6J * CD-1	N	24167636
MGI:5569268	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm2.1(CAG-DLL1*,-Venus)Gos>/Y	involves: 129P2/OlaHsd * C57BL/6J * CD-1	N	24167636
MGI:5569269	F	MP:0002169	no abnormal phenotype detected	Hprt1<tm2.1(CAG-DLL1*,-Venus)Gos>/Hprt1<tm2.1(CAG-DLL1*,-Venus)Gos>	involves: 129P2/OlaHsd * C57BL/6J * CD-1	N	24167636
MGI:5569270	M	MP:0002169	no abnormal phenotype detected	Hprt1<tm3.1(CAG-DLL1*,-Venus)Gos>/Y	involves: 129P2/OlaHsd * C57BL/6J * CD-1	N	24167636
MGI:5569271	F	MP:0002169	no abnormal phenotype detected	Hprt1<tm3.1(CAG-DLL1*,-Venus)Gos>/Hprt1<tm3.1(CAG-DLL1*,-Venus)Gos>	involves: 129P2/OlaHsd * C57BL/6J * CD-1	N	24167636
MGI:5569298	M	MP:0005389	reproductive system phenotype	Tspo<tm1.1Wbd>/Tspo<tm1.1Wbd>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6	Y	24174323
MGI:5569485	M	MP:0001131	abnormal ovarian follicle morphology	X/Sry<em1Takas>	involves: C57BL/6 * DBA/2	N	24190364
MGI:5569485	M	MP:0009017	prolonged estrus	X/Sry<em1Takas>	involves: C57BL/6 * DBA/2	N	24190364
MGI:5569485	M	MP:0002995	primary sex reversal	X/Sry<em1Takas>	involves: C57BL/6 * DBA/2	N	24190364
MGI:5569485	M	MP:0011129	decreased tertiary ovarian follicle number	X/Sry<em1Takas>	involves: C57BL/6 * DBA/2	N	24190364
MGI:5569485	M	MP:0001926	female infertility	X/Sry<em1Takas>	involves: C57BL/6 * DBA/2	N	24190364
MGI:5569485	M	MP:0005180	abnormal circulating testosterone level	X/Sry<em1Takas>	involves: C57BL/6 * DBA/2	N	24190364
MGI:5569547	M	MP:0020523	decreased susceptibility to induced hypothermia	G0s2<tm1(KOMP)Vlcg>/G0s2<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	24556704
MGI:5569547	M	MP:0009289	decreased epididymal fat pad weight	G0s2<tm1(KOMP)Vlcg>/G0s2<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	24583640
MGI:5569547	M	MP:0008489	slow postnatal weight gain	G0s2<tm1(KOMP)Vlcg>/G0s2<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	24556704
MGI:5569547	M	MP:0001402	decreased locomotor activity	G0s2<tm1(KOMP)Vlcg>/G0s2<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	24556704
MGI:5569547	F	MP:0001882	abnormal lactation	G0s2<tm1(KOMP)Vlcg>/G0s2<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	24556704
MGI:5569547	M	MP:0009133	decreased white fat cell size	G0s2<tm1(KOMP)Vlcg>/G0s2<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	24583640
MGI:5569547	M	MP:0003443	increased circulating glycerol level	G0s2<tm1(KOMP)Vlcg>/G0s2<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	24556704
MGI:5569547	M	MP:0009283	decreased gonadal fat pad weight	G0s2<tm1(KOMP)Vlcg>/G0s2<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	24556704
MGI:5569547	M	MP:0008034	enhanced lipolysis	G0s2<tm1(KOMP)Vlcg>/G0s2<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	24556704
MGI:5569547	M	MP:0005289	increased oxygen consumption	G0s2<tm1(KOMP)Vlcg>/G0s2<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	24556704
MGI:5569623	M	MP:0010768	mortality/aging	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	Y	24177424
MGI:5569623	M	MP:0001260	increased body weight	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569623	M	MP:0005331	insulin resistance	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569623	M	MP:0005289	increased oxygen consumption	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569623	M	MP:0011939	increased food intake	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569623	M	MP:0001399	hyperactivity	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569623	M	MP:0005658	increased susceptibility to diet-induced obesity	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569623	M	MP:0002079	increased circulating insulin level	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569623	M	MP:0005559	increased circulating glucose level	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569623	M	MP:0005376	homeostasis/metabolism phenotype	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	Y	24177424
MGI:5569623	M	MP:0001559	hyperglycemia	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569623	M	MP:0004129	abnormal respiratory quotient	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569623	M	MP:0005378	growth/size/body region phenotype	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	Y	24177424
MGI:5569623	M	MP:0004889	increased energy expenditure	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569623	M	MP:0005290	decreased oxygen consumption	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569623	M	MP:0002712	increased circulating glucagon level	Htr2c<tm2Jke>/Y,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569624	F	MP:0005376	homeostasis/metabolism phenotype	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	Y	24177424
MGI:5569624	F	MP:0005331	insulin resistance	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569624	F	MP:0001260	increased body weight	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569624	F	MP:0011939	increased food intake	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569624	F	MP:0010768	mortality/aging	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	Y	24177424
MGI:5569624	F	MP:0004129	abnormal respiratory quotient	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569624	F	MP:0001559	hyperglycemia	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569624	F	MP:0005289	increased oxygen consumption	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569624	F	MP:0005658	increased susceptibility to diet-induced obesity	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569624	F	MP:0005290	decreased oxygen consumption	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569624	F	MP:0004889	increased energy expenditure	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569624	F	MP:0002079	increased circulating insulin level	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569624	F	MP:0005559	increased circulating glucose level	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569624	F	MP:0005378	growth/size/body region phenotype	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	Y	24177424
MGI:5569624	F	MP:0001399	hyperactivity	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569624	F	MP:0002712	increased circulating glucagon level	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc1-cre)16Lowl/0	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24177424
MGI:5569625	F	MP:0002079	increased circulating insulin level	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	N	24177424
MGI:5569625	F	MP:0001260	increased body weight	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	N	24177424
MGI:5569625	F	MP:0005376	homeostasis/metabolism phenotype	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	Y	24177424
MGI:5569625	F	MP:0002712	increased circulating glucagon level	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	N	24177424
MGI:5569625	F	MP:0005289	increased oxygen consumption	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	N	24177424
MGI:5569625	F	MP:0005559	increased circulating glucose level	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	N	24177424
MGI:5569625	F	MP:0005378	growth/size/body region phenotype	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	Y	24177424
MGI:5569625	F	MP:0011939	increased food intake	Htr2c<tm2Jke>/Htr2c<tm2Jke>,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	N	24177424
MGI:5569626	M	MP:0002079	increased circulating insulin level	Htr2c<tm2Jke>/Y,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	N	24177424
MGI:5569626	M	MP:0011939	increased food intake	Htr2c<tm2Jke>/Y,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	N	24177424
MGI:5569626	M	MP:0001260	increased body weight	Htr2c<tm2Jke>/Y,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	N	24177424
MGI:5569626	M	MP:0005378	growth/size/body region phenotype	Htr2c<tm2Jke>/Y,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	Y	24177424
MGI:5569626	M	MP:0005559	increased circulating glucose level	Htr2c<tm2Jke>/Y,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	N	24177424
MGI:5569626	M	MP:0005376	homeostasis/metabolism phenotype	Htr2c<tm2Jke>/Y,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	Y	24177424
MGI:5569626	M	MP:0002712	increased circulating glucagon level	Htr2c<tm2Jke>/Y,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	N	24177424
MGI:5569626	M	MP:0005289	increased oxygen consumption	Htr2c<tm2Jke>/Y,Tg(Pomc-cre/ERT2)#Jke/0	involves: 129X1/SvJ * C57BL/6J	N	24177424
MGI:5569766	M	MP:0010181	decreased susceptibility to weight loss	Grb10<tm1.1Fliu>/Grb10<tm1.1Fliu>,Tg(Pdx1-cre)6Tuv/0	involves: 129S/SvEv * C57BL/6 * FVB/N	N	22923474
MGI:5569766	M	MP:0003058	increased insulin secretion	Grb10<tm1.1Fliu>/Grb10<tm1.1Fliu>,Tg(Pdx1-cre)6Tuv/0	involves: 129S/SvEv * C57BL/6 * FVB/N	N	22923474
MGI:5569766	M	MP:0002078	abnormal glucose homeostasis	Grb10<tm1.1Fliu>/Grb10<tm1.1Fliu>,Tg(Pdx1-cre)6Tuv/0	involves: 129S/SvEv * C57BL/6 * FVB/N	N	22923474
MGI:5569766	M	MP:0003562	abnormal pancreatic beta cell physiology	Grb10<tm1.1Fliu>/Grb10<tm1.1Fliu>,Tg(Pdx1-cre)6Tuv/0	involves: 129S/SvEv * C57BL/6 * FVB/N	N	22923474
MGI:5569766	M	MP:0011819	increased pancreatic beta cell proliferation	Grb10<tm1.1Fliu>/Grb10<tm1.1Fliu>,Tg(Pdx1-cre)6Tuv/0	involves: 129S/SvEv * C57BL/6 * FVB/N	N	22923474
MGI:5569766	M	MP:0005560	decreased circulating glucose level	Grb10<tm1.1Fliu>/Grb10<tm1.1Fliu>,Tg(Pdx1-cre)6Tuv/0	involves: 129S/SvEv * C57BL/6 * FVB/N	N	22923474
MGI:5569766	M	MP:0009113	increased pancreatic beta cell mass	Grb10<tm1.1Fliu>/Grb10<tm1.1Fliu>,Tg(Pdx1-cre)6Tuv/0	involves: 129S/SvEv * C57BL/6 * FVB/N	N	22923474
MGI:5569766	M	MP:0005292	improved glucose tolerance	Grb10<tm1.1Fliu>/Grb10<tm1.1Fliu>,Tg(Pdx1-cre)6Tuv/0	involves: 129S/SvEv * C57BL/6 * FVB/N	N	22923474
MGI:5569766	M	MP:0009108	increased pancreas weight	Grb10<tm1.1Fliu>/Grb10<tm1.1Fliu>,Tg(Pdx1-cre)6Tuv/0	involves: 129S/SvEv * C57BL/6 * FVB/N	N	22923474
MGI:5569766	M	MP:0005217	abnormal pancreatic beta cell morphology	Grb10<tm1.1Fliu>/Grb10<tm1.1Fliu>,Tg(Pdx1-cre)6Tuv/0	involves: 129S/SvEv * C57BL/6 * FVB/N	N	22923474
MGI:5569766	M	MP:0005376	homeostasis/metabolism phenotype	Grb10<tm1.1Fliu>/Grb10<tm1.1Fliu>,Tg(Pdx1-cre)6Tuv/0	involves: 129S/SvEv * C57BL/6 * FVB/N	Y	22923474
MGI:5569926	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>,Pten<tm1Rps>/Pten<+>	involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J	N	11854455
MGI:5569926	M	MP:0010357	increased prostate gland tumor incidence	Nkx3-1<tm1Mms>/Nkx3-1<tm1Mms>,Pten<tm1Rps>/Pten<+>	involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J	N	11854455
MGI:5569928	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Nkx3-1<tm1Mms>/Nkx3-1<+>,Pten<tm1Rps>/Pten<+>	involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J	N	11854455
MGI:5569928	M	MP:0010357	increased prostate gland tumor incidence	Nkx3-1<tm1Mms>/Nkx3-1<+>,Pten<tm1Rps>/Pten<+>	involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J	N	11854455
MGI:5569932	M	MP:0001168	abnormal prostate gland epithelium morphology	Pten<tm1Rps>/Pten<+>	involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J	N	11854455
MGI:5569932	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Rps>/Pten<+>	involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J	N	11854455
MGI:5570200	M	MP:0013140	excessive vocalization	Ckap5<tm1.1Eba>/Ckap5<tm1.1Eba>,Tg(Camk2a-cre)T29-1Stl/0	involves: 129S4/SvJaeSor * 129S6/SvEvTac * BALB/c * C57BL * C57BL/6J	N	23936366
MGI:5570200	M	MP:0001529	abnormal vocalization	Ckap5<tm1.1Eba>/Ckap5<tm1.1Eba>,Tg(Camk2a-cre)T29-1Stl/0	involves: 129S4/SvJaeSor * 129S6/SvEvTac * BALB/c * C57BL * C57BL/6J	N	23936366
MGI:5571280	M	MP:0005179	decreased circulating cholesterol level	Umod<Urehd1>/Umod<+>	involves: C3HeB/FeJ	N	23748428
MGI:5571280	F	MP:0004151	decreased circulating iron level	Umod<Urehd1>/Umod<+>	involves: C3HeB/FeJ	N	23748428
MGI:5571280	F	MP:0000198	decreased circulating phosphate level	Umod<Urehd1>/Umod<+>	involves: C3HeB/FeJ	N	23748428
MGI:5571287	M	MP:0003215	renal interstitial fibrosis	Umod<Urehd1>/Umod<Urehd1>	involves: C3HeB/FeJ	N	23748428
MGI:5571287	M	MP:0004154	renal tubular necrosis	Umod<Urehd1>/Umod<Urehd1>	involves: C3HeB/FeJ	N	23748428
MGI:5571298	M	MP:0004852	decreased testis weight	Otx2<tm1Pas>/Otx2<+>	involves: C57BL/6 * FVB/N	N	23811236
MGI:5571298	F	MP:0011110	preweaning lethality, incomplete penetrance	Otx2<tm1Pas>/Otx2<+>	involves: C57BL/6 * FVB/N	N	23811236
MGI:5571298	M	MP:0001922	reduced male fertility	Otx2<tm1Pas>/Otx2<+>	involves: C57BL/6 * FVB/N	N	23811236
MGI:5571298	M	MP:0001935	decreased litter size	Otx2<tm1Pas>/Otx2<+>	involves: C57BL/6 * FVB/N	N	23811236
MGI:5571298	M	MP:0002773	decreased circulating luteinizing hormone level	Otx2<tm1Pas>/Otx2<+>	involves: C57BL/6 * FVB/N	N	23811236
MGI:5571298	M	MP:0008325	abnormal gonadotroph morphology	Otx2<tm1Pas>/Otx2<+>	involves: C57BL/6 * FVB/N	N	23811236
MGI:5571298	M	MP:0008335	decreased gonadotroph cell number	Otx2<tm1Pas>/Otx2<+>	involves: C57BL/6 * FVB/N	N	23811236
MGI:5571358	F	MP:0002151	abnormal neural tube morphology	Nap1l2<tm2.1Ucr>/Nap1l2<tm2.1Ucr>,Gt(ROSA)26Sor<tm1Sor>/Gt(ROSA)26Sor<+>	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6	N	MGI:2655403
MGI:5571359	F	MP:0002151	abnormal neural tube morphology	Nap1l2<tm2.1Ucr>/Y,Gt(ROSA)26Sor<tm1Sor>/Gt(ROSA)26Sor<+>	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6	N	MGI:2655403
MGI:5571380	M	MP:0009647	decreased fertilization frequency	Tex101<tm1Qzh>/Tex101<tm1Qzh>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR)	N	23969891
MGI:5571380	M	MP:0001925	male infertility	Tex101<tm1Qzh>/Tex101<tm1Qzh>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR)	N	23969891
MGI:5571380	M	MP:0030978	impaired binding of sperm to zona pellucida	Tex101<tm1Qzh>/Tex101<tm1Qzh>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR)	N	23969891
MGI:5571380	M	MP:0031012	impaired sperm migration in female genital tract	Tex101<tm1Qzh>/Tex101<tm1Qzh>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR)	N	23969891
MGI:5571486	M	MP:0004929	decreased epididymis weight	Ahr<tm1.2Arte>/Ahr<tm1.2Arte>	involves: C57BL/6NTac	N	24174576
MGI:5571486	M	MP:0004852	decreased testis weight	Ahr<tm1.2Arte>/Ahr<tm1.2Arte>	involves: C57BL/6NTac	N	24174576
MGI:5571486	M	MP:0002662	abnormal cauda epididymis morphology	Ahr<tm1.2Arte>/Ahr<tm1.2Arte>	involves: C57BL/6NTac	N	24174576
MGI:5571486	M	MP:0005578	teratozoospermia	Ahr<tm1.2Arte>/Ahr<tm1.2Arte>	involves: C57BL/6NTac	N	24174576
MGI:5571486	M	MP:0009647	decreased fertilization frequency	Ahr<tm1.2Arte>/Ahr<tm1.2Arte>	involves: C57BL/6NTac	N	24174576
MGI:5571486	M	MP:0001154	seminiferous tubule degeneration	Ahr<tm1.2Arte>/Ahr<tm1.2Arte>	involves: C57BL/6NTac	N	24174576
MGI:5571486	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Ahr<tm1.2Arte>/Ahr<tm1.2Arte>	involves: C57BL/6NTac	N	24174576
MGI:5571486	M	MP:0004182	abnormal spermiation	Ahr<tm1.2Arte>/Ahr<tm1.2Arte>	involves: C57BL/6NTac	N	24174576
MGI:5571486	M	MP:0020550	multinucleated giant male germ cells	Ahr<tm1.2Arte>/Ahr<tm1.2Arte>	involves: C57BL/6NTac	N	24174576
MGI:5571486	M	MP:0009238	coiled sperm flagellum	Ahr<tm1.2Arte>/Ahr<tm1.2Arte>	involves: C57BL/6NTac	N	24174576
MGI:5571486	M	MP:0008280	abnormal male germ cell apoptosis	Ahr<tm1.2Arte>/Ahr<tm1.2Arte>	involves: C57BL/6NTac	N	24174576
MGI:5571486	M	MP:0009230	abnormal sperm head morphology	Ahr<tm1.2Arte>/Ahr<tm1.2Arte>	involves: C57BL/6NTac	N	24174576
MGI:5571594	F	MP:0001923	reduced female fertility	Scd2<swty>/Scd2<swty>	C57BL/6JSfdAnu-Scd2<swty>/Anu	N	MGI:3611487
MGI:5571719	M	MP:0020356	abnormal Sertoli cell barrier function	Ar<tm2.1Reb>/Ar<+>,Tg(Amh-cre)8815Reb/?	129S(FVB)-Ar<tm2.1Reb>	N	24825397
MGI:5571719	M	MP:0020355	abnormal Sertoli cell barrier morphology	Ar<tm2.1Reb>/Ar<+>,Tg(Amh-cre)8815Reb/?	129S(FVB)-Ar<tm2.1Reb>	N	24825397
MGI:5572798	M	MP:0001922	reduced male fertility	Tshr<hyt-3J>/Tshr<hyt-3J>	CXB10/HiAJ-Tshr<hyt-3J>/GrsrJ	N	MGI:5571363
MGI:5572798	F	MP:0001923	reduced female fertility	Tshr<hyt-3J>/Tshr<hyt-3J>	CXB10/HiAJ-Tshr<hyt-3J>/GrsrJ	N	MGI:5571363
MGI:5572808	F	MP:0001923	reduced female fertility	Tshr<hyt-3J>/Tshr<hyt-3J>	CByJ;CXB10-Tshr<hyt-3J>/GrsrJ	N	MGI:5571363
MGI:5572808	M	MP:0001922	reduced male fertility	Tshr<hyt-3J>/Tshr<hyt-3J>	CByJ;CXB10-Tshr<hyt-3J>/GrsrJ	N	MGI:5571363
MGI:5572814	M	MP:0000603	pale liver	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572814	M	MP:0002079	increased circulating insulin level	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572814	M	MP:0005293	impaired glucose tolerance	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572814	M	MP:0003982	increased cholesterol level	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572814	M	MP:0000599	enlarged liver	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572814	M	MP:0005317	increased triglyceride level	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572814	M	MP:0001260	increased body weight	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572814	M	MP:0002628	hepatic steatosis	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572814	M	MP:0009288	increased epididymal fat pad weight	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572814	M	MP:0005290	decreased oxygen consumption	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572814	M	MP:0001264	increased body size	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572814	M	MP:0020234	decreased basal metabolism	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572814	M	MP:0009286	increased abdominal fat pad weight	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572814	M	MP:0001257	increased body length	Tg(Gh-Gal)4599Vron/Tg(Gh-Gal)4599Vron	B6.Cg-Tg(Gh-Gal)4599Vron	N	19773738
MGI:5572818	F	MP:0010505	abnormal T wave	Kcne3<tm1Gwab>/Kcne3<tm1Gwab>	involves: C57BL/6	N	24225147
MGI:5572818	F	MP:0003233	prolonged QT interval	Kcne3<tm1Gwab>/Kcne3<tm1Gwab>	involves: C57BL/6	N	24225147
MGI:5572833	M	MP:0005123	increased circulating growth hormone level	Tg(Gh-Gal)4599Vron/?	involves: C57BL/6 * CD-1 * SJL	N	14596666
MGI:5573176	M	MP:0003797	abnormal compact bone morphology	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0000195	decreased circulating calcium level	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0000065	abnormal bone marrow cavity morphology	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0010869	decreased bone trabecula number	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0000519	hydronephrosis	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0002764	short tibia	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0004993	decreased bone resorption	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0020040	decreased bone ossification	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0009346	decreased trabecular bone thickness	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0003109	short femur	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0001566	increased circulating phosphate level	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0010879	decreased trabecular bone volume	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0004991	decreased bone strength	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0010971	abnormal periosteum morphology	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0005390	skeleton phenotype	hydro/?	involves: Mlac:ICR	Y	24227694
MGI:5573176	M	MP:0010968	decreased compact bone area	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5573176	M	MP:0000063	decreased bone mineral density	hydro/?	involves: Mlac:ICR	N	24227694
MGI:5574068	M	MP:0005386	behavior/neurological phenotype	Cdkl5<tm1.1Cogr>/Y,Tg(dlx5a-cre)1Mekk/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * CD-1	Y	24838000
MGI:5574069	M	MP:0001402	decreased locomotor activity	Cdkl5<tm1.1Cogr>/?,Tg(dlx5a-cre)1Mekk/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * CD-1	N	24838000
MGI:5574069	M	MP:0005386	behavior/neurological phenotype	Cdkl5<tm1.1Cogr>/?,Tg(dlx5a-cre)1Mekk/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * CD-1	Y	24838000
MGI:5574070	F	MP:0001513	limb grasping	Cdkl5<tm1.1Cogr>/Cdkl5<+>,Tg(Emx1-cre)#Ito/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * C57BL/6J	N	24838000
MGI:5574070	F	MP:0005386	behavior/neurological phenotype	Cdkl5<tm1.1Cogr>/Cdkl5<+>,Tg(Emx1-cre)#Ito/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * C57BL/6J	Y	24838000
MGI:5574071	M	MP:0001513	limb grasping	Cdkl5<tm1.1Cogr>/Y,Tg(Emx1-cre)#Ito/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * C57BL/6J	N	24838000
MGI:5574071	M	MP:0005386	behavior/neurological phenotype	Cdkl5<tm1.1Cogr>/Y,Tg(Emx1-cre)#Ito/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * C57BL/6J	Y	24838000
MGI:5574072	F	MP:0001513	limb grasping	Cdkl5<tm1.2Cogr>/Cdkl5<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	N	24838000
MGI:5574072	F	MP:0010748	abnormal visual evoked potential	Cdkl5<tm1.2Cogr>/Cdkl5<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	N	24838000
MGI:5574072	F	MP:0001402	decreased locomotor activity	Cdkl5<tm1.2Cogr>/Cdkl5<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	N	24838000
MGI:5574073	F	MP:0010748	abnormal visual evoked potential	Cdkl5<tm1.2Cogr>/Cdkl5<tm1.2Cogr>	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	N	24838000
MGI:5574073	F	MP:0009357	abnormal seizure response to inducing agent	Cdkl5<tm1.2Cogr>/Cdkl5<tm1.2Cogr>	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	N	24838000
MGI:5574073	F	MP:0001513	limb grasping	Cdkl5<tm1.2Cogr>/Cdkl5<tm1.2Cogr>	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	N	24838000
MGI:5574073	F	MP:0002064	seizures	Cdkl5<tm1.2Cogr>/Cdkl5<tm1.2Cogr>	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	N	24838000
MGI:5574073	F	MP:0001402	decreased locomotor activity	Cdkl5<tm1.2Cogr>/Cdkl5<tm1.2Cogr>	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	N	24838000
MGI:5574074	M	MP:0001402	decreased locomotor activity	Cdkl5<tm1.2Cogr>/Y	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	N	24838000
MGI:5574074	M	MP:0001513	limb grasping	Cdkl5<tm1.2Cogr>/Y	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	N	24838000
MGI:5574074	M	MP:0002064	seizures	Cdkl5<tm1.2Cogr>/Y	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	N	24838000
MGI:5574074	M	MP:0009357	abnormal seizure response to inducing agent	Cdkl5<tm1.2Cogr>/Y	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	N	24838000
MGI:5574074	M	MP:0010748	abnormal visual evoked potential	Cdkl5<tm1.2Cogr>/Y	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	N	24838000
MGI:5574075	M	MP:0012444	thin hippocampus molecular cell layer	Cdkl5<tm1.2Cogr>/Y,Tg(Thy1-YFP)#Jrs/0	involves: 129P2/OlaHsd * 129S/Sv * C57BL/6J * CBA	N	24838000
MGI:5574075	M	MP:0000813	abnormal hippocampus layer morphology	Cdkl5<tm1.2Cogr>/Y,Tg(Thy1-YFP)#Jrs/0	involves: 129P2/OlaHsd * 129S/Sv * C57BL/6J * CBA	N	24838000
MGI:5574075	M	MP:0006254	thin cerebral cortex	Cdkl5<tm1.2Cogr>/Y,Tg(Thy1-YFP)#Jrs/0	involves: 129P2/OlaHsd * 129S/Sv * C57BL/6J * CBA	N	24838000
MGI:5574075	M	MP:0012446	thin hippocampus stratum oriens	Cdkl5<tm1.2Cogr>/Y,Tg(Thy1-YFP)#Jrs/0	involves: 129P2/OlaHsd * 129S/Sv * C57BL/6J * CBA	N	24838000
MGI:5574075	M	MP:0008143	abnormal dendrite morphology	Cdkl5<tm1.2Cogr>/Y,Tg(Thy1-YFP)#Jrs/0	involves: 129P2/OlaHsd * 129S/Sv * C57BL/6J * CBA	N	24838000
MGI:5574076	F	MP:0006254	thin cerebral cortex	Cdkl5<tm1.2Cogr>/Cdkl5<tm1.2Cogr>,Tg(Thy1-YFP)#Jrs/0	involves: 129P2/OlaHsd * 129S/Sv * C57BL/6J * CBA	N	24838000
MGI:5574076	F	MP:0012446	thin hippocampus stratum oriens	Cdkl5<tm1.2Cogr>/Cdkl5<tm1.2Cogr>,Tg(Thy1-YFP)#Jrs/0	involves: 129P2/OlaHsd * 129S/Sv * C57BL/6J * CBA	N	24838000
MGI:5574076	F	MP:0012444	thin hippocampus molecular cell layer	Cdkl5<tm1.2Cogr>/Cdkl5<tm1.2Cogr>,Tg(Thy1-YFP)#Jrs/0	involves: 129P2/OlaHsd * 129S/Sv * C57BL/6J * CBA	N	24838000
MGI:5574076	F	MP:0000813	abnormal hippocampus layer morphology	Cdkl5<tm1.2Cogr>/Cdkl5<tm1.2Cogr>,Tg(Thy1-YFP)#Jrs/0	involves: 129P2/OlaHsd * 129S/Sv * C57BL/6J * CBA	N	24838000
MGI:5574076	F	MP:0008143	abnormal dendrite morphology	Cdkl5<tm1.2Cogr>/Cdkl5<tm1.2Cogr>,Tg(Thy1-YFP)#Jrs/0	involves: 129P2/OlaHsd * 129S/Sv * C57BL/6J * CBA	N	24838000
MGI:5574077	F	MP:0008143	abnormal dendrite morphology	Cdkl5<tm1.2Cogr>/Cdkl5<+>,Tg(Thy1-YFP)#Jrs/0	involves: 129P2/OlaHsd * 129S/Sv * C57BL/6J * CBA	N	24838000
MGI:5574077	F	MP:0006254	thin cerebral cortex	Cdkl5<tm1.2Cogr>/Cdkl5<+>,Tg(Thy1-YFP)#Jrs/0	involves: 129P2/OlaHsd * 129S/Sv * C57BL/6J * CBA	N	24838000
MGI:5574284	F	MP:0003491	abnormal voluntary movement	Csmd1<tm1Lex>/Csmd1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6NTac	N	24244513
MGI:5574284	M	MP:0031391	increased locomotor activity	Csmd1<tm1Lex>/Csmd1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6NTac	N	24244513
MGI:5574339	m	MP:0005559	increased circulating glucose level	Prex2<Gt(AH0440)Wtsi>/Prex2<Gt(AH0440)Wtsi>	B6.129P2-Prex2<Gt(AH0440)Wtsi>	N	24367090
MGI:5574339	m	MP:0005293	impaired glucose tolerance	Prex2<Gt(AH0440)Wtsi>/Prex2<Gt(AH0440)Wtsi>	B6.129P2-Prex2<Gt(AH0440)Wtsi>	N	24367090
MGI:5574443	F	MP:0008883	abnormal enterocyte proliferation	Hprt1<tm1(CAG-NRIP1)Vcls>/Hprt1<+>	involves: 129 * C57BL/6	N	24667635
MGI:5574443	F	MP:0014234	decreased enterocyte apoptosis	Hprt1<tm1(CAG-NRIP1)Vcls>/Hprt1<+>	involves: 129 * C57BL/6	N	24667635
MGI:5574443	F	MP:0004843	abnormal Paneth cell morphology	Hprt1<tm1(CAG-NRIP1)Vcls>/Hprt1<+>	involves: 129 * C57BL/6	N	24667635
MGI:5574443	F	MP:0000496	abnormal small intestine morphology	Hprt1<tm1(CAG-NRIP1)Vcls>/Hprt1<+>	involves: 129 * C57BL/6	N	24667635
MGI:5574444	M	MP:0004843	abnormal Paneth cell morphology	Hprt1<tm1(CAG-NRIP1)Vcls>/Y	involves: 129 * C57BL/6	N	24667635
MGI:5574444	M	MP:0008883	abnormal enterocyte proliferation	Hprt1<tm1(CAG-NRIP1)Vcls>/Y	involves: 129 * C57BL/6	N	24667635
MGI:5574444	M	MP:0014234	decreased enterocyte apoptosis	Hprt1<tm1(CAG-NRIP1)Vcls>/Y	involves: 129 * C57BL/6	N	24667635
MGI:5574444	M	MP:0000496	abnormal small intestine morphology	Hprt1<tm1(CAG-NRIP1)Vcls>/Y	involves: 129 * C57BL/6	N	24667635
MGI:5574446	F	MP:0002083	premature death	Apc<tm1Cip>/Apc<+>,Nrip1<tm1Mpk>/Nrip1<+>	involves: 129P2/OlaHsd * C57BL/6J	N	24667635
MGI:5574447	m	MP:0001925	male infertility	Galntl5<tm1Nari>/Galntl5<+>	involves: 129P2/OlaHsd * C57BL/6J	N	24398516
MGI:5574447	m	MP:0002675	asthenozoospermia	Galntl5<tm1Nari>/Galntl5<+>	involves: 129P2/OlaHsd * C57BL/6J	N	24398516
MGI:5574447	m	MP:0005578	teratozoospermia	Galntl5<tm1Nari>/Galntl5<+>	involves: 129P2/OlaHsd * C57BL/6J	N	24398516
MGI:5574447	f	MP:0005389	reproductive system phenotype	Galntl5<tm1Nari>/Galntl5<+>	involves: 129P2/OlaHsd * C57BL/6J	Y	24398516
MGI:5574447	m	MP:0002687	oligozoospermia	Galntl5<tm1Nari>/Galntl5<+>	involves: 129P2/OlaHsd * C57BL/6J	N	24398516
MGI:5575488	M	MP:0008261	arrest of male meiosis	Kif18a<tm1Zgwg>/Kif18a<tm1Zgwg>	either: 129-Kif18a<tm1Zgwg> or (involves: 129 * C57BL/6J)	N	20981276
MGI:5575488	M	MP:0002216	abnormal seminiferous tubule morphology	Kif18a<tm1Zgwg>/Kif18a<tm1Zgwg>	either: 129-Kif18a<tm1Zgwg> or (involves: 129 * C57BL/6J)	N	20981276
MGI:5575488	M	MP:0000352	decreased cell proliferation	Kif18a<tm1Zgwg>/Kif18a<tm1Zgwg>	either: 129-Kif18a<tm1Zgwg> or (involves: 129 * C57BL/6J)	N	20981276
MGI:5575488	M	MP:0004046	abnormal mitosis	Kif18a<tm1Zgwg>/Kif18a<tm1Zgwg>	either: 129-Kif18a<tm1Zgwg> or (involves: 129 * C57BL/6J)	N	20981276
MGI:5575488	M	MP:0001925	male infertility	Kif18a<tm1Zgwg>/Kif18a<tm1Zgwg>	either: 129-Kif18a<tm1Zgwg> or (involves: 129 * C57BL/6J)	N	20981276
MGI:5575488	M	MP:0003205	testicular atrophy	Kif18a<tm1Zgwg>/Kif18a<tm1Zgwg>	either: 129-Kif18a<tm1Zgwg> or (involves: 129 * C57BL/6J)	N	20981276
MGI:5575488	M	MP:0003830	abnormal testis development	Kif18a<tm1Zgwg>/Kif18a<tm1Zgwg>	either: 129-Kif18a<tm1Zgwg> or (involves: 129 * C57BL/6J)	N	20981276
MGI:5575488	M	MP:0001154	seminiferous tubule degeneration	Kif18a<tm1Zgwg>/Kif18a<tm1Zgwg>	either: 129-Kif18a<tm1Zgwg> or (involves: 129 * C57BL/6J)	N	20981276
MGI:5575488	F	MP:0001923	reduced female fertility	Kif18a<tm1Zgwg>/Kif18a<tm1Zgwg>	either: 129-Kif18a<tm1Zgwg> or (involves: 129 * C57BL/6J)	N	20981276
MGI:5575488	M	MP:0001152	increased Leydig cell number	Kif18a<tm1Zgwg>/Kif18a<tm1Zgwg>	either: 129-Kif18a<tm1Zgwg> or (involves: 129 * C57BL/6J)	N	20981276
MGI:5575488	M	MP:0004852	decreased testis weight	Kif18a<tm1Zgwg>/Kif18a<tm1Zgwg>	either: 129-Kif18a<tm1Zgwg> or (involves: 129 * C57BL/6J)	N	20981276
MGI:5575488	M	MP:0014052	increased male germ cell apoptosis	Kif18a<tm1Zgwg>/Kif18a<tm1Zgwg>	either: 129-Kif18a<tm1Zgwg> or (involves: 129 * C57BL/6J)	N	20981276
MGI:5575651	M	MP:0004901	decreased male germ cell number	Chd5<tm1.2Gmbr>/Chd5<tm1.2Gmbr>	involves: 129S4/SvJae	N	24252660
MGI:5575651	M	MP:0008279	arrest of spermiogenesis	Chd5<tm1.2Gmbr>/Chd5<tm1.2Gmbr>	involves: 129S4/SvJae	N	24252660
MGI:5575651	M	MP:0001925	male infertility	Chd5<tm1.2Gmbr>/Chd5<tm1.2Gmbr>	involves: 129S4/SvJae	N	24252660
MGI:5575651	M	MP:0002675	asthenozoospermia	Chd5<tm1.2Gmbr>/Chd5<tm1.2Gmbr>	involves: 129S4/SvJae	N	24252660
MGI:5575651	M	MP:0004182	abnormal spermiation	Chd5<tm1.2Gmbr>/Chd5<tm1.2Gmbr>	involves: 129S4/SvJae	N	24252660
MGI:5575651	M	MP:0006380	abnormal spermatid morphology	Chd5<tm1.2Gmbr>/Chd5<tm1.2Gmbr>	involves: 129S4/SvJae	N	24252660
MGI:5575651	M	MP:0005578	teratozoospermia	Chd5<tm1.2Gmbr>/Chd5<tm1.2Gmbr>	involves: 129S4/SvJae	N	24252660
MGI:5575651	M	MP:0005376	homeostasis/metabolism phenotype	Chd5<tm1.2Gmbr>/Chd5<tm1.2Gmbr>	involves: 129S4/SvJae	Y	24252660
MGI:5575651	F	MP:0005389	reproductive system phenotype	Chd5<tm1.2Gmbr>/Chd5<tm1.2Gmbr>	involves: 129S4/SvJae	Y	24252660
MGI:5575651	M	MP:0001156	abnormal spermatogenesis	Chd5<tm1.2Gmbr>/Chd5<tm1.2Gmbr>	involves: 129S4/SvJae	N	24252660
MGI:5575651	M	MP:0006362	abnormal male germ cell morphology	Chd5<tm1.2Gmbr>/Chd5<tm1.2Gmbr>	involves: 129S4/SvJae	N	24252660
MGI:5575651	M	MP:0002687	oligozoospermia	Chd5<tm1.2Gmbr>/Chd5<tm1.2Gmbr>	involves: 129S4/SvJae	N	24252660
MGI:5575773	F	MP:0001513	limb grasping	Tardbp<m1H>/Tardbp<+>	involves: C3H/HeH * C57BL/6J	N	24465814
MGI:5575779	M	MP:0001262	decreased body weight	Adcy3<Jll>/Adcy3<+>	C57BL/6J-Adcy3<Jll>	N	25329148
MGI:5575779	M	MP:0010025	decreased total body fat amount	Adcy3<Jll>/Adcy3<+>	C57BL/6J-Adcy3<Jll>	N	25329148
MGI:5575781	M	MP:0001399	hyperactivity	Adcy3<Jll>/Adcy3<+>	involves: 129S1/SvImJ * C57BL/6J	N	25329148
MGI:5575781	M	MP:0005289	increased oxygen consumption	Adcy3<Jll>/Adcy3<+>	involves: 129S1/SvImJ * C57BL/6J	N	25329148
MGI:5575781	M	MP:0005560	decreased circulating glucose level	Adcy3<Jll>/Adcy3<+>	involves: 129S1/SvImJ * C57BL/6J	N	25329148
MGI:5576197	M	MP:0005386	behavior/neurological phenotype	Deaf1<tm1.1Mico>/Deaf1<tm1.1Mico>,Tg(Nes-cre)1Kln/0	involves: 129 * C57BL/6 * SJL	Y	24726472
MGI:5576197	M	MP:0003460	decreased fear-related response	Deaf1<tm1.1Mico>/Deaf1<tm1.1Mico>,Tg(Nes-cre)1Kln/0	involves: 129 * C57BL/6 * SJL	N	24726472
MGI:5576197	M	MP:0012306	enhanced spatial learning	Deaf1<tm1.1Mico>/Deaf1<tm1.1Mico>,Tg(Nes-cre)1Kln/0	involves: 129 * C57BL/6 * SJL	N	24726472
MGI:5576239	M	MP:0001925	male infertility	Gt(ROSA)26Sor<tm1(DTA)Lky>/Gt(ROSA)26Sor<+>,Tg(LHX3-cre)#Sjr/0	involves: 129P2/OlaHsd * BALB/c * C3H * C57BL/6	N	24100213
MGI:5576342	M	MP:0005389	reproductive system phenotype	Gnrhr<tm1.1Bhr>/Gnrhr<tm1.1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	Y	22918878
MGI:5576342	F	MP:0002680	decreased corpora lutea number	Gnrhr<tm1.1Bhr>/Gnrhr<tm1.1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	22918878
MGI:5576342	M	MP:0001145	abnormal male reproductive system morphology	Gnrhr<tm1.1Bhr>/Gnrhr<tm1.1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	22918878
MGI:5576342	F	MP:0001126	abnormal ovary morphology	Gnrhr<tm1.1Bhr>/Gnrhr<tm1.1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	22918878
MGI:5576342	F	MP:0009017	prolonged estrus	Gnrhr<tm1.1Bhr>/Gnrhr<tm1.1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	22918878
MGI:5576342	M	MP:0001147	small testis	Gnrhr<tm1.1Bhr>/Gnrhr<tm1.1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	22918878
MGI:5576342	F	MP:0011128	increased tertiary ovarian follicle number	Gnrhr<tm1.1Bhr>/Gnrhr<tm1.1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	22918878
MGI:5576343	F	MP:0001129	impaired ovarian folliculogenesis	Gnrhr<tm1Bhr>/Gnrhr<tm1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	24324164
MGI:5576343	M	MP:0002687	oligozoospermia	Gnrhr<tm1Bhr>/Gnrhr<tm1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	24324164
MGI:5576343	F	MP:0001127	small ovary	Gnrhr<tm1Bhr>/Gnrhr<tm1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	24324164
MGI:5576343	M	MP:0001929	abnormal gametogenesis	Gnrhr<tm1Bhr>/Gnrhr<tm1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	24324164
MGI:5576343	M	MP:0001153	small seminiferous tubules	Gnrhr<tm1Bhr>/Gnrhr<tm1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	24324164
MGI:5576343	F	MP:0001126	abnormal ovary morphology	Gnrhr<tm1Bhr>/Gnrhr<tm1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	24324164
MGI:5576343	M	MP:0001147	small testis	Gnrhr<tm1Bhr>/Gnrhr<tm1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	24324164
MGI:5576343	M	MP:0008892	abnormal sperm flagellum morphology	Gnrhr<tm1Bhr>/Gnrhr<tm1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	24324164
MGI:5576343	M	MP:0009234	absent sperm head	Gnrhr<tm1Bhr>/Gnrhr<tm1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	24324164
MGI:5576343	M	MP:0005578	teratozoospermia	Gnrhr<tm1Bhr>/Gnrhr<tm1Bhr>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	24324164
MGI:5576345	F	MP:0001127	small ovary	Gnrhr<hh>/Gnrhr<hh>	involves: C57BL/6	N	22918878
MGI:5576345	M	MP:0004852	decreased testis weight	Gnrhr<hh>/Gnrhr<hh>	involves: C57BL/6	N	22918878
MGI:5576345	M	MP:0002786	abnormal Leydig cell morphology	Gnrhr<hh>/Gnrhr<hh>	involves: C57BL/6	N	22918878
MGI:5576345	M	MP:0001155	arrest of spermatogenesis	Gnrhr<hh>/Gnrhr<hh>	involves: C57BL/6	N	22918878
MGI:5576345	M	MP:0001147	small testis	Gnrhr<hh>/Gnrhr<hh>	involves: C57BL/6	N	22918878
MGI:5576345	M	MP:0001145	abnormal male reproductive system morphology	Gnrhr<hh>/Gnrhr<hh>	involves: C57BL/6	N	22918878
MGI:5576345	F	MP:0009009	absent estrous cycle	Gnrhr<hh>/Gnrhr<hh>	involves: C57BL/6	N	22918878
MGI:5576345	M	MP:0002773	decreased circulating luteinizing hormone level	Gnrhr<hh>/Gnrhr<hh>	involves: C57BL/6	N	22918878
MGI:5576345	M	MP:0002790	decreased circulating follicle stimulating hormone level	Gnrhr<hh>/Gnrhr<hh>	involves: C57BL/6	N	22918878
MGI:5576345	F	MP:0001129	impaired ovarian folliculogenesis	Gnrhr<hh>/Gnrhr<hh>	involves: C57BL/6	N	22918878
MGI:5576345	M	MP:0001925	male infertility	Gnrhr<hh>/Gnrhr<hh>	involves: C57BL/6	N	22918878
MGI:5576345	F	MP:0001126	abnormal ovary morphology	Gnrhr<hh>/Gnrhr<hh>	involves: C57BL/6	N	22918878
MGI:5576388	M	MP:0005584	abnormal enzyme/coenzyme activity	Tmbim1<tm1Noj>/Tmbim1<tm1Noj>	B6.129S2-Tmbim1<tm1Noj>	N	16636500
MGI:5576388	M	MP:0010574	dilated aorta	Tmbim1<tm1Noj>/Tmbim1<tm1Noj>	B6.129S2-Tmbim1<tm1Noj>	N	16636500
MGI:5576388	M	MP:0001570	abnormal circulating enzyme level	Tmbim1<tm1Noj>/Tmbim1<tm1Noj>	B6.129S2-Tmbim1<tm1Noj>	N	16636500
MGI:5576392	M	MP:0000186	decreased circulating HDL cholesterol level	Ppard<tm1(PPARD)Bsls>/Ppard<tm1(PPARD)Bsls>	B6.Cg-Ppard<tm1(PPARD)Bsls>	N	21426320
MGI:5576392	M	MP:0005179	decreased circulating cholesterol level	Ppard<tm1(PPARD)Bsls>/Ppard<tm1(PPARD)Bsls>	B6.Cg-Ppard<tm1(PPARD)Bsls>	N	21426320
MGI:5576392	F	MP:0000189	hypoglycemia	Ppard<tm1(PPARD)Bsls>/Ppard<tm1(PPARD)Bsls>	B6.Cg-Ppard<tm1(PPARD)Bsls>	N	21426320
MGI:5576513	M	MP:0000230	abnormal systemic arterial blood pressure	Timp1<tm1Pds>/Y	involves: 129S4/SvJae * C57BL/6	N	23524300
MGI:5576513	M	MP:0005385	cardiovascular system phenotype	Timp1<tm1Pds>/Y	involves: 129S4/SvJae * C57BL/6	Y	23524300
MGI:5576517	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(Wap-Hgf)402Mig/0	involves: FVB/N	N	14627990
MGI:5576517	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(Wap-Hgf)402Mig/0	involves: FVB/N	N	14627990
MGI:5576517	F	MP:0001885	mammary gland duct hyperplasia	Tg(Wap-Hgf)402Mig/0	involves: FVB/N	N	14627990
MGI:5576517	F	MP:0001272	increased metastatic potential	Tg(Wap-Hgf)402Mig/0	involves: FVB/N	N	14627990
MGI:5576517	F	MP:0012571	increased mammary gland tumor incidence in virgin females	Tg(Wap-Hgf)402Mig/0	involves: FVB/N	N	14627990
MGI:5576517	F	MP:0000627	abnormal mammary gland morphology	Tg(Wap-Hgf)402Mig/0	involves: FVB/N	N	14627990
MGI:5576517	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(Wap-Hgf)402Mig/0	involves: FVB/N	N	14627990
MGI:5576520	F	MP:0000627	abnormal mammary gland morphology	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Tg(Wap-cre)11738Mam/0,Tg(Wap-Hgf)402Mig/0	FVB.Cg-Ctnnb1<tm1Mmt> Tg(Wap-cre)11738Mam Tg(Wap-Hgf)402Mig	N	24290754
MGI:5576520	F	MP:0001884	mammary gland alveolar hyperplasia	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Tg(Wap-cre)11738Mam/0,Tg(Wap-Hgf)402Mig/0	FVB.Cg-Ctnnb1<tm1Mmt> Tg(Wap-cre)11738Mam Tg(Wap-Hgf)402Mig	N	24290754
MGI:5576520	F	MP:0006270	abnormal mammary gland growth during lactation	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Tg(Wap-cre)11738Mam/0,Tg(Wap-Hgf)402Mig/0	FVB.Cg-Ctnnb1<tm1Mmt> Tg(Wap-cre)11738Mam Tg(Wap-Hgf)402Mig	N	24290754
MGI:5576520	F	MP:0012571	increased mammary gland tumor incidence in virgin females	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Tg(Wap-cre)11738Mam/0,Tg(Wap-Hgf)402Mig/0	FVB.Cg-Ctnnb1<tm1Mmt> Tg(Wap-cre)11738Mam Tg(Wap-Hgf)402Mig	N	24290754
MGI:5576520	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Tg(Wap-cre)11738Mam/0,Tg(Wap-Hgf)402Mig/0	FVB.Cg-Ctnnb1<tm1Mmt> Tg(Wap-cre)11738Mam Tg(Wap-Hgf)402Mig	N	24290754
MGI:5576521	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Tg(Wap-cre)11738Mam/0	FVB.Cg-Ctnnb1<tm1Mmt> Tg(Wap-cre)11738Mam	N	24290754
MGI:5576522	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(Wap-Hgf)402Mig/0	FVB/N-Tg(Wap-Hgf)402Mig	N	24290754
MGI:5576522	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(Wap-Hgf)402Mig/0	FVB/N-Tg(Wap-Hgf)402Mig	N	24290754
MGI:5576532	F	MP:0012568	decreased mammary gland tumor incidence in breeding females	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Cxcr4<tm2Yzo>/Cxcr4<tm2Yzo>,Tg(Wap-cre)11738Mam/0,Tg(Wap-Hgf)402Mig/0	FVB.Cg-Cxcr4<tm2Yzo> Ctnnb1<tm1Mmt> Tg(Wap-cre)11738Mam Tg(Wap-Hgf)402Mig	N	24290754
MGI:5576721	F	MP:0002021	increased incidence of induced tumors	Prf1<tm1Sdz>/Prf1<tm1Sdz>	A.B6-Prf1<tm1Sdz>	N	24658838
MGI:5576721	F	MP:0005070	impaired natural killer cell mediated cytotoxicity	Prf1<tm1Sdz>/Prf1<tm1Sdz>	A.B6-Prf1<tm1Sdz>	N	24658838
MGI:5576722	F	MP:0005070	impaired natural killer cell mediated cytotoxicity	Prf1<tm1Sdz>/Prf1<+>	A.B6-Prf1<tm1Sdz>	N	24658838
MGI:5576722	F	MP:0002021	increased incidence of induced tumors	Prf1<tm1Sdz>/Prf1<+>	A.B6-Prf1<tm1Sdz>	N	24658838
MGI:5576750	M	MP:0005559	increased circulating glucose level	Cep19<tm2.1Jmgi>/Cep19<tm2.1Jmgi>	involves: C57BL/6NTac	N	24268657
MGI:5576780	M	MP:0020451	decreased sperm progressive motility	Ros1<tm1.1Char>/Ros1<tm1.1Char>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * SJL	N	24971615
MGI:5576780	M	MP:0002675	asthenozoospermia	Ros1<tm1.1Char>/Ros1<tm1.1Char>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * SJL	N	24971615
MGI:5576780	M	MP:0001925	male infertility	Ros1<tm1.1Char>/Ros1<tm1.1Char>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * SJL	N	24971615
MGI:5576780	M	MP:0009243	hairpin sperm flagellum	Ros1<tm1.1Char>/Ros1<tm1.1Char>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * SJL	N	24971615
MGI:5576780	M	MP:0004933	abnormal epididymis epithelium morphology	Ros1<tm1.1Char>/Ros1<tm1.1Char>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * SJL	N	24971615
MGI:5576898	M	MP:0001925	male infertility	Ppargc1a<tm2Brsp>/Ppargc1a<tm2Brsp>	involves: 129	N	17932564
MGI:5576932	M	MP:0005379	endocrine/exocrine gland phenotype	Hprt1<tm1(TG-cre)1Sasr>/Y	involves: C57BL/6	Y	24265449
MGI:5576932	M	MP:0005378	growth/size/body region phenotype	Hprt1<tm1(TG-cre)1Sasr>/Y	involves: C57BL/6	Y	24265449
MGI:5576933	M	MP:0005477	increased circulating thyroxine level	Thrb<tm1Mkni>/Thrb<tm1Mkni>,Hprt1<tm1(TG-cre)1Sasr>/Y	involves: 129/Sv * C57BL/6	N	24265449
MGI:5576933	M	MP:0005468	abnormal thyroid hormone level	Thrb<tm1Mkni>/Thrb<tm1Mkni>,Hprt1<tm1(TG-cre)1Sasr>/Y	involves: 129/Sv * C57BL/6	N	24265449
MGI:5576933	M	MP:0005119	decreased circulating thyroid-stimulating hormone level	Thrb<tm1Mkni>/Thrb<tm1Mkni>,Hprt1<tm1(TG-cre)1Sasr>/Y	involves: 129/Sv * C57BL/6	N	24265449
MGI:5576933	M	MP:0005378	growth/size/body region phenotype	Thrb<tm1Mkni>/Thrb<tm1Mkni>,Hprt1<tm1(TG-cre)1Sasr>/Y	involves: 129/Sv * C57BL/6	Y	24265449
MGI:5576933	M	MP:0003350	increased circulating levels of thyroid hormone	Thrb<tm1Mkni>/Thrb<tm1Mkni>,Hprt1<tm1(TG-cre)1Sasr>/Y	involves: 129/Sv * C57BL/6	N	24265449
MGI:5576933	M	MP:0020168	decreased thyroid gland weight	Thrb<tm1Mkni>/Thrb<tm1Mkni>,Hprt1<tm1(TG-cre)1Sasr>/Y	involves: 129/Sv * C57BL/6	N	24265449
MGI:5576933	M	MP:0005470	increased thyroxine level	Thrb<tm1Mkni>/Thrb<tm1Mkni>,Hprt1<tm1(TG-cre)1Sasr>/Y	involves: 129/Sv * C57BL/6	N	24265449
MGI:5576972	M	MP:0005385	cardiovascular system phenotype	Hprt1<tm3(CAG-Tbx18,-Venus)Akis>/Y,Tbx18<tm4(cre)Akis>/Tbx18<+>	involves: 129S1/SvImJ * NMRI	Y	22926762
MGI:5576972	M	MP:0011085	postnatal lethality, complete penetrance	Hprt1<tm3(CAG-Tbx18,-Venus)Akis>/Y,Tbx18<tm4(cre)Akis>/Tbx18<+>	involves: 129S1/SvImJ * NMRI	N	22926762
MGI:5576973	M	MP:0031590	abnormal epicardium development	Hprt1<tm4(CAG-Tbx18*,-Venus)Akis>/Y,Gt(ROSA)26Sor<tm4(ACTB-tdTomato,-EGFP)Luo>/Gt(ROSA)26Sor<+>,Tbx18<tm4(cre)Akis>/Tbx18<+>	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * NMRI	N	22926762
MGI:5576974	M	MP:0000288	abnormal pericardium morphology	Hprt1<tm4(CAG-Tbx18*,-Venus)Akis>/Y,Tbx18<tm4(cre)Akis>/Tbx18<+>	involves: 129S1/SvImJ * NMRI	N	22926762
MGI:5576974	M	MP:0003228	abnormal sinus venosus morphology	Hprt1<tm4(CAG-Tbx18*,-Venus)Akis>/Y,Tbx18<tm4(cre)Akis>/Tbx18<+>	involves: 129S1/SvImJ * NMRI	N	22926762
MGI:5576974	M	MP:0005385	cardiovascular system phenotype	Hprt1<tm4(CAG-Tbx18*,-Venus)Akis>/Y,Tbx18<tm4(cre)Akis>/Tbx18<+>	involves: 129S1/SvImJ * NMRI	Y	22926762
MGI:5576974	M	MP:0002740	heart hypoplasia	Hprt1<tm4(CAG-Tbx18*,-Venus)Akis>/Y,Tbx18<tm4(cre)Akis>/Tbx18<+>	involves: 129S1/SvImJ * NMRI	N	22926762
MGI:5576974	M	MP:0010556	thin ventricle myocardium compact layer	Hprt1<tm4(CAG-Tbx18*,-Venus)Akis>/Y,Tbx18<tm4(cre)Akis>/Tbx18<+>	involves: 129S1/SvImJ * NMRI	N	22926762
MGI:5576974	M	MP:0011395	decreased fetal cardiomyocyte proliferation	Hprt1<tm4(CAG-Tbx18*,-Venus)Akis>/Y,Tbx18<tm4(cre)Akis>/Tbx18<+>	involves: 129S1/SvImJ * NMRI	N	22926762
MGI:5576974	M	MP:0011099	lethality throughout fetal growth and development, complete penetrance	Hprt1<tm4(CAG-Tbx18*,-Venus)Akis>/Y,Tbx18<tm4(cre)Akis>/Tbx18<+>	involves: 129S1/SvImJ * NMRI	N	22926762
MGI:5577072	M	MP:0000436	abnormal head movements	Il6<tm1.1Jho>/Il6<tm1.1Jho>,Tg(GFAP-cre)8Gtm/0	involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA	N	23085146
MGI:5577072	M	MP:0001260	increased body weight	Il6<tm1.1Jho>/Il6<tm1.1Jho>,Tg(GFAP-cre)8Gtm/0	involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA	N	23085146
MGI:5577073	F	MP:0001402	decreased locomotor activity	Il6<tm1.1Jho>/Il6<+>,Tg(GFAP-cre)8Gtm/0	involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA	N	23085146
MGI:5577140	M	MP:0008892	abnormal sperm flagellum morphology	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577140	M	MP:0009836	abnormal sperm principal piece morphology	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577140	M	MP:0009230	abnormal sperm head morphology	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577140	M	MP:0005389	reproductive system phenotype	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	Y	24525297
MGI:5577140	M	MP:0009838	abnormal sperm axoneme morphology	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577140	M	MP:0009376	abnormal manchette morphology	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577140	M	MP:0009232	abnormal sperm nucleus morphology	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577140	M	MP:0009234	absent sperm head	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577140	M	MP:0031386	elongated manchette	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577140	M	MP:0009280	decreased activated sperm motility	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577140	M	MP:0001925	male infertility	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577140	M	MP:0002687	oligozoospermia	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577140	M	MP:0006380	abnormal spermatid morphology	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577140	M	MP:0030590	abnormal sperm fibrous sheath morphology	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577140	M	MP:0020451	decreased sperm progressive motility	Stk36<tm1Ptch>/Stk36<tm1Ptch>,Tg(Ddx4-cre)1Ptch/0	involves: 129P2/OlaHsd	N	24525297
MGI:5577255	M	MP:0001399	hyperactivity	Elfn1<tm1(KOMP)Vlcg>/Elfn1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	24312227
MGI:5578156	M	MP:0003447	decreased tumor growth/size	Idh2<tm1Jwpk>/Idh2<tm1Jwpk>	involves: 129S4/SvJae * C57BL/6	N	24240089
MGI:5578156	M	MP:0010639	abnormal tumor pathology	Idh2<tm1Jwpk>/Idh2<tm1Jwpk>	involves: 129S4/SvJae * C57BL/6	N	24240089
MGI:5578156	M	MP:0010144	abnormal tumor vascularization	Idh2<tm1Jwpk>/Idh2<tm1Jwpk>	involves: 129S4/SvJae * C57BL/6	N	24240089
MGI:5578173	M	MP:0003324	increased liver adenoma incidence	Tg(HBV-HCV)21Kko/0	C57BL/6N-Tg(HBV-HCV)21Kko	N	9734402
MGI:5578173	M	MP:0011634	abnormal mitochondrial inner membrane morphology	Tg(HBV-HCV)21Kko/0	C57BL/6N-Tg(HBV-HCV)21Kko	N	9734402
MGI:5578173	M	MP:0002628	hepatic steatosis	Tg(HBV-HCV)21Kko/0	C57BL/6N-Tg(HBV-HCV)21Kko	N	9734402
MGI:5578173	M	MP:0003331	increased hepatocellular carcinoma incidence	Tg(HBV-HCV)21Kko/0	C57BL/6N-Tg(HBV-HCV)21Kko	N	9734402
MGI:5578175	M	MP:0002628	hepatic steatosis	Tg(HBV-HCV)49Kko/0	C57BL/6N-Tg(HBV-HCV)49Kko	N	9734402
MGI:5578175	M	MP:0011634	abnormal mitochondrial inner membrane morphology	Tg(HBV-HCV)49Kko/0	C57BL/6N-Tg(HBV-HCV)49Kko	N	9734402
MGI:5578175	M	MP:0003331	increased hepatocellular carcinoma incidence	Tg(HBV-HCV)49Kko/0	C57BL/6N-Tg(HBV-HCV)49Kko	N	9734402
MGI:5578175	M	MP:0003324	increased liver adenoma incidence	Tg(HBV-HCV)49Kko/0	C57BL/6N-Tg(HBV-HCV)49Kko	N	9734402
MGI:5578176	M	MP:0011593	increased catalase activity	Tg(HBV-HCV)Kko/0	C57BL/6N-Tg(HBV-HCV)Kko	N	11389061
MGI:5578176	M	MP:0011634	abnormal mitochondrial inner membrane morphology	Tg(HBV-HCV)Kko/0	C57BL/6N-Tg(HBV-HCV)Kko	N	11389061
MGI:5578176	M	MP:0003674	oxidative stress	Tg(HBV-HCV)Kko/0	C57BL/6N-Tg(HBV-HCV)Kko	N	11389061
MGI:5578176	M	MP:0011634	abnormal mitochondrial inner membrane morphology	Tg(HBV-HCV)Kko/0	C57BL/6N-Tg(HBV-HCV)Kko	N	9734402
MGI:5578176	M	MP:0003331	increased hepatocellular carcinoma incidence	Tg(HBV-HCV)Kko/0	C57BL/6N-Tg(HBV-HCV)Kko	N	9734402
MGI:5578176	M	MP:0003324	increased liver adenoma incidence	Tg(HBV-HCV)Kko/0	C57BL/6N-Tg(HBV-HCV)Kko	N	9734402
MGI:5578176	M	MP:0000609	abnormal liver physiology	Tg(HBV-HCV)Kko/0	C57BL/6N-Tg(HBV-HCV)Kko	N	11389061
MGI:5578176	M	MP:0012604	decreased glutathione level	Tg(HBV-HCV)Kko/0	C57BL/6N-Tg(HBV-HCV)Kko	N	11389061
MGI:5578176	M	MP:0000607	abnormal hepatocyte morphology	Tg(HBV-HCV)Kko/0	C57BL/6N-Tg(HBV-HCV)Kko	N	11389061
MGI:5578176	M	MP:0002628	hepatic steatosis	Tg(HBV-HCV)Kko/0	C57BL/6N-Tg(HBV-HCV)Kko	N	9734402
MGI:5578324	F	MP:0013507	increased ovary apoptosis	Tet1<Gt(RRG140)Byg>/Tet1<Gt(RRG140)Byg>	B6.129P2-Tet1<Gt(RRG140)Byg>	N	23151479
MGI:5578324	F	MP:0001127	small ovary	Tet1<Gt(RRG140)Byg>/Tet1<Gt(RRG140)Byg>	B6.129P2-Tet1<Gt(RRG140)Byg>	N	23151479
MGI:5578324	F	MP:0004856	decreased ovary weight	Tet1<Gt(RRG140)Byg>/Tet1<Gt(RRG140)Byg>	B6.129P2-Tet1<Gt(RRG140)Byg>	N	23151479
MGI:5578324	F	MP:0003578	absent ovary	Tet1<Gt(RRG140)Byg>/Tet1<Gt(RRG140)Byg>	B6.129P2-Tet1<Gt(RRG140)Byg>	N	23151479
MGI:5578324	F	MP:0005168	abnormal female meiosis	Tet1<Gt(RRG140)Byg>/Tet1<Gt(RRG140)Byg>	B6.129P2-Tet1<Gt(RRG140)Byg>	N	23151479
MGI:5578324	F	MP:0010948	abnormal double-strand DNA break repair	Tet1<Gt(RRG140)Byg>/Tet1<Gt(RRG140)Byg>	B6.129P2-Tet1<Gt(RRG140)Byg>	N	23151479
MGI:5578324	F	MP:0009452	abnormal synaptonemal complex	Tet1<Gt(RRG140)Byg>/Tet1<Gt(RRG140)Byg>	B6.129P2-Tet1<Gt(RRG140)Byg>	N	23151479
MGI:5578324	F	MP:0005431	decreased oocyte number	Tet1<Gt(RRG140)Byg>/Tet1<Gt(RRG140)Byg>	B6.129P2-Tet1<Gt(RRG140)Byg>	N	23151479
MGI:5578324	M	MP:0005389	reproductive system phenotype	Tet1<Gt(RRG140)Byg>/Tet1<Gt(RRG140)Byg>	B6.129P2-Tet1<Gt(RRG140)Byg>	Y	23151479
MGI:5578346	M	MP:0010869	decreased bone trabecula number	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	15109498
MGI:5578346	M	MP:0004016	decreased bone mass	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	15109498
MGI:5578346	M	MP:0004033	supernumerary teeth	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	24416220
MGI:5578346	M	MP:0003932	abnormal molar crown morphology	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	24416220
MGI:5578346	M	MP:0030536	abnormal diastema morphology	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	24416220
MGI:5578346	M	MP:0002896	abnormal bone mineralization	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	15109498
MGI:5578346	M	MP:0030388	large fontanelles	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	15109498
MGI:5578346	M	MP:0030029	wide cranial sutures	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	15109498
MGI:5578346	M	MP:0004377	small frontal bone	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	15109498
MGI:5578346	M	MP:0004380	short frontal bone	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	24416220
MGI:5578346	M	MP:0004384	small interparietal bone	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	15109498
MGI:5578346	M	MP:0004418	small parietal bone	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	15109498
MGI:5578346	M	MP:0003723	abnormal long bone morphology	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	15109498
MGI:5578346	M	MP:0004610	small vertebrae	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	15109498
MGI:5578346	M	MP:0004686	decreased length of long bones	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	15109498
MGI:5578346	M	MP:0011165	abnormal tooth root development	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	24416220
MGI:5578346	M	MP:0002100	abnormal tooth morphology	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	24416220
MGI:5578346	M	MP:0011862	decreased cranium length	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	24416220
MGI:5578346	M	MP:0002689	abnormal molar morphology	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	24416220
MGI:5578346	M	MP:0008271	abnormal bone ossification	Rps6ka3<tm1.1Kry>/Y	involves: 129X1/SvJ	N	15109498
MGI:5578564	M	MP:0001925	male infertility	Grid2<ho-18J>/Grid2<ho-18J>	B6.Cg-Grid2<ho-18J>/GrsrJ	N	MGI:5578534
MGI:5578645	M	MP:0005389	reproductive system phenotype	Tmprss2<tm1.1(ERG)Sho>/Tmprss2<tm1.1(ERG)Sho>	involves: C57BL/6 * DBA/2	Y	23512661
MGI:5578645	M	MP:0002006	neoplasm	Tmprss2<tm1.1(ERG)Sho>/Tmprss2<tm1.1(ERG)Sho>	involves: C57BL/6 * DBA/2	Y	23512661
MGI:5578646	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1.1Hwu>/Pten<+>,Tmprss2<tm1.1(ERG)Sho>/Tmprss2<tm1.1(ERG)Sho>	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	23512661
MGI:5578647	M	MP:0005389	reproductive system phenotype	Tmprss2<tm2.1(ETV1)Sho>/Tmprss2<tm2.1(ETV1)Sho>	involves: C57BL/6 * DBA/2	Y	23512661
MGI:5578647	M	MP:0003608	prostate gland inflammation	Tmprss2<tm2.1(ETV1)Sho>/Tmprss2<tm2.1(ETV1)Sho>	involves: C57BL/6 * DBA/2	N	23512661
MGI:5578647	M	MP:0002006	neoplasm	Tmprss2<tm2.1(ETV1)Sho>/Tmprss2<tm2.1(ETV1)Sho>	involves: C57BL/6 * DBA/2	Y	23512661
MGI:5578647	M	MP:0011385	abnormal testosterone level	Tmprss2<tm2.1(ETV1)Sho>/Tmprss2<tm2.1(ETV1)Sho>	involves: C57BL/6 * DBA/2	N	23512661
MGI:5578648	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1.1Hwu>/Pten<+>,Tmprss2<tm2.1(ETV1)Sho>/Tmprss2<tm2.1(ETV1)Sho>	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	23512661
MGI:5578649	M	MP:0009737	prostate gland cyst	Pten<tm1Hwu>/Pten<+>,Tmprss2<tm2.1(ETV1)Sho>/Tmprss2<tm2.1(ETV1)Sho>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	23512661
MGI:5578649	M	MP:0002083	premature death	Pten<tm1Hwu>/Pten<+>,Tmprss2<tm2.1(ETV1)Sho>/Tmprss2<tm2.1(ETV1)Sho>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	23512661
MGI:5578649	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Hwu>/Pten<+>,Tmprss2<tm2.1(ETV1)Sho>/Tmprss2<tm2.1(ETV1)Sho>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	23512661
MGI:5578650	M	MP:0002006	neoplasm	Del(16Tmprss2-Erg)1Sho/Del(16Tmprss2-Erg)1Sho	involves: C57BL/6 * DBA/2	Y	23512661
MGI:5578650	M	MP:0000659	prostate gland hyperplasia	Del(16Tmprss2-Erg)1Sho/Del(16Tmprss2-Erg)1Sho	involves: C57BL/6 * DBA/2	N	23512661
MGI:5578651	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Del(16Tmprss2-Erg)1Sho/Del(16Tmprss2-Erg)1Sho,Pten<tm1.1Hwu>/Pten<+>	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	23512661
MGI:5578652	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Erg<tm1.1Sho>/Erg<tm1.1Sho>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tmprss2<tm3Sho>/Tmprss2<tm3Sho>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	23512661
MGI:5578652	M	MP:0010768	mortality/aging	Erg<tm1.1Sho>/Erg<tm1.1Sho>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tmprss2<tm3Sho>/Tmprss2<tm3Sho>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	Y	23512661
MGI:5578736	F	MP:0001260	increased body weight	Crh<m1H>/Crh<+>	involves: C3H/HeH * C57BL/6J	N	24302625
MGI:5578736	F	MP:0005553	increased circulating creatinine level	Crh<m1H>/Crh<+>	involves: C3H/HeH * C57BL/6J	N	24302625
MGI:5578736	F	MP:0005568	increased circulating total protein level	Crh<m1H>/Crh<+>	involves: C3H/HeH * C57BL/6J	N	24302625
MGI:5578736	M	MP:0001426	polydipsia	Crh<m1H>/Crh<+>	involves: C3H/HeH * C57BL/6J	N	24302625
MGI:5578736	M	MP:0001262	decreased body weight	Crh<m1H>/Crh<+>	involves: C3H/HeH * C57BL/6J	N	24302625
MGI:5578736	M	MP:0005343	increased circulating aspartate transaminase level	Crh<m1H>/Crh<+>	involves: C3H/HeH * C57BL/6J	N	24302625
MGI:5578736	F	MP:0008821	increased blood uric acid level	Crh<m1H>/Crh<+>	involves: C3H/HeH * C57BL/6J	N	24302625
MGI:5581656	M	MP:0012370	decreased erythrocyte potassium level	Kel<tm1Slee>/Kel<tm1Slee>	B6.129X1-Kel<tm1Slee>	N	23122227
MGI:5581656	M	MP:0008850	increased hemoglobin concentration distribution width	Kel<tm1Slee>/Kel<tm1Slee>	B6.129X1-Kel<tm1Slee>	N	23122227
MGI:5581656	M	MP:0012367	decreased erythrocyte magnesium level	Kel<tm1Slee>/Kel<tm1Slee>	B6.129X1-Kel<tm1Slee>	N	23122227
MGI:5581656	M	MP:0002640	reticulocytosis	Kel<tm1Slee>/Kel<tm1Slee>	B6.129X1-Kel<tm1Slee>	N	23122227
MGI:5581656	M	MP:0002590	increased mean corpuscular volume	Kel<tm1Slee>/Kel<tm1Slee>	B6.129X1-Kel<tm1Slee>	N	23122227
MGI:5581656	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Kel<tm1Slee>/Kel<tm1Slee>	B6.129X1-Kel<tm1Slee>	N	23122227
MGI:5581673	M	MP:0012368	increased erythrocyte magnesium level	Xk<tm1Ariv>/Y	B6.Cg-Xk<tm1Ariv>	N	23122227
MGI:5581673	M	MP:0012372	abnormal erythrocyte ion content	Xk<tm1Ariv>/Y	B6.Cg-Xk<tm1Ariv>	N	23122227
MGI:5581673	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Xk<tm1Ariv>/Y	B6.Cg-Xk<tm1Ariv>	N	23122227
MGI:5581674	M	MP:0011913	abnormal reticulocyte cell number	Kel<tm1Slee>/Kel<tm1Slee>,Xk<tm1Ariv>/Y	B6.Cg-Kel<tm1Slee> Xk<tm1Ariv>	N	23122227
MGI:5581674	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Kel<tm1Slee>/Kel<tm1Slee>,Xk<tm1Ariv>/Y	B6.Cg-Kel<tm1Slee> Xk<tm1Ariv>	N	23122227
MGI:5581674	M	MP:0002590	increased mean corpuscular volume	Kel<tm1Slee>/Kel<tm1Slee>,Xk<tm1Ariv>/Y	B6.Cg-Kel<tm1Slee> Xk<tm1Ariv>	N	23122227
MGI:5581674	M	MP:0012372	abnormal erythrocyte ion content	Kel<tm1Slee>/Kel<tm1Slee>,Xk<tm1Ariv>/Y	B6.Cg-Kel<tm1Slee> Xk<tm1Ariv>	N	23122227
MGI:5581674	M	MP:0012365	increased erythrocyte sodium level	Kel<tm1Slee>/Kel<tm1Slee>,Xk<tm1Ariv>/Y	B6.Cg-Kel<tm1Slee> Xk<tm1Ariv>	N	23122227
MGI:5581714	M	MP:0000598	abnormal liver morphology	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0002941	increased circulating alanine transaminase level	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0020451	decreased sperm progressive motility	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	31664153
MGI:5581714	M	MP:0013279	increased fasting circulating glucose level	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0001922	reduced male fertility	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	31664153
MGI:5581714	M	MP:0014190	abnormal epididymis physiology	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	31664153
MGI:5581714	M	MP:0014465	abnormal sperm mitochondrial morphology	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	31664153
MGI:5581714	M	MP:0002628	hepatic steatosis	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0005416	abnormal circulating protein level	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0003331	increased hepatocellular carcinoma incidence	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0003893	increased hepatocyte proliferation	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0009168	decreased pancreatic islet number	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0009172	small pancreatic islets	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0005293	impaired glucose tolerance	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	F	MP:0005389	reproductive system phenotype	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	Y	24332041
MGI:5581714	M	MP:0001925	male infertility	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0031301	chronic liver inflammation	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0001925	male infertility	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	31664153
MGI:5581714	M	MP:0003887	increased hepatocyte apoptosis	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0009831	abnormal sperm midpiece morphology	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	31664153
MGI:5581714	M	MP:0005578	teratozoospermia	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	31664153
MGI:5581714	M	MP:0003333	liver fibrosis	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0002675	asthenozoospermia	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	31664153
MGI:5581714	M	MP:0009230	abnormal sperm head morphology	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	31664153
MGI:5581714	M	MP:0009355	increased liver triglyceride level	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581714	M	MP:0005331	insulin resistance	Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * C57BL/6	N	24332041
MGI:5581715	M	MP:0005389	reproductive system phenotype	Il6<tm1Kopf>/Il6<+>,Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129S2/SvPas * C57BL/6	Y	24332041
MGI:5581715	M	MP:0003331	increased hepatocellular carcinoma incidence	Il6<tm1Kopf>/Il6<+>,Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129S2/SvPas * C57BL/6	N	24332041
MGI:5581715	M	MP:0005376	homeostasis/metabolism phenotype	Il6<tm1Kopf>/Il6<+>,Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129S2/SvPas * C57BL/6	Y	24332041
MGI:5581716	M	MP:0005376	homeostasis/metabolism phenotype	Il6<tm1Kopf>/Il6<+>,Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129S2/SvPas * BALB/c * C57BL/6	Y	24332041
MGI:5581718	M	MP:0005293	impaired glucose tolerance	Ncoa5<tm1Hxia>/Ncoa5<+>	C.129(B6)-Ncoa5<tm1Hxia>	N	24332041
MGI:5581718	M	MP:0013279	increased fasting circulating glucose level	Ncoa5<tm1Hxia>/Ncoa5<+>	C.129(B6)-Ncoa5<tm1Hxia>	N	24332041
MGI:5581718	M	MP:0003331	increased hepatocellular carcinoma incidence	Ncoa5<tm1Hxia>/Ncoa5<+>	C.129(B6)-Ncoa5<tm1Hxia>	N	24332041
MGI:5581719	F	MP:0009404	centrally nucleated skeletal muscle fibers	Kel<tm1Slee>/Kel<tm1Slee>,Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Kel<tm1Slee> Xk<tm1Ariv>	N	24405768
MGI:5581719	F	MP:0003084	abnormal skeletal muscle fiber morphology	Kel<tm1Slee>/Kel<tm1Slee>,Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Kel<tm1Slee> Xk<tm1Ariv>	N	24405768
MGI:5581719	F	MP:0009403	increased variability of skeletal muscle fiber size	Kel<tm1Slee>/Kel<tm1Slee>,Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Kel<tm1Slee> Xk<tm1Ariv>	N	24405768
MGI:5581719	F	MP:0005369	muscle phenotype	Kel<tm1Slee>/Kel<tm1Slee>,Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Kel<tm1Slee> Xk<tm1Ariv>	Y	24405768
MGI:5581719	F	MP:0011731	decreased myelin sheath thickness	Kel<tm1Slee>/Kel<tm1Slee>,Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Kel<tm1Slee> Xk<tm1Ariv>	N	24405768
MGI:5581719	F	MP:0011730	increased myelin sheath thickness	Kel<tm1Slee>/Kel<tm1Slee>,Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Kel<tm1Slee> Xk<tm1Ariv>	N	24405768
MGI:5581719	F	MP:0010738	abnormal internode morphology	Kel<tm1Slee>/Kel<tm1Slee>,Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Kel<tm1Slee> Xk<tm1Ariv>	N	24405768
MGI:5581719	F	MP:0005404	abnormal axon morphology	Kel<tm1Slee>/Kel<tm1Slee>,Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Kel<tm1Slee> Xk<tm1Ariv>	N	24405768
MGI:5581720	F	MP:0009403	increased variability of skeletal muscle fiber size	Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Xk<tm1Ariv>	N	24405768
MGI:5581720	F	MP:0010738	abnormal internode morphology	Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Xk<tm1Ariv>	N	24405768
MGI:5581720	F	MP:0011730	increased myelin sheath thickness	Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Xk<tm1Ariv>	N	24405768
MGI:5581720	F	MP:0005404	abnormal axon morphology	Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Xk<tm1Ariv>	N	24405768
MGI:5581720	F	MP:0011731	decreased myelin sheath thickness	Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Xk<tm1Ariv>	N	24405768
MGI:5581720	F	MP:0005369	muscle phenotype	Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Xk<tm1Ariv>	Y	24405768
MGI:5581720	F	MP:0009404	centrally nucleated skeletal muscle fibers	Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Xk<tm1Ariv>	N	24405768
MGI:5581720	F	MP:0003084	abnormal skeletal muscle fiber morphology	Xk<tm1Ariv>/Xk<tm1Ariv>	B6.Cg-Xk<tm1Ariv>	N	24405768
MGI:5582744	M	MP:0013209	abnormal motile cilium physiology	Cnbd2<tm1Dwac>/Cnbd2<tm1Dwac>	B6.Cg-Cnbd2<tm1Dwac>	N	24339785
MGI:5582744	M	MP:0002674	abnormal sperm motility	Cnbd2<tm1Dwac>/Cnbd2<tm1Dwac>	B6.Cg-Cnbd2<tm1Dwac>	N	24339785
MGI:5582744	M	MP:0001925	male infertility	Cnbd2<tm1Dwac>/Cnbd2<tm1Dwac>	B6.Cg-Cnbd2<tm1Dwac>	N	24339785
MGI:5582744	M	MP:0001153	small seminiferous tubules	Cnbd2<tm1Dwac>/Cnbd2<tm1Dwac>	B6.Cg-Cnbd2<tm1Dwac>	N	24339785
MGI:5582744	M	MP:0004852	decreased testis weight	Cnbd2<tm1Dwac>/Cnbd2<tm1Dwac>	B6.Cg-Cnbd2<tm1Dwac>	N	24339785
MGI:5582744	M	MP:0001147	small testis	Cnbd2<tm1Dwac>/Cnbd2<tm1Dwac>	B6.Cg-Cnbd2<tm1Dwac>	N	24339785
MGI:5582744	M	MP:0005159	azoospermia	Cnbd2<tm1Dwac>/Cnbd2<tm1Dwac>	B6.Cg-Cnbd2<tm1Dwac>	N	24339785
MGI:5582744	M	MP:0001922	reduced male fertility	Cnbd2<tm1Dwac>/Cnbd2<tm1Dwac>	B6.Cg-Cnbd2<tm1Dwac>	N	24339785
MGI:5582744	M	MP:0004850	abnormal testis weight	Cnbd2<tm1Dwac>/Cnbd2<tm1Dwac>	B6.Cg-Cnbd2<tm1Dwac>	N	24339785
MGI:5582744	M	MP:0001146	abnormal testis morphology	Cnbd2<tm1Dwac>/Cnbd2<tm1Dwac>	B6.Cg-Cnbd2<tm1Dwac>	N	24339785
MGI:5582744	M	MP:0008261	arrest of male meiosis	Cnbd2<tm1Dwac>/Cnbd2<tm1Dwac>	B6.Cg-Cnbd2<tm1Dwac>	N	24339785
MGI:5582744	M	MP:0009831	abnormal sperm midpiece morphology	Cnbd2<tm1Dwac>/Cnbd2<tm1Dwac>	B6.Cg-Cnbd2<tm1Dwac>	N	24339785
MGI:5582777	M	MP:0004499	increased incidence of tumors by chemical induction	Par2<A/J>/?,Poli<tm1.1Lgh>/Poli<+>	involves: A/J * C57BL/6J	N	23955086
MGI:5582778	M	MP:0004499	increased incidence of tumors by chemical induction	Pas17<C57BL/6JBy>/Pas17<C57BL/6JBy>,Poli<tm1.1Lgh>/Poli<+>	involves: C57BL/6J	N	23955086
MGI:5582779	M	MP:0004499	increased incidence of tumors by chemical induction	Pas17<C57BL/6JBy>/Pas17<C57BL/6JBy>,Poli<tm1.1Lgh>/Poli<tm1.1Lgh>	involves: C57BL/6J	N	23955086
MGI:5582779	M	MP:0005621	abnormal cell physiology	Pas17<C57BL/6JBy>/Pas17<C57BL/6JBy>,Poli<tm1.1Lgh>/Poli<tm1.1Lgh>	involves: C57BL/6J	N	23955086
MGI:5582780	M	MP:0004499	increased incidence of tumors by chemical induction	Poli<tm1.1Lgh>/Poli<tm1.1Lgh>,Tg(gptdelta)1Nmi/0	involves: C57BL/6J	N	23955086
MGI:5582780	M	MP:0002006	neoplasm	Poli<tm1.1Lgh>/Poli<tm1.1Lgh>,Tg(gptdelta)1Nmi/0	involves: C57BL/6J	Y	23955086
MGI:5584025	M	MP:0000418	focal hair loss	Mecp2<tm1.1Dhy>/Y	C57BL/6N-Mecp2<tm1.1Dhy>	N	24352790
MGI:5584025	M	MP:0009939	abnormal hippocampus neuron morphology	Mecp2<tm1.1Dhy>/Y	C57BL/6N-Mecp2<tm1.1Dhy>	N	24352790
MGI:5584025	M	MP:0004924	abnormal behavior	Mecp2<tm1.1Dhy>/Y	C57BL/6N-Mecp2<tm1.1Dhy>	N	24352790
MGI:5584025	M	MP:0005378	growth/size/body region phenotype	Mecp2<tm1.1Dhy>/Y	C57BL/6N-Mecp2<tm1.1Dhy>	Y	24352790
MGI:5584025	M	MP:0001212	skin lesions	Mecp2<tm1.1Dhy>/Y	C57BL/6N-Mecp2<tm1.1Dhy>	N	24352790
MGI:5584025	M	MP:0001364	decreased anxiety-related response	Mecp2<tm1.1Dhy>/Y	C57BL/6N-Mecp2<tm1.1Dhy>	N	24352790
MGI:5584025	M	MP:0001406	abnormal gait	Mecp2<tm1.1Dhy>/Y	C57BL/6N-Mecp2<tm1.1Dhy>	N	24352790
MGI:5584025	M	MP:0001441	increased grooming behavior	Mecp2<tm1.1Dhy>/Y	C57BL/6N-Mecp2<tm1.1Dhy>	N	24352790
MGI:5584025	M	MP:0002064	seizures	Mecp2<tm1.1Dhy>/Y	C57BL/6N-Mecp2<tm1.1Dhy>	N	24352790
MGI:5584025	M	MP:0002083	premature death	Mecp2<tm1.1Dhy>/Y	C57BL/6N-Mecp2<tm1.1Dhy>	N	24352790
MGI:5584025	M	MP:0001360	abnormal social investigation	Mecp2<tm1.1Dhy>/Y	C57BL/6N-Mecp2<tm1.1Dhy>	N	24352790
MGI:5584026	F	MP:0004924	abnormal behavior	Mecp2<tm1.1Dhy>/Mecp2<+>	C57BL/6N-Mecp2<tm1.1Dhy>	N	24352790
MGI:5584026	F	MP:0001513	limb grasping	Mecp2<tm1.1Dhy>/Mecp2<+>	C57BL/6N-Mecp2<tm1.1Dhy>	N	24352790
MGI:5584026	F	MP:0005378	growth/size/body region phenotype	Mecp2<tm1.1Dhy>/Mecp2<+>	C57BL/6N-Mecp2<tm1.1Dhy>	Y	24352790
MGI:5584140	F	MP:0002169	no abnormal phenotype detected	Etn3<tm1Jwi>/Etn3<+>	involves: C57BL/6	N	24339789
MGI:5584141	F	MP:0006279	abnormal limb development	Etn3<tm1.1Jwi>/Etn3<+>	involves: C57BL/6	N	24339789
MGI:5584141	F	MP:0002113	abnormal skeleton development	Etn3<tm1.1Jwi>/Etn3<+>	involves: C57BL/6	N	24339789
MGI:5584142	F	MP:0002113	abnormal skeleton development	Etn3<tm1.1Jwi>/Etn3<+>	involves: C57BL/6 * DBA/2	N	24339789
MGI:5584142	F	MP:0006279	abnormal limb development	Etn3<tm1.1Jwi>/Etn3<+>	involves: C57BL/6 * DBA/2	N	24339789
MGI:5584143	F	MP:0002113	abnormal skeleton development	Etn3<tm1.1Jwi>/Etn3<+>	involves: C57BL/6 * FVB	N	24339789
MGI:5584143	F	MP:0006279	abnormal limb development	Etn3<tm1.1Jwi>/Etn3<+>	involves: C57BL/6 * FVB	N	24339789
MGI:5584144	F	MP:0002169	no abnormal phenotype detected	Etn3<tm2Jwi>/Etn3<+>	involves: C57BL/6J	N	24339789
MGI:5584145	F	MP:0002113	abnormal skeleton development	Etn3<tm2.1Jwi>/Etn3<+>	involves: C57BL/6J	N	24339789
MGI:5584145	F	MP:0006279	abnormal limb development	Etn3<tm2.1Jwi>/Etn3<+>	involves: C57BL/6J	N	24339789
MGI:5584146	F	MP:0006279	abnormal limb development	Etn3<tm2.1Jwi>/Etn3<+>	involves: C57BL/6 * C57BL/6J * DBA/2	N	24339789
MGI:5584146	F	MP:0002113	abnormal skeleton development	Etn3<tm2.1Jwi>/Etn3<+>	involves: C57BL/6 * C57BL/6J * DBA/2	N	24339789
MGI:5584147	F	MP:0002113	abnormal skeleton development	Etn3<tm2.1Jwi>/Etn3<+>	involves: C57BL/6J * FVB	N	24339789
MGI:5584147	F	MP:0006279	abnormal limb development	Etn3<tm2.1Jwi>/Etn3<+>	involves: C57BL/6J * FVB	N	24339789
MGI:5584173	M	MP:0001953	respiratory failure	Del(XNxf2-Nxf3)1Jw/Y	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5584173	M	MP:0001176	abnormal lung development	Del(XNxf2-Nxf3)1Jw/Y	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5584173	M	MP:0011087	neonatal lethality, complete penetrance	Del(XNxf2-Nxf3)1Jw/Y	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5584173	M	MP:0011142	abnormal lung-associated mesenchyme development	Del(XNxf2-Nxf3)1Jw/Y	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5584173	M	MP:0021213	complete cleft palate	Del(XNxf2-Nxf3)1Jw/Y	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5584173	M	MP:0001178	pulmonary hypoplasia	Del(XNxf2-Nxf3)1Jw/Y	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5584179	M	MP:0000111	cleft palate	Del(XArmcx5-Nxf3)3Jw/Y	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	24569167
MGI:5584179	M	MP:0011087	neonatal lethality, complete penetrance	Del(XArmcx5-Nxf3)3Jw/Y	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	24569167
MGI:5584179	M	MP:0001953	respiratory failure	Del(XArmcx5-Nxf3)3Jw/Y	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	24569167
MGI:5584182	F	MP:0009358	environmentally induced seizures	Del(XArmcx5-Nxf3)3Jw/+	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	24569167
MGI:5584182	F	MP:0011086	postnatal lethality, incomplete penetrance	Del(XArmcx5-Nxf3)3Jw/+	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	24569167
MGI:5584182	F	MP:0001732	postnatal growth retardation	Del(XArmcx5-Nxf3)3Jw/+	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	24569167
MGI:5584182	F	MP:0000111	cleft palate	Del(XArmcx5-Nxf3)3Jw/+	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	24569167
MGI:5584183	M	MP:0002169	no abnormal phenotype detected	Del(XNxf2-Tmsb15a)2Jw/Y	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5584184	F	MP:0002169	no abnormal phenotype detected	Del(XNxf2-Tmsb15a)2Jw/Del(XNxf2-Tmsb15a)2Jw	involves: 129S4/SvJae * C57BL/6 * FVB	N	24569167
MGI:5584309	F	MP:0008779	abnormal maternal behavior	Gng8<tm1(tTA)Rtir>/Gng8<tm1(tTA)Rtir>	FVB.129-Gng8<tm1(tTA)Rtir>	N	23836683
MGI:5584309	M	MP:0001360	abnormal social investigation	Gng8<tm1(tTA)Rtir>/Gng8<tm1(tTA)Rtir>	FVB.129-Gng8<tm1(tTA)Rtir>	N	23836683
MGI:5584312	M	MP:0031508	abnormal vascular smooth muscle cell proliferation	Gja1<tm3.1Clo>/Gja1<tm3.1Clo>	B6.Cg-Gja1<tm1.1Clo>	N	22652908
MGI:5584312	M	MP:0004883	abnormal vascular wound healing	Gja1<tm3.1Clo>/Gja1<tm3.1Clo>	B6.Cg-Gja1<tm1.1Clo>	N	22652908
MGI:5584315	F	MP:0002777	absent ovarian follicles	Mad2l2<repro22>/Mad2l2<repro22>	C3.B6(Cg)-Mad2l2<repro22>	N	24356953
MGI:5584315	M	MP:0001925	male infertility	Mad2l2<repro22>/Mad2l2<repro22>	C3.B6(Cg)-Mad2l2<repro22>	N	24356953
MGI:5584315	F	MP:0001127	small ovary	Mad2l2<repro22>/Mad2l2<repro22>	C3.B6(Cg)-Mad2l2<repro22>	N	24356953
MGI:5584315	F	MP:0001926	female infertility	Mad2l2<repro22>/Mad2l2<repro22>	C3.B6(Cg)-Mad2l2<repro22>	N	24356953
MGI:5584315	M	MP:0001147	small testis	Mad2l2<repro22>/Mad2l2<repro22>	C3.B6(Cg)-Mad2l2<repro22>	N	24356953
MGI:5585410	M	MP:0001516	abnormal motor coordination/balance	Ppt1<tm1.1Dprc>/Ppt1<tm1.1Dprc>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6	N	25205113
MGI:5585410	M	MP:0001417	decreased exploration in new environment	Ppt1<tm1.1Dprc>/Ppt1<tm1.1Dprc>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6	N	25205113
MGI:5585410	M	MP:0001405	impaired coordination	Ppt1<tm1.1Dprc>/Ppt1<tm1.1Dprc>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6	N	25205113
MGI:5585440	M	MP:0005397	hematopoietic system phenotype	Cd40lg<tm1Parl>/Y,Tg(Cd4-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	Y	24030045
MGI:5585440	M	MP:0005376	homeostasis/metabolism phenotype	Cd40lg<tm1Parl>/Y,Tg(Cd4-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	Y	24030045
MGI:5585440	M	MP:0005387	immune system phenotype	Cd40lg<tm1Parl>/Y,Tg(Cd4-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	Y	24030045
MGI:5585441	F	MP:0005387	immune system phenotype	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Tg(Cd4-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	Y	24030045
MGI:5585441	F	MP:0005376	homeostasis/metabolism phenotype	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Tg(Cd4-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	Y	24030045
MGI:5585441	F	MP:0005397	hematopoietic system phenotype	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Tg(Cd4-cre)1Cwi/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	Y	24030045
MGI:5585442	F	MP:0005376	homeostasis/metabolism phenotype	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca	Y	24030045
MGI:5585442	F	MP:0005397	hematopoietic system phenotype	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca	Y	24030045
MGI:5585442	F	MP:0008499	increased IgG1 level	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca	N	24030045
MGI:5585442	F	MP:0001806	decreased IgM level	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca	N	24030045
MGI:5585442	F	MP:0003179	thrombocytopenia	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca	N	24030045
MGI:5585443	M	MP:0005397	hematopoietic system phenotype	Cd40lg<tm1Parl>/Y,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca	Y	24030045
MGI:5585443	M	MP:0001806	decreased IgM level	Cd40lg<tm1Parl>/Y,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca	N	24030045
MGI:5585443	M	MP:0008499	increased IgG1 level	Cd40lg<tm1Parl>/Y,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca	N	24030045
MGI:5585443	M	MP:0003179	thrombocytopenia	Cd40lg<tm1Parl>/Y,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca	N	24030045
MGI:5585443	M	MP:0005376	homeostasis/metabolism phenotype	Cd40lg<tm1Parl>/Y,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca	Y	24030045
MGI:5585444	M	MP:0008495	decreased IgG1 level	Cd40lg<tm1Parl>/Y,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	N	24030045
MGI:5585444	M	MP:0005397	hematopoietic system phenotype	Cd40lg<tm1Parl>/Y,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	Y	24030045
MGI:5585444	M	MP:0008496	decreased IgG2a level	Cd40lg<tm1Parl>/Y,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	N	24030045
MGI:5585444	M	MP:0001807	decreased IgA level	Cd40lg<tm1Parl>/Y,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	N	24030045
MGI:5585444	M	MP:0008498	decreased IgG3 level	Cd40lg<tm1Parl>/Y,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	N	24030045
MGI:5585444	M	MP:0001806	decreased IgM level	Cd40lg<tm1Parl>/Y,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	N	24030045
MGI:5585444	M	MP:0005376	homeostasis/metabolism phenotype	Cd40lg<tm1Parl>/Y,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	Y	24030045
MGI:5585446	F	MP:0005376	homeostasis/metabolism phenotype	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	Y	24030045
MGI:5585446	F	MP:0005397	hematopoietic system phenotype	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	Y	24030045
MGI:5585446	F	MP:0001807	decreased IgA level	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	N	24030045
MGI:5585446	F	MP:0008495	decreased IgG1 level	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	N	24030045
MGI:5585446	F	MP:0001806	decreased IgM level	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	N	24030045
MGI:5585446	F	MP:0008498	decreased IgG3 level	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	N	24030045
MGI:5585446	F	MP:0008496	decreased IgG2a level	Cd40lg<tm1Parl>/Cd40lg<tm1Parl>,Tg(Tek-cre)1Ywa/0	involves: 129 * C57BL/6 * CD-1 * SJL	N	24030045
MGI:5586541	F	MP:0000418	focal hair loss	Xlhl/Xlhl<+>	B6.Cg-Xlhl/GrsrJ	N	MGI:5586539
MGI:5586541	F	MP:0000377	abnormal hair follicle morphology	Xlhl/Xlhl<+>	B6.Cg-Xlhl/GrsrJ	N	MGI:5586539
MGI:5586542	M	MP:0000377	abnormal hair follicle morphology	Xlhl/Y	B6.Cg-Xlhl/GrsrJ	N	MGI:5586539
MGI:5586542	M	MP:0000416	sparse hair	Xlhl/Y	B6.Cg-Xlhl/GrsrJ	N	MGI:5586539
MGI:5586543	F	MP:0000416	sparse hair	Xlhl/Xlhl	B6.Cg-Xlhl/GrsrJ	N	MGI:5586539
MGI:5586690	M	MP:0008515	thin retina outer nuclear layer	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0001891	hydrocephaly	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0005241	abnormal retina ganglion layer morphology	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0002864	abnormal ocular fundus morphology	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0008852	retina neovascularization	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0003728	abnormal retina photoreceptor layer morphology	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0001325	abnormal retina morphology	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0010236	abnormal retina outer limiting membrane morphology	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0003727	abnormal retina layer morphology	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0014336	short retina rod cell outer segment	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0003731	abnormal retina outer nuclear layer morphology	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0012029	abnormal electroretinogram waveform feature	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0005201	abnormal retina pigment epithelium morphology	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0008449	abnormal retina cone cell outer segment morphology	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0012676	dilated brain ventricle	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0005547	abnormal Muller cell morphology	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0012143	decreased a-wave amplitude	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0031606	increased susceptibility to age-related retinal degeneration	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586690	M	MP:0003732	abnormal retina outer plexiform layer morphology	Crb2<tm1.1Wij>/Crb2<tm1.1Wij>,Tg(Crx-cre)1Tfur/0	involves: 129P2/OlaHsd * C57BL/6J	N	24493795
MGI:5586716	M	MP:0000604	amyloidosis	Cst3<tm1(CST3*L68Q)Cnw>/Cst3<+>	involves: 129P2/OlaHsd * C57BL/6	N	24500719
MGI:5586716	M	MP:0001922	reduced male fertility	Cst3<tm1(CST3*L68Q)Cnw>/Cst3<+>	involves: 129P2/OlaHsd * C57BL/6	N	24500719
MGI:5586716	M	MP:0002675	asthenozoospermia	Cst3<tm1(CST3*L68Q)Cnw>/Cst3<+>	involves: 129P2/OlaHsd * C57BL/6	N	24500719
MGI:5586716	M	MP:0030978	impaired binding of sperm to zona pellucida	Cst3<tm1(CST3*L68Q)Cnw>/Cst3<+>	involves: 129P2/OlaHsd * C57BL/6	N	24500719
MGI:5586716	M	MP:0006362	abnormal male germ cell morphology	Cst3<tm1(CST3*L68Q)Cnw>/Cst3<+>	involves: 129P2/OlaHsd * C57BL/6	N	24500719
MGI:5586724	M	MP:0009289	decreased epididymal fat pad weight	Gt(ROSA)26Sor<tm1(Sirt1)Ktm>/Gt(ROSA)26Sor<+>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * C57BL/6J * FVB/N	N	24374551
MGI:5586724	M	MP:0004889	increased energy expenditure	Gt(ROSA)26Sor<tm1(Sirt1)Ktm>/Gt(ROSA)26Sor<+>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * C57BL/6J * FVB/N	N	24374551
MGI:5586724	M	MP:0003213	decreased susceptibility to age related obesity	Gt(ROSA)26Sor<tm1(Sirt1)Ktm>/Gt(ROSA)26Sor<+>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * C57BL/6J * FVB/N	N	24374551
MGI:5586724	M	MP:0010025	decreased total body fat amount	Gt(ROSA)26Sor<tm1(Sirt1)Ktm>/Gt(ROSA)26Sor<+>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * C57BL/6J * FVB/N	N	24374551
MGI:5586724	M	MP:0005289	increased oxygen consumption	Gt(ROSA)26Sor<tm1(Sirt1)Ktm>/Gt(ROSA)26Sor<+>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * C57BL/6J * FVB/N	N	24374551
MGI:5586724	M	MP:0021023	increased adipose tissue noradrenaline turnover	Gt(ROSA)26Sor<tm1(Sirt1)Ktm>/Gt(ROSA)26Sor<+>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * C57BL/6J * FVB/N	N	24374551
MGI:5586724	M	MP:0001402	decreased locomotor activity	Gt(ROSA)26Sor<tm1(Sirt1)Ktm>/Gt(ROSA)26Sor<+>,Tg(Pomc1-cre)16Lowl/0	involves: 129 * C57BL/6J * FVB/N	N	24374551
MGI:5586725	M	MP:0011940	decreased food intake	Gt(ROSA)26Sor<tm1(Sirt1)Ktm>/Gt(ROSA)26Sor<+>,Tg(Agrp-cre)1Gsb/0	involves: 129 * C57BL/6J * FVB/N	N	24374551
MGI:5586725	F	MP:0011939	increased food intake	Gt(ROSA)26Sor<tm1(Sirt1)Ktm>/Gt(ROSA)26Sor<+>,Tg(Agrp-cre)1Gsb/0	involves: 129 * C57BL/6J * FVB/N	N	24374551
MGI:5586725	M	MP:0003213	decreased susceptibility to age related obesity	Gt(ROSA)26Sor<tm1(Sirt1)Ktm>/Gt(ROSA)26Sor<+>,Tg(Agrp-cre)1Gsb/0	involves: 129 * C57BL/6J * FVB/N	N	24374551
MGI:5586725	F	MP:0001260	increased body weight	Gt(ROSA)26Sor<tm1(Sirt1)Ktm>/Gt(ROSA)26Sor<+>,Tg(Agrp-cre)1Gsb/0	involves: 129 * C57BL/6J * FVB/N	N	24374551
MGI:5587824	M	MP:0005159	azoospermia	Hormad1<tm1Kura>/Hormad1<tm1Kura>	either: B6.Cg-Hormad1<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	22530760
MGI:5587824	M	MP:0005169	abnormal male meiosis	Hormad1<tm1Kura>/Hormad1<tm1Kura>	either: B6.Cg-Hormad1<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	22530760
MGI:5587824	M	MP:0008261	arrest of male meiosis	Hormad1<tm1Kura>/Hormad1<tm1Kura>	either: B6.Cg-Hormad1<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	22530760
MGI:5587824	M	MP:0008058	abnormal DNA repair	Hormad1<tm1Kura>/Hormad1<tm1Kura>	either: B6.Cg-Hormad1<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	22530760
MGI:5587824	F	MP:0005168	abnormal female meiosis	Hormad1<tm1Kura>/Hormad1<tm1Kura>	either: B6.Cg-Hormad1<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	22530760
MGI:5587824	M	MP:0008280	abnormal male germ cell apoptosis	Hormad1<tm1Kura>/Hormad1<tm1Kura>	either: B6.Cg-Hormad1<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	22530760
MGI:5587824	M	MP:0001925	male infertility	Hormad1<tm1Kura>/Hormad1<tm1Kura>	either: B6.Cg-Hormad1<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	22530760
MGI:5587824	F	MP:0004024	aneuploidy	Hormad1<tm1Kura>/Hormad1<tm1Kura>	either: B6.Cg-Hormad1<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	22530760
MGI:5587824	M	MP:0004852	decreased testis weight	Hormad1<tm1Kura>/Hormad1<tm1Kura>	either: B6.Cg-Hormad1<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	22530760
MGI:5587824	F	MP:0003718	maternal effect	Hormad1<tm1Kura>/Hormad1<tm1Kura>	either: B6.Cg-Hormad1<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	N	22530760
MGI:5587824	F	MP:0005389	reproductive system phenotype	Hormad1<tm1Kura>/Hormad1<tm1Kura>	either: B6.Cg-Hormad1<tm1Kura> or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	Y	22530760
MGI:5587825	F	MP:0005389	reproductive system phenotype	Hormad1<tm1Kura>/Hormad1<tm1Kura>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj	Y	22530760
MGI:5587825	F	MP:0005168	abnormal female meiosis	Hormad1<tm1Kura>/Hormad1<tm1Kura>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj	N	22530760
MGI:5587825	M	MP:0005169	abnormal male meiosis	Hormad1<tm1Kura>/Hormad1<tm1Kura>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj	N	22530760
MGI:5587825	M	MP:0008280	abnormal male germ cell apoptosis	Hormad1<tm1Kura>/Hormad1<tm1Kura>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj	N	22530760
MGI:5588023	M	MP:0002169	no abnormal phenotype detected	Hmgn5<tm1.1Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	MGI:5427973
MGI:5588102	F	MP:0001958	emphysema	Hmgn5<tm1.2Mbus>/Hmgn5<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588102	F	MP:0002311	abnormal inspiratory capacity	Hmgn5<tm1.2Mbus>/Hmgn5<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588102	F	MP:0005291	abnormal glucose tolerance	Hmgn5<tm1.2Mbus>/Hmgn5<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588102	F	MP:0001586	abnormal erythrocyte cell number	Hmgn5<tm1.2Mbus>/Hmgn5<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588102	F	MP:0008078	increased CD8-positive, alpha-beta T cell number	Hmgn5<tm1.2Mbus>/Hmgn5<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588102	F	MP:0002495	increased IgA level	Hmgn5<tm1.2Mbus>/Hmgn5<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588102	F	MP:0002492	decreased IgE level	Hmgn5<tm1.2Mbus>/Hmgn5<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588102	F	MP:0009142	decreased prepulse inhibition	Hmgn5<tm1.2Mbus>/Hmgn5<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588102	F	MP:0001943	abnormal respiration	Hmgn5<tm1.2Mbus>/Hmgn5<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588102	F	MP:0002297	abnormal forced expiratory flow rates	Hmgn5<tm1.2Mbus>/Hmgn5<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588102	F	MP:0002304	abnormal total lung capacity	Hmgn5<tm1.2Mbus>/Hmgn5<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588102	F	MP:0002314	abnormal respiratory mechanics	Hmgn5<tm1.2Mbus>/Hmgn5<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588102	F	MP:0000334	decreased granulocyte number	Hmgn5<tm1.2Mbus>/Hmgn5<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588103	F	MP:0002665	decreased circulating corticosterone level	Hmgn3<tm1.2Mbus>/Hmgn3<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588103	M	MP:0002781	increased circulating testosterone level	Hmgn3<tm1.2Mbus>/Hmgn3<tm1.2Mbus>	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588107	M	MP:0005291	abnormal glucose tolerance	Hmgn5<tm1.2Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588107	M	MP:0002314	abnormal respiratory mechanics	Hmgn5<tm1.2Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588107	M	MP:0002495	increased IgA level	Hmgn5<tm1.2Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588107	M	MP:0009142	decreased prepulse inhibition	Hmgn5<tm1.2Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588107	M	MP:0001943	abnormal respiration	Hmgn5<tm1.2Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588107	M	MP:0001958	emphysema	Hmgn5<tm1.2Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588107	M	MP:0002297	abnormal forced expiratory flow rates	Hmgn5<tm1.2Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588107	M	MP:0002304	abnormal total lung capacity	Hmgn5<tm1.2Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588107	M	MP:0002492	decreased IgE level	Hmgn5<tm1.2Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588107	M	MP:0002311	abnormal inspiratory capacity	Hmgn5<tm1.2Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588107	M	MP:0008078	increased CD8-positive, alpha-beta T cell number	Hmgn5<tm1.2Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588107	M	MP:0000334	decreased granulocyte number	Hmgn5<tm1.2Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588107	M	MP:0001586	abnormal erythrocyte cell number	Hmgn5<tm1.2Mbus>/Y	involves: 129S4/SvJae * C57BL/6J	N	23620591
MGI:5588371	M	MP:0003998	decreased thermal nociceptive threshold	Ntrk1<tm2.1Tes>/Ntrk1<tm2.1Tes>	B6.129S1(Cg)-Ntrk1<tm2.1Tes>	N	24623787
MGI:5588371	M	MP:0003663	abnormal thermosensation	Ntrk1<tm2.1Tes>/Ntrk1<tm2.1Tes>	B6.129S1(Cg)-Ntrk1<tm2.1Tes>	N	24623787
MGI:5588371	M	MP:0002736	abnormal nociception after inflammation	Ntrk1<tm2.1Tes>/Ntrk1<tm2.1Tes>	B6.129S1(Cg)-Ntrk1<tm2.1Tes>	N	24623787
MGI:5588690	M	MP:0005659	decreased susceptibility to diet-induced obesity	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0010025	decreased total body fat amount	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0001780	decreased brown adipose tissue amount	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0002727	decreased circulating insulin level	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0009133	decreased white fat cell size	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0006319	abnormal epididymal fat pad morphology	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0008844	decreased subcutaneous adipose tissue amount	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0003402	decreased liver weight	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0000598	abnormal liver morphology	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0005292	improved glucose tolerance	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0009356	decreased liver triglyceride level	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0008554	decreased circulating tumor necrosis factor level	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0005376	homeostasis/metabolism phenotype	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	Y	24675075
MGI:5588690	M	MP:0002891	increased insulin sensitivity	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0010360	decreased liver free fatty acids level	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588690	M	MP:0009136	decreased brown fat cell size	Sra1<tm1a(EUCOMM)Hmgu>/Sra1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	24675075
MGI:5588706	M	MP:0031602	white adipose tissue inflammation	Ddit3<tm2.1Dron>/Ddit3<tm2.1Dron>	B6.129S(Cg)-Ddit3<tm2.1Dron>/J	N	24662293
MGI:5588706	M	MP:0010024	increased total body fat amount	Ddit3<tm2.1Dron>/Ddit3<tm2.1Dron>	B6.129S(Cg)-Ddit3<tm2.1Dron>/J	N	24662293
MGI:5588706	M	MP:0005658	increased susceptibility to diet-induced obesity	Ddit3<tm2.1Dron>/Ddit3<tm2.1Dron>	B6.129S(Cg)-Ddit3<tm2.1Dron>/J	N	24662293
MGI:5588706	M	MP:0002628	hepatic steatosis	Ddit3<tm2.1Dron>/Ddit3<tm2.1Dron>	B6.129S(Cg)-Ddit3<tm2.1Dron>/J	N	24662293
MGI:5588706	M	MP:0004890	decreased energy expenditure	Ddit3<tm2.1Dron>/Ddit3<tm2.1Dron>	B6.129S(Cg)-Ddit3<tm2.1Dron>/J	N	24662293
MGI:5588706	M	MP:0001402	decreased locomotor activity	Ddit3<tm2.1Dron>/Ddit3<tm2.1Dron>	B6.129S(Cg)-Ddit3<tm2.1Dron>/J	N	24662293
MGI:5588706	M	MP:0005331	insulin resistance	Ddit3<tm2.1Dron>/Ddit3<tm2.1Dron>	B6.129S(Cg)-Ddit3<tm2.1Dron>/J	N	24662293
MGI:5588706	M	MP:0008037	abnormal T cell morphology	Ddit3<tm2.1Dron>/Ddit3<tm2.1Dron>	B6.129S(Cg)-Ddit3<tm2.1Dron>/J	N	24662293
MGI:5588706	M	MP:0003982	increased cholesterol level	Ddit3<tm2.1Dron>/Ddit3<tm2.1Dron>	B6.129S(Cg)-Ddit3<tm2.1Dron>/J	N	24662293
MGI:5588706	M	MP:0005293	impaired glucose tolerance	Ddit3<tm2.1Dron>/Ddit3<tm2.1Dron>	B6.129S(Cg)-Ddit3<tm2.1Dron>/J	N	24662293
MGI:5588805	M	MP:0001745	increased circulating corticosterone level	htd/htd	C3H/HeJ-htd/J	N	MGI:1932049
MGI:5603758	F	MP:0006271	abnormal involution of the mammary gland	Tg(MMTV-Akt1)1173Stma/0	involves: FVB/N	N	11376107
MGI:5604421	M	MP:0001925	male infertility	Kcnn2<bc-6J>/Kcnn2<bc-6J>	C57BL/6J-Kcnn2<bc-6J>/GrsrJ	N	MGI:5604381
MGI:5604725	M	MP:0009454	impaired contextual conditioning behavior	Mapt<tm1(EGFP)Klt>/Mapt<tm1(EGFP)Klt>	B6.129S4-Mapt<tm1(EGFP)Klt>	N	24913895
MGI:5604725	M	MP:0009456	impaired cued conditioning behavior	Mapt<tm1(EGFP)Klt>/Mapt<tm1(EGFP)Klt>	B6.129S4-Mapt<tm1(EGFP)Klt>	N	24913895
MGI:5604725	M	MP:0002804	abnormal motor learning	Mapt<tm1(EGFP)Klt>/Mapt<tm1(EGFP)Klt>	B6.129S4-Mapt<tm1(EGFP)Klt>	N	24913895
MGI:5604725	M	MP:0001473	reduced long-term potentiation	Mapt<tm1(EGFP)Klt>/Mapt<tm1(EGFP)Klt>	B6.129S4-Mapt<tm1(EGFP)Klt>	N	24913895
MGI:5604725	M	MP:0012306	enhanced spatial learning	Mapt<tm1(EGFP)Klt>/Mapt<tm1(EGFP)Klt>	B6.129S4-Mapt<tm1(EGFP)Klt>	N	24913895
MGI:5604728	F	MP:0004896	abnormal endometrium morphology	Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Cdh16-cre)91Igr/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N * ICR	N	22678923
MGI:5604728	F	MP:0004868	increased endometrial carcinoma incidence	Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Cdh16-cre)91Igr/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N * ICR	N	24930886
MGI:5604728	M	MP:0002661	abnormal corpus epididymis morphology	Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Cdh16-cre)91Igr/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N * ICR	N	22678923
MGI:5604728	F	MP:0004868	increased endometrial carcinoma incidence	Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Cdh16-cre)91Igr/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N * ICR	N	22678923
MGI:5604773	F	MP:0031422	failure of superovulation	Esr2<tm1.1Ksk>/Esr2<tm1.1Ksk>	involves: C57BL/6	N	23580569
MGI:5604773	F	MP:0001923	reduced female fertility	Esr2<tm1.1Ksk>/Esr2<tm1.1Ksk>	involves: C57BL/6	N	23580569
MGI:5604773	F	MP:0003355	decreased ovulation rate	Esr2<tm1.1Ksk>/Esr2<tm1.1Ksk>	involves: C57BL/6	N	23580569
MGI:5604775	M	MP:0001147	small testis	Pepd<dal>/Pepd<dal>	involves: C3H/HeJ * CBA/J	N	18821597
MGI:5604775	M	MP:0002216	abnormal seminiferous tubule morphology	Pepd<dal>/Pepd<dal>	involves: C3H/HeJ * CBA/J	N	18821597
MGI:5604775	M	MP:0001146	abnormal testis morphology	Pepd<dal>/Pepd<dal>	involves: C3H/HeJ * CBA/J	N	18821597
MGI:5604775	M	MP:0011416	abnormal testis interstitial tissue morphology	Pepd<dal>/Pepd<dal>	involves: C3H/HeJ * CBA/J	N	18821597
MGI:5604775	M	MP:0002780	decreased circulating testosterone level	Pepd<dal>/Pepd<dal>	involves: C3H/HeJ * CBA/J	N	18821597
MGI:5604880	M	MP:0001922	reduced male fertility	Tg(MMTV-Erbb2)10Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604880	M	MP:0002997	enlarged seminal vesicle	Tg(MMTV-Erbb2)10Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604880	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-Erbb2)10Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604880	F	MP:0008476	increased spleen red pulp amount	Tg(MMTV-Erbb2)10Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604880	M	MP:0004931	enlarged epididymis	Tg(MMTV-Erbb2)10Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604880	F	MP:0000691	enlarged spleen	Tg(MMTV-Erbb2)10Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604880	F	MP:0010318	increased salivary gland tumor incidence	Tg(MMTV-Erbb2)10Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604887	M	MP:0001922	reduced male fertility	Tg(MMTV-Erbb2)9Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604887	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-Erbb2)9Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604887	F	MP:0000691	enlarged spleen	Tg(MMTV-Erbb2)9Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604887	F	MP:0008476	increased spleen red pulp amount	Tg(MMTV-Erbb2)9Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604887	M	MP:0002997	enlarged seminal vesicle	Tg(MMTV-Erbb2)9Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604887	M	MP:0004931	enlarged epididymis	Tg(MMTV-Erbb2)9Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604891	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-Erbb2)12Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604891	M	MP:0002997	enlarged seminal vesicle	Tg(MMTV-Erbb2)12Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604891	M	MP:0010318	increased salivary gland tumor incidence	Tg(MMTV-Erbb2)12Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604891	F	MP:0000691	enlarged spleen	Tg(MMTV-Erbb2)12Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604891	M	MP:0001922	reduced male fertility	Tg(MMTV-Erbb2)12Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604891	F	MP:0008476	increased spleen red pulp amount	Tg(MMTV-Erbb2)12Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604891	M	MP:0004931	enlarged epididymis	Tg(MMTV-Erbb2)12Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604892	F	MP:0000691	enlarged spleen	Tg(MMTV-Erbb2)17Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604892	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-Erbb2)17Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604892	F	MP:0008476	increased spleen red pulp amount	Tg(MMTV-Erbb2)17Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604892	M	MP:0001922	reduced male fertility	Tg(MMTV-Erbb2)17Pjo/0	involves: BALB/c * C3H * C57BL/6	N	2567634
MGI:5604918	M	MP:0005169	abnormal male meiosis	Cyp26b1<tm1Dcp>/Cyp26b1<tm1Dcp>	involves: 129S4/SvJae * C57BL/6	N	25102060
MGI:5605474	M	MP:0005166	decreased susceptibility to injury	Hprt1<tm1(ACTB-Opa1)Lsc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	24055366
MGI:5605474	M	MP:0011635	abnormal mitochondrial crista morphology	Hprt1<tm1(ACTB-Opa1)Lsc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	24055366
MGI:5605474	M	MP:0006036	abnormal mitochondrial physiology	Hprt1<tm1(ACTB-Opa1)Lsc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	24055366
MGI:5605474	M	MP:0005378	growth/size/body region phenotype	Hprt1<tm1(ACTB-Opa1)Lsc>/Y	involves: 129 * C57BL/6 * C57BL/6J	Y	24055366
MGI:5605556	F	MP:0005431	decreased oocyte number	Peg3<tm1a(EUCOMM)Hmgu>/Peg3<+>	involves: C57BL/6N	N	24391757
MGI:5605556	M	MP:0001147	small testis	Peg3<tm1a(EUCOMM)Hmgu>/Peg3<+>	involves: C57BL/6N	N	24391757
MGI:5605562	F	MP:0003797	abnormal compact bone morphology	Naca<tm2Star>/Naca<+>,Txlng<tm1.2Star>/Txlng<+>	involves: 129S1/Sv * 129X1/SvJ	N	24440290
MGI:5605563	F	MP:0002169	no abnormal phenotype detected	Naca<tm2Star>/Naca<+>	Not Specified	N	24440290
MGI:5605670	M	MP:0001146	abnormal testis morphology	Atrn<mg-3J>/Atrn<+>,Pepd<dal>/Pepd<dal>	involves: C3H/HeJ * C3HeB/FeJ * CBA/J	N	18821597
MGI:5605679	M	MP:0001146	abnormal testis morphology	Atrn<mg-3J>/Atrn<+>,Pepd<dal>/Pepd<+>	involves: C3H/HeJ * C3HeB/FeJ * CBA/J	N	18821597
MGI:5605680	M	MP:0001146	abnormal testis morphology	Pepd<dal>/Pepd<dal>	involves: C3H/HeJ * C3HeB/FeJ * CBA/J	N	18821597
MGI:5605683	M	MP:0001146	abnormal testis morphology	Pepd<dal>/Pepd<dal>,Tg(ACTB-Atrnl1)B4Tmg/0	involves: C57BL/6 * CBA/J * DBA/J	N	18821597
MGI:5605732	F	MP:0002169	no abnormal phenotype detected	Txlng<tm1.2Star>/Txlng<+>	involves: 129S1/Sv * 129X1/SvJ	N	24440290
MGI:5606182	M	MP:0005608	cardiac interstitial fibrosis	Nek6<tm1Dgen>/Nek6<tm1Dgen>	involves: 129S1/Sv * 129X1/SvJ	N	24763737
MGI:5606182	M	MP:0002833	increased heart weight	Nek6<tm1Dgen>/Nek6<tm1Dgen>	involves: 129S1/Sv * 129X1/SvJ	N	24763737
MGI:5606182	M	MP:0001625	cardiac hypertrophy	Nek6<tm1Dgen>/Nek6<tm1Dgen>	involves: 129S1/Sv * 129X1/SvJ	N	24763737
MGI:5606182	M	MP:0031633	decreased heart left ventricle muscle contractility	Nek6<tm1Dgen>/Nek6<tm1Dgen>	involves: 129S1/Sv * 129X1/SvJ	N	24763737
MGI:5606182	M	MP:0004485	increased response of heart to induced stress	Nek6<tm1Dgen>/Nek6<tm1Dgen>	involves: 129S1/Sv * 129X1/SvJ	N	24763737
MGI:5606182	M	MP:0004564	increased myocardial fiber size	Nek6<tm1Dgen>/Nek6<tm1Dgen>	involves: 129S1/Sv * 129X1/SvJ	N	24763737
MGI:5606182	M	MP:0005630	increased lung weight	Nek6<tm1Dgen>/Nek6<tm1Dgen>	involves: 129S1/Sv * 129X1/SvJ	N	24763737
MGI:5606186	F	MP:0002169	no abnormal phenotype detected	Diaph2<tm1.2Sna>/Diaph2<tm1.2Sna>	B6N.Cg-Diaph2<tm1.2Sna>	N	22246438
MGI:5606187	M	MP:0002169	no abnormal phenotype detected	Diaph2<tm1.2Sna>/Y	B6N.Cg-Diaph2<tm1.2Sna>	N	22246438
MGI:5606188	F	MP:0009949	abnormal olfactory bulb granule cell layer morphology	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Diaph2<tm1.2Sna>	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	N	22246438
MGI:5606188	F	MP:0000787	abnormal telencephalon morphology	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Diaph2<tm1.2Sna>	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	N	22246438
MGI:5606188	F	MP:0000819	abnormal olfactory bulb morphology	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Diaph2<tm1.2Sna>	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	N	22246438
MGI:5606188	F	MP:0006009	abnormal neuronal migration	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Diaph2<tm1.2Sna>	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	N	22246438
MGI:5606188	F	MP:0002741	small olfactory bulb	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Diaph2<tm1.2Sna>	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	N	22246438
MGI:5606188	F	MP:0003631	nervous system phenotype	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Diaph2<tm1.2Sna>	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	Y	22246438
MGI:5606188	F	MP:0000788	abnormal cerebral cortex morphology	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Diaph2<tm1.2Sna>	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	N	22246438
MGI:5606189	M	MP:0000788	abnormal cerebral cortex morphology	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Y	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	N	22246438
MGI:5606189	M	MP:0002741	small olfactory bulb	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Y	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	N	22246438
MGI:5606189	M	MP:0000819	abnormal olfactory bulb morphology	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Y	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	N	22246438
MGI:5606189	M	MP:0000787	abnormal telencephalon morphology	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Y	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	N	22246438
MGI:5606189	M	MP:0009949	abnormal olfactory bulb granule cell layer morphology	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Y	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	N	22246438
MGI:5606189	M	MP:0003631	nervous system phenotype	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Y	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	Y	22246438
MGI:5606189	M	MP:0006009	abnormal neuronal migration	Diaph1<tm1.1Sna>/Diaph1<tm1.1Sna>,Diaph2<tm1.2Sna>/Y	B6N.Cg-Diaph1<tm1.1Sna> Diahp2<tm1.2Sna>	N	22246438
MGI:5606285	F	MP:0004805	absent oocytes	mt-Tk<m1>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24510903
MGI:5607315	M	MP:0001516	abnormal motor coordination/balance	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607315	M	MP:0005394	taste/olfaction phenotype	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	Y	25100603
MGI:5607315	M	MP:0003354	astrocytosis	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607315	M	MP:0014370	impaired spatial working memory	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607315	M	MP:0001407	short stride length	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607315	M	MP:0002229	neurodegeneration	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607315	M	MP:0011620	abnormal habituation to a new environment	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607315	M	MP:0004191	neuronal intranuclear inclusions	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607315	M	MP:0003632	abnormal nervous system morphology	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607315	M	MP:0001364	decreased anxiety-related response	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607315	M	MP:0001402	decreased locomotor activity	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607315	M	MP:0001262	decreased body weight	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607315	M	MP:0002969	impaired social transmission of food preference	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607315	M	MP:0008414	abnormal spatial reference memory	Hprt1<tm5(Camk2a-BACE1)Geno>/Y	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607316	F	MP:0003632	abnormal nervous system morphology	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607316	F	MP:0001364	decreased anxiety-related response	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607316	F	MP:0001262	decreased body weight	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607316	F	MP:0002229	neurodegeneration	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607316	F	MP:0001516	abnormal motor coordination/balance	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607316	F	MP:0001407	short stride length	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607316	F	MP:0004191	neuronal intranuclear inclusions	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607316	F	MP:0002969	impaired social transmission of food preference	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607316	F	MP:0014370	impaired spatial working memory	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607316	F	MP:0003354	astrocytosis	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607316	F	MP:0011620	abnormal habituation to a new environment	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607316	F	MP:0001402	decreased locomotor activity	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607316	F	MP:0005394	taste/olfaction phenotype	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	Y	25100603
MGI:5607316	F	MP:0008414	abnormal spatial reference memory	Hprt1<tm5(Camk2a-BACE1)Geno>/Hprt1<tm5(Camk2a-BACE1)Geno>	B6.129P2-Hprt1<tm5(Camk2a-BACE1)Geno>	N	25100603
MGI:5607531	M	MP:0005459	decreased percent body fat/body weight	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0000135	decreased compact bone thickness	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	24550297
MGI:5607531	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0001262	decreased body weight	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0005560	decreased circulating glucose level	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0002644	decreased circulating triglyceride level	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0002891	increased insulin sensitivity	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0010873	decreased trabecular bone mass	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	24550297
MGI:5607531	M	MP:0008844	decreased subcutaneous adipose tissue amount	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0009346	decreased trabecular bone thickness	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	24550297
MGI:5607531	M	MP:0010869	decreased bone trabecula number	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	24550297
MGI:5607531	M	MP:0008396	abnormal osteoclast differentiation	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	24550297
MGI:5607531	M	MP:0000601	small liver	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0009133	decreased white fat cell size	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0000066	osteoporosis	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	24550297
MGI:5607531	M	MP:0004984	increased osteoclast cell number	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	24550297
MGI:5607531	M	MP:0004992	increased bone resorption	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	24550297
MGI:5607531	M	MP:0001258	decreased body length	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0005289	increased oxygen consumption	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0009136	decreased brown fat cell size	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0005659	decreased susceptibility to diet-induced obesity	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0000130	abnormal trabecular bone morphology	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	24550297
MGI:5607531	M	MP:0000063	decreased bone mineral density	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	24550297
MGI:5607531	M	MP:0005292	improved glucose tolerance	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0013278	decreased fasting circulating glucose level	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0014143	decreased body fat mass	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607531	M	MP:0002113	abnormal skeleton development	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	24550297
MGI:5607531	M	MP:0002896	abnormal bone mineralization	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	24550297
MGI:5607531	M	MP:0009703	decreased birth body size	Cnot3<tm1.1Tya>/Cnot3<+>	B6.129P2(Cg)-Cnot3<tm1.1Tya>	N	21897366
MGI:5607532	M	MP:0005386	behavior/neurological phenotype	Cnot3<tm1.1Tya>/Cnot3<+>,Lep<ob>/Lep<ob>	involves: 129P2/OlaHsd * C57BL/6J	Y	21897366
MGI:5607532	M	MP:0005292	improved glucose tolerance	Cnot3<tm1.1Tya>/Cnot3<+>,Lep<ob>/Lep<ob>	involves: 129P2/OlaHsd * C57BL/6J	N	21897366
MGI:5607532	M	MP:0001262	decreased body weight	Cnot3<tm1.1Tya>/Cnot3<+>,Lep<ob>/Lep<ob>	involves: 129P2/OlaHsd * C57BL/6J	N	21897366
MGI:5607532	M	MP:0002891	increased insulin sensitivity	Cnot3<tm1.1Tya>/Cnot3<+>,Lep<ob>/Lep<ob>	involves: 129P2/OlaHsd * C57BL/6J	N	21897366
MGI:5607532	M	MP:0005289	increased oxygen consumption	Cnot3<tm1.1Tya>/Cnot3<+>,Lep<ob>/Lep<ob>	involves: 129P2/OlaHsd * C57BL/6J	N	21897366
MGI:5607532	M	MP:0010379	decreased respiratory quotient	Cnot3<tm1.1Tya>/Cnot3<+>,Lep<ob>/Lep<ob>	involves: 129P2/OlaHsd * C57BL/6J	N	21897366
MGI:5607618	F	MP:0003982	increased cholesterol level	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Speer6-ps1<Tg(Alb-cre)21Mgn>/?	involves: C57BL/6 * DBA * SJL	N	25378657
MGI:5607618	F	MP:0005179	decreased circulating cholesterol level	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Speer6-ps1<Tg(Alb-cre)21Mgn>/?	involves: C57BL/6 * DBA * SJL	N	25378657
MGI:5607618	F	MP:0010078	increased circulating phytosterol level	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Speer6-ps1<Tg(Alb-cre)21Mgn>/?	involves: C57BL/6 * DBA * SJL	N	25378657
MGI:5607618	M	MP:0003193	decreased cholesterol efflux	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Speer6-ps1<Tg(Alb-cre)21Mgn>/?	involves: C57BL/6 * DBA * SJL	N	25378657
MGI:5607618	F	MP:0013437	decreased phytosterol level	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Speer6-ps1<Tg(Alb-cre)21Mgn>/?	involves: C57BL/6 * DBA * SJL	N	25378657
MGI:5607628	F	MP:0003983	decreased cholesterol level	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Tg(CAG-cre/Esr1*)5Amc/?	involves: C57BL/6 * CBA * SJL	N	25378657
MGI:5607628	M	MP:0003193	decreased cholesterol efflux	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Tg(CAG-cre/Esr1*)5Amc/?	involves: C57BL/6 * CBA * SJL	N	25378657
MGI:5607628	M	MP:0013756	increased intestinal phytosterol absorption	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Tg(CAG-cre/Esr1*)5Amc/?	involves: C57BL/6 * CBA * SJL	N	25378657
MGI:5607628	F	MP:0013437	decreased phytosterol level	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Tg(CAG-cre/Esr1*)5Amc/?	involves: C57BL/6 * CBA * SJL	N	25378657
MGI:5607628	M	MP:0003868	abnormal feces composition	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Tg(CAG-cre/Esr1*)5Amc/?	involves: C57BL/6 * CBA * SJL	N	25378657
MGI:5607628	F	MP:0010077	increased phytosterol level	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Tg(CAG-cre/Esr1*)5Amc/?	involves: C57BL/6 * CBA * SJL	N	25378657
MGI:5607628	F	MP:0005179	decreased circulating cholesterol level	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Tg(CAG-cre/Esr1*)5Amc/?	involves: C57BL/6 * CBA * SJL	N	25378657
MGI:5607632	F	MP:0010077	increased phytosterol level	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Tg(Vil1-cre)997Gum/?	involves: C57BL/6 * SJL	N	25378657
MGI:5607632	F	MP:0010078	increased circulating phytosterol level	Abcg5<tm1.1Hobb>/Abcg5<tm1.1Hobb>,Abcg8<tm1.1Hobb>/Abcg8<tm1.1Hobb>,Tg(Vil1-cre)997Gum/?	involves: C57BL/6 * SJL	N	25378657
MGI:5607746	M	MP:0008572	abnormal Purkinje cell dendrite morphology	Stk38l<Gt(RRT116)Byg>/Stk38l<Gt(RRT116)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24719112
MGI:5607777	M	MP:0004859	abnormal synaptic plasticity	Cnr1<tm1.1Kpm>/Cnr1<tm1.1Kpm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	24719095
MGI:5607777	M	MP:0001981	increased chemically-elicited antinociception	Cnr1<tm1.1Kpm>/Cnr1<tm1.1Kpm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	24719095
MGI:5607777	M	MP:0004811	abnormal neuron physiology	Cnr1<tm1.1Kpm>/Cnr1<tm1.1Kpm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	24719095
MGI:5607777	M	MP:0008873	increased physiological sensitivity to xenobiotic	Cnr1<tm1.1Kpm>/Cnr1<tm1.1Kpm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	24719095
MGI:5607777	M	MP:0000788	abnormal cerebral cortex morphology	Cnr1<tm1.1Kpm>/Cnr1<tm1.1Kpm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	24719095
MGI:5607777	M	MP:0009775	increased behavioral withdrawal response	Cnr1<tm1.1Kpm>/Cnr1<tm1.1Kpm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	24719095
MGI:5607934	M	MP:0005389	reproductive system phenotype	Semg1<tm1Kemi>/Semg1<tm1Kemi>	involves: 129 * C57BL/6N	Y	24591616
MGI:5607934	M	MP:0001922	reduced male fertility	Semg1<tm1Kemi>/Semg1<tm1Kemi>	involves: 129 * C57BL/6N	N	24591616
MGI:5607934	M	MP:0004543	abnormal sperm physiology	Semg1<tm1Kemi>/Semg1<tm1Kemi>	involves: 129 * C57BL/6N	N	24591616
MGI:5607934	M	MP:0030983	failure of copulatory plug deposition	Semg1<tm1Kemi>/Semg1<tm1Kemi>	involves: 129 * C57BL/6N	N	24591616
MGI:5607935	M	MP:0004543	abnormal sperm physiology	Semg1<tm1Kemi>/Semg1<tm1Kemi>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: 129 * C57BL/6 * C57BL/6N * DBA/2	N	24591616
MGI:5607935	M	MP:0013288	premature acrosome reaction	Semg1<tm1Kemi>/Semg1<tm1Kemi>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: 129 * C57BL/6 * C57BL/6N * DBA/2	N	24591616
MGI:5607935	M	MP:0002674	abnormal sperm motility	Semg1<tm1Kemi>/Semg1<tm1Kemi>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: 129 * C57BL/6 * C57BL/6N * DBA/2	N	24591616
MGI:5607936	M	MP:0001922	reduced male fertility	Semg1<tm2Kemi>/Semg1<tm2Kemi>	involves: 129 * C57BL/6N	N	24591616
MGI:5607936	M	MP:0004543	abnormal sperm physiology	Semg1<tm2Kemi>/Semg1<tm2Kemi>	involves: 129 * C57BL/6N	N	24591616
MGI:5607936	M	MP:0005389	reproductive system phenotype	Semg1<tm2Kemi>/Semg1<tm2Kemi>	involves: 129 * C57BL/6N	Y	24591616
MGI:5607936	M	MP:0003698	abnormal male reproductive system physiology	Semg1<tm2Kemi>/Semg1<tm2Kemi>	involves: 129 * C57BL/6N	N	24591616
MGI:5607937	M	MP:0004543	abnormal sperm physiology	Semg1<tm2Kemi>/Semg1<tm2Kemi>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: 129 * C57BL/6 * C57BL/6N * DBA/2	N	24591616
MGI:5607937	M	MP:0002674	abnormal sperm motility	Semg1<tm2Kemi>/Semg1<tm2Kemi>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: 129 * C57BL/6 * C57BL/6N * DBA/2	N	24591616
MGI:5607937	M	MP:0013288	premature acrosome reaction	Semg1<tm2Kemi>/Semg1<tm2Kemi>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: 129 * C57BL/6 * C57BL/6N * DBA/2	N	24591616
MGI:5607938	M	MP:0005389	reproductive system phenotype	Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: C57BL/6 * DBA/2	Y	20224175
MGI:5608227	M	MP:0001512	trunk curl	Ogfod3<tm1b(KOMP)Wtsi>/Ogfod3<tm1b(KOMP)Wtsi>	C57BL/6N-Ogfod3<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608227	M	MP:0001399	hyperactivity	Ogfod3<tm1b(KOMP)Wtsi>/Ogfod3<tm1b(KOMP)Wtsi>	C57BL/6N-Ogfod3<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608241	F	MP:0003795	abnormal bone structure	Ghrhr<tm1.1(KOMP)Vlcg>/Ghrhr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ghrhr<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608241	F	MP:0011396	abnormal sleep behavior	Ghrhr<tm1.1(KOMP)Vlcg>/Ghrhr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ghrhr<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608241	M	MP:0001552	increased circulating triglyceride level	Ghrhr<tm1.1(KOMP)Vlcg>/Ghrhr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ghrhr<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608241	M	MP:0003179	thrombocytopenia	Ghrhr<tm1.1(KOMP)Vlcg>/Ghrhr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ghrhr<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608241	M	MP:0005560	decreased circulating glucose level	Ghrhr<tm1.1(KOMP)Vlcg>/Ghrhr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ghrhr<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608241	F	MP:0005562	decreased mean corpuscular hemoglobin	Ghrhr<tm1.1(KOMP)Vlcg>/Ghrhr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ghrhr<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608244	F	MP:0013279	increased fasting circulating glucose level	Macrod2<tm1.1(KOMP)Vlcg>/Macrod2<+>	C57BL/6N-Macrod2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608244	M	MP:0005560	decreased circulating glucose level	Macrod2<tm1.1(KOMP)Vlcg>/Macrod2<+>	C57BL/6N-Macrod2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608245	F	MP:0001325	abnormal retina morphology	Macrod2<tm1.1(KOMP)Vlcg>/Macrod2<tm1.1(KOMP)Vlcg>	C57BL/6N-Macrod2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608245	M	MP:0005565	increased blood urea nitrogen level	Macrod2<tm1.1(KOMP)Vlcg>/Macrod2<tm1.1(KOMP)Vlcg>	C57BL/6N-Macrod2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608245	F	MP:0013279	increased fasting circulating glucose level	Macrod2<tm1.1(KOMP)Vlcg>/Macrod2<tm1.1(KOMP)Vlcg>	C57BL/6N-Macrod2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608245	F	MP:0002574	increased vertical activity	Macrod2<tm1.1(KOMP)Vlcg>/Macrod2<tm1.1(KOMP)Vlcg>	C57BL/6N-Macrod2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608247	M	MP:0001325	abnormal retina morphology	Dixdc1<tm1.1(KOMP)Vlcg>/Dixdc1<+>	C57BL/6N-Dixdc1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608248	M	MP:0001489	decreased startle reflex	Dixdc1<tm1.1(KOMP)Vlcg>/Dixdc1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dixdc1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608249	M	MP:0005560	decreased circulating glucose level	Med11<tm1.1(KOMP)Vlcg>/Med11<+>	C57BL/6N-Med11<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608249	M	MP:0013279	increased fasting circulating glucose level	Med11<tm1.1(KOMP)Vlcg>/Med11<+>	C57BL/6N-Med11<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608249	M	MP:0000195	decreased circulating calcium level	Med11<tm1.1(KOMP)Vlcg>/Med11<+>	C57BL/6N-Med11<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608250	M	MP:0000955	abnormal spinal cord morphology	Stk16<tm1.1(KOMP)Vlcg>/Stk16<tm1.1(KOMP)Vlcg>	C57BL/6N-Stk16<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608250	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Stk16<tm1.1(KOMP)Vlcg>/Stk16<tm1.1(KOMP)Vlcg>	C57BL/6N-Stk16<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608252	F	MP:0001297	microphthalmia	Dnajc5g<tm1.1(KOMP)Vlcg>/Dnajc5g<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajc5g<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608252	M	MP:0010053	decreased grip strength	Dnajc5g<tm1.1(KOMP)Vlcg>/Dnajc5g<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajc5g<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608253	F	MP:0002079	increased circulating insulin level	Dnajc5g<tm1.1(KOMP)Vlcg>/Dnajc5g<+>	C57BL/6N-Dnajc5g<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608254	F	MP:0011396	abnormal sleep behavior	Jam3<tm1.1(KOMP)Vlcg>/Jam3<+>	C57BL/6N-Jam3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608254	F	MP:0000759	abnormal skeletal muscle morphology	Jam3<tm1.1(KOMP)Vlcg>/Jam3<+>	C57BL/6N-Jam3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608257	M	MP:0000266	abnormal heart morphology	Cinp<tm1.1(KOMP)Vlcg>/Cinp<+>	B6N(Cg)-Cinp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5608259	F	MP:0001513	limb grasping	Nrcam<tm2e.1(KOMP)Wtsi>/Nrcam<+>	C57BL/6N-Nrcam<tm2e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5608259	M	MP:0013279	increased fasting circulating glucose level	Nrcam<tm2e.1(KOMP)Wtsi>/Nrcam<+>	C57BL/6N-Nrcam<tm2e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5608356	M	MP:0002606	increased basophil cell number	Gp9<tm1.1(KOMP)Vlcg>/Gp9<tm1.1(KOMP)Vlcg>	C57BL/6N-Gp9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5608361	M	MP:0010025	decreased total body fat amount	Mturn<tm1.1(KOMP)Vlcg>/Mturn<tm1.1(KOMP)Vlcg>	C57BL/6N-Mturn<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5608361	M	MP:0000367	abnormal coat/ hair morphology	Mturn<tm1.1(KOMP)Vlcg>/Mturn<tm1.1(KOMP)Vlcg>	C57BL/6N-Mturn<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5608361	M	MP:0003960	increased lean body mass	Mturn<tm1.1(KOMP)Vlcg>/Mturn<tm1.1(KOMP)Vlcg>	C57BL/6N-Mturn<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5608361	M	MP:0010123	increased bone mineral content	Mturn<tm1.1(KOMP)Vlcg>/Mturn<tm1.1(KOMP)Vlcg>	C57BL/6N-Mturn<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5608361	M	MP:0000062	increased bone mineral density	Mturn<tm1.1(KOMP)Vlcg>/Mturn<tm1.1(KOMP)Vlcg>	C57BL/6N-Mturn<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5608362	M	MP:0010025	decreased total body fat amount	Pcdh18<tm1.1(KOMP)Vlcg>/Pcdh18<tm1.1(KOMP)Vlcg>	C57BL/6N-Pcdh18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5608362	M	MP:0003960	increased lean body mass	Pcdh18<tm1.1(KOMP)Vlcg>/Pcdh18<tm1.1(KOMP)Vlcg>	C57BL/6N-Pcdh18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5608362	F	MP:0003900	shortened QT interval	Pcdh18<tm1.1(KOMP)Vlcg>/Pcdh18<tm1.1(KOMP)Vlcg>	C57BL/6N-Pcdh18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5608362	F	MP:0001314	cornea opacity	Pcdh18<tm1.1(KOMP)Vlcg>/Pcdh18<tm1.1(KOMP)Vlcg>	C57BL/6N-Pcdh18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5608362	F	MP:0010571	shortened ST segment	Pcdh18<tm1.1(KOMP)Vlcg>/Pcdh18<tm1.1(KOMP)Vlcg>	C57BL/6N-Pcdh18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5608362	F	MP:0002764	short tibia	Pcdh18<tm1.1(KOMP)Vlcg>/Pcdh18<tm1.1(KOMP)Vlcg>	C57BL/6N-Pcdh18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5608363	M	MP:0005553	increased circulating creatinine level	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608363	M	MP:0010092	increased circulating magnesium level	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608363	F	MP:0003019	increased circulating chloride level	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608364	M	MP:0010067	increased red blood cell distribution width	Eps8l1<tm2b(KOMP)Wtsi>/Eps8l1<tm2b(KOMP)Wtsi>	C57BL/6N-Eps8l1<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5608366	F	MP:0001556	increased circulating HDL cholesterol level	Tm9sf4<tm1a(KOMP)Wtsi>/Tm9sf4<tm1a(KOMP)Wtsi>	C57BL/6N-Tm9sf4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608366	F	MP:0010099	abnormal thoracic cage shape	Tm9sf4<tm1a(KOMP)Wtsi>/Tm9sf4<tm1a(KOMP)Wtsi>	C57BL/6N-Tm9sf4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608366	F	MP:0005178	increased circulating cholesterol level	Tm9sf4<tm1a(KOMP)Wtsi>/Tm9sf4<tm1a(KOMP)Wtsi>	C57BL/6N-Tm9sf4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608367	M	MP:0004174	abnormal spine curvature	Pabpc4<tm1a(KOMP)Wtsi>/Pabpc4<tm1a(KOMP)Wtsi>	C57BL/6N-Pabpc4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608367	M	MP:0002833	increased heart weight	Pabpc4<tm1a(KOMP)Wtsi>/Pabpc4<tm1a(KOMP)Wtsi>	C57BL/6N-Pabpc4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608374	M	MP:0000062	increased bone mineral density	Ddhd1<tm1a(KOMP)Wtsi>/Ddhd1<tm1a(KOMP)Wtsi>	C57BL/6N-Ddhd1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608374	M	MP:0003960	increased lean body mass	Ddhd1<tm1a(KOMP)Wtsi>/Ddhd1<tm1a(KOMP)Wtsi>	C57BL/6N-Ddhd1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608375	M	MP:0003019	increased circulating chloride level	Gimap6<tm1a(KOMP)Wtsi>/Gimap6<tm1a(KOMP)Wtsi>	C57BL/6N-Gimap6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608375	M	MP:0005293	impaired glucose tolerance	Gimap6<tm1a(KOMP)Wtsi>/Gimap6<tm1a(KOMP)Wtsi>	C57BL/6N-Gimap6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608375	M	MP:0003961	decreased lean body mass	Gimap6<tm1a(KOMP)Wtsi>/Gimap6<tm1a(KOMP)Wtsi>	C57BL/6N-Gimap6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608380	M	MP:0001325	abnormal retina morphology	Aldh16a1<tm1a(EUCOMM)Wtsi>/Aldh16a1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aldh16a1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608382	M	MP:0010067	increased red blood cell distribution width	Mettl24<tm1a(KOMP)Wtsi>/Mettl24<tm1a(KOMP)Wtsi>	C57BL/6N-Mettl24<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608382	M	MP:0010123	increased bone mineral content	Mettl24<tm1a(KOMP)Wtsi>/Mettl24<tm1a(KOMP)Wtsi>	C57BL/6N-Mettl24<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608382	M	MP:0003960	increased lean body mass	Mettl24<tm1a(KOMP)Wtsi>/Mettl24<tm1a(KOMP)Wtsi>	C57BL/6N-Mettl24<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608382	M	MP:0010025	decreased total body fat amount	Mettl24<tm1a(KOMP)Wtsi>/Mettl24<tm1a(KOMP)Wtsi>	C57BL/6N-Mettl24<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608382	F	MP:0002968	increased circulating alkaline phosphatase level	Mettl24<tm1a(KOMP)Wtsi>/Mettl24<tm1a(KOMP)Wtsi>	C57BL/6N-Mettl24<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608384	M	MP:0011939	increased food intake	Leprot<tm2a(KOMP)Wtsi>/Leprot<tm2a(KOMP)Wtsi>	C57BL/6N-Leprot<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608384	M	MP:0010123	increased bone mineral content	Leprot<tm2a(KOMP)Wtsi>/Leprot<tm2a(KOMP)Wtsi>	C57BL/6N-Leprot<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608384	M	MP:0003960	increased lean body mass	Leprot<tm2a(KOMP)Wtsi>/Leprot<tm2a(KOMP)Wtsi>	C57BL/6N-Leprot<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608384	M	MP:0010067	increased red blood cell distribution width	Leprot<tm2a(KOMP)Wtsi>/Leprot<tm2a(KOMP)Wtsi>	C57BL/6N-Leprot<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608384	M	MP:0010025	decreased total body fat amount	Leprot<tm2a(KOMP)Wtsi>/Leprot<tm2a(KOMP)Wtsi>	C57BL/6N-Leprot<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608385	F	MP:0002941	increased circulating alanine transaminase level	Dhrs2<tm1a(KOMP)Wtsi>/Dhrs2<tm1a(KOMP)Wtsi>	C57BL/6N-Dhrs2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608386	F	MP:0000186	decreased circulating HDL cholesterol level	Wdtc1<tm1a(KOMP)Wtsi>/Wdtc1<tm1a(KOMP)Wtsi>	C57BL/6N-Wdtc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608386	M	MP:0013278	decreased fasting circulating glucose level	Wdtc1<tm1a(KOMP)Wtsi>/Wdtc1<tm1a(KOMP)Wtsi>	C57BL/6N-Wdtc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608387	F	MP:0003795	abnormal bone structure	Scn3b<tm1a(KOMP)Wtsi>/Scn3b<tm1a(KOMP)Wtsi>	C57BL/6N-Scn3b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608387	F	MP:0004510	myositis	Scn3b<tm1a(KOMP)Wtsi>/Scn3b<tm1a(KOMP)Wtsi>	C57BL/6N-Scn3b<tm1a(KOMP)Wtsi>/Wtsi	N	25340873
MGI:5608387	F	MP:0011157	abnormal hypodermis muscle layer morphology	Scn3b<tm1a(KOMP)Wtsi>/Scn3b<tm1a(KOMP)Wtsi>	C57BL/6N-Scn3b<tm1a(KOMP)Wtsi>/Wtsi	N	25340873
MGI:5608389	M	MP:0005292	improved glucose tolerance	Ush1c<tm1a(KOMP)Wtsi>/Ush1c<tm1a(KOMP)Wtsi>	C57BL/6N-Ush1c<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608389	M	MP:0010025	decreased total body fat amount	Ush1c<tm1a(KOMP)Wtsi>/Ush1c<tm1a(KOMP)Wtsi>	C57BL/6N-Ush1c<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608389	M	MP:0011939	increased food intake	Ush1c<tm1a(KOMP)Wtsi>/Ush1c<tm1a(KOMP)Wtsi>	C57BL/6N-Ush1c<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608389	M	MP:0008805	decreased circulating amylase level	Ush1c<tm1a(KOMP)Wtsi>/Ush1c<tm1a(KOMP)Wtsi>	C57BL/6N-Ush1c<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608389	M	MP:0005560	decreased circulating glucose level	Ush1c<tm1a(KOMP)Wtsi>/Ush1c<tm1a(KOMP)Wtsi>	C57BL/6N-Ush1c<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608389	M	MP:0010067	increased red blood cell distribution width	Ush1c<tm1a(KOMP)Wtsi>/Ush1c<tm1a(KOMP)Wtsi>	C57BL/6N-Ush1c<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608392	F	MP:0001325	abnormal retina morphology	Rtbdn<tm1a(EUCOMM)Wtsi>/Rtbdn<tm1a(EUCOMM)Wtsi>	C57BL/6N-Rtbdn<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608392	M	MP:0005505	thrombocytosis	Rtbdn<tm1a(EUCOMM)Wtsi>/Rtbdn<tm1a(EUCOMM)Wtsi>	C57BL/6N-Rtbdn<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608392	M	MP:0005292	improved glucose tolerance	Rtbdn<tm1a(EUCOMM)Wtsi>/Rtbdn<tm1a(EUCOMM)Wtsi>	C57BL/6N-Rtbdn<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608393	F	MP:0000063	decreased bone mineral density	Alg13<tm1a(KOMP)Wtsi>/Alg13<tm1a(KOMP)Wtsi>	C57BL/6N-Alg13<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608393	F	MP:0003961	decreased lean body mass	Alg13<tm1a(KOMP)Wtsi>/Alg13<tm1a(KOMP)Wtsi>	C57BL/6N-Alg13<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608393	F	MP:0010124	decreased bone mineral content	Alg13<tm1a(KOMP)Wtsi>/Alg13<tm1a(KOMP)Wtsi>	C57BL/6N-Alg13<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608393	F	MP:0000218	increased leukocyte cell number	Alg13<tm1a(KOMP)Wtsi>/Alg13<tm1a(KOMP)Wtsi>	C57BL/6N-Alg13<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608393	F	MP:0010024	increased total body fat amount	Alg13<tm1a(KOMP)Wtsi>/Alg13<tm1a(KOMP)Wtsi>	C57BL/6N-Alg13<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608394	M	MP:0004151	decreased circulating iron level	Cand2<tm1a(EUCOMM)Wtsi>/Cand2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cand2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608394	M	MP:0010025	decreased total body fat amount	Cand2<tm1a(EUCOMM)Wtsi>/Cand2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cand2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608394	M	MP:0003960	increased lean body mass	Cand2<tm1a(EUCOMM)Wtsi>/Cand2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cand2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608394	M	MP:0010067	increased red blood cell distribution width	Cand2<tm1a(EUCOMM)Wtsi>/Cand2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cand2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608394	M	MP:0005478	decreased circulating thyroxine level	Cand2<tm1a(EUCOMM)Wtsi>/Cand2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cand2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608396	M	MP:0000218	increased leukocyte cell number	Ralb<tm1a(EUCOMM)Wtsi>/Ralb<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ralb<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608397	M	MP:0003960	increased lean body mass	Snap47<tm1a(EUCOMM)Wtsi>/Snap47<tm1a(EUCOMM)Wtsi>	C57BL/6N-Snap47<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608397	F	MP:0003961	decreased lean body mass	Snap47<tm1a(EUCOMM)Wtsi>/Snap47<tm1a(EUCOMM)Wtsi>	C57BL/6N-Snap47<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608397	M	MP:0000062	increased bone mineral density	Snap47<tm1a(EUCOMM)Wtsi>/Snap47<tm1a(EUCOMM)Wtsi>	C57BL/6N-Snap47<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608397	M	MP:0010123	increased bone mineral content	Snap47<tm1a(EUCOMM)Wtsi>/Snap47<tm1a(EUCOMM)Wtsi>	C57BL/6N-Snap47<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608397	M	MP:0010025	decreased total body fat amount	Snap47<tm1a(EUCOMM)Wtsi>/Snap47<tm1a(EUCOMM)Wtsi>	C57BL/6N-Snap47<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608398	M	MP:0003960	increased lean body mass	Sag<tm1a(EUCOMM)Wtsi>/Sag<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sag<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608398	M	MP:0000195	decreased circulating calcium level	Sag<tm1a(EUCOMM)Wtsi>/Sag<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sag<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608398	M	MP:0000186	decreased circulating HDL cholesterol level	Sag<tm1a(EUCOMM)Wtsi>/Sag<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sag<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608398	M	MP:0010025	decreased total body fat amount	Sag<tm1a(EUCOMM)Wtsi>/Sag<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sag<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608398	M	MP:0010088	decreased circulating fructosamine level	Sag<tm1a(EUCOMM)Wtsi>/Sag<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sag<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608401	M	MP:0010052	increased grip strength	Lamc3<tm1a(KOMP)Wtsi>/Lamc3<tm1a(KOMP)Wtsi>	C57BL/6N-Lamc3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608401	M	MP:0003179	thrombocytopenia	Lamc3<tm1a(KOMP)Wtsi>/Lamc3<tm1a(KOMP)Wtsi>	C57BL/6N-Lamc3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608402	M	MP:0011939	increased food intake	Dppa1<tm1a(KOMP)Wtsi>/Dppa1<tm1a(KOMP)Wtsi>	C57BL/6N-Dppa1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608402	M	MP:0000062	increased bone mineral density	Dppa1<tm1a(KOMP)Wtsi>/Dppa1<tm1a(KOMP)Wtsi>	C57BL/6N-Dppa1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608402	M	MP:0010378	increased respiratory quotient	Dppa1<tm1a(KOMP)Wtsi>/Dppa1<tm1a(KOMP)Wtsi>	C57BL/6N-Dppa1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608402	M	MP:0003960	increased lean body mass	Dppa1<tm1a(KOMP)Wtsi>/Dppa1<tm1a(KOMP)Wtsi>	C57BL/6N-Dppa1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608403	M	MP:0005343	increased circulating aspartate transaminase level	Setd4<tm1a(KOMP)Wtsi>/Setd4<tm1a(KOMP)Wtsi>	C57BL/6N-Setd4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608403	M	MP:0013278	decreased fasting circulating glucose level	Setd4<tm1a(KOMP)Wtsi>/Setd4<tm1a(KOMP)Wtsi>	C57BL/6N-Setd4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608404	M	MP:0003179	thrombocytopenia	Dsg1b<tm1a(KOMP)Wtsi>/Dsg1b<tm1a(KOMP)Wtsi>	C57BL/6N-Dsg1b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608404	F	MP:0001322	abnormal iris morphology	Dsg1b<tm1a(KOMP)Wtsi>/Dsg1b<tm1a(KOMP)Wtsi>	C57BL/6N-Dsg1b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608404	M	MP:0010123	increased bone mineral content	Dsg1b<tm1a(KOMP)Wtsi>/Dsg1b<tm1a(KOMP)Wtsi>	C57BL/6N-Dsg1b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608404	M	MP:0001510	abnormal coat appearance	Dsg1b<tm1a(KOMP)Wtsi>/Dsg1b<tm1a(KOMP)Wtsi>	C57BL/6N-Dsg1b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608404	F	MP:0001312	abnormal cornea morphology	Dsg1b<tm1a(KOMP)Wtsi>/Dsg1b<tm1a(KOMP)Wtsi>	C57BL/6N-Dsg1b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608404	F	MP:0001304	cataract	Dsg1b<tm1a(KOMP)Wtsi>/Dsg1b<tm1a(KOMP)Wtsi>	C57BL/6N-Dsg1b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608404	F	MP:0001303	abnormal lens morphology	Dsg1b<tm1a(KOMP)Wtsi>/Dsg1b<tm1a(KOMP)Wtsi>	C57BL/6N-Dsg1b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608405	M	MP:0000443	abnormal snout morphology	Aff3<tm1a(EUCOMM)Wtsi>/Aff3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aff3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608405	M	MP:0005358	abnormal incisor morphology	Aff3<tm1a(EUCOMM)Wtsi>/Aff3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aff3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608405	M	MP:0000781	decreased corpus callosum size	Aff3<tm1a(EUCOMM)Wtsi>/Aff3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aff3<tm1a(EUCOMM)Wtsi>/Wtsi	N	33961779
MGI:5608405	M	MP:0010088	decreased circulating fructosamine level	Aff3<tm1a(EUCOMM)Wtsi>/Aff3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aff3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608405	F	MP:0010053	decreased grip strength	Aff3<tm1a(EUCOMM)Wtsi>/Aff3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aff3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608405	M	MP:0003019	increased circulating chloride level	Aff3<tm1a(EUCOMM)Wtsi>/Aff3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aff3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608405	M	MP:0008535	enlarged lateral ventricles	Aff3<tm1a(EUCOMM)Wtsi>/Aff3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aff3<tm1a(EUCOMM)Wtsi>/Wtsi	N	33961779
MGI:5608405	F	MP:0002968	increased circulating alkaline phosphatase level	Aff3<tm1a(EUCOMM)Wtsi>/Aff3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aff3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608405	F	MP:0003036	vertebral transformation	Aff3<tm1a(EUCOMM)Wtsi>/Aff3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aff3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608405	F	MP:0004613	fusion of vertebral arches	Aff3<tm1a(EUCOMM)Wtsi>/Aff3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aff3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608406	F	MP:0010096	abnormal incisor color	Slc20a2<tm1a(EUCOMM)Wtsi>/Slc20a2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc20a2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608406	M	MP:0000160	kyphosis	Slc20a2<tm1a(EUCOMM)Wtsi>/Slc20a2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc20a2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608406	M	MP:0005176	eyelids fail to open	Slc20a2<tm1a(EUCOMM)Wtsi>/Slc20a2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc20a2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608406	F	MP:0000063	decreased bone mineral density	Slc20a2<tm1a(EUCOMM)Wtsi>/Slc20a2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc20a2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608406	M	MP:0004174	abnormal spine curvature	Slc20a2<tm1a(EUCOMM)Wtsi>/Slc20a2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc20a2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608406	F	MP:0002968	increased circulating alkaline phosphatase level	Slc20a2<tm1a(EUCOMM)Wtsi>/Slc20a2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc20a2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608406	F	MP:0006358	absent pinna reflex	Slc20a2<tm1a(EUCOMM)Wtsi>/Slc20a2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc20a2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608406	F	MP:0001322	abnormal iris morphology	Slc20a2<tm1a(EUCOMM)Wtsi>/Slc20a2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc20a2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608409	F	MP:0001325	abnormal retina morphology	Myo10<tm2(KOMP)Wtsi>/Myo10<tm2(KOMP)Wtsi>	C57BL/6N-Myo10<tm2(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608409	F	MP:0001314	cornea opacity	Myo10<tm2(KOMP)Wtsi>/Myo10<tm2(KOMP)Wtsi>	C57BL/6N-Myo10<tm2(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608409	F	MP:0001312	abnormal cornea morphology	Myo10<tm2(KOMP)Wtsi>/Myo10<tm2(KOMP)Wtsi>	C57BL/6N-Myo10<tm2(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608409	F	MP:0001413	abnormal response to new environment	Myo10<tm2(KOMP)Wtsi>/Myo10<tm2(KOMP)Wtsi>	C57BL/6N-Myo10<tm2(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608409	F	MP:0005554	decreased circulating creatinine level	Myo10<tm2(KOMP)Wtsi>/Myo10<tm2(KOMP)Wtsi>	C57BL/6N-Myo10<tm2(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608409	F	MP:0001307	fused cornea and lens	Myo10<tm2(KOMP)Wtsi>/Myo10<tm2(KOMP)Wtsi>	C57BL/6N-Myo10<tm2(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608409	F	MP:0006243	impaired pupillary reflex	Myo10<tm2(KOMP)Wtsi>/Myo10<tm2(KOMP)Wtsi>	C57BL/6N-Myo10<tm2(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608412	M	MP:0002968	increased circulating alkaline phosphatase level	Hsp90aa1<tm1(KOMP)Wtsi>/Hsp90aa1<tm1(KOMP)Wtsi>	C57BL/6N-Hsp90aa1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608412	M	MP:0001925	male infertility	Hsp90aa1<tm1(KOMP)Wtsi>/Hsp90aa1<tm1(KOMP)Wtsi>	C57BL/6N-Hsp90aa1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608412	F	MP:0010052	increased grip strength	Hsp90aa1<tm1(KOMP)Wtsi>/Hsp90aa1<tm1(KOMP)Wtsi>	C57BL/6N-Hsp90aa1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608414	M	MP:0001556	increased circulating HDL cholesterol level	Reg3g<tm1a(KOMP)Wtsi>/Reg3g<tm1a(KOMP)Wtsi>	C57BL/6N-Reg3g<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608415	F	MP:0001258	decreased body length	Nacad<tm1(KOMP)Wtsi>/Nacad<tm1(KOMP)Wtsi>	C57BL/6N-Nacad<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608415	F	MP:0002079	increased circulating insulin level	Nacad<tm1(KOMP)Wtsi>/Nacad<tm1(KOMP)Wtsi>	C57BL/6N-Nacad<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608415	M	MP:0005560	decreased circulating glucose level	Nacad<tm1(KOMP)Wtsi>/Nacad<tm1(KOMP)Wtsi>	C57BL/6N-Nacad<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608416	M	MP:0003179	thrombocytopenia	Aspm<tm1a(KOMP)Wtsi>/Aspm<tm1a(KOMP)Wtsi>	C57BL/6N-Aspm<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608416	M	MP:0003443	increased circulating glycerol level	Aspm<tm1a(KOMP)Wtsi>/Aspm<tm1a(KOMP)Wtsi>	C57BL/6N-Aspm<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608416	M	MP:0005178	increased circulating cholesterol level	Aspm<tm1a(KOMP)Wtsi>/Aspm<tm1a(KOMP)Wtsi>	C57BL/6N-Aspm<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608417	M	MP:0005560	decreased circulating glucose level	Il10rb<tm1a(KOMP)Wtsi>/Il10rb<tm1a(KOMP)Wtsi>	C57BL/6N-Il10rb<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608419	F	MP:0002968	increased circulating alkaline phosphatase level	Ahcyl1<tm1a(EUCOMM)Wtsi>/Ahcyl1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ahcyl1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608419	F	MP:0010123	increased bone mineral content	Ahcyl1<tm1a(EUCOMM)Wtsi>/Ahcyl1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ahcyl1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608419	F	MP:0001312	abnormal cornea morphology	Ahcyl1<tm1a(EUCOMM)Wtsi>/Ahcyl1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ahcyl1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608419	F	MP:0001325	abnormal retina morphology	Ahcyl1<tm1a(EUCOMM)Wtsi>/Ahcyl1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ahcyl1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608419	F	MP:0005477	increased circulating thyroxine level	Ahcyl1<tm1a(EUCOMM)Wtsi>/Ahcyl1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ahcyl1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608419	F	MP:0002599	increased mean platelet volume	Ahcyl1<tm1a(EUCOMM)Wtsi>/Ahcyl1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ahcyl1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608424	M	MP:0005565	increased blood urea nitrogen level	Ift80<tm1a(KOMP)Wtsi>/Ift80<tm1a(KOMP)Wtsi>	C57BL/6N-Ift80<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608424	M	MP:0004509	abnormal pelvic girdle bone morphology	Ift80<tm1a(KOMP)Wtsi>/Ift80<tm1a(KOMP)Wtsi>	C57BL/6N-Ift80<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608428	F	MP:0002968	increased circulating alkaline phosphatase level	Slc25a4<tm1a(EUCOMM)Wtsi>/Slc25a4<tm1a(EUCOMM)Wtsi>	C57BL/6N-A<tm1Brd> Slc25a4<tm1a(EUCOMM)Wtsi>/WtsiH	N	MGI:5576271
MGI:5608428	M	MP:0005565	increased blood urea nitrogen level	Slc25a4<tm1a(EUCOMM)Wtsi>/Slc25a4<tm1a(EUCOMM)Wtsi>	C57BL/6N-A<tm1Brd> Slc25a4<tm1a(EUCOMM)Wtsi>/WtsiH	N	MGI:5576271
MGI:5608431	F	MP:0003036	vertebral transformation	Kdm7a<tm1a(EUCOMM)Wtsi>/Kdm7a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kdm7a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608434	F	MP:0003795	abnormal bone structure	Pias2<tm1a(KOMP)Wtsi>/Pias2<tm1a(KOMP)Wtsi>	C57BL/6N-Pias2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608434	M	MP:0002110	abnormal digit morphology	Pias2<tm1a(KOMP)Wtsi>/Pias2<tm1a(KOMP)Wtsi>	C57BL/6N-Pias2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608434	M	MP:0002079	increased circulating insulin level	Pias2<tm1a(KOMP)Wtsi>/Pias2<tm1a(KOMP)Wtsi>	C57BL/6N-Pias2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608434	F	MP:0010024	increased total body fat amount	Pias2<tm1a(KOMP)Wtsi>/Pias2<tm1a(KOMP)Wtsi>	C57BL/6N-Pias2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608434	F	MP:0003961	decreased lean body mass	Pias2<tm1a(KOMP)Wtsi>/Pias2<tm1a(KOMP)Wtsi>	C57BL/6N-Pias2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608434	F	MP:0001258	decreased body length	Pias2<tm1a(KOMP)Wtsi>/Pias2<tm1a(KOMP)Wtsi>	C57BL/6N-Pias2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608434	F	MP:0010124	decreased bone mineral content	Pias2<tm1a(KOMP)Wtsi>/Pias2<tm1a(KOMP)Wtsi>	C57BL/6N-Pias2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608435	M	MP:0005565	increased blood urea nitrogen level	Myo7a<tm1a(EUCOMM)Wtsi>/Myo7a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Myo7a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608435	F	MP:0001289	persistence of hyaloid vascular system	Myo7a<tm1a(EUCOMM)Wtsi>/Myo7a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Myo7a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608436	M	MP:0005419	decreased circulating serum albumin level	Tff1<tm1a(EUCOMM)Wtsi>/Tff1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tff1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608436	M	MP:0005567	decreased circulating total protein level	Tff1<tm1a(EUCOMM)Wtsi>/Tff1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tff1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608436	M	MP:0003960	increased lean body mass	Tff1<tm1a(EUCOMM)Wtsi>/Tff1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tff1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608439	M	MP:0000194	increased circulating calcium level	Mrap2<tm1a(EUCOMM)Wtsi>/Mrap2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mrap2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608439	F	MP:0003795	abnormal bone structure	Mrap2<tm1a(EUCOMM)Wtsi>/Mrap2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mrap2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608439	M	MP:0010067	increased red blood cell distribution width	Mrap2<tm1a(EUCOMM)Wtsi>/Mrap2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mrap2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608439	M	MP:0002968	increased circulating alkaline phosphatase level	Mrap2<tm1a(EUCOMM)Wtsi>/Mrap2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mrap2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608439	M	MP:0002079	increased circulating insulin level	Mrap2<tm1a(EUCOMM)Wtsi>/Mrap2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mrap2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608446	M	MP:0005560	decreased circulating glucose level	Cbx5<tm1a(EUCOMM)Wtsi>/Cbx5<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cbx5<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608448	M	MP:0010123	increased bone mineral content	Cbx6<tm1a(EUCOMM)Wtsi>/Cbx6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cbx6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608448	F	MP:0008806	increased circulating amylase level	Cbx6<tm1a(EUCOMM)Wtsi>/Cbx6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cbx6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608448	M	MP:0005179	decreased circulating cholesterol level	Cbx6<tm1a(EUCOMM)Wtsi>/Cbx6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cbx6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608448	M	MP:0005560	decreased circulating glucose level	Cbx6<tm1a(EUCOMM)Wtsi>/Cbx6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cbx6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608448	M	MP:0013278	decreased fasting circulating glucose level	Cbx6<tm1a(EUCOMM)Wtsi>/Cbx6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cbx6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608448	F	MP:0005553	increased circulating creatinine level	Cbx6<tm1a(EUCOMM)Wtsi>/Cbx6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cbx6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608448	M	MP:0003960	increased lean body mass	Cbx6<tm1a(EUCOMM)Wtsi>/Cbx6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cbx6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608448	M	MP:0010025	decreased total body fat amount	Cbx6<tm1a(EUCOMM)Wtsi>/Cbx6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cbx6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608448	M	MP:0000558	abnormal tibia morphology	Cbx6<tm1a(EUCOMM)Wtsi>/Cbx6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cbx6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608456	F	MP:0001262	decreased body weight	Wdr37<tm1a(KOMP)Wtsi>/Wdr37<tm1a(KOMP)Wtsi>	C57BL/6N-Wdr37<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5608456	F	MP:0000194	increased circulating calcium level	Wdr37<tm1a(KOMP)Wtsi>/Wdr37<tm1a(KOMP)Wtsi>	C57BL/6N-Wdr37<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608456	F	MP:0002968	increased circulating alkaline phosphatase level	Wdr37<tm1a(KOMP)Wtsi>/Wdr37<tm1a(KOMP)Wtsi>	C57BL/6N-Wdr37<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608456	M	MP:0000221	decreased leukocyte cell number	Wdr37<tm1a(KOMP)Wtsi>/Wdr37<tm1a(KOMP)Wtsi>	C57BL/6N-Wdr37<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608456	M	MP:0004174	abnormal spine curvature	Wdr37<tm1a(KOMP)Wtsi>/Wdr37<tm1a(KOMP)Wtsi>	C57BL/6N-Wdr37<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608456	M	MP:0010123	increased bone mineral content	Wdr37<tm1a(KOMP)Wtsi>/Wdr37<tm1a(KOMP)Wtsi>	C57BL/6N-Wdr37<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608456	M	MP:0000160	kyphosis	Wdr37<tm1a(KOMP)Wtsi>/Wdr37<tm1a(KOMP)Wtsi>	C57BL/6N-Wdr37<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608456	M	MP:0004609	vertebral fusion	Wdr37<tm1a(KOMP)Wtsi>/Wdr37<tm1a(KOMP)Wtsi>	C57BL/6N-Wdr37<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608456	M	MP:0004613	fusion of vertebral arches	Wdr37<tm1a(KOMP)Wtsi>/Wdr37<tm1a(KOMP)Wtsi>	C57BL/6N-Wdr37<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608458	F	MP:0005344	increased circulating bilirubin level	Cyp20a1<tm1a(EUCOMM)Wtsi>/Cyp20a1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cyp20a1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608459	M	MP:0002875	decreased erythrocyte cell number	Ciao2a<tm2a(EUCOMM)Wtsi>/Ciao2a<tm2a(EUCOMM)Wtsi>	C57BL/6N-Ciao2a<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608461	M	MP:0002702	decreased circulating free fatty acids level	Dop1b<tm1a(EUCOMM)Wtsi>/Dop1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dop1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608461	F	MP:0005565	increased blood urea nitrogen level	Dop1b<tm1a(EUCOMM)Wtsi>/Dop1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dop1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608461	M	MP:0010052	increased grip strength	Dop1b<tm1a(EUCOMM)Wtsi>/Dop1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dop1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608461	M	MP:0001510	abnormal coat appearance	Dop1b<tm1a(EUCOMM)Wtsi>/Dop1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dop1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608461	M	MP:0003960	increased lean body mass	Dop1b<tm1a(EUCOMM)Wtsi>/Dop1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dop1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608461	M	MP:0000218	increased leukocyte cell number	Dop1b<tm1a(EUCOMM)Wtsi>/Dop1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dop1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608461	M	MP:0010123	increased bone mineral content	Dop1b<tm1a(EUCOMM)Wtsi>/Dop1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dop1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608461	M	MP:0000062	increased bone mineral density	Dop1b<tm1a(EUCOMM)Wtsi>/Dop1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dop1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608461	M	MP:0003442	decreased circulating glycerol level	Dop1b<tm1a(EUCOMM)Wtsi>/Dop1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dop1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608465	F	MP:0004609	vertebral fusion	Ushbp1<tm1a(EUCOMM)Wtsi>/Ushbp1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ushbp1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608466	M	MP:0000218	increased leukocyte cell number	Nbeal2<tm1a(EUCOMM)Wtsi>/Nbeal2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Nbeal2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608466	M	MP:0010124	decreased bone mineral content	Nbeal2<tm1a(EUCOMM)Wtsi>/Nbeal2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Nbeal2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608466	M	MP:0000063	decreased bone mineral density	Nbeal2<tm1a(EUCOMM)Wtsi>/Nbeal2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Nbeal2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608468	M	MP:0000062	increased bone mineral density	Mlec<tm1a(EUCOMM)Wtsi>/Mlec<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mlec<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608468	M	MP:0003960	increased lean body mass	Mlec<tm1a(EUCOMM)Wtsi>/Mlec<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mlec<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608468	M	MP:0010123	increased bone mineral content	Mlec<tm1a(EUCOMM)Wtsi>/Mlec<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mlec<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608468	F	MP:0005477	increased circulating thyroxine level	Mlec<tm1a(EUCOMM)Wtsi>/Mlec<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mlec<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608471	F	MP:0001258	decreased body length	Tnik<tm3a(EUCOMM)Wtsi>/Tnik<tm3a(EUCOMM)Wtsi>	C57BL/6N-Tnik<tm3a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608471	F	MP:0004509	abnormal pelvic girdle bone morphology	Tnik<tm3a(EUCOMM)Wtsi>/Tnik<tm3a(EUCOMM)Wtsi>	C57BL/6N-Tnik<tm3a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608478	F	MP:0000438	abnormal cranium morphology	Daam2<tm1a(KOMP)Wtsi>/Daam2<tm1a(KOMP)Wtsi>	C57BL/6N-Daam2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608478	F	MP:0000443	abnormal snout morphology	Daam2<tm1a(KOMP)Wtsi>/Daam2<tm1a(KOMP)Wtsi>	C57BL/6N-Daam2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608478	F	MP:0013279	increased fasting circulating glucose level	Daam2<tm1a(KOMP)Wtsi>/Daam2<tm1a(KOMP)Wtsi>	C57BL/6N-Daam2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608478	F	MP:0002968	increased circulating alkaline phosphatase level	Daam2<tm1a(KOMP)Wtsi>/Daam2<tm1a(KOMP)Wtsi>	C57BL/6N-Daam2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608478	F	MP:0000455	abnormal maxilla morphology	Daam2<tm1a(KOMP)Wtsi>/Daam2<tm1a(KOMP)Wtsi>	C57BL/6N-Daam2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608478	F	MP:0001258	decreased body length	Daam2<tm1a(KOMP)Wtsi>/Daam2<tm1a(KOMP)Wtsi>	C57BL/6N-Daam2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608481	M	MP:0002833	increased heart weight	Gsto2<tm2a(KOMP)Wtsi>/Gsto2<tm2a(KOMP)Wtsi>	C57BL/6N-Gsto2<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608481	M	MP:0002098	abnormal vibrissa morphology	Gsto2<tm2a(KOMP)Wtsi>/Gsto2<tm2a(KOMP)Wtsi>	C57BL/6N-Gsto2<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608481	M	MP:0010123	increased bone mineral content	Gsto2<tm2a(KOMP)Wtsi>/Gsto2<tm2a(KOMP)Wtsi>	C57BL/6N-Gsto2<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608481	M	MP:0000062	increased bone mineral density	Gsto2<tm2a(KOMP)Wtsi>/Gsto2<tm2a(KOMP)Wtsi>	C57BL/6N-Gsto2<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608483	M	MP:0005419	decreased circulating serum albumin level	Adgrb1<tm2a(EUCOMM)Wtsi>/Adgrb1<tm2a(EUCOMM)Wtsi>	C57BL/6N-Adgrb1<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608483	F	MP:0001413	abnormal response to new environment	Adgrb1<tm2a(EUCOMM)Wtsi>/Adgrb1<tm2a(EUCOMM)Wtsi>	C57BL/6N-Adgrb1<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608483	M	MP:0002079	increased circulating insulin level	Adgrb1<tm2a(EUCOMM)Wtsi>/Adgrb1<tm2a(EUCOMM)Wtsi>	C57BL/6N-Adgrb1<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608483	M	MP:0003019	increased circulating chloride level	Adgrb1<tm2a(EUCOMM)Wtsi>/Adgrb1<tm2a(EUCOMM)Wtsi>	C57BL/6N-Adgrb1<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608484	M	MP:0005562	decreased mean corpuscular hemoglobin	Usp24<tm1a(KOMP)Wtsi>/Usp24<tm1a(KOMP)Wtsi>	C57BL/6N-Usp24<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608484	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Usp24<tm1a(KOMP)Wtsi>/Usp24<tm1a(KOMP)Wtsi>	C57BL/6N-Usp24<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608485	M	MP:0000218	increased leukocyte cell number	Usp21<tm1a(EUCOMM)Wtsi>/Usp21<tm1a(EUCOMM)Wtsi>	C57BL/6N-Usp21<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608486	M	MP:0010067	increased red blood cell distribution width	Elmo1<tm1a(EUCOMM)Wtsi>/Elmo1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Elmo1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608486	M	MP:0003960	increased lean body mass	Elmo1<tm1a(EUCOMM)Wtsi>/Elmo1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Elmo1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608486	M	MP:0013278	decreased fasting circulating glucose level	Elmo1<tm1a(EUCOMM)Wtsi>/Elmo1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Elmo1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608491	M	MP:0010025	decreased total body fat amount	4930591A17Rik<tm1a(KOMP)Wtsi>/4930591A17Rik<tm1a(KOMP)Wtsi>	C57BL/6N-4930591A17Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608491	M	MP:0010123	increased bone mineral content	4930591A17Rik<tm1a(KOMP)Wtsi>/4930591A17Rik<tm1a(KOMP)Wtsi>	C57BL/6N-4930591A17Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608491	M	MP:0010067	increased red blood cell distribution width	4930591A17Rik<tm1a(KOMP)Wtsi>/4930591A17Rik<tm1a(KOMP)Wtsi>	C57BL/6N-4930591A17Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608491	M	MP:0003960	increased lean body mass	4930591A17Rik<tm1a(KOMP)Wtsi>/4930591A17Rik<tm1a(KOMP)Wtsi>	C57BL/6N-4930591A17Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5608494	M	MP:0002098	abnormal vibrissa morphology	Xxylt1<tm1a(EUCOMM)Hmgu>/Xxylt1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Xxylt1<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:5608494	F	MP:0003961	decreased lean body mass	Xxylt1<tm1a(EUCOMM)Hmgu>/Xxylt1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Xxylt1<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:5608590	M	MP:0001458	abnormal object recognition memory	Hprt1<tm1(CAG-Glra3*)Jcme>/Y,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	24430185
MGI:5608590	M	MP:0004494	abnormal synaptic glutamate release	Hprt1<tm1(CAG-Glra3*)Jcme>/Y,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	24430185
MGI:5608590	M	MP:0008414	abnormal spatial reference memory	Hprt1<tm1(CAG-Glra3*)Jcme>/Y,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	24430185
MGI:5608590	M	MP:0002272	abnormal nervous system electrophysiology	Hprt1<tm1(CAG-Glra3*)Jcme>/Y,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	24430185
MGI:5608590	M	MP:0008428	abnormal spatial working memory	Hprt1<tm1(CAG-Glra3*)Jcme>/Y,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	24430185
MGI:5608590	M	MP:0002906	increased susceptibility to pharmacologically induced seizures	Hprt1<tm1(CAG-Glra3*)Jcme>/Y,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	24430185
MGI:5608590	M	MP:0003631	nervous system phenotype	Hprt1<tm1(CAG-Glra3*)Jcme>/Y,Tg(Camk2a-cre)2Gsc/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	Y	24430185
MGI:5608591	M	MP:0002272	abnormal nervous system electrophysiology	Hprt1<tm1(CAG-Glra3*)Jcme>/Y,Pvalb<tm1(cre)Arbr>/Pvalb<+>	involves: 129P2/OlaHsd * C57BL/6J	N	24430185
MGI:5608591	M	MP:0002206	abnormal CNS synaptic transmission	Hprt1<tm1(CAG-Glra3*)Jcme>/Y,Pvalb<tm1(cre)Arbr>/Pvalb<+>	involves: 129P2/OlaHsd * C57BL/6J	N	24430185
MGI:5608591	M	MP:0001363	increased anxiety-related response	Hprt1<tm1(CAG-Glra3*)Jcme>/Y,Pvalb<tm1(cre)Arbr>/Pvalb<+>	involves: 129P2/OlaHsd * C57BL/6J	N	24430185
MGI:5608591	M	MP:0001899	absent long-term depression	Hprt1<tm1(CAG-Glra3*)Jcme>/Y,Pvalb<tm1(cre)Arbr>/Pvalb<+>	involves: 129P2/OlaHsd * C57BL/6J	N	24430185
MGI:5608591	M	MP:0005386	behavior/neurological phenotype	Hprt1<tm1(CAG-Glra3*)Jcme>/Y,Pvalb<tm1(cre)Arbr>/Pvalb<+>	involves: 129P2/OlaHsd * C57BL/6J	Y	24430185
MGI:5608671	F	MP:0001273	decreased metastatic potential	Rhoj<tm1.2Auem>/Rhoj<tm1.2Auem>,Tg(MMTV-PyVT)634Mul/0	involves: C57BL/6 * CBA/JNCrlj * FVB/N	N	24434213
MGI:5608671	F	MP:0010269	decreased mammary gland tumor incidence	Rhoj<tm1.2Auem>/Rhoj<tm1.2Auem>,Tg(MMTV-PyVT)634Mul/0	involves: C57BL/6 * CBA/JNCrlj * FVB/N	N	24434213
MGI:5608671	F	MP:0003447	decreased tumor growth/size	Rhoj<tm1.2Auem>/Rhoj<tm1.2Auem>,Tg(MMTV-PyVT)634Mul/0	involves: C57BL/6 * CBA/JNCrlj * FVB/N	N	24434213
MGI:5608671	F	MP:0010144	abnormal tumor vascularization	Rhoj<tm1.2Auem>/Rhoj<tm1.2Auem>,Tg(MMTV-PyVT)634Mul/0	involves: C57BL/6 * CBA/JNCrlj * FVB/N	N	24434213
MGI:5608791	M	MP:0001153	small seminiferous tubules	Map7<mshi>/Map7<mshi>	B6.CBy-Map7<mshi>/Csu	N	19329343
MGI:5608791	M	MP:0001925	male infertility	Map7<mshi>/Map7<mshi>	B6.CBy-Map7<mshi>/Csu	N	19329343
MGI:5608791	M	MP:0004852	decreased testis weight	Map7<mshi>/Map7<mshi>	B6.CBy-Map7<mshi>/Csu	N	19329343
MGI:5608791	M	MP:0002216	abnormal seminiferous tubule morphology	Map7<mshi>/Map7<mshi>	B6.CBy-Map7<mshi>/Csu	N	19329343
MGI:5608793	M	MP:0004901	decreased male germ cell number	Map7<Gt(ROSABetageo)1Sor>/Map7<mshi>	involves: 129S4/SvJaeSor * BALB/cBy * C57BL/6J	N	19329343
MGI:5608793	M	MP:0004852	decreased testis weight	Map7<Gt(ROSABetageo)1Sor>/Map7<mshi>	involves: 129S4/SvJaeSor * BALB/cBy * C57BL/6J	N	19329343
MGI:5608793	M	MP:0002216	abnormal seminiferous tubule morphology	Map7<Gt(ROSABetageo)1Sor>/Map7<mshi>	involves: 129S4/SvJaeSor * BALB/cBy * C57BL/6J	N	19329343
MGI:5608793	M	MP:0001153	small seminiferous tubules	Map7<Gt(ROSABetageo)1Sor>/Map7<mshi>	involves: 129S4/SvJaeSor * BALB/cBy * C57BL/6J	N	19329343
MGI:5608793	M	MP:0001147	small testis	Map7<Gt(ROSABetageo)1Sor>/Map7<mshi>	involves: 129S4/SvJaeSor * BALB/cBy * C57BL/6J	N	19329343
MGI:5608793	M	MP:0001925	male infertility	Map7<Gt(ROSABetageo)1Sor>/Map7<mshi>	involves: 129S4/SvJaeSor * BALB/cBy * C57BL/6J	N	19329343
MGI:5608896	M	MP:0001147	small testis	Map7<Gt(ROSABetageo)1Sor>/Map7<Gt(ROSABetageo)1Sor>	involves: 129S4/SvJaeSor * C57BL/6J	N	19329343
MGI:5608896	M	MP:0001153	small seminiferous tubules	Map7<Gt(ROSABetageo)1Sor>/Map7<Gt(ROSABetageo)1Sor>	involves: 129S4/SvJaeSor * C57BL/6J	N	19329343
MGI:5608896	M	MP:0002216	abnormal seminiferous tubule morphology	Map7<Gt(ROSABetageo)1Sor>/Map7<Gt(ROSABetageo)1Sor>	involves: 129S4/SvJaeSor * C57BL/6J	N	19329343
MGI:5608896	M	MP:0004852	decreased testis weight	Map7<Gt(ROSABetageo)1Sor>/Map7<Gt(ROSABetageo)1Sor>	involves: 129S4/SvJaeSor * C57BL/6J	N	19329343
MGI:5608896	M	MP:0001925	male infertility	Map7<Gt(ROSABetageo)1Sor>/Map7<Gt(ROSABetageo)1Sor>	involves: 129S4/SvJaeSor * C57BL/6J	N	19329343
MGI:5609257	M	MP:0005344	increased circulating bilirubin level	Abcc2<tm1Ahs>/Abcc2<tm1Ahs>	B6.129P2(FVB)-Abcc2<tm1Ahs>	N	24641901
MGI:5609257	M	MP:0008873	increased physiological sensitivity to xenobiotic	Abcc2<tm1Ahs>/Abcc2<tm1Ahs>	B6.129P2(FVB)-Abcc2<tm1Ahs>	N	24641901
MGI:5609258	M	MP:0005376	homeostasis/metabolism phenotype	Abcc2<tm1.1(ABCC2)Arte>/Abcc2<tm1.1(ABCC2)Arte>	C57BL/6-Abcc2<tm1.1(ABCC2)Arte>	Y	24641901
MGI:5609259	M	MP:0005376	homeostasis/metabolism phenotype	Abcc2<tm1.1(ABCC2)Arte>/Abcc2<tm1.1(ABCC2)Arte>,Nr1i2<tm1(NR1I2)Arte>/Nr1i2<tm1(NR1I2)Arte>	involves: C57BL/6	Y	22917771
MGI:5609276	M	MP:0001556	increased circulating HDL cholesterol level	Kif13b<tm1.1Noh>/Kif13b<tm1.1Noh>	B6.Cg-Kif13b<tm1.1Noh>	N	24469637
MGI:5609276	M	MP:0012329	increased circulating factor VIII level	Kif13b<tm1.1Noh>/Kif13b<tm1.1Noh>	B6.Cg-Kif13b<tm1.1Noh>	N	24469637
MGI:5609276	M	MP:0005178	increased circulating cholesterol level	Kif13b<tm1.1Noh>/Kif13b<tm1.1Noh>	B6.Cg-Kif13b<tm1.1Noh>	N	24469637
MGI:5609276	M	MP:0000182	increased circulating LDL cholesterol level	Kif13b<tm1.1Noh>/Kif13b<tm1.1Noh>	B6.Cg-Kif13b<tm1.1Noh>	N	24469637
MGI:5609309	M	MP:0001925	male infertility	Dnaaf6rt<tm1.2Hmd>/Dnaaf6rt<tm1.2Hmd>	involves: ICR	N	24421334
MGI:5609309	M	MP:0002675	asthenozoospermia	Dnaaf6rt<tm1.2Hmd>/Dnaaf6rt<tm1.2Hmd>	involves: ICR	N	24421334
MGI:5609309	M	MP:0005389	reproductive system phenotype	Dnaaf6rt<tm1.2Hmd>/Dnaaf6rt<tm1.2Hmd>	involves: ICR	Y	24421334
MGI:5609309	M	MP:0009239	short sperm flagellum	Dnaaf6rt<tm1.2Hmd>/Dnaaf6rt<tm1.2Hmd>	involves: ICR	N	24421334
MGI:5609309	M	MP:0009838	abnormal sperm axoneme morphology	Dnaaf6rt<tm1.2Hmd>/Dnaaf6rt<tm1.2Hmd>	involves: ICR	N	24421334
MGI:5609309	M	MP:0003698	abnormal male reproductive system physiology	Dnaaf6rt<tm1.2Hmd>/Dnaaf6rt<tm1.2Hmd>	involves: ICR	N	24421334
MGI:5609309	M	MP:0009242	thin sperm flagellum	Dnaaf6rt<tm1.2Hmd>/Dnaaf6rt<tm1.2Hmd>	involves: ICR	N	24421334
MGI:5609309	M	MP:0008892	abnormal sperm flagellum morphology	Dnaaf6rt<tm1.2Hmd>/Dnaaf6rt<tm1.2Hmd>	involves: ICR	N	24421334
MGI:5609864	M	MP:0001925	male infertility	Spaca6<Tg(Tyr)Bart97bCeb>/Spaca6<Tg(Tyr)Bart97bCeb>	FVB/N-Spaca6<Tg(Tyr)Bart97bCeb>	N	24275887
MGI:5610007	M	MP:0001922	reduced male fertility	Igh<tm1(IGH)Vlcg>/Igh<tm1(IGH)Vlcg>	involves: 129S6/SvEvTac * C57BL/6N	N	24706858
MGI:5610008	M	MP:0001922	reduced male fertility	Igh<tm1(IGH)Vlcg>/Igh<tm1(IGH)Vlcg>,Igk<tm1(IGK)Vlcg>/Igk<tm1(IGK)Vlcg>	involves: 129S6/SvEvTac * C57BL/6N	N	24706858
MGI:5610009	M	MP:0001922	reduced male fertility	Igh<tm2(IGH)Vlcg>/Igh<tm2(IGH)Vlcg>	involves: 129S6/SvEvTac * C57BL/6N	N	24706858
MGI:5610010	M	MP:0001922	reduced male fertility	Igh<tm2(IGH)Vlcg>/Igh<tm2(IGH)Vlcg>,Igk<tm2(IGK)Vlcg>/Igk<tm2(IGK)Vlcg>	involves: 129S6/SvEvTac * C57BL/6N	N	24706858
MGI:5610011	M	MP:0001922	reduced male fertility	Igh<tm3.1(IGH)Vlcg>/Igh<tm3.1(IGH)Vlcg>	involves: 129S6/SvEvTac * C57BL/6N	N	24706858
MGI:5610012	M	MP:0001922	reduced male fertility	Igh<tm3.1(IGH)Vlcg>/Igh<tm3.1(IGH)Vlcg>,Igk<tm3.1(IGK)Vlcg>/Igk<tm3.1(IGK)Vlcg>	involves: 129S6/SvEvTac * C57BL/6N	N	24706858
MGI:5610133	F	MP:0004021	abnormal rod electrophysiology	Rpgr<tm1.1Sgj>/Rpgr<tm1.1Sgj>	involves: 129 * BALB/c	N	22807293
MGI:5610133	F	MP:0008515	thin retina outer nuclear layer	Rpgr<tm1.1Sgj>/Rpgr<tm1.1Sgj>	involves: 129 * BALB/c	N	22807293
MGI:5610133	F	MP:0004022	abnormal cone electrophysiology	Rpgr<tm1.1Sgj>/Rpgr<tm1.1Sgj>	involves: 129 * BALB/c	N	22807293
MGI:5610133	F	MP:0001326	retina degeneration	Rpgr<tm1.1Sgj>/Rpgr<tm1.1Sgj>	involves: 129 * BALB/c	N	22807293
MGI:5610134	M	MP:0001326	retina degeneration	Rpgr<tm1.1Sgj>/Y	involves: 129 * BALB/c	N	22807293
MGI:5610134	M	MP:0004022	abnormal cone electrophysiology	Rpgr<tm1.1Sgj>/Y	involves: 129 * BALB/c	N	22807293
MGI:5610134	M	MP:0004021	abnormal rod electrophysiology	Rpgr<tm1.1Sgj>/Y	involves: 129 * BALB/c	N	22807293
MGI:5610134	M	MP:0008515	thin retina outer nuclear layer	Rpgr<tm1.1Sgj>/Y	involves: 129 * BALB/c	N	22807293
MGI:5610137	F	MP:0013475	delayed reproductive senescence	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5610137	F	MP:0009006	prolonged estrous cycle	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5610137	F	MP:0003699	abnormal female reproductive system physiology	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5610137	F	MP:0006043	decreased apoptosis	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5610137	F	MP:0001125	abnormal oocyte morphology	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5610137	F	MP:0011128	increased tertiary ovarian follicle number	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5610137	F	MP:0031421	increased superovulation rate	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5610137	F	MP:0009017	prolonged estrus	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5610137	F	MP:0031383	increased secondary ovarian follicle number	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5610137	F	MP:0011120	increased primordial ovarian follicle number	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5610137	F	MP:0009083	uterus hypertrophy	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5610137	F	MP:0011124	increased primary ovarian follicle number	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5610137	F	MP:0001130	abnormal ovarian folliculogenesis	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5610137	F	MP:0008871	abnormal ovarian follicle number	Eef2k<tm1Agry>/Eef2k<tm1Agry>	B6.Cg-Eef2k<tm1Agry>	N	24582807
MGI:5613396	M	MP:0003383	abnormal gluconeogenesis	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0005376	homeostasis/metabolism phenotype	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	Y	21966465
MGI:5613396	M	MP:0009171	enlarged pancreatic islets	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0001556	increased circulating HDL cholesterol level	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0001547	abnormal lipid level	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0003059	decreased insulin secretion	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0005386	behavior/neurological phenotype	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	Y	21966465
MGI:5613396	M	MP:0031269	increased susceptibility to diet-induced hepatic steatosis	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0005659	decreased susceptibility to diet-induced obesity	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0000186	decreased circulating HDL cholesterol level	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0009133	decreased white fat cell size	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0031415	increased skeletal muscle triglyceride level	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0013373	increased sebum secretion	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0001559	hyperglycemia	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0010378	increased respiratory quotient	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0002078	abnormal glucose homeostasis	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0000182	increased circulating LDL cholesterol level	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0009355	increased liver triglyceride level	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0005293	impaired glucose tolerance	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0005145	increased circulating VLDL cholesterol level	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0001262	decreased body weight	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0001554	increased circulating free fatty acids level	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0003976	decreased circulating VLDL triglyceride level	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0001552	increased circulating triglyceride level	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0005178	increased circulating cholesterol level	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0020477	abnormal locomotor circadian rhythm	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0002727	decreased circulating insulin level	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613396	M	MP:0010025	decreased total body fat amount	Bmal1<tm1.2Shbi>/Bmal1<tm1.2Shbi>	involves: C57BL/6J	N	21966465
MGI:5613900	M	MP:0001932	abnormal spermiogenesis	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5613900	M	MP:0001925	male infertility	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5613900	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5613900	M	MP:0002675	asthenozoospermia	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5613900	M	MP:0009833	absent sperm mitochondrial sheath	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5613900	M	MP:0006380	abnormal spermatid morphology	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5613900	M	MP:0000242	impaired fertilization	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5613900	M	MP:0008898	abnormal acrosome morphology	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5613900	M	MP:0009852	increased Sertoli cell phagocytosis	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5613900	M	MP:0009230	abnormal sperm head morphology	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5613900	M	MP:0002687	oligozoospermia	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5613900	M	MP:0005578	teratozoospermia	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5613900	M	MP:0008280	abnormal male germ cell apoptosis	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5613900	M	MP:0002686	globozoospermia	Osbp2<tm1Arai>/Osbp2<tm1Arai>	C57BL/6-Osbp2<tm1Arai>	N	24245814
MGI:5614073	M	MP:0002216	abnormal seminiferous tubule morphology	Rad50<tm4.1Jpt>/Rad50<+>	involves: 129/Sv * C57BL/6	N	24532689
MGI:5614073	F	MP:0001926	female infertility	Rad50<tm4.1Jpt>/Rad50<+>	involves: 129/Sv * C57BL/6	N	24532689
MGI:5614073	M	MP:0003205	testicular atrophy	Rad50<tm4.1Jpt>/Rad50<+>	involves: 129/Sv * C57BL/6	N	24532689
MGI:5614073	F	MP:0001923	reduced female fertility	Rad50<tm4.1Jpt>/Rad50<+>	involves: 129/Sv * C57BL/6	N	24532689
MGI:5614073	F	MP:0001935	decreased litter size	Rad50<tm4.1Jpt>/Rad50<+>	involves: 129/Sv * C57BL/6	N	24532689
MGI:5614073	F	MP:0004833	ovary atrophy	Rad50<tm4.1Jpt>/Rad50<+>	involves: 129/Sv * C57BL/6	N	24532689
MGI:5614073	M	MP:0001929	abnormal gametogenesis	Rad50<tm4.1Jpt>/Rad50<+>	involves: 129/Sv * C57BL/6	N	24532689
MGI:5614073	M	MP:0001147	small testis	Rad50<tm4.1Jpt>/Rad50<+>	involves: 129/Sv * C57BL/6	N	24532689
MGI:5614073	M	MP:0001925	male infertility	Rad50<tm4.1Jpt>/Rad50<+>	involves: 129/Sv * C57BL/6	N	24532689
MGI:5614073	M	MP:0001156	abnormal spermatogenesis	Rad50<tm4.1Jpt>/Rad50<+>	involves: 129/Sv * C57BL/6	N	24532689
MGI:5614073	M	MP:0002673	abnormal sperm number	Rad50<tm4.1Jpt>/Rad50<+>	involves: 129/Sv * C57BL/6	N	24532689
MGI:5614080	M	MP:0002216	abnormal seminiferous tubule morphology	Rad50<tm4.1Jpt>/Rad50<+>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129/Sv * C57BL/6	N	24532689
MGI:5614309	M	MP:0002995	primary sex reversal	Fgfr2<hob>/Fgfr2<hob>	involves: C57BL/6J	N	24956260
MGI:5614321	M	MP:0002995	primary sex reversal	Fgfr2<tm1.1Dor>/Fgfr2<hob>	involves: 129X1/SvJ * C57BL/6J * FVB/N	N	24956260
MGI:5614325	M	MP:0011799	increased urinary bladder weight	Cavin1<tm1Pfp>/Cavin1<tm1Pfp>	B6.129S6-Cavin1<tm1Pfp>/J	N	22643325
MGI:5614553	M	MP:0008489	slow postnatal weight gain	Scn4a<m1Aaa>/Scn4a<+>	involves: BALB/c * C57BL/6J	N	25348630
MGI:5615442	F	MP:0001926	female infertility	Tshb<tm1Hru>/Tshb<tm1Hru>	CBA.Cg-Tshb<tm1Hru>	N	23758111
MGI:5615442	M	MP:0001925	male infertility	Tshb<tm1Hru>/Tshb<tm1Hru>	CBA.Cg-Tshb<tm1Hru>	N	23758111
MGI:5615459	M	MP:0003205	testicular atrophy	Siglech<tm1.1Cfg>/Siglech<tm1.1Cfg>	involves: C57BL/6	N	23118208
MGI:5615459	M	MP:0002216	abnormal seminiferous tubule morphology	Siglech<tm1.1Cfg>/Siglech<tm1.1Cfg>	involves: C57BL/6	N	23118208
MGI:5615472	M	MP:0005169	abnormal male meiosis	Smad4<tm2.1Cxd>/Smad4<tm2.1Cxd>,Tg(Pou5f1-cre/ERT2)#Ysa/0	involves: 129S6/SvEvTac	N	23221368
MGI:5615600	M	MP:0001154	seminiferous tubule degeneration	Clec4a2<tm1.1Cfg>/Clec4a2<tm1.1Cfg>	involves: C57BL/6	N	23118208
MGI:5615634	F	MP:0001130	abnormal ovarian folliculogenesis	Chst3<tm1Tmu>/Chst3<tm1Tmu>	involves: 129S2/SvPas	N	23118208
MGI:5615704	M	MP:0009451	abnormal chromosomal synapsis	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac * C57BL/6J	N	24589552
MGI:5615704	M	MP:0005169	abnormal male meiosis	Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac * C57BL/6J	N	24589552
MGI:5615708	M	MP:0004852	decreased testis weight	Rad21l<tm1Yow>/Rad21l<tm1Yow>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615708	M	MP:0005169	abnormal male meiosis	Rad21l<tm1Yow>/Rad21l<tm1Yow>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615708	M	MP:0001925	male infertility	Rad21l<tm1Yow>/Rad21l<tm1Yow>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615708	M	MP:0009451	abnormal chromosomal synapsis	Rad21l<tm1Yow>/Rad21l<tm1Yow>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615708	F	MP:0005168	abnormal female meiosis	Rad21l<tm1Yow>/Rad21l<tm1Yow>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615708	M	MP:0008261	arrest of male meiosis	Rad21l<tm1Yow>/Rad21l<tm1Yow>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615708	M	MP:0001147	small testis	Rad21l<tm1Yow>/Rad21l<tm1Yow>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615708	M	MP:0009452	abnormal synaptonemal complex	Rad21l<tm1Yow>/Rad21l<tm1Yow>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615708	F	MP:0002777	absent ovarian follicles	Rad21l<tm1Yow>/Rad21l<tm1Yow>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615708	F	MP:0004805	absent oocytes	Rad21l<tm1Yow>/Rad21l<tm1Yow>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615708	F	MP:0001926	female infertility	Rad21l<tm1Yow>/Rad21l<tm1Yow>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615722	M	MP:0005169	abnormal male meiosis	Rad21l<tm1Yow>/Rad21l<tm1Yow>,Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615728	M	MP:0005169	abnormal male meiosis	Rec8<mei8>/Rec8<mei8>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	24589552
MGI:5615728	M	MP:0009452	abnormal synaptonemal complex	Rec8<mei8>/Rec8<mei8>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	24589552
MGI:5615730	M	MP:0009451	abnormal chromosomal synapsis	Rad21l<tm1Yow>/Rad21l<tm1Yow>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615730	M	MP:0009452	abnormal synaptonemal complex	Rad21l<tm1Yow>/Rad21l<tm1Yow>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615730	M	MP:0005169	abnormal male meiosis	Rad21l<tm1Yow>/Rad21l<tm1Yow>,Spo11<tm1Mjn>/Spo11<tm1Mjn>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615731	M	MP:0009451	abnormal chromosomal synapsis	Rad21l<tm1Yow>/Rad21l<tm1Yow>,Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5615731	M	MP:0005169	abnormal male meiosis	Rad21l<tm1Yow>/Rad21l<tm1Yow>,Sun1<tm1Mhan>/Sun1<tm1Mhan>	involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24589552
MGI:5616633	M	MP:0002206	abnormal CNS synaptic transmission	Mbnl2<tm1.1Sws>/Mbnl2<tm1.1Sws>	involves: 129S1/SvImJ * BALB/cJ * C57BL/6J	N	22884328
MGI:5616633	M	MP:0001900	impaired synaptic plasticity	Mbnl2<tm1.1Sws>/Mbnl2<tm1.1Sws>	involves: 129S1/SvImJ * BALB/cJ * C57BL/6J	N	22884328
MGI:5616633	M	MP:0001473	reduced long-term potentiation	Mbnl2<tm1.1Sws>/Mbnl2<tm1.1Sws>	involves: 129S1/SvImJ * BALB/cJ * C57BL/6J	N	22884328
MGI:5616633	M	MP:0011086	postnatal lethality, incomplete penetrance	Mbnl2<tm1.1Sws>/Mbnl2<tm1.1Sws>	involves: 129S1/SvImJ * BALB/cJ * C57BL/6J	N	22884328
MGI:5616633	M	MP:0009436	fragmentation of sleep/wake states	Mbnl2<tm1.1Sws>/Mbnl2<tm1.1Sws>	involves: 129S1/SvImJ * BALB/cJ * C57BL/6J	N	22884328
MGI:5616633	M	MP:0002912	abnormal excitatory postsynaptic potential	Mbnl2<tm1.1Sws>/Mbnl2<tm1.1Sws>	involves: 129S1/SvImJ * BALB/cJ * C57BL/6J	N	22884328
MGI:5616633	M	MP:0003997	tonic-clonic seizures	Mbnl2<tm1.1Sws>/Mbnl2<tm1.1Sws>	involves: 129S1/SvImJ * BALB/cJ * C57BL/6J	N	22884328
MGI:5616633	M	MP:0012287	increased frequency of paradoxical sleep	Mbnl2<tm1.1Sws>/Mbnl2<tm1.1Sws>	involves: 129S1/SvImJ * BALB/cJ * C57BL/6J	N	22884328
MGI:5616633	M	MP:0012288	abnormal paradoxical sleep pattern	Mbnl2<tm1.1Sws>/Mbnl2<tm1.1Sws>	involves: 129S1/SvImJ * BALB/cJ * C57BL/6J	N	22884328
MGI:5616651	M	MP:0002906	increased susceptibility to pharmacologically induced seizures	Mbnl2<tm1.1Sws>/Mbnl2<+>	involves: 129S1/SvImJ * BALB/cJ * C57BL/6J	N	22884328
MGI:5617031	M	MP:0001925	male infertility	Sptbn4<qv>/Sptbn4<qv>	either: (involves: BALB/c) or (involves: C57BL/10)	N	MGI:48707
MGI:5617140	F	MP:0002680	decreased corpora lutea number	Fmr1<tm1Usdn>/Fmr1<tm1Usdn>	B6.129S6(Cg)-Fmr1<tm1Usdn>	N	22470123
MGI:5617140	F	MP:0031239	increased atretic ovarian follicle number	Fmr1<tm1Usdn>/Fmr1<tm1Usdn>	B6.129S6(Cg)-Fmr1<tm1Usdn>	N	22470123
MGI:5617140	F	MP:0004833	ovary atrophy	Fmr1<tm1Usdn>/Fmr1<tm1Usdn>	B6.129S6(Cg)-Fmr1<tm1Usdn>	N	22470123
MGI:5617140	F	MP:0001127	small ovary	Fmr1<tm1Usdn>/Fmr1<tm1Usdn>	B6.129S6(Cg)-Fmr1<tm1Usdn>	N	22470123
MGI:5617140	F	MP:0001126	abnormal ovary morphology	Fmr1<tm1Usdn>/Fmr1<tm1Usdn>	B6.129S6(Cg)-Fmr1<tm1Usdn>	N	22470123
MGI:5617140	F	MP:0006361	abnormal female germ cell morphology	Fmr1<tm1Usdn>/Fmr1<tm1Usdn>	B6.129S6(Cg)-Fmr1<tm1Usdn>	N	22470123
MGI:5617140	F	MP:0005168	abnormal female meiosis	Fmr1<tm1Usdn>/Fmr1<tm1Usdn>	B6.129S6(Cg)-Fmr1<tm1Usdn>	N	22470123
MGI:5617140	F	MP:0002016	ovary cyst	Fmr1<tm1Usdn>/Fmr1<tm1Usdn>	B6.129S6(Cg)-Fmr1<tm1Usdn>	N	22470123
MGI:5617140	F	MP:0009372	abnormal cumulus oophorus morphology	Fmr1<tm1Usdn>/Fmr1<tm1Usdn>	B6.129S6(Cg)-Fmr1<tm1Usdn>	N	22470123
MGI:5617140	F	MP:0009363	abnormal tertiary ovarian follicle morphology	Fmr1<tm1Usdn>/Fmr1<tm1Usdn>	B6.129S6(Cg)-Fmr1<tm1Usdn>	N	22470123
MGI:5617140	F	MP:0008868	abnormal granulosa cell morphology	Fmr1<tm1Usdn>/Fmr1<tm1Usdn>	B6.129S6(Cg)-Fmr1<tm1Usdn>	N	22470123
MGI:5617140	F	MP:0008871	abnormal ovarian follicle number	Fmr1<tm1Usdn>/Fmr1<tm1Usdn>	B6.129S6(Cg)-Fmr1<tm1Usdn>	N	22470123
MGI:5617468	M	MP:0003461	abnormal response to novel object	Mbd5<Gt(Ayu21-B205)Imeg>/Mbd5<+>	B6.Cg-Mbd5<Gt(Ayu21-B205)Imeg>	N	25001218
MGI:5617468	M	MP:0002066	abnormal motor capabilities/coordination/movement	Mbd5<Gt(Ayu21-B205)Imeg>/Mbd5<+>	B6.Cg-Mbd5<Gt(Ayu21-B205)Imeg>	N	25001218
MGI:5617468	M	MP:0005386	behavior/neurological phenotype	Mbd5<Gt(Ayu21-B205)Imeg>/Mbd5<+>	B6.Cg-Mbd5<Gt(Ayu21-B205)Imeg>	Y	25001218
MGI:5617468	M	MP:0001441	increased grooming behavior	Mbd5<Gt(Ayu21-B205)Imeg>/Mbd5<+>	B6.Cg-Mbd5<Gt(Ayu21-B205)Imeg>	N	25001218
MGI:5617468	M	MP:0001360	abnormal social investigation	Mbd5<Gt(Ayu21-B205)Imeg>/Mbd5<+>	B6.Cg-Mbd5<Gt(Ayu21-B205)Imeg>	N	25001218
MGI:5617468	M	MP:0001405	impaired coordination	Mbd5<Gt(Ayu21-B205)Imeg>/Mbd5<+>	B6.Cg-Mbd5<Gt(Ayu21-B205)Imeg>	N	25001218
MGI:5617468	M	MP:0010053	decreased grip strength	Mbd5<Gt(Ayu21-B205)Imeg>/Mbd5<+>	B6.Cg-Mbd5<Gt(Ayu21-B205)Imeg>	N	25001218
MGI:5617468	M	MP:0002063	abnormal learning/memory/conditioning	Mbd5<Gt(Ayu21-B205)Imeg>/Mbd5<+>	B6.Cg-Mbd5<Gt(Ayu21-B205)Imeg>	N	25001218
MGI:5617484	M	MP:0005289	increased oxygen consumption	Timp3<tm1Osya>/Timp3<tm1Osya>	involves: 129P2/OlaHsd * C57BL/6J	N	24736588
MGI:5617484	M	MP:0005533	increased body temperature	Timp3<tm1Osya>/Timp3<tm1Osya>	involves: 129P2/OlaHsd * C57BL/6J	N	24736588
MGI:5617484	M	MP:0008963	increased carbon dioxide production	Timp3<tm1Osya>/Timp3<tm1Osya>	involves: 129P2/OlaHsd * C57BL/6J	N	24736588
MGI:5617484	M	MP:0020523	decreased susceptibility to induced hypothermia	Timp3<tm1Osya>/Timp3<tm1Osya>	involves: 129P2/OlaHsd * C57BL/6J	N	24736588
MGI:5617493	F	MP:0001126	abnormal ovary morphology	Tg(Krt18-EGFP,-TAg121)36Ysng/0	involves: C57BL/6 * DBA/2	N	22617326
MGI:5617493	F	MP:0008000	increased ovary tumor incidence	Tg(Krt18-EGFP,-TAg121)36Ysng/0	involves: C57BL/6 * DBA/2	N	22617326
MGI:5617493	F	MP:0003579	increased ovarian carcinoma incidence	Tg(Krt18-EGFP,-TAg121)36Ysng/0	involves: C57BL/6 * DBA/2	N	22617326
MGI:5617493	F	MP:0001128	ovary hyperplasia	Tg(Krt18-EGFP,-TAg121)36Ysng/0	involves: C57BL/6 * DBA/2	N	22617326
MGI:5617494	F	MP:0008000	increased ovary tumor incidence	Tg(Krt18-EGFP,-TAg121)36Ysng/0,Trp53<tm1Brn>/Trp53<tm2Tyj>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	N	22617326
MGI:5617495	F	MP:0008000	increased ovary tumor incidence	Tg(Krt18-EGFP,-TAg121)36Ysng/0,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * FVB/N	N	22617326
MGI:5617496	F	MP:0002038	increased carcinoma incidence	Brca1<tm1Brn>/Brca1<tm1Brn>,Tg(Krt18-EGFP,-TAg121)36Ysng/0,Trp53<tm1Brn>/Trp53<tm2Tyj>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	N	22617326
MGI:5617496	F	MP:0013184	hemorrhagic ascites	Brca1<tm1Brn>/Brca1<tm1Brn>,Tg(Krt18-EGFP,-TAg121)36Ysng/0,Trp53<tm1Brn>/Trp53<tm2Tyj>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	N	22617326
MGI:5617496	F	MP:0008000	increased ovary tumor incidence	Brca1<tm1Brn>/Brca1<tm1Brn>,Tg(Krt18-EGFP,-TAg121)36Ysng/0,Trp53<tm1Brn>/Trp53<tm2Tyj>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	N	22617326
MGI:5617496	F	MP:0003574	abnormal oviduct morphology	Brca1<tm1Brn>/Brca1<tm1Brn>,Tg(Krt18-EGFP,-TAg121)36Ysng/0,Trp53<tm1Brn>/Trp53<tm2Tyj>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	N	22617326
MGI:5617496	F	MP:0001272	increased metastatic potential	Brca1<tm1Brn>/Brca1<tm1Brn>,Tg(Krt18-EGFP,-TAg121)36Ysng/0,Trp53<tm1Brn>/Trp53<tm2Tyj>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	N	22617326
MGI:5617496	F	MP:0003579	increased ovarian carcinoma incidence	Brca1<tm1Brn>/Brca1<tm1Brn>,Tg(Krt18-EGFP,-TAg121)36Ysng/0,Trp53<tm1Brn>/Trp53<tm2Tyj>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	N	22617326
MGI:5617497	F	MP:0008000	increased ovary tumor incidence	Brca2<tm1Brn>/Brca2<tm1Brn>,Tg(Krt18-EGFP,-TAg121)36Ysng/0,Trp53<tm1Brn>/Trp53<tm2Tyj>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	N	22617326
MGI:5617499	F	MP:0008000	increased ovary tumor incidence	Brca1<tm1Brn>/Brca1<tm1Brn>,Tg(Krt18-EGFP,-TAg121)36Ysng/0,Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * FVB/N	N	22617326
MGI:5617525	F	MP:0005397	hematopoietic system phenotype	Heph<sla>/Heph<+>	Not Specified	Y	MGI:4415729
MGI:5617540	M	MP:0001925	male infertility	Ggt1<enu1>/Ggt1<enu1>	C57BL/6J-Ggt1<enu1>	N	9139708
MGI:5617540	F	MP:0001926	female infertility	Ggt1<enu1>/Ggt1<enu1>	C57BL/6J-Ggt1<enu1>	N	9139708
MGI:5617753	M	MP:0004924	abnormal behavior	Tg(Camk2a-Bdnf)A9Stl/0	C57BL/6-Tg(Camk2a-Bdnf)A9Stl/J	N	24768643
MGI:5617753	M	MP:0001262	decreased body weight	Tg(Camk2a-Bdnf)A9Stl/0	C57BL/6-Tg(Camk2a-Bdnf)A9Stl/J	N	24768643
MGI:5617753	M	MP:0002195	psychomotor seizures	Tg(Camk2a-Bdnf)A9Stl/0	C57BL/6-Tg(Camk2a-Bdnf)A9Stl/J	N	24768643
MGI:5617753	M	MP:0001364	decreased anxiety-related response	Tg(Camk2a-Bdnf)A9Stl/0	C57BL/6-Tg(Camk2a-Bdnf)A9Stl/J	N	24768643
MGI:5617753	M	MP:0002064	seizures	Tg(Camk2a-Bdnf)A9Stl/0	C57BL/6-Tg(Camk2a-Bdnf)A9Stl/J	N	24768643
MGI:5618132	M	MP:0005165	increased susceptibility to injury	Casp8<tm1Clie>/Casp8<tm1Clie>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618132	M	MP:0001570	abnormal circulating enzyme level	Casp8<tm1Clie>/Casp8<tm1Clie>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618132	M	MP:0005166	decreased susceptibility to injury	Casp8<tm1Clie>/Casp8<tm1Clie>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618132	M	MP:0001860	liver inflammation	Casp8<tm1Clie>/Casp8<tm1Clie>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618136	M	MP:0001265	decreased body size	Casp8<tm1Clie>/Casp8<tm1Clie>,Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618136	M	MP:0005415	intrahepatic cholestasis	Casp8<tm1Clie>/Casp8<tm1Clie>,Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618136	M	MP:0000599	enlarged liver	Casp8<tm1Clie>/Casp8<tm1Clie>,Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618136	M	MP:0003333	liver fibrosis	Casp8<tm1Clie>/Casp8<tm1Clie>,Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618136	M	MP:0000598	abnormal liver morphology	Casp8<tm1Clie>/Casp8<tm1Clie>,Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618136	M	MP:0004789	increased bile salt level	Casp8<tm1Clie>/Casp8<tm1Clie>,Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618136	M	MP:0005344	increased circulating bilirubin level	Casp8<tm1Clie>/Casp8<tm1Clie>,Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618136	M	MP:0002006	neoplasm	Casp8<tm1Clie>/Casp8<tm1Clie>,Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	Y	21878202
MGI:5618136	M	MP:0005083	abnormal biliary tract morphology	Casp8<tm1Clie>/Casp8<tm1Clie>,Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618136	M	MP:0001654	hepatic necrosis	Casp8<tm1Clie>/Casp8<tm1Clie>,Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618136	M	MP:0001570	abnormal circulating enzyme level	Casp8<tm1Clie>/Casp8<tm1Clie>,Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5618136	M	MP:0002968	increased circulating alkaline phosphatase level	Casp8<tm1Clie>/Casp8<tm1Clie>,Ikbkg<tm1.1Chtr>/Ikbkg<tm1.1Chtr>,Tg(Alb1-cre)7Gsc/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	21878202
MGI:5619363	F	MP:0012143	decreased a-wave amplitude	Rp2<tm1.2Asw>/Rp2<tm1.2Asw>	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5619363	F	MP:0004022	abnormal cone electrophysiology	Rp2<tm1.2Asw>/Rp2<tm1.2Asw>	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5619363	F	MP:0001004	abnormal retina photoreceptor morphology	Rp2<tm1.2Asw>/Rp2<tm1.2Asw>	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5619363	F	MP:0008515	thin retina outer nuclear layer	Rp2<tm1.2Asw>/Rp2<tm1.2Asw>	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5619363	F	MP:0008586	disorganized photoreceptor outer segment	Rp2<tm1.2Asw>/Rp2<tm1.2Asw>	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5619363	F	MP:0004021	abnormal rod electrophysiology	Rp2<tm1.2Asw>/Rp2<tm1.2Asw>	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5619363	F	MP:0012144	decreased b-wave amplitude	Rp2<tm1.2Asw>/Rp2<tm1.2Asw>	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5619363	F	MP:0005391	vision/eye phenotype	Rp2<tm1.2Asw>/Rp2<tm1.2Asw>	involves: 129S/SvEv * C57BL/6	Y	23745007
MGI:5619363	F	MP:0008446	decreased retina cone cell number	Rp2<tm1.2Asw>/Rp2<tm1.2Asw>	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5619600	F	MP:0004905	decreased uterus weight	Kdm5b<Gt(RRO123)Byg>/Kdm5b<Gt(RRO123)Byg>	FVB.129P2-Kdm5b<Gt(RRO123)Byg>	N	24802759
MGI:5619600	F	MP:0001923	reduced female fertility	Kdm5b<Gt(RRO123)Byg>/Kdm5b<Gt(RRO123)Byg>	FVB.129P2-Kdm5b<Gt(RRO123)Byg>	N	24802759
MGI:5619600	F	MP:0000628	abnormal mammary gland development	Kdm5b<Gt(RRO123)Byg>/Kdm5b<Gt(RRO123)Byg>	FVB.129P2-Kdm5b<Gt(RRO123)Byg>	N	24802759
MGI:5619600	F	MP:0001926	female infertility	Kdm5b<Gt(RRO123)Byg>/Kdm5b<Gt(RRO123)Byg>	FVB.129P2-Kdm5b<Gt(RRO123)Byg>	N	24802759
MGI:5619600	F	MP:0005181	decreased circulating estradiol level	Kdm5b<Gt(RRO123)Byg>/Kdm5b<Gt(RRO123)Byg>	FVB.129P2-Kdm5b<Gt(RRO123)Byg>	N	24802759
MGI:5619600	F	MP:0000662	abnormal branching of the mammary ductal tree	Kdm5b<Gt(RRO123)Byg>/Kdm5b<Gt(RRO123)Byg>	FVB.129P2-Kdm5b<Gt(RRO123)Byg>	N	24802759
MGI:5620009	M	MP:0002059	abnormal seminal vesicle morphology	Fgfr2<svs>/Fgfr2<svs>	either: CXB1/By or CXB1/ByEss * CXB1/ByLac	N	3181757
MGI:5620202	M	MP:0001925	male infertility	Snai2<tm2Grid>/Snai2<tm2Grid>,Snai3<tm1.2Jhws>/Snai3<tm1.2Jhws>	involves: 129/Sv * 129S1/Sv * C57BL/6	N	23874916
MGI:5620352	M	MP:0004022	abnormal cone electrophysiology	Rp2<tm1.2Asw>/Y	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5620352	M	MP:0001004	abnormal retina photoreceptor morphology	Rp2<tm1.2Asw>/Y	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5620352	M	MP:0012143	decreased a-wave amplitude	Rp2<tm1.2Asw>/Y	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5620352	M	MP:0012144	decreased b-wave amplitude	Rp2<tm1.2Asw>/Y	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5620352	M	MP:0004021	abnormal rod electrophysiology	Rp2<tm1.2Asw>/Y	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5620352	M	MP:0008586	disorganized photoreceptor outer segment	Rp2<tm1.2Asw>/Y	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5620352	M	MP:0008515	thin retina outer nuclear layer	Rp2<tm1.2Asw>/Y	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5620352	M	MP:0008446	decreased retina cone cell number	Rp2<tm1.2Asw>/Y	involves: 129S/SvEv * C57BL/6	N	23745007
MGI:5620352	M	MP:0005391	vision/eye phenotype	Rp2<tm1.2Asw>/Y	involves: 129S/SvEv * C57BL/6	Y	23745007
MGI:5620462	M	MP:0009230	abnormal sperm head morphology	Rapgef6<tm1.1Tkat>/Rapgef6<tm1.1Tkat>	involves: 129P2/OlaHsd	N	24491570
MGI:5620462	M	MP:0002216	abnormal seminiferous tubule morphology	Rapgef6<tm1.1Tkat>/Rapgef6<tm1.1Tkat>	involves: 129P2/OlaHsd	N	24491570
MGI:5620462	M	MP:0003205	testicular atrophy	Rapgef6<tm1.1Tkat>/Rapgef6<tm1.1Tkat>	involves: 129P2/OlaHsd	N	24491570
MGI:5620462	M	MP:0001922	reduced male fertility	Rapgef6<tm1.1Tkat>/Rapgef6<tm1.1Tkat>	involves: 129P2/OlaHsd	N	24491570
MGI:5620462	M	MP:0001156	abnormal spermatogenesis	Rapgef6<tm1.1Tkat>/Rapgef6<tm1.1Tkat>	involves: 129P2/OlaHsd	N	24491570
MGI:5620462	M	MP:0000691	enlarged spleen	Rapgef6<tm1.1Tkat>/Rapgef6<tm1.1Tkat>	involves: 129P2/OlaHsd	N	24491570
MGI:5620462	M	MP:0005376	homeostasis/metabolism phenotype	Rapgef6<tm1.1Tkat>/Rapgef6<tm1.1Tkat>	involves: 129P2/OlaHsd	Y	24491570
MGI:5620462	M	MP:0002675	asthenozoospermia	Rapgef6<tm1.1Tkat>/Rapgef6<tm1.1Tkat>	involves: 129P2/OlaHsd	N	24491570
MGI:5620462	M	MP:0001147	small testis	Rapgef6<tm1.1Tkat>/Rapgef6<tm1.1Tkat>	involves: 129P2/OlaHsd	N	24491570
MGI:5620462	M	MP:0002687	oligozoospermia	Rapgef6<tm1.1Tkat>/Rapgef6<tm1.1Tkat>	involves: 129P2/OlaHsd	N	24491570
MGI:5620503	F	MP:0003633	abnormal nervous system physiology	Gnao1<tm2.1Rneu>/Gnao1<+>	B6.129S-Gnao1<tm2.1Rneu>	N	24700286
MGI:5620504	F	MP:0005386	behavior/neurological phenotype	Gnao1<tm2.1Rneu>/Gnao1<+>	129S-Gnao1<tm2.1Rneu>	Y	24700286
MGI:5620505	F	MP:0005386	behavior/neurological phenotype	Gnao1<tm2.1Rneu>/Gnao1<+>	(C57BL/6J x 129S1/SvImJ)F1	Y	24700286
MGI:5620768	F	MP:0001926	female infertility	Lhx9<tm1.1(cre/ERT2)Gan>/Lhx9<tm1.1(cre/ERT2)Gan>	involves: 129S6/SvEvTac * C57BL/6J	N	25112520
MGI:5620953	F	MP:0009710	anhedonia	Tg(Camk2a-Magi2)1Shlee/?	C57BL/6J-Tg(Camk2a-Magi2)1Shlee	N	25653350
MGI:5620953	F	MP:0001360	abnormal social investigation	Tg(Camk2a-Magi2)1Shlee/?	C57BL/6J-Tg(Camk2a-Magi2)1Shlee	N	25653350
MGI:5620953	M	MP:0008428	abnormal spatial working memory	Tg(Camk2a-Magi2)1Shlee/?	C57BL/6J-Tg(Camk2a-Magi2)1Shlee	N	25653350
MGI:5620953	F	MP:0001447	abnormal nest building behavior	Tg(Camk2a-Magi2)1Shlee/?	C57BL/6J-Tg(Camk2a-Magi2)1Shlee	N	25653350
MGI:5620953	M	MP:0031391	increased locomotor activity	Tg(Camk2a-Magi2)1Shlee/?	C57BL/6J-Tg(Camk2a-Magi2)1Shlee	N	25653350
MGI:5620953	M	MP:0002557	abnormal social/conspecific interaction behavior	Tg(Camk2a-Magi2)1Shlee/?	C57BL/6J-Tg(Camk2a-Magi2)1Shlee	N	25653350
MGI:5620953	M	MP:0001473	reduced long-term potentiation	Tg(Camk2a-Magi2)1Shlee/?	C57BL/6J-Tg(Camk2a-Magi2)1Shlee	N	25653350
MGI:5620953	F	MP:0004209	abnormal sweet taste sensitivity	Tg(Camk2a-Magi2)1Shlee/?	C57BL/6J-Tg(Camk2a-Magi2)1Shlee	N	25653350
MGI:5620953	M	MP:0001363	increased anxiety-related response	Tg(Camk2a-Magi2)1Shlee/?	C57BL/6J-Tg(Camk2a-Magi2)1Shlee	N	25653350
MGI:5629811	M	MP:0001360	abnormal social investigation	Pten<tm1Engc>/Pten<tm1Engc>	involves: CD-1	N	24470394
MGI:5629811	M	MP:0001265	decreased body size	Pten<tm1Engc>/Pten<tm1Engc>	involves: CD-1	N	24470394
MGI:5629844	M	MP:0005280	abnormal fatty acids level	Hprt1<tm6(CAG-fat-1)Geno>/Y,Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	24622775
MGI:5629845	F	MP:0005280	abnormal fatty acids level	Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<+>,Hprt1<tm6(CAG-fat-1)Geno>/Hprt1<tm6(CAG-fat-1)Geno>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	24622775
MGI:5629953	M	MP:0001932	abnormal spermiogenesis	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	N	24778225
MGI:5629953	M	MP:0001146	abnormal testis morphology	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	N	24778225
MGI:5629953	M	MP:0005578	teratozoospermia	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	N	24778225
MGI:5629953	M	MP:0004777	abnormal phospholipid level	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	N	24778225
MGI:5629953	M	MP:0002687	oligozoospermia	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	N	24778225
MGI:5629953	M	MP:0009230	abnormal sperm head morphology	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	N	24778225
MGI:5629953	M	MP:0008892	abnormal sperm flagellum morphology	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	N	24778225
MGI:5629953	M	MP:0002675	asthenozoospermia	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	N	24778225
MGI:5629953	M	MP:0006362	abnormal male germ cell morphology	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	N	24778225
MGI:5629953	M	MP:0001925	male infertility	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	N	24778225
MGI:5629953	M	MP:0006380	abnormal spermatid morphology	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	N	24778225
MGI:5629953	M	MP:0005376	homeostasis/metabolism phenotype	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	Y	24778225
MGI:5629953	M	MP:0005375	adipose tissue phenotype	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	Y	24778225
MGI:5629953	M	MP:0001156	abnormal spermatogenesis	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * 129S4/SvJaeSor * FVB/N	N	24778225
MGI:5629954	M	MP:0005389	reproductive system phenotype	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Fabp4-cre)1Rev/0	involves: 129 * 129S4/SvJaeSor	Y	24778225
MGI:5629954	M	MP:0011174	lipodystrophy	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Fabp4-cre)1Rev/0	involves: 129 * 129S4/SvJaeSor	N	24778225
MGI:5629954	M	MP:0005178	increased circulating cholesterol level	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Fabp4-cre)1Rev/0	involves: 129 * 129S4/SvJaeSor	N	24778225
MGI:5629954	M	MP:0002079	increased circulating insulin level	Bscl2<tm1.1Gliu>/Bscl2<tm1.1Gliu>,Tg(Fabp4-cre)1Rev/0	involves: 129 * 129S4/SvJaeSor	N	24778225
MGI:5630794	M	MP:0003036	vertebral transformation	1110059G10Rik<tm1a(KOMP)Wtsi>/1110059G10Rik<tm1a(KOMP)Wtsi>	C57BL/6N-1110059G10Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630803	M	MP:0000438	abnormal cranium morphology	4933402N03Rik<tm2a(KOMP)Wtsi>/4933402N03Rik<tm2a(KOMP)Wtsi>	C57BL/6N-4933402N03Rik<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630803	F	MP:0002073	abnormal hair growth	4933402N03Rik<tm2a(KOMP)Wtsi>/4933402N03Rik<tm2a(KOMP)Wtsi>	C57BL/6N-4933402N03Rik<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630803	F	MP:0000194	increased circulating calcium level	4933402N03Rik<tm2a(KOMP)Wtsi>/4933402N03Rik<tm2a(KOMP)Wtsi>	C57BL/6N-4933402N03Rik<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630803	F	MP:0010088	decreased circulating fructosamine level	4933402N03Rik<tm2a(KOMP)Wtsi>/4933402N03Rik<tm2a(KOMP)Wtsi>	C57BL/6N-4933402N03Rik<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630808	M	MP:0000062	increased bone mineral density	A430005L14Rik<tm1a(KOMP)Wtsi>/A430005L14Rik<tm1a(KOMP)Wtsi>	C57BL/6N-A430005L14Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630808	M	MP:0003960	increased lean body mass	A430005L14Rik<tm1a(KOMP)Wtsi>/A430005L14Rik<tm1a(KOMP)Wtsi>	C57BL/6N-A430005L14Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630808	M	MP:0010025	decreased total body fat amount	A430005L14Rik<tm1a(KOMP)Wtsi>/A430005L14Rik<tm1a(KOMP)Wtsi>	C57BL/6N-A430005L14Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630808	M	MP:0010123	increased bone mineral content	A430005L14Rik<tm1a(KOMP)Wtsi>/A430005L14Rik<tm1a(KOMP)Wtsi>	C57BL/6N-A430005L14Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630815	F	MP:0010052	increased grip strength	Abtb2<tm1a(KOMP)Wtsi>/Abtb2<tm1a(KOMP)Wtsi>	C57BL/6N-A<tm1Brd> Abtb2<tm1a(KOMP)Wtsi>/WtsiH	N	MGI:5576271
MGI:5630815	M	MP:0000221	decreased leukocyte cell number	Abtb2<tm1a(KOMP)Wtsi>/Abtb2<tm1a(KOMP)Wtsi>	C57BL/6N-A<tm1Brd> Abtb2<tm1a(KOMP)Wtsi>/WtsiH	N	MGI:5576271
MGI:5630822	M	MP:0005344	increased circulating bilirubin level	Acsl5<tm1.1(KOMP)Vlcg>/Acsl5<tm1.1(KOMP)Vlcg>	C57BL/6N-Acsl5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630822	F	MP:0001314	cornea opacity	Acsl5<tm1.1(KOMP)Vlcg>/Acsl5<tm1.1(KOMP)Vlcg>	C57BL/6N-Acsl5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630822	M	MP:0003402	decreased liver weight	Acsl5<tm1.1(KOMP)Vlcg>/Acsl5<tm1.1(KOMP)Vlcg>	C57BL/6N-Acsl5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630822	M	MP:0002644	decreased circulating triglyceride level	Acsl5<tm1.1(KOMP)Vlcg>/Acsl5<tm1.1(KOMP)Vlcg>	C57BL/6N-Acsl5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630822	F	MP:0002833	increased heart weight	Acsl5<tm1.1(KOMP)Vlcg>/Acsl5<tm1.1(KOMP)Vlcg>	C57BL/6N-Acsl5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630822	M	MP:0000186	decreased circulating HDL cholesterol level	Acsl5<tm1.1(KOMP)Vlcg>/Acsl5<tm1.1(KOMP)Vlcg>	C57BL/6N-Acsl5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630822	F	MP:0001303	abnormal lens morphology	Acsl5<tm1.1(KOMP)Vlcg>/Acsl5<tm1.1(KOMP)Vlcg>	C57BL/6N-Acsl5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630822	M	MP:0005567	decreased circulating total protein level	Acsl5<tm1.1(KOMP)Vlcg>/Acsl5<tm1.1(KOMP)Vlcg>	C57BL/6N-Acsl5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630822	M	MP:0004952	increased spleen weight	Acsl5<tm1.1(KOMP)Vlcg>/Acsl5<tm1.1(KOMP)Vlcg>	C57BL/6N-Acsl5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630828	F	MP:0011100	preweaning lethality, complete penetrance	Acvr2b<tm1.1(KOMP)Vlcg>/Acvr2b<tm1.1(KOMP)Vlcg>	C57BL/6N-Acvr2b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630829	F	MP:0002608	increased hematocrit	Adamts18<tm1.1(KOMP)Vlcg>/Adamts18<tm1.1(KOMP)Vlcg>	C57BL/6N-Adamts18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630829	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Adamts18<tm1.1(KOMP)Vlcg>/Adamts18<tm1.1(KOMP)Vlcg>	C57BL/6N-Adamts18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630829	F	MP:0002590	increased mean corpuscular volume	Adamts18<tm1.1(KOMP)Vlcg>/Adamts18<tm1.1(KOMP)Vlcg>	C57BL/6N-Adamts18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630834	F	MP:0000219	increased neutrophil cell number	Afap1l2<tm1b(KOMP)Wtsi>/Afap1l2<tm1b(KOMP)Wtsi>	C57BL/6N-Afap1l2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630834	M	MP:0010506	prolonged RR interval	Afap1l2<tm1b(KOMP)Wtsi>/Afap1l2<tm1b(KOMP)Wtsi>	C57BL/6N-Afap1l2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630834	F	MP:0002968	increased circulating alkaline phosphatase level	Afap1l2<tm1b(KOMP)Wtsi>/Afap1l2<tm1b(KOMP)Wtsi>	C57BL/6N-Afap1l2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630834	F	MP:0000689	abnormal spleen morphology	Afap1l2<tm1b(KOMP)Wtsi>/Afap1l2<tm1b(KOMP)Wtsi>	C57BL/6N-Afap1l2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630834	M	MP:0005333	decreased heart rate	Afap1l2<tm1b(KOMP)Wtsi>/Afap1l2<tm1b(KOMP)Wtsi>	C57BL/6N-Afap1l2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630834	M	MP:0010025	decreased total body fat amount	Afap1l2<tm1b(KOMP)Wtsi>/Afap1l2<tm1b(KOMP)Wtsi>	C57BL/6N-Afap1l2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630834	M	MP:0000367	abnormal coat/ hair morphology	Afap1l2<tm1b(KOMP)Wtsi>/Afap1l2<tm1b(KOMP)Wtsi>	C57BL/6N-Afap1l2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630834	M	MP:0010123	increased bone mineral content	Afap1l2<tm1b(KOMP)Wtsi>/Afap1l2<tm1b(KOMP)Wtsi>	C57BL/6N-Afap1l2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630836	M	MP:0005559	increased circulating glucose level	Afmid<tm1b(EUCOMM)Wtsi>/Afmid<tm1b(EUCOMM)Wtsi>	C57BL/6N-Afmid<tm1b(EUCOMM)Wtsi>/H	N	26432886
MGI:5630836	M	MP:0005559	increased circulating glucose level	Afmid<tm1b(EUCOMM)Wtsi>/Afmid<tm1b(EUCOMM)Wtsi>	C57BL/6N-Afmid<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5630836	M	MP:0001399	hyperactivity	Afmid<tm1b(EUCOMM)Wtsi>/Afmid<tm1b(EUCOMM)Wtsi>	C57BL/6N-Afmid<tm1b(EUCOMM)Wtsi>/H	N	26432886
MGI:5630836	M	MP:0009168	decreased pancreatic islet number	Afmid<tm1b(EUCOMM)Wtsi>/Afmid<tm1b(EUCOMM)Wtsi>	C57BL/6N-Afmid<tm1b(EUCOMM)Wtsi>/H	N	26432886
MGI:5630836	M	MP:0002590	increased mean corpuscular volume	Afmid<tm1b(EUCOMM)Wtsi>/Afmid<tm1b(EUCOMM)Wtsi>	C57BL/6N-Afmid<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5630836	M	MP:0005215	abnormal pancreatic islet morphology	Afmid<tm1b(EUCOMM)Wtsi>/Afmid<tm1b(EUCOMM)Wtsi>	C57BL/6N-Afmid<tm1b(EUCOMM)Wtsi>/H	N	26432886
MGI:5630836	M	MP:0010087	increased circulating fructosamine level	Afmid<tm1b(EUCOMM)Wtsi>/Afmid<tm1b(EUCOMM)Wtsi>	C57BL/6N-Afmid<tm1b(EUCOMM)Wtsi>/H	N	26432886
MGI:5630837	F	MP:0005627	increased circulating potassium level	Agap1<tm1a(EUCOMM)Wtsi>/Agap1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Agap1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630837	F	MP:0001303	abnormal lens morphology	Agap1<tm1a(EUCOMM)Wtsi>/Agap1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Agap1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630837	M	MP:0001312	abnormal cornea morphology	Agap1<tm1a(EUCOMM)Wtsi>/Agap1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Agap1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630837	M	MP:0001314	cornea opacity	Agap1<tm1a(EUCOMM)Wtsi>/Agap1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Agap1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630837	F	MP:0001304	cataract	Agap1<tm1a(EUCOMM)Wtsi>/Agap1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Agap1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630837	F	MP:0000443	abnormal snout morphology	Agap1<tm1a(EUCOMM)Wtsi>/Agap1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Agap1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630837	M	MP:0001307	fused cornea and lens	Agap1<tm1a(EUCOMM)Wtsi>/Agap1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Agap1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630837	F	MP:0000438	abnormal cranium morphology	Agap1<tm1a(EUCOMM)Wtsi>/Agap1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Agap1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630838	F	MP:0010052	increased grip strength	Ago3<tm1a(KOMP)Wtsi>/Ago3<tm1a(KOMP)Wtsi>	C57BL/6N-Ago3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630848	F	MP:0009806	abnormal otic vesicle morphology	Alg10b<tm1.1(KOMP)Vlcg>/Alg10b<tm1.1(KOMP)Vlcg>	C57BL/6N-Alg10b<tm1.1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5630851	M	MP:0003960	increased lean body mass	Ankrd9<tm1(KOMP)Wtsi>/Ankrd9<tm1(KOMP)Wtsi>	C57BL/6N-Ankrd9<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630851	M	MP:0002875	decreased erythrocyte cell number	Ankrd9<tm1(KOMP)Wtsi>/Ankrd9<tm1(KOMP)Wtsi>	C57BL/6N-Ankrd9<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630851	M	MP:0001257	increased body length	Ankrd9<tm1(KOMP)Wtsi>/Ankrd9<tm1(KOMP)Wtsi>	C57BL/6N-Ankrd9<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630851	M	MP:0010025	decreased total body fat amount	Ankrd9<tm1(KOMP)Wtsi>/Ankrd9<tm1(KOMP)Wtsi>	C57BL/6N-Ankrd9<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630857	M	MP:0005561	increased mean corpuscular hemoglobin	Arhgap22<tm1a(KOMP)Wtsi>/Arhgap22<tm1a(KOMP)Wtsi>	C57BL/6N-Arhgap22<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630857	M	MP:0000183	decreased circulating LDL cholesterol level	Arhgap22<tm1a(KOMP)Wtsi>/Arhgap22<tm1a(KOMP)Wtsi>	C57BL/6N-Arhgap22<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630860	M	MP:0005178	increased circulating cholesterol level	Arhgef38<tm1a(KOMP)Wtsi>/Arhgef38<tm1a(KOMP)Wtsi>	C57BL/6N-Arhgef38<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630864	M	MP:0003961	decreased lean body mass	Arl10<tm1.1(KOMP)Vlcg>/Arl10<tm1.1(KOMP)Vlcg>	C57BL/6N-Arl10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630864	M	MP:0010024	increased total body fat amount	Arl10<tm1.1(KOMP)Vlcg>/Arl10<tm1.1(KOMP)Vlcg>	C57BL/6N-Arl10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630865	F	MP:0010206	pigment incontinence	Arpc1b<tm1a(EUCOMM)Wtsi>/Arpc1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arpc1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	25340873
MGI:5630865	F	MP:0002966	decreased circulating alkaline phosphatase level	Arpc1b<tm1a(EUCOMM)Wtsi>/Arpc1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arpc1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630865	F	MP:0009932	skin fibrosis	Arpc1b<tm1a(EUCOMM)Wtsi>/Arpc1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arpc1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	25340873
MGI:5630865	F	MP:0010088	decreased circulating fructosamine level	Arpc1b<tm1a(EUCOMM)Wtsi>/Arpc1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arpc1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630865	M	MP:0000194	increased circulating calcium level	Arpc1b<tm1a(EUCOMM)Wtsi>/Arpc1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arpc1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630865	F	MP:0005505	thrombocytosis	Arpc1b<tm1a(EUCOMM)Wtsi>/Arpc1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arpc1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630865	F	MP:0000218	increased leukocyte cell number	Arpc1b<tm1a(EUCOMM)Wtsi>/Arpc1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arpc1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630865	F	MP:0010067	increased red blood cell distribution width	Arpc1b<tm1a(EUCOMM)Wtsi>/Arpc1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arpc1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630865	M	MP:0004609	vertebral fusion	Arpc1b<tm1a(EUCOMM)Wtsi>/Arpc1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arpc1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630865	M	MP:0004613	fusion of vertebral arches	Arpc1b<tm1a(EUCOMM)Wtsi>/Arpc1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arpc1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630865	F	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Arpc1b<tm1a(EUCOMM)Wtsi>/Arpc1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arpc1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630865	F	MP:0005562	decreased mean corpuscular hemoglobin	Arpc1b<tm1a(EUCOMM)Wtsi>/Arpc1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arpc1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630865	M	MP:0001258	decreased body length	Arpc1b<tm1a(EUCOMM)Wtsi>/Arpc1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arpc1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630866	M	MP:0002833	increased heart weight	Asb10<tm2b(KOMP)Wtsi>/Asb10<tm2b(KOMP)Wtsi>	B6N(Cg)-Asb10<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630866	M	MP:0005564	increased hemoglobin content	Asb10<tm2b(KOMP)Wtsi>/Asb10<tm2b(KOMP)Wtsi>	B6N(Cg)-Asb10<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630871	M	MP:0002151	abnormal neural tube morphology	Asf1a<tm1b(KOMP)Wtsi>/Asf1a<tm1b(KOMP)Wtsi>	B6N(Cg)-Asf1a<tm1b(KOMP)Wtsi>/2J	N	MGI:5576271
MGI:5630871	M	MP:0003720	abnormal neural tube closure	Asf1a<tm1b(KOMP)Wtsi>/Asf1a<tm1b(KOMP)Wtsi>	B6N(Cg)-Asf1a<tm1b(KOMP)Wtsi>/2J	N	MGI:5576271
MGI:5630885	M	MP:0010123	increased bone mineral content	Atp8b2<tm1a(KOMP)Wtsi>/Atp8b2<tm1a(KOMP)Wtsi>	C57BL/6N-Atp8b2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630885	M	MP:0002968	increased circulating alkaline phosphatase level	Atp8b2<tm1a(KOMP)Wtsi>/Atp8b2<tm1a(KOMP)Wtsi>	C57BL/6N-Atp8b2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630885	M	MP:0005419	decreased circulating serum albumin level	Atp8b2<tm1a(KOMP)Wtsi>/Atp8b2<tm1a(KOMP)Wtsi>	C57BL/6N-Atp8b2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630886	M	MP:0005560	decreased circulating glucose level	Atr<tm1b(KOMP)Wtsi>/Atr<+>	B6N(Cg)-Atr<tm1b(KOMP)Wtsi>/2J	N	MGI:5576271
MGI:5630886	M	MP:0002833	increased heart weight	Atr<tm1b(KOMP)Wtsi>/Atr<+>	B6N(Cg)-Atr<tm1b(KOMP)Wtsi>/2J	N	MGI:5576271
MGI:5630886	F	MP:0000955	abnormal spinal cord morphology	Atr<tm1b(KOMP)Wtsi>/Atr<+>	B6N(Cg)-Atr<tm1b(KOMP)Wtsi>/2J	N	MGI:5576271
MGI:5630906	F	MP:0003179	thrombocytopenia	Bloc1s2<tm1.1(KOMP)Mbp>/Bloc1s2<+>	B6N(Cg)-Bloc1s2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630906	F	MP:0002941	increased circulating alanine transaminase level	Bloc1s2<tm1.1(KOMP)Mbp>/Bloc1s2<+>	B6N(Cg)-Bloc1s2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630906	M	MP:0002702	decreased circulating free fatty acids level	Bloc1s2<tm1.1(KOMP)Mbp>/Bloc1s2<+>	B6N(Cg)-Bloc1s2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630907	M	MP:0000428	abnormal craniofacial morphology	Bloc1s2<tm1.1(KOMP)Mbp>/Bloc1s2<tm1.1(KOMP)Mbp>	B6N(Cg)-Bloc1s2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630907	M	MP:0005650	abnormal limb bud morphology	Bloc1s2<tm1.1(KOMP)Mbp>/Bloc1s2<tm1.1(KOMP)Mbp>	B6N(Cg)-Bloc1s2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630907	M	MP:0000288	abnormal pericardium morphology	Bloc1s2<tm1.1(KOMP)Mbp>/Bloc1s2<tm1.1(KOMP)Mbp>	B6N(Cg)-Bloc1s2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630907	M	MP:0000603	pale liver	Bloc1s2<tm1.1(KOMP)Mbp>/Bloc1s2<tm1.1(KOMP)Mbp>	B6N(Cg)-Bloc1s2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630912	F	MP:0001488	increased startle reflex	Brms1<tm1.1(KOMP)Vlcg>/Brms1<+>	B6N(Cg)-Brms1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630912	M	MP:0003019	increased circulating chloride level	Brms1<tm1.1(KOMP)Vlcg>/Brms1<+>	B6N(Cg)-Brms1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630914	M	MP:0005561	increased mean corpuscular hemoglobin	Btg2<tm1b(KOMP)Mbp>/Btg2<tm1b(KOMP)Mbp>	B6N(Cg)-Btg2<tm1b(KOMP)Mbp>/2J	N	MGI:5576271
MGI:5630914	M	MP:0001399	hyperactivity	Btg2<tm1b(KOMP)Mbp>/Btg2<tm1b(KOMP)Mbp>	B6N(Cg)-Btg2<tm1b(KOMP)Mbp>/2J	N	MGI:5576271
MGI:5630914	F	MP:0004906	enlarged uterus	Btg2<tm1b(KOMP)Mbp>/Btg2<tm1b(KOMP)Mbp>	B6N(Cg)-Btg2<tm1b(KOMP)Mbp>/2J	N	MGI:5576271
MGI:5630914	M	MP:0002590	increased mean corpuscular volume	Btg2<tm1b(KOMP)Mbp>/Btg2<tm1b(KOMP)Mbp>	B6N(Cg)-Btg2<tm1b(KOMP)Mbp>/2J	N	MGI:5576271
MGI:5630915	M	MP:0003960	increased lean body mass	Bzw2<tm1b(KOMP)Mbp>/Bzw2<tm1b(KOMP)Mbp>	B6N(Cg)-Bzw2<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630915	M	MP:0004151	decreased circulating iron level	Bzw2<tm1b(KOMP)Mbp>/Bzw2<tm1b(KOMP)Mbp>	B6N(Cg)-Bzw2<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630915	M	MP:0005560	decreased circulating glucose level	Bzw2<tm1b(KOMP)Mbp>/Bzw2<tm1b(KOMP)Mbp>	B6N(Cg)-Bzw2<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630915	M	MP:0005179	decreased circulating cholesterol level	Bzw2<tm1b(KOMP)Mbp>/Bzw2<tm1b(KOMP)Mbp>	B6N(Cg)-Bzw2<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630918	F	MP:0001325	abnormal retina morphology	C1qtnf5<tm1.1(KOMP)Vlcg>/C1qtnf5<+>	B6N(Cg)-C1qtnf5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630920	M	MP:0002833	increased heart weight	C9<tm1.1(KOMP)Vlcg>/C9<tm1.1(KOMP)Vlcg>	B6N(Cg)-C9<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630920	M	MP:0005633	increased circulating sodium level	C9<tm1.1(KOMP)Vlcg>/C9<tm1.1(KOMP)Vlcg>	B6N(Cg)-C9<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630923	F	MP:0005633	increased circulating sodium level	Cacna2d3<tm1b(KOMP)Wtsi>/Cacna2d3<+>	B6N(Cg)-Cacna2d3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630923	F	MP:0002644	decreased circulating triglyceride level	Cacna2d3<tm1b(KOMP)Wtsi>/Cacna2d3<+>	B6N(Cg)-Cacna2d3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630926	F	MP:0005633	increased circulating sodium level	Car7<tm1b(KOMP)Wtsi>/Car7<+>	B6N(Cg)-Car7<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630926	M	MP:0002833	increased heart weight	Car7<tm1b(KOMP)Wtsi>/Car7<+>	B6N(Cg)-Car7<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630927	M	MP:0011100	preweaning lethality, complete penetrance	Casc3<tm1.1(KOMP)Vlcg>/Casc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Casc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630928	M	MP:0003917	increased kidney weight	Caskin2<tm1.1(KOMP)Vlcg>/Caskin2<tm1.1(KOMP)Vlcg>	C57BL/6N-Caskin2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630928	M	MP:0009142	decreased prepulse inhibition	Caskin2<tm1.1(KOMP)Vlcg>/Caskin2<tm1.1(KOMP)Vlcg>	C57BL/6N-Caskin2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630928	M	MP:0000062	increased bone mineral density	Caskin2<tm1.1(KOMP)Vlcg>/Caskin2<tm1.1(KOMP)Vlcg>	C57BL/6N-Caskin2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630929	F	MP:0005344	increased circulating bilirubin level	Casp4<tm1b(KOMP)Wtsi>/Casp4<tm1b(KOMP)Wtsi>	C57BL/6N-Casp4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630929	F	MP:0000194	increased circulating calcium level	Casp4<tm1b(KOMP)Wtsi>/Casp4<tm1b(KOMP)Wtsi>	C57BL/6N-Casp4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630929	F	MP:0005559	increased circulating glucose level	Casp4<tm1b(KOMP)Wtsi>/Casp4<tm1b(KOMP)Wtsi>	C57BL/6N-Casp4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630929	M	MP:0002079	increased circulating insulin level	Casp4<tm1b(KOMP)Wtsi>/Casp4<tm1b(KOMP)Wtsi>	C57BL/6N-Casp4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630931	M	MP:0001489	decreased startle reflex	Cast<tm1.1(KOMP)Vlcg>/Cast<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cast<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:5630931	F	MP:0012000	abnormal limb position	Cast<tm1.1(KOMP)Vlcg>/Cast<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cast<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:5630931	F	MP:0000579	abnormal nail morphology	Cast<tm1.1(KOMP)Vlcg>/Cast<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cast<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:5630931	F	MP:0001406	abnormal gait	Cast<tm1.1(KOMP)Vlcg>/Cast<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cast<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:5630931	M	MP:0001566	increased circulating phosphate level	Cast<tm1.1(KOMP)Vlcg>/Cast<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cast<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:5630931	M	MP:0002941	increased circulating alanine transaminase level	Cast<tm1.1(KOMP)Vlcg>/Cast<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cast<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:5630931	F	MP:0002110	abnormal digit morphology	Cast<tm1.1(KOMP)Vlcg>/Cast<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cast<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:5630931	F	MP:0002833	increased heart weight	Cast<tm1.1(KOMP)Vlcg>/Cast<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cast<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:5630932	F	MP:0011396	abnormal sleep behavior	Cbln3<tm1.1(KOMP)Vlcg>/Cbln3<+>	B6N(Cg)-Cbln3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630938	M	MP:0003960	increased lean body mass	Ccdc122<tm1a(KOMP)Wtsi>/Ccdc122<tm1a(KOMP)Wtsi>	C57BL/6N-Ccdc122<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630938	M	MP:0011939	increased food intake	Ccdc122<tm1a(KOMP)Wtsi>/Ccdc122<tm1a(KOMP)Wtsi>	C57BL/6N-Ccdc122<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630938	M	MP:0010378	increased respiratory quotient	Ccdc122<tm1a(KOMP)Wtsi>/Ccdc122<tm1a(KOMP)Wtsi>	C57BL/6N-Ccdc122<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630938	M	MP:0010025	decreased total body fat amount	Ccdc122<tm1a(KOMP)Wtsi>/Ccdc122<tm1a(KOMP)Wtsi>	C57BL/6N-Ccdc122<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630938	M	MP:0010067	increased red blood cell distribution width	Ccdc122<tm1a(KOMP)Wtsi>/Ccdc122<tm1a(KOMP)Wtsi>	C57BL/6N-Ccdc122<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630941	M	MP:0001925	male infertility	Ccdc159<tm1a(KOMP)Wtsi>/Ccdc159<tm1a(KOMP)Wtsi>	C57BL/6N-Ccdc159<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630945	M	MP:0010123	increased bone mineral content	Cd300lg<tm1a(KOMP)Wtsi>/Cd300lg<tm1a(KOMP)Wtsi>	C57BL/6N-Cd300lg<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630945	F	MP:0004509	abnormal pelvic girdle bone morphology	Cd300lg<tm1a(KOMP)Wtsi>/Cd300lg<tm1a(KOMP)Wtsi>	C57BL/6N-Cd300lg<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630945	M	MP:0011939	increased food intake	Cd300lg<tm1a(KOMP)Wtsi>/Cd300lg<tm1a(KOMP)Wtsi>	C57BL/6N-Cd300lg<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630945	M	MP:0003960	increased lean body mass	Cd300lg<tm1a(KOMP)Wtsi>/Cd300lg<tm1a(KOMP)Wtsi>	C57BL/6N-Cd300lg<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630945	M	MP:0010025	decreased total body fat amount	Cd300lg<tm1a(KOMP)Wtsi>/Cd300lg<tm1a(KOMP)Wtsi>	C57BL/6N-Cd300lg<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5630946	M	MP:0013279	increased fasting circulating glucose level	Cdc20<tm1.1(KOMP)Vlcg>/Cdc20<+>	B6N(Cg)-Cdc20<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630946	M	MP:0005292	improved glucose tolerance	Cdc20<tm1.1(KOMP)Vlcg>/Cdc20<+>	B6N(Cg)-Cdc20<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630946	F	MP:0005559	increased circulating glucose level	Cdc20<tm1.1(KOMP)Vlcg>/Cdc20<+>	B6N(Cg)-Cdc20<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630946	F	MP:0010052	increased grip strength	Cdc20<tm1.1(KOMP)Vlcg>/Cdc20<+>	B6N(Cg)-Cdc20<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630946	M	MP:0002833	increased heart weight	Cdc20<tm1.1(KOMP)Vlcg>/Cdc20<+>	B6N(Cg)-Cdc20<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630946	M	MP:0005560	decreased circulating glucose level	Cdc20<tm1.1(KOMP)Vlcg>/Cdc20<+>	B6N(Cg)-Cdc20<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630955	M	MP:0002702	decreased circulating free fatty acids level	Ceacam16<tm1.1(KOMP)Wtsi>/Ceacam16<tm1.1(KOMP)Wtsi>	B6N(Cg)-Ceacam16<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630955	M	MP:0005633	increased circulating sodium level	Ceacam16<tm1.1(KOMP)Wtsi>/Ceacam16<tm1.1(KOMP)Wtsi>	B6N(Cg)-Ceacam16<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630955	M	MP:0012121	sclerocornea	Ceacam16<tm1.1(KOMP)Wtsi>/Ceacam16<tm1.1(KOMP)Wtsi>	B6N(Cg)-Ceacam16<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630959	F	MP:0004151	decreased circulating iron level	Cenpo<tm1b(KOMP)Mbp>/Cenpo<+>	B6N(Cg)-Cenpo<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630959	M	MP:0005179	decreased circulating cholesterol level	Cenpo<tm1b(KOMP)Mbp>/Cenpo<+>	B6N(Cg)-Cenpo<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630959	M	MP:0002833	increased heart weight	Cenpo<tm1b(KOMP)Mbp>/Cenpo<+>	B6N(Cg)-Cenpo<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630959	M	MP:0005560	decreased circulating glucose level	Cenpo<tm1b(KOMP)Mbp>/Cenpo<+>	B6N(Cg)-Cenpo<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630959	M	MP:0000186	decreased circulating HDL cholesterol level	Cenpo<tm1b(KOMP)Mbp>/Cenpo<+>	B6N(Cg)-Cenpo<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630959	F	MP:0000195	decreased circulating calcium level	Cenpo<tm1b(KOMP)Mbp>/Cenpo<+>	B6N(Cg)-Cenpo<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630959	M	MP:0002644	decreased circulating triglyceride level	Cenpo<tm1b(KOMP)Mbp>/Cenpo<+>	B6N(Cg)-Cenpo<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630959	F	MP:0005566	decreased blood urea nitrogen level	Cenpo<tm1b(KOMP)Mbp>/Cenpo<+>	B6N(Cg)-Cenpo<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630961	F	MP:0000063	decreased bone mineral density	Cers5<tm2b(KOMP)Mbp>/Cers5<tm2b(KOMP)Mbp>	B6N(Cg)-Cers5<tm2b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630961	F	MP:0001417	decreased exploration in new environment	Cers5<tm2b(KOMP)Mbp>/Cers5<tm2b(KOMP)Mbp>	B6N(Cg)-Cers5<tm2b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630961	F	MP:0010124	decreased bone mineral content	Cers5<tm2b(KOMP)Mbp>/Cers5<tm2b(KOMP)Mbp>	B6N(Cg)-Cers5<tm2b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630961	F	MP:0020870	decreased thigmotaxis	Cers5<tm2b(KOMP)Mbp>/Cers5<tm2b(KOMP)Mbp>	B6N(Cg)-Cers5<tm2b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630961	M	MP:0005633	increased circulating sodium level	Cers5<tm2b(KOMP)Mbp>/Cers5<tm2b(KOMP)Mbp>	B6N(Cg)-Cers5<tm2b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630961	F	MP:0003795	abnormal bone structure	Cers5<tm2b(KOMP)Mbp>/Cers5<tm2b(KOMP)Mbp>	B6N(Cg)-Cers5<tm2b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630961	F	MP:0001516	abnormal motor coordination/balance	Cers5<tm2b(KOMP)Mbp>/Cers5<tm2b(KOMP)Mbp>	B6N(Cg)-Cers5<tm2b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630962	M	MP:0001925	male infertility	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	C57BL/6N-Cfap69<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630962	M	MP:0011110	preweaning lethality, incomplete penetrance	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	C57BL/6N-Cfap69<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5630963	F	MP:0001575	cyanosis	Cgn<tm1b(KOMP)Wtsi>/Cgn<tm1b(KOMP)Wtsi>	B6N(Cg)-Cgn<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630963	F	MP:0000783	abnormal forebrain morphology	Cgn<tm1b(KOMP)Wtsi>/Cgn<tm1b(KOMP)Wtsi>	B6N(Cg)-Cgn<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630963	F	MP:0003720	abnormal neural tube closure	Cgn<tm1b(KOMP)Wtsi>/Cgn<tm1b(KOMP)Wtsi>	B6N(Cg)-Cgn<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630963	F	MP:0002111	abnormal tail morphology	Cgn<tm1b(KOMP)Wtsi>/Cgn<tm1b(KOMP)Wtsi>	B6N(Cg)-Cgn<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630965	M	MP:0005560	decreased circulating glucose level	Chn1<tm1.1(KOMP)Vlcg>/Chn1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Chn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630965	F	MP:0002968	increased circulating alkaline phosphatase level	Chn1<tm1.1(KOMP)Vlcg>/Chn1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Chn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630965	F	MP:0010053	decreased grip strength	Chn1<tm1.1(KOMP)Vlcg>/Chn1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Chn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630965	M	MP:0005561	increased mean corpuscular hemoglobin	Chn1<tm1.1(KOMP)Vlcg>/Chn1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Chn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630965	F	MP:0005633	increased circulating sodium level	Chn1<tm1.1(KOMP)Vlcg>/Chn1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Chn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630965	M	MP:0002590	increased mean corpuscular volume	Chn1<tm1.1(KOMP)Vlcg>/Chn1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Chn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630965	M	MP:0010025	decreased total body fat amount	Chn1<tm1.1(KOMP)Vlcg>/Chn1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Chn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630965	M	MP:0003960	increased lean body mass	Chn1<tm1.1(KOMP)Vlcg>/Chn1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Chn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630965	M	MP:0003020	decreased circulating chloride level	Chn1<tm1.1(KOMP)Vlcg>/Chn1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Chn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630965	M	MP:0002608	increased hematocrit	Chn1<tm1.1(KOMP)Vlcg>/Chn1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Chn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630968	F	MP:0001399	hyperactivity	Chtf18<tm1b(KOMP)Wtsi>/Chtf18<+>	B6N(Cg)-Chtf18<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630968	F	MP:0005344	increased circulating bilirubin level	Chtf18<tm1b(KOMP)Wtsi>/Chtf18<+>	B6N(Cg)-Chtf18<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630968	F	MP:0002833	increased heart weight	Chtf18<tm1b(KOMP)Wtsi>/Chtf18<+>	B6N(Cg)-Chtf18<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630972	M	MP:0005633	increased circulating sodium level	Cldn13<tm1.1(KOMP)Vlcg>/Cldn13<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cldn13<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630972	F	MP:0002591	decreased mean corpuscular volume	Cldn13<tm1.1(KOMP)Vlcg>/Cldn13<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cldn13<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630972	F	MP:0005627	increased circulating potassium level	Cldn13<tm1.1(KOMP)Vlcg>/Cldn13<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cldn13<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630972	M	MP:0013278	decreased fasting circulating glucose level	Cldn13<tm1.1(KOMP)Vlcg>/Cldn13<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cldn13<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630973	F	MP:0011396	abnormal sleep behavior	Cldn19<tm1.1(KOMP)Vlcg>/Cldn19<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cldn19<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630973	F	MP:0002833	increased heart weight	Cldn19<tm1.1(KOMP)Vlcg>/Cldn19<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cldn19<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630973	M	MP:0005633	increased circulating sodium level	Cldn19<tm1.1(KOMP)Vlcg>/Cldn19<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cldn19<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630973	M	MP:0002702	decreased circulating free fatty acids level	Cldn19<tm1.1(KOMP)Vlcg>/Cldn19<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cldn19<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630980	M	MP:0011100	preweaning lethality, complete penetrance	Cnr1<tm1.1(KOMP)Vlcg>/Cnr1<tm1.1(KOMP)Vlcg>	C57BL/6N-Cnr1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5630984	M	MP:0005560	decreased circulating glucose level	Col18a1<tm1.1(KOMP)Vlcg>/Col18a1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Col18a1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630984	M	MP:0001303	abnormal lens morphology	Col18a1<tm1.1(KOMP)Vlcg>/Col18a1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Col18a1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630984	M	MP:0000186	decreased circulating HDL cholesterol level	Col18a1<tm1.1(KOMP)Vlcg>/Col18a1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Col18a1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630984	F	MP:0001554	increased circulating free fatty acids level	Col18a1<tm1.1(KOMP)Vlcg>/Col18a1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Col18a1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630984	F	MP:0002574	increased vertical activity	Col18a1<tm1.1(KOMP)Vlcg>/Col18a1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Col18a1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630984	F	MP:0001552	increased circulating triglyceride level	Col18a1<tm1.1(KOMP)Vlcg>/Col18a1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Col18a1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630984	F	MP:0013279	increased fasting circulating glucose level	Col18a1<tm1.1(KOMP)Vlcg>/Col18a1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Col18a1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630984	F	MP:0001325	abnormal retina morphology	Col18a1<tm1.1(KOMP)Vlcg>/Col18a1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Col18a1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630984	F	MP:0006241	abnormal placement of pupils	Col18a1<tm1.1(KOMP)Vlcg>/Col18a1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Col18a1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5630988	M	MP:0001289	persistence of hyaloid vascular system	Coq6<tm1b(EUCOMM)Hmgu>/Coq6<+>	C57BL/6N-Coq6<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5630988	M	MP:0013279	increased fasting circulating glucose level	Coq6<tm1b(EUCOMM)Hmgu>/Coq6<+>	C57BL/6N-Coq6<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5630988	F	MP:0002699	abnormal vitreous body morphology	Coq6<tm1b(EUCOMM)Hmgu>/Coq6<+>	C57BL/6N-Coq6<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5630994	F	MP:0013279	increased fasting circulating glucose level	Cox7c<tm1b(KOMP)Mbp>/Cox7c<+>	B6N(Cg)-Cox7c<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5630996	M	MP:0002874	decreased hemoglobin content	Cp<tm1b(KOMP)Wtsi>/Cp<tm1b(KOMP)Wtsi>	B6N(Cg)-Cp<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630996	M	MP:0002833	increased heart weight	Cp<tm1b(KOMP)Wtsi>/Cp<tm1b(KOMP)Wtsi>	B6N(Cg)-Cp<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630996	F	MP:0011396	abnormal sleep behavior	Cp<tm1b(KOMP)Wtsi>/Cp<tm1b(KOMP)Wtsi>	B6N(Cg)-Cp<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630996	M	MP:0002591	decreased mean corpuscular volume	Cp<tm1b(KOMP)Wtsi>/Cp<tm1b(KOMP)Wtsi>	B6N(Cg)-Cp<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630996	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Cp<tm1b(KOMP)Wtsi>/Cp<tm1b(KOMP)Wtsi>	B6N(Cg)-Cp<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5630996	M	MP:0002067	abnormal sensory capabilities/reflexes/nociception	Cp<tm1b(KOMP)Wtsi>/Cp<tm1b(KOMP)Wtsi>	B6N(Cg)-Cp<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631007	M	MP:0001697	abnormal embryo size	Crispld2<tm1.1(KOMP)Vlcg>/Crispld2<tm1.1(KOMP)Vlcg>	C57BL/6N-Crispld2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631007	M	MP:0000266	abnormal heart morphology	Crispld2<tm1.1(KOMP)Vlcg>/Crispld2<tm1.1(KOMP)Vlcg>	C57BL/6N-Crispld2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631018	M	MP:0001925	male infertility	Cwc27<tm1b(KOMP)Wtsi>/Cwc27<tm1b(KOMP)Wtsi>	B6N(Cg)-Cwc27<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631019	M	MP:0010025	decreased total body fat amount	Cyb5d1<tm1.1(KOMP)Vlcg>/Cyb5d1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cyb5d1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631019	M	MP:0002100	abnormal tooth morphology	Cyb5d1<tm1.1(KOMP)Vlcg>/Cyb5d1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cyb5d1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631019	F	MP:0001486	abnormal startle reflex	Cyb5d1<tm1.1(KOMP)Vlcg>/Cyb5d1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cyb5d1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631019	F	MP:0002702	decreased circulating free fatty acids level	Cyb5d1<tm1.1(KOMP)Vlcg>/Cyb5d1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cyb5d1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631019	F	MP:0001399	hyperactivity	Cyb5d1<tm1.1(KOMP)Vlcg>/Cyb5d1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cyb5d1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631019	F	MP:0005633	increased circulating sodium level	Cyb5d1<tm1.1(KOMP)Vlcg>/Cyb5d1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cyb5d1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631019	M	MP:0000218	increased leukocyte cell number	Cyb5d1<tm1.1(KOMP)Vlcg>/Cyb5d1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cyb5d1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631021	M	MP:0001303	abnormal lens morphology	Cyba<tm1a(EUCOMM)Wtsi>/Cyba<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cyba<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631021	F	MP:0001289	persistence of hyaloid vascular system	Cyba<tm1a(EUCOMM)Wtsi>/Cyba<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cyba<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631021	M	MP:0008805	decreased circulating amylase level	Cyba<tm1a(EUCOMM)Wtsi>/Cyba<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cyba<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631021	M	MP:0003960	increased lean body mass	Cyba<tm1a(EUCOMM)Wtsi>/Cyba<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cyba<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631021	M	MP:0001304	cataract	Cyba<tm1a(EUCOMM)Wtsi>/Cyba<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cyba<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631021	M	MP:0002599	increased mean platelet volume	Cyba<tm1a(EUCOMM)Wtsi>/Cyba<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cyba<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631031	M	MP:0010088	decreased circulating fructosamine level	Dbn1<tm1a(KOMP)Wtsi>/Dbn1<tm1a(KOMP)Wtsi>	C57BL/6N-Dbn1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5631034	M	MP:0005561	increased mean corpuscular hemoglobin	Dcaf10<tm1.1(KOMP)Vlcg>/Dcaf10<tm1.1(KOMP)Vlcg>	C57BL/6N-Dcaf10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631034	M	MP:0002590	increased mean corpuscular volume	Dcaf10<tm1.1(KOMP)Vlcg>/Dcaf10<tm1.1(KOMP)Vlcg>	C57BL/6N-Dcaf10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631034	F	MP:0001399	hyperactivity	Dcaf10<tm1.1(KOMP)Vlcg>/Dcaf10<tm1.1(KOMP)Vlcg>	C57BL/6N-Dcaf10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631035	F	MP:0000137	abnormal vertebrae morphology	Dcdc2c<tm1a(KOMP)Wtsi>/Dcdc2c<tm1a(KOMP)Wtsi>	C57BL/6N-Dcdc2c<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631035	M	MP:0002833	increased heart weight	Dcdc2c<tm1a(KOMP)Wtsi>/Dcdc2c<tm1a(KOMP)Wtsi>	C57BL/6N-Dcdc2c<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631037	M	MP:0005344	increased circulating bilirubin level	Dct<tm1b(KOMP)Mbp>/Dct<tm1b(KOMP)Mbp>	C57BL/6N-Dct<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5631037	F	MP:0001566	increased circulating phosphate level	Dct<tm1b(KOMP)Mbp>/Dct<tm1b(KOMP)Mbp>	C57BL/6N-Dct<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5631046	M	MP:0005560	decreased circulating glucose level	Dhx30<tm1.1(KOMP)Vlcg>/Dhx30<+>	C57BL/6N-Dhx30<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631046	M	MP:0005633	increased circulating sodium level	Dhx30<tm1.1(KOMP)Vlcg>/Dhx30<+>	C57BL/6N-Dhx30<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631046	M	MP:0013279	increased fasting circulating glucose level	Dhx30<tm1.1(KOMP)Vlcg>/Dhx30<+>	C57BL/6N-Dhx30<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631053	M	MP:0004924	abnormal behavior	Dnajb3<tm1.1(KOMP)Vlcg>/Dnajb3<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajb3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631053	M	MP:0001417	decreased exploration in new environment	Dnajb3<tm1.1(KOMP)Vlcg>/Dnajb3<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajb3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631053	M	MP:0020870	decreased thigmotaxis	Dnajb3<tm1.1(KOMP)Vlcg>/Dnajb3<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajb3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631054	F	MP:0013279	increased fasting circulating glucose level	Dnajb7<tm1.1(KOMP)Vlcg>/Dnajb7<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajb7<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631054	F	MP:0002060	abnormal skin morphology	Dnajb7<tm1.1(KOMP)Vlcg>/Dnajb7<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajb7<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631055	M	MP:0003960	increased lean body mass	Dnajc14<tm1.1(KOMP)Vlcg>/Dnajc14<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajc14<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631055	M	MP:0005633	increased circulating sodium level	Dnajc14<tm1.1(KOMP)Vlcg>/Dnajc14<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajc14<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631055	M	MP:0005419	decreased circulating serum albumin level	Dnajc14<tm1.1(KOMP)Vlcg>/Dnajc14<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajc14<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631056	F	MP:0005650	abnormal limb bud morphology	Dnajc16<tm1.1(KOMP)Vlcg>/Dnajc16<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajc16<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631059	M	MP:0002574	increased vertical activity	Dnajc28<tm1.1(KOMP)Vlcg>/Dnajc28<+>	C57BL/6N-Dnajc28<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631061	M	MP:0001554	increased circulating free fatty acids level	Dnajc9<tm1.1(KOMP)Vlcg>/Dnajc9<+>	C57BL/6N-Dnajc9<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631065	F	MP:0010124	decreased bone mineral content	Dnase1l2<tm1(KOMP)Wtsi>/Dnase1l2<tm1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631065	M	MP:0002833	increased heart weight	Dnase1l2<tm1(KOMP)Wtsi>/Dnase1l2<tm1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631065	F	MP:0010024	increased total body fat amount	Dnase1l2<tm1(KOMP)Wtsi>/Dnase1l2<tm1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631065	F	MP:0003795	abnormal bone structure	Dnase1l2<tm1(KOMP)Wtsi>/Dnase1l2<tm1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631067	M	MP:0010052	increased grip strength	Dnmt3a<tm1a(KOMP)Wtsi>/Dnmt3a<tm1a(KOMP)Wtsi>	C57BL/6N-Dnmt3a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631068	M	MP:0000186	decreased circulating HDL cholesterol level	Dnmt3a<tm1b(KOMP)Wtsi>/Dnmt3a<+>	C57BL/6N-Dnmt3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631068	M	MP:0001417	decreased exploration in new environment	Dnmt3a<tm1b(KOMP)Wtsi>/Dnmt3a<+>	C57BL/6N-Dnmt3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631068	F	MP:0010024	increased total body fat amount	Dnmt3a<tm1b(KOMP)Wtsi>/Dnmt3a<+>	C57BL/6N-Dnmt3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631068	M	MP:0005560	decreased circulating glucose level	Dnmt3a<tm1b(KOMP)Wtsi>/Dnmt3a<+>	C57BL/6N-Dnmt3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631068	F	MP:0003961	decreased lean body mass	Dnmt3a<tm1b(KOMP)Wtsi>/Dnmt3a<+>	C57BL/6N-Dnmt3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631068	M	MP:0005179	decreased circulating cholesterol level	Dnmt3a<tm1b(KOMP)Wtsi>/Dnmt3a<+>	C57BL/6N-Dnmt3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631068	F	MP:0003795	abnormal bone structure	Dnmt3a<tm1b(KOMP)Wtsi>/Dnmt3a<+>	C57BL/6N-Dnmt3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631068	F	MP:0000947	convulsive seizures	Dnmt3a<tm1b(KOMP)Wtsi>/Dnmt3a<+>	C57BL/6N-Dnmt3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631069	F	MP:0001697	abnormal embryo size	Dnmt3a<tm1b(KOMP)Wtsi>/Dnmt3a<tm1b(KOMP)Wtsi>	C57BL/6N-Dnmt3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631089	M	MP:0001529	abnormal vocalization	Elfn2<tm1.1(KOMP)Vlcg>/Elfn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Elfn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631089	M	MP:0002574	increased vertical activity	Elfn2<tm1.1(KOMP)Vlcg>/Elfn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Elfn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631089	M	MP:0002135	abnormal kidney morphology	Elfn2<tm1.1(KOMP)Vlcg>/Elfn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Elfn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631089	M	MP:0005011	increased eosinophil cell number	Elfn2<tm1.1(KOMP)Vlcg>/Elfn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Elfn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631090	M	MP:0001304	cataract	Ell2<tm1a(EUCOMM)Wtsi>/Ell2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ell2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631090	F	MP:0010052	increased grip strength	Ell2<tm1a(EUCOMM)Wtsi>/Ell2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ell2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631090	F	MP:0002968	increased circulating alkaline phosphatase level	Ell2<tm1a(EUCOMM)Wtsi>/Ell2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ell2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631090	M	MP:0001303	abnormal lens morphology	Ell2<tm1a(EUCOMM)Wtsi>/Ell2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ell2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631090	M	MP:0005419	decreased circulating serum albumin level	Ell2<tm1a(EUCOMM)Wtsi>/Ell2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ell2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631093	M	MP:0002075	abnormal coat/hair pigmentation	Endog<tm1.1(KOMP)Vlcg>/Endog<tm1.1(KOMP)Vlcg>	C57BL/6N-Endog<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631093	M	MP:0001147	small testis	Endog<tm1.1(KOMP)Vlcg>/Endog<tm1.1(KOMP)Vlcg>	C57BL/6N-Endog<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631093	M	MP:0001146	abnormal testis morphology	Endog<tm1.1(KOMP)Vlcg>/Endog<tm1.1(KOMP)Vlcg>	C57BL/6N-Endog<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631096	M	MP:0010025	decreased total body fat amount	Entpd6<tm1a(KOMP)Wtsi>/Entpd6<tm1a(KOMP)Wtsi>	C57BL/6N-Entpd6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631096	F	MP:0010124	decreased bone mineral content	Entpd6<tm1a(KOMP)Wtsi>/Entpd6<tm1a(KOMP)Wtsi>	C57BL/6N-Entpd6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631096	M	MP:0010067	increased red blood cell distribution width	Entpd6<tm1a(KOMP)Wtsi>/Entpd6<tm1a(KOMP)Wtsi>	C57BL/6N-Entpd6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631096	F	MP:0002111	abnormal tail morphology	Entpd6<tm1a(KOMP)Wtsi>/Entpd6<tm1a(KOMP)Wtsi>	C57BL/6N-Entpd6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631096	F	MP:0002941	increased circulating alanine transaminase level	Entpd6<tm1a(KOMP)Wtsi>/Entpd6<tm1a(KOMP)Wtsi>	C57BL/6N-Entpd6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631099	F	MP:0002135	abnormal kidney morphology	Epb41l4a<tm1b(KOMP)Mbp>/Epb41l4a<tm1b(KOMP)Mbp>	C57BL/6N-Epb41l4a<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631101	M	MP:0011954	shortened PQ interval	Ermp1<tm1.1(KOMP)Vlcg>/Ermp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ermp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631101	M	MP:0003019	increased circulating chloride level	Ermp1<tm1.1(KOMP)Vlcg>/Ermp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ermp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631101	M	MP:0000195	decreased circulating calcium level	Ermp1<tm1.1(KOMP)Vlcg>/Ermp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ermp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631101	F	MP:0005633	increased circulating sodium level	Ermp1<tm1.1(KOMP)Vlcg>/Ermp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ermp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631106	F	MP:0000438	abnormal cranium morphology	Exoc3l2<tm1a(KOMP)Wtsi>/Exoc3l2<tm1a(KOMP)Wtsi>	C57BL/6N-Exoc3l2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631106	F	MP:0000443	abnormal snout morphology	Exoc3l2<tm1a(KOMP)Wtsi>/Exoc3l2<tm1a(KOMP)Wtsi>	C57BL/6N-Exoc3l2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631106	F	MP:0002100	abnormal tooth morphology	Exoc3l2<tm1a(KOMP)Wtsi>/Exoc3l2<tm1a(KOMP)Wtsi>	C57BL/6N-Exoc3l2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631115	F	MP:0002135	abnormal kidney morphology	Fam20a<tm1b(KOMP)Wtsi>/Fam20a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam20a<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631115	F	MP:0001258	decreased body length	Fam20a<tm1b(KOMP)Wtsi>/Fam20a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam20a<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631115	F	MP:0002100	abnormal tooth morphology	Fam20a<tm1b(KOMP)Wtsi>/Fam20a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam20a<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631115	F	MP:0010025	decreased total body fat amount	Fam20a<tm1b(KOMP)Wtsi>/Fam20a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam20a<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631115	F	MP:0010123	increased bone mineral content	Fam20a<tm1b(KOMP)Wtsi>/Fam20a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam20a<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631121	M	MP:0013279	increased fasting circulating glucose level	Far2<tm2b(KOMP)Wtsi>/Far2<tm2b(KOMP)Wtsi>	C57BL/6N-Far2<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631121	F	MP:0002833	increased heart weight	Far2<tm2b(KOMP)Wtsi>/Far2<tm2b(KOMP)Wtsi>	C57BL/6N-Far2<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631126	M	MP:0006203	eye hemorrhage	Fbxo41<tm1.1(KOMP)Vlcg>/Fbxo41<tm1.1(KOMP)Vlcg>	C57BL/6N-Fbxo41<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631126	M	MP:0003917	increased kidney weight	Fbxo41<tm1.1(KOMP)Vlcg>/Fbxo41<tm1.1(KOMP)Vlcg>	C57BL/6N-Fbxo41<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631126	M	MP:0002833	increased heart weight	Fbxo41<tm1.1(KOMP)Vlcg>/Fbxo41<tm1.1(KOMP)Vlcg>	C57BL/6N-Fbxo41<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631127	M	MP:0001925	male infertility	Fbxo47<tm1a(EUCOMM)Wtsi>/Fbxo47<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbxo47<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631128	M	MP:0005561	increased mean corpuscular hemoglobin	Fbxo7<tm1a(EUCOMM)Wtsi>/Fbxo7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbxo7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631128	M	MP:0001925	male infertility	Fbxo7<tm1a(EUCOMM)Wtsi>/Fbxo7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbxo7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631128	F	MP:0000221	decreased leukocyte cell number	Fbxo7<tm1a(EUCOMM)Wtsi>/Fbxo7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbxo7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631128	M	MP:0005505	thrombocytosis	Fbxo7<tm1a(EUCOMM)Wtsi>/Fbxo7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbxo7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631128	F	MP:0010088	decreased circulating fructosamine level	Fbxo7<tm1a(EUCOMM)Wtsi>/Fbxo7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbxo7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631128	M	MP:0005344	increased circulating bilirubin level	Fbxo7<tm1a(EUCOMM)Wtsi>/Fbxo7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbxo7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631133	F	MP:0000111	cleft palate	Fgf9<tm1b(KOMP)Wtsi>/Fgf9<tm1b(KOMP)Wtsi>	C57BL/6N-Fgf9<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631137	F	MP:0010123	increased bone mineral content	Fnbp1l<tm1.1(KOMP)Vlcg>/Fnbp1l<tm1.1(KOMP)Vlcg>	C57BL/6N-Fnbp1l<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631137	F	MP:0011110	preweaning lethality, incomplete penetrance	Fnbp1l<tm1.1(KOMP)Vlcg>/Fnbp1l<tm1.1(KOMP)Vlcg>	C57BL/6N-Fnbp1l<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631137	M	MP:0002175	decreased brain weight	Fnbp1l<tm1.1(KOMP)Vlcg>/Fnbp1l<tm1.1(KOMP)Vlcg>	C57BL/6N-Fnbp1l<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631138	F	MP:0009142	decreased prepulse inhibition	Foxo3<tm1.1(KOMP)Vlcg>/Foxo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxo3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631138	M	MP:0001402	decreased locomotor activity	Foxo3<tm1.1(KOMP)Vlcg>/Foxo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxo3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631138	M	MP:0005561	increased mean corpuscular hemoglobin	Foxo3<tm1.1(KOMP)Vlcg>/Foxo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxo3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631138	M	MP:0002590	increased mean corpuscular volume	Foxo3<tm1.1(KOMP)Vlcg>/Foxo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxo3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631138	M	MP:0005293	impaired glucose tolerance	Foxo3<tm1.1(KOMP)Vlcg>/Foxo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxo3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631138	M	MP:0003179	thrombocytopenia	Foxo3<tm1.1(KOMP)Vlcg>/Foxo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxo3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631138	M	MP:0002875	decreased erythrocyte cell number	Foxo3<tm1.1(KOMP)Vlcg>/Foxo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxo3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631138	F	MP:0002833	increased heart weight	Foxo3<tm1.1(KOMP)Vlcg>/Foxo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxo3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631138	M	MP:0000063	decreased bone mineral density	Foxo3<tm1.1(KOMP)Vlcg>/Foxo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxo3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631138	F	MP:0003020	decreased circulating chloride level	Foxo3<tm1.1(KOMP)Vlcg>/Foxo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxo3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631138	M	MP:0012121	sclerocornea	Foxo3<tm1.1(KOMP)Vlcg>/Foxo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxo3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631138	F	MP:0011396	abnormal sleep behavior	Foxo3<tm1.1(KOMP)Vlcg>/Foxo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxo3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631166	M	MP:0005343	increased circulating aspartate transaminase level	Ghrhr<tm1.1(KOMP)Vlcg>/Ghrhr<+>	C57BL/6N-Ghrhr<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631166	F	MP:0001399	hyperactivity	Ghrhr<tm1.1(KOMP)Vlcg>/Ghrhr<+>	C57BL/6N-Ghrhr<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631166	M	MP:0002941	increased circulating alanine transaminase level	Ghrhr<tm1.1(KOMP)Vlcg>/Ghrhr<+>	C57BL/6N-Ghrhr<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631167	F	MP:0011396	abnormal sleep behavior	Gimap6<tm1b(KOMP)Wtsi>/Gimap6<tm1b(KOMP)Wtsi>	C57BL/6N-Gimap6<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631167	F	MP:0002968	increased circulating alkaline phosphatase level	Gimap6<tm1b(KOMP)Wtsi>/Gimap6<tm1b(KOMP)Wtsi>	C57BL/6N-Gimap6<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631167	F	MP:0001556	increased circulating HDL cholesterol level	Gimap6<tm1b(KOMP)Wtsi>/Gimap6<tm1b(KOMP)Wtsi>	C57BL/6N-Gimap6<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631167	F	MP:0013279	increased fasting circulating glucose level	Gimap6<tm1b(KOMP)Wtsi>/Gimap6<tm1b(KOMP)Wtsi>	C57BL/6N-Gimap6<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631167	M	MP:0005560	decreased circulating glucose level	Gimap6<tm1b(KOMP)Wtsi>/Gimap6<tm1b(KOMP)Wtsi>	C57BL/6N-Gimap6<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631167	M	MP:0000194	increased circulating calcium level	Gimap6<tm1b(KOMP)Wtsi>/Gimap6<tm1b(KOMP)Wtsi>	C57BL/6N-Gimap6<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631167	F	MP:0004151	decreased circulating iron level	Gimap6<tm1b(KOMP)Wtsi>/Gimap6<tm1b(KOMP)Wtsi>	C57BL/6N-Gimap6<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631167	F	MP:0005633	increased circulating sodium level	Gimap6<tm1b(KOMP)Wtsi>/Gimap6<tm1b(KOMP)Wtsi>	C57BL/6N-Gimap6<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631167	F	MP:0002591	decreased mean corpuscular volume	Gimap6<tm1b(KOMP)Wtsi>/Gimap6<tm1b(KOMP)Wtsi>	C57BL/6N-Gimap6<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631173	F	MP:0008806	increased circulating amylase level	Glt8d2<tm1a(KOMP)Wtsi>/Glt8d2<tm1a(KOMP)Wtsi>	C57BL/6N-Glt8d2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631173	M	MP:0002079	increased circulating insulin level	Glt8d2<tm1a(KOMP)Wtsi>/Glt8d2<tm1a(KOMP)Wtsi>	C57BL/6N-Glt8d2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631174	F	MP:0011396	abnormal sleep behavior	Glycam1<tm1.1(KOMP)Vlcg>/Glycam1<+>	C57BL/6N-Glycam1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631175	F	MP:0001399	hyperactivity	Glycam1<tm1.1(KOMP)Vlcg>/Glycam1<tm1.1(KOMP)Vlcg>	C57BL/6N-Glycam1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631183	M	MP:0013279	increased fasting circulating glucose level	Gpnmb<tm1.1(KOMP)Vlcg>/Gpnmb<+>	C57BL/6N-Gpnmb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631196	M	MP:0005633	increased circulating sodium level	H1f10<tm1.1(KOMP)Vlcg>/H1f10<+>	C57BL/6N-H1f10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631196	F	MP:0001399	hyperactivity	H1f10<tm1.1(KOMP)Vlcg>/H1f10<+>	C57BL/6N-H1f10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631196	F	MP:0000955	abnormal spinal cord morphology	H1f10<tm1.1(KOMP)Vlcg>/H1f10<+>	C57BL/6N-H1f10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631197	M	MP:0005561	increased mean corpuscular hemoglobin	H1f10<tm1.1(KOMP)Vlcg>/H1f10<tm1.1(KOMP)Vlcg>	C57BL/6N-H1f10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631197	F	MP:0013279	increased fasting circulating glucose level	H1f10<tm1.1(KOMP)Vlcg>/H1f10<tm1.1(KOMP)Vlcg>	C57BL/6N-H1f10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631197	F	MP:0002152	abnormal brain morphology	H1f10<tm1.1(KOMP)Vlcg>/H1f10<tm1.1(KOMP)Vlcg>	C57BL/6N-H1f10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631200	F	MP:0002968	increased circulating alkaline phosphatase level	Hdac10<tm1.1(KOMP)Mbp>/Hdac10<tm1.1(KOMP)Mbp>	C57BL/6N-Hdac10<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631203	F	MP:0009141	increased prepulse inhibition	Hjv<tm1b(KOMP)Wtsi>/Hjv<tm1b(KOMP)Wtsi>	C57BL/6N-Hjv<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631203	M	MP:0005564	increased hemoglobin content	Hjv<tm1b(KOMP)Wtsi>/Hjv<tm1b(KOMP)Wtsi>	C57BL/6N-Hjv<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631206	F	MP:0001697	abnormal embryo size	Hsf1<tm1.1(KOMP)Vlcg>/Hsf1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsf1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631207	F	MP:0001556	increased circulating HDL cholesterol level	Hspa5<tm1.1(KOMP)Vlcg>/Hspa5<+>	C57BL/6N-Hspa5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631207	M	MP:0003020	decreased circulating chloride level	Hspa5<tm1.1(KOMP)Vlcg>/Hspa5<+>	C57BL/6N-Hspa5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631207	F	MP:0005178	increased circulating cholesterol level	Hspa5<tm1.1(KOMP)Vlcg>/Hspa5<+>	C57BL/6N-Hspa5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631209	F	MP:0002804	abnormal motor learning	Hspb2<tm1.1(KOMP)Vlcg>/Hspb2<tm1.1(KOMP)Vlcg>	C57BL/6N-Hspb2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631209	F	MP:0002833	increased heart weight	Hspb2<tm1.1(KOMP)Vlcg>/Hspb2<tm1.1(KOMP)Vlcg>	C57BL/6N-Hspb2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631210	M	MP:0010053	decreased grip strength	Htr1b<tm1.1(KOMP)Vlcg>/Htr1b<+>	C57BL/6N-Htr1b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631210	M	MP:0003960	increased lean body mass	Htr1b<tm1.1(KOMP)Vlcg>/Htr1b<+>	C57BL/6N-Htr1b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631210	M	MP:0010025	decreased total body fat amount	Htr1b<tm1.1(KOMP)Vlcg>/Htr1b<+>	C57BL/6N-Htr1b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631217	F	MP:0013279	increased fasting circulating glucose level	Igsf11<tm1b(KOMP)Wtsi>/Igsf11<tm1b(KOMP)Wtsi>	C57BL/6N-Igsf11<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631217	M	MP:0001399	hyperactivity	Igsf11<tm1b(KOMP)Wtsi>/Igsf11<tm1b(KOMP)Wtsi>	C57BL/6N-Igsf11<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631217	M	MP:0001925	male infertility	Igsf11<tm1b(KOMP)Wtsi>/Igsf11<tm1b(KOMP)Wtsi>	C57BL/6N-Igsf11<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631230	M	MP:0001925	male infertility	Iqub<tm1.1(KOMP)Vlcg>/Iqub<tm1.1(KOMP)Vlcg>	C57BL/6N-Iqub<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631231	F	MP:0002875	decreased erythrocyte cell number	Irf8<tm1b(KOMP)Wtsi>/Irf8<tm1b(KOMP)Wtsi>	C57BL/6N-Irf8<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631231	F	MP:0002590	increased mean corpuscular volume	Irf8<tm1b(KOMP)Wtsi>/Irf8<tm1b(KOMP)Wtsi>	C57BL/6N-Irf8<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631231	M	MP:0013278	decreased fasting circulating glucose level	Irf8<tm1b(KOMP)Wtsi>/Irf8<tm1b(KOMP)Wtsi>	C57BL/6N-Irf8<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631232	F	MP:0000194	increased circulating calcium level	Itga8<tm1b(KOMP)Wtsi>/Itga8<+>	C57BL/6N-Itga8<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631232	F	MP:0005560	decreased circulating glucose level	Itga8<tm1b(KOMP)Wtsi>/Itga8<+>	C57BL/6N-Itga8<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631232	F	MP:0005633	increased circulating sodium level	Itga8<tm1b(KOMP)Wtsi>/Itga8<+>	C57BL/6N-Itga8<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631232	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Itga8<tm1b(KOMP)Wtsi>/Itga8<+>	C57BL/6N-Itga8<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631232	F	MP:0001554	increased circulating free fatty acids level	Itga8<tm1b(KOMP)Wtsi>/Itga8<+>	C57BL/6N-Itga8<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631233	F	MP:0000266	abnormal heart morphology	Itsn2<tm1.1(KOMP)Vlcg>/Itsn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Itsn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631233	F	MP:0000367	abnormal coat/ hair morphology	Itsn2<tm1.1(KOMP)Vlcg>/Itsn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Itsn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631233	F	MP:0000274	enlarged heart	Itsn2<tm1.1(KOMP)Vlcg>/Itsn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Itsn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631233	M	MP:0001415	increased exploration in new environment	Itsn2<tm1.1(KOMP)Vlcg>/Itsn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Itsn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631235	M	MP:0001925	male infertility	Jam3<tm1.1(KOMP)Vlcg>/Jam3<tm1.1(KOMP)Vlcg>	C57BL/6N-Jam3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631236	M	MP:0005564	increased hemoglobin content	Kcnh3<tm1.1(KOMP)Vlcg>/Kcnh3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnh3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631236	F	MP:0001399	hyperactivity	Kcnh3<tm1.1(KOMP)Vlcg>/Kcnh3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnh3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631236	F	MP:0013279	increased fasting circulating glucose level	Kcnh3<tm1.1(KOMP)Vlcg>/Kcnh3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnh3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631236	M	MP:0001325	abnormal retina morphology	Kcnh3<tm1.1(KOMP)Vlcg>/Kcnh3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnh3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631239	F	MP:0001488	increased startle reflex	Kif1b<tm1b(KOMP)Wtsi>/Kif1b<+>	C57BL/6N-Kif1b<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631239	F	MP:0002574	increased vertical activity	Kif1b<tm1b(KOMP)Wtsi>/Kif1b<+>	C57BL/6N-Kif1b<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631239	F	MP:0001399	hyperactivity	Kif1b<tm1b(KOMP)Wtsi>/Kif1b<+>	C57BL/6N-Kif1b<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631239	F	MP:0005566	decreased blood urea nitrogen level	Kif1b<tm1b(KOMP)Wtsi>/Kif1b<+>	C57BL/6N-Kif1b<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631239	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Kif1b<tm1b(KOMP)Wtsi>/Kif1b<+>	C57BL/6N-Kif1b<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631239	F	MP:0003019	increased circulating chloride level	Kif1b<tm1b(KOMP)Wtsi>/Kif1b<+>	C57BL/6N-Kif1b<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631240	M	MP:0002833	increased heart weight	Kif26b<tm2b(KOMP)Wtsi>/Kif26b<+>	C57BL/6N-Kif26b<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631240	F	MP:0002702	decreased circulating free fatty acids level	Kif26b<tm2b(KOMP)Wtsi>/Kif26b<+>	C57BL/6N-Kif26b<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631240	F	MP:0001399	hyperactivity	Kif26b<tm2b(KOMP)Wtsi>/Kif26b<+>	C57BL/6N-Kif26b<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631244	F	MP:0001554	increased circulating free fatty acids level	Klc2<tm1e(EUCOMM)Wtsi>/Klc2<tm1e(EUCOMM)Wtsi>	C57BL/6N-Klc2<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631248	F	MP:0002874	decreased hemoglobin content	Klhl18<tm1a(KOMP)Wtsi>/Klhl18<tm1a(KOMP)Wtsi>	C57BL/6N-Klhl18<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631248	M	MP:0010092	increased circulating magnesium level	Klhl18<tm1a(KOMP)Wtsi>/Klhl18<tm1a(KOMP)Wtsi>	C57BL/6N-Klhl18<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631248	F	MP:0000208	decreased hematocrit	Klhl18<tm1a(KOMP)Wtsi>/Klhl18<tm1a(KOMP)Wtsi>	C57BL/6N-Klhl18<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631248	F	MP:0002875	decreased erythrocyte cell number	Klhl18<tm1a(KOMP)Wtsi>/Klhl18<tm1a(KOMP)Wtsi>	C57BL/6N-Klhl18<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631248	M	MP:0010052	increased grip strength	Klhl18<tm1a(KOMP)Wtsi>/Klhl18<tm1a(KOMP)Wtsi>	C57BL/6N-Klhl18<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631262	M	MP:0003443	increased circulating glycerol level	Lgals7<tm1a(EUCOMM)Wtsi>/Lgals7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Lgals7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631262	M	MP:0001554	increased circulating free fatty acids level	Lgals7<tm1a(EUCOMM)Wtsi>/Lgals7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Lgals7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631270	F	MP:0000194	increased circulating calcium level	Lonrf3<tm1a(KOMP)Wtsi>/Lonrf3<tm1a(KOMP)Wtsi>	C57BL/6N-Lonrf3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631273	F	MP:0005567	decreased circulating total protein level	Loxl1<tm1.1(KOMP)Vlcg>/Loxl1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Loxl1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631276	F	MP:0002833	increased heart weight	Lrp1<tm1.1(KOMP)Wtsi>/Lrp1<+>	C57BL/6N-Lrp1<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631278	M	MP:0005292	improved glucose tolerance	Lrrc15<tm1b(KOMP)Wtsi>/Lrrc15<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrc15<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631283	F	MP:0005565	increased blood urea nitrogen level	Lypd6b<tm1b(KOMP)Wtsi>/Lypd6b<tm1b(KOMP)Wtsi>	C57BL/6N-Lypd6b<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631283	M	MP:0005419	decreased circulating serum albumin level	Lypd6b<tm1b(KOMP)Wtsi>/Lypd6b<tm1b(KOMP)Wtsi>	C57BL/6N-Lypd6b<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631283	M	MP:0000198	decreased circulating phosphate level	Lypd6b<tm1b(KOMP)Wtsi>/Lypd6b<tm1b(KOMP)Wtsi>	C57BL/6N-Lypd6b<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631297	M	MP:0000062	increased bone mineral density	Mast2<tm1a(KOMP)Wtsi>/Mast2<tm1a(KOMP)Wtsi>	C57BL/6N-Mast2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631300	M	MP:0005633	increased circulating sodium level	Mdk<tm1.1(KOMP)Mbp>/Mdk<+>	C57BL/6N-Mdk<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631300	M	MP:0003019	increased circulating chloride level	Mdk<tm1.1(KOMP)Mbp>/Mdk<+>	C57BL/6N-Mdk<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631313	M	MP:0002833	increased heart weight	Mmp8<tm1.1(KOMP)Vlcg>/Mmp8<tm1.1(KOMP)Vlcg>	C57BL/6N-Mmp8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631316	M	MP:0001488	increased startle reflex	Moxd1<tm2b(KOMP)Wtsi>/Moxd1<tm2b(KOMP)Wtsi>	C57BL/6N-Moxd1<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631317	M	MP:0002833	increased heart weight	Mrps25<tm1.1(KOMP)Vlcg>/Mrps25<+>	C57BL/6N-Mrps25<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631317	F	MP:0000195	decreased circulating calcium level	Mrps25<tm1.1(KOMP)Vlcg>/Mrps25<+>	C57BL/6N-Mrps25<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631317	M	MP:0005633	increased circulating sodium level	Mrps25<tm1.1(KOMP)Vlcg>/Mrps25<+>	C57BL/6N-Mrps25<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631321	M	MP:0001575	cyanosis	Msx1<tm1b(KOMP)Wtsi>/Msx1<tm1b(KOMP)Wtsi>	C57BL/6N-Msx1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631324	M	MP:0005559	increased circulating glucose level	Mtss2<tm1a(KOMP)Wtsi>/Mtss2<tm1a(KOMP)Wtsi>	C57BL/6N-tss2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631328	F	MP:0001304	cataract	Myo15a<tm1a(EUCOMM)Wtsi>/Myo15a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Myo15a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631328	M	MP:0010024	increased total body fat amount	Myo15a<tm1a(EUCOMM)Wtsi>/Myo15a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Myo15a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631328	F	MP:0001303	abnormal lens morphology	Myo15a<tm1a(EUCOMM)Wtsi>/Myo15a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Myo15a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631328	F	MP:0010052	increased grip strength	Myo15a<tm1a(EUCOMM)Wtsi>/Myo15a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Myo15a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631331	F	MP:0008810	increased circulating iron level	Naaa<tm1a(KOMP)Wtsi>/Naaa<tm1a(KOMP)Wtsi>	C57BL/6N-Naaa<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631331	F	MP:0002875	decreased erythrocyte cell number	Naaa<tm1a(KOMP)Wtsi>/Naaa<tm1a(KOMP)Wtsi>	C57BL/6N-Naaa<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631331	F	MP:0000208	decreased hematocrit	Naaa<tm1a(KOMP)Wtsi>/Naaa<tm1a(KOMP)Wtsi>	C57BL/6N-Naaa<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631331	F	MP:0002874	decreased hemoglobin content	Naaa<tm1a(KOMP)Wtsi>/Naaa<tm1a(KOMP)Wtsi>	C57BL/6N-Naaa<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631338	M	MP:0004924	abnormal behavior	Ncald<tm1.1(KOMP)Vlcg>/Ncald<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncald<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631338	F	MP:0002968	increased circulating alkaline phosphatase level	Ncald<tm1.1(KOMP)Vlcg>/Ncald<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncald<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631338	F	MP:0010097	abnormal retina blood vessel morphology	Ncald<tm1.1(KOMP)Vlcg>/Ncald<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncald<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631338	F	MP:0000063	decreased bone mineral density	Ncald<tm1.1(KOMP)Vlcg>/Ncald<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncald<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631338	F	MP:0002792	abnormal retina vasculature morphology	Ncald<tm1.1(KOMP)Vlcg>/Ncald<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncald<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631338	M	MP:0003063	increased coping response	Ncald<tm1.1(KOMP)Vlcg>/Ncald<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncald<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631338	F	MP:0009142	decreased prepulse inhibition	Ncald<tm1.1(KOMP)Vlcg>/Ncald<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncald<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631338	F	MP:0003795	abnormal bone structure	Ncald<tm1.1(KOMP)Vlcg>/Ncald<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncald<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631338	F	MP:0010124	decreased bone mineral content	Ncald<tm1.1(KOMP)Vlcg>/Ncald<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncald<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631338	F	MP:0001319	irregularly shaped pupil	Ncald<tm1.1(KOMP)Vlcg>/Ncald<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncald<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631338	F	MP:0006243	impaired pupillary reflex	Ncald<tm1.1(KOMP)Vlcg>/Ncald<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncald<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631338	F	MP:0005565	increased blood urea nitrogen level	Ncald<tm1.1(KOMP)Vlcg>/Ncald<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncald<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631347	M	MP:0003960	increased lean body mass	Ninj2<tm1a(KOMP)Wtsi>/Ninj2<tm1a(KOMP)Wtsi>	C57BL/6N-Ninj2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631347	M	MP:0010123	increased bone mineral content	Ninj2<tm1a(KOMP)Wtsi>/Ninj2<tm1a(KOMP)Wtsi>	C57BL/6N-Ninj2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631347	M	MP:0010067	increased red blood cell distribution width	Ninj2<tm1a(KOMP)Wtsi>/Ninj2<tm1a(KOMP)Wtsi>	C57BL/6N-Ninj2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631347	F	MP:0000194	increased circulating calcium level	Ninj2<tm1a(KOMP)Wtsi>/Ninj2<tm1a(KOMP)Wtsi>	C57BL/6N-Ninj2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631353	M	MP:0001325	abnormal retina morphology	Nsf<tm1b(KOMP)Mbp>/Nsf<+>	C57BL/6N-Nsf<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631353	F	MP:0005564	increased hemoglobin content	Nsf<tm1b(KOMP)Mbp>/Nsf<+>	C57BL/6N-Nsf<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631353	M	MP:0000186	decreased circulating HDL cholesterol level	Nsf<tm1b(KOMP)Mbp>/Nsf<+>	C57BL/6N-Nsf<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631353	M	MP:0005560	decreased circulating glucose level	Nsf<tm1b(KOMP)Mbp>/Nsf<+>	C57BL/6N-Nsf<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631363	M	MP:0005560	decreased circulating glucose level	Ocstamp<tm2b(KOMP)Wtsi>/Ocstamp<tm2b(KOMP)Wtsi>	C57BL/6N-Ocstamp<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631363	F	MP:0002968	increased circulating alkaline phosphatase level	Ocstamp<tm2b(KOMP)Wtsi>/Ocstamp<tm2b(KOMP)Wtsi>	C57BL/6N-Ocstamp<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631367	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Olah<tm1b(KOMP)Wtsi>/Olah<tm1b(KOMP)Wtsi>	C57BL/6N-Olah<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631367	F	MP:0002590	increased mean corpuscular volume	Olah<tm1b(KOMP)Wtsi>/Olah<tm1b(KOMP)Wtsi>	C57BL/6N-Olah<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631372	M	MP:0004609	vertebral fusion	Os9<tm1a(EUCOMM)Wtsi>/Os9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Os9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631373	M	MP:0002874	decreased hemoglobin content	Osm<tm1b(KOMP)Wtsi>/Osm<tm1b(KOMP)Wtsi>	C57BL/6N-Osm<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631373	M	MP:0005560	decreased circulating glucose level	Osm<tm1b(KOMP)Wtsi>/Osm<tm1b(KOMP)Wtsi>	C57BL/6N-Osm<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631373	M	MP:0010123	increased bone mineral content	Osm<tm1b(KOMP)Wtsi>/Osm<tm1b(KOMP)Wtsi>	C57BL/6N-Osm<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631373	M	MP:0002833	increased heart weight	Osm<tm1b(KOMP)Wtsi>/Osm<tm1b(KOMP)Wtsi>	C57BL/6N-Osm<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631373	M	MP:0000208	decreased hematocrit	Osm<tm1b(KOMP)Wtsi>/Osm<tm1b(KOMP)Wtsi>	C57BL/6N-Osm<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631374	M	MP:0001488	increased startle reflex	Otoa<tm1.1(KOMP)Vlcg>/Otoa<tm1.1(KOMP)Vlcg>	C57BL/6N-Otoa<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631374	F	MP:0005562	decreased mean corpuscular hemoglobin	Otoa<tm1.1(KOMP)Vlcg>/Otoa<tm1.1(KOMP)Vlcg>	C57BL/6N-Otoa<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631375	F	MP:0002098	abnormal vibrissa morphology	Ovol1<tm1b(KOMP)Wtsi>/Ovol1<+>	C57BL/6N-Ovol1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631375	F	MP:0000208	decreased hematocrit	Ovol1<tm1b(KOMP)Wtsi>/Ovol1<+>	C57BL/6N-Ovol1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631375	F	MP:0002875	decreased erythrocyte cell number	Ovol1<tm1b(KOMP)Wtsi>/Ovol1<+>	C57BL/6N-Ovol1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631375	F	MP:0002874	decreased hemoglobin content	Ovol1<tm1b(KOMP)Wtsi>/Ovol1<+>	C57BL/6N-Ovol1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631375	F	MP:0003179	thrombocytopenia	Ovol1<tm1b(KOMP)Wtsi>/Ovol1<+>	C57BL/6N-Ovol1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631377	F	MP:0001926	female infertility	Pabpn1l<tm1a(EUCOMM)Wtsi>/Pabpn1l<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pabpn1l<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631383	F	MP:0002833	increased heart weight	Parp8<tm1.1(KOMP)Wtsi>/Parp8<tm1.1(KOMP)Wtsi>	C57BL/6N-Parp8<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631383	F	MP:0001417	decreased exploration in new environment	Parp8<tm1.1(KOMP)Wtsi>/Parp8<tm1.1(KOMP)Wtsi>	C57BL/6N-Parp8<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631383	F	MP:0003064	decreased coping response	Parp8<tm1.1(KOMP)Wtsi>/Parp8<tm1.1(KOMP)Wtsi>	C57BL/6N-Parp8<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631386	M	MP:0002644	decreased circulating triglyceride level	Pax7<tm1.1(KOMP)Vlcg>/Pax7<+>	C57BL/6N-Pax7<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631393	F	MP:0005650	abnormal limb bud morphology	Pcsk5<tm1b(KOMP)Mbp>/Pcsk5<tm1b(KOMP)Mbp>	C57BL/6N-Pcsk5<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631400	M	MP:0005419	decreased circulating serum albumin level	Pear1<tm1a(KOMP)Wtsi>/Pear1<tm1a(KOMP)Wtsi>	C57BL/6N-Pear1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631401	M	MP:0002175	decreased brain weight	Peli1<tm1b(EUCOMM)Wtsi>/Peli1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Peli1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5631401	M	MP:0004952	increased spleen weight	Peli1<tm1b(EUCOMM)Wtsi>/Peli1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Peli1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5631401	M	MP:0005292	improved glucose tolerance	Peli1<tm1b(EUCOMM)Wtsi>/Peli1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Peli1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5631401	M	MP:0000274	enlarged heart	Peli1<tm1b(EUCOMM)Wtsi>/Peli1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Peli1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5631401	M	MP:0003960	increased lean body mass	Peli1<tm1b(EUCOMM)Wtsi>/Peli1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Peli1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5631401	M	MP:0000219	increased neutrophil cell number	Peli1<tm1b(EUCOMM)Wtsi>/Peli1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Peli1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5631404	F	MP:0001926	female infertility	Pfkfb4<tm1b(KOMP)Wtsi>/Pfkfb4<tm1b(KOMP)Wtsi>	C57BL/6N-Pfkfb4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631404	M	MP:0001529	abnormal vocalization	Pfkfb4<tm1b(KOMP)Wtsi>/Pfkfb4<tm1b(KOMP)Wtsi>	C57BL/6N-Pfkfb4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631404	M	MP:0006203	eye hemorrhage	Pfkfb4<tm1b(KOMP)Wtsi>/Pfkfb4<tm1b(KOMP)Wtsi>	C57BL/6N-Pfkfb4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631406	M	MP:0002151	abnormal neural tube morphology	Pibf1<tm1.1(KOMP)Vlcg>/Pibf1<tm1.1(KOMP)Vlcg>	C57BL/6N-Pibf1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631407	M	MP:0010052	increased grip strength	Pigh<tm1.1(KOMP)Vlcg>/Pigh<+>	C57BL/6N-Pigh<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631407	M	MP:0000186	decreased circulating HDL cholesterol level	Pigh<tm1.1(KOMP)Vlcg>/Pigh<+>	C57BL/6N-Pigh<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631413	M	MP:0013279	increased fasting circulating glucose level	Pitx3<tm1.1(KOMP)Vlcg>/Pitx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Pitx3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631413	M	MP:0010052	increased grip strength	Pitx3<tm1.1(KOMP)Vlcg>/Pitx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Pitx3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631413	F	MP:0002626	increased heart rate	Pitx3<tm1.1(KOMP)Vlcg>/Pitx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Pitx3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631413	F	MP:0001516	abnormal motor coordination/balance	Pitx3<tm1.1(KOMP)Vlcg>/Pitx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Pitx3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631413	M	MP:0010571	shortened ST segment	Pitx3<tm1.1(KOMP)Vlcg>/Pitx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Pitx3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631413	M	MP:0005560	decreased circulating glucose level	Pitx3<tm1.1(KOMP)Vlcg>/Pitx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Pitx3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631415	M	MP:0001529	abnormal vocalization	Plcb2<tm1b(KOMP)Wtsi>/Plcb2<tm1b(KOMP)Wtsi>	C57BL/6N-Plcb2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631415	M	MP:0001925	male infertility	Plcb2<tm1b(KOMP)Wtsi>/Plcb2<tm1b(KOMP)Wtsi>	C57BL/6N-Plcb2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631415	F	MP:0000689	abnormal spleen morphology	Plcb2<tm1b(KOMP)Wtsi>/Plcb2<tm1b(KOMP)Wtsi>	C57BL/6N-Plcb2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631415	F	MP:0000691	enlarged spleen	Plcb2<tm1b(KOMP)Wtsi>/Plcb2<tm1b(KOMP)Wtsi>	C57BL/6N-Plcb2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631422	F	MP:0005561	increased mean corpuscular hemoglobin	Pls3<tm1a(EUCOMM)Wtsi>/Pls3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pls3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631422	F	MP:0002968	increased circulating alkaline phosphatase level	Pls3<tm1a(EUCOMM)Wtsi>/Pls3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pls3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631433	M	MP:0001402	decreased locomotor activity	Saxo4<tm1b(KOMP)Wtsi>/Saxo4<tm1b(KOMP)Wtsi>	C57BL/6N-Saxo4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631434	M	MP:0002574	increased vertical activity	Ppp1r9b<tm1.1(KOMP)Vlcg>/Ppp1r9b<tm1.1(KOMP)Vlcg>	C57BL/6N-Ppp1r9b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631434	F	MP:0005343	increased circulating aspartate transaminase level	Ppp1r9b<tm1.1(KOMP)Vlcg>/Ppp1r9b<tm1.1(KOMP)Vlcg>	C57BL/6N-Ppp1r9b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631434	F	MP:0002941	increased circulating alanine transaminase level	Ppp1r9b<tm1.1(KOMP)Vlcg>/Ppp1r9b<tm1.1(KOMP)Vlcg>	C57BL/6N-Ppp1r9b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631434	F	MP:0003795	abnormal bone structure	Ppp1r9b<tm1.1(KOMP)Vlcg>/Ppp1r9b<tm1.1(KOMP)Vlcg>	C57BL/6N-Ppp1r9b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631440	F	MP:0005344	increased circulating bilirubin level	Prelp<tm1.1(KOMP)Vlcg>/Prelp<tm1.1(KOMP)Vlcg>	C57BL/6N-Prelp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631440	F	MP:0001258	decreased body length	Prelp<tm1.1(KOMP)Vlcg>/Prelp<tm1.1(KOMP)Vlcg>	C57BL/6N-Prelp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631440	F	MP:0000194	increased circulating calcium level	Prelp<tm1.1(KOMP)Vlcg>/Prelp<tm1.1(KOMP)Vlcg>	C57BL/6N-Prelp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631441	M	MP:0002702	decreased circulating free fatty acids level	Prep<tm1b(KOMP)Wtsi>/Prep<+>	C57BL/6N-Prep<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631441	M	MP:0005627	increased circulating potassium level	Prep<tm1b(KOMP)Wtsi>/Prep<+>	C57BL/6N-Prep<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631441	M	MP:0020870	decreased thigmotaxis	Prep<tm1b(KOMP)Wtsi>/Prep<+>	C57BL/6N-Prep<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631443	M	MP:0001529	abnormal vocalization	Prodh<tm1b(KOMP)Wtsi>/Prodh<tm1b(KOMP)Wtsi>	C57BL/6N-Prodh<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631443	M	MP:0002764	short tibia	Prodh<tm1b(KOMP)Wtsi>/Prodh<tm1b(KOMP)Wtsi>	C57BL/6N-Prodh<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631445	F	MP:0001325	abnormal retina morphology	Prom2<tm1.1(KOMP)Vlcg>/Prom2<tm1.1(KOMP)Vlcg>	C57BL/6N-Prom2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631445	M	MP:0010053	decreased grip strength	Prom2<tm1.1(KOMP)Vlcg>/Prom2<tm1.1(KOMP)Vlcg>	C57BL/6N-Prom2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631445	F	MP:0001399	hyperactivity	Prom2<tm1.1(KOMP)Vlcg>/Prom2<tm1.1(KOMP)Vlcg>	C57BL/6N-Prom2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631445	F	MP:0005564	increased hemoglobin content	Prom2<tm1.1(KOMP)Vlcg>/Prom2<tm1.1(KOMP)Vlcg>	C57BL/6N-Prom2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631445	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Prom2<tm1.1(KOMP)Vlcg>/Prom2<tm1.1(KOMP)Vlcg>	C57BL/6N-Prom2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631445	F	MP:0011396	abnormal sleep behavior	Prom2<tm1.1(KOMP)Vlcg>/Prom2<tm1.1(KOMP)Vlcg>	C57BL/6N-Prom2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631445	M	MP:0000579	abnormal nail morphology	Prom2<tm1.1(KOMP)Vlcg>/Prom2<tm1.1(KOMP)Vlcg>	C57BL/6N-Prom2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631452	M	MP:0000195	decreased circulating calcium level	Pth<tm1a(EUCOMM)Wtsi>/Pth<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pth<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631459	F	MP:0001513	limb grasping	Rab15<tm1a(KOMP)Wtsi>/Rab15<tm1a(KOMP)Wtsi>	C57BL/6N-Rab15<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631459	M	MP:0002727	decreased circulating insulin level	Rab15<tm1a(KOMP)Wtsi>/Rab15<tm1a(KOMP)Wtsi>	C57BL/6N-Rab15<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631461	M	MP:0005179	decreased circulating cholesterol level	Rab36<tm1b(KOMP)Wtsi>/Rab36<tm1b(KOMP)Wtsi>	C57BL/6N-Rab36<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631461	F	MP:0000432	abnormal head morphology	Rab36<tm1b(KOMP)Wtsi>/Rab36<tm1b(KOMP)Wtsi>	C57BL/6N-Rab36<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631461	F	MP:0005278	abnormal cholesterol homeostasis	Rab36<tm1b(KOMP)Wtsi>/Rab36<tm1b(KOMP)Wtsi>	C57BL/6N-Rab36<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631461	F	MP:0005419	decreased circulating serum albumin level	Rab36<tm1b(KOMP)Wtsi>/Rab36<tm1b(KOMP)Wtsi>	C57BL/6N-Rab36<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631463	M	MP:0002833	increased heart weight	Rab43<tm1.1(KOMP)Vlcg>/Rab43<tm1.1(KOMP)Vlcg>	C57BL/6N-Rab43<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631463	F	MP:0005561	increased mean corpuscular hemoglobin	Rab43<tm1.1(KOMP)Vlcg>/Rab43<tm1.1(KOMP)Vlcg>	C57BL/6N-Rab43<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631463	F	MP:0013278	decreased fasting circulating glucose level	Rab43<tm1.1(KOMP)Vlcg>/Rab43<tm1.1(KOMP)Vlcg>	C57BL/6N-Rab43<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631464	M	MP:0005633	increased circulating sodium level	Rab5a<tm1b(KOMP)Wtsi>/Rab5a<tm1b(KOMP)Wtsi>	C57BL/6N-Rab5a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631464	M	MP:0005627	increased circulating potassium level	Rab5a<tm1b(KOMP)Wtsi>/Rab5a<tm1b(KOMP)Wtsi>	C57BL/6N-Rab5a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631464	M	MP:0001325	abnormal retina morphology	Rab5a<tm1b(KOMP)Wtsi>/Rab5a<tm1b(KOMP)Wtsi>	C57BL/6N-Rab5a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631464	M	MP:0000186	decreased circulating HDL cholesterol level	Rab5a<tm1b(KOMP)Wtsi>/Rab5a<tm1b(KOMP)Wtsi>	C57BL/6N-Rab5a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631464	M	MP:0003131	increased erythrocyte cell number	Rab5a<tm1b(KOMP)Wtsi>/Rab5a<tm1b(KOMP)Wtsi>	C57BL/6N-Rab5a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631464	F	MP:0010053	decreased grip strength	Rab5a<tm1b(KOMP)Wtsi>/Rab5a<tm1b(KOMP)Wtsi>	C57BL/6N-Rab5a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631464	F	MP:0011396	abnormal sleep behavior	Rab5a<tm1b(KOMP)Wtsi>/Rab5a<tm1b(KOMP)Wtsi>	C57BL/6N-Rab5a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631467	M	MP:0001925	male infertility	Rad21l<tm1b(KOMP)Wtsi>/Rad21l<tm1b(KOMP)Wtsi>	C57BL/6N-Rad21l<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631467	M	MP:0005560	decreased circulating glucose level	Rad21l<tm1b(KOMP)Wtsi>/Rad21l<tm1b(KOMP)Wtsi>	C57BL/6N-Rad21l<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631475	F	MP:0001926	female infertility	Rdx<tm1.1(KOMP)Vlcg>/Rdx<tm1.1(KOMP)Vlcg>	C57BL/6N-Rdx<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631479	F	MP:0001556	increased circulating HDL cholesterol level	Resp18<tm1.1(KOMP)Vlcg>/Resp18<+>	C57BL/6N-Resp18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631488	F	MP:0011396	abnormal sleep behavior	Rimklb<tm1.1(KOMP)Vlcg>/Rimklb<tm1.1(KOMP)Vlcg>	C57BL/6N-Rimklb<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631488	M	MP:0001925	male infertility	Rimklb<tm1.1(KOMP)Vlcg>/Rimklb<tm1.1(KOMP)Vlcg>	C57BL/6N-Rimklb<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631488	F	MP:0002833	increased heart weight	Rimklb<tm1.1(KOMP)Vlcg>/Rimklb<tm1.1(KOMP)Vlcg>	C57BL/6N-Rimklb<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631488	F	MP:0010123	increased bone mineral content	Rimklb<tm1.1(KOMP)Vlcg>/Rimklb<tm1.1(KOMP)Vlcg>	C57BL/6N-Rimklb<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631489	M	MP:0005560	decreased circulating glucose level	Rint1<tm1b(KOMP)Wtsi>/Rint1<+>	C57BL/6N-Rint1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631489	F	MP:0002702	decreased circulating free fatty acids level	Rint1<tm1b(KOMP)Wtsi>/Rint1<+>	C57BL/6N-Rint1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631489	F	MP:0000195	decreased circulating calcium level	Rint1<tm1b(KOMP)Wtsi>/Rint1<+>	C57BL/6N-Rint1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631489	F	MP:0005419	decreased circulating serum albumin level	Rint1<tm1b(KOMP)Wtsi>/Rint1<+>	C57BL/6N-Rint1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631491	F	MP:0001284	absent vibrissae	Ripk3<tm1.1(KOMP)Wtsi>/Ripk3<tm1.1(KOMP)Wtsi>	C57BL/6N-Ripk3<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631491	F	MP:0002135	abnormal kidney morphology	Ripk3<tm1.1(KOMP)Wtsi>/Ripk3<tm1.1(KOMP)Wtsi>	C57BL/6N-Ripk3<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631499	M	MP:0000208	decreased hematocrit	Rpa1<tm1b(KOMP)Wtsi>/Rpa1<+>	C57BL/6N-Rpa1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631499	M	MP:0002702	decreased circulating free fatty acids level	Rpa1<tm1b(KOMP)Wtsi>/Rpa1<+>	C57BL/6N-Rpa1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631499	M	MP:0002874	decreased hemoglobin content	Rpa1<tm1b(KOMP)Wtsi>/Rpa1<+>	C57BL/6N-Rpa1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631499	M	MP:0005560	decreased circulating glucose level	Rpa1<tm1b(KOMP)Wtsi>/Rpa1<+>	C57BL/6N-Rpa1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631499	M	MP:0002875	decreased erythrocyte cell number	Rpa1<tm1b(KOMP)Wtsi>/Rpa1<+>	C57BL/6N-Rpa1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631503	F	MP:0005561	increased mean corpuscular hemoglobin	Rrad<tm1.1(KOMP)Vlcg>/Rrad<tm1.1(KOMP)Vlcg>	C57BL/6N-Rrad<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631503	M	MP:0002833	increased heart weight	Rrad<tm1.1(KOMP)Vlcg>/Rrad<tm1.1(KOMP)Vlcg>	C57BL/6N-Rrad<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631503	F	MP:0002968	increased circulating alkaline phosphatase level	Rrad<tm1.1(KOMP)Vlcg>/Rrad<tm1.1(KOMP)Vlcg>	C57BL/6N-Rrad<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631503	F	MP:0010507	shortened RR interval	Rrad<tm1.1(KOMP)Vlcg>/Rrad<tm1.1(KOMP)Vlcg>	C57BL/6N-Rrad<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631520	M	MP:0005633	increased circulating sodium level	Sdha<tm2b(KOMP)Wtsi>/Sdha<+>	C57BL/6N-Sdha<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631520	M	MP:0004924	abnormal behavior	Sdha<tm2b(KOMP)Wtsi>/Sdha<+>	C57BL/6N-Sdha<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631520	M	MP:0001554	increased circulating free fatty acids level	Sdha<tm2b(KOMP)Wtsi>/Sdha<+>	C57BL/6N-Sdha<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631520	M	MP:0020870	decreased thigmotaxis	Sdha<tm2b(KOMP)Wtsi>/Sdha<+>	C57BL/6N-Sdha<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631520	M	MP:0005560	decreased circulating glucose level	Sdha<tm2b(KOMP)Wtsi>/Sdha<+>	C57BL/6N-Sdha<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631527	F	MP:0000063	decreased bone mineral density	Serinc3<tm1a(KOMP)Wtsi>/Serinc3<tm1a(KOMP)Wtsi>	C57BL/6N-Serinc3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631527	F	MP:0010124	decreased bone mineral content	Serinc3<tm1a(KOMP)Wtsi>/Serinc3<tm1a(KOMP)Wtsi>	C57BL/6N-Serinc3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631527	M	MP:0010093	decreased circulating magnesium level	Serinc3<tm1a(KOMP)Wtsi>/Serinc3<tm1a(KOMP)Wtsi>	C57BL/6N-Serinc3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631530	F	MP:0005627	increased circulating potassium level	Setd6<tm1.1(KOMP)Mbp>/Setd6<tm1.1(KOMP)Mbp>	C57BL/6N-Setd6<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631530	F	MP:0012121	sclerocornea	Setd6<tm1.1(KOMP)Mbp>/Setd6<tm1.1(KOMP)Mbp>	C57BL/6N-Setd6<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631530	F	MP:0002591	decreased mean corpuscular volume	Setd6<tm1.1(KOMP)Mbp>/Setd6<tm1.1(KOMP)Mbp>	C57BL/6N-Setd6<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631530	F	MP:0005343	increased circulating aspartate transaminase level	Setd6<tm1.1(KOMP)Mbp>/Setd6<tm1.1(KOMP)Mbp>	C57BL/6N-Setd6<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631530	F	MP:0001926	female infertility	Setd6<tm1.1(KOMP)Mbp>/Setd6<tm1.1(KOMP)Mbp>	C57BL/6N-Setd6<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631530	F	MP:0002941	increased circulating alanine transaminase level	Setd6<tm1.1(KOMP)Mbp>/Setd6<tm1.1(KOMP)Mbp>	C57BL/6N-Setd6<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631530	F	MP:0005562	decreased mean corpuscular hemoglobin	Setd6<tm1.1(KOMP)Mbp>/Setd6<tm1.1(KOMP)Mbp>	C57BL/6N-Setd6<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631530	F	MP:0005344	increased circulating bilirubin level	Setd6<tm1.1(KOMP)Mbp>/Setd6<tm1.1(KOMP)Mbp>	C57BL/6N-Setd6<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631530	M	MP:0002833	increased heart weight	Setd6<tm1.1(KOMP)Mbp>/Setd6<tm1.1(KOMP)Mbp>	C57BL/6N-Setd6<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631530	F	MP:0003131	increased erythrocyte cell number	Setd6<tm1.1(KOMP)Mbp>/Setd6<tm1.1(KOMP)Mbp>	C57BL/6N-Setd6<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631530	F	MP:0002757	decreased vertical activity	Setd6<tm1.1(KOMP)Mbp>/Setd6<tm1.1(KOMP)Mbp>	C57BL/6N-Setd6<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631533	F	MP:0005562	decreased mean corpuscular hemoglobin	Sgms1<tm1a(EUCOMM)Wtsi>/Sgms1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sgms1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631533	M	MP:0000745	tremors	Sgms1<tm1a(EUCOMM)Wtsi>/Sgms1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sgms1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631533	M	MP:0001925	male infertility	Sgms1<tm1a(EUCOMM)Wtsi>/Sgms1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sgms1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631533	F	MP:0010092	increased circulating magnesium level	Sgms1<tm1a(EUCOMM)Wtsi>/Sgms1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sgms1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631533	F	MP:0002968	increased circulating alkaline phosphatase level	Sgms1<tm1a(EUCOMM)Wtsi>/Sgms1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sgms1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631533	M	MP:0003960	increased lean body mass	Sgms1<tm1a(EUCOMM)Wtsi>/Sgms1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sgms1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631533	F	MP:0005553	increased circulating creatinine level	Sgms1<tm1a(EUCOMM)Wtsi>/Sgms1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sgms1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631536	M	MP:0005560	decreased circulating glucose level	Sh3tc2<tm1b(KOMP)Wtsi>/Sh3tc2<tm1b(KOMP)Wtsi>	C57BL/6N-Sh3tc2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631537	M	MP:0005419	decreased circulating serum albumin level	Sik1<tm1.1(KOMP)Vlcg>/Sik1<tm1.1(KOMP)Vlcg>	C57BL/6N-Sik1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631537	M	MP:0002833	increased heart weight	Sik1<tm1.1(KOMP)Vlcg>/Sik1<tm1.1(KOMP)Vlcg>	C57BL/6N-Sik1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631537	M	MP:0010025	decreased total body fat amount	Sik1<tm1.1(KOMP)Vlcg>/Sik1<tm1.1(KOMP)Vlcg>	C57BL/6N-Sik1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631537	M	MP:0003917	increased kidney weight	Sik1<tm1.1(KOMP)Vlcg>/Sik1<tm1.1(KOMP)Vlcg>	C57BL/6N-Sik1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631537	M	MP:0005567	decreased circulating total protein level	Sik1<tm1.1(KOMP)Vlcg>/Sik1<tm1.1(KOMP)Vlcg>	C57BL/6N-Sik1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631537	M	MP:0003960	increased lean body mass	Sik1<tm1.1(KOMP)Vlcg>/Sik1<tm1.1(KOMP)Vlcg>	C57BL/6N-Sik1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631537	M	MP:0005179	decreased circulating cholesterol level	Sik1<tm1.1(KOMP)Vlcg>/Sik1<tm1.1(KOMP)Vlcg>	C57BL/6N-Sik1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631539	F	MP:0005344	increased circulating bilirubin level	Ska2<tm1b(KOMP)Wtsi>/Ska2<+>	C57BL/6N-Ska2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631539	F	MP:0003179	thrombocytopenia	Ska2<tm1b(KOMP)Wtsi>/Ska2<+>	C57BL/6N-Ska2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631539	F	MP:0001556	increased circulating HDL cholesterol level	Ska2<tm1b(KOMP)Wtsi>/Ska2<+>	C57BL/6N-Ska2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631539	F	MP:0002968	increased circulating alkaline phosphatase level	Ska2<tm1b(KOMP)Wtsi>/Ska2<+>	C57BL/6N-Ska2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631539	F	MP:0002941	increased circulating alanine transaminase level	Ska2<tm1b(KOMP)Wtsi>/Ska2<+>	C57BL/6N-Ska2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631539	F	MP:0001399	hyperactivity	Ska2<tm1b(KOMP)Wtsi>/Ska2<+>	C57BL/6N-Ska2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631542	F	MP:0005633	increased circulating sodium level	Slc1a1<tm1b(KOMP)Wtsi>/Slc1a1<tm1b(KOMP)Wtsi>	C57BL/6N-Slc1a1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631542	M	MP:0002574	increased vertical activity	Slc1a1<tm1b(KOMP)Wtsi>/Slc1a1<tm1b(KOMP)Wtsi>	C57BL/6N-Slc1a1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631542	F	MP:0001415	increased exploration in new environment	Slc1a1<tm1b(KOMP)Wtsi>/Slc1a1<tm1b(KOMP)Wtsi>	C57BL/6N-Slc1a1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631542	F	MP:0001307	fused cornea and lens	Slc1a1<tm1b(KOMP)Wtsi>/Slc1a1<tm1b(KOMP)Wtsi>	C57BL/6N-Slc1a1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631542	F	MP:0008810	increased circulating iron level	Slc1a1<tm1b(KOMP)Wtsi>/Slc1a1<tm1b(KOMP)Wtsi>	C57BL/6N-Slc1a1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631543	M	MP:0002574	increased vertical activity	Slc1a3<tm1.1(KOMP)Mbp>/Slc1a3<+>	C57BL/6N-Slc1a3<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5631544	M	MP:0005419	decreased circulating serum albumin level	Slc25a30<tm1a(EUCOMM)Wtsi>/Slc25a30<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc25a30<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631544	F	MP:0004599	abnormal vertebral arch morphology	Slc25a30<tm1a(EUCOMM)Wtsi>/Slc25a30<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc25a30<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631544	M	MP:0010025	decreased total body fat amount	Slc25a30<tm1a(EUCOMM)Wtsi>/Slc25a30<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc25a30<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631544	M	MP:0003960	increased lean body mass	Slc25a30<tm1a(EUCOMM)Wtsi>/Slc25a30<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc25a30<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631544	F	MP:0001289	persistence of hyaloid vascular system	Slc25a30<tm1a(EUCOMM)Wtsi>/Slc25a30<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc25a30<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631551	M	MP:0002941	increased circulating alanine transaminase level	Slc47a2<tm1.1(KOMP)Vlcg>/Slc47a2<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc47a2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631551	F	MP:0000063	decreased bone mineral density	Slc47a2<tm1.1(KOMP)Vlcg>/Slc47a2<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc47a2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631556	M	MP:0030610	absent teeth	Slc6a3<tm1b(KOMP)Wtsi>/Slc6a3<tm1b(KOMP)Wtsi>	C57BL/6N-Slc6a3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631556	M	MP:0002100	abnormal tooth morphology	Slc6a3<tm1b(KOMP)Wtsi>/Slc6a3<tm1b(KOMP)Wtsi>	C57BL/6N-Slc6a3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631569	F	MP:0002075	abnormal coat/hair pigmentation	Snai2<tm1.1(KOMP)Vlcg>/Snai2<tm1.1(KOMP)Vlcg>	C57BL/6N-Snai2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631569	F	MP:0000367	abnormal coat/ hair morphology	Snai2<tm1.1(KOMP)Vlcg>/Snai2<tm1.1(KOMP)Vlcg>	C57BL/6N-Snai2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631577	M	MP:0005633	increased circulating sodium level	Sorbs2<tm1.1(KOMP)Mbp>/Sorbs2<tm1.1(KOMP)Mbp>	C57BL/6N-Sorbs2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631577	M	MP:0005560	decreased circulating glucose level	Sorbs2<tm1.1(KOMP)Mbp>/Sorbs2<tm1.1(KOMP)Mbp>	C57BL/6N-Sorbs2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631577	F	MP:0002968	increased circulating alkaline phosphatase level	Sorbs2<tm1.1(KOMP)Mbp>/Sorbs2<tm1.1(KOMP)Mbp>	C57BL/6N-Sorbs2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631577	M	MP:0010511	shortened PR interval	Sorbs2<tm1.1(KOMP)Mbp>/Sorbs2<tm1.1(KOMP)Mbp>	C57BL/6N-Sorbs2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631577	M	MP:0002702	decreased circulating free fatty acids level	Sorbs2<tm1.1(KOMP)Mbp>/Sorbs2<tm1.1(KOMP)Mbp>	C57BL/6N-Sorbs2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631578	F	MP:0002968	increased circulating alkaline phosphatase level	Sox18<tm1.1(KOMP)Vlcg>/Sox18<tm1.1(KOMP)Vlcg>	C57BL/6N-Sox18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631578	M	MP:0005633	increased circulating sodium level	Sox18<tm1.1(KOMP)Vlcg>/Sox18<tm1.1(KOMP)Vlcg>	C57BL/6N-Sox18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631578	M	MP:0005561	increased mean corpuscular hemoglobin	Sox18<tm1.1(KOMP)Vlcg>/Sox18<tm1.1(KOMP)Vlcg>	C57BL/6N-Sox18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631583	M	MP:0004599	abnormal vertebral arch morphology	Spopl<tm1a(EUCOMM)Wtsi>/Spopl<tm1a(EUCOMM)Wtsi>	C57BL/6N-Spopl<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631584	M	MP:0005560	decreased circulating glucose level	Sptssa<tm1b(KOMP)Wtsi>/Sptssa<+>	C57BL/6N-Sptssa<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631586	M	MP:0013278	decreased fasting circulating glucose level	Sptssb<tm1b(KOMP)Mbp>/Sptssb<tm1b(KOMP)Mbp>	C57BL/6N-Sptssb<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631586	F	MP:0005565	increased blood urea nitrogen level	Sptssb<tm1b(KOMP)Mbp>/Sptssb<tm1b(KOMP)Mbp>	C57BL/6N-Sptssb<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631586	F	MP:0005560	decreased circulating glucose level	Sptssb<tm1b(KOMP)Mbp>/Sptssb<tm1b(KOMP)Mbp>	C57BL/6N-Sptssb<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631586	F	MP:0004151	decreased circulating iron level	Sptssb<tm1b(KOMP)Mbp>/Sptssb<tm1b(KOMP)Mbp>	C57BL/6N-Sptssb<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631586	F	MP:0001510	abnormal coat appearance	Sptssb<tm1b(KOMP)Mbp>/Sptssb<tm1b(KOMP)Mbp>	C57BL/6N-Sptssb<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631586	M	MP:0002833	increased heart weight	Sptssb<tm1b(KOMP)Mbp>/Sptssb<tm1b(KOMP)Mbp>	C57BL/6N-Sptssb<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631593	M	MP:0002574	increased vertical activity	Strn3<tm1b(KOMP)Wtsi>/Strn3<+>	C57BL/6N-Strn3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631593	F	MP:0020870	decreased thigmotaxis	Strn3<tm1b(KOMP)Wtsi>/Strn3<+>	C57BL/6N-Strn3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631593	F	MP:0001399	hyperactivity	Strn3<tm1b(KOMP)Wtsi>/Strn3<+>	C57BL/6N-Strn3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631593	M	MP:0005560	decreased circulating glucose level	Strn3<tm1b(KOMP)Wtsi>/Strn3<+>	C57BL/6N-Strn3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631593	F	MP:0004924	abnormal behavior	Strn3<tm1b(KOMP)Wtsi>/Strn3<+>	C57BL/6N-Strn3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631595	M	MP:0005419	decreased circulating serum albumin level	Stx16<tm1b(KOMP)Wtsi>/Stx16<tm1b(KOMP)Wtsi>	C57BL/6N-Stx16<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631595	F	MP:0013279	increased fasting circulating glucose level	Stx16<tm1b(KOMP)Wtsi>/Stx16<tm1b(KOMP)Wtsi>	C57BL/6N-Stx16<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631595	M	MP:0003960	increased lean body mass	Stx16<tm1b(KOMP)Wtsi>/Stx16<tm1b(KOMP)Wtsi>	C57BL/6N-Stx16<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631595	M	MP:0010123	increased bone mineral content	Stx16<tm1b(KOMP)Wtsi>/Stx16<tm1b(KOMP)Wtsi>	C57BL/6N-Stx16<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631595	F	MP:0001415	increased exploration in new environment	Stx16<tm1b(KOMP)Wtsi>/Stx16<tm1b(KOMP)Wtsi>	C57BL/6N-Stx16<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631595	F	MP:0002941	increased circulating alanine transaminase level	Stx16<tm1b(KOMP)Wtsi>/Stx16<tm1b(KOMP)Wtsi>	C57BL/6N-Stx16<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631595	M	MP:0005292	improved glucose tolerance	Stx16<tm1b(KOMP)Wtsi>/Stx16<tm1b(KOMP)Wtsi>	C57BL/6N-Stx16<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631595	M	MP:0004924	abnormal behavior	Stx16<tm1b(KOMP)Wtsi>/Stx16<tm1b(KOMP)Wtsi>	C57BL/6N-Stx16<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631595	M	MP:0002968	increased circulating alkaline phosphatase level	Stx16<tm1b(KOMP)Wtsi>/Stx16<tm1b(KOMP)Wtsi>	C57BL/6N-Stx16<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631595	M	MP:0020870	decreased thigmotaxis	Stx16<tm1b(KOMP)Wtsi>/Stx16<tm1b(KOMP)Wtsi>	C57BL/6N-Stx16<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631617	M	MP:0005178	increased circulating cholesterol level	Tfec<tm1b(KOMP)Wtsi>/Tfec<tm1b(KOMP)Wtsi>	C57BL/6N-Tfec<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631617	M	MP:0002075	abnormal coat/hair pigmentation	Tfec<tm1b(KOMP)Wtsi>/Tfec<tm1b(KOMP)Wtsi>	C57BL/6N-Tfec<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631622	F	MP:0002590	increased mean corpuscular volume	Timp3<tm1.1(KOMP)Vlcg>/Timp3<tm1.1(KOMP)Vlcg>	C57BL/6N-Timp3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631623	M	MP:0000062	increased bone mineral density	Tm4sf4<tm1.1(KOMP)Vlcg>/Tm4sf4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tm4sf4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631623	F	MP:0001293	anophthalmia	Tm4sf4<tm1.1(KOMP)Vlcg>/Tm4sf4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tm4sf4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631623	F	MP:0001529	abnormal vocalization	Tm4sf4<tm1.1(KOMP)Vlcg>/Tm4sf4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tm4sf4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631624	M	MP:0005632	decreased circulating aspartate transaminase level	Tmc6<tm1a(EUCOMM)Wtsi>/Tmc6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tmc6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5631629	F	MP:0005633	increased circulating sodium level	Tmem151b<tm1b(KOMP)Wtsi>/Tmem151b<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem151b<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631630	M	MP:0000266	abnormal heart morphology	Tmem184b<tm1.1(KOMP)Vlcg>/Tmem184b<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem184b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631630	M	MP:0020870	decreased thigmotaxis	Tmem184b<tm1.1(KOMP)Vlcg>/Tmem184b<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem184b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631630	M	MP:0000274	enlarged heart	Tmem184b<tm1.1(KOMP)Vlcg>/Tmem184b<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem184b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631630	F	MP:0002060	abnormal skin morphology	Tmem184b<tm1.1(KOMP)Vlcg>/Tmem184b<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem184b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631630	M	MP:0004924	abnormal behavior	Tmem184b<tm1.1(KOMP)Vlcg>/Tmem184b<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem184b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631630	M	MP:0002574	increased vertical activity	Tmem184b<tm1.1(KOMP)Vlcg>/Tmem184b<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem184b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631630	M	MP:0001147	small testis	Tmem184b<tm1.1(KOMP)Vlcg>/Tmem184b<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem184b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631630	F	MP:0001258	decreased body length	Tmem184b<tm1.1(KOMP)Vlcg>/Tmem184b<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem184b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631630	M	MP:0002339	abnormal lymph node morphology	Tmem184b<tm1.1(KOMP)Vlcg>/Tmem184b<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem184b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631630	M	MP:0001146	abnormal testis morphology	Tmem184b<tm1.1(KOMP)Vlcg>/Tmem184b<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem184b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631636	F	MP:0011396	abnormal sleep behavior	Tpgs2<tm1.1(KOMP)Vlcg>/Tpgs2<tm1.1(KOMP)Vlcg>	C57BL/6N-Tpgs2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631636	M	MP:0001925	male infertility	Tpgs2<tm1.1(KOMP)Vlcg>/Tpgs2<tm1.1(KOMP)Vlcg>	C57BL/6N-Tpgs2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631636	F	MP:0003131	increased erythrocyte cell number	Tpgs2<tm1.1(KOMP)Vlcg>/Tpgs2<tm1.1(KOMP)Vlcg>	C57BL/6N-Tpgs2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631636	F	MP:0005554	decreased circulating creatinine level	Tpgs2<tm1.1(KOMP)Vlcg>/Tpgs2<tm1.1(KOMP)Vlcg>	C57BL/6N-Tpgs2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631637	F	MP:0009142	decreased prepulse inhibition	Tprn<tm1.1(KOMP)Vlcg>/Tprn<tm1.1(KOMP)Vlcg>	C57BL/6N-Tprn<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631637	F	MP:0001486	abnormal startle reflex	Tprn<tm1.1(KOMP)Vlcg>/Tprn<tm1.1(KOMP)Vlcg>	C57BL/6N-Tprn<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631640	F	MP:0004174	abnormal spine curvature	Tram2<tm1a(KOMP)Wtsi>/Tram2<tm1a(KOMP)Wtsi>	C57BL/6N-Tram2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631640	F	MP:0005419	decreased circulating serum albumin level	Tram2<tm1a(KOMP)Wtsi>/Tram2<tm1a(KOMP)Wtsi>	C57BL/6N-Tram2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631640	F	MP:0000160	kyphosis	Tram2<tm1a(KOMP)Wtsi>/Tram2<tm1a(KOMP)Wtsi>	C57BL/6N-Tram2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631640	M	MP:0005108	abnormal ulna morphology	Tram2<tm1a(KOMP)Wtsi>/Tram2<tm1a(KOMP)Wtsi>	C57BL/6N-Tram2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631640	F	MP:0010052	increased grip strength	Tram2<tm1a(KOMP)Wtsi>/Tram2<tm1a(KOMP)Wtsi>	C57BL/6N-Tram2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631640	F	MP:0002968	increased circulating alkaline phosphatase level	Tram2<tm1a(KOMP)Wtsi>/Tram2<tm1a(KOMP)Wtsi>	C57BL/6N-Tram2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631641	M	MP:0002968	increased circulating alkaline phosphatase level	Trip13<tm1.1(KOMP)Vlcg>/Trip13<+>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631641	M	MP:0001363	increased anxiety-related response	Trip13<tm1.1(KOMP)Vlcg>/Trip13<+>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	F	MP:0003961	decreased lean body mass	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	M	MP:0000218	increased leukocyte cell number	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	F	MP:0000063	decreased bone mineral density	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	M	MP:0000208	decreased hematocrit	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	M	MP:0002875	decreased erythrocyte cell number	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	F	MP:0002797	increased thigmotaxis	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	F	MP:0013279	increased fasting circulating glucose level	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	M	MP:0001925	male infertility	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	M	MP:0002111	abnormal tail morphology	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	F	MP:0001402	decreased locomotor activity	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	F	MP:0010124	decreased bone mineral content	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	F	MP:0002075	abnormal coat/hair pigmentation	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	M	MP:0001556	increased circulating HDL cholesterol level	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	F	MP:0001926	female infertility	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	M	MP:0005561	increased mean corpuscular hemoglobin	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	M	MP:0005178	increased circulating cholesterol level	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	F	MP:0002574	increased vertical activity	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	F	MP:0010053	decreased grip strength	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	F	MP:0001399	hyperactivity	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	F	MP:0005102	abnormal iris pigmentation	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631642	M	MP:0002874	decreased hemoglobin content	Trip13<tm1.1(KOMP)Vlcg>/Trip13<tm1.1(KOMP)Vlcg>	C57BL/6N-Trip13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631644	M	MP:0005560	decreased circulating glucose level	Tspan18<tm1.1(KOMP)Vlcg>/Tspan18<tm1.1(KOMP)Vlcg>	C57BL/6N-Tspan18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631644	M	MP:0005419	decreased circulating serum albumin level	Tspan18<tm1.1(KOMP)Vlcg>/Tspan18<tm1.1(KOMP)Vlcg>	C57BL/6N-Tspan18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631644	M	MP:0002941	increased circulating alanine transaminase level	Tspan18<tm1.1(KOMP)Vlcg>/Tspan18<tm1.1(KOMP)Vlcg>	C57BL/6N-Tspan18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631644	F	MP:0013279	increased fasting circulating glucose level	Tspan18<tm1.1(KOMP)Vlcg>/Tspan18<tm1.1(KOMP)Vlcg>	C57BL/6N-Tspan18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631651	M	MP:0003984	embryonic growth retardation	Ube2c<tm1.1(KOMP)Wtsi>/Ube2c<tm1.1(KOMP)Wtsi>	C57BL/6N-Ube2c<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5631655	M	MP:0011100	preweaning lethality, complete penetrance	Ublcp1<tm1b(KOMP)Wtsi>/Ublcp1<tm1b(KOMP)Wtsi>	C57BL/6N-Ublcp1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5631663	F	MP:0005561	increased mean corpuscular hemoglobin	Usp11<tm1(KOMP)Wtsi>/Usp11<tm1(KOMP)Wtsi>	C57BL/6N-Usp11<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631677	M	MP:0002833	increased heart weight	Vsig8<tm1.1(KOMP)Mbp>/Vsig8<tm1.1(KOMP)Mbp>	C57BL/6N-Vsig8<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631677	M	MP:0005560	decreased circulating glucose level	Vsig8<tm1.1(KOMP)Mbp>/Vsig8<tm1.1(KOMP)Mbp>	C57BL/6N-Vsig8<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631678	M	MP:0001146	abnormal testis morphology	Vti1a<tm1.1(KOMP)Vlcg>/Vti1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Vti1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631678	M	MP:0011110	preweaning lethality, incomplete penetrance	Vti1a<tm1.1(KOMP)Vlcg>/Vti1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Vti1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631678	M	MP:0020870	decreased thigmotaxis	Vti1a<tm1.1(KOMP)Vlcg>/Vti1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Vti1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631678	M	MP:0004931	enlarged epididymis	Vti1a<tm1.1(KOMP)Vlcg>/Vti1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Vti1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631678	M	MP:0004924	abnormal behavior	Vti1a<tm1.1(KOMP)Vlcg>/Vti1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Vti1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631678	F	MP:0013278	decreased fasting circulating glucose level	Vti1a<tm1.1(KOMP)Vlcg>/Vti1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Vti1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631678	M	MP:0002968	increased circulating alkaline phosphatase level	Vti1a<tm1.1(KOMP)Vlcg>/Vti1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Vti1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631678	M	MP:0002631	abnormal epididymis morphology	Vti1a<tm1.1(KOMP)Vlcg>/Vti1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Vti1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631678	M	MP:0001513	limb grasping	Vti1a<tm1.1(KOMP)Vlcg>/Vti1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Vti1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631678	M	MP:0001258	decreased body length	Vti1a<tm1.1(KOMP)Vlcg>/Vti1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Vti1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631678	M	MP:0001399	hyperactivity	Vti1a<tm1.1(KOMP)Vlcg>/Vti1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Vti1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631687	M	MP:0001258	decreased body length	Wnt10a<tm1.1(KOMP)Vlcg>/Wnt10a<tm1.1(KOMP)Vlcg>	C57BL/6N-Wnt10a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631687	M	MP:0010025	decreased total body fat amount	Wnt10a<tm1.1(KOMP)Vlcg>/Wnt10a<tm1.1(KOMP)Vlcg>	C57BL/6N-Wnt10a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631687	F	MP:0002075	abnormal coat/hair pigmentation	Wnt10a<tm1.1(KOMP)Vlcg>/Wnt10a<tm1.1(KOMP)Vlcg>	C57BL/6N-Wnt10a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631687	F	MP:0002764	short tibia	Wnt10a<tm1.1(KOMP)Vlcg>/Wnt10a<tm1.1(KOMP)Vlcg>	C57BL/6N-Wnt10a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631693	M	MP:0000438	abnormal cranium morphology	Xpnpep1<tm1a(KOMP)Wtsi>/Xpnpep1<tm1a(KOMP)Wtsi>	C57BL/6N-Xpnpep1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631693	M	MP:0008346	increased gamma-delta T cell number	Xpnpep1<tm1a(KOMP)Wtsi>/Xpnpep1<tm1a(KOMP)Wtsi>	C57BL/6N-Xpnpep1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631696	M	MP:0010025	decreased total body fat amount	Ydjc<tm1(KOMP)Wtsi>/Ydjc<tm1(KOMP)Wtsi>	C57BL/6N-Ydjc<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631696	F	MP:0001325	abnormal retina morphology	Ydjc<tm1(KOMP)Wtsi>/Ydjc<tm1(KOMP)Wtsi>	C57BL/6N-Ydjc<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631696	M	MP:0003960	increased lean body mass	Ydjc<tm1(KOMP)Wtsi>/Ydjc<tm1(KOMP)Wtsi>	C57BL/6N-Ydjc<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5631699	F	MP:0001258	decreased body length	Ypel3<tm1.1(KOMP)Vlcg>/Ypel3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ypel3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631699	M	MP:0002574	increased vertical activity	Ypel3<tm1.1(KOMP)Vlcg>/Ypel3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ypel3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631699	F	MP:0002968	increased circulating alkaline phosphatase level	Ypel3<tm1.1(KOMP)Vlcg>/Ypel3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ypel3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631699	M	MP:0006203	eye hemorrhage	Ypel3<tm1.1(KOMP)Vlcg>/Ypel3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ypel3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631699	M	MP:0002590	increased mean corpuscular volume	Ypel3<tm1.1(KOMP)Vlcg>/Ypel3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ypel3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631699	F	MP:0001486	abnormal startle reflex	Ypel3<tm1.1(KOMP)Vlcg>/Ypel3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ypel3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631699	M	MP:0002764	short tibia	Ypel3<tm1.1(KOMP)Vlcg>/Ypel3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ypel3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631699	F	MP:0001399	hyperactivity	Ypel3<tm1.1(KOMP)Vlcg>/Ypel3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ypel3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631700	M	MP:0005633	increased circulating sodium level	Zbtb32<tm1b(KOMP)Mbp>/Zbtb32<tm1b(KOMP)Mbp>	C57BL/6N-Zbtb32<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631700	M	MP:0002702	decreased circulating free fatty acids level	Zbtb32<tm1b(KOMP)Mbp>/Zbtb32<tm1b(KOMP)Mbp>	C57BL/6N-Zbtb32<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631700	M	MP:0020870	decreased thigmotaxis	Zbtb32<tm1b(KOMP)Mbp>/Zbtb32<tm1b(KOMP)Mbp>	C57BL/6N-Zbtb32<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631700	M	MP:0002079	increased circulating insulin level	Zbtb32<tm1b(KOMP)Mbp>/Zbtb32<tm1b(KOMP)Mbp>	C57BL/6N-Zbtb32<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631700	M	MP:0004924	abnormal behavior	Zbtb32<tm1b(KOMP)Mbp>/Zbtb32<tm1b(KOMP)Mbp>	C57BL/6N-Zbtb32<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631706	F	MP:0001554	increased circulating free fatty acids level	Zfp346<tm1.1(KOMP)Vlcg>/Zfp346<+>	C57BL/6N-Zfp346<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5631708	M	MP:0005419	decreased circulating serum albumin level	Zfp42<tm1b(KOMP)Mbp>/Zfp42<+>	C57BL/6N-Zfp42<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631708	M	MP:0020870	decreased thigmotaxis	Zfp42<tm1b(KOMP)Mbp>/Zfp42<+>	C57BL/6N-Zfp42<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5631709	M	MP:0003019	increased circulating chloride level	Zfp536<tm1.1(KOMP)Wtsi>/Zfp536<+>	C57BL/6N-Zfp536<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631709	M	MP:0005564	increased hemoglobin content	Zfp536<tm1.1(KOMP)Wtsi>/Zfp536<+>	C57BL/6N-Zfp536<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5631711	F	MP:0020870	decreased thigmotaxis	Zhx3<tm1.1(KOMP)Vlcg>/Zhx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Zhx3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631711	M	MP:0010025	decreased total body fat amount	Zhx3<tm1.1(KOMP)Vlcg>/Zhx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Zhx3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631711	M	MP:0001415	increased exploration in new environment	Zhx3<tm1.1(KOMP)Vlcg>/Zhx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Zhx3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631711	F	MP:0005343	increased circulating aspartate transaminase level	Zhx3<tm1.1(KOMP)Vlcg>/Zhx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Zhx3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631711	F	MP:0004924	abnormal behavior	Zhx3<tm1.1(KOMP)Vlcg>/Zhx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Zhx3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631711	F	MP:0001399	hyperactivity	Zhx3<tm1.1(KOMP)Vlcg>/Zhx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Zhx3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631711	F	MP:0001257	increased body length	Zhx3<tm1.1(KOMP)Vlcg>/Zhx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Zhx3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631711	F	MP:0000062	increased bone mineral density	Zhx3<tm1.1(KOMP)Vlcg>/Zhx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Zhx3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5631711	M	MP:0003960	increased lean body mass	Zhx3<tm1.1(KOMP)Vlcg>/Zhx3<tm1.1(KOMP)Vlcg>	C57BL/6N-Zhx3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5632295	M	MP:0001925	male infertility	Grid2<ho>/Grid2<ho>	involves: C57BLKS/J	N	MGI:61633
MGI:5633962	M	MP:0000659	prostate gland hyperplasia	Tg(H-2K1-Lrp5/Fkbp1a,-luc*)#Dmps/0	involves: FVB/N	N	22303459
MGI:5633962	M	MP:0000659	prostate gland hyperplasia	Tg(H-2K1-Lrp5/Fkbp1a,-luc*)#Dmps/0	involves: FVB/N	N	24305876
MGI:5633962	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(H-2K1-Lrp5/Fkbp1a,-luc*)#Dmps/0	involves: FVB/N	N	22303459
MGI:5633962	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(H-2K1-Lrp5/Fkbp1a,-luc*)#Dmps/0	involves: FVB/N	N	24305876
MGI:5633986	M	MP:0000659	prostate gland hyperplasia	Tg(Pbsn-Lrp5/Fkbp1a,-luc*)#Dmps/0	involves: FVB/N	N	24305876
MGI:5633987	M	MP:0010367	increased spindle cell carcinoma incidence	Tg(H-2K1-Lrp5/Fkbp1a,-luc*)#Dmps/0,Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0	involves: FVB/N	N	24305876
MGI:5633987	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(H-2K1-Lrp5/Fkbp1a,-luc*)#Dmps/0,Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0	involves: FVB/N	N	24305876
MGI:5633988	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0,Tg(Pbsn-Lrp5/Fkbp1a,-luc*)#Dmps/0	involves: FVB/N	N	24305876
MGI:5634270	M	MP:0012035	abnormal b-wave shape	Cacna1f<tm1.1Sdie>/Y	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634270	M	MP:0008518	retina outer nuclear layer degeneration	Cacna1f<tm1.1Sdie>/Y	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634270	M	MP:0009538	abnormal synapse morphology	Cacna1f<tm1.1Sdie>/Y	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634270	M	MP:0006072	abnormal retina apoptosis	Cacna1f<tm1.1Sdie>/Y	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634270	M	MP:0012034	abnormal a-wave shape	Cacna1f<tm1.1Sdie>/Y	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634270	M	MP:0005253	abnormal eye physiology	Cacna1f<tm1.1Sdie>/Y	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634270	M	MP:0008515	thin retina outer nuclear layer	Cacna1f<tm1.1Sdie>/Y	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634270	M	MP:0004811	abnormal neuron physiology	Cacna1f<tm1.1Sdie>/Y	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634270	M	MP:0008450	retina photoreceptor degeneration	Cacna1f<tm1.1Sdie>/Y	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634270	M	MP:0012143	decreased a-wave amplitude	Cacna1f<tm1.1Sdie>/Y	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634270	M	MP:0012029	abnormal electroretinogram waveform feature	Cacna1f<tm1.1Sdie>/Y	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634271	F	MP:0008450	retina photoreceptor degeneration	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634271	F	MP:0008518	retina outer nuclear layer degeneration	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634271	F	MP:0004811	abnormal neuron physiology	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634271	F	MP:0005253	abnormal eye physiology	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634271	F	MP:0012143	decreased a-wave amplitude	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634271	F	MP:0012034	abnormal a-wave shape	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634271	F	MP:0008515	thin retina outer nuclear layer	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634271	F	MP:0006072	abnormal retina apoptosis	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634271	F	MP:0009538	abnormal synapse morphology	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634271	F	MP:0012029	abnormal electroretinogram waveform feature	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634271	F	MP:0012035	abnormal b-wave shape	Cacna1f<tm1.1Sdie>/Cacna1f<tm1.1Sdie>	B6.Cg-Cacna1f<tm1.1Sdie>/J	N	24466230
MGI:5634274	F	MP:0004811	abnormal neuron physiology	Cacna1f<tm1.2Sdie>/Cacna1f<tm1.2Sdie>	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634274	F	MP:0008450	retina photoreceptor degeneration	Cacna1f<tm1.2Sdie>/Cacna1f<tm1.2Sdie>	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634274	F	MP:0008515	thin retina outer nuclear layer	Cacna1f<tm1.2Sdie>/Cacna1f<tm1.2Sdie>	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634274	F	MP:0005253	abnormal eye physiology	Cacna1f<tm1.2Sdie>/Cacna1f<tm1.2Sdie>	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634274	F	MP:0009538	abnormal synapse morphology	Cacna1f<tm1.2Sdie>/Cacna1f<tm1.2Sdie>	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634274	F	MP:0008451	retina rod cell degeneration	Cacna1f<tm1.2Sdie>/Cacna1f<tm1.2Sdie>	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634274	F	MP:0030005	increased retina apoptosis	Cacna1f<tm1.2Sdie>/Cacna1f<tm1.2Sdie>	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634274	F	MP:0012029	abnormal electroretinogram waveform feature	Cacna1f<tm1.2Sdie>/Cacna1f<tm1.2Sdie>	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634274	F	MP:0012144	decreased b-wave amplitude	Cacna1f<tm1.2Sdie>/Cacna1f<tm1.2Sdie>	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634274	F	MP:0012143	decreased a-wave amplitude	Cacna1f<tm1.2Sdie>/Cacna1f<tm1.2Sdie>	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634279	M	MP:0008515	thin retina outer nuclear layer	Cacna1f<tm1.2Sdie>/Y	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634279	M	MP:0012029	abnormal electroretinogram waveform feature	Cacna1f<tm1.2Sdie>/Y	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634279	M	MP:0008450	retina photoreceptor degeneration	Cacna1f<tm1.2Sdie>/Y	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634279	M	MP:0005253	abnormal eye physiology	Cacna1f<tm1.2Sdie>/Y	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634279	M	MP:0009538	abnormal synapse morphology	Cacna1f<tm1.2Sdie>/Y	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634279	M	MP:0012143	decreased a-wave amplitude	Cacna1f<tm1.2Sdie>/Y	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634279	M	MP:0008451	retina rod cell degeneration	Cacna1f<tm1.2Sdie>/Y	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634279	M	MP:0004811	abnormal neuron physiology	Cacna1f<tm1.2Sdie>/Y	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634279	M	MP:0030005	increased retina apoptosis	Cacna1f<tm1.2Sdie>/Y	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634279	M	MP:0012144	decreased b-wave amplitude	Cacna1f<tm1.2Sdie>/Y	B6.Cg-Cacna1f<tm1.2Sdie>/J	N	24466230
MGI:5634972	F	MP:0005643	decreased dopamine level	Per1<tm1Drw>/Per1<tm1Drw>	B6.129-Per1<tm1Drw>/J	N	25673850
MGI:5635158	M	MP:0003205	testicular atrophy	Tg(HTT*)NXwy/0	involves: FVB/NJ	N	25661181
MGI:5635158	M	MP:0001925	male infertility	Tg(HTT*)NXwy/0	involves: FVB/NJ	N	25661181
MGI:5636613	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm2Mak>/Pten<tm2Mak>,Tg(KLK3-cre)13Saa/0	involves: 129P2/OlaHsd * C57BL/6	N	24986896
MGI:5636613	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm2Mak>/Pten<tm2Mak>,Tg(KLK3-cre)13Saa/0	involves: 129P2/OlaHsd * C57BL/6	N	24986896
MGI:5636613	M	MP:0002083	premature death	Pten<tm2Mak>/Pten<tm2Mak>,Tg(KLK3-cre)13Saa/0	involves: 129P2/OlaHsd * C57BL/6	N	24986896
MGI:5636613	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm2Mak>/Pten<tm2Mak>,Tg(KLK3-cre)13Saa/0	involves: 129P2/OlaHsd * C57BL/6	N	24986896
MGI:5636613	M	MP:0001272	increased metastatic potential	Pten<tm2Mak>/Pten<tm2Mak>,Tg(KLK3-cre)13Saa/0	involves: 129P2/OlaHsd * C57BL/6	N	24986896
MGI:5637537	M	MP:0011613	decreased circulating ghrelin level	Trhr<tm1Bau>/Trhr<tm1Bau>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25490146
MGI:5637537	M	MP:0001262	decreased body weight	Trhr<tm1Bau>/Trhr<tm1Bau>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25490146
MGI:5637537	M	MP:0003351	decreased circulating levels of thyroid hormone	Trhr<tm1Bau>/Trhr<tm1Bau>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25490146
MGI:5637537	M	MP:0005479	decreased circulating triiodothyronine level	Trhr<tm1Bau>/Trhr<tm1Bau>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25490146
MGI:5637537	M	MP:0005289	increased oxygen consumption	Trhr<tm1Bau>/Trhr<tm1Bau>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25490146
MGI:5637537	M	MP:0011612	increased circulating ghrelin level	Trhr<tm1Bau>/Trhr<tm1Bau>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25490146
MGI:5637537	M	MP:0003503	decreased activity of thyroid gland	Trhr<tm1Bau>/Trhr<tm1Bau>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25490146
MGI:5637537	M	MP:0001263	weight loss	Trhr<tm1Bau>/Trhr<tm1Bau>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25490146
MGI:5637537	M	MP:0005478	decreased circulating thyroxine level	Trhr<tm1Bau>/Trhr<tm1Bau>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25490146
MGI:5637537	M	MP:0011611	abnormal circulating ghrelin level	Trhr<tm1Bau>/Trhr<tm1Bau>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25490146
MGI:5637726	F	MP:0003243	abnormal dopaminergic neuron morphology	Hprt1<b-m3>/Hprt1<b-m3>	B6.129P2-Hprt1<b-m3>	N	7509865
MGI:5637726	F	MP:0012592	decreased brain choline acetyltransferase activity	Hprt1<b-m3>/Hprt1<b-m3>	B6.129P2-Hprt1<b-m3>	N	7509865
MGI:5637726	F	MP:0020078	decreased brain tyrosine 3-monooxygenase activity	Hprt1<b-m3>/Hprt1<b-m3>	B6.129P2-Hprt1<b-m3>	N	7509865
MGI:5637726	F	MP:0005643	decreased dopamine level	Hprt1<b-m3>/Hprt1<b-m3>	B6.129P2-Hprt1<b-m3>	N	7509865
MGI:5637742	F	MP:0004024	aneuploidy	Tg(MMTV-Espl1)1Pati/0	involves: C57BL/6	N	24276237
MGI:5637742	F	MP:0006271	abnormal involution of the mammary gland	Tg(MMTV-Espl1)1Pati/0	involves: C57BL/6	N	24276237
MGI:5637742	F	MP:0003702	abnormal chromosome morphology	Tg(MMTV-Espl1)1Pati/0	involves: C57BL/6	N	24276237
MGI:5637742	F	MP:0008866	chromosomal instability	Tg(MMTV-Espl1)1Pati/0	involves: C57BL/6	N	24276237
MGI:5637742	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-Espl1)1Pati/0	involves: C57BL/6	N	24276237
MGI:5637742	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-Espl1)1Pati/0	involves: C57BL/6	N	24276237
MGI:5637742	F	MP:0000630	mammary gland hyperplasia	Tg(MMTV-Espl1)1Pati/0	involves: C57BL/6	N	24276237
MGI:5637814	M	MP:0002981	increased liver weight	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	17029217
MGI:5637814	M	MP:0014045	Mallory bodies	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	17029217
MGI:5637814	M	MP:0003333	liver fibrosis	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	18637146
MGI:5637814	M	MP:0003331	increased hepatocellular carcinoma incidence	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	18637146
MGI:5637814	M	MP:0000607	abnormal hepatocyte morphology	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	17029217
MGI:5637814	M	MP:0001656	focal hepatic necrosis	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	17029217
MGI:5637814	M	MP:0003674	oxidative stress	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	17029217
MGI:5637814	M	MP:0001656	focal hepatic necrosis	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	18637146
MGI:5637814	M	MP:0009355	increased liver triglyceride level	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	17029217
MGI:5637814	M	MP:0001860	liver inflammation	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	18637146
MGI:5637814	M	MP:0000598	abnormal liver morphology	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	18637146
MGI:5637814	M	MP:0002628	hepatic steatosis	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	17029217
MGI:5637814	M	MP:0000598	abnormal liver morphology	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	17029217
MGI:5637814	M	MP:0002941	increased circulating alanine transaminase level	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	17029217
MGI:5637814	M	MP:0002628	hepatic steatosis	Lgals3<tm1Ftl>/Lgals3<tm1Ftl>	involves: 129S2/SvPas * CD-1	N	18637146
MGI:5638149	M	MP:0005217	abnormal pancreatic beta cell morphology	Foxm1<tm1Rhc>/Foxm1<tm1Rhc>,Tg(Pdx1-cre)89.1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	16556734
MGI:5638149	M	MP:0009109	decreased pancreas weight	Foxm1<tm1Rhc>/Foxm1<tm1Rhc>,Tg(Pdx1-cre)89.1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	16556734
MGI:5638149	M	MP:0011820	decreased pancreatic beta cell proliferation	Foxm1<tm1Rhc>/Foxm1<tm1Rhc>,Tg(Pdx1-cre)89.1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	16556734
MGI:5638149	M	MP:0005215	abnormal pancreatic islet morphology	Foxm1<tm1Rhc>/Foxm1<tm1Rhc>,Tg(Pdx1-cre)89.1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	16556734
MGI:5638149	M	MP:0009176	increased pancreatic alpha cell number	Foxm1<tm1Rhc>/Foxm1<tm1Rhc>,Tg(Pdx1-cre)89.1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	16556734
MGI:5638149	M	MP:0005293	impaired glucose tolerance	Foxm1<tm1Rhc>/Foxm1<tm1Rhc>,Tg(Pdx1-cre)89.1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	16556734
MGI:5638149	M	MP:0003336	pancreas cyst	Foxm1<tm1Rhc>/Foxm1<tm1Rhc>,Tg(Pdx1-cre)89.1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	16556734
MGI:5638149	M	MP:0003564	abnormal insulin secretion	Foxm1<tm1Rhc>/Foxm1<tm1Rhc>,Tg(Pdx1-cre)89.1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	16556734
MGI:5638149	M	MP:0003339	decreased pancreatic beta cell number	Foxm1<tm1Rhc>/Foxm1<tm1Rhc>,Tg(Pdx1-cre)89.1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	16556734
MGI:5638149	M	MP:0005220	abnormal exocrine pancreas morphology	Foxm1<tm1Rhc>/Foxm1<tm1Rhc>,Tg(Pdx1-cre)89.1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	16556734
MGI:5638149	M	MP:0009148	pancreas necrosis	Foxm1<tm1Rhc>/Foxm1<tm1Rhc>,Tg(Pdx1-cre)89.1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	16556734
MGI:5638149	M	MP:0002078	abnormal glucose homeostasis	Foxm1<tm1Rhc>/Foxm1<tm1Rhc>,Tg(Pdx1-cre)89.1Dam/0	involves: 129X1/SvJ * C57BL/6 * CBA	N	16556734
MGI:5638543	M	MP:0001925	male infertility	Del(7)Tyr<c-3H>/Del(7)Tyr<c-6H>	involves: 101/H * C3H/HeH	N	690964
MGI:5638543	M	MP:0006362	abnormal male germ cell morphology	Del(7)Tyr<c-3H>/Del(7)Tyr<c-6H>	involves: 101/H * C3H/HeH	N	690964
MGI:5638543	F	MP:0003718	maternal effect	Del(7)Tyr<c-3H>/Del(7)Tyr<c-6H>	involves: 101/H * C3H/HeH	N	690964
MGI:5638543	M	MP:0009232	abnormal sperm nucleus morphology	Del(7)Tyr<c-3H>/Del(7)Tyr<c-6H>	involves: 101/H * C3H/HeH	N	690964
MGI:5638543	F	MP:0001926	female infertility	Del(7)Tyr<c-3H>/Del(7)Tyr<c-6H>	involves: 101/H * C3H/HeH	N	690964
MGI:5638543	M	MP:0001929	abnormal gametogenesis	Del(7)Tyr<c-3H>/Del(7)Tyr<c-6H>	involves: 101/H * C3H/HeH	N	690964
MGI:5638543	M	MP:0001932	abnormal spermiogenesis	Del(7)Tyr<c-3H>/Del(7)Tyr<c-6H>	involves: 101/H * C3H/HeH	N	690964
MGI:5639272	M	MP:0003484	abnormal channel response	Tg(Prnp-SNCA*A53T)AAub/?	involves: FVB/N	N	25297088
MGI:5639272	M	MP:0002272	abnormal nervous system electrophysiology	Tg(Prnp-SNCA*A53T)AAub/?	involves: FVB/N	N	25297088
MGI:5639272	M	MP:0004811	abnormal neuron physiology	Tg(Prnp-SNCA*A53T)AAub/?	involves: FVB/N	N	25297088
MGI:5639392	M	MP:0001147	small testis	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<tm1.1(KOMP)Vlcg>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5639392	M	MP:0002060	abnormal skin morphology	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<tm1.1(KOMP)Vlcg>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5639392	M	MP:0003917	increased kidney weight	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<tm1.1(KOMP)Vlcg>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5639392	M	MP:0004952	increased spleen weight	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<tm1.1(KOMP)Vlcg>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5639392	M	MP:0001146	abnormal testis morphology	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<tm1.1(KOMP)Vlcg>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5639396	M	MP:0002591	decreased mean corpuscular volume	Mdk<tm1.1(KOMP)Mbp>/Mdk<tm1.1(KOMP)Mbp>	C57BL/6N-Mdk<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5639396	M	MP:0001556	increased circulating HDL cholesterol level	Mdk<tm1.1(KOMP)Mbp>/Mdk<tm1.1(KOMP)Mbp>	C57BL/6N-Mdk<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5639396	M	MP:0005178	increased circulating cholesterol level	Mdk<tm1.1(KOMP)Mbp>/Mdk<tm1.1(KOMP)Mbp>	C57BL/6N-Mdk<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5639403	F	MP:0010053	decreased grip strength	Prom2<tm1.1(KOMP)Vlcg>/Prom2<+>	C57BL/6N-Prom2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5639403	F	MP:0001399	hyperactivity	Prom2<tm1.1(KOMP)Vlcg>/Prom2<+>	C57BL/6N-Prom2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5639403	F	MP:0005343	increased circulating aspartate transaminase level	Prom2<tm1.1(KOMP)Vlcg>/Prom2<+>	C57BL/6N-Prom2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5639403	F	MP:0000195	decreased circulating calcium level	Prom2<tm1.1(KOMP)Vlcg>/Prom2<+>	C57BL/6N-Prom2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5639403	F	MP:0004151	decreased circulating iron level	Prom2<tm1.1(KOMP)Vlcg>/Prom2<+>	C57BL/6N-Prom2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5639403	F	MP:0005627	increased circulating potassium level	Prom2<tm1.1(KOMP)Vlcg>/Prom2<+>	C57BL/6N-Prom2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5639404	F	MP:0002699	abnormal vitreous body morphology	Satb1<tm1b(EUCOMM)Hmgu>/Satb1<+>	C57BL/6N-Satb1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5639408	M	MP:0001399	hyperactivity	Snph<tm1.1(KOMP)Vlcg>/Snph<tm1.1(KOMP)Vlcg>	C57BL/6N-Snph<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5639408	F	MP:0001258	decreased body length	Snph<tm1.1(KOMP)Vlcg>/Snph<tm1.1(KOMP)Vlcg>	C57BL/6N-Snph<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5639408	F	MP:0010124	decreased bone mineral content	Snph<tm1.1(KOMP)Vlcg>/Snph<tm1.1(KOMP)Vlcg>	C57BL/6N-Snph<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5639408	M	MP:0002175	decreased brain weight	Snph<tm1.1(KOMP)Vlcg>/Snph<tm1.1(KOMP)Vlcg>	C57BL/6N-Snph<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5640613	M	MP:0001399	hyperactivity	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>	N	28218824
MGI:5640613	M	MP:0001402	decreased locomotor activity	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>	N	28218824
MGI:5640613	M	MP:0020467	abnormal circadian behavior	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>	N	28218824
MGI:5640613	M	MP:0004851	increased testis weight	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>	N	21215802
MGI:5640613	M	MP:0004851	increased testis weight	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>	N	11008180
MGI:5640613	M	MP:0011737	hypodipsia	Fmr1<tm1Cgr>/Y	B6.129P2-Fmr1<tm1Cgr>	N	28218824
MGI:5641392	M	MP:0001364	decreased anxiety-related response	Tsc1<tm1Hin>/Tsc1<+>	B6J.129S4-Tsc1<tm1Hin>	N	23250422
MGI:5641392	M	MP:0005498	hyporesponsive to tactile stimuli	Tsc1<tm1Hin>/Tsc1<+>	B6J.129S4-Tsc1<tm1Hin>	N	23250422
MGI:5641482	M	MP:0002566	abnormal sexual interaction	Tsc1<tm1Djk>/Tsc1<+>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22763451
MGI:5641482	M	MP:0001441	increased grooming behavior	Tsc1<tm1Djk>/Tsc1<+>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22763451
MGI:5641482	M	MP:0001360	abnormal social investigation	Tsc1<tm1Djk>/Tsc1<+>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22763451
MGI:5641482	M	MP:0003462	abnormal response to novel odor	Tsc1<tm1Djk>/Tsc1<+>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22763451
MGI:5641483	M	MP:0001405	impaired coordination	Tsc1<tm1Djk>/Tsc1<tm1Djk>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22763451
MGI:5641483	M	MP:0002566	abnormal sexual interaction	Tsc1<tm1Djk>/Tsc1<tm1Djk>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22763451
MGI:5641483	M	MP:0001393	ataxia	Tsc1<tm1Djk>/Tsc1<tm1Djk>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22763451
MGI:5641483	M	MP:0001441	increased grooming behavior	Tsc1<tm1Djk>/Tsc1<tm1Djk>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22763451
MGI:5641483	M	MP:0001360	abnormal social investigation	Tsc1<tm1Djk>/Tsc1<tm1Djk>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22763451
MGI:5641483	M	MP:0002063	abnormal learning/memory/conditioning	Tsc1<tm1Djk>/Tsc1<tm1Djk>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22763451
MGI:5641483	M	MP:0003462	abnormal response to novel odor	Tsc1<tm1Djk>/Tsc1<tm1Djk>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22763451
MGI:5641483	M	MP:0001407	short stride length	Tsc1<tm1Djk>/Tsc1<tm1Djk>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J	N	22763451
MGI:5641710	F	MP:0004906	enlarged uterus	Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23820898
MGI:5641710	F	MP:0013401	increased endometrial gland number	Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23820898
MGI:5641710	F	MP:0008014	increased lung tumor incidence	Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23820898
MGI:5641710	F	MP:0008256	abnormal myometrium morphology	Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23820898
MGI:5641710	F	MP:0001272	increased metastatic potential	Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23820898
MGI:5641710	F	MP:0009092	endometrium hyperplasia	Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23820898
MGI:5641710	F	MP:0001634	internal hemorrhage	Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23820898
MGI:5641710	F	MP:0003570	increased uterus leiomyoma incidence	Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23820898
MGI:5641710	F	MP:0004904	increased uterus weight	Tsc2<tm1.1Mjg>/Tsc2<tm1.1Mjg>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23820898
MGI:5642117	F	MP:0001926	female infertility	Fgfr1<tm1Upir>/Fgfr1<tm1Upir>,Fgfr2<tm1Dor>/Fgfr2<tm1Dor>,Tg(KRT5-cre)5132Jlj/0	involves: 129X1/SvJ * C57BL/6 * C57BL/6J * DBA/2J	N	20308431
MGI:5642117	M	MP:0001922	reduced male fertility	Fgfr1<tm1Upir>/Fgfr1<tm1Upir>,Fgfr2<tm1Dor>/Fgfr2<tm1Dor>,Tg(KRT5-cre)5132Jlj/0	involves: 129X1/SvJ * C57BL/6 * C57BL/6J * DBA/2J	N	20308431
MGI:5642134	M	MP:0001922	reduced male fertility	Cpa3<tm3(icre)Hrr>/Cpa3<+>,Fgfr1<tm1Upir>/Fgfr1<tm1Upir>,Fgfr2<tm1Dor>/Fgfr2<tm1Dor>,Tg(KRT5-cre)5132Jlj/0	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * C57BL/6J * DBA/2J	N	25843682
MGI:5642134	F	MP:0001926	female infertility	Cpa3<tm3(icre)Hrr>/Cpa3<+>,Fgfr1<tm1Upir>/Fgfr1<tm1Upir>,Fgfr2<tm1Dor>/Fgfr2<tm1Dor>,Tg(KRT5-cre)5132Jlj/0	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * C57BL/6J * DBA/2J	N	25843682
MGI:5642428	F	MP:0010053	decreased grip strength	Crym<tm1b(KOMP)Wtsi>/Crym<tm1b(KOMP)Wtsi>	B6N(Cg)-Crym<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5642432	F	MP:0011396	abnormal sleep behavior	Dnajb12<tm1.1(KOMP)Vlcg>/Dnajb12<+>	C57BL/6N-Dnajb12<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5642432	M	MP:0000955	abnormal spinal cord morphology	Dnajb12<tm1.1(KOMP)Vlcg>/Dnajb12<+>	C57BL/6N-Dnajb12<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5642442	M	MP:0001325	abnormal retina morphology	Kcnh3<tm1.1(KOMP)Vlcg>/Kcnh3<+>	C57BL/6N-Kcnh3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5642442	M	MP:0001554	increased circulating free fatty acids level	Kcnh3<tm1.1(KOMP)Vlcg>/Kcnh3<+>	C57BL/6N-Kcnh3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5642447	M	MP:0002833	increased heart weight	Nes<tm1b(KOMP)Wtsi>/Nes<tm1b(KOMP)Wtsi>	C57BL/6N-Nes<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5643859	M	MP:0001263	weight loss	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	21031341
MGI:5643859	M	MP:0006378	abnormal spermatogonia morphology	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	19664290
MGI:5643859	M	MP:0009230	abnormal sperm head morphology	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	19664290
MGI:5643859	M	MP:0005250	decreased Sertoli cell number	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	19664290
MGI:5643859	F	MP:0005289	increased oxygen consumption	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	24710642
MGI:5643859	F	MP:0005560	decreased circulating glucose level	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	21031341
MGI:5643859	M	MP:0005376	homeostasis/metabolism phenotype	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	Y	19664290
MGI:5643859	M	MP:0031436	decreased copulatory plug deposition	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	19664290
MGI:5643859	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	19664290
MGI:5643859	M	MP:0001922	reduced male fertility	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	19664290
MGI:5643859	M	MP:0031426	increased sperm motility	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	19664290
MGI:5643859	M	MP:0009642	abnormal blood homeostasis	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	21031341
MGI:5643859	M	MP:0008892	abnormal sperm flagellum morphology	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	19664290
MGI:5643859	M	MP:0004901	decreased male germ cell number	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	19664290
MGI:5643859	M	MP:0001559	hyperglycemia	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	21031341
MGI:5643859	M	MP:0005668	decreased circulating leptin level	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	24710642
MGI:5643859	M	MP:0002727	decreased circulating insulin level	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	21031341
MGI:5643859	M	MP:0002216	abnormal seminiferous tubule morphology	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	19664290
MGI:5643859	F	MP:0002574	increased vertical activity	Wfs1<tm1Koks>/Wfs1<tm1Koks>	129S6/SvEvTac-Wfs1<tm1Koks>	N	24710642
MGI:5643944	M	MP:0010149	abnormal synaptic dopamine release	Slc6a3<tm1Rbl>/Slc6a3<tm1Rbl>	involves: 129S6/SvEvTac * C57BL/6J	N	25331903
MGI:5643944	M	MP:0004924	abnormal behavior	Slc6a3<tm1Rbl>/Slc6a3<tm1Rbl>	involves: 129S6/SvEvTac * C57BL/6J	N	24332984
MGI:5643944	M	MP:0001906	increased dopamine level	Slc6a3<tm1Rbl>/Slc6a3<tm1Rbl>	involves: 129S6/SvEvTac * C57BL/6J	N	25331903
MGI:5643944	M	MP:0009745	abnormal behavioral response to xenobiotic	Slc6a3<tm1Rbl>/Slc6a3<tm1Rbl>	involves: 129S6/SvEvTac * C57BL/6J	N	25331903
MGI:5643944	M	MP:0002945	abnormal inhibitory postsynaptic currents	Slc6a3<tm1Rbl>/Slc6a3<tm1Rbl>	involves: 129S6/SvEvTac * C57BL/6J	N	25331903
MGI:5643944	M	MP:0004924	abnormal behavior	Slc6a3<tm1Rbl>/Slc6a3<tm1Rbl>	involves: 129S6/SvEvTac * C57BL/6J	N	25331903
MGI:5643944	M	MP:0010069	increased serotonin level	Slc6a3<tm1Rbl>/Slc6a3<tm1Rbl>	involves: 129S6/SvEvTac * C57BL/6J	N	25331903
MGI:5643944	M	MP:0008874	decreased physiological sensitivity to xenobiotic	Slc6a3<tm1Rbl>/Slc6a3<tm1Rbl>	involves: 129S6/SvEvTac * C57BL/6J	N	25331903
MGI:5643944	M	MP:0010831	lethality, incomplete penetrance	Slc6a3<tm1Rbl>/Slc6a3<tm1Rbl>	involves: 129S6/SvEvTac * C57BL/6J	N	24332984
MGI:5643944	M	MP:0002757	decreased vertical activity	Slc6a3<tm1Rbl>/Slc6a3<tm1Rbl>	involves: 129S6/SvEvTac * C57BL/6J	N	25331903
MGI:5643944	M	MP:0004811	abnormal neuron physiology	Slc6a3<tm1Rbl>/Slc6a3<tm1Rbl>	involves: 129S6/SvEvTac * C57BL/6J	N	25331903
MGI:5643950	M	MP:0002757	decreased vertical activity	Slc6a3<tm1Rbl>/Slc6a3<+>	involves: 129S6/SvEvTac * C57BL/6J	N	25331903
MGI:5644332	M	MP:0001360	abnormal social investigation	Wfs1<tm1Yoka>/Wfs1<tm1Yoka>	B6J.129-Wfs1<tm1Yoka>	N	18343518
MGI:5644332	M	MP:0003063	increased coping response	Wfs1<tm1Yoka>/Wfs1<tm1Yoka>	B6J.129-Wfs1<tm1Yoka>	N	18343518
MGI:5644332	M	MP:0001463	abnormal spatial learning	Wfs1<tm1Yoka>/Wfs1<tm1Yoka>	B6J.129-Wfs1<tm1Yoka>	N	18343518
MGI:5644332	M	MP:0003999	enhanced passive avoidance behavior	Wfs1<tm1Yoka>/Wfs1<tm1Yoka>	B6J.129-Wfs1<tm1Yoka>	N	18343518
MGI:5644332	M	MP:0002062	abnormal associative learning	Wfs1<tm1Yoka>/Wfs1<tm1Yoka>	B6J.129-Wfs1<tm1Yoka>	N	18343518
MGI:5644332	M	MP:0003866	abnormal defecation	Wfs1<tm1Yoka>/Wfs1<tm1Yoka>	B6J.129-Wfs1<tm1Yoka>	N	18343518
MGI:5644332	M	MP:0012294	enhanced active avoidance behavior	Wfs1<tm1Yoka>/Wfs1<tm1Yoka>	B6J.129-Wfs1<tm1Yoka>	N	18343518
MGI:5644338	M	MP:0008088	abnormal T-helper 1 cell differentiation	Gpr174<tm1Cys>/Y	B6.129-Gpr174<tm1Cys>	N	26077720
MGI:5644338	M	MP:0005387	immune system phenotype	Gpr174<tm1Cys>/Y	B6.129-Gpr174<tm1Cys>	Y	26077720
MGI:5644338	M	MP:0008082	increased single-positive T cell number	Gpr174<tm1Cys>/Y	B6.129-Gpr174<tm1Cys>	N	26077720
MGI:5644338	M	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis	Gpr174<tm1Cys>/Y	B6.129-Gpr174<tm1Cys>	N	26077720
MGI:5644338	M	MP:0004946	abnormal regulatory T cell physiology	Gpr174<tm1Cys>/Y	B6.129-Gpr174<tm1Cys>	N	26077720
MGI:5644338	M	MP:0005348	increased T cell proliferation	Gpr174<tm1Cys>/Y	B6.129-Gpr174<tm1Cys>	N	26077720
MGI:5644339	F	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis	Gpr174<tm1Cys>/Gpr174<+>	B6.129-Gpr174<tm1Cys>	N	26077720
MGI:5644340	F	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis	Foxp3<tm3(HBEGF/GFP)Ayr>/Foxp3<+>,Gpr174<tm1Cys>/Gpr174<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	26077720
MGI:5644482	F	MP:0009097	absent endometrial glands	Lef1<tm1Rug>/Lef1<tm1Rug>	involves: C57BL/6 * ICR	N	22792274
MGI:5644482	F	MP:0013400	abnormal endometrial gland development	Lef1<tm1Rug>/Lef1<tm1Rug>	involves: C57BL/6 * ICR	N	22792274
MGI:5644488	F	MP:0006270	abnormal mammary gland growth during lactation	Dgat1<tm1Far>/Dgat1<tm1Far>	B6J.129S4-Dgat1<tm1Far>	N	15163627
MGI:5644488	F	MP:0000628	abnormal mammary gland development	Dgat1<tm1Far>/Dgat1<tm1Far>	B6J.129S4-Dgat1<tm1Far>	N	15163627
MGI:5644488	F	MP:0000662	abnormal branching of the mammary ductal tree	Dgat1<tm1Far>/Dgat1<tm1Far>	B6J.129S4-Dgat1<tm1Far>	N	15163627
MGI:5644488	F	MP:0009504	abnormal mammary gland epithelium morphology	Dgat1<tm1Far>/Dgat1<tm1Far>	B6J.129S4-Dgat1<tm1Far>	N	15163627
MGI:5644488	F	MP:0009506	abnormal mammary gland alveolus morphology	Dgat1<tm1Far>/Dgat1<tm1Far>	B6J.129S4-Dgat1<tm1Far>	N	15163627
MGI:5644488	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Dgat1<tm1Far>/Dgat1<tm1Far>	B6J.129S4-Dgat1<tm1Far>	N	15163627
MGI:5644488	F	MP:0004047	abnormal milk composition	Dgat1<tm1Far>/Dgat1<tm1Far>	B6J.129S4-Dgat1<tm1Far>	N	15163627
MGI:5644488	F	MP:0012075	impaired mammary gland growth during pregnancy	Dgat1<tm1Far>/Dgat1<tm1Far>	B6J.129S4-Dgat1<tm1Far>	N	15163627
MGI:5644488	F	MP:0010249	lactation failure	Dgat1<tm1Far>/Dgat1<tm1Far>	B6J.129S4-Dgat1<tm1Far>	N	15163627
MGI:5644488	F	MP:0009297	decreased mammary fat pad weight	Dgat1<tm1Far>/Dgat1<tm1Far>	B6J.129S4-Dgat1<tm1Far>	N	15163627
MGI:5644499	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0013663	increased myeloid cell number	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0001272	increased metastatic potential	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0004973	increased regulatory T cell number	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0008828	abnormal lymph node cell ratio	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0008826	abnormal splenic cell ratio	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0002339	abnormal lymph node morphology	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0005095	decreased T cell proliferation	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0008553	increased circulating tumor necrosis factor level	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0009338	increased splenocyte number	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0009335	decreased splenocyte proliferation	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0005093	decreased B cell proliferation	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0000691	enlarged spleen	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0002444	abnormal T cell physiology	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644499	F	MP:0010210	abnormal circulating cytokine level	Tg(MMTV-PyVT)#Mul/0	B6.FVB-Tg(MMTV-PyVT)#Mul	N	18317964
MGI:5644816	M	MP:0001262	decreased body weight	Dkc1<tm1.1Pjma>/Y	B6.129X1(FVB)-Dkc1<tm1.1Pjma>	N	21241452
MGI:5644816	M	MP:0003674	oxidative stress	Dkc1<tm1.1Pjma>/Y	B6.129X1(FVB)-Dkc1<tm1.1Pjma>	N	21241452
MGI:5644816	M	MP:0005018	decreased T cell number	Dkc1<tm1.1Pjma>/Y	B6.129X1(FVB)-Dkc1<tm1.1Pjma>	N	21241452
MGI:5644816	M	MP:0005017	decreased B cell number	Dkc1<tm1.1Pjma>/Y	B6.129X1(FVB)-Dkc1<tm1.1Pjma>	N	21241452
MGI:5644816	M	MP:0005621	abnormal cell physiology	Dkc1<tm1.1Pjma>/Y	B6.129X1(FVB)-Dkc1<tm1.1Pjma>	N	21241452
MGI:5644816	M	MP:0011903	decreased hematopoietic stem cell proliferation	Dkc1<tm1.1Pjma>/Y	B6.129X1(FVB)-Dkc1<tm1.1Pjma>	N	21241452
MGI:5644816	M	MP:0011704	decreased fibroblast proliferation	Dkc1<tm1.1Pjma>/Y	B6.129X1(FVB)-Dkc1<tm1.1Pjma>	N	21241452
MGI:5645076	M	MP:0002717	abnormal male preputial gland morphology	Cebpa<tm1Gonz>/Cebpa<tm1Gonz>,Cebpb<tm1Es>/Cebpb<tm1Es>,Tg(KRT14-cre/ERT)20Efu/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	20352127
MGI:5646201	F	MP:0004898	uterine hemorrhage	F13a1<tm1Akic>/F13a1<tm1Akic>	involves: 129P2/OlaHsd * Black Swiss	N	18224415
MGI:5646201	F	MP:0008028	pregnancy-related premature death	F13a1<tm1Akic>/F13a1<tm1Akic>	involves: 129P2/OlaHsd * Black Swiss	N	18224415
MGI:5646276	M	MP:0002216	abnormal seminiferous tubule morphology	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0014052	increased male germ cell apoptosis	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0001935	decreased litter size	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0003205	testicular atrophy	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0003674	oxidative stress	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0002675	asthenozoospermia	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0003186	abnormal redox activity	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0004852	decreased testis weight	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0020451	decreased sperm progressive motility	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0001156	abnormal spermatogenesis	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0002662	abnormal cauda epididymis morphology	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0014465	abnormal sperm mitochondrial morphology	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0011632	dilated mitochondrion	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0004851	increased testis weight	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0002687	oligozoospermia	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0014467	increased sperm mitochondrial size	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0004543	abnormal sperm physiology	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0001922	reduced male fertility	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0006379	abnormal spermatocyte morphology	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0005376	homeostasis/metabolism phenotype	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	Y	35469022
MGI:5646276	M	MP:0004901	decreased male germ cell number	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0002685	abnormal spermatogonia proliferation	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646276	M	MP:0006378	abnormal spermatogonia morphology	Lancl1<tm1.1Pfw>/Lancl1<tm1.1Pfw>	involves: 129 * C57BL/6	N	35469022
MGI:5646304	M	MP:0002175	decreased brain weight	Tg(CMV-ATXN3*135Q)CPama/0	C57BL/6-Tg(CMV-ATXN3*135Q)CPama	N	24477711
MGI:5646304	M	MP:0001405	impaired coordination	Tg(CMV-ATXN3*135Q)CPama/0	C57BL/6-Tg(CMV-ATXN3*135Q)CPama	N	24477711
MGI:5646304	M	MP:0001522	impaired swimming	Tg(CMV-ATXN3*135Q)CPama/0	C57BL/6-Tg(CMV-ATXN3*135Q)CPama	N	24477711
MGI:5646304	M	MP:0000774	decreased brain size	Tg(CMV-ATXN3*135Q)CPama/0	C57BL/6-Tg(CMV-ATXN3*135Q)CPama	N	24477711
MGI:5646537	M	MP:0005132	decreased luteinizing hormone level	Npffr1<tm1Lex>/Npffr1<tm1Lex>	involves: 129 * C57BL/6	N	24823392
MGI:5646537	M	MP:0010180	increased susceptibility to weight loss	Npffr1<tm1Lex>/Npffr1<tm1Lex>	involves: 129 * C57BL/6	N	24823392
MGI:5646537	M	MP:0005133	increased luteinizing hormone level	Npffr1<tm1Lex>/Npffr1<tm1Lex>	involves: 129 * C57BL/6	N	24823392
MGI:5648423	M	MP:0005397	hematopoietic system phenotype	Prps2<tm1a(KOMP)Wtsi>/Y	involves: C57BL/6N	Y	24855946
MGI:5648423	M	MP:0002459	abnormal B cell physiology	Prps2<tm1a(KOMP)Wtsi>/Y	involves: C57BL/6N	N	24855946
MGI:5648425	M	MP:0008782	increased B cell apoptosis	Prps2<tm1a(KOMP)Wtsi>/Y,Tg(IghMyc)22Bri/0	involves: C57BL/6N * SJL	N	24855946
MGI:5648425	M	MP:0010769	abnormal survival	Prps2<tm1a(KOMP)Wtsi>/Y,Tg(IghMyc)22Bri/0	involves: C57BL/6N * SJL	N	24855946
MGI:5648425	M	MP:0005397	hematopoietic system phenotype	Prps2<tm1a(KOMP)Wtsi>/Y,Tg(IghMyc)22Bri/0	involves: C57BL/6N * SJL	Y	24855946
MGI:5648425	M	MP:0002459	abnormal B cell physiology	Prps2<tm1a(KOMP)Wtsi>/Y,Tg(IghMyc)22Bri/0	involves: C57BL/6N * SJL	N	24855946
MGI:5648425	M	MP:0009828	increased tumor latency	Prps2<tm1a(KOMP)Wtsi>/Y,Tg(IghMyc)22Bri/0	involves: C57BL/6N * SJL	N	24855946
MGI:5648426	M	MP:0012431	increased lymphoma incidence	Tg(IghMyc)22Bri/0	involves: C57BL/6N * SJL	N	24855946
MGI:5648426	M	MP:0008782	increased B cell apoptosis	Tg(IghMyc)22Bri/0	involves: C57BL/6N * SJL	N	24855946
MGI:5648426	M	MP:0002083	premature death	Tg(IghMyc)22Bri/0	involves: C57BL/6N * SJL	N	24855946
MGI:5659847	F	MP:0001516	abnormal motor coordination/balance	Mto1<Gt(G019A03)Wrst>/Mto1<Gt(G019A03)Wrst>	involves: 129S2/SvPas * C57BL/6J	N	25506927
MGI:5659847	M	MP:0001405	impaired coordination	Mto1<Gt(G019A03)Wrst>/Mto1<Gt(G019A03)Wrst>	involves: 129S2/SvPas * C57BL/6J	N	25506927
MGI:5659902	M	MP:0001262	decreased body weight	Sox9<Bbfc>/Sox9<+>	C57BL/6J-Sox9<Bbfc>/GrsrJ	N	26234751
MGI:5659902	M	MP:0010025	decreased total body fat amount	Sox9<Bbfc>/Sox9<+>	C57BL/6J-Sox9<Bbfc>/GrsrJ	N	26234751
MGI:5659902	M	MP:0000097	short maxilla	Sox9<Bbfc>/Sox9<+>	C57BL/6J-Sox9<Bbfc>/GrsrJ	N	26234751
MGI:5659902	M	MP:0005459	decreased percent body fat/body weight	Sox9<Bbfc>/Sox9<+>	C57BL/6J-Sox9<Bbfc>/GrsrJ	N	26234751
MGI:5660380	M	MP:0005389	reproductive system phenotype	Stk31<tm1.2Jw>/Stk31<tm1.2Jw>	B6J.Cg-Stk31<tm1.2Jw>	Y	24586802
MGI:5660383	M	MP:0005389	reproductive system phenotype	Stk31<tm2Jw>/Stk31<tm2Jw>	B6J.Cg-Stk31<tm2Jw>	Y	24586802
MGI:5660386	M	MP:0009428	decreased tibialis anterior weight	Apobec2<tm1Msn>/Apobec2<tm1Msn>	B6.129P2-Apobec2<tm1Msn>	N	20022958
MGI:5660386	M	MP:0009426	decreased soleus weight	Apobec2<tm1Msn>/Apobec2<tm1Msn>	B6.129P2-Apobec2<tm1Msn>	N	20022958
MGI:5660615	F	MP:0010172	abnormal mammary gland epithelium physiology	Bhlha15<tm1Skz>/Bhlha15<tm1Skz>	involves: 129S6/SvEvTac * C57BL/6	N	16645041
MGI:5660615	F	MP:0009506	abnormal mammary gland alveolus morphology	Bhlha15<tm1Skz>/Bhlha15<tm1Skz>	involves: 129S6/SvEvTac * C57BL/6	N	16645041
MGI:5660615	F	MP:0013781	abnormal mammary gland luminal epithelium morphology	Bhlha15<tm1Skz>/Bhlha15<tm1Skz>	involves: 129S6/SvEvTac * C57BL/6	N	16645041
MGI:5660615	F	MP:0005379	endocrine/exocrine gland phenotype	Bhlha15<tm1Skz>/Bhlha15<tm1Skz>	involves: 129S6/SvEvTac * C57BL/6	Y	16645041
MGI:5660615	F	MP:0014126	increased mammary gland apoptosis	Bhlha15<tm1Skz>/Bhlha15<tm1Skz>	involves: 129S6/SvEvTac * C57BL/6	N	16645041
MGI:5660615	F	MP:0006270	abnormal mammary gland growth during lactation	Bhlha15<tm1Skz>/Bhlha15<tm1Skz>	involves: 129S6/SvEvTac * C57BL/6	N	16645041
MGI:5660617	M	MP:0031134	increased carotid artery tortuosity	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0000414	alopecia	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0008418	abnormal cutaneous elastic fiber morphology	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0001183	overexpanded pulmonary alveolus	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0010996	increased aorta wall thickness	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0009862	abnormal aorta elastic tissue morphology	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0010661	ascending aorta aneurysm	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0009865	abnormal aorta smooth muscle morphology	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0001344	blepharoptosis	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0011575	dilated aorta bulb	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0005421	loose skin	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0000550	abnormal forelimb morphology	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0009869	abnormal descending aorta morphology	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0009867	abnormal ascending aorta morphology	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0000274	enlarged heart	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0031132	increased artery tortuosity	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0010202	focal dorsal hair loss	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0001244	thin dermal layer	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0008438	abnormal cutaneous collagen fibril morphology	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0011643	abnormal tendon collagen fibril morphology	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0001954	respiratory distress	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660617	M	MP:0011157	abnormal hypodermis muscle layer morphology	Efemp2<tm1.1Chu>/Efemp2<tm1.1Chu>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660624	M	MP:0010996	increased aorta wall thickness	Efemp2<tm1.1Chu>/Efemp2<+>	B6(SJL)-Efemp2<tm1.1Chu>	N	26178373
MGI:5660627	M	MP:0004852	decreased testis weight	Sohlh2<tm1Fkh>/Sohlh2<tm1Fkh>	involves: 129S6/SvEvTac * C57BL/6	N	18339773
MGI:5660627	M	MP:0001925	male infertility	Sohlh2<tm1Fkh>/Sohlh2<tm1Fkh>	involves: 129S6/SvEvTac * C57BL/6	N	18339773
MGI:5660627	M	MP:0006379	abnormal spermatocyte morphology	Sohlh2<tm1Fkh>/Sohlh2<tm1Fkh>	involves: 129S6/SvEvTac * C57BL/6	N	18339773
MGI:5660627	M	MP:0003205	testicular atrophy	Sohlh2<tm1Fkh>/Sohlh2<tm1Fkh>	involves: 129S6/SvEvTac * C57BL/6	N	18339773
MGI:5660627	M	MP:0006378	abnormal spermatogonia morphology	Sohlh2<tm1Fkh>/Sohlh2<tm1Fkh>	involves: 129S6/SvEvTac * C57BL/6	N	18339773
MGI:5660627	M	MP:0001147	small testis	Sohlh2<tm1Fkh>/Sohlh2<tm1Fkh>	involves: 129S6/SvEvTac * C57BL/6	N	18339773
MGI:5660627	M	MP:0004901	decreased male germ cell number	Sohlh2<tm1Fkh>/Sohlh2<tm1Fkh>	involves: 129S6/SvEvTac * C57BL/6	N	18339773
MGI:5660627	M	MP:0001155	arrest of spermatogenesis	Sohlh2<tm1Fkh>/Sohlh2<tm1Fkh>	involves: 129S6/SvEvTac * C57BL/6	N	18339773
MGI:5660828	M	MP:0002687	oligozoospermia	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	F	MP:0004856	decreased ovary weight	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	M	MP:0004852	decreased testis weight	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	M	MP:0005189	abnormal anogenital distance	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	F	MP:0002637	small uterus	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	F	MP:0001926	female infertility	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	F	MP:0002636	delayed vaginal opening	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	F	MP:0003969	abnormal luteinizing hormone level	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	F	MP:0001927	abnormal estrous cycle	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	F	MP:0003967	abnormal follicle stimulating hormone level	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	F	MP:0001127	small ovary	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	F	MP:0001134	absent corpus luteum	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	F	MP:0001132	absent mature ovarian follicles	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	M	MP:0003379	absent sexual maturation	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	F	MP:0001931	abnormal oogenesis	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	M	MP:0008940	delayed balanopreputial separation	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	M	MP:0005188	small penis	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660828	M	MP:0001925	male infertility	Kiss1r<tm1.1Hjn>/Kiss1r<tm1.1Hjn>,Tg(Gnrh1-cre)35Awo/0	involves: 129 * C57BL/6 * CD-1	N	24422632
MGI:5660857	M	MP:0002574	increased vertical activity	Nlgn3<tm2.1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ	N	24995986
MGI:5660857	M	MP:0031391	increased locomotor activity	Nlgn3<tm2.1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ	N	24995986
MGI:5660857	M	MP:0012314	enhanced learning	Nlgn3<tm2.1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ	N	24995986
MGI:5660857	M	MP:0001409	increased stereotypic behavior	Nlgn3<tm2.1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ	N	24995986
MGI:5660857	M	MP:0001408	stereotypic behavior	Nlgn3<tm2.1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ	N	24995986
MGI:5660858	M	MP:0014383	decreased miniature inhibitory postsynaptic current frequency	Nlgn3<tm2.1Sud>/Y,Tg(Drd1-tdTomato)5Calak/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24995986
MGI:5660859	M	MP:0012314	enhanced learning	Nlgn3<tm1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ	N	24995986
MGI:5660859	M	MP:0031391	increased locomotor activity	Nlgn3<tm1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ	N	24995986
MGI:5660859	M	MP:0001409	increased stereotypic behavior	Nlgn3<tm1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ	N	24995986
MGI:5660860	M	MP:0014383	decreased miniature inhibitory postsynaptic current frequency	Nlgn3<tm1Sud>/Y,Tg(Drd1-tdTomato)5Calak/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24995986
MGI:5660861	M	MP:0031391	increased locomotor activity	Nlgn3<tm4.1Sud>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24995986
MGI:5660862	M	MP:0031391	increased locomotor activity	Nlgn3<tm4.1Sud>/Y,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24995986
MGI:5660863	M	MP:0001402	decreased locomotor activity	Nlgn3<tm4.1Sud>/Y,Pvalb<tm1(cre)Arbr>/Pvalb<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24995986
MGI:5660864	M	MP:0012314	enhanced learning	Nlgn3<tm4.1Sud>/Y,Tg(Drd1-cre)EY262Gsat/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N * SJL	N	24995986
MGI:5660864	M	MP:0001399	hyperactivity	Nlgn3<tm4.1Sud>/Y,Tg(Drd1-cre)EY262Gsat/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N * SJL	N	24995986
MGI:5660865	M	MP:0005386	behavior/neurological phenotype	Nlgn3<tm4.1Sud>/Y,Tg(Adora2a-cre)2MDkde/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	Y	24995986
MGI:5660866	M	MP:0001409	increased stereotypic behavior	Nlgn3<tm1Sud>/Y,Tg(Drd1-cre)EY262Gsat/0	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	24995986
MGI:5660866	M	MP:0012314	enhanced learning	Nlgn3<tm1Sud>/Y,Tg(Drd1-cre)EY262Gsat/0	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	24995986
MGI:5660867	M	MP:0001399	hyperactivity	Nlgn3<tm4.1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24995986
MGI:5660867	M	MP:0012314	enhanced learning	Nlgn3<tm4.1Sud>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24995986
MGI:5660900	F	MP:0004047	abnormal milk composition	Igfbp7<tm1.1Dds>/Igfbp7<tm1.1Dds>	involves: CD-1	N	24505323
MGI:5660900	F	MP:0013782	abnormal mammary duct terminal end bud morphology	Igfbp7<tm1.1Dds>/Igfbp7<tm1.1Dds>	involves: CD-1	N	24505323
MGI:5660900	F	MP:0006270	abnormal mammary gland growth during lactation	Igfbp7<tm1.1Dds>/Igfbp7<tm1.1Dds>	involves: CD-1	N	24505323
MGI:5660900	F	MP:0006271	abnormal involution of the mammary gland	Igfbp7<tm1.1Dds>/Igfbp7<tm1.1Dds>	involves: CD-1	N	24505323
MGI:5660900	F	MP:0009506	abnormal mammary gland alveolus morphology	Igfbp7<tm1.1Dds>/Igfbp7<tm1.1Dds>	involves: CD-1	N	24505323
MGI:5660900	F	MP:0000662	abnormal branching of the mammary ductal tree	Igfbp7<tm1.1Dds>/Igfbp7<tm1.1Dds>	involves: CD-1	N	24505323
MGI:5660900	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Igfbp7<tm1.1Dds>/Igfbp7<tm1.1Dds>	involves: CD-1	N	24505323
MGI:5660900	F	MP:0000628	abnormal mammary gland development	Igfbp7<tm1.1Dds>/Igfbp7<tm1.1Dds>	involves: CD-1	N	24505323
MGI:5660900	F	MP:0012075	impaired mammary gland growth during pregnancy	Igfbp7<tm1.1Dds>/Igfbp7<tm1.1Dds>	involves: CD-1	N	24505323
MGI:5660926	M	MP:0009745	abnormal behavioral response to xenobiotic	Disc1<tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho>/Disc1<+>	(129S2/SvPasCrl x C57BL)F1	N	24908665
MGI:5660929	M	MP:0009745	abnormal behavioral response to xenobiotic	Disc1<tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho>/Disc1<del>	129S2/SvPasCrl-Disc1<del> Disc1<tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho>	N	24908665
MGI:5660929	M	MP:0001262	decreased body weight	Disc1<tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho>/Disc1<del>	129S2/SvPasCrl-Disc1<del> Disc1<tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho>	N	24908665
MGI:5660929	F	MP:0012347	low sweet preference	Disc1<tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho>/Disc1<del>	129S2/SvPasCrl-Disc1<del> Disc1<tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho>	N	24908665
MGI:5660929	M	MP:0001265	decreased body size	Disc1<tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho>/Disc1<del>	129S2/SvPasCrl-Disc1<del> Disc1<tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho>	N	24908665
MGI:5660929	M	MP:0001577	anemia	Disc1<tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho>/Disc1<del>	129S2/SvPasCrl-Disc1<del> Disc1<tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho>	N	24908665
MGI:5660929	M	MP:0002874	decreased hemoglobin content	Disc1<tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho>/Disc1<del>	129S2/SvPasCrl-Disc1<del> Disc1<tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho>	N	24908665
MGI:5661066	M	MP:0011101	prenatal lethality, incomplete penetrance	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	30647131
MGI:5661066	M	MP:0006092	abnormal olfactory sensory neuron morphology	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	24790208
MGI:5661066	M	MP:0001262	decreased body weight	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	24790208
MGI:5661066	M	MP:0012676	dilated brain ventricle	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	24790208
MGI:5661066	M	MP:0013907	abnormal cerebrospinal fluid flow	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	24790208
MGI:5661066	M	MP:0008544	impaired olfaction	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	24790208
MGI:5661066	M	MP:0001263	weight loss	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	24790208
MGI:5661066	M	MP:0030963	abnormal brain ependyma motile cilium location or orientation	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	24790208
MGI:5661066	M	MP:0005384	cellular phenotype	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	Y	24790208
MGI:5661066	M	MP:0030988	dysosmia	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	24790208
MGI:5661066	M	MP:0001891	hydrocephaly	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	24790208
MGI:5661066	M	MP:0005391	vision/eye phenotype	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	Y	24790208
MGI:5661066	M	MP:0000440	domed cranium	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	24790208
MGI:5661066	M	MP:0011281	abnormal olfactory epithelium cilium morphology	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	24790208
MGI:5661066	M	MP:0002083	premature death	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	24790208
MGI:5661066	M	MP:0000825	dilated lateral ventricle	Cetn2<tm1.1Wbae>/Y	involves: 129 * FVB/N	N	24790208
MGI:5661072	M	MP:0002169	no abnormal phenotype detected	Cetn2<tm1.1Wbae>/Y,Tg(CAG-EGFP/CETN2)3-4Jgg/0	involves: 129 * BALB/c * C57BL/6 * FVB/N	N	24790208
MGI:5661198	F	MP:0001926	female infertility	Ercc2<Mhdarco15>/Ercc2<Mhdarco15>	C3HeB/FeJ-Ercc2<Mhdarco15>	N	25951169
MGI:5661198	M	MP:0005389	reproductive system phenotype	Ercc2<Mhdarco15>/Ercc2<Mhdarco15>	C3HeB/FeJ-Ercc2<Mhdarco15>	Y	25951169
MGI:5661425	F	MP:0001144	vagina atresia	Ankrd6<tm1Pche>/Ankrd6<tm1Pche>,Vangl2<Lp>/Vangl2<+>	involves: 129 * LPT/LeJ	N	25218921
MGI:5661425	F	MP:0001926	female infertility	Ankrd6<tm1Pche>/Ankrd6<tm1Pche>,Vangl2<Lp>/Vangl2<+>	involves: 129 * LPT/LeJ	N	25218921
MGI:5661427	F	MP:0001144	vagina atresia	Vangl2<Lp>/Vangl2<+>	involves: 129 * LPT/LeJ	N	25218921
MGI:5661427	F	MP:0001926	female infertility	Vangl2<Lp>/Vangl2<+>	involves: 129 * LPT/LeJ	N	25218921
MGI:5661462	F	MP:0012307	impaired spatial learning	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	20203623
MGI:5661462	F	MP:0003107	abnormal response to novelty	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	20203623
MGI:5661462	F	MP:0011167	abnormal adipose tissue development	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	24928897
MGI:5661462	F	MP:0004769	abnormal synaptic vesicle morphology	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	20203623
MGI:5661462	F	MP:0005379	endocrine/exocrine gland phenotype	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	Y	24928897
MGI:5661462	F	MP:0008844	decreased subcutaneous adipose tissue amount	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	24928897
MGI:5661462	F	MP:0001262	decreased body weight	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	24928897
MGI:5661462	F	MP:0004792	abnormal synaptic vesicle number	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	20203623
MGI:5661462	F	MP:0004770	abnormal synaptic vesicle recycling	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	20203623
MGI:5661462	F	MP:0005376	homeostasis/metabolism phenotype	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	Y	24928897
MGI:5661462	F	MP:0010025	decreased total body fat amount	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	24928897
MGI:5661462	F	MP:0001525	impaired balance	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	20203623
MGI:5661462	F	MP:0001402	decreased locomotor activity	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	20203623
MGI:5661462	F	MP:0011174	lipodystrophy	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	24928897
MGI:5661462	F	MP:0004793	abnormal synaptic vesicle clustering	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	20203623
MGI:5661462	F	MP:0006320	abnormal interscapular fat pad morphology	Ap1s2<tm1Pschu>/Ap1s2<tm1Pschu>	involves: 129P2/OlaHsd * C57BL/6	N	24928897
MGI:5661468	F	MP:0000662	abnormal branching of the mammary ductal tree	Igfbp7<tm1.1Dds>/Igfbp7<+>	involves: CD-1	N	24505323
MGI:5661468	F	MP:0013782	abnormal mammary duct terminal end bud morphology	Igfbp7<tm1.1Dds>/Igfbp7<+>	involves: CD-1	N	24505323
MGI:5661507	M	MP:0004852	decreased testis weight	Hspbp1<tm1Jhoh>/Hspbp1<tm1Jhoh>	B6.129P2-Hspbp1<tm1Jhoh>	N	24899640
MGI:5661507	M	MP:0001155	arrest of spermatogenesis	Hspbp1<tm1Jhoh>/Hspbp1<tm1Jhoh>	B6.129P2-Hspbp1<tm1Jhoh>	N	24899640
MGI:5661507	M	MP:0002216	abnormal seminiferous tubule morphology	Hspbp1<tm1Jhoh>/Hspbp1<tm1Jhoh>	B6.129P2-Hspbp1<tm1Jhoh>	N	24899640
MGI:5661507	M	MP:0014052	increased male germ cell apoptosis	Hspbp1<tm1Jhoh>/Hspbp1<tm1Jhoh>	B6.129P2-Hspbp1<tm1Jhoh>	N	24899640
MGI:5661507	M	MP:0001147	small testis	Hspbp1<tm1Jhoh>/Hspbp1<tm1Jhoh>	B6.129P2-Hspbp1<tm1Jhoh>	N	24899640
MGI:5661507	M	MP:0004901	decreased male germ cell number	Hspbp1<tm1Jhoh>/Hspbp1<tm1Jhoh>	B6.129P2-Hspbp1<tm1Jhoh>	N	24899640
MGI:5661507	M	MP:0006380	abnormal spermatid morphology	Hspbp1<tm1Jhoh>/Hspbp1<tm1Jhoh>	B6.129P2-Hspbp1<tm1Jhoh>	N	24899640
MGI:5661507	M	MP:0005159	azoospermia	Hspbp1<tm1Jhoh>/Hspbp1<tm1Jhoh>	B6.129P2-Hspbp1<tm1Jhoh>	N	24899640
MGI:5661507	M	MP:0001925	male infertility	Hspbp1<tm1Jhoh>/Hspbp1<tm1Jhoh>	B6.129P2-Hspbp1<tm1Jhoh>	N	24899640
MGI:5661507	M	MP:0008261	arrest of male meiosis	Hspbp1<tm1Jhoh>/Hspbp1<tm1Jhoh>	B6.129P2-Hspbp1<tm1Jhoh>	N	24899640
MGI:5661879	F	MP:0009453	enhanced contextual conditioning behavior	Comt<tm1(COMT)Xzho>/Comt<tm1(COMT)Xzho>	involves: 129 * C57BL/6J	N	24509724
MGI:5661879	F	MP:0009456	impaired cued conditioning behavior	Comt<tm1(COMT)Xzho>/Comt<tm1(COMT)Xzho>	involves: 129 * C57BL/6J	N	24509724
MGI:5661879	F	MP:0009141	increased prepulse inhibition	Comt<tm1(COMT)Xzho>/Comt<tm1(COMT)Xzho>	involves: 129 * C57BL/6J	N	24509724
MGI:5661879	M	MP:0005386	behavior/neurological phenotype	Comt<tm1(COMT)Xzho>/Comt<tm1(COMT)Xzho>	involves: 129 * C57BL/6J	Y	24509724
MGI:5661879	M	MP:0001488	increased startle reflex	Comt<tm1(COMT)Xzho>/Comt<tm1(COMT)Xzho>	involves: 129 * C57BL/6J	N	24509724
MGI:5661879	M	MP:0009142	decreased prepulse inhibition	Comt<tm1(COMT)Xzho>/Comt<tm1(COMT)Xzho>	involves: 129 * C57BL/6J	N	24509724
MGI:5661879	F	MP:0002757	decreased vertical activity	Comt<tm1(COMT)Xzho>/Comt<tm1(COMT)Xzho>	involves: 129 * C57BL/6J	N	24509724
MGI:5661880	F	MP:0003106	abnormal fear-related response	Comt<tm2(COMT)Xzho>/Comt<tm2(COMT)Xzho>	involves: 129 * C57BL/6J	N	24509724
MGI:5661880	F	MP:0009142	decreased prepulse inhibition	Comt<tm2(COMT)Xzho>/Comt<tm2(COMT)Xzho>	involves: 129 * C57BL/6J	N	24509724
MGI:5661880	M	MP:0001489	decreased startle reflex	Comt<tm2(COMT)Xzho>/Comt<tm2(COMT)Xzho>	involves: 129 * C57BL/6J	N	24509724
MGI:5661880	F	MP:0002574	increased vertical activity	Comt<tm2(COMT)Xzho>/Comt<tm2(COMT)Xzho>	involves: 129 * C57BL/6J	N	24509724
MGI:5661880	F	MP:0009455	enhanced cued conditioning behavior	Comt<tm2(COMT)Xzho>/Comt<tm2(COMT)Xzho>	involves: 129 * C57BL/6J	N	24509724
MGI:5661880	F	MP:0009454	impaired contextual conditioning behavior	Comt<tm2(COMT)Xzho>/Comt<tm2(COMT)Xzho>	involves: 129 * C57BL/6J	N	24509724
MGI:5661880	M	MP:0009141	increased prepulse inhibition	Comt<tm2(COMT)Xzho>/Comt<tm2(COMT)Xzho>	involves: 129 * C57BL/6J	N	24509724
MGI:5661932	M	MP:0009745	abnormal behavioral response to xenobiotic	Baiap3<tm1Smwk>/Baiap3<tm1Smwk>	B6N.129P2-Baiap3<tm1Smwk>	N	23698091
MGI:5661932	F	MP:0002797	increased thigmotaxis	Baiap3<tm1Smwk>/Baiap3<tm1Smwk>	B6N.129P2-Baiap3<tm1Smwk>	N	23698091
MGI:5662240	F	MP:0004898	uterine hemorrhage	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	B6.Cg-Ggcx<tm1Sinos> Speer6-ps1<Tg(Alb-cre)21Mgn>	N	24520408
MGI:5662240	F	MP:0008028	pregnancy-related premature death	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	B6.Cg-Ggcx<tm1Sinos> Speer6-ps1<Tg(Alb-cre)21Mgn>	N	24520408
MGI:5662267	F	MP:0001935	decreased litter size	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0020011	increased bone mineral density of femur	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	25211588
MGI:5662267	F	MP:0031420	decreased superovulation rate	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0001927	abnormal estrous cycle	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0013508	increased granulosa cell apoptosis	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0009444	ovarian follicular cyst	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0031239	increased atretic ovarian follicle number	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0009006	prolonged estrous cycle	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	25211588
MGI:5662267	F	MP:0005331	insulin resistance	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	25211588
MGI:5662267	F	MP:0002781	increased circulating testosterone level	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	25211588
MGI:5662267	F	MP:0010123	increased bone mineral content	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	25211588
MGI:5662267	F	MP:0009012	short diestrus	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0005293	impaired glucose tolerance	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	25211588
MGI:5662267	F	MP:0009012	short diestrus	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	25211588
MGI:5662267	F	MP:0009648	abnormal superovulation	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0005185	decreased circulating progesterone level	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0002079	increased circulating insulin level	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	25211588
MGI:5662267	F	MP:0009017	prolonged estrus	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0003953	abnormal hormone level	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0003960	increased lean body mass	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	25211588
MGI:5662267	F	MP:0003377	late onset of menarche	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0002184	abnormal innervation	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0001260	increased body weight	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	25211588
MGI:5662267	F	MP:0005182	increased circulating estradiol level	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	25211588
MGI:5662267	F	MP:0001923	reduced female fertility	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0009363	abnormal tertiary ovarian follicle morphology	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0010024	increased total body fat amount	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	25211588
MGI:5662267	F	MP:0001938	delayed sexual maturation	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662267	F	MP:0004183	abnormal sympathetic nervous system physiology	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	25211588
MGI:5662267	F	MP:0001129	impaired ovarian folliculogenesis	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje	involves: C57BL/6J * DBA/2J	N	19264868
MGI:5662389	M	MP:0009936	abnormal dendritic spine morphology	Del(5Gtf2i-Fkbp6)1Vcam/+	B6.129-Del(5Gtf2i-Fkbp6)1Vcam(J:204278)	N	25027326
MGI:5662389	M	MP:0030981	abnormal dentate gyrus subgranular zone morphology	Del(5Gtf2i-Fkbp6)1Vcam/+	B6.129-Del(5Gtf2i-Fkbp6)1Vcam(J:204278)	N	25027326
MGI:5662389	M	MP:0004262	abnormal physical strength	Del(5Gtf2i-Fkbp6)1Vcam/+	B6.129-Del(5Gtf2i-Fkbp6)1Vcam(J:204278)	N	25027326
MGI:5662389	M	MP:0000818	abnormal amygdala morphology	Del(5Gtf2i-Fkbp6)1Vcam/+	B6.129-Del(5Gtf2i-Fkbp6)1Vcam(J:204278)	N	25027326
MGI:5662389	M	MP:0008143	abnormal dendrite morphology	Del(5Gtf2i-Fkbp6)1Vcam/+	B6.129-Del(5Gtf2i-Fkbp6)1Vcam(J:204278)	N	25027326
MGI:5688286	M	MP:0010313	increased osteoma incidence	Apc<M1Tno>/Apc<+>	involves: C57BL/6 * DBA/2JJcl	N	23551873
MGI:5688286	F	MP:0010299	increased mammary gland tumor incidence	Apc<M1Tno>/Apc<+>	involves: C57BL/6 * DBA/2JJcl	N	23551873
MGI:5688385	M	MP:0001925	male infertility	Ccnyl1<tm1a(EUCOMM)Wtsi>/Ccnyl1<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	26305884
MGI:5688385	M	MP:0009834	abnormal sperm annulus morphology	Ccnyl1<tm1a(EUCOMM)Wtsi>/Ccnyl1<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	26305884
MGI:5688385	M	MP:0009833	absent sperm mitochondrial sheath	Ccnyl1<tm1a(EUCOMM)Wtsi>/Ccnyl1<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	26305884
MGI:5688385	M	MP:0020451	decreased sperm progressive motility	Ccnyl1<tm1a(EUCOMM)Wtsi>/Ccnyl1<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	26305884
MGI:5688385	M	MP:0005578	teratozoospermia	Ccnyl1<tm1a(EUCOMM)Wtsi>/Ccnyl1<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	26305884
MGI:5688385	F	MP:0005389	reproductive system phenotype	Ccnyl1<tm1a(EUCOMM)Wtsi>/Ccnyl1<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	Y	26305884
MGI:5688385	M	MP:0000242	impaired fertilization	Ccnyl1<tm1a(EUCOMM)Wtsi>/Ccnyl1<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	26305884
MGI:5688385	M	MP:0002675	asthenozoospermia	Ccnyl1<tm1a(EUCOMM)Wtsi>/Ccnyl1<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	26305884
MGI:5688471	M	MP:0014052	increased male germ cell apoptosis	Fancb<em1Shnk>/Fancb<em1Shnk>	C57BL/6J-Fancb<em1Shnk>	N	26123487
MGI:5688471	M	MP:0002776	increased Sertoli cell number	Fancb<em1Shnk>/Fancb<em1Shnk>	C57BL/6J-Fancb<em1Shnk>	N	26123487
MGI:5688471	M	MP:0001925	male infertility	Fancb<em1Shnk>/Fancb<em1Shnk>	C57BL/6J-Fancb<em1Shnk>	N	26123487
MGI:5688471	M	MP:0008392	decreased primordial germ cell number	Fancb<em1Shnk>/Fancb<em1Shnk>	C57BL/6J-Fancb<em1Shnk>	N	26123487
MGI:5688471	M	MP:0002687	oligozoospermia	Fancb<em1Shnk>/Fancb<em1Shnk>	C57BL/6J-Fancb<em1Shnk>	N	26123487
MGI:5688471	M	MP:0006378	abnormal spermatogonia morphology	Fancb<em1Shnk>/Fancb<em1Shnk>	C57BL/6J-Fancb<em1Shnk>	N	26123487
MGI:5688471	M	MP:0001154	seminiferous tubule degeneration	Fancb<em1Shnk>/Fancb<em1Shnk>	C57BL/6J-Fancb<em1Shnk>	N	26123487
MGI:5688471	M	MP:0010948	abnormal double-strand DNA break repair	Fancb<em1Shnk>/Fancb<em1Shnk>	C57BL/6J-Fancb<em1Shnk>	N	26123487
MGI:5688471	M	MP:0006380	abnormal spermatid morphology	Fancb<em1Shnk>/Fancb<em1Shnk>	C57BL/6J-Fancb<em1Shnk>	N	26123487
MGI:5688471	M	MP:0001153	small seminiferous tubules	Fancb<em1Shnk>/Fancb<em1Shnk>	C57BL/6J-Fancb<em1Shnk>	N	26123487
MGI:5688471	M	MP:0004901	decreased male germ cell number	Fancb<em1Shnk>/Fancb<em1Shnk>	C57BL/6J-Fancb<em1Shnk>	N	26123487
MGI:5688471	M	MP:0001147	small testis	Fancb<em1Shnk>/Fancb<em1Shnk>	C57BL/6J-Fancb<em1Shnk>	N	26123487
MGI:5688487	M	MP:0002833	increased heart weight	Wdr1<tm1.1Zzy>/Wdr1<tm1.1Zzy>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S6/SvEvTac * C57BL/6J	N	24840128
MGI:5688495	F	MP:0000063	decreased bone mineral density	Tg(SFTPC-Il18)AThos/0	B6N.Cg-Tg(SFTPC-Il18)AThos	N	24565845
MGI:5688495	F	MP:0005293	impaired glucose tolerance	Tg(SFTPC-Il18)AThos/0	B6N.Cg-Tg(SFTPC-Il18)AThos	N	24565845
MGI:5688495	F	MP:0010239	decreased skeletal muscle weight	Tg(SFTPC-Il18)AThos/0	B6N.Cg-Tg(SFTPC-Il18)AThos	N	24565845
MGI:5688495	F	MP:0001263	weight loss	Tg(SFTPC-Il18)AThos/0	B6N.Cg-Tg(SFTPC-Il18)AThos	N	24565845
MGI:5688502	F	MP:0005390	skeleton phenotype	Il13<tm2Anjm>/Il13<tm2Anjm>,Tg(SFTPC-Il18)AThos/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N * DBA/2	Y	24565845
MGI:5688502	F	MP:0001263	weight loss	Il13<tm2Anjm>/Il13<tm2Anjm>,Tg(SFTPC-Il18)AThos/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N * DBA/2	N	24565845
MGI:5688502	F	MP:0010239	decreased skeletal muscle weight	Il13<tm2Anjm>/Il13<tm2Anjm>,Tg(SFTPC-Il18)AThos/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N * DBA/2	N	24565845
MGI:5688693	F	MP:0000630	mammary gland hyperplasia	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(MMTV-cre)#Tfln/0	involves: 129S4/SvJae	N	12163417
MGI:5688693	F	MP:0009505	abnormal mammary gland lobule morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(MMTV-cre)#Tfln/0	involves: 129S4/SvJae	N	12163417
MGI:5688693	F	MP:0001885	mammary gland duct hyperplasia	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(MMTV-cre)#Tfln/0	involves: 129S4/SvJae	N	12163417
MGI:5688693	F	MP:0006269	abnormal mammary gland growth during pregnancy	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(MMTV-cre)#Tfln/0	involves: 129S4/SvJae	N	12163417
MGI:5688693	F	MP:0009504	abnormal mammary gland epithelium morphology	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(MMTV-cre)#Tfln/0	involves: 129S4/SvJae	N	12163417
MGI:5688693	F	MP:0000662	abnormal branching of the mammary ductal tree	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(MMTV-cre)#Tfln/0	involves: 129S4/SvJae	N	12163417
MGI:5688693	F	MP:0006271	abnormal involution of the mammary gland	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(MMTV-cre)#Tfln/0	involves: 129S4/SvJae	N	12163417
MGI:5688714	F	MP:0001926	female infertility	Meikin<tm1Yow>/Meikin<tm1Yow>	involves: C57BL/6	N	25533956
MGI:5688714	F	MP:0014443	impaired polar body extrusion	Meikin<tm1Yow>/Meikin<tm1Yow>	involves: C57BL/6	N	25533956
MGI:5688714	M	MP:0006380	abnormal spermatid morphology	Meikin<tm1Yow>/Meikin<tm1Yow>	involves: C57BL/6	N	25533956
MGI:5688714	M	MP:0008261	arrest of male meiosis	Meikin<tm1Yow>/Meikin<tm1Yow>	involves: C57BL/6	N	25533956
MGI:5688714	M	MP:0002687	oligozoospermia	Meikin<tm1Yow>/Meikin<tm1Yow>	involves: C57BL/6	N	25533956
MGI:5688714	M	MP:0001925	male infertility	Meikin<tm1Yow>/Meikin<tm1Yow>	involves: C57BL/6	N	25533956
MGI:5688714	F	MP:0005168	abnormal female meiosis	Meikin<tm1Yow>/Meikin<tm1Yow>	involves: C57BL/6	N	25533956
MGI:5688714	M	MP:0005169	abnormal male meiosis	Meikin<tm1Yow>/Meikin<tm1Yow>	involves: C57BL/6	N	25533956
MGI:5688778	M	MP:0001405	impaired coordination	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688778	M	MP:0002826	tonic seizures	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688778	M	MP:0013438	dysmyelination	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688778	M	MP:0000953	abnormal oligodendrocyte morphology	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688778	M	MP:0000745	tremors	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688778	M	MP:0010205	abnormal oligodendrocyte apoptosis	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688778	M	MP:0005405	axon degeneration	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688778	M	MP:0030987	spinal cord inflammation	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688778	M	MP:0002083	premature death	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688778	M	MP:0001406	abnormal gait	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688778	M	MP:0003354	astrocytosis	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688778	M	MP:0000921	demyelination	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688778	M	MP:0008918	microgliosis	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688778	M	MP:0030991	optic nerve inflammation	Gjb1<tm1Kwi>/Y,Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	N	25524707
MGI:5688978	M	MP:0004217	salt-sensitive hypertension	Map3k15<tm1Hijo>/Y	involves: C57BL/6 * ICR	N	23250415
MGI:5688978	M	MP:0002136	abnormal kidney physiology	Map3k15<tm1Hijo>/Y	involves: C57BL/6 * ICR	N	23250415
MGI:5688978	M	MP:0006144	increased systemic arterial systolic blood pressure	Map3k15<tm1Hijo>/Y	involves: C57BL/6 * ICR	N	23250415
MGI:5688978	M	MP:0000231	hypertension	Map3k15<tm1Hijo>/Y	involves: C57BL/6 * ICR	N	23250415
MGI:5688978	M	MP:0005621	abnormal cell physiology	Map3k15<tm1Hijo>/Y	involves: C57BL/6 * ICR	N	23250415
MGI:5688978	M	MP:0005376	homeostasis/metabolism phenotype	Map3k15<tm1Hijo>/Y	involves: C57BL/6 * ICR	Y	23250415
MGI:5689167	F	MP:0012411	increased granulosa cell tumor incidence	Bap1<em1Test>/Bap1<+>	involves: FVB	N	26896281
MGI:5689167	F	MP:0008000	increased ovary tumor incidence	Bap1<em1Test>/Bap1<+>	involves: FVB	N	26896281
MGI:5689329	M	MP:0014365	impaired short-term object recognition memory	Dtnbp1<sdy>/Dtnbp1<+>	DBA/2J-Dtnbp1<sdy>/J	N	18984010
MGI:5689329	M	MP:0003043	hypoalgesia	Dtnbp1<sdy>/Dtnbp1<+>	DBA/2J-Dtnbp1<sdy>/J	N	18984010
MGI:5689331	M	MP:0002803	abnormal operant conditioning behavior	Dtnbp1<sdy>/Dtnbp1<sdy>	B6J.D2-Dtnbp1<sdy>	N	23261874
MGI:5689331	M	MP:0009142	decreased prepulse inhibition	Dtnbp1<sdy>/Dtnbp1<sdy>	B6J.D2-Dtnbp1<sdy>	N	25677649
MGI:5689331	M	MP:0005376	homeostasis/metabolism phenotype	Dtnbp1<sdy>/Dtnbp1<sdy>	B6J.D2-Dtnbp1<sdy>	Y	25677649
MGI:5689331	M	MP:0031391	increased locomotor activity	Dtnbp1<sdy>/Dtnbp1<sdy>	B6J.D2-Dtnbp1<sdy>	N	25677649
MGI:5689331	M	MP:0020467	abnormal circadian behavior	Dtnbp1<sdy>/Dtnbp1<sdy>	B6J.D2-Dtnbp1<sdy>	N	25677649
MGI:5689331	M	MP:0001364	decreased anxiety-related response	Dtnbp1<sdy>/Dtnbp1<sdy>	B6J.D2-Dtnbp1<sdy>	N	25677649
MGI:5689832	M	MP:0020088	decreased susceptibility to non-insulin-dependent diabetes	Alox15<tm1.1Nadl>/Alox15<tm1.1Nadl>,Tg(Pdx1-cre)89.1Dam/0	involves: C57BL/6 * CBA	N	25071151
MGI:5689835	M	MP:0003088	abnormal prepulse inhibition	Reln<rl>/Reln<+>	B6.Cg-Reln<rl>	N	25845740
MGI:5689835	M	MP:0001360	abnormal social investigation	Reln<rl>/Reln<+>	B6.Cg-Reln<rl>	N	25845740
MGI:5690104	M	MP:0001925	male infertility	Scml2<em1Shnk>/Scml2<em1Shnk>	C57BL/6J-Scml2<em1Shnk>	N	25703348
MGI:5690104	M	MP:0001147	small testis	Scml2<em1Shnk>/Scml2<em1Shnk>	C57BL/6J-Scml2<em1Shnk>	N	25703348
MGI:5690104	M	MP:0005159	azoospermia	Scml2<em1Shnk>/Scml2<em1Shnk>	C57BL/6J-Scml2<em1Shnk>	N	25703348
MGI:5690104	M	MP:0020550	multinucleated giant male germ cells	Scml2<em1Shnk>/Scml2<em1Shnk>	C57BL/6J-Scml2<em1Shnk>	N	25703348
MGI:5690104	M	MP:0014052	increased male germ cell apoptosis	Scml2<em1Shnk>/Scml2<em1Shnk>	C57BL/6J-Scml2<em1Shnk>	N	25703348
MGI:5690104	M	MP:0001932	abnormal spermiogenesis	Scml2<em1Shnk>/Scml2<em1Shnk>	C57BL/6J-Scml2<em1Shnk>	N	25703348
MGI:5690106	M	MP:0014052	increased male germ cell apoptosis	Scml2<em2Shnk>/Scml2<em2Shnk>	C57BL/6J-Scml2<em2Shnk>	N	25703348
MGI:5690106	M	MP:0001932	abnormal spermiogenesis	Scml2<em2Shnk>/Scml2<em2Shnk>	C57BL/6J-Scml2<em2Shnk>	N	25703348
MGI:5690106	M	MP:0005159	azoospermia	Scml2<em2Shnk>/Scml2<em2Shnk>	C57BL/6J-Scml2<em2Shnk>	N	25703348
MGI:5690106	M	MP:0001147	small testis	Scml2<em2Shnk>/Scml2<em2Shnk>	C57BL/6J-Scml2<em2Shnk>	N	25703348
MGI:5690106	M	MP:0001925	male infertility	Scml2<em2Shnk>/Scml2<em2Shnk>	C57BL/6J-Scml2<em2Shnk>	N	25703348
MGI:5690106	M	MP:0020550	multinucleated giant male germ cells	Scml2<em2Shnk>/Scml2<em2Shnk>	C57BL/6J-Scml2<em2Shnk>	N	25703348
MGI:5690107	M	MP:0006431	abnormal fibrocartilage morphology	Clec4a2<tm1Yiw>/Clec4a2<tm1Yiw>	involves: 129P2/OlaHsd * C57BL/6J	N	18204462
MGI:5690107	M	MP:0020039	increased bone ossification	Clec4a2<tm1Yiw>/Clec4a2<tm1Yiw>	involves: 129P2/OlaHsd * C57BL/6J	N	18204462
MGI:5691397	M	MP:0009355	increased liver triglyceride level	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0004889	increased energy expenditure	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0003927	increased cellular glucose import	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0003887	increased hepatocyte apoptosis	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0009125	decreased brown fat cell lipid droplet size	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0002941	increased circulating alanine transaminase level	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0009122	decreased white fat cell lipid droplet size	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0008963	increased carbon dioxide production	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0001263	weight loss	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0010398	decreased liver glycogen level	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0002628	hepatic steatosis	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0002118	abnormal lipid homeostasis	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0001402	decreased locomotor activity	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0005584	abnormal enzyme/coenzyme activity	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0005289	increased oxygen consumption	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0005292	improved glucose tolerance	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0009746	enhanced behavioral response to xenobiotic	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0005459	decreased percent body fat/body weight	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0000609	abnormal liver physiology	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0000599	enlarged liver	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0001262	decreased body weight	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0002981	increased liver weight	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0005384	cellular phenotype	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	Y	25043815
MGI:5691397	M	MP:0020103	decreased hepatic glucose production	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0010378	increased respiratory quotient	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0005455	increased susceptibility to weight gain	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0013278	decreased fasting circulating glucose level	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0002078	abnormal glucose homeostasis	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0008260	abnormal autophagy	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0009283	decreased gonadal fat pad weight	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0000603	pale liver	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691397	M	MP:0003325	decreased liver function	Lamp2<tm1Amcu>/Y,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	25043815
MGI:5691432	M	MP:0001154	seminiferous tubule degeneration	Faap20<tm1(KOMP)Mbp>/Faap20<tm1(KOMP)Mbp>	involves: C57BL/6 * C57BL/6N	N	25917546
MGI:5691432	M	MP:0004901	decreased male germ cell number	Faap20<tm1(KOMP)Mbp>/Faap20<tm1(KOMP)Mbp>	involves: C57BL/6 * C57BL/6N	N	25917546
MGI:5691432	F	MP:0001127	small ovary	Faap20<tm1(KOMP)Mbp>/Faap20<tm1(KOMP)Mbp>	involves: C57BL/6 * C57BL/6N	N	25917546
MGI:5691432	M	MP:0001147	small testis	Faap20<tm1(KOMP)Mbp>/Faap20<tm1(KOMP)Mbp>	involves: C57BL/6 * C57BL/6N	N	25917546
MGI:5691432	F	MP:0001131	abnormal ovarian follicle morphology	Faap20<tm1(KOMP)Mbp>/Faap20<tm1(KOMP)Mbp>	involves: C57BL/6 * C57BL/6N	N	25917546
MGI:5691444	M	MP:0003313	abnormal locomotor activation	Fosb<tm1.1Yun>/Fosb<tm1.1Yun>	B6.129S-Fosb<tm1.1Yun>	N	21679928
MGI:5691444	M	MP:0001415	increased exploration in new environment	Fosb<tm1.1Yun>/Fosb<tm1.1Yun>	B6.129S-Fosb<tm1.1Yun>	N	21679928
MGI:5691444	M	MP:0031391	increased locomotor activity	Fosb<tm1.1Yun>/Fosb<tm1.1Yun>	B6.129S-Fosb<tm1.1Yun>	N	21679928
MGI:5691444	M	MP:0001364	decreased anxiety-related response	Fosb<tm1.1Yun>/Fosb<tm1.1Yun>	B6.129S-Fosb<tm1.1Yun>	N	21679928
MGI:5691445	M	MP:0001415	increased exploration in new environment	Fosb<tm1.1Yun>/Fosb<+>	B6.129S-Fosb<tm1.1Yun>	N	21679928
MGI:5691445	M	MP:0003313	abnormal locomotor activation	Fosb<tm1.1Yun>/Fosb<+>	B6.129S-Fosb<tm1.1Yun>	N	21679928
MGI:5691445	M	MP:0001364	decreased anxiety-related response	Fosb<tm1.1Yun>/Fosb<+>	B6.129S-Fosb<tm1.1Yun>	N	21679928
MGI:5691445	M	MP:0031391	increased locomotor activity	Fosb<tm1.1Yun>/Fosb<+>	B6.129S-Fosb<tm1.1Yun>	N	21679928
MGI:5691446	M	MP:0001363	increased anxiety-related response	Fosb<tm2.1Yun>/Fosb<tm2.1Yun>	involves: 129S/SvEv * C57BL/6	N	21679928
MGI:5691446	M	MP:0002063	abnormal learning/memory/conditioning	Fosb<tm2.1Yun>/Fosb<tm2.1Yun>	involves: 129S/SvEv * C57BL/6	N	21679928
MGI:5691446	M	MP:0003313	abnormal locomotor activation	Fosb<tm2.1Yun>/Fosb<tm2.1Yun>	involves: 129S/SvEv * C57BL/6	N	21679928
MGI:5691446	M	MP:0001415	increased exploration in new environment	Fosb<tm2.1Yun>/Fosb<tm2.1Yun>	involves: 129S/SvEv * C57BL/6	N	21679928
MGI:5691446	M	MP:0012307	impaired spatial learning	Fosb<tm2.1Yun>/Fosb<tm2.1Yun>	involves: 129S/SvEv * C57BL/6	N	21679928
MGI:5691446	M	MP:0003360	abnormal depression-related behavior	Fosb<tm2.1Yun>/Fosb<tm2.1Yun>	involves: 129S/SvEv * C57BL/6	N	21679928
MGI:5691446	M	MP:0031391	increased locomotor activity	Fosb<tm2.1Yun>/Fosb<tm2.1Yun>	involves: 129S/SvEv * C57BL/6	N	21679928
MGI:5691446	M	MP:0002572	abnormal emotion/affect behavior	Fosb<tm2.1Yun>/Fosb<tm2.1Yun>	involves: 129S/SvEv * C57BL/6	N	21679928
MGI:5691447	M	MP:0003313	abnormal locomotor activation	Fosb<tm2.1Yun>/Fosb<+>	involves: 129S/SvEv * C57BL/6	N	21679928
MGI:5691737	F	MP:0005459	decreased percent body fat/body weight	Pfas<Sofa-3J>/Pfas<+>	B6(129S7)-Pfas<Sofa-3J>/GrsrJ	N	26234751
MGI:5691774	M	MP:0005459	decreased percent body fat/body weight	Pfas<Sofa-4J>/Pfas<+>	C57BL/6J-Pfas<Sofa-4J>/GrsrJ	N	26234751
MGI:5691774	M	MP:0010025	decreased total body fat amount	Pfas<Sofa-4J>/Pfas<+>	C57BL/6J-Pfas<Sofa-4J>/GrsrJ	N	26234751
MGI:5691774	M	MP:0006086	decreased body mass index	Pfas<Sofa-4J>/Pfas<+>	C57BL/6J-Pfas<Sofa-4J>/GrsrJ	N	26234751
MGI:5691952	F	MP:0002083	premature death	Hmgcr<tm2Ishi>/Hmgcr<tm2Ishi>,Tg(Alb1-cre)1Dlr/0	involves: 129S7/SvEvBrd * C57BL/6J	N	22701022
MGI:5691953	F	MP:0001405	impaired coordination	Tbp<tm1Xjl>/Tbp<tm1Xjl>,Tg(Nes-cre)1Kln/?	involves: 129S/SvEv * C57BL/6 * SJL	N	21705419
MGI:5692156	F	MP:0003329	amyloid beta deposits	Agrn<tm1Rwb>/Agrn<tm1Rwb>,Tg(APPswe,PSEN1dE9)85Dbo/?,Tg(Tek-cre)1Ywa/?	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 * SJL	N	22082664
MGI:5692162	M	MP:0003329	amyloid beta deposits	Tg(APPswe,PSEN1dE9)85Dbo/?,Tg(MGS1-19375/CFP)2R9Rwb/?	involves: C3H * C57BL/6 * C57BL/6J	N	22082664
MGI:5692282	F	MP:0011121	decreased primordial ovarian follicle number	Sycp2l<tm1Jw>/Sycp2l<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	26362258
MGI:5692282	F	MP:0031381	decreased secondary ovarian follicle number	Sycp2l<tm1Jw>/Sycp2l<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	26362258
MGI:5692282	F	MP:0001935	decreased litter size	Sycp2l<tm1Jw>/Sycp2l<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	26362258
MGI:5692282	F	MP:0011125	decreased primary ovarian follicle number	Sycp2l<tm1Jw>/Sycp2l<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	26362258
MGI:5692282	F	MP:0008995	early reproductive senescence	Sycp2l<tm1Jw>/Sycp2l<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	26362258
MGI:5692282	F	MP:0001923	reduced female fertility	Sycp2l<tm1Jw>/Sycp2l<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	26362258
MGI:5692282	F	MP:0005431	decreased oocyte number	Sycp2l<tm1Jw>/Sycp2l<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	26362258
MGI:5692454	F	MP:0011400	lethality, complete penetrance	Eef1a1<tm1Tcrl>/Eef1a1<tm1Tcrl>	involves: 129S6/SvEvTac * C57BL/6	N	25809849
MGI:5693392	M	MP:0003409	decreased width of hypertrophic chondrocyte zone	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0006322	abnormal perichondrium morphology	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0003419	delayed endochondral bone ossification	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0013258	abnormal extracellular matrix morphology	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0003420	delayed intramembranous bone ossification	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0002115	abnormal limb bone morphology	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0000154	rib fusion	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0000074	abnormal neurocranium morphology	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0003566	abnormal cell adhesion	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0008489	slow postnatal weight gain	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0008155	decreased diameter of radius	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0008157	decreased diameter of ulna	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0004674	thin ribs	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	F	MP:0030797	joint laxity	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0000166	abnormal chondrocyte morphology	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0004355	short radius	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0009780	abnormal chondrocyte physiology	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0000161	scoliosis	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0011110	preweaning lethality, incomplete penetrance	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0000162	lordosis	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0002113	abnormal skeleton development	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0000063	decreased bone mineral density	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0000160	kyphosis	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	F	MP:0004609	vertebral fusion	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0001732	postnatal growth retardation	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0000060	delayed bone ossification	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0002543	brachyphalangia	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0003662	abnormal long bone epiphyseal plate proliferative zone	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0005353	abnormal patella morphology	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0000552	abnormal radius morphology	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0005108	abnormal ulna morphology	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0004624	abnormal thoracic cage morphology	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0004620	cervical vertebral fusion	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0020137	decreased bone mineralization	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0006396	decreased long bone epiphyseal plate size	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0010103	small thoracic cage	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0020040	decreased bone ossification	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0005269	abnormal occipital bone morphology	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0005274	abnormal viscerocranium morphology	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0014289	decreased distal limb length	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693392	M	MP:0000109	abnormal parietal bone morphology	Flnb<tm1Vshn>/Flnb<tm1Vshn>	involves: 129S6/SvEvTac * C57BL/6	N	17510210
MGI:5693869	M	MP:0003698	abnormal male reproductive system physiology	Tcam1<tm1Zuk>/Tcam1<tm1Zuk>	involves: 129S4/SvJaeSor * 129S5/SvEvBrd	N	19766163
MGI:5693870	M	MP:0005389	reproductive system phenotype	Tcam1<tm1Zuk>/Tcam1<tm1Zuk>	involves: 129S4/SvJaeSor * C57BL/6	Y	19766163
MGI:5693911	F	MP:0010124	decreased bone mineral content	Ddx10<m1J>/Ddx10<m1J>	B6;129S1-Ddx10<m1J>/GrsrJ	N	26234751
MGI:5693911	F	MP:0013618	decreased areal bone mineral density	Ddx10<m1J>/Ddx10<m1J>	B6;129S1-Ddx10<m1J>/GrsrJ	N	26234751
MGI:5694070	M	MP:0011862	decreased cranium length	Rdns/Rdns<+>	C57BL/6J-Rdns/GrsrJ	N	26234751
MGI:5694070	M	MP:0030166	increased inner canthal distance	Rdns/Rdns<+>	C57BL/6J-Rdns/GrsrJ	N	26234751
MGI:5694070	F	MP:0001935	decreased litter size	Rdns/Rdns<+>	C57BL/6J-Rdns/GrsrJ	N	26234751
MGI:5694070	M	MP:0000097	short maxilla	Rdns/Rdns<+>	C57BL/6J-Rdns/GrsrJ	N	26234751
MGI:5694075	M	MP:0004924	abnormal behavior	Tg(Camk2a-tTA)1Mmay/0,Tg(tetO-Comt)1Kndl/0	involves: 129S6/SvEvTac * C57BL/6J	N	24639487
MGI:5694075	M	MP:0001468	abnormal temporal memory	Tg(Camk2a-tTA)1Mmay/0,Tg(tetO-Comt)1Kndl/0	involves: 129S6/SvEvTac * C57BL/6J	N	24639487
MGI:5694075	M	MP:0002062	abnormal associative learning	Tg(Camk2a-tTA)1Mmay/0,Tg(tetO-Comt)1Kndl/0	involves: 129S6/SvEvTac * C57BL/6J	N	24639487
MGI:5694075	M	MP:0010698	abnormal impulsive behavior control	Tg(Camk2a-tTA)1Mmay/0,Tg(tetO-Comt)1Kndl/0	involves: 129S6/SvEvTac * C57BL/6J	N	24639487
MGI:5694075	M	MP:0010149	abnormal synaptic dopamine release	Tg(Camk2a-tTA)1Mmay/0,Tg(tetO-Comt)1Kndl/0	involves: 129S6/SvEvTac * C57BL/6J	N	24639487
MGI:5694094	F	MP:0011894	decreased circulating transferrin level	Enam<Abte2>/Enam<+>	C3HeB/FeJ-Enam<Abte2>	N	22813216
MGI:5694094	F	MP:0001258	decreased body length	Enam<Abte2>/Enam<+>	C3HeB/FeJ-Enam<Abte2>	N	22813216
MGI:5694671	M	MP:0011585	decreased alkaline phosphatase activity	Gsdma3<Mhdaclp1>/Gsdma3<+>	C3HeB/FeJ-Gsdma3<Mhdaclp1>	N	22682752
MGI:5694718	F	MP:0005389	reproductive system phenotype	Wdr13<tm1Kuma>/Wdr13<tm1Kuma>	involves: 129S1/Sv * 129X1/SvJ * CD-1	Y	22715406
MGI:5694718	F	MP:0009285	increased gonadal fat pad weight	Wdr13<tm1Kuma>/Wdr13<tm1Kuma>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694718	F	MP:0009108	increased pancreas weight	Wdr13<tm1Kuma>/Wdr13<tm1Kuma>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694718	F	MP:0001260	increased body weight	Wdr13<tm1Kuma>/Wdr13<tm1Kuma>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694718	F	MP:0009118	increased white fat cell size	Wdr13<tm1Kuma>/Wdr13<tm1Kuma>	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694719	M	MP:0009108	increased pancreas weight	Wdr13<tm1Kuma>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694719	M	MP:0005292	improved glucose tolerance	Wdr13<tm1Kuma>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694719	M	MP:0002079	increased circulating insulin level	Wdr13<tm1Kuma>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694719	M	MP:0005658	increased susceptibility to diet-induced obesity	Wdr13<tm1Kuma>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694719	M	MP:0005389	reproductive system phenotype	Wdr13<tm1Kuma>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	Y	22715406
MGI:5694719	M	MP:0011819	increased pancreatic beta cell proliferation	Wdr13<tm1Kuma>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694719	M	MP:0005386	behavior/neurological phenotype	Wdr13<tm1Kuma>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	Y	22715406
MGI:5694719	M	MP:0005491	pancreatic islet hyperplasia	Wdr13<tm1Kuma>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694719	M	MP:0001260	increased body weight	Wdr13<tm1Kuma>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694719	M	MP:0009288	increased epididymal fat pad weight	Wdr13<tm1Kuma>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694719	M	MP:0005376	homeostasis/metabolism phenotype	Wdr13<tm1Kuma>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	Y	22715406
MGI:5694719	M	MP:0009118	increased white fat cell size	Wdr13<tm1Kuma>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694719	M	MP:0005560	decreased circulating glucose level	Wdr13<tm1Kuma>/Y	involves: 129S1/Sv * 129X1/SvJ * CD-1	N	22715406
MGI:5694815	M	MP:0005389	reproductive system phenotype	Lmtk3<tm1Tya>/Lmtk3<tm1Tya>	B6JJcl.Cg-Lmtk3<tm1Tya>	Y	24760852
MGI:5694992	F	MP:0010378	increased respiratory quotient	Npy1r<tm1Snby>/Npy1r<tm1Snby>,Npy5r<tm1Snby>/Npy5r<tm1Snby>	involves: 129 * C57BL/6	N	22768253
MGI:5694992	M	MP:0005293	impaired glucose tolerance	Npy1r<tm1Snby>/Npy1r<tm1Snby>,Npy5r<tm1Snby>/Npy5r<tm1Snby>	involves: 129 * C57BL/6	N	22768253
MGI:5694992	F	MP:0005559	increased circulating glucose level	Npy1r<tm1Snby>/Npy1r<tm1Snby>,Npy5r<tm1Snby>/Npy5r<tm1Snby>	involves: 129 * C57BL/6	N	22768253
MGI:5694992	M	MP:0010182	decreased susceptibility to weight gain	Npy1r<tm1Snby>/Npy1r<tm1Snby>,Npy5r<tm1Snby>/Npy5r<tm1Snby>	involves: 129 * C57BL/6	N	22768253
MGI:5694992	M	MP:0010024	increased total body fat amount	Npy1r<tm1Snby>/Npy1r<tm1Snby>,Npy5r<tm1Snby>/Npy5r<tm1Snby>	involves: 129 * C57BL/6	N	22768253
MGI:5694992	M	MP:0000008	increased white adipose tissue amount	Npy1r<tm1Snby>/Npy1r<tm1Snby>,Npy5r<tm1Snby>/Npy5r<tm1Snby>	involves: 129 * C57BL/6	N	22768253
MGI:5694992	M	MP:0004889	increased energy expenditure	Npy1r<tm1Snby>/Npy1r<tm1Snby>,Npy5r<tm1Snby>/Npy5r<tm1Snby>	involves: 129 * C57BL/6	N	22768253
MGI:5694992	F	MP:0010379	decreased respiratory quotient	Npy1r<tm1Snby>/Npy1r<tm1Snby>,Npy5r<tm1Snby>/Npy5r<tm1Snby>	involves: 129 * C57BL/6	N	22768253
MGI:5694993	F	MP:0004889	increased energy expenditure	Del(8Npy5r-Npy1r)1Snby/Del(8Npy5r-Npy1r)1Snby	involves: 129 * C57BL/6	N	22768253
MGI:5694993	M	MP:0011940	decreased food intake	Del(8Npy5r-Npy1r)1Snby/Del(8Npy5r-Npy1r)1Snby	involves: 129 * C57BL/6	N	22768253
MGI:5694993	F	MP:0001399	hyperactivity	Del(8Npy5r-Npy1r)1Snby/Del(8Npy5r-Npy1r)1Snby	involves: 129 * C57BL/6	N	22768253
MGI:5694993	M	MP:0001260	increased body weight	Del(8Npy5r-Npy1r)1Snby/Del(8Npy5r-Npy1r)1Snby	involves: 129 * C57BL/6	N	22768253
MGI:5694993	F	MP:0003961	decreased lean body mass	Del(8Npy5r-Npy1r)1Snby/Del(8Npy5r-Npy1r)1Snby	involves: 129 * C57BL/6	N	22768253
MGI:5694993	M	MP:0004890	decreased energy expenditure	Del(8Npy5r-Npy1r)1Snby/Del(8Npy5r-Npy1r)1Snby	involves: 129 * C57BL/6	N	22768253
MGI:5695082	M	MP:0004851	increased testis weight	Safb2<tm1So>/Safb2<tm1So>	involves: 129/Sv * C57BL/6J	N	26092125
MGI:5695082	M	MP:0002776	increased Sertoli cell number	Safb2<tm1So>/Safb2<tm1So>	involves: 129/Sv * C57BL/6J	N	26092125
MGI:5695334	M	MP:0002686	globozoospermia	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	M	MP:0008898	abnormal acrosome morphology	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	F	MP:0005389	reproductive system phenotype	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	Y	23459139
MGI:5695334	M	MP:0009838	abnormal sperm axoneme morphology	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	M	MP:0000599	enlarged liver	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	M	MP:0000607	abnormal hepatocyte morphology	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	M	MP:0000603	pale liver	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	M	MP:0002941	increased circulating alanine transaminase level	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	M	MP:0005343	increased circulating aspartate transaminase level	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	M	MP:0012216	decreased plasmalogen level	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	M	MP:0011971	increased circulating lactate dehydrogenase level	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	M	MP:0001402	decreased locomotor activity	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	M	MP:0002628	hepatic steatosis	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	M	MP:0009647	decreased fertilization frequency	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695334	M	MP:0001925	male infertility	Tysnd1<tm1.1Arte>/Tysnd1<tm1.1Arte>	involves: C57BL/6J * C57BL/6N	N	23459139
MGI:5695367	F	MP:0008083	decreased single-positive T cell number	Rasgrp1<tm1.1Wz>/Rasgrp1<tm1.1Wz>,Tg(TcraH-Y,TcrbH-Y)71Vbo/?	involves: C57BL/6J * DBA/2J	N	22719950
MGI:5695367	M	MP:0005091	increased double-positive T cell number	Rasgrp1<tm1.1Wz>/Rasgrp1<tm1.1Wz>,Tg(TcraH-Y,TcrbH-Y)71Vbo/?	involves: C57BL/6J * DBA/2J	N	22719950
MGI:5695532	M	MP:0008261	arrest of male meiosis	Lmna<tm1Rben>/Lmna<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ	N	23382700
MGI:5695532	M	MP:0001925	male infertility	Lmna<tm1Rben>/Lmna<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ	N	23382700
MGI:5695532	F	MP:0005168	abnormal female meiosis	Lmna<tm1Rben>/Lmna<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ	N	23382700
MGI:5695532	M	MP:0001147	small testis	Lmna<tm1Rben>/Lmna<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ	N	23382700
MGI:5695532	F	MP:0005389	reproductive system phenotype	Lmna<tm1Rben>/Lmna<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ	Y	23382700
MGI:5695532	M	MP:0005159	azoospermia	Lmna<tm1Rben>/Lmna<tm1Rben>	involves: 129S1/Sv * 129X1/SvJ	N	23382700
MGI:5695663	M	MP:0003186	abnormal redox activity	Nox4<tm1Syb>/Nox4<tm1Syb>	involves: 129S4/SvJae * C57BL/6N	N	23749776
MGI:5696127	F	MP:0005014	increased B cell number	Anxa5<tm1Epo>/Anxa5<tm1Epo>,Anxa6<tm1Moss>/Anxa6<tm1Moss>	involves: 129P2/OlaHsd * C57BL/6	N	22692895
MGI:5696127	F	MP:0008127	decreased dendritic cell number	Anxa5<tm1Epo>/Anxa5<tm1Epo>,Anxa6<tm1Moss>/Anxa6<tm1Moss>	involves: 129P2/OlaHsd * C57BL/6	N	22692895
MGI:5696128	F	MP:0003408	increased width of hypertrophic chondrocyte zone	Anxa5<tm1Epo>/Anxa5<tm1Epo>,Anxa6<tm1Moss>/Anxa6<tm1Moss>,Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	22692895
MGI:5696128	F	MP:0013763	increased T-helper cell number	Anxa5<tm1Epo>/Anxa5<tm1Epo>,Anxa6<tm1Moss>/Anxa6<tm1Moss>,Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	22692895
MGI:5696128	F	MP:0008127	decreased dendritic cell number	Anxa5<tm1Epo>/Anxa5<tm1Epo>,Anxa6<tm1Moss>/Anxa6<tm1Moss>,Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	22692895
MGI:5696128	F	MP:0005014	increased B cell number	Anxa5<tm1Epo>/Anxa5<tm1Epo>,Anxa6<tm1Moss>/Anxa6<tm1Moss>,Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	22692895
MGI:5696128	F	MP:0000559	abnormal femur morphology	Anxa5<tm1Epo>/Anxa5<tm1Epo>,Anxa6<tm1Moss>/Anxa6<tm1Moss>,Col10a1<tm1Ksec>/Col10a1<tm1Ksec>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	22692895
MGI:5696613	F	MP:0005366	variegated coat color	Atp7a<Mo-dp>/Atp7a<+>	involves: 101/H * C3H/HeH	N	25456742
MGI:5696613	F	MP:0011215	decreased brain copper level	Atp7a<Mo-dp>/Atp7a<+>	involves: 101/H * C3H/HeH	N	25456742
MGI:5696613	F	MP:0001274	curly vibrissae	Atp7a<Mo-dp>/Atp7a<+>	involves: 101/H * C3H/HeH	N	25456742
MGI:5696613	F	MP:0005584	abnormal enzyme/coenzyme activity	Atp7a<Mo-dp>/Atp7a<+>	involves: 101/H * C3H/HeH	N	25456742
MGI:5696613	F	MP:0012574	decreased noradrenaline level	Atp7a<Mo-dp>/Atp7a<+>	involves: 101/H * C3H/HeH	N	25456742
MGI:5696618	M	MP:0005289	increased oxygen consumption	Lepr<tm5Mgmj>/Lepr<tm5Mgmj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	24024119
MGI:5696618	F	MP:0005669	increased circulating leptin level	Lepr<tm5Mgmj>/Lepr<tm5Mgmj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	24024119
MGI:5696618	F	MP:0005389	reproductive system phenotype	Lepr<tm5Mgmj>/Lepr<tm5Mgmj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	24024119
MGI:5696618	F	MP:0031419	delayed estrus	Lepr<tm5Mgmj>/Lepr<tm5Mgmj>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	24024119
MGI:5696621	M	MP:0006208	lethality throughout fetal growth and development	Atp7a<Mo-dp>/Y	involves: 101/H * C3H/HeH	N	25456742
MGI:5696742	F	MP:0005124	increased circulating prolactin level	Tg(Prl-EGFR)#Sme/0	Not Specified	N	25375038
MGI:5696742	F	MP:0003505	increased prolactinoma incidence	Tg(Prl-EGFR)#Sme/0	Not Specified	N	25375038
MGI:5696778	M	MP:0001922	reduced male fertility	Usp19<Gt(XG128)Byg>/Usp19<Gt(XG128)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	26048142
MGI:5696781	F	MP:0001935	decreased litter size	Hmmr<tm1Plou>/Hmmr<tm1Plou>	involves: C57BL/6 * C57BL/6J	N	25750434
MGI:5696781	F	MP:0009761	abnormal meiotic spindle morphology	Hmmr<tm1Plou>/Hmmr<tm1Plou>	involves: C57BL/6 * C57BL/6J	N	25750434
MGI:5696781	F	MP:0008868	abnormal granulosa cell morphology	Hmmr<tm1Plou>/Hmmr<tm1Plou>	involves: C57BL/6 * C57BL/6J	N	25750434
MGI:5696781	F	MP:0001923	reduced female fertility	Hmmr<tm1Plou>/Hmmr<tm1Plou>	involves: C57BL/6 * C57BL/6J	N	25750434
MGI:5696781	F	MP:0002682	decreased mature ovarian follicle number	Hmmr<tm1Plou>/Hmmr<tm1Plou>	involves: C57BL/6 * C57BL/6J	N	25750434
MGI:5696781	F	MP:0031381	decreased secondary ovarian follicle number	Hmmr<tm1Plou>/Hmmr<tm1Plou>	involves: C57BL/6 * C57BL/6J	N	25750434
MGI:5696781	F	MP:0001129	impaired ovarian folliculogenesis	Hmmr<tm1Plou>/Hmmr<tm1Plou>	involves: C57BL/6 * C57BL/6J	N	25750434
MGI:5696781	F	MP:0011129	decreased tertiary ovarian follicle number	Hmmr<tm1Plou>/Hmmr<tm1Plou>	involves: C57BL/6 * C57BL/6J	N	25750434
MGI:5696781	F	MP:0005431	decreased oocyte number	Hmmr<tm1Plou>/Hmmr<tm1Plou>	involves: C57BL/6 * C57BL/6J	N	25750434
MGI:5696781	F	MP:0005389	reproductive system phenotype	Hmmr<tm1Plou>/Hmmr<tm1Plou>	involves: C57BL/6 * C57BL/6J	Y	25750434
MGI:5696781	F	MP:0011125	decreased primary ovarian follicle number	Hmmr<tm1Plou>/Hmmr<tm1Plou>	involves: C57BL/6 * C57BL/6J	N	25750434
MGI:5697155	M	MP:0010948	abnormal double-strand DNA break repair	Setx<tm1.1Mfl>/Setx<tm1.1Mfl>	Not Specified	N	23593030
MGI:5697155	M	MP:0005169	abnormal male meiosis	Setx<tm1.1Mfl>/Setx<tm1.1Mfl>	Not Specified	N	23593030
MGI:5697155	M	MP:0001932	abnormal spermiogenesis	Setx<tm1.1Mfl>/Setx<tm1.1Mfl>	Not Specified	N	23593030
MGI:5697155	M	MP:0014052	increased male germ cell apoptosis	Setx<tm1.1Mfl>/Setx<tm1.1Mfl>	Not Specified	N	23593030
MGI:5697155	M	MP:0001147	small testis	Setx<tm1.1Mfl>/Setx<tm1.1Mfl>	Not Specified	N	23593030
MGI:5697155	M	MP:0002686	globozoospermia	Setx<tm1.1Mfl>/Setx<tm1.1Mfl>	Not Specified	N	23593030
MGI:5697155	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Setx<tm1.1Mfl>/Setx<tm1.1Mfl>	Not Specified	N	23593030
MGI:5697155	M	MP:0005159	azoospermia	Setx<tm1.1Mfl>/Setx<tm1.1Mfl>	Not Specified	N	23593030
MGI:5697155	M	MP:0002216	abnormal seminiferous tubule morphology	Setx<tm1.1Mfl>/Setx<tm1.1Mfl>	Not Specified	N	23593030
MGI:5697155	M	MP:0008261	arrest of male meiosis	Setx<tm1.1Mfl>/Setx<tm1.1Mfl>	Not Specified	N	23593030
MGI:5697155	F	MP:0001923	reduced female fertility	Setx<tm1.1Mfl>/Setx<tm1.1Mfl>	Not Specified	N	23593030
MGI:5697155	M	MP:0001925	male infertility	Setx<tm1.1Mfl>/Setx<tm1.1Mfl>	Not Specified	N	23593030
MGI:5697335	F	MP:0001775	abnormal selenium level	Lrp2<tm1Her>/Lrp2<tm1Her>	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	24434121
MGI:5697652	M	MP:0003084	abnormal skeletal muscle fiber morphology	Dmd<mdx>/Dmd<mdx>	D2.B10-Dmd<mdx>/J	N	26566673
MGI:5697656	M	MP:0009745	abnormal behavioral response to xenobiotic	Trpm2<tm1Yamo>/Trpm2<tm1Yamo>	B6J.129S4-Trpm2<tm1Yamo>	N	26311765
MGI:5697656	M	MP:0001363	increased anxiety-related response	Trpm2<tm1Yamo>/Trpm2<tm1Yamo>	B6J.129S4-Trpm2<tm1Yamo>	N	26311765
MGI:5697656	M	MP:0001360	abnormal social investigation	Trpm2<tm1Yamo>/Trpm2<tm1Yamo>	B6J.129S4-Trpm2<tm1Yamo>	N	26311765
MGI:5697656	M	MP:0004994	abnormal brain wave pattern	Trpm2<tm1Yamo>/Trpm2<tm1Yamo>	B6J.129S4-Trpm2<tm1Yamo>	N	26311765
MGI:5697928	M	MP:0005459	decreased percent body fat/body weight	Dbx1<tm2Jcor>/Dbx1<tm1Tmj>,Tg(Nkx2-1-cre)2Sand/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	25864637
MGI:5697928	F	MP:0003462	abnormal response to novel odor	Dbx1<tm2Jcor>/Dbx1<tm1Tmj>,Tg(Nkx2-1-cre)2Sand/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	25864637
MGI:5697928	F	MP:0011957	decreased compensatory feeding amount	Dbx1<tm2Jcor>/Dbx1<tm1Tmj>,Tg(Nkx2-1-cre)2Sand/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	25864637
MGI:5697928	F	MP:0001752	abnormal hypothalamus secretion	Dbx1<tm2Jcor>/Dbx1<tm1Tmj>,Tg(Nkx2-1-cre)2Sand/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	25864637
MGI:5697928	F	MP:0011940	decreased food intake	Dbx1<tm2Jcor>/Dbx1<tm1Tmj>,Tg(Nkx2-1-cre)2Sand/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	25864637
MGI:5697928	M	MP:0031391	increased locomotor activity	Dbx1<tm2Jcor>/Dbx1<tm1Tmj>,Tg(Nkx2-1-cre)2Sand/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	25864637
MGI:5698146	M	MP:0030332	accelerated temporomandibular joint osteoarthritis	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	16612079
MGI:5698146	M	MP:0014101	decreased chondrocyte proliferation	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	16006154
MGI:5698146	M	MP:0000458	abnormal mandible morphology	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	16612079
MGI:5698146	M	MP:0013304	osteophytes	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	16006154
MGI:5698146	M	MP:0030332	accelerated temporomandibular joint osteoarthritis	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	16006154
MGI:5698146	M	MP:0006042	increased apoptosis	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	16612079
MGI:5698146	M	MP:0006433	abnormal articular cartilage morphology	Bgn<tm1Mfy>/Y,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	16006154
MGI:5698147	F	MP:0030332	accelerated temporomandibular joint osteoarthritis	Bgn<tm1Mfy>/Bgn<tm1Mfy>,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	16006154
MGI:5698147	F	MP:0014101	decreased chondrocyte proliferation	Bgn<tm1Mfy>/Bgn<tm1Mfy>,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	16006154
MGI:5698147	F	MP:0006433	abnormal articular cartilage morphology	Bgn<tm1Mfy>/Bgn<tm1Mfy>,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	16006154
MGI:5698147	F	MP:0013304	osteophytes	Bgn<tm1Mfy>/Bgn<tm1Mfy>,Fmod<tm1Aol>/Fmod<tm1Aol>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	16006154
MGI:5698212	M	MP:0004852	decreased testis weight	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0005159	azoospermia	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22571926
MGI:5698212	M	MP:0005159	azoospermia	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0001156	abnormal spermatogenesis	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22571926
MGI:5698212	M	MP:0014052	increased male germ cell apoptosis	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22571926
MGI:5698212	M	MP:0001925	male infertility	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22571926
MGI:5698212	M	MP:0001925	male infertility	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0005418	abnormal circulating hormone level	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0001776	abnormal circulating sodium level	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0011178	increased erythroblast number	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0004956	decreased thymus weight	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0005459	decreased percent body fat/body weight	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0009176	increased pancreatic alpha cell number	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0002776	increased Sertoli cell number	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0001155	arrest of spermatogenesis	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22571926
MGI:5698212	M	MP:0001262	decreased body weight	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0002079	increased circulating insulin level	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22571926
MGI:5698212	M	MP:0002781	increased circulating testosterone level	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0010135	increased DN4 thymocyte number	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0010134	decreased DN3 thymocyte number	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0001152	increased Leydig cell number	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0001750	increased circulating follicle stimulating hormone level	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0002078	abnormal glucose homeostasis	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0001765	abnormal ion homeostasis	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0002665	decreased circulating corticosterone level	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0005666	abnormal adipose tissue physiology	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0008261	arrest of male meiosis	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22571926
MGI:5698212	M	MP:0008827	abnormal thymus cell ratio	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0005627	increased circulating potassium level	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22556341
MGI:5698212	M	MP:0004852	decreased testis weight	Tsc22d3<tm1.2Hum>/Y	involves: 129S1/SvImJ	N	22571926
MGI:5698236	F	MP:0005389	reproductive system phenotype	Tsc22d3<tm1.2Hum>/Tsc22d3<+>	involves: 129S1/SvImJ	Y	22556341
MGI:5698247	M	MP:0005665	increased circulating noradrenaline level	Acvrl1<tm1Enl>/Acvrl1<+>	B6.Cg-Acvrl1<tm1Enl>	N	26398936
MGI:5698247	M	MP:0011022	abnormal circadian regulation of systemic arterial blood pressure	Acvrl1<tm1Enl>/Acvrl1<+>	B6.Cg-Acvrl1<tm1Enl>	N	26398936
MGI:5698247	M	MP:0004183	abnormal sympathetic nervous system physiology	Acvrl1<tm1Enl>/Acvrl1<+>	B6.Cg-Acvrl1<tm1Enl>	N	26398936
MGI:5698247	M	MP:0000231	hypertension	Acvrl1<tm1Enl>/Acvrl1<+>	B6.Cg-Acvrl1<tm1Enl>	N	26398936
MGI:5698247	M	MP:0001038	abnormal cholinergic neuron morphology	Acvrl1<tm1Enl>/Acvrl1<+>	B6.Cg-Acvrl1<tm1Enl>	N	26398936
MGI:5698247	M	MP:0031231	decreased circulating angiotensin II level	Acvrl1<tm1Enl>/Acvrl1<+>	B6.Cg-Acvrl1<tm1Enl>	N	26398936
MGI:5698247	M	MP:0008872	abnormal physiological response to xenobiotic	Acvrl1<tm1Enl>/Acvrl1<+>	B6.Cg-Acvrl1<tm1Enl>	N	26398936
MGI:5698247	M	MP:0012676	dilated brain ventricle	Acvrl1<tm1Enl>/Acvrl1<+>	B6.Cg-Acvrl1<tm1Enl>	N	26398936
MGI:5698247	M	MP:0005662	increased circulating adrenaline level	Acvrl1<tm1Enl>/Acvrl1<+>	B6.Cg-Acvrl1<tm1Enl>	N	26398936
MGI:5698247	M	MP:0005367	renal/urinary system phenotype	Acvrl1<tm1Enl>/Acvrl1<+>	B6.Cg-Acvrl1<tm1Enl>	Y	26398936
MGI:5698247	M	MP:0005584	abnormal enzyme/coenzyme activity	Acvrl1<tm1Enl>/Acvrl1<+>	B6.Cg-Acvrl1<tm1Enl>	N	26398936
MGI:5698359	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-DMTF1_i2)7Kai/0	FVB/NJ-Tg(MMTV-DMTF1_i2)7Kai	N	25537728
MGI:5698359	F	MP:0000630	mammary gland hyperplasia	Tg(MMTV-DMTF1_i2)7Kai/0	FVB/NJ-Tg(MMTV-DMTF1_i2)7Kai	N	25537728
MGI:5698410	M	MP:0030978	impaired binding of sperm to zona pellucida	Ly6k<tm1Osb>/Ly6k<tm1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	24501175
MGI:5698410	M	MP:0031012	impaired sperm migration in female genital tract	Ly6k<tm1Osb>/Ly6k<tm1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	24501175
MGI:5698410	M	MP:0001925	male infertility	Ly6k<tm1Osb>/Ly6k<tm1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	24501175
MGI:5698523	M	MP:0013438	dysmyelination	Htt<tm2Detl>/Htt<+>	B6J.129P2-Htt<tm2Detl>	N	25609071
MGI:5698523	M	MP:0001263	weight loss	Htt<tm2Detl>/Htt<+>	B6J.129P2-Htt<tm2Detl>	N	25609071
MGI:5698523	M	MP:0008918	microgliosis	Htt<tm2Detl>/Htt<+>	B6J.129P2-Htt<tm2Detl>	N	25609071
MGI:5698523	M	MP:0030635	increased taurine level	Htt<tm2Detl>/Htt<+>	B6J.129P2-Htt<tm2Detl>	N	25609071
MGI:5698523	M	MP:0004191	neuronal intranuclear inclusions	Htt<tm2Detl>/Htt<+>	B6J.129P2-Htt<tm2Detl>	N	25609071
MGI:5698523	M	MP:0001405	impaired coordination	Htt<tm2Detl>/Htt<+>	B6J.129P2-Htt<tm2Detl>	N	25609071
MGI:5698523	M	MP:0011731	decreased myelin sheath thickness	Htt<tm2Detl>/Htt<+>	B6J.129P2-Htt<tm2Detl>	N	25609071
MGI:5698523	M	MP:0012506	brain atrophy	Htt<tm2Detl>/Htt<+>	B6J.129P2-Htt<tm2Detl>	N	25609071
MGI:5698523	M	MP:0004077	abnormal striatum morphology	Htt<tm2Detl>/Htt<+>	B6J.129P2-Htt<tm2Detl>	N	25609071
MGI:5698523	M	MP:0009808	decreased oligodendrocyte number	Htt<tm2Detl>/Htt<+>	B6J.129P2-Htt<tm2Detl>	N	25609071
MGI:5698523	M	MP:0008917	abnormal oligodendrocyte physiology	Htt<tm2Detl>/Htt<+>	B6J.129P2-Htt<tm2Detl>	N	25609071
MGI:5698523	M	MP:0000920	abnormal myelination	Htt<tm2Detl>/Htt<+>	B6J.129P2-Htt<tm2Detl>	N	25609071
MGI:5698523	M	MP:0020070	decreased neocortex volume	Htt<tm2Detl>/Htt<+>	B6J.129P2-Htt<tm2Detl>	N	25609071
MGI:5698534	F	MP:0003997	tonic-clonic seizures	Syn1<tm1Pggd>/Syn1<tm1Pggd>,Syn2<tm1Pggd>/Syn2<tm1Pggd>,Syn3<tm1Pggd>/Syn3<tm1Pggd>	involves: 129 * 129P2/OlaHsd * 129X1/SvJ * C57BL/6	N	21621590
MGI:5698534	F	MP:0004994	abnormal brain wave pattern	Syn1<tm1Pggd>/Syn1<tm1Pggd>,Syn2<tm1Pggd>/Syn2<tm1Pggd>,Syn3<tm1Pggd>/Syn3<tm1Pggd>	involves: 129 * 129P2/OlaHsd * 129X1/SvJ * C57BL/6	N	21621590
MGI:5698534	F	MP:0009358	environmentally induced seizures	Syn1<tm1Pggd>/Syn1<tm1Pggd>,Syn2<tm1Pggd>/Syn2<tm1Pggd>,Syn3<tm1Pggd>/Syn3<tm1Pggd>	involves: 129 * 129P2/OlaHsd * 129X1/SvJ * C57BL/6	N	21621590
MGI:5698703	M	MP:0001147	small testis	Rab18<m1Hongc>/Rab18<m1Hongc>	C57BL/6J-Rab18<m1Hongc>	N	25779931
MGI:5699093	M	MP:0000747	muscle weakness	Tg(EIF1AX-Aldh2*E487K)101Oht/Tg(EIF1AX-Aldh2*E487K)101Oht	C57BL/6-Tg(EIF1AX-Aldh2*E487K)101Oht	N	18550766
MGI:5699093	F	MP:0012307	impaired spatial learning	Tg(EIF1AX-Aldh2*E487K)101Oht/Tg(EIF1AX-Aldh2*E487K)101Oht	C57BL/6-Tg(EIF1AX-Aldh2*E487K)101Oht	N	18550766
MGI:5699093	M	MP:0002075	abnormal coat/hair pigmentation	Tg(EIF1AX-Aldh2*E487K)101Oht/Tg(EIF1AX-Aldh2*E487K)101Oht	C57BL/6-Tg(EIF1AX-Aldh2*E487K)101Oht	N	18550766
MGI:5699093	M	MP:0001458	abnormal object recognition memory	Tg(EIF1AX-Aldh2*E487K)101Oht/Tg(EIF1AX-Aldh2*E487K)101Oht	C57BL/6-Tg(EIF1AX-Aldh2*E487K)101Oht	N	18550766
MGI:5699172	M	MP:0009455	enhanced cued conditioning behavior	Spire1<Gt(OST416113)Lex>/Spire1<Gt(OST416113)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	24345451
MGI:5699172	M	MP:0009453	enhanced contextual conditioning behavior	Spire1<Gt(OST416113)Lex>/Spire1<Gt(OST416113)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	24345451
MGI:5699361	M	MP:0009232	abnormal sperm nucleus morphology	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0002687	oligozoospermia	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0014052	increased male germ cell apoptosis	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0001146	abnormal testis morphology	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0004852	decreased testis weight	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0009239	short sperm flagellum	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0002631	abnormal epididymis morphology	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0005578	teratozoospermia	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0001156	abnormal spermatogenesis	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0009838	abnormal sperm axoneme morphology	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0001932	abnormal spermiogenesis	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0001153	small seminiferous tubules	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0009231	detached acrosome	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0009830	abnormal sperm connecting piece morphology	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0001925	male infertility	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0001929	abnormal gametogenesis	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699361	M	MP:0008892	abnormal sperm flagellum morphology	Cep131<Gt(CC0635)Wtsi>/Cep131<Gt(CC0635)Wtsi>	involves: 129P2/OlaHsd * C57BL/6	N	24415959
MGI:5699404	M	MP:0005293	impaired glucose tolerance	Afmid<tm1b(EUCOMM)Wtsi>/Afmid<+>	C57BL/6N-Afmid<tm1b(EUCOMM)Wtsi>/H	N	26432886
MGI:5699409	M	MP:0001559	hyperglycemia	Afmid<tm1a(EUCOMM)Wtsi>/Afmid<tm1a(EUCOMM)Wtsi>	C57BL/6N-Afmid<tm1a(EUCOMM)Wtsi>/H	N	26432886
MGI:5699558	M	MP:0003628	abnormal leukocyte adhesion	Glg1<Gt(RST092)Byg>/Glg1<+>	B6J.129P2-Glg1<Gt(RST092)Byg>	N	22939356
MGI:5699558	M	MP:0020333	enhanced leukocyte tethering or rolling	Glg1<Gt(RST092)Byg>/Glg1<+>	B6J.129P2-Glg1<Gt(RST092)Byg>	N	22939356
MGI:5700054	M	MP:0005627	increased circulating potassium level	Pou3f4<sdl>/Y	C3HeB/FeJ-Pou3f4<sdl>	N	23606368
MGI:5700054	M	MP:0001394	circling	Pou3f4<sdl>/Y	C3HeB/FeJ-Pou3f4<sdl>	N	23606368
MGI:5700054	M	MP:0006325	impaired hearing	Pou3f4<sdl>/Y	C3HeB/FeJ-Pou3f4<sdl>	N	23606368
MGI:5700054	M	MP:0005307	head tossing	Pou3f4<sdl>/Y	C3HeB/FeJ-Pou3f4<sdl>	N	23606368
MGI:5700078	M	MP:0005384	cellular phenotype	Topaz1<tm1Ics>/Topaz1<tm1Ics>	involves: C57BL/6J * C57BL/6N	Y	26358182
MGI:5700078	M	MP:0001147	small testis	Topaz1<tm1Ics>/Topaz1<tm1Ics>	involves: C57BL/6J * C57BL/6N	N	26358182
MGI:5700078	M	MP:0006362	abnormal male germ cell morphology	Topaz1<tm1Ics>/Topaz1<tm1Ics>	involves: C57BL/6J * C57BL/6N	N	26358182
MGI:5700078	M	MP:0004852	decreased testis weight	Topaz1<tm1Ics>/Topaz1<tm1Ics>	involves: C57BL/6J * C57BL/6N	N	26358182
MGI:5700078	F	MP:0005389	reproductive system phenotype	Topaz1<tm1Ics>/Topaz1<tm1Ics>	involves: C57BL/6J * C57BL/6N	Y	26358182
MGI:5700078	M	MP:0008280	abnormal male germ cell apoptosis	Topaz1<tm1Ics>/Topaz1<tm1Ics>	involves: C57BL/6J * C57BL/6N	N	26358182
MGI:5700078	M	MP:0005159	azoospermia	Topaz1<tm1Ics>/Topaz1<tm1Ics>	involves: C57BL/6J * C57BL/6N	N	26358182
MGI:5700078	M	MP:0008261	arrest of male meiosis	Topaz1<tm1Ics>/Topaz1<tm1Ics>	involves: C57BL/6J * C57BL/6N	N	26358182
MGI:5700078	M	MP:0001925	male infertility	Topaz1<tm1Ics>/Topaz1<tm1Ics>	involves: C57BL/6J * C57BL/6N	N	26358182
MGI:5700159	F	MP:0005389	reproductive system phenotype	Tsc22d3<tm1.2Hum>/Tsc22d3<tm1.2Hum>	involves: 129S1/SvImJ	Y	22571926
MGI:5700198	M	MP:0005389	reproductive system phenotype	Tsc22d3<tm1.1Hum>/Y,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/SvImJ * C57BL/6N * SJL/J	Y	22571926
MGI:5700201	M	MP:0001925	male infertility	Tsc22d3<tm1.1Hum>/Y,Tg(Ddx4-cre)1Dcas/0	involves: 129S1/SvImJ * C57BL/6N * FVB	N	22571926
MGI:5700201	M	MP:0001147	small testis	Tsc22d3<tm1.1Hum>/Y,Tg(Ddx4-cre)1Dcas/0	involves: 129S1/SvImJ * C57BL/6N * FVB	N	22571926
MGI:5700201	M	MP:0005159	azoospermia	Tsc22d3<tm1.1Hum>/Y,Tg(Ddx4-cre)1Dcas/0	involves: 129S1/SvImJ * C57BL/6N * FVB	N	22571926
MGI:5700201	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Tsc22d3<tm1.1Hum>/Y,Tg(Ddx4-cre)1Dcas/0	involves: 129S1/SvImJ * C57BL/6N * FVB	N	22571926
MGI:5700328	M	MP:0002628	hepatic steatosis	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	17906635
MGI:5700328	M	MP:0005292	improved glucose tolerance	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	17906635
MGI:5700328	M	MP:0000598	abnormal liver morphology	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	17906635
MGI:5700328	M	MP:0005280	abnormal fatty acids level	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	17906635
MGI:5700328	M	MP:0005378	growth/size/body region phenotype	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	involves: 129S5/SvEvBrd * C57BL/6	Y	17906635
MGI:5700328	M	MP:0002118	abnormal lipid homeostasis	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	17906635
MGI:5700328	M	MP:0003960	increased lean body mass	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	17906635
MGI:5700328	M	MP:0014172	decreased fatty acid oxidation	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	17906635
MGI:5700328	M	MP:0010080	abnormal hepatocyte physiology	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	17906635
MGI:5700328	M	MP:0002727	decreased circulating insulin level	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	17906635
MGI:5700328	M	MP:0005668	decreased circulating leptin level	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	17906635
MGI:5700328	M	MP:0005215	abnormal pancreatic islet morphology	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	17906635
MGI:5700328	M	MP:0002891	increased insulin sensitivity	Elovl6<Gt(OST222498)Lex>/Elovl6<Gt(OST222498)Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	17906635
MGI:5700792	F	MP:0005553	increased circulating creatinine level	Lrmda<tm1e(EUCOMM)Wtsi>/Lrmda<tm1e(EUCOMM)Wtsi>	C57BL/6N-1700112E06Rik<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700793	M	MP:0005293	impaired glucose tolerance	Pclaf<tm1a(EUCOMM)Wtsi>/Pclaf<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pclaf<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700798	F	MP:0004609	vertebral fusion	Abca4<tm1a(EUCOMM)Wtsi>/Abca4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Abca4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700799	F	MP:0002098	abnormal vibrissa morphology	Abcb6<tm1a(KOMP)Wtsi>/Abcb6<tm1a(KOMP)Wtsi>	C57BL/6N-Abcb6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700800	M	MP:0005292	improved glucose tolerance	Abhd14a<tm2a(EUCOMM)Wtsi>/Abhd14a<tm2a(EUCOMM)Wtsi>	C57BL/6N-Abhd14a<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700801	M	MP:0005292	improved glucose tolerance	Abhd17a<tm1a(KOMP)Wtsi>/Abhd17a<tm1a(KOMP)Wtsi>	C57BL/6N-Abhd17a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700802	F	MP:0001552	increased circulating triglyceride level	Acot5<tm1a(KOMP)Wtsi>/Acot5<tm1a(KOMP)Wtsi>	C57BL/6N-Acot5<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700802	M	MP:0010067	increased red blood cell distribution width	Acot5<tm1a(KOMP)Wtsi>/Acot5<tm1a(KOMP)Wtsi>	C57BL/6N-Acot5<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700803	F	MP:0001258	decreased body length	Acsl4<tm1a(EUCOMM)Wtsi>/Acsl4<tm1a(EUCOMM)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Acsl4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700810	M	MP:0003960	increased lean body mass	Adpgk<tm2a(EUCOMM)Wtsi>/Adpgk<tm2a(EUCOMM)Wtsi>	C57BL/6N-Adpgk<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700810	M	MP:0010052	increased grip strength	Adpgk<tm2a(EUCOMM)Wtsi>/Adpgk<tm2a(EUCOMM)Wtsi>	C57BL/6N-Adpgk<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700810	M	MP:0010123	increased bone mineral content	Adpgk<tm2a(EUCOMM)Wtsi>/Adpgk<tm2a(EUCOMM)Wtsi>	C57BL/6N-Adpgk<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700810	M	MP:0010025	decreased total body fat amount	Adpgk<tm2a(EUCOMM)Wtsi>/Adpgk<tm2a(EUCOMM)Wtsi>	C57BL/6N-Adpgk<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700810	M	MP:0000062	increased bone mineral density	Adpgk<tm2a(EUCOMM)Wtsi>/Adpgk<tm2a(EUCOMM)Wtsi>	C57BL/6N-Adpgk<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700815	F	MP:0010067	increased red blood cell distribution width	Arhgef15<tm1.1(KOMP)Vlcg>/Arhgef15<tm1.1(KOMP)Vlcg>	C57BL/6N-Arhgef15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700815	M	MP:0011110	preweaning lethality, incomplete penetrance	Arhgef15<tm1.1(KOMP)Vlcg>/Arhgef15<tm1.1(KOMP)Vlcg>	C57BL/6N-Arhgef15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700815	M	MP:0001925	male infertility	Arhgef15<tm1.1(KOMP)Vlcg>/Arhgef15<tm1.1(KOMP)Vlcg>	C57BL/6N-Arhgef15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700815	M	MP:0003402	decreased liver weight	Arhgef15<tm1.1(KOMP)Vlcg>/Arhgef15<tm1.1(KOMP)Vlcg>	C57BL/6N-Arhgef15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700815	M	MP:0001891	hydrocephaly	Arhgef15<tm1.1(KOMP)Vlcg>/Arhgef15<tm1.1(KOMP)Vlcg>	C57BL/6N-Arhgef15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700815	M	MP:0002152	abnormal brain morphology	Arhgef15<tm1.1(KOMP)Vlcg>/Arhgef15<tm1.1(KOMP)Vlcg>	C57BL/6N-Arhgef15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700823	F	MP:0005343	increased circulating aspartate transaminase level	Atxn3<tm1a(KOMP)Wtsi>/Atxn3<tm1a(KOMP)Wtsi>	C57BL/6N-Atxn3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700823	M	MP:0010088	decreased circulating fructosamine level	Atxn3<tm1a(KOMP)Wtsi>/Atxn3<tm1a(KOMP)Wtsi>	C57BL/6N-Atxn3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700824	M	MP:0000538	abnormal urinary bladder morphology	AU021092<tm1b(KOMP)Wtsi>/AU021092<tm1b(KOMP)Wtsi>	C57BL/6N-AU021092<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700824	M	MP:0002135	abnormal kidney morphology	AU021092<tm1b(KOMP)Wtsi>/AU021092<tm1b(KOMP)Wtsi>	C57BL/6N-AU021092<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700824	M	MP:0002833	increased heart weight	AU021092<tm1b(KOMP)Wtsi>/AU021092<tm1b(KOMP)Wtsi>	C57BL/6N-AU021092<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700825	F	MP:0013025	increased Ly6C low monocyte number	Bach2<tm1a(EUCOMM)Wtsi>/Bach2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700825	F	MP:0013022	increased Ly6C high monocyte number	Bach2<tm1a(EUCOMM)Wtsi>/Bach2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700825	F	MP:0010124	decreased bone mineral content	Bach2<tm1a(EUCOMM)Wtsi>/Bach2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700825	F	MP:0005554	decreased circulating creatinine level	Bach2<tm1a(EUCOMM)Wtsi>/Bach2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700825	F	MP:0000063	decreased bone mineral density	Bach2<tm1a(EUCOMM)Wtsi>/Bach2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700825	F	MP:0000219	increased neutrophil cell number	Bach2<tm1a(EUCOMM)Wtsi>/Bach2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700825	F	MP:0005505	thrombocytosis	Bach2<tm1a(EUCOMM)Wtsi>/Bach2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700828	M	MP:0011110	preweaning lethality, incomplete penetrance	Bves<tm1.1(KOMP)Vlcg>/Bves<tm1.1(KOMP)Vlcg>	C57BL/6N-Bves<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700828	M	MP:0005292	improved glucose tolerance	Bves<tm1.1(KOMP)Vlcg>/Bves<tm1.1(KOMP)Vlcg>	C57BL/6N-Bves<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700828	M	MP:0010052	increased grip strength	Bves<tm1.1(KOMP)Vlcg>/Bves<tm1.1(KOMP)Vlcg>	C57BL/6N-Bves<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700828	M	MP:0003402	decreased liver weight	Bves<tm1.1(KOMP)Vlcg>/Bves<tm1.1(KOMP)Vlcg>	C57BL/6N-Bves<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700828	M	MP:0002060	abnormal skin morphology	Bves<tm1.1(KOMP)Vlcg>/Bves<tm1.1(KOMP)Vlcg>	C57BL/6N-Bves<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700834	M	MP:0005505	thrombocytosis	Cd55b<tm1a(KOMP)Wtsi>/Cd55b<tm1a(KOMP)Wtsi>	C57BL/6N-Cd55b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700834	F	MP:0005553	increased circulating creatinine level	Cd55b<tm1a(KOMP)Wtsi>/Cd55b<tm1a(KOMP)Wtsi>	C57BL/6N-Cd55b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700835	F	MP:0002968	increased circulating alkaline phosphatase level	Chd9<tm1a(EUCOMM)Wtsi>/Chd9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Chd9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700835	M	MP:0005419	decreased circulating serum albumin level	Chd9<tm1a(EUCOMM)Wtsi>/Chd9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Chd9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700837	F	MP:0002098	abnormal vibrissa morphology	Chst8<tm1b(KOMP)Mbp>/Chst8<tm1b(KOMP)Mbp>	C57BL/6N-Chst8<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5700837	M	MP:0020870	decreased thigmotaxis	Chst8<tm1b(KOMP)Mbp>/Chst8<tm1b(KOMP)Mbp>	C57BL/6N-Chst8<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5700837	M	MP:0002092	abnormal eye morphology	Chst8<tm1b(KOMP)Mbp>/Chst8<tm1b(KOMP)Mbp>	C57BL/6N-Chst8<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5700837	M	MP:0004924	abnormal behavior	Chst8<tm1b(KOMP)Mbp>/Chst8<tm1b(KOMP)Mbp>	C57BL/6N-Chst8<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5700837	F	MP:0002941	increased circulating alanine transaminase level	Chst8<tm1b(KOMP)Mbp>/Chst8<tm1b(KOMP)Mbp>	C57BL/6N-Chst8<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5700841	M	MP:0008810	increased circulating iron level	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	F	MP:0013022	increased Ly6C high monocyte number	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	F	MP:0008347	decreased gamma-delta T cell number	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	M	MP:0005560	decreased circulating glucose level	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	M	MP:0002968	increased circulating alkaline phosphatase level	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	M	MP:0003179	thrombocytopenia	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	M	MP:0001925	male infertility	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	F	MP:0000218	increased leukocyte cell number	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	F	MP:0001926	female infertility	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	F	MP:0003795	abnormal bone structure	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	F	MP:0005014	increased B cell number	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	M	MP:0010025	decreased total body fat amount	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	F	MP:0000745	tremors	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	M	MP:0002965	increased circulating serum albumin level	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	M	MP:0005343	increased circulating aspartate transaminase level	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	F	MP:0010088	decreased circulating fructosamine level	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	F	MP:0013025	increased Ly6C low monocyte number	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700841	F	MP:0001258	decreased body length	Clpp<tm1a(EUCOMM)Wtsi>/Clpp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clpp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700842	M	MP:0000689	abnormal spleen morphology	Clrn1<tm1.1(KOMP)Vlcg>/Clrn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Clrn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700842	F	MP:0002098	abnormal vibrissa morphology	Clrn1<tm1.1(KOMP)Vlcg>/Clrn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Clrn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700842	M	MP:0001175	abnormal lung morphology	Clrn1<tm1.1(KOMP)Vlcg>/Clrn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Clrn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700842	M	MP:0000598	abnormal liver morphology	Clrn1<tm1.1(KOMP)Vlcg>/Clrn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Clrn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700842	M	MP:0002135	abnormal kidney morphology	Clrn1<tm1.1(KOMP)Vlcg>/Clrn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Clrn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700842	M	MP:0002060	abnormal skin morphology	Clrn1<tm1.1(KOMP)Vlcg>/Clrn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Clrn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700855	F	MP:0002599	increased mean platelet volume	Cxcl17<tm1b(EUCOMM)Wtsi>/Cxcl17<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl17<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5700855	F	MP:0001120	abnormal uterus morphology	Cxcl17<tm1b(EUCOMM)Wtsi>/Cxcl17<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl17<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5700855	F	MP:0000266	abnormal heart morphology	Cxcl17<tm1b(EUCOMM)Wtsi>/Cxcl17<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl17<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5700855	F	MP:0000274	enlarged heart	Cxcl17<tm1b(EUCOMM)Wtsi>/Cxcl17<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl17<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5700855	M	MP:0002075	abnormal coat/hair pigmentation	Cxcl17<tm1b(EUCOMM)Wtsi>/Cxcl17<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl17<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5700855	F	MP:0004906	enlarged uterus	Cxcl17<tm1b(EUCOMM)Wtsi>/Cxcl17<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl17<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5700855	M	MP:0002135	abnormal kidney morphology	Cxcl17<tm1b(EUCOMM)Wtsi>/Cxcl17<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl17<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5700855	F	MP:0002941	increased circulating alanine transaminase level	Cxcl17<tm1b(EUCOMM)Wtsi>/Cxcl17<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl17<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5700855	M	MP:0002060	abnormal skin morphology	Cxcl17<tm1b(EUCOMM)Wtsi>/Cxcl17<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl17<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5700857	F	MP:0000218	increased leukocyte cell number	Cxcr2<tm1a(EUCOMM)Wtsi>/Cxcr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700857	F	MP:0005478	decreased circulating thyroxine level	Cxcr2<tm1a(EUCOMM)Wtsi>/Cxcr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700857	F	MP:0000194	increased circulating calcium level	Cxcr2<tm1a(EUCOMM)Wtsi>/Cxcr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700857	F	MP:0005505	thrombocytosis	Cxcr2<tm1a(EUCOMM)Wtsi>/Cxcr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700857	F	MP:0013157	increased KLRG1+ CD4 alpha-beta T cell number	Cxcr2<tm1a(EUCOMM)Wtsi>/Cxcr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700857	F	MP:0000219	increased neutrophil cell number	Cxcr2<tm1a(EUCOMM)Wtsi>/Cxcr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700857	F	MP:0005562	decreased mean corpuscular hemoglobin	Cxcr2<tm1a(EUCOMM)Wtsi>/Cxcr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700857	F	MP:0005419	decreased circulating serum albumin level	Cxcr2<tm1a(EUCOMM)Wtsi>/Cxcr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700857	F	MP:0013022	increased Ly6C high monocyte number	Cxcr2<tm1a(EUCOMM)Wtsi>/Cxcr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700857	F	MP:0010088	decreased circulating fructosamine level	Cxcr2<tm1a(EUCOMM)Wtsi>/Cxcr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700860	F	MP:0005565	increased blood urea nitrogen level	D7Ertd443e<tm2a(KOMP)Wtsi>/D7Ertd443e<tm2a(KOMP)Wtsi>	C57BL/6N-D7Ertd443e<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700860	M	MP:0002941	increased circulating alanine transaminase level	D7Ertd443e<tm2a(KOMP)Wtsi>/D7Ertd443e<tm2a(KOMP)Wtsi>	C57BL/6N-D7Ertd443e<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700860	F	MP:0005553	increased circulating creatinine level	D7Ertd443e<tm2a(KOMP)Wtsi>/D7Ertd443e<tm2a(KOMP)Wtsi>	C57BL/6N-D7Ertd443e<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700861	M	MP:0010123	increased bone mineral content	Dap<tm1a(KOMP)Mbp>/Dap<tm1a(KOMP)Mbp>	C57BL/6N-Dap<tm1a(KOMP)Mbp>/Wtsi	N	MGI:5576271
MGI:5700861	M	MP:0001554	increased circulating free fatty acids level	Dap<tm1a(KOMP)Mbp>/Dap<tm1a(KOMP)Mbp>	C57BL/6N-Dap<tm1a(KOMP)Mbp>/Wtsi	N	MGI:5576271
MGI:5700861	M	MP:0002833	increased heart weight	Dap<tm1a(KOMP)Mbp>/Dap<tm1a(KOMP)Mbp>	C57BL/6N-Dap<tm1a(KOMP)Mbp>/Wtsi	N	MGI:5576271
MGI:5700863	F	MP:0002875	decreased erythrocyte cell number	Dcaf11<tm1a(KOMP)Wtsi>/Dcaf11<tm1a(KOMP)Wtsi>	C57BL/6N-Dcaf11<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700864	M	MP:0002833	increased heart weight	Dcbld2<tm1a(KOMP)Wtsi>/Dcbld2<tm1a(KOMP)Wtsi>	C57BL/6N-Dcbld2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700864	M	MP:0010088	decreased circulating fructosamine level	Dcbld2<tm1a(KOMP)Wtsi>/Dcbld2<tm1a(KOMP)Wtsi>	C57BL/6N-Dcbld2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700864	M	MP:0001512	trunk curl	Dcbld2<tm1a(KOMP)Wtsi>/Dcbld2<tm1a(KOMP)Wtsi>	C57BL/6N-Dcbld2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700864	F	MP:0004794	increased anti-nuclear antigen antibody level	Dcbld2<tm1a(KOMP)Wtsi>/Dcbld2<tm1a(KOMP)Wtsi>	C57BL/6N-Dcbld2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700870	F	MP:0003036	vertebral transformation	Dph6<tm1a(KOMP)Wtsi>/Dph6<tm1a(KOMP)Wtsi>	C57BL/6N-Dph6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700870	M	MP:0005553	increased circulating creatinine level	Dph6<tm1a(KOMP)Wtsi>/Dph6<tm1a(KOMP)Wtsi>	C57BL/6N-Dph6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700870	F	MP:0002075	abnormal coat/hair pigmentation	Dph6<tm1a(KOMP)Wtsi>/Dph6<tm1a(KOMP)Wtsi>	C57BL/6N-Dph6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700870	M	MP:0010092	increased circulating magnesium level	Dph6<tm1a(KOMP)Wtsi>/Dph6<tm1a(KOMP)Wtsi>	C57BL/6N-Dph6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700870	M	MP:0001258	decreased body length	Dph6<tm1a(KOMP)Wtsi>/Dph6<tm1a(KOMP)Wtsi>	C57BL/6N-Dph6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700870	M	MP:0005565	increased blood urea nitrogen level	Dph6<tm1a(KOMP)Wtsi>/Dph6<tm1a(KOMP)Wtsi>	C57BL/6N-Dph6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700878	M	MP:0005560	decreased circulating glucose level	Enc1<tm1a(EUCOMM)Wtsi>/Enc1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Enc1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700878	M	MP:0000186	decreased circulating HDL cholesterol level	Enc1<tm1a(EUCOMM)Wtsi>/Enc1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Enc1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700878	M	MP:0005179	decreased circulating cholesterol level	Enc1<tm1a(EUCOMM)Wtsi>/Enc1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Enc1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700878	M	MP:0005344	increased circulating bilirubin level	Enc1<tm1a(EUCOMM)Wtsi>/Enc1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Enc1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700878	F	MP:0002968	increased circulating alkaline phosphatase level	Enc1<tm1a(EUCOMM)Wtsi>/Enc1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Enc1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700879	F	MP:0005561	increased mean corpuscular hemoglobin	Epn3<tm1b(KOMP)Wtsi>/Epn3<tm1b(KOMP)Wtsi>	C57BL/6N-Epn3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700882	M	MP:0013278	decreased fasting circulating glucose level	Evi5<tm1a(KOMP)Wtsi>/Evi5<tm1a(KOMP)Wtsi>	C57BL/6N-Evi5<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700886	M	MP:0005419	decreased circulating serum albumin level	Fbf1<tm1a(EUCOMM)Wtsi>/Fbf1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbf1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700886	F	MP:0013279	increased fasting circulating glucose level	Fbf1<tm1a(EUCOMM)Wtsi>/Fbf1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbf1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700886	F	MP:0010124	decreased bone mineral content	Fbf1<tm1a(EUCOMM)Wtsi>/Fbf1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbf1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700886	M	MP:0002079	increased circulating insulin level	Fbf1<tm1a(EUCOMM)Wtsi>/Fbf1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbf1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700886	M	MP:0005296	abnormal humerus morphology	Fbf1<tm1a(EUCOMM)Wtsi>/Fbf1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbf1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700886	M	MP:0005179	decreased circulating cholesterol level	Fbf1<tm1a(EUCOMM)Wtsi>/Fbf1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbf1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700886	M	MP:0000186	decreased circulating HDL cholesterol level	Fbf1<tm1a(EUCOMM)Wtsi>/Fbf1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbf1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700886	F	MP:0003961	decreased lean body mass	Fbf1<tm1a(EUCOMM)Wtsi>/Fbf1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbf1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700886	F	MP:0003795	abnormal bone structure	Fbf1<tm1a(EUCOMM)Wtsi>/Fbf1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbf1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700886	F	MP:0010024	increased total body fat amount	Fbf1<tm1a(EUCOMM)Wtsi>/Fbf1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbf1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700889	F	MP:0002591	decreased mean corpuscular volume	Fcer1g<tm1b(KOMP)Wtsi>/Fcer1g<tm1b(KOMP)Wtsi>	C57BL/6N-Fcer1g<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700889	F	MP:0005562	decreased mean corpuscular hemoglobin	Fcer1g<tm1b(KOMP)Wtsi>/Fcer1g<tm1b(KOMP)Wtsi>	C57BL/6N-Fcer1g<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700890	M	MP:0000266	abnormal heart morphology	Fcrla<tm1b(KOMP)Wtsi>/Fcrla<tm1b(KOMP)Wtsi>	C57BL/6N-Fcrla<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700890	F	MP:0000691	enlarged spleen	Fcrla<tm1b(KOMP)Wtsi>/Fcrla<tm1b(KOMP)Wtsi>	C57BL/6N-Fcrla<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700890	M	MP:0000274	enlarged heart	Fcrla<tm1b(KOMP)Wtsi>/Fcrla<tm1b(KOMP)Wtsi>	C57BL/6N-Fcrla<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700890	F	MP:0009709	hydrometra	Fcrla<tm1b(KOMP)Wtsi>/Fcrla<tm1b(KOMP)Wtsi>	C57BL/6N-Fcrla<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700890	F	MP:0000689	abnormal spleen morphology	Fcrla<tm1b(KOMP)Wtsi>/Fcrla<tm1b(KOMP)Wtsi>	C57BL/6N-Fcrla<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700890	F	MP:0004906	enlarged uterus	Fcrla<tm1b(KOMP)Wtsi>/Fcrla<tm1b(KOMP)Wtsi>	C57BL/6N-Fcrla<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700890	F	MP:0002075	abnormal coat/hair pigmentation	Fcrla<tm1b(KOMP)Wtsi>/Fcrla<tm1b(KOMP)Wtsi>	C57BL/6N-Fcrla<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700890	F	MP:0001120	abnormal uterus morphology	Fcrla<tm1b(KOMP)Wtsi>/Fcrla<tm1b(KOMP)Wtsi>	C57BL/6N-Fcrla<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700890	M	MP:0002135	abnormal kidney morphology	Fcrla<tm1b(KOMP)Wtsi>/Fcrla<tm1b(KOMP)Wtsi>	C57BL/6N-Fcrla<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700895	M	MP:0001697	abnormal embryo size	Fgfr1<tm1.1(KOMP)Vlcg>/Fgfr1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fgfr1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700895	M	MP:0003984	embryonic growth retardation	Fgfr1<tm1.1(KOMP)Vlcg>/Fgfr1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fgfr1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700896	F	MP:0008810	increased circulating iron level	Fnip2<tm1a(KOMP)Wtsi>/Fnip2<tm1a(KOMP)Wtsi>	C57BL/6N-Fnip2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700899	M	MP:0004931	enlarged epididymis	Gbgt1<tm1.1(KOMP)Vlcg>/Gbgt1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gbgt1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700899	M	MP:0001147	small testis	Gbgt1<tm1.1(KOMP)Vlcg>/Gbgt1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gbgt1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700899	M	MP:0002631	abnormal epididymis morphology	Gbgt1<tm1.1(KOMP)Vlcg>/Gbgt1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gbgt1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700899	M	MP:0001146	abnormal testis morphology	Gbgt1<tm1.1(KOMP)Vlcg>/Gbgt1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gbgt1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700900	M	MP:0002135	abnormal kidney morphology	Gdf10<tm2b(KOMP)Wtsi>/Gdf10<tm2b(KOMP)Wtsi>	C57BL/6N-Gdf10<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700900	F	MP:0001402	decreased locomotor activity	Gdf10<tm2b(KOMP)Wtsi>/Gdf10<tm2b(KOMP)Wtsi>	C57BL/6N-Gdf10<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700900	M	MP:0003068	enlarged kidney	Gdf10<tm2b(KOMP)Wtsi>/Gdf10<tm2b(KOMP)Wtsi>	C57BL/6N-Gdf10<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700900	F	MP:0005344	increased circulating bilirubin level	Gdf10<tm2b(KOMP)Wtsi>/Gdf10<tm2b(KOMP)Wtsi>	C57BL/6N-Gdf10<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700905	F	MP:0002875	decreased erythrocyte cell number	Gmds<tm1a(KOMP)Wtsi>/Gmds<tm1a(KOMP)Wtsi>	C57BL/6N-Gmds<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700905	F	MP:0000208	decreased hematocrit	Gmds<tm1a(KOMP)Wtsi>/Gmds<tm1a(KOMP)Wtsi>	C57BL/6N-Gmds<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700905	F	MP:0010052	increased grip strength	Gmds<tm1a(KOMP)Wtsi>/Gmds<tm1a(KOMP)Wtsi>	C57BL/6N-Gmds<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700905	F	MP:0002874	decreased hemoglobin content	Gmds<tm1a(KOMP)Wtsi>/Gmds<tm1a(KOMP)Wtsi>	C57BL/6N-Gmds<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700905	F	MP:0000438	abnormal cranium morphology	Gmds<tm1a(KOMP)Wtsi>/Gmds<tm1a(KOMP)Wtsi>	C57BL/6N-Gmds<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700905	F	MP:0008810	increased circulating iron level	Gmds<tm1a(KOMP)Wtsi>/Gmds<tm1a(KOMP)Wtsi>	C57BL/6N-Gmds<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700905	F	MP:0003795	abnormal bone structure	Gmds<tm1a(KOMP)Wtsi>/Gmds<tm1a(KOMP)Wtsi>	C57BL/6N-Gmds<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700907	M	MP:0004931	enlarged epididymis	Gpr65<tm1b(KOMP)Wtsi>/Gpr65<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr65<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700907	F	MP:0000274	enlarged heart	Gpr65<tm1b(KOMP)Wtsi>/Gpr65<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr65<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700907	F	MP:0000266	abnormal heart morphology	Gpr65<tm1b(KOMP)Wtsi>/Gpr65<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr65<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700907	F	MP:0003960	increased lean body mass	Gpr65<tm1b(KOMP)Wtsi>/Gpr65<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr65<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700907	M	MP:0002631	abnormal epididymis morphology	Gpr65<tm1b(KOMP)Wtsi>/Gpr65<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr65<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700907	F	MP:0010025	decreased total body fat amount	Gpr65<tm1b(KOMP)Wtsi>/Gpr65<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr65<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700908	M	MP:0000266	abnormal heart morphology	Gpsm1<tm2b(KOMP)Wtsi>/Gpsm1<tm2b(KOMP)Wtsi>	C57BL/6N-Gpsm1<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700908	M	MP:0002135	abnormal kidney morphology	Gpsm1<tm2b(KOMP)Wtsi>/Gpsm1<tm2b(KOMP)Wtsi>	C57BL/6N-Gpsm1<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700908	M	MP:0000274	enlarged heart	Gpsm1<tm2b(KOMP)Wtsi>/Gpsm1<tm2b(KOMP)Wtsi>	C57BL/6N-Gpsm1<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700908	F	MP:0002060	abnormal skin morphology	Gpsm1<tm2b(KOMP)Wtsi>/Gpsm1<tm2b(KOMP)Wtsi>	C57BL/6N-Gpsm1<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700909	M	MP:0001258	decreased body length	Gpx1<tm1.1(KOMP)Vlcg>/Gpx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700909	M	MP:0004931	enlarged epididymis	Gpx1<tm1.1(KOMP)Vlcg>/Gpx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700909	M	MP:0001147	small testis	Gpx1<tm1.1(KOMP)Vlcg>/Gpx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700909	M	MP:0002631	abnormal epididymis morphology	Gpx1<tm1.1(KOMP)Vlcg>/Gpx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700909	M	MP:0001146	abnormal testis morphology	Gpx1<tm1.1(KOMP)Vlcg>/Gpx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700911	M	MP:0004174	abnormal spine curvature	H2-Eb1<b-tm1a(KOMP)Wtsi>/H2-Eb1<b-tm1a(KOMP)Wtsi>	C57BL/6N-H2-Eb1<b-tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700912	M	MP:0002599	increased mean platelet volume	Hbs1l<tm1a(KOMP)Wtsi>/Hbs1l<tm1a(KOMP)Wtsi>	C57BL/6N-Hbs1l<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700912	F	MP:0002968	increased circulating alkaline phosphatase level	Hbs1l<tm1a(KOMP)Wtsi>/Hbs1l<tm1a(KOMP)Wtsi>	C57BL/6N-Hbs1l<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700912	F	MP:0008810	increased circulating iron level	Hbs1l<tm1a(KOMP)Wtsi>/Hbs1l<tm1a(KOMP)Wtsi>	C57BL/6N-Hbs1l<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700912	M	MP:0005561	increased mean corpuscular hemoglobin	Hbs1l<tm1a(KOMP)Wtsi>/Hbs1l<tm1a(KOMP)Wtsi>	C57BL/6N-Hbs1l<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700912	F	MP:0000438	abnormal cranium morphology	Hbs1l<tm1a(KOMP)Wtsi>/Hbs1l<tm1a(KOMP)Wtsi>	C57BL/6N-Hbs1l<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700912	M	MP:0000223	decreased monocyte cell number	Hbs1l<tm1a(KOMP)Wtsi>/Hbs1l<tm1a(KOMP)Wtsi>	C57BL/6N-Hbs1l<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700912	M	MP:0001925	male infertility	Hbs1l<tm1a(KOMP)Wtsi>/Hbs1l<tm1a(KOMP)Wtsi>	C57BL/6N-Hbs1l<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700912	F	MP:0001314	cornea opacity	Hbs1l<tm1a(KOMP)Wtsi>/Hbs1l<tm1a(KOMP)Wtsi>	C57BL/6N-Hbs1l<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700912	M	MP:0001554	increased circulating free fatty acids level	Hbs1l<tm1a(KOMP)Wtsi>/Hbs1l<tm1a(KOMP)Wtsi>	C57BL/6N-Hbs1l<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700912	M	MP:0001925	male infertility	Hbs1l<tm1a(KOMP)Wtsi>/Hbs1l<tm1a(KOMP)Wtsi>	C57BL/6N-Hbs1l<tm1a(KOMP)Wtsi>/Wtsi	N	30707697
MGI:5700912	F	MP:0003036	vertebral transformation	Hbs1l<tm1a(KOMP)Wtsi>/Hbs1l<tm1a(KOMP)Wtsi>	C57BL/6N-Hbs1l<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700913	M	MP:0005333	decreased heart rate	Hcrt<tm1.1(KOMP)Vlcg>/Hcrt<tm1.1(KOMP)Vlcg>	C57BL/6N-Hcrt<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700913	F	MP:0001402	decreased locomotor activity	Hcrt<tm1.1(KOMP)Vlcg>/Hcrt<tm1.1(KOMP)Vlcg>	C57BL/6N-Hcrt<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700913	F	MP:0005013	increased lymphocyte cell number	Hcrt<tm1.1(KOMP)Vlcg>/Hcrt<tm1.1(KOMP)Vlcg>	C57BL/6N-Hcrt<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700913	M	MP:0010506	prolonged RR interval	Hcrt<tm1.1(KOMP)Vlcg>/Hcrt<tm1.1(KOMP)Vlcg>	C57BL/6N-Hcrt<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700921	M	MP:0002833	increased heart weight	Izumo1r<tm2a(KOMP)Wtsi>/Izumo1r<tm2a(KOMP)Wtsi>	C57BL/6N-Izumo1r<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700921	M	MP:0010025	decreased total body fat amount	Izumo1r<tm2a(KOMP)Wtsi>/Izumo1r<tm2a(KOMP)Wtsi>	C57BL/6N-Izumo1r<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700921	F	MP:0001926	female infertility	Izumo1r<tm2a(KOMP)Wtsi>/Izumo1r<tm2a(KOMP)Wtsi>	C57BL/6N-Izumo1r<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700921	M	MP:0008805	decreased circulating amylase level	Izumo1r<tm2a(KOMP)Wtsi>/Izumo1r<tm2a(KOMP)Wtsi>	C57BL/6N-Izumo1r<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700921	M	MP:0003960	increased lean body mass	Izumo1r<tm2a(KOMP)Wtsi>/Izumo1r<tm2a(KOMP)Wtsi>	C57BL/6N-Izumo1r<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700928	M	MP:0005013	increased lymphocyte cell number	Lpin3<tm1b(KOMP)Wtsi>/Lpin3<tm1b(KOMP)Wtsi>	C57BL/6N-Lpin3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700928	M	MP:0005011	increased eosinophil cell number	Lpin3<tm1b(KOMP)Wtsi>/Lpin3<tm1b(KOMP)Wtsi>	C57BL/6N-Lpin3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700928	F	MP:0001529	abnormal vocalization	Lpin3<tm1b(KOMP)Wtsi>/Lpin3<tm1b(KOMP)Wtsi>	C57BL/6N-Lpin3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700928	M	MP:0000218	increased leukocyte cell number	Lpin3<tm1b(KOMP)Wtsi>/Lpin3<tm1b(KOMP)Wtsi>	C57BL/6N-Lpin3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700928	M	MP:0000220	increased monocyte cell number	Lpin3<tm1b(KOMP)Wtsi>/Lpin3<tm1b(KOMP)Wtsi>	C57BL/6N-Lpin3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700928	M	MP:0002606	increased basophil cell number	Lpin3<tm1b(KOMP)Wtsi>/Lpin3<tm1b(KOMP)Wtsi>	C57BL/6N-Lpin3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700928	M	MP:0000219	increased neutrophil cell number	Lpin3<tm1b(KOMP)Wtsi>/Lpin3<tm1b(KOMP)Wtsi>	C57BL/6N-Lpin3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700933	F	MP:0001120	abnormal uterus morphology	Map3k8<tm1b(KOMP)Wtsi>/Map3k8<tm1b(KOMP)Wtsi>	C57BL/6N-Map3k8<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700941	M	MP:0005419	decreased circulating serum albumin level	Nfkbil1<tm1a(KOMP)Wtsi>/Nfkbil1<tm1a(KOMP)Wtsi>	C57BL/6N-Nfkbil1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700954	M	MP:0010123	increased bone mineral content	Osbpl3<tm1a(EUCOMM)Wtsi>/Osbpl3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Osbpl3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700954	M	MP:0000062	increased bone mineral density	Osbpl3<tm1a(EUCOMM)Wtsi>/Osbpl3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Osbpl3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700954	M	MP:0003960	increased lean body mass	Osbpl3<tm1a(EUCOMM)Wtsi>/Osbpl3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Osbpl3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700954	M	MP:0010025	decreased total body fat amount	Osbpl3<tm1a(EUCOMM)Wtsi>/Osbpl3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Osbpl3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700956	F	MP:0009709	hydrometra	Panx2<tm1b(KOMP)Wtsi>/Panx2<tm1b(KOMP)Wtsi>	C57BL/6N-Panx2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700956	F	MP:0001102	small superior vagus ganglion	Panx2<tm1b(KOMP)Wtsi>/Panx2<tm1b(KOMP)Wtsi>	C57BL/6N-Panx2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700956	F	MP:0004906	enlarged uterus	Panx2<tm1b(KOMP)Wtsi>/Panx2<tm1b(KOMP)Wtsi>	C57BL/6N-Panx2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700956	M	MP:0004952	increased spleen weight	Panx2<tm1b(KOMP)Wtsi>/Panx2<tm1b(KOMP)Wtsi>	C57BL/6N-Panx2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5700964	M	MP:0008806	increased circulating amylase level	Prrt2<tm1a(KOMP)Wtsi>/Prrt2<tm1a(KOMP)Wtsi>	C57BL/6N-Prrt2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700981	M	MP:0002135	abnormal kidney morphology	Rspo1<tm1.1(KOMP)Vlcg>/Rspo1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rspo1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700981	F	MP:0002098	abnormal vibrissa morphology	Rspo1<tm1.1(KOMP)Vlcg>/Rspo1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rspo1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700981	M	MP:0002175	decreased brain weight	Rspo1<tm1.1(KOMP)Vlcg>/Rspo1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rspo1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700981	M	MP:0010025	decreased total body fat amount	Rspo1<tm1.1(KOMP)Vlcg>/Rspo1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rspo1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700981	M	MP:0003960	increased lean body mass	Rspo1<tm1.1(KOMP)Vlcg>/Rspo1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rspo1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700981	M	MP:0001147	small testis	Rspo1<tm1.1(KOMP)Vlcg>/Rspo1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rspo1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700981	M	MP:0010123	increased bone mineral content	Rspo1<tm1.1(KOMP)Vlcg>/Rspo1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rspo1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700981	M	MP:0001146	abnormal testis morphology	Rspo1<tm1.1(KOMP)Vlcg>/Rspo1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rspo1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700981	M	MP:0010052	increased grip strength	Rspo1<tm1.1(KOMP)Vlcg>/Rspo1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rspo1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700981	F	MP:0001926	female infertility	Rspo1<tm1.1(KOMP)Vlcg>/Rspo1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rspo1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700987	M	MP:0001925	male infertility	Septin10<tm1a(KOMP)Wtsi>/Septin10<tm1a(KOMP)Wtsi>	C57BL/6N-Septin10<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5700996	M	MP:0004931	enlarged epididymis	Slitrk1<tm1.1(KOMP)Vlcg>/Slitrk1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slitrk1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700996	F	MP:0005343	increased circulating aspartate transaminase level	Slitrk1<tm1.1(KOMP)Vlcg>/Slitrk1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slitrk1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700996	M	MP:0002631	abnormal epididymis morphology	Slitrk1<tm1.1(KOMP)Vlcg>/Slitrk1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slitrk1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700996	F	MP:0001513	limb grasping	Slitrk1<tm1.1(KOMP)Vlcg>/Slitrk1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slitrk1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700996	F	MP:0002941	increased circulating alanine transaminase level	Slitrk1<tm1.1(KOMP)Vlcg>/Slitrk1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slitrk1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700996	M	MP:0001146	abnormal testis morphology	Slitrk1<tm1.1(KOMP)Vlcg>/Slitrk1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slitrk1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5700996	M	MP:0001147	small testis	Slitrk1<tm1.1(KOMP)Vlcg>/Slitrk1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slitrk1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701001	M	MP:0002764	short tibia	Spata6<tm1b(KOMP)Wtsi>/Spata6<tm1b(KOMP)Wtsi>	C57BL/6N-Spata6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5701001	M	MP:0001925	male infertility	Spata6<tm1b(KOMP)Wtsi>/Spata6<tm1b(KOMP)Wtsi>	C57BL/6N-Spata6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5701003	M	MP:0005650	abnormal limb bud morphology	Sufu<tm1b(KOMP)Wtsi>/Sufu<tm1b(KOMP)Wtsi>	C57BL/6N-Sufu<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5701003	M	MP:0002092	abnormal eye morphology	Sufu<tm1b(KOMP)Wtsi>/Sufu<tm1b(KOMP)Wtsi>	C57BL/6N-Sufu<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5701003	M	MP:0001722	pale yolk sac	Sufu<tm1b(KOMP)Wtsi>/Sufu<tm1b(KOMP)Wtsi>	C57BL/6N-Sufu<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5701003	M	MP:0003717	pallor	Sufu<tm1b(KOMP)Wtsi>/Sufu<tm1b(KOMP)Wtsi>	C57BL/6N-Sufu<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5701003	M	MP:0000603	pale liver	Sufu<tm1b(KOMP)Wtsi>/Sufu<tm1b(KOMP)Wtsi>	C57BL/6N-Sufu<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5701003	M	MP:0004258	abnormal placenta size	Sufu<tm1b(KOMP)Wtsi>/Sufu<tm1b(KOMP)Wtsi>	C57BL/6N-Sufu<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5701003	M	MP:0004848	abnormal liver size	Sufu<tm1b(KOMP)Wtsi>/Sufu<tm1b(KOMP)Wtsi>	C57BL/6N-Sufu<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5701010	F	MP:0005566	decreased blood urea nitrogen level	Tatdn3<tm1a(EUCOMM)Wtsi>/Tatdn3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tatdn3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701013	F	MP:0005358	abnormal incisor morphology	Tchp<tm1a(EUCOMM)Wtsi>/Tchp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tchp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701013	M	MP:0000182	increased circulating LDL cholesterol level	Tchp<tm1a(EUCOMM)Wtsi>/Tchp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tchp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701013	M	MP:0005178	increased circulating cholesterol level	Tchp<tm1a(EUCOMM)Wtsi>/Tchp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tchp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701013	M	MP:0001556	increased circulating HDL cholesterol level	Tchp<tm1a(EUCOMM)Wtsi>/Tchp<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tchp<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701015	M	MP:0011940	decreased food intake	Dynlt2b<tm1e(EUCOMM)Wtsi>/Dynlt2b<tm1e(EUCOMM)Wtsi>	C57BL/6N-Dynlt2b<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701015	M	MP:0001925	male infertility	Dynlt2b<tm1e(EUCOMM)Wtsi>/Dynlt2b<tm1e(EUCOMM)Wtsi>	C57BL/6N-Dynlt2b<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701016	F	MP:0005343	increased circulating aspartate transaminase level	Spmip9<tm1.1(KOMP)Vlcg>/Spmip9<tm1.1(KOMP)Vlcg>	C57BL/6N-Spmip9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701017	M	MP:0003960	increased lean body mass	Tgm6<tm1a(KOMP)Wtsi>/Tgm6<tm1a(KOMP)Wtsi>	C57BL/6N-Tgm6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701017	M	MP:0005419	decreased circulating serum albumin level	Tgm6<tm1a(KOMP)Wtsi>/Tgm6<tm1a(KOMP)Wtsi>	C57BL/6N-Tgm6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701017	M	MP:0005292	improved glucose tolerance	Tgm6<tm1a(KOMP)Wtsi>/Tgm6<tm1a(KOMP)Wtsi>	C57BL/6N-Tgm6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701018	M	MP:0001147	small testis	Tmem119<tm1.1(KOMP)Vlcg>/Tmem119<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem119<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701018	M	MP:0001146	abnormal testis morphology	Tmem119<tm1.1(KOMP)Vlcg>/Tmem119<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem119<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701019	M	MP:0000745	tremors	Tmem127<tm1(KOMP)Wtsi>/Tmem127<tm1(KOMP)Wtsi>	C57BL/6N-Tmem127<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701019	F	MP:0010123	increased bone mineral content	Tmem127<tm1(KOMP)Wtsi>/Tmem127<tm1(KOMP)Wtsi>	C57BL/6N-Tmem127<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701019	F	MP:0005344	increased circulating bilirubin level	Tmem127<tm1(KOMP)Wtsi>/Tmem127<tm1(KOMP)Wtsi>	C57BL/6N-Tmem127<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701019	M	MP:0012767	increased KLRG1-positive NK cell number	Tmem127<tm1(KOMP)Wtsi>/Tmem127<tm1(KOMP)Wtsi>	C57BL/6N-Tmem127<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701019	F	MP:0005553	increased circulating creatinine level	Tmem127<tm1(KOMP)Wtsi>/Tmem127<tm1(KOMP)Wtsi>	C57BL/6N-Tmem127<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701019	F	MP:0002968	increased circulating alkaline phosphatase level	Tmem127<tm1(KOMP)Wtsi>/Tmem127<tm1(KOMP)Wtsi>	C57BL/6N-Tmem127<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701019	M	MP:0008074	increased CD4-positive, alpha-beta T cell number	Tmem127<tm1(KOMP)Wtsi>/Tmem127<tm1(KOMP)Wtsi>	C57BL/6N-Tmem127<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701019	F	MP:0000579	abnormal nail morphology	Tmem127<tm1(KOMP)Wtsi>/Tmem127<tm1(KOMP)Wtsi>	C57BL/6N-Tmem127<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701020	F	MP:0001325	abnormal retina morphology	Peds1<tm1a(KOMP)Wtsi>/Peds1<tm1a(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Peds1<tm1a(KOMP)Wtsi> Tyr<c-Brd>/Wtsi	N	MGI:5576271
MGI:5701020	F	MP:0003961	decreased lean body mass	Peds1<tm1a(KOMP)Wtsi>/Peds1<tm1a(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Peds1<tm1a(KOMP)Wtsi> Tyr<c-Brd>/Wtsi	N	MGI:5576271
MGI:5701020	F	MP:0000063	decreased bone mineral density	Peds1<tm1a(KOMP)Wtsi>/Peds1<tm1a(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Peds1<tm1a(KOMP)Wtsi> Tyr<c-Brd>/Wtsi	N	MGI:5576271
MGI:5701020	F	MP:0002590	increased mean corpuscular volume	Peds1<tm1a(KOMP)Wtsi>/Peds1<tm1a(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Peds1<tm1a(KOMP)Wtsi> Tyr<c-Brd>/Wtsi	N	MGI:5576271
MGI:5701020	F	MP:0010096	abnormal incisor color	Peds1<tm1a(KOMP)Wtsi>/Peds1<tm1a(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Peds1<tm1a(KOMP)Wtsi> Tyr<c-Brd>/Wtsi	N	MGI:5576271
MGI:5701020	F	MP:0010088	decreased circulating fructosamine level	Peds1<tm1a(KOMP)Wtsi>/Peds1<tm1a(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Peds1<tm1a(KOMP)Wtsi> Tyr<c-Brd>/Wtsi	N	MGI:5576271
MGI:5701021	F	MP:0001529	abnormal vocalization	Tmem256<tm1.1(KOMP)Vlcg>/Tmem256<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem256<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701021	F	MP:0000208	decreased hematocrit	Tmem256<tm1.1(KOMP)Vlcg>/Tmem256<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem256<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701021	F	MP:0003795	abnormal bone structure	Tmem256<tm1.1(KOMP)Vlcg>/Tmem256<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem256<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701021	F	MP:0005562	decreased mean corpuscular hemoglobin	Tmem256<tm1.1(KOMP)Vlcg>/Tmem256<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem256<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701021	M	MP:0001513	limb grasping	Tmem256<tm1.1(KOMP)Vlcg>/Tmem256<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem256<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701021	M	MP:0000220	increased monocyte cell number	Tmem256<tm1.1(KOMP)Vlcg>/Tmem256<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem256<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701021	F	MP:0002874	decreased hemoglobin content	Tmem256<tm1.1(KOMP)Vlcg>/Tmem256<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem256<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701021	F	MP:0010511	shortened PR interval	Tmem256<tm1.1(KOMP)Vlcg>/Tmem256<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem256<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701030	M	MP:0001340	abnormal eyelid morphology	Tuft1<tm1a(KOMP)Wtsi>/Tuft1<tm1a(KOMP)Wtsi>	C57BL/6N-Tuft1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701030	F	MP:0002098	abnormal vibrissa morphology	Tuft1<tm1a(KOMP)Wtsi>/Tuft1<tm1a(KOMP)Wtsi>	C57BL/6N-Tuft1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701030	M	MP:0000186	decreased circulating HDL cholesterol level	Tuft1<tm1a(KOMP)Wtsi>/Tuft1<tm1a(KOMP)Wtsi>	C57BL/6N-Tuft1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701032	M	MP:0000598	abnormal liver morphology	Unc119<tm1.1(KOMP)Vlcg>/Unc119<tm1.1(KOMP)Vlcg>	C57BL/6N-Unc119<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701043	F	MP:0001314	cornea opacity	Zdhhc23<tm1.1(KOMP)Vlcg>/Zdhhc23<tm1.1(KOMP)Vlcg>	C57BL/6N-Zdhhc23<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701043	M	MP:0005505	thrombocytosis	Zdhhc23<tm1.1(KOMP)Vlcg>/Zdhhc23<tm1.1(KOMP)Vlcg>	C57BL/6N-Zdhhc23<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701043	F	MP:0001399	hyperactivity	Zdhhc23<tm1.1(KOMP)Vlcg>/Zdhhc23<tm1.1(KOMP)Vlcg>	C57BL/6N-Zdhhc23<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5701047	F	MP:0002075	abnormal coat/hair pigmentation	Zswim5<tm1.1(KOMP)Wtsi>/Zswim5<tm1.1(KOMP)Wtsi>	C57BL/6N-Zswim5<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5701687	M	MP:0005459	decreased percent body fat/body weight	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0003949	abnormal circulating lipid level	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0001552	increased circulating triglyceride level	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0001554	increased circulating free fatty acids level	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0004889	increased energy expenditure	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0002079	increased circulating insulin level	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0002628	hepatic steatosis	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0003960	increased lean body mass	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0030016	increased adipocyte glucose uptake	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0001399	hyperactivity	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0009117	abnormal white fat cell morphology	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0000005	increased brown adipose tissue amount	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0001783	decreased white adipose tissue amount	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0009133	decreased white fat cell size	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0005670	abnormal white adipose tissue physiology	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0002970	abnormal white adipose tissue morphology	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0005289	increased oxygen consumption	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0002941	increased circulating alanine transaminase level	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0011019	abnormal adaptive thermogenesis	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701687	M	MP:0010379	decreased respiratory quotient	Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz>,Tg(Fabp4-cre)#Abel/?	B6N.Cg-Cidec<tm1.1Gonz>/Cidec<tm1.2Gonz> Tg(Fabp4-cre)#Abel	N	25477509
MGI:5701798	M	MP:0005562	decreased mean corpuscular hemoglobin	Pld3<tm1e(EUCOMM)Wtsi>/Pld3<tm1e(EUCOMM)Wtsi>	C57BL/6N-Pld3<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5701798	F	MP:0003179	thrombocytopenia	Pld3<tm1e(EUCOMM)Wtsi>/Pld3<tm1e(EUCOMM)Wtsi>	C57BL/6N-Pld3<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5702409	F	MP:0010053	decreased grip strength	Sacs<tm2Bebr>/Sacs<tm2Bebr>	involves: C57BL/6	N	25260547
MGI:5702448	M	MP:0001925	male infertility	Gt(ROSA)26Sor<tm2.1(CAG-EGFP,-DTA*G128D)Pjen>/Gt(ROSA)26Sor<tm2.1(CAG-EGFP,-DTA*G128D)Pjen>	B6.Cg-Gt(ROSA)26Sor<tm2.1(CAG-EGFP,-DTA*G128D)Pjen>/J	N	MGI:3606206
MGI:5702941	M	MP:0002066	abnormal motor capabilities/coordination/movement	Mecp2<tm4.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702941	M	MP:0001262	decreased body weight	Mecp2<tm4.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702941	M	MP:0002804	abnormal motor learning	Mecp2<tm4.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702941	M	MP:0001364	decreased anxiety-related response	Mecp2<tm4.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702941	M	MP:0004924	abnormal behavior	Mecp2<tm4.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702941	M	MP:0002083	premature death	Mecp2<tm4.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702951	M	MP:0002066	abnormal motor capabilities/coordination/movement	Mecp2<tm5.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702951	M	MP:0001364	decreased anxiety-related response	Mecp2<tm5.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702951	M	MP:0002083	premature death	Mecp2<tm5.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702951	M	MP:0001262	decreased body weight	Mecp2<tm5.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702951	M	MP:0004924	abnormal behavior	Mecp2<tm5.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702952	M	MP:0001364	decreased anxiety-related response	Mecp2<tm6.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702952	M	MP:0004924	abnormal behavior	Mecp2<tm6.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702952	M	MP:0002804	abnormal motor learning	Mecp2<tm6.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702952	M	MP:0002066	abnormal motor capabilities/coordination/movement	Mecp2<tm6.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702952	M	MP:0001262	decreased body weight	Mecp2<tm6.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702952	M	MP:0002083	premature death	Mecp2<tm6.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702957	F	MP:0004924	abnormal behavior	Mecp2<tm6.1Bird>/Mecp2<+>	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702967	M	MP:0002066	abnormal motor capabilities/coordination/movement	Mecp2<tm3.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702967	M	MP:0001262	decreased body weight	Mecp2<tm3.1Bird>/Y	involves: 129P2/OlaHsd * C57BL/6	N	26647311
MGI:5702974	M	MP:0005389	reproductive system phenotype	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6J * FVB/N	Y	25474150
MGI:5702983	M	MP:0004930	small epididymis	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5702983	M	MP:0002675	asthenozoospermia	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5702983	M	MP:0014052	increased male germ cell apoptosis	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5702983	M	MP:0008892	abnormal sperm flagellum morphology	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5702983	M	MP:0001922	reduced male fertility	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5702983	M	MP:0020451	decreased sperm progressive motility	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5702983	M	MP:0004901	decreased male germ cell number	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5702983	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5702983	M	MP:0009230	abnormal sperm head morphology	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5702983	M	MP:0004852	decreased testis weight	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5702983	M	MP:0009238	coiled sperm flagellum	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5702983	M	MP:0002687	oligozoospermia	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5702983	M	MP:0001147	small testis	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5702983	M	MP:0009248	small caput epididymis	Ranbp9<tm1Wyan>/Ranbp9<tm1Wyan>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	25474150
MGI:5703004	M	MP:0005159	azoospermia	Ranbp9<tm1.1Wyan>/Ranbp9<tm1.1Wyan>	Not Specified	N	25474150
MGI:5703004	M	MP:0014052	increased male germ cell apoptosis	Ranbp9<tm1.1Wyan>/Ranbp9<tm1.1Wyan>	Not Specified	N	25474150
MGI:5703004	M	MP:0004901	decreased male germ cell number	Ranbp9<tm1.1Wyan>/Ranbp9<tm1.1Wyan>	Not Specified	N	25474150
MGI:5703004	M	MP:0001925	male infertility	Ranbp9<tm1.1Wyan>/Ranbp9<tm1.1Wyan>	Not Specified	N	25474150
MGI:5703659	M	MP:0003461	abnormal response to novel object	Fmr1<tm1Cgr>/Y,Tg(ACTB-Eif4e)#Ppp/0	involves: 129P2/OlaHsd * C57BL/6	N	26306459
MGI:5703659	M	MP:0001399	hyperactivity	Fmr1<tm1Cgr>/Y,Tg(ACTB-Eif4e)#Ppp/0	involves: 129P2/OlaHsd * C57BL/6	N	26306459
MGI:5703659	M	MP:0001360	abnormal social investigation	Fmr1<tm1Cgr>/Y,Tg(ACTB-Eif4e)#Ppp/0	involves: 129P2/OlaHsd * C57BL/6	N	26306459
MGI:5703659	M	MP:0001363	increased anxiety-related response	Fmr1<tm1Cgr>/Y,Tg(ACTB-Eif4e)#Ppp/0	involves: 129P2/OlaHsd * C57BL/6	N	26306459
MGI:5703659	M	MP:0002152	abnormal brain morphology	Fmr1<tm1Cgr>/Y,Tg(ACTB-Eif4e)#Ppp/0	involves: 129P2/OlaHsd * C57BL/6	N	26306459
MGI:5703659	M	MP:0001469	abnormal contextual conditioning behavior	Fmr1<tm1Cgr>/Y,Tg(ACTB-Eif4e)#Ppp/0	involves: 129P2/OlaHsd * C57BL/6	N	26306459
MGI:5703659	M	MP:0001409	increased stereotypic behavior	Fmr1<tm1Cgr>/Y,Tg(ACTB-Eif4e)#Ppp/0	involves: 129P2/OlaHsd * C57BL/6	N	26306459
MGI:5703659	M	MP:0001463	abnormal spatial learning	Fmr1<tm1Cgr>/Y,Tg(ACTB-Eif4e)#Ppp/0	involves: 129P2/OlaHsd * C57BL/6	N	26306459
MGI:5703660	M	MP:0002152	abnormal brain morphology	Tg(ACTB-Eif4e)#Ppp/0	involves: C57BL/6	N	26306459
MGI:5703660	M	MP:0001360	abnormal social investigation	Tg(ACTB-Eif4e)#Ppp/0	involves: C57BL/6	N	26306459
MGI:5703660	M	MP:0031391	increased locomotor activity	Tg(ACTB-Eif4e)#Ppp/0	involves: C57BL/6	N	26306459
MGI:5703660	M	MP:0001409	increased stereotypic behavior	Tg(ACTB-Eif4e)#Ppp/0	involves: C57BL/6	N	26306459
MGI:5703970	F	MP:0002871	albuminuria	Asb4<tm1.2Cpat>/Asb4<tm1.2Cpat>	involves: 129/SvEv	N	27821757
MGI:5703970	F	MP:0001935	decreased litter size	Asb4<tm1.2Cpat>/Asb4<tm1.2Cpat>	involves: 129/SvEv	N	27821757
MGI:5703970	F	MP:0011320	abnormal glomerular capillary morphology	Asb4<tm1.2Cpat>/Asb4<tm1.2Cpat>	involves: 129/SvEv	N	27821757
MGI:5703970	F	MP:0009661	abnormal pregnancy	Asb4<tm1.2Cpat>/Asb4<tm1.2Cpat>	involves: 129/SvEv	N	27821757
MGI:5703970	F	MP:0010695	abnormal blood pressure regulation	Asb4<tm1.2Cpat>/Asb4<tm1.2Cpat>	involves: 129/SvEv	N	24586788
MGI:5703970	F	MP:0011339	abnormal glomerular mesangium morphology	Asb4<tm1.2Cpat>/Asb4<tm1.2Cpat>	involves: 129/SvEv	N	27821757
MGI:5703970	F	MP:0000231	hypertension	Asb4<tm1.2Cpat>/Asb4<tm1.2Cpat>	involves: 129/SvEv	N	27821757
MGI:5703970	F	MP:0020153	abnormal urine albumin level	Asb4<tm1.2Cpat>/Asb4<tm1.2Cpat>	involves: 129/SvEv	N	24586788
MGI:5704096	M	MP:0013894	abnormal behavioral response to amphetamine	Tg(Npy-EGFP/RNAi:Gad1)1Mirn/?	C57BL/6NHsd-Tg(Npy-EGFP/RNAi:Gad1)1Mirn	N	24322205
MGI:5704096	M	MP:0001364	decreased anxiety-related response	Tg(Npy-EGFP/RNAi:Gad1)1Mirn/?	C57BL/6NHsd-Tg(Npy-EGFP/RNAi:Gad1)1Mirn	N	24322205
MGI:5704096	M	MP:0001360	abnormal social investigation	Tg(Npy-EGFP/RNAi:Gad1)1Mirn/?	C57BL/6NHsd-Tg(Npy-EGFP/RNAi:Gad1)1Mirn	N	24322205
MGI:5704119	M	MP:0003462	abnormal response to novel odor	Tg(Cck-EGFP/RNAi:Gad1)2Mirn/?	C57BL/6NHsd-Tg(Cck-EGFP/RNAi:Gad1)2Mirn	N	24322205
MGI:5704119	M	MP:0013894	abnormal behavioral response to amphetamine	Tg(Cck-EGFP/RNAi:Gad1)2Mirn/?	C57BL/6NHsd-Tg(Cck-EGFP/RNAi:Gad1)2Mirn	N	24322205
MGI:5704119	M	MP:0001402	decreased locomotor activity	Tg(Cck-EGFP/RNAi:Gad1)2Mirn/?	C57BL/6NHsd-Tg(Cck-EGFP/RNAi:Gad1)2Mirn	N	24322205
MGI:5704169	M	MP:0012318	slow extinction of fear memory	Tg(Cnr1-EGFP/RNAi:Gad1)1Mirn/?	C57BL/6-Tg(Cnr1-EGFP/RNAi:Gad1)1Mirn	N	24239560
MGI:5704169	M	MP:0013894	abnormal behavioral response to amphetamine	Tg(Cnr1-EGFP/RNAi:Gad1)1Mirn/?	C57BL/6-Tg(Cnr1-EGFP/RNAi:Gad1)1Mirn	N	24239560
MGI:5704169	M	MP:0010069	increased serotonin level	Tg(Cnr1-EGFP/RNAi:Gad1)1Mirn/?	C57BL/6-Tg(Cnr1-EGFP/RNAi:Gad1)1Mirn	N	24239560
MGI:5704169	M	MP:0001360	abnormal social investigation	Tg(Cnr1-EGFP/RNAi:Gad1)1Mirn/?	C57BL/6-Tg(Cnr1-EGFP/RNAi:Gad1)1Mirn	N	24239560
MGI:5704169	M	MP:0009455	enhanced cued conditioning behavior	Tg(Cnr1-EGFP/RNAi:Gad1)1Mirn/?	C57BL/6-Tg(Cnr1-EGFP/RNAi:Gad1)1Mirn	N	24239560
MGI:5704169	M	MP:0001488	increased startle reflex	Tg(Cnr1-EGFP/RNAi:Gad1)1Mirn/?	C57BL/6-Tg(Cnr1-EGFP/RNAi:Gad1)1Mirn	N	24239560
MGI:5704175	M	MP:0003461	abnormal response to novel object	Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn/?	C57BL/6-Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn	N	25623945
MGI:5704175	M	MP:0002757	decreased vertical activity	Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn/?	C57BL/6-Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn	N	25623945
MGI:5704175	M	MP:0001360	abnormal social investigation	Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn/?	C57BL/6-Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn	N	25623945
MGI:5704175	M	MP:0012318	slow extinction of fear memory	Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn/?	C57BL/6-Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn	N	25623945
MGI:5704175	M	MP:0004008	abnormal GABA-mediated receptor currents	Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn/?	C57BL/6-Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn	N	25623945
MGI:5704175	M	MP:0002574	increased vertical activity	Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn/?	C57BL/6-Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn	N	25623945
MGI:5704175	M	MP:0009142	decreased prepulse inhibition	Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn/?	C57BL/6-Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn	N	25623945
MGI:5704175	M	MP:0001488	increased startle reflex	Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn/?	C57BL/6-Tg(Pvalb-tdTomato/RNAi:Gad1)3Mirn	N	25623945
MGI:5704295	M	MP:0005179	decreased circulating cholesterol level	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0031414	decreased skeletal muscle triglyceride level	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0031417	decreased cardiac muscle triglyceride level	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0009289	decreased epididymal fat pad weight	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0009122	decreased white fat cell lipid droplet size	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0005318	decreased triglyceride level	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0005560	decreased circulating glucose level	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0003884	decreased macrophage cell number	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0005425	increased macrophage cell number	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0003982	increased cholesterol level	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0009133	decreased white fat cell size	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0003983	decreased cholesterol level	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0002727	decreased circulating insulin level	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0005292	improved glucose tolerance	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0010026	decreased liver cholesterol level	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0009356	decreased liver triglyceride level	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0002644	decreased circulating triglyceride level	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704295	M	MP:0002891	increased insulin sensitivity	Apoe<tm1.1Mae>/Apoe<tm1.1Mae>,Tg(Fabp4-cre)1Rev/0	B6.Cg-Apoe<tm1.1Mae> Tg(Fabp4-cre)1Rev	N	25421060
MGI:5704316	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Fgf13<tm1Jom>/Y	C57BL/6-Fgf13<tm1Jom>	N	26063919
MGI:5704317	F	MP:0001499	abnormal kindling response	Fgf13<tm1Jom>/Fgf13<+>	C57BL/6-Fgf13<tm1Jom>	N	26063919
MGI:5704317	F	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude	Fgf13<tm1Jom>/Fgf13<+>	C57BL/6-Fgf13<tm1Jom>	N	26063919
MGI:5704317	F	MP:0014378	increased excitatory postsynaptic current frequency	Fgf13<tm1Jom>/Fgf13<+>	C57BL/6-Fgf13<tm1Jom>	N	26063919
MGI:5704317	F	MP:0002945	abnormal inhibitory postsynaptic currents	Fgf13<tm1Jom>/Fgf13<+>	C57BL/6-Fgf13<tm1Jom>	N	26063919
MGI:5704317	F	MP:0009358	environmentally induced seizures	Fgf13<tm1Jom>/Fgf13<+>	C57BL/6-Fgf13<tm1Jom>	N	26063919
MGI:5704317	F	MP:0002064	seizures	Fgf13<tm1Jom>/Fgf13<+>	C57BL/6-Fgf13<tm1Jom>	N	26063919
MGI:5704317	F	MP:0002206	abnormal CNS synaptic transmission	Fgf13<tm1Jom>/Fgf13<+>	C57BL/6-Fgf13<tm1Jom>	N	26063919
MGI:5704363	F	MP:0002083	premature death	Dicer1<tm1Tara>/Dicer1<tm1Tara>,Pten<tm1Hwu>/Pten<tm1Hwu>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	22331912
MGI:5704363	F	MP:0002038	increased carcinoma incidence	Dicer1<tm1Tara>/Dicer1<tm1Tara>,Pten<tm1Hwu>/Pten<tm1Hwu>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	22331912
MGI:5704363	F	MP:0003574	abnormal oviduct morphology	Dicer1<tm1Tara>/Dicer1<tm1Tara>,Pten<tm1Hwu>/Pten<tm1Hwu>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	22331912
MGI:5704363	F	MP:0005324	ascites	Dicer1<tm1Tara>/Dicer1<tm1Tara>,Pten<tm1Hwu>/Pten<tm1Hwu>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	22331912
MGI:5704363	F	MP:0001272	increased metastatic potential	Dicer1<tm1Tara>/Dicer1<tm1Tara>,Pten<tm1Hwu>/Pten<tm1Hwu>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	22331912
MGI:5704363	F	MP:0003579	increased ovarian carcinoma incidence	Dicer1<tm1Tara>/Dicer1<tm1Tara>,Pten<tm1Hwu>/Pten<tm1Hwu>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	22331912
MGI:5704370	F	MP:0003579	increased ovarian carcinoma incidence	Dicer1<tm1Tara>/Dicer1<tm1Tara>,Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm2Tyj>/Trp53<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	25815421
MGI:5704370	F	MP:0002083	premature death	Dicer1<tm1Tara>/Dicer1<tm1Tara>,Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm2Tyj>/Trp53<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	25815421
MGI:5704370	F	MP:0002038	increased carcinoma incidence	Dicer1<tm1Tara>/Dicer1<tm1Tara>,Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm2Tyj>/Trp53<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	25815421
MGI:5704370	F	MP:0005324	ascites	Dicer1<tm1Tara>/Dicer1<tm1Tara>,Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm2Tyj>/Trp53<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	25815421
MGI:5704370	F	MP:0001272	increased metastatic potential	Dicer1<tm1Tara>/Dicer1<tm1Tara>,Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm2Tyj>/Trp53<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	25815421
MGI:5704372	F	MP:0003579	increased ovarian carcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm2Tyj>/Trp53<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	25815421
MGI:5704372	F	MP:0001272	increased metastatic potential	Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm2Tyj>/Trp53<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	25815421
MGI:5704372	F	MP:0012411	increased granulosa cell tumor incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm2Tyj>/Trp53<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	25815421
MGI:5704372	F	MP:0005324	ascites	Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm2Tyj>/Trp53<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	25815421
MGI:5704372	F	MP:0002083	premature death	Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm2Tyj>/Trp53<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	N	25815421
MGI:5704374	F	MP:0002006	neoplasm	Dicer1<tm1Tara>/Dicer1<tm1Tara>,Trp53<tm2Tyj>/Trp53<+>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	Y	25815421
MGI:5704375	F	MP:0002006	neoplasm	Dicer1<tm1Tara>/Dicer1<tm1Tara>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129P2/OlaHsd * 129S7/SvEvBrd	Y	25815421
MGI:5704376	F	MP:0002006	neoplasm	Amhr2<tm3(cre)Bhr>/Amhr2<+>,Trp53<tm2Tyj>/Trp53<+>	involves: 129S4/SvJae * 129S7/SvEvBrd	Y	25815421
MGI:5704407	M	MP:0005202	lethargy	Tg(Prnp-ATXN7*92Q)6529Als/Y	involves: C3H/HeJ * C57BL/6J	N	18054568
MGI:5704407	M	MP:0002816	colitis	Tg(Prnp-ATXN7*92Q)6529Als/Y	involves: C3H/HeJ * C57BL/6J	N	18054568
MGI:5704407	M	MP:0002083	premature death	Tg(Prnp-ATXN7*92Q)6529Als/Y	involves: C3H/HeJ * C57BL/6J	N	18054568
MGI:5704407	M	MP:0001046	abnormal enteric neuron morphology	Tg(Prnp-ATXN7*92Q)6529Als/Y	involves: C3H/HeJ * C57BL/6J	N	18054568
MGI:5704407	M	MP:0005404	abnormal axon morphology	Tg(Prnp-ATXN7*92Q)6529Als/Y	involves: C3H/HeJ * C57BL/6J	N	18054568
MGI:5704407	M	MP:0003270	intestinal obstruction	Tg(Prnp-ATXN7*92Q)6529Als/Y	involves: C3H/HeJ * C57BL/6J	N	18054568
MGI:5704407	M	MP:0011082	abnormal gastrointestinal motility	Tg(Prnp-ATXN7*92Q)6529Als/Y	involves: C3H/HeJ * C57BL/6J	N	18054568
MGI:5704407	M	MP:0001270	distended abdomen	Tg(Prnp-ATXN7*92Q)6529Als/Y	involves: C3H/HeJ * C57BL/6J	N	18054568
MGI:5704407	M	MP:0004191	neuronal intranuclear inclusions	Tg(Prnp-ATXN7*92Q)6529Als/Y	involves: C3H/HeJ * C57BL/6J	N	18054568
MGI:5704446	F	MP:0005386	behavior/neurological phenotype	Tg(Prnp-ATXN7*92Q)6529Als/0	involves: C3H/HeJ * C57BL/6J	Y	12077187
MGI:5704446	F	MP:0002090	abnormal vision	Tg(Prnp-ATXN7*92Q)6529Als/0	involves: C3H/HeJ * C57BL/6J	N	11580893
MGI:5704446	F	MP:0010768	mortality/aging	Tg(Prnp-ATXN7*92Q)6529Als/0	involves: C3H/HeJ * C57BL/6J	Y	18054568
MGI:5705076	M	MP:0001156	abnormal spermatogenesis	Rfx2<Gt(IST10638H11)Tigm>/Rfx2<Gt(IST10638H11)Tigm>	either: C57BL/6N-Rfx2<Gt(IST10638H11)Tigm> or (involves: C57BL/6N * CD-1)	N	26248850
MGI:5705076	M	MP:0013598	Leydig cell hypertrophy	Rfx2<Gt(IST10638H11)Tigm>/Rfx2<Gt(IST10638H11)Tigm>	either: C57BL/6N-Rfx2<Gt(IST10638H11)Tigm> or (involves: C57BL/6N * CD-1)	N	26248850
MGI:5705076	M	MP:0001932	abnormal spermiogenesis	Rfx2<Gt(IST10638H11)Tigm>/Rfx2<Gt(IST10638H11)Tigm>	either: C57BL/6N-Rfx2<Gt(IST10638H11)Tigm> or (involves: C57BL/6N * CD-1)	N	26248850
MGI:5705076	M	MP:0006380	abnormal spermatid morphology	Rfx2<Gt(IST10638H11)Tigm>/Rfx2<Gt(IST10638H11)Tigm>	either: C57BL/6N-Rfx2<Gt(IST10638H11)Tigm> or (involves: C57BL/6N * CD-1)	N	26248850
MGI:5705076	M	MP:0020550	multinucleated giant male germ cells	Rfx2<Gt(IST10638H11)Tigm>/Rfx2<Gt(IST10638H11)Tigm>	either: C57BL/6N-Rfx2<Gt(IST10638H11)Tigm> or (involves: C57BL/6N * CD-1)	N	26248850
MGI:5705076	M	MP:0001925	male infertility	Rfx2<Gt(IST10638H11)Tigm>/Rfx2<Gt(IST10638H11)Tigm>	either: C57BL/6N-Rfx2<Gt(IST10638H11)Tigm> or (involves: C57BL/6N * CD-1)	N	26248850
MGI:5705076	M	MP:0001152	increased Leydig cell number	Rfx2<Gt(IST10638H11)Tigm>/Rfx2<Gt(IST10638H11)Tigm>	either: C57BL/6N-Rfx2<Gt(IST10638H11)Tigm> or (involves: C57BL/6N * CD-1)	N	26248850
MGI:5705079	M	MP:0001922	reduced male fertility	Ddhd1<tm1Katn>/Ddhd1<tm1Katn>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24599962
MGI:5705080	M	MP:0009243	hairpin sperm flagellum	Ddhd1<tm1.1Katn>/Ddhd1<tm1.1Katn>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24599962
MGI:5705080	M	MP:0002675	asthenozoospermia	Ddhd1<tm1.1Katn>/Ddhd1<tm1.1Katn>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24599962
MGI:5705080	M	MP:0014464	decreased sperm mitochondrial sheath size	Ddhd1<tm1.1Katn>/Ddhd1<tm1.1Katn>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24599962
MGI:5705080	M	MP:0009237	kinked sperm flagellum	Ddhd1<tm1.1Katn>/Ddhd1<tm1.1Katn>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24599962
MGI:5705080	M	MP:0002687	oligozoospermia	Ddhd1<tm1.1Katn>/Ddhd1<tm1.1Katn>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24599962
MGI:5705080	M	MP:0005578	teratozoospermia	Ddhd1<tm1.1Katn>/Ddhd1<tm1.1Katn>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24599962
MGI:5705080	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Ddhd1<tm1.1Katn>/Ddhd1<tm1.1Katn>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24599962
MGI:5705080	M	MP:0009834	abnormal sperm annulus morphology	Ddhd1<tm1.1Katn>/Ddhd1<tm1.1Katn>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24599962
MGI:5705080	M	MP:0004852	decreased testis weight	Ddhd1<tm1.1Katn>/Ddhd1<tm1.1Katn>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24599962
MGI:5705080	M	MP:0001922	reduced male fertility	Ddhd1<tm1.1Katn>/Ddhd1<tm1.1Katn>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	24599962
MGI:5705236	M	MP:0005378	growth/size/body region phenotype	Irs4<tm1.1Mfw>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	24567904
MGI:5705236	M	MP:0005559	increased circulating glucose level	Irs4<tm1.1Mfw>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	24567904
MGI:5705236	M	MP:0005376	homeostasis/metabolism phenotype	Irs4<tm1.1Mfw>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	24567904
MGI:5705236	M	MP:0010768	mortality/aging	Irs4<tm1.1Mfw>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	24567904
MGI:5705238	M	MP:0001260	increased body weight	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705238	M	MP:0005290	decreased oxygen consumption	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705238	M	MP:0013279	increased fasting circulating glucose level	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705238	M	MP:0002628	hepatic steatosis	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705238	M	MP:0020234	decreased basal metabolism	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705238	M	MP:0005293	impaired glucose tolerance	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705238	M	MP:0005669	increased circulating leptin level	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705238	M	MP:0002078	abnormal glucose homeostasis	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705238	M	MP:0005331	insulin resistance	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705238	M	MP:0002079	increased circulating insulin level	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705238	M	MP:0009124	increased brown fat cell lipid droplet size	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705238	M	MP:0005452	abnormal adipose tissue amount	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705238	M	MP:0011939	increased food intake	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705238	M	MP:0005559	increased circulating glucose level	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705239	M	MP:0005378	growth/size/body region phenotype	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Lepr<tm3(cre)Mgmj>/Lepr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	24567904
MGI:5705239	M	MP:0005376	homeostasis/metabolism phenotype	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Irs4<tm1.1Mfw>/Y,Lepr<tm3(cre)Mgmj>/Lepr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	24567904
MGI:5705240	M	MP:0020234	decreased basal metabolism	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705240	M	MP:0005559	increased circulating glucose level	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705240	M	MP:0011939	increased food intake	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705240	M	MP:0005331	insulin resistance	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705240	M	MP:0005290	decreased oxygen consumption	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705240	M	MP:0002078	abnormal glucose homeostasis	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705240	M	MP:0005669	increased circulating leptin level	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705240	M	MP:0002079	increased circulating insulin level	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705240	M	MP:0013279	increased fasting circulating glucose level	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705240	M	MP:0005293	impaired glucose tolerance	Irs2<tm2Mfw>/Irs2<tm2Mfw>,Tg(Nes-cre)1Kln/?	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	24567904
MGI:5705314	F	MP:0009506	abnormal mammary gland alveolus morphology	Neat1<tm1.1Shna>/Neat1<tm1.1Shna>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	25316907
MGI:5705314	F	MP:0000627	abnormal mammary gland morphology	Neat1<tm1.1Shna>/Neat1<tm1.1Shna>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	25316907
MGI:5705314	F	MP:0009504	abnormal mammary gland epithelium morphology	Neat1<tm1.1Shna>/Neat1<tm1.1Shna>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	25316907
MGI:5705314	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Neat1<tm1.1Shna>/Neat1<tm1.1Shna>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	25316907
MGI:5705314	F	MP:0000662	abnormal branching of the mammary ductal tree	Neat1<tm1.1Shna>/Neat1<tm1.1Shna>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	25316907
MGI:5705314	F	MP:0001882	abnormal lactation	Neat1<tm1.1Shna>/Neat1<tm1.1Shna>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	25316907
MGI:5705314	F	MP:0000628	abnormal mammary gland development	Neat1<tm1.1Shna>/Neat1<tm1.1Shna>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	25316907
MGI:5705321	M	MP:0001158	abnormal prostate gland morphology	Kras<tm4Tyj>/Kras<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22350410
MGI:5705321	M	MP:0001272	increased metastatic potential	Kras<tm4Tyj>/Kras<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22350410
MGI:5705321	M	MP:0002083	premature death	Kras<tm4Tyj>/Kras<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22350410
MGI:5705321	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Kras<tm4Tyj>/Kras<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22350410
MGI:5705328	M	MP:0002083	premature death	Kras<tm4Tyj>/Kras<+>,Pten<tm1Hwu>/Pten<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22350410
MGI:5705328	M	MP:0001272	increased metastatic potential	Kras<tm4Tyj>/Kras<+>,Pten<tm1Hwu>/Pten<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22350410
MGI:5705328	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Kras<tm4Tyj>/Kras<+>,Pten<tm1Hwu>/Pten<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22350410
MGI:5705386	M	MP:0009838	abnormal sperm axoneme morphology	Bbs7<tm1Vcs>/Bbs7<tm1Vcs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23572516
MGI:5705386	M	MP:0001925	male infertility	Bbs7<tm1Vcs>/Bbs7<tm1Vcs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23572516
MGI:5705386	M	MP:0008545	absent sperm flagellum	Bbs7<tm1Vcs>/Bbs7<tm1Vcs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23572516
MGI:5705386	M	MP:0031356	abnormal outer dense fiber morphology	Bbs7<tm1Vcs>/Bbs7<tm1Vcs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23572516
MGI:5705386	M	MP:0008892	abnormal sperm flagellum morphology	Bbs7<tm1Vcs>/Bbs7<tm1Vcs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23572516
MGI:5705386	M	MP:0009836	abnormal sperm principal piece morphology	Bbs7<tm1Vcs>/Bbs7<tm1Vcs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	23572516
MGI:5705580	M	MP:0001147	small testis	Aey30/?	C3HeB/FeJ-Aey30	N	MGI:2655403
MGI:5705580	M	MP:0002687	oligozoospermia	Aey30/?	C3HeB/FeJ-Aey30	N	MGI:2655403
MGI:5705650	M	MP:0002083	premature death	Tg(Pbsn-ERG*)1Vv/0	involves: 129S1/SvImJ * C57BL/6J * CBA	N	26058078
MGI:5705650	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(Pbsn-ERG*)1Vv/0	involves: 129S1/SvImJ * C57BL/6J * CBA	N	26058078
MGI:5705650	M	MP:0010357	increased prostate gland tumor incidence	Tg(Pbsn-ERG*)1Vv/0	involves: 129S1/SvImJ * C57BL/6J * CBA	N	26058078
MGI:5705651	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Col1a1<tm1(tetO-YAP1*)Fcam>/Col1a1<+>,Gt(ROSA)26Sor<tm1(rtTA,EGFP)Nagy>/Gt(ROSA)26Sor<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * DBA/2	N	26058078
MGI:5705651	M	MP:0010357	increased prostate gland tumor incidence	Col1a1<tm1(tetO-YAP1*)Fcam>/Col1a1<+>,Gt(ROSA)26Sor<tm1(rtTA,EGFP)Nagy>/Gt(ROSA)26Sor<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * DBA/2	N	26058078
MGI:5705944	M	MP:0010052	increased grip strength	Armh3<tm1a(EUCOMM)Wtsi>/Armh3<+>	C57BL/6N-Armh3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705945	M	MP:0002833	increased heart weight	Actn4<tm1a(EUCOMM)Wtsi>/Actn4<+>	C57BL/6N-Actn4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705946	M	MP:0003443	increased circulating glycerol level	Actr6<tm1a(EUCOMM)Wtsi>/Actr6<+>	C57BL/6N-Actr6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705947	F	MP:0005568	increased circulating total protein level	Acvr1<tm1.1(KOMP)Vlcg>/Acvr1<+>	C57BL/6N-Acvr1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5705948	M	MP:0002135	abnormal kidney morphology	Acvr2b<tm1.1(KOMP)Vlcg>/Acvr2b<+>	C57BL/6N-Acvr2b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705948	M	MP:0003068	enlarged kidney	Acvr2b<tm1.1(KOMP)Vlcg>/Acvr2b<+>	C57BL/6N-Acvr2b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705948	M	MP:0008528	polycystic kidney	Acvr2b<tm1.1(KOMP)Vlcg>/Acvr2b<+>	C57BL/6N-Acvr2b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705949	M	MP:0000221	decreased leukocyte cell number	Adgrb1<tm2a(EUCOMM)Wtsi>/Adgrb1<+>	C57BL/6N-Adgrb1<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705950	M	MP:0001147	small testis	Adra2a<tm1.1(KOMP)Vlcg>/Adra2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Adra2a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705950	F	MP:0013278	decreased fasting circulating glucose level	Adra2a<tm1.1(KOMP)Vlcg>/Adra2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Adra2a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705950	M	MP:0001146	abnormal testis morphology	Adra2a<tm1.1(KOMP)Vlcg>/Adra2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Adra2a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705951	M	MP:0004599	abnormal vertebral arch morphology	Aff3<tm1a(EUCOMM)Wtsi>/Aff3<+>	C57BL/6N-Aff3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705954	M	MP:0004952	increased spleen weight	Arf4<tm1b(KOMP)Wtsi>/Arf4<+>	C57BL/6N-Arf4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5705954	M	MP:0000266	abnormal heart morphology	Arf4<tm1b(KOMP)Wtsi>/Arf4<+>	C57BL/6N-Arf4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5705954	M	MP:0000689	abnormal spleen morphology	Arf4<tm1b(KOMP)Wtsi>/Arf4<+>	C57BL/6N-Arf4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5705954	M	MP:0000691	enlarged spleen	Arf4<tm1b(KOMP)Wtsi>/Arf4<+>	C57BL/6N-Arf4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5705954	M	MP:0000274	enlarged heart	Arf4<tm1b(KOMP)Wtsi>/Arf4<+>	C57BL/6N-Arf4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5705956	F	MP:0002060	abnormal skin morphology	Atf6b<tm1.1(KOMP)Vlcg>/Atf6b<+>	C57BL/6N-Atf6b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705956	F	MP:0001192	scaly skin	Atf6b<tm1.1(KOMP)Vlcg>/Atf6b<+>	C57BL/6N-Atf6b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705960	F	MP:0004122	abnormal sinus arrhythmia	Casq2<tm1b(KOMP)Wtsi>/Casq2<+>	C57BL/6N-Casq2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5705960	F	MP:0003929	decreased heart rate variability	Casq2<tm1b(KOMP)Wtsi>/Casq2<+>	C57BL/6N-Casq2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5705960	F	MP:0005385	cardiovascular system phenotype	Casq2<tm1b(KOMP)Wtsi>/Casq2<+>	C57BL/6N-Casq2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5705961	M	MP:0010052	increased grip strength	Ccdc122<tm1a(KOMP)Wtsi>/Ccdc122<+>	C57BL/6N-Ccdc122<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705962	F	MP:0010052	increased grip strength	Ccdc134<tm1a(KOMP)Wtsi>/Ccdc134<+>	C57BL/6N-Ccdc134<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705963	F	MP:0001126	abnormal ovary morphology	Terb1<tm1b(KOMP)Mbp>/Terb1<+>	C57BL/6N-Terb1<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5705963	F	MP:0002941	increased circulating alanine transaminase level	Terb1<tm1b(KOMP)Mbp>/Terb1<+>	C57BL/6N-Terb1<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5705963	F	MP:0000703	abnormal thymus morphology	Terb1<tm1b(KOMP)Mbp>/Terb1<+>	C57BL/6N-Terb1<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5705963	F	MP:0000709	enlarged thymus	Terb1<tm1b(KOMP)Mbp>/Terb1<+>	C57BL/6N-Terb1<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5705964	F	MP:0010053	decreased grip strength	Ccdc92<tm1b(KOMP)Mbp>/Ccdc92<tm1b(KOMP)Mbp>	C57BL/6N-Ccdc92<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5705964	M	MP:0002175	decreased brain weight	Ccdc92<tm1b(KOMP)Mbp>/Ccdc92<tm1b(KOMP)Mbp>	C57BL/6N-Ccdc92<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5705973	F	MP:0005562	decreased mean corpuscular hemoglobin	Cert1<tm1a(KOMP)Wtsi>/Cert1<+>	C57BL/6N-Cert1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705975	F	MP:0002098	abnormal vibrissa morphology	Crb2<tm1a(KOMP)Wtsi>/Crb2<+>	C57BL/6N-Crb2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705976	F	MP:0002968	increased circulating alkaline phosphatase level	Creb3l1<tm1e(EUCOMM)Wtsi>/Creb3l1<+>	C57BL/6N-Creb3l1<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705977	M	MP:0000063	decreased bone mineral density	Crispld2<tm1.1(KOMP)Vlcg>/Crispld2<+>	C57BL/6N-Crispld2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705977	M	MP:0002644	decreased circulating triglyceride level	Crispld2<tm1.1(KOMP)Vlcg>/Crispld2<+>	C57BL/6N-Crispld2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705978	F	MP:0001258	decreased body length	Crtc3<tm1b(KOMP)Wtsi>/Crtc3<+>	C57BL/6N-Crtc3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5705979	F	MP:0009709	hydrometra	Csf3r<tm1.1(KOMP)Vlcg>/Csf3r<+>	C57BL/6N-Csf3r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705979	F	MP:0001102	small superior vagus ganglion	Csf3r<tm1.1(KOMP)Vlcg>/Csf3r<+>	C57BL/6N-Csf3r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705979	M	MP:0001146	abnormal testis morphology	Csf3r<tm1.1(KOMP)Vlcg>/Csf3r<+>	C57BL/6N-Csf3r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705979	M	MP:0000266	abnormal heart morphology	Csf3r<tm1.1(KOMP)Vlcg>/Csf3r<+>	C57BL/6N-Csf3r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705979	M	MP:0001147	small testis	Csf3r<tm1.1(KOMP)Vlcg>/Csf3r<+>	C57BL/6N-Csf3r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705979	M	MP:0000274	enlarged heart	Csf3r<tm1.1(KOMP)Vlcg>/Csf3r<+>	C57BL/6N-Csf3r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705980	F	MP:0005553	increased circulating creatinine level	Cxcr2<tm1a(EUCOMM)Wtsi>/Cxcr2<+>	C57BL/6N-Cxcr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705982	M	MP:0000218	increased leukocyte cell number	Dbn1<tm1a(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705983	F	MP:0010052	increased grip strength	Dclk1<tm1a(EUCOMM)Wtsi>/Dclk1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dclk1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705983	F	MP:0005343	increased circulating aspartate transaminase level	Dclk1<tm1a(EUCOMM)Wtsi>/Dclk1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dclk1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705983	F	MP:0010093	decreased circulating magnesium level	Dclk1<tm1a(EUCOMM)Wtsi>/Dclk1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dclk1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705983	F	MP:0001258	decreased body length	Dclk1<tm1a(EUCOMM)Wtsi>/Dclk1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dclk1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705984	F	MP:0005553	increased circulating creatinine level	Dctn1<tm1a(EUCOMM)Wtsi>/Dctn1<+>	C57BL/6N-Dctn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705985	M	MP:0000062	increased bone mineral density	Dlg3<tm1a(EUCOMM)Wtsi>/Y	C57BL/6N-Dlg3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705987	M	MP:0005179	decreased circulating cholesterol level	Dmxl2<tm1a(EUCOMM)Wtsi>/Dmxl2<+>	C57BL/6N-A<tm1Brd> Dmxl2<tm1a(EUCOMM)Wtsi>/WtsiH	N	MGI:5576271
MGI:5705987	F	MP:0010024	increased total body fat amount	Dmxl2<tm1a(EUCOMM)Wtsi>/Dmxl2<+>	C57BL/6N-A<tm1Brd> Dmxl2<tm1a(EUCOMM)Wtsi>/WtsiH	N	MGI:5576271
MGI:5705987	F	MP:0003961	decreased lean body mass	Dmxl2<tm1a(EUCOMM)Wtsi>/Dmxl2<+>	C57BL/6N-A<tm1Brd> Dmxl2<tm1a(EUCOMM)Wtsi>/WtsiH	N	MGI:5576271
MGI:5705987	F	MP:0010124	decreased bone mineral content	Dmxl2<tm1a(EUCOMM)Wtsi>/Dmxl2<+>	C57BL/6N-A<tm1Brd> Dmxl2<tm1a(EUCOMM)Wtsi>/WtsiH	N	MGI:5576271
MGI:5705990	F	MP:0005633	increased circulating sodium level	Dpy30<tm1a(KOMP)Wtsi>/Dpy30<+>	C57BL/6N-Dpy30<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705991	M	MP:0005292	improved glucose tolerance	Dspp<tm1.1(KOMP)Vlcg>/Dspp<tm1.1(KOMP)Vlcg>	C57BL/6N-Dspp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705991	M	MP:0008528	polycystic kidney	Dspp<tm1.1(KOMP)Vlcg>/Dspp<tm1.1(KOMP)Vlcg>	C57BL/6N-Dspp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705991	M	MP:0002135	abnormal kidney morphology	Dspp<tm1.1(KOMP)Vlcg>/Dspp<tm1.1(KOMP)Vlcg>	C57BL/6N-Dspp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705991	M	MP:0011110	preweaning lethality, incomplete penetrance	Dspp<tm1.1(KOMP)Vlcg>/Dspp<tm1.1(KOMP)Vlcg>	C57BL/6N-Dspp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705992	F	MP:0002968	increased circulating alkaline phosphatase level	Dynll1<tm1(KOMP)Wtsi>/Dynll1<+>	C57BL/6N-Dynll1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705992	M	MP:0005344	increased circulating bilirubin level	Dynll1<tm1(KOMP)Wtsi>/Dynll1<+>	C57BL/6N-Dynll1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705992	F	MP:0010088	decreased circulating fructosamine level	Dynll1<tm1(KOMP)Wtsi>/Dynll1<+>	C57BL/6N-Dynll1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705992	M	MP:0005560	decreased circulating glucose level	Dynll1<tm1(KOMP)Wtsi>/Dynll1<+>	C57BL/6N-Dynll1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705993	M	MP:0002599	increased mean platelet volume	Dynlrb2<tm1a(KOMP)Wtsi>/Dynlrb2<+>	C57BL/6N-Dynlrb2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705993	F	MP:0013279	increased fasting circulating glucose level	Dynlrb2<tm1a(KOMP)Wtsi>/Dynlrb2<+>	C57BL/6N-Dynlrb2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705993	M	MP:0003960	increased lean body mass	Dynlrb2<tm1a(KOMP)Wtsi>/Dynlrb2<+>	C57BL/6N-Dynlrb2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705993	M	MP:0002833	increased heart weight	Dynlrb2<tm1a(KOMP)Wtsi>/Dynlrb2<+>	C57BL/6N-Dynlrb2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705993	M	MP:0010025	decreased total body fat amount	Dynlrb2<tm1a(KOMP)Wtsi>/Dynlrb2<+>	C57BL/6N-Dynlrb2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705993	M	MP:0001566	increased circulating phosphate level	Dynlrb2<tm1a(KOMP)Wtsi>/Dynlrb2<+>	C57BL/6N-Dynlrb2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705993	M	MP:0010092	increased circulating magnesium level	Dynlrb2<tm1a(KOMP)Wtsi>/Dynlrb2<+>	C57BL/6N-Dynlrb2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705994	M	MP:0001925	male infertility	Dynlrb2<tm1a(KOMP)Wtsi>/Dynlrb2<tm1a(KOMP)Wtsi>	C57BL/6N-Dynlrb2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705995	F	MP:0010052	increased grip strength	Edc4<tm1a(EUCOMM)Wtsi>/Edc4<+>	C57BL/6N-Edc4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5705998	M	MP:0002574	increased vertical activity	Eif4ebp3<tm1.1(KOMP)Vlcg>/Eif4ebp3<tm1.1(KOMP)Vlcg>	C57BL/6N-Eif4ebp3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705998	M	MP:0006203	eye hemorrhage	Eif4ebp3<tm1.1(KOMP)Vlcg>/Eif4ebp3<tm1.1(KOMP)Vlcg>	C57BL/6N-Eif4ebp3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705999	F	MP:0001926	female infertility	Emx1<tm1.1(KOMP)Vlcg>/Emx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Emx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705999	F	MP:0003795	abnormal bone structure	Emx1<tm1.1(KOMP)Vlcg>/Emx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Emx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705999	F	MP:0011110	preweaning lethality, incomplete penetrance	Emx1<tm1.1(KOMP)Vlcg>/Emx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Emx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705999	M	MP:0002175	decreased brain weight	Emx1<tm1.1(KOMP)Vlcg>/Emx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Emx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705999	M	MP:0000266	abnormal heart morphology	Emx1<tm1.1(KOMP)Vlcg>/Emx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Emx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705999	F	MP:0009709	hydrometra	Emx1<tm1.1(KOMP)Vlcg>/Emx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Emx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705999	M	MP:0000274	enlarged heart	Emx1<tm1.1(KOMP)Vlcg>/Emx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Emx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705999	F	MP:0001120	abnormal uterus morphology	Emx1<tm1.1(KOMP)Vlcg>/Emx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Emx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5705999	F	MP:0010053	decreased grip strength	Emx1<tm1.1(KOMP)Vlcg>/Emx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Emx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706000	M	MP:0010123	increased bone mineral content	Erp44<tm1a(KOMP)Wtsi>/Erp44<+>	C57BL/6N-Erp44<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706000	M	MP:0003960	increased lean body mass	Erp44<tm1a(KOMP)Wtsi>/Erp44<+>	C57BL/6N-Erp44<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706002	F	MP:0011100	preweaning lethality, complete penetrance	Exosc3<tm1.1(KOMP)Vlcg>/Exosc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Exosc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706003	F	MP:0011110	preweaning lethality, incomplete penetrance	Fads1<tm1.1(KOMP)Vlcg>/Fads1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fads1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706003	M	MP:0010025	decreased total body fat amount	Fads1<tm1.1(KOMP)Vlcg>/Fads1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fads1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706003	M	MP:0010123	increased bone mineral content	Fads1<tm1.1(KOMP)Vlcg>/Fads1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fads1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706003	M	MP:0003917	increased kidney weight	Fads1<tm1.1(KOMP)Vlcg>/Fads1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fads1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706003	F	MP:0001417	decreased exploration in new environment	Fads1<tm1.1(KOMP)Vlcg>/Fads1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fads1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706003	M	MP:0001147	small testis	Fads1<tm1.1(KOMP)Vlcg>/Fads1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fads1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706003	M	MP:0001258	decreased body length	Fads1<tm1.1(KOMP)Vlcg>/Fads1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fads1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706003	M	MP:0002644	decreased circulating triglyceride level	Fads1<tm1.1(KOMP)Vlcg>/Fads1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fads1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706003	M	MP:0005179	decreased circulating cholesterol level	Fads1<tm1.1(KOMP)Vlcg>/Fads1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fads1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706003	M	MP:0001146	abnormal testis morphology	Fads1<tm1.1(KOMP)Vlcg>/Fads1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fads1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706003	F	MP:0001566	increased circulating phosphate level	Fads1<tm1.1(KOMP)Vlcg>/Fads1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fads1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706003	M	MP:0002176	increased brain weight	Fads1<tm1.1(KOMP)Vlcg>/Fads1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fads1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706005	M	MP:0003020	decreased circulating chloride level	Farsa<tm2a(EUCOMM)Wtsi>/Farsa<+>	C57BL/6N-Farsa<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706005	M	MP:0005634	decreased circulating sodium level	Farsa<tm2a(EUCOMM)Wtsi>/Farsa<+>	C57BL/6N-Farsa<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706005	M	MP:0005293	impaired glucose tolerance	Farsa<tm2a(EUCOMM)Wtsi>/Farsa<+>	C57BL/6N-Farsa<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706005	M	MP:0000221	decreased leukocyte cell number	Farsa<tm2a(EUCOMM)Wtsi>/Farsa<+>	C57BL/6N-Farsa<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706005	F	MP:0002079	increased circulating insulin level	Farsa<tm2a(EUCOMM)Wtsi>/Farsa<+>	C57BL/6N-Farsa<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706005	M	MP:0010124	decreased bone mineral content	Farsa<tm2a(EUCOMM)Wtsi>/Farsa<+>	C57BL/6N-Farsa<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706005	M	MP:0000063	decreased bone mineral density	Farsa<tm2a(EUCOMM)Wtsi>/Farsa<+>	C57BL/6N-Farsa<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706006	F	MP:0010052	increased grip strength	Fbxo47<tm1a(EUCOMM)Wtsi>/Fbxo47<+>	C57BL/6N-Fbxo47<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706008	M	MP:0011110	preweaning lethality, incomplete penetrance	Ffar1<tm1.1(KOMP)Vlcg>/Ffar1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ffar1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706009	F	MP:0010378	increased respiratory quotient	Fgfr1<tm1.1(KOMP)Vlcg>/Fgfr1<+>	C57BL/6N-Fgfr1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706010	M	MP:0011940	decreased food intake	Frrs1<tm1a(EUCOMM)Wtsi>/Frrs1<+>	C57BL/6N-Frrs1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706010	M	MP:0001554	increased circulating free fatty acids level	Frrs1<tm1a(EUCOMM)Wtsi>/Frrs1<+>	C57BL/6N-Frrs1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706013	M	MP:0001925	male infertility	Gga1<tm1.1(KOMP)Vlcg>/Gga1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gga1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706013	M	MP:0001146	abnormal testis morphology	Gga1<tm1.1(KOMP)Vlcg>/Gga1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gga1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706013	M	MP:0001147	small testis	Gga1<tm1.1(KOMP)Vlcg>/Gga1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gga1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706014	M	MP:0003443	increased circulating glycerol level	Glg1<tm1a(KOMP)Wtsi>/Glg1<+>	C57BL/6N-Glg1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706014	M	MP:0001552	increased circulating triglyceride level	Glg1<tm1a(KOMP)Wtsi>/Glg1<+>	C57BL/6N-Glg1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706016	M	MP:0003068	enlarged kidney	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	M	MP:0002135	abnormal kidney morphology	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	M	MP:0001147	small testis	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	M	MP:0005179	decreased circulating cholesterol level	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	M	MP:0003960	increased lean body mass	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	F	MP:0009709	hydrometra	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	M	MP:0000266	abnormal heart morphology	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	M	MP:0002833	increased heart weight	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	M	MP:0011110	preweaning lethality, incomplete penetrance	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	F	MP:0001120	abnormal uterus morphology	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	M	MP:0001146	abnormal testis morphology	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	M	MP:0000274	enlarged heart	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	M	MP:0003917	increased kidney weight	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	M	MP:0010025	decreased total body fat amount	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706016	M	MP:0004952	increased spleen weight	Gpld1<tm1.1(KOMP)Vlcg>/Gpld1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpld1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706019	M	MP:0010024	increased total body fat amount	Gtf2a1<tm1a(KOMP)Wtsi>/Gtf2a1<+>	C57BL/6N-Gtf2a1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706020	M	MP:0000062	increased bone mineral density	Hpcal4<tm1.1(KOMP)Vlcg>/Hpcal4<tm1.1(KOMP)Vlcg>	C57BL/6N-Hpcal4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706020	M	MP:0005631	decreased lung weight	Hpcal4<tm1.1(KOMP)Vlcg>/Hpcal4<tm1.1(KOMP)Vlcg>	C57BL/6N-Hpcal4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706023	M	MP:0010067	increased red blood cell distribution width	Ift80<tm1a(KOMP)Wtsi>/Ift80<+>	C57BL/6N-Ift80<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706024	F	MP:0002546	mydriasis	Jmjd1c<tm1a(EUCOMM)Wtsi>/Jmjd1c<+>	C57BL/6N-Jmjd1c<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706024	F	MP:0001322	abnormal iris morphology	Jmjd1c<tm1a(EUCOMM)Wtsi>/Jmjd1c<+>	C57BL/6N-Jmjd1c<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706025	M	MP:0001513	limb grasping	Kcnj3<tm1.1(KOMP)Vlcg>/Kcnj3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnj3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706025	M	MP:0004924	abnormal behavior	Kcnj3<tm1.1(KOMP)Vlcg>/Kcnj3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnj3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706025	M	MP:0002631	abnormal epididymis morphology	Kcnj3<tm1.1(KOMP)Vlcg>/Kcnj3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnj3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706025	M	MP:0011110	preweaning lethality, incomplete penetrance	Kcnj3<tm1.1(KOMP)Vlcg>/Kcnj3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnj3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706025	M	MP:0010378	increased respiratory quotient	Kcnj3<tm1.1(KOMP)Vlcg>/Kcnj3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnj3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706025	M	MP:0020870	decreased thigmotaxis	Kcnj3<tm1.1(KOMP)Vlcg>/Kcnj3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnj3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706025	M	MP:0004931	enlarged epididymis	Kcnj3<tm1.1(KOMP)Vlcg>/Kcnj3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnj3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706026	M	MP:0005293	impaired glucose tolerance	Kifap3<tm1a(KOMP)Wtsi>/Kifap3<+>	C57BL/6N-Kifap3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706028	F	MP:0003036	vertebral transformation	L3mbtl2<tm2a(EUCOMM)Wtsi>/L3mbtl2<+>	C57BL/6N-L3mbtl2<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706029	M	MP:0002833	increased heart weight	Lama4<tm1.1(KOMP)Vlcg>/Lama4<tm1.1(KOMP)Vlcg>	C57BL/6N-Lama4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706029	M	MP:0011110	preweaning lethality, incomplete penetrance	Lama4<tm1.1(KOMP)Vlcg>/Lama4<tm1.1(KOMP)Vlcg>	C57BL/6N-Lama4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706029	F	MP:0002968	increased circulating alkaline phosphatase level	Lama4<tm1.1(KOMP)Vlcg>/Lama4<tm1.1(KOMP)Vlcg>	C57BL/6N-Lama4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706029	F	MP:0002606	increased basophil cell number	Lama4<tm1.1(KOMP)Vlcg>/Lama4<tm1.1(KOMP)Vlcg>	C57BL/6N-Lama4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706029	F	MP:0002060	abnormal skin morphology	Lama4<tm1.1(KOMP)Vlcg>/Lama4<tm1.1(KOMP)Vlcg>	C57BL/6N-Lama4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706030	M	MP:0010092	increased circulating magnesium level	Lonrf3<tm1a(KOMP)Wtsi>/Y	C57BL/6N-Lonrf3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706030	M	MP:0001554	increased circulating free fatty acids level	Lonrf3<tm1a(KOMP)Wtsi>/Y	C57BL/6N-Lonrf3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706031	M	MP:0005292	improved glucose tolerance	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<+>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706031	M	MP:0003917	increased kidney weight	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<+>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706031	M	MP:0001147	small testis	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<+>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706031	M	MP:0000274	enlarged heart	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<+>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706031	F	MP:0001120	abnormal uterus morphology	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<+>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706031	M	MP:0002060	abnormal skin morphology	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<+>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706031	M	MP:0000598	abnormal liver morphology	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<+>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706031	F	MP:0000689	abnormal spleen morphology	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<+>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706031	F	MP:0004906	enlarged uterus	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<+>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706031	F	MP:0000691	enlarged spleen	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<+>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706031	M	MP:0001146	abnormal testis morphology	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<+>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706031	M	MP:0000266	abnormal heart morphology	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<+>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706031	F	MP:0002098	abnormal vibrissa morphology	Loricrin<tm1.1(KOMP)Vlcg>/Loricrin<+>	C57BL/6N-Loricrin<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706033	F	MP:0005011	increased eosinophil cell number	Lta<tm1.1(KOMP)Vlcg>/Lta<tm1.1(KOMP)Vlcg>	C57BL/6N-Lta<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706034	M	MP:0011939	increased food intake	Lypd3<tm1.1(KOMP)Vlcg>/Lypd3<+>	C57BL/6N-Lypd3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706034	M	MP:0005565	increased blood urea nitrogen level	Lypd3<tm1.1(KOMP)Vlcg>/Lypd3<+>	C57BL/6N-Lypd3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706034	M	MP:0001552	increased circulating triglyceride level	Lypd3<tm1.1(KOMP)Vlcg>/Lypd3<+>	C57BL/6N-Lypd3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706035	M	MP:0010067	increased red blood cell distribution width	Lztr1<tm1a(EUCOMM)Wtsi>/Lztr1<+>	C57BL/6N-Lztr1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706036	M	MP:0013278	decreased fasting circulating glucose level	Map3k1<tm1a(KOMP)Wtsi>/Map3k1<+>	C57BL/6N-Map3k1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706036	M	MP:0003960	increased lean body mass	Map3k1<tm1a(KOMP)Wtsi>/Map3k1<+>	C57BL/6N-Map3k1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706036	M	MP:0010088	decreased circulating fructosamine level	Map3k1<tm1a(KOMP)Wtsi>/Map3k1<+>	C57BL/6N-Map3k1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706036	M	MP:0010123	increased bone mineral content	Map3k1<tm1a(KOMP)Wtsi>/Map3k1<+>	C57BL/6N-Map3k1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706036	F	MP:0001554	increased circulating free fatty acids level	Map3k1<tm1a(KOMP)Wtsi>/Map3k1<+>	C57BL/6N-Map3k1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706036	F	MP:0001325	abnormal retina morphology	Map3k1<tm1a(KOMP)Wtsi>/Map3k1<+>	C57BL/6N-Map3k1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706036	M	MP:0010067	increased red blood cell distribution width	Map3k1<tm1a(KOMP)Wtsi>/Map3k1<+>	C57BL/6N-Map3k1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706037	M	MP:0002574	increased vertical activity	Mcam<tm1.1(KOMP)Wtsi>/Mcam<tm1.1(KOMP)Wtsi>	C57BL/6N-Mcam<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5706042	M	MP:0009142	decreased prepulse inhibition	Mpzl1<tm1.1(KOMP)Vlcg>/Mpzl1<tm1.1(KOMP)Vlcg>	C57BL/6N-Mpzl1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706042	F	MP:0010123	increased bone mineral content	Mpzl1<tm1.1(KOMP)Vlcg>/Mpzl1<tm1.1(KOMP)Vlcg>	C57BL/6N-Mpzl1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706045	M	MP:0009931	abnormal skin appearance	Nek9<tm1a(EUCOMM)Wtsi>/Nek9<+>	C57BL/6N-Nek9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706045	F	MP:0008810	increased circulating iron level	Nek9<tm1a(EUCOMM)Wtsi>/Nek9<+>	C57BL/6N-Nek9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706045	M	MP:0000218	increased leukocyte cell number	Nek9<tm1a(EUCOMM)Wtsi>/Nek9<+>	C57BL/6N-Nek9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706048	M	MP:0010025	decreased total body fat amount	Nhp2<tm1a(KOMP)Wtsi>/Nhp2<+>	C57BL/6N-Nhp2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706048	M	MP:0001257	increased body length	Nhp2<tm1a(KOMP)Wtsi>/Nhp2<+>	C57BL/6N-Nhp2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706048	M	MP:0002599	increased mean platelet volume	Nhp2<tm1a(KOMP)Wtsi>/Nhp2<+>	C57BL/6N-Nhp2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706050	F	MP:0000219	increased neutrophil cell number	Notch3<tm1.1(KOMP)Vlcg>/Notch3<tm1.1(KOMP)Vlcg>	C57BL/6N-Notch3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706050	M	MP:0003917	increased kidney weight	Notch3<tm1.1(KOMP)Vlcg>/Notch3<tm1.1(KOMP)Vlcg>	C57BL/6N-Notch3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706050	M	MP:0010067	increased red blood cell distribution width	Notch3<tm1.1(KOMP)Vlcg>/Notch3<tm1.1(KOMP)Vlcg>	C57BL/6N-Notch3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706050	M	MP:0002135	abnormal kidney morphology	Notch3<tm1.1(KOMP)Vlcg>/Notch3<tm1.1(KOMP)Vlcg>	C57BL/6N-Notch3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706050	M	MP:0003068	enlarged kidney	Notch3<tm1.1(KOMP)Vlcg>/Notch3<tm1.1(KOMP)Vlcg>	C57BL/6N-Notch3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706050	M	MP:0000266	abnormal heart morphology	Notch3<tm1.1(KOMP)Vlcg>/Notch3<tm1.1(KOMP)Vlcg>	C57BL/6N-Notch3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706050	M	MP:0004952	increased spleen weight	Notch3<tm1.1(KOMP)Vlcg>/Notch3<tm1.1(KOMP)Vlcg>	C57BL/6N-Notch3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706050	M	MP:0003402	decreased liver weight	Notch3<tm1.1(KOMP)Vlcg>/Notch3<tm1.1(KOMP)Vlcg>	C57BL/6N-Notch3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706050	M	MP:0000274	enlarged heart	Notch3<tm1.1(KOMP)Vlcg>/Notch3<tm1.1(KOMP)Vlcg>	C57BL/6N-Notch3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706050	M	MP:0005292	improved glucose tolerance	Notch3<tm1.1(KOMP)Vlcg>/Notch3<tm1.1(KOMP)Vlcg>	C57BL/6N-Notch3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706050	M	MP:0002833	increased heart weight	Notch3<tm1.1(KOMP)Vlcg>/Notch3<tm1.1(KOMP)Vlcg>	C57BL/6N-Notch3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706051	M	MP:0010123	increased bone mineral content	Nrde2<tm2a(KOMP)Wtsi>/Nrde2<+>	C57BL/6N-Nrde2<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706051	F	MP:0013279	increased fasting circulating glucose level	Nrde2<tm2a(KOMP)Wtsi>/Nrde2<+>	C57BL/6N-Nrde2<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706052	M	MP:0002135	abnormal kidney morphology	Cimap1d<tm1.1(KOMP)Vlcg>/Cimap1d<+>	C57BL/6N-Cimap1d<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706052	M	MP:0001410	head bobbing	Cimap1d<tm1.1(KOMP)Vlcg>/Cimap1d<+>	C57BL/6N-Cimap1d<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706052	M	MP:0001523	impaired righting response	Cimap1d<tm1.1(KOMP)Vlcg>/Cimap1d<+>	C57BL/6N-Cimap1d<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706052	M	MP:0001406	abnormal gait	Cimap1d<tm1.1(KOMP)Vlcg>/Cimap1d<+>	C57BL/6N-Cimap1d<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706052	M	MP:0000274	enlarged heart	Cimap1d<tm1.1(KOMP)Vlcg>/Cimap1d<+>	C57BL/6N-Cimap1d<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706052	F	MP:0001284	absent vibrissae	Cimap1d<tm1.1(KOMP)Vlcg>/Cimap1d<+>	C57BL/6N-Cimap1d<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706052	M	MP:0000266	abnormal heart morphology	Cimap1d<tm1.1(KOMP)Vlcg>/Cimap1d<+>	C57BL/6N-Cimap1d<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706052	M	MP:0003068	enlarged kidney	Cimap1d<tm1.1(KOMP)Vlcg>/Cimap1d<+>	C57BL/6N-Cimap1d<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706053	M	MP:0010025	decreased total body fat amount	Ogdh<tm1e(KOMP)Wtsi>/Ogdh<+>	C57BL/6N-Ogdh<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706053	F	MP:0002874	decreased hemoglobin content	Ogdh<tm1e(KOMP)Wtsi>/Ogdh<+>	C57BL/6N-Ogdh<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706053	M	MP:0003960	increased lean body mass	Ogdh<tm1e(KOMP)Wtsi>/Ogdh<+>	C57BL/6N-Ogdh<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706053	F	MP:0002875	decreased erythrocyte cell number	Ogdh<tm1e(KOMP)Wtsi>/Ogdh<+>	C57BL/6N-Ogdh<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706053	M	MP:0010052	increased grip strength	Ogdh<tm1e(KOMP)Wtsi>/Ogdh<+>	C57BL/6N-Ogdh<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706053	F	MP:0000208	decreased hematocrit	Ogdh<tm1e(KOMP)Wtsi>/Ogdh<+>	C57BL/6N-Ogdh<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706057	F	MP:0011110	preweaning lethality, incomplete penetrance	Panx3<tm1b(KOMP)Wtsi>/Panx3<tm1b(KOMP)Wtsi>	C57BL/6N-Panx3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5706059	M	MP:0001147	small testis	Pdk1<tm1.1(KOMP)Vlcg>/Pdk1<tm1.1(KOMP)Vlcg>	C57BL/6N-Pdk1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706059	M	MP:0001146	abnormal testis morphology	Pdk1<tm1.1(KOMP)Vlcg>/Pdk1<tm1.1(KOMP)Vlcg>	C57BL/6N-Pdk1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706060	M	MP:0001312	abnormal cornea morphology	Pfn1<tm1a(EUCOMM)Wtsi>/Pfn1<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Pfn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706060	F	MP:0010092	increased circulating magnesium level	Pfn1<tm1a(EUCOMM)Wtsi>/Pfn1<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Pfn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706060	F	MP:0010025	decreased total body fat amount	Pfn1<tm1a(EUCOMM)Wtsi>/Pfn1<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Pfn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5706060	F	MP:0010088	decreased circulating fructosamine level	Pfn1<tm1a(EUCOMM)Wtsi>/Pfn1<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Pfn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5706060	F	MP:0001307	fused cornea and lens	Pfn1<tm1a(EUCOMM)Wtsi>/Pfn1<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Pfn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706060	M	MP:0005292	improved glucose tolerance	Pfn1<tm1a(EUCOMM)Wtsi>/Pfn1<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Pfn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706060	F	MP:0010124	decreased bone mineral content	Pfn1<tm1a(EUCOMM)Wtsi>/Pfn1<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Pfn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5706060	M	MP:0008806	increased circulating amylase level	Pfn1<tm1a(EUCOMM)Wtsi>/Pfn1<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Pfn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706062	F	MP:0010124	decreased bone mineral content	Pigf<tm1a(KOMP)Wtsi>/Pigf<+>	C57BL/6N-Pigf<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706062	F	MP:0003961	decreased lean body mass	Pigf<tm1a(KOMP)Wtsi>/Pigf<+>	C57BL/6N-Pigf<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706062	F	MP:0010024	increased total body fat amount	Pigf<tm1a(KOMP)Wtsi>/Pigf<+>	C57BL/6N-Pigf<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706064	M	MP:0001566	increased circulating phosphate level	Pls3<tm1a(EUCOMM)Wtsi>/Y	C57BL/6N-Pls3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706064	M	MP:0001552	increased circulating triglyceride level	Pls3<tm1a(EUCOMM)Wtsi>/Y	C57BL/6N-Pls3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706064	M	MP:0010052	increased grip strength	Pls3<tm1a(EUCOMM)Wtsi>/Y	C57BL/6N-Pls3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706071	F	MP:0010124	decreased bone mineral content	Pth1r<tm1a(EUCOMM)Hmgu>/Pth1r<+>	C57BL/6N-Pth1r<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:5706071	F	MP:0010024	increased total body fat amount	Pth1r<tm1a(EUCOMM)Hmgu>/Pth1r<+>	C57BL/6N-Pth1r<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:5706071	F	MP:0003961	decreased lean body mass	Pth1r<tm1a(EUCOMM)Hmgu>/Pth1r<+>	C57BL/6N-Pth1r<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:5706072	F	MP:0005565	increased blood urea nitrogen level	Pthlh<tm1a(KOMP)Wtsi>/Pthlh<+>	C57BL/6N-Pthlh<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706074	M	MP:0005179	decreased circulating cholesterol level	Rab5c<tm1a(EUCOMM)Wtsi>/Rab5c<+>	C57BL/6N-Rab5c<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706074	F	MP:0002968	increased circulating alkaline phosphatase level	Rab5c<tm1a(EUCOMM)Wtsi>/Rab5c<+>	C57BL/6N-Rab5c<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706074	F	MP:0005568	increased circulating total protein level	Rab5c<tm1a(EUCOMM)Wtsi>/Rab5c<+>	C57BL/6N-Rab5c<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706074	F	MP:0010087	increased circulating fructosamine level	Rab5c<tm1a(EUCOMM)Wtsi>/Rab5c<+>	C57BL/6N-Rab5c<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706075	F	MP:0005628	decreased circulating potassium level	Ralgapb<tm1a(KOMP)Wtsi>/Ralgapb<+>	C57BL/6N-Ralgapb<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706076	M	MP:0000266	abnormal heart morphology	Rasd1<tm1.1(KOMP)Vlcg>/Rasd1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rasd1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706076	M	MP:0000274	enlarged heart	Rasd1<tm1.1(KOMP)Vlcg>/Rasd1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rasd1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706077	F	MP:0011100	preweaning lethality, complete penetrance	Rassf8<tm1.1(KOMP)Vlcg>/Rassf8<tm1.1(KOMP)Vlcg>	C57BL/6N-Rassf8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706079	F	MP:0000367	abnormal coat/ hair morphology	Recql4<tm1.1(KOMP)Vlcg>/Recql4<+>	C57BL/6N-Recql4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706079	M	MP:0005655	increased aggression	Recql4<tm1.1(KOMP)Vlcg>/Recql4<+>	C57BL/6N-Recql4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706080	F	MP:0001120	abnormal uterus morphology	Rfx6<tm1.1(KOMP)Vlcg>/Rfx6<+>	C57BL/6N-Rfx6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706080	F	MP:0009709	hydrometra	Rfx6<tm1.1(KOMP)Vlcg>/Rfx6<+>	C57BL/6N-Rfx6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706081	F	MP:0002060	abnormal skin morphology	Rhbdl1<tm1.1(KOMP)Vlcg>/Rhbdl1<+>	C57BL/6N-Rhbdl1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706081	M	MP:0005343	increased circulating aspartate transaminase level	Rhbdl1<tm1.1(KOMP)Vlcg>/Rhbdl1<+>	C57BL/6N-Rhbdl1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706081	M	MP:0005344	increased circulating bilirubin level	Rhbdl1<tm1.1(KOMP)Vlcg>/Rhbdl1<+>	C57BL/6N-Rhbdl1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706082	F	MP:0004509	abnormal pelvic girdle bone morphology	Rnaseh2c<tm1(KOMP)Wtsi>/Rnaseh2c<+>	C57BL/6N-Rnaseh2c<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706085	M	MP:0000221	decreased leukocyte cell number	Sap130<tm1a(KOMP)Mbp>/Sap130<+>	C57BL/6N-Sap130<tm1a(KOMP)Mbp>/Wtsi	N	MGI:5576271
MGI:5706085	M	MP:0011939	increased food intake	Sap130<tm1a(KOMP)Mbp>/Sap130<+>	C57BL/6N-Sap130<tm1a(KOMP)Mbp>/Wtsi	N	MGI:5576271
MGI:5706087	F	MP:0010052	increased grip strength	Septin10<tm1a(KOMP)Wtsi>/Septin10<+>	C57BL/6N-Septin10<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706088	F	MP:0006358	absent pinna reflex	Setd5<tm1a(EUCOMM)Wtsi>/Setd5<+>	C57BL/6N-Setd5<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706088	F	MP:0004973	increased regulatory T cell number	Setd5<tm1a(EUCOMM)Wtsi>/Setd5<+>	C57BL/6N-Setd5<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706088	M	MP:0002100	abnormal tooth morphology	Setd5<tm1a(EUCOMM)Wtsi>/Setd5<+>	C57BL/6N-Setd5<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706088	M	MP:0000438	abnormal cranium morphology	Setd5<tm1a(EUCOMM)Wtsi>/Setd5<+>	C57BL/6N-Setd5<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706088	F	MP:0000220	increased monocyte cell number	Setd5<tm1a(EUCOMM)Wtsi>/Setd5<+>	C57BL/6N-Setd5<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706088	M	MP:0004609	vertebral fusion	Setd5<tm1a(EUCOMM)Wtsi>/Setd5<+>	C57BL/6N-Setd5<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706088	M	MP:0000443	abnormal snout morphology	Setd5<tm1a(EUCOMM)Wtsi>/Setd5<+>	C57BL/6N-Setd5<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706088	F	MP:0002075	abnormal coat/hair pigmentation	Setd5<tm1a(EUCOMM)Wtsi>/Setd5<+>	C57BL/6N-Setd5<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706088	M	MP:0000455	abnormal maxilla morphology	Setd5<tm1a(EUCOMM)Wtsi>/Setd5<+>	C57BL/6N-Setd5<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706090	M	MP:0002874	decreased hemoglobin content	Skida1<tm1(KOMP)Wtsi>/Skida1<+>	C57BL/6N-Skida1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706090	M	MP:0005561	increased mean corpuscular hemoglobin	Skida1<tm1(KOMP)Wtsi>/Skida1<+>	C57BL/6N-Skida1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706090	F	MP:0005477	increased circulating thyroxine level	Skida1<tm1(KOMP)Wtsi>/Skida1<+>	C57BL/6N-Skida1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706090	F	MP:0004599	abnormal vertebral arch morphology	Skida1<tm1(KOMP)Wtsi>/Skida1<+>	C57BL/6N-Skida1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706090	M	MP:0002875	decreased erythrocyte cell number	Skida1<tm1(KOMP)Wtsi>/Skida1<+>	C57BL/6N-Skida1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706090	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Skida1<tm1(KOMP)Wtsi>/Skida1<+>	C57BL/6N-Skida1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706090	M	MP:0000208	decreased hematocrit	Skida1<tm1(KOMP)Wtsi>/Skida1<+>	C57BL/6N-Skida1<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706091	M	MP:0010052	increased grip strength	Slc20a2<tm1a(EUCOMM)Wtsi>/Slc20a2<+>	C57BL/6N-Slc20a2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706094	M	MP:0005419	decreased circulating serum albumin level	Slc39a5<tm1b(KOMP)Wtsi>/Slc39a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc39a5<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5706094	F	MP:0002968	increased circulating alkaline phosphatase level	Slc39a5<tm1b(KOMP)Wtsi>/Slc39a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc39a5<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5706094	M	MP:0000062	increased bone mineral density	Slc39a5<tm1b(KOMP)Wtsi>/Slc39a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc39a5<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5706096	M	MP:0010025	decreased total body fat amount	Slc5a7<tm1a(KOMP)Wtsi>/Slc5a7<+>	C57BL/6N-Slc5a7<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706096	M	MP:0010088	decreased circulating fructosamine level	Slc5a7<tm1a(KOMP)Wtsi>/Slc5a7<+>	C57BL/6N-Slc5a7<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706096	M	MP:0002073	abnormal hair growth	Slc5a7<tm1a(KOMP)Wtsi>/Slc5a7<+>	C57BL/6N-Slc5a7<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706101	F	MP:0011110	preweaning lethality, incomplete penetrance	Spef1<tm1.1(KOMP)Vlcg>/Spef1<tm1.1(KOMP)Vlcg>	C57BL/6N-Spef1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706102	M	MP:0000494	abnormal cecum morphology	Srpk3<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Srpk3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5706102	M	MP:0002731	megacolon	Srpk3<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Srpk3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5706102	M	MP:0010053	decreased grip strength	Srpk3<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Srpk3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5706102	M	MP:0000220	increased monocyte cell number	Srpk3<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Srpk3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5706102	M	MP:0000063	decreased bone mineral density	Srpk3<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Srpk3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5706104	F	MP:0000367	abnormal coat/ hair morphology	Stxbp5l<tm1.1(KOMP)Vlcg>/Stxbp5l<tm1.1(KOMP)Vlcg>	C57BL/6N-Stxbp5l<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706104	M	MP:0002574	increased vertical activity	Stxbp5l<tm1.1(KOMP)Vlcg>/Stxbp5l<tm1.1(KOMP)Vlcg>	C57BL/6N-Stxbp5l<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706104	F	MP:0010123	increased bone mineral content	Stxbp5l<tm1.1(KOMP)Vlcg>/Stxbp5l<tm1.1(KOMP)Vlcg>	C57BL/6N-Stxbp5l<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706104	F	MP:0002968	increased circulating alkaline phosphatase level	Stxbp5l<tm1.1(KOMP)Vlcg>/Stxbp5l<tm1.1(KOMP)Vlcg>	C57BL/6N-Stxbp5l<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706105	F	MP:0003036	vertebral transformation	Supt5<tm2a(KOMP)Wtsi>/Supt5<+>	C57BL/6N-Supt5<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706106	F	MP:0003961	decreased lean body mass	Syt1<tm1a(EUCOMM)Wtsi>/Syt1<+>	C57BL/6N-Syt1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706106	F	MP:0010124	decreased bone mineral content	Syt1<tm1a(EUCOMM)Wtsi>/Syt1<+>	C57BL/6N-Syt1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706107	F	MP:0001325	abnormal retina morphology	Tcf4<tm1a(EUCOMM)Wtsi>/Tcf4<+>	C57BL/6N-Tcf4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706108	M	MP:0000062	increased bone mineral density	Tcf7l2<tm1a(EUCOMM)Wtsi>/Tcf7l2<+>	C57BL/6N-Tcf7l2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706108	M	MP:0002599	increased mean platelet volume	Tcf7l2<tm1a(EUCOMM)Wtsi>/Tcf7l2<+>	C57BL/6N-Tcf7l2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706108	M	MP:0010067	increased red blood cell distribution width	Tcf7l2<tm1a(EUCOMM)Wtsi>/Tcf7l2<+>	C57BL/6N-Tcf7l2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706108	M	MP:0010123	increased bone mineral content	Tcf7l2<tm1a(EUCOMM)Wtsi>/Tcf7l2<+>	C57BL/6N-Tcf7l2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706113	F	MP:0002092	abnormal eye morphology	Tmem30b<tm1b(EUCOMM)Wtsi>/Tmem30b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem30b<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5706113	F	MP:0000274	enlarged heart	Tmem30b<tm1b(EUCOMM)Wtsi>/Tmem30b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem30b<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5706113	M	MP:0000538	abnormal urinary bladder morphology	Tmem30b<tm1b(EUCOMM)Wtsi>/Tmem30b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem30b<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5706115	M	MP:0010052	increased grip strength	Traf6<tm2a(EUCOMM)Wtsi>/Traf6<+>	C57BL/6N-Traf6<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706117	F	MP:0001325	abnormal retina morphology	Tsfm<tm1a(EUCOMM)Wtsi>/Tsfm<+>	C57BL/6N-Tsfm<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706118	M	MP:0000274	enlarged heart	Txndc5<tm1.1(KOMP)Vlcg>/Txndc5<+>	C57BL/6N-Txndc5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706118	M	MP:0001146	abnormal testis morphology	Txndc5<tm1.1(KOMP)Vlcg>/Txndc5<+>	C57BL/6N-Txndc5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706118	M	MP:0001147	small testis	Txndc5<tm1.1(KOMP)Vlcg>/Txndc5<+>	C57BL/6N-Txndc5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706118	M	MP:0002079	increased circulating insulin level	Txndc5<tm1.1(KOMP)Vlcg>/Txndc5<+>	C57BL/6N-Txndc5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706118	M	MP:0000266	abnormal heart morphology	Txndc5<tm1.1(KOMP)Vlcg>/Txndc5<+>	C57BL/6N-Txndc5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706118	M	MP:0001157	small seminal vesicle	Txndc5<tm1.1(KOMP)Vlcg>/Txndc5<+>	C57BL/6N-Txndc5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706118	M	MP:0002644	decreased circulating triglyceride level	Txndc5<tm1.1(KOMP)Vlcg>/Txndc5<+>	C57BL/6N-Txndc5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706118	M	MP:0002059	abnormal seminal vesicle morphology	Txndc5<tm1.1(KOMP)Vlcg>/Txndc5<+>	C57BL/6N-Txndc5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706118	M	MP:0005179	decreased circulating cholesterol level	Txndc5<tm1.1(KOMP)Vlcg>/Txndc5<+>	C57BL/6N-Txndc5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706119	F	MP:0000745	tremors	Ublcp1<tm1b(KOMP)Wtsi>/Ublcp1<+>	C57BL/6N-Ublcp1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5706120	M	MP:0000182	increased circulating LDL cholesterol level	Usp11<tm1(KOMP)Wtsi>/Y	C57BL/6N-Usp11<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706120	M	MP:0001556	increased circulating HDL cholesterol level	Usp11<tm1(KOMP)Wtsi>/Y	C57BL/6N-Usp11<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706121	F	MP:0005561	increased mean corpuscular hemoglobin	Usp22<tm1a(KOMP)Wtsi>/Usp22<+>	C57BL/6N-Usp22<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706121	M	MP:0010067	increased red blood cell distribution width	Usp22<tm1a(KOMP)Wtsi>/Usp22<+>	C57BL/6N-Usp22<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706121	M	MP:0003960	increased lean body mass	Usp22<tm1a(KOMP)Wtsi>/Usp22<+>	C57BL/6N-Usp22<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706121	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Usp22<tm1a(KOMP)Wtsi>/Usp22<+>	C57BL/6N-Usp22<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706123	M	MP:0010099	abnormal thoracic cage shape	Vps33b<tm1a(EUCOMM)Wtsi>/Vps33b<+>	C57BL/6N-Vps33b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706123	M	MP:0001556	increased circulating HDL cholesterol level	Vps33b<tm1a(EUCOMM)Wtsi>/Vps33b<+>	C57BL/6N-Vps33b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706124	F	MP:0010052	increased grip strength	Vps51<tm1a(KOMP)Wtsi>/Vps51<+>	C57BL/6N-Vps51<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706124	M	MP:0005344	increased circulating bilirubin level	Vps51<tm1a(KOMP)Wtsi>/Vps51<+>	C57BL/6N-Vps51<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706127	M	MP:0010053	decreased grip strength	Galnt17<tm1.1(KOMP)Vlcg>/Galnt17<tm1.1(KOMP)Vlcg>	C57BL/6N-Galnt17<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5706128	F	MP:0001417	decreased exploration in new environment	Zbed4<tm1.1(KOMP)Mbp>/Zbed4<+>	C57BL/6N-Zbed4<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5706128	M	MP:0002135	abnormal kidney morphology	Zbed4<tm1.1(KOMP)Mbp>/Zbed4<+>	C57BL/6N-Zbed4<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5706128	M	MP:0000274	enlarged heart	Zbed4<tm1.1(KOMP)Mbp>/Zbed4<+>	C57BL/6N-Zbed4<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5706128	M	MP:0000266	abnormal heart morphology	Zbed4<tm1.1(KOMP)Mbp>/Zbed4<+>	C57BL/6N-Zbed4<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5706128	M	MP:0000689	abnormal spleen morphology	Zbed4<tm1.1(KOMP)Mbp>/Zbed4<+>	C57BL/6N-Zbed4<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5706128	M	MP:0003068	enlarged kidney	Zbed4<tm1.1(KOMP)Mbp>/Zbed4<+>	C57BL/6N-Zbed4<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5706128	M	MP:0000691	enlarged spleen	Zbed4<tm1.1(KOMP)Mbp>/Zbed4<+>	C57BL/6N-Zbed4<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5706130	M	MP:0001304	cataract	Zfp182<tm1a(KOMP)Wtsi>/Y	C57BL/6N-Zfp182<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706130	M	MP:0001303	abnormal lens morphology	Zfp182<tm1a(KOMP)Wtsi>/Y	C57BL/6N-Zfp182<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5706723	F	MP:0020011	increased bone mineral density of femur	Tg(Col1a1-TK*)#Rowe/0	involves: CD-1	N	25111968
MGI:5706723	F	MP:0004993	decreased bone resorption	Tg(Col1a1-TK*)#Rowe/0	involves: CD-1	N	25111968
MGI:5706723	F	MP:0004985	decreased osteoclast cell number	Tg(Col1a1-TK*)#Rowe/0	involves: CD-1	N	25111968
MGI:5706723	F	MP:0010868	increased bone trabecula number	Tg(Col1a1-TK*)#Rowe/0	involves: CD-1	N	25111968
MGI:5706723	F	MP:0013617	increased areal bone mineral density	Tg(Col1a1-TK*)#Rowe/0	involves: CD-1	N	25111968
MGI:5706723	F	MP:0013641	increased vertebra stiffness	Tg(Col1a1-TK*)#Rowe/0	involves: CD-1	N	25111968
MGI:5706723	F	MP:0008271	abnormal bone ossification	Tg(Col1a1-TK*)#Rowe/0	involves: CD-1	N	25111968
MGI:5706723	F	MP:0002896	abnormal bone mineralization	Tg(Col1a1-TK*)#Rowe/0	involves: CD-1	N	25111968
MGI:5706723	F	MP:0001542	abnormal bone strength	Tg(Col1a1-TK*)#Rowe/0	involves: CD-1	N	25111968
MGI:5706723	F	MP:0000062	increased bone mineral density	Tg(Col1a1-TK*)#Rowe/0	involves: CD-1	N	25111968
MGI:5706723	F	MP:0009347	increased trabecular bone thickness	Tg(Col1a1-TK*)#Rowe/0	involves: CD-1	N	25111968
MGI:5706723	F	MP:0010878	increased trabecular bone volume	Tg(Col1a1-TK*)#Rowe/0	involves: CD-1	N	25111968
MGI:5706792	M	MP:0009402	decreased skeletal muscle fiber diameter	Fhl1<tm1.1Mihi>/Y	involves: 129S/SvEv * C57BL/6J * C57BL/6NJ	N	25274776
MGI:5706792	M	MP:0010053	decreased grip strength	Fhl1<tm1.1Mihi>/Y	involves: 129S/SvEv * C57BL/6J * C57BL/6NJ	N	25274776
MGI:5706792	M	MP:0012106	impaired exercise endurance	Fhl1<tm1.1Mihi>/Y	involves: 129S/SvEv * C57BL/6J * C57BL/6NJ	N	25274776
MGI:5706792	M	MP:0009404	centrally nucleated skeletal muscle fibers	Fhl1<tm1.1Mihi>/Y	involves: 129S/SvEv * C57BL/6J * C57BL/6NJ	N	25274776
MGI:5706792	M	MP:0000751	myopathy	Fhl1<tm1.1Mihi>/Y	involves: 129S/SvEv * C57BL/6J * C57BL/6NJ	N	25274776
MGI:5706792	M	MP:0001262	decreased body weight	Fhl1<tm1.1Mihi>/Y	involves: 129S/SvEv * C57BL/6J * C57BL/6NJ	N	25274776
MGI:5706798	M	MP:0001925	male infertility	E2f4<tm2.1Lees>/E2f4<tm2.1Lees>,E2f5<tm1Dli>/E2f5<+>,Tg(Vil1-cre)20Syr/0	involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2	N	26825228
MGI:5706798	M	MP:0006423	dilated rete testis	E2f4<tm2.1Lees>/E2f4<tm2.1Lees>,E2f5<tm1Dli>/E2f5<+>,Tg(Vil1-cre)20Syr/0	involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2	N	26825228
MGI:5706798	M	MP:0004728	abnormal efferent ductules of testis morphology	E2f4<tm2.1Lees>/E2f4<tm2.1Lees>,E2f5<tm1Dli>/E2f5<+>,Tg(Vil1-cre)20Syr/0	involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2	N	26825228
MGI:5706798	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	E2f4<tm2.1Lees>/E2f4<tm2.1Lees>,E2f5<tm1Dli>/E2f5<+>,Tg(Vil1-cre)20Syr/0	involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2	N	26825228
MGI:5706798	M	MP:0009257	dilated seminiferous tubule	E2f4<tm2.1Lees>/E2f4<tm2.1Lees>,E2f5<tm1Dli>/E2f5<+>,Tg(Vil1-cre)20Syr/0	involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2	N	26825228
MGI:5706798	M	MP:0002631	abnormal epididymis morphology	E2f4<tm2.1Lees>/E2f4<tm2.1Lees>,E2f5<tm1Dli>/E2f5<+>,Tg(Vil1-cre)20Syr/0	involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2	N	26825228
MGI:5706798	M	MP:0005389	reproductive system phenotype	E2f4<tm2.1Lees>/E2f4<tm2.1Lees>,E2f5<tm1Dli>/E2f5<+>,Tg(Vil1-cre)20Syr/0	involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2	Y	26825228
MGI:5706799	M	MP:0009257	dilated seminiferous tubule	E2f5<tm1Dli>/E2f5<tm1Dli>	involves: 129S1/Sv	N	26825228
MGI:5706799	M	MP:0006423	dilated rete testis	E2f5<tm1Dli>/E2f5<tm1Dli>	involves: 129S1/Sv	N	26825228
MGI:5706800	M	MP:0006423	dilated rete testis	E2f4<tm2.1Lees>/E2f4<tm2.1Lees>,E2f5<tm1Dli>/E2f5<tm1Dli>	involves: 129S1/Sv * 129S4/SvJae * C57BL/6	N	26825228
MGI:5706800	M	MP:0004728	abnormal efferent ductules of testis morphology	E2f4<tm2.1Lees>/E2f4<tm2.1Lees>,E2f5<tm1Dli>/E2f5<tm1Dli>	involves: 129S1/Sv * 129S4/SvJae * C57BL/6	N	26825228
MGI:5706801	M	MP:0006423	dilated rete testis	E2f4<tm2.1Lees>/E2f4<+>,E2f5<tm1Dli>/E2f5<tm1Dli>	involves: 129S1/Sv * 129S4/SvJae * C57BL/6	N	26825228
MGI:5706801	M	MP:0004728	abnormal efferent ductules of testis morphology	E2f4<tm2.1Lees>/E2f4<+>,E2f5<tm1Dli>/E2f5<tm1Dli>	involves: 129S1/Sv * 129S4/SvJae * C57BL/6	N	26825228
MGI:5706802	M	MP:0009257	dilated seminiferous tubule	E2f4<tm1Lees>/E2f4<+>,E2f5<tm1Dli>/E2f5<tm1Dli>	involves: 129S1/Sv * 129S4/SvJae * C57BL/6	N	26825228
MGI:5706939	M	MP:0003331	increased hepatocellular carcinoma incidence	Tg(IRS1)1Mhep/0,Tg(SERPINA1-HBVX)1655Jtsb/0	involves: C3H * C57BL/6 * FVB * ICR	N	26433160
MGI:5707290	F	MP:0004047	abnormal milk composition	Afap1<tm1.2Ycho>/Afap1<tm1.2Ycho>	involves: BALB/cJ * C57BL/6J	N	25043309
MGI:5707290	F	MP:0009506	abnormal mammary gland alveolus morphology	Afap1<tm1.2Ycho>/Afap1<tm1.2Ycho>	involves: BALB/cJ * C57BL/6J	N	25043309
MGI:5707290	F	MP:0001882	abnormal lactation	Afap1<tm1.2Ycho>/Afap1<tm1.2Ycho>	involves: BALB/cJ * C57BL/6J	N	25043309
MGI:5707290	F	MP:0003718	maternal effect	Afap1<tm1.2Ycho>/Afap1<tm1.2Ycho>	involves: BALB/cJ * C57BL/6J	N	25043309
MGI:5707290	F	MP:0006271	abnormal involution of the mammary gland	Afap1<tm1.2Ycho>/Afap1<tm1.2Ycho>	involves: BALB/cJ * C57BL/6J	N	25043309
MGI:5707290	F	MP:0001382	abnormal nursing	Afap1<tm1.2Ycho>/Afap1<tm1.2Ycho>	involves: BALB/cJ * C57BL/6J	N	25043309
MGI:5707295	M	MP:0012320	abnormal body fat mass	Tg(Alb-MYLIP*)1Pton/?	involves: C57BL/6J	N	24935961
MGI:5707295	M	MP:0001552	increased circulating triglyceride level	Tg(Alb-MYLIP*)1Pton/?	involves: C57BL/6J	N	24935961
MGI:5707295	M	MP:0002644	decreased circulating triglyceride level	Tg(Alb-MYLIP*)1Pton/?	involves: C57BL/6J	N	24935961
MGI:5707296	F	MP:0005338	atherosclerotic lesions	Tg(APOE_i3*,APOC1)2Lmh/?	involves: C57BL/6J * CBA	N	24935961
MGI:5707296	F	MP:0000182	increased circulating LDL cholesterol level	Tg(APOE_i3*,APOC1)2Lmh/?	involves: C57BL/6J * CBA	N	24935961
MGI:5707296	F	MP:0005178	increased circulating cholesterol level	Tg(APOE_i3*,APOC1)2Lmh/?	involves: C57BL/6J * CBA	N	24935961
MGI:5707296	F	MP:0001552	increased circulating triglyceride level	Tg(APOE_i3*,APOC1)2Lmh/?	involves: C57BL/6J * CBA	N	24935961
MGI:5707296	F	MP:0005339	increased susceptibility to atherosclerosis	Tg(APOE_i3*,APOC1)2Lmh/?	involves: C57BL/6J * CBA	N	24935961
MGI:5707296	F	MP:0005145	increased circulating VLDL cholesterol level	Tg(APOE_i3*,APOC1)2Lmh/?	involves: C57BL/6J * CBA	N	24935961
MGI:5707333	M	MP:0003960	increased lean body mass	Mc4r<tm1.1Fbz>/Mc4r<tm1.1Fbz>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac	N	21969101
MGI:5707686	M	MP:0000195	decreased circulating calcium level	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	F	MP:0002834	decreased heart weight	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	F	MP:0010124	decreased bone mineral content	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	M	MP:0005534	decreased body temperature	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	M	MP:0002665	decreased circulating corticosterone level	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	M	MP:0003921	abnormal heart left ventricle morphology	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	F	MP:0031391	increased locomotor activity	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	F	MP:0001488	increased startle reflex	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	F	MP:0001262	decreased body weight	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	F	MP:0011971	increased circulating lactate dehydrogenase level	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	M	MP:0009141	increased prepulse inhibition	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	F	MP:0003718	maternal effect	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	F	MP:0004953	decreased spleen weight	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	F	MP:0002764	short tibia	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	F	MP:0002090	abnormal vision	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	F	MP:0004016	decreased bone mass	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	F	MP:0001923	reduced female fertility	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	M	MP:0002981	increased liver weight	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	M	MP:0005574	decreased pulmonary respiratory rate	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707686	M	MP:0001402	decreased locomotor activity	Zscan10<Gt(285B6)1.1Cmhd>/Zscan10<Gt(285B6)1.1Cmhd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	25111779
MGI:5707838	M	MP:0001147	small testis	Dmrtb1<tm1.1Zark>/Dmrtb1<tm1.1Zark>	involves: 129S1/Sv * C57BL/6	N	25249458
MGI:5707838	M	MP:0002216	abnormal seminiferous tubule morphology	Dmrtb1<tm1.1Zark>/Dmrtb1<tm1.1Zark>	involves: 129S1/Sv * C57BL/6	N	25249458
MGI:5707838	M	MP:0002631	abnormal epididymis morphology	Dmrtb1<tm1.1Zark>/Dmrtb1<tm1.1Zark>	involves: 129S1/Sv * C57BL/6	N	25249458
MGI:5707838	M	MP:0008280	abnormal male germ cell apoptosis	Dmrtb1<tm1.1Zark>/Dmrtb1<tm1.1Zark>	involves: 129S1/Sv * C57BL/6	N	25249458
MGI:5707838	M	MP:0001146	abnormal testis morphology	Dmrtb1<tm1.1Zark>/Dmrtb1<tm1.1Zark>	involves: 129S1/Sv * C57BL/6	N	25249458
MGI:5707838	M	MP:0001155	arrest of spermatogenesis	Dmrtb1<tm1.1Zark>/Dmrtb1<tm1.1Zark>	involves: 129S1/Sv * C57BL/6	N	25249458
MGI:5707840	M	MP:0008261	arrest of male meiosis	Dmrtb1<tm1.1Zark>/Dmrtb1<tm1.1Zark>	involves: 129S1/Sv	N	25249458
MGI:5707840	M	MP:0005389	reproductive system phenotype	Dmrtb1<tm1.1Zark>/Dmrtb1<tm1.1Zark>	involves: 129S1/Sv	Y	25249458
MGI:5707840	M	MP:0009452	abnormal synaptonemal complex	Dmrtb1<tm1.1Zark>/Dmrtb1<tm1.1Zark>	involves: 129S1/Sv	N	25249458
MGI:5707840	M	MP:0005169	abnormal male meiosis	Dmrtb1<tm1.1Zark>/Dmrtb1<tm1.1Zark>	involves: 129S1/Sv	N	25249458
MGI:5707924	M	MP:0009234	absent sperm head	Ube2j1<tm1.2Hpl>/Ube2j1<tm1.2Hpl>	involves: BALB/cJ * C57BL/6 * C57BL/6N * SJL	N	25320092
MGI:5707924	M	MP:0005578	teratozoospermia	Ube2j1<tm1.2Hpl>/Ube2j1<tm1.2Hpl>	involves: BALB/cJ * C57BL/6 * C57BL/6N * SJL	N	25320092
MGI:5707924	M	MP:0006380	abnormal spermatid morphology	Ube2j1<tm1.2Hpl>/Ube2j1<tm1.2Hpl>	involves: BALB/cJ * C57BL/6 * C57BL/6N * SJL	N	25320092
MGI:5707924	M	MP:0002673	abnormal sperm number	Ube2j1<tm1.2Hpl>/Ube2j1<tm1.2Hpl>	involves: BALB/cJ * C57BL/6 * C57BL/6N * SJL	N	25320092
MGI:5707924	M	MP:0008898	abnormal acrosome morphology	Ube2j1<tm1.2Hpl>/Ube2j1<tm1.2Hpl>	involves: BALB/cJ * C57BL/6 * C57BL/6N * SJL	N	25320092
MGI:5707924	M	MP:0002675	asthenozoospermia	Ube2j1<tm1.2Hpl>/Ube2j1<tm1.2Hpl>	involves: BALB/cJ * C57BL/6 * C57BL/6N * SJL	N	25320092
MGI:5707924	M	MP:0001925	male infertility	Ube2j1<tm1.2Hpl>/Ube2j1<tm1.2Hpl>	involves: BALB/cJ * C57BL/6 * C57BL/6N * SJL	N	25320092
MGI:5707924	M	MP:0005410	abnormal fertilization	Ube2j1<tm1.2Hpl>/Ube2j1<tm1.2Hpl>	involves: BALB/cJ * C57BL/6 * C57BL/6N * SJL	N	25320092
MGI:5707947	F	MP:0013784	abnormal mammary gland bud elongation	Net1<tm1.2Jafr>/Net1<tm1.2Jafr>	involves: C57BL/6 * SJL	N	25321414
MGI:5707947	F	MP:0000662	abnormal branching of the mammary ductal tree	Net1<tm1.2Jafr>/Net1<tm1.2Jafr>	involves: C57BL/6 * SJL	N	25321414
MGI:5707947	F	MP:0000628	abnormal mammary gland development	Net1<tm1.2Jafr>/Net1<tm1.2Jafr>	involves: C57BL/6 * SJL	N	25321414
MGI:5707947	F	MP:0008904	abnormal mammary fat pad morphology	Net1<tm1.2Jafr>/Net1<tm1.2Jafr>	involves: C57BL/6 * SJL	N	25321414
MGI:5708101	F	MP:0012688	abnormal heart ventricles weight	Ankrd1<tm1.2Jmda>/Ankrd1<+>	involves: 129S6/SvEvTac * C57BL/6J	N	25452119
MGI:5708372	M	MP:0008489	slow postnatal weight gain	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0006362	abnormal male germ cell morphology	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0001262	decreased body weight	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0008975	delayed male fertility	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0013601	increased testis apoptosis	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0001752	abnormal hypothalamus secretion	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0002780	decreased circulating testosterone level	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0001938	delayed sexual maturation	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0000837	abnormal hypothalamus morphology	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0008940	delayed balanopreputial separation	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0001147	small testis	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0002216	abnormal seminiferous tubule morphology	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0002673	abnormal sperm number	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0005250	decreased Sertoli cell number	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708372	M	MP:0004852	decreased testis weight	Alk<tm1.1Rhp>/Alk<tm1.1Rhp>	involves: 129 * C57BL/6N	N	25955180
MGI:5708406	F	MP:0001405	impaired coordination	Sacs<tm2Bebr>/Sacs<+>	involves: C57BL/6	N	25260547
MGI:5708587	F	MP:0011617	abnormal habituation	Tg(Thy1-APPSweArc)BLngn/0	B6J.Cg-Tg(Thy1-APPSweArc)BLngn	N	20615433
MGI:5708587	F	MP:0003329	amyloid beta deposits	Tg(Thy1-APPSweArc)BLngn/0	B6J.Cg-Tg(Thy1-APPSweArc)BLngn	N	20615433
MGI:5708587	F	MP:0001458	abnormal object recognition memory	Tg(Thy1-APPSweArc)BLngn/0	B6J.Cg-Tg(Thy1-APPSweArc)BLngn	N	20615433
MGI:5708587	F	MP:0001262	decreased body weight	Tg(Thy1-APPSweArc)BLngn/0	B6J.Cg-Tg(Thy1-APPSweArc)BLngn	N	20615433
MGI:5708587	F	MP:0011942	decreased fluid intake	Tg(Thy1-APPSweArc)BLngn/0	B6J.Cg-Tg(Thy1-APPSweArc)BLngn	N	20615433
MGI:5708587	F	MP:0012317	impaired conditioning behavior	Tg(Thy1-APPSweArc)BLngn/0	B6J.Cg-Tg(Thy1-APPSweArc)BLngn	N	20615433
MGI:5708587	F	MP:0001417	decreased exploration in new environment	Tg(Thy1-APPSweArc)BLngn/0	B6J.Cg-Tg(Thy1-APPSweArc)BLngn	N	20615433
MGI:5708587	F	MP:0004000	impaired passive avoidance behavior	Tg(Thy1-APPSweArc)BLngn/0	B6J.Cg-Tg(Thy1-APPSweArc)BLngn	N	20615433
MGI:5708587	F	MP:0001408	stereotypic behavior	Tg(Thy1-APPSweArc)BLngn/0	B6J.Cg-Tg(Thy1-APPSweArc)BLngn	N	20615433
MGI:5708587	F	MP:0010698	abnormal impulsive behavior control	Tg(Thy1-APPSweArc)BLngn/0	B6J.Cg-Tg(Thy1-APPSweArc)BLngn	N	20615433
MGI:5749220	F	MP:0001926	female infertility	Marf1<m1Rpg>/Marf1<m1Rpg>	B6;C3Fe-Marf1<m1Rpg>/J	N	22442484
MGI:5749220	F	MP:0010767	abnormal female meiosis I arrest	Marf1<m1Rpg>/Marf1<m1Rpg>	B6;C3Fe-Marf1<m1Rpg>/J	N	22442484
MGI:5749248	F	MP:0005498	hyporesponsive to tactile stimuli	Sod1<m1H>/Sod1<m1H>	involves: C3H/HeH * C57BL/6J	N	25468678
MGI:5749248	F	MP:0001973	increased thermal nociceptive threshold	Sod1<m1H>/Sod1<m1H>	involves: C3H/HeH * C57BL/6J	N	25468678
MGI:5749248	F	MP:0000748	progressive muscle weakness	Sod1<m1H>/Sod1<m1H>	involves: C3H/HeH * C57BL/6J	N	25468678
MGI:5749563	M	MP:0001405	impaired coordination	Mecp2<tm1Bird>/Y,Pvalb<tm1.1(cre)Aibs>/Pvalb<+>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl	N	26590342
MGI:5749563	M	MP:0001393	ataxia	Mecp2<tm1Bird>/Y,Pvalb<tm1.1(cre)Aibs>/Pvalb<+>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl	N	26590342
MGI:5749563	M	MP:0009456	impaired cued conditioning behavior	Mecp2<tm1Bird>/Y,Pvalb<tm1.1(cre)Aibs>/Pvalb<+>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl	N	26590342
MGI:5749563	M	MP:0002083	premature death	Mecp2<tm1Bird>/Y,Pvalb<tm1.1(cre)Aibs>/Pvalb<+>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl	N	26590342
MGI:5749563	M	MP:0001360	abnormal social investigation	Mecp2<tm1Bird>/Y,Pvalb<tm1.1(cre)Aibs>/Pvalb<+>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl	N	26590342
MGI:5749563	M	MP:0001406	abnormal gait	Mecp2<tm1Bird>/Y,Pvalb<tm1.1(cre)Aibs>/Pvalb<+>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl	N	26590342
MGI:5749563	M	MP:0001489	decreased startle reflex	Mecp2<tm1Bird>/Y,Pvalb<tm1.1(cre)Aibs>/Pvalb<+>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl	N	26590342
MGI:5749568	M	MP:0002083	premature death	Mecp2<tm1Bird>/Y,Sst<tm2.1(cre)Zjh>/Sst<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	26590342
MGI:5749568	M	MP:0003997	tonic-clonic seizures	Mecp2<tm1Bird>/Y,Sst<tm2.1(cre)Zjh>/Sst<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	26590342
MGI:5749568	M	MP:0002064	seizures	Mecp2<tm1Bird>/Y,Sst<tm2.1(cre)Zjh>/Sst<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	26590342
MGI:5749568	M	MP:0001409	increased stereotypic behavior	Mecp2<tm1Bird>/Y,Sst<tm2.1(cre)Zjh>/Sst<+>	involves: 129P2/OlaHsd * 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	26590342
MGI:5749679	M	MP:0002169	no abnormal phenotype detected	Gpr17<tm1(KOMP)Vlcg>/Gpr17<tm1(KOMP)Vlcg>	C57BL/6NTac-Gpr17<tm1(KOMP)Vlcg>	N	25624481
MGI:5749790	F	MP:0012307	impaired spatial learning	Tg(Camk2a-MAPT)601Ymot/0	involves: C57BL/6 * C57BL/6J	N	21324362
MGI:5749790	F	MP:0004080	abnormal nucleus accumbens morphology	Tg(Camk2a-MAPT)601Ymot/0	involves: C57BL/6 * C57BL/6J	N	21324362
MGI:5749790	F	MP:0005404	abnormal axon morphology	Tg(Camk2a-MAPT)601Ymot/0	involves: C57BL/6 * C57BL/6J	N	21324362
MGI:5749790	F	MP:0009936	abnormal dendritic spine morphology	Tg(Camk2a-MAPT)601Ymot/0	involves: C57BL/6 * C57BL/6J	N	21324362
MGI:5749790	F	MP:0009538	abnormal synapse morphology	Tg(Camk2a-MAPT)601Ymot/0	involves: C57BL/6 * C57BL/6J	N	21324362
MGI:5749790	F	MP:0008428	abnormal spatial working memory	Tg(Camk2a-MAPT)601Ymot/0	involves: C57BL/6 * C57BL/6J	N	21324362
MGI:5749790	F	MP:0001364	decreased anxiety-related response	Tg(Camk2a-MAPT)601Ymot/0	involves: C57BL/6 * C57BL/6J	N	21324362
MGI:5749790	F	MP:0002063	abnormal learning/memory/conditioning	Tg(Camk2a-MAPT)601Ymot/0	involves: C57BL/6 * C57BL/6J	N	21324362
MGI:5749790	F	MP:0003926	decreased cellular glucose uptake	Tg(Camk2a-MAPT)601Ymot/0	involves: C57BL/6 * C57BL/6J	N	21324362
MGI:5749806	M	MP:0009356	decreased liver triglyceride level	Tg(Adipoq-LPL)1Fnln/?	B6.Cg-Tg(Adipoq-LPL)1Fnln	N	25784555
MGI:5749806	M	MP:0000186	decreased circulating HDL cholesterol level	Tg(Adipoq-LPL)1Fnln/?	B6.Cg-Tg(Adipoq-LPL)1Fnln	N	25784555
MGI:5749806	M	MP:0005659	decreased susceptibility to diet-induced obesity	Tg(Adipoq-LPL)1Fnln/?	B6.Cg-Tg(Adipoq-LPL)1Fnln	N	25784555
MGI:5749806	M	MP:0030969	increased circulating adiponectin level	Tg(Adipoq-LPL)1Fnln/?	B6.Cg-Tg(Adipoq-LPL)1Fnln	N	25784555
MGI:5749806	M	MP:0009355	increased liver triglyceride level	Tg(Adipoq-LPL)1Fnln/?	B6.Cg-Tg(Adipoq-LPL)1Fnln	N	25784555
MGI:5749806	M	MP:0000183	decreased circulating LDL cholesterol level	Tg(Adipoq-LPL)1Fnln/?	B6.Cg-Tg(Adipoq-LPL)1Fnln	N	25784555
MGI:5749806	M	MP:0002891	increased insulin sensitivity	Tg(Adipoq-LPL)1Fnln/?	B6.Cg-Tg(Adipoq-LPL)1Fnln	N	25784555
MGI:5749806	M	MP:0005292	improved glucose tolerance	Tg(Adipoq-LPL)1Fnln/?	B6.Cg-Tg(Adipoq-LPL)1Fnln	N	25784555
MGI:5749806	M	MP:0005179	decreased circulating cholesterol level	Tg(Adipoq-LPL)1Fnln/?	B6.Cg-Tg(Adipoq-LPL)1Fnln	N	25784555
MGI:5749806	M	MP:0013278	decreased fasting circulating glucose level	Tg(Adipoq-LPL)1Fnln/?	B6.Cg-Tg(Adipoq-LPL)1Fnln	N	25784555
MGI:5749824	M	MP:0008893	detached sperm flagellum	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0009833	absent sperm mitochondrial sheath	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0009831	abnormal sperm midpiece morphology	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0009834	abnormal sperm annulus morphology	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0002675	asthenozoospermia	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0009234	absent sperm head	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0009837	abnormal sperm end piece morphology	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0009830	abnormal sperm connecting piece morphology	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0002687	oligozoospermia	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0002662	abnormal cauda epididymis morphology	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0008892	abnormal sperm flagellum morphology	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0001925	male infertility	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0005578	teratozoospermia	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0006380	abnormal spermatid morphology	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5749824	M	MP:0001932	abnormal spermiogenesis	Spata6<tm1a(KOMP)Wtsi>/Spata6<tm1a(KOMP)Wtsi>	B6J.B6N-Spata6<tm1a(KOMP)Wtsi>	N	25605924
MGI:5750127	F	MP:0008044	increased NK cell number	Tspo<tm1.1Guwu>/Tspo<tm1.1Guwu>	involves: C57BL/6	N	25406832
MGI:5750966	M	MP:0002687	oligozoospermia	Shcbp1l<tm1a(KOMP)Wtsi>/Shcbp1l<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	24557841
MGI:5750966	M	MP:0001935	decreased litter size	Shcbp1l<tm1a(KOMP)Wtsi>/Shcbp1l<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	24557841
MGI:5750966	M	MP:0014052	increased male germ cell apoptosis	Shcbp1l<tm1a(KOMP)Wtsi>/Shcbp1l<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	24557841
MGI:5750966	M	MP:0009761	abnormal meiotic spindle morphology	Shcbp1l<tm1a(KOMP)Wtsi>/Shcbp1l<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	24557841
MGI:5750966	M	MP:0001922	reduced male fertility	Shcbp1l<tm1a(KOMP)Wtsi>/Shcbp1l<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	24557841
MGI:5750966	M	MP:0008261	arrest of male meiosis	Shcbp1l<tm1a(KOMP)Wtsi>/Shcbp1l<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	24557841
MGI:5750966	M	MP:0004852	decreased testis weight	Shcbp1l<tm1a(KOMP)Wtsi>/Shcbp1l<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	24557841
MGI:5750971	F	MP:0012073	premature mammary gland growth during pregnancy	Mir193b<tm1.2Mam>/Mir193b<tm1.2Mam>	involves: 129S6/SvEvTac * C57BL/6NTac	N	25236432
MGI:5750971	F	MP:0010172	abnormal mammary gland epithelium physiology	Mir193b<tm1.2Mam>/Mir193b<tm1.2Mam>	involves: 129S6/SvEvTac * C57BL/6NTac	N	25236432
MGI:5750971	F	MP:0009504	abnormal mammary gland epithelium morphology	Mir193b<tm1.2Mam>/Mir193b<tm1.2Mam>	involves: 129S6/SvEvTac * C57BL/6NTac	N	25236432
MGI:5751088	F	MP:0002637	small uterus	Ash1l<Gt(AL0395)Wtsi>/Ash1l<Gt(AL0395)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	26333994
MGI:5751088	M	MP:0002631	abnormal epididymis morphology	Ash1l<Gt(AL0395)Wtsi>/Ash1l<Gt(AL0395)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	26333994
MGI:5751088	F	MP:0001926	female infertility	Ash1l<Gt(AL0395)Wtsi>/Ash1l<Gt(AL0395)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	26333994
MGI:5751088	M	MP:0002662	abnormal cauda epididymis morphology	Ash1l<Gt(AL0395)Wtsi>/Ash1l<Gt(AL0395)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	26333994
MGI:5751088	F	MP:0009669	abnormal postimplantation uterine environment	Ash1l<Gt(AL0395)Wtsi>/Ash1l<Gt(AL0395)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	26333994
MGI:5751088	F	MP:0009096	decreased endometrial gland number	Ash1l<Gt(AL0395)Wtsi>/Ash1l<Gt(AL0395)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	26333994
MGI:5751088	M	MP:0008853	decreased abdominal adipose tissue amount	Ash1l<Gt(AL0395)Wtsi>/Ash1l<Gt(AL0395)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	26333994
MGI:5751088	M	MP:0001922	reduced male fertility	Ash1l<Gt(AL0395)Wtsi>/Ash1l<Gt(AL0395)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	26333994
MGI:5751088	F	MP:0008258	thin endometrium	Ash1l<Gt(AL0395)Wtsi>/Ash1l<Gt(AL0395)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	26333994
MGI:5751088	F	MP:0001120	abnormal uterus morphology	Ash1l<Gt(AL0395)Wtsi>/Ash1l<Gt(AL0395)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	26333994
MGI:5751088	M	MP:0002769	abnormal vas deferens morphology	Ash1l<Gt(AL0395)Wtsi>/Ash1l<Gt(AL0395)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	26333994
MGI:5751088	F	MP:0003845	abnormal decidualization	Ash1l<Gt(AL0395)Wtsi>/Ash1l<Gt(AL0395)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	26333994
MGI:5751088	M	MP:0002673	abnormal sperm number	Ash1l<Gt(AL0395)Wtsi>/Ash1l<Gt(AL0395)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	26333994
MGI:5751123	M	MP:0004000	impaired passive avoidance behavior	Htr2c<tm1Arte>/Y	involves: C57BL/6	N	25257581
MGI:5751123	M	MP:0003063	increased coping response	Htr2c<tm1Arte>/Y	involves: C57BL/6	N	25257581
MGI:5751123	M	MP:0005376	homeostasis/metabolism phenotype	Htr2c<tm1Arte>/Y	involves: C57BL/6	Y	25257581
MGI:5751123	M	MP:0005386	behavior/neurological phenotype	Htr2c<tm1Arte>/Y	involves: C57BL/6	Y	25257581
MGI:5751123	M	MP:0001745	increased circulating corticosterone level	Htr2c<tm1Arte>/Y	involves: C57BL/6	N	25257581
MGI:5751481	M	MP:0003205	testicular atrophy	Celsr1<ctb-2J>/Celsr1<ctb-2J>	STOCK Celsr1<ctb-2J>/GrsrJ	N	MGI:5751443
MGI:5751516	M	MP:0001922	reduced male fertility	Iqcf1<em1Zdq>/Iqcf1<em1Zdq>	Not Specified	N	25380116
MGI:5751516	M	MP:0005389	reproductive system phenotype	Iqcf1<em1Zdq>/Iqcf1<em1Zdq>	Not Specified	Y	25380116
MGI:5751516	M	MP:0002675	asthenozoospermia	Iqcf1<em1Zdq>/Iqcf1<em1Zdq>	Not Specified	N	25380116
MGI:5751516	M	MP:0004542	impaired acrosome reaction	Iqcf1<em1Zdq>/Iqcf1<em1Zdq>	Not Specified	N	25380116
MGI:5751522	M	MP:0003205	testicular atrophy	Celsr1<ctb>/Celsr1<ctb>	CByJ.Cg-Celsr1<ctb>/GrsrJ	N	MGI:5751443
MGI:5751539	F	MP:0013278	decreased fasting circulating glucose level	Sox17<SHIVA>/Sox17<+>	either: C57BL/6-Sox17<SHIVA> or (involves: C57BL/6 * C3H/HeN)	N	25141153
MGI:5751539	F	MP:0009703	decreased birth body size	Sox17<SHIVA>/Sox17<+>	either: C57BL/6-Sox17<SHIVA> or (involves: C57BL/6 * C3H/HeN)	N	25141153
MGI:5751539	F	MP:0004833	ovary atrophy	Sox17<SHIVA>/Sox17<+>	either: C57BL/6-Sox17<SHIVA> or (involves: C57BL/6 * C3H/HeN)	N	25141153
MGI:5751539	F	MP:0000186	decreased circulating HDL cholesterol level	Sox17<SHIVA>/Sox17<+>	either: C57BL/6-Sox17<SHIVA> or (involves: C57BL/6 * C3H/HeN)	N	25141153
MGI:5751539	F	MP:0014010	abnormal peroxisome morphology	Sox17<SHIVA>/Sox17<+>	either: C57BL/6-Sox17<SHIVA> or (involves: C57BL/6 * C3H/HeN)	N	25141153
MGI:5751539	F	MP:0005266	abnormal metabolism	Sox17<SHIVA>/Sox17<+>	either: C57BL/6-Sox17<SHIVA> or (involves: C57BL/6 * C3H/HeN)	N	25141153
MGI:5751539	F	MP:0013245	abnormal lipid metabolism	Sox17<SHIVA>/Sox17<+>	either: C57BL/6-Sox17<SHIVA> or (involves: C57BL/6 * C3H/HeN)	N	25141153
MGI:5751539	F	MP:0001923	reduced female fertility	Sox17<SHIVA>/Sox17<+>	either: C57BL/6-Sox17<SHIVA> or (involves: C57BL/6 * C3H/HeN)	N	25141153
MGI:5751539	F	MP:0009356	decreased liver triglyceride level	Sox17<SHIVA>/Sox17<+>	either: C57BL/6-Sox17<SHIVA> or (involves: C57BL/6 * C3H/HeN)	N	25141153
MGI:5751539	F	MP:0003458	decreased circulating ketone body level	Sox17<SHIVA>/Sox17<+>	either: C57BL/6-Sox17<SHIVA> or (involves: C57BL/6 * C3H/HeN)	N	25141153
MGI:5751539	F	MP:0005319	abnormal enzyme/coenzyme level	Sox17<SHIVA>/Sox17<+>	either: C57BL/6-Sox17<SHIVA> or (involves: C57BL/6 * C3H/HeN)	N	25141153
MGI:5751550	M	MP:0001552	increased circulating triglyceride level	Tg(Vil1-cre)997Gum/?,Tlr5<tm1.1Gewr>/Tlr5<tm1.1Gewr>	involves: C57BL/6J * C57BL/6NTac * SJL/J	N	25172014
MGI:5751550	M	MP:0005178	increased circulating cholesterol level	Tg(Vil1-cre)997Gum/?,Tlr5<tm1.1Gewr>/Tlr5<tm1.1Gewr>	involves: C57BL/6J * C57BL/6NTac * SJL/J	N	25172014
MGI:5751707	M	MP:0003233	prolonged QT interval	Mecp2<tm1.1Irsf>/Y	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751707	M	MP:0002912	abnormal excitatory postsynaptic potential	Mecp2<tm1.1Irsf>/Y	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751707	M	MP:0001473	reduced long-term potentiation	Mecp2<tm1.1Irsf>/Y	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751707	M	MP:0009454	impaired contextual conditioning behavior	Mecp2<tm1.1Irsf>/Y	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751707	M	MP:0001364	decreased anxiety-related response	Mecp2<tm1.1Irsf>/Y	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751707	M	MP:0001636	irregular heartbeat	Mecp2<tm1.1Irsf>/Y	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751707	M	MP:0002175	decreased brain weight	Mecp2<tm1.1Irsf>/Y	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751707	M	MP:0001405	impaired coordination	Mecp2<tm1.1Irsf>/Y	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751707	M	MP:0001262	decreased body weight	Mecp2<tm1.1Irsf>/Y	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751707	M	MP:0005573	increased pulmonary respiratory rate	Mecp2<tm1.1Irsf>/Y	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751707	M	MP:0002083	premature death	Mecp2<tm1.1Irsf>/Y	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751716	F	MP:0002083	premature death	Mecp2<tm1.1Irsf>/Mecp2<+>	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751716	F	MP:0003997	tonic-clonic seizures	Mecp2<tm1.1Irsf>/Mecp2<+>	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751716	F	MP:0002833	increased heart weight	Mecp2<tm1.1Irsf>/Mecp2<+>	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751716	F	MP:0003233	prolonged QT interval	Mecp2<tm1.1Irsf>/Mecp2<+>	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751716	F	MP:0005573	increased pulmonary respiratory rate	Mecp2<tm1.1Irsf>/Mecp2<+>	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751716	F	MP:0001405	impaired coordination	Mecp2<tm1.1Irsf>/Mecp2<+>	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751716	F	MP:0002981	increased liver weight	Mecp2<tm1.1Irsf>/Mecp2<+>	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751716	F	MP:0001260	increased body weight	Mecp2<tm1.1Irsf>/Mecp2<+>	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5751716	F	MP:0002175	decreased brain weight	Mecp2<tm1.1Irsf>/Mecp2<+>	involves: 129S2/SvPas * C57BL/6	N	25634563
MGI:5752189	F	MP:0010299	increased mammary gland tumor incidence	Pten<tm2Mak>/Pten<tm2Mak>,Tg(MMTV-cre)#Tfln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	25330770
MGI:5752189	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Pten<tm2Mak>/Pten<tm2Mak>,Tg(MMTV-cre)#Tfln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	25330770
MGI:5752189	F	MP:0012043	increased myoepithelioma incidence	Pten<tm2Mak>/Pten<tm2Mak>,Tg(MMTV-cre)#Tfln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	25330770
MGI:5752189	F	MP:0010367	increased spindle cell carcinoma incidence	Pten<tm2Mak>/Pten<tm2Mak>,Tg(MMTV-cre)#Tfln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	25330770
MGI:5752189	F	MP:0001883	increased mammary adenocarcinoma incidence	Pten<tm2Mak>/Pten<tm2Mak>,Tg(MMTV-cre)#Tfln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	25330770
MGI:5752190	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Pten<tm2Mak>/Pten<tm2Mak>,Tg(Wap-cre)11738Mam/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	25330770
MGI:5752190	F	MP:0010299	increased mammary gland tumor incidence	Pten<tm2Mak>/Pten<tm2Mak>,Tg(Wap-cre)11738Mam/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	25330770
MGI:5752190	F	MP:0001883	increased mammary adenocarcinoma incidence	Pten<tm2Mak>/Pten<tm2Mak>,Tg(Wap-cre)11738Mam/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	25330770
MGI:5752190	F	MP:0010367	increased spindle cell carcinoma incidence	Pten<tm2Mak>/Pten<tm2Mak>,Tg(Wap-cre)11738Mam/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	25330770
MGI:5752190	F	MP:0012043	increased myoepithelioma incidence	Pten<tm2Mak>/Pten<tm2Mak>,Tg(Wap-cre)11738Mam/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	25330770
MGI:5752193	F	MP:0010367	increased spindle cell carcinoma incidence	Pten<tm2Mak>/Pten<tm2Mak>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(MMTV-cre)#Tfln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	25330770
MGI:5752193	F	MP:0010299	increased mammary gland tumor incidence	Pten<tm2Mak>/Pten<tm2Mak>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(MMTV-cre)#Tfln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	25330770
MGI:5752193	F	MP:0001883	increased mammary adenocarcinoma incidence	Pten<tm2Mak>/Pten<tm2Mak>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(MMTV-cre)#Tfln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	25330770
MGI:5752193	F	MP:0012043	increased myoepithelioma incidence	Pten<tm2Mak>/Pten<tm2Mak>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(MMTV-cre)#Tfln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	25330770
MGI:5752196	F	MP:0001883	increased mammary adenocarcinoma incidence	Pten<tm2Mak>/Pten<tm2Mak>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)11738Mam/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	25330770
MGI:5752196	F	MP:0010299	increased mammary gland tumor incidence	Pten<tm2Mak>/Pten<tm2Mak>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)11738Mam/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	25330770
MGI:5752196	F	MP:0012043	increased myoepithelioma incidence	Pten<tm2Mak>/Pten<tm2Mak>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)11738Mam/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	25330770
MGI:5752196	F	MP:0010367	increased spindle cell carcinoma incidence	Pten<tm2Mak>/Pten<tm2Mak>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)11738Mam/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	25330770
MGI:5752199	F	MP:0012043	increased myoepithelioma incidence	Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(MMTV-cre)#Tfln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	25330770
MGI:5752199	F	MP:0001883	increased mammary adenocarcinoma incidence	Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(MMTV-cre)#Tfln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	25330770
MGI:5752199	F	MP:0010367	increased spindle cell carcinoma incidence	Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(MMTV-cre)#Tfln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	25330770
MGI:5752199	F	MP:0010299	increased mammary gland tumor incidence	Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(MMTV-cre)#Tfln/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	N	25330770
MGI:5752786	F	MP:0031391	increased locomotor activity	Disc1<m1H>/Disc1<m1H>	B6N.C(C3H)-Disc1<m1H>	N	26728762
MGI:5752786	F	MP:0002797	increased thigmotaxis	Disc1<m1H>/Disc1<m1H>	B6N.C(C3H)-Disc1<m1H>	N	26728762
MGI:5752786	M	MP:0002757	decreased vertical activity	Disc1<m1H>/Disc1<m1H>	B6N.C(C3H)-Disc1<m1H>	N	26728762
MGI:5752786	F	MP:0001417	decreased exploration in new environment	Disc1<m1H>/Disc1<m1H>	B6N.C(C3H)-Disc1<m1H>	N	26728762
MGI:5752786	F	MP:0001360	abnormal social investigation	Disc1<m1H>/Disc1<m1H>	B6N.C(C3H)-Disc1<m1H>	N	26728762
MGI:5752786	F	MP:0004000	impaired passive avoidance behavior	Disc1<m1H>/Disc1<m1H>	B6N.C(C3H)-Disc1<m1H>	N	26728762
MGI:5752786	F	MP:0001363	increased anxiety-related response	Disc1<m1H>/Disc1<m1H>	B6N.C(C3H)-Disc1<m1H>	N	26728762
MGI:5752793	M	MP:0002834	decreased heart weight	Rhobtb3<tm1a(KOMP)Wtsi>/Rhobtb3<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	24923387
MGI:5752793	M	MP:0004953	decreased spleen weight	Rhobtb3<tm1a(KOMP)Wtsi>/Rhobtb3<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	24923387
MGI:5752793	M	MP:0004852	decreased testis weight	Rhobtb3<tm1a(KOMP)Wtsi>/Rhobtb3<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	24923387
MGI:5753052	M	MP:0005178	increased circulating cholesterol level	Dnajc7<tm1.2Neg>/Dnajc7<tm1.2Neg>	involves: 129S/SvEv * C57BL/6 * CBA	N	25542016
MGI:5753052	M	MP:0002628	hepatic steatosis	Dnajc7<tm1.2Neg>/Dnajc7<tm1.2Neg>	involves: 129S/SvEv * C57BL/6 * CBA	N	25542016
MGI:5754492	F	MP:0001260	increased body weight	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	N	25574869
MGI:5754492	F	MP:0001927	abnormal estrous cycle	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	N	25574869
MGI:5754492	M	MP:0002790	decreased circulating follicle stimulating hormone level	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	N	25574869
MGI:5754492	F	MP:0001938	delayed sexual maturation	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	N	25574869
MGI:5754492	F	MP:0009020	prolonged metestrus	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	N	25574869
MGI:5754492	F	MP:0001935	decreased litter size	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	N	25574869
MGI:5754492	F	MP:0009011	prolonged diestrus	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	N	25574869
MGI:5754492	F	MP:0001134	absent corpus luteum	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	N	25574869
MGI:5754492	F	MP:0001923	reduced female fertility	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	N	25574869
MGI:5754492	M	MP:0005389	reproductive system phenotype	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	Y	25574869
MGI:5754492	F	MP:0002636	delayed vaginal opening	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	N	25574869
MGI:5754492	F	MP:0004856	decreased ovary weight	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	N	25574869
MGI:5754492	F	MP:0003377	late onset of menarche	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	N	25574869
MGI:5754492	M	MP:0003550	short perineum	Tac2<tm1Tigm>/Tac2<tm1Tigm>	involves: 129 * C57BL/6	N	25574869
MGI:5754810	M	MP:0005179	decreased circulating cholesterol level	Gpat3<tm1Reg>/Gpat3<tm1Reg>	involves: C57BL/6	N	24714397
MGI:5754810	F	MP:0010025	decreased total body fat amount	Gpat3<tm1Reg>/Gpat3<tm1Reg>	involves: C57BL/6	N	24714397
MGI:5754810	M	MP:0002941	increased circulating alanine transaminase level	Gpat3<tm1Reg>/Gpat3<tm1Reg>	involves: C57BL/6	N	24714397
MGI:5754810	F	MP:0005659	decreased susceptibility to diet-induced obesity	Gpat3<tm1Reg>/Gpat3<tm1Reg>	involves: C57BL/6	N	24714397
MGI:5754810	M	MP:0005343	increased circulating aspartate transaminase level	Gpat3<tm1Reg>/Gpat3<tm1Reg>	involves: C57BL/6	N	24714397
MGI:5754810	M	MP:0010027	increased liver cholesterol level	Gpat3<tm1Reg>/Gpat3<tm1Reg>	involves: C57BL/6	N	24714397
MGI:5754810	M	MP:0005376	homeostasis/metabolism phenotype	Gpat3<tm1Reg>/Gpat3<tm1Reg>	involves: C57BL/6	Y	24714397
MGI:5754810	M	MP:0005292	improved glucose tolerance	Gpat3<tm1Reg>/Gpat3<tm1Reg>	involves: C57BL/6	N	24714397
MGI:5754810	F	MP:0008907	decreased total fat pad weight	Gpat3<tm1Reg>/Gpat3<tm1Reg>	involves: C57BL/6	N	24714397
MGI:5754810	M	MP:0001780	decreased brown adipose tissue amount	Gpat3<tm1Reg>/Gpat3<tm1Reg>	involves: C57BL/6	N	24714397
MGI:5755043	F	MP:0001364	decreased anxiety-related response	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	N	25697701
MGI:5755043	F	MP:0001262	decreased body weight	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	N	25697701
MGI:5755043	F	MP:0001513	limb grasping	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	N	25697701
MGI:5755045	F	MP:0001935	decreased litter size	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax	N	25697701
MGI:5755045	M	MP:0010047	axonal spheroids	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax	N	25697701
MGI:5755045	F	MP:0001385	pup cannibalization	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax	N	25697701
MGI:5755045	M	MP:0000754	paresis	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax	N	25697701
MGI:5755045	M	MP:0005150	cachexia	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax	N	25697701
MGI:5755045	F	MP:0012307	impaired spatial learning	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax	N	25697701
MGI:5755045	F	MP:0001522	impaired swimming	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax	N	25697701
MGI:5755045	M	MP:0001504	abnormal posture	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax	N	25697701
MGI:5755045	F	MP:0001364	decreased anxiety-related response	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax	N	25697701
MGI:5755045	F	MP:0001262	decreased body weight	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax	N	25697701
MGI:5755045	F	MP:0001513	limb grasping	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax	N	25697701
MGI:5755045	F	MP:0008414	abnormal spatial reference memory	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax	N	25697701
MGI:5755137	M	MP:0002807	abnormal eye blink conditioning behavior	Dp(7Herc2-Mkrn3)1Taku/0	B6J.129S7-Dp(7Herc2-Mkrn3)1Taku	N	25418414
MGI:5755288	M	MP:0001265	decreased body size	Tg(SRY-YFP,Tyr)TashTNpln/Tg(SRY-YFP,Tyr)TashTNpln	involves: FVB/N	N	25786024
MGI:5755288	M	MP:0003270	intestinal obstruction	Tg(SRY-YFP,Tyr)TashTNpln/Tg(SRY-YFP,Tyr)TashTNpln	involves: FVB/N	N	25786024
MGI:5755288	M	MP:0002926	aganglionic megacolon	Tg(SRY-YFP,Tyr)TashTNpln/Tg(SRY-YFP,Tyr)TashTNpln	involves: FVB/N	N	25786024
MGI:5755836	M	MP:0005387	immune system phenotype	Ryr2<tm1.1Hnis>/Ryr2<tm1.1Hnis>	involves: C57BL/6	Y	25087098
MGI:5755836	M	MP:0005367	renal/urinary system phenotype	Ryr2<tm1.1Hnis>/Ryr2<tm1.1Hnis>	involves: C57BL/6	Y	25087098
MGI:5755836	M	MP:0005232	abnormal mesenteric lymph node morphology	Ryr2<tm1.1Hnis>/Ryr2<tm1.1Hnis>	involves: C57BL/6	N	25087098
MGI:5755836	M	MP:0005378	growth/size/body region phenotype	Ryr2<tm1.1Hnis>/Ryr2<tm1.1Hnis>	involves: C57BL/6	Y	25087098
MGI:5755836	M	MP:0005385	cardiovascular system phenotype	Ryr2<tm1.1Hnis>/Ryr2<tm1.1Hnis>	involves: C57BL/6	Y	25087098
MGI:5755836	M	MP:0008466	enlarged mesenteric lymph nodes	Ryr2<tm1.1Hnis>/Ryr2<tm1.1Hnis>	involves: C57BL/6	N	25087098
MGI:5755836	M	MP:0002220	large lymphoid organs	Ryr2<tm1.1Hnis>/Ryr2<tm1.1Hnis>	involves: C57BL/6	N	25087098
MGI:5755836	M	MP:0003631	nervous system phenotype	Ryr2<tm1.1Hnis>/Ryr2<tm1.1Hnis>	involves: C57BL/6	Y	25087098
MGI:5755836	M	MP:0002357	abnormal spleen white pulp morphology	Ryr2<tm1.1Hnis>/Ryr2<tm1.1Hnis>	involves: C57BL/6	N	25087098
MGI:5755836	M	MP:0004955	increased thymus weight	Ryr2<tm1.1Hnis>/Ryr2<tm1.1Hnis>	involves: C57BL/6	N	25087098
MGI:5755836	M	MP:0004952	increased spleen weight	Ryr2<tm1.1Hnis>/Ryr2<tm1.1Hnis>	involves: C57BL/6	N	25087098
MGI:5755836	M	MP:0009559	thymus cortex hyperplasia	Ryr2<tm1.1Hnis>/Ryr2<tm1.1Hnis>	involves: C57BL/6	N	25087098
MGI:5755852	F	MP:0013778	abnormal mammary gland myoepithelium morphology	Pik3ca<tm1.1Waph>/Pik3ca<+>,Tg(MMTV-cre)#Mam/0	involves: 129S1/Sv * C57BL/6 * FVB	N	22666336
MGI:5755852	F	MP:0010364	increased fibroadenoma incidence	Pik3ca<tm1.1Waph>/Pik3ca<+>,Tg(MMTV-cre)#Mam/0	involves: 129S1/Sv * C57BL/6 * FVB	N	22666336
MGI:5755852	F	MP:0014057	abnormal mammary gland stroma morphology	Pik3ca<tm1.1Waph>/Pik3ca<+>,Tg(MMTV-cre)#Mam/0	involves: 129S1/Sv * C57BL/6 * FVB	N	22666336
MGI:5755852	F	MP:0010299	increased mammary gland tumor incidence	Pik3ca<tm1.1Waph>/Pik3ca<+>,Tg(MMTV-cre)#Mam/0	involves: 129S1/Sv * C57BL/6 * FVB	N	22666336
MGI:5755852	F	MP:0009504	abnormal mammary gland epithelium morphology	Pik3ca<tm1.1Waph>/Pik3ca<+>,Tg(MMTV-cre)#Mam/0	involves: 129S1/Sv * C57BL/6 * FVB	N	22666336
MGI:5755852	F	MP:0009503	abnormal mammary gland duct morphology	Pik3ca<tm1.1Waph>/Pik3ca<+>,Tg(MMTV-cre)#Mam/0	involves: 129S1/Sv * C57BL/6 * FVB	N	22666336
MGI:5755852	F	MP:0013782	abnormal mammary duct terminal end bud morphology	Pik3ca<tm1.1Waph>/Pik3ca<+>,Tg(MMTV-cre)#Mam/0	involves: 129S1/Sv * C57BL/6 * FVB	N	22666336
MGI:5755852	F	MP:0003789	increased osteosarcoma incidence	Pik3ca<tm1.1Waph>/Pik3ca<+>,Tg(MMTV-cre)#Mam/0	involves: 129S1/Sv * C57BL/6 * FVB	N	22666336
MGI:5755852	F	MP:0010173	increased mammary gland epithelial cell proliferation	Pik3ca<tm1.1Waph>/Pik3ca<+>,Tg(MMTV-cre)#Mam/0	involves: 129S1/Sv * C57BL/6 * FVB	N	22666336
MGI:5755852	F	MP:0002083	premature death	Pik3ca<tm1.1Waph>/Pik3ca<+>,Tg(MMTV-cre)#Mam/0	involves: 129S1/Sv * C57BL/6 * FVB	N	22666336
MGI:5755852	F	MP:0000662	abnormal branching of the mammary ductal tree	Pik3ca<tm1.1Waph>/Pik3ca<+>,Tg(MMTV-cre)#Mam/0	involves: 129S1/Sv * C57BL/6 * FVB	N	22666336
MGI:5755852	F	MP:0006422	increased mammary adenoacanthoma incidence	Pik3ca<tm1.1Waph>/Pik3ca<+>,Tg(MMTV-cre)#Mam/0	involves: 129S1/Sv * C57BL/6 * FVB	N	22666336
MGI:5755852	F	MP:0002032	increased sarcoma incidence	Pik3ca<tm1.1Waph>/Pik3ca<+>,Tg(MMTV-cre)#Mam/0	involves: 129S1/Sv * C57BL/6 * FVB	N	22666336
MGI:5755966	M	MP:0000598	abnormal liver morphology	Tg(Alb-HBx)A112Tfts/0	involves: C57BL/6	N	16403455
MGI:5755966	M	MP:0003331	increased hepatocellular carcinoma incidence	Tg(Alb-HBx)A112Tfts/0	involves: C57BL/6	N	16403455
MGI:5755966	M	MP:0002941	increased circulating alanine transaminase level	Tg(Alb-HBx)A112Tfts/0	involves: C57BL/6	N	16403455
MGI:5755966	M	MP:0002628	hepatic steatosis	Tg(Alb-HBx)A112Tfts/0	involves: C57BL/6	N	16403455
MGI:5755966	M	MP:0005141	liver hyperplasia	Tg(Alb-HBx)A112Tfts/0	involves: C57BL/6	N	16403455
MGI:5755966	M	MP:0005517	impaired liver regeneration	Tg(Alb-HBx)A112Tfts/0	involves: C57BL/6	N	16403455
MGI:5756620	M	MP:0011100	preweaning lethality, complete penetrance	1700003F12Rik<tm1.1(KOMP)Vlcg>/1700003F12Rik<tm1.1(KOMP)Vlcg>	C57BL/6N-1700003F12Rik<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5756622	F	MP:0010052	increased grip strength	Pierce1<tm2b(EUCOMM)Wtsi>/Pierce1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Pierce1<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756623	F	MP:0002792	abnormal retina vasculature morphology	Prss3b<tm1b(KOMP)Wtsi>/Prss3b<tm1b(KOMP)Wtsi>	C57BL/6N-Prss3b<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756623	F	MP:0001399	hyperactivity	Prss3b<tm1b(KOMP)Wtsi>/Prss3b<tm1b(KOMP)Wtsi>	C57BL/6N-Prss3b<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756623	M	MP:0002942	decreased circulating alanine transaminase level	Prss3b<tm1b(KOMP)Wtsi>/Prss3b<tm1b(KOMP)Wtsi>	C57BL/6N-Prss3b<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756623	M	MP:0009142	decreased prepulse inhibition	Prss3b<tm1b(KOMP)Wtsi>/Prss3b<tm1b(KOMP)Wtsi>	C57BL/6N-Prss3b<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756624	M	MP:0001147	small testis	2510002D24Rik<tm1.1(KOMP)Vlcg>/2510002D24Rik<tm1.1(KOMP)Vlcg>	C57BL/6N-2510002D24Rik<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5756624	M	MP:0001146	abnormal testis morphology	2510002D24Rik<tm1.1(KOMP)Vlcg>/2510002D24Rik<tm1.1(KOMP)Vlcg>	C57BL/6N-2510002D24Rik<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5756624	M	MP:0004931	enlarged epididymis	2510002D24Rik<tm1.1(KOMP)Vlcg>/2510002D24Rik<tm1.1(KOMP)Vlcg>	C57BL/6N-2510002D24Rik<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5756624	M	MP:0002631	abnormal epididymis morphology	2510002D24Rik<tm1.1(KOMP)Vlcg>/2510002D24Rik<tm1.1(KOMP)Vlcg>	C57BL/6N-2510002D24Rik<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5756627	F	MP:0002764	short tibia	4933430I17Rik<tm1b(EUCOMM)Wtsi>/4933430I17Rik<tm1b(EUCOMM)Wtsi>	C57BL/6N-4933430I17Rik<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5756627	M	MP:0002941	increased circulating alanine transaminase level	4933430I17Rik<tm1b(EUCOMM)Wtsi>/4933430I17Rik<tm1b(EUCOMM)Wtsi>	C57BL/6N-4933430I17Rik<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5756627	F	MP:0005599	increased cardiac muscle contractility	4933430I17Rik<tm1b(EUCOMM)Wtsi>/4933430I17Rik<tm1b(EUCOMM)Wtsi>	C57BL/6N-4933430I17Rik<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5756628	M	MP:0002699	abnormal vitreous body morphology	Elapor1<tm1b(EUCOMM)Hmgu>/Elapor1<+>	C57BL/6N-Elapor1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756628	F	MP:0005559	increased circulating glucose level	Elapor1<tm1b(EUCOMM)Hmgu>/Elapor1<+>	C57BL/6N-Elapor1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756628	M	MP:0005016	decreased lymphocyte cell number	Elapor1<tm1b(EUCOMM)Hmgu>/Elapor1<+>	C57BL/6N-Elapor1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756628	M	MP:0001417	decreased exploration in new environment	Elapor1<tm1b(EUCOMM)Hmgu>/Elapor1<+>	C57BL/6N-Elapor1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756628	M	MP:0010097	abnormal retina blood vessel morphology	Elapor1<tm1b(EUCOMM)Hmgu>/Elapor1<+>	C57BL/6N-Elapor1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756628	M	MP:0011941	increased fluid intake	Elapor1<tm1b(EUCOMM)Hmgu>/Elapor1<+>	C57BL/6N-Elapor1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756628	M	MP:0002792	abnormal retina vasculature morphology	Elapor1<tm1b(EUCOMM)Hmgu>/Elapor1<+>	C57BL/6N-Elapor1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756630	F	MP:0003795	abnormal bone structure	Minar2<tm1b(KOMP)Wtsi>/Minar2<tm1b(KOMP)Wtsi>	C57BL/6N-Minar2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756630	M	MP:0001258	decreased body length	Minar2<tm1b(KOMP)Wtsi>/Minar2<tm1b(KOMP)Wtsi>	C57BL/6N-Minar2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756631	F	MP:0006243	impaired pupillary reflex	Aars2<tm1(KOMP)Wtsi>/Aars2<+>	C57BL/6N-Aars2<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5756631	F	MP:0003921	abnormal heart left ventricle morphology	Aars2<tm1(KOMP)Wtsi>/Aars2<+>	C57BL/6N-Aars2<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5756631	M	MP:0005011	increased eosinophil cell number	Aars2<tm1(KOMP)Wtsi>/Aars2<+>	C57BL/6N-Aars2<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5756631	M	MP:0002606	increased basophil cell number	Aars2<tm1(KOMP)Wtsi>/Aars2<+>	C57BL/6N-Aars2<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5756631	M	MP:0010068	decreased red blood cell distribution width	Aars2<tm1(KOMP)Wtsi>/Aars2<+>	C57BL/6N-Aars2<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5756632	F	MP:0001325	abnormal retina morphology	Abca1<tm1b(EUCOMM)Hmgu>/Abca1<+>	C57BL/6N-Abca1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5756634	M	MP:0005343	increased circulating aspartate transaminase level	Abca6<tm2b(KOMP)Wtsi>/Abca6<tm2b(KOMP)Wtsi>	C57BL/6N-Abca6<tm2b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756634	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Abca6<tm2b(KOMP)Wtsi>/Abca6<tm2b(KOMP)Wtsi>	C57BL/6N-Abca6<tm2b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756634	F	MP:0002608	increased hematocrit	Abca6<tm2b(KOMP)Wtsi>/Abca6<tm2b(KOMP)Wtsi>	C57BL/6N-Abca6<tm2b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756635	F	MP:0005343	increased circulating aspartate transaminase level	Abcb11<tm1b(EUCOMM)Hmgu>/Abcb11<+>	C57BL/6N-Abcb11<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756635	M	MP:0002644	decreased circulating triglyceride level	Abcb11<tm1b(EUCOMM)Hmgu>/Abcb11<+>	C57BL/6N-Abcb11<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756635	M	MP:0011896	increased circulating unsaturated transferrin level	Abcb11<tm1b(EUCOMM)Hmgu>/Abcb11<+>	C57BL/6N-Abcb11<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756635	M	MP:0008806	increased circulating amylase level	Abcb11<tm1b(EUCOMM)Hmgu>/Abcb11<+>	C57BL/6N-Abcb11<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756635	M	MP:0010087	increased circulating fructosamine level	Abcb11<tm1b(EUCOMM)Hmgu>/Abcb11<+>	C57BL/6N-Abcb11<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756635	M	MP:0005344	increased circulating bilirubin level	Abcb11<tm1b(EUCOMM)Hmgu>/Abcb11<+>	C57BL/6N-Abcb11<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756635	M	MP:0001175	abnormal lung morphology	Abcb11<tm1b(EUCOMM)Hmgu>/Abcb11<+>	C57BL/6N-Abcb11<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756637	M	MP:0003917	increased kidney weight	Abcc2<tm2b(KOMP)Wtsi>/Abcc2<tm2b(KOMP)Wtsi>	C57BL/6N-Abcc2<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756637	F	MP:0008935	decreased mean platelet volume	Abcc2<tm2b(KOMP)Wtsi>/Abcc2<tm2b(KOMP)Wtsi>	C57BL/6N-Abcc2<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756637	M	MP:0005016	decreased lymphocyte cell number	Abcc2<tm2b(KOMP)Wtsi>/Abcc2<tm2b(KOMP)Wtsi>	C57BL/6N-Abcc2<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756637	M	MP:0000219	increased neutrophil cell number	Abcc2<tm2b(KOMP)Wtsi>/Abcc2<tm2b(KOMP)Wtsi>	C57BL/6N-Abcc2<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756637	M	MP:0005343	increased circulating aspartate transaminase level	Abcc2<tm2b(KOMP)Wtsi>/Abcc2<tm2b(KOMP)Wtsi>	C57BL/6N-Abcc2<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756637	F	MP:0001556	increased circulating HDL cholesterol level	Abcc2<tm2b(KOMP)Wtsi>/Abcc2<tm2b(KOMP)Wtsi>	C57BL/6N-Abcc2<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756637	M	MP:0002941	increased circulating alanine transaminase level	Abcc2<tm2b(KOMP)Wtsi>/Abcc2<tm2b(KOMP)Wtsi>	C57BL/6N-Abcc2<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756638	F	MP:0001307	fused cornea and lens	Abcg2<tm1.1(KOMP)Vlcg>/Abcg2<+>	B6N(Cg)-Abcg2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756639	M	MP:0001556	increased circulating HDL cholesterol level	Abcg2<tm1.1(KOMP)Vlcg>/Abcg2<tm1.1(KOMP)Vlcg>	B6N(Cg)-Abcg2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756639	F	MP:0005566	decreased blood urea nitrogen level	Abcg2<tm1.1(KOMP)Vlcg>/Abcg2<tm1.1(KOMP)Vlcg>	B6N(Cg)-Abcg2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756640	F	MP:0002599	increased mean platelet volume	Abi3bp<tm1e.1(KOMP)Mbp>/Abi3bp<tm1e.1(KOMP)Mbp>	C57BL/6N-Abi3bp<tm1e.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5756640	F	MP:0010067	increased red blood cell distribution width	Abi3bp<tm1e.1(KOMP)Mbp>/Abi3bp<tm1e.1(KOMP)Mbp>	C57BL/6N-Abi3bp<tm1e.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5756640	M	MP:0002100	abnormal tooth morphology	Abi3bp<tm1e.1(KOMP)Mbp>/Abi3bp<tm1e.1(KOMP)Mbp>	C57BL/6N-Abi3bp<tm1e.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5756642	F	MP:0002590	increased mean corpuscular volume	Acbd3<tm1b(EUCOMM)Hmgu>/Acbd3<+>	C57BL/6N-Acbd3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756642	M	MP:0002644	decreased circulating triglyceride level	Acbd3<tm1b(EUCOMM)Hmgu>/Acbd3<+>	C57BL/6N-Acbd3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756642	F	MP:0005343	increased circulating aspartate transaminase level	Acbd3<tm1b(EUCOMM)Hmgu>/Acbd3<+>	C57BL/6N-Acbd3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756646	F	MP:0005560	decreased circulating glucose level	Acsm2<tm1.1(KOMP)Vlcg>/Acsm2<tm1.1(KOMP)Vlcg>	B6N(Cg)-Acsm2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756647	F	MP:0002875	decreased erythrocyte cell number	Actr8<tm1.1(KOMP)Vlcg>/Actr8<+>	B6N(Cg)-Actr8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756647	F	MP:0002874	decreased hemoglobin content	Actr8<tm1.1(KOMP)Vlcg>/Actr8<+>	B6N(Cg)-Actr8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756647	M	MP:0005633	increased circulating sodium level	Actr8<tm1.1(KOMP)Vlcg>/Actr8<+>	B6N(Cg)-Actr8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756647	F	MP:0000208	decreased hematocrit	Actr8<tm1.1(KOMP)Vlcg>/Actr8<+>	B6N(Cg)-Actr8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756649	F	MP:0001120	abnormal uterus morphology	Acvr1b<tm1.1(KOMP)Vlcg>/Acvr1b<+>	C57BL/6N-Acvr1b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5756649	M	MP:0001147	small testis	Acvr1b<tm1.1(KOMP)Vlcg>/Acvr1b<+>	C57BL/6N-Acvr1b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5756649	M	MP:0000367	abnormal coat/ hair morphology	Acvr1b<tm1.1(KOMP)Vlcg>/Acvr1b<+>	C57BL/6N-Acvr1b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5756649	M	MP:0000702	enlarged lymph nodes	Acvr1b<tm1.1(KOMP)Vlcg>/Acvr1b<+>	C57BL/6N-Acvr1b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5756649	M	MP:0002768	small adrenal glands	Acvr1b<tm1.1(KOMP)Vlcg>/Acvr1b<+>	C57BL/6N-Acvr1b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5756651	F	MP:0002100	abnormal tooth morphology	Adam23<tm1b(EUCOMM)Hmgu>/Adam23<+>	C57BL/6N-Adam23<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756655	F	MP:0001399	hyperactivity	Adck2<tm1.1(KOMP)Vlcg>/Adck2<tm1.1(KOMP)Vlcg>	B6N(Cg)-Adck2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756657	F	MP:0000063	decreased bone mineral density	Adgrd1<tm1b(EUCOMM)Wtsi>/Adgrd1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Adgrd1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756657	F	MP:0010124	decreased bone mineral content	Adgrd1<tm1b(EUCOMM)Wtsi>/Adgrd1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Adgrd1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756657	F	MP:0001926	female infertility	Adgrd1<tm1b(EUCOMM)Wtsi>/Adgrd1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Adgrd1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756658	M	MP:0010052	increased grip strength	Adgrf5<tm1b(KOMP)Wtsi>/Adgrf5<tm1b(KOMP)Wtsi>	C57BL/6N-Adgrf5<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756658	F	MP:0013279	increased fasting circulating glucose level	Adgrf5<tm1b(KOMP)Wtsi>/Adgrf5<tm1b(KOMP)Wtsi>	C57BL/6N-Adgrf5<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756658	F	MP:0000208	decreased hematocrit	Adgrf5<tm1b(KOMP)Wtsi>/Adgrf5<tm1b(KOMP)Wtsi>	C57BL/6N-Adgrf5<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756658	F	MP:0010124	decreased bone mineral content	Adgrf5<tm1b(KOMP)Wtsi>/Adgrf5<tm1b(KOMP)Wtsi>	C57BL/6N-Adgrf5<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756659	M	MP:0002764	short tibia	Adgrv1<tm1.1(KOMP)Vlcg>/Adgrv1<tm1.1(KOMP)Vlcg>	C57BL/6N-Adgrv1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5756659	M	MP:0001147	small testis	Adgrv1<tm1.1(KOMP)Vlcg>/Adgrv1<tm1.1(KOMP)Vlcg>	C57BL/6N-Adgrv1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5756659	M	MP:0001146	abnormal testis morphology	Adgrv1<tm1.1(KOMP)Vlcg>/Adgrv1<tm1.1(KOMP)Vlcg>	C57BL/6N-Adgrv1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5756660	M	MP:0001529	abnormal vocalization	Adh5<tm1b(EUCOMM)Wtsi>/Adh5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Adh5<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756661	M	MP:0005016	decreased lymphocyte cell number	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756661	M	MP:0002941	increased circulating alanine transaminase level	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756661	M	MP:0001566	increased circulating phosphate level	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756661	M	MP:0000219	increased neutrophil cell number	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756661	F	MP:0003921	abnormal heart left ventricle morphology	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756661	M	MP:0010067	increased red blood cell distribution width	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756661	F	MP:0005178	increased circulating cholesterol level	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756661	M	MP:0002874	decreased hemoglobin content	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756661	F	MP:0001556	increased circulating HDL cholesterol level	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756661	M	MP:0005565	increased blood urea nitrogen level	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756664	F	MP:0001297	microphthalmia	Adsl<tm1b(KOMP)Wtsi>/Adsl<+>	C57BL/6N-Adsl<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756667	F	MP:0010090	increased circulating creatine kinase level	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0010124	decreased bone mineral content	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0005178	increased circulating cholesterol level	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0005560	decreased circulating glucose level	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0010025	decreased total body fat amount	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0008806	increased circulating amylase level	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0003917	increased kidney weight	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0008810	increased circulating iron level	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0002941	increased circulating alanine transaminase level	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0000063	decreased bone mineral density	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0005293	impaired glucose tolerance	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0002968	increased circulating alkaline phosphatase level	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0005344	increased circulating bilirubin level	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	M	MP:0001406	abnormal gait	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0002833	increased heart weight	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0003960	increased lean body mass	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0013279	increased fasting circulating glucose level	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756667	F	MP:0005343	increased circulating aspartate transaminase level	Agl<tm1b(EUCOMM)Wtsi>/Agl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Agl<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756668	F	MP:0002968	increased circulating alkaline phosphatase level	Agpat1<tm1.1(KOMP)Vlcg>/Agpat1<+>	B6N(Cg)-Agpat1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756668	F	MP:0002959	increased urine microalbumin level	Agpat1<tm1.1(KOMP)Vlcg>/Agpat1<+>	B6N(Cg)-Agpat1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756668	M	MP:0005560	decreased circulating glucose level	Agpat1<tm1.1(KOMP)Vlcg>/Agpat1<+>	B6N(Cg)-Agpat1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756668	M	MP:0002941	increased circulating alanine transaminase level	Agpat1<tm1.1(KOMP)Vlcg>/Agpat1<+>	B6N(Cg)-Agpat1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756668	M	MP:0001759	increased urine glucose level	Agpat1<tm1.1(KOMP)Vlcg>/Agpat1<+>	B6N(Cg)-Agpat1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756668	F	MP:0005561	increased mean corpuscular hemoglobin	Agpat1<tm1.1(KOMP)Vlcg>/Agpat1<+>	B6N(Cg)-Agpat1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756668	F	MP:0010506	prolonged RR interval	Agpat1<tm1.1(KOMP)Vlcg>/Agpat1<+>	B6N(Cg)-Agpat1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756668	M	MP:0005627	increased circulating potassium level	Agpat1<tm1.1(KOMP)Vlcg>/Agpat1<+>	B6N(Cg)-Agpat1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756669	F	MP:0010124	decreased bone mineral content	Agpat4<tm1b(KOMP)Wtsi>/Agpat4<tm1b(KOMP)Wtsi>	C57BL/6N-Agpat4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756669	M	MP:0003961	decreased lean body mass	Agpat4<tm1b(KOMP)Wtsi>/Agpat4<tm1b(KOMP)Wtsi>	C57BL/6N-Agpat4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756669	F	MP:0003795	abnormal bone structure	Agpat4<tm1b(KOMP)Wtsi>/Agpat4<tm1b(KOMP)Wtsi>	C57BL/6N-Agpat4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756669	M	MP:0013279	increased fasting circulating glucose level	Agpat4<tm1b(KOMP)Wtsi>/Agpat4<tm1b(KOMP)Wtsi>	C57BL/6N-Agpat4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756670	M	MP:0002606	increased basophil cell number	Ahcy<tm1b(EUCOMM)Hmgu>/Ahcy<+>	C57BL/6N-Ahcy<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756670	M	MP:0010052	increased grip strength	Ahcy<tm1b(EUCOMM)Hmgu>/Ahcy<+>	C57BL/6N-Ahcy<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756672	M	MP:0005292	improved glucose tolerance	Ahnak<tm1b(KOMP)Mbp>/Ahnak<+>	C57BL/6N-Ahnak<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5756672	F	MP:0000220	increased monocyte cell number	Ahnak<tm1b(KOMP)Mbp>/Ahnak<+>	C57BL/6N-Ahnak<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5756672	F	MP:0012362	increased large unstained cell number	Ahnak<tm1b(KOMP)Mbp>/Ahnak<+>	C57BL/6N-Ahnak<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5756676	M	MP:0010025	decreased total body fat amount	Crybg1<tm1b(KOMP)Wtsi>/Crybg1<+>	C57BL/6N-Crybg1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756676	F	MP:0002092	abnormal eye morphology	Crybg1<tm1b(KOMP)Wtsi>/Crybg1<+>	C57BL/6N-Crybg1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756679	M	MP:0013278	decreased fasting circulating glucose level	Akr1b8<tm1.1(KOMP)Vlcg>/Akr1b8<tm1.1(KOMP)Vlcg>	B6N(Cg)-Akr1b8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756679	M	MP:0010052	increased grip strength	Akr1b8<tm1.1(KOMP)Vlcg>/Akr1b8<tm1.1(KOMP)Vlcg>	B6N(Cg)-Akr1b8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756679	F	MP:0005568	increased circulating total protein level	Akr1b8<tm1.1(KOMP)Vlcg>/Akr1b8<tm1.1(KOMP)Vlcg>	B6N(Cg)-Akr1b8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756681	M	MP:0001325	abnormal retina morphology	Aktip<tm1b(EUCOMM)Hmgu>/Aktip<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aktip<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756681	M	MP:0000063	decreased bone mineral density	Aktip<tm1b(EUCOMM)Hmgu>/Aktip<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aktip<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756681	M	MP:0005343	increased circulating aspartate transaminase level	Aktip<tm1b(EUCOMM)Hmgu>/Aktip<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aktip<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756681	M	MP:0010124	decreased bone mineral content	Aktip<tm1b(EUCOMM)Hmgu>/Aktip<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aktip<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756682	F	MP:0001303	abnormal lens morphology	Aldh1l1<tm1b(KOMP)Wtsi>/Aldh1l1<tm1b(KOMP)Wtsi>	C57BL/6N-Aldh1l1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756682	M	MP:0010097	abnormal retina blood vessel morphology	Aldh1l1<tm1b(KOMP)Wtsi>/Aldh1l1<tm1b(KOMP)Wtsi>	C57BL/6N-Aldh1l1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756682	F	MP:0001304	cataract	Aldh1l1<tm1b(KOMP)Wtsi>/Aldh1l1<tm1b(KOMP)Wtsi>	C57BL/6N-Aldh1l1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756684	M	MP:0003961	decreased lean body mass	Aldh3b1<tm1b(EUCOMM)Wtsi>/Aldh3b1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aldh3b1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756684	M	MP:0000063	decreased bone mineral density	Aldh3b1<tm1b(EUCOMM)Wtsi>/Aldh3b1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aldh3b1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756685	F	MP:0000063	decreased bone mineral density	Aldob<tm2b(EUCOMM)Wtsi>/Aldob<tm2b(EUCOMM)Wtsi>	C57BL/6N-Aldob<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756685	F	MP:0001258	decreased body length	Aldob<tm2b(EUCOMM)Wtsi>/Aldob<tm2b(EUCOMM)Wtsi>	C57BL/6N-Aldob<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756686	F	MP:0005533	increased body temperature	Alg10b<tm1(KOMP)Vlcg>/Alg10b<+>	C57BL/6N-Alg10b<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5756687	M	MP:0002079	increased circulating insulin level	Alg2<tm1.1(KOMP)Vlcg>/Alg2<+>	B6N(Cg)-Alg2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756687	M	MP:0013278	decreased fasting circulating glucose level	Alg2<tm1.1(KOMP)Vlcg>/Alg2<+>	B6N(Cg)-Alg2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756687	M	MP:0002110	abnormal digit morphology	Alg2<tm1.1(KOMP)Vlcg>/Alg2<+>	B6N(Cg)-Alg2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756690	M	MP:0000222	decreased neutrophil cell number	Ampd1<tm1b(KOMP)Wtsi>/Ampd1<+>	C57BL/6N-Ampd1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756690	F	MP:0002599	increased mean platelet volume	Ampd1<tm1b(KOMP)Wtsi>/Ampd1<+>	C57BL/6N-Ampd1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756692	M	MP:0001556	increased circulating HDL cholesterol level	Anapc15<tm1.1(KOMP)Vlcg>/Anapc15<+>	B6N(Cg)-Anapc15<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756693	F	MP:0011495	abnormal head shape	Anapc15<tm1.1(KOMP)Vlcg>/Anapc15<tm1.1(KOMP)Vlcg>	B6N(Cg)-Anapc15<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756693	M	MP:0001711	abnormal placenta morphology	Anapc15<tm1.1(KOMP)Vlcg>/Anapc15<tm1.1(KOMP)Vlcg>	B6N(Cg)-Anapc15<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756693	M	MP:0000841	abnormal hindbrain morphology	Anapc15<tm1.1(KOMP)Vlcg>/Anapc15<tm1.1(KOMP)Vlcg>	B6N(Cg)-Anapc15<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756693	F	MP:0011239	abnormal skin coloration	Anapc15<tm1.1(KOMP)Vlcg>/Anapc15<tm1.1(KOMP)Vlcg>	B6N(Cg)-Anapc15<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756693	M	MP:0000783	abnormal forebrain morphology	Anapc15<tm1.1(KOMP)Vlcg>/Anapc15<tm1.1(KOMP)Vlcg>	B6N(Cg)-Anapc15<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756693	M	MP:0003717	pallor	Anapc15<tm1.1(KOMP)Vlcg>/Anapc15<tm1.1(KOMP)Vlcg>	B6N(Cg)-Anapc15<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756693	F	MP:0001297	microphthalmia	Anapc15<tm1.1(KOMP)Vlcg>/Anapc15<tm1.1(KOMP)Vlcg>	B6N(Cg)-Anapc15<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756693	M	MP:0000897	abnormal midbrain morphology	Anapc15<tm1.1(KOMP)Vlcg>/Anapc15<tm1.1(KOMP)Vlcg>	B6N(Cg)-Anapc15<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756696	F	MP:0005178	increased circulating cholesterol level	Ankrd11<tm1b(EUCOMM)Wtsi>/Ankrd11<+>	C57BL/6N-Ankrd11<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5756696	F	MP:0001556	increased circulating HDL cholesterol level	Ankrd11<tm1b(EUCOMM)Wtsi>/Ankrd11<+>	C57BL/6N-Ankrd11<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5756696	F	MP:0002699	abnormal vitreous body morphology	Ankrd11<tm1b(EUCOMM)Wtsi>/Ankrd11<+>	C57BL/6N-Ankrd11<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5756696	F	MP:0001486	abnormal startle reflex	Ankrd11<tm1b(EUCOMM)Wtsi>/Ankrd11<+>	C57BL/6N-Ankrd11<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5756696	F	MP:0001258	decreased body length	Ankrd11<tm1b(EUCOMM)Wtsi>/Ankrd11<+>	C57BL/6N-Ankrd11<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5756698	M	MP:0002764	short tibia	Ankrd27<tm1b(EUCOMM)Hmgu>/Ankrd27<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ankrd27<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756703	M	MP:0000198	decreased circulating phosphate level	Aoc1<tm1b(EUCOMM)Hmgu>/Aoc1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aoc1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756703	M	MP:0002941	increased circulating alanine transaminase level	Aoc1<tm1b(EUCOMM)Hmgu>/Aoc1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aoc1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756703	F	MP:0001303	abnormal lens morphology	Aoc1<tm1b(EUCOMM)Hmgu>/Aoc1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aoc1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756704	F	MP:0001554	increased circulating free fatty acids level	Ap2a2<tm1b(EUCOMM)Wtsi>/Ap2a2<+>	C57BL/6N-Ap2a2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756705	F	MP:0002968	increased circulating alkaline phosphatase level	Ap2a2<tm1b(EUCOMM)Wtsi>/Ap2a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap2a2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756705	F	MP:0005178	increased circulating cholesterol level	Ap2a2<tm1b(EUCOMM)Wtsi>/Ap2a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap2a2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756705	F	MP:0008810	increased circulating iron level	Ap2a2<tm1b(EUCOMM)Wtsi>/Ap2a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap2a2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756705	F	MP:0006358	absent pinna reflex	Ap2a2<tm1b(EUCOMM)Wtsi>/Ap2a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap2a2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756705	F	MP:0005419	decreased circulating serum albumin level	Ap2a2<tm1b(EUCOMM)Wtsi>/Ap2a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap2a2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756705	F	MP:0000182	increased circulating LDL cholesterol level	Ap2a2<tm1b(EUCOMM)Wtsi>/Ap2a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap2a2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756705	F	MP:0010088	decreased circulating fructosamine level	Ap2a2<tm1b(EUCOMM)Wtsi>/Ap2a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap2a2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756705	F	MP:0005562	decreased mean corpuscular hemoglobin	Ap2a2<tm1b(EUCOMM)Wtsi>/Ap2a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap2a2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756705	F	MP:0001556	increased circulating HDL cholesterol level	Ap2a2<tm1b(EUCOMM)Wtsi>/Ap2a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap2a2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756706	M	MP:0013279	increased fasting circulating glucose level	Ap3s1<tm1b(EUCOMM)Hmgu>/Ap3s1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ap3s1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756706	M	MP:0002968	increased circulating alkaline phosphatase level	Ap3s1<tm1b(EUCOMM)Hmgu>/Ap3s1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ap3s1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756707	M	MP:0001399	hyperactivity	Ap3s2<tm1b(EUCOMM)Hmgu>/Ap3s2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ap3s2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5756707	M	MP:0020870	decreased thigmotaxis	Ap3s2<tm1b(EUCOMM)Hmgu>/Ap3s2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ap3s2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5756707	M	MP:0004924	abnormal behavior	Ap3s2<tm1b(EUCOMM)Hmgu>/Ap3s2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ap3s2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5756707	M	MP:0001364	decreased anxiety-related response	Ap3s2<tm1b(EUCOMM)Hmgu>/Ap3s2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ap3s2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5756707	M	MP:0001402	decreased locomotor activity	Ap3s2<tm1b(EUCOMM)Hmgu>/Ap3s2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ap3s2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5756708	M	MP:0003917	increased kidney weight	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756708	F	MP:0005343	increased circulating aspartate transaminase level	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756708	M	MP:0010090	increased circulating creatine kinase level	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756708	F	MP:0010379	decreased respiratory quotient	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756708	M	MP:0002608	increased hematocrit	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756708	F	MP:0010052	increased grip strength	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756709	F	MP:0001415	increased exploration in new environment	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756709	M	MP:0008806	increased circulating amylase level	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756709	M	MP:0005599	increased cardiac muscle contractility	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756709	F	MP:0005293	impaired glucose tolerance	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756710	F	MP:0003393	decreased cardiac output	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756710	F	MP:0005333	decreased heart rate	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756710	F	MP:0003733	abnormal retina inner nuclear layer morphology	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756710	F	MP:0000689	abnormal spleen morphology	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756711	M	MP:0020870	decreased thigmotaxis	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756711	M	MP:0004924	abnormal behavior	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756711	M	MP:0005560	decreased circulating glucose level	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756712	F	MP:0004122	abnormal sinus arrhythmia	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756712	M	MP:0003960	increased lean body mass	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756712	M	MP:0002833	increased heart weight	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756712	F	MP:0003929	decreased heart rate variability	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756712	M	MP:0010123	increased bone mineral content	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756712	F	MP:0000702	enlarged lymph nodes	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756712	M	MP:0001488	increased startle reflex	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756712	F	MP:0005385	cardiovascular system phenotype	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756712	M	MP:0009454	impaired contextual conditioning behavior	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756712	M	MP:0020420	abnormal freezing behavior	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756713	M	MP:0010053	decreased grip strength	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:5756714	F	MP:0005419	decreased circulating serum albumin level	Ap4m1<tm1b(EUCOMM)Wtsi>/Ap4m1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap4m1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756714	M	MP:0002608	increased hematocrit	Ap4m1<tm1b(EUCOMM)Wtsi>/Ap4m1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap4m1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756714	F	MP:0008810	increased circulating iron level	Ap4m1<tm1b(EUCOMM)Wtsi>/Ap4m1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap4m1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756714	M	MP:0000218	increased leukocyte cell number	Ap4m1<tm1b(EUCOMM)Wtsi>/Ap4m1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap4m1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756714	F	MP:0002968	increased circulating alkaline phosphatase level	Ap4m1<tm1b(EUCOMM)Wtsi>/Ap4m1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap4m1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756714	F	MP:0005343	increased circulating aspartate transaminase level	Ap4m1<tm1b(EUCOMM)Wtsi>/Ap4m1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap4m1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756714	F	MP:0002941	increased circulating alanine transaminase level	Ap4m1<tm1b(EUCOMM)Wtsi>/Ap4m1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ap4m1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756715	M	MP:0009141	increased prepulse inhibition	Aph1c<tm1b(KOMP)Wtsi>/Aph1c<tm1b(KOMP)Wtsi>	C57BL/6N-Aph1c<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756715	M	MP:0002075	abnormal coat/hair pigmentation	Aph1c<tm1b(KOMP)Wtsi>/Aph1c<tm1b(KOMP)Wtsi>	C57BL/6N-Aph1c<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756716	M	MP:0005419	decreased circulating serum albumin level	Apip<tm1b(EUCOMM)Wtsi>/Apip<tm1b(EUCOMM)Wtsi>	C57BL/6N-Apip<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756717	M	MP:0002764	short tibia	Aplp2<tm2b(EUCOMM)Hmgu>/Aplp2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Aplp2<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5756717	F	MP:0002591	decreased mean corpuscular volume	Aplp2<tm2b(EUCOMM)Hmgu>/Aplp2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Aplp2<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5756717	F	MP:0000063	decreased bone mineral density	Aplp2<tm2b(EUCOMM)Hmgu>/Aplp2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Aplp2<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5756718	F	MP:0011965	decreased total retina thickness	App<tm1b(KOMP)Wtsi>/App<+>	C57BL/6N-App<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5756718	M	MP:0005565	increased blood urea nitrogen level	App<tm1b(KOMP)Wtsi>/App<+>	C57BL/6N-App<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5756718	M	MP:0011962	increased cornea thickness	App<tm1b(KOMP)Wtsi>/App<+>	C57BL/6N-App<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5756719	F	MP:0005565	increased blood urea nitrogen level	Aqp3<tm2b(EUCOMM)Wtsi>/Aqp3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Aqp3<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756719	F	MP:0005568	increased circulating total protein level	Aqp3<tm2b(EUCOMM)Wtsi>/Aqp3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Aqp3<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756719	F	MP:0005178	increased circulating cholesterol level	Aqp3<tm2b(EUCOMM)Wtsi>/Aqp3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Aqp3<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756719	F	MP:0005553	increased circulating creatinine level	Aqp3<tm2b(EUCOMM)Wtsi>/Aqp3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Aqp3<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756719	F	MP:0001556	increased circulating HDL cholesterol level	Aqp3<tm2b(EUCOMM)Wtsi>/Aqp3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Aqp3<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756719	F	MP:0002968	increased circulating alkaline phosphatase level	Aqp3<tm2b(EUCOMM)Wtsi>/Aqp3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Aqp3<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756719	F	MP:0003960	increased lean body mass	Aqp3<tm2b(EUCOMM)Wtsi>/Aqp3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Aqp3<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756719	F	MP:0002965	increased circulating serum albumin level	Aqp3<tm2b(EUCOMM)Wtsi>/Aqp3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Aqp3<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756720	F	MP:0011964	increased total retina thickness	Aqp6<tm1b(EUCOMM)Hmgu>/Aqp6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aqp6<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756720	F	MP:0002135	abnormal kidney morphology	Aqp6<tm1b(EUCOMM)Hmgu>/Aqp6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aqp6<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756720	M	MP:0003019	increased circulating chloride level	Aqp6<tm1b(EUCOMM)Hmgu>/Aqp6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aqp6<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756721	M	MP:0013278	decreased fasting circulating glucose level	Arf2<tm1.1(KOMP)Wtsi>/Arf2<tm1.1(KOMP)Wtsi>	B6N(Cg)-Arf2<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756721	M	MP:0010052	increased grip strength	Arf2<tm1.1(KOMP)Wtsi>/Arf2<tm1.1(KOMP)Wtsi>	B6N(Cg)-Arf2<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756721	F	MP:0003795	abnormal bone structure	Arf2<tm1.1(KOMP)Wtsi>/Arf2<tm1.1(KOMP)Wtsi>	B6N(Cg)-Arf2<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756722	F	MP:0005419	decreased circulating serum albumin level	Arhgap23<tm1b(EUCOMM)Wtsi>/Arhgap23<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arhgap23<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756722	F	MP:0000198	decreased circulating phosphate level	Arhgap23<tm1b(EUCOMM)Wtsi>/Arhgap23<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arhgap23<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756723	M	MP:0001402	decreased locomotor activity	Arhgap24<tm1b(KOMP)Wtsi>/Arhgap24<tm1b(KOMP)Wtsi>	C57BL/6N-Arhgap24<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5756727	M	MP:0002875	decreased erythrocyte cell number	Arid3a<tm1b(KOMP)Wtsi>/Arid3a<+>	B6N(Cg)-Arid3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756727	M	MP:0001552	increased circulating triglyceride level	Arid3a<tm1b(KOMP)Wtsi>/Arid3a<+>	B6N(Cg)-Arid3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756727	M	MP:0002874	decreased hemoglobin content	Arid3a<tm1b(KOMP)Wtsi>/Arid3a<+>	B6N(Cg)-Arid3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756727	M	MP:0002079	increased circulating insulin level	Arid3a<tm1b(KOMP)Wtsi>/Arid3a<+>	B6N(Cg)-Arid3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756727	M	MP:0000208	decreased hematocrit	Arid3a<tm1b(KOMP)Wtsi>/Arid3a<+>	B6N(Cg)-Arid3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756731	M	MP:0003179	thrombocytopenia	Arrb1<tm1b(KOMP)Wtsi>/Arrb1<tm1b(KOMP)Wtsi>	B6N(Cg)-Arrb1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756731	M	MP:0001488	increased startle reflex	Arrb1<tm1b(KOMP)Wtsi>/Arrb1<tm1b(KOMP)Wtsi>	B6N(Cg)-Arrb1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756731	M	MP:0009142	decreased prepulse inhibition	Arrb1<tm1b(KOMP)Wtsi>/Arrb1<tm1b(KOMP)Wtsi>	B6N(Cg)-Arrb1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756736	M	MP:0010580	decreased heart left ventricle size	Ascc2<tm1b(EUCOMM)Wtsi>/Ascc2<+>	C57BL/6N-Ascc2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756738	F	MP:0002591	decreased mean corpuscular volume	Aspn<tm1b(EUCOMM)Hmgu>/Aspn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aspn<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756739	M	MP:0001417	decreased exploration in new environment	Atad2b<tm1b(EUCOMM)Hmgu>/Atad2b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atad2b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756739	F	MP:0002135	abnormal kidney morphology	Atad2b<tm1b(EUCOMM)Hmgu>/Atad2b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atad2b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756739	M	MP:0004357	long tibia	Atad2b<tm1b(EUCOMM)Hmgu>/Atad2b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atad2b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756739	F	MP:0001399	hyperactivity	Atad2b<tm1b(EUCOMM)Hmgu>/Atad2b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atad2b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756739	M	MP:0008040	decreased NK T cell number	Atad2b<tm1b(EUCOMM)Hmgu>/Atad2b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atad2b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756739	M	MP:0000186	decreased circulating HDL cholesterol level	Atad2b<tm1b(EUCOMM)Hmgu>/Atad2b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atad2b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756739	M	MP:0005179	decreased circulating cholesterol level	Atad2b<tm1b(EUCOMM)Hmgu>/Atad2b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atad2b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756742	F	MP:0001304	cataract	Atn1<tm1b(EUCOMM)Wtsi>/Atn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atn1<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756742	F	MP:0001552	increased circulating triglyceride level	Atn1<tm1b(EUCOMM)Wtsi>/Atn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atn1<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756742	F	MP:0002875	decreased erythrocyte cell number	Atn1<tm1b(EUCOMM)Wtsi>/Atn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atn1<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756742	F	MP:0001417	decreased exploration in new environment	Atn1<tm1b(EUCOMM)Wtsi>/Atn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atn1<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756742	M	MP:0005016	decreased lymphocyte cell number	Atn1<tm1b(EUCOMM)Wtsi>/Atn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atn1<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756742	F	MP:0005385	cardiovascular system phenotype	Atn1<tm1b(EUCOMM)Wtsi>/Atn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atn1<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756742	M	MP:0000266	abnormal heart morphology	Atn1<tm1b(EUCOMM)Wtsi>/Atn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atn1<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756742	F	MP:0001406	abnormal gait	Atn1<tm1b(EUCOMM)Wtsi>/Atn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atn1<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756742	M	MP:0000219	increased neutrophil cell number	Atn1<tm1b(EUCOMM)Wtsi>/Atn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atn1<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756742	M	MP:0005419	decreased circulating serum albumin level	Atn1<tm1b(EUCOMM)Wtsi>/Atn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atn1<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756743	F	MP:0001364	decreased anxiety-related response	Atp1a3<tm1b(EUCOMM)Hmgu>/Atp1a3<+>	C57BL/6N-Atp1a3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756743	F	MP:0001415	increased exploration in new environment	Atp1a3<tm1b(EUCOMM)Hmgu>/Atp1a3<+>	C57BL/6N-Atp1a3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756743	M	MP:0005292	improved glucose tolerance	Atp1a3<tm1b(EUCOMM)Hmgu>/Atp1a3<+>	C57BL/6N-Atp1a3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756743	F	MP:0001399	hyperactivity	Atp1a3<tm1b(EUCOMM)Hmgu>/Atp1a3<+>	C57BL/6N-Atp1a3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756745	M	MP:0001925	male infertility	Atp1a4<tm1b(KOMP)Wtsi>/Atp1a4<tm1b(KOMP)Wtsi>	C57BL/6N-Atp1a4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756748	M	MP:0013279	increased fasting circulating glucose level	Atp2a2<tm1b(EUCOMM)Hmgu>/Atp2a2<+>	C57BL/6N-Atp2a2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756748	F	MP:0002966	decreased circulating alkaline phosphatase level	Atp2a2<tm1b(EUCOMM)Hmgu>/Atp2a2<+>	C57BL/6N-Atp2a2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756748	F	MP:0008935	decreased mean platelet volume	Atp2a2<tm1b(EUCOMM)Hmgu>/Atp2a2<+>	C57BL/6N-Atp2a2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756750	M	MP:0002631	abnormal epididymis morphology	Atp2b1<tm1b(KOMP)Wtsi>/Atp2b1<+>	C57BL/6N-Atp2b1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756750	F	MP:0001284	absent vibrissae	Atp2b1<tm1b(KOMP)Wtsi>/Atp2b1<+>	C57BL/6N-Atp2b1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756750	M	MP:0004931	enlarged epididymis	Atp2b1<tm1b(KOMP)Wtsi>/Atp2b1<+>	C57BL/6N-Atp2b1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756750	F	MP:0002098	abnormal vibrissa morphology	Atp2b1<tm1b(KOMP)Wtsi>/Atp2b1<+>	C57BL/6N-Atp2b1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756751	F	MP:0011100	preweaning lethality, complete penetrance	Atp2b1<tm1b(KOMP)Wtsi>/Atp2b1<tm1b(KOMP)Wtsi>	C57BL/6N-Atp2b1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756754	M	MP:0001325	abnormal retina morphology	Atp5mc2<tm2b(EUCOMM)Hmgu>/Atp5mc2<+>	C57BL/6N-Atp5mc2<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756754	M	MP:0013279	increased fasting circulating glucose level	Atp5mc2<tm2b(EUCOMM)Hmgu>/Atp5mc2<+>	C57BL/6N-Atp5mc2<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756756	M	MP:0005565	increased blood urea nitrogen level	Atp5mg<tm1b(EUCOMM)Hmgu>/Atp5mg<+>	C57BL/6N-Atp5mg<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756756	M	MP:0005012	decreased eosinophil cell number	Atp5mg<tm1b(EUCOMM)Hmgu>/Atp5mg<+>	C57BL/6N-Atp5mg<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756756	F	MP:0000691	enlarged spleen	Atp5mg<tm1b(EUCOMM)Hmgu>/Atp5mg<+>	C57BL/6N-Atp5mg<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756756	M	MP:0005561	increased mean corpuscular hemoglobin	Atp5mg<tm1b(EUCOMM)Hmgu>/Atp5mg<+>	C57BL/6N-Atp5mg<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756756	F	MP:0000274	enlarged heart	Atp5mg<tm1b(EUCOMM)Hmgu>/Atp5mg<+>	C57BL/6N-Atp5mg<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756756	M	MP:0002965	increased circulating serum albumin level	Atp5mg<tm1b(EUCOMM)Hmgu>/Atp5mg<+>	C57BL/6N-Atp5mg<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756758	M	MP:0010123	increased bone mineral content	Atp6v0a1<tm1b(EUCOMM)Hmgu>/Atp6v0a1<+>	C57BL/6N-Atp6v0a1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756758	M	MP:0010025	decreased total body fat amount	Atp6v0a1<tm1b(EUCOMM)Hmgu>/Atp6v0a1<+>	C57BL/6N-Atp6v0a1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756758	F	MP:0005627	increased circulating potassium level	Atp6v0a1<tm1b(EUCOMM)Hmgu>/Atp6v0a1<+>	C57BL/6N-Atp6v0a1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756761	M	MP:0005016	decreased lymphocyte cell number	Atp6v0d1<tm1b(EUCOMM)Hmgu>/Atp6v0d1<+>	C57BL/6N-Atp6v0d1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756761	M	MP:0000219	increased neutrophil cell number	Atp6v0d1<tm1b(EUCOMM)Hmgu>/Atp6v0d1<+>	C57BL/6N-Atp6v0d1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756761	M	MP:0002059	abnormal seminal vesicle morphology	Atp6v0d1<tm1b(EUCOMM)Hmgu>/Atp6v0d1<+>	C57BL/6N-Atp6v0d1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756761	F	MP:0002764	short tibia	Atp6v0d1<tm1b(EUCOMM)Hmgu>/Atp6v0d1<+>	C57BL/6N-Atp6v0d1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756761	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Atp6v0d1<tm1b(EUCOMM)Hmgu>/Atp6v0d1<+>	C57BL/6N-Atp6v0d1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756761	M	MP:0002135	abnormal kidney morphology	Atp6v0d1<tm1b(EUCOMM)Hmgu>/Atp6v0d1<+>	C57BL/6N-Atp6v0d1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756763	M	MP:0002874	decreased hemoglobin content	Atp6v1b2<tm1b(KOMP)Wtsi>/Atp6v1b2<+>	C57BL/6N-Atp6v1b2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756763	M	MP:0002217	small lymph nodes	Atp6v1b2<tm1b(KOMP)Wtsi>/Atp6v1b2<+>	C57BL/6N-Atp6v1b2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756763	F	MP:0002591	decreased mean corpuscular volume	Atp6v1b2<tm1b(KOMP)Wtsi>/Atp6v1b2<+>	C57BL/6N-Atp6v1b2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756763	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Atp6v1b2<tm1b(KOMP)Wtsi>/Atp6v1b2<+>	C57BL/6N-Atp6v1b2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756763	F	MP:0002968	increased circulating alkaline phosphatase level	Atp6v1b2<tm1b(KOMP)Wtsi>/Atp6v1b2<+>	C57BL/6N-Atp6v1b2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756765	F	MP:0004122	abnormal sinus arrhythmia	Atp6v1d<tm1b(EUCOMM)Hmgu>/Atp6v1d<+>	C57BL/6N-Atp6v1d<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756765	F	MP:0005385	cardiovascular system phenotype	Atp6v1d<tm1b(EUCOMM)Hmgu>/Atp6v1d<+>	C57BL/6N-Atp6v1d<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756765	M	MP:0008935	decreased mean platelet volume	Atp6v1d<tm1b(EUCOMM)Hmgu>/Atp6v1d<+>	C57BL/6N-Atp6v1d<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756765	F	MP:0003928	increased heart rate variability	Atp6v1d<tm1b(EUCOMM)Hmgu>/Atp6v1d<+>	C57BL/6N-Atp6v1d<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756765	M	MP:0003960	increased lean body mass	Atp6v1d<tm1b(EUCOMM)Hmgu>/Atp6v1d<+>	C57BL/6N-Atp6v1d<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756765	M	MP:0005505	thrombocytosis	Atp6v1d<tm1b(EUCOMM)Hmgu>/Atp6v1d<+>	C57BL/6N-Atp6v1d<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756772	M	MP:0002075	abnormal coat/hair pigmentation	Atxn7l3<tm1.1(KOMP)Wtsi>/Atxn7l3<+>	C57BL/6N-Atxn7l3<tm1.1(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5756772	M	MP:0002792	abnormal retina vasculature morphology	Atxn7l3<tm1.1(KOMP)Wtsi>/Atxn7l3<+>	C57BL/6N-Atxn7l3<tm1.1(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5756772	M	MP:0010097	abnormal retina blood vessel morphology	Atxn7l3<tm1.1(KOMP)Wtsi>/Atxn7l3<+>	C57BL/6N-Atxn7l3<tm1.1(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5756772	M	MP:0011965	decreased total retina thickness	Atxn7l3<tm1.1(KOMP)Wtsi>/Atxn7l3<+>	C57BL/6N-Atxn7l3<tm1.1(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5756774	M	MP:0005013	increased lymphocyte cell number	Avp<tm1b(EUCOMM)Wtsi>/Avp<+>	C57BL/6N-Avp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756774	M	MP:0005568	increased circulating total protein level	Avp<tm1b(EUCOMM)Wtsi>/Avp<+>	C57BL/6N-Avp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756774	M	MP:0000222	decreased neutrophil cell number	Avp<tm1b(EUCOMM)Wtsi>/Avp<+>	C57BL/6N-Avp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756774	M	MP:0012361	decreased large unstained cell number	Avp<tm1b(EUCOMM)Wtsi>/Avp<+>	C57BL/6N-Avp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756774	F	MP:0001523	impaired righting response	Avp<tm1b(EUCOMM)Wtsi>/Avp<+>	C57BL/6N-Avp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756779	F	MP:0005566	decreased blood urea nitrogen level	Bag3<tm1b(EUCOMM)Hmgu>/Bag3<+>	C57BL/6N-Bag3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756781	F	MP:0005344	increased circulating bilirubin level	Baiap2l2<tm1a(EUCOMM)Hmgu>/Baiap2l2<tm1a(EUCOMM)Hmgu>	C57BL/6N-Baiap2l2<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756781	M	MP:0010053	decreased grip strength	Baiap2l2<tm1a(EUCOMM)Hmgu>/Baiap2l2<tm1a(EUCOMM)Hmgu>	C57BL/6N-Baiap2l2<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756781	F	MP:0009142	decreased prepulse inhibition	Baiap2l2<tm1a(EUCOMM)Hmgu>/Baiap2l2<tm1a(EUCOMM)Hmgu>	C57BL/6N-Baiap2l2<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756782	F	MP:0001406	abnormal gait	Baiap2l2<tm1b(EUCOMM)Hmgu>/Baiap2l2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Baiap2l2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756782	M	MP:0001489	decreased startle reflex	Baiap2l2<tm1b(EUCOMM)Hmgu>/Baiap2l2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Baiap2l2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756782	M	MP:0001486	abnormal startle reflex	Baiap2l2<tm1b(EUCOMM)Hmgu>/Baiap2l2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Baiap2l2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756784	F	MP:0010090	increased circulating creatine kinase level	Barx2<tm1b(EUCOMM)Hmgu>/Barx2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Barx2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756784	F	MP:0008806	increased circulating amylase level	Barx2<tm1b(EUCOMM)Hmgu>/Barx2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Barx2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756784	F	MP:0005343	increased circulating aspartate transaminase level	Barx2<tm1b(EUCOMM)Hmgu>/Barx2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Barx2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756784	F	MP:0002092	abnormal eye morphology	Barx2<tm1b(EUCOMM)Hmgu>/Barx2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Barx2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756784	M	MP:0002075	abnormal coat/hair pigmentation	Barx2<tm1b(EUCOMM)Hmgu>/Barx2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Barx2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756784	M	MP:0002111	abnormal tail morphology	Barx2<tm1b(EUCOMM)Hmgu>/Barx2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Barx2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756784	M	MP:0001406	abnormal gait	Barx2<tm1b(EUCOMM)Hmgu>/Barx2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Barx2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756784	M	MP:0005344	increased circulating bilirubin level	Barx2<tm1b(EUCOMM)Hmgu>/Barx2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Barx2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756784	M	MP:0001284	absent vibrissae	Barx2<tm1b(EUCOMM)Hmgu>/Barx2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Barx2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756785	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Baz1a<tm1b(EUCOMM)Hmgu>/Baz1a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Baz1a<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756785	F	MP:0005562	decreased mean corpuscular hemoglobin	Baz1a<tm1b(EUCOMM)Hmgu>/Baz1a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Baz1a<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756785	M	MP:0010052	increased grip strength	Baz1a<tm1b(EUCOMM)Hmgu>/Baz1a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Baz1a<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756785	M	MP:0000470	abnormal stomach morphology	Baz1a<tm1b(EUCOMM)Hmgu>/Baz1a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Baz1a<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756785	M	MP:0001925	male infertility	Baz1a<tm1b(EUCOMM)Hmgu>/Baz1a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Baz1a<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756786	F	MP:0000783	abnormal forebrain morphology	Bbox1<tm1b(KOMP)Wtsi>/Bbox1<tm1b(KOMP)Wtsi>	C57BL/6N-Bbox1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756786	F	MP:0000428	abnormal craniofacial morphology	Bbox1<tm1b(KOMP)Wtsi>/Bbox1<tm1b(KOMP)Wtsi>	C57BL/6N-Bbox1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756786	F	MP:0003720	abnormal neural tube closure	Bbox1<tm1b(KOMP)Wtsi>/Bbox1<tm1b(KOMP)Wtsi>	C57BL/6N-Bbox1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756786	F	MP:0000841	abnormal hindbrain morphology	Bbox1<tm1b(KOMP)Wtsi>/Bbox1<tm1b(KOMP)Wtsi>	C57BL/6N-Bbox1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756786	F	MP:0000897	abnormal midbrain morphology	Bbox1<tm1b(KOMP)Wtsi>/Bbox1<tm1b(KOMP)Wtsi>	C57BL/6N-Bbox1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756787	M	MP:0005633	increased circulating sodium level	Bbs10<tm1.1(KOMP)Vlcg>/Bbs10<+>	B6N(Cg)-Bbs10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756790	M	MP:0001325	abnormal retina morphology	Bbs5<tm1b(EUCOMM)Wtsi>/Bbs5<tm1b(EUCOMM)Wtsi>	C57BL/6NTac-Bbs5<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756790	F	MP:0002644	decreased circulating triglyceride level	Bbs5<tm1b(EUCOMM)Wtsi>/Bbs5<tm1b(EUCOMM)Wtsi>	C57BL/6NTac-Bbs5<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756790	M	MP:0010087	increased circulating fructosamine level	Bbs5<tm1b(EUCOMM)Wtsi>/Bbs5<tm1b(EUCOMM)Wtsi>	C57BL/6NTac-Bbs5<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756790	M	MP:0000745	tremors	Bbs5<tm1b(EUCOMM)Wtsi>/Bbs5<tm1b(EUCOMM)Wtsi>	C57BL/6NTac-Bbs5<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756790	F	MP:0005564	increased hemoglobin content	Bbs5<tm1b(EUCOMM)Wtsi>/Bbs5<tm1b(EUCOMM)Wtsi>	C57BL/6NTac-Bbs5<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756790	M	MP:0010379	decreased respiratory quotient	Bbs5<tm1b(EUCOMM)Wtsi>/Bbs5<tm1b(EUCOMM)Wtsi>	C57BL/6NTac-Bbs5<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756790	F	MP:0010053	decreased grip strength	Bbs5<tm1b(EUCOMM)Wtsi>/Bbs5<tm1b(EUCOMM)Wtsi>	C57BL/6NTac-Bbs5<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756790	F	MP:0003795	abnormal bone structure	Bbs5<tm1b(EUCOMM)Wtsi>/Bbs5<tm1b(EUCOMM)Wtsi>	C57BL/6NTac-Bbs5<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756790	M	MP:0003179	thrombocytopenia	Bbs5<tm1b(EUCOMM)Wtsi>/Bbs5<tm1b(EUCOMM)Wtsi>	C57BL/6NTac-Bbs5<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756790	M	MP:0001406	abnormal gait	Bbs5<tm1b(EUCOMM)Wtsi>/Bbs5<tm1b(EUCOMM)Wtsi>	C57BL/6NTac-Bbs5<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756790	F	MP:0002608	increased hematocrit	Bbs5<tm1b(EUCOMM)Wtsi>/Bbs5<tm1b(EUCOMM)Wtsi>	C57BL/6NTac-Bbs5<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756793	F	MP:0005179	decreased circulating cholesterol level	Kics2<tm1b(KOMP)Wtsi>/Kics2<tm1b(KOMP)Wtsi>	C57BL/6N-Kics2<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5756793	F	MP:0000198	decreased circulating phosphate level	Kics2<tm1b(KOMP)Wtsi>/Kics2<tm1b(KOMP)Wtsi>	C57BL/6N-Kics2<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5756793	F	MP:0000186	decreased circulating HDL cholesterol level	Kics2<tm1b(KOMP)Wtsi>/Kics2<tm1b(KOMP)Wtsi>	C57BL/6N-Kics2<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5756793	F	MP:0005565	increased blood urea nitrogen level	Kics2<tm1b(KOMP)Wtsi>/Kics2<tm1b(KOMP)Wtsi>	C57BL/6N-Kics2<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5756794	M	MP:0008806	increased circulating amylase level	Firrm<tm1b(EUCOMM)Hmgu>/Firrm<+>	C57BL/6N-Firrm<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756794	M	MP:0004509	abnormal pelvic girdle bone morphology	Firrm<tm1b(EUCOMM)Hmgu>/Firrm<+>	C57BL/6N-Firrm<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756797	M	MP:0001488	increased startle reflex	Bex2<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Bex2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756797	M	MP:0001402	decreased locomotor activity	Bex2<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Bex2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756797	M	MP:0001303	abnormal lens morphology	Bex2<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Bex2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756797	M	MP:0001325	abnormal retina morphology	Bex2<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Bex2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756798	F	MP:0009142	decreased prepulse inhibition	Bex2<tm1b(EUCOMM)Hmgu>/Bex2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bex2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756798	F	MP:0001488	increased startle reflex	Bex2<tm1b(EUCOMM)Hmgu>/Bex2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bex2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756798	F	MP:0001402	decreased locomotor activity	Bex2<tm1b(EUCOMM)Hmgu>/Bex2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bex2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756798	F	MP:0002075	abnormal coat/hair pigmentation	Bex2<tm1b(EUCOMM)Hmgu>/Bex2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bex2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756798	F	MP:0000218	increased leukocyte cell number	Bex2<tm1b(EUCOMM)Hmgu>/Bex2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bex2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756798	F	MP:0010068	decreased red blood cell distribution width	Bex2<tm1b(EUCOMM)Hmgu>/Bex2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bex2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756801	F	MP:0005553	increased circulating creatinine level	Blvrb<tm1(KOMP)Wtsi>/Blvrb<tm1(KOMP)Wtsi>	C57BL/6N-Blvrb<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5756803	M	MP:0001304	cataract	Bms1<tm1b(EUCOMM)Hmgu>/Bms1<+>	C57BL/6N-Bms1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756805	F	MP:0002968	increased circulating alkaline phosphatase level	Bnip2<tm1b(EUCOMM)Wtsi>/Bnip2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bnip2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756805	M	MP:0000559	abnormal femur morphology	Bnip2<tm1b(EUCOMM)Wtsi>/Bnip2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bnip2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756805	F	MP:0005561	increased mean corpuscular hemoglobin	Bnip2<tm1b(EUCOMM)Wtsi>/Bnip2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bnip2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756805	M	MP:0000558	abnormal tibia morphology	Bnip2<tm1b(EUCOMM)Wtsi>/Bnip2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bnip2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756805	F	MP:0010052	increased grip strength	Bnip2<tm1b(EUCOMM)Wtsi>/Bnip2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bnip2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756806	F	MP:0005419	decreased circulating serum albumin level	Boc<tm1b(KOMP)Wtsi>/Boc<tm1b(KOMP)Wtsi>	C57BL/6N-Boc<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756806	M	MP:0001488	increased startle reflex	Boc<tm1b(KOMP)Wtsi>/Boc<tm1b(KOMP)Wtsi>	C57BL/6N-Boc<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756806	F	MP:0001552	increased circulating triglyceride level	Boc<tm1b(KOMP)Wtsi>/Boc<tm1b(KOMP)Wtsi>	C57BL/6N-Boc<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756806	F	MP:0005567	decreased circulating total protein level	Boc<tm1b(KOMP)Wtsi>/Boc<tm1b(KOMP)Wtsi>	C57BL/6N-Boc<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756807	M	MP:0002606	increased basophil cell number	Bok<tm1b(EUCOMM)Hmgu>/Bok<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bok<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756807	F	MP:0005278	abnormal cholesterol homeostasis	Bok<tm1b(EUCOMM)Hmgu>/Bok<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bok<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756807	M	MP:0005011	increased eosinophil cell number	Bok<tm1b(EUCOMM)Hmgu>/Bok<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bok<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756808	F	MP:0020420	abnormal freezing behavior	Bphl<tm1b(EUCOMM)Hmgu>/Bphl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bphl<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5756809	M	MP:0000689	abnormal spleen morphology	Btbd16<tm2b(EUCOMM)Hmgu>/Btbd16<tm2b(EUCOMM)Hmgu>	C57BL/6N-Btbd16<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5756809	M	MP:0000691	enlarged spleen	Btbd16<tm2b(EUCOMM)Hmgu>/Btbd16<tm2b(EUCOMM)Hmgu>	C57BL/6N-Btbd16<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5756809	M	MP:0002644	decreased circulating triglyceride level	Btbd16<tm2b(EUCOMM)Hmgu>/Btbd16<tm2b(EUCOMM)Hmgu>	C57BL/6N-Btbd16<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5756809	M	MP:0004952	increased spleen weight	Btbd16<tm2b(EUCOMM)Hmgu>/Btbd16<tm2b(EUCOMM)Hmgu>	C57BL/6N-Btbd16<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5756810	F	MP:0010053	decreased grip strength	Btbd9<tm1b(EUCOMM)Wtsi>/Btbd9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Btbd9<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5756810	M	MP:0001556	increased circulating HDL cholesterol level	Btbd9<tm1b(EUCOMM)Wtsi>/Btbd9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Btbd9<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5756810	M	MP:0005178	increased circulating cholesterol level	Btbd9<tm1b(EUCOMM)Wtsi>/Btbd9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Btbd9<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5756810	M	MP:0013279	increased fasting circulating glucose level	Btbd9<tm1b(EUCOMM)Wtsi>/Btbd9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Btbd9<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5756811	M	MP:0002941	increased circulating alanine transaminase level	Btrc<tm1b(KOMP)Wtsi>/Btrc<tm1b(KOMP)Wtsi>	C57BL/6N-Btrc<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756811	M	MP:0000220	increased monocyte cell number	Btrc<tm1b(KOMP)Wtsi>/Btrc<tm1b(KOMP)Wtsi>	C57BL/6N-Btrc<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756814	M	MP:0001325	abnormal retina morphology	C1qtnf5<tm1.1(KOMP)Vlcg>/C1qtnf5<tm1.1(KOMP)Vlcg>	B6N(Cg)-C1qtnf5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756815	M	MP:0003961	decreased lean body mass	C1rl<tm1b(EUCOMM)Hmgu>/C1rl<tm1b(EUCOMM)Hmgu>	C57BL/6N-C1rl<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756815	F	MP:0002932	abnormal joint morphology	C1rl<tm1b(EUCOMM)Hmgu>/C1rl<tm1b(EUCOMM)Hmgu>	C57BL/6N-C1rl<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756815	F	MP:0000558	abnormal tibia morphology	C1rl<tm1b(EUCOMM)Hmgu>/C1rl<tm1b(EUCOMM)Hmgu>	C57BL/6N-C1rl<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756816	M	MP:0000274	enlarged heart	Cab39l<tm1b(EUCOMM)Wtsi>/Cab39l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cab39l<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756817	M	MP:0001510	abnormal coat appearance	Cabp1<tm1b(EUCOMM)Wtsi>/Cabp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cabp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756817	M	MP:0000220	increased monocyte cell number	Cabp1<tm1b(EUCOMM)Wtsi>/Cabp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cabp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756817	M	MP:0000219	increased neutrophil cell number	Cabp1<tm1b(EUCOMM)Wtsi>/Cabp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cabp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756817	M	MP:0010025	decreased total body fat amount	Cabp1<tm1b(EUCOMM)Wtsi>/Cabp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cabp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756817	M	MP:0005016	decreased lymphocyte cell number	Cabp1<tm1b(EUCOMM)Wtsi>/Cabp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cabp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756818	F	MP:0020870	decreased thigmotaxis	Cacna1b<tm1b(KOMP)Wtsi>/Cacna1b<tm1b(KOMP)Wtsi>	C57BL/6N-Cacna1b<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756818	F	MP:0001364	decreased anxiety-related response	Cacna1b<tm1b(KOMP)Wtsi>/Cacna1b<tm1b(KOMP)Wtsi>	C57BL/6N-Cacna1b<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756818	M	MP:0010053	decreased grip strength	Cacna1b<tm1b(KOMP)Wtsi>/Cacna1b<tm1b(KOMP)Wtsi>	C57BL/6N-Cacna1b<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756818	M	MP:0001415	increased exploration in new environment	Cacna1b<tm1b(KOMP)Wtsi>/Cacna1b<tm1b(KOMP)Wtsi>	C57BL/6N-Cacna1b<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756819	F	MP:0000601	small liver	Cacna1i<tm1b(KOMP)Wtsi>/Cacna1i<tm1b(KOMP)Wtsi>	C57BL/6N-Cacna1i<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756819	F	MP:0000689	abnormal spleen morphology	Cacna1i<tm1b(KOMP)Wtsi>/Cacna1i<tm1b(KOMP)Wtsi>	C57BL/6N-Cacna1i<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756819	F	MP:0002188	small heart	Cacna1i<tm1b(KOMP)Wtsi>/Cacna1i<tm1b(KOMP)Wtsi>	C57BL/6N-Cacna1i<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756819	M	MP:0001944	abnormal pancreas morphology	Cacna1i<tm1b(KOMP)Wtsi>/Cacna1i<tm1b(KOMP)Wtsi>	C57BL/6N-Cacna1i<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756819	F	MP:0002833	increased heart weight	Cacna1i<tm1b(KOMP)Wtsi>/Cacna1i<tm1b(KOMP)Wtsi>	C57BL/6N-Cacna1i<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756819	M	MP:0003019	increased circulating chloride level	Cacna1i<tm1b(KOMP)Wtsi>/Cacna1i<tm1b(KOMP)Wtsi>	C57BL/6N-Cacna1i<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756820	M	MP:0002599	increased mean platelet volume	Camkmt<tm1b(EUCOMM)Wtsi>/Camkmt<tm1b(EUCOMM)Wtsi>	C57BL/6N-Camkmt<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756820	M	MP:0010025	decreased total body fat amount	Camkmt<tm1b(EUCOMM)Wtsi>/Camkmt<tm1b(EUCOMM)Wtsi>	C57BL/6N-Camkmt<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756820	F	MP:0005633	increased circulating sodium level	Camkmt<tm1b(EUCOMM)Wtsi>/Camkmt<tm1b(EUCOMM)Wtsi>	C57BL/6N-Camkmt<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756820	M	MP:0005565	increased blood urea nitrogen level	Camkmt<tm1b(EUCOMM)Wtsi>/Camkmt<tm1b(EUCOMM)Wtsi>	C57BL/6N-Camkmt<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756821	M	MP:0011965	decreased total retina thickness	Cant1<tm1b(EUCOMM)Hmgu>/Cant1<+>	C57BL/6N-Cant1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756821	M	MP:0011886	increased circulating lipase level	Cant1<tm1b(EUCOMM)Hmgu>/Cant1<+>	C57BL/6N-Cant1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756821	F	MP:0001303	abnormal lens morphology	Cant1<tm1b(EUCOMM)Hmgu>/Cant1<+>	C57BL/6N-Cant1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756821	F	MP:0002699	abnormal vitreous body morphology	Cant1<tm1b(EUCOMM)Hmgu>/Cant1<+>	C57BL/6N-Cant1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756821	M	MP:0008806	increased circulating amylase level	Cant1<tm1b(EUCOMM)Hmgu>/Cant1<+>	C57BL/6N-Cant1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756821	F	MP:0002968	increased circulating alkaline phosphatase level	Cant1<tm1b(EUCOMM)Hmgu>/Cant1<+>	C57BL/6N-Cant1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756823	M	MP:0010067	increased red blood cell distribution width	Cap2<tm1b(EUCOMM)Wtsi>/Cap2<+>	C57BL/6N-Cap2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5756823	M	MP:0010570	prolonged ST segment	Cap2<tm1b(EUCOMM)Wtsi>/Cap2<+>	C57BL/6N-Cap2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5756823	M	MP:0005562	decreased mean corpuscular hemoglobin	Cap2<tm1b(EUCOMM)Wtsi>/Cap2<+>	C57BL/6N-Cap2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5756823	M	MP:0010506	prolonged RR interval	Cap2<tm1b(EUCOMM)Wtsi>/Cap2<+>	C57BL/6N-Cap2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5756823	M	MP:0003233	prolonged QT interval	Cap2<tm1b(EUCOMM)Wtsi>/Cap2<+>	C57BL/6N-Cap2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5756825	M	MP:0010053	decreased grip strength	Car4<tm1b(EUCOMM)Wtsi>/Car4<+>	C57BL/6N-Car4<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5756827	F	MP:0010570	prolonged ST segment	Carf<tm1.1(KOMP)Vlcg>/Carf<tm1.1(KOMP)Vlcg>	B6N(Cg)-Carf<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756831	M	MP:0001925	male infertility	Catip<tm1b(KOMP)Wtsi>/Catip<tm1b(KOMP)Wtsi>	C57BL/6N-Catip<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756831	M	MP:0002599	increased mean platelet volume	Catip<tm1b(KOMP)Wtsi>/Catip<tm1b(KOMP)Wtsi>	C57BL/6N-Catip<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756832	M	MP:0001289	persistence of hyaloid vascular system	Cbx2<tm1b(KOMP)Wtsi>/Cbx2<+>	C57BL/6N-Cbx2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756834	F	MP:0001399	hyperactivity	Cbx4<tm1.1(KOMP)Vlcg>/Cbx4<+>	C57BL/6N-Cbx4<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5756834	M	MP:0003961	decreased lean body mass	Cbx4<tm1.1(KOMP)Vlcg>/Cbx4<+>	C57BL/6N-Cbx4<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5756834	M	MP:0010024	increased total body fat amount	Cbx4<tm1.1(KOMP)Vlcg>/Cbx4<+>	C57BL/6N-Cbx4<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5756836	F	MP:0001523	impaired righting response	Mcub<tm1b(KOMP)Mbp>/Mcub<tm1b(KOMP)Mbp>	C57BL/6N-Mcub<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5756836	M	MP:0001284	absent vibrissae	Mcub<tm1b(KOMP)Mbp>/Mcub<tm1b(KOMP)Mbp>	C57BL/6N-Mcub<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5756837	F	MP:0000689	abnormal spleen morphology	Bicdl1<tm2b(EUCOMM)Wtsi>/Bicdl1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Bicdl1<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756837	F	MP:0000691	enlarged spleen	Bicdl1<tm2b(EUCOMM)Wtsi>/Bicdl1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Bicdl1<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756837	F	MP:0002757	decreased vertical activity	Bicdl1<tm2b(EUCOMM)Wtsi>/Bicdl1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Bicdl1<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756840	M	MP:0002135	abnormal kidney morphology	Cck<tm2b(EUCOMM)Hmgu>/Cck<tm2b(EUCOMM)Hmgu>	C57BL/6N-Cck<tm2b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5756841	M	MP:0005292	improved glucose tolerance	Ccl26<tm1.1(KOMP)Vlcg>/Ccl26<tm1.1(KOMP)Vlcg>	B6N(Cg)-Ccl26<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756841	F	MP:0011396	abnormal sleep behavior	Ccl26<tm1.1(KOMP)Vlcg>/Ccl26<tm1.1(KOMP)Vlcg>	B6N(Cg)-Ccl26<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756841	F	MP:0005561	increased mean corpuscular hemoglobin	Ccl26<tm1.1(KOMP)Vlcg>/Ccl26<tm1.1(KOMP)Vlcg>	B6N(Cg)-Ccl26<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756841	F	MP:0001399	hyperactivity	Ccl26<tm1.1(KOMP)Vlcg>/Ccl26<tm1.1(KOMP)Vlcg>	B6N(Cg)-Ccl26<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756843	F	MP:0005560	decreased circulating glucose level	Cd5l<tm1b(KOMP)Mbp>/Cd5l<tm1b(KOMP)Mbp>	C57BL/6N-Cd5l<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5756843	F	MP:0000062	increased bone mineral density	Cd5l<tm1b(KOMP)Mbp>/Cd5l<tm1b(KOMP)Mbp>	C57BL/6N-Cd5l<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5756843	M	MP:0000579	abnormal nail morphology	Cd5l<tm1b(KOMP)Mbp>/Cd5l<tm1b(KOMP)Mbp>	C57BL/6N-Cd5l<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5756844	M	MP:0001488	increased startle reflex	Cd84<tm1b(KOMP)Mbp>/Cd84<tm1b(KOMP)Mbp>	B6N(Cg)-Cd84<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5756845	M	MP:0002075	abnormal coat/hair pigmentation	Cdc123<tm1b(KOMP)Wtsi>/Cdc123<+>	C57BL/6N-Cdc123<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756845	M	MP:0001488	increased startle reflex	Cdc123<tm1b(KOMP)Wtsi>/Cdc123<+>	C57BL/6N-Cdc123<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756848	M	MP:0000579	abnormal nail morphology	Cdc34<tm1.1(KOMP)Mbp>/Cdc34<+>	B6N(Cg)-Cdc34<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5756849	M	MP:0001925	male infertility	Cdc34<tm1.1(KOMP)Mbp>/Cdc34<tm1.1(KOMP)Mbp>	B6N(Cg)-Cdc34<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5756850	M	MP:0003019	increased circulating chloride level	Cdca5<tm1.1(KOMP)Vlcg>/Cdca5<+>	B6N(Cg)-Cdca5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756850	M	MP:0002941	increased circulating alanine transaminase level	Cdca5<tm1.1(KOMP)Vlcg>/Cdca5<+>	B6N(Cg)-Cdca5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756850	M	MP:0005633	increased circulating sodium level	Cdca5<tm1.1(KOMP)Vlcg>/Cdca5<+>	B6N(Cg)-Cdca5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756852	M	MP:0002757	decreased vertical activity	Cdh4<tm1b(EUCOMM)Wtsi>/Cdh4<tm1b(EUCOMM)Wtsi>	B6N(Cg)-Cdh4<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5756852	F	MP:0005568	increased circulating total protein level	Cdh4<tm1b(EUCOMM)Wtsi>/Cdh4<tm1b(EUCOMM)Wtsi>	B6N(Cg)-Cdh4<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5756853	F	MP:0011972	decreased circulating lactate dehydrogenase level	Cdipt<tm1b(EUCOMM)Wtsi>/Cdipt<+>	C57BL/6N-Cdipt<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756853	M	MP:0003961	decreased lean body mass	Cdipt<tm1b(EUCOMM)Wtsi>/Cdipt<+>	C57BL/6N-Cdipt<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756853	M	MP:0010024	increased total body fat amount	Cdipt<tm1b(EUCOMM)Wtsi>/Cdipt<+>	C57BL/6N-Cdipt<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756856	F	MP:0001415	increased exploration in new environment	Cdkal1<tm2b(EUCOMM)Wtsi>/Cdkal1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Cdkal1<tm2b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5756858	M	MP:0011886	increased circulating lipase level	Cenpe<tm1b(EUCOMM)Hmgu>/Cenpe<+>	C57BL/6N-Cenpe<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5756858	M	MP:0013279	increased fasting circulating glucose level	Cenpe<tm1b(EUCOMM)Hmgu>/Cenpe<+>	C57BL/6N-Cenpe<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5756860	M	MP:0000186	decreased circulating HDL cholesterol level	Cenph<tm1b(EUCOMM)Hmgu>/Cenph<+>	C57BL/6N-Cenph<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756863	M	MP:0002608	increased hematocrit	Cfb<tm1.1(KOMP)Wtsi>/Cfb<tm1.1(KOMP)Wtsi>	C57BL/6N-Cfb<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756863	M	MP:0000198	decreased circulating phosphate level	Cfb<tm1.1(KOMP)Wtsi>/Cfb<tm1.1(KOMP)Wtsi>	C57BL/6N-Cfb<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756863	M	MP:0003131	increased erythrocyte cell number	Cfb<tm1.1(KOMP)Wtsi>/Cfb<tm1.1(KOMP)Wtsi>	C57BL/6N-Cfb<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756863	F	MP:0013279	increased fasting circulating glucose level	Cfb<tm1.1(KOMP)Wtsi>/Cfb<tm1.1(KOMP)Wtsi>	C57BL/6N-Cfb<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756863	M	MP:0005564	increased hemoglobin content	Cfb<tm1.1(KOMP)Wtsi>/Cfb<tm1.1(KOMP)Wtsi>	C57BL/6N-Cfb<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756864	F	MP:0001402	decreased locomotor activity	Cfi<tm1b(EUCOMM)Hmgu>/Cfi<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cfi<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756864	M	MP:0003179	thrombocytopenia	Cfi<tm1b(EUCOMM)Hmgu>/Cfi<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cfi<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756865	M	MP:0010052	increased grip strength	Chd1<tm1b(KOMP)Wtsi>/Chd1<+>	C57BL/6N-Chd1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756865	M	MP:0001293	anophthalmia	Chd1<tm1b(KOMP)Wtsi>/Chd1<+>	C57BL/6N-Chd1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756865	M	MP:0000455	abnormal maxilla morphology	Chd1<tm1b(KOMP)Wtsi>/Chd1<+>	C57BL/6N-Chd1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756865	M	MP:0002100	abnormal tooth morphology	Chd1<tm1b(KOMP)Wtsi>/Chd1<+>	C57BL/6N-Chd1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756867	F	MP:0009142	decreased prepulse inhibition	Chd2<tm1b(EUCOMM)Hmgu>/Chd2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chd2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756867	M	MP:0002874	decreased hemoglobin content	Chd2<tm1b(EUCOMM)Hmgu>/Chd2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chd2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756867	F	MP:0001258	decreased body length	Chd2<tm1b(EUCOMM)Hmgu>/Chd2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chd2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756867	M	MP:0002941	increased circulating alanine transaminase level	Chd2<tm1b(EUCOMM)Hmgu>/Chd2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chd2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756867	F	MP:0003795	abnormal bone structure	Chd2<tm1b(EUCOMM)Hmgu>/Chd2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chd2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756867	M	MP:0002875	decreased erythrocyte cell number	Chd2<tm1b(EUCOMM)Hmgu>/Chd2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chd2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756867	F	MP:0010124	decreased bone mineral content	Chd2<tm1b(EUCOMM)Hmgu>/Chd2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chd2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756867	F	MP:0000063	decreased bone mineral density	Chd2<tm1b(EUCOMM)Hmgu>/Chd2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chd2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756867	F	MP:0004122	abnormal sinus arrhythmia	Chd2<tm1b(EUCOMM)Hmgu>/Chd2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chd2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756867	M	MP:0005343	increased circulating aspartate transaminase level	Chd2<tm1b(EUCOMM)Hmgu>/Chd2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chd2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756869	M	MP:0005633	increased circulating sodium level	Chek2<tm1b(EUCOMM)Hmgu>/Chek2<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Chek2<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5756870	F	MP:0002075	abnormal coat/hair pigmentation	Chic2<tm1b(EUCOMM)Wtsi>/Chic2<+>	C57BL/6N-Chic2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756870	F	MP:0004832	enlarged ovary	Chic2<tm1b(EUCOMM)Wtsi>/Chic2<+>	C57BL/6N-Chic2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756870	F	MP:0000274	enlarged heart	Chic2<tm1b(EUCOMM)Wtsi>/Chic2<+>	C57BL/6N-Chic2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756870	F	MP:0000691	enlarged spleen	Chic2<tm1b(EUCOMM)Wtsi>/Chic2<+>	C57BL/6N-Chic2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756870	F	MP:0008806	increased circulating amylase level	Chic2<tm1b(EUCOMM)Wtsi>/Chic2<+>	C57BL/6N-Chic2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756870	M	MP:0004222	iris synechia	Chic2<tm1b(EUCOMM)Wtsi>/Chic2<+>	C57BL/6N-Chic2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756873	M	MP:0001417	decreased exploration in new environment	Chp2<tm1b(KOMP)Mbp>/Chp2<+>	B6N(Cg)-Chp2<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5756873	M	MP:0013278	decreased fasting circulating glucose level	Chp2<tm1b(KOMP)Mbp>/Chp2<+>	B6N(Cg)-Chp2<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5756873	M	MP:0010052	increased grip strength	Chp2<tm1b(KOMP)Mbp>/Chp2<+>	B6N(Cg)-Chp2<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5756875	F	MP:0005178	increased circulating cholesterol level	Chrna7<tm1b(EUCOMM)Hmgu>/Chrna7<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chrna7<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756875	F	MP:0001556	increased circulating HDL cholesterol level	Chrna7<tm1b(EUCOMM)Hmgu>/Chrna7<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chrna7<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756876	M	MP:0002631	abnormal epididymis morphology	Chrnb2<tm1b(EUCOMM)Hmgu>/Chrnb2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chrnb2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756876	M	MP:0010024	increased total body fat amount	Chrnb2<tm1b(EUCOMM)Hmgu>/Chrnb2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chrnb2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756876	M	MP:0000274	enlarged heart	Chrnb2<tm1b(EUCOMM)Hmgu>/Chrnb2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chrnb2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756877	F	MP:0001513	limb grasping	Cib2<tm1b(EUCOMM)Wtsi>/Cib2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cib2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756877	F	MP:0010087	increased circulating fructosamine level	Cib2<tm1b(EUCOMM)Wtsi>/Cib2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cib2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756877	M	MP:0002606	increased basophil cell number	Cib2<tm1b(EUCOMM)Wtsi>/Cib2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cib2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756877	F	MP:0001556	increased circulating HDL cholesterol level	Cib2<tm1b(EUCOMM)Wtsi>/Cib2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cib2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756877	M	MP:0001552	increased circulating triglyceride level	Cib2<tm1b(EUCOMM)Wtsi>/Cib2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cib2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756877	M	MP:0000745	tremors	Cib2<tm1b(EUCOMM)Wtsi>/Cib2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cib2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756877	M	MP:0001489	decreased startle reflex	Cib2<tm1b(EUCOMM)Wtsi>/Cib2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cib2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756879	M	MP:0003019	increased circulating chloride level	Clk1<tm1a(EUCOMM)Wtsi>/Clk1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clk1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5756879	M	MP:0000745	tremors	Clk1<tm1a(EUCOMM)Wtsi>/Clk1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clk1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5756879	F	MP:0001325	abnormal retina morphology	Clk1<tm1a(EUCOMM)Wtsi>/Clk1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Clk1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5756881	M	MP:0010025	decreased total body fat amount	Cln6<tm1b(EUCOMM)Hmgu>/Cln6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cln6<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756881	F	MP:0009142	decreased prepulse inhibition	Cln6<tm1b(EUCOMM)Hmgu>/Cln6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cln6<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756881	F	MP:0002833	increased heart weight	Cln6<tm1b(EUCOMM)Hmgu>/Cln6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cln6<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756883	F	MP:0010124	decreased bone mineral content	Clstn1<tm1b(EUCOMM)Hmgu>/Clstn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Clstn1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756883	F	MP:0002590	increased mean corpuscular volume	Clstn1<tm1b(EUCOMM)Hmgu>/Clstn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Clstn1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756883	M	MP:0001289	persistence of hyaloid vascular system	Clstn1<tm1b(EUCOMM)Hmgu>/Clstn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Clstn1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756884	F	MP:0003917	increased kidney weight	Clstn3<tm1b(EUCOMM)Hmgu>/Clstn3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Clstn3<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5756884	M	MP:0004953	decreased spleen weight	Clstn3<tm1b(EUCOMM)Hmgu>/Clstn3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Clstn3<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5756884	M	MP:0000745	tremors	Clstn3<tm1b(EUCOMM)Hmgu>/Clstn3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Clstn3<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5756884	M	MP:0001406	abnormal gait	Clstn3<tm1b(EUCOMM)Hmgu>/Clstn3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Clstn3<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5756884	M	MP:0001175	abnormal lung morphology	Clstn3<tm1b(EUCOMM)Hmgu>/Clstn3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Clstn3<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5756885	F	MP:0005655	increased aggression	Clu<tm1b(EUCOMM)Hmgu>/Clu<tm1b(EUCOMM)Hmgu>	C57BL/6N-Clu<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756886	F	MP:0013278	decreased fasting circulating glucose level	Clvs1<tm1.1(KOMP)Vlcg>/Clvs1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Clvs1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756886	F	MP:0003064	decreased coping response	Clvs1<tm1.1(KOMP)Vlcg>/Clvs1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Clvs1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756886	F	MP:0000063	decreased bone mineral density	Clvs1<tm1.1(KOMP)Vlcg>/Clvs1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Clvs1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756886	F	MP:0003019	increased circulating chloride level	Clvs1<tm1.1(KOMP)Vlcg>/Clvs1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Clvs1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756886	F	MP:0009142	decreased prepulse inhibition	Clvs1<tm1.1(KOMP)Vlcg>/Clvs1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Clvs1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756890	M	MP:0002768	small adrenal glands	Coa5<tm1b(KOMP)Wtsi>/Coa5<+>	C57BL/6N-Coa5<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756890	M	MP:0001402	decreased locomotor activity	Coa5<tm1b(KOMP)Wtsi>/Coa5<+>	C57BL/6N-Coa5<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756890	F	MP:0001120	abnormal uterus morphology	Coa5<tm1b(KOMP)Wtsi>/Coa5<+>	C57BL/6N-Coa5<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756892	M	MP:0002079	increased circulating insulin level	Cog3<tm1b(EUCOMM)Hmgu>/Cog3<+>	C57BL/6N-Cog3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756894	M	MP:0005293	impaired glucose tolerance	Col14a1<tm1b(KOMP)Wtsi>/Col14a1<tm1b(KOMP)Wtsi>	C57BL/6N-Col14a1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756895	M	MP:0000558	abnormal tibia morphology	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756895	M	MP:0000559	abnormal femur morphology	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756895	F	MP:0002968	increased circulating alkaline phosphatase level	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756895	M	MP:0010025	decreased total body fat amount	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756895	F	MP:0005566	decreased blood urea nitrogen level	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756895	M	MP:0000062	increased bone mineral density	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756895	M	MP:0002833	increased heart weight	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756895	M	MP:0010123	increased bone mineral content	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756895	M	MP:0002753	dilated heart left ventricle	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756896	F	MP:0001258	decreased body length	Col24a1<tm1b(EUCOMM)Wtsi>/Col24a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col24a1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756897	F	MP:0001319	irregularly shaped pupil	Col4a3<tm1b(EUCOMM)Wtsi>/Col4a3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756897	M	MP:0012362	increased large unstained cell number	Col4a3<tm1b(EUCOMM)Wtsi>/Col4a3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756897	M	MP:0005016	decreased lymphocyte cell number	Col4a3<tm1b(EUCOMM)Wtsi>/Col4a3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756897	M	MP:0003917	increased kidney weight	Col4a3<tm1b(EUCOMM)Wtsi>/Col4a3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756897	M	MP:0002874	decreased hemoglobin content	Col4a3<tm1b(EUCOMM)Wtsi>/Col4a3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756897	F	MP:0002607	decreased basophil cell number	Col4a3<tm1b(EUCOMM)Wtsi>/Col4a3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756897	M	MP:0000219	increased neutrophil cell number	Col4a3<tm1b(EUCOMM)Wtsi>/Col4a3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756898	M	MP:0000218	increased leukocyte cell number	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0005178	increased circulating cholesterol level	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0001303	abnormal lens morphology	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0005505	thrombocytosis	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0002135	abnormal kidney morphology	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0005562	decreased mean corpuscular hemoglobin	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0008806	increased circulating amylase level	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0000208	decreased hematocrit	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0000194	increased circulating calcium level	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0005419	decreased circulating serum albumin level	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0002875	decreased erythrocyte cell number	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0001289	persistence of hyaloid vascular system	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0005565	increased blood urea nitrogen level	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0005553	increased circulating creatinine level	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0005567	decreased circulating total protein level	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0001552	increased circulating triglyceride level	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0002874	decreased hemoglobin content	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0002591	decreased mean corpuscular volume	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756898	M	MP:0010088	decreased circulating fructosamine level	Col4a5<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0005567	decreased circulating total protein level	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0000194	increased circulating calcium level	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0010025	decreased total body fat amount	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0002874	decreased hemoglobin content	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0008806	increased circulating amylase level	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0000208	decreased hematocrit	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0010067	increased red blood cell distribution width	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0012362	increased large unstained cell number	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0004952	increased spleen weight	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0005419	decreased circulating serum albumin level	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0005553	increased circulating creatinine level	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0001566	increased circulating phosphate level	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0005505	thrombocytosis	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0001552	increased circulating triglyceride level	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0001556	increased circulating HDL cholesterol level	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0005565	increased blood urea nitrogen level	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0000219	increased neutrophil cell number	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0005293	impaired glucose tolerance	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0002135	abnormal kidney morphology	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0010088	decreased circulating fructosamine level	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0005178	increased circulating cholesterol level	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756899	F	MP:0002875	decreased erythrocyte cell number	Col4a5<tm1b(EUCOMM)Wtsi>/Col4a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col4a5<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756900	M	MP:0001402	decreased locomotor activity	Col9a2<tm1b(EUCOMM)Wtsi>/Col9a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col9a2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756900	M	MP:0009142	decreased prepulse inhibition	Col9a2<tm1b(EUCOMM)Wtsi>/Col9a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col9a2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756900	M	MP:0000552	abnormal radius morphology	Col9a2<tm1b(EUCOMM)Wtsi>/Col9a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col9a2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756900	F	MP:0002102	abnormal ear morphology	Col9a2<tm1b(EUCOMM)Wtsi>/Col9a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col9a2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756900	F	MP:0001552	increased circulating triglyceride level	Col9a2<tm1b(EUCOMM)Wtsi>/Col9a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col9a2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756900	F	MP:0004509	abnormal pelvic girdle bone morphology	Col9a2<tm1b(EUCOMM)Wtsi>/Col9a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col9a2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756900	F	MP:0002968	increased circulating alkaline phosphatase level	Col9a2<tm1b(EUCOMM)Wtsi>/Col9a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col9a2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756901	M	MP:0010088	decreased circulating fructosamine level	Commd9<tm1b(KOMP)Wtsi>/Commd9<+>	C57BL/6N-Commd9<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756901	M	MP:0002875	decreased erythrocyte cell number	Commd9<tm1b(KOMP)Wtsi>/Commd9<+>	C57BL/6N-Commd9<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756901	M	MP:0002874	decreased hemoglobin content	Commd9<tm1b(KOMP)Wtsi>/Commd9<+>	C57BL/6N-Commd9<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756901	M	MP:0005016	decreased lymphocyte cell number	Commd9<tm1b(KOMP)Wtsi>/Commd9<+>	C57BL/6N-Commd9<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756901	M	MP:0005419	decreased circulating serum albumin level	Commd9<tm1b(KOMP)Wtsi>/Commd9<+>	C57BL/6N-Commd9<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756901	M	MP:0001402	decreased locomotor activity	Commd9<tm1b(KOMP)Wtsi>/Commd9<+>	C57BL/6N-Commd9<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756901	M	MP:0010067	increased red blood cell distribution width	Commd9<tm1b(KOMP)Wtsi>/Commd9<+>	C57BL/6N-Commd9<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756901	M	MP:0000219	increased neutrophil cell number	Commd9<tm1b(KOMP)Wtsi>/Commd9<+>	C57BL/6N-Commd9<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756903	F	MP:0001399	hyperactivity	Comt<tm1b(EUCOMM)Wtsi>/Comt<tm1b(EUCOMM)Wtsi>	C57BL/6N-Comt<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756903	F	MP:0004924	abnormal behavior	Comt<tm1b(EUCOMM)Wtsi>/Comt<tm1b(EUCOMM)Wtsi>	C57BL/6N-Comt<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756903	F	MP:0010052	increased grip strength	Comt<tm1b(EUCOMM)Wtsi>/Comt<tm1b(EUCOMM)Wtsi>	C57BL/6N-Comt<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756903	F	MP:0001392	abnormal locomotor behavior	Comt<tm1b(EUCOMM)Wtsi>/Comt<tm1b(EUCOMM)Wtsi>	C57BL/6N-Comt<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756903	F	MP:0001364	decreased anxiety-related response	Comt<tm1b(EUCOMM)Wtsi>/Comt<tm1b(EUCOMM)Wtsi>	C57BL/6N-Comt<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756903	M	MP:0005419	decreased circulating serum albumin level	Comt<tm1b(EUCOMM)Wtsi>/Comt<tm1b(EUCOMM)Wtsi>	C57BL/6N-Comt<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756903	F	MP:0020870	decreased thigmotaxis	Comt<tm1b(EUCOMM)Wtsi>/Comt<tm1b(EUCOMM)Wtsi>	C57BL/6N-Comt<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756904	M	MP:0003961	decreased lean body mass	Coq2<tm1b(EUCOMM)Hmgu>/Coq2<+>	C57BL/6N-Coq2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756906	F	MP:0001697	abnormal embryo size	Coq6<tm1b(EUCOMM)Hmgu>/Coq6<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Coq6<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5756907	M	MP:0001566	increased circulating phosphate level	Cox19<tm1b(EUCOMM)Hmgu>/Cox19<+>	C57BL/6N-Cox19<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756907	M	MP:0000702	enlarged lymph nodes	Cox19<tm1b(EUCOMM)Hmgu>/Cox19<+>	C57BL/6N-Cox19<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756909	F	MP:0001415	increased exploration in new environment	Cox4i1<tm1.1(KOMP)Vlcg>/Cox4i1<+>	C57BL/6N-Cox4i1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5756912	F	MP:0003020	decreased circulating chloride level	Cpa2<tm1b(EUCOMM)Hmgu>/Cpa2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpa2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756912	F	MP:0001926	female infertility	Cpa2<tm1b(EUCOMM)Hmgu>/Cpa2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpa2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756913	M	MP:0005560	decreased circulating glucose level	Cpb1<tm1.1(KOMP)Vlcg>/Cpb1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cpb1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756914	F	MP:0005343	increased circulating aspartate transaminase level	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	M	MP:0001925	male infertility	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	F	MP:0002941	increased circulating alanine transaminase level	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	F	MP:0000194	increased circulating calcium level	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	M	MP:0001258	decreased body length	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	F	MP:0003020	decreased circulating chloride level	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	F	MP:0002590	increased mean corpuscular volume	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	F	MP:0000218	increased leukocyte cell number	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	F	MP:0002968	increased circulating alkaline phosphatase level	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	M	MP:0001392	abnormal locomotor behavior	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	F	MP:0002608	increased hematocrit	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	M	MP:0001488	increased startle reflex	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	F	MP:0010463	aorta stenosis	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756914	F	MP:0005559	increased circulating glucose level	Cpe<tm1b(EUCOMM)Hmgu>/Cpe<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cpe<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756916	M	MP:0001566	increased circulating phosphate level	Cpt2<tm1b(KOMP)Wtsi>/Cpt2<+>	C57BL/6N-Cpt2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756916	M	MP:0000137	abnormal vertebrae morphology	Cpt2<tm1b(KOMP)Wtsi>/Cpt2<+>	C57BL/6N-Cpt2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756918	M	MP:0001925	male infertility	Creld2<tm1b(EUCOMM)Hmgu>/Creld2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Creld2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756918	F	MP:0002953	thick ventricular wall	Creld2<tm1b(EUCOMM)Hmgu>/Creld2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Creld2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756920	M	MP:0002591	decreased mean corpuscular volume	Crlf3<tm1b(KOMP)Wtsi>/Crlf3<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Crlf3<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756922	M	MP:0004952	increased spleen weight	Ctdspl2<tm2b(KOMP)Wtsi>/Ctdspl2<+>	C57BL/6N-Ctdspl2<tm2b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756922	M	MP:0010025	decreased total body fat amount	Ctdspl2<tm2b(KOMP)Wtsi>/Ctdspl2<+>	C57BL/6N-Ctdspl2<tm2b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756922	M	MP:0003960	increased lean body mass	Ctdspl2<tm2b(KOMP)Wtsi>/Ctdspl2<+>	C57BL/6N-Ctdspl2<tm2b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756924	M	MP:0005343	increased circulating aspartate transaminase level	Ctdspl<tm1.1(KOMP)Mbp>/Ctdspl<tm1.1(KOMP)Mbp>	C57BL/6N-Ctdspl<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5756924	F	MP:0005419	decreased circulating serum albumin level	Ctdspl<tm1.1(KOMP)Mbp>/Ctdspl<tm1.1(KOMP)Mbp>	C57BL/6N-Ctdspl<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5756924	M	MP:0005293	impaired glucose tolerance	Ctdspl<tm1.1(KOMP)Mbp>/Ctdspl<tm1.1(KOMP)Mbp>	C57BL/6N-Ctdspl<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5756924	F	MP:0005567	decreased circulating total protein level	Ctdspl<tm1.1(KOMP)Mbp>/Ctdspl<tm1.1(KOMP)Mbp>	C57BL/6N-Ctdspl<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5756928	M	MP:0000745	tremors	Cts6<tm1b(KOMP)Wtsi>/Cts6<tm1b(KOMP)Wtsi>	C57BL/6N-Cts6<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5756929	F	MP:0001314	cornea opacity	Ctsd<tm1b(EUCOMM)Wtsi>/Ctsd<+>	C57BL/6N-Ctsd<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5756929	F	MP:0005343	increased circulating aspartate transaminase level	Ctsd<tm1b(EUCOMM)Wtsi>/Ctsd<+>	C57BL/6N-Ctsd<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5756929	F	MP:0000208	decreased hematocrit	Ctsd<tm1b(EUCOMM)Wtsi>/Ctsd<+>	C57BL/6N-Ctsd<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5756931	F	MP:0009142	decreased prepulse inhibition	Ctsk<tm1b(EUCOMM)Hmgu>/Ctsk<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ctsk<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756931	F	MP:0001120	abnormal uterus morphology	Ctsk<tm1b(EUCOMM)Hmgu>/Ctsk<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ctsk<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756932	F	MP:0005635	decreased circulating bilirubin level	Ctso<tm2b(KOMP)Wtsi>/Ctso<tm2b(KOMP)Wtsi>	C57BL/6N-Ctso<tm2b(KOMP)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756932	F	MP:0002599	increased mean platelet volume	Ctso<tm2b(KOMP)Wtsi>/Ctso<tm2b(KOMP)Wtsi>	C57BL/6N-Ctso<tm2b(KOMP)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756932	M	MP:0002098	abnormal vibrissa morphology	Ctso<tm2b(KOMP)Wtsi>/Ctso<tm2b(KOMP)Wtsi>	C57BL/6N-Ctso<tm2b(KOMP)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756932	F	MP:0000195	decreased circulating calcium level	Ctso<tm2b(KOMP)Wtsi>/Ctso<tm2b(KOMP)Wtsi>	C57BL/6N-Ctso<tm2b(KOMP)Wtsi>/Cnrm	N	MGI:5576271
MGI:5756933	M	MP:0020870	decreased thigmotaxis	Cttn<tm1b(EUCOMM)Hmgu>/Cttn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cttn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756933	F	MP:0000745	tremors	Cttn<tm1b(EUCOMM)Hmgu>/Cttn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cttn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756934	M	MP:0005013	increased lymphocyte cell number	Cxcl9<tm1b(EUCOMM)Wtsi>/Cxcl9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl9<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756934	M	MP:0005178	increased circulating cholesterol level	Cxcl9<tm1b(EUCOMM)Wtsi>/Cxcl9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl9<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756934	M	MP:0013278	decreased fasting circulating glucose level	Cxcl9<tm1b(EUCOMM)Wtsi>/Cxcl9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl9<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756934	M	MP:0001556	increased circulating HDL cholesterol level	Cxcl9<tm1b(EUCOMM)Wtsi>/Cxcl9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl9<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756934	M	MP:0000222	decreased neutrophil cell number	Cxcl9<tm1b(EUCOMM)Wtsi>/Cxcl9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cxcl9<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	F	MP:0003795	abnormal bone structure	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	F	MP:0001552	increased circulating triglyceride level	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	F	MP:0008806	increased circulating amylase level	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	F	MP:0002968	increased circulating alkaline phosphatase level	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	F	MP:0001417	decreased exploration in new environment	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	M	MP:0000274	enlarged heart	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	M	MP:0010097	abnormal retina blood vessel morphology	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	F	MP:0005343	increased circulating aspartate transaminase level	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	M	MP:0001406	abnormal gait	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	M	MP:0005560	decreased circulating glucose level	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	M	MP:0005287	narrow eye opening	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	M	MP:0005567	decreased circulating total protein level	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	M	MP:0001322	abnormal iris morphology	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756935	F	MP:0000443	abnormal snout morphology	Cyb561<tm1b(EUCOMM)Wtsi>/Cyb561<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756937	F	MP:0004952	increased spleen weight	Cybb<tm2b(KOMP)Wtsi>/Cybb<tm2b(KOMP)Wtsi>	C57BL/6N-Cybb<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756937	F	MP:0002591	decreased mean corpuscular volume	Cybb<tm2b(KOMP)Wtsi>/Cybb<tm2b(KOMP)Wtsi>	C57BL/6N-Cybb<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756939	F	MP:0000198	decreased circulating phosphate level	Cyp17a1<tm1b(EUCOMM)Wtsi>/Cyp17a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp17a1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756939	F	MP:0002834	decreased heart weight	Cyp17a1<tm1b(EUCOMM)Wtsi>/Cyp17a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp17a1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756939	F	MP:0001402	decreased locomotor activity	Cyp17a1<tm1b(EUCOMM)Wtsi>/Cyp17a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp17a1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756939	M	MP:0005292	improved glucose tolerance	Cyp17a1<tm1b(EUCOMM)Wtsi>/Cyp17a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp17a1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756939	F	MP:0010053	decreased grip strength	Cyp17a1<tm1b(EUCOMM)Wtsi>/Cyp17a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp17a1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756939	F	MP:0003795	abnormal bone structure	Cyp17a1<tm1b(EUCOMM)Wtsi>/Cyp17a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp17a1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756939	M	MP:0001529	abnormal vocalization	Cyp17a1<tm1b(EUCOMM)Wtsi>/Cyp17a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp17a1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756939	M	MP:0002968	increased circulating alkaline phosphatase level	Cyp17a1<tm1b(EUCOMM)Wtsi>/Cyp17a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp17a1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756939	M	MP:0005553	increased circulating creatinine level	Cyp17a1<tm1b(EUCOMM)Wtsi>/Cyp17a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp17a1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756939	F	MP:0005565	increased blood urea nitrogen level	Cyp17a1<tm1b(EUCOMM)Wtsi>/Cyp17a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp17a1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756940	F	MP:0003795	abnormal bone structure	Cyp27b1<tm1b(EUCOMM)Hmgu>/Cyp27b1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp27b1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756940	M	MP:0010025	decreased total body fat amount	Cyp27b1<tm1b(EUCOMM)Hmgu>/Cyp27b1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp27b1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756940	M	MP:0005016	decreased lymphocyte cell number	Cyp27b1<tm1b(EUCOMM)Hmgu>/Cyp27b1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp27b1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756940	F	MP:0001417	decreased exploration in new environment	Cyp27b1<tm1b(EUCOMM)Hmgu>/Cyp27b1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp27b1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756940	F	MP:0000198	decreased circulating phosphate level	Cyp27b1<tm1b(EUCOMM)Hmgu>/Cyp27b1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp27b1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756940	M	MP:0000221	decreased leukocyte cell number	Cyp27b1<tm1b(EUCOMM)Hmgu>/Cyp27b1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp27b1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756940	M	MP:0005344	increased circulating bilirubin level	Cyp27b1<tm1b(EUCOMM)Hmgu>/Cyp27b1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp27b1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5756941	F	MP:0011954	shortened PQ interval	Cyp4b1<tm1b(KOMP)Wtsi>/Cyp4b1<tm1b(KOMP)Wtsi>	C57BL/6N-Cyp4b1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756941	M	MP:0005566	decreased blood urea nitrogen level	Cyp4b1<tm1b(KOMP)Wtsi>/Cyp4b1<tm1b(KOMP)Wtsi>	C57BL/6N-Cyp4b1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756941	F	MP:0005344	increased circulating bilirubin level	Cyp4b1<tm1b(KOMP)Wtsi>/Cyp4b1<tm1b(KOMP)Wtsi>	C57BL/6N-Cyp4b1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756941	M	MP:0002644	decreased circulating triglyceride level	Cyp4b1<tm1b(KOMP)Wtsi>/Cyp4b1<tm1b(KOMP)Wtsi>	C57BL/6N-Cyp4b1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756941	F	MP:0001415	increased exploration in new environment	Cyp4b1<tm1b(KOMP)Wtsi>/Cyp4b1<tm1b(KOMP)Wtsi>	C57BL/6N-Cyp4b1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756941	M	MP:0013279	increased fasting circulating glucose level	Cyp4b1<tm1b(KOMP)Wtsi>/Cyp4b1<tm1b(KOMP)Wtsi>	C57BL/6N-Cyp4b1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756941	F	MP:0010511	shortened PR interval	Cyp4b1<tm1b(KOMP)Wtsi>/Cyp4b1<tm1b(KOMP)Wtsi>	C57BL/6N-Cyp4b1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756941	M	MP:0005343	increased circulating aspartate transaminase level	Cyp4b1<tm1b(KOMP)Wtsi>/Cyp4b1<tm1b(KOMP)Wtsi>	C57BL/6N-Cyp4b1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756943	F	MP:0005293	impaired glucose tolerance	Cyp7b1<tm1b(EUCOMM)Wtsi>/Cyp7b1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp7b1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756943	M	MP:0011965	decreased total retina thickness	Cyp7b1<tm1b(EUCOMM)Wtsi>/Cyp7b1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp7b1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756944	M	MP:0002757	decreased vertical activity	Cystm1<tm1b(EUCOMM)Hmgu>/Cystm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cystm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756944	M	MP:0001417	decreased exploration in new environment	Cystm1<tm1b(EUCOMM)Hmgu>/Cystm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cystm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756944	F	MP:0002968	increased circulating alkaline phosphatase level	Cystm1<tm1b(EUCOMM)Hmgu>/Cystm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cystm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756944	F	MP:0010379	decreased respiratory quotient	Cystm1<tm1b(EUCOMM)Hmgu>/Cystm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cystm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756944	F	MP:0004924	abnormal behavior	Cystm1<tm1b(EUCOMM)Hmgu>/Cystm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cystm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756944	F	MP:0003961	decreased lean body mass	Cystm1<tm1b(EUCOMM)Hmgu>/Cystm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cystm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756944	F	MP:0020870	decreased thigmotaxis	Cystm1<tm1b(EUCOMM)Hmgu>/Cystm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cystm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756944	F	MP:0010024	increased total body fat amount	Cystm1<tm1b(EUCOMM)Hmgu>/Cystm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cystm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756944	F	MP:0001364	decreased anxiety-related response	Cystm1<tm1b(EUCOMM)Hmgu>/Cystm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cystm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756944	F	MP:0011940	decreased food intake	Cystm1<tm1b(EUCOMM)Hmgu>/Cystm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cystm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756945	M	MP:0013278	decreased fasting circulating glucose level	Macir<tm1.1(KOMP)Vlcg>/Macir<+>	B6N(Cg)-Macir<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756945	M	MP:0005633	increased circulating sodium level	Macir<tm1.1(KOMP)Vlcg>/Macir<+>	B6N(Cg)-Macir<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756945	F	MP:0003019	increased circulating chloride level	Macir<tm1.1(KOMP)Vlcg>/Macir<+>	B6N(Cg)-Macir<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756947	M	MP:0001147	small testis	D1Pas1<tm1(KOMP)Vlcg>/D1Pas1<tm1(KOMP)Vlcg>	C57BL/6N-D1Pas1<tm1(KOMP)Vlcg>/D4Rbrc	N	MGI:5576271
MGI:5756947	M	MP:0001925	male infertility	D1Pas1<tm1(KOMP)Vlcg>/D1Pas1<tm1(KOMP)Vlcg>	C57BL/6N-D1Pas1<tm1(KOMP)Vlcg>/D4Rbrc	N	MGI:5576271
MGI:5756948	M	MP:0001325	abnormal retina morphology	D630023F18Rik<tm1b(KOMP)Wtsi>/D630023F18Rik<tm1b(KOMP)Wtsi>	C57BL/6N-D630023F18Rik<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756949	F	MP:0010053	decreased grip strength	D630045J12Rik<tm1b(KOMP)Wtsi>/D630045J12Rik<tm1b(KOMP)Wtsi>	C57BL/6N-D630045J12Rik<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756949	M	MP:0000702	enlarged lymph nodes	D630045J12Rik<tm1b(KOMP)Wtsi>/D630045J12Rik<tm1b(KOMP)Wtsi>	C57BL/6N-D630045J12Rik<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756949	M	MP:0013279	increased fasting circulating glucose level	D630045J12Rik<tm1b(KOMP)Wtsi>/D630045J12Rik<tm1b(KOMP)Wtsi>	C57BL/6N-D630045J12Rik<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756949	M	MP:0010025	decreased total body fat amount	D630045J12Rik<tm1b(KOMP)Wtsi>/D630045J12Rik<tm1b(KOMP)Wtsi>	C57BL/6N-D630045J12Rik<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756949	M	MP:0002644	decreased circulating triglyceride level	D630045J12Rik<tm1b(KOMP)Wtsi>/D630045J12Rik<tm1b(KOMP)Wtsi>	C57BL/6N-D630045J12Rik<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756949	M	MP:0001417	decreased exploration in new environment	D630045J12Rik<tm1b(KOMP)Wtsi>/D630045J12Rik<tm1b(KOMP)Wtsi>	C57BL/6N-D630045J12Rik<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5756950	F	MP:0008806	increased circulating amylase level	Daam1<tm1b(EUCOMM)Hmgu>/Daam1<+>	C57BL/6N-Daam1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756952	M	MP:0000455	abnormal maxilla morphology	Daam2<tm1b(KOMP)Wtsi>/Daam2<tm1b(KOMP)Wtsi>	C57BL/6N-Daam2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756952	F	MP:0012362	increased large unstained cell number	Daam2<tm1b(KOMP)Wtsi>/Daam2<tm1b(KOMP)Wtsi>	C57BL/6N-Daam2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756952	F	MP:0005343	increased circulating aspartate transaminase level	Daam2<tm1b(KOMP)Wtsi>/Daam2<tm1b(KOMP)Wtsi>	C57BL/6N-Daam2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756952	M	MP:0008806	increased circulating amylase level	Daam2<tm1b(KOMP)Wtsi>/Daam2<tm1b(KOMP)Wtsi>	C57BL/6N-Daam2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756952	F	MP:0002941	increased circulating alanine transaminase level	Daam2<tm1b(KOMP)Wtsi>/Daam2<tm1b(KOMP)Wtsi>	C57BL/6N-Daam2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756953	M	MP:0001488	increased startle reflex	Dach1<tm1b(KOMP)Wtsi>/Dach1<+>	B6N(Cg)-Dach1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756953	M	MP:0002941	increased circulating alanine transaminase level	Dach1<tm1b(KOMP)Wtsi>/Dach1<+>	B6N(Cg)-Dach1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756955	M	MP:0002060	abnormal skin morphology	Dact2<tm1b(EUCOMM)Wtsi>/Dact2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dact2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756955	F	MP:0000689	abnormal spleen morphology	Dact2<tm1b(EUCOMM)Wtsi>/Dact2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dact2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756955	M	MP:0002590	increased mean corpuscular volume	Dact2<tm1b(EUCOMM)Wtsi>/Dact2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dact2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756955	M	MP:0011239	abnormal skin coloration	Dact2<tm1b(EUCOMM)Wtsi>/Dact2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dact2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756955	F	MP:0011110	preweaning lethality, incomplete penetrance	Dact2<tm1b(EUCOMM)Wtsi>/Dact2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dact2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756955	F	MP:0011960	abnormal eye anterior chamber depth	Dact2<tm1b(EUCOMM)Wtsi>/Dact2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dact2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756955	M	MP:0000367	abnormal coat/ hair morphology	Dact2<tm1b(EUCOMM)Wtsi>/Dact2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dact2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5756956	M	MP:0005292	improved glucose tolerance	Dact3<tm1b(KOMP)Wtsi>/Dact3<tm1b(KOMP)Wtsi>	C57BL/6N-Dact3<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756956	M	MP:0005419	decreased circulating serum albumin level	Dact3<tm1b(KOMP)Wtsi>/Dact3<tm1b(KOMP)Wtsi>	C57BL/6N-Dact3<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756956	M	MP:0003960	increased lean body mass	Dact3<tm1b(KOMP)Wtsi>/Dact3<tm1b(KOMP)Wtsi>	C57BL/6N-Dact3<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756957	M	MP:0002188	small heart	Dagla<tm1a(EUCOMM)Wtsi>/Dagla<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dagla<tm1a(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756957	M	MP:0002691	small stomach	Dagla<tm1a(EUCOMM)Wtsi>/Dagla<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dagla<tm1a(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756957	M	MP:0000706	small thymus	Dagla<tm1a(EUCOMM)Wtsi>/Dagla<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dagla<tm1a(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756957	M	MP:0000774	decreased brain size	Dagla<tm1a(EUCOMM)Wtsi>/Dagla<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dagla<tm1a(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756957	M	MP:0000692	small spleen	Dagla<tm1a(EUCOMM)Wtsi>/Dagla<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dagla<tm1a(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756957	M	MP:0004924	abnormal behavior	Dagla<tm1a(EUCOMM)Wtsi>/Dagla<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dagla<tm1a(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756957	M	MP:0000601	small liver	Dagla<tm1a(EUCOMM)Wtsi>/Dagla<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dagla<tm1a(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756957	M	MP:0003641	small lung	Dagla<tm1a(EUCOMM)Wtsi>/Dagla<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dagla<tm1a(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756957	F	MP:0001258	decreased body length	Dagla<tm1a(EUCOMM)Wtsi>/Dagla<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dagla<tm1a(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5756958	F	MP:0001406	abnormal gait	Dapk1<tm1b(EUCOMM)Hmgu>/Dapk1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dapk1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756959	M	MP:0000137	abnormal vertebrae morphology	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5756960	M	MP:0010123	increased bone mineral content	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756960	M	MP:0001566	increased circulating phosphate level	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756961	M	MP:0010067	increased red blood cell distribution width	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756961	F	MP:0008935	decreased mean platelet volume	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5756962	M	MP:0003960	increased lean body mass	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756962	M	MP:0005419	decreased circulating serum albumin level	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756962	M	MP:0002702	decreased circulating free fatty acids level	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5756963	M	MP:0010053	decreased grip strength	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5756970	M	MP:0011100	preweaning lethality, complete penetrance	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<tm1b(KOMP)Wtsi>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5756971	M	MP:0001147	small testis	Dbndd2<tm1b(EUCOMM)Wtsi>/Dbndd2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dbndd2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5756971	M	MP:0011874	enlarged urinary bladder	Dbndd2<tm1b(EUCOMM)Wtsi>/Dbndd2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dbndd2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5756971	M	MP:0005505	thrombocytosis	Dbndd2<tm1b(EUCOMM)Wtsi>/Dbndd2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dbndd2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5756971	M	MP:0002764	short tibia	Dbndd2<tm1b(EUCOMM)Wtsi>/Dbndd2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dbndd2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5756971	M	MP:0004930	small epididymis	Dbndd2<tm1b(EUCOMM)Wtsi>/Dbndd2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dbndd2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5756972	M	MP:0002833	increased heart weight	Dcp2<tm1b(KOMP)Wtsi>/Dcp2<+>	C57BL/6N-Dcp2<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5756975	M	MP:0000692	small spleen	Ddost<tm1.1(KOMP)Vlcg>/Ddost<+>	C57BL/6N-Ddost<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5756975	M	MP:0002768	small adrenal glands	Ddost<tm1.1(KOMP)Vlcg>/Ddost<+>	C57BL/6N-Ddost<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5756979	M	MP:0010123	increased bone mineral content	Defb14<tm1b(KOMP)Wtsi>/Defb14<tm1b(KOMP)Wtsi>	C57BL/6N-Defb14<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756979	F	MP:0003442	decreased circulating glycerol level	Defb14<tm1b(KOMP)Wtsi>/Defb14<tm1b(KOMP)Wtsi>	C57BL/6N-Defb14<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756979	M	MP:0000062	increased bone mineral density	Defb14<tm1b(KOMP)Wtsi>/Defb14<tm1b(KOMP)Wtsi>	C57BL/6N-Defb14<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756979	F	MP:0010052	increased grip strength	Defb14<tm1b(KOMP)Wtsi>/Defb14<tm1b(KOMP)Wtsi>	C57BL/6N-Defb14<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756980	F	MP:0000280	thin ventricular wall	Defb43<tm1b(KOMP)Wtsi>/Defb43<tm1b(KOMP)Wtsi>	C57BL/6N-Defb43<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5756982	M	MP:0005293	impaired glucose tolerance	Depdc5<tm1b(EUCOMM)Hmgu>/Depdc5<+>	C57BL/6N-Depdc5<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756982	M	MP:0010024	increased total body fat amount	Depdc5<tm1b(EUCOMM)Hmgu>/Depdc5<+>	C57BL/6N-Depdc5<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5756989	F	MP:0002875	decreased erythrocyte cell number	Dhx40<tm1b(KOMP)Wtsi>/Dhx40<tm1b(KOMP)Wtsi>	C57BL/6N-Dhx40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756989	M	MP:0003960	increased lean body mass	Dhx40<tm1b(KOMP)Wtsi>/Dhx40<tm1b(KOMP)Wtsi>	C57BL/6N-Dhx40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756989	M	MP:0001312	abnormal cornea morphology	Dhx40<tm1b(KOMP)Wtsi>/Dhx40<tm1b(KOMP)Wtsi>	C57BL/6N-Dhx40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756989	F	MP:0002874	decreased hemoglobin content	Dhx40<tm1b(KOMP)Wtsi>/Dhx40<tm1b(KOMP)Wtsi>	C57BL/6N-Dhx40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756989	F	MP:0011960	abnormal eye anterior chamber depth	Dhx40<tm1b(KOMP)Wtsi>/Dhx40<tm1b(KOMP)Wtsi>	C57BL/6N-Dhx40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756989	F	MP:0011965	decreased total retina thickness	Dhx40<tm1b(KOMP)Wtsi>/Dhx40<tm1b(KOMP)Wtsi>	C57BL/6N-Dhx40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756989	M	MP:0004952	increased spleen weight	Dhx40<tm1b(KOMP)Wtsi>/Dhx40<tm1b(KOMP)Wtsi>	C57BL/6N-Dhx40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756989	F	MP:0000208	decreased hematocrit	Dhx40<tm1b(KOMP)Wtsi>/Dhx40<tm1b(KOMP)Wtsi>	C57BL/6N-Dhx40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5756990	M	MP:0002546	mydriasis	Diaph3<tm1b(KOMP)Mbp>/Diaph3<+>	C57BL/6N-Diaph3<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5756990	M	MP:0002591	decreased mean corpuscular volume	Diaph3<tm1b(KOMP)Mbp>/Diaph3<+>	C57BL/6N-Diaph3<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5756990	M	MP:0002644	decreased circulating triglyceride level	Diaph3<tm1b(KOMP)Mbp>/Diaph3<+>	C57BL/6N-Diaph3<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5756991	M	MP:0000288	abnormal pericardium morphology	Diaph3<tm1b(KOMP)Mbp>/Diaph3<tm1b(KOMP)Mbp>	C57BL/6N-Diaph3<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5756992	F	MP:0001325	abnormal retina morphology	Dicer1<tm1b(EUCOMM)Wtsi>/Dicer1<+>	C57BL/6N-Dicer1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756992	M	MP:0010068	decreased red blood cell distribution width	Dicer1<tm1b(EUCOMM)Wtsi>/Dicer1<+>	C57BL/6N-Dicer1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756992	M	MP:0000222	decreased neutrophil cell number	Dicer1<tm1b(EUCOMM)Wtsi>/Dicer1<+>	C57BL/6N-Dicer1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756992	M	MP:0000690	absent spleen	Dicer1<tm1b(EUCOMM)Wtsi>/Dicer1<+>	C57BL/6N-Dicer1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756992	M	MP:0003961	decreased lean body mass	Dicer1<tm1b(EUCOMM)Wtsi>/Dicer1<+>	C57BL/6N-Dicer1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756992	M	MP:0010053	decreased grip strength	Dicer1<tm1b(EUCOMM)Wtsi>/Dicer1<+>	C57BL/6N-Dicer1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5756994	F	MP:0005293	impaired glucose tolerance	Dis3<tm1e.1(EUCOMM)Hmgu>/Dis3<+>	C57BL/6N-Dis3<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756994	M	MP:0002699	abnormal vitreous body morphology	Dis3<tm1e.1(EUCOMM)Hmgu>/Dis3<+>	C57BL/6N-Dis3<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756994	F	MP:0001325	abnormal retina morphology	Dis3<tm1e.1(EUCOMM)Hmgu>/Dis3<+>	C57BL/6N-Dis3<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756994	M	MP:0001488	increased startle reflex	Dis3<tm1e.1(EUCOMM)Hmgu>/Dis3<+>	C57BL/6N-Dis3<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5756997	F	MP:0005568	increased circulating total protein level	Dnaaf2<tm1.1(KOMP)Vlcg>/Dnaaf2<+>	C57BL/6N-Dnaaf2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756997	F	MP:0005633	increased circulating sodium level	Dnaaf2<tm1.1(KOMP)Vlcg>/Dnaaf2<+>	C57BL/6N-Dnaaf2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756997	M	MP:0011396	abnormal sleep behavior	Dnaaf2<tm1.1(KOMP)Vlcg>/Dnaaf2<+>	C57BL/6N-Dnaaf2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756999	M	MP:0010052	increased grip strength	Dnaja1<tm1.1(KOMP)Vlcg>/Dnaja1<+>	C57BL/6N-Dnaja1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756999	M	MP:0005633	increased circulating sodium level	Dnaja1<tm1.1(KOMP)Vlcg>/Dnaja1<+>	C57BL/6N-Dnaja1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756999	M	MP:0001488	increased startle reflex	Dnaja1<tm1.1(KOMP)Vlcg>/Dnaja1<+>	C57BL/6N-Dnaja1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756999	F	MP:0001399	hyperactivity	Dnaja1<tm1.1(KOMP)Vlcg>/Dnaja1<+>	C57BL/6N-Dnaja1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5756999	F	MP:0010053	decreased grip strength	Dnaja1<tm1.1(KOMP)Vlcg>/Dnaja1<+>	C57BL/6N-Dnaja1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757000	F	MP:0005559	increased circulating glucose level	Dnajc15<tm1b(KOMP)Wtsi>/Dnajc15<tm1b(KOMP)Wtsi>	C57BL/6N-Dnajc15<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757000	F	MP:0004509	abnormal pelvic girdle bone morphology	Dnajc15<tm1b(KOMP)Wtsi>/Dnajc15<tm1b(KOMP)Wtsi>	C57BL/6N-Dnajc15<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757000	M	MP:0000689	abnormal spleen morphology	Dnajc15<tm1b(KOMP)Wtsi>/Dnajc15<tm1b(KOMP)Wtsi>	C57BL/6N-Dnajc15<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757002	F	MP:0003900	shortened QT interval	Dnajc5b<tm1b(EUCOMM)Hmgu>/Dnajc5b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dnajc5b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757002	M	MP:0001417	decreased exploration in new environment	Dnajc5b<tm1b(EUCOMM)Hmgu>/Dnajc5b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dnajc5b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757002	F	MP:0010571	shortened ST segment	Dnajc5b<tm1b(EUCOMM)Hmgu>/Dnajc5b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dnajc5b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757003	F	MP:0002591	decreased mean corpuscular volume	Dnajc7<tm1b(KOMP)Wtsi>/Dnajc7<tm1b(KOMP)Wtsi>	C57BL/6N-Dnajc7<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757003	F	MP:0005562	decreased mean corpuscular hemoglobin	Dnajc7<tm1b(KOMP)Wtsi>/Dnajc7<tm1b(KOMP)Wtsi>	C57BL/6N-Dnajc7<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757004	F	MP:0001417	decreased exploration in new environment	Dnal4<tm1b(EUCOMM)Wtsi>/Dnal4<+>	C57BL/6N-Dnal4<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757006	M	MP:0002110	abnormal digit morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757006	M	MP:0006203	eye hemorrhage	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757006	M	MP:0003961	decreased lean body mass	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757006	F	MP:0003795	abnormal bone structure	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757006	M	MP:0010053	decreased grip strength	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757006	M	MP:0010024	increased total body fat amount	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757006	M	MP:0004174	abnormal spine curvature	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757006	F	MP:0005343	increased circulating aspartate transaminase level	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757006	M	MP:0004613	fusion of vertebral arches	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757006	F	MP:0002932	abnormal joint morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757007	F	MP:0002764	short tibia	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757007	F	MP:0010053	decreased grip strength	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757007	F	MP:0010124	decreased bone mineral content	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757007	F	MP:0008259	abnormal optic disk morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757007	M	MP:0002092	abnormal eye morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757007	F	MP:0001258	decreased body length	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757007	F	MP:0003795	abnormal bone structure	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757008	M	MP:0005565	increased blood urea nitrogen level	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757008	F	MP:0001529	abnormal vocalization	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757008	M	MP:0000572	abnormal autopod morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757008	M	MP:0001304	cataract	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757008	M	MP:0008259	abnormal optic disk morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757008	F	MP:0013279	increased fasting circulating glucose level	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757009	F	MP:0003795	abnormal bone structure	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757009	M	MP:0002111	abnormal tail morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757009	F	MP:0004609	vertebral fusion	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757010	F	MP:0002111	abnormal tail morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:5757010	M	MP:0000432	abnormal head morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:5757010	M	MP:0000194	increased circulating calcium level	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:5757010	F	MP:0000579	abnormal nail morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:5757011	F	MP:0013279	increased fasting circulating glucose level	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757012	F	MP:0000367	abnormal coat/ hair morphology	Dnm1l<tm1b(KOMP)Wtsi>/Dnm1l<+>	C57BL/6N-Dnm1l<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757012	M	MP:0002699	abnormal vitreous body morphology	Dnm1l<tm1b(KOMP)Wtsi>/Dnm1l<+>	C57BL/6N-Dnm1l<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757014	M	MP:0003063	increased coping response	Dntt<tm2b(KOMP)Wtsi>/Dntt<tm2b(KOMP)Wtsi>	C57BL/6N-Dntt<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757014	F	MP:0005178	increased circulating cholesterol level	Dntt<tm2b(KOMP)Wtsi>/Dntt<tm2b(KOMP)Wtsi>	C57BL/6N-Dntt<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757017	M	MP:0005293	impaired glucose tolerance	Dpm2<tm1b(EUCOMM)Hmgu>/Dpm2<+>	C57BL/6N-Dpm2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757017	M	MP:0000274	enlarged heart	Dpm2<tm1b(EUCOMM)Hmgu>/Dpm2<+>	C57BL/6N-Dpm2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757017	M	MP:0005568	increased circulating total protein level	Dpm2<tm1b(EUCOMM)Hmgu>/Dpm2<+>	C57BL/6N-Dpm2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757019	F	MP:0004924	abnormal behavior	Dpp9<tm1b(EUCOMM)Hmgu>/Dpp9<+>	C57BL/6N-Dpp9<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757019	F	MP:0002797	increased thigmotaxis	Dpp9<tm1b(EUCOMM)Hmgu>/Dpp9<+>	C57BL/6N-Dpp9<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757019	F	MP:0001303	abnormal lens morphology	Dpp9<tm1b(EUCOMM)Hmgu>/Dpp9<+>	C57BL/6N-Dpp9<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757019	F	MP:0001363	increased anxiety-related response	Dpp9<tm1b(EUCOMM)Hmgu>/Dpp9<+>	C57BL/6N-Dpp9<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757021	M	MP:0000689	abnormal spleen morphology	Dppa1<tm1b(KOMP)Wtsi>/Dppa1<+>	C57BL/6N-Dppa1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757023	M	MP:0002631	abnormal epididymis morphology	Dpyd<tm1b(KOMP)Wtsi>/Dpyd<tm1b(KOMP)Wtsi>	C57BL/6N-Dpyd<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757023	F	MP:0000470	abnormal stomach morphology	Dpyd<tm1b(KOMP)Wtsi>/Dpyd<tm1b(KOMP)Wtsi>	C57BL/6N-Dpyd<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757025	F	MP:0010053	decreased grip strength	Dtnbp1<tm1b(EUCOMM)Hmgu>/Dtnbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dtnbp1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757025	M	MP:0011110	preweaning lethality, incomplete penetrance	Dtnbp1<tm1b(EUCOMM)Hmgu>/Dtnbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dtnbp1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757025	F	MP:0013279	increased fasting circulating glucose level	Dtnbp1<tm1b(EUCOMM)Hmgu>/Dtnbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dtnbp1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757025	F	MP:0000218	increased leukocyte cell number	Dtnbp1<tm1b(EUCOMM)Hmgu>/Dtnbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dtnbp1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757025	M	MP:0005016	decreased lymphocyte cell number	Dtnbp1<tm1b(EUCOMM)Hmgu>/Dtnbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dtnbp1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757025	F	MP:0001120	abnormal uterus morphology	Dtnbp1<tm1b(EUCOMM)Hmgu>/Dtnbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dtnbp1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757025	M	MP:0001417	decreased exploration in new environment	Dtnbp1<tm1b(EUCOMM)Hmgu>/Dtnbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dtnbp1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757025	F	MP:0005013	increased lymphocyte cell number	Dtnbp1<tm1b(EUCOMM)Hmgu>/Dtnbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dtnbp1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757026	F	MP:0001392	abnormal locomotor behavior	Dusp11<tm1b(EUCOMM)Wtsi>/Dusp11<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dusp11<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757026	M	MP:0005343	increased circulating aspartate transaminase level	Dusp11<tm1b(EUCOMM)Wtsi>/Dusp11<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dusp11<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757026	M	MP:0010392	prolonged QRS complex duration	Dusp11<tm1b(EUCOMM)Wtsi>/Dusp11<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dusp11<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757027	M	MP:0001488	increased startle reflex	Dusp7<tm1(KOMP)Wtsi>/Dusp7<tm1(KOMP)Wtsi>	C57BL/6N-Dusp7<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757027	M	MP:0002075	abnormal coat/hair pigmentation	Dusp7<tm1(KOMP)Wtsi>/Dusp7<tm1(KOMP)Wtsi>	C57BL/6N-Dusp7<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757027	M	MP:0005179	decreased circulating cholesterol level	Dusp7<tm1(KOMP)Wtsi>/Dusp7<tm1(KOMP)Wtsi>	C57BL/6N-Dusp7<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757027	M	MP:0000186	decreased circulating HDL cholesterol level	Dusp7<tm1(KOMP)Wtsi>/Dusp7<tm1(KOMP)Wtsi>	C57BL/6N-Dusp7<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757027	F	MP:0001926	female infertility	Dusp7<tm1(KOMP)Wtsi>/Dusp7<tm1(KOMP)Wtsi>	C57BL/6N-Dusp7<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757027	M	MP:0002753	dilated heart left ventricle	Dusp7<tm1(KOMP)Wtsi>/Dusp7<tm1(KOMP)Wtsi>	C57BL/6N-Dusp7<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757027	M	MP:0001925	male infertility	Dusp7<tm1(KOMP)Wtsi>/Dusp7<tm1(KOMP)Wtsi>	C57BL/6N-Dusp7<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757029	M	MP:0000222	decreased neutrophil cell number	Ecm1<tm1b(EUCOMM)Hmgu>/Ecm1<+>	C57BL/6N-Ecm1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757031	M	MP:0000745	tremors	Ect2<tm1b(EUCOMM)Wtsi>/Ect2<+>	C57BL/6N-Ect2<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757033	F	MP:0009709	hydrometra	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	F	MP:0001314	cornea opacity	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	M	MP:0001402	decreased locomotor activity	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	M	MP:0010053	decreased grip strength	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	F	MP:0001303	abnormal lens morphology	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	M	MP:0001399	hyperactivity	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	M	MP:0008528	polycystic kidney	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	F	MP:0001304	cataract	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	M	MP:0013279	increased fasting circulating glucose level	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	F	MP:0001319	irregularly shaped pupil	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	F	MP:0003068	enlarged kidney	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	F	MP:0004906	enlarged uterus	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	M	MP:0001925	male infertility	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	F	MP:0000642	enlarged adrenal glands	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757033	F	MP:0001312	abnormal cornea morphology	Efna5<tm1b(EUCOMM)Wtsi>/Efna5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Efna5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757034	F	MP:0001417	decreased exploration in new environment	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757034	F	MP:0004924	abnormal behavior	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757034	M	MP:0005554	decreased circulating creatinine level	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757034	M	MP:0002599	increased mean platelet volume	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757034	F	MP:0010052	increased grip strength	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757034	M	MP:0005566	decreased blood urea nitrogen level	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757034	M	MP:0005419	decreased circulating serum albumin level	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757034	F	MP:0001314	cornea opacity	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757034	F	MP:0001363	increased anxiety-related response	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757034	M	MP:0003960	increased lean body mass	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757034	M	MP:0000219	increased neutrophil cell number	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757034	F	MP:0002797	increased thigmotaxis	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757035	F	MP:0005562	decreased mean corpuscular hemoglobin	Eif2b3<tm1b(EUCOMM)Hmgu>/Eif2b3<+>	C57BL/6N-Eif2b3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757037	M	MP:0005293	impaired glucose tolerance	Eif4g2<tm1b(KOMP)Wtsi>/Eif4g2<+>	C57BL/6N-Eif4g2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757037	F	MP:0003795	abnormal bone structure	Eif4g2<tm1b(KOMP)Wtsi>/Eif4g2<+>	C57BL/6N-Eif4g2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757037	F	MP:0000063	decreased bone mineral density	Eif4g2<tm1b(KOMP)Wtsi>/Eif4g2<+>	C57BL/6N-Eif4g2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757037	F	MP:0013279	increased fasting circulating glucose level	Eif4g2<tm1b(KOMP)Wtsi>/Eif4g2<+>	C57BL/6N-Eif4g2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757037	F	MP:0010124	decreased bone mineral content	Eif4g2<tm1b(KOMP)Wtsi>/Eif4g2<+>	C57BL/6N-Eif4g2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757037	F	MP:0005560	decreased circulating glucose level	Eif4g2<tm1b(KOMP)Wtsi>/Eif4g2<+>	C57BL/6N-Eif4g2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757039	F	MP:0020870	decreased thigmotaxis	Elfn1<tm1.1(KOMP)Vlcg>/Elfn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Elfn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757039	F	MP:0001399	hyperactivity	Elfn1<tm1.1(KOMP)Vlcg>/Elfn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Elfn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757039	F	MP:0004924	abnormal behavior	Elfn1<tm1.1(KOMP)Vlcg>/Elfn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Elfn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757039	F	MP:0000955	abnormal spinal cord morphology	Elfn1<tm1.1(KOMP)Vlcg>/Elfn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Elfn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757040	M	MP:0005016	decreased lymphocyte cell number	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	M	MP:0011954	shortened PQ interval	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	M	MP:0002833	increased heart weight	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	M	MP:0010511	shortened PR interval	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	M	MP:0003917	increased kidney weight	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	M	MP:0001322	abnormal iris morphology	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	F	MP:0005565	increased blood urea nitrogen level	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	M	MP:0000223	decreased monocyte cell number	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	F	MP:0002590	increased mean corpuscular volume	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	F	MP:0004953	decreased spleen weight	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	M	MP:0001489	decreased startle reflex	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	M	MP:0000221	decreased leukocyte cell number	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	F	MP:0005561	increased mean corpuscular hemoglobin	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	M	MP:0010067	increased red blood cell distribution width	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757040	M	MP:0001566	increased circulating phosphate level	Elmod1<tm1b(EUCOMM)Hmgu>/Elmod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757041	F	MP:0005633	increased circulating sodium level	Elof1<tm1.1(KOMP)Vlcg>/Elof1<+>	C57BL/6N-Elof1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757041	M	MP:0005419	decreased circulating serum albumin level	Elof1<tm1.1(KOMP)Vlcg>/Elof1<+>	C57BL/6N-Elof1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757043	F	MP:0001529	abnormal vocalization	Emc10<tm1b(EUCOMM)Wtsi>/Emc10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Emc10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757043	F	MP:0001406	abnormal gait	Emc10<tm1b(EUCOMM)Wtsi>/Emc10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Emc10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757043	F	MP:0000280	thin ventricular wall	Emc10<tm1b(EUCOMM)Wtsi>/Emc10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Emc10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757043	F	MP:0001392	abnormal locomotor behavior	Emc10<tm1b(EUCOMM)Wtsi>/Emc10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Emc10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757043	F	MP:0013278	decreased fasting circulating glucose level	Emc10<tm1b(EUCOMM)Wtsi>/Emc10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Emc10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757044	M	MP:0002606	increased basophil cell number	Emc4<tm1(KOMP)Wtsi>/Emc4<+>	C57BL/6N-Emc4<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757044	F	MP:0013279	increased fasting circulating glucose level	Emc4<tm1(KOMP)Wtsi>/Emc4<+>	C57BL/6N-Emc4<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757044	M	MP:0005011	increased eosinophil cell number	Emc4<tm1(KOMP)Wtsi>/Emc4<+>	C57BL/6N-Emc4<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757044	F	MP:0002075	abnormal coat/hair pigmentation	Emc4<tm1(KOMP)Wtsi>/Emc4<+>	C57BL/6N-Emc4<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757044	F	MP:0010580	decreased heart left ventricle size	Emc4<tm1(KOMP)Wtsi>/Emc4<+>	C57BL/6N-Emc4<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757045	F	MP:0005633	increased circulating sodium level	Entpd1<tm1b(EUCOMM)Wtsi>/Entpd1<+>	C57BL/6N-Entpd1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757047	M	MP:0003961	decreased lean body mass	Eomes<tm1b(EUCOMM)Wtsi>/Eomes<+>	C57BL/6N-Eomes<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757047	M	MP:0005554	decreased circulating creatinine level	Eomes<tm1b(EUCOMM)Wtsi>/Eomes<+>	C57BL/6N-Eomes<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757049	F	MP:0000266	abnormal heart morphology	Epas1<tm1b(EUCOMM)Hmgu>/Epas1<+>	C57BL/6N-Epas1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757051	F	MP:0001258	decreased body length	Epb41l4b<tm1b(EUCOMM)Hmgu>/Epb41l4b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Epb41l4b<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5757053	M	MP:0001304	cataract	Epc2<tm1b(EUCOMM)Wtsi>/Epc2<+>	C57BL/6N-Epc2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757053	M	MP:0001402	decreased locomotor activity	Epc2<tm1b(EUCOMM)Wtsi>/Epc2<+>	C57BL/6N-Epc2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757053	M	MP:0002797	increased thigmotaxis	Epc2<tm1b(EUCOMM)Wtsi>/Epc2<+>	C57BL/6N-Epc2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757053	F	MP:0010378	increased respiratory quotient	Epc2<tm1b(EUCOMM)Wtsi>/Epc2<+>	C57BL/6N-Epc2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757053	F	MP:0001325	abnormal retina morphology	Epc2<tm1b(EUCOMM)Wtsi>/Epc2<+>	C57BL/6N-Epc2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757053	M	MP:0004924	abnormal behavior	Epc2<tm1b(EUCOMM)Wtsi>/Epc2<+>	C57BL/6N-Epc2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757053	M	MP:0010097	abnormal retina blood vessel morphology	Epc2<tm1b(EUCOMM)Wtsi>/Epc2<+>	C57BL/6N-Epc2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757057	F	MP:0000455	abnormal maxilla morphology	Eps8l3<tm1b(KOMP)Mbp>/Eps8l3<tm1b(KOMP)Mbp>	C57BL/6N-Eps8l3<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757057	F	MP:0000438	abnormal cranium morphology	Eps8l3<tm1b(KOMP)Mbp>/Eps8l3<tm1b(KOMP)Mbp>	C57BL/6N-Eps8l3<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757058	M	MP:0005633	increased circulating sodium level	Espnl<tm1b(KOMP)Wtsi>/Espnl<tm1b(KOMP)Wtsi>	C57BL/6N-Espnl<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757059	M	MP:0002590	increased mean corpuscular volume	Esyt3<tm1b(EUCOMM)Wtsi>/Esyt3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Esyt3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757059	M	MP:0002875	decreased erythrocyte cell number	Esyt3<tm1b(EUCOMM)Wtsi>/Esyt3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Esyt3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757059	M	MP:0002941	increased circulating alanine transaminase level	Esyt3<tm1b(EUCOMM)Wtsi>/Esyt3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Esyt3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757060	M	MP:0013279	increased fasting circulating glucose level	Evl<tm1b(KOMP)Wtsi>/Evl<tm1b(KOMP)Wtsi>	C57BL/6N-Evl<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757060	M	MP:0005505	thrombocytosis	Evl<tm1b(KOMP)Wtsi>/Evl<tm1b(KOMP)Wtsi>	C57BL/6N-Evl<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757061	M	MP:0001399	hyperactivity	Ewsr1<tm1b(EUCOMM)Wtsi>/Ewsr1<+>	C57BL/6N-Ewsr1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757061	F	MP:0002764	short tibia	Ewsr1<tm1b(EUCOMM)Wtsi>/Ewsr1<+>	C57BL/6N-Ewsr1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757061	M	MP:0010052	increased grip strength	Ewsr1<tm1b(EUCOMM)Wtsi>/Ewsr1<+>	C57BL/6N-Ewsr1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757061	F	MP:0002968	increased circulating alkaline phosphatase level	Ewsr1<tm1b(EUCOMM)Wtsi>/Ewsr1<+>	C57BL/6N-Ewsr1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757063	F	MP:0008810	increased circulating iron level	Exoc3l2<tm1b(KOMP)Wtsi>/Exoc3l2<+>	C57BL/6N-Exoc3l2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757065	M	MP:0002768	small adrenal glands	Eya4<tm1b(KOMP)Wtsi>/Eya4<+>	C57BL/6N-Eya4<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757067	F	MP:0002875	decreased erythrocyte cell number	Ezh1<tm1b(EUCOMM)Wtsi>/Ezh1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ezh1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757067	M	MP:0009142	decreased prepulse inhibition	Ezh1<tm1b(EUCOMM)Wtsi>/Ezh1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ezh1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757067	F	MP:0000208	decreased hematocrit	Ezh1<tm1b(EUCOMM)Wtsi>/Ezh1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ezh1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757067	M	MP:0001925	male infertility	Ezh1<tm1b(EUCOMM)Wtsi>/Ezh1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ezh1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757067	M	MP:0010068	decreased red blood cell distribution width	Ezh1<tm1b(EUCOMM)Wtsi>/Ezh1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ezh1<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757071	M	MP:0000443	abnormal snout morphology	F7<tm1b(EUCOMM)Hmgu>/F7<+>	C57BL/6N-F7<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757071	M	MP:0003961	decreased lean body mass	F7<tm1b(EUCOMM)Hmgu>/F7<+>	C57BL/6N-F7<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757071	M	MP:0010124	decreased bone mineral content	F7<tm1b(EUCOMM)Hmgu>/F7<+>	C57BL/6N-F7<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757071	M	MP:0010024	increased total body fat amount	F7<tm1b(EUCOMM)Hmgu>/F7<+>	C57BL/6N-F7<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757073	M	MP:0005016	decreased lymphocyte cell number	Fabp1<tm1b(EUCOMM)Hmgu>/Fabp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fabp1<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757073	M	MP:0012361	decreased large unstained cell number	Fabp1<tm1b(EUCOMM)Hmgu>/Fabp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fabp1<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757073	F	MP:0005344	increased circulating bilirubin level	Fabp1<tm1b(EUCOMM)Hmgu>/Fabp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fabp1<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757073	M	MP:0000221	decreased leukocyte cell number	Fabp1<tm1b(EUCOMM)Hmgu>/Fabp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fabp1<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757074	F	MP:0001120	abnormal uterus morphology	Fadd<tm1e.1(KOMP)Wtsi>/Fadd<+>	C57BL/6N-Fadd<tm1e.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757074	M	MP:0003961	decreased lean body mass	Fadd<tm1e.1(KOMP)Wtsi>/Fadd<+>	C57BL/6N-Fadd<tm1e.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757074	M	MP:0010024	increased total body fat amount	Fadd<tm1e.1(KOMP)Wtsi>/Fadd<+>	C57BL/6N-Fadd<tm1e.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757077	M	MP:0005343	increased circulating aspartate transaminase level	Retreg3<tm2b(EUCOMM)Wtsi>/Retreg3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Fam134c<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757077	F	MP:0008806	increased circulating amylase level	Retreg3<tm2b(EUCOMM)Wtsi>/Retreg3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Fam134c<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757077	F	MP:0002968	increased circulating alkaline phosphatase level	Retreg3<tm2b(EUCOMM)Wtsi>/Retreg3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Fam134c<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757077	F	MP:0005565	increased blood urea nitrogen level	Retreg3<tm2b(EUCOMM)Wtsi>/Retreg3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Fam134c<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757077	F	MP:0003960	increased lean body mass	Retreg3<tm2b(EUCOMM)Wtsi>/Retreg3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Fam134c<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757077	F	MP:0009142	decreased prepulse inhibition	Retreg3<tm2b(EUCOMM)Wtsi>/Retreg3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Fam134c<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757077	M	MP:0001552	increased circulating triglyceride level	Retreg3<tm2b(EUCOMM)Wtsi>/Retreg3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Fam134c<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757079	M	MP:0000219	increased neutrophil cell number	Fam151b<tm1b(EUCOMM)Hmgu>/Fam151b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fam151b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757080	M	MP:0001488	increased startle reflex	Fam161a<tm1b(KOMP)Wtsi>/Fam161a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam161a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757080	M	MP:0003960	increased lean body mass	Fam161a<tm1b(KOMP)Wtsi>/Fam161a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam161a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757080	M	MP:0003064	decreased coping response	Fam161a<tm1b(KOMP)Wtsi>/Fam161a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam161a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757080	M	MP:0002833	increased heart weight	Fam161a<tm1b(KOMP)Wtsi>/Fam161a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam161a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757080	F	MP:0005633	increased circulating sodium level	Fam161a<tm1b(KOMP)Wtsi>/Fam161a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam161a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757080	F	MP:0001417	decreased exploration in new environment	Fam161a<tm1b(KOMP)Wtsi>/Fam161a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam161a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757080	M	MP:0008259	abnormal optic disk morphology	Fam161a<tm1b(KOMP)Wtsi>/Fam161a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam161a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757080	M	MP:0000186	decreased circulating HDL cholesterol level	Fam161a<tm1b(KOMP)Wtsi>/Fam161a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam161a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757080	M	MP:0005179	decreased circulating cholesterol level	Fam161a<tm1b(KOMP)Wtsi>/Fam161a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam161a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757080	F	MP:0010052	increased grip strength	Fam161a<tm1b(KOMP)Wtsi>/Fam161a<tm1b(KOMP)Wtsi>	C57BL/6N-Fam161a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757081	M	MP:0001556	increased circulating HDL cholesterol level	Fam186b<tm1b(KOMP)Mbp>/Fam186b<tm1b(KOMP)Mbp>	C57BL/6N-Fam186b<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757081	M	MP:0005633	increased circulating sodium level	Fam186b<tm1b(KOMP)Mbp>/Fam186b<tm1b(KOMP)Mbp>	C57BL/6N-Fam186b<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757081	M	MP:0013279	increased fasting circulating glucose level	Fam186b<tm1b(KOMP)Mbp>/Fam186b<tm1b(KOMP)Mbp>	C57BL/6N-Fam186b<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757083	F	MP:0010052	increased grip strength	Tent5c<tm1b(KOMP)Wtsi>/Tent5c<+>	C57BL/6N-Tent5c<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757085	F	MP:0001417	decreased exploration in new environment	Cyrib<tm1b(KOMP)Wtsi>/Cyrib<+>	C57BL/6N-Cyrib<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757085	M	MP:0005634	decreased circulating sodium level	Cyrib<tm1b(KOMP)Wtsi>/Cyrib<+>	C57BL/6N-Cyrib<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757086	M	MP:0001925	male infertility	Cyrib<tm1b(KOMP)Wtsi>/Cyrib<tm1b(KOMP)Wtsi>	C57BL/6N-Cyrib<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757087	F	MP:0009142	decreased prepulse inhibition	Fam53b<tm1b(EUCOMM)Hmgu>/Fam53b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fam53b<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757087	F	MP:0005633	increased circulating sodium level	Fam53b<tm1b(EUCOMM)Hmgu>/Fam53b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fam53b<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757087	F	MP:0011951	increased cardiac stroke volume	Fam53b<tm1b(EUCOMM)Hmgu>/Fam53b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fam53b<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757087	M	MP:0010068	decreased red blood cell distribution width	Fam53b<tm1b(EUCOMM)Hmgu>/Fam53b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fam53b<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757089	M	MP:0001304	cataract	Miga1<tm1b(EUCOMM)Wtsi>/Miga1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Miga1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757090	F	MP:0003961	decreased lean body mass	Fancl<tm1b(EUCOMM)Hmgu>/Fancl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fancl<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757090	F	MP:0002606	increased basophil cell number	Fancl<tm1b(EUCOMM)Hmgu>/Fancl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fancl<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757090	F	MP:0005011	increased eosinophil cell number	Fancl<tm1b(EUCOMM)Hmgu>/Fancl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fancl<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757090	F	MP:0000063	decreased bone mineral density	Fancl<tm1b(EUCOMM)Hmgu>/Fancl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fancl<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757090	F	MP:0001258	decreased body length	Fancl<tm1b(EUCOMM)Hmgu>/Fancl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fancl<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757090	F	MP:0010024	increased total body fat amount	Fancl<tm1b(EUCOMM)Hmgu>/Fancl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fancl<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757090	F	MP:0003795	abnormal bone structure	Fancl<tm1b(EUCOMM)Hmgu>/Fancl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fancl<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757090	F	MP:0010124	decreased bone mineral content	Fancl<tm1b(EUCOMM)Hmgu>/Fancl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fancl<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757091	F	MP:0002792	abnormal retina vasculature morphology	Fbp2<tm2b(EUCOMM)Hmgu>/Fbp2<+>	C57BL/6N-Fbp2<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757091	F	MP:0010097	abnormal retina blood vessel morphology	Fbp2<tm2b(EUCOMM)Hmgu>/Fbp2<+>	C57BL/6N-Fbp2<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757092	M	MP:0001303	abnormal lens morphology	Fbp2<tm2b(EUCOMM)Hmgu>/Fbp2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Fbp2<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757095	M	MP:0002606	increased basophil cell number	Fbxl19<tm1b(EUCOMM)Wtsi>/Fbxl19<+>	C57BL/6N-Fbxl19<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757095	M	MP:0000220	increased monocyte cell number	Fbxl19<tm1b(EUCOMM)Wtsi>/Fbxl19<+>	C57BL/6N-Fbxl19<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757095	M	MP:0000218	increased leukocyte cell number	Fbxl19<tm1b(EUCOMM)Wtsi>/Fbxl19<+>	C57BL/6N-Fbxl19<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757095	M	MP:0005011	increased eosinophil cell number	Fbxl19<tm1b(EUCOMM)Wtsi>/Fbxl19<+>	C57BL/6N-Fbxl19<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757095	M	MP:0005560	decreased circulating glucose level	Fbxl19<tm1b(EUCOMM)Wtsi>/Fbxl19<+>	C57BL/6N-Fbxl19<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757095	M	MP:0000219	increased neutrophil cell number	Fbxl19<tm1b(EUCOMM)Wtsi>/Fbxl19<+>	C57BL/6N-Fbxl19<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757095	M	MP:0005016	decreased lymphocyte cell number	Fbxl19<tm1b(EUCOMM)Wtsi>/Fbxl19<+>	C57BL/6N-Fbxl19<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757095	M	MP:0002599	increased mean platelet volume	Fbxl19<tm1b(EUCOMM)Wtsi>/Fbxl19<+>	C57BL/6N-Fbxl19<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757095	M	MP:0005567	decreased circulating total protein level	Fbxl19<tm1b(EUCOMM)Wtsi>/Fbxl19<+>	C57BL/6N-Fbxl19<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757099	F	MP:0001402	decreased locomotor activity	Fbxo2<tm1b(EUCOMM)Wtsi>/Fbxo2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fbxo2<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757099	F	MP:0013278	decreased fasting circulating glucose level	Fbxo2<tm1b(EUCOMM)Wtsi>/Fbxo2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fbxo2<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757101	F	MP:0006358	absent pinna reflex	Fbxo33<tm1b(EUCOMM)Wtsi>/Fbxo33<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fbxo33<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757101	F	MP:0002941	increased circulating alanine transaminase level	Fbxo33<tm1b(EUCOMM)Wtsi>/Fbxo33<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fbxo33<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757102	F	MP:0000274	enlarged heart	Fbxo44<tm1b(KOMP)Wtsi>/Fbxo44<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo44<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757102	F	MP:0010053	decreased grip strength	Fbxo44<tm1b(KOMP)Wtsi>/Fbxo44<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo44<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757102	F	MP:0000266	abnormal heart morphology	Fbxo44<tm1b(KOMP)Wtsi>/Fbxo44<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo44<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757103	M	MP:0002768	small adrenal glands	Fbxo9<tm1b(EUCOMM)Hmgu>/Fbxo9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fbxo9<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757103	M	MP:0001556	increased circulating HDL cholesterol level	Fbxo9<tm1b(EUCOMM)Hmgu>/Fbxo9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fbxo9<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757103	M	MP:0005011	increased eosinophil cell number	Fbxo9<tm1b(EUCOMM)Hmgu>/Fbxo9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fbxo9<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757103	M	MP:0002606	increased basophil cell number	Fbxo9<tm1b(EUCOMM)Hmgu>/Fbxo9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fbxo9<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757103	F	MP:0001417	decreased exploration in new environment	Fbxo9<tm1b(EUCOMM)Hmgu>/Fbxo9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fbxo9<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757103	M	MP:0009142	decreased prepulse inhibition	Fbxo9<tm1b(EUCOMM)Hmgu>/Fbxo9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fbxo9<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757105	M	MP:0000219	increased neutrophil cell number	Fbxw8<tm1b(EUCOMM)Hmgu>/Fbxw8<+>	C57BL/6N-Fbxw8<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757105	M	MP:0005016	decreased lymphocyte cell number	Fbxw8<tm1b(EUCOMM)Hmgu>/Fbxw8<+>	C57BL/6N-Fbxw8<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757105	M	MP:0005011	increased eosinophil cell number	Fbxw8<tm1b(EUCOMM)Hmgu>/Fbxw8<+>	C57BL/6N-Fbxw8<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757105	M	MP:0005565	increased blood urea nitrogen level	Fbxw8<tm1b(EUCOMM)Hmgu>/Fbxw8<+>	C57BL/6N-Fbxw8<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757105	M	MP:0002606	increased basophil cell number	Fbxw8<tm1b(EUCOMM)Hmgu>/Fbxw8<+>	C57BL/6N-Fbxw8<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757105	M	MP:0005553	increased circulating creatinine level	Fbxw8<tm1b(EUCOMM)Hmgu>/Fbxw8<+>	C57BL/6N-Fbxw8<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757107	F	MP:0000690	absent spleen	Fbxw9<tm1a(EUCOMM)Wtsi>/Fbxw9<+>	C57BL/6N-Fbxw9<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757108	M	MP:0000681	abnormal thyroid gland morphology	Fbxw9<tm1a(EUCOMM)Wtsi>/Fbxw9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbxw9<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757108	M	MP:0002282	abnormal trachea morphology	Fbxw9<tm1a(EUCOMM)Wtsi>/Fbxw9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbxw9<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757108	M	MP:0008024	absent lymph nodes	Fbxw9<tm1a(EUCOMM)Wtsi>/Fbxw9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbxw9<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757108	M	MP:0001293	anophthalmia	Fbxw9<tm1a(EUCOMM)Wtsi>/Fbxw9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbxw9<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757108	F	MP:0011100	preweaning lethality, complete penetrance	Fbxw9<tm1a(EUCOMM)Wtsi>/Fbxw9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fbxw9<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757109	M	MP:0010052	increased grip strength	Fdx1<tm1b(EUCOMM)Wtsi>/Fdx1<+>	C57BL/6N-Fdx1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757109	M	MP:0001325	abnormal retina morphology	Fdx1<tm1b(EUCOMM)Wtsi>/Fdx1<+>	C57BL/6N-Fdx1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757111	M	MP:0001399	hyperactivity	Fdxacb1<tm1.1(KOMP)Vlcg>/Fdxacb1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fdxacb1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757111	F	MP:0005633	increased circulating sodium level	Fdxacb1<tm1.1(KOMP)Vlcg>/Fdxacb1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fdxacb1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757111	F	MP:0000063	decreased bone mineral density	Fdxacb1<tm1.1(KOMP)Vlcg>/Fdxacb1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fdxacb1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757112	F	MP:0001314	cornea opacity	Fgf10<tm1b(EUCOMM)Wtsi>/Fgf10<+>	C57BL/6N-Fgf10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757112	M	MP:0000221	decreased leukocyte cell number	Fgf10<tm1b(EUCOMM)Wtsi>/Fgf10<+>	C57BL/6N-Fgf10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757112	F	MP:0004924	abnormal behavior	Fgf10<tm1b(EUCOMM)Wtsi>/Fgf10<+>	C57BL/6N-Fgf10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757112	F	MP:0020870	decreased thigmotaxis	Fgf10<tm1b(EUCOMM)Wtsi>/Fgf10<+>	C57BL/6N-Fgf10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757112	F	MP:0001402	decreased locomotor activity	Fgf10<tm1b(EUCOMM)Wtsi>/Fgf10<+>	C57BL/6N-Fgf10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757112	F	MP:0006243	impaired pupillary reflex	Fgf10<tm1b(EUCOMM)Wtsi>/Fgf10<+>	C57BL/6N-Fgf10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757112	M	MP:0001556	increased circulating HDL cholesterol level	Fgf10<tm1b(EUCOMM)Wtsi>/Fgf10<+>	C57BL/6N-Fgf10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757112	F	MP:0010053	decreased grip strength	Fgf10<tm1b(EUCOMM)Wtsi>/Fgf10<+>	C57BL/6N-Fgf10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757112	F	MP:0001312	abnormal cornea morphology	Fgf10<tm1b(EUCOMM)Wtsi>/Fgf10<+>	C57BL/6N-Fgf10<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757114	M	MP:0001325	abnormal retina morphology	Fgf2<tm1b(EUCOMM)Wtsi>/Fgf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fgf2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757114	M	MP:0002965	increased circulating serum albumin level	Fgf2<tm1b(EUCOMM)Wtsi>/Fgf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fgf2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757114	M	MP:0001513	limb grasping	Fgf2<tm1b(EUCOMM)Wtsi>/Fgf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fgf2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757114	M	MP:0005568	increased circulating total protein level	Fgf2<tm1b(EUCOMM)Wtsi>/Fgf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fgf2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757117	M	MP:0000274	enlarged heart	Fgf9<tm1b(KOMP)Wtsi>/Fgf9<+>	C57BL/6N-Fgf9<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757120	F	MP:0002968	increased circulating alkaline phosphatase level	Cep43<tm1b(EUCOMM)Hmgu>/Cep43<+>	C57BL/6N-Cep43<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757122	M	MP:0001257	increased body length	Fgfr4<tm1b(EUCOMM)Wtsi>/Fgfr4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fgfr4<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757123	M	MP:0000063	decreased bone mineral density	Flnb<tm1b(KOMP)Wtsi>/Flnb<+>	C57BL/6N-Flnb<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757123	M	MP:0010068	decreased red blood cell distribution width	Flnb<tm1b(KOMP)Wtsi>/Flnb<+>	C57BL/6N-Flnb<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757123	M	MP:0003961	decreased lean body mass	Flnb<tm1b(KOMP)Wtsi>/Flnb<+>	C57BL/6N-Flnb<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757123	M	MP:0010024	increased total body fat amount	Flnb<tm1b(KOMP)Wtsi>/Flnb<+>	C57BL/6N-Flnb<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757123	M	MP:0002965	increased circulating serum albumin level	Flnb<tm1b(KOMP)Wtsi>/Flnb<+>	C57BL/6N-Flnb<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757123	M	MP:0000222	decreased neutrophil cell number	Flnb<tm1b(KOMP)Wtsi>/Flnb<+>	C57BL/6N-Flnb<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757123	M	MP:0010124	decreased bone mineral content	Flnb<tm1b(KOMP)Wtsi>/Flnb<+>	C57BL/6N-Flnb<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757125	M	MP:0011239	abnormal skin coloration	Fmnl3<tm1b(KOMP)Wtsi>/Fmnl3<+>	C57BL/6N-Fmnl3<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757128	M	MP:0003179	thrombocytopenia	Fntb<tm1b(EUCOMM)Hmgu>/Fntb<+>	C57BL/6N-Fntb<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757131	F	MP:0002092	abnormal eye morphology	Foxj3<tm1b(EUCOMM)Wtsi>/Foxj3<+>	C57BL/6N-Foxj3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757131	M	MP:0001510	abnormal coat appearance	Foxj3<tm1b(EUCOMM)Wtsi>/Foxj3<+>	C57BL/6N-Foxj3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757131	M	MP:0010025	decreased total body fat amount	Foxj3<tm1b(EUCOMM)Wtsi>/Foxj3<+>	C57BL/6N-Foxj3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757131	M	MP:0010123	increased bone mineral content	Foxj3<tm1b(EUCOMM)Wtsi>/Foxj3<+>	C57BL/6N-Foxj3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757131	M	MP:0000218	increased leukocyte cell number	Foxj3<tm1b(EUCOMM)Wtsi>/Foxj3<+>	C57BL/6N-Foxj3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757133	M	MP:0005564	increased hemoglobin content	Fpr3<tm1b(EUCOMM)Hmgu>/Fpr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fpr3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757133	M	MP:0002608	increased hematocrit	Fpr3<tm1b(EUCOMM)Hmgu>/Fpr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fpr3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757133	M	MP:0005178	increased circulating cholesterol level	Fpr3<tm1b(EUCOMM)Hmgu>/Fpr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fpr3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757133	M	MP:0002581	abnormal ileum morphology	Fpr3<tm1b(EUCOMM)Hmgu>/Fpr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fpr3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757133	M	MP:0001417	decreased exploration in new environment	Fpr3<tm1b(EUCOMM)Hmgu>/Fpr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fpr3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757133	M	MP:0000495	abnormal colon morphology	Fpr3<tm1b(EUCOMM)Hmgu>/Fpr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fpr3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757134	F	MP:0001303	abnormal lens morphology	Frmd5<tm1b(EUCOMM)Hmgu>/Frmd5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Frmd5<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757134	F	MP:0001926	female infertility	Frmd5<tm1b(EUCOMM)Hmgu>/Frmd5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Frmd5<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757134	F	MP:0001399	hyperactivity	Frmd5<tm1b(EUCOMM)Hmgu>/Frmd5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Frmd5<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757135	M	MP:0001284	absent vibrissae	Frrs1l<tm1b(EUCOMM)Hmgu>/Frrs1l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Frrs1l<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757135	M	MP:0001513	limb grasping	Frrs1l<tm1b(EUCOMM)Hmgu>/Frrs1l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Frrs1l<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757135	M	MP:0001512	trunk curl	Frrs1l<tm1b(EUCOMM)Hmgu>/Frrs1l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Frrs1l<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757135	F	MP:0001399	hyperactivity	Frrs1l<tm1b(EUCOMM)Hmgu>/Frrs1l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Frrs1l<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757135	M	MP:0010053	decreased grip strength	Frrs1l<tm1b(EUCOMM)Hmgu>/Frrs1l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Frrs1l<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757138	M	MP:0001486	abnormal startle reflex	Fshr<tm1(KOMP)Vlcg>/Fshr<tm1(KOMP)Vlcg>	C57BL/6N-Fshr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757138	F	MP:0003961	decreased lean body mass	Fshr<tm1(KOMP)Vlcg>/Fshr<tm1(KOMP)Vlcg>	C57BL/6N-Fshr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757138	F	MP:0010124	decreased bone mineral content	Fshr<tm1(KOMP)Vlcg>/Fshr<tm1(KOMP)Vlcg>	C57BL/6N-Fshr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757138	F	MP:0013279	increased fasting circulating glucose level	Fshr<tm1(KOMP)Vlcg>/Fshr<tm1(KOMP)Vlcg>	C57BL/6N-Fshr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757138	F	MP:0010024	increased total body fat amount	Fshr<tm1(KOMP)Vlcg>/Fshr<tm1(KOMP)Vlcg>	C57BL/6N-Fshr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757138	F	MP:0000063	decreased bone mineral density	Fshr<tm1(KOMP)Vlcg>/Fshr<tm1(KOMP)Vlcg>	C57BL/6N-Fshr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757139	M	MP:0000222	decreased neutrophil cell number	Fstl1<tm1b(EUCOMM)Hmgu>/Fstl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fstl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757139	M	MP:0005013	increased lymphocyte cell number	Fstl1<tm1b(EUCOMM)Hmgu>/Fstl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fstl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757139	F	MP:0005178	increased circulating cholesterol level	Fstl1<tm1b(EUCOMM)Hmgu>/Fstl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fstl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757139	F	MP:0001556	increased circulating HDL cholesterol level	Fstl1<tm1b(EUCOMM)Hmgu>/Fstl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fstl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757139	M	MP:0005293	impaired glucose tolerance	Fstl1<tm1b(EUCOMM)Hmgu>/Fstl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fstl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757140	M	MP:0011965	decreased total retina thickness	Ftsj1<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Ftsj1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757140	M	MP:0003733	abnormal retina inner nuclear layer morphology	Ftsj1<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Ftsj1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757140	M	MP:0002942	decreased circulating alanine transaminase level	Ftsj1<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Ftsj1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757140	M	MP:0005632	decreased circulating aspartate transaminase level	Ftsj1<tm1b(EUCOMM)Wtsi>/Y	C57BL/6N-Ftsj1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757141	F	MP:0001399	hyperactivity	Ftsj1<tm1b(EUCOMM)Wtsi>/Ftsj1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ftsj1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757141	F	MP:0003733	abnormal retina inner nuclear layer morphology	Ftsj1<tm1b(EUCOMM)Wtsi>/Ftsj1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ftsj1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757141	F	MP:0002792	abnormal retina vasculature morphology	Ftsj1<tm1b(EUCOMM)Wtsi>/Ftsj1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ftsj1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757141	F	MP:0011965	decreased total retina thickness	Ftsj1<tm1b(EUCOMM)Wtsi>/Ftsj1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ftsj1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757141	F	MP:0000198	decreased circulating phosphate level	Ftsj1<tm1b(EUCOMM)Wtsi>/Ftsj1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ftsj1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757142	F	MP:0002544	brachydactyly	Furin<tm1b(EUCOMM)Wtsi>/Furin<+>	C57BL/6N-Furin<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5757142	F	MP:0002098	abnormal vibrissa morphology	Furin<tm1b(EUCOMM)Wtsi>/Furin<+>	C57BL/6N-Furin<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5757144	F	MP:0010378	increased respiratory quotient	Fus<tm1.1(KOMP)Vlcg>/Fus<+>	C57BL/6N-Fus<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757146	F	MP:0003179	thrombocytopenia	Fyb1<tm1b(EUCOMM)Hmgu>/Fyb1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fyb1<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757146	M	MP:0010378	increased respiratory quotient	Fyb1<tm1b(EUCOMM)Hmgu>/Fyb1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fyb1<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757146	M	MP:0001303	abnormal lens morphology	Fyb1<tm1b(EUCOMM)Hmgu>/Fyb1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fyb1<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757146	M	MP:0001304	cataract	Fyb1<tm1b(EUCOMM)Hmgu>/Fyb1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fyb1<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757147	F	MP:0010053	decreased grip strength	Fzd3<tm1b(EUCOMM)Hmgu>/Fzd3<+>	C57BL/6N-Fzd3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757147	M	MP:0005293	impaired glucose tolerance	Fzd3<tm1b(EUCOMM)Hmgu>/Fzd3<+>	C57BL/6N-Fzd3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757147	M	MP:0010024	increased total body fat amount	Fzd3<tm1b(EUCOMM)Hmgu>/Fzd3<+>	C57BL/6N-Fzd3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757147	M	MP:0010124	decreased bone mineral content	Fzd3<tm1b(EUCOMM)Hmgu>/Fzd3<+>	C57BL/6N-Fzd3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757149	M	MP:0000220	increased monocyte cell number	Gabarapl2<tm1b(EUCOMM)Hmgu>/Gabarapl2<+>	C57BL/6N-Gabarapl2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757149	M	MP:0002874	decreased hemoglobin content	Gabarapl2<tm1b(EUCOMM)Hmgu>/Gabarapl2<+>	C57BL/6N-Gabarapl2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757149	M	MP:0005419	decreased circulating serum albumin level	Gabarapl2<tm1b(EUCOMM)Hmgu>/Gabarapl2<+>	C57BL/6N-Gabarapl2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757149	M	MP:0000219	increased neutrophil cell number	Gabarapl2<tm1b(EUCOMM)Hmgu>/Gabarapl2<+>	C57BL/6N-Gabarapl2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757149	M	MP:0002833	increased heart weight	Gabarapl2<tm1b(EUCOMM)Hmgu>/Gabarapl2<+>	C57BL/6N-Gabarapl2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757151	M	MP:0005293	impaired glucose tolerance	Gad2<tm1b(EUCOMM)Wtsi>/Gad2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gad2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757151	M	MP:0002968	increased circulating alkaline phosphatase level	Gad2<tm1b(EUCOMM)Wtsi>/Gad2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gad2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757151	M	MP:0002797	increased thigmotaxis	Gad2<tm1b(EUCOMM)Wtsi>/Gad2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gad2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757151	M	MP:0003019	increased circulating chloride level	Gad2<tm1b(EUCOMM)Wtsi>/Gad2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gad2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757151	M	MP:0009142	decreased prepulse inhibition	Gad2<tm1b(EUCOMM)Wtsi>/Gad2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gad2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757151	M	MP:0001402	decreased locomotor activity	Gad2<tm1b(EUCOMM)Wtsi>/Gad2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gad2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757151	F	MP:0005633	increased circulating sodium level	Gad2<tm1b(EUCOMM)Wtsi>/Gad2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gad2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757151	F	MP:0001417	decreased exploration in new environment	Gad2<tm1b(EUCOMM)Wtsi>/Gad2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gad2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757151	M	MP:0004924	abnormal behavior	Gad2<tm1b(EUCOMM)Wtsi>/Gad2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gad2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757151	F	MP:0002574	increased vertical activity	Gad2<tm1b(EUCOMM)Wtsi>/Gad2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gad2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757151	M	MP:0001363	increased anxiety-related response	Gad2<tm1b(EUCOMM)Wtsi>/Gad2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gad2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757153	M	MP:0003960	increased lean body mass	Galnt18<tm1b(KOMP)Wtsi>/Galnt18<tm1b(KOMP)Wtsi>	C57BL/6N-Galnt18<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757153	M	MP:0010025	decreased total body fat amount	Galnt18<tm1b(KOMP)Wtsi>/Galnt18<tm1b(KOMP)Wtsi>	C57BL/6N-Galnt18<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757153	F	MP:0002968	increased circulating alkaline phosphatase level	Galnt18<tm1b(KOMP)Wtsi>/Galnt18<tm1b(KOMP)Wtsi>	C57BL/6N-Galnt18<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757153	M	MP:0010088	decreased circulating fructosamine level	Galnt18<tm1b(KOMP)Wtsi>/Galnt18<tm1b(KOMP)Wtsi>	C57BL/6N-Galnt18<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757153	M	MP:0010067	increased red blood cell distribution width	Galnt18<tm1b(KOMP)Wtsi>/Galnt18<tm1b(KOMP)Wtsi>	C57BL/6N-Galnt18<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757158	F	MP:0001697	abnormal embryo size	Gata2<tm1b(KOMP)Wtsi>/Gata2<+>	C57BL/6N-Gata2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757158	M	MP:0004931	enlarged epididymis	Gata2<tm1b(KOMP)Wtsi>/Gata2<+>	C57BL/6N-Gata2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757158	M	MP:0004727	absent epididymis	Gata2<tm1b(KOMP)Wtsi>/Gata2<+>	C57BL/6N-Gata2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757158	F	MP:0003984	embryonic growth retardation	Gata2<tm1b(KOMP)Wtsi>/Gata2<+>	C57BL/6N-Gata2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757158	M	MP:0002631	abnormal epididymis morphology	Gata2<tm1b(KOMP)Wtsi>/Gata2<+>	C57BL/6N-Gata2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757158	F	MP:0001126	abnormal ovary morphology	Gata2<tm1b(KOMP)Wtsi>/Gata2<+>	C57BL/6N-Gata2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757158	M	MP:0002135	abnormal kidney morphology	Gata2<tm1b(KOMP)Wtsi>/Gata2<+>	C57BL/6N-Gata2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757159	F	MP:0003233	prolonged QT interval	Gatm<tm1b(KOMP)Wtsi>/Gatm<tm1b(KOMP)Wtsi>	C57BL/6N-Gatm<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757159	F	MP:0001926	female infertility	Gatm<tm1b(KOMP)Wtsi>/Gatm<tm1b(KOMP)Wtsi>	C57BL/6N-Gatm<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757159	F	MP:0004156	abnormal QT variability	Gatm<tm1b(KOMP)Wtsi>/Gatm<tm1b(KOMP)Wtsi>	C57BL/6N-Gatm<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757159	F	MP:0005627	increased circulating potassium level	Gatm<tm1b(KOMP)Wtsi>/Gatm<tm1b(KOMP)Wtsi>	C57BL/6N-Gatm<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757159	F	MP:0008806	increased circulating amylase level	Gatm<tm1b(KOMP)Wtsi>/Gatm<tm1b(KOMP)Wtsi>	C57BL/6N-Gatm<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757159	F	MP:0005385	cardiovascular system phenotype	Gatm<tm1b(KOMP)Wtsi>/Gatm<tm1b(KOMP)Wtsi>	C57BL/6N-Gatm<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757159	F	MP:0010570	prolonged ST segment	Gatm<tm1b(KOMP)Wtsi>/Gatm<tm1b(KOMP)Wtsi>	C57BL/6N-Gatm<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757159	M	MP:0003179	thrombocytopenia	Gatm<tm1b(KOMP)Wtsi>/Gatm<tm1b(KOMP)Wtsi>	C57BL/6N-Gatm<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757159	M	MP:0005179	decreased circulating cholesterol level	Gatm<tm1b(KOMP)Wtsi>/Gatm<tm1b(KOMP)Wtsi>	C57BL/6N-Gatm<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757159	M	MP:0005561	increased mean corpuscular hemoglobin	Gatm<tm1b(KOMP)Wtsi>/Gatm<tm1b(KOMP)Wtsi>	C57BL/6N-Gatm<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757159	F	MP:0004122	abnormal sinus arrhythmia	Gatm<tm1b(KOMP)Wtsi>/Gatm<tm1b(KOMP)Wtsi>	C57BL/6N-Gatm<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757159	M	MP:0001925	male infertility	Gatm<tm1b(KOMP)Wtsi>/Gatm<tm1b(KOMP)Wtsi>	C57BL/6N-Gatm<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757160	F	MP:0002968	increased circulating alkaline phosphatase level	Gbx1<tm1b(KOMP)Wtsi>/Gbx1<tm1b(KOMP)Wtsi>	C57BL/6N-Gbx1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757160	F	MP:0001513	limb grasping	Gbx1<tm1b(KOMP)Wtsi>/Gbx1<tm1b(KOMP)Wtsi>	C57BL/6N-Gbx1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757160	M	MP:0011874	enlarged urinary bladder	Gbx1<tm1b(KOMP)Wtsi>/Gbx1<tm1b(KOMP)Wtsi>	C57BL/6N-Gbx1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757163	F	MP:0000689	abnormal spleen morphology	Gdpd5<tm1b(EUCOMM)Hmgu>/Gdpd5<+>	C57BL/6N-Gdpd5<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5757166	M	MP:0001289	persistence of hyaloid vascular system	Gfpt1<tm1b(EUCOMM)Wtsi>/Gfpt1<+>	C57BL/6N-Gfpt1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757168	M	MP:0005419	decreased circulating serum albumin level	Gfpt2<tm1b(EUCOMM)Wtsi>/Gfpt2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gfpt2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757168	M	MP:0010067	increased red blood cell distribution width	Gfpt2<tm1b(EUCOMM)Wtsi>/Gfpt2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gfpt2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757168	F	MP:0002100	abnormal tooth morphology	Gfpt2<tm1b(EUCOMM)Wtsi>/Gfpt2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gfpt2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757168	M	MP:0013279	increased fasting circulating glucose level	Gfpt2<tm1b(EUCOMM)Wtsi>/Gfpt2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gfpt2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757169	F	MP:0005567	decreased circulating total protein level	Ggnbp2<tm1b(KOMP)Wtsi>/Ggnbp2<+>	C57BL/6N-Ggnbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757169	M	MP:0002941	increased circulating alanine transaminase level	Ggnbp2<tm1b(KOMP)Wtsi>/Ggnbp2<+>	C57BL/6N-Ggnbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757169	F	MP:0010393	shortened QRS complex duration	Ggnbp2<tm1b(KOMP)Wtsi>/Ggnbp2<+>	C57BL/6N-Ggnbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757170	F	MP:0001293	anophthalmia	Ggnbp2<tm1b(KOMP)Wtsi>/Ggnbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ggnbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757170	F	MP:0001697	abnormal embryo size	Ggnbp2<tm1b(KOMP)Wtsi>/Ggnbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ggnbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757171	M	MP:0001556	increased circulating HDL cholesterol level	Ggps1<tm1b(EUCOMM)Wtsi>/Ggps1<+>	C57BL/6N-Ggps1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757171	M	MP:0005293	impaired glucose tolerance	Ggps1<tm1b(EUCOMM)Wtsi>/Ggps1<+>	C57BL/6N-Ggps1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757171	F	MP:0001304	cataract	Ggps1<tm1b(EUCOMM)Wtsi>/Ggps1<+>	C57BL/6N-Ggps1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757171	F	MP:0000367	abnormal coat/ hair morphology	Ggps1<tm1b(EUCOMM)Wtsi>/Ggps1<+>	C57BL/6N-Ggps1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757171	F	MP:0001303	abnormal lens morphology	Ggps1<tm1b(EUCOMM)Wtsi>/Ggps1<+>	C57BL/6N-Ggps1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757171	M	MP:0010097	abnormal retina blood vessel morphology	Ggps1<tm1b(EUCOMM)Wtsi>/Ggps1<+>	C57BL/6N-Ggps1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757171	M	MP:0005178	increased circulating cholesterol level	Ggps1<tm1b(EUCOMM)Wtsi>/Ggps1<+>	C57BL/6N-Ggps1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757171	M	MP:0005559	increased circulating glucose level	Ggps1<tm1b(EUCOMM)Wtsi>/Ggps1<+>	C57BL/6N-Ggps1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757171	F	MP:0000218	increased leukocyte cell number	Ggps1<tm1b(EUCOMM)Wtsi>/Ggps1<+>	C57BL/6N-Ggps1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757173	F	MP:0001926	female infertility	Gh<tm1.1(KOMP)Vlcg>/Gh<tm1.1(KOMP)Vlcg>	C57BL/6N-Gh<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757173	M	MP:0003402	decreased liver weight	Gh<tm1.1(KOMP)Vlcg>/Gh<tm1.1(KOMP)Vlcg>	C57BL/6N-Gh<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757173	M	MP:0005631	decreased lung weight	Gh<tm1.1(KOMP)Vlcg>/Gh<tm1.1(KOMP)Vlcg>	C57BL/6N-Gh<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757173	M	MP:0001925	male infertility	Gh<tm1.1(KOMP)Vlcg>/Gh<tm1.1(KOMP)Vlcg>	C57BL/6N-Gh<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757173	F	MP:0003795	abnormal bone structure	Gh<tm1.1(KOMP)Vlcg>/Gh<tm1.1(KOMP)Vlcg>	C57BL/6N-Gh<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757173	M	MP:0002175	decreased brain weight	Gh<tm1.1(KOMP)Vlcg>/Gh<tm1.1(KOMP)Vlcg>	C57BL/6N-Gh<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757173	M	MP:0003179	thrombocytopenia	Gh<tm1.1(KOMP)Vlcg>/Gh<tm1.1(KOMP)Vlcg>	C57BL/6N-Gh<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757173	M	MP:0003918	decreased kidney weight	Gh<tm1.1(KOMP)Vlcg>/Gh<tm1.1(KOMP)Vlcg>	C57BL/6N-Gh<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757173	F	MP:0013278	decreased fasting circulating glucose level	Gh<tm1.1(KOMP)Vlcg>/Gh<tm1.1(KOMP)Vlcg>	C57BL/6N-Gh<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757173	M	MP:0004953	decreased spleen weight	Gh<tm1.1(KOMP)Vlcg>/Gh<tm1.1(KOMP)Vlcg>	C57BL/6N-Gh<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757173	M	MP:0004956	decreased thymus weight	Gh<tm1.1(KOMP)Vlcg>/Gh<tm1.1(KOMP)Vlcg>	C57BL/6N-Gh<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757174	M	MP:0002631	abnormal epididymis morphology	Gipc3<tm1b(KOMP)Wtsi>/Gipc3<tm1b(KOMP)Wtsi>	C57BL/6N-Gipc3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757174	M	MP:0003179	thrombocytopenia	Gipc3<tm1b(KOMP)Wtsi>/Gipc3<tm1b(KOMP)Wtsi>	C57BL/6N-Gipc3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757174	M	MP:0001297	microphthalmia	Gipc3<tm1b(KOMP)Wtsi>/Gipc3<tm1b(KOMP)Wtsi>	C57BL/6N-Gipc3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757174	F	MP:0000955	abnormal spinal cord morphology	Gipc3<tm1b(KOMP)Wtsi>/Gipc3<tm1b(KOMP)Wtsi>	C57BL/6N-Gipc3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757174	M	MP:0002590	increased mean corpuscular volume	Gipc3<tm1b(KOMP)Wtsi>/Gipc3<tm1b(KOMP)Wtsi>	C57BL/6N-Gipc3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757174	M	MP:0005561	increased mean corpuscular hemoglobin	Gipc3<tm1b(KOMP)Wtsi>/Gipc3<tm1b(KOMP)Wtsi>	C57BL/6N-Gipc3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757174	F	MP:0010511	shortened PR interval	Gipc3<tm1b(KOMP)Wtsi>/Gipc3<tm1b(KOMP)Wtsi>	C57BL/6N-Gipc3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757175	M	MP:0003917	increased kidney weight	Gja8<tm1b(EUCOMM)Hmgu>/Gja8<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gja8<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757175	M	MP:0008806	increased circulating amylase level	Gja8<tm1b(EUCOMM)Hmgu>/Gja8<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gja8<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757177	F	MP:0009709	hydrometra	Gkn1<tm1.1(KOMP)Vlcg>/Gkn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757177	F	MP:0000458	abnormal mandible morphology	Gkn1<tm1.1(KOMP)Vlcg>/Gkn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757177	M	MP:0000274	enlarged heart	Gkn1<tm1.1(KOMP)Vlcg>/Gkn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757177	F	MP:0001120	abnormal uterus morphology	Gkn1<tm1.1(KOMP)Vlcg>/Gkn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757177	M	MP:0000266	abnormal heart morphology	Gkn1<tm1.1(KOMP)Vlcg>/Gkn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757177	M	MP:0002135	abnormal kidney morphology	Gkn1<tm1.1(KOMP)Vlcg>/Gkn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757177	F	MP:0000438	abnormal cranium morphology	Gkn1<tm1.1(KOMP)Vlcg>/Gkn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757177	F	MP:0001926	female infertility	Gkn1<tm1.1(KOMP)Vlcg>/Gkn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757178	M	MP:0001488	increased startle reflex	Gm12258<tm1b(EUCOMM)Hmgu>/Gm12258<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gm12258<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757180	F	MP:0001523	impaired righting response	Gnao1<tm1b(EUCOMM)Hmgu>/Gnao1<+>	C57BL/6N-Gnao1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757180	M	MP:0002875	decreased erythrocyte cell number	Gnao1<tm1b(EUCOMM)Hmgu>/Gnao1<+>	C57BL/6N-Gnao1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757180	F	MP:0003795	abnormal bone structure	Gnao1<tm1b(EUCOMM)Hmgu>/Gnao1<+>	C57BL/6N-Gnao1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757180	F	MP:0005012	decreased eosinophil cell number	Gnao1<tm1b(EUCOMM)Hmgu>/Gnao1<+>	C57BL/6N-Gnao1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757180	M	MP:0010379	decreased respiratory quotient	Gnao1<tm1b(EUCOMM)Hmgu>/Gnao1<+>	C57BL/6N-Gnao1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757180	M	MP:0005565	increased blood urea nitrogen level	Gnao1<tm1b(EUCOMM)Hmgu>/Gnao1<+>	C57BL/6N-Gnao1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757180	M	MP:0005561	increased mean corpuscular hemoglobin	Gnao1<tm1b(EUCOMM)Hmgu>/Gnao1<+>	C57BL/6N-Gnao1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757180	M	MP:0008806	increased circulating amylase level	Gnao1<tm1b(EUCOMM)Hmgu>/Gnao1<+>	C57BL/6N-Gnao1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757180	M	MP:0005419	decreased circulating serum albumin level	Gnao1<tm1b(EUCOMM)Hmgu>/Gnao1<+>	C57BL/6N-Gnao1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757180	M	MP:0001552	increased circulating triglyceride level	Gnao1<tm1b(EUCOMM)Hmgu>/Gnao1<+>	C57BL/6N-Gnao1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757180	F	MP:0010068	decreased red blood cell distribution width	Gnao1<tm1b(EUCOMM)Hmgu>/Gnao1<+>	C57BL/6N-Gnao1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757180	F	MP:0010124	decreased bone mineral content	Gnao1<tm1b(EUCOMM)Hmgu>/Gnao1<+>	C57BL/6N-Gnao1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757180	M	MP:0013278	decreased fasting circulating glucose level	Gnao1<tm1b(EUCOMM)Hmgu>/Gnao1<+>	C57BL/6N-Gnao1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757182	M	MP:0005559	increased circulating glucose level	Gng13<tm1.1(KOMP)Vlcg>/Gng13<+>	C57BL/6N-Gng13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757182	M	MP:0010024	increased total body fat amount	Gng13<tm1.1(KOMP)Vlcg>/Gng13<+>	C57BL/6N-Gng13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757183	F	MP:0001120	abnormal uterus morphology	Gng13<tm1.1(KOMP)Vlcg>/Gng13<tm1.1(KOMP)Vlcg>	C57BL/6N-Gng13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757183	F	MP:0002989	small kidney	Gng13<tm1.1(KOMP)Vlcg>/Gng13<tm1.1(KOMP)Vlcg>	C57BL/6N-Gng13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757185	M	MP:0005293	impaired glucose tolerance	Golga3<tm1b(EUCOMM)Hmgu>/Golga3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Golga3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757185	F	MP:0002874	decreased hemoglobin content	Golga3<tm1b(EUCOMM)Hmgu>/Golga3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Golga3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757185	M	MP:0001925	male infertility	Golga3<tm1b(EUCOMM)Hmgu>/Golga3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Golga3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757185	M	MP:0002941	increased circulating alanine transaminase level	Golga3<tm1b(EUCOMM)Hmgu>/Golga3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Golga3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757185	M	MP:0005343	increased circulating aspartate transaminase level	Golga3<tm1b(EUCOMM)Hmgu>/Golga3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Golga3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757186	M	MP:0001406	abnormal gait	Gosr2<tm1b(EUCOMM)Hmgu>/Gosr2<+>	C57BL/6N-Gosr2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757186	M	MP:0010087	increased circulating fructosamine level	Gosr2<tm1b(EUCOMM)Hmgu>/Gosr2<+>	C57BL/6N-Gosr2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757188	M	MP:0002989	small kidney	Gpc2<tm1.1(KOMP)Vlcg>/Gpc2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpc2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757188	M	MP:0002768	small adrenal glands	Gpc2<tm1.1(KOMP)Vlcg>/Gpc2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpc2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757188	F	MP:0004122	abnormal sinus arrhythmia	Gpc2<tm1.1(KOMP)Vlcg>/Gpc2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpc2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757189	F	MP:0006358	absent pinna reflex	Gpr152<tm1b(EUCOMM)Wtsi>/Gpr152<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gpr152<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757191	F	MP:0002590	increased mean corpuscular volume	Gpr182<tm2b(KOMP)Wtsi>/Gpr182<tm2b(KOMP)Wtsi>	C57BL/6N-Gpr182<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757191	M	MP:0000063	decreased bone mineral density	Gpr182<tm2b(KOMP)Wtsi>/Gpr182<tm2b(KOMP)Wtsi>	C57BL/6N-Gpr182<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757191	M	MP:0004952	increased spleen weight	Gpr182<tm2b(KOMP)Wtsi>/Gpr182<tm2b(KOMP)Wtsi>	C57BL/6N-Gpr182<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757191	F	MP:0001399	hyperactivity	Gpr182<tm2b(KOMP)Wtsi>/Gpr182<tm2b(KOMP)Wtsi>	C57BL/6N-Gpr182<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757192	M	MP:0002875	decreased erythrocyte cell number	Gpr22<tm1b(KOMP)Wtsi>/Gpr22<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr22<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757192	M	MP:0005553	increased circulating creatinine level	Gpr22<tm1b(KOMP)Wtsi>/Gpr22<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr22<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757192	M	MP:0001566	increased circulating phosphate level	Gpr22<tm1b(KOMP)Wtsi>/Gpr22<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr22<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757192	M	MP:0000208	decreased hematocrit	Gpr22<tm1b(KOMP)Wtsi>/Gpr22<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr22<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757192	F	MP:0002941	increased circulating alanine transaminase level	Gpr22<tm1b(KOMP)Wtsi>/Gpr22<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr22<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757192	F	MP:0005343	increased circulating aspartate transaminase level	Gpr22<tm1b(KOMP)Wtsi>/Gpr22<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr22<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757192	M	MP:0003960	increased lean body mass	Gpr22<tm1b(KOMP)Wtsi>/Gpr22<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr22<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757192	M	MP:0010025	decreased total body fat amount	Gpr22<tm1b(KOMP)Wtsi>/Gpr22<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr22<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757192	M	MP:0005419	decreased circulating serum albumin level	Gpr22<tm1b(KOMP)Wtsi>/Gpr22<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr22<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757192	F	MP:0005627	increased circulating potassium level	Gpr22<tm1b(KOMP)Wtsi>/Gpr22<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr22<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757192	M	MP:0002874	decreased hemoglobin content	Gpr22<tm1b(KOMP)Wtsi>/Gpr22<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr22<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757192	M	MP:0001406	abnormal gait	Gpr22<tm1b(KOMP)Wtsi>/Gpr22<tm1b(KOMP)Wtsi>	C57BL/6N-Gpr22<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757196	M	MP:0001304	cataract	Gpsm2<tm1b(EUCOMM)Wtsi>/Gpsm2<+>	C57BL/6N-Gpsm2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757196	M	MP:0001303	abnormal lens morphology	Gpsm2<tm1b(EUCOMM)Wtsi>/Gpsm2<+>	C57BL/6N-Gpsm2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757198	M	MP:0005293	impaired glucose tolerance	Gpx3<tm1b(KOMP)Wtsi>/Gpx3<+>	C57BL/6N-Gpx3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757200	F	MP:0001312	abnormal cornea morphology	Grb7<tm1b(EUCOMM)Wtsi>/Grb7<tm1b(EUCOMM)Wtsi>	C57BL/6N-Grb7<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757202	M	MP:0010024	increased total body fat amount	Grm3<tm1b(KOMP)Wtsi>/Grm3<tm1b(KOMP)Wtsi>	C57BL/6N-Grm3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757202	M	MP:0001297	microphthalmia	Grm3<tm1b(KOMP)Wtsi>/Grm3<tm1b(KOMP)Wtsi>	C57BL/6N-Grm3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757202	M	MP:0010124	decreased bone mineral content	Grm3<tm1b(KOMP)Wtsi>/Grm3<tm1b(KOMP)Wtsi>	C57BL/6N-Grm3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757202	M	MP:0005293	impaired glucose tolerance	Grm3<tm1b(KOMP)Wtsi>/Grm3<tm1b(KOMP)Wtsi>	C57BL/6N-Grm3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757202	M	MP:0003961	decreased lean body mass	Grm3<tm1b(KOMP)Wtsi>/Grm3<tm1b(KOMP)Wtsi>	C57BL/6N-Grm3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757203	F	MP:0002833	increased heart weight	Grm6<tm1b(EUCOMM)Wtsi>/Grm6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Grm6<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757203	M	MP:0002092	abnormal eye morphology	Grm6<tm1b(EUCOMM)Wtsi>/Grm6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Grm6<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757203	M	MP:0001304	cataract	Grm6<tm1b(EUCOMM)Wtsi>/Grm6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Grm6<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757204	M	MP:0001157	small seminal vesicle	Grtp1<tm1b(EUCOMM)Hmgu>/Grtp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Grtp1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757204	F	MP:0005343	increased circulating aspartate transaminase level	Grtp1<tm1b(EUCOMM)Hmgu>/Grtp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Grtp1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757204	F	MP:0001297	microphthalmia	Grtp1<tm1b(EUCOMM)Hmgu>/Grtp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Grtp1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757204	F	MP:0002941	increased circulating alanine transaminase level	Grtp1<tm1b(EUCOMM)Hmgu>/Grtp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Grtp1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757205	F	MP:0001417	decreased exploration in new environment	Gsta4<tm1b(EUCOMM)Hmgu>/Gsta4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gsta4<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757205	F	MP:0002075	abnormal coat/hair pigmentation	Gsta4<tm1b(EUCOMM)Hmgu>/Gsta4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gsta4<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757205	F	MP:0002699	abnormal vitreous body morphology	Gsta4<tm1b(EUCOMM)Hmgu>/Gsta4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gsta4<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757205	M	MP:0010067	increased red blood cell distribution width	Gsta4<tm1b(EUCOMM)Hmgu>/Gsta4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gsta4<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757205	F	MP:0001303	abnormal lens morphology	Gsta4<tm1b(EUCOMM)Hmgu>/Gsta4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gsta4<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757205	M	MP:0001325	abnormal retina morphology	Gsta4<tm1b(EUCOMM)Hmgu>/Gsta4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gsta4<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757206	M	MP:0005628	decreased circulating potassium level	Gstcd<tm1b(EUCOMM)Wtsi>/Gstcd<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gstcd<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757206	M	MP:0000691	enlarged spleen	Gstcd<tm1b(EUCOMM)Wtsi>/Gstcd<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gstcd<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757206	M	MP:0005566	decreased blood urea nitrogen level	Gstcd<tm1b(EUCOMM)Wtsi>/Gstcd<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gstcd<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757209	F	MP:0001399	hyperactivity	Gtpbp2<tm1b(KOMP)Mbp>/Gtpbp2<tm1b(KOMP)Mbp>	C57BL/6N-Gtpbp2<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5757209	M	MP:0000702	enlarged lymph nodes	Gtpbp2<tm1b(KOMP)Mbp>/Gtpbp2<tm1b(KOMP)Mbp>	C57BL/6N-Gtpbp2<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5757210	M	MP:0004609	vertebral fusion	Gyg1<tm1b(KOMP)Wtsi>/Gyg1<+>	C57BL/6N-Gyg1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757210	M	MP:0010052	increased grip strength	Gyg1<tm1b(KOMP)Wtsi>/Gyg1<+>	C57BL/6N-Gyg1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757217	F	MP:0010052	increased grip strength	Hectd2<tm1b(KOMP)Wtsi>/Hectd2<tm1b(KOMP)Wtsi>	C57BL/6N-Hectd2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757217	M	MP:0000149	abnormal scapula morphology	Hectd2<tm1b(KOMP)Wtsi>/Hectd2<tm1b(KOMP)Wtsi>	C57BL/6N-Hectd2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757217	M	MP:0002631	abnormal epididymis morphology	Hectd2<tm1b(KOMP)Wtsi>/Hectd2<tm1b(KOMP)Wtsi>	C57BL/6N-Hectd2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757218	F	MP:0010124	decreased bone mineral content	Hectd3<tm1(NCOM)Cmhd>/Hectd3<tm1(NCOM)Cmhd>	C57BL/6N-Hectd3<tm1(NCOM)Cmhd>/Nju	N	MGI:5576271
MGI:5757218	M	MP:0001925	male infertility	Hectd3<tm1(NCOM)Cmhd>/Hectd3<tm1(NCOM)Cmhd>	C57BL/6N-Hectd3<tm1(NCOM)Cmhd>/Nju	N	MGI:5576271
MGI:5757218	F	MP:0003795	abnormal bone structure	Hectd3<tm1(NCOM)Cmhd>/Hectd3<tm1(NCOM)Cmhd>	C57BL/6N-Hectd3<tm1(NCOM)Cmhd>/Nju	N	MGI:5576271
MGI:5757218	F	MP:0010024	increased total body fat amount	Hectd3<tm1(NCOM)Cmhd>/Hectd3<tm1(NCOM)Cmhd>	C57BL/6N-Hectd3<tm1(NCOM)Cmhd>/Nju	N	MGI:5576271
MGI:5757218	F	MP:0001926	female infertility	Hectd3<tm1(NCOM)Cmhd>/Hectd3<tm1(NCOM)Cmhd>	C57BL/6N-Hectd3<tm1(NCOM)Cmhd>/Nju	N	MGI:5576271
MGI:5757218	F	MP:0001258	decreased body length	Hectd3<tm1(NCOM)Cmhd>/Hectd3<tm1(NCOM)Cmhd>	C57BL/6N-Hectd3<tm1(NCOM)Cmhd>/Nju	N	MGI:5576271
MGI:5757218	F	MP:0005599	increased cardiac muscle contractility	Hectd3<tm1(NCOM)Cmhd>/Hectd3<tm1(NCOM)Cmhd>	C57BL/6N-Hectd3<tm1(NCOM)Cmhd>/Nju	N	MGI:5576271
MGI:5757220	F	MP:0002606	increased basophil cell number	Herc4<tm1b(KOMP)Wtsi>/Herc4<tm1b(KOMP)Wtsi>	C57BL/6N-Herc4<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757220	M	MP:0005011	increased eosinophil cell number	Herc4<tm1b(KOMP)Wtsi>/Herc4<tm1b(KOMP)Wtsi>	C57BL/6N-Herc4<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757221	F	MP:0011396	abnormal sleep behavior	Heyl<tm1b(KOMP)Wtsi>/Heyl<tm1b(KOMP)Wtsi>	C57BL/6N-Heyl<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757222	F	MP:0010052	increased grip strength	Hhipl1<tm1b(KOMP)Wtsi>/Hhipl1<tm1b(KOMP)Wtsi>	C57BL/6N-Hhipl1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757222	F	MP:0002989	small kidney	Hhipl1<tm1b(KOMP)Wtsi>/Hhipl1<tm1b(KOMP)Wtsi>	C57BL/6N-Hhipl1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757223	M	MP:0013278	decreased fasting circulating glucose level	Hibadh<tm1b(EUCOMM)Wtsi>/Hibadh<tm1b(EUCOMM)Wtsi>	C57BL/6N-Hibadh<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757224	F	MP:0009142	decreased prepulse inhibition	Hip1r<tm2b(KOMP)Wtsi>/Hip1r<tm2b(KOMP)Wtsi>	C57BL/6N-Hip1r<tm2b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757224	F	MP:0001303	abnormal lens morphology	Hip1r<tm2b(KOMP)Wtsi>/Hip1r<tm2b(KOMP)Wtsi>	C57BL/6N-Hip1r<tm2b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757225	M	MP:0002833	increased heart weight	Hipk2<tm2b(EUCOMM)Hmgu>/Hipk2<+>	C57BL/6N-Hipk2<tm2b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757225	M	MP:0003917	increased kidney weight	Hipk2<tm2b(EUCOMM)Hmgu>/Hipk2<+>	C57BL/6N-Hipk2<tm2b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757226	M	MP:0000455	abnormal maxilla morphology	Hipk2<tm2b(EUCOMM)Hmgu>/Hipk2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Hipk2<tm2b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757226	M	MP:0001303	abnormal lens morphology	Hipk2<tm2b(EUCOMM)Hmgu>/Hipk2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Hipk2<tm2b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757228	M	MP:0005011	increased eosinophil cell number	Hnrnpd<tm1b(KOMP)Wtsi>/Hnrnpd<+>	C57BL/6N-Hnrnpd<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757228	F	MP:0002797	increased thigmotaxis	Hnrnpd<tm1b(KOMP)Wtsi>/Hnrnpd<+>	C57BL/6N-Hnrnpd<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757228	F	MP:0004924	abnormal behavior	Hnrnpd<tm1b(KOMP)Wtsi>/Hnrnpd<+>	C57BL/6N-Hnrnpd<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757229	F	MP:0005419	decreased circulating serum albumin level	Hsd17b1<tm1.1(KOMP)Vlcg>/Hsd17b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757229	M	MP:0001523	impaired righting response	Hsd17b1<tm1.1(KOMP)Vlcg>/Hsd17b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757229	F	MP:0001516	abnormal motor coordination/balance	Hsd17b1<tm1.1(KOMP)Vlcg>/Hsd17b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757229	F	MP:0002591	decreased mean corpuscular volume	Hsd17b1<tm1.1(KOMP)Vlcg>/Hsd17b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757229	M	MP:0000208	decreased hematocrit	Hsd17b1<tm1.1(KOMP)Vlcg>/Hsd17b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757229	M	MP:0003020	decreased circulating chloride level	Hsd17b1<tm1.1(KOMP)Vlcg>/Hsd17b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757229	M	MP:0010123	increased bone mineral content	Hsd17b1<tm1.1(KOMP)Vlcg>/Hsd17b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757229	M	MP:0001325	abnormal retina morphology	Hsd17b1<tm1.1(KOMP)Vlcg>/Hsd17b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757229	M	MP:0002875	decreased erythrocyte cell number	Hsd17b1<tm1.1(KOMP)Vlcg>/Hsd17b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757229	M	MP:0005627	increased circulating potassium level	Hsd17b1<tm1.1(KOMP)Vlcg>/Hsd17b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757229	M	MP:0005560	decreased circulating glucose level	Hsd17b1<tm1.1(KOMP)Vlcg>/Hsd17b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757229	M	MP:0002874	decreased hemoglobin content	Hsd17b1<tm1.1(KOMP)Vlcg>/Hsd17b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757230	F	MP:0011396	abnormal sleep behavior	Hsf1<tm1.1(KOMP)Vlcg>/Hsf1<+>	C57BL/6N-Hsf1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757230	F	MP:0001325	abnormal retina morphology	Hsf1<tm1.1(KOMP)Vlcg>/Hsf1<+>	C57BL/6N-Hsf1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757231	F	MP:0005633	increased circulating sodium level	Hsf2<tm1b(KOMP)Wtsi>/Hsf2<tm1b(KOMP)Wtsi>	C57BL/6N-Hsf2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757231	M	MP:0003870	decreased urine glucose level	Hsf2<tm1b(KOMP)Wtsi>/Hsf2<tm1b(KOMP)Wtsi>	C57BL/6N-Hsf2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757232	F	MP:0000195	decreased circulating calcium level	Hspb1<tm1.1(KOMP)Vlcg>/Hspb1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hspb1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757232	F	MP:0005561	increased mean corpuscular hemoglobin	Hspb1<tm1.1(KOMP)Vlcg>/Hspb1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hspb1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757232	M	MP:0002833	increased heart weight	Hspb1<tm1.1(KOMP)Vlcg>/Hspb1<tm1.1(KOMP)Vlcg>	C57BL/6N-Hspb1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757234	M	MP:0002590	increased mean corpuscular volume	Htr1f<tm1.1(KOMP)Vlcg>/Htr1f<tm1.1(KOMP)Vlcg>	C57BL/6N-Htr1f<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757234	M	MP:0011999	abnormal tail length	Htr1f<tm1.1(KOMP)Vlcg>/Htr1f<tm1.1(KOMP)Vlcg>	C57BL/6N-Htr1f<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757234	M	MP:0005633	increased circulating sodium level	Htr1f<tm1.1(KOMP)Vlcg>/Htr1f<tm1.1(KOMP)Vlcg>	C57BL/6N-Htr1f<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757238	F	MP:0001510	abnormal coat appearance	Hyal3<tm1.1(KOMP)Vlcg>/Hyal3<tm1.1(KOMP)Vlcg>	C57BL/6N-Hyal3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757240	F	MP:0002966	decreased circulating alkaline phosphatase level	Iah1<tm1b(EUCOMM)Hmgu>/Iah1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Iah1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757240	M	MP:0009141	increased prepulse inhibition	Iah1<tm1b(EUCOMM)Hmgu>/Iah1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Iah1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757240	M	MP:0003233	prolonged QT interval	Iah1<tm1b(EUCOMM)Hmgu>/Iah1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Iah1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757240	M	MP:0010570	prolonged ST segment	Iah1<tm1b(EUCOMM)Hmgu>/Iah1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Iah1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757241	F	MP:0011110	preweaning lethality, incomplete penetrance	Idh1<tm1b(EUCOMM)Wtsi>/Idh1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Idh1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757243	F	MP:0000702	enlarged lymph nodes	Ifi44<tm1b(KOMP)Wtsi>/Ifi44<tm1b(KOMP)Wtsi>	C57BL/6N-Ifi44<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757243	M	MP:0005011	increased eosinophil cell number	Ifi44<tm1b(KOMP)Wtsi>/Ifi44<tm1b(KOMP)Wtsi>	C57BL/6N-Ifi44<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757245	M	MP:0003900	shortened QT interval	Igfbp3<tm1b(KOMP)Wtsi>/Igfbp3<tm1b(KOMP)Wtsi>	C57BL/6N-Igfbp3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757245	M	MP:0002764	short tibia	Igfbp3<tm1b(KOMP)Wtsi>/Igfbp3<tm1b(KOMP)Wtsi>	C57BL/6N-Igfbp3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757245	F	MP:0002953	thick ventricular wall	Igfbp3<tm1b(KOMP)Wtsi>/Igfbp3<tm1b(KOMP)Wtsi>	C57BL/6N-Igfbp3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757245	M	MP:0010571	shortened ST segment	Igfbp3<tm1b(KOMP)Wtsi>/Igfbp3<tm1b(KOMP)Wtsi>	C57BL/6N-Igfbp3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757246	F	MP:0011239	abnormal skin coloration	Igfbp7<tm1b(EUCOMM)Hmgu>/Igfbp7<tm1b(EUCOMM)Hmgu>	C57BL/6N-Igfbp7<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5757247	M	MP:0000219	increased neutrophil cell number	Ikzf3<tm1(KOMP)Vlcg>/Ikzf3<tm1(KOMP)Vlcg>	C57BL/6N-Ikzf3<tm1(KOMP)Vlcg>/Rbrc	N	MGI:5576271
MGI:5757247	F	MP:0003179	thrombocytopenia	Ikzf3<tm1(KOMP)Vlcg>/Ikzf3<tm1(KOMP)Vlcg>	C57BL/6N-Ikzf3<tm1(KOMP)Vlcg>/Rbrc	N	MGI:5576271
MGI:5757247	M	MP:0012361	decreased large unstained cell number	Ikzf3<tm1(KOMP)Vlcg>/Ikzf3<tm1(KOMP)Vlcg>	C57BL/6N-Ikzf3<tm1(KOMP)Vlcg>/Rbrc	N	MGI:5576271
MGI:5757248	F	MP:0010052	increased grip strength	Il15<tm1b(EUCOMM)Hmgu>/Il15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il15<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757248	M	MP:0000274	enlarged heart	Il15<tm1b(EUCOMM)Hmgu>/Il15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il15<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757248	M	MP:0005293	impaired glucose tolerance	Il15<tm1b(EUCOMM)Hmgu>/Il15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il15<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757248	F	MP:0001513	limb grasping	Il15<tm1b(EUCOMM)Hmgu>/Il15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il15<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757249	F	MP:0003921	abnormal heart left ventricle morphology	Il17rd<tm1b(EUCOMM)Hmgu>/Il17rd<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il17rd<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757250	M	MP:0000367	abnormal coat/ hair morphology	Il33<tm1.1(KOMP)Vlcg>/Il33<tm1.1(KOMP)Vlcg>	C57BL/6N-Il33<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757250	F	MP:0005333	decreased heart rate	Il33<tm1.1(KOMP)Vlcg>/Il33<tm1.1(KOMP)Vlcg>	C57BL/6N-Il33<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757250	F	MP:0010506	prolonged RR interval	Il33<tm1.1(KOMP)Vlcg>/Il33<tm1.1(KOMP)Vlcg>	C57BL/6N-Il33<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757252	M	MP:0002059	abnormal seminal vesicle morphology	Ino80<tm1a(EUCOMM)Hmgu>/Ino80<+>	C57BL/6N-Ino80<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757252	F	MP:0001529	abnormal vocalization	Ino80<tm1a(EUCOMM)Hmgu>/Ino80<+>	C57BL/6N-Ino80<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757252	M	MP:0001402	decreased locomotor activity	Ino80<tm1a(EUCOMM)Hmgu>/Ino80<+>	C57BL/6N-Ino80<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757252	F	MP:0010392	prolonged QRS complex duration	Ino80<tm1a(EUCOMM)Hmgu>/Ino80<+>	C57BL/6N-Ino80<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757255	M	MP:0010068	decreased red blood cell distribution width	Ints12<tm1b(EUCOMM)Wtsi>/Ints12<+>	C57BL/6N-Ints12<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757255	M	MP:0003961	decreased lean body mass	Ints12<tm1b(EUCOMM)Wtsi>/Ints12<+>	C57BL/6N-Ints12<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757255	M	MP:0001552	increased circulating triglyceride level	Ints12<tm1b(EUCOMM)Wtsi>/Ints12<+>	C57BL/6N-Ints12<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757257	M	MP:0000219	increased neutrophil cell number	Iqce<tm1b(EUCOMM)Hmgu>/Iqce<tm1b(EUCOMM)Hmgu>	C57BL/6N-Iqce<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757257	M	MP:0001392	abnormal locomotor behavior	Iqce<tm1b(EUCOMM)Hmgu>/Iqce<tm1b(EUCOMM)Hmgu>	C57BL/6N-Iqce<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757257	M	MP:0005016	decreased lymphocyte cell number	Iqce<tm1b(EUCOMM)Hmgu>/Iqce<tm1b(EUCOMM)Hmgu>	C57BL/6N-Iqce<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757257	M	MP:0005419	decreased circulating serum albumin level	Iqce<tm1b(EUCOMM)Hmgu>/Iqce<tm1b(EUCOMM)Hmgu>	C57BL/6N-Iqce<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757257	F	MP:0002590	increased mean corpuscular volume	Iqce<tm1b(EUCOMM)Hmgu>/Iqce<tm1b(EUCOMM)Hmgu>	C57BL/6N-Iqce<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757257	M	MP:0000745	tremors	Iqce<tm1b(EUCOMM)Hmgu>/Iqce<tm1b(EUCOMM)Hmgu>	C57BL/6N-Iqce<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757257	F	MP:0002764	short tibia	Iqce<tm1b(EUCOMM)Hmgu>/Iqce<tm1b(EUCOMM)Hmgu>	C57BL/6N-Iqce<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757258	M	MP:0010024	increased total body fat amount	Iqsec3<tm3b(KOMP)Wtsi>/Iqsec3<tm3b(KOMP)Wtsi>	C57BL/6N-Iqsec3<tm3b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757258	M	MP:0000063	decreased bone mineral density	Iqsec3<tm3b(KOMP)Wtsi>/Iqsec3<tm3b(KOMP)Wtsi>	C57BL/6N-Iqsec3<tm3b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757258	M	MP:0010124	decreased bone mineral content	Iqsec3<tm3b(KOMP)Wtsi>/Iqsec3<tm3b(KOMP)Wtsi>	C57BL/6N-Iqsec3<tm3b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757258	M	MP:0005293	impaired glucose tolerance	Iqsec3<tm3b(KOMP)Wtsi>/Iqsec3<tm3b(KOMP)Wtsi>	C57BL/6N-Iqsec3<tm3b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757258	F	MP:0001402	decreased locomotor activity	Iqsec3<tm3b(KOMP)Wtsi>/Iqsec3<tm3b(KOMP)Wtsi>	C57BL/6N-Iqsec3<tm3b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757258	M	MP:0003961	decreased lean body mass	Iqsec3<tm3b(KOMP)Wtsi>/Iqsec3<tm3b(KOMP)Wtsi>	C57BL/6N-Iqsec3<tm3b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757258	M	MP:0013279	increased fasting circulating glucose level	Iqsec3<tm3b(KOMP)Wtsi>/Iqsec3<tm3b(KOMP)Wtsi>	C57BL/6N-Iqsec3<tm3b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757258	F	MP:0020870	decreased thigmotaxis	Iqsec3<tm3b(KOMP)Wtsi>/Iqsec3<tm3b(KOMP)Wtsi>	C57BL/6N-Iqsec3<tm3b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757258	F	MP:0003733	abnormal retina inner nuclear layer morphology	Iqsec3<tm3b(KOMP)Wtsi>/Iqsec3<tm3b(KOMP)Wtsi>	C57BL/6N-Iqsec3<tm3b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757258	F	MP:0011965	decreased total retina thickness	Iqsec3<tm3b(KOMP)Wtsi>/Iqsec3<tm3b(KOMP)Wtsi>	C57BL/6N-Iqsec3<tm3b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757258	M	MP:0001258	decreased body length	Iqsec3<tm3b(KOMP)Wtsi>/Iqsec3<tm3b(KOMP)Wtsi>	C57BL/6N-Iqsec3<tm3b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757260	M	MP:0000745	tremors	Itga2<tm1b(EUCOMM)Hmgu>/Itga2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itga2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757261	M	MP:0000221	decreased leukocyte cell number	Itgae<tm1b(EUCOMM)Wtsi>/Itgae<tm1b(EUCOMM)Wtsi>	C57BL/6N-Itgae<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757261	M	MP:0003961	decreased lean body mass	Itgae<tm1b(EUCOMM)Wtsi>/Itgae<tm1b(EUCOMM)Wtsi>	C57BL/6N-Itgae<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757261	M	MP:0000223	decreased monocyte cell number	Itgae<tm1b(EUCOMM)Wtsi>/Itgae<tm1b(EUCOMM)Wtsi>	C57BL/6N-Itgae<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757261	M	MP:0012361	decreased large unstained cell number	Itgae<tm1b(EUCOMM)Wtsi>/Itgae<tm1b(EUCOMM)Wtsi>	C57BL/6N-Itgae<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757261	M	MP:0005016	decreased lymphocyte cell number	Itgae<tm1b(EUCOMM)Wtsi>/Itgae<tm1b(EUCOMM)Wtsi>	C57BL/6N-Itgae<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757261	M	MP:0000222	decreased neutrophil cell number	Itgae<tm1b(EUCOMM)Wtsi>/Itgae<tm1b(EUCOMM)Wtsi>	C57BL/6N-Itgae<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757263	M	MP:0005562	decreased mean corpuscular hemoglobin	Ivd<tm1b(EUCOMM)Hmgu>/Ivd<+>	C57BL/6N-Ivd<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757263	F	MP:0001303	abnormal lens morphology	Ivd<tm1b(EUCOMM)Hmgu>/Ivd<+>	C57BL/6N-Ivd<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757265	F	MP:0001926	female infertility	Izumo1r<tm1b(KOMP)Wtsi>/Izumo1r<tm1b(KOMP)Wtsi>	C57BL/6N-Izumo1r<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757267	F	MP:0005627	increased circulating potassium level	Jam2<tm1.1(KOMP)Mbp>/Jam2<tm1.1(KOMP)Mbp>	C57BL/6N-Jam2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757267	M	MP:0005633	increased circulating sodium level	Jam2<tm1.1(KOMP)Mbp>/Jam2<tm1.1(KOMP)Mbp>	C57BL/6N-Jam2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757269	M	MP:0005564	increased hemoglobin content	Jup<tm1.1(KOMP)Vlcg>/Jup<+>	C57BL/6N-Jup<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757269	M	MP:0001523	impaired righting response	Jup<tm1.1(KOMP)Vlcg>/Jup<+>	C57BL/6N-Jup<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757269	M	MP:0003064	decreased coping response	Jup<tm1.1(KOMP)Vlcg>/Jup<+>	C57BL/6N-Jup<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757269	M	MP:0000198	decreased circulating phosphate level	Jup<tm1.1(KOMP)Vlcg>/Jup<+>	C57BL/6N-Jup<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757269	F	MP:0013278	decreased fasting circulating glucose level	Jup<tm1.1(KOMP)Vlcg>/Jup<+>	C57BL/6N-Jup<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757273	F	MP:0005561	increased mean corpuscular hemoglobin	Kcnb1<tm1b(EUCOMM)Hmgu>/Kcnb1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcnb1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757273	F	MP:0003960	increased lean body mass	Kcnb1<tm1b(EUCOMM)Hmgu>/Kcnb1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcnb1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757273	F	MP:0001406	abnormal gait	Kcnb1<tm1b(EUCOMM)Hmgu>/Kcnb1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcnb1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757273	M	MP:0001415	increased exploration in new environment	Kcnb1<tm1b(EUCOMM)Hmgu>/Kcnb1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcnb1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757273	F	MP:0002590	increased mean corpuscular volume	Kcnb1<tm1b(EUCOMM)Hmgu>/Kcnb1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcnb1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757275	F	MP:0002966	decreased circulating alkaline phosphatase level	Kctd15<tm1b(EUCOMM)Wtsi>/Kctd15<+>	C57BL/6N-Kctd15<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5757278	F	MP:0000692	small spleen	Kdm1a<tm1(NCOM)Mfgc>/Kdm1a<+>	C57BL/6N-Kdm1a<tm1(NCOM)Mfgc>/Nju	N	MGI:5576271
MGI:5757278	F	MP:0002188	small heart	Kdm1a<tm1(NCOM)Mfgc>/Kdm1a<+>	C57BL/6N-Kdm1a<tm1(NCOM)Mfgc>/Nju	N	MGI:5576271
MGI:5757278	F	MP:0003641	small lung	Kdm1a<tm1(NCOM)Mfgc>/Kdm1a<+>	C57BL/6N-Kdm1a<tm1(NCOM)Mfgc>/Nju	N	MGI:5576271
MGI:5757278	M	MP:0002599	increased mean platelet volume	Kdm1a<tm1(NCOM)Mfgc>/Kdm1a<+>	C57BL/6N-Kdm1a<tm1(NCOM)Mfgc>/Nju	N	MGI:5576271
MGI:5757278	F	MP:0000601	small liver	Kdm1a<tm1(NCOM)Mfgc>/Kdm1a<+>	C57BL/6N-Kdm1a<tm1(NCOM)Mfgc>/Nju	N	MGI:5576271
MGI:5757278	F	MP:0002989	small kidney	Kdm1a<tm1(NCOM)Mfgc>/Kdm1a<+>	C57BL/6N-Kdm1a<tm1(NCOM)Mfgc>/Nju	N	MGI:5576271
MGI:5757281	F	MP:0002968	increased circulating alkaline phosphatase level	Khdrbs3<tm1b(EUCOMM)Hmgu>/Khdrbs3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Khdrbs3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757282	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Kif20a<tm1b(EUCOMM)Hmgu>/Kif20a<+>	C57BL/6N-Kif20a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757284	M	MP:0010123	increased bone mineral content	Kif3b<tm1b(EUCOMM)Wtsi>/Kif3b<+>	C57BL/6N-Kif3b<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757284	F	MP:0010052	increased grip strength	Kif3b<tm1b(EUCOMM)Wtsi>/Kif3b<+>	C57BL/6N-Kif3b<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757287	F	MP:0001523	impaired righting response	Klf7<tm1b(EUCOMM)Hmgu>/Klf7<+>	C57BL/6N-Klf7<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757287	M	MP:0002599	increased mean platelet volume	Klf7<tm1b(EUCOMM)Hmgu>/Klf7<+>	C57BL/6N-Klf7<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757287	M	MP:0000137	abnormal vertebrae morphology	Klf7<tm1b(EUCOMM)Hmgu>/Klf7<+>	C57BL/6N-Klf7<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757287	M	MP:0005419	decreased circulating serum albumin level	Klf7<tm1b(EUCOMM)Hmgu>/Klf7<+>	C57BL/6N-Klf7<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757287	M	MP:0001289	persistence of hyaloid vascular system	Klf7<tm1b(EUCOMM)Hmgu>/Klf7<+>	C57BL/6N-Klf7<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757287	M	MP:0005343	increased circulating aspartate transaminase level	Klf7<tm1b(EUCOMM)Hmgu>/Klf7<+>	C57BL/6N-Klf7<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757289	F	MP:0010024	increased total body fat amount	Klhdc2<tm1b(EUCOMM)Hmgu>/Klhdc2<+>	C57BL/6N-Klhdc2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757289	M	MP:0005016	decreased lymphocyte cell number	Klhdc2<tm1b(EUCOMM)Hmgu>/Klhdc2<+>	C57BL/6N-Klhdc2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757289	F	MP:0000443	abnormal snout morphology	Klhdc2<tm1b(EUCOMM)Hmgu>/Klhdc2<+>	C57BL/6N-Klhdc2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757289	F	MP:0005553	increased circulating creatinine level	Klhdc2<tm1b(EUCOMM)Hmgu>/Klhdc2<+>	C57BL/6N-Klhdc2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757289	M	MP:0002060	abnormal skin morphology	Klhdc2<tm1b(EUCOMM)Hmgu>/Klhdc2<+>	C57BL/6N-Klhdc2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757289	M	MP:0000219	increased neutrophil cell number	Klhdc2<tm1b(EUCOMM)Hmgu>/Klhdc2<+>	C57BL/6N-Klhdc2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757289	F	MP:0000432	abnormal head morphology	Klhdc2<tm1b(EUCOMM)Hmgu>/Klhdc2<+>	C57BL/6N-Klhdc2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757291	M	MP:0012362	increased large unstained cell number	Klhl29<tm1b(EUCOMM)Hmgu>/Klhl29<+>	C57BL/6N-Klhl29<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757291	F	MP:0010570	prolonged ST segment	Klhl29<tm1b(EUCOMM)Hmgu>/Klhl29<+>	C57BL/6N-Klhl29<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757291	F	MP:0003233	prolonged QT interval	Klhl29<tm1b(EUCOMM)Hmgu>/Klhl29<+>	C57BL/6N-Klhl29<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757292	M	MP:0002626	increased heart rate	Klhl29<tm1b(EUCOMM)Hmgu>/Klhl29<tm1b(EUCOMM)Hmgu>	C57BL/6N-Klhl29<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757292	M	MP:0005599	increased cardiac muscle contractility	Klhl29<tm1b(EUCOMM)Hmgu>/Klhl29<tm1b(EUCOMM)Hmgu>	C57BL/6N-Klhl29<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757292	M	MP:0010379	decreased respiratory quotient	Klhl29<tm1b(EUCOMM)Hmgu>/Klhl29<tm1b(EUCOMM)Hmgu>	C57BL/6N-Klhl29<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757294	F	MP:0004952	increased spleen weight	Knop1<tm1b(EUCOMM)Wtsi>/Knop1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Knop1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757294	F	MP:0003019	increased circulating chloride level	Knop1<tm1b(EUCOMM)Wtsi>/Knop1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Knop1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757294	M	MP:0000745	tremors	Knop1<tm1b(EUCOMM)Wtsi>/Knop1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Knop1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757295	M	MP:0002059	abnormal seminal vesicle morphology	Knstrn<tm1b(KOMP)Wtsi>/Knstrn<tm1b(KOMP)Wtsi>	C57BL/6N-Knstrn<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757295	M	MP:0013279	increased fasting circulating glucose level	Knstrn<tm1b(KOMP)Wtsi>/Knstrn<tm1b(KOMP)Wtsi>	C57BL/6N-Knstrn<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757295	M	MP:0000745	tremors	Knstrn<tm1b(KOMP)Wtsi>/Knstrn<tm1b(KOMP)Wtsi>	C57BL/6N-Knstrn<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757295	M	MP:0000208	decreased hematocrit	Knstrn<tm1b(KOMP)Wtsi>/Knstrn<tm1b(KOMP)Wtsi>	C57BL/6N-Knstrn<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757296	M	MP:0008528	polycystic kidney	Krt2<tm1b(KOMP)Wtsi>/Krt2<tm1b(KOMP)Wtsi>	C57BL/6N-Krt2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757296	M	MP:0002135	abnormal kidney morphology	Krt2<tm1b(KOMP)Wtsi>/Krt2<tm1b(KOMP)Wtsi>	C57BL/6N-Krt2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757296	M	MP:0003068	enlarged kidney	Krt2<tm1b(KOMP)Wtsi>/Krt2<tm1b(KOMP)Wtsi>	C57BL/6N-Krt2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757297	F	MP:0000195	decreased circulating calcium level	Krt7<tm1b(KOMP)Wtsi>/Krt7<tm1b(KOMP)Wtsi>	C57BL/6N-Krt7<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757298	F	MP:0005292	improved glucose tolerance	Krt8<tm1b(EUCOMM)Hmgu>/Krt8<+>	C57BL/6N-Krt8<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757298	M	MP:0001417	decreased exploration in new environment	Krt8<tm1b(EUCOMM)Hmgu>/Krt8<+>	C57BL/6N-Krt8<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757298	F	MP:0009141	increased prepulse inhibition	Krt8<tm1b(EUCOMM)Hmgu>/Krt8<+>	C57BL/6N-Krt8<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757298	M	MP:0000219	increased neutrophil cell number	Krt8<tm1b(EUCOMM)Hmgu>/Krt8<+>	C57BL/6N-Krt8<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757300	M	MP:0000266	abnormal heart morphology	Krtap17-1<tm1.1(KOMP)Vlcg>/Krtap17-1<tm1.1(KOMP)Vlcg>	C57BL/6N-Krtap17-1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757300	F	MP:0000063	decreased bone mineral density	Krtap17-1<tm1.1(KOMP)Vlcg>/Krtap17-1<tm1.1(KOMP)Vlcg>	C57BL/6N-Krtap17-1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757300	F	MP:0001258	decreased body length	Krtap17-1<tm1.1(KOMP)Vlcg>/Krtap17-1<tm1.1(KOMP)Vlcg>	C57BL/6N-Krtap17-1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757300	M	MP:0001192	scaly skin	Krtap17-1<tm1.1(KOMP)Vlcg>/Krtap17-1<tm1.1(KOMP)Vlcg>	C57BL/6N-Krtap17-1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757300	M	MP:0005179	decreased circulating cholesterol level	Krtap17-1<tm1.1(KOMP)Vlcg>/Krtap17-1<tm1.1(KOMP)Vlcg>	C57BL/6N-Krtap17-1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757300	M	MP:0001200	thick skin	Krtap17-1<tm1.1(KOMP)Vlcg>/Krtap17-1<tm1.1(KOMP)Vlcg>	C57BL/6N-Krtap17-1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757300	M	MP:0003917	increased kidney weight	Krtap17-1<tm1.1(KOMP)Vlcg>/Krtap17-1<tm1.1(KOMP)Vlcg>	C57BL/6N-Krtap17-1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757300	M	MP:0000274	enlarged heart	Krtap17-1<tm1.1(KOMP)Vlcg>/Krtap17-1<tm1.1(KOMP)Vlcg>	C57BL/6N-Krtap17-1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757301	F	MP:0000274	enlarged heart	Lama5<tm1b(KOMP)Wtsi>/Lama5<+>	C57BL/6N-Lama5<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757303	M	MP:0002060	abnormal skin morphology	Lamb3<tm1b(KOMP)Wtsi>/Lamb3<tm1b(KOMP)Wtsi>	C57BL/6N-Lamb3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757304	M	MP:0013279	increased fasting circulating glucose level	Laptm4a<tm1b(EUCOMM)Hmgu>/Laptm4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Laptm4a<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757304	F	MP:0002764	short tibia	Laptm4a<tm1b(EUCOMM)Hmgu>/Laptm4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Laptm4a<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757304	M	MP:0011965	decreased total retina thickness	Laptm4a<tm1b(EUCOMM)Hmgu>/Laptm4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Laptm4a<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757304	M	MP:0010570	prolonged ST segment	Laptm4a<tm1b(EUCOMM)Hmgu>/Laptm4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Laptm4a<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757305	F	MP:0004952	increased spleen weight	Lbp<tm1b(EUCOMM)Hmgu>/Lbp<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lbp<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757305	M	MP:0010087	increased circulating fructosamine level	Lbp<tm1b(EUCOMM)Hmgu>/Lbp<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lbp<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757305	M	MP:0013279	increased fasting circulating glucose level	Lbp<tm1b(EUCOMM)Hmgu>/Lbp<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lbp<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757306	M	MP:0010024	increased total body fat amount	Lce1f<tm1b(KOMP)Wtsi>/Lce1f<tm1b(KOMP)Wtsi>	C57BL/6N-Lce1f<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757308	M	MP:0006358	absent pinna reflex	Ldhb<tm1b(KOMP)Wtsi>/Ldhb<tm1b(KOMP)Wtsi>	C57BL/6N-Ldhb<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757309	F	MP:0003921	abnormal heart left ventricle morphology	Leprotl1<tm1b(EUCOMM)Hmgu>/Leprotl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Leprotl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757309	M	MP:0002941	increased circulating alanine transaminase level	Leprotl1<tm1b(EUCOMM)Hmgu>/Leprotl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Leprotl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757309	M	MP:0001364	decreased anxiety-related response	Leprotl1<tm1b(EUCOMM)Hmgu>/Leprotl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Leprotl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757309	M	MP:0004924	abnormal behavior	Leprotl1<tm1b(EUCOMM)Hmgu>/Leprotl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Leprotl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757309	F	MP:0002968	increased circulating alkaline phosphatase level	Leprotl1<tm1b(EUCOMM)Hmgu>/Leprotl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Leprotl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757309	F	MP:0002626	increased heart rate	Leprotl1<tm1b(EUCOMM)Hmgu>/Leprotl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Leprotl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757309	M	MP:0001566	increased circulating phosphate level	Leprotl1<tm1b(EUCOMM)Hmgu>/Leprotl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Leprotl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757309	F	MP:0002953	thick ventricular wall	Leprotl1<tm1b(EUCOMM)Hmgu>/Leprotl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Leprotl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757309	F	MP:0005599	increased cardiac muscle contractility	Leprotl1<tm1b(EUCOMM)Hmgu>/Leprotl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Leprotl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757310	M	MP:0003179	thrombocytopenia	Lhcgr<tm1(KOMP)Vlcg>/Lhcgr<tm1(KOMP)Vlcg>	C57BL/6N-Lhcgr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757310	M	MP:0000774	decreased brain size	Lhcgr<tm1(KOMP)Vlcg>/Lhcgr<tm1(KOMP)Vlcg>	C57BL/6N-Lhcgr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757310	M	MP:0000218	increased leukocyte cell number	Lhcgr<tm1(KOMP)Vlcg>/Lhcgr<tm1(KOMP)Vlcg>	C57BL/6N-Lhcgr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757310	M	MP:0000692	small spleen	Lhcgr<tm1(KOMP)Vlcg>/Lhcgr<tm1(KOMP)Vlcg>	C57BL/6N-Lhcgr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757310	M	MP:0000706	small thymus	Lhcgr<tm1(KOMP)Vlcg>/Lhcgr<tm1(KOMP)Vlcg>	C57BL/6N-Lhcgr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757310	M	MP:0002691	small stomach	Lhcgr<tm1(KOMP)Vlcg>/Lhcgr<tm1(KOMP)Vlcg>	C57BL/6N-Lhcgr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757310	M	MP:0002188	small heart	Lhcgr<tm1(KOMP)Vlcg>/Lhcgr<tm1(KOMP)Vlcg>	C57BL/6N-Lhcgr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757310	F	MP:0002591	decreased mean corpuscular volume	Lhcgr<tm1(KOMP)Vlcg>/Lhcgr<tm1(KOMP)Vlcg>	C57BL/6N-Lhcgr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757310	M	MP:0003641	small lung	Lhcgr<tm1(KOMP)Vlcg>/Lhcgr<tm1(KOMP)Vlcg>	C57BL/6N-Lhcgr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757310	M	MP:0000601	small liver	Lhcgr<tm1(KOMP)Vlcg>/Lhcgr<tm1(KOMP)Vlcg>	C57BL/6N-Lhcgr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757310	F	MP:0005013	increased lymphocyte cell number	Lhcgr<tm1(KOMP)Vlcg>/Lhcgr<tm1(KOMP)Vlcg>	C57BL/6N-Lhcgr<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757311	M	MP:0002152	abnormal brain morphology	Lifr<tm1b(EUCOMM)Hmgu>/Lifr<+>	C57BL/6N-Lifr<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757311	F	MP:0001417	decreased exploration in new environment	Lifr<tm1b(EUCOMM)Hmgu>/Lifr<+>	C57BL/6N-Lifr<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757313	F	MP:0020870	decreased thigmotaxis	Lima1<tm1b(KOMP)Wtsi>/Lima1<tm1b(KOMP)Wtsi>	C57BL/6N-Lima1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757315	M	MP:0005292	improved glucose tolerance	Lmna<tm1b(EUCOMM)Wtsi>/Lmna<+>	C57BL/6N-Lmna<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757317	F	MP:0004924	abnormal behavior	Lpar6<tm1.1(KOMP)Vlcg>/Lpar6<tm1.1(KOMP)Vlcg>	C57BL/6N-Lpar6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757317	F	MP:0020870	decreased thigmotaxis	Lpar6<tm1.1(KOMP)Vlcg>/Lpar6<tm1.1(KOMP)Vlcg>	C57BL/6N-Lpar6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757317	M	MP:0002941	increased circulating alanine transaminase level	Lpar6<tm1.1(KOMP)Vlcg>/Lpar6<tm1.1(KOMP)Vlcg>	C57BL/6N-Lpar6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757317	F	MP:0001399	hyperactivity	Lpar6<tm1.1(KOMP)Vlcg>/Lpar6<tm1.1(KOMP)Vlcg>	C57BL/6N-Lpar6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757318	F	MP:0009709	hydrometra	Lpin2<tm1b(KOMP)Wtsi>/Lpin2<tm1b(KOMP)Wtsi>	C57BL/6N-Lpin2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757318	M	MP:0010067	increased red blood cell distribution width	Lpin2<tm1b(KOMP)Wtsi>/Lpin2<tm1b(KOMP)Wtsi>	C57BL/6N-Lpin2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757318	F	MP:0000702	enlarged lymph nodes	Lpin2<tm1b(KOMP)Wtsi>/Lpin2<tm1b(KOMP)Wtsi>	C57BL/6N-Lpin2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757318	F	MP:0009142	decreased prepulse inhibition	Lpin2<tm1b(KOMP)Wtsi>/Lpin2<tm1b(KOMP)Wtsi>	C57BL/6N-Lpin2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757318	F	MP:0002874	decreased hemoglobin content	Lpin2<tm1b(KOMP)Wtsi>/Lpin2<tm1b(KOMP)Wtsi>	C57BL/6N-Lpin2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757319	M	MP:0005012	decreased eosinophil cell number	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0000221	decreased leukocyte cell number	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0002932	abnormal joint morphology	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0008810	increased circulating iron level	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0001392	abnormal locomotor behavior	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0000137	abnormal vertebrae morphology	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0005178	increased circulating cholesterol level	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0000443	abnormal snout morphology	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0005108	abnormal ulna morphology	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0000458	abnormal mandible morphology	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0004509	abnormal pelvic girdle bone morphology	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0001556	increased circulating HDL cholesterol level	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0005016	decreased lymphocyte cell number	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0001566	increased circulating phosphate level	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	F	MP:0003961	decreased lean body mass	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	F	MP:0002966	decreased circulating alkaline phosphatase level	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757319	M	MP:0000552	abnormal radius morphology	Lrrk1<tm1b(KOMP)Wtsi>/Lrrk1<tm1b(KOMP)Wtsi>	C57BL/6N-Lrrk1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757321	M	MP:0010052	increased grip strength	Lsm1<tm1b(EUCOMM)Hmgu>/Lsm1<+>	C57BL/6N-Lsm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757321	M	MP:0003928	increased heart rate variability	Lsm1<tm1b(EUCOMM)Hmgu>/Lsm1<+>	C57BL/6N-Lsm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757321	F	MP:0005633	increased circulating sodium level	Lsm1<tm1b(EUCOMM)Hmgu>/Lsm1<+>	C57BL/6N-Lsm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757322	M	MP:0010506	prolonged RR interval	Lsm1<tm1b(EUCOMM)Hmgu>/Lsm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lsm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757322	F	MP:0010574	dilated aorta	Lsm1<tm1b(EUCOMM)Hmgu>/Lsm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lsm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757322	M	MP:0010053	decreased grip strength	Lsm1<tm1b(EUCOMM)Hmgu>/Lsm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lsm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757322	M	MP:0003928	increased heart rate variability	Lsm1<tm1b(EUCOMM)Hmgu>/Lsm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lsm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757322	M	MP:0001303	abnormal lens morphology	Lsm1<tm1b(EUCOMM)Hmgu>/Lsm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lsm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757322	F	MP:0002968	increased circulating alkaline phosphatase level	Lsm1<tm1b(EUCOMM)Hmgu>/Lsm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lsm1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757325	M	MP:0001146	abnormal testis morphology	Lst1<tm1.1(KOMP)Vlcg>/Lst1<tm1.1(KOMP)Vlcg>	C57BL/6N-Lst1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757325	M	MP:0003960	increased lean body mass	Lst1<tm1.1(KOMP)Vlcg>/Lst1<tm1.1(KOMP)Vlcg>	C57BL/6N-Lst1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757325	M	MP:0010025	decreased total body fat amount	Lst1<tm1.1(KOMP)Vlcg>/Lst1<tm1.1(KOMP)Vlcg>	C57BL/6N-Lst1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757325	M	MP:0000274	enlarged heart	Lst1<tm1.1(KOMP)Vlcg>/Lst1<tm1.1(KOMP)Vlcg>	C57BL/6N-Lst1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757325	M	MP:0001147	small testis	Lst1<tm1.1(KOMP)Vlcg>/Lst1<tm1.1(KOMP)Vlcg>	C57BL/6N-Lst1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757325	M	MP:0001552	increased circulating triglyceride level	Lst1<tm1.1(KOMP)Vlcg>/Lst1<tm1.1(KOMP)Vlcg>	C57BL/6N-Lst1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757325	M	MP:0000266	abnormal heart morphology	Lst1<tm1.1(KOMP)Vlcg>/Lst1<tm1.1(KOMP)Vlcg>	C57BL/6N-Lst1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757327	M	MP:0002590	increased mean corpuscular volume	Lyst<tm1b(EUCOMM)Wtsi>/Lyst<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lyst<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757327	F	MP:0001402	decreased locomotor activity	Lyst<tm1b(EUCOMM)Wtsi>/Lyst<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lyst<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757327	M	MP:0005561	increased mean corpuscular hemoglobin	Lyst<tm1b(EUCOMM)Wtsi>/Lyst<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lyst<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757328	M	MP:0001510	abnormal coat appearance	Maea<tm1b(EUCOMM)Wtsi>/Maea<+>	C57BL/6N-Maea<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757330	F	MP:0000947	convulsive seizures	Mag<tm1.1(KOMP)Vlcg>/Mag<tm1.1(KOMP)Vlcg>	C57BL/6N-Mag<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757330	F	MP:0003064	decreased coping response	Mag<tm1.1(KOMP)Vlcg>/Mag<tm1.1(KOMP)Vlcg>	C57BL/6N-Mag<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757330	M	MP:0010052	increased grip strength	Mag<tm1.1(KOMP)Vlcg>/Mag<tm1.1(KOMP)Vlcg>	C57BL/6N-Mag<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757330	M	MP:0001489	decreased startle reflex	Mag<tm1.1(KOMP)Vlcg>/Mag<tm1.1(KOMP)Vlcg>	C57BL/6N-Mag<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757330	F	MP:0011396	abnormal sleep behavior	Mag<tm1.1(KOMP)Vlcg>/Mag<tm1.1(KOMP)Vlcg>	C57BL/6N-Mag<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757332	M	MP:0002768	small adrenal glands	Man2b2<tm1b(KOMP)Wtsi>/Man2b2<tm1b(KOMP)Wtsi>	C57BL/6N-Man2b2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757332	M	MP:0000702	enlarged lymph nodes	Man2b2<tm1b(KOMP)Wtsi>/Man2b2<tm1b(KOMP)Wtsi>	C57BL/6N-Man2b2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757332	M	MP:0005016	decreased lymphocyte cell number	Man2b2<tm1b(KOMP)Wtsi>/Man2b2<tm1b(KOMP)Wtsi>	C57BL/6N-Man2b2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757332	M	MP:0000219	increased neutrophil cell number	Man2b2<tm1b(KOMP)Wtsi>/Man2b2<tm1b(KOMP)Wtsi>	C57BL/6N-Man2b2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757332	F	MP:0005011	increased eosinophil cell number	Man2b2<tm1b(KOMP)Wtsi>/Man2b2<tm1b(KOMP)Wtsi>	C57BL/6N-Man2b2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757332	F	MP:0001120	abnormal uterus morphology	Man2b2<tm1b(KOMP)Wtsi>/Man2b2<tm1b(KOMP)Wtsi>	C57BL/6N-Man2b2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757332	F	MP:0011110	preweaning lethality, incomplete penetrance	Man2b2<tm1b(KOMP)Wtsi>/Man2b2<tm1b(KOMP)Wtsi>	C57BL/6N-Man2b2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757333	M	MP:0001556	increased circulating HDL cholesterol level	Map3k10<tm1b(EUCOMM)Hmgu>/Map3k10<tm1b(EUCOMM)Hmgu>	C57BL/6N-Map3k10<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757333	M	MP:0005178	increased circulating cholesterol level	Map3k10<tm1b(EUCOMM)Hmgu>/Map3k10<tm1b(EUCOMM)Hmgu>	C57BL/6N-Map3k10<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757334	M	MP:0002968	increased circulating alkaline phosphatase level	Map3k7<tm1b(EUCOMM)Wtsi>/Map3k7<+>	C57BL/6N-Map3k7<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757334	F	MP:0001303	abnormal lens morphology	Map3k7<tm1b(EUCOMM)Wtsi>/Map3k7<+>	C57BL/6N-Map3k7<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757336	M	MP:0011965	decreased total retina thickness	Mapkap1<tm1a(EUCOMM)Wtsi>/Mapkap1<+>	C57BL/6N-Mapkap1<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757336	M	MP:0011962	increased cornea thickness	Mapkap1<tm1a(EUCOMM)Wtsi>/Mapkap1<+>	C57BL/6N-Mapkap1<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757338	F	MP:0002753	dilated heart left ventricle	Mapkap1<tm1b(EUCOMM)Wtsi>/Mapkap1<+>	C57BL/6N-Mapkap1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757340	M	MP:0012362	increased large unstained cell number	Mapkapk2<tm1b(EUCOMM)Hmgu>/Mapkapk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapkapk2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757340	M	MP:0002932	abnormal joint morphology	Mapkapk2<tm1b(EUCOMM)Hmgu>/Mapkapk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapkapk2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757340	M	MP:0005011	increased eosinophil cell number	Mapkapk2<tm1b(EUCOMM)Hmgu>/Mapkapk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapkapk2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757340	M	MP:0008259	abnormal optic disk morphology	Mapkapk2<tm1b(EUCOMM)Hmgu>/Mapkapk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapkapk2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757340	F	MP:0005559	increased circulating glucose level	Mapkapk2<tm1b(EUCOMM)Hmgu>/Mapkapk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapkapk2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757340	M	MP:0005298	abnormal clavicle morphology	Mapkapk2<tm1b(EUCOMM)Hmgu>/Mapkapk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapkapk2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757341	M	MP:0002833	increased heart weight	Mapkbp1<tm1b(EUCOMM)Hmgu>/Mapkbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapkbp1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757341	M	MP:0005565	increased blood urea nitrogen level	Mapkbp1<tm1b(EUCOMM)Hmgu>/Mapkbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapkbp1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757341	M	MP:0004952	increased spleen weight	Mapkbp1<tm1b(EUCOMM)Hmgu>/Mapkbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapkbp1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757341	M	MP:0003917	increased kidney weight	Mapkbp1<tm1b(EUCOMM)Hmgu>/Mapkbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapkbp1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757342	M	MP:0002792	abnormal retina vasculature morphology	Mapt<tm1b(EUCOMM)Hmgu>/Mapt<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapt<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757342	F	MP:0008528	polycystic kidney	Mapt<tm1b(EUCOMM)Hmgu>/Mapt<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapt<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757342	M	MP:0010053	decreased grip strength	Mapt<tm1b(EUCOMM)Hmgu>/Mapt<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapt<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757342	M	MP:0001417	decreased exploration in new environment	Mapt<tm1b(EUCOMM)Hmgu>/Mapt<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapt<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757342	M	MP:0001289	persistence of hyaloid vascular system	Mapt<tm1b(EUCOMM)Hmgu>/Mapt<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapt<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757342	M	MP:0010097	abnormal retina blood vessel morphology	Mapt<tm1b(EUCOMM)Hmgu>/Mapt<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapt<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757342	M	MP:0011965	decreased total retina thickness	Mapt<tm1b(EUCOMM)Hmgu>/Mapt<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapt<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757343	M	MP:0000274	enlarged heart	Marveld2<tm1b(EUCOMM)Wtsi>/Marveld2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Marveld2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757344	M	MP:0005333	decreased heart rate	Masp1<tm1.1(KOMP)Vlcg>/Masp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Masp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757344	M	MP:0005633	increased circulating sodium level	Masp1<tm1.1(KOMP)Vlcg>/Masp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Masp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757344	M	MP:0010506	prolonged RR interval	Masp1<tm1.1(KOMP)Vlcg>/Masp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Masp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757344	M	MP:0013278	decreased fasting circulating glucose level	Masp1<tm1.1(KOMP)Vlcg>/Masp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Masp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757344	M	MP:0002968	increased circulating alkaline phosphatase level	Masp1<tm1.1(KOMP)Vlcg>/Masp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Masp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757344	F	MP:0001258	decreased body length	Masp1<tm1.1(KOMP)Vlcg>/Masp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Masp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757346	M	MP:0005016	decreased lymphocyte cell number	Mbd5<tm1b(EUCOMM)Wtsi>/Mbd5<+>	C57BL/6N-Mbd5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757346	M	MP:0002764	short tibia	Mbd5<tm1b(EUCOMM)Wtsi>/Mbd5<+>	C57BL/6N-Mbd5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757346	M	MP:0000221	decreased leukocyte cell number	Mbd5<tm1b(EUCOMM)Wtsi>/Mbd5<+>	C57BL/6N-Mbd5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757346	M	MP:0011965	decreased total retina thickness	Mbd5<tm1b(EUCOMM)Wtsi>/Mbd5<+>	C57BL/6N-Mbd5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757346	M	MP:0001417	decreased exploration in new environment	Mbd5<tm1b(EUCOMM)Wtsi>/Mbd5<+>	C57BL/6N-Mbd5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757346	F	MP:0003769	abnormal lip morphology	Mbd5<tm1b(EUCOMM)Wtsi>/Mbd5<+>	C57BL/6N-Mbd5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757350	M	MP:0010124	decreased bone mineral content	Mcu<tm1b(EUCOMM)Hmgu>/Mcu<+>	C57BL/6N-Mcu<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757350	M	MP:0013279	increased fasting circulating glucose level	Mcu<tm1b(EUCOMM)Hmgu>/Mcu<+>	C57BL/6N-Mcu<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757350	M	MP:0001556	increased circulating HDL cholesterol level	Mcu<tm1b(EUCOMM)Hmgu>/Mcu<+>	C57BL/6N-Mcu<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757350	M	MP:0010024	increased total body fat amount	Mcu<tm1b(EUCOMM)Hmgu>/Mcu<+>	C57BL/6N-Mcu<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757350	M	MP:0003961	decreased lean body mass	Mcu<tm1b(EUCOMM)Hmgu>/Mcu<+>	C57BL/6N-Mcu<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757352	M	MP:0001417	decreased exploration in new environment	Med25<tm1b(KOMP)Wtsi>/Med25<+>	C57BL/6N-Med25<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757352	F	MP:0010024	increased total body fat amount	Med25<tm1b(KOMP)Wtsi>/Med25<+>	C57BL/6N-Med25<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757352	F	MP:0002764	short tibia	Med25<tm1b(KOMP)Wtsi>/Med25<+>	C57BL/6N-Med25<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757354	M	MP:0000692	small spleen	Med28<tm1.1(KOMP)Vlcg>/Med28<+>	C57BL/6N-Med28<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757354	M	MP:0000689	abnormal spleen morphology	Med28<tm1.1(KOMP)Vlcg>/Med28<+>	C57BL/6N-Med28<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757354	F	MP:0005419	decreased circulating serum albumin level	Med28<tm1.1(KOMP)Vlcg>/Med28<+>	C57BL/6N-Med28<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757354	M	MP:0010378	increased respiratory quotient	Med28<tm1.1(KOMP)Vlcg>/Med28<+>	C57BL/6N-Med28<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757359	M	MP:0002875	decreased erythrocyte cell number	Mettl16<tm1b(KOMP)Mbp>/Mettl16<+>	C57BL/6N-Mettl16<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757359	M	MP:0005178	increased circulating cholesterol level	Mettl16<tm1b(KOMP)Mbp>/Mettl16<+>	C57BL/6N-Mettl16<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757359	M	MP:0002874	decreased hemoglobin content	Mettl16<tm1b(KOMP)Mbp>/Mettl16<+>	C57BL/6N-Mettl16<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757359	M	MP:0001556	increased circulating HDL cholesterol level	Mettl16<tm1b(KOMP)Mbp>/Mettl16<+>	C57BL/6N-Mettl16<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757359	F	MP:0002075	abnormal coat/hair pigmentation	Mettl16<tm1b(KOMP)Mbp>/Mettl16<+>	C57BL/6N-Mettl16<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757359	M	MP:0000208	decreased hematocrit	Mettl16<tm1b(KOMP)Mbp>/Mettl16<+>	C57BL/6N-Mettl16<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757361	M	MP:0002075	abnormal coat/hair pigmentation	Tmt1b<tm1.1(KOMP)Vlcg>/Tmt1b<tm1.1(KOMP)Vlcg>	C57BL/6N-Timt1b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757361	M	MP:0005560	decreased circulating glucose level	Tmt1b<tm1.1(KOMP)Vlcg>/Tmt1b<tm1.1(KOMP)Vlcg>	C57BL/6N-Timt1b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757362	M	MP:0006243	impaired pupillary reflex	Mfsd8<tm1b(EUCOMM)Hmgu>/Mfsd8<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mfsd8<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757363	F	MP:0011886	increased circulating lipase level	Mipol1<tm1b(EUCOMM)Hmgu>/Mipol1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mipol1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757363	F	MP:0001304	cataract	Mipol1<tm1b(EUCOMM)Hmgu>/Mipol1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mipol1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757363	F	MP:0005343	increased circulating aspartate transaminase level	Mipol1<tm1b(EUCOMM)Hmgu>/Mipol1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mipol1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757364	M	MP:0005343	increased circulating aspartate transaminase level	Mlh1<tm1b(EUCOMM)Hmgu>/Mlh1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mlh1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757364	F	MP:0004952	increased spleen weight	Mlh1<tm1b(EUCOMM)Hmgu>/Mlh1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mlh1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757364	M	MP:0001147	small testis	Mlh1<tm1b(EUCOMM)Hmgu>/Mlh1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mlh1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757364	F	MP:0001304	cataract	Mlh1<tm1b(EUCOMM)Hmgu>/Mlh1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mlh1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757364	M	MP:0002941	increased circulating alanine transaminase level	Mlh1<tm1b(EUCOMM)Hmgu>/Mlh1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mlh1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757364	M	MP:0001925	male infertility	Mlh1<tm1b(EUCOMM)Hmgu>/Mlh1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mlh1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757365	M	MP:0003918	decreased kidney weight	Mllt3<tm1b(EUCOMM)Hmgu>/Mllt3<+>	C57BL/6N-Mllt3<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757365	M	MP:0008806	increased circulating amylase level	Mllt3<tm1b(EUCOMM)Hmgu>/Mllt3<+>	C57BL/6N-Mllt3<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757365	F	MP:0010024	increased total body fat amount	Mllt3<tm1b(EUCOMM)Hmgu>/Mllt3<+>	C57BL/6N-Mllt3<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757368	F	MP:0002092	abnormal eye morphology	Mmp16<tm1b(EUCOMM)Wtsi>/Mmp16<tm1b(EUCOMM)Wtsi>	C57BL/6N-Mmp16<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757368	F	MP:0003043	hypoalgesia	Mmp16<tm1b(EUCOMM)Wtsi>/Mmp16<tm1b(EUCOMM)Wtsi>	C57BL/6N-Mmp16<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757370	M	MP:0012362	increased large unstained cell number	Mmrn1<tm1b(EUCOMM)Hmgu>/Mmrn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mmrn1<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757370	M	MP:0001925	male infertility	Mmrn1<tm1b(EUCOMM)Hmgu>/Mmrn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mmrn1<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757371	M	MP:0005634	decreased circulating sodium level	Mocs2<tm1b(EUCOMM)Wtsi>/Mocs2<+>	C57BL/6N-Mocs2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757371	M	MP:0001258	decreased body length	Mocs2<tm1b(EUCOMM)Wtsi>/Mocs2<+>	C57BL/6N-Mocs2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757377	M	MP:0010053	decreased grip strength	Mrps5<tm1b(EUCOMM)Wtsi>/Mrps5<+>	C57BL/6N-Mrps5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757379	F	MP:0010053	decreased grip strength	Msantd1<tm1.1(KOMP)Vlcg>/Msantd1<tm1.1(KOMP)Vlcg>	C57BL/6N-Msantd1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757379	M	MP:0000266	abnormal heart morphology	Msantd1<tm1.1(KOMP)Vlcg>/Msantd1<tm1.1(KOMP)Vlcg>	C57BL/6N-Msantd1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757379	M	MP:0000274	enlarged heart	Msantd1<tm1.1(KOMP)Vlcg>/Msantd1<tm1.1(KOMP)Vlcg>	C57BL/6N-Msantd1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757381	F	MP:0005343	increased circulating aspartate transaminase level	Mtf1<tm1b(KOMP)Wtsi>/Mtf1<+>	C57BL/6N-Mtf1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757381	M	MP:0001325	abnormal retina morphology	Mtf1<tm1b(KOMP)Wtsi>/Mtf1<+>	C57BL/6N-Mtf1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757381	M	MP:0005560	decreased circulating glucose level	Mtf1<tm1b(KOMP)Wtsi>/Mtf1<+>	C57BL/6N-Mtf1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757382	M	MP:0001297	microphthalmia	Mtf1<tm1b(KOMP)Wtsi>/Mtf1<tm1b(KOMP)Wtsi>	C57BL/6N-Mtf1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757382	F	MP:0000428	abnormal craniofacial morphology	Mtf1<tm1b(KOMP)Wtsi>/Mtf1<tm1b(KOMP)Wtsi>	C57BL/6N-Mtf1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757382	M	MP:0001293	anophthalmia	Mtf1<tm1b(KOMP)Wtsi>/Mtf1<tm1b(KOMP)Wtsi>	C57BL/6N-Mtf1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757383	M	MP:0001303	abnormal lens morphology	Mthfsl<tm1b(EUCOMM)Hmgu>/Mthfsl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mthfsl<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757383	M	MP:0010053	decreased grip strength	Mthfsl<tm1b(EUCOMM)Hmgu>/Mthfsl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mthfsl<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757383	M	MP:0001304	cataract	Mthfsl<tm1b(EUCOMM)Hmgu>/Mthfsl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mthfsl<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757384	F	MP:0010090	increased circulating creatine kinase level	Mxra7<tm1b(EUCOMM)Wtsi>/Mxra7<tm1b(EUCOMM)Wtsi>	C57BL/6N-Mxra7<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757385	M	MP:0002968	increased circulating alkaline phosphatase level	Mybbp1a<tm1b(EUCOMM)Hmgu>/Mybbp1a<+>	C57BL/6N-Mybbp1a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757385	M	MP:0005505	thrombocytosis	Mybbp1a<tm1b(EUCOMM)Hmgu>/Mybbp1a<+>	C57BL/6N-Mybbp1a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757385	M	MP:0002608	increased hematocrit	Mybbp1a<tm1b(EUCOMM)Hmgu>/Mybbp1a<+>	C57BL/6N-Mybbp1a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757385	F	MP:0005633	increased circulating sodium level	Mybbp1a<tm1b(EUCOMM)Hmgu>/Mybbp1a<+>	C57BL/6N-Mybbp1a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757385	M	MP:0003131	increased erythrocyte cell number	Mybbp1a<tm1b(EUCOMM)Hmgu>/Mybbp1a<+>	C57BL/6N-Mybbp1a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757385	M	MP:0005564	increased hemoglobin content	Mybbp1a<tm1b(EUCOMM)Hmgu>/Mybbp1a<+>	C57BL/6N-Mybbp1a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757385	F	MP:0001488	increased startle reflex	Mybbp1a<tm1b(EUCOMM)Hmgu>/Mybbp1a<+>	C57BL/6N-Mybbp1a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757389	F	MP:0003795	abnormal bone structure	Myh1<tm1b(KOMP)Wtsi>/Myh1<tm1b(KOMP)Wtsi>	C57BL/6N-Myh1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757389	M	MP:0005564	increased hemoglobin content	Myh1<tm1b(KOMP)Wtsi>/Myh1<tm1b(KOMP)Wtsi>	C57BL/6N-Myh1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757389	F	MP:0003870	decreased urine glucose level	Myh1<tm1b(KOMP)Wtsi>/Myh1<tm1b(KOMP)Wtsi>	C57BL/6N-Myh1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757389	F	MP:0011396	abnormal sleep behavior	Myh1<tm1b(KOMP)Wtsi>/Myh1<tm1b(KOMP)Wtsi>	C57BL/6N-Myh1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757389	M	MP:0000221	decreased leukocyte cell number	Myh1<tm1b(KOMP)Wtsi>/Myh1<tm1b(KOMP)Wtsi>	C57BL/6N-Myh1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757389	M	MP:0002608	increased hematocrit	Myh1<tm1b(KOMP)Wtsi>/Myh1<tm1b(KOMP)Wtsi>	C57BL/6N-Myh1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757389	F	MP:0010124	decreased bone mineral content	Myh1<tm1b(KOMP)Wtsi>/Myh1<tm1b(KOMP)Wtsi>	C57BL/6N-Myh1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757389	F	MP:0010024	increased total body fat amount	Myh1<tm1b(KOMP)Wtsi>/Myh1<tm1b(KOMP)Wtsi>	C57BL/6N-Myh1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757389	F	MP:0001417	decreased exploration in new environment	Myh1<tm1b(KOMP)Wtsi>/Myh1<tm1b(KOMP)Wtsi>	C57BL/6N-Myh1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757390	F	MP:0002968	increased circulating alkaline phosphatase level	Mylip<tm1.1(KOMP)Vlcg>/Mylip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mylip<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757390	F	MP:0001415	increased exploration in new environment	Mylip<tm1.1(KOMP)Vlcg>/Mylip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mylip<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757392	M	MP:0003019	increased circulating chloride level	Myo7b<tm1b(EUCOMM)Hmgu>/Myo7b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Myo7b<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757393	M	MP:0008528	polycystic kidney	Myoz1<tm1b(EUCOMM)Hmgu>/Myoz1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Myoz1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757393	M	MP:0002997	enlarged seminal vesicle	Myoz1<tm1b(EUCOMM)Hmgu>/Myoz1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Myoz1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757393	M	MP:0005554	decreased circulating creatinine level	Myoz1<tm1b(EUCOMM)Hmgu>/Myoz1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Myoz1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757395	M	MP:0000186	decreased circulating HDL cholesterol level	Nab2<tm1b(EUCOMM)Hmgu>/Nab2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nab2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757395	F	MP:0002066	abnormal motor capabilities/coordination/movement	Nab2<tm1b(EUCOMM)Hmgu>/Nab2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nab2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757395	F	MP:0001402	decreased locomotor activity	Nab2<tm1b(EUCOMM)Hmgu>/Nab2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nab2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757395	F	MP:0001454	abnormal cued conditioning behavior	Nab2<tm1b(EUCOMM)Hmgu>/Nab2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nab2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757395	F	MP:0001312	abnormal cornea morphology	Nab2<tm1b(EUCOMM)Hmgu>/Nab2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nab2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757395	F	MP:0020420	abnormal freezing behavior	Nab2<tm1b(EUCOMM)Hmgu>/Nab2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nab2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757395	M	MP:0005179	decreased circulating cholesterol level	Nab2<tm1b(EUCOMM)Hmgu>/Nab2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nab2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757395	F	MP:0001417	decreased exploration in new environment	Nab2<tm1b(EUCOMM)Hmgu>/Nab2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nab2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757395	M	MP:0000598	abnormal liver morphology	Nab2<tm1b(EUCOMM)Hmgu>/Nab2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nab2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757395	F	MP:0001469	abnormal contextual conditioning behavior	Nab2<tm1b(EUCOMM)Hmgu>/Nab2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nab2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757395	M	MP:0001406	abnormal gait	Nab2<tm1b(EUCOMM)Hmgu>/Nab2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nab2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757396	M	MP:0001510	abnormal coat appearance	Nacc2<tm2b(EUCOMM)Wtsi>/Nacc2<tm2b(EUCOMM)Wtsi>	C57BL/6N-Nacc2<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757396	F	MP:0002968	increased circulating alkaline phosphatase level	Nacc2<tm2b(EUCOMM)Wtsi>/Nacc2<tm2b(EUCOMM)Wtsi>	C57BL/6N-Nacc2<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757397	M	MP:0001417	decreased exploration in new environment	Nae1<tm1b(EUCOMM)Wtsi>/Nae1<+>	C57BL/6N-Nae1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757397	M	MP:0001566	increased circulating phosphate level	Nae1<tm1b(EUCOMM)Wtsi>/Nae1<+>	C57BL/6N-Nae1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757397	M	MP:0002590	increased mean corpuscular volume	Nae1<tm1b(EUCOMM)Wtsi>/Nae1<+>	C57BL/6N-Nae1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757397	M	MP:0013279	increased fasting circulating glucose level	Nae1<tm1b(EUCOMM)Wtsi>/Nae1<+>	C57BL/6N-Nae1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757399	M	MP:0000219	increased neutrophil cell number	Nagk<tm1b(EUCOMM)Hmgu>/Nagk<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nagk<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757399	M	MP:0005567	decreased circulating total protein level	Nagk<tm1b(EUCOMM)Hmgu>/Nagk<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nagk<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757399	M	MP:0005419	decreased circulating serum albumin level	Nagk<tm1b(EUCOMM)Hmgu>/Nagk<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nagk<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757400	M	MP:0003960	increased lean body mass	Natd1<tm1b(EUCOMM)Wtsi>/Natd1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Natd1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757400	M	MP:0010067	increased red blood cell distribution width	Natd1<tm1b(EUCOMM)Wtsi>/Natd1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Natd1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757400	M	MP:0010025	decreased total body fat amount	Natd1<tm1b(EUCOMM)Wtsi>/Natd1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Natd1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757402	M	MP:0008806	increased circulating amylase level	Ncf4<tm1b(KOMP)Wtsi>/Ncf4<tm1b(KOMP)Wtsi>	C57BL/6N-Ncf4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757403	M	MP:0010053	decreased grip strength	Ncs1<tm1b(EUCOMM)Hmgu>/Ncs1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ncs1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757403	M	MP:0001566	increased circulating phosphate level	Ncs1<tm1b(EUCOMM)Hmgu>/Ncs1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ncs1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757403	F	MP:0001312	abnormal cornea morphology	Ncs1<tm1b(EUCOMM)Hmgu>/Ncs1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ncs1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757403	M	MP:0011965	decreased total retina thickness	Ncs1<tm1b(EUCOMM)Hmgu>/Ncs1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ncs1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757404	F	MP:0001402	decreased locomotor activity	Ndfip2<tm1b(EUCOMM)Hmgu>/Ndfip2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ndfip2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757404	F	MP:0002135	abnormal kidney morphology	Ndfip2<tm1b(EUCOMM)Hmgu>/Ndfip2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ndfip2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757404	F	MP:0002574	increased vertical activity	Ndfip2<tm1b(EUCOMM)Hmgu>/Ndfip2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ndfip2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757404	M	MP:0010052	increased grip strength	Ndfip2<tm1b(EUCOMM)Hmgu>/Ndfip2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ndfip2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757404	F	MP:0001304	cataract	Ndfip2<tm1b(EUCOMM)Hmgu>/Ndfip2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ndfip2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757404	F	MP:0001303	abnormal lens morphology	Ndfip2<tm1b(EUCOMM)Hmgu>/Ndfip2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ndfip2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757405	F	MP:0005565	increased blood urea nitrogen level	Ndrg4<tm1b(KOMP)Wtsi>/Ndrg4<tm1b(KOMP)Wtsi>	C57BL/6N-Ndrg4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757405	F	MP:0005140	decreased cardiac muscle contractility	Ndrg4<tm1b(KOMP)Wtsi>/Ndrg4<tm1b(KOMP)Wtsi>	C57BL/6N-Ndrg4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757405	F	MP:0005553	increased circulating creatinine level	Ndrg4<tm1b(KOMP)Wtsi>/Ndrg4<tm1b(KOMP)Wtsi>	C57BL/6N-Ndrg4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757405	M	MP:0001513	limb grasping	Ndrg4<tm1b(KOMP)Wtsi>/Ndrg4<tm1b(KOMP)Wtsi>	C57BL/6N-Ndrg4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757406	F	MP:0010097	abnormal retina blood vessel morphology	Ndufa8<tm1b(EUCOMM)Hmgu>/Ndufa8<+>	C57BL/6N-Ndufa8<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757406	M	MP:0010506	prolonged RR interval	Ndufa8<tm1b(EUCOMM)Hmgu>/Ndufa8<+>	C57BL/6N-Ndufa8<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757406	M	MP:0003928	increased heart rate variability	Ndufa8<tm1b(EUCOMM)Hmgu>/Ndufa8<+>	C57BL/6N-Ndufa8<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757406	F	MP:0010123	increased bone mineral content	Ndufa8<tm1b(EUCOMM)Hmgu>/Ndufa8<+>	C57BL/6N-Ndufa8<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757408	M	MP:0002757	decreased vertical activity	Ndufs1<tm1b(EUCOMM)Hmgu>/Ndufs1<+>	C57BL/6N-Ndufs1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757408	M	MP:0001402	decreased locomotor activity	Ndufs1<tm1b(EUCOMM)Hmgu>/Ndufs1<+>	C57BL/6N-Ndufs1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757408	M	MP:0001304	cataract	Ndufs1<tm1b(EUCOMM)Hmgu>/Ndufs1<+>	C57BL/6N-Ndufs1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757408	M	MP:0002644	decreased circulating triglyceride level	Ndufs1<tm1b(EUCOMM)Hmgu>/Ndufs1<+>	C57BL/6N-Ndufs1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757408	F	MP:0011886	increased circulating lipase level	Ndufs1<tm1b(EUCOMM)Hmgu>/Ndufs1<+>	C57BL/6N-Ndufs1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757412	M	MP:0001489	decreased startle reflex	Nedd4l<tm1b(KOMP)Wtsi>/Nedd4l<tm1b(KOMP)Wtsi>	C57BL/6N-Nedd4l<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757412	F	MP:0001417	decreased exploration in new environment	Nedd4l<tm1b(KOMP)Wtsi>/Nedd4l<tm1b(KOMP)Wtsi>	C57BL/6N-Nedd4l<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757412	M	MP:0001486	abnormal startle reflex	Nedd4l<tm1b(KOMP)Wtsi>/Nedd4l<tm1b(KOMP)Wtsi>	C57BL/6N-Nedd4l<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757412	M	MP:0001325	abnormal retina morphology	Nedd4l<tm1b(KOMP)Wtsi>/Nedd4l<tm1b(KOMP)Wtsi>	C57BL/6N-Nedd4l<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757414	F	MP:0000221	decreased leukocyte cell number	Neurl2<tm1.1(KOMP)Vlcg>/Neurl2<tm1.1(KOMP)Vlcg>	C57BL/6N-Neurl2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757414	F	MP:0004151	decreased circulating iron level	Neurl2<tm1.1(KOMP)Vlcg>/Neurl2<tm1.1(KOMP)Vlcg>	C57BL/6N-Neurl2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757414	F	MP:0001510	abnormal coat appearance	Neurl2<tm1.1(KOMP)Vlcg>/Neurl2<tm1.1(KOMP)Vlcg>	C57BL/6N-Neurl2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757414	F	MP:0005560	decreased circulating glucose level	Neurl2<tm1.1(KOMP)Vlcg>/Neurl2<tm1.1(KOMP)Vlcg>	C57BL/6N-Neurl2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757415	F	MP:0001488	increased startle reflex	Nfatc3<tm1b(EUCOMM)Hmgu>/Nfatc3<+>	C57BL/6N-Nfatc3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757417	M	MP:0002833	increased heart weight	Nfatc4<tm1.1(KOMP)Vlcg>/Nfatc4<tm1.1(KOMP)Vlcg>	C57BL/6N-Nfatc4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757418	M	MP:0004924	abnormal behavior	Ngfr<tm1b(EUCOMM)Wtsi>/Ngfr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ngfr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757418	F	MP:0001566	increased circulating phosphate level	Ngfr<tm1b(EUCOMM)Wtsi>/Ngfr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ngfr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757418	M	MP:0001402	decreased locomotor activity	Ngfr<tm1b(EUCOMM)Wtsi>/Ngfr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ngfr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757418	M	MP:0020870	decreased thigmotaxis	Ngfr<tm1b(EUCOMM)Wtsi>/Ngfr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ngfr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757418	M	MP:0000745	tremors	Ngfr<tm1b(EUCOMM)Wtsi>/Ngfr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ngfr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757419	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	M	MP:0005278	abnormal cholesterol homeostasis	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	F	MP:0001926	female infertility	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	F	MP:0002590	increased mean corpuscular volume	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	M	MP:0004952	increased spleen weight	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	F	MP:0003795	abnormal bone structure	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	F	MP:0002637	small uterus	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	M	MP:0002631	abnormal epididymis morphology	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	F	MP:0001126	abnormal ovary morphology	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	M	MP:0001146	abnormal testis morphology	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	M	MP:0003642	absent seminal vesicle	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	F	MP:0001120	abnormal uterus morphology	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	F	MP:0003578	absent ovary	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	M	MP:0006415	absent testes	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	M	MP:0002941	increased circulating alanine transaminase level	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	M	MP:0011110	preweaning lethality, incomplete penetrance	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	M	MP:0001925	male infertility	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	M	MP:0004727	absent epididymis	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	M	MP:0002059	abnormal seminal vesicle morphology	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	M	MP:0003918	decreased kidney weight	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757419	M	MP:0005343	increased circulating aspartate transaminase level	Nhlh2<tm1b(KOMP)Mbp>/Nhlh2<tm1b(KOMP)Mbp>	C57BL/6N-Nhlh2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5757422	F	MP:0001566	increased circulating phosphate level	Nmrk2<tm1.1(KOMP)Vlcg>/Nmrk2<tm1.1(KOMP)Vlcg>	C57BL/6N-Nmrk2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757423	M	MP:0013278	decreased fasting circulating glucose level	Nobox<tm1.1(KOMP)Vlcg>/Nobox<+>	C57BL/6N-Nobox<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757423	F	MP:0001399	hyperactivity	Nobox<tm1.1(KOMP)Vlcg>/Nobox<+>	C57BL/6N-Nobox<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757424	M	MP:0002059	abnormal seminal vesicle morphology	Nobox<tm1.1(KOMP)Vlcg>/Nobox<tm1.1(KOMP)Vlcg>	C57BL/6N-Nobox<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757425	M	MP:0010097	abnormal retina blood vessel morphology	Nos1ap<tm1b(KOMP)Wtsi>/Nos1ap<tm1b(KOMP)Wtsi>	C57BL/6N-Nos1ap<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757425	F	MP:0010124	decreased bone mineral content	Nos1ap<tm1b(KOMP)Wtsi>/Nos1ap<tm1b(KOMP)Wtsi>	C57BL/6N-Nos1ap<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757425	M	MP:0000538	abnormal urinary bladder morphology	Nos1ap<tm1b(KOMP)Wtsi>/Nos1ap<tm1b(KOMP)Wtsi>	C57BL/6N-Nos1ap<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757425	M	MP:0002574	increased vertical activity	Nos1ap<tm1b(KOMP)Wtsi>/Nos1ap<tm1b(KOMP)Wtsi>	C57BL/6N-Nos1ap<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757425	M	MP:0002942	decreased circulating alanine transaminase level	Nos1ap<tm1b(KOMP)Wtsi>/Nos1ap<tm1b(KOMP)Wtsi>	C57BL/6N-Nos1ap<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757425	M	MP:0001399	hyperactivity	Nos1ap<tm1b(KOMP)Wtsi>/Nos1ap<tm1b(KOMP)Wtsi>	C57BL/6N-Nos1ap<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757426	F	MP:0001417	decreased exploration in new environment	Npc1<tm1b(EUCOMM)Hmgu>/Npc1<+>	C57BL/6N-Npc1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757428	F	MP:0001303	abnormal lens morphology	Npm3<tm1.1(KOMP)Vlcg>/Npm3<tm1.1(KOMP)Vlcg>	C57BL/6N-Npm3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757428	M	MP:0005560	decreased circulating glucose level	Npm3<tm1.1(KOMP)Vlcg>/Npm3<tm1.1(KOMP)Vlcg>	C57BL/6N-Npm3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757429	F	MP:0001406	abnormal gait	Nptn<tm1b(EUCOMM)Hmgu>/Nptn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nptn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757429	M	MP:0001566	increased circulating phosphate level	Nptn<tm1b(EUCOMM)Hmgu>/Nptn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nptn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757429	F	MP:0001322	abnormal iris morphology	Nptn<tm1b(EUCOMM)Hmgu>/Nptn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nptn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757429	M	MP:0002833	increased heart weight	Nptn<tm1b(EUCOMM)Hmgu>/Nptn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nptn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757429	M	MP:0001486	abnormal startle reflex	Nptn<tm1b(EUCOMM)Hmgu>/Nptn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nptn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757429	F	MP:0005564	increased hemoglobin content	Nptn<tm1b(EUCOMM)Hmgu>/Nptn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nptn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757429	F	MP:0000745	tremors	Nptn<tm1b(EUCOMM)Hmgu>/Nptn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nptn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757429	F	MP:0005178	increased circulating cholesterol level	Nptn<tm1b(EUCOMM)Hmgu>/Nptn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nptn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757429	M	MP:0010025	decreased total body fat amount	Nptn<tm1b(EUCOMM)Hmgu>/Nptn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nptn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757429	F	MP:0002590	increased mean corpuscular volume	Nptn<tm1b(EUCOMM)Hmgu>/Nptn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nptn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757429	F	MP:0008810	increased circulating iron level	Nptn<tm1b(EUCOMM)Hmgu>/Nptn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nptn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757430	M	MP:0003393	decreased cardiac output	Nr1d1<tm1(KOMP)Vlcg>/Nr1d1<tm1(KOMP)Vlcg>	C57BL/6N-Nr1d1<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5757430	M	MP:0008045	decreased NK cell number	Nr1d1<tm1(KOMP)Vlcg>/Nr1d1<tm1(KOMP)Vlcg>	C57BL/6N-Nr1d1<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5757430	F	MP:0002092	abnormal eye morphology	Nr1d1<tm1(KOMP)Vlcg>/Nr1d1<tm1(KOMP)Vlcg>	C57BL/6N-Nr1d1<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5757430	F	MP:0000274	enlarged heart	Nr1d1<tm1(KOMP)Vlcg>/Nr1d1<tm1(KOMP)Vlcg>	C57BL/6N-Nr1d1<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5757430	M	MP:0020870	decreased thigmotaxis	Nr1d1<tm1(KOMP)Vlcg>/Nr1d1<tm1(KOMP)Vlcg>	C57BL/6N-Nr1d1<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5757430	F	MP:0003733	abnormal retina inner nuclear layer morphology	Nr1d1<tm1(KOMP)Vlcg>/Nr1d1<tm1(KOMP)Vlcg>	C57BL/6N-Nr1d1<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5757430	F	MP:0011960	abnormal eye anterior chamber depth	Nr1d1<tm1(KOMP)Vlcg>/Nr1d1<tm1(KOMP)Vlcg>	C57BL/6N-Nr1d1<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5757430	F	MP:0011959	abnormal eye posterior chamber depth	Nr1d1<tm1(KOMP)Vlcg>/Nr1d1<tm1(KOMP)Vlcg>	C57BL/6N-Nr1d1<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5757430	F	MP:0010123	increased bone mineral content	Nr1d1<tm1(KOMP)Vlcg>/Nr1d1<tm1(KOMP)Vlcg>	C57BL/6N-Nr1d1<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5757433	F	MP:0003795	abnormal bone structure	Nrxn1<tm1b(KOMP)Wtsi>/Nrxn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nrxn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757433	F	MP:0013278	decreased fasting circulating glucose level	Nrxn1<tm1b(KOMP)Wtsi>/Nrxn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nrxn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757433	M	MP:0005419	decreased circulating serum albumin level	Nrxn1<tm1b(KOMP)Wtsi>/Nrxn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nrxn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757433	M	MP:0005567	decreased circulating total protein level	Nrxn1<tm1b(KOMP)Wtsi>/Nrxn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nrxn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757433	F	MP:0002966	decreased circulating alkaline phosphatase level	Nrxn1<tm1b(KOMP)Wtsi>/Nrxn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nrxn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757433	M	MP:0010025	decreased total body fat amount	Nrxn1<tm1b(KOMP)Wtsi>/Nrxn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nrxn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757433	M	MP:0005179	decreased circulating cholesterol level	Nrxn1<tm1b(KOMP)Wtsi>/Nrxn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nrxn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757433	M	MP:0000186	decreased circulating HDL cholesterol level	Nrxn1<tm1b(KOMP)Wtsi>/Nrxn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nrxn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757433	F	MP:0005574	decreased pulmonary respiratory rate	Nrxn1<tm1b(KOMP)Wtsi>/Nrxn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nrxn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757434	F	MP:0001926	female infertility	Ntf5<tm1b(EUCOMM)Hmgu>/Ntf5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ntf5<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757434	F	MP:0005178	increased circulating cholesterol level	Ntf5<tm1b(EUCOMM)Hmgu>/Ntf5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ntf5<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757434	M	MP:0000745	tremors	Ntf5<tm1b(EUCOMM)Hmgu>/Ntf5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ntf5<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757434	M	MP:0010392	prolonged QRS complex duration	Ntf5<tm1b(EUCOMM)Hmgu>/Ntf5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ntf5<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757434	F	MP:0001556	increased circulating HDL cholesterol level	Ntf5<tm1b(EUCOMM)Hmgu>/Ntf5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ntf5<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757435	M	MP:0003179	thrombocytopenia	Ntn4<tm1b(KOMP)Wtsi>/Ntn4<tm1b(KOMP)Wtsi>	C57BL/6N-Ntn4<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757435	M	MP:0000208	decreased hematocrit	Ntn4<tm1b(KOMP)Wtsi>/Ntn4<tm1b(KOMP)Wtsi>	C57BL/6N-Ntn4<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757435	F	MP:0000689	abnormal spleen morphology	Ntn4<tm1b(KOMP)Wtsi>/Ntn4<tm1b(KOMP)Wtsi>	C57BL/6N-Ntn4<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757437	M	MP:0009142	decreased prepulse inhibition	Ntrk2<tm1b(EUCOMM)Wtsi>/Ntrk2<+>	C57BL/6N-Ntrk2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757437	M	MP:0003960	increased lean body mass	Ntrk2<tm1b(EUCOMM)Wtsi>/Ntrk2<+>	C57BL/6N-Ntrk2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757437	F	MP:0000150	abnormal rib morphology	Ntrk2<tm1b(EUCOMM)Wtsi>/Ntrk2<+>	C57BL/6N-Ntrk2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757437	F	MP:0001556	increased circulating HDL cholesterol level	Ntrk2<tm1b(EUCOMM)Wtsi>/Ntrk2<+>	C57BL/6N-Ntrk2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757441	F	MP:0005333	decreased heart rate	Nutf2<tm1b(KOMP)Mbp>/Nutf2<+>	C57BL/6N-Nutf2<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5757443	F	MP:0000443	abnormal snout morphology	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757443	F	MP:0000438	abnormal cranium morphology	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757443	F	MP:0001340	abnormal eyelid morphology	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757444	F	MP:0000443	abnormal snout morphology	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757446	M	MP:0002768	small adrenal glands	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5757447	M	MP:0002764	short tibia	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757458	M	MP:0005178	increased circulating cholesterol level	Obp2a<tm1b(EUCOMM)Wtsi>/Obp2a<tm1b(EUCOMM)Wtsi>	C57BL/6N-Obp2a<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757459	F	MP:0005333	decreased heart rate	Oplah<tm1b(KOMP)Wtsi>/Oplah<tm1b(KOMP)Wtsi>	C57BL/6N-Oplah<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757459	F	MP:0011897	decreased circulating unsaturated transferrin level	Oplah<tm1b(KOMP)Wtsi>/Oplah<tm1b(KOMP)Wtsi>	C57BL/6N-Oplah<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757459	F	MP:0010068	decreased red blood cell distribution width	Oplah<tm1b(KOMP)Wtsi>/Oplah<tm1b(KOMP)Wtsi>	C57BL/6N-Oplah<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757459	M	MP:0001488	increased startle reflex	Oplah<tm1b(KOMP)Wtsi>/Oplah<tm1b(KOMP)Wtsi>	C57BL/6N-Oplah<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757459	M	MP:0001304	cataract	Oplah<tm1b(KOMP)Wtsi>/Oplah<tm1b(KOMP)Wtsi>	C57BL/6N-Oplah<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757459	M	MP:0001303	abnormal lens morphology	Oplah<tm1b(KOMP)Wtsi>/Oplah<tm1b(KOMP)Wtsi>	C57BL/6N-Oplah<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757460	F	MP:0001175	abnormal lung morphology	Otub1<tm1b(EUCOMM)Hmgu>/Otub1<+>	C57BL/6N-Otub1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757463	M	MP:0005011	increased eosinophil cell number	Otud6a<tm1(KOMP)Vlcg>/Otud6a<tm1(KOMP)Vlcg>	C57BL/6N-Otud6a<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757463	M	MP:0002606	increased basophil cell number	Otud6a<tm1(KOMP)Vlcg>/Otud6a<tm1(KOMP)Vlcg>	C57BL/6N-Otud6a<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757463	F	MP:0001399	hyperactivity	Otud6a<tm1(KOMP)Vlcg>/Otud6a<tm1(KOMP)Vlcg>	C57BL/6N-Otud6a<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757465	F	MP:0002591	decreased mean corpuscular volume	P2rx4<tm1b(EUCOMM)Wtsi>/P2rx4<tm1b(EUCOMM)Wtsi>	C57BL/6N-P2rx4<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757465	F	MP:0005298	abnormal clavicle morphology	P2rx4<tm1b(EUCOMM)Wtsi>/P2rx4<tm1b(EUCOMM)Wtsi>	C57BL/6N-P2rx4<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757468	M	MP:0005505	thrombocytosis	Pacsin2<tm1b(EUCOMM)Hmgu>/Pacsin2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pacsin2<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757468	M	MP:0003960	increased lean body mass	Pacsin2<tm1b(EUCOMM)Hmgu>/Pacsin2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pacsin2<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757468	M	MP:0002833	increased heart weight	Pacsin2<tm1b(EUCOMM)Hmgu>/Pacsin2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pacsin2<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757468	F	MP:0013279	increased fasting circulating glucose level	Pacsin2<tm1b(EUCOMM)Hmgu>/Pacsin2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pacsin2<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757469	M	MP:0009142	decreased prepulse inhibition	Pak1<tm1b(EUCOMM)Hmgu>/Pak1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pak1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757469	M	MP:0001552	increased circulating triglyceride level	Pak1<tm1b(EUCOMM)Hmgu>/Pak1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pak1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757469	M	MP:0010124	decreased bone mineral content	Pak1<tm1b(EUCOMM)Hmgu>/Pak1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pak1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757469	M	MP:0010024	increased total body fat amount	Pak1<tm1b(EUCOMM)Hmgu>/Pak1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pak1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757470	M	MP:0002702	decreased circulating free fatty acids level	Palb2<tm1.1(KOMP)Vlcg>/Palb2<+>	C57BL/6N-Palb2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757470	M	MP:0002079	increased circulating insulin level	Palb2<tm1.1(KOMP)Vlcg>/Palb2<+>	C57BL/6N-Palb2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757472	M	MP:0000194	increased circulating calcium level	Paqr6<tm1b(KOMP)Wtsi>/Paqr6<tm1b(KOMP)Wtsi>	C57BL/6N-Paqr6<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757473	M	MP:0005599	increased cardiac muscle contractility	Pard3b<tm1b(EUCOMM)Wtsi>/Pard3b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pard3b<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757473	F	MP:0001303	abnormal lens morphology	Pard3b<tm1b(EUCOMM)Wtsi>/Pard3b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pard3b<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757474	F	MP:0002607	decreased basophil cell number	Pard3<tm1b(KOMP)Wtsi>/Pard3<+>	C57BL/6N-Pard3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757474	M	MP:0004953	decreased spleen weight	Pard3<tm1b(KOMP)Wtsi>/Pard3<+>	C57BL/6N-Pard3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757474	M	MP:0008259	abnormal optic disk morphology	Pard3<tm1b(KOMP)Wtsi>/Pard3<+>	C57BL/6N-Pard3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757476	F	MP:0003733	abnormal retina inner nuclear layer morphology	Parp1<tm1b(EUCOMM)Hmgu>/Parp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Parp1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757477	M	MP:0013278	decreased fasting circulating glucose level	Patl1<tm1b(EUCOMM)Wtsi>/Patl1<+>	C57BL/6N-Patl1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757477	F	MP:0009142	decreased prepulse inhibition	Patl1<tm1b(EUCOMM)Wtsi>/Patl1<+>	C57BL/6N-Patl1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757477	M	MP:0010053	decreased grip strength	Patl1<tm1b(EUCOMM)Wtsi>/Patl1<+>	C57BL/6N-Patl1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757478	F	MP:0011100	preweaning lethality, complete penetrance	Patl1<tm1b(EUCOMM)Wtsi>/Patl1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Patl1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757481	F	MP:0002968	increased circulating alkaline phosphatase level	Pax4<tm1b(EUCOMM)Hmgu>/Pax4<+>	C57BL/6N-Pax4<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757483	F	MP:0005566	decreased blood urea nitrogen level	Pbx3<tm1b(EUCOMM)Wtsi>/Pbx3<+>	C57BL/6N-Pbx3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757483	M	MP:0002100	abnormal tooth morphology	Pbx3<tm1b(EUCOMM)Wtsi>/Pbx3<+>	C57BL/6N-Pbx3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757483	F	MP:0003578	absent ovary	Pbx3<tm1b(EUCOMM)Wtsi>/Pbx3<+>	C57BL/6N-Pbx3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757483	M	MP:0005344	increased circulating bilirubin level	Pbx3<tm1b(EUCOMM)Wtsi>/Pbx3<+>	C57BL/6N-Pbx3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757488	M	MP:0002792	abnormal retina vasculature morphology	Pcsk1<tm1b(EUCOMM)Wtsi>/Pcsk1<+>	C57BL/6N-Pcsk1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757488	F	MP:0001402	decreased locomotor activity	Pcsk1<tm1b(EUCOMM)Wtsi>/Pcsk1<+>	C57BL/6N-Pcsk1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757488	M	MP:0002699	abnormal vitreous body morphology	Pcsk1<tm1b(EUCOMM)Wtsi>/Pcsk1<+>	C57BL/6N-Pcsk1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757488	M	MP:0001289	persistence of hyaloid vascular system	Pcsk1<tm1b(EUCOMM)Wtsi>/Pcsk1<+>	C57BL/6N-Pcsk1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757488	F	MP:0020420	abnormal freezing behavior	Pcsk1<tm1b(EUCOMM)Wtsi>/Pcsk1<+>	C57BL/6N-Pcsk1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757488	M	MP:0010097	abnormal retina blood vessel morphology	Pcsk1<tm1b(EUCOMM)Wtsi>/Pcsk1<+>	C57BL/6N-Pcsk1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757490	M	MP:0002833	increased heart weight	Pcsk4<tm1b(KOMP)Wtsi>/Pcsk4<tm1b(KOMP)Wtsi>	C57BL/6N-Pcsk4<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757490	F	MP:0005633	increased circulating sodium level	Pcsk4<tm1b(KOMP)Wtsi>/Pcsk4<tm1b(KOMP)Wtsi>	C57BL/6N-Pcsk4<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757491	M	MP:0003960	increased lean body mass	Pcsk5<tm1b(KOMP)Mbp>/Pcsk5<+>	C57BL/6N-Pcsk5<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757491	M	MP:0000195	decreased circulating calcium level	Pcsk5<tm1b(KOMP)Mbp>/Pcsk5<+>	C57BL/6N-Pcsk5<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757491	F	MP:0001399	hyperactivity	Pcsk5<tm1b(KOMP)Mbp>/Pcsk5<+>	C57BL/6N-Pcsk5<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757491	M	MP:0010123	increased bone mineral content	Pcsk5<tm1b(KOMP)Mbp>/Pcsk5<+>	C57BL/6N-Pcsk5<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757491	M	MP:0002833	increased heart weight	Pcsk5<tm1b(KOMP)Mbp>/Pcsk5<+>	C57BL/6N-Pcsk5<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757491	M	MP:0000186	decreased circulating HDL cholesterol level	Pcsk5<tm1b(KOMP)Mbp>/Pcsk5<+>	C57BL/6N-Pcsk5<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757491	M	MP:0005179	decreased circulating cholesterol level	Pcsk5<tm1b(KOMP)Mbp>/Pcsk5<+>	C57BL/6N-Pcsk5<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757492	M	MP:0010024	increased total body fat amount	Pcx<tm1b(EUCOMM)Wtsi>/Pcx<+>	C57BL/6N-Pcx<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757492	M	MP:0010379	decreased respiratory quotient	Pcx<tm1b(EUCOMM)Wtsi>/Pcx<+>	C57BL/6N-Pcx<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757492	M	MP:0003961	decreased lean body mass	Pcx<tm1b(EUCOMM)Wtsi>/Pcx<+>	C57BL/6N-Pcx<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757493	M	MP:0010052	increased grip strength	Pcx<tm1b(EUCOMM)Wtsi>/Pcx<+>	C57BL/6N-Pcx<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757496	M	MP:0001340	abnormal eyelid morphology	Pdcd2<tm1b(EUCOMM)Wtsi>/Pdcd2<+>	C57BL/6N-Pdcd2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757500	F	MP:0001399	hyperactivity	Pde1b<tm1b(EUCOMM)Wtsi>/Pde1b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pde1b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757500	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Pde1b<tm1b(EUCOMM)Wtsi>/Pde1b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pde1b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757500	M	MP:0005561	increased mean corpuscular hemoglobin	Pde1b<tm1b(EUCOMM)Wtsi>/Pde1b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pde1b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757501	M	MP:0002059	abnormal seminal vesicle morphology	Pdgfrb<tm1b(EUCOMM)Hmgu>/Pdgfrb<+>	C57BL/6N-Pdgfrb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757501	M	MP:0000274	enlarged heart	Pdgfrb<tm1b(EUCOMM)Hmgu>/Pdgfrb<+>	C57BL/6N-Pdgfrb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757501	F	MP:0001552	increased circulating triglyceride level	Pdgfrb<tm1b(EUCOMM)Hmgu>/Pdgfrb<+>	C57BL/6N-Pdgfrb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757501	F	MP:0010088	decreased circulating fructosamine level	Pdgfrb<tm1b(EUCOMM)Hmgu>/Pdgfrb<+>	C57BL/6N-Pdgfrb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757503	F	MP:0000194	increased circulating calcium level	Pdpn<tm1b(EUCOMM)Wtsi>/Pdpn<+>	C57BL/6N-Pdpn<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757503	F	MP:0001284	absent vibrissae	Pdpn<tm1b(EUCOMM)Wtsi>/Pdpn<+>	C57BL/6N-Pdpn<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757503	M	MP:0005178	increased circulating cholesterol level	Pdpn<tm1b(EUCOMM)Wtsi>/Pdpn<+>	C57BL/6N-Pdpn<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757505	F	MP:0001258	decreased body length	Penk<tm1(KOMP)Mbp>/Penk<tm1(KOMP)Mbp>	C57BL/6N-Penk<tm1(KOMP)Mbp>/Rbrc	N	MGI:5576271
MGI:5757505	F	MP:0010124	decreased bone mineral content	Penk<tm1(KOMP)Mbp>/Penk<tm1(KOMP)Mbp>	C57BL/6N-Penk<tm1(KOMP)Mbp>/Rbrc	N	MGI:5576271
MGI:5757505	M	MP:0006415	absent testes	Penk<tm1(KOMP)Mbp>/Penk<tm1(KOMP)Mbp>	C57BL/6N-Penk<tm1(KOMP)Mbp>/Rbrc	N	MGI:5576271
MGI:5757505	F	MP:0003795	abnormal bone structure	Penk<tm1(KOMP)Mbp>/Penk<tm1(KOMP)Mbp>	C57BL/6N-Penk<tm1(KOMP)Mbp>/Rbrc	N	MGI:5576271
MGI:5757505	F	MP:0010024	increased total body fat amount	Penk<tm1(KOMP)Mbp>/Penk<tm1(KOMP)Mbp>	C57BL/6N-Penk<tm1(KOMP)Mbp>/Rbrc	N	MGI:5576271
MGI:5757506	M	MP:0000691	enlarged spleen	Pex26<tm1.1(KOMP)Vlcg>/Pex26<+>	C57BL/6N-Pex26<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757508	F	MP:0002590	increased mean corpuscular volume	Pfdn6<tm1.1(KOMP)Vlcg>/Pfdn6<+>	C57BL/6N-Pfdn6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757508	M	MP:0005560	decreased circulating glucose level	Pfdn6<tm1.1(KOMP)Vlcg>/Pfdn6<+>	C57BL/6N-Pfdn6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757508	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Pfdn6<tm1.1(KOMP)Vlcg>/Pfdn6<+>	C57BL/6N-Pfdn6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757510	M	MP:0000222	decreased neutrophil cell number	Pfkfb2<tm1b(KOMP)Wtsi>/Pfkfb2<tm1b(KOMP)Wtsi>	C57BL/6N-Pfkfb2<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757510	M	MP:0005013	increased lymphocyte cell number	Pfkfb2<tm1b(KOMP)Wtsi>/Pfkfb2<tm1b(KOMP)Wtsi>	C57BL/6N-Pfkfb2<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757510	M	MP:0002606	increased basophil cell number	Pfkfb2<tm1b(KOMP)Wtsi>/Pfkfb2<tm1b(KOMP)Wtsi>	C57BL/6N-Pfkfb2<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757510	F	MP:0013279	increased fasting circulating glucose level	Pfkfb2<tm1b(KOMP)Wtsi>/Pfkfb2<tm1b(KOMP)Wtsi>	C57BL/6N-Pfkfb2<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757510	M	MP:0005011	increased eosinophil cell number	Pfkfb2<tm1b(KOMP)Wtsi>/Pfkfb2<tm1b(KOMP)Wtsi>	C57BL/6N-Pfkfb2<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757511	M	MP:0002590	increased mean corpuscular volume	Pgam5<tm1b(EUCOMM)Wtsi>/Pgam5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pgam5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757511	M	MP:0005419	decreased circulating serum albumin level	Pgam5<tm1b(EUCOMM)Wtsi>/Pgam5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pgam5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757511	M	MP:0005179	decreased circulating cholesterol level	Pgam5<tm1b(EUCOMM)Wtsi>/Pgam5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pgam5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757511	M	MP:0005567	decreased circulating total protein level	Pgam5<tm1b(EUCOMM)Wtsi>/Pgam5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pgam5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757511	M	MP:0011965	decreased total retina thickness	Pgam5<tm1b(EUCOMM)Wtsi>/Pgam5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pgam5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757511	M	MP:0002875	decreased erythrocyte cell number	Pgam5<tm1b(EUCOMM)Wtsi>/Pgam5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pgam5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757511	M	MP:0000186	decreased circulating HDL cholesterol level	Pgam5<tm1b(EUCOMM)Wtsi>/Pgam5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pgam5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757511	M	MP:0005560	decreased circulating glucose level	Pgam5<tm1b(EUCOMM)Wtsi>/Pgam5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pgam5<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757515	M	MP:0005344	increased circulating bilirubin level	Pibf1<tm1.1(KOMP)Vlcg>/Pibf1<+>	C57BL/6N-Pibf1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757515	M	MP:0002833	increased heart weight	Pibf1<tm1.1(KOMP)Vlcg>/Pibf1<+>	C57BL/6N-Pibf1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757519	M	MP:0000063	decreased bone mineral density	Pink1<tm1b(EUCOMM)Wtsi>/Pink1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pink1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757519	M	MP:0010124	decreased bone mineral content	Pink1<tm1b(EUCOMM)Wtsi>/Pink1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pink1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757520	M	MP:0001402	decreased locomotor activity	Pipox<tm1b(EUCOMM)Wtsi>/Pipox<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pipox<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757522	F	MP:0001303	abnormal lens morphology	Pkd1l2<tm1b(KOMP)Mbp>/Pkd1l2<tm1b(KOMP)Mbp>	C57BL/6N-Pkd1l2<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5757522	F	MP:0001926	female infertility	Pkd1l2<tm1b(KOMP)Mbp>/Pkd1l2<tm1b(KOMP)Mbp>	C57BL/6N-Pkd1l2<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5757523	F	MP:0005565	increased blood urea nitrogen level	Pkd2l2<tm1b(EUCOMM)Wtsi>/Pkd2l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pkd2l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757523	M	MP:0013278	decreased fasting circulating glucose level	Pkd2l2<tm1b(EUCOMM)Wtsi>/Pkd2l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pkd2l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757523	M	MP:0000063	decreased bone mineral density	Pkd2l2<tm1b(EUCOMM)Wtsi>/Pkd2l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pkd2l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757523	F	MP:0005553	increased circulating creatinine level	Pkd2l2<tm1b(EUCOMM)Wtsi>/Pkd2l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pkd2l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757523	F	MP:0005627	increased circulating potassium level	Pkd2l2<tm1b(EUCOMM)Wtsi>/Pkd2l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pkd2l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757523	F	MP:0010087	increased circulating fructosamine level	Pkd2l2<tm1b(EUCOMM)Wtsi>/Pkd2l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pkd2l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757524	M	MP:0013278	decreased fasting circulating glucose level	Pkn1<tm1b(KOMP)Wtsi>/Pkn1<tm1b(KOMP)Wtsi>	C57BL/6N-Pkn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757524	M	MP:0000223	decreased monocyte cell number	Pkn1<tm1b(KOMP)Wtsi>/Pkn1<tm1b(KOMP)Wtsi>	C57BL/6N-Pkn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757524	M	MP:0005564	increased hemoglobin content	Pkn1<tm1b(KOMP)Wtsi>/Pkn1<tm1b(KOMP)Wtsi>	C57BL/6N-Pkn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757524	M	MP:0010024	increased total body fat amount	Pkn1<tm1b(KOMP)Wtsi>/Pkn1<tm1b(KOMP)Wtsi>	C57BL/6N-Pkn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757524	M	MP:0010068	decreased red blood cell distribution width	Pkn1<tm1b(KOMP)Wtsi>/Pkn1<tm1b(KOMP)Wtsi>	C57BL/6N-Pkn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757525	F	MP:0003233	prolonged QT interval	Pla2g10<tm1b(EUCOMM)Hmgu>/Pla2g10<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pla2g10<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757525	F	MP:0003928	increased heart rate variability	Pla2g10<tm1b(EUCOMM)Hmgu>/Pla2g10<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pla2g10<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757525	F	MP:0004156	abnormal QT variability	Pla2g10<tm1b(EUCOMM)Hmgu>/Pla2g10<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pla2g10<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757525	F	MP:0001304	cataract	Pla2g10<tm1b(EUCOMM)Hmgu>/Pla2g10<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pla2g10<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757525	M	MP:0010053	decreased grip strength	Pla2g10<tm1b(EUCOMM)Hmgu>/Pla2g10<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pla2g10<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757525	F	MP:0010506	prolonged RR interval	Pla2g10<tm1b(EUCOMM)Hmgu>/Pla2g10<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pla2g10<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757525	F	MP:0005385	cardiovascular system phenotype	Pla2g10<tm1b(EUCOMM)Hmgu>/Pla2g10<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pla2g10<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757525	F	MP:0005333	decreased heart rate	Pla2g10<tm1b(EUCOMM)Hmgu>/Pla2g10<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pla2g10<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757526	M	MP:0002591	decreased mean corpuscular volume	Plac9<tm1b(EUCOMM)Hmgu>/Plac9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plac9<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757526	M	MP:0010024	increased total body fat amount	Plac9<tm1b(EUCOMM)Hmgu>/Plac9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plac9<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757526	M	MP:0013278	decreased fasting circulating glucose level	Plac9<tm1b(EUCOMM)Hmgu>/Plac9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plac9<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757526	M	MP:0010068	decreased red blood cell distribution width	Plac9<tm1b(EUCOMM)Hmgu>/Plac9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plac9<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757526	M	MP:0003961	decreased lean body mass	Plac9<tm1b(EUCOMM)Hmgu>/Plac9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plac9<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757526	M	MP:0010087	increased circulating fructosamine level	Plac9<tm1b(EUCOMM)Hmgu>/Plac9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plac9<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757526	M	MP:0000222	decreased neutrophil cell number	Plac9<tm1b(EUCOMM)Hmgu>/Plac9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plac9<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757527	F	MP:0008935	decreased mean platelet volume	Pld5<tm1b(KOMP)Wtsi>/Pld5<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Pld5<tm1b(KOMP)Wtsi> Tyr<c-Brd>/Wtsi	N	MGI:5576271
MGI:5757527	F	MP:0004599	abnormal vertebral arch morphology	Pld5<tm1b(KOMP)Wtsi>/Pld5<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Pld5<tm1b(KOMP)Wtsi> Tyr<c-Brd>/Wtsi	N	MGI:5576271
MGI:5757527	M	MP:0010068	decreased red blood cell distribution width	Pld5<tm1b(KOMP)Wtsi>/Pld5<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Pld5<tm1b(KOMP)Wtsi> Tyr<c-Brd>/Wtsi	N	MGI:5576271
MGI:5757527	M	MP:0003961	decreased lean body mass	Pld5<tm1b(KOMP)Wtsi>/Pld5<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Pld5<tm1b(KOMP)Wtsi> Tyr<c-Brd>/Wtsi	N	MGI:5576271
MGI:5757527	F	MP:0001556	increased circulating HDL cholesterol level	Pld5<tm1b(KOMP)Wtsi>/Pld5<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Pld5<tm1b(KOMP)Wtsi> Tyr<c-Brd>/Wtsi	N	MGI:5576271
MGI:5757528	F	MP:0008528	polycystic kidney	Plekhm1<tm1b(EUCOMM)Hmgu>/Plekhm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plekhm1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757528	M	MP:0008259	abnormal optic disk morphology	Plekhm1<tm1b(EUCOMM)Hmgu>/Plekhm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plekhm1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757528	F	MP:0005343	increased circulating aspartate transaminase level	Plekhm1<tm1b(EUCOMM)Hmgu>/Plekhm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plekhm1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757528	M	MP:0000062	increased bone mineral density	Plekhm1<tm1b(EUCOMM)Hmgu>/Plekhm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plekhm1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757528	M	MP:0010123	increased bone mineral content	Plekhm1<tm1b(EUCOMM)Hmgu>/Plekhm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plekhm1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757528	F	MP:0002764	short tibia	Plekhm1<tm1b(EUCOMM)Hmgu>/Plekhm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plekhm1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757528	F	MP:0002941	increased circulating alanine transaminase level	Plekhm1<tm1b(EUCOMM)Hmgu>/Plekhm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plekhm1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757528	M	MP:0010025	decreased total body fat amount	Plekhm1<tm1b(EUCOMM)Hmgu>/Plekhm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plekhm1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757528	M	MP:0000137	abnormal vertebrae morphology	Plekhm1<tm1b(EUCOMM)Hmgu>/Plekhm1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plekhm1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757530	M	MP:0009142	decreased prepulse inhibition	Plod1<tm1b(EUCOMM)Hmgu>/Plod1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plod1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757531	F	MP:0005553	increased circulating creatinine level	Plpp3<tm1b(EUCOMM)Hmgu>/Plpp3<+>	C57BL/6N-Plpp3<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757531	F	MP:0005562	decreased mean corpuscular hemoglobin	Plpp3<tm1b(EUCOMM)Hmgu>/Plpp3<+>	C57BL/6N-Plpp3<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757533	M	MP:0001148	enlarged testis	Plpp6<tm1.1(KOMP)Vlcg>/Plpp6<tm1.1(KOMP)Vlcg>	C57BL/6N-Plpp6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757533	M	MP:0001146	abnormal testis morphology	Plpp6<tm1.1(KOMP)Vlcg>/Plpp6<tm1.1(KOMP)Vlcg>	C57BL/6N-Plpp6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757535	F	MP:0005565	increased blood urea nitrogen level	Pmm2<tm1b(EUCOMM)Hmgu>/Pmm2<+>	C57BL/6N-Pmm2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757535	M	MP:0000702	enlarged lymph nodes	Pmm2<tm1b(EUCOMM)Hmgu>/Pmm2<+>	C57BL/6N-Pmm2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757538	M	MP:0002079	increased circulating insulin level	Pold3<tm1b(EUCOMM)Wtsi>/Pold3<+>	C57BL/6N-Pold3<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757542	M	MP:0010123	increased bone mineral content	Postn<tm1.1(KOMP)Vlcg>/Postn<tm1.1(KOMP)Vlcg>	C57BL/6N-Postn<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757542	F	MP:0003795	abnormal bone structure	Postn<tm1.1(KOMP)Vlcg>/Postn<tm1.1(KOMP)Vlcg>	C57BL/6N-Postn<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757542	F	MP:0000063	decreased bone mineral density	Postn<tm1.1(KOMP)Vlcg>/Postn<tm1.1(KOMP)Vlcg>	C57BL/6N-Postn<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757542	F	MP:0001523	impaired righting response	Postn<tm1.1(KOMP)Vlcg>/Postn<tm1.1(KOMP)Vlcg>	C57BL/6N-Postn<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757542	M	MP:0005505	thrombocytosis	Postn<tm1.1(KOMP)Vlcg>/Postn<tm1.1(KOMP)Vlcg>	C57BL/6N-Postn<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757542	F	MP:0002968	increased circulating alkaline phosphatase level	Postn<tm1.1(KOMP)Vlcg>/Postn<tm1.1(KOMP)Vlcg>	C57BL/6N-Postn<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757542	F	MP:0020870	decreased thigmotaxis	Postn<tm1.1(KOMP)Vlcg>/Postn<tm1.1(KOMP)Vlcg>	C57BL/6N-Postn<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757542	F	MP:0010124	decreased bone mineral content	Postn<tm1.1(KOMP)Vlcg>/Postn<tm1.1(KOMP)Vlcg>	C57BL/6N-Postn<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757543	M	MP:0003961	decreased lean body mass	Pparg<tm1b(KOMP)Wtsi>/Pparg<+>	C57BL/6N-Pparg<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757543	F	MP:0001406	abnormal gait	Pparg<tm1b(KOMP)Wtsi>/Pparg<+>	C57BL/6N-Pparg<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757543	M	MP:0010024	increased total body fat amount	Pparg<tm1b(KOMP)Wtsi>/Pparg<+>	C57BL/6N-Pparg<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757545	M	MP:0005178	increased circulating cholesterol level	Ppil3<tm1b(EUCOMM)Wtsi>/Ppil3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ppil3<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757545	M	MP:0001554	increased circulating free fatty acids level	Ppil3<tm1b(EUCOMM)Wtsi>/Ppil3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ppil3<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757545	M	MP:0006358	absent pinna reflex	Ppil3<tm1b(EUCOMM)Wtsi>/Ppil3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ppil3<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757545	M	MP:0001556	increased circulating HDL cholesterol level	Ppil3<tm1b(EUCOMM)Wtsi>/Ppil3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ppil3<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757546	F	MP:0002764	short tibia	Ppm1a<tm1b(EUCOMM)Hmgu>/Ppm1a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppm1a<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757546	F	MP:0010124	decreased bone mineral content	Ppm1a<tm1b(EUCOMM)Hmgu>/Ppm1a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppm1a<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757546	F	MP:0010052	increased grip strength	Ppm1a<tm1b(EUCOMM)Hmgu>/Ppm1a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppm1a<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757546	M	MP:0001513	limb grasping	Ppm1a<tm1b(EUCOMM)Hmgu>/Ppm1a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppm1a<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757546	F	MP:0003795	abnormal bone structure	Ppm1a<tm1b(EUCOMM)Hmgu>/Ppm1a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppm1a<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757549	M	MP:0001925	male infertility	Ppp2r1b<tm1b(EUCOMM)Wtsi>/Ppp2r1b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ppp2r1b<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757549	F	MP:0013279	increased fasting circulating glucose level	Ppp2r1b<tm1b(EUCOMM)Wtsi>/Ppp2r1b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ppp2r1b<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757550	F	MP:0002968	increased circulating alkaline phosphatase level	Ppp2r3a<tm1(KOMP)Mbp>/Ppp2r3a<tm1(KOMP)Mbp>	C57BL/6N-Ppp2r3a<tm1(KOMP)Mbp>/Nju	N	MGI:5576271
MGI:5757551	F	MP:0002135	abnormal kidney morphology	Ppp4r2<tm2b(EUCOMM)Hmgu>/Ppp4r2<+>	C57BL/6N-Ppp4r2<tm2b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757551	M	MP:0001399	hyperactivity	Ppp4r2<tm2b(EUCOMM)Hmgu>/Ppp4r2<+>	C57BL/6N-Ppp4r2<tm2b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757553	M	MP:0002764	short tibia	Ppp6c<tm1b(EUCOMM)Hmgu>/Ppp6c<+>	C57BL/6N-Ppp6c<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757553	M	MP:0013279	increased fasting circulating glucose level	Ppp6c<tm1b(EUCOMM)Hmgu>/Ppp6c<+>	C57BL/6N-Ppp6c<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757553	F	MP:0001392	abnormal locomotor behavior	Ppp6c<tm1b(EUCOMM)Hmgu>/Ppp6c<+>	C57BL/6N-Ppp6c<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757555	M	MP:0003960	increased lean body mass	Prdm10<tm1b(EUCOMM)Hmgu>/Prdm10<+>	C57BL/6N-Prdm10<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757555	M	MP:0010124	decreased bone mineral content	Prdm10<tm1b(EUCOMM)Hmgu>/Prdm10<+>	C57BL/6N-Prdm10<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757555	M	MP:0010053	decreased grip strength	Prdm10<tm1b(EUCOMM)Hmgu>/Prdm10<+>	C57BL/6N-Prdm10<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757555	M	MP:0010025	decreased total body fat amount	Prdm10<tm1b(EUCOMM)Hmgu>/Prdm10<+>	C57BL/6N-Prdm10<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757557	F	MP:0010393	shortened QRS complex duration	Prdm12<tm2b(EUCOMM)Hmgu>/Prdm12<+>	C57BL/6N-Prdm12<tm2b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757557	M	MP:0001402	decreased locomotor activity	Prdm12<tm2b(EUCOMM)Hmgu>/Prdm12<+>	C57BL/6N-Prdm12<tm2b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757557	M	MP:0005178	increased circulating cholesterol level	Prdm12<tm2b(EUCOMM)Hmgu>/Prdm12<+>	C57BL/6N-Prdm12<tm2b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757558	F	MP:0001297	microphthalmia	Prdm4<tm1b(EUCOMM)Hmgu>/Prdm4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prdm4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757558	F	MP:0005599	increased cardiac muscle contractility	Prdm4<tm1b(EUCOMM)Hmgu>/Prdm4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prdm4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757558	F	MP:0005293	impaired glucose tolerance	Prdm4<tm1b(EUCOMM)Hmgu>/Prdm4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prdm4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757558	F	MP:0002953	thick ventricular wall	Prdm4<tm1b(EUCOMM)Hmgu>/Prdm4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prdm4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757558	M	MP:0003960	increased lean body mass	Prdm4<tm1b(EUCOMM)Hmgu>/Prdm4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prdm4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757558	F	MP:0003921	abnormal heart left ventricle morphology	Prdm4<tm1b(EUCOMM)Hmgu>/Prdm4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prdm4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757558	F	MP:0000690	absent spleen	Prdm4<tm1b(EUCOMM)Hmgu>/Prdm4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prdm4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757558	F	MP:0008806	increased circulating amylase level	Prdm4<tm1b(EUCOMM)Hmgu>/Prdm4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prdm4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757558	M	MP:0010025	decreased total body fat amount	Prdm4<tm1b(EUCOMM)Hmgu>/Prdm4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prdm4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757558	M	MP:0011874	enlarged urinary bladder	Prdm4<tm1b(EUCOMM)Hmgu>/Prdm4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prdm4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757558	F	MP:0001406	abnormal gait	Prdm4<tm1b(EUCOMM)Hmgu>/Prdm4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prdm4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757559	M	MP:0001325	abnormal retina morphology	Primpol<tm1b(EUCOMM)Wtsi>/Primpol<tm1b(EUCOMM)Wtsi>	C57BL/6N-Primpol<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757559	M	MP:0000745	tremors	Primpol<tm1b(EUCOMM)Wtsi>/Primpol<tm1b(EUCOMM)Wtsi>	C57BL/6N-Primpol<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757559	M	MP:0001925	male infertility	Primpol<tm1b(EUCOMM)Wtsi>/Primpol<tm1b(EUCOMM)Wtsi>	C57BL/6N-Primpol<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757560	M	MP:0010090	increased circulating creatine kinase level	Prkaa2<tm1b(EUCOMM)Hmgu>/Prkaa2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prkaa2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757560	M	MP:0000691	enlarged spleen	Prkaa2<tm1b(EUCOMM)Hmgu>/Prkaa2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prkaa2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757560	M	MP:0005343	increased circulating aspartate transaminase level	Prkaa2<tm1b(EUCOMM)Hmgu>/Prkaa2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prkaa2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757560	M	MP:0010088	decreased circulating fructosamine level	Prkaa2<tm1b(EUCOMM)Hmgu>/Prkaa2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prkaa2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757560	M	MP:0005419	decreased circulating serum albumin level	Prkaa2<tm1b(EUCOMM)Hmgu>/Prkaa2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prkaa2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757560	M	MP:0013278	decreased fasting circulating glucose level	Prkaa2<tm1b(EUCOMM)Hmgu>/Prkaa2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prkaa2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757560	M	MP:0002941	increased circulating alanine transaminase level	Prkaa2<tm1b(EUCOMM)Hmgu>/Prkaa2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prkaa2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757561	M	MP:0010097	abnormal retina blood vessel morphology	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<+>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757561	M	MP:0011965	decreased total retina thickness	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<+>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757561	F	MP:0001304	cataract	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<+>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757561	F	MP:0001303	abnormal lens morphology	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<+>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757561	F	MP:0000198	decreased circulating phosphate level	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<+>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757561	M	MP:0002792	abnormal retina vasculature morphology	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<+>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757562	M	MP:0000183	decreased circulating LDL cholesterol level	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757564	M	MP:0002135	abnormal kidney morphology	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757564	M	MP:0002631	abnormal epididymis morphology	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757564	M	MP:0004931	enlarged epididymis	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757564	M	MP:0004952	increased spleen weight	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757564	M	MP:0003068	enlarged kidney	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757565	F	MP:0004151	decreased circulating iron level	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757565	M	MP:0005293	impaired glucose tolerance	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757565	M	MP:0005016	decreased lymphocyte cell number	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757565	M	MP:0000219	increased neutrophil cell number	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757565	F	MP:0013279	increased fasting circulating glucose level	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757565	M	MP:0000186	decreased circulating HDL cholesterol level	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757565	M	MP:0005179	decreased circulating cholesterol level	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757566	F	MP:0005344	increased circulating bilirubin level	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757566	F	MP:0006353	increased glycosylated hemoglobin level	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757566	F	MP:0000063	decreased bone mineral density	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757566	F	MP:0010124	decreased bone mineral content	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757568	F	MP:0005011	increased eosinophil cell number	Prkab2<tm1b(EUCOMM)Hmgu>/Prkab2<+>	C57BL/6N-Prkab2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757568	M	MP:0008935	decreased mean platelet volume	Prkab2<tm1b(EUCOMM)Hmgu>/Prkab2<+>	C57BL/6N-Prkab2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757571	M	MP:0003961	decreased lean body mass	Prpf31<tm1a(EUCOMM)Wtsi>/Prpf31<+>	C57BL/6N-Prpf31<tm1a(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757571	M	MP:0010024	increased total body fat amount	Prpf31<tm1a(EUCOMM)Wtsi>/Prpf31<+>	C57BL/6N-Prpf31<tm1a(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757573	F	MP:0000195	decreased circulating calcium level	Prpf6<tm1.1(KOMP)Vlcg>/Prpf6<+>	C57BL/6N-Prpf6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757573	F	MP:0005561	increased mean corpuscular hemoglobin	Prpf6<tm1.1(KOMP)Vlcg>/Prpf6<+>	C57BL/6N-Prpf6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757573	M	MP:0001523	impaired righting response	Prpf6<tm1.1(KOMP)Vlcg>/Prpf6<+>	C57BL/6N-Prpf6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757575	F	MP:0000194	increased circulating calcium level	Prrg2<tm1b(EUCOMM)Wtsi>/Prrg2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Prrg2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757575	F	MP:0008810	increased circulating iron level	Prrg2<tm1b(EUCOMM)Wtsi>/Prrg2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Prrg2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757578	F	MP:0005385	cardiovascular system phenotype	Psph<tm1.1(KOMP)Vlcg>/Psph<+>	C57BL/6N-Psph<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757578	M	MP:0002768	small adrenal glands	Psph<tm1.1(KOMP)Vlcg>/Psph<+>	C57BL/6N-Psph<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757578	M	MP:0002644	decreased circulating triglyceride level	Psph<tm1.1(KOMP)Vlcg>/Psph<+>	C57BL/6N-Psph<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757578	F	MP:0003928	increased heart rate variability	Psph<tm1.1(KOMP)Vlcg>/Psph<+>	C57BL/6N-Psph<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757578	M	MP:0003179	thrombocytopenia	Psph<tm1.1(KOMP)Vlcg>/Psph<+>	C57BL/6N-Psph<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757582	M	MP:0001314	cornea opacity	Ptma<tm1.1(KOMP)Vlcg>/Ptma<+>	C57BL/6N-Ptma<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757582	M	MP:0001289	persistence of hyaloid vascular system	Ptma<tm1.1(KOMP)Vlcg>/Ptma<+>	C57BL/6N-Ptma<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757586	M	MP:0002968	increased circulating alkaline phosphatase level	Ptpn23<tm1b(EUCOMM)Hmgu>/Ptpn23<+>	C57BL/6N-Ptpn23<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757588	F	MP:0009142	decreased prepulse inhibition	Ptprv<tm1b(NCOM)Mfgc>/Ptprv<tm1b(NCOM)Mfgc>	C57BL/6N-Ptprv<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5757588	M	MP:0005628	decreased circulating potassium level	Ptprv<tm1b(NCOM)Mfgc>/Ptprv<tm1b(NCOM)Mfgc>	C57BL/6N-Ptprv<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5757590	M	MP:0000745	tremors	Pyroxd1<tm1b(KOMP)Wtsi>/Pyroxd1<+>	C57BL/6N-Pyroxd1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757590	M	MP:0000470	abnormal stomach morphology	Pyroxd1<tm1b(KOMP)Wtsi>/Pyroxd1<+>	C57BL/6N-Pyroxd1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757592	F	MP:0000195	decreased circulating calcium level	Rab19<tm1b(EUCOMM)Hmgu>/Rab19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rab19<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757592	F	MP:0001314	cornea opacity	Rab19<tm1b(EUCOMM)Hmgu>/Rab19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rab19<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757592	F	MP:0012361	decreased large unstained cell number	Rab19<tm1b(EUCOMM)Hmgu>/Rab19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rab19<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757592	F	MP:0005011	increased eosinophil cell number	Rab19<tm1b(EUCOMM)Hmgu>/Rab19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rab19<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757592	F	MP:0001469	abnormal contextual conditioning behavior	Rab19<tm1b(EUCOMM)Hmgu>/Rab19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rab19<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757592	F	MP:0001312	abnormal cornea morphology	Rab19<tm1b(EUCOMM)Hmgu>/Rab19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rab19<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757592	M	MP:0002833	increased heart weight	Rab19<tm1b(EUCOMM)Hmgu>/Rab19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rab19<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757592	F	MP:0011962	increased cornea thickness	Rab19<tm1b(EUCOMM)Hmgu>/Rab19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rab19<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757594	F	MP:0010124	decreased bone mineral content	Rab24<tm1.1(KOMP)Wtsi>/Rab24<tm1.1(KOMP)Wtsi>	C57BL/6N-Rab24<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757594	M	MP:0002833	increased heart weight	Rab24<tm1.1(KOMP)Wtsi>/Rab24<tm1.1(KOMP)Wtsi>	C57BL/6N-Rab24<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757594	F	MP:0003795	abnormal bone structure	Rab24<tm1.1(KOMP)Wtsi>/Rab24<tm1.1(KOMP)Wtsi>	C57BL/6N-Rab24<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757594	F	MP:0001258	decreased body length	Rab24<tm1.1(KOMP)Wtsi>/Rab24<tm1.1(KOMP)Wtsi>	C57BL/6N-Rab24<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757594	F	MP:0001510	abnormal coat appearance	Rab24<tm1.1(KOMP)Wtsi>/Rab24<tm1.1(KOMP)Wtsi>	C57BL/6N-Rab24<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757595	M	MP:0000274	enlarged heart	Rab32<tm1b(KOMP)Wtsi>/Rab32<tm1b(KOMP)Wtsi>	C57BL/6N-Rab32<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757595	F	MP:0009709	hydrometra	Rab32<tm1b(KOMP)Wtsi>/Rab32<tm1b(KOMP)Wtsi>	C57BL/6N-Rab32<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757595	M	MP:0000266	abnormal heart morphology	Rab32<tm1b(KOMP)Wtsi>/Rab32<tm1b(KOMP)Wtsi>	C57BL/6N-Rab32<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757595	M	MP:0003917	increased kidney weight	Rab32<tm1b(KOMP)Wtsi>/Rab32<tm1b(KOMP)Wtsi>	C57BL/6N-Rab32<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757596	F	MP:0005650	abnormal limb bud morphology	Rab34<tm1b(EUCOMM)Hmgu>/Rab34<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rab34<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757597	F	MP:0001304	cataract	Rab35<tm1b(EUCOMM)Hmgu>/Rab35<+>	C57BL/6N-Rab35<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757597	F	MP:0001303	abnormal lens morphology	Rab35<tm1b(EUCOMM)Hmgu>/Rab35<+>	C57BL/6N-Rab35<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757599	F	MP:0002968	increased circulating alkaline phosphatase level	Rab3ip<tm1.1(KOMP)Vlcg>/Rab3ip<tm1.1(KOMP)Vlcg>	C57BL/6N-Rab3ip<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757599	F	MP:0010124	decreased bone mineral content	Rab3ip<tm1.1(KOMP)Vlcg>/Rab3ip<tm1.1(KOMP)Vlcg>	C57BL/6N-Rab3ip<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757599	M	MP:0005561	increased mean corpuscular hemoglobin	Rab3ip<tm1.1(KOMP)Vlcg>/Rab3ip<tm1.1(KOMP)Vlcg>	C57BL/6N-Rab3ip<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757599	M	MP:0001417	decreased exploration in new environment	Rab3ip<tm1.1(KOMP)Vlcg>/Rab3ip<tm1.1(KOMP)Vlcg>	C57BL/6N-Rab3ip<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757599	M	MP:0003960	increased lean body mass	Rab3ip<tm1.1(KOMP)Vlcg>/Rab3ip<tm1.1(KOMP)Vlcg>	C57BL/6N-Rab3ip<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757599	F	MP:0003795	abnormal bone structure	Rab3ip<tm1.1(KOMP)Vlcg>/Rab3ip<tm1.1(KOMP)Vlcg>	C57BL/6N-Rab3ip<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757599	M	MP:0002590	increased mean corpuscular volume	Rab3ip<tm1.1(KOMP)Vlcg>/Rab3ip<tm1.1(KOMP)Vlcg>	C57BL/6N-Rab3ip<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757600	F	MP:0005562	decreased mean corpuscular hemoglobin	Rab40c<tm1b(KOMP)Wtsi>/Rab40c<+>	C57BL/6N-Rab40c<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757602	M	MP:0010053	decreased grip strength	Ramp1<tm1b(EUCOMM)Wtsi>/Ramp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ramp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757603	M	MP:0001556	increased circulating HDL cholesterol level	Rapsn<tm1b(EUCOMM)Wtsi>/Rapsn<+>	C57BL/6N-Rapsn<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757607	M	MP:0003019	increased circulating chloride level	Rbmx<tm2b(KOMP)Wtsi>/Y	C57BL/6N-Rbmx<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757607	M	MP:0000195	decreased circulating calcium level	Rbmx<tm2b(KOMP)Wtsi>/Y	C57BL/6N-Rbmx<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757607	M	MP:0010052	increased grip strength	Rbmx<tm2b(KOMP)Wtsi>/Y	C57BL/6N-Rbmx<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757608	F	MP:0002968	increased circulating alkaline phosphatase level	Rbmx<tm2b(KOMP)Wtsi>/Rbmx<tm2b(KOMP)Wtsi>	C57BL/6N-Rbmx<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757608	F	MP:0010052	increased grip strength	Rbmx<tm2b(KOMP)Wtsi>/Rbmx<tm2b(KOMP)Wtsi>	C57BL/6N-Rbmx<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757609	M	MP:0008806	increased circulating amylase level	Rbpjl<tm1b(KOMP)Wtsi>/Rbpjl<tm1b(KOMP)Wtsi>	C57BL/6N-Rbpjl<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757609	M	MP:0001410	head bobbing	Rbpjl<tm1b(KOMP)Wtsi>/Rbpjl<tm1b(KOMP)Wtsi>	C57BL/6N-Rbpjl<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757610	M	MP:0002591	decreased mean corpuscular volume	Rcc2<tm1b(EUCOMM)Wtsi>/Rcc2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rcc2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757610	M	MP:0008259	abnormal optic disk morphology	Rcc2<tm1b(EUCOMM)Wtsi>/Rcc2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rcc2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757610	F	MP:0002075	abnormal coat/hair pigmentation	Rcc2<tm1b(EUCOMM)Wtsi>/Rcc2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rcc2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757612	M	MP:0000745	tremors	Rel<tm1b(EUCOMM)Wtsi>/Rel<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rel<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757612	M	MP:0001284	absent vibrissae	Rel<tm1b(EUCOMM)Wtsi>/Rel<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rel<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757613	M	MP:0002833	increased heart weight	Resp18<tm1.1(KOMP)Vlcg>/Resp18<tm1.1(KOMP)Vlcg>	C57BL/6N-Resp18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757613	M	MP:0002702	decreased circulating free fatty acids level	Resp18<tm1.1(KOMP)Vlcg>/Resp18<tm1.1(KOMP)Vlcg>	C57BL/6N-Resp18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757616	M	MP:0005013	increased lymphocyte cell number	Rexo2<tm1b(EUCOMM)Wtsi>/Rexo2<+>	C57BL/6N-Rexo2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757616	M	MP:0013278	decreased fasting circulating glucose level	Rexo2<tm1b(EUCOMM)Wtsi>/Rexo2<+>	C57BL/6N-Rexo2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757616	M	MP:0002965	increased circulating serum albumin level	Rexo2<tm1b(EUCOMM)Wtsi>/Rexo2<+>	C57BL/6N-Rexo2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757616	M	MP:0001556	increased circulating HDL cholesterol level	Rexo2<tm1b(EUCOMM)Wtsi>/Rexo2<+>	C57BL/6N-Rexo2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757616	M	MP:0000222	decreased neutrophil cell number	Rexo2<tm1b(EUCOMM)Wtsi>/Rexo2<+>	C57BL/6N-Rexo2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757616	M	MP:0005178	increased circulating cholesterol level	Rexo2<tm1b(EUCOMM)Wtsi>/Rexo2<+>	C57BL/6N-Rexo2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757620	F	MP:0001402	decreased locomotor activity	Rfx7<tm2b(EUCOMM)Hmgu>/Rfx7<+>	C57BL/6N-Rfx7<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757620	F	MP:0001325	abnormal retina morphology	Rfx7<tm2b(EUCOMM)Hmgu>/Rfx7<+>	C57BL/6N-Rfx7<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757620	F	MP:0013278	decreased fasting circulating glucose level	Rfx7<tm2b(EUCOMM)Hmgu>/Rfx7<+>	C57BL/6N-Rfx7<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757622	F	MP:0000745	tremors	Rhbdl3<tm1b(EUCOMM)Wtsi>/Rhbdl3<+>	C57BL/6N-Rhbdl3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757624	M	MP:0000218	increased leukocyte cell number	Ric8b<tm1b(EUCOMM)Hmgu>/Ric8b<+>	C57BL/6N-Ric8b<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757624	M	MP:0005013	increased lymphocyte cell number	Ric8b<tm1b(EUCOMM)Hmgu>/Ric8b<+>	C57BL/6N-Ric8b<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757624	M	MP:0002606	increased basophil cell number	Ric8b<tm1b(EUCOMM)Hmgu>/Ric8b<+>	C57BL/6N-Ric8b<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757626	M	MP:0013279	increased fasting circulating glucose level	Rilpl1<tm1b(EUCOMM)Hmgu>/Rilpl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rilpl1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757628	M	MP:0003960	increased lean body mass	Rlbp1<tm1b(EUCOMM)Hmgu>/Rlbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rlbp1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757629	F	MP:0010124	decreased bone mineral content	Rln3<tm1(KOMP)Mbp>/Rln3<tm1(KOMP)Mbp>	C57BL/6N-Rln3<tm1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5757629	F	MP:0010024	increased total body fat amount	Rln3<tm1(KOMP)Mbp>/Rln3<tm1(KOMP)Mbp>	C57BL/6N-Rln3<tm1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5757629	F	MP:0008810	increased circulating iron level	Rln3<tm1(KOMP)Mbp>/Rln3<tm1(KOMP)Mbp>	C57BL/6N-Rln3<tm1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5757629	F	MP:0002874	decreased hemoglobin content	Rln3<tm1(KOMP)Mbp>/Rln3<tm1(KOMP)Mbp>	C57BL/6N-Rln3<tm1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5757629	F	MP:0002875	decreased erythrocyte cell number	Rln3<tm1(KOMP)Mbp>/Rln3<tm1(KOMP)Mbp>	C57BL/6N-Rln3<tm1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5757630	F	MP:0005278	abnormal cholesterol homeostasis	Carmil2<tm1b(KOMP)Mbp>/Carmil2<tm1b(KOMP)Mbp>	C57BL/6N-Carmil2<tm1b(KOMP)Mbp>/Orl	N	MGI:5576271
MGI:5757630	F	MP:0005559	increased circulating glucose level	Carmil2<tm1b(KOMP)Mbp>/Carmil2<tm1b(KOMP)Mbp>	C57BL/6N-Carmil2<tm1b(KOMP)Mbp>/Orl	N	MGI:5576271
MGI:5757631	M	MP:0005293	impaired glucose tolerance	Rnaset2b<tm1b(EUCOMM)Hmgu>/Rnaset2b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rnaset2b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757631	F	MP:0000691	enlarged spleen	Rnaset2b<tm1b(EUCOMM)Hmgu>/Rnaset2b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rnaset2b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757631	F	MP:0003068	enlarged kidney	Rnaset2b<tm1b(EUCOMM)Hmgu>/Rnaset2b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rnaset2b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757631	M	MP:0010052	increased grip strength	Rnaset2b<tm1b(EUCOMM)Hmgu>/Rnaset2b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rnaset2b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757632	M	MP:0005419	decreased circulating serum albumin level	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<+>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757632	M	MP:0010025	decreased total body fat amount	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<+>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757632	M	MP:0000274	enlarged heart	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<+>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757632	M	MP:0002833	increased heart weight	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<+>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757633	F	MP:0010052	increased grip strength	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<+>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757634	M	MP:0010053	decreased grip strength	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757634	F	MP:0000220	increased monocyte cell number	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757634	F	MP:0009142	decreased prepulse inhibition	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757634	F	MP:0005016	decreased lymphocyte cell number	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757634	M	MP:0005292	improved glucose tolerance	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757634	M	MP:0005419	decreased circulating serum albumin level	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757634	M	MP:0003900	shortened QT interval	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757634	M	MP:0001258	decreased body length	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757634	M	MP:0010571	shortened ST segment	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757635	M	MP:0001513	limb grasping	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757635	F	MP:0012362	increased large unstained cell number	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757635	F	MP:0002966	decreased circulating alkaline phosphatase level	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757635	M	MP:0001364	decreased anxiety-related response	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757635	F	MP:0004953	decreased spleen weight	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757635	F	MP:0009142	decreased prepulse inhibition	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757636	M	MP:0003960	increased lean body mass	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757636	F	MP:0000558	abnormal tibia morphology	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757636	M	MP:0010123	increased bone mineral content	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757636	F	MP:0001258	decreased body length	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757637	M	MP:0005560	decreased circulating glucose level	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757637	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757637	M	MP:0001399	hyperactivity	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757637	F	MP:0000947	convulsive seizures	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757637	M	MP:0013278	decreased fasting circulating glucose level	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757638	M	MP:0010123	increased bone mineral content	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757638	M	MP:0002591	decreased mean corpuscular volume	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757638	F	MP:0000063	decreased bone mineral density	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757639	F	MP:0004924	abnormal behavior	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757639	M	MP:0009142	decreased prepulse inhibition	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757639	F	MP:0000689	abnormal spleen morphology	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757639	F	MP:0002574	increased vertical activity	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757640	F	MP:0001552	increased circulating triglyceride level	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757640	F	MP:0005567	decreased circulating total protein level	Rnf10<tm1b(KOMP)Wtsi>/Rnf10<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757642	M	MP:0005178	increased circulating cholesterol level	Rnf144b<tm1b(EUCOMM)Hmgu>/Rnf144b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rnf144b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757642	M	MP:0000194	increased circulating calcium level	Rnf144b<tm1b(EUCOMM)Hmgu>/Rnf144b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rnf144b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757642	M	MP:0001529	abnormal vocalization	Rnf144b<tm1b(EUCOMM)Hmgu>/Rnf144b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rnf144b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757644	M	MP:0004924	abnormal behavior	Rnf20<tm1.1(KOMP)Vlcg>/Rnf20<+>	C57BL/6N-Rnf20<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5757644	M	MP:0020870	decreased thigmotaxis	Rnf20<tm1.1(KOMP)Vlcg>/Rnf20<+>	C57BL/6N-Rnf20<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5757644	M	MP:0001399	hyperactivity	Rnf20<tm1.1(KOMP)Vlcg>/Rnf20<+>	C57BL/6N-Rnf20<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5757646	M	MP:0001925	male infertility	Rnf216<tm1b(EUCOMM)Wtsi>/Rnf216<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rnf216<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757646	M	MP:0000220	increased monocyte cell number	Rnf216<tm1b(EUCOMM)Wtsi>/Rnf216<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rnf216<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757647	M	MP:0002590	increased mean corpuscular volume	Rnf25<tm1.1(KOMP)Vlcg>/Rnf25<tm1.1(KOMP)Vlcg>	C57BL/6N-Rnf25<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757647	M	MP:0003020	decreased circulating chloride level	Rnf25<tm1.1(KOMP)Vlcg>/Rnf25<tm1.1(KOMP)Vlcg>	C57BL/6N-Rnf25<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757647	F	MP:0001303	abnormal lens morphology	Rnf25<tm1.1(KOMP)Vlcg>/Rnf25<tm1.1(KOMP)Vlcg>	C57BL/6N-Rnf25<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757647	F	MP:0001523	impaired righting response	Rnf25<tm1.1(KOMP)Vlcg>/Rnf25<tm1.1(KOMP)Vlcg>	C57BL/6N-Rnf25<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757648	M	MP:0011965	decreased total retina thickness	Rnf38<tm1b(KOMP)Wtsi>/Rnf38<+>	C57BL/6N-Rnf38<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757648	M	MP:0010097	abnormal retina blood vessel morphology	Rnf38<tm1b(KOMP)Wtsi>/Rnf38<+>	C57BL/6N-Rnf38<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757651	M	MP:0004174	abnormal spine curvature	Ropn1l<tm1b(EUCOMM)Wtsi>/Ropn1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ropn1l<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757651	M	MP:0010053	decreased grip strength	Ropn1l<tm1b(EUCOMM)Wtsi>/Ropn1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ropn1l<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757651	M	MP:0000160	kyphosis	Ropn1l<tm1b(EUCOMM)Wtsi>/Ropn1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ropn1l<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757655	M	MP:0001566	increased circulating phosphate level	Rrm2<tm1b(KOMP)Wtsi>/Rrm2<+>	C57BL/6N-Rrm2<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757657	F	MP:0003984	embryonic growth retardation	Rrp8<tm1.1(KOMP)Vlcg>/Rrp8<tm1.1(KOMP)Vlcg>	C57BL/6N-Rrp8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757658	M	MP:0005566	decreased blood urea nitrogen level	Rsad1<tm1.1(KOMP)Vlcg>/Rsad1<+>	C57BL/6N-Rsad1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757658	M	MP:0000706	small thymus	Rsad1<tm1.1(KOMP)Vlcg>/Rsad1<+>	C57BL/6N-Rsad1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757658	F	MP:0001120	abnormal uterus morphology	Rsad1<tm1.1(KOMP)Vlcg>/Rsad1<+>	C57BL/6N-Rsad1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757659	M	MP:0000702	enlarged lymph nodes	Rsad1<tm1.1(KOMP)Vlcg>/Rsad1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rsad1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757659	M	MP:0002768	small adrenal glands	Rsad1<tm1.1(KOMP)Vlcg>/Rsad1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rsad1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757661	M	MP:0003961	decreased lean body mass	Rsbn1<tm1b(EUCOMM)Wtsi>/Rsbn1<+>	C57BL/6N-Rsbn1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757661	F	MP:0001392	abnormal locomotor behavior	Rsbn1<tm1b(EUCOMM)Wtsi>/Rsbn1<+>	C57BL/6N-Rsbn1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757661	M	MP:0002059	abnormal seminal vesicle morphology	Rsbn1<tm1b(EUCOMM)Wtsi>/Rsbn1<+>	C57BL/6N-Rsbn1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757661	M	MP:0005178	increased circulating cholesterol level	Rsbn1<tm1b(EUCOMM)Wtsi>/Rsbn1<+>	C57BL/6N-Rsbn1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757663	M	MP:0000062	increased bone mineral density	Rsf1<tm1b(EUCOMM)Wtsi>/Rsf1<+>	C57BL/6N-Rsf1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757663	F	MP:0009142	decreased prepulse inhibition	Rsf1<tm1b(EUCOMM)Wtsi>/Rsf1<+>	C57BL/6N-Rsf1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757665	F	MP:0001399	hyperactivity	Rsph9<tm1.1(KOMP)Vlcg>/Rsph9<+>	C57BL/6N-Rsph9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757665	F	MP:0004924	abnormal behavior	Rsph9<tm1.1(KOMP)Vlcg>/Rsph9<+>	C57BL/6N-Rsph9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757665	F	MP:0002797	increased thigmotaxis	Rsph9<tm1.1(KOMP)Vlcg>/Rsph9<+>	C57BL/6N-Rsph9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757669	M	MP:0010053	decreased grip strength	Rwdd3<tm1b(KOMP)Wtsi>/Rwdd3<+>	C57BL/6N-Rwdd3<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757671	F	MP:0002608	increased hematocrit	Rxfp2<tm1b(EUCOMM)Wtsi>/Rxfp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757671	M	MP:0000194	increased circulating calcium level	Rxfp2<tm1b(EUCOMM)Wtsi>/Rxfp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757671	M	MP:0001925	male infertility	Rxfp2<tm1b(EUCOMM)Wtsi>/Rxfp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757671	M	MP:0003233	prolonged QT interval	Rxfp2<tm1b(EUCOMM)Wtsi>/Rxfp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757671	M	MP:0008259	abnormal optic disk morphology	Rxfp2<tm1b(EUCOMM)Wtsi>/Rxfp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757671	M	MP:0001147	small testis	Rxfp2<tm1b(EUCOMM)Wtsi>/Rxfp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757671	M	MP:0011886	increased circulating lipase level	Rxfp2<tm1b(EUCOMM)Wtsi>/Rxfp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757671	M	MP:0005343	increased circulating aspartate transaminase level	Rxfp2<tm1b(EUCOMM)Wtsi>/Rxfp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757671	M	MP:0003928	increased heart rate variability	Rxfp2<tm1b(EUCOMM)Wtsi>/Rxfp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757671	F	MP:0005564	increased hemoglobin content	Rxfp2<tm1b(EUCOMM)Wtsi>/Rxfp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757671	M	MP:0000598	abnormal liver morphology	Rxfp2<tm1b(EUCOMM)Wtsi>/Rxfp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757671	F	MP:0003131	increased erythrocyte cell number	Rxfp2<tm1b(EUCOMM)Wtsi>/Rxfp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757671	M	MP:0009552	urinary bladder obstruction	Rxfp2<tm1b(EUCOMM)Wtsi>/Rxfp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757674	F	MP:0011100	preweaning lethality, complete penetrance	S100a14<tm1b(EUCOMM)Hmgu>/S100a14<tm1b(EUCOMM)Hmgu>	C57BL/6N-S100a14<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757675	F	MP:0001325	abnormal retina morphology	Sarnp<tm1b(EUCOMM)Hmgu>/Sarnp<+>	C57BL/6N-Sarnp<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757675	F	MP:0011965	decreased total retina thickness	Sarnp<tm1b(EUCOMM)Hmgu>/Sarnp<+>	C57BL/6N-Sarnp<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757675	M	MP:0001488	increased startle reflex	Sarnp<tm1b(EUCOMM)Hmgu>/Sarnp<+>	C57BL/6N-Sarnp<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757675	F	MP:0002699	abnormal vitreous body morphology	Sarnp<tm1b(EUCOMM)Hmgu>/Sarnp<+>	C57BL/6N-Sarnp<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757675	F	MP:0001303	abnormal lens morphology	Sarnp<tm1b(EUCOMM)Hmgu>/Sarnp<+>	C57BL/6N-Sarnp<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757676	F	MP:0001120	abnormal uterus morphology	Satb2<tm1b(KOMP)Wtsi>/Satb2<+>	C57BL/6N-Satb2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757678	F	MP:0004122	abnormal sinus arrhythmia	Scarb1<tm1b(EUCOMM)Wtsi>/Scarb1<+>	C57BL/6N-Scarb1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757678	M	MP:0010570	prolonged ST segment	Scarb1<tm1b(EUCOMM)Wtsi>/Scarb1<+>	C57BL/6N-Scarb1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757678	M	MP:0010506	prolonged RR interval	Scarb1<tm1b(EUCOMM)Wtsi>/Scarb1<+>	C57BL/6N-Scarb1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757679	M	MP:0002833	increased heart weight	Scarb1<tm1b(EUCOMM)Wtsi>/Scarb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Scarb1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757679	M	MP:0000691	enlarged spleen	Scarb1<tm1b(EUCOMM)Wtsi>/Scarb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Scarb1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757679	M	MP:0004952	increased spleen weight	Scarb1<tm1b(EUCOMM)Wtsi>/Scarb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Scarb1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757679	M	MP:0000274	enlarged heart	Scarb1<tm1b(EUCOMM)Wtsi>/Scarb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Scarb1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757679	M	MP:0002757	decreased vertical activity	Scarb1<tm1b(EUCOMM)Wtsi>/Scarb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Scarb1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757680	F	MP:0008935	decreased mean platelet volume	Scn4a<tm2b(KOMP)Wtsi>/Scn4a<+>	C57BL/6N-Scn4a<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757680	F	MP:0002966	decreased circulating alkaline phosphatase level	Scn4a<tm2b(KOMP)Wtsi>/Scn4a<+>	C57BL/6N-Scn4a<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757680	M	MP:0008806	increased circulating amylase level	Scn4a<tm2b(KOMP)Wtsi>/Scn4a<+>	C57BL/6N-Scn4a<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757682	F	MP:0010087	increased circulating fructosamine level	Scnn1b<tm1b(EUCOMM)Hmgu>/Scnn1b<+>	C57BL/6N-Scnn1b<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757682	F	MP:0004509	abnormal pelvic girdle bone morphology	Scnn1b<tm1b(EUCOMM)Hmgu>/Scnn1b<+>	C57BL/6N-Scnn1b<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757684	F	MP:0002075	abnormal coat/hair pigmentation	Sdc2<tm1b(KOMP)Wtsi>/Sdc2<tm1b(KOMP)Wtsi>	C57BL/6N-Sdc2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757684	M	MP:0001552	increased circulating triglyceride level	Sdc2<tm1b(KOMP)Wtsi>/Sdc2<tm1b(KOMP)Wtsi>	C57BL/6N-Sdc2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757684	M	MP:0010463	aorta stenosis	Sdc2<tm1b(KOMP)Wtsi>/Sdc2<tm1b(KOMP)Wtsi>	C57BL/6N-Sdc2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5757685	M	MP:0013279	increased fasting circulating glucose level	Sdhb<tm1b(EUCOMM)Hmgu>/Sdhb<+>	C57BL/6N-Sdhb<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757685	F	MP:0002135	abnormal kidney morphology	Sdhb<tm1b(EUCOMM)Hmgu>/Sdhb<+>	C57BL/6N-Sdhb<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757688	F	MP:0001325	abnormal retina morphology	Secisbp2<tm1c(EUCOMM)Wtsi>/Secisbp2<tm1c(EUCOMM)Wtsi>	C57BL/6N-Secisbp2<tm1a(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757688	M	MP:0000218	increased leukocyte cell number	Secisbp2<tm1c(EUCOMM)Wtsi>/Secisbp2<tm1c(EUCOMM)Wtsi>	C57BL/6N-Secisbp2<tm1a(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757690	M	MP:0004738	abnormal auditory brainstem response	Selenok<tm1b(EUCOMM)Wtsi>/Selenok<tm1b(EUCOMM)Wtsi>	C57BL/6N-Selenok<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757690	M	MP:0004174	abnormal spine curvature	Selenok<tm1b(EUCOMM)Wtsi>/Selenok<tm1b(EUCOMM)Wtsi>	C57BL/6N-Selenok<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757691	F	MP:0004222	iris synechia	Sema3f<tm1b(EUCOMM)Hmgu>/Sema3f<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sema3f<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757691	F	MP:0005419	decreased circulating serum albumin level	Sema3f<tm1b(EUCOMM)Hmgu>/Sema3f<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sema3f<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757691	M	MP:0001488	increased startle reflex	Sema3f<tm1b(EUCOMM)Hmgu>/Sema3f<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sema3f<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757691	M	MP:0001304	cataract	Sema3f<tm1b(EUCOMM)Hmgu>/Sema3f<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sema3f<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757691	F	MP:0008810	increased circulating iron level	Sema3f<tm1b(EUCOMM)Hmgu>/Sema3f<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sema3f<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757691	F	MP:0000745	tremors	Sema3f<tm1b(EUCOMM)Hmgu>/Sema3f<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sema3f<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757691	F	MP:0005567	decreased circulating total protein level	Sema3f<tm1b(EUCOMM)Hmgu>/Sema3f<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sema3f<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757691	F	MP:0001406	abnormal gait	Sema3f<tm1b(EUCOMM)Hmgu>/Sema3f<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sema3f<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757692	M	MP:0002968	increased circulating alkaline phosphatase level	Sema4d<tm1b(EUCOMM)Wtsi>/Sema4d<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sema4d<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757692	M	MP:0000274	enlarged heart	Sema4d<tm1b(EUCOMM)Wtsi>/Sema4d<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sema4d<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757692	F	MP:0000691	enlarged spleen	Sema4d<tm1b(EUCOMM)Wtsi>/Sema4d<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sema4d<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757693	F	MP:0002075	abnormal coat/hair pigmentation	Senp7<tm1b(EUCOMM)Hmgu>/Senp7<tm1b(EUCOMM)Hmgu>	C57BL/6N-Senp7<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757693	F	MP:0001488	increased startle reflex	Senp7<tm1b(EUCOMM)Hmgu>/Senp7<tm1b(EUCOMM)Hmgu>	C57BL/6N-Senp7<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757695	F	MP:0005178	increased circulating cholesterol level	Serpinb5<tm1b(KOMP)Wtsi>/Serpinb5<tm1b(KOMP)Wtsi>	C57BL/6N-Serpinb5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757695	F	MP:0011396	abnormal sleep behavior	Serpinb5<tm1b(KOMP)Wtsi>/Serpinb5<tm1b(KOMP)Wtsi>	C57BL/6N-Serpinb5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757696	M	MP:0001147	small testis	Setx<tm1b(EUCOMM)Wtsi>/Setx<tm1b(EUCOMM)Wtsi>	C57BL/6N-Setx<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757696	F	MP:0011965	decreased total retina thickness	Setx<tm1b(EUCOMM)Wtsi>/Setx<tm1b(EUCOMM)Wtsi>	C57BL/6N-Setx<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757696	F	MP:0005011	increased eosinophil cell number	Setx<tm1b(EUCOMM)Wtsi>/Setx<tm1b(EUCOMM)Wtsi>	C57BL/6N-Setx<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757696	F	MP:0000219	increased neutrophil cell number	Setx<tm1b(EUCOMM)Wtsi>/Setx<tm1b(EUCOMM)Wtsi>	C57BL/6N-Setx<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757696	M	MP:0001925	male infertility	Setx<tm1b(EUCOMM)Wtsi>/Setx<tm1b(EUCOMM)Wtsi>	C57BL/6N-Setx<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757696	M	MP:0005292	improved glucose tolerance	Setx<tm1b(EUCOMM)Wtsi>/Setx<tm1b(EUCOMM)Wtsi>	C57BL/6N-Setx<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757697	F	MP:0001406	abnormal gait	Sez6l<tm1b(EUCOMM)Hmgu>/Sez6l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sez6l<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757697	M	MP:0002968	increased circulating alkaline phosphatase level	Sez6l<tm1b(EUCOMM)Hmgu>/Sez6l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sez6l<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757697	M	MP:0005419	decreased circulating serum albumin level	Sez6l<tm1b(EUCOMM)Hmgu>/Sez6l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sez6l<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757697	M	MP:0010379	decreased respiratory quotient	Sez6l<tm1b(EUCOMM)Hmgu>/Sez6l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sez6l<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757698	M	MP:0000579	abnormal nail morphology	Sgip1<tm1b(EUCOMM)Hmgu>/Sgip1<+>	C57BL/6N-Sgip1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757698	M	MP:0011886	increased circulating lipase level	Sgip1<tm1b(EUCOMM)Hmgu>/Sgip1<+>	C57BL/6N-Sgip1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757698	M	MP:0002110	abnormal digit morphology	Sgip1<tm1b(EUCOMM)Hmgu>/Sgip1<+>	C57BL/6N-Sgip1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757698	F	MP:0010097	abnormal retina blood vessel morphology	Sgip1<tm1b(EUCOMM)Hmgu>/Sgip1<+>	C57BL/6N-Sgip1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757699	M	MP:0001399	hyperactivity	Sgip1<tm1b(EUCOMM)Hmgu>/Sgip1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sgip1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757700	F	MP:0008810	increased circulating iron level	Sgsm1<tm1b(EUCOMM)Wtsi>/Sgsm1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sgsm1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757700	M	MP:0010067	increased red blood cell distribution width	Sgsm1<tm1b(EUCOMM)Wtsi>/Sgsm1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sgsm1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757701	M	MP:0002764	short tibia	Sh3bp2<tm1b(KOMP)Wtsi>/Sh3bp2<tm1b(KOMP)Wtsi>	C57BL/6N-Sh3bp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757701	M	MP:0005343	increased circulating aspartate transaminase level	Sh3bp2<tm1b(KOMP)Wtsi>/Sh3bp2<tm1b(KOMP)Wtsi>	C57BL/6N-Sh3bp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757703	F	MP:0010124	decreased bone mineral content	Sh3gl2<tm1b(EUCOMM)Wtsi>/Sh3gl2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sh3gl2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757703	M	MP:0005343	increased circulating aspartate transaminase level	Sh3gl2<tm1b(EUCOMM)Wtsi>/Sh3gl2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sh3gl2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757703	F	MP:0010053	decreased grip strength	Sh3gl2<tm1b(EUCOMM)Wtsi>/Sh3gl2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sh3gl2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757703	M	MP:0002941	increased circulating alanine transaminase level	Sh3gl2<tm1b(EUCOMM)Wtsi>/Sh3gl2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sh3gl2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757704	F	MP:0002968	increased circulating alkaline phosphatase level	Sh3pxd2a<tm1b(EUCOMM)Wtsi>/Sh3pxd2a<+>	C57BL/6N-Sh3pxd2a<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757706	F	MP:0001556	increased circulating HDL cholesterol level	Shh<tm1b(EUCOMM)Wtsi>/Shh<+>	C57BL/6N-Shh<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757706	M	MP:0010124	decreased bone mineral content	Shh<tm1b(EUCOMM)Wtsi>/Shh<+>	C57BL/6N-Shh<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757706	M	MP:0005293	impaired glucose tolerance	Shh<tm1b(EUCOMM)Wtsi>/Shh<+>	C57BL/6N-Shh<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757706	M	MP:0010024	increased total body fat amount	Shh<tm1b(EUCOMM)Wtsi>/Shh<+>	C57BL/6N-Shh<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757706	M	MP:0003961	decreased lean body mass	Shh<tm1b(EUCOMM)Wtsi>/Shh<+>	C57BL/6N-Shh<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757708	F	MP:0004122	abnormal sinus arrhythmia	Sirt1<tm1b(EUCOMM)Wtsi>/Sirt1<+>	C57BL/6N-Sirt1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757709	M	MP:0005287	narrow eye opening	Sirt1<tm1b(EUCOMM)Wtsi>/Sirt1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sirt1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757709	M	MP:0000455	abnormal maxilla morphology	Sirt1<tm1b(EUCOMM)Wtsi>/Sirt1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sirt1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757709	M	MP:0001322	abnormal iris morphology	Sirt1<tm1b(EUCOMM)Wtsi>/Sirt1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sirt1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757709	M	MP:0002100	abnormal tooth morphology	Sirt1<tm1b(EUCOMM)Wtsi>/Sirt1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sirt1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757709	M	MP:0000443	abnormal snout morphology	Sirt1<tm1b(EUCOMM)Wtsi>/Sirt1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sirt1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757710	M	MP:0005568	increased circulating total protein level	Sirt4<tm1b(EUCOMM)Hmgu>/Sirt4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sirt4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757710	M	MP:0001406	abnormal gait	Sirt4<tm1b(EUCOMM)Hmgu>/Sirt4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sirt4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757710	M	MP:0002965	increased circulating serum albumin level	Sirt4<tm1b(EUCOMM)Hmgu>/Sirt4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sirt4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757710	F	MP:0001417	decreased exploration in new environment	Sirt4<tm1b(EUCOMM)Hmgu>/Sirt4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sirt4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757710	M	MP:0010087	increased circulating fructosamine level	Sirt4<tm1b(EUCOMM)Hmgu>/Sirt4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sirt4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757711	M	MP:0000709	enlarged thymus	Skida1<tm1.1(KOMP)Wtsi>/Skida1<+>	C57BL/6N-Skida1<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757712	M	MP:0000692	small spleen	Skida1<tm1.1(KOMP)Wtsi>/Skida1<tm1.1(KOMP)Wtsi>	C57BL/6N-Skida1<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757712	F	MP:0000709	enlarged thymus	Skida1<tm1.1(KOMP)Wtsi>/Skida1<tm1.1(KOMP)Wtsi>	C57BL/6N-Skida1<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757712	F	MP:0001120	abnormal uterus morphology	Skida1<tm1.1(KOMP)Wtsi>/Skida1<tm1.1(KOMP)Wtsi>	C57BL/6N-Skida1<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757713	F	MP:0002591	decreased mean corpuscular volume	Slc15a3<tm1b(KOMP)Wtsi>/Slc15a3<tm1b(KOMP)Wtsi>	C57BL/6N-Slc15a3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757713	M	MP:0000220	increased monocyte cell number	Slc15a3<tm1b(KOMP)Wtsi>/Slc15a3<tm1b(KOMP)Wtsi>	C57BL/6N-Slc15a3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757714	F	MP:0002792	abnormal retina vasculature morphology	Slc20a2<tm1b(EUCOMM)Wtsi>/Slc20a2<+>	C57BL/6N-Slc20a2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757714	F	MP:0001516	abnormal motor coordination/balance	Slc20a2<tm1b(EUCOMM)Wtsi>/Slc20a2<+>	C57BL/6N-Slc20a2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757714	F	MP:0001325	abnormal retina morphology	Slc20a2<tm1b(EUCOMM)Wtsi>/Slc20a2<+>	C57BL/6N-Slc20a2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757714	M	MP:0001529	abnormal vocalization	Slc20a2<tm1b(EUCOMM)Wtsi>/Slc20a2<+>	C57BL/6N-Slc20a2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757714	M	MP:0011965	decreased total retina thickness	Slc20a2<tm1b(EUCOMM)Wtsi>/Slc20a2<+>	C57BL/6N-Slc20a2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757714	F	MP:0010024	increased total body fat amount	Slc20a2<tm1b(EUCOMM)Wtsi>/Slc20a2<+>	C57BL/6N-Slc20a2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757716	M	MP:0005178	increased circulating cholesterol level	Slc24a4<tm1b(KOMP)Wtsi>/Slc24a4<+>	C57BL/6N-Slc24a4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757716	M	MP:0010068	decreased red blood cell distribution width	Slc24a4<tm1b(KOMP)Wtsi>/Slc24a4<+>	C57BL/6N-Slc24a4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757716	M	MP:0001556	increased circulating HDL cholesterol level	Slc24a4<tm1b(KOMP)Wtsi>/Slc24a4<+>	C57BL/6N-Slc24a4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757716	M	MP:0010087	increased circulating fructosamine level	Slc24a4<tm1b(KOMP)Wtsi>/Slc24a4<+>	C57BL/6N-Slc24a4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757716	F	MP:0000709	enlarged thymus	Slc24a4<tm1b(KOMP)Wtsi>/Slc24a4<+>	C57BL/6N-Slc24a4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757717	F	MP:0002968	increased circulating alkaline phosphatase level	Slc24a4<tm1b(KOMP)Wtsi>/Slc24a4<tm1b(KOMP)Wtsi>	C57BL/6N-Slc24a4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757717	F	MP:0009142	decreased prepulse inhibition	Slc24a4<tm1b(KOMP)Wtsi>/Slc24a4<tm1b(KOMP)Wtsi>	C57BL/6N-Slc24a4<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757718	F	MP:0001325	abnormal retina morphology	Slc24a5<tm1b(KOMP)Mbp>/Slc24a5<tm1b(KOMP)Mbp>	C57BL/6N-Slc24a5<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757718	F	MP:0001523	impaired righting response	Slc24a5<tm1b(KOMP)Mbp>/Slc24a5<tm1b(KOMP)Mbp>	C57BL/6N-Slc24a5<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757718	F	MP:0009142	decreased prepulse inhibition	Slc24a5<tm1b(KOMP)Mbp>/Slc24a5<tm1b(KOMP)Mbp>	C57BL/6N-Slc24a5<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757718	M	MP:0013278	decreased fasting circulating glucose level	Slc24a5<tm1b(KOMP)Mbp>/Slc24a5<tm1b(KOMP)Mbp>	C57BL/6N-Slc24a5<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5757719	F	MP:0010124	decreased bone mineral content	Slc25a21<tm1d(KOMP)Wtsi>/Slc25a21<tm1d(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Slc25a21<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757719	M	MP:0005562	decreased mean corpuscular hemoglobin	Slc25a21<tm1d(KOMP)Wtsi>/Slc25a21<tm1d(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Slc25a21<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757719	F	MP:0003961	decreased lean body mass	Slc25a21<tm1d(KOMP)Wtsi>/Slc25a21<tm1d(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Slc25a21<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757719	M	MP:0010093	decreased circulating magnesium level	Slc25a21<tm1d(KOMP)Wtsi>/Slc25a21<tm1d(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Slc25a21<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757719	F	MP:0010024	increased total body fat amount	Slc25a21<tm1d(KOMP)Wtsi>/Slc25a21<tm1d(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Slc25a21<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757721	M	MP:0013279	increased fasting circulating glucose level	Slc2a2<tm1b(KOMP)Wtsi>/Slc2a2<+>	C57BL/6N-Slc2a2<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757721	M	MP:0006353	increased glycosylated hemoglobin level	Slc2a2<tm1b(KOMP)Wtsi>/Slc2a2<+>	C57BL/6N-Slc2a2<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757723	F	MP:0000702	enlarged lymph nodes	Slc2a5<tm1b(EUCOMM)Wtsi>/Slc2a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc2a5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757723	F	MP:0000691	enlarged spleen	Slc2a5<tm1b(EUCOMM)Wtsi>/Slc2a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc2a5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757723	M	MP:0002059	abnormal seminal vesicle morphology	Slc2a5<tm1b(EUCOMM)Wtsi>/Slc2a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc2a5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757723	F	MP:0001417	decreased exploration in new environment	Slc2a5<tm1b(EUCOMM)Wtsi>/Slc2a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc2a5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757723	F	MP:0001126	abnormal ovary morphology	Slc2a5<tm1b(EUCOMM)Wtsi>/Slc2a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc2a5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757723	F	MP:0009709	hydrometra	Slc2a5<tm1b(EUCOMM)Wtsi>/Slc2a5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc2a5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757724	F	MP:0008810	increased circulating iron level	Slc38a10<tm1a(EUCOMM)Wtsi>/Slc38a10<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc38a10<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757724	M	MP:0001258	decreased body length	Slc38a10<tm1a(EUCOMM)Wtsi>/Slc38a10<tm1a(EUCOMM)Wtsi>	C57BL/6N-Slc38a10<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757725	M	MP:0001552	increased circulating triglyceride level	Slc39a8<tm1b(EUCOMM)Wtsi>/Slc39a8<+>	C57BL/6N-Slc39a8<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:5757727	M	MP:0000063	decreased bone mineral density	Slc40a1<tm1b(EUCOMM)Hmgu>/Slc40a1<+>	C57BL/6N-Slc40a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757727	M	MP:0001552	increased circulating triglyceride level	Slc40a1<tm1b(EUCOMM)Hmgu>/Slc40a1<+>	C57BL/6N-Slc40a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757727	M	MP:0003961	decreased lean body mass	Slc40a1<tm1b(EUCOMM)Hmgu>/Slc40a1<+>	C57BL/6N-Slc40a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757727	M	MP:0010024	increased total body fat amount	Slc40a1<tm1b(EUCOMM)Hmgu>/Slc40a1<+>	C57BL/6N-Slc40a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757727	M	MP:0010124	decreased bone mineral content	Slc40a1<tm1b(EUCOMM)Hmgu>/Slc40a1<+>	C57BL/6N-Slc40a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757729	M	MP:0001556	increased circulating HDL cholesterol level	Slc46a3<tm1.1(KOMP)Vlcg>/Slc46a3<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc46a3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757729	M	MP:0005505	thrombocytosis	Slc46a3<tm1.1(KOMP)Vlcg>/Slc46a3<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc46a3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757729	M	MP:0001417	decreased exploration in new environment	Slc46a3<tm1.1(KOMP)Vlcg>/Slc46a3<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc46a3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757729	M	MP:0005178	increased circulating cholesterol level	Slc46a3<tm1.1(KOMP)Vlcg>/Slc46a3<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc46a3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757729	M	MP:0001510	abnormal coat appearance	Slc46a3<tm1.1(KOMP)Vlcg>/Slc46a3<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc46a3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757730	M	MP:0010025	decreased total body fat amount	Slc52a2<tm1.1(KOMP)Vlcg>/Slc52a2<+>	C57BL/6N-Slc52a2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757730	M	MP:0001284	absent vibrissae	Slc52a2<tm1.1(KOMP)Vlcg>/Slc52a2<+>	C57BL/6N-Slc52a2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757730	M	MP:0002768	small adrenal glands	Slc52a2<tm1.1(KOMP)Vlcg>/Slc52a2<+>	C57BL/6N-Slc52a2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757732	M	MP:0002702	decreased circulating free fatty acids level	Slc6a3<tm1b(KOMP)Wtsi>/Slc6a3<+>	C57BL/6N-Slc6a3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757732	M	MP:0002833	increased heart weight	Slc6a3<tm1b(KOMP)Wtsi>/Slc6a3<+>	C57BL/6N-Slc6a3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757733	F	MP:0008259	abnormal optic disk morphology	Slc7a11<tm1b(EUCOMM)Wtsi>/Slc7a11<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc7a11<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757733	M	MP:0005559	increased circulating glucose level	Slc7a11<tm1b(EUCOMM)Wtsi>/Slc7a11<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc7a11<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757734	M	MP:0001258	decreased body length	Slc7a13<tm1.1(KOMP)Vlcg>/Slc7a13<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc7a13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757735	F	MP:0002968	increased circulating alkaline phosphatase level	Slc8a3<tm1.1(KOMP)Vlcg>/Slc8a3<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc8a3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757736	F	MP:0005178	increased circulating cholesterol level	Slc9a4<tm1b(EUCOMM)Wtsi>/Slc9a4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc9a4<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757737	M	MP:0000194	increased circulating calcium level	Slitrk4<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Slitrk4<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757738	M	MP:0005344	increased circulating bilirubin level	Smc5<tm1b(KOMP)Wtsi>/Smc5<+>	C57BL/6N-Smc5<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757738	M	MP:0000219	increased neutrophil cell number	Smc5<tm1b(KOMP)Wtsi>/Smc5<+>	C57BL/6N-Smc5<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757738	F	MP:0000745	tremors	Smc5<tm1b(KOMP)Wtsi>/Smc5<+>	C57BL/6N-Smc5<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757738	M	MP:0002875	decreased erythrocyte cell number	Smc5<tm1b(KOMP)Wtsi>/Smc5<+>	C57BL/6N-Smc5<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757738	M	MP:0003179	thrombocytopenia	Smc5<tm1b(KOMP)Wtsi>/Smc5<+>	C57BL/6N-Smc5<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757738	M	MP:0005011	increased eosinophil cell number	Smc5<tm1b(KOMP)Wtsi>/Smc5<+>	C57BL/6N-Smc5<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757738	M	MP:0005560	decreased circulating glucose level	Smc5<tm1b(KOMP)Wtsi>/Smc5<+>	C57BL/6N-Smc5<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757738	M	MP:0000186	decreased circulating HDL cholesterol level	Smc5<tm1b(KOMP)Wtsi>/Smc5<+>	C57BL/6N-Smc5<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757738	M	MP:0005016	decreased lymphocyte cell number	Smc5<tm1b(KOMP)Wtsi>/Smc5<+>	C57BL/6N-Smc5<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757738	M	MP:0005179	decreased circulating cholesterol level	Smc5<tm1b(KOMP)Wtsi>/Smc5<+>	C57BL/6N-Smc5<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5757742	F	MP:0002764	short tibia	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757742	F	MP:0005287	narrow eye opening	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757742	F	MP:0010097	abnormal retina blood vessel morphology	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757742	M	MP:0001325	abnormal retina morphology	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757742	F	MP:0006243	impaired pupillary reflex	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757742	F	MP:0002546	mydriasis	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757742	F	MP:0005016	decreased lymphocyte cell number	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757742	F	MP:0011496	abnormal head size	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757742	F	MP:0004509	abnormal pelvic girdle bone morphology	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757742	F	MP:0000219	increased neutrophil cell number	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757742	M	MP:0002792	abnormal retina vasculature morphology	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757743	M	MP:0002060	abnormal skin morphology	Smo<tm1b(KOMP)Wtsi>/Smo<+>	C57BL/6N-Smo<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757743	F	MP:0003928	increased heart rate variability	Smo<tm1b(KOMP)Wtsi>/Smo<+>	C57BL/6N-Smo<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757745	M	MP:0001925	male infertility	Smpd4<tm2b(KOMP)Wtsi>/Smpd4<tm2b(KOMP)Wtsi>	C57BL/6N-Smpd4<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757749	F	MP:0006243	impaired pupillary reflex	Snrnp200<tm1b(KOMP)Mbp>/Snrnp200<+>	C57BL/6N-Snrnp200<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5757749	F	MP:0002750	exophthalmos	Snrnp200<tm1b(KOMP)Mbp>/Snrnp200<+>	C57BL/6N-Snrnp200<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5757749	F	MP:0000220	increased monocyte cell number	Snrnp200<tm1b(KOMP)Mbp>/Snrnp200<+>	C57BL/6N-Snrnp200<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5757749	M	MP:0000274	enlarged heart	Snrnp200<tm1b(KOMP)Mbp>/Snrnp200<+>	C57BL/6N-Snrnp200<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5757751	M	MP:0000467	abnormal esophagus morphology	Snrnp27<tm1b(EUCOMM)Wtsi>/Snrnp27<+>	C57BL/6N-Snrnp27<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757751	M	MP:0013278	decreased fasting circulating glucose level	Snrnp27<tm1b(EUCOMM)Wtsi>/Snrnp27<+>	C57BL/6N-Snrnp27<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757751	F	MP:0001399	hyperactivity	Snrnp27<tm1b(EUCOMM)Wtsi>/Snrnp27<+>	C57BL/6N-Snrnp27<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757753	M	MP:0005178	increased circulating cholesterol level	Snx15<tm1.1(KOMP)Vlcg>/Snx15<tm1.1(KOMP)Vlcg>	C57BL/6N-Snx15<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757753	F	MP:0005560	decreased circulating glucose level	Snx15<tm1.1(KOMP)Vlcg>/Snx15<tm1.1(KOMP)Vlcg>	C57BL/6N-Snx15<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757753	F	MP:0001363	increased anxiety-related response	Snx15<tm1.1(KOMP)Vlcg>/Snx15<tm1.1(KOMP)Vlcg>	C57BL/6N-Snx15<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757753	M	MP:0001556	increased circulating HDL cholesterol level	Snx15<tm1.1(KOMP)Vlcg>/Snx15<tm1.1(KOMP)Vlcg>	C57BL/6N-Snx15<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757754	F	MP:0001120	abnormal uterus morphology	Snx22<tm1.1(KOMP)Wtsi>/Snx22<tm1.1(KOMP)Wtsi>	C57BL/6N-Snx22<tm1.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757754	F	MP:0001399	hyperactivity	Snx22<tm1.1(KOMP)Wtsi>/Snx22<tm1.1(KOMP)Wtsi>	C57BL/6N-Snx22<tm1.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757754	M	MP:0011110	preweaning lethality, incomplete penetrance	Snx22<tm1.1(KOMP)Wtsi>/Snx22<tm1.1(KOMP)Wtsi>	C57BL/6N-Snx22<tm1.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757761	M	MP:0003960	increased lean body mass	Spink14<tm1e(KOMP)Wtsi>/Spink14<tm1e(KOMP)Wtsi>	C57BL/6N-Spink14<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757762	F	MP:0005561	increased mean corpuscular hemoglobin	Spns2<tm1b(KOMP)Wtsi>/Spns2<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Spns2<tm1b(KOMP)Wtsi>/WtsiH	N	MGI:5576271
MGI:5757762	M	MP:0010124	decreased bone mineral content	Spns2<tm1b(KOMP)Wtsi>/Spns2<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Spns2<tm1b(KOMP)Wtsi>/WtsiH	N	MGI:5576271
MGI:5757762	F	MP:0001322	abnormal iris morphology	Spns2<tm1b(KOMP)Wtsi>/Spns2<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Spns2<tm1b(KOMP)Wtsi>/WtsiH	N	MGI:5576271
MGI:5757763	M	MP:0005343	increased circulating aspartate transaminase level	Spop<tm1b(KOMP)Wtsi>/Spop<+>	C57BL/6N-Spop<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757763	M	MP:0011940	decreased food intake	Spop<tm1b(KOMP)Wtsi>/Spop<+>	C57BL/6N-Spop<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757763	M	MP:0002768	small adrenal glands	Spop<tm1b(KOMP)Wtsi>/Spop<+>	C57BL/6N-Spop<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757763	M	MP:0000702	enlarged lymph nodes	Spop<tm1b(KOMP)Wtsi>/Spop<+>	C57BL/6N-Spop<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757763	M	MP:0010379	decreased respiratory quotient	Spop<tm1b(KOMP)Wtsi>/Spop<+>	C57BL/6N-Spop<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757763	F	MP:0010053	decreased grip strength	Spop<tm1b(KOMP)Wtsi>/Spop<+>	C57BL/6N-Spop<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757763	M	MP:0000706	small thymus	Spop<tm1b(KOMP)Wtsi>/Spop<+>	C57BL/6N-Spop<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757765	M	MP:0010090	increased circulating creatine kinase level	Sptbn2<tm1b(EUCOMM)Hmgu>/Sptbn2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sptbn2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757765	F	MP:0002874	decreased hemoglobin content	Sptbn2<tm1b(EUCOMM)Hmgu>/Sptbn2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sptbn2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757765	M	MP:0001566	increased circulating phosphate level	Sptbn2<tm1b(EUCOMM)Hmgu>/Sptbn2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sptbn2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757765	M	MP:0002764	short tibia	Sptbn2<tm1b(EUCOMM)Hmgu>/Sptbn2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sptbn2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757766	F	MP:0010124	decreased bone mineral content	Sra1<tm1b(EUCOMM)Hmgu>/Sra1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sra1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757766	F	MP:0003795	abnormal bone structure	Sra1<tm1b(EUCOMM)Hmgu>/Sra1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sra1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757766	F	MP:0001120	abnormal uterus morphology	Sra1<tm1b(EUCOMM)Hmgu>/Sra1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sra1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757766	M	MP:0000438	abnormal cranium morphology	Sra1<tm1b(EUCOMM)Hmgu>/Sra1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sra1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757766	F	MP:0008259	abnormal optic disk morphology	Sra1<tm1b(EUCOMM)Hmgu>/Sra1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sra1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757766	F	MP:0002989	small kidney	Sra1<tm1b(EUCOMM)Hmgu>/Sra1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sra1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757768	F	MP:0005343	increased circulating aspartate transaminase level	Srp9<tm1.1(KOMP)Vlcg>/Srp9<+>	C57BL/6N-Srp9<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757768	M	MP:0003019	increased circulating chloride level	Srp9<tm1.1(KOMP)Vlcg>/Srp9<+>	C57BL/6N-Srp9<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757770	M	MP:0006243	impaired pupillary reflex	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757770	M	MP:0003960	increased lean body mass	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757770	M	MP:0002833	increased heart weight	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757770	F	MP:0002092	abnormal eye morphology	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757770	F	MP:0001258	decreased body length	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757770	M	MP:0001488	increased startle reflex	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757770	M	MP:0010025	decreased total body fat amount	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757770	M	MP:0004931	enlarged epididymis	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757770	M	MP:0000266	abnormal heart morphology	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757770	M	MP:0002631	abnormal epididymis morphology	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757770	M	MP:0003402	decreased liver weight	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757770	M	MP:0001399	hyperactivity	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757770	M	MP:0002175	decreased brain weight	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757770	M	MP:0000274	enlarged heart	Ssbp2<tm1b(KOMP)Wtsi>/Ssbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Ssbp2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757772	M	MP:0003961	decreased lean body mass	Sst<tm1b(KOMP)Wtsi>/Sst<tm1b(KOMP)Wtsi>	C57BL/6N-Sst<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757772	M	MP:0008810	increased circulating iron level	Sst<tm1b(KOMP)Wtsi>/Sst<tm1b(KOMP)Wtsi>	C57BL/6N-Sst<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757772	M	MP:0010024	increased total body fat amount	Sst<tm1b(KOMP)Wtsi>/Sst<tm1b(KOMP)Wtsi>	C57BL/6N-Sst<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757772	M	MP:0010124	decreased bone mineral content	Sst<tm1b(KOMP)Wtsi>/Sst<tm1b(KOMP)Wtsi>	C57BL/6N-Sst<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757772	M	MP:0002965	increased circulating serum albumin level	Sst<tm1b(KOMP)Wtsi>/Sst<tm1b(KOMP)Wtsi>	C57BL/6N-Sst<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5757773	F	MP:0003961	decreased lean body mass	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	C57BL/6N-Stag3<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757773	F	MP:0010124	decreased bone mineral content	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	C57BL/6N-Stag3<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757773	F	MP:0005568	increased circulating total protein level	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	C57BL/6N-Stag3<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757773	F	MP:0010024	increased total body fat amount	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	C57BL/6N-Stag3<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757773	F	MP:0003795	abnormal bone structure	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	C57BL/6N-Stag3<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757773	F	MP:0010053	decreased grip strength	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	C57BL/6N-Stag3<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757773	F	MP:0001926	female infertility	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	C57BL/6N-Stag3<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757773	F	MP:0000063	decreased bone mineral density	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	C57BL/6N-Stag3<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757773	M	MP:0001925	male infertility	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	C57BL/6N-Stag3<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757773	M	MP:0001147	small testis	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	C57BL/6N-Stag3<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757773	F	MP:0013279	increased fasting circulating glucose level	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	C57BL/6N-Stag3<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757774	M	MP:0001402	decreased locomotor activity	Stard10<tm1b(KOMP)Wtsi>/Stard10<tm1b(KOMP)Wtsi>	C57BL/6N-Stard10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757775	M	MP:0005560	decreased circulating glucose level	Stx19<tm1.1(KOMP)Vlcg>/Stx19<tm1.1(KOMP)Vlcg>	C57BL/6N-Stx19<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757775	F	MP:0001510	abnormal coat appearance	Stx19<tm1.1(KOMP)Vlcg>/Stx19<tm1.1(KOMP)Vlcg>	C57BL/6N-Stx19<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757775	F	MP:0013279	increased fasting circulating glucose level	Stx19<tm1.1(KOMP)Vlcg>/Stx19<tm1.1(KOMP)Vlcg>	C57BL/6N-Stx19<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757777	F	MP:0005565	increased blood urea nitrogen level	Sult1c1<tm1b(KOMP)Wtsi>/Sult1c1<tm1b(KOMP)Wtsi>	C57BL/6N-Sult1c1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757779	F	MP:0005634	decreased circulating sodium level	Svep1<tm1b(EUCOMM)Hmgu>/Svep1<+>	C57BL/6N-Svep1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757779	F	MP:0000198	decreased circulating phosphate level	Svep1<tm1b(EUCOMM)Hmgu>/Svep1<+>	C57BL/6N-Svep1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757779	F	MP:0005564	increased hemoglobin content	Svep1<tm1b(EUCOMM)Hmgu>/Svep1<+>	C57BL/6N-Svep1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757779	M	MP:0010392	prolonged QRS complex duration	Svep1<tm1b(EUCOMM)Hmgu>/Svep1<+>	C57BL/6N-Svep1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757779	M	MP:0003131	increased erythrocyte cell number	Svep1<tm1b(EUCOMM)Hmgu>/Svep1<+>	C57BL/6N-Svep1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757779	M	MP:0005560	decreased circulating glucose level	Svep1<tm1b(EUCOMM)Hmgu>/Svep1<+>	C57BL/6N-Svep1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757779	M	MP:0002608	increased hematocrit	Svep1<tm1b(EUCOMM)Hmgu>/Svep1<+>	C57BL/6N-Svep1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757780	M	MP:0002109	abnormal limb morphology	Svep1<tm1b(EUCOMM)Hmgu>/Svep1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Svep1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757781	F	MP:0001399	hyperactivity	Syn3<tm1.1(KOMP)Vlcg>/Syn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Syn3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757781	F	MP:0020870	decreased thigmotaxis	Syn3<tm1.1(KOMP)Vlcg>/Syn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Syn3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757781	F	MP:0002875	decreased erythrocyte cell number	Syn3<tm1.1(KOMP)Vlcg>/Syn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Syn3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757781	F	MP:0000208	decreased hematocrit	Syn3<tm1.1(KOMP)Vlcg>/Syn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Syn3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757781	F	MP:0002874	decreased hemoglobin content	Syn3<tm1.1(KOMP)Vlcg>/Syn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Syn3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757781	F	MP:0002941	increased circulating alanine transaminase level	Syn3<tm1.1(KOMP)Vlcg>/Syn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Syn3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757781	M	MP:0001516	abnormal motor coordination/balance	Syn3<tm1.1(KOMP)Vlcg>/Syn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Syn3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757782	F	MP:0000745	tremors	Synj1<tm1b(EUCOMM)Wtsi>/Synj1<+>	C57BL/6N-Synj1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757782	M	MP:0000222	decreased neutrophil cell number	Synj1<tm1b(EUCOMM)Wtsi>/Synj1<+>	C57BL/6N-Synj1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757782	M	MP:0000223	decreased monocyte cell number	Synj1<tm1b(EUCOMM)Wtsi>/Synj1<+>	C57BL/6N-Synj1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757782	M	MP:0010068	decreased red blood cell distribution width	Synj1<tm1b(EUCOMM)Wtsi>/Synj1<+>	C57BL/6N-Synj1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757782	M	MP:0005013	increased lymphocyte cell number	Synj1<tm1b(EUCOMM)Wtsi>/Synj1<+>	C57BL/6N-Synj1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757785	M	MP:0001925	male infertility	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757785	F	MP:0001417	decreased exploration in new environment	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5757787	F	MP:0002092	abnormal eye morphology	Tango6<tm1b(EUCOMM)Hmgu>/Tango6<+>	C57BL/6N-Tango6<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757789	M	MP:0011239	abnormal skin coloration	Tbccd1<tm1b(EUCOMM)Hmgu>/Tbccd1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tbccd1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5757789	F	MP:0001926	female infertility	Tbccd1<tm1b(EUCOMM)Hmgu>/Tbccd1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tbccd1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5757789	M	MP:0001925	male infertility	Tbccd1<tm1b(EUCOMM)Hmgu>/Tbccd1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tbccd1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5757789	F	MP:0005293	impaired glucose tolerance	Tbccd1<tm1b(EUCOMM)Hmgu>/Tbccd1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tbccd1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5757791	M	MP:0005016	decreased lymphocyte cell number	Tcaim<tm1b(EUCOMM)Wtsi>/Tcaim<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tcaim<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757791	M	MP:0000219	increased neutrophil cell number	Tcaim<tm1b(EUCOMM)Wtsi>/Tcaim<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tcaim<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757793	F	MP:0002135	abnormal kidney morphology	Tdrp<tm1.1(KOMP)Vlcg>/Tdrp<tm1.1(KOMP)Vlcg>	C57BL/6N-Tdrp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757793	M	MP:0002631	abnormal epididymis morphology	Tdrp<tm1.1(KOMP)Vlcg>/Tdrp<tm1.1(KOMP)Vlcg>	C57BL/6N-Tdrp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757793	M	MP:0004931	enlarged epididymis	Tdrp<tm1.1(KOMP)Vlcg>/Tdrp<tm1.1(KOMP)Vlcg>	C57BL/6N-Tdrp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757793	F	MP:0001120	abnormal uterus morphology	Tdrp<tm1.1(KOMP)Vlcg>/Tdrp<tm1.1(KOMP)Vlcg>	C57BL/6N-Tdrp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757793	F	MP:0008528	polycystic kidney	Tdrp<tm1.1(KOMP)Vlcg>/Tdrp<tm1.1(KOMP)Vlcg>	C57BL/6N-Tdrp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757794	M	MP:0005543	decreased cornea thickness	Tead1<tm1a(KOMP)Wtsi>/Tead1<+>	C57BL/6N-Tead1<tm1a(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757794	F	MP:0001325	abnormal retina morphology	Tead1<tm1a(KOMP)Wtsi>/Tead1<+>	C57BL/6N-Tead1<tm1a(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757796	F	MP:0011960	abnormal eye anterior chamber depth	Tead1<tm1b(KOMP)Wtsi>/Tead1<+>	C57BL/6N-Tead1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757796	F	MP:0010024	increased total body fat amount	Tead1<tm1b(KOMP)Wtsi>/Tead1<+>	C57BL/6N-Tead1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757796	F	MP:0009142	decreased prepulse inhibition	Tead1<tm1b(KOMP)Wtsi>/Tead1<+>	C57BL/6N-Tead1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757796	F	MP:0005293	impaired glucose tolerance	Tead1<tm1b(KOMP)Wtsi>/Tead1<+>	C57BL/6N-Tead1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757796	F	MP:0002100	abnormal tooth morphology	Tead1<tm1b(KOMP)Wtsi>/Tead1<+>	C57BL/6N-Tead1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757797	F	MP:0001697	abnormal embryo size	Tead1<tm1b(KOMP)Wtsi>/Tead1<tm1b(KOMP)Wtsi>	C57BL/6N-Tead1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757797	F	MP:0001700	abnormal embryo turning	Tead1<tm1b(KOMP)Wtsi>/Tead1<tm1b(KOMP)Wtsi>	C57BL/6N-Tead1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757798	M	MP:0003960	increased lean body mass	Tfeb<tm1a(EUCOMM)Wtsi>/Tfeb<+>	C57BL/6N-Tfeb<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757800	M	MP:0001512	trunk curl	Tfeb<tm1b(EUCOMM)Wtsi>/Tfeb<+>	C57BL/6N-Tfeb<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757800	M	MP:0003961	decreased lean body mass	Tfeb<tm1b(EUCOMM)Wtsi>/Tfeb<+>	C57BL/6N-Tfeb<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757802	M	MP:0005292	improved glucose tolerance	Tgfb1i1<tm1b(KOMP)Wtsi>/Tgfb1i1<tm1b(KOMP)Wtsi>	C57BL/6N-Tgfb1i1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757802	M	MP:0005178	increased circulating cholesterol level	Tgfb1i1<tm1b(KOMP)Wtsi>/Tgfb1i1<tm1b(KOMP)Wtsi>	C57BL/6N-Tgfb1i1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757805	F	MP:0003019	increased circulating chloride level	Spmap2l<tm1b(KOMP)Wtsi>/Spmap2l<tm1b(KOMP)Wtsi>	C57BL/6N-Spmap2l<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757805	F	MP:0000745	tremors	Spmap2l<tm1b(KOMP)Wtsi>/Spmap2l<tm1b(KOMP)Wtsi>	C57BL/6N-Spmap2l<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5757806	M	MP:0002764	short tibia	Thra<tm1b(EUCOMM)Wtsi>/Thra<+>	C57BL/6N-Thra<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757806	F	MP:0001258	decreased body length	Thra<tm1b(EUCOMM)Wtsi>/Thra<+>	C57BL/6N-Thra<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757806	M	MP:0005292	improved glucose tolerance	Thra<tm1b(EUCOMM)Wtsi>/Thra<+>	C57BL/6N-Thra<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757808	F	MP:0001399	hyperactivity	Timm22<tm1b(KOMP)Wtsi>/Timm22<+>	C57BL/6N-Timm22<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757808	M	MP:0005633	increased circulating sodium level	Timm22<tm1b(KOMP)Wtsi>/Timm22<+>	C57BL/6N-Timm22<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757810	M	MP:0000062	increased bone mineral density	Timm50<tm1b(EUCOMM)Wtsi>/Timm50<+>	C57BL/6N-Timm50<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757810	M	MP:0010025	decreased total body fat amount	Timm50<tm1b(EUCOMM)Wtsi>/Timm50<+>	C57BL/6N-Timm50<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757810	M	MP:0002941	increased circulating alanine transaminase level	Timm50<tm1b(EUCOMM)Wtsi>/Timm50<+>	C57BL/6N-Timm50<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757810	M	MP:0010124	decreased bone mineral content	Timm50<tm1b(EUCOMM)Wtsi>/Timm50<+>	C57BL/6N-Timm50<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757810	M	MP:0001258	decreased body length	Timm50<tm1b(EUCOMM)Wtsi>/Timm50<+>	C57BL/6N-Timm50<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757810	M	MP:0003960	increased lean body mass	Timm50<tm1b(EUCOMM)Wtsi>/Timm50<+>	C57BL/6N-Timm50<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757812	M	MP:0000559	abnormal femur morphology	Timp1<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Timp1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757812	M	MP:0005296	abnormal humerus morphology	Timp1<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Timp1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757813	M	MP:0004931	enlarged epididymis	Tmem106b<tm2b(KOMP)Wtsi>/Tmem106b<tm2b(KOMP)Wtsi>	C57BL/6N-Tmem106b<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757813	M	MP:0002631	abnormal epididymis morphology	Tmem106b<tm2b(KOMP)Wtsi>/Tmem106b<tm2b(KOMP)Wtsi>	C57BL/6N-Tmem106b<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757813	M	MP:0002175	decreased brain weight	Tmem106b<tm2b(KOMP)Wtsi>/Tmem106b<tm2b(KOMP)Wtsi>	C57BL/6N-Tmem106b<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5757814	M	MP:0003961	decreased lean body mass	Tmem108<tm1b(EUCOMM)Wtsi>/Tmem108<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem108<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757814	M	MP:0010024	increased total body fat amount	Tmem108<tm1b(EUCOMM)Wtsi>/Tmem108<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem108<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757814	F	MP:0001312	abnormal cornea morphology	Tmem108<tm1b(EUCOMM)Wtsi>/Tmem108<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem108<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757814	M	MP:0010123	increased bone mineral content	Tmem108<tm1b(EUCOMM)Wtsi>/Tmem108<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem108<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757814	F	MP:0005343	increased circulating aspartate transaminase level	Tmem108<tm1b(EUCOMM)Wtsi>/Tmem108<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem108<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757815	F	MP:0002968	increased circulating alkaline phosphatase level	Stimate<tm2b(KOMP)Wtsi>/Stimate<tm2b(KOMP)Wtsi>	C57BL/6N-Stimate<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757816	M	MP:0010024	increased total body fat amount	Tmem132a<tm1b(KOMP)Wtsi>/Tmem132a<+>	C57BL/6N-Tmem132a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757817	M	MP:0001491	unresponsive to tactile stimuli	Tmem132a<tm1b(KOMP)Wtsi>/Tmem132a<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem132a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757817	F	MP:0005650	abnormal limb bud morphology	Tmem132a<tm1b(KOMP)Wtsi>/Tmem132a<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem132a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757817	F	MP:0003720	abnormal neural tube closure	Tmem132a<tm1b(KOMP)Wtsi>/Tmem132a<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem132a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757817	F	MP:0000428	abnormal craniofacial morphology	Tmem132a<tm1b(KOMP)Wtsi>/Tmem132a<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem132a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757817	M	MP:0001697	abnormal embryo size	Tmem132a<tm1b(KOMP)Wtsi>/Tmem132a<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem132a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757817	F	MP:0000438	abnormal cranium morphology	Tmem132a<tm1b(KOMP)Wtsi>/Tmem132a<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem132a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757817	M	MP:0011495	abnormal head shape	Tmem132a<tm1b(KOMP)Wtsi>/Tmem132a<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem132a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757817	M	MP:0003743	abnormal facial morphology	Tmem132a<tm1b(KOMP)Wtsi>/Tmem132a<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem132a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757818	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Tlcd5<tm1.1(KOMP)Vlcg>/Tlcd5<tm1.1(KOMP)Vlcg>	C57BL/6N-Tlcd5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757820	M	MP:0001513	limb grasping	Tmem63b<tm1b(EUCOMM)Wtsi>/Tmem63b<+>	C57BL/6N-Tmem63b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757820	F	MP:0001399	hyperactivity	Tmem63b<tm1b(EUCOMM)Wtsi>/Tmem63b<+>	C57BL/6N-Tmem63b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757820	F	MP:0002764	short tibia	Tmem63b<tm1b(EUCOMM)Wtsi>/Tmem63b<+>	C57BL/6N-Tmem63b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757822	M	MP:0001363	increased anxiety-related response	Tmod2<tm1b(KOMP)Wtsi>/Tmod2<tm1b(KOMP)Wtsi>	C57BL/6N-Tmod2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757822	M	MP:0002875	decreased erythrocyte cell number	Tmod2<tm1b(KOMP)Wtsi>/Tmod2<tm1b(KOMP)Wtsi>	C57BL/6N-Tmod2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757822	F	MP:0010124	decreased bone mineral content	Tmod2<tm1b(KOMP)Wtsi>/Tmod2<tm1b(KOMP)Wtsi>	C57BL/6N-Tmod2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757822	M	MP:0002874	decreased hemoglobin content	Tmod2<tm1b(KOMP)Wtsi>/Tmod2<tm1b(KOMP)Wtsi>	C57BL/6N-Tmod2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757822	F	MP:0000063	decreased bone mineral density	Tmod2<tm1b(KOMP)Wtsi>/Tmod2<tm1b(KOMP)Wtsi>	C57BL/6N-Tmod2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757822	F	MP:0003795	abnormal bone structure	Tmod2<tm1b(KOMP)Wtsi>/Tmod2<tm1b(KOMP)Wtsi>	C57BL/6N-Tmod2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5757824	M	MP:0002608	increased hematocrit	Tppp<tm1.1(KOMP)Vlcg>/Tppp<tm1.1(KOMP)Vlcg>	C57BL/6N-Tppp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757824	F	MP:0002968	increased circulating alkaline phosphatase level	Tppp<tm1.1(KOMP)Vlcg>/Tppp<tm1.1(KOMP)Vlcg>	C57BL/6N-Tppp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757824	F	MP:0004924	abnormal behavior	Tppp<tm1.1(KOMP)Vlcg>/Tppp<tm1.1(KOMP)Vlcg>	C57BL/6N-Tppp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757824	M	MP:0010052	increased grip strength	Tppp<tm1.1(KOMP)Vlcg>/Tppp<tm1.1(KOMP)Vlcg>	C57BL/6N-Tppp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757824	F	MP:0000947	convulsive seizures	Tppp<tm1.1(KOMP)Vlcg>/Tppp<tm1.1(KOMP)Vlcg>	C57BL/6N-Tppp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757824	M	MP:0008810	increased circulating iron level	Tppp<tm1.1(KOMP)Vlcg>/Tppp<tm1.1(KOMP)Vlcg>	C57BL/6N-Tppp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757824	F	MP:0001415	increased exploration in new environment	Tppp<tm1.1(KOMP)Vlcg>/Tppp<tm1.1(KOMP)Vlcg>	C57BL/6N-Tppp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757827	M	MP:0010025	decreased total body fat amount	Trim29<tm1b(EUCOMM)Wtsi>/Trim29<tm1b(EUCOMM)Wtsi>	C57BL/6N-Trim29<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757827	M	MP:0003960	increased lean body mass	Trim29<tm1b(EUCOMM)Wtsi>/Trim29<tm1b(EUCOMM)Wtsi>	C57BL/6N-Trim29<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757832	F	MP:0001513	limb grasping	Trpm1<tm1b(KOMP)Wtsi>/Trpm1<tm1b(KOMP)Wtsi>	C57BL/6N-Trpm1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757832	M	MP:0005293	impaired glucose tolerance	Trpm1<tm1b(KOMP)Wtsi>/Trpm1<tm1b(KOMP)Wtsi>	C57BL/6N-Trpm1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757832	F	MP:0010090	increased circulating creatine kinase level	Trpm1<tm1b(KOMP)Wtsi>/Trpm1<tm1b(KOMP)Wtsi>	C57BL/6N-Trpm1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757832	M	MP:0006243	impaired pupillary reflex	Trpm1<tm1b(KOMP)Wtsi>/Trpm1<tm1b(KOMP)Wtsi>	C57BL/6N-Trpm1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757832	M	MP:0002546	mydriasis	Trpm1<tm1b(KOMP)Wtsi>/Trpm1<tm1b(KOMP)Wtsi>	C57BL/6N-Trpm1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757833	M	MP:0009142	decreased prepulse inhibition	Tspyl2<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Tspyl2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757833	M	MP:0001399	hyperactivity	Tspyl2<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Tspyl2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757834	F	MP:0000218	increased leukocyte cell number	Ttc28<tm1b(EUCOMM)Hmgu>/Ttc28<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ttc28<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757834	F	MP:0000063	decreased bone mineral density	Ttc28<tm1b(EUCOMM)Hmgu>/Ttc28<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ttc28<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757834	M	MP:0009142	decreased prepulse inhibition	Ttc28<tm1b(EUCOMM)Hmgu>/Ttc28<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ttc28<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757834	M	MP:0000186	decreased circulating HDL cholesterol level	Ttc28<tm1b(EUCOMM)Hmgu>/Ttc28<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ttc28<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757834	M	MP:0005179	decreased circulating cholesterol level	Ttc28<tm1b(EUCOMM)Hmgu>/Ttc28<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ttc28<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757834	M	MP:0002968	increased circulating alkaline phosphatase level	Ttc28<tm1b(EUCOMM)Hmgu>/Ttc28<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ttc28<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757834	M	MP:0010067	increased red blood cell distribution width	Ttc28<tm1b(EUCOMM)Hmgu>/Ttc28<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ttc28<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757834	F	MP:0011110	preweaning lethality, incomplete penetrance	Ttc28<tm1b(EUCOMM)Hmgu>/Ttc28<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ttc28<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757834	F	MP:0005013	increased lymphocyte cell number	Ttc28<tm1b(EUCOMM)Hmgu>/Ttc28<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ttc28<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757835	M	MP:0005293	impaired glucose tolerance	Tulp3<tm1b(EUCOMM)Hmgu>/Tulp3<+>	C57BL/6N-Tulp3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757835	F	MP:0002941	increased circulating alanine transaminase level	Tulp3<tm1b(EUCOMM)Hmgu>/Tulp3<+>	C57BL/6N-Tulp3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757835	M	MP:0010024	increased total body fat amount	Tulp3<tm1b(EUCOMM)Hmgu>/Tulp3<+>	C57BL/6N-Tulp3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757835	F	MP:0005343	increased circulating aspartate transaminase level	Tulp3<tm1b(EUCOMM)Hmgu>/Tulp3<+>	C57BL/6N-Tulp3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757835	M	MP:0009142	decreased prepulse inhibition	Tulp3<tm1b(EUCOMM)Hmgu>/Tulp3<+>	C57BL/6N-Tulp3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757835	M	MP:0003961	decreased lean body mass	Tulp3<tm1b(EUCOMM)Hmgu>/Tulp3<+>	C57BL/6N-Tulp3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757835	F	MP:0013278	decreased fasting circulating glucose level	Tulp3<tm1b(EUCOMM)Hmgu>/Tulp3<+>	C57BL/6N-Tulp3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757837	F	MP:0010124	decreased bone mineral content	Txnip<tm1b(EUCOMM)Hmgu>/Txnip<tm1b(EUCOMM)Hmgu>	C57BL/6N-Txnip<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757837	F	MP:0001566	increased circulating phosphate level	Txnip<tm1b(EUCOMM)Hmgu>/Txnip<tm1b(EUCOMM)Hmgu>	C57BL/6N-Txnip<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757837	F	MP:0010024	increased total body fat amount	Txnip<tm1b(EUCOMM)Hmgu>/Txnip<tm1b(EUCOMM)Hmgu>	C57BL/6N-Txnip<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757838	M	MP:0001510	abnormal coat appearance	Ube2b<tm1b(EUCOMM)Wtsi>/Ube2b<+>	C57BL/6N-Ube2b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757838	M	MP:0002607	decreased basophil cell number	Ube2b<tm1b(EUCOMM)Wtsi>/Ube2b<+>	C57BL/6N-Ube2b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757838	M	MP:0001513	limb grasping	Ube2b<tm1b(EUCOMM)Wtsi>/Ube2b<+>	C57BL/6N-Ube2b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757838	M	MP:0000218	increased leukocyte cell number	Ube2b<tm1b(EUCOMM)Wtsi>/Ube2b<+>	C57BL/6N-Ube2b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757838	M	MP:0001406	abnormal gait	Ube2b<tm1b(EUCOMM)Wtsi>/Ube2b<+>	C57BL/6N-Ube2b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5757840	M	MP:0003961	decreased lean body mass	Ube2d3<tm1b(EUCOMM)Hmgu>/Ube2d3<+>	C57BL/6N-Ube2d3<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757840	M	MP:0010124	decreased bone mineral content	Ube2d3<tm1b(EUCOMM)Hmgu>/Ube2d3<+>	C57BL/6N-Ube2d3<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757840	M	MP:0000063	decreased bone mineral density	Ube2d3<tm1b(EUCOMM)Hmgu>/Ube2d3<+>	C57BL/6N-Ube2d3<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5757842	M	MP:0004738	abnormal auditory brainstem response	Ube2g1<tm1b(EUCOMM)Hmgu>/Ube2g1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ube2g1<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757842	M	MP:0000601	small liver	Ube2g1<tm1b(EUCOMM)Hmgu>/Ube2g1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ube2g1<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757842	M	MP:0001925	male infertility	Ube2g1<tm1b(EUCOMM)Hmgu>/Ube2g1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ube2g1<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757848	M	MP:0013279	increased fasting circulating glucose level	Ube2w<tm1b(EUCOMM)Wtsi>/Ube2w<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ube2w<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757849	F	MP:0001258	decreased body length	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757849	M	MP:0000218	increased leukocyte cell number	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757849	F	MP:0010024	increased total body fat amount	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757849	F	MP:0002968	increased circulating alkaline phosphatase level	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757849	M	MP:0011971	increased circulating lactate dehydrogenase level	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757849	M	MP:0001417	decreased exploration in new environment	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757849	M	MP:0005013	increased lymphocyte cell number	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757849	F	MP:0001406	abnormal gait	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757849	M	MP:0002834	decreased heart weight	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757849	F	MP:0002764	short tibia	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5757850	M	MP:0000219	increased neutrophil cell number	Ubox5<tm1b(EUCOMM)Hmgu>/Ubox5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ubox5<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757850	F	MP:0002092	abnormal eye morphology	Ubox5<tm1b(EUCOMM)Hmgu>/Ubox5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ubox5<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757852	M	MP:0002644	decreased circulating triglyceride level	Ucp1<tm1b(EUCOMM)Hmgu>/Ucp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ucp1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757852	F	MP:0004156	abnormal QT variability	Ucp1<tm1b(EUCOMM)Hmgu>/Ucp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ucp1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757852	M	MP:0001303	abnormal lens morphology	Ucp1<tm1b(EUCOMM)Hmgu>/Ucp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ucp1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757852	M	MP:0003131	increased erythrocyte cell number	Ucp1<tm1b(EUCOMM)Hmgu>/Ucp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ucp1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757852	F	MP:0002953	thick ventricular wall	Ucp1<tm1b(EUCOMM)Hmgu>/Ucp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ucp1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757852	M	MP:0002608	increased hematocrit	Ucp1<tm1b(EUCOMM)Hmgu>/Ucp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ucp1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757853	F	MP:0010024	increased total body fat amount	Uhrf2<tm1b(EUCOMM)Wtsi>/Uhrf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Uhrf2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757853	F	MP:0005333	decreased heart rate	Uhrf2<tm1b(EUCOMM)Wtsi>/Uhrf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Uhrf2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757853	F	MP:0003961	decreased lean body mass	Uhrf2<tm1b(EUCOMM)Wtsi>/Uhrf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Uhrf2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757853	F	MP:0001399	hyperactivity	Uhrf2<tm1b(EUCOMM)Wtsi>/Uhrf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Uhrf2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757853	F	MP:0003795	abnormal bone structure	Uhrf2<tm1b(EUCOMM)Wtsi>/Uhrf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Uhrf2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757853	F	MP:0005013	increased lymphocyte cell number	Uhrf2<tm1b(EUCOMM)Wtsi>/Uhrf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Uhrf2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757853	F	MP:0010506	prolonged RR interval	Uhrf2<tm1b(EUCOMM)Wtsi>/Uhrf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Uhrf2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757853	F	MP:0001258	decreased body length	Uhrf2<tm1b(EUCOMM)Wtsi>/Uhrf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Uhrf2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757853	F	MP:0000218	increased leukocyte cell number	Uhrf2<tm1b(EUCOMM)Wtsi>/Uhrf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Uhrf2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757853	F	MP:0002968	increased circulating alkaline phosphatase level	Uhrf2<tm1b(EUCOMM)Wtsi>/Uhrf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Uhrf2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757853	F	MP:0010124	decreased bone mineral content	Uhrf2<tm1b(EUCOMM)Wtsi>/Uhrf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Uhrf2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757853	F	MP:0001926	female infertility	Uhrf2<tm1b(EUCOMM)Wtsi>/Uhrf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Uhrf2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757853	F	MP:0000063	decreased bone mineral density	Uhrf2<tm1b(EUCOMM)Wtsi>/Uhrf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Uhrf2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5757854	F	MP:0001304	cataract	Uqcrb<tm1b(EUCOMM)Wtsi>/Uqcrb<+>	C57BL/6N-Uqcrb<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757854	M	MP:0000218	increased leukocyte cell number	Uqcrb<tm1b(EUCOMM)Wtsi>/Uqcrb<+>	C57BL/6N-Uqcrb<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757854	F	MP:0001303	abnormal lens morphology	Uqcrb<tm1b(EUCOMM)Wtsi>/Uqcrb<+>	C57BL/6N-Uqcrb<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757856	M	MP:0001406	abnormal gait	Atp5mk<tm1b(EUCOMM)Wtsi>/Atp5mk<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atp5mk<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757856	M	MP:0005419	decreased circulating serum albumin level	Atp5mk<tm1b(EUCOMM)Wtsi>/Atp5mk<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atp5mk<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757856	F	MP:0005565	increased blood urea nitrogen level	Atp5mk<tm1b(EUCOMM)Wtsi>/Atp5mk<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atp5mk<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757856	M	MP:0005343	increased circulating aspartate transaminase level	Atp5mk<tm1b(EUCOMM)Wtsi>/Atp5mk<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atp5mk<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757856	M	MP:0000219	increased neutrophil cell number	Atp5mk<tm1b(EUCOMM)Wtsi>/Atp5mk<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atp5mk<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757856	M	MP:0002941	increased circulating alanine transaminase level	Atp5mk<tm1b(EUCOMM)Wtsi>/Atp5mk<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atp5mk<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757856	M	MP:0001566	increased circulating phosphate level	Atp5mk<tm1b(EUCOMM)Wtsi>/Atp5mk<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atp5mk<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757856	M	MP:0000220	increased monocyte cell number	Atp5mk<tm1b(EUCOMM)Wtsi>/Atp5mk<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atp5mk<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757856	F	MP:0000218	increased leukocyte cell number	Atp5mk<tm1b(EUCOMM)Wtsi>/Atp5mk<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atp5mk<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757856	M	MP:0002874	decreased hemoglobin content	Atp5mk<tm1b(EUCOMM)Wtsi>/Atp5mk<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atp5mk<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757856	F	MP:0008806	increased circulating amylase level	Atp5mk<tm1b(EUCOMM)Wtsi>/Atp5mk<tm1b(EUCOMM)Wtsi>	C57BL/6N-Atp5mk<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757859	M	MP:0005293	impaired glucose tolerance	Usp12<tm1b(EUCOMM)Hmgu>/Usp12<tm1b(EUCOMM)Hmgu>	C57BL/6N-Usp12<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757859	F	MP:0002968	increased circulating alkaline phosphatase level	Usp12<tm1b(EUCOMM)Hmgu>/Usp12<tm1b(EUCOMM)Hmgu>	C57BL/6N-Usp12<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757859	F	MP:0005178	increased circulating cholesterol level	Usp12<tm1b(EUCOMM)Hmgu>/Usp12<tm1b(EUCOMM)Hmgu>	C57BL/6N-Usp12<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757862	F	MP:0000220	increased monocyte cell number	Usp22<tm1b(KOMP)Wtsi>/Usp22<+>	C57BL/6N-Usp22<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757862	M	MP:0001406	abnormal gait	Usp22<tm1b(KOMP)Wtsi>/Usp22<+>	C57BL/6N-Usp22<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757864	F	MP:0002591	decreased mean corpuscular volume	Usp2<tm1b(EUCOMM)Wtsi>/Usp2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Usp2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5757867	M	MP:0009142	decreased prepulse inhibition	Usp38<tm1b(EUCOMM)Hmgu>/Usp38<tm1b(EUCOMM)Hmgu>	C57BL/6N-Usp38<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757867	F	MP:0010506	prolonged RR interval	Usp38<tm1b(EUCOMM)Hmgu>/Usp38<tm1b(EUCOMM)Hmgu>	C57BL/6N-Usp38<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757867	F	MP:0005554	decreased circulating creatinine level	Usp38<tm1b(EUCOMM)Hmgu>/Usp38<tm1b(EUCOMM)Hmgu>	C57BL/6N-Usp38<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757867	M	MP:0001289	persistence of hyaloid vascular system	Usp38<tm1b(EUCOMM)Hmgu>/Usp38<tm1b(EUCOMM)Hmgu>	C57BL/6N-Usp38<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757867	F	MP:0002590	increased mean corpuscular volume	Usp38<tm1b(EUCOMM)Hmgu>/Usp38<tm1b(EUCOMM)Hmgu>	C57BL/6N-Usp38<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757867	M	MP:0003179	thrombocytopenia	Usp38<tm1b(EUCOMM)Hmgu>/Usp38<tm1b(EUCOMM)Hmgu>	C57BL/6N-Usp38<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757870	F	MP:0002968	increased circulating alkaline phosphatase level	Usp47<tm1b(EUCOMM)Wtsi>/Usp47<tm1b(EUCOMM)Wtsi>	C57BL/6N-Usp47<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757870	M	MP:0001556	increased circulating HDL cholesterol level	Usp47<tm1b(EUCOMM)Wtsi>/Usp47<tm1b(EUCOMM)Wtsi>	C57BL/6N-Usp47<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757870	M	MP:0005178	increased circulating cholesterol level	Usp47<tm1b(EUCOMM)Wtsi>/Usp47<tm1b(EUCOMM)Wtsi>	C57BL/6N-Usp47<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5757872	M	MP:0005567	decreased circulating total protein level	Usp54<tm1b(KOMP)Wtsi>/Usp54<tm1b(KOMP)Wtsi>	C57BL/6N-Usp54<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757872	M	MP:0005016	decreased lymphocyte cell number	Usp54<tm1b(KOMP)Wtsi>/Usp54<tm1b(KOMP)Wtsi>	C57BL/6N-Usp54<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757872	M	MP:0005343	increased circulating aspartate transaminase level	Usp54<tm1b(KOMP)Wtsi>/Usp54<tm1b(KOMP)Wtsi>	C57BL/6N-Usp54<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757872	M	MP:0002874	decreased hemoglobin content	Usp54<tm1b(KOMP)Wtsi>/Usp54<tm1b(KOMP)Wtsi>	C57BL/6N-Usp54<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757872	M	MP:0002941	increased circulating alanine transaminase level	Usp54<tm1b(KOMP)Wtsi>/Usp54<tm1b(KOMP)Wtsi>	C57BL/6N-Usp54<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757872	M	MP:0005419	decreased circulating serum albumin level	Usp54<tm1b(KOMP)Wtsi>/Usp54<tm1b(KOMP)Wtsi>	C57BL/6N-Usp54<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757872	M	MP:0010088	decreased circulating fructosamine level	Usp54<tm1b(KOMP)Wtsi>/Usp54<tm1b(KOMP)Wtsi>	C57BL/6N-Usp54<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757872	M	MP:0000219	increased neutrophil cell number	Usp54<tm1b(KOMP)Wtsi>/Usp54<tm1b(KOMP)Wtsi>	C57BL/6N-Usp54<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757872	M	MP:0000274	enlarged heart	Usp54<tm1b(KOMP)Wtsi>/Usp54<tm1b(KOMP)Wtsi>	C57BL/6N-Usp54<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757872	M	MP:0010067	increased red blood cell distribution width	Usp54<tm1b(KOMP)Wtsi>/Usp54<tm1b(KOMP)Wtsi>	C57BL/6N-Usp54<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757872	M	MP:0008805	decreased circulating amylase level	Usp54<tm1b(KOMP)Wtsi>/Usp54<tm1b(KOMP)Wtsi>	C57BL/6N-Usp54<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5757873	F	MP:0002959	increased urine microalbumin level	Vezt<tm1b(EUCOMM)Hmgu>/Vezt<+>	C57BL/6N-Vezt<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757873	M	MP:0002590	increased mean corpuscular volume	Vezt<tm1b(EUCOMM)Hmgu>/Vezt<+>	C57BL/6N-Vezt<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5757875	M	MP:0001925	male infertility	Vps13a<tm1b(EUCOMM)Wtsi>/Vps13a<tm1b(EUCOMM)Wtsi>	C57BL/6N-Vps13a<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757878	M	MP:0009142	decreased prepulse inhibition	Vps37d<tm2b(EUCOMM)Wtsi>/Vps37d<+>	C57BL/6N-Vps37d<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757878	F	MP:0003733	abnormal retina inner nuclear layer morphology	Vps37d<tm2b(EUCOMM)Wtsi>/Vps37d<+>	C57BL/6N-Vps37d<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5757880	M	MP:0000691	enlarged spleen	Vps4a<tm1b(EUCOMM)Hmgu>/Vps4a<+>	C57BL/6N-Vps4a<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5757880	M	MP:0004952	increased spleen weight	Vps4a<tm1b(EUCOMM)Hmgu>/Vps4a<+>	C57BL/6N-Vps4a<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5757880	M	MP:0002060	abnormal skin morphology	Vps4a<tm1b(EUCOMM)Hmgu>/Vps4a<+>	C57BL/6N-Vps4a<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5757882	M	MP:0005627	increased circulating potassium level	Vwa8<tm1b(EUCOMM)Wtsi>/Vwa8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Vwa8<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757882	M	MP:0013279	increased fasting circulating glucose level	Vwa8<tm1b(EUCOMM)Wtsi>/Vwa8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Vwa8<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757882	M	MP:0001325	abnormal retina morphology	Vwa8<tm1b(EUCOMM)Wtsi>/Vwa8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Vwa8<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5757883	M	MP:0005562	decreased mean corpuscular hemoglobin	Wars1<tm1b(EUCOMM)Hmgu>/Wars1<+>	C57BL/6N-Wars<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757883	M	MP:0000599	enlarged liver	Wars1<tm1b(EUCOMM)Hmgu>/Wars1<+>	C57BL/6N-Wars<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757883	M	MP:0011897	decreased circulating unsaturated transferrin level	Wars1<tm1b(EUCOMM)Hmgu>/Wars1<+>	C57BL/6N-Wars<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757883	M	MP:0000598	abnormal liver morphology	Wars1<tm1b(EUCOMM)Hmgu>/Wars1<+>	C57BL/6N-Wars<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757883	M	MP:0002968	increased circulating alkaline phosphatase level	Wars1<tm1b(EUCOMM)Hmgu>/Wars1<+>	C57BL/6N-Wars<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757883	F	MP:0001304	cataract	Wars1<tm1b(EUCOMM)Hmgu>/Wars1<+>	C57BL/6N-Wars<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757883	F	MP:0005140	decreased cardiac muscle contractility	Wars1<tm1b(EUCOMM)Hmgu>/Wars1<+>	C57BL/6N-Wars<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757883	M	MP:0001417	decreased exploration in new environment	Wars1<tm1b(EUCOMM)Hmgu>/Wars1<+>	C57BL/6N-Wars<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757883	M	MP:0002135	abnormal kidney morphology	Wars1<tm1b(EUCOMM)Hmgu>/Wars1<+>	C57BL/6N-Wars<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757883	M	MP:0002941	increased circulating alanine transaminase level	Wars1<tm1b(EUCOMM)Hmgu>/Wars1<+>	C57BL/6N-Wars<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757883	F	MP:0003131	increased erythrocyte cell number	Wars1<tm1b(EUCOMM)Hmgu>/Wars1<+>	C57BL/6N-Wars<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757883	F	MP:0005333	decreased heart rate	Wars1<tm1b(EUCOMM)Hmgu>/Wars1<+>	C57BL/6N-Wars<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757883	F	MP:0008528	polycystic kidney	Wars1<tm1b(EUCOMM)Hmgu>/Wars1<+>	C57BL/6N-Wars<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757887	F	MP:0001512	trunk curl	Nsd3<tm1b(EUCOMM)Hmgu>/Nsd3<+>	C57BL/6N-Nsd3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757888	M	MP:0000692	small spleen	Nsd3<tm1b(EUCOMM)Hmgu>/Nsd3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nsd3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757888	M	MP:0001488	increased startle reflex	Nsd3<tm1b(EUCOMM)Hmgu>/Nsd3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nsd3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757889	M	MP:0010123	increased bone mineral content	Wnt5b<tm1.1(KOMP)Vlcg>/Wnt5b<tm1.1(KOMP)Vlcg>	C57BL/6N-Wnt5b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757889	M	MP:0000062	increased bone mineral density	Wnt5b<tm1.1(KOMP)Vlcg>/Wnt5b<tm1.1(KOMP)Vlcg>	C57BL/6N-Wnt5b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5757891	F	MP:0005140	decreased cardiac muscle contractility	Wsb2<tm1b(EUCOMM)Hmgu>/Wsb2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Wsb2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757891	F	MP:0001402	decreased locomotor activity	Wsb2<tm1b(EUCOMM)Hmgu>/Wsb2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Wsb2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757891	F	MP:0002968	increased circulating alkaline phosphatase level	Wsb2<tm1b(EUCOMM)Hmgu>/Wsb2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Wsb2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757891	F	MP:0010097	abnormal retina blood vessel morphology	Wsb2<tm1b(EUCOMM)Hmgu>/Wsb2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Wsb2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757891	F	MP:0001926	female infertility	Wsb2<tm1b(EUCOMM)Hmgu>/Wsb2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Wsb2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757891	F	MP:0010052	increased grip strength	Wsb2<tm1b(EUCOMM)Hmgu>/Wsb2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Wsb2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757891	F	MP:0001399	hyperactivity	Wsb2<tm1b(EUCOMM)Hmgu>/Wsb2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Wsb2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757891	M	MP:0001925	male infertility	Wsb2<tm1b(EUCOMM)Hmgu>/Wsb2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Wsb2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5757894	M	MP:0003743	abnormal facial morphology	Xpot<tm3b(EUCOMM)Hmgu>/Xpot<tm3b(EUCOMM)Hmgu>	C57BL/6N-Xpot<tm3b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5757894	M	MP:0001697	abnormal embryo size	Xpot<tm3b(EUCOMM)Hmgu>/Xpot<tm3b(EUCOMM)Hmgu>	C57BL/6N-Xpot<tm3b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5757894	M	MP:0011100	preweaning lethality, complete penetrance	Xpot<tm3b(EUCOMM)Hmgu>/Xpot<tm3b(EUCOMM)Hmgu>	C57BL/6N-Xpot<tm3b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5757897	F	MP:0000063	decreased bone mineral density	Ydjc<tm1.1(KOMP)Vlcg>/Ydjc<tm1.1(KOMP)Vlcg>	C57BL/6N-Ydjc<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757897	F	MP:0005560	decreased circulating glucose level	Ydjc<tm1.1(KOMP)Vlcg>/Ydjc<tm1.1(KOMP)Vlcg>	C57BL/6N-Ydjc<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757897	M	MP:0005633	increased circulating sodium level	Ydjc<tm1.1(KOMP)Vlcg>/Ydjc<tm1.1(KOMP)Vlcg>	C57BL/6N-Ydjc<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757897	M	MP:0005564	increased hemoglobin content	Ydjc<tm1.1(KOMP)Vlcg>/Ydjc<tm1.1(KOMP)Vlcg>	C57BL/6N-Ydjc<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757897	F	MP:0002968	increased circulating alkaline phosphatase level	Ydjc<tm1.1(KOMP)Vlcg>/Ydjc<tm1.1(KOMP)Vlcg>	C57BL/6N-Ydjc<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757898	M	MP:0011965	decreased total retina thickness	Yipf5<tm1b(EUCOMM)Hmgu>/Yipf5<+>	C57BL/6N-Yipf5<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757898	F	MP:0009141	increased prepulse inhibition	Yipf5<tm1b(EUCOMM)Hmgu>/Yipf5<+>	C57BL/6N-Yipf5<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757898	M	MP:0002953	thick ventricular wall	Yipf5<tm1b(EUCOMM)Hmgu>/Yipf5<+>	C57BL/6N-Yipf5<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757898	M	MP:0002875	decreased erythrocyte cell number	Yipf5<tm1b(EUCOMM)Hmgu>/Yipf5<+>	C57BL/6N-Yipf5<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5757900	M	MP:0000702	enlarged lymph nodes	Ywhaz<tm1b(EUCOMM)Hmgu>/Ywhaz<+>	C57BL/6N-Ywhaz<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757900	M	MP:0000218	increased leukocyte cell number	Ywhaz<tm1b(EUCOMM)Hmgu>/Ywhaz<+>	C57BL/6N-Ywhaz<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757900	F	MP:0002060	abnormal skin morphology	Ywhaz<tm1b(EUCOMM)Hmgu>/Ywhaz<+>	C57BL/6N-Ywhaz<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757900	M	MP:0005013	increased lymphocyte cell number	Ywhaz<tm1b(EUCOMM)Hmgu>/Ywhaz<+>	C57BL/6N-Ywhaz<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757900	M	MP:0002764	short tibia	Ywhaz<tm1b(EUCOMM)Hmgu>/Ywhaz<+>	C57BL/6N-Ywhaz<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757901	M	MP:0001488	increased startle reflex	Zbtb24<tm1b(EUCOMM)Hmgu>/Zbtb24<+>	C57BL/6N-Zbtb24<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757901	M	MP:0010097	abnormal retina blood vessel morphology	Zbtb24<tm1b(EUCOMM)Hmgu>/Zbtb24<+>	C57BL/6N-Zbtb24<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757901	M	MP:0002792	abnormal retina vasculature morphology	Zbtb24<tm1b(EUCOMM)Hmgu>/Zbtb24<+>	C57BL/6N-Zbtb24<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757901	F	MP:0001303	abnormal lens morphology	Zbtb24<tm1b(EUCOMM)Hmgu>/Zbtb24<+>	C57BL/6N-Zbtb24<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757904	M	MP:0013279	increased fasting circulating glucose level	Zdhhc2<tm1b(KOMP)Wtsi>/Zdhhc2<tm1b(KOMP)Wtsi>	C57BL/6N-Zdhhc2<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757904	M	MP:0003769	abnormal lip morphology	Zdhhc2<tm1b(KOMP)Wtsi>/Zdhhc2<tm1b(KOMP)Wtsi>	C57BL/6N-Zdhhc2<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757904	M	MP:0002753	dilated heart left ventricle	Zdhhc2<tm1b(KOMP)Wtsi>/Zdhhc2<tm1b(KOMP)Wtsi>	C57BL/6N-Zdhhc2<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5757905	M	MP:0000218	increased leukocyte cell number	Zfp119a<tm1b(EUCOMM)Hmgu>/Zfp119a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp119a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5757906	M	MP:0005016	decreased lymphocyte cell number	Zfp207<tm1b(EUCOMM)Hmgu>/Zfp207<+>	C57BL/6N-Zfp207<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757906	M	MP:0005419	decreased circulating serum albumin level	Zfp207<tm1b(EUCOMM)Hmgu>/Zfp207<+>	C57BL/6N-Zfp207<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757906	M	MP:0000219	increased neutrophil cell number	Zfp207<tm1b(EUCOMM)Hmgu>/Zfp207<+>	C57BL/6N-Zfp207<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757906	F	MP:0002591	decreased mean corpuscular volume	Zfp207<tm1b(EUCOMM)Hmgu>/Zfp207<+>	C57BL/6N-Zfp207<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757906	F	MP:0005554	decreased circulating creatinine level	Zfp207<tm1b(EUCOMM)Hmgu>/Zfp207<+>	C57BL/6N-Zfp207<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5757908	F	MP:0001406	abnormal gait	Zfp287<tm1b(EUCOMM)Wtsi>/Zfp287<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp287<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757909	F	MP:0000218	increased leukocyte cell number	Zfp36<tm1(KOMP)Vlcg>/Zfp36<+>	C57BL/6N-Zfp36<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757909	M	MP:0013279	increased fasting circulating glucose level	Zfp36<tm1(KOMP)Vlcg>/Zfp36<+>	C57BL/6N-Zfp36<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5757911	M	MP:0002060	abnormal skin morphology	Zfp451<tm1b(EUCOMM)Hmgu>/Zfp451<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp451<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757911	M	MP:0001944	abnormal pancreas morphology	Zfp451<tm1b(EUCOMM)Hmgu>/Zfp451<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp451<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757911	M	MP:0001417	decreased exploration in new environment	Zfp451<tm1b(EUCOMM)Hmgu>/Zfp451<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp451<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5757913	F	MP:0013279	increased fasting circulating glucose level	Zfp616<tm1b(KOMP)Wtsi>/Zfp616<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp616<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5757914	F	MP:0000208	decreased hematocrit	Zfp689<tm1.1(KOMP)Vlcg>/Zfp689<tm1.1(KOMP)Vlcg>	C57BL/6N-Zfp689<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757914	M	MP:0001523	impaired righting response	Zfp689<tm1.1(KOMP)Vlcg>/Zfp689<tm1.1(KOMP)Vlcg>	C57BL/6N-Zfp689<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757914	F	MP:0011396	abnormal sleep behavior	Zfp689<tm1.1(KOMP)Vlcg>/Zfp689<tm1.1(KOMP)Vlcg>	C57BL/6N-Zfp689<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757914	M	MP:0005505	thrombocytosis	Zfp689<tm1.1(KOMP)Vlcg>/Zfp689<tm1.1(KOMP)Vlcg>	C57BL/6N-Zfp689<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5757916	F	MP:0008810	increased circulating iron level	Zfyve28<tm1b(EUCOMM)Wtsi>/Zfyve28<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfyve28<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5759069	M	MP:0005012	decreased eosinophil cell number	Acvr2a<tm1.1(KOMP)Vlcg>/Acvr2a<+>	C57BL/6N-Acvr2a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5759069	M	MP:0000222	decreased neutrophil cell number	Acvr2a<tm1.1(KOMP)Vlcg>/Acvr2a<+>	C57BL/6N-Acvr2a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5759069	F	MP:0002797	increased thigmotaxis	Acvr2a<tm1.1(KOMP)Vlcg>/Acvr2a<+>	C57BL/6N-Acvr2a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5759069	F	MP:0004924	abnormal behavior	Acvr2a<tm1.1(KOMP)Vlcg>/Acvr2a<+>	C57BL/6N-Acvr2a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5759105	F	MP:0020870	decreased thigmotaxis	Asf1a<tm1b(KOMP)Wtsi>/Asf1a<+>	B6N(Cg)-Asf1a<tm1b(KOMP)Wtsi>/2J	N	MGI:5576271
MGI:5759105	M	MP:0002968	increased circulating alkaline phosphatase level	Asf1a<tm1b(KOMP)Wtsi>/Asf1a<+>	B6N(Cg)-Asf1a<tm1b(KOMP)Wtsi>/2J	N	MGI:5576271
MGI:5759129	M	MP:0001289	persistence of hyaloid vascular system	Casz1<tm1b(EUCOMM)Hmgu>/Casz1<+>	C57BL/6N-Casz1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5759135	M	MP:0009552	urinary bladder obstruction	Ccnb1<tm1b(KOMP)Wtsi>/Ccnb1<+>	C57BL/6N-Ccnb1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5759135	F	MP:0000745	tremors	Ccnb1<tm1b(KOMP)Wtsi>/Ccnb1<+>	C57BL/6N-Ccnb1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5759148	M	MP:0005343	increased circulating aspartate transaminase level	Chrnb2<tm1b(EUCOMM)Hmgu>/Chrnb2<+>	C57BL/6N-Chrnb2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5759148	F	MP:0001289	persistence of hyaloid vascular system	Chrnb2<tm1b(EUCOMM)Hmgu>/Chrnb2<+>	C57BL/6N-Chrnb2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5759152	M	MP:0000221	decreased leukocyte cell number	Clcf1<tm1.1(KOMP)Vlcg>/Clcf1<+>	C57BL/6N-Clcf1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5759152	M	MP:0003233	prolonged QT interval	Clcf1<tm1.1(KOMP)Vlcg>/Clcf1<+>	C57BL/6N-Clcf1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5759152	M	MP:0000062	increased bone mineral density	Clcf1<tm1.1(KOMP)Vlcg>/Clcf1<+>	C57BL/6N-Clcf1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5759152	M	MP:0010123	increased bone mineral content	Clcf1<tm1.1(KOMP)Vlcg>/Clcf1<+>	C57BL/6N-Clcf1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5759178	F	MP:0002968	increased circulating alkaline phosphatase level	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5759182	M	MP:0010123	increased bone mineral content	Ddx41<tm1b(KOMP)Wtsi>/Ddx41<+>	C57BL/6N-Ddx41<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5759189	F	MP:0010087	increased circulating fructosamine level	Dnajc17<tm1b(EUCOMM)Hmgu>/Dnajc17<+>	C57BL/6N-Dnajc17<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5759213	M	MP:0002079	increased circulating insulin level	Exosc8<tm1.1(KOMP)Vlcg>/Exosc8<+>	C57BL/6N-Exosc8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759213	M	MP:0005561	increased mean corpuscular hemoglobin	Exosc8<tm1.1(KOMP)Vlcg>/Exosc8<+>	C57BL/6N-Exosc8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759235	M	MP:0002135	abnormal kidney morphology	Flii<tm1b(KOMP)Mbp>/Flii<+>	C57BL/6N-Flii<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5759257	F	MP:0005564	increased hemoglobin content	Gpnmb<tm1.1(KOMP)Vlcg>/Gpnmb<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpnmb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5759266	M	MP:0002753	dilated heart left ventricle	Hells<tm1b(EUCOMM)Wtsi>/Hells<+>	C57BL/6N-Hells<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5759266	M	MP:0011951	increased cardiac stroke volume	Hells<tm1b(EUCOMM)Wtsi>/Hells<+>	C57BL/6N-Hells<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5759283	F	MP:0012362	increased large unstained cell number	Ikzf5<tm1(KOMP)Wtsi>/Ikzf5<tm1(KOMP)Wtsi>	C57BL/6N-Ikzf5<tm1(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5759283	F	MP:0003795	abnormal bone structure	Ikzf5<tm1(KOMP)Wtsi>/Ikzf5<tm1(KOMP)Wtsi>	C57BL/6N-Ikzf5<tm1(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5759283	F	MP:0000063	decreased bone mineral density	Ikzf5<tm1(KOMP)Wtsi>/Ikzf5<tm1(KOMP)Wtsi>	C57BL/6N-Ikzf5<tm1(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5759283	M	MP:0004738	abnormal auditory brainstem response	Ikzf5<tm1(KOMP)Wtsi>/Ikzf5<tm1(KOMP)Wtsi>	C57BL/6N-Ikzf5<tm1(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5759283	F	MP:0010124	decreased bone mineral content	Ikzf5<tm1(KOMP)Wtsi>/Ikzf5<tm1(KOMP)Wtsi>	C57BL/6N-Ikzf5<tm1(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5759292	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Il6st<tm1b(KOMP)Mbp>/Il6st<+>	C57BL/6N-Il6st<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5759292	M	MP:0005344	increased circulating bilirubin level	Il6st<tm1b(KOMP)Mbp>/Il6st<+>	C57BL/6N-Il6st<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5759293	M	MP:0001697	abnormal embryo size	Ilk<tm1.1(KOMP)Vlcg>/Ilk<+>	C57BL/6N-Ilk<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759293	M	MP:0002574	increased vertical activity	Ilk<tm1.1(KOMP)Vlcg>/Ilk<+>	C57BL/6N-Ilk<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759293	F	MP:0001566	increased circulating phosphate level	Ilk<tm1.1(KOMP)Vlcg>/Ilk<+>	C57BL/6N-Ilk<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759295	M	MP:0006203	eye hemorrhage	Inpp5e<tm1.1(KOMP)Vlcg>/Inpp5e<+>	C57BL/6N-Inpp5e<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5759296	F	MP:0004151	decreased circulating iron level	Ipo11<tm1.1(KOMP)Vlcg>/Ipo11<+>	C57BL/6N-Ipo11<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759309	F	MP:0013279	increased fasting circulating glucose level	Kntc1<tm1b(EUCOMM)Hmgu>/Kntc1<+>	C57BL/6N-Kntc1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5759340	M	MP:0020870	decreased thigmotaxis	Msx1<tm1b(KOMP)Wtsi>/Msx1<+>	C57BL/6N-Msx1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5759340	M	MP:0002833	increased heart weight	Msx1<tm1b(KOMP)Wtsi>/Msx1<+>	C57BL/6N-Msx1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5759340	M	MP:0001554	increased circulating free fatty acids level	Msx1<tm1b(KOMP)Wtsi>/Msx1<+>	C57BL/6N-Msx1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5759341	M	MP:0000137	abnormal vertebrae morphology	Mtch2<tm1b(EUCOMM)Hmgu>/Mtch2<+>	C57BL/6N-Mtch2<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5759367	F	MP:0005559	increased circulating glucose level	Oas1g<tm1b(KOMP)Wtsi>/Oas1g<+>	C57BL/6N-Oas1g<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5759413	M	MP:0001488	increased startle reflex	Psen1<tm1.1(KOMP)Vlcg>/Psen1<+>	C57BL/6N-Psen1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759414	F	MP:0011436	decreased urine magnesium level	Ptms<tm1.1(KOMP)Wtsi>/Ptms<+>	C57BL/6N-Ptms<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5759414	M	MP:0001566	increased circulating phosphate level	Ptms<tm1.1(KOMP)Wtsi>/Ptms<+>	C57BL/6N-Ptms<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5759414	F	MP:0001417	decreased exploration in new environment	Ptms<tm1.1(KOMP)Wtsi>/Ptms<+>	C57BL/6N-Ptms<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5759419	M	MP:0013279	increased fasting circulating glucose level	Rab34<tm1b(EUCOMM)Hmgu>/Rab34<+>	C57BL/6N-Rab34<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5759426	F	MP:0005561	increased mean corpuscular hemoglobin	Rdx<tm1.1(KOMP)Vlcg>/Rdx<+>	C57BL/6N-Rdx<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759428	M	MP:0000195	decreased circulating calcium level	Rgp1<tm1.1(KOMP)Vlcg>/Rgp1<+>	C57BL/6N-Rgp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759428	M	MP:0005560	decreased circulating glucose level	Rgp1<tm1.1(KOMP)Vlcg>/Rgp1<+>	C57BL/6N-Rgp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759428	F	MP:0020870	decreased thigmotaxis	Rgp1<tm1.1(KOMP)Vlcg>/Rgp1<+>	C57BL/6N-Rgp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759428	F	MP:0000955	abnormal spinal cord morphology	Rgp1<tm1.1(KOMP)Vlcg>/Rgp1<+>	C57BL/6N-Rgp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759428	F	MP:0004924	abnormal behavior	Rgp1<tm1.1(KOMP)Vlcg>/Rgp1<+>	C57BL/6N-Rgp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759439	F	MP:0003795	abnormal bone structure	Mrm3<tm1.1(KOMP)Vlcg>/Mrm3<+>	C57BL/6N-Mrm3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759439	M	MP:0009142	decreased prepulse inhibition	Mrm3<tm1.1(KOMP)Vlcg>/Mrm3<+>	C57BL/6N-Mrm3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759440	M	MP:0002968	increased circulating alkaline phosphatase level	Rora<tm1b(EUCOMM)Wtsi>/Rora<+>	C57BL/6N-Rora<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5759444	M	MP:0002574	increased vertical activity	S100a6<tm1b(KOMP)Wtsi>/S100a6<+>	C57BL/6N-S100a6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5759444	M	MP:0010378	increased respiratory quotient	S100a6<tm1b(KOMP)Wtsi>/S100a6<+>	C57BL/6N-S100a6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5759456	M	MP:0013279	increased fasting circulating glucose level	Siva1<tm1b(EUCOMM)Hmgu>/Siva1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Siva1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5759462	M	MP:0005627	increased circulating potassium level	Slc46a1<tm1b(KOMP)Mbp>/Slc46a1<+>	C57BL/6N-Slc46a1<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5759462	M	MP:0005344	increased circulating bilirubin level	Slc46a1<tm1b(KOMP)Mbp>/Slc46a1<+>	C57BL/6N-Slc46a1<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5759462	M	MP:0005343	increased circulating aspartate transaminase level	Slc46a1<tm1b(KOMP)Mbp>/Slc46a1<+>	C57BL/6N-Slc46a1<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5759462	M	MP:0004151	decreased circulating iron level	Slc46a1<tm1b(KOMP)Mbp>/Slc46a1<+>	C57BL/6N-Slc46a1<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5759466	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Slc6a5<tm1.1(KOMP)Vlcg>/Slc6a5<+>	C57BL/6N-Slc6a5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5759470	M	MP:0005633	increased circulating sodium level	Snapin<tm1.1(KOMP)Vlcg>/Snapin<+>	C57BL/6N-Snapin<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759470	M	MP:0005627	increased circulating potassium level	Snapin<tm1.1(KOMP)Vlcg>/Snapin<+>	C57BL/6N-Snapin<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759470	M	MP:0002941	increased circulating alanine transaminase level	Snapin<tm1.1(KOMP)Vlcg>/Snapin<+>	C57BL/6N-Snapin<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759484	F	MP:0005560	decreased circulating glucose level	Stx18<tm2b(KOMP)Wtsi>/Stx18<+>	C57BL/6N-Stx18<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5759522	M	MP:0001147	small testis	Unc13b<tm1b(KOMP)Wtsi>/Unc13b<+>	C57BL/6N-Unc13b<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5759522	M	MP:0001146	abnormal testis morphology	Unc13b<tm1b(KOMP)Wtsi>/Unc13b<+>	C57BL/6N-Unc13b<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5759527	M	MP:0005560	decreased circulating glucose level	Vax1<tm1b(KOMP)Mbp>/Vax1<+>	C57BL/6N-Vax1<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5759527	F	MP:0004122	abnormal sinus arrhythmia	Vax1<tm1b(KOMP)Mbp>/Vax1<+>	C57BL/6N-Vax1<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5759531	M	MP:0003961	decreased lean body mass	Vps25<tm1.1(KOMP)Vlcg>/Vps25<+>	C57BL/6N-Vps25<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5759531	M	MP:0002834	decreased heart weight	Vps25<tm1.1(KOMP)Vlcg>/Vps25<+>	C57BL/6N-Vps25<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5759531	M	MP:0010024	increased total body fat amount	Vps25<tm1.1(KOMP)Vlcg>/Vps25<+>	C57BL/6N-Vps25<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5759533	M	MP:0000955	abnormal spinal cord morphology	Wars2<tm1.1(KOMP)Vlcg>/Wars2<+>	C57BL/6N-Wars2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759540	F	MP:0002591	decreased mean corpuscular volume	Xrcc3<tm1b(KOMP)Mbp>/Xrcc3<+>	C57BL/6N-Xrcc3<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5759551	F	MP:0005561	increased mean corpuscular hemoglobin	Zwilch<tm1.1(KOMP)Vlcg>/Zwilch<+>	C57BL/6N-Zwilch<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5759551	M	MP:0004151	decreased circulating iron level	Zwilch<tm1.1(KOMP)Vlcg>/Zwilch<+>	C57BL/6N-Zwilch<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5760005	F	MP:0006352	decreased glycosylated hemoglobin level	Gria1<tm1Lex>/Gria1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	MGI:2655403
MGI:5760039	M	MP:0002727	decreased circulating insulin level	Glo1<Gt(VICTR48)1493Lex>/Glo1<Gt(VICTR48)1493Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	MGI:2655403
MGI:5760055	F	MP:0008028	pregnancy-related premature death	Ddr2<tm1.1(cre/Esr1*)Rcow>/Ddr2<tm1.1(cre/Esr1*)Rcow>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	24993042
MGI:5760303	M	MP:0001155	arrest of spermatogenesis	yahsmts3/yahsmts3	C3HeB/FeJ-yahsmts3	N	MGI:2655403
MGI:5760303	M	MP:0001925	male infertility	yahsmts3/yahsmts3	C3HeB/FeJ-yahsmts3	N	MGI:2655403
MGI:5760303	M	MP:0001147	small testis	yahsmts3/yahsmts3	C3HeB/FeJ-yahsmts3	N	MGI:2655403
MGI:5760316	M	MP:0001155	arrest of spermatogenesis	yahsmts2/yahsmts2	C3HeB/FeJ-yahsmts2	N	MGI:2655403
MGI:5760316	M	MP:0001147	small testis	yahsmts2/yahsmts2	C3HeB/FeJ-yahsmts2	N	MGI:2655403
MGI:5760316	M	MP:0001925	male infertility	yahsmts2/yahsmts2	C3HeB/FeJ-yahsmts2	N	MGI:2655403
MGI:5760327	M	MP:0001147	small testis	yahsmts/yahsmts	C3HeB/FeJ-yahsmts	N	MGI:2655403
MGI:5760327	M	MP:0001155	arrest of spermatogenesis	yahsmts/yahsmts	C3HeB/FeJ-yahsmts	N	MGI:2655403
MGI:5760327	M	MP:0001925	male infertility	yahsmts/yahsmts	C3HeB/FeJ-yahsmts	N	MGI:2655403
MGI:5760334	M	MP:0001155	arrest of spermatogenesis	yahsmts6/yahsmts6	C3HeB/FeJ-yahsmts6	N	MGI:2655403
MGI:5760334	M	MP:0001925	male infertility	yahsmts6/yahsmts6	C3HeB/FeJ-yahsmts6	N	MGI:2655403
MGI:5760334	M	MP:0001147	small testis	yahsmts6/yahsmts6	C3HeB/FeJ-yahsmts6	N	MGI:2655403
MGI:5760339	M	MP:0001147	small testis	yahsmts5/yahsmts5	C3HeB/FeJ-yahsmts5	N	MGI:2655403
MGI:5760339	M	MP:0001925	male infertility	yahsmts5/yahsmts5	C3HeB/FeJ-yahsmts5	N	MGI:2655403
MGI:5760339	M	MP:0001155	arrest of spermatogenesis	yahsmts5/yahsmts5	C3HeB/FeJ-yahsmts5	N	MGI:2655403
MGI:5760349	M	MP:0001155	arrest of spermatogenesis	yahsmts4/yahsmts4	C3HeB/FeJ-yahsmts4	N	MGI:2655403
MGI:5760349	M	MP:0001925	male infertility	yahsmts4/yahsmts4	C3HeB/FeJ-yahsmts4	N	MGI:2655403
MGI:5760349	M	MP:0001147	small testis	yahsmts4/yahsmts4	C3HeB/FeJ-yahsmts4	N	MGI:2655403
MGI:5760386	M	MP:0003917	increased kidney weight	Pramel17<tm1b(KOMP)Wtsi>/Pramel17<tm1b(KOMP)Wtsi>	C57BL/6N-Pramel17<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5760386	M	MP:0002111	abnormal tail morphology	Pramel17<tm1b(KOMP)Wtsi>/Pramel17<tm1b(KOMP)Wtsi>	C57BL/6N-Pramel17<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5760386	M	MP:0000274	enlarged heart	Pramel17<tm1b(KOMP)Wtsi>/Pramel17<tm1b(KOMP)Wtsi>	C57BL/6N-Pramel17<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5760387	M	MP:0000702	enlarged lymph nodes	Nat8f2<tm1.1(KOMP)Vlcg>/Nat8f2<tm1.1(KOMP)Vlcg>	C57BL/6N-Nat8f2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5762713	M	MP:0031355	abnormal proacrosomal vesicle fusion	Smap2<tm1Sata>/Smap2<tm1Sata>	involves: 129P2/OlaHsd * C57BL/6J	N	23864717
MGI:5762713	M	MP:0009647	decreased fertilization frequency	Smap2<tm1Sata>/Smap2<tm1Sata>	involves: 129P2/OlaHsd * C57BL/6J	N	23864717
MGI:5762713	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Smap2<tm1Sata>/Smap2<tm1Sata>	involves: 129P2/OlaHsd * C57BL/6J	N	23864717
MGI:5762713	M	MP:0009231	detached acrosome	Smap2<tm1Sata>/Smap2<tm1Sata>	involves: 129P2/OlaHsd * C57BL/6J	N	23864717
MGI:5762713	M	MP:0008898	abnormal acrosome morphology	Smap2<tm1Sata>/Smap2<tm1Sata>	involves: 129P2/OlaHsd * C57BL/6J	N	23864717
MGI:5762713	M	MP:0001925	male infertility	Smap2<tm1Sata>/Smap2<tm1Sata>	involves: 129P2/OlaHsd * C57BL/6J	N	23864717
MGI:5762713	M	MP:0031389	abnormal ectoplasmic specialization morphology	Smap2<tm1Sata>/Smap2<tm1Sata>	involves: 129P2/OlaHsd * C57BL/6J	N	23864717
MGI:5762713	F	MP:0005389	reproductive system phenotype	Smap2<tm1Sata>/Smap2<tm1Sata>	involves: 129P2/OlaHsd * C57BL/6J	Y	23864717
MGI:5762713	M	MP:0002686	globozoospermia	Smap2<tm1Sata>/Smap2<tm1Sata>	involves: 129P2/OlaHsd * C57BL/6J	N	23864717
MGI:5762713	M	MP:0009377	ectopic manchette	Smap2<tm1Sata>/Smap2<tm1Sata>	involves: 129P2/OlaHsd * C57BL/6J	N	23864717
MGI:5762713	M	MP:0002675	asthenozoospermia	Smap2<tm1Sata>/Smap2<tm1Sata>	involves: 129P2/OlaHsd * C57BL/6J	N	23864717
MGI:5762713	M	MP:0031354	abnormal acrosome assembly	Smap2<tm1Sata>/Smap2<tm1Sata>	involves: 129P2/OlaHsd * C57BL/6J	N	23864717
MGI:5762713	M	MP:0001932	abnormal spermiogenesis	Smap2<tm1Sata>/Smap2<tm1Sata>	involves: 129P2/OlaHsd * C57BL/6J	N	23864717
MGI:5762842	F	MP:0004856	decreased ovary weight	Nsmf<tm1a(KOMP)Wtsi>/Nsmf<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	25731822
MGI:5762842	F	MP:0008335	decreased gonadotroph cell number	Nsmf<tm1a(KOMP)Wtsi>/Nsmf<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	25731822
MGI:5762842	M	MP:0001922	reduced male fertility	Nsmf<tm1a(KOMP)Wtsi>/Nsmf<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	25731822
MGI:5762842	F	MP:0001923	reduced female fertility	Nsmf<tm1a(KOMP)Wtsi>/Nsmf<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	25731822
MGI:5762842	F	MP:0004905	decreased uterus weight	Nsmf<tm1a(KOMP)Wtsi>/Nsmf<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	25731822
MGI:5762842	F	MP:0001938	delayed sexual maturation	Nsmf<tm1a(KOMP)Wtsi>/Nsmf<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	25731822
MGI:5762842	F	MP:0002636	delayed vaginal opening	Nsmf<tm1a(KOMP)Wtsi>/Nsmf<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	25731822
MGI:5762843	F	MP:0001935	decreased litter size	Nsmf<tm1a(KOMP)Wtsi>/Nsmf<+>	involves: C57BL/6N	N	25731822
MGI:5762843	M	MP:0005389	reproductive system phenotype	Nsmf<tm1a(KOMP)Wtsi>/Nsmf<+>	involves: C57BL/6N	Y	25731822
MGI:5762843	F	MP:0001923	reduced female fertility	Nsmf<tm1a(KOMP)Wtsi>/Nsmf<+>	involves: C57BL/6N	N	25731822
MGI:5762922	M	MP:0003109	short femur	Epyc<tm1Mhok>/Epyc<tm1Mhok>	involves: 129S7/SvEvBrd * C57BL/6J	N	19932218
MGI:5762988	F	MP:0002041	increased pituitary adenoma incidence	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0001885	mammary gland duct hyperplasia	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0000630	mammary gland hyperplasia	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0001272	increased metastatic potential	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0006271	abnormal involution of the mammary gland	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0002035	increased leiomyosarcoma incidence	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0009506	abnormal mammary gland alveolus morphology	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0002027	increased lung adenocarcinoma incidence	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0010172	abnormal mammary gland epithelium physiology	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0010299	increased mammary gland tumor incidence	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0004702	increased circulating insulin-like growth factor I level	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0009503	abnormal mammary gland duct morphology	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5762988	F	MP:0009504	abnormal mammary gland epithelium morphology	Tg(MMTV-NCOA3)#Mybr/0	FVB/N-Tg(MMTV-NCOA3)#Mybr	N	15380517
MGI:5763024	F	MP:0010279	increased gastrointestinal tumor incidence	Rag2<tm1Fwa>/Rag2<tm1Fwa>,Stat1<tm1Rds>/Stat1<tm1Rds>	involves: 129S/SvEv * 129S6/SvEvTac	N	22264274
MGI:5763024	F	MP:0001883	increased mammary adenocarcinoma incidence	Rag2<tm1Fwa>/Rag2<tm1Fwa>,Stat1<tm1Rds>/Stat1<tm1Rds>	involves: 129S/SvEv * 129S6/SvEvTac	N	22264274
MGI:5763059	M	MP:0004910	decreased seminal vesicle weight	Mfsd14a<tm1Coll>/Mfsd14a<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	27107036
MGI:5763059	M	MP:0008839	absent acrosome	Mfsd14a<tm1Coll>/Mfsd14a<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	27107036
MGI:5763059	F	MP:0005389	reproductive system phenotype	Mfsd14a<tm1Coll>/Mfsd14a<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	Y	27107036
MGI:5763059	M	MP:0001932	abnormal spermiogenesis	Mfsd14a<tm1Coll>/Mfsd14a<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	27107036
MGI:5763059	M	MP:0002687	oligozoospermia	Mfsd14a<tm1Coll>/Mfsd14a<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	27107036
MGI:5763059	M	MP:0001925	male infertility	Mfsd14a<tm1Coll>/Mfsd14a<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	27107036
MGI:5763059	M	MP:0001262	decreased body weight	Mfsd14a<tm1Coll>/Mfsd14a<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	27107036
MGI:5763059	M	MP:0009833	absent sperm mitochondrial sheath	Mfsd14a<tm1Coll>/Mfsd14a<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	27107036
MGI:5763059	M	MP:0009230	abnormal sperm head morphology	Mfsd14a<tm1Coll>/Mfsd14a<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	27107036
MGI:5763059	M	MP:0002686	globozoospermia	Mfsd14a<tm1Coll>/Mfsd14a<tm1Coll>	involves: 129S/SvEv * 129S6/SvEvTac	N	27107036
MGI:5763076	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTV-ENPP2)20Gbm/0	FVB/N-Tg(MMTV-ENPP2)20Gbm	N	19477432
MGI:5763076	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-ENPP2)20Gbm/0	FVB/N-Tg(MMTV-ENPP2)20Gbm	N	19477432
MGI:5763076	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-ENPP2)20Gbm/0	FVB/N-Tg(MMTV-ENPP2)20Gbm	N	19477432
MGI:5763078	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-ENPP2)21Gbm/0	FVB/N-Tg(MMTV-ENPP2)21Gbm	N	19477432
MGI:5763078	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-ENPP2)21Gbm/0	FVB/N-Tg(MMTV-ENPP2)21Gbm	N	19477432
MGI:5763080	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-ENPP2)#Gbm/0	FVB/N-Tg(MMTV-ENPP2)#Gbm	N	19477432
MGI:5763080	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-ENPP2)#Gbm/0	FVB/N-Tg(MMTV-ENPP2)#Gbm	N	19477432
MGI:5763080	F	MP:0013148	mastitis	Tg(MMTV-ENPP2)#Gbm/0	FVB/N-Tg(MMTV-ENPP2)#Gbm	N	19477432
MGI:5763087	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-LPAR1)27Gbm/Tg(MMTV-LPAR1)27Gbm	FVB/N-Tg(MMTV-LPAR1)27Gbm	N	19477432
MGI:5763087	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-LPAR1)27Gbm/Tg(MMTV-LPAR1)27Gbm	FVB/N-Tg(MMTV-LPAR1)27Gbm	N	19477432
MGI:5763090	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-LPAR1)2Gbm/Tg(MMTV-LPAR1)2Gbm	FVB/N-Tg(MMTV-LPAR1)2Gbm	N	19477432
MGI:5763090	F	MP:0013148	mastitis	Tg(MMTV-LPAR1)2Gbm/Tg(MMTV-LPAR1)2Gbm	FVB/N-Tg(MMTV-LPAR1)2Gbm	N	19477432
MGI:5763090	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-LPAR1)2Gbm/Tg(MMTV-LPAR1)2Gbm	FVB/N-Tg(MMTV-LPAR1)2Gbm	N	19477432
MGI:5763094	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-LPAR1)7Gbm/Tg(MMTV-LPAR1)7Gbm	FVB/N-Tg(MMTV-LPAR1)7Gbm	N	19477432
MGI:5763094	F	MP:0013148	mastitis	Tg(MMTV-LPAR1)7Gbm/Tg(MMTV-LPAR1)7Gbm	FVB/N-Tg(MMTV-LPAR1)7Gbm	N	19477432
MGI:5763094	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-LPAR1)7Gbm/Tg(MMTV-LPAR1)7Gbm	FVB/N-Tg(MMTV-LPAR1)7Gbm	N	19477432
MGI:5763094	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTV-LPAR1)7Gbm/Tg(MMTV-LPAR1)7Gbm	FVB/N-Tg(MMTV-LPAR1)7Gbm	N	19477432
MGI:5763097	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-LPAR1)#Gbm/Tg(MMTV-LPAR1)#Gbm	FVB/N-Tg(MMTV-LPAR1)#Gbm	N	19477432
MGI:5763097	F	MP:0001272	increased metastatic potential	Tg(MMTV-LPAR1)#Gbm/Tg(MMTV-LPAR1)#Gbm	FVB/N-Tg(MMTV-LPAR1)#Gbm	N	19477432
MGI:5763097	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-LPAR1)#Gbm/Tg(MMTV-LPAR1)#Gbm	FVB/N-Tg(MMTV-LPAR1)#Gbm	N	19477432
MGI:5763097	F	MP:0013148	mastitis	Tg(MMTV-LPAR1)#Gbm/Tg(MMTV-LPAR1)#Gbm	FVB/N-Tg(MMTV-LPAR1)#Gbm	N	19477432
MGI:5763101	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-LPAR2)3Gbm/Tg(MMTV-LPAR2)3Gbm	FVB/N-Tg(MMTV-LPAR2)3Gbm	N	19477432
MGI:5763101	F	MP:0013148	mastitis	Tg(MMTV-LPAR2)3Gbm/Tg(MMTV-LPAR2)3Gbm	FVB/N-Tg(MMTV-LPAR2)3Gbm	N	19477432
MGI:5763101	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-LPAR2)3Gbm/Tg(MMTV-LPAR2)3Gbm	FVB/N-Tg(MMTV-LPAR2)3Gbm	N	19477432
MGI:5763104	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-LPAR2)6Gbm/Tg(MMTV-LPAR2)6Gbm	FVB/N-Tg(MMTV-LPAR2)6Gbm	N	19477432
MGI:5763104	F	MP:0013148	mastitis	Tg(MMTV-LPAR2)6Gbm/Tg(MMTV-LPAR2)6Gbm	FVB/N-Tg(MMTV-LPAR2)6Gbm	N	19477432
MGI:5763104	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-LPAR2)6Gbm/Tg(MMTV-LPAR2)6Gbm	FVB/N-Tg(MMTV-LPAR2)6Gbm	N	19477432
MGI:5763104	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTV-LPAR2)6Gbm/Tg(MMTV-LPAR2)6Gbm	FVB/N-Tg(MMTV-LPAR2)6Gbm	N	19477432
MGI:5763106	F	MP:0001272	increased metastatic potential	Tg(MMTV-LPAR2)#Gbm/Tg(MMTV-LPAR2)#Gbm	FVB/N-Tg(MMTV-LPAR2)#Gbm	N	19477432
MGI:5763106	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-LPAR2)#Gbm/Tg(MMTV-LPAR2)#Gbm	FVB/N-Tg(MMTV-LPAR2)#Gbm	N	19477432
MGI:5763106	F	MP:0013148	mastitis	Tg(MMTV-LPAR2)#Gbm/Tg(MMTV-LPAR2)#Gbm	FVB/N-Tg(MMTV-LPAR2)#Gbm	N	19477432
MGI:5763106	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-LPAR2)#Gbm/Tg(MMTV-LPAR2)#Gbm	FVB/N-Tg(MMTV-LPAR2)#Gbm	N	19477432
MGI:5763109	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-LPAR3)22Gbm/Tg(MMTV-LPAR3)22Gbm	FVB/N-Tg(MMTV-LPAR3)22Gbm	N	19477432
MGI:5763109	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-LPAR3)22Gbm/Tg(MMTV-LPAR3)22Gbm	FVB/N-Tg(MMTV-LPAR3)22Gbm	N	19477432
MGI:5763111	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTV-LPAR3)3Gbm/Tg(MMTV-LPAR3)3Gbm	FVB/N-Tg(MMTV-LPAR3)3Gbm	N	19477432
MGI:5763111	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-LPAR3)3Gbm/Tg(MMTV-LPAR3)3Gbm	FVB/N-Tg(MMTV-LPAR3)3Gbm	N	19477432
MGI:5763111	F	MP:0013148	mastitis	Tg(MMTV-LPAR3)3Gbm/Tg(MMTV-LPAR3)3Gbm	FVB/N-Tg(MMTV-LPAR3)3Gbm	N	19477432
MGI:5763111	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-LPAR3)3Gbm/Tg(MMTV-LPAR3)3Gbm	FVB/N-Tg(MMTV-LPAR3)3Gbm	N	19477432
MGI:5763113	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-LPAR3)#Gbm/Tg(MMTV-LPAR3)#Gbm	FVB/N-Tg(MMTV-LPAR3)#Gbm	N	19477432
MGI:5763113	F	MP:0001272	increased metastatic potential	Tg(MMTV-LPAR3)#Gbm/Tg(MMTV-LPAR3)#Gbm	FVB/N-Tg(MMTV-LPAR3)#Gbm	N	19477432
MGI:5763113	F	MP:0013148	mastitis	Tg(MMTV-LPAR3)#Gbm/Tg(MMTV-LPAR3)#Gbm	FVB/N-Tg(MMTV-LPAR3)#Gbm	N	19477432
MGI:5763113	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(MMTV-LPAR3)#Gbm/Tg(MMTV-LPAR3)#Gbm	FVB/N-Tg(MMTV-LPAR3)#Gbm	N	19477432
MGI:5763143	M	MP:0009237	kinked sperm flagellum	Ap1g1<fgt>/Ap1g1<fgt>	C57BL/6-Ap1g1<fgt>/KjnBoc	N	27090238
MGI:5763143	M	MP:0001922	reduced male fertility	Ap1g1<fgt>/Ap1g1<fgt>	C57BL/6-Ap1g1<fgt>/KjnBoc	N	27090238
MGI:5763143	M	MP:0004901	decreased male germ cell number	Ap1g1<fgt>/Ap1g1<fgt>	C57BL/6-Ap1g1<fgt>/KjnBoc	N	27090238
MGI:5763143	M	MP:0002687	oligozoospermia	Ap1g1<fgt>/Ap1g1<fgt>	C57BL/6-Ap1g1<fgt>/KjnBoc	N	27090238
MGI:5763180	F	MP:0001360	abnormal social investigation	L1cam<tm1(tTA)Msch>/L1cam<+>	129.Cg-L1cam<tm1(tTA)Msch>	N	26079769
MGI:5763180	F	MP:0001441	increased grooming behavior	L1cam<tm1(tTA)Msch>/L1cam<+>	129.Cg-L1cam<tm1(tTA)Msch>	N	26079769
MGI:5763180	F	MP:0005386	behavior/neurological phenotype	L1cam<tm1(tTA)Msch>/L1cam<+>	129.Cg-L1cam<tm1(tTA)Msch>	Y	26079769
MGI:5763180	F	MP:0011275	abnormal behavioral response to light	L1cam<tm1(tTA)Msch>/L1cam<+>	129.Cg-L1cam<tm1(tTA)Msch>	N	26079769
MGI:5763181	M	MP:0005289	increased oxygen consumption	Adamts7<tm1a(KOMP)Wtsi>/Adamts7<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	25712208
MGI:5763181	F	MP:0001405	impaired coordination	Adamts7<tm1a(KOMP)Wtsi>/Adamts7<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	25712208
MGI:5763241	F	MP:0004892	increased adiponectin level	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	28432106
MGI:5763241	F	MP:0005182	increased circulating estradiol level	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	28432106
MGI:5763241	M	MP:0005293	impaired glucose tolerance	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	24947361
MGI:5763241	M	MP:0002970	abnormal white adipose tissue morphology	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	24947361
MGI:5763241	F	MP:0001261	obese	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	28432106
MGI:5763241	M	MP:0000005	increased brown adipose tissue amount	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	24947361
MGI:5763241	F	MP:0002680	decreased corpora lutea number	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	28432106
MGI:5763241	F	MP:0001926	female infertility	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	28432106
MGI:5763241	M	MP:0005669	increased circulating leptin level	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	24947361
MGI:5763241	F	MP:0008869	anovulation	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	28432106
MGI:5763241	F	MP:0002644	decreased circulating triglyceride level	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	24947361
MGI:5763241	M	MP:0005670	abnormal white adipose tissue physiology	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	24947361
MGI:5763241	M	MP:0005331	insulin resistance	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	24947361
MGI:5763241	F	MP:0002016	ovary cyst	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	28432106
MGI:5763241	F	MP:0004832	enlarged ovary	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	28432106
MGI:5763241	F	MP:0005452	abnormal adipose tissue amount	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	28432106
MGI:5763241	F	MP:0003442	decreased circulating glycerol level	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	24947361
MGI:5763241	F	MP:0001129	impaired ovarian folliculogenesis	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	28432106
MGI:5763241	F	MP:0001923	reduced female fertility	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	28432106
MGI:5763241	F	MP:0005179	decreased circulating cholesterol level	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	24947361
MGI:5763241	M	MP:0001554	increased circulating free fatty acids level	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	24947361
MGI:5763241	M	MP:0002079	increased circulating insulin level	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	24947361
MGI:5763241	M	MP:0011613	decreased circulating ghrelin level	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	24947361
MGI:5763241	F	MP:0004892	increased adiponectin level	Tg(Fabp4-Phb)#Smis/0	involves: CD-1	N	24947361
MGI:5763275	M	MP:0004901	decreased male germ cell number	Tg(RNU6-RNAi:Rhox3)2Wilk/0,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	25790000
MGI:5763275	M	MP:0001153	small seminiferous tubules	Tg(RNU6-RNAi:Rhox3)2Wilk/0,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	25790000
MGI:5763275	M	MP:0014052	increased male germ cell apoptosis	Tg(RNU6-RNAi:Rhox3)2Wilk/0,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	25790000
MGI:5763275	M	MP:0001925	male infertility	Tg(RNU6-RNAi:Rhox3)2Wilk/0,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	25790000
MGI:5763275	M	MP:0002687	oligozoospermia	Tg(RNU6-RNAi:Rhox3)2Wilk/0,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	25790000
MGI:5763275	M	MP:0006380	abnormal spermatid morphology	Tg(RNU6-RNAi:Rhox3)2Wilk/0,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	25790000
MGI:5763275	M	MP:0005169	abnormal male meiosis	Tg(RNU6-RNAi:Rhox3)2Wilk/0,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	25790000
MGI:5763275	M	MP:0004852	decreased testis weight	Tg(RNU6-RNAi:Rhox3)2Wilk/0,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	25790000
MGI:5763276	M	MP:0005389	reproductive system phenotype	Rhox<tm1.1Wilk>/Rhox<tm1.1Wilk>	Not Specified	Y	25790000
MGI:5763276	M	MP:0001147	small testis	Rhox<tm1.1Wilk>/Rhox<tm1.1Wilk>	Not Specified	N	25790000
MGI:5763276	M	MP:0001153	small seminiferous tubules	Rhox<tm1.1Wilk>/Rhox<tm1.1Wilk>	Not Specified	N	25790000
MGI:5763276	M	MP:0004901	decreased male germ cell number	Rhox<tm1.1Wilk>/Rhox<tm1.1Wilk>	Not Specified	N	25790000
MGI:5763277	M	MP:0004901	decreased male germ cell number	Rhox<tm1Wilk>/Rhox<tm1Wilk>,Tg(RNU6-RNAi:Rhox3)2Wilk/0,Tg(Stra8-icre)1Reb/0	involves: 129 * FVB/NJ	N	25790000
MGI:5763277	M	MP:0002687	oligozoospermia	Rhox<tm1Wilk>/Rhox<tm1Wilk>,Tg(RNU6-RNAi:Rhox3)2Wilk/0,Tg(Stra8-icre)1Reb/0	involves: 129 * FVB/NJ	N	25790000
MGI:5763277	M	MP:0004852	decreased testis weight	Rhox<tm1Wilk>/Rhox<tm1Wilk>,Tg(RNU6-RNAi:Rhox3)2Wilk/0,Tg(Stra8-icre)1Reb/0	involves: 129 * FVB/NJ	N	25790000
MGI:5763277	M	MP:0002216	abnormal seminiferous tubule morphology	Rhox<tm1Wilk>/Rhox<tm1Wilk>,Tg(RNU6-RNAi:Rhox3)2Wilk/0,Tg(Stra8-icre)1Reb/0	involves: 129 * FVB/NJ	N	25790000
MGI:5763310	M	MP:0000702	enlarged lymph nodes	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763310	M	MP:0000689	abnormal spleen morphology	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763310	M	MP:0005293	impaired glucose tolerance	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763310	M	MP:0002339	abnormal lymph node morphology	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763310	M	MP:0005013	increased lymphocyte cell number	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763310	M	MP:0000691	enlarged spleen	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763310	F	MP:0011612	increased circulating ghrelin level	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763310	F	MP:0002078	abnormal glucose homeostasis	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763310	M	MP:0002079	increased circulating insulin level	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763310	M	MP:0005669	increased circulating leptin level	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763310	M	MP:0004702	increased circulating insulin-like growth factor I level	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763310	M	MP:0011613	decreased circulating ghrelin level	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763310	F	MP:0004892	increased adiponectin level	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763310	M	MP:0010209	abnormal circulating chemokine level	Tg(Fabp4-Phb*Y114F)#Smis/0	Not Specified	N	26751773
MGI:5763438	M	MP:0003789	increased osteosarcoma incidence	Smarca4<tm1Mag>/Smarca4<+>	involves: 129S/Sv * C57BL/6J * CD-1	N	17637742
MGI:5763443	M	MP:0003667	increased hemangiosarcoma incidence	Smarca2<tm1Mya>/Smarca2<tm1Mya>,Smarca4<tm1Mag>/Smarca4<+>	involves: 129S/Sv * 129S2/SvPas * C57BL/6J * CD-1	N	17637742
MGI:5763443	F	MP:0010299	increased mammary gland tumor incidence	Smarca2<tm1Mya>/Smarca2<tm1Mya>,Smarca4<tm1Mag>/Smarca4<+>	involves: 129S/Sv * 129S2/SvPas * C57BL/6J * CD-1	N	17637742
MGI:5763612	M	MP:0003313	abnormal locomotor activation	Itpr3<tf>/Itpr3<tf>	BTBR T<+> Itpr3<tf>/J	N	17559418
MGI:5763612	M	MP:0001364	decreased anxiety-related response	Itpr3<tf>/Itpr3<tf>	BTBR T<+> Itpr3<tf>/J	N	17559418
MGI:5763612	M	MP:0001441	increased grooming behavior	Itpr3<tf>/Itpr3<tf>	BTBR T<+> Itpr3<tf>/J	N	17559418
MGI:5763612	M	MP:0001360	abnormal social investigation	Itpr3<tf>/Itpr3<tf>	BTBR T<+> Itpr3<tf>/J	N	17559418
MGI:5763612	M	MP:0011000	abnormal allogrooming behavior	Itpr3<tf>/Itpr3<tf>	BTBR T<+> Itpr3<tf>/J	N	17559418
MGI:5763612	M	MP:0002969	impaired social transmission of food preference	Itpr3<tf>/Itpr3<tf>	BTBR T<+> Itpr3<tf>/J	N	17559418
MGI:5763824	F	MP:0002590	increased mean corpuscular volume	Acsf2<tm1.1(KOMP)Vlcg>/Acsf2<tm1.1(KOMP)Vlcg>	B6N(Cg)-Acsf2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763824	F	MP:0001399	hyperactivity	Acsf2<tm1.1(KOMP)Vlcg>/Acsf2<tm1.1(KOMP)Vlcg>	B6N(Cg)-Acsf2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763825	M	MP:0005560	decreased circulating glucose level	Adar<tm1b(EUCOMM)Wtsi>/Adar<+>	B6N(Cg)-Adar<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5763827	M	MP:0013279	increased fasting circulating glucose level	Adora2b<tm1.1(KOMP)Vlcg>/Adora2b<+>	B6N(Cg)-Adora2b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763828	F	MP:0002968	increased circulating alkaline phosphatase level	Adora2b<tm1.1(KOMP)Vlcg>/Adora2b<tm1.1(KOMP)Vlcg>	B6N(Cg)-Adora2b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763828	M	MP:0005560	decreased circulating glucose level	Adora2b<tm1.1(KOMP)Vlcg>/Adora2b<tm1.1(KOMP)Vlcg>	B6N(Cg)-Adora2b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763830	F	MP:0005564	increased hemoglobin content	Ahrr<tm1b(KOMP)Wtsi>/Ahrr<tm1b(KOMP)Wtsi>	B6N(Cg)-Ahrr<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763831	M	MP:0005343	increased circulating aspartate transaminase level	Ajap1<tm1b(EUCOMM)Hmgu>/Ajap1<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Ajap1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5763831	M	MP:0002941	increased circulating alanine transaminase level	Ajap1<tm1b(EUCOMM)Hmgu>/Ajap1<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Ajap1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5763831	F	MP:0010124	decreased bone mineral content	Ajap1<tm1b(EUCOMM)Hmgu>/Ajap1<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Ajap1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5763831	M	MP:0005627	increased circulating potassium level	Ajap1<tm1b(EUCOMM)Hmgu>/Ajap1<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Ajap1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5763831	F	MP:0003795	abnormal bone structure	Ajap1<tm1b(EUCOMM)Hmgu>/Ajap1<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Ajap1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5763831	F	MP:0005633	increased circulating sodium level	Ajap1<tm1b(EUCOMM)Hmgu>/Ajap1<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Ajap1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5763831	F	MP:0003019	increased circulating chloride level	Ajap1<tm1b(EUCOMM)Hmgu>/Ajap1<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Ajap1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5763831	F	MP:0005568	increased circulating total protein level	Ajap1<tm1b(EUCOMM)Hmgu>/Ajap1<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Ajap1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5763832	F	MP:0010052	increased grip strength	Arrb2<tm1.1(KOMP)Vlcg>/Arrb2<tm1.1(KOMP)Vlcg>	B6N(Cg)-Arrb2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763832	F	MP:0001566	increased circulating phosphate level	Arrb2<tm1.1(KOMP)Vlcg>/Arrb2<tm1.1(KOMP)Vlcg>	B6N(Cg)-Arrb2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763832	F	MP:0002968	increased circulating alkaline phosphatase level	Arrb2<tm1.1(KOMP)Vlcg>/Arrb2<tm1.1(KOMP)Vlcg>	B6N(Cg)-Arrb2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763833	M	MP:0002941	increased circulating alanine transaminase level	Arrdc1<tm1.1(KOMP)Vlcg>/Arrdc1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Arrdc1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763834	F	MP:0005633	increased circulating sodium level	Atrip<tm1b(KOMP)Wtsi>/Atrip<+>	B6N(Cg)-Atrip<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763834	F	MP:0003019	increased circulating chloride level	Atrip<tm1b(KOMP)Wtsi>/Atrip<+>	B6N(Cg)-Atrip<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763836	M	MP:0000062	increased bone mineral density	Bach1<tm1.1(KOMP)Vlcg>/Bach1<+>	B6N(Cg)-Bach1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763836	F	MP:0013279	increased fasting circulating glucose level	Bach1<tm1.1(KOMP)Vlcg>/Bach1<+>	B6N(Cg)-Bach1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763836	F	MP:0005385	cardiovascular system phenotype	Bach1<tm1.1(KOMP)Vlcg>/Bach1<+>	B6N(Cg)-Bach1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763836	M	MP:0010123	increased bone mineral content	Bach1<tm1.1(KOMP)Vlcg>/Bach1<+>	B6N(Cg)-Bach1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763836	M	MP:0002833	increased heart weight	Bach1<tm1.1(KOMP)Vlcg>/Bach1<+>	B6N(Cg)-Bach1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763836	F	MP:0003928	increased heart rate variability	Bach1<tm1.1(KOMP)Vlcg>/Bach1<+>	B6N(Cg)-Bach1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763838	M	MP:0020870	decreased thigmotaxis	Bbs4<tm1b(EUCOMM)Hmgu>/Bbs4<+>	B6N(Cg)-Bbs4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5763838	M	MP:0001417	decreased exploration in new environment	Bbs4<tm1b(EUCOMM)Hmgu>/Bbs4<+>	B6N(Cg)-Bbs4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5763840	F	MP:0001303	abnormal lens morphology	Bbs7<tm1b(EUCOMM)Wtsi>/Bbs7<+>	B6N(Cg)-Bbs7<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5763840	M	MP:0002941	increased circulating alanine transaminase level	Bbs7<tm1b(EUCOMM)Wtsi>/Bbs7<+>	B6N(Cg)-Bbs7<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5763840	M	MP:0005633	increased circulating sodium level	Bbs7<tm1b(EUCOMM)Wtsi>/Bbs7<+>	B6N(Cg)-Bbs7<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5763842	M	MP:0001575	cyanosis	Bclaf1<tm1b(EUCOMM)Wtsi>/Bclaf1<tm1b(EUCOMM)Wtsi>	B6N(Cg)-Bclaf1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5763843	M	MP:0003019	increased circulating chloride level	C1qa<tm1b(EUCOMM)Wtsi>/C1qa<tm1b(EUCOMM)Wtsi>	B6N(Cg)-C1qa<tm1b(EUCOMM)Wtsi>/3J	N	MGI:5576271
MGI:5763843	M	MP:0005560	decreased circulating glucose level	C1qa<tm1b(EUCOMM)Wtsi>/C1qa<tm1b(EUCOMM)Wtsi>	B6N(Cg)-C1qa<tm1b(EUCOMM)Wtsi>/3J	N	MGI:5576271
MGI:5763844	M	MP:0001402	decreased locomotor activity	Cyb5d2<tm1.1(KOMP)Wtsi>/Cyb5d2<tm1.1(KOMP)Wtsi>	B6N(Cg)-Cyb5d2<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763844	M	MP:0002833	increased heart weight	Cyb5d2<tm1.1(KOMP)Wtsi>/Cyb5d2<tm1.1(KOMP)Wtsi>	B6N(Cg)-Cyb5d2<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763844	M	MP:0020870	decreased thigmotaxis	Cyb5d2<tm1.1(KOMP)Wtsi>/Cyb5d2<tm1.1(KOMP)Wtsi>	B6N(Cg)-Cyb5d2<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763844	F	MP:0001488	increased startle reflex	Cyb5d2<tm1.1(KOMP)Wtsi>/Cyb5d2<tm1.1(KOMP)Wtsi>	B6N(Cg)-Cyb5d2<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763846	M	MP:0011435	increased urine magnesium level	Mrpl51<tm1.1(KOMP)Vlcg>/Mrpl51<+>	B6N(Cg)-Mrpl51<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763849	M	MP:0002833	increased heart weight	Polr2h<tm1.1(KOMP)Wtsi>/Polr2h<+>	B6N(Cg)-Polr2h<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763849	F	MP:0004151	decreased circulating iron level	Polr2h<tm1.1(KOMP)Wtsi>/Polr2h<+>	B6N(Cg)-Polr2h<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763849	F	MP:0005634	decreased circulating sodium level	Polr2h<tm1.1(KOMP)Wtsi>/Polr2h<+>	B6N(Cg)-Polr2h<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763851	M	MP:0002833	increased heart weight	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	B6N(Cg)-Prkab1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763851	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	B6N(Cg)-Prkab1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763851	M	MP:0000208	decreased hematocrit	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	B6N(Cg)-Prkab1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763851	M	MP:0002874	decreased hemoglobin content	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	B6N(Cg)-Prkab1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763851	F	MP:0005344	increased circulating bilirubin level	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	B6N(Cg)-Prkab1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763851	M	MP:0002875	decreased erythrocyte cell number	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	B6N(Cg)-Prkab1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763851	M	MP:0002591	decreased mean corpuscular volume	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	B6N(Cg)-Prkab1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5763853	M	MP:0001556	increased circulating HDL cholesterol level	Rfc1<tm1b(KOMP)Mbp>/Rfc1<+>	B6N(Cg)-Rfc1<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5763853	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Rfc1<tm1b(KOMP)Mbp>/Rfc1<+>	B6N(Cg)-Rfc1<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5763856	M	MP:0010052	increased grip strength	Ube2o<tm1.1(KOMP)Mbp>/Ube2o<+>	B6N(Cg)-Ube2o<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5763856	M	MP:0002941	increased circulating alanine transaminase level	Ube2o<tm1.1(KOMP)Mbp>/Ube2o<+>	B6N(Cg)-Ube2o<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5763856	M	MP:0005178	increased circulating cholesterol level	Ube2o<tm1.1(KOMP)Mbp>/Ube2o<+>	B6N(Cg)-Ube2o<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5763858	F	MP:0001399	hyperactivity	Zbtb4<tm1.1(KOMP)Vlcg>/Zbtb4<tm1.1(KOMP)Vlcg>	B6N(Cg)-Zbtb4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763858	M	MP:0001307	fused cornea and lens	Zbtb4<tm1.1(KOMP)Vlcg>/Zbtb4<tm1.1(KOMP)Vlcg>	B6N(Cg)-Zbtb4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763858	M	MP:0005633	increased circulating sodium level	Zbtb4<tm1.1(KOMP)Vlcg>/Zbtb4<tm1.1(KOMP)Vlcg>	B6N(Cg)-Zbtb4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763858	F	MP:0011396	abnormal sleep behavior	Zbtb4<tm1.1(KOMP)Vlcg>/Zbtb4<tm1.1(KOMP)Vlcg>	B6N(Cg)-Zbtb4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763858	F	MP:0003019	increased circulating chloride level	Zbtb4<tm1.1(KOMP)Vlcg>/Zbtb4<tm1.1(KOMP)Vlcg>	B6N(Cg)-Zbtb4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763858	M	MP:0001289	persistence of hyaloid vascular system	Zbtb4<tm1.1(KOMP)Vlcg>/Zbtb4<tm1.1(KOMP)Vlcg>	B6N(Cg)-Zbtb4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763859	M	MP:0005179	decreased circulating cholesterol level	Zzef1<tm2.1(KOMP)Vlcg>/Zzef1<tm2.1(KOMP)Vlcg>	B6N(Cg)-Zzef1<tm2.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763859	F	MP:0002075	abnormal coat/hair pigmentation	Zzef1<tm2.1(KOMP)Vlcg>/Zzef1<tm2.1(KOMP)Vlcg>	B6N(Cg)-Zzef1<tm2.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763859	M	MP:0001399	hyperactivity	Zzef1<tm2.1(KOMP)Vlcg>/Zzef1<tm2.1(KOMP)Vlcg>	B6N(Cg)-Zzef1<tm2.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763859	M	MP:0005627	increased circulating potassium level	Zzef1<tm2.1(KOMP)Vlcg>/Zzef1<tm2.1(KOMP)Vlcg>	B6N(Cg)-Zzef1<tm2.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763859	F	MP:0002968	increased circulating alkaline phosphatase level	Zzef1<tm2.1(KOMP)Vlcg>/Zzef1<tm2.1(KOMP)Vlcg>	B6N(Cg)-Zzef1<tm2.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763859	M	MP:0000186	decreased circulating HDL cholesterol level	Zzef1<tm2.1(KOMP)Vlcg>/Zzef1<tm2.1(KOMP)Vlcg>	B6N(Cg)-Zzef1<tm2.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763859	M	MP:0005343	increased circulating aspartate transaminase level	Zzef1<tm2.1(KOMP)Vlcg>/Zzef1<tm2.1(KOMP)Vlcg>	B6N(Cg)-Zzef1<tm2.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763859	M	MP:0030610	absent teeth	Zzef1<tm2.1(KOMP)Vlcg>/Zzef1<tm2.1(KOMP)Vlcg>	B6N(Cg)-Zzef1<tm2.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763859	M	MP:0003063	increased coping response	Zzef1<tm2.1(KOMP)Vlcg>/Zzef1<tm2.1(KOMP)Vlcg>	B6N(Cg)-Zzef1<tm2.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5763859	F	MP:0001258	decreased body length	Zzef1<tm2.1(KOMP)Vlcg>/Zzef1<tm2.1(KOMP)Vlcg>	B6N(Cg)-Zzef1<tm2.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5766061	M	MP:0001925	male infertility	Nkapl<tm1(KOMP)Vlcg>/Nkapl<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25875095
MGI:5766061	M	MP:0001147	small testis	Nkapl<tm1(KOMP)Vlcg>/Nkapl<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25875095
MGI:5766061	M	MP:0005159	azoospermia	Nkapl<tm1(KOMP)Vlcg>/Nkapl<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25875095
MGI:5766061	M	MP:0008261	arrest of male meiosis	Nkapl<tm1(KOMP)Vlcg>/Nkapl<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25875095
MGI:5766061	M	MP:0014052	increased male germ cell apoptosis	Nkapl<tm1(KOMP)Vlcg>/Nkapl<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25875095
MGI:5766068	M	MP:0001925	male infertility	Morc1<Tg(Tyr)1Az>/Morc1<Tg(Tyr)1Az>	involves: C57BL/6N * FVB/N	N	26275923
MGI:5766068	F	MP:0003360	abnormal depression-related behavior	Morc1<Tg(Tyr)1Az>/Morc1<Tg(Tyr)1Az>	involves: C57BL/6N * FVB/N	N	26275923
MGI:5766068	F	MP:0005386	behavior/neurological phenotype	Morc1<Tg(Tyr)1Az>/Morc1<Tg(Tyr)1Az>	involves: C57BL/6N * FVB/N	Y	26275923
MGI:5766068	M	MP:0001147	small testis	Morc1<Tg(Tyr)1Az>/Morc1<Tg(Tyr)1Az>	involves: C57BL/6N * FVB/N	N	26275923
MGI:5766290	F	MP:0005379	endocrine/exocrine gland phenotype	Galr3<tm1Lex>/Galr3<tm1Lex>	B6.129S5-Galr3<tm1Lex>	Y	24782539
MGI:5766290	M	MP:0005376	homeostasis/metabolism phenotype	Galr3<tm1Lex>/Galr3<tm1Lex>	B6.129S5-Galr3<tm1Lex>	Y	24782539
MGI:5766290	M	MP:0005386	behavior/neurological phenotype	Galr3<tm1Lex>/Galr3<tm1Lex>	B6.129S5-Galr3<tm1Lex>	Y	24782539
MGI:5766290	M	MP:0005397	hematopoietic system phenotype	Galr3<tm1Lex>/Galr3<tm1Lex>	B6.129S5-Galr3<tm1Lex>	Y	24782539
MGI:5766290	M	MP:0001363	increased anxiety-related response	Galr3<tm1Lex>/Galr3<tm1Lex>	B6.129S5-Galr3<tm1Lex>	N	24782539
MGI:5766290	M	MP:0001402	decreased locomotor activity	Galr3<tm1Lex>/Galr3<tm1Lex>	B6.129S5-Galr3<tm1Lex>	N	24782539
MGI:5766290	M	MP:0001360	abnormal social investigation	Galr3<tm1Lex>/Galr3<tm1Lex>	B6.129S5-Galr3<tm1Lex>	N	24782539
MGI:5766495	M	MP:0002079	increased circulating insulin level	Snap25<tm1.1Bark>/Snap25<tm1.1Bark>	Not Specified	N	26195742
MGI:5766495	M	MP:0005331	insulin resistance	Snap25<tm1.1Bark>/Snap25<tm1.1Bark>	Not Specified	N	26195742
MGI:5766495	M	MP:0011940	decreased food intake	Snap25<tm1.1Bark>/Snap25<tm1.1Bark>	Not Specified	N	26195742
MGI:5766504	M	MP:0004933	abnormal epididymis epithelium morphology	Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>/Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>	Not Specified	N	25759215
MGI:5766504	M	MP:0013600	testis degeneration	Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>/Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>	Not Specified	N	25759215
MGI:5766504	M	MP:0014187	spermatocele	Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>/Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>	Not Specified	N	25759215
MGI:5766504	M	MP:0002631	abnormal epididymis morphology	Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>/Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>	Not Specified	N	25759215
MGI:5766504	M	MP:0002216	abnormal seminiferous tubule morphology	Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>/Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>	Not Specified	N	25759215
MGI:5766504	M	MP:0014186	epididymis hypertrophy	Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>/Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>	Not Specified	N	25759215
MGI:5766504	M	MP:0003596	epididymis inflammation	Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>/Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>	Not Specified	N	25759215
MGI:5766504	M	MP:0014188	epididymis fibrosis	Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>/Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>	Not Specified	N	25759215
MGI:5766504	M	MP:0014192	increased epididymal cell proliferation	Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>/Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>	Not Specified	N	25759215
MGI:5766504	M	MP:0014194	increased epididymal epithelium cell proliferation	Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>/Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>	Not Specified	N	25759215
MGI:5766504	M	MP:0001925	male infertility	Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>/Gt(ROSA)26Sor<tm1.1(Loxl2)Acan>	Not Specified	N	25759215
MGI:5766938	F	MP:0008868	abnormal granulosa cell morphology	Mex3b<tm1.2Mbld>/Mex3b<tm1.2Mbld>	involves: C57BL/6 * CBA	N	24803656
MGI:5766938	M	MP:0002776	increased Sertoli cell number	Mex3b<tm1.2Mbld>/Mex3b<tm1.2Mbld>	involves: C57BL/6 * CBA	N	24803656
MGI:5766938	M	MP:0009853	decreased Sertoli cell phagocytosis	Mex3b<tm1.2Mbld>/Mex3b<tm1.2Mbld>	involves: C57BL/6 * CBA	N	24803656
MGI:5766938	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Mex3b<tm1.2Mbld>/Mex3b<tm1.2Mbld>	involves: C57BL/6 * CBA	N	24803656
MGI:5766938	M	MP:0002687	oligozoospermia	Mex3b<tm1.2Mbld>/Mex3b<tm1.2Mbld>	involves: C57BL/6 * CBA	N	24803656
MGI:5766938	M	MP:0020355	abnormal Sertoli cell barrier morphology	Mex3b<tm1.2Mbld>/Mex3b<tm1.2Mbld>	involves: C57BL/6 * CBA	N	24803656
MGI:5766938	M	MP:0002216	abnormal seminiferous tubule morphology	Mex3b<tm1.2Mbld>/Mex3b<tm1.2Mbld>	involves: C57BL/6 * CBA	N	24803656
MGI:5766938	M	MP:0020356	abnormal Sertoli cell barrier function	Mex3b<tm1.2Mbld>/Mex3b<tm1.2Mbld>	involves: C57BL/6 * CBA	N	24803656
MGI:5766943	M	MP:0020142	increased anti-sperm antibody level	Mex3b<tm1.1Mbld>/Mex3b<tm1.1Mbld>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: C57BL/6 * SJL	N	24803656
MGI:5766943	M	MP:0020356	abnormal Sertoli cell barrier function	Mex3b<tm1.1Mbld>/Mex3b<tm1.1Mbld>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: C57BL/6 * SJL	N	24803656
MGI:5766943	M	MP:0001922	reduced male fertility	Mex3b<tm1.1Mbld>/Mex3b<tm1.1Mbld>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: C57BL/6 * SJL	N	24803656
MGI:5766943	M	MP:0002776	increased Sertoli cell number	Mex3b<tm1.1Mbld>/Mex3b<tm1.1Mbld>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: C57BL/6 * SJL	N	24803656
MGI:5766943	M	MP:0002216	abnormal seminiferous tubule morphology	Mex3b<tm1.1Mbld>/Mex3b<tm1.1Mbld>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: C57BL/6 * SJL	N	24803656
MGI:5767002	M	MP:0003666	impaired sperm capacitation	Rnase9<tm1.1Xen>/Rnase9<tm1.1Xen>	involves: 129S6/SvEvTac	N	24719258
MGI:5767002	M	MP:0002674	abnormal sperm motility	Rnase9<tm1.1Xen>/Rnase9<tm1.1Xen>	involves: 129S6/SvEvTac	N	24719258
MGI:5767140	M	MP:0006320	abnormal interscapular fat pad morphology	Ap1s2<tm1Pschu>/Y	involves: 129P2/OlaHsd * C57BL/6	N	24928897
MGI:5767140	M	MP:0009289	decreased epididymal fat pad weight	Ap1s2<tm1Pschu>/Y	involves: 129P2/OlaHsd * C57BL/6	N	24928897
MGI:5767140	M	MP:0011174	lipodystrophy	Ap1s2<tm1Pschu>/Y	involves: 129P2/OlaHsd * C57BL/6	N	24928897
MGI:5767140	M	MP:0010025	decreased total body fat amount	Ap1s2<tm1Pschu>/Y	involves: 129P2/OlaHsd * C57BL/6	N	24928897
MGI:5767140	M	MP:0011167	abnormal adipose tissue development	Ap1s2<tm1Pschu>/Y	involves: 129P2/OlaHsd * C57BL/6	N	24928897
MGI:5767140	M	MP:0005376	homeostasis/metabolism phenotype	Ap1s2<tm1Pschu>/Y	involves: 129P2/OlaHsd * C57BL/6	Y	24928897
MGI:5767140	M	MP:0008844	decreased subcutaneous adipose tissue amount	Ap1s2<tm1Pschu>/Y	involves: 129P2/OlaHsd * C57BL/6	N	24928897
MGI:5767140	M	MP:0001262	decreased body weight	Ap1s2<tm1Pschu>/Y	involves: 129P2/OlaHsd * C57BL/6	N	24928897
MGI:5767292	M	MP:0004875	increased mean systemic arterial blood pressure	P2ry14<tm1.1Shbg>/P2ry14<tm1.1Shbg>	involves: 129S6/SvEvTac * C57BL/6	N	24993824
MGI:5767292	M	MP:0002727	decreased circulating insulin level	P2ry14<tm1.1Shbg>/P2ry14<tm1.1Shbg>	involves: 129S6/SvEvTac * C57BL/6	N	24993824
MGI:5767292	F	MP:0002335	decreased airway responsiveness	P2ry14<tm1.1Shbg>/P2ry14<tm1.1Shbg>	involves: 129S6/SvEvTac * C57BL/6	N	24993824
MGI:5767292	M	MP:0010182	decreased susceptibility to weight gain	P2ry14<tm1.1Shbg>/P2ry14<tm1.1Shbg>	involves: 129S6/SvEvTac * C57BL/6	N	24993824
MGI:5767292	M	MP:0006144	increased systemic arterial systolic blood pressure	P2ry14<tm1.1Shbg>/P2ry14<tm1.1Shbg>	involves: 129S6/SvEvTac * C57BL/6	N	24993824
MGI:5767292	M	MP:0005293	impaired glucose tolerance	P2ry14<tm1.1Shbg>/P2ry14<tm1.1Shbg>	involves: 129S6/SvEvTac * C57BL/6	N	24993824
MGI:5767292	M	MP:0002626	increased heart rate	P2ry14<tm1.1Shbg>/P2ry14<tm1.1Shbg>	involves: 129S6/SvEvTac * C57BL/6	N	24993824
MGI:5767292	F	MP:0010895	increased lung compliance	P2ry14<tm1.1Shbg>/P2ry14<tm1.1Shbg>	involves: 129S6/SvEvTac * C57BL/6	N	24993824
MGI:5767292	M	MP:0006143	increased systemic arterial diastolic blood pressure	P2ry14<tm1.1Shbg>/P2ry14<tm1.1Shbg>	involves: 129S6/SvEvTac * C57BL/6	N	24993824
MGI:5767545	M	MP:0002152	abnormal brain morphology	Fmc1<tm1b(EUCOMM)Wtsi>/Fmc1<+>	C57BL/6N-Fmc1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767547	F	MP:0003717	pallor	Bltp1<tm1b(EUCOMM)Hmgu>/Bltp1<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Bltp1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5767547	F	MP:0003984	embryonic growth retardation	Bltp1<tm1b(EUCOMM)Hmgu>/Bltp1<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Bltp1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5767547	F	MP:0001697	abnormal embryo size	Bltp1<tm1b(EUCOMM)Hmgu>/Bltp1<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Bltp1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5767548	M	MP:0001944	abnormal pancreas morphology	4933430I17Rik<tm1a(EUCOMM)Wtsi>/4933430I17Rik<tm1a(EUCOMM)Wtsi>	C57BL/6N-4933430I17Rik<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5767548	M	MP:0002590	increased mean corpuscular volume	4933430I17Rik<tm1a(EUCOMM)Wtsi>/4933430I17Rik<tm1a(EUCOMM)Wtsi>	C57BL/6N-4933430I17Rik<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5767549	M	MP:0004931	enlarged epididymis	Scart2<tm1b(KOMP)Wtsi>/Scart2<tm1b(KOMP)Wtsi>	C57BL/6N-A<tm1Brd> Scart2<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:5767549	M	MP:0002631	abnormal epididymis morphology	Scart2<tm1b(KOMP)Wtsi>/Scart2<tm1b(KOMP)Wtsi>	C57BL/6N-A<tm1Brd> Scart2<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:5767552	F	MP:0009142	decreased prepulse inhibition	Abcb9<tm1b(KOMP)Wtsi>/Abcb9<tm1b(KOMP)Wtsi>	C57BL/6N-Abcb9<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5767552	M	MP:0002768	small adrenal glands	Abcb9<tm1b(KOMP)Wtsi>/Abcb9<tm1b(KOMP)Wtsi>	C57BL/6N-Abcb9<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5767552	M	MP:0010052	increased grip strength	Abcb9<tm1b(KOMP)Wtsi>/Abcb9<tm1b(KOMP)Wtsi>	C57BL/6N-Abcb9<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5767552	M	MP:0000702	enlarged lymph nodes	Abcb9<tm1b(KOMP)Wtsi>/Abcb9<tm1b(KOMP)Wtsi>	C57BL/6N-Abcb9<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5767553	F	MP:0003019	increased circulating chloride level	Acat2<tm1b(KOMP)Wtsi>/Acat2<+>	C57BL/6N-Acat2<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767555	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Ackr3<tm2b(EUCOMM)Wtsi>/Ackr3<+>	C57BL/6N-Ackr3<tm2b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5767555	M	MP:0010053	decreased grip strength	Ackr3<tm2b(EUCOMM)Wtsi>/Ackr3<+>	C57BL/6N-Ackr3<tm2b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5767558	M	MP:0000706	small thymus	Aif1l<tm1b(EUCOMM)Wtsi>/Aif1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aif1l<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767558	F	MP:0000689	abnormal spleen morphology	Aif1l<tm1b(EUCOMM)Wtsi>/Aif1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aif1l<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767558	F	MP:0003731	abnormal retina outer nuclear layer morphology	Aif1l<tm1b(EUCOMM)Wtsi>/Aif1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aif1l<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767558	M	MP:0000598	abnormal liver morphology	Aif1l<tm1b(EUCOMM)Wtsi>/Aif1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aif1l<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767558	M	MP:0002060	abnormal skin morphology	Aif1l<tm1b(EUCOMM)Wtsi>/Aif1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aif1l<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767558	M	MP:0000691	enlarged spleen	Aif1l<tm1b(EUCOMM)Wtsi>/Aif1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aif1l<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767558	M	MP:0004952	increased spleen weight	Aif1l<tm1b(EUCOMM)Wtsi>/Aif1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aif1l<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767559	M	MP:0002874	decreased hemoglobin content	Aldh9a1<tm1b(KOMP)Wtsi>/Aldh9a1<tm1b(KOMP)Wtsi>	C57BL/6N-Aldh9a1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767559	M	MP:0002060	abnormal skin morphology	Aldh9a1<tm1b(KOMP)Wtsi>/Aldh9a1<tm1b(KOMP)Wtsi>	C57BL/6N-Aldh9a1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767562	F	MP:0001333	absent optic nerve	Angptl4<tm1b(EUCOMM)Hmgu>/Angptl4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Angptl4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5767562	M	MP:0002644	decreased circulating triglyceride level	Angptl4<tm1b(EUCOMM)Hmgu>/Angptl4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Angptl4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5767565	M	MP:0005179	decreased circulating cholesterol level	Apoc4<tm1.1(KOMP)Mbp>/Apoc4<tm1.1(KOMP)Mbp>	C57BL/6N-Apoc4<tm1.1(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:5767565	M	MP:0002941	increased circulating alanine transaminase level	Apoc4<tm1.1(KOMP)Mbp>/Apoc4<tm1.1(KOMP)Mbp>	C57BL/6N-Apoc4<tm1.1(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:5767565	F	MP:0002968	increased circulating alkaline phosphatase level	Apoc4<tm1.1(KOMP)Mbp>/Apoc4<tm1.1(KOMP)Mbp>	C57BL/6N-Apoc4<tm1.1(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:5767565	F	MP:0003020	decreased circulating chloride level	Apoc4<tm1.1(KOMP)Mbp>/Apoc4<tm1.1(KOMP)Mbp>	C57BL/6N-Apoc4<tm1.1(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:5767567	M	MP:0002608	increased hematocrit	Arhgef1<tm1a(EUCOMM)Wtsi>/Arhgef1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arhgef1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767567	F	MP:0005564	increased hemoglobin content	Arhgef1<tm1a(EUCOMM)Wtsi>/Arhgef1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arhgef1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767567	M	MP:0010838	increased CD8-positive, alpha-beta memory T cell number	Arhgef1<tm1a(EUCOMM)Wtsi>/Arhgef1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arhgef1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767569	M	MP:0005419	decreased circulating serum albumin level	Arl5c<tm1.1(KOMP)Vlcg>/Arl5c<tm1.1(KOMP)Vlcg>	C57BL/6N-Arl5c<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767569	M	MP:0000195	decreased circulating calcium level	Arl5c<tm1.1(KOMP)Vlcg>/Arl5c<tm1.1(KOMP)Vlcg>	C57BL/6N-Arl5c<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767569	F	MP:0000274	enlarged heart	Arl5c<tm1.1(KOMP)Vlcg>/Arl5c<tm1.1(KOMP)Vlcg>	C57BL/6N-Arl5c<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767569	M	MP:0005567	decreased circulating total protein level	Arl5c<tm1.1(KOMP)Vlcg>/Arl5c<tm1.1(KOMP)Vlcg>	C57BL/6N-Arl5c<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767569	F	MP:0000266	abnormal heart morphology	Arl5c<tm1.1(KOMP)Vlcg>/Arl5c<tm1.1(KOMP)Vlcg>	C57BL/6N-Arl5c<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767569	F	MP:0002152	abnormal brain morphology	Arl5c<tm1.1(KOMP)Vlcg>/Arl5c<tm1.1(KOMP)Vlcg>	C57BL/6N-Arl5c<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767569	F	MP:0001891	hydrocephaly	Arl5c<tm1.1(KOMP)Vlcg>/Arl5c<tm1.1(KOMP)Vlcg>	C57BL/6N-Arl5c<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767569	M	MP:0005554	decreased circulating creatinine level	Arl5c<tm1.1(KOMP)Vlcg>/Arl5c<tm1.1(KOMP)Vlcg>	C57BL/6N-Arl5c<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767582	M	MP:0001147	small testis	Blk<tm1.1(KOMP)Vlcg>/Blk<tm1.1(KOMP)Vlcg>	C57BL/6N-Blk<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767582	M	MP:0001146	abnormal testis morphology	Blk<tm1.1(KOMP)Vlcg>/Blk<tm1.1(KOMP)Vlcg>	C57BL/6N-Blk<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767583	M	MP:0011100	preweaning lethality, complete penetrance	Bmi1<tm1.1(KOMP)Vlcg>/Bmi1<tm1.1(KOMP)Vlcg>	C57BL/6N-Bmi1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767584	F	MP:0005566	decreased blood urea nitrogen level	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	F	MP:0003795	abnormal bone structure	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	M	MP:0005560	decreased circulating glucose level	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	F	MP:0001926	female infertility	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	M	MP:0001925	male infertility	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	F	MP:0001258	decreased body length	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	F	MP:0000218	increased leukocyte cell number	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	M	MP:0000186	decreased circulating HDL cholesterol level	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	M	MP:0001304	cataract	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	M	MP:0003019	increased circulating chloride level	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	F	MP:0008346	increased gamma-delta T cell number	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	F	MP:0000219	increased neutrophil cell number	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	M	MP:0005633	increased circulating sodium level	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	M	MP:0001303	abnormal lens morphology	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767584	M	MP:0003443	increased circulating glycerol level	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767586	M	MP:0011100	preweaning lethality, complete penetrance	Ccdc39<tm2b(KOMP)Wtsi>/Ccdc39<tm2b(KOMP)Wtsi>	C57BL/6N-Ccdc39<tm2b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5767588	M	MP:0000266	abnormal heart morphology	Cd83<tm1b(KOMP)Wtsi>/Cd83<tm1b(KOMP)Wtsi>	C57BL/6N-Cd83<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767588	M	MP:0000274	enlarged heart	Cd83<tm1b(KOMP)Wtsi>/Cd83<tm1b(KOMP)Wtsi>	C57BL/6N-Cd83<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767589	F	MP:0011100	preweaning lethality, complete penetrance	Cdan1<tm1b(KOMP)Wtsi>/Cdan1<tm1b(KOMP)Wtsi>	C57BL/6N-Cdan1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767591	M	MP:0005628	decreased circulating potassium level	Cdkl2<tm1b(EUCOMM)Hmgu>/Cdkl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cdkl2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5767591	F	MP:0005632	decreased circulating aspartate transaminase level	Cdkl2<tm1b(EUCOMM)Hmgu>/Cdkl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cdkl2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5767591	M	MP:0010124	decreased bone mineral content	Cdkl2<tm1b(EUCOMM)Hmgu>/Cdkl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cdkl2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5767591	M	MP:0000198	decreased circulating phosphate level	Cdkl2<tm1b(EUCOMM)Hmgu>/Cdkl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cdkl2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5767592	F	MP:0000689	abnormal spleen morphology	Cdkn1a<tm1.1(KOMP)Vlcg>/Cdkn1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Cdkn1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767592	M	MP:0002631	abnormal epididymis morphology	Cdkn1a<tm1.1(KOMP)Vlcg>/Cdkn1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Cdkn1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767592	M	MP:0000266	abnormal heart morphology	Cdkn1a<tm1.1(KOMP)Vlcg>/Cdkn1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Cdkn1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767592	F	MP:0000691	enlarged spleen	Cdkn1a<tm1.1(KOMP)Vlcg>/Cdkn1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Cdkn1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767592	M	MP:0001146	abnormal testis morphology	Cdkn1a<tm1.1(KOMP)Vlcg>/Cdkn1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Cdkn1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767592	M	MP:0004931	enlarged epididymis	Cdkn1a<tm1.1(KOMP)Vlcg>/Cdkn1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Cdkn1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767592	M	MP:0000274	enlarged heart	Cdkn1a<tm1.1(KOMP)Vlcg>/Cdkn1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Cdkn1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767592	M	MP:0001147	small testis	Cdkn1a<tm1.1(KOMP)Vlcg>/Cdkn1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Cdkn1a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767595	F	MP:0003720	abnormal neural tube closure	Cecr2<tm2b(EUCOMM)Hmgu>/Cecr2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Cecr2<tm2b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5767595	F	MP:0000897	abnormal midbrain morphology	Cecr2<tm2b(EUCOMM)Hmgu>/Cecr2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Cecr2<tm2b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5767595	F	MP:0000841	abnormal hindbrain morphology	Cecr2<tm2b(EUCOMM)Hmgu>/Cecr2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Cecr2<tm2b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5767595	F	MP:0000783	abnormal forebrain morphology	Cecr2<tm2b(EUCOMM)Hmgu>/Cecr2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Cecr2<tm2b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5767597	F	MP:0000689	abnormal spleen morphology	Cep76<tm1b(EUCOMM)Hmgu>/Cep76<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cep76<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5767598	M	MP:0008854	bleb	Cep97<tm1.1(KOMP)Vlcg>/Cep97<tm1.1(KOMP)Vlcg>	C57BL/6N-Cep97<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767604	F	MP:0003984	embryonic growth retardation	Cnbp<tm1b(KOMP)Wtsi>/Cnbp<tm1b(KOMP)Wtsi>	B6N(Cg)-Cnbp<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5767605	M	MP:0003984	embryonic growth retardation	Cnnm2<tm1.1(KOMP)Vlcg>/Cnnm2<tm1.1(KOMP)Vlcg>	C57BL/6N-Cnnm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767605	M	MP:0000428	abnormal craniofacial morphology	Cnnm2<tm1.1(KOMP)Vlcg>/Cnnm2<tm1.1(KOMP)Vlcg>	C57BL/6N-Cnnm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767608	M	MP:0002874	decreased hemoglobin content	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767608	F	MP:0002599	increased mean platelet volume	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767608	M	MP:0002875	decreased erythrocyte cell number	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767608	F	MP:0000218	increased leukocyte cell number	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767608	M	MP:0003036	vertebral transformation	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767608	F	MP:0005344	increased circulating bilirubin level	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767608	F	MP:0001312	abnormal cornea morphology	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767608	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767608	F	MP:0010067	increased red blood cell distribution width	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767608	F	MP:0013022	increased Ly6C high monocyte number	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767608	F	MP:0005562	decreased mean corpuscular hemoglobin	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767608	M	MP:0000208	decreased hematocrit	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767608	F	MP:0002075	abnormal coat/hair pigmentation	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767608	M	MP:0013157	increased KLRG1+ CD4 alpha-beta T cell number	Cog6<tm1a(EUCOMM)Wtsi>/Cog6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cog6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767609	M	MP:0005633	increased circulating sodium level	Coq6<tm1b(EUCOMM)Hmgu>/Coq6<+>	B6N(Cg)-Coq6<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5767610	F	MP:0002075	abnormal coat/hair pigmentation	Cotl1<tm1b(EUCOMM)Hmgu>/Cotl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cotl1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5767610	F	MP:0000218	increased leukocyte cell number	Cotl1<tm1b(EUCOMM)Hmgu>/Cotl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cotl1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5767612	M	MP:0004576	abnormal embryonic autopod plate morphology	Cox5b<tm2b(EUCOMM)Hmgu>/Cox5b<tm2b(EUCOMM)Hmgu>	C57BL/6N-Cox5b<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5767612	M	MP:0003717	pallor	Cox5b<tm2b(EUCOMM)Hmgu>/Cox5b<tm2b(EUCOMM)Hmgu>	C57BL/6N-Cox5b<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5767612	M	MP:0000603	pale liver	Cox5b<tm2b(EUCOMM)Hmgu>/Cox5b<tm2b(EUCOMM)Hmgu>	C57BL/6N-Cox5b<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5767612	M	MP:0004848	abnormal liver size	Cox5b<tm2b(EUCOMM)Hmgu>/Cox5b<tm2b(EUCOMM)Hmgu>	C57BL/6N-Cox5b<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5767615	M	MP:0005562	decreased mean corpuscular hemoglobin	Cript<tm1.1(KOMP)Vlcg>/Cript<+>	B6N(Cg)-Cript<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5767619	M	MP:0000689	abnormal spleen morphology	Cyp2ab1<tm1b(KOMP)Wtsi>/Cyp2ab1<tm1b(KOMP)Wtsi>	C57BL/6N-Cyp2ab1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767619	F	MP:0000198	decreased circulating phosphate level	Cyp2ab1<tm1b(KOMP)Wtsi>/Cyp2ab1<tm1b(KOMP)Wtsi>	C57BL/6N-Cyp2ab1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767620	F	MP:0003795	abnormal bone structure	Cyp2u1<tm1b(EUCOMM)Wtsi>/Cyp2u1<tm1b(EUCOMM)Wtsi>	B6N(Cg)-Cyp2u1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5767621	F	MP:0002792	abnormal retina vasculature morphology	Cyp4f14<tm1b(EUCOMM)Hmgu>/Cyp4f14<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp4f14<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5767621	F	MP:0010097	abnormal retina blood vessel morphology	Cyp4f14<tm1b(EUCOMM)Hmgu>/Cyp4f14<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp4f14<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5767624	M	MP:0005179	decreased circulating cholesterol level	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767624	M	MP:0000274	enlarged heart	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767624	M	MP:0005419	decreased circulating serum albumin level	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767625	F	MP:0010506	prolonged RR interval	Dcps<tm1b(EUCOMM)Hmgu>/Dcps<+>	B6N(Cg)-Dcps<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5767628	M	MP:0009142	decreased prepulse inhibition	Dennd2d<tm2b(KOMP)Mbp>/Dennd2d<tm2b(KOMP)Mbp>	C57BL/6N-Dennd2d<tm2b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5767630	F	MP:0010123	increased bone mineral content	Dgcr2<tm1b(EUCOMM)Wtsi>/Dgcr2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dgcr2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767630	F	MP:0000689	abnormal spleen morphology	Dgcr2<tm1b(EUCOMM)Wtsi>/Dgcr2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dgcr2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767635	M	MP:0011100	preweaning lethality, complete penetrance	Dnah5<tm1b(KOMP)Wtsi>/Dnah5<tm1b(KOMP)Wtsi>	C57BL/6N-Dnah5<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767642	F	MP:0000266	abnormal heart morphology	Dpf2<tm1b(EUCOMM)Hmgu>/Dpf2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dpf2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5767647	F	MP:0003984	embryonic growth retardation	Ehmt2<tm1.1(KOMP)Mbp>/Ehmt2<tm1.1(KOMP)Mbp>	C57BL/6N-Ehmt2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5767649	F	MP:0008806	increased circulating amylase level	Elovl6<tm1b(EUCOMM)Hmgu>/Elovl6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elovl6<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5767649	F	MP:0002968	increased circulating alkaline phosphatase level	Elovl6<tm1b(EUCOMM)Hmgu>/Elovl6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elovl6<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5767649	F	MP:0001513	limb grasping	Elovl6<tm1b(EUCOMM)Hmgu>/Elovl6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elovl6<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5767649	F	MP:0001552	increased circulating triglyceride level	Elovl6<tm1b(EUCOMM)Hmgu>/Elovl6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elovl6<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5767654	M	MP:0001175	abnormal lung morphology	Eprs1<tm1b(EUCOMM)Hmgu>/Eprs1<+>	C57BL/6N-Eprs1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5767657	M	MP:0000062	increased bone mineral density	Etnk1<tm1b(EUCOMM)Wtsi>/Etnk1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Etnk1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767657	F	MP:0000689	abnormal spleen morphology	Etnk1<tm1b(EUCOMM)Wtsi>/Etnk1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Etnk1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767663	F	MP:0000689	abnormal spleen morphology	Fbxw9<tm1b(EUCOMM)Wtsi>/Fbxw9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fbxw9<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767667	M	MP:0003984	embryonic growth retardation	Fitm2<tm1.1(KOMP)Vlcg>/Fitm2<tm1.1(KOMP)Vlcg>	C57BL/6N-Fitm2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5767667	M	MP:0000288	abnormal pericardium morphology	Fitm2<tm1.1(KOMP)Vlcg>/Fitm2<tm1.1(KOMP)Vlcg>	C57BL/6N-Fitm2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5767670	F	MP:0011100	preweaning lethality, complete penetrance	Fscn1<tm1.1(KOMP)Vlcg>/Fscn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fscn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767677	F	MP:0000689	abnormal spleen morphology	Gnai1<tm1b(EUCOMM)Wtsi>/Gnai1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gnai1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767678	F	MP:0001120	abnormal uterus morphology	Gnpda1<tm1b(KOMP)Mbp>/Gnpda1<+>	C57BL/6N-Gnpda1<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5767678	M	MP:0000219	increased neutrophil cell number	Gnpda1<tm1b(KOMP)Mbp>/Gnpda1<+>	C57BL/6N-Gnpda1<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5767678	F	MP:0002989	small kidney	Gnpda1<tm1b(KOMP)Mbp>/Gnpda1<+>	C57BL/6N-Gnpda1<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5767679	F	MP:0003984	embryonic growth retardation	Golga7<tm1b(KOMP)Wtsi>/Golga7<tm1b(KOMP)Wtsi>	C57BL/6N-Golga7<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767679	F	MP:0001697	abnormal embryo size	Golga7<tm1b(KOMP)Wtsi>/Golga7<tm1b(KOMP)Wtsi>	C57BL/6N-Golga7<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767688	M	MP:0001147	small testis	Hsf2bp<tm1b(EUCOMM)Hmgu>/Hsf2bp<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hsf2bp<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5767688	F	MP:0000702	enlarged lymph nodes	Hsf2bp<tm1b(EUCOMM)Hmgu>/Hsf2bp<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hsf2bp<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5767689	M	MP:0000274	enlarged heart	Ifi204<tm1b(KOMP)Wtsi>/Ifi204<tm1b(KOMP)Wtsi>	C57BL/6N-Ifi204<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767705	F	MP:0005287	narrow eye opening	Kntc1<tm1b(EUCOMM)Hmgu>/Kntc1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kntc1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5767706	F	MP:0000266	abnormal heart morphology	Krit1<tm1.1(KOMP)Vlcg>/Krit1<+>	C57BL/6N-Krit1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767706	M	MP:0010053	decreased grip strength	Krit1<tm1.1(KOMP)Vlcg>/Krit1<+>	C57BL/6N-Krit1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767706	F	MP:0002092	abnormal eye morphology	Krit1<tm1.1(KOMP)Vlcg>/Krit1<+>	C57BL/6N-Krit1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767706	M	MP:0002941	increased circulating alanine transaminase level	Krit1<tm1.1(KOMP)Vlcg>/Krit1<+>	C57BL/6N-Krit1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767706	F	MP:0000274	enlarged heart	Krit1<tm1.1(KOMP)Vlcg>/Krit1<+>	C57BL/6N-Krit1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767706	F	MP:0001333	absent optic nerve	Krit1<tm1.1(KOMP)Vlcg>/Krit1<+>	C57BL/6N-Krit1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767707	F	MP:0011100	preweaning lethality, complete penetrance	Krt5<tm1.1(KOMP)Vlcg>/Krt5<tm1.1(KOMP)Vlcg>	C57BL/6N-Krt5<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5767710	M	MP:0002135	abnormal kidney morphology	Lancl2<tm2b(KOMP)Wtsi>/Lancl2<tm2b(KOMP)Wtsi>	C57BL/6N-Lancl2<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767710	M	MP:0003068	enlarged kidney	Lancl2<tm2b(KOMP)Wtsi>/Lancl2<tm2b(KOMP)Wtsi>	C57BL/6N-Lancl2<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767710	M	MP:0000274	enlarged heart	Lancl2<tm2b(KOMP)Wtsi>/Lancl2<tm2b(KOMP)Wtsi>	C57BL/6N-Lancl2<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767710	M	MP:0000266	abnormal heart morphology	Lancl2<tm2b(KOMP)Wtsi>/Lancl2<tm2b(KOMP)Wtsi>	C57BL/6N-Lancl2<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767714	F	MP:0011100	preweaning lethality, complete penetrance	Lhx6<tm1b(KOMP)Wtsi>/Lhx6<tm1b(KOMP)Wtsi>	C57BL/6N-Lhx6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767721	M	MP:0001722	pale yolk sac	Med16<tm1b(KOMP)Wtsi>/Med16<tm1b(KOMP)Wtsi>	C57BL/6N-Med16<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767721	M	MP:0000603	pale liver	Med16<tm1b(KOMP)Wtsi>/Med16<tm1b(KOMP)Wtsi>	C57BL/6N-Med16<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767721	M	MP:0004258	abnormal placenta size	Med16<tm1b(KOMP)Wtsi>/Med16<tm1b(KOMP)Wtsi>	C57BL/6N-Med16<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767723	F	MP:0002953	thick ventricular wall	Memo1<tm1b(EUCOMM)Wtsi>/Memo1<+>	C57BL/6N-Memo1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767725	M	MP:0000467	abnormal esophagus morphology	Mgat4d<tm1b(KOMP)Wtsi>/Mgat4d<tm1b(KOMP)Wtsi>	C57BL/6N-Mgat4d<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767726	M	MP:0002176	increased brain weight	Mlc1<tm1.1(KOMP)Vlcg>/Mlc1<tm1.1(KOMP)Vlcg>	C57BL/6N-Mlc1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767726	F	MP:0001120	abnormal uterus morphology	Mlc1<tm1.1(KOMP)Vlcg>/Mlc1<tm1.1(KOMP)Vlcg>	C57BL/6N-Mlc1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767727	F	MP:0000691	enlarged spleen	Mmp15<tm1b(KOMP)Wtsi>/Mmp15<tm1b(KOMP)Wtsi>	C57BL/6N-Mmp15<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767727	F	MP:0011239	abnormal skin coloration	Mmp15<tm1b(KOMP)Wtsi>/Mmp15<tm1b(KOMP)Wtsi>	C57BL/6N-Mmp15<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767727	F	MP:0000195	decreased circulating calcium level	Mmp15<tm1b(KOMP)Wtsi>/Mmp15<tm1b(KOMP)Wtsi>	C57BL/6N-Mmp15<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767727	M	MP:0000467	abnormal esophagus morphology	Mmp15<tm1b(KOMP)Wtsi>/Mmp15<tm1b(KOMP)Wtsi>	C57BL/6N-Mmp15<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767727	M	MP:0000681	abnormal thyroid gland morphology	Mmp15<tm1b(KOMP)Wtsi>/Mmp15<tm1b(KOMP)Wtsi>	C57BL/6N-Mmp15<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767732	M	MP:0002060	abnormal skin morphology	Mthfd2l<tm1b(EUCOMM)Wtsi>/Mthfd2l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Mthfd2l<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5767732	M	MP:0003960	increased lean body mass	Mthfd2l<tm1b(EUCOMM)Wtsi>/Mthfd2l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Mthfd2l<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5767732	M	MP:0000274	enlarged heart	Mthfd2l<tm1b(EUCOMM)Wtsi>/Mthfd2l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Mthfd2l<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5767736	M	MP:0001891	hydrocephaly	Nampt<tm1.1(KOMP)Vlcg>/Nampt<+>	C57BL/6N-Nampt<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767736	M	MP:0002152	abnormal brain morphology	Nampt<tm1.1(KOMP)Vlcg>/Nampt<+>	C57BL/6N-Nampt<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767737	M	MP:0002100	abnormal tooth morphology	Ncoa3<tm1b(EUCOMM)Wtsi>/Ncoa3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ncoa3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5767737	M	MP:0001289	persistence of hyaloid vascular system	Ncoa3<tm1b(EUCOMM)Wtsi>/Ncoa3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ncoa3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5767741	M	MP:0000274	enlarged heart	Nlrp9b<tm1b(KOMP)Wtsi>/Nlrp9b<tm1b(KOMP)Wtsi>	C57BL/6N-Nlrp9b<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5767741	M	MP:0001147	small testis	Nlrp9b<tm1b(KOMP)Wtsi>/Nlrp9b<tm1b(KOMP)Wtsi>	C57BL/6N-Nlrp9b<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5767741	F	MP:0000691	enlarged spleen	Nlrp9b<tm1b(KOMP)Wtsi>/Nlrp9b<tm1b(KOMP)Wtsi>	C57BL/6N-Nlrp9b<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5767745	F	MP:0001120	abnormal uterus morphology	Nphp1<tm1.1(KOMP)Vlcg>/Nphp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nphp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767745	M	MP:0001146	abnormal testis morphology	Nphp1<tm1.1(KOMP)Vlcg>/Nphp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nphp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767745	M	MP:0001925	male infertility	Nphp1<tm1.1(KOMP)Vlcg>/Nphp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nphp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767745	F	MP:0009709	hydrometra	Nphp1<tm1.1(KOMP)Vlcg>/Nphp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nphp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767745	F	MP:0004906	enlarged uterus	Nphp1<tm1.1(KOMP)Vlcg>/Nphp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nphp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767745	M	MP:0001147	small testis	Nphp1<tm1.1(KOMP)Vlcg>/Nphp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nphp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767745	M	MP:0002060	abnormal skin morphology	Nphp1<tm1.1(KOMP)Vlcg>/Nphp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nphp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767762	F	MP:0001785	edema	Pip5k1c<tm1b(KOMP)Wtsi>/Pip5k1c<tm1b(KOMP)Wtsi>	C57BL/6N-Pip5k1c<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5767763	F	MP:0008259	abnormal optic disk morphology	Pitx2<tm1b(EUCOMM)Wtsi>/Pitx2<+>	C57BL/6N-Pitx2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5767763	M	MP:0002100	abnormal tooth morphology	Pitx2<tm1b(EUCOMM)Wtsi>/Pitx2<+>	C57BL/6N-Pitx2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5767763	M	MP:0001147	small testis	Pitx2<tm1b(EUCOMM)Wtsi>/Pitx2<+>	C57BL/6N-Pitx2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5767763	F	MP:0000274	enlarged heart	Pitx2<tm1b(EUCOMM)Wtsi>/Pitx2<+>	C57BL/6N-Pitx2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5767763	F	MP:0010052	increased grip strength	Pitx2<tm1b(EUCOMM)Wtsi>/Pitx2<+>	C57BL/6N-Pitx2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5767765	M	MP:0002833	increased heart weight	Pld1<tm1b(KOMP)Wtsi>/Pld1<tm1b(KOMP)Wtsi>	C57BL/6N-Pld1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767769	M	MP:0000274	enlarged heart	Prelid2<tm1b(EUCOMM)Wtsi>/Prelid2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Prelid2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5767769	M	MP:0003960	increased lean body mass	Prelid2<tm1b(EUCOMM)Wtsi>/Prelid2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Prelid2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5767770	M	MP:0000274	enlarged heart	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767770	M	MP:0011110	preweaning lethality, incomplete penetrance	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767770	F	MP:0003733	abnormal retina inner nuclear layer morphology	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767771	M	MP:0010053	decreased grip strength	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:5767771	F	MP:0011965	decreased total retina thickness	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:5767771	M	MP:0002833	increased heart weight	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:5767771	F	MP:0001293	anophthalmia	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:5767776	F	MP:0001566	increased circulating phosphate level	Ptpdc1<tm1.1(KOMP)Vlcg>/Ptpdc1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpdc1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767776	F	MP:0010124	decreased bone mineral content	Ptpdc1<tm1.1(KOMP)Vlcg>/Ptpdc1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpdc1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767777	F	MP:0002135	abnormal kidney morphology	Ptpn14<tm1.1(KOMP)Vlcg>/Ptpn14<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpn14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767777	F	MP:0001120	abnormal uterus morphology	Ptpn14<tm1.1(KOMP)Vlcg>/Ptpn14<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpn14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767777	F	MP:0000274	enlarged heart	Ptpn14<tm1.1(KOMP)Vlcg>/Ptpn14<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpn14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767777	F	MP:0000266	abnormal heart morphology	Ptpn14<tm1.1(KOMP)Vlcg>/Ptpn14<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpn14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767777	M	MP:0011110	preweaning lethality, incomplete penetrance	Ptpn14<tm1.1(KOMP)Vlcg>/Ptpn14<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpn14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767777	M	MP:0002989	small kidney	Ptpn14<tm1.1(KOMP)Vlcg>/Ptpn14<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpn14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767777	F	MP:0003604	single kidney	Ptpn14<tm1.1(KOMP)Vlcg>/Ptpn14<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpn14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767777	F	MP:0003960	increased lean body mass	Ptpn14<tm1.1(KOMP)Vlcg>/Ptpn14<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpn14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767777	F	MP:0004906	enlarged uterus	Ptpn14<tm1.1(KOMP)Vlcg>/Ptpn14<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpn14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767777	M	MP:0001925	male infertility	Ptpn14<tm1.1(KOMP)Vlcg>/Ptpn14<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpn14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767777	F	MP:0009709	hydrometra	Ptpn14<tm1.1(KOMP)Vlcg>/Ptpn14<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpn14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767784	M	MP:0006203	eye hemorrhage	Rbp4<tm1.1(KOMP)Vlcg>/Rbp4<tm1.1(KOMP)Vlcg>	C57BL/6N-Rbp4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767784	F	MP:0005561	increased mean corpuscular hemoglobin	Rbp4<tm1.1(KOMP)Vlcg>/Rbp4<tm1.1(KOMP)Vlcg>	C57BL/6N-Rbp4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767792	F	MP:0011100	preweaning lethality, complete penetrance	S100a6<tm1b(KOMP)Wtsi>/S100a6<tm1b(KOMP)Wtsi>	C57BL/6N-S100a6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5767798	F	MP:0000689	abnormal spleen morphology	Serpinf1<tm1e.1(KOMP)Wtsi>/Serpinf1<tm1e.1(KOMP)Wtsi>	C57BL/6N-Serpinf1<tm1e.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767800	M	MP:0002060	abnormal skin morphology	Slc17a9<tm1.1(KOMP)Vlcg>/Slc17a9<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc17a9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767800	F	MP:0002092	abnormal eye morphology	Slc17a9<tm1.1(KOMP)Vlcg>/Slc17a9<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc17a9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767801	M	MP:0000274	enlarged heart	Slc25a3<tm1b(EUCOMM)Wtsi>/Slc25a3<+>	C57BL/6N-Slc25a3<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5767801	M	MP:0000266	abnormal heart morphology	Slc25a3<tm1b(EUCOMM)Wtsi>/Slc25a3<+>	C57BL/6N-Slc25a3<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5767801	M	MP:0001147	small testis	Slc25a3<tm1b(EUCOMM)Wtsi>/Slc25a3<+>	C57BL/6N-Slc25a3<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5767802	F	MP:0003864	abnormal midbrain development	Slc35b4<tm1.1(KOMP)Vlcg>/Slc35b4<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc35b4<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5767802	F	MP:0003720	abnormal neural tube closure	Slc35b4<tm1.1(KOMP)Vlcg>/Slc35b4<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc35b4<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5767802	F	MP:0006108	abnormal hindbrain development	Slc35b4<tm1.1(KOMP)Vlcg>/Slc35b4<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc35b4<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5767802	F	MP:0003232	abnormal forebrain development	Slc35b4<tm1.1(KOMP)Vlcg>/Slc35b4<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc35b4<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5767806	F	MP:0005561	increased mean corpuscular hemoglobin	Slc6a14<tm1b(KOMP)Wtsi>/Slc6a14<tm1b(KOMP)Wtsi>	C57BL/6N-Slc6a14<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5767806	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Slc6a14<tm1b(KOMP)Wtsi>/Slc6a14<tm1b(KOMP)Wtsi>	C57BL/6N-Slc6a14<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5767812	F	MP:0004952	increased spleen weight	Spo11<tm2b(KOMP)Wtsi>/Spo11<tm2b(KOMP)Wtsi>	C57BL/6N-Spo11<tm2b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5767819	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Supt4a<tm1b(EUCOMM)Hmgu>/Supt4a<+>	C57BL/6N-Supt4a<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5767822	M	MP:0002546	mydriasis	Catsperz<tm1.1(KOMP)Vlcg>/Catsperz<tm1.1(KOMP)Vlcg>	B6N(Cg)-Catsperz<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5767822	M	MP:0010124	decreased bone mineral content	Catsperz<tm1.1(KOMP)Vlcg>/Catsperz<tm1.1(KOMP)Vlcg>	B6N(Cg)-Catsperz<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5767822	M	MP:0002833	increased heart weight	Catsperz<tm1.1(KOMP)Vlcg>/Catsperz<tm1.1(KOMP)Vlcg>	B6N(Cg)-Catsperz<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5767827	F	MP:0005013	increased lymphocyte cell number	Tmem100<tm1e.1(KOMP)Wtsi>/Tmem100<+>	C57BL/6N-Tmem100<tm1e.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5767827	M	MP:0000195	decreased circulating calcium level	Tmem100<tm1e.1(KOMP)Wtsi>/Tmem100<+>	C57BL/6N-Tmem100<tm1e.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5767827	F	MP:0000218	increased leukocyte cell number	Tmem100<tm1e.1(KOMP)Wtsi>/Tmem100<+>	C57BL/6N-Tmem100<tm1e.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5767827	F	MP:0001175	abnormal lung morphology	Tmem100<tm1e.1(KOMP)Wtsi>/Tmem100<+>	C57BL/6N-Tmem100<tm1e.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5767829	M	MP:0002631	abnormal epididymis morphology	Tmem174<tm1.1(KOMP)Vlcg>/Tmem174<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem174<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767829	M	MP:0004931	enlarged epididymis	Tmem174<tm1.1(KOMP)Vlcg>/Tmem174<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem174<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767833	F	MP:0010097	abnormal retina blood vessel morphology	Trmt1<tm1b(EUCOMM)Hmgu>/Trmt1<+>	C57BL/6N-Trmt1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5767833	F	MP:0010392	prolonged QRS complex duration	Trmt1<tm1b(EUCOMM)Hmgu>/Trmt1<+>	C57BL/6N-Trmt1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5767833	F	MP:0000598	abnormal liver morphology	Trmt1<tm1b(EUCOMM)Hmgu>/Trmt1<+>	C57BL/6N-Trmt1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5767833	M	MP:0005179	decreased circulating cholesterol level	Trmt1<tm1b(EUCOMM)Hmgu>/Trmt1<+>	C57BL/6N-Trmt1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5767833	M	MP:0002590	increased mean corpuscular volume	Trmt1<tm1b(EUCOMM)Hmgu>/Trmt1<+>	C57BL/6N-Trmt1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5767833	F	MP:0002792	abnormal retina vasculature morphology	Trmt1<tm1b(EUCOMM)Hmgu>/Trmt1<+>	C57BL/6N-Trmt1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5767833	F	MP:0002135	abnormal kidney morphology	Trmt1<tm1b(EUCOMM)Hmgu>/Trmt1<+>	C57BL/6N-Trmt1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5767835	F	MP:0010052	increased grip strength	Tst<tm1.1(KOMP)Vlcg>/Tst<tm1.1(KOMP)Vlcg>	C57BL/6N-Tst<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767835	F	MP:0001258	decreased body length	Tst<tm1.1(KOMP)Vlcg>/Tst<tm1.1(KOMP)Vlcg>	C57BL/6N-Tst<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767835	M	MP:0002631	abnormal epididymis morphology	Tst<tm1.1(KOMP)Vlcg>/Tst<tm1.1(KOMP)Vlcg>	C57BL/6N-Tst<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767835	M	MP:0002590	increased mean corpuscular volume	Tst<tm1.1(KOMP)Vlcg>/Tst<tm1.1(KOMP)Vlcg>	C57BL/6N-Tst<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767836	F	MP:0000218	increased leukocyte cell number	Tst<tm1(KOMP)Vlcg>/Tst<tm1(KOMP)Vlcg>	C57BL/6N-Tst<tm1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767836	F	MP:0005013	increased lymphocyte cell number	Tst<tm1(KOMP)Vlcg>/Tst<tm1(KOMP)Vlcg>	C57BL/6N-Tst<tm1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767836	M	MP:0001146	abnormal testis morphology	Tst<tm1(KOMP)Vlcg>/Tst<tm1(KOMP)Vlcg>	C57BL/6N-Tst<tm1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767836	M	MP:0002631	abnormal epididymis morphology	Tst<tm1(KOMP)Vlcg>/Tst<tm1(KOMP)Vlcg>	C57BL/6N-Tst<tm1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767836	M	MP:0001147	small testis	Tst<tm1(KOMP)Vlcg>/Tst<tm1(KOMP)Vlcg>	C57BL/6N-Tst<tm1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767836	M	MP:0004931	enlarged epididymis	Tst<tm1(KOMP)Vlcg>/Tst<tm1(KOMP)Vlcg>	C57BL/6N-Tst<tm1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767837	M	MP:0001146	abnormal testis morphology	Txndc5<tm1.1(KOMP)Vlcg>/Txndc5<tm1.1(KOMP)Vlcg>	C57BL/6N-Txndc5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767837	F	MP:0001399	hyperactivity	Txndc5<tm1.1(KOMP)Vlcg>/Txndc5<tm1.1(KOMP)Vlcg>	C57BL/6N-Txndc5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767837	M	MP:0002079	increased circulating insulin level	Txndc5<tm1.1(KOMP)Vlcg>/Txndc5<tm1.1(KOMP)Vlcg>	C57BL/6N-Txndc5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767837	M	MP:0001147	small testis	Txndc5<tm1.1(KOMP)Vlcg>/Txndc5<tm1.1(KOMP)Vlcg>	C57BL/6N-Txndc5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5767838	F	MP:0001399	hyperactivity	Ube2c<tm1.1(KOMP)Wtsi>/Ube2c<+>	C57BL/6N-Ube2c<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5767838	F	MP:0003984	embryonic growth retardation	Ube2c<tm1.1(KOMP)Wtsi>/Ube2c<+>	C57BL/6N-Ube2c<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5767840	F	MP:0010506	prolonged RR interval	Unc45a<tm1b(EUCOMM)Hmgu>/Unc45a<+>	C57BL/6N-Unc45a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5767840	M	MP:0001417	decreased exploration in new environment	Unc45a<tm1b(EUCOMM)Hmgu>/Unc45a<+>	C57BL/6N-Unc45a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5767840	F	MP:0005333	decreased heart rate	Unc45a<tm1b(EUCOMM)Hmgu>/Unc45a<+>	C57BL/6N-Unc45a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5767844	M	MP:0000208	decreased hematocrit	Wdr59<tm1b(EUCOMM)Wtsi>/Wdr59<+>	C57BL/6N-Wdr59<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767844	M	MP:0002874	decreased hemoglobin content	Wdr59<tm1b(EUCOMM)Wtsi>/Wdr59<+>	C57BL/6N-Wdr59<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767844	M	MP:0002875	decreased erythrocyte cell number	Wdr59<tm1b(EUCOMM)Wtsi>/Wdr59<+>	C57BL/6N-Wdr59<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767851	F	MP:0000063	decreased bone mineral density	Zfp260<tm1b(NCOM)Mfgc>/Zfp260<+>	C57BL/6N-Zfp260<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5767851	F	MP:0002764	short tibia	Zfp260<tm1b(NCOM)Mfgc>/Zfp260<+>	C57BL/6N-Zfp260<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5767852	M	MP:0001785	edema	Zfp260<tm1b(NCOM)Mfgc>/Zfp260<tm1b(NCOM)Mfgc>	C57BL/6N-Zfp260<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5767852	F	MP:0011100	preweaning lethality, complete penetrance	Zfp260<tm1b(NCOM)Mfgc>/Zfp260<tm1b(NCOM)Mfgc>	C57BL/6N-Zfp260<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5767853	F	MP:0002968	increased circulating alkaline phosphatase level	Zfp266<tm1b(EUCOMM)Wtsi>/Zfp266<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp266<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5767854	M	MP:0010097	abnormal retina blood vessel morphology	Zfp459<tm1b(EUCOMM)Wtsi>/Zfp459<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp459<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5767855	M	MP:0000745	tremors	Zfp60<tm1b(KOMP)Mbp>/Zfp60<tm1b(KOMP)Mbp>	C57BL/6N-Zfp60<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5767855	M	MP:0020870	decreased thigmotaxis	Zfp60<tm1b(KOMP)Mbp>/Zfp60<tm1b(KOMP)Mbp>	C57BL/6N-Zfp60<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5767855	M	MP:0004924	abnormal behavior	Zfp60<tm1b(KOMP)Mbp>/Zfp60<tm1b(KOMP)Mbp>	C57BL/6N-Zfp60<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5767856	M	MP:0001711	abnormal placenta morphology	Zwilch<tm1.1(KOMP)Vlcg>/Zwilch<tm1.1(KOMP)Vlcg>	C57BL/6N-Zwilch<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5769976	M	MP:0001147	small testis	Mad2l2<tm1.1Mpz>/Mad2l2<tm1.1Mpz>	involves: 129S2/SvPas * BALB/cJ	N	24009519
MGI:5769976	F	MP:0001126	abnormal ovary morphology	Mad2l2<tm1.1Mpz>/Mad2l2<tm1.1Mpz>	involves: 129S2/SvPas * BALB/cJ	N	24009519
MGI:5769976	F	MP:0001926	female infertility	Mad2l2<tm1.1Mpz>/Mad2l2<tm1.1Mpz>	involves: 129S2/SvPas * BALB/cJ	N	24009519
MGI:5769976	F	MP:0002777	absent ovarian follicles	Mad2l2<tm1.1Mpz>/Mad2l2<tm1.1Mpz>	involves: 129S2/SvPas * BALB/cJ	N	24009519
MGI:5769976	M	MP:0001152	increased Leydig cell number	Mad2l2<tm1.1Mpz>/Mad2l2<tm1.1Mpz>	involves: 129S2/SvPas * BALB/cJ	N	24009519
MGI:5769976	M	MP:0002216	abnormal seminiferous tubule morphology	Mad2l2<tm1.1Mpz>/Mad2l2<tm1.1Mpz>	involves: 129S2/SvPas * BALB/cJ	N	24009519
MGI:5769976	M	MP:0002784	abnormal Sertoli cell morphology	Mad2l2<tm1.1Mpz>/Mad2l2<tm1.1Mpz>	involves: 129S2/SvPas * BALB/cJ	N	24009519
MGI:5769976	M	MP:0001925	male infertility	Mad2l2<tm1.1Mpz>/Mad2l2<tm1.1Mpz>	involves: 129S2/SvPas * BALB/cJ	N	24009519
MGI:5769976	M	MP:0006428	ectopic Sertoli cells	Mad2l2<tm1.1Mpz>/Mad2l2<tm1.1Mpz>	involves: 129S2/SvPas * BALB/cJ	N	24009519
MGI:5769976	F	MP:0001127	small ovary	Mad2l2<tm1.1Mpz>/Mad2l2<tm1.1Mpz>	involves: 129S2/SvPas * BALB/cJ	N	24009519
MGI:5769976	F	MP:0003578	absent ovary	Mad2l2<tm1.1Mpz>/Mad2l2<tm1.1Mpz>	involves: 129S2/SvPas * BALB/cJ	N	24009519
MGI:5769990	M	MP:0005159	azoospermia	Rbm5<sda>/Rbm5<sda>	involves: C57BL/6J * CBA	N	23935508
MGI:5769990	M	MP:0003205	testicular atrophy	Rbm5<sda>/Rbm5<sda>	involves: C57BL/6J * CBA	N	23935508
MGI:5769990	M	MP:0008279	arrest of spermiogenesis	Rbm5<sda>/Rbm5<sda>	involves: C57BL/6J * CBA	N	23935508
MGI:5769990	M	MP:0004852	decreased testis weight	Rbm5<sda>/Rbm5<sda>	involves: C57BL/6J * CBA	N	23935508
MGI:5769990	M	MP:0001155	arrest of spermatogenesis	Rbm5<sda>/Rbm5<sda>	involves: C57BL/6J * CBA	N	23935508
MGI:5769990	M	MP:0014052	increased male germ cell apoptosis	Rbm5<sda>/Rbm5<sda>	involves: C57BL/6J * CBA	N	23935508
MGI:5769990	M	MP:0001925	male infertility	Rbm5<sda>/Rbm5<sda>	involves: C57BL/6J * CBA	N	23935508
MGI:5770122	M	MP:0005480	increased circulating triiodothyronine level	Dio3<tm1Dmst>/Dio3<tm1Dmst>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * DBA	N	25004090
MGI:5770122	M	MP:0005477	increased circulating thyroxine level	Dio3<tm1Dmst>/Dio3<tm1Dmst>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * DBA	N	25004090
MGI:5770122	M	MP:0005164	abnormal response to injury	Dio3<tm1Dmst>/Dio3<tm1Dmst>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * DBA	N	25004090
MGI:5770122	M	MP:0005376	homeostasis/metabolism phenotype	Dio3<tm1Dmst>/Dio3<tm1Dmst>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * DBA	Y	25004090
MGI:5770122	M	MP:0003893	increased hepatocyte proliferation	Dio3<tm1Dmst>/Dio3<tm1Dmst>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * DBA	N	25004090
MGI:5770122	M	MP:0005378	growth/size/body region phenotype	Dio3<tm1Dmst>/Dio3<tm1Dmst>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * DBA	Y	25004090
MGI:5770122	M	MP:0005370	liver/biliary system phenotype	Dio3<tm1Dmst>/Dio3<tm1Dmst>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * DBA	Y	25004090
MGI:5770244	M	MP:0001529	abnormal vocalization	Brinp1<tm1.1Pib>/Brinp1<tm1.1Pib>	involves: BALB/cJ * C57BL/6	N	27042284
MGI:5770244	F	MP:0001442	decreased grooming behavior	Brinp1<tm1.1Pib>/Brinp1<tm1.1Pib>	involves: BALB/cJ * C57BL/6	N	27042284
MGI:5770244	M	MP:0013189	abnormal exploration in a new environment	Brinp1<tm1.1Pib>/Brinp1<tm1.1Pib>	involves: BALB/cJ * C57BL/6	N	27042284
MGI:5770257	F	MP:0008489	slow postnatal weight gain	Brinp1<tm1.1Pib>/Brinp1<+>	involves: BALB/cJ * C57BL/6	N	27042284
MGI:5770257	M	MP:0001262	decreased body weight	Brinp1<tm1.1Pib>/Brinp1<+>	involves: BALB/cJ * C57BL/6	N	27042284
MGI:5770262	M	MP:0003631	nervous system phenotype	Gys1<tm1c(EUCOMM)Wtsi>/Gys1<tm1c(EUCOMM)Wtsi>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL	Y	23281428
MGI:5770262	M	MP:0014075	decreased brain glycogen level	Gys1<tm1c(EUCOMM)Wtsi>/Gys1<tm1c(EUCOMM)Wtsi>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	23281428
MGI:5770262	M	MP:0001900	impaired synaptic plasticity	Gys1<tm1c(EUCOMM)Wtsi>/Gys1<tm1c(EUCOMM)Wtsi>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	23281428
MGI:5770262	M	MP:0001473	reduced long-term potentiation	Gys1<tm1c(EUCOMM)Wtsi>/Gys1<tm1c(EUCOMM)Wtsi>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	23281428
MGI:5770262	M	MP:0002919	enhanced paired-pulse facilitation	Gys1<tm1c(EUCOMM)Wtsi>/Gys1<tm1c(EUCOMM)Wtsi>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	23281428
MGI:5770262	M	MP:0002803	abnormal operant conditioning behavior	Gys1<tm1c(EUCOMM)Wtsi>/Gys1<tm1c(EUCOMM)Wtsi>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	23281428
MGI:5770444	M	MP:0004182	abnormal spermiation	Tmem203<tm1.1Roml>/Tmem203<tm1.1Roml>	involves: C57BL/6	N	25996873
MGI:5770444	M	MP:0001925	male infertility	Tmem203<tm1.1Roml>/Tmem203<tm1.1Roml>	involves: C57BL/6	N	25996873
MGI:5770444	M	MP:0009230	abnormal sperm head morphology	Tmem203<tm1.1Roml>/Tmem203<tm1.1Roml>	involves: C57BL/6	N	25996873
MGI:5770444	M	MP:0005389	reproductive system phenotype	Tmem203<tm1.1Roml>/Tmem203<tm1.1Roml>	involves: C57BL/6	Y	25996873
MGI:5770444	M	MP:0001146	abnormal testis morphology	Tmem203<tm1.1Roml>/Tmem203<tm1.1Roml>	involves: C57BL/6	N	25996873
MGI:5770444	M	MP:0004852	decreased testis weight	Tmem203<tm1.1Roml>/Tmem203<tm1.1Roml>	involves: C57BL/6	N	25996873
MGI:5770444	M	MP:0001154	seminiferous tubule degeneration	Tmem203<tm1.1Roml>/Tmem203<tm1.1Roml>	involves: C57BL/6	N	25996873
MGI:5770444	F	MP:0001923	reduced female fertility	Tmem203<tm1.1Roml>/Tmem203<tm1.1Roml>	involves: C57BL/6	N	25996873
MGI:5770444	M	MP:0005159	azoospermia	Tmem203<tm1.1Roml>/Tmem203<tm1.1Roml>	involves: C57BL/6	N	25996873
MGI:5770635	F	MP:0011384	abnormal progesterone level	Hsd17b1<tm1(KOMP)Vlcg>/Hsd17b1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26018678
MGI:5770635	F	MP:0002636	delayed vaginal opening	Hsd17b1<tm1(KOMP)Vlcg>/Hsd17b1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26018678
MGI:5770635	F	MP:0001923	reduced female fertility	Hsd17b1<tm1(KOMP)Vlcg>/Hsd17b1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26018678
MGI:5770635	F	MP:0002680	decreased corpora lutea number	Hsd17b1<tm1(KOMP)Vlcg>/Hsd17b1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26018678
MGI:5770635	F	MP:0004855	increased ovary weight	Hsd17b1<tm1(KOMP)Vlcg>/Hsd17b1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26018678
MGI:5770635	F	MP:0001126	abnormal ovary morphology	Hsd17b1<tm1(KOMP)Vlcg>/Hsd17b1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26018678
MGI:5770635	F	MP:0005389	reproductive system phenotype	Hsd17b1<tm1(KOMP)Vlcg>/Hsd17b1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	Y	26018678
MGI:5770635	F	MP:0002679	abnormal corpus luteum morphology	Hsd17b1<tm1(KOMP)Vlcg>/Hsd17b1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26018678
MGI:5770635	F	MP:0004903	abnormal uterus weight	Hsd17b1<tm1(KOMP)Vlcg>/Hsd17b1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26018678
MGI:5770635	F	MP:0001935	decreased litter size	Hsd17b1<tm1(KOMP)Vlcg>/Hsd17b1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26018678
MGI:5770635	F	MP:0005133	increased luteinizing hormone level	Hsd17b1<tm1(KOMP)Vlcg>/Hsd17b1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26018678
MGI:5770649	F	MP:0001402	decreased locomotor activity	Ciz1<Gt(IST13830B6)Tigm>/Ciz1<Gt(IST13830B6)Tigm>	B6J.B6N-Ciz1<Gt(IST13830B6)Tigm>	N	27163549
MGI:5770649	M	MP:0001399	hyperactivity	Ciz1<Gt(IST13830B6)Tigm>/Ciz1<Gt(IST13830B6)Tigm>	B6J.B6N-Ciz1<Gt(IST13830B6)Tigm>	N	27163549
MGI:5770649	F	MP:0001405	impaired coordination	Ciz1<Gt(IST13830B6)Tigm>/Ciz1<Gt(IST13830B6)Tigm>	B6J.B6N-Ciz1<Gt(IST13830B6)Tigm>	N	27163549
MGI:5770649	M	MP:0001353	increased aggression towards mice	Ciz1<Gt(IST13830B6)Tigm>/Ciz1<Gt(IST13830B6)Tigm>	B6J.B6N-Ciz1<Gt(IST13830B6)Tigm>	N	27163549
MGI:5770649	F	MP:0001407	short stride length	Ciz1<Gt(IST13830B6)Tigm>/Ciz1<Gt(IST13830B6)Tigm>	B6J.B6N-Ciz1<Gt(IST13830B6)Tigm>	N	27163549
MGI:5770657	M	MP:0000165	abnormal long bone hypertrophic chondrocyte zone	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0001262	decreased body weight	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0009346	decreased trabecular bone thickness	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0003109	short femur	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0014105	abnormal chondrocyte differentiation	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0014101	decreased chondrocyte proliferation	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0010869	decreased bone trabecula number	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0001258	decreased body length	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0001265	decreased body size	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0010879	decreased trabecular bone volume	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0001255	decreased body height	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0013616	decreased volumetric bone mineral density	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0008271	abnormal bone ossification	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0000135	decreased compact bone thickness	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0008272	abnormal endochondral bone ossification	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0003662	abnormal long bone epiphyseal plate proliferative zone	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0002764	short tibia	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0004989	decreased osteoblast cell number	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0002113	abnormal skeleton development	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770657	M	MP:0000130	abnormal trabecular bone morphology	Scube2<tm1.1Rbya>/Scube2<tm1.1Rbya>	B6.129-Scube2<tm1.1Rbya>	N	25639508
MGI:5770783	M	MP:0008898	abnormal acrosome morphology	Best1<tm1Web>/Best1<tm1Web>	B6.129S1-Best1<tm1Web>	N	25941382
MGI:5770783	M	MP:0008892	abnormal sperm flagellum morphology	Best1<tm1Web>/Best1<tm1Web>	B6.129S1-Best1<tm1Web>	N	25941382
MGI:5770783	M	MP:0001922	reduced male fertility	Best1<tm1Web>/Best1<tm1Web>	B6.129S1-Best1<tm1Web>	N	25941382
MGI:5770783	M	MP:0001935	decreased litter size	Best1<tm1Web>/Best1<tm1Web>	B6.129S1-Best1<tm1Web>	N	25941382
MGI:5770786	M	MP:0004543	abnormal sperm physiology	Best1<tm1Web>/Best1<tm1Web>	involves: CD-1	N	25941382
MGI:5770786	M	MP:0001922	reduced male fertility	Best1<tm1Web>/Best1<tm1Web>	involves: CD-1	N	25941382
MGI:5770786	M	MP:0008898	abnormal acrosome morphology	Best1<tm1Web>/Best1<tm1Web>	involves: CD-1	N	25941382
MGI:5770786	M	MP:0002675	asthenozoospermia	Best1<tm1Web>/Best1<tm1Web>	involves: CD-1	N	25941382
MGI:5770786	M	MP:0008839	absent acrosome	Best1<tm1Web>/Best1<tm1Web>	involves: CD-1	N	25941382
MGI:5770786	M	MP:0009325	necrospermia	Best1<tm1Web>/Best1<tm1Web>	involves: CD-1	N	25941382
MGI:5770786	M	MP:0008893	detached sperm flagellum	Best1<tm1Web>/Best1<tm1Web>	involves: CD-1	N	25941382
MGI:5770786	M	MP:0009237	kinked sperm flagellum	Best1<tm1Web>/Best1<tm1Web>	involves: CD-1	N	25941382
MGI:5770786	M	MP:0009238	coiled sperm flagellum	Best1<tm1Web>/Best1<tm1Web>	involves: CD-1	N	25941382
MGI:5771573	M	MP:0030935	increased primordial germ cell apoptosis	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26490168
MGI:5771573	F	MP:0003582	abnormal ovary development	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26637282
MGI:5771573	M	MP:0010948	abnormal double-strand DNA break repair	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26490168
MGI:5771573	M	MP:0004852	decreased testis weight	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26490168
MGI:5771573	M	MP:0004852	decreased testis weight	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26637282
MGI:5771573	F	MP:0011125	decreased primary ovarian follicle number	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26637282
MGI:5771573	M	MP:0003205	testicular atrophy	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26637282
MGI:5771573	M	MP:0013538	increased Harderian gland adenoma incidence	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26637282
MGI:5771573	M	MP:0002776	increased Sertoli cell number	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26637282
MGI:5771573	F	MP:0002041	increased pituitary adenoma incidence	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26637282
MGI:5771573	F	MP:0002016	ovary cyst	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26637282
MGI:5771573	F	MP:0009092	endometrium hyperplasia	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26637282
MGI:5771573	M	MP:0002687	oligozoospermia	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26490168
MGI:5771573	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26490168
MGI:5771573	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26490168
MGI:5771573	M	MP:0006378	abnormal spermatogonia morphology	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26637282
MGI:5771573	M	MP:0002216	abnormal seminiferous tubule morphology	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26637282
MGI:5771573	M	MP:0008966	abnormal chiasmata formation	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26490168
MGI:5771573	M	MP:0002685	abnormal spermatogonia proliferation	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26490168
MGI:5771573	M	MP:0001147	small testis	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26490168
MGI:5771573	M	MP:0001147	small testis	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26637282
MGI:5771573	M	MP:0030934	decreased primordial germ cell proliferation	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26490168
MGI:5771573	M	MP:0008392	decreased primordial germ cell number	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26490168
MGI:5771573	M	MP:0001940	testis hypoplasia	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>	involves: 129P2/OlaHsd	N	26490168
MGI:5771655	M	MP:0002216	abnormal seminiferous tubule morphology	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>,Fancd2<tm1Hou>/Fancd2<tm1Hou>	involves: 129P2/OlaHsd * 129S4/SvJae	N	26637282
MGI:5771655	M	MP:0001147	small testis	Brip1<Gt(RRI409)Byg>/Brip1<Gt(RRI409)Byg>,Fancd2<tm1Hou>/Fancd2<tm1Hou>	involves: 129P2/OlaHsd * 129S4/SvJae	N	26637282
MGI:5771865	M	MP:0006116	calcified aortic valve	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0002747	abnormal aortic valve morphology	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0012688	abnormal heart ventricles weight	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0002079	increased circulating insulin level	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0005140	decreased cardiac muscle contractility	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0011951	increased cardiac stroke volume	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0011572	abnormal aorta bulb morphology	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0003394	increased cardiac output	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0010139	aortitis	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0001544	abnormal cardiovascular system physiology	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0001625	cardiac hypertrophy	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0003921	abnormal heart left ventricle morphology	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0002625	heart left ventricle hypertrophy	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0003141	cardiac fibrosis	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0013277	abnormal fasting circulating glucose level	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0005178	increased circulating cholesterol level	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771865	M	MP:0006117	aortic valve stenosis	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>,Tg(Ins-Igf2)1Fbos/?	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	N	25231636
MGI:5771869	M	MP:0005140	decreased cardiac muscle contractility	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>	involves: 129S7/SvEvBrd * C57BL/6J	N	25231636
MGI:5771869	M	MP:0005178	increased circulating cholesterol level	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>	involves: 129S7/SvEvBrd * C57BL/6J	N	25231636
MGI:5771869	M	MP:0011951	increased cardiac stroke volume	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>	involves: 129S7/SvEvBrd * C57BL/6J	N	25231636
MGI:5771869	M	MP:0011572	abnormal aorta bulb morphology	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>	involves: 129S7/SvEvBrd * C57BL/6J	N	25231636
MGI:5771869	M	MP:0002079	increased circulating insulin level	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>	involves: 129S7/SvEvBrd * C57BL/6J	N	25231636
MGI:5771869	M	MP:0006117	aortic valve stenosis	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>	involves: 129S7/SvEvBrd * C57BL/6J	N	25231636
MGI:5771869	M	MP:0003394	increased cardiac output	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>	involves: 129S7/SvEvBrd * C57BL/6J	N	25231636
MGI:5771869	M	MP:0012688	abnormal heart ventricles weight	Apob<tm2Sgy>/Apob<tm2Sgy>,Ldlr<tm1Her>/Ldlr<tm1Her>	involves: 129S7/SvEvBrd * C57BL/6J	N	25231636
MGI:5771995	F	MP:0013279	increased fasting circulating glucose level	Ccdc120<tm1.1(KOMP)Vlcg>/Ccdc120<tm1.1(KOMP)Vlcg>	B6N(Cg)-Ccdc120<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5771995	F	MP:0001399	hyperactivity	Ccdc120<tm1.1(KOMP)Vlcg>/Ccdc120<tm1.1(KOMP)Vlcg>	B6N(Cg)-Ccdc120<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5774702	M	MP:0009936	abnormal dendritic spine morphology	Cyfip2<tm1(KOMP)Vlcg>/Cyfip2<+>	involves: C57BL/6J * C57BL/6NTac	N	25432536
MGI:5774702	M	MP:0001489	decreased startle reflex	Cyfip2<tm1(KOMP)Vlcg>/Cyfip2<+>	involves: C57BL/6J * C57BL/6NTac	N	25432536
MGI:5774702	M	MP:0001399	hyperactivity	Cyfip2<tm1(KOMP)Vlcg>/Cyfip2<+>	involves: C57BL/6J * C57BL/6NTac	N	25432536
MGI:5774702	M	MP:0003631	nervous system phenotype	Cyfip2<tm1(KOMP)Vlcg>/Cyfip2<+>	involves: C57BL/6J * C57BL/6NTac	Y	25432536
MGI:5774702	M	MP:0009141	increased prepulse inhibition	Cyfip2<tm1(KOMP)Vlcg>/Cyfip2<+>	involves: C57BL/6J * C57BL/6NTac	N	25432536
MGI:5774702	M	MP:0001362	abnormal anxiety-related response	Cyfip2<tm1(KOMP)Vlcg>/Cyfip2<+>	involves: C57BL/6J * C57BL/6NTac	N	25432536
MGI:5774703	M	MP:0001489	decreased startle reflex	Cyfip2<tm1(KOMP)Vlcg>/Cyfip2<+>,Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac	N	25432536
MGI:5774703	M	MP:0009141	increased prepulse inhibition	Cyfip2<tm1(KOMP)Vlcg>/Cyfip2<+>,Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac	N	25432536
MGI:5774703	M	MP:0009936	abnormal dendritic spine morphology	Cyfip2<tm1(KOMP)Vlcg>/Cyfip2<+>,Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac	N	25432536
MGI:5774703	M	MP:0001399	hyperactivity	Cyfip2<tm1(KOMP)Vlcg>/Cyfip2<+>,Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac	N	25432536
MGI:5774703	M	MP:0001409	increased stereotypic behavior	Cyfip2<tm1(KOMP)Vlcg>/Cyfip2<+>,Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac	N	25432536
MGI:5774703	M	MP:0001362	abnormal anxiety-related response	Cyfip2<tm1(KOMP)Vlcg>/Cyfip2<+>,Fmr1<tm1Cgr>/Y	involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac	N	25432536
MGI:5774970	M	MP:0003984	embryonic growth retardation	Ddx3x<tm1.2Lyou>/Y	involves: 129 * C57BL/6	N	27179789
MGI:5774970	M	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance	Ddx3x<tm1.2Lyou>/Y	involves: 129 * C57BL/6	N	27179789
MGI:5774970	M	MP:0011105	embryonic lethality between implantation and placentation, incomplete penetrance	Ddx3x<tm1.2Lyou>/Y	involves: 129 * C57BL/6	N	27179789
MGI:5774970	M	MP:0001713	decreased trophoblast giant cell number	Ddx3x<tm1.2Lyou>/Y	involves: 129 * C57BL/6	N	27179789
MGI:5774971	F	MP:0008803	abnormal placental labyrinth vasculature morphology	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	N	27179789
MGI:5774971	F	MP:0001713	decreased trophoblast giant cell number	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	N	27179789
MGI:5774971	F	MP:0010768	mortality/aging	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	Y	27179789
MGI:5774971	F	MP:0012099	decreased spongiotrophoblast size	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	N	27179789
MGI:5774971	F	MP:0003231	abnormal placenta vasculature	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	N	27179789
MGI:5774971	F	MP:0004259	small placenta	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	N	27179789
MGI:5774971	F	MP:0001914	hemorrhage	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	N	27179789
MGI:5774971	F	MP:0001785	edema	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	N	27179789
MGI:5774971	F	MP:0011100	preweaning lethality, complete penetrance	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	N	27179789
MGI:5774971	F	MP:0005033	abnormal trophoblast giant cell morphology	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	N	27179789
MGI:5774971	F	MP:0030989	decreased spongiotrophoblast cell number	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	N	27179789
MGI:5774971	F	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	N	27179789
MGI:5774971	F	MP:0010402	ventricular septal defect	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	N	27179789
MGI:5774971	F	MP:0003984	embryonic growth retardation	Ddx3x<tm1.2Lyou>/Ddx3x<+>	involves: 129 * C57BL/6	N	27179789
MGI:5774972	M	MP:0000433	microcephaly	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0004559	small allantois	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0005312	pericardial effusion	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0011100	preweaning lethality, complete penetrance	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0004760	increased mitotic index	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0001700	abnormal embryo turning	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0001726	abnormal allantois morphology	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0002084	abnormal developmental patterning	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0011257	abnormal head fold morphology	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0003077	abnormal cell cycle	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0002189	abnormal myocardial trabeculae morphology	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0000913	abnormal brain development	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0003984	embryonic growth retardation	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0003720	abnormal neural tube closure	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0009657	failure of chorioallantoic fusion	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0005621	abnormal cell physiology	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0013504	increased embryonic tissue cell apoptosis	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774972	M	MP:0013293	embryonic lethality prior to tooth bud stage	Ddx3x<tm1.1Lyou>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5774973	F	MP:0002169	no abnormal phenotype detected	Ddx3x<tm1.1Lyou>/Ddx3x<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129 * C57BL/6 * CBA	N	27179789
MGI:5775111	F	MP:0003631	nervous system phenotype	Pgrmc1<tm1.1Jjp>/Pgrmc1<tm1.1Jjp>,Omp<tm1(cre)Jae>/Omp<+>	involves: 129S1/Sv	Y	26046438
MGI:5775111	F	MP:0005394	taste/olfaction phenotype	Pgrmc1<tm1.1Jjp>/Pgrmc1<tm1.1Jjp>,Omp<tm1(cre)Jae>/Omp<+>	involves: 129S1/Sv	Y	26046438
MGI:5775111	F	MP:0002067	abnormal sensory capabilities/reflexes/nociception	Pgrmc1<tm1.1Jjp>/Pgrmc1<tm1.1Jjp>,Omp<tm1(cre)Jae>/Omp<+>	involves: 129S1/Sv	N	26046438
MGI:5775112	F	MP:0011678	abnormal vomeronasal sensory neuron physiology	Plcb2<tm1Dwu>/Plcb2<tm1Dwu>	B6.129S1-Plcb2<tm1Dwu>/J	N	26046438
MGI:5775112	F	MP:0002067	abnormal sensory capabilities/reflexes/nociception	Plcb2<tm1Dwu>/Plcb2<tm1Dwu>	B6.129S1-Plcb2<tm1Dwu>/J	N	26046438
MGI:5775134	M	MP:0031633	decreased heart left ventricle muscle contractility	Akap13<Gt(CSJ306)Byg>/Akap13<Gt(CSJ306)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23658642
MGI:5775134	M	MP:0005608	cardiac interstitial fibrosis	Akap13<Gt(CSJ306)Byg>/Akap13<Gt(CSJ306)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23658642
MGI:5775134	M	MP:0004484	abnormal response of heart to induced stress	Akap13<Gt(CSJ306)Byg>/Akap13<Gt(CSJ306)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23658642
MGI:5775429	F	MP:0009083	uterus hypertrophy	Cdh5<tm1.1Ics>/Cdh5<tm1.1Ics>	B6.129(Cg)-Cdh5<tm1.1Ics>	N	24858856
MGI:5775429	F	MP:0013607	ovary fibrosis	Cdh5<tm1.1Ics>/Cdh5<tm1.1Ics>	B6.129(Cg)-Cdh5<tm1.1Ics>	N	24858856
MGI:5775429	F	MP:0013398	uterus fibrosis	Cdh5<tm1.1Ics>/Cdh5<tm1.1Ics>	B6.129(Cg)-Cdh5<tm1.1Ics>	N	24858856
MGI:5775429	F	MP:0004832	enlarged ovary	Cdh5<tm1.1Ics>/Cdh5<tm1.1Ics>	B6.129(Cg)-Cdh5<tm1.1Ics>	N	24858856
MGI:5775429	F	MP:0004906	enlarged uterus	Cdh5<tm1.1Ics>/Cdh5<tm1.1Ics>	B6.129(Cg)-Cdh5<tm1.1Ics>	N	24858856
MGI:5775429	F	MP:0009444	ovarian follicular cyst	Cdh5<tm1.1Ics>/Cdh5<tm1.1Ics>	B6.129(Cg)-Cdh5<tm1.1Ics>	N	24858856
MGI:5775429	F	MP:0001126	abnormal ovary morphology	Cdh5<tm1.1Ics>/Cdh5<tm1.1Ics>	B6.129(Cg)-Cdh5<tm1.1Ics>	N	24858856
MGI:5775429	F	MP:0001120	abnormal uterus morphology	Cdh5<tm1.1Ics>/Cdh5<tm1.1Ics>	B6.129(Cg)-Cdh5<tm1.1Ics>	N	24858856
MGI:5775429	F	MP:0009251	enlarged endometrial glands	Cdh5<tm1.1Ics>/Cdh5<tm1.1Ics>	B6.129(Cg)-Cdh5<tm1.1Ics>	N	24858856
MGI:5775429	F	MP:0001785	edema	Cdh5<tm1.1Ics>/Cdh5<tm1.1Ics>	B6.129(Cg)-Cdh5<tm1.1Ics>	N	24858856
MGI:5775429	F	MP:0006055	abnormal vascular endothelial cell morphology	Cdh5<tm1.1Ics>/Cdh5<tm1.1Ics>	B6.129(Cg)-Cdh5<tm1.1Ics>	N	24858856
MGI:5775429	F	MP:0002016	ovary cyst	Cdh5<tm1.1Ics>/Cdh5<tm1.1Ics>	B6.129(Cg)-Cdh5<tm1.1Ics>	N	24858856
MGI:5775603	F	MP:0001272	increased metastatic potential	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-ERBB2)#Jjz/0	involves: FVB/N	N	26977878
MGI:5775603	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-ERBB2)#Jjz/0	involves: FVB/N	N	26977878
MGI:5775603	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-ERBB2)#Jjz/0	involves: FVB/N	N	26977878
MGI:5776509	M	MP:0014367	impaired long-term object recognition memory	Sorbs2<tm1.2Gfng>/Sorbs2<tm1.2Gfng>	B6.129(FVB)-Sorbs2<tm1.2Gfng>	N	26888934
MGI:5776509	M	MP:0005386	behavior/neurological phenotype	Sorbs2<tm1.2Gfng>/Sorbs2<tm1.2Gfng>	B6.129(FVB)-Sorbs2<tm1.2Gfng>	Y	26888934
MGI:5776509	M	MP:0009454	impaired contextual conditioning behavior	Sorbs2<tm1.2Gfng>/Sorbs2<tm1.2Gfng>	B6.129(FVB)-Sorbs2<tm1.2Gfng>	N	26888934
MGI:5776509	M	MP:0009142	decreased prepulse inhibition	Sorbs2<tm1.2Gfng>/Sorbs2<tm1.2Gfng>	B6.129(FVB)-Sorbs2<tm1.2Gfng>	N	26888934
MGI:5776509	M	MP:0001489	decreased startle reflex	Sorbs2<tm1.2Gfng>/Sorbs2<tm1.2Gfng>	B6.129(FVB)-Sorbs2<tm1.2Gfng>	N	26888934
MGI:5779409	M	MP:0003186	abnormal redox activity	Cyba<tm1Dgh>/Cyba<tm1Dgh>	B6.Cg-Cyba<tm1Dgh>	N	23248154
MGI:5779409	M	MP:0005333	decreased heart rate	Cyba<tm1Dgh>/Cyba<tm1Dgh>	B6.Cg-Cyba<tm1Dgh>	N	23248154
MGI:5779409	M	MP:0003633	abnormal nervous system physiology	Cyba<tm1Dgh>/Cyba<tm1Dgh>	B6.Cg-Cyba<tm1Dgh>	N	23248154
MGI:5779409	M	MP:0004183	abnormal sympathetic nervous system physiology	Cyba<tm1Dgh>/Cyba<tm1Dgh>	B6.Cg-Cyba<tm1Dgh>	N	23248154
MGI:5779409	M	MP:0001876	decreased inflammatory response	Cyba<tm1Dgh>/Cyba<tm1Dgh>	B6.Cg-Cyba<tm1Dgh>	N	23248154
MGI:5779409	M	MP:0001828	abnormal T cell activation	Cyba<tm1Dgh>/Cyba<tm1Dgh>	B6.Cg-Cyba<tm1Dgh>	N	23248154
MGI:5779409	M	MP:0004876	decreased mean systemic arterial blood pressure	Cyba<tm1Dgh>/Cyba<tm1Dgh>	B6.Cg-Cyba<tm1Dgh>	N	23248154
MGI:5779409	M	MP:0010697	abnormal systemic arterial blood pressure regulation	Cyba<tm1Dgh>/Cyba<tm1Dgh>	B6.Cg-Cyba<tm1Dgh>	N	23248154
MGI:5779409	M	MP:0003929	decreased heart rate variability	Cyba<tm1Dgh>/Cyba<tm1Dgh>	B6.Cg-Cyba<tm1Dgh>	N	23248154
MGI:5779409	M	MP:0000230	abnormal systemic arterial blood pressure	Cyba<tm1Dgh>/Cyba<tm1Dgh>	B6.Cg-Cyba<tm1Dgh>	N	23248154
MGI:5779417	F	MP:0001923	reduced female fertility	Tg(Pmp22)My41Clh/0	involves: C57BL/6J * CBA/Ca	N	12090404
MGI:5779417	M	MP:0001925	male infertility	Tg(Pmp22)My41Clh/0	involves: C57BL/6J * CBA/Ca	N	12090404
MGI:5779540	M	MP:0001925	male infertility	Adcy10<tm1.2Geno>/Adcy10<tm1.2Geno>	involves: 129 * C57BL/6	N	23611875
MGI:5779541	F	MP:0003579	increased ovarian carcinoma incidence	Apc<tm1Tno>/Apc<tm1Tno>,Pten<tm2Mak>/Pten<tm2Mak>	involves: 129P2/OlaHsd * 129S4/SvJae	N	17418409
MGI:5779541	F	MP:0013184	hemorrhagic ascites	Apc<tm1Tno>/Apc<tm1Tno>,Pten<tm2Mak>/Pten<tm2Mak>	involves: 129P2/OlaHsd * 129S4/SvJae	N	17418409
MGI:5779541	F	MP:0014237	decreased tumor-free survival time	Apc<tm1Tno>/Apc<tm1Tno>,Pten<tm2Mak>/Pten<tm2Mak>	involves: 129P2/OlaHsd * 129S4/SvJae	N	17418409
MGI:5779542	M	MP:0001156	abnormal spermatogenesis	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * C57BL/6	N	25238791
MGI:5779542	M	MP:0003893	increased hepatocyte proliferation	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * C57BL/6	N	25238791
MGI:5779542	M	MP:0004852	decreased testis weight	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * C57BL/6	N	25238791
MGI:5779542	M	MP:0010897	abnormal bronchiole epithelium morphology	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * C57BL/6	N	25238791
MGI:5779542	M	MP:0001153	small seminiferous tubules	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * C57BL/6	N	25238791
MGI:5779542	M	MP:0002687	oligozoospermia	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * C57BL/6	N	25238791
MGI:5779542	M	MP:0005159	azoospermia	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * C57BL/6	N	25238791
MGI:5779542	M	MP:0001732	postnatal growth retardation	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * C57BL/6	N	25238791
MGI:5779542	M	MP:0005389	reproductive system phenotype	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * C57BL/6	Y	25238791
MGI:5779542	M	MP:0001262	decreased body weight	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * C57BL/6	N	25238791
MGI:5779542	M	MP:0010901	abnormal pulmonary alveolar parenchyma morphology	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	involves: 129S/SvEv * C57BL/6	N	25238791
MGI:5779552	M	MP:0001363	increased anxiety-related response	Tg(C9orf72*)450BLagi/?	involves: C3H * C57BL/6	N	27112497
MGI:5779928	M	MP:0001489	decreased startle reflex	Dixdc1<tm1Bnrc>/Dixdc1<tm1Bnrc>	involves: 129 * C57BL/6	N	22832659
MGI:5779928	M	MP:0001402	decreased locomotor activity	Dixdc1<tm1Bnrc>/Dixdc1<tm1Bnrc>	involves: 129 * C57BL/6	N	22832659
MGI:5779928	M	MP:0002757	decreased vertical activity	Dixdc1<tm1Bnrc>/Dixdc1<tm1Bnrc>	involves: 129 * C57BL/6	N	22832659
MGI:5779928	M	MP:0001363	increased anxiety-related response	Dixdc1<tm1Bnrc>/Dixdc1<tm1Bnrc>	involves: 129 * C57BL/6	N	22832659
MGI:5779928	M	MP:0003631	nervous system phenotype	Dixdc1<tm1Bnrc>/Dixdc1<tm1Bnrc>	involves: 129 * C57BL/6	Y	22832659
MGI:5779928	M	MP:0001406	abnormal gait	Dixdc1<tm1Bnrc>/Dixdc1<tm1Bnrc>	involves: 129 * C57BL/6	N	22832659
MGI:5779956	F	MP:0001732	postnatal growth retardation	Rack1<tm1Sbif>/Rack1<+>	C57BL/6-Rack1<tm1Sbif>	N	23212600
MGI:5779956	F	MP:0001258	decreased body length	Rack1<tm1Sbif>/Rack1<+>	C57BL/6-Rack1<tm1Sbif>	N	23212600
MGI:5779956	F	MP:0001262	decreased body weight	Rack1<tm1Sbif>/Rack1<+>	C57BL/6-Rack1<tm1Sbif>	N	23212600
MGI:5779963	M	MP:0002705	dilated renal tubule	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0030940	impaired autophagy	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0011351	absent proximal convoluted tubule brush border	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0002871	albuminuria	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0002962	increased urine protein level	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0011282	increased podocyte apoptosis	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0020378	abnormal cell cytoskeleton morphology	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0009640	abnormal renal tubule epithelium morphology	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0011402	renal cast	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0005565	increased blood urea nitrogen level	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0008140	podocyte foot process effacement	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0005419	decreased circulating serum albumin level	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0011085	postnatal lethality, complete penetrance	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0005326	abnormal podocyte morphology	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0005178	increased circulating cholesterol level	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779963	M	MP:0005553	increased circulating creatinine level	Atp6ap2<tm1.1Ics>/Y,Tg(NPHS2-cre)295Lbh/0	involves: C57BL/6 * C57BL/6N * SJL	N	22034640
MGI:5779964	M	MP:0030940	impaired autophagy	Atp6ap2<tm1.1Ics>/Y	involves: C57BL/6 * C57BL/6N	N	22034640
MGI:5779968	F	MP:0012185	abnormal muscle precursor cell morphology	Kdm6a<tm1.1Kaig>/Kdm6a<tm1.1Kaig>,Pax7<tm2.1(cre/ERT2)Fan>/Pax7<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	26999603
MGI:5779968	F	MP:0013239	impaired skeletal muscle regeneration	Kdm6a<tm1.1Kaig>/Kdm6a<tm1.1Kaig>,Pax7<tm2.1(cre/ERT2)Fan>/Pax7<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	26999603
MGI:5779969	M	MP:0013239	impaired skeletal muscle regeneration	Gt(ROSA)26Sor<tm4(ACTB-tdTomato,-EGFP)Luo>/Gt(ROSA)26Sor<+>,Kdm6a<tm1.1Kaig>/Y,Pax7<tm2.1(cre/ERT2)Fan>/Pax7<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	26999603
MGI:5779970	M	MP:0013239	impaired skeletal muscle regeneration	Kdm6a<tm1.1Kaig>/Y,Pax7<tm2.1(cre/ERT2)Fan>/Pax7<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	26999603
MGI:5779970	M	MP:0012185	abnormal muscle precursor cell morphology	Kdm6a<tm1.1Kaig>/Y,Pax7<tm2.1(cre/ERT2)Fan>/Pax7<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	26999603
MGI:5779971	M	MP:0013239	impaired skeletal muscle regeneration	Kdm6a<tm2.1Kaig>/Y	involves: 129 * C57BL/6	N	26999603
MGI:5779971	M	MP:0005369	muscle phenotype	Kdm6a<tm2.1Kaig>/Y	involves: 129 * C57BL/6	Y	26999603
MGI:5779971	M	MP:0012185	abnormal muscle precursor cell morphology	Kdm6a<tm2.1Kaig>/Y	involves: 129 * C57BL/6	N	26999603
MGI:5779972	F	MP:0012185	abnormal muscle precursor cell morphology	Kdm6a<tm2.1Kaig>/Kdm6a<tm2.1Kaig>	involves: 129 * C57BL/6	N	26999603
MGI:5779972	F	MP:0013239	impaired skeletal muscle regeneration	Kdm6a<tm2.1Kaig>/Kdm6a<tm2.1Kaig>	involves: 129 * C57BL/6	N	26999603
MGI:5779972	F	MP:0005369	muscle phenotype	Kdm6a<tm2.1Kaig>/Kdm6a<tm2.1Kaig>	involves: 129 * C57BL/6	Y	26999603
MGI:5780067	F	MP:0008177	increased germinal center B cell number	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	N	26366712
MGI:5780067	F	MP:0008211	decreased mature B cell number	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	N	26366712
MGI:5780067	F	MP:0005387	immune system phenotype	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	Y	26366712
MGI:5780067	F	MP:0005017	decreased B cell number	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	N	26366712
MGI:5780067	F	MP:0008174	decreased follicular B cell number	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	N	26366712
MGI:5780067	F	MP:0008495	decreased IgG1 level	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	N	26366712
MGI:5780067	F	MP:0001806	decreased IgM level	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	N	26366712
MGI:5780067	F	MP:0002144	abnormal B cell differentiation	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	N	26366712
MGI:5780067	F	MP:0008483	increased spleen germinal center size	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	N	26366712
MGI:5780067	F	MP:0008481	increased spleen germinal center number	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	N	26366712
MGI:5780067	F	MP:0005154	increased B cell proliferation	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	N	26366712
MGI:5780068	F	MP:0005387	immune system phenotype	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Ighg1<tm1(cre)Cgn>/Ighg1<+>	involves: 129P2/OlaHsd * C57BL/6	Y	26366712
MGI:5780069	F	MP:0008483	increased spleen germinal center size	Kmt2d<tm1.1Kaig>/Kmt2d<+>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	N	26366712
MGI:5780069	F	MP:0008177	increased germinal center B cell number	Kmt2d<tm1.1Kaig>/Kmt2d<+>,Cd19<tm1(cre)Cgn>/Cd19<+>	involves: 129P2/OlaHsd * C57BL/6	N	26366712
MGI:5780071	F	MP:0002023	increased B cell derived lymphoma incidence	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Ighg1<tm1(cre)Cgn>/Ighg1<+>,Tg(Vav-BCL2)69Jad/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	N	26366712
MGI:5780071	F	MP:0009317	increased follicular lymphoma incidence	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Ighg1<tm1(cre)Cgn>/Ighg1<+>,Tg(Vav-BCL2)69Jad/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	N	26366712
MGI:5780071	F	MP:0002083	premature death	Kmt2d<tm1.1Kaig>/Kmt2d<tm1.1Kaig>,Ighg1<tm1(cre)Cgn>/Ighg1<+>,Tg(Vav-BCL2)69Jad/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	N	26366712
MGI:5780072	F	MP:0002023	increased B cell derived lymphoma incidence	Kmt2d<tm1.1Kaig>/Kmt2d<+>,Ighg1<tm1(cre)Cgn>/Ighg1<+>,Tg(Vav-BCL2)69Jad/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	N	26366712
MGI:5780072	F	MP:0002083	premature death	Kmt2d<tm1.1Kaig>/Kmt2d<+>,Ighg1<tm1(cre)Cgn>/Ighg1<+>,Tg(Vav-BCL2)69Jad/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	N	26366712
MGI:5780072	F	MP:0009317	increased follicular lymphoma incidence	Kmt2d<tm1.1Kaig>/Kmt2d<+>,Ighg1<tm1(cre)Cgn>/Ighg1<+>,Tg(Vav-BCL2)69Jad/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	N	26366712
MGI:5780138	M	MP:0001925	male infertility	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0009831	abnormal sperm midpiece morphology	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0005578	teratozoospermia	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0001156	abnormal spermatogenesis	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0006380	abnormal spermatid morphology	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0002675	asthenozoospermia	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0009834	abnormal sperm annulus morphology	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0004182	abnormal spermiation	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0008892	abnormal sperm flagellum morphology	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0031410	biflagellated sperm	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0002662	abnormal cauda epididymis morphology	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0004543	abnormal sperm physiology	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	F	MP:0005389	reproductive system phenotype	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	Y	24244200
MGI:5780138	M	MP:0009238	coiled sperm flagellum	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0009230	abnormal sperm head morphology	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0001932	abnormal spermiogenesis	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0002687	oligozoospermia	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0020550	multinucleated giant male germ cells	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0013601	increased testis apoptosis	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780138	M	MP:0002660	abnormal caput epididymis morphology	Baz1a<tm1.1Sky>/Baz1a<tm1.1Sky>	involves: C57BL/6J * FVB/NJ	N	24244200
MGI:5780216	M	MP:0009133	decreased white fat cell size	Fmo5<tm1Eshe>/Fmo5<tm1Eshe>	B6.129P2-Fmo5<tm1Eshe>	N	26049045
MGI:5780216	M	MP:0014171	increased fatty acid oxidation	Fmo5<tm1Eshe>/Fmo5<tm1Eshe>	B6.129P2-Fmo5<tm1Eshe>	N	26049045
MGI:5780216	M	MP:0009289	decreased epididymal fat pad weight	Fmo5<tm1Eshe>/Fmo5<tm1Eshe>	B6.129P2-Fmo5<tm1Eshe>	N	26049045
MGI:5780553	F	MP:0002169	no abnormal phenotype detected	Gt(ROSA)26Sor<tm1(CAG-Errfi1)Jwj>/?,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25377472
MGI:5780554	F	MP:0002014	increased papilloma incidence	Gt(ROSA)26Sor<tm1(CAG-Errfi1)Jwj>/?,Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	25377472
MGI:5780554	F	MP:0009092	endometrium hyperplasia	Gt(ROSA)26Sor<tm1(CAG-Errfi1)Jwj>/?,Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	25377472
MGI:5780554	F	MP:0004904	increased uterus weight	Gt(ROSA)26Sor<tm1(CAG-Errfi1)Jwj>/?,Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	25377472
MGI:5780554	F	MP:0009671	abnormal uterus physiology	Gt(ROSA)26Sor<tm1(CAG-Errfi1)Jwj>/?,Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	25377472
MGI:5780554	F	MP:0002083	premature death	Gt(ROSA)26Sor<tm1(CAG-Errfi1)Jwj>/?,Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	25377472
MGI:5780568	M	MP:0005292	improved glucose tolerance	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0005289	increased oxygen consumption	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0001262	decreased body weight	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0005670	abnormal white adipose tissue physiology	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0008907	decreased total fat pad weight	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0008853	decreased abdominal adipose tissue amount	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0003960	increased lean body mass	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0003402	decreased liver weight	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0014146	decreased white adipose tissue mass	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0009356	decreased liver triglyceride level	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0009133	decreased white fat cell size	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0011581	increased triglyceride lipase activity	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0011699	abnormal brown adipose tissue thermogenesis	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0005659	decreased susceptibility to diet-induced obesity	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0020523	decreased susceptibility to induced hypothermia	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0014143	decreased body fat mass	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0002891	increased insulin sensitivity	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0010379	decreased respiratory quotient	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5780568	M	MP:0008034	enhanced lipolysis	G0s2<tm1Jgte>/G0s2<tm1Jgte>	involves: 129S7/SvEvBrd	N	25381555
MGI:5781017	M	MP:0008019	increased liver tumor incidence	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0003887	increased hepatocyte apoptosis	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0000607	abnormal hepatocyte morphology	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0010359	increased liver free fatty acids level	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0009355	increased liver triglyceride level	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0010027	increased liver cholesterol level	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0001654	hepatic necrosis	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0003331	increased hepatocellular carcinoma incidence	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0001860	liver inflammation	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0005141	liver hyperplasia	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0001573	abnormal circulating alanine transaminase level	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0003333	liver fibrosis	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0003324	increased liver adenoma incidence	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0008560	increased tumor necrosis factor secretion	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0002628	hepatic steatosis	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0008657	increased interleukin-1 beta secretion	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781017	M	MP:0009378	abnormal endoplasmic reticulum morphology	Tg(Mup3-Plau)350-2Eps/?	C57BL/6-Tg(Mup3-Plau)350-2Eps	N	25132496
MGI:5781552	M	MP:0000221	decreased leukocyte cell number	Slc23a4<tm1a(KOMP)Wtsi>/Slc23a4<tm1a(KOMP)Wtsi>	C57BL/6N-2010107G12Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781555	M	MP:0000455	abnormal maxilla morphology	Abhd5<tm1a(KOMP)Wtsi>/Abhd5<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Abhd5<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781556	M	MP:0001262	decreased body weight	Acsl4<tm1a(EUCOMM)Wtsi>/Y	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Acsl4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781556	M	MP:0003179	thrombocytopenia	Acsl4<tm1a(EUCOMM)Wtsi>/Y	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Acsl4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781556	M	MP:0000558	abnormal tibia morphology	Acsl4<tm1a(EUCOMM)Wtsi>/Y	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Acsl4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781557	F	MP:0003961	decreased lean body mass	Acsl4<tm1a(EUCOMM)Wtsi>/Acsl4<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Acsl4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781557	F	MP:0003179	thrombocytopenia	Acsl4<tm1a(EUCOMM)Wtsi>/Acsl4<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Acsl4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781557	F	MP:0001258	decreased body length	Acsl4<tm1a(EUCOMM)Wtsi>/Acsl4<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Acsl4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781557	F	MP:0002834	decreased heart weight	Acsl4<tm1a(EUCOMM)Wtsi>/Acsl4<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Acsl4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781558	M	MP:0002098	abnormal vibrissa morphology	Adam17<tm1a(EUCOMM)Wtsi>/Adam17<+>	B6JTyr;B6N-Adam17<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781561	F	MP:0002942	decreased circulating alanine transaminase level	Agtr2<tm1a(EUCOMM)Wtsi>/Agtr2<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Agtr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781561	F	MP:0001262	decreased body weight	Agtr2<tm1a(EUCOMM)Wtsi>/Agtr2<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Agtr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781561	F	MP:0000183	decreased circulating LDL cholesterol level	Agtr2<tm1a(EUCOMM)Wtsi>/Agtr2<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Agtr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781562	F	MP:0010087	increased circulating fructosamine level	Akap9<tm1a(KOMP)Wtsi>/Akap9<+>	B6JTyr;B6N-Akap9<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781562	M	MP:0000432	abnormal head morphology	Akap9<tm1a(KOMP)Wtsi>/Akap9<+>	B6JTyr;B6N-Akap9<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781562	M	MP:0010088	decreased circulating fructosamine level	Akap9<tm1a(KOMP)Wtsi>/Akap9<+>	B6JTyr;B6N-Akap9<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781563	F	MP:0004647	decreased lumbar vertebrae number	Akap9<tm1a(KOMP)Wtsi>/Akap9<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Akap9<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781564	M	MP:0002966	decreased circulating alkaline phosphatase level	Amfr<tm1a(KOMP)Wtsi>/Amfr<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Amfr<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781564	M	MP:0010088	decreased circulating fructosamine level	Amfr<tm1a(KOMP)Wtsi>/Amfr<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Amfr<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781564	M	MP:0005567	decreased circulating total protein level	Amfr<tm1a(KOMP)Wtsi>/Amfr<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Amfr<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781565	M	MP:0000218	increased leukocyte cell number	Ampd3<tm2a(KOMP)Wtsi>/Ampd3<tm2a(KOMP)Wtsi>	B6JTyr;B6N-Ampd3<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781565	F	MP:0004924	abnormal behavior	Ampd3<tm2a(KOMP)Wtsi>/Ampd3<tm2a(KOMP)Wtsi>	B6JTyr;B6N-Ampd3<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781566	F	MP:0002098	abnormal vibrissa morphology	Anks4b<tm2a(EUCOMM)Wtsi>/Anks4b<tm2a(EUCOMM)Wtsi>	B6JTyr;B6N-Anks4b<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781567	M	MP:0002697	abnormal eye size	Anxa6<tm1a(EUCOMM)Wtsi>/Anxa6<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Anxa6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781567	M	MP:0002098	abnormal vibrissa morphology	Anxa6<tm1a(EUCOMM)Wtsi>/Anxa6<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Anxa6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781568	M	MP:0000559	abnormal femur morphology	Ap4e1<tm1a(KOMP)Wtsi>/Ap4e1<tm1a(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781568	M	MP:0000062	increased bone mineral density	Ap4e1<tm1a(KOMP)Wtsi>/Ap4e1<tm1a(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781568	M	MP:0003960	increased lean body mass	Ap4e1<tm1a(KOMP)Wtsi>/Ap4e1<tm1a(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781569	M	MP:0000194	increased circulating calcium level	Arhgap18<tm1a(KOMP)Wtsi>/Arhgap18<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Arhgap18<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781571	M	MP:0004648	decreased thoracic vertebrae number	Arl4d<tm1a(EUCOMM)Wtsi>/Arl4d<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Arl4d<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781571	F	MP:0010124	decreased bone mineral content	Arl4d<tm1a(EUCOMM)Wtsi>/Arl4d<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Arl4d<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781571	M	MP:0000150	abnormal rib morphology	Arl4d<tm1a(EUCOMM)Wtsi>/Arl4d<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Arl4d<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781571	F	MP:0000063	decreased bone mineral density	Arl4d<tm1a(EUCOMM)Wtsi>/Arl4d<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Arl4d<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781571	M	MP:0004647	decreased lumbar vertebrae number	Arl4d<tm1a(EUCOMM)Wtsi>/Arl4d<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Arl4d<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781571	M	MP:0003345	decreased rib number	Arl4d<tm1a(EUCOMM)Wtsi>/Arl4d<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Arl4d<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781571	M	MP:0010101	increased sacral vertebrae number	Arl4d<tm1a(EUCOMM)Wtsi>/Arl4d<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Arl4d<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781572	M	MP:0002075	abnormal coat/hair pigmentation	Arpc2<tm1a(EUCOMM)Wtsi>/Arpc2<+>	B6JTyr;B6N-Arpc2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781573	M	MP:0002590	increased mean corpuscular volume	Arpc4<tm1a(EUCOMM)Wtsi>/Arpc4<+>	B6JTyr;B6N-Arpc4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781573	F	MP:0002074	abnormal hair texture	Arpc4<tm1a(EUCOMM)Wtsi>/Arpc4<+>	B6JTyr;B6N-Arpc4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781574	M	MP:0000221	decreased leukocyte cell number	Aste1<tm1a(KOMP)Wtsi>/Aste1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Aste1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781575	F	MP:0004609	vertebral fusion	Asxl1<tm1a(EUCOMM)Wtsi>/Asxl1<+>	B6Dnk;B6Brd;B6N-Asxl1<tm1a(EUCOMM)Wtsi> Tyr<c-Brd>/WtsiH	N	MGI:5285081
MGI:5781575	M	MP:0001314	cornea opacity	Asxl1<tm1a(EUCOMM)Wtsi>/Asxl1<+>	B6Dnk;B6Brd;B6N-Asxl1<tm1a(EUCOMM)Wtsi> Tyr<c-Brd>/WtsiH	N	MGI:5285081
MGI:5781575	M	MP:0001312	abnormal cornea morphology	Asxl1<tm1a(EUCOMM)Wtsi>/Asxl1<+>	B6Dnk;B6Brd;B6N-Asxl1<tm1a(EUCOMM)Wtsi> Tyr<c-Brd>/WtsiH	N	MGI:5285081
MGI:5781576	M	MP:0005561	increased mean corpuscular hemoglobin	Atg16l1<tm1a(EUCOMM)Wtsi>/Atg16l1<+>	C57BL/6N-Atg16l1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781578	M	MP:0004648	decreased thoracic vertebrae number	Atpaf2<tm1a(KOMP)Wtsi>/Atpaf2<+>	B6JTyr;B6N-Atpaf2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781578	M	MP:0000455	abnormal maxilla morphology	Atpaf2<tm1a(KOMP)Wtsi>/Atpaf2<+>	B6JTyr;B6N-Atpaf2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781578	M	MP:0000137	abnormal vertebrae morphology	Atpaf2<tm1a(KOMP)Wtsi>/Atpaf2<+>	B6JTyr;B6N-Atpaf2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781578	M	MP:0003345	decreased rib number	Atpaf2<tm1a(KOMP)Wtsi>/Atpaf2<+>	B6JTyr;B6N-Atpaf2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781578	M	MP:0001262	decreased body weight	Atpaf2<tm1a(KOMP)Wtsi>/Atpaf2<+>	B6JTyr;B6N-Atpaf2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781579	M	MP:0002966	decreased circulating alkaline phosphatase level	Atp5if1<tm1a(EUCOMM)Wtsi>/Atp5if1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Atp5if1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781580	M	MP:0000438	abnormal cranium morphology	Bbx<tm1a(EUCOMM)Wtsi>/Bbx<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Bbx<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781580	F	MP:0000063	decreased bone mineral density	Bbx<tm1a(EUCOMM)Wtsi>/Bbx<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Bbx<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781580	M	MP:0002100	abnormal tooth morphology	Bbx<tm1a(EUCOMM)Wtsi>/Bbx<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Bbx<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781581	M	MP:0010124	decreased bone mineral content	Cybc1<tm1a(KOMP)Wtsi>/Cybc1<tm1a(KOMP)Wtsi>	C57BL/6N-Cybc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781581	M	MP:0010025	decreased total body fat amount	Cybc1<tm1a(KOMP)Wtsi>/Cybc1<tm1a(KOMP)Wtsi>	C57BL/6N-Cybc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781581	M	MP:0001262	decreased body weight	Cybc1<tm1a(KOMP)Wtsi>/Cybc1<tm1a(KOMP)Wtsi>	C57BL/6N-Cybc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781581	M	MP:0008805	decreased circulating amylase level	Cybc1<tm1a(KOMP)Wtsi>/Cybc1<tm1a(KOMP)Wtsi>	C57BL/6N-Cybc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781585	F	MP:0001391	abnormal tail movements	Cadm1<tm1a(EUCOMM)Wtsi>/Cadm1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Cadm1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781586	M	MP:0004924	abnormal behavior	Cc2d1b<tm1a(KOMP)Wtsi>/Cc2d1b<tm1a(KOMP)Wtsi>	Not Specified	N	MGI:5285081
MGI:5781586	F	MP:0002702	decreased circulating free fatty acids level	Cc2d1b<tm1a(KOMP)Wtsi>/Cc2d1b<tm1a(KOMP)Wtsi>	Not Specified	N	MGI:4839251
MGI:5781588	F	MP:0005562	decreased mean corpuscular hemoglobin	Ccdc57<tm1a(EUCOMM)Wtsi>/Ccdc57<+>	B6JTyr;B6N-Ccdc57<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781589	F	MP:0000438	abnormal cranium morphology	Ccdc57<tm1a(EUCOMM)Wtsi>/Ccdc57<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Ccdc57<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781590	F	MP:0002968	increased circulating alkaline phosphatase level	Cdca8<tm1a(KOMP)Wtsi>/Cdca8<+>	C57BL/6N-Cdca8<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781590	M	MP:0003019	increased circulating chloride level	Cdca8<tm1a(KOMP)Wtsi>/Cdca8<+>	C57BL/6N-Cdca8<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781590	F	MP:0003020	decreased circulating chloride level	Cdca8<tm1a(KOMP)Wtsi>/Cdca8<+>	C57BL/6N-Cdca8<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781591	F	MP:0000432	abnormal head morphology	Cdk5rap2<tm1a(EUCOMM)Wtsi>/Cdk5rap2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cdk5rap2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781591	M	MP:0000438	abnormal cranium morphology	Cdk5rap2<tm1a(EUCOMM)Wtsi>/Cdk5rap2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cdk5rap2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781592	M	MP:0001303	abnormal lens morphology	Cdkn2a<tm1a(EUCOMM)Wtsi>/Cdkn2a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cdkn2a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781592	M	MP:0001304	cataract	Cdkn2a<tm1a(EUCOMM)Wtsi>/Cdkn2a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cdkn2a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781593	M	MP:0000559	abnormal femur morphology	Cenpj<tm1a(EUCOMM)Wtsi>/Cenpj<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Cenpj<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781593	M	MP:0004609	vertebral fusion	Cenpj<tm1a(EUCOMM)Wtsi>/Cenpj<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Cenpj<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781594	M	MP:0002966	decreased circulating alkaline phosphatase level	Cfap36<tm1a(EUCOMM)Wtsi>/Cfap36<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cfap36<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781594	F	MP:0005633	increased circulating sodium level	Cfap36<tm1a(EUCOMM)Wtsi>/Cfap36<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cfap36<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781596	M	MP:0001262	decreased body weight	Chd7<tm2a(EUCOMM)Wtsi>/Chd7<+>	129S5;B6N-Chd7<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781598	M	MP:0005632	decreased circulating aspartate transaminase level	Cog2<tm1a(KOMP)Wtsi>/Cog2<+>	B6JTyr;B6N-Cog2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781598	M	MP:0001262	decreased body weight	Cog2<tm1a(KOMP)Wtsi>/Cog2<+>	B6JTyr;B6N-Cog2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781598	M	MP:0005571	decreased lactate dehydrogenase level	Cog2<tm1a(KOMP)Wtsi>/Cog2<+>	B6JTyr;B6N-Cog2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781598	M	MP:0002942	decreased circulating alanine transaminase level	Cog2<tm1a(KOMP)Wtsi>/Cog2<+>	B6JTyr;B6N-Cog2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781598	F	MP:0002608	increased hematocrit	Cog2<tm1a(KOMP)Wtsi>/Cog2<+>	B6JTyr;B6N-Cog2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781598	M	MP:0001552	increased circulating triglyceride level	Cog2<tm1a(KOMP)Wtsi>/Cog2<+>	B6JTyr;B6N-Cog2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781598	M	MP:0005554	decreased circulating creatinine level	Cog2<tm1a(KOMP)Wtsi>/Cog2<+>	B6JTyr;B6N-Cog2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781600	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Crlf3<tm1a(KOMP)Wtsi>/Crlf3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Crlf3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781600	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Crlf3<tm1a(KOMP)Wtsi>/Crlf3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Crlf3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781601	M	MP:0000438	abnormal cranium morphology	Kat14<tm1a(KOMP)Wtsi>/Kat14<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kat14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781601	F	MP:0005542	cornea vascularization	Kat14<tm1a(KOMP)Wtsi>/Kat14<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kat14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781601	M	MP:0005176	eyelids fail to open	Kat14<tm1a(KOMP)Wtsi>/Kat14<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kat14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781601	M	MP:0000455	abnormal maxilla morphology	Kat14<tm1a(KOMP)Wtsi>/Kat14<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kat14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781601	M	MP:0003671	abnormal eyelid aperture	Kat14<tm1a(KOMP)Wtsi>/Kat14<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kat14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781601	F	MP:0002874	decreased hemoglobin content	Kat14<tm1a(KOMP)Wtsi>/Kat14<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kat14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781601	M	MP:0001322	abnormal iris morphology	Kat14<tm1a(KOMP)Wtsi>/Kat14<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kat14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781601	F	MP:0001312	abnormal cornea morphology	Kat14<tm1a(KOMP)Wtsi>/Kat14<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kat14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781601	M	MP:0002100	abnormal tooth morphology	Kat14<tm1a(KOMP)Wtsi>/Kat14<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kat14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781601	F	MP:0010101	increased sacral vertebrae number	Kat14<tm1a(KOMP)Wtsi>/Kat14<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kat14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781601	M	MP:0002697	abnormal eye size	Kat14<tm1a(KOMP)Wtsi>/Kat14<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kat14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781602	F	MP:0010092	increased circulating magnesium level	Cyb561<tm1a(EUCOMM)Wtsi>/Cyb561<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Cyb561<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781602	M	MP:0000183	decreased circulating LDL cholesterol level	Cyb561<tm1a(EUCOMM)Wtsi>/Cyb561<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Cyb561<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781602	M	MP:0002075	abnormal coat/hair pigmentation	Cyb561<tm1a(EUCOMM)Wtsi>/Cyb561<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Cyb561<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781602	F	MP:0004924	abnormal behavior	Cyb561<tm1a(EUCOMM)Wtsi>/Cyb561<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Cyb561<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781603	F	MP:0001303	abnormal lens morphology	Dctn5<tm2a(KOMP)Wtsi>/Dctn5<+>	B6JTyr;B6N-Dctn5<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781603	M	MP:0004924	abnormal behavior	Dctn5<tm2a(KOMP)Wtsi>/Dctn5<+>	B6JTyr;B6N-Dctn5<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781603	M	MP:0000208	decreased hematocrit	Dctn5<tm2a(KOMP)Wtsi>/Dctn5<+>	B6JTyr;B6N-Dctn5<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781603	F	MP:0002608	increased hematocrit	Dctn5<tm2a(KOMP)Wtsi>/Dctn5<+>	B6JTyr;B6N-Dctn5<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781603	F	MP:0001304	cataract	Dctn5<tm2a(KOMP)Wtsi>/Dctn5<+>	B6JTyr;B6N-Dctn5<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781605	M	MP:0002702	decreased circulating free fatty acids level	Dip2b<tm1a(EUCOMM)Wtsi>/Dip2b<+>	B6JTyr;B6N-Dip2b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781607	M	MP:0004651	increased thoracic vertebrae number	Dscc1<tm1a(KOMP)Wtsi>/Dscc1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Dscc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781607	M	MP:0004609	vertebral fusion	Dscc1<tm1a(KOMP)Wtsi>/Dscc1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Dscc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781607	M	MP:0005565	increased blood urea nitrogen level	Dscc1<tm1a(KOMP)Wtsi>/Dscc1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Dscc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781607	F	MP:0000150	abnormal rib morphology	Dscc1<tm1a(KOMP)Wtsi>/Dscc1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Dscc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781609	F	MP:0003961	decreased lean body mass	Dusp26<tm1a(KOMP)Wtsi>/Dusp26<tm1a(KOMP)Wtsi>	C57BL/6N-Dusp26<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781609	M	MP:0003960	increased lean body mass	Dusp26<tm1a(KOMP)Wtsi>/Dusp26<tm1a(KOMP)Wtsi>	C57BL/6N-Dusp26<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781611	M	MP:0005634	decreased circulating sodium level	Dusp4<tm1a(EUCOMM)Wtsi>/Dusp4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dusp4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781611	M	MP:0004648	decreased thoracic vertebrae number	Dusp4<tm1a(EUCOMM)Wtsi>/Dusp4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dusp4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781611	F	MP:0010101	increased sacral vertebrae number	Dusp4<tm1a(EUCOMM)Wtsi>/Dusp4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dusp4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781611	F	MP:0004647	decreased lumbar vertebrae number	Dusp4<tm1a(EUCOMM)Wtsi>/Dusp4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dusp4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781611	F	MP:0005633	increased circulating sodium level	Dusp4<tm1a(EUCOMM)Wtsi>/Dusp4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dusp4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781611	F	MP:0005560	decreased circulating glucose level	Dusp4<tm1a(EUCOMM)Wtsi>/Dusp4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dusp4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781611	F	MP:0001539	decreased caudal vertebrae number	Dusp4<tm1a(EUCOMM)Wtsi>/Dusp4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dusp4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781612	M	MP:0005179	decreased circulating cholesterol level	Dync1i2<tm1a(EUCOMM)Wtsi>/Dync1i2<+>	C57BL/6N-Dync1i2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781612	F	MP:0005634	decreased circulating sodium level	Dync1i2<tm1a(EUCOMM)Wtsi>/Dync1i2<+>	C57BL/6N-Dync1i2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781612	M	MP:0010025	decreased total body fat amount	Dync1i2<tm1a(EUCOMM)Wtsi>/Dync1i2<+>	C57BL/6N-Dync1i2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781613	M	MP:0001529	abnormal vocalization	Efna1<tm1a(EUCOMM)Wtsi>/Efna1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Efna1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781614	M	MP:0000221	decreased leukocyte cell number	Egfr<tm1a(EUCOMM)Wtsi>/Egfr<+>	C57BL/6N-Egfr<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781615	F	MP:0003019	increased circulating chloride level	Ehd1<tm1a(EUCOMM)Wtsi>/Ehd1<+>	C57BL/6N-Ehd1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781616	M	MP:0003671	abnormal eyelid aperture	Ehd1<tm1a(EUCOMM)Wtsi>/Ehd1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ehd1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781618	M	MP:0000186	decreased circulating HDL cholesterol level	Eif4e3<tm1a(KOMP)Wtsi>/Eif4e3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Eif4e3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781618	F	MP:0001406	abnormal gait	Eif4e3<tm1a(KOMP)Wtsi>/Eif4e3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Eif4e3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781618	M	MP:0000183	decreased circulating LDL cholesterol level	Eif4e3<tm1a(KOMP)Wtsi>/Eif4e3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Eif4e3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781618	M	MP:0005179	decreased circulating cholesterol level	Eif4e3<tm1a(KOMP)Wtsi>/Eif4e3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Eif4e3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781618	M	MP:0000195	decreased circulating calcium level	Eif4e3<tm1a(KOMP)Wtsi>/Eif4e3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Eif4e3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781619	M	MP:0000221	decreased leukocyte cell number	Epc1<tm1a(EUCOMM)Wtsi>/Epc1<+>	Not Specified	N	MGI:5285081
MGI:5781619	F	MP:0004924	abnormal behavior	Epc1<tm1a(EUCOMM)Wtsi>/Epc1<+>	Not Specified	N	MGI:5285081
MGI:5781619	M	MP:0003062	abnormal coping response	Epc1<tm1a(EUCOMM)Wtsi>/Epc1<+>	Not Specified	N	MGI:4839251
MGI:5781620	F	MP:0005562	decreased mean corpuscular hemoglobin	Eps15<tm1a(KOMP)Wtsi>/Eps15<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Eps15<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781623	M	MP:0001552	increased circulating triglyceride level	Ezh2<tm1a(EUCOMM)Wtsi>/Ezh2<+>	C57BL/6N-Ezh2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781623	F	MP:0010101	increased sacral vertebrae number	Ezh2<tm1a(EUCOMM)Wtsi>/Ezh2<+>	C57BL/6N-Ezh2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781624	M	MP:0003960	increased lean body mass	Fahd2a<tm1a(EUCOMM)Wtsi>/Fahd2a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fahd2a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781624	M	MP:0000062	increased bone mineral density	Fahd2a<tm1a(EUCOMM)Wtsi>/Fahd2a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fahd2a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781625	F	MP:0005343	increased circulating aspartate transaminase level	Vcf1<tm2a(EUCOMM)Wtsi>/Vcf1<tm2a(EUCOMM)Wtsi>	B6JTyr;B6N-Vcf1<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781625	F	MP:0004924	abnormal behavior	Vcf1<tm2a(EUCOMM)Wtsi>/Vcf1<tm2a(EUCOMM)Wtsi>	B6JTyr;B6N-Vcf1<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781626	F	MP:0001262	decreased body weight	Fam107b<tm1a(KOMP)Wtsi>/Fam107b<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Fam107b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781626	F	MP:0000367	abnormal coat/ hair morphology	Fam107b<tm1a(KOMP)Wtsi>/Fam107b<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Fam107b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781626	F	MP:0000452	abnormal mouth morphology	Fam107b<tm1a(KOMP)Wtsi>/Fam107b<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Fam107b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781627	F	MP:0000063	decreased bone mineral density	Miga2<tm1a(KOMP)Wtsi>/Miga2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Miga2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781627	M	MP:0002874	decreased hemoglobin content	Miga2<tm1a(KOMP)Wtsi>/Miga2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Miga2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781627	M	MP:0000455	abnormal maxilla morphology	Miga2<tm1a(KOMP)Wtsi>/Miga2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Miga2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781627	M	MP:0005571	decreased lactate dehydrogenase level	Miga2<tm1a(KOMP)Wtsi>/Miga2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Miga2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781627	M	MP:0000208	decreased hematocrit	Miga2<tm1a(KOMP)Wtsi>/Miga2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Miga2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781627	M	MP:0002100	abnormal tooth morphology	Miga2<tm1a(KOMP)Wtsi>/Miga2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Miga2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781627	M	MP:0000443	abnormal snout morphology	Miga2<tm1a(KOMP)Wtsi>/Miga2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Miga2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781627	M	MP:0000438	abnormal cranium morphology	Miga2<tm1a(KOMP)Wtsi>/Miga2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Miga2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781629	M	MP:0002095	abnormal skin pigmentation	Fryl<tm1a(KOMP)Wtsi>/Fryl<+>	C57BL/6N-Fryl<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781630	F	MP:0001399	hyperactivity	Fto<tm1a(EUCOMM)Wtsi>/Fto<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Fto<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781630	M	MP:0005571	decreased lactate dehydrogenase level	Fto<tm1a(EUCOMM)Wtsi>/Fto<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Fto<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781630	M	MP:0000183	decreased circulating LDL cholesterol level	Fto<tm1a(EUCOMM)Wtsi>/Fto<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Fto<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781632	F	MP:0001554	increased circulating free fatty acids level	Gfm1<tm1a(EUCOMM)Wtsi>/Gfm1<+>	C57BL/6N-Gfm1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781633	F	MP:0003179	thrombocytopenia	Grin1<tm1a(EUCOMM)Wtsi>/Grin1<+>	C57BL/6N-Grin1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781634	F	MP:0001258	decreased body length	Gsk3a<tm1a(EUCOMM)Wtsi>/Gsk3a<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Gsk3a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781634	M	MP:0010101	increased sacral vertebrae number	Gsk3a<tm1a(EUCOMM)Wtsi>/Gsk3a<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Gsk3a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781634	M	MP:0004647	decreased lumbar vertebrae number	Gsk3a<tm1a(EUCOMM)Wtsi>/Gsk3a<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Gsk3a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781635	F	MP:0002098	abnormal vibrissa morphology	Gys2<tm1a(KOMP)Wtsi>/Gys2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Gys2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781635	F	MP:0003442	decreased circulating glycerol level	Gys2<tm1a(KOMP)Wtsi>/Gys2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Gys2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781636	M	MP:0003960	increased lean body mass	H2-M5<tm1(KOMP)Wtsi>/H2-M5<tm1(KOMP)Wtsi>	C57BL/6N-H2-M5<tm1(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781637	M	MP:0001258	decreased body length	Hdac8<tm1a(EUCOMM)Wtsi>/Y	C57BL/6N-Hdac8<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781637	M	MP:0000063	decreased bone mineral density	Hdac8<tm1a(EUCOMM)Wtsi>/Y	C57BL/6N-Hdac8<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781638	F	MP:0010124	decreased bone mineral content	Hdac8<tm1a(EUCOMM)Wtsi>/Hdac8<tm1a(EUCOMM)Wtsi>	C57BL/6N-Hdac8<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781638	F	MP:0000063	decreased bone mineral density	Hdac8<tm1a(EUCOMM)Wtsi>/Hdac8<tm1a(EUCOMM)Wtsi>	C57BL/6N-Hdac8<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781639	M	MP:0001391	abnormal tail movements	Herc3<tm1a(EUCOMM)Wtsi>/Herc3<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Herc3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781639	F	MP:0000745	tremors	Herc3<tm1a(EUCOMM)Wtsi>/Herc3<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Herc3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781639	F	MP:0004924	abnormal behavior	Herc3<tm1a(EUCOMM)Wtsi>/Herc3<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Herc3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781640	F	MP:0003345	decreased rib number	Hira<tm1a(EUCOMM)Wtsi>/Hira<+>	C57BL/6N-Hira<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781641	F	MP:0004924	abnormal behavior	Ift25<tm1a(EUCOMM)Wtsi>/Ift25<+>	B6JTyr;B6N-Ift25<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781641	F	MP:0001554	increased circulating free fatty acids level	Ift25<tm1a(EUCOMM)Wtsi>/Ift25<+>	B6JTyr;B6N-Ift25<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781641	F	MP:0003443	increased circulating glycerol level	Ift25<tm1a(EUCOMM)Wtsi>/Ift25<+>	B6JTyr;B6N-Ift25<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781642	M	MP:0000455	abnormal maxilla morphology	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Ide<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781642	M	MP:0000438	abnormal cranium morphology	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Ide<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781642	M	MP:0008806	increased circulating amylase level	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Ide<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781642	M	MP:0005358	abnormal incisor morphology	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Ide<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781642	M	MP:0002833	increased heart weight	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Ide<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781642	F	MP:0002074	abnormal hair texture	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Ide<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781643	F	MP:0005419	decreased circulating serum albumin level	Il22ra1<tm1a(EUCOMM)Wtsi>/Il22ra1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Il22ra1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781644	M	MP:0001260	increased body weight	Inpp1<tm1a(KOMP)Wtsi>/Inpp1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Inpp1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781644	F	MP:0001262	decreased body weight	Inpp1<tm1a(KOMP)Wtsi>/Inpp1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Inpp1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781645	F	MP:0010092	increased circulating magnesium level	Ints12<tm1a(EUCOMM)Wtsi>/Ints12<+>	B6JTyr;B6N-Ints12<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781646	F	MP:0005553	increased circulating creatinine level	Jarid2<tm1a(KOMP)Wtsi>/Jarid2<+>	Not Specified	N	MGI:5285081
MGI:5781648	M	MP:0002875	decreased erythrocyte cell number	Kcne2<tm1a(EUCOMM)Wtsi>/Kcne2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kcne2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781649	M	MP:0008535	enlarged lateral ventricles	Kdm4b<tm1a(EUCOMM)Wtsi>/Kdm4b<+>	B6Dnk;B6Brd;B6N-Tyr<c-Brd> Kdm4b<tm1a(EUCOMM)Wtsi>/WtsiH	N	33232677
MGI:5781649	M	MP:0002196	absent corpus callosum	Kdm4b<tm1a(EUCOMM)Wtsi>/Kdm4b<+>	B6Dnk;B6Brd;B6N-Tyr<c-Brd> Kdm4b<tm1a(EUCOMM)Wtsi>/WtsiH	N	33232677
MGI:5781649	M	MP:0012460	decreased dentate gyrus size	Kdm4b<tm1a(EUCOMM)Wtsi>/Kdm4b<+>	B6Dnk;B6Brd;B6N-Tyr<c-Brd> Kdm4b<tm1a(EUCOMM)Wtsi>/WtsiH	N	33232677
MGI:5781649	M	MP:0000771	abnormal brain size	Kdm4b<tm1a(EUCOMM)Wtsi>/Kdm4b<+>	B6Dnk;B6Brd;B6N-Tyr<c-Brd> Kdm4b<tm1a(EUCOMM)Wtsi>/WtsiH	N	33232677
MGI:5781651	F	MP:0001413	abnormal response to new environment	Kng2<tm2a(EUCOMM)Wtsi>/Kng2<tm2a(EUCOMM)Wtsi>	C57BL/6N-Kng2<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5781651	M	MP:0005553	increased circulating creatinine level	Kng2<tm2a(EUCOMM)Wtsi>/Kng2<tm2a(EUCOMM)Wtsi>	C57BL/6N-Kng2<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5781651	M	MP:0001257	increased body length	Kng2<tm2a(EUCOMM)Wtsi>/Kng2<tm2a(EUCOMM)Wtsi>	C57BL/6N-Kng2<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781654	M	MP:0010025	decreased total body fat amount	Ldha<tm1a(EUCOMM)Wtsi>/Ldha<+>	B6JTyr;B6N-Ldha<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781654	M	MP:0002966	decreased circulating alkaline phosphatase level	Ldha<tm1a(EUCOMM)Wtsi>/Ldha<+>	B6JTyr;B6N-Ldha<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781654	M	MP:0002942	decreased circulating alanine transaminase level	Ldha<tm1a(EUCOMM)Wtsi>/Ldha<+>	B6JTyr;B6N-Ldha<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781654	M	MP:0000186	decreased circulating HDL cholesterol level	Ldha<tm1a(EUCOMM)Wtsi>/Ldha<+>	B6JTyr;B6N-Ldha<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781656	M	MP:0005553	increased circulating creatinine level	Lmnb2<tm1a(KOMP)Wtsi>/Lmnb2<+>	B6JTyr;B6N-Lmnb2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781657	F	MP:0001258	decreased body length	Lrig1<tm1a(EUCOMM)Wtsi>/Lrig1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Lrig1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781657	F	MP:0002111	abnormal tail morphology	Lrig1<tm1a(EUCOMM)Wtsi>/Lrig1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Lrig1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781657	M	MP:0004924	abnormal behavior	Lrig1<tm1a(EUCOMM)Wtsi>/Lrig1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Lrig1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781661	M	MP:0000438	abnormal cranium morphology	Ltbp1<tm1a(EUCOMM)Wtsi>/Ltbp1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Ltbp1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781661	M	MP:0005358	abnormal incisor morphology	Ltbp1<tm1a(EUCOMM)Wtsi>/Ltbp1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Ltbp1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781663	F	MP:0001406	abnormal gait	Map2k2<tm1a(EUCOMM)Wtsi>/Map2k2<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Map2k2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781665	F	MP:0000063	decreased bone mineral density	Mcph1<tm1a(EUCOMM)Wtsi>/Mcph1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Mcph1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781665	F	MP:0001312	abnormal cornea morphology	Mcph1<tm1a(EUCOMM)Wtsi>/Mcph1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Mcph1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781665	F	MP:0001314	cornea opacity	Mcph1<tm1a(EUCOMM)Wtsi>/Mcph1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Mcph1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781665	F	MP:0001324	abnormal eye pigmentation	Mcph1<tm1a(EUCOMM)Wtsi>/Mcph1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Mcph1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781665	F	MP:0005542	cornea vascularization	Mcph1<tm1a(EUCOMM)Wtsi>/Mcph1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Mcph1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781667	M	MP:0002590	increased mean corpuscular volume	Mgst3<tm1a(KOMP)Wtsi>/Mgst3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Mgst3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781667	F	MP:0002591	decreased mean corpuscular volume	Mgst3<tm1a(KOMP)Wtsi>/Mgst3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Mgst3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781668	M	MP:0001262	decreased body weight	Mier1<tm1a(EUCOMM)Wtsi>/Mier1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Mier1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781668	M	MP:0001262	decreased body weight	Mier1<tm1a(EUCOMM)Wtsi>/Mier1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Mier1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781668	M	MP:0002702	decreased circulating free fatty acids level	Mier1<tm1a(EUCOMM)Wtsi>/Mier1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Mier1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781668	F	MP:0001529	abnormal vocalization	Mier1<tm1a(EUCOMM)Wtsi>/Mier1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Mier1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781669	F	MP:0002111	abnormal tail morphology	Mis18bp1<tm1a(EUCOMM)Wtsi>/Mis18bp1<+>	B6JTyr;B6N-Mis18bp1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781670	F	MP:0000579	abnormal nail morphology	Mks1<tm1a(EUCOMM)Wtsi>/Mks1<+>	B6JTyr;B6N-Mks1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781671	F	MP:0006358	absent pinna reflex	Mms22l<tm1a(EUCOMM)Wtsi>/Mms22l<+>	B6JTyr;B6N-Mms22l<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781674	F	MP:0002896	abnormal bone mineralization	Mta1<tm1a(EUCOMM)Wtsi>/Mta1<tm1a(EUCOMM)Wtsi>	129S/SvEvBrd-Mta1<tm1a(EUCOMM)Wtsi>/WtsiH	N	MGI:5285081
MGI:5781674	M	MP:0000183	decreased circulating LDL cholesterol level	Mta1<tm1a(EUCOMM)Wtsi>/Mta1<tm1a(EUCOMM)Wtsi>	129S/SvEvBrd-Mta1<tm1a(EUCOMM)Wtsi>/WtsiH	N	MGI:5285081
MGI:5781675	M	MP:0000183	decreased circulating LDL cholesterol level	Mtor<tm1a(EUCOMM)Wtsi>/Mtor<+>	C57BL/6N-Mtor<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781675	F	MP:0000182	increased circulating LDL cholesterol level	Mtor<tm1a(EUCOMM)Wtsi>/Mtor<+>	C57BL/6N-Mtor<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781676	M	MP:0003960	increased lean body mass	Mx1<tm1a(EUCOMM)Wtsi>/Mx1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mx1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781677	F	MP:0001260	increased body weight	Myd88<tm1a(EUCOMM)Wtsi>/Myd88<tm1a(EUCOMM)Wtsi>	C57BL/6N-Myd88<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781678	F	MP:0005562	decreased mean corpuscular hemoglobin	Myl12b<tm1a(EUCOMM)Wtsi>/Myl12b<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Myl12b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781678	F	MP:0005565	increased blood urea nitrogen level	Myl12b<tm1a(EUCOMM)Wtsi>/Myl12b<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Myl12b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781679	M	MP:0002075	abnormal coat/hair pigmentation	Myo5a<tm1a(KOMP)Wtsi>/Myo5a<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Myo5a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781680	M	MP:0008806	increased circulating amylase level	Ncaph2<tm1a(EUCOMM)Wtsi>/Ncaph2<+>	B6JTyr;B6N-Ncaph2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781681	M	MP:0005571	decreased lactate dehydrogenase level	Ndufs3<tm1a(EUCOMM)Wtsi>/Ndufs3<+>	B6JTyr;B6N-Ndufs3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781681	M	MP:0002833	increased heart weight	Ndufs3<tm1a(EUCOMM)Wtsi>/Ndufs3<+>	B6JTyr;B6N-Ndufs3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781682	F	MP:0001260	increased body weight	Nf1<tm1a(KOMP)Wtsi>/Nf1<+>	B6JTyr;B6N-Nf1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781683	M	MP:0005634	decreased circulating sodium level	Nfkb1<tm1a(KOMP)Wtsi>/Nfkb1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Nfkb1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781683	F	MP:0001191	abnormal skin condition	Nfkb1<tm1a(KOMP)Wtsi>/Nfkb1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Nfkb1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781683	F	MP:0001312	abnormal cornea morphology	Nfkb1<tm1a(KOMP)Wtsi>/Nfkb1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Nfkb1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781683	F	MP:0002968	increased circulating alkaline phosphatase level	Nfkb1<tm1a(KOMP)Wtsi>/Nfkb1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Nfkb1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781683	F	MP:0003998	decreased thermal nociceptive threshold	Nfkb1<tm1a(KOMP)Wtsi>/Nfkb1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Nfkb1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781683	M	MP:0001973	increased thermal nociceptive threshold	Nfkb1<tm1a(KOMP)Wtsi>/Nfkb1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Nfkb1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781683	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Nfkb1<tm1a(KOMP)Wtsi>/Nfkb1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Nfkb1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781683	M	MP:0003961	decreased lean body mass	Nfkb1<tm1a(KOMP)Wtsi>/Nfkb1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Nfkb1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781685	M	MP:0000186	decreased circulating HDL cholesterol level	Nipa1<tm1a(KOMP)Wtsi>/Nipa1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Nipa1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781687	F	MP:0002591	decreased mean corpuscular volume	Nsun2<tm1a(EUCOMM)Wtsi>/Nsun2<+>	B6JTyr;B6N-Nsun2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781687	F	MP:0001349	excessive tearing	Nsun2<tm1a(EUCOMM)Wtsi>/Nsun2<+>	B6JTyr;B6N-Nsun2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781688	M	MP:0000443	abnormal snout morphology	Nsun2<tm1a(EUCOMM)Wtsi>/Nsun2<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Nsun2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781688	M	MP:0000438	abnormal cranium morphology	Nsun2<tm1a(EUCOMM)Wtsi>/Nsun2<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Nsun2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781688	M	MP:0002100	abnormal tooth morphology	Nsun2<tm1a(EUCOMM)Wtsi>/Nsun2<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Nsun2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781688	F	MP:0002932	abnormal joint morphology	Nsun2<tm1a(EUCOMM)Wtsi>/Nsun2<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Nsun2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781689	M	MP:0005560	decreased circulating glucose level	Oasl2<tm1a(EUCOMM)Wtsi>/Oasl2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Oasl2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781690	M	MP:0001191	abnormal skin condition	Ogfod1<tm1a(KOMP)Wtsi>/Ogfod1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Ogfod1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781690	M	MP:0004151	decreased circulating iron level	Ogfod1<tm1a(KOMP)Wtsi>/Ogfod1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Ogfod1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781690	M	MP:0000559	abnormal femur morphology	Ogfod1<tm1a(KOMP)Wtsi>/Ogfod1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Ogfod1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781691	F	MP:0000186	decreased circulating HDL cholesterol level	Optn<tm1a(EUCOMM)Wtsi>/Optn<tm1a(EUCOMM)Wtsi>	C57BL/6N-Optn<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781692	F	MP:0001926	female infertility	Pabpc1l<tm1a(EUCOMM)Wtsi>/Pabpc1l<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pabpc1l<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5781693	M	MP:0010088	decreased circulating fructosamine level	Pex3<tm1a(EUCOMM)Wtsi>/Pex3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pex3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781693	M	MP:0005419	decreased circulating serum albumin level	Pex3<tm1a(EUCOMM)Wtsi>/Pex3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pex3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781693	F	MP:0010087	increased circulating fructosamine level	Pex3<tm1a(EUCOMM)Wtsi>/Pex3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pex3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781695	M	MP:0004647	decreased lumbar vertebrae number	Pik3cb<tm1a(EUCOMM)Wtsi>/Pik3cb<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Pik3cb<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781696	M	MP:0002942	decreased circulating alanine transaminase level	Pik3cg<tm1a(EUCOMM)Wtsi>/Pik3cg<tm1a(EUCOMM)Wtsi>	B6NTac;B6N-A<tm1Brd> Pik3cg<tm1a(EUCOMM)Wtsi>/WtsiOulu	N	MGI:5285081
MGI:5781698	F	MP:0005561	increased mean corpuscular hemoglobin	Pitpnm1<tm1a(EUCOMM)Wtsi>/Pitpnm1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pitpnm1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781699	F	MP:0010087	increased circulating fructosamine level	Plekhg1<tm1a(EUCOMM)Wtsi>/Plekhg1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Plekhg1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781700	F	MP:0000218	increased leukocyte cell number	Plekhm2<tm1a(EUCOMM)Wtsi>/Plekhm2<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Plekhm2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781701	F	MP:0004647	decreased lumbar vertebrae number	Polr1e<tm1a(KOMP)Wtsi>/Polr1e<+>	B6JTyr;B6N-Polr1e<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781701	M	MP:0004924	abnormal behavior	Polr1e<tm1a(KOMP)Wtsi>/Polr1e<+>	B6JTyr;B6N-Polr1e<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781701	F	MP:0010101	increased sacral vertebrae number	Polr1e<tm1a(KOMP)Wtsi>/Polr1e<+>	B6JTyr;B6N-Polr1e<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781701	M	MP:0003345	decreased rib number	Polr1e<tm1a(KOMP)Wtsi>/Polr1e<+>	B6JTyr;B6N-Polr1e<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781701	M	MP:0001262	decreased body weight	Polr1e<tm1a(KOMP)Wtsi>/Polr1e<+>	B6JTyr;B6N-Polr1e<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781703	M	MP:0002644	decreased circulating triglyceride level	Ppp5c<tm1a(EUCOMM)Wtsi>/Ppp5c<tm1a(EUCOMM)Wtsi>	B6Dnk;B6Brd;B6N-Ppp5c<tm1a(EUCOMM)Wtsi> Tyr<c-Brd>/WtsiH	N	MGI:5285081
MGI:5781703	F	MP:0004647	decreased lumbar vertebrae number	Ppp5c<tm1a(EUCOMM)Wtsi>/Ppp5c<tm1a(EUCOMM)Wtsi>	B6Dnk;B6Brd;B6N-Ppp5c<tm1a(EUCOMM)Wtsi> Tyr<c-Brd>/WtsiH	N	MGI:4839251
MGI:5781703	F	MP:0000150	abnormal rib morphology	Ppp5c<tm1a(EUCOMM)Wtsi>/Ppp5c<tm1a(EUCOMM)Wtsi>	B6Dnk;B6Brd;B6N-Ppp5c<tm1a(EUCOMM)Wtsi> Tyr<c-Brd>/WtsiH	N	MGI:4839251
MGI:5781703	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Ppp5c<tm1a(EUCOMM)Wtsi>/Ppp5c<tm1a(EUCOMM)Wtsi>	B6Dnk;B6Brd;B6N-Ppp5c<tm1a(EUCOMM)Wtsi> Tyr<c-Brd>/WtsiH	N	MGI:5285081
MGI:5781703	F	MP:0004924	abnormal behavior	Ppp5c<tm1a(EUCOMM)Wtsi>/Ppp5c<tm1a(EUCOMM)Wtsi>	B6Dnk;B6Brd;B6N-Ppp5c<tm1a(EUCOMM)Wtsi> Tyr<c-Brd>/WtsiH	N	MGI:5285081
MGI:5781706	M	MP:0002968	increased circulating alkaline phosphatase level	Prkcz<tm1a(EUCOMM)Wtsi>/Prkcz<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Prkcz<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781706	M	MP:0005343	increased circulating aspartate transaminase level	Prkcz<tm1a(EUCOMM)Wtsi>/Prkcz<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Prkcz<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781706	M	MP:0002941	increased circulating alanine transaminase level	Prkcz<tm1a(EUCOMM)Wtsi>/Prkcz<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Prkcz<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781708	M	MP:0010101	increased sacral vertebrae number	Prmt2<tm1a(EUCOMM)Wtsi>/Prmt2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Prmt2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781709	M	MP:0010101	increased sacral vertebrae number	Prmt3<tm1a(EUCOMM)Wtsi>/Prmt3<+>	B6JTyr;B6N-Prmt3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781711	F	MP:0000150	abnormal rib morphology	Prmt7<tm1a(EUCOMM)Wtsi>/Prmt7<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Prmt7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781711	M	MP:0002875	decreased erythrocyte cell number	Prmt7<tm1a(EUCOMM)Wtsi>/Prmt7<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Prmt7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781714	M	MP:0003961	decreased lean body mass	Pxylp1<tm1a(KOMP)Wtsi>/Pxylp1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Pxylp1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781714	M	MP:0005562	decreased mean corpuscular hemoglobin	Pxylp1<tm1a(KOMP)Wtsi>/Pxylp1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Pxylp1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781714	M	MP:0001258	decreased body length	Pxylp1<tm1a(KOMP)Wtsi>/Pxylp1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Pxylp1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781714	F	MP:0001260	increased body weight	Pxylp1<tm1a(KOMP)Wtsi>/Pxylp1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Pxylp1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781714	M	MP:0001262	decreased body weight	Pxylp1<tm1a(KOMP)Wtsi>/Pxylp1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Pxylp1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781714	M	MP:0010124	decreased bone mineral content	Pxylp1<tm1a(KOMP)Wtsi>/Pxylp1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Pxylp1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781715	F	MP:0002074	abnormal hair texture	Rad18<tm1a(EUCOMM)Wtsi>/Rad18<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Rad18<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781715	M	MP:0000367	abnormal coat/ hair morphology	Rad18<tm1a(EUCOMM)Wtsi>/Rad18<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Rad18<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781715	M	MP:0010025	decreased total body fat amount	Rad18<tm1a(EUCOMM)Wtsi>/Rad18<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Rad18<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781717	M	MP:0001556	increased circulating HDL cholesterol level	Rars2<tm1a(EUCOMM)Wtsi>/Rars2<+>	B6JTyr;B6N-Rars2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781717	F	MP:0004924	abnormal behavior	Rars2<tm1a(EUCOMM)Wtsi>/Rars2<+>	B6JTyr;B6N-Rars2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781718	M	MP:0001973	increased thermal nociceptive threshold	Rars1<tm1a(EUCOMM)Wtsi>/Rars1<+>	C57BL/6N-Rars1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781719	M	MP:0002100	abnormal tooth morphology	Rbbp7<tm1a(EUCOMM)Wtsi>/Y	B6JTyr;B6N-Rbbp7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781719	M	MP:0000455	abnormal maxilla morphology	Rbbp7<tm1a(EUCOMM)Wtsi>/Y	B6JTyr;B6N-Rbbp7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781720	M	MP:0005627	increased circulating potassium level	Rdh16<tm1a(KOMP)Wtsi>/Rdh16<tm1a(KOMP)Wtsi>	C57BL/6N-Rdh16<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781721	F	MP:0001191	abnormal skin condition	Rhd<tm1a(EUCOMM)Wtsi>/Rhd<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Rhd<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781722	M	MP:0002932	abnormal joint morphology	Rhobtb3<tm1a(KOMP)Wtsi>/Rhobtb3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Rhobtb3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781722	M	MP:0000443	abnormal snout morphology	Rhobtb3<tm1a(KOMP)Wtsi>/Rhobtb3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Rhobtb3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781722	M	MP:0000438	abnormal cranium morphology	Rhobtb3<tm1a(KOMP)Wtsi>/Rhobtb3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Rhobtb3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781722	M	MP:0002100	abnormal tooth morphology	Rhobtb3<tm1a(KOMP)Wtsi>/Rhobtb3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Rhobtb3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781725	M	MP:0001262	decreased body weight	Ripk4<tm1a(EUCOMM)Wtsi>/Ripk4<+>	C57BL/6N-Ripk4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781726	F	MP:0001556	increased circulating HDL cholesterol level	Rnf10<tm1a(KOMP)Wtsi>/Rnf10<tm1a(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781726	M	MP:0000186	decreased circulating HDL cholesterol level	Rnf10<tm1a(KOMP)Wtsi>/Rnf10<tm1a(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781726	M	MP:0001262	decreased body weight	Rnf10<tm1a(KOMP)Wtsi>/Rnf10<tm1a(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781726	F	MP:0001260	increased body weight	Rnf10<tm1a(KOMP)Wtsi>/Rnf10<tm1a(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781726	M	MP:0001552	increased circulating triglyceride level	Rnf10<tm1a(KOMP)Wtsi>/Rnf10<tm1a(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781726	M	MP:0005179	decreased circulating cholesterol level	Rnf10<tm1a(KOMP)Wtsi>/Rnf10<tm1a(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781726	F	MP:0005178	increased circulating cholesterol level	Rnf10<tm1a(KOMP)Wtsi>/Rnf10<tm1a(KOMP)Wtsi>	C57BL/6N-Rnf10<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781727	M	MP:0001554	increased circulating free fatty acids level	Rpn2<tm1a(EUCOMM)Wtsi>/Rpn2<+>	B6JTyr;B6N-Rpn2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781727	M	MP:0003443	increased circulating glycerol level	Rpn2<tm1a(EUCOMM)Wtsi>/Rpn2<+>	B6JTyr;B6N-Rpn2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781727	F	MP:0003442	decreased circulating glycerol level	Rpn2<tm1a(EUCOMM)Wtsi>/Rpn2<+>	B6JTyr;B6N-Rpn2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781729	M	MP:0002942	decreased circulating alanine transaminase level	Sar1b<tm1a(EUCOMM)Wtsi>/Sar1b<+>	C57BL/6N-Sar1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781729	M	MP:0000186	decreased circulating HDL cholesterol level	Sar1b<tm1a(EUCOMM)Wtsi>/Sar1b<+>	C57BL/6N-Sar1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781729	M	MP:0001191	abnormal skin condition	Sar1b<tm1a(EUCOMM)Wtsi>/Sar1b<+>	C57BL/6N-Sar1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781729	M	MP:0005179	decreased circulating cholesterol level	Sar1b<tm1a(EUCOMM)Wtsi>/Sar1b<+>	C57BL/6N-Sar1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781729	M	MP:0000183	decreased circulating LDL cholesterol level	Sar1b<tm1a(EUCOMM)Wtsi>/Sar1b<+>	C57BL/6N-Sar1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781729	F	MP:0001554	increased circulating free fatty acids level	Sar1b<tm1a(EUCOMM)Wtsi>/Sar1b<+>	C57BL/6N-Sar1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781729	M	MP:0002702	decreased circulating free fatty acids level	Sar1b<tm1a(EUCOMM)Wtsi>/Sar1b<+>	C57BL/6N-Sar1b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781730	F	MP:0010124	decreased bone mineral content	Sdhc<tm1a(EUCOMM)Wtsi>/Sdhc<+>	C57BL/6N-Sdhc<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781730	M	MP:0010123	increased bone mineral content	Sdhc<tm1a(EUCOMM)Wtsi>/Sdhc<+>	C57BL/6N-Sdhc<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781732	M	MP:0010025	decreased total body fat amount	Sec23a<tm1a(KOMP)Wtsi>/Sec23a<+>	C57BL/6N-Sec23a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781733	M	MP:0000183	decreased circulating LDL cholesterol level	Sec24a<tm1a(KOMP)Wtsi>/Sec24a<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Sec24a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781733	M	MP:0000186	decreased circulating HDL cholesterol level	Sec24a<tm1a(KOMP)Wtsi>/Sec24a<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Sec24a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781733	M	MP:0010025	decreased total body fat amount	Sec24a<tm1a(KOMP)Wtsi>/Sec24a<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Sec24a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781733	M	MP:0005179	decreased circulating cholesterol level	Sec24a<tm1a(KOMP)Wtsi>/Sec24a<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Sec24a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781734	M	MP:0004609	vertebral fusion	Selenon<tm1a(KOMP)Wtsi>/Selenon<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Selenon<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781736	M	MP:0002966	decreased circulating alkaline phosphatase level	Setd1a<tm1a(EUCOMM)Wtsi>/Setd1a<+>	C57BL/6N-Setd1a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781736	M	MP:0003345	decreased rib number	Setd1a<tm1a(EUCOMM)Wtsi>/Setd1a<+>	C57BL/6N-Setd1a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781736	M	MP:0002942	decreased circulating alanine transaminase level	Setd1a<tm1a(EUCOMM)Wtsi>/Setd1a<+>	C57BL/6N-Setd1a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781737	F	MP:0001304	cataract	Sgo1<tm1a(EUCOMM)Wtsi>/Sgo1<+>	B6JTyr;B6N-Sgo1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781737	F	MP:0001303	abnormal lens morphology	Sgo1<tm1a(EUCOMM)Wtsi>/Sgo1<+>	B6JTyr;B6N-Sgo1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781738	M	MP:0000183	decreased circulating LDL cholesterol level	Slc16a2<tm1a(KOMP)Wtsi>/Y	B6JTyr;B6N-Slc16a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781738	M	MP:0000186	decreased circulating HDL cholesterol level	Slc16a2<tm1a(KOMP)Wtsi>/Y	B6JTyr;B6N-Slc16a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781738	M	MP:0005179	decreased circulating cholesterol level	Slc16a2<tm1a(KOMP)Wtsi>/Y	B6JTyr;B6N-Slc16a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781739	F	MP:0010088	decreased circulating fructosamine level	Slc16a2<tm1a(KOMP)Wtsi>/Slc16a2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Slc16a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781739	F	MP:0000186	decreased circulating HDL cholesterol level	Slc16a2<tm1a(KOMP)Wtsi>/Slc16a2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Slc16a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781739	F	MP:0005554	decreased circulating creatinine level	Slc16a2<tm1a(KOMP)Wtsi>/Slc16a2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Slc16a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781739	F	MP:0008806	increased circulating amylase level	Slc16a2<tm1a(KOMP)Wtsi>/Slc16a2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Slc16a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781739	F	MP:0005179	decreased circulating cholesterol level	Slc16a2<tm1a(KOMP)Wtsi>/Slc16a2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Slc16a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781739	F	MP:0002968	increased circulating alkaline phosphatase level	Slc16a2<tm1a(KOMP)Wtsi>/Slc16a2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Slc16a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781739	F	MP:0000183	decreased circulating LDL cholesterol level	Slc16a2<tm1a(KOMP)Wtsi>/Slc16a2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Slc16a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781740	M	MP:0005358	abnormal incisor morphology	Slc25a21<tm1a(KOMP)Wtsi>/Slc25a21<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Slc25a21<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781740	M	MP:0006358	absent pinna reflex	Slc25a21<tm1a(KOMP)Wtsi>/Slc25a21<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Slc25a21<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781743	M	MP:0000438	abnormal cranium morphology	Slc38a10<tm1a(EUCOMM)Wtsi>/Slc38a10<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Slc38a10<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781743	M	MP:0000455	abnormal maxilla morphology	Slc38a10<tm1a(EUCOMM)Wtsi>/Slc38a10<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Slc38a10<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781744	F	MP:0001513	limb grasping	Slc41a3<tm1a(KOMP)Wtsi>/Slc41a3<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Slc41a3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781746	M	MP:0002098	abnormal vibrissa morphology	Slc52a3<tm2a(KOMP)Wtsi>/Slc52a3<+>	B6JTyr;B6N-Slc52a3<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781746	M	MP:0001260	increased body weight	Slc52a3<tm2a(KOMP)Wtsi>/Slc52a3<+>	B6JTyr;B6N-Slc52a3<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781749	M	MP:0006241	abnormal placement of pupils	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Slx4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781749	M	MP:0001312	abnormal cornea morphology	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Slx4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781749	M	MP:0002697	abnormal eye size	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Slx4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781749	M	MP:0002697	abnormal eye size	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Slx4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781749	M	MP:0002092	abnormal eye morphology	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Slx4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781749	M	MP:0000438	abnormal cranium morphology	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Slx4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781749	M	MP:0001293	anophthalmia	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Slx4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781749	M	MP:0003179	thrombocytopenia	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Slx4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781749	M	MP:0001262	decreased body weight	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Slx4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781749	M	MP:0001314	cornea opacity	Slx4<tm1a(EUCOMM)Wtsi>/Slx4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Slx4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781752	M	MP:0000063	decreased bone mineral density	Sms<tm1a(EUCOMM)Wtsi>/Y	B6JTyr;B6N-Sms<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781752	M	MP:0003961	decreased lean body mass	Sms<tm1a(EUCOMM)Wtsi>/Y	B6JTyr;B6N-Sms<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781752	M	MP:0001262	decreased body weight	Sms<tm1a(EUCOMM)Wtsi>/Y	B6JTyr;B6N-Sms<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781752	M	MP:0001258	decreased body length	Sms<tm1a(EUCOMM)Wtsi>/Y	B6JTyr;B6N-Sms<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781752	M	MP:0005628	decreased circulating potassium level	Sms<tm1a(EUCOMM)Wtsi>/Y	B6JTyr;B6N-Sms<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781752	M	MP:0005565	increased blood urea nitrogen level	Sms<tm1a(EUCOMM)Wtsi>/Y	B6JTyr;B6N-Sms<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781752	M	MP:0005560	decreased circulating glucose level	Sms<tm1a(EUCOMM)Wtsi>/Y	B6JTyr;B6N-Sms<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781752	M	MP:0010124	decreased bone mineral content	Sms<tm1a(EUCOMM)Wtsi>/Y	B6JTyr;B6N-Sms<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781753	M	MP:0000182	increased circulating LDL cholesterol level	Smyd2<tm1a(KOMP)Wtsi>/Smyd2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Smyd2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781754	F	MP:0004924	abnormal behavior	Smyd4<tm1a(EUCOMM)Wtsi>/Smyd4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Smyd4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781754	M	MP:0003205	testicular atrophy	Smyd4<tm1a(EUCOMM)Wtsi>/Smyd4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Smyd4<tm1a(EUCOMM)Wtsi>/Wtsi	N	24652767
MGI:5781754	M	MP:0013600	testis degeneration	Smyd4<tm1a(EUCOMM)Wtsi>/Smyd4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Smyd4<tm1a(EUCOMM)Wtsi>/Wtsi	N	24652767
MGI:5781755	F	MP:0004924	abnormal behavior	Smyd5<tm1a(EUCOMM)Wtsi>/Smyd5<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Smyd5<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781756	M	MP:0001260	increased body weight	Snap29<tm1a(EUCOMM)Wtsi>/Snap29<+>	C57BL/6N-Snap29<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781756	M	MP:0010123	increased bone mineral content	Snap29<tm1a(EUCOMM)Wtsi>/Snap29<+>	C57BL/6N-Snap29<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781756	M	MP:0003960	increased lean body mass	Snap29<tm1a(EUCOMM)Wtsi>/Snap29<+>	C57BL/6N-Snap29<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781757	M	MP:0005296	abnormal humerus morphology	Snapc4<tm1a(KOMP)Wtsi>/Snapc4<+>	B6JTyr;B6N-Snapc4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781758	M	MP:0005567	decreased circulating total protein level	Snip1<tm1a(EUCOMM)Wtsi>/Snip1<+>	B6JTyr;B6N-Snip1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781759	M	MP:0000183	decreased circulating LDL cholesterol level	Snx5<tm1a(KOMP)Wtsi>/Snx5<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Snx5<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781759	M	MP:0002942	decreased circulating alanine transaminase level	Snx5<tm1a(KOMP)Wtsi>/Snx5<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Snx5<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781759	M	MP:0005179	decreased circulating cholesterol level	Snx5<tm1a(KOMP)Wtsi>/Snx5<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Snx5<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781759	M	MP:0000186	decreased circulating HDL cholesterol level	Snx5<tm1a(KOMP)Wtsi>/Snx5<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Snx5<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781760	F	MP:0002697	abnormal eye size	Socs7<tm1a(EUCOMM)Wtsi>/Socs7<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Socs7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781760	M	MP:0004924	abnormal behavior	Socs7<tm1a(EUCOMM)Wtsi>/Socs7<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Socs7<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781761	M	MP:0002834	decreased heart weight	Sparc<tm1a(EUCOMM)Wtsi>/Sparc<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Sparc<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781761	F	MP:0002100	abnormal tooth morphology	Sparc<tm1a(EUCOMM)Wtsi>/Sparc<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Sparc<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781761	F	MP:0000558	abnormal tibia morphology	Sparc<tm1a(EUCOMM)Wtsi>/Sparc<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Sparc<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781761	M	MP:0005296	abnormal humerus morphology	Sparc<tm1a(EUCOMM)Wtsi>/Sparc<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Sparc<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781761	M	MP:0002092	abnormal eye morphology	Sparc<tm1a(EUCOMM)Wtsi>/Sparc<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Sparc<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781761	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Sparc<tm1a(EUCOMM)Wtsi>/Sparc<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Sparc<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781762	M	MP:0004647	decreased lumbar vertebrae number	Spns2<tm1a(KOMP)Wtsi>/Spns2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Spns2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781762	F	MP:0000150	abnormal rib morphology	Spns2<tm1a(KOMP)Wtsi>/Spns2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Spns2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781762	M	MP:0001322	abnormal iris morphology	Spns2<tm1a(KOMP)Wtsi>/Spns2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Spns2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781762	F	MP:0001349	excessive tearing	Spns2<tm1a(KOMP)Wtsi>/Spns2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Spns2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781762	M	MP:0010101	increased sacral vertebrae number	Spns2<tm1a(KOMP)Wtsi>/Spns2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Spns2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781763	M	MP:0005179	decreased circulating cholesterol level	Sptbn1<tm1a(EUCOMM)Wtsi>/Sptbn1<+>	B6JTyr;B6N-Sptbn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781763	M	MP:0005567	decreased circulating total protein level	Sptbn1<tm1a(EUCOMM)Wtsi>/Sptbn1<+>	B6JTyr;B6N-Sptbn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781763	M	MP:0000186	decreased circulating HDL cholesterol level	Sptbn1<tm1a(EUCOMM)Wtsi>/Sptbn1<+>	B6JTyr;B6N-Sptbn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781763	M	MP:0002942	decreased circulating alanine transaminase level	Sptbn1<tm1a(EUCOMM)Wtsi>/Sptbn1<+>	B6JTyr;B6N-Sptbn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781763	M	MP:0005571	decreased lactate dehydrogenase level	Sptbn1<tm1a(EUCOMM)Wtsi>/Sptbn1<+>	B6JTyr;B6N-Sptbn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781763	M	MP:0001262	decreased body weight	Sptbn1<tm1a(EUCOMM)Wtsi>/Sptbn1<+>	B6JTyr;B6N-Sptbn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781763	M	MP:0000183	decreased circulating LDL cholesterol level	Sptbn1<tm1a(EUCOMM)Wtsi>/Sptbn1<+>	B6JTyr;B6N-Sptbn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781763	M	MP:0005419	decreased circulating serum albumin level	Sptbn1<tm1a(EUCOMM)Wtsi>/Sptbn1<+>	B6JTyr;B6N-Sptbn1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781764	F	MP:0004924	abnormal behavior	Sqstm1<tm1a(KOMP)Wtsi>/Sqstm1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Sqstm1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781764	M	MP:0005560	decreased circulating glucose level	Sqstm1<tm1a(KOMP)Wtsi>/Sqstm1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Sqstm1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781765	F	MP:0004924	abnormal behavior	Src<tm2a(EUCOMM)Wtsi>/Src<+>	B6JTyr;B6N-Src<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781765	M	MP:0000559	abnormal femur morphology	Src<tm2a(EUCOMM)Wtsi>/Src<+>	B6JTyr;B6N-Src<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781766	M	MP:0002075	abnormal coat/hair pigmentation	Srsf4<tm1a(EUCOMM)Wtsi>/Srsf4<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Srsf4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781767	M	MP:0002942	decreased circulating alanine transaminase level	St18<tm1a(KOMP)Wtsi>/St18<tm1a(KOMP)Wtsi>	C57BL/6N-St18<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781767	M	MP:0000183	decreased circulating LDL cholesterol level	St18<tm1a(KOMP)Wtsi>/St18<tm1a(KOMP)Wtsi>	C57BL/6N-St18<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781768	F	MP:0000208	decreased hematocrit	Stard13<tm1a(KOMP)Wtsi>/Stard13<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Stard13<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781769	M	MP:0000062	increased bone mineral density	Stard5<tm1a(KOMP)Wtsi>/Stard5<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Stard5<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781770	F	MP:0004647	decreased lumbar vertebrae number	Stx8<tm2a(EUCOMM)Wtsi>/Stx8<tm2a(EUCOMM)Wtsi>	B6JTyr;B6N-Stx8<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781770	F	MP:0010101	increased sacral vertebrae number	Stx8<tm2a(EUCOMM)Wtsi>/Stx8<tm2a(EUCOMM)Wtsi>	B6JTyr;B6N-Stx8<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781771	F	MP:0002074	abnormal hair texture	Supt7l<tm1a(EUCOMM)Wtsi>/Supt7l<+>	C57BL/6N-Supt7l<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781771	M	MP:0001262	decreased body weight	Supt7l<tm1a(EUCOMM)Wtsi>/Supt7l<+>	C57BL/6N-Supt7l<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781771	M	MP:0010025	decreased total body fat amount	Supt7l<tm1a(EUCOMM)Wtsi>/Supt7l<+>	C57BL/6N-Supt7l<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781772	F	MP:0010101	increased sacral vertebrae number	Kmt5b<tm1a(KOMP)Wtsi>/Kmt5b<+>	B6JTyr;B6N-Kmt5b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781772	F	MP:0004647	decreased lumbar vertebrae number	Kmt5b<tm1a(KOMP)Wtsi>/Kmt5b<+>	B6JTyr;B6N-Kmt5b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781773	F	MP:0001258	decreased body length	Kmt5b<tm1a(KOMP)Wtsi>/Kmt5b<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kmt5b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781773	F	MP:0001262	decreased body weight	Kmt5b<tm1a(KOMP)Wtsi>/Kmt5b<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kmt5b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781773	F	MP:0001973	increased thermal nociceptive threshold	Kmt5b<tm1a(KOMP)Wtsi>/Kmt5b<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Kmt5b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781774	F	MP:0004924	abnormal behavior	Sympk<tm1a(EUCOMM)Wtsi>/Sympk<+>	B6JTyr;B6N-Sympk<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781775	M	MP:0002874	decreased hemoglobin content	Sytl1<tm1a(KOMP)Wtsi>/Sytl1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Sytl1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781775	M	MP:0002608	increased hematocrit	Sytl1<tm1a(KOMP)Wtsi>/Sytl1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Sytl1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781776	F	MP:0001314	cornea opacity	Tcf7l1<tm1a(EUCOMM)Wtsi>/Tcf7l1<+>	B6JTyr;B6N-Tcf7l1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781777	F	MP:0005628	decreased circulating potassium level	Themis2<tm1a(KOMP)Wtsi>/Themis2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Themis2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781777	M	MP:0005627	increased circulating potassium level	Themis2<tm1a(KOMP)Wtsi>/Themis2<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Themis2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781778	F	MP:0001322	abnormal iris morphology	Tmem165<tm1e(EUCOMM)Wtsi>/Tmem165<tm1e(EUCOMM)Wtsi>	B6JTyr;B6N-Tmem165<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781778	M	MP:0002590	increased mean corpuscular volume	Tmem165<tm1e(EUCOMM)Wtsi>/Tmem165<tm1e(EUCOMM)Wtsi>	B6JTyr;B6N-Tmem165<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781779	M	MP:0001262	decreased body weight	Tmem98<tm1a(EUCOMM)Wtsi>/Tmem98<+>	C57BL/6N-Tmem98<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781782	M	MP:0001262	decreased body weight	Tpi1<tm1a(EUCOMM)Wtsi>/Tpi1<+>	B6JTyr;B6N-Tpi1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781784	F	MP:0010025	decreased total body fat amount	Trim66<tm1a(EUCOMM)Wtsi>/Trim66<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trim66<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781785	F	MP:0004924	abnormal behavior	Trmo<tm1a(EUCOMM)Wtsi>/Trmo<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Trmo<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781785	M	MP:0005343	increased circulating aspartate transaminase level	Trmo<tm1a(EUCOMM)Wtsi>/Trmo<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Trmo<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781786	F	MP:0001303	abnormal lens morphology	Trmt10a<tm1a(EUCOMM)Wtsi>/Trmt10a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trmt10a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781786	F	MP:0010101	increased sacral vertebrae number	Trmt10a<tm1a(EUCOMM)Wtsi>/Trmt10a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trmt10a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781786	F	MP:0001304	cataract	Trmt10a<tm1a(EUCOMM)Wtsi>/Trmt10a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trmt10a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781787	F	MP:0001312	abnormal cornea morphology	Trrap<tm1a(EUCOMM)Wtsi>/Trrap<+>	B6JTyr;B6N-Trrap<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781787	M	MP:0010092	increased circulating magnesium level	Trrap<tm1a(EUCOMM)Wtsi>/Trrap<+>	B6JTyr;B6N-Trrap<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781788	F	MP:0001325	abnormal retina morphology	Ttll4<tm1a(EUCOMM)Wtsi>/Ttll4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ttll4<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5781788	F	MP:0001413	abnormal response to new environment	Ttll4<tm1a(EUCOMM)Wtsi>/Ttll4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ttll4<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5781788	F	MP:0002896	abnormal bone mineralization	Ttll4<tm1a(EUCOMM)Wtsi>/Ttll4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ttll4<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5781791	F	MP:0004647	decreased lumbar vertebrae number	Usp42<tm2a(EUCOMM)Wtsi>/Usp42<tm2a(EUCOMM)Wtsi>	B6JTyr;B6N-Usp42<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781791	M	MP:0003179	thrombocytopenia	Usp42<tm2a(EUCOMM)Wtsi>/Usp42<tm2a(EUCOMM)Wtsi>	B6JTyr;B6N-Usp42<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781791	F	MP:0010101	increased sacral vertebrae number	Usp42<tm2a(EUCOMM)Wtsi>/Usp42<tm2a(EUCOMM)Wtsi>	B6JTyr;B6N-Usp42<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781791	M	MP:0001925	male infertility	Usp42<tm2a(EUCOMM)Wtsi>/Usp42<tm2a(EUCOMM)Wtsi>	B6JTyr;B6N-Usp42<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5781794	F	MP:0006358	absent pinna reflex	Wdr47<tm1a(EUCOMM)Wtsi>/Wdr47<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Wdr47<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781794	M	MP:0000183	decreased circulating LDL cholesterol level	Wdr47<tm1a(EUCOMM)Wtsi>/Wdr47<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Wdr47<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781794	M	MP:0001262	decreased body weight	Wdr47<tm1a(EUCOMM)Wtsi>/Wdr47<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Wdr47<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781794	F	MP:0001513	limb grasping	Wdr47<tm1a(EUCOMM)Wtsi>/Wdr47<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Wdr47<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781796	F	MP:0003961	decreased lean body mass	Zc3hc1<tm1a(KOMP)Wtsi>/Zc3hc1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Zc3hc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781796	F	MP:0001312	abnormal cornea morphology	Zc3hc1<tm1a(KOMP)Wtsi>/Zc3hc1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Zc3hc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781796	M	MP:0001925	male infertility	Zc3hc1<tm1a(KOMP)Wtsi>/Zc3hc1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Zc3hc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5781796	F	MP:0000443	abnormal snout morphology	Zc3hc1<tm1a(KOMP)Wtsi>/Zc3hc1<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Zc3hc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781797	M	MP:0000194	increased circulating calcium level	Zfp106<tm1a(KOMP)Wtsi>/Zfp106<+>	B6JTyr;B6N-Zfp106<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781798	M	MP:0001406	abnormal gait	Zfp106<tm1a(KOMP)Wtsi>/Zfp106<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Zfp106<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781798	M	MP:0009199	abnormal external male genitalia morphology	Zfp106<tm1a(KOMP)Wtsi>/Zfp106<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Zfp106<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781798	M	MP:0001973	increased thermal nociceptive threshold	Zfp106<tm1a(KOMP)Wtsi>/Zfp106<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Zfp106<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5781802	M	MP:0010025	decreased total body fat amount	Zmynd8<tm1a(EUCOMM)Wtsi>/Zmynd8<+>	B6JTyr;B6N-Zmynd8<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781802	M	MP:0005419	decreased circulating serum albumin level	Zmynd8<tm1a(EUCOMM)Wtsi>/Zmynd8<+>	B6JTyr;B6N-Zmynd8<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781803	M	MP:0004924	abnormal behavior	Zranb2<tm1a(EUCOMM)Wtsi>/Zranb2<+>	B6JTyr;B6N-Zranb2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5781803	M	MP:0010088	decreased circulating fructosamine level	Zranb2<tm1a(EUCOMM)Wtsi>/Zranb2<+>	B6JTyr;B6N-Zranb2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5285081
MGI:5782010	F	MP:0010052	increased grip strength	2310022B05Rik<tm1a(EUCOMM)Hmgu>/2310022B05Rik<tm1a(EUCOMM)Hmgu>	C57BL/6N-2310022B05Rik<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782010	F	MP:0000218	increased leukocyte cell number	2310022B05Rik<tm1a(EUCOMM)Hmgu>/2310022B05Rik<tm1a(EUCOMM)Hmgu>	C57BL/6N-2310022B05Rik<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782011	M	MP:0008045	decreased NK cell number	2810408A11Rik<tm1a(EUCOMM)Wtsi>/2810408A11Rik<tm1a(EUCOMM)Wtsi>	C57BL/6N-2810408A11Rik<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782011	M	MP:0002896	abnormal bone mineralization	2810408A11Rik<tm1a(EUCOMM)Wtsi>/2810408A11Rik<tm1a(EUCOMM)Wtsi>	C57BL/6N-2810408A11Rik<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782011	M	MP:0003795	abnormal bone structure	2810408A11Rik<tm1a(EUCOMM)Wtsi>/2810408A11Rik<tm1a(EUCOMM)Wtsi>	C57BL/6N-2810408A11Rik<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782011	F	MP:0008044	increased NK cell number	2810408A11Rik<tm1a(EUCOMM)Wtsi>/2810408A11Rik<tm1a(EUCOMM)Wtsi>	C57BL/6N-2810408A11Rik<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782011	F	MP:0008074	increased CD4-positive, alpha-beta T cell number	2810408A11Rik<tm1a(EUCOMM)Wtsi>/2810408A11Rik<tm1a(EUCOMM)Wtsi>	C57BL/6N-2810408A11Rik<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782012	M	MP:0002092	abnormal eye morphology	2900026A02Rik<tm1a(EUCOMM)Hmgu>/2900026A02Rik<tm1a(EUCOMM)Hmgu>	C57BL/6N-2900026A02Rik<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782012	M	MP:0001325	abnormal retina morphology	2900026A02Rik<tm1a(EUCOMM)Hmgu>/2900026A02Rik<tm1a(EUCOMM)Hmgu>	C57BL/6N-2900026A02Rik<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782013	M	MP:0002968	increased circulating alkaline phosphatase level	Abcb11<tm1a(EUCOMM)Hmgu>/Abcb11<tm1a(EUCOMM)Hmgu>	C57BL/6N-Abcb11<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782013	M	MP:0003960	increased lean body mass	Abcb11<tm1a(EUCOMM)Hmgu>/Abcb11<tm1a(EUCOMM)Hmgu>	C57BL/6N-Abcb11<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782013	M	MP:0005627	increased circulating potassium level	Abcb11<tm1a(EUCOMM)Hmgu>/Abcb11<tm1a(EUCOMM)Hmgu>	C57BL/6N-Abcb11<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782013	M	MP:0005343	increased circulating aspartate transaminase level	Abcb11<tm1a(EUCOMM)Hmgu>/Abcb11<tm1a(EUCOMM)Hmgu>	C57BL/6N-Abcb11<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782013	M	MP:0002941	increased circulating alanine transaminase level	Abcb11<tm1a(EUCOMM)Hmgu>/Abcb11<tm1a(EUCOMM)Hmgu>	C57BL/6N-Abcb11<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782013	M	MP:0001325	abnormal retina morphology	Abcb11<tm1a(EUCOMM)Hmgu>/Abcb11<tm1a(EUCOMM)Hmgu>	C57BL/6N-Abcb11<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782014	M	MP:0001304	cataract	Abcd1<tm1a(EUCOMM)Wtsi>/Y	B6JTyr;B6N-Abcd1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782014	M	MP:0001303	abnormal lens morphology	Abcd1<tm1a(EUCOMM)Wtsi>/Y	B6JTyr;B6N-Abcd1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782015	F	MP:0001258	decreased body length	Acap3<tm1a(EUCOMM)Hmgu>/Acap3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Acap3<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782016	F	MP:0005014	increased B cell number	Acp2<tm1a(EUCOMM)Wtsi>/Acp2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acp2<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782017	F	MP:0010052	increased grip strength	Acsbg2<tm1a(EUCOMM)Wtsi>/Acsbg2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acsbg2<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782018	F	MP:0003062	abnormal coping response	Afm<tm1a(KOMP)Wtsi>/Afm<tm1a(KOMP)Wtsi>	C57BL/6N-Afm<tm1a(KOMP)Wtsi>/Ics	N	MGI:4839251
MGI:5782018	F	MP:0000565	oligodactyly	Afm<tm1a(KOMP)Wtsi>/Afm<tm1a(KOMP)Wtsi>	C57BL/6N-Afm<tm1a(KOMP)Wtsi>/Ics	N	MGI:4839251
MGI:5782018	M	MP:0005564	increased hemoglobin content	Afm<tm1a(KOMP)Wtsi>/Afm<tm1a(KOMP)Wtsi>	C57BL/6N-Afm<tm1a(KOMP)Wtsi>/Ics	N	MGI:4839251
MGI:5782019	F	MP:0001486	abnormal startle reflex	Aldh2<tm1a(EUCOMM)Wtsi>/Aldh2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aldh2<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782019	F	MP:0001756	abnormal urination	Aldh2<tm1a(EUCOMM)Wtsi>/Aldh2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aldh2<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782019	F	MP:0000063	decreased bone mineral density	Aldh2<tm1a(EUCOMM)Wtsi>/Aldh2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aldh2<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782020	F	MP:0002591	decreased mean corpuscular volume	Aldh3a2<tm1a(EUCOMM)Wtsi>/Aldh3a2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aldh3a2<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782020	M	MP:0002875	decreased erythrocyte cell number	Aldh3a2<tm1a(EUCOMM)Wtsi>/Aldh3a2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aldh3a2<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782020	M	MP:0002874	decreased hemoglobin content	Aldh3a2<tm1a(EUCOMM)Wtsi>/Aldh3a2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aldh3a2<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782020	M	MP:0002590	increased mean corpuscular volume	Aldh3a2<tm1a(EUCOMM)Wtsi>/Aldh3a2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Aldh3a2<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782024	M	MP:0005316	abnormal response to tactile stimuli	Arhgef4<tm1a(KOMP)Wtsi>/Arhgef4<tm1a(KOMP)Wtsi>	C57BL/6N-Arhgef4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782024	M	MP:0002492	decreased IgE level	Arhgef4<tm1a(KOMP)Wtsi>/Arhgef4<tm1a(KOMP)Wtsi>	C57BL/6N-Arhgef4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782024	F	MP:0002968	increased circulating alkaline phosphatase level	Arhgef4<tm1a(KOMP)Wtsi>/Arhgef4<tm1a(KOMP)Wtsi>	C57BL/6N-Arhgef4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782024	F	MP:0005568	increased circulating total protein level	Arhgef4<tm1a(KOMP)Wtsi>/Arhgef4<tm1a(KOMP)Wtsi>	C57BL/6N-Arhgef4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782026	F	MP:0004357	long tibia	Ascc3<tm1a(EUCOMM)Hmgu>/Ascc3<+>	C57BL/6N-Ascc3<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782026	F	MP:0001566	increased circulating phosphate level	Ascc3<tm1a(EUCOMM)Hmgu>/Ascc3<+>	C57BL/6N-Ascc3<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782026	M	MP:0000198	decreased circulating phosphate level	Ascc3<tm1a(EUCOMM)Hmgu>/Ascc3<+>	C57BL/6N-Ascc3<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782027	M	MP:0001262	decreased body weight	Asns<tm1a(EUCOMM)Wtsi>/Asns<tm1a(EUCOMM)Wtsi>	C57BL/6N-Asns<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782028	F	MP:0005017	decreased B cell number	Asxl1<tm1a(EUCOMM)Wtsi>/Asxl1<+>	C57BL/6N-Asxl1<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782028	F	MP:0003062	abnormal coping response	Asxl1<tm1a(EUCOMM)Wtsi>/Asxl1<+>	C57BL/6N-Asxl1<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782029	F	MP:0001260	increased body weight	Atp8a1<tm1a(EUCOMM)Wtsi>/Atp8a1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Atp8a1<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782030	F	MP:0001391	abnormal tail movements	B4galnt3<tm1a(EUCOMM)Wtsi>/B4galnt3<tm1a(EUCOMM)Wtsi>	C57BL/6N-B4galnt3<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782031	M	MP:0001486	abnormal startle reflex	B9d1<tm1a(EUCOMM)Wtsi>/B9d1<+>	C57BL/6N-B9d1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782031	M	MP:0001260	increased body weight	B9d1<tm1a(EUCOMM)Wtsi>/B9d1<+>	C57BL/6N-B9d1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782032	F	MP:0002591	decreased mean corpuscular volume	Bag1<tm1a(EUCOMM)Hmgu>/Bag1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Bag1<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782034	F	MP:0000063	decreased bone mineral density	Firrm<tm1a(EUCOMM)Hmgu>/Firrm<+>	C57BL/6N-Firrm<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782034	F	MP:0002968	increased circulating alkaline phosphatase level	Firrm<tm1a(EUCOMM)Hmgu>/Firrm<+>	C57BL/6N-Firrm<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782034	F	MP:0002590	increased mean corpuscular volume	Firrm<tm1a(EUCOMM)Hmgu>/Firrm<+>	C57BL/6N-Firrm<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782036	M	MP:0000220	increased monocyte cell number	Bmp7<tm1a(EUCOMM)Hmgu>/Bmp7<+>	C57BL/6N-Bmp7<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782038	M	MP:0000062	increased bone mineral density	Babam2<tm1a(EUCOMM)Wtsi>/Babam2<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782038	M	MP:0001406	abnormal gait	Babam2<tm1a(EUCOMM)Wtsi>/Babam2<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782038	M	MP:0002896	abnormal bone mineralization	Babam2<tm1a(EUCOMM)Wtsi>/Babam2<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782039	M	MP:0008074	increased CD4-positive, alpha-beta T cell number	Btk<tm1a(EUCOMM)Hmgu>/Y	C57BL/6N-Btk<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782039	M	MP:0001262	decreased body weight	Btk<tm1a(EUCOMM)Hmgu>/Y	C57BL/6N-Btk<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782040	M	MP:0003313	abnormal locomotor activation	Cap2<tm1a(EUCOMM)Wtsi>/Cap2<+>	C57BL/6N-Cap2<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782040	F	MP:0001304	cataract	Cap2<tm1a(EUCOMM)Wtsi>/Cap2<+>	C57BL/6N-Cap2<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782043	F	MP:0001262	decreased body weight	Cc2d1b<tm1a(KOMP)Wtsi>/Cc2d1b<+>	Not Specified	N	MGI:4839251
MGI:5782043	F	MP:0000198	decreased circulating phosphate level	Cc2d1b<tm1a(KOMP)Wtsi>/Cc2d1b<+>	Not Specified	N	MGI:4839251
MGI:5782043	F	MP:0002702	decreased circulating free fatty acids level	Cc2d1b<tm1a(KOMP)Wtsi>/Cc2d1b<+>	Not Specified	N	MGI:4839251
MGI:5782044	F	MP:0010052	increased grip strength	Cd200<tm1a(KOMP)Wtsi>/Cd200<tm1a(KOMP)Wtsi>	C57BL/6N-Cd200<tm1a(KOMP)Wtsi>/H	N	MGI:4839251
MGI:5782047	M	MP:0001262	decreased body weight	Chrna9<tm2a(EUCOMM)Wtsi>/Chrna9<tm2a(EUCOMM)Wtsi>	C57BL/6N-Chrna9<tm2a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782048	M	MP:0003961	decreased lean body mass	Cisd2<tm1a(EUCOMM)Wtsi>/Cisd2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cisd2<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782048	M	MP:0002834	decreased heart weight	Cisd2<tm1a(EUCOMM)Wtsi>/Cisd2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cisd2<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782048	M	MP:0001402	decreased locomotor activity	Cisd2<tm1a(EUCOMM)Wtsi>/Cisd2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cisd2<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782048	M	MP:0008805	decreased circulating amylase level	Cisd2<tm1a(EUCOMM)Wtsi>/Cisd2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cisd2<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782048	M	MP:0002644	decreased circulating triglyceride level	Cisd2<tm1a(EUCOMM)Wtsi>/Cisd2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cisd2<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782048	M	MP:0002697	abnormal eye size	Cisd2<tm1a(EUCOMM)Wtsi>/Cisd2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cisd2<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782050	M	MP:0001260	increased body weight	Cops4<tm1a(EUCOMM)Hmgu>/Cops4<+>	C57BL/6N-Cops4<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782050	M	MP:0001402	decreased locomotor activity	Cops4<tm1a(EUCOMM)Hmgu>/Cops4<+>	C57BL/6N-Cops4<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782050	M	MP:0005564	increased hemoglobin content	Cops4<tm1a(EUCOMM)Hmgu>/Cops4<+>	C57BL/6N-Cops4<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782050	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Cops4<tm1a(EUCOMM)Hmgu>/Cops4<+>	C57BL/6N-Cops4<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782052	F	MP:0008501	increased IgG2b level	Crtc1<tm1a(EUCOMM)Wtsi>/Crtc1<+>	C57BL/6N-Crtc1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782053	F	MP:0001529	abnormal vocalization	D430041D05Rik<tm1a(EUCOMM)Hmgu>/D430041D05Rik<tm1a(EUCOMM)Hmgu>	C57BL/6N-D430041D05Rik<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782053	M	MP:0002075	abnormal coat/hair pigmentation	D430041D05Rik<tm1a(EUCOMM)Hmgu>/D430041D05Rik<tm1a(EUCOMM)Hmgu>	C57BL/6N-D430041D05Rik<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782053	F	MP:0002896	abnormal bone mineralization	D430041D05Rik<tm1a(EUCOMM)Hmgu>/D430041D05Rik<tm1a(EUCOMM)Hmgu>	C57BL/6N-D430041D05Rik<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782054	M	MP:0008045	decreased NK cell number	Ddx52<tm1a(EUCOMM)Wtsi>/Ddx52<+>	C57BL/6N-Ddx52<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782054	M	MP:0001262	decreased body weight	Ddx52<tm1a(EUCOMM)Wtsi>/Ddx52<+>	C57BL/6N-Ddx52<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782054	M	MP:0002896	abnormal bone mineralization	Ddx52<tm1a(EUCOMM)Wtsi>/Ddx52<+>	C57BL/6N-Ddx52<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782055	F	MP:0004924	abnormal behavior	Dhx40<tm1(NCOM)Cmhd>/Dhx40<tm1(NCOM)Cmhd>	C57BL/6N-Dhx40<tm1(NCOM)Cmhd>/Tcp	N	MGI:4839251
MGI:5782055	M	MP:0003795	abnormal bone structure	Dhx40<tm1(NCOM)Cmhd>/Dhx40<tm1(NCOM)Cmhd>	C57BL/6N-Dhx40<tm1(NCOM)Cmhd>/Tcp	N	MGI:4839251
MGI:5782055	M	MP:0000063	decreased bone mineral density	Dhx40<tm1(NCOM)Cmhd>/Dhx40<tm1(NCOM)Cmhd>	C57BL/6N-Dhx40<tm1(NCOM)Cmhd>/Tcp	N	MGI:4839251
MGI:5782055	M	MP:0002896	abnormal bone mineralization	Dhx40<tm1(NCOM)Cmhd>/Dhx40<tm1(NCOM)Cmhd>	C57BL/6N-Dhx40<tm1(NCOM)Cmhd>/Tcp	N	MGI:4839251
MGI:5782057	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Dnajc10<tm1a(EUCOMM)Hmgu>/Dnajc10<tm1a(EUCOMM)Hmgu>	C57BL/6N-Dnajc10<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782059	M	MP:0003961	decreased lean body mass	Dnajc19<tm1a(EUCOMM)Hmgu>/Dnajc19<tm1a(EUCOMM)Hmgu>	C57BL/6N-Dnajc19<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782059	M	MP:0001262	decreased body weight	Dnajc19<tm1a(EUCOMM)Hmgu>/Dnajc19<tm1a(EUCOMM)Hmgu>	C57BL/6N-Dnajc19<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782060	F	MP:0001556	increased circulating HDL cholesterol level	Dnase2b<tm1a(EUCOMM)Hmgu>/Dnase2b<tm1a(EUCOMM)Hmgu>	C57BL/6N-Dnase2b<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782061	M	MP:0002608	increased hematocrit	Dock10<tm1a(EUCOMM)Hmgu>/Dock10<tm1a(EUCOMM)Hmgu>	C57BL/6N-Dock10<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782061	F	MP:0002874	decreased hemoglobin content	Dock10<tm1a(EUCOMM)Hmgu>/Dock10<tm1a(EUCOMM)Hmgu>	C57BL/6N-Dock10<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782061	M	MP:0005564	increased hemoglobin content	Dock10<tm1a(EUCOMM)Hmgu>/Dock10<tm1a(EUCOMM)Hmgu>	C57BL/6N-Dock10<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782063	F	MP:0002702	decreased circulating free fatty acids level	Dpy19l3<tm1a(EUCOMM)Wtsi>/Dpy19l3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dpy19l3<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782065	F	MP:0000198	decreased circulating phosphate level	Drg2<tm1a(EUCOMM)Wtsi>/Drg2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Drg2<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782065	F	MP:0003313	abnormal locomotor activation	Drg2<tm1a(EUCOMM)Wtsi>/Drg2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Drg2<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782067	F	MP:0002591	decreased mean corpuscular volume	Eif2b5<tm1a(EUCOMM)Wtsi>/Eif2b5<+>	C57BL/6N-Eif2b5<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782069	F	MP:0003795	abnormal bone structure	Elk4<tm1a(EUCOMM)Wtsi>/Elk4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Elk4<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782069	F	MP:0001325	abnormal retina morphology	Elk4<tm1a(EUCOMM)Wtsi>/Elk4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Elk4<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782069	M	MP:0001312	abnormal cornea morphology	Elk4<tm1a(EUCOMM)Wtsi>/Elk4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Elk4<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782069	F	MP:0002968	increased circulating alkaline phosphatase level	Elk4<tm1a(EUCOMM)Wtsi>/Elk4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Elk4<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782069	F	MP:0008211	decreased mature B cell number	Elk4<tm1a(EUCOMM)Wtsi>/Elk4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Elk4<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782069	F	MP:0002896	abnormal bone mineralization	Elk4<tm1a(EUCOMM)Wtsi>/Elk4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Elk4<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782069	F	MP:0000063	decreased bone mineral density	Elk4<tm1a(EUCOMM)Wtsi>/Elk4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Elk4<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782069	M	MP:0001314	cornea opacity	Elk4<tm1a(EUCOMM)Wtsi>/Elk4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Elk4<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782069	M	MP:0001391	abnormal tail movements	Elk4<tm1a(EUCOMM)Wtsi>/Elk4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Elk4<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782070	F	MP:0003442	decreased circulating glycerol level	Elk4<tm1a(EUCOMM)Wtsi>/Elk4<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782070	M	MP:0005634	decreased circulating sodium level	Elk4<tm1a(EUCOMM)Wtsi>/Elk4<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782071	F	MP:0005564	increased hemoglobin content	Elmod1<tm1a(EUCOMM)Hmgu>/Elmod1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782071	M	MP:0002874	decreased hemoglobin content	Elmod1<tm1a(EUCOMM)Hmgu>/Elmod1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782071	F	MP:0005179	decreased circulating cholesterol level	Elmod1<tm1a(EUCOMM)Hmgu>/Elmod1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782071	F	MP:0000186	decreased circulating HDL cholesterol level	Elmod1<tm1a(EUCOMM)Hmgu>/Elmod1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782071	M	MP:0002968	increased circulating alkaline phosphatase level	Elmod1<tm1a(EUCOMM)Hmgu>/Elmod1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782071	F	MP:0000745	tremors	Elmod1<tm1a(EUCOMM)Hmgu>/Elmod1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782071	F	MP:0005560	decreased circulating glucose level	Elmod1<tm1a(EUCOMM)Hmgu>/Elmod1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Elmod1<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782072	M	MP:0002702	decreased circulating free fatty acids level	Emid1<tm1a(EUCOMM)Wtsi>/Emid1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Emid1<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782073	M	MP:0003442	decreased circulating glycerol level	Entpd1<tm1a(EUCOMM)Wtsi>/Entpd1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Entpd1<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782073	M	MP:0002092	abnormal eye morphology	Entpd1<tm1a(EUCOMM)Wtsi>/Entpd1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Entpd1<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782073	M	MP:0000745	tremors	Entpd1<tm1a(EUCOMM)Wtsi>/Entpd1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Entpd1<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782074	M	MP:0003960	increased lean body mass	Epb41l5<tm1a(EUCOMM)Hmgu>/Epb41l5<+>	C57BL/6N-Epb41l5<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782074	M	MP:0003442	decreased circulating glycerol level	Epb41l5<tm1a(EUCOMM)Hmgu>/Epb41l5<+>	C57BL/6N-Epb41l5<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782075	F	MP:0004599	abnormal vertebral arch morphology	Epc2<tm1a(EUCOMM)Wtsi>/Epc2<+>	Not Specified	N	MGI:4839251
MGI:5782077	M	MP:0001262	decreased body weight	Fabp12<tm1a(EUCOMM)Wtsi>/Fabp12<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fabp12<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782078	M	MP:0001304	cataract	Fabp3<tm1a(EUCOMM)Wtsi>/Fabp3<+>	C57BL/6N-Fabp3<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782078	M	MP:0001303	abnormal lens morphology	Fabp3<tm1a(EUCOMM)Wtsi>/Fabp3<+>	C57BL/6N-Fabp3<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782079	F	MP:0005566	decreased blood urea nitrogen level	Fam110b<tm1a(EUCOMM)Wtsi>/Fam110b<+>	C57BL/6N-Fam110b<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782079	M	MP:0005316	abnormal response to tactile stimuli	Fam110b<tm1a(EUCOMM)Wtsi>/Fam110b<+>	C57BL/6N-Fam110b<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782080	F	MP:0005179	decreased circulating cholesterol level	Fam117b<tm1a(EUCOMM)Wtsi>/Fam117b<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782080	M	MP:0002644	decreased circulating triglyceride level	Fam117b<tm1a(EUCOMM)Wtsi>/Fam117b<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782080	M	MP:0005566	decreased blood urea nitrogen level	Fam117b<tm1a(EUCOMM)Wtsi>/Fam117b<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782080	M	MP:0001325	abnormal retina morphology	Fam117b<tm1a(EUCOMM)Wtsi>/Fam117b<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782080	F	MP:0000186	decreased circulating HDL cholesterol level	Fam117b<tm1a(EUCOMM)Wtsi>/Fam117b<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782081	M	MP:0001262	decreased body weight	Retreg3<tm2a(EUCOMM)Wtsi>/Retreg3<tm2a(EUCOMM)Wtsi>	C57BL/6N-Retreg3<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782081	M	MP:0002874	decreased hemoglobin content	Retreg3<tm2a(EUCOMM)Wtsi>/Retreg3<tm2a(EUCOMM)Wtsi>	C57BL/6N-Retreg3<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782082	M	MP:0000183	decreased circulating LDL cholesterol level	Fam234b<tm1a(EUCOMM)Wtsi>/Fam234b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fam234b<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782082	M	MP:0005179	decreased circulating cholesterol level	Fam234b<tm1a(EUCOMM)Wtsi>/Fam234b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fam234b<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782084	F	MP:0005316	abnormal response to tactile stimuli	Fgf11<tm1a(EUCOMM)Wtsi>/Fgf11<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fgf11<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782084	M	MP:0001486	abnormal startle reflex	Fgf11<tm1a(EUCOMM)Wtsi>/Fgf11<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fgf11<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782084	F	MP:0002590	increased mean corpuscular volume	Fgf11<tm1a(EUCOMM)Wtsi>/Fgf11<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fgf11<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782085	M	MP:0002896	abnormal bone mineralization	Fgl1<tm1a(EUCOMM)Hmgu>/Fgl1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Fgl1<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782085	M	MP:0003795	abnormal bone structure	Fgl1<tm1a(EUCOMM)Hmgu>/Fgl1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Fgl1<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782086	M	MP:0001262	decreased body weight	Fhl1<tm1a(EUCOMM)Wtsi>/Fhl1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fhl1<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782086	M	MP:0005179	decreased circulating cholesterol level	Fhl1<tm1a(EUCOMM)Wtsi>/Fhl1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fhl1<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782086	M	MP:0002968	increased circulating alkaline phosphatase level	Fhl1<tm1a(EUCOMM)Wtsi>/Fhl1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fhl1<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782087	F	MP:0002874	decreased hemoglobin content	Fkbp10<tm2a(EUCOMM)Wtsi>/Fkbp10<+>	C57BL/6N-Fkbp10<tm2a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782087	M	MP:0005564	increased hemoglobin content	Fkbp10<tm2a(EUCOMM)Wtsi>/Fkbp10<+>	C57BL/6N-Fkbp10<tm2a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782087	M	MP:0002591	decreased mean corpuscular volume	Fkbp10<tm2a(EUCOMM)Wtsi>/Fkbp10<+>	C57BL/6N-Fkbp10<tm2a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782089	M	MP:0001262	decreased body weight	Fpgs<tm1a(EUCOMM)Hmgu>/Fpgs<+>	C57BL/6N-Fpgs<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782091	F	MP:0001260	increased body weight	Gap43<tm1a(EUCOMM)Wtsi>/Gap43<+>	B6JTyr;B6N-Gap43<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782091	M	MP:0001262	decreased body weight	Gap43<tm1a(EUCOMM)Wtsi>/Gap43<+>	B6JTyr;B6N-Gap43<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782092	M	MP:0003019	increased circulating chloride level	Gar1<tm1a(EUCOMM)Wtsi>/Gar1<+>	C57BL/6N-Gar1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782092	M	MP:0005633	increased circulating sodium level	Gar1<tm1a(EUCOMM)Wtsi>/Gar1<+>	C57BL/6N-Gar1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782092	F	MP:0005634	decreased circulating sodium level	Gar1<tm1a(EUCOMM)Wtsi>/Gar1<+>	C57BL/6N-Gar1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782092	F	MP:0003020	decreased circulating chloride level	Gar1<tm1a(EUCOMM)Wtsi>/Gar1<+>	C57BL/6N-Gar1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782093	F	MP:0001413	abnormal response to new environment	Gm5134<tm1a(EUCOMM)Hmgu>/Gm5134<tm1a(EUCOMM)Hmgu>	C57BL/6N-Gm5134<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782094	F	MP:0001303	abnormal lens morphology	Gmnn<tm1a(KOMP)Wtsi>/Gmnn<+>	B6JTyr;B6N-Gmnn<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782094	F	MP:0001304	cataract	Gmnn<tm1a(KOMP)Wtsi>/Gmnn<+>	B6JTyr;B6N-Gmnn<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782096	M	MP:0003313	abnormal locomotor activation	Grhl3<tm1a(EUCOMM)Wtsi>/Grhl3<+>	C57BL/6N-Grhl3<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782096	F	MP:0002092	abnormal eye morphology	Grhl3<tm1a(EUCOMM)Wtsi>/Grhl3<+>	C57BL/6N-Grhl3<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782096	F	MP:0001325	abnormal retina morphology	Grhl3<tm1a(EUCOMM)Wtsi>/Grhl3<+>	C57BL/6N-Grhl3<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782096	M	MP:0005559	increased circulating glucose level	Grhl3<tm1a(EUCOMM)Wtsi>/Grhl3<+>	C57BL/6N-Grhl3<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782096	F	MP:0002492	decreased IgE level	Grhl3<tm1a(EUCOMM)Wtsi>/Grhl3<+>	C57BL/6N-Grhl3<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782097	M	MP:0005419	decreased circulating serum albumin level	Gse1<tm1a(EUCOMM)Wtsi>/Gse1<+>	C57BL/6N-Gse1<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782097	F	MP:0005568	increased circulating total protein level	Gse1<tm1a(EUCOMM)Wtsi>/Gse1<+>	C57BL/6N-Gse1<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782097	M	MP:0005567	decreased circulating total protein level	Gse1<tm1a(EUCOMM)Wtsi>/Gse1<+>	C57BL/6N-Gse1<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782097	F	MP:0002968	increased circulating alkaline phosphatase level	Gse1<tm1a(EUCOMM)Wtsi>/Gse1<+>	C57BL/6N-Gse1<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782098	F	MP:0001406	abnormal gait	Gsk3a<tm1a(EUCOMM)Hmgu>/Gsk3a<+>	Not Specified	N	MGI:4839251
MGI:5782099	M	MP:0001406	abnormal gait	Gsk3a<tm1a(EUCOMM)Hmgu>/Gsk3a<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5782103	M	MP:0005179	decreased circulating cholesterol level	Hells<tm1a(EUCOMM)Wtsi>/Hells<tm1a(EUCOMM)Wtsi>	C57BL/6N-Hells<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782103	M	MP:0001262	decreased body weight	Hells<tm1a(EUCOMM)Wtsi>/Hells<tm1a(EUCOMM)Wtsi>	C57BL/6N-Hells<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782103	F	MP:0001406	abnormal gait	Hells<tm1a(EUCOMM)Wtsi>/Hells<tm1a(EUCOMM)Wtsi>	C57BL/6N-Hells<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782103	M	MP:0000183	decreased circulating LDL cholesterol level	Hells<tm1a(EUCOMM)Wtsi>/Hells<tm1a(EUCOMM)Wtsi>	C57BL/6N-Hells<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782103	M	MP:0000334	decreased granulocyte number	Hells<tm1a(EUCOMM)Wtsi>/Hells<tm1a(EUCOMM)Wtsi>	C57BL/6N-Hells<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782103	M	MP:0002644	decreased circulating triglyceride level	Hells<tm1a(EUCOMM)Wtsi>/Hells<tm1a(EUCOMM)Wtsi>	C57BL/6N-Hells<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782104	F	MP:0003062	abnormal coping response	Hgs<tm1a(EUCOMM)Wtsi>/Hgs<+>	Not Specified	N	MGI:4839251
MGI:5782106	M	MP:0001406	abnormal gait	Hprt1<tm1a(EUCOMM)Hmgu>/Y	C57BL/6N-Hprt1<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782107	F	MP:0002875	decreased erythrocyte cell number	Hprt1<tm1a(EUCOMM)Hmgu>/Hprt1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Hprt1<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782107	F	MP:0002874	decreased hemoglobin content	Hprt1<tm1a(EUCOMM)Hmgu>/Hprt1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Hprt1<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782108	M	MP:0003179	thrombocytopenia	Hsf2bp<tm1a(EUCOMM)Hmgu>/Hsf2bp<+>	C57BL/6N-Hsf2bp<tm1a(EUCOMM)Hmgu>/Cnrm	N	MGI:4839251
MGI:5782109	M	MP:0001260	increased body weight	Hsf2bp<tm1a(EUCOMM)Hmgu>/Hsf2bp<tm1a(EUCOMM)Hmgu>	C57BL/6N-Hsf2bp<tm1a(EUCOMM)Hmgu>/Cnrm	N	MGI:4839251
MGI:5782109	F	MP:0001756	abnormal urination	Hsf2bp<tm1a(EUCOMM)Hmgu>/Hsf2bp<tm1a(EUCOMM)Hmgu>	C57BL/6N-Hsf2bp<tm1a(EUCOMM)Hmgu>/Cnrm	N	MGI:4839251
MGI:5782109	M	MP:0001556	increased circulating HDL cholesterol level	Hsf2bp<tm1a(EUCOMM)Hmgu>/Hsf2bp<tm1a(EUCOMM)Hmgu>	C57BL/6N-Hsf2bp<tm1a(EUCOMM)Hmgu>/Cnrm	N	MGI:4839251
MGI:5782109	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Hsf2bp<tm1a(EUCOMM)Hmgu>/Hsf2bp<tm1a(EUCOMM)Hmgu>	C57BL/6N-Hsf2bp<tm1a(EUCOMM)Hmgu>/Cnrm	N	MGI:4839251
MGI:5782109	F	MP:0005560	decreased circulating glucose level	Hsf2bp<tm1a(EUCOMM)Hmgu>/Hsf2bp<tm1a(EUCOMM)Hmgu>	C57BL/6N-Hsf2bp<tm1a(EUCOMM)Hmgu>/Cnrm	N	MGI:4839251
MGI:5782109	M	MP:0005559	increased circulating glucose level	Hsf2bp<tm1a(EUCOMM)Hmgu>/Hsf2bp<tm1a(EUCOMM)Hmgu>	C57BL/6N-Hsf2bp<tm1a(EUCOMM)Hmgu>/Cnrm	N	MGI:4839251
MGI:5782112	F	MP:0001262	decreased body weight	Ikbkb<tm1a(EUCOMM)Wtsi>/Ikbkb<+>	B6JTyr;B6N-Ikbkb<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782112	M	MP:0001260	increased body weight	Ikbkb<tm1a(EUCOMM)Wtsi>/Ikbkb<+>	B6JTyr;B6N-Ikbkb<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782113	M	MP:0001260	increased body weight	Bpnt2<tm1a(KOMP)Wtsi>/Bpnt2<+>	Not Specified	N	MGI:4839251
MGI:5782114	F	MP:0003313	abnormal locomotor activation	Ino80e<tm1a(EUCOMM)Wtsi>/Ino80e<+>	C57BL/6N-Ino80e<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782115	F	MP:0002590	increased mean corpuscular volume	Itch<tm1(NCOM)Cmhd>/Itch<+>	C57BL/6N-Itch<tm1(NCOM)Cmhd>/Tcp	N	MGI:4839251
MGI:5782116	M	MP:0002092	abnormal eye morphology	Itgb5<tm1a(EUCOMM)Wtsi>/Itgb5<tm1a(EUCOMM)Wtsi>	C57BL/6N-Itgb5<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782116	M	MP:0001325	abnormal retina morphology	Itgb5<tm1a(EUCOMM)Wtsi>/Itgb5<tm1a(EUCOMM)Wtsi>	C57BL/6N-Itgb5<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782116	M	MP:0002608	increased hematocrit	Itgb5<tm1a(EUCOMM)Wtsi>/Itgb5<tm1a(EUCOMM)Wtsi>	C57BL/6N-Itgb5<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782117	M	MP:0002965	increased circulating serum albumin level	Kdm4c<tm1a(KOMP)Wtsi>/Kdm4c<+>	C57BL/6N-Kdm4c<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782117	M	MP:0000194	increased circulating calcium level	Kdm4c<tm1a(KOMP)Wtsi>/Kdm4c<+>	C57BL/6N-Kdm4c<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782117	M	MP:0005014	increased B cell number	Kdm4c<tm1a(KOMP)Wtsi>/Kdm4c<+>	C57BL/6N-Kdm4c<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782118	F	MP:0000652	enlarged sebaceous gland	Kdm4c<tm1a(KOMP)Wtsi>/Kdm4c<tm1a(KOMP)Wtsi>	C57BL/6N-Kdm4c<tm1a(KOMP)Wtsi>/Wtsi	N	25340873
MGI:5782118	M	MP:0001262	decreased body weight	Kdm4c<tm1a(KOMP)Wtsi>/Kdm4c<tm1a(KOMP)Wtsi>	C57BL/6N-Kdm4c<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782119	M	MP:0005102	abnormal iris pigmentation	Kdm8<tm1a(EUCOMM)Wtsi>/Kdm8<+>	C57BL/6N-Kdm8<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782119	F	MP:0005316	abnormal response to tactile stimuli	Kdm8<tm1a(EUCOMM)Wtsi>/Kdm8<+>	C57BL/6N-Kdm8<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782119	M	MP:0002078	abnormal glucose homeostasis	Kdm8<tm1a(EUCOMM)Wtsi>/Kdm8<+>	C57BL/6N-Kdm8<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782120	M	MP:0000745	tremors	Klhdc2<tm1a(EUCOMM)Hmgu>/Klhdc2<+>	C57BL/6N-Klhdc2<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782120	M	MP:0001314	cornea opacity	Klhdc2<tm1a(EUCOMM)Hmgu>/Klhdc2<+>	C57BL/6N-Klhdc2<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782122	F	MP:0003313	abnormal locomotor activation	Limk2<tm1a(EUCOMM)Wtsi>/Limk2<+>	C57BL/6N-Limk2<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782123	M	MP:0002608	increased hematocrit	Mapre3<tm1a(EUCOMM)Wtsi>/Mapre3<+>	C57BL/6N-Mapre3<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782125	M	MP:0001391	abnormal tail movements	Marchf9<tm1a(EUCOMM)Wtsi>/Marchf9<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782127	F	MP:0001391	abnormal tail movements	Cgas<tm1a(EUCOMM)Hmgu>/Cgas<tm1a(EUCOMM)Hmgu>	C57BL/6N-Cgas<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782129	M	MP:0001566	increased circulating phosphate level	Mcf2l<tm1a(EUCOMM)Hmgu>/Mcf2l<tm1a(EUCOMM)Hmgu>	C57BL/6N-Mcf2l<tm1a(EUCOMM)Hmgu>/Cnrm	N	MGI:4839251
MGI:5782130	M	MP:0002942	decreased circulating alanine transaminase level	Mcm10<tm1(NCOM)Cmhd>/Mcm10<+>	C57BL/6N-Mcm10<tm1(NCOM)Cmhd>/Tcp	N	MGI:4839251
MGI:5782131	F	MP:0003062	abnormal coping response	Med18<tm1a(EUCOMM)Wtsi>/Med18<+>	C57BL/6N-Med18<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782132	M	MP:0002092	abnormal eye morphology	Mib2<tm1a(EUCOMM)Wtsi>/Mib2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mib2<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782132	M	MP:0001325	abnormal retina morphology	Mib2<tm1a(EUCOMM)Wtsi>/Mib2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mib2<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782132	F	MP:0009142	decreased prepulse inhibition	Mib2<tm1a(EUCOMM)Wtsi>/Mib2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mib2<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782132	M	MP:0008805	decreased circulating amylase level	Mib2<tm1a(EUCOMM)Wtsi>/Mib2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mib2<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782134	M	MP:0003795	abnormal bone structure	Mrps35<tm1a(EUCOMM)Wtsi>/Mrps35<+>	C57BL/6N-Mrps35<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782134	M	MP:0002896	abnormal bone mineralization	Mrps35<tm1a(EUCOMM)Wtsi>/Mrps35<+>	C57BL/6N-Mrps35<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782136	M	MP:0001413	abnormal response to new environment	Mybpc3<tm1a(EUCOMM)Hmgu>/Mybpc3<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5782137	M	MP:0001399	hyperactivity	Myl4<tm1a(EUCOMM)Wtsi>/Myl4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Myl4<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782137	M	MP:0004924	abnormal behavior	Myl4<tm1a(EUCOMM)Wtsi>/Myl4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Myl4<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782139	F	MP:0010100	increased cervical vertebrae number	Myoz1<tm1a(EUCOMM)Hmgu>/Myoz1<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5782139	F	MP:0004651	increased thoracic vertebrae number	Myoz1<tm1a(EUCOMM)Hmgu>/Myoz1<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5782139	M	MP:0001262	decreased body weight	Myoz1<tm1a(EUCOMM)Hmgu>/Myoz1<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5782140	M	MP:0005634	decreased circulating sodium level	Ndufa8<tm1a(EUCOMM)Hmgu>/Ndufa8<+>	C57BL/6N-Ndufa8<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782142	F	MP:0001391	abnormal tail movements	Ndufs3<tm1a(EUCOMM)Wtsi>/Ndufs3<+>	C57BL/6N-Ndufs3<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782144	M	MP:0002702	decreased circulating free fatty acids level	Nfkbid<tm1a(EUCOMM)Wtsi>/Nfkbid<+>	C57BL/6N-Nfkbid<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782144	M	MP:0002644	decreased circulating triglyceride level	Nfkbid<tm1a(EUCOMM)Wtsi>/Nfkbid<+>	C57BL/6N-Nfkbid<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782147	M	MP:0002590	increased mean corpuscular volume	Nmnat1<tm1a(EUCOMM)Wtsi>/Nmnat1<+>	C57BL/6N-Nmnat1<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782151	F	MP:0005179	decreased circulating cholesterol level	Otud7b<tm1(NCOM)Cmhd>/Otud7b<tm1(NCOM)Cmhd>	C57BL/6N-Otud7b<tm1(NCOM)Cmhd>/Tcp	N	MGI:4839251
MGI:5782153	M	MP:0002590	increased mean corpuscular volume	Pa2g4<tm1a(EUCOMM)Wtsi>/Pa2g4<+>	Not Specified	N	MGI:4839251
MGI:5782154	F	MP:0002764	short tibia	Pacs2<tm1a(EUCOMM)Hmgu>/Pacs2<tm1a(EUCOMM)Hmgu>	C57BL/6N-Pacs2<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782156	F	MP:0000063	decreased bone mineral density	Parvb<tm1a(EUCOMM)Wtsi>/Parvb<tm1a(EUCOMM)Wtsi>	C57BL/6N-Parvb<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782156	M	MP:0000062	increased bone mineral density	Parvb<tm1a(EUCOMM)Wtsi>/Parvb<tm1a(EUCOMM)Wtsi>	C57BL/6N-Parvb<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782156	M	MP:0005567	decreased circulating total protein level	Parvb<tm1a(EUCOMM)Wtsi>/Parvb<tm1a(EUCOMM)Wtsi>	C57BL/6N-Parvb<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782156	M	MP:0008045	decreased NK cell number	Parvb<tm1a(EUCOMM)Wtsi>/Parvb<tm1a(EUCOMM)Wtsi>	C57BL/6N-Parvb<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782156	M	MP:0005560	decreased circulating glucose level	Parvb<tm1a(EUCOMM)Wtsi>/Parvb<tm1a(EUCOMM)Wtsi>	C57BL/6N-Parvb<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782156	M	MP:0005179	decreased circulating cholesterol level	Parvb<tm1a(EUCOMM)Wtsi>/Parvb<tm1a(EUCOMM)Wtsi>	C57BL/6N-Parvb<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782156	M	MP:0001260	increased body weight	Parvb<tm1a(EUCOMM)Wtsi>/Parvb<tm1a(EUCOMM)Wtsi>	C57BL/6N-Parvb<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782156	F	MP:0001262	decreased body weight	Parvb<tm1a(EUCOMM)Wtsi>/Parvb<tm1a(EUCOMM)Wtsi>	C57BL/6N-Parvb<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782157	F	MP:0001413	abnormal response to new environment	Pbx3<tm1a(EUCOMM)Wtsi>/Pbx3<+>	Not Specified	N	MGI:4839251
MGI:5782158	M	MP:0005178	increased circulating cholesterol level	Pbx3<tm1a(EUCOMM)Wtsi>/Pbx3<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782158	F	MP:0005179	decreased circulating cholesterol level	Pbx3<tm1a(EUCOMM)Wtsi>/Pbx3<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782158	M	MP:0003960	increased lean body mass	Pbx3<tm1a(EUCOMM)Wtsi>/Pbx3<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782158	F	MP:0000063	decreased bone mineral density	Pbx3<tm1a(EUCOMM)Wtsi>/Pbx3<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782158	M	MP:0000062	increased bone mineral density	Pbx3<tm1a(EUCOMM)Wtsi>/Pbx3<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782159	F	MP:0002075	abnormal coat/hair pigmentation	Per2<tm1a(EUCOMM)Hmgu>/Per2<tm1a(EUCOMM)Hmgu>	C57BL/6N-Per2<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782160	M	MP:0002896	abnormal bone mineralization	Pgd<tm1a(EUCOMM)Wtsi>/Pgd<+>	C57BL/6N-Pgd<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782161	M	MP:0001325	abnormal retina morphology	Phykpl<tm1a(EUCOMM)Wtsi>/Phykpl<tm1a(EUCOMM)Wtsi>	C57BL/6N-Phykpl<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782161	F	MP:0002966	decreased circulating alkaline phosphatase level	Phykpl<tm1a(EUCOMM)Wtsi>/Phykpl<tm1a(EUCOMM)Wtsi>	C57BL/6N-Phykpl<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782162	M	MP:0005632	decreased circulating aspartate transaminase level	Pik3c3<tm1a(EUCOMM)Wtsi>/Pik3c3<+>	C57BL/6N-Pik3c3<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782163	F	MP:0001260	increased body weight	Pla2g10<tm1a(EUCOMM)Hmgu>/Pla2g10<+>	C57BL/6N-Pla2g10<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782164	F	MP:0005633	increased circulating sodium level	Pla2g4f<tm1a(EUCOMM)Hmgu>/Pla2g4f<tm1a(EUCOMM)Hmgu>	C57BL/6N-Pla2g4f<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782165	F	MP:0001260	increased body weight	Plxnb2<tm1a(EUCOMM)Wtsi>/Plxnb2<+>	C57BL/6N-Plxnb2<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782165	F	MP:0001756	abnormal urination	Plxnb2<tm1a(EUCOMM)Wtsi>/Plxnb2<+>	C57BL/6N-Plxnb2<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782166	F	MP:0005298	abnormal clavicle morphology	Pnpt1<tm1a(KOMP)Wtsi>/Pnpt1<+>	B6JTyr;B6N-Pnpt1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782166	M	MP:0005561	increased mean corpuscular hemoglobin	Pnpt1<tm1a(KOMP)Wtsi>/Pnpt1<+>	B6JTyr;B6N-Pnpt1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782166	M	MP:0002590	increased mean corpuscular volume	Pnpt1<tm1a(KOMP)Wtsi>/Pnpt1<+>	B6JTyr;B6N-Pnpt1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782166	M	MP:0000150	abnormal rib morphology	Pnpt1<tm1a(KOMP)Wtsi>/Pnpt1<+>	B6JTyr;B6N-Pnpt1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782171	F	MP:0010052	increased grip strength	Ric1<tm1a(EUCOMM)Hmgu>/Ric1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Ric1<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782171	M	MP:0001262	decreased body weight	Ric1<tm1a(EUCOMM)Hmgu>/Ric1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Ric1<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782171	M	MP:0005017	decreased B cell number	Ric1<tm1a(EUCOMM)Hmgu>/Ric1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Ric1<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782171	M	MP:0008211	decreased mature B cell number	Ric1<tm1a(EUCOMM)Hmgu>/Ric1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Ric1<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782174	M	MP:0000220	increased monocyte cell number	Rnf169<tm1a(EUCOMM)Hmgu>/Rnf169<tm1a(EUCOMM)Hmgu>	B6NTac;B6N-Rnf169<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782174	F	MP:0002896	abnormal bone mineralization	Rnf169<tm1a(EUCOMM)Hmgu>/Rnf169<tm1a(EUCOMM)Hmgu>	B6NTac;B6N-Rnf169<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782175	M	MP:0001402	decreased locomotor activity	Rpe65<tm1a(EUCOMM)Hmgu>/Rpe65<tm1a(EUCOMM)Hmgu>	C57BL/6N-Rpe65<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782175	M	MP:0001325	abnormal retina morphology	Rpe65<tm1a(EUCOMM)Hmgu>/Rpe65<tm1a(EUCOMM)Hmgu>	C57BL/6N-Rpe65<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782175	M	MP:0001317	abnormal pupil morphology	Rpe65<tm1a(EUCOMM)Hmgu>/Rpe65<tm1a(EUCOMM)Hmgu>	C57BL/6N-Rpe65<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782175	F	MP:0000221	decreased leukocyte cell number	Rpe65<tm1a(EUCOMM)Hmgu>/Rpe65<tm1a(EUCOMM)Hmgu>	C57BL/6N-Rpe65<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782175	M	MP:0001513	limb grasping	Rpe65<tm1a(EUCOMM)Hmgu>/Rpe65<tm1a(EUCOMM)Hmgu>	C57BL/6N-Rpe65<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782175	F	MP:0001399	hyperactivity	Rpe65<tm1a(EUCOMM)Hmgu>/Rpe65<tm1a(EUCOMM)Hmgu>	C57BL/6N-Rpe65<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782175	M	MP:0000218	increased leukocyte cell number	Rpe65<tm1a(EUCOMM)Hmgu>/Rpe65<tm1a(EUCOMM)Hmgu>	C57BL/6N-Rpe65<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782176	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Rprd1b<tm1a(EUCOMM)Hmgu>/Rprd1b<+>	C57BL/6N-Rprd1b<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782178	F	MP:0004924	abnormal behavior	Rxfp2<tm1a(EUCOMM)Wtsi>/Rxfp2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782178	M	MP:0001402	decreased locomotor activity	Rxfp2<tm1a(EUCOMM)Wtsi>/Rxfp2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782178	F	MP:0000220	increased monocyte cell number	Rxfp2<tm1a(EUCOMM)Wtsi>/Rxfp2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Rxfp2<tm1a(EUCOMM)Wtsi>/Ieg	N	MGI:4839251
MGI:5782179	F	MP:0005018	decreased T cell number	Sema5b<tm1a(EUCOMM)Wtsi>/Sema5b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sema5b<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782180	M	MP:0002965	increased circulating serum albumin level	Senp3<tm1(NCOM)Cmhd>/Senp3<+>	C57BL/6N-Senp3<tm1(NCOM)Cmhd>/Tcp	N	MGI:4839251
MGI:5782181	M	MP:0003313	abnormal locomotor activation	Septin8<tm1a(EUCOMM)Wtsi>/Septin8<tm1a(EUCOMM)Wtsi>	C57BL/6N-Septin8<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782183	M	MP:0003179	thrombocytopenia	Setdb2<tm1a(KOMP)Wtsi>/Setdb2<tm1a(KOMP)Wtsi>	C57BL/6N-Setdb2<tm1a(KOMP)Wtsi>/Ieg	N	MGI:4839251
MGI:5782183	M	MP:0001406	abnormal gait	Setdb2<tm1a(KOMP)Wtsi>/Setdb2<tm1a(KOMP)Wtsi>	C57BL/6N-Setdb2<tm1a(KOMP)Wtsi>/Ieg	N	MGI:4839251
MGI:5782184	M	MP:0000745	tremors	Setmar<tm1a(EUCOMM)Wtsi>/Setmar<tm1a(EUCOMM)Wtsi>	C57BL/6N-Setmar<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782184	M	MP:0001262	decreased body weight	Setmar<tm1a(EUCOMM)Wtsi>/Setmar<tm1a(EUCOMM)Wtsi>	C57BL/6N-Setmar<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782184	M	MP:0009141	increased prepulse inhibition	Setmar<tm1a(EUCOMM)Wtsi>/Setmar<tm1a(EUCOMM)Wtsi>	C57BL/6N-Setmar<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782185	F	MP:0000745	tremors	Sgf29<tm1a(EUCOMM)Hmgu>/Sgf29<+>	C57BL/6N-Sgf29<tm1a(EUCOMM)Hmgu>/Cnrm	N	MGI:4839251
MGI:5782186	M	MP:0000062	increased bone mineral density	Sirt2<tm1a(EUCOMM)Wtsi>/Sirt2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sirt2<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782186	F	MP:0005178	increased circulating cholesterol level	Sirt2<tm1a(EUCOMM)Wtsi>/Sirt2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sirt2<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782189	M	MP:0009199	abnormal external male genitalia morphology	Slc22a21<tm1a(KOMP)Wtsi>/Slc22a21<tm1a(KOMP)Wtsi>	B6JTyr;B6N-Slc22a21<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782191	M	MP:0002644	decreased circulating triglyceride level	Slc35f6<tm1a(EUCOMM)Wtsi>/Slc35f6<tm1a(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782192	F	MP:0001552	increased circulating triglyceride level	Slc38a10<tm2a(EUCOMM)Wtsi>/Slc38a10<tm2a(EUCOMM)Wtsi>	C57BL/6N-Slc38a10<tm2a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782192	M	MP:0002092	abnormal eye morphology	Slc38a10<tm2a(EUCOMM)Wtsi>/Slc38a10<tm2a(EUCOMM)Wtsi>	C57BL/6N-Slc38a10<tm2a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782192	M	MP:0001325	abnormal retina morphology	Slc38a10<tm2a(EUCOMM)Wtsi>/Slc38a10<tm2a(EUCOMM)Wtsi>	C57BL/6N-Slc38a10<tm2a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782192	F	MP:0005627	increased circulating potassium level	Slc38a10<tm2a(EUCOMM)Wtsi>/Slc38a10<tm2a(EUCOMM)Wtsi>	C57BL/6N-Slc38a10<tm2a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782192	M	MP:0005316	abnormal response to tactile stimuli	Slc38a10<tm2a(EUCOMM)Wtsi>/Slc38a10<tm2a(EUCOMM)Wtsi>	C57BL/6N-Slc38a10<tm2a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782194	M	MP:0002075	abnormal coat/hair pigmentation	Smoc1<tm1a(EUCOMM)Wtsi>/Smoc1<+>	C57BL/6N-Smoc1<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782196	F	MP:0006241	abnormal placement of pupils	Snip1<tm1a(EUCOMM)Wtsi>/Snip1<+>	Not Specified	N	MGI:4839251
MGI:5782200	F	MP:0005553	increased circulating creatinine level	Srsf4<tm1a(EUCOMM)Wtsi>/Srsf4<+>	C57BL/6N-Srsf4<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782205	F	MP:0000550	abnormal forelimb morphology	Tcf7<tm1a(EUCOMM)Wtsi>/Tcf7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tcf7<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782205	M	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Tcf7<tm1a(EUCOMM)Wtsi>/Tcf7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tcf7<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782205	F	MP:0005316	abnormal response to tactile stimuli	Tcf7<tm1a(EUCOMM)Wtsi>/Tcf7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tcf7<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782205	M	MP:0005014	increased B cell number	Tcf7<tm1a(EUCOMM)Wtsi>/Tcf7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tcf7<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782205	M	MP:0001304	cataract	Tcf7<tm1a(EUCOMM)Wtsi>/Tcf7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tcf7<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782205	F	MP:0000564	syndactyly	Tcf7<tm1a(EUCOMM)Wtsi>/Tcf7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tcf7<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782205	M	MP:0005018	decreased T cell number	Tcf7<tm1a(EUCOMM)Wtsi>/Tcf7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tcf7<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782205	M	MP:0002968	increased circulating alkaline phosphatase level	Tcf7<tm1a(EUCOMM)Wtsi>/Tcf7<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tcf7<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782206	F	MP:0000745	tremors	Thrb<tm2a(EUCOMM)Wtsi>/Thrb<tm2a(EUCOMM)Wtsi>	C57BL/6N-Thrb<tm2a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782206	M	MP:0003442	decreased circulating glycerol level	Thrb<tm2a(EUCOMM)Wtsi>/Thrb<tm2a(EUCOMM)Wtsi>	C57BL/6N-Thrb<tm2a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782207	M	MP:0005567	decreased circulating total protein level	Tmem167<tm1a(EUCOMM)Hmgu>/Tmem167<+>	C57BL/6N-Tmem167<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782207	M	MP:0002644	decreased circulating triglyceride level	Tmem167<tm1a(EUCOMM)Hmgu>/Tmem167<+>	C57BL/6N-Tmem167<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782207	F	MP:0002965	increased circulating serum albumin level	Tmem167<tm1a(EUCOMM)Hmgu>/Tmem167<+>	C57BL/6N-Tmem167<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782207	M	MP:0005419	decreased circulating serum albumin level	Tmem167<tm1a(EUCOMM)Hmgu>/Tmem167<+>	C57BL/6N-Tmem167<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782208	M	MP:0000745	tremors	Tmem255b<tm1a(EUCOMM)Hmgu>/Tmem255b<tm1a(EUCOMM)Hmgu>	C57BL/6N-Tmem255b<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782209	M	MP:0000194	increased circulating calcium level	Tmem68<tm1a(EUCOMM)Wtsi>/Tmem68<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tmem68<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782209	F	MP:0005628	decreased circulating potassium level	Tmem68<tm1a(EUCOMM)Wtsi>/Tmem68<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tmem68<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782210	M	MP:0001262	decreased body weight	Tmem94<tm1a(EUCOMM)Wtsi>/Tmem94<+>	C57BL/6N-Tmem94<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782211	M	MP:0001552	increased circulating triglyceride level	Tnfaip1<tm1a(EUCOMM)Wtsi>/Tnfaip1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tnfaip1<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782211	M	MP:0000063	decreased bone mineral density	Tnfaip1<tm1a(EUCOMM)Wtsi>/Tnfaip1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tnfaip1<tm1a(EUCOMM)Wtsi>/H	N	MGI:4839251
MGI:5782212	M	MP:0010053	decreased grip strength	Tnfrsf1b<tm1a(EUCOMM)Wtsi>/Tnfrsf1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tnfrsf1b<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782212	F	MP:0001402	decreased locomotor activity	Tnfrsf1b<tm1a(EUCOMM)Wtsi>/Tnfrsf1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tnfrsf1b<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782212	F	MP:0005018	decreased T cell number	Tnfrsf1b<tm1a(EUCOMM)Wtsi>/Tnfrsf1b<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tnfrsf1b<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782213	M	MP:0010025	decreased total body fat amount	Trafd1<tm1a(EUCOMM)Wtsi>/Trafd1<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Trafd1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782215	M	MP:0005505	thrombocytosis	Ttc39b<tm1e(EUCOMM)Wtsi>/Ttc39b<tm1e(EUCOMM)Wtsi>	Not Specified	N	MGI:4839251
MGI:5782216	F	MP:0001391	abnormal tail movements	Ttll1<tm1a(EUCOMM)Wtsi>/Ttll1<+>	C57BL/6N-Ttll1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782217	F	MP:0005628	decreased circulating potassium level	Ttll3<tm1a(EUCOMM)Wtsi>/Ttll3<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Ttll3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782218	M	MP:0001262	decreased body weight	Twf1<tm1a(EUCOMM)Wtsi>/Twf1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Twf1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782218	M	MP:0001191	abnormal skin condition	Twf1<tm1a(EUCOMM)Wtsi>/Twf1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Twf1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782219	F	MP:0001552	increased circulating triglyceride level	Ube2b<tm1a(EUCOMM)Wtsi>/Ube2b<+>	C57BL/6N-Ube2b<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782219	F	MP:0004924	abnormal behavior	Ube2b<tm1a(EUCOMM)Wtsi>/Ube2b<+>	C57BL/6N-Ube2b<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782219	M	MP:0002644	decreased circulating triglyceride level	Ube2b<tm1a(EUCOMM)Wtsi>/Ube2b<+>	C57BL/6N-Ube2b<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782220	M	MP:0001406	abnormal gait	Uhrf1<tm1a(EUCOMM)Wtsi>/Uhrf1<+>	Not Specified	N	MGI:4839251
MGI:5782221	M	MP:0000565	oligodactyly	Usp12<tm1a(EUCOMM)Hmgu>/Usp12<+>	Not Specified	N	MGI:4839251
MGI:5782222	F	MP:0002833	increased heart weight	Usp12<tm1a(EUCOMM)Hmgu>/Usp12<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5782222	M	MP:0001262	decreased body weight	Usp12<tm1a(EUCOMM)Hmgu>/Usp12<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5782222	M	MP:0002834	decreased heart weight	Usp12<tm1a(EUCOMM)Hmgu>/Usp12<tm1a(EUCOMM)Hmgu>	Not Specified	N	MGI:4839251
MGI:5782226	F	MP:0005018	decreased T cell number	Wrnip1<tm1a(EUCOMM)Wtsi>/Wrnip1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Wrnip1<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782226	M	MP:0005316	abnormal response to tactile stimuli	Wrnip1<tm1a(EUCOMM)Wtsi>/Wrnip1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Wrnip1<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782226	M	MP:0002644	decreased circulating triglyceride level	Wrnip1<tm1a(EUCOMM)Wtsi>/Wrnip1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Wrnip1<tm1a(EUCOMM)Wtsi>/Cnrm	N	MGI:4839251
MGI:5782227	M	MP:0005018	decreased T cell number	Xbp1<tm1a(EUCOMM)Wtsi>/Xbp1<+>	C57BL/6N-Xbp1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782227	M	MP:0008495	decreased IgG1 level	Xbp1<tm1a(EUCOMM)Wtsi>/Xbp1<+>	C57BL/6N-Xbp1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782227	M	MP:0005179	decreased circulating cholesterol level	Xbp1<tm1a(EUCOMM)Wtsi>/Xbp1<+>	C57BL/6N-Xbp1<tm1a(EUCOMM)Wtsi>/Ics	N	MGI:4839251
MGI:5782228	F	MP:0001391	abnormal tail movements	Yipf1<tm1a(EUCOMM)Wtsi>/Yipf1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Yipf1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:4839251
MGI:5782229	M	MP:0000063	decreased bone mineral density	Zbtb45<tm1(NCOM)Cmhd>/Zbtb45<tm1(NCOM)Cmhd>	C57BL/6N-Zbtb45<tm1(NCOM)Cmhd>/Tcp	N	MGI:4839251
MGI:5782230	M	MP:0002874	decreased hemoglobin content	Zfp13<tm1a(EUCOMM)Hmgu>/Zfp13<tm1a(EUCOMM)Hmgu>	C57BL/6N-Zfp13<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:4839251
MGI:5782232	F	MP:0003062	abnormal coping response	Zfp715<tm1a(EUCOMM)Hmgu>/Zfp715<tm1a(EUCOMM)Hmgu>	C57BL/6N-Zfp715<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782232	M	MP:0005179	decreased circulating cholesterol level	Zfp715<tm1a(EUCOMM)Hmgu>/Zfp715<tm1a(EUCOMM)Hmgu>	C57BL/6N-Zfp715<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782232	F	MP:0005178	increased circulating cholesterol level	Zfp715<tm1a(EUCOMM)Hmgu>/Zfp715<tm1a(EUCOMM)Hmgu>	C57BL/6N-Zfp715<tm1a(EUCOMM)Hmgu>/H	N	MGI:4839251
MGI:5782233	M	MP:0002608	increased hematocrit	Zfp760<tm1a(EUCOMM)Hmgu>/Zfp760<+>	C57BL/6N-Zfp760<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782233	M	MP:0001262	decreased body weight	Zfp760<tm1a(EUCOMM)Hmgu>/Zfp760<+>	C57BL/6N-Zfp760<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782233	M	MP:0003131	increased erythrocyte cell number	Zfp760<tm1a(EUCOMM)Hmgu>/Zfp760<+>	C57BL/6N-Zfp760<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782233	M	MP:0003179	thrombocytopenia	Zfp760<tm1a(EUCOMM)Hmgu>/Zfp760<+>	C57BL/6N-Zfp760<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:4839251
MGI:5782316	M	MP:0003960	increased lean body mass	Cimip2c<tm1a(EUCOMM)Wtsi>/Cimip2c<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cimip2c<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782317	M	MP:0005567	decreased circulating total protein level	Cracdl<tm1b(KOMP)Wtsi>/Cracdl<tm1b(KOMP)Wtsi>	C57BL/6N-Cracdl<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782317	M	MP:0000195	decreased circulating calcium level	Cracdl<tm1b(KOMP)Wtsi>/Cracdl<tm1b(KOMP)Wtsi>	C57BL/6N-Cracdl<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782317	M	MP:0000186	decreased circulating HDL cholesterol level	Cracdl<tm1b(KOMP)Wtsi>/Cracdl<tm1b(KOMP)Wtsi>	C57BL/6N-Cracdl<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782317	M	MP:0005179	decreased circulating cholesterol level	Cracdl<tm1b(KOMP)Wtsi>/Cracdl<tm1b(KOMP)Wtsi>	C57BL/6N-Cracdl<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782317	M	MP:0005419	decreased circulating serum albumin level	Cracdl<tm1b(KOMP)Wtsi>/Cracdl<tm1b(KOMP)Wtsi>	C57BL/6N-Cracdl<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782331	M	MP:0000208	decreased hematocrit	Dmgdh<tm1a(KOMP)Wtsi>/Dmgdh<tm1a(KOMP)Wtsi>	C57BL/6N-Dmgdh<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782332	M	MP:0002941	increased circulating alanine transaminase level	Eci3<tm1b(EUCOMM)Wtsi>/Eci3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eci3<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782340	M	MP:0002941	increased circulating alanine transaminase level	Il23r<tm2a(EUCOMM)Wtsi>/Il23r<tm2a(EUCOMM)Wtsi>	C57BL/6N-Il23r<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782342	M	MP:0010087	increased circulating fructosamine level	Irak1<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Irak1<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:5782352	M	MP:0004609	vertebral fusion	Lyplal1<tm1a(KOMP)Wtsi>/Lyplal1<tm1a(KOMP)Wtsi>	C57BL/6N-Lyplal1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782352	F	MP:0002968	increased circulating alkaline phosphatase level	Lyplal1<tm1a(KOMP)Wtsi>/Lyplal1<tm1a(KOMP)Wtsi>	C57BL/6N-Lyplal1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782359	M	MP:0002599	increased mean platelet volume	Polb<tm1a(KOMP)Wtsi>/Polb<+>	C57BL/6N-Polb<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782359	M	MP:0010025	decreased total body fat amount	Polb<tm1a(KOMP)Wtsi>/Polb<+>	C57BL/6N-Polb<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782359	M	MP:0003960	increased lean body mass	Polb<tm1a(KOMP)Wtsi>/Polb<+>	C57BL/6N-Polb<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782364	M	MP:0000186	decreased circulating HDL cholesterol level	Rpia<tm1a(KOMP)Wtsi>/Rpia<+>	C57BL/6N-Rpia<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782364	M	MP:0000195	decreased circulating calcium level	Rpia<tm1a(KOMP)Wtsi>/Rpia<+>	C57BL/6N-Rpia<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782364	M	MP:0003442	decreased circulating glycerol level	Rpia<tm1a(KOMP)Wtsi>/Rpia<+>	C57BL/6N-Rpia<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782366	M	MP:0002833	increased heart weight	Sec1<tm1a(EUCOMM)Wtsi>/Sec1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sec1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782368	M	MP:0000221	decreased leukocyte cell number	Uevld<tm1a(EUCOMM)Wtsi>/Uevld<tm1a(EUCOMM)Wtsi>	C57BL/6N-Uevld<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782372	M	MP:0010024	increased total body fat amount	Ypel4<tm1a(EUCOMM)Wtsi>/Ypel4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ypel4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782372	M	MP:0001554	increased circulating free fatty acids level	Ypel4<tm1a(EUCOMM)Wtsi>/Ypel4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ypel4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782373	F	MP:0010052	increased grip strength	Zfp84<tm1b(KOMP)Wtsi>/Zfp84<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp84<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782373	M	MP:0005179	decreased circulating cholesterol level	Zfp84<tm1b(KOMP)Wtsi>/Zfp84<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp84<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5782373	M	MP:0000186	decreased circulating HDL cholesterol level	Zfp84<tm1b(KOMP)Wtsi>/Zfp84<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp84<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5784489	F	MP:0001131	abnormal ovarian follicle morphology	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	26061565
MGI:5784489	F	MP:0005182	increased circulating estradiol level	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	26061565
MGI:5784489	F	MP:0012411	increased granulosa cell tumor incidence	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	26061565
MGI:5784489	F	MP:0002016	ovary cyst	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	26061565
MGI:5784489	F	MP:0005418	abnormal circulating hormone level	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	26061565
MGI:5784489	F	MP:0002773	decreased circulating luteinizing hormone level	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	26061565
MGI:5784489	F	MP:0001749	suppressed circulating follicle stimulating hormone level	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S6/SvEvTac * 129S7/SvEvBrd	N	26061565
MGI:5784494	F	MP:0001749	suppressed circulating follicle stimulating hormone level	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Tg(CYP19A1-cre)1Jri/0	involves: 129S6/SvEvTac	N	26061565
MGI:5784494	F	MP:0008868	abnormal granulosa cell morphology	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Tg(CYP19A1-cre)1Jri/0	involves: 129S6/SvEvTac	N	26061565
MGI:5784494	F	MP:0012411	increased granulosa cell tumor incidence	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Tg(CYP19A1-cre)1Jri/0	involves: 129S6/SvEvTac	N	26061565
MGI:5784494	F	MP:0005182	increased circulating estradiol level	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Tg(CYP19A1-cre)1Jri/0	involves: 129S6/SvEvTac	N	26061565
MGI:5784494	F	MP:0001131	abnormal ovarian follicle morphology	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Tg(CYP19A1-cre)1Jri/0	involves: 129S6/SvEvTac	N	26061565
MGI:5784494	F	MP:0005418	abnormal circulating hormone level	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Tg(CYP19A1-cre)1Jri/0	involves: 129S6/SvEvTac	N	26061565
MGI:5784494	F	MP:0002773	decreased circulating luteinizing hormone level	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Tg(CYP19A1-cre)1Jri/0	involves: 129S6/SvEvTac	N	26061565
MGI:5784501	F	MP:0001749	suppressed circulating follicle stimulating hormone level	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129S6/SvEvTac	N	26061565
MGI:5784501	F	MP:0005418	abnormal circulating hormone level	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129S6/SvEvTac	N	26061565
MGI:5784501	F	MP:0002773	decreased circulating luteinizing hormone level	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129S6/SvEvTac	N	26061565
MGI:5784501	F	MP:0012411	increased granulosa cell tumor incidence	Foxo1<tm1Rdp>/Foxo1<tm1.1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1.1Rdp>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CYP19A1-cre)1Jri/0	involves: 129S4/SvJae * 129S6/SvEvTac	N	26061565
MGI:5784667	M	MP:0011431	increased urine flow rate	Nlrp6<tm1Opaz>/Nlrp6<tm1Opaz>	B6.Cg-Nlrp6<tm1Opaz>	N	20923861
MGI:5784667	F	MP:0012306	enhanced spatial learning	Nlrp6<tm1Opaz>/Nlrp6<tm1Opaz>	B6.Cg-Nlrp6<tm1Opaz>	N	20923861
MGI:5784667	M	MP:0012307	impaired spatial learning	Nlrp6<tm1Opaz>/Nlrp6<tm1Opaz>	B6.Cg-Nlrp6<tm1Opaz>	N	20923861
MGI:5784667	F	MP:0001364	decreased anxiety-related response	Nlrp6<tm1Opaz>/Nlrp6<tm1Opaz>	B6.Cg-Nlrp6<tm1Opaz>	N	20923861
MGI:5784667	M	MP:0002988	decreased urine osmolality	Nlrp6<tm1Opaz>/Nlrp6<tm1Opaz>	B6.Cg-Nlrp6<tm1Opaz>	N	20923861
MGI:5784674	F	MP:0001126	abnormal ovary morphology	Gt(ROSA)26Sor<tm1(Pik3ca*H1047R)Egan>/Gt(ROSA)26Sor<+>	involves: 129S6/SvEvTac * CD-1	N	25625625
MGI:5784674	F	MP:0002006	neoplasm	Gt(ROSA)26Sor<tm1(Pik3ca*H1047R)Egan>/Gt(ROSA)26Sor<+>	involves: 129S6/SvEvTac * CD-1	Y	25625625
MGI:5784677	F	MP:0008000	increased ovary tumor incidence	Arid1a<tm1.1Mag>/Arid1a<tm1.1Mag>,Gt(ROSA)26Sor<tm1(Pik3ca*H1047R)Egan>/Gt(ROSA)26Sor<+>	involves: 129S6/SvEvTac * CD-1	N	25625625
MGI:5784677	F	MP:0008705	increased interleukin-6 secretion	Arid1a<tm1.1Mag>/Arid1a<tm1.1Mag>,Gt(ROSA)26Sor<tm1(Pik3ca*H1047R)Egan>/Gt(ROSA)26Sor<+>	involves: 129S6/SvEvTac * CD-1	N	25625625
MGI:5784677	F	MP:0013184	hemorrhagic ascites	Arid1a<tm1.1Mag>/Arid1a<tm1.1Mag>,Gt(ROSA)26Sor<tm1(Pik3ca*H1047R)Egan>/Gt(ROSA)26Sor<+>	involves: 129S6/SvEvTac * CD-1	N	25625625
MGI:5784677	F	MP:0003579	increased ovarian carcinoma incidence	Arid1a<tm1.1Mag>/Arid1a<tm1.1Mag>,Gt(ROSA)26Sor<tm1(Pik3ca*H1047R)Egan>/Gt(ROSA)26Sor<+>	involves: 129S6/SvEvTac * CD-1	N	25625625
MGI:5784677	F	MP:0001272	increased metastatic potential	Arid1a<tm1.1Mag>/Arid1a<tm1.1Mag>,Gt(ROSA)26Sor<tm1(Pik3ca*H1047R)Egan>/Gt(ROSA)26Sor<+>	involves: 129S6/SvEvTac * CD-1	N	25625625
MGI:5784679	F	MP:0001126	abnormal ovary morphology	Arid1a<tm1.1Mag>/Arid1a<+>,Gt(ROSA)26Sor<tm1(Pik3ca*H1047R)Egan>/Gt(ROSA)26Sor<+>	involves: 129S6/SvEvTac * CD-1	N	25625625
MGI:5784679	F	MP:0002006	neoplasm	Arid1a<tm1.1Mag>/Arid1a<+>,Gt(ROSA)26Sor<tm1(Pik3ca*H1047R)Egan>/Gt(ROSA)26Sor<+>	involves: 129S6/SvEvTac * CD-1	Y	25625625
MGI:5784746	F	MP:0002574	increased vertical activity	Crebrf<Gt(YHD319)Byg>/Crebrf<Gt(YHD319)Byg>	B6.129P2-Crebrf<Gt(YHD319)Byg>	N	23071095
MGI:5784746	F	MP:0001364	decreased anxiety-related response	Crebrf<Gt(YHD319)Byg>/Crebrf<Gt(YHD319)Byg>	B6.129P2-Crebrf<Gt(YHD319)Byg>	N	23071095
MGI:5784746	F	MP:0001386	abnormal maternal nurturing	Crebrf<Gt(YHD319)Byg>/Crebrf<Gt(YHD319)Byg>	B6.129P2-Crebrf<Gt(YHD319)Byg>	N	23071095
MGI:5784746	F	MP:0002665	decreased circulating corticosterone level	Crebrf<Gt(YHD319)Byg>/Crebrf<Gt(YHD319)Byg>	B6.129P2-Crebrf<Gt(YHD319)Byg>	N	23071095
MGI:5784746	F	MP:0001399	hyperactivity	Crebrf<Gt(YHD319)Byg>/Crebrf<Gt(YHD319)Byg>	B6.129P2-Crebrf<Gt(YHD319)Byg>	N	23071095
MGI:5784746	F	MP:0005121	decreased circulating prolactin level	Crebrf<Gt(YHD319)Byg>/Crebrf<Gt(YHD319)Byg>	B6.129P2-Crebrf<Gt(YHD319)Byg>	N	23071095
MGI:5784746	F	MP:0005376	homeostasis/metabolism phenotype	Crebrf<Gt(YHD319)Byg>/Crebrf<Gt(YHD319)Byg>	B6.129P2-Crebrf<Gt(YHD319)Byg>	Y	23071095
MGI:5784746	F	MP:0001360	abnormal social investigation	Crebrf<Gt(YHD319)Byg>/Crebrf<Gt(YHD319)Byg>	B6.129P2-Crebrf<Gt(YHD319)Byg>	N	23071095
MGI:5784746	F	MP:0006270	abnormal mammary gland growth during lactation	Crebrf<Gt(YHD319)Byg>/Crebrf<Gt(YHD319)Byg>	B6.129P2-Crebrf<Gt(YHD319)Byg>	N	23071095
MGI:5785065	M	MP:0005560	decreased circulating glucose level	Abca7<tm2b(EUCOMM)Hmgu>/Abca7<tm2b(EUCOMM)Hmgu>	B6N(Cg)-Abca7<tm2b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5785065	F	MP:0013279	increased fasting circulating glucose level	Abca7<tm2b(EUCOMM)Hmgu>/Abca7<tm2b(EUCOMM)Hmgu>	B6N(Cg)-Abca7<tm2b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5785071	F	MP:0003795	abnormal bone structure	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	F	MP:0000219	increased neutrophil cell number	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	M	MP:0010025	decreased total body fat amount	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	M	MP:0000432	abnormal head morphology	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	M	MP:0005560	decreased circulating glucose level	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	M	MP:0008805	decreased circulating amylase level	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	F	MP:0000063	decreased bone mineral density	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	M	MP:0005292	improved glucose tolerance	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	M	MP:0005565	increased blood urea nitrogen level	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	F	MP:0005633	increased circulating sodium level	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	M	MP:0000221	decreased leukocyte cell number	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	F	MP:0002874	decreased hemoglobin content	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	F	MP:0001340	abnormal eyelid morphology	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	F	MP:0000208	decreased hematocrit	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	M	MP:0008045	decreased NK cell number	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785071	M	MP:0008078	increased CD8-positive, alpha-beta T cell number	Duoxa2<tm1b(KOMP)Wtsi>/Duoxa2<tm1b(KOMP)Wtsi>	C57BL/6N-Duoxa2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5785072	F	MP:0002833	increased heart weight	Elk1<tm1.1(KOMP)Vlcg>/Elk1<tm1.1(KOMP)Vlcg>	C57BL/6N-Elk1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5785073	M	MP:0004151	decreased circulating iron level	Fam217b<tm1.1(KOMP)Vlcg>/Fam217b<tm1.1(KOMP)Vlcg>	C57BL/6N-Fam217b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5785073	M	MP:0011436	decreased urine magnesium level	Fam217b<tm1.1(KOMP)Vlcg>/Fam217b<tm1.1(KOMP)Vlcg>	C57BL/6N-Fam217b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5785073	M	MP:0005560	decreased circulating glucose level	Fam217b<tm1.1(KOMP)Vlcg>/Fam217b<tm1.1(KOMP)Vlcg>	C57BL/6N-Fam217b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5785075	F	MP:0005293	impaired glucose tolerance	Gdi2<tm1b(EUCOMM)Hmgu>/Gdi2<+>	C57BL/6N-Gdi2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5785075	M	MP:0001325	abnormal retina morphology	Gdi2<tm1b(EUCOMM)Hmgu>/Gdi2<+>	C57BL/6N-Gdi2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5785080	F	MP:0003019	increased circulating chloride level	Mcrs1<tm1.1(KOMP)Vlcg>/Mcrs1<+>	C57BL/6N-Mcrs1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5785087	M	MP:0002941	increased circulating alanine transaminase level	Rrp8<tm1.1(KOMP)Vlcg>/Rrp8<+>	C57BL/6N-Rrp8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5785087	F	MP:0003064	decreased coping response	Rrp8<tm1.1(KOMP)Vlcg>/Rrp8<+>	C57BL/6N-Rrp8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5785091	F	MP:0013278	decreased fasting circulating glucose level	Vegfb<tm1b(EUCOMM)Hmgu>/Vegfb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vegfb<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5785091	M	MP:0001523	impaired righting response	Vegfb<tm1b(EUCOMM)Hmgu>/Vegfb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vegfb<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5785091	M	MP:0000198	decreased circulating phosphate level	Vegfb<tm1b(EUCOMM)Hmgu>/Vegfb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vegfb<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5785091	M	MP:0003131	increased erythrocyte cell number	Vegfb<tm1b(EUCOMM)Hmgu>/Vegfb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vegfb<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5785091	M	MP:0005564	increased hemoglobin content	Vegfb<tm1b(EUCOMM)Hmgu>/Vegfb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vegfb<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5785092	M	MP:0002833	increased heart weight	Zfp961<tm1.1(KOMP)Mbp>/Zfp961<tm1.1(KOMP)Mbp>	C57BL/6N-Zfp961<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5785092	F	MP:0002968	increased circulating alkaline phosphatase level	Zfp961<tm1.1(KOMP)Mbp>/Zfp961<tm1.1(KOMP)Mbp>	C57BL/6N-Zfp961<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5787999	F	MP:0001175	abnormal lung morphology	Mfap4<tm1Ascr>/Mfap4<tm1Ascr>	B6.129S1-Mfap4<tm1Ascr>	N	26033354
MGI:5787999	F	MP:0010937	increased total lung capacity	Mfap4<tm1Ascr>/Mfap4<tm1Ascr>	B6.129S1-Mfap4<tm1Ascr>	N	26033354
MGI:5787999	F	MP:0002327	abnormal respiratory function	Mfap4<tm1Ascr>/Mfap4<tm1Ascr>	B6.129S1-Mfap4<tm1Ascr>	N	26033354
MGI:5787999	F	MP:0010895	increased lung compliance	Mfap4<tm1Ascr>/Mfap4<tm1Ascr>	B6.129S1-Mfap4<tm1Ascr>	N	26033354
MGI:5787999	F	MP:0010901	abnormal pulmonary alveolar parenchyma morphology	Mfap4<tm1Ascr>/Mfap4<tm1Ascr>	B6.129S1-Mfap4<tm1Ascr>	N	26033354
MGI:5787999	F	MP:0011045	decreased lung elastance	Mfap4<tm1Ascr>/Mfap4<tm1Ascr>	B6.129S1-Mfap4<tm1Ascr>	N	26033354
MGI:5788185	M	MP:0005389	reproductive system phenotype	Ppp3cc<tm1.1Osb>/Ppp3cc<tm1.1Osb>	involves: C57BL/6 * DBA/2	Y	26429887
MGI:5788185	M	MP:0001925	male infertility	Ppp3cc<tm1.1Osb>/Ppp3cc<tm1.1Osb>	involves: C57BL/6 * DBA/2	N	26429887
MGI:5788185	M	MP:0009831	abnormal sperm midpiece morphology	Ppp3cc<tm1.1Osb>/Ppp3cc<tm1.1Osb>	involves: C57BL/6 * DBA/2	N	26429887
MGI:5788185	M	MP:0000242	impaired fertilization	Ppp3cc<tm1.1Osb>/Ppp3cc<tm1.1Osb>	involves: C57BL/6 * DBA/2	N	26429887
MGI:5788185	M	MP:0009282	decreased hyperactivated sperm motility	Ppp3cc<tm1.1Osb>/Ppp3cc<tm1.1Osb>	involves: C57BL/6 * DBA/2	N	26429887
MGI:5788186	M	MP:0009282	decreased hyperactivated sperm motility	Ppp3r2<em1Osb>/Ppp3r2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	26429887
MGI:5788186	M	MP:0009831	abnormal sperm midpiece morphology	Ppp3r2<em1Osb>/Ppp3r2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	26429887
MGI:5788186	M	MP:0001925	male infertility	Ppp3r2<em1Osb>/Ppp3r2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	26429887
MGI:5788563	M	MP:0008195	abnormal professional antigen presenting cell morphology	Cln3<tm1Nbm>/Cln3<tm1Nbm>	involves: 129S6/SvEvTac * C57BL/6J	N	27101989
MGI:5788563	M	MP:0002376	abnormal dendritic cell physiology	Cln3<tm1Nbm>/Cln3<tm1Nbm>	involves: 129S6/SvEvTac * C57BL/6J	N	27101989
MGI:5788563	M	MP:0011079	decreased macrophage cytokine production	Cln3<tm1Nbm>/Cln3<tm1Nbm>	involves: 129S6/SvEvTac * C57BL/6J	N	27101989
MGI:5788563	M	MP:0002451	abnormal macrophage physiology	Cln3<tm1Nbm>/Cln3<tm1Nbm>	involves: 129S6/SvEvTac * C57BL/6J	N	27101989
MGI:5788563	M	MP:0003566	abnormal cell adhesion	Cln3<tm1Nbm>/Cln3<tm1Nbm>	involves: 129S6/SvEvTac * C57BL/6J	N	27101989
MGI:5788772	M	MP:0003599	large penis	Sgta<tm1.1Drmcr>/Sgta<tm1.1Drmcr>	involves: C57BL/6	N	27358191
MGI:5788772	M	MP:0003830	abnormal testis development	Sgta<tm1.1Drmcr>/Sgta<tm1.1Drmcr>	involves: C57BL/6	N	27358191
MGI:5788774	M	MP:0003599	large penis	Sgta<tm1.1Drmcr>/Sgta<+>	involves: C57BL/6	N	27358191
MGI:5788774	M	MP:0002717	abnormal male preputial gland morphology	Sgta<tm1.1Drmcr>/Sgta<+>	involves: C57BL/6	N	27358191
MGI:5788774	F	MP:0004701	decreased circulating insulin-like growth factor I level	Sgta<tm1.1Drmcr>/Sgta<+>	involves: C57BL/6	N	27358191
MGI:5789378	M	MP:0002968	increased circulating alkaline phosphatase level	Alk<tm2.1Ics>/Alk<+>	B6N.129S2(Cg)-Alk<tm2.1Ics>	N	24811761
MGI:5789378	M	MP:0003019	increased circulating chloride level	Alk<tm2.1Ics>/Alk<+>	B6N.129S2(Cg)-Alk<tm2.1Ics>	N	24811761
MGI:5789378	M	MP:0004924	abnormal behavior	Alk<tm2.1Ics>/Alk<+>	B6N.129S2(Cg)-Alk<tm2.1Ics>	N	24811761
MGI:5789378	M	MP:0011940	decreased food intake	Alk<tm2.1Ics>/Alk<+>	B6N.129S2(Cg)-Alk<tm2.1Ics>	N	24811761
MGI:5789378	M	MP:0002757	decreased vertical activity	Alk<tm2.1Ics>/Alk<+>	B6N.129S2(Cg)-Alk<tm2.1Ics>	N	24811761
MGI:5789378	M	MP:0001402	decreased locomotor activity	Alk<tm2.1Ics>/Alk<+>	B6N.129S2(Cg)-Alk<tm2.1Ics>	N	24811761
MGI:5789378	M	MP:0001363	increased anxiety-related response	Alk<tm2.1Ics>/Alk<+>	B6N.129S2(Cg)-Alk<tm2.1Ics>	N	24811761
MGI:5789378	M	MP:0002092	abnormal eye morphology	Alk<tm2.1Ics>/Alk<+>	B6N.129S2(Cg)-Alk<tm2.1Ics>	N	24811761
MGI:5789378	M	MP:0010052	increased grip strength	Alk<tm2.1Ics>/Alk<+>	B6N.129S2(Cg)-Alk<tm2.1Ics>	N	24811761
MGI:5789537	M	MP:0003064	decreased coping response	Csf1r<tm1Ers>/Csf1r<+>	B6.129X1-Csf1r<tm1Ers>	N	25497733
MGI:5789537	F	MP:0001393	ataxia	Csf1r<tm1Ers>/Csf1r<+>	B6.129X1-Csf1r<tm1Ers>	N	25497733
MGI:5789537	M	MP:0001363	increased anxiety-related response	Csf1r<tm1Ers>/Csf1r<+>	B6.129X1-Csf1r<tm1Ers>	N	25497733
MGI:5789933	M	MP:0011698	abnormal brown adipose tissue physiology	Appl1<Gt(RRS819)Byg>/Appl1<Gt(RRS819)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24813896
MGI:5789933	M	MP:0020101	abnormal hepatic glucose production	Appl1<Gt(RRS819)Byg>/Appl1<Gt(RRS819)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24813896
MGI:5789933	M	MP:0013279	increased fasting circulating glucose level	Appl1<Gt(RRS819)Byg>/Appl1<Gt(RRS819)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24813896
MGI:5789933	M	MP:0002079	increased circulating insulin level	Appl1<Gt(RRS819)Byg>/Appl1<Gt(RRS819)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24813896
MGI:5789933	M	MP:0005331	insulin resistance	Appl1<Gt(RRS819)Byg>/Appl1<Gt(RRS819)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24813896
MGI:5789933	M	MP:0011016	increased core body temperature	Appl1<Gt(RRS819)Byg>/Appl1<Gt(RRS819)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24813896
MGI:5789933	M	MP:0005376	homeostasis/metabolism phenotype	Appl1<Gt(RRS819)Byg>/Appl1<Gt(RRS819)Byg>	involves: 129P2/OlaHsd * C57BL/6	Y	24813896
MGI:5789933	M	MP:0001399	hyperactivity	Appl1<Gt(RRS819)Byg>/Appl1<Gt(RRS819)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24813896
MGI:5789933	M	MP:0005378	growth/size/body region phenotype	Appl1<Gt(RRS819)Byg>/Appl1<Gt(RRS819)Byg>	involves: 129P2/OlaHsd * C57BL/6	Y	24813896
MGI:5789933	M	MP:0005386	behavior/neurological phenotype	Appl1<Gt(RRS819)Byg>/Appl1<Gt(RRS819)Byg>	involves: 129P2/OlaHsd * C57BL/6	Y	24813896
MGI:5789933	M	MP:0005293	impaired glucose tolerance	Appl1<Gt(RRS819)Byg>/Appl1<Gt(RRS819)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	24813896
MGI:5789942	M	MP:0000351	increased cell proliferation	Ltf<tm1.2Smoc>/Ltf<tm1.2Smoc>	involves: 129 * C57BL/6J	N	25057912
MGI:5789942	M	MP:0006043	decreased apoptosis	Ltf<tm1.2Smoc>/Ltf<tm1.2Smoc>	involves: 129 * C57BL/6J	N	25057912
MGI:5789942	M	MP:0004499	increased incidence of tumors by chemical induction	Ltf<tm1.2Smoc>/Ltf<tm1.2Smoc>	involves: 129 * C57BL/6J	N	25057912
MGI:5789948	F	MP:0001126	abnormal ovary morphology	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	M	MP:0013279	increased fasting circulating glucose level	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	M	MP:0002727	decreased circulating insulin level	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	F	MP:0001926	female infertility	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	F	MP:0005431	decreased oocyte number	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	F	MP:0006283	increased medulloblastoma incidence	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	M	MP:0013600	testis degeneration	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	M	MP:0002786	abnormal Leydig cell morphology	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	F	MP:0002016	ovary cyst	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	F	MP:0002038	increased carcinoma incidence	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	M	MP:0001925	male infertility	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	F	MP:0008000	increased ovary tumor incidence	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	M	MP:0006362	abnormal male germ cell morphology	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	M	MP:0001147	small testis	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	M	MP:0001751	increased circulating luteinizing hormone level	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	M	MP:0001750	increased circulating follicle stimulating hormone level	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	F	MP:0004805	absent oocytes	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	M	MP:0001152	increased Leydig cell number	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5789948	M	MP:0011940	decreased food intake	Trim37<Gt(RRO307)Byg>/Trim37<Gt(RRO307)Byg>	B6J.129P2-Trim37<Gt(RRO307)Byg>	N	27044324
MGI:5790076	M	MP:0001405	impaired coordination	Ip6k3<tm1.1Snyd>/Ip6k3<tm1.1Snyd>	Not Specified	N	26245967
MGI:5790076	M	MP:0000890	thin cerebellar molecular layer	Ip6k3<tm1.1Snyd>/Ip6k3<tm1.1Snyd>	Not Specified	N	26245967
MGI:5790076	M	MP:0021018	decreased dendritic spine number	Ip6k3<tm1.1Snyd>/Ip6k3<tm1.1Snyd>	Not Specified	N	26245967
MGI:5790076	M	MP:0000877	abnormal Purkinje cell morphology	Ip6k3<tm1.1Snyd>/Ip6k3<tm1.1Snyd>	Not Specified	N	26245967
MGI:5790076	M	MP:0001406	abnormal gait	Ip6k3<tm1.1Snyd>/Ip6k3<tm1.1Snyd>	Not Specified	N	26245967
MGI:5790076	M	MP:0002804	abnormal motor learning	Ip6k3<tm1.1Snyd>/Ip6k3<tm1.1Snyd>	Not Specified	N	26245967
MGI:5790076	M	MP:0003631	nervous system phenotype	Ip6k3<tm1.1Snyd>/Ip6k3<tm1.1Snyd>	Not Specified	Y	26245967
MGI:5790076	M	MP:0008143	abnormal dendrite morphology	Ip6k3<tm1.1Snyd>/Ip6k3<tm1.1Snyd>	Not Specified	N	26245967
MGI:5790076	M	MP:0003633	abnormal nervous system physiology	Ip6k3<tm1.1Snyd>/Ip6k3<tm1.1Snyd>	Not Specified	N	26245967
MGI:5790076	M	MP:0004998	decreased CNS synapse formation	Ip6k3<tm1.1Snyd>/Ip6k3<tm1.1Snyd>	Not Specified	N	26245967
MGI:5790076	M	MP:0008572	abnormal Purkinje cell dendrite morphology	Ip6k3<tm1.1Snyd>/Ip6k3<tm1.1Snyd>	Not Specified	N	26245967
MGI:5790076	M	MP:0003245	abnormal GABAergic neuron morphology	Ip6k3<tm1.1Snyd>/Ip6k3<tm1.1Snyd>	Not Specified	N	26245967
MGI:5790374	M	MP:0008261	arrest of male meiosis	Brdt<tm1a(EUCOMM)Wtsi>/Brdt<tm1a(EUCOMM)Wtsi>	C57BL/6-Brdt<tm1a(EUCOMM)Wtsi>	N	26994494
MGI:5790374	M	MP:0002780	decreased circulating testosterone level	Brdt<tm1a(EUCOMM)Wtsi>/Brdt<tm1a(EUCOMM)Wtsi>	C57BL/6-Brdt<tm1a(EUCOMM)Wtsi>	N	26994494
MGI:5790374	M	MP:0002216	abnormal seminiferous tubule morphology	Brdt<tm1a(EUCOMM)Wtsi>/Brdt<tm1a(EUCOMM)Wtsi>	C57BL/6-Brdt<tm1a(EUCOMM)Wtsi>	N	26994494
MGI:5790374	M	MP:0014052	increased male germ cell apoptosis	Brdt<tm1a(EUCOMM)Wtsi>/Brdt<tm1a(EUCOMM)Wtsi>	C57BL/6-Brdt<tm1a(EUCOMM)Wtsi>	N	26994494
MGI:5790374	M	MP:0001938	delayed sexual maturation	Brdt<tm1a(EUCOMM)Wtsi>/Brdt<tm1a(EUCOMM)Wtsi>	C57BL/6-Brdt<tm1a(EUCOMM)Wtsi>	N	26994494
MGI:5790374	M	MP:0006379	abnormal spermatocyte morphology	Brdt<tm1a(EUCOMM)Wtsi>/Brdt<tm1a(EUCOMM)Wtsi>	C57BL/6-Brdt<tm1a(EUCOMM)Wtsi>	N	26994494
MGI:5790374	M	MP:0006380	abnormal spermatid morphology	Brdt<tm1a(EUCOMM)Wtsi>/Brdt<tm1a(EUCOMM)Wtsi>	C57BL/6-Brdt<tm1a(EUCOMM)Wtsi>	N	26994494
MGI:5790374	M	MP:0001925	male infertility	Brdt<tm1a(EUCOMM)Wtsi>/Brdt<tm1a(EUCOMM)Wtsi>	C57BL/6-Brdt<tm1a(EUCOMM)Wtsi>	N	26994494
MGI:5790374	M	MP:0004852	decreased testis weight	Brdt<tm1a(EUCOMM)Wtsi>/Brdt<tm1a(EUCOMM)Wtsi>	C57BL/6-Brdt<tm1a(EUCOMM)Wtsi>	N	26994494
MGI:5790374	M	MP:0005159	azoospermia	Brdt<tm1a(EUCOMM)Wtsi>/Brdt<tm1a(EUCOMM)Wtsi>	C57BL/6-Brdt<tm1a(EUCOMM)Wtsi>	N	26994494
MGI:5790374	M	MP:0013330	abnormal male accessory sex gland morphology	Brdt<tm1a(EUCOMM)Wtsi>/Brdt<tm1a(EUCOMM)Wtsi>	C57BL/6-Brdt<tm1a(EUCOMM)Wtsi>	N	26994494
MGI:5790374	M	MP:0001156	abnormal spermatogenesis	Brdt<tm1a(EUCOMM)Wtsi>/Brdt<tm1a(EUCOMM)Wtsi>	C57BL/6-Brdt<tm1a(EUCOMM)Wtsi>	N	26994494
MGI:5790399	M	MP:0006380	abnormal spermatid morphology	Necab2<tm1a(KOMP)Wtsi>/Necab2<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5790416	F	MP:0002169	no abnormal phenotype detected	Fundc1<tm1a(KOMP)Wtsi>/Fundc1<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5790417	M	MP:0002169	no abnormal phenotype detected	Fundc1<tm1a(KOMP)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5790635	M	MP:0002635	reduced sensorimotor gating	Pdgfrb<tm1Msas>/Pdgfrb<tm1Msas>,Tg(Nes-cre)1Nogu/0	B6J.Cg-Pdgfrb<tm1Msas> Tg(Nes-cre)1Nogu	N	25803852
MGI:5790635	M	MP:0008948	decreased neuron number	Pdgfrb<tm1Msas>/Pdgfrb<tm1Msas>,Tg(Nes-cre)1Nogu/0	B6J.Cg-Pdgfrb<tm1Msas> Tg(Nes-cre)1Nogu	N	25803852
MGI:5790635	M	MP:0001360	abnormal social investigation	Pdgfrb<tm1Msas>/Pdgfrb<tm1Msas>,Tg(Nes-cre)1Nogu/0	B6J.Cg-Pdgfrb<tm1Msas> Tg(Nes-cre)1Nogu	N	25803852
MGI:5790635	M	MP:0009142	decreased prepulse inhibition	Pdgfrb<tm1Msas>/Pdgfrb<tm1Msas>,Tg(Nes-cre)1Nogu/0	B6J.Cg-Pdgfrb<tm1Msas> Tg(Nes-cre)1Nogu	N	25803852
MGI:5790635	M	MP:0002272	abnormal nervous system electrophysiology	Pdgfrb<tm1Msas>/Pdgfrb<tm1Msas>,Tg(Nes-cre)1Nogu/0	B6J.Cg-Pdgfrb<tm1Msas> Tg(Nes-cre)1Nogu	N	25803852
MGI:5790646	M	MP:0009105	penis prolapse	Gnptab<nym>/Gnptab<nym>	involves: BALB/cAnNHsd * C3H/HeNHsd	N	25107912
MGI:5790831	M	MP:0002784	abnormal Sertoli cell morphology	Abhd5<tm1a(KOMP)Wtsi>/Abhd5<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5790841	F	MP:0001129	impaired ovarian folliculogenesis	Il33<tm1(KOMP)Vlcg>/Il33<tm1(KOMP)Vlcg>	C57BL/6-Il33<tm1(KOMP)Vlcg>	N	25617473
MGI:5790841	F	MP:0001131	abnormal ovarian follicle morphology	Il33<tm1(KOMP)Vlcg>/Il33<tm1(KOMP)Vlcg>	C57BL/6-Il33<tm1(KOMP)Vlcg>	N	25617473
MGI:5790841	F	MP:0001126	abnormal ovary morphology	Il33<tm1(KOMP)Vlcg>/Il33<tm1(KOMP)Vlcg>	C57BL/6-Il33<tm1(KOMP)Vlcg>	N	25617473
MGI:5790841	F	MP:0003799	impaired macrophage chemotaxis	Il33<tm1(KOMP)Vlcg>/Il33<tm1(KOMP)Vlcg>	C57BL/6-Il33<tm1(KOMP)Vlcg>	N	25617473
MGI:5790841	F	MP:0008260	abnormal autophagy	Il33<tm1(KOMP)Vlcg>/Il33<tm1(KOMP)Vlcg>	C57BL/6-Il33<tm1(KOMP)Vlcg>	N	25617473
MGI:5790841	F	MP:0002680	decreased corpora lutea number	Il33<tm1(KOMP)Vlcg>/Il33<tm1(KOMP)Vlcg>	C57BL/6-Il33<tm1(KOMP)Vlcg>	N	25617473
MGI:5790841	F	MP:0003507	abnormal ovary physiology	Il33<tm1(KOMP)Vlcg>/Il33<tm1(KOMP)Vlcg>	C57BL/6-Il33<tm1(KOMP)Vlcg>	N	25617473
MGI:5790841	F	MP:0031420	decreased superovulation rate	Il33<tm1(KOMP)Vlcg>/Il33<tm1(KOMP)Vlcg>	C57BL/6-Il33<tm1(KOMP)Vlcg>	N	25617473
MGI:5790841	F	MP:0008995	early reproductive senescence	Il33<tm1(KOMP)Vlcg>/Il33<tm1(KOMP)Vlcg>	C57BL/6-Il33<tm1(KOMP)Vlcg>	N	25617473
MGI:5790953	M	MP:0013600	testis degeneration	Socs7<tm1a(EUCOMM)Wtsi>/Socs7<tm1a(EUCOMM)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791066	M	MP:0010124	decreased bone mineral content	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791066	M	MP:0002687	oligozoospermia	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791066	M	MP:0001922	reduced male fertility	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791066	M	MP:0004174	abnormal spine curvature	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791066	M	MP:0013600	testis degeneration	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791066	M	MP:0001262	decreased body weight	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791066	M	MP:0003961	decreased lean body mass	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791066	M	MP:0000063	decreased bone mineral density	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791066	M	MP:0008039	increased NK T cell number	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791066	M	MP:0002161	abnormal fertility/fecundity	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791066	M	MP:0000162	lordosis	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791066	M	MP:0008044	increased NK cell number	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791066	M	MP:0001258	decreased body length	Sms<tm1a(EUCOMM)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791071	F	MP:0001258	decreased body length	Tpd52l2<tm1a(KOMP)Wtsi>/Tpd52l2<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791071	F	MP:0000609	abnormal liver physiology	Tpd52l2<tm1a(KOMP)Wtsi>/Tpd52l2<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24652767
MGI:5791913	M	MP:0001489	decreased startle reflex	Mir34a<tm1.2Arte>/Mir34a<tm1.2Arte>	involves: C57BL/6N	N	25348795
MGI:5791913	F	MP:0005574	decreased pulmonary respiratory rate	Mir34a<tm1.2Arte>/Mir34a<tm1.2Arte>	involves: C57BL/6N	N	25348795
MGI:5791913	M	MP:0005014	increased B cell number	Mir34a<tm1.2Arte>/Mir34a<tm1.2Arte>	involves: C57BL/6N	N	25348795
MGI:5791913	F	MP:0005576	decreased pulmonary ventilation	Mir34a<tm1.2Arte>/Mir34a<tm1.2Arte>	involves: C57BL/6N	N	25348795
MGI:5791926	F	MP:0000627	abnormal mammary gland morphology	Tg(MMTVTGFA)257Rjc/0	involves: C57BL/6 * DBA/2	N	2161707
MGI:5792142	M	MP:0005386	behavior/neurological phenotype	Hdac6<tm1Anfi>/Hdac6<tm1Anfi>	Not Specified	Y	23184605
MGI:5792142	M	MP:0008414	abnormal spatial reference memory	Hdac6<tm1Anfi>/Hdac6<tm1Anfi>	Not Specified	N	23184605
MGI:5792142	M	MP:0005384	cellular phenotype	Hdac6<tm1Anfi>/Hdac6<tm1Anfi>	Not Specified	Y	23184605
MGI:5792142	M	MP:0003631	nervous system phenotype	Hdac6<tm1Anfi>/Hdac6<tm1Anfi>	Not Specified	Y	23184605
MGI:5792693	M	MP:0001406	abnormal gait	Ptchd1<tm2.2Gfng>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27007844
MGI:5792693	M	MP:0014114	abnormal cognition	Ptchd1<tm2.2Gfng>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27007844
MGI:5792693	M	MP:0012312	impaired avoidance learning behavior	Ptchd1<tm2.2Gfng>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27007844
MGI:5792693	M	MP:0004144	hypotonia	Ptchd1<tm2.2Gfng>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27007844
MGI:5792693	M	MP:0005386	behavior/neurological phenotype	Ptchd1<tm2.2Gfng>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	27007844
MGI:5792693	M	MP:0009456	impaired cued conditioning behavior	Ptchd1<tm2.2Gfng>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27007844
MGI:5792693	M	MP:0001399	hyperactivity	Ptchd1<tm2.2Gfng>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27007844
MGI:5792693	M	MP:0009454	impaired contextual conditioning behavior	Ptchd1<tm2.2Gfng>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27007844
MGI:5792693	M	MP:0005655	increased aggression	Ptchd1<tm2.2Gfng>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27007844
MGI:5792693	M	MP:0003463	abnormal single cell response	Ptchd1<tm2.2Gfng>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27007844
MGI:5792693	M	MP:0001501	abnormal sleep pattern	Ptchd1<tm2.2Gfng>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27007844
MGI:5792693	M	MP:0003631	nervous system phenotype	Ptchd1<tm2.2Gfng>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	27007844
MGI:5792694	M	MP:0005386	behavior/neurological phenotype	Ptchd1<tm2.1Gfng>/Y,Sst<tm2.1(cre)Zjh>/Sst<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	Y	27007844
MGI:5792694	M	MP:0001399	hyperactivity	Ptchd1<tm2.1Gfng>/Y,Sst<tm2.1(cre)Zjh>/Sst<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	27007844
MGI:5792694	M	MP:0014114	abnormal cognition	Ptchd1<tm2.1Gfng>/Y,Sst<tm2.1(cre)Zjh>/Sst<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	27007844
MGI:5792694	M	MP:0009436	fragmentation of sleep/wake states	Ptchd1<tm2.1Gfng>/Y,Sst<tm2.1(cre)Zjh>/Sst<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	N	27007844
MGI:5792824	M	MP:0013601	increased testis apoptosis	Knstrn<tm1d(KOMP)Wtsi>/Knstrn<tm1d(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26667018
MGI:5792824	M	MP:0002687	oligozoospermia	Knstrn<tm1d(KOMP)Wtsi>/Knstrn<tm1d(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26667018
MGI:5792824	M	MP:0004852	decreased testis weight	Knstrn<tm1d(KOMP)Wtsi>/Knstrn<tm1d(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26667018
MGI:5792824	M	MP:0004901	decreased male germ cell number	Knstrn<tm1d(KOMP)Wtsi>/Knstrn<tm1d(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26667018
MGI:5792824	M	MP:0002685	abnormal spermatogonia proliferation	Knstrn<tm1d(KOMP)Wtsi>/Knstrn<tm1d(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26667018
MGI:5792824	M	MP:0002784	abnormal Sertoli cell morphology	Knstrn<tm1d(KOMP)Wtsi>/Knstrn<tm1d(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26667018
MGI:5792824	M	MP:0001156	abnormal spermatogenesis	Knstrn<tm1d(KOMP)Wtsi>/Knstrn<tm1d(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26667018
MGI:5792824	M	MP:0001147	small testis	Knstrn<tm1d(KOMP)Wtsi>/Knstrn<tm1d(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26667018
MGI:5792824	F	MP:0005389	reproductive system phenotype	Knstrn<tm1d(KOMP)Wtsi>/Knstrn<tm1d(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	Y	26667018
MGI:5792824	M	MP:0002216	abnormal seminiferous tubule morphology	Knstrn<tm1d(KOMP)Wtsi>/Knstrn<tm1d(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26667018
MGI:5792902	M	MP:0008808	decreased spleen iron level	Hjv<tm1Kpan>/Hjv<tm1Kpan>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6	N	21748766
MGI:5792902	M	MP:0005638	hemochromatosis	Hjv<tm1Kpan>/Hjv<tm1Kpan>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6	N	21748766
MGI:5792902	M	MP:0005637	abnormal iron homeostasis	Hjv<tm1Kpan>/Hjv<tm1Kpan>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6	N	21748766
MGI:5792902	M	MP:0008807	increased liver iron level	Hjv<tm1Kpan>/Hjv<tm1Kpan>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6	N	21748766
MGI:5792902	M	MP:0011897	decreased circulating unsaturated transferrin level	Hjv<tm1Kpan>/Hjv<tm1Kpan>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6	N	21748766
MGI:5792902	M	MP:0008810	increased circulating iron level	Hjv<tm1Kpan>/Hjv<tm1Kpan>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6	N	21748766
MGI:5792902	M	MP:0011890	increased circulating ferritin level	Hjv<tm1Kpan>/Hjv<tm1Kpan>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6	N	21748766
MGI:5792902	M	MP:0002446	abnormal macrophage morphology	Hjv<tm1Kpan>/Hjv<tm1Kpan>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129S6/SvEvTac * C57BL/6	N	21748766
MGI:5792903	M	MP:0002169	no abnormal phenotype detected	Hjv<tm1Kpan>/Hjv<tm1Kpan>,Tg(Ckmm-cre)5Khn/0	involves: 129S6/SvEvTac * C57BL/6 * FVB	N	21748766
MGI:5792904	M	MP:0008807	increased liver iron level	Hjv<tm1Nca>/Hjv<tm1Nca>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	21748766
MGI:5792904	M	MP:0005637	abnormal iron homeostasis	Hjv<tm1Nca>/Hjv<tm1Nca>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	N	21748766
MGI:5792957	M	MP:0003331	increased hepatocellular carcinoma incidence	Tg(Alb1-Myc)#Sst/0,Tg(MtTGFA)Lmb/0	involves: C57BL/6 * CBA * CD-1	N	21771728
MGI:5792957	M	MP:0008039	increased NK T cell number	Tg(Alb1-Myc)#Sst/0,Tg(MtTGFA)Lmb/0	involves: C57BL/6 * CBA * CD-1	N	21771728
MGI:5792957	M	MP:0008045	decreased NK cell number	Tg(Alb1-Myc)#Sst/0,Tg(MtTGFA)Lmb/0	involves: C57BL/6 * CBA * CD-1	N	21771728
MGI:5793075	M	MP:0010836	decreased CD4-positive, alpha-beta memory T cell number	Irf5<tm1e(EUCOMM)Wtsi>/Irf5<tm1e(EUCOMM)Wtsi>	C57BL/6N-Irf5<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5793075	M	MP:0000221	decreased leukocyte cell number	Irf5<tm1e(EUCOMM)Wtsi>/Irf5<tm1e(EUCOMM)Wtsi>	C57BL/6N-Irf5<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5793076	M	MP:0010067	increased red blood cell distribution width	Klf14<tm1.1(KOMP)Vlcg>/Klf14<tm1.1(KOMP)Vlcg>	C57BL/6N-Klf14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5793076	M	MP:0002574	increased vertical activity	Klf14<tm1.1(KOMP)Vlcg>/Klf14<tm1.1(KOMP)Vlcg>	C57BL/6N-Klf14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5793076	F	MP:0005562	decreased mean corpuscular hemoglobin	Klf14<tm1.1(KOMP)Vlcg>/Klf14<tm1.1(KOMP)Vlcg>	C57BL/6N-Klf14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5793076	F	MP:0002941	increased circulating alanine transaminase level	Klf14<tm1.1(KOMP)Vlcg>/Klf14<tm1.1(KOMP)Vlcg>	C57BL/6N-Klf14<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5795669	M	MP:0009420	skeletal muscle endomysial fibrosis	Dmd<mdx>/Y,Utrn<tm1Jrs>/Utrn<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	17889902
MGI:5795669	M	MP:0013467	diaphragmitis	Dmd<mdx>/Y,Utrn<tm1Jrs>/Utrn<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	17889902
MGI:5795669	M	MP:0004510	myositis	Dmd<mdx>/Y,Utrn<tm1Jrs>/Utrn<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	N	17889902
MGI:5795871	M	MP:0011088	neonatal lethality, incomplete penetrance	Ubl4a<tm1.2Arte>/Y	involves: C57BL/6	N	26195787
MGI:5795871	M	MP:0001262	decreased body weight	Ubl4a<tm1.2Arte>/Y	involves: C57BL/6	N	26195787
MGI:5795871	M	MP:0005438	abnormal glycogen homeostasis	Ubl4a<tm1.2Arte>/Y	involves: C57BL/6	N	26195787
MGI:5795871	M	MP:0001575	cyanosis	Ubl4a<tm1.2Arte>/Y	involves: C57BL/6	N	26195787
MGI:5795872	F	MP:0001575	cyanosis	Ubl4a<tm1.2Arte>/Ubl4a<tm1.2Arte>	involves: C57BL/6	N	26195787
MGI:5795872	F	MP:0001262	decreased body weight	Ubl4a<tm1.2Arte>/Ubl4a<tm1.2Arte>	involves: C57BL/6	N	26195787
MGI:5795872	F	MP:0011088	neonatal lethality, incomplete penetrance	Ubl4a<tm1.2Arte>/Ubl4a<tm1.2Arte>	involves: C57BL/6	N	26195787
MGI:5795872	F	MP:0005438	abnormal glycogen homeostasis	Ubl4a<tm1.2Arte>/Ubl4a<tm1.2Arte>	involves: C57BL/6	N	26195787
MGI:5795985	M	MP:0008261	arrest of male meiosis	Ppp2ca<tm1.1Jmli>/Ppp2ca<tm1.2Jmli>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	25628439
MGI:5795985	M	MP:0002662	abnormal cauda epididymis morphology	Ppp2ca<tm1.1Jmli>/Ppp2ca<tm1.2Jmli>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	25628439
MGI:5795985	M	MP:0001156	abnormal spermatogenesis	Ppp2ca<tm1.1Jmli>/Ppp2ca<tm1.2Jmli>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	25628439
MGI:5795985	M	MP:0002216	abnormal seminiferous tubule morphology	Ppp2ca<tm1.1Jmli>/Ppp2ca<tm1.2Jmli>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	25628439
MGI:5795985	M	MP:0004852	decreased testis weight	Ppp2ca<tm1.1Jmli>/Ppp2ca<tm1.2Jmli>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	25628439
MGI:5795985	M	MP:0001147	small testis	Ppp2ca<tm1.1Jmli>/Ppp2ca<tm1.2Jmli>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	25628439
MGI:5795985	M	MP:0001154	seminiferous tubule degeneration	Ppp2ca<tm1.1Jmli>/Ppp2ca<tm1.2Jmli>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	25628439
MGI:5795985	M	MP:0001925	male infertility	Ppp2ca<tm1.1Jmli>/Ppp2ca<tm1.2Jmli>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	25628439
MGI:5796139	M	MP:0000788	abnormal cerebral cortex morphology	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0005562	decreased mean corpuscular hemoglobin	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0000877	abnormal Purkinje cell morphology	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0008935	decreased mean platelet volume	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0005386	behavior/neurological phenotype	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	Y	24896637
MGI:5796139	M	MP:0011890	increased circulating ferritin level	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0005404	abnormal axon morphology	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0001405	impaired coordination	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0000780	abnormal corpus callosum morphology	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0020369	increased intestinal iron level	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0000953	abnormal oligodendrocyte morphology	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0010067	increased red blood cell distribution width	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0020368	decreased heart iron level	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0002757	decreased vertical activity	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0003631	nervous system phenotype	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	Y	24896637
MGI:5796139	M	MP:0020366	decreased brain iron level	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0002874	decreased hemoglobin content	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0020365	increased brain iron level	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0000832	abnormal thalamus morphology	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0002591	decreased mean corpuscular volume	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0001973	increased thermal nociceptive threshold	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0010375	increased kidney iron level	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0002810	microcytic anemia	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0005390	skeleton phenotype	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	Y	24896637
MGI:5796139	M	MP:0001770	abnormal iron level	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0004102	abnormal dorsal striatum morphology	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0000904	abnormal superior colliculus morphology	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0000208	decreased hematocrit	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0008807	increased liver iron level	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0005654	porphyria	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0003179	thrombocytopenia	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0001402	decreased locomotor activity	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0009940	abnormal hippocampus pyramidal cell morphology	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0009978	abnormal cerebellum white matter morphology	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796139	M	MP:0005637	abnormal iron homeostasis	Ireb2<tm1.1Eal>/Ireb2<tm1.1Eal>	B6J.129-Ireb2<tm1.1Eal>	N	24896637
MGI:5796280	M	MP:0004486	decreased response of heart to induced stress	Acp1<Gt(RRK222)Byg>/Acp1<Gt(RRK222)Byg>	C.129P2(B6)-Acp1<Gt(RRK222)Byg>	N	26213100
MGI:5796280	M	MP:0003223	decreased cardiomyocyte apoptosis	Acp1<Gt(RRK222)Byg>/Acp1<Gt(RRK222)Byg>	C.129P2(B6)-Acp1<Gt(RRK222)Byg>	N	26213100
MGI:5796280	M	MP:0001262	decreased body weight	Acp1<Gt(RRK222)Byg>/Acp1<Gt(RRK222)Byg>	C.129P2(B6)-Acp1<Gt(RRK222)Byg>	N	26213100
MGI:5796282	F	MP:0006271	abnormal involution of the mammary gland	Jak1<tm1Kuw>/Jak1<tm1Kuw>,Tg(MMTV-cre)1Mam/0	involves: 129X1/SvJ * FVB	N	27044867
MGI:5796283	F	MP:0006271	abnormal involution of the mammary gland	Jak1<tm1Kuw>/Jak1<tm1Kuw>,Tg(Wap-cre)11738Mam/0	involves: 129X1/SvJ * C57BL/6 * SJL	N	27044867
MGI:5796284	F	MP:0006271	abnormal involution of the mammary gland	Bmf<tm1.1Ast>/Bmf<tm1.1Ast>	involves: C57BL/6	N	27044867
MGI:5796293	M	MP:0001262	decreased body weight	Lmod2<Tn(pb-Act-RFP)1.1Zhu>/Lmod2<Tn(pb-Act-RFP)1.1Zhu>	involves: FVB/N	N	27274810
MGI:5796298	M	MP:0000693	spleen hyperplasia	Foxp3<tm2.1(EGFP/cre)Shori>/Y,Pdcd1<tm1Hon>/Pdcd1<tm1Hon>	involves: 129 * 129S2/SvPas * C57BL/6	N	27410049
MGI:5796298	M	MP:0013772	increased effector memory T-helper cell number	Foxp3<tm2.1(EGFP/cre)Shori>/Y,Pdcd1<tm1Hon>/Pdcd1<tm1Hon>	involves: 129 * 129S2/SvPas * C57BL/6	N	27410049
MGI:5796298	M	MP:0008102	lymph node hyperplasia	Foxp3<tm2.1(EGFP/cre)Shori>/Y,Pdcd1<tm1Hon>/Pdcd1<tm1Hon>	involves: 129 * 129S2/SvPas * C57BL/6	N	27410049
MGI:5796298	M	MP:0013295	pancreas atrophy	Foxp3<tm2.1(EGFP/cre)Shori>/Y,Pdcd1<tm1Hon>/Pdcd1<tm1Hon>	involves: 129 * 129S2/SvPas * C57BL/6	N	27410049
MGI:5796298	M	MP:0005350	increased susceptibility to autoimmune disorder	Foxp3<tm2.1(EGFP/cre)Shori>/Y,Pdcd1<tm1Hon>/Pdcd1<tm1Hon>	involves: 129 * 129S2/SvPas * C57BL/6	N	27410049
MGI:5796298	M	MP:0000702	enlarged lymph nodes	Foxp3<tm2.1(EGFP/cre)Shori>/Y,Pdcd1<tm1Hon>/Pdcd1<tm1Hon>	involves: 129 * 129S2/SvPas * C57BL/6	N	27410049
MGI:5796298	M	MP:0011887	decreased circulating lipase level	Foxp3<tm2.1(EGFP/cre)Shori>/Y,Pdcd1<tm1Hon>/Pdcd1<tm1Hon>	involves: 129 * 129S2/SvPas * C57BL/6	N	27410049
MGI:5796298	M	MP:0002083	premature death	Foxp3<tm2.1(EGFP/cre)Shori>/Y,Pdcd1<tm1Hon>/Pdcd1<tm1Hon>	involves: 129 * 129S2/SvPas * C57BL/6	N	27410049
MGI:5796298	M	MP:0000691	enlarged spleen	Foxp3<tm2.1(EGFP/cre)Shori>/Y,Pdcd1<tm1Hon>/Pdcd1<tm1Hon>	involves: 129 * 129S2/SvPas * C57BL/6	N	27410049
MGI:5796298	M	MP:0001869	pancreas inflammation	Foxp3<tm2.1(EGFP/cre)Shori>/Y,Pdcd1<tm1Hon>/Pdcd1<tm1Hon>	involves: 129 * 129S2/SvPas * C57BL/6	N	27410049
MGI:5796345	M	MP:0004974	decreased regulatory T cell number	Foxp3<tm2.1(EGFP/cre)Shori>/Y	involves: 129 * C57BL/6	N	27410049
MGI:5796346	F	MP:0002083	premature death	Foxp3<tm2.1(EGFP/cre)Shori>/Foxp3<tm2.1(EGFP/cre)Shori>,Pdcd1<tm1Hon>/Pdcd1<tm1Hon>	involves: 129 * 129S2/SvPas * C57BL/6	N	27410049
MGI:5796396	M	MP:0009238	coiled sperm flagellum	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6N	N	26621829
MGI:5796396	M	MP:0005389	reproductive system phenotype	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6N	Y	26621829
MGI:5796396	M	MP:0009230	abnormal sperm head morphology	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6N	N	26621829
MGI:5796396	M	MP:0001932	abnormal spermiogenesis	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6N	N	26621829
MGI:5796396	M	MP:0009376	abnormal manchette morphology	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6N	N	26621829
MGI:5796396	M	MP:0009232	abnormal sperm nucleus morphology	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6N	N	26621829
MGI:5796396	M	MP:0031374	abnormal manchette assembly	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6N	N	26621829
MGI:5796396	M	MP:0002631	abnormal epididymis morphology	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6N	N	26621829
MGI:5796396	M	MP:0001925	male infertility	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6N	N	26621829
MGI:5796396	M	MP:0002686	globozoospermia	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6N	N	26621829
MGI:5796396	M	MP:0031388	absent manchette	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6N	N	26621829
MGI:5796396	M	MP:0006380	abnormal spermatid morphology	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6N	N	26621829
MGI:5796396	M	MP:0009231	detached acrosome	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6N	N	26621829
MGI:5796492	M	MP:0009289	decreased epididymal fat pad weight	Tg(Pten)1Srn/0	involves: C57BL/6 * CBA	N	22405073
MGI:5796492	M	MP:0009133	decreased white fat cell size	Tg(Pten)1Srn/0	involves: C57BL/6 * CBA	N	22405073
MGI:5796560	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(MMTV-Erbb2)1Pv/0	involves: BALB/c * C57BL/6 * CD-1 * DBA	N	26941084
MGI:5796795	M	MP:0006380	abnormal spermatid morphology	Parp11<tm1(KOMP)Vlcg>/Parp11<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25673562
MGI:5796795	M	MP:0001925	male infertility	Parp11<tm1(KOMP)Vlcg>/Parp11<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25673562
MGI:5796795	M	MP:0001922	reduced male fertility	Parp11<tm1(KOMP)Vlcg>/Parp11<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25673562
MGI:5796795	M	MP:0005389	reproductive system phenotype	Parp11<tm1(KOMP)Vlcg>/Parp11<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	Y	25673562
MGI:5796795	M	MP:0009647	decreased fertilization frequency	Parp11<tm1(KOMP)Vlcg>/Parp11<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25673562
MGI:5796795	M	MP:0009232	abnormal sperm nucleus morphology	Parp11<tm1(KOMP)Vlcg>/Parp11<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25673562
MGI:5796795	M	MP:0001932	abnormal spermiogenesis	Parp11<tm1(KOMP)Vlcg>/Parp11<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25673562
MGI:5796795	M	MP:0009230	abnormal sperm head morphology	Parp11<tm1(KOMP)Vlcg>/Parp11<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25673562
MGI:5796795	M	MP:0005578	teratozoospermia	Parp11<tm1(KOMP)Vlcg>/Parp11<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25673562
MGI:5796832	M	MP:0005159	azoospermia	Top6bl<em1Arte>/Top6bl<em2Arte>	involves: C57BL/6NTac	N	26917764
MGI:5796832	F	MP:0011121	decreased primordial ovarian follicle number	Top6bl<em1Arte>/Top6bl<em2Arte>	involves: C57BL/6NTac	N	26917764
MGI:5796832	M	MP:0008261	arrest of male meiosis	Top6bl<em1Arte>/Top6bl<em2Arte>	involves: C57BL/6NTac	N	26917764
MGI:5796832	F	MP:0011125	decreased primary ovarian follicle number	Top6bl<em1Arte>/Top6bl<em2Arte>	involves: C57BL/6NTac	N	26917764
MGI:5796832	M	MP:0001147	small testis	Top6bl<em1Arte>/Top6bl<em2Arte>	involves: C57BL/6NTac	N	26917764
MGI:5796833	M	MP:0005159	azoospermia	Top6bl<em2Arte>/Top6bl<em2Arte>	involves: C57BL/6NTac	N	26917764
MGI:5796833	F	MP:0011121	decreased primordial ovarian follicle number	Top6bl<em2Arte>/Top6bl<em2Arte>	involves: C57BL/6NTac	N	26917764
MGI:5796833	F	MP:0011125	decreased primary ovarian follicle number	Top6bl<em2Arte>/Top6bl<em2Arte>	involves: C57BL/6NTac	N	26917764
MGI:5796833	M	MP:0008261	arrest of male meiosis	Top6bl<em2Arte>/Top6bl<em2Arte>	involves: C57BL/6NTac	N	26917764
MGI:5796833	M	MP:0001147	small testis	Top6bl<em2Arte>/Top6bl<em2Arte>	involves: C57BL/6NTac	N	26917764
MGI:5797312	M	MP:0002073	abnormal hair growth	1700008O03Rik<tm1a(KOMP)Wtsi>/1700008O03Rik<tm1a(KOMP)Wtsi>	C57BL/6N-1700008O03Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797312	M	MP:0002608	increased hematocrit	1700008O03Rik<tm1a(KOMP)Wtsi>/1700008O03Rik<tm1a(KOMP)Wtsi>	C57BL/6N-1700008O03Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797313	M	MP:0000063	decreased bone mineral density	Liat1<tm1.1(KOMP)Vlcg>/Liat1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Liat1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797313	M	MP:0002941	increased circulating alanine transaminase level	Liat1<tm1.1(KOMP)Vlcg>/Liat1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Liat1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797314	M	MP:0001925	male infertility	H2bl1<tm1b(EUCOMM)Wtsi>/H2bl1<tm1b(EUCOMM)Wtsi>	C57BL/6N-H2bl1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797315	F	MP:0005554	decreased circulating creatinine level	2610318N02Rik<tm1b(EUCOMM)Wtsi>/2610318N02Rik<tm1b(EUCOMM)Wtsi>	C57BL/6N-2610318N02Rik<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797316	M	MP:0000745	tremors	Rtraf<tm1b(EUCOMM)Hmgu>/Rtraf<+>	C57BL/6N-Rtraf<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797316	M	MP:0001417	decreased exploration in new environment	Rtraf<tm1b(EUCOMM)Hmgu>/Rtraf<+>	C57BL/6N-Rtraf<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797317	F	MP:0002968	increased circulating alkaline phosphatase level	2700097O09Rik<tm1.1(KOMP)Vlcg>/2700097O09Rik<tm1.1(KOMP)Vlcg>	C57BL/6N-2700097O09Rik<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5797317	M	MP:0002631	abnormal epididymis morphology	2700097O09Rik<tm1.1(KOMP)Vlcg>/2700097O09Rik<tm1.1(KOMP)Vlcg>	C57BL/6N-2700097O09Rik<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5797317	F	MP:0000598	abnormal liver morphology	2700097O09Rik<tm1.1(KOMP)Vlcg>/2700097O09Rik<tm1.1(KOMP)Vlcg>	C57BL/6N-2700097O09Rik<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5797317	M	MP:0001513	limb grasping	2700097O09Rik<tm1.1(KOMP)Vlcg>/2700097O09Rik<tm1.1(KOMP)Vlcg>	C57BL/6N-2700097O09Rik<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5797317	M	MP:0004931	enlarged epididymis	2700097O09Rik<tm1.1(KOMP)Vlcg>/2700097O09Rik<tm1.1(KOMP)Vlcg>	C57BL/6N-2700097O09Rik<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5797318	M	MP:0001146	abnormal testis morphology	Cyren<tm1.1(KOMP)Vlcg>/Cyren<tm1.1(KOMP)Vlcg>	C57BL/6N-Cyren<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797318	M	MP:0000274	enlarged heart	Cyren<tm1.1(KOMP)Vlcg>/Cyren<tm1.1(KOMP)Vlcg>	C57BL/6N-Cyren<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797318	M	MP:0001147	small testis	Cyren<tm1.1(KOMP)Vlcg>/Cyren<tm1.1(KOMP)Vlcg>	C57BL/6N-Cyren<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797318	M	MP:0000266	abnormal heart morphology	Cyren<tm1.1(KOMP)Vlcg>/Cyren<tm1.1(KOMP)Vlcg>	C57BL/6N-Cyren<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797319	M	MP:0010025	decreased total body fat amount	4921536K21Rik<tm1a(KOMP)Wtsi>/4921536K21Rik<tm1a(KOMP)Wtsi>	C57BL/6N-4921536K21Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797320	M	MP:0000219	increased neutrophil cell number	Dnaaf9<tm1b(EUCOMM)Hmgu>/Dnaaf9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dnaaf9<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5797320	F	MP:0009142	decreased prepulse inhibition	Dnaaf9<tm1b(EUCOMM)Hmgu>/Dnaaf9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dnaaf9<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5797321	M	MP:0005419	decreased circulating serum albumin level	4930404H24Rik<tm1a(KOMP)Wtsi>/4930404H24Rik<tm1a(KOMP)Wtsi>	C57BL/6N-4930404H24Rik<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797322	F	MP:0001304	cataract	Bltp1<tm1b(EUCOMM)Hmgu>/Bltp1<+>	C57BL/6N-Bltp1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797322	M	MP:0005293	impaired glucose tolerance	Bltp1<tm1b(EUCOMM)Hmgu>/Bltp1<+>	C57BL/6N-Bltp1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797322	F	MP:0001289	persistence of hyaloid vascular system	Bltp1<tm1b(EUCOMM)Hmgu>/Bltp1<+>	C57BL/6N-Bltp1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797322	F	MP:0001325	abnormal retina morphology	Bltp1<tm1b(EUCOMM)Hmgu>/Bltp1<+>	C57BL/6N-Bltp1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797323	M	MP:0001402	decreased locomotor activity	Bltp1<tm1b(EUCOMM)Hmgu>/Bltp1<+>	B6N(Cg)-Bltp1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797323	M	MP:0002797	increased thigmotaxis	Bltp1<tm1b(EUCOMM)Hmgu>/Bltp1<+>	B6N(Cg)-Bltp1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797323	M	MP:0004924	abnormal behavior	Bltp1<tm1b(EUCOMM)Hmgu>/Bltp1<+>	B6N(Cg)-Bltp1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797323	F	MP:0002833	increased heart weight	Bltp1<tm1b(EUCOMM)Hmgu>/Bltp1<+>	B6N(Cg)-Bltp1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797324	F	MP:0010123	increased bone mineral content	4933428G20Rik<tm1.1(KOMP)Vlcg>/4933428G20Rik<tm1.1(KOMP)Vlcg>	C57BL/6N-4933428G20Rik<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5797324	F	MP:0005343	increased circulating aspartate transaminase level	4933428G20Rik<tm1.1(KOMP)Vlcg>/4933428G20Rik<tm1.1(KOMP)Vlcg>	C57BL/6N-4933428G20Rik<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5797325	M	MP:0002941	increased circulating alanine transaminase level	4933434E20Rik<tm1a(EUCOMM)Wtsi>/4933434E20Rik<+>	C57BL/6N-4933434E20Rik<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797325	M	MP:0000186	decreased circulating HDL cholesterol level	4933434E20Rik<tm1a(EUCOMM)Wtsi>/4933434E20Rik<+>	C57BL/6N-4933434E20Rik<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797325	M	MP:0010088	decreased circulating fructosamine level	4933434E20Rik<tm1a(EUCOMM)Wtsi>/4933434E20Rik<+>	C57BL/6N-4933434E20Rik<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797325	M	MP:0005419	decreased circulating serum albumin level	4933434E20Rik<tm1a(EUCOMM)Wtsi>/4933434E20Rik<+>	C57BL/6N-4933434E20Rik<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797325	M	MP:0005179	decreased circulating cholesterol level	4933434E20Rik<tm1a(EUCOMM)Wtsi>/4933434E20Rik<+>	C57BL/6N-4933434E20Rik<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797327	M	MP:0005293	impaired glucose tolerance	Aak1<tm1b(EUCOMM)Hmgu>/Aak1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aak1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:5797327	F	MP:0002941	increased circulating alanine transaminase level	Aak1<tm1b(EUCOMM)Hmgu>/Aak1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aak1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:5797327	M	MP:0009141	increased prepulse inhibition	Aak1<tm1b(EUCOMM)Hmgu>/Aak1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aak1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:5797327	M	MP:0001489	decreased startle reflex	Aak1<tm1b(EUCOMM)Hmgu>/Aak1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aak1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:5797327	F	MP:0003795	abnormal bone structure	Aak1<tm1b(EUCOMM)Hmgu>/Aak1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aak1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:5797327	F	MP:0005343	increased circulating aspartate transaminase level	Aak1<tm1b(EUCOMM)Hmgu>/Aak1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aak1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:5797327	M	MP:0005419	decreased circulating serum albumin level	Aak1<tm1b(EUCOMM)Hmgu>/Aak1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aak1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:5797328	M	MP:0004931	enlarged epididymis	AB124611<tm1.1(KOMP)Vlcg>/AB124611<tm1.1(KOMP)Vlcg>	C57BL/6N-AB124611<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797328	M	MP:0002631	abnormal epididymis morphology	AB124611<tm1.1(KOMP)Vlcg>/AB124611<tm1.1(KOMP)Vlcg>	C57BL/6N-AB124611<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797328	F	MP:0010393	shortened QRS complex duration	AB124611<tm1.1(KOMP)Vlcg>/AB124611<tm1.1(KOMP)Vlcg>	C57BL/6N-AB124611<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797328	M	MP:0000266	abnormal heart morphology	AB124611<tm1.1(KOMP)Vlcg>/AB124611<tm1.1(KOMP)Vlcg>	C57BL/6N-AB124611<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797328	M	MP:0002135	abnormal kidney morphology	AB124611<tm1.1(KOMP)Vlcg>/AB124611<tm1.1(KOMP)Vlcg>	C57BL/6N-AB124611<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797328	M	MP:0000274	enlarged heart	AB124611<tm1.1(KOMP)Vlcg>/AB124611<tm1.1(KOMP)Vlcg>	C57BL/6N-AB124611<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797329	M	MP:0009142	decreased prepulse inhibition	Abca13<tm1b(EUCOMM)Wtsi>/Abca13<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abca13<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5797329	F	MP:0002966	decreased circulating alkaline phosphatase level	Abca13<tm1b(EUCOMM)Wtsi>/Abca13<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abca13<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5797332	F	MP:0013630	increased bone trabecular spacing	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	F	MP:0002968	increased circulating alkaline phosphatase level	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	M	MP:0005292	improved glucose tolerance	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	M	MP:0000195	decreased circulating calcium level	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	M	MP:0010123	increased bone mineral content	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	M	MP:0005567	decreased circulating total protein level	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	F	MP:0010869	decreased bone trabecula number	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	F	MP:0005565	increased blood urea nitrogen level	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	M	MP:0001513	limb grasping	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	M	MP:0003960	increased lean body mass	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	M	MP:0005419	decreased circulating serum albumin level	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	M	MP:0003179	thrombocytopenia	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	F	MP:0005553	increased circulating creatinine level	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	M	MP:0010025	decreased total body fat amount	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	M	MP:0001257	increased body length	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	M	MP:0001406	abnormal gait	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	M	MP:0000062	increased bone mineral density	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797332	M	MP:0002644	decreased circulating triglyceride level	Acbd5<tm1b(EUCOMM)Wtsi>/Acbd5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acbd5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797333	F	MP:0002135	abnormal kidney morphology	Acot4<tm1b(KOMP)Wtsi>/Acot4<tm1b(KOMP)Wtsi>	C57BL/6N-Acot4<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797334	M	MP:0010088	decreased circulating fructosamine level	Actl10<tm1a(EUCOMM)Wtsi>/Actl10<tm1a(EUCOMM)Wtsi>	C57BL/6N-Actl10<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797335	M	MP:0001392	abnormal locomotor behavior	Adam11<tm1b(KOMP)Mbp>/Adam11<tm1b(KOMP)Mbp>	C57BL/6N-Adam11<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:5797339	M	MP:0010052	increased grip strength	Adamtsl5<tm1b(EUCOMM)Hmgu>/Adamtsl5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adamtsl5<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797340	M	MP:0005565	increased blood urea nitrogen level	Adcy6<tm1.1(KOMP)Vlcg>/Adcy6<tm1.1(KOMP)Vlcg>	C57BL/6N-Adcy6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797341	M	MP:0002079	increased circulating insulin level	Adcy9<tm1b(EUCOMM)Wtsi>/Adcy9<+>	C57BL/6N-Adcy9<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797343	F	MP:0002060	abnormal skin morphology	Adgrl3<tm1.1(KOMP)Vlcg>/Adgrl3<tm1.1(KOMP)Vlcg>	C57BL/6N-Adgrl3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797344	M	MP:0002874	decreased hemoglobin content	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	C57BL/6N-Adig<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797346	M	MP:0001513	limb grasping	Adipor2<tm1b(EUCOMM)Hmgu>/Adipor2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797346	M	MP:0010053	decreased grip strength	Adipor2<tm1b(EUCOMM)Hmgu>/Adipor2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797346	M	MP:0001147	small testis	Adipor2<tm1b(EUCOMM)Hmgu>/Adipor2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797346	M	MP:0001925	male infertility	Adipor2<tm1b(EUCOMM)Hmgu>/Adipor2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797346	M	MP:0005016	decreased lymphocyte cell number	Adipor2<tm1b(EUCOMM)Hmgu>/Adipor2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797346	M	MP:0000219	increased neutrophil cell number	Adipor2<tm1b(EUCOMM)Hmgu>/Adipor2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797347	F	MP:0001312	abnormal cornea morphology	Ahsa2<tm1b(EUCOMM)Wtsi>/Ahsa2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ahsa2<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797347	F	MP:0011965	decreased total retina thickness	Ahsa2<tm1b(EUCOMM)Wtsi>/Ahsa2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ahsa2<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797349	M	MP:0008259	abnormal optic disk morphology	Aif1<tm1.1(KOMP)Wtsi>/Aif1<tm1.1(KOMP)Wtsi>	C57BL/6N-Aif1<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5797349	F	MP:0001325	abnormal retina morphology	Aif1<tm1.1(KOMP)Wtsi>/Aif1<tm1.1(KOMP)Wtsi>	C57BL/6N-Aif1<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5797349	F	MP:0005566	decreased blood urea nitrogen level	Aif1<tm1.1(KOMP)Wtsi>/Aif1<tm1.1(KOMP)Wtsi>	C57BL/6N-Aif1<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5797349	F	MP:0003961	decreased lean body mass	Aif1<tm1.1(KOMP)Wtsi>/Aif1<tm1.1(KOMP)Wtsi>	C57BL/6N-Aif1<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5797350	M	MP:0009142	decreased prepulse inhibition	Aire<tm1.1(NCOM)Mfgc>/Aire<tm1.1(NCOM)Mfgc>	C57BL/6N-Aire<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797350	F	MP:0000220	increased monocyte cell number	Aire<tm1.1(NCOM)Mfgc>/Aire<tm1.1(NCOM)Mfgc>	C57BL/6N-Aire<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797351	M	MP:0000221	decreased leukocyte cell number	Akap11<tm1b(EUCOMM)Hmgu>/Akap11<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Akap11<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797352	M	MP:0010052	increased grip strength	Akr1d1<tm1.1(KOMP)Vlcg>/Akr1d1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Akr1d1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797352	M	MP:0001289	persistence of hyaloid vascular system	Akr1d1<tm1.1(KOMP)Vlcg>/Akr1d1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Akr1d1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797352	F	MP:0001399	hyperactivity	Akr1d1<tm1.1(KOMP)Vlcg>/Akr1d1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Akr1d1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797353	F	MP:0002135	abnormal kidney morphology	Aldoc<tm1.1(KOMP)Vlcg>/Aldoc<tm1.1(KOMP)Vlcg>	C57BL/6N-Aldoc<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797355	F	MP:0005278	abnormal cholesterol homeostasis	Alg1<tm1b(KOMP)Wtsi>/Alg1<+>	C57BL/6N-Alg1<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797355	F	MP:0000218	increased leukocyte cell number	Alg1<tm1b(KOMP)Wtsi>/Alg1<+>	C57BL/6N-Alg1<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797355	F	MP:0005011	increased eosinophil cell number	Alg1<tm1b(KOMP)Wtsi>/Alg1<+>	C57BL/6N-Alg1<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797355	M	MP:0002075	abnormal coat/hair pigmentation	Alg1<tm1b(KOMP)Wtsi>/Alg1<+>	C57BL/6N-Alg1<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797355	F	MP:0002606	increased basophil cell number	Alg1<tm1b(KOMP)Wtsi>/Alg1<+>	C57BL/6N-Alg1<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797355	F	MP:0005013	increased lymphocyte cell number	Alg1<tm1b(KOMP)Wtsi>/Alg1<+>	C57BL/6N-Alg1<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797356	F	MP:0005140	decreased cardiac muscle contractility	Alpk3<tm1b(EUCOMM)Hmgu>/Alpk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Alpk3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797356	F	MP:0002753	dilated heart left ventricle	Alpk3<tm1b(EUCOMM)Hmgu>/Alpk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Alpk3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797356	F	MP:0010579	increased heart left ventricle size	Alpk3<tm1b(EUCOMM)Hmgu>/Alpk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Alpk3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797356	F	MP:0002953	thick ventricular wall	Alpk3<tm1b(EUCOMM)Hmgu>/Alpk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Alpk3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797356	F	MP:0002833	increased heart weight	Alpk3<tm1b(EUCOMM)Hmgu>/Alpk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Alpk3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797357	M	MP:0000274	enlarged heart	Amigo3<tm1.1(KOMP)Vlcg>/Amigo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Amigo3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797358	M	MP:0002590	increased mean corpuscular volume	Anapc13<tm2b(EUCOMM)Wtsi>/Anapc13<+>	C57BL/6N-Anapc13<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5797358	M	MP:0001510	abnormal coat appearance	Anapc13<tm2b(EUCOMM)Wtsi>/Anapc13<+>	C57BL/6N-Anapc13<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5797359	M	MP:0010378	increased respiratory quotient	Ang6<tm1.1(KOMP)Vlcg>/Ang6<tm1.1(KOMP)Vlcg>	C57BL/6N-Ang6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797360	M	MP:0013279	increased fasting circulating glucose level	Ankib1<tm1b(EUCOMM)Hmgu>/Ankib1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ankib1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797360	M	MP:0001513	limb grasping	Ankib1<tm1b(EUCOMM)Hmgu>/Ankib1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ankib1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797360	F	MP:0002764	short tibia	Ankib1<tm1b(EUCOMM)Hmgu>/Ankib1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ankib1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797360	F	MP:0002968	increased circulating alkaline phosphatase level	Ankib1<tm1b(EUCOMM)Hmgu>/Ankib1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ankib1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797361	M	MP:0001258	decreased body length	Ankrd1<tm1.1(KOMP)Vlcg>/Ankrd1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ankrd1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797362	F	MP:0002941	increased circulating alanine transaminase level	Apbb2<tm1.1(KOMP)Vlcg>/Apbb2<+>	C57BL/6N-Apbb2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797362	M	MP:0002092	abnormal eye morphology	Apbb2<tm1.1(KOMP)Vlcg>/Apbb2<+>	C57BL/6N-Apbb2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797362	M	MP:0002060	abnormal skin morphology	Apbb2<tm1.1(KOMP)Vlcg>/Apbb2<+>	C57BL/6N-Apbb2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797362	F	MP:0005343	increased circulating aspartate transaminase level	Apbb2<tm1.1(KOMP)Vlcg>/Apbb2<+>	C57BL/6N-Apbb2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797362	M	MP:0005630	increased lung weight	Apbb2<tm1.1(KOMP)Vlcg>/Apbb2<+>	C57BL/6N-Apbb2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797364	F	MP:0001120	abnormal uterus morphology	Apom<tm1.1(KOMP)Vlcg>/Apom<tm1.1(KOMP)Vlcg>	C57BL/6N-Apom<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797364	F	MP:0002941	increased circulating alanine transaminase level	Apom<tm1.1(KOMP)Vlcg>/Apom<tm1.1(KOMP)Vlcg>	C57BL/6N-Apom<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797364	M	MP:0004931	enlarged epididymis	Apom<tm1.1(KOMP)Vlcg>/Apom<tm1.1(KOMP)Vlcg>	C57BL/6N-Apom<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797364	F	MP:0009709	hydrometra	Apom<tm1.1(KOMP)Vlcg>/Apom<tm1.1(KOMP)Vlcg>	C57BL/6N-Apom<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797367	M	MP:0002546	mydriasis	Aqp11<tm1.1(KOMP)Vlcg>/Aqp11<+>	B6N(Cg)-Aqp11<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797367	F	MP:0000221	decreased leukocyte cell number	Aqp11<tm1.1(KOMP)Vlcg>/Aqp11<+>	B6N(Cg)-Aqp11<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797368	F	MP:0003020	decreased circulating chloride level	Aqp1<tm1b(EUCOMM)Wtsi>/Aqp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aqp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797368	M	MP:0000063	decreased bone mineral density	Aqp1<tm1b(EUCOMM)Wtsi>/Aqp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aqp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797368	F	MP:0005553	increased circulating creatinine level	Aqp1<tm1b(EUCOMM)Wtsi>/Aqp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aqp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797368	F	MP:0010053	decreased grip strength	Aqp1<tm1b(EUCOMM)Wtsi>/Aqp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aqp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797368	F	MP:0010025	decreased total body fat amount	Aqp1<tm1b(EUCOMM)Wtsi>/Aqp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aqp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797368	F	MP:0001556	increased circulating HDL cholesterol level	Aqp1<tm1b(EUCOMM)Wtsi>/Aqp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aqp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797368	F	MP:0010124	decreased bone mineral content	Aqp1<tm1b(EUCOMM)Wtsi>/Aqp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aqp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797368	F	MP:0005178	increased circulating cholesterol level	Aqp1<tm1b(EUCOMM)Wtsi>/Aqp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aqp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797368	F	MP:0005568	increased circulating total protein level	Aqp1<tm1b(EUCOMM)Wtsi>/Aqp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aqp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797368	M	MP:0008806	increased circulating amylase level	Aqp1<tm1b(EUCOMM)Wtsi>/Aqp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aqp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797368	M	MP:0005293	impaired glucose tolerance	Aqp1<tm1b(EUCOMM)Wtsi>/Aqp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aqp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797368	M	MP:0000219	increased neutrophil cell number	Aqp1<tm1b(EUCOMM)Wtsi>/Aqp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aqp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797370	M	MP:0002590	increased mean corpuscular volume	Areg<tm2b(EUCOMM)Hmgu>/Areg<tm2b(EUCOMM)Hmgu>	C57BL/6N-Areg<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797371	M	MP:0001325	abnormal retina morphology	Arf3<tm1b(EUCOMM)Hmgu>/Arf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Arf3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797371	F	MP:0002699	abnormal vitreous body morphology	Arf3<tm1b(EUCOMM)Hmgu>/Arf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Arf3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797371	M	MP:0001304	cataract	Arf3<tm1b(EUCOMM)Hmgu>/Arf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Arf3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797371	F	MP:0002792	abnormal retina vasculature morphology	Arf3<tm1b(EUCOMM)Hmgu>/Arf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Arf3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797372	M	MP:0005560	decreased circulating glucose level	Arhgap17<tm1b(EUCOMM)Wtsi>/Arhgap17<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arhgap17<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797372	M	MP:0005292	improved glucose tolerance	Arhgap17<tm1b(EUCOMM)Wtsi>/Arhgap17<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arhgap17<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797373	M	MP:0000702	enlarged lymph nodes	Arhgef6<tm2e.1(EUCOMM)Wtsi>/Y	C57BL/6N-Arhgef6<tm2e.1(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797374	F	MP:0005016	decreased lymphocyte cell number	Arhgef6<tm2e.1(EUCOMM)Wtsi>/Arhgef6<tm2e.1(EUCOMM)Wtsi>	C57BL/6N-Arhgef6<tm2e.1(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797374	F	MP:0005343	increased circulating aspartate transaminase level	Arhgef6<tm2e.1(EUCOMM)Wtsi>/Arhgef6<tm2e.1(EUCOMM)Wtsi>	C57BL/6N-Arhgef6<tm2e.1(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797374	F	MP:0005627	increased circulating potassium level	Arhgef6<tm2e.1(EUCOMM)Wtsi>/Arhgef6<tm2e.1(EUCOMM)Wtsi>	C57BL/6N-Arhgef6<tm2e.1(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797377	M	MP:0009142	decreased prepulse inhibition	Arl8b<tm1.1(NCOM)Mfgc>/Arl8b<+>	C57BL/6N-Arl8b<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797377	F	MP:0005565	increased blood urea nitrogen level	Arl8b<tm1.1(NCOM)Mfgc>/Arl8b<+>	C57BL/6N-Arl8b<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797378	M	MP:0004509	abnormal pelvic girdle bone morphology	Arl8b<tm1.1(NCOM)Mfgc>/Arl8b<tm1.1(NCOM)Mfgc>	C57BL/6N-Arl8b<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797379	M	MP:0000274	enlarged heart	Arl9<tm1.1(KOMP)Vlcg>/Arl9<tm1.1(KOMP)Vlcg>	C57BL/6N-Arl9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797379	M	MP:0000266	abnormal heart morphology	Arl9<tm1.1(KOMP)Vlcg>/Arl9<tm1.1(KOMP)Vlcg>	C57BL/6N-Arl9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797381	F	MP:0001406	abnormal gait	Arvcf<tm1e(EUCOMM)Wtsi>/Arvcf<tm1e(EUCOMM)Wtsi>	C57BL/6N-Arvcf<tm1e(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5797381	M	MP:0001303	abnormal lens morphology	Arvcf<tm1e(EUCOMM)Wtsi>/Arvcf<tm1e(EUCOMM)Wtsi>	C57BL/6N-Arvcf<tm1e(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5797381	F	MP:0002968	increased circulating alkaline phosphatase level	Arvcf<tm1e(EUCOMM)Wtsi>/Arvcf<tm1e(EUCOMM)Wtsi>	C57BL/6N-Arvcf<tm1e(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5797381	M	MP:0001304	cataract	Arvcf<tm1e(EUCOMM)Wtsi>/Arvcf<tm1e(EUCOMM)Wtsi>	C57BL/6N-Arvcf<tm1e(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5797382	F	MP:0006243	impaired pupillary reflex	Ash1l<tm2b(EUCOMM)Hmgu>/Ash1l<+>	C57BL/6N-Ash1l<tm2b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5797382	M	MP:0001510	abnormal coat appearance	Ash1l<tm2b(EUCOMM)Hmgu>/Ash1l<+>	C57BL/6N-Ash1l<tm2b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5797382	M	MP:0002833	increased heart weight	Ash1l<tm2b(EUCOMM)Hmgu>/Ash1l<+>	C57BL/6N-Ash1l<tm2b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5797384	M	MP:0001489	decreased startle reflex	Aspa<tm1b(EUCOMM)Wtsi>/Aspa<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aspa<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5797384	F	MP:0001417	decreased exploration in new environment	Aspa<tm1b(EUCOMM)Wtsi>/Aspa<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aspa<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5797384	M	MP:0001513	limb grasping	Aspa<tm1b(EUCOMM)Wtsi>/Aspa<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aspa<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5797384	M	MP:0002590	increased mean corpuscular volume	Aspa<tm1b(EUCOMM)Wtsi>/Aspa<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aspa<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5797384	F	MP:0002968	increased circulating alkaline phosphatase level	Aspa<tm1b(EUCOMM)Wtsi>/Aspa<tm1b(EUCOMM)Wtsi>	C57BL/6N-Aspa<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5797385	M	MP:0005564	increased hemoglobin content	Atl2<tm2b(EUCOMM)Hmgu>/Atl2<+>	C57BL/6N-Atl2<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797385	M	MP:0003961	decreased lean body mass	Atl2<tm2b(EUCOMM)Hmgu>/Atl2<+>	C57BL/6N-Atl2<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797385	M	MP:0010068	decreased red blood cell distribution width	Atl2<tm2b(EUCOMM)Hmgu>/Atl2<+>	C57BL/6N-Atl2<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797385	M	MP:0005013	increased lymphocyte cell number	Atl2<tm2b(EUCOMM)Hmgu>/Atl2<+>	C57BL/6N-Atl2<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797385	M	MP:0002591	decreased mean corpuscular volume	Atl2<tm2b(EUCOMM)Hmgu>/Atl2<+>	C57BL/6N-Atl2<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797385	M	MP:0000222	decreased neutrophil cell number	Atl2<tm2b(EUCOMM)Hmgu>/Atl2<+>	C57BL/6N-Atl2<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797386	M	MP:0009142	decreased prepulse inhibition	Atp5f1b<tm1b(EUCOMM)Hmgu>/Atp5f1b<+>	C57BL/6N-Atp5f1b<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5797388	F	MP:0005287	narrow eye opening	Dmac2l<tm1b(EUCOMM)Hmgu>/Dmac2l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dmac2l<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797389	M	MP:0002590	increased mean corpuscular volume	Atp6v1c1<tm1b(NCOM)Mfgc>/Atp6v1c1<+>	C57BL/6N-Atp6v1c1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797389	M	MP:0000218	increased leukocyte cell number	Atp6v1c1<tm1b(NCOM)Mfgc>/Atp6v1c1<+>	C57BL/6N-Atp6v1c1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797391	F	MP:0012121	sclerocornea	Aurka<tm1b(EUCOMM)Hmgu>/Aurka<+>	B6N(Cg)-Aurka<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797391	F	MP:0003795	abnormal bone structure	Aurka<tm1b(EUCOMM)Hmgu>/Aurka<+>	B6N(Cg)-Aurka<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797392	M	MP:0003928	increased heart rate variability	Avpi1<tm1b(EUCOMM)Hmgu>/Avpi1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Avpi1<tm1b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5797394	M	MP:0000274	enlarged heart	B3gnt7<tm1e.1(KOMP)Wtsi>/B3gnt7<tm1e.1(KOMP)Wtsi>	C57BL/6N-B3gnt7<tm1e.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797394	M	MP:0002574	increased vertical activity	B3gnt7<tm1e.1(KOMP)Wtsi>/B3gnt7<tm1e.1(KOMP)Wtsi>	C57BL/6N-B3gnt7<tm1e.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797394	M	MP:0000691	enlarged spleen	B3gnt7<tm1e.1(KOMP)Wtsi>/B3gnt7<tm1e.1(KOMP)Wtsi>	C57BL/6N-B3gnt7<tm1e.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797395	F	MP:0001399	hyperactivity	B4gat1<tm1.1(KOMP)Vlcg>/B4gat1<+>	C57BL/6N-B4gat1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797396	M	MP:0011965	decreased total retina thickness	Bahd1<tm2b(KOMP)Wtsi>/Bahd1<+>	C57BL/6N-Bahd1<tm2b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797396	M	MP:0001488	increased startle reflex	Bahd1<tm2b(KOMP)Wtsi>/Bahd1<+>	C57BL/6N-Bahd1<tm2b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797396	M	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number	Bahd1<tm2b(KOMP)Wtsi>/Bahd1<+>	C57BL/6N-Bahd1<tm2b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797396	M	MP:0001402	decreased locomotor activity	Bahd1<tm2b(KOMP)Wtsi>/Bahd1<+>	C57BL/6N-Bahd1<tm2b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797396	M	MP:0000221	decreased leukocyte cell number	Bahd1<tm2b(KOMP)Wtsi>/Bahd1<+>	C57BL/6N-Bahd1<tm2b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797397	M	MP:0001147	small testis	Baiap2<tm1b(KOMP)Wtsi>/Baiap2<+>	C57BL/6N-Baiap2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797397	M	MP:0001146	abnormal testis morphology	Baiap2<tm1b(KOMP)Wtsi>/Baiap2<+>	C57BL/6N-Baiap2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797397	F	MP:0000195	decreased circulating calcium level	Baiap2<tm1b(KOMP)Wtsi>/Baiap2<+>	C57BL/6N-Baiap2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797397	M	MP:0003179	thrombocytopenia	Baiap2<tm1b(KOMP)Wtsi>/Baiap2<+>	C57BL/6N-Baiap2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797398	F	MP:0000274	enlarged heart	Bbox1<tm1b(KOMP)Wtsi>/Bbox1<tm1b(KOMP)Wtsi>	C57BL/6N-Bbox1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797400	M	MP:0002075	abnormal coat/hair pigmentation	Bend3<tm1b(KOMP)Mbp>/Bend3<+>	C57BL/6N-Bend3<tm1b(KOMP)Mbp>/Nju	N	MGI:5576271
MGI:5797401	M	MP:0001399	hyperactivity	Bex6<tm1.1(KOMP)Vlcg>/Bex6<tm1.1(KOMP)Vlcg>	B6N(Cg)-Bex6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797401	M	MP:0000218	increased leukocyte cell number	Bex6<tm1.1(KOMP)Vlcg>/Bex6<tm1.1(KOMP)Vlcg>	B6N(Cg)-Bex6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797402	M	MP:0002833	increased heart weight	Bhlhe40<tm1b(KOMP)Wtsi>/Bhlhe40<tm1b(KOMP)Wtsi>	B6N(Cg)-Bhlhe40<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797402	M	MP:0013278	decreased fasting circulating glucose level	Bhlhe40<tm1b(KOMP)Wtsi>/Bhlhe40<tm1b(KOMP)Wtsi>	B6N(Cg)-Bhlhe40<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797403	F	MP:0010053	decreased grip strength	Bicd1<tm1.1(KOMP)Wtsi>/Bicd1<tm1.1(KOMP)Wtsi>	C57BL/6N-Bicd1<tm1.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797403	M	MP:0001489	decreased startle reflex	Bicd1<tm1.1(KOMP)Wtsi>/Bicd1<tm1.1(KOMP)Wtsi>	C57BL/6N-Bicd1<tm1.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797403	F	MP:0009142	decreased prepulse inhibition	Bicd1<tm1.1(KOMP)Wtsi>/Bicd1<tm1.1(KOMP)Wtsi>	C57BL/6N-Bicd1<tm1.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797404	F	MP:0005292	improved glucose tolerance	Bmp10<tm3b(EUCOMM)Hmgu>/Bmp10<+>	C57BL/6N-Bmp10<tm3b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5797404	M	MP:0001417	decreased exploration in new environment	Bmp10<tm3b(EUCOMM)Hmgu>/Bmp10<+>	C57BL/6N-Bmp10<tm3b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5797405	F	MP:0002874	decreased hemoglobin content	Bola2<tm1(KOMP)Wtsi>/Bola2<tm1(KOMP)Wtsi>	C57BL/6N-Bola2<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797405	F	MP:0002591	decreased mean corpuscular volume	Bola2<tm1(KOMP)Wtsi>/Bola2<tm1(KOMP)Wtsi>	C57BL/6N-Bola2<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797405	F	MP:0005292	improved glucose tolerance	Bola2<tm1(KOMP)Wtsi>/Bola2<tm1(KOMP)Wtsi>	C57BL/6N-Bola2<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797406	F	MP:0009709	hydrometra	Bpifb1<tm1b(KOMP)Wtsi>/Bpifb1<tm1b(KOMP)Wtsi>	C57BL/6N-Bpifb1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797406	F	MP:0001120	abnormal uterus morphology	Bpifb1<tm1b(KOMP)Wtsi>/Bpifb1<tm1b(KOMP)Wtsi>	C57BL/6N-Bpifb1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797406	F	MP:0005343	increased circulating aspartate transaminase level	Bpifb1<tm1b(KOMP)Wtsi>/Bpifb1<tm1b(KOMP)Wtsi>	C57BL/6N-Bpifb1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797407	M	MP:0002282	abnormal trachea morphology	C1ra<tm1.1(KOMP)Vlcg>/C1ra<tm1.1(KOMP)Vlcg>	C57BL/6N-C1ra<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797408	M	MP:0000274	enlarged heart	Cabp4<tm1.1(KOMP)Vlcg>/Cabp4<tm1.1(KOMP)Vlcg>	C57BL/6N-Cabp4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797408	M	MP:0000266	abnormal heart morphology	Cabp4<tm1.1(KOMP)Vlcg>/Cabp4<tm1.1(KOMP)Vlcg>	C57BL/6N-Cabp4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797408	M	MP:0002152	abnormal brain morphology	Cabp4<tm1.1(KOMP)Vlcg>/Cabp4<tm1.1(KOMP)Vlcg>	C57BL/6N-Cabp4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797408	M	MP:0001891	hydrocephaly	Cabp4<tm1.1(KOMP)Vlcg>/Cabp4<tm1.1(KOMP)Vlcg>	C57BL/6N-Cabp4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797409	F	MP:0002941	increased circulating alanine transaminase level	Cacybp<tm1b(EUCOMM)Wtsi>/Cacybp<+>	C57BL/6N-Cacybp<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797409	M	MP:0000219	increased neutrophil cell number	Cacybp<tm1b(EUCOMM)Wtsi>/Cacybp<+>	C57BL/6N-Cacybp<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797410	M	MP:0000274	enlarged heart	Calhm1<tm1.1(KOMP)Vlcg>/Calhm1<tm1.1(KOMP)Vlcg>	C57BL/6N-Calhm1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797410	M	MP:0000266	abnormal heart morphology	Calhm1<tm1.1(KOMP)Vlcg>/Calhm1<tm1.1(KOMP)Vlcg>	C57BL/6N-Calhm1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797411	M	MP:0005293	impaired glucose tolerance	Capn11<tm1b(EUCOMM)Wtsi>/Capn11<tm1b(EUCOMM)Wtsi>	C57BL/6N-Capn11<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797412	M	MP:0010378	increased respiratory quotient	Caskin1<tm1b(KOMP)Wtsi>/Caskin1<+>	C57BL/6N-Caskin1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797412	M	MP:0002631	abnormal epididymis morphology	Caskin1<tm1b(KOMP)Wtsi>/Caskin1<+>	C57BL/6N-Caskin1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797412	M	MP:0011625	cystolithiasis	Caskin1<tm1b(KOMP)Wtsi>/Caskin1<+>	C57BL/6N-Caskin1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797412	F	MP:0002075	abnormal coat/hair pigmentation	Caskin1<tm1b(KOMP)Wtsi>/Caskin1<+>	C57BL/6N-Caskin1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797412	M	MP:0000538	abnormal urinary bladder morphology	Caskin1<tm1b(KOMP)Wtsi>/Caskin1<+>	C57BL/6N-Caskin1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797413	M	MP:0005554	decreased circulating creatinine level	Casq1<tm1b(EUCOMM)Wtsi>/Casq1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Casq1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797413	F	MP:0020420	abnormal freezing behavior	Casq1<tm1b(EUCOMM)Wtsi>/Casq1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Casq1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797413	F	MP:0005568	increased circulating total protein level	Casq1<tm1b(EUCOMM)Wtsi>/Casq1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Casq1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797413	M	MP:0010053	decreased grip strength	Casq1<tm1b(EUCOMM)Wtsi>/Casq1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Casq1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797413	F	MP:0005278	abnormal cholesterol homeostasis	Casq1<tm1b(EUCOMM)Wtsi>/Casq1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Casq1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797414	M	MP:0001925	male infertility	Catsper3<tm1.1(KOMP)Vlcg>/Catsper3<tm1.1(KOMP)Vlcg>	C57BL/6N-Catsper3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797416	F	MP:0001417	decreased exploration in new environment	Ccdc124<tm1b(KOMP)Wtsi>/Ccdc124<tm1b(KOMP)Wtsi>	C57BL/6N-Ccdc124<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797416	F	MP:0001399	hyperactivity	Ccdc124<tm1b(KOMP)Wtsi>/Ccdc124<tm1b(KOMP)Wtsi>	C57BL/6N-Ccdc124<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797417	M	MP:0003960	increased lean body mass	Ccdc127<tm1b(EUCOMM)Wtsi>/Ccdc127<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ccdc127<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797417	F	MP:0000218	increased leukocyte cell number	Ccdc127<tm1b(EUCOMM)Wtsi>/Ccdc127<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ccdc127<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797420	M	MP:0001556	increased circulating HDL cholesterol level	Ccl9<tm1(KOMP)Vlcg>/Ccl9<tm1(KOMP)Vlcg>	C57BL/6N-Ccl9<tm1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797420	M	MP:0000274	enlarged heart	Ccl9<tm1(KOMP)Vlcg>/Ccl9<tm1(KOMP)Vlcg>	C57BL/6N-Ccl9<tm1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797420	M	MP:0000266	abnormal heart morphology	Ccl9<tm1(KOMP)Vlcg>/Ccl9<tm1(KOMP)Vlcg>	C57BL/6N-Ccl9<tm1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797420	M	MP:0005178	increased circulating cholesterol level	Ccl9<tm1(KOMP)Vlcg>/Ccl9<tm1(KOMP)Vlcg>	C57BL/6N-Ccl9<tm1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797422	F	MP:0000274	enlarged heart	Cd300e<tm1.1(KOMP)Vlcg>/Cd300e<tm1.1(KOMP)Vlcg>	C57BL/6N-Cd300e<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797422	M	MP:0002631	abnormal epididymis morphology	Cd300e<tm1.1(KOMP)Vlcg>/Cd300e<tm1.1(KOMP)Vlcg>	C57BL/6N-Cd300e<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797422	M	MP:0004931	enlarged epididymis	Cd300e<tm1.1(KOMP)Vlcg>/Cd300e<tm1.1(KOMP)Vlcg>	C57BL/6N-Cd300e<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797424	F	MP:0001120	abnormal uterus morphology	Cd5<tm1.1(KOMP)Mbp>/Cd5<tm1.1(KOMP)Mbp>	C57BL/6N-Cd5<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5797424	M	MP:0004952	increased spleen weight	Cd5<tm1.1(KOMP)Mbp>/Cd5<tm1.1(KOMP)Mbp>	C57BL/6N-Cd5<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5797424	F	MP:0002060	abnormal skin morphology	Cd5<tm1.1(KOMP)Mbp>/Cd5<tm1.1(KOMP)Mbp>	C57BL/6N-Cd5<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5797424	F	MP:0000691	enlarged spleen	Cd5<tm1.1(KOMP)Mbp>/Cd5<tm1.1(KOMP)Mbp>	C57BL/6N-Cd5<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5797424	F	MP:0000689	abnormal spleen morphology	Cd5<tm1.1(KOMP)Mbp>/Cd5<tm1.1(KOMP)Mbp>	C57BL/6N-Cd5<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5797425	M	MP:0005599	increased cardiac muscle contractility	Cdc26<tm1b(EUCOMM)Hmgu>/Cdc26<+>	C57BL/6N-Cdc26<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5797426	M	MP:0003961	decreased lean body mass	Cdh19<tm1a(EUCOMM)Wtsi>/Cdh19<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cdh19<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797426	M	MP:0010124	decreased bone mineral content	Cdh19<tm1a(EUCOMM)Wtsi>/Cdh19<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cdh19<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797427	M	MP:0002590	increased mean corpuscular volume	Cdk4<tm1b(NCOM)Mfgc>/Cdk4<+>	C57BL/6N-Cdk4<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797427	F	MP:0001258	decreased body length	Cdk4<tm1b(NCOM)Mfgc>/Cdk4<+>	C57BL/6N-Cdk4<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797428	M	MP:0001925	male infertility	Cdk4<tm1b(NCOM)Mfgc>/Cdk4<tm1b(NCOM)Mfgc>	C57BL/6N-Cdk4<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797428	F	MP:0001926	female infertility	Cdk4<tm1b(NCOM)Mfgc>/Cdk4<tm1b(NCOM)Mfgc>	C57BL/6N-Cdk4<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797428	M	MP:0001697	abnormal embryo size	Cdk4<tm1b(NCOM)Mfgc>/Cdk4<tm1b(NCOM)Mfgc>	C57BL/6N-Cdk4<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797428	M	MP:0001297	microphthalmia	Cdk4<tm1b(NCOM)Mfgc>/Cdk4<tm1b(NCOM)Mfgc>	C57BL/6N-Cdk4<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797430	M	MP:0000266	abnormal heart morphology	Cdk9<tm1.1(KOMP)Vlcg>/Cdk9<+>	C57BL/6N-Cdk9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797430	F	MP:0002574	increased vertical activity	Cdk9<tm1.1(KOMP)Vlcg>/Cdk9<+>	C57BL/6N-Cdk9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797430	M	MP:0000274	enlarged heart	Cdk9<tm1.1(KOMP)Vlcg>/Cdk9<+>	C57BL/6N-Cdk9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797430	M	MP:0004931	enlarged epididymis	Cdk9<tm1.1(KOMP)Vlcg>/Cdk9<+>	C57BL/6N-Cdk9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797430	M	MP:0002631	abnormal epididymis morphology	Cdk9<tm1.1(KOMP)Vlcg>/Cdk9<+>	C57BL/6N-Cdk9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797432	F	MP:0000702	enlarged lymph nodes	Cecr2<tm2b(EUCOMM)Hmgu>/Cecr2<+>	C57BL/6N-Cecr2<tm2b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5797432	F	MP:0001417	decreased exploration in new environment	Cecr2<tm2b(EUCOMM)Hmgu>/Cecr2<+>	C57BL/6N-Cecr2<tm2b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5797432	F	MP:0004156	abnormal QT variability	Cecr2<tm2b(EUCOMM)Hmgu>/Cecr2<+>	C57BL/6N-Cecr2<tm2b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5797433	M	MP:0005179	decreased circulating cholesterol level	Celf4<tm1a(EUCOMM)Wtsi>/Celf4<+>	C57BL/6N-Celf4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797433	M	MP:0000195	decreased circulating calcium level	Celf4<tm1a(EUCOMM)Wtsi>/Celf4<+>	C57BL/6N-Celf4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797433	F	MP:0002079	increased circulating insulin level	Celf4<tm1a(EUCOMM)Wtsi>/Celf4<+>	C57BL/6N-Celf4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797433	F	MP:0005293	impaired glucose tolerance	Celf4<tm1a(EUCOMM)Wtsi>/Celf4<+>	C57BL/6N-Celf4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797435	M	MP:0005505	thrombocytosis	Ces2f<tm1b(KOMP)Wtsi>/Ces2f<tm1b(KOMP)Wtsi>	C57BL/6N-Ces2f<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797435	M	MP:0010067	increased red blood cell distribution width	Ces2f<tm1b(KOMP)Wtsi>/Ces2f<tm1b(KOMP)Wtsi>	C57BL/6N-Ces2f<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797436	M	MP:0005565	increased blood urea nitrogen level	Cfap61<tm2a(EUCOMM)Wtsi>/Cfap61<tm2a(EUCOMM)Wtsi>	C57BL/6N-Cfap61<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797436	F	MP:0010124	decreased bone mineral content	Cfap61<tm2a(EUCOMM)Wtsi>/Cfap61<tm2a(EUCOMM)Wtsi>	C57BL/6N-Cfap61<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797436	M	MP:0001925	male infertility	Cfap61<tm2a(EUCOMM)Wtsi>/Cfap61<tm2a(EUCOMM)Wtsi>	C57BL/6N-Cfap61<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797441	M	MP:0010024	increased total body fat amount	Cmpk2<tm1b(KOMP)Wtsi>/Cmpk2<tm1b(KOMP)Wtsi>	C57BL/6N-Cmpk2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797441	M	MP:0010124	decreased bone mineral content	Cmpk2<tm1b(KOMP)Wtsi>/Cmpk2<tm1b(KOMP)Wtsi>	C57BL/6N-Cmpk2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797441	M	MP:0005178	increased circulating cholesterol level	Cmpk2<tm1b(KOMP)Wtsi>/Cmpk2<tm1b(KOMP)Wtsi>	C57BL/6N-Cmpk2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797441	F	MP:0001402	decreased locomotor activity	Cmpk2<tm1b(KOMP)Wtsi>/Cmpk2<tm1b(KOMP)Wtsi>	C57BL/6N-Cmpk2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797441	M	MP:0002590	increased mean corpuscular volume	Cmpk2<tm1b(KOMP)Wtsi>/Cmpk2<tm1b(KOMP)Wtsi>	C57BL/6N-Cmpk2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797442	M	MP:0012768	decreased KLRG1-positive NK cell number	Cnot4<tm1b(EUCOMM)Wtsi>/Cnot4<+>	C57BL/6N-Cnot4<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797442	F	MP:0003961	decreased lean body mass	Cnot4<tm1b(EUCOMM)Wtsi>/Cnot4<+>	C57BL/6N-Cnot4<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797442	F	MP:0010024	increased total body fat amount	Cnot4<tm1b(EUCOMM)Wtsi>/Cnot4<+>	C57BL/6N-Cnot4<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797442	F	MP:0003795	abnormal bone structure	Cnot4<tm1b(EUCOMM)Wtsi>/Cnot4<+>	C57BL/6N-Cnot4<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797442	M	MP:0002966	decreased circulating alkaline phosphatase level	Cnot4<tm1b(EUCOMM)Wtsi>/Cnot4<+>	C57BL/6N-Cnot4<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797442	F	MP:0010124	decreased bone mineral content	Cnot4<tm1b(EUCOMM)Wtsi>/Cnot4<+>	C57BL/6N-Cnot4<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797443	M	MP:0005419	decreased circulating serum albumin level	Cnpy1<tm1(KOMP)Wtsi>/Cnpy1<tm1(KOMP)Wtsi>	C57BL/6N-Cnpy1<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797444	F	MP:0002941	increased circulating alanine transaminase level	Cox15<tm1.1(KOMP)Vlcg>/Cox15<+>	C57BL/6N-Cox15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797444	M	MP:0002833	increased heart weight	Cox15<tm1.1(KOMP)Vlcg>/Cox15<+>	C57BL/6N-Cox15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797444	M	MP:0008725	increased heart atrium size	Cox15<tm1.1(KOMP)Vlcg>/Cox15<+>	C57BL/6N-Cox15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797444	M	MP:0000266	abnormal heart morphology	Cox15<tm1.1(KOMP)Vlcg>/Cox15<+>	C57BL/6N-Cox15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797444	F	MP:0005343	increased circulating aspartate transaminase level	Cox15<tm1.1(KOMP)Vlcg>/Cox15<+>	C57BL/6N-Cox15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797445	M	MP:0001289	persistence of hyaloid vascular system	Cox5b<tm2b(EUCOMM)Hmgu>/Cox5b<+>	C57BL/6N-Cox5b<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5797446	M	MP:0011110	preweaning lethality, incomplete penetrance	Cpa3<tm1.1(KOMP)Vlcg>/Cpa3<tm1.1(KOMP)Vlcg>	C57BL/6N-Cpa3<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797446	M	MP:0002135	abnormal kidney morphology	Cpa3<tm1.1(KOMP)Vlcg>/Cpa3<tm1.1(KOMP)Vlcg>	C57BL/6N-Cpa3<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797447	M	MP:0010024	increased total body fat amount	Cpt1c<tm1b(EUCOMM)Wtsi>/Cpt1c<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cpt1c<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797447	F	MP:0010124	decreased bone mineral content	Cpt1c<tm1b(EUCOMM)Wtsi>/Cpt1c<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cpt1c<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797447	F	MP:0001120	abnormal uterus morphology	Cpt1c<tm1b(EUCOMM)Wtsi>/Cpt1c<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cpt1c<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797447	M	MP:0002175	decreased brain weight	Cpt1c<tm1b(EUCOMM)Wtsi>/Cpt1c<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cpt1c<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797448	M	MP:0000266	abnormal heart morphology	Crbn<tm1b(KOMP)Wtsi>/Crbn<tm1b(KOMP)Wtsi>	C57BL/6N-Crbn<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797448	F	MP:0001333	absent optic nerve	Crbn<tm1b(KOMP)Wtsi>/Crbn<tm1b(KOMP)Wtsi>	C57BL/6N-Crbn<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797448	F	MP:0002092	abnormal eye morphology	Crbn<tm1b(KOMP)Wtsi>/Crbn<tm1b(KOMP)Wtsi>	C57BL/6N-Crbn<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797448	M	MP:0000494	abnormal cecum morphology	Crbn<tm1b(KOMP)Wtsi>/Crbn<tm1b(KOMP)Wtsi>	C57BL/6N-Crbn<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797448	F	MP:0009142	decreased prepulse inhibition	Crbn<tm1b(KOMP)Wtsi>/Crbn<tm1b(KOMP)Wtsi>	C57BL/6N-Crbn<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797448	M	MP:0000274	enlarged heart	Crbn<tm1b(KOMP)Wtsi>/Crbn<tm1b(KOMP)Wtsi>	C57BL/6N-Crbn<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797450	M	MP:0002631	abnormal epididymis morphology	Crybb3<tm1.1(KOMP)Vlcg>/Crybb3<tm1.1(KOMP)Vlcg>	C57BL/6N-Crybb3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797450	M	MP:0004931	enlarged epididymis	Crybb3<tm1.1(KOMP)Vlcg>/Crybb3<tm1.1(KOMP)Vlcg>	C57BL/6N-Crybb3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797451	M	MP:0000438	abnormal cranium morphology	Csnk1g3<tm1a(EUCOMM)Wtsi>/Csnk1g3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Csnk1g3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797451	M	MP:0002875	decreased erythrocyte cell number	Csnk1g3<tm1a(EUCOMM)Wtsi>/Csnk1g3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Csnk1g3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797451	F	MP:0010124	decreased bone mineral content	Csnk1g3<tm1a(EUCOMM)Wtsi>/Csnk1g3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Csnk1g3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797451	F	MP:0001258	decreased body length	Csnk1g3<tm1a(EUCOMM)Wtsi>/Csnk1g3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Csnk1g3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797451	M	MP:0000182	increased circulating LDL cholesterol level	Csnk1g3<tm1a(EUCOMM)Wtsi>/Csnk1g3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Csnk1g3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797451	F	MP:0002966	decreased circulating alkaline phosphatase level	Csnk1g3<tm1a(EUCOMM)Wtsi>/Csnk1g3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Csnk1g3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797452	M	MP:0004931	enlarged epididymis	Cst9<tm1.1(KOMP)Vlcg>/Cst9<tm1.1(KOMP)Vlcg>	C57BL/6N-Cst9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797452	M	MP:0002631	abnormal epididymis morphology	Cst9<tm1.1(KOMP)Vlcg>/Cst9<tm1.1(KOMP)Vlcg>	C57BL/6N-Cst9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797453	F	MP:0001399	hyperactivity	Ctdsp1<tm1b(EUCOMM)Wtsi>/Ctdsp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ctdsp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797453	M	MP:0010053	decreased grip strength	Ctdsp1<tm1b(EUCOMM)Wtsi>/Ctdsp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ctdsp1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797455	F	MP:0001289	persistence of hyaloid vascular system	Cth<tm1b(EUCOMM)Hmgu>/Cth<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cth<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797455	M	MP:0001303	abnormal lens morphology	Cth<tm1b(EUCOMM)Hmgu>/Cth<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cth<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797458	F	MP:0005505	thrombocytosis	Ctnnbip1<tm1b(EUCOMM)Wtsi>/Ctnnbip1<+>	C57BL/6N-Ctnnbip1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797458	M	MP:0000274	enlarged heart	Ctnnbip1<tm1b(EUCOMM)Wtsi>/Ctnnbip1<+>	C57BL/6N-Ctnnbip1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797460	M	MP:0010124	decreased bone mineral content	Cxcr1<tm1a(EUCOMM)Wtsi>/Cxcr1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797460	M	MP:0001258	decreased body length	Cxcr1<tm1a(EUCOMM)Wtsi>/Cxcr1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797460	M	MP:0002079	increased circulating insulin level	Cxcr1<tm1a(EUCOMM)Wtsi>/Cxcr1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797460	M	MP:0013279	increased fasting circulating glucose level	Cxcr1<tm1a(EUCOMM)Wtsi>/Cxcr1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cxcr1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797461	M	MP:0013279	increased fasting circulating glucose level	Cyb561a3<tm2b(EUCOMM)Hmgu>/Cyb561a3<tm2b(EUCOMM)Hmgu>	C57BL/6N-Cyb561a3<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797462	M	MP:0001146	abnormal testis morphology	Cygb<tm1b(EUCOMM)Wtsi>/Cygb<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cygb<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797462	M	MP:0002833	increased heart weight	Cygb<tm1b(EUCOMM)Wtsi>/Cygb<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cygb<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797462	M	MP:0010025	decreased total body fat amount	Cygb<tm1b(EUCOMM)Wtsi>/Cygb<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cygb<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797462	M	MP:0010123	increased bone mineral content	Cygb<tm1b(EUCOMM)Wtsi>/Cygb<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cygb<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797462	M	MP:0003960	increased lean body mass	Cygb<tm1b(EUCOMM)Wtsi>/Cygb<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cygb<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797462	M	MP:0001147	small testis	Cygb<tm1b(EUCOMM)Wtsi>/Cygb<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cygb<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797463	F	MP:0000274	enlarged heart	Cyp27a1<tm1.1(KOMP)Vlcg>/Cyp27a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Cyp27a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797463	F	MP:0000266	abnormal heart morphology	Cyp27a1<tm1.1(KOMP)Vlcg>/Cyp27a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Cyp27a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797463	M	MP:0002644	decreased circulating triglyceride level	Cyp27a1<tm1.1(KOMP)Vlcg>/Cyp27a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Cyp27a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797463	M	MP:0002981	increased liver weight	Cyp27a1<tm1.1(KOMP)Vlcg>/Cyp27a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Cyp27a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797463	M	MP:0005419	decreased circulating serum albumin level	Cyp27a1<tm1.1(KOMP)Vlcg>/Cyp27a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Cyp27a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797463	M	MP:0005179	decreased circulating cholesterol level	Cyp27a1<tm1.1(KOMP)Vlcg>/Cyp27a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Cyp27a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797463	F	MP:0010393	shortened QRS complex duration	Cyp27a1<tm1.1(KOMP)Vlcg>/Cyp27a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Cyp27a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797466	M	MP:0000219	increased neutrophil cell number	Dcc<tm1b(NCOM)Mfgc>/Dcc<+>	C57BL/6N-Dcc<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797468	F	MP:0010052	increased grip strength	Dclk1<tm1a(EUCOMM)Wtsi>/Dclk1<+>	C57BL/6N-Dclk1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797470	F	MP:0005477	increased circulating thyroxine level	Ddx42<tm1b(EUCOMM)Wtsi>/Ddx42<+>	C57BL/6N-Ddx42<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797471	M	MP:0000274	enlarged heart	Ddx54<tm1.1(KOMP)Vlcg>/Ddx54<+>	C57BL/6N-Ddx54<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797472	M	MP:0001510	abnormal coat appearance	Ddx55<tm1a(EUCOMM)Wtsi>/Ddx55<+>	C57BL/6N-Ddx55<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797472	M	MP:0010067	increased red blood cell distribution width	Ddx55<tm1a(EUCOMM)Wtsi>/Ddx55<+>	C57BL/6N-Ddx55<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797473	M	MP:0011625	cystolithiasis	Dennd2c<tm1b(KOMP)Wtsi>/Dennd2c<tm1b(KOMP)Wtsi>	C57BL/6N-Dennd2c<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797473	M	MP:0000538	abnormal urinary bladder morphology	Dennd2c<tm1b(KOMP)Wtsi>/Dennd2c<tm1b(KOMP)Wtsi>	C57BL/6N-Dennd2c<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797476	M	MP:0003961	decreased lean body mass	Dhx29<tm1.1(KOMP)Vlcg>/Dhx29<+>	C57BL/6N-Dhx29<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797477	F	MP:0005477	increased circulating thyroxine level	Dhx33<tm1b(KOMP)Wtsi>/Dhx33<+>	C57BL/6N-Dhx33<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797478	M	MP:0011110	preweaning lethality, incomplete penetrance	Dkk4<tm1.1(KOMP)Vlcg>/Dkk4<tm1.1(KOMP)Vlcg>	C57BL/6N-Dkk4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797478	F	MP:0000274	enlarged heart	Dkk4<tm1.1(KOMP)Vlcg>/Dkk4<tm1.1(KOMP)Vlcg>	C57BL/6N-Dkk4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797478	F	MP:0000266	abnormal heart morphology	Dkk4<tm1.1(KOMP)Vlcg>/Dkk4<tm1.1(KOMP)Vlcg>	C57BL/6N-Dkk4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797479	M	MP:0002941	increased circulating alanine transaminase level	Dlec1<tm1b(EUCOMM)Wtsi>/Dlec1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dlec1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5797479	M	MP:0001925	male infertility	Dlec1<tm1b(EUCOMM)Wtsi>/Dlec1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dlec1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5797480	M	MP:0001891	hydrocephaly	Dlg5<tm1b(EUCOMM)Wtsi>/Dlg5<+>	C57BL/6N-Dlg5<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797480	M	MP:0002152	abnormal brain morphology	Dlg5<tm1b(EUCOMM)Wtsi>/Dlg5<+>	C57BL/6N-Dlg5<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797481	F	MP:0013279	increased fasting circulating glucose level	Dnaja4<tm1b(KOMP)Wtsi>/Dnaja4<tm1b(KOMP)Wtsi>	C57BL/6N-Dnaja4<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797481	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Dnaja4<tm1b(KOMP)Wtsi>/Dnaja4<tm1b(KOMP)Wtsi>	C57BL/6N-Dnaja4<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797485	M	MP:0001258	decreased body length	Dok7<tm1.1(KOMP)Vlcg>/Dok7<+>	C57BL/6N-Dok7<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797485	M	MP:0000219	increased neutrophil cell number	Dok7<tm1.1(KOMP)Vlcg>/Dok7<+>	C57BL/6N-Dok7<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797485	M	MP:0005016	decreased lymphocyte cell number	Dok7<tm1.1(KOMP)Vlcg>/Dok7<+>	C57BL/6N-Dok7<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797486	M	MP:0001146	abnormal testis morphology	Aoc1l1<tm1.1(KOMP)Vlcg>/Aoc1l1<tm1.1(KOMP)Vlcg>	C57BL/6N-Aoc1l1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797486	M	MP:0001147	small testis	Aoc1l1<tm1.1(KOMP)Vlcg>/Aoc1l1<tm1.1(KOMP)Vlcg>	C57BL/6N-Aoc1l1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797486	M	MP:0000274	enlarged heart	Aoc1l1<tm1.1(KOMP)Vlcg>/Aoc1l1<tm1.1(KOMP)Vlcg>	C57BL/6N-Aoc1l1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797486	F	MP:0011110	preweaning lethality, incomplete penetrance	Aoc1l1<tm1.1(KOMP)Vlcg>/Aoc1l1<tm1.1(KOMP)Vlcg>	C57BL/6N-Aoc1l1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797486	M	MP:0000266	abnormal heart morphology	Aoc1l1<tm1.1(KOMP)Vlcg>/Aoc1l1<tm1.1(KOMP)Vlcg>	C57BL/6N-Aoc1l1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797487	M	MP:0002135	abnormal kidney morphology	Dpf2<tm1b(EUCOMM)Hmgu>/Dpf2<+>	C57BL/6N-Dpf2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5797487	M	MP:0002059	abnormal seminal vesicle morphology	Dpf2<tm1b(EUCOMM)Hmgu>/Dpf2<+>	C57BL/6N-Dpf2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5797493	M	MP:0010053	decreased grip strength	Dtl<tm1b(EUCOMM)Wtsi>/Dtl<+>	C57BL/6N-Dtl<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5797494	M	MP:0001489	decreased startle reflex	Dyrk1b<tm1b(EUCOMM)Wtsi>/Dyrk1b<+>	C57BL/6N-Dyrk1b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797494	M	MP:0000063	decreased bone mineral density	Dyrk1b<tm1b(EUCOMM)Wtsi>/Dyrk1b<+>	C57BL/6N-Dyrk1b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797494	F	MP:0003733	abnormal retina inner nuclear layer morphology	Dyrk1b<tm1b(EUCOMM)Wtsi>/Dyrk1b<+>	C57BL/6N-Dyrk1b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797495	F	MP:0000274	enlarged heart	Edar<tm1b(KOMP)Wtsi>/Edar<+>	C57BL/6N-Edar<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797495	F	MP:0009142	decreased prepulse inhibition	Edar<tm1b(KOMP)Wtsi>/Edar<+>	C57BL/6N-Edar<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797496	M	MP:0005102	abnormal iris pigmentation	Eddm3b<tm1b(KOMP)Wtsi>/Eddm3b<tm1b(KOMP)Wtsi>	C57BL/6N-Eddm3b<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797496	M	MP:0005011	increased eosinophil cell number	Eddm3b<tm1b(KOMP)Wtsi>/Eddm3b<tm1b(KOMP)Wtsi>	C57BL/6N-Eddm3b<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797496	M	MP:0002753	dilated heart left ventricle	Eddm3b<tm1b(KOMP)Wtsi>/Eddm3b<tm1b(KOMP)Wtsi>	C57BL/6N-Eddm3b<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797496	M	MP:0002606	increased basophil cell number	Eddm3b<tm1b(KOMP)Wtsi>/Eddm3b<tm1b(KOMP)Wtsi>	C57BL/6N-Eddm3b<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797498	M	MP:0001488	increased startle reflex	Eftud2<tm1b(KOMP)Wtsi>/Eftud2<+>	C57BL/6N-Eftud2<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797498	F	MP:0000221	decreased leukocyte cell number	Eftud2<tm1b(KOMP)Wtsi>/Eftud2<+>	C57BL/6N-Eftud2<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797498	M	MP:0001489	decreased startle reflex	Eftud2<tm1b(KOMP)Wtsi>/Eftud2<+>	C57BL/6N-Eftud2<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797498	M	MP:0001417	decreased exploration in new environment	Eftud2<tm1b(KOMP)Wtsi>/Eftud2<+>	C57BL/6N-Eftud2<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797498	F	MP:0005016	decreased lymphocyte cell number	Eftud2<tm1b(KOMP)Wtsi>/Eftud2<+>	C57BL/6N-Eftud2<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797498	F	MP:0010579	increased heart left ventricle size	Eftud2<tm1b(KOMP)Wtsi>/Eftud2<+>	C57BL/6N-Eftud2<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797498	M	MP:0005505	thrombocytosis	Eftud2<tm1b(KOMP)Wtsi>/Eftud2<+>	C57BL/6N-Eftud2<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797499	M	MP:0002631	abnormal epididymis morphology	Egfl8<tm1.1(KOMP)Vlcg>/Egfl8<tm1.1(KOMP)Vlcg>	C57BL/6N-Egfl8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797499	M	MP:0004931	enlarged epididymis	Egfl8<tm1.1(KOMP)Vlcg>/Egfl8<tm1.1(KOMP)Vlcg>	C57BL/6N-Egfl8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797499	F	MP:0001399	hyperactivity	Egfl8<tm1.1(KOMP)Vlcg>/Egfl8<tm1.1(KOMP)Vlcg>	C57BL/6N-Egfl8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797499	M	MP:0001891	hydrocephaly	Egfl8<tm1.1(KOMP)Vlcg>/Egfl8<tm1.1(KOMP)Vlcg>	C57BL/6N-Egfl8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797499	M	MP:0002152	abnormal brain morphology	Egfl8<tm1.1(KOMP)Vlcg>/Egfl8<tm1.1(KOMP)Vlcg>	C57BL/6N-Egfl8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797500	F	MP:0001258	decreased body length	Egr1<tm1b(NCOM)Mfgc>/Egr1<+>	C57BL/6N-Egr1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797500	F	MP:0005013	increased lymphocyte cell number	Egr1<tm1b(NCOM)Mfgc>/Egr1<+>	C57BL/6N-Egr1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797501	F	MP:0002637	small uterus	Egr1<tm1b(NCOM)Mfgc>/Egr1<tm1b(NCOM)Mfgc>	C57BL/6N-Egr1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797501	F	MP:0008259	abnormal optic disk morphology	Egr1<tm1b(NCOM)Mfgc>/Egr1<tm1b(NCOM)Mfgc>	C57BL/6N-Egr1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797501	M	MP:0001925	male infertility	Egr1<tm1b(NCOM)Mfgc>/Egr1<tm1b(NCOM)Mfgc>	C57BL/6N-Egr1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797501	M	MP:0003642	absent seminal vesicle	Egr1<tm1b(NCOM)Mfgc>/Egr1<tm1b(NCOM)Mfgc>	C57BL/6N-Egr1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797501	F	MP:0001926	female infertility	Egr1<tm1b(NCOM)Mfgc>/Egr1<tm1b(NCOM)Mfgc>	C57BL/6N-Egr1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797503	M	MP:0001314	cornea opacity	Elmo3<tm1.1(KOMP)Vlcg>/Elmo3<tm1.1(KOMP)Vlcg>	C57BL/6N-Elmo3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797504	M	MP:0001556	increased circulating HDL cholesterol level	Elmod2<tm1b(EUCOMM)Hmgu>/Elmod2<+>	C57BL/6N-Elmod2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797504	M	MP:0003961	decreased lean body mass	Elmod2<tm1b(EUCOMM)Hmgu>/Elmod2<+>	C57BL/6N-Elmod2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797504	M	MP:0010024	increased total body fat amount	Elmod2<tm1b(EUCOMM)Hmgu>/Elmod2<+>	C57BL/6N-Elmod2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797504	M	MP:0001406	abnormal gait	Elmod2<tm1b(EUCOMM)Hmgu>/Elmod2<+>	C57BL/6N-Elmod2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797504	M	MP:0010124	decreased bone mineral content	Elmod2<tm1b(EUCOMM)Hmgu>/Elmod2<+>	C57BL/6N-Elmod2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797504	M	MP:0005178	increased circulating cholesterol level	Elmod2<tm1b(EUCOMM)Hmgu>/Elmod2<+>	C57BL/6N-Elmod2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797504	M	MP:0005564	increased hemoglobin content	Elmod2<tm1b(EUCOMM)Hmgu>/Elmod2<+>	C57BL/6N-Elmod2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797505	M	MP:0001417	decreased exploration in new environment	Elmod2<tm1b(EUCOMM)Hmgu>/Elmod2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elmod2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797506	F	MP:0010024	increased total body fat amount	Emc8<tm1b(EUCOMM)Hmgu>/Emc8<+>	C57BL/6N-Emc8<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797506	F	MP:0003961	decreased lean body mass	Emc8<tm1b(EUCOMM)Hmgu>/Emc8<+>	C57BL/6N-Emc8<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797506	M	MP:0010067	increased red blood cell distribution width	Emc8<tm1b(EUCOMM)Hmgu>/Emc8<+>	C57BL/6N-Emc8<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797506	M	MP:0000274	enlarged heart	Emc8<tm1b(EUCOMM)Hmgu>/Emc8<+>	C57BL/6N-Emc8<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797506	M	MP:0002546	mydriasis	Emc8<tm1b(EUCOMM)Hmgu>/Emc8<+>	C57BL/6N-Emc8<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797506	M	MP:0000219	increased neutrophil cell number	Emc8<tm1b(EUCOMM)Hmgu>/Emc8<+>	C57BL/6N-Emc8<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797506	M	MP:0010097	abnormal retina blood vessel morphology	Emc8<tm1b(EUCOMM)Hmgu>/Emc8<+>	C57BL/6N-Emc8<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797509	M	MP:0010024	increased total body fat amount	Enox1<tm1.1(KOMP)Vlcg>/Enox1<+>	C57BL/6N-Enox1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797509	F	MP:0000208	decreased hematocrit	Enox1<tm1.1(KOMP)Vlcg>/Enox1<+>	C57BL/6N-Enox1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797509	M	MP:0011954	shortened PQ interval	Enox1<tm1.1(KOMP)Vlcg>/Enox1<+>	C57BL/6N-Enox1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797510	M	MP:0000274	enlarged heart	Entpd8<tm1.1(KOMP)Vlcg>/Entpd8<tm1.1(KOMP)Vlcg>	C57BL/6N-Entpd8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797510	M	MP:0000266	abnormal heart morphology	Entpd8<tm1.1(KOMP)Vlcg>/Entpd8<tm1.1(KOMP)Vlcg>	C57BL/6N-Entpd8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797512	M	MP:0000219	increased neutrophil cell number	Epdr1<tm1b(NCOM)Mfgc>/Epdr1<tm1b(NCOM)Mfgc>	C57BL/6N-Epdr1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797512	F	MP:0002764	short tibia	Epdr1<tm1b(NCOM)Mfgc>/Epdr1<tm1b(NCOM)Mfgc>	C57BL/6N-Epdr1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797512	M	MP:0005016	decreased lymphocyte cell number	Epdr1<tm1b(NCOM)Mfgc>/Epdr1<tm1b(NCOM)Mfgc>	C57BL/6N-Epdr1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797513	F	MP:0001523	impaired righting response	Epha10<tm1.1(KOMP)Vlcg>/Epha10<tm1.1(KOMP)Vlcg>	C57BL/6N-Epha10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797514	M	MP:0000689	abnormal spleen morphology	Epha6<tm1b(KOMP)Wtsi>/Epha6<tm1b(KOMP)Wtsi>	C57BL/6N-Epha6<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797514	F	MP:0002060	abnormal skin morphology	Epha6<tm1b(KOMP)Wtsi>/Epha6<tm1b(KOMP)Wtsi>	C57BL/6N-Epha6<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797514	F	MP:0002135	abnormal kidney morphology	Epha6<tm1b(KOMP)Wtsi>/Epha6<tm1b(KOMP)Wtsi>	C57BL/6N-Epha6<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797514	M	MP:0000598	abnormal liver morphology	Epha6<tm1b(KOMP)Wtsi>/Epha6<tm1b(KOMP)Wtsi>	C57BL/6N-Epha6<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797514	M	MP:0002631	abnormal epididymis morphology	Epha6<tm1b(KOMP)Wtsi>/Epha6<tm1b(KOMP)Wtsi>	C57BL/6N-Epha6<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797514	M	MP:0004931	enlarged epididymis	Epha6<tm1b(KOMP)Wtsi>/Epha6<tm1b(KOMP)Wtsi>	C57BL/6N-Epha6<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797514	M	MP:0000599	enlarged liver	Epha6<tm1b(KOMP)Wtsi>/Epha6<tm1b(KOMP)Wtsi>	C57BL/6N-Epha6<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797515	M	MP:0005627	increased circulating potassium level	Ercc3<tm1b(NCOM)Mfgc>/Ercc3<+>	C57BL/6N-Ercc3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797515	M	MP:0009142	decreased prepulse inhibition	Ercc3<tm1b(NCOM)Mfgc>/Ercc3<+>	C57BL/6N-Ercc3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797515	F	MP:0005562	decreased mean corpuscular hemoglobin	Ercc3<tm1b(NCOM)Mfgc>/Ercc3<+>	C57BL/6N-Ercc3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797519	F	MP:0008935	decreased mean platelet volume	Ethe1<tm1b(EUCOMM)Wtsi>/Ethe1<+>	C57BL/6N-Ethe1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797521	F	MP:0013279	increased fasting circulating glucose level	Exosc3<tm1.1(KOMP)Vlcg>/Exosc3<+>	C57BL/6N-Exosc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797521	M	MP:0008528	polycystic kidney	Exosc3<tm1.1(KOMP)Vlcg>/Exosc3<+>	C57BL/6N-Exosc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797521	M	MP:0002135	abnormal kidney morphology	Exosc3<tm1.1(KOMP)Vlcg>/Exosc3<+>	C57BL/6N-Exosc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797523	M	MP:0010024	increased total body fat amount	F2<tm1b(EUCOMM)Hmgu>/F2<+>	C57BL/6N-F2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797523	M	MP:0003961	decreased lean body mass	F2<tm1b(EUCOMM)Hmgu>/F2<+>	C57BL/6N-F2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797523	M	MP:0010124	decreased bone mineral content	F2<tm1b(EUCOMM)Hmgu>/F2<+>	C57BL/6N-F2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797523	F	MP:0002965	increased circulating serum albumin level	F2<tm1b(EUCOMM)Hmgu>/F2<+>	C57BL/6N-F2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797523	F	MP:0010087	increased circulating fructosamine level	F2<tm1b(EUCOMM)Hmgu>/F2<+>	C57BL/6N-F2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797523	M	MP:0001417	decreased exploration in new environment	F2<tm1b(EUCOMM)Hmgu>/F2<+>	C57BL/6N-F2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797523	M	MP:0000745	tremors	F2<tm1b(EUCOMM)Hmgu>/F2<+>	C57BL/6N-F2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797524	M	MP:0002875	decreased erythrocyte cell number	Fhip1a<tm1b(EUCOMM)Wtsi>/Fhip1a<+>	C57BL/6N-Fhip1a1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797526	M	MP:0002590	increased mean corpuscular volume	Fam210a<tm1b(EUCOMM)Wtsi>/Fam210a<+>	C57BL/6N-Fam210a<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797529	M	MP:0010025	decreased total body fat amount	Dipk1a<tm1a(EUCOMM)Wtsi>/Dipk1a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dipk1a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797529	M	MP:0005633	increased circulating sodium level	Dipk1a<tm1a(EUCOMM)Wtsi>/Dipk1a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dipk1a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797529	M	MP:0003960	increased lean body mass	Dipk1a<tm1a(EUCOMM)Wtsi>/Dipk1a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dipk1a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797529	M	MP:0002833	increased heart weight	Dipk1a<tm1a(EUCOMM)Wtsi>/Dipk1a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Dipk1a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797530	M	MP:0002875	decreased erythrocyte cell number	Cibar1<tm1b(KOMP)Wtsi>/Cibar1<tm1b(KOMP)Wtsi>	C57BL/6N-Cibar1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797530	M	MP:0005292	improved glucose tolerance	Cibar1<tm1b(KOMP)Wtsi>/Cibar1<tm1b(KOMP)Wtsi>	C57BL/6N-Cibar1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797530	M	MP:0003442	decreased circulating glycerol level	Cibar1<tm1b(KOMP)Wtsi>/Cibar1<tm1b(KOMP)Wtsi>	C57BL/6N-Cibar1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797530	M	MP:0000221	decreased leukocyte cell number	Cibar1<tm1b(KOMP)Wtsi>/Cibar1<tm1b(KOMP)Wtsi>	C57BL/6N-Cibar1<tm1b(KOMP)Wtsi>/Wtsi	N	30395363
MGI:5797530	M	MP:0000221	decreased leukocyte cell number	Cibar1<tm1b(KOMP)Wtsi>/Cibar1<tm1b(KOMP)Wtsi>	C57BL/6N-Cibar1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797530	M	MP:0010025	decreased total body fat amount	Cibar1<tm1b(KOMP)Wtsi>/Cibar1<tm1b(KOMP)Wtsi>	C57BL/6N-Cibar1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797530	M	MP:0005449	abnormal food intake	Cibar1<tm1b(KOMP)Wtsi>/Cibar1<tm1b(KOMP)Wtsi>	C57BL/6N-Cibar1<tm1b(KOMP)Wtsi>/Wtsi	N	30395363
MGI:5797530	M	MP:0002874	decreased hemoglobin content	Cibar1<tm1b(KOMP)Wtsi>/Cibar1<tm1b(KOMP)Wtsi>	C57BL/6N-Cibar1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797530	M	MP:0000208	decreased hematocrit	Cibar1<tm1b(KOMP)Wtsi>/Cibar1<tm1b(KOMP)Wtsi>	C57BL/6N-Cibar1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797530	M	MP:0003960	increased lean body mass	Cibar1<tm1b(KOMP)Wtsi>/Cibar1<tm1b(KOMP)Wtsi>	C57BL/6N-Cibar1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797531	M	MP:0002875	decreased erythrocyte cell number	Fbxo11<tm2b(EUCOMM)Wtsi>/Fbxo11<+>	C57BL/6N-Fbxo11<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797531	M	MP:0000208	decreased hematocrit	Fbxo11<tm2b(EUCOMM)Wtsi>/Fbxo11<+>	C57BL/6N-Fbxo11<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797531	F	MP:0004151	decreased circulating iron level	Fbxo11<tm2b(EUCOMM)Wtsi>/Fbxo11<+>	C57BL/6N-Fbxo11<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797531	M	MP:0013279	increased fasting circulating glucose level	Fbxo11<tm2b(EUCOMM)Wtsi>/Fbxo11<+>	C57BL/6N-Fbxo11<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797531	M	MP:0005567	decreased circulating total protein level	Fbxo11<tm2b(EUCOMM)Wtsi>/Fbxo11<+>	C57BL/6N-Fbxo11<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797531	F	MP:0002764	short tibia	Fbxo11<tm2b(EUCOMM)Wtsi>/Fbxo11<+>	C57BL/6N-Fbxo11<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797531	M	MP:0010067	increased red blood cell distribution width	Fbxo11<tm2b(EUCOMM)Wtsi>/Fbxo11<+>	C57BL/6N-Fbxo11<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797532	F	MP:0002111	abnormal tail morphology	Fbxo22<tm1b(EUCOMM)Wtsi>/Fbxo22<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fbxo22<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5797532	F	MP:0001926	female infertility	Fbxo22<tm1b(EUCOMM)Wtsi>/Fbxo22<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fbxo22<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5797532	F	MP:0009142	decreased prepulse inhibition	Fbxo22<tm1b(EUCOMM)Wtsi>/Fbxo22<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fbxo22<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5797532	M	MP:0001925	male infertility	Fbxo22<tm1b(EUCOMM)Wtsi>/Fbxo22<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fbxo22<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5797532	F	MP:0010053	decreased grip strength	Fbxo22<tm1b(EUCOMM)Wtsi>/Fbxo22<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fbxo22<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5797533	F	MP:0002606	increased basophil cell number	Fbxo36<tm1b(KOMP)Wtsi>/Fbxo36<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo36<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797533	F	MP:0010053	decreased grip strength	Fbxo36<tm1b(KOMP)Wtsi>/Fbxo36<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo36<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797533	F	MP:0010067	increased red blood cell distribution width	Fbxo36<tm1b(KOMP)Wtsi>/Fbxo36<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo36<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797533	F	MP:0002953	thick ventricular wall	Fbxo36<tm1b(KOMP)Wtsi>/Fbxo36<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo36<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797533	F	MP:0000219	increased neutrophil cell number	Fbxo36<tm1b(KOMP)Wtsi>/Fbxo36<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo36<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797533	F	MP:0003921	abnormal heart left ventricle morphology	Fbxo36<tm1b(KOMP)Wtsi>/Fbxo36<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo36<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797534	F	MP:0010067	increased red blood cell distribution width	Fgb<tm1.1(KOMP)Vlcg>/Fgb<tm1.1(KOMP)Vlcg>	C57BL/6N-Fgb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797534	F	MP:0000274	enlarged heart	Fgb<tm1.1(KOMP)Vlcg>/Fgb<tm1.1(KOMP)Vlcg>	C57BL/6N-Fgb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797534	F	MP:0005293	impaired glucose tolerance	Fgb<tm1.1(KOMP)Vlcg>/Fgb<tm1.1(KOMP)Vlcg>	C57BL/6N-Fgb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797536	M	MP:0004258	abnormal placenta size	Fgf15<tm1.1(KOMP)Vlcg>/Fgf15<tm1.1(KOMP)Vlcg>	C57BL/6N-Fgf15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797538	M	MP:0009142	decreased prepulse inhibition	Fitm2<tm1.1(KOMP)Vlcg>/Fitm2<+>	C57BL/6N-Fitm2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797539	F	MP:0001120	abnormal uterus morphology	Fjx1<tm1.1(KOMP)Vlcg>/Fjx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fjx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797539	F	MP:0009709	hydrometra	Fjx1<tm1.1(KOMP)Vlcg>/Fjx1<tm1.1(KOMP)Vlcg>	C57BL/6N-Fjx1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797541	M	MP:0005178	increased circulating cholesterol level	Fndc7<tm1.1(KOMP)Vlcg>/Fndc7<tm1.1(KOMP)Vlcg>	C57BL/6N-Fndc7<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797541	M	MP:0005568	increased circulating total protein level	Fndc7<tm1.1(KOMP)Vlcg>/Fndc7<tm1.1(KOMP)Vlcg>	C57BL/6N-Fndc7<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797541	M	MP:0001556	increased circulating HDL cholesterol level	Fndc7<tm1.1(KOMP)Vlcg>/Fndc7<tm1.1(KOMP)Vlcg>	C57BL/6N-Fndc7<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797543	M	MP:0008725	increased heart atrium size	Folr1<tm1.1(KOMP)Vlcg>/Folr1<+>	C57BL/6N-Folr1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797543	M	MP:0001147	small testis	Folr1<tm1.1(KOMP)Vlcg>/Folr1<+>	C57BL/6N-Folr1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797543	F	MP:0005278	abnormal cholesterol homeostasis	Folr1<tm1.1(KOMP)Vlcg>/Folr1<+>	C57BL/6N-Folr1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797543	M	MP:0002135	abnormal kidney morphology	Folr1<tm1.1(KOMP)Vlcg>/Folr1<+>	C57BL/6N-Folr1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797545	M	MP:0001925	male infertility	Foxo4<tm1.1(KOMP)Vlcg>/Foxo4<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxo4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797547	F	MP:0000598	abnormal liver morphology	Fstl3<tm1.1(KOMP)Vlcg>/Fstl3<tm1.1(KOMP)Vlcg>	C57BL/6N-Fstl3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797547	F	MP:0000266	abnormal heart morphology	Fstl3<tm1.1(KOMP)Vlcg>/Fstl3<tm1.1(KOMP)Vlcg>	C57BL/6N-Fstl3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797547	M	MP:0001148	enlarged testis	Fstl3<tm1.1(KOMP)Vlcg>/Fstl3<tm1.1(KOMP)Vlcg>	C57BL/6N-Fstl3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797547	M	MP:0001146	abnormal testis morphology	Fstl3<tm1.1(KOMP)Vlcg>/Fstl3<tm1.1(KOMP)Vlcg>	C57BL/6N-Fstl3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797547	F	MP:0000274	enlarged heart	Fstl3<tm1.1(KOMP)Vlcg>/Fstl3<tm1.1(KOMP)Vlcg>	C57BL/6N-Fstl3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797548	F	MP:0001399	hyperactivity	Fzd2<tm1.1(KOMP)Vlcg>/Fzd2<+>	C57BL/6N-Fzd2<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5797549	M	MP:0000274	enlarged heart	Gabrr2<tm1b(KOMP)Wtsi>/Gabrr2<tm1b(KOMP)Wtsi>	C57BL/6N-Gabrr2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797549	M	MP:0001147	small testis	Gabrr2<tm1b(KOMP)Wtsi>/Gabrr2<tm1b(KOMP)Wtsi>	C57BL/6N-Gabrr2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797549	M	MP:0001146	abnormal testis morphology	Gabrr2<tm1b(KOMP)Wtsi>/Gabrr2<tm1b(KOMP)Wtsi>	C57BL/6N-Gabrr2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797549	M	MP:0000266	abnormal heart morphology	Gabrr2<tm1b(KOMP)Wtsi>/Gabrr2<tm1b(KOMP)Wtsi>	C57BL/6N-Gabrr2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797550	M	MP:0001325	abnormal retina morphology	Galk2<tm1b(EUCOMM)Hmgu>/Galk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Galk2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797550	M	MP:0002135	abnormal kidney morphology	Galk2<tm1b(EUCOMM)Hmgu>/Galk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Galk2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797550	M	MP:0002110	abnormal digit morphology	Galk2<tm1b(EUCOMM)Hmgu>/Galk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Galk2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797550	F	MP:0010052	increased grip strength	Galk2<tm1b(EUCOMM)Hmgu>/Galk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Galk2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797550	M	MP:0002792	abnormal retina vasculature morphology	Galk2<tm1b(EUCOMM)Hmgu>/Galk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Galk2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797550	F	MP:0003928	increased heart rate variability	Galk2<tm1b(EUCOMM)Hmgu>/Galk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Galk2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797550	F	MP:0005385	cardiovascular system phenotype	Galk2<tm1b(EUCOMM)Hmgu>/Galk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Galk2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797550	M	MP:0005344	increased circulating bilirubin level	Galk2<tm1b(EUCOMM)Hmgu>/Galk2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Galk2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797551	F	MP:0002060	abnormal skin morphology	Gas2l1<tm1.1(KOMP)Vlcg>/Gas2l1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gas2l1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797551	M	MP:0001147	small testis	Gas2l1<tm1.1(KOMP)Vlcg>/Gas2l1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gas2l1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797551	M	MP:0001925	male infertility	Gas2l1<tm1.1(KOMP)Vlcg>/Gas2l1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gas2l1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797551	M	MP:0001146	abnormal testis morphology	Gas2l1<tm1.1(KOMP)Vlcg>/Gas2l1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gas2l1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797552	F	MP:0000274	enlarged heart	Gas6<tm1.1(KOMP)Vlcg>/Gas6<tm1.1(KOMP)Vlcg>	C57BL/6N-Gas6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797552	F	MP:0002092	abnormal eye morphology	Gas6<tm1.1(KOMP)Vlcg>/Gas6<tm1.1(KOMP)Vlcg>	C57BL/6N-Gas6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797552	F	MP:0002968	increased circulating alkaline phosphatase level	Gas6<tm1.1(KOMP)Vlcg>/Gas6<tm1.1(KOMP)Vlcg>	C57BL/6N-Gas6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797553	F	MP:0002060	abnormal skin morphology	Castor1<tm1.1(KOMP)Vlcg>/Castor1<tm1.1(KOMP)Vlcg>	C57BL/6N-Castor1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797554	M	MP:0002644	decreased circulating triglyceride level	Gc<tm1.1(KOMP)Vlcg>/Gc<tm1.1(KOMP)Vlcg>	C57BL/6N-Gc<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797554	M	MP:0005567	decreased circulating total protein level	Gc<tm1.1(KOMP)Vlcg>/Gc<tm1.1(KOMP)Vlcg>	C57BL/6N-Gc<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797554	M	MP:0005560	decreased circulating glucose level	Gc<tm1.1(KOMP)Vlcg>/Gc<tm1.1(KOMP)Vlcg>	C57BL/6N-Gc<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797554	M	MP:0000186	decreased circulating HDL cholesterol level	Gc<tm1.1(KOMP)Vlcg>/Gc<tm1.1(KOMP)Vlcg>	C57BL/6N-Gc<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797554	M	MP:0005179	decreased circulating cholesterol level	Gc<tm1.1(KOMP)Vlcg>/Gc<tm1.1(KOMP)Vlcg>	C57BL/6N-Gc<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797554	M	MP:0002941	increased circulating alanine transaminase level	Gc<tm1.1(KOMP)Vlcg>/Gc<tm1.1(KOMP)Vlcg>	C57BL/6N-Gc<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797555	F	MP:0002590	increased mean corpuscular volume	Gdf2<tm1.1(KOMP)Vlcg>/Gdf2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gdf2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797555	F	MP:0000274	enlarged heart	Gdf2<tm1.1(KOMP)Vlcg>/Gdf2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gdf2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797557	F	MP:0002875	decreased erythrocyte cell number	Gimap8<tm1.1(KOMP)Vlcg>/Gimap8<tm1.1(KOMP)Vlcg>	C57BL/6N-Gimap8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797558	F	MP:0002590	increased mean corpuscular volume	Gjb3<tm1.1(KOMP)Vlcg>/Gjb3<+>	C57BL/6N-Gjb3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797559	F	MP:0000691	enlarged spleen	Gjb4<tm1.1(KOMP)Vlcg>/Gjb4<tm1.1(KOMP)Vlcg>	C57BL/6N-Gjb4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797559	M	MP:0000598	abnormal liver morphology	Gjb4<tm1.1(KOMP)Vlcg>/Gjb4<tm1.1(KOMP)Vlcg>	C57BL/6N-Gjb4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797559	F	MP:0009709	hydrometra	Gjb4<tm1.1(KOMP)Vlcg>/Gjb4<tm1.1(KOMP)Vlcg>	C57BL/6N-Gjb4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797559	F	MP:0001120	abnormal uterus morphology	Gjb4<tm1.1(KOMP)Vlcg>/Gjb4<tm1.1(KOMP)Vlcg>	C57BL/6N-Gjb4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797559	F	MP:0004906	enlarged uterus	Gjb4<tm1.1(KOMP)Vlcg>/Gjb4<tm1.1(KOMP)Vlcg>	C57BL/6N-Gjb4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797559	F	MP:0000689	abnormal spleen morphology	Gjb4<tm1.1(KOMP)Vlcg>/Gjb4<tm1.1(KOMP)Vlcg>	C57BL/6N-Gjb4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797561	M	MP:0010025	decreased total body fat amount	Gkn2<tm1.1(KOMP)Vlcg>/Gkn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797561	M	MP:0000274	enlarged heart	Gkn2<tm1.1(KOMP)Vlcg>/Gkn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797561	M	MP:0002175	decreased brain weight	Gkn2<tm1.1(KOMP)Vlcg>/Gkn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797561	F	MP:0013278	decreased fasting circulating glucose level	Gkn2<tm1.1(KOMP)Vlcg>/Gkn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797561	F	MP:0002591	decreased mean corpuscular volume	Gkn2<tm1.1(KOMP)Vlcg>/Gkn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797561	M	MP:0003960	increased lean body mass	Gkn2<tm1.1(KOMP)Vlcg>/Gkn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797561	M	MP:0002544	brachydactyly	Gkn2<tm1.1(KOMP)Vlcg>/Gkn2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gkn2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797562	M	MP:0008806	increased circulating amylase level	Pramel31<tm2b(KOMP)Wtsi>/Pramel31<tm2b(KOMP)Wtsi>	C57BL/6N-Pramel31<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797563	M	MP:0005178	increased circulating cholesterol level	Ct45a<tm1e(KOMP)Wtsi>/Y	C57BL/6N-Ct45a<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797563	M	MP:0000182	increased circulating LDL cholesterol level	Ct45a<tm1e(KOMP)Wtsi>/Y	C57BL/6N-Ct45a<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797563	M	MP:0001556	increased circulating HDL cholesterol level	Ct45a<tm1e(KOMP)Wtsi>/Y	C57BL/6N-Ct45a<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797564	F	MP:0005178	increased circulating cholesterol level	Ct45a<tm1e(KOMP)Wtsi>/Ct45a<tm1e(KOMP)Wtsi>	C57BL/6N-Ct45a<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797564	F	MP:0001556	increased circulating HDL cholesterol level	Ct45a<tm1e(KOMP)Wtsi>/Ct45a<tm1e(KOMP)Wtsi>	C57BL/6N-Ct45a<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797565	M	MP:0005016	decreased lymphocyte cell number	Pou2af3<tm1b(NCOM)Mfgc>/Pou2af3<tm1b(NCOM)Mfgc>	C57BL/6N-Pou2af3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797565	M	MP:0000219	increased neutrophil cell number	Pou2af3<tm1b(NCOM)Mfgc>/Pou2af3<tm1b(NCOM)Mfgc>	C57BL/6N-Pou2af3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797565	F	MP:0002764	short tibia	Pou2af3<tm1b(NCOM)Mfgc>/Pou2af3<tm1b(NCOM)Mfgc>	C57BL/6N-Pou2af3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797565	F	MP:0001566	increased circulating phosphate level	Pou2af3<tm1b(NCOM)Mfgc>/Pou2af3<tm1b(NCOM)Mfgc>	C57BL/6N-Pou2af3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797565	M	MP:0001925	male infertility	Pou2af3<tm1b(NCOM)Mfgc>/Pou2af3<tm1b(NCOM)Mfgc>	C57BL/6N-Pou2af3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797565	M	MP:0010052	increased grip strength	Pou2af3<tm1b(NCOM)Mfgc>/Pou2af3<tm1b(NCOM)Mfgc>	C57BL/6N-Pou2af3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797565	F	MP:0005565	increased blood urea nitrogen level	Pou2af3<tm1b(NCOM)Mfgc>/Pou2af3<tm1b(NCOM)Mfgc>	C57BL/6N-Pou2af3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797565	F	MP:0003928	increased heart rate variability	Pou2af3<tm1b(NCOM)Mfgc>/Pou2af3<tm1b(NCOM)Mfgc>	C57BL/6N-Pou2af3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797566	M	MP:0003179	thrombocytopenia	Gna11<tm1b(EUCOMM)Wtsi>/Gna11<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gna11<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797566	F	MP:0002875	decreased erythrocyte cell number	Gna11<tm1b(EUCOMM)Wtsi>/Gna11<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gna11<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797566	M	MP:0002591	decreased mean corpuscular volume	Gna11<tm1b(EUCOMM)Wtsi>/Gna11<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gna11<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797566	M	MP:0004609	vertebral fusion	Gna11<tm1b(EUCOMM)Wtsi>/Gna11<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gna11<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797569	M	MP:0002098	abnormal vibrissa morphology	Gp6<tm2b(EUCOMM)Hmgu>/Gp6<tm2b(EUCOMM)Hmgu>	C57BL/6N-Gp6<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:5797569	M	MP:0005013	increased lymphocyte cell number	Gp6<tm2b(EUCOMM)Hmgu>/Gp6<tm2b(EUCOMM)Hmgu>	C57BL/6N-Gp6<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:5797569	F	MP:0011960	abnormal eye anterior chamber depth	Gp6<tm2b(EUCOMM)Hmgu>/Gp6<tm2b(EUCOMM)Hmgu>	C57BL/6N-Gp6<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:5797569	M	MP:0004357	long tibia	Gp6<tm2b(EUCOMM)Hmgu>/Gp6<tm2b(EUCOMM)Hmgu>	C57BL/6N-Gp6<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:5797571	M	MP:0001147	small testis	Gpbar1<tm1.1(KOMP)Vlcg>/Gpbar1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpbar1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797571	M	MP:0002135	abnormal kidney morphology	Gpbar1<tm1.1(KOMP)Vlcg>/Gpbar1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpbar1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797571	F	MP:0002941	increased circulating alanine transaminase level	Gpbar1<tm1.1(KOMP)Vlcg>/Gpbar1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpbar1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797571	M	MP:0001146	abnormal testis morphology	Gpbar1<tm1.1(KOMP)Vlcg>/Gpbar1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpbar1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797571	M	MP:0002339	abnormal lymph node morphology	Gpbar1<tm1.1(KOMP)Vlcg>/Gpbar1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpbar1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797572	F	MP:0001402	decreased locomotor activity	Gpr101<tm1b(KOMP)Mbp>/Gpr101<tm1b(KOMP)Mbp>	C57BL/6N-Gpr101<tm1b(KOMP)Mbp>/Ics	N	MGI:5576271
MGI:5797572	F	MP:0011960	abnormal eye anterior chamber depth	Gpr101<tm1b(KOMP)Mbp>/Gpr101<tm1b(KOMP)Mbp>	C57BL/6N-Gpr101<tm1b(KOMP)Mbp>/Ics	N	MGI:5576271
MGI:5797572	F	MP:0020870	decreased thigmotaxis	Gpr101<tm1b(KOMP)Mbp>/Gpr101<tm1b(KOMP)Mbp>	C57BL/6N-Gpr101<tm1b(KOMP)Mbp>/Ics	N	MGI:5576271
MGI:5797573	M	MP:0002608	increased hematocrit	Gpr183<tm1.1(KOMP)Vlcg>/Gpr183<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpr183<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797573	M	MP:0003131	increased erythrocyte cell number	Gpr183<tm1.1(KOMP)Vlcg>/Gpr183<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpr183<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797576	M	MP:0002631	abnormal epididymis morphology	Gprc5b<tm1b(EUCOMM)Wtsi>/Gprc5b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gprc5b<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797576	M	MP:0004931	enlarged epididymis	Gprc5b<tm1b(EUCOMM)Wtsi>/Gprc5b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gprc5b<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797578	F	MP:0001402	decreased locomotor activity	Grin2b<tm1e.1(KOMP)Wtsi>/Grin2b<+>	C57BL/6N-Grin2b<tm1e.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797578	M	MP:0001488	increased startle reflex	Grin2b<tm1e.1(KOMP)Wtsi>/Grin2b<+>	C57BL/6N-Grin2b<tm1e.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797578	M	MP:0002599	increased mean platelet volume	Grin2b<tm1e.1(KOMP)Wtsi>/Grin2b<+>	C57BL/6N-Grin2b<tm1e.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797578	M	MP:0000274	enlarged heart	Grin2b<tm1e.1(KOMP)Wtsi>/Grin2b<+>	C57BL/6N-Grin2b<tm1e.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797579	F	MP:0000689	abnormal spleen morphology	Gstm4<tm2b(EUCOMM)Hmgu>/Gstm4<tm2b(EUCOMM)Hmgu>	C57BL/6N-Gstm4<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5797580	M	MP:0013278	decreased fasting circulating glucose level	H13<tm1b(KOMP)Wtsi>/H13<+>	C57BL/6N-H13<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797581	M	MP:0000266	abnormal heart morphology	Hacl1<tm1b(KOMP)Wtsi>/Hacl1<tm1b(KOMP)Wtsi>	C57BL/6N-Hacl1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797581	M	MP:0000274	enlarged heart	Hacl1<tm1b(KOMP)Wtsi>/Hacl1<tm1b(KOMP)Wtsi>	C57BL/6N-Hacl1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797581	M	MP:0002092	abnormal eye morphology	Hacl1<tm1b(KOMP)Wtsi>/Hacl1<tm1b(KOMP)Wtsi>	C57BL/6N-Hacl1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797582	M	MP:0000266	abnormal heart morphology	Havcr2<tm1b(KOMP)Wtsi>/Havcr2<tm1b(KOMP)Wtsi>	C57BL/6N-Havcr2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797582	F	MP:0002135	abnormal kidney morphology	Havcr2<tm1b(KOMP)Wtsi>/Havcr2<tm1b(KOMP)Wtsi>	C57BL/6N-Havcr2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797582	M	MP:0004952	increased spleen weight	Havcr2<tm1b(KOMP)Wtsi>/Havcr2<tm1b(KOMP)Wtsi>	C57BL/6N-Havcr2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797582	M	MP:0000274	enlarged heart	Havcr2<tm1b(KOMP)Wtsi>/Havcr2<tm1b(KOMP)Wtsi>	C57BL/6N-Havcr2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797583	M	MP:0013278	decreased fasting circulating glucose level	Hc<tm1b(EUCOMM)Wtsi>/Hc<tm1b(EUCOMM)Wtsi>	C57BL/6N-Hc<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5797584	M	MP:0000689	abnormal spleen morphology	Hddc3<tm1.1(KOMP)Vlcg>/Hddc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Hddc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797584	F	MP:0001944	abnormal pancreas morphology	Hddc3<tm1.1(KOMP)Vlcg>/Hddc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Hddc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797584	F	MP:0005343	increased circulating aspartate transaminase level	Hddc3<tm1.1(KOMP)Vlcg>/Hddc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Hddc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797584	M	MP:0000598	abnormal liver morphology	Hddc3<tm1.1(KOMP)Vlcg>/Hddc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Hddc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797584	M	MP:0002135	abnormal kidney morphology	Hddc3<tm1.1(KOMP)Vlcg>/Hddc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Hddc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797584	F	MP:0002941	increased circulating alanine transaminase level	Hddc3<tm1.1(KOMP)Vlcg>/Hddc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Hddc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797584	M	MP:0000691	enlarged spleen	Hddc3<tm1.1(KOMP)Vlcg>/Hddc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Hddc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797584	M	MP:0001925	male infertility	Hddc3<tm1.1(KOMP)Vlcg>/Hddc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Hddc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797584	F	MP:0000274	enlarged heart	Hddc3<tm1.1(KOMP)Vlcg>/Hddc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Hddc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797585	F	MP:0005562	decreased mean corpuscular hemoglobin	Hemgn<tm1.1(KOMP)Vlcg>/Hemgn<tm1.1(KOMP)Vlcg>	C57BL/6N-Hemgn<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797585	F	MP:0002591	decreased mean corpuscular volume	Hemgn<tm1.1(KOMP)Vlcg>/Hemgn<tm1.1(KOMP)Vlcg>	C57BL/6N-Hemgn<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797586	M	MP:0003179	thrombocytopenia	Herc6<tm1b(EUCOMM)Hmgu>/Herc6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Herc6<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5797586	M	MP:0002606	increased basophil cell number	Herc6<tm1b(EUCOMM)Hmgu>/Herc6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Herc6<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5797586	M	MP:0005011	increased eosinophil cell number	Herc6<tm1b(EUCOMM)Hmgu>/Herc6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Herc6<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5797587	M	MP:0004952	increased spleen weight	Hmox2<tm1b(EUCOMM)Hmgu>/Hmox2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hmox2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797587	M	MP:0000274	enlarged heart	Hmox2<tm1b(EUCOMM)Hmgu>/Hmox2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hmox2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797587	M	MP:0010067	increased red blood cell distribution width	Hmox2<tm1b(EUCOMM)Hmgu>/Hmox2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hmox2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797588	M	MP:0003917	increased kidney weight	Hmx2<tm1.1(KOMP)Vlcg>/Hmx2<tm1.1(KOMP)Vlcg>	C57BL/6N-Hmx2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797588	F	MP:0011110	preweaning lethality, incomplete penetrance	Hmx2<tm1.1(KOMP)Vlcg>/Hmx2<tm1.1(KOMP)Vlcg>	C57BL/6N-Hmx2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797589	F	MP:0002599	increased mean platelet volume	Hnrnph1<tm1b(KOMP)Wtsi>/Hnrnph1<+>	C57BL/6N-Hnrnph1<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797589	M	MP:0000222	decreased neutrophil cell number	Hnrnph1<tm1b(KOMP)Wtsi>/Hnrnph1<+>	C57BL/6N-Hnrnph1<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797590	M	MP:0002968	increased circulating alkaline phosphatase level	Hook3<tm1b(NCOM)Mfgc>/Hook3<tm1b(NCOM)Mfgc>	C57BL/6N-Hook3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797590	M	MP:0002606	increased basophil cell number	Hook3<tm1b(NCOM)Mfgc>/Hook3<tm1b(NCOM)Mfgc>	C57BL/6N-Hook3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797590	M	MP:0010124	decreased bone mineral content	Hook3<tm1b(NCOM)Mfgc>/Hook3<tm1b(NCOM)Mfgc>	C57BL/6N-Hook3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797590	F	MP:0001175	abnormal lung morphology	Hook3<tm1b(NCOM)Mfgc>/Hook3<tm1b(NCOM)Mfgc>	C57BL/6N-Hook3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797590	M	MP:0001258	decreased body length	Hook3<tm1b(NCOM)Mfgc>/Hook3<tm1b(NCOM)Mfgc>	C57BL/6N-Hook3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797590	M	MP:0005343	increased circulating aspartate transaminase level	Hook3<tm1b(NCOM)Mfgc>/Hook3<tm1b(NCOM)Mfgc>	C57BL/6N-Hook3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797590	M	MP:0010052	increased grip strength	Hook3<tm1b(NCOM)Mfgc>/Hook3<tm1b(NCOM)Mfgc>	C57BL/6N-Hook3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797590	M	MP:0000063	decreased bone mineral density	Hook3<tm1b(NCOM)Mfgc>/Hook3<tm1b(NCOM)Mfgc>	C57BL/6N-Hook3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797591	F	MP:0013278	decreased fasting circulating glucose level	Hoxc12<tm1.1(KOMP)Vlcg>/Hoxc12<tm1.1(KOMP)Vlcg>	C57BL/6N-Hoxc12<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797591	M	MP:0000745	tremors	Hoxc12<tm1.1(KOMP)Vlcg>/Hoxc12<tm1.1(KOMP)Vlcg>	C57BL/6N-Hoxc12<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797593	M	MP:0002960	decreased urine microalbumin level	Hsd17b11<tm1.1(KOMP)Vlcg>/Hsd17b11<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b11<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797593	M	MP:0011471	decreased urine creatinine level	Hsd17b11<tm1.1(KOMP)Vlcg>/Hsd17b11<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b11<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797593	F	MP:0001399	hyperactivity	Hsd17b11<tm1.1(KOMP)Vlcg>/Hsd17b11<tm1.1(KOMP)Vlcg>	C57BL/6N-Hsd17b11<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797594	F	MP:0002702	decreased circulating free fatty acids level	Hspb3<tm1.1(KOMP)Vlcg>/Hspb3<tm1.1(KOMP)Vlcg>	C57BL/6N-Hspb3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797596	F	MP:0000452	abnormal mouth morphology	Ifnk<tm1.1(KOMP)Vlcg>/Ifnk<tm1.1(KOMP)Vlcg>	C57BL/6N-Ifnk<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797598	M	MP:0001556	increased circulating HDL cholesterol level	Il12a<tm1b(EUCOMM)Hmgu>/Il12a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il12a<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797598	F	MP:0004609	vertebral fusion	Il12a<tm1b(EUCOMM)Hmgu>/Il12a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il12a<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797599	F	MP:0011959	abnormal eye posterior chamber depth	Il12rb1<tm1b(KOMP)Wtsi>/Il12rb1<tm1b(KOMP)Wtsi>	C57BL/6N-Il12rb1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5797599	M	MP:0002874	decreased hemoglobin content	Il12rb1<tm1b(KOMP)Wtsi>/Il12rb1<tm1b(KOMP)Wtsi>	C57BL/6N-Il12rb1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5797599	M	MP:0010025	decreased total body fat amount	Il12rb1<tm1b(KOMP)Wtsi>/Il12rb1<tm1b(KOMP)Wtsi>	C57BL/6N-Il12rb1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5797600	M	MP:0001417	decreased exploration in new environment	Il18rap<tm1b(KOMP)Wtsi>/Il18rap<tm1b(KOMP)Wtsi>	C57BL/6N-Il18rap<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:5797600	M	MP:0001925	male infertility	Il18rap<tm1b(KOMP)Wtsi>/Il18rap<tm1b(KOMP)Wtsi>	C57BL/6N-Il18rap<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:5797600	F	MP:0011960	abnormal eye anterior chamber depth	Il18rap<tm1b(KOMP)Wtsi>/Il18rap<tm1b(KOMP)Wtsi>	C57BL/6N-Il18rap<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:5797601	F	MP:0002941	increased circulating alanine transaminase level	Il20ra<tm1.1(KOMP)Vlcg>/Il20ra<tm1.1(KOMP)Vlcg>	C57BL/6N-Il20ra<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797601	F	MP:0005343	increased circulating aspartate transaminase level	Il20ra<tm1.1(KOMP)Vlcg>/Il20ra<tm1.1(KOMP)Vlcg>	C57BL/6N-Il20ra<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797601	M	MP:0010067	increased red blood cell distribution width	Il20ra<tm1.1(KOMP)Vlcg>/Il20ra<tm1.1(KOMP)Vlcg>	C57BL/6N-Il20ra<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797602	M	MP:0004931	enlarged epididymis	Il20rb<tm1b(KOMP)Wtsi>/Il20rb<+>	C57BL/6N-Il20rb<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797603	M	MP:0001891	hydrocephaly	Il20rb<tm1b(KOMP)Wtsi>/Il20rb<tm1b(KOMP)Wtsi>	C57BL/6N-Il20rb<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797603	F	MP:0002941	increased circulating alanine transaminase level	Il20rb<tm1b(KOMP)Wtsi>/Il20rb<tm1b(KOMP)Wtsi>	C57BL/6N-Il20rb<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797603	M	MP:0002152	abnormal brain morphology	Il20rb<tm1b(KOMP)Wtsi>/Il20rb<tm1b(KOMP)Wtsi>	C57BL/6N-Il20rb<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797604	M	MP:0005633	increased circulating sodium level	Il24<tm1.1(KOMP)Vlcg>/Il24<tm1.1(KOMP)Vlcg>	C57BL/6N-Il24<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797605	M	MP:0003961	decreased lean body mass	Il31ra<tm1b(EUCOMM)Hmgu>/Il31ra<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il31ra<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797605	M	MP:0010124	decreased bone mineral content	Il31ra<tm1b(EUCOMM)Hmgu>/Il31ra<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il31ra<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797605	M	MP:0010024	increased total body fat amount	Il31ra<tm1b(EUCOMM)Hmgu>/Il31ra<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il31ra<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797606	F	MP:0001523	impaired righting response	Ipp<tm1.1(KOMP)Vlcg>/Ipp<tm1.1(KOMP)Vlcg>	C57BL/6N-Ipp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797606	M	MP:0003020	decreased circulating chloride level	Ipp<tm1.1(KOMP)Vlcg>/Ipp<tm1.1(KOMP)Vlcg>	C57BL/6N-Ipp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797606	M	MP:0005560	decreased circulating glucose level	Ipp<tm1.1(KOMP)Vlcg>/Ipp<tm1.1(KOMP)Vlcg>	C57BL/6N-Ipp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797606	F	MP:0002968	increased circulating alkaline phosphatase level	Ipp<tm1.1(KOMP)Vlcg>/Ipp<tm1.1(KOMP)Vlcg>	C57BL/6N-Ipp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797606	F	MP:0011396	abnormal sleep behavior	Ipp<tm1.1(KOMP)Vlcg>/Ipp<tm1.1(KOMP)Vlcg>	C57BL/6N-Ipp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797606	F	MP:0000221	decreased leukocyte cell number	Ipp<tm1.1(KOMP)Vlcg>/Ipp<tm1.1(KOMP)Vlcg>	C57BL/6N-Ipp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797607	F	MP:0001402	decreased locomotor activity	Isca1<tm1b(KOMP)Wtsi>/Isca1<+>	C57BL/6N-Isca1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797608	F	MP:0002833	increased heart weight	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0005568	increased circulating total protein level	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	M	MP:0013278	decreased fasting circulating glucose level	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0000194	increased circulating calcium level	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0010088	decreased circulating fructosamine level	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0005343	increased circulating aspartate transaminase level	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	M	MP:0002100	abnormal tooth morphology	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0005565	increased blood urea nitrogen level	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	M	MP:0001486	abnormal startle reflex	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0001566	increased circulating phosphate level	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	M	MP:0011496	abnormal head size	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0003795	abnormal bone structure	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0003068	enlarged kidney	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0000745	tremors	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0000691	enlarged spleen	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0003960	increased lean body mass	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0009342	enlarged gallbladder	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0000467	abnormal esophagus morphology	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0010025	decreased total body fat amount	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797608	F	MP:0000063	decreased bone mineral density	Itch<tm1b(EUCOMM)Hmgu>/Itch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Itch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797609	M	MP:0004930	small epididymis	Itpr1<tm1.1(NCOM)Mfgc>/Itpr1<+>	C57BL/6N-Itpr1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797611	M	MP:0001925	male infertility	Ivl<tm1b(KOMP)Wtsi>/Ivl<tm1b(KOMP)Wtsi>	C57BL/6N-Ivl<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797611	M	MP:0000266	abnormal heart morphology	Ivl<tm1b(KOMP)Wtsi>/Ivl<tm1b(KOMP)Wtsi>	C57BL/6N-Ivl<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797611	M	MP:0010025	decreased total body fat amount	Ivl<tm1b(KOMP)Wtsi>/Ivl<tm1b(KOMP)Wtsi>	C57BL/6N-Ivl<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797611	M	MP:0001891	hydrocephaly	Ivl<tm1b(KOMP)Wtsi>/Ivl<tm1b(KOMP)Wtsi>	C57BL/6N-Ivl<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797611	M	MP:0002152	abnormal brain morphology	Ivl<tm1b(KOMP)Wtsi>/Ivl<tm1b(KOMP)Wtsi>	C57BL/6N-Ivl<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797611	M	MP:0000274	enlarged heart	Ivl<tm1b(KOMP)Wtsi>/Ivl<tm1b(KOMP)Wtsi>	C57BL/6N-Ivl<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797612	F	MP:0008935	decreased mean platelet volume	Jmjd6<tm1b(EUCOMM)Wtsi>/Jmjd6<+>	C57BL/6N-Jmjd6<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5797613	M	MP:0004151	decreased circulating iron level	Jmjd8<tm1.1(KOMP)Vlcg>/Jmjd8<tm1.1(KOMP)Vlcg>	C57BL/6N-Jmjd8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797615	F	MP:0002874	decreased hemoglobin content	Kcnj11<tm1b(EUCOMM)Wtsi>/Kcnj11<tm1b(EUCOMM)Wtsi>	C57BL/6N-Kcnj11<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797615	F	MP:0013278	decreased fasting circulating glucose level	Kcnj11<tm1b(EUCOMM)Wtsi>/Kcnj11<tm1b(EUCOMM)Wtsi>	C57BL/6N-Kcnj11<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797616	M	MP:0004931	enlarged epididymis	Kcnk18<tm1.1(KOMP)Vlcg>/Kcnk18<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnk18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797616	M	MP:0002631	abnormal epididymis morphology	Kcnk18<tm1.1(KOMP)Vlcg>/Kcnk18<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnk18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797617	F	MP:0002968	increased circulating alkaline phosphatase level	Kif3c<tm1.1(KOMP)Vlcg>/Kif3c<+>	C57BL/6N-Kif3c<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797617	F	MP:0001399	hyperactivity	Kif3c<tm1.1(KOMP)Vlcg>/Kif3c<+>	C57BL/6N-Kif3c<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797619	F	MP:0000266	abnormal heart morphology	Klf9<tm1.1(KOMP)Vlcg>/Klf9<tm1.1(KOMP)Vlcg>	C57BL/6N-Klf9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797619	F	MP:0000274	enlarged heart	Klf9<tm1.1(KOMP)Vlcg>/Klf9<tm1.1(KOMP)Vlcg>	C57BL/6N-Klf9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797621	M	MP:0005627	increased circulating potassium level	Klhl3<tm1b(KOMP)Wtsi>/Klhl3<tm1b(KOMP)Wtsi>	C57BL/6N-Klhl3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797621	M	MP:0002968	increased circulating alkaline phosphatase level	Klhl3<tm1b(KOMP)Wtsi>/Klhl3<tm1b(KOMP)Wtsi>	C57BL/6N-Klhl3<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797622	F	MP:0002959	increased urine microalbumin level	Klk14<tm1.1(KOMP)Vlcg>/Klk14<tm1.1(KOMP)Vlcg>	C57BL/6N-Klk14<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797623	F	MP:0008810	increased circulating iron level	Krt9<tm1.1(KOMP)Vlcg>/Krt9<tm1.1(KOMP)Vlcg>	C57BL/6N-Krt9<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797624	M	MP:0002941	increased circulating alanine transaminase level	Lama1<tm2b(EUCOMM)Hmgu>/Lama1<+>	C57BL/6N-Lama1<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797625	F	MP:0001488	increased startle reflex	Laptm4b<tm1e.1(KOMP)Wtsi>/Laptm4b<+>	C57BL/6N-Laptm4b<tm1e.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797625	F	MP:0009142	decreased prepulse inhibition	Laptm4b<tm1e.1(KOMP)Wtsi>/Laptm4b<+>	C57BL/6N-Laptm4b<tm1e.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797626	F	MP:0011100	preweaning lethality, complete penetrance	Laptm4b<tm1e.1(KOMP)Wtsi>/Laptm4b<tm1e.1(KOMP)Wtsi>	C57BL/6N-Laptm4b<tm1e.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797627	M	MP:0002941	increased circulating alanine transaminase level	Ldlrad4<tm1b(EUCOMM)Wtsi>/Ldlrad4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ldlrad4<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797628	M	MP:0000221	decreased leukocyte cell number	Lepr<tm1b(EUCOMM)Wtsi>/Lepr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lepr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797628	F	MP:0005627	increased circulating potassium level	Lepr<tm1b(EUCOMM)Wtsi>/Lepr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lepr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797628	F	MP:0001926	female infertility	Lepr<tm1b(EUCOMM)Wtsi>/Lepr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lepr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797628	M	MP:0005561	increased mean corpuscular hemoglobin	Lepr<tm1b(EUCOMM)Wtsi>/Lepr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lepr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797628	M	MP:0003179	thrombocytopenia	Lepr<tm1b(EUCOMM)Wtsi>/Lepr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lepr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797628	M	MP:0002599	increased mean platelet volume	Lepr<tm1b(EUCOMM)Wtsi>/Lepr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lepr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797628	F	MP:0003795	abnormal bone structure	Lepr<tm1b(EUCOMM)Wtsi>/Lepr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lepr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797628	M	MP:0001925	male infertility	Lepr<tm1b(EUCOMM)Wtsi>/Lepr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lepr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797628	M	MP:0008806	increased circulating amylase level	Lepr<tm1b(EUCOMM)Wtsi>/Lepr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lepr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797628	F	MP:0000220	increased monocyte cell number	Lepr<tm1b(EUCOMM)Wtsi>/Lepr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lepr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797628	M	MP:0001157	small seminal vesicle	Lepr<tm1b(EUCOMM)Wtsi>/Lepr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lepr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797628	F	MP:0008810	increased circulating iron level	Lepr<tm1b(EUCOMM)Wtsi>/Lepr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lepr<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797629	F	MP:0002764	short tibia	Lgmn<tm1b(NCOM)Mfgc>/Lgmn<tm1b(NCOM)Mfgc>	C57BL/6N-Lgmn<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797629	F	MP:0009142	decreased prepulse inhibition	Lgmn<tm1b(NCOM)Mfgc>/Lgmn<tm1b(NCOM)Mfgc>	C57BL/6N-Lgmn<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797629	F	MP:0001258	decreased body length	Lgmn<tm1b(NCOM)Mfgc>/Lgmn<tm1b(NCOM)Mfgc>	C57BL/6N-Lgmn<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797630	M	MP:0002059	abnormal seminal vesicle morphology	Lhfpl1<tm1.1(NCOM)Mfgc>/Y	C57BL/6N-Lhfpl1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797633	M	MP:0001417	decreased exploration in new environment	Lin28b<tm1b(EUCOMM)Hmgu>/Lin28b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lin28b<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797634	F	MP:0005560	decreased circulating glucose level	Lipn<tm1.1(KOMP)Vlcg>/Lipn<tm1.1(KOMP)Vlcg>	C57BL/6N-Lipn<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797635	F	MP:0001303	abnormal lens morphology	Lonp1<tm1b(EUCOMM)Hmgu>/Lonp1<+>	C57BL/6N-Lonp1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797635	F	MP:0001556	increased circulating HDL cholesterol level	Lonp1<tm1b(EUCOMM)Hmgu>/Lonp1<+>	C57BL/6N-Lonp1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797636	F	MP:0001303	abnormal lens morphology	Lpo<tm1b(EUCOMM)Wtsi>/Lpo<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lpo<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:5797637	M	MP:0001925	male infertility	Lrrc23<tm1a(EUCOMM)Wtsi>/Lrrc23<tm1a(EUCOMM)Wtsi>	C57BL/6N-Lrrc23<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797638	M	MP:0001925	male infertility	Lrrc71<tm1a(KOMP)Wtsi>/Lrrc71<tm1a(KOMP)Wtsi>	C57BL/6N-Lrrc71<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797639	M	MP:0001891	hydrocephaly	Lrrcc1<tm1b(EUCOMM)Wtsi>/Lrrcc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lrrcc1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797639	M	MP:0002152	abnormal brain morphology	Lrrcc1<tm1b(EUCOMM)Wtsi>/Lrrcc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lrrcc1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797639	M	MP:0001925	male infertility	Lrrcc1<tm1b(EUCOMM)Wtsi>/Lrrcc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lrrcc1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797639	F	MP:0002875	decreased erythrocyte cell number	Lrrcc1<tm1b(EUCOMM)Wtsi>/Lrrcc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Lrrcc1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797640	F	MP:0013279	increased fasting circulating glucose level	Ltbp2<tm2b(KOMP)Wtsi>/Ltbp2<tm2b(KOMP)Wtsi>	C57BL/6N-Ltbp2<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797642	F	MP:0009709	hydrometra	Lypd6<tm1b(KOMP)Wtsi>/Lypd6<+>	C57BL/6N-Lypd6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797642	F	MP:0002060	abnormal skin morphology	Lypd6<tm1b(KOMP)Wtsi>/Lypd6<+>	C57BL/6N-Lypd6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797642	M	MP:0001146	abnormal testis morphology	Lypd6<tm1b(KOMP)Wtsi>/Lypd6<+>	C57BL/6N-Lypd6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797642	M	MP:0001147	small testis	Lypd6<tm1b(KOMP)Wtsi>/Lypd6<+>	C57BL/6N-Lypd6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797642	F	MP:0001192	scaly skin	Lypd6<tm1b(KOMP)Wtsi>/Lypd6<+>	C57BL/6N-Lypd6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797642	F	MP:0001102	small superior vagus ganglion	Lypd6<tm1b(KOMP)Wtsi>/Lypd6<+>	C57BL/6N-Lypd6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797642	F	MP:0001200	thick skin	Lypd6<tm1b(KOMP)Wtsi>/Lypd6<+>	C57BL/6N-Lypd6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797643	M	MP:0005013	increased lymphocyte cell number	Mamld1<tm1.1(NCOM)Mfgc>/Y	C57BL/6N-Mamld1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797643	M	MP:0005278	abnormal cholesterol homeostasis	Mamld1<tm1.1(NCOM)Mfgc>/Y	C57BL/6N-Mamld1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797643	M	MP:0009142	decreased prepulse inhibition	Mamld1<tm1.1(NCOM)Mfgc>/Y	C57BL/6N-Mamld1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797643	M	MP:0002764	short tibia	Mamld1<tm1.1(NCOM)Mfgc>/Y	C57BL/6N-Mamld1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797643	M	MP:0010379	decreased respiratory quotient	Mamld1<tm1.1(NCOM)Mfgc>/Y	C57BL/6N-Mamld1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797643	M	MP:0000218	increased leukocyte cell number	Mamld1<tm1.1(NCOM)Mfgc>/Y	C57BL/6N-Mamld1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797644	F	MP:0001258	decreased body length	Mamld1<tm1.1(NCOM)Mfgc>/Mamld1<tm1.1(NCOM)Mfgc>	C57BL/6N-Mamld1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797644	F	MP:0009142	decreased prepulse inhibition	Mamld1<tm1.1(NCOM)Mfgc>/Mamld1<tm1.1(NCOM)Mfgc>	C57BL/6N-Mamld1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797644	F	MP:0010024	increased total body fat amount	Mamld1<tm1.1(NCOM)Mfgc>/Mamld1<tm1.1(NCOM)Mfgc>	C57BL/6N-Mamld1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797644	F	MP:0003795	abnormal bone structure	Mamld1<tm1.1(NCOM)Mfgc>/Mamld1<tm1.1(NCOM)Mfgc>	C57BL/6N-Mamld1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797644	F	MP:0003961	decreased lean body mass	Mamld1<tm1.1(NCOM)Mfgc>/Mamld1<tm1.1(NCOM)Mfgc>	C57BL/6N-Mamld1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797644	F	MP:0010124	decreased bone mineral content	Mamld1<tm1.1(NCOM)Mfgc>/Mamld1<tm1.1(NCOM)Mfgc>	C57BL/6N-Mamld1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797644	F	MP:0002764	short tibia	Mamld1<tm1.1(NCOM)Mfgc>/Mamld1<tm1.1(NCOM)Mfgc>	C57BL/6N-Mamld1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797646	F	MP:0010123	increased bone mineral content	Mas1<tm1.1(KOMP)Vlcg>/Mas1<tm1.1(KOMP)Vlcg>	C57BL/6N-Mas1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797646	M	MP:0002764	short tibia	Mas1<tm1.1(KOMP)Vlcg>/Mas1<tm1.1(KOMP)Vlcg>	C57BL/6N-Mas1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797646	F	MP:0003795	abnormal bone structure	Mas1<tm1.1(KOMP)Vlcg>/Mas1<tm1.1(KOMP)Vlcg>	C57BL/6N-Mas1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797647	M	MP:0006358	absent pinna reflex	Mau2<tm1b(KOMP)Wtsi>/Mau2<+>	C57BL/6N-Mau2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797647	F	MP:0001304	cataract	Mau2<tm1b(KOMP)Wtsi>/Mau2<+>	C57BL/6N-Mau2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797647	F	MP:0003036	vertebral transformation	Mau2<tm1b(KOMP)Wtsi>/Mau2<+>	C57BL/6N-Mau2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797647	F	MP:0001303	abnormal lens morphology	Mau2<tm1b(KOMP)Wtsi>/Mau2<+>	C57BL/6N-Mau2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797648	M	MP:0001157	small seminal vesicle	Mboat7<tm1b(KOMP)Wtsi>/Mboat7<+>	C57BL/6N-Mboat7<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797648	M	MP:0003961	decreased lean body mass	Mboat7<tm1b(KOMP)Wtsi>/Mboat7<+>	C57BL/6N-Mboat7<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797648	F	MP:0005013	increased lymphocyte cell number	Mboat7<tm1b(KOMP)Wtsi>/Mboat7<+>	C57BL/6N-Mboat7<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797650	M	MP:0010052	increased grip strength	Mcm4<tm1b(KOMP)Mbp>/Mcm4<+>	C57BL/6N-Mcm4<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5797651	F	MP:0001510	abnormal coat appearance	Mdp1<tm1.1(KOMP)Vlcg>/Mdp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Mdp1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797653	M	MP:0002631	abnormal epididymis morphology	Mfsd2a<tm1b(KOMP)Wtsi>/Mfsd2a<+>	C57BL/6N-Mfsd2a<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797653	M	MP:0001146	abnormal testis morphology	Mfsd2a<tm1b(KOMP)Wtsi>/Mfsd2a<+>	C57BL/6N-Mfsd2a<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797653	M	MP:0004931	enlarged epididymis	Mfsd2a<tm1b(KOMP)Wtsi>/Mfsd2a<+>	C57BL/6N-Mfsd2a<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797653	M	MP:0001148	enlarged testis	Mfsd2a<tm1b(KOMP)Wtsi>/Mfsd2a<+>	C57BL/6N-Mfsd2a<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797655	F	MP:0002574	increased vertical activity	Mid1ip1<tm1.1(KOMP)Vlcg>/Mid1ip1<tm1.1(KOMP)Vlcg>	C57BL/6N-Mid1ip1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797656	F	MP:0005343	increased circulating aspartate transaminase level	Mkrn2<tm1b(KOMP)Wtsi>/Mkrn2<tm1b(KOMP)Wtsi>	C57BL/6N-Mkrn2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797656	M	MP:0001925	male infertility	Mkrn2<tm1b(KOMP)Wtsi>/Mkrn2<tm1b(KOMP)Wtsi>	C57BL/6N-Mkrn2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797657	M	MP:0000702	enlarged lymph nodes	Mmachc<tm1.1(NCOM)Mfgc>/Mmachc<+>	C57BL/6N-Mmachc<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797657	M	MP:0002989	small kidney	Mmachc<tm1.1(NCOM)Mfgc>/Mmachc<+>	C57BL/6N-Mmachc<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797657	M	MP:0002631	abnormal epididymis morphology	Mmachc<tm1.1(NCOM)Mfgc>/Mmachc<+>	C57BL/6N-Mmachc<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797658	F	MP:0011100	preweaning lethality, complete penetrance	Mmachc<tm1.1(NCOM)Mfgc>/Mmachc<tm1.1(NCOM)Mfgc>	C57BL/6N-Mmachc<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797659	M	MP:0011239	abnormal skin coloration	Mogs<tm1.1(KOMP)Vlcg>/Mogs<+>	C57BL/6N-Mogs<tm1.1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5797660	M	MP:0002544	brachydactyly	Mogs<tm1(KOMP)Vlcg>/Mogs<+>	C57BL/6N-Mogs<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5797660	F	MP:0005313	absent adrenal gland	Mogs<tm1(KOMP)Vlcg>/Mogs<+>	C57BL/6N-Mogs<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5797660	M	MP:0000467	abnormal esophagus morphology	Mogs<tm1(KOMP)Vlcg>/Mogs<+>	C57BL/6N-Mogs<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5797660	M	MP:0000709	enlarged thymus	Mogs<tm1(KOMP)Vlcg>/Mogs<+>	C57BL/6N-Mogs<tm1(KOMP)Vlcg>/Bay	N	MGI:5576271
MGI:5797661	F	MP:0011965	decreased total retina thickness	Mtmr12<tm1b(KOMP)Wtsi>/Mtmr12<tm1b(KOMP)Wtsi>	C57BL/6N-Mtmr12<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797661	M	MP:0001417	decreased exploration in new environment	Mtmr12<tm1b(KOMP)Wtsi>/Mtmr12<tm1b(KOMP)Wtsi>	C57BL/6N-Mtmr12<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797661	F	MP:0010053	decreased grip strength	Mtmr12<tm1b(KOMP)Wtsi>/Mtmr12<tm1b(KOMP)Wtsi>	C57BL/6N-Mtmr12<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:5797663	M	MP:0000266	abnormal heart morphology	Myb<tm1b(KOMP)Wtsi>/Myb<+>	C57BL/6N-Myb<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797663	M	MP:0000274	enlarged heart	Myb<tm1b(KOMP)Wtsi>/Myb<+>	C57BL/6N-Myb<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797664	M	MP:0001516	abnormal motor coordination/balance	Myo1h<tm1b(KOMP)Wtsi>/Myo1h<+>	C57BL/6N-Myo1h<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797665	F	MP:0005293	impaired glucose tolerance	Myo3a<tm1b(KOMP)Wtsi>/Myo3a<tm1b(KOMP)Wtsi>	C57BL/6N-Myo3a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797666	M	MP:0002833	increased heart weight	Myo3b<tm1b(EUCOMM)Hmgu>/Myo3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Myo3b<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797666	F	MP:0000947	convulsive seizures	Myo3b<tm1b(EUCOMM)Hmgu>/Myo3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Myo3b<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797666	F	MP:0003795	abnormal bone structure	Myo3b<tm1b(EUCOMM)Hmgu>/Myo3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Myo3b<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797666	M	MP:0000221	decreased leukocyte cell number	Myo3b<tm1b(EUCOMM)Hmgu>/Myo3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Myo3b<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797667	M	MP:0002075	abnormal coat/hair pigmentation	Nadk2<tm1b(EUCOMM)Wtsi>/Nadk2<+>	C57BL/6N-Nadk2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797668	F	MP:0005542	cornea vascularization	Nadsyn1<tm1b(KOMP)Wtsi>/Nadsyn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nadsyn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797668	M	MP:0005333	decreased heart rate	Nadsyn1<tm1b(KOMP)Wtsi>/Nadsyn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nadsyn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797668	F	MP:0001926	female infertility	Nadsyn1<tm1b(KOMP)Wtsi>/Nadsyn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nadsyn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797668	M	MP:0000691	enlarged spleen	Nadsyn1<tm1b(KOMP)Wtsi>/Nadsyn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nadsyn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797668	F	MP:0010053	decreased grip strength	Nadsyn1<tm1b(KOMP)Wtsi>/Nadsyn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nadsyn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797668	F	MP:0010570	prolonged ST segment	Nadsyn1<tm1b(KOMP)Wtsi>/Nadsyn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nadsyn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797669	M	MP:0010024	increased total body fat amount	Ncbp3<tm1b(EUCOMM)Wtsi>/Ncbp3<+>	C57BL/6N-Ncbp3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797669	M	MP:0000274	enlarged heart	Ncbp3<tm1b(EUCOMM)Wtsi>/Ncbp3<+>	C57BL/6N-Ncbp3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797670	M	MP:0002968	increased circulating alkaline phosphatase level	Ncoa1<tm1.1(KOMP)Vlcg>/Ncoa1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncoa1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797670	M	MP:0010025	decreased total body fat amount	Ncoa1<tm1.1(KOMP)Vlcg>/Ncoa1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncoa1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797670	M	MP:0003960	increased lean body mass	Ncoa1<tm1.1(KOMP)Vlcg>/Ncoa1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncoa1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797670	M	MP:0001399	hyperactivity	Ncoa1<tm1.1(KOMP)Vlcg>/Ncoa1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncoa1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797670	M	MP:0001891	hydrocephaly	Ncoa1<tm1.1(KOMP)Vlcg>/Ncoa1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncoa1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797670	F	MP:0013278	decreased fasting circulating glucose level	Ncoa1<tm1.1(KOMP)Vlcg>/Ncoa1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncoa1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797670	M	MP:0002152	abnormal brain morphology	Ncoa1<tm1.1(KOMP)Vlcg>/Ncoa1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncoa1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797671	M	MP:0005344	increased circulating bilirubin level	Ncoa3<tm1b(EUCOMM)Wtsi>/Ncoa3<+>	C57BL/6N-Ncoa3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797671	M	MP:0002100	abnormal tooth morphology	Ncoa3<tm1b(EUCOMM)Wtsi>/Ncoa3<+>	C57BL/6N-Ncoa3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797671	M	MP:0001289	persistence of hyaloid vascular system	Ncoa3<tm1b(EUCOMM)Wtsi>/Ncoa3<+>	C57BL/6N-Ncoa3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797671	M	MP:0005293	impaired glucose tolerance	Ncoa3<tm1b(EUCOMM)Wtsi>/Ncoa3<+>	C57BL/6N-Ncoa3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797672	F	MP:0010124	decreased bone mineral content	Negr1<tm1b(KOMP)Wtsi>/Negr1<tm1b(KOMP)Wtsi>	C57BL/6N-Negr1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797672	M	MP:0000274	enlarged heart	Negr1<tm1b(KOMP)Wtsi>/Negr1<tm1b(KOMP)Wtsi>	C57BL/6N-Negr1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797672	F	MP:0000063	decreased bone mineral density	Negr1<tm1b(KOMP)Wtsi>/Negr1<tm1b(KOMP)Wtsi>	C57BL/6N-Negr1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797672	M	MP:0000266	abnormal heart morphology	Negr1<tm1b(KOMP)Wtsi>/Negr1<tm1b(KOMP)Wtsi>	C57BL/6N-Negr1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797672	M	MP:0002092	abnormal eye morphology	Negr1<tm1b(KOMP)Wtsi>/Negr1<tm1b(KOMP)Wtsi>	C57BL/6N-Negr1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797672	M	MP:0002175	decreased brain weight	Negr1<tm1b(KOMP)Wtsi>/Negr1<tm1b(KOMP)Wtsi>	C57BL/6N-Negr1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797673	M	MP:0001523	impaired righting response	Nek11<tm1b(KOMP)Wtsi>/Nek11<tm1b(KOMP)Wtsi>	C57BL/6N-Nek11<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797673	F	MP:0004151	decreased circulating iron level	Nek11<tm1b(KOMP)Wtsi>/Nek11<tm1b(KOMP)Wtsi>	C57BL/6N-Nek11<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797673	F	MP:0005560	decreased circulating glucose level	Nek11<tm1b(KOMP)Wtsi>/Nek11<tm1b(KOMP)Wtsi>	C57BL/6N-Nek11<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797674	M	MP:0005179	decreased circulating cholesterol level	Nemf<tm1b(EUCOMM)Hmgu>/Nemf<+>	B6N(Cg)-Nemf<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797675	M	MP:0000703	abnormal thymus morphology	Nfil3<tm1.1(KOMP)Vlcg>/Nfil3<tm1.1(KOMP)Vlcg>	C57BL/6N-Nfil3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797675	M	MP:0000689	abnormal spleen morphology	Nfil3<tm1.1(KOMP)Vlcg>/Nfil3<tm1.1(KOMP)Vlcg>	C57BL/6N-Nfil3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797675	F	MP:0010124	decreased bone mineral content	Nfil3<tm1.1(KOMP)Vlcg>/Nfil3<tm1.1(KOMP)Vlcg>	C57BL/6N-Nfil3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797675	M	MP:0004952	increased spleen weight	Nfil3<tm1.1(KOMP)Vlcg>/Nfil3<tm1.1(KOMP)Vlcg>	C57BL/6N-Nfil3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797675	M	MP:0011110	preweaning lethality, incomplete penetrance	Nfil3<tm1.1(KOMP)Vlcg>/Nfil3<tm1.1(KOMP)Vlcg>	C57BL/6N-Nfil3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797675	M	MP:0000494	abnormal cecum morphology	Nfil3<tm1.1(KOMP)Vlcg>/Nfil3<tm1.1(KOMP)Vlcg>	C57BL/6N-Nfil3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797675	M	MP:0001312	abnormal cornea morphology	Nfil3<tm1.1(KOMP)Vlcg>/Nfil3<tm1.1(KOMP)Vlcg>	C57BL/6N-Nfil3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797675	M	MP:0001944	abnormal pancreas morphology	Nfil3<tm1.1(KOMP)Vlcg>/Nfil3<tm1.1(KOMP)Vlcg>	C57BL/6N-Nfil3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797675	M	MP:0000691	enlarged spleen	Nfil3<tm1.1(KOMP)Vlcg>/Nfil3<tm1.1(KOMP)Vlcg>	C57BL/6N-Nfil3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797675	M	MP:0005542	cornea vascularization	Nfil3<tm1.1(KOMP)Vlcg>/Nfil3<tm1.1(KOMP)Vlcg>	C57BL/6N-Nfil3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797675	M	MP:0000706	small thymus	Nfil3<tm1.1(KOMP)Vlcg>/Nfil3<tm1.1(KOMP)Vlcg>	C57BL/6N-Nfil3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797676	M	MP:0001147	small testis	Nhsl1<tm1.1(KOMP)Vlcg>/Nhsl1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nhsl1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797676	M	MP:0001146	abnormal testis morphology	Nhsl1<tm1.1(KOMP)Vlcg>/Nhsl1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nhsl1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797676	M	MP:0001175	abnormal lung morphology	Nhsl1<tm1.1(KOMP)Vlcg>/Nhsl1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nhsl1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797677	M	MP:0000438	abnormal cranium morphology	Nisch<tm1b(EUCOMM)Hmgu>/Nisch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nisch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797677	F	MP:0003795	abnormal bone structure	Nisch<tm1b(EUCOMM)Hmgu>/Nisch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nisch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797677	F	MP:0001566	increased circulating phosphate level	Nisch<tm1b(EUCOMM)Hmgu>/Nisch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nisch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797677	F	MP:0001402	decreased locomotor activity	Nisch<tm1b(EUCOMM)Hmgu>/Nisch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nisch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797677	F	MP:0010124	decreased bone mineral content	Nisch<tm1b(EUCOMM)Hmgu>/Nisch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nisch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797677	F	MP:0005178	increased circulating cholesterol level	Nisch<tm1b(EUCOMM)Hmgu>/Nisch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nisch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797677	M	MP:0000455	abnormal maxilla morphology	Nisch<tm1b(EUCOMM)Hmgu>/Nisch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nisch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797677	F	MP:0001552	increased circulating triglyceride level	Nisch<tm1b(EUCOMM)Hmgu>/Nisch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nisch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797677	M	MP:0001410	head bobbing	Nisch<tm1b(EUCOMM)Hmgu>/Nisch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nisch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797677	F	MP:0001556	increased circulating HDL cholesterol level	Nisch<tm1b(EUCOMM)Hmgu>/Nisch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nisch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797677	M	MP:0004174	abnormal spine curvature	Nisch<tm1b(EUCOMM)Hmgu>/Nisch<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nisch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797679	F	MP:0001314	cornea opacity	Nmral1<tm1.1(KOMP)Vlcg>/Nmral1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nmral1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797679	F	MP:0001399	hyperactivity	Nmral1<tm1.1(KOMP)Vlcg>/Nmral1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nmral1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797679	M	MP:0010378	increased respiratory quotient	Nmral1<tm1.1(KOMP)Vlcg>/Nmral1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nmral1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797681	M	MP:0005566	decreased blood urea nitrogen level	Nmur1<tm1.1(KOMP)Vlcg>/Nmur1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nmur1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797683	F	MP:0005627	increased circulating potassium level	Npc2<tm1e.1(EUCOMM)Wtsi>/Npc2<+>	C57BL/6N-Npc2<tm1e.1(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797683	M	MP:0002768	small adrenal glands	Npc2<tm1e.1(EUCOMM)Wtsi>/Npc2<+>	C57BL/6N-Npc2<tm1e.1(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797684	M	MP:0002135	abnormal kidney morphology	Nr1h3<tm1.1(KOMP)Vlcg>/Nr1h3<tm1.1(KOMP)Vlcg>	C57BL/6N-Nr1h3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797684	F	MP:0002941	increased circulating alanine transaminase level	Nr1h3<tm1.1(KOMP)Vlcg>/Nr1h3<tm1.1(KOMP)Vlcg>	C57BL/6N-Nr1h3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797685	M	MP:0002968	increased circulating alkaline phosphatase level	Nrn1l<tm1.1(KOMP)Vlcg>/Nrn1l<tm1.1(KOMP)Vlcg>	C57BL/6N-Nrn1l<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797686	M	MP:0009142	decreased prepulse inhibition	Nrsn1<tm1.1(KOMP)Vlcg>/Nrsn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nrsn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797686	F	MP:0013279	increased fasting circulating glucose level	Nrsn1<tm1.1(KOMP)Vlcg>/Nrsn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nrsn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797687	M	MP:0008806	increased circulating amylase level	Nrxn1<tm1b(KOMP)Wtsi>/Nrxn1<+>	C57BL/6N-Nrxn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797687	M	MP:0003960	increased lean body mass	Nrxn1<tm1b(KOMP)Wtsi>/Nrxn1<+>	C57BL/6N-Nrxn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797689	F	MP:0002599	increased mean platelet volume	Nudt19<tm1.1(KOMP)Vlcg>/Nudt19<tm1.1(KOMP)Vlcg>	C57BL/6N-Nudt19<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797690	M	MP:0003960	increased lean body mass	Oaf<tm1a(EUCOMM)Wtsi>/Oaf<tm1a(EUCOMM)Wtsi>	C57BL/6N-Oaf<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797691	F	MP:0000221	decreased leukocyte cell number	Ogn<tm1b(KOMP)Wtsi>/Ogn<tm1b(KOMP)Wtsi>	C57BL/6N-Ogn<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797691	F	MP:0001399	hyperactivity	Ogn<tm1b(KOMP)Wtsi>/Ogn<tm1b(KOMP)Wtsi>	C57BL/6N-Ogn<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797691	F	MP:0013279	increased fasting circulating glucose level	Ogn<tm1b(KOMP)Wtsi>/Ogn<tm1b(KOMP)Wtsi>	C57BL/6N-Ogn<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797691	F	MP:0010506	prolonged RR interval	Ogn<tm1b(KOMP)Wtsi>/Ogn<tm1b(KOMP)Wtsi>	C57BL/6N-Ogn<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797692	F	MP:0010024	increased total body fat amount	P3h1<tm1b(EUCOMM)Wtsi>/P3h1<tm1b(EUCOMM)Wtsi>	C57BL/6N-P3h1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797692	M	MP:0012000	abnormal limb position	P3h1<tm1b(EUCOMM)Wtsi>/P3h1<tm1b(EUCOMM)Wtsi>	C57BL/6N-P3h1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797692	M	MP:0001402	decreased locomotor activity	P3h1<tm1b(EUCOMM)Wtsi>/P3h1<tm1b(EUCOMM)Wtsi>	C57BL/6N-P3h1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797692	M	MP:0000759	abnormal skeletal muscle morphology	P3h1<tm1b(EUCOMM)Wtsi>/P3h1<tm1b(EUCOMM)Wtsi>	C57BL/6N-P3h1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797692	F	MP:0010506	prolonged RR interval	P3h1<tm1b(EUCOMM)Wtsi>/P3h1<tm1b(EUCOMM)Wtsi>	C57BL/6N-P3h1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797692	M	MP:0000266	abnormal heart morphology	P3h1<tm1b(EUCOMM)Wtsi>/P3h1<tm1b(EUCOMM)Wtsi>	C57BL/6N-P3h1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797692	F	MP:0001258	decreased body length	P3h1<tm1b(EUCOMM)Wtsi>/P3h1<tm1b(EUCOMM)Wtsi>	C57BL/6N-P3h1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797692	M	MP:0000274	enlarged heart	P3h1<tm1b(EUCOMM)Wtsi>/P3h1<tm1b(EUCOMM)Wtsi>	C57BL/6N-P3h1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797693	F	MP:0001926	female infertility	Padi6<tm1b(KOMP)Wtsi>/Padi6<tm1b(KOMP)Wtsi>	C57BL/6N-Padi6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797695	M	MP:0005293	impaired glucose tolerance	Pard6a<tm1.1(KOMP)Vlcg>/Pard6a<tm1.1(KOMP)Vlcg>	C57BL/6N-Pard6a<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797697	M	MP:0000274	enlarged heart	Pate2<tm1.1(KOMP)Vlcg>/Pate2<tm1.1(KOMP)Vlcg>	C57BL/6N-Pate2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797697	M	MP:0000266	abnormal heart morphology	Pate2<tm1.1(KOMP)Vlcg>/Pate2<tm1.1(KOMP)Vlcg>	C57BL/6N-Pate2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797698	M	MP:0002833	increased heart weight	Pate4<tm1.1(KOMP)Mbp>/Pate4<tm1.1(KOMP)Mbp>	C57BL/6N-Pate4<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5797698	F	MP:0001399	hyperactivity	Pate4<tm1.1(KOMP)Mbp>/Pate4<tm1.1(KOMP)Mbp>	C57BL/6N-Pate4<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5797698	F	MP:0013279	increased fasting circulating glucose level	Pate4<tm1.1(KOMP)Mbp>/Pate4<tm1.1(KOMP)Mbp>	C57BL/6N-Pate4<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:5797699	M	MP:0001146	abnormal testis morphology	Pcgf2<tm1b(KOMP)Mbp>/Pcgf2<+>	C57BL/6N-Pcgf2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5797699	F	MP:0000689	abnormal spleen morphology	Pcgf2<tm1b(KOMP)Mbp>/Pcgf2<+>	C57BL/6N-Pcgf2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5797699	F	MP:0010123	increased bone mineral content	Pcgf2<tm1b(KOMP)Mbp>/Pcgf2<+>	C57BL/6N-Pcgf2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5797699	M	MP:0001147	small testis	Pcgf2<tm1b(KOMP)Mbp>/Pcgf2<+>	C57BL/6N-Pcgf2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5797699	F	MP:0000692	small spleen	Pcgf2<tm1b(KOMP)Mbp>/Pcgf2<+>	C57BL/6N-Pcgf2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5797701	M	MP:0000274	enlarged heart	Pde6b<tm1b(KOMP)Wtsi>/Pde6b<tm1b(KOMP)Wtsi>	C57BL/6N-Pde6b<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797701	M	MP:0000266	abnormal heart morphology	Pde6b<tm1b(KOMP)Wtsi>/Pde6b<tm1b(KOMP)Wtsi>	C57BL/6N-Pde6b<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797702	M	MP:0003961	decreased lean body mass	Pde8a<tm1b(EUCOMM)Hmgu>/Pde8a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pde8a<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797702	M	MP:0010024	increased total body fat amount	Pde8a<tm1b(EUCOMM)Hmgu>/Pde8a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pde8a<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797703	M	MP:0003179	thrombocytopenia	Pdss2<tm1b(EUCOMM)Hmgu>/Pdss2<+>	C57BL/6N-Pdss2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797703	M	MP:0004609	vertebral fusion	Pdss2<tm1b(EUCOMM)Hmgu>/Pdss2<+>	C57BL/6N-Pdss2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797703	F	MP:0001304	cataract	Pdss2<tm1b(EUCOMM)Hmgu>/Pdss2<+>	C57BL/6N-Pdss2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797703	M	MP:0002100	abnormal tooth morphology	Pdss2<tm1b(EUCOMM)Hmgu>/Pdss2<+>	C57BL/6N-Pdss2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797704	M	MP:0000182	increased circulating LDL cholesterol level	Pdzk1<tm2b(EUCOMM)Wtsi>/Pdzk1<+>	C57BL/6N-Pdzk1<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797704	F	MP:0001556	increased circulating HDL cholesterol level	Pdzk1<tm2b(EUCOMM)Wtsi>/Pdzk1<+>	C57BL/6N-Pdzk1<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797705	M	MP:0002079	increased circulating insulin level	Pepd<tm1a(KOMP)Wtsi>/Pepd<tm1a(KOMP)Wtsi>	C57BL/6N-Pepd<tm1a(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797705	F	MP:0000218	increased leukocyte cell number	Pepd<tm1a(KOMP)Wtsi>/Pepd<tm1a(KOMP)Wtsi>	C57BL/6N-Pepd<tm1a(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797705	F	MP:0003795	abnormal bone structure	Pepd<tm1a(KOMP)Wtsi>/Pepd<tm1a(KOMP)Wtsi>	C57BL/6N-Pepd<tm1a(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797705	F	MP:0000063	decreased bone mineral density	Pepd<tm1a(KOMP)Wtsi>/Pepd<tm1a(KOMP)Wtsi>	C57BL/6N-Pepd<tm1a(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797705	F	MP:0005562	decreased mean corpuscular hemoglobin	Pepd<tm1a(KOMP)Wtsi>/Pepd<tm1a(KOMP)Wtsi>	C57BL/6N-Pepd<tm1a(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797705	F	MP:0002932	abnormal joint morphology	Pepd<tm1a(KOMP)Wtsi>/Pepd<tm1a(KOMP)Wtsi>	C57BL/6N-Pepd<tm1a(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797705	F	MP:0001325	abnormal retina morphology	Pepd<tm1a(KOMP)Wtsi>/Pepd<tm1a(KOMP)Wtsi>	C57BL/6N-Pepd<tm1a(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797705	F	MP:0010124	decreased bone mineral content	Pepd<tm1a(KOMP)Wtsi>/Pepd<tm1a(KOMP)Wtsi>	C57BL/6N-Pepd<tm1a(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797706	M	MP:0002631	abnormal epididymis morphology	Phf19<tm1.1(KOMP)Vlcg>/Phf19<tm1.1(KOMP)Vlcg>	C57BL/6N-Phf19<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797706	M	MP:0001147	small testis	Phf19<tm1.1(KOMP)Vlcg>/Phf19<tm1.1(KOMP)Vlcg>	C57BL/6N-Phf19<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797706	F	MP:0009709	hydrometra	Phf19<tm1.1(KOMP)Vlcg>/Phf19<tm1.1(KOMP)Vlcg>	C57BL/6N-Phf19<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797706	M	MP:0001146	abnormal testis morphology	Phf19<tm1.1(KOMP)Vlcg>/Phf19<tm1.1(KOMP)Vlcg>	C57BL/6N-Phf19<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797706	M	MP:0010379	decreased respiratory quotient	Phf19<tm1.1(KOMP)Vlcg>/Phf19<tm1.1(KOMP)Vlcg>	C57BL/6N-Phf19<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797706	M	MP:0004931	enlarged epididymis	Phf19<tm1.1(KOMP)Vlcg>/Phf19<tm1.1(KOMP)Vlcg>	C57BL/6N-Phf19<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797706	F	MP:0001120	abnormal uterus morphology	Phf19<tm1.1(KOMP)Vlcg>/Phf19<tm1.1(KOMP)Vlcg>	C57BL/6N-Phf19<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797708	M	MP:0002608	increased hematocrit	Phkg2<tm1.1(KOMP)Vlcg>/Phkg2<+>	C57BL/6N-Phkg2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797708	M	MP:0005564	increased hemoglobin content	Phkg2<tm1.1(KOMP)Vlcg>/Phkg2<+>	C57BL/6N-Phkg2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797708	M	MP:0003131	increased erythrocyte cell number	Phkg2<tm1.1(KOMP)Vlcg>/Phkg2<+>	C57BL/6N-Phkg2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797710	F	MP:0001891	hydrocephaly	Pigu<tm1b(EUCOMM)Hmgu>/Pigu<+>	C57BL/6N-Pigu<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5797711	M	MP:0000702	enlarged lymph nodes	Pik3c2a<tm1b(EUCOMM)Hmgu>/Pik3c2a<+>	C57BL/6N-Pik3c2a<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5797711	M	MP:0000219	increased neutrophil cell number	Pik3c2a<tm1b(EUCOMM)Hmgu>/Pik3c2a<+>	C57BL/6N-Pik3c2a<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5797711	M	MP:0001402	decreased locomotor activity	Pik3c2a<tm1b(EUCOMM)Hmgu>/Pik3c2a<+>	C57BL/6N-Pik3c2a<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5797711	M	MP:0005016	decreased lymphocyte cell number	Pik3c2a<tm1b(EUCOMM)Hmgu>/Pik3c2a<+>	C57BL/6N-Pik3c2a<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:5797712	M	MP:0013278	decreased fasting circulating glucose level	Pkn3<tm1.1(KOMP)Vlcg>/Pkn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Pkn3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797712	M	MP:0010052	increased grip strength	Pkn3<tm1.1(KOMP)Vlcg>/Pkn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Pkn3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797713	M	MP:0004151	decreased circulating iron level	Pkp4<tm1b(EUCOMM)Wtsi>/Pkp4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pkp4<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5797713	F	MP:0000063	decreased bone mineral density	Pkp4<tm1b(EUCOMM)Wtsi>/Pkp4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pkp4<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5797713	F	MP:0003795	abnormal bone structure	Pkp4<tm1b(EUCOMM)Wtsi>/Pkp4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pkp4<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5797713	F	MP:0001523	impaired righting response	Pkp4<tm1b(EUCOMM)Wtsi>/Pkp4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pkp4<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5797713	F	MP:0002968	increased circulating alkaline phosphatase level	Pkp4<tm1b(EUCOMM)Wtsi>/Pkp4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pkp4<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5797713	F	MP:0010124	decreased bone mineral content	Pkp4<tm1b(EUCOMM)Wtsi>/Pkp4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pkp4<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5797714	F	MP:0000266	abnormal heart morphology	Plat<tm1.1(KOMP)Vlcg>/Plat<tm1.1(KOMP)Vlcg>	C57BL/6N-Plat<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797714	M	MP:0001147	small testis	Plat<tm1.1(KOMP)Vlcg>/Plat<tm1.1(KOMP)Vlcg>	C57BL/6N-Plat<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797714	F	MP:0000274	enlarged heart	Plat<tm1.1(KOMP)Vlcg>/Plat<tm1.1(KOMP)Vlcg>	C57BL/6N-Plat<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797714	M	MP:0001146	abnormal testis morphology	Plat<tm1.1(KOMP)Vlcg>/Plat<tm1.1(KOMP)Vlcg>	C57BL/6N-Plat<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797715	F	MP:0001417	decreased exploration in new environment	Plau<tm1b(EUCOMM)Wtsi>/Plau<tm1b(EUCOMM)Wtsi>	C57BL/6N-Plau<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797715	M	MP:0000220	increased monocyte cell number	Plau<tm1b(EUCOMM)Wtsi>/Plau<tm1b(EUCOMM)Wtsi>	C57BL/6N-Plau<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797715	M	MP:0000219	increased neutrophil cell number	Plau<tm1b(EUCOMM)Wtsi>/Plau<tm1b(EUCOMM)Wtsi>	C57BL/6N-Plau<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797715	M	MP:0010053	decreased grip strength	Plau<tm1b(EUCOMM)Wtsi>/Plau<tm1b(EUCOMM)Wtsi>	C57BL/6N-Plau<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797716	M	MP:0010053	decreased grip strength	Plekha3<tm1.1(KOMP)Vlcg>/Plekha3<tm1.1(KOMP)Vlcg>	C57BL/6N-Plekha3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797716	F	MP:0001399	hyperactivity	Plekha3<tm1.1(KOMP)Vlcg>/Plekha3<tm1.1(KOMP)Vlcg>	C57BL/6N-Plekha3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797717	M	MP:0002135	abnormal kidney morphology	Plekha8<tm1b(KOMP)Wtsi>/Plekha8<tm1b(KOMP)Wtsi>	C57BL/6N-Plekha8<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797717	M	MP:0004931	enlarged epididymis	Plekha8<tm1b(KOMP)Wtsi>/Plekha8<tm1b(KOMP)Wtsi>	C57BL/6N-Plekha8<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797717	M	MP:0008528	polycystic kidney	Plekha8<tm1b(KOMP)Wtsi>/Plekha8<tm1b(KOMP)Wtsi>	C57BL/6N-Plekha8<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797717	M	MP:0000274	enlarged heart	Plekha8<tm1b(KOMP)Wtsi>/Plekha8<tm1b(KOMP)Wtsi>	C57BL/6N-Plekha8<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797717	M	MP:0000266	abnormal heart morphology	Plekha8<tm1b(KOMP)Wtsi>/Plekha8<tm1b(KOMP)Wtsi>	C57BL/6N-Plekha8<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797717	M	MP:0002631	abnormal epididymis morphology	Plekha8<tm1b(KOMP)Wtsi>/Plekha8<tm1b(KOMP)Wtsi>	C57BL/6N-Plekha8<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797719	M	MP:0001510	abnormal coat appearance	Plxnb3<tm1a(KOMP)Wtsi>/Y	C57BL/6N-Plxnb3<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797720	F	MP:0011960	abnormal eye anterior chamber depth	Podn<tm1b(KOMP)Wtsi>/Podn<tm1b(KOMP)Wtsi>	C57BL/6N-Podn<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5797720	F	MP:0011110	preweaning lethality, incomplete penetrance	Podn<tm1b(KOMP)Wtsi>/Podn<tm1b(KOMP)Wtsi>	C57BL/6N-Podn<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5797720	F	MP:0001319	irregularly shaped pupil	Podn<tm1b(KOMP)Wtsi>/Podn<tm1b(KOMP)Wtsi>	C57BL/6N-Podn<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5797722	F	MP:0000274	enlarged heart	Pou2f3<tm1.1(KOMP)Vlcg>/Pou2f3<tm1.1(KOMP)Vlcg>	C57BL/6N-Pou2f3<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797723	M	MP:0005016	decreased lymphocyte cell number	Ppbp<tm1.1(KOMP)Vlcg>/Ppbp<tm1.1(KOMP)Vlcg>	C57BL/6N-Ppbp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797723	M	MP:0004952	increased spleen weight	Ppbp<tm1.1(KOMP)Vlcg>/Ppbp<tm1.1(KOMP)Vlcg>	C57BL/6N-Ppbp<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797724	M	MP:0001410	head bobbing	Ppfia2<tm1b(EUCOMM)Hmgu>/Ppfia2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppfia2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797724	F	MP:0002792	abnormal retina vasculature morphology	Ppfia2<tm1b(EUCOMM)Hmgu>/Ppfia2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppfia2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797724	F	MP:0001406	abnormal gait	Ppfia2<tm1b(EUCOMM)Hmgu>/Ppfia2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppfia2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797724	F	MP:0010097	abnormal retina blood vessel morphology	Ppfia2<tm1b(EUCOMM)Hmgu>/Ppfia2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppfia2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797724	F	MP:0008259	abnormal optic disk morphology	Ppfia2<tm1b(EUCOMM)Hmgu>/Ppfia2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppfia2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797725	F	MP:0001402	decreased locomotor activity	Ppp1cc<tm1b(EUCOMM)Wtsi>/Ppp1cc<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ppp1cc<tm1b(EUCOMM)Wtsi>/Nju	N	MGI:5576271
MGI:5797726	F	MP:0010068	decreased red blood cell distribution width	Ppp1r14d<tm1b(KOMP)Wtsi>/Ppp1r14d<tm1b(KOMP)Wtsi>	C57BL/6N-Ppp1r14d<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797726	M	MP:0002753	dilated heart left ventricle	Ppp1r14d<tm1b(KOMP)Wtsi>/Ppp1r14d<tm1b(KOMP)Wtsi>	C57BL/6N-Ppp1r14d<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797727	M	MP:0005633	increased circulating sodium level	Ppp1r26<tm1.1(KOMP)Vlcg>/Ppp1r26<tm1.1(KOMP)Vlcg>	C57BL/6N-Ppp1r26<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797728	F	MP:0001303	abnormal lens morphology	Ppp1r35<tm1.1(KOMP)Vlcg>/Ppp1r35<+>	C57BL/6N-Ppp1r35<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797728	F	MP:0003020	decreased circulating chloride level	Ppp1r35<tm1.1(KOMP)Vlcg>/Ppp1r35<+>	C57BL/6N-Ppp1r35<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797730	M	MP:0010067	increased red blood cell distribution width	Ppp3r2<tm1.1(KOMP)Vlcg>/Ppp3r2<tm1.1(KOMP)Vlcg>	C57BL/6N-Ppp3r2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797730	M	MP:0001925	male infertility	Ppp3r2<tm1.1(KOMP)Vlcg>/Ppp3r2<tm1.1(KOMP)Vlcg>	C57BL/6N-Ppp3r2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797732	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Prf1<tm1.1(KOMP)Vlcg>/Prf1<tm1.1(KOMP)Vlcg>	C57BL/6N-Prf1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797733	M	MP:0002060	abnormal skin morphology	Prg3<tm1.1(KOMP)Vlcg>/Prg3<tm1.1(KOMP)Vlcg>	C57BL/6N-Prg3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797733	M	MP:0000266	abnormal heart morphology	Prg3<tm1.1(KOMP)Vlcg>/Prg3<tm1.1(KOMP)Vlcg>	C57BL/6N-Prg3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797733	M	MP:0000274	enlarged heart	Prg3<tm1.1(KOMP)Vlcg>/Prg3<tm1.1(KOMP)Vlcg>	C57BL/6N-Prg3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797735	M	MP:0001147	small testis	Prkcq<tm1.1(KOMP)Vlcg>/Prkcq<tm1.1(KOMP)Vlcg>	C57BL/6N-Prkcq<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797735	M	MP:0001925	male infertility	Prkcq<tm1.1(KOMP)Vlcg>/Prkcq<tm1.1(KOMP)Vlcg>	C57BL/6N-Prkcq<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797735	M	MP:0001146	abnormal testis morphology	Prkcq<tm1.1(KOMP)Vlcg>/Prkcq<tm1.1(KOMP)Vlcg>	C57BL/6N-Prkcq<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797736	F	MP:0000691	enlarged spleen	Prkg1<tm1b(KOMP)Wtsi>/Prkg1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkg1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797736	F	MP:0003271	abnormal duodenum morphology	Prkg1<tm1b(KOMP)Wtsi>/Prkg1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkg1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797739	F	MP:0000274	enlarged heart	Prss1<tm1.1(KOMP)Vlcg>/Prss1<tm1.1(KOMP)Vlcg>	C57BL/6N-Prss1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797741	M	MP:0000689	abnormal spleen morphology	Psca<tm1b(EUCOMM)Hmgu>/Psca<tm1b(EUCOMM)Hmgu>	C57BL/6N-Psca<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5797743	M	MP:0003960	increased lean body mass	Ptchd1<tm1b(KOMP)IcsOrl>/Y	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797743	M	MP:0001399	hyperactivity	Ptchd1<tm1b(KOMP)IcsOrl>/Y	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797743	M	MP:0005655	increased aggression	Ptchd1<tm1b(KOMP)IcsOrl>/Y	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797743	M	MP:0001392	abnormal locomotor behavior	Ptchd1<tm1b(KOMP)IcsOrl>/Y	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797743	M	MP:0001529	abnormal vocalization	Ptchd1<tm1b(KOMP)IcsOrl>/Y	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797743	M	MP:0001415	increased exploration in new environment	Ptchd1<tm1b(KOMP)IcsOrl>/Y	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797743	M	MP:0004738	abnormal auditory brainstem response	Ptchd1<tm1b(KOMP)IcsOrl>/Y	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797743	M	MP:0000063	decreased bone mineral density	Ptchd1<tm1b(KOMP)IcsOrl>/Y	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797743	M	MP:0002574	increased vertical activity	Ptchd1<tm1b(KOMP)IcsOrl>/Y	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797743	M	MP:0000689	abnormal spleen morphology	Ptchd1<tm1b(KOMP)IcsOrl>/Y	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797744	F	MP:0005553	increased circulating creatinine level	Ptchd1<tm1b(KOMP)IcsOrl>/Ptchd1<tm1b(KOMP)IcsOrl>	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797744	F	MP:0001469	abnormal contextual conditioning behavior	Ptchd1<tm1b(KOMP)IcsOrl>/Ptchd1<tm1b(KOMP)IcsOrl>	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797744	F	MP:0002875	decreased erythrocyte cell number	Ptchd1<tm1b(KOMP)IcsOrl>/Ptchd1<tm1b(KOMP)IcsOrl>	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797744	F	MP:0001399	hyperactivity	Ptchd1<tm1b(KOMP)IcsOrl>/Ptchd1<tm1b(KOMP)IcsOrl>	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797744	F	MP:0001454	abnormal cued conditioning behavior	Ptchd1<tm1b(KOMP)IcsOrl>/Ptchd1<tm1b(KOMP)IcsOrl>	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797744	F	MP:0001415	increased exploration in new environment	Ptchd1<tm1b(KOMP)IcsOrl>/Ptchd1<tm1b(KOMP)IcsOrl>	C57BL/6N-Ptchd1<tm1b(KOMP)IcsOrl>/Ics	N	MGI:5576271
MGI:5797749	F	MP:0001513	limb grasping	Ptpn20<tm1b(KOMP)Wtsi>/Ptpn20<tm1b(KOMP)Wtsi>	C57BL/6N-Ptpn20<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797749	M	MP:0003019	increased circulating chloride level	Ptpn20<tm1b(KOMP)Wtsi>/Ptpn20<tm1b(KOMP)Wtsi>	C57BL/6N-Ptpn20<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797749	F	MP:0001303	abnormal lens morphology	Ptpn20<tm1b(KOMP)Wtsi>/Ptpn20<tm1b(KOMP)Wtsi>	C57BL/6N-Ptpn20<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797751	F	MP:0000274	enlarged heart	Ptprs<tm1b(KOMP)Mbp>/Ptprs<+>	C57BL/6N-Ptprs<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5797751	F	MP:0000266	abnormal heart morphology	Ptprs<tm1b(KOMP)Mbp>/Ptprs<+>	C57BL/6N-Ptprs<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5797751	F	MP:0009709	hydrometra	Ptprs<tm1b(KOMP)Mbp>/Ptprs<+>	C57BL/6N-Ptprs<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5797751	F	MP:0001120	abnormal uterus morphology	Ptprs<tm1b(KOMP)Mbp>/Ptprs<+>	C57BL/6N-Ptprs<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5797751	M	MP:0002599	increased mean platelet volume	Ptprs<tm1b(KOMP)Mbp>/Ptprs<+>	C57BL/6N-Ptprs<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5797752	F	MP:0001289	persistence of hyaloid vascular system	Ptpru<tm1.1(KOMP)Vlcg>/Ptpru<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpru<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797752	F	MP:0002574	increased vertical activity	Ptpru<tm1.1(KOMP)Vlcg>/Ptpru<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptpru<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797753	F	MP:0013279	increased fasting circulating glucose level	Pycr2<tm1a(EUCOMM)Wtsi>/Pycr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pycr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797753	M	MP:0000063	decreased bone mineral density	Pycr2<tm1a(EUCOMM)Wtsi>/Pycr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pycr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797753	F	MP:0005561	increased mean corpuscular hemoglobin	Pycr2<tm1a(EUCOMM)Wtsi>/Pycr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pycr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797753	F	MP:0001512	trunk curl	Pycr2<tm1a(EUCOMM)Wtsi>/Pycr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pycr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797753	M	MP:0013026	decreased Ly6C low monocyte number	Pycr2<tm1a(EUCOMM)Wtsi>/Pycr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pycr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797753	M	MP:0000223	decreased monocyte cell number	Pycr2<tm1a(EUCOMM)Wtsi>/Pycr2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pycr2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797754	F	MP:0001289	persistence of hyaloid vascular system	R3hcc1l<tm1b(KOMP)Wtsi>/R3hcc1l<tm1b(KOMP)Wtsi>	C57BL/6N-R3hcc1l<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797755	M	MP:0001147	small testis	R3hdm1<tm1b(EUCOMM)Wtsi>/R3hdm1<tm1b(EUCOMM)Wtsi>	C57BL/6N-R3hdm1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797755	M	MP:0001146	abnormal testis morphology	R3hdm1<tm1b(EUCOMM)Wtsi>/R3hdm1<tm1b(EUCOMM)Wtsi>	C57BL/6N-R3hdm1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5797756	M	MP:0005560	decreased circulating glucose level	Rab11fip5<tm1.1(KOMP)Vlcg>/Rab11fip5<tm1.1(KOMP)Vlcg>	C57BL/6N-Rab11fip5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797756	F	MP:0010053	decreased grip strength	Rab11fip5<tm1.1(KOMP)Vlcg>/Rab11fip5<tm1.1(KOMP)Vlcg>	C57BL/6N-Rab11fip5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797759	F	MP:0010052	increased grip strength	Rab32<tm1b(KOMP)Wtsi>/Rab32<+>	C57BL/6N-Rab32<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797760	F	MP:0011396	abnormal sleep behavior	Rabac1<tm1.1(KOMP)Vlcg>/Rabac1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rabac1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797760	F	MP:0001303	abnormal lens morphology	Rabac1<tm1.1(KOMP)Vlcg>/Rabac1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rabac1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797761	M	MP:0005564	increased hemoglobin content	Rabggta<tm1.1(KOMP)Vlcg>/Rabggta<+>	C57BL/6N-Rabggta<tm1.1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5797761	F	MP:0000222	decreased neutrophil cell number	Rabggta<tm1.1(KOMP)Vlcg>/Rabggta<+>	C57BL/6N-Rabggta<tm1.1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5797763	M	MP:0005344	increased circulating bilirubin level	Rad1<tm1b(KOMP)Wtsi>/Rad1<+>	C57BL/6N-Rad1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797763	M	MP:0004151	decreased circulating iron level	Rad1<tm1b(KOMP)Wtsi>/Rad1<+>	C57BL/6N-Rad1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797763	M	MP:0000186	decreased circulating HDL cholesterol level	Rad1<tm1b(KOMP)Wtsi>/Rad1<+>	C57BL/6N-Rad1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797763	M	MP:0003131	increased erythrocyte cell number	Rad1<tm1b(KOMP)Wtsi>/Rad1<+>	C57BL/6N-Rad1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797763	M	MP:0002608	increased hematocrit	Rad1<tm1b(KOMP)Wtsi>/Rad1<+>	C57BL/6N-Rad1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797763	F	MP:0013279	increased fasting circulating glucose level	Rad1<tm1b(KOMP)Wtsi>/Rad1<+>	C57BL/6N-Rad1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797763	F	MP:0003795	abnormal bone structure	Rad1<tm1b(KOMP)Wtsi>/Rad1<+>	C57BL/6N-Rad1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797763	M	MP:0001303	abnormal lens morphology	Rad1<tm1b(KOMP)Wtsi>/Rad1<+>	C57BL/6N-Rad1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797764	F	MP:0011960	abnormal eye anterior chamber depth	Rad9a<tm1.1(KOMP)Wtsi>/Rad9a<+>	C57BL/6N-Rad9a<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5797765	M	MP:0001304	cataract	Raf1<tm1b(EUCOMM)Wtsi>/Raf1<+>	C57BL/6N-Raf1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797765	M	MP:0001303	abnormal lens morphology	Raf1<tm1b(EUCOMM)Wtsi>/Raf1<+>	C57BL/6N-Raf1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797766	M	MP:0004151	decreased circulating iron level	Rap2b<tm1.1(KOMP)Vlcg>/Rap2b<tm1.1(KOMP)Vlcg>	C57BL/6N-Rap2b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797766	M	MP:0004924	abnormal behavior	Rap2b<tm1.1(KOMP)Vlcg>/Rap2b<tm1.1(KOMP)Vlcg>	C57BL/6N-Rap2b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797766	M	MP:0005560	decreased circulating glucose level	Rap2b<tm1.1(KOMP)Vlcg>/Rap2b<tm1.1(KOMP)Vlcg>	C57BL/6N-Rap2b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797766	M	MP:0020870	decreased thigmotaxis	Rap2b<tm1.1(KOMP)Vlcg>/Rap2b<tm1.1(KOMP)Vlcg>	C57BL/6N-Rap2b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797767	F	MP:0004924	abnormal behavior	Rasa1<tm1b(EUCOMM)Hmgu>/Rasa1<+>	C57BL/6N-Rasa1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797767	F	MP:0003179	thrombocytopenia	Rasa1<tm1b(EUCOMM)Hmgu>/Rasa1<+>	C57BL/6N-Rasa1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797767	F	MP:0005560	decreased circulating glucose level	Rasa1<tm1b(EUCOMM)Hmgu>/Rasa1<+>	C57BL/6N-Rasa1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797767	F	MP:0000198	decreased circulating phosphate level	Rasa1<tm1b(EUCOMM)Hmgu>/Rasa1<+>	C57BL/6N-Rasa1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797767	M	MP:0002792	abnormal retina vasculature morphology	Rasa1<tm1b(EUCOMM)Hmgu>/Rasa1<+>	C57BL/6N-Rasa1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797767	F	MP:0005561	increased mean corpuscular hemoglobin	Rasa1<tm1b(EUCOMM)Hmgu>/Rasa1<+>	C57BL/6N-Rasa1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797768	M	MP:0006358	absent pinna reflex	Rasal2<tm1a(EUCOMM)Wtsi>/Rasal2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Rasal2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797768	M	MP:0002073	abnormal hair growth	Rasal2<tm1a(EUCOMM)Wtsi>/Rasal2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Rasal2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797768	M	MP:0001510	abnormal coat appearance	Rasal2<tm1a(EUCOMM)Wtsi>/Rasal2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Rasal2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797769	F	MP:0002599	increased mean platelet volume	Rasgrp4<tm2a(KOMP)Wtsi>/Rasgrp4<tm2a(KOMP)Wtsi>	C57BL/6N-Rasgrp4<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797770	M	MP:0000266	abnormal heart morphology	Rassf8<tm1.1(KOMP)Vlcg>/Rassf8<+>	C57BL/6N-Rassf8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797770	F	MP:0000367	abnormal coat/ hair morphology	Rassf8<tm1.1(KOMP)Vlcg>/Rassf8<+>	C57BL/6N-Rassf8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797770	M	MP:0000274	enlarged heart	Rassf8<tm1.1(KOMP)Vlcg>/Rassf8<+>	C57BL/6N-Rassf8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797770	M	MP:0001147	small testis	Rassf8<tm1.1(KOMP)Vlcg>/Rassf8<+>	C57BL/6N-Rassf8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797770	M	MP:0001146	abnormal testis morphology	Rassf8<tm1.1(KOMP)Vlcg>/Rassf8<+>	C57BL/6N-Rassf8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797773	F	MP:0002874	decreased hemoglobin content	Rhpn1<tm1b(KOMP)Wtsi>/Rhpn1<tm1b(KOMP)Wtsi>	C57BL/6N-Rhpn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797773	M	MP:0002981	increased liver weight	Rhpn1<tm1b(KOMP)Wtsi>/Rhpn1<tm1b(KOMP)Wtsi>	C57BL/6N-Rhpn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797773	F	MP:0002135	abnormal kidney morphology	Rhpn1<tm1b(KOMP)Wtsi>/Rhpn1<tm1b(KOMP)Wtsi>	C57BL/6N-Rhpn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797773	M	MP:0001556	increased circulating HDL cholesterol level	Rhpn1<tm1b(KOMP)Wtsi>/Rhpn1<tm1b(KOMP)Wtsi>	C57BL/6N-Rhpn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797773	F	MP:0002599	increased mean platelet volume	Rhpn1<tm1b(KOMP)Wtsi>/Rhpn1<tm1b(KOMP)Wtsi>	C57BL/6N-Rhpn1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797774	M	MP:0001284	absent vibrissae	Riiad1<tm1b(KOMP)Wtsi>/Riiad1<+>	C57BL/6N-Riiad1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797775	F	MP:0013279	increased fasting circulating glucose level	Rin3<tm1.1(KOMP)Vlcg>/Rin3<tm1.1(KOMP)Vlcg>	C57BL/6N-Rin3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797775	M	MP:0011436	decreased urine magnesium level	Rin3<tm1.1(KOMP)Vlcg>/Rin3<tm1.1(KOMP)Vlcg>	C57BL/6N-Rin3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797775	F	MP:0004151	decreased circulating iron level	Rin3<tm1.1(KOMP)Vlcg>/Rin3<tm1.1(KOMP)Vlcg>	C57BL/6N-Rin3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797776	M	MP:0002941	increased circulating alanine transaminase level	Rnasek<tm1b(EUCOMM)Wtsi>/Rnasek<+>	C57BL/6N-Rnasek<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797777	M	MP:0012362	increased large unstained cell number	Rnd3<tm1b(EUCOMM)Hmgu>/Rnd3<+>	C57BL/6N-Rnd3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797777	M	MP:0010053	decreased grip strength	Rnd3<tm1b(EUCOMM)Hmgu>/Rnd3<+>	C57BL/6N-Rnd3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797777	F	MP:0008528	polycystic kidney	Rnd3<tm1b(EUCOMM)Hmgu>/Rnd3<+>	C57BL/6N-Rnd3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797777	F	MP:0000274	enlarged heart	Rnd3<tm1b(EUCOMM)Hmgu>/Rnd3<+>	C57BL/6N-Rnd3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797778	M	MP:0005344	increased circulating bilirubin level	Rnf125<tm1a(EUCOMM)Hmgu>/Rnf125<tm1a(EUCOMM)Hmgu>	C57BL/6N-Rnf125<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:5797779	F	MP:0012000	abnormal limb position	Rnf13<tm1.1(KOMP)Vlcg>/Rnf13<tm1.1(KOMP)Vlcg>	C57BL/6N-Rnf13<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797779	M	MP:0005561	increased mean corpuscular hemoglobin	Rnf13<tm1.1(KOMP)Vlcg>/Rnf13<tm1.1(KOMP)Vlcg>	C57BL/6N-Rnf13<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797779	F	MP:0000556	abnormal hindlimb morphology	Rnf13<tm1.1(KOMP)Vlcg>/Rnf13<tm1.1(KOMP)Vlcg>	C57BL/6N-Rnf13<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797780	M	MP:0001303	abnormal lens morphology	Rnf157<tm1b(EUCOMM)Wtsi>/Rnf157<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rnf157<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797780	M	MP:0008806	increased circulating amylase level	Rnf157<tm1b(EUCOMM)Wtsi>/Rnf157<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rnf157<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797780	M	MP:0001304	cataract	Rnf157<tm1b(EUCOMM)Wtsi>/Rnf157<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rnf157<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797783	F	MP:0011239	abnormal skin coloration	Rps19bp1<tm1.1(KOMP)Wtsi>/Rps19bp1<+>	C57BL/6N-Rps19bp1<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5797783	F	MP:0000689	abnormal spleen morphology	Rps19bp1<tm1.1(KOMP)Wtsi>/Rps19bp1<+>	C57BL/6N-Rps19bp1<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5797784	M	MP:0005633	increased circulating sodium level	Rps6kl1<tm1.1(KOMP)Vlcg>/Rps6kl1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rps6kl1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797784	M	MP:0004151	decreased circulating iron level	Rps6kl1<tm1.1(KOMP)Vlcg>/Rps6kl1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rps6kl1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797784	M	MP:0005560	decreased circulating glucose level	Rps6kl1<tm1.1(KOMP)Vlcg>/Rps6kl1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rps6kl1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797786	M	MP:0003179	thrombocytopenia	Rwdd1<tm1b(KOMP)Wtsi>/Rwdd1<tm1b(KOMP)Wtsi>	C57BL/6N-Rwdd1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797786	F	MP:0010124	decreased bone mineral content	Rwdd1<tm1b(KOMP)Wtsi>/Rwdd1<tm1b(KOMP)Wtsi>	C57BL/6N-Rwdd1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797786	M	MP:0001552	increased circulating triglyceride level	Rwdd1<tm1b(KOMP)Wtsi>/Rwdd1<tm1b(KOMP)Wtsi>	C57BL/6N-Rwdd1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797786	M	MP:0004974	decreased regulatory T cell number	Rwdd1<tm1b(KOMP)Wtsi>/Rwdd1<tm1b(KOMP)Wtsi>	C57BL/6N-Rwdd1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797786	F	MP:0010024	increased total body fat amount	Rwdd1<tm1b(KOMP)Wtsi>/Rwdd1<tm1b(KOMP)Wtsi>	C57BL/6N-Rwdd1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797786	M	MP:0005344	increased circulating bilirubin level	Rwdd1<tm1b(KOMP)Wtsi>/Rwdd1<tm1b(KOMP)Wtsi>	C57BL/6N-Rwdd1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797786	F	MP:0003795	abnormal bone structure	Rwdd1<tm1b(KOMP)Wtsi>/Rwdd1<tm1b(KOMP)Wtsi>	C57BL/6N-Rwdd1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797786	F	MP:0001325	abnormal retina morphology	Rwdd1<tm1b(KOMP)Wtsi>/Rwdd1<tm1b(KOMP)Wtsi>	C57BL/6N-Rwdd1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797787	F	MP:0011436	decreased urine magnesium level	Rxfp4<tm1.1(KOMP)Vlcg>/Rxfp4<tm1.1(KOMP)Vlcg>	C57BL/6N-Rxfp4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797787	M	MP:0003179	thrombocytopenia	Rxfp4<tm1.1(KOMP)Vlcg>/Rxfp4<tm1.1(KOMP)Vlcg>	C57BL/6N-Rxfp4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797788	F	MP:0004952	increased spleen weight	Ryr1<tm1b(EUCOMM)Hmgu>/Ryr1<+>	C57BL/6N-Ryr1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797788	M	MP:0010378	increased respiratory quotient	Ryr1<tm1b(EUCOMM)Hmgu>/Ryr1<+>	C57BL/6N-Ryr1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797789	M	MP:0001399	hyperactivity	Sacm1l<tm1b(KOMP)Wtsi>/Sacm1l<+>	C57BL/6N-Sacm1l<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797789	M	MP:0020870	decreased thigmotaxis	Sacm1l<tm1b(KOMP)Wtsi>/Sacm1l<+>	C57BL/6N-Sacm1l<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797789	M	MP:0002631	abnormal epididymis morphology	Sacm1l<tm1b(KOMP)Wtsi>/Sacm1l<+>	C57BL/6N-Sacm1l<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797789	M	MP:0001146	abnormal testis morphology	Sacm1l<tm1b(KOMP)Wtsi>/Sacm1l<+>	C57BL/6N-Sacm1l<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797789	M	MP:0001147	small testis	Sacm1l<tm1b(KOMP)Wtsi>/Sacm1l<+>	C57BL/6N-Sacm1l<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797789	M	MP:0004924	abnormal behavior	Sacm1l<tm1b(KOMP)Wtsi>/Sacm1l<+>	C57BL/6N-Sacm1l<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797789	M	MP:0004931	enlarged epididymis	Sacm1l<tm1b(KOMP)Wtsi>/Sacm1l<+>	C57BL/6N-Sacm1l<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797790	M	MP:0000062	increased bone mineral density	Sapcd1<tm1.1(KOMP)Vlcg>/Sapcd1<+>	C57BL/6N-Sapcd1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797791	F	MP:0001399	hyperactivity	Satb1<tm1b(EUCOMM)Hmgu>/Satb1<+>	C57BL/6N-Satb1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797791	F	MP:0001415	increased exploration in new environment	Satb1<tm1b(EUCOMM)Hmgu>/Satb1<+>	C57BL/6N-Satb1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797791	M	MP:0010123	increased bone mineral content	Satb1<tm1b(EUCOMM)Hmgu>/Satb1<+>	C57BL/6N-Satb1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797793	F	MP:0001325	abnormal retina morphology	Scrib<tm1b(NCOM)Mfgc>/Scrib<+>	C57BL/6N-Scrib<tm1a(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797793	F	MP:0001406	abnormal gait	Scrib<tm1b(NCOM)Mfgc>/Scrib<+>	C57BL/6N-Scrib<tm1a(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797794	F	MP:0001722	pale yolk sac	Scrib<tm1b(NCOM)Mfgc>/Scrib<tm1b(NCOM)Mfgc>	C57BL/6N-Scrib<tm1a(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797794	F	MP:0000288	abnormal pericardium morphology	Scrib<tm1b(NCOM)Mfgc>/Scrib<tm1b(NCOM)Mfgc>	C57BL/6N-Scrib<tm1a(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797794	F	MP:0004258	abnormal placenta size	Scrib<tm1b(NCOM)Mfgc>/Scrib<tm1b(NCOM)Mfgc>	C57BL/6N-Scrib<tm1a(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797796	M	MP:0002546	mydriasis	Sdc4<tm2b(KOMP)Wtsi>/Sdc4<+>	C57BL/6N-Sdc4<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797797	M	MP:0005016	decreased lymphocyte cell number	Sdc4<tm2b(KOMP)Wtsi>/Sdc4<tm2b(KOMP)Wtsi>	C57BL/6N-Sdc4<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797797	F	MP:0005419	decreased circulating serum albumin level	Sdc4<tm2b(KOMP)Wtsi>/Sdc4<tm2b(KOMP)Wtsi>	C57BL/6N-Sdc4<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797797	F	MP:0008935	decreased mean platelet volume	Sdc4<tm2b(KOMP)Wtsi>/Sdc4<tm2b(KOMP)Wtsi>	C57BL/6N-Sdc4<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797797	M	MP:0010067	increased red blood cell distribution width	Sdc4<tm2b(KOMP)Wtsi>/Sdc4<tm2b(KOMP)Wtsi>	C57BL/6N-Sdc4<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797797	M	MP:0000219	increased neutrophil cell number	Sdc4<tm2b(KOMP)Wtsi>/Sdc4<tm2b(KOMP)Wtsi>	C57BL/6N-Sdc4<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797798	M	MP:0004609	vertebral fusion	Sel1l<tm1e(KOMP)Wtsi>/Sel1l<+>	C57BL/6N-Sel1l<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797799	F	MP:0004952	increased spleen weight	Sell<tm1b(EUCOMM)Hmgu>/Sell<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sell<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797801	F	MP:0002764	short tibia	Serpinb12<tm1b(KOMP)Wtsi>/Serpinb12<tm1b(KOMP)Wtsi>	C57BL/6N-Serpinb12<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797801	F	MP:0001410	head bobbing	Serpinb12<tm1b(KOMP)Wtsi>/Serpinb12<tm1b(KOMP)Wtsi>	C57BL/6N-Serpinb12<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5797802	M	MP:0005179	decreased circulating cholesterol level	Setbp1<tm1b(EUCOMM)Wtsi>/Setbp1<+>	C57BL/6N-Setbp1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797804	M	MP:0010392	prolonged QRS complex duration	Setd2<tm1b(NCOM)Mfgc>/Setd2<tm1b(NCOM)Mfgc>	C57BL/6N-Setd2<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797805	F	MP:0000062	increased bone mineral density	Setd3<tm1.1(NCOM)Mfgc>/Setd3<tm1.1(NCOM)Mfgc>	C57BL/6N-Setd3<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797805	M	MP:0001258	decreased body length	Setd3<tm1.1(NCOM)Mfgc>/Setd3<tm1.1(NCOM)Mfgc>	C57BL/6N-Setd3<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797805	M	MP:0020422	decreased freezing behavior	Setd3<tm1.1(NCOM)Mfgc>/Setd3<tm1.1(NCOM)Mfgc>	C57BL/6N-Setd3<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797805	M	MP:0001399	hyperactivity	Setd3<tm1.1(NCOM)Mfgc>/Setd3<tm1.1(NCOM)Mfgc>	C57BL/6N-Setd3<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797805	F	MP:0010123	increased bone mineral content	Setd3<tm1.1(NCOM)Mfgc>/Setd3<tm1.1(NCOM)Mfgc>	C57BL/6N-Setd3<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797805	F	MP:0009709	hydrometra	Setd3<tm1.1(NCOM)Mfgc>/Setd3<tm1.1(NCOM)Mfgc>	C57BL/6N-Setd3<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797805	F	MP:0001944	abnormal pancreas morphology	Setd3<tm1.1(NCOM)Mfgc>/Setd3<tm1.1(NCOM)Mfgc>	C57BL/6N-Setd3<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797805	M	MP:0005013	increased lymphocyte cell number	Setd3<tm1.1(NCOM)Mfgc>/Setd3<tm1.1(NCOM)Mfgc>	C57BL/6N-Setd3<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797805	M	MP:0002059	abnormal seminal vesicle morphology	Setd3<tm1.1(NCOM)Mfgc>/Setd3<tm1.1(NCOM)Mfgc>	C57BL/6N-Setd3<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797805	M	MP:0001147	small testis	Setd3<tm1.1(NCOM)Mfgc>/Setd3<tm1.1(NCOM)Mfgc>	C57BL/6N-Setd3<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797805	M	MP:0009142	decreased prepulse inhibition	Setd3<tm1.1(NCOM)Mfgc>/Setd3<tm1.1(NCOM)Mfgc>	C57BL/6N-Setd3<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797807	M	MP:0004931	enlarged epididymis	Sgpl1<tm1.1(KOMP)Vlcg>/Sgpl1<+>	C57BL/6N-Sgpl1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797807	M	MP:0002631	abnormal epididymis morphology	Sgpl1<tm1.1(KOMP)Vlcg>/Sgpl1<+>	C57BL/6N-Sgpl1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797807	M	MP:0001146	abnormal testis morphology	Sgpl1<tm1.1(KOMP)Vlcg>/Sgpl1<+>	C57BL/6N-Sgpl1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797807	M	MP:0001147	small testis	Sgpl1<tm1.1(KOMP)Vlcg>/Sgpl1<+>	C57BL/6N-Sgpl1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797808	F	MP:0001258	decreased body length	Sgta<tm1b(KOMP)Mbp>/Sgta<tm1b(KOMP)Mbp>	C57BL/6N-Sgta<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5797808	F	MP:0000208	decreased hematocrit	Sgta<tm1b(KOMP)Mbp>/Sgta<tm1b(KOMP)Mbp>	C57BL/6N-Sgta<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5797810	M	MP:0001314	cornea opacity	Shroom4<tm1.1(NCOM)Mfgc>/Y	C57BL/6N-Shroom4<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797812	M	MP:0000598	abnormal liver morphology	Sidt1<tm1.1(KOMP)Vlcg>/Sidt1<tm1.1(KOMP)Vlcg>	C57BL/6N-Sidt1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797812	M	MP:0002339	abnormal lymph node morphology	Sidt1<tm1.1(KOMP)Vlcg>/Sidt1<tm1.1(KOMP)Vlcg>	C57BL/6N-Sidt1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797814	F	MP:0010090	increased circulating creatine kinase level	Sirt3<tm1b(EUCOMM)Wtsi>/Sirt3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sirt3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797814	M	MP:0001406	abnormal gait	Sirt3<tm1b(EUCOMM)Wtsi>/Sirt3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sirt3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797814	M	MP:0002941	increased circulating alanine transaminase level	Sirt3<tm1b(EUCOMM)Wtsi>/Sirt3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sirt3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797815	F	MP:0003020	decreased circulating chloride level	Skic2<tm2b(EUCOMM)Wtsi>/Skic2<+>	C57BL/6N-Skic2<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5797815	F	MP:0005568	increased circulating total protein level	Skic2<tm2b(EUCOMM)Wtsi>/Skic2<+>	C57BL/6N-Skic2<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5797817	F	MP:0004122	abnormal sinus arrhythmia	Slc29a1<tm2b(NCOM)Mfgc>/Slc29a1<tm2b(NCOM)Mfgc>	C57BL/6N-Slc29a1<tm2b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797817	F	MP:0002092	abnormal eye morphology	Slc29a1<tm2b(NCOM)Mfgc>/Slc29a1<tm2b(NCOM)Mfgc>	C57BL/6N-Slc29a1<tm2b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797817	M	MP:0005292	improved glucose tolerance	Slc29a1<tm2b(NCOM)Mfgc>/Slc29a1<tm2b(NCOM)Mfgc>	C57BL/6N-Slc29a1<tm2b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797817	F	MP:0002764	short tibia	Slc29a1<tm2b(NCOM)Mfgc>/Slc29a1<tm2b(NCOM)Mfgc>	C57BL/6N-Slc29a1<tm2b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797817	F	MP:0010506	prolonged RR interval	Slc29a1<tm2b(NCOM)Mfgc>/Slc29a1<tm2b(NCOM)Mfgc>	C57BL/6N-Slc29a1<tm2b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797817	F	MP:0005333	decreased heart rate	Slc29a1<tm2b(NCOM)Mfgc>/Slc29a1<tm2b(NCOM)Mfgc>	C57BL/6N-Slc29a1<tm2b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797817	F	MP:0000063	decreased bone mineral density	Slc29a1<tm2b(NCOM)Mfgc>/Slc29a1<tm2b(NCOM)Mfgc>	C57BL/6N-Slc29a1<tm2b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797817	F	MP:0009142	decreased prepulse inhibition	Slc29a1<tm2b(NCOM)Mfgc>/Slc29a1<tm2b(NCOM)Mfgc>	C57BL/6N-Slc29a1<tm2b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797818	M	MP:0002833	increased heart weight	Slc35b4<tm1.1(KOMP)Vlcg>/Slc35b4<+>	C57BL/6N-Slc35b4<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5797818	M	MP:0000274	enlarged heart	Slc35b4<tm1.1(KOMP)Vlcg>/Slc35b4<+>	C57BL/6N-Slc35b4<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5797818	M	MP:0000266	abnormal heart morphology	Slc35b4<tm1.1(KOMP)Vlcg>/Slc35b4<+>	C57BL/6N-Slc35b4<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:5797819	M	MP:0005561	increased mean corpuscular hemoglobin	Slc38a2<tm1a(KOMP)Wtsi>/Slc38a2<+>	C57BL/6N-Slc38a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797819	M	MP:0000559	abnormal femur morphology	Slc38a2<tm1a(KOMP)Wtsi>/Slc38a2<+>	C57BL/6N-Slc38a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797819	M	MP:0005179	decreased circulating cholesterol level	Slc38a2<tm1a(KOMP)Wtsi>/Slc38a2<+>	C57BL/6N-Slc38a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797819	M	MP:0005560	decreased circulating glucose level	Slc38a2<tm1a(KOMP)Wtsi>/Slc38a2<+>	C57BL/6N-Slc38a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797819	M	MP:0000186	decreased circulating HDL cholesterol level	Slc38a2<tm1a(KOMP)Wtsi>/Slc38a2<+>	C57BL/6N-Slc38a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797819	M	MP:0000218	increased leukocyte cell number	Slc38a2<tm1a(KOMP)Wtsi>/Slc38a2<+>	C57BL/6N-Slc38a2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797821	M	MP:0002631	abnormal epididymis morphology	Slc6a14<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Slc6a14<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797821	M	MP:0004931	enlarged epididymis	Slc6a14<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Slc6a14<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797822	M	MP:0005293	impaired glucose tolerance	Slc6a2<tm1b(EUCOMM)Hmgu>/Slc6a2<+>	C57BL/6N-Slc6a2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797822	M	MP:0002874	decreased hemoglobin content	Slc6a2<tm1b(EUCOMM)Hmgu>/Slc6a2<+>	C57BL/6N-Slc6a2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797823	M	MP:0001406	abnormal gait	Slc6a2<tm1b(EUCOMM)Hmgu>/Slc6a2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc6a2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797823	F	MP:0002188	small heart	Slc6a2<tm1b(EUCOMM)Hmgu>/Slc6a2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc6a2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797824	F	MP:0000194	increased circulating calcium level	Slc9a3<tm1b(NCOM)Mfgc>/Slc9a3<+>	C57BL/6N-Slc9a3<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797825	F	MP:0010506	prolonged RR interval	Slfn1<tm1.1(KOMP)Vlcg>/Slfn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slfn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797825	F	MP:0005333	decreased heart rate	Slfn1<tm1.1(KOMP)Vlcg>/Slfn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slfn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797826	M	MP:0009142	decreased prepulse inhibition	Smim8<tm1.1(KOMP)Vlcg>/Smim8<tm1.1(KOMP)Vlcg>	C57BL/6N-Smim8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797826	M	MP:0000274	enlarged heart	Smim8<tm1.1(KOMP)Vlcg>/Smim8<tm1.1(KOMP)Vlcg>	C57BL/6N-Smim8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797826	M	MP:0001566	increased circulating phosphate level	Smim8<tm1.1(KOMP)Vlcg>/Smim8<tm1.1(KOMP)Vlcg>	C57BL/6N-Smim8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797826	M	MP:0000266	abnormal heart morphology	Smim8<tm1.1(KOMP)Vlcg>/Smim8<tm1.1(KOMP)Vlcg>	C57BL/6N-Smim8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797826	M	MP:0002968	increased circulating alkaline phosphatase level	Smim8<tm1.1(KOMP)Vlcg>/Smim8<tm1.1(KOMP)Vlcg>	C57BL/6N-Smim8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797826	M	MP:0011110	preweaning lethality, incomplete penetrance	Smim8<tm1.1(KOMP)Vlcg>/Smim8<tm1.1(KOMP)Vlcg>	C57BL/6N-Smim8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797827	F	MP:0012362	increased large unstained cell number	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<+>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797827	M	MP:0002833	increased heart weight	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<+>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797827	M	MP:0005016	decreased lymphocyte cell number	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<+>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797827	M	MP:0004151	decreased circulating iron level	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<+>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797827	M	MP:0000219	increased neutrophil cell number	Smoc1<tm1b(EUCOMM)Wtsi>/Smoc1<+>	C57BL/6N-Smoc1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797828	M	MP:0005633	increased circulating sodium level	Smoc2<tm1.1(KOMP)Vlcg>/Smoc2<tm1.1(KOMP)Vlcg>	C57BL/6N-Smoc2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797828	M	MP:0001566	increased circulating phosphate level	Smoc2<tm1.1(KOMP)Vlcg>/Smoc2<tm1.1(KOMP)Vlcg>	C57BL/6N-Smoc2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797828	F	MP:0003795	abnormal bone structure	Smoc2<tm1.1(KOMP)Vlcg>/Smoc2<tm1.1(KOMP)Vlcg>	C57BL/6N-Smoc2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797828	F	MP:0000063	decreased bone mineral density	Smoc2<tm1.1(KOMP)Vlcg>/Smoc2<tm1.1(KOMP)Vlcg>	C57BL/6N-Smoc2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797828	F	MP:0010124	decreased bone mineral content	Smoc2<tm1.1(KOMP)Vlcg>/Smoc2<tm1.1(KOMP)Vlcg>	C57BL/6N-Smoc2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797829	M	MP:0001512	trunk curl	Smurf1<tm1b(EUCOMM)Wtsi>/Smurf1<+>	C57BL/6N-Smurf1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797831	M	MP:0000274	enlarged heart	Snai2<tm1.1(KOMP)Vlcg>/Snai2<+>	C57BL/6N-Snai2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797832	M	MP:0010124	decreased bone mineral content	Sncb<tm1b(EUCOMM)Hmgu>/Sncb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sncb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797832	M	MP:0005293	impaired glucose tolerance	Sncb<tm1b(EUCOMM)Hmgu>/Sncb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sncb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797833	M	MP:0002753	dilated heart left ventricle	Snx25<tm1b(KOMP)Wtsi>/Snx25<+>	C57BL/6N-Snx25<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797833	F	MP:0001399	hyperactivity	Snx25<tm1b(KOMP)Wtsi>/Snx25<+>	C57BL/6N-Snx25<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797834	F	MP:0002875	decreased erythrocyte cell number	Snx27<tm1b(KOMP)Wtsi>/Snx27<+>	C57BL/6N-Snx27<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797834	F	MP:0002874	decreased hemoglobin content	Snx27<tm1b(KOMP)Wtsi>/Snx27<+>	C57BL/6N-Snx27<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797834	F	MP:0000208	decreased hematocrit	Snx27<tm1b(KOMP)Wtsi>/Snx27<+>	C57BL/6N-Snx27<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797835	F	MP:0005333	decreased heart rate	Snx29<tm1b(EUCOMM)Hmgu>/Snx29<tm1b(EUCOMM)Hmgu>	C57BL/6N-Snx29<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5797835	M	MP:0011940	decreased food intake	Snx29<tm1b(EUCOMM)Hmgu>/Snx29<tm1b(EUCOMM)Hmgu>	C57BL/6N-Snx29<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5797837	F	MP:0001399	hyperactivity	Spag4<tm1.1(KOMP)Mbp>/Spag4<tm1.1(KOMP)Mbp>	C57BL/6N-Spag4<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5797838	F	MP:0001891	hydrocephaly	Spast<tm1b(KOMP)Wtsi>/Spast<tm1b(KOMP)Wtsi>	C57BL/6N-Spast<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797838	F	MP:0002152	abnormal brain morphology	Spast<tm1b(KOMP)Wtsi>/Spast<tm1b(KOMP)Wtsi>	C57BL/6N-Spast<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5797839	M	MP:0001925	male infertility	Spata22<tm1b(KOMP)Wtsi>/Spata22<tm1b(KOMP)Wtsi>	C57BL/6N-Spata22<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797839	F	MP:0003795	abnormal bone structure	Spata22<tm1b(KOMP)Wtsi>/Spata22<tm1b(KOMP)Wtsi>	C57BL/6N-Spata22<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797839	M	MP:0000274	enlarged heart	Spata22<tm1b(KOMP)Wtsi>/Spata22<tm1b(KOMP)Wtsi>	C57BL/6N-Spata22<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797839	F	MP:0000063	decreased bone mineral density	Spata22<tm1b(KOMP)Wtsi>/Spata22<tm1b(KOMP)Wtsi>	C57BL/6N-Spata22<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797839	M	MP:0004931	enlarged epididymis	Spata22<tm1b(KOMP)Wtsi>/Spata22<tm1b(KOMP)Wtsi>	C57BL/6N-Spata22<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797839	F	MP:0010124	decreased bone mineral content	Spata22<tm1b(KOMP)Wtsi>/Spata22<tm1b(KOMP)Wtsi>	C57BL/6N-Spata22<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797839	M	MP:0001147	small testis	Spata22<tm1b(KOMP)Wtsi>/Spata22<tm1b(KOMP)Wtsi>	C57BL/6N-Spata22<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797839	M	MP:0001146	abnormal testis morphology	Spata22<tm1b(KOMP)Wtsi>/Spata22<tm1b(KOMP)Wtsi>	C57BL/6N-Spata22<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797839	M	MP:0001944	abnormal pancreas morphology	Spata22<tm1b(KOMP)Wtsi>/Spata22<tm1b(KOMP)Wtsi>	C57BL/6N-Spata22<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797839	F	MP:0001926	female infertility	Spata22<tm1b(KOMP)Wtsi>/Spata22<tm1b(KOMP)Wtsi>	C57BL/6N-Spata22<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797839	M	MP:0000266	abnormal heart morphology	Spata22<tm1b(KOMP)Wtsi>/Spata22<tm1b(KOMP)Wtsi>	C57BL/6N-Spata22<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797841	M	MP:0002606	increased basophil cell number	Speg<tm1b(KOMP)Wtsi>/Speg<+>	C57BL/6N-Speg<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:5797842	F	MP:0010574	dilated aorta	Spart<tm2b(EUCOMM)Hmgu>/Spart<tm2b(EUCOMM)Hmgu>	C57BL/6N-Spart<tm2b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5797842	M	MP:0013279	increased fasting circulating glucose level	Spart<tm2b(EUCOMM)Hmgu>/Spart<tm2b(EUCOMM)Hmgu>	C57BL/6N-Spart<tm2b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5797842	M	MP:0001417	decreased exploration in new environment	Spart<tm2b(EUCOMM)Hmgu>/Spart<tm2b(EUCOMM)Hmgu>	C57BL/6N-Spart<tm2b(EUCOMM)Hmgu>/Cnrm	N	MGI:5576271
MGI:5797843	F	MP:0002968	increased circulating alkaline phosphatase level	Spice1<tm1b(EUCOMM)Hmgu>/Spice1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spice1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797843	M	MP:0010067	increased red blood cell distribution width	Spice1<tm1b(EUCOMM)Hmgu>/Spice1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spice1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797844	F	MP:0002606	increased basophil cell number	Spink2<tm1.1(KOMP)Vlcg>/Spink2<tm1.1(KOMP)Vlcg>	C57BL/6N-Spink2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797844	F	MP:0002875	decreased erythrocyte cell number	Spink2<tm1.1(KOMP)Vlcg>/Spink2<tm1.1(KOMP)Vlcg>	C57BL/6N-Spink2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797844	M	MP:0002631	abnormal epididymis morphology	Spink2<tm1.1(KOMP)Vlcg>/Spink2<tm1.1(KOMP)Vlcg>	C57BL/6N-Spink2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797844	M	MP:0001925	male infertility	Spink2<tm1.1(KOMP)Vlcg>/Spink2<tm1.1(KOMP)Vlcg>	C57BL/6N-Spink2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797846	F	MP:0011436	decreased urine magnesium level	Sprr3<tm1.1(KOMP)Vlcg>/Sprr3<tm1.1(KOMP)Vlcg>	C57BL/6N-Sprr3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797847	M	MP:0002833	increased heart weight	Srcin1<tm1.1(KOMP)Vlcg>/Srcin1<+>	C57BL/6N-Srcin1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797847	M	MP:0010123	increased bone mineral content	Srcin1<tm1.1(KOMP)Vlcg>/Srcin1<+>	C57BL/6N-Srcin1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797849	F	MP:0002966	decreased circulating alkaline phosphatase level	Stat1<tm2b(EUCOMM)Wtsi>/Stat1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Stat1<tm2b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:5797849	M	MP:0001406	abnormal gait	Stat1<tm2b(EUCOMM)Wtsi>/Stat1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Stat1<tm2b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:5797849	F	MP:0012362	increased large unstained cell number	Stat1<tm2b(EUCOMM)Wtsi>/Stat1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Stat1<tm2b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:5797849	F	MP:0005011	increased eosinophil cell number	Stat1<tm2b(EUCOMM)Wtsi>/Stat1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Stat1<tm2b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:5797849	M	MP:0001523	impaired righting response	Stat1<tm2b(EUCOMM)Wtsi>/Stat1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Stat1<tm2b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:5797850	F	MP:0010067	increased red blood cell distribution width	Stra6l<tm1b(KOMP)Wtsi>/Stra6l<tm1b(KOMP)Wtsi>	C57BL/6N-Stra6l<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797850	M	MP:0001314	cornea opacity	Stra6l<tm1b(KOMP)Wtsi>/Stra6l<tm1b(KOMP)Wtsi>	C57BL/6N-Stra6l<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797850	F	MP:0005016	decreased lymphocyte cell number	Stra6l<tm1b(KOMP)Wtsi>/Stra6l<tm1b(KOMP)Wtsi>	C57BL/6N-Stra6l<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797850	F	MP:0005561	increased mean corpuscular hemoglobin	Stra6l<tm1b(KOMP)Wtsi>/Stra6l<tm1b(KOMP)Wtsi>	C57BL/6N-Stra6l<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797850	F	MP:0000219	increased neutrophil cell number	Stra6l<tm1b(KOMP)Wtsi>/Stra6l<tm1b(KOMP)Wtsi>	C57BL/6N-Stra6l<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797850	F	MP:0002590	increased mean corpuscular volume	Stra6l<tm1b(KOMP)Wtsi>/Stra6l<tm1b(KOMP)Wtsi>	C57BL/6N-Stra6l<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797850	F	MP:0002606	increased basophil cell number	Stra6l<tm1b(KOMP)Wtsi>/Stra6l<tm1b(KOMP)Wtsi>	C57BL/6N-Stra6l<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797850	F	MP:0002599	increased mean platelet volume	Stra6l<tm1b(KOMP)Wtsi>/Stra6l<tm1b(KOMP)Wtsi>	C57BL/6N-Stra6l<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797851	M	MP:0001488	increased startle reflex	Sufu<tm1b(KOMP)Wtsi>/Sufu<+>	C57BL/6N-Sufu<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797851	M	MP:0000702	enlarged lymph nodes	Sufu<tm1b(KOMP)Wtsi>/Sufu<+>	C57BL/6N-Sufu<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797851	F	MP:0005385	cardiovascular system phenotype	Sufu<tm1b(KOMP)Wtsi>/Sufu<+>	C57BL/6N-Sufu<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797851	F	MP:0010025	decreased total body fat amount	Sufu<tm1b(KOMP)Wtsi>/Sufu<+>	C57BL/6N-Sufu<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797851	M	MP:0000470	abnormal stomach morphology	Sufu<tm1b(KOMP)Wtsi>/Sufu<+>	C57BL/6N-Sufu<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797852	M	MP:0000063	decreased bone mineral density	Tardbp<tm1b(EUCOMM)Wtsi>/Tardbp<+>	C57BL/6N-Tardbp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797852	M	MP:0001486	abnormal startle reflex	Tardbp<tm1b(EUCOMM)Wtsi>/Tardbp<+>	C57BL/6N-Tardbp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797852	M	MP:0010124	decreased bone mineral content	Tardbp<tm1b(EUCOMM)Wtsi>/Tardbp<+>	C57BL/6N-Tardbp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797852	F	MP:0008935	decreased mean platelet volume	Tardbp<tm1b(EUCOMM)Wtsi>/Tardbp<+>	C57BL/6N-Tardbp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797852	F	MP:0005566	decreased blood urea nitrogen level	Tardbp<tm1b(EUCOMM)Wtsi>/Tardbp<+>	C57BL/6N-Tardbp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5797853	M	MP:0000063	decreased bone mineral density	Tatdn3<tm1b(EUCOMM)Wtsi>/Tatdn3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tatdn3<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797853	M	MP:0010024	increased total body fat amount	Tatdn3<tm1b(EUCOMM)Wtsi>/Tatdn3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tatdn3<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797854	F	MP:0003179	thrombocytopenia	Tbc1d22a<tm1b(KOMP)Wtsi>/Tbc1d22a<tm1b(KOMP)Wtsi>	C57BL/6N-Tbc1d22a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797854	M	MP:0002644	decreased circulating triglyceride level	Tbc1d22a<tm1b(KOMP)Wtsi>/Tbc1d22a<tm1b(KOMP)Wtsi>	C57BL/6N-Tbc1d22a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797854	F	MP:0005553	increased circulating creatinine level	Tbc1d22a<tm1b(KOMP)Wtsi>/Tbc1d22a<tm1b(KOMP)Wtsi>	C57BL/6N-Tbc1d22a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797854	F	MP:0001554	increased circulating free fatty acids level	Tbc1d22a<tm1b(KOMP)Wtsi>/Tbc1d22a<tm1b(KOMP)Wtsi>	C57BL/6N-Tbc1d22a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797854	M	MP:0008806	increased circulating amylase level	Tbc1d22a<tm1b(KOMP)Wtsi>/Tbc1d22a<tm1b(KOMP)Wtsi>	C57BL/6N-Tbc1d22a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797854	M	MP:0010067	increased red blood cell distribution width	Tbc1d22a<tm1b(KOMP)Wtsi>/Tbc1d22a<tm1b(KOMP)Wtsi>	C57BL/6N-Tbc1d22a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797855	F	MP:0002608	increased hematocrit	Tbc1d4<tm1b(EUCOMM)Hmgu>/Tbc1d4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tbc1d4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797855	M	MP:0002590	increased mean corpuscular volume	Tbc1d4<tm1b(EUCOMM)Hmgu>/Tbc1d4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tbc1d4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797856	F	MP:0001415	increased exploration in new environment	Tbx22<tm1.1(KOMP)Vlcg>/Tbx22<tm1.1(KOMP)Vlcg>	C57BL/6N-Tbx22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797856	F	MP:0005561	increased mean corpuscular hemoglobin	Tbx22<tm1.1(KOMP)Vlcg>/Tbx22<tm1.1(KOMP)Vlcg>	C57BL/6N-Tbx22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797858	F	MP:0013630	increased bone trabecular spacing	Tead3<tm1a(EUCOMM)Wtsi>/Tead3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tead3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797858	M	MP:0005419	decreased circulating serum albumin level	Tead3<tm1a(EUCOMM)Wtsi>/Tead3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tead3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797858	F	MP:0010869	decreased bone trabecula number	Tead3<tm1a(EUCOMM)Wtsi>/Tead3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tead3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797859	M	MP:0010052	increased grip strength	Tep1<tm1b(NCOM)Mfgc>/Tep1<tm1b(NCOM)Mfgc>	C57BL/6N-Tep1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797860	F	MP:0001513	limb grasping	Tex29<tm1.1(KOMP)Vlcg>/Tex29<tm1.1(KOMP)Vlcg>	C57BL/6N-Tex29<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797861	F	MP:0000266	abnormal heart morphology	Tfap4<tm1.1(KOMP)Vlcg>/Tfap4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tfap4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797861	M	MP:0003960	increased lean body mass	Tfap4<tm1.1(KOMP)Vlcg>/Tfap4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tfap4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797861	F	MP:0001120	abnormal uterus morphology	Tfap4<tm1.1(KOMP)Vlcg>/Tfap4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tfap4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797861	M	MP:0004956	decreased thymus weight	Tfap4<tm1.1(KOMP)Vlcg>/Tfap4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tfap4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797861	M	MP:0003402	decreased liver weight	Tfap4<tm1.1(KOMP)Vlcg>/Tfap4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tfap4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797861	F	MP:0005333	decreased heart rate	Tfap4<tm1.1(KOMP)Vlcg>/Tfap4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tfap4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797861	M	MP:0011110	preweaning lethality, incomplete penetrance	Tfap4<tm1.1(KOMP)Vlcg>/Tfap4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tfap4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797861	F	MP:0010506	prolonged RR interval	Tfap4<tm1.1(KOMP)Vlcg>/Tfap4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tfap4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797862	M	MP:0000702	enlarged lymph nodes	Tgfb3<tm1.1(KOMP)Vlcg>/Tgfb3<+>	C57BL/6N-Tgfb3<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797862	M	MP:0001146	abnormal testis morphology	Tgfb3<tm1.1(KOMP)Vlcg>/Tgfb3<+>	C57BL/6N-Tgfb3<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797863	F	MP:0002941	increased circulating alanine transaminase level	Thbs1<tm1.1(KOMP)Vlcg>/Thbs1<tm1.1(KOMP)Vlcg>	C57BL/6N-Thbs1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797863	M	MP:0001175	abnormal lung morphology	Thbs1<tm1.1(KOMP)Vlcg>/Thbs1<tm1.1(KOMP)Vlcg>	C57BL/6N-Thbs1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797863	M	MP:0000598	abnormal liver morphology	Thbs1<tm1.1(KOMP)Vlcg>/Thbs1<tm1.1(KOMP)Vlcg>	C57BL/6N-Thbs1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797863	M	MP:0000266	abnormal heart morphology	Thbs1<tm1.1(KOMP)Vlcg>/Thbs1<tm1.1(KOMP)Vlcg>	C57BL/6N-Thbs1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797863	F	MP:0010123	increased bone mineral content	Thbs1<tm1.1(KOMP)Vlcg>/Thbs1<tm1.1(KOMP)Vlcg>	C57BL/6N-Thbs1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797864	M	MP:0001314	cornea opacity	Thpo<tm1.1(KOMP)Vlcg>/Thpo<tm1.1(KOMP)Vlcg>	C57BL/6N-Thpo<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797864	F	MP:0002599	increased mean platelet volume	Thpo<tm1.1(KOMP)Vlcg>/Thpo<tm1.1(KOMP)Vlcg>	C57BL/6N-Thpo<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797864	F	MP:0000438	abnormal cranium morphology	Thpo<tm1.1(KOMP)Vlcg>/Thpo<tm1.1(KOMP)Vlcg>	C57BL/6N-Thpo<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797865	M	MP:0001510	abnormal coat appearance	Timmdc1<tm1b(EUCOMM)Wtsi>/Timmdc1<+>	C57BL/6N-Timmdc1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797865	M	MP:0002941	increased circulating alanine transaminase level	Timmdc1<tm1b(EUCOMM)Wtsi>/Timmdc1<+>	C57BL/6N-Timmdc1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797866	M	MP:0001147	small testis	Tmed10<tm1.1(KOMP)Vlcg>/Tmed10<+>	C57BL/6N-Tmed10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797866	M	MP:0001146	abnormal testis morphology	Tmed10<tm1.1(KOMP)Vlcg>/Tmed10<+>	C57BL/6N-Tmed10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797866	M	MP:0001891	hydrocephaly	Tmed10<tm1.1(KOMP)Vlcg>/Tmed10<+>	C57BL/6N-Tmed10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797866	M	MP:0002135	abnormal kidney morphology	Tmed10<tm1.1(KOMP)Vlcg>/Tmed10<+>	C57BL/6N-Tmed10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797869	F	MP:0002833	increased heart weight	Tmem181a<tm1b(EUCOMM)Wtsi>/Tmem181a<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem181a<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:5797871	F	MP:0003271	abnormal duodenum morphology	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0000703	abnormal thymus morphology	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0002135	abnormal kidney morphology	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0003402	decreased liver weight	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0004956	decreased thymus weight	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	F	MP:0000495	abnormal colon morphology	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0000208	decreased hematocrit	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0005179	decreased circulating cholesterol level	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0000689	abnormal spleen morphology	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	F	MP:0000642	enlarged adrenal glands	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0010025	decreased total body fat amount	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0002175	decreased brain weight	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	F	MP:0001926	female infertility	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0000706	small thymus	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	F	MP:0004002	abnormal jejunum morphology	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0002875	decreased erythrocyte cell number	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0002968	increased circulating alkaline phosphatase level	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0001157	small seminal vesicle	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797871	M	MP:0002059	abnormal seminal vesicle morphology	Tmem248<tm1.1(KOMP)Vlcg>/Tmem248<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797872	M	MP:0000195	decreased circulating calcium level	Tmem254<tm2a(KOMP)Wtsi>/Tmem254<tm2a(KOMP)Wtsi>	C57BL/6N-Tmem254<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797873	M	MP:0000186	decreased circulating HDL cholesterol level	Tmem42<tm1b(KOMP)Wtsi>/Tmem42<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem42<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797873	M	MP:0003960	increased lean body mass	Tmem42<tm1b(KOMP)Wtsi>/Tmem42<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem42<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797873	M	MP:0010123	increased bone mineral content	Tmem42<tm1b(KOMP)Wtsi>/Tmem42<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem42<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797873	M	MP:0000062	increased bone mineral density	Tmem42<tm1b(KOMP)Wtsi>/Tmem42<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem42<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797874	F	MP:0001325	abnormal retina morphology	Tmem79<tm1.1(KOMP)Wtsi>/Tmem79<tm1.1(KOMP)Wtsi>	C57BL/6N-Tmem79<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797874	M	MP:0005561	increased mean corpuscular hemoglobin	Tmem79<tm1.1(KOMP)Wtsi>/Tmem79<tm1.1(KOMP)Wtsi>	C57BL/6N-Tmem79<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797874	M	MP:0002833	increased heart weight	Tmem79<tm1.1(KOMP)Wtsi>/Tmem79<tm1.1(KOMP)Wtsi>	C57BL/6N-Tmem79<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797875	M	MP:0001489	decreased startle reflex	Tmtc4<tm1.1(KOMP)Vlcg>/Tmtc4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmtc4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797876	F	MP:0010506	prolonged RR interval	Tnfrsf17<tm1.1(KOMP)Vlcg>/Tnfrsf17<tm1.1(KOMP)Vlcg>	C57BL/6N-Tnfrsf17<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797876	F	MP:0005333	decreased heart rate	Tnfrsf17<tm1.1(KOMP)Vlcg>/Tnfrsf17<tm1.1(KOMP)Vlcg>	C57BL/6N-Tnfrsf17<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5797877	F	MP:0002092	abnormal eye morphology	Tnfrsf18<tm1.1(KOMP)Vlcg>/Tnfrsf18<tm1.1(KOMP)Vlcg>	C57BL/6N-Tnfrsf18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797879	F	MP:0002941	increased circulating alanine transaminase level	Tnfsf10<tm1b(KOMP)Wtsi>/Tnfsf10<tm1b(KOMP)Wtsi>	C57BL/6N-Tnfsf10<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797880	M	MP:0002608	increased hematocrit	Tnfsf18<tm1.1(KOMP)Vlcg>/Tnfsf18<tm1.1(KOMP)Vlcg>	C57BL/6N-Tnfsf18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797880	M	MP:0003961	decreased lean body mass	Tnfsf18<tm1.1(KOMP)Vlcg>/Tnfsf18<tm1.1(KOMP)Vlcg>	C57BL/6N-Tnfsf18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797881	M	MP:0010124	decreased bone mineral content	Tnxb<tm1b(EUCOMM)Hmgu>/Tnxb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnxb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797881	M	MP:0000691	enlarged spleen	Tnxb<tm1b(EUCOMM)Hmgu>/Tnxb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnxb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797881	M	MP:0000274	enlarged heart	Tnxb<tm1b(EUCOMM)Hmgu>/Tnxb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnxb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797882	M	MP:0005011	increased eosinophil cell number	Tpcn2<tm1b(EUCOMM)Hmgu>/Tpcn2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tpcn2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797882	M	MP:0001552	increased circulating triglyceride level	Tpcn2<tm1b(EUCOMM)Hmgu>/Tpcn2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tpcn2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797883	F	MP:0003961	decreased lean body mass	Trappc10<tm1b(KOMP)Wtsi>/Trappc10<tm1b(KOMP)Wtsi>	C57BL/6N-Trappc10<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797883	F	MP:0005178	increased circulating cholesterol level	Trappc10<tm1b(KOMP)Wtsi>/Trappc10<tm1b(KOMP)Wtsi>	C57BL/6N-Trappc10<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797883	M	MP:0005562	decreased mean corpuscular hemoglobin	Trappc10<tm1b(KOMP)Wtsi>/Trappc10<tm1b(KOMP)Wtsi>	C57BL/6N-Trappc10<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797883	F	MP:0010024	increased total body fat amount	Trappc10<tm1b(KOMP)Wtsi>/Trappc10<tm1b(KOMP)Wtsi>	C57BL/6N-Trappc10<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797883	F	MP:0010124	decreased bone mineral content	Trappc10<tm1b(KOMP)Wtsi>/Trappc10<tm1b(KOMP)Wtsi>	C57BL/6N-Trappc10<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797883	M	MP:0002079	increased circulating insulin level	Trappc10<tm1b(KOMP)Wtsi>/Trappc10<tm1b(KOMP)Wtsi>	C57BL/6N-Trappc10<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797884	M	MP:0001258	decreased body length	Trappc2<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Trappc2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797885	F	MP:0009709	hydrometra	Trappc2<tm1.1(KOMP)Vlcg>/Trappc2<tm1.1(KOMP)Vlcg>	C57BL/6N-Trappc2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797886	F	MP:0003961	decreased lean body mass	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trappc9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797886	F	MP:0010067	increased red blood cell distribution width	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trappc9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797886	F	MP:0010124	decreased bone mineral content	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trappc9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797886	F	MP:0002079	increased circulating insulin level	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trappc9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797886	F	MP:0010024	increased total body fat amount	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trappc9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797886	F	MP:0000220	increased monocyte cell number	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trappc9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797886	M	MP:0002098	abnormal vibrissa morphology	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trappc9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797886	F	MP:0005293	impaired glucose tolerance	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trappc9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797886	M	MP:0005562	decreased mean corpuscular hemoglobin	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trappc9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797886	F	MP:0013025	increased Ly6C low monocyte number	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trappc9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797886	F	MP:0013022	increased Ly6C high monocyte number	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trappc9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797886	F	MP:0008347	decreased gamma-delta T cell number	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trappc9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797886	M	MP:0005633	increased circulating sodium level	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trappc9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797888	F	MP:0010052	increased grip strength	Trim56<tm1a(EUCOMM)Wtsi>/Trim56<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trim56<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797888	M	MP:0004974	decreased regulatory T cell number	Trim56<tm1a(EUCOMM)Wtsi>/Trim56<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trim56<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797888	M	MP:0005179	decreased circulating cholesterol level	Trim56<tm1a(EUCOMM)Wtsi>/Trim56<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trim56<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797888	M	MP:0000186	decreased circulating HDL cholesterol level	Trim56<tm1a(EUCOMM)Wtsi>/Trim56<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trim56<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797888	M	MP:0004151	decreased circulating iron level	Trim56<tm1a(EUCOMM)Wtsi>/Trim56<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trim56<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797888	F	MP:0008810	increased circulating iron level	Trim56<tm1a(EUCOMM)Wtsi>/Trim56<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trim56<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797891	M	MP:0001402	decreased locomotor activity	Tsg101<tm1b(EUCOMM)Hmgu>/Tsg101<+>	C57BL/6N-Tsg101<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5797891	F	MP:0002135	abnormal kidney morphology	Tsg101<tm1b(EUCOMM)Hmgu>/Tsg101<+>	C57BL/6N-Tsg101<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:5797893	F	MP:0000221	decreased leukocyte cell number	Tssk5<tm1.1(KOMP)Vlcg>/Tssk5<tm1.1(KOMP)Vlcg>	C57BL/6N-Tssk5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797894	M	MP:0005627	increased circulating potassium level	Ttll6<tm1.1(KOMP)Vlcg>/Ttll6<tm1.1(KOMP)Vlcg>	C57BL/6N-Ttll6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797895	M	MP:0001146	abnormal testis morphology	Twist2<tm1.1(KOMP)Vlcg>/Twist2<+>	C57BL/6N-Twist2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797895	M	MP:0000274	enlarged heart	Twist2<tm1.1(KOMP)Vlcg>/Twist2<+>	C57BL/6N-Twist2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797895	M	MP:0000266	abnormal heart morphology	Twist2<tm1.1(KOMP)Vlcg>/Twist2<+>	C57BL/6N-Twist2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797895	M	MP:0001147	small testis	Twist2<tm1.1(KOMP)Vlcg>/Twist2<+>	C57BL/6N-Twist2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797895	M	MP:0001175	abnormal lung morphology	Twist2<tm1.1(KOMP)Vlcg>/Twist2<+>	C57BL/6N-Twist2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797895	M	MP:0004882	enlarged lung	Twist2<tm1.1(KOMP)Vlcg>/Twist2<+>	C57BL/6N-Twist2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797896	M	MP:0002644	decreased circulating triglyceride level	Ubash3a<tm1b(KOMP)Wtsi>/Ubash3a<tm1b(KOMP)Wtsi>	C57BL/6N-Ubash3a<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5797896	M	MP:0001304	cataract	Ubash3a<tm1b(KOMP)Wtsi>/Ubash3a<tm1b(KOMP)Wtsi>	C57BL/6N-Ubash3a<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:5797897	F	MP:0005633	increased circulating sodium level	Ube2m<tm1.1(KOMP)Wtsi>/Ube2m<+>	C57BL/6N-Ube2m<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797898	F	MP:0011100	preweaning lethality, complete penetrance	Ubr2<tm1e.1(KOMP)Mbp>/Ubr2<tm1e.1(KOMP)Mbp>	C57BL/6N-Ubr2<tm1e.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:5797899	M	MP:0001488	increased startle reflex	Uchl1<tm1b(EUCOMM)Hmgu>/Uchl1<+>	C57BL/6N-Uchl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797899	F	MP:0002968	increased circulating alkaline phosphatase level	Uchl1<tm1b(EUCOMM)Hmgu>/Uchl1<+>	C57BL/6N-Uchl1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5797900	F	MP:0005553	increased circulating creatinine level	Ucn3<tm1.1(KOMP)Vlcg>/Ucn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ucn3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797900	F	MP:0000274	enlarged heart	Ucn3<tm1.1(KOMP)Vlcg>/Ucn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ucn3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797900	F	MP:0000266	abnormal heart morphology	Ucn3<tm1.1(KOMP)Vlcg>/Ucn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ucn3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797901	M	MP:0000274	enlarged heart	Unc119<tm1.1(KOMP)Vlcg>/Unc119<+>	C57BL/6N-Unc119<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797903	F	MP:0002968	increased circulating alkaline phosphatase level	Usp20<tm1a(EUCOMM)Hmgu>/Usp20<tm1a(EUCOMM)Hmgu>	C57BL/6N-Usp20<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:5797905	M	MP:0009142	decreased prepulse inhibition	Usp50<tm1(KOMP)Vlcg>/Usp50<+>	C57BL/6N-Usp50<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5797905	M	MP:0001319	irregularly shaped pupil	Usp50<tm1(KOMP)Vlcg>/Usp50<+>	C57BL/6N-Usp50<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:5797906	M	MP:0002098	abnormal vibrissa morphology	Vamp3<tm2b(EUCOMM)Wtsi>/Vamp3<tm2b(EUCOMM)Wtsi>	C57BL/6N-Vamp3<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797907	M	MP:0005344	increased circulating bilirubin level	Vcpkmt<tm1.1(KOMP)Vlcg>/Vcpkmt<tm1.1(KOMP)Vlcg>	C57BL/6N-Vcpkmt<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797907	F	MP:0005278	abnormal cholesterol homeostasis	Vcpkmt<tm1.1(KOMP)Vlcg>/Vcpkmt<tm1.1(KOMP)Vlcg>	C57BL/6N-Vcpkmt<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797907	F	MP:0002833	increased heart weight	Vcpkmt<tm1.1(KOMP)Vlcg>/Vcpkmt<tm1.1(KOMP)Vlcg>	C57BL/6N-Vcpkmt<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797908	M	MP:0002968	increased circulating alkaline phosphatase level	Vps13c<tm1b(EUCOMM)Hmgu>/Vps13c<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vps13c<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:5797909	F	MP:0005560	decreased circulating glucose level	Vsig4<tm1b(EUCOMM)Hmgu>/Vsig4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797909	F	MP:0005633	increased circulating sodium level	Vsig4<tm1b(EUCOMM)Hmgu>/Vsig4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797909	F	MP:0002959	increased urine microalbumin level	Vsig4<tm1b(EUCOMM)Hmgu>/Vsig4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797909	F	MP:0002833	increased heart weight	Vsig4<tm1b(EUCOMM)Hmgu>/Vsig4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797909	F	MP:0002574	increased vertical activity	Vsig4<tm1b(EUCOMM)Hmgu>/Vsig4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797909	F	MP:0011396	abnormal sleep behavior	Vsig4<tm1b(EUCOMM)Hmgu>/Vsig4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797909	F	MP:0010025	decreased total body fat amount	Vsig4<tm1b(EUCOMM)Hmgu>/Vsig4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797909	F	MP:0005565	increased blood urea nitrogen level	Vsig4<tm1b(EUCOMM)Hmgu>/Vsig4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797909	F	MP:0001399	hyperactivity	Vsig4<tm1b(EUCOMM)Hmgu>/Vsig4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797909	F	MP:0003960	increased lean body mass	Vsig4<tm1b(EUCOMM)Hmgu>/Vsig4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:5797910	F	MP:0005560	decreased circulating glucose level	Wdr36<tm1.1(KOMP)Vlcg>/Wdr36<+>	C57BL/6N-Wdr36<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797910	F	MP:0004151	decreased circulating iron level	Wdr36<tm1.1(KOMP)Vlcg>/Wdr36<+>	C57BL/6N-Wdr36<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797910	F	MP:0001399	hyperactivity	Wdr36<tm1.1(KOMP)Vlcg>/Wdr36<+>	C57BL/6N-Wdr36<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797910	F	MP:0013279	increased fasting circulating glucose level	Wdr36<tm1.1(KOMP)Vlcg>/Wdr36<+>	C57BL/6N-Wdr36<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5797911	M	MP:0002941	increased circulating alanine transaminase level	Wee1<tm1b(EUCOMM)Wtsi>/Wee1<+>	C57BL/6N-Wee1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:5797912	M	MP:0001510	abnormal coat appearance	Wfdc18<tm1a(KOMP)Wtsi>/Wfdc18<tm1a(KOMP)Wtsi>	C57BL/6N-Wfdc18<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797913	M	MP:0002092	abnormal eye morphology	Wfdc1<tm1.1(KOMP)Vlcg>/Wfdc1<tm1.1(KOMP)Vlcg>	C57BL/6N-Wfdc1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5797914	M	MP:0002152	abnormal brain morphology	Wnt10b<tm1e.1(KOMP)Wtsi>/Wnt10b<tm1e.1(KOMP)Wtsi>	C57BL/6N-Wnt10b<tm1e.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797914	M	MP:0001891	hydrocephaly	Wnt10b<tm1e.1(KOMP)Wtsi>/Wnt10b<tm1e.1(KOMP)Wtsi>	C57BL/6N-Wnt10b<tm1e.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5797915	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Wnt6<tm1b(NCOM)Mfgc>/Wnt6<+>	C57BL/6N-Wnt6<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797917	M	MP:0010088	decreased circulating fructosamine level	Wrap53<tm1b(EUCOMM)Wtsi>/Wrap53<+>	C57BL/6N-Wrap53<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797917	M	MP:0000183	decreased circulating LDL cholesterol level	Wrap53<tm1b(EUCOMM)Wtsi>/Wrap53<+>	C57BL/6N-Wrap53<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797917	M	MP:0000186	decreased circulating HDL cholesterol level	Wrap53<tm1b(EUCOMM)Wtsi>/Wrap53<+>	C57BL/6N-Wrap53<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797917	M	MP:0005179	decreased circulating cholesterol level	Wrap53<tm1b(EUCOMM)Wtsi>/Wrap53<+>	C57BL/6N-Wrap53<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797917	M	MP:0002833	increased heart weight	Wrap53<tm1b(EUCOMM)Wtsi>/Wrap53<+>	C57BL/6N-Wrap53<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797917	M	MP:0003960	increased lean body mass	Wrap53<tm1b(EUCOMM)Wtsi>/Wrap53<+>	C57BL/6N-Wrap53<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797919	M	MP:0002590	increased mean corpuscular volume	Xbp1<tm1b(EUCOMM)Wtsi>/Xbp1<+>	C57BL/6N-Xbp1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797919	M	MP:0005561	increased mean corpuscular hemoglobin	Xbp1<tm1b(EUCOMM)Wtsi>/Xbp1<+>	C57BL/6N-Xbp1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797919	F	MP:0012361	decreased large unstained cell number	Xbp1<tm1b(EUCOMM)Wtsi>/Xbp1<+>	C57BL/6N-Xbp1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797919	F	MP:0010068	decreased red blood cell distribution width	Xbp1<tm1b(EUCOMM)Wtsi>/Xbp1<+>	C57BL/6N-Xbp1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797919	F	MP:0000221	decreased leukocyte cell number	Xbp1<tm1b(EUCOMM)Wtsi>/Xbp1<+>	C57BL/6N-Xbp1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797919	F	MP:0005016	decreased lymphocyte cell number	Xbp1<tm1b(EUCOMM)Wtsi>/Xbp1<+>	C57BL/6N-Xbp1<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:5797921	F	MP:0004794	increased anti-nuclear antigen antibody level	Xkrx<tm1b(EUCOMM)Wtsi>/Xkrx<tm1b(EUCOMM)Wtsi>	C57BL/6N-Xkrx<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797922	M	MP:0004931	enlarged epididymis	Xk<tm1b(KOMP)Mbp>/Y	C57BL/6N-Xk<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5797922	M	MP:0002631	abnormal epididymis morphology	Xk<tm1b(KOMP)Mbp>/Y	C57BL/6N-Xk<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5797923	F	MP:0002060	abnormal skin morphology	Xk<tm1b(KOMP)Mbp>/Xk<tm1b(KOMP)Mbp>	C57BL/6N-Xk<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5797923	F	MP:0002941	increased circulating alanine transaminase level	Xk<tm1b(KOMP)Mbp>/Xk<tm1b(KOMP)Mbp>	C57BL/6N-Xk<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5797923	F	MP:0005343	increased circulating aspartate transaminase level	Xk<tm1b(KOMP)Mbp>/Xk<tm1b(KOMP)Mbp>	C57BL/6N-Xk<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:5797926	M	MP:0000947	convulsive seizures	Zfp14<tm1b(KOMP)Wtsi>/Zfp14<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp14<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797926	M	MP:0002833	increased heart weight	Zfp14<tm1b(KOMP)Wtsi>/Zfp14<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp14<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5797927	M	MP:0001175	abnormal lung morphology	Zfp275<tm1.1(NCOM)Mfgc>/Y	C57BL/6N-Zfp275<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797927	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Zfp275<tm1.1(NCOM)Mfgc>/Y	C57BL/6N-Zfp275<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:5797930	M	MP:0005178	increased circulating cholesterol level	Zfp175<tm1b(EUCOMM)Wtsi>/Zfp175<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp175<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797930	M	MP:0001556	increased circulating HDL cholesterol level	Zfp175<tm1b(EUCOMM)Wtsi>/Zfp175<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp175<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5797931	M	MP:0005505	thrombocytosis	Zranb1<tm1a(EUCOMM)Hmgu>/Zranb1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Zranb1<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5797931	M	MP:0003960	increased lean body mass	Zranb1<tm1a(EUCOMM)Hmgu>/Zranb1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Zranb1<tm1a(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:5797932	F	MP:0005562	decreased mean corpuscular hemoglobin	Zswim1<tm1b(KOMP)Mbp>/Zswim1<tm1b(KOMP)Mbp>	C57BL/6N-Zswim1<tm1b(KOMP)Mbp>/Nju	N	MGI:5576271
MGI:5797932	F	MP:0005013	increased lymphocyte cell number	Zswim1<tm1b(KOMP)Mbp>/Zswim1<tm1b(KOMP)Mbp>	C57BL/6N-Zswim1<tm1b(KOMP)Mbp>/Nju	N	MGI:5576271
MGI:5797932	M	MP:0003960	increased lean body mass	Zswim1<tm1b(KOMP)Mbp>/Zswim1<tm1b(KOMP)Mbp>	C57BL/6N-Zswim1<tm1b(KOMP)Mbp>/Nju	N	MGI:5576271
MGI:5797932	M	MP:0000208	decreased hematocrit	Zswim1<tm1b(KOMP)Mbp>/Zswim1<tm1b(KOMP)Mbp>	C57BL/6N-Zswim1<tm1b(KOMP)Mbp>/Nju	N	MGI:5576271
MGI:5797932	M	MP:0010067	increased red blood cell distribution width	Zswim1<tm1b(KOMP)Mbp>/Zswim1<tm1b(KOMP)Mbp>	C57BL/6N-Zswim1<tm1b(KOMP)Mbp>/Nju	N	MGI:5576271
MGI:5797932	M	MP:0005016	decreased lymphocyte cell number	Zswim1<tm1b(KOMP)Mbp>/Zswim1<tm1b(KOMP)Mbp>	C57BL/6N-Zswim1<tm1b(KOMP)Mbp>/Nju	N	MGI:5576271
MGI:5797932	M	MP:0000219	increased neutrophil cell number	Zswim1<tm1b(KOMP)Mbp>/Zswim1<tm1b(KOMP)Mbp>	C57BL/6N-Zswim1<tm1b(KOMP)Mbp>/Nju	N	MGI:5576271
MGI:5797932	M	MP:0000223	decreased monocyte cell number	Zswim1<tm1b(KOMP)Mbp>/Zswim1<tm1b(KOMP)Mbp>	C57BL/6N-Zswim1<tm1b(KOMP)Mbp>/Nju	N	MGI:5576271
MGI:5797932	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Zswim1<tm1b(KOMP)Mbp>/Zswim1<tm1b(KOMP)Mbp>	C57BL/6N-Zswim1<tm1b(KOMP)Mbp>/Nju	N	MGI:5576271
MGI:5797932	F	MP:0003131	increased erythrocyte cell number	Zswim1<tm1b(KOMP)Mbp>/Zswim1<tm1b(KOMP)Mbp>	C57BL/6N-Zswim1<tm1b(KOMP)Mbp>/Nju	N	MGI:5576271
MGI:5797932	F	MP:0000220	increased monocyte cell number	Zswim1<tm1b(KOMP)Mbp>/Zswim1<tm1b(KOMP)Mbp>	C57BL/6N-Zswim1<tm1b(KOMP)Mbp>/Nju	N	MGI:5576271
MGI:5800315	F	MP:0002869	increased anti-insulin autoantibody level	Irak3<tm1Flv>/Irak3<tm1Flv>	NOD.129S1(B6)-Irak3<tm1Flv>	N	24696448
MGI:5800315	F	MP:0013772	increased effector memory T-helper cell number	Irak3<tm1Flv>/Irak3<tm1Flv>	NOD.129S1(B6)-Irak3<tm1Flv>	N	24696448
MGI:5800315	F	MP:0002145	abnormal T cell differentiation	Irak3<tm1Flv>/Irak3<tm1Flv>	NOD.129S1(B6)-Irak3<tm1Flv>	N	24696448
MGI:5800315	F	MP:0004031	insulitis	Irak3<tm1Flv>/Irak3<tm1Flv>	NOD.129S1(B6)-Irak3<tm1Flv>	N	24696448
MGI:5800315	F	MP:0004803	increased susceptibility to autoimmune diabetes	Irak3<tm1Flv>/Irak3<tm1Flv>	NOD.129S1(B6)-Irak3<tm1Flv>	N	24696448
MGI:5800315	F	MP:0002452	abnormal professional antigen presenting cell physiology	Irak3<tm1Flv>/Irak3<tm1Flv>	NOD.129S1(B6)-Irak3<tm1Flv>	N	24696448
MGI:5800315	F	MP:0002376	abnormal dendritic cell physiology	Irak3<tm1Flv>/Irak3<tm1Flv>	NOD.129S1(B6)-Irak3<tm1Flv>	N	24696448
MGI:5800315	F	MP:0005293	impaired glucose tolerance	Irak3<tm1Flv>/Irak3<tm1Flv>	NOD.129S1(B6)-Irak3<tm1Flv>	N	24696448
MGI:5800315	F	MP:0001828	abnormal T cell activation	Irak3<tm1Flv>/Irak3<tm1Flv>	NOD.129S1(B6)-Irak3<tm1Flv>	N	24696448
MGI:5800331	M	MP:0020254	decreased collagen level	Prxl2a<tm1(KOMP)Vlcg>/Prxl2a<tm1(KOMP)Vlcg>	C57BL/6N-Prxl2a<tm1(KOMP)Vlcg>	N	26629401
MGI:5800331	M	MP:0006319	abnormal epididymal fat pad morphology	Prxl2a<tm1(KOMP)Vlcg>/Prxl2a<tm1(KOMP)Vlcg>	C57BL/6N-Prxl2a<tm1(KOMP)Vlcg>	N	26629401
MGI:5800331	M	MP:0030968	decreased circulating adiponectin level	Prxl2a<tm1(KOMP)Vlcg>/Prxl2a<tm1(KOMP)Vlcg>	C57BL/6N-Prxl2a<tm1(KOMP)Vlcg>	N	26629401
MGI:5800331	M	MP:0004892	increased adiponectin level	Prxl2a<tm1(KOMP)Vlcg>/Prxl2a<tm1(KOMP)Vlcg>	C57BL/6N-Prxl2a<tm1(KOMP)Vlcg>	N	26629401
MGI:5800331	M	MP:0031602	white adipose tissue inflammation	Prxl2a<tm1(KOMP)Vlcg>/Prxl2a<tm1(KOMP)Vlcg>	C57BL/6N-Prxl2a<tm1(KOMP)Vlcg>	N	26629401
MGI:5800331	M	MP:0002079	increased circulating insulin level	Prxl2a<tm1(KOMP)Vlcg>/Prxl2a<tm1(KOMP)Vlcg>	C57BL/6N-Prxl2a<tm1(KOMP)Vlcg>	N	26629401
MGI:5800331	M	MP:0020354	increased endoplasmic reticulum stress	Prxl2a<tm1(KOMP)Vlcg>/Prxl2a<tm1(KOMP)Vlcg>	C57BL/6N-Prxl2a<tm1(KOMP)Vlcg>	N	26629401
MGI:5800331	M	MP:0005378	growth/size/body region phenotype	Prxl2a<tm1(KOMP)Vlcg>/Prxl2a<tm1(KOMP)Vlcg>	C57BL/6N-Prxl2a<tm1(KOMP)Vlcg>	Y	26629401
MGI:5800476	M	MP:0006362	abnormal male germ cell morphology	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800476	M	MP:0008280	abnormal male germ cell apoptosis	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800476	M	MP:0001147	small testis	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800476	M	MP:0002216	abnormal seminiferous tubule morphology	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800476	M	MP:0001153	small seminiferous tubules	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800476	M	MP:0002687	oligozoospermia	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800476	M	MP:0008261	arrest of male meiosis	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800476	M	MP:0001925	male infertility	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800476	M	MP:0010948	abnormal double-strand DNA break repair	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800476	M	MP:0002686	globozoospermia	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800476	M	MP:0004852	decreased testis weight	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800476	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800476	M	MP:0005169	abnormal male meiosis	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800476	M	MP:0001154	seminiferous tubule degeneration	M1ap<Gt(RRO290)Byg>/M1ap<Gt(RRO290)Byg>	involves: 129P2/OlaHsd * C57BL/6	N	23269666
MGI:5800487	M	MP:0001577	anemia	Kcne2<tm1a(EUCOMM)Wtsi>/Kcne2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kcne2<tm1a(EUCOMM)Wtsi>	N	25127743
MGI:5800487	M	MP:0010383	increased adenoma incidence	Kcne2<tm1a(EUCOMM)Wtsi>/Kcne2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kcne2<tm1a(EUCOMM)Wtsi>	N	25127743
MGI:5800487	M	MP:0010067	increased red blood cell distribution width	Kcne2<tm1a(EUCOMM)Wtsi>/Kcne2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kcne2<tm1a(EUCOMM)Wtsi>	N	25127743
MGI:5800487	M	MP:0002874	decreased hemoglobin content	Kcne2<tm1a(EUCOMM)Wtsi>/Kcne2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kcne2<tm1a(EUCOMM)Wtsi>	N	25127743
MGI:5800487	M	MP:0005562	decreased mean corpuscular hemoglobin	Kcne2<tm1a(EUCOMM)Wtsi>/Kcne2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kcne2<tm1a(EUCOMM)Wtsi>	N	25127743
MGI:5800487	M	MP:0000208	decreased hematocrit	Kcne2<tm1a(EUCOMM)Wtsi>/Kcne2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kcne2<tm1a(EUCOMM)Wtsi>	N	25127743
MGI:5800487	M	MP:0011285	increased circulating erythropoietin level	Kcne2<tm1a(EUCOMM)Wtsi>/Kcne2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kcne2<tm1a(EUCOMM)Wtsi>	N	25127743
MGI:5800487	M	MP:0002875	decreased erythrocyte cell number	Kcne2<tm1a(EUCOMM)Wtsi>/Kcne2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kcne2<tm1a(EUCOMM)Wtsi>	N	25127743
MGI:5800487	M	MP:0008388	hypochromic microcytic anemia	Kcne2<tm1a(EUCOMM)Wtsi>/Kcne2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kcne2<tm1a(EUCOMM)Wtsi>	N	25127743
MGI:5800487	M	MP:0002591	decreased mean corpuscular volume	Kcne2<tm1a(EUCOMM)Wtsi>/Kcne2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kcne2<tm1a(EUCOMM)Wtsi>	N	25127743
MGI:5800487	M	MP:0005505	thrombocytosis	Kcne2<tm1a(EUCOMM)Wtsi>/Kcne2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kcne2<tm1a(EUCOMM)Wtsi>	N	25127743
MGI:5800487	F	MP:0005397	hematopoietic system phenotype	Kcne2<tm1a(EUCOMM)Wtsi>/Kcne2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Kcne2<tm1a(EUCOMM)Wtsi>	Y	25127743
MGI:5800537	M	MP:0030949	abnormal Golgi vesicle transport	Plp2<tm1Dva>/Y	involves: 129 * C57BL/6J	N	26512060
MGI:5800537	M	MP:0003076	increased susceptibility to ischemic brain injury	Plp2<tm1Dva>/Y	involves: 129 * C57BL/6J	N	26512060
MGI:5800537	M	MP:0020354	increased endoplasmic reticulum stress	Plp2<tm1Dva>/Y	involves: 129 * C57BL/6J	N	26512060
MGI:5800537	M	MP:0003203	increased neuron apoptosis	Plp2<tm1Dva>/Y	involves: 129 * C57BL/6J	N	26512060
MGI:5800537	M	MP:0013501	increased fibroblast apoptosis	Plp2<tm1Dva>/Y	involves: 129 * C57BL/6J	N	26512060
MGI:5800537	M	MP:0009378	abnormal endoplasmic reticulum morphology	Plp2<tm1Dva>/Y	involves: 129 * C57BL/6J	N	26512060
MGI:5800675	F	MP:0001127	small ovary	Asah1<tm1Medin>/Asah1<tm1Medin>	involves: 129S6/SvEvTac * CD-1	N	23681708
MGI:5800675	M	MP:0009105	penis prolapse	Asah1<tm1Medin>/Asah1<tm1Medin>	involves: 129S6/SvEvTac * CD-1	N	23681708
MGI:5800675	F	MP:0009283	decreased gonadal fat pad weight	Asah1<tm1Medin>/Asah1<tm1Medin>	involves: 129S6/SvEvTac * CD-1	N	23681708
MGI:5800675	F	MP:0011129	decreased tertiary ovarian follicle number	Asah1<tm1Medin>/Asah1<tm1Medin>	involves: 129S6/SvEvTac * CD-1	N	23681708
MGI:5803721	M	MP:0004988	increased osteoblast cell number	Notch2<tm1.1Ecan>/Notch2<+>	involves: 129 * 129S1/Sv * C57BL/6J	N	26627824
MGI:5803721	M	MP:0010933	decreased trabecular bone connectivity density	Notch2<tm1.1Ecan>/Notch2<+>	involves: 129 * 129S1/Sv * C57BL/6J	N	26627824
MGI:5803864	M	MP:0001922	reduced male fertility	Gpx4<tm4Marc>/Gpx4<+>	involves: 129S6/SvEvTac * C57BL/6J	N	25922076
MGI:5803864	M	MP:0002674	abnormal sperm motility	Gpx4<tm4Marc>/Gpx4<+>	involves: 129S6/SvEvTac * C57BL/6J	N	25922076
MGI:5803864	M	MP:0009230	abnormal sperm head morphology	Gpx4<tm4Marc>/Gpx4<+>	involves: 129S6/SvEvTac * C57BL/6J	N	25922076
MGI:5803864	M	MP:0009647	decreased fertilization frequency	Gpx4<tm4Marc>/Gpx4<+>	involves: 129S6/SvEvTac * C57BL/6J	N	25922076
MGI:5803864	M	MP:0009237	kinked sperm flagellum	Gpx4<tm4Marc>/Gpx4<+>	involves: 129S6/SvEvTac * C57BL/6J	N	25922076
MGI:5803864	M	MP:0004543	abnormal sperm physiology	Gpx4<tm4Marc>/Gpx4<+>	involves: 129S6/SvEvTac * C57BL/6J	N	25922076
MGI:5803864	M	MP:0014467	increased sperm mitochondrial size	Gpx4<tm4Marc>/Gpx4<+>	involves: 129S6/SvEvTac * C57BL/6J	N	25922076
MGI:5803864	M	MP:0000242	impaired fertilization	Gpx4<tm4Marc>/Gpx4<+>	involves: 129S6/SvEvTac * C57BL/6J	N	25922076
MGI:5803864	M	MP:0001935	decreased litter size	Gpx4<tm4Marc>/Gpx4<+>	involves: 129S6/SvEvTac * C57BL/6J	N	25922076
MGI:5803864	M	MP:0009831	abnormal sperm midpiece morphology	Gpx4<tm4Marc>/Gpx4<+>	involves: 129S6/SvEvTac * C57BL/6J	N	25922076
MGI:5804449	F	MP:0003212	increased susceptibility to age related obesity	Ldah<tm1Mrtn>/Ldah<tm1Mrtn>	CBACa.129S4(B6)-Ldah<tm1Mrtn>	N	MGI:3606206
MGI:5804449	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Ldah<tm1Mrtn>/Ldah<tm1Mrtn>	CBACa.129S4(B6)-Ldah<tm1Mrtn>	N	MGI:3606206
MGI:5804452	M	MP:0005600	increased heart ventricle muscle contractility	Ednrb<tm1.1Nrd>/Ednrb<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	26240367
MGI:5804452	M	MP:0003027	abnormal blood pH regulation	Ednrb<tm1.1Nrd>/Ednrb<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	26240367
MGI:5804452	M	MP:0003032	hypocapnia	Ednrb<tm1.1Nrd>/Ednrb<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	26240367
MGI:5804452	M	MP:0003394	increased cardiac output	Ednrb<tm1.1Nrd>/Ednrb<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	26240367
MGI:5804452	M	MP:0001574	abnormal oxygen level	Ednrb<tm1.1Nrd>/Ednrb<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	26240367
MGI:5804452	M	MP:0004875	increased mean systemic arterial blood pressure	Ednrb<tm1.1Nrd>/Ednrb<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	26240367
MGI:5804452	M	MP:0004486	decreased response of heart to induced stress	Ednrb<tm1.1Nrd>/Ednrb<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	26240367
MGI:5804452	M	MP:0013404	decreased circulating lactate level	Ednrb<tm1.1Nrd>/Ednrb<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	26240367
MGI:5804568	M	MP:0002631	abnormal epididymis morphology	Adam7<tm1Tigm>/Adam7<tm1Tigm>	involves: C57BL/6	N	26246218
MGI:5804568	M	MP:0000242	impaired fertilization	Adam7<tm1Tigm>/Adam7<tm1Tigm>	involves: C57BL/6	N	26246218
MGI:5804568	M	MP:0002660	abnormal caput epididymis morphology	Adam7<tm1Tigm>/Adam7<tm1Tigm>	involves: C57BL/6	N	26246218
MGI:5804568	M	MP:0002674	abnormal sperm motility	Adam7<tm1Tigm>/Adam7<tm1Tigm>	involves: C57BL/6	N	26246218
MGI:5804568	M	MP:0009824	spermatic granuloma	Adam7<tm1Tigm>/Adam7<tm1Tigm>	involves: C57BL/6	N	26246218
MGI:5804568	M	MP:0001922	reduced male fertility	Adam7<tm1Tigm>/Adam7<tm1Tigm>	involves: C57BL/6	N	26246218
MGI:5804568	M	MP:0004933	abnormal epididymis epithelium morphology	Adam7<tm1Tigm>/Adam7<tm1Tigm>	involves: C57BL/6	N	26246218
MGI:5804568	M	MP:0009237	kinked sperm flagellum	Adam7<tm1Tigm>/Adam7<tm1Tigm>	involves: C57BL/6	N	26246218
MGI:5804568	M	MP:0002662	abnormal cauda epididymis morphology	Adam7<tm1Tigm>/Adam7<tm1Tigm>	involves: C57BL/6	N	26246218
MGI:5804654	M	MP:0001405	impaired coordination	Camkmt<tm1Rpav>/Camkmt<tm1Rpav>	B6.129S7-Camkmt<tm1Rpav>	N	26247364
MGI:5804654	M	MP:0004000	impaired passive avoidance behavior	Camkmt<tm1Rpav>/Camkmt<tm1Rpav>	B6.129S7-Camkmt<tm1Rpav>	N	26247364
MGI:5804654	M	MP:0005369	muscle phenotype	Camkmt<tm1Rpav>/Camkmt<tm1Rpav>	B6.129S7-Camkmt<tm1Rpav>	Y	26247364
MGI:5804654	M	MP:0005386	behavior/neurological phenotype	Camkmt<tm1Rpav>/Camkmt<tm1Rpav>	B6.129S7-Camkmt<tm1Rpav>	Y	26247364
MGI:5804664	F	MP:0004016	decreased bone mass	Tmem178<tm1Lex>/Tmem178<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	26644563
MGI:5804664	F	MP:0004992	increased bone resorption	Tmem178<tm1Lex>/Tmem178<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	26644563
MGI:5804664	F	MP:0003724	increased susceptibility to induced arthritis	Tmem178<tm1Lex>/Tmem178<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	26644563
MGI:5804664	F	MP:0008396	abnormal osteoclast differentiation	Tmem178<tm1Lex>/Tmem178<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	26644563
MGI:5804664	F	MP:0001541	abnormal osteoclast physiology	Tmem178<tm1Lex>/Tmem178<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	26644563
MGI:5804664	F	MP:0010879	decreased trabecular bone volume	Tmem178<tm1Lex>/Tmem178<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	26644563
MGI:5804664	F	MP:0009346	decreased trabecular bone thickness	Tmem178<tm1Lex>/Tmem178<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	26644563
MGI:5804664	F	MP:0004984	increased osteoclast cell number	Tmem178<tm1Lex>/Tmem178<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	26644563
MGI:5804664	F	MP:0010873	decreased trabecular bone mass	Tmem178<tm1Lex>/Tmem178<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	26644563
MGI:5804664	F	MP:0000063	decreased bone mineral density	Tmem178<tm1Lex>/Tmem178<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	26644563
MGI:5805279	F	MP:0013781	abnormal mammary gland luminal epithelium morphology	Id4<tm1Vdr>/Id4<tm1Vdr>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805279	F	MP:0013778	abnormal mammary gland myoepithelium morphology	Id4<tm1Vdr>/Id4<tm1Vdr>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805279	F	MP:0001126	abnormal ovary morphology	Id4<tm1Vdr>/Id4<tm1Vdr>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805279	F	MP:0000662	abnormal branching of the mammary ductal tree	Id4<tm1Vdr>/Id4<tm1Vdr>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805279	F	MP:0013609	abnormal ovarian medulla morphology	Id4<tm1Vdr>/Id4<tm1Vdr>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805279	F	MP:0008870	increased mature ovarian follicle number	Id4<tm1Vdr>/Id4<tm1Vdr>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805279	F	MP:0031239	increased atretic ovarian follicle number	Id4<tm1Vdr>/Id4<tm1Vdr>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805279	F	MP:0001130	abnormal ovarian folliculogenesis	Id4<tm1Vdr>/Id4<tm1Vdr>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805279	F	MP:0011128	increased tertiary ovarian follicle number	Id4<tm1Vdr>/Id4<tm1Vdr>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805279	F	MP:0003371	decreased circulating estrogen level	Id4<tm1Vdr>/Id4<tm1Vdr>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805279	F	MP:0005181	decreased circulating estradiol level	Id4<tm1Vdr>/Id4<tm1Vdr>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805279	F	MP:0031383	increased secondary ovarian follicle number	Id4<tm1Vdr>/Id4<tm1Vdr>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805279	F	MP:0004905	decreased uterus weight	Id4<tm1Vdr>/Id4<tm1Vdr>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805280	F	MP:0000662	abnormal branching of the mammary ductal tree	Id4<tm1Vdr>/Id4<+>,Tg(MMTV-cre)1Mam/0	involves: C57BL/6 * FVB/N	N	25038044
MGI:5805372	F	MP:0003980	increased circulating phospholipid level	Faf2<tm1Tfji>/Faf2<tm1Tfji>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * C57BL/6N * CBA * DBA	N	25970332
MGI:5805372	M	MP:0003981	decreased circulating phospholipid level	Faf2<tm1Tfji>/Faf2<tm1Tfji>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * C57BL/6N * CBA * DBA	N	25970332
MGI:5805375	F	MP:0004856	decreased ovary weight	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	F	MP:0009008	delayed estrous cycle	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	F	MP:0002636	delayed vaginal opening	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	F	MP:0003355	decreased ovulation rate	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	M	MP:0003550	short perineum	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	M	MP:0000837	abnormal hypothalamus morphology	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	F	MP:0009015	short proestrus	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	F	MP:0001751	increased circulating luteinizing hormone level	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	M	MP:0004852	decreased testis weight	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	F	MP:0002680	decreased corpora lutea number	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	F	MP:0005376	homeostasis/metabolism phenotype	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	Y	25248098
MGI:5805375	F	MP:0001923	reduced female fertility	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	M	MP:0002780	decreased circulating testosterone level	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	M	MP:0001922	reduced male fertility	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	M	MP:0001752	abnormal hypothalamus secretion	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805375	F	MP:0001927	abnormal estrous cycle	Dmxl2<tm1c(EUCOMM)Wtsi>/Dmxl2<+>,Tg(Nes-cre)1Atp/0	involves: C57BL/6N * FVB/N	N	25248098
MGI:5805813	M	MP:0005091	increased double-positive T cell number	Prkd2<tm1.1Shoy>/Prkd2<tm1.1Shoy>,Prkd3<tm1.1Shoy>/Prkd3<tm1.1Shoy>,Tg(Lck-cre)1Jtak/0,Tg(TcraH-Y,TcrbH-Y)71Vbo/0	involves: 129 * C57BL/6 * C57BL/6J * DBA/2J	N	27670070
MGI:5805821	M	MP:0004924	abnormal behavior	Pten<tm1Rps>/Pten<+>	B6.129S1-Pten<tm1Rps>/Nci	N	25561290
MGI:5805821	M	MP:0003862	decreased aggression towards male mice	Pten<tm1Rps>/Pten<+>	B6.129S1-Pten<tm1Rps>/Nci	N	25561290
MGI:5805821	M	MP:0001409	increased stereotypic behavior	Pten<tm1Rps>/Pten<+>	B6.129S1-Pten<tm1Rps>/Nci	N	25561290
MGI:5805821	M	MP:0001360	abnormal social investigation	Pten<tm1Rps>/Pten<+>	B6.129S1-Pten<tm1Rps>/Nci	N	25561290
MGI:5805833	M	MP:0001222	epidermal hyperplasia	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0009441	delayed skin barrier formation	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0010683	dilated hair follicle infundibulum	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0010682	abnormal hair follicle infundibulum morphology	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0009759	abnormal hair follicle bulge morphology	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0011939	increased food intake	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0014169	decreased brown adipose tissue mass	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0002073	abnormal hair growth	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0006042	increased apoptosis	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0000377	abnormal hair follicle morphology	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0000414	alopecia	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0001240	abnormal epidermis stratum corneum morphology	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0009293	decreased inguinal fat pad weight	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0003704	abnormal hair follicle development	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0001239	abnormal epidermis stratum granulosum morphology	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0009535	abnormal skin sebaceous gland morphology	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0004889	increased energy expenditure	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0001399	hyperactivity	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0001245	thick dermal layer	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0009823	abnormal sphingomyelin level	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0005011	increased eosinophil cell number	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0004947	skin inflammation	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0001192	scaly skin	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0009583	increased keratinocyte proliferation	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0009288	increased epididymal fat pad weight	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0001547	abnormal lipid level	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0002796	impaired skin barrier function	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0003809	abnormal hair shaft morphology	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0003810	abnormal hair cuticle	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0020117	decreased sphingosine level	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0009289	decreased epididymal fat pad weight	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0000400	abnormal awl hair morphology	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0013375	abnormal sebocyte morphology	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0000402	abnormal zigzag hair morphology	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0009602	abnormal keratohyalin granule morphology	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0001242	hyperkeratosis	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0012232	abnormal ceramide level	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0000367	abnormal coat/ hair morphology	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0000652	enlarged sebaceous gland	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0009125	decreased brown fat cell lipid droplet size	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0001262	decreased body weight	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0003853	dry skin	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805833	M	MP:0008965	increased basal metabolism	Acer1<tm1a(EUCOMM)Wtsi>/Acer1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Acer1<tm1a(EUCOMM)Wtsi>	N	27126290
MGI:5805971	F	MP:0000609	abnormal liver physiology	Hoga1<tm2a(KOMP)Wtsi>/Hoga1<tm2a(KOMP)Wtsi>	involves: C57BL/6N	N	26428388
MGI:5805971	F	MP:0009642	abnormal blood homeostasis	Hoga1<tm2a(KOMP)Wtsi>/Hoga1<tm2a(KOMP)Wtsi>	involves: C57BL/6N	N	26428388
MGI:5805971	M	MP:0009643	abnormal urine homeostasis	Hoga1<tm2a(KOMP)Wtsi>/Hoga1<tm2a(KOMP)Wtsi>	involves: C57BL/6N	N	26428388
MGI:5805971	F	MP:0009643	abnormal urine homeostasis	Hoga1<tm2a(KOMP)Wtsi>/Hoga1<tm2a(KOMP)Wtsi>	involves: C57BL/6N	N	26428388
MGI:5806085	M	MP:0003068	enlarged kidney	Slc41a3<tm1a(KOMP)Wtsi>/Slc41a3<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27349617
MGI:5806085	M	MP:0003588	ureter stenosis	Slc41a3<tm1a(KOMP)Wtsi>/Slc41a3<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27349617
MGI:5806085	M	MP:0000519	hydronephrosis	Slc41a3<tm1a(KOMP)Wtsi>/Slc41a3<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27349617
MGI:5806128	M	MP:0001363	increased anxiety-related response	Hgsnat<tm1a(EUCOMM)Wtsi>/Hgsnat<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N * C57BL/6NTac	N	27491071
MGI:5806128	M	MP:0001402	decreased locomotor activity	Hgsnat<tm1a(EUCOMM)Wtsi>/Hgsnat<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N * C57BL/6NTac	N	27491071
MGI:5806227	M	MP:0001922	reduced male fertility	Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: C57BL/6 * CBA	N	26306493
MGI:5806227	M	MP:0001935	decreased litter size	Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: C57BL/6 * CBA	N	26306493
MGI:5806227	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: C57BL/6 * CBA	N	26306493
MGI:5806227	M	MP:0001932	abnormal spermiogenesis	Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: C57BL/6 * CBA	N	26306493
MGI:5806227	M	MP:0009232	abnormal sperm nucleus morphology	Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: C57BL/6 * CBA	N	26306493
MGI:5806227	M	MP:0002687	oligozoospermia	Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: C57BL/6 * CBA	N	26306493
MGI:5806227	M	MP:0002686	globozoospermia	Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: C57BL/6 * CBA	N	26306493
MGI:5806228	M	MP:0009232	abnormal sperm nucleus morphology	Ica1<tm1Mdos>/Ica1<tm1Mdos>,Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	26306493
MGI:5806228	M	MP:0002686	globozoospermia	Ica1<tm1Mdos>/Ica1<tm1Mdos>,Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	26306493
MGI:5806228	M	MP:0002687	oligozoospermia	Ica1<tm1Mdos>/Ica1<tm1Mdos>,Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	26306493
MGI:5806228	M	MP:0008898	abnormal acrosome morphology	Ica1<tm1Mdos>/Ica1<tm1Mdos>,Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	26306493
MGI:5806228	M	MP:0001932	abnormal spermiogenesis	Ica1<tm1Mdos>/Ica1<tm1Mdos>,Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	26306493
MGI:5806228	M	MP:0008839	absent acrosome	Ica1<tm1Mdos>/Ica1<tm1Mdos>,Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	26306493
MGI:5806228	M	MP:0001925	male infertility	Ica1<tm1Mdos>/Ica1<tm1Mdos>,Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	26306493
MGI:5806228	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Ica1<tm1Mdos>/Ica1<tm1Mdos>,Ica1l<em1Jxia>/Ica1l<em1Jxia>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	N	26306493
MGI:5806238	F	MP:0005459	decreased percent body fat/body weight	Lypd3<tm1(KOMP)Vlcg>/Lypd3<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	27169360
MGI:5806238	F	MP:0002006	neoplasm	Lypd3<tm1(KOMP)Vlcg>/Lypd3<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	Y	27169360
MGI:5806238	F	MP:0014143	decreased body fat mass	Lypd3<tm1(KOMP)Vlcg>/Lypd3<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	27169360
MGI:5806238	F	MP:0008853	decreased abdominal adipose tissue amount	Lypd3<tm1(KOMP)Vlcg>/Lypd3<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	27169360
MGI:5806238	F	MP:0004502	decreased incidence of tumors by chemical induction	Lypd3<tm1(KOMP)Vlcg>/Lypd3<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	27169360
MGI:5806238	F	MP:0008844	decreased subcutaneous adipose tissue amount	Lypd3<tm1(KOMP)Vlcg>/Lypd3<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	27169360
MGI:5806238	M	MP:0002908	delayed wound healing	Lypd3<tm1(KOMP)Vlcg>/Lypd3<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	27169360
MGI:5806238	F	MP:0011940	decreased food intake	Lypd3<tm1(KOMP)Vlcg>/Lypd3<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	27169360
MGI:5806244	F	MP:0011895	abnormal circulating unsaturated transferrin level	Ndfip2<tm1a(EUCOMM)Hmgu>/Ndfip2<tm1a(EUCOMM)Hmgu>	C57BL/6N-Ndfip2<tm1a(EUCOMM)Hmgu>	N	27048792
MGI:5806244	F	MP:0005637	abnormal iron homeostasis	Ndfip2<tm1a(EUCOMM)Hmgu>/Ndfip2<tm1a(EUCOMM)Hmgu>	C57BL/6N-Ndfip2<tm1a(EUCOMM)Hmgu>	N	27048792
MGI:5806244	F	MP:0004152	abnormal circulating iron level	Ndfip2<tm1a(EUCOMM)Hmgu>/Ndfip2<tm1a(EUCOMM)Hmgu>	C57BL/6N-Ndfip2<tm1a(EUCOMM)Hmgu>	N	27048792
MGI:5806244	F	MP:0008743	decreased liver iron level	Ndfip2<tm1a(EUCOMM)Hmgu>/Ndfip2<tm1a(EUCOMM)Hmgu>	C57BL/6N-Ndfip2<tm1a(EUCOMM)Hmgu>	N	27048792
MGI:5806244	F	MP:0008807	increased liver iron level	Ndfip2<tm1a(EUCOMM)Hmgu>/Ndfip2<tm1a(EUCOMM)Hmgu>	C57BL/6N-Ndfip2<tm1a(EUCOMM)Hmgu>	N	27048792
MGI:5806244	M	MP:0008738	abnormal liver iron level	Ndfip2<tm1a(EUCOMM)Hmgu>/Ndfip2<tm1a(EUCOMM)Hmgu>	C57BL/6N-Ndfip2<tm1a(EUCOMM)Hmgu>	N	27048792
MGI:5806429	M	MP:0001559	hyperglycemia	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0013279	increased fasting circulating glucose level	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0030009	increased bone marrow adipose tissue amount	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0005017	decreased B cell number	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0000221	decreased leukocyte cell number	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0000220	increased monocyte cell number	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0009338	increased splenocyte number	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0008121	increased myeloid dendritic cell number	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0000063	decreased bone mineral density	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0013693	abnormal hemopoiesis	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0005425	increased macrophage cell number	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0009285	increased gonadal fat pad weight	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0001260	increased body weight	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0005014	increased B cell number	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0005331	insulin resistance	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0030007	abnormal bone marrow adipose tissue morphology	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0010879	decreased trabecular bone volume	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806429	M	MP:0000222	decreased neutrophil cell number	Mfap2<tm1a(KOMP)Wtsi>/Mfap2<tm1a(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	27445989
MGI:5806467	M	MP:0001869	pancreas inflammation	X/Tg(Ela-KRAS*G12D)9Eps	involves: C57BL/6 * FVB	N	26980767
MGI:5806467	M	MP:0009146	abnormal pancreatic acinar cell morphology	X/Tg(Ela-KRAS*G12D)9Eps	involves: C57BL/6 * FVB	N	26980767
MGI:5806467	M	MP:0004973	increased regulatory T cell number	X/Tg(Ela-KRAS*G12D)9Eps	involves: C57BL/6 * FVB	N	26980767
MGI:5806467	M	MP:0001944	abnormal pancreas morphology	X/Tg(Ela-KRAS*G12D)9Eps	involves: C57BL/6 * FVB	N	26980767
MGI:5806467	M	MP:0013221	pancreatic acinar-to-ductal metaplasia	X/Tg(Ela-KRAS*G12D)9Eps	involves: C57BL/6 * FVB	N	26980767
MGI:5806467	M	MP:0009153	increased pancreas tumor incidence	X/Tg(Ela-KRAS*G12D)9Eps	involves: C57BL/6 * FVB	N	26980767
MGI:5806467	M	MP:0013584	pancreas degeneration	X/Tg(Ela-KRAS*G12D)9Eps	involves: C57BL/6 * FVB	N	26980767
MGI:5806468	M	MP:0003334	pancreas fibrosis	X/Tg(Ela-KRAS*G12D)9Eps,Tg(Mt1-TGFBR2*)AM3Epb/0	involves: C57BL/6 * FVB	N	26980767
MGI:5806468	M	MP:0001944	abnormal pancreas morphology	X/Tg(Ela-KRAS*G12D)9Eps,Tg(Mt1-TGFBR2*)AM3Epb/0	involves: C57BL/6 * FVB	N	26980767
MGI:5806468	M	MP:0001869	pancreas inflammation	X/Tg(Ela-KRAS*G12D)9Eps,Tg(Mt1-TGFBR2*)AM3Epb/0	involves: C57BL/6 * FVB	N	26980767
MGI:5806468	M	MP:0004973	increased regulatory T cell number	X/Tg(Ela-KRAS*G12D)9Eps,Tg(Mt1-TGFBR2*)AM3Epb/0	involves: C57BL/6 * FVB	N	26980767
MGI:5806468	M	MP:0013221	pancreatic acinar-to-ductal metaplasia	X/Tg(Ela-KRAS*G12D)9Eps,Tg(Mt1-TGFBR2*)AM3Epb/0	involves: C57BL/6 * FVB	N	26980767
MGI:5806468	M	MP:0002693	abnormal pancreas physiology	X/Tg(Ela-KRAS*G12D)9Eps,Tg(Mt1-TGFBR2*)AM3Epb/0	involves: C57BL/6 * FVB	N	26980767
MGI:5806468	M	MP:0009153	increased pancreas tumor incidence	X/Tg(Ela-KRAS*G12D)9Eps,Tg(Mt1-TGFBR2*)AM3Epb/0	involves: C57BL/6 * FVB	N	26980767
MGI:5806470	M	MP:0002693	abnormal pancreas physiology	X/Tg(Ela-KRAS*G12D)9Eps,Tgfbr1<tm1Bopa>/Tgfbr1<+>	involves: 129S1/SvImJ * C57BL/6 * FVB	N	26980767
MGI:5806470	M	MP:0008078	increased CD8-positive, alpha-beta T cell number	X/Tg(Ela-KRAS*G12D)9Eps,Tgfbr1<tm1Bopa>/Tgfbr1<+>	involves: 129S1/SvImJ * C57BL/6 * FVB	N	26980767
MGI:5806470	M	MP:0009153	increased pancreas tumor incidence	X/Tg(Ela-KRAS*G12D)9Eps,Tgfbr1<tm1Bopa>/Tgfbr1<+>	involves: 129S1/SvImJ * C57BL/6 * FVB	N	26980767
MGI:5806471	M	MP:0012416	decreased gland tumor incidence	X/Tg(Ela-KRAS*G12D)9Eps,Tgfbr1<tm1Bopa>/Tgfbr1<+>,Tg(Mt1-TGFBR2*)AM3Epb/0	involves: 129S1/SvImJ * C57BL/6 * FVB	N	26980767
MGI:5806513	M	MP:0001925	male infertility	Kbtbd2<m1Btlr>/Kbtbd2<m1Btlr>	C57BL/6J-Kbtbd2<m1Btlr>	N	27708159
MGI:5806513	F	MP:0001926	female infertility	Kbtbd2<m1Btlr>/Kbtbd2<m1Btlr>	C57BL/6J-Kbtbd2<m1Btlr>	N	27708159
MGI:5806514	M	MP:0013279	increased fasting circulating glucose level	Kbtbd2<em1Btlr>/Kbtbd2<em1Btlr>	Not Specified	N	27708159
MGI:5806514	M	MP:0005331	insulin resistance	Kbtbd2<em1Btlr>/Kbtbd2<em1Btlr>	Not Specified	N	27708159
MGI:5806514	M	MP:0002079	increased circulating insulin level	Kbtbd2<em1Btlr>/Kbtbd2<em1Btlr>	Not Specified	N	27708159
MGI:5806514	M	MP:0001262	decreased body weight	Kbtbd2<em1Btlr>/Kbtbd2<em1Btlr>	Not Specified	N	27708159
MGI:5806515	M	MP:0002727	decreased circulating insulin level	Kbtbd2<em1Btlr>/Kbtbd2<em1Btlr>,Pik3r1<em1Btlr>/Pik3r1<em1Btlr>	Not Specified	N	27708159
MGI:5806515	M	MP:0002891	increased insulin sensitivity	Kbtbd2<em1Btlr>/Kbtbd2<em1Btlr>,Pik3r1<em1Btlr>/Pik3r1<em1Btlr>	Not Specified	N	27708159
MGI:5806515	M	MP:0001260	increased body weight	Kbtbd2<em1Btlr>/Kbtbd2<em1Btlr>,Pik3r1<em1Btlr>/Pik3r1<em1Btlr>	Not Specified	N	27708159
MGI:5806515	M	MP:0014142	increased body fat mass	Kbtbd2<em1Btlr>/Kbtbd2<em1Btlr>,Pik3r1<em1Btlr>/Pik3r1<em1Btlr>	Not Specified	N	27708159
MGI:5806515	M	MP:0005560	decreased circulating glucose level	Kbtbd2<em1Btlr>/Kbtbd2<em1Btlr>,Pik3r1<em1Btlr>/Pik3r1<em1Btlr>	Not Specified	N	27708159
MGI:5806886	M	MP:0006138	congestive heart failure	Cap2<tm1a(EUCOMM)Wtsi>/Cap2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26616005
MGI:5806886	M	MP:0005608	cardiac interstitial fibrosis	Cap2<tm1a(EUCOMM)Wtsi>/Cap2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26616005
MGI:5806886	M	MP:0001320	small pupil	Cap2<tm1a(EUCOMM)Wtsi>/Cap2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26616005
MGI:5806886	M	MP:0003061	decreased aerobic running capacity	Cap2<tm1a(EUCOMM)Wtsi>/Cap2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26616005
MGI:5806886	M	MP:0011086	postnatal lethality, incomplete penetrance	Cap2<tm1a(EUCOMM)Wtsi>/Cap2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26616005
MGI:5806886	M	MP:0031633	decreased heart left ventricle muscle contractility	Cap2<tm1a(EUCOMM)Wtsi>/Cap2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26616005
MGI:5806886	M	MP:0008770	decreased survivor rate	Cap2<tm1a(EUCOMM)Wtsi>/Cap2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26616005
MGI:5806886	M	MP:0002753	dilated heart left ventricle	Cap2<tm1a(EUCOMM)Wtsi>/Cap2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26616005
MGI:5806886	M	MP:0001297	microphthalmia	Cap2<tm1a(EUCOMM)Wtsi>/Cap2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26616005
MGI:5806888	M	MP:0008770	decreased survivor rate	Cap2<tm1a(EUCOMM)Wtsi>/Cap2<+>	involves: C57BL/6J * C57BL/6N	N	26616005
MGI:5806892	M	MP:0002169	no abnormal phenotype detected	Cap2<tm1c(EUCOMM)Wtsi>/Cap2<tm1c(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	26616005
MGI:5806920	F	MP:0020946	increased susceptibility to Orthomyxoviridae infection	Lst1<tm1(KOMP)Vlcg>/Lst1<tm1(KOMP)Vlcg>	C57BL/6N-Lst1<tm1(KOMP)Vlcg>	N	26817701
MGI:5806920	F	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality	Lst1<tm1(KOMP)Vlcg>/Lst1<tm1(KOMP)Vlcg>	C57BL/6N-Lst1<tm1(KOMP)Vlcg>	N	26817701
MGI:5806920	M	MP:0005387	immune system phenotype	Lst1<tm1(KOMP)Vlcg>/Lst1<tm1(KOMP)Vlcg>	C57BL/6N-Lst1<tm1(KOMP)Vlcg>	Y	26817701
MGI:5807153	M	MP:0005376	homeostasis/metabolism phenotype	Lep<ob>/Lep<ob>	B6.Cg-Lep<ob>/JRj	Y	22118645
MGI:5807153	M	MP:0001260	increased body weight	Lep<ob>/Lep<ob>	B6.Cg-Lep<ob>/JRj	N	22118645
MGI:5807153	M	MP:0003333	liver fibrosis	Lep<ob>/Lep<ob>	B6.Cg-Lep<ob>/JRj	N	22118645
MGI:5807153	M	MP:0002628	hepatic steatosis	Lep<ob>/Lep<ob>	B6.Cg-Lep<ob>/JRj	N	22118645
MGI:5807153	M	MP:0003982	increased cholesterol level	Lep<ob>/Lep<ob>	B6.Cg-Lep<ob>/JRj	N	22118645
MGI:5807153	M	MP:0003887	increased hepatocyte apoptosis	Lep<ob>/Lep<ob>	B6.Cg-Lep<ob>/JRj	N	22118645
MGI:5807153	M	MP:0005658	increased susceptibility to diet-induced obesity	Lep<ob>/Lep<ob>	B6.Cg-Lep<ob>/JRj	N	22118645
MGI:5807153	M	MP:0001860	liver inflammation	Lep<ob>/Lep<ob>	B6.Cg-Lep<ob>/JRj	N	22118645
MGI:5807153	M	MP:0001554	increased circulating free fatty acids level	Lep<ob>/Lep<ob>	B6.Cg-Lep<ob>/JRj	N	22118645
MGI:5807359	M	MP:0002169	no abnormal phenotype detected	Slc6a14<tm1Gana>/Y	Not Specified	Y	26173258
MGI:5807360	F	MP:0005379	endocrine/exocrine gland phenotype	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>	Not Specified	Y	26173258
MGI:5807360	F	MP:0010210	abnormal circulating cytokine level	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>	Not Specified	N	26173258
MGI:5807360	F	MP:0008603	decreased circulating interleukin-4 level	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>	Not Specified	N	26173258
MGI:5807360	F	MP:0005376	homeostasis/metabolism phenotype	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>	Not Specified	Y	26173258
MGI:5807360	F	MP:0010209	abnormal circulating chemokine level	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>	Not Specified	N	26173258
MGI:5807360	F	MP:0008639	decreased circulating interleukin-1 alpha level	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>	Not Specified	N	26173258
MGI:5807361	F	MP:0003447	decreased tumor growth/size	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>,Tg(MMTV-PyVT)634Mul/0	Not Specified	N	26173258
MGI:5807361	F	MP:0005332	abnormal amino acid level	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>,Tg(MMTV-PyVT)634Mul/0	Not Specified	N	26173258
MGI:5807361	F	MP:0009828	increased tumor latency	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>,Tg(MMTV-PyVT)634Mul/0	Not Specified	N	26173258
MGI:5807361	F	MP:0002490	abnormal immunoglobulin level	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>,Tg(MMTV-PyVT)634Mul/0	Not Specified	N	26173258
MGI:5807361	F	MP:0001273	decreased metastatic potential	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>,Tg(MMTV-PyVT)634Mul/0	Not Specified	N	26173258
MGI:5807362	F	MP:0009828	increased tumor latency	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>,Tg(MMTVneu)202Mul/0	involves: FVB/N	N	26173258
MGI:5807362	F	MP:0003447	decreased tumor growth/size	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>,Tg(MMTVneu)202Mul/0	involves: FVB/N	N	26173258
MGI:5807362	F	MP:0010269	decreased mammary gland tumor incidence	Slc6a14<tm1Gana>/Slc6a14<tm1Gana>,Tg(MMTVneu)202Mul/0	involves: FVB/N	N	26173258
MGI:5807457	F	MP:0001926	female infertility	Izumo1r<tm1a(KOMP)Wtsi>/Izumo1r<tm1a(KOMP)Wtsi>	involves: C57BL/6N * C57BL/6NTac	N	24739963
MGI:5807466	F	MP:0001926	female infertility	Izumo1r<tm2a(KOMP)Wtsi>/Izumo1r<tm2a(KOMP)Wtsi>	involves: C57BL/6N	N	24739963
MGI:5810083	F	MP:0013781	abnormal mammary gland luminal epithelium morphology	Skil<tm2Spw>/Skil<tm2Spw>	involves: 129S1/Sv * 129X1/SvJ	N	22833129
MGI:5810083	F	MP:0012075	impaired mammary gland growth during pregnancy	Skil<tm2Spw>/Skil<tm2Spw>	involves: 129S1/Sv * 129X1/SvJ	N	22833129
MGI:5810083	F	MP:0009504	abnormal mammary gland epithelium morphology	Skil<tm2Spw>/Skil<tm2Spw>	involves: 129S1/Sv * 129X1/SvJ	N	22833129
MGI:5810083	F	MP:0006270	abnormal mammary gland growth during lactation	Skil<tm2Spw>/Skil<tm2Spw>	involves: 129S1/Sv * 129X1/SvJ	N	22833129
MGI:5810083	F	MP:0013716	hypolactation	Skil<tm2Spw>/Skil<tm2Spw>	involves: 129S1/Sv * 129X1/SvJ	N	22833129
MGI:5810083	F	MP:0009506	abnormal mammary gland alveolus morphology	Skil<tm2Spw>/Skil<tm2Spw>	involves: 129S1/Sv * 129X1/SvJ	N	22833129
MGI:5810083	F	MP:0001881	abnormal mammary gland physiology	Skil<tm2Spw>/Skil<tm2Spw>	involves: 129S1/Sv * 129X1/SvJ	N	22833129
MGI:5810107	M	MP:0009451	abnormal chromosomal synapsis	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	M	MP:0004901	decreased male germ cell number	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	M	MP:0001153	small seminiferous tubules	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	F	MP:0001931	abnormal oogenesis	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	F	MP:0001926	female infertility	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	M	MP:0030024	abnormal meiotic attachment of telomere to nuclear envelope	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	M	MP:0002216	abnormal seminiferous tubule morphology	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	M	MP:0013601	increased testis apoptosis	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	M	MP:0010948	abnormal double-strand DNA break repair	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	M	MP:0001925	male infertility	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	M	MP:0006379	abnormal spermatocyte morphology	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	M	MP:0001147	small testis	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	M	MP:0008261	arrest of male meiosis	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	F	MP:0001127	small ovary	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810107	F	MP:0002777	absent ovarian follicles	Kash5<tm1b(KOMP)Wtsi>/Kash5<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	24062341
MGI:5810170	M	MP:0000278	abnormal myocardial fiber morphology	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0008725	increased heart atrium size	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0008260	abnormal autophagy	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0010725	thin interventricular septum	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0008772	increased heart ventricle size	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0005140	decreased cardiac muscle contractility	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0002083	premature death	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0021158	decreased heart left ventricle wall thickness	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0005598	decreased heart ventricle muscle contractility	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0003222	increased cardiomyocyte apoptosis	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0004565	decreased myocardial fiber size	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0004090	abnormal sarcomere morphology	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0005608	cardiac interstitial fibrosis	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0006036	abnormal mitochondrial physiology	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0006138	congestive heart failure	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0013272	abnormal translation	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0010334	pleural effusion	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0000274	enlarged heart	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0004485	increased response of heart to induced stress	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0002795	dilated cardiomyopathy	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0005324	ascites	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0004215	abnormal myocardial fiber physiology	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810170	M	MP:0011632	dilated mitochondrion	Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	20644257
MGI:5810171	M	MP:0005599	increased cardiac muscle contractility	Eif4ebp1<tm1Nso>/Eif4ebp1<tm1Nso>	involves: 129S4/SvJae * C57BL/6	N	20644257
MGI:5810171	M	MP:0004215	abnormal myocardial fiber physiology	Eif4ebp1<tm1Nso>/Eif4ebp1<tm1Nso>	involves: 129S4/SvJae * C57BL/6	N	20644257
MGI:5810178	M	MP:0003223	decreased cardiomyocyte apoptosis	Eif4ebp1<tm1Nso>/Eif4ebp1<tm1Nso>,Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	20644257
MGI:5810178	M	MP:0008260	abnormal autophagy	Eif4ebp1<tm1Nso>/Eif4ebp1<tm1Nso>,Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	20644257
MGI:5810178	M	MP:0005385	cardiovascular system phenotype	Eif4ebp1<tm1Nso>/Eif4ebp1<tm1Nso>,Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S4/SvJae * C57BL/6 * FVB/N	Y	20644257
MGI:5810178	M	MP:0005608	cardiac interstitial fibrosis	Eif4ebp1<tm1Nso>/Eif4ebp1<tm1Nso>,Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	20644257
MGI:5810178	M	MP:0002083	premature death	Eif4ebp1<tm1Nso>/Eif4ebp1<tm1Nso>,Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	20644257
MGI:5810178	M	MP:0006036	abnormal mitochondrial physiology	Eif4ebp1<tm1Nso>/Eif4ebp1<tm1Nso>,Mtor<tm1.1Gcon>/Mtor<tm1.1Gcon>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	20644257
MGI:5811279	M	MP:0003224	neuron degeneration	Pitrm1<tm1a(KOMP)Wtsi>/Pitrm1<+>	C57BL/6N-Pitrm1<tm1a(KOMP)Wtsi>/Wtsi	N	26697887
MGI:5811279	M	MP:0001516	abnormal motor coordination/balance	Pitrm1<tm1a(KOMP)Wtsi>/Pitrm1<+>	C57BL/6N-Pitrm1<tm1a(KOMP)Wtsi>/Wtsi	N	26697887
MGI:5811279	M	MP:0005290	decreased oxygen consumption	Pitrm1<tm1a(KOMP)Wtsi>/Pitrm1<+>	C57BL/6N-Pitrm1<tm1a(KOMP)Wtsi>/Wtsi	N	26697887
MGI:5811279	M	MP:0006036	abnormal mitochondrial physiology	Pitrm1<tm1a(KOMP)Wtsi>/Pitrm1<+>	C57BL/6N-Pitrm1<tm1a(KOMP)Wtsi>/Wtsi	N	26697887
MGI:5811279	M	MP:0002183	gliosis	Pitrm1<tm1a(KOMP)Wtsi>/Pitrm1<+>	C57BL/6N-Pitrm1<tm1a(KOMP)Wtsi>/Wtsi	N	26697887
MGI:5811279	M	MP:0008964	decreased carbon dioxide production	Pitrm1<tm1a(KOMP)Wtsi>/Pitrm1<+>	C57BL/6N-Pitrm1<tm1a(KOMP)Wtsi>/Wtsi	N	26697887
MGI:5811279	M	MP:0003329	amyloid beta deposits	Pitrm1<tm1a(KOMP)Wtsi>/Pitrm1<+>	C57BL/6N-Pitrm1<tm1a(KOMP)Wtsi>/Wtsi	N	26697887
MGI:5811279	M	MP:0005356	positive geotaxis	Pitrm1<tm1a(KOMP)Wtsi>/Pitrm1<+>	C57BL/6N-Pitrm1<tm1a(KOMP)Wtsi>/Wtsi	N	26697887
MGI:5811279	M	MP:0001405	impaired coordination	Pitrm1<tm1a(KOMP)Wtsi>/Pitrm1<+>	C57BL/6N-Pitrm1<tm1a(KOMP)Wtsi>/Wtsi	N	26697887
MGI:5811279	M	MP:0002757	decreased vertical activity	Pitrm1<tm1a(KOMP)Wtsi>/Pitrm1<+>	C57BL/6N-Pitrm1<tm1a(KOMP)Wtsi>/Wtsi	N	26697887
MGI:5811279	M	MP:0001393	ataxia	Pitrm1<tm1a(KOMP)Wtsi>/Pitrm1<+>	C57BL/6N-Pitrm1<tm1a(KOMP)Wtsi>/Wtsi	N	26697887
MGI:5811279	M	MP:0020234	decreased basal metabolism	Pitrm1<tm1a(KOMP)Wtsi>/Pitrm1<+>	C57BL/6N-Pitrm1<tm1a(KOMP)Wtsi>/Wtsi	N	26697887
MGI:5811794	M	MP:0003459	increased fear-related response	St3gal4<tm1.1Bsi>/St3gal4<tm1.1Bsi>	B6J.B6N-St3gal4<tm1.1Bsi>	N	25066807
MGI:5811794	M	MP:0003063	increased coping response	St3gal4<tm1.1Bsi>/St3gal4<tm1.1Bsi>	B6J.B6N-St3gal4<tm1.1Bsi>	N	25066807
MGI:5811794	M	MP:0008831	abnormal insulin-like growth factor I level	St3gal4<tm1.1Bsi>/St3gal4<tm1.1Bsi>	B6J.B6N-St3gal4<tm1.1Bsi>	N	25066807
MGI:5811794	M	MP:0001500	decreased kindling response	St3gal4<tm1.1Bsi>/St3gal4<tm1.1Bsi>	B6J.B6N-St3gal4<tm1.1Bsi>	N	25066807
MGI:5811794	M	MP:0001363	increased anxiety-related response	St3gal4<tm1.1Bsi>/St3gal4<tm1.1Bsi>	B6J.B6N-St3gal4<tm1.1Bsi>	N	25066807
MGI:5811794	M	MP:0002573	behavioral despair	St3gal4<tm1.1Bsi>/St3gal4<tm1.1Bsi>	B6J.B6N-St3gal4<tm1.1Bsi>	N	25066807
MGI:5811794	M	MP:0002806	abnormal conditioned emotional response	St3gal4<tm1.1Bsi>/St3gal4<tm1.1Bsi>	B6J.B6N-St3gal4<tm1.1Bsi>	N	25066807
MGI:5811794	M	MP:0005136	decreased growth hormone level	St3gal4<tm1.1Bsi>/St3gal4<tm1.1Bsi>	B6J.B6N-St3gal4<tm1.1Bsi>	N	25066807
MGI:5811794	M	MP:0001501	abnormal sleep pattern	St3gal4<tm1.1Bsi>/St3gal4<tm1.1Bsi>	B6J.B6N-St3gal4<tm1.1Bsi>	N	25066807
MGI:5811794	M	MP:0012286	decreased frequency of paradoxical sleep	St3gal4<tm1.1Bsi>/St3gal4<tm1.1Bsi>	B6J.B6N-St3gal4<tm1.1Bsi>	N	25066807
MGI:5811989	M	MP:0001441	increased grooming behavior	Arhgap32<tm1Taki>/Arhgap32<tm1Taki>	B6N.Cg-Arhgap32<tm1Taki>	N	26979507
MGI:5811989	M	MP:0002906	increased susceptibility to pharmacologically induced seizures	Arhgap32<tm1Taki>/Arhgap32<tm1Taki>	B6N.Cg-Arhgap32<tm1Taki>	N	26979507
MGI:5811989	M	MP:0011622	abnormal habituation to a novel odor	Arhgap32<tm1Taki>/Arhgap32<tm1Taki>	B6N.Cg-Arhgap32<tm1Taki>	N	26979507
MGI:5811989	M	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude	Arhgap32<tm1Taki>/Arhgap32<tm1Taki>	B6N.Cg-Arhgap32<tm1Taki>	N	26979507
MGI:5811989	M	MP:0021117	abnormal huddling behavior	Arhgap32<tm1Taki>/Arhgap32<tm1Taki>	B6N.Cg-Arhgap32<tm1Taki>	N	26979507
MGI:5811989	M	MP:0001405	impaired coordination	Arhgap32<tm1Taki>/Arhgap32<tm1Taki>	B6N.Cg-Arhgap32<tm1Taki>	N	26979507
MGI:5811989	M	MP:0003863	decreased aggression towards mice	Arhgap32<tm1Taki>/Arhgap32<tm1Taki>	B6N.Cg-Arhgap32<tm1Taki>	N	26979507
MGI:5811989	M	MP:0020395	abnormal response to social novelty	Arhgap32<tm1Taki>/Arhgap32<tm1Taki>	B6N.Cg-Arhgap32<tm1Taki>	N	26979507
MGI:5811989	M	MP:0001409	increased stereotypic behavior	Arhgap32<tm1Taki>/Arhgap32<tm1Taki>	B6N.Cg-Arhgap32<tm1Taki>	N	26979507
MGI:5811989	M	MP:0012315	impaired learning	Arhgap32<tm1Taki>/Arhgap32<tm1Taki>	B6N.Cg-Arhgap32<tm1Taki>	N	26979507
MGI:5811989	M	MP:0001360	abnormal social investigation	Arhgap32<tm1Taki>/Arhgap32<tm1Taki>	B6N.Cg-Arhgap32<tm1Taki>	N	26979507
MGI:5812398	M	MP:0008770	decreased survivor rate	Lncpint<tm1Vlcg>/Lncpint<tm1Vlcg>	involves: 129S6/SvEvTac * C57BL/6NTac	N	25909911
MGI:5812398	M	MP:0003961	decreased lean body mass	Lncpint<tm1Vlcg>/Lncpint<tm1Vlcg>	involves: 129S6/SvEvTac * C57BL/6NTac	N	25909911
MGI:5812401	M	MP:0001262	decreased body weight	Lncpint<tm1Vlcg>/Lncpint<+>	involves: 129S6/SvEvTac * C57BL/6NTac	N	25909911
MGI:5812401	M	MP:0001732	postnatal growth retardation	Lncpint<tm1Vlcg>/Lncpint<+>	involves: 129S6/SvEvTac * C57BL/6NTac	N	25909911
MGI:5812899	M	MP:0000272	abnormal aorta morphology	Atf4<tm1.1Cmad>/Atf4<tm1.1Cmad>,Tg(Myh11-icre/ERT2)1Soff/?	D2.Cg-Atf4<tm1.1Cmad> Tg(Myh11-icre/ERT2)1Soff	N	27812542
MGI:5812899	M	MP:0005376	homeostasis/metabolism phenotype	Atf4<tm1.1Cmad>/Atf4<tm1.1Cmad>,Tg(Myh11-icre/ERT2)1Soff/?	D2.Cg-Atf4<tm1.1Cmad> Tg(Myh11-icre/ERT2)1Soff	Y	27812542
MGI:5812899	M	MP:0004231	abnormal calcium ion homeostasis	Atf4<tm1.1Cmad>/Atf4<tm1.1Cmad>,Tg(Myh11-icre/ERT2)1Soff/?	D2.Cg-Atf4<tm1.1Cmad> Tg(Myh11-icre/ERT2)1Soff	N	27812542
MGI:5812901	M	MP:0010522	calcified aorta	Gt(ROSA)26Sor<tm2(ATF4)Myz>/Gt(ROSA)26Sor<tm2(ATF4)Myz>,Tg(Myh11-icre/ERT2)1Soff/?	either: D2.Cg-Atf4<tm1.1Cmad> Tg(Myh11-icre/ERT2)1Soff or B6.Cg-Atf4<tm1.1Cmad> Tg(Myh11-icre/ERT2)1Soff	N	27812542
MGI:5812901	M	MP:0003222	increased cardiomyocyte apoptosis	Gt(ROSA)26Sor<tm2(ATF4)Myz>/Gt(ROSA)26Sor<tm2(ATF4)Myz>,Tg(Myh11-icre/ERT2)1Soff/?	either: D2.Cg-Atf4<tm1.1Cmad> Tg(Myh11-icre/ERT2)1Soff or B6.Cg-Atf4<tm1.1Cmad> Tg(Myh11-icre/ERT2)1Soff	N	27812542
MGI:5812901	M	MP:0005376	homeostasis/metabolism phenotype	Gt(ROSA)26Sor<tm2(ATF4)Myz>/Gt(ROSA)26Sor<tm2(ATF4)Myz>,Tg(Myh11-icre/ERT2)1Soff/?	either: D2.Cg-Atf4<tm1.1Cmad> Tg(Myh11-icre/ERT2)1Soff or B6.Cg-Atf4<tm1.1Cmad> Tg(Myh11-icre/ERT2)1Soff	Y	27812542
MGI:5812912	M	MP:0001932	abnormal spermiogenesis	vtab/vtab	CBy.Cg-vtab/GrsrJ	N	MGI:5812893
MGI:5812912	M	MP:0002216	abnormal seminiferous tubule morphology	vtab/vtab	CBy.Cg-vtab/GrsrJ	N	MGI:5812893
MGI:5812912	M	MP:0004901	decreased male germ cell number	vtab/vtab	CBy.Cg-vtab/GrsrJ	N	MGI:5812893
MGI:5812912	M	MP:0001154	seminiferous tubule degeneration	vtab/vtab	CBy.Cg-vtab/GrsrJ	N	MGI:5812893
MGI:5812986	M	MP:0011964	increased total retina thickness	9930012K11Rik<tm2b(EUCOMM)Hmgu>/9930012K11Rik<tm2b(EUCOMM)Hmgu>	C57BL/6N-9930012K11Rik<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5812987	M	MP:0010024	increased total body fat amount	Abhd8<tm1b(EUCOMM)Wtsi>/Abhd8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abhd8<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5812987	F	MP:0003020	decreased circulating chloride level	Abhd8<tm1b(EUCOMM)Wtsi>/Abhd8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abhd8<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5812987	F	MP:0005179	decreased circulating cholesterol level	Abhd8<tm1b(EUCOMM)Wtsi>/Abhd8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abhd8<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5812987	F	MP:0005627	increased circulating potassium level	Abhd8<tm1b(EUCOMM)Wtsi>/Abhd8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abhd8<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5812987	F	MP:0000195	decreased circulating calcium level	Abhd8<tm1b(EUCOMM)Wtsi>/Abhd8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abhd8<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5812987	F	MP:0001258	decreased body length	Abhd8<tm1b(EUCOMM)Wtsi>/Abhd8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abhd8<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5812990	F	MP:0000691	enlarged spleen	Ascc2<tm1a(EUCOMM)Wtsi>/Ascc2<+>	C57BL/6N-Ascc2<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5812992	F	MP:0009263	abnormal eyelid fusion	Axin2<tm1b(KOMP)Wtsi>/Axin2<tm1b(KOMP)Wtsi>	C57BL/6N-Axin2<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5812992	M	MP:0001672	abnormal embryo development	Axin2<tm1b(KOMP)Wtsi>/Axin2<tm1b(KOMP)Wtsi>	C57BL/6N-Axin2<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5812992	F	MP:0009908	protruding tongue	Axin2<tm1b(KOMP)Wtsi>/Axin2<tm1b(KOMP)Wtsi>	C57BL/6N-Axin2<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5812994	F	MP:0001697	abnormal embryo size	Bcl7a<tm1b(EUCOMM)Wtsi>/Bcl7a<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bcl7a<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5812995	M	MP:0010025	decreased total body fat amount	Bhmt<tm1b(EUCOMM)Hmgu>/Bhmt<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bhmt<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5812995	F	MP:0002874	decreased hemoglobin content	Bhmt<tm1b(EUCOMM)Hmgu>/Bhmt<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bhmt<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5812995	M	MP:0003960	increased lean body mass	Bhmt<tm1b(EUCOMM)Hmgu>/Bhmt<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bhmt<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5812995	M	MP:0004952	increased spleen weight	Bhmt<tm1b(EUCOMM)Hmgu>/Bhmt<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bhmt<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5812995	F	MP:0005566	decreased blood urea nitrogen level	Bhmt<tm1b(EUCOMM)Hmgu>/Bhmt<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bhmt<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5812996	M	MP:0003960	increased lean body mass	Camk1<tm2b(EUCOMM)Hmgu>/Camk1<tm2b(EUCOMM)Hmgu>	C57BL/6N-Camk1<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5812996	M	MP:0002942	decreased circulating alanine transaminase level	Camk1<tm2b(EUCOMM)Hmgu>/Camk1<tm2b(EUCOMM)Hmgu>	C57BL/6N-Camk1<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5812996	M	MP:0000745	tremors	Camk1<tm2b(EUCOMM)Hmgu>/Camk1<tm2b(EUCOMM)Hmgu>	C57BL/6N-Camk1<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5812997	F	MP:0001926	female infertility	Ccnt2<tm1b(EUCOMM)Wtsi>/Ccnt2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ccnt2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5812997	M	MP:0001925	male infertility	Ccnt2<tm1b(EUCOMM)Wtsi>/Ccnt2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ccnt2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5812999	F	MP:0000689	abnormal spleen morphology	Cpne5<tm2b(EUCOMM)Hmgu>/Cpne5<tm2b(EUCOMM)Hmgu>	C57BL/6N-Cpne5<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813003	M	MP:0000689	abnormal spleen morphology	Eme1<tm1.1(KOMP)Wtsi>/Eme1<tm1.1(KOMP)Wtsi>	C57BL/6N-Eme1<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5813003	M	MP:0002608	increased hematocrit	Eme1<tm1.1(KOMP)Wtsi>/Eme1<tm1.1(KOMP)Wtsi>	C57BL/6N-Eme1<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5813004	F	MP:0002092	abnormal eye morphology	Eml2<tm1b(EUCOMM)Wtsi>/Eml2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eml2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5813004	M	MP:0002874	decreased hemoglobin content	Eml2<tm1b(EUCOMM)Wtsi>/Eml2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eml2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5813004	F	MP:0003731	abnormal retina outer nuclear layer morphology	Eml2<tm1b(EUCOMM)Wtsi>/Eml2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eml2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5813005	M	MP:0000691	enlarged spleen	Esyt2<tm2b(KOMP)Wtsi>/Esyt2<+>	C57BL/6N-Esyt2<tm2b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5813007	M	MP:0011239	abnormal skin coloration	Frmd4b<tm1b(EUCOMM)Wtsi>/Frmd4b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Frmd4b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5813007	F	MP:0002574	increased vertical activity	Frmd4b<tm1b(EUCOMM)Wtsi>/Frmd4b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Frmd4b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5813008	F	MP:0011239	abnormal skin coloration	Galntl5<tm1b(KOMP)Wtsi>/Galntl5<tm1b(KOMP)Wtsi>	C57BL/6N-Galntl5<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5813008	F	MP:0011959	abnormal eye posterior chamber depth	Galntl5<tm1b(KOMP)Wtsi>/Galntl5<tm1b(KOMP)Wtsi>	C57BL/6N-Galntl5<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5813010	F	MP:0000689	abnormal spleen morphology	Spmip2<tm1b(EUCOMM)Hmgu>/Spmip2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spmip2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813012	M	MP:0001510	abnormal coat appearance	Lamtor5<tm1b(EUCOMM)Hmgu>/Lamtor5<+>	C57BL/6N-Lamtor5<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813012	F	MP:0011239	abnormal skin coloration	Lamtor5<tm1b(EUCOMM)Hmgu>/Lamtor5<+>	C57BL/6N-Lamtor5<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813014	F	MP:0001325	abnormal retina morphology	Lrrc51<tm1b(EUCOMM)Hmgu>/Lrrc51<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lrrc51<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813014	M	MP:0010097	abnormal retina blood vessel morphology	Lrrc51<tm1b(EUCOMM)Hmgu>/Lrrc51<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lrrc51<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813014	F	MP:0011239	abnormal skin coloration	Lrrc51<tm1b(EUCOMM)Hmgu>/Lrrc51<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lrrc51<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813015	F	MP:0005419	decreased circulating serum albumin level	Mthfd1<tm2b(KOMP)Wtsi>/Mthfd1<+>	C57BL/6N-Mthfd1<tm2b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5813017	F	MP:0011110	preweaning lethality, incomplete penetrance	Muc5ac<tm2b(EUCOMM)Hmgu>/Muc5ac<tm2b(EUCOMM)Hmgu>	C57BL/6N-Muc5ac<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813019	M	MP:0004738	abnormal auditory brainstem response	Nin<tm1b(EUCOMM)Hmgu>/Nin<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nin<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5813019	M	MP:0009142	decreased prepulse inhibition	Nin<tm1b(EUCOMM)Hmgu>/Nin<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nin<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5813019	M	MP:0001489	decreased startle reflex	Nin<tm1b(EUCOMM)Hmgu>/Nin<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nin<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5813022	F	MP:0000689	abnormal spleen morphology	Pja2<tm1b(EUCOMM)Wtsi>/Pja2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pja2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5813022	M	MP:0002060	abnormal skin morphology	Pja2<tm1b(EUCOMM)Wtsi>/Pja2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pja2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5813027	F	MP:0000470	abnormal stomach morphology	Rufy3<tm1b(EUCOMM)Hmgu>/Rufy3<+>	C57BL/6N-Rufy3<tm1b(EUCOMM)Hmgu>/B08Rbrc	N	MGI:5576271
MGI:5813028	F	MP:0000063	decreased bone mineral density	Septin5<tm1b(EUCOMM)Hmgu>/Septin5<+>	C57BL/6N-Septin5<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5813028	F	MP:0000692	small spleen	Septin5<tm1b(EUCOMM)Hmgu>/Septin5<+>	C57BL/6N-Septin5<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5813028	F	MP:0003795	abnormal bone structure	Septin5<tm1b(EUCOMM)Hmgu>/Septin5<+>	C57BL/6N-Septin5<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5813028	F	MP:0010124	decreased bone mineral content	Septin5<tm1b(EUCOMM)Hmgu>/Septin5<+>	C57BL/6N-Septin5<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5813028	F	MP:0001258	decreased body length	Septin5<tm1b(EUCOMM)Hmgu>/Septin5<+>	C57BL/6N-Septin5<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:5813029	F	MP:0005293	impaired glucose tolerance	Sirpa<tm1b(EUCOMM)Hmgu>/Sirpa<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sirpa<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813029	F	MP:0005566	decreased blood urea nitrogen level	Sirpa<tm1b(EUCOMM)Hmgu>/Sirpa<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sirpa<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813030	M	MP:0001510	abnormal coat appearance	Slc44a1<tm1b(EUCOMM)Hmgu>/Slc44a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc44a1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813030	F	MP:0011959	abnormal eye posterior chamber depth	Slc44a1<tm1b(EUCOMM)Hmgu>/Slc44a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc44a1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813030	F	MP:0003731	abnormal retina outer nuclear layer morphology	Slc44a1<tm1b(EUCOMM)Hmgu>/Slc44a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc44a1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813030	F	MP:0011960	abnormal eye anterior chamber depth	Slc44a1<tm1b(EUCOMM)Hmgu>/Slc44a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc44a1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813030	F	MP:0001399	hyperactivity	Slc44a1<tm1b(EUCOMM)Hmgu>/Slc44a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc44a1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813030	M	MP:0002626	increased heart rate	Slc44a1<tm1b(EUCOMM)Hmgu>/Slc44a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc44a1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813030	M	MP:0010097	abnormal retina blood vessel morphology	Slc44a1<tm1b(EUCOMM)Hmgu>/Slc44a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc44a1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813030	F	MP:0011965	decreased total retina thickness	Slc44a1<tm1b(EUCOMM)Hmgu>/Slc44a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc44a1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813032	M	MP:0001289	persistence of hyaloid vascular system	Sox30<tm1b(KOMP)Wtsi>/Sox30<tm1b(KOMP)Wtsi>	C57BL/6N-Sox30<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5813032	F	MP:0003733	abnormal retina inner nuclear layer morphology	Sox30<tm1b(KOMP)Wtsi>/Sox30<tm1b(KOMP)Wtsi>	C57BL/6N-Sox30<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5813032	M	MP:0013279	increased fasting circulating glucose level	Sox30<tm1b(KOMP)Wtsi>/Sox30<tm1b(KOMP)Wtsi>	C57BL/6N-Sox30<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5813033	F	MP:0000063	decreased bone mineral density	Spidr<tm1b(EUCOMM)Hmgu>/Spidr<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spidr<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813033	F	MP:0001926	female infertility	Spidr<tm1b(EUCOMM)Hmgu>/Spidr<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spidr<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813033	F	MP:0010124	decreased bone mineral content	Spidr<tm1b(EUCOMM)Hmgu>/Spidr<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spidr<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813033	M	MP:0001925	male infertility	Spidr<tm1b(EUCOMM)Hmgu>/Spidr<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spidr<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813033	F	MP:0010024	increased total body fat amount	Spidr<tm1b(EUCOMM)Hmgu>/Spidr<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spidr<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813033	F	MP:0011959	abnormal eye posterior chamber depth	Spidr<tm1b(EUCOMM)Hmgu>/Spidr<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spidr<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813035	M	MP:0005419	decreased circulating serum albumin level	Taf6<tm1b(EUCOMM)Hmgu>/Taf6<+>	C57BL/6N-Taf6<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813035	M	MP:0011965	decreased total retina thickness	Taf6<tm1b(EUCOMM)Hmgu>/Taf6<+>	C57BL/6N-Taf6<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813035	F	MP:0005343	increased circulating aspartate transaminase level	Taf6<tm1b(EUCOMM)Hmgu>/Taf6<+>	C57BL/6N-Taf6<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813037	F	MP:0002135	abnormal kidney morphology	Tgm3<tm1b(KOMP)Wtsi>/Tgm3<tm1b(KOMP)Wtsi>	C57BL/6N-Tgm3<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5813038	M	MP:0001697	abnormal embryo size	Trib1<tm1b(KOMP)Wtsi>/Trib1<tm1b(KOMP)Wtsi>	C57BL/6N-Trib1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5813038	F	MP:0000063	decreased bone mineral density	Trib1<tm1b(KOMP)Wtsi>/Trib1<tm1b(KOMP)Wtsi>	C57BL/6N-Trib1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5813038	F	MP:0001510	abnormal coat appearance	Trib1<tm1b(KOMP)Wtsi>/Trib1<tm1b(KOMP)Wtsi>	C57BL/6N-Trib1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5813039	F	MP:0008806	increased circulating amylase level	Ube2j1<tm1.1(NCOM)Mfgc>/Ube2j1<tm1.1(NCOM)Mfgc>	C57BL/6N-Ube2j1<tm1.1(NCOM)Mfgc>/Rbrc	N	MGI:5576271
MGI:5813039	F	MP:0000063	decreased bone mineral density	Ube2j1<tm1.1(NCOM)Mfgc>/Ube2j1<tm1.1(NCOM)Mfgc>	C57BL/6N-Ube2j1<tm1.1(NCOM)Mfgc>/Rbrc	N	MGI:5576271
MGI:5813039	M	MP:0001925	male infertility	Ube2j1<tm1.1(NCOM)Mfgc>/Ube2j1<tm1.1(NCOM)Mfgc>	C57BL/6N-Ube2j1<tm1.1(NCOM)Mfgc>/Rbrc	N	MGI:5576271
MGI:5813039	M	MP:0002764	short tibia	Ube2j1<tm1.1(NCOM)Mfgc>/Ube2j1<tm1.1(NCOM)Mfgc>	C57BL/6N-Ube2j1<tm1.1(NCOM)Mfgc>/Rbrc	N	MGI:5576271
MGI:5813039	M	MP:0011941	increased fluid intake	Ube2j1<tm1.1(NCOM)Mfgc>/Ube2j1<tm1.1(NCOM)Mfgc>	C57BL/6N-Ube2j1<tm1.1(NCOM)Mfgc>/Rbrc	N	MGI:5576271
MGI:5813042	F	MP:0001399	hyperactivity	Zfp142<tm1b(EUCOMM)Wtsi>/Zfp142<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp142<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5813042	M	MP:0000689	abnormal spleen morphology	Zfp142<tm1b(EUCOMM)Wtsi>/Zfp142<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp142<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5813043	F	MP:0002135	abnormal kidney morphology	Zfp148<tm1b(EUCOMM)Hmgu>/Zfp148<+>	C57BL/6N-Zfp148<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813043	M	MP:0011239	abnormal skin coloration	Zfp148<tm1b(EUCOMM)Hmgu>/Zfp148<+>	C57BL/6N-Zfp148<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813043	F	MP:0000062	increased bone mineral density	Zfp148<tm1b(EUCOMM)Hmgu>/Zfp148<+>	C57BL/6N-Zfp148<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813044	F	MP:0001697	abnormal embryo size	Zfp148<tm1b(EUCOMM)Hmgu>/Zfp148<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp148<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5813045	M	MP:0001697	abnormal embryo size	Zfp609<tm1b(EUCOMM)Hmgu>/Zfp609<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp609<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5816266	F	MP:0002169	no abnormal phenotype detected	Syap1<tm1a(EUCOMM)Hmgu>/Syap1<tm1a(EUCOMM)Hmgu>	involves: C57BL/6J * C57BL/6N	N	27344443
MGI:5816267	M	MP:0002169	no abnormal phenotype detected	Syap1<tm1a(EUCOMM)Hmgu>/Y	involves: C57BL/6J * C57BL/6N	N	27344443
MGI:5816473	F	MP:0009363	abnormal tertiary ovarian follicle morphology	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0011124	increased primary ovarian follicle number	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0031020	premature ovarian failure	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0001130	abnormal ovarian folliculogenesis	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0001750	increased circulating follicle stimulating hormone level	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0001131	abnormal ovarian follicle morphology	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0004856	decreased ovary weight	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0001923	reduced female fertility	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0003953	abnormal hormone level	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0003696	abnormal zona pellucida morphology	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0002780	decreased circulating testosterone level	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0008871	abnormal ovarian follicle number	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0011129	decreased tertiary ovarian follicle number	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0001126	abnormal ovary morphology	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0002679	abnormal corpus luteum morphology	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0009433	polyovular ovarian follicle	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0008868	abnormal granulosa cell morphology	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0001926	female infertility	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816473	F	MP:0031420	decreased superovulation rate	C1galt1<tm1.1Rpmc>/C1galt1<tm1.1Rpmc>,Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Zp3-cre)1Gwh/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	21239444
MGI:5816488	M	MP:0009230	abnormal sperm head morphology	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	M	MP:0006380	abnormal spermatid morphology	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	M	MP:0002631	abnormal epididymis morphology	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	M	MP:0005159	azoospermia	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	M	MP:0001146	abnormal testis morphology	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	M	MP:0001932	abnormal spermiogenesis	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	F	MP:0005389	reproductive system phenotype	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	Y	26945718
MGI:5816488	M	MP:0009838	abnormal sperm axoneme morphology	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	M	MP:0008545	absent sperm flagellum	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	M	MP:0008898	abnormal acrosome morphology	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	M	MP:0009231	detached acrosome	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	M	MP:0004182	abnormal spermiation	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	M	MP:0001925	male infertility	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	M	MP:0009830	abnormal sperm connecting piece morphology	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	M	MP:0008892	abnormal sperm flagellum morphology	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816488	M	MP:0009232	abnormal sperm nucleus morphology	Ccdc42<tm1(KOMP)Vlcg>/Ccdc42<tm1(KOMP)Vlcg>	involves: C57BL/6J * C57BL/6NTac	N	26945718
MGI:5816712	M	MP:0002912	abnormal excitatory postsynaptic potential	Adk<tm2Bois>/Adk<tm2Bois>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27903722
MGI:5816712	M	MP:0002062	abnormal associative learning	Adk<tm2Bois>/Adk<tm2Bois>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27903722
MGI:5816712	M	MP:0009454	impaired contextual conditioning behavior	Adk<tm2Bois>/Adk<tm2Bois>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27903722
MGI:5816712	M	MP:0009358	environmentally induced seizures	Adk<tm2Bois>/Adk<tm2Bois>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27903722
MGI:5816712	M	MP:0004859	abnormal synaptic plasticity	Adk<tm2Bois>/Adk<tm2Bois>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27903722
MGI:5816712	M	MP:0002206	abnormal CNS synaptic transmission	Adk<tm2Bois>/Adk<tm2Bois>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27903722
MGI:5816712	M	MP:0002906	increased susceptibility to pharmacologically induced seizures	Adk<tm2Bois>/Adk<tm2Bois>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27903722
MGI:5816712	M	MP:0003008	enhanced long-term potentiation	Adk<tm2Bois>/Adk<tm2Bois>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27903722
MGI:5816712	M	MP:0000947	convulsive seizures	Adk<tm2Bois>/Adk<tm2Bois>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27903722
MGI:5816716	M	MP:0002083	premature death	Adk<tm2Bois>/Adk<tm2Bois>,Adora1<tm1Bbf>/Adora1<tm1Bbf>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	27903722
MGI:5816716	M	MP:0009358	environmentally induced seizures	Adk<tm2Bois>/Adk<tm2Bois>,Adora1<tm1Bbf>/Adora1<tm1Bbf>,Tg(Nes-cre)1Kln/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	27903722
MGI:5816717	M	MP:0012348	decreased susceptibility to induction of seizure by inducing agent	Adk<tm2Bois>/Adk<tm2Bois>,Adora2a<tm1Jfc>/Adora2a<tm1Jfc>,Tg(Nes-cre)1Kln/0	involves: 129S4/SvJae * C57BL/6 * SJL	N	27903722
MGI:5816717	M	MP:0005386	behavior/neurological phenotype	Adk<tm2Bois>/Adk<tm2Bois>,Adora2a<tm1Jfc>/Adora2a<tm1Jfc>,Tg(Nes-cre)1Kln/0	involves: 129S4/SvJae * C57BL/6 * SJL	Y	27903722
MGI:5816914	M	MP:0001409	increased stereotypic behavior	Shank2<tm1.1Bcgen>/Shank2<tm1.1Bcgen>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27903723
MGI:5816914	M	MP:0001405	impaired coordination	Shank2<tm1.1Bcgen>/Shank2<tm1.1Bcgen>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27903723
MGI:5816914	M	MP:0001363	increased anxiety-related response	Shank2<tm1.1Bcgen>/Shank2<tm1.1Bcgen>,Tg(Pcp2-cre)2Mpin/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27903723
MGI:5817399	M	MP:0009410	abnormal skeletal muscle satellite cell proliferation	Cd163<tm1(KOMP)Vlcg>/Cd163<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26242746
MGI:5817399	M	MP:0003060	increased aerobic running capacity	Cd163<tm1(KOMP)Vlcg>/Cd163<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26242746
MGI:5817399	M	MP:0010098	abnormal retina blood vessel pattern	Cd163<tm1(KOMP)Vlcg>/Cd163<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26242746
MGI:5817399	M	MP:0010210	abnormal circulating cytokine level	Cd163<tm1(KOMP)Vlcg>/Cd163<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26242746
MGI:5817399	M	MP:0010957	abnormal aerobic respiration	Cd163<tm1(KOMP)Vlcg>/Cd163<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26242746
MGI:5817399	M	MP:0031318	enhanced skeletal muscle regeneration	Cd163<tm1(KOMP)Vlcg>/Cd163<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26242746
MGI:5817399	M	MP:0003082	abnormal gastrocnemius morphology	Cd163<tm1(KOMP)Vlcg>/Cd163<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26242746
MGI:5817399	M	MP:0010760	abnormal macrophage chemotaxis	Cd163<tm1(KOMP)Vlcg>/Cd163<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	26242746
MGI:5817433	F	MP:0000493	rectal prolapse	Il10<tm1Cgn>/Il10<tm1Cgn>,Rreb1<Sao>/Rreb1<Sao>	NOD.Cg-Il10<tm1Cgn> Rreb1<Sao>	N	MGI:5817418
MGI:5817456	M	MP:0002687	oligozoospermia	Cfap54<Gt(IST10309B2)Tigm>/Cfap54<Gt(IST10309B2)Tigm>	(B6J.B6N-Cfap54<Gt(IST10309B2)Tigm> x 129S6.B6N-Cfap54<Gt(IST10309B2)Tigm>)F1	N	26224312
MGI:5817456	M	MP:0009239	short sperm flagellum	Cfap54<Gt(IST10309B2)Tigm>/Cfap54<Gt(IST10309B2)Tigm>	(B6J.B6N-Cfap54<Gt(IST10309B2)Tigm> x 129S6.B6N-Cfap54<Gt(IST10309B2)Tigm>)F1	N	26224312
MGI:5817456	M	MP:0009838	abnormal sperm axoneme morphology	Cfap54<Gt(IST10309B2)Tigm>/Cfap54<Gt(IST10309B2)Tigm>	(B6J.B6N-Cfap54<Gt(IST10309B2)Tigm> x 129S6.B6N-Cfap54<Gt(IST10309B2)Tigm>)F1	N	26224312
MGI:5817456	M	MP:0006380	abnormal spermatid morphology	Cfap54<Gt(IST10309B2)Tigm>/Cfap54<Gt(IST10309B2)Tigm>	(B6J.B6N-Cfap54<Gt(IST10309B2)Tigm> x 129S6.B6N-Cfap54<Gt(IST10309B2)Tigm>)F1	N	26224312
MGI:5817456	M	MP:0001932	abnormal spermiogenesis	Cfap54<Gt(IST10309B2)Tigm>/Cfap54<Gt(IST10309B2)Tigm>	(B6J.B6N-Cfap54<Gt(IST10309B2)Tigm> x 129S6.B6N-Cfap54<Gt(IST10309B2)Tigm>)F1	N	26224312
MGI:5817456	M	MP:0008545	absent sperm flagellum	Cfap54<Gt(IST10309B2)Tigm>/Cfap54<Gt(IST10309B2)Tigm>	(B6J.B6N-Cfap54<Gt(IST10309B2)Tigm> x 129S6.B6N-Cfap54<Gt(IST10309B2)Tigm>)F1	N	26224312
MGI:5817456	M	MP:0001925	male infertility	Cfap54<Gt(IST10309B2)Tigm>/Cfap54<Gt(IST10309B2)Tigm>	(B6J.B6N-Cfap54<Gt(IST10309B2)Tigm> x 129S6.B6N-Cfap54<Gt(IST10309B2)Tigm>)F1	N	26224312
MGI:5817471	M	MP:0002062	abnormal associative learning	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Nes-cre)1Kln/?	either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)	N	27693255
MGI:5817471	M	MP:0001405	impaired coordination	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Nes-cre)1Kln/?	either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)	N	27693255
MGI:5817471	M	MP:0009456	impaired cued conditioning behavior	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Nes-cre)1Kln/?	either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)	N	27693255
MGI:5817471	M	MP:0005386	behavior/neurological phenotype	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Nes-cre)1Kln/?	either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)	Y	27693255
MGI:5817471	F	MP:0001261	obese	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Nes-cre)1Kln/?	either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)	N	27693255
MGI:5817471	M	MP:0009454	impaired contextual conditioning behavior	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Nes-cre)1Kln/?	either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)	N	27693255
MGI:5817471	M	MP:0008428	abnormal spatial working memory	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Nes-cre)1Kln/?	either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)	N	27693255
MGI:5817608	M	MP:0001405	impaired coordination	Rai1<tm2.2Luo>/Rai1<+>,Tg(Nes-cre)1Kln/?	either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)	N	27693255
MGI:5817609	F	MP:0001261	obese	Rai1<tm2.1Luo>/Rai1<+>,Tg(Nes-cre)1Kln/?	either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)	N	27693255
MGI:5817609	M	MP:0001405	impaired coordination	Rai1<tm2.1Luo>/Rai1<+>,Tg(Nes-cre)1Kln/?	either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)	N	27693255
MGI:5817614	F	MP:0001261	obese	Rai1<tm2.2Luo>/Rai1<tm2.1Luo>,Tg(Nes-cre)1Kln/?	either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)	N	27693255
MGI:5817637	M	MP:0009454	impaired contextual conditioning behavior	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Slc17a6<tm2(cre)Lowl>/?	either: (involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6) or (involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	N	27693255
MGI:5817637	M	MP:0009456	impaired cued conditioning behavior	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Slc17a6<tm2(cre)Lowl>/?	either: (involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6) or (involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	N	27693255
MGI:5817637	M	MP:0001405	impaired coordination	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Slc17a6<tm2(cre)Lowl>/?	either: (involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6) or (involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	N	27693255
MGI:5817637	M	MP:0002062	abnormal associative learning	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Slc17a6<tm2(cre)Lowl>/?	either: (involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6) or (involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	N	27693255
MGI:5817641	M	MP:0001405	impaired coordination	Rai1<tm2.1Luo>/Rai1<+>,Slc17a6<tm2(cre)Lowl>/?	either: (involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6) or (involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	N	27693255
MGI:5817645	M	MP:0009454	impaired contextual conditioning behavior	Gad2<tm2(cre)Zjh>/?,Rai1<tm2.1Luo>/Rai1<tm2.1Luo>	either: (involves: 129S1/Sv * 129S4/SvJae * C57BL/6) or (involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6)	N	27693255
MGI:5817645	M	MP:0002062	abnormal associative learning	Gad2<tm2(cre)Zjh>/?,Rai1<tm2.1Luo>/Rai1<tm2.1Luo>	either: (involves: 129S1/Sv * 129S4/SvJae * C57BL/6) or (involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6)	N	27693255
MGI:5817645	M	MP:0009456	impaired cued conditioning behavior	Gad2<tm2(cre)Zjh>/?,Rai1<tm2.1Luo>/Rai1<tm2.1Luo>	either: (involves: 129S1/Sv * 129S4/SvJae * C57BL/6) or (involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6)	N	27693255
MGI:5817650	F	MP:0001261	obese	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Sim1-cre)1Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817650	M	MP:0001402	decreased locomotor activity	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Sim1-cre)1Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817650	F	MP:0000182	increased circulating LDL cholesterol level	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Sim1-cre)1Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817650	F	MP:0001433	polyphagia	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Sim1-cre)1Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817650	F	MP:0014142	increased body fat mass	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Sim1-cre)1Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817650	F	MP:0005145	increased circulating VLDL cholesterol level	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Sim1-cre)1Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817650	F	MP:0001556	increased circulating HDL cholesterol level	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Sim1-cre)1Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817650	M	MP:0005386	behavior/neurological phenotype	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Sim1-cre)1Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	Y	27693255
MGI:5817650	F	MP:0003982	increased cholesterol level	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Sim1-cre)1Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817650	F	MP:0005317	increased triglyceride level	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Sim1-cre)1Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817650	F	MP:0008908	increased total fat pad weight	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Sim1-cre)1Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817650	F	MP:0003960	increased lean body mass	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Sim1-cre)1Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817653	F	MP:0001260	increased body weight	Rai1<tm2.1Luo>/Rai1<+>,Tg(Sim1-cre)1Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817657	F	MP:0001260	increased body weight	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Nr5a1-cre)7Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817657	M	MP:0005386	behavior/neurological phenotype	Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Nr5a1-cre)7Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	Y	27693255
MGI:5817661	F	MP:0001260	increased body weight	Rai1<tm2.1Luo>/Rai1<+>,Tg(Nr5a1-cre)7Lowl/?	either: (involves: 129S1/Sv * C57BL/6 * FVB) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)	N	27693255
MGI:5817765	F	MP:0001931	abnormal oogenesis	Sohlh1<tm1Rajk>/Sohlh1<tm1Rajk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	N	16690745
MGI:5817765	F	MP:0004805	absent oocytes	Sohlh1<tm1Rajk>/Sohlh1<tm1Rajk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	N	16690745
MGI:5817765	F	MP:0011126	absent primary ovarian follicles	Sohlh1<tm1Rajk>/Sohlh1<tm1Rajk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	N	16690745
MGI:5817765	F	MP:0002777	absent ovarian follicles	Sohlh1<tm1Rajk>/Sohlh1<tm1Rajk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	N	16690745
MGI:5817765	F	MP:0005431	decreased oocyte number	Sohlh1<tm1Rajk>/Sohlh1<tm1Rajk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	N	16690745
MGI:5817765	F	MP:0004833	ovary atrophy	Sohlh1<tm1Rajk>/Sohlh1<tm1Rajk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	N	16690745
MGI:5817765	F	MP:0001926	female infertility	Sohlh1<tm1Rajk>/Sohlh1<tm1Rajk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	N	16690745
MGI:5817765	F	MP:0001129	impaired ovarian folliculogenesis	Sohlh1<tm1Rajk>/Sohlh1<tm1Rajk>	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	N	16690745
MGI:5817790	M	MP:0000281	abnormal interventricular septum morphology	Scube3<m1Mhda>/Scube3<m1Mhda>	C3HeB/FeJ-Scube3<m1Mhda>	N	27815347
MGI:5817790	M	MP:0003916	decreased heart left ventricle weight	Scube3<m1Mhda>/Scube3<m1Mhda>	C3HeB/FeJ-Scube3<m1Mhda>	N	27815347
MGI:5817790	M	MP:0005179	decreased circulating cholesterol level	Scube3<m1Mhda>/Scube3<m1Mhda>	C3HeB/FeJ-Scube3<m1Mhda>	N	27815347
MGI:5817790	M	MP:0000198	decreased circulating phosphate level	Scube3<m1Mhda>/Scube3<m1Mhda>	C3HeB/FeJ-Scube3<m1Mhda>	N	27815347
MGI:5817790	M	MP:0005567	decreased circulating total protein level	Scube3<m1Mhda>/Scube3<m1Mhda>	C3HeB/FeJ-Scube3<m1Mhda>	N	27815347
MGI:5817790	F	MP:0000194	increased circulating calcium level	Scube3<m1Mhda>/Scube3<m1Mhda>	C3HeB/FeJ-Scube3<m1Mhda>	N	27815347
MGI:5817790	M	MP:0010392	prolonged QRS complex duration	Scube3<m1Mhda>/Scube3<m1Mhda>	C3HeB/FeJ-Scube3<m1Mhda>	N	27815347
MGI:5817790	F	MP:0005574	decreased pulmonary respiratory rate	Scube3<m1Mhda>/Scube3<m1Mhda>	C3HeB/FeJ-Scube3<m1Mhda>	N	27815347
MGI:5817790	M	MP:0005419	decreased circulating serum albumin level	Scube3<m1Mhda>/Scube3<m1Mhda>	C3HeB/FeJ-Scube3<m1Mhda>	N	27815347
MGI:5817790	M	MP:0014316	decreased heart left ventricle posterior wall thickness	Scube3<m1Mhda>/Scube3<m1Mhda>	C3HeB/FeJ-Scube3<m1Mhda>	N	27815347
MGI:5817988	F	MP:0012411	increased granulosa cell tumor incidence	Bap1<em2Test>/Bap1<+>	involves: FVB	N	26896281
MGI:5817988	F	MP:0008000	increased ovary tumor incidence	Bap1<em2Test>/Bap1<+>	involves: FVB	N	26896281
MGI:5817989	F	MP:0012411	increased granulosa cell tumor incidence	Bap1<em3Test>/Bap1<+>	involves: FVB	N	26896281
MGI:5817989	F	MP:0008000	increased ovary tumor incidence	Bap1<em3Test>/Bap1<+>	involves: FVB	N	26896281
MGI:5817994	F	MP:0008805	decreased circulating amylase level	Wbp2<tm2a(EUCOMM)Wtsi>/Wbp2<tm2a(EUCOMM)Wtsi>	involves: C57BL/6N * C57BL/6NTac	N	26881968
MGI:5818291	M	MP:0012336	decreased vitamin D level	Gnas<tm5.1Lsw>/Gnas<tm5.1Lsw>,Tg(Slc5a2-cre)1Tauc/0	involves: C57BL/6 * DBA/2	N	26671181
MGI:5819194	M	MP:0005169	abnormal male meiosis	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0005159	azoospermia	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0001156	abnormal spermatogenesis	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0013601	increased testis apoptosis	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0006378	abnormal spermatogonia morphology	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0009452	abnormal synaptonemal complex	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0010207	abnormal telomere morphology	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0006380	abnormal spermatid morphology	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0001147	small testis	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0004852	decreased testis weight	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0001940	testis hypoplasia	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0001925	male infertility	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0004025	polyploidy	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0001153	small seminiferous tubules	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0006379	abnormal spermatocyte morphology	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0010948	abnormal double-strand DNA break repair	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	M	MP:0003830	abnormal testis development	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819194	F	MP:0005431	decreased oocyte number	Cep63<Gt(EUCE0251h11)Hmgu>/Cep63<Gt(EUCE0251h11)Hmgu>	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	N	26158450
MGI:5819222	M	MP:0010614	abnormal mitral valve cusp morphology	Tns1<tm1Efu>/Tns1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ	N	26301497
MGI:5819222	M	MP:0000286	abnormal mitral valve morphology	Tns1<tm1Efu>/Tns1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ	N	26301497
MGI:5822918	M	MP:0010398	decreased liver glycogen level	Blvra<tm1c(EUCOMM)Hmgu>/Blvra<tm1c(EUCOMM)Hmgu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6J * C57BL/6N	N	27738106
MGI:5822918	M	MP:0002079	increased circulating insulin level	Blvra<tm1c(EUCOMM)Hmgu>/Blvra<tm1c(EUCOMM)Hmgu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6J * C57BL/6N	N	27738106
MGI:5822918	M	MP:0013279	increased fasting circulating glucose level	Blvra<tm1c(EUCOMM)Hmgu>/Blvra<tm1c(EUCOMM)Hmgu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6J * C57BL/6N	N	27738106
MGI:5822918	M	MP:0002628	hepatic steatosis	Blvra<tm1c(EUCOMM)Hmgu>/Blvra<tm1c(EUCOMM)Hmgu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6J * C57BL/6N	N	27738106
MGI:5822918	M	MP:0005293	impaired glucose tolerance	Blvra<tm1c(EUCOMM)Hmgu>/Blvra<tm1c(EUCOMM)Hmgu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6J * C57BL/6N	N	27738106
MGI:5822918	M	MP:0014174	decreased fatty acid beta-oxidation	Blvra<tm1c(EUCOMM)Hmgu>/Blvra<tm1c(EUCOMM)Hmgu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6J * C57BL/6N	N	27738106
MGI:5822918	M	MP:0005331	insulin resistance	Blvra<tm1c(EUCOMM)Hmgu>/Blvra<tm1c(EUCOMM)Hmgu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6J * C57BL/6N	N	27738106
MGI:5822918	M	MP:0005281	increased fatty acids level	Blvra<tm1c(EUCOMM)Hmgu>/Blvra<tm1c(EUCOMM)Hmgu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6J * C57BL/6N	N	27738106
MGI:5822918	M	MP:0009355	increased liver triglyceride level	Blvra<tm1c(EUCOMM)Hmgu>/Blvra<tm1c(EUCOMM)Hmgu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6J * C57BL/6N	N	27738106
MGI:5823026	F	MP:0001613	abnormal vasodilation	Ido1<tm1.1Mkks>/Ido1<tm1.1Mkks>	B6.Cg-Ido1<tm1.1Mkks>	N	25602015
MGI:5823026	F	MP:0009661	abnormal pregnancy	Ido1<tm1.1Mkks>/Ido1<tm1.1Mkks>	B6.Cg-Ido1<tm1.1Mkks>	N	25602015
MGI:5823026	F	MP:0002962	increased urine protein level	Ido1<tm1.1Mkks>/Ido1<tm1.1Mkks>	B6.Cg-Ido1<tm1.1Mkks>	N	25602015
MGI:5823026	F	MP:0003699	abnormal female reproductive system physiology	Ido1<tm1.1Mkks>/Ido1<tm1.1Mkks>	B6.Cg-Ido1<tm1.1Mkks>	N	25602015
MGI:5823026	F	MP:0002842	increased systemic arterial blood pressure	Ido1<tm1.1Mkks>/Ido1<tm1.1Mkks>	B6.Cg-Ido1<tm1.1Mkks>	N	25602015
MGI:5823026	F	MP:0005333	decreased heart rate	Ido1<tm1.1Mkks>/Ido1<tm1.1Mkks>	B6.Cg-Ido1<tm1.1Mkks>	N	25602015
MGI:5823026	F	MP:0005325	abnormal renal glomerulus morphology	Ido1<tm1.1Mkks>/Ido1<tm1.1Mkks>	B6.Cg-Ido1<tm1.1Mkks>	N	25602015
MGI:5823060	F	MP:0011913	abnormal reticulocyte cell number	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	27666489
MGI:5823060	M	MP:0002875	decreased erythrocyte cell number	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	27666489
MGI:5823060	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	27666489
MGI:5823060	F	MP:0002875	decreased erythrocyte cell number	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	27666489
MGI:5823060	F	MP:0003135	increased erythroid progenitor cell number	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	27666489
MGI:5823404	M	MP:0003917	increased kidney weight	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823404	M	MP:0011435	increased urine magnesium level	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823404	M	MP:0009810	increased urine uric acid level	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823404	M	MP:0002901	increased urine phosphate level	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823404	M	MP:0003068	enlarged kidney	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823404	M	MP:0002135	abnormal kidney morphology	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823404	M	MP:0000521	abnormal kidney cortex morphology	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823404	M	MP:0031003	increased kidney glycogen level	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823404	M	MP:0009643	abnormal urine homeostasis	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823404	M	MP:0002959	increased urine microalbumin level	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823404	M	MP:0005326	abnormal podocyte morphology	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823404	M	MP:0002703	abnormal renal tubule morphology	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823404	M	MP:0009350	decreased urine pH	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823404	M	MP:0008821	increased blood uric acid level	G6pc1<tm1.1Ics>/G6pc1<tm1.1Ics>,Tg(Kap-icre)29066/2Sig/0	involves: 129S2/SvPas * C57BL/6J * SJL	N	24717294
MGI:5823987	F	MP:0001131	abnormal ovarian follicle morphology	Tmco1<em1Smoc>/Tmco1<em1Smoc>	C57BL/6J-Tmco1<em1Smoc>	N	29467381
MGI:5824058	M	MP:0009356	decreased liver triglyceride level	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0005179	decreased circulating cholesterol level	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0005292	improved glucose tolerance	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0003799	impaired macrophage chemotaxis	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0013278	decreased fasting circulating glucose level	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0003383	abnormal gluconeogenesis	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0005560	decreased circulating glucose level	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0008114	abnormal Kupffer cell morphology	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0009133	decreased white fat cell size	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0005584	abnormal enzyme/coenzyme activity	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0002891	increased insulin sensitivity	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0010182	decreased susceptibility to weight gain	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0011940	decreased food intake	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0005289	increased oxygen consumption	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0002727	decreased circulating insulin level	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824058	M	MP:0010379	decreased respiratory quotient	Foxo6<tm1(KOMP)Vlcg>/Foxo6<tm1(KOMP)Vlcg>	B6J.B6NTac-Foxo6<tm1(KOMP)Vlcg>	N	25944898
MGI:5824119	M	MP:0001360	abnormal social investigation	Tsc2<tm1Djk>/Tsc2<+>	involves: 129S4/SvJae * C57BL/6J	N	25155956
MGI:5824119	M	MP:0008260	abnormal autophagy	Tsc2<tm1Djk>/Tsc2<+>	involves: 129S4/SvJae * C57BL/6J	N	25155956
MGI:5824119	M	MP:0003461	abnormal response to novel object	Tsc2<tm1Djk>/Tsc2<+>	involves: 129S4/SvJae * C57BL/6J	N	25155956
MGI:5824119	M	MP:0020395	abnormal response to social novelty	Tsc2<tm1Djk>/Tsc2<+>	involves: 129S4/SvJae * C57BL/6J	N	25155956
MGI:5824119	M	MP:0009936	abnormal dendritic spine morphology	Tsc2<tm1Djk>/Tsc2<+>	involves: 129S4/SvJae * C57BL/6J	N	25155956
MGI:5824247	F	MP:0009505	abnormal mammary gland lobule morphology	Tg(Erbb2-Erbb2)NN60Led/0	involves: FVB/N	N	10803404
MGI:5824247	F	MP:0000627	abnormal mammary gland morphology	Tg(Erbb2-Erbb2)NN60Led/0	involves: FVB/N	N	10803404
MGI:5824247	F	MP:0009503	abnormal mammary gland duct morphology	Tg(Erbb2-Erbb2)NN60Led/0	involves: FVB/N	N	10803404
MGI:5824247	F	MP:0001884	mammary gland alveolar hyperplasia	Tg(Erbb2-Erbb2)NN60Led/0	involves: FVB/N	N	10803404
MGI:5824247	F	MP:0013488	increased keratoacanthoma incidence	Tg(Erbb2-Erbb2)NN60Led/0	involves: FVB/N	N	10803404
MGI:5824247	F	MP:0006271	abnormal involution of the mammary gland	Tg(Erbb2-Erbb2)NN60Led/0	involves: FVB/N	N	10803404
MGI:5824247	F	MP:0001882	abnormal lactation	Tg(Erbb2-Erbb2)NN60Led/0	involves: FVB/N	N	10803404
MGI:5824254	F	MP:0006271	abnormal involution of the mammary gland	Tg(Erbb2-Erbb2*V664E)#Led/0	involves: FVB/N	N	10803404
MGI:5824254	F	MP:0001883	increased mammary adenocarcinoma incidence	Tg(Erbb2-Erbb2*V664E)#Led/0	involves: FVB/N	N	10803404
MGI:5824254	F	MP:0000630	mammary gland hyperplasia	Tg(Erbb2-Erbb2*V664E)#Led/0	involves: FVB/N	N	10803404
MGI:5824254	F	MP:0001882	abnormal lactation	Tg(Erbb2-Erbb2*V664E)#Led/0	involves: FVB/N	N	10803404
MGI:5824254	F	MP:0001881	abnormal mammary gland physiology	Tg(Erbb2-Erbb2*V664E)#Led/0	involves: FVB/N	N	10803404
MGI:5824254	F	MP:0009505	abnormal mammary gland lobule morphology	Tg(Erbb2-Erbb2*V664E)#Led/0	involves: FVB/N	N	10803404
MGI:5824254	F	MP:0012570	increased mammary gland tumor incidence in breeding females	Tg(Erbb2-Erbb2*V664E)#Led/0	involves: FVB/N	N	10803404
MGI:5824293	M	MP:0005342	abnormal intestinal lipid absorption	Tm6sf2<tm1a(KOMP)Wtsi>/Tm6sf2<tm1a(KOMP)Wtsi>	C57BL/6N-Tm6sf2<tm1a(KOMP)Wtsi>	N	27013658
MGI:5824293	M	MP:0000183	decreased circulating LDL cholesterol level	Tm6sf2<tm1a(KOMP)Wtsi>/Tm6sf2<tm1a(KOMP)Wtsi>	C57BL/6N-Tm6sf2<tm1a(KOMP)Wtsi>	N	27013658
MGI:5824293	M	MP:0005179	decreased circulating cholesterol level	Tm6sf2<tm1a(KOMP)Wtsi>/Tm6sf2<tm1a(KOMP)Wtsi>	C57BL/6N-Tm6sf2<tm1a(KOMP)Wtsi>	N	27013658
MGI:5824293	M	MP:0002941	increased circulating alanine transaminase level	Tm6sf2<tm1a(KOMP)Wtsi>/Tm6sf2<tm1a(KOMP)Wtsi>	C57BL/6N-Tm6sf2<tm1a(KOMP)Wtsi>	N	27013658
MGI:5824293	M	MP:0000186	decreased circulating HDL cholesterol level	Tm6sf2<tm1a(KOMP)Wtsi>/Tm6sf2<tm1a(KOMP)Wtsi>	C57BL/6N-Tm6sf2<tm1a(KOMP)Wtsi>	N	27013658
MGI:5824293	M	MP:0001552	increased circulating triglyceride level	Tm6sf2<tm1a(KOMP)Wtsi>/Tm6sf2<tm1a(KOMP)Wtsi>	C57BL/6N-Tm6sf2<tm1a(KOMP)Wtsi>	N	27013658
MGI:5824293	M	MP:0003976	decreased circulating VLDL triglyceride level	Tm6sf2<tm1a(KOMP)Wtsi>/Tm6sf2<tm1a(KOMP)Wtsi>	C57BL/6N-Tm6sf2<tm1a(KOMP)Wtsi>	N	27013658
MGI:5824293	M	MP:0005317	increased triglyceride level	Tm6sf2<tm1a(KOMP)Wtsi>/Tm6sf2<tm1a(KOMP)Wtsi>	C57BL/6N-Tm6sf2<tm1a(KOMP)Wtsi>	N	27013658
MGI:5824293	M	MP:0010332	abnormal circulating apolipoprotein level	Tm6sf2<tm1a(KOMP)Wtsi>/Tm6sf2<tm1a(KOMP)Wtsi>	C57BL/6N-Tm6sf2<tm1a(KOMP)Wtsi>	N	27013658
MGI:5824293	M	MP:0002647	decreased intestinal cholesterol absorption	Tm6sf2<tm1a(KOMP)Wtsi>/Tm6sf2<tm1a(KOMP)Wtsi>	C57BL/6N-Tm6sf2<tm1a(KOMP)Wtsi>	N	27013658
MGI:5824293	M	MP:0000479	abnormal enterocyte morphology	Tm6sf2<tm1a(KOMP)Wtsi>/Tm6sf2<tm1a(KOMP)Wtsi>	C57BL/6N-Tm6sf2<tm1a(KOMP)Wtsi>	N	27013658
MGI:5824296	M	MP:0009355	increased liver triglyceride level	Tm6sf2<tm1a(KOMP)Wtsi>/Tm6sf2<+>	C57BL/6N-Tm6sf2<tm1a(KOMP)Wtsi>	N	27013658
MGI:5824296	M	MP:0005278	abnormal cholesterol homeostasis	Tm6sf2<tm1a(KOMP)Wtsi>/Tm6sf2<+>	C57BL/6N-Tm6sf2<tm1a(KOMP)Wtsi>	N	27013658
MGI:5824730	M	MP:0003989	abnormal barrel cortex morphology	Dlg3<tm1Grnt>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	27466188
MGI:5824730	M	MP:0005404	abnormal axon morphology	Dlg3<tm1Grnt>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	27466188
MGI:5824730	M	MP:0020066	abnormal neocortex size	Dlg3<tm1Grnt>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	27466188
MGI:5824730	M	MP:0002184	abnormal innervation	Dlg3<tm1Grnt>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	27466188
MGI:5824730	M	MP:0002152	abnormal brain morphology	Dlg3<tm1Grnt>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	27466188
MGI:5824730	M	MP:0009538	abnormal synapse morphology	Dlg3<tm1Grnt>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	27466188
MGI:5824730	M	MP:0011270	decreased excitatory postsynaptic current amplitude	Dlg3<tm1Grnt>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	27466188
MGI:5824730	M	MP:0000859	abnormal somatosensory cortex morphology	Dlg3<tm1Grnt>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	27466188
MGI:5824730	M	MP:0011273	prolonged excitatory postsynaptic current decay time	Dlg3<tm1Grnt>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	27466188
MGI:5825021	M	MP:0008414	abnormal spatial reference memory	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6N	N	25485098
MGI:5825021	M	MP:0012307	impaired spatial learning	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6N	N	25485098
MGI:5825021	M	MP:0001402	decreased locomotor activity	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6N	N	25485098
MGI:5825021	M	MP:0001458	abnormal object recognition memory	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6N	N	25485098
MGI:5825021	M	MP:0010065	decreased circulating creatine level	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6N	N	25485098
MGI:5825021	M	MP:0001262	decreased body weight	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6N	N	25485098
MGI:5825021	M	MP:0010062	decreased creatine level	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6N	N	25485098
MGI:5825021	M	MP:0001522	impaired swimming	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6N	N	25485098
MGI:5825021	M	MP:0030633	decreased urine creatine level	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6N	N	25485098
MGI:5825021	M	MP:0008428	abnormal spatial working memory	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6N	N	25485098
MGI:5825026	M	MP:0014365	impaired short-term object recognition memory	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0008842	lipofuscinosis	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0001441	increased grooming behavior	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0010062	decreased creatine level	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0001262	decreased body weight	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0020083	decreased hippocampus volume	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0008428	abnormal spatial working memory	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0001405	impaired coordination	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0003245	abnormal GABAergic neuron morphology	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0009967	abnormal neuron proliferation	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0008414	abnormal spatial reference memory	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0000812	abnormal dentate gyrus morphology	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0008918	microgliosis	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0001458	abnormal object recognition memory	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0009538	abnormal synapse morphology	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825026	M	MP:0014367	impaired long-term object recognition memory	Slc6a8<tm1.2Lbar>/Y	involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	N	27466184
MGI:5825029	M	MP:0001458	abnormal object recognition memory	Slc6a8<tm1.1Lbar>/Y,Tg(Nes-cre)1Kln/0	involves: 129 * C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	27466184
MGI:5825029	M	MP:0010062	decreased creatine level	Slc6a8<tm1.1Lbar>/Y,Tg(Nes-cre)1Kln/0	involves: 129 * C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	27466184
MGI:5825029	M	MP:0014367	impaired long-term object recognition memory	Slc6a8<tm1.1Lbar>/Y,Tg(Nes-cre)1Kln/0	involves: 129 * C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	27466184
MGI:5825029	M	MP:0000812	abnormal dentate gyrus morphology	Slc6a8<tm1.1Lbar>/Y,Tg(Nes-cre)1Kln/0	involves: 129 * C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	27466184
MGI:5825029	M	MP:0014365	impaired short-term object recognition memory	Slc6a8<tm1.1Lbar>/Y,Tg(Nes-cre)1Kln/0	involves: 129 * C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	27466184
MGI:5825029	M	MP:0008428	abnormal spatial working memory	Slc6a8<tm1.1Lbar>/Y,Tg(Nes-cre)1Kln/0	involves: 129 * C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	27466184
MGI:5825029	M	MP:0009967	abnormal neuron proliferation	Slc6a8<tm1.1Lbar>/Y,Tg(Nes-cre)1Kln/0	involves: 129 * C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	27466184
MGI:5825177	F	MP:0000133	abnormal long bone metaphysis morphology	Spp1<tm1.1Dhd>/Spp1<tm1.1Dhd>	involves: 129P2/OlaHsd * C57BL/6	N	18050311
MGI:5825475	M	MP:0002216	abnormal seminiferous tubule morphology	Tafazzin<tm1Dost>/Y	involves: 129P2/OlaHsd	N	26114544
MGI:5825475	M	MP:0005159	azoospermia	Tafazzin<tm1Dost>/Y	involves: 129P2/OlaHsd	N	26114544
MGI:5825475	M	MP:0001925	male infertility	Tafazzin<tm1Dost>/Y	involves: 129P2/OlaHsd	N	26114544
MGI:5825475	M	MP:0006379	abnormal spermatocyte morphology	Tafazzin<tm1Dost>/Y	involves: 129P2/OlaHsd	N	26114544
MGI:5825475	M	MP:0001146	abnormal testis morphology	Tafazzin<tm1Dost>/Y	involves: 129P2/OlaHsd	N	26114544
MGI:5825475	M	MP:0005169	abnormal male meiosis	Tafazzin<tm1Dost>/Y	involves: 129P2/OlaHsd	N	26114544
MGI:5825475	M	MP:0001147	small testis	Tafazzin<tm1Dost>/Y	involves: 129P2/OlaHsd	N	26114544
MGI:5825475	M	MP:0005385	cardiovascular system phenotype	Tafazzin<tm1Dost>/Y	involves: 129P2/OlaHsd	Y	26114544
MGI:5827756	F	MP:0000630	mammary gland hyperplasia	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-Kras2)12Hev/0	involves: FVB/N	N	18356293
MGI:5827756	F	MP:0010299	increased mammary gland tumor incidence	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-Kras2)12Hev/0	involves: FVB/N	N	18356293
MGI:5827758	F	MP:0010299	increased mammary gland tumor incidence	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-Kras2)12Hev/0,Tg(tetO-MYC)1Lach/0	involves: FVB/N	N	18356293
MGI:5827758	F	MP:0000630	mammary gland hyperplasia	Tg(MMTV-rtTA)1Lach/0,Tg(tetO-Kras2)12Hev/0,Tg(tetO-MYC)1Lach/0	involves: FVB/N	N	18356293
MGI:5827760	F	MP:0010299	increased mammary gland tumor incidence	Tg(MMTV-Myc)141-3Led/0,Tg(MMTV-rtTA)1Lach/0,Tg(tetO-Kras2)12Hev/0	involves: C57BL/6J * CD-1 * FVB/N	N	18356293
MGI:5827826	M	MP:0002727	decreased circulating insulin level	Draxin<tm1Lex>/Draxin<tm1Lex>	B6;129S5-Draxin<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5827834	M	MP:0010166	increased response to stress-induced hyperthermia	Emc7<tm1Lex>/Emc7<+>	B6;129S5-Emc7<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5827837	M	MP:0002644	decreased circulating triglyceride level	Snorc<tm1Lex>/Snorc<tm1Lex>	B6;129S5-Snorc<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5827837	F	MP:0001402	decreased locomotor activity	Snorc<tm1Lex>/Snorc<tm1Lex>	B6;129S5-Snorc<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5827844	M	MP:0005385	cardiovascular system phenotype	Smad1<tm1Rjle>/Smad1<+>	involves: 129S6/SvEvTac * C57BL/6	Y	26076038
MGI:5827848	M	MP:0000276	heart right ventricle hypertrophy	Bmpr2<tm1Mmue>/Bmpr2<+>,Smad1<tm1Rjle>/Smad1<+>	involves: 129S1/SvImJ * 129S6/SvEvTac * C57BL/6	N	26076038
MGI:5827848	M	MP:0010758	increased right ventricle systolic pressure	Bmpr2<tm1Mmue>/Bmpr2<+>,Smad1<tm1Rjle>/Smad1<+>	involves: 129S1/SvImJ * 129S6/SvEvTac * C57BL/6	N	26076038
MGI:5827854	M	MP:0001925	male infertility	Elapor1<tm1Lex>/Elapor1<tm1Lex>	B6;129S5-Elapor1<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5827855	M	MP:0005178	increased circulating cholesterol level	Cacfd1<tm1Lex>/Cacfd1<tm1Lex>	B6;129S5-Cacfd1<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5827985	F	MP:0001973	increased thermal nociceptive threshold	9430015G10Rik<tm1Lex>/9430015G10Rik<tm1Lex>	B6;129S5-9430015G10Rik<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5827987	M	MP:0002635	reduced sensorimotor gating	Atp13a5<tm1Lex>/Atp13a5<tm1Lex>	B6;129S5-Atp13a5<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5828132	M	MP:0001364	decreased anxiety-related response	Chst14<tm1Lex>/Chst14<tm1Lex>	B6;129S5-Chst14<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5828156	M	MP:0005293	impaired glucose tolerance	Scn2b<tm1Lex>/Scn2b<tm1Lex>	B6;129S5-Scn2b<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5828261	M	MP:0005508	abnormal skeleton morphology	Crispld2<tm1Lex>/Crispld2<tm1Lex>	B6;129S5-Crispld2<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5828261	M	MP:0005292	improved glucose tolerance	Crispld2<tm1Lex>/Crispld2<tm1Lex>	B6;129S5-Crispld2<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5828264	F	MP:0001861	lung inflammation	Ace2<tm1Lex>/Ace2<tm1Lex>	B6;129S5-Ace2<tm1Lex>/Mmucd	N	27019629
MGI:5828264	F	MP:0003184	increased angiotensin I-converting enzyme activity	Ace2<tm1Lex>/Ace2<tm1Lex>	B6;129S5-Ace2<tm1Lex>/Mmucd	N	27019629
MGI:5828264	F	MP:0005573	increased pulmonary respiratory rate	Ace2<tm1Lex>/Ace2<tm1Lex>	B6;129S5-Ace2<tm1Lex>/Mmucd	N	27019629
MGI:5828264	F	MP:0003136	yellow coat color	Ace2<tm1Lex>/Ace2<tm1Lex>	B6;129S5-Ace2<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5828264	F	MP:0005584	abnormal enzyme/coenzyme activity	Ace2<tm1Lex>/Ace2<tm1Lex>	B6;129S5-Ace2<tm1Lex>/Mmucd	N	27019629
MGI:5828265	M	MP:0003136	yellow coat color	Ace2<tm1Lex>/Y	B6;129S5-Ace2<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5828413	F	MP:0012322	decreased total tissue mass	Dnajc10<tm1Lex>/Dnajc10<tm1Lex>	B6;129S5-Dnajc10<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5828413	F	MP:0001258	decreased body length	Dnajc10<tm1Lex>/Dnajc10<tm1Lex>	B6;129S5-Dnajc10<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5828413	F	MP:0001262	decreased body weight	Dnajc10<tm1Lex>/Dnajc10<tm1Lex>	B6;129S5-Dnajc10<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5828413	F	MP:0003961	decreased lean body mass	Dnajc10<tm1Lex>/Dnajc10<tm1Lex>	B6;129S5-Dnajc10<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5828515	M	MP:0002781	increased circulating testosterone level	Tg(SHBG)4-aGlha/0	involves: C57BL/6 * CBA	N	9440816
MGI:5828522	F	MP:0002016	ovary cyst	Ntmt1<tm1(NCOM)Mfgc>/Ntmt1<tm1(NCOM)Mfgc>	involves: C57BL/6J * C57BL/6NCrl	N	25843235
MGI:5828522	M	MP:0003786	premature aging	Ntmt1<tm1(NCOM)Mfgc>/Ntmt1<tm1(NCOM)Mfgc>	involves: C57BL/6J * C57BL/6NCrl	N	25843235
MGI:5828522	M	MP:0005114	premature hair loss	Ntmt1<tm1(NCOM)Mfgc>/Ntmt1<tm1(NCOM)Mfgc>	involves: C57BL/6J * C57BL/6NCrl	N	25843235
MGI:5828522	F	MP:0008869	anovulation	Ntmt1<tm1(NCOM)Mfgc>/Ntmt1<tm1(NCOM)Mfgc>	involves: C57BL/6J * C57BL/6NCrl	N	25843235
MGI:5828522	F	MP:0001127	small ovary	Ntmt1<tm1(NCOM)Mfgc>/Ntmt1<tm1(NCOM)Mfgc>	involves: C57BL/6J * C57BL/6NCrl	N	25843235
MGI:5828522	F	MP:0001134	absent corpus luteum	Ntmt1<tm1(NCOM)Mfgc>/Ntmt1<tm1(NCOM)Mfgc>	involves: C57BL/6J * C57BL/6NCrl	N	25843235
MGI:5828522	F	MP:0001926	female infertility	Ntmt1<tm1(NCOM)Mfgc>/Ntmt1<tm1(NCOM)Mfgc>	involves: C57BL/6J * C57BL/6NCrl	N	25843235
MGI:5828522	M	MP:0005389	reproductive system phenotype	Ntmt1<tm1(NCOM)Mfgc>/Ntmt1<tm1(NCOM)Mfgc>	involves: C57BL/6J * C57BL/6NCrl	Y	25843235
MGI:5828524	M	MP:0002781	increased circulating testosterone level	Lepr<db>/Lepr<db>,Tg(SHBG)4-aGlha/0	involves: C57BL/6 * C57BLKS/J * CBA	N	26441241
MGI:5828524	M	MP:0009642	abnormal blood homeostasis	Lepr<db>/Lepr<db>,Tg(SHBG)4-aGlha/0	involves: C57BL/6 * C57BLKS/J * CBA	N	26441241
MGI:5829181	M	MP:0002635	reduced sensorimotor gating	Glt8d1<tm1Lex>/Glt8d1<tm1Lex>	B6;129S5-Glt8d1<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5829191	F	MP:0011806	decreased dermal fibroblast proliferation	Alg2<tm1Lex>/Alg2<+>	B6;129S5-Alg2<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5829198	M	MP:0001222	epidermal hyperplasia	Gpx8<tm1Lex>/Gpx8<tm1Lex>	B6;129S5-Gpx8<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5829198	M	MP:0001194	dermatitis	Gpx8<tm1Lex>/Gpx8<tm1Lex>	B6;129S5-Gpx8<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5829198	M	MP:0001242	hyperkeratosis	Gpx8<tm1Lex>/Gpx8<tm1Lex>	B6;129S5-Gpx8<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5829219	F	MP:0005333	decreased heart rate	Lyzl1<tm1Lex>/Lyzl1<tm1Lex>	B6;129S5-Lyzl1<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5829229	M	MP:0001175	abnormal lung morphology	Setd7<tm1.1Ital>/Setd7<tm1.1Ital>	involves: C57BL/6 * CBA	N	27292644
MGI:5829229	M	MP:0013258	abnormal extracellular matrix morphology	Setd7<tm1.1Ital>/Setd7<tm1.1Ital>	involves: C57BL/6 * CBA	N	27292644
MGI:5829229	M	MP:0005166	decreased susceptibility to injury	Setd7<tm1.1Ital>/Setd7<tm1.1Ital>	involves: C57BL/6 * CBA	N	27292644
MGI:5829229	M	MP:0002333	abnormal lung compliance	Setd7<tm1.1Ital>/Setd7<tm1.1Ital>	involves: C57BL/6 * CBA	N	27292644
MGI:5829229	M	MP:0008469	abnormal protein level	Setd7<tm1.1Ital>/Setd7<tm1.1Ital>	involves: C57BL/6 * CBA	N	27292644
MGI:5829229	M	MP:0008874	decreased physiological sensitivity to xenobiotic	Setd7<tm1.1Ital>/Setd7<tm1.1Ital>	involves: C57BL/6 * CBA	N	27292644
MGI:5829230	M	MP:0005293	impaired glucose tolerance	Glb1l2<tm1Lex>/Glb1l2<tm1Lex>	B6;129S5-Glb1l2<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5829262	F	MP:0001264	increased body size	Fcrl2<tm1Lex>/Fcrl2<tm1Lex>	B6;129S5-Fcrl2<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5829262	F	MP:0010024	increased total body fat amount	Fcrl2<tm1Lex>/Fcrl2<tm1Lex>	B6;129S5-Fcrl2<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5829262	F	MP:0003960	increased lean body mass	Fcrl2<tm1Lex>/Fcrl2<tm1Lex>	B6;129S5-Fcrl2<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5829262	F	MP:0012323	increased total tissue mass	Fcrl2<tm1Lex>/Fcrl2<tm1Lex>	B6;129S5-Fcrl2<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5829262	F	MP:0001260	increased body weight	Fcrl2<tm1Lex>/Fcrl2<tm1Lex>	B6;129S5-Fcrl2<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5829405	M	MP:0008539	decreased susceptibility to induced colitis	Muc4<tm1Skb>/Muc4<tm1Skb>	involves: 129 * C57BL/6J	N	26364605
MGI:5829405	M	MP:0013299	decreased susceptibility to colitis induced morbidity/mortality	Muc4<tm1Skb>/Muc4<tm1Skb>	involves: 129 * C57BL/6J	N	26364605
MGI:5881975	F	MP:0002773	decreased circulating luteinizing hormone level	Lep<tm1.1Gvcao>/Lep<tm1.1Gvcao>,Tg(Adipoq-cre)1Evdr/0	involves: 129S4/SvJaeSor * C57BL/6J * FVB/NTac	N	25116704
MGI:5881975	M	MP:0003973	increased pituitary hormone level	Lep<tm1.1Gvcao>/Lep<tm1.1Gvcao>,Tg(Adipoq-cre)1Evdr/0	involves: 129S4/SvJaeSor * C57BL/6J * FVB/NTac	N	25116704
MGI:5881975	M	MP:0005120	decreased circulating growth hormone level	Lep<tm1.1Gvcao>/Lep<tm1.1Gvcao>,Tg(Adipoq-cre)1Evdr/0	involves: 129S4/SvJaeSor * C57BL/6J * FVB/NTac	N	25116704
MGI:5881975	F	MP:0005121	decreased circulating prolactin level	Lep<tm1.1Gvcao>/Lep<tm1.1Gvcao>,Tg(Adipoq-cre)1Evdr/0	involves: 129S4/SvJaeSor * C57BL/6J * FVB/NTac	N	25116704
MGI:5881975	F	MP:0001926	female infertility	Lep<tm1.1Gvcao>/Lep<tm1.1Gvcao>,Tg(Adipoq-cre)1Evdr/0	involves: 129S4/SvJaeSor * C57BL/6J * FVB/NTac	N	25116704
MGI:5881975	M	MP:0002790	decreased circulating follicle stimulating hormone level	Lep<tm1.1Gvcao>/Lep<tm1.1Gvcao>,Tg(Adipoq-cre)1Evdr/0	involves: 129S4/SvJaeSor * C57BL/6J * FVB/NTac	N	25116704
MGI:5881975	M	MP:0001925	male infertility	Lep<tm1.1Gvcao>/Lep<tm1.1Gvcao>,Tg(Adipoq-cre)1Evdr/0	involves: 129S4/SvJaeSor * C57BL/6J * FVB/NTac	N	25116704
MGI:5881977	F	MP:0005121	decreased circulating prolactin level	Lep<tm1.2Gvcao>/Lep<tm1.2Gvcao>	involves: 129S4/SvJaeSor * FVB/NJ * FVB/NTac	N	25116704
MGI:5881977	F	MP:0001926	female infertility	Lep<tm1.2Gvcao>/Lep<tm1.2Gvcao>	involves: 129S4/SvJaeSor * FVB/NJ * FVB/NTac	N	25116704
MGI:5881977	M	MP:0001925	male infertility	Lep<tm1.2Gvcao>/Lep<tm1.2Gvcao>	involves: 129S4/SvJaeSor * FVB/NJ * FVB/NTac	N	25116704
MGI:5881977	M	MP:0002790	decreased circulating follicle stimulating hormone level	Lep<tm1.2Gvcao>/Lep<tm1.2Gvcao>	involves: 129S4/SvJaeSor * FVB/NJ * FVB/NTac	N	25116704
MGI:5882203	M	MP:0001925	male infertility	Hsd17b14<tm1Lex>/Hsd17b14<tm1Lex>	B6;129S5-Hsd17b14<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5882203	M	MP:0010166	increased response to stress-induced hyperthermia	Hsd17b14<tm1Lex>/Hsd17b14<tm1Lex>	B6;129S5-Hsd17b14<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5882203	M	MP:0013600	testis degeneration	Hsd17b14<tm1Lex>/Hsd17b14<tm1Lex>	B6;129S5-Hsd17b14<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5882203	M	MP:0002687	oligozoospermia	Hsd17b14<tm1Lex>/Hsd17b14<tm1Lex>	B6;129S5-Hsd17b14<tm1Lex>/Mmucd	N	MGI:5000289
MGI:5882334	M	MP:0001258	decreased body length	Ppargc1a<tm1Aztc>/Ppargc1a<+>	C57BL/6-Ppargc1a<tm1Aztc>	N	MGI:2655403
MGI:5882334	M	MP:0003961	decreased lean body mass	Ppargc1a<tm1Aztc>/Ppargc1a<+>	C57BL/6-Ppargc1a<tm1Aztc>	N	MGI:2655403
MGI:5882334	M	MP:0010124	decreased bone mineral content	Ppargc1a<tm1Aztc>/Ppargc1a<+>	C57BL/6-Ppargc1a<tm1Aztc>	N	MGI:2655403
MGI:5882334	M	MP:0001262	decreased body weight	Ppargc1a<tm1Aztc>/Ppargc1a<+>	C57BL/6-Ppargc1a<tm1Aztc>	N	MGI:2655403
MGI:5882338	F	MP:0002727	decreased circulating insulin level	Ppargc1a<tm1Aztc>/Ppargc1a<tm1Aztc>	C57BL/6-Ppargc1a<tm1Aztc>	N	MGI:2655403
MGI:5882338	F	MP:0014143	decreased body fat mass	Ppargc1a<tm1Aztc>/Ppargc1a<tm1Aztc>	C57BL/6-Ppargc1a<tm1Aztc>	N	MGI:2655403
MGI:5882338	F	MP:0005560	decreased circulating glucose level	Ppargc1a<tm1Aztc>/Ppargc1a<tm1Aztc>	C57BL/6-Ppargc1a<tm1Aztc>	N	MGI:2655403
MGI:5882338	F	MP:0003961	decreased lean body mass	Ppargc1a<tm1Aztc>/Ppargc1a<tm1Aztc>	C57BL/6-Ppargc1a<tm1Aztc>	N	MGI:2655403
MGI:5882338	F	MP:0001262	decreased body weight	Ppargc1a<tm1Aztc>/Ppargc1a<tm1Aztc>	C57BL/6-Ppargc1a<tm1Aztc>	N	MGI:2655403
MGI:5882393	M	MP:0005389	reproductive system phenotype	Wbp2nl<tm1.1Osb>/Wbp2nl<tm1.1Osb>	involves: C57BL/6N * C57BL/6NCr * DBA/2	Y	26377222
MGI:5883575	M	MP:0003059	decreased insulin secretion	Senp1<tm1.1Eyeh>/Senp1<tm1.1Eyeh>	Not Specified	N	26389676
MGI:5883575	M	MP:0003562	abnormal pancreatic beta cell physiology	Senp1<tm1.1Eyeh>/Senp1<tm1.1Eyeh>	Not Specified	N	26389676
MGI:5883576	M	MP:0003059	decreased insulin secretion	Senp1<tm1.1Eyeh>/Senp1<tm1.1Eyeh>,Tg(Pdx1-cre)6Tuv/0	involves: C57BL/6	N	26389676
MGI:5883576	M	MP:0003562	abnormal pancreatic beta cell physiology	Senp1<tm1.1Eyeh>/Senp1<tm1.1Eyeh>,Tg(Pdx1-cre)6Tuv/0	involves: C57BL/6	N	26389676
MGI:5883576	M	MP:0002578	impaired ability to fire action potentials	Senp1<tm1.1Eyeh>/Senp1<tm1.1Eyeh>,Tg(Pdx1-cre)6Tuv/0	involves: C57BL/6	N	26389676
MGI:5883576	M	MP:0002727	decreased circulating insulin level	Senp1<tm1.1Eyeh>/Senp1<tm1.1Eyeh>,Tg(Pdx1-cre)6Tuv/0	involves: C57BL/6	N	26389676
MGI:5883576	M	MP:0005293	impaired glucose tolerance	Senp1<tm1.1Eyeh>/Senp1<tm1.1Eyeh>,Tg(Pdx1-cre)6Tuv/0	involves: C57BL/6	N	26389676
MGI:5883576	M	MP:0005378	growth/size/body region phenotype	Senp1<tm1.1Eyeh>/Senp1<tm1.1Eyeh>,Tg(Pdx1-cre)6Tuv/0	involves: C57BL/6	Y	26389676
MGI:5883577	M	MP:0005293	impaired glucose tolerance	Senp1<tm1.1Eyeh>/Senp1<+>,Tg(Pdx1-cre)6Tuv/0	involves: C57BL/6	N	26389676
MGI:5883578	M	MP:0003059	decreased insulin secretion	Senp1<tm1.1Eyeh>/Senp1<tm1.1Eyeh>,Tg(Pdx1-cre/Esr1*)#Dam/0	involves: C57BL/6	N	26389676
MGI:5883578	M	MP:0005293	impaired glucose tolerance	Senp1<tm1.1Eyeh>/Senp1<tm1.1Eyeh>,Tg(Pdx1-cre/Esr1*)#Dam/0	involves: C57BL/6	N	26389676
MGI:5883624	F	MP:0001926	female infertility	Esr2<tm1.1Gust>/Esr2<tm1.1Gust>	B6J.129X1(Cg)-Esr2<tm1.1Gust>	N	25848008
MGI:5883624	F	MP:0001132	absent mature ovarian follicles	Esr2<tm1.1Gust>/Esr2<tm1.1Gust>	B6J.129X1(Cg)-Esr2<tm1.1Gust>	N	25848008
MGI:5883624	F	MP:0009363	abnormal tertiary ovarian follicle morphology	Esr2<tm1.1Gust>/Esr2<tm1.1Gust>	B6J.129X1(Cg)-Esr2<tm1.1Gust>	N	25848008
MGI:5883624	F	MP:0031239	increased atretic ovarian follicle number	Esr2<tm1.1Gust>/Esr2<tm1.1Gust>	B6J.129X1(Cg)-Esr2<tm1.1Gust>	N	25848008
MGI:5883624	F	MP:0001134	absent corpus luteum	Esr2<tm1.1Gust>/Esr2<tm1.1Gust>	B6J.129X1(Cg)-Esr2<tm1.1Gust>	N	25848008
MGI:5883624	F	MP:0008869	anovulation	Esr2<tm1.1Gust>/Esr2<tm1.1Gust>	B6J.129X1(Cg)-Esr2<tm1.1Gust>	N	25848008
MGI:5883624	M	MP:0005389	reproductive system phenotype	Esr2<tm1.1Gust>/Esr2<tm1.1Gust>	B6J.129X1(Cg)-Esr2<tm1.1Gust>	Y	25848008
MGI:5883624	F	MP:0031383	increased secondary ovarian follicle number	Esr2<tm1.1Gust>/Esr2<tm1.1Gust>	B6J.129X1(Cg)-Esr2<tm1.1Gust>	N	25848008
MGI:5883628	M	MP:0004994	abnormal brain wave pattern	Kdm1a<tm1Ebg>/Kdm1a<tm1Ebg>	B6.129-Kdm1a<tm1Ebg>	N	24735673
MGI:5883628	M	MP:0003997	tonic-clonic seizures	Kdm1a<tm1Ebg>/Kdm1a<tm1Ebg>	B6.129-Kdm1a<tm1Ebg>	N	24735673
MGI:5883628	M	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality	Kdm1a<tm1Ebg>/Kdm1a<tm1Ebg>	B6.129-Kdm1a<tm1Ebg>	N	24735673
MGI:5883628	M	MP:0002887	decreased susceptibility to pharmacologically induced seizures	Kdm1a<tm1Ebg>/Kdm1a<tm1Ebg>	B6.129-Kdm1a<tm1Ebg>	N	24735673
MGI:5883628	M	MP:0003631	nervous system phenotype	Kdm1a<tm1Ebg>/Kdm1a<tm1Ebg>	B6.129-Kdm1a<tm1Ebg>	Y	24735673
MGI:5883628	M	MP:0003216	absence seizures	Kdm1a<tm1Ebg>/Kdm1a<tm1Ebg>	B6.129-Kdm1a<tm1Ebg>	N	24735673
MGI:5883880	M	MP:0010025	decreased total body fat amount	Gas2l2<tm1a(KOMP)Wtsi>/Gas2l2<tm1a(KOMP)Wtsi>	C57BL/6N-Gas2l2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5883880	F	MP:0001926	female infertility	Gas2l2<tm1a(KOMP)Wtsi>/Gas2l2<tm1a(KOMP)Wtsi>	C57BL/6N-Gas2l2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5883880	M	MP:0006358	absent pinna reflex	Gas2l2<tm1a(KOMP)Wtsi>/Gas2l2<tm1a(KOMP)Wtsi>	C57BL/6N-Gas2l2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5883880	M	MP:0001925	male infertility	Gas2l2<tm1a(KOMP)Wtsi>/Gas2l2<tm1a(KOMP)Wtsi>	C57BL/6N-Gas2l2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5883888	M	MP:0010052	increased grip strength	Unk<tm1a(KOMP)Wtsi>/Unk<tm1a(KOMP)Wtsi>	C57BL/6N-Unk<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5883888	F	MP:0001258	decreased body length	Unk<tm1a(KOMP)Wtsi>/Unk<tm1a(KOMP)Wtsi>	C57BL/6N-Unk<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:5883974	M	MP:0003020	decreased circulating chloride level	Adad1<em1(IMPC)J>/Adad1<+>	C57BL/6NJ-Adad1<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883974	F	MP:0004151	decreased circulating iron level	Adad1<em1(IMPC)J>/Adad1<+>	C57BL/6NJ-Adad1<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883976	F	MP:0001926	female infertility	Adad2<em1(IMPC)J>/Adad2<em1(IMPC)J>	C57BL/6NJ-Adad2<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883976	M	MP:0001925	male infertility	Adad2<em1(IMPC)J>/Adad2<em1(IMPC)J>	C57BL/6NJ-Adad2<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883976	M	MP:0003064	decreased coping response	Adad2<em1(IMPC)J>/Adad2<em1(IMPC)J>	C57BL/6NJ-Adad2<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883978	F	MP:0000274	enlarged heart	Akap10<tm1.1(KOMP)Vlcg>/Akap10<+>	C57BL/6N-Akap10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883978	F	MP:0000266	abnormal heart morphology	Akap10<tm1.1(KOMP)Vlcg>/Akap10<+>	C57BL/6N-Akap10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883979	M	MP:0008528	polycystic kidney	Arih2<tm1.1(KOMP)Vlcg>/Arih2<+>	C57BL/6N-Arih2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883979	F	MP:0001697	abnormal embryo size	Arih2<tm1.1(KOMP)Vlcg>/Arih2<+>	C57BL/6N-Arih2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883979	F	MP:0002060	abnormal skin morphology	Arih2<tm1.1(KOMP)Vlcg>/Arih2<+>	C57BL/6N-Arih2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883979	M	MP:0011625	cystolithiasis	Arih2<tm1.1(KOMP)Vlcg>/Arih2<+>	C57BL/6N-Arih2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883979	M	MP:0002135	abnormal kidney morphology	Arih2<tm1.1(KOMP)Vlcg>/Arih2<+>	C57BL/6N-Arih2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883979	F	MP:0003984	embryonic growth retardation	Arih2<tm1.1(KOMP)Vlcg>/Arih2<+>	C57BL/6N-Arih2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883979	M	MP:0000274	enlarged heart	Arih2<tm1.1(KOMP)Vlcg>/Arih2<+>	C57BL/6N-Arih2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883979	M	MP:0000266	abnormal heart morphology	Arih2<tm1.1(KOMP)Vlcg>/Arih2<+>	C57BL/6N-Arih2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883979	M	MP:0000538	abnormal urinary bladder morphology	Arih2<tm1.1(KOMP)Vlcg>/Arih2<+>	C57BL/6N-Arih2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883981	M	MP:0000219	increased neutrophil cell number	Timd6<tm1b(KOMP)Wtsi>/Timd6<+>	C57BL/6N-Timd6<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5883981	M	MP:0001512	trunk curl	Timd6<tm1b(KOMP)Wtsi>/Timd6<+>	C57BL/6N-Timd6<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5883981	M	MP:0005016	decreased lymphocyte cell number	Timd6<tm1b(KOMP)Wtsi>/Timd6<+>	C57BL/6N-Timd6<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5883981	M	MP:0004952	increased spleen weight	Timd6<tm1b(KOMP)Wtsi>/Timd6<+>	C57BL/6N-Timd6<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:5883982	F	MP:0011436	decreased urine magnesium level	Bmp2k<em1(IMPC)J>/Bmp2k<em1(IMPC)J>	C57BL/6NJ-Bmp2k<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883982	F	MP:0001303	abnormal lens morphology	Bmp2k<em1(IMPC)J>/Bmp2k<em1(IMPC)J>	C57BL/6NJ-Bmp2k<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883983	F	MP:0002968	increased circulating alkaline phosphatase level	Chn1<em1(IMPC)J>/Chn1<+>	C57BL/6NJ-Chn1<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883987	F	MP:0008528	polycystic kidney	Dnal1<tm1.1(KOMP)Vlcg>/Dnal1<+>	C57BL/6N-Dnal1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883987	F	MP:0002581	abnormal ileum morphology	Dnal1<tm1.1(KOMP)Vlcg>/Dnal1<+>	C57BL/6N-Dnal1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883987	M	MP:0001175	abnormal lung morphology	Dnal1<tm1.1(KOMP)Vlcg>/Dnal1<+>	C57BL/6N-Dnal1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883987	F	MP:0010378	increased respiratory quotient	Dnal1<tm1.1(KOMP)Vlcg>/Dnal1<+>	C57BL/6N-Dnal1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883987	M	MP:0005012	decreased eosinophil cell number	Dnal1<tm1.1(KOMP)Vlcg>/Dnal1<+>	C57BL/6N-Dnal1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883991	F	MP:0001102	small superior vagus ganglion	Emc6<tm1.1(KOMP)Vlcg>/Emc6<+>	C57BL/6N-Emc6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883991	F	MP:0009709	hydrometra	Emc6<tm1.1(KOMP)Vlcg>/Emc6<+>	C57BL/6N-Emc6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883991	F	MP:0002608	increased hematocrit	Emc6<tm1.1(KOMP)Vlcg>/Emc6<+>	C57BL/6N-Emc6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883992	M	MP:0001523	impaired righting response	Eogt<em1(IMPC)J>/Eogt<em1(IMPC)J>	C57BL/6NJ-Eogt<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883993	M	MP:0005633	increased circulating sodium level	Exoc4<em1(IMPC)J>/Exoc4<+>	C57BL/6NJ-Exoc4<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883996	F	MP:0011396	abnormal sleep behavior	Fastkd5<em1(IMPC)J>/Fastkd5<em1(IMPC)J>	C57BL/6NJ-Fastkd5<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883996	M	MP:0005560	decreased circulating glucose level	Fastkd5<em1(IMPC)J>/Fastkd5<em1(IMPC)J>	C57BL/6NJ-Fastkd5<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883996	M	MP:0001523	impaired righting response	Fastkd5<em1(IMPC)J>/Fastkd5<em1(IMPC)J>	C57BL/6NJ-Fastkd5<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883996	F	MP:0010393	shortened QRS complex duration	Fastkd5<em1(IMPC)J>/Fastkd5<em1(IMPC)J>	C57BL/6NJ-Fastkd5<em1(IMPC)J>/J	N	MGI:5576271
MGI:5883997	F	MP:0020870	decreased thigmotaxis	Fscn1<tm1.1(KOMP)Vlcg>/Fscn1<+>	C57BL/6N-Fscn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5883997	F	MP:0004924	abnormal behavior	Fscn1<tm1.1(KOMP)Vlcg>/Fscn1<+>	C57BL/6N-Fscn1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0002989	small kidney	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	F	MP:0001126	abnormal ovary morphology	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	F	MP:0003578	absent ovary	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0001925	male infertility	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0003918	decreased kidney weight	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0001262	decreased body weight	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0006415	absent testes	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0001146	abnormal testis morphology	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0005553	increased circulating creatinine level	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0002059	abnormal seminal vesicle morphology	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0002135	abnormal kidney morphology	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	F	MP:0001402	decreased locomotor activity	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	F	MP:0003558	absent uterus	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0004727	absent epididymis	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0002834	decreased heart weight	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	F	MP:0001926	female infertility	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0002631	abnormal epididymis morphology	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	F	MP:0003795	abnormal bone structure	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0004952	increased spleen weight	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0003402	decreased liver weight	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	F	MP:0001120	abnormal uterus morphology	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884003	M	MP:0003642	absent seminal vesicle	Kiss1r<tm1.1(KOMP)Vlcg>/Kiss1r<tm1.1(KOMP)Vlcg>	C57BL/6N-Kiss1r<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884005	F	MP:0005343	increased circulating aspartate transaminase level	Lum<tm1.1(KOMP)Vlcg>/Lum<+>	C57BL/6N-Lum<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884005	F	MP:0002941	increased circulating alanine transaminase level	Lum<tm1.1(KOMP)Vlcg>/Lum<+>	C57BL/6N-Lum<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5884006	F	MP:0001303	abnormal lens morphology	Med20<em1(IMPC)J>/Med20<+>	C57BL/6NJ-Med20<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884006	F	MP:0000221	decreased leukocyte cell number	Med20<em1(IMPC)J>/Med20<+>	C57BL/6NJ-Med20<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884008	F	MP:0002792	abnormal retina vasculature morphology	Mpdz<em1(IMPC)J>/Mpdz<em1(IMPC)J>	C57BL/6NJ-Mpdz<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884008	M	MP:0002833	increased heart weight	Mpdz<em1(IMPC)J>/Mpdz<em1(IMPC)J>	C57BL/6NJ-Mpdz<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884008	M	MP:0005292	improved glucose tolerance	Mpdz<em1(IMPC)J>/Mpdz<em1(IMPC)J>	C57BL/6NJ-Mpdz<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884008	F	MP:0010053	decreased grip strength	Mpdz<em1(IMPC)J>/Mpdz<em1(IMPC)J>	C57BL/6NJ-Mpdz<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884012	F	MP:0013279	increased fasting circulating glucose level	Myh10<em1(IMPC)J>/Myh10<+>	C57BL/6NJ-Myh10<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884013	F	MP:0001785	edema	Myh10<em1(IMPC)J>/Myh10<em1(IMPC)J>	C57BL/6NJ-Myh10<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884013	F	MP:0004258	abnormal placenta size	Myh10<em1(IMPC)J>/Myh10<em1(IMPC)J>	C57BL/6NJ-Myh10<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884013	F	MP:0011239	abnormal skin coloration	Myh10<em1(IMPC)J>/Myh10<em1(IMPC)J>	C57BL/6NJ-Myh10<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884014	F	MP:0001325	abnormal retina morphology	Ncoa6<em1(IMPC)J>/Ncoa6<+>	C57BL/6NJ-Ncoa6<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884016	F	MP:0002874	decreased hemoglobin content	Ndufs7<tm1b(EUCOMM)Hmgu>/Ndufs7<+>	C57BL/6N-Ndufs7<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5884016	M	MP:0011965	decreased total retina thickness	Ndufs7<tm1b(EUCOMM)Hmgu>/Ndufs7<+>	C57BL/6N-Ndufs7<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5884018	M	MP:0008797	facial cleft	Nxn<em1(IMPC)J>/Nxn<em1(IMPC)J>	C57BL/6NJ-Nxn<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884019	F	MP:0005140	decreased cardiac muscle contractility	Nxn<tm1a(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5884019	F	MP:0001293	anophthalmia	Nxn<tm1a(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5884019	F	MP:0001319	irregularly shaped pupil	Nxn<tm1a(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5884024	M	MP:0010379	decreased respiratory quotient	Prdm14<tm1a(EUCOMM)Wtsi>/Prdm14<tm1a(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5884024	M	MP:0001399	hyperactivity	Prdm14<tm1a(EUCOMM)Wtsi>/Prdm14<tm1a(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5884024	F	MP:0010024	increased total body fat amount	Prdm14<tm1a(EUCOMM)Wtsi>/Prdm14<tm1a(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5884024	M	MP:0001925	male infertility	Prdm14<tm1a(EUCOMM)Wtsi>/Prdm14<tm1a(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5884024	F	MP:0000063	decreased bone mineral density	Prdm14<tm1a(EUCOMM)Wtsi>/Prdm14<tm1a(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5884024	F	MP:0003795	abnormal bone structure	Prdm14<tm1a(EUCOMM)Wtsi>/Prdm14<tm1a(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5884024	F	MP:0010124	decreased bone mineral content	Prdm14<tm1a(EUCOMM)Wtsi>/Prdm14<tm1a(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5884024	F	MP:0005293	impaired glucose tolerance	Prdm14<tm1a(EUCOMM)Wtsi>/Prdm14<tm1a(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5884024	M	MP:0013772	increased effector memory T-helper cell number	Prdm14<tm1a(EUCOMM)Wtsi>/Prdm14<tm1a(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5884024	F	MP:0003961	decreased lean body mass	Prdm14<tm1a(EUCOMM)Wtsi>/Prdm14<tm1a(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1a(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5884025	F	MP:0000221	decreased leukocyte cell number	Prss56<em1(IMPC)J>/Prss56<em1(IMPC)J>	C57BL/6NJ-Prss56<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884026	F	MP:0005344	increased circulating bilirubin level	Riok2<tm1b(KOMP)Wtsi>/Riok2<+>	C57BL/6N-Riok2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5884026	M	MP:0000274	enlarged heart	Riok2<tm1b(KOMP)Wtsi>/Riok2<+>	C57BL/6N-Riok2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5884026	F	MP:0002941	increased circulating alanine transaminase level	Riok2<tm1b(KOMP)Wtsi>/Riok2<+>	C57BL/6N-Riok2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5884026	F	MP:0005343	increased circulating aspartate transaminase level	Riok2<tm1b(KOMP)Wtsi>/Riok2<+>	C57BL/6N-Riok2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:5884027	F	MP:0005565	increased blood urea nitrogen level	Sgsh<em3(IMPC)Tcp>/Sgsh<em3(IMPC)Tcp>	C57BL/6NCrl-Sgsh<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:5884027	F	MP:0002968	increased circulating alkaline phosphatase level	Sgsh<em3(IMPC)Tcp>/Sgsh<em3(IMPC)Tcp>	C57BL/6NCrl-Sgsh<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:5884027	M	MP:0001488	increased startle reflex	Sgsh<em3(IMPC)Tcp>/Sgsh<em3(IMPC)Tcp>	C57BL/6NCrl-Sgsh<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:5884027	M	MP:0010123	increased bone mineral content	Sgsh<em3(IMPC)Tcp>/Sgsh<em3(IMPC)Tcp>	C57BL/6NCrl-Sgsh<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:5884027	M	MP:0010025	decreased total body fat amount	Sgsh<em3(IMPC)Tcp>/Sgsh<em3(IMPC)Tcp>	C57BL/6NCrl-Sgsh<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:5884027	M	MP:0000062	increased bone mineral density	Sgsh<em3(IMPC)Tcp>/Sgsh<em3(IMPC)Tcp>	C57BL/6NCrl-Sgsh<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:5884028	F	MP:0001510	abnormal coat appearance	Slc8b1<em1(IMPC)J>/Slc8b1<em1(IMPC)J>	C57BL/6NJ-Slc8b1<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884028	M	MP:0001417	decreased exploration in new environment	Slc8b1<em1(IMPC)J>/Slc8b1<em1(IMPC)J>	C57BL/6NJ-Slc8b1<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884030	F	MP:0009141	increased prepulse inhibition	Stk36<em1(IMPC)J>/Stk36<+>	C57BL/6NJ-Stk36<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884030	F	MP:0002959	increased urine microalbumin level	Stk36<em1(IMPC)J>/Stk36<+>	C57BL/6NJ-Stk36<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884030	F	MP:0004122	abnormal sinus arrhythmia	Stk36<em1(IMPC)J>/Stk36<+>	C57BL/6NJ-Stk36<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884033	F	MP:0001402	decreased locomotor activity	Wee2<em1(IMPC)J>/Wee2<em1(IMPC)J>	C57BL/6NJ-Wee2<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884033	F	MP:0000063	decreased bone mineral density	Wee2<em1(IMPC)J>/Wee2<em1(IMPC)J>	C57BL/6NJ-Wee2<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884033	F	MP:0004151	decreased circulating iron level	Wee2<em1(IMPC)J>/Wee2<em1(IMPC)J>	C57BL/6NJ-Wee2<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884035	F	MP:0011396	abnormal sleep behavior	Zfyve26<em1(IMPC)J>/Zfyve26<em1(IMPC)J>	C57BL/6NJ-Zfyve26<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884035	M	MP:0002574	increased vertical activity	Zfyve26<em1(IMPC)J>/Zfyve26<em1(IMPC)J>	C57BL/6NJ-Zfyve26<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884035	M	MP:0005562	decreased mean corpuscular hemoglobin	Zfyve26<em1(IMPC)J>/Zfyve26<em1(IMPC)J>	C57BL/6NJ-Zfyve26<em1(IMPC)J>/J	N	MGI:5576271
MGI:5884035	M	MP:0002804	abnormal motor learning	Zfyve26<em1(IMPC)J>/Zfyve26<em1(IMPC)J>	C57BL/6NJ-Zfyve26<em1(IMPC)J>/J	N	MGI:5576271
MGI:5887306	M	MP:0001554	increased circulating free fatty acids level	Arrb2<tm1.1(KOMP)Vlcg>/Arrb2<+>	B6N(Cg)-Arrb2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5887307	F	MP:0013279	increased fasting circulating glucose level	Arrdc1<tm1.1(KOMP)Vlcg>/Arrdc1<+>	B6N(Cg)-Arrdc1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5887311	M	MP:0000195	decreased circulating calcium level	AU021092<tm1b(KOMP)Wtsi>/AU021092<+>	C57BL/6N-AU021092<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5887311	M	MP:0000274	enlarged heart	AU021092<tm1b(KOMP)Wtsi>/AU021092<+>	C57BL/6N-AU021092<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5887311	M	MP:0000266	abnormal heart morphology	AU021092<tm1b(KOMP)Wtsi>/AU021092<+>	C57BL/6N-AU021092<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5887311	M	MP:0001399	hyperactivity	AU021092<tm1b(KOMP)Wtsi>/AU021092<+>	C57BL/6N-AU021092<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5887324	F	MP:0005385	cardiovascular system phenotype	Bicdl1<tm2b(EUCOMM)Wtsi>/Bicdl1<+>	C57BL/6N-Bicdl1<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5887324	F	MP:0003928	increased heart rate variability	Bicdl1<tm2b(EUCOMM)Wtsi>/Bicdl1<+>	C57BL/6N-Bicdl1<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5887333	M	MP:0009142	decreased prepulse inhibition	Chmp3<tm1b(EUCOMM)Hmgu>/Chmp3<+>	C57BL/6N-Chmp3<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5887335	M	MP:0002060	abnormal skin morphology	Cnr1<tm1.1(KOMP)Vlcg>/Cnr1<+>	C57BL/6N-Cnr1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887342	F	MP:0001102	small superior vagus ganglion	Cst3<tm1b(EUCOMM)Wtsi>/Cst3<+>	C57BL/6N-Cst3<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5887364	F	MP:0003917	increased kidney weight	F10<tm1b(EUCOMM)Hmgu>/F10<+>	C57BL/6N-F10<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:5887370	F	MP:0010052	increased grip strength	Fbxw9<tm1b(EUCOMM)Wtsi>/Fbxw9<+>	C57BL/6N-Fbxw9<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5887373	M	MP:0000702	enlarged lymph nodes	Fgf3<tm4b(EUCOMM)Hmgu>/Fgf3<+>	C57BL/6N-Fgf3<tm4b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:5887380	M	MP:0004931	enlarged epididymis	Gas2l1<tm1.1(KOMP)Vlcg>/Gas2l1<+>	C57BL/6N-Gas2l1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887380	M	MP:0002631	abnormal epididymis morphology	Gas2l1<tm1.1(KOMP)Vlcg>/Gas2l1<+>	C57BL/6N-Gas2l1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887419	M	MP:0001147	small testis	Jazf1<tm1b(EUCOMM)Wtsi>/Jazf1<+>	C57BL/6N-Jazf1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5887419	M	MP:0001146	abnormal testis morphology	Jazf1<tm1b(EUCOMM)Wtsi>/Jazf1<+>	C57BL/6N-Jazf1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:5887429	M	MP:0001258	decreased body length	Krt5<tm1.1(KOMP)Vlcg>/Krt5<+>	C57BL/6N-Krt5<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5887429	F	MP:0002339	abnormal lymph node morphology	Krt5<tm1.1(KOMP)Vlcg>/Krt5<+>	C57BL/6N-Krt5<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:5887433	F	MP:0004924	abnormal behavior	Lgi4<tm1.1(KOMP)Vlcg>/Lgi4<+>	C57BL/6N-Lgi4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887433	F	MP:0020870	decreased thigmotaxis	Lgi4<tm1.1(KOMP)Vlcg>/Lgi4<+>	C57BL/6N-Lgi4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887433	F	MP:0001399	hyperactivity	Lgi4<tm1.1(KOMP)Vlcg>/Lgi4<+>	C57BL/6N-Lgi4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887437	M	MP:0000274	enlarged heart	Lst1<tm1.1(KOMP)Vlcg>/Lst1<+>	C57BL/6N-Lst1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887437	M	MP:0000266	abnormal heart morphology	Lst1<tm1.1(KOMP)Vlcg>/Lst1<+>	C57BL/6N-Lst1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887441	M	MP:0003917	increased kidney weight	Mbd6<tm1.1(KOMP)Vlcg>/Mbd6<+>	C57BL/6N-Mbd6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887441	M	MP:0000274	enlarged heart	Mbd6<tm1.1(KOMP)Vlcg>/Mbd6<+>	C57BL/6N-Mbd6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887441	M	MP:0000266	abnormal heart morphology	Mbd6<tm1.1(KOMP)Vlcg>/Mbd6<+>	C57BL/6N-Mbd6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887441	F	MP:0013279	increased fasting circulating glucose level	Mbd6<tm1.1(KOMP)Vlcg>/Mbd6<+>	C57BL/6N-Mbd6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887441	F	MP:0001258	decreased body length	Mbd6<tm1.1(KOMP)Vlcg>/Mbd6<+>	C57BL/6N-Mbd6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887457	F	MP:0000745	tremors	Nos1ap<tm1b(KOMP)Wtsi>/Nos1ap<+>	C57BL/6N-Nos1ap<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5887460	F	MP:0005011	increased eosinophil cell number	Npsr1<tm1b(KOMP)Wtsi>/Npsr1<tm1b(KOMP)Wtsi>	C57BL/6N-Npsr1<tm1b(KOMP)Wtsi>/Rbrc	N	MGI:5576271
MGI:5887465	M	MP:0002606	increased basophil cell number	Otud6b<tm1b(EUCOMM)Wtsi>/Otud6b<+>	C57BL/6N-Otud6b<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:5887468	F	MP:0002941	increased circulating alanine transaminase level	Padi2<tm1b(KOMP)Wtsi>/Padi2<+>	C57BL/6N-Padi2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:5887478	F	MP:0000689	abnormal spleen morphology	Pja2<tm1b(EUCOMM)Wtsi>/Pja2<+>	C57BL/6N-Pja2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:5887484	M	MP:0000274	enlarged heart	Prg3<tm1.1(KOMP)Vlcg>/Prg3<+>	C57BL/6N-Prg3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887484	M	MP:0000266	abnormal heart morphology	Prg3<tm1.1(KOMP)Vlcg>/Prg3<+>	C57BL/6N-Prg3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887495	M	MP:0004931	enlarged epididymis	Ranbp2<tm1.1(KOMP)Vlcg>/Ranbp2<+>	C57BL/6N-Ranbp2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887495	M	MP:0001147	small testis	Ranbp2<tm1.1(KOMP)Vlcg>/Ranbp2<+>	C57BL/6N-Ranbp2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887495	M	MP:0002631	abnormal epididymis morphology	Ranbp2<tm1.1(KOMP)Vlcg>/Ranbp2<+>	C57BL/6N-Ranbp2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887495	M	MP:0001146	abnormal testis morphology	Ranbp2<tm1.1(KOMP)Vlcg>/Ranbp2<+>	C57BL/6N-Ranbp2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:5887506	F	MP:0004122	abnormal sinus arrhythmia	Rptor<tm2b(EUCOMM)Wtsi>/Rptor<+>	C57BL/6N-Rptor<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:5888374	F	MP:0000367	abnormal coat/ hair morphology	Actrt3<tm1.1(KOMP)Vlcg>/Actrt3<tm1.1(KOMP)Vlcg>	B6N(Cg)-Actrt3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888374	F	MP:0001399	hyperactivity	Actrt3<tm1.1(KOMP)Vlcg>/Actrt3<tm1.1(KOMP)Vlcg>	B6N(Cg)-Actrt3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888374	F	MP:0010097	abnormal retina blood vessel morphology	Actrt3<tm1.1(KOMP)Vlcg>/Actrt3<tm1.1(KOMP)Vlcg>	B6N(Cg)-Actrt3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888376	M	MP:0005627	increased circulating potassium level	Arhgef10<tm1.1(KOMP)Vlcg>/Arhgef10<tm1.1(KOMP)Vlcg>	B6N(Cg)-Arhgef10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888376	M	MP:0005560	decreased circulating glucose level	Arhgef10<tm1.1(KOMP)Vlcg>/Arhgef10<tm1.1(KOMP)Vlcg>	B6N(Cg)-Arhgef10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888376	M	MP:0002941	increased circulating alanine transaminase level	Arhgef10<tm1.1(KOMP)Vlcg>/Arhgef10<tm1.1(KOMP)Vlcg>	B6N(Cg)-Arhgef10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888377	M	MP:0002941	increased circulating alanine transaminase level	Arpc5l<tm1.1(KOMP)Vlcg>/Arpc5l<+>	B6N(Cg)-Arpc5l<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888377	F	MP:0013278	decreased fasting circulating glucose level	Arpc5l<tm1.1(KOMP)Vlcg>/Arpc5l<+>	B6N(Cg)-Arpc5l<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888382	F	MP:0001399	hyperactivity	Eif1b<tm1.1(KOMP)Vlcg>/Eif1b<tm1.1(KOMP)Vlcg>	C57BL/6N-Eif1b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888386	M	MP:0002941	increased circulating alanine transaminase level	Esrra<tm1.1(KOMP)Vlcg>/Esrra<tm1.1(KOMP)Vlcg>	C57BL/6N-Esrra<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888386	F	MP:0011954	shortened PQ interval	Esrra<tm1.1(KOMP)Vlcg>/Esrra<tm1.1(KOMP)Vlcg>	C57BL/6N-Esrra<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888386	M	MP:0002757	decreased vertical activity	Esrra<tm1.1(KOMP)Vlcg>/Esrra<tm1.1(KOMP)Vlcg>	C57BL/6N-Esrra<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888398	M	MP:0006243	impaired pupillary reflex	Mrpl22<tm1b(KOMP)Mbp>/Mrpl22<+>	C57BL/6N-Mrpl22<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5888398	F	MP:0013279	increased fasting circulating glucose level	Mrpl22<tm1b(KOMP)Mbp>/Mrpl22<+>	C57BL/6N-Mrpl22<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:5888407	F	MP:0005292	improved glucose tolerance	Rab11a<tm1b(KOMP)Wtsi>/Rab11a<+>	C57BL/6N-Rab11a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5888409	M	MP:0002833	increased heart weight	Rilpl2<tm1b(KOMP)Wtsi>/Rilpl2<tm1b(KOMP)Wtsi>	C57BL/6N-Rilpl2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5888409	M	MP:0005179	decreased circulating cholesterol level	Rilpl2<tm1b(KOMP)Wtsi>/Rilpl2<tm1b(KOMP)Wtsi>	C57BL/6N-Rilpl2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5888409	F	MP:0013279	increased fasting circulating glucose level	Rilpl2<tm1b(KOMP)Wtsi>/Rilpl2<tm1b(KOMP)Wtsi>	C57BL/6N-Rilpl2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5888413	F	MP:0005565	increased blood urea nitrogen level	Snx3<tm1.1(KOMP)Vlcg>/Snx3<+>	C57BL/6N-Snx3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888413	F	MP:0002590	increased mean corpuscular volume	Snx3<tm1.1(KOMP)Vlcg>/Snx3<+>	C57BL/6N-Snx3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888414	F	MP:0010052	increased grip strength	Sp5<tm1b(KOMP)Wtsi>/Sp5<tm1b(KOMP)Wtsi>	C57BL/6N-Sp5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5888414	F	MP:0001399	hyperactivity	Sp5<tm1b(KOMP)Wtsi>/Sp5<tm1b(KOMP)Wtsi>	C57BL/6N-Sp5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5888414	F	MP:0000208	decreased hematocrit	Sp5<tm1b(KOMP)Wtsi>/Sp5<tm1b(KOMP)Wtsi>	C57BL/6N-Sp5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5888414	F	MP:0002574	increased vertical activity	Sp5<tm1b(KOMP)Wtsi>/Sp5<tm1b(KOMP)Wtsi>	C57BL/6N-Sp5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5888414	M	MP:0013278	decreased fasting circulating glucose level	Sp5<tm1b(KOMP)Wtsi>/Sp5<tm1b(KOMP)Wtsi>	C57BL/6N-Sp5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:5888420	F	MP:0011436	decreased urine magnesium level	Tpcn1<tm1.1(KOMP)Vlcg>/Tpcn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Tpcn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888420	F	MP:0002959	increased urine microalbumin level	Tpcn1<tm1.1(KOMP)Vlcg>/Tpcn1<tm1.1(KOMP)Vlcg>	C57BL/6N-Tpcn1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:5888729	M	MP:0004852	decreased testis weight	Cbfa2t2<em1Dare>/Cbfa2t2<em1Dare>	C57BL/6-Cbfa2t2<em1Dare>	N	27281218
MGI:5888729	F	MP:0005158	ovary hypoplasia	Cbfa2t2<em1Dare>/Cbfa2t2<em1Dare>	C57BL/6-Cbfa2t2<em1Dare>	N	27281218
MGI:5888729	M	MP:0002675	asthenozoospermia	Cbfa2t2<em1Dare>/Cbfa2t2<em1Dare>	C57BL/6-Cbfa2t2<em1Dare>	N	27281218
MGI:5888729	F	MP:0001926	female infertility	Cbfa2t2<em1Dare>/Cbfa2t2<em1Dare>	C57BL/6-Cbfa2t2<em1Dare>	N	27281218
MGI:5888729	M	MP:0001156	abnormal spermatogenesis	Cbfa2t2<em1Dare>/Cbfa2t2<em1Dare>	C57BL/6-Cbfa2t2<em1Dare>	N	27281218
MGI:5888729	F	MP:0002777	absent ovarian follicles	Cbfa2t2<em1Dare>/Cbfa2t2<em1Dare>	C57BL/6-Cbfa2t2<em1Dare>	N	27281218
MGI:5888729	M	MP:0002687	oligozoospermia	Cbfa2t2<em1Dare>/Cbfa2t2<em1Dare>	C57BL/6-Cbfa2t2<em1Dare>	N	27281218
MGI:5888729	M	MP:0001147	small testis	Cbfa2t2<em1Dare>/Cbfa2t2<em1Dare>	C57BL/6-Cbfa2t2<em1Dare>	N	27281218
MGI:5888729	M	MP:0004901	decreased male germ cell number	Cbfa2t2<em1Dare>/Cbfa2t2<em1Dare>	C57BL/6-Cbfa2t2<em1Dare>	N	27281218
MGI:5888729	M	MP:0001925	male infertility	Cbfa2t2<em1Dare>/Cbfa2t2<em1Dare>	C57BL/6-Cbfa2t2<em1Dare>	N	27281218
MGI:5888907	M	MP:0003631	nervous system phenotype	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	Y	27701470
MGI:5888907	M	MP:0020507	increased dendritic spine density	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0002733	abnormal thermal nociception	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	27701470
MGI:5888907	M	MP:0009435	abnormal miniature inhibitory postsynaptic currents	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0001900	impaired synaptic plasticity	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	27701470
MGI:5888907	M	MP:0001900	impaired synaptic plasticity	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0009939	abnormal hippocampus neuron morphology	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0009938	abnormal hippocampus granule cell morphology	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0009937	abnormal neuron differentiation	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	27701470
MGI:5888907	M	MP:0001364	decreased anxiety-related response	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0020394	decreased neuronal precursor proliferation	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	27701470
MGI:5888907	M	MP:0001458	abnormal object recognition memory	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	27701470
MGI:5888907	M	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0004981	decreased neuronal precursor cell number	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	27701470
MGI:5888907	M	MP:0008921	increased neurotransmitter release	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0020357	abnormal excitatory synapse morphology	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	27701470
MGI:5888907	M	MP:0008026	abnormal brain white matter morphology	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0002906	increased susceptibility to pharmacologically induced seizures	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0002912	abnormal excitatory postsynaptic potential	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	27701470
MGI:5888907	M	MP:0002912	abnormal excitatory postsynaptic potential	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0002920	decreased paired-pulse facilitation	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0012006	abnormal hippocampus physiology	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0012307	impaired spatial learning	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0031391	increased locomotor activity	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0003631	nervous system phenotype	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	Y	26619789
MGI:5888907	M	MP:0005386	behavior/neurological phenotype	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	Y	27701470
MGI:5888907	M	MP:0001475	reduced long-term depression	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	27701470
MGI:5888907	M	MP:0001475	reduced long-term depression	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0002206	abnormal CNS synaptic transmission	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0014382	increased miniature inhibitory postsynaptic current frequency	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0020335	abnormal dentate gyrus neuron dendrite morphology	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5888907	M	MP:0002175	decreased brain weight	Rbfox3<tm1a(EUCOMM)Hmgu>/Rbfox3<tm1a(EUCOMM)Hmgu>	B6Dnk;B6N-Rbfox3<tm1a(EUCOMM)Hmgu>/H	N	26619789
MGI:5896434	F	MP:0005380	embryo phenotype	Anxa10<em1Siag>/Anxa10<em1Siag>	involves: C57BL/6 * DBA	Y	27881083
MGI:5896434	F	MP:0005389	reproductive system phenotype	Anxa10<em1Siag>/Anxa10<em1Siag>	involves: C57BL/6 * DBA	Y	27881083
MGI:5896434	F	MP:0003718	maternal effect	Anxa10<em1Siag>/Anxa10<em1Siag>	involves: C57BL/6 * DBA	N	27881083
MGI:5896436	F	MP:0003718	maternal effect	Anxa10<em1Siag>/Anxa10<+>	involves: C57BL/6 * DBA	N	27881083
MGI:5896532	F	MP:0001265	decreased body size	Nsdhl<tm1.1Hrm>/Nsdhl<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * CBA	N	25652406
MGI:5896532	F	MP:0001242	hyperkeratosis	Nsdhl<tm1.1Hrm>/Nsdhl<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * CBA	N	25652406
MGI:5896532	F	MP:0002073	abnormal hair growth	Nsdhl<tm1.1Hrm>/Nsdhl<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * CBA	N	25652406
MGI:5896532	F	MP:0005508	abnormal skeleton morphology	Nsdhl<tm1.1Hrm>/Nsdhl<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * CBA	N	25652406
MGI:5896533	M	MP:0001732	postnatal growth retardation	Nsdhl<tm1.1Hrm>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * CBA	N	25652406
MGI:5896534	M	MP:0001393	ataxia	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0009938	abnormal hippocampus granule cell morphology	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0009939	abnormal hippocampus neuron morphology	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0008924	decreased cerebellar granule cell number	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0000812	abnormal dentate gyrus morphology	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0008572	abnormal Purkinje cell dendrite morphology	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0000807	abnormal hippocampus morphology	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0000873	thin external granule cell layer	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0012204	abnormal neuronal stem cell physiology	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0000852	small cerebellum	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0008415	abnormal neurite morphology	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0002083	premature death	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0008283	small hippocampus	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0000788	abnormal cerebral cortex morphology	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0004098	abnormal cerebellar granule cell morphology	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896534	M	MP:0010387	abnormal Bergmann glial cell morphology	Nsdhl<tm1.1Hrm>/Y,Tg(GFAP-cre)25Mes/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	25652406
MGI:5896617	M	MP:0004543	abnormal sperm physiology	Lrrc52<tm1.1(KOMP)Vlcg>/Lrrc52<tm1.1(KOMP)Vlcg>	C57BL/6-Lrrc52<tm1.1(KOMP)Vlcg>	N	25675513
MGI:5896617	M	MP:0000242	impaired fertilization	Lrrc52<tm1.1(KOMP)Vlcg>/Lrrc52<tm1.1(KOMP)Vlcg>	C57BL/6-Lrrc52<tm1.1(KOMP)Vlcg>	N	25675513
MGI:5896617	M	MP:0001922	reduced male fertility	Lrrc52<tm1.1(KOMP)Vlcg>/Lrrc52<tm1.1(KOMP)Vlcg>	C57BL/6-Lrrc52<tm1.1(KOMP)Vlcg>	N	25675513
MGI:5896618	M	MP:0004543	abnormal sperm physiology	Catsper1<tm1Clph>/Catsper1<tm1Clph>,Lrrc52<tm1.1(KOMP)Vlcg>/Lrrc52<tm1.1(KOMP)Vlcg>	involves: 129S4/SvJae * C57BL/6NTac	N	25675513
MGI:5896619	M	MP:0004543	abnormal sperm physiology	Kcnu1<tm1.2Clin>/Kcnu1<tm1.2Clin>	involves: C57BL/6NTac	N	25675513
MGI:5896619	M	MP:0000242	impaired fertilization	Kcnu1<tm1.2Clin>/Kcnu1<tm1.2Clin>	involves: C57BL/6NTac	N	25675513
MGI:5896620	M	MP:0005389	reproductive system phenotype	Kcnu1<tm1.1Clin>/Kcnu1<+>	involves: C57BL/6NTac	Y	25675513
MGI:5896620	M	MP:0004543	abnormal sperm physiology	Kcnu1<tm1.1Clin>/Kcnu1<+>	involves: C57BL/6NTac	N	25675513
MGI:5896995	F	MP:0005389	reproductive system phenotype	Spdya<tm1Kald>/Spdya<tm1Kald>,Tg(Zp3-cre)93Knw/0	involves: 129S1/Sv * C57BL/6J	Y	28031483
MGI:5896996	F	MP:0004833	ovary atrophy	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5896996	M	MP:0010948	abnormal double-strand DNA break repair	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5896996	M	MP:0008261	arrest of male meiosis	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5896996	M	MP:0004901	decreased male germ cell number	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5896996	F	MP:0005431	decreased oocyte number	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5896996	F	MP:0005168	abnormal female meiosis	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5896996	M	MP:0001925	male infertility	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5896996	M	MP:0005169	abnormal male meiosis	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5896996	M	MP:0009451	abnormal chromosomal synapsis	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5896996	F	MP:0001926	female infertility	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5896996	M	MP:0008966	abnormal chiasmata formation	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5896996	M	MP:0003205	testicular atrophy	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5896996	M	MP:0006379	abnormal spermatocyte morphology	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5896996	M	MP:0006380	abnormal spermatid morphology	Spdya<tm1.1Klad>/Spdya<tm1.1Klad>	involves: 129S1/Sv * C57BL/6J	N	28031483
MGI:5897192	M	MP:0014178	increased brain apoptosis	Malat1<tm1.2Dlsp>/Malat1<tm1.2Dlsp>	B6J.Cg-Malat1<tm1.2Dlsp>	N	28093478
MGI:5897192	M	MP:0006060	increased cerebral infarct size	Malat1<tm1.2Dlsp>/Malat1<tm1.2Dlsp>	B6J.Cg-Malat1<tm1.2Dlsp>	N	28093478
MGI:5897192	M	MP:0003633	abnormal nervous system physiology	Malat1<tm1.2Dlsp>/Malat1<tm1.2Dlsp>	B6J.Cg-Malat1<tm1.2Dlsp>	N	28093478
MGI:5897192	M	MP:0003076	increased susceptibility to ischemic brain injury	Malat1<tm1.2Dlsp>/Malat1<tm1.2Dlsp>	B6J.Cg-Malat1<tm1.2Dlsp>	N	28093478
MGI:5897192	M	MP:0001847	brain inflammation	Malat1<tm1.2Dlsp>/Malat1<tm1.2Dlsp>	B6J.Cg-Malat1<tm1.2Dlsp>	N	28093478
MGI:5897237	M	MP:0003691	abnormal microglial cell physiology	Trem2<tm1(KOMP)Vlcg>/Trem2<tm1(KOMP)Vlcg>	C57BL/6N-Trem2<tm1(KOMP)Vlcg>	N	28077724
MGI:5897237	M	MP:0020449	decreased microglial cell activation	Trem2<tm1(KOMP)Vlcg>/Trem2<tm1(KOMP)Vlcg>	C57BL/6N-Trem2<tm1(KOMP)Vlcg>	N	28077724
MGI:5897237	M	MP:0010170	abnormal glial cell apoptosis	Trem2<tm1(KOMP)Vlcg>/Trem2<tm1(KOMP)Vlcg>	C57BL/6N-Trem2<tm1(KOMP)Vlcg>	N	28077724
MGI:5897237	M	MP:0004045	abnormal cell cycle checkpoint function	Trem2<tm1(KOMP)Vlcg>/Trem2<tm1(KOMP)Vlcg>	C57BL/6N-Trem2<tm1(KOMP)Vlcg>	N	28077724
MGI:5897270	F	MP:0004829	increased anti-chromatin antibody level	Lbr<ic-J>/Lbr<+>	(NZW/LacJ x C57BL/6J-Lbr<ic-J>/J)F1	N	27483354
MGI:5897270	F	MP:0005325	abnormal renal glomerulus morphology	Lbr<ic-J>/Lbr<+>	(NZW/LacJ x C57BL/6J-Lbr<ic-J>/J)F1	N	27483354
MGI:5897270	F	MP:0003725	increased autoantibody level	Lbr<ic-J>/Lbr<+>	(NZW/LacJ x C57BL/6J-Lbr<ic-J>/J)F1	N	27483354
MGI:5897270	F	MP:0003215	renal interstitial fibrosis	Lbr<ic-J>/Lbr<+>	(NZW/LacJ x C57BL/6J-Lbr<ic-J>/J)F1	N	27483354
MGI:5897270	F	MP:0002135	abnormal kidney morphology	Lbr<ic-J>/Lbr<+>	(NZW/LacJ x C57BL/6J-Lbr<ic-J>/J)F1	N	27483354
MGI:5897270	F	MP:0004794	increased anti-nuclear antigen antibody level	Lbr<ic-J>/Lbr<+>	(NZW/LacJ x C57BL/6J-Lbr<ic-J>/J)F1	N	27483354
MGI:5897270	F	MP:0004801	increased susceptibility to systemic lupus erythematosus	Lbr<ic-J>/Lbr<+>	(NZW/LacJ x C57BL/6J-Lbr<ic-J>/J)F1	N	27483354
MGI:5897270	F	MP:0000691	enlarged spleen	Lbr<ic-J>/Lbr<+>	(NZW/LacJ x C57BL/6J-Lbr<ic-J>/J)F1	N	27483354
MGI:5897270	F	MP:0005264	glomerulosclerosis	Lbr<ic-J>/Lbr<+>	(NZW/LacJ x C57BL/6J-Lbr<ic-J>/J)F1	N	27483354
MGI:5897348	M	MP:0011101	prenatal lethality, incomplete penetrance	Pgam5<tm1d(EUCOMM)Wtsi>/Pgam5<tm1d(EUCOMM)Wtsi>	involves: C57BL/6N	N	26582950
MGI:5897391	F	MP:0004921	decreased placenta weight	Ada<tm1Mw>/Ada<tm1Mw>,Tg(Afp-ADA)#Xiay/0	involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	N	25538227
MGI:5897391	F	MP:0003231	abnormal placenta vasculature	Ada<tm1Mw>/Ada<tm1Mw>,Tg(Afp-ADA)#Xiay/0	involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	N	25538227
MGI:5897391	F	MP:0002962	increased urine protein level	Ada<tm1Mw>/Ada<tm1Mw>,Tg(Afp-ADA)#Xiay/0	involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	N	25538227
MGI:5897391	F	MP:0004259	small placenta	Ada<tm1Mw>/Ada<tm1Mw>,Tg(Afp-ADA)#Xiay/0	involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	N	25538227
MGI:5897391	F	MP:0006144	increased systemic arterial systolic blood pressure	Ada<tm1Mw>/Ada<tm1Mw>,Tg(Afp-ADA)#Xiay/0	involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	N	25538227
MGI:5897391	F	MP:0000231	hypertension	Ada<tm1Mw>/Ada<tm1Mw>,Tg(Afp-ADA)#Xiay/0	involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	N	25538227
MGI:5897391	F	MP:0001711	abnormal placenta morphology	Ada<tm1Mw>/Ada<tm1Mw>,Tg(Afp-ADA)#Xiay/0	involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	N	25538227
MGI:5897391	F	MP:0005325	abnormal renal glomerulus morphology	Ada<tm1Mw>/Ada<tm1Mw>,Tg(Afp-ADA)#Xiay/0	involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	N	25538227
MGI:5897419	F	MP:0001711	abnormal placenta morphology	Ada<tm1Mw>/Ada<tm1Mw>,Adora2b<tm1Dgen>/Adora2b<tm1Dgen>,Tg(Afp-ADA)#Xiay/0	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	N	25538227
MGI:5897419	F	MP:0005385	cardiovascular system phenotype	Ada<tm1Mw>/Ada<tm1Mw>,Adora2b<tm1Dgen>/Adora2b<tm1Dgen>,Tg(Afp-ADA)#Xiay/0	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	Y	25538227
MGI:5897419	F	MP:0005367	renal/urinary system phenotype	Ada<tm1Mw>/Ada<tm1Mw>,Adora2b<tm1Dgen>/Adora2b<tm1Dgen>,Tg(Afp-ADA)#Xiay/0	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	Y	25538227
MGI:5897605	M	MP:0005311	abnormal circulating amino acid level	Ddah1<tm1.1Geno>/Ddah1<tm1.1Geno>	Not Specified	N	25910799
MGI:5897605	M	MP:0005332	abnormal amino acid level	Ddah1<tm1.1Geno>/Ddah1<tm1.1Geno>	Not Specified	N	25910799
MGI:5897606	M	MP:0003710	abnormal physiological neovascularization	Ddah1<tm1Geno>/Ddah1<tm1Geno>,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	25910799
MGI:5897606	M	MP:0005376	homeostasis/metabolism phenotype	Ddah1<tm1Geno>/Ddah1<tm1Geno>,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	Y	25910799
MGI:5897606	M	MP:0005385	cardiovascular system phenotype	Ddah1<tm1Geno>/Ddah1<tm1Geno>,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	Y	25910799
MGI:5897606	M	MP:0005602	decreased angiogenesis	Ddah1<tm1Geno>/Ddah1<tm1Geno>,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	25910799
MGI:5897617	M	MP:0010033	paraphimosis	Tg(TG-RET/CCDC6)42Cled/0	involves: FVB/N	N	8536638
MGI:5897665	M	MP:0001262	decreased body weight	Arhgap25<tm1a(KOMP)Wtsi>/Arhgap25<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	27566826
MGI:5897675	M	MP:0001263	weight loss	Prkar1a<tm1.2Lsk>/Prkar1a<tm1.2Lsk>,Pten<tm1.1Mwst>/Pten<tm1.1Mwst>,Tg(TPO-cre)1Shk/0	involves: 129S1/Sv * 129X1/SvJ * FVB/NCr	N	24512487
MGI:5897684	M	MP:0020362	abnormal male germ cell physiology	Exd1<tm1Embrp>/Exd1<tm1Embrp>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JRj	N	26669262
MGI:5897825	F	MP:0001926	female infertility	Meioc<tm1a(KOMP)Wtsi>/Meioc<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N * NMRI	N	26742488
MGI:5897825	M	MP:0005159	azoospermia	Meioc<tm1a(KOMP)Wtsi>/Meioc<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N * NMRI	N	26742488
MGI:5897825	M	MP:0001147	small testis	Meioc<tm1a(KOMP)Wtsi>/Meioc<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N * NMRI	N	26742488
MGI:5897825	F	MP:0004805	absent oocytes	Meioc<tm1a(KOMP)Wtsi>/Meioc<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N * NMRI	N	26742488
MGI:5897825	F	MP:0001127	small ovary	Meioc<tm1a(KOMP)Wtsi>/Meioc<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N * NMRI	N	26742488
MGI:5897825	M	MP:0001925	male infertility	Meioc<tm1a(KOMP)Wtsi>/Meioc<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N * NMRI	N	26742488
MGI:5897825	F	MP:0002777	absent ovarian follicles	Meioc<tm1a(KOMP)Wtsi>/Meioc<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N * NMRI	N	26742488
MGI:5897825	M	MP:0008261	arrest of male meiosis	Meioc<tm1a(KOMP)Wtsi>/Meioc<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N * NMRI	N	26742488
MGI:5897825	M	MP:0014052	increased male germ cell apoptosis	Meioc<tm1a(KOMP)Wtsi>/Meioc<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N * NMRI	N	26742488
MGI:5897825	F	MP:0010767	abnormal female meiosis I arrest	Meioc<tm1a(KOMP)Wtsi>/Meioc<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N * NMRI	N	26742488
MGI:5897825	F	MP:0005431	decreased oocyte number	Meioc<tm1a(KOMP)Wtsi>/Meioc<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N * NMRI	N	26742488
MGI:5897825	M	MP:0004901	decreased male germ cell number	Meioc<tm1a(KOMP)Wtsi>/Meioc<tm1a(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N * NMRI	N	26742488
MGI:5897828	M	MP:0001147	small testis	Meioc<tm1c(KOMP)Wtsi>/Meioc<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	26742488
MGI:5897828	F	MP:0001127	small ovary	Meioc<tm1c(KOMP)Wtsi>/Meioc<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	26742488
MGI:5897828	M	MP:0001925	male infertility	Meioc<tm1c(KOMP)Wtsi>/Meioc<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	26742488
MGI:5897828	M	MP:0005159	azoospermia	Meioc<tm1c(KOMP)Wtsi>/Meioc<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	26742488
MGI:5897828	F	MP:0001926	female infertility	Meioc<tm1c(KOMP)Wtsi>/Meioc<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	26742488
MGI:5897828	F	MP:0002777	absent ovarian follicles	Meioc<tm1c(KOMP)Wtsi>/Meioc<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	26742488
MGI:5898142	M	MP:0008261	arrest of male meiosis	4930447C04Rik<em1Amp>/4930447C04Rik<em1Amp>	involves: C57BL/6J * CBA/J	N	27796301
MGI:5898142	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	4930447C04Rik<em1Amp>/4930447C04Rik<em1Amp>	involves: C57BL/6J * CBA/J	N	27796301
MGI:5898142	M	MP:0001147	small testis	4930447C04Rik<em1Amp>/4930447C04Rik<em1Amp>	involves: C57BL/6J * CBA/J	N	27796301
MGI:5898142	M	MP:0005169	abnormal male meiosis	4930447C04Rik<em1Amp>/4930447C04Rik<em1Amp>	involves: C57BL/6J * CBA/J	N	27796301
MGI:5898142	F	MP:0004805	absent oocytes	4930447C04Rik<em1Amp>/4930447C04Rik<em1Amp>	involves: C57BL/6J * CBA/J	N	27796301
MGI:5898142	M	MP:0014052	increased male germ cell apoptosis	4930447C04Rik<em1Amp>/4930447C04Rik<em1Amp>	involves: C57BL/6J * CBA/J	N	27796301
MGI:5898142	M	MP:0002216	abnormal seminiferous tubule morphology	4930447C04Rik<em1Amp>/4930447C04Rik<em1Amp>	involves: C57BL/6J * CBA/J	N	27796301
MGI:5898142	M	MP:0005159	azoospermia	4930447C04Rik<em1Amp>/4930447C04Rik<em1Amp>	involves: C57BL/6J * CBA/J	N	27796301
MGI:5898142	F	MP:0008871	abnormal ovarian follicle number	4930447C04Rik<em1Amp>/4930447C04Rik<em1Amp>	involves: C57BL/6J * CBA/J	N	27796301
MGI:5898142	F	MP:0001926	female infertility	4930447C04Rik<em1Amp>/4930447C04Rik<em1Amp>	involves: C57BL/6J * CBA/J	N	27796301
MGI:5898142	F	MP:0001931	abnormal oogenesis	4930447C04Rik<em1Amp>/4930447C04Rik<em1Amp>	involves: C57BL/6J * CBA/J	N	27796301
MGI:5898142	M	MP:0001925	male infertility	4930447C04Rik<em1Amp>/4930447C04Rik<em1Amp>	involves: C57BL/6J * CBA/J	N	27796301
MGI:5898142	F	MP:0001126	abnormal ovary morphology	4930447C04Rik<em1Amp>/4930447C04Rik<em1Amp>	involves: C57BL/6J * CBA/J	N	27796301
MGI:5898247	F	MP:0001262	decreased body weight	Mogat1<tm1Far>/Mogat1<tm1Far>	involves: 129S4/SvJae	N	26880786
MGI:5898249	F	MP:0011939	increased food intake	Agpat2<tm1Garg>/Agpat2<tm1Garg>,Mogat1<tm1Far>/Mogat1<tm1Far>	involves: 129S4/SvJae * 129S6/SvEvTac	N	26880786
MGI:5898249	M	MP:0005292	improved glucose tolerance	Agpat2<tm1Garg>/Agpat2<tm1Garg>,Mogat1<tm1Far>/Mogat1<tm1Far>	involves: 129S4/SvJae * 129S6/SvEvTac	N	26880786
MGI:5898249	F	MP:0005559	increased circulating glucose level	Agpat2<tm1Garg>/Agpat2<tm1Garg>,Mogat1<tm1Far>/Mogat1<tm1Far>	involves: 129S4/SvJae * 129S6/SvEvTac	N	26880786
MGI:5898250	F	MP:0001552	increased circulating triglyceride level	Lep<ob>/Lep<ob>,Mogat1<tm1Far>/Mogat1<tm1Far>	involves: 129S4/SvJae	N	26880786
MGI:5898250	F	MP:0005559	increased circulating glucose level	Lep<ob>/Lep<ob>,Mogat1<tm1Far>/Mogat1<tm1Far>	involves: 129S4/SvJae	N	26880786
MGI:5898286	M	MP:0005292	improved glucose tolerance	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0010025	decreased total body fat amount	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0002644	decreased circulating triglyceride level	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0000609	abnormal liver physiology	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0005289	increased oxygen consumption	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	F	MP:0002106	abnormal muscle physiology	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0010378	increased respiratory quotient	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0031391	increased locomotor activity	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	F	MP:0002108	abnormal muscle morphology	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0005534	decreased body temperature	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0003981	decreased circulating phospholipid level	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0002702	decreased circulating free fatty acids level	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0005668	decreased circulating leptin level	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0001262	decreased body weight	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	F	MP:0005620	abnormal muscle contractility	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0005179	decreased circulating cholesterol level	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0004889	increased energy expenditure	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0009356	decreased liver triglyceride level	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0002665	decreased circulating corticosterone level	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0001433	polyphagia	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0000652	enlarged sebaceous gland	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0003068	enlarged kidney	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0001258	decreased body length	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898286	M	MP:0008965	increased basal metabolism	Mpzl3<tm1Tacz>/Mpzl3<tm1Tacz>	B6.129P2-Mpzl3<tm1Tacz>	N	23715724
MGI:5898300	M	MP:0001925	male infertility	Mcmdc2<tm3b(EUCOMM)Hmgu>/Mcmdc2<tm3b(EUCOMM)Hmgu>	involves: BALB/c * C57BL/6 * C57BL/6N * CD-1	N	27760146
MGI:5898300	M	MP:0001156	abnormal spermatogenesis	Mcmdc2<tm3b(EUCOMM)Hmgu>/Mcmdc2<tm3b(EUCOMM)Hmgu>	involves: BALB/c * C57BL/6 * C57BL/6N * CD-1	N	27760146
MGI:5898300	F	MP:0004833	ovary atrophy	Mcmdc2<tm3b(EUCOMM)Hmgu>/Mcmdc2<tm3b(EUCOMM)Hmgu>	involves: BALB/c * C57BL/6 * C57BL/6N * CD-1	N	27760146
MGI:5898300	F	MP:0001926	female infertility	Mcmdc2<tm3b(EUCOMM)Hmgu>/Mcmdc2<tm3b(EUCOMM)Hmgu>	involves: BALB/c * C57BL/6 * C57BL/6N * CD-1	N	27760146
MGI:5898300	F	MP:0004805	absent oocytes	Mcmdc2<tm3b(EUCOMM)Hmgu>/Mcmdc2<tm3b(EUCOMM)Hmgu>	involves: BALB/c * C57BL/6 * C57BL/6N * CD-1	N	27760146
MGI:5898300	M	MP:0005159	azoospermia	Mcmdc2<tm3b(EUCOMM)Hmgu>/Mcmdc2<tm3b(EUCOMM)Hmgu>	involves: BALB/c * C57BL/6 * C57BL/6N * CD-1	N	27760146
MGI:5898300	M	MP:0008261	arrest of male meiosis	Mcmdc2<tm3b(EUCOMM)Hmgu>/Mcmdc2<tm3b(EUCOMM)Hmgu>	involves: BALB/c * C57BL/6 * C57BL/6N * CD-1	N	27760146
MGI:5898431	F	MP:0011101	prenatal lethality, incomplete penetrance	Zfp36l3<tm1Pjb>/Zfp36l3<tm1Pjb>	involves: C57BL/6 * C57BL/6NTac	N	26952984
MGI:5898431	F	MP:0001770	abnormal iron level	Zfp36l3<tm1Pjb>/Zfp36l3<tm1Pjb>	involves: C57BL/6 * C57BL/6NTac	N	26952984
MGI:5898431	F	MP:0005380	embryo phenotype	Zfp36l3<tm1Pjb>/Zfp36l3<tm1Pjb>	involves: C57BL/6 * C57BL/6NTac	Y	26952984
MGI:5898431	F	MP:0008770	decreased survivor rate	Zfp36l3<tm1Pjb>/Zfp36l3<tm1Pjb>	involves: C57BL/6 * C57BL/6NTac	N	26952984
MGI:5898431	F	MP:0009615	abnormal zinc homeostasis	Zfp36l3<tm1Pjb>/Zfp36l3<tm1Pjb>	involves: C57BL/6 * C57BL/6NTac	N	26952984
MGI:5898432	F	MP:0003123	paternal imprinting	Zfp36l3<tm1Pjb>/Zfp36l3<+>	involves: C57BL/6 * C57BL/6NTac	N	26952984
MGI:5898432	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Zfp36l3<tm1Pjb>/Zfp36l3<+>	involves: C57BL/6 * C57BL/6NTac	N	26952984
MGI:5898432	F	MP:0008770	decreased survivor rate	Zfp36l3<tm1Pjb>/Zfp36l3<+>	involves: C57BL/6 * C57BL/6NTac	N	26952984
MGI:5898433	M	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance	Zfp36l3<tm1Pjb>/Y	involves: C57BL/6 * C57BL/6NTac	N	26952984
MGI:5898433	M	MP:0001770	abnormal iron level	Zfp36l3<tm1Pjb>/Y	involves: C57BL/6 * C57BL/6NTac	N	26952984
MGI:5898433	M	MP:0008770	decreased survivor rate	Zfp36l3<tm1Pjb>/Y	involves: C57BL/6 * C57BL/6NTac	N	26952984
MGI:5898433	M	MP:0009615	abnormal zinc homeostasis	Zfp36l3<tm1Pjb>/Y	involves: C57BL/6 * C57BL/6NTac	N	26952984
MGI:5898573	M	MP:0000470	abnormal stomach morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<+>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5898574	M	MP:0000689	abnormal spleen morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5898574	M	MP:0002764	short tibia	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5898574	M	MP:0002544	brachydactyly	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5898574	M	MP:0000455	abnormal maxilla morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5898574	M	MP:0002932	abnormal joint morphology	Dnase1l2<tm1.1(KOMP)Wtsi>/Dnase1l2<tm1.1(KOMP)Wtsi>	C57BL/6N-Dnase1l2<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:5901730	F	MP:0004256	abnormal maternal decidual layer morphology	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25043182
MGI:5901730	F	MP:0001711	abnormal placenta morphology	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25043182
MGI:5901730	F	MP:0009352	impaired spacing of implantation sites	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25043182
MGI:5901730	F	MP:0009353	twin decidual capsule	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25043182
MGI:5901730	F	MP:0010039	abnormal trophoblast giant cell proliferation	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25043182
MGI:5901730	F	MP:0009666	abnormal embryo attachment	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25043182
MGI:5901730	F	MP:0009663	abnormal uterine-embryonic axis	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25043182
MGI:5901730	F	MP:0005389	reproductive system phenotype	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	25043182
MGI:5901730	F	MP:0001935	decreased litter size	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25043182
MGI:5901730	F	MP:0001729	impaired embryo implantation	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25043182
MGI:5901730	F	MP:0001923	reduced female fertility	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25043182
MGI:5901730	F	MP:0001120	abnormal uterus morphology	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25043182
MGI:5901730	F	MP:0011521	decreased placental labyrinth size	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25043182
MGI:5901730	F	MP:0001672	abnormal embryo development	Gt(ROSA)26Sor<tm1(CAG-Wnt5a,-AcGFP)Skde>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25043182
MGI:5901756	F	MP:0005517	impaired liver regeneration	Alb<tm1(cre/ERT2)Mtz>/Alb<+>,Hcfc1<tm1Lwh>/Hcfc1<+>	involves: 129S2/SvPas * C57BL/6	N	26921005
MGI:5901759	M	MP:0011092	embryonic lethality, complete penetrance	Hcfc1<tm1Lwh>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901759	M	MP:0001698	decreased embryo size	Hcfc1<tm1Lwh>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901759	M	MP:0013292	embryonic lethality prior to organogenesis	Hcfc1<tm1Lwh>/Y,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901761	F	MP:0002086	abnormal extraembryonic tissue morphology	Hcfc1<tm1Lwh>/Hcfc1<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901761	F	MP:0001258	decreased body length	Hcfc1<tm1Lwh>/Hcfc1<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901761	F	MP:0000352	decreased cell proliferation	Hcfc1<tm1Lwh>/Hcfc1<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901761	F	MP:0006042	increased apoptosis	Hcfc1<tm1Lwh>/Hcfc1<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901761	F	MP:0013292	embryonic lethality prior to organogenesis	Hcfc1<tm1Lwh>/Hcfc1<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901761	F	MP:0014134	abnormal embryo morphology	Hcfc1<tm1Lwh>/Hcfc1<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901761	F	MP:0003961	decreased lean body mass	Hcfc1<tm1Lwh>/Hcfc1<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901761	F	MP:0011092	embryonic lethality, complete penetrance	Hcfc1<tm1Lwh>/Hcfc1<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901761	F	MP:0001698	decreased embryo size	Hcfc1<tm1Lwh>/Hcfc1<+>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901762	F	MP:0002086	abnormal extraembryonic tissue morphology	Hcfc1<tm1Lwh>/Hcfc1<tm1Lwh>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901762	F	MP:0000352	decreased cell proliferation	Hcfc1<tm1Lwh>/Hcfc1<tm1Lwh>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901762	F	MP:0013292	embryonic lethality prior to organogenesis	Hcfc1<tm1Lwh>/Hcfc1<tm1Lwh>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901762	F	MP:0014134	abnormal embryo morphology	Hcfc1<tm1Lwh>/Hcfc1<tm1Lwh>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901762	F	MP:0006042	increased apoptosis	Hcfc1<tm1Lwh>/Hcfc1<tm1Lwh>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901762	F	MP:0001698	decreased embryo size	Hcfc1<tm1Lwh>/Hcfc1<tm1Lwh>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901762	F	MP:0011092	embryonic lethality, complete penetrance	Hcfc1<tm1Lwh>/Hcfc1<tm1Lwh>,Edil3<Tg(Sox2-cre)1Amc>/Edil3<+>	involves: C57BL/6 * CBA	N	26921005
MGI:5901907	F	MP:0001935	decreased litter size	Pgr<tm2(cre)Lyd>/Pgr<+>,Ror1<tm1.1Meg>/Ror1<tm1.1Meg>,Ror2<tm1.1Meg>/Ror2<tm1.1Meg>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	25043182
MGI:5901907	F	MP:0009666	abnormal embryo attachment	Pgr<tm2(cre)Lyd>/Pgr<+>,Ror1<tm1.1Meg>/Ror1<tm1.1Meg>,Ror2<tm1.1Meg>/Ror2<tm1.1Meg>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	25043182
MGI:5901907	F	MP:0001923	reduced female fertility	Pgr<tm2(cre)Lyd>/Pgr<+>,Ror1<tm1.1Meg>/Ror1<tm1.1Meg>,Ror2<tm1.1Meg>/Ror2<tm1.1Meg>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	25043182
MGI:5901907	F	MP:0004256	abnormal maternal decidual layer morphology	Pgr<tm2(cre)Lyd>/Pgr<+>,Ror1<tm1.1Meg>/Ror1<tm1.1Meg>,Ror2<tm1.1Meg>/Ror2<tm1.1Meg>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	25043182
MGI:5901913	F	MP:0009666	abnormal embryo attachment	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	N	25043182
MGI:5901913	F	MP:0011521	decreased placental labyrinth size	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	N	25043182
MGI:5901913	F	MP:0001923	reduced female fertility	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	N	25043182
MGI:5901913	F	MP:0009663	abnormal uterine-embryonic axis	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	N	25043182
MGI:5901913	F	MP:0001935	decreased litter size	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	N	25043182
MGI:5901913	F	MP:0010039	abnormal trophoblast giant cell proliferation	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	N	25043182
MGI:5901913	F	MP:0009353	twin decidual capsule	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	N	25043182
MGI:5901913	F	MP:0009352	impaired spacing of implantation sites	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	N	25043182
MGI:5901913	F	MP:0001729	impaired embryo implantation	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	N	25043182
MGI:5901913	F	MP:0005389	reproductive system phenotype	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	Y	25043182
MGI:5901913	F	MP:0004256	abnormal maternal decidual layer morphology	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	N	25043182
MGI:5901913	F	MP:0001120	abnormal uterus morphology	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	N	25043182
MGI:5901913	F	MP:0001711	abnormal placenta morphology	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	N	25043182
MGI:5901913	F	MP:0001672	abnormal embryo development	Pgr<tm2(cre)Lyd>/Pgr<+>,Wnt5a<tm1.1Tpy>/Wnt5a<tm1.1Tpy>	involves: 129S1/Sv * 129X1/SvJ	N	25043182
MGI:5902066	M	MP:0002687	oligozoospermia	Del(XMagea1-Magea6)1Nju/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	27226137
MGI:5902066	M	MP:0004852	decreased testis weight	Del(XMagea1-Magea6)1Nju/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	27226137
MGI:5902066	M	MP:0014052	increased male germ cell apoptosis	Del(XMagea1-Magea6)1Nju/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	27226137
MGI:5902066	M	MP:0001153	small seminiferous tubules	Del(XMagea1-Magea6)1Nju/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	27226137
MGI:5902066	M	MP:0014040	increased cellular sensitivity to DNA damaging agents	Del(XMagea1-Magea6)1Nju/Y,Tg(EIIa-cre)C5379Lmgd/0	involves: 129S6/SvEvTac * C57BL/6J * FVB/N	N	27226137
MGI:5902071	M	MP:0000818	abnormal amygdala morphology	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902071	M	MP:0008540	abnormal cerebral hemisphere morphology	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	29349289
MGI:5902071	M	MP:0006254	thin cerebral cortex	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	29349289
MGI:5902071	M	MP:0012468	decreased striatum size	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	29349289
MGI:5902071	M	MP:0008414	abnormal spatial reference memory	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902071	M	MP:0002574	increased vertical activity	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902071	M	MP:0031391	increased locomotor activity	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902071	M	MP:0031391	increased locomotor activity	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902071	M	MP:0000774	decreased brain size	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	29349289
MGI:5902071	M	MP:0001393	ataxia	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902071	M	MP:0001405	impaired coordination	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902071	M	MP:0001405	impaired coordination	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902071	M	MP:0002882	abnormal neuron morphology	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902071	M	MP:0008918	microgliosis	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	29349289
MGI:5902071	M	MP:0005386	behavior/neurological phenotype	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	Y	21964919
MGI:5902071	M	MP:0003354	astrocytosis	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	29349289
MGI:5902071	M	MP:0000852	small cerebellum	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	29349289
MGI:5902071	M	MP:0002152	abnormal brain morphology	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902071	M	MP:0000889	abnormal cerebellar molecular layer	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902071	M	MP:0000876	Purkinje cell degeneration	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902071	M	MP:0000876	Purkinje cell degeneration	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902071	M	MP:0000876	Purkinje cell degeneration	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	29349289
MGI:5902071	M	MP:0000849	abnormal cerebellum morphology	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	29349289
MGI:5902071	M	MP:0000807	abnormal hippocampus morphology	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	29349289
MGI:5902071	M	MP:0002183	gliosis	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902071	M	MP:0000818	abnormal amygdala morphology	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902071	M	MP:0005584	abnormal enzyme/coenzyme activity	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902071	M	MP:0031561	increased ganglioside level	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902071	M	MP:0031561	increased ganglioside level	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902071	M	MP:0014329	abnormal Purkinje cell axon morphology	Slc9a6<tm1Dgen>/Y	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902072	F	MP:0014329	abnormal Purkinje cell axon morphology	Slc9a6<tm1Dgen>/Slc9a6<tm1Dgen>	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902072	F	MP:0000876	Purkinje cell degeneration	Slc9a6<tm1Dgen>/Slc9a6<tm1Dgen>	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902072	F	MP:0000818	abnormal amygdala morphology	Slc9a6<tm1Dgen>/Slc9a6<tm1Dgen>	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902072	F	MP:0005386	behavior/neurological phenotype	Slc9a6<tm1Dgen>/Slc9a6<tm1Dgen>	B6.129P2-Slc9a6<tm1Dgen>/J	Y	21964919
MGI:5902072	F	MP:0002152	abnormal brain morphology	Slc9a6<tm1Dgen>/Slc9a6<tm1Dgen>	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902072	F	MP:0012779	abnormal brain cholesterol level	Slc9a6<tm1Dgen>/Slc9a6<tm1Dgen>	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902072	F	MP:0000788	abnormal cerebral cortex morphology	Slc9a6<tm1Dgen>/Slc9a6<tm1Dgen>	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902072	F	MP:0002882	abnormal neuron morphology	Slc9a6<tm1Dgen>/Slc9a6<tm1Dgen>	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902072	F	MP:0011086	postnatal lethality, incomplete penetrance	Slc9a6<tm1Dgen>/Slc9a6<tm1Dgen>	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902072	F	MP:0031561	increased ganglioside level	Slc9a6<tm1Dgen>/Slc9a6<tm1Dgen>	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902072	F	MP:0005584	abnormal enzyme/coenzyme activity	Slc9a6<tm1Dgen>/Slc9a6<tm1Dgen>	B6.129P2-Slc9a6<tm1Dgen>/J	N	21964919
MGI:5902076	F	MP:0002183	gliosis	Slc9a6<tm1Dgen>/Slc9a6<+>	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902076	F	MP:0008414	abnormal spatial reference memory	Slc9a6<tm1Dgen>/Slc9a6<+>	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902076	F	MP:0000818	abnormal amygdala morphology	Slc9a6<tm1Dgen>/Slc9a6<+>	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902076	F	MP:0000876	Purkinje cell degeneration	Slc9a6<tm1Dgen>/Slc9a6<+>	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902076	F	MP:0031561	increased ganglioside level	Slc9a6<tm1Dgen>/Slc9a6<+>	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902076	F	MP:0008267	abnormal hippocampus CA3 region morphology	Slc9a6<tm1Dgen>/Slc9a6<+>	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902076	F	MP:0008269	abnormal hippocampus CA4 region morphology	Slc9a6<tm1Dgen>/Slc9a6<+>	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902076	F	MP:0001405	impaired coordination	Slc9a6<tm1Dgen>/Slc9a6<+>	B6.129P2-Slc9a6<tm1Dgen>/J	N	26515654
MGI:5902076	F	MP:0000880	decreased Purkinje cell number	Slc9a6<tm1Dgen>/Slc9a6<+>	B6.129P2-Slc9a6<tm1Dgen>/J	N	29349289
MGI:5902077	M	MP:0002161	abnormal fertility/fecundity	Rhox13<tm1.2Chge>/Y	involves: 129P2/OlaHsd * C57BL/6N	N	27486269
MGI:5902077	M	MP:0004901	decreased male germ cell number	Rhox13<tm1.2Chge>/Y	involves: 129P2/OlaHsd * C57BL/6N	N	27486269
MGI:5902077	M	MP:0014052	increased male germ cell apoptosis	Rhox13<tm1.2Chge>/Y	involves: 129P2/OlaHsd * C57BL/6N	N	27486269
MGI:5902077	M	MP:0002687	oligozoospermia	Rhox13<tm1.2Chge>/Y	involves: 129P2/OlaHsd * C57BL/6N	N	27486269
MGI:5902077	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Rhox13<tm1.2Chge>/Y	involves: 129P2/OlaHsd * C57BL/6N	N	27486269
MGI:5902139	M	MP:0014143	decreased body fat mass	mt-Nd6<m1Jbst>,mt-Ta<m1Jbst>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	N	27626666
MGI:5902139	M	MP:0006086	decreased body mass index	mt-Nd6<m1Jbst>,mt-Ta<m1Jbst>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	N	27626666
MGI:5902139	M	MP:0003961	decreased lean body mass	mt-Nd6<m1Jbst>,mt-Ta<m1Jbst>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	N	27626666
MGI:5902151	M	MP:0014052	increased male germ cell apoptosis	Rhox13<tm1.2Chge>/Y	B6NCrl.129P2(Cg)-Rhox13<tm1.2Chge>	N	27486269
MGI:5902151	M	MP:0002687	oligozoospermia	Rhox13<tm1.2Chge>/Y	B6NCrl.129P2(Cg)-Rhox13<tm1.2Chge>	N	27486269
MGI:5902151	M	MP:0004901	decreased male germ cell number	Rhox13<tm1.2Chge>/Y	B6NCrl.129P2(Cg)-Rhox13<tm1.2Chge>	N	27486269
MGI:5902324	M	MP:0001925	male infertility	Catsperz<tm1(KOMP)Mbp>/Catsperz<tm1(KOMP)Mbp>	C57BL/6N-Catsperz<tm1(KOMP)Mbp>	N	28226241
MGI:5902324	M	MP:0001919	abnormal reproductive system physiology	Catsperz<tm1(KOMP)Mbp>/Catsperz<tm1(KOMP)Mbp>	C57BL/6N-Catsperz<tm1(KOMP)Mbp>	N	28226241
MGI:5902324	M	MP:0009282	decreased hyperactivated sperm motility	Catsperz<tm1(KOMP)Mbp>/Catsperz<tm1(KOMP)Mbp>	C57BL/6N-Catsperz<tm1(KOMP)Mbp>	N	28226241
MGI:5902324	M	MP:0031011	abnormal sperm migration in female genital tract	Catsperz<tm1(KOMP)Mbp>/Catsperz<tm1(KOMP)Mbp>	C57BL/6N-Catsperz<tm1(KOMP)Mbp>	N	28226241
MGI:5902324	M	MP:0001935	decreased litter size	Catsperz<tm1(KOMP)Mbp>/Catsperz<tm1(KOMP)Mbp>	C57BL/6N-Catsperz<tm1(KOMP)Mbp>	N	28226241
MGI:5902324	M	MP:0001922	reduced male fertility	Catsperz<tm1(KOMP)Mbp>/Catsperz<tm1(KOMP)Mbp>	C57BL/6N-Catsperz<tm1(KOMP)Mbp>	N	28226241
MGI:5902374	M	MP:0012674	tomacula	Cnp<tm1(cre)Kan>/Cnp<+>,Septin8<tm1c(EUCOMM)Wtsi>/Septin8<tm1c(EUCOMM)Wtsi>	B6N.Cg-Septin8<tm1c(EUCOMM)Wtsi> Cnp<tm1(cre)Kan>	N	27504968
MGI:5902374	M	MP:0008814	decreased nerve conduction velocity	Cnp<tm1(cre)Kan>/Cnp<+>,Septin8<tm1c(EUCOMM)Wtsi>/Septin8<tm1c(EUCOMM)Wtsi>	B6N.Cg-Septin8<tm1c(EUCOMM)Wtsi> Cnp<tm1(cre)Kan>	N	27504968
MGI:5902374	M	MP:0003631	nervous system phenotype	Cnp<tm1(cre)Kan>/Cnp<+>,Septin8<tm1c(EUCOMM)Wtsi>/Septin8<tm1c(EUCOMM)Wtsi>	B6N.Cg-Septin8<tm1c(EUCOMM)Wtsi> Cnp<tm1(cre)Kan>	Y	27504968
MGI:5902377	M	MP:0000921	demyelination	Septin8<tm1c(EUCOMM)Wtsi>/Septin8<tm1c(EUCOMM)Wtsi>,Tg(Plp1-cre/ERT2)1Ueli/0	B6N.Cg-Septin8<tm1c(EUCOMM)Wtsi> Tg(Plp1-cre/ERT2)1Ueli	N	27504968
MGI:5902377	M	MP:0012674	tomacula	Septin8<tm1c(EUCOMM)Wtsi>/Septin8<tm1c(EUCOMM)Wtsi>,Tg(Plp1-cre/ERT2)1Ueli/0	B6N.Cg-Septin8<tm1c(EUCOMM)Wtsi> Tg(Plp1-cre/ERT2)1Ueli	N	27504968
MGI:5902379	M	MP:0008814	decreased nerve conduction velocity	Septin8<tm1d(EUCOMM)Wtsi>/Septin8<tm1d(EUCOMM)Wtsi>	B6N(Cg)-Septin8<tm1d(EUCOMM)Wtsi>	N	27504968
MGI:5902379	M	MP:0003631	nervous system phenotype	Septin8<tm1d(EUCOMM)Wtsi>/Septin8<tm1d(EUCOMM)Wtsi>	B6N(Cg)-Septin8<tm1d(EUCOMM)Wtsi>	Y	27504968
MGI:5902379	M	MP:0012674	tomacula	Septin8<tm1d(EUCOMM)Wtsi>/Septin8<tm1d(EUCOMM)Wtsi>	B6N(Cg)-Septin8<tm1d(EUCOMM)Wtsi>	N	27504968
MGI:5902381	M	MP:0012674	tomacula	Plp1<tm1Kan>/Y	B6N.129-Plp1<tm1Kan>	N	27504968
MGI:5902381	M	MP:0013438	dysmyelination	Plp1<tm1Kan>/Y	B6N.129-Plp1<tm1Kan>	N	27504968
MGI:5902381	M	MP:0010047	axonal spheroids	Plp1<tm1Kan>/Y	B6N.129-Plp1<tm1Kan>	N	27504968
MGI:5902383	M	MP:0012674	tomacula	Mag<tm1Mtg>/Mag<tm1Mtg>	B6N.129S2-Mag<tm1Mtg>	N	27504968
MGI:5902383	M	MP:0013438	dysmyelination	Mag<tm1Mtg>/Mag<tm1Mtg>	B6N.129S2-Mag<tm1Mtg>	N	27504968
MGI:5902385	M	MP:0013438	dysmyelination	Cnp<tm1(cre)Kan>/Cnp<tm1(cre)Kan>	B6N.129-Cnp<tm1(cre)Kan>	N	27504968
MGI:5902385	M	MP:0012674	tomacula	Cnp<tm1(cre)Kan>/Cnp<tm1(cre)Kan>	B6N.129-Cnp<tm1(cre)Kan>	N	27504968
MGI:5902385	M	MP:0005405	axon degeneration	Cnp<tm1(cre)Kan>/Cnp<tm1(cre)Kan>	B6N.129-Cnp<tm1(cre)Kan>	N	27504968
MGI:5902387	M	MP:0012674	tomacula	Cnp<tm1(cre)Kan>/Cnp<+>,Pten<tm1Hwu>/Pten<tm1Hwu>	B6N.129-Cnp<tm1(cre)Kan> Pten<tm1Hwu>	N	27504968
MGI:5902395	M	MP:0002702	decreased circulating free fatty acids level	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902395	M	MP:0005659	decreased susceptibility to diet-induced obesity	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902395	M	MP:0009356	decreased liver triglyceride level	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902395	M	MP:0010026	decreased liver cholesterol level	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902395	M	MP:0009283	decreased gonadal fat pad weight	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902395	M	MP:0002628	hepatic steatosis	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902395	M	MP:0002644	decreased circulating triglyceride level	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902395	M	MP:0001399	hyperactivity	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902395	M	MP:0002079	increased circulating insulin level	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902395	M	MP:0009355	increased liver triglyceride level	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902395	M	MP:0005331	insulin resistance	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902395	M	MP:0014143	decreased body fat mass	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902395	M	MP:0005293	impaired glucose tolerance	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902395	M	MP:0008844	decreased subcutaneous adipose tissue amount	C1qtnf1<tm1Lex>/C1qtnf1<tm1Lex>	B6.129S5-C1qtnf1<tm1Lex>	N	27555298
MGI:5902401	F	MP:0009459	skeletal muscle hyperplasia	Mstn<tm3.1Sjl>/Mstn<tm3.1Sjl>,Tg(CDX2-cre)101Erf/0	B6.Cg-Mstn<tm3.1Sjl> Tg(CDX2-cre)101Erf/Sjl	N	26769954
MGI:5902401	F	MP:0009461	skeletal muscle hypertrophy	Mstn<tm3.1Sjl>/Mstn<tm3.1Sjl>,Tg(CDX2-cre)101Erf/0	B6.Cg-Mstn<tm3.1Sjl> Tg(CDX2-cre)101Erf/Sjl	N	26769954
MGI:5902987	F	MP:0013618	decreased areal bone mineral density	Lrp5<tvrm111B>/Lrp5<tvrm111B>	C57BL/6J-Lrp5<tvrm111b>/Pjn	N	28356706
MGI:5902987	F	MP:0010124	decreased bone mineral content	Lrp5<tvrm111B>/Lrp5<tvrm111B>	C57BL/6J-Lrp5<tvrm111b>/Pjn	N	28356706
MGI:5903433	M	MP:0005565	increased blood urea nitrogen level	Cldn2<tm1Lex>/Y	B6J.129S5-Cldn2<tm1Lex>	N	27214555
MGI:5903433	M	MP:0005319	abnormal enzyme/coenzyme level	Cldn2<tm1Lex>/Y	B6J.129S5-Cldn2<tm1Lex>	N	27214555
MGI:5903433	M	MP:0005039	hypoxia	Cldn2<tm1Lex>/Y	B6J.129S5-Cldn2<tm1Lex>	N	27214555
MGI:5903433	M	MP:0006316	increased urine sodium level	Cldn2<tm1Lex>/Y	B6J.129S5-Cldn2<tm1Lex>	N	27214555
MGI:5903433	M	MP:0005289	increased oxygen consumption	Cldn2<tm1Lex>/Y	B6J.129S5-Cldn2<tm1Lex>	N	27214555
MGI:5903433	M	MP:0011442	abnormal renal sodium ion transport	Cldn2<tm1Lex>/Y	B6J.129S5-Cldn2<tm1Lex>	N	27214555
MGI:5903433	M	MP:0010109	abnormal renal sodium reabsorption	Cldn2<tm1Lex>/Y	B6J.129S5-Cldn2<tm1Lex>	N	27214555
MGI:5903433	M	MP:0005553	increased circulating creatinine level	Cldn2<tm1Lex>/Y	B6J.129S5-Cldn2<tm1Lex>	N	27214555
MGI:5903433	M	MP:0004041	increased susceptibility to kidney reperfusion injury	Cldn2<tm1Lex>/Y	B6J.129S5-Cldn2<tm1Lex>	N	27214555
MGI:5903485	M	MP:0001922	reduced male fertility	Sirt1<tm3.1Mcby>/Sirt1<tm3.1Mcby>	involves: 129/Sv * 129S1/Sv * 129S4/SvJae * 129X1/SvJ	N	28273169
MGI:5903626	M	MP:0002007	increased cellular sensitivity to gamma-irradiation	Poln<tm1.2Rwd>/Poln<tm1.2Rwd>,Polq<tm1Jcs>/Polq<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	N	28570559
MGI:5903634	M	MP:0009754	enhanced behavioral response to cocaine	Oprk1<tm1.1Waca>/Oprk1<tm1.1Waca>,Tg(Slc6a3-icre)9075Gsc/0	B6J.Cg-Oprk1<tm1.1Waca> Tg(Slc6a3-icre)9075Gsc	N	23446450
MGI:5903634	M	MP:0005386	behavior/neurological phenotype	Oprk1<tm1.1Waca>/Oprk1<tm1.1Waca>,Tg(Slc6a3-icre)9075Gsc/0	B6J.Cg-Oprk1<tm1.1Waca> Tg(Slc6a3-icre)9075Gsc	Y	23446450
MGI:5903634	M	MP:0001364	decreased anxiety-related response	Oprk1<tm1.1Waca>/Oprk1<tm1.1Waca>,Tg(Slc6a3-icre)9075Gsc/0	B6J.Cg-Oprk1<tm1.1Waca> Tg(Slc6a3-icre)9075Gsc	N	23446450
MGI:5903636	M	MP:0005386	behavior/neurological phenotype	Oprk1<tm1.2Waca>/Oprk1<tm1.2Waca>	B6J.B6NTac(Cg)-Oprk1<tm1.2Waca>	Y	23446450
MGI:5903636	M	MP:0001982	decreased chemically-elicited antinociception	Oprk1<tm1.2Waca>/Oprk1<tm1.2Waca>	B6J.B6NTac(Cg)-Oprk1<tm1.2Waca>	N	23446450
MGI:5903776	F	MP:0005560	decreased circulating glucose level	Kl<ecalc1>/Kl<ecalc1>	involves: C3H/HeH * C57BL/6J	N	25860694
MGI:5903776	M	MP:0005419	decreased circulating serum albumin level	Kl<ecalc1>/Kl<ecalc1>	involves: C3H/HeH * C57BL/6J	N	25860694
MGI:5903905	M	MP:0003651	abnormal axon extension	Musk<tm1.2Ics>/Musk<tm1.2Ics>	involves: BALB/cN * C57BL/6NTac	N	25810523
MGI:5903905	M	MP:0000748	progressive muscle weakness	Musk<tm1.2Ics>/Musk<tm1.2Ics>	involves: BALB/cN * C57BL/6NTac	N	25810523
MGI:5903905	M	MP:0012055	abnormal phrenic nerve innervation pattern to diaphragm	Musk<tm1.2Ics>/Musk<tm1.2Ics>	involves: BALB/cN * C57BL/6NTac	N	25810523
MGI:5903905	M	MP:0000160	kyphosis	Musk<tm1.2Ics>/Musk<tm1.2Ics>	involves: BALB/cN * C57BL/6NTac	N	25810523
MGI:5903905	M	MP:0008415	abnormal neurite morphology	Musk<tm1.2Ics>/Musk<tm1.2Ics>	involves: BALB/cN * C57BL/6NTac	N	25810523
MGI:5903905	M	MP:0003646	increased muscle fatigability	Musk<tm1.2Ics>/Musk<tm1.2Ics>	involves: BALB/cN * C57BL/6NTac	N	25810523
MGI:5903905	M	MP:0010053	decreased grip strength	Musk<tm1.2Ics>/Musk<tm1.2Ics>	involves: BALB/cN * C57BL/6NTac	N	25810523
MGI:5903905	M	MP:0004174	abnormal spine curvature	Musk<tm1.2Ics>/Musk<tm1.2Ics>	involves: BALB/cN * C57BL/6NTac	N	25810523
MGI:5903905	M	MP:0001053	abnormal neuromuscular synapse morphology	Musk<tm1.2Ics>/Musk<tm1.2Ics>	involves: BALB/cN * C57BL/6NTac	N	25810523
MGI:5903929	M	MP:0014172	decreased fatty acid oxidation	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5903929	M	MP:0010378	increased respiratory quotient	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5903929	M	MP:0005292	improved glucose tolerance	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5903929	M	MP:0031414	decreased skeletal muscle triglyceride level	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5903929	M	MP:0031417	decreased cardiac muscle triglyceride level	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5903929	M	MP:0010399	decreased skeletal muscle glycogen level	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5903929	M	MP:0013243	abnormal carbohydrate metabolism	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5903929	M	MP:0014171	increased fatty acid oxidation	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5903929	M	MP:0008034	enhanced lipolysis	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5903929	M	MP:0002891	increased insulin sensitivity	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5903929	M	MP:0009823	abnormal sphingomyelin level	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5903929	M	MP:0030017	decreased adipocyte glucose uptake	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5903929	M	MP:0005331	insulin resistance	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5903929	M	MP:0012232	abnormal ceramide level	Plin5<tm1e(KOMP)Wtsi>/Plin5<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	25161888
MGI:5904009	M	MP:0020351	decreased vocalization	Lrfn2<tm1.1Jaru>/Lrfn2<tm1.1Jaru>	B6J.129P2-Lrfn2<tm1.1Jaru>	N	28604739
MGI:5904161	M	MP:0004852	decreased testis weight	Tg(Stra8-icre)1Reb/0,Zscan21<tm1.1Jiwa>/Zscan21<tm1.1Jiwa>	involves: FVB/NJ	N	27492080
MGI:5904161	M	MP:0001925	male infertility	Tg(Stra8-icre)1Reb/0,Zscan21<tm1.1Jiwa>/Zscan21<tm1.1Jiwa>	involves: FVB/NJ	N	27492080
MGI:5904161	M	MP:0008261	arrest of male meiosis	Tg(Stra8-icre)1Reb/0,Zscan21<tm1.1Jiwa>/Zscan21<tm1.1Jiwa>	involves: FVB/NJ	N	27492080
MGI:5904161	M	MP:0010948	abnormal double-strand DNA break repair	Tg(Stra8-icre)1Reb/0,Zscan21<tm1.1Jiwa>/Zscan21<tm1.1Jiwa>	involves: FVB/NJ	N	27492080
MGI:5904161	M	MP:0006380	abnormal spermatid morphology	Tg(Stra8-icre)1Reb/0,Zscan21<tm1.1Jiwa>/Zscan21<tm1.1Jiwa>	involves: FVB/NJ	N	27492080
MGI:5904161	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Tg(Stra8-icre)1Reb/0,Zscan21<tm1.1Jiwa>/Zscan21<tm1.1Jiwa>	involves: FVB/NJ	N	27492080
MGI:5904161	M	MP:0006379	abnormal spermatocyte morphology	Tg(Stra8-icre)1Reb/0,Zscan21<tm1.1Jiwa>/Zscan21<tm1.1Jiwa>	involves: FVB/NJ	N	27492080
MGI:5904165	M	MP:0006379	abnormal spermatocyte morphology	Gorasp2<tm1.1Maal>/Gorasp2<tm1.1Maal>	B6J.129S2(Cg)-Gorasp2<tm1.1Maal>	N	28617811
MGI:5904165	M	MP:0001932	abnormal spermiogenesis	Gorasp2<tm1.1Maal>/Gorasp2<tm1.1Maal>	B6J.129S2(Cg)-Gorasp2<tm1.1Maal>	N	28617811
MGI:5904165	M	MP:0001925	male infertility	Gorasp2<tm1.1Maal>/Gorasp2<tm1.1Maal>	B6J.129S2(Cg)-Gorasp2<tm1.1Maal>	N	28617811
MGI:5904165	M	MP:0009831	abnormal sperm midpiece morphology	Gorasp2<tm1.1Maal>/Gorasp2<tm1.1Maal>	B6J.129S2(Cg)-Gorasp2<tm1.1Maal>	N	28617811
MGI:5904165	M	MP:0008898	abnormal acrosome morphology	Gorasp2<tm1.1Maal>/Gorasp2<tm1.1Maal>	B6J.129S2(Cg)-Gorasp2<tm1.1Maal>	N	28617811
MGI:5904165	M	MP:0009230	abnormal sperm head morphology	Gorasp2<tm1.1Maal>/Gorasp2<tm1.1Maal>	B6J.129S2(Cg)-Gorasp2<tm1.1Maal>	N	28617811
MGI:5904165	M	MP:0002675	asthenozoospermia	Gorasp2<tm1.1Maal>/Gorasp2<tm1.1Maal>	B6J.129S2(Cg)-Gorasp2<tm1.1Maal>	N	28617811
MGI:5904165	M	MP:0002687	oligozoospermia	Gorasp2<tm1.1Maal>/Gorasp2<tm1.1Maal>	B6J.129S2(Cg)-Gorasp2<tm1.1Maal>	N	28617811
MGI:5904165	M	MP:0011743	abnormal Golgi apparatus morphology	Gorasp2<tm1.1Maal>/Gorasp2<tm1.1Maal>	B6J.129S2(Cg)-Gorasp2<tm1.1Maal>	N	28617811
MGI:5904250	F	MP:0010862	decreased respiratory mucosa goblet cell number	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	B6.Cg-Ndor1<Tg(UBC-cre/ERT2)1Ejb> Igf1r<tm1Jcbr>	N	28207927
MGI:5904250	F	MP:0020254	decreased collagen level	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	B6.Cg-Ndor1<Tg(UBC-cre/ERT2)1Ejb> Igf1r<tm1Jcbr>	N	28207927
MGI:5904250	F	MP:0005597	decreased susceptibility to type I hypersensitivity reaction	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	B6.Cg-Ndor1<Tg(UBC-cre/ERT2)1Ejb> Igf1r<tm1Jcbr>	N	28207927
MGI:5904250	F	MP:0002335	decreased airway responsiveness	Igf1r<tm1Jcbr>/Igf1r<tm1Jcbr>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/0	B6.Cg-Ndor1<Tg(UBC-cre/ERT2)1Ejb> Igf1r<tm1Jcbr>	N	28207927
MGI:5904627	M	MP:0004009	abnormal diastolic filling velocity	Tg(Myh6-MYL2*N47K)#Dsc/0	involves: C57BL/6 * SJL	N	19150977
MGI:5904627	M	MP:0001544	abnormal cardiovascular system physiology	Tg(Myh6-MYL2*N47K)#Dsc/0	involves: C57BL/6 * SJL	N	19150977
MGI:5904627	M	MP:0003393	decreased cardiac output	Tg(Myh6-MYL2*N47K)#Dsc/0	involves: C57BL/6 * SJL	N	19150977
MGI:5904628	M	MP:0004009	abnormal diastolic filling velocity	Tg(Myh6-MYL2*R58Q)#Dsc/0	involves: C57BL/6 * SJL	N	19150977
MGI:5904628	M	MP:0020419	decreased cardiac muscle relaxation	Tg(Myh6-MYL2*R58Q)#Dsc/0	involves: C57BL/6 * SJL	N	19150977
MGI:5904628	M	MP:0001544	abnormal cardiovascular system physiology	Tg(Myh6-MYL2*R58Q)#Dsc/0	involves: C57BL/6 * SJL	N	19150977
MGI:5904628	M	MP:0004215	abnormal myocardial fiber physiology	Tg(Myh6-MYL2*R58Q)#Dsc/0	involves: C57BL/6 * SJL	N	19150977
MGI:5904628	M	MP:0000343	abnormal response to cardiac infarction	Tg(Myh6-MYL2*R58Q)#Dsc/0	involves: C57BL/6 * SJL	N	19150977
MGI:5904628	M	MP:0003393	decreased cardiac output	Tg(Myh6-MYL2*R58Q)#Dsc/0	involves: C57BL/6 * SJL	N	19150977
MGI:5904628	M	MP:0002972	abnormal cardiac muscle contractility	Tg(Myh6-MYL2*R58Q)#Dsc/0	involves: C57BL/6 * SJL	N	19150977
MGI:5905888	M	MP:0005324	ascites	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5905888	M	MP:0011925	abnormal heart echocardiography feature	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5905888	M	MP:0001853	heart inflammation	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5905888	M	MP:0010334	pleural effusion	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5905888	M	MP:0000278	abnormal myocardial fiber morphology	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5905888	M	MP:0004090	abnormal sarcomere morphology	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5905888	M	MP:0005608	cardiac interstitial fibrosis	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5905888	M	MP:0004091	abnormal Z line morphology	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5905888	M	MP:0008772	increased heart ventricle size	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5905888	M	MP:0004121	abnormal sarcolemma morphology	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5905888	M	MP:0008725	increased heart atrium size	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5905888	M	MP:0006267	abnormal intercalated disk morphology	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5905888	M	MP:0002795	dilated cardiomyopathy	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5905888	M	MP:0031633	decreased heart left ventricle muscle contractility	A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>,Tg(Myh6-2A)#Know/0	involves: BALB/c * C57BL/6 * FVB/N	N	17190866
MGI:5906002	M	MP:0006036	abnormal mitochondrial physiology	Gt(ROSA)26Sor<tm1(CAG-Nr2f2)Tsa>/Gt(ROSA)26Sor<+>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	26356605
MGI:5906002	M	MP:0001544	abnormal cardiovascular system physiology	Gt(ROSA)26Sor<tm1(CAG-Nr2f2)Tsa>/Gt(ROSA)26Sor<+>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	26356605
MGI:5906002	M	MP:0002795	dilated cardiomyopathy	Gt(ROSA)26Sor<tm1(CAG-Nr2f2)Tsa>/Gt(ROSA)26Sor<+>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	26356605
MGI:5906002	M	MP:0005290	decreased oxygen consumption	Gt(ROSA)26Sor<tm1(CAG-Nr2f2)Tsa>/Gt(ROSA)26Sor<+>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	26356605
MGI:5906002	M	MP:0010955	abnormal respiratory electron transport chain	Gt(ROSA)26Sor<tm1(CAG-Nr2f2)Tsa>/Gt(ROSA)26Sor<+>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	26356605
MGI:5906002	M	MP:0010959	abnormal oxidative phosphorylation	Gt(ROSA)26Sor<tm1(CAG-Nr2f2)Tsa>/Gt(ROSA)26Sor<+>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	26356605
MGI:5906002	M	MP:0000274	enlarged heart	Gt(ROSA)26Sor<tm1(CAG-Nr2f2)Tsa>/Gt(ROSA)26Sor<+>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	26356605
MGI:5906002	M	MP:0014172	decreased fatty acid oxidation	Gt(ROSA)26Sor<tm1(CAG-Nr2f2)Tsa>/Gt(ROSA)26Sor<+>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	26356605
MGI:5906002	M	MP:0005140	decreased cardiac muscle contractility	Gt(ROSA)26Sor<tm1(CAG-Nr2f2)Tsa>/Gt(ROSA)26Sor<+>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	26356605
MGI:5906002	M	MP:0011633	abnormal mitochondrial shape	Gt(ROSA)26Sor<tm1(CAG-Nr2f2)Tsa>/Gt(ROSA)26Sor<+>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	26356605
MGI:5906002	M	MP:0011634	abnormal mitochondrial inner membrane morphology	Gt(ROSA)26Sor<tm1(CAG-Nr2f2)Tsa>/Gt(ROSA)26Sor<+>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	26356605
MGI:5906002	M	MP:0005621	abnormal cell physiology	Gt(ROSA)26Sor<tm1(CAG-Nr2f2)Tsa>/Gt(ROSA)26Sor<+>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	26356605
MGI:5906002	M	MP:0002083	premature death	Gt(ROSA)26Sor<tm1(CAG-Nr2f2)Tsa>/Gt(ROSA)26Sor<+>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	26356605
MGI:5906030	M	MP:0010633	myocardium hypertrophy	Tg(Myh6-Tpm1*D175N)#Dfw/0	Not Specified	N	10400910
MGI:5906030	M	MP:0004564	increased myocardial fiber size	Tg(Myh6-Tpm1*D175N)#Dfw/0	Not Specified	N	10400910
MGI:5906030	M	MP:0001855	abnormal atrial thrombosis	Tg(Myh6-Tpm1*D175N)#Dfw/0	Not Specified	N	10400910
MGI:5906030	M	MP:0000281	abnormal interventricular septum morphology	Tg(Myh6-Tpm1*D175N)#Dfw/0	Not Specified	N	10400910
MGI:5906203	M	MP:0030022	decreased muscle cell glucose uptake	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Ckmm-cre)5Khn/0	involves: 129S1/Sv * 129X1/SvJ * FVB	N	19001090
MGI:5906203	M	MP:0020346	abnormal myocardial fiber calcium currents	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Ckmm-cre)5Khn/0	involves: 129S1/Sv * 129X1/SvJ * FVB	N	19001090
MGI:5906203	M	MP:0006138	congestive heart failure	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Ckmm-cre)5Khn/0	involves: 129S1/Sv * 129X1/SvJ * FVB	N	19001090
MGI:5906203	M	MP:0002795	dilated cardiomyopathy	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Ckmm-cre)5Khn/0	involves: 129S1/Sv * 129X1/SvJ * FVB	N	19001090
MGI:5906203	M	MP:0004564	increased myocardial fiber size	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Ckmm-cre)5Khn/0	involves: 129S1/Sv * 129X1/SvJ * FVB	N	19001090
MGI:5906203	M	MP:0011925	abnormal heart echocardiography feature	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Ckmm-cre)5Khn/0	involves: 129S1/Sv * 129X1/SvJ * FVB	N	19001090
MGI:5906203	M	MP:0031633	decreased heart left ventricle muscle contractility	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Ckmm-cre)5Khn/0	involves: 129S1/Sv * 129X1/SvJ * FVB	N	19001090
MGI:5906203	M	MP:0000274	enlarged heart	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Ckmm-cre)5Khn/0	involves: 129S1/Sv * 129X1/SvJ * FVB	N	19001090
MGI:5906203	M	MP:0008772	increased heart ventricle size	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Ckmm-cre)5Khn/0	involves: 129S1/Sv * 129X1/SvJ * FVB	N	19001090
MGI:5906203	M	MP:0030020	decreased cardiac muscle cell glucose uptake	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Ckmm-cre)5Khn/0	involves: 129S1/Sv * 129X1/SvJ * FVB	N	19001090
MGI:5906203	M	MP:0002079	increased circulating insulin level	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Ckmm-cre)5Khn/0	involves: 129S1/Sv * 129X1/SvJ * FVB	N	19001090
MGI:5906250	M	MP:0002891	increased insulin sensitivity	Ppp1r3c<tm1Adpr>/Ppp1r3c<tm1Adpr>	B6.Cg-Ppp1r3c<tm1Adpr>	N	MGI:5906245
MGI:5906283	M	MP:0008713	abnormal cytokine level	Tg(APCS-Ifng)5Imeg/0	involves: C57BL/6 * DBA/2	N	17556594
MGI:5906377	M	MP:0002833	increased heart weight	Ptger4<tm1.1Matb>/Ptger4<tm1.1Matb>,Tg(Myh6-cre)2182Mds/0	involves: 129S6/SvEvTac * FVB/N	N	20008274
MGI:5906377	M	MP:0001853	heart inflammation	Ptger4<tm1.1Matb>/Ptger4<tm1.1Matb>,Tg(Myh6-cre)2182Mds/0	involves: 129S6/SvEvTac * FVB/N	N	20008274
MGI:5906377	M	MP:0010630	abnormal cardiac muscle tissue morphology	Ptger4<tm1.1Matb>/Ptger4<tm1.1Matb>,Tg(Myh6-cre)2182Mds/0	involves: 129S6/SvEvTac * FVB/N	N	20008274
MGI:5906377	M	MP:0005608	cardiac interstitial fibrosis	Ptger4<tm1.1Matb>/Ptger4<tm1.1Matb>,Tg(Myh6-cre)2182Mds/0	involves: 129S6/SvEvTac * FVB/N	N	20008274
MGI:5906377	M	MP:0001625	cardiac hypertrophy	Ptger4<tm1.1Matb>/Ptger4<tm1.1Matb>,Tg(Myh6-cre)2182Mds/0	involves: 129S6/SvEvTac * FVB/N	N	20008274
MGI:5906377	M	MP:0000278	abnormal myocardial fiber morphology	Ptger4<tm1.1Matb>/Ptger4<tm1.1Matb>,Tg(Myh6-cre)2182Mds/0	involves: 129S6/SvEvTac * FVB/N	N	20008274
MGI:5906377	M	MP:0014316	decreased heart left ventricle posterior wall thickness	Ptger4<tm1.1Matb>/Ptger4<tm1.1Matb>,Tg(Myh6-cre)2182Mds/0	involves: 129S6/SvEvTac * FVB/N	N	20008274
MGI:5907185	M	MP:0005293	impaired glucose tolerance	Vps13c<tm1.1Geno>/Vps13c<tm1.1Geno>	involves: C57BL/6	N	27329800
MGI:5907185	F	MP:0003562	abnormal pancreatic beta cell physiology	Vps13c<tm1.1Geno>/Vps13c<tm1.1Geno>	involves: C57BL/6	N	27329800
MGI:5907185	F	MP:0002727	decreased circulating insulin level	Vps13c<tm1.1Geno>/Vps13c<tm1.1Geno>	involves: C57BL/6	N	27329800
MGI:5907206	M	MP:0005140	decreased cardiac muscle contractility	Ilk<tm1Star>/Ilk<tm1Star>,Tg(Ckmm-cre)1Lrsn/0	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	16951252
MGI:5907206	M	MP:0011925	abnormal heart echocardiography feature	Ilk<tm1Star>/Ilk<tm1Star>,Tg(Ckmm-cre)1Lrsn/0	involves: 129S1/Sv * 129X1/SvJ * FVB/N	N	16951252
MGI:5907236	M	MP:0011633	abnormal mitochondrial shape	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0003915	increased heart left ventricle weight	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0002953	thick ventricular wall	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0000278	abnormal myocardial fiber morphology	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0010955	abnormal respiratory electron transport chain	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0006038	increased mitochondrial fission	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0010959	abnormal oxidative phosphorylation	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0011628	increased mitochondrial number	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0011925	abnormal heart echocardiography feature	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0006035	abnormal mitochondrial morphology	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0000266	abnormal heart morphology	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0004564	increased myocardial fiber size	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0006321	increased myocardial fiber number	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0002626	increased heart rate	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907236	M	MP:0001625	cardiac hypertrophy	Tg(Myh6-Htr2b)1Lum/0	involves: CD-1	N	12810613
MGI:5907446	M	MP:0011086	postnatal lethality, incomplete penetrance	Cap2<tm1e(EUCOMM)Wtsi>/Cap2<tm1e(EUCOMM)Wtsi>	C57BL/6N-Cap2<tm1e(EUCOMM)Wtsi>	N	22945801
MGI:5907465	M	MP:0000274	enlarged heart	Lpl<tm1Bres>/Lpl<+>,Tg(Myh6-LPL*)357Ijg/0	involves: 129S4/SvJae	N	12569168
MGI:5907465	F	MP:0002833	increased heart weight	Lpl<tm1Bres>/Lpl<+>,Tg(Myh6-LPL*)357Ijg/0	involves: 129S4/SvJae	N	12569168
MGI:5907611	M	MP:0004485	increased response of heart to induced stress	Tg(MT2A-TGFBR2)#Rser/0	involves: C57BL/6 * DBA	N	19933419
MGI:5907611	M	MP:0000350	abnormal cell proliferation	Tg(MT2A-TGFBR2)#Rser/0	involves: C57BL/6 * DBA	N	19933419
MGI:5907611	M	MP:0000266	abnormal heart morphology	Tg(MT2A-TGFBR2)#Rser/0	involves: C57BL/6 * DBA	N	19933419
MGI:5907611	M	MP:0002753	dilated heart left ventricle	Tg(MT2A-TGFBR2)#Rser/0	involves: C57BL/6 * DBA	N	19933419
MGI:5907611	M	MP:0011925	abnormal heart echocardiography feature	Tg(MT2A-TGFBR2)#Rser/0	involves: C57BL/6 * DBA	N	19933419
MGI:5907611	M	MP:0005140	decreased cardiac muscle contractility	Tg(MT2A-TGFBR2)#Rser/0	involves: C57BL/6 * DBA	N	19933419
MGI:5907611	M	MP:0002795	dilated cardiomyopathy	Tg(MT2A-TGFBR2)#Rser/0	involves: C57BL/6 * DBA	N	19933419
MGI:5907647	M	MP:0012688	abnormal heart ventricles weight	Tg(HBx-HCV)C5Tto/0	involves: C57BL/6 * DBA/2	N	15618537
MGI:5907647	M	MP:0011633	abnormal mitochondrial shape	Tg(HBx-HCV)C5Tto/0	involves: C57BL/6 * DBA/2	N	15618537
MGI:5907647	M	MP:0011925	abnormal heart echocardiography feature	Tg(HBx-HCV)C5Tto/0	involves: C57BL/6 * DBA/2	N	15618537
MGI:5907647	M	MP:0002753	dilated heart left ventricle	Tg(HBx-HCV)C5Tto/0	involves: C57BL/6 * DBA/2	N	15618537
MGI:5907647	M	MP:0000266	abnormal heart morphology	Tg(HBx-HCV)C5Tto/0	involves: C57BL/6 * DBA/2	N	15618537
MGI:5907647	M	MP:0005140	decreased cardiac muscle contractility	Tg(HBx-HCV)C5Tto/0	involves: C57BL/6 * DBA/2	N	15618537
MGI:5907647	M	MP:0005330	cardiomyopathy	Tg(HBx-HCV)C5Tto/0	involves: C57BL/6 * DBA/2	N	15618537
MGI:5907647	M	MP:0000278	abnormal myocardial fiber morphology	Tg(HBx-HCV)C5Tto/0	involves: C57BL/6 * DBA/2	N	15618537
MGI:5907647	M	MP:0003141	cardiac fibrosis	Tg(HBx-HCV)C5Tto/0	involves: C57BL/6 * DBA/2	N	15618537
MGI:5907647	M	MP:0004564	increased myocardial fiber size	Tg(HBx-HCV)C5Tto/0	involves: C57BL/6 * DBA/2	N	15618537
MGI:5907647	M	MP:0010630	abnormal cardiac muscle tissue morphology	Tg(HBx-HCV)C5Tto/0	involves: C57BL/6 * DBA/2	N	15618537
MGI:5907647	M	MP:0004091	abnormal Z line morphology	Tg(HBx-HCV)C5Tto/0	involves: C57BL/6 * DBA/2	N	15618537
MGI:5907679	F	MP:0011130	absent tertiary ovarian follicles	E330023G01Rik<Tn(pb-Act-RFP)1.1Zhu>/E330023G01Rik<Tn(pb-Act-RFP)1.1Zhu>	involves: FVB/N	N	24565867
MGI:5907679	F	MP:0011129	decreased tertiary ovarian follicle number	E330023G01Rik<Tn(pb-Act-RFP)1.1Zhu>/E330023G01Rik<Tn(pb-Act-RFP)1.1Zhu>	involves: FVB/N	N	24565867
MGI:5907679	F	MP:0001121	uterus hypoplasia	E330023G01Rik<Tn(pb-Act-RFP)1.1Zhu>/E330023G01Rik<Tn(pb-Act-RFP)1.1Zhu>	involves: FVB/N	N	24565867
MGI:5907679	F	MP:0001129	impaired ovarian folliculogenesis	E330023G01Rik<Tn(pb-Act-RFP)1.1Zhu>/E330023G01Rik<Tn(pb-Act-RFP)1.1Zhu>	involves: FVB/N	N	24565867
MGI:5907679	F	MP:0001127	small ovary	E330023G01Rik<Tn(pb-Act-RFP)1.1Zhu>/E330023G01Rik<Tn(pb-Act-RFP)1.1Zhu>	involves: FVB/N	N	24565867
MGI:5907679	F	MP:0001923	reduced female fertility	E330023G01Rik<Tn(pb-Act-RFP)1.1Zhu>/E330023G01Rik<Tn(pb-Act-RFP)1.1Zhu>	involves: FVB/N	N	24565867
MGI:5908019	M	MP:0005238	increased brain size	Del(7Chrna7-Fan1)1Mima/+	C57BL/6N-Del(7Chrna7-Fan1)1Mima	N	26658876
MGI:5908019	M	MP:0004994	abnormal brain wave pattern	Del(7Chrna7-Fan1)1Mima/+	C57BL/6N-Del(7Chrna7-Fan1)1Mima	N	26658876
MGI:5908019	M	MP:0002176	increased brain weight	Del(7Chrna7-Fan1)1Mima/+	C57BL/6N-Del(7Chrna7-Fan1)1Mima	N	26658876
MGI:5908019	M	MP:0003631	nervous system phenotype	Del(7Chrna7-Fan1)1Mima/+	C57BL/6N-Del(7Chrna7-Fan1)1Mima	Y	26658876
MGI:5908019	M	MP:0008535	enlarged lateral ventricles	Del(7Chrna7-Fan1)1Mima/+	C57BL/6N-Del(7Chrna7-Fan1)1Mima	N	26658876
MGI:5908275	F	MP:0010620	thick mitral valve	Tg(Myh6*)1Lnwd/0	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908275	F	MP:0011925	abnormal heart echocardiography feature	Tg(Myh6*)1Lnwd/0	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908275	F	MP:0020409	abnormal cardiac thrombosis	Tg(Myh6*)1Lnwd/0	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908275	F	MP:0002953	thick ventricular wall	Tg(Myh6*)1Lnwd/0	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908275	F	MP:0000266	abnormal heart morphology	Tg(Myh6*)1Lnwd/0	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908275	F	MP:0010551	abnormal coronary vessel morphology	Tg(Myh6*)1Lnwd/0	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908275	F	MP:0002190	disorganized myocardium	Tg(Myh6*)1Lnwd/0	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908275	F	MP:0002624	abnormal tricuspid valve morphology	Tg(Myh6*)1Lnwd/0	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908349	F	MP:0002833	increased heart weight	Tg(Myh6*)1Lnwd/Tg(Myh6*)1Lnwd	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908349	F	MP:0020409	abnormal cardiac thrombosis	Tg(Myh6*)1Lnwd/Tg(Myh6*)1Lnwd	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908349	F	MP:0002953	thick ventricular wall	Tg(Myh6*)1Lnwd/Tg(Myh6*)1Lnwd	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908349	F	MP:0010620	thick mitral valve	Tg(Myh6*)1Lnwd/Tg(Myh6*)1Lnwd	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908349	F	MP:0010551	abnormal coronary vessel morphology	Tg(Myh6*)1Lnwd/Tg(Myh6*)1Lnwd	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908349	F	MP:0011925	abnormal heart echocardiography feature	Tg(Myh6*)1Lnwd/Tg(Myh6*)1Lnwd	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908349	F	MP:0000266	abnormal heart morphology	Tg(Myh6*)1Lnwd/Tg(Myh6*)1Lnwd	involves: C57BL/6 * FVB/N	N	10362699
MGI:5908398	M	MP:0001262	decreased body weight	Srebf2<tm1Jdh>/Srebf2<tm1Jdh>,Speer6-ps1<Tg(Alb-cre)21Mgn>/?	involves: 129S6/SvEvTac * C57BL/6 * DBA	N	28244871
MGI:5908398	M	MP:0010026	decreased liver cholesterol level	Srebf2<tm1Jdh>/Srebf2<tm1Jdh>,Speer6-ps1<Tg(Alb-cre)21Mgn>/?	involves: 129S6/SvEvTac * C57BL/6 * DBA	N	28244871
MGI:5908398	M	MP:0009356	decreased liver triglyceride level	Srebf2<tm1Jdh>/Srebf2<tm1Jdh>,Speer6-ps1<Tg(Alb-cre)21Mgn>/?	involves: 129S6/SvEvTac * C57BL/6 * DBA	N	28244871
MGI:5908398	M	MP:0005179	decreased circulating cholesterol level	Srebf2<tm1Jdh>/Srebf2<tm1Jdh>,Speer6-ps1<Tg(Alb-cre)21Mgn>/?	involves: 129S6/SvEvTac * C57BL/6 * DBA	N	28244871
MGI:5908398	M	MP:0002118	abnormal lipid homeostasis	Srebf2<tm1Jdh>/Srebf2<tm1Jdh>,Speer6-ps1<Tg(Alb-cre)21Mgn>/?	involves: 129S6/SvEvTac * C57BL/6 * DBA	N	28244871
MGI:5908398	M	MP:0002644	decreased circulating triglyceride level	Srebf2<tm1Jdh>/Srebf2<tm1Jdh>,Speer6-ps1<Tg(Alb-cre)21Mgn>/?	involves: 129S6/SvEvTac * C57BL/6 * DBA	N	28244871
MGI:5908554	M	MP:0001993	abnormal blinking	Tnfrsf14<tm1Kro>/Tnfrsf14<tm1Kro>	C57BL/6-Tnfrsf14<tm1Kro>	N	28114589
MGI:5908554	M	MP:0020917	decreased susceptibility to Herpesvirales infection	Tnfrsf14<tm1Kro>/Tnfrsf14<tm1Kro>	C57BL/6-Tnfrsf14<tm1Kro>	N	28114589
MGI:5908557	M	MP:0020917	decreased susceptibility to Herpesvirales infection	Commd10<Tg(Vav1-icre)A2Kio>/?,Tnfrsf14<tm1.1Kro>/Tnfrsf14<tm1.1Kro>	involves: C57BL/6NCrl * C57BL/10 * CBA * SJL	N	28114589
MGI:5908557	M	MP:0001993	abnormal blinking	Commd10<Tg(Vav1-icre)A2Kio>/?,Tnfrsf14<tm1.1Kro>/Tnfrsf14<tm1.1Kro>	involves: C57BL/6NCrl * C57BL/10 * CBA * SJL	N	28114589
MGI:5909088	M	MP:0008726	increased heart left atrium size	Tg(Myh7-Ptpn11*Q510E)#Krnz/0	FVB/N-Tg(Myh7-Ptpn11*Q510E)#Krnz	N	22058153
MGI:5909088	M	MP:0011925	abnormal heart echocardiography feature	Tg(Myh7-Ptpn11*Q510E)#Krnz/0	FVB/N-Tg(Myh7-Ptpn11*Q510E)#Krnz	N	22058153
MGI:5909088	M	MP:0031633	decreased heart left ventricle muscle contractility	Tg(Myh7-Ptpn11*Q510E)#Krnz/0	FVB/N-Tg(Myh7-Ptpn11*Q510E)#Krnz	N	22058153
MGI:5909332	F	MP:0004485	increased response of heart to induced stress	Tg(Myh6-Tnni3*R146G)121Rbns/0	Not Specified	N	11055985
MGI:5909332	F	MP:0001625	cardiac hypertrophy	Tg(Myh6-Tnni3*R146G)121Rbns/0	Not Specified	N	11055985
MGI:5909332	F	MP:0000278	abnormal myocardial fiber morphology	Tg(Myh6-Tnni3*R146G)121Rbns/0	Not Specified	N	11055985
MGI:5909332	F	MP:0005608	cardiac interstitial fibrosis	Tg(Myh6-Tnni3*R146G)121Rbns/0	Not Specified	N	11055985
MGI:5909415	F	MP:0001260	increased body weight	Ttc9<tm1Vcl>/Ttc9<tm1Vcl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	25798063
MGI:5909415	F	MP:0004952	increased spleen weight	Ttc9<tm1Vcl>/Ttc9<tm1Vcl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	25798063
MGI:5909415	F	MP:0000708	thymus hyperplasia	Ttc9<tm1Vcl>/Ttc9<tm1Vcl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	25798063
MGI:5909415	F	MP:0004955	increased thymus weight	Ttc9<tm1Vcl>/Ttc9<tm1Vcl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	25798063
MGI:5909415	F	MP:0000662	abnormal branching of the mammary ductal tree	Ttc9<tm1Vcl>/Ttc9<tm1Vcl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	25798063
MGI:5909416	F	MP:0000708	thymus hyperplasia	Ttc9<tm1Vcl>/Ttc9<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	25798063
MGI:5910025	F	MP:0001926	female infertility	Bcas2<tm1.1Lil>/Bcas2<tm1.1Lil>,Tg(Zp3-cre)3Mrt/0	involves: 129 * C57BL/6 * FVB/N * SJL	N	26428007
MGI:5910025	F	MP:0003718	maternal effect	Bcas2<tm1.1Lil>/Bcas2<tm1.1Lil>,Tg(Zp3-cre)3Mrt/0	involves: 129 * C57BL/6 * FVB/N * SJL	N	26428007
MGI:5910363	F	MP:0001129	impaired ovarian folliculogenesis	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	B6.129P2-Vrk1<Gt(RRR178)Byg>	N	22741057
MGI:5910363	F	MP:0031381	decreased secondary ovarian follicle number	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	B6.129P2-Vrk1<Gt(RRR178)Byg>	N	22741057
MGI:5910363	F	MP:0014011	abnormal ovary tissue architecture	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	B6.129P2-Vrk1<Gt(RRR178)Byg>	N	22741057
MGI:5910363	F	MP:0011129	decreased tertiary ovarian follicle number	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	B6.129P2-Vrk1<Gt(RRR178)Byg>	N	22741057
MGI:5910363	M	MP:0008995	early reproductive senescence	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	B6.129P2-Vrk1<Gt(RRR178)Byg>	N	21277975
MGI:5910363	F	MP:0001926	female infertility	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	B6.129P2-Vrk1<Gt(RRR178)Byg>	N	21277975
MGI:5910363	F	MP:0001125	abnormal oocyte morphology	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	B6.129P2-Vrk1<Gt(RRR178)Byg>	N	22741057
MGI:5910363	M	MP:0001925	male infertility	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	B6.129P2-Vrk1<Gt(RRR178)Byg>	N	21277975
MGI:5911422	M	MP:0020419	decreased cardiac muscle relaxation	Hrc<tm1.1Desa>/Hrc<tm1.1Desa>	Not Specified	N	28859293
MGI:5911422	M	MP:0002083	premature death	Hrc<tm1.1Desa>/Hrc<tm1.1Desa>	Not Specified	N	28859293
MGI:5911422	M	MP:0004485	increased response of heart to induced stress	Hrc<tm1.1Desa>/Hrc<tm1.1Desa>	Not Specified	N	28859293
MGI:5911422	M	MP:0001636	irregular heartbeat	Hrc<tm1.1Desa>/Hrc<tm1.1Desa>	Not Specified	N	28859293
MGI:5911422	M	MP:0008950	ventricular tachycardia	Hrc<tm1.1Desa>/Hrc<tm1.1Desa>	Not Specified	N	28859293
MGI:5911422	M	MP:0002753	dilated heart left ventricle	Hrc<tm1.1Desa>/Hrc<tm1.1Desa>	Not Specified	N	28859293
MGI:5911422	M	MP:0005140	decreased cardiac muscle contractility	Hrc<tm1.1Desa>/Hrc<tm1.1Desa>	Not Specified	N	28859293
MGI:5911422	M	MP:0004215	abnormal myocardial fiber physiology	Hrc<tm1.1Desa>/Hrc<tm1.1Desa>	Not Specified	N	28859293
MGI:5911422	M	MP:0020345	abnormal myocardial fiber currents	Hrc<tm1.1Desa>/Hrc<tm1.1Desa>	Not Specified	N	28859293
MGI:5911422	M	MP:0009732	ventricular premature beat	Hrc<tm1.1Desa>/Hrc<tm1.1Desa>	Not Specified	N	28859293
MGI:5911422	M	MP:0010754	abnormal heart left ventricle pressure	Hrc<tm1.1Desa>/Hrc<tm1.1Desa>	Not Specified	N	28859293
MGI:5911422	M	MP:0011925	abnormal heart echocardiography feature	Hrc<tm1.1Desa>/Hrc<tm1.1Desa>	Not Specified	N	28859293
MGI:5911687	F	MP:0005168	abnormal female meiosis	Ythdc2<em1Chhe>/Ythdc2<em1Chhe>	involves: BALB/c * C57BL/6J	N	28809393
MGI:5911687	F	MP:0001926	female infertility	Ythdc2<em1Chhe>/Ythdc2<em1Chhe>	involves: BALB/c * C57BL/6J	N	28809393
MGI:5911687	M	MP:0001925	male infertility	Ythdc2<em1Chhe>/Ythdc2<em1Chhe>	involves: BALB/c * C57BL/6J	N	28809393
MGI:5911687	M	MP:0008261	arrest of male meiosis	Ythdc2<em1Chhe>/Ythdc2<em1Chhe>	involves: BALB/c * C57BL/6J	N	28809393
MGI:5911687	M	MP:0014052	increased male germ cell apoptosis	Ythdc2<em1Chhe>/Ythdc2<em1Chhe>	involves: BALB/c * C57BL/6J	N	28809393
MGI:5911687	M	MP:0001147	small testis	Ythdc2<em1Chhe>/Ythdc2<em1Chhe>	involves: BALB/c * C57BL/6J	N	28809393
MGI:5911687	M	MP:0005159	azoospermia	Ythdc2<em1Chhe>/Ythdc2<em1Chhe>	involves: BALB/c * C57BL/6J	N	28809393
MGI:5911687	F	MP:0001127	small ovary	Ythdc2<em1Chhe>/Ythdc2<em1Chhe>	involves: BALB/c * C57BL/6J	N	28809393
MGI:5911688	F	MP:0001127	small ovary	Ythdc2<em2Chhe>/Ythdc2<em2Chhe>	involves: BALB/c * C57BL/6J	N	28809393
MGI:5911688	M	MP:0005159	azoospermia	Ythdc2<em2Chhe>/Ythdc2<em2Chhe>	involves: BALB/c * C57BL/6J	N	28809393
MGI:5911688	F	MP:0001926	female infertility	Ythdc2<em2Chhe>/Ythdc2<em2Chhe>	involves: BALB/c * C57BL/6J	N	28809393
MGI:5911688	M	MP:0001147	small testis	Ythdc2<em2Chhe>/Ythdc2<em2Chhe>	involves: BALB/c * C57BL/6J	N	28809393
MGI:5911688	M	MP:0001925	male infertility	Ythdc2<em2Chhe>/Ythdc2<em2Chhe>	involves: BALB/c * C57BL/6J	N	28809393
MGI:5911692	M	MP:0001925	male infertility	Ythdc2<em1Embrp>/Ythdc2<em1Embrp>	involves: C57BL/6J	N	29033321
MGI:5911692	M	MP:0014052	increased male germ cell apoptosis	Ythdc2<em1Embrp>/Ythdc2<em1Embrp>	involves: C57BL/6J	N	29033321
MGI:5911692	F	MP:0004833	ovary atrophy	Ythdc2<em1Embrp>/Ythdc2<em1Embrp>	involves: C57BL/6J	N	29033321
MGI:5911692	M	MP:0003205	testicular atrophy	Ythdc2<em1Embrp>/Ythdc2<em1Embrp>	involves: C57BL/6J	N	29033321
MGI:5911692	F	MP:0001926	female infertility	Ythdc2<em1Embrp>/Ythdc2<em1Embrp>	involves: C57BL/6J	N	29033321
MGI:5911692	F	MP:0005431	decreased oocyte number	Ythdc2<em1Embrp>/Ythdc2<em1Embrp>	involves: C57BL/6J	N	29033321
MGI:5911692	F	MP:0005168	abnormal female meiosis	Ythdc2<em1Embrp>/Ythdc2<em1Embrp>	involves: C57BL/6J	N	29033321
MGI:5911692	M	MP:0005159	azoospermia	Ythdc2<em1Embrp>/Ythdc2<em1Embrp>	involves: C57BL/6J	N	29033321
MGI:5911692	F	MP:0002777	absent ovarian follicles	Ythdc2<em1Embrp>/Ythdc2<em1Embrp>	involves: C57BL/6J	N	29033321
MGI:5911692	M	MP:0008261	arrest of male meiosis	Ythdc2<em1Embrp>/Ythdc2<em1Embrp>	involves: C57BL/6J	N	29033321
MGI:5911692	F	MP:0001131	abnormal ovarian follicle morphology	Ythdc2<em1Embrp>/Ythdc2<em1Embrp>	involves: C57BL/6J	N	29033321
MGI:5911695	F	MP:0001153	small seminiferous tubules	Ythdc2<ketu>/Ythdc2<ketu>	involves: C57BL/6J * FVB/NJ	N	29360036
MGI:5911695	F	MP:0001127	small ovary	Ythdc2<ketu>/Ythdc2<ketu>	involves: C57BL/6J * FVB/NJ	N	29360036
MGI:5911695	M	MP:0001925	male infertility	Ythdc2<ketu>/Ythdc2<ketu>	involves: C57BL/6J * FVB/NJ	N	29360036
MGI:5911695	M	MP:0008261	arrest of male meiosis	Ythdc2<ketu>/Ythdc2<ketu>	involves: C57BL/6J * FVB/NJ	N	29360036
MGI:5911695	M	MP:0005159	azoospermia	Ythdc2<ketu>/Ythdc2<ketu>	involves: C57BL/6J * FVB/NJ	N	29360036
MGI:5911695	M	MP:0014052	increased male germ cell apoptosis	Ythdc2<ketu>/Ythdc2<ketu>	involves: C57BL/6J * FVB/NJ	N	29360036
MGI:5911695	F	MP:0001926	female infertility	Ythdc2<ketu>/Ythdc2<ketu>	involves: C57BL/6J * FVB/NJ	N	29360036
MGI:5911695	M	MP:0004852	decreased testis weight	Ythdc2<ketu>/Ythdc2<ketu>	involves: C57BL/6J * FVB/NJ	N	29360036
MGI:5911696	M	MP:0004852	decreased testis weight	Ythdc2<em1Sky>/Ythdc2<em1Sky>	involves: C57BL/6J * CBA	N	29360036
MGI:5911696	M	MP:0008261	arrest of male meiosis	Ythdc2<em1Sky>/Ythdc2<em1Sky>	involves: C57BL/6J * CBA	N	29360036
MGI:5911696	F	MP:0001926	female infertility	Ythdc2<em1Sky>/Ythdc2<em1Sky>	involves: C57BL/6J * CBA	N	29360036
MGI:5911696	M	MP:0001925	male infertility	Ythdc2<em1Sky>/Ythdc2<em1Sky>	involves: C57BL/6J * CBA	N	29360036
MGI:5911696	F	MP:0001127	small ovary	Ythdc2<em1Sky>/Ythdc2<em1Sky>	involves: C57BL/6J * CBA	N	29360036
MGI:5911698	M	MP:0001925	male infertility	Ythdc2<em1Sky>/Ythdc2<ketu>	involves: C57BL/6J * CBA * FVB/NJ	N	29360036
MGI:5911698	M	MP:0004852	decreased testis weight	Ythdc2<em1Sky>/Ythdc2<ketu>	involves: C57BL/6J * CBA * FVB/NJ	N	29360036
MGI:5911743	F	MP:0001926	female infertility	Ythdf2<tm1.1Doca>/Ythdf2<tm1.1Doca>,Tg(Zp3-cre)3Mrt/0	involves: FVB/N	N	28867294
MGI:5911744	F	MP:0001926	female infertility	Ythdf2<tm1.2Doca>/Ythdf2<tm1.2Doca>	involves: FVB/N	N	28867294
MGI:5911744	M	MP:0005389	reproductive system phenotype	Ythdf2<tm1.2Doca>/Ythdf2<tm1.2Doca>	involves: FVB/N	Y	28867294
MGI:5911801	F	MP:0012010	parturition failure	Cdk5rap2<an>/Cdk5rap2<an>,Tyrp1<B-lt>/Tyrp1<B-lt>	WBB6F1	N	1756209
MGI:5911874	M	MP:0002795	dilated cardiomyopathy	Sgcd<tm1Ojml>/Sgcd<+>	B6.129-Sgcd<tm1Ojml>	N	23695275
MGI:5911874	M	MP:0003061	decreased aerobic running capacity	Sgcd<tm1Ojml>/Sgcd<+>	B6.129-Sgcd<tm1Ojml>	N	23695275
MGI:5911874	M	MP:0012735	abnormal response to exercise	Sgcd<tm1Ojml>/Sgcd<+>	B6.129-Sgcd<tm1Ojml>	N	23695275
MGI:5911874	M	MP:0002833	increased heart weight	Sgcd<tm1Ojml>/Sgcd<+>	B6.129-Sgcd<tm1Ojml>	N	23695275
MGI:5911952	F	MP:0005389	reproductive system phenotype	Henmt1<pin>/Henmt1<pin>	involves: C57BL/6J * CBA	Y	26496356
MGI:5911952	M	MP:0004182	abnormal spermiation	Henmt1<pin>/Henmt1<pin>	involves: C57BL/6J * CBA	N	26496356
MGI:5911952	M	MP:0001925	male infertility	Henmt1<pin>/Henmt1<pin>	involves: C57BL/6J * CBA	N	26496356
MGI:5911952	M	MP:0002675	asthenozoospermia	Henmt1<pin>/Henmt1<pin>	involves: C57BL/6J * CBA	N	26496356
MGI:5911952	M	MP:0009232	abnormal sperm nucleus morphology	Henmt1<pin>/Henmt1<pin>	involves: C57BL/6J * CBA	N	26496356
MGI:5911952	M	MP:0002687	oligozoospermia	Henmt1<pin>/Henmt1<pin>	involves: C57BL/6J * CBA	N	26496356
MGI:5911952	M	MP:0009239	short sperm flagellum	Henmt1<pin>/Henmt1<pin>	involves: C57BL/6J * CBA	N	26496356
MGI:5911952	M	MP:0009376	abnormal manchette morphology	Henmt1<pin>/Henmt1<pin>	involves: C57BL/6J * CBA	N	26496356
MGI:5911952	M	MP:0009236	pinhead sperm	Henmt1<pin>/Henmt1<pin>	involves: C57BL/6J * CBA	N	26496356
MGI:5911952	M	MP:0009833	absent sperm mitochondrial sheath	Henmt1<pin>/Henmt1<pin>	involves: C57BL/6J * CBA	N	26496356
MGI:5911952	M	MP:0004852	decreased testis weight	Henmt1<pin>/Henmt1<pin>	involves: C57BL/6J * CBA	N	26496356
MGI:5911997	F	MP:0005431	decreased oocyte number	Ythdc2<em2Embrp>/Ythdc2<em2Embrp>	involves: C57BL/6J	N	29033321
MGI:5911997	M	MP:0001925	male infertility	Ythdc2<em2Embrp>/Ythdc2<em2Embrp>	involves: C57BL/6J	N	29033321
MGI:5911997	F	MP:0001926	female infertility	Ythdc2<em2Embrp>/Ythdc2<em2Embrp>	involves: C57BL/6J	N	29033321
MGI:5911997	F	MP:0002777	absent ovarian follicles	Ythdc2<em2Embrp>/Ythdc2<em2Embrp>	involves: C57BL/6J	N	29033321
MGI:5911997	M	MP:0005159	azoospermia	Ythdc2<em2Embrp>/Ythdc2<em2Embrp>	involves: C57BL/6J	N	29033321
MGI:5911997	M	MP:0014052	increased male germ cell apoptosis	Ythdc2<em2Embrp>/Ythdc2<em2Embrp>	involves: C57BL/6J	N	29033321
MGI:5911997	F	MP:0005168	abnormal female meiosis	Ythdc2<em2Embrp>/Ythdc2<em2Embrp>	involves: C57BL/6J	N	29033321
MGI:5911997	M	MP:0003205	testicular atrophy	Ythdc2<em2Embrp>/Ythdc2<em2Embrp>	involves: C57BL/6J	N	29033321
MGI:5911997	F	MP:0001131	abnormal ovarian follicle morphology	Ythdc2<em2Embrp>/Ythdc2<em2Embrp>	involves: C57BL/6J	N	29033321
MGI:5911997	M	MP:0008261	arrest of male meiosis	Ythdc2<em2Embrp>/Ythdc2<em2Embrp>	involves: C57BL/6J	N	29033321
MGI:5911997	F	MP:0004833	ovary atrophy	Ythdc2<em2Embrp>/Ythdc2<em2Embrp>	involves: C57BL/6J	N	29033321
MGI:5912041	F	MP:0003915	increased heart left ventricle weight	Des<tm1Cba>/Des<tm1Cba>	involves: 129S2/SvPas * C57BL/6J	N	11827695
MGI:5912041	F	MP:0002837	dystrophic cardiac calcinosis	Des<tm1Cba>/Des<tm1Cba>	involves: 129S2/SvPas * C57BL/6J	N	11827695
MGI:5912041	F	MP:0004215	abnormal myocardial fiber physiology	Des<tm1Cba>/Des<tm1Cba>	involves: 129S2/SvPas * C57BL/6J	N	11827695
MGI:5912041	F	MP:0003141	cardiac fibrosis	Des<tm1Cba>/Des<tm1Cba>	involves: 129S2/SvPas * C57BL/6J	N	11827695
MGI:5912041	F	MP:0002833	increased heart weight	Des<tm1Cba>/Des<tm1Cba>	involves: 129S2/SvPas * C57BL/6J	N	11827695
MGI:5912041	F	MP:0000274	enlarged heart	Des<tm1Cba>/Des<tm1Cba>	involves: 129S2/SvPas * C57BL/6J	N	11827695
MGI:5912041	F	MP:0005140	decreased cardiac muscle contractility	Des<tm1Cba>/Des<tm1Cba>	involves: 129S2/SvPas * C57BL/6J	N	11827695
MGI:5912041	F	MP:0003819	increased left ventricle diastolic pressure	Des<tm1Cba>/Des<tm1Cba>	involves: 129S2/SvPas * C57BL/6J	N	11827695
MGI:5912041	F	MP:0021157	increased heart left ventricle wall thickness	Des<tm1Cba>/Des<tm1Cba>	involves: 129S2/SvPas * C57BL/6J	N	11827695
MGI:5912041	F	MP:0005330	cardiomyopathy	Des<tm1Cba>/Des<tm1Cba>	involves: 129S2/SvPas * C57BL/6J	N	11827695
MGI:5912041	F	MP:0003824	decreased left ventricle developed pressure	Des<tm1Cba>/Des<tm1Cba>	involves: 129S2/SvPas * C57BL/6J	N	11827695
MGI:5912045	F	MP:0003393	decreased cardiac output	Lrig3<tm1.1Hhed>/Lrig3<tm1.1Hhed>	B6.129(Cg)-Lrig3<tm1.1Hhed>	N	27009049
MGI:5912045	M	MP:0003442	decreased circulating glycerol level	Lrig3<tm1.1Hhed>/Lrig3<tm1.1Hhed>	B6.129(Cg)-Lrig3<tm1.1Hhed>	N	27009049
MGI:5912045	F	MP:0003921	abnormal heart left ventricle morphology	Lrig3<tm1.1Hhed>/Lrig3<tm1.1Hhed>	B6.129(Cg)-Lrig3<tm1.1Hhed>	N	27009049
MGI:5912045	F	MP:0020204	abnormal heart left ventricle weight	Lrig3<tm1.1Hhed>/Lrig3<tm1.1Hhed>	B6.129(Cg)-Lrig3<tm1.1Hhed>	N	27009049
MGI:5912045	F	MP:0011952	decreased cardiac stroke volume	Lrig3<tm1.1Hhed>/Lrig3<tm1.1Hhed>	B6.129(Cg)-Lrig3<tm1.1Hhed>	N	27009049
MGI:5912045	M	MP:0002626	increased heart rate	Lrig3<tm1.1Hhed>/Lrig3<tm1.1Hhed>	B6.129(Cg)-Lrig3<tm1.1Hhed>	N	27009049
MGI:5912138	M	MP:0006321	increased myocardial fiber number	Emd<tm1.1Stw>/Y	involves: 129S1/Sv * C57BL/6	N	25274778
MGI:5912138	M	MP:0000278	abnormal myocardial fiber morphology	Emd<tm1.1Stw>/Y	involves: 129S1/Sv * C57BL/6	N	25274778
MGI:5912138	M	MP:0002833	increased heart weight	Emd<tm1.1Stw>/Y	involves: 129S1/Sv * C57BL/6	N	25274778
MGI:5912138	M	MP:0031634	decreased heart right ventricle muscle contractility	Emd<tm1.1Stw>/Y	involves: 129S1/Sv * C57BL/6	N	25274778
MGI:5912138	M	MP:0004565	decreased myocardial fiber size	Emd<tm1.1Stw>/Y	involves: 129S1/Sv * C57BL/6	N	25274778
MGI:5912138	M	MP:0005598	decreased heart ventricle muscle contractility	Emd<tm1.1Stw>/Y	involves: 129S1/Sv * C57BL/6	N	25274778
MGI:5912138	M	MP:0011925	abnormal heart echocardiography feature	Emd<tm1.1Stw>/Y	involves: 129S1/Sv * C57BL/6	N	25274778
MGI:5912138	M	MP:0031633	decreased heart left ventricle muscle contractility	Emd<tm1.1Stw>/Y	involves: 129S1/Sv * C57BL/6	N	25274778
MGI:5912138	M	MP:0004485	increased response of heart to induced stress	Emd<tm1.1Stw>/Y	involves: 129S1/Sv * C57BL/6	N	25274778
MGI:5912138	M	MP:0001544	abnormal cardiovascular system physiology	Emd<tm1.1Stw>/Y	involves: 129S1/Sv * C57BL/6	N	25274778
MGI:5912228	F	MP:0001260	increased body weight	Tg(CAG-PPARG,-tdTomato)#Sig/0,Tg(Pomc1-cre)16Lowl/0	involves: C57BL/6 * FVB/N * SJL	N	27199455
MGI:5912229	M	MP:0014170	increased brown adipose tissue mass	Tg(CAG-PPARG*,-tdTomato)#Sig/0,Tg(Pomc1-cre)16Lowl/0	involves: C57BL/6 * FVB/N * SJL	N	27199455
MGI:5912229	F	MP:0001260	increased body weight	Tg(CAG-PPARG*,-tdTomato)#Sig/0,Tg(Pomc1-cre)16Lowl/0	involves: C57BL/6 * FVB/N * SJL	N	27199455
MGI:5912229	M	MP:0001260	increased body weight	Tg(CAG-PPARG*,-tdTomato)#Sig/0,Tg(Pomc1-cre)16Lowl/0	involves: C57BL/6 * FVB/N * SJL	N	27199455
MGI:5912229	M	MP:0003961	decreased lean body mass	Tg(CAG-PPARG*,-tdTomato)#Sig/0,Tg(Pomc1-cre)16Lowl/0	involves: C57BL/6 * FVB/N * SJL	N	27199455
MGI:5912229	F	MP:0003961	decreased lean body mass	Tg(CAG-PPARG*,-tdTomato)#Sig/0,Tg(Pomc1-cre)16Lowl/0	involves: C57BL/6 * FVB/N * SJL	N	27199455
MGI:5912229	M	MP:0010934	increased subcutaneous adipose tissue amount	Tg(CAG-PPARG*,-tdTomato)#Sig/0,Tg(Pomc1-cre)16Lowl/0	involves: C57BL/6 * FVB/N * SJL	N	27199455
MGI:5912229	F	MP:0014142	increased body fat mass	Tg(CAG-PPARG*,-tdTomato)#Sig/0,Tg(Pomc1-cre)16Lowl/0	involves: C57BL/6 * FVB/N * SJL	N	27199455
MGI:5912229	M	MP:0014142	increased body fat mass	Tg(CAG-PPARG*,-tdTomato)#Sig/0,Tg(Pomc1-cre)16Lowl/0	involves: C57BL/6 * FVB/N * SJL	N	27199455
MGI:5912229	M	MP:0005375	adipose tissue phenotype	Tg(CAG-PPARG*,-tdTomato)#Sig/0,Tg(Pomc1-cre)16Lowl/0	involves: C57BL/6 * FVB/N * SJL	Y	27199455
MGI:5912229	M	MP:0001262	decreased body weight	Tg(CAG-PPARG*,-tdTomato)#Sig/0,Tg(Pomc1-cre)16Lowl/0	involves: C57BL/6 * FVB/N * SJL	N	27199455
MGI:5912243	M	MP:0020950	decreased susceptibility to Coronaviridae infection	Ace2<tm1Pngr>/Y	B6.129P2-Ace2<tm1Pngr>/J	N	16007097
MGI:5912243	M	MP:0005385	cardiovascular system phenotype	Ace2<tm1Pngr>/Y	B6.129P2-Ace2<tm1Pngr>/J	Y	17499227
MGI:5912245	M	MP:0005599	increased cardiac muscle contractility	Ace2<tm1Pngr>/Y,Pik3cg<tm1Pngr>/Pik3cg<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6	N	17499227
MGI:5912281	F	MP:0009356	decreased liver triglyceride level	Hkdc1<tm1a(KOMP)Wtsi>/Hkdc1<+>	involves: C57BL/6N	N	27459389
MGI:5925277	M	MP:0001925	male infertility	Clcn2<nmf289>/Clcn2<nmf289>	CByJ.Cg-Clcn2<nmf289>/Pjn	N	28859131
MGI:5925277	M	MP:0005159	azoospermia	Clcn2<nmf289>/Clcn2<nmf289>	CByJ.Cg-Clcn2<nmf289>/Pjn	N	28859131
MGI:5925307	M	MP:0009278	abnormal bone marrow cell physiology	Bcor<tm1.1Vjba>/Y	involves: 129S1/Sv	N	26847029
MGI:5925307	M	MP:0000351	increased cell proliferation	Bcor<tm1.1Vjba>/Y	involves: 129S1/Sv	N	26847029
MGI:5925308	M	MP:0000219	increased neutrophil cell number	Bcor<tm1.1Vjba>/Y,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	involves: 129S1/Sv * C57BL/6 * CBA/Ca	N	26847029
MGI:5925391	M	MP:0002083	premature death	Cdc73<Gt(RRE190)Byg>/Cdc73<+>	B6.129P2-Cdc73<Gt(RRE190)Byg>	N	28288139
MGI:5925391	F	MP:0009222	increased uterus tumor incidence	Cdc73<Gt(RRE190)Byg>/Cdc73<+>	B6.129P2-Cdc73<Gt(RRE190)Byg>	N	28288139
MGI:5925391	F	MP:0009092	endometrium hyperplasia	Cdc73<Gt(RRE190)Byg>/Cdc73<+>	B6.129P2-Cdc73<Gt(RRE190)Byg>	N	28288139
MGI:5925391	F	MP:0009082	uterus cyst	Cdc73<Gt(RRE190)Byg>/Cdc73<+>	B6.129P2-Cdc73<Gt(RRE190)Byg>	N	28288139
MGI:5925391	F	MP:0008256	abnormal myometrium morphology	Cdc73<Gt(RRE190)Byg>/Cdc73<+>	B6.129P2-Cdc73<Gt(RRE190)Byg>	N	28288139
MGI:6093470	F	MP:0001272	increased metastatic potential	Ccn6<tm1.1Cgkl>/Ccn6<tm1.1Cgkl>,Tg(MMTV-cre)1Mam/0	FVB/N-Ccn6<tm1.1Cgkl> Tg(MMTV-cre)1Mam	N	27819674
MGI:6093470	F	MP:0001883	increased mammary adenocarcinoma incidence	Ccn6<tm1.1Cgkl>/Ccn6<tm1.1Cgkl>,Tg(MMTV-cre)1Mam/0	FVB/N-Ccn6<tm1.1Cgkl> Tg(MMTV-cre)1Mam	N	27819674
MGI:6093470	F	MP:0000627	abnormal mammary gland morphology	Ccn6<tm1.1Cgkl>/Ccn6<tm1.1Cgkl>,Tg(MMTV-cre)1Mam/0	FVB/N-Ccn6<tm1.1Cgkl> Tg(MMTV-cre)1Mam	N	27819674
MGI:6093470	F	MP:0001885	mammary gland duct hyperplasia	Ccn6<tm1.1Cgkl>/Ccn6<tm1.1Cgkl>,Tg(MMTV-cre)1Mam/0	FVB/N-Ccn6<tm1.1Cgkl> Tg(MMTV-cre)1Mam	N	27819674
MGI:6093470	F	MP:0013782	abnormal mammary duct terminal end bud morphology	Ccn6<tm1.1Cgkl>/Ccn6<tm1.1Cgkl>,Tg(MMTV-cre)1Mam/0	FVB/N-Ccn6<tm1.1Cgkl> Tg(MMTV-cre)1Mam	N	27819674
MGI:6093470	F	MP:0009503	abnormal mammary gland duct morphology	Ccn6<tm1.1Cgkl>/Ccn6<tm1.1Cgkl>,Tg(MMTV-cre)1Mam/0	FVB/N-Ccn6<tm1.1Cgkl> Tg(MMTV-cre)1Mam	N	27819674
MGI:6093470	F	MP:0006271	abnormal involution of the mammary gland	Ccn6<tm1.1Cgkl>/Ccn6<tm1.1Cgkl>,Tg(MMTV-cre)1Mam/0	FVB/N-Ccn6<tm1.1Cgkl> Tg(MMTV-cre)1Mam	N	27819674
MGI:6093471	F	MP:0001272	increased metastatic potential	Ccn6<tm1.1Cgkl>/Ccn6<tm1.1Cgkl>,Tg(MMTV-cre)1Mam/0,Tg(MMTV-PyVT)634Mul/0	FVB/N-Ccn6<tm1.1Cgkl> Tg(MMTV-cre)1Mam Tg(MMTV-PyVT)634Mul	N	27819674
MGI:6093471	F	MP:0001883	increased mammary adenocarcinoma incidence	Ccn6<tm1.1Cgkl>/Ccn6<tm1.1Cgkl>,Tg(MMTV-cre)1Mam/0,Tg(MMTV-PyVT)634Mul/0	FVB/N-Ccn6<tm1.1Cgkl> Tg(MMTV-cre)1Mam Tg(MMTV-PyVT)634Mul	N	27819674
MGI:6093700	F	MP:0001273	decreased metastatic potential	Tgfb1i1<tm1.2Cet>/Tgfb1i1<tm1.2Cet>,Tg(MMTV-PyVT)634Mul/0	involves: 129S/SvEv * C57BL/6 * FVB/N	N	27893716
MGI:6093700	F	MP:0010269	decreased mammary gland tumor incidence	Tgfb1i1<tm1.2Cet>/Tgfb1i1<tm1.2Cet>,Tg(MMTV-PyVT)634Mul/0	involves: 129S/SvEv * C57BL/6 * FVB/N	N	27893716
MGI:6093705	M	MP:0001922	reduced male fertility	Rfwd3<tm1.1Dtch>/Rfwd3<tm1.1Dtch>	involves: C57BL/6	N	28691929
MGI:6093705	F	MP:0001127	small ovary	Rfwd3<tm1.1Dtch>/Rfwd3<tm1.1Dtch>	involves: C57BL/6	N	28691929
MGI:6093705	M	MP:0003205	testicular atrophy	Rfwd3<tm1.1Dtch>/Rfwd3<tm1.1Dtch>	involves: C57BL/6	N	28691929
MGI:6093705	M	MP:0002687	oligozoospermia	Rfwd3<tm1.1Dtch>/Rfwd3<tm1.1Dtch>	involves: C57BL/6	N	28691929
MGI:6093705	F	MP:0004833	ovary atrophy	Rfwd3<tm1.1Dtch>/Rfwd3<tm1.1Dtch>	involves: C57BL/6	N	28691929
MGI:6093705	F	MP:0001923	reduced female fertility	Rfwd3<tm1.1Dtch>/Rfwd3<tm1.1Dtch>	involves: C57BL/6	N	28691929
MGI:6093705	F	MP:0001129	impaired ovarian folliculogenesis	Rfwd3<tm1.1Dtch>/Rfwd3<tm1.1Dtch>	involves: C57BL/6	N	28691929
MGI:6093712	M	MP:0001147	small testis	Spata2<em1Jliu>/Spata2<em1Jliu>	involves: ICR	N	29025062
MGI:6093712	M	MP:0002675	asthenozoospermia	Spata2<em1Jliu>/Spata2<em1Jliu>	involves: ICR	N	29025062
MGI:6093712	M	MP:0006378	abnormal spermatogonia morphology	Spata2<em1Jliu>/Spata2<em1Jliu>	involves: ICR	N	29025062
MGI:6093712	M	MP:0004901	decreased male germ cell number	Spata2<em1Jliu>/Spata2<em1Jliu>	involves: ICR	N	29025062
MGI:6093712	M	MP:0001153	small seminiferous tubules	Spata2<em1Jliu>/Spata2<em1Jliu>	involves: ICR	N	29025062
MGI:6093712	M	MP:0002687	oligozoospermia	Spata2<em1Jliu>/Spata2<em1Jliu>	involves: ICR	N	29025062
MGI:6093712	M	MP:0009647	decreased fertilization frequency	Spata2<em1Jliu>/Spata2<em1Jliu>	involves: ICR	N	29025062
MGI:6093712	M	MP:0004852	decreased testis weight	Spata2<em1Jliu>/Spata2<em1Jliu>	involves: ICR	N	29025062
MGI:6093712	M	MP:0001922	reduced male fertility	Spata2<em1Jliu>/Spata2<em1Jliu>	involves: ICR	N	29025062
MGI:6093713	M	MP:0002286	cryptorchism	Lifr<tm1Imx>/Lifr<tm1Imx>	B6;129S7-Lifr<tm1Imx>/J	N	28334964
MGI:6094191	M	MP:0002083	premature death	Cd1d1<tm1Luc>/Cd1d1<tm1Luc>,X/Yaa	BXSB.129S6(B6)-Cd1d1<tm1Luc>/Dcr	N	21964024
MGI:6094201	M	MP:0002083	premature death	B2m<tm1Unc>/B2m<tm1Unc>,X/Yaa	BXSB.129P2(B6)-B2m<tm1Unc>/Dcr	N	21964024
MGI:6094201	M	MP:0004801	increased susceptibility to systemic lupus erythematosus	B2m<tm1Unc>/B2m<tm1Unc>,X/Yaa	BXSB.129P2(B6)-B2m<tm1Unc>/Dcr	N	21964024
MGI:6094201	M	MP:0004794	increased anti-nuclear antigen antibody level	B2m<tm1Unc>/B2m<tm1Unc>,X/Yaa	BXSB.129P2(B6)-B2m<tm1Unc>/Dcr	N	21964024
MGI:6094214	M	MP:0002286	cryptorchism	Lifr<tm1Imx>/Lifr<+>	B6;129S7-Lifr<tm1Imx>/J	N	28334964
MGI:6094246	M	MP:0002083	premature death	Fcgrt<tm1Dcr>/Fcgrt<tm1Dcr>,X/Yaa	BXSB.129X1-Fcgrt<tm1Dcr>/Dcr	N	21964024
MGI:6094247	M	MP:0002083	premature death	H2-D1<b-tm1Bpe>/H2-D1<b-tm1Bpe>,H2-K1<b-tm1Bpe>/H2-K1<b-tm1Bpe>,X/Yaa	BXSB.129P2(B6)-H2-K1<b-tm1Bpe> H2-D1<b-tm1Bpe>/Dcr	N	21964024
MGI:6094247	M	MP:0004801	increased susceptibility to systemic lupus erythematosus	H2-D1<b-tm1Bpe>/H2-D1<b-tm1Bpe>,H2-K1<b-tm1Bpe>/H2-K1<b-tm1Bpe>,X/Yaa	BXSB.129P2(B6)-H2-K1<b-tm1Bpe> H2-D1<b-tm1Bpe>/Dcr	N	21964024
MGI:6094248	M	MP:0004801	increased susceptibility to systemic lupus erythematosus	Tap1<tm1Arp>/Tap1<tm1Arp>,X/Yaa	BXSB.129S2(B6)-Tap1<tm1Arp>/Dcr	N	21964024
MGI:6095163	M	MP:0001925	male infertility	Rplp1<tm1.1Melt>/Rplp1<tm1.2Melt>	Not Specified	N	24959908
MGI:6098717	M	MP:0001363	increased anxiety-related response	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	B6N.129P2-Crtc1<Gt(XK522)Byg>	N	22592058
MGI:6098717	M	MP:0009456	impaired cued conditioning behavior	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	B6N.129P2-Crtc1<Gt(XK522)Byg>	N	22592058
MGI:6098717	M	MP:0002573	behavioral despair	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	B6N.129P2-Crtc1<Gt(XK522)Byg>	N	22592058
MGI:6098717	M	MP:0010070	decreased serotonin level	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	B6N.129P2-Crtc1<Gt(XK522)Byg>	N	22592058
MGI:6098717	M	MP:0002566	abnormal sexual interaction	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	B6N.129P2-Crtc1<Gt(XK522)Byg>	N	22592058
MGI:6098717	M	MP:0001360	abnormal social investigation	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	B6N.129P2-Crtc1<Gt(XK522)Byg>	N	22592058
MGI:6098717	M	MP:0001447	abnormal nest building behavior	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	B6N.129P2-Crtc1<Gt(XK522)Byg>	N	22592058
MGI:6098717	M	MP:0009710	anhedonia	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	B6N.129P2-Crtc1<Gt(XK522)Byg>	N	22592058
MGI:6098717	F	MP:0001356	increased aggression towards female mice	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	B6N.129P2-Crtc1<Gt(XK522)Byg>	N	22592058
MGI:6098717	M	MP:0001354	increased aggression towards male mice	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	B6N.129P2-Crtc1<Gt(XK522)Byg>	N	22592058
MGI:6098717	M	MP:0001764	abnormal homeostasis	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	B6N.129P2-Crtc1<Gt(XK522)Byg>	N	22592058
MGI:6098717	M	MP:0001417	decreased exploration in new environment	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	B6N.129P2-Crtc1<Gt(XK522)Byg>	N	22592058
MGI:6098717	M	MP:0001361	social withdrawal	Crtc1<Gt(XK522)Byg>/Crtc1<Gt(XK522)Byg>	B6N.129P2-Crtc1<Gt(XK522)Byg>	N	22592058
MGI:6098752	M	MP:0001636	irregular heartbeat	Mecp2<tm1.1Bird>/Y	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098752	M	MP:0006277	abnormal parasympathetic nervous system physiology	Mecp2<tm1.1Bird>/Y	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098752	M	MP:0009732	ventricular premature beat	Mecp2<tm1.1Bird>/Y	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098752	M	MP:0005534	decreased body temperature	Mecp2<tm1.1Bird>/Y	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098752	M	MP:0001402	decreased locomotor activity	Mecp2<tm1.1Bird>/Y	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098752	M	MP:0003928	increased heart rate variability	Mecp2<tm1.1Bird>/Y	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098752	M	MP:0004183	abnormal sympathetic nervous system physiology	Mecp2<tm1.1Bird>/Y	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098752	M	MP:0005333	decreased heart rate	Mecp2<tm1.1Bird>/Y	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098752	M	MP:0010519	atrioventricular block	Mecp2<tm1.1Bird>/Y	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098753	F	MP:0010519	atrioventricular block	Mecp2<tm1.1Bird>/Mecp2<+>	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098753	F	MP:0005386	behavior/neurological phenotype	Mecp2<tm1.1Bird>/Mecp2<+>	B6.129P2(C)-Mecp2<tm1.1Bird>/J	Y	28159985
MGI:6098753	F	MP:0009732	ventricular premature beat	Mecp2<tm1.1Bird>/Mecp2<+>	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098753	F	MP:0005333	decreased heart rate	Mecp2<tm1.1Bird>/Mecp2<+>	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098753	F	MP:0003928	increased heart rate variability	Mecp2<tm1.1Bird>/Mecp2<+>	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098753	F	MP:0001636	irregular heartbeat	Mecp2<tm1.1Bird>/Mecp2<+>	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098753	F	MP:0001629	abnormal heart rate	Mecp2<tm1.1Bird>/Mecp2<+>	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098753	F	MP:0005534	decreased body temperature	Mecp2<tm1.1Bird>/Mecp2<+>	B6.129P2(C)-Mecp2<tm1.1Bird>/J	N	28159985
MGI:6098754	M	MP:0001629	abnormal heart rate	Mecp2<tm2Bird>/Y	B6.129P2-Mecp2<tm2Bird>/J	N	28159985
MGI:6098754	M	MP:0005534	decreased body temperature	Mecp2<tm2Bird>/Y	B6.129P2-Mecp2<tm2Bird>/J	N	28159985
MGI:6098754	M	MP:0010519	atrioventricular block	Mecp2<tm2Bird>/Y	B6.129P2-Mecp2<tm2Bird>/J	N	28159985
MGI:6098754	M	MP:0001943	abnormal respiration	Mecp2<tm2Bird>/Y	B6.129P2-Mecp2<tm2Bird>/J	N	28159985
MGI:6098754	M	MP:0003233	prolonged QT interval	Mecp2<tm2Bird>/Y	B6.129P2-Mecp2<tm2Bird>/J	N	28159985
MGI:6098754	M	MP:0005333	decreased heart rate	Mecp2<tm2Bird>/Y	B6.129P2-Mecp2<tm2Bird>/J	N	28159985
MGI:6098754	M	MP:0001957	apnea	Mecp2<tm2Bird>/Y	B6.129P2-Mecp2<tm2Bird>/J	N	28159985
MGI:6098754	M	MP:0004085	abnormal heartbeat	Mecp2<tm2Bird>/Y	B6.129P2-Mecp2<tm2Bird>/J	N	28159985
MGI:6098754	M	MP:0002083	premature death	Mecp2<tm2Bird>/Y	B6.129P2-Mecp2<tm2Bird>/J	N	28159985
MGI:6098754	M	MP:0004485	increased response of heart to induced stress	Mecp2<tm2Bird>/Y	B6.129P2-Mecp2<tm2Bird>/J	N	28159985
MGI:6098754	M	MP:0009732	ventricular premature beat	Mecp2<tm2Bird>/Y	B6.129P2-Mecp2<tm2Bird>/J	N	28159985
MGI:6098754	M	MP:0003928	increased heart rate variability	Mecp2<tm2Bird>/Y	B6.129P2-Mecp2<tm2Bird>/J	N	28159985
MGI:6098756	M	MP:0005333	decreased heart rate	Mecp2<tm1Jae>/Y,Chat<tm2(cre)Lowl>/Chat<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	28159985
MGI:6098756	M	MP:0004485	increased response of heart to induced stress	Mecp2<tm1Jae>/Y,Chat<tm2(cre)Lowl>/Chat<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	28159985
MGI:6098756	M	MP:0004085	abnormal heartbeat	Mecp2<tm1Jae>/Y,Chat<tm2(cre)Lowl>/Chat<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	28159985
MGI:6098756	M	MP:0005388	respiratory system phenotype	Mecp2<tm1Jae>/Y,Chat<tm2(cre)Lowl>/Chat<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J	Y	28159985
MGI:6098756	M	MP:0002083	premature death	Mecp2<tm1Jae>/Y,Chat<tm2(cre)Lowl>/Chat<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	28159985
MGI:6098756	M	MP:0005534	decreased body temperature	Mecp2<tm1Jae>/Y,Chat<tm2(cre)Lowl>/Chat<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	28159985
MGI:6098756	M	MP:0009732	ventricular premature beat	Mecp2<tm1Jae>/Y,Chat<tm2(cre)Lowl>/Chat<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	28159985
MGI:6098756	M	MP:0003928	increased heart rate variability	Mecp2<tm1Jae>/Y,Chat<tm2(cre)Lowl>/Chat<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	28159985
MGI:6098756	M	MP:0008950	ventricular tachycardia	Mecp2<tm1Jae>/Y,Chat<tm2(cre)Lowl>/Chat<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	28159985
MGI:6098756	M	MP:0005386	behavior/neurological phenotype	Mecp2<tm1Jae>/Y,Chat<tm2(cre)Lowl>/Chat<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J	Y	28159985
MGI:6098756	M	MP:0003233	prolonged QT interval	Mecp2<tm1Jae>/Y,Chat<tm2(cre)Lowl>/Chat<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	28159985
MGI:6098758	M	MP:0005386	behavior/neurological phenotype	Mecp2<tm1Jae>/Y,Tg(Myh6-cre)2182Mds/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * FVB/N	Y	28159985
MGI:6098758	M	MP:0005385	cardiovascular system phenotype	Mecp2<tm1Jae>/Y,Tg(Myh6-cre)2182Mds/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * FVB/N	Y	28159985
MGI:6098758	M	MP:0005376	homeostasis/metabolism phenotype	Mecp2<tm1Jae>/Y,Tg(Myh6-cre)2182Mds/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * FVB/N	Y	28159985
MGI:6098759	M	MP:0001943	abnormal respiration	Chat<tm2(cre)Lowl>/Chat<+>,Mecp2<tm2Bird>/Y	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J	N	28159985
MGI:6098759	M	MP:0005386	behavior/neurological phenotype	Chat<tm2(cre)Lowl>/Chat<+>,Mecp2<tm2Bird>/Y	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J	Y	28159985
MGI:6098759	M	MP:0005385	cardiovascular system phenotype	Chat<tm2(cre)Lowl>/Chat<+>,Mecp2<tm2Bird>/Y	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J	Y	28159985
MGI:6098759	M	MP:0001957	apnea	Chat<tm2(cre)Lowl>/Chat<+>,Mecp2<tm2Bird>/Y	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J	N	28159985
MGI:6098759	M	MP:0005376	homeostasis/metabolism phenotype	Chat<tm2(cre)Lowl>/Chat<+>,Mecp2<tm2Bird>/Y	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J	Y	28159985
MGI:6099040	M	MP:0004777	abnormal phospholipid level	Agpat3<tm1a(EUCOMM)Wtsi>/Agpat3<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	28578315
MGI:6099040	M	MP:0005578	teratozoospermia	Agpat3<tm1a(EUCOMM)Wtsi>/Agpat3<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	28578315
MGI:6099040	M	MP:0001925	male infertility	Agpat3<tm1a(EUCOMM)Wtsi>/Agpat3<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	28578315
MGI:6099040	M	MP:0000242	impaired fertilization	Agpat3<tm1a(EUCOMM)Wtsi>/Agpat3<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	28578315
MGI:6099040	M	MP:0002687	oligozoospermia	Agpat3<tm1a(EUCOMM)Wtsi>/Agpat3<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	28578315
MGI:6099040	M	MP:0002784	abnormal Sertoli cell morphology	Agpat3<tm1a(EUCOMM)Wtsi>/Agpat3<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	28578315
MGI:6099040	M	MP:0009230	abnormal sperm head morphology	Agpat3<tm1a(EUCOMM)Wtsi>/Agpat3<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	28578315
MGI:6099056	M	MP:0005643	decreased dopamine level	Tg(Th-SNCA)5Eric/0	involves: C57BL/6 * C57BL/6J	N	15009131
MGI:6099056	M	MP:0003244	loss of dopaminergic neurons	Tg(Th-SNCA)5Eric/0	involves: C57BL/6 * C57BL/6J	N	15009131
MGI:6099056	M	MP:0011449	increased dopaminergic neuron number	Tg(Th-SNCA)5Eric/0	involves: C57BL/6 * C57BL/6J	N	15009131
MGI:6099056	M	MP:0001402	decreased locomotor activity	Tg(Th-SNCA)5Eric/0	involves: C57BL/6 * C57BL/6J	N	15009131
MGI:6099056	M	MP:0008873	increased physiological sensitivity to xenobiotic	Tg(Th-SNCA)5Eric/0	involves: C57BL/6 * C57BL/6J	N	15009131
MGI:6099058	M	MP:0001402	decreased locomotor activity	Tg(Th-SNCA*A30P*A53T)39Eric/0	involves: C57BL/6 * C57BL/6J	N	15009131
MGI:6099058	M	MP:0008873	increased physiological sensitivity to xenobiotic	Tg(Th-SNCA*A30P*A53T)39Eric/0	involves: C57BL/6 * C57BL/6J	N	15009131
MGI:6099058	M	MP:0005643	decreased dopamine level	Tg(Th-SNCA*A30P*A53T)39Eric/0	involves: C57BL/6 * C57BL/6J	N	15009131
MGI:6099058	M	MP:0003244	loss of dopaminergic neurons	Tg(Th-SNCA*A30P*A53T)39Eric/0	involves: C57BL/6 * C57BL/6J	N	15009131
MGI:6101187	F	MP:0002083	premature death	Tg(C9orf72)500Lpwr/0	FVB/NJ-Tg(C9orf72)500Lpwr	N	27112499
MGI:6103875	M	MP:0012606	increased glutathione level	G6pdx<a-m1Neu>/Y,Tg(Myh6-CRYAB*R120G)7302Ijb/0	involves: 102/El * C3H/El * C57BL/6	N	17693254
MGI:6103875	M	MP:0005385	cardiovascular system phenotype	G6pdx<a-m1Neu>/Y,Tg(Myh6-CRYAB*R120G)7302Ijb/0	involves: 102/El * C3H/El * C57BL/6	Y	17693254
MGI:6103876	F	MP:0008000	increased ovary tumor incidence	Fancf<tm1Nki>/Fancf<tm1Nki>	involves: 129P2/OlaHsd * FVB	N	21915857
MGI:6103876	F	MP:0001127	small ovary	Fancf<tm1Nki>/Fancf<tm1Nki>	involves: 129P2/OlaHsd * FVB	N	21915857
MGI:6103876	F	MP:0001751	increased circulating luteinizing hormone level	Fancf<tm1Nki>/Fancf<tm1Nki>	involves: 129P2/OlaHsd * FVB	N	21915857
MGI:6103876	F	MP:0001927	abnormal estrous cycle	Fancf<tm1Nki>/Fancf<tm1Nki>	involves: 129P2/OlaHsd * FVB	N	21915857
MGI:6103876	F	MP:0010383	increased adenoma incidence	Fancf<tm1Nki>/Fancf<tm1Nki>	involves: 129P2/OlaHsd * FVB	N	21915857
MGI:6103876	F	MP:0012411	increased granulosa cell tumor incidence	Fancf<tm1Nki>/Fancf<tm1Nki>	involves: 129P2/OlaHsd * FVB	N	21915857
MGI:6103876	F	MP:0001750	increased circulating follicle stimulating hormone level	Fancf<tm1Nki>/Fancf<tm1Nki>	involves: 129P2/OlaHsd * FVB	N	21915857
MGI:6103876	M	MP:0005159	azoospermia	Fancf<tm1Nki>/Fancf<tm1Nki>	involves: 129P2/OlaHsd * FVB	N	21915857
MGI:6103876	F	MP:0011121	decreased primordial ovarian follicle number	Fancf<tm1Nki>/Fancf<tm1Nki>	involves: 129P2/OlaHsd * FVB	N	21915857
MGI:6103876	F	MP:0008871	abnormal ovarian follicle number	Fancf<tm1Nki>/Fancf<tm1Nki>	involves: 129P2/OlaHsd * FVB	N	21915857
MGI:6103903	F	MP:0011049	impaired adaptive thermogenesis	Lcn2<tm1Aade>/Lcn2<tm1Aade>	B6.129P2-Lcn2<tm1Aade>	N	20332347
MGI:6104236	M	MP:0002083	premature death	Cd8a<tm1Mak>/Cd8a<tm1Mak>,X/Yaa	BXSB.129S2(B6)-Cd8a<tm1Mak>/4Dcr	N	21964024
MGI:6104236	M	MP:0004801	increased susceptibility to systemic lupus erythematosus	Cd8a<tm1Mak>/Cd8a<tm1Mak>,X/Yaa	BXSB.129S2(B6)-Cd8a<tm1Mak>/4Dcr	N	21964024
MGI:6104239	M	MP:0002662	abnormal cauda epididymis morphology	Cfap157<tm1d(EUCOMM)Hmgu>/Cfap157<tm1d(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104239	M	MP:0008892	abnormal sperm flagellum morphology	Cfap157<tm1d(EUCOMM)Hmgu>/Cfap157<tm1d(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104239	M	MP:0009234	absent sperm head	Cfap157<tm1d(EUCOMM)Hmgu>/Cfap157<tm1d(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104239	M	MP:0000358	abnormal cell morphology	Cfap157<tm1d(EUCOMM)Hmgu>/Cfap157<tm1d(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104239	M	MP:0002674	abnormal sperm motility	Cfap157<tm1d(EUCOMM)Hmgu>/Cfap157<tm1d(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104239	M	MP:0009831	abnormal sperm midpiece morphology	Cfap157<tm1d(EUCOMM)Hmgu>/Cfap157<tm1d(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104239	M	MP:0009230	abnormal sperm head morphology	Cfap157<tm1d(EUCOMM)Hmgu>/Cfap157<tm1d(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104239	M	MP:0009282	decreased hyperactivated sperm motility	Cfap157<tm1d(EUCOMM)Hmgu>/Cfap157<tm1d(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104239	M	MP:0001925	male infertility	Cfap157<tm1d(EUCOMM)Hmgu>/Cfap157<tm1d(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104239	M	MP:0004901	decreased male germ cell number	Cfap157<tm1d(EUCOMM)Hmgu>/Cfap157<tm1d(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104240	M	MP:0008892	abnormal sperm flagellum morphology	Cfap157<tm1b(EUCOMM)Hmgu>/Cfap157<tm1b(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104240	M	MP:0009831	abnormal sperm midpiece morphology	Cfap157<tm1b(EUCOMM)Hmgu>/Cfap157<tm1b(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104240	M	MP:0000358	abnormal cell morphology	Cfap157<tm1b(EUCOMM)Hmgu>/Cfap157<tm1b(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104240	M	MP:0002674	abnormal sperm motility	Cfap157<tm1b(EUCOMM)Hmgu>/Cfap157<tm1b(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104240	M	MP:0009230	abnormal sperm head morphology	Cfap157<tm1b(EUCOMM)Hmgu>/Cfap157<tm1b(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104240	M	MP:0009234	absent sperm head	Cfap157<tm1b(EUCOMM)Hmgu>/Cfap157<tm1b(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104240	M	MP:0001925	male infertility	Cfap157<tm1b(EUCOMM)Hmgu>/Cfap157<tm1b(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104240	M	MP:0002662	abnormal cauda epididymis morphology	Cfap157<tm1b(EUCOMM)Hmgu>/Cfap157<tm1b(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104240	M	MP:0009282	decreased hyperactivated sperm motility	Cfap157<tm1b(EUCOMM)Hmgu>/Cfap157<tm1b(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6104240	M	MP:0004901	decreased male germ cell number	Cfap157<tm1b(EUCOMM)Hmgu>/Cfap157<tm1b(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	27965440
MGI:6105930	M	MP:0002083	premature death	Il15<tm1Imx>/Il15<tm1Imx>,X/Yaa	BXSB.B6-Il15<tm1Imx>/Dcr	N	21964024
MGI:6105930	M	MP:0004801	increased susceptibility to systemic lupus erythematosus	Il15<tm1Imx>/Il15<tm1Imx>,X/Yaa	BXSB.B6-Il15<tm1Imx>/Dcr	N	21964024
MGI:6105946	M	MP:0004794	increased anti-nuclear antigen antibody level	Cd8a<tm1Mak>/Cd8a<tm1Mak>,Il15<tm1Imx>/Il15<tm1Imx>,X/Yaa	BXSB.Cg-Cd8a<tm1Mak> Il15<tm1Imx>/Dcr	N	21964024
MGI:6105946	M	MP:0008470	abnormal spleen B cell follicle morphology	Cd8a<tm1Mak>/Cd8a<tm1Mak>,Il15<tm1Imx>/Il15<tm1Imx>,X/Yaa	BXSB.Cg-Cd8a<tm1Mak> Il15<tm1Imx>/Dcr	N	21964024
MGI:6105946	M	MP:0002083	premature death	Cd8a<tm1Mak>/Cd8a<tm1Mak>,Il15<tm1Imx>/Il15<tm1Imx>,X/Yaa	BXSB.Cg-Cd8a<tm1Mak> Il15<tm1Imx>/Dcr	N	21964024
MGI:6105946	M	MP:0020519	renal glomerular immunoglobulin deposits	Cd8a<tm1Mak>/Cd8a<tm1Mak>,Il15<tm1Imx>/Il15<tm1Imx>,X/Yaa	BXSB.Cg-Cd8a<tm1Mak> Il15<tm1Imx>/Dcr	N	21964024
MGI:6105946	M	MP:0004801	increased susceptibility to systemic lupus erythematosus	Cd8a<tm1Mak>/Cd8a<tm1Mak>,Il15<tm1Imx>/Il15<tm1Imx>,X/Yaa	BXSB.Cg-Cd8a<tm1Mak> Il15<tm1Imx>/Dcr	N	21964024
MGI:6105946	M	MP:0000220	increased monocyte cell number	Cd8a<tm1Mak>/Cd8a<tm1Mak>,Il15<tm1Imx>/Il15<tm1Imx>,X/Yaa	BXSB.Cg-Cd8a<tm1Mak> Il15<tm1Imx>/Dcr	N	21964024
MGI:6105946	M	MP:0008501	increased IgG2b level	Cd8a<tm1Mak>/Cd8a<tm1Mak>,Il15<tm1Imx>/Il15<tm1Imx>,X/Yaa	BXSB.Cg-Cd8a<tm1Mak> Il15<tm1Imx>/Dcr	N	21964024
MGI:6105946	M	MP:0008500	increased IgG2a level	Cd8a<tm1Mak>/Cd8a<tm1Mak>,Il15<tm1Imx>/Il15<tm1Imx>,X/Yaa	BXSB.Cg-Cd8a<tm1Mak> Il15<tm1Imx>/Dcr	N	21964024
MGI:6105946	M	MP:0008499	increased IgG1 level	Cd8a<tm1Mak>/Cd8a<tm1Mak>,Il15<tm1Imx>/Il15<tm1Imx>,X/Yaa	BXSB.Cg-Cd8a<tm1Mak> Il15<tm1Imx>/Dcr	N	21964024
MGI:6105946	M	MP:0009338	increased splenocyte number	Cd8a<tm1Mak>/Cd8a<tm1Mak>,Il15<tm1Imx>/Il15<tm1Imx>,X/Yaa	BXSB.Cg-Cd8a<tm1Mak> Il15<tm1Imx>/Dcr	N	21964024
MGI:6105947	M	MP:0001785	edema	Tg(Myh6-Gnaq*Q209L/Esr1*)7Rzl/0	involves: C57BL/6	N	16210321
MGI:6105950	M	MP:0001844	autoimmune response	Prf1<tm1Sdz>/Prf1<tm1Sdz>,X/Yaa	BXSB.B6-Prf1<tm1Sdz>/Dcr	N	21964024
MGI:6105950	M	MP:0002083	premature death	Prf1<tm1Sdz>/Prf1<tm1Sdz>,X/Yaa	BXSB.B6-Prf1<tm1Sdz>/Dcr	N	21964024
MGI:6106900	F	MP:0010359	increased liver free fatty acids level	Nus1<tm1.1Qrm>/Nus1<tm1.1Qrm>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129 * C57BL/6 * DBA * SJL	N	27480224
MGI:6106900	F	MP:0001554	increased circulating free fatty acids level	Nus1<tm1.1Qrm>/Nus1<tm1.1Qrm>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129 * C57BL/6 * DBA * SJL	N	27480224
MGI:6106900	F	MP:0010026	decreased liver cholesterol level	Nus1<tm1.1Qrm>/Nus1<tm1.1Qrm>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129 * C57BL/6 * DBA * SJL	N	27480224
MGI:6106900	F	MP:0001552	increased circulating triglyceride level	Nus1<tm1.1Qrm>/Nus1<tm1.1Qrm>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129 * C57BL/6 * DBA * SJL	N	27480224
MGI:6106900	F	MP:0002118	abnormal lipid homeostasis	Nus1<tm1.1Qrm>/Nus1<tm1.1Qrm>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129 * C57BL/6 * DBA * SJL	N	27480224
MGI:6106900	F	MP:0000180	abnormal circulating cholesterol level	Nus1<tm1.1Qrm>/Nus1<tm1.1Qrm>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129 * C57BL/6 * DBA * SJL	N	27480224
MGI:6106900	F	MP:0009355	increased liver triglyceride level	Nus1<tm1.1Qrm>/Nus1<tm1.1Qrm>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129 * C57BL/6 * DBA * SJL	N	27480224
MGI:6106901	F	MP:0010027	increased liver cholesterol level	Nr1h3<tm1Djm>/Nr1h3<tm1Djm>,Nus1<tm1.1Qrm>/Nus1<tm1.1Qrm>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129 * C57BL/6 * DBA * SJL	N	27480224
MGI:6106901	F	MP:0005376	homeostasis/metabolism phenotype	Nr1h3<tm1Djm>/Nr1h3<tm1Djm>,Nus1<tm1.1Qrm>/Nus1<tm1.1Qrm>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: 129 * C57BL/6 * DBA * SJL	Y	27480224
MGI:6106902	F	MP:0010359	increased liver free fatty acids level	Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>,Nus1<tm1.1Qrm>/Nus1<tm1.1Qrm>	involves: 129 * C57BL/6 * SJL	N	27480224
MGI:6106902	F	MP:0002628	hepatic steatosis	Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>,Nus1<tm1.1Qrm>/Nus1<tm1.1Qrm>	involves: 129 * C57BL/6 * SJL	N	27480224
MGI:6106902	F	MP:0002118	abnormal lipid homeostasis	Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>,Nus1<tm1.1Qrm>/Nus1<tm1.1Qrm>	involves: 129 * C57BL/6 * SJL	N	27480224
MGI:6106902	F	MP:0009355	increased liver triglyceride level	Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>,Nus1<tm1.1Qrm>/Nus1<tm1.1Qrm>	involves: 129 * C57BL/6 * SJL	N	27480224
MGI:6107168	M	MP:0004802	decreased susceptibility to systemic lupus erythematosus	Ighm<tm1Cgn>/Ighm<tm1Cgn>,X/Yaa	BXSB.129S2(B6)-Ighm<tm1Cgn>/Dcr	N	24078696
MGI:6107177	M	MP:0009142	decreased prepulse inhibition	Cdr1os<em1Nikr>/Y	C57BL/6N-Cdr1os<em1Nikr>	N	28798046
MGI:6107177	M	MP:0005402	abnormal action potential	Cdr1os<em1Nikr>/Y	C57BL/6N-Cdr1os<em1Nikr>	N	28798046
MGI:6107177	M	MP:0014375	increased miniature excitatory postsynaptic current frequency	Cdr1os<em1Nikr>/Y	C57BL/6N-Cdr1os<em1Nikr>	N	28798046
MGI:6107551	M	MP:0005390	skeleton phenotype	Ostf1<tm1(NCOM)Cmhd>/Ostf1<tm1(NCOM)Cmhd>	C57BL/6-Ostf1<tm1(NCOM)Cmhd>	Y	28936620
MGI:6107551	M	MP:0013615	increased volumetric bone mineral density	Ostf1<tm1(NCOM)Cmhd>/Ostf1<tm1(NCOM)Cmhd>	C57BL/6-Ostf1<tm1(NCOM)Cmhd>	N	28936620
MGI:6107551	M	MP:0005386	behavior/neurological phenotype	Ostf1<tm1(NCOM)Cmhd>/Ostf1<tm1(NCOM)Cmhd>	C57BL/6-Ostf1<tm1(NCOM)Cmhd>	Y	28936620
MGI:6107551	M	MP:0020011	increased bone mineral density of femur	Ostf1<tm1(NCOM)Cmhd>/Ostf1<tm1(NCOM)Cmhd>	C57BL/6-Ostf1<tm1(NCOM)Cmhd>	N	28936620
MGI:6107551	M	MP:0000130	abnormal trabecular bone morphology	Ostf1<tm1(NCOM)Cmhd>/Ostf1<tm1(NCOM)Cmhd>	C57BL/6-Ostf1<tm1(NCOM)Cmhd>	N	28936620
MGI:6107640	F	MP:0005266	abnormal metabolism	Mmachc<Gt(AZ0348)Wtsi>/Mmachc<+>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	N	24889031
MGI:6107640	F	MP:0004179	transmission ratio distortion	Mmachc<Gt(AZ0348)Wtsi>/Mmachc<+>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	N	24889031
MGI:6107640	M	MP:0004179	transmission ratio distortion	Mmachc<Gt(AZ0348)Wtsi>/Mmachc<+>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	N	24889031
MGI:6107640	F	MP:0012335	increased circulating homocysteine level	Mmachc<Gt(AZ0348)Wtsi>/Mmachc<+>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	N	24889031
MGI:6107681	F	MP:0001262	decreased body weight	Rr34<tm1.1Lap>/Rr34<tm1.1Lap>	involves: 129S6/SvEvTac * C57BL/6J	N	27703156
MGI:6107696	F	MP:0001406	abnormal gait	Thap1<tm1.1Meeh>/Thap1<+>	involves: 129S/SvEv * C3H * C57BL/6	N	26376866
MGI:6107696	M	MP:0001406	abnormal gait	Thap1<tm1.1Meeh>/Thap1<+>	involves: 129S/SvEv * C3H * C57BL/6	N	26376866
MGI:6107698	F	MP:0001406	abnormal gait	Thap1<tm1.2Meeh>/Thap1<+>	involves: 129S/SvEv * BALB/cJ * C3H * C57BL/6	N	26376866
MGI:6107698	M	MP:0001406	abnormal gait	Thap1<tm1.2Meeh>/Thap1<+>	involves: 129S/SvEv * BALB/cJ * C3H * C57BL/6	N	26376866
MGI:6108356	F	MP:0001923	reduced female fertility	Kpna7<tm1.1Sgao>/Kpna7<tm1.1Sgao>	involves: 129S1/Sv * 129X1/SvJ	N	20699224
MGI:6108356	F	MP:0001935	decreased litter size	Kpna7<tm1.1Sgao>/Kpna7<tm1.1Sgao>	involves: 129S1/Sv * 129X1/SvJ	N	20699224
MGI:6108356	F	MP:0003077	abnormal cell cycle	Kpna7<tm1.1Sgao>/Kpna7<tm1.1Sgao>	involves: 129S1/Sv * 129X1/SvJ	N	20699224
MGI:6108356	F	MP:0020364	abnormal female germ cell physiology	Kpna7<tm1.1Sgao>/Kpna7<tm1.1Sgao>	involves: 129S1/Sv * 129X1/SvJ	N	20699224
MGI:6108357	F	MP:0001935	decreased litter size	Kpna7<tm1.1Sgao>/Kpna7<+>	involves: 129S1/Sv * 129X1/SvJ	N	20699224
MGI:6108357	F	MP:0001923	reduced female fertility	Kpna7<tm1.1Sgao>/Kpna7<+>	involves: 129S1/Sv * 129X1/SvJ	N	20699224
MGI:6110002	M	MP:0005389	reproductive system phenotype	Plcz1<em1Jparr>/Plcz1<em1Jparr>	C57BL/6-Plcz1<em1Jparr>	Y	28694258
MGI:6110002	M	MP:0001922	reduced male fertility	Plcz1<em1Jparr>/Plcz1<em1Jparr>	C57BL/6-Plcz1<em1Jparr>	N	28694258
MGI:6110004	M	MP:0005389	reproductive system phenotype	Plcz1<em2Jparr>/Plcz1<em2Jparr>	C57BL/6-Plcz1<em2Jparr>	Y	28694258
MGI:6110004	M	MP:0001922	reduced male fertility	Plcz1<em2Jparr>/Plcz1<em2Jparr>	C57BL/6-Plcz1<em2Jparr>	N	28694258
MGI:6110148	M	MP:0012292	decreased slow-wave sleep duration	Upf3b<Gt(IST14619B5)Tigm>/Y	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110148	M	MP:0009454	impaired contextual conditioning behavior	Upf3b<Gt(IST14619B5)Tigm>/Y	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110148	M	MP:0009456	impaired cued conditioning behavior	Upf3b<Gt(IST14619B5)Tigm>/Y	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110148	M	MP:0001513	limb grasping	Upf3b<Gt(IST14619B5)Tigm>/Y	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110148	M	MP:0009142	decreased prepulse inhibition	Upf3b<Gt(IST14619B5)Tigm>/Y	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110148	M	MP:0021198	abnormal sleep duration	Upf3b<Gt(IST14619B5)Tigm>/Y	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110148	M	MP:0020508	decreased dendritic spine density	Upf3b<Gt(IST14619B5)Tigm>/Y	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110148	M	MP:0005377	hearing/vestibular/ear phenotype	Upf3b<Gt(IST14619B5)Tigm>/Y	involves: C57BL/6J * C57BL/6N	Y	28948974
MGI:6110148	M	MP:0012286	decreased frequency of paradoxical sleep	Upf3b<Gt(IST14619B5)Tigm>/Y	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110148	M	MP:0001489	decreased startle reflex	Upf3b<Gt(IST14619B5)Tigm>/Y	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110148	M	MP:0001501	abnormal sleep pattern	Upf3b<Gt(IST14619B5)Tigm>/Y	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110148	M	MP:0011827	impaired neuron differentiation	Upf3b<Gt(IST14619B5)Tigm>/Y	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110148	M	MP:0020393	increased neuronal precursor proliferation	Upf3b<Gt(IST14619B5)Tigm>/Y	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110149	F	MP:0009142	decreased prepulse inhibition	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<Gt(IST14619B5)Tigm>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110149	F	MP:0020508	decreased dendritic spine density	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<Gt(IST14619B5)Tigm>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110149	F	MP:0021198	abnormal sleep duration	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<Gt(IST14619B5)Tigm>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110149	F	MP:0005377	hearing/vestibular/ear phenotype	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<Gt(IST14619B5)Tigm>	involves: C57BL/6J * C57BL/6N	Y	28948974
MGI:6110149	F	MP:0001489	decreased startle reflex	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<Gt(IST14619B5)Tigm>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110149	F	MP:0020393	increased neuronal precursor proliferation	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<Gt(IST14619B5)Tigm>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110149	F	MP:0001501	abnormal sleep pattern	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<Gt(IST14619B5)Tigm>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110149	F	MP:0009454	impaired contextual conditioning behavior	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<Gt(IST14619B5)Tigm>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110149	F	MP:0012292	decreased slow-wave sleep duration	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<Gt(IST14619B5)Tigm>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110149	F	MP:0001513	limb grasping	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<Gt(IST14619B5)Tigm>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110149	F	MP:0009456	impaired cued conditioning behavior	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<Gt(IST14619B5)Tigm>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110149	F	MP:0011827	impaired neuron differentiation	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<Gt(IST14619B5)Tigm>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110149	F	MP:0012286	decreased frequency of paradoxical sleep	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<Gt(IST14619B5)Tigm>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110150	F	MP:0009456	impaired cued conditioning behavior	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<+>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110150	F	MP:0009454	impaired contextual conditioning behavior	Upf3b<Gt(IST14619B5)Tigm>/Upf3b<+>	involves: C57BL/6J * C57BL/6N	N	28948974
MGI:6110578	M	MP:0008261	arrest of male meiosis	Tex19.1<tm2.2Ics>/Tex19.1<tm2.2Ics>,Tex19.2<tm1.2Ics>/Tex19.2<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6 * SJL	N	28254886
MGI:6110578	M	MP:0009452	abnormal synaptonemal complex	Tex19.1<tm2.2Ics>/Tex19.1<tm2.2Ics>,Tex19.2<tm1.2Ics>/Tex19.2<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6 * SJL	N	28254886
MGI:6110578	M	MP:0005159	azoospermia	Tex19.1<tm2.2Ics>/Tex19.1<tm2.2Ics>,Tex19.2<tm1.2Ics>/Tex19.2<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6 * SJL	N	28254886
MGI:6110578	F	MP:0002082	postnatal lethality	Tex19.1<tm2.2Ics>/Tex19.1<tm2.2Ics>,Tex19.2<tm1.2Ics>/Tex19.2<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6 * SJL	N	28254886
MGI:6110578	M	MP:0004852	decreased testis weight	Tex19.1<tm2.2Ics>/Tex19.1<tm2.2Ics>,Tex19.2<tm1.2Ics>/Tex19.2<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6 * SJL	N	28254886
MGI:6110578	M	MP:0001925	male infertility	Tex19.1<tm2.2Ics>/Tex19.1<tm2.2Ics>,Tex19.2<tm1.2Ics>/Tex19.2<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6 * SJL	N	28254886
MGI:6110578	M	MP:0001155	arrest of spermatogenesis	Tex19.1<tm2.2Ics>/Tex19.1<tm2.2Ics>,Tex19.2<tm1.2Ics>/Tex19.2<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6 * SJL	N	28254886
MGI:6110578	M	MP:0001154	seminiferous tubule degeneration	Tex19.1<tm2.2Ics>/Tex19.1<tm2.2Ics>,Tex19.2<tm1.2Ics>/Tex19.2<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6 * SJL	N	28254886
MGI:6110578	M	MP:0013600	testis degeneration	Tex19.1<tm2.2Ics>/Tex19.1<tm2.2Ics>,Tex19.2<tm1.2Ics>/Tex19.2<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6 * SJL	N	28254886
MGI:6111174	M	MP:0006036	abnormal mitochondrial physiology	Pabpn1<tm1.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	N	28575395
MGI:6111174	M	MP:0009404	centrally nucleated skeletal muscle fibers	Pabpn1<tm1.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	N	28575395
MGI:6111174	M	MP:0010959	abnormal oxidative phosphorylation	Pabpn1<tm1.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	N	28575395
MGI:6111174	M	MP:0009417	skeletal muscle atrophy	Pabpn1<tm1.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	N	28575395
MGI:6111174	M	MP:0003806	abnormal nucleotide metabolism	Pabpn1<tm1.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	N	28575395
MGI:6111174	M	MP:0009461	skeletal muscle hypertrophy	Pabpn1<tm1.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	N	28575395
MGI:6111174	M	MP:0009401	increased skeletal muscle fiber diameter	Pabpn1<tm1.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	N	28575395
MGI:6111174	M	MP:0009402	decreased skeletal muscle fiber diameter	Pabpn1<tm1.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	N	28575395
MGI:6111179	M	MP:0009461	skeletal muscle hypertrophy	Pabpn1<tm2.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	N	28575395
MGI:6111179	M	MP:0005369	muscle phenotype	Pabpn1<tm2.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	Y	28575395
MGI:6111179	M	MP:0009417	skeletal muscle atrophy	Pabpn1<tm2.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	N	28575395
MGI:6111179	M	MP:0009401	increased skeletal muscle fiber diameter	Pabpn1<tm2.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	N	28575395
MGI:6111179	M	MP:0009402	decreased skeletal muscle fiber diameter	Pabpn1<tm2.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	N	28575395
MGI:6111179	M	MP:0003806	abnormal nucleotide metabolism	Pabpn1<tm2.2Gpvl>/Pabpn1<+>	involves: C57BL/6 * FVB/N	N	28575395
MGI:6111404	M	MP:0005389	reproductive system phenotype	Tcte1<tm1a(KOMP)Wtsi>/Tcte1<tm1a(KOMP)Wtsi>	C57BL/6N-Tcte1<tm1a(KOMP)Wtsi>	Y	28630322
MGI:6111404	M	MP:0002675	asthenozoospermia	Tcte1<tm1a(KOMP)Wtsi>/Tcte1<tm1a(KOMP)Wtsi>	C57BL/6N-Tcte1<tm1a(KOMP)Wtsi>	N	28630322
MGI:6111404	M	MP:0008892	abnormal sperm flagellum morphology	Tcte1<tm1a(KOMP)Wtsi>/Tcte1<tm1a(KOMP)Wtsi>	C57BL/6N-Tcte1<tm1a(KOMP)Wtsi>	N	28630322
MGI:6111404	M	MP:0001925	male infertility	Tcte1<tm1a(KOMP)Wtsi>/Tcte1<tm1a(KOMP)Wtsi>	C57BL/6N-Tcte1<tm1a(KOMP)Wtsi>	N	28630322
MGI:6111404	F	MP:0005389	reproductive system phenotype	Tcte1<tm1a(KOMP)Wtsi>/Tcte1<tm1a(KOMP)Wtsi>	C57BL/6N-Tcte1<tm1a(KOMP)Wtsi>	Y	28630322
MGI:6111404	M	MP:0001124	abnormal gametes	Tcte1<tm1a(KOMP)Wtsi>/Tcte1<tm1a(KOMP)Wtsi>	C57BL/6N-Tcte1<tm1a(KOMP)Wtsi>	N	28630322
MGI:6112643	M	MP:0009141	increased prepulse inhibition	D130043K22Rik<tm1b(KOMP)Wtsi>/D130043K22Rik<tm1b(KOMP)Wtsi>	involves: C57BL/6 * CBA	N	27510895
MGI:6114163	F	MP:0009404	centrally nucleated skeletal muscle fibers	Cav3<tm1Ncnp>/Cav3<+>,Dmd<mdx>/Dmd<mdx>	involves: 129S4/SvJae * C57BL/10 * C57BL/10ScSn	N	19535499
MGI:6114163	F	MP:0000733	abnormal muscle development	Cav3<tm1Ncnp>/Cav3<+>,Dmd<mdx>/Dmd<mdx>	involves: 129S4/SvJae * C57BL/10 * C57BL/10ScSn	N	19535499
MGI:6114163	F	MP:0004087	abnormal muscle fiber morphology	Cav3<tm1Ncnp>/Cav3<+>,Dmd<mdx>/Dmd<mdx>	involves: 129S4/SvJae * C57BL/10 * C57BL/10ScSn	N	19535499
MGI:6114163	F	MP:0002280	abnormal intercostal muscle morphology	Cav3<tm1Ncnp>/Cav3<+>,Dmd<mdx>/Dmd<mdx>	involves: 129S4/SvJae * C57BL/10 * C57BL/10ScSn	N	19535499
MGI:6114768	M	MP:0004851	increased testis weight	Cdkn2a<em1Cjs>/Cdkn2a<em1Cjs>	B6.Cg-Cdkn2a<em1Cjs>	N	28652370
MGI:6114768	M	MP:0005389	reproductive system phenotype	Cdkn2a<em1Cjs>/Cdkn2a<em1Cjs>	B6.Cg-Cdkn2a<em1Cjs>	Y	28652370
MGI:6114772	M	MP:0006379	abnormal spermatocyte morphology	Cdkn2a<em2Cjs>/Cdkn2a<em2Cjs>	C57BL/6-Cdkn2a<em2Cjs>	N	28652370
MGI:6114772	M	MP:0002687	oligozoospermia	Cdkn2a<em2Cjs>/Cdkn2a<em2Cjs>	C57BL/6-Cdkn2a<em2Cjs>	N	28652370
MGI:6114993	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(CAG-cat,-ALOX15)1868Klv/0,Tg(Pbsn-cre)4Prb/0	involves: C57BL/6 * DBA/2	N	16820097
MGI:6114995	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(CAG-cat,-ALOX15)1868Klv/Tg(CAG-cat,-ALOX15)1868Klv,Tg(Pbsn-cre)4Prb/?	involves: C57BL/6 * DBA/2	N	16820097
MGI:6115021	F	MP:0009142	decreased prepulse inhibition	Otud7a<em1Cpsc>/Otud7a<em1Cpsc>	C57BL/6J-Otud7a<em1Cpsc>	N	29395075
MGI:6115249	M	MP:0012029	abnormal electroretinogram waveform feature	Rp2<Gt(EUCJ0183f04)Hmgu>/Y	involves: C57BL/6 * C57BL/6N	N	25422369
MGI:6115249	M	MP:0031606	increased susceptibility to age-related retinal degeneration	Rp2<Gt(EUCJ0183f04)Hmgu>/Y	involves: C57BL/6 * C57BL/6N	N	25422369
MGI:6115249	M	MP:0012143	decreased a-wave amplitude	Rp2<Gt(EUCJ0183f04)Hmgu>/Y	involves: C57BL/6 * C57BL/6N	N	25422369
MGI:6115249	M	MP:0002090	abnormal vision	Rp2<Gt(EUCJ0183f04)Hmgu>/Y	involves: C57BL/6 * C57BL/6N	N	25422369
MGI:6115249	M	MP:0012144	decreased b-wave amplitude	Rp2<Gt(EUCJ0183f04)Hmgu>/Y	involves: C57BL/6 * C57BL/6N	N	25422369
MGI:6115250	F	MP:0031606	increased susceptibility to age-related retinal degeneration	Rp2<Gt(EUCJ0183f04)Hmgu>/Rp2<Gt(EUCJ0183f04)Hmgu>	involves: C57BL/6 * C57BL/6N	N	25422369
MGI:6115250	F	MP:0012144	decreased b-wave amplitude	Rp2<Gt(EUCJ0183f04)Hmgu>/Rp2<Gt(EUCJ0183f04)Hmgu>	involves: C57BL/6 * C57BL/6N	N	25422369
MGI:6115250	F	MP:0005253	abnormal eye physiology	Rp2<Gt(EUCJ0183f04)Hmgu>/Rp2<Gt(EUCJ0183f04)Hmgu>	involves: C57BL/6 * C57BL/6N	N	25422369
MGI:6115250	F	MP:0012029	abnormal electroretinogram waveform feature	Rp2<Gt(EUCJ0183f04)Hmgu>/Rp2<Gt(EUCJ0183f04)Hmgu>	involves: C57BL/6 * C57BL/6N	N	25422369
MGI:6115250	F	MP:0012143	decreased a-wave amplitude	Rp2<Gt(EUCJ0183f04)Hmgu>/Rp2<Gt(EUCJ0183f04)Hmgu>	involves: C57BL/6 * C57BL/6N	N	25422369
MGI:6115250	F	MP:0012031	abnormal b-wave amplitude	Rp2<Gt(EUCJ0183f04)Hmgu>/Rp2<Gt(EUCJ0183f04)Hmgu>	involves: C57BL/6 * C57BL/6N	N	25422369
MGI:6115250	F	MP:0002090	abnormal vision	Rp2<Gt(EUCJ0183f04)Hmgu>/Rp2<Gt(EUCJ0183f04)Hmgu>	involves: C57BL/6 * C57BL/6N	N	25422369
MGI:6115295	F	MP:0001262	decreased body weight	Tg(ACTB-tetR*)19Ywz/0,Tg(tetO-Vegfa)1Ywz/0	involves: 129S1/Sv * 129X1/SvJ	N	22593269
MGI:6115295	F	MP:0011940	decreased food intake	Tg(ACTB-tetR*)19Ywz/0,Tg(tetO-Vegfa)1Ywz/0	involves: 129S1/Sv * 129X1/SvJ	N	22593269
MGI:6115496	F	MP:0002842	increased systemic arterial blood pressure	Inf2<tm1.1(KOMP)Vlcg>/Inf2<tm1.1(KOMP)Vlcg>	involves: C57BL/6NTac	N	29309034
MGI:6115496	F	MP:0002293	long gestation period	Inf2<tm1.1(KOMP)Vlcg>/Inf2<tm1.1(KOMP)Vlcg>	involves: C57BL/6NTac	N	29309034
MGI:6115516	M	MP:0020550	multinucleated giant male germ cells	Sox30<tm1c(KOMP)Wtsi>/Sox30<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	29247201
MGI:6115516	M	MP:0008279	arrest of spermiogenesis	Sox30<tm1c(KOMP)Wtsi>/Sox30<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	29247201
MGI:6115516	M	MP:0005159	azoospermia	Sox30<tm1c(KOMP)Wtsi>/Sox30<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	29247201
MGI:6115516	M	MP:0001925	male infertility	Sox30<tm1c(KOMP)Wtsi>/Sox30<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	29247201
MGI:6115517	M	MP:0001147	small testis	Sox30<tm1a(KOMP)Wtsi>/Sox30<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	29247201
MGI:6115517	M	MP:0008279	arrest of spermiogenesis	Sox30<tm1a(KOMP)Wtsi>/Sox30<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	29247201
MGI:6115517	M	MP:0020550	multinucleated giant male germ cells	Sox30<tm1a(KOMP)Wtsi>/Sox30<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	29247201
MGI:6115517	M	MP:0001156	abnormal spermatogenesis	Sox30<tm1a(KOMP)Wtsi>/Sox30<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	29247201
MGI:6115517	M	MP:0001925	male infertility	Sox30<tm1a(KOMP)Wtsi>/Sox30<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	29247201
MGI:6115517	M	MP:0006380	abnormal spermatid morphology	Sox30<tm1a(KOMP)Wtsi>/Sox30<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	29247201
MGI:6115517	M	MP:0005159	azoospermia	Sox30<tm1a(KOMP)Wtsi>/Sox30<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	29247201
MGI:6115817	F	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis	Rorc<tm1.1Zsun>/Rorc<tm1.1Zsun>	B6(129S4)-Rorc<tm1.1Zsun>	N	28846085
MGI:6116380	M	MP:0001783	decreased white adipose tissue amount	Lrrc8c<tm1Maim>/Lrrc8c<tm1Maim>	B6J.129S2-Lrrc8c<tm1Maim>	N	21804215
MGI:6116380	M	MP:0005659	decreased susceptibility to diet-induced obesity	Lrrc8c<tm1Maim>/Lrrc8c<tm1Maim>	B6J.129S2-Lrrc8c<tm1Maim>	N	21804215
MGI:6116380	M	MP:0002891	increased insulin sensitivity	Lrrc8c<tm1Maim>/Lrrc8c<tm1Maim>	B6J.129S2-Lrrc8c<tm1Maim>	N	21804215
MGI:6116380	M	MP:0003402	decreased liver weight	Lrrc8c<tm1Maim>/Lrrc8c<tm1Maim>	B6J.129S2-Lrrc8c<tm1Maim>	N	21804215
MGI:6116695	M	MP:0005389	reproductive system phenotype	Ccdc62<repro29>/Ccdc62<+>	involves: C3HeB/FeJ * C57BL/6J	Y	28339613
MGI:6116697	M	MP:0002675	asthenozoospermia	Ccdc62<em1Jxia>/Ccdc62<em1Jxia>	C57BL/6-Ccdc62<em1Jxia>	N	28339613
MGI:6116697	M	MP:0009831	abnormal sperm midpiece morphology	Ccdc62<em1Jxia>/Ccdc62<em1Jxia>	C57BL/6-Ccdc62<em1Jxia>	N	28339613
MGI:6116697	M	MP:0001925	male infertility	Ccdc62<em1Jxia>/Ccdc62<em1Jxia>	C57BL/6-Ccdc62<em1Jxia>	N	28339613
MGI:6116697	M	MP:0005578	teratozoospermia	Ccdc62<em1Jxia>/Ccdc62<em1Jxia>	C57BL/6-Ccdc62<em1Jxia>	N	28339613
MGI:6116697	F	MP:0005389	reproductive system phenotype	Ccdc62<em1Jxia>/Ccdc62<em1Jxia>	C57BL/6-Ccdc62<em1Jxia>	Y	28339613
MGI:6116697	M	MP:0009230	abnormal sperm head morphology	Ccdc62<em1Jxia>/Ccdc62<em1Jxia>	C57BL/6-Ccdc62<em1Jxia>	N	28339613
MGI:6116698	M	MP:0005389	reproductive system phenotype	Ccdc62<em1Jxia>/Ccdc62<+>	C57BL/6-Ccdc62<em1Jxia>	Y	28339613
MGI:6117338	F	MP:0003631	nervous system phenotype	Pcdh19<tm1Tac>/Pcdh19<tm1Tac>	involves: 129S/SvEv * C57BL/6	Y	27240640
MGI:6117338	F	MP:0005386	behavior/neurological phenotype	Pcdh19<tm1Tac>/Pcdh19<tm1Tac>	involves: 129S/SvEv * C57BL/6	Y	27240640
MGI:6117338	F	MP:0006009	abnormal neuronal migration	Pcdh19<tm1Tac>/Pcdh19<tm1Tac>	involves: 129S/SvEv * C57BL/6	N	27240640
MGI:6117338	F	MP:0003631	nervous system phenotype	Pcdh19<tm1Tac>/Pcdh19<tm1Tac>	involves: 129S/SvEv * C57BL/6	Y	29301106
MGI:6117339	F	MP:0005386	behavior/neurological phenotype	Pcdh19<tm1Tac>/Pcdh19<+>	involves: 129S/SvEv * C57BL/6	Y	27240640
MGI:6117339	F	MP:0004994	abnormal brain wave pattern	Pcdh19<tm1Tac>/Pcdh19<+>	involves: 129S/SvEv * C57BL/6	N	29301106
MGI:6117339	F	MP:0003631	nervous system phenotype	Pcdh19<tm1Tac>/Pcdh19<+>	involves: 129S/SvEv * C57BL/6	Y	27240640
MGI:6117340	M	MP:0003631	nervous system phenotype	Pcdh19<tm1Tac>/Y	involves: 129S/SvEv * C57BL/6	Y	27240640
MGI:6117340	M	MP:0006009	abnormal neuronal migration	Pcdh19<tm1Tac>/Y	involves: 129S/SvEv * C57BL/6	N	27240640
MGI:6117340	M	MP:0005386	behavior/neurological phenotype	Pcdh19<tm1Tac>/Y	involves: 129S/SvEv * C57BL/6	Y	27240640
MGI:6117341	F	MP:0003232	abnormal forebrain development	Pcdh19<tm1Tac>/Pcdh19<em1Pqt>	involves: 129S/SvEv * C57BL/6	N	29301106
MGI:6117720	M	MP:0004889	increased energy expenditure	Tmem18<tm1a(EUCOMM)Wtsi>/Tmem18<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tmem18<tm1a(EUCOMM)Wtsi>	N	28811369
MGI:6117720	M	MP:0001260	increased body weight	Tmem18<tm1a(EUCOMM)Wtsi>/Tmem18<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tmem18<tm1a(EUCOMM)Wtsi>	N	28811369
MGI:6117720	M	MP:0014142	increased body fat mass	Tmem18<tm1a(EUCOMM)Wtsi>/Tmem18<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tmem18<tm1a(EUCOMM)Wtsi>	N	28811369
MGI:6117720	M	MP:0014170	increased brown adipose tissue mass	Tmem18<tm1a(EUCOMM)Wtsi>/Tmem18<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tmem18<tm1a(EUCOMM)Wtsi>	N	28811369
MGI:6117720	M	MP:0009285	increased gonadal fat pad weight	Tmem18<tm1a(EUCOMM)Wtsi>/Tmem18<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tmem18<tm1a(EUCOMM)Wtsi>	N	28811369
MGI:6117720	M	MP:0005658	increased susceptibility to diet-induced obesity	Tmem18<tm1a(EUCOMM)Wtsi>/Tmem18<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tmem18<tm1a(EUCOMM)Wtsi>	N	28811369
MGI:6117720	M	MP:0003960	increased lean body mass	Tmem18<tm1a(EUCOMM)Wtsi>/Tmem18<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tmem18<tm1a(EUCOMM)Wtsi>	N	28811369
MGI:6117720	M	MP:0011939	increased food intake	Tmem18<tm1a(EUCOMM)Wtsi>/Tmem18<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tmem18<tm1a(EUCOMM)Wtsi>	N	28811369
MGI:6117752	M	MP:0005560	decreased circulating glucose level	C1qtnf7<tm1(KOMP)Vlcg>/C1qtnf7<tm1(KOMP)Vlcg>	C57BL/6N-C1qtnf7<tm1(KOMP)Vlcg>	N	28223291
MGI:6117752	M	MP:0005292	improved glucose tolerance	C1qtnf7<tm1(KOMP)Vlcg>/C1qtnf7<tm1(KOMP)Vlcg>	C57BL/6N-C1qtnf7<tm1(KOMP)Vlcg>	N	28223291
MGI:6117761	M	MP:0006380	abnormal spermatid morphology	Upf3a<tm1.1Wilk>/Upf3a<tm1.1Wilk>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	27040500
MGI:6117761	M	MP:0006378	abnormal spermatogonia morphology	Upf3a<tm1.1Wilk>/Upf3a<tm1.1Wilk>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	27040500
MGI:6117761	M	MP:0005169	abnormal male meiosis	Upf3a<tm1.1Wilk>/Upf3a<tm1.1Wilk>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	27040500
MGI:6117761	M	MP:0002687	oligozoospermia	Upf3a<tm1.1Wilk>/Upf3a<tm1.1Wilk>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	27040500
MGI:6117761	M	MP:0014052	increased male germ cell apoptosis	Upf3a<tm1.1Wilk>/Upf3a<tm1.1Wilk>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	27040500
MGI:6117761	M	MP:0006379	abnormal spermatocyte morphology	Upf3a<tm1.1Wilk>/Upf3a<tm1.1Wilk>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	27040500
MGI:6117761	M	MP:0005384	cellular phenotype	Upf3a<tm1.1Wilk>/Upf3a<tm1.1Wilk>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	Y	27040500
MGI:6117761	M	MP:0005621	abnormal cell physiology	Upf3a<tm1.1Wilk>/Upf3a<tm1.1Wilk>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	27040500
MGI:6117761	M	MP:0004901	decreased male germ cell number	Upf3a<tm1.1Wilk>/Upf3a<tm1.1Wilk>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	27040500
MGI:6117762	M	MP:0006379	abnormal spermatocyte morphology	Tg(Stra8-icre)1Reb/0,Upf3a<tm1.1Wilk>/Upf3a<+>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	27040500
MGI:6117762	M	MP:0004901	decreased male germ cell number	Tg(Stra8-icre)1Reb/0,Upf3a<tm1.1Wilk>/Upf3a<+>	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	27040500
MGI:6117873	M	MP:0004852	decreased testis weight	Morc2b<tm1Jw>/Morc2b<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	29329290
MGI:6117873	M	MP:0005159	azoospermia	Morc2b<tm1Jw>/Morc2b<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	29329290
MGI:6117873	M	MP:0001925	male infertility	Morc2b<tm1Jw>/Morc2b<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	29329290
MGI:6117873	F	MP:0031474	increased female germ cell apoptosis	Morc2b<tm1Jw>/Morc2b<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	29329290
MGI:6117873	M	MP:0001930	abnormal meiosis	Morc2b<tm1Jw>/Morc2b<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	29329290
MGI:6117873	F	MP:0005168	abnormal female meiosis	Morc2b<tm1Jw>/Morc2b<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	29329290
MGI:6117873	M	MP:0014052	increased male germ cell apoptosis	Morc2b<tm1Jw>/Morc2b<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	29329290
MGI:6117873	F	MP:0004805	absent oocytes	Morc2b<tm1Jw>/Morc2b<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	29329290
MGI:6117873	F	MP:0001127	small ovary	Morc2b<tm1Jw>/Morc2b<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	29329290
MGI:6117873	M	MP:0008261	arrest of male meiosis	Morc2b<tm1Jw>/Morc2b<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	29329290
MGI:6117873	M	MP:0001147	small testis	Morc2b<tm1Jw>/Morc2b<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	29329290
MGI:6117873	M	MP:0010948	abnormal double-strand DNA break repair	Morc2b<tm1Jw>/Morc2b<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	29329290
MGI:6117873	F	MP:0001926	female infertility	Morc2b<tm1Jw>/Morc2b<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	29329290
MGI:6118056	M	MP:0005389	reproductive system phenotype	X/Eif2s3y<em1Asah>	involves: C57BL/6 * DBA/2	Y	25579647
MGI:6118057	M	MP:0004852	decreased testis weight	X/Eif2s3y<em2Asah>	involves: C57BL/6 * DBA/2	N	25579647
MGI:6118057	M	MP:0005389	reproductive system phenotype	X/Eif2s3y<em2Asah>	involves: C57BL/6 * DBA/2	Y	25579647
MGI:6118057	M	MP:0005159	azoospermia	X/Eif2s3y<em2Asah>	involves: C57BL/6 * DBA/2	N	25579647
MGI:6118057	M	MP:0001940	testis hypoplasia	X/Eif2s3y<em2Asah>	involves: C57BL/6 * DBA/2	N	25579647
MGI:6118057	M	MP:0006379	abnormal spermatocyte morphology	X/Eif2s3y<em2Asah>	involves: C57BL/6 * DBA/2	N	25579647
MGI:6118057	M	MP:0001925	male infertility	X/Eif2s3y<em2Asah>	involves: C57BL/6 * DBA/2	N	25579647
MGI:6118057	M	MP:0002685	abnormal spermatogonia proliferation	X/Eif2s3y<em2Asah>	involves: C57BL/6 * DBA/2	N	25579647
MGI:6118057	M	MP:0006380	abnormal spermatid morphology	X/Eif2s3y<em2Asah>	involves: C57BL/6 * DBA/2	N	25579647
MGI:6118058	M	MP:0001940	testis hypoplasia	X/Eif2s3y<em#Asah>	involves: C57BL/6 * DBA/2	N	25579647
MGI:6118058	M	MP:0001925	male infertility	X/Eif2s3y<em#Asah>	involves: C57BL/6 * DBA/2	N	25579647
MGI:6118058	M	MP:0005389	reproductive system phenotype	X/Eif2s3y<em#Asah>	involves: C57BL/6 * DBA/2	Y	25579647
MGI:6118058	M	MP:0002685	abnormal spermatogonia proliferation	X/Eif2s3y<em#Asah>	involves: C57BL/6 * DBA/2	N	25579647
MGI:6118058	M	MP:0005159	azoospermia	X/Eif2s3y<em#Asah>	involves: C57BL/6 * DBA/2	N	25579647
MGI:6118058	M	MP:0004852	decreased testis weight	X/Eif2s3y<em#Asah>	involves: C57BL/6 * DBA/2	N	25579647
MGI:6118197	F	MP:0002962	increased urine protein level	Apela<tm1.2Brre>/Apela<tm1.2Brre>	B6(Cg)-Apela<tm1.2Brre>	N	28663440
MGI:6118197	F	MP:0011433	glomerular capillary congestion	Apela<tm1.2Brre>/Apela<tm1.2Brre>	B6(Cg)-Apela<tm1.2Brre>	N	28663440
MGI:6118197	F	MP:0011453	abnormal glomerular capillary endothelium morphology	Apela<tm1.2Brre>/Apela<tm1.2Brre>	B6(Cg)-Apela<tm1.2Brre>	N	28663440
MGI:6118197	F	MP:0011455	absent glomerular endothelium fenestra	Apela<tm1.2Brre>/Apela<tm1.2Brre>	B6(Cg)-Apela<tm1.2Brre>	N	28663440
MGI:6118197	F	MP:0002842	increased systemic arterial blood pressure	Apela<tm1.2Brre>/Apela<tm1.2Brre>	B6(Cg)-Apela<tm1.2Brre>	N	28663440
MGI:6118197	F	MP:0005367	renal/urinary system phenotype	Apela<tm1.2Brre>/Apela<tm1.2Brre>	B6(Cg)-Apela<tm1.2Brre>	Y	28663440
MGI:6118197	F	MP:0001933	abnormal litter size	Apela<tm1.2Brre>/Apela<tm1.2Brre>	B6(Cg)-Apela<tm1.2Brre>	N	28663440
MGI:6118197	F	MP:0003718	maternal effect	Apela<tm1.2Brre>/Apela<tm1.2Brre>	B6(Cg)-Apela<tm1.2Brre>	N	28663440
MGI:6118197	F	MP:0020518	renal glomerular protein deposits	Apela<tm1.2Brre>/Apela<tm1.2Brre>	B6(Cg)-Apela<tm1.2Brre>	N	28663440
MGI:6118198	F	MP:0001933	abnormal litter size	Apela<tm1.2Brre>/Apela<+>	B6(Cg)-Apela<tm1.2Brre>	N	28663440
MGI:6118198	F	MP:0003718	maternal effect	Apela<tm1.2Brre>/Apela<+>	B6(Cg)-Apela<tm1.2Brre>	N	28663440
MGI:6118932	F	MP:0009251	enlarged endometrial glands	Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118932	F	MP:0001923	reduced female fertility	Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118932	F	MP:0005185	decreased circulating progesterone level	Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118932	F	MP:0001935	decreased litter size	Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118932	F	MP:0013401	increased endometrial gland number	Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118932	F	MP:0008995	early reproductive senescence	Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118932	F	MP:0004896	abnormal endometrium morphology	Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118932	F	MP:0009082	uterus cyst	Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118932	F	MP:0009094	abnormal endometrial gland morphology	Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118932	F	MP:0008876	decreased uterine NK cell number	Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118933	F	MP:0009251	enlarged endometrial glands	Pgrmc2<tm1.1Jjp>/Pgrmc2<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118934	F	MP:0009251	enlarged endometrial glands	Pgrmc1<tm1.1Jjp>/Pgrmc1<tm1.1Jjp>,Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118934	F	MP:0009094	abnormal endometrial gland morphology	Pgrmc1<tm1.1Jjp>/Pgrmc1<tm1.1Jjp>,Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118934	F	MP:0004896	abnormal endometrium morphology	Pgrmc1<tm1.1Jjp>/Pgrmc1<tm1.1Jjp>,Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118934	F	MP:0009082	uterus cyst	Pgrmc1<tm1.1Jjp>/Pgrmc1<tm1.1Jjp>,Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118934	F	MP:0013401	increased endometrial gland number	Pgrmc1<tm1.1Jjp>/Pgrmc1<tm1.1Jjp>,Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118934	F	MP:0001923	reduced female fertility	Pgrmc1<tm1.1Jjp>/Pgrmc1<tm1.1Jjp>,Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118934	F	MP:0008995	early reproductive senescence	Pgrmc1<tm1.1Jjp>/Pgrmc1<tm1.1Jjp>,Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118934	F	MP:0001935	decreased litter size	Pgrmc1<tm1.1Jjp>/Pgrmc1<tm1.1Jjp>,Pgrmc2<tm1.1Jjp>/Pgrmc2<tm1.1Jjp>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6118935	F	MP:0009251	enlarged endometrial glands	Pgrmc1<tm1.1Jjp>/Pgrmc1<tm1.1Jjp>,Pgrmc2<tm1.1Jjp>/Pgrmc2<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28005395
MGI:6119468	F	MP:0003944	abnormal T cell subpopulation ratio	H2-D1<b-em5Dvs>/H2-D1<b-em5Dvs>,H2-K1<d-em1Dvs>/H2-K1<d-em1Dvs>	NOD/ShiLtDvs-H2-K1<d-em1Dvs> H2-D1<b-em5Dvs>/Dvs	N	29472249
MGI:6119468	F	MP:0004804	decreased susceptibility to autoimmune diabetes	H2-D1<b-em5Dvs>/H2-D1<b-em5Dvs>,H2-K1<d-em1Dvs>/H2-K1<d-em1Dvs>	NOD/ShiLtDvs-H2-K1<d-em1Dvs> H2-D1<b-em5Dvs>/Dvs	N	29472249
MGI:6119478	F	MP:0001844	autoimmune response	H2-D1<b-em5Dvs>/H2-D1<b-em5Dvs>,H2-K1<d-em1Dvs>/H2-K1<d-em1Dvs>,Tg(HLA-B39/H2-D/B2m)2Dvs/?	NOD/ShiLtDvs-H2-K1<d-em1Dvs> H2-D1<b-em5Dvs> Tg(HLA-B39/H2-D/B2M)2Dvs/Dvs	N	29472249
MGI:6119478	F	MP:0004031	insulitis	H2-D1<b-em5Dvs>/H2-D1<b-em5Dvs>,H2-K1<d-em1Dvs>/H2-K1<d-em1Dvs>,Tg(HLA-B39/H2-D/B2m)2Dvs/?	NOD/ShiLtDvs-H2-K1<d-em1Dvs> H2-D1<b-em5Dvs> Tg(HLA-B39/H2-D/B2M)2Dvs/Dvs	N	29472249
MGI:6119478	F	MP:0004803	increased susceptibility to autoimmune diabetes	H2-D1<b-em5Dvs>/H2-D1<b-em5Dvs>,H2-K1<d-em1Dvs>/H2-K1<d-em1Dvs>,Tg(HLA-B39/H2-D/B2m)2Dvs/?	NOD/ShiLtDvs-H2-K1<d-em1Dvs> H2-D1<b-em5Dvs> Tg(HLA-B39/H2-D/B2M)2Dvs/Dvs	N	29472249
MGI:6119484	F	MP:0001844	autoimmune response	H2-D1<b-em5Dvs>/H2-D1<b-em5Dvs>,H2-K1<d-em1Dvs>/H2-K1<d-em1Dvs>,Tg(HLA-A/H2-D/B2M)1Dvs/?	NOD/ShiLtDvs-H2-K1<d-em1Dvs> H2-D1<b-em5Dvs> Tg(HLA-A/H2-D/B2M)1Dvs/Dvs	N	29472249
MGI:6119570	F	MP:0012765	decreased alpha-beta T cell number	H2-Ab1<g7-em1Dvs>/H2-Ab1<g7-em1Dvs>,H2-D1<b-em5Dvs>/H2-D1<b-em5Dvs>,H2-K1<d-em1Dvs>/H2-K1<d-em1Dvs>	NOD/ShiLtDvs-H2-K1<d-em1Dvs> H2-Ab1<g7-em1Dvs> H2-D1<em5Dvs>/Dvs	N	29472249
MGI:6119570	F	MP:0004804	decreased susceptibility to autoimmune diabetes	H2-Ab1<g7-em1Dvs>/H2-Ab1<g7-em1Dvs>,H2-D1<b-em5Dvs>/H2-D1<b-em5Dvs>,H2-K1<d-em1Dvs>/H2-K1<d-em1Dvs>	NOD/ShiLtDvs-H2-K1<d-em1Dvs> H2-Ab1<g7-em1Dvs> H2-D1<em5Dvs>/Dvs	N	29472249
MGI:6119570	F	MP:0008075	decreased CD4-positive, alpha-beta T cell number	H2-Ab1<g7-em1Dvs>/H2-Ab1<g7-em1Dvs>,H2-D1<b-em5Dvs>/H2-D1<b-em5Dvs>,H2-K1<d-em1Dvs>/H2-K1<d-em1Dvs>	NOD/ShiLtDvs-H2-K1<d-em1Dvs> H2-Ab1<g7-em1Dvs> H2-D1<em5Dvs>/Dvs	N	29472249
MGI:6119570	F	MP:0003944	abnormal T cell subpopulation ratio	H2-Ab1<g7-em1Dvs>/H2-Ab1<g7-em1Dvs>,H2-D1<b-em5Dvs>/H2-D1<b-em5Dvs>,H2-K1<d-em1Dvs>/H2-K1<d-em1Dvs>	NOD/ShiLtDvs-H2-K1<d-em1Dvs> H2-Ab1<g7-em1Dvs> H2-D1<em5Dvs>/Dvs	N	29472249
MGI:6119780	F	MP:0010163	hemolysis	Mfsd2b<tm1a(KOMP)Wtsi>/Mfsd2b<tm1a(KOMP)Wtsi>	C57BL/6-Mfsd2b<tm1a(KOMP)Wtsi>	N	29045386
MGI:6119780	M	MP:0020116	increased sphingosine level	Mfsd2b<tm1a(KOMP)Wtsi>/Mfsd2b<tm1a(KOMP)Wtsi>	C57BL/6-Mfsd2b<tm1a(KOMP)Wtsi>	N	29045386
MGI:6119780	F	MP:0020116	increased sphingosine level	Mfsd2b<tm1a(KOMP)Wtsi>/Mfsd2b<tm1a(KOMP)Wtsi>	C57BL/6-Mfsd2b<tm1a(KOMP)Wtsi>	N	29045386
MGI:6120560	M	MP:0013905	preputial gland inflammation	Gt(ROSA)26Sor<tm1.1(DUX4*)Plj>/Gt(ROSA)26Sor<tm1.1(DUX4*)Plj>	B6(Cg)-Gt(ROSA)26Sor<tm1.1(DUX4*)Plj>	N	29415061
MGI:6121436	M	MP:0013288	premature acrosome reaction	Lcn6<tm1.1Ylzh>/Lcn6<tm1.1Ylzh>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	29045572
MGI:6121436	M	MP:0004543	abnormal sperm physiology	Lcn6<tm1.1Ylzh>/Lcn6<tm1.1Ylzh>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	29045572
MGI:6121436	M	MP:0004231	abnormal calcium ion homeostasis	Lcn6<tm1.1Ylzh>/Lcn6<tm1.1Ylzh>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	29045572
MGI:6121462	M	MP:0001925	male infertility	Mir34a<tm1.1Pisc>/Mir34a<tm1.1Pisc>,Mirc21<tm1.1Pisc>/Mirc21<tm1.1Pisc>,Mirc34<tm1.1Pisc>/Mirc34<tm1.1Pisc>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	N	28923932
MGI:6121462	M	MP:0002687	oligozoospermia	Mir34a<tm1.1Pisc>/Mir34a<tm1.1Pisc>,Mirc21<tm1.1Pisc>/Mirc21<tm1.1Pisc>,Mirc34<tm1.1Pisc>/Mirc34<tm1.1Pisc>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	N	28923932
MGI:6121462	M	MP:0002216	abnormal seminiferous tubule morphology	Mir34a<tm1.1Pisc>/Mir34a<tm1.1Pisc>,Mirc21<tm1.1Pisc>/Mirc21<tm1.1Pisc>,Mirc34<tm1.1Pisc>/Mirc34<tm1.1Pisc>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	N	28923932
MGI:6121462	F	MP:0001926	female infertility	Mir34a<tm1.1Pisc>/Mir34a<tm1.1Pisc>,Mirc21<tm1.1Pisc>/Mirc21<tm1.1Pisc>,Mirc34<tm1.1Pisc>/Mirc34<tm1.1Pisc>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	N	28923932
MGI:6121462	F	MP:0012018	abnormal oviduct physiology	Mir34a<tm1.1Pisc>/Mir34a<tm1.1Pisc>,Mirc21<tm1.1Pisc>/Mirc21<tm1.1Pisc>,Mirc34<tm1.1Pisc>/Mirc34<tm1.1Pisc>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	N	28923932
MGI:6121462	F	MP:0003700	abnormal oviduct transport	Mir34a<tm1.1Pisc>/Mir34a<tm1.1Pisc>,Mirc21<tm1.1Pisc>/Mirc21<tm1.1Pisc>,Mirc34<tm1.1Pisc>/Mirc34<tm1.1Pisc>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	N	28923932
MGI:6147628	M	MP:0003402	decreased liver weight	Saa3<tm1(KOMP)Vlcg>/Saa3<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25251243
MGI:6147628	F	MP:0005179	decreased circulating cholesterol level	Saa3<tm1(KOMP)Vlcg>/Saa3<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25251243
MGI:6147628	F	MP:0000183	decreased circulating LDL cholesterol level	Saa3<tm1(KOMP)Vlcg>/Saa3<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25251243
MGI:6147628	M	MP:0009118	increased white fat cell size	Saa3<tm1(KOMP)Vlcg>/Saa3<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25251243
MGI:6147628	F	MP:0002644	decreased circulating triglyceride level	Saa3<tm1(KOMP)Vlcg>/Saa3<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	25251243
MGI:6147629	F	MP:0000183	decreased circulating LDL cholesterol level	Saa3<tm1(KOMP)Vlcg>/Saa3<+>	involves: C57BL/6NTac	N	25251243
MGI:6149598	M	MP:0020451	decreased sperm progressive motility	Ano5<tm1.2Naga>/Ano5<tm1.2Naga>	involves: C57BL/6	N	26667038
MGI:6149598	M	MP:0005389	reproductive system phenotype	Ano5<tm1.2Naga>/Ano5<tm1.2Naga>	involves: C57BL/6	Y	26667038
MGI:6149598	M	MP:0009280	decreased activated sperm motility	Ano5<tm1.2Naga>/Ano5<tm1.2Naga>	involves: C57BL/6	N	26667038
MGI:6149598	M	MP:0001922	reduced male fertility	Ano5<tm1.2Naga>/Ano5<tm1.2Naga>	involves: C57BL/6	N	26667038
MGI:6149752	M	MP:0030969	increased circulating adiponectin level	Arv1<tm1.2Radr>/Arv1<tm1.2Radr>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ	N	26479315
MGI:6149752	F	MP:0013245	abnormal lipid metabolism	Arv1<tm1.2Radr>/Arv1<tm1.2Radr>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ	N	26479315
MGI:6149752	M	MP:0013278	decreased fasting circulating glucose level	Arv1<tm1.2Radr>/Arv1<tm1.2Radr>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ	N	26479315
MGI:6149752	M	MP:0005292	improved glucose tolerance	Arv1<tm1.2Radr>/Arv1<tm1.2Radr>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ	N	26479315
MGI:6149752	F	MP:0001926	female infertility	Arv1<tm1.2Radr>/Arv1<tm1.2Radr>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ	N	26479315
MGI:6149752	M	MP:0005668	decreased circulating leptin level	Arv1<tm1.2Radr>/Arv1<tm1.2Radr>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ	N	26479315
MGI:6149752	M	MP:0005376	homeostasis/metabolism phenotype	Arv1<tm1.2Radr>/Arv1<tm1.2Radr>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ	Y	26479315
MGI:6149752	F	MP:0014171	increased fatty acid oxidation	Arv1<tm1.2Radr>/Arv1<tm1.2Radr>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ	N	26479315
MGI:6149755	F	MP:0001923	reduced female fertility	Nup107<em1Rajk>/Nup107<em1Rajk>	Not Specified	N	29363275
MGI:6150674	M	MP:0001650	abnormal seizure response to electrical stimulation	Del(7Chrna7-Fan1)3Arte/+	involves: C57BL/6J * C57BL/6NTac	N	24090792
MGI:6150674	M	MP:0000950	abnormal seizure response to pharmacological agent	Del(7Chrna7-Fan1)3Arte/+	involves: C57BL/6J * C57BL/6NTac	N	24090792
MGI:6150674	M	MP:0004738	abnormal auditory brainstem response	Del(7Chrna7-Fan1)3Arte/+	involves: C57BL/6J * C57BL/6NTac	N	24090792
MGI:6150674	M	MP:0005386	behavior/neurological phenotype	Del(7Chrna7-Fan1)3Arte/+	involves: C57BL/6J * C57BL/6NTac	Y	24090792
MGI:6150674	M	MP:0001353	increased aggression towards mice	Del(7Chrna7-Fan1)3Arte/+	involves: C57BL/6J * C57BL/6NTac	N	24090792
MGI:6150674	M	MP:0003631	nervous system phenotype	Del(7Chrna7-Fan1)3Arte/+	involves: C57BL/6J * C57BL/6NTac	Y	24090792
MGI:6150674	M	MP:0001260	increased body weight	Del(7Chrna7-Fan1)3Arte/+	involves: C57BL/6J * C57BL/6NTac	N	24090792
MGI:6150674	M	MP:0002887	decreased susceptibility to pharmacologically induced seizures	Del(7Chrna7-Fan1)3Arte/+	involves: C57BL/6J * C57BL/6NTac	N	24090792
MGI:6150674	M	MP:0001489	decreased startle reflex	Del(7Chrna7-Fan1)3Arte/+	involves: C57BL/6J * C57BL/6NTac	N	24090792
MGI:6150674	M	MP:0001402	decreased locomotor activity	Del(7Chrna7-Fan1)3Arte/+	involves: C57BL/6J * C57BL/6NTac	N	24090792
MGI:6150674	M	MP:0012307	impaired spatial learning	Del(7Chrna7-Fan1)3Arte/+	involves: C57BL/6J * C57BL/6NTac	N	24090792
MGI:6151045	F	MP:0005385	cardiovascular system phenotype	Gpr37l1<tm1d(EUCOMM)Wtsi>/Gpr37l1<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * SJL	Y	29625592
MGI:6151045	F	MP:0006144	increased systemic arterial systolic blood pressure	Gpr37l1<tm1d(EUCOMM)Wtsi>/Gpr37l1<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * SJL	N	29625592
MGI:6151045	F	MP:0004875	increased mean systemic arterial blood pressure	Gpr37l1<tm1d(EUCOMM)Wtsi>/Gpr37l1<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * SJL	N	29625592
MGI:6151045	F	MP:0006265	increased pulse pressure	Gpr37l1<tm1d(EUCOMM)Wtsi>/Gpr37l1<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * SJL	N	29625592
MGI:6151045	F	MP:0006143	increased systemic arterial diastolic blood pressure	Gpr37l1<tm1d(EUCOMM)Wtsi>/Gpr37l1<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * SJL	N	29625592
MGI:6151045	F	MP:0003638	abnormal response/metabolism to endogenous compounds	Gpr37l1<tm1d(EUCOMM)Wtsi>/Gpr37l1<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * SJL	N	29625592
MGI:6151046	F	MP:0006144	increased systemic arterial systolic blood pressure	Gpr37l1<tm1d(EUCOMM)Wtsi>/Gpr37l1<+>	involves: BALB/cJ * C57BL/6N * SJL	N	29625592
MGI:6152755	M	MP:0003666	impaired sperm capacitation	Cabyr<em1Osb>/Cabyr<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27802166
MGI:6152755	M	MP:0020451	decreased sperm progressive motility	Cabyr<em1Osb>/Cabyr<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27802166
MGI:6152755	M	MP:0001922	reduced male fertility	Cabyr<em1Osb>/Cabyr<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27802166
MGI:6152755	M	MP:0009838	abnormal sperm axoneme morphology	Cabyr<em1Osb>/Cabyr<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27802166
MGI:6152755	M	MP:0008892	abnormal sperm flagellum morphology	Cabyr<em1Osb>/Cabyr<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27802166
MGI:6152755	M	MP:0009280	decreased activated sperm motility	Cabyr<em1Osb>/Cabyr<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27802166
MGI:6152755	M	MP:0030590	abnormal sperm fibrous sheath morphology	Cabyr<em1Osb>/Cabyr<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27802166
MGI:6152755	M	MP:0003698	abnormal male reproductive system physiology	Cabyr<em1Osb>/Cabyr<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27802166
MGI:6152755	M	MP:0009836	abnormal sperm principal piece morphology	Cabyr<em1Osb>/Cabyr<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27802166
MGI:6152755	M	MP:0002674	abnormal sperm motility	Cabyr<em1Osb>/Cabyr<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27802166
MGI:6153205	M	MP:0005389	reproductive system phenotype	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	Y	27666520
MGI:6153207	M	MP:0002687	oligozoospermia	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153207	M	MP:0004852	decreased testis weight	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153207	M	MP:0005578	teratozoospermia	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153207	M	MP:0001146	abnormal testis morphology	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153207	M	MP:0001153	small seminiferous tubules	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153207	M	MP:0006362	abnormal male germ cell morphology	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153207	M	MP:0014052	increased male germ cell apoptosis	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153207	M	MP:0001922	reduced male fertility	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153207	M	MP:0001147	small testis	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<+>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153207	M	MP:0005389	reproductive system phenotype	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<+>	involves: 129P2/OlaHsd * C57BL/6J	Y	27666520
MGI:6153208	M	MP:0006362	abnormal male germ cell morphology	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<+>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153208	M	MP:0001925	male infertility	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<+>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153208	M	MP:0001153	small seminiferous tubules	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<+>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153208	M	MP:0001147	small testis	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<+>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153208	M	MP:0002687	oligozoospermia	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<+>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153208	M	MP:0005578	teratozoospermia	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<+>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153208	M	MP:0001146	abnormal testis morphology	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<+>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153208	M	MP:0014052	increased male germ cell apoptosis	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<+>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153208	M	MP:0005389	reproductive system phenotype	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<+>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	Y	27666520
MGI:6153208	M	MP:0004852	decreased testis weight	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<+>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	27666520
MGI:6153209	M	MP:0005378	growth/size/body region phenotype	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<+>,Tg(CAG-Ptp4a2,-EGFP)11Zyz/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	Y	27666520
MGI:6153209	M	MP:0005389	reproductive system phenotype	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<+>,Tg(CAG-Ptp4a2,-EGFP)11Zyz/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	Y	27666520
MGI:6153210	M	MP:0005389	reproductive system phenotype	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<+>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>,Tg(CAG-Ptp4a2,-EGFP)11Zyz/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	Y	27666520
MGI:6153210	M	MP:0005378	growth/size/body region phenotype	Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<+>,Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>,Tg(CAG-Ptp4a2,-EGFP)11Zyz/0	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	Y	27666520
MGI:6153211	M	MP:0005389	reproductive system phenotype	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>,Tg(CAG-Ptp4a2,-EGFP)11Zyz/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	Y	27666520
MGI:6153211	M	MP:0005378	growth/size/body region phenotype	Ptp4a2<Gt(AQ0673)Wtsi>/Ptp4a2<Gt(AQ0673)Wtsi>,Tg(CAG-Ptp4a2,-EGFP)11Zyz/0	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	Y	27666520
MGI:6154041	F	MP:0001926	female infertility	Mtcl1<Gt(AT0556)Wtsi>/Mtcl1<Gt(AT0556)Wtsi>	B6.129P2-Mtcl1<Gt(AT0556)Wtsi>	N	28283581
MGI:6154363	M	MP:0005387	immune system phenotype	Tcra<tm1Mjo>/Tcra<tm1Mjo>,X/Yaa	BXSB.129P2(Cg)-Tcra<tm1Mjo>/Theo	Y	11490025
MGI:6154712	F	MP:0009506	abnormal mammary gland alveolus morphology	Oas2<M1Apb>/Oas2<M1Apb>	involves: C57BL/6J * CBA/CaJ	N	29117179
MGI:6154712	F	MP:0006042	increased apoptosis	Oas2<M1Apb>/Oas2<M1Apb>	involves: C57BL/6J * CBA/CaJ	N	29117179
MGI:6154712	F	MP:0005379	endocrine/exocrine gland phenotype	Oas2<M1Apb>/Oas2<M1Apb>	involves: C57BL/6J * CBA/CaJ	Y	29117179
MGI:6154712	F	MP:0006270	abnormal mammary gland growth during lactation	Oas2<M1Apb>/Oas2<M1Apb>	involves: C57BL/6J * CBA/CaJ	N	29117179
MGI:6154712	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Oas2<M1Apb>/Oas2<M1Apb>	involves: C57BL/6J * CBA/CaJ	N	29117179
MGI:6154712	F	MP:0001881	abnormal mammary gland physiology	Oas2<M1Apb>/Oas2<M1Apb>	involves: C57BL/6J * CBA/CaJ	N	29117179
MGI:6154712	F	MP:0010249	lactation failure	Oas2<M1Apb>/Oas2<M1Apb>	involves: C57BL/6J * CBA/CaJ	N	29117179
MGI:6154713	F	MP:0013716	hypolactation	Oas2<M1Apb>/Oas2<+>	involves: C57BL/6J * CBA/CaJ	N	29117179
MGI:6154993	M	MP:0001262	decreased body weight	Depdc5<tm1c(EUCOMM)Hmgu>/Depdc5<tm1c(EUCOMM)Hmgu>,Tg(Syn1-cre)671Jxm/0	involves: C57BL/6N * CBA	N	29274432
MGI:6154994	M	MP:0001262	decreased body weight	Depdc5<tm1c(EUCOMM)Hmgu>/Depdc5<+>,Tg(Syn1-cre)671Jxm/0	involves: C57BL/6N * CBA	N	29274432
MGI:6155603	M	MP:0005154	increased B cell proliferation	Magt1<Gt(IST13422E1)Tigm>/Y	involves: C57BL/6N	N	29581357
MGI:6155603	M	MP:0004939	abnormal B cell morphology	Magt1<Gt(IST13422E1)Tigm>/Y	involves: C57BL/6N	N	29581357
MGI:6155603	M	MP:0008098	decreased plasma cell number	Magt1<Gt(IST13422E1)Tigm>/Y	involves: C57BL/6N	N	29581357
MGI:6155603	M	MP:0008181	increased marginal zone B cell number	Magt1<Gt(IST13422E1)Tigm>/Y	involves: C57BL/6N	N	29581357
MGI:6155603	M	MP:0005018	decreased T cell number	Magt1<Gt(IST13422E1)Tigm>/Y	involves: C57BL/6N	N	29581357
MGI:6155603	M	MP:0005014	increased B cell number	Magt1<Gt(IST13422E1)Tigm>/Y	involves: C57BL/6N	N	29581357
MGI:6156090	M	MP:0031012	impaired sperm migration in female genital tract	Enkur<tm1Hmf>/Enkur<tm1Hmf>	involves: 129 * C57BL/6J	N	29733335
MGI:6156090	M	MP:0001922	reduced male fertility	Enkur<tm1Hmf>/Enkur<tm1Hmf>	involves: 129 * C57BL/6J	N	29733335
MGI:6156090	M	MP:0020451	decreased sperm progressive motility	Enkur<tm1Hmf>/Enkur<tm1Hmf>	involves: 129 * C57BL/6J	N	29733335
MGI:6156090	M	MP:0009647	decreased fertilization frequency	Enkur<tm1Hmf>/Enkur<tm1Hmf>	involves: 129 * C57BL/6J	N	29733335
MGI:6156090	M	MP:0004543	abnormal sperm physiology	Enkur<tm1Hmf>/Enkur<tm1Hmf>	involves: 129 * C57BL/6J	N	29733335
MGI:6156090	M	MP:0001935	decreased litter size	Enkur<tm1Hmf>/Enkur<tm1Hmf>	involves: 129 * C57BL/6J	N	29733335
MGI:6156090	M	MP:0002674	abnormal sperm motility	Enkur<tm1Hmf>/Enkur<tm1Hmf>	involves: 129 * C57BL/6J	N	29733335
MGI:6156090	M	MP:0005386	behavior/neurological phenotype	Enkur<tm1Hmf>/Enkur<tm1Hmf>	involves: 129 * C57BL/6J	Y	29733335
MGI:6156318	M	MP:0014052	increased male germ cell apoptosis	Dnmt3c<rahu>/Dnmt3c<rahu>	involves: C57BL/6J * FVB/NJ	N	28854222
MGI:6156318	M	MP:0005159	azoospermia	Dnmt3c<rahu>/Dnmt3c<rahu>	involves: C57BL/6J * FVB/NJ	N	28854222
MGI:6156318	M	MP:0008878	abnormal DNA methylation during gametogenesis	Dnmt3c<rahu>/Dnmt3c<rahu>	involves: C57BL/6J * FVB/NJ	N	28854222
MGI:6156318	M	MP:0001147	small testis	Dnmt3c<rahu>/Dnmt3c<rahu>	involves: C57BL/6J * FVB/NJ	N	28854222
MGI:6156318	M	MP:0004852	decreased testis weight	Dnmt3c<rahu>/Dnmt3c<rahu>	involves: C57BL/6J * FVB/NJ	N	28854222
MGI:6156318	F	MP:0005389	reproductive system phenotype	Dnmt3c<rahu>/Dnmt3c<rahu>	involves: C57BL/6J * FVB/NJ	Y	28854222
MGI:6156318	M	MP:0006379	abnormal spermatocyte morphology	Dnmt3c<rahu>/Dnmt3c<rahu>	involves: C57BL/6J * FVB/NJ	N	28854222
MGI:6156318	M	MP:0008261	arrest of male meiosis	Dnmt3c<rahu>/Dnmt3c<rahu>	involves: C57BL/6J * FVB/NJ	N	28854222
MGI:6156318	M	MP:0001925	male infertility	Dnmt3c<rahu>/Dnmt3c<rahu>	involves: C57BL/6J * FVB/NJ	N	28854222
MGI:6156319	M	MP:0004852	decreased testis weight	Dnmt3c<em1Sky>/Dnmt3c<rahu>	involves: C57BL/6J * CBA * FVB/NJ	N	28854222
MGI:6156319	F	MP:0005389	reproductive system phenotype	Dnmt3c<em1Sky>/Dnmt3c<rahu>	involves: C57BL/6J * CBA * FVB/NJ	Y	28854222
MGI:6156320	M	MP:0004852	decreased testis weight	Dnmt3c<em4Sky>/Dnmt3c<rahu>	involves: C57BL/6J * CBA * FVB/NJ	N	28854222
MGI:6156320	M	MP:0005159	azoospermia	Dnmt3c<em4Sky>/Dnmt3c<rahu>	involves: C57BL/6J * CBA * FVB/NJ	N	28854222
MGI:6156321	M	MP:0004852	decreased testis weight	Dnmt3c<em2Sky>/Dnmt3c<em2Sky>	involves: C57BL/6 * CBA	N	28854222
MGI:6156321	F	MP:0005389	reproductive system phenotype	Dnmt3c<em2Sky>/Dnmt3c<em2Sky>	involves: C57BL/6 * CBA	Y	28854222
MGI:6156323	M	MP:0005159	azoospermia	Dnmt3c<em2Sky>/Dnmt3c<em3Sky>	involves: C57BL/6 * CBA	N	28854222
MGI:6156323	M	MP:0004852	decreased testis weight	Dnmt3c<em2Sky>/Dnmt3c<em3Sky>	involves: C57BL/6 * CBA	N	28854222
MGI:6156324	M	MP:0005389	reproductive system phenotype	Dnmt3c<em5Sky>/Dnmt3c<em5Sky>	involves: C57BL/6 * CBA	Y	28854222
MGI:6156325	M	MP:0005389	reproductive system phenotype	Dnmt3c<em5Sky>/Dnmt3c<rahu>	involves: C57BL/6J * CBA * FVB/NJ	Y	28854222
MGI:6156877	M	MP:0001925	male infertility	Tdrd5<tm1c(EUCOMM)Hmgu>/Tdrd5<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29317670
MGI:6156877	M	MP:0003205	testicular atrophy	Tdrd5<tm1c(EUCOMM)Hmgu>/Tdrd5<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29317670
MGI:6156877	M	MP:0001155	arrest of spermatogenesis	Tdrd5<tm1c(EUCOMM)Hmgu>/Tdrd5<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29317670
MGI:6156877	M	MP:0004852	decreased testis weight	Tdrd5<tm1c(EUCOMM)Hmgu>/Tdrd5<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29317670
MGI:6156882	M	MP:0001155	arrest of spermatogenesis	Tdrd5<tm1a(EUCOMM)Hmgu>/Tdrd5<tm1a(EUCOMM)Hmgu>	C57BL/6-Tdrd5<tm1a(EUCOMM)Hmgu>	N	29317670
MGI:6156882	M	MP:0001925	male infertility	Tdrd5<tm1a(EUCOMM)Hmgu>/Tdrd5<tm1a(EUCOMM)Hmgu>	C57BL/6-Tdrd5<tm1a(EUCOMM)Hmgu>	N	29317670
MGI:6157429	F	MP:0013148	mastitis	Lao1<tm1Oka>/Lao1<tm1Oka>	involves: 129S2/SvPas * C57BL/6J	N	19276171
MGI:6157429	F	MP:0004047	abnormal milk composition	Lao1<tm1Oka>/Lao1<tm1Oka>	involves: 129S2/SvPas * C57BL/6J	N	19276171
MGI:6157429	F	MP:0005379	endocrine/exocrine gland phenotype	Lao1<tm1Oka>/Lao1<tm1Oka>	involves: 129S2/SvPas * C57BL/6J	Y	19276171
MGI:6157429	F	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality	Lao1<tm1Oka>/Lao1<tm1Oka>	involves: 129S2/SvPas * C57BL/6J	N	19276171
MGI:6157429	F	MP:0002412	increased susceptibility to bacterial infection	Lao1<tm1Oka>/Lao1<tm1Oka>	involves: 129S2/SvPas * C57BL/6J	N	19276171
MGI:6157429	F	MP:0008751	abnormal interleukin level	Lao1<tm1Oka>/Lao1<tm1Oka>	involves: 129S2/SvPas * C57BL/6J	N	19276171
MGI:6157533	M	MP:0008261	arrest of male meiosis	Map7<mshi>/Map7<mshi>	involves: BALB/cBy	N	8875885
MGI:6157533	M	MP:0001925	male infertility	Map7<mshi>/Map7<mshi>	involves: BALB/cBy	N	8875885
MGI:6157533	M	MP:0002216	abnormal seminiferous tubule morphology	Map7<mshi>/Map7<mshi>	involves: BALB/cBy	N	8875885
MGI:6157533	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Map7<mshi>/Map7<mshi>	involves: BALB/cBy	N	8875885
MGI:6157533	M	MP:0006428	ectopic Sertoli cells	Map7<mshi>/Map7<mshi>	involves: BALB/cBy	N	8875885
MGI:6157533	M	MP:0001152	increased Leydig cell number	Map7<mshi>/Map7<mshi>	involves: BALB/cBy	N	8875885
MGI:6157629	M	MP:0003109	short femur	Notch2<tm2.2Ecan>/Notch2<+>	involves: 129S1/Sv * C57BL/6J	N	28592489
MGI:6157651	F	MP:0010933	decreased trabecular bone connectivity density	Notch2<tm2.1Ecan>/Notch2<tm2.1Ecan>,Tg(BGLAP-cre)1Clem/0	involves: C57BL/6J * FVB/NJ	N	28592489
MGI:6157651	F	MP:0010968	decreased compact bone area	Notch2<tm2.1Ecan>/Notch2<tm2.1Ecan>,Tg(BGLAP-cre)1Clem/0	involves: C57BL/6J * FVB/NJ	N	28592489
MGI:6157651	F	MP:0010867	abnormal bone trabecula morphology	Notch2<tm2.1Ecan>/Notch2<tm2.1Ecan>,Tg(BGLAP-cre)1Clem/0	involves: C57BL/6J * FVB/NJ	N	28592489
MGI:6157651	F	MP:0010879	decreased trabecular bone volume	Notch2<tm2.1Ecan>/Notch2<tm2.1Ecan>,Tg(BGLAP-cre)1Clem/0	involves: C57BL/6J * FVB/NJ	N	28592489
MGI:6157651	F	MP:0009346	decreased trabecular bone thickness	Notch2<tm2.1Ecan>/Notch2<tm2.1Ecan>,Tg(BGLAP-cre)1Clem/0	involves: C57BL/6J * FVB/NJ	N	28592489
MGI:6157651	F	MP:0010869	decreased bone trabecula number	Notch2<tm2.1Ecan>/Notch2<tm2.1Ecan>,Tg(BGLAP-cre)1Clem/0	involves: C57BL/6J * FVB/NJ	N	28592489
MGI:6157651	F	MP:0013630	increased bone trabecular spacing	Notch2<tm2.1Ecan>/Notch2<tm2.1Ecan>,Tg(BGLAP-cre)1Clem/0	involves: C57BL/6J * FVB/NJ	N	28592489
MGI:6157819	F	MP:0001923	reduced female fertility	Tinagl1<tm1.1Maru>/Tinagl1<tm1.1Maru>	involves: 129S2/SvPas * C57BL/6NSlc	N	26522507
MGI:6157853	M	MP:0001925	male infertility	Cfap43<em1Pfr>/Cfap43<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157853	M	MP:0031438	abnormal sperm radial spoke morphology	Cfap43<em1Pfr>/Cfap43<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157853	M	MP:0009241	thick sperm flagellum	Cfap43<em1Pfr>/Cfap43<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157853	M	MP:0009238	coiled sperm flagellum	Cfap43<em1Pfr>/Cfap43<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157853	M	MP:0005578	teratozoospermia	Cfap43<em1Pfr>/Cfap43<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157853	M	MP:0008892	abnormal sperm flagellum morphology	Cfap43<em1Pfr>/Cfap43<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157853	M	MP:0031352	absent sperm axonemal central pair	Cfap43<em1Pfr>/Cfap43<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157853	M	MP:0009239	short sperm flagellum	Cfap43<em1Pfr>/Cfap43<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157853	M	MP:0020869	immotile sperm	Cfap43<em1Pfr>/Cfap43<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157853	M	MP:0009838	abnormal sperm axoneme morphology	Cfap43<em1Pfr>/Cfap43<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157853	M	MP:0009230	abnormal sperm head morphology	Cfap43<em1Pfr>/Cfap43<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157854	M	MP:0020451	decreased sperm progressive motility	Cfap43<em1Pfr>/Cfap43<+>	involves: C57BL/6J	N	29449551
MGI:6157855	M	MP:0002675	asthenozoospermia	Cfap44<em1Pfr>/Cfap44<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157855	M	MP:0001925	male infertility	Cfap44<em1Pfr>/Cfap44<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157855	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Cfap44<em1Pfr>/Cfap44<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157855	M	MP:0009838	abnormal sperm axoneme morphology	Cfap44<em1Pfr>/Cfap44<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157855	M	MP:0005578	teratozoospermia	Cfap44<em1Pfr>/Cfap44<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157855	M	MP:0031356	abnormal outer dense fiber morphology	Cfap44<em1Pfr>/Cfap44<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157855	M	MP:0030590	abnormal sperm fibrous sheath morphology	Cfap44<em1Pfr>/Cfap44<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157855	M	MP:0009836	abnormal sperm principal piece morphology	Cfap44<em1Pfr>/Cfap44<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157855	M	MP:0009831	abnormal sperm midpiece morphology	Cfap44<em1Pfr>/Cfap44<em1Pfr>	involves: C57BL/6J	N	29449551
MGI:6157856	M	MP:0005578	teratozoospermia	Cfap44<em1Pfr>/Cfap44<+>	involves: C57BL/6J	N	29449551
MGI:6159136	M	MP:0013630	increased bone trabecular spacing	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Runx2-icre)1Jtuc/0	involves: FVB/N	N	29621230
MGI:6159136	M	MP:0020137	decreased bone mineralization	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Runx2-icre)1Jtuc/0	involves: FVB/N	N	29621230
MGI:6159136	M	MP:0020039	increased bone ossification	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Runx2-icre)1Jtuc/0	involves: FVB/N	N	29621230
MGI:6159136	M	MP:0013638	decreased femur stiffness	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Runx2-icre)1Jtuc/0	involves: FVB/N	N	29621230
MGI:6159136	M	MP:0000061	fragile skeleton	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Runx2-icre)1Jtuc/0	involves: FVB/N	N	29621230
MGI:6159136	F	MP:0008156	decreased diameter of tibia	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Runx2-icre)1Jtuc/0	involves: FVB/N	N	29621230
MGI:6159136	M	MP:0005006	abnormal osteoblast physiology	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Runx2-icre)1Jtuc/0	involves: FVB/N	N	29621230
MGI:6159136	M	MP:0010933	decreased trabecular bone connectivity density	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Runx2-icre)1Jtuc/0	involves: FVB/N	N	29621230
MGI:6159136	M	MP:0003797	abnormal compact bone morphology	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Runx2-icre)1Jtuc/0	involves: FVB/N	N	29621230
MGI:6159158	M	MP:0005382	craniofacial phenotype	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Ctsk-cre)1Rda/0	involves: C57BL/6	Y	29621230
MGI:6159158	F	MP:0013631	decreased bone trabecular spacing	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Ctsk-cre)1Rda/0	involves: C57BL/6	N	29621230
MGI:6159158	M	MP:0020080	increased bone mineralization	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Ctsk-cre)1Rda/0	involves: C57BL/6	N	29621230
MGI:6159158	M	MP:0000558	abnormal tibia morphology	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Ctsk-cre)1Rda/0	involves: C57BL/6	N	29621230
MGI:6159158	M	MP:0020040	decreased bone ossification	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Ctsk-cre)1Rda/0	involves: C57BL/6	N	29621230
MGI:6159158	F	MP:0010878	increased trabecular bone volume	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Ctsk-cre)1Rda/0	involves: C57BL/6	N	29621230
MGI:6159158	F	MP:0010868	increased bone trabecula number	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Ctsk-cre)1Rda/0	involves: C57BL/6	N	29621230
MGI:6159158	F	MP:0009347	increased trabecular bone thickness	Gt(ROSA)26Sor<tm1(CAG-Slc39a14*L438R)Wvh>/Gt(ROSA)26Sor<+>,Tg(Ctsk-cre)1Rda/0	involves: C57BL/6	N	29621230
MGI:6159252	M	MP:0002781	increased circulating testosterone level	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0004851	increased testis weight	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0001152	increased Leydig cell number	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0001148	enlarged testis	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0001260	increased body weight	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0004909	increased seminal vesicle weight	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0002997	enlarged seminal vesicle	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0030603	increased sperm number	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0005646	abnormal pituitary gland physiology	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0004884	abnormal testis physiology	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0002216	abnormal seminiferous tubule morphology	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0013604	abnormal adult Leydig cell differentiation	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0002059	abnormal seminal vesicle morphology	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0001751	increased circulating luteinizing hormone level	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	M	MP:0002669	abnormal scrotum morphology	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159252	F	MP:0001923	reduced female fertility	Prl3c1<tm1(KOMP)Vlcg>/Prl3c1<tm1(KOMP)Vlcg>	involves: C57BL/6NTac * CD-1	N	28576872
MGI:6159280	M	MP:0000063	decreased bone mineral density	Fam210a<tm1c(EUCOMM)Wtsi>/Fam210a<tm1c(EUCOMM)Wtsi>,Tg(ACTA1-cre/Esr1*)2Kesr/0	involves: C3H * C57BL/6N * SJL	N	29618611
MGI:6159334	F	MP:0001392	abnormal locomotor behavior	Mecp2<em1Dkatz>/Mecp2<+>,Tyr<c-ch>/Tyr<c-ch>	FVB.Cg-Pde6b<+> Tyr<c-ch> Mecp2<em1Dkatz>/J	N	MGI:3606206
MGI:6159334	F	MP:0005389	reproductive system phenotype	Mecp2<em1Dkatz>/Mecp2<+>,Tyr<c-ch>/Tyr<c-ch>	FVB.Cg-Pde6b<+> Tyr<c-ch> Mecp2<em1Dkatz>/J	Y	MGI:3606206
MGI:6159335	F	MP:0001926	female infertility	Mecp2<em1Dkatz>/Mecp2<em1Dkatz>,Tyr<c-ch>/Tyr<c-ch>	FVB.Cg-Pde6b<+> Tyr<c-ch> Mecp2<em1Dkatz>/J	N	MGI:3606206
MGI:6159336	M	MP:0002083	premature death	Mecp2<em1Dkatz>/Y,Tyr<c-ch>/Tyr<c-ch>	FVB.Cg-Pde6b<+> Tyr<c-ch> Mecp2<em1Dkatz>/J	N	MGI:3606206
MGI:6159374	M	MP:0001147	small testis	Tg(Ddx4-cre)1Dcas/0,Uxt<tm1.1Sklo>/Y	involves: 129S1/Sv * C57BL/6 * FVB	N	29649254
MGI:6159374	M	MP:0001156	abnormal spermatogenesis	Tg(Ddx4-cre)1Dcas/0,Uxt<tm1.1Sklo>/Y	involves: 129S1/Sv * C57BL/6 * FVB	N	29649254
MGI:6159374	M	MP:0008261	arrest of male meiosis	Tg(Ddx4-cre)1Dcas/0,Uxt<tm1.1Sklo>/Y	involves: 129S1/Sv * C57BL/6 * FVB	N	29649254
MGI:6159374	M	MP:0005159	azoospermia	Tg(Ddx4-cre)1Dcas/0,Uxt<tm1.1Sklo>/Y	involves: 129S1/Sv * C57BL/6 * FVB	N	29649254
MGI:6159374	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Tg(Ddx4-cre)1Dcas/0,Uxt<tm1.1Sklo>/Y	involves: 129S1/Sv * C57BL/6 * FVB	N	29649254
MGI:6159374	M	MP:0004852	decreased testis weight	Tg(Ddx4-cre)1Dcas/0,Uxt<tm1.1Sklo>/Y	involves: 129S1/Sv * C57BL/6 * FVB	N	29649254
MGI:6159374	M	MP:0014052	increased male germ cell apoptosis	Tg(Ddx4-cre)1Dcas/0,Uxt<tm1.1Sklo>/Y	involves: 129S1/Sv * C57BL/6 * FVB	N	29649254
MGI:6159375	M	MP:0011091	prenatal lethality, complete penetrance	Uxt<tm1.2Sklo>/Y	involves: 129S1/Sv * C57BL/6	N	29649254
MGI:6159376	F	MP:0011091	prenatal lethality, complete penetrance	Uxt<tm1.2Sklo>/Uxt<+>	involves: 129S1/Sv * C57BL/6	N	29649254
MGI:6159704	M	MP:0009355	increased liver triglyceride level	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0030880	abnormal infrapatellar fat pad morphology	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0011174	lipodystrophy	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0014169	decreased brown adipose tissue mass	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0000187	abnormal triglyceride level	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0002970	abnormal white adipose tissue morphology	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0005376	homeostasis/metabolism phenotype	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	Y	29459250
MGI:6159704	M	MP:0001402	decreased locomotor activity	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0005659	decreased susceptibility to diet-induced obesity	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0010378	increased respiratory quotient	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0001783	decreased white adipose tissue amount	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0031008	decreased bone marrow adipose tissue amount	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0010379	decreased respiratory quotient	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0030968	decreased circulating adiponectin level	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0014143	decreased body fat mass	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0008844	decreased subcutaneous adipose tissue amount	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0002971	abnormal brown adipose tissue morphology	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0003960	increased lean body mass	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159704	M	MP:0020521	browned white adipose tissue morphology	Bscl2<tm1c(EUCOMM)Hmgu>/Bscl2<tm1c(EUCOMM)Hmgu>,Tg(Adipoq-cre)1Evdr/0	involves: C57BL/6N * FVB/NJ	N	29459250
MGI:6159882	F	MP:0005389	reproductive system phenotype	Igsf8<tm1.2Osb>/Igsf8<tm1.2Osb>	involves: 129S2/SvPas * C57BL/6J	Y	22609062
MGI:6159936	M	MP:0001147	small testis	Pnldc1<em1Nkn>/Pnldc1<em1Nkn>	involves: C57BL/6	N	29444933
MGI:6159936	M	MP:0008877	abnormal DNA methylation	Pnldc1<em1Nkn>/Pnldc1<em1Nkn>	involves: C57BL/6	N	29444933
MGI:6159936	M	MP:0001155	arrest of spermatogenesis	Pnldc1<em1Nkn>/Pnldc1<em1Nkn>	involves: C57BL/6	N	29444933
MGI:6159936	M	MP:0001925	male infertility	Pnldc1<em1Nkn>/Pnldc1<em1Nkn>	involves: C57BL/6	N	29444933
MGI:6159937	M	MP:0008877	abnormal DNA methylation	Pnldc1<em2Nkn>/Pnldc1<em2Nkn>	involves: C57BL/6	N	29444933
MGI:6159937	M	MP:0001147	small testis	Pnldc1<em2Nkn>/Pnldc1<em2Nkn>	involves: C57BL/6	N	29444933
MGI:6159937	M	MP:0001155	arrest of spermatogenesis	Pnldc1<em2Nkn>/Pnldc1<em2Nkn>	involves: C57BL/6	N	29444933
MGI:6159937	M	MP:0001925	male infertility	Pnldc1<em2Nkn>/Pnldc1<em2Nkn>	involves: C57BL/6	N	29444933
MGI:6160399	M	MP:0002169	no abnormal phenotype detected	Ftx<tm1.1Oka>/Y	B6(Cg)-Ftx<tm1.1Oka>	N	24899465
MGI:6160401	F	MP:0002169	no abnormal phenotype detected	Ftx<tm1.1Oka>/Ftx<+>	(C57BL/6N x B6(Cg)-Ftx<tm1.1Oka>)F1	N	24899465
MGI:6160754	M	MP:0003631	nervous system phenotype	Plp1<tm1c(EUCOMM)Wtsi>/Y,Neurod6<tm1(cre)Kan>/Neurod6<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	Y	28836307
MGI:6160757	M	MP:0008918	microgliosis	Plp1<tm1c(EUCOMM)Wtsi>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	28836307
MGI:6160757	M	MP:0003005	abnormal hippocampal fimbria morphology	Plp1<tm1c(EUCOMM)Wtsi>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	28836307
MGI:6160757	M	MP:0003354	astrocytosis	Plp1<tm1c(EUCOMM)Wtsi>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	28836307
MGI:6160757	M	MP:0010047	axonal spheroids	Plp1<tm1c(EUCOMM)Wtsi>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	28836307
MGI:6160757	M	MP:0005015	increased T cell number	Plp1<tm1c(EUCOMM)Wtsi>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	28836307
MGI:6160760	M	MP:0010047	axonal spheroids	Plp1<tm1Kan>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129S1/Sv * 129X1/SvJ	N	28836307
MGI:6160760	M	MP:0003005	abnormal hippocampal fimbria morphology	Plp1<tm1Kan>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129S1/Sv * 129X1/SvJ	N	28836307
MGI:6160760	M	MP:0008918	microgliosis	Plp1<tm1Kan>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129S1/Sv * 129X1/SvJ	N	28836307
MGI:6160760	M	MP:0005015	increased T cell number	Plp1<tm1Kan>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129S1/Sv * 129X1/SvJ	N	28836307
MGI:6160760	M	MP:0003354	astrocytosis	Plp1<tm1Kan>/Y,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129S1/Sv * 129X1/SvJ	N	28836307
MGI:6160805	F	MP:0005654	porphyria	Cpox<Rbc16>/Cpox<+>	involves: C57BL/6	N	28600349
MGI:6160821	M	MP:0002079	increased circulating insulin level	Tg(Ins2-rtTA)2Efr/0,Tg(tetO-Sri)1Hhv/0	involves: C57BL/6 * CBA	N	26822088
MGI:6160821	M	MP:0005292	improved glucose tolerance	Tg(Ins2-rtTA)2Efr/0,Tg(tetO-Sri)1Hhv/0	involves: C57BL/6 * CBA	N	26822088
MGI:6160821	M	MP:0005378	growth/size/body region phenotype	Tg(Ins2-rtTA)2Efr/0,Tg(tetO-Sri)1Hhv/0	involves: C57BL/6 * CBA	Y	26822088
MGI:6160821	M	MP:0002693	abnormal pancreas physiology	Tg(Ins2-rtTA)2Efr/0,Tg(tetO-Sri)1Hhv/0	involves: C57BL/6 * CBA	N	26822088
MGI:6160822	M	MP:0005292	improved glucose tolerance	Tg(Ins2-rtTA)2Efr/0,Tg(tetO-Sri)10Hhv/0	involves: C57BL/6 * CBA	N	26822088
MGI:6160822	M	MP:0002079	increased circulating insulin level	Tg(Ins2-rtTA)2Efr/0,Tg(tetO-Sri)10Hhv/0	involves: C57BL/6 * CBA	N	26822088
MGI:6160822	M	MP:0013278	decreased fasting circulating glucose level	Tg(Ins2-rtTA)2Efr/0,Tg(tetO-Sri)10Hhv/0	involves: C57BL/6 * CBA	N	26822088
MGI:6160822	M	MP:0002693	abnormal pancreas physiology	Tg(Ins2-rtTA)2Efr/0,Tg(tetO-Sri)10Hhv/0	involves: C57BL/6 * CBA	N	26822088
MGI:6160822	M	MP:0005215	abnormal pancreatic islet morphology	Tg(Ins2-rtTA)2Efr/0,Tg(tetO-Sri)10Hhv/0	involves: C57BL/6 * CBA	N	26822088
MGI:6160822	M	MP:0005378	growth/size/body region phenotype	Tg(Ins2-rtTA)2Efr/0,Tg(tetO-Sri)10Hhv/0	involves: C57BL/6 * CBA	Y	26822088
MGI:6160896	M	MP:0008997	increased blood osmolality	Umod<tm1.1Rvt>/Umod<+>	either: B6J.129-Umod<tm1.1Rvt> or (involves: 129S1/Sv * 129X1/SvJ)	N	28325753
MGI:6160896	M	MP:0005553	increased circulating creatinine level	Umod<tm1.1Rvt>/Umod<+>	either: B6J.129-Umod<tm1.1Rvt> or (involves: 129S1/Sv * 129X1/SvJ)	N	28325753
MGI:6160896	M	MP:0001762	polyuria	Umod<tm1.1Rvt>/Umod<+>	either: B6J.129-Umod<tm1.1Rvt> or (involves: 129S1/Sv * 129X1/SvJ)	N	28325753
MGI:6160905	M	MP:0001147	small testis	Shoc1<tm2Rjpz>/Shoc1<tm2Rjpz>	involves: C57BL/6N	N	29742103
MGI:6160905	M	MP:0014052	increased male germ cell apoptosis	Shoc1<tm2Rjpz>/Shoc1<tm2Rjpz>	involves: C57BL/6N	N	29742103
MGI:6160905	M	MP:0001153	small seminiferous tubules	Shoc1<tm2Rjpz>/Shoc1<tm2Rjpz>	involves: C57BL/6N	N	29742103
MGI:6160905	M	MP:0008261	arrest of male meiosis	Shoc1<tm2Rjpz>/Shoc1<tm2Rjpz>	involves: C57BL/6N	N	29742103
MGI:6160905	F	MP:0005389	reproductive system phenotype	Shoc1<tm2Rjpz>/Shoc1<tm2Rjpz>	involves: C57BL/6N	Y	29742103
MGI:6160905	M	MP:0005159	azoospermia	Shoc1<tm2Rjpz>/Shoc1<tm2Rjpz>	involves: C57BL/6N	N	29742103
MGI:6160905	M	MP:0008966	abnormal chiasmata formation	Shoc1<tm2Rjpz>/Shoc1<tm2Rjpz>	involves: C57BL/6N	N	29742103
MGI:6160905	M	MP:0009451	abnormal chromosomal synapsis	Shoc1<tm2Rjpz>/Shoc1<tm2Rjpz>	involves: C57BL/6N	N	29742103
MGI:6160905	M	MP:0004852	decreased testis weight	Shoc1<tm2Rjpz>/Shoc1<tm2Rjpz>	involves: C57BL/6N	N	29742103
MGI:6161342	M	MP:0030586	impaired behavioral response to amphetamine	Scn4b<tm1.2Geh>/Scn4b<tm1.2Geh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	28243192
MGI:6161824	M	MP:0006379	abnormal spermatocyte morphology	Cntd1<tm1e.1(KOMP)Wtsi>/Cntd1<tm1e.1(KOMP)Wtsi>	involves: C57BL/6N	N	24891606
MGI:6161824	M	MP:0001147	small testis	Cntd1<tm1e.1(KOMP)Wtsi>/Cntd1<tm1e.1(KOMP)Wtsi>	involves: C57BL/6N	N	24891606
MGI:6161824	M	MP:0005169	abnormal male meiosis	Cntd1<tm1e.1(KOMP)Wtsi>/Cntd1<tm1e.1(KOMP)Wtsi>	involves: C57BL/6N	N	24891606
MGI:6161824	M	MP:0006380	abnormal spermatid morphology	Cntd1<tm1e.1(KOMP)Wtsi>/Cntd1<tm1e.1(KOMP)Wtsi>	involves: C57BL/6N	N	24891606
MGI:6161824	M	MP:0005159	azoospermia	Cntd1<tm1e.1(KOMP)Wtsi>/Cntd1<tm1e.1(KOMP)Wtsi>	involves: C57BL/6N	N	24891606
MGI:6161824	F	MP:0001926	female infertility	Cntd1<tm1e.1(KOMP)Wtsi>/Cntd1<tm1e.1(KOMP)Wtsi>	involves: C57BL/6N	N	24891606
MGI:6161824	M	MP:0001925	male infertility	Cntd1<tm1e.1(KOMP)Wtsi>/Cntd1<tm1e.1(KOMP)Wtsi>	involves: C57BL/6N	N	24891606
MGI:6161824	F	MP:0005168	abnormal female meiosis	Cntd1<tm1e.1(KOMP)Wtsi>/Cntd1<tm1e.1(KOMP)Wtsi>	involves: C57BL/6N	N	24891606
MGI:6162247	M	MP:0004852	decreased testis weight	Spata16<em2Osb>/Spata16<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	29065458
MGI:6162247	M	MP:0001156	abnormal spermatogenesis	Spata16<em2Osb>/Spata16<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	29065458
MGI:6162247	M	MP:0008892	abnormal sperm flagellum morphology	Spata16<em2Osb>/Spata16<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	29065458
MGI:6162247	M	MP:0009230	abnormal sperm head morphology	Spata16<em2Osb>/Spata16<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	29065458
MGI:6162247	M	MP:0008279	arrest of spermiogenesis	Spata16<em2Osb>/Spata16<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	29065458
MGI:6162247	M	MP:0005578	teratozoospermia	Spata16<em2Osb>/Spata16<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	29065458
MGI:6162247	M	MP:0001925	male infertility	Spata16<em2Osb>/Spata16<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	29065458
MGI:6162247	M	MP:0001147	small testis	Spata16<em2Osb>/Spata16<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	29065458
MGI:6162247	M	MP:0001932	abnormal spermiogenesis	Spata16<em2Osb>/Spata16<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	29065458
MGI:6162247	M	MP:0002687	oligozoospermia	Spata16<em2Osb>/Spata16<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	29065458
MGI:6162248	M	MP:0001925	male infertility	Ccdc136<em1Smoc>/Ccdc136<em1Smoc>	involves: C57BL/6J	N	27076447
MGI:6162248	M	MP:0002675	asthenozoospermia	Ccdc136<em1Smoc>/Ccdc136<em1Smoc>	involves: C57BL/6J	N	27076447
MGI:6162248	M	MP:0009232	abnormal sperm nucleus morphology	Ccdc136<em1Smoc>/Ccdc136<em1Smoc>	involves: C57BL/6J	N	27076447
MGI:6162248	M	MP:0002686	globozoospermia	Ccdc136<em1Smoc>/Ccdc136<em1Smoc>	involves: C57BL/6J	N	27076447
MGI:6162248	M	MP:0009647	decreased fertilization frequency	Ccdc136<em1Smoc>/Ccdc136<em1Smoc>	involves: C57BL/6J	N	27076447
MGI:6162248	M	MP:0020451	decreased sperm progressive motility	Ccdc136<em1Smoc>/Ccdc136<em1Smoc>	involves: C57BL/6J	N	27076447
MGI:6162486	M	MP:0001922	reduced male fertility	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	M	MP:0009203	external male genitalia hypoplasia	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	M	MP:0005578	teratozoospermia	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	F	MP:0001927	abnormal estrous cycle	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	M	MP:0005188	small penis	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	F	MP:0001120	abnormal uterus morphology	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	M	MP:0001147	small testis	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	M	MP:0003550	short perineum	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	M	MP:0005536	decreased Leydig cell number	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	F	MP:0001129	impaired ovarian folliculogenesis	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	M	MP:0001925	male infertility	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	F	MP:0002637	small uterus	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	M	MP:0008940	delayed balanopreputial separation	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	F	MP:0001134	absent corpus luteum	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	F	MP:0002016	ovary cyst	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	F	MP:0011130	absent tertiary ovarian follicles	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	F	MP:0001127	small ovary	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	M	MP:0001154	seminiferous tubule degeneration	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162486	F	MP:0031239	increased atretic ovarian follicle number	Wdr11<Gt(Ayu21-KBW205)Imeg>/Wdr11<Gt(Ayu21-KBW205)Imeg>	B6.Cg-Wdr11<Gt(Ayu21-KBW205)Imeg>	N	29263200
MGI:6162678	M	MP:0001262	decreased body weight	Atp1a3<tm1Ute>/Atp1a3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25523819
MGI:6163481	M	MP:0001147	small testis	Greb1l<em1Cjea>/Greb1l<em1Cjea>	involves: C57BL/6J	N	29100091
MGI:6163481	M	MP:0003830	abnormal testis development	Greb1l<em1Cjea>/Greb1l<em1Cjea>	involves: C57BL/6J	N	29100091
MGI:6163637	M	MP:0009403	increased variability of skeletal muscle fiber size	Dmd<em1Eno>/Y	involves: C57BL/6J	N	29187645
MGI:6163637	M	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<em1Eno>/Y	involves: C57BL/6J	N	29187645
MGI:6163637	M	MP:0004510	myositis	Dmd<em1Eno>/Y	involves: C57BL/6J	N	29187645
MGI:6163637	M	MP:0020280	increased creatine kinase level	Dmd<em1Eno>/Y	involves: C57BL/6J	N	29187645
MGI:6163637	M	MP:0000752	dystrophic muscle	Dmd<em1Eno>/Y	involves: C57BL/6J	N	29187645
MGI:6163637	M	MP:0010053	decreased grip strength	Dmd<em1Eno>/Y	involves: C57BL/6J	N	29187645
MGI:6163637	M	MP:0003852	skeletal muscle necrosis	Dmd<em1Eno>/Y	involves: C57BL/6J	N	29187645
MGI:6163706	M	MP:0031373	abnormal manchette perinuclear ring morphology	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163706	M	MP:0002687	oligozoospermia	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163706	M	MP:0002675	asthenozoospermia	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163706	M	MP:0005578	teratozoospermia	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163706	M	MP:0009230	abnormal sperm head morphology	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163706	M	MP:0001147	small testis	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163706	M	MP:0004852	decreased testis weight	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163706	M	MP:0001925	male infertility	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163706	M	MP:0008892	abnormal sperm flagellum morphology	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163706	M	MP:0006380	abnormal spermatid morphology	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163706	M	MP:0020451	decreased sperm progressive motility	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163706	M	MP:0004901	decreased male germ cell number	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163706	M	MP:0009376	abnormal manchette morphology	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163706	M	MP:0001932	abnormal spermiogenesis	Spata20<Tn(pb-Act-RFP)1.1Zhu>/Spata20<Tn(pb-Act-RFP)1.1Zhu>	FVB/NJ-Spata20<Tn(pb-Act-RFP)1.1Zhu>	N	29247744
MGI:6163736	M	MP:0020337	abnormal pyramidal neuron dendrite morphology	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163736	M	MP:0001265	decreased body size	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163736	M	MP:0001353	increased aggression towards mice	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163736	M	MP:0009456	impaired cued conditioning behavior	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163736	M	MP:0005389	reproductive system phenotype	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	Y	26804915
MGI:6163736	M	MP:0009454	impaired contextual conditioning behavior	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163736	M	MP:0001262	decreased body weight	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163736	M	MP:0001360	abnormal social investigation	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163736	M	MP:0010698	abnormal impulsive behavior control	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163736	M	MP:0001364	decreased anxiety-related response	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163736	M	MP:0009936	abnormal dendritic spine morphology	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163736	M	MP:0020512	abnormal dendritic mushroom spine morphology	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163736	M	MP:0020508	decreased dendritic spine density	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163736	M	MP:0012307	impaired spatial learning	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163736	M	MP:0002781	increased circulating testosterone level	Kdm5c<tm1.2Yshi>/Y	involves: 129 * 129S1/SvImJ * C57BL/6J	N	26804915
MGI:6163819	M	MP:0031356	abnormal outer dense fiber morphology	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6163819	M	MP:0006380	abnormal spermatid morphology	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6163819	M	MP:0008898	abnormal acrosome morphology	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6163819	M	MP:0002687	oligozoospermia	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6163819	M	MP:0009230	abnormal sperm head morphology	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6163819	M	MP:0008839	absent acrosome	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6163819	M	MP:0008892	abnormal sperm flagellum morphology	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6163819	M	MP:0001925	male infertility	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6163819	M	MP:0002675	asthenozoospermia	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6163819	M	MP:0004901	decreased male germ cell number	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6163819	M	MP:0009838	abnormal sperm axoneme morphology	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6163819	M	MP:0004852	decreased testis weight	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6163819	M	MP:0004182	abnormal spermiation	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6163819	M	MP:0031389	abnormal ectoplasmic specialization morphology	Mkrn2<tm1.1Bhj>/Mkrn2<tm1.1Bhj>	involves: 129P2/OlaHsd * C57BL/6J	N	28008940
MGI:6164125	M	MP:0001363	increased anxiety-related response	Tafa3<em1Hssh>/Tafa3<em1Hssh>	C57BL/6NTac-Tafa3<em1Hssh>	N	29184127
MGI:6164125	M	MP:0001409	increased stereotypic behavior	Tafa3<em1Hssh>/Tafa3<em1Hssh>	C57BL/6NTac-Tafa3<em1Hssh>	N	29184127
MGI:6164125	M	MP:0002557	abnormal social/conspecific interaction behavior	Tafa3<em1Hssh>/Tafa3<em1Hssh>	C57BL/6NTac-Tafa3<em1Hssh>	N	29184127
MGI:6164126	M	MP:0001441	increased grooming behavior	Tafa3<em1Hssh>/Tafa3<+>	C57BL/6NTac-Tafa3<em1Hssh>	N	29184127
MGI:6164126	M	MP:0001363	increased anxiety-related response	Tafa3<em1Hssh>/Tafa3<+>	C57BL/6NTac-Tafa3<em1Hssh>	N	29184127
MGI:6164126	M	MP:0001409	increased stereotypic behavior	Tafa3<em1Hssh>/Tafa3<+>	C57BL/6NTac-Tafa3<em1Hssh>	N	29184127
MGI:6164126	F	MP:0031391	increased locomotor activity	Tafa3<em1Hssh>/Tafa3<+>	C57BL/6NTac-Tafa3<em1Hssh>	N	29184127
MGI:6164158	F	MP:0001926	female infertility	Braf<tm1Tumg>/Braf<+>,Tg(CAG-cre)2Osb/0	involves: BALB/c * C57BL * C57BL/6J * DBA	N	26472072
MGI:6164161	F	MP:0001926	female infertility	Braf<tm1Tumg>/Braf<+>,Tg(CAG-cre)2Osb/0	involves: C57BL * C57BL/6J * DBA * ICR	N	26472072
MGI:6164161	F	MP:0002016	ovary cyst	Braf<tm1Tumg>/Braf<+>,Tg(CAG-cre)2Osb/0	involves: C57BL * C57BL/6J * DBA * ICR	N	26472072
MGI:6164170	M	MP:0001147	small testis	Nabp1<tm1.1Kkha>/Nabp1<tm1.1Kkha>	B6.Cg-Nabp1<tm1.1Kkha>	N	25917330
MGI:6164170	M	MP:0004852	decreased testis weight	Nabp1<tm1.1Kkha>/Nabp1<tm1.1Kkha>	B6.Cg-Nabp1<tm1.1Kkha>	N	25917330
MGI:6187681	F	MP:0001130	abnormal ovarian folliculogenesis	Gas2<tm1(GFP/cre/ERT2)Pzg>/Gas2<tm1(GFP/cre/ERT2)Pzg>	involves: 129S7/SvEvBrd * C57BL/6	N	27734842
MGI:6187681	F	MP:0011129	decreased tertiary ovarian follicle number	Gas2<tm1(GFP/cre/ERT2)Pzg>/Gas2<tm1(GFP/cre/ERT2)Pzg>	involves: 129S7/SvEvBrd * C57BL/6	N	27734842
MGI:6187681	F	MP:0008868	abnormal granulosa cell morphology	Gas2<tm1(GFP/cre/ERT2)Pzg>/Gas2<tm1(GFP/cre/ERT2)Pzg>	involves: 129S7/SvEvBrd * C57BL/6	N	27734842
MGI:6187681	F	MP:0001923	reduced female fertility	Gas2<tm1(GFP/cre/ERT2)Pzg>/Gas2<tm1(GFP/cre/ERT2)Pzg>	involves: 129S7/SvEvBrd * C57BL/6	N	27734842
MGI:6187681	F	MP:0002680	decreased corpora lutea number	Gas2<tm1(GFP/cre/ERT2)Pzg>/Gas2<tm1(GFP/cre/ERT2)Pzg>	involves: 129S7/SvEvBrd * C57BL/6	N	27734842
MGI:6187681	F	MP:0003355	decreased ovulation rate	Gas2<tm1(GFP/cre/ERT2)Pzg>/Gas2<tm1(GFP/cre/ERT2)Pzg>	involves: 129S7/SvEvBrd * C57BL/6	N	27734842
MGI:6187681	F	MP:0001935	decreased litter size	Gas2<tm1(GFP/cre/ERT2)Pzg>/Gas2<tm1(GFP/cre/ERT2)Pzg>	involves: 129S7/SvEvBrd * C57BL/6	N	27734842
MGI:6187681	F	MP:0004273	abnormal basal lamina morphology	Gas2<tm1(GFP/cre/ERT2)Pzg>/Gas2<tm1(GFP/cre/ERT2)Pzg>	involves: 129S7/SvEvBrd * C57BL/6	N	27734842
MGI:6187681	F	MP:0003582	abnormal ovary development	Gas2<tm1(GFP/cre/ERT2)Pzg>/Gas2<tm1(GFP/cre/ERT2)Pzg>	involves: 129S7/SvEvBrd * C57BL/6	N	27734842
MGI:6187681	F	MP:0009433	polyovular ovarian follicle	Gas2<tm1(GFP/cre/ERT2)Pzg>/Gas2<tm1(GFP/cre/ERT2)Pzg>	involves: 129S7/SvEvBrd * C57BL/6	N	27734842
MGI:6187681	F	MP:0001126	abnormal ovary morphology	Gas2<tm1(GFP/cre/ERT2)Pzg>/Gas2<tm1(GFP/cre/ERT2)Pzg>	involves: 129S7/SvEvBrd * C57BL/6	N	27734842
MGI:6187717	M	MP:0011110	preweaning lethality, incomplete penetrance	Tardbp<em1Rhbr>/Tardbp<em1Rhbr>	C57BL/6J-Tardbp<em1Rhbr>	N	29556029
MGI:6187717	M	MP:0003245	abnormal GABAergic neuron morphology	Tardbp<em1Rhbr>/Tardbp<em1Rhbr>	C57BL/6J-Tardbp<em1Rhbr>	N	29556029
MGI:6187717	M	MP:0003631	nervous system phenotype	Tardbp<em1Rhbr>/Tardbp<em1Rhbr>	C57BL/6J-Tardbp<em1Rhbr>	Y	29556029
MGI:6187717	M	MP:0001458	abnormal object recognition memory	Tardbp<em1Rhbr>/Tardbp<em1Rhbr>	C57BL/6J-Tardbp<em1Rhbr>	N	29556029
MGI:6187717	M	MP:0004101	abnormal brain interneuron morphology	Tardbp<em1Rhbr>/Tardbp<em1Rhbr>	C57BL/6J-Tardbp<em1Rhbr>	N	29556029
MGI:6187717	M	MP:0001433	polyphagia	Tardbp<em1Rhbr>/Tardbp<em1Rhbr>	C57BL/6J-Tardbp<em1Rhbr>	N	29556029
MGI:6187717	M	MP:0014115	cognitive inflexibility	Tardbp<em1Rhbr>/Tardbp<em1Rhbr>	C57BL/6J-Tardbp<em1Rhbr>	N	29556029
MGI:6187717	M	MP:0014114	abnormal cognition	Tardbp<em1Rhbr>/Tardbp<em1Rhbr>	C57BL/6J-Tardbp<em1Rhbr>	N	29556029
MGI:6187717	M	MP:0001260	increased body weight	Tardbp<em1Rhbr>/Tardbp<em1Rhbr>	C57BL/6J-Tardbp<em1Rhbr>	N	29556029
MGI:6187717	M	MP:0003908	decreased stereotypic behavior	Tardbp<em1Rhbr>/Tardbp<em1Rhbr>	C57BL/6J-Tardbp<em1Rhbr>	N	29556029
MGI:6187718	M	MP:0003908	decreased stereotypic behavior	Tardbp<em1Rhbr>/Tardbp<+>	C57BL/6J-Tardbp<em1Rhbr>	N	29556029
MGI:6187718	M	MP:0001458	abnormal object recognition memory	Tardbp<em1Rhbr>/Tardbp<+>	C57BL/6J-Tardbp<em1Rhbr>	N	29556029
MGI:6187718	M	MP:0001405	impaired coordination	Tardbp<em1Rhbr>/Tardbp<+>	C57BL/6J-Tardbp<em1Rhbr>	N	29556029
MGI:6187718	M	MP:0002063	abnormal learning/memory/conditioning	Tardbp<em1Rhbr>/Tardbp<+>	C57BL/6J-Tardbp<em1Rhbr>	N	29556029
MGI:6187936	F	MP:0001661	extended life span	Ndufa1<tm1.1Nay>/Ndufa1<tm1.1Nay>	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0005266	abnormal metabolism	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0010026	decreased liver cholesterol level	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0005635	decreased circulating bilirubin level	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0002665	decreased circulating corticosterone level	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0004151	decreased circulating iron level	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0000876	Purkinje cell degeneration	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0013242	abnormal amino acid metabolism	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0010379	decreased respiratory quotient	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0005281	increased fatty acids level	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0001402	decreased locomotor activity	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0004890	decreased energy expenditure	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0002078	abnormal glucose homeostasis	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0003806	abnormal nucleotide metabolism	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0002083	premature death	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0013245	abnormal lipid metabolism	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0005278	abnormal cholesterol homeostasis	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0012230	abnormal sphingolipid level	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0003963	abnormal corticosterone level	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0030636	decreased taurine level	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0011940	decreased food intake	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0020234	decreased basal metabolism	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0005311	abnormal circulating amino acid level	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6187937	M	MP:0005290	decreased oxygen consumption	Ndufa1<tm1.1Nay>/Y	involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	N	28506826
MGI:6188064	F	MP:0001923	reduced female fertility	Ddc<tm1Umon>/Ddc<tm1Umon>	involves: 129S/SvEv * C57BL/6 * FVB/N	N	28973165
MGI:6188064	F	MP:0001386	abnormal maternal nurturing	Ddc<tm1Umon>/Ddc<tm1Umon>	involves: 129S/SvEv * C57BL/6 * FVB/N	N	28973165
MGI:6188302	M	MP:0005389	reproductive system phenotype	Spmip9<em1Qsh>/Spmip9<em1Qsh>	involves: C57BL/6 * DBA/2J	Y	29563520
MGI:6188303	M	MP:0005389	reproductive system phenotype	Ccdc73<em1Qsh>/Ccdc73<em1Qsh>	involves: C57BL/6 * DBA/2J	Y	29563520
MGI:6188304	M	MP:0005389	reproductive system phenotype	Prss55<em1Qsh>/Prss55<em1Qsh>	involves: C57BL/6 * DBA/2J	Y	29563520
MGI:6188305	M	MP:0005389	reproductive system phenotype	Lyzl1<em1Qsh>/Lyzl1<em1Qsh>	involves: C57BL/6 * DBA/2J	Y	29563520
MGI:6188306	M	MP:0005389	reproductive system phenotype	Nxt2<em1Qsh>/Nxt2<em1Qsh>	involves: C57BL/6 * DBA/2J	Y	29563520
MGI:6188326	F	MP:0004804	decreased susceptibility to autoimmune diabetes	Lag3<tm1Daav>/Lag3<+>,Tg(Foxp3-EGFP/cre)1cJbs/0	NOD.Cg-Lag3<tm1Daav> Tg(Foxp3-EGFP/cre)1cJbs	N	28783703
MGI:6188974	M	MP:0003084	abnormal skeletal muscle fiber morphology	Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	N	29437892
MGI:6188974	M	MP:0005386	behavior/neurological phenotype	Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	Y	29437892
MGI:6188974	M	MP:0005384	cellular phenotype	Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	Y	29437892
MGI:6188974	M	MP:0005387	immune system phenotype	Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	Y	29437892
MGI:6188975	M	MP:0001732	postnatal growth retardation	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>,Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	N	29437892
MGI:6188975	M	MP:0009402	decreased skeletal muscle fiber diameter	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>,Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	N	29437892
MGI:6188975	M	MP:0002183	gliosis	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>,Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	N	29437892
MGI:6188975	M	MP:0002651	abnormal sciatic nerve morphology	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>,Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	N	29437892
MGI:6188975	M	MP:0001265	decreased body size	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>,Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	N	29437892
MGI:6188975	M	MP:0001255	decreased body height	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>,Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	N	29437892
MGI:6188975	M	MP:0000938	motor neuron degeneration	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>,Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	N	29437892
MGI:6188975	M	MP:0000939	decreased motor neuron number	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>,Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	N	29437892
MGI:6188975	M	MP:0000753	paralysis	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>,Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	N	29437892
MGI:6188975	M	MP:0000920	abnormal myelination	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>,Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	N	29437892
MGI:6188975	M	MP:0010053	decreased grip strength	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>,Scyl3<tm1.1Spel>/Scyl3<tm1.1Spel>	involves: 129S6/SvEvTac * C57BL/6J	N	29437892
MGI:6188976	M	MP:0010053	decreased grip strength	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>	involves: 129S6/SvEvTac	N	29437892
MGI:6188976	M	MP:0001732	postnatal growth retardation	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>	involves: 129S6/SvEvTac	N	29437892
MGI:6188976	M	MP:0000938	motor neuron degeneration	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>	involves: 129S6/SvEvTac	N	29437892
MGI:6188976	M	MP:0002651	abnormal sciatic nerve morphology	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>	involves: 129S6/SvEvTac	N	29437892
MGI:6188976	M	MP:0000920	abnormal myelination	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>	involves: 129S6/SvEvTac	N	29437892
MGI:6188976	M	MP:0002183	gliosis	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>	involves: 129S6/SvEvTac	N	29437892
MGI:6188976	M	MP:0000939	decreased motor neuron number	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>	involves: 129S6/SvEvTac	N	29437892
MGI:6188976	M	MP:0009417	skeletal muscle atrophy	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>	involves: 129S6/SvEvTac	N	29437892
MGI:6188976	M	MP:0009402	decreased skeletal muscle fiber diameter	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>	involves: 129S6/SvEvTac	N	29437892
MGI:6188976	M	MP:0000753	paralysis	Scyl1<tm1.1Spel>/Scyl1<tm1.1Spel>	involves: 129S6/SvEvTac	N	29437892
MGI:6189549	M	MP:0002687	oligozoospermia	Reep6<em2Ruch>/Reep6<em2Ruch>	involves: C57BL/6 * C57BL/6J	N	32101290
MGI:6189549	M	MP:0001925	male infertility	Reep6<em2Ruch>/Reep6<em2Ruch>	involves: C57BL/6 * C57BL/6J	N	32101290
MGI:6189549	M	MP:0004542	impaired acrosome reaction	Reep6<em2Ruch>/Reep6<em2Ruch>	involves: C57BL/6 * C57BL/6J	N	32101290
MGI:6189549	M	MP:0005578	teratozoospermia	Reep6<em2Ruch>/Reep6<em2Ruch>	involves: C57BL/6 * C57BL/6J	N	32101290
MGI:6189549	M	MP:0002675	asthenozoospermia	Reep6<em2Ruch>/Reep6<em2Ruch>	involves: C57BL/6 * C57BL/6J	N	32101290
MGI:6191667	M	MP:0009838	abnormal sperm axoneme morphology	Tssk4<tm1.1Lgyu>/Tssk4<tm1.1Lgyu>	B6.129(129S2)-Tssk4<tm1.1Lgyu>	N	25361759
MGI:6191667	M	MP:0009836	abnormal sperm principal piece morphology	Tssk4<tm1.1Lgyu>/Tssk4<tm1.1Lgyu>	B6.129(129S2)-Tssk4<tm1.1Lgyu>	N	25361759
MGI:6191667	M	MP:0001922	reduced male fertility	Tssk4<tm1.1Lgyu>/Tssk4<tm1.1Lgyu>	B6.129(129S2)-Tssk4<tm1.1Lgyu>	N	25361759
MGI:6191667	M	MP:0009280	decreased activated sperm motility	Tssk4<tm1.1Lgyu>/Tssk4<tm1.1Lgyu>	B6.129(129S2)-Tssk4<tm1.1Lgyu>	N	25361759
MGI:6191667	M	MP:0009831	abnormal sperm midpiece morphology	Tssk4<tm1.1Lgyu>/Tssk4<tm1.1Lgyu>	B6.129(129S2)-Tssk4<tm1.1Lgyu>	N	25361759
MGI:6191667	M	MP:0001935	decreased litter size	Tssk4<tm1.1Lgyu>/Tssk4<tm1.1Lgyu>	B6.129(129S2)-Tssk4<tm1.1Lgyu>	N	25361759
MGI:6191719	M	MP:0031373	abnormal manchette perinuclear ring morphology	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0008898	abnormal acrosome morphology	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0006380	abnormal spermatid morphology	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0005578	teratozoospermia	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0004029	spontaneous chromosome breakage	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0009838	abnormal sperm axoneme morphology	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0008545	absent sperm flagellum	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0001156	abnormal spermatogenesis	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0009230	abnormal sperm head morphology	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0004182	abnormal spermiation	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0002687	oligozoospermia	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0001925	male infertility	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0002675	asthenozoospermia	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0009376	abnormal manchette morphology	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0004852	decreased testis weight	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0004901	decreased male germ cell number	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0009231	detached acrosome	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6191719	M	MP:0009239	short sperm flagellum	Lrguk<Kaos>/Lrguk<Kaos>	involves: C57BL/6 * CBA	N	25781171
MGI:6192446	M	MP:0005378	growth/size/body region phenotype	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	Y	27297240
MGI:6192446	M	MP:0001405	impaired coordination	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	N	27297240
MGI:6192446	M	MP:0010053	decreased grip strength	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	N	27297240
MGI:6192446	M	MP:0000160	kyphosis	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	N	27297240
MGI:6192446	M	MP:0009412	skeletal muscle fiber degeneration	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	N	27297240
MGI:6192446	M	MP:0005386	behavior/neurological phenotype	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	Y	27297240
MGI:6192446	M	MP:0012307	impaired spatial learning	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	N	27297240
MGI:6192446	M	MP:0000754	paresis	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	N	27297240
MGI:6192446	M	MP:0003084	abnormal skeletal muscle fiber morphology	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	N	27297240
MGI:6192446	M	MP:0002083	premature death	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	N	27297240
MGI:6192446	M	MP:0000807	abnormal hippocampus morphology	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	N	27297240
MGI:6192446	M	MP:0001513	limb grasping	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	N	27297240
MGI:6192446	M	MP:0012006	abnormal hippocampus physiology	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	N	27297240
MGI:6192446	M	MP:0008260	abnormal autophagy	Hprt1<tm1(MAPT)Dph>/Y	involves: 129P2/OlaHsd * C57BL/6	N	27297240
MGI:6193618	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Gt(ROSA)26Sor<tm1(CAG-AR)Zsu>/Gt(ROSA)26Sor<tm1(CAG-AR)Zsu>,Tg(Osr1-cre)4Mrt/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	N	21795710
MGI:6193618	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Gt(ROSA)26Sor<tm1(CAG-AR)Zsu>/Gt(ROSA)26Sor<tm1(CAG-AR)Zsu>,Tg(Osr1-cre)4Mrt/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	N	21795710
MGI:6193619	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Gt(ROSA)26Sor<tm1(CAG-AR)Zsu>/Gt(ROSA)26Sor<+>,Tg(Osr1-cre)4Mrt/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	N	21795710
MGI:6193619	M	MP:0002018	increased malignant tumor incidence	Gt(ROSA)26Sor<tm1(CAG-AR)Zsu>/Gt(ROSA)26Sor<+>,Tg(Osr1-cre)4Mrt/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	N	21795710
MGI:6193619	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Gt(ROSA)26Sor<tm1(CAG-AR)Zsu>/Gt(ROSA)26Sor<+>,Tg(Osr1-cre)4Mrt/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	N	21795710
MGI:6193898	M	MP:0003141	cardiac fibrosis	Tg(Myh6-MYL2*D94A)1Dsc/0	Not Specified	N	29463717
MGI:6193925	M	MP:0001547	abnormal lipid level	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0001262	decreased body weight	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0008839	absent acrosome	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0012216	decreased plasmalogen level	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0012230	abnormal sphingolipid level	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0008545	absent sperm flagellum	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0001154	seminiferous tubule degeneration	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0006380	abnormal spermatid morphology	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0001156	abnormal spermatogenesis	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0001922	reduced male fertility	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0001925	male infertility	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0012232	abnormal ceramide level	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0004901	decreased male germ cell number	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0020355	abnormal Sertoli cell barrier morphology	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0013601	increased testis apoptosis	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0005285	decreased unsaturated fatty acids level	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0003402	decreased liver weight	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0009823	abnormal sphingomyelin level	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0020356	abnormal Sertoli cell barrier function	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6193925	M	MP:0001935	decreased litter size	Sgms1<Gt(E201D11)Wrst>/Sgms1<Gt(E201D11)Wrst>	B6.129P2-Sgms1<Gt(E201D11)Wrst>	N	27788151
MGI:6194786	M	MP:0005281	increased fatty acids level	Abcd1<tm1Kan>/Y,Gt(ROSA)26Sor<tm2.1(CAG-ELOVL1)Geno>/Gt(ROSA)26Sor<+>,Cnp<tm1(cre)Kan>/Cnp<+>	involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6J	N	27124591
MGI:6194788	F	MP:0001129	impaired ovarian folliculogenesis	Ythdc1<tm1.1Jw>/Ythdc1<tm1.2Jw>,Tg(Zp3-cre)93Knw/0	involves: 129S4/SvJae * C57BL/6J * FVB	N	29799838
MGI:6194788	F	MP:0001926	female infertility	Ythdc1<tm1.1Jw>/Ythdc1<tm1.2Jw>,Tg(Zp3-cre)93Knw/0	involves: 129S4/SvJae * C57BL/6J * FVB	N	29799838
MGI:6194789	M	MP:0006378	abnormal spermatogonia morphology	Ythdc1<tm1.1Jw>/Ythdc1<tm1.2Jw>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	29799838
MGI:6194789	F	MP:0004805	absent oocytes	Ythdc1<tm1.1Jw>/Ythdc1<tm1.2Jw>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	29799838
MGI:6194789	F	MP:0020845	abnormal DNA-templated transcription	Ythdc1<tm1.1Jw>/Ythdc1<tm1.2Jw>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	29799838
MGI:6194789	M	MP:0005159	azoospermia	Ythdc1<tm1.1Jw>/Ythdc1<tm1.2Jw>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	29799838
MGI:6194789	F	MP:0001129	impaired ovarian folliculogenesis	Ythdc1<tm1.1Jw>/Ythdc1<tm1.2Jw>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	29799838
MGI:6194789	F	MP:0001125	abnormal oocyte morphology	Ythdc1<tm1.1Jw>/Ythdc1<tm1.2Jw>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	29799838
MGI:6194789	F	MP:0011130	absent tertiary ovarian follicles	Ythdc1<tm1.1Jw>/Ythdc1<tm1.2Jw>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	29799838
MGI:6194789	F	MP:0031382	absent secondary ovarian follicles	Ythdc1<tm1.1Jw>/Ythdc1<tm1.2Jw>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB	N	29799838
MGI:6194958	M	MP:0002169	no abnormal phenotype detected	Ubqlnl<em1Osb>/Ubqlnl<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194959	M	MP:0002169	no abnormal phenotype detected	Ubqln3<em1Osb>/Ubqln3<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194960	M	MP:0002169	no abnormal phenotype detected	Ube2u<em1Osb>/Ube2u<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194961	M	MP:0002169	no abnormal phenotype detected	Tmem247<em1Osb>/Tmem247<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194962	M	MP:0002169	no abnormal phenotype detected	Tmco5<em1Osb>/Tmco5<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194963	M	MP:0002169	no abnormal phenotype detected	Tktl1<em1Osb>/Tktl1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194964	M	MP:0002169	no abnormal phenotype detected	Spink8<em2Osb>/Spink8<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194965	M	MP:0002169	no abnormal phenotype detected	Spink8<em1Osb>/Spink8<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194966	M	MP:0002169	no abnormal phenotype detected	Spaca7<em1Osb>/Spaca7<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194967	M	MP:0002169	no abnormal phenotype detected	Smim23<em1Osb>/Smim23<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194968	M	MP:0002169	no abnormal phenotype detected	Pinlyp<em1Osb>/Pinlyp<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194969	M	MP:0002169	no abnormal phenotype detected	Ms4a13<em1Osb>/Ms4a13<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194970	M	MP:0002169	no abnormal phenotype detected	Marchf11<em1Osb>/Marchf11<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194971	M	MP:0002169	no abnormal phenotype detected	Lyzl1<em1Osb>/Lyzl1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194972	M	MP:0002169	no abnormal phenotype detected	Kif2b<em1Osb>/Kif2b<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194973	M	MP:0002169	no abnormal phenotype detected	Gm5617<em2Osb>/Gm5617<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194974	M	MP:0002169	no abnormal phenotype detected	Gm5617<em1Osb>/Gm5617<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194975	M	MP:0002169	no abnormal phenotype detected	Fmr1nb<em1Osb>/Fmr1nb<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194976	M	MP:0002169	no abnormal phenotype detected	Fam217a<em2Osb>/Fam217a<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194977	M	MP:0002169	no abnormal phenotype detected	Fam217a<em1Osb>/Fam217a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194978	M	MP:0002169	no abnormal phenotype detected	Col20a1<em1Osb>/Col20a1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194979	M	MP:0002169	no abnormal phenotype detected	Ccdc178<em1Osb>/Ccdc178<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194980	M	MP:0002169	no abnormal phenotype detected	C1qtnf4<em1Osb>/C1qtnf4<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194981	M	MP:0002169	no abnormal phenotype detected	Selenov<em1Osb>/Selenov<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194982	M	MP:0002169	no abnormal phenotype detected	Fndc11<em1Osb>/Fndc11<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194983	M	MP:0002169	no abnormal phenotype detected	Tsbp1<em1Osb>/Tsbp1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194984	M	MP:0002169	no abnormal phenotype detected	Tex56<em1Osb>/Tex56<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194985	M	MP:0002169	no abnormal phenotype detected	Siglecl2<em1Osb>/Siglecl2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194986	M	MP:0002169	no abnormal phenotype detected	4930522H14Rik<em1Osb>/4930522H14Rik<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194987	M	MP:0002169	no abnormal phenotype detected	2900092C05Rik<em1Osb>/2900092C05Rik<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194988	M	MP:0002169	no abnormal phenotype detected	Spmip5<em1Osb>/Spmip5<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194989	M	MP:0002169	no abnormal phenotype detected	Pttg1ip2<em1Osb>/Pttg1ip2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194990	M	MP:0002169	no abnormal phenotype detected	Stpg4<em1Osb>/Stpg4<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6194991	M	MP:0002169	no abnormal phenotype detected	Spmip6<em1Osb>/Spmip6<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	27357688
MGI:6195027	M	MP:0002169	no abnormal phenotype detected	1700034J05Rik<tm1b(KOMP)Wtsi>/1700034J05Rik<tm1b(KOMP)Wtsi>	involves: 129 * BALB/c * C57BL/6N	N	27357688
MGI:6195028	M	MP:0002169	no abnormal phenotype detected	Chct1<tm1b(EUCOMM)Wtsi>/Chct1<tm1b(EUCOMM)Wtsi>	involves: 129 * BALB/c * C57BL/6N	N	27357688
MGI:6195029	M	MP:0002169	no abnormal phenotype detected	Cfap299<tm1b(EUCOMM)Wtsi>/Cfap299<tm1b(EUCOMM)Wtsi>	involves: 129 * BALB/c * C57BL/6N	N	27357688
MGI:6195030	M	MP:0002169	no abnormal phenotype detected	Smco2<tm1b(EUCOMM)Wtsi>/Smco2<tm1b(EUCOMM)Wtsi>	involves: 129 * BALB/c * C57BL/6N	N	27357688
MGI:6195031	M	MP:0002169	no abnormal phenotype detected	Spata25<tm1b(EUCOMM)Hmgu>/Spata25<tm1b(EUCOMM)Hmgu>	involves: 129 * BALB/c * C57BL/6N	N	27357688
MGI:6195032	M	MP:0002169	no abnormal phenotype detected	Saxo5<tm3b(KOMP)Wtsi>/Saxo5<tm3b(KOMP)Wtsi>	involves: 129 * BALB/c * C57BL/6N	N	27357688
MGI:6195033	M	MP:0002169	no abnormal phenotype detected	Spmap2l<tm1b(KOMP)Wtsi>/Spmap2l<tm1b(KOMP)Wtsi>	involves: 129 * BALB/c * C57BL/6N	N	27357688
MGI:6195037	M	MP:0002169	no abnormal phenotype detected	Syngr4<tm1Osb>/Syngr4<tm1Osb>	involves: C57BL/6	N	27357688
MGI:6195038	M	MP:0002169	no abnormal phenotype detected	1700093K21Rik<tm1Osb>/1700093K21Rik<tm1Osb>	involves: C57BL/6NSlc	N	27357688
MGI:6195039	M	MP:0002169	no abnormal phenotype detected	Adam18<tm1Osb>/Adam18<tm1Osb>	involves: C57BL/6	N	27357688
MGI:6195040	M	MP:0002169	no abnormal phenotype detected	Capn11<tm1Osb>/Capn11<tm1Osb>	involves: C57BL/6	N	27357688
MGI:6195041	M	MP:0002169	no abnormal phenotype detected	Lrrc36<tm1.1Osb>/Lrrc36<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	27357688
MGI:6195042	M	MP:0002169	no abnormal phenotype detected	Efcab3<tm1.1Osb>/Efcab3<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	27357688
MGI:6195043	M	MP:0002169	no abnormal phenotype detected	Lyzl4<tm1.1Osb>/Lyzl4<tm1.1Osb>	involves: 129S2/SvPas * C57BL/6NSlc * DBA/2	N	27357688
MGI:6195044	M	MP:0002169	no abnormal phenotype detected	Lyzl6<tm1.1Osb>/Lyzl6<tm1.1Osb>	involves: 129S2/SvPas * C57BL/6NSlc * DBA/2	N	27357688
MGI:6195045	M	MP:0002169	no abnormal phenotype detected	Pkdrej<tm1Osb>/Pkdrej<tm1Osb>	involves: 129S2/SvPas	N	27357688
MGI:6195047	M	MP:0002169	no abnormal phenotype detected	Spaca3<tm1Osb>/Spaca3<tm1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	27357688
MGI:6195050	M	MP:0002169	no abnormal phenotype detected	Spata4<tm1.1Osb>/Spata4<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	27357688
MGI:6195052	M	MP:0002169	no abnormal phenotype detected	Spata9<tm1Osb>/Spata9<tm1Osb>	involves: C57BL/6NSlc	N	27357688
MGI:6195053	M	MP:0002169	no abnormal phenotype detected	Spmip8<tm1.1Osb>/Spmip8<tm1.1Osb>	involves: C57BL/6 * DBA/2	N	27357688
MGI:6195054	M	MP:0002169	no abnormal phenotype detected	Tex22<tm1.1Osb>/Tex22<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	27357688
MGI:6195055	M	MP:0002169	no abnormal phenotype detected	Tsga13<tm1.1Osb>/Tsga13<tm1.1Osb>	involves: 129S2/SvPas * C57BL/6NSlc * DBA/2	N	27357688
MGI:6195056	M	MP:0002169	no abnormal phenotype detected	Zcchc13<tm1Osb>/Zcchc13<tm1Osb>	involves: C57BL/6NSlc	N	27357688
MGI:6195209	M	MP:0010926	increased osteoid volume	Ifitm5<tm1Pmof>/Ifitm5<tm1Pmof>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	28880886
MGI:6195209	F	MP:0000135	decreased compact bone thickness	Ifitm5<tm1Pmof>/Ifitm5<tm1Pmof>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	28880886
MGI:6195209	M	MP:0001262	decreased body weight	Ifitm5<tm1Pmof>/Ifitm5<tm1Pmof>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	28880886
MGI:6195209	M	MP:0000130	abnormal trabecular bone morphology	Ifitm5<tm1Pmof>/Ifitm5<tm1Pmof>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	28880886
MGI:6195209	F	MP:0003109	short femur	Ifitm5<tm1Pmof>/Ifitm5<tm1Pmof>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	28880886
MGI:6195209	F	MP:0010879	decreased trabecular bone volume	Ifitm5<tm1Pmof>/Ifitm5<tm1Pmof>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	28880886
MGI:6195209	F	MP:0013630	increased bone trabecular spacing	Ifitm5<tm1Pmof>/Ifitm5<tm1Pmof>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	28880886
MGI:6195209	F	MP:0010876	decreased bone volume	Ifitm5<tm1Pmof>/Ifitm5<tm1Pmof>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	28880886
MGI:6195209	F	MP:0010869	decreased bone trabecula number	Ifitm5<tm1Pmof>/Ifitm5<tm1Pmof>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	28880886
MGI:6195535	M	MP:0005632	decreased circulating aspartate transaminase level	Lman1<Gt(XST010)Byg>/Lman1<Gt(XST010)Byg>,Mcfd2<tm1Dgi>/Mcfd2<tm1Dgi>	B6.129-Mcfd2<tm1Dgi> Lman1<Gt(XST010)Byg>	N	29735583
MGI:6195537	M	MP:0005632	decreased circulating aspartate transaminase level	Lman1<Gt(XST010)Byg>/Lman1<Gt(XST010)Byg>	B6.129-Lman1<Gt(XST010)Byg>	N	29735583
MGI:6195539	M	MP:0005632	decreased circulating aspartate transaminase level	Mcfd2<tm1Dgi>/Mcfd2<tm1Dgi>	129S1/SvImJ-Mcfd2<tm1Dgi>	N	29735583
MGI:6195545	M	MP:0004998	decreased CNS synapse formation	Srpx2<em1Gmsa>/Y	C57BL/6J-Srpx2<em1Gmsa>	N	29920554
MGI:6195545	M	MP:0001529	abnormal vocalization	Srpx2<em1Gmsa>/Y	C57BL/6J-Srpx2<em1Gmsa>	N	29920554
MGI:6195545	M	MP:0020395	abnormal response to social novelty	Srpx2<em1Gmsa>/Y	C57BL/6J-Srpx2<em1Gmsa>	N	29920554
MGI:6195853	M	MP:0002574	increased vertical activity	Arx<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N	N	29659809
MGI:6195853	M	MP:0003491	abnormal voluntary movement	Arx<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N	N	29659809
MGI:6195853	M	MP:0003858	enhanced coordination	Arx<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N	N	29659809
MGI:6195853	M	MP:0031391	increased locomotor activity	Arx<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N	N	29659809
MGI:6195853	M	MP:0001406	abnormal gait	Arx<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N	N	29659809
MGI:6195853	M	MP:0004101	abnormal brain interneuron morphology	Arx<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N	N	29659809
MGI:6195853	M	MP:0001525	impaired balance	Arx<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N	N	29659809
MGI:6195853	M	MP:0009454	impaired contextual conditioning behavior	Arx<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N	N	29659809
MGI:6195853	M	MP:0008948	decreased neuron number	Arx<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N	N	29659809
MGI:6195853	M	MP:0006009	abnormal neuronal migration	Arx<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N	N	29659809
MGI:6195853	M	MP:0000743	muscle spasm	Arx<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N	N	29659809
MGI:6195853	M	MP:0002272	abnormal nervous system electrophysiology	Arx<tm1.1Ics>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N	N	29659809
MGI:6196013	M	MP:0002572	abnormal emotion/affect behavior	Dlgap1<tm1Grnt>/Dlgap1<tm1Grnt>	involves: 129 * C57BL/6J	N	29396406
MGI:6196014	M	MP:0001441	increased grooming behavior	Dlgap1<tm1Grnt>/Dlgap1<+>	involves: 129 * C57BL/6J	N	29396406
MGI:6196031	M	MP:0020395	abnormal response to social novelty	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0002083	premature death	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0011086	postnatal lethality, incomplete penetrance	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0012307	impaired spatial learning	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0001363	increased anxiety-related response	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0002064	seizures	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0003460	decreased fear-related response	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0001415	increased exploration in new environment	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0001360	abnormal social investigation	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0001417	decreased exploration in new environment	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0001262	decreased body weight	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0000243	myoclonus	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0002066	abnormal motor capabilities/coordination/movement	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0001402	decreased locomotor activity	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196031	M	MP:0001361	social withdrawal	Arx<tm5Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0020395	abnormal response to social novelty	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0001361	social withdrawal	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0000243	myoclonus	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0001360	abnormal social investigation	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0003460	decreased fear-related response	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0011086	postnatal lethality, incomplete penetrance	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0001415	increased exploration in new environment	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0001417	decreased exploration in new environment	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0002083	premature death	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0002066	abnormal motor capabilities/coordination/movement	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0001262	decreased body weight	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0012307	impaired spatial learning	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0001402	decreased locomotor activity	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196032	M	MP:0001363	increased anxiety-related response	Arx<tm4Kki>/Y	involves: 129S/SvEv * C57BL/6NHsd	N	28602636
MGI:6196059	F	MP:0005389	reproductive system phenotype	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	Y	29907856
MGI:6196059	M	MP:0009231	detached acrosome	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0009230	abnormal sperm head morphology	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0002687	oligozoospermia	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0001156	abnormal spermatogenesis	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0005169	abnormal male meiosis	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0002686	globozoospermia	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0009831	abnormal sperm midpiece morphology	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0001925	male infertility	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0031354	abnormal acrosome assembly	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0031386	elongated manchette	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0002675	asthenozoospermia	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0009376	abnormal manchette morphology	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0008892	abnormal sperm flagellum morphology	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0008898	abnormal acrosome morphology	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0031373	abnormal manchette perinuclear ring morphology	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0009232	abnormal sperm nucleus morphology	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0005578	teratozoospermia	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196059	M	MP:0014052	increased male germ cell apoptosis	Dcaf17<tm1.1Assi>/Dcaf17<tm1.1Assi>	involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac	N	29907856
MGI:6196101	M	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality	F9<em1Dlli>/Y	involves: C57BL/6J	N	26964564
MGI:6196101	M	MP:0012359	increased partial thromboplastin time	F9<em1Dlli>/Y	involves: C57BL/6J	N	26964564
MGI:6196104	M	MP:0005376	homeostasis/metabolism phenotype	F9<em2Dlli>/Y	involves: C57BL/6J	Y	26964564
MGI:6196105	M	MP:0002551	abnormal blood coagulation	F9<em3Dlli>/Y	involves: C57BL/6J	N	26964564
MGI:6196105	M	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality	F9<em3Dlli>/Y	involves: C57BL/6J	N	26964564
MGI:6196105	M	MP:0012359	increased partial thromboplastin time	F9<em3Dlli>/Y	involves: C57BL/6J	N	26964564
MGI:6196586	M	MP:0005281	increased fatty acids level	Abcd1<tm1Kan>/Y,Gt(ROSA)26Sor<tm2.1(CAG-ELOVL1)Geno>/Gt(ROSA)26Sor<+>,Tg(CMV-cre)1Cgn/0	involves: 129 * BALB/cJ * C57BL/6J * Swiss	N	27124591
MGI:6196586	M	MP:0010831	lethality, incomplete penetrance	Abcd1<tm1Kan>/Y,Gt(ROSA)26Sor<tm2.1(CAG-ELOVL1)Geno>/Gt(ROSA)26Sor<+>,Tg(CMV-cre)1Cgn/0	involves: 129 * BALB/cJ * C57BL/6J * Swiss	N	27124591
MGI:6196613	M	MP:0005281	increased fatty acids level	Abcd1<tm1Kan>/Y	involves: 129 * BALB/cJ * C57BL/6J * Swiss	N	27124591
MGI:6196851	M	MP:0009230	abnormal sperm head morphology	Dcun1d1<Gt(RRR261)Byg>/Dcun1d1<Gt(RRR261)Byg>	involves: 129P2/OlaHsd	N	30653527
MGI:6196851	M	MP:0003205	testicular atrophy	Dcun1d1<Gt(RRR261)Byg>/Dcun1d1<Gt(RRR261)Byg>	involves: 129P2/OlaHsd	N	30653527
MGI:6196851	M	MP:0001925	male infertility	Dcun1d1<Gt(RRR261)Byg>/Dcun1d1<Gt(RRR261)Byg>	involves: 129P2/OlaHsd	N	30653527
MGI:6196851	M	MP:0005578	teratozoospermia	Dcun1d1<Gt(RRR261)Byg>/Dcun1d1<Gt(RRR261)Byg>	involves: 129P2/OlaHsd	N	30653527
MGI:6196851	M	MP:0001154	seminiferous tubule degeneration	Dcun1d1<Gt(RRR261)Byg>/Dcun1d1<Gt(RRR261)Byg>	involves: 129P2/OlaHsd	N	30653527
MGI:6196851	M	MP:0001932	abnormal spermiogenesis	Dcun1d1<Gt(RRR261)Byg>/Dcun1d1<Gt(RRR261)Byg>	involves: 129P2/OlaHsd	N	30653527
MGI:6196851	M	MP:0001156	abnormal spermatogenesis	Dcun1d1<Gt(RRR261)Byg>/Dcun1d1<Gt(RRR261)Byg>	involves: 129P2/OlaHsd	N	30653527
MGI:6196851	M	MP:0008892	abnormal sperm flagellum morphology	Dcun1d1<Gt(RRR261)Byg>/Dcun1d1<Gt(RRR261)Byg>	involves: 129P2/OlaHsd	N	30653527
MGI:6196851	M	MP:0002686	globozoospermia	Dcun1d1<Gt(RRR261)Byg>/Dcun1d1<Gt(RRR261)Byg>	involves: 129P2/OlaHsd	N	30653527
MGI:6196851	M	MP:0002675	asthenozoospermia	Dcun1d1<Gt(RRR261)Byg>/Dcun1d1<Gt(RRR261)Byg>	involves: 129P2/OlaHsd	N	30653527
MGI:6196851	M	MP:0002687	oligozoospermia	Dcun1d1<Gt(RRR261)Byg>/Dcun1d1<Gt(RRR261)Byg>	involves: 129P2/OlaHsd	N	30653527
MGI:6197063	F	MP:0001262	decreased body weight	Atp1a3<tm1Mika>/Atp1a3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	30071271
MGI:6197218	M	MP:0000160	kyphosis	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0004144	hypotonia	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0003061	decreased aerobic running capacity	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0002106	abnormal muscle physiology	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0002108	abnormal muscle morphology	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0009413	skeletal muscle fiber atrophy	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0005292	improved glucose tolerance	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0010053	decreased grip strength	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0013278	decreased fasting circulating glucose level	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0002804	abnormal motor learning	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0005584	abnormal enzyme/coenzyme activity	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0006086	decreased body mass index	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0000747	muscle weakness	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0003960	increased lean body mass	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0010062	decreased creatine level	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0005560	decreased circulating glucose level	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0001258	decreased body length	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0001765	abnormal ion homeostasis	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0000069	kyphoscoliosis	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197218	M	MP:0001262	decreased body weight	Slc6a8<tm1e(KOMP)Wtsi>/Y	involves: C57BL/6J * C57BL/6N	N	30013483
MGI:6197239	M	MP:0001925	male infertility	Maz<em#Mhll>/Maz<em#Mhll>	C57BL/6J-Maz<em#Mhll>	N	29432158
MGI:6197239	M	MP:0003604	single kidney	Maz<em#Mhll>/Maz<em#Mhll>	C57BL/6J-Maz<em#Mhll>	N	29432158
MGI:6197239	M	MP:0003105	abnormal heart atrium morphology	Maz<em#Mhll>/Maz<em#Mhll>	C57BL/6J-Maz<em#Mhll>	N	29432158
MGI:6197473	F	MP:0004991	decreased bone strength	Tg(APCS-Tnfsf11*)#aKhs/0	C57BL/6J-Tg(APCS-Tnfsf11*)#aKhs	N	12434161
MGI:6197473	F	MP:0013639	decreased bone stiffness	Tg(APCS-Tnfsf11*)#aKhs/0	C57BL/6J-Tg(APCS-Tnfsf11*)#aKhs	N	12434161
MGI:6197473	F	MP:0000061	fragile skeleton	Tg(APCS-Tnfsf11*)#aKhs/0	C57BL/6J-Tg(APCS-Tnfsf11*)#aKhs	N	12434161
MGI:6197473	F	MP:0020010	decreased bone mineral density of femur	Tg(APCS-Tnfsf11*)#aKhs/0	C57BL/6J-Tg(APCS-Tnfsf11*)#aKhs	N	12434161
MGI:6197947	M	MP:0000746	weakness	Atad3a<tm1c(KOMP)Wtsi>/Atad3a<tm1c(KOMP)Wtsi>,Myl1<tm1(cre)Sjb>/Myl1<+>	B6J.Cg-Myl1<tm1(cre)Sjb> Atad3a<tm1c(KOMP)Wtsi>	N	29898916
MGI:6197947	M	MP:0001402	decreased locomotor activity	Atad3a<tm1c(KOMP)Wtsi>/Atad3a<tm1c(KOMP)Wtsi>,Myl1<tm1(cre)Sjb>/Myl1<+>	B6J.Cg-Myl1<tm1(cre)Sjb> Atad3a<tm1c(KOMP)Wtsi>	N	29898916
MGI:6197947	M	MP:0001516	abnormal motor coordination/balance	Atad3a<tm1c(KOMP)Wtsi>/Atad3a<tm1c(KOMP)Wtsi>,Myl1<tm1(cre)Sjb>/Myl1<+>	B6J.Cg-Myl1<tm1(cre)Sjb> Atad3a<tm1c(KOMP)Wtsi>	N	29898916
MGI:6197947	M	MP:0005150	cachexia	Atad3a<tm1c(KOMP)Wtsi>/Atad3a<tm1c(KOMP)Wtsi>,Myl1<tm1(cre)Sjb>/Myl1<+>	B6J.Cg-Myl1<tm1(cre)Sjb> Atad3a<tm1c(KOMP)Wtsi>	N	29898916
MGI:6197947	F	MP:0005150	cachexia	Atad3a<tm1c(KOMP)Wtsi>/Atad3a<tm1c(KOMP)Wtsi>,Myl1<tm1(cre)Sjb>/Myl1<+>	B6J.Cg-Myl1<tm1(cre)Sjb> Atad3a<tm1c(KOMP)Wtsi>	N	29898916
MGI:6197947	F	MP:0009413	skeletal muscle fiber atrophy	Atad3a<tm1c(KOMP)Wtsi>/Atad3a<tm1c(KOMP)Wtsi>,Myl1<tm1(cre)Sjb>/Myl1<+>	B6J.Cg-Myl1<tm1(cre)Sjb> Atad3a<tm1c(KOMP)Wtsi>	N	29898916
MGI:6197947	F	MP:0010239	decreased skeletal muscle weight	Atad3a<tm1c(KOMP)Wtsi>/Atad3a<tm1c(KOMP)Wtsi>,Myl1<tm1(cre)Sjb>/Myl1<+>	B6J.Cg-Myl1<tm1(cre)Sjb> Atad3a<tm1c(KOMP)Wtsi>	N	29898916
MGI:6198577	F	MP:0005455	increased susceptibility to weight gain	Dync1h1<tm1.1Sjki>/Dync1h1<+>	involves: 129 * 129S1/SvImJ * C57BL/6 * C57BL/6J	N	29379136
MGI:6198662	M	MP:0009413	skeletal muscle fiber atrophy	Gt(ROSA)26Sor<tm1(CAG-MFN2*T105M)Dple>/Gt(ROSA)26Sor<+>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27907123
MGI:6198662	M	MP:0003631	nervous system phenotype	Gt(ROSA)26Sor<tm1(CAG-MFN2*T105M)Dple>/Gt(ROSA)26Sor<+>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	Y	27907123
MGI:6198662	M	MP:0003084	abnormal skeletal muscle fiber morphology	Gt(ROSA)26Sor<tm1(CAG-MFN2*T105M)Dple>/Gt(ROSA)26Sor<+>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27907123
MGI:6198662	M	MP:0001407	short stride length	Gt(ROSA)26Sor<tm1(CAG-MFN2*T105M)Dple>/Gt(ROSA)26Sor<+>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27907123
MGI:6198662	M	MP:0009409	abnormal skeletal muscle fiber type ratio	Gt(ROSA)26Sor<tm1(CAG-MFN2*T105M)Dple>/Gt(ROSA)26Sor<+>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27907123
MGI:6198662	M	MP:0011629	decreased mitochondrial number	Gt(ROSA)26Sor<tm1(CAG-MFN2*T105M)Dple>/Gt(ROSA)26Sor<+>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27907123
MGI:6198662	M	MP:0009402	decreased skeletal muscle fiber diameter	Gt(ROSA)26Sor<tm1(CAG-MFN2*T105M)Dple>/Gt(ROSA)26Sor<+>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27907123
MGI:6198662	M	MP:0003081	abnormal soleus morphology	Gt(ROSA)26Sor<tm1(CAG-MFN2*T105M)Dple>/Gt(ROSA)26Sor<+>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	27907123
MGI:6198725	M	MP:0002986	decreased urine calcium level	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198725	M	MP:0000198	decreased circulating phosphate level	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198725	M	MP:0031060	decreased circulating C-reactive protein level	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198725	M	MP:0000063	decreased bone mineral density	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198725	M	MP:0005385	cardiovascular system phenotype	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	Y	29735309
MGI:6198725	M	MP:0005367	renal/urinary system phenotype	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	Y	29735309
MGI:6198725	M	MP:0009642	abnormal blood homeostasis	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198725	M	MP:0012336	decreased vitamin D level	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198725	M	MP:0002904	increased circulating parathyroid hormone level	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198725	M	MP:0003620	oliguria	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198725	M	MP:0005370	liver/biliary system phenotype	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	Y	29735309
MGI:6198725	M	MP:0011470	increased urine creatinine level	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198725	M	MP:0003432	increased activity of parathyroid	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198725	M	MP:0003797	abnormal compact bone morphology	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198725	M	MP:0006264	decreased systemic arterial systolic blood pressure	Phex<Mhdabap024>/Y	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198726	F	MP:0000198	decreased circulating phosphate level	Phex<Mhdabap024>/Phex<+>	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198726	F	MP:0009642	abnormal blood homeostasis	Phex<Mhdabap024>/Phex<+>	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198726	F	MP:0002904	increased circulating parathyroid hormone level	Phex<Mhdabap024>/Phex<+>	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198726	F	MP:0003432	increased activity of parathyroid	Phex<Mhdabap024>/Phex<+>	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198726	F	MP:0002901	increased urine phosphate level	Phex<Mhdabap024>/Phex<+>	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198726	F	MP:0005385	cardiovascular system phenotype	Phex<Mhdabap024>/Phex<+>	C3HeB/FeJ-Phex<Mhdabap024>	Y	29735309
MGI:6198726	F	MP:0005367	renal/urinary system phenotype	Phex<Mhdabap024>/Phex<+>	C3HeB/FeJ-Phex<Mhdabap024>	Y	29735309
MGI:6198726	F	MP:0002986	decreased urine calcium level	Phex<Mhdabap024>/Phex<+>	C3HeB/FeJ-Phex<Mhdabap024>	N	29735309
MGI:6198765	M	MP:0001158	abnormal prostate gland morphology	Tg(CAG-MYC,-GFP*)#Rugg/0,Tg(Pbsn-cre)4Prb/0	involves: C57BL/6 * C57BL/6J * DBA/2	N	29720449
MGI:6198765	M	MP:0002006	neoplasm	Tg(CAG-MYC,-GFP*)#Rugg/0,Tg(Pbsn-cre)4Prb/0	involves: C57BL/6 * C57BL/6J * DBA/2	Y	29720449
MGI:6198766	M	MP:0002083	premature death	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CAG-MYC,-GFP*)#Rugg/0,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2	N	29720449
MGI:6198766	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CAG-MYC,-GFP*)#Rugg/0,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2	N	29720449
MGI:6198766	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CAG-MYC,-GFP*)#Rugg/0,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2	N	29720449
MGI:6198768	M	MP:0012432	decreased prostate gland tumor incidence	Eif2ak3<tm1.2Drc>/Eif2ak3<tm1.2Drc>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(CAG-MYC,-GFP*)#Rugg/0,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J * DBA/2	N	29720449
MGI:6199038	M	MP:0009454	impaired contextual conditioning behavior	Grn<tm1.1Hiok>/Grn<+>	involves: C57BL/6J	N	29382817
MGI:6199038	M	MP:0001405	impaired coordination	Grn<tm1.1Hiok>/Grn<+>	involves: C57BL/6J	N	29382817
MGI:6199038	M	MP:0008432	abnormal long-term spatial reference memory	Grn<tm1.1Hiok>/Grn<+>	involves: C57BL/6J	N	29382817
MGI:6200082	F	MP:0001931	abnormal oogenesis	Patl2<tm1b(EUCOMM)Hmgu>/Patl2<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB/N	N	29661911
MGI:6200082	F	MP:0000242	impaired fertilization	Patl2<tm1b(EUCOMM)Hmgu>/Patl2<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB/N	N	29661911
MGI:6200082	F	MP:0001923	reduced female fertility	Patl2<tm1b(EUCOMM)Hmgu>/Patl2<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB/N	N	29661911
MGI:6200082	F	MP:0011120	increased primordial ovarian follicle number	Patl2<tm1b(EUCOMM)Hmgu>/Patl2<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB/N	N	29661911
MGI:6200082	F	MP:0010767	abnormal female meiosis I arrest	Patl2<tm1b(EUCOMM)Hmgu>/Patl2<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB/N	N	29661911
MGI:6200082	F	MP:0014447	impaired spindle assembly in female meiosis	Patl2<tm1b(EUCOMM)Hmgu>/Patl2<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB/N	N	29661911
MGI:6200082	F	MP:0005168	abnormal female meiosis	Patl2<tm1b(EUCOMM)Hmgu>/Patl2<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB/N	N	29661911
MGI:6200082	F	MP:0031014	polyspermy	Patl2<tm1b(EUCOMM)Hmgu>/Patl2<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB/N	N	29661911
MGI:6200082	F	MP:0001125	abnormal oocyte morphology	Patl2<tm1b(EUCOMM)Hmgu>/Patl2<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB/N	N	29661911
MGI:6200082	F	MP:0001935	decreased litter size	Patl2<tm1b(EUCOMM)Hmgu>/Patl2<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB/N	N	29661911
MGI:6200082	F	MP:0009761	abnormal meiotic spindle morphology	Patl2<tm1b(EUCOMM)Hmgu>/Patl2<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB/N	N	29661911
MGI:6200082	M	MP:0005389	reproductive system phenotype	Patl2<tm1b(EUCOMM)Hmgu>/Patl2<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB/N	Y	29661911
MGI:6200722	F	MP:0001218	thin epidermis	Eda<Ta>/Eda<Ta>	B6.Cg-A<w-J> Eda<Ta>/JGbms	N	7544943
MGI:6200722	F	MP:0003704	abnormal hair follicle development	Eda<Ta>/Eda<Ta>	B6.Cg-A<w-J> Eda<Ta>/JGbms	N	7544943
MGI:6200790	M	MP:0009234	absent sperm head	Spatc1l<em1Choc>/Spatc1l<em1Choc>	involves: C57BL/6J * C57BL/6N	N	30026308
MGI:6200790	M	MP:0001925	male infertility	Spatc1l<em1Choc>/Spatc1l<em1Choc>	involves: C57BL/6J * C57BL/6N	N	30026308
MGI:6200790	M	MP:0005578	teratozoospermia	Spatc1l<em1Choc>/Spatc1l<em1Choc>	involves: C57BL/6J * C57BL/6N	N	30026308
MGI:6200790	M	MP:0008893	detached sperm flagellum	Spatc1l<em1Choc>/Spatc1l<em1Choc>	involves: C57BL/6J * C57BL/6N	N	30026308
MGI:6200791	M	MP:0008545	absent sperm flagellum	Spatc1l<em1Choc>/Spatc1l<+>	involves: C57BL/6J * C57BL/6N	N	30026308
MGI:6200791	M	MP:0001922	reduced male fertility	Spatc1l<em1Choc>/Spatc1l<+>	involves: C57BL/6J * C57BL/6N	N	30026308
MGI:6200791	F	MP:0005389	reproductive system phenotype	Spatc1l<em1Choc>/Spatc1l<+>	involves: C57BL/6J * C57BL/6N	Y	30026308
MGI:6200791	M	MP:0009230	abnormal sperm head morphology	Spatc1l<em1Choc>/Spatc1l<+>	involves: C57BL/6J * C57BL/6N	N	30026308
MGI:6201236	M	MP:0009422	decreased gastrocnemius weight	Dctn1<tm2.1Cai>/Dctn1<tm2.1Cai>,Tg(Thy1-cre)1Vln/?	involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * FVB/N	N	29490687
MGI:6201426	M	MP:0010378	increased respiratory quotient	Zbed6<tm1.2Sson>/Zbed6<tm1.2Sson>	involves: BALB/c * C57BL/6	N	29440408
MGI:6201426	M	MP:0002891	increased insulin sensitivity	Zbed6<tm1.2Sson>/Zbed6<tm1.2Sson>	involves: BALB/c * C57BL/6	N	29440408
MGI:6201426	F	MP:0002981	increased liver weight	Zbed6<tm1.2Sson>/Zbed6<tm1.2Sson>	involves: BALB/c * C57BL/6	N	29440408
MGI:6201426	F	MP:0003960	increased lean body mass	Zbed6<tm1.2Sson>/Zbed6<tm1.2Sson>	involves: BALB/c * C57BL/6	N	29440408
MGI:6201426	F	MP:0003398	increased skeletal muscle size	Zbed6<tm1.2Sson>/Zbed6<tm1.2Sson>	involves: BALB/c * C57BL/6	N	29440408
MGI:6201427	M	MP:0010378	increased respiratory quotient	Rr143<tm1.1Sson>/Rr143<+>,Zbed6<tm1.2Sson>/Zbed6<tm1.2Sson>	involves: BALB/c * C57BL/6	N	29440408
MGI:6201427	F	MP:0003398	increased skeletal muscle size	Rr143<tm1.1Sson>/Rr143<+>,Zbed6<tm1.2Sson>/Zbed6<tm1.2Sson>	involves: BALB/c * C57BL/6	N	29440408
MGI:6201427	F	MP:0002981	increased liver weight	Rr143<tm1.1Sson>/Rr143<+>,Zbed6<tm1.2Sson>/Zbed6<tm1.2Sson>	involves: BALB/c * C57BL/6	N	29440408
MGI:6201427	F	MP:0003960	increased lean body mass	Rr143<tm1.1Sson>/Rr143<+>,Zbed6<tm1.2Sson>/Zbed6<tm1.2Sson>	involves: BALB/c * C57BL/6	N	29440408
MGI:6201428	F	MP:0002833	increased heart weight	Rr143<tm1.1Sson>/Rr143<+>	involves: BALB/c * C57BL/6	N	29440408
MGI:6201521	M	MP:0001925	male infertility	Fbxo43<tm1.1Kald>/Fbxo43<tm1.2Kald>,Gt(ROSA)26Sor<tm1(cre/ERT)Brn>/Gt(ROSA)26Sor<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201521	M	MP:0014052	increased male germ cell apoptosis	Fbxo43<tm1.1Kald>/Fbxo43<tm1.2Kald>,Gt(ROSA)26Sor<tm1(cre/ERT)Brn>/Gt(ROSA)26Sor<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201523	M	MP:0014052	increased male germ cell apoptosis	Fbxo43<tm1.1Kald>/Fbxo43<tm1.1Kald>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	28723571
MGI:6201523	M	MP:0001925	male infertility	Fbxo43<tm1.1Kald>/Fbxo43<tm1.1Kald>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	28723571
MGI:6201523	M	MP:0008261	arrest of male meiosis	Fbxo43<tm1.1Kald>/Fbxo43<tm1.1Kald>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	28723571
MGI:6201524	M	MP:0014052	increased male germ cell apoptosis	Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>	involves: 129 * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201524	F	MP:0002006	neoplasm	Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>	involves: 129 * C57BL/6 * FVB/N * SJL	Y	28723571
MGI:6201524	M	MP:0004852	decreased testis weight	Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>	involves: 129 * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201524	F	MP:0001926	female infertility	Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>	involves: 129 * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201524	M	MP:0001925	male infertility	Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>	involves: 129 * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201524	M	MP:0005159	azoospermia	Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>	involves: 129 * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201524	F	MP:0005168	abnormal female meiosis	Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>	involves: 129 * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201524	M	MP:0008261	arrest of male meiosis	Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>	involves: 129 * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201524	F	MP:0001125	abnormal oocyte morphology	Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>	involves: 129 * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201524	F	MP:0009443	parthenogenesis	Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>	involves: 129 * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201524	M	MP:0001147	small testis	Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>	involves: 129 * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201526	M	MP:0008261	arrest of male meiosis	Cdk1<tm3Kald>/Cdk1<+>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ	N	28723571
MGI:6201526	M	MP:0005159	azoospermia	Cdk1<tm3Kald>/Cdk1<+>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ	N	28723571
MGI:6201526	M	MP:0001147	small testis	Cdk1<tm3Kald>/Cdk1<+>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ	N	28723571
MGI:6201527	M	MP:0005159	azoospermia	Cdk1<tm3Kald>/Cdk1<+>,Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>,Gt(ROSA)26Sor<tm1(cre/ERT)Brn>/Gt(ROSA)26Sor<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201527	M	MP:0008261	arrest of male meiosis	Cdk1<tm3Kald>/Cdk1<+>,Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>,Gt(ROSA)26Sor<tm1(cre/ERT)Brn>/Gt(ROSA)26Sor<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6201527	M	MP:0014052	increased male germ cell apoptosis	Cdk1<tm3Kald>/Cdk1<+>,Fbxo43<tm1.2Kald>/Fbxo43<tm1.2Kald>,Gt(ROSA)26Sor<tm1(cre/ERT)Brn>/Gt(ROSA)26Sor<+>	involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	N	28723571
MGI:6202041	M	MP:0011774	abnormal urinary bladder detrusor smooth muscle morphology	Slc3a1<tm1Jat>/Slc3a1<tm1Jat>	involves: 129 * C57BL/6	N	19484501
MGI:6202041	F	MP:0001756	abnormal urination	Slc3a1<tm1Jat>/Slc3a1<tm1Jat>	involves: 129 * C57BL/6	N	19484501
MGI:6202041	M	MP:0003587	ureter obstruction	Slc3a1<tm1Jat>/Slc3a1<tm1Jat>	involves: 129 * C57BL/6	N	19484501
MGI:6202041	M	MP:0020400	cystinuria	Slc3a1<tm1Jat>/Slc3a1<tm1Jat>	involves: 129 * C57BL/6	N	28165480
MGI:6202041	M	MP:0011799	increased urinary bladder weight	Slc3a1<tm1Jat>/Slc3a1<tm1Jat>	involves: 129 * C57BL/6	N	19484501
MGI:6202041	M	MP:0011625	cystolithiasis	Slc3a1<tm1Jat>/Slc3a1<tm1Jat>	involves: 129 * C57BL/6	N	28165480
MGI:6202041	M	MP:0002708	nephrolithiasis	Slc3a1<tm1Jat>/Slc3a1<tm1Jat>	involves: 129 * C57BL/6	N	19484501
MGI:6202041	M	MP:0011625	cystolithiasis	Slc3a1<tm1Jat>/Slc3a1<tm1Jat>	involves: 129 * C57BL/6	N	19484501
MGI:6202582	M	MP:0003704	abnormal hair follicle development	Eda<Ta>/Y	B6.Cg-A<w-J> Eda<Ta>/JGbms	N	7544943
MGI:6202582	M	MP:0001218	thin epidermis	Eda<Ta>/Y	B6.Cg-A<w-J> Eda<Ta>/JGbms	N	7544943
MGI:6203626	M	MP:0006362	abnormal male germ cell morphology	Haspin<tm1Htan>/Haspin<tm1Htan>	involves: C57BL/6	N	27389782
MGI:6209392	F	MP:0020351	decreased vocalization	Slc9a9<tm1.1Yzj>/Slc9a9<tm1.1Yzj>	Not Specified	N	26755066
MGI:6209426	M	MP:0009387	abnormal epidermal pigmentation	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2	N	25290687
MGI:6209426	M	MP:0010741	abnormal melanocyte proliferation	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2	N	25290687
MGI:6209426	M	MP:0011277	decreased tail pigmentation	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2	N	25290687
MGI:6209426	M	MP:0011632	dilated mitochondrion	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2	N	25290687
MGI:6209426	M	MP:0003674	oxidative stress	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2	N	25290687
MGI:6209426	M	MP:0002075	abnormal coat/hair pigmentation	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2	N	25290687
MGI:6209426	M	MP:0009388	abnormal epidermal melanocyte morphology	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2	N	25290687
MGI:6209426	M	MP:0008260	abnormal autophagy	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2	N	25290687
MGI:6209426	M	MP:0005075	abnormal melanosome morphology	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2	N	25290687
MGI:6209426	M	MP:0011568	decreased foot pigmentation	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2	N	25290687
MGI:6209426	M	MP:0008008	early cellular replicative senescence	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2	N	25290687
MGI:6209687	M	MP:0000880	decreased Purkinje cell number	Slc9a6<tm1Tigm>/Y	B6J.Cg-Slc9a6<tm1Tigm>	N	29349289
MGI:6214840	M	MP:0006264	decreased systemic arterial systolic blood pressure	Wnk4<tm3.1Suc>/Wnk4<tm3.1Suc>	involves: 129S4/SvJae * C57BL/6J	N	24655003
MGI:6220632	M	MP:0008732	reduced hair shaft melanin granule number	Zeb2<tm1.1Yhi>/Zeb2<tm1.1Yhi>,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	24769727
MGI:6220632	M	MP:0005408	hypopigmentation	Zeb2<tm1.1Yhi>/Zeb2<tm1.1Yhi>,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	24769727
MGI:6220636	M	MP:0009784	abnormal melanoblast migration	Zeb2<tm1.1Yhi>/Zeb2<tm1.1Yhi>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * DBA/2	N	24769727
MGI:6220636	M	MP:0009759	abnormal hair follicle bulge morphology	Zeb2<tm1.1Yhi>/Zeb2<tm1.1Yhi>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * DBA/2	N	24769727
MGI:6220636	M	MP:0004381	abnormal hair follicle melanocyte morphology	Zeb2<tm1.1Yhi>/Zeb2<tm1.1Yhi>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * DBA/2	N	24769727
MGI:6220636	M	MP:0009783	abnormal melanoblast morphology	Zeb2<tm1.1Yhi>/Zeb2<tm1.1Yhi>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * DBA/2	N	24769727
MGI:6220636	M	MP:0005075	abnormal melanosome morphology	Zeb2<tm1.1Yhi>/Zeb2<tm1.1Yhi>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * DBA/2	N	24769727
MGI:6220636	M	MP:0000394	absent hair follicle melanin granules	Zeb2<tm1.1Yhi>/Zeb2<tm1.1Yhi>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * DBA/2	N	24769727
MGI:6220636	M	MP:0008732	reduced hair shaft melanin granule number	Zeb2<tm1.1Yhi>/Zeb2<tm1.1Yhi>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * DBA/2	N	24769727
MGI:6220867	M	MP:0009388	abnormal epidermal melanocyte morphology	Chek1<tm1Jmr>/Chek1<tm1Jmr>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * DBA/2	N	23557358
MGI:6220867	M	MP:0004381	abnormal hair follicle melanocyte morphology	Chek1<tm1Jmr>/Chek1<tm1Jmr>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * DBA/2	N	23557358
MGI:6220867	M	MP:0012023	decreased melanocyte number	Chek1<tm1Jmr>/Chek1<tm1Jmr>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * DBA/2	N	23557358
MGI:6220867	M	MP:0005171	absent coat pigmentation	Chek1<tm1Jmr>/Chek1<tm1Jmr>,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * DBA/2	N	23557358
MGI:6220868	M	MP:0009783	abnormal melanoblast morphology	Chek1<tm1Jmr>/Chek1<tm1Jmr>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * CBA * DBA/2	N	23557358
MGI:6220868	M	MP:0008057	abnormal DNA replication	Chek1<tm1Jmr>/Chek1<tm1Jmr>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * CBA * DBA/2	N	23557358
MGI:6220869	M	MP:0009783	abnormal melanoblast morphology	Chek1<tm1Jmr>/Chek1<+>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * CBA * DBA/2	N	23557358
MGI:6220869	M	MP:0001186	pigmentation phenotype	Chek1<tm1Jmr>/Chek1<+>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: C57BL/6 * CBA * DBA/2	Y	23557358
MGI:6226058	M	MP:0002075	abnormal coat/hair pigmentation	Yy1<tm2.1Yshi>/Yy1<tm2.1Yshi>,Tg(Tyr-cre)1Lru/Y	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22570637
MGI:6226058	M	MP:0012023	decreased melanocyte number	Yy1<tm2.1Yshi>/Yy1<tm2.1Yshi>,Tg(Tyr-cre)1Lru/Y	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22570637
MGI:6226058	M	MP:0000394	absent hair follicle melanin granules	Yy1<tm2.1Yshi>/Yy1<tm2.1Yshi>,Tg(Tyr-cre)1Lru/Y	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22570637
MGI:6226058	M	MP:0005072	abnormal hair follicle melanin granule morphology	Yy1<tm2.1Yshi>/Yy1<tm2.1Yshi>,Tg(Tyr-cre)1Lru/Y	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22570637
MGI:6226058	M	MP:0008238	abnormal dorsoventral coat patterning	Yy1<tm2.1Yshi>/Yy1<tm2.1Yshi>,Tg(Tyr-cre)1Lru/Y	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22570637
MGI:6226058	M	MP:0011627	decreased skin pigmentation	Yy1<tm2.1Yshi>/Yy1<tm2.1Yshi>,Tg(Tyr-cre)1Lru/Y	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22570637
MGI:6226058	M	MP:0004381	abnormal hair follicle melanocyte morphology	Yy1<tm2.1Yshi>/Yy1<tm2.1Yshi>,Tg(Tyr-cre)1Lru/Y	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	22570637
MGI:6226060	M	MP:0000394	absent hair follicle melanin granules	Yy1<tm2.1Yshi>/Yy1<tm2.1Yshi>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: 129S4/SvJae * C57BL/6 * CBA * DBA/2	N	22570637
MGI:6226060	M	MP:0009783	abnormal melanoblast morphology	Yy1<tm2.1Yshi>/Yy1<tm2.1Yshi>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: 129S4/SvJae * C57BL/6 * CBA * DBA/2	N	22570637
MGI:6226060	M	MP:0004381	abnormal hair follicle melanocyte morphology	Yy1<tm2.1Yshi>/Yy1<tm2.1Yshi>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: 129S4/SvJae * C57BL/6 * CBA * DBA/2	N	22570637
MGI:6226060	M	MP:0012023	decreased melanocyte number	Yy1<tm2.1Yshi>/Yy1<tm2.1Yshi>,Tg(Dct-lacZ)A12Jkn/0,Tg(Tyr-cre)1Lru/Y	involves: 129S4/SvJae * C57BL/6 * CBA * DBA/2	N	22570637
MGI:6231210	F	MP:0002026	increased leukemia incidence	Tg(H2-K-Hmga1)#Lmsr/0	involves: C57BL/6 * SJL	N	17483309
MGI:6231210	F	MP:0001926	female infertility	Tg(H2-K-Hmga1)#Lmsr/0	involves: C57BL/6 * SJL	N	17483309
MGI:6231210	F	MP:0012431	increased lymphoma incidence	Tg(H2-K-Hmga1)#Lmsr/0	involves: C57BL/6 * SJL	N	17483309
MGI:6231210	F	MP:0009222	increased uterus tumor incidence	Tg(H2-K-Hmga1)#Lmsr/0	involves: C57BL/6 * SJL	N	17483309
MGI:6231210	F	MP:0001135	abnormal uterine cervix morphology	Tg(H2-K-Hmga1)#Lmsr/0	involves: C57BL/6 * SJL	N	15150086
MGI:6231210	F	MP:0003570	increased uterus leiomyoma incidence	Tg(H2-K-Hmga1)#Lmsr/0	involves: C57BL/6 * SJL	N	17483309
MGI:6231210	F	MP:0004896	abnormal endometrium morphology	Tg(H2-K-Hmga1)#Lmsr/0	involves: C57BL/6 * SJL	N	17483309
MGI:6236288	F	MP:0002169	no abnormal phenotype detected	Rragb<tm1.1Dmsa>/Rragb<tm1.1Dmsa>	involves: 129S4/SvJae * C57BL/6	N	24768164
MGI:6236290	M	MP:0002169	no abnormal phenotype detected	Rragb<tm1.1Dmsa>/Y	involves: 129S4/SvJae * C57BL/6	N	24768164
MGI:6241367	M	MP:0030590	abnormal sperm fibrous sheath morphology	Rsph6a<em1Osb>/Rsph6a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30185526
MGI:6241367	M	MP:0031375	abnormal manchette disassembly	Rsph6a<em1Osb>/Rsph6a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30185526
MGI:6241367	M	MP:0001925	male infertility	Rsph6a<em1Osb>/Rsph6a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30185526
MGI:6241367	M	MP:0009838	abnormal sperm axoneme morphology	Rsph6a<em1Osb>/Rsph6a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30185526
MGI:6241367	M	MP:0009230	abnormal sperm head morphology	Rsph6a<em1Osb>/Rsph6a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30185526
MGI:6241367	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Rsph6a<em1Osb>/Rsph6a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30185526
MGI:6241367	M	MP:0020869	immotile sperm	Rsph6a<em1Osb>/Rsph6a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30185526
MGI:6241367	M	MP:0009239	short sperm flagellum	Rsph6a<em1Osb>/Rsph6a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30185526
MGI:6241367	M	MP:0001156	abnormal spermatogenesis	Rsph6a<em1Osb>/Rsph6a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30185526
MGI:6241368	M	MP:0020869	immotile sperm	Rsph6a<em2Osb>/Rsph6a<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30185526
MGI:6241368	M	MP:0009230	abnormal sperm head morphology	Rsph6a<em2Osb>/Rsph6a<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30185526
MGI:6241368	M	MP:0009239	short sperm flagellum	Rsph6a<em2Osb>/Rsph6a<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30185526
MGI:6241517	M	MP:0001186	pigmentation phenotype	Rest<tm1.1Yasu>/Rest<+>,Tg(Tyr-cre)1Lru/Y	involves: 129S4/SvJae * C57BL/6 * DBA/2	Y	25818501
MGI:6241524	M	MP:0001186	pigmentation phenotype	Rest<tm1.1Yasu>/Rest<tm1.1Yasu>,Tg(Tyr-cre)1Lru/Y	involves: 129S4/SvJae * C57BL/6 * DBA/2	Y	25818501
MGI:6246602	F	MP:0010831	lethality, incomplete penetrance	Trp53<tm1.1Hwan>/Trp53<tm1.1Hwan>	involves: C57BL/6 * C57BL/6N	N	30042151
MGI:6251493	M	MP:0020290	floppy ears	Edil3<Tg(lacZ)1Tq>/Edil3<Tg(lacZ)1Tq>	Not Specified	N	27505251
MGI:6251493	M	MP:0003724	increased susceptibility to induced arthritis	Edil3<Tg(lacZ)1Tq>/Edil3<Tg(lacZ)1Tq>	Not Specified	N	27505251
MGI:6251493	M	MP:0006433	abnormal articular cartilage morphology	Edil3<Tg(lacZ)1Tq>/Edil3<Tg(lacZ)1Tq>	Not Specified	N	27505251
MGI:6251493	M	MP:0030423	abnormal pinna cartilage morphology	Edil3<Tg(lacZ)1Tq>/Edil3<Tg(lacZ)1Tq>	Not Specified	N	27505251
MGI:6251493	M	MP:0014103	increased chondrocyte apoptosis	Edil3<Tg(lacZ)1Tq>/Edil3<Tg(lacZ)1Tq>	Not Specified	N	27505251
MGI:6251493	M	MP:0008873	increased physiological sensitivity to xenobiotic	Edil3<Tg(lacZ)1Tq>/Edil3<Tg(lacZ)1Tq>	Not Specified	N	27505251
MGI:6251493	M	MP:0005390	skeleton phenotype	Edil3<Tg(lacZ)1Tq>/Edil3<Tg(lacZ)1Tq>	Not Specified	Y	27505251
MGI:6258254	M	MP:0010207	abnormal telomere morphology	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0008866	chromosomal instability	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0008402	increased cellular sensitivity to alkylating agents	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0003786	premature aging	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0009704	increased skin squamous cell carcinoma incidence	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0001221	epidermal atrophy	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0001214	skin hyperplasia	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0013488	increased keratoacanthoma incidence	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0009387	abnormal epidermal pigmentation	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0010300	increased skin tumor incidence	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0001203	increased sensitivity to skin irradiation	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0004030	induced chromosome breakage	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0002060	abnormal skin morphology	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0003413	hair follicle degeneration	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0010202	focal dorsal hair loss	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0011101	prenatal lethality, incomplete penetrance	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0003853	dry skin	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0001202	skin photosensitivity	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0009584	decreased keratinocyte proliferation	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0000649	sebaceous gland atrophy	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0008058	abnormal DNA repair	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0008410	increased cellular sensitivity to ultraviolet irradiation	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0030927	decreased telomere length	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0003453	abnormal keratinocyte physiology	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0030926	increased skin pigmentation	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0004501	increased incidence of tumors by UV-induction	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0030051	increased foot pigmentation	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0011278	increased ear pigmentation	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0001222	epidermal hyperplasia	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258254	M	MP:0011276	increased tail pigmentation	Tg(KRT5-Terf2)PMBlas/Y	involves: C57BL/6 * CBA	N	16142233
MGI:6258445	M	MP:0014052	increased male germ cell apoptosis	Sox30<em2Hncs>/Sox30<em2Hncs>	involves: C57BL/6J * DBA * ICR	N	29848638
MGI:6258445	M	MP:0001925	male infertility	Sox30<em2Hncs>/Sox30<em2Hncs>	involves: C57BL/6J * DBA * ICR	N	29848638
MGI:6258445	M	MP:0004930	small epididymis	Sox30<em2Hncs>/Sox30<em2Hncs>	involves: C57BL/6J * DBA * ICR	N	29848638
MGI:6258445	M	MP:0001155	arrest of spermatogenesis	Sox30<em2Hncs>/Sox30<em2Hncs>	involves: C57BL/6J * DBA * ICR	N	29848638
MGI:6258445	M	MP:0001147	small testis	Sox30<em2Hncs>/Sox30<em2Hncs>	involves: C57BL/6J * DBA * ICR	N	29848638
MGI:6258677	M	MP:0008732	reduced hair shaft melanin granule number	Acvr2a<tm1Hsch>/Acvr2a<tm1Hsch>,Bmpr2<tm1.1Enl>/Bmpr2<tm1.1Enl>,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2	N	22611050
MGI:6258677	M	MP:0000371	diluted coat color	Acvr2a<tm1Hsch>/Acvr2a<tm1Hsch>,Bmpr2<tm1.1Enl>/Bmpr2<tm1.1Enl>,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2	N	22611050
MGI:6258677	M	MP:0005072	abnormal hair follicle melanin granule morphology	Acvr2a<tm1Hsch>/Acvr2a<tm1Hsch>,Bmpr2<tm1.1Enl>/Bmpr2<tm1.1Enl>,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2	N	22611050
MGI:6258677	M	MP:0030918	small melanosome	Acvr2a<tm1Hsch>/Acvr2a<tm1Hsch>,Bmpr2<tm1.1Enl>/Bmpr2<tm1.1Enl>,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2	N	22611050
MGI:6258677	M	MP:0002075	abnormal coat/hair pigmentation	Acvr2a<tm1Hsch>/Acvr2a<tm1Hsch>,Bmpr2<tm1.1Enl>/Bmpr2<tm1.1Enl>,Tg(Tyr-cre)1Lru/Y	involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2	N	22611050
MGI:6258685	F	MP:0010389	mosaic coat color	Acvr2a<tm1Hsch>/Acvr2a<tm1Hsch>,Bmpr2<tm1.1Enl>/Bmpr2<tm1.1Enl>,Tg(Tyr-cre)1Lru/0	involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2	N	22611050
MGI:6258771	M	MP:0001380	reduced male mating frequency	Grin1<tm1Bhk>/Grin1<tm1Bhk>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22726567
MGI:6258771	M	MP:0020351	decreased vocalization	Grin1<tm1Bhk>/Grin1<tm1Bhk>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22726567
MGI:6258771	M	MP:0001513	limb grasping	Grin1<tm1Bhk>/Grin1<tm1Bhk>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22726567
MGI:6258771	M	MP:0008428	abnormal spatial working memory	Grin1<tm1Bhk>/Grin1<tm1Bhk>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22726567
MGI:6258771	M	MP:0001488	increased startle reflex	Grin1<tm1Bhk>/Grin1<tm1Bhk>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22726567
MGI:6258771	M	MP:0006335	abnormal hearing electrophysiology	Grin1<tm1Bhk>/Grin1<tm1Bhk>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22726567
MGI:6258771	M	MP:0009142	decreased prepulse inhibition	Grin1<tm1Bhk>/Grin1<tm1Bhk>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22726567
MGI:6258771	M	MP:0001441	increased grooming behavior	Grin1<tm1Bhk>/Grin1<tm1Bhk>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22726567
MGI:6258771	M	MP:0031391	increased locomotor activity	Grin1<tm1Bhk>/Grin1<tm1Bhk>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22726567
MGI:6258771	M	MP:0001360	abnormal social investigation	Grin1<tm1Bhk>/Grin1<tm1Bhk>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22726567
MGI:6258771	M	MP:0004738	abnormal auditory brainstem response	Grin1<tm1Bhk>/Grin1<tm1Bhk>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	N	22726567
MGI:6258951	M	MP:0002662	abnormal cauda epididymis morphology	Cfap44<em1Fzh>/Cfap44<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258951	M	MP:0031356	abnormal outer dense fiber morphology	Cfap44<em1Fzh>/Cfap44<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258951	M	MP:0008545	absent sperm flagellum	Cfap44<em1Fzh>/Cfap44<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258951	M	MP:0001925	male infertility	Cfap44<em1Fzh>/Cfap44<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258951	M	MP:0002687	oligozoospermia	Cfap44<em1Fzh>/Cfap44<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258951	M	MP:0009238	coiled sperm flagellum	Cfap44<em1Fzh>/Cfap44<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258951	M	MP:0002675	asthenozoospermia	Cfap44<em1Fzh>/Cfap44<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258951	M	MP:0009838	abnormal sperm axoneme morphology	Cfap44<em1Fzh>/Cfap44<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258951	M	MP:0009239	short sperm flagellum	Cfap44<em1Fzh>/Cfap44<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258951	M	MP:0009237	kinked sperm flagellum	Cfap44<em1Fzh>/Cfap44<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258951	M	MP:0008892	abnormal sperm flagellum morphology	Cfap44<em1Fzh>/Cfap44<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258951	M	MP:0031352	absent sperm axonemal central pair	Cfap44<em1Fzh>/Cfap44<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258952	M	MP:0009237	kinked sperm flagellum	Cfap43<em1Fzh>/Cfap43<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258952	M	MP:0002687	oligozoospermia	Cfap43<em1Fzh>/Cfap43<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258952	M	MP:0031356	abnormal outer dense fiber morphology	Cfap43<em1Fzh>/Cfap43<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258952	M	MP:0031352	absent sperm axonemal central pair	Cfap43<em1Fzh>/Cfap43<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258952	M	MP:0002662	abnormal cauda epididymis morphology	Cfap43<em1Fzh>/Cfap43<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258952	M	MP:0009238	coiled sperm flagellum	Cfap43<em1Fzh>/Cfap43<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258952	M	MP:0009239	short sperm flagellum	Cfap43<em1Fzh>/Cfap43<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258952	M	MP:0031351	abnormal sperm flagellum thickness	Cfap43<em1Fzh>/Cfap43<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258952	M	MP:0002675	asthenozoospermia	Cfap43<em1Fzh>/Cfap43<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258952	M	MP:0009838	abnormal sperm axoneme morphology	Cfap43<em1Fzh>/Cfap43<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258952	M	MP:0008892	abnormal sperm flagellum morphology	Cfap43<em1Fzh>/Cfap43<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258952	M	MP:0001925	male infertility	Cfap43<em1Fzh>/Cfap43<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258952	M	MP:0008545	absent sperm flagellum	Cfap43<em1Fzh>/Cfap43<em1Fzh>	involves: C57BL/6	N	28552195
MGI:6258953	M	MP:0002687	oligozoospermia	Cfap43<em2Fzh>/Cfap43<em2Fzh>	involves: C57BL/6	N	28552195
MGI:6258953	M	MP:0008545	absent sperm flagellum	Cfap43<em2Fzh>/Cfap43<em2Fzh>	involves: C57BL/6	N	28552195
MGI:6258953	M	MP:0001925	male infertility	Cfap43<em2Fzh>/Cfap43<em2Fzh>	involves: C57BL/6	N	28552195
MGI:6258953	M	MP:0009237	kinked sperm flagellum	Cfap43<em2Fzh>/Cfap43<em2Fzh>	involves: C57BL/6	N	28552195
MGI:6258953	M	MP:0031351	abnormal sperm flagellum thickness	Cfap43<em2Fzh>/Cfap43<em2Fzh>	involves: C57BL/6	N	28552195
MGI:6258953	M	MP:0031352	absent sperm axonemal central pair	Cfap43<em2Fzh>/Cfap43<em2Fzh>	involves: C57BL/6	N	28552195
MGI:6258953	M	MP:0009838	abnormal sperm axoneme morphology	Cfap43<em2Fzh>/Cfap43<em2Fzh>	involves: C57BL/6	N	28552195
MGI:6258953	M	MP:0031356	abnormal outer dense fiber morphology	Cfap43<em2Fzh>/Cfap43<em2Fzh>	involves: C57BL/6	N	28552195
MGI:6258953	M	MP:0002662	abnormal cauda epididymis morphology	Cfap43<em2Fzh>/Cfap43<em2Fzh>	involves: C57BL/6	N	28552195
MGI:6258953	M	MP:0009238	coiled sperm flagellum	Cfap43<em2Fzh>/Cfap43<em2Fzh>	involves: C57BL/6	N	28552195
MGI:6258953	M	MP:0008892	abnormal sperm flagellum morphology	Cfap43<em2Fzh>/Cfap43<em2Fzh>	involves: C57BL/6	N	28552195
MGI:6258953	M	MP:0002675	asthenozoospermia	Cfap43<em2Fzh>/Cfap43<em2Fzh>	involves: C57BL/6	N	28552195
MGI:6258953	M	MP:0009239	short sperm flagellum	Cfap43<em2Fzh>/Cfap43<em2Fzh>	involves: C57BL/6	N	28552195
MGI:6259146	M	MP:0001935	decreased litter size	Usp29<tm1Jkim>/Usp29<+>	involves: 129S7/SvEvBrd * C57BL/6J	N	27327533
MGI:6259148	F	MP:0008877	abnormal DNA methylation	Usp29<tm1Jkim>/Usp29<+>	involves: 129S7/SvEvBrd * C57BL/6J * PWD/PhJ	N	27327533
MGI:6259416	M	MP:0004255	abnormal spongiotrophoblast layer morphology	Ldoc1<tm1.1Tmki>/Ldoc1<tm1.1Tmki>	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259416	M	MP:0030989	decreased spongiotrophoblast cell number	Ldoc1<tm1.1Tmki>/Ldoc1<tm1.1Tmki>	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259416	M	MP:0005033	abnormal trophoblast giant cell morphology	Ldoc1<tm1.1Tmki>/Ldoc1<tm1.1Tmki>	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259416	M	MP:0001711	abnormal placenta morphology	Ldoc1<tm1.1Tmki>/Ldoc1<tm1.1Tmki>	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259416	M	MP:0005031	abnormal trophoblast layer morphology	Ldoc1<tm1.1Tmki>/Ldoc1<tm1.1Tmki>	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259417	F	MP:0001711	abnormal placenta morphology	Ldoc1<tm1.1Tmki>/Y	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259417	F	MP:0005033	abnormal trophoblast giant cell morphology	Ldoc1<tm1.1Tmki>/Y	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259417	F	MP:0030989	decreased spongiotrophoblast cell number	Ldoc1<tm1.1Tmki>/Y	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259417	F	MP:0005186	increased circulating progesterone level	Ldoc1<tm1.1Tmki>/Y	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259417	F	MP:0012008	delayed parturition	Ldoc1<tm1.1Tmki>/Y	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259417	F	MP:0011384	abnormal progesterone level	Ldoc1<tm1.1Tmki>/Y	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259417	F	MP:0001386	abnormal maternal nurturing	Ldoc1<tm1.1Tmki>/Y	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259417	F	MP:0004255	abnormal spongiotrophoblast layer morphology	Ldoc1<tm1.1Tmki>/Y	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259417	F	MP:0005031	abnormal trophoblast layer morphology	Ldoc1<tm1.1Tmki>/Y	B6.129S-Ldoc1<tm1.1Tmki>	N	25468940
MGI:6259526	M	MP:0000062	increased bone mineral density	Clcn7<tm1.1Mawa>/Clcn7<+>	involves: C57BL/6J * C57BL/6N * CD-1	N	28942122
MGI:6259526	M	MP:0004984	increased osteoclast cell number	Clcn7<tm1.1Mawa>/Clcn7<+>	involves: C57BL/6J * C57BL/6N * CD-1	N	28942122
MGI:6259526	M	MP:0004991	decreased bone strength	Clcn7<tm1.1Mawa>/Clcn7<+>	involves: C57BL/6J * C57BL/6N * CD-1	N	28942122
MGI:6259526	M	MP:0000135	decreased compact bone thickness	Clcn7<tm1.1Mawa>/Clcn7<+>	involves: C57BL/6J * C57BL/6N * CD-1	N	28942122
MGI:6259526	F	MP:0009347	increased trabecular bone thickness	Clcn7<tm1.1Mawa>/Clcn7<+>	involves: C57BL/6J * C57BL/6N * CD-1	N	28942122
MGI:6259526	M	MP:0010968	decreased compact bone area	Clcn7<tm1.1Mawa>/Clcn7<+>	involves: C57BL/6J * C57BL/6N * CD-1	N	28942122
MGI:6259537	F	MP:0001923	reduced female fertility	Tg(Mt1-Hgf)#Lmb/0	B6.FVB-Tg(Mt1-Hgf)#Lmb	N	16877364
MGI:6259614	F	MP:0004215	abnormal myocardial fiber physiology	Lamp2<tm1Psa>/Lamp2<tm1Psa>,Tg(CAG-RFP/EGFP/Map1lc3b)1Hill/0	involves: 129P2/OlaHsd * C57BL/6	N	28526246
MGI:6259615	F	MP:0004564	increased myocardial fiber size	Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd	N	28526246
MGI:6259615	F	MP:0004215	abnormal myocardial fiber physiology	Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd	N	28526246
MGI:6259615	F	MP:0006035	abnormal mitochondrial morphology	Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd	N	28526246
MGI:6259615	F	MP:0030940	impaired autophagy	Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd	N	28526246
MGI:6259615	F	MP:0021157	increased heart left ventricle wall thickness	Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd	N	28526246
MGI:6259615	F	MP:0014046	abnormal mitophagy	Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd	N	28526246
MGI:6259615	F	MP:0001544	abnormal cardiovascular system physiology	Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd	N	28526246
MGI:6259615	F	MP:0010954	abnormal cellular respiration	Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd	N	28526246
MGI:6259616	F	MP:0014046	abnormal mitophagy	Igs2<tm1(CAG-mt-Keima)Fink>/Igs2<+>,Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	N	28526246
MGI:6259616	F	MP:0004215	abnormal myocardial fiber physiology	Igs2<tm1(CAG-mt-Keima)Fink>/Igs2<+>,Lamp2<tm1Psa>/Lamp2<tm1Psa>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	N	28526246
MGI:6259651	M	MP:0001925	male infertility	Pmfbp1<em1Wli>/Pmfbp1<em1Wli>	involves: C57BL/6J * DBA/2J	N	30032984
MGI:6259651	M	MP:0009234	absent sperm head	Pmfbp1<em1Wli>/Pmfbp1<em1Wli>	involves: C57BL/6J * DBA/2J	N	30032984
MGI:6259651	M	MP:0009830	abnormal sperm connecting piece morphology	Pmfbp1<em1Wli>/Pmfbp1<em1Wli>	involves: C57BL/6J * DBA/2J	N	30032984
MGI:6259651	M	MP:0005389	reproductive system phenotype	Pmfbp1<em1Wli>/Pmfbp1<em1Wli>	involves: C57BL/6J * DBA/2J	Y	30032984
MGI:6259651	M	MP:0009838	abnormal sperm axoneme morphology	Pmfbp1<em1Wli>/Pmfbp1<em1Wli>	involves: C57BL/6J * DBA/2J	N	30032984
MGI:6259731	F	MP:0010767	abnormal female meiosis I arrest	Tut4<tm2.1Doca>/Tut4<tm2.1Doca>,Tut7<tm2.1Doca>/Tut7<tm2.1Doca>,Tg(Zp3-cre)93Knw/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	28792939
MGI:6259731	F	MP:0001926	female infertility	Tut4<tm2.1Doca>/Tut4<tm2.1Doca>,Tut7<tm2.1Doca>/Tut7<tm2.1Doca>,Tg(Zp3-cre)93Knw/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	28792939
MGI:6259731	F	MP:0000242	impaired fertilization	Tut4<tm2.1Doca>/Tut4<tm2.1Doca>,Tut7<tm2.1Doca>/Tut7<tm2.1Doca>,Tg(Zp3-cre)93Knw/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	28792939
MGI:6259731	F	MP:0014445	abnormal spindle assembly in female meiosis	Tut4<tm2.1Doca>/Tut4<tm2.1Doca>,Tut7<tm2.1Doca>/Tut7<tm2.1Doca>,Tg(Zp3-cre)93Knw/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	28792939
MGI:6259733	F	MP:0014445	abnormal spindle assembly in female meiosis	Tut4<tm2.1Doca>/Tut4<tm3.1Doca>,Tut7<tm2.1Doca>/Tut7<tm2.1Doca>,Tg(Zp3-cre)93Knw/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	28792939
MGI:6259733	F	MP:0001926	female infertility	Tut4<tm2.1Doca>/Tut4<tm3.1Doca>,Tut7<tm2.1Doca>/Tut7<tm2.1Doca>,Tg(Zp3-cre)93Knw/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	28792939
MGI:6259733	F	MP:0010767	abnormal female meiosis I arrest	Tut4<tm2.1Doca>/Tut4<tm3.1Doca>,Tut7<tm2.1Doca>/Tut7<tm2.1Doca>,Tg(Zp3-cre)93Knw/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	28792939
MGI:6259733	F	MP:0000242	impaired fertilization	Tut4<tm2.1Doca>/Tut4<tm3.1Doca>,Tut7<tm2.1Doca>/Tut7<tm2.1Doca>,Tg(Zp3-cre)93Knw/0	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	N	28792939
MGI:6259805	F	MP:0001325	abnormal retina morphology	Opn1mw<tm1a(EUCOMM)Wtsi>/Opn1mw<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	28751656
MGI:6259805	F	MP:0012144	decreased b-wave amplitude	Opn1mw<tm1a(EUCOMM)Wtsi>/Opn1mw<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	28751656
MGI:6261736	M	MP:0001488	increased startle reflex	0610010K14Rik<tm1.1(KOMP)Vlcg>/0610010K14Rik<+>	C57BL/6N-0610010K14Rik<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6261739	F	MP:0005562	decreased mean corpuscular hemoglobin	Ecrg4<tm1b(EUCOMM)Hmgu>/Ecrg4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ecrg4<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6261739	M	MP:0005178	increased circulating cholesterol level	Ecrg4<tm1b(EUCOMM)Hmgu>/Ecrg4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ecrg4<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6261739	M	MP:0002764	short tibia	Ecrg4<tm1b(EUCOMM)Hmgu>/Ecrg4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ecrg4<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6261739	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Ecrg4<tm1b(EUCOMM)Hmgu>/Ecrg4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ecrg4<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6261739	F	MP:0001257	increased body length	Ecrg4<tm1b(EUCOMM)Hmgu>/Ecrg4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ecrg4<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6261741	F	MP:0011239	abnormal skin coloration	1700012B09Rik<tm1.1(KOMP)Wtsi>/1700012B09Rik<tm1.1(KOMP)Wtsi>	C57BL/6N-1700012B09Rik<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6261742	M	MP:0001925	male infertility	Frey1<tm1.1(KOMP)Vlcg>/Frey1<tm1.1(KOMP)Vlcg>	C57BL/6N-Frey1<tm1.1(KOMP)Vlcg>/Mmucd	N	MGI:5576271
MGI:6261742	M	MP:0005554	decreased circulating creatinine level	Frey1<tm1.1(KOMP)Vlcg>/Frey1<tm1.1(KOMP)Vlcg>	C57BL/6N-Frey1<tm1.1(KOMP)Vlcg>/Mmucd	N	MGI:5576271
MGI:6261742	F	MP:0002060	abnormal skin morphology	Frey1<tm1.1(KOMP)Vlcg>/Frey1<tm1.1(KOMP)Vlcg>	C57BL/6N-Frey1<tm1.1(KOMP)Vlcg>/Mmucd	N	MGI:5576271
MGI:6261742	M	MP:0000198	decreased circulating phosphate level	Frey1<tm1.1(KOMP)Vlcg>/Frey1<tm1.1(KOMP)Vlcg>	C57BL/6N-Frey1<tm1.1(KOMP)Vlcg>/Mmucd	N	MGI:5576271
MGI:6261746	M	MP:0003961	decreased lean body mass	2210408I21Rik<tm1b(EUCOMM)Wtsi>/2210408I21Rik<tm1b(EUCOMM)Wtsi>	C57BL/6N-2210408I21Rik<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261746	F	MP:0001102	small superior vagus ganglion	2210408I21Rik<tm1b(EUCOMM)Wtsi>/2210408I21Rik<tm1b(EUCOMM)Wtsi>	C57BL/6N-2210408I21Rik<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261746	F	MP:0002135	abnormal kidney morphology	2210408I21Rik<tm1b(EUCOMM)Wtsi>/2210408I21Rik<tm1b(EUCOMM)Wtsi>	C57BL/6N-2210408I21Rik<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261746	F	MP:0010124	decreased bone mineral content	2210408I21Rik<tm1b(EUCOMM)Wtsi>/2210408I21Rik<tm1b(EUCOMM)Wtsi>	C57BL/6N-2210408I21Rik<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261746	F	MP:0009709	hydrometra	2210408I21Rik<tm1b(EUCOMM)Wtsi>/2210408I21Rik<tm1b(EUCOMM)Wtsi>	C57BL/6N-2210408I21Rik<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261746	F	MP:0005293	impaired glucose tolerance	2210408I21Rik<tm1b(EUCOMM)Wtsi>/2210408I21Rik<tm1b(EUCOMM)Wtsi>	C57BL/6N-2210408I21Rik<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261747	M	MP:0005554	decreased circulating creatinine level	Micos13<tm1.1(KOMP)Vlcg>/Micos13<+>	C57BL/6N-Micos13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261747	M	MP:0005566	decreased blood urea nitrogen level	Micos13<tm1.1(KOMP)Vlcg>/Micos13<+>	C57BL/6N-Micos13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261747	M	MP:0000198	decreased circulating phosphate level	Micos13<tm1.1(KOMP)Vlcg>/Micos13<+>	C57BL/6N-Micos13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261747	M	MP:0005179	decreased circulating cholesterol level	Micos13<tm1.1(KOMP)Vlcg>/Micos13<+>	C57BL/6N-Micos13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261747	M	MP:0000186	decreased circulating HDL cholesterol level	Micos13<tm1.1(KOMP)Vlcg>/Micos13<+>	C57BL/6N-Micos13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261748	F	MP:0009709	hydrometra	2700054A10Rik<em2(IMPC)Mbp>/2700054A10Rik<em2(IMPC)Mbp>	C57BL/6NCrl-2700054A10Rik<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261748	M	MP:0001402	decreased locomotor activity	2700054A10Rik<em2(IMPC)Mbp>/2700054A10Rik<em2(IMPC)Mbp>	C57BL/6NCrl-2700054A10Rik<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261748	F	MP:0001566	increased circulating phosphate level	2700054A10Rik<em2(IMPC)Mbp>/2700054A10Rik<em2(IMPC)Mbp>	C57BL/6NCrl-2700054A10Rik<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261748	F	MP:0001293	anophthalmia	2700054A10Rik<em2(IMPC)Mbp>/2700054A10Rik<em2(IMPC)Mbp>	C57BL/6NCrl-2700054A10Rik<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261748	F	MP:0002092	abnormal eye morphology	2700054A10Rik<em2(IMPC)Mbp>/2700054A10Rik<em2(IMPC)Mbp>	C57BL/6NCrl-2700054A10Rik<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261748	F	MP:0001102	small superior vagus ganglion	2700054A10Rik<em2(IMPC)Mbp>/2700054A10Rik<em2(IMPC)Mbp>	C57BL/6NCrl-2700054A10Rik<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261749	M	MP:0010067	increased red blood cell distribution width	Cep15<tm1b(KOMP)Wtsi>/Cep15<tm1b(KOMP)Wtsi>	C57BL/6N-Cep15<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261750	F	MP:0001926	female infertility	4930451I11Rik<tm1.1(KOMP)Wtsi>/4930451I11Rik<tm1.1(KOMP)Wtsi>	C57BL/6N-4930451I11Rik<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6261750	M	MP:0001925	male infertility	4930451I11Rik<tm1.1(KOMP)Wtsi>/4930451I11Rik<tm1.1(KOMP)Wtsi>	C57BL/6N-4930451I11Rik<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6261751	M	MP:0013278	decreased fasting circulating glucose level	4930563E22Rik<tm1.1(KOMP)Vlcg>/4930563E22Rik<tm1.1(KOMP)Vlcg>	B6N(Cg)-4930563E22Rik<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6261752	M	MP:0001925	male infertility	4930590J08Rik<tm1a(EUCOMM)Wtsi>/4930590J08Rik<tm1a(EUCOMM)Wtsi>	C57BL/6N-4930590J08Rik<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261754	F	MP:0001257	increased body length	4931422A03Rik<tm1b(EUCOMM)Wtsi>/4931422A03Rik<tm1b(EUCOMM)Wtsi>	C57BL/6N-4931422A03Rik<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6261755	M	MP:0005565	increased blood urea nitrogen level	4931429L15Rik<tm1a(EUCOMM)Wtsi>/4931429L15Rik<tm1a(EUCOMM)Wtsi>	C57BL/6N-4931429L15Rik<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261755	F	MP:0000195	decreased circulating calcium level	4931429L15Rik<tm1a(EUCOMM)Wtsi>/4931429L15Rik<tm1a(EUCOMM)Wtsi>	C57BL/6N-4931429L15Rik<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261759	F	MP:0002111	abnormal tail morphology	Cdcp3<em1(IMPC)Mbp>/Cdcp3<em1(IMPC)Mbp>	C57BL/6NCrl-Cdcp3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261759	F	MP:0002092	abnormal eye morphology	Cdcp3<em1(IMPC)Mbp>/Cdcp3<em1(IMPC)Mbp>	C57BL/6NCrl-Cdcp3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261761	F	MP:0002060	abnormal skin morphology	Cstdc2<em1(IMPC)Tcp>/Cstdc2<em1(IMPC)Tcp>	C57BL/6NCrl-Cstdc2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261761	F	MP:0003020	decreased circulating chloride level	Cstdc2<em1(IMPC)Tcp>/Cstdc2<em1(IMPC)Tcp>	C57BL/6NCrl-Cstdc2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261764	M	MP:0005344	increased circulating bilirubin level	Shfl<tm1.1(KOMP)Mbp>/Shfl<tm1.1(KOMP)Mbp>	C57BL/6N-Shfl<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6261764	M	MP:0000494	abnormal cecum morphology	Shfl<tm1.1(KOMP)Mbp>/Shfl<tm1.1(KOMP)Mbp>	C57BL/6N-Shfl<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6261764	M	MP:0004931	enlarged epididymis	Shfl<tm1.1(KOMP)Mbp>/Shfl<tm1.1(KOMP)Mbp>	C57BL/6N-Shfl<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6261766	F	MP:0010053	decreased grip strength	Aasdhppt<tm1.1(KOMP)Vlcg>/Aasdhppt<+>	B6N(Cg)-Aasdhppt<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6261768	F	MP:0000157	abnormal sternum morphology	Aass<em1(IMPC)Tcp>/Aass<em1(IMPC)Tcp>	C57BL/6NCrl-Aass<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261768	M	MP:0011874	enlarged urinary bladder	Aass<em1(IMPC)Tcp>/Aass<em1(IMPC)Tcp>	C57BL/6NCrl-Aass<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261768	M	MP:0000702	enlarged lymph nodes	Aass<em1(IMPC)Tcp>/Aass<em1(IMPC)Tcp>	C57BL/6NCrl-Aass<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261769	F	MP:0002968	increased circulating alkaline phosphatase level	Abca17<tm1b(EUCOMM)Wtsi>/Abca17<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abca17<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6261769	F	MP:0005628	decreased circulating potassium level	Abca17<tm1b(EUCOMM)Wtsi>/Abca17<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abca17<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6261772	M	MP:0020870	decreased thigmotaxis	Abca9<em1(IMPC)J>/Abca9<em1(IMPC)J>	C57BL/6NJ-Abca9<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261773	M	MP:0000195	decreased circulating calcium level	Abcc5<em1(IMPC)H>/Abcc5<em1(IMPC)H>	C57BL/6N-Abcc5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261773	F	MP:0001513	limb grasping	Abcc5<em1(IMPC)H>/Abcc5<em1(IMPC)H>	C57BL/6N-Abcc5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261773	M	MP:0000221	decreased leukocyte cell number	Abcc5<em1(IMPC)H>/Abcc5<em1(IMPC)H>	C57BL/6N-Abcc5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261773	M	MP:0005565	increased blood urea nitrogen level	Abcc5<em1(IMPC)H>/Abcc5<em1(IMPC)H>	C57BL/6N-Abcc5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261773	F	MP:0005293	impaired glucose tolerance	Abcc5<em1(IMPC)H>/Abcc5<em1(IMPC)H>	C57BL/6N-Abcc5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261773	M	MP:0005012	decreased eosinophil cell number	Abcc5<em1(IMPC)H>/Abcc5<em1(IMPC)H>	C57BL/6N-Abcc5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261773	F	MP:0001488	increased startle reflex	Abcc5<em1(IMPC)H>/Abcc5<em1(IMPC)H>	C57BL/6N-Abcc5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261773	M	MP:0005016	decreased lymphocyte cell number	Abcc5<em1(IMPC)H>/Abcc5<em1(IMPC)H>	C57BL/6N-Abcc5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261774	M	MP:0010052	increased grip strength	Abcd3<em1(IMPC)J>/Abcd3<em1(IMPC)J>	C57BL/6NJ-Abcd3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261774	F	MP:0005278	abnormal cholesterol homeostasis	Abcd3<em1(IMPC)J>/Abcd3<em1(IMPC)J>	C57BL/6NJ-Abcd3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261774	F	MP:0005568	increased circulating total protein level	Abcd3<em1(IMPC)J>/Abcd3<em1(IMPC)J>	C57BL/6NJ-Abcd3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261774	M	MP:0005292	improved glucose tolerance	Abcd3<em1(IMPC)J>/Abcd3<em1(IMPC)J>	C57BL/6NJ-Abcd3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261774	M	MP:0010025	decreased total body fat amount	Abcd3<em1(IMPC)J>/Abcd3<em1(IMPC)J>	C57BL/6NJ-Abcd3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261774	F	MP:0000194	increased circulating calcium level	Abcd3<em1(IMPC)J>/Abcd3<em1(IMPC)J>	C57BL/6NJ-Abcd3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261774	M	MP:0000063	decreased bone mineral density	Abcd3<em1(IMPC)J>/Abcd3<em1(IMPC)J>	C57BL/6NJ-Abcd3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261775	M	MP:0002059	abnormal seminal vesicle morphology	Abce1<tm1.1(KOMP)Vlcg>/Abce1<+>	C57BL/6N-Abce1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6261775	M	MP:0000702	enlarged lymph nodes	Abce1<tm1.1(KOMP)Vlcg>/Abce1<+>	C57BL/6N-Abce1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6261775	M	MP:0000219	increased neutrophil cell number	Abce1<tm1.1(KOMP)Vlcg>/Abce1<+>	C57BL/6N-Abce1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6261777	M	MP:0012362	increased large unstained cell number	Abce1<tm1b(EUCOMM)Hmgu>/Abce1<+>	C57BL/6N-Abce1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6261777	F	MP:0005554	decreased circulating creatinine level	Abce1<tm1b(EUCOMM)Hmgu>/Abce1<+>	C57BL/6N-Abce1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6261779	M	MP:0001925	male infertility	Abhd10<em1(IMPC)Mbp>/Abhd10<em1(IMPC)Mbp>	C57BL/6NCrl-Abhd10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261779	M	MP:0002606	increased basophil cell number	Abhd10<em1(IMPC)Mbp>/Abhd10<em1(IMPC)Mbp>	C57BL/6NCrl-Abhd10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261780	F	MP:0009709	hydrometra	Abhd11<em1(IMPC)Mbp>/Abhd11<em1(IMPC)Mbp>	C57BL/6N-Abhd11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261780	M	MP:0000538	abnormal urinary bladder morphology	Abhd11<em1(IMPC)Mbp>/Abhd11<em1(IMPC)Mbp>	C57BL/6N-Abhd11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261780	F	MP:0001102	small superior vagus ganglion	Abhd11<em1(IMPC)Mbp>/Abhd11<em1(IMPC)Mbp>	C57BL/6N-Abhd11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261781	M	MP:0013278	decreased fasting circulating glucose level	Abhd16a<tm1a(EUCOMM)Wtsi>/Abhd16a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Abhd16a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261781	M	MP:0001925	male infertility	Abhd16a<tm1a(EUCOMM)Wtsi>/Abhd16a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Abhd16a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261781	M	MP:0010093	decreased circulating magnesium level	Abhd16a<tm1a(EUCOMM)Wtsi>/Abhd16a<tm1a(EUCOMM)Wtsi>	C57BL/6N-Abhd16a<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261782	F	MP:0009252	absent urinary bladder	Abi2<tm1b(EUCOMM)Wtsi>/Abi2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abi2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261782	M	MP:0002059	abnormal seminal vesicle morphology	Abi2<tm1b(EUCOMM)Wtsi>/Abi2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abi2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261782	M	MP:0002941	increased circulating alanine transaminase level	Abi2<tm1b(EUCOMM)Wtsi>/Abi2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abi2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261782	M	MP:0001147	small testis	Abi2<tm1b(EUCOMM)Wtsi>/Abi2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abi2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261782	M	MP:0013279	increased fasting circulating glucose level	Abi2<tm1b(EUCOMM)Wtsi>/Abi2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abi2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261783	F	MP:0010052	increased grip strength	Acadm<tm1b(EUCOMM)Hmgu>/Acadm<tm1b(EUCOMM)Hmgu>	C57BL/6N-Acadm<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6261783	M	MP:0002098	abnormal vibrissa morphology	Acadm<tm1b(EUCOMM)Hmgu>/Acadm<tm1b(EUCOMM)Hmgu>	C57BL/6N-Acadm<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6261783	M	MP:0002764	short tibia	Acadm<tm1b(EUCOMM)Hmgu>/Acadm<tm1b(EUCOMM)Hmgu>	C57BL/6N-Acadm<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6261784	M	MP:0000452	abnormal mouth morphology	Acadsb<em1(IMPC)J>/Acadsb<em1(IMPC)J>	C57BL/6NJ-Acadsb<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261784	M	MP:0020870	decreased thigmotaxis	Acadsb<em1(IMPC)J>/Acadsb<em1(IMPC)J>	C57BL/6NJ-Acadsb<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261784	F	MP:0004222	iris synechia	Acadsb<em1(IMPC)J>/Acadsb<em1(IMPC)J>	C57BL/6NJ-Acadsb<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261784	M	MP:0002098	abnormal vibrissa morphology	Acadsb<em1(IMPC)J>/Acadsb<em1(IMPC)J>	C57BL/6NJ-Acadsb<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261785	M	MP:0001556	increased circulating HDL cholesterol level	Acan<tm1b(EUCOMM)Hmgu>/Acan<+>	C57BL/6N-Acan<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6261788	M	MP:0002599	increased mean platelet volume	Acmsd<tm1b(EUCOMM)Hmgu>/Acmsd<tm1b(EUCOMM)Hmgu>	C57BL/6N-Acmsd<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261788	M	MP:0000062	increased bone mineral density	Acmsd<tm1b(EUCOMM)Hmgu>/Acmsd<tm1b(EUCOMM)Hmgu>	C57BL/6N-Acmsd<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261790	M	MP:0002591	decreased mean corpuscular volume	Acot2<em1(IMPC)J>/Acot2<em1(IMPC)J>	C57BL/6NJ-Acot2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261791	M	MP:0005553	increased circulating creatinine level	Actg2<em1(IMPC)J>/Actg2<em1(IMPC)J>	C57BL/6NJ-Actg2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261791	F	MP:0002098	abnormal vibrissa morphology	Actg2<em1(IMPC)J>/Actg2<em1(IMPC)J>	C57BL/6NJ-Actg2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261792	M	MP:0000274	enlarged heart	Actl7b<tm1.1(KOMP)Vlcg>/Actl7b<tm1.1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6261792	M	MP:0000266	abnormal heart morphology	Actl7b<tm1.1(KOMP)Vlcg>/Actl7b<tm1.1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6261792	M	MP:0001925	male infertility	Actl7b<tm1.1(KOMP)Vlcg>/Actl7b<tm1.1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6261792	M	MP:0000538	abnormal urinary bladder morphology	Actl7b<tm1.1(KOMP)Vlcg>/Actl7b<tm1.1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6261794	M	MP:0003179	thrombocytopenia	Adal<tm1a(EUCOMM)Wtsi>/Adal<tm1a(EUCOMM)Wtsi>	C57BL/6N-Adal<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261796	M	MP:0001146	abnormal testis morphology	Adam26a<tm1.1(KOMP)Vlcg>/Adam26a<tm1.1(KOMP)Vlcg>	C57BL/6N-Adam26a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261796	M	MP:0004931	enlarged epididymis	Adam26a<tm1.1(KOMP)Vlcg>/Adam26a<tm1.1(KOMP)Vlcg>	C57BL/6N-Adam26a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261796	M	MP:0001147	small testis	Adam26a<tm1.1(KOMP)Vlcg>/Adam26a<tm1.1(KOMP)Vlcg>	C57BL/6N-Adam26a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261796	M	MP:0002631	abnormal epididymis morphology	Adam26a<tm1.1(KOMP)Vlcg>/Adam26a<tm1.1(KOMP)Vlcg>	C57BL/6N-Adam26a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261797	M	MP:0010124	decreased bone mineral content	Adam32<tm1b(KOMP)Wtsi>/Adam32<tm1b(KOMP)Wtsi>	B6N(Cg)-Adam32<tm1b(KOMP)Wtsi>/2J	N	MGI:5576271
MGI:6261797	M	MP:0000063	decreased bone mineral density	Adam32<tm1b(KOMP)Wtsi>/Adam32<tm1b(KOMP)Wtsi>	B6N(Cg)-Adam32<tm1b(KOMP)Wtsi>/2J	N	MGI:5576271
MGI:6261797	M	MP:0006243	impaired pupillary reflex	Adam32<tm1b(KOMP)Wtsi>/Adam32<tm1b(KOMP)Wtsi>	B6N(Cg)-Adam32<tm1b(KOMP)Wtsi>/2J	N	MGI:5576271
MGI:6261797	M	MP:0010024	increased total body fat amount	Adam32<tm1b(KOMP)Wtsi>/Adam32<tm1b(KOMP)Wtsi>	B6N(Cg)-Adam32<tm1b(KOMP)Wtsi>/2J	N	MGI:5576271
MGI:6261797	M	MP:0003961	decreased lean body mass	Adam32<tm1b(KOMP)Wtsi>/Adam32<tm1b(KOMP)Wtsi>	B6N(Cg)-Adam32<tm1b(KOMP)Wtsi>/2J	N	MGI:5576271
MGI:6261798	M	MP:0000274	enlarged heart	Adam8<tm1.1(KOMP)Vlcg>/Adam8<tm1.1(KOMP)Vlcg>	C57BL/6N-Adam8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261798	M	MP:0000266	abnormal heart morphology	Adam8<tm1.1(KOMP)Vlcg>/Adam8<tm1.1(KOMP)Vlcg>	C57BL/6N-Adam8<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261799	F	MP:0001304	cataract	Adamts14<em1(IMPC)J>/Adamts14<em1(IMPC)J>	C57BL/6NJ-Adamts14<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261800	M	MP:0001925	male infertility	Adamts15<tm1.1(KOMP)Vlcg>/Adamts15<tm1.1(KOMP)Vlcg>	C57BL/6N-Adamts15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261800	M	MP:0002079	increased circulating insulin level	Adamts15<tm1.1(KOMP)Vlcg>/Adamts15<tm1.1(KOMP)Vlcg>	C57BL/6N-Adamts15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261800	M	MP:0004931	enlarged epididymis	Adamts15<tm1.1(KOMP)Vlcg>/Adamts15<tm1.1(KOMP)Vlcg>	C57BL/6N-Adamts15<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261801	M	MP:0001556	increased circulating HDL cholesterol level	Adamts16<em1(IMPC)H>/Adamts16<em1(IMPC)H>	C57BL/6N-Adamts16<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261801	M	MP:0010024	increased total body fat amount	Adamts16<em1(IMPC)H>/Adamts16<em1(IMPC)H>	C57BL/6N-Adamts16<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261801	M	MP:0010124	decreased bone mineral content	Adamts16<em1(IMPC)H>/Adamts16<em1(IMPC)H>	C57BL/6N-Adamts16<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261801	M	MP:0000745	tremors	Adamts16<em1(IMPC)H>/Adamts16<em1(IMPC)H>	C57BL/6N-Adamts16<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261802	F	MP:0000702	enlarged lymph nodes	Adamtsl3<em1(IMPC)Tcp>/Adamtsl3<em1(IMPC)Tcp>	C57BL/6NCrl-Adamtsl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261802	M	MP:0000157	abnormal sternum morphology	Adamtsl3<em1(IMPC)Tcp>/Adamtsl3<em1(IMPC)Tcp>	C57BL/6NCrl-Adamtsl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261802	M	MP:0011874	enlarged urinary bladder	Adamtsl3<em1(IMPC)Tcp>/Adamtsl3<em1(IMPC)Tcp>	C57BL/6NCrl-Adamtsl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261802	F	MP:0002637	small uterus	Adamtsl3<em1(IMPC)Tcp>/Adamtsl3<em1(IMPC)Tcp>	C57BL/6NCrl-Adamtsl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261802	M	MP:0000692	small spleen	Adamtsl3<em1(IMPC)Tcp>/Adamtsl3<em1(IMPC)Tcp>	C57BL/6NCrl-Adamtsl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261802	M	MP:0000274	enlarged heart	Adamtsl3<em1(IMPC)Tcp>/Adamtsl3<em1(IMPC)Tcp>	C57BL/6NCrl-Adamtsl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261802	F	MP:0001126	abnormal ovary morphology	Adamtsl3<em1(IMPC)Tcp>/Adamtsl3<em1(IMPC)Tcp>	C57BL/6NCrl-Adamtsl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261803	F	MP:0001289	persistence of hyaloid vascular system	Adamtsl4<em1(IMPC)J>/Adamtsl4<em1(IMPC)J>	C57BL/6NJ-Adamtsl4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261803	F	MP:0001319	irregularly shaped pupil	Adamtsl4<em1(IMPC)J>/Adamtsl4<em1(IMPC)J>	C57BL/6NJ-Adamtsl4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261803	M	MP:0003131	increased erythrocyte cell number	Adamtsl4<em1(IMPC)J>/Adamtsl4<em1(IMPC)J>	C57BL/6NJ-Adamtsl4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261803	F	MP:0002098	abnormal vibrissa morphology	Adamtsl4<em1(IMPC)J>/Adamtsl4<em1(IMPC)J>	C57BL/6NJ-Adamtsl4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261803	F	MP:0006241	abnormal placement of pupils	Adamtsl4<em1(IMPC)J>/Adamtsl4<em1(IMPC)J>	C57BL/6NJ-Adamtsl4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261803	F	MP:0000367	abnormal coat/ hair morphology	Adamtsl4<em1(IMPC)J>/Adamtsl4<em1(IMPC)J>	C57BL/6NJ-Adamtsl4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261803	F	MP:0010052	increased grip strength	Adamtsl4<em1(IMPC)J>/Adamtsl4<em1(IMPC)J>	C57BL/6NJ-Adamtsl4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261803	F	MP:0010053	decreased grip strength	Adamtsl4<em1(IMPC)J>/Adamtsl4<em1(IMPC)J>	C57BL/6NJ-Adamtsl4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261803	F	MP:0001284	absent vibrissae	Adamtsl4<em1(IMPC)J>/Adamtsl4<em1(IMPC)J>	C57BL/6NJ-Adamtsl4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261805	M	MP:0000689	abnormal spleen morphology	Adarb2<em1(IMPC)Tcp>/Adarb2<em1(IMPC)Tcp>	C57BL/6NCrl-Adarb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261805	M	MP:0001147	small testis	Adarb2<em1(IMPC)Tcp>/Adarb2<em1(IMPC)Tcp>	C57BL/6NCrl-Adarb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261805	F	MP:0000367	abnormal coat/ hair morphology	Adarb2<em1(IMPC)Tcp>/Adarb2<em1(IMPC)Tcp>	C57BL/6NCrl-Adarb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261805	F	MP:0001513	limb grasping	Adarb2<em1(IMPC)Tcp>/Adarb2<em1(IMPC)Tcp>	C57BL/6NCrl-Adarb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261805	M	MP:0002989	small kidney	Adarb2<em1(IMPC)Tcp>/Adarb2<em1(IMPC)Tcp>	C57BL/6NCrl-Adarb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261807	M	MP:0000702	enlarged lymph nodes	Adck1<em2(IMPC)Tcp>/Adck1<em2(IMPC)Tcp>	C57BL/6NCrl-Adck1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261808	M	MP:0000218	increased leukocyte cell number	Adcy1<tm1b(EUCOMM)Wtsi>/Adcy1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Adcy1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6261808	F	MP:0001392	abnormal locomotor behavior	Adcy1<tm1b(EUCOMM)Wtsi>/Adcy1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Adcy1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6261808	M	MP:0002590	increased mean corpuscular volume	Adcy1<tm1b(EUCOMM)Wtsi>/Adcy1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Adcy1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6261808	M	MP:0001406	abnormal gait	Adcy1<tm1b(EUCOMM)Wtsi>/Adcy1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Adcy1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6261808	M	MP:0001566	increased circulating phosphate level	Adcy1<tm1b(EUCOMM)Wtsi>/Adcy1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Adcy1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6261808	F	MP:0001415	increased exploration in new environment	Adcy1<tm1b(EUCOMM)Wtsi>/Adcy1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Adcy1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6261809	F	MP:0005564	increased hemoglobin content	Adcy3<tm1a(EUCOMM)Wtsi>/Adcy3<+>	C57BL/6N-Adcy3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261809	F	MP:0010024	increased total body fat amount	Adcy3<tm1a(EUCOMM)Wtsi>/Adcy3<+>	C57BL/6N-Adcy3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261809	F	MP:0003961	decreased lean body mass	Adcy3<tm1a(EUCOMM)Wtsi>/Adcy3<+>	C57BL/6N-Adcy3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261809	F	MP:0002608	increased hematocrit	Adcy3<tm1a(EUCOMM)Wtsi>/Adcy3<+>	C57BL/6N-Adcy3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261811	F	MP:0001120	abnormal uterus morphology	Adgb<em1(IMPC)Mbp>/Adgb<+>	C57BL/6NCrl-Adgb<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261811	F	MP:0002135	abnormal kidney morphology	Adgb<em1(IMPC)Mbp>/Adgb<+>	C57BL/6NCrl-Adgb<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261811	F	MP:0009709	hydrometra	Adgb<em1(IMPC)Mbp>/Adgb<+>	C57BL/6NCrl-Adgb<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261811	M	MP:0020421	increased freezing behavior	Adgb<em1(IMPC)Mbp>/Adgb<+>	C57BL/6NCrl-Adgb<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261811	F	MP:0005011	increased eosinophil cell number	Adgb<em1(IMPC)Mbp>/Adgb<+>	C57BL/6NCrl-Adgb<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261811	F	MP:0002092	abnormal eye morphology	Adgb<em1(IMPC)Mbp>/Adgb<+>	C57BL/6NCrl-Adgb<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261812	F	MP:0001891	hydrocephaly	Adgb<em1(IMPC)Mbp>/Adgb<em1(IMPC)Mbp>	C57BL/6NCrl-Adgb<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261812	M	MP:0001925	male infertility	Adgb<em1(IMPC)Mbp>/Adgb<em1(IMPC)Mbp>	C57BL/6NCrl-Adgb<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261812	M	MP:0004818	increased skeletal muscle mass	Adgb<em1(IMPC)Mbp>/Adgb<em1(IMPC)Mbp>	C57BL/6NCrl-Adgb<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261812	F	MP:0002152	abnormal brain morphology	Adgb<em1(IMPC)Mbp>/Adgb<em1(IMPC)Mbp>	C57BL/6NCrl-Adgb<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261813	M	MP:0010123	increased bone mineral content	Adgra1<tm1b(EUCOMM)Hmgu>/Adgra1<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Adgra1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6261813	F	MP:0005292	improved glucose tolerance	Adgra1<tm1b(EUCOMM)Hmgu>/Adgra1<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Adgra1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6261814	M	MP:0000274	enlarged heart	Adipoq<tm1b(KOMP)Wtsi>/Adipoq<tm1b(KOMP)Wtsi>	C57BL/6N-Adipoq<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6261814	M	MP:0000266	abnormal heart morphology	Adipoq<tm1b(KOMP)Wtsi>/Adipoq<tm1b(KOMP)Wtsi>	C57BL/6N-Adipoq<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6261815	M	MP:0000195	decreased circulating calcium level	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6261815	F	MP:0003731	abnormal retina outer nuclear layer morphology	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6261815	F	MP:0001566	increased circulating phosphate level	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6261815	F	MP:0002966	decreased circulating alkaline phosphatase level	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6261815	F	MP:0001552	increased circulating triglyceride level	Adipor1<tm1b(EUCOMM)Hmgu>/Adipor1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adipor1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6261816	M	MP:0001147	small testis	Adm2<tm1.1(KOMP)Vlcg>/Adm2<tm1.1(KOMP)Vlcg>	C57BL/6N-Adm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261816	F	MP:0001126	abnormal ovary morphology	Adm2<tm1.1(KOMP)Vlcg>/Adm2<tm1.1(KOMP)Vlcg>	C57BL/6N-Adm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261816	M	MP:0001146	abnormal testis morphology	Adm2<tm1.1(KOMP)Vlcg>/Adm2<tm1.1(KOMP)Vlcg>	C57BL/6N-Adm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261816	F	MP:0008725	increased heart atrium size	Adm2<tm1.1(KOMP)Vlcg>/Adm2<tm1.1(KOMP)Vlcg>	C57BL/6N-Adm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261816	F	MP:0000266	abnormal heart morphology	Adm2<tm1.1(KOMP)Vlcg>/Adm2<tm1.1(KOMP)Vlcg>	C57BL/6N-Adm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261817	F	MP:0003795	abnormal bone structure	Adnp2<em3(IMPC)Tcp>/Adnp2<em3(IMPC)Tcp>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261817	F	MP:0001175	abnormal lung morphology	Adnp2<em3(IMPC)Tcp>/Adnp2<em3(IMPC)Tcp>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261817	F	MP:0001120	abnormal uterus morphology	Adnp2<em3(IMPC)Tcp>/Adnp2<em3(IMPC)Tcp>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261817	F	MP:0000063	decreased bone mineral density	Adnp2<em3(IMPC)Tcp>/Adnp2<em3(IMPC)Tcp>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261817	F	MP:0001399	hyperactivity	Adnp2<em3(IMPC)Tcp>/Adnp2<em3(IMPC)Tcp>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261817	F	MP:0000598	abnormal liver morphology	Adnp2<em3(IMPC)Tcp>/Adnp2<em3(IMPC)Tcp>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261817	M	MP:0010052	increased grip strength	Adnp2<em3(IMPC)Tcp>/Adnp2<em3(IMPC)Tcp>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261817	F	MP:0010124	decreased bone mineral content	Adnp2<em3(IMPC)Tcp>/Adnp2<em3(IMPC)Tcp>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261817	F	MP:0005567	decreased circulating total protein level	Adnp2<em3(IMPC)Tcp>/Adnp2<em3(IMPC)Tcp>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261817	F	MP:0005419	decreased circulating serum albumin level	Adnp2<em3(IMPC)Tcp>/Adnp2<em3(IMPC)Tcp>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261818	F	MP:0002574	increased vertical activity	Adora1<tm1b(KOMP)Wtsi>/Adora1<tm1b(KOMP)Wtsi>	B6N(Cg)-Adora1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6261818	F	MP:0001415	increased exploration in new environment	Adora1<tm1b(KOMP)Wtsi>/Adora1<tm1b(KOMP)Wtsi>	B6N(Cg)-Adora1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6261819	M	MP:0010025	decreased total body fat amount	Adprs<em1(IMPC)Wtsi>/Adprs<em1(IMPC)Wtsi>	C57BL/6N-Adprs<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6261819	M	MP:0010123	increased bone mineral content	Adprs<em1(IMPC)Wtsi>/Adprs<em1(IMPC)Wtsi>	C57BL/6N-Adprs<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6261819	M	MP:0003960	increased lean body mass	Adprs<em1(IMPC)Wtsi>/Adprs<em1(IMPC)Wtsi>	C57BL/6N-Adprs<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6261819	M	MP:0000062	increased bone mineral density	Adprs<em1(IMPC)Wtsi>/Adprs<em1(IMPC)Wtsi>	C57BL/6N-Adprs<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6261819	F	MP:0002968	increased circulating alkaline phosphatase level	Adprs<em1(IMPC)Wtsi>/Adprs<em1(IMPC)Wtsi>	C57BL/6N-Adprs<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6261820	F	MP:0001402	decreased locomotor activity	Adprm<tm1b(EUCOMM)Hmgu>/Adprm<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adprm<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261820	F	MP:0001399	hyperactivity	Adprm<tm1b(EUCOMM)Hmgu>/Adprm<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adprm<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261820	M	MP:0001489	decreased startle reflex	Adprm<tm1b(EUCOMM)Hmgu>/Adprm<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adprm<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261820	F	MP:0010379	decreased respiratory quotient	Adprm<tm1b(EUCOMM)Hmgu>/Adprm<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adprm<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261821	F	MP:0001556	increased circulating HDL cholesterol level	Adss2<tm1b(EUCOMM)Wtsi>/Adss2<+>	C57BL/6N-Adss2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6261821	F	MP:0005554	decreased circulating creatinine level	Adss2<tm1b(EUCOMM)Wtsi>/Adss2<+>	C57BL/6N-Adss2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6261821	F	MP:0005566	decreased blood urea nitrogen level	Adss2<tm1b(EUCOMM)Wtsi>/Adss2<+>	C57BL/6N-Adss2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6261821	F	MP:0005012	decreased eosinophil cell number	Adss2<tm1b(EUCOMM)Wtsi>/Adss2<+>	C57BL/6N-Adss2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6261826	M	MP:0008259	abnormal optic disk morphology	Ahsa1<em1(IMPC)J>/Ahsa1<em1(IMPC)J>	C57BL/6NJ-Ahsa1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261827	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Aicda<tm1b(EUCOMM)Hmgu>/Aicda<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aicda<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6261827	F	MP:0005561	increased mean corpuscular hemoglobin	Aicda<tm1b(EUCOMM)Hmgu>/Aicda<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aicda<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6261827	F	MP:0000218	increased leukocyte cell number	Aicda<tm1b(EUCOMM)Hmgu>/Aicda<tm1b(EUCOMM)Hmgu>	C57BL/6N-Aicda<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6261829	F	MP:0003795	abnormal bone structure	Akr7a5<tm1b(EUCOMM)Hmgu>/Akr7a5<+>	C57BL/6N-Akr7a5<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261831	M	MP:0000598	abnormal liver morphology	Alad<em1(IMPC)Tcp>/Alad<+>	C57BL/6NCrl-Alad<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261831	M	MP:0002768	small adrenal glands	Alad<em1(IMPC)Tcp>/Alad<+>	C57BL/6NCrl-Alad<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261831	F	MP:0000702	enlarged lymph nodes	Alad<em1(IMPC)Tcp>/Alad<+>	C57BL/6NCrl-Alad<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261831	M	MP:0011874	enlarged urinary bladder	Alad<em1(IMPC)Tcp>/Alad<+>	C57BL/6NCrl-Alad<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261831	M	MP:0000157	abnormal sternum morphology	Alad<em1(IMPC)Tcp>/Alad<+>	C57BL/6NCrl-Alad<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261831	F	MP:0002060	abnormal skin morphology	Alad<em1(IMPC)Tcp>/Alad<+>	C57BL/6NCrl-Alad<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261831	M	MP:0002059	abnormal seminal vesicle morphology	Alad<em1(IMPC)Tcp>/Alad<+>	C57BL/6NCrl-Alad<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261831	M	MP:0010053	decreased grip strength	Alad<em1(IMPC)Tcp>/Alad<+>	C57BL/6NCrl-Alad<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261831	M	MP:0010068	decreased red blood cell distribution width	Alad<em1(IMPC)Tcp>/Alad<+>	C57BL/6NCrl-Alad<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261831	M	MP:0000709	enlarged thymus	Alad<em1(IMPC)Tcp>/Alad<+>	C57BL/6NCrl-Alad<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261834	F	MP:0001399	hyperactivity	Aldh1a3<tm1b(KOMP)Wtsi>/Aldh1a3<+>	B6N(Cg)-Aldh1a3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6261834	F	MP:0002968	increased circulating alkaline phosphatase level	Aldh1a3<tm1b(KOMP)Wtsi>/Aldh1a3<+>	B6N(Cg)-Aldh1a3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6261836	M	MP:0020870	decreased thigmotaxis	Aldoa<tm1.1(KOMP)Wtsi>/Aldoa<+>	C57BL/6N-Aldoa<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6261836	M	MP:0000221	decreased leukocyte cell number	Aldoa<tm1.1(KOMP)Wtsi>/Aldoa<+>	C57BL/6N-Aldoa<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6261836	M	MP:0011965	decreased total retina thickness	Aldoa<tm1.1(KOMP)Wtsi>/Aldoa<+>	C57BL/6N-Aldoa<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6261841	M	MP:0001726	abnormal allantois morphology	Alg6<em1(IMPC)Tcp>/Alg6<em1(IMPC)Tcp>	C57BL/6NCrl-Alg6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261841	M	MP:0003984	embryonic growth retardation	Alg6<em1(IMPC)Tcp>/Alg6<em1(IMPC)Tcp>	C57BL/6NCrl-Alg6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261841	M	MP:0001672	abnormal embryo development	Alg6<em1(IMPC)Tcp>/Alg6<em1(IMPC)Tcp>	C57BL/6NCrl-Alg6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261841	M	MP:0001697	abnormal embryo size	Alg6<em1(IMPC)Tcp>/Alg6<em1(IMPC)Tcp>	C57BL/6NCrl-Alg6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261842	M	MP:0010124	decreased bone mineral content	Alg8<em1(IMPC)J>/Alg8<+>	C57BL/6NJ-Alg8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261842	M	MP:0001399	hyperactivity	Alg8<em1(IMPC)J>/Alg8<+>	C57BL/6NJ-Alg8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261842	M	MP:0001556	increased circulating HDL cholesterol level	Alg8<em1(IMPC)J>/Alg8<+>	C57BL/6NJ-Alg8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261842	M	MP:0005178	increased circulating cholesterol level	Alg8<em1(IMPC)J>/Alg8<+>	C57BL/6NJ-Alg8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261842	M	MP:0010024	increased total body fat amount	Alg8<em1(IMPC)J>/Alg8<+>	C57BL/6NJ-Alg8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261842	M	MP:0003961	decreased lean body mass	Alg8<em1(IMPC)J>/Alg8<+>	C57BL/6NJ-Alg8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261842	F	MP:0002098	abnormal vibrissa morphology	Alg8<em1(IMPC)J>/Alg8<+>	C57BL/6NJ-Alg8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261843	F	MP:0001697	abnormal embryo size	Alg8<em1(IMPC)J>/Alg8<em1(IMPC)J>	C57BL/6NJ-Alg8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261844	M	MP:0001529	abnormal vocalization	Alg9<em1(IMPC)J>/Alg9<+>	C57BL/6NJ-Alg9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261846	M	MP:0002581	abnormal ileum morphology	Alkbh1<tm1b(EUCOMM)Hmgu>/Alkbh1<+>	C57BL/6N-Alkbh1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261846	F	MP:0013678	decreased Ly6C-positive NK T cell number	Alkbh1<tm1b(EUCOMM)Hmgu>/Alkbh1<+>	C57BL/6N-Alkbh1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261846	F	MP:0000627	abnormal mammary gland morphology	Alkbh1<tm1b(EUCOMM)Hmgu>/Alkbh1<+>	C57BL/6N-Alkbh1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261846	F	MP:0008524	increased plasmacytoid dendritic cell number	Alkbh1<tm1b(EUCOMM)Hmgu>/Alkbh1<+>	C57BL/6N-Alkbh1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261846	M	MP:0000689	abnormal spleen morphology	Alkbh1<tm1b(EUCOMM)Hmgu>/Alkbh1<+>	C57BL/6N-Alkbh1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261846	M	MP:0002135	abnormal kidney morphology	Alkbh1<tm1b(EUCOMM)Hmgu>/Alkbh1<+>	C57BL/6N-Alkbh1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261846	F	MP:0000598	abnormal liver morphology	Alkbh1<tm1b(EUCOMM)Hmgu>/Alkbh1<+>	C57BL/6N-Alkbh1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261848	F	MP:0002092	abnormal eye morphology	Alkbh6<tm1b(EUCOMM)Hmgu>/Alkbh6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Alkbh6<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261848	M	MP:0002941	increased circulating alanine transaminase level	Alkbh6<tm1b(EUCOMM)Hmgu>/Alkbh6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Alkbh6<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261849	M	MP:0002599	increased mean platelet volume	Alkbh8<tm1b(EUCOMM)Hmgu>/Alkbh8<tm1b(EUCOMM)Hmgu>	C57BL/6N-Alkbh8<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261849	F	MP:0002968	increased circulating alkaline phosphatase level	Alkbh8<tm1b(EUCOMM)Hmgu>/Alkbh8<tm1b(EUCOMM)Hmgu>	C57BL/6N-Alkbh8<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261849	M	MP:0002135	abnormal kidney morphology	Alkbh8<tm1b(EUCOMM)Hmgu>/Alkbh8<tm1b(EUCOMM)Hmgu>	C57BL/6N-Alkbh8<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261850	M	MP:0001392	abnormal locomotor behavior	Alms1<tm1b(EUCOMM)Hmgu>/Alms1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Alms1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6261850	M	MP:0008806	increased circulating amylase level	Alms1<tm1b(EUCOMM)Hmgu>/Alms1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Alms1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6261851	F	MP:0001102	small superior vagus ganglion	Alox15<tm1b(KOMP)Mbp>/Alox15<tm1b(KOMP)Mbp>	C57BL/6N-Alox15<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6261851	M	MP:0001289	persistence of hyaloid vascular system	Alox15<tm1b(KOMP)Mbp>/Alox15<tm1b(KOMP)Mbp>	C57BL/6N-Alox15<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6261851	F	MP:0009709	hydrometra	Alox15<tm1b(KOMP)Mbp>/Alox15<tm1b(KOMP)Mbp>	C57BL/6N-Alox15<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6261851	F	MP:0011110	preweaning lethality, incomplete penetrance	Alox15<tm1b(KOMP)Mbp>/Alox15<tm1b(KOMP)Mbp>	C57BL/6N-Alox15<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6261853	M	MP:0010024	increased total body fat amount	Alpk2<em1(IMPC)J>/Alpk2<em1(IMPC)J>	C57BL/6NJ-Alpk2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261853	M	MP:0003961	decreased lean body mass	Alpk2<em1(IMPC)J>/Alpk2<em1(IMPC)J>	C57BL/6NJ-Alpk2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261853	M	MP:0010124	decreased bone mineral content	Alpk2<em1(IMPC)J>/Alpk2<em1(IMPC)J>	C57BL/6NJ-Alpk2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261853	F	MP:0009142	decreased prepulse inhibition	Alpk2<em1(IMPC)J>/Alpk2<em1(IMPC)J>	C57BL/6NJ-Alpk2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261854	F	MP:0002574	increased vertical activity	Amigo1<tm1.1(KOMP)Vlcg>/Amigo1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Amigo1<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:6261855	F	MP:0005627	increased circulating potassium level	Ampd2<tm1b(EUCOMM)Hmgu>/Ampd2<+>	C57BL/6N-Ampd2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6261859	M	MP:0000702	enlarged lymph nodes	Angpt2<em1(IMPC)Mbp>/Angpt2<em1(IMPC)Mbp>	C57BL/6NCrl-Angpt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261859	M	MP:0000706	small thymus	Angpt2<em1(IMPC)Mbp>/Angpt2<em1(IMPC)Mbp>	C57BL/6NCrl-Angpt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261859	M	MP:0000703	abnormal thymus morphology	Angpt2<em1(IMPC)Mbp>/Angpt2<em1(IMPC)Mbp>	C57BL/6NCrl-Angpt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261859	M	MP:0001157	small seminal vesicle	Angpt2<em1(IMPC)Mbp>/Angpt2<em1(IMPC)Mbp>	C57BL/6NCrl-Angpt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261859	M	MP:0002339	abnormal lymph node morphology	Angpt2<em1(IMPC)Mbp>/Angpt2<em1(IMPC)Mbp>	C57BL/6NCrl-Angpt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261860	M	MP:0008806	increased circulating amylase level	Ankhd1<tm1a(KOMP)Wtsi>/Ankhd1<tm1a(KOMP)Wtsi>	C57BL/6N-Ankhd1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261860	M	MP:0002079	increased circulating insulin level	Ankhd1<tm1a(KOMP)Wtsi>/Ankhd1<tm1a(KOMP)Wtsi>	C57BL/6N-Ankhd1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261861	F	MP:0001402	decreased locomotor activity	Ankle1<tm1(KOMP)Wtsi>/Ankle1<tm1(KOMP)Wtsi>	C57BL/6N-Ankle1<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6261862	F	MP:0010053	decreased grip strength	Ankrd10<tm2b(EUCOMM)Hmgu>/Ankrd10<+>	C57BL/6N-Ankrd10<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261862	F	MP:0011965	decreased total retina thickness	Ankrd10<tm2b(EUCOMM)Hmgu>/Ankrd10<+>	C57BL/6N-Ankrd10<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261867	F	MP:0010123	increased bone mineral content	Ankub1<tm1.1(KOMP)Vlcg>/Ankub1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ankub1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261868	M	MP:0002942	decreased circulating alanine transaminase level	Ano3<em2(IMPC)Mbp>/Ano3<em2(IMPC)Mbp>	C57BL/6N-Ano3<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261869	M	MP:0000702	enlarged lymph nodes	Ano6<em3(IMPC)Tcp>/Ano6<+>	C57BL/6NCrl-Ano6<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261869	F	MP:0005278	abnormal cholesterol homeostasis	Ano6<em3(IMPC)Tcp>/Ano6<+>	C57BL/6NCrl-Ano6<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261869	M	MP:0011954	shortened PQ interval	Ano6<em3(IMPC)Tcp>/Ano6<+>	C57BL/6NCrl-Ano6<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261871	F	MP:0000367	abnormal coat/ hair morphology	Ano7<em1(IMPC)J>/Ano7<em1(IMPC)J>	C57BL/6NJ-Ano7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261872	M	MP:0010124	decreased bone mineral content	Ano8<em1(IMPC)J>/Ano8<+>	C57BL/6NJ-Ano8<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261872	F	MP:0001399	hyperactivity	Ano8<em1(IMPC)J>/Ano8<+>	C57BL/6NJ-Ano8<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261875	F	MP:0003961	decreased lean body mass	Ap1g1<tm1b(EUCOMM)Hmgu>/Ap1g1<+>	B6N(Cg)-Ap1g1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6261875	M	MP:0001304	cataract	Ap1g1<tm1b(EUCOMM)Hmgu>/Ap1g1<+>	B6N(Cg)-Ap1g1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6261875	F	MP:0010024	increased total body fat amount	Ap1g1<tm1b(EUCOMM)Hmgu>/Ap1g1<+>	B6N(Cg)-Ap1g1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6261875	F	MP:0002574	increased vertical activity	Ap1g1<tm1b(EUCOMM)Hmgu>/Ap1g1<+>	B6N(Cg)-Ap1g1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6261875	F	MP:0010124	decreased bone mineral content	Ap1g1<tm1b(EUCOMM)Hmgu>/Ap1g1<+>	B6N(Cg)-Ap1g1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6261875	F	MP:0001325	abnormal retina morphology	Ap1g1<tm1b(EUCOMM)Hmgu>/Ap1g1<+>	B6N(Cg)-Ap1g1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6261877	M	MP:0000182	increased circulating LDL cholesterol level	Ap2a2<em1(IMPC)Wtsi>/Ap2a2<+>	C57BL/6N-Ap2a2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261877	M	MP:0005178	increased circulating cholesterol level	Ap2a2<em1(IMPC)Wtsi>/Ap2a2<+>	C57BL/6N-Ap2a2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261877	M	MP:0001556	increased circulating HDL cholesterol level	Ap2a2<em1(IMPC)Wtsi>/Ap2a2<+>	C57BL/6N-Ap2a2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261880	F	MP:0001258	decreased body length	Ap2s1<em1(IMPC)Tcp>/Ap2s1<+>	C57BL/6NCrl-Ap2s1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261880	M	MP:0009476	enlarged cecum	Ap2s1<em1(IMPC)Tcp>/Ap2s1<+>	C57BL/6NCrl-Ap2s1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261880	F	MP:0000274	enlarged heart	Ap2s1<em1(IMPC)Tcp>/Ap2s1<+>	C57BL/6NCrl-Ap2s1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261880	F	MP:0009709	hydrometra	Ap2s1<em1(IMPC)Tcp>/Ap2s1<+>	C57BL/6NCrl-Ap2s1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261880	F	MP:0000266	abnormal heart morphology	Ap2s1<em1(IMPC)Tcp>/Ap2s1<+>	C57BL/6NCrl-Ap2s1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261880	M	MP:0000494	abnormal cecum morphology	Ap2s1<em1(IMPC)Tcp>/Ap2s1<+>	C57BL/6NCrl-Ap2s1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261880	F	MP:0001102	small superior vagus ganglion	Ap2s1<em1(IMPC)Tcp>/Ap2s1<+>	C57BL/6NCrl-Ap2s1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261881	F	MP:0011396	abnormal sleep behavior	Ap4e1<em1(IMPC)J>/Ap4e1<+>	C57BL/6NJ-Ap4e1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261881	M	MP:0001554	increased circulating free fatty acids level	Ap4e1<em1(IMPC)J>/Ap4e1<+>	C57BL/6NJ-Ap4e1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261881	F	MP:0005560	decreased circulating glucose level	Ap4e1<em1(IMPC)J>/Ap4e1<+>	C57BL/6NJ-Ap4e1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261882	M	MP:0002702	decreased circulating free fatty acids level	Ap4e1<em1(IMPC)J>/Ap4e1<em1(IMPC)J>	C57BL/6NJ-Ap4e1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261882	F	MP:0001513	limb grasping	Ap4e1<em1(IMPC)J>/Ap4e1<em1(IMPC)J>	C57BL/6NJ-Ap4e1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261882	F	MP:0002757	decreased vertical activity	Ap4e1<em1(IMPC)J>/Ap4e1<em1(IMPC)J>	C57BL/6NJ-Ap4e1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261883	F	MP:0005278	abnormal cholesterol homeostasis	Ap4e1<em2(IMPC)Mbp>/Ap4e1<em2(IMPC)Mbp>	C57BL/6NCrl-Ap4e1<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261883	F	MP:0005343	increased circulating aspartate transaminase level	Ap4e1<em2(IMPC)Mbp>/Ap4e1<em2(IMPC)Mbp>	C57BL/6NCrl-Ap4e1<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261884	M	MP:0001510	abnormal coat appearance	Apeh<tm2b(EUCOMM)Hmgu>/Apeh<tm2b(EUCOMM)Hmgu>	C57BL/6N-Apeh<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6261884	M	MP:0009142	decreased prepulse inhibition	Apeh<tm2b(EUCOMM)Hmgu>/Apeh<tm2b(EUCOMM)Hmgu>	C57BL/6N-Apeh<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6261886	M	MP:0002092	abnormal eye morphology	Aplnr<tm1.1(KOMP)Vlcg>/Aplnr<tm1.1(KOMP)Vlcg>	C57BL/6N-Aplnr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261886	M	MP:0002135	abnormal kidney morphology	Aplnr<tm1.1(KOMP)Vlcg>/Aplnr<tm1.1(KOMP)Vlcg>	C57BL/6N-Aplnr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261886	M	MP:0002631	abnormal epididymis morphology	Aplnr<tm1.1(KOMP)Vlcg>/Aplnr<tm1.1(KOMP)Vlcg>	C57BL/6N-Aplnr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261887	M	MP:0000367	abnormal coat/ hair morphology	Apof<tm1.1(KOMP)Vlcg>/Apof<tm1.1(KOMP)Vlcg>	C57BL/6N-Apof<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261887	M	MP:0002606	increased basophil cell number	Apof<tm1.1(KOMP)Vlcg>/Apof<tm1.1(KOMP)Vlcg>	C57BL/6N-Apof<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261888	F	MP:0001304	cataract	Aptx<tm1b(EUCOMM)Hmgu>/Aptx<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Aptx<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6261888	M	MP:0010124	decreased bone mineral content	Aptx<tm1b(EUCOMM)Hmgu>/Aptx<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Aptx<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6261888	F	MP:0000063	decreased bone mineral density	Aptx<tm1b(EUCOMM)Hmgu>/Aptx<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Aptx<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6261888	M	MP:0002941	increased circulating alanine transaminase level	Aptx<tm1b(EUCOMM)Hmgu>/Aptx<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Aptx<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6261889	F	MP:0005343	increased circulating aspartate transaminase level	Aqp12<tm1.1(KOMP)Vlcg>/Aqp12<tm1.1(KOMP)Vlcg>	C57BL/6N-Aqp12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261890	M	MP:0001529	abnormal vocalization	Arap1<tm1b(EUCOMM)Wtsi>/Arap1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arap1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6261890	M	MP:0005562	decreased mean corpuscular hemoglobin	Arap1<tm1b(EUCOMM)Wtsi>/Arap1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arap1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6261890	F	MP:0002764	short tibia	Arap1<tm1b(EUCOMM)Wtsi>/Arap1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arap1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6261891	M	MP:0006243	impaired pupillary reflex	Arap3<em1(IMPC)J>/Arap3<em1(IMPC)J>	C57BL/6NJ-Arap3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261891	M	MP:0020870	decreased thigmotaxis	Arap3<em1(IMPC)J>/Arap3<em1(IMPC)J>	C57BL/6NJ-Arap3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261891	F	MP:0002098	abnormal vibrissa morphology	Arap3<em1(IMPC)J>/Arap3<em1(IMPC)J>	C57BL/6NJ-Arap3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261891	F	MP:0001399	hyperactivity	Arap3<em1(IMPC)J>/Arap3<em1(IMPC)J>	C57BL/6NJ-Arap3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261891	M	MP:0001304	cataract	Arap3<em1(IMPC)J>/Arap3<em1(IMPC)J>	C57BL/6NJ-Arap3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261892	M	MP:0011110	preweaning lethality, incomplete penetrance	Arhgap19<tm1b(KOMP)Wtsi>/Arhgap19<tm1b(KOMP)Wtsi>	C57BL/6N-Arhgap19<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6261892	M	MP:0000274	enlarged heart	Arhgap19<tm1b(KOMP)Wtsi>/Arhgap19<tm1b(KOMP)Wtsi>	C57BL/6N-Arhgap19<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6261892	M	MP:0000266	abnormal heart morphology	Arhgap19<tm1b(KOMP)Wtsi>/Arhgap19<tm1b(KOMP)Wtsi>	C57BL/6N-Arhgap19<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6261893	M	MP:0005343	increased circulating aspartate transaminase level	Arhgap29<em1(IMPC)J>/Arhgap29<+>	C57BL/6NJ-Arhgap29<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261893	M	MP:0002941	increased circulating alanine transaminase level	Arhgap29<em1(IMPC)J>/Arhgap29<+>	C57BL/6NJ-Arhgap29<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261895	M	MP:0000221	decreased leukocyte cell number	Arhgap30<tm1a(EUCOMM)Wtsi>/Arhgap30<tm1a(EUCOMM)Wtsi>	C57BL/6N-Arhgap30<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261896	M	MP:0001289	persistence of hyaloid vascular system	Arhgap44<em1(IMPC)J>/Arhgap44<em1(IMPC)J>	C57BL/6NJ-Arhgap44<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261897	F	MP:0001304	cataract	Arhgap8<em1(IMPC)J>/Arhgap8<em1(IMPC)J>	C57BL/6NJ-Arhgap8<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261897	F	MP:0002574	increased vertical activity	Arhgap8<em1(IMPC)J>/Arhgap8<em1(IMPC)J>	C57BL/6NJ-Arhgap8<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261898	F	MP:0008806	increased circulating amylase level	Arhgef18<tm1b(KOMP)Mbp>/Arhgef18<+>	C57BL/6N-Arhgef18<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6261901	F	MP:0009142	decreased prepulse inhibition	Arid1b<em1(IMPC)Tcp>/Arid1b<+>	C57BL/6NCrl-Arid1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261901	F	MP:0001417	decreased exploration in new environment	Arid1b<em1(IMPC)Tcp>/Arid1b<+>	C57BL/6NCrl-Arid1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261901	M	MP:0000689	abnormal spleen morphology	Arid1b<em1(IMPC)Tcp>/Arid1b<+>	C57BL/6NCrl-Arid1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261901	M	MP:0013278	decreased fasting circulating glucose level	Arid1b<em1(IMPC)Tcp>/Arid1b<+>	C57BL/6NCrl-Arid1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261901	F	MP:0009456	impaired cued conditioning behavior	Arid1b<em1(IMPC)Tcp>/Arid1b<+>	C57BL/6NCrl-Arid1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261901	F	MP:0020421	increased freezing behavior	Arid1b<em1(IMPC)Tcp>/Arid1b<+>	C57BL/6NCrl-Arid1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261901	F	MP:0020420	abnormal freezing behavior	Arid1b<em1(IMPC)Tcp>/Arid1b<+>	C57BL/6NCrl-Arid1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261903	M	MP:0001925	male infertility	Arid1b<tm1b(EUCOMM)Hmgu>/Arid1b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Arid1b<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6261909	F	MP:0000691	enlarged spleen	Armh4<em1(IMPC)H>/Armh4<em1(IMPC)H>	C57BL/6N-Armh4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261909	F	MP:0010052	increased grip strength	Armh4<em1(IMPC)H>/Armh4<em1(IMPC)H>	C57BL/6N-Armh4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261909	M	MP:0001406	abnormal gait	Armh4<em1(IMPC)H>/Armh4<em1(IMPC)H>	C57BL/6N-Armh4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6261912	F	MP:0002968	increased circulating alkaline phosphatase level	Arr3<em1(IMPC)J>/Arr3<em1(IMPC)J>	C57BL/6NJ-Arr3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261912	F	MP:0002644	decreased circulating triglyceride level	Arr3<em1(IMPC)J>/Arr3<em1(IMPC)J>	C57BL/6NJ-Arr3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261913	F	MP:0001325	abnormal retina morphology	Arrdc5<tm1b(EUCOMM)Wtsi>/Arrdc5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arrdc5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261913	M	MP:0010087	increased circulating fructosamine level	Arrdc5<tm1b(EUCOMM)Wtsi>/Arrdc5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arrdc5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261913	F	MP:0005561	increased mean corpuscular hemoglobin	Arrdc5<tm1b(EUCOMM)Wtsi>/Arrdc5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arrdc5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261913	F	MP:0002968	increased circulating alkaline phosphatase level	Arrdc5<tm1b(EUCOMM)Wtsi>/Arrdc5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arrdc5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261913	M	MP:0001925	male infertility	Arrdc5<tm1b(EUCOMM)Wtsi>/Arrdc5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arrdc5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261914	M	MP:0010053	decreased grip strength	Art1<tm1b(EUCOMM)Wtsi>/Art1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Art1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261914	M	MP:0000702	enlarged lymph nodes	Art1<tm1b(EUCOMM)Wtsi>/Art1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Art1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261914	M	MP:0001417	decreased exploration in new environment	Art1<tm1b(EUCOMM)Wtsi>/Art1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Art1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261914	M	MP:0002606	increased basophil cell number	Art1<tm1b(EUCOMM)Wtsi>/Art1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Art1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261914	M	MP:0005634	decreased circulating sodium level	Art1<tm1b(EUCOMM)Wtsi>/Art1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Art1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261914	M	MP:0002941	increased circulating alanine transaminase level	Art1<tm1b(EUCOMM)Wtsi>/Art1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Art1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261914	M	MP:0000195	decreased circulating calcium level	Art1<tm1b(EUCOMM)Wtsi>/Art1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Art1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261914	F	MP:0002060	abnormal skin morphology	Art1<tm1b(EUCOMM)Wtsi>/Art1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Art1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261915	M	MP:0011239	abnormal skin coloration	Ash2l<tm1b(EUCOMM)Wtsi>/Ash2l<+>	C57BL/6N-Ash2l<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6261919	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Aspg<em1(IMPC)Tcp>/Aspg<em1(IMPC)Tcp>	C57BL/6NCrl-Aspg<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261919	F	MP:0002060	abnormal skin morphology	Aspg<em1(IMPC)Tcp>/Aspg<em1(IMPC)Tcp>	C57BL/6NCrl-Aspg<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261919	F	MP:0002591	decreased mean corpuscular volume	Aspg<em1(IMPC)Tcp>/Aspg<em1(IMPC)Tcp>	C57BL/6NCrl-Aspg<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261920	M	MP:0000702	enlarged lymph nodes	Aspscr1<em1(IMPC)Tcp>/Aspscr1<em1(IMPC)Tcp>	C57BL/6NCrl-Aspscr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261920	M	MP:0000222	decreased neutrophil cell number	Aspscr1<em1(IMPC)Tcp>/Aspscr1<em1(IMPC)Tcp>	C57BL/6NCrl-Aspscr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261920	M	MP:0000494	abnormal cecum morphology	Aspscr1<em1(IMPC)Tcp>/Aspscr1<em1(IMPC)Tcp>	C57BL/6NCrl-Aspscr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261920	F	MP:0000598	abnormal liver morphology	Aspscr1<em1(IMPC)Tcp>/Aspscr1<em1(IMPC)Tcp>	C57BL/6NCrl-Aspscr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261920	M	MP:0005013	increased lymphocyte cell number	Aspscr1<em1(IMPC)Tcp>/Aspscr1<em1(IMPC)Tcp>	C57BL/6NCrl-Aspscr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261920	M	MP:0001417	decreased exploration in new environment	Aspscr1<em1(IMPC)Tcp>/Aspscr1<em1(IMPC)Tcp>	C57BL/6NCrl-Aspscr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261920	M	MP:0020421	increased freezing behavior	Aspscr1<em1(IMPC)Tcp>/Aspscr1<em1(IMPC)Tcp>	C57BL/6NCrl-Aspscr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261922	F	MP:0002764	short tibia	Atg13<tm2b(EUCOMM)Hmgu>/Atg13<+>	C57BL/6N-Atg13<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6261924	F	MP:0002941	increased circulating alanine transaminase level	Atg9b<tm1b(KOMP)Mbp>/Atg9b<tm1b(KOMP)Mbp>	C57BL/6N-Atg9b<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6261924	F	MP:0002092	abnormal eye morphology	Atg9b<tm1b(KOMP)Mbp>/Atg9b<tm1b(KOMP)Mbp>	C57BL/6N-Atg9b<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6261924	F	MP:0001333	absent optic nerve	Atg9b<tm1b(KOMP)Mbp>/Atg9b<tm1b(KOMP)Mbp>	C57BL/6N-Atg9b<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6261924	F	MP:0001293	anophthalmia	Atg9b<tm1b(KOMP)Mbp>/Atg9b<tm1b(KOMP)Mbp>	C57BL/6N-Atg9b<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6261926	M	MP:0000157	abnormal sternum morphology	Atp2c2<em1(IMPC)Tcp>/Atp2c2<em1(IMPC)Tcp>	C57BL/6NCrl-Atp2c2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261926	M	MP:0002059	abnormal seminal vesicle morphology	Atp2c2<em1(IMPC)Tcp>/Atp2c2<em1(IMPC)Tcp>	C57BL/6NCrl-Atp2c2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261926	M	MP:0000208	decreased hematocrit	Atp2c2<em1(IMPC)Tcp>/Atp2c2<em1(IMPC)Tcp>	C57BL/6NCrl-Atp2c2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261926	M	MP:0000702	enlarged lymph nodes	Atp2c2<em1(IMPC)Tcp>/Atp2c2<em1(IMPC)Tcp>	C57BL/6NCrl-Atp2c2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261928	M	MP:0010067	increased red blood cell distribution width	Atp5f1e<tm1b(EUCOMM)Wtsi>/Atp5f1e<+>	C57BL/6N-Atp5f1e<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261929	M	MP:0005292	improved glucose tolerance	Atp5po<tm1.1(KOMP)Vlcg>/Atp5po<+>	B6N(Cg)-Atp5po<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6261931	F	MP:0002941	increased circulating alanine transaminase level	Atp6v1b1<tm1.1(KOMP)Vlcg>/Atp6v1b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Atp6v1b1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261934	M	MP:0002834	decreased heart weight	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0002092	abnormal eye morphology	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0005343	increased circulating aspartate transaminase level	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	F	MP:0003795	abnormal bone structure	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	F	MP:0000691	enlarged spleen	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0002941	increased circulating alanine transaminase level	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0005333	decreased heart rate	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0001489	decreased startle reflex	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	F	MP:0005627	increased circulating potassium level	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0002631	abnormal epididymis morphology	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0010052	increased grip strength	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0011874	enlarged urinary bladder	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	F	MP:0001293	anophthalmia	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0000186	decreased circulating HDL cholesterol level	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0002591	decreased mean corpuscular volume	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0003068	enlarged kidney	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0001157	small seminal vesicle	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	F	MP:0005344	increased circulating bilirubin level	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0010506	prolonged RR interval	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261934	M	MP:0004357	long tibia	Atp8b1<em1(IMPC)Tcp>/Atp8b1<em1(IMPC)Tcp>	C57BL/6NCrl-Atp8b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261935	F	MP:0001399	hyperactivity	Atp9a<tm1b(EUCOMM)Hmgu>/Atp9a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atp9a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261935	F	MP:0001415	increased exploration in new environment	Atp9a<tm1b(EUCOMM)Hmgu>/Atp9a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atp9a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261937	F	MP:0010053	decreased grip strength	Atrn<tm1.1(KOMP)Vlcg>/Atrn<tm1.1(KOMP)Vlcg>	C57BL/6N-Atrn<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261937	M	MP:0010123	increased bone mineral content	Atrn<tm1.1(KOMP)Vlcg>/Atrn<tm1.1(KOMP)Vlcg>	C57BL/6N-Atrn<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261937	M	MP:0002092	abnormal eye morphology	Atrn<tm1.1(KOMP)Vlcg>/Atrn<tm1.1(KOMP)Vlcg>	C57BL/6N-Atrn<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261938	F	MP:0010123	increased bone mineral content	Atxn7l2<em1(IMPC)Mbp>/Atxn7l2<em1(IMPC)Mbp>	C57BL/6NCrl-Atxn7l2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261938	F	MP:0002092	abnormal eye morphology	Atxn7l2<em1(IMPC)Mbp>/Atxn7l2<em1(IMPC)Mbp>	C57BL/6NCrl-Atxn7l2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261938	F	MP:0000194	increased circulating calcium level	Atxn7l2<em1(IMPC)Mbp>/Atxn7l2<em1(IMPC)Mbp>	C57BL/6NCrl-Atxn7l2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261939	M	MP:0002075	abnormal coat/hair pigmentation	AU040320<em1(IMPC)J>/AU040320<em1(IMPC)J>	C57BL/6NJ-AU040320<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261939	M	MP:0001925	male infertility	AU040320<em1(IMPC)J>/AU040320<em1(IMPC)J>	C57BL/6NJ-AU040320<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261939	F	MP:0010053	decreased grip strength	AU040320<em1(IMPC)J>/AU040320<em1(IMPC)J>	C57BL/6NJ-AU040320<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261939	M	MP:0000063	decreased bone mineral density	AU040320<em1(IMPC)J>/AU040320<em1(IMPC)J>	C57BL/6NJ-AU040320<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261939	F	MP:0010024	increased total body fat amount	AU040320<em1(IMPC)J>/AU040320<em1(IMPC)J>	C57BL/6NJ-AU040320<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261939	F	MP:0001415	increased exploration in new environment	AU040320<em1(IMPC)J>/AU040320<em1(IMPC)J>	C57BL/6NJ-AU040320<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261939	F	MP:0003961	decreased lean body mass	AU040320<em1(IMPC)J>/AU040320<em1(IMPC)J>	C57BL/6NJ-AU040320<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261939	M	MP:0001486	abnormal startle reflex	AU040320<em1(IMPC)J>/AU040320<em1(IMPC)J>	C57BL/6NJ-AU040320<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261940	M	MP:0005011	increased eosinophil cell number	Auh<em1(IMPC)Tcp>/Auh<em1(IMPC)Tcp>	C57BL/6NCrl-Auh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261940	M	MP:0002941	increased circulating alanine transaminase level	Auh<em1(IMPC)Tcp>/Auh<em1(IMPC)Tcp>	C57BL/6NCrl-Auh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261940	M	MP:0000157	abnormal sternum morphology	Auh<em1(IMPC)Tcp>/Auh<em1(IMPC)Tcp>	C57BL/6NCrl-Auh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261941	F	MP:0001258	decreased body length	Auts2<em1(IMPC)Wtsi>/Auts2<+>	C57BL/6N-Auts2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261943	M	MP:0010124	decreased bone mineral content	B3galnt2<em1(IMPC)J>/B3galnt2<+>	C57BL/6NJ-B3galnt2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261945	F	MP:0002989	small kidney	B3galt2<tm1.1(KOMP)Vlcg>/B3galt2<+>	C57BL/6N-B3galt2<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6261945	F	MP:0010123	increased bone mineral content	B3galt2<tm1.1(KOMP)Vlcg>/B3galt2<+>	C57BL/6N-B3galt2<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6261945	F	MP:0002135	abnormal kidney morphology	B3galt2<tm1.1(KOMP)Vlcg>/B3galt2<+>	C57BL/6N-B3galt2<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6261947	F	MP:0002092	abnormal eye morphology	B3galt6<em2(IMPC)Tcp>/B3galt6<+>	C57BL/6NCrl-B3galt6<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261949	M	MP:0002339	abnormal lymph node morphology	Baat<em1(IMPC)Mbp>/Baat<em1(IMPC)Mbp>	C57BL/6NCrl-Baat<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261949	M	MP:0005179	decreased circulating cholesterol level	Baat<em1(IMPC)Mbp>/Baat<em1(IMPC)Mbp>	C57BL/6NCrl-Baat<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261949	M	MP:0000266	abnormal heart morphology	Baat<em1(IMPC)Mbp>/Baat<em1(IMPC)Mbp>	C57BL/6NCrl-Baat<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261949	M	MP:0000274	enlarged heart	Baat<em1(IMPC)Mbp>/Baat<em1(IMPC)Mbp>	C57BL/6NCrl-Baat<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261949	M	MP:0005292	improved glucose tolerance	Baat<em1(IMPC)Mbp>/Baat<em1(IMPC)Mbp>	C57BL/6NCrl-Baat<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261949	M	MP:0000186	decreased circulating HDL cholesterol level	Baat<em1(IMPC)Mbp>/Baat<em1(IMPC)Mbp>	C57BL/6NCrl-Baat<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261949	M	MP:0001552	increased circulating triglyceride level	Baat<em1(IMPC)Mbp>/Baat<em1(IMPC)Mbp>	C57BL/6NCrl-Baat<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261949	F	MP:0002590	increased mean corpuscular volume	Baat<em1(IMPC)Mbp>/Baat<em1(IMPC)Mbp>	C57BL/6NCrl-Baat<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261950	F	MP:0013513	decreased memory-marker CD4-negative NK T cell number	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	F	MP:0000063	decreased bone mineral density	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	M	MP:0000220	increased monocyte cell number	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	M	MP:0001513	limb grasping	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	M	MP:0000322	increased granulocyte number	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	F	MP:0005011	increased eosinophil cell number	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	F	MP:0008168	decreased B-1a cell number	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	F	MP:0013675	decreased Ly6C-positive mature NK cell number	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	M	MP:0001417	decreased exploration in new environment	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	F	MP:0005343	increased circulating aspartate transaminase level	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	F	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	M	MP:0010052	increased grip strength	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	F	MP:0008190	decreased transitional stage B cell number	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	F	MP:0013669	decreased Ly6C-positive immature NK cell number	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	F	MP:0008040	decreased NK T cell number	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	M	MP:0002968	increased circulating alkaline phosphatase level	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	F	MP:0002764	short tibia	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	M	MP:0008039	increased NK T cell number	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261950	M	MP:0008806	increased circulating amylase level	Bach2<tm1b(EUCOMM)Wtsi>/Bach2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bach2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6261951	M	MP:0011110	preweaning lethality, incomplete penetrance	Bambi<tm1.1(KOMP)Vlcg>/Bambi<tm1.1(KOMP)Vlcg>	C57BL/6N-Bambi<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261951	F	MP:0009709	hydrometra	Bambi<tm1.1(KOMP)Vlcg>/Bambi<tm1.1(KOMP)Vlcg>	C57BL/6N-Bambi<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261951	M	MP:0001146	abnormal testis morphology	Bambi<tm1.1(KOMP)Vlcg>/Bambi<tm1.1(KOMP)Vlcg>	C57BL/6N-Bambi<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261951	M	MP:0001147	small testis	Bambi<tm1.1(KOMP)Vlcg>/Bambi<tm1.1(KOMP)Vlcg>	C57BL/6N-Bambi<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261951	F	MP:0001120	abnormal uterus morphology	Bambi<tm1.1(KOMP)Vlcg>/Bambi<tm1.1(KOMP)Vlcg>	C57BL/6N-Bambi<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261952	F	MP:0002060	abnormal skin morphology	Baz2a<em1(IMPC)Tcp>/Baz2a<em1(IMPC)Tcp>	C57BL/6NCrl-Baz2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261952	M	MP:0001147	small testis	Baz2a<em1(IMPC)Tcp>/Baz2a<em1(IMPC)Tcp>	C57BL/6NCrl-Baz2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261952	M	MP:0005565	increased blood urea nitrogen level	Baz2a<em1(IMPC)Tcp>/Baz2a<em1(IMPC)Tcp>	C57BL/6NCrl-Baz2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261952	M	MP:0005633	increased circulating sodium level	Baz2a<em1(IMPC)Tcp>/Baz2a<em1(IMPC)Tcp>	C57BL/6NCrl-Baz2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261952	M	MP:0004930	small epididymis	Baz2a<em1(IMPC)Tcp>/Baz2a<em1(IMPC)Tcp>	C57BL/6NCrl-Baz2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261952	F	MP:0000689	abnormal spleen morphology	Baz2a<em1(IMPC)Tcp>/Baz2a<em1(IMPC)Tcp>	C57BL/6NCrl-Baz2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261952	M	MP:0002989	small kidney	Baz2a<em1(IMPC)Tcp>/Baz2a<em1(IMPC)Tcp>	C57BL/6NCrl-Baz2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261953	F	MP:0010124	decreased bone mineral content	Baz2b<em1(IMPC)Wtsi>/Baz2b<em1(IMPC)Wtsi>	C57BL/6N-Baz2b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261953	M	MP:0003961	decreased lean body mass	Baz2b<em1(IMPC)Wtsi>/Baz2b<em1(IMPC)Wtsi>	C57BL/6N-Baz2b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261953	M	MP:0010024	increased total body fat amount	Baz2b<em1(IMPC)Wtsi>/Baz2b<em1(IMPC)Wtsi>	C57BL/6N-Baz2b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261953	F	MP:0000218	increased leukocyte cell number	Baz2b<em1(IMPC)Wtsi>/Baz2b<em1(IMPC)Wtsi>	C57BL/6N-Baz2b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261953	F	MP:0002075	abnormal coat/hair pigmentation	Baz2b<em1(IMPC)Wtsi>/Baz2b<em1(IMPC)Wtsi>	C57BL/6N-Baz2b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261953	F	MP:0002968	increased circulating alkaline phosphatase level	Baz2b<em1(IMPC)Wtsi>/Baz2b<em1(IMPC)Wtsi>	C57BL/6N-Baz2b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261953	M	MP:0005560	decreased circulating glucose level	Baz2b<em1(IMPC)Wtsi>/Baz2b<em1(IMPC)Wtsi>	C57BL/6N-Baz2b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261954	M	MP:0001925	male infertility	Bbox1<tm1a(KOMP)Wtsi>/Bbox1<tm1a(KOMP)Wtsi>	C57BL/6N-Bbox1<tm1a(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6261954	M	MP:0000274	enlarged heart	Bbox1<tm1a(KOMP)Wtsi>/Bbox1<tm1a(KOMP)Wtsi>	C57BL/6N-Bbox1<tm1a(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6261954	M	MP:0000266	abnormal heart morphology	Bbox1<tm1a(KOMP)Wtsi>/Bbox1<tm1a(KOMP)Wtsi>	C57BL/6N-Bbox1<tm1a(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6261956	M	MP:0020421	increased freezing behavior	BC048562<tm1b(KOMP)Wtsi>/BC048562<tm1b(KOMP)Wtsi>	C57BL/6N-BC048562<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6261956	M	MP:0013278	decreased fasting circulating glucose level	BC048562<tm1b(KOMP)Wtsi>/BC048562<tm1b(KOMP)Wtsi>	C57BL/6N-BC048562<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6261957	M	MP:0001486	abnormal startle reflex	Cdin1<em1(IMPC)J>/Cdin1<+>	C57BL/6NJ-Cdin1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261957	F	MP:0002941	increased circulating alanine transaminase level	Cdin1<em1(IMPC)J>/Cdin1<+>	C57BL/6NJ-Cdin1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6261959	M	MP:0001175	abnormal lung morphology	Bcas1<em1(IMPC)Tcp>/Bcas1<em1(IMPC)Tcp>	C57BL/6NCrl-Bcas1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261961	M	MP:0000219	increased neutrophil cell number	Bckdha<em1(IMPC)Tcp>/Bckdha<+>	C57BL/6NCrl-Bckdha<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261961	M	MP:0005016	decreased lymphocyte cell number	Bckdha<em1(IMPC)Tcp>/Bckdha<+>	C57BL/6NCrl-Bckdha<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261961	M	MP:0001157	small seminal vesicle	Bckdha<em1(IMPC)Tcp>/Bckdha<+>	C57BL/6NCrl-Bckdha<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6261962	M	MP:0010024	increased total body fat amount	Bckdhb<em1(IMPC)J>/Bckdhb<+>	C57BL/6NJ-Bckdhb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6261964	F	MP:0013279	increased fasting circulating glucose level	Bcl11b<tm1.1(KOMP)Vlcg>/Bcl11b<+>	B6N(Cg)-Bcl11b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6261964	F	MP:0003795	abnormal bone structure	Bcl11b<tm1.1(KOMP)Vlcg>/Bcl11b<+>	B6N(Cg)-Bcl11b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6261964	F	MP:0010123	increased bone mineral content	Bcl11b<tm1.1(KOMP)Vlcg>/Bcl11b<+>	B6N(Cg)-Bcl11b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6261965	M	MP:0003743	abnormal facial morphology	Bcl11b<tm1.1(KOMP)Vlcg>/Bcl11b<tm1.1(KOMP)Vlcg>	B6N(Cg)-Bcl11b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6261966	F	MP:0010123	increased bone mineral content	Bcl2l12<tm1.1(KOMP)Vlcg>/Bcl2l12<tm1.1(KOMP)Vlcg>	C57BL/6N-Bcl2l12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261966	M	MP:0000689	abnormal spleen morphology	Bcl2l12<tm1.1(KOMP)Vlcg>/Bcl2l12<tm1.1(KOMP)Vlcg>	C57BL/6N-Bcl2l12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261966	M	MP:0000691	enlarged spleen	Bcl2l12<tm1.1(KOMP)Vlcg>/Bcl2l12<tm1.1(KOMP)Vlcg>	C57BL/6N-Bcl2l12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261966	M	MP:0004952	increased spleen weight	Bcl2l12<tm1.1(KOMP)Vlcg>/Bcl2l12<tm1.1(KOMP)Vlcg>	C57BL/6N-Bcl2l12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261966	M	MP:0000598	abnormal liver morphology	Bcl2l12<tm1.1(KOMP)Vlcg>/Bcl2l12<tm1.1(KOMP)Vlcg>	C57BL/6N-Bcl2l12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261967	F	MP:0005344	increased circulating bilirubin level	Bcl2l15<tm1b(EUCOMM)Hmgu>/Bcl2l15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bcl2l15<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261967	M	MP:0005568	increased circulating total protein level	Bcl2l15<tm1b(EUCOMM)Hmgu>/Bcl2l15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bcl2l15<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261967	F	MP:0005562	decreased mean corpuscular hemoglobin	Bcl2l15<tm1b(EUCOMM)Hmgu>/Bcl2l15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bcl2l15<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261967	M	MP:0000598	abnormal liver morphology	Bcl2l15<tm1b(EUCOMM)Hmgu>/Bcl2l15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bcl2l15<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261967	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Bcl2l15<tm1b(EUCOMM)Hmgu>/Bcl2l15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bcl2l15<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261967	M	MP:0001417	decreased exploration in new environment	Bcl2l15<tm1b(EUCOMM)Hmgu>/Bcl2l15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bcl2l15<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261967	F	MP:0001488	increased startle reflex	Bcl2l15<tm1b(EUCOMM)Hmgu>/Bcl2l15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bcl2l15<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261967	F	MP:0002874	decreased hemoglobin content	Bcl2l15<tm1b(EUCOMM)Hmgu>/Bcl2l15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bcl2l15<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261967	M	MP:0000274	enlarged heart	Bcl2l15<tm1b(EUCOMM)Hmgu>/Bcl2l15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bcl2l15<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6261968	F	MP:0004952	increased spleen weight	Bcl3<tm1b(EUCOMM)Wtsi>/Bcl3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bcl3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6261969	F	MP:0001303	abnormal lens morphology	Bclaf1<tm1b(EUCOMM)Wtsi>/Bclaf1<+>	B6N(Cg)-Bclaf1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6261972	F	MP:0005344	increased circulating bilirubin level	Becn1<tm1b(KOMP)Wtsi>/Becn1<+>	C57BL/6N-Becn1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6261972	F	MP:0003961	decreased lean body mass	Becn1<tm1b(KOMP)Wtsi>/Becn1<+>	C57BL/6N-Becn1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6261972	M	MP:0001488	increased startle reflex	Becn1<tm1b(KOMP)Wtsi>/Becn1<+>	C57BL/6N-Becn1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6261972	M	MP:0000186	decreased circulating HDL cholesterol level	Becn1<tm1b(KOMP)Wtsi>/Becn1<+>	C57BL/6N-Becn1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6261972	F	MP:0010024	increased total body fat amount	Becn1<tm1b(KOMP)Wtsi>/Becn1<+>	C57BL/6N-Becn1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6261979	F	MP:0004906	enlarged uterus	Bfsp1<tm1b(EUCOMM)Wtsi>/Bfsp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bfsp1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261979	F	MP:0001102	small superior vagus ganglion	Bfsp1<tm1b(EUCOMM)Wtsi>/Bfsp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bfsp1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261979	M	MP:0001488	increased startle reflex	Bfsp1<tm1b(EUCOMM)Wtsi>/Bfsp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bfsp1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6261980	F	MP:0001258	decreased body length	Bgn<tm1.1(KOMP)Vlcg>/Bgn<tm1.1(KOMP)Vlcg>	C57BL/6N-Bgn<tm1.1(KOMP)Vlcg>/Wtsi	N	MGI:5576271
MGI:6261981	M	MP:0002152	abnormal brain morphology	Bhlha9<tm1.1(KOMP)Vlcg>/Bhlha9<tm1.1(KOMP)Vlcg>	C57BL/6N-Bhlha9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261981	M	MP:0001891	hydrocephaly	Bhlha9<tm1.1(KOMP)Vlcg>/Bhlha9<tm1.1(KOMP)Vlcg>	C57BL/6N-Bhlha9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6261982	M	MP:0005565	increased blood urea nitrogen level	Bhlhe40<tm1b(KOMP)Wtsi>/Bhlhe40<tm1b(KOMP)Wtsi>	C57BL/6N-Bhlhe40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261982	F	MP:0008810	increased circulating iron level	Bhlhe40<tm1b(KOMP)Wtsi>/Bhlhe40<tm1b(KOMP)Wtsi>	C57BL/6N-Bhlhe40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261982	M	MP:0005561	increased mean corpuscular hemoglobin	Bhlhe40<tm1b(KOMP)Wtsi>/Bhlhe40<tm1b(KOMP)Wtsi>	C57BL/6N-Bhlhe40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261982	M	MP:0005179	decreased circulating cholesterol level	Bhlhe40<tm1b(KOMP)Wtsi>/Bhlhe40<tm1b(KOMP)Wtsi>	C57BL/6N-Bhlhe40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261982	M	MP:0003019	increased circulating chloride level	Bhlhe40<tm1b(KOMP)Wtsi>/Bhlhe40<tm1b(KOMP)Wtsi>	C57BL/6N-Bhlhe40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261982	F	MP:0010087	increased circulating fructosamine level	Bhlhe40<tm1b(KOMP)Wtsi>/Bhlhe40<tm1b(KOMP)Wtsi>	C57BL/6N-Bhlhe40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261982	M	MP:0000186	decreased circulating HDL cholesterol level	Bhlhe40<tm1b(KOMP)Wtsi>/Bhlhe40<tm1b(KOMP)Wtsi>	C57BL/6N-Bhlhe40<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261983	F	MP:0005562	decreased mean corpuscular hemoglobin	Bin2<em1(IMPC)Wtsi>/Bin2<em1(IMPC)Wtsi>	C57BL/6N-Bin2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261983	M	MP:0003179	thrombocytopenia	Bin2<em1(IMPC)Wtsi>/Bin2<em1(IMPC)Wtsi>	C57BL/6N-Bin2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261984	M	MP:0005560	decreased circulating glucose level	Bivm<tm1b(KOMP)Wtsi>/Bivm<tm1b(KOMP)Wtsi>	C57BL/6N-Bivm<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6261987	M	MP:0011942	decreased fluid intake	Bnc2<tm1b(KOMP)Wtsi>/Bnc2<+>	C57BL/6N-Bnc2<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6261987	M	MP:0001417	decreased exploration in new environment	Bnc2<tm1b(KOMP)Wtsi>/Bnc2<+>	C57BL/6N-Bnc2<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6261989	F	MP:0002606	increased basophil cell number	Bod1<tm1b(KOMP)Wtsi>/Bod1<+>	C57BL/6N-Bod1<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6261989	M	MP:0002833	increased heart weight	Bod1<tm1b(KOMP)Wtsi>/Bod1<+>	C57BL/6N-Bod1<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6261989	F	MP:0005011	increased eosinophil cell number	Bod1<tm1b(KOMP)Wtsi>/Bod1<+>	C57BL/6N-Bod1<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6261991	F	MP:0000194	increased circulating calcium level	Borcs6<tm1.1(KOMP)Vlcg>/Borcs6<+>	B6N(Cg)-Borcs6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6261991	F	MP:0010024	increased total body fat amount	Borcs6<tm1.1(KOMP)Vlcg>/Borcs6<+>	B6N(Cg)-Borcs6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6261994	F	MP:0004924	abnormal behavior	Bpifa2<em1(IMPC)Mbp>/Bpifa2<em1(IMPC)Mbp>	C57BL/6NCrl-Bpifa2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261994	M	MP:0004931	enlarged epididymis	Bpifa2<em1(IMPC)Mbp>/Bpifa2<em1(IMPC)Mbp>	C57BL/6NCrl-Bpifa2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261994	M	MP:0002631	abnormal epididymis morphology	Bpifa2<em1(IMPC)Mbp>/Bpifa2<em1(IMPC)Mbp>	C57BL/6NCrl-Bpifa2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261994	F	MP:0001402	decreased locomotor activity	Bpifa2<em1(IMPC)Mbp>/Bpifa2<em1(IMPC)Mbp>	C57BL/6NCrl-Bpifa2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6261994	F	MP:0020870	decreased thigmotaxis	Bpifa2<em1(IMPC)Mbp>/Bpifa2<em1(IMPC)Mbp>	C57BL/6NCrl-Bpifa2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262000	M	MP:0001406	abnormal gait	Brip1<em1(IMPC)J>/Brip1<em1(IMPC)J>	C57BL/6NJ-Brip1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262000	F	MP:0001399	hyperactivity	Brip1<em1(IMPC)J>/Brip1<em1(IMPC)J>	C57BL/6NJ-Brip1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262000	F	MP:0002590	increased mean corpuscular volume	Brip1<em1(IMPC)J>/Brip1<em1(IMPC)J>	C57BL/6NJ-Brip1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262000	F	MP:0002968	increased circulating alkaline phosphatase level	Brip1<em1(IMPC)J>/Brip1<em1(IMPC)J>	C57BL/6NJ-Brip1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262000	F	MP:0003179	thrombocytopenia	Brip1<em1(IMPC)J>/Brip1<em1(IMPC)J>	C57BL/6NJ-Brip1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262000	F	MP:0002075	abnormal coat/hair pigmentation	Brip1<em1(IMPC)J>/Brip1<em1(IMPC)J>	C57BL/6NJ-Brip1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262000	M	MP:0010053	decreased grip strength	Brip1<em1(IMPC)J>/Brip1<em1(IMPC)J>	C57BL/6NJ-Brip1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262000	F	MP:0001304	cataract	Brip1<em1(IMPC)J>/Brip1<em1(IMPC)J>	C57BL/6NJ-Brip1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262002	M	MP:0001925	male infertility	Brwd1<em1(IMPC)Tcp>/Brwd1<em1(IMPC)Tcp>	C57BL/6NCrl-Brwd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262002	M	MP:0002059	abnormal seminal vesicle morphology	Brwd1<em1(IMPC)Tcp>/Brwd1<em1(IMPC)Tcp>	C57BL/6NCrl-Brwd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262002	F	MP:0001926	female infertility	Brwd1<em1(IMPC)Tcp>/Brwd1<em1(IMPC)Tcp>	C57BL/6NCrl-Brwd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262002	F	MP:0000689	abnormal spleen morphology	Brwd1<em1(IMPC)Tcp>/Brwd1<em1(IMPC)Tcp>	C57BL/6NCrl-Brwd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262002	M	MP:0001147	small testis	Brwd1<em1(IMPC)Tcp>/Brwd1<em1(IMPC)Tcp>	C57BL/6NCrl-Brwd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262003	F	MP:0009142	decreased prepulse inhibition	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262003	M	MP:0005343	increased circulating aspartate transaminase level	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262003	F	MP:0003795	abnormal bone structure	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262003	F	MP:0000220	increased monocyte cell number	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262003	M	MP:0011939	increased food intake	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262003	F	MP:0005292	improved glucose tolerance	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262003	M	MP:0010379	decreased respiratory quotient	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262003	F	MP:0001258	decreased body length	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262003	M	MP:0001402	decreased locomotor activity	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262003	F	MP:0010124	decreased bone mineral content	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262003	M	MP:0005559	increased circulating glucose level	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262003	M	MP:0011941	increased fluid intake	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262003	F	MP:0011962	increased cornea thickness	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262003	F	MP:0010025	decreased total body fat amount	Bscl2<tm1b(EUCOMM)Hmgu>/Bscl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Bscl2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262004	M	MP:0004931	enlarged epididymis	Btbd17<em1(IMPC)Mbp>/Btbd17<em1(IMPC)Mbp>	C57BL/6NCrl-Btbd17<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262004	F	MP:0001120	abnormal uterus morphology	Btbd17<em1(IMPC)Mbp>/Btbd17<em1(IMPC)Mbp>	C57BL/6NCrl-Btbd17<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262004	F	MP:0001944	abnormal pancreas morphology	Btbd17<em1(IMPC)Mbp>/Btbd17<em1(IMPC)Mbp>	C57BL/6NCrl-Btbd17<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262004	F	MP:0000703	abnormal thymus morphology	Btbd17<em1(IMPC)Mbp>/Btbd17<em1(IMPC)Mbp>	C57BL/6NCrl-Btbd17<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262004	F	MP:0001126	abnormal ovary morphology	Btbd17<em1(IMPC)Mbp>/Btbd17<em1(IMPC)Mbp>	C57BL/6NCrl-Btbd17<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262004	F	MP:0004906	enlarged uterus	Btbd17<em1(IMPC)Mbp>/Btbd17<em1(IMPC)Mbp>	C57BL/6NCrl-Btbd17<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262004	F	MP:0002135	abnormal kidney morphology	Btbd17<em1(IMPC)Mbp>/Btbd17<em1(IMPC)Mbp>	C57BL/6NCrl-Btbd17<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262004	F	MP:0008528	polycystic kidney	Btbd17<em1(IMPC)Mbp>/Btbd17<em1(IMPC)Mbp>	C57BL/6NCrl-Btbd17<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262004	F	MP:0000691	enlarged spleen	Btbd17<em1(IMPC)Mbp>/Btbd17<em1(IMPC)Mbp>	C57BL/6NCrl-Btbd17<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262004	M	MP:0002631	abnormal epididymis morphology	Btbd17<em1(IMPC)Mbp>/Btbd17<em1(IMPC)Mbp>	C57BL/6NCrl-Btbd17<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262006	F	MP:0005560	decreased circulating glucose level	Bud23<em2(IMPC)H>/Bud23<+>	C57BL/6N-Bud23<em2(IMPC)H>/H	N	MGI:5576271
MGI:6262008	F	MP:0001304	cataract	Bzw1<em1(IMPC)J>/Bzw1<em1(IMPC)J>	C57BL/6NJ-Bzw1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262008	M	MP:0001925	male infertility	Bzw1<em1(IMPC)J>/Bzw1<em1(IMPC)J>	C57BL/6NJ-Bzw1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262009	F	MP:0010053	decreased grip strength	C1qc<em1(IMPC)J>/C1qc<em1(IMPC)J>	C57BL/6NJ-C1qc<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262009	F	MP:0002941	increased circulating alanine transaminase level	C1qc<em1(IMPC)J>/C1qc<em1(IMPC)J>	C57BL/6NJ-C1qc<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262009	F	MP:0005343	increased circulating aspartate transaminase level	C1qc<em1(IMPC)J>/C1qc<em1(IMPC)J>	C57BL/6NJ-C1qc<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262009	F	MP:0000194	increased circulating calcium level	C1qc<em1(IMPC)J>/C1qc<em1(IMPC)J>	C57BL/6NJ-C1qc<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262009	F	MP:0000572	abnormal autopod morphology	C1qc<em1(IMPC)J>/C1qc<em1(IMPC)J>	C57BL/6NJ-C1qc<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262010	M	MP:0002599	increased mean platelet volume	C2cd4a<em1(IMPC)H>/C2cd4a<em1(IMPC)H>	C57BL/6NTac-C2cd4a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262011	M	MP:0000186	decreased circulating HDL cholesterol level	C2cd4b<em1(IMPC)Wtsi>/C2cd4b<em1(IMPC)Wtsi>	C57BL/6N-C2cd4b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262011	M	MP:0002599	increased mean platelet volume	C2cd4b<em1(IMPC)Wtsi>/C2cd4b<em1(IMPC)Wtsi>	C57BL/6N-C2cd4b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262011	M	MP:0005179	decreased circulating cholesterol level	C2cd4b<em1(IMPC)Wtsi>/C2cd4b<em1(IMPC)Wtsi>	C57BL/6N-C2cd4b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262011	M	MP:0010067	increased red blood cell distribution width	C2cd4b<em1(IMPC)Wtsi>/C2cd4b<em1(IMPC)Wtsi>	C57BL/6N-C2cd4b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262011	M	MP:0002874	decreased hemoglobin content	C2cd4b<em1(IMPC)Wtsi>/C2cd4b<em1(IMPC)Wtsi>	C57BL/6N-C2cd4b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262011	M	MP:0002644	decreased circulating triglyceride level	C2cd4b<em1(IMPC)Wtsi>/C2cd4b<em1(IMPC)Wtsi>	C57BL/6N-C2cd4b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262012	M	MP:0008528	polycystic kidney	C3ar1<tm1.1(KOMP)Vlcg>/C3ar1<tm1.1(KOMP)Vlcg>	C57BL/6N-C3ar1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262012	M	MP:0002135	abnormal kidney morphology	C3ar1<tm1.1(KOMP)Vlcg>/C3ar1<tm1.1(KOMP)Vlcg>	C57BL/6N-C3ar1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262013	M	MP:0000367	abnormal coat/ hair morphology	Cracd<em1(IMPC)J>/Cracd<em1(IMPC)J>	C57BL/6NJ-Cracd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262014	F	MP:0001399	hyperactivity	C7<em1(IMPC)J>/C7<em1(IMPC)J>	C57BL/6NJ-C7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262014	M	MP:0000432	abnormal head morphology	C7<em1(IMPC)J>/C7<em1(IMPC)J>	C57BL/6NJ-C7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262014	F	MP:0000367	abnormal coat/ hair morphology	C7<em1(IMPC)J>/C7<em1(IMPC)J>	C57BL/6NJ-C7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262014	F	MP:0001415	increased exploration in new environment	C7<em1(IMPC)J>/C7<em1(IMPC)J>	C57BL/6NJ-C7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262015	M	MP:0001417	decreased exploration in new environment	C8a<tm1b(EUCOMM)Hmgu>/C8a<tm1b(EUCOMM)Hmgu>	C57BL/6N-C8a<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:6262015	M	MP:0005013	increased lymphocyte cell number	C8a<tm1b(EUCOMM)Hmgu>/C8a<tm1b(EUCOMM)Hmgu>	C57BL/6N-C8a<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:6262015	M	MP:0000062	increased bone mineral density	C8a<tm1b(EUCOMM)Hmgu>/C8a<tm1b(EUCOMM)Hmgu>	C57BL/6N-C8a<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:6262016	M	MP:0010068	decreased red blood cell distribution width	C8b<tm1b(EUCOMM)Hmgu>/C8b<tm1b(EUCOMM)Hmgu>	C57BL/6N-C8b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262019	M	MP:0002092	abnormal eye morphology	Cacna1f<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Cacna1f<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262019	M	MP:0005553	increased circulating creatinine level	Cacna1f<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Cacna1f<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262020	M	MP:0000538	abnormal urinary bladder morphology	Cacnb2<tm1.1(KOMP)Vlcg>/Cacnb2<tm1.1(KOMP)Vlcg>	C57BL/6N-Cacnb2<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262020	M	MP:0005559	increased circulating glucose level	Cacnb2<tm1.1(KOMP)Vlcg>/Cacnb2<tm1.1(KOMP)Vlcg>	C57BL/6N-Cacnb2<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262020	F	MP:0000266	abnormal heart morphology	Cacnb2<tm1.1(KOMP)Vlcg>/Cacnb2<tm1.1(KOMP)Vlcg>	C57BL/6N-Cacnb2<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262020	F	MP:0000274	enlarged heart	Cacnb2<tm1.1(KOMP)Vlcg>/Cacnb2<tm1.1(KOMP)Vlcg>	C57BL/6N-Cacnb2<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262022	M	MP:0000274	enlarged heart	Calcb<tm1.1(KOMP)Vlcg>/Calcb<tm1.1(KOMP)Vlcg>	C57BL/6N-Calcb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262022	F	MP:0000955	abnormal spinal cord morphology	Calcb<tm1.1(KOMP)Vlcg>/Calcb<tm1.1(KOMP)Vlcg>	C57BL/6N-Calcb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262022	M	MP:0001944	abnormal pancreas morphology	Calcb<tm1.1(KOMP)Vlcg>/Calcb<tm1.1(KOMP)Vlcg>	C57BL/6N-Calcb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262022	M	MP:0002631	abnormal epididymis morphology	Calcb<tm1.1(KOMP)Vlcg>/Calcb<tm1.1(KOMP)Vlcg>	C57BL/6N-Calcb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262022	M	MP:0000266	abnormal heart morphology	Calcb<tm1.1(KOMP)Vlcg>/Calcb<tm1.1(KOMP)Vlcg>	C57BL/6N-Calcb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262022	M	MP:0002135	abnormal kidney morphology	Calcb<tm1.1(KOMP)Vlcg>/Calcb<tm1.1(KOMP)Vlcg>	C57BL/6N-Calcb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262022	M	MP:0004931	enlarged epididymis	Calcb<tm1.1(KOMP)Vlcg>/Calcb<tm1.1(KOMP)Vlcg>	C57BL/6N-Calcb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262024	M	MP:0001289	persistence of hyaloid vascular system	Calhm2<tm1b(KOMP)Mbp>/Calhm2<tm1b(KOMP)Mbp>	C57BL/6N-Calhm2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6262024	M	MP:0001944	abnormal pancreas morphology	Calhm2<tm1b(KOMP)Mbp>/Calhm2<tm1b(KOMP)Mbp>	C57BL/6N-Calhm2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6262024	M	MP:0003450	enlarged pancreas	Calhm2<tm1b(KOMP)Mbp>/Calhm2<tm1b(KOMP)Mbp>	C57BL/6N-Calhm2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6262025	M	MP:0010024	increased total body fat amount	Camk1d<em1(IMPC)Mbp>/Camk1d<em1(IMPC)Mbp>	C57BL/6NCrl-Camk1d<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262025	M	MP:0003961	decreased lean body mass	Camk1d<em1(IMPC)Mbp>/Camk1d<em1(IMPC)Mbp>	C57BL/6NCrl-Camk1d<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262025	M	MP:0002834	decreased heart weight	Camk1d<em1(IMPC)Mbp>/Camk1d<em1(IMPC)Mbp>	C57BL/6NCrl-Camk1d<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262025	F	MP:0002092	abnormal eye morphology	Camk1d<em1(IMPC)Mbp>/Camk1d<em1(IMPC)Mbp>	C57BL/6NCrl-Camk1d<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262025	F	MP:0010052	increased grip strength	Camk1d<em1(IMPC)Mbp>/Camk1d<em1(IMPC)Mbp>	C57BL/6NCrl-Camk1d<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262025	M	MP:0000598	abnormal liver morphology	Camk1d<em1(IMPC)Mbp>/Camk1d<em1(IMPC)Mbp>	C57BL/6NCrl-Camk1d<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262025	M	MP:0000063	decreased bone mineral density	Camk1d<em1(IMPC)Mbp>/Camk1d<em1(IMPC)Mbp>	C57BL/6NCrl-Camk1d<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262025	F	MP:0003450	enlarged pancreas	Camk1d<em1(IMPC)Mbp>/Camk1d<em1(IMPC)Mbp>	C57BL/6NCrl-Camk1d<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262026	M	MP:0005292	improved glucose tolerance	Camk2b<tm1b(EUCOMM)Hmgu>/Camk2b<+>	C57BL/6N-Camk2b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262026	M	MP:0001364	decreased anxiety-related response	Camk2b<tm1b(EUCOMM)Hmgu>/Camk2b<+>	C57BL/6N-Camk2b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262026	F	MP:0009142	decreased prepulse inhibition	Camk2b<tm1b(EUCOMM)Hmgu>/Camk2b<+>	C57BL/6N-Camk2b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262028	M	MP:0000186	decreased circulating HDL cholesterol level	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<+>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262028	M	MP:0002874	decreased hemoglobin content	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<+>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262028	M	MP:0005179	decreased circulating cholesterol level	Camsap3<tm1a(EUCOMM)Wtsi>/Camsap3<+>	C57BL/6N-Camsap3<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262030	F	MP:0005084	abnormal gallbladder morphology	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	F	MP:0000689	abnormal spleen morphology	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	F	MP:0002339	abnormal lymph node morphology	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	M	MP:0005333	decreased heart rate	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	M	MP:0003642	absent seminal vesicle	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	F	MP:0001126	abnormal ovary morphology	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	F	MP:0001120	abnormal uterus morphology	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	F	MP:0002188	small heart	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	M	MP:0002997	enlarged seminal vesicle	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	F	MP:0000691	enlarged spleen	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	F	MP:0002989	small kidney	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	F	MP:0000266	abnormal heart morphology	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	F	MP:0009342	enlarged gallbladder	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	F	MP:0000274	enlarged heart	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	F	MP:0002060	abnormal skin morphology	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	F	MP:0000702	enlarged lymph nodes	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	M	MP:0013279	increased fasting circulating glucose level	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262030	F	MP:0002135	abnormal kidney morphology	Cand1<em1(IMPC)Mbp>/Cand1<+>	C57BL/6NCrl-Cand1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262031	M	MP:0008806	increased circulating amylase level	Capn12<tm1b(EUCOMM)Hmgu>/Capn12<tm1b(EUCOMM)Hmgu>	C57BL/6N-Capn12<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262031	M	MP:0005559	increased circulating glucose level	Capn12<tm1b(EUCOMM)Hmgu>/Capn12<tm1b(EUCOMM)Hmgu>	C57BL/6N-Capn12<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262031	M	MP:0001304	cataract	Capn12<tm1b(EUCOMM)Hmgu>/Capn12<tm1b(EUCOMM)Hmgu>	C57BL/6N-Capn12<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262031	M	MP:0011886	increased circulating lipase level	Capn12<tm1b(EUCOMM)Hmgu>/Capn12<tm1b(EUCOMM)Hmgu>	C57BL/6N-Capn12<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262031	M	MP:0001417	decreased exploration in new environment	Capn12<tm1b(EUCOMM)Hmgu>/Capn12<tm1b(EUCOMM)Hmgu>	C57BL/6N-Capn12<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262034	F	MP:0009142	decreased prepulse inhibition	Caskin1<em1(IMPC)Mbp>/Caskin1<em1(IMPC)Mbp>	C57BL/6NCrl-Caskin1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262034	M	MP:0001402	decreased locomotor activity	Caskin1<em1(IMPC)Mbp>/Caskin1<em1(IMPC)Mbp>	C57BL/6NCrl-Caskin1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262035	M	MP:0010088	decreased circulating fructosamine level	Cbr2<tm1b(EUCOMM)Hmgu>/Cbr2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cbr2<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6262035	M	MP:0008805	decreased circulating amylase level	Cbr2<tm1b(EUCOMM)Hmgu>/Cbr2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cbr2<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6262039	M	MP:0005293	impaired glucose tolerance	Ccdc116<tm1.1(KOMP)Vlcg>/Ccdc116<tm1.1(KOMP)Vlcg>	C57BL/6N-Ccdc116<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262041	F	MP:0001402	decreased locomotor activity	Ccdc141<tm1.1(KOMP)Wtsi>/Ccdc141<tm1.1(KOMP)Wtsi>	C57BL/6N-Ccdc141<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262043	M	MP:0005293	impaired glucose tolerance	Odad3<tm1b(EUCOMM)Hmgu>/Odad3<+>	C57BL/6N-Odad3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262043	F	MP:0003795	abnormal bone structure	Odad3<tm1b(EUCOMM)Hmgu>/Odad3<+>	C57BL/6N-Odad3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262044	M	MP:0001925	male infertility	Cfap119<tm1b(EUCOMM)Hmgu>/Cfap119<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cfap119<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262044	M	MP:0005178	increased circulating cholesterol level	Cfap119<tm1b(EUCOMM)Hmgu>/Cfap119<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cfap119<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262044	F	MP:0001402	decreased locomotor activity	Cfap119<tm1b(EUCOMM)Hmgu>/Cfap119<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cfap119<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262044	M	MP:0001556	increased circulating HDL cholesterol level	Cfap119<tm1b(EUCOMM)Hmgu>/Cfap119<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cfap119<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262045	F	MP:0005633	increased circulating sodium level	Ccdc18<tm1a(EUCOMM)Wtsi>/Ccdc18<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ccdc18<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262045	M	MP:0001552	increased circulating triglyceride level	Ccdc18<tm1a(EUCOMM)Wtsi>/Ccdc18<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ccdc18<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262045	F	MP:0005568	increased circulating total protein level	Ccdc18<tm1a(EUCOMM)Wtsi>/Ccdc18<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ccdc18<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262045	F	MP:0003443	increased circulating glycerol level	Ccdc18<tm1a(EUCOMM)Wtsi>/Ccdc18<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ccdc18<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262045	F	MP:0002968	increased circulating alkaline phosphatase level	Ccdc18<tm1a(EUCOMM)Wtsi>/Ccdc18<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ccdc18<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262046	F	MP:0001513	limb grasping	Ccdc28a<tm3b(EUCOMM)Wtsi>/Ccdc28a<tm3b(EUCOMM)Wtsi>	B6N(Cg)-Ccdc28a<tm3b(EUCOMM)Wtsi>/2J	N	MGI:5576271
MGI:6262046	F	MP:0002757	decreased vertical activity	Ccdc28a<tm3b(EUCOMM)Wtsi>/Ccdc28a<tm3b(EUCOMM)Wtsi>	B6N(Cg)-Ccdc28a<tm3b(EUCOMM)Wtsi>/2J	N	MGI:5576271
MGI:6262046	F	MP:0001399	hyperactivity	Ccdc28a<tm3b(EUCOMM)Wtsi>/Ccdc28a<tm3b(EUCOMM)Wtsi>	B6N(Cg)-Ccdc28a<tm3b(EUCOMM)Wtsi>/2J	N	MGI:5576271
MGI:6262046	M	MP:0001925	male infertility	Ccdc28a<tm3b(EUCOMM)Wtsi>/Ccdc28a<tm3b(EUCOMM)Wtsi>	B6N(Cg)-Ccdc28a<tm3b(EUCOMM)Wtsi>/2J	N	MGI:5576271
MGI:6262046	M	MP:0005333	decreased heart rate	Ccdc28a<tm3b(EUCOMM)Wtsi>/Ccdc28a<tm3b(EUCOMM)Wtsi>	B6N(Cg)-Ccdc28a<tm3b(EUCOMM)Wtsi>/2J	N	MGI:5576271
MGI:6262046	F	MP:0005102	abnormal iris pigmentation	Ccdc28a<tm3b(EUCOMM)Wtsi>/Ccdc28a<tm3b(EUCOMM)Wtsi>	B6N(Cg)-Ccdc28a<tm3b(EUCOMM)Wtsi>/2J	N	MGI:5576271
MGI:6262046	F	MP:0001364	decreased anxiety-related response	Ccdc28a<tm3b(EUCOMM)Wtsi>/Ccdc28a<tm3b(EUCOMM)Wtsi>	B6N(Cg)-Ccdc28a<tm3b(EUCOMM)Wtsi>/2J	N	MGI:5576271
MGI:6262046	M	MP:0010506	prolonged RR interval	Ccdc28a<tm3b(EUCOMM)Wtsi>/Ccdc28a<tm3b(EUCOMM)Wtsi>	B6N(Cg)-Ccdc28a<tm3b(EUCOMM)Wtsi>/2J	N	MGI:5576271
MGI:6262046	F	MP:0010052	increased grip strength	Ccdc28a<tm3b(EUCOMM)Wtsi>/Ccdc28a<tm3b(EUCOMM)Wtsi>	B6N(Cg)-Ccdc28a<tm3b(EUCOMM)Wtsi>/2J	N	MGI:5576271
MGI:6262047	M	MP:0009142	decreased prepulse inhibition	Ccdc30<em1(IMPC)J>/Ccdc30<em1(IMPC)J>	C57BL/6NJ-Ccdc30<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262048	M	MP:0002591	decreased mean corpuscular volume	Ccdc59<em1(IMPC)J>/Ccdc59<+>	C57BL/6NJ-Ccdc59<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262050	F	MP:0009709	hydrometra	Ccdc65<em1(IMPC)Mbp>/Ccdc65<+>	C57BL/6NCrl-Ccdc65<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262054	M	MP:0010024	increased total body fat amount	Ccdc8<em1(IMPC)Tcp>/Ccdc8<+>	C57BL/6NCrl-Ccdc8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262056	F	MP:0001417	decreased exploration in new environment	Ccdc9b<em1(IMPC)Tcp>/Ccdc9b<em1(IMPC)Tcp>	C57BL/6NCrl-Ccdc9b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262056	F	MP:0009142	decreased prepulse inhibition	Ccdc9b<em1(IMPC)Tcp>/Ccdc9b<em1(IMPC)Tcp>	C57BL/6NCrl-Ccdc9b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262057	M	MP:0001925	male infertility	Ccnb1ip1<em1(IMPC)Tcp>/Ccnb1ip1<em1(IMPC)Tcp>	C57BL/6NCrl-Ccnb1ip1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262057	F	MP:0001926	female infertility	Ccnb1ip1<em1(IMPC)Tcp>/Ccnb1ip1<em1(IMPC)Tcp>	C57BL/6NCrl-Ccnb1ip1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262057	M	MP:0000702	enlarged lymph nodes	Ccnb1ip1<em1(IMPC)Tcp>/Ccnb1ip1<em1(IMPC)Tcp>	C57BL/6NCrl-Ccnb1ip1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262058	M	MP:0013279	increased fasting circulating glucose level	Ccnd2<tm1b(KOMP)Mbp>/Ccnd2<tm1b(KOMP)Mbp>	C57BL/6N-Ccnd2<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6262058	M	MP:0001147	small testis	Ccnd2<tm1b(KOMP)Mbp>/Ccnd2<tm1b(KOMP)Mbp>	C57BL/6N-Ccnd2<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6262058	F	MP:0010123	increased bone mineral content	Ccnd2<tm1b(KOMP)Mbp>/Ccnd2<tm1b(KOMP)Mbp>	C57BL/6N-Ccnd2<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6262058	F	MP:0001512	trunk curl	Ccnd2<tm1b(KOMP)Mbp>/Ccnd2<tm1b(KOMP)Mbp>	C57BL/6N-Ccnd2<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6262058	F	MP:0008810	increased circulating iron level	Ccnd2<tm1b(KOMP)Mbp>/Ccnd2<tm1b(KOMP)Mbp>	C57BL/6N-Ccnd2<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6262058	F	MP:0002968	increased circulating alkaline phosphatase level	Ccnd2<tm1b(KOMP)Mbp>/Ccnd2<tm1b(KOMP)Mbp>	C57BL/6N-Ccnd2<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6262058	M	MP:0000438	abnormal cranium morphology	Ccnd2<tm1b(KOMP)Mbp>/Ccnd2<tm1b(KOMP)Mbp>	C57BL/6N-Ccnd2<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6262058	M	MP:0001399	hyperactivity	Ccnd2<tm1b(KOMP)Mbp>/Ccnd2<tm1b(KOMP)Mbp>	C57BL/6N-Ccnd2<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6262058	M	MP:0004174	abnormal spine curvature	Ccnd2<tm1b(KOMP)Mbp>/Ccnd2<tm1b(KOMP)Mbp>	C57BL/6N-Ccnd2<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6262059	M	MP:0001552	increased circulating triglyceride level	Ccnq<tm1.1(KOMP)Vlcg>/Ccnq<+>	C57BL/6N-Ccnq<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262062	M	MP:0000689	abnormal spleen morphology	Ccr6<tm1.1(KOMP)Vlcg>/Ccr6<tm1.1(KOMP)Vlcg>	C57BL/6N-Ccr6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262062	F	MP:0001399	hyperactivity	Ccr6<tm1.1(KOMP)Vlcg>/Ccr6<tm1.1(KOMP)Vlcg>	C57BL/6N-Ccr6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262062	M	MP:0005333	decreased heart rate	Ccr6<tm1.1(KOMP)Vlcg>/Ccr6<tm1.1(KOMP)Vlcg>	C57BL/6N-Ccr6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262062	M	MP:0010506	prolonged RR interval	Ccr6<tm1.1(KOMP)Vlcg>/Ccr6<tm1.1(KOMP)Vlcg>	C57BL/6N-Ccr6<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262064	M	MP:0001284	absent vibrissae	Cd109<tm1.1(KOMP)Vlcg>/Cd109<tm1.1(KOMP)Vlcg>	C57BL/6N-Cd109<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262066	M	MP:0005178	increased circulating cholesterol level	Cd22<tm1b(EUCOMM)Wtsi>/Cd22<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cd22<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262066	M	MP:0000220	increased monocyte cell number	Cd22<tm1b(EUCOMM)Wtsi>/Cd22<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cd22<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262066	F	MP:0009709	hydrometra	Cd22<tm1b(EUCOMM)Wtsi>/Cd22<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cd22<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262066	F	MP:0001102	small superior vagus ganglion	Cd22<tm1b(EUCOMM)Wtsi>/Cd22<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cd22<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262067	M	MP:0002060	abnormal skin morphology	Cd248<tm1.1(KOMP)Vlcg>/Cd248<tm1.1(KOMP)Vlcg>	C57BL/6N-Cd248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262067	M	MP:0001146	abnormal testis morphology	Cd248<tm1.1(KOMP)Vlcg>/Cd248<tm1.1(KOMP)Vlcg>	C57BL/6N-Cd248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262067	M	MP:0001258	decreased body length	Cd248<tm1.1(KOMP)Vlcg>/Cd248<tm1.1(KOMP)Vlcg>	C57BL/6N-Cd248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262067	M	MP:0002079	increased circulating insulin level	Cd248<tm1.1(KOMP)Vlcg>/Cd248<tm1.1(KOMP)Vlcg>	C57BL/6N-Cd248<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262068	M	MP:0001399	hyperactivity	Cd276<tm2b(EUCOMM)Hmgu>/Cd276<tm2b(EUCOMM)Hmgu>	C57BL/6N-Cd276<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6262069	M	MP:0002599	increased mean platelet volume	Cd300a<tm1b(EUCOMM)Hmgu>/Cd300a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cd300a<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262069	F	MP:0010052	increased grip strength	Cd300a<tm1b(EUCOMM)Hmgu>/Cd300a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cd300a<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262069	F	MP:0001325	abnormal retina morphology	Cd300a<tm1b(EUCOMM)Hmgu>/Cd300a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cd300a<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262069	M	MP:0001406	abnormal gait	Cd300a<tm1b(EUCOMM)Hmgu>/Cd300a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cd300a<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262070	M	MP:0001258	decreased body length	Cd300c<em1(IMPC)Wtsi>/Cd300c<em1(IMPC)Wtsi>	C57BL/6N-Cd300c<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:6262070	M	MP:0000218	increased leukocyte cell number	Cd300c<em1(IMPC)Wtsi>/Cd300c<em1(IMPC)Wtsi>	C57BL/6N-Cd300c<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:6262071	F	MP:0002941	increased circulating alanine transaminase level	Cd300ld2<em1(IMPC)Wtsi>/Cd300ld2<em1(IMPC)Wtsi>	C57BL/6N-Cd300ld2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262071	M	MP:0003960	increased lean body mass	Cd300ld2<em1(IMPC)Wtsi>/Cd300ld2<em1(IMPC)Wtsi>	C57BL/6N-Cd300ld2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262071	F	MP:0005343	increased circulating aspartate transaminase level	Cd300ld2<em1(IMPC)Wtsi>/Cd300ld2<em1(IMPC)Wtsi>	C57BL/6N-Cd300ld2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262071	F	MP:0010090	increased circulating creatine kinase level	Cd300ld2<em1(IMPC)Wtsi>/Cd300ld2<em1(IMPC)Wtsi>	C57BL/6N-Cd300ld2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262072	F	MP:0013279	increased fasting circulating glucose level	Cd33<tm1.1(KOMP)Vlcg>/Cd33<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cd33<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262074	M	MP:0001303	abnormal lens morphology	Cd7<tm1b(KOMP)Wtsi>/Cd7<tm1b(KOMP)Wtsi>	C57BL/6N-Cd7<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6262074	M	MP:0001304	cataract	Cd7<tm1b(KOMP)Wtsi>/Cd7<tm1b(KOMP)Wtsi>	C57BL/6N-Cd7<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6262075	M	MP:0000274	enlarged heart	Cdan1<tm1b(KOMP)Wtsi>/Cdan1<+>	C57BL/6N-Cdan1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262075	M	MP:0000266	abnormal heart morphology	Cdan1<tm1b(KOMP)Wtsi>/Cdan1<+>	C57BL/6N-Cdan1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262075	F	MP:0002941	increased circulating alanine transaminase level	Cdan1<tm1b(KOMP)Wtsi>/Cdan1<+>	C57BL/6N-Cdan1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262075	M	MP:0003179	thrombocytopenia	Cdan1<tm1b(KOMP)Wtsi>/Cdan1<+>	C57BL/6N-Cdan1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262075	M	MP:0001146	abnormal testis morphology	Cdan1<tm1b(KOMP)Wtsi>/Cdan1<+>	C57BL/6N-Cdan1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262075	M	MP:0001147	small testis	Cdan1<tm1b(KOMP)Wtsi>/Cdan1<+>	C57BL/6N-Cdan1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262077	M	MP:0000063	decreased bone mineral density	Cdc37l1<em1(IMPC)J>/Cdc37l1<em1(IMPC)J>	C57BL/6NJ-Cdc37l1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262077	F	MP:0001304	cataract	Cdc37l1<em1(IMPC)J>/Cdc37l1<em1(IMPC)J>	C57BL/6NJ-Cdc37l1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262078	F	MP:0001697	abnormal embryo size	Cdc42bpb<em1(IMPC)J>/Cdc42bpb<em1(IMPC)J>	C57BL/6NJ-Cdc42bpb<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262079	M	MP:0005343	increased circulating aspartate transaminase level	Cdc42ep3<em1(IMPC)Mbp>/Cdc42ep3<em1(IMPC)Mbp>	C57BL/6NCrl-Cdc42ep3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262079	M	MP:0020870	decreased thigmotaxis	Cdc42ep3<em1(IMPC)Mbp>/Cdc42ep3<em1(IMPC)Mbp>	C57BL/6NCrl-Cdc42ep3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262080	F	MP:0002075	abnormal coat/hair pigmentation	Cdc42ep5<tm1(KOMP)Wtsi>/Cdc42ep5<tm1(KOMP)Wtsi>	C57BL/6N-Cdc42ep5<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262080	M	MP:0003961	decreased lean body mass	Cdc42ep5<tm1(KOMP)Wtsi>/Cdc42ep5<tm1(KOMP)Wtsi>	C57BL/6N-Cdc42ep5<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262081	M	MP:0005419	decreased circulating serum albumin level	Cdc42<tm1b(EUCOMM)Hmgu>/Cdc42<+>	C57BL/6N-Cdc42<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262081	F	MP:0005178	increased circulating cholesterol level	Cdc42<tm1b(EUCOMM)Hmgu>/Cdc42<+>	C57BL/6N-Cdc42<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262081	M	MP:0000438	abnormal cranium morphology	Cdc42<tm1b(EUCOMM)Hmgu>/Cdc42<+>	C57BL/6N-Cdc42<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262081	F	MP:0002968	increased circulating alkaline phosphatase level	Cdc42<tm1b(EUCOMM)Hmgu>/Cdc42<+>	C57BL/6N-Cdc42<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262081	F	MP:0001556	increased circulating HDL cholesterol level	Cdc42<tm1b(EUCOMM)Hmgu>/Cdc42<+>	C57BL/6N-Cdc42<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262081	M	MP:0005343	increased circulating aspartate transaminase level	Cdc42<tm1b(EUCOMM)Hmgu>/Cdc42<+>	C57BL/6N-Cdc42<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262081	F	MP:0003068	enlarged kidney	Cdc42<tm1b(EUCOMM)Hmgu>/Cdc42<+>	C57BL/6N-Cdc42<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262083	F	MP:0002060	abnormal skin morphology	Cdc7<tm1.1(KOMP)Vlcg>/Cdc7<+>	C57BL/6N-Cdc7<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262083	M	MP:0000222	decreased neutrophil cell number	Cdc7<tm1.1(KOMP)Vlcg>/Cdc7<+>	C57BL/6N-Cdc7<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262084	M	MP:0009142	decreased prepulse inhibition	Cdca7l<em1(IMPC)Mbp>/Cdca7l<em1(IMPC)Mbp>	C57BL/6NCrl-Cdca7l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262084	F	MP:0002135	abnormal kidney morphology	Cdca7l<em1(IMPC)Mbp>/Cdca7l<em1(IMPC)Mbp>	C57BL/6NCrl-Cdca7l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262084	F	MP:0005178	increased circulating cholesterol level	Cdca7l<em1(IMPC)Mbp>/Cdca7l<em1(IMPC)Mbp>	C57BL/6NCrl-Cdca7l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262084	F	MP:0000702	enlarged lymph nodes	Cdca7l<em1(IMPC)Mbp>/Cdca7l<em1(IMPC)Mbp>	C57BL/6NCrl-Cdca7l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262084	M	MP:0002060	abnormal skin morphology	Cdca7l<em1(IMPC)Mbp>/Cdca7l<em1(IMPC)Mbp>	C57BL/6NCrl-Cdca7l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262084	F	MP:0000689	abnormal spleen morphology	Cdca7l<em1(IMPC)Mbp>/Cdca7l<em1(IMPC)Mbp>	C57BL/6NCrl-Cdca7l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262084	F	MP:0002339	abnormal lymph node morphology	Cdca7l<em1(IMPC)Mbp>/Cdca7l<em1(IMPC)Mbp>	C57BL/6NCrl-Cdca7l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262084	F	MP:0000691	enlarged spleen	Cdca7l<em1(IMPC)Mbp>/Cdca7l<em1(IMPC)Mbp>	C57BL/6NCrl-Cdca7l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262084	F	MP:0002989	small kidney	Cdca7l<em1(IMPC)Mbp>/Cdca7l<em1(IMPC)Mbp>	C57BL/6NCrl-Cdca7l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262085	F	MP:0000218	increased leukocyte cell number	Cdh10<tm2b(KOMP)Wtsi>/Cdh10<tm2b(KOMP)Wtsi>	C57BL/6N-Cdh10<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262085	F	MP:0000220	increased monocyte cell number	Cdh10<tm2b(KOMP)Wtsi>/Cdh10<tm2b(KOMP)Wtsi>	C57BL/6N-Cdh10<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262085	F	MP:0005013	increased lymphocyte cell number	Cdh10<tm2b(KOMP)Wtsi>/Cdh10<tm2b(KOMP)Wtsi>	C57BL/6N-Cdh10<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262085	M	MP:0003960	increased lean body mass	Cdh10<tm2b(KOMP)Wtsi>/Cdh10<tm2b(KOMP)Wtsi>	C57BL/6N-Cdh10<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262085	F	MP:0000219	increased neutrophil cell number	Cdh10<tm2b(KOMP)Wtsi>/Cdh10<tm2b(KOMP)Wtsi>	C57BL/6N-Cdh10<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262085	F	MP:0001297	microphthalmia	Cdh10<tm2b(KOMP)Wtsi>/Cdh10<tm2b(KOMP)Wtsi>	C57BL/6N-Cdh10<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262087	F	MP:0005561	increased mean corpuscular hemoglobin	Cdh23<tm2b(EUCOMM)Wtsi>/Cdh23<tm2b(EUCOMM)Wtsi>	C57BL/6N-Cdh23<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262087	M	MP:0010025	decreased total body fat amount	Cdh23<tm2b(EUCOMM)Wtsi>/Cdh23<tm2b(EUCOMM)Wtsi>	C57BL/6N-Cdh23<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262087	M	MP:0010123	increased bone mineral content	Cdh23<tm2b(EUCOMM)Wtsi>/Cdh23<tm2b(EUCOMM)Wtsi>	C57BL/6N-Cdh23<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262087	M	MP:0013278	decreased fasting circulating glucose level	Cdh23<tm2b(EUCOMM)Wtsi>/Cdh23<tm2b(EUCOMM)Wtsi>	C57BL/6N-Cdh23<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262087	F	MP:0001258	decreased body length	Cdh23<tm2b(EUCOMM)Wtsi>/Cdh23<tm2b(EUCOMM)Wtsi>	C57BL/6N-Cdh23<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262087	M	MP:0005560	decreased circulating glucose level	Cdh23<tm2b(EUCOMM)Wtsi>/Cdh23<tm2b(EUCOMM)Wtsi>	C57BL/6N-Cdh23<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262087	M	MP:0003960	increased lean body mass	Cdh23<tm2b(EUCOMM)Wtsi>/Cdh23<tm2b(EUCOMM)Wtsi>	C57BL/6N-Cdh23<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262087	M	MP:0000221	decreased leukocyte cell number	Cdh23<tm2b(EUCOMM)Wtsi>/Cdh23<tm2b(EUCOMM)Wtsi>	C57BL/6N-Cdh23<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262088	M	MP:0004924	abnormal behavior	Cdip1<tm1.1(KOMP)Vlcg>/Cdip1<+>	B6N(Cg)-Cdip1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262088	M	MP:0020870	decreased thigmotaxis	Cdip1<tm1.1(KOMP)Vlcg>/Cdip1<+>	B6N(Cg)-Cdip1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262089	M	MP:0000538	abnormal urinary bladder morphology	Cdk12<em1(IMPC)Tcp>/Cdk12<+>	C57BL/6NCrl-Cdk12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262089	F	MP:0001417	decreased exploration in new environment	Cdk12<em1(IMPC)Tcp>/Cdk12<+>	C57BL/6NCrl-Cdk12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262089	M	MP:0011874	enlarged urinary bladder	Cdk12<em1(IMPC)Tcp>/Cdk12<+>	C57BL/6NCrl-Cdk12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262089	F	MP:0000691	enlarged spleen	Cdk12<em1(IMPC)Tcp>/Cdk12<+>	C57BL/6NCrl-Cdk12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262089	M	MP:0000186	decreased circulating HDL cholesterol level	Cdk12<em1(IMPC)Tcp>/Cdk12<+>	C57BL/6NCrl-Cdk12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262089	F	MP:0000689	abnormal spleen morphology	Cdk12<em1(IMPC)Tcp>/Cdk12<+>	C57BL/6NCrl-Cdk12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262089	F	MP:0000598	abnormal liver morphology	Cdk12<em1(IMPC)Tcp>/Cdk12<+>	C57BL/6NCrl-Cdk12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262089	M	MP:0002875	decreased erythrocyte cell number	Cdk12<em1(IMPC)Tcp>/Cdk12<+>	C57BL/6NCrl-Cdk12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262089	M	MP:0002833	increased heart weight	Cdk12<em1(IMPC)Tcp>/Cdk12<+>	C57BL/6NCrl-Cdk12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262089	M	MP:0010067	increased red blood cell distribution width	Cdk12<em1(IMPC)Tcp>/Cdk12<+>	C57BL/6NCrl-Cdk12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262089	M	MP:0002874	decreased hemoglobin content	Cdk12<em1(IMPC)Tcp>/Cdk12<+>	C57BL/6NCrl-Cdk12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262089	M	MP:0000208	decreased hematocrit	Cdk12<em1(IMPC)Tcp>/Cdk12<+>	C57BL/6NCrl-Cdk12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262089	M	MP:0004952	increased spleen weight	Cdk12<em1(IMPC)Tcp>/Cdk12<+>	C57BL/6NCrl-Cdk12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262091	M	MP:0001488	increased startle reflex	Cdk13<tm1b(EUCOMM)Hmgu>/Cdk13<+>	C57BL/6N-Cdk13<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262093	M	MP:0010052	increased grip strength	Cdk19<em1(IMPC)J>/Cdk19<+>	C57BL/6NJ-Cdk19<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262094	M	MP:0001417	decreased exploration in new environment	Cdk5rap3<tm1b(EUCOMM)Hmgu>/Cdk5rap3<+>	C57BL/6N-Cdk5rap3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262094	M	MP:0013279	increased fasting circulating glucose level	Cdk5rap3<tm1b(EUCOMM)Hmgu>/Cdk5rap3<+>	C57BL/6N-Cdk5rap3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262094	M	MP:0011952	decreased cardiac stroke volume	Cdk5rap3<tm1b(EUCOMM)Hmgu>/Cdk5rap3<+>	C57BL/6N-Cdk5rap3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262095	F	MP:0001102	small superior vagus ganglion	Cdk6<tm1b(EUCOMM)Wtsi>/Cdk6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cdk6<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262095	M	MP:0002092	abnormal eye morphology	Cdk6<tm1b(EUCOMM)Wtsi>/Cdk6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cdk6<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262095	F	MP:0005561	increased mean corpuscular hemoglobin	Cdk6<tm1b(EUCOMM)Wtsi>/Cdk6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cdk6<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262102	M	MP:0010088	decreased circulating fructosamine level	Ceacam3<em1(IMPC)Wtsi>/Ceacam3<em1(IMPC)Wtsi>	C57BL/6N-Ceacam3<em1(IMPC)Wtsi>/WtsiCnrm	N	MGI:5576271
MGI:6262102	F	MP:0008806	increased circulating amylase level	Ceacam3<em1(IMPC)Wtsi>/Ceacam3<em1(IMPC)Wtsi>	C57BL/6N-Ceacam3<em1(IMPC)Wtsi>/WtsiCnrm	N	MGI:5576271
MGI:6262106	M	MP:0008797	facial cleft	Cep135<em1(IMPC)J>/Cep135<em1(IMPC)J>	C57BL/6NJ-Cep135<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262106	M	MP:0001297	microphthalmia	Cep135<em1(IMPC)J>/Cep135<em1(IMPC)J>	C57BL/6NJ-Cep135<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262106	F	MP:0000428	abnormal craniofacial morphology	Cep135<em1(IMPC)J>/Cep135<em1(IMPC)J>	C57BL/6NJ-Cep135<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262108	M	MP:0001925	male infertility	Cep250<tm1a(EUCOMM)Wtsi>/Cep250<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cep250<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262108	F	MP:0010024	increased total body fat amount	Cep250<tm1a(EUCOMM)Wtsi>/Cep250<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cep250<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262108	M	MP:0006358	absent pinna reflex	Cep250<tm1a(EUCOMM)Wtsi>/Cep250<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cep250<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262109	M	MP:0001925	male infertility	Cep41<tm1a(EUCOMM)Wtsi>/Cep41<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cep41<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262110	F	MP:0011100	preweaning lethality, complete penetrance	Cep55<em1(IMPC)Tcp>/Cep55<em1(IMPC)Tcp>	C57BL/6NCrl-Cep55<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262112	F	MP:0000266	abnormal heart morphology	Ces1d<em1(IMPC)Mbp>/Ces1d<em1(IMPC)Mbp>	C57BL/6NCrl-Ces1d<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262112	F	MP:0000274	enlarged heart	Ces1d<em1(IMPC)Mbp>/Ces1d<em1(IMPC)Mbp>	C57BL/6NCrl-Ces1d<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262112	F	MP:0008528	polycystic kidney	Ces1d<em1(IMPC)Mbp>/Ces1d<em1(IMPC)Mbp>	C57BL/6NCrl-Ces1d<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262112	F	MP:0005343	increased circulating aspartate transaminase level	Ces1d<em1(IMPC)Mbp>/Ces1d<em1(IMPC)Mbp>	C57BL/6NCrl-Ces1d<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262112	F	MP:0002135	abnormal kidney morphology	Ces1d<em1(IMPC)Mbp>/Ces1d<em1(IMPC)Mbp>	C57BL/6NCrl-Ces1d<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262113	F	MP:0011239	abnormal skin coloration	Ces1f<tm1b(KOMP)Wtsi>/Ces1f<tm1b(KOMP)Wtsi>	C57BL/6N-Ces1f<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262113	M	MP:0002590	increased mean corpuscular volume	Ces1f<tm1b(KOMP)Wtsi>/Ces1f<tm1b(KOMP)Wtsi>	C57BL/6N-Ces1f<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262114	F	MP:0001926	female infertility	Cfap206<em1(IMPC)Mbp>/Cfap206<em1(IMPC)Mbp>	C57BL/6NCrl-Cfap206<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262114	M	MP:0001925	male infertility	Cfap206<em1(IMPC)Mbp>/Cfap206<em1(IMPC)Mbp>	C57BL/6NCrl-Cfap206<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262115	M	MP:0001925	male infertility	Cfap44<tm1a(EUCOMM)Wtsi>/Cfap44<tm1a(EUCOMM)Wtsi>	C57BL/6N-Cfap44<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262117	F	MP:0002135	abnormal kidney morphology	Cfb<tm1.1(KOMP)Wtsi>/Cfb<tm1.1(KOMP)Wtsi>	C57BL/6N-Cfb<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262117	M	MP:0000274	enlarged heart	Cfb<tm1.1(KOMP)Wtsi>/Cfb<tm1.1(KOMP)Wtsi>	C57BL/6N-Cfb<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262120	M	MP:0000438	abnormal cranium morphology	Cgrrf1<tm1b(KOMP)Wtsi>/Cgrrf1<tm1b(KOMP)Wtsi>	C57BL/6N-Cgrrf1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262120	M	MP:0010124	decreased bone mineral content	Cgrrf1<tm1b(KOMP)Wtsi>/Cgrrf1<tm1b(KOMP)Wtsi>	C57BL/6N-Cgrrf1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262121	M	MP:0001147	small testis	Ch25h<tm1.1(KOMP)Vlcg>/Ch25h<tm1.1(KOMP)Vlcg>	C57BL/6N-Ch25h<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262121	F	MP:0001126	abnormal ovary morphology	Ch25h<tm1.1(KOMP)Vlcg>/Ch25h<tm1.1(KOMP)Vlcg>	C57BL/6N-Ch25h<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262121	M	MP:0001146	abnormal testis morphology	Ch25h<tm1.1(KOMP)Vlcg>/Ch25h<tm1.1(KOMP)Vlcg>	C57BL/6N-Ch25h<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262122	M	MP:0001147	small testis	Chchd10<em1(IMPC)Mbp>/Chchd10<em1(IMPC)Mbp>	C57BL/6NCrl-Chchd10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262122	F	MP:0001566	increased circulating phosphate level	Chchd10<em1(IMPC)Mbp>/Chchd10<em1(IMPC)Mbp>	C57BL/6NCrl-Chchd10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262122	M	MP:0001146	abnormal testis morphology	Chchd10<em1(IMPC)Mbp>/Chchd10<em1(IMPC)Mbp>	C57BL/6NCrl-Chchd10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262125	F	MP:0000702	enlarged lymph nodes	Chchd7<em3(IMPC)Tcp>/Chchd7<em3(IMPC)Tcp>	C57BL/6NCrl-Chchd7<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262125	M	MP:0001175	abnormal lung morphology	Chchd7<em3(IMPC)Tcp>/Chchd7<em3(IMPC)Tcp>	C57BL/6NCrl-Chchd7<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262126	M	MP:0000198	decreased circulating phosphate level	Chd3<em1(IMPC)J>/Chd3<em1(IMPC)J>	C57BL/6NJ-Chd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262126	F	MP:0001399	hyperactivity	Chd3<em1(IMPC)J>/Chd3<em1(IMPC)J>	C57BL/6NJ-Chd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262127	F	MP:0001926	female infertility	Chdh<tm1b(KOMP)Mbp>/Chdh<tm1b(KOMP)Mbp>	C57BL/6N-Chdh<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6262127	F	MP:0002942	decreased circulating alanine transaminase level	Chdh<tm1b(KOMP)Mbp>/Chdh<tm1b(KOMP)Mbp>	C57BL/6N-Chdh<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6262127	M	MP:0001925	male infertility	Chdh<tm1b(KOMP)Mbp>/Chdh<tm1b(KOMP)Mbp>	C57BL/6N-Chdh<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6262132	F	MP:0002764	short tibia	Chpf<tm1b(EUCOMM)Hmgu>/Chpf<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chpf<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262132	M	MP:0000559	abnormal femur morphology	Chpf<tm1b(EUCOMM)Hmgu>/Chpf<tm1b(EUCOMM)Hmgu>	C57BL/6N-Chpf<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262134	F	MP:0013279	increased fasting circulating glucose level	Chrdl1<em1(IMPC)H>/Chrdl1<em1(IMPC)H>	C57BL/6NTac-Chrdl1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262134	F	MP:0001399	hyperactivity	Chrdl1<em1(IMPC)H>/Chrdl1<em1(IMPC)H>	C57BL/6NTac-Chrdl1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262134	F	MP:0010392	prolonged QRS complex duration	Chrdl1<em1(IMPC)H>/Chrdl1<em1(IMPC)H>	C57BL/6NTac-Chrdl1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262135	M	MP:0001488	increased startle reflex	Chrm4<tm1b(EUCOMM)Hmgu>/Chrm4<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Chrm4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262136	M	MP:0001417	decreased exploration in new environment	Chst14<em1(IMPC)Tcp>/Chst14<+>	C57BL/6NCrl-Chst14<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262137	F	MP:0011100	preweaning lethality, complete penetrance	Chst14<em1(IMPC)Tcp>/Chst14<em1(IMPC)Tcp>	C57BL/6NCrl-Chst14<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262138	F	MP:0005385	cardiovascular system phenotype	Chst5<tm1b(EUCOMM)Wtsi>/Chst5<+>	C57BL/6N-Chst5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262138	F	MP:0003928	increased heart rate variability	Chst5<tm1b(EUCOMM)Wtsi>/Chst5<+>	C57BL/6N-Chst5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262138	M	MP:0001417	decreased exploration in new environment	Chst5<tm1b(EUCOMM)Wtsi>/Chst5<+>	C57BL/6N-Chst5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262140	M	MP:0002060	abnormal skin morphology	Chsy3<em2(IMPC)Mbp>/Chsy3<em2(IMPC)Mbp>	C57BL/6NCrl-Chsy3<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262140	F	MP:0002135	abnormal kidney morphology	Chsy3<em2(IMPC)Mbp>/Chsy3<em2(IMPC)Mbp>	C57BL/6NCrl-Chsy3<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262140	M	MP:0010053	decreased grip strength	Chsy3<em2(IMPC)Mbp>/Chsy3<em2(IMPC)Mbp>	C57BL/6NCrl-Chsy3<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262140	F	MP:0003068	enlarged kidney	Chsy3<em2(IMPC)Mbp>/Chsy3<em2(IMPC)Mbp>	C57BL/6NCrl-Chsy3<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262140	M	MP:0001925	male infertility	Chsy3<em2(IMPC)Mbp>/Chsy3<em2(IMPC)Mbp>	C57BL/6NCrl-Chsy3<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262140	M	MP:0003960	increased lean body mass	Chsy3<em2(IMPC)Mbp>/Chsy3<em2(IMPC)Mbp>	C57BL/6NCrl-Chsy3<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262140	M	MP:0010025	decreased total body fat amount	Chsy3<em2(IMPC)Mbp>/Chsy3<em2(IMPC)Mbp>	C57BL/6NCrl-Chsy3<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262140	F	MP:0001926	female infertility	Chsy3<em2(IMPC)Mbp>/Chsy3<em2(IMPC)Mbp>	C57BL/6NCrl-Chsy3<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262140	M	MP:0002092	abnormal eye morphology	Chsy3<em2(IMPC)Mbp>/Chsy3<em2(IMPC)Mbp>	C57BL/6NCrl-Chsy3<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262140	M	MP:0001200	thick skin	Chsy3<em2(IMPC)Mbp>/Chsy3<em2(IMPC)Mbp>	C57BL/6NCrl-Chsy3<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262141	F	MP:0001392	abnormal locomotor behavior	Cib1<tm1b(EUCOMM)Hmgu>/Cib1<+>	C57BL/6N-Cib1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262142	M	MP:0001925	male infertility	Cib1<tm1b(EUCOMM)Hmgu>/Cib1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cib1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262142	F	MP:0005012	decreased eosinophil cell number	Cib1<tm1b(EUCOMM)Hmgu>/Cib1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cib1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262142	F	MP:0010052	increased grip strength	Cib1<tm1b(EUCOMM)Hmgu>/Cib1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cib1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262142	M	MP:0002608	increased hematocrit	Cib1<tm1b(EUCOMM)Hmgu>/Cib1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cib1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262142	F	MP:0000222	decreased neutrophil cell number	Cib1<tm1b(EUCOMM)Hmgu>/Cib1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cib1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262143	M	MP:0008806	increased circulating amylase level	Cib3<em1(IMPC)H>/Cib3<em1(IMPC)H>	C57BL/6N-Cib3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262143	F	MP:0002102	abnormal ear morphology	Cib3<em1(IMPC)H>/Cib3<em1(IMPC)H>	C57BL/6N-Cib3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262143	F	MP:0001304	cataract	Cib3<em1(IMPC)H>/Cib3<em1(IMPC)H>	C57BL/6N-Cib3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262143	F	MP:0001417	decreased exploration in new environment	Cib3<em1(IMPC)H>/Cib3<em1(IMPC)H>	C57BL/6N-Cib3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262146	F	MP:0003731	abnormal retina outer nuclear layer morphology	Ckap5<tm2b(EUCOMM)Hmgu>/Ckap5<+>	C57BL/6N-Ckap5<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262146	F	MP:0005534	decreased body temperature	Ckap5<tm2b(EUCOMM)Hmgu>/Ckap5<+>	C57BL/6N-Ckap5<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262148	F	MP:0010123	increased bone mineral content	Ckb<tm1.1(KOMP)Wtsi>/Ckb<tm1.1(KOMP)Wtsi>	C57BL/6N-Ckb<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262148	F	MP:0002098	abnormal vibrissa morphology	Ckb<tm1.1(KOMP)Wtsi>/Ckb<tm1.1(KOMP)Wtsi>	C57BL/6N-Ckb<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262148	F	MP:0010067	increased red blood cell distribution width	Ckb<tm1.1(KOMP)Wtsi>/Ckb<tm1.1(KOMP)Wtsi>	C57BL/6N-Ckb<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262148	M	MP:0002175	decreased brain weight	Ckb<tm1.1(KOMP)Wtsi>/Ckb<tm1.1(KOMP)Wtsi>	C57BL/6N-Ckb<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262148	F	MP:0009142	decreased prepulse inhibition	Ckb<tm1.1(KOMP)Wtsi>/Ckb<tm1.1(KOMP)Wtsi>	C57BL/6N-Ckb<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262148	F	MP:0002590	increased mean corpuscular volume	Ckb<tm1.1(KOMP)Wtsi>/Ckb<tm1.1(KOMP)Wtsi>	C57BL/6N-Ckb<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262149	F	MP:0011100	preweaning lethality, complete penetrance	Clasp1<em1(IMPC)Mbp>/Clasp1<em1(IMPC)Mbp>	C57BL/6NCrl-Clasp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262150	F	MP:0001102	small superior vagus ganglion	Clca1<em2(IMPC)Mbp>/Clca1<em2(IMPC)Mbp>	C57BL/6N-Clca1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262150	F	MP:0009709	hydrometra	Clca1<em2(IMPC)Mbp>/Clca1<em2(IMPC)Mbp>	C57BL/6N-Clca1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262150	F	MP:0002098	abnormal vibrissa morphology	Clca1<em2(IMPC)Mbp>/Clca1<em2(IMPC)Mbp>	C57BL/6N-Clca1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	F	MP:0000470	abnormal stomach morphology	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	M	MP:0001147	small testis	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	F	MP:0002606	increased basophil cell number	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	F	MP:0002968	increased circulating alkaline phosphatase level	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	F	MP:0001126	abnormal ovary morphology	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	M	MP:0003068	enlarged kidney	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	F	MP:0010393	shortened QRS complex duration	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	M	MP:0005016	decreased lymphocyte cell number	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	F	MP:0001944	abnormal pancreas morphology	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	F	MP:0005278	abnormal cholesterol homeostasis	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	M	MP:0000599	enlarged liver	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	F	MP:0002989	small kidney	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	M	MP:0010067	increased red blood cell distribution width	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	F	MP:0000277	abnormal heart shape	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262153	F	MP:0005178	increased circulating cholesterol level	Clcnkb<em1(IMPC)Mbp>/Clcnkb<em1(IMPC)Mbp>	C57BL/6NCrl-Clcnkb<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6262154	M	MP:0001289	persistence of hyaloid vascular system	Cldn13<em1(IMPC)J>/Cldn13<em1(IMPC)J>	C57BL/6NJ-Cldn13<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262154	F	MP:0010053	decreased grip strength	Cldn13<em1(IMPC)J>/Cldn13<em1(IMPC)J>	C57BL/6NJ-Cldn13<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262154	M	MP:0002941	increased circulating alanine transaminase level	Cldn13<em1(IMPC)J>/Cldn13<em1(IMPC)J>	C57BL/6NJ-Cldn13<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262154	M	MP:0002075	abnormal coat/hair pigmentation	Cldn13<em1(IMPC)J>/Cldn13<em1(IMPC)J>	C57BL/6NJ-Cldn13<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262155	F	MP:0010067	increased red blood cell distribution width	Cldn18<tm1.1(KOMP)Vlcg>/Cldn18<tm1.1(KOMP)Vlcg>	C57BL/6N-Cldn18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262155	F	MP:0001120	abnormal uterus morphology	Cldn18<tm1.1(KOMP)Vlcg>/Cldn18<tm1.1(KOMP)Vlcg>	C57BL/6N-Cldn18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262155	M	MP:0005630	increased lung weight	Cldn18<tm1.1(KOMP)Vlcg>/Cldn18<tm1.1(KOMP)Vlcg>	C57BL/6N-Cldn18<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262156	F	MP:0010053	decreased grip strength	Clec3b<tm1b(KOMP)Wtsi>/Clec3b<tm1b(KOMP)Wtsi>	B6N(Cg)-Clec3b<tm1b(KOMP)Wtsi>/3J	N	MGI:5576271
MGI:6262158	F	MP:0001120	abnormal uterus morphology	Clec4a4<tm1(KOMP)Vlcg>/Clec4a4<tm1(KOMP)Vlcg>	C57BL/6N-Clec4a4<tm1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262158	F	MP:0009709	hydrometra	Clec4a4<tm1(KOMP)Vlcg>/Clec4a4<tm1(KOMP)Vlcg>	C57BL/6N-Clec4a4<tm1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262159	F	MP:0001102	small superior vagus ganglion	Clps<tm1b(EUCOMM)Wtsi>/Clps<+>	C57BL/6N-Clps<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262159	M	MP:0000274	enlarged heart	Clps<tm1b(EUCOMM)Wtsi>/Clps<+>	C57BL/6N-Clps<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262159	F	MP:0009709	hydrometra	Clps<tm1b(EUCOMM)Wtsi>/Clps<+>	C57BL/6N-Clps<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262159	M	MP:0000266	abnormal heart morphology	Clps<tm1b(EUCOMM)Wtsi>/Clps<+>	C57BL/6N-Clps<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262161	F	MP:0010124	decreased bone mineral content	Clptm1l<em1(IMPC)J>/Clptm1l<em1(IMPC)J>	C57BL/6NJ-Clptm1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262161	F	MP:0001417	decreased exploration in new environment	Clptm1l<em1(IMPC)J>/Clptm1l<em1(IMPC)J>	C57BL/6NJ-Clptm1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262161	F	MP:0001402	decreased locomotor activity	Clptm1l<em1(IMPC)J>/Clptm1l<em1(IMPC)J>	C57BL/6NJ-Clptm1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262161	F	MP:0001304	cataract	Clptm1l<em1(IMPC)J>/Clptm1l<em1(IMPC)J>	C57BL/6NJ-Clptm1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262161	M	MP:0002574	increased vertical activity	Clptm1l<em1(IMPC)J>/Clptm1l<em1(IMPC)J>	C57BL/6NJ-Clptm1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262161	M	MP:0009141	increased prepulse inhibition	Clptm1l<em1(IMPC)J>/Clptm1l<em1(IMPC)J>	C57BL/6NJ-Clptm1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262163	F	MP:0002574	increased vertical activity	Clstn2<em1(IMPC)J>/Clstn2<em1(IMPC)J>	C57BL/6NJ-Clstn2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262166	F	MP:0010097	abnormal retina blood vessel morphology	Cmpk1<tm1b(EUCOMM)Wtsi>/Cmpk1<+>	C57BL/6N-Cmpk1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262166	M	MP:0008528	polycystic kidney	Cmpk1<tm1b(EUCOMM)Wtsi>/Cmpk1<+>	C57BL/6N-Cmpk1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262166	F	MP:0008810	increased circulating iron level	Cmpk1<tm1b(EUCOMM)Wtsi>/Cmpk1<+>	C57BL/6N-Cmpk1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262168	M	MP:0001700	abnormal embryo turning	Cmtr2<tm1.1(KOMP)Vlcg>/Cmtr2<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cmtr2<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:6262169	M	MP:0000598	abnormal liver morphology	Cndp2<em1(IMPC)Mbp>/Cndp2<em1(IMPC)Mbp>	C57BL/6NCrl-Cndp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262169	M	MP:0002997	enlarged seminal vesicle	Cndp2<em1(IMPC)Mbp>/Cndp2<em1(IMPC)Mbp>	C57BL/6NCrl-Cndp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262169	M	MP:0002339	abnormal lymph node morphology	Cndp2<em1(IMPC)Mbp>/Cndp2<em1(IMPC)Mbp>	C57BL/6NCrl-Cndp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262169	M	MP:0000274	enlarged heart	Cndp2<em1(IMPC)Mbp>/Cndp2<em1(IMPC)Mbp>	C57BL/6NCrl-Cndp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262169	M	MP:0000702	enlarged lymph nodes	Cndp2<em1(IMPC)Mbp>/Cndp2<em1(IMPC)Mbp>	C57BL/6NCrl-Cndp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262169	M	MP:0000266	abnormal heart morphology	Cndp2<em1(IMPC)Mbp>/Cndp2<em1(IMPC)Mbp>	C57BL/6NCrl-Cndp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262169	F	MP:0001293	anophthalmia	Cndp2<em1(IMPC)Mbp>/Cndp2<em1(IMPC)Mbp>	C57BL/6NCrl-Cndp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262169	F	MP:0001944	abnormal pancreas morphology	Cndp2<em1(IMPC)Mbp>/Cndp2<em1(IMPC)Mbp>	C57BL/6NCrl-Cndp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262169	M	MP:0002060	abnormal skin morphology	Cndp2<em1(IMPC)Mbp>/Cndp2<em1(IMPC)Mbp>	C57BL/6NCrl-Cndp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262169	F	MP:0002092	abnormal eye morphology	Cndp2<em1(IMPC)Mbp>/Cndp2<em1(IMPC)Mbp>	C57BL/6NCrl-Cndp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262169	M	MP:0001146	abnormal testis morphology	Cndp2<em1(IMPC)Mbp>/Cndp2<em1(IMPC)Mbp>	C57BL/6NCrl-Cndp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262170	F	MP:0000691	enlarged spleen	Cnga3<tm1.1(KOMP)Vlcg>/Cnga3<+>	C57BL/6N-Cnga3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262170	F	MP:0004906	enlarged uterus	Cnga3<tm1.1(KOMP)Vlcg>/Cnga3<+>	C57BL/6N-Cnga3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262171	F	MP:0002941	increased circulating alanine transaminase level	Cnga3<tm1.1(KOMP)Vlcg>/Cnga3<tm1.1(KOMP)Vlcg>	C57BL/6N-Cnga3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262171	M	MP:0011110	preweaning lethality, incomplete penetrance	Cnga3<tm1.1(KOMP)Vlcg>/Cnga3<tm1.1(KOMP)Vlcg>	C57BL/6N-Cnga3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262171	F	MP:0001258	decreased body length	Cnga3<tm1.1(KOMP)Vlcg>/Cnga3<tm1.1(KOMP)Vlcg>	C57BL/6N-Cnga3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262171	F	MP:0002135	abnormal kidney morphology	Cnga3<tm1.1(KOMP)Vlcg>/Cnga3<tm1.1(KOMP)Vlcg>	C57BL/6N-Cnga3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262172	F	MP:0003795	abnormal bone structure	Cnih2<tm1b(KOMP)Wtsi>/Cnih2<tm1b(KOMP)Wtsi>	B6N(Cg)-Cnih2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262172	F	MP:0002574	increased vertical activity	Cnih2<tm1b(KOMP)Wtsi>/Cnih2<tm1b(KOMP)Wtsi>	B6N(Cg)-Cnih2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262174	M	MP:0005293	impaired glucose tolerance	Cnksr2<em1(IMPC)J>/Y	C57BL/6NJ-Cnksr2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262175	F	MP:0000274	enlarged heart	Cnnm2<tm1.1(KOMP)Vlcg>/Cnnm2<+>	C57BL/6N-Cnnm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262175	F	MP:0000062	increased bone mineral density	Cnnm2<tm1.1(KOMP)Vlcg>/Cnnm2<+>	C57BL/6N-Cnnm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262175	F	MP:0000266	abnormal heart morphology	Cnnm2<tm1.1(KOMP)Vlcg>/Cnnm2<+>	C57BL/6N-Cnnm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262175	F	MP:0001399	hyperactivity	Cnnm2<tm1.1(KOMP)Vlcg>/Cnnm2<+>	C57BL/6N-Cnnm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262176	M	MP:0003984	embryonic growth retardation	Cnot10<em1(IMPC)J>/Cnot10<em1(IMPC)J>	C57BL/6NJ-Cnot10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262177	F	MP:0000218	increased leukocyte cell number	Cnppd1<tm1.1(KOMP)Vlcg>/Cnppd1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cnppd1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262177	F	MP:0005562	decreased mean corpuscular hemoglobin	Cnppd1<tm1.1(KOMP)Vlcg>/Cnppd1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cnppd1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262178	M	MP:0001146	abnormal testis morphology	Cntd1<em1(IMPC)Mbp>/Cntd1<em1(IMPC)Mbp>	C57BL/6NCrl-Cntd1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262178	F	MP:0001926	female infertility	Cntd1<em1(IMPC)Mbp>/Cntd1<em1(IMPC)Mbp>	C57BL/6NCrl-Cntd1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262178	M	MP:0001147	small testis	Cntd1<em1(IMPC)Mbp>/Cntd1<em1(IMPC)Mbp>	C57BL/6NCrl-Cntd1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262178	M	MP:0001925	male infertility	Cntd1<em1(IMPC)Mbp>/Cntd1<em1(IMPC)Mbp>	C57BL/6NCrl-Cntd1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262182	F	MP:0000208	decreased hematocrit	Cntnap5a<em1(IMPC)J>/Cntnap5a<em1(IMPC)J>	C57BL/6NJ-Cntnap5a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262182	M	MP:0010024	increased total body fat amount	Cntnap5a<em1(IMPC)J>/Cntnap5a<em1(IMPC)J>	C57BL/6NJ-Cntnap5a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262182	M	MP:0003961	decreased lean body mass	Cntnap5a<em1(IMPC)J>/Cntnap5a<em1(IMPC)J>	C57BL/6NJ-Cntnap5a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262182	M	MP:0009142	decreased prepulse inhibition	Cntnap5a<em1(IMPC)J>/Cntnap5a<em1(IMPC)J>	C57BL/6NJ-Cntnap5a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262185	F	MP:0002591	decreased mean corpuscular volume	Col11a2<tm1b(KOMP)Wtsi>/Col11a2<+>	C57BL/6N-Col11a2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262185	F	MP:0003393	decreased cardiac output	Col11a2<tm1b(KOMP)Wtsi>/Col11a2<+>	C57BL/6N-Col11a2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262185	M	MP:0005344	increased circulating bilirubin level	Col11a2<tm1b(KOMP)Wtsi>/Col11a2<+>	C57BL/6N-Col11a2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262185	F	MP:0011896	increased circulating unsaturated transferrin level	Col11a2<tm1b(KOMP)Wtsi>/Col11a2<+>	C57BL/6N-Col11a2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262185	M	MP:0003960	increased lean body mass	Col11a2<tm1b(KOMP)Wtsi>/Col11a2<+>	C57BL/6N-Col11a2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262185	M	MP:0001488	increased startle reflex	Col11a2<tm1b(KOMP)Wtsi>/Col11a2<+>	C57BL/6N-Col11a2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262185	M	MP:0002644	decreased circulating triglyceride level	Col11a2<tm1b(KOMP)Wtsi>/Col11a2<+>	C57BL/6N-Col11a2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262186	M	MP:0010053	decreased grip strength	Col16a1<em1(IMPC)J>/Col16a1<em1(IMPC)J>	C57BL/6NJ-Col16a1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262186	M	MP:0001304	cataract	Col16a1<em1(IMPC)J>/Col16a1<em1(IMPC)J>	C57BL/6NJ-Col16a1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262187	M	MP:0010067	increased red blood cell distribution width	Col26a1<em3(IMPC)Tcp>/Col26a1<em3(IMPC)Tcp>	C57BL/6NCrl-Col26a1<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262187	M	MP:0020421	increased freezing behavior	Col26a1<em3(IMPC)Tcp>/Col26a1<em3(IMPC)Tcp>	C57BL/6NCrl-Col26a1<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262187	M	MP:0000702	enlarged lymph nodes	Col26a1<em3(IMPC)Tcp>/Col26a1<em3(IMPC)Tcp>	C57BL/6NCrl-Col26a1<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262189	M	MP:0002764	short tibia	Colec10<em2(IMPC)Tcp>/Colec10<em2(IMPC)Tcp>	C57BL/6NCrl-Colec10<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262189	F	MP:0001552	increased circulating triglyceride level	Colec10<em2(IMPC)Tcp>/Colec10<em2(IMPC)Tcp>	C57BL/6NCrl-Colec10<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262189	M	MP:0005270	abnormal zygomatic bone morphology	Colec10<em2(IMPC)Tcp>/Colec10<em2(IMPC)Tcp>	C57BL/6NCrl-Colec10<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262189	M	MP:0000137	abnormal vertebrae morphology	Colec10<em2(IMPC)Tcp>/Colec10<em2(IMPC)Tcp>	C57BL/6NCrl-Colec10<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262189	M	MP:0001566	increased circulating phosphate level	Colec10<em2(IMPC)Tcp>/Colec10<em2(IMPC)Tcp>	C57BL/6NCrl-Colec10<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262189	F	MP:0001120	abnormal uterus morphology	Colec10<em2(IMPC)Tcp>/Colec10<em2(IMPC)Tcp>	C57BL/6NCrl-Colec10<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262189	M	MP:0001417	decreased exploration in new environment	Colec10<em2(IMPC)Tcp>/Colec10<em2(IMPC)Tcp>	C57BL/6NCrl-Colec10<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262189	M	MP:0001258	decreased body length	Colec10<em2(IMPC)Tcp>/Colec10<em2(IMPC)Tcp>	C57BL/6NCrl-Colec10<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262190	F	MP:0009709	hydrometra	Cops7a<tm1b(KOMP)Mbp>/Cops7a<tm1b(KOMP)Mbp>	C57BL/6N-Cops7a<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262190	F	MP:0004924	abnormal behavior	Cops7a<tm1b(KOMP)Mbp>/Cops7a<tm1b(KOMP)Mbp>	C57BL/6N-Cops7a<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262190	F	MP:0020870	decreased thigmotaxis	Cops7a<tm1b(KOMP)Mbp>/Cops7a<tm1b(KOMP)Mbp>	C57BL/6N-Cops7a<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262190	M	MP:0000538	abnormal urinary bladder morphology	Cops7a<tm1b(KOMP)Mbp>/Cops7a<tm1b(KOMP)Mbp>	C57BL/6N-Cops7a<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262190	M	MP:0005292	improved glucose tolerance	Cops7a<tm1b(KOMP)Mbp>/Cops7a<tm1b(KOMP)Mbp>	C57BL/6N-Cops7a<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262190	F	MP:0001399	hyperactivity	Cops7a<tm1b(KOMP)Mbp>/Cops7a<tm1b(KOMP)Mbp>	C57BL/6N-Cops7a<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262190	M	MP:0001925	male infertility	Cops7a<tm1b(KOMP)Mbp>/Cops7a<tm1b(KOMP)Mbp>	C57BL/6N-Cops7a<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262190	F	MP:0001120	abnormal uterus morphology	Cops7a<tm1b(KOMP)Mbp>/Cops7a<tm1b(KOMP)Mbp>	C57BL/6N-Cops7a<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262191	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Coq8b<tm1b(EUCOMM)Hmgu>/Coq8b<+>	B6N(Cg)-Coq8b<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262191	F	MP:0001402	decreased locomotor activity	Coq8b<tm1b(EUCOMM)Hmgu>/Coq8b<+>	B6N(Cg)-Coq8b<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262191	M	MP:0005293	impaired glucose tolerance	Coq8b<tm1b(EUCOMM)Hmgu>/Coq8b<+>	B6N(Cg)-Coq8b<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262191	M	MP:0013278	decreased fasting circulating glucose level	Coq8b<tm1b(EUCOMM)Hmgu>/Coq8b<+>	B6N(Cg)-Coq8b<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262193	F	MP:0001175	abnormal lung morphology	Cox20<em1(IMPC)Tcp>/Cox20<+>	C57BL/6NCrl-Cox20<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262193	M	MP:0001488	increased startle reflex	Cox20<em1(IMPC)Tcp>/Cox20<+>	C57BL/6NCrl-Cox20<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262193	F	MP:0000470	abnormal stomach morphology	Cox20<em1(IMPC)Tcp>/Cox20<+>	C57BL/6NCrl-Cox20<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262193	F	MP:0002989	small kidney	Cox20<em1(IMPC)Tcp>/Cox20<+>	C57BL/6NCrl-Cox20<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262195	F	MP:0002060	abnormal skin morphology	Cox6b1<em1(IMPC)Tcp>/Cox6b1<+>	C57BL/6NCrl-Cox6b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262195	F	MP:0004952	increased spleen weight	Cox6b1<em1(IMPC)Tcp>/Cox6b1<+>	C57BL/6NCrl-Cox6b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262195	F	MP:0005313	absent adrenal gland	Cox6b1<em1(IMPC)Tcp>/Cox6b1<+>	C57BL/6NCrl-Cox6b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262195	F	MP:0004122	abnormal sinus arrhythmia	Cox6b1<em1(IMPC)Tcp>/Cox6b1<+>	C57BL/6NCrl-Cox6b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262196	F	MP:0001297	microphthalmia	Cox6b1<em1(IMPC)Tcp>/Cox6b1<em1(IMPC)Tcp>	C57BL/6NCrl-Cox6b1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262197	M	MP:0000195	decreased circulating calcium level	Cpeb4<tm1b(EUCOMM)Wtsi>/Cpeb4<+>	C57BL/6N-Cpeb4<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262197	M	MP:0002059	abnormal seminal vesicle morphology	Cpeb4<tm1b(EUCOMM)Wtsi>/Cpeb4<+>	C57BL/6N-Cpeb4<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262200	M	MP:0002060	abnormal skin morphology	Cpne7<em1(IMPC)Mbp>/Cpne7<em1(IMPC)Mbp>	C57BL/6NCrl-Cpne7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262200	F	MP:0010123	increased bone mineral content	Cpne7<em1(IMPC)Mbp>/Cpne7<em1(IMPC)Mbp>	C57BL/6NCrl-Cpne7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262200	F	MP:0003795	abnormal bone structure	Cpne7<em1(IMPC)Mbp>/Cpne7<em1(IMPC)Mbp>	C57BL/6NCrl-Cpne7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262200	F	MP:0000494	abnormal cecum morphology	Cpne7<em1(IMPC)Mbp>/Cpne7<em1(IMPC)Mbp>	C57BL/6NCrl-Cpne7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262201	M	MP:0005013	increased lymphocyte cell number	Cps1<em1(IMPC)H>/Cps1<+>	C57BL/6NTac-Cps1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262201	M	MP:0000222	decreased neutrophil cell number	Cps1<em1(IMPC)H>/Cps1<+>	C57BL/6NTac-Cps1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262201	F	MP:0005628	decreased circulating potassium level	Cps1<em1(IMPC)H>/Cps1<+>	C57BL/6NTac-Cps1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262201	M	MP:0005505	thrombocytosis	Cps1<em1(IMPC)H>/Cps1<+>	C57BL/6NTac-Cps1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262201	F	MP:0010052	increased grip strength	Cps1<em1(IMPC)H>/Cps1<+>	C57BL/6NTac-Cps1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262203	M	MP:0002060	abnormal skin morphology	Cpvl<em1(IMPC)Tcp>/Cpvl<em1(IMPC)Tcp>	C57BL/6NCrl-Cpvl<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262203	M	MP:0000702	enlarged lymph nodes	Cpvl<em1(IMPC)Tcp>/Cpvl<em1(IMPC)Tcp>	C57BL/6NCrl-Cpvl<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262203	M	MP:0001200	thick skin	Cpvl<em1(IMPC)Tcp>/Cpvl<em1(IMPC)Tcp>	C57BL/6NCrl-Cpvl<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262203	M	MP:0002833	increased heart weight	Cpvl<em1(IMPC)Tcp>/Cpvl<em1(IMPC)Tcp>	C57BL/6NCrl-Cpvl<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262204	F	MP:0001126	abnormal ovary morphology	Crabp1<tm1b(EUCOMM)Wtsi>/Crabp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Crabp1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262204	F	MP:0004832	enlarged ovary	Crabp1<tm1b(EUCOMM)Wtsi>/Crabp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Crabp1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262204	M	MP:0001289	persistence of hyaloid vascular system	Crabp1<tm1b(EUCOMM)Wtsi>/Crabp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Crabp1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262204	F	MP:0000220	increased monocyte cell number	Crabp1<tm1b(EUCOMM)Wtsi>/Crabp1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Crabp1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262206	F	MP:0001258	decreased body length	Creb3<tm1.1(KOMP)Vlcg>/Creb3<+>	C57BL/6N-Creb3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262206	M	MP:0002175	decreased brain weight	Creb3<tm1.1(KOMP)Vlcg>/Creb3<+>	C57BL/6N-Creb3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262206	M	MP:0002631	abnormal epididymis morphology	Creb3<tm1.1(KOMP)Vlcg>/Creb3<+>	C57BL/6N-Creb3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262206	M	MP:0004931	enlarged epididymis	Creb3<tm1.1(KOMP)Vlcg>/Creb3<+>	C57BL/6N-Creb3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262206	F	MP:0001399	hyperactivity	Creb3<tm1.1(KOMP)Vlcg>/Creb3<+>	C57BL/6N-Creb3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262209	F	MP:0001512	trunk curl	Crim1<em1(IMPC)Wtsi>/Crim1<+>	C57BL/6N-Crim1<em1(IMPC)Wtsi>/WtsiOrl	N	MGI:5576271
MGI:6262211	M	MP:0010067	increased red blood cell distribution width	Crlf3<em1(IMPC)Wtsi>/Crlf3<em1(IMPC)Wtsi>	C57BL/6N-Crlf3<em1(IMPC)Wtsi>/WtsiH	N	MGI:5576271
MGI:6262213	M	MP:0000274	enlarged heart	Crygc<tm1.1(KOMP)Vlcg>/Crygc<tm1.1(KOMP)Vlcg>	C57BL/6N-Crygc<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262213	F	MP:0011110	preweaning lethality, incomplete penetrance	Crygc<tm1.1(KOMP)Vlcg>/Crygc<tm1.1(KOMP)Vlcg>	C57BL/6N-Crygc<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262213	M	MP:0001944	abnormal pancreas morphology	Crygc<tm1.1(KOMP)Vlcg>/Crygc<tm1.1(KOMP)Vlcg>	C57BL/6N-Crygc<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262215	M	MP:0005553	increased circulating creatinine level	Csmd1<em1(IMPC)Wtsi>/Csmd1<em1(IMPC)Wtsi>	C57BL/6N-Csmd1<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262215	M	MP:0010099	abnormal thoracic cage shape	Csmd1<em1(IMPC)Wtsi>/Csmd1<em1(IMPC)Wtsi>	C57BL/6N-Csmd1<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262216	M	MP:0002339	abnormal lymph node morphology	Csmd3<em1(IMPC)Mbp>/Csmd3<em1(IMPC)Mbp>	C57BL/6NCrl-Csmd3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262216	F	MP:0010025	decreased total body fat amount	Csmd3<em1(IMPC)Mbp>/Csmd3<em1(IMPC)Mbp>	C57BL/6NCrl-Csmd3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262216	M	MP:0010052	increased grip strength	Csmd3<em1(IMPC)Mbp>/Csmd3<em1(IMPC)Mbp>	C57BL/6NCrl-Csmd3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262216	M	MP:0000689	abnormal spleen morphology	Csmd3<em1(IMPC)Mbp>/Csmd3<em1(IMPC)Mbp>	C57BL/6NCrl-Csmd3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262216	M	MP:0000367	abnormal coat/ hair morphology	Csmd3<em1(IMPC)Mbp>/Csmd3<em1(IMPC)Mbp>	C57BL/6NCrl-Csmd3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262216	M	MP:0000702	enlarged lymph nodes	Csmd3<em1(IMPC)Mbp>/Csmd3<em1(IMPC)Mbp>	C57BL/6NCrl-Csmd3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262216	F	MP:0010053	decreased grip strength	Csmd3<em1(IMPC)Mbp>/Csmd3<em1(IMPC)Mbp>	C57BL/6NCrl-Csmd3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262216	M	MP:0006203	eye hemorrhage	Csmd3<em1(IMPC)Mbp>/Csmd3<em1(IMPC)Mbp>	C57BL/6NCrl-Csmd3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262216	M	MP:0005344	increased circulating bilirubin level	Csmd3<em1(IMPC)Mbp>/Csmd3<em1(IMPC)Mbp>	C57BL/6NCrl-Csmd3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262216	M	MP:0000186	decreased circulating HDL cholesterol level	Csmd3<em1(IMPC)Mbp>/Csmd3<em1(IMPC)Mbp>	C57BL/6NCrl-Csmd3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262216	F	MP:0003960	increased lean body mass	Csmd3<em1(IMPC)Mbp>/Csmd3<em1(IMPC)Mbp>	C57BL/6NCrl-Csmd3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262217	F	MP:0005343	increased circulating aspartate transaminase level	Csnk1g2<tm1b(EUCOMM)Wtsi>/Csnk1g2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Csnk1g2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262217	M	MP:0003928	increased heart rate variability	Csnk1g2<tm1b(EUCOMM)Wtsi>/Csnk1g2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Csnk1g2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262217	F	MP:0002792	abnormal retina vasculature morphology	Csnk1g2<tm1b(EUCOMM)Wtsi>/Csnk1g2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Csnk1g2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262217	F	MP:0010097	abnormal retina blood vessel morphology	Csnk1g2<tm1b(EUCOMM)Wtsi>/Csnk1g2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Csnk1g2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262217	M	MP:0001325	abnormal retina morphology	Csnk1g2<tm1b(EUCOMM)Wtsi>/Csnk1g2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Csnk1g2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262217	F	MP:0005627	increased circulating potassium level	Csnk1g2<tm1b(EUCOMM)Wtsi>/Csnk1g2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Csnk1g2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262217	M	MP:0005559	increased circulating glucose level	Csnk1g2<tm1b(EUCOMM)Wtsi>/Csnk1g2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Csnk1g2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262218	M	MP:0001399	hyperactivity	Cstb<tm1b(EUCOMM)Wtsi>/Cstb<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cstb<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262218	M	MP:0001258	decreased body length	Cstb<tm1b(EUCOMM)Wtsi>/Cstb<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cstb<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262218	F	MP:0011960	abnormal eye anterior chamber depth	Cstb<tm1b(EUCOMM)Wtsi>/Cstb<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cstb<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262218	M	MP:0000220	increased monocyte cell number	Cstb<tm1b(EUCOMM)Wtsi>/Cstb<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cstb<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262218	F	MP:0011965	decreased total retina thickness	Cstb<tm1b(EUCOMM)Wtsi>/Cstb<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cstb<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262218	M	MP:0001552	increased circulating triglyceride level	Cstb<tm1b(EUCOMM)Wtsi>/Cstb<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cstb<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262218	M	MP:0002574	increased vertical activity	Cstb<tm1b(EUCOMM)Wtsi>/Cstb<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cstb<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262219	M	MP:0005293	impaired glucose tolerance	Cs<tm1.1(KOMP)Wtsi>/Cs<+>	C57BL/6N-Cs<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262219	M	MP:0010053	decreased grip strength	Cs<tm1.1(KOMP)Wtsi>/Cs<+>	C57BL/6N-Cs<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262219	M	MP:0002110	abnormal digit morphology	Cs<tm1.1(KOMP)Wtsi>/Cs<+>	C57BL/6N-Cs<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262219	F	MP:0009142	decreased prepulse inhibition	Cs<tm1.1(KOMP)Wtsi>/Cs<+>	C57BL/6N-Cs<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262222	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Ctsm<tm1(KOMP)Wtsi>/Ctsm<tm1(KOMP)Wtsi>	C57BL/6N-Ctsm<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262222	F	MP:0013279	increased fasting circulating glucose level	Ctsm<tm1(KOMP)Wtsi>/Ctsm<tm1(KOMP)Wtsi>	C57BL/6N-Ctsm<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262222	M	MP:0000220	increased monocyte cell number	Ctsm<tm1(KOMP)Wtsi>/Ctsm<tm1(KOMP)Wtsi>	C57BL/6N-Ctsm<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262222	M	MP:0001417	decreased exploration in new environment	Ctsm<tm1(KOMP)Wtsi>/Ctsm<tm1(KOMP)Wtsi>	C57BL/6N-Ctsm<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262224	F	MP:0004222	iris synechia	Cubn<tm1b(EUCOMM)Hmgu>/Cubn<+>	C57BL/6N-Cubn<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262224	F	MP:0001307	fused cornea and lens	Cubn<tm1b(EUCOMM)Hmgu>/Cubn<+>	C57BL/6N-Cubn<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262224	F	MP:0001322	abnormal iris morphology	Cubn<tm1b(EUCOMM)Hmgu>/Cubn<+>	C57BL/6N-Cubn<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262226	M	MP:0000691	enlarged spleen	Cul5<tm1.1(KOMP)Vlcg>/Cul5<+>	C57BL/6N-Cul5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262226	M	MP:0000274	enlarged heart	Cul5<tm1.1(KOMP)Vlcg>/Cul5<+>	C57BL/6N-Cul5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262226	M	MP:0004952	increased spleen weight	Cul5<tm1.1(KOMP)Vlcg>/Cul5<+>	C57BL/6N-Cul5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262226	M	MP:0000266	abnormal heart morphology	Cul5<tm1.1(KOMP)Vlcg>/Cul5<+>	C57BL/6N-Cul5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262226	M	MP:0000689	abnormal spleen morphology	Cul5<tm1.1(KOMP)Vlcg>/Cul5<+>	C57BL/6N-Cul5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262227	F	MP:0003717	pallor	Cul5<tm1.1(KOMP)Vlcg>/Cul5<tm1.1(KOMP)Vlcg>	C57BL/6N-Cul5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262227	F	MP:0003984	embryonic growth retardation	Cul5<tm1.1(KOMP)Vlcg>/Cul5<tm1.1(KOMP)Vlcg>	C57BL/6N-Cul5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262227	F	MP:0001697	abnormal embryo size	Cul5<tm1.1(KOMP)Vlcg>/Cul5<tm1.1(KOMP)Vlcg>	C57BL/6N-Cul5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262227	F	MP:0002151	abnormal neural tube morphology	Cul5<tm1.1(KOMP)Vlcg>/Cul5<tm1.1(KOMP)Vlcg>	C57BL/6N-Cul5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262227	F	MP:0000288	abnormal pericardium morphology	Cul5<tm1.1(KOMP)Vlcg>/Cul5<tm1.1(KOMP)Vlcg>	C57BL/6N-Cul5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262228	M	MP:0011625	cystolithiasis	Cwc22<em1(IMPC)Mbp>/Cwc22<+>	C57BL/6NCrl-Cwc22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262228	F	MP:0000689	abnormal spleen morphology	Cwc22<em1(IMPC)Mbp>/Cwc22<+>	C57BL/6NCrl-Cwc22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262228	M	MP:0009552	urinary bladder obstruction	Cwc22<em1(IMPC)Mbp>/Cwc22<+>	C57BL/6NCrl-Cwc22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262228	F	MP:0010123	increased bone mineral content	Cwc22<em1(IMPC)Mbp>/Cwc22<+>	C57BL/6NCrl-Cwc22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262228	F	MP:0005343	increased circulating aspartate transaminase level	Cwc22<em1(IMPC)Mbp>/Cwc22<+>	C57BL/6NCrl-Cwc22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262230	F	MP:0004906	enlarged uterus	Cxcl12<tm1.1(KOMP)Vlcg>/Cxcl12<+>	C57BL/6N-Cxcl12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262230	M	MP:0003179	thrombocytopenia	Cxcl12<tm1.1(KOMP)Vlcg>/Cxcl12<+>	C57BL/6N-Cxcl12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262230	F	MP:0001120	abnormal uterus morphology	Cxcl12<tm1.1(KOMP)Vlcg>/Cxcl12<+>	C57BL/6N-Cxcl12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262230	F	MP:0009709	hydrometra	Cxcl12<tm1.1(KOMP)Vlcg>/Cxcl12<+>	C57BL/6N-Cxcl12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262233	F	MP:0005554	decreased circulating creatinine level	Cxxc4<em1(IMPC)J>/Cxxc4<em1(IMPC)J>	C57BL/6NJ-Cxxc4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262233	F	MP:0010053	decreased grip strength	Cxxc4<em1(IMPC)J>/Cxxc4<em1(IMPC)J>	C57BL/6NJ-Cxxc4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262233	F	MP:0010124	decreased bone mineral content	Cxxc4<em1(IMPC)J>/Cxxc4<em1(IMPC)J>	C57BL/6NJ-Cxxc4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262234	F	MP:0000689	abnormal spleen morphology	Cyb561d2<tm1b(EUCOMM)Wtsi>/Cyb561d2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561d2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262234	F	MP:0011959	abnormal eye posterior chamber depth	Cyb561d2<tm1b(EUCOMM)Wtsi>/Cyb561d2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyb561d2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262236	F	MP:0001304	cataract	Cyb5r3<tm1b(KOMP)Wtsi>/Cyb5r3<+>	C57BL/6N-Cyb5r3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262236	F	MP:0013278	decreased fasting circulating glucose level	Cyb5r3<tm1b(KOMP)Wtsi>/Cyb5r3<+>	C57BL/6N-Cyb5r3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262238	M	MP:0009453	enhanced contextual conditioning behavior	Cyp21a1<em1(IMPC)Tcp>/Cyp21a1<+>	C57BL/6NCrl-Cyp21a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262238	M	MP:0000691	enlarged spleen	Cyp21a1<em1(IMPC)Tcp>/Cyp21a1<+>	C57BL/6NCrl-Cyp21a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262239	F	MP:0011100	preweaning lethality, complete penetrance	Cyp21a1<em1(IMPC)Tcp>/Cyp21a1<em1(IMPC)Tcp>	C57BL/6NCrl-Cyp21a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262239	M	MP:0003717	pallor	Cyp21a1<em1(IMPC)Tcp>/Cyp21a1<em1(IMPC)Tcp>	C57BL/6NCrl-Cyp21a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262240	M	MP:0002060	abnormal skin morphology	Cyp2d22<em1(IMPC)Tcp>/Cyp2d22<em1(IMPC)Tcp>	C57BL/6NCrl-Cyp2d22<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262240	M	MP:0000702	enlarged lymph nodes	Cyp2d22<em1(IMPC)Tcp>/Cyp2d22<em1(IMPC)Tcp>	C57BL/6NCrl-Cyp2d22<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262240	F	MP:0001402	decreased locomotor activity	Cyp2d22<em1(IMPC)Tcp>/Cyp2d22<em1(IMPC)Tcp>	C57BL/6NCrl-Cyp2d22<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262242	F	MP:0013279	increased fasting circulating glucose level	Cyp4f16<tm1b(KOMP)Wtsi>/Cyp4f16<tm1b(KOMP)Wtsi>	C57BL/6N-Cyp4f16<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262242	M	MP:0001513	limb grasping	Cyp4f16<tm1b(KOMP)Wtsi>/Cyp4f16<tm1b(KOMP)Wtsi>	C57BL/6N-Cyp4f16<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262243	F	MP:0001488	increased startle reflex	Cyp7a1<tm1b(EUCOMM)Wtsi>/Cyp7a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp7a1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262243	F	MP:0000218	increased leukocyte cell number	Cyp7a1<tm1b(EUCOMM)Wtsi>/Cyp7a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp7a1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262243	F	MP:0004151	decreased circulating iron level	Cyp7a1<tm1b(EUCOMM)Wtsi>/Cyp7a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp7a1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262243	F	MP:0005344	increased circulating bilirubin level	Cyp7a1<tm1b(EUCOMM)Wtsi>/Cyp7a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp7a1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262243	M	MP:0011896	increased circulating unsaturated transferrin level	Cyp7a1<tm1b(EUCOMM)Wtsi>/Cyp7a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp7a1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262243	F	MP:0005566	decreased blood urea nitrogen level	Cyp7a1<tm1b(EUCOMM)Wtsi>/Cyp7a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp7a1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262243	F	MP:0001289	persistence of hyaloid vascular system	Cyp7a1<tm1b(EUCOMM)Wtsi>/Cyp7a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp7a1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262243	M	MP:0005419	decreased circulating serum albumin level	Cyp7a1<tm1b(EUCOMM)Wtsi>/Cyp7a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cyp7a1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262244	F	MP:0002590	increased mean corpuscular volume	D130043K22Rik<tm1b(KOMP)Wtsi>/D130043K22Rik<tm1b(KOMP)Wtsi>	C57BL/6N-D130043K22Rik<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262245	M	MP:0005293	impaired glucose tolerance	Ilrun<em1(IMPC)Tcp>/Ilrun<em1(IMPC)Tcp>	C57BL/6NCrl-Ilrun<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262245	M	MP:0003961	decreased lean body mass	Ilrun<em1(IMPC)Tcp>/Ilrun<em1(IMPC)Tcp>	C57BL/6NCrl-Ilrun<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262246	F	MP:0005568	increased circulating total protein level	D6Wsu163e<tm1b(EUCOMM)Wtsi>/D6Wsu163e<tm1b(EUCOMM)Wtsi>	C57BL/6N-D6Wsu163e<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262246	M	MP:0001556	increased circulating HDL cholesterol level	D6Wsu163e<tm1b(EUCOMM)Wtsi>/D6Wsu163e<tm1b(EUCOMM)Wtsi>	C57BL/6N-D6Wsu163e<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262246	F	MP:0002965	increased circulating serum albumin level	D6Wsu163e<tm1b(EUCOMM)Wtsi>/D6Wsu163e<tm1b(EUCOMM)Wtsi>	C57BL/6N-D6Wsu163e<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262246	F	MP:0000182	increased circulating LDL cholesterol level	D6Wsu163e<tm1b(EUCOMM)Wtsi>/D6Wsu163e<tm1b(EUCOMM)Wtsi>	C57BL/6N-D6Wsu163e<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262246	M	MP:0000063	decreased bone mineral density	D6Wsu163e<tm1b(EUCOMM)Wtsi>/D6Wsu163e<tm1b(EUCOMM)Wtsi>	C57BL/6N-D6Wsu163e<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262246	M	MP:0011939	increased food intake	D6Wsu163e<tm1b(EUCOMM)Wtsi>/D6Wsu163e<tm1b(EUCOMM)Wtsi>	C57BL/6N-D6Wsu163e<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262247	F	MP:0001926	female infertility	D930020B18Rik<tm1.1(KOMP)Vlcg>/D930020B18Rik<tm1.1(KOMP)Vlcg>	C57BL/6N-D930020B18Rik<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262248	M	MP:0005559	increased circulating glucose level	Dbil5<tm1(KOMP)Wtsi>/Dbil5<tm1(KOMP)Wtsi>	C57BL/6N-Dbil5<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262248	F	MP:0002968	increased circulating alkaline phosphatase level	Dbil5<tm1(KOMP)Wtsi>/Dbil5<tm1(KOMP)Wtsi>	C57BL/6N-Dbil5<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262251	F	MP:0001303	abnormal lens morphology	Dbr1<tm1.1(KOMP)Vlcg>/Dbr1<+>	C57BL/6N-Dbr1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262253	F	MP:0005568	increased circulating total protein level	Dcaf7<tm1b(EUCOMM)Wtsi>/Dcaf7<+>	C57BL/6N-Dcaf7<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6262256	M	MP:0001554	increased circulating free fatty acids level	Dctn4<em1(IMPC)Wtsi>/Dctn4<+>	C57BL/6N-Dctn4<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262260	M	MP:0000186	decreased circulating HDL cholesterol level	Dcun1d3<em1(IMPC)Wtsi>/Dcun1d3<em1(IMPC)Wtsi>	C57BL/6N-Dcun1d3<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262260	M	MP:0005179	decreased circulating cholesterol level	Dcun1d3<em1(IMPC)Wtsi>/Dcun1d3<em1(IMPC)Wtsi>	C57BL/6N-Dcun1d3<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262260	M	MP:0010025	decreased total body fat amount	Dcun1d3<em1(IMPC)Wtsi>/Dcun1d3<em1(IMPC)Wtsi>	C57BL/6N-Dcun1d3<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262260	M	MP:0005560	decreased circulating glucose level	Dcun1d3<em1(IMPC)Wtsi>/Dcun1d3<em1(IMPC)Wtsi>	C57BL/6N-Dcun1d3<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262260	F	MP:0002968	increased circulating alkaline phosphatase level	Dcun1d3<em1(IMPC)Wtsi>/Dcun1d3<em1(IMPC)Wtsi>	C57BL/6N-Dcun1d3<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262260	M	MP:0003960	increased lean body mass	Dcun1d3<em1(IMPC)Wtsi>/Dcun1d3<em1(IMPC)Wtsi>	C57BL/6N-Dcun1d3<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262260	M	MP:0010067	increased red blood cell distribution width	Dcun1d3<em1(IMPC)Wtsi>/Dcun1d3<em1(IMPC)Wtsi>	C57BL/6N-Dcun1d3<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262260	M	MP:0013278	decreased fasting circulating glucose level	Dcun1d3<em1(IMPC)Wtsi>/Dcun1d3<em1(IMPC)Wtsi>	C57BL/6N-Dcun1d3<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262260	M	MP:0005292	improved glucose tolerance	Dcun1d3<em1(IMPC)Wtsi>/Dcun1d3<em1(IMPC)Wtsi>	C57BL/6N-Dcun1d3<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262261	M	MP:0000274	enlarged heart	Dcxr<tm1.1(KOMP)Vlcg>/Dcxr<tm1.1(KOMP)Vlcg>	C57BL/6N-Dcxr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262261	M	MP:0000266	abnormal heart morphology	Dcxr<tm1.1(KOMP)Vlcg>/Dcxr<tm1.1(KOMP)Vlcg>	C57BL/6N-Dcxr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262261	F	MP:0011110	preweaning lethality, incomplete penetrance	Dcxr<tm1.1(KOMP)Vlcg>/Dcxr<tm1.1(KOMP)Vlcg>	C57BL/6N-Dcxr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262262	F	MP:0005343	increased circulating aspartate transaminase level	Ddit3<tm1.1(KOMP)Vlcg>/Ddit3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ddit3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262265	M	MP:0001925	male infertility	Ddx19b<em1(IMPC)Mbp>/Ddx19b<em1(IMPC)Mbp>	C57BL/6N-Ddx19b<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262269	M	MP:0001510	abnormal coat appearance	Ddx39a<tm1b(KOMP)Wtsi>/Ddx39a<+>	C57BL/6N-Ddx39a<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262269	F	MP:0011239	abnormal skin coloration	Ddx39a<tm1b(KOMP)Wtsi>/Ddx39a<+>	C57BL/6N-Ddx39a<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262269	F	MP:0009142	decreased prepulse inhibition	Ddx39a<tm1b(KOMP)Wtsi>/Ddx39a<+>	C57BL/6N-Ddx39a<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262270	M	MP:0001711	abnormal placenta morphology	Ddx39a<tm1b(KOMP)Wtsi>/Ddx39a<tm1b(KOMP)Wtsi>	C57BL/6N-Ddx39a<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262270	F	MP:0004258	abnormal placenta size	Ddx39a<tm1b(KOMP)Wtsi>/Ddx39a<tm1b(KOMP)Wtsi>	C57BL/6N-Ddx39a<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262270	M	MP:0003231	abnormal placenta vasculature	Ddx39a<tm1b(KOMP)Wtsi>/Ddx39a<tm1b(KOMP)Wtsi>	C57BL/6N-Ddx39a<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262270	F	MP:0011100	preweaning lethality, complete penetrance	Ddx39a<tm1b(KOMP)Wtsi>/Ddx39a<tm1b(KOMP)Wtsi>	C57BL/6N-Ddx39a<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262272	M	MP:0001925	male infertility	Defb20<tm1b(EUCOMM)Hmgu>/Defb20<tm1b(EUCOMM)Hmgu>	C57BL/6N-Defb20<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262276	M	MP:0000274	enlarged heart	Dgat2l6<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Dgat2l6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262276	M	MP:0000266	abnormal heart morphology	Dgat2l6<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Dgat2l6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262276	M	MP:0002135	abnormal kidney morphology	Dgat2l6<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Dgat2l6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262277	F	MP:0002941	increased circulating alanine transaminase level	Dgat2l6<tm1b(KOMP)Wtsi>/Dgat2l6<tm1b(KOMP)Wtsi>	C57BL/6N-Dgat2l6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262277	F	MP:0005343	increased circulating aspartate transaminase level	Dgat2l6<tm1b(KOMP)Wtsi>/Dgat2l6<tm1b(KOMP)Wtsi>	C57BL/6N-Dgat2l6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262277	F	MP:0001284	absent vibrissae	Dgat2l6<tm1b(KOMP)Wtsi>/Dgat2l6<tm1b(KOMP)Wtsi>	C57BL/6N-Dgat2l6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262278	M	MP:0005554	decreased circulating creatinine level	Dgke<em1(IMPC)Tcp>/Dgke<em1(IMPC)Tcp>	C57BL/6NCrl-Dgke<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262278	M	MP:0000157	abnormal sternum morphology	Dgke<em1(IMPC)Tcp>/Dgke<em1(IMPC)Tcp>	C57BL/6NCrl-Dgke<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262278	M	MP:0001399	hyperactivity	Dgke<em1(IMPC)Tcp>/Dgke<em1(IMPC)Tcp>	C57BL/6NCrl-Dgke<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262278	M	MP:0001146	abnormal testis morphology	Dgke<em1(IMPC)Tcp>/Dgke<em1(IMPC)Tcp>	C57BL/6NCrl-Dgke<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262279	M	MP:0004924	abnormal behavior	Dgkq<tm1b(KOMP)Wtsi>/Dgkq<tm1b(KOMP)Wtsi>	C57BL/6N-Dgkq<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262279	M	MP:0020870	decreased thigmotaxis	Dgkq<tm1b(KOMP)Wtsi>/Dgkq<tm1b(KOMP)Wtsi>	C57BL/6N-Dgkq<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262281	F	MP:0000745	tremors	Dhdds<tm1b(KOMP)Wtsi>/Dhdds<+>	C57BL/6N-Dhdds<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262282	F	MP:0009142	decreased prepulse inhibition	Dhfr<tm1b(EUCOMM)Wtsi>/Dhfr<+>	C57BL/6N-Dhfr<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262282	F	MP:0005562	decreased mean corpuscular hemoglobin	Dhfr<tm1b(EUCOMM)Wtsi>/Dhfr<+>	C57BL/6N-Dhfr<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262287	F	MP:0010123	increased bone mineral content	Dlg4<tm1e(EUCOMM)Wtsi>/Dlg4<tm1e(EUCOMM)Wtsi>	C57BL/6N-Dlg4<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262287	M	MP:0005633	increased circulating sodium level	Dlg4<tm1e(EUCOMM)Wtsi>/Dlg4<tm1e(EUCOMM)Wtsi>	C57BL/6N-Dlg4<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262287	M	MP:0010053	decreased grip strength	Dlg4<tm1e(EUCOMM)Wtsi>/Dlg4<tm1e(EUCOMM)Wtsi>	C57BL/6N-Dlg4<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262288	F	MP:0005553	increased circulating creatinine level	Dlgap4<tm1b(KOMP)Wtsi>/Dlgap4<+>	C57BL/6N-Dlgap4<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262288	M	MP:0013278	decreased fasting circulating glucose level	Dlgap4<tm1b(KOMP)Wtsi>/Dlgap4<+>	C57BL/6N-Dlgap4<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262288	M	MP:0010025	decreased total body fat amount	Dlgap4<tm1b(KOMP)Wtsi>/Dlgap4<+>	C57BL/6N-Dlgap4<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262288	M	MP:0002875	decreased erythrocyte cell number	Dlgap4<tm1b(KOMP)Wtsi>/Dlgap4<+>	C57BL/6N-Dlgap4<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262288	M	MP:0003960	increased lean body mass	Dlgap4<tm1b(KOMP)Wtsi>/Dlgap4<+>	C57BL/6N-Dlgap4<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262289	M	MP:0010024	increased total body fat amount	Dlk1<em1(IMPC)Wtsi>/Dlk1<em1(IMPC)Wtsi>	C57BL/6N-Dlk1<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262290	F	MP:0003068	enlarged kidney	Dmp1<tm1.1(KOMP)Vlcg>/Dmp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dmp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262290	F	MP:0002135	abnormal kidney morphology	Dmp1<tm1.1(KOMP)Vlcg>/Dmp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dmp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262290	F	MP:0005566	decreased blood urea nitrogen level	Dmp1<tm1.1(KOMP)Vlcg>/Dmp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dmp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262290	F	MP:0003795	abnormal bone structure	Dmp1<tm1.1(KOMP)Vlcg>/Dmp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dmp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262290	M	MP:0003960	increased lean body mass	Dmp1<tm1.1(KOMP)Vlcg>/Dmp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dmp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262291	F	MP:0002073	abnormal hair growth	Dnah17<tm1e(KOMP)Wtsi>/Dnah17<tm1e(KOMP)Wtsi>	C57BL/6N-Dnah17<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262291	M	MP:0001925	male infertility	Dnah17<tm1e(KOMP)Wtsi>/Dnah17<tm1e(KOMP)Wtsi>	C57BL/6N-Dnah17<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262292	M	MP:0001510	abnormal coat appearance	Dnah1<tm1b(EUCOMM)Hmgu>/Dnah1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dnah1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262293	F	MP:0001926	female infertility	Dnaja2<em1(IMPC)Mbp>/Dnaja2<em1(IMPC)Mbp>	C57BL/6N-Dnaja2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262294	F	MP:0002968	increased circulating alkaline phosphatase level	Dnajb11<tm1b(EUCOMM)Wtsi>/Dnajb11<+>	C57BL/6N-Dnajb11<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262294	M	MP:0010574	dilated aorta	Dnajb11<tm1b(EUCOMM)Wtsi>/Dnajb11<+>	C57BL/6N-Dnajb11<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262296	F	MP:0001363	increased anxiety-related response	Dnajb2<em1(IMPC)J>/Dnajb2<em1(IMPC)J>	C57BL/6NJ-Dnajb2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262298	F	MP:0002764	short tibia	Dnajc21<tm1.1(NCOM)Mfgc>/Dnajc21<+>	C57BL/6N-Dnajc21<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:6262298	F	MP:0004122	abnormal sinus arrhythmia	Dnajc21<tm1.1(NCOM)Mfgc>/Dnajc21<+>	C57BL/6N-Dnajc21<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:6262299	M	MP:0000194	increased circulating calcium level	Dnajc30<tm1.1(KOMP)Vlcg>/Dnajc30<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajc30<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262299	F	MP:0005292	improved glucose tolerance	Dnajc30<tm1.1(KOMP)Vlcg>/Dnajc30<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajc30<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262299	M	MP:0005568	increased circulating total protein level	Dnajc30<tm1.1(KOMP)Vlcg>/Dnajc30<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnajc30<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262300	M	MP:0000266	abnormal heart morphology	Dnase1l2<em2(IMPC)Mbp>/Dnase1l2<em2(IMPC)Mbp>	C57BL/6N-Dnase1l2<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262300	F	MP:0009709	hydrometra	Dnase1l2<em2(IMPC)Mbp>/Dnase1l2<em2(IMPC)Mbp>	C57BL/6N-Dnase1l2<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262300	M	MP:0000274	enlarged heart	Dnase1l2<em2(IMPC)Mbp>/Dnase1l2<em2(IMPC)Mbp>	C57BL/6N-Dnase1l2<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262300	F	MP:0001102	small superior vagus ganglion	Dnase1l2<em2(IMPC)Mbp>/Dnase1l2<em2(IMPC)Mbp>	C57BL/6N-Dnase1l2<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262301	F	MP:0009709	hydrometra	Dnase1<tm1.1(KOMP)Vlcg>/Dnase1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnase1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262301	F	MP:0000266	abnormal heart morphology	Dnase1<tm1.1(KOMP)Vlcg>/Dnase1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnase1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262301	M	MP:0000538	abnormal urinary bladder morphology	Dnase1<tm1.1(KOMP)Vlcg>/Dnase1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnase1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262301	F	MP:0000274	enlarged heart	Dnase1<tm1.1(KOMP)Vlcg>/Dnase1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnase1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262301	F	MP:0001120	abnormal uterus morphology	Dnase1<tm1.1(KOMP)Vlcg>/Dnase1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dnase1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262302	M	MP:0005343	increased circulating aspartate transaminase level	Dner<tm3b(EUCOMM)Hmgu>/Dner<tm3b(EUCOMM)Hmgu>	C57BL/6N-Dner<tm3b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262304	F	MP:0009709	hydrometra	Dnm2<tm1.1(KOMP)Vlcg>/Dnm2<+>	C57BL/6N-Dnm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262304	F	MP:0001102	small superior vagus ganglion	Dnm2<tm1.1(KOMP)Vlcg>/Dnm2<+>	C57BL/6N-Dnm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262304	F	MP:0004906	enlarged uterus	Dnm2<tm1.1(KOMP)Vlcg>/Dnm2<+>	C57BL/6N-Dnm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262304	F	MP:0002968	increased circulating alkaline phosphatase level	Dnm2<tm1.1(KOMP)Vlcg>/Dnm2<+>	C57BL/6N-Dnm2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262305	F	MP:0000689	abnormal spleen morphology	Dnmbp<em1(IMPC)Mbp>/Dnmbp<em1(IMPC)Mbp>	C57BL/6N-Dnmbp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262305	F	MP:0000691	enlarged spleen	Dnmbp<em1(IMPC)Mbp>/Dnmbp<em1(IMPC)Mbp>	C57BL/6N-Dnmbp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262305	F	MP:0002188	small heart	Dnmbp<em1(IMPC)Mbp>/Dnmbp<em1(IMPC)Mbp>	C57BL/6N-Dnmbp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262305	F	MP:0002989	small kidney	Dnmbp<em1(IMPC)Mbp>/Dnmbp<em1(IMPC)Mbp>	C57BL/6N-Dnmbp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262305	F	MP:0000598	abnormal liver morphology	Dnmbp<em1(IMPC)Mbp>/Dnmbp<em1(IMPC)Mbp>	C57BL/6N-Dnmbp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262305	M	MP:0003642	absent seminal vesicle	Dnmbp<em1(IMPC)Mbp>/Dnmbp<em1(IMPC)Mbp>	C57BL/6N-Dnmbp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262305	M	MP:0002997	enlarged seminal vesicle	Dnmbp<em1(IMPC)Mbp>/Dnmbp<em1(IMPC)Mbp>	C57BL/6N-Dnmbp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262305	F	MP:0000266	abnormal heart morphology	Dnmbp<em1(IMPC)Mbp>/Dnmbp<em1(IMPC)Mbp>	C57BL/6N-Dnmbp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262305	F	MP:0002135	abnormal kidney morphology	Dnmbp<em1(IMPC)Mbp>/Dnmbp<em1(IMPC)Mbp>	C57BL/6N-Dnmbp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262305	M	MP:0002574	increased vertical activity	Dnmbp<em1(IMPC)Mbp>/Dnmbp<em1(IMPC)Mbp>	C57BL/6N-Dnmbp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262307	M	MP:0001289	persistence of hyaloid vascular system	Dnmt3l<tm1b(EUCOMM)Hmgu>/Dnmt3l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dnmt3l<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262307	M	MP:0001147	small testis	Dnmt3l<tm1b(EUCOMM)Hmgu>/Dnmt3l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dnmt3l<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262307	F	MP:0000062	increased bone mineral density	Dnmt3l<tm1b(EUCOMM)Hmgu>/Dnmt3l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Dnmt3l<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262309	M	MP:0003917	increased kidney weight	Dock11<tm2b(KOMP)Wtsi>/Y	C57BL/6N-Dock11<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262309	M	MP:0002092	abnormal eye morphology	Dock11<tm2b(KOMP)Wtsi>/Y	C57BL/6N-Dock11<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262310	M	MP:0005344	increased circulating bilirubin level	Dock6<em1(IMPC)J>/Dock6<+>	C57BL/6NJ-Dock6<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262310	M	MP:0003131	increased erythrocyte cell number	Dock6<em1(IMPC)J>/Dock6<+>	C57BL/6NJ-Dock6<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262310	M	MP:0005564	increased hemoglobin content	Dock6<em1(IMPC)J>/Dock6<+>	C57BL/6NJ-Dock6<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262312	F	MP:0005561	increased mean corpuscular hemoglobin	Dock9<em1(IMPC)J>/Dock9<em1(IMPC)J>	C57BL/6NJ-Dock9<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262312	M	MP:0003960	increased lean body mass	Dock9<em1(IMPC)J>/Dock9<em1(IMPC)J>	C57BL/6NJ-Dock9<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262312	M	MP:0010025	decreased total body fat amount	Dock9<em1(IMPC)J>/Dock9<em1(IMPC)J>	C57BL/6NJ-Dock9<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262312	M	MP:0005344	increased circulating bilirubin level	Dock9<em1(IMPC)J>/Dock9<em1(IMPC)J>	C57BL/6NJ-Dock9<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262312	M	MP:0010123	increased bone mineral content	Dock9<em1(IMPC)J>/Dock9<em1(IMPC)J>	C57BL/6NJ-Dock9<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262313	F	MP:0010053	decreased grip strength	Dpf1<tm1.1(KOMP)Vlcg>/Dpf1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dpf1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262313	F	MP:0001399	hyperactivity	Dpf1<tm1.1(KOMP)Vlcg>/Dpf1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dpf1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262314	M	MP:0000266	abnormal heart morphology	Dpy19l1<em1(IMPC)Mbp>/Dpy19l1<+>	C57BL/6N-Dpy19l1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262314	M	MP:0000274	enlarged heart	Dpy19l1<em1(IMPC)Mbp>/Dpy19l1<+>	C57BL/6N-Dpy19l1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262315	M	MP:0001925	male infertility	Dpy19l1<em1(IMPC)Mbp>/Dpy19l1<em1(IMPC)Mbp>	C57BL/6N-Dpy19l1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262315	M	MP:0002135	abnormal kidney morphology	Dpy19l1<em1(IMPC)Mbp>/Dpy19l1<em1(IMPC)Mbp>	C57BL/6N-Dpy19l1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262315	M	MP:0001157	small seminal vesicle	Dpy19l1<em1(IMPC)Mbp>/Dpy19l1<em1(IMPC)Mbp>	C57BL/6N-Dpy19l1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262315	F	MP:0001926	female infertility	Dpy19l1<em1(IMPC)Mbp>/Dpy19l1<em1(IMPC)Mbp>	C57BL/6N-Dpy19l1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262315	M	MP:0002059	abnormal seminal vesicle morphology	Dpy19l1<em1(IMPC)Mbp>/Dpy19l1<em1(IMPC)Mbp>	C57BL/6N-Dpy19l1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262315	M	MP:0002989	small kidney	Dpy19l1<em1(IMPC)Mbp>/Dpy19l1<em1(IMPC)Mbp>	C57BL/6N-Dpy19l1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262316	M	MP:0001175	abnormal lung morphology	Dram1<tm1.1(KOMP)Vlcg>/Dram1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dram1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262316	F	MP:0010052	increased grip strength	Dram1<tm1.1(KOMP)Vlcg>/Dram1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dram1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262316	M	MP:0000598	abnormal liver morphology	Dram1<tm1.1(KOMP)Vlcg>/Dram1<tm1.1(KOMP)Vlcg>	C57BL/6N-Dram1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262317	F	MP:0002075	abnormal coat/hair pigmentation	Dram2<tm1b(EUCOMM)Wtsi>/Dram2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dram2<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6262318	F	MP:0005385	cardiovascular system phenotype	Drc7<em1(IMPC)J>/Drc7<em1(IMPC)J>	C57BL/6NJ-Drc7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262318	F	MP:0003929	decreased heart rate variability	Drc7<em1(IMPC)J>/Drc7<em1(IMPC)J>	C57BL/6NJ-Drc7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262318	M	MP:0001925	male infertility	Drc7<em1(IMPC)J>/Drc7<em1(IMPC)J>	C57BL/6NJ-Drc7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262318	F	MP:0004122	abnormal sinus arrhythmia	Drc7<em1(IMPC)J>/Drc7<em1(IMPC)J>	C57BL/6NJ-Drc7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262318	F	MP:0002968	increased circulating alkaline phosphatase level	Drc7<em1(IMPC)J>/Drc7<em1(IMPC)J>	C57BL/6NJ-Drc7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262319	M	MP:0005287	narrow eye opening	Dsc2<tm1e(KOMP)Wtsi>/Dsc2<tm1e(KOMP)Wtsi>	C57BL/6N-Dsc2<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262320	M	MP:0004924	abnormal behavior	Dsc3<tm1b(EUCOMM)Wtsi>/Dsc3<+>	C57BL/6N-Dsc3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262320	F	MP:0001333	absent optic nerve	Dsc3<tm1b(EUCOMM)Wtsi>/Dsc3<+>	C57BL/6N-Dsc3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262320	M	MP:0013278	decreased fasting circulating glucose level	Dsc3<tm1b(EUCOMM)Wtsi>/Dsc3<+>	C57BL/6N-Dsc3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262320	M	MP:0001399	hyperactivity	Dsc3<tm1b(EUCOMM)Wtsi>/Dsc3<+>	C57BL/6N-Dsc3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262320	M	MP:0020870	decreased thigmotaxis	Dsc3<tm1b(EUCOMM)Wtsi>/Dsc3<+>	C57BL/6N-Dsc3<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262322	M	MP:0005178	increased circulating cholesterol level	Dsg1c<em1(IMPC)Mbp>/Dsg1c<em1(IMPC)Mbp>	C57BL/6N-Dsg1c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262322	M	MP:0000194	increased circulating calcium level	Dsg1c<em1(IMPC)Mbp>/Dsg1c<em1(IMPC)Mbp>	C57BL/6N-Dsg1c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262322	M	MP:0002965	increased circulating serum albumin level	Dsg1c<em1(IMPC)Mbp>/Dsg1c<em1(IMPC)Mbp>	C57BL/6N-Dsg1c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262322	M	MP:0001402	decreased locomotor activity	Dsg1c<em1(IMPC)Mbp>/Dsg1c<em1(IMPC)Mbp>	C57BL/6N-Dsg1c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262322	M	MP:0001556	increased circulating HDL cholesterol level	Dsg1c<em1(IMPC)Mbp>/Dsg1c<em1(IMPC)Mbp>	C57BL/6N-Dsg1c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262323	F	MP:0009142	decreased prepulse inhibition	Dtx1<em1(IMPC)H>/Dtx1<em1(IMPC)H>	C57BL/6N-Dtx1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262323	M	MP:0005559	increased circulating glucose level	Dtx1<em1(IMPC)H>/Dtx1<em1(IMPC)H>	C57BL/6N-Dtx1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262323	M	MP:0005178	increased circulating cholesterol level	Dtx1<em1(IMPC)H>/Dtx1<em1(IMPC)H>	C57BL/6N-Dtx1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262325	F	MP:0010053	decreased grip strength	Dusp15<em1(IMPC)J>/Dusp15<em1(IMPC)J>	C57BL/6NJ-Dusp15<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262326	F	MP:0001258	decreased body length	Dusp16<em1(IMPC)Tcp>/Dusp16<em1(IMPC)Tcp>	C57BL/6NCrl-Dusp16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262326	M	MP:0000186	decreased circulating HDL cholesterol level	Dusp16<em1(IMPC)Tcp>/Dusp16<em1(IMPC)Tcp>	C57BL/6NCrl-Dusp16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262326	F	MP:0005561	increased mean corpuscular hemoglobin	Dusp16<em1(IMPC)Tcp>/Dusp16<em1(IMPC)Tcp>	C57BL/6NCrl-Dusp16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262326	F	MP:0000691	enlarged spleen	Dusp16<em1(IMPC)Tcp>/Dusp16<em1(IMPC)Tcp>	C57BL/6NCrl-Dusp16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262326	F	MP:0001120	abnormal uterus morphology	Dusp16<em1(IMPC)Tcp>/Dusp16<em1(IMPC)Tcp>	C57BL/6NCrl-Dusp16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262326	F	MP:0000702	enlarged lymph nodes	Dusp16<em1(IMPC)Tcp>/Dusp16<em1(IMPC)Tcp>	C57BL/6NCrl-Dusp16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262326	M	MP:0002833	increased heart weight	Dusp16<em1(IMPC)Tcp>/Dusp16<em1(IMPC)Tcp>	C57BL/6NCrl-Dusp16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262326	M	MP:0004952	increased spleen weight	Dusp16<em1(IMPC)Tcp>/Dusp16<em1(IMPC)Tcp>	C57BL/6NCrl-Dusp16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262326	M	MP:0002874	decreased hemoglobin content	Dusp16<em1(IMPC)Tcp>/Dusp16<em1(IMPC)Tcp>	C57BL/6NCrl-Dusp16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262326	M	MP:0005344	increased circulating bilirubin level	Dusp16<em1(IMPC)Tcp>/Dusp16<em1(IMPC)Tcp>	C57BL/6NCrl-Dusp16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262327	M	MP:0002110	abnormal digit morphology	Dusp18<em1(IMPC)J>/Dusp18<em1(IMPC)J>	C57BL/6NJ-Dusp18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262327	M	MP:0002833	increased heart weight	Dusp18<em1(IMPC)J>/Dusp18<em1(IMPC)J>	C57BL/6NJ-Dusp18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262327	F	MP:0001399	hyperactivity	Dusp18<em1(IMPC)J>/Dusp18<em1(IMPC)J>	C57BL/6NJ-Dusp18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262328	F	MP:0002339	abnormal lymph node morphology	Styxl2<em1(IMPC)Mbp>/Styxl2<em1(IMPC)Mbp>	C57BL/6N-Styxl2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262330	M	MP:0002060	abnormal skin morphology	Dync1li1<em1(IMPC)Tcp>/Dync1li1<+>	C57BL/6NCrl-Dync1li1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262330	F	MP:0002989	small kidney	Dync1li1<em1(IMPC)Tcp>/Dync1li1<+>	C57BL/6NCrl-Dync1li1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262330	F	MP:0002188	small heart	Dync1li1<em1(IMPC)Tcp>/Dync1li1<+>	C57BL/6NCrl-Dync1li1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262330	M	MP:0000157	abnormal sternum morphology	Dync1li1<em1(IMPC)Tcp>/Dync1li1<+>	C57BL/6NCrl-Dync1li1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262330	M	MP:0001146	abnormal testis morphology	Dync1li1<em1(IMPC)Tcp>/Dync1li1<+>	C57BL/6NCrl-Dync1li1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262330	F	MP:0000598	abnormal liver morphology	Dync1li1<em1(IMPC)Tcp>/Dync1li1<+>	C57BL/6NCrl-Dync1li1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262330	M	MP:0001175	abnormal lung morphology	Dync1li1<em1(IMPC)Tcp>/Dync1li1<+>	C57BL/6NCrl-Dync1li1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262330	M	MP:0004958	enlarged prostate gland	Dync1li1<em1(IMPC)Tcp>/Dync1li1<+>	C57BL/6NCrl-Dync1li1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262330	M	MP:0002059	abnormal seminal vesicle morphology	Dync1li1<em1(IMPC)Tcp>/Dync1li1<+>	C57BL/6NCrl-Dync1li1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262331	M	MP:0002059	abnormal seminal vesicle morphology	Dync1li1<em1(IMPC)Tcp>/Dync1li1<em1(IMPC)Tcp>	C57BL/6NCrl-Dync1li1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262331	M	MP:0002546	mydriasis	Dync1li1<em1(IMPC)Tcp>/Dync1li1<em1(IMPC)Tcp>	C57BL/6NCrl-Dync1li1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262336	M	MP:0000706	small thymus	Ecscr<tm1.1(KOMP)Vlcg>/Ecscr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ecscr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262336	M	MP:0002135	abnormal kidney morphology	Ecscr<tm1.1(KOMP)Vlcg>/Ecscr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ecscr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262336	M	MP:0004931	enlarged epididymis	Ecscr<tm1.1(KOMP)Vlcg>/Ecscr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ecscr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262336	M	MP:0002059	abnormal seminal vesicle morphology	Ecscr<tm1.1(KOMP)Vlcg>/Ecscr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ecscr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262336	M	MP:0000703	abnormal thymus morphology	Ecscr<tm1.1(KOMP)Vlcg>/Ecscr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ecscr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262336	M	MP:0002631	abnormal epididymis morphology	Ecscr<tm1.1(KOMP)Vlcg>/Ecscr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ecscr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262336	M	MP:0001157	small seminal vesicle	Ecscr<tm1.1(KOMP)Vlcg>/Ecscr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ecscr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262336	M	MP:0003068	enlarged kidney	Ecscr<tm1.1(KOMP)Vlcg>/Ecscr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ecscr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262336	M	MP:0000955	abnormal spinal cord morphology	Ecscr<tm1.1(KOMP)Vlcg>/Ecscr<tm1.1(KOMP)Vlcg>	C57BL/6N-Ecscr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262337	M	MP:0002599	increased mean platelet volume	Edc3<em1(IMPC)Tcp>/Edc3<em1(IMPC)Tcp>	C57BL/6NCrl-Edc3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262337	F	MP:0000702	enlarged lymph nodes	Edc3<em1(IMPC)Tcp>/Edc3<em1(IMPC)Tcp>	C57BL/6NCrl-Edc3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262337	F	MP:0003604	single kidney	Edc3<em1(IMPC)Tcp>/Edc3<em1(IMPC)Tcp>	C57BL/6NCrl-Edc3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262340	F	MP:0001523	impaired righting response	Eef1b2<em1(IMPC)J>/Eef1b2<em1(IMPC)J>	C57BL/6NJ-Eef1b2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262340	M	MP:0000062	increased bone mineral density	Eef1b2<em1(IMPC)J>/Eef1b2<em1(IMPC)J>	C57BL/6NJ-Eef1b2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262340	F	MP:0010124	decreased bone mineral content	Eef1b2<em1(IMPC)J>/Eef1b2<em1(IMPC)J>	C57BL/6NJ-Eef1b2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262340	M	MP:0010123	increased bone mineral content	Eef1b2<em1(IMPC)J>/Eef1b2<em1(IMPC)J>	C57BL/6NJ-Eef1b2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262340	F	MP:0000063	decreased bone mineral density	Eef1b2<em1(IMPC)J>/Eef1b2<em1(IMPC)J>	C57BL/6NJ-Eef1b2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262342	F	MP:0011110	preweaning lethality, incomplete penetrance	Efemp1<tm1.1(KOMP)Vlcg>/Efemp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Efemp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262342	M	MP:0000494	abnormal cecum morphology	Efemp1<tm1.1(KOMP)Vlcg>/Efemp1<tm1.1(KOMP)Vlcg>	C57BL/6N-Efemp1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262345	F	MP:0011471	decreased urine creatinine level	Efna4<tm1.1(KOMP)Vlcg>/Efna4<tm1.1(KOMP)Vlcg>	C57BL/6N-Efna4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262345	M	MP:0006243	impaired pupillary reflex	Efna4<tm1.1(KOMP)Vlcg>/Efna4<tm1.1(KOMP)Vlcg>	C57BL/6N-Efna4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262345	F	MP:0001312	abnormal cornea morphology	Efna4<tm1.1(KOMP)Vlcg>/Efna4<tm1.1(KOMP)Vlcg>	C57BL/6N-Efna4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262345	F	MP:0005560	decreased circulating glucose level	Efna4<tm1.1(KOMP)Vlcg>/Efna4<tm1.1(KOMP)Vlcg>	C57BL/6N-Efna4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262345	F	MP:0011396	abnormal sleep behavior	Efna4<tm1.1(KOMP)Vlcg>/Efna4<tm1.1(KOMP)Vlcg>	C57BL/6N-Efna4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262346	F	MP:0002591	decreased mean corpuscular volume	Egfem1<em1(IMPC)J>/Egfem1<em1(IMPC)J>	C57BL/6NJ-Egfem1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262346	F	MP:0001399	hyperactivity	Egfem1<em1(IMPC)J>/Egfem1<em1(IMPC)J>	C57BL/6NJ-Egfem1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262346	M	MP:0001486	abnormal startle reflex	Egfem1<em1(IMPC)J>/Egfem1<em1(IMPC)J>	C57BL/6NJ-Egfem1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262346	M	MP:0005293	impaired glucose tolerance	Egfem1<em1(IMPC)J>/Egfem1<em1(IMPC)J>	C57BL/6NJ-Egfem1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262346	M	MP:0013278	decreased fasting circulating glucose level	Egfem1<em1(IMPC)J>/Egfem1<em1(IMPC)J>	C57BL/6NJ-Egfem1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262346	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Egfem1<em1(IMPC)J>/Egfem1<em1(IMPC)J>	C57BL/6NJ-Egfem1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262346	M	MP:0002968	increased circulating alkaline phosphatase level	Egfem1<em1(IMPC)J>/Egfem1<em1(IMPC)J>	C57BL/6NJ-Egfem1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262348	M	MP:0005178	increased circulating cholesterol level	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6262348	M	MP:0000182	increased circulating LDL cholesterol level	Ehmt1<tm1b(EUCOMM)Hmgu>/Ehmt1<+>	C57BL/6N-Ehmt1<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6262351	F	MP:0001417	decreased exploration in new environment	Ehmt2<tm1.1(KOMP)Mbp>/Ehmt2<+>	C57BL/6N-Ehmt2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:6262351	M	MP:0001392	abnormal locomotor behavior	Ehmt2<tm1.1(KOMP)Mbp>/Ehmt2<+>	C57BL/6N-Ehmt2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:6262351	F	MP:0001399	hyperactivity	Ehmt2<tm1.1(KOMP)Mbp>/Ehmt2<+>	C57BL/6N-Ehmt2<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:6262352	F	MP:0001399	hyperactivity	Eid2<em1(IMPC)J>/Eid2<em1(IMPC)J>	C57BL/6NJ-Eid2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262352	M	MP:0002574	increased vertical activity	Eid2<em1(IMPC)J>/Eid2<em1(IMPC)J>	C57BL/6NJ-Eid2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262354	M	MP:0002599	increased mean platelet volume	Eif2a<em1(IMPC)Mbp>/Eif2a<em1(IMPC)Mbp>	C57BL/6N-Eif2a<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262354	F	MP:0000691	enlarged spleen	Eif2a<em1(IMPC)Mbp>/Eif2a<em1(IMPC)Mbp>	C57BL/6N-Eif2a<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262354	M	MP:0001415	increased exploration in new environment	Eif2a<em1(IMPC)Mbp>/Eif2a<em1(IMPC)Mbp>	C57BL/6N-Eif2a<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262354	F	MP:0000689	abnormal spleen morphology	Eif2a<em1(IMPC)Mbp>/Eif2a<em1(IMPC)Mbp>	C57BL/6N-Eif2a<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262354	M	MP:0002060	abnormal skin morphology	Eif2a<em1(IMPC)Mbp>/Eif2a<em1(IMPC)Mbp>	C57BL/6N-Eif2a<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262356	M	MP:0001147	small testis	Eif4enif1<em1(IMPC)Tcp>/Eif4enif1<+>	C57BL/6NCrl-Eif4enif1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262356	F	MP:0003020	decreased circulating chloride level	Eif4enif1<em1(IMPC)Tcp>/Eif4enif1<+>	C57BL/6NCrl-Eif4enif1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262357	M	MP:0000538	abnormal urinary bladder morphology	Eif4enif1<em1(IMPC)Tcp>/Eif4enif1<em1(IMPC)Tcp>	C57BL/6NCrl-Eif4enif1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262358	M	MP:0001914	hemorrhage	Eif4h<tm1b(EUCOMM)Wtsi>/Eif4h<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eif4h<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262359	F	MP:0002875	decreased erythrocyte cell number	Eipr1<em1(IMPC)J>/Eipr1<+>	C57BL/6NJ-Eipr1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262359	F	MP:0000208	decreased hematocrit	Eipr1<em1(IMPC)J>/Eipr1<+>	C57BL/6NJ-Eipr1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262361	M	MP:0006243	impaired pupillary reflex	Elavl1<tm1b(EUCOMM)Hmgu>/Elavl1<+>	C57BL/6N-Elavl1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262362	F	MP:0001697	abnormal embryo size	Elavl1<tm1b(EUCOMM)Hmgu>/Elavl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elavl1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262362	F	MP:0001785	edema	Elavl1<tm1b(EUCOMM)Hmgu>/Elavl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elavl1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262362	F	MP:0002109	abnormal limb morphology	Elavl1<tm1b(EUCOMM)Hmgu>/Elavl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elavl1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262362	F	MP:0001293	anophthalmia	Elavl1<tm1b(EUCOMM)Hmgu>/Elavl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Elavl1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262364	F	MP:0001399	hyperactivity	Elmod3<em1(IMPC)J>/Elmod3<em1(IMPC)J>	C57BL/6NJ-Elmod3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262366	M	MP:0000598	abnormal liver morphology	Emb<tm1b(KOMP)Wtsi>/Emb<+>	C57BL/6N-Emb<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262370	M	MP:0000208	decreased hematocrit	Emcn<em1(IMPC)Wtsi>/Emcn<em1(IMPC)Wtsi>	C57BL/6N-Emcn<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262370	M	MP:0005179	decreased circulating cholesterol level	Emcn<em1(IMPC)Wtsi>/Emcn<em1(IMPC)Wtsi>	C57BL/6N-Emcn<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262370	M	MP:0002875	decreased erythrocyte cell number	Emcn<em1(IMPC)Wtsi>/Emcn<em1(IMPC)Wtsi>	C57BL/6N-Emcn<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262370	M	MP:0000186	decreased circulating HDL cholesterol level	Emcn<em1(IMPC)Wtsi>/Emcn<em1(IMPC)Wtsi>	C57BL/6N-Emcn<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262370	M	MP:0002599	increased mean platelet volume	Emcn<em1(IMPC)Wtsi>/Emcn<em1(IMPC)Wtsi>	C57BL/6N-Emcn<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262370	M	MP:0002874	decreased hemoglobin content	Emcn<em1(IMPC)Wtsi>/Emcn<em1(IMPC)Wtsi>	C57BL/6N-Emcn<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262370	F	MP:0008806	increased circulating amylase level	Emcn<em1(IMPC)Wtsi>/Emcn<em1(IMPC)Wtsi>	C57BL/6N-Emcn<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262372	F	MP:0001399	hyperactivity	Emilin3<tm1.1(KOMP)Vlcg>/Emilin3<tm1.1(KOMP)Vlcg>	C57BL/6N-Emilin3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262372	M	MP:0002833	increased heart weight	Emilin3<tm1.1(KOMP)Vlcg>/Emilin3<tm1.1(KOMP)Vlcg>	C57BL/6N-Emilin3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262372	F	MP:0009142	decreased prepulse inhibition	Emilin3<tm1.1(KOMP)Vlcg>/Emilin3<tm1.1(KOMP)Vlcg>	C57BL/6N-Emilin3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262373	F	MP:0006358	absent pinna reflex	Eml1<em1(IMPC)Wtsi>/Eml1<em1(IMPC)Wtsi>	C57BL/6N-Eml1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262373	M	MP:0013278	decreased fasting circulating glucose level	Eml1<em1(IMPC)Wtsi>/Eml1<em1(IMPC)Wtsi>	C57BL/6N-Eml1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262373	M	MP:0002875	decreased erythrocyte cell number	Eml1<em1(IMPC)Wtsi>/Eml1<em1(IMPC)Wtsi>	C57BL/6N-Eml1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262373	M	MP:0005561	increased mean corpuscular hemoglobin	Eml1<em1(IMPC)Wtsi>/Eml1<em1(IMPC)Wtsi>	C57BL/6N-Eml1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262375	F	MP:0001102	small superior vagus ganglion	Enam<em1(IMPC)Tcp>/Enam<em1(IMPC)Tcp>	C57BL/6NCrl-Enam<em1(IMPC)Tcp>/TcpMmucd	N	MGI:5576271
MGI:6262375	F	MP:0000266	abnormal heart morphology	Enam<em1(IMPC)Tcp>/Enam<em1(IMPC)Tcp>	C57BL/6NCrl-Enam<em1(IMPC)Tcp>/TcpMmucd	N	MGI:5576271
MGI:6262375	F	MP:0009709	hydrometra	Enam<em1(IMPC)Tcp>/Enam<em1(IMPC)Tcp>	C57BL/6NCrl-Enam<em1(IMPC)Tcp>/TcpMmucd	N	MGI:5576271
MGI:6262375	F	MP:0000274	enlarged heart	Enam<em1(IMPC)Tcp>/Enam<em1(IMPC)Tcp>	C57BL/6NCrl-Enam<em1(IMPC)Tcp>/TcpMmucd	N	MGI:5576271
MGI:6262377	M	MP:0001488	increased startle reflex	Enpep<tm1b(KOMP)Wtsi>/Enpep<tm1b(KOMP)Wtsi>	C57BL/6N-Enpep<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262378	M	MP:0010025	decreased total body fat amount	Epb41l1<tm1b(EUCOMM)Wtsi>/Epb41l1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epb41l1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262378	F	MP:0013279	increased fasting circulating glucose level	Epb41l1<tm1b(EUCOMM)Wtsi>/Epb41l1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epb41l1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262378	F	MP:0001392	abnormal locomotor behavior	Epb41l1<tm1b(EUCOMM)Wtsi>/Epb41l1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epb41l1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262378	M	MP:0005292	improved glucose tolerance	Epb41l1<tm1b(EUCOMM)Wtsi>/Epb41l1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epb41l1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262378	M	MP:0001340	abnormal eyelid morphology	Epb41l1<tm1b(EUCOMM)Wtsi>/Epb41l1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epb41l1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262378	M	MP:0010053	decreased grip strength	Epb41l1<tm1b(EUCOMM)Wtsi>/Epb41l1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epb41l1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262378	M	MP:0003960	increased lean body mass	Epb41l1<tm1b(EUCOMM)Wtsi>/Epb41l1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epb41l1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262378	M	MP:0005343	increased circulating aspartate transaminase level	Epb41l1<tm1b(EUCOMM)Wtsi>/Epb41l1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epb41l1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262378	F	MP:0020870	decreased thigmotaxis	Epb41l1<tm1b(EUCOMM)Wtsi>/Epb41l1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epb41l1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262378	M	MP:0001488	increased startle reflex	Epb41l1<tm1b(EUCOMM)Wtsi>/Epb41l1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epb41l1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262378	M	MP:0012121	sclerocornea	Epb41l1<tm1b(EUCOMM)Wtsi>/Epb41l1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epb41l1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262378	M	MP:0005102	abnormal iris pigmentation	Epb41l1<tm1b(EUCOMM)Wtsi>/Epb41l1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epb41l1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262378	M	MP:0010123	increased bone mineral content	Epb41l1<tm1b(EUCOMM)Wtsi>/Epb41l1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epb41l1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262379	M	MP:0009142	decreased prepulse inhibition	Epha5<tm1b(NCOM)Mfgc>/Epha5<tm1b(NCOM)Mfgc>	C57BL/6N-Epha5<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:6262379	M	MP:0013279	increased fasting circulating glucose level	Epha5<tm1b(NCOM)Mfgc>/Epha5<tm1b(NCOM)Mfgc>	C57BL/6N-Epha5<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:6262380	F	MP:0009456	impaired cued conditioning behavior	Eps8l2<tm1b(EUCOMM)Wtsi>/Eps8l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eps8l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262380	F	MP:0005344	increased circulating bilirubin level	Eps8l2<tm1b(EUCOMM)Wtsi>/Eps8l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eps8l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262380	M	MP:0002102	abnormal ear morphology	Eps8l2<tm1b(EUCOMM)Wtsi>/Eps8l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eps8l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262380	M	MP:0002968	increased circulating alkaline phosphatase level	Eps8l2<tm1b(EUCOMM)Wtsi>/Eps8l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eps8l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262380	F	MP:0005419	decreased circulating serum albumin level	Eps8l2<tm1b(EUCOMM)Wtsi>/Eps8l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eps8l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262380	F	MP:0000195	decreased circulating calcium level	Eps8l2<tm1b(EUCOMM)Wtsi>/Eps8l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eps8l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262380	M	MP:0000443	abnormal snout morphology	Eps8l2<tm1b(EUCOMM)Wtsi>/Eps8l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eps8l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262380	M	MP:0001489	decreased startle reflex	Eps8l2<tm1b(EUCOMM)Wtsi>/Eps8l2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eps8l2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262381	M	MP:0000220	increased monocyte cell number	Epx<tm1b(EUCOMM)Wtsi>/Epx<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epx<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262381	M	MP:0001552	increased circulating triglyceride level	Epx<tm1b(EUCOMM)Wtsi>/Epx<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epx<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262381	M	MP:0010024	increased total body fat amount	Epx<tm1b(EUCOMM)Wtsi>/Epx<tm1b(EUCOMM)Wtsi>	C57BL/6N-Epx<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262384	F	MP:0009709	hydrometra	Erf<tm1.1(KOMP)Mbp>/Erf<+>	C57BL/6N-Erf<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262384	F	MP:0001120	abnormal uterus morphology	Erf<tm1.1(KOMP)Mbp>/Erf<+>	C57BL/6N-Erf<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262384	M	MP:0002100	abnormal tooth morphology	Erf<tm1.1(KOMP)Mbp>/Erf<+>	C57BL/6N-Erf<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262384	M	MP:0009552	urinary bladder obstruction	Erf<tm1.1(KOMP)Mbp>/Erf<+>	C57BL/6N-Erf<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262384	M	MP:0000266	abnormal heart morphology	Erf<tm1.1(KOMP)Mbp>/Erf<+>	C57BL/6N-Erf<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262384	M	MP:0000274	enlarged heart	Erf<tm1.1(KOMP)Mbp>/Erf<+>	C57BL/6N-Erf<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262387	F	MP:0002339	abnormal lymph node morphology	Erlec1<em1(IMPC)Mbp>/Erlec1<em1(IMPC)Mbp>	C57BL/6N-Erlec1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262387	F	MP:0000702	enlarged lymph nodes	Erlec1<em1(IMPC)Mbp>/Erlec1<em1(IMPC)Mbp>	C57BL/6N-Erlec1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262387	F	MP:0010025	decreased total body fat amount	Erlec1<em1(IMPC)Mbp>/Erlec1<em1(IMPC)Mbp>	C57BL/6N-Erlec1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262390	M	MP:0002135	abnormal kidney morphology	Evi2b<tm1.1(KOMP)Vlcg>/Evi2b<tm1.1(KOMP)Vlcg>	C57BL/6N-Evi2b<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262390	M	MP:0003068	enlarged kidney	Evi2b<tm1.1(KOMP)Vlcg>/Evi2b<tm1.1(KOMP)Vlcg>	C57BL/6N-Evi2b<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262391	M	MP:0005562	decreased mean corpuscular hemoglobin	Exd1<tm1b(EUCOMM)Hmgu>/Exd1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Exd1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6262391	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Exd1<tm1b(EUCOMM)Hmgu>/Exd1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Exd1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6262393	M	MP:0013278	decreased fasting circulating glucose level	Exoc3<tm2b(EUCOMM)Hmgu>/Exoc3<+>	C57BL/6N-Exoc3<tm2b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6262393	M	MP:0010025	decreased total body fat amount	Exoc3<tm2b(EUCOMM)Hmgu>/Exoc3<+>	C57BL/6N-Exoc3<tm2b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6262393	M	MP:0003960	increased lean body mass	Exoc3<tm2b(EUCOMM)Hmgu>/Exoc3<+>	C57BL/6N-Exoc3<tm2b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6262394	M	MP:0001399	hyperactivity	Exoc6<tm1b(EUCOMM)Wtsi>/Exoc6<+>	C57BL/6N-Exoc6<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262397	F	MP:0005628	decreased circulating potassium level	Exph5<tm1b(EUCOMM)Wtsi>/Exph5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Exph5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262397	M	MP:0001364	decreased anxiety-related response	Exph5<tm1b(EUCOMM)Wtsi>/Exph5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Exph5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262397	M	MP:0004924	abnormal behavior	Exph5<tm1b(EUCOMM)Wtsi>/Exph5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Exph5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262397	F	MP:0000198	decreased circulating phosphate level	Exph5<tm1b(EUCOMM)Wtsi>/Exph5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Exph5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262397	M	MP:0020870	decreased thigmotaxis	Exph5<tm1b(EUCOMM)Wtsi>/Exph5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Exph5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262400	M	MP:0001488	increased startle reflex	F2rl1<tm1b(EUCOMM)Wtsi>/F2rl1<tm1b(EUCOMM)Wtsi>	C57BL/6N-F2rl1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262402	F	MP:0002151	abnormal neural tube morphology	Faf2<em1(IMPC)Mbp>/Faf2<+>	C57BL/6N-Faf2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262402	F	MP:0001297	microphthalmia	Faf2<em1(IMPC)Mbp>/Faf2<+>	C57BL/6N-Faf2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262402	F	MP:0003984	embryonic growth retardation	Faf2<em1(IMPC)Mbp>/Faf2<+>	C57BL/6N-Faf2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262403	M	MP:0005344	increased circulating bilirubin level	Fam114a1<em1(IMPC)J>/Fam114a1<em1(IMPC)J>	C57BL/6NJ-Fam114a1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262404	F	MP:0002968	increased circulating alkaline phosphatase level	Fam120a<em1(IMPC)J>/Fam120a<em1(IMPC)J>	C57BL/6NJ-Fam120a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262404	M	MP:0002833	increased heart weight	Fam120a<em1(IMPC)J>/Fam120a<em1(IMPC)J>	C57BL/6NJ-Fam120a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262404	M	MP:0003960	increased lean body mass	Fam120a<em1(IMPC)J>/Fam120a<em1(IMPC)J>	C57BL/6NJ-Fam120a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262404	M	MP:0010123	increased bone mineral content	Fam120a<em1(IMPC)J>/Fam120a<em1(IMPC)J>	C57BL/6NJ-Fam120a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262404	M	MP:0000062	increased bone mineral density	Fam120a<em1(IMPC)J>/Fam120a<em1(IMPC)J>	C57BL/6NJ-Fam120a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262404	M	MP:0001415	increased exploration in new environment	Fam120a<em1(IMPC)J>/Fam120a<em1(IMPC)J>	C57BL/6NJ-Fam120a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262404	M	MP:0010025	decreased total body fat amount	Fam120a<em1(IMPC)J>/Fam120a<em1(IMPC)J>	C57BL/6NJ-Fam120a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262406	M	MP:0001303	abnormal lens morphology	Fam162a<tm1b(EUCOMM)Hmgu>/Fam162a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fam162a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262406	M	MP:0001304	cataract	Fam162a<tm1b(EUCOMM)Hmgu>/Fam162a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fam162a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262406	M	MP:0002699	abnormal vitreous body morphology	Fam162a<tm1b(EUCOMM)Hmgu>/Fam162a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fam162a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262406	M	MP:0001325	abnormal retina morphology	Fam162a<tm1b(EUCOMM)Hmgu>/Fam162a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fam162a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262407	M	MP:0005292	improved glucose tolerance	Fam163a<tm2b(KOMP)Wtsi>/Fam163a<tm2b(KOMP)Wtsi>	C57BL/6N-Fam163a<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262407	F	MP:0000218	increased leukocyte cell number	Fam163a<tm2b(KOMP)Wtsi>/Fam163a<tm2b(KOMP)Wtsi>	C57BL/6N-Fam163a<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262407	F	MP:0002968	increased circulating alkaline phosphatase level	Fam163a<tm2b(KOMP)Wtsi>/Fam163a<tm2b(KOMP)Wtsi>	C57BL/6N-Fam163a<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262407	F	MP:0002546	mydriasis	Fam163a<tm2b(KOMP)Wtsi>/Fam163a<tm2b(KOMP)Wtsi>	C57BL/6N-Fam163a<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262407	M	MP:0005568	increased circulating total protein level	Fam163a<tm2b(KOMP)Wtsi>/Fam163a<tm2b(KOMP)Wtsi>	C57BL/6N-Fam163a<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262407	M	MP:0001258	decreased body length	Fam163a<tm2b(KOMP)Wtsi>/Fam163a<tm2b(KOMP)Wtsi>	C57BL/6N-Fam163a<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262408	M	MP:0002606	increased basophil cell number	Cimip2b<tm1(KOMP)Wtsi>/Cimip2b<tm1(KOMP)Wtsi>	C57BL/6N-Cimip2b<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262408	M	MP:0005011	increased eosinophil cell number	Cimip2b<tm1(KOMP)Wtsi>/Cimip2b<tm1(KOMP)Wtsi>	C57BL/6N-Cimip2b<tm1(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262409	M	MP:0001925	male infertility	Fam170a<em1(IMPC)Tcp>/Fam170a<em1(IMPC)Tcp>	C57BL/6NCrl-Fam170a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262410	F	MP:0005343	increased circulating aspartate transaminase level	Antkmt<tm1.1(KOMP)Vlcg>/Antkmt<tm1.1(KOMP)Vlcg>	C57BL/6N-Antkmt<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262410	F	MP:0009709	hydrometra	Antkmt<tm1.1(KOMP)Vlcg>/Antkmt<tm1.1(KOMP)Vlcg>	C57BL/6N-Antkmt<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262410	F	MP:0002941	increased circulating alanine transaminase level	Antkmt<tm1.1(KOMP)Vlcg>/Antkmt<tm1.1(KOMP)Vlcg>	C57BL/6N-Antkmt<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262410	F	MP:0001120	abnormal uterus morphology	Antkmt<tm1.1(KOMP)Vlcg>/Antkmt<tm1.1(KOMP)Vlcg>	C57BL/6N-Antkmt<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262411	M	MP:0000194	increased circulating calcium level	Fam184b<tm2b(EUCOMM)Wtsi>/Fam184b<tm2b(EUCOMM)Wtsi>	C57BL/6N-Fam184b<tm2b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262411	M	MP:0005559	increased circulating glucose level	Fam184b<tm2b(EUCOMM)Wtsi>/Fam184b<tm2b(EUCOMM)Wtsi>	C57BL/6N-Fam184b<tm2b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262412	F	MP:0002574	increased vertical activity	Tafa1<tm1.1(KOMP)Vlcg>/Tafa1<tm1.1(KOMP)Vlcg>	C57BL/6N-Tafa1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262414	M	MP:0001304	cataract	Fam216a<tm1b(EUCOMM)Hmgu>/Fam216a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fam216a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262414	M	MP:0001303	abnormal lens morphology	Fam216a<tm1b(EUCOMM)Hmgu>/Fam216a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fam216a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262415	M	MP:0002135	abnormal kidney morphology	Fam72a<tm1.1(KOMP)Vlcg>/Fam72a<tm1.1(KOMP)Vlcg>	C57BL/6N-Fam72a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262415	M	MP:0008528	polycystic kidney	Fam72a<tm1.1(KOMP)Vlcg>/Fam72a<tm1.1(KOMP)Vlcg>	C57BL/6N-Fam72a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262416	M	MP:0010123	increased bone mineral content	Far1<em1(IMPC)Wtsi>/Far1<+>	C57BL/6N-Far1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262416	M	MP:0000062	increased bone mineral density	Far1<em1(IMPC)Wtsi>/Far1<+>	C57BL/6N-Far1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262417	M	MP:0005343	increased circulating aspartate transaminase level	Fars2<em1(IMPC)J>/Fars2<+>	C57BL/6NJ-Fars2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262423	M	MP:0001513	limb grasping	Fbxl21<tm2b(EUCOMM)Wtsi>/Fbxl21<tm2b(EUCOMM)Wtsi>	C57BL/6N-Fbxl21<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262424	F	MP:0000208	decreased hematocrit	Fbxo10<tm1b(KOMP)Wtsi>/Fbxo10<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo10<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262424	M	MP:0002644	decreased circulating triglyceride level	Fbxo10<tm1b(KOMP)Wtsi>/Fbxo10<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo10<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262424	F	MP:0002591	decreased mean corpuscular volume	Fbxo10<tm1b(KOMP)Wtsi>/Fbxo10<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo10<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262424	M	MP:0005560	decreased circulating glucose level	Fbxo10<tm1b(KOMP)Wtsi>/Fbxo10<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo10<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262424	F	MP:0000198	decreased circulating phosphate level	Fbxo10<tm1b(KOMP)Wtsi>/Fbxo10<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo10<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262424	F	MP:0005140	decreased cardiac muscle contractility	Fbxo10<tm1b(KOMP)Wtsi>/Fbxo10<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo10<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262424	F	MP:0000195	decreased circulating calcium level	Fbxo10<tm1b(KOMP)Wtsi>/Fbxo10<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxo10<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262427	M	MP:0010097	abnormal retina blood vessel morphology	Fbxw17<tm1b(KOMP)Wtsi>/Fbxw17<tm1b(KOMP)Wtsi>	C57BL/6N-Fbxw17<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262428	F	MP:0002606	increased basophil cell number	Fbxw2<tm1b(EUCOMM)Hmgu>/Fbxw2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fbxw2<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:6262429	M	MP:0002059	abnormal seminal vesicle morphology	Fcgbp<tm1b(EUCOMM)Wtsi>/Fcgbp<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fcgbp<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:6262429	M	MP:0002092	abnormal eye morphology	Fcgbp<tm1b(EUCOMM)Wtsi>/Fcgbp<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fcgbp<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:6262429	F	MP:0002968	increased circulating alkaline phosphatase level	Fcgbp<tm1b(EUCOMM)Wtsi>/Fcgbp<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fcgbp<tm1b(EUCOMM)Wtsi>/Cnrm	N	MGI:5576271
MGI:6262430	F	MP:0001406	abnormal gait	Fcgr3<tm1b(EUCOMM)Hmgu>/Fcgr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fcgr3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262430	M	MP:0002626	increased heart rate	Fcgr3<tm1b(EUCOMM)Hmgu>/Fcgr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fcgr3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262430	F	MP:0000745	tremors	Fcgr3<tm1b(EUCOMM)Hmgu>/Fcgr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fcgr3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262430	M	MP:0003233	prolonged QT interval	Fcgr3<tm1b(EUCOMM)Hmgu>/Fcgr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fcgr3<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262431	F	MP:0005562	decreased mean corpuscular hemoglobin	Fcho2<tm1b(EUCOMM)Hmgu>/Fcho2<+>	C57BL/6N-Fcho2<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6262431	F	MP:0010067	increased red blood cell distribution width	Fcho2<tm1b(EUCOMM)Hmgu>/Fcho2<+>	C57BL/6N-Fcho2<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6262433	F	MP:0009142	decreased prepulse inhibition	Fcmr<tm1b(KOMP)Wtsi>/Fcmr<tm1b(KOMP)Wtsi>	C57BL/6N-Fcmr<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262433	F	MP:0000642	enlarged adrenal glands	Fcmr<tm1b(KOMP)Wtsi>/Fcmr<tm1b(KOMP)Wtsi>	C57BL/6N-Fcmr<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262435	M	MP:0001284	absent vibrissae	Fer1l4<tm1b(EUCOMM)Hmgu>/Fer1l4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fer1l4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262437	F	MP:0000198	decreased circulating phosphate level	Fgb<tm1.1(KOMP)Vlcg>/Fgb<+>	C57BL/6N-Fgb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262438	M	MP:0001297	microphthalmia	Fgd1<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Fgd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262438	M	MP:0001697	abnormal embryo size	Fgd1<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Fgd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262438	M	MP:0003984	embryonic growth retardation	Fgd1<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Fgd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262438	M	MP:0001785	edema	Fgd1<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Fgd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262438	M	MP:0000428	abnormal craniofacial morphology	Fgd1<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Fgd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262439	M	MP:0000182	increased circulating LDL cholesterol level	Fgd4<tm1a(EUCOMM)Wtsi>/Fgd4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Fgd4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262440	M	MP:0008806	increased circulating amylase level	Fgf22<tm1b(EUCOMM)Hmgu>/Fgf22<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fgf22<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262440	M	MP:0001406	abnormal gait	Fgf22<tm1b(EUCOMM)Hmgu>/Fgf22<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fgf22<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262441	M	MP:0000219	increased neutrophil cell number	Fgfbp3<tm1.1(KOMP)Wtsi>/Fgfbp3<tm1.1(KOMP)Wtsi>	C57BL/6N-Fgfbp3<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262442	F	MP:0000452	abnormal mouth morphology	Ficd<tm1b(EUCOMM)Hmgu>/Ficd<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ficd<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262442	F	MP:0005565	increased blood urea nitrogen level	Ficd<tm1b(EUCOMM)Hmgu>/Ficd<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ficd<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262442	F	MP:0001284	absent vibrissae	Ficd<tm1b(EUCOMM)Hmgu>/Ficd<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ficd<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262446	F	MP:0001513	limb grasping	Fkbp6<tm1b(KOMP)Wtsi>/Fkbp6<tm1b(KOMP)Wtsi>	C57BL/6N-Fkbp6<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262446	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Fkbp6<tm1b(KOMP)Wtsi>/Fkbp6<tm1b(KOMP)Wtsi>	C57BL/6N-Fkbp6<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262450	F	MP:0002764	short tibia	Fmnl2<em2(IMPC)Tcp>/Fmnl2<em2(IMPC)Tcp>	C57BL/6NCrl-Fmnl2<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262450	F	MP:0005278	abnormal cholesterol homeostasis	Fmnl2<em2(IMPC)Tcp>/Fmnl2<em2(IMPC)Tcp>	C57BL/6NCrl-Fmnl2<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262451	F	MP:0001513	limb grasping	Fndc4<tm1.1(KOMP)Vlcg>/Fndc4<tm1.1(KOMP)Vlcg>	C57BL/6N-Fndc4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262452	M	MP:0001925	male infertility	Fndc9<tm1.1(KOMP)Vlcg>/Fndc9<tm1.1(KOMP)Vlcg>	C57BL/6N-Fndc9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262452	F	MP:0020870	decreased thigmotaxis	Fndc9<tm1.1(KOMP)Vlcg>/Fndc9<tm1.1(KOMP)Vlcg>	C57BL/6N-Fndc9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262452	F	MP:0009142	decreased prepulse inhibition	Fndc9<tm1.1(KOMP)Vlcg>/Fndc9<tm1.1(KOMP)Vlcg>	C57BL/6N-Fndc9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262452	F	MP:0001926	female infertility	Fndc9<tm1.1(KOMP)Vlcg>/Fndc9<tm1.1(KOMP)Vlcg>	C57BL/6N-Fndc9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262452	F	MP:0005016	decreased lymphocyte cell number	Fndc9<tm1.1(KOMP)Vlcg>/Fndc9<tm1.1(KOMP)Vlcg>	C57BL/6N-Fndc9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262452	F	MP:0005344	increased circulating bilirubin level	Fndc9<tm1.1(KOMP)Vlcg>/Fndc9<tm1.1(KOMP)Vlcg>	C57BL/6N-Fndc9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262452	F	MP:0000219	increased neutrophil cell number	Fndc9<tm1.1(KOMP)Vlcg>/Fndc9<tm1.1(KOMP)Vlcg>	C57BL/6N-Fndc9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262452	M	MP:0002968	increased circulating alkaline phosphatase level	Fndc9<tm1.1(KOMP)Vlcg>/Fndc9<tm1.1(KOMP)Vlcg>	C57BL/6N-Fndc9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262452	M	MP:0010053	decreased grip strength	Fndc9<tm1.1(KOMP)Vlcg>/Fndc9<tm1.1(KOMP)Vlcg>	C57BL/6N-Fndc9<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262454	M	MP:0002060	abnormal skin morphology	Fosb<tm1b(KOMP)Wtsi>/Fosb<tm1b(KOMP)Wtsi>	C57BL/6N-Fosb<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262454	M	MP:0003068	enlarged kidney	Fosb<tm1b(KOMP)Wtsi>/Fosb<tm1b(KOMP)Wtsi>	C57BL/6N-Fosb<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262454	M	MP:0000063	decreased bone mineral density	Fosb<tm1b(KOMP)Wtsi>/Fosb<tm1b(KOMP)Wtsi>	C57BL/6N-Fosb<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262454	M	MP:0002135	abnormal kidney morphology	Fosb<tm1b(KOMP)Wtsi>/Fosb<tm1b(KOMP)Wtsi>	C57BL/6N-Fosb<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262455	F	MP:0010124	decreased bone mineral content	Foxk2<em1(IMPC)J>/Foxk2<em1(IMPC)J>	C57BL/6NJ-Foxk2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262455	F	MP:0000063	decreased bone mineral density	Foxk2<em1(IMPC)J>/Foxk2<em1(IMPC)J>	C57BL/6NJ-Foxk2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262455	F	MP:0003795	abnormal bone structure	Foxk2<em1(IMPC)J>/Foxk2<em1(IMPC)J>	C57BL/6NJ-Foxk2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262455	F	MP:0010097	abnormal retina blood vessel morphology	Foxk2<em1(IMPC)J>/Foxk2<em1(IMPC)J>	C57BL/6NJ-Foxk2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262456	F	MP:0001102	small superior vagus ganglion	Foxn1<tm1.1(KOMP)Vlcg>/Foxn1<+>	C57BL/6N-Foxn1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262456	F	MP:0009709	hydrometra	Foxn1<tm1.1(KOMP)Vlcg>/Foxn1<+>	C57BL/6N-Foxn1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262458	F	MP:0001399	hyperactivity	Foxo1<tm1b(EUCOMM)Wtsi>/Foxo1<+>	C57BL/6N-Foxo1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262458	M	MP:0005344	increased circulating bilirubin level	Foxo1<tm1b(EUCOMM)Wtsi>/Foxo1<+>	C57BL/6N-Foxo1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262458	F	MP:0002590	increased mean corpuscular volume	Foxo1<tm1b(EUCOMM)Wtsi>/Foxo1<+>	C57BL/6N-Foxo1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262458	M	MP:0005655	increased aggression	Foxo1<tm1b(EUCOMM)Wtsi>/Foxo1<+>	C57BL/6N-Foxo1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262460	M	MP:0000274	enlarged heart	Foxo4<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Foxo4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262460	M	MP:0000538	abnormal urinary bladder morphology	Foxo4<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Foxo4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262460	M	MP:0000266	abnormal heart morphology	Foxo4<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Foxo4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262461	F	MP:0003960	increased lean body mass	Foxp1<tm1b(KOMP)Wtsi>/Foxp1<+>	C57BL/6N-Foxp1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262463	F	MP:0000689	abnormal spleen morphology	Foxr1<em1(IMPC)Tcp>/Foxr1<em1(IMPC)Tcp>	C57BL/6NCrl-Foxr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262463	M	MP:0000702	enlarged lymph nodes	Foxr1<em1(IMPC)Tcp>/Foxr1<em1(IMPC)Tcp>	C57BL/6NCrl-Foxr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262464	M	MP:0001529	abnormal vocalization	Frmd6<em1(IMPC)H>/Frmd6<+>	C57BL/6NTac-Frmd6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262464	M	MP:0005655	increased aggression	Frmd6<em1(IMPC)H>/Frmd6<+>	C57BL/6NTac-Frmd6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262465	F	MP:0005287	narrow eye opening	Frmd6<em1(IMPC)H>/Frmd6<em1(IMPC)H>	C57BL/6NTac-Frmd6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262465	F	MP:0002833	increased heart weight	Frmd6<em1(IMPC)H>/Frmd6<em1(IMPC)H>	C57BL/6NTac-Frmd6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262465	M	MP:0001406	abnormal gait	Frmd6<em1(IMPC)H>/Frmd6<em1(IMPC)H>	C57BL/6NTac-Frmd6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262465	F	MP:0001402	decreased locomotor activity	Frmd6<em1(IMPC)H>/Frmd6<em1(IMPC)H>	C57BL/6NTac-Frmd6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262466	M	MP:0005561	increased mean corpuscular hemoglobin	Fryl<tm1b(KOMP)Wtsi>/Fryl<+>	C57BL/6N-Fryl<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262467	F	MP:0000702	enlarged lymph nodes	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	F	MP:0001297	microphthalmia	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	F	MP:0000689	abnormal spleen morphology	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	M	MP:0002833	increased heart weight	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	F	MP:0000691	enlarged spleen	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	F	MP:0001120	abnormal uterus morphology	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	F	MP:0010507	shortened RR interval	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	M	MP:0010052	increased grip strength	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	F	MP:0001126	abnormal ovary morphology	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	F	MP:0002626	increased heart rate	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	F	MP:0001314	cornea opacity	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	F	MP:0002092	abnormal eye morphology	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	M	MP:0003642	absent seminal vesicle	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	M	MP:0002997	enlarged seminal vesicle	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	F	MP:0004832	enlarged ovary	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	M	MP:0000198	decreased circulating phosphate level	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	F	MP:0002989	small kidney	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	F	MP:0002339	abnormal lymph node morphology	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262467	F	MP:0002135	abnormal kidney morphology	Fsd2<em1(IMPC)Mbp>/Fsd2<em1(IMPC)Mbp>	C57BL/6N-Fsd2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262468	M	MP:0002092	abnormal eye morphology	Fth1<tm1.1(KOMP)Vlcg>/Fth1<+>	C57BL/6N-Fth1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262472	M	MP:0000063	decreased bone mineral density	Fundc1<tm1c(KOMP)Wtsi>/Y	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Fundc1<tm1c(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262472	M	MP:0002834	decreased heart weight	Fundc1<tm1c(KOMP)Wtsi>/Y	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Fundc1<tm1c(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262474	M	MP:0002059	abnormal seminal vesicle morphology	Fut1<tm1b(KOMP)Wtsi>/Fut1<tm1b(KOMP)Wtsi>	C57BL/6N-Fut1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262474	M	MP:0002691	small stomach	Fut1<tm1b(KOMP)Wtsi>/Fut1<tm1b(KOMP)Wtsi>	C57BL/6N-Fut1<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262477	F	MP:0011110	preweaning lethality, incomplete penetrance	Fxyd7<tm1b(KOMP)Wtsi>/Fxyd7<tm1b(KOMP)Wtsi>	C57BL/6N-Fxyd7<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262479	M	MP:0000274	enlarged heart	Fzd5<tm1.1(KOMP)Vlcg>/Fzd5<+>	C57BL/6N-Fzd5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262479	F	MP:0001102	small superior vagus ganglion	Fzd5<tm1.1(KOMP)Vlcg>/Fzd5<+>	C57BL/6N-Fzd5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262479	F	MP:0009709	hydrometra	Fzd5<tm1.1(KOMP)Vlcg>/Fzd5<+>	C57BL/6N-Fzd5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262479	M	MP:0000266	abnormal heart morphology	Fzd5<tm1.1(KOMP)Vlcg>/Fzd5<+>	C57BL/6N-Fzd5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262481	M	MP:0000274	enlarged heart	Fzr1<tm1.1(KOMP)Vlcg>/Fzr1<+>	C57BL/6N-Fzr1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262481	M	MP:0000266	abnormal heart morphology	Fzr1<tm1.1(KOMP)Vlcg>/Fzr1<+>	C57BL/6N-Fzr1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262482	F	MP:0001944	abnormal pancreas morphology	G2e3<em1(IMPC)Tcp>/G2e3<em1(IMPC)Tcp>	C57BL/6NCrl-G2e3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262482	F	MP:0002060	abnormal skin morphology	G2e3<em1(IMPC)Tcp>/G2e3<em1(IMPC)Tcp>	C57BL/6NCrl-G2e3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262482	F	MP:0002637	small uterus	G2e3<em1(IMPC)Tcp>/G2e3<em1(IMPC)Tcp>	C57BL/6NCrl-G2e3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262482	F	MP:0010124	decreased bone mineral content	G2e3<em1(IMPC)Tcp>/G2e3<em1(IMPC)Tcp>	C57BL/6NCrl-G2e3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262482	F	MP:0002989	small kidney	G2e3<em1(IMPC)Tcp>/G2e3<em1(IMPC)Tcp>	C57BL/6NCrl-G2e3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262482	M	MP:0009456	impaired cued conditioning behavior	G2e3<em1(IMPC)Tcp>/G2e3<em1(IMPC)Tcp>	C57BL/6NCrl-G2e3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262482	F	MP:0000627	abnormal mammary gland morphology	G2e3<em1(IMPC)Tcp>/G2e3<em1(IMPC)Tcp>	C57BL/6NCrl-G2e3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262482	F	MP:0000689	abnormal spleen morphology	G2e3<em1(IMPC)Tcp>/G2e3<em1(IMPC)Tcp>	C57BL/6NCrl-G2e3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262482	F	MP:0000063	decreased bone mineral density	G2e3<em1(IMPC)Tcp>/G2e3<em1(IMPC)Tcp>	C57BL/6NCrl-G2e3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262482	F	MP:0002188	small heart	G2e3<em1(IMPC)Tcp>/G2e3<em1(IMPC)Tcp>	C57BL/6NCrl-G2e3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262482	F	MP:0001258	decreased body length	G2e3<em1(IMPC)Tcp>/G2e3<em1(IMPC)Tcp>	C57BL/6NCrl-G2e3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262482	F	MP:0005343	increased circulating aspartate transaminase level	G2e3<em1(IMPC)Tcp>/G2e3<em1(IMPC)Tcp>	C57BL/6NCrl-G2e3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262483	F	MP:0011965	decreased total retina thickness	G3bp1<tm1b(KOMP)Wtsi>/G3bp1<tm1b(KOMP)Wtsi>	C57BL/6N-G3bp1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262483	M	MP:0009142	decreased prepulse inhibition	G3bp1<tm1b(KOMP)Wtsi>/G3bp1<tm1b(KOMP)Wtsi>	C57BL/6N-G3bp1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262483	F	MP:0001325	abnormal retina morphology	G3bp1<tm1b(KOMP)Wtsi>/G3bp1<tm1b(KOMP)Wtsi>	C57BL/6N-G3bp1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262484	M	MP:0000702	enlarged lymph nodes	G6pd2<em1(IMPC)Tcp>/G6pd2<em1(IMPC)Tcp>	C57BL/6NCrl-G6pd2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262486	M	MP:0003743	abnormal facial morphology	Gabpa<em2(IMPC)Mbp>/Gabpa<em2(IMPC)Mbp>	C57BL/6N-Gabpa<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262486	M	MP:0000438	abnormal cranium morphology	Gabpa<em2(IMPC)Mbp>/Gabpa<em2(IMPC)Mbp>	C57BL/6N-Gabpa<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262486	M	MP:0002102	abnormal ear morphology	Gabpa<em2(IMPC)Mbp>/Gabpa<em2(IMPC)Mbp>	C57BL/6N-Gabpa<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262487	M	MP:0003961	decreased lean body mass	Gabrg3<em1(IMPC)J>/Gabrg3<em1(IMPC)J>	C57BL/6NJ-Gabrg3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262487	M	MP:0010124	decreased bone mineral content	Gabrg3<em1(IMPC)J>/Gabrg3<em1(IMPC)J>	C57BL/6NJ-Gabrg3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262487	M	MP:0010024	increased total body fat amount	Gabrg3<em1(IMPC)J>/Gabrg3<em1(IMPC)J>	C57BL/6NJ-Gabrg3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262491	F	MP:0000689	abnormal spleen morphology	Gapvd1<em1(IMPC)Mbp>/Gapvd1<+>	C57BL/6N-Gapvd1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262491	F	MP:0002188	small heart	Gapvd1<em1(IMPC)Mbp>/Gapvd1<+>	C57BL/6N-Gapvd1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262491	M	MP:0000599	enlarged liver	Gapvd1<em1(IMPC)Mbp>/Gapvd1<+>	C57BL/6N-Gapvd1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262491	F	MP:0000266	abnormal heart morphology	Gapvd1<em1(IMPC)Mbp>/Gapvd1<+>	C57BL/6N-Gapvd1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262491	F	MP:0001293	anophthalmia	Gapvd1<em1(IMPC)Mbp>/Gapvd1<+>	C57BL/6N-Gapvd1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262491	F	MP:0000691	enlarged spleen	Gapvd1<em1(IMPC)Mbp>/Gapvd1<+>	C57BL/6N-Gapvd1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262491	F	MP:0002135	abnormal kidney morphology	Gapvd1<em1(IMPC)Mbp>/Gapvd1<+>	C57BL/6N-Gapvd1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262491	F	MP:0003068	enlarged kidney	Gapvd1<em1(IMPC)Mbp>/Gapvd1<+>	C57BL/6N-Gapvd1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262491	F	MP:0002092	abnormal eye morphology	Gapvd1<em1(IMPC)Mbp>/Gapvd1<+>	C57BL/6N-Gapvd1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262491	M	MP:0000598	abnormal liver morphology	Gapvd1<em1(IMPC)Mbp>/Gapvd1<+>	C57BL/6N-Gapvd1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262494	F	MP:0002590	increased mean corpuscular volume	Gas7<em1(IMPC)J>/Gas7<em1(IMPC)J>	C57BL/6NJ-Gas7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262494	M	MP:0010024	increased total body fat amount	Gas7<em1(IMPC)J>/Gas7<em1(IMPC)J>	C57BL/6NJ-Gas7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262494	M	MP:0000063	decreased bone mineral density	Gas7<em1(IMPC)J>/Gas7<em1(IMPC)J>	C57BL/6NJ-Gas7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262494	M	MP:0010124	decreased bone mineral content	Gas7<em1(IMPC)J>/Gas7<em1(IMPC)J>	C57BL/6NJ-Gas7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262495	M	MP:0003984	embryonic growth retardation	Gata2<tm1b(KOMP)Wtsi>/Gata2<tm1b(KOMP)Wtsi>	C57BL/6N-Gata2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262495	M	MP:0001697	abnormal embryo size	Gata2<tm1b(KOMP)Wtsi>/Gata2<tm1b(KOMP)Wtsi>	C57BL/6N-Gata2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262496	M	MP:0001402	decreased locomotor activity	Gatad2b<tm1b(EUCOMM)Hmgu>/Gatad2b<+>	C57BL/6N-Gatad2b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262496	F	MP:0002968	increased circulating alkaline phosphatase level	Gatad2b<tm1b(EUCOMM)Hmgu>/Gatad2b<+>	C57BL/6N-Gatad2b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262496	M	MP:0000220	increased monocyte cell number	Gatad2b<tm1b(EUCOMM)Hmgu>/Gatad2b<+>	C57BL/6N-Gatad2b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262496	M	MP:0002590	increased mean corpuscular volume	Gatad2b<tm1b(EUCOMM)Hmgu>/Gatad2b<+>	C57BL/6N-Gatad2b<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262500	M	MP:0003928	increased heart rate variability	Gbp2<tm1b(KOMP)Wtsi>/Gbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Gbp2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262500	M	MP:0013279	increased fasting circulating glucose level	Gbp2<tm1b(KOMP)Wtsi>/Gbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Gbp2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262500	M	MP:0010506	prolonged RR interval	Gbp2<tm1b(KOMP)Wtsi>/Gbp2<tm1b(KOMP)Wtsi>	C57BL/6N-Gbp2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262502	F	MP:0005553	increased circulating creatinine level	Gbp5<em1(IMPC)Wtsi>/Gbp5<em1(IMPC)Wtsi>	C57BL/6N-Gbp5<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262504	M	MP:0002135	abnormal kidney morphology	Gcgr<tm1.1(KOMP)Vlcg>/Gcgr<tm1.1(KOMP)Vlcg>	C57BL/6N-Gcgr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262504	M	MP:0003917	increased kidney weight	Gcgr<tm1.1(KOMP)Vlcg>/Gcgr<tm1.1(KOMP)Vlcg>	C57BL/6N-Gcgr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262504	M	MP:0001925	male infertility	Gcgr<tm1.1(KOMP)Vlcg>/Gcgr<tm1.1(KOMP)Vlcg>	C57BL/6N-Gcgr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262504	F	MP:0001926	female infertility	Gcgr<tm1.1(KOMP)Vlcg>/Gcgr<tm1.1(KOMP)Vlcg>	C57BL/6N-Gcgr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262504	F	MP:0005565	increased blood urea nitrogen level	Gcgr<tm1.1(KOMP)Vlcg>/Gcgr<tm1.1(KOMP)Vlcg>	C57BL/6N-Gcgr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262504	F	MP:0000194	increased circulating calcium level	Gcgr<tm1.1(KOMP)Vlcg>/Gcgr<tm1.1(KOMP)Vlcg>	C57BL/6N-Gcgr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262504	M	MP:0003068	enlarged kidney	Gcgr<tm1.1(KOMP)Vlcg>/Gcgr<tm1.1(KOMP)Vlcg>	C57BL/6N-Gcgr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262504	M	MP:0002727	decreased circulating insulin level	Gcgr<tm1.1(KOMP)Vlcg>/Gcgr<tm1.1(KOMP)Vlcg>	C57BL/6N-Gcgr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262505	M	MP:0013279	increased fasting circulating glucose level	Gck<em1(IMPC)H>/Gck<+>	C57BL/6NTac-Gck<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262505	F	MP:0002968	increased circulating alkaline phosphatase level	Gck<em1(IMPC)H>/Gck<+>	C57BL/6NTac-Gck<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262507	M	MP:0003900	shortened QT interval	Gcsh<em1(IMPC)H>/Gcsh<+>	C57BL/6N-Gcsh<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262507	F	MP:0010506	prolonged RR interval	Gcsh<em1(IMPC)H>/Gcsh<+>	C57BL/6N-Gcsh<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262509	M	MP:0000703	abnormal thymus morphology	Gdap1<tm2b(KOMP)Wtsi>/Gdap1<tm2b(KOMP)Wtsi>	C57BL/6N-Gdap1<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262509	M	MP:0002631	abnormal epididymis morphology	Gdap1<tm2b(KOMP)Wtsi>/Gdap1<tm2b(KOMP)Wtsi>	C57BL/6N-Gdap1<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262509	M	MP:0002768	small adrenal glands	Gdap1<tm2b(KOMP)Wtsi>/Gdap1<tm2b(KOMP)Wtsi>	C57BL/6N-Gdap1<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262509	M	MP:0004931	enlarged epididymis	Gdap1<tm2b(KOMP)Wtsi>/Gdap1<tm2b(KOMP)Wtsi>	C57BL/6N-Gdap1<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262509	M	MP:0000706	small thymus	Gdap1<tm2b(KOMP)Wtsi>/Gdap1<tm2b(KOMP)Wtsi>	C57BL/6N-Gdap1<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262509	M	MP:0000639	abnormal adrenal gland morphology	Gdap1<tm2b(KOMP)Wtsi>/Gdap1<tm2b(KOMP)Wtsi>	C57BL/6N-Gdap1<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262509	F	MP:0001120	abnormal uterus morphology	Gdap1<tm2b(KOMP)Wtsi>/Gdap1<tm2b(KOMP)Wtsi>	C57BL/6N-Gdap1<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262509	M	MP:0002060	abnormal skin morphology	Gdap1<tm2b(KOMP)Wtsi>/Gdap1<tm2b(KOMP)Wtsi>	C57BL/6N-Gdap1<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262510	M	MP:0010025	decreased total body fat amount	Gdap2<em1(IMPC)Wtsi>/Gdap2<em1(IMPC)Wtsi>	C57BL/6N-Gdap2<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262510	M	MP:0005505	thrombocytosis	Gdap2<em1(IMPC)Wtsi>/Gdap2<em1(IMPC)Wtsi>	C57BL/6N-Gdap2<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262510	M	MP:0003960	increased lean body mass	Gdap2<em1(IMPC)Wtsi>/Gdap2<em1(IMPC)Wtsi>	C57BL/6N-Gdap2<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262510	M	MP:0008805	decreased circulating amylase level	Gdap2<em1(IMPC)Wtsi>/Gdap2<em1(IMPC)Wtsi>	C57BL/6N-Gdap2<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262510	M	MP:0005419	decreased circulating serum albumin level	Gdap2<em1(IMPC)Wtsi>/Gdap2<em1(IMPC)Wtsi>	C57BL/6N-Gdap2<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262510	M	MP:0000062	increased bone mineral density	Gdap2<em1(IMPC)Wtsi>/Gdap2<em1(IMPC)Wtsi>	C57BL/6N-Gdap2<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262510	M	MP:0010088	decreased circulating fructosamine level	Gdap2<em1(IMPC)Wtsi>/Gdap2<em1(IMPC)Wtsi>	C57BL/6N-Gdap2<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262510	M	MP:0005478	decreased circulating thyroxine level	Gdap2<em1(IMPC)Wtsi>/Gdap2<em1(IMPC)Wtsi>	C57BL/6N-Gdap2<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262511	M	MP:0010067	increased red blood cell distribution width	Gda<tm1a(KOMP)Wtsi>/Gda<tm1a(KOMP)Wtsi>	C57BL/6N-Gda<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262511	M	MP:0005419	decreased circulating serum albumin level	Gda<tm1a(KOMP)Wtsi>/Gda<tm1a(KOMP)Wtsi>	C57BL/6N-Gda<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262511	M	MP:0003960	increased lean body mass	Gda<tm1a(KOMP)Wtsi>/Gda<tm1a(KOMP)Wtsi>	C57BL/6N-Gda<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262511	M	MP:0000208	decreased hematocrit	Gda<tm1a(KOMP)Wtsi>/Gda<tm1a(KOMP)Wtsi>	C57BL/6N-Gda<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262511	M	MP:0010025	decreased total body fat amount	Gda<tm1a(KOMP)Wtsi>/Gda<tm1a(KOMP)Wtsi>	C57BL/6N-Gda<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262511	M	MP:0010123	increased bone mineral content	Gda<tm1a(KOMP)Wtsi>/Gda<tm1a(KOMP)Wtsi>	C57BL/6N-Gda<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262511	M	MP:0005179	decreased circulating cholesterol level	Gda<tm1a(KOMP)Wtsi>/Gda<tm1a(KOMP)Wtsi>	C57BL/6N-Gda<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262511	M	MP:0010088	decreased circulating fructosamine level	Gda<tm1a(KOMP)Wtsi>/Gda<tm1a(KOMP)Wtsi>	C57BL/6N-Gda<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262511	M	MP:0000062	increased bone mineral density	Gda<tm1a(KOMP)Wtsi>/Gda<tm1a(KOMP)Wtsi>	C57BL/6N-Gda<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262511	M	MP:0000186	decreased circulating HDL cholesterol level	Gda<tm1a(KOMP)Wtsi>/Gda<tm1a(KOMP)Wtsi>	C57BL/6N-Gda<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262512	F	MP:0002574	increased vertical activity	Gde1<tm1b(EUCOMM)Hmgu>/Gde1<+>	C57BL/6N-Gde1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262512	M	MP:0005178	increased circulating cholesterol level	Gde1<tm1b(EUCOMM)Hmgu>/Gde1<+>	C57BL/6N-Gde1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262512	M	MP:0010392	prolonged QRS complex duration	Gde1<tm1b(EUCOMM)Hmgu>/Gde1<+>	C57BL/6N-Gde1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262512	F	MP:0002968	increased circulating alkaline phosphatase level	Gde1<tm1b(EUCOMM)Hmgu>/Gde1<+>	C57BL/6N-Gde1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262513	F	MP:0002757	decreased vertical activity	Gde1<tm1b(EUCOMM)Hmgu>/Gde1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gde1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262513	F	MP:0001406	abnormal gait	Gde1<tm1b(EUCOMM)Hmgu>/Gde1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gde1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262513	F	MP:0001489	decreased startle reflex	Gde1<tm1b(EUCOMM)Hmgu>/Gde1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gde1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262514	F	MP:0003743	abnormal facial morphology	Gdf11<tm2b(EUCOMM)Hmgu>/Gdf11<tm2b(EUCOMM)Hmgu>	C57BL/6N-Gdf11<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262514	F	MP:0000428	abnormal craniofacial morphology	Gdf11<tm2b(EUCOMM)Hmgu>/Gdf11<tm2b(EUCOMM)Hmgu>	C57BL/6N-Gdf11<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262515	M	MP:0013279	increased fasting circulating glucose level	Gdpd2<tm1a(KOMP)Wtsi>/Y	C57BL/6N-Gdpd2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262517	M	MP:0002965	increased circulating serum albumin level	Gfi1b<tm1b(EUCOMM)Hmgu>/Gfi1b<+>	C57BL/6N-Gfi1b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262517	M	MP:0010024	increased total body fat amount	Gfi1b<tm1b(EUCOMM)Hmgu>/Gfi1b<+>	C57BL/6N-Gfi1b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262517	M	MP:0000222	decreased neutrophil cell number	Gfi1b<tm1b(EUCOMM)Hmgu>/Gfi1b<+>	C57BL/6N-Gfi1b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262517	M	MP:0005013	increased lymphocyte cell number	Gfi1b<tm1b(EUCOMM)Hmgu>/Gfi1b<+>	C57BL/6N-Gfi1b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262520	F	MP:0003795	abnormal bone structure	Ghrh<tm1b(EUCOMM)Wtsi>/Ghrh<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ghrh<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262520	M	MP:0010053	decreased grip strength	Ghrh<tm1b(EUCOMM)Wtsi>/Ghrh<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ghrh<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262521	M	MP:0002875	decreased erythrocyte cell number	Gigyf2<tm1b(EUCOMM)Wtsi>/Gigyf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gigyf2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262521	M	MP:0001147	small testis	Gigyf2<tm1b(EUCOMM)Wtsi>/Gigyf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gigyf2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262521	F	MP:0000745	tremors	Gigyf2<tm1b(EUCOMM)Wtsi>/Gigyf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gigyf2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262521	M	MP:0000208	decreased hematocrit	Gigyf2<tm1b(EUCOMM)Wtsi>/Gigyf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gigyf2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262521	F	MP:0001566	increased circulating phosphate level	Gigyf2<tm1b(EUCOMM)Wtsi>/Gigyf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gigyf2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262521	M	MP:0002874	decreased hemoglobin content	Gigyf2<tm1b(EUCOMM)Wtsi>/Gigyf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gigyf2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262521	F	MP:0013279	increased fasting circulating glucose level	Gigyf2<tm1b(EUCOMM)Wtsi>/Gigyf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gigyf2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262521	M	MP:0005012	decreased eosinophil cell number	Gigyf2<tm1b(EUCOMM)Wtsi>/Gigyf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gigyf2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262521	F	MP:0010067	increased red blood cell distribution width	Gigyf2<tm1b(EUCOMM)Wtsi>/Gigyf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gigyf2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262521	F	MP:0004952	increased spleen weight	Gigyf2<tm1b(EUCOMM)Wtsi>/Gigyf2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Gigyf2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262523	M	MP:0006415	absent testes	Gja10<em2(IMPC)Mbp>/Gja10<em2(IMPC)Mbp>	C57BL/6N-Gja10<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262523	M	MP:0002059	abnormal seminal vesicle morphology	Gja10<em2(IMPC)Mbp>/Gja10<em2(IMPC)Mbp>	C57BL/6N-Gja10<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262523	M	MP:0004727	absent epididymis	Gja10<em2(IMPC)Mbp>/Gja10<em2(IMPC)Mbp>	C57BL/6N-Gja10<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262523	M	MP:0001157	small seminal vesicle	Gja10<em2(IMPC)Mbp>/Gja10<em2(IMPC)Mbp>	C57BL/6N-Gja10<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262523	M	MP:0002631	abnormal epididymis morphology	Gja10<em2(IMPC)Mbp>/Gja10<em2(IMPC)Mbp>	C57BL/6N-Gja10<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262523	M	MP:0001146	abnormal testis morphology	Gja10<em2(IMPC)Mbp>/Gja10<em2(IMPC)Mbp>	C57BL/6N-Gja10<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262525	M	MP:0010053	decreased grip strength	Gjd4<tm1.1(KOMP)Vlcg>/Gjd4<tm1.1(KOMP)Vlcg>	C57BL/6N-Gjd4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262526	M	MP:0010068	decreased red blood cell distribution width	Glra2<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Glra2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262526	M	MP:0005013	increased lymphocyte cell number	Glra2<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Glra2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262526	M	MP:0010087	increased circulating fructosamine level	Glra2<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Glra2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262526	M	MP:0002591	decreased mean corpuscular volume	Glra2<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Glra2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262526	M	MP:0000222	decreased neutrophil cell number	Glra2<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Glra2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262526	M	MP:0000223	decreased monocyte cell number	Glra2<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Glra2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262526	M	MP:0008806	increased circulating amylase level	Glra2<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Glra2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262527	M	MP:0000182	increased circulating LDL cholesterol level	Glra4<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Glra4<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262528	M	MP:0002966	decreased circulating alkaline phosphatase level	Glrb<em1(IMPC)Tcp>/Glrb<+>	C57BL/6NCrl-Glrb<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262528	M	MP:0002833	increased heart weight	Glrb<em1(IMPC)Tcp>/Glrb<+>	C57BL/6NCrl-Glrb<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262528	M	MP:0020422	decreased freezing behavior	Glrb<em1(IMPC)Tcp>/Glrb<+>	C57BL/6NCrl-Glrb<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262528	M	MP:0005419	decreased circulating serum albumin level	Glrb<em1(IMPC)Tcp>/Glrb<+>	C57BL/6NCrl-Glrb<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262528	M	MP:0004952	increased spleen weight	Glrb<em1(IMPC)Tcp>/Glrb<+>	C57BL/6NCrl-Glrb<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262528	M	MP:0002941	increased circulating alanine transaminase level	Glrb<em1(IMPC)Tcp>/Glrb<+>	C57BL/6NCrl-Glrb<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262528	M	MP:0000219	increased neutrophil cell number	Glrb<em1(IMPC)Tcp>/Glrb<+>	C57BL/6NCrl-Glrb<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262528	M	MP:0005343	increased circulating aspartate transaminase level	Glrb<em1(IMPC)Tcp>/Glrb<+>	C57BL/6NCrl-Glrb<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262531	F	MP:0001312	abnormal cornea morphology	Glyctk<em1(IMPC)J>/Glyctk<em1(IMPC)J>	C57BL/6NJ-Glyctk<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262532	F	MP:0009709	hydrometra	Gm14496<em2(IMPC)Mbp>/Gm14496<em2(IMPC)Mbp>	C57BL/6N-Gm14496<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262532	F	MP:0001120	abnormal uterus morphology	Gm14496<em2(IMPC)Mbp>/Gm14496<em2(IMPC)Mbp>	C57BL/6N-Gm14496<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262532	M	MP:0000494	abnormal cecum morphology	Gm14496<em2(IMPC)Mbp>/Gm14496<em2(IMPC)Mbp>	C57BL/6N-Gm14496<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262532	M	MP:0002631	abnormal epididymis morphology	Gm14496<em2(IMPC)Mbp>/Gm14496<em2(IMPC)Mbp>	C57BL/6N-Gm14496<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262532	M	MP:0004931	enlarged epididymis	Gm14496<em2(IMPC)Mbp>/Gm14496<em2(IMPC)Mbp>	C57BL/6N-Gm14496<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262533	M	MP:0000182	increased circulating LDL cholesterol level	Gm20646<em1(IMPC)Wtsi>/Gm20646<em1(IMPC)Wtsi>	C57BL/6N-Gm20646<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262534	M	MP:0000702	enlarged lymph nodes	Gm4922<em1(IMPC)Tcp>/Gm4922<em1(IMPC)Tcp>	C57BL/6NCrl-Gm4922<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262534	M	MP:0002590	increased mean corpuscular volume	Gm4922<em1(IMPC)Tcp>/Gm4922<em1(IMPC)Tcp>	C57BL/6NCrl-Gm4922<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262534	M	MP:0009142	decreased prepulse inhibition	Gm4922<em1(IMPC)Tcp>/Gm4922<em1(IMPC)Tcp>	C57BL/6NCrl-Gm4922<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262534	F	MP:0000062	increased bone mineral density	Gm4922<em1(IMPC)Tcp>/Gm4922<em1(IMPC)Tcp>	C57BL/6NCrl-Gm4922<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262536	F	MP:0005560	decreased circulating glucose level	Gm572<tm1b(EUCOMM)Hmgu>/Gm572<+>	C57BL/6N-Gm572<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262536	M	MP:0006243	impaired pupillary reflex	Gm572<tm1b(EUCOMM)Hmgu>/Gm572<+>	C57BL/6N-Gm572<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262538	M	MP:0001258	decreased body length	Gm6578<tm1a(KOMP)Wtsi>/Gm6578<tm1a(KOMP)Wtsi>	C57BL/6N-Gm6578<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262539	M	MP:0000274	enlarged heart	Ctag2l2<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Ctag2l2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262540	M	MP:0010024	increased total body fat amount	Gm94<tm1b(KOMP)Wtsi>/Gm94<+>	C57BL/6N-Gm94<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262540	F	MP:0002574	increased vertical activity	Gm94<tm1b(KOMP)Wtsi>/Gm94<+>	C57BL/6N-Gm94<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262540	M	MP:0003961	decreased lean body mass	Gm94<tm1b(KOMP)Wtsi>/Gm94<+>	C57BL/6N-Gm94<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262540	M	MP:0005178	increased circulating cholesterol level	Gm94<tm1b(KOMP)Wtsi>/Gm94<+>	C57BL/6N-Gm94<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262542	M	MP:0001718	abnormal visceral yolk sac morphology	Gna13<tm1b(KOMP)Wtsi>/Gna13<tm1b(KOMP)Wtsi>	C57BL/6N-Gna13<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262543	F	MP:0002626	increased heart rate	Gnb2<em1(IMPC)J>/Gnb2<em1(IMPC)J>	C57BL/6NJ-Gnb2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262543	F	MP:0005561	increased mean corpuscular hemoglobin	Gnb2<em1(IMPC)J>/Gnb2<em1(IMPC)J>	C57BL/6NJ-Gnb2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262543	F	MP:0010507	shortened RR interval	Gnb2<em1(IMPC)J>/Gnb2<em1(IMPC)J>	C57BL/6NJ-Gnb2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262543	F	MP:0005567	decreased circulating total protein level	Gnb2<em1(IMPC)J>/Gnb2<em1(IMPC)J>	C57BL/6NJ-Gnb2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262543	F	MP:0010053	decreased grip strength	Gnb2<em1(IMPC)J>/Gnb2<em1(IMPC)J>	C57BL/6NJ-Gnb2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262543	F	MP:0005419	decreased circulating serum albumin level	Gnb2<em1(IMPC)J>/Gnb2<em1(IMPC)J>	C57BL/6NJ-Gnb2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262543	F	MP:0002574	increased vertical activity	Gnb2<em1(IMPC)J>/Gnb2<em1(IMPC)J>	C57BL/6NJ-Gnb2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262543	F	MP:0005278	abnormal cholesterol homeostasis	Gnb2<em1(IMPC)J>/Gnb2<em1(IMPC)J>	C57BL/6NJ-Gnb2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262544	M	MP:0000691	enlarged spleen	Gnb4<em1(IMPC)H>/Gnb4<em1(IMPC)H>	C57BL/6NTac-Gnb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262544	F	MP:0002968	increased circulating alkaline phosphatase level	Gnb4<em1(IMPC)H>/Gnb4<em1(IMPC)H>	C57BL/6NTac-Gnb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262544	F	MP:0001364	decreased anxiety-related response	Gnb4<em1(IMPC)H>/Gnb4<em1(IMPC)H>	C57BL/6NTac-Gnb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262544	F	MP:0001399	hyperactivity	Gnb4<em1(IMPC)H>/Gnb4<em1(IMPC)H>	C57BL/6NTac-Gnb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262544	M	MP:0010052	increased grip strength	Gnb4<em1(IMPC)H>/Gnb4<em1(IMPC)H>	C57BL/6NTac-Gnb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262544	M	MP:0000274	enlarged heart	Gnb4<em1(IMPC)H>/Gnb4<em1(IMPC)H>	C57BL/6NTac-Gnb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262545	F	MP:0005344	increased circulating bilirubin level	Golga5<tm1b(KOMP)Wtsi>/Golga5<tm1b(KOMP)Wtsi>	C57BL/6N-Golga5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262545	M	MP:0000208	decreased hematocrit	Golga5<tm1b(KOMP)Wtsi>/Golga5<tm1b(KOMP)Wtsi>	C57BL/6N-Golga5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262545	M	MP:0002874	decreased hemoglobin content	Golga5<tm1b(KOMP)Wtsi>/Golga5<tm1b(KOMP)Wtsi>	C57BL/6N-Golga5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262545	M	MP:0001488	increased startle reflex	Golga5<tm1b(KOMP)Wtsi>/Golga5<tm1b(KOMP)Wtsi>	C57BL/6N-Golga5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262545	M	MP:0002875	decreased erythrocyte cell number	Golga5<tm1b(KOMP)Wtsi>/Golga5<tm1b(KOMP)Wtsi>	C57BL/6N-Golga5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262548	M	MP:0010506	prolonged RR interval	Got1<tm1b(EUCOMM)Hmgu>/Got1<+>	C57BL/6N-Got1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262548	F	MP:0005560	decreased circulating glucose level	Got1<tm1b(EUCOMM)Hmgu>/Got1<+>	C57BL/6N-Got1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262548	M	MP:0005016	decreased lymphocyte cell number	Got1<tm1b(EUCOMM)Hmgu>/Got1<+>	C57BL/6N-Got1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262548	M	MP:0000221	decreased leukocyte cell number	Got1<tm1b(EUCOMM)Hmgu>/Got1<+>	C57BL/6N-Got1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262548	M	MP:0002607	decreased basophil cell number	Got1<tm1b(EUCOMM)Hmgu>/Got1<+>	C57BL/6N-Got1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262550	M	MP:0001146	abnormal testis morphology	Gp1bb<tm1.1(KOMP)Vlcg>/Gp1bb<tm1.1(KOMP)Vlcg>	C57BL/6N-Gp1bb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262550	M	MP:0001147	small testis	Gp1bb<tm1.1(KOMP)Vlcg>/Gp1bb<tm1.1(KOMP)Vlcg>	C57BL/6N-Gp1bb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262550	F	MP:0001120	abnormal uterus morphology	Gp1bb<tm1.1(KOMP)Vlcg>/Gp1bb<tm1.1(KOMP)Vlcg>	C57BL/6N-Gp1bb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262550	F	MP:0009709	hydrometra	Gp1bb<tm1.1(KOMP)Vlcg>/Gp1bb<tm1.1(KOMP)Vlcg>	C57BL/6N-Gp1bb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262551	F	MP:0008528	polycystic kidney	Gpa33<tm2b(KOMP)Wtsi>/Gpa33<tm2b(KOMP)Wtsi>	C57BL/6N-Gpa33<tm2b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262551	M	MP:0010052	increased grip strength	Gpa33<tm2b(KOMP)Wtsi>/Gpa33<tm2b(KOMP)Wtsi>	C57BL/6N-Gpa33<tm2b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262551	F	MP:0001293	anophthalmia	Gpa33<tm2b(KOMP)Wtsi>/Gpa33<tm2b(KOMP)Wtsi>	C57BL/6N-Gpa33<tm2b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262551	F	MP:0001120	abnormal uterus morphology	Gpa33<tm2b(KOMP)Wtsi>/Gpa33<tm2b(KOMP)Wtsi>	C57BL/6N-Gpa33<tm2b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262554	M	MP:0001406	abnormal gait	Gpbp1<tm1b(EUCOMM)Wtsi>/Gpbp1<+>	C57BL/6N-Gpbp1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262554	F	MP:0005344	increased circulating bilirubin level	Gpbp1<tm1b(EUCOMM)Wtsi>/Gpbp1<+>	C57BL/6N-Gpbp1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262554	M	MP:0002059	abnormal seminal vesicle morphology	Gpbp1<tm1b(EUCOMM)Wtsi>/Gpbp1<+>	C57BL/6N-Gpbp1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262554	M	MP:0010511	shortened PR interval	Gpbp1<tm1b(EUCOMM)Wtsi>/Gpbp1<+>	C57BL/6N-Gpbp1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262554	M	MP:0011954	shortened PQ interval	Gpbp1<tm1b(EUCOMM)Wtsi>/Gpbp1<+>	C57BL/6N-Gpbp1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262556	M	MP:0020870	decreased thigmotaxis	Gpr101<tm1b(KOMP)Mbp>/Y	C57BL/6N-Gpr101<tm1b(KOMP)Mbp>/Ics	N	MGI:5576271
MGI:6262556	M	MP:0004924	abnormal behavior	Gpr101<tm1b(KOMP)Mbp>/Y	C57BL/6N-Gpr101<tm1b(KOMP)Mbp>/Ics	N	MGI:5576271
MGI:6262556	M	MP:0001364	decreased anxiety-related response	Gpr101<tm1b(KOMP)Mbp>/Y	C57BL/6N-Gpr101<tm1b(KOMP)Mbp>/Ics	N	MGI:5576271
MGI:6262556	M	MP:0001402	decreased locomotor activity	Gpr101<tm1b(KOMP)Mbp>/Y	C57BL/6N-Gpr101<tm1b(KOMP)Mbp>/Ics	N	MGI:5576271
MGI:6262559	F	MP:0000266	abnormal heart morphology	Gpr139<tm1.1(KOMP)Vlcg>/Gpr139<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpr139<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262559	F	MP:0000274	enlarged heart	Gpr139<tm1.1(KOMP)Vlcg>/Gpr139<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpr139<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262559	F	MP:0011110	preweaning lethality, incomplete penetrance	Gpr139<tm1.1(KOMP)Vlcg>/Gpr139<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpr139<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262561	F	MP:0001399	hyperactivity	Gpr153<em1(IMPC)J>/Gpr153<em1(IMPC)J>	C57BL/6NJ-Gpr153<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262561	M	MP:0010053	decreased grip strength	Gpr153<em1(IMPC)J>/Gpr153<em1(IMPC)J>	C57BL/6NJ-Gpr153<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262562	F	MP:0002339	abnormal lymph node morphology	Gpr155<em1(IMPC)Mbp>/Gpr155<em1(IMPC)Mbp>	C57BL/6N-Gpr155<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262562	F	MP:0000702	enlarged lymph nodes	Gpr155<em1(IMPC)Mbp>/Gpr155<em1(IMPC)Mbp>	C57BL/6N-Gpr155<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262562	M	MP:0001157	small seminal vesicle	Gpr155<em1(IMPC)Mbp>/Gpr155<em1(IMPC)Mbp>	C57BL/6N-Gpr155<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262562	M	MP:0003068	enlarged kidney	Gpr155<em1(IMPC)Mbp>/Gpr155<em1(IMPC)Mbp>	C57BL/6N-Gpr155<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262562	M	MP:0002059	abnormal seminal vesicle morphology	Gpr155<em1(IMPC)Mbp>/Gpr155<em1(IMPC)Mbp>	C57BL/6N-Gpr155<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262562	M	MP:0002135	abnormal kidney morphology	Gpr155<em1(IMPC)Mbp>/Gpr155<em1(IMPC)Mbp>	C57BL/6N-Gpr155<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262563	M	MP:0010124	decreased bone mineral content	Gpr15<em1(IMPC)J>/Gpr15<em1(IMPC)J>	C57BL/6NJ-Gpr15<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262563	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Gpr15<em1(IMPC)J>/Gpr15<em1(IMPC)J>	C57BL/6NJ-Gpr15<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262563	M	MP:0005293	impaired glucose tolerance	Gpr15<em1(IMPC)J>/Gpr15<em1(IMPC)J>	C57BL/6NJ-Gpr15<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262563	M	MP:0010024	increased total body fat amount	Gpr15<em1(IMPC)J>/Gpr15<em1(IMPC)J>	C57BL/6NJ-Gpr15<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262563	M	MP:0005562	decreased mean corpuscular hemoglobin	Gpr15<em1(IMPC)J>/Gpr15<em1(IMPC)J>	C57BL/6NJ-Gpr15<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262563	M	MP:0003961	decreased lean body mass	Gpr15<em1(IMPC)J>/Gpr15<em1(IMPC)J>	C57BL/6NJ-Gpr15<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262564	F	MP:0002599	increased mean platelet volume	Gpr17<tm1b(KOMP)Mbp>/Gpr17<tm1b(KOMP)Mbp>	C57BL/6N-Gpr17<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6262564	F	MP:0000219	increased neutrophil cell number	Gpr17<tm1b(KOMP)Mbp>/Gpr17<tm1b(KOMP)Mbp>	C57BL/6N-Gpr17<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6262566	F	MP:0001284	absent vibrissae	Gpr34<tm1.1(KOMP)Vlcg>/Gpr34<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpr34<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262567	F	MP:0002135	abnormal kidney morphology	Gpr39<em1(IMPC)Mbp>/Gpr39<em1(IMPC)Mbp>	C57BL/6N-Gpr39<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262567	F	MP:0008528	polycystic kidney	Gpr39<em1(IMPC)Mbp>/Gpr39<em1(IMPC)Mbp>	C57BL/6N-Gpr39<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262568	F	MP:0000274	enlarged heart	Gprc6a<tm1.1(KOMP)Vlcg>/Gprc6a<+>	C57BL/6N-Gprc6a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262568	F	MP:0000266	abnormal heart morphology	Gprc6a<tm1.1(KOMP)Vlcg>/Gprc6a<+>	C57BL/6N-Gprc6a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262569	M	MP:0004955	increased thymus weight	Gprc6a<tm1.1(KOMP)Vlcg>/Gprc6a<tm1.1(KOMP)Vlcg>	C57BL/6N-Gprc6a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262569	F	MP:0005564	increased hemoglobin content	Gprc6a<tm1.1(KOMP)Vlcg>/Gprc6a<tm1.1(KOMP)Vlcg>	C57BL/6N-Gprc6a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262570	F	MP:0000274	enlarged heart	Gpx5<tm1.1(KOMP)Vlcg>/Gpx5<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpx5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262570	F	MP:0000266	abnormal heart morphology	Gpx5<tm1.1(KOMP)Vlcg>/Gpx5<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpx5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262571	F	MP:0001399	hyperactivity	Gpx6<em1(IMPC)J>/Gpx6<em1(IMPC)J>	C57BL/6NJ-Gpx6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262572	F	MP:0003131	increased erythrocyte cell number	Gpx7<tm1.1(KOMP)Vlcg>/Gpx7<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpx7<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262572	F	MP:0011110	preweaning lethality, incomplete penetrance	Gpx7<tm1.1(KOMP)Vlcg>/Gpx7<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpx7<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262572	F	MP:0001333	absent optic nerve	Gpx7<tm1.1(KOMP)Vlcg>/Gpx7<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpx7<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262572	F	MP:0002092	abnormal eye morphology	Gpx7<tm1.1(KOMP)Vlcg>/Gpx7<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpx7<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262572	F	MP:0002608	increased hematocrit	Gpx7<tm1.1(KOMP)Vlcg>/Gpx7<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpx7<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262573	M	MP:0001491	unresponsive to tactile stimuli	Gramd1b<em1(IMPC)J>/Gramd1b<em1(IMPC)J>	C57BL/6NJ-Gramd1b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262573	M	MP:0002111	abnormal tail morphology	Gramd1b<em1(IMPC)J>/Gramd1b<em1(IMPC)J>	C57BL/6NJ-Gramd1b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262574	M	MP:0013278	decreased fasting circulating glucose level	Gramd1c<tm1b(KOMP)Wtsi>/Gramd1c<tm1b(KOMP)Wtsi>	C57BL/6N-Gramd1c<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262574	M	MP:0001513	limb grasping	Gramd1c<tm1b(KOMP)Wtsi>/Gramd1c<tm1b(KOMP)Wtsi>	C57BL/6N-Gramd1c<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262574	F	MP:0005343	increased circulating aspartate transaminase level	Gramd1c<tm1b(KOMP)Wtsi>/Gramd1c<tm1b(KOMP)Wtsi>	C57BL/6N-Gramd1c<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262574	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Gramd1c<tm1b(KOMP)Wtsi>/Gramd1c<tm1b(KOMP)Wtsi>	C57BL/6N-Gramd1c<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262574	M	MP:0001552	increased circulating triglyceride level	Gramd1c<tm1b(KOMP)Wtsi>/Gramd1c<tm1b(KOMP)Wtsi>	C57BL/6N-Gramd1c<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262574	M	MP:0005561	increased mean corpuscular hemoglobin	Gramd1c<tm1b(KOMP)Wtsi>/Gramd1c<tm1b(KOMP)Wtsi>	C57BL/6N-Gramd1c<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262574	F	MP:0002959	increased urine microalbumin level	Gramd1c<tm1b(KOMP)Wtsi>/Gramd1c<tm1b(KOMP)Wtsi>	C57BL/6N-Gramd1c<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262576	M	MP:0010024	increased total body fat amount	Greb1l<em1(IMPC)J>/Greb1l<+>	C57BL/6NJ-Greb1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262576	F	MP:0001304	cataract	Greb1l<em1(IMPC)J>/Greb1l<+>	C57BL/6NJ-Greb1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262576	M	MP:0003961	decreased lean body mass	Greb1l<em1(IMPC)J>/Greb1l<+>	C57BL/6NJ-Greb1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262579	M	MP:0005344	increased circulating bilirubin level	Grin3b<tm1b(KOMP)Wtsi>/Grin3b<tm1b(KOMP)Wtsi>	C57BL/6N-Grin3b<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262579	F	MP:0005627	increased circulating potassium level	Grin3b<tm1b(KOMP)Wtsi>/Grin3b<tm1b(KOMP)Wtsi>	C57BL/6N-Grin3b<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262579	M	MP:0010067	increased red blood cell distribution width	Grin3b<tm1b(KOMP)Wtsi>/Grin3b<tm1b(KOMP)Wtsi>	C57BL/6N-Grin3b<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262579	F	MP:0001406	abnormal gait	Grin3b<tm1b(KOMP)Wtsi>/Grin3b<tm1b(KOMP)Wtsi>	C57BL/6N-Grin3b<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262579	M	MP:0002644	decreased circulating triglyceride level	Grin3b<tm1b(KOMP)Wtsi>/Grin3b<tm1b(KOMP)Wtsi>	C57BL/6N-Grin3b<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262580	M	MP:0000274	enlarged heart	Grk5<tm1b(KOMP)Mbp>/Grk5<tm1b(KOMP)Mbp>	C57BL/6N-Grk5<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262580	M	MP:0000266	abnormal heart morphology	Grk5<tm1b(KOMP)Mbp>/Grk5<tm1b(KOMP)Mbp>	C57BL/6N-Grk5<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262580	M	MP:0002135	abnormal kidney morphology	Grk5<tm1b(KOMP)Mbp>/Grk5<tm1b(KOMP)Mbp>	C57BL/6N-Grk5<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262582	F	MP:0001523	impaired righting response	Grm7<em1(IMPC)H>/Grm7<em1(IMPC)H>	C57BL/6NTac-Grm7<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262582	F	MP:0002599	increased mean platelet volume	Grm7<em1(IMPC)H>/Grm7<em1(IMPC)H>	C57BL/6NTac-Grm7<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262582	M	MP:0010052	increased grip strength	Grm7<em1(IMPC)H>/Grm7<em1(IMPC)H>	C57BL/6NTac-Grm7<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262584	M	MP:0005561	increased mean corpuscular hemoglobin	Gsdma3<tm1(KOMP)Vlcg>/Gsdma3<tm1(KOMP)Vlcg>	C57BL/6N-Gsdma3<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:6262584	M	MP:0002875	decreased erythrocyte cell number	Gsdma3<tm1(KOMP)Vlcg>/Gsdma3<tm1(KOMP)Vlcg>	C57BL/6N-Gsdma3<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:6262584	M	MP:0000208	decreased hematocrit	Gsdma3<tm1(KOMP)Vlcg>/Gsdma3<tm1(KOMP)Vlcg>	C57BL/6N-Gsdma3<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:6262584	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Gsdma3<tm1(KOMP)Vlcg>/Gsdma3<tm1(KOMP)Vlcg>	C57BL/6N-Gsdma3<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:6262584	F	MP:0005013	increased lymphocyte cell number	Gsdma3<tm1(KOMP)Vlcg>/Gsdma3<tm1(KOMP)Vlcg>	C57BL/6N-Gsdma3<tm1(KOMP)Vlcg>/Nju	N	MGI:5576271
MGI:6262586	F	MP:0008935	decreased mean platelet volume	Gsk3a<tm1b(EUCOMM)Hmgu>/Gsk3a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gsk3a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262586	M	MP:0001417	decreased exploration in new environment	Gsk3a<tm1b(EUCOMM)Hmgu>/Gsk3a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gsk3a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262586	F	MP:0010392	prolonged QRS complex duration	Gsk3a<tm1b(EUCOMM)Hmgu>/Gsk3a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gsk3a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262586	M	MP:0003960	increased lean body mass	Gsk3a<tm1b(EUCOMM)Hmgu>/Gsk3a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gsk3a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262586	M	MP:0005292	improved glucose tolerance	Gsk3a<tm1b(EUCOMM)Hmgu>/Gsk3a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gsk3a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262587	F	MP:0003795	abnormal bone structure	Gspt2<tm1.1(KOMP)Vlcg>/Gspt2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gspt2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262588	F	MP:0005560	decreased circulating glucose level	Gstm6<tm1b(EUCOMM)Hmgu>/Gstm6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gstm6<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262589	F	MP:0001510	abnormal coat appearance	Gsto1<em1(IMPC)J>/Gsto1<em1(IMPC)J>	C57BL/6NJ-Gsto1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262589	F	MP:0010124	decreased bone mineral content	Gsto1<em1(IMPC)J>/Gsto1<em1(IMPC)J>	C57BL/6NJ-Gsto1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262589	M	MP:0001488	increased startle reflex	Gsto1<em1(IMPC)J>/Gsto1<em1(IMPC)J>	C57BL/6NJ-Gsto1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262589	F	MP:0005562	decreased mean corpuscular hemoglobin	Gsto1<em1(IMPC)J>/Gsto1<em1(IMPC)J>	C57BL/6NJ-Gsto1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262595	F	MP:0005567	decreased circulating total protein level	H2ab3<em1(IMPC)Wtsi>/H2ab3<em1(IMPC)Wtsi>	C57BL/6N-H2ab3<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:6262595	F	MP:0005419	decreased circulating serum albumin level	H2ab3<em1(IMPC)Wtsi>/H2ab3<em1(IMPC)Wtsi>	C57BL/6N-H2ab3<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:6262596	M	MP:0001925	male infertility	H2al2a<em1(IMPC)Wtsi>/H2al2a<em1(IMPC)Wtsi>	C57BL/6N-H2al2a<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262597	F	MP:0005344	increased circulating bilirubin level	H2-T24<em1(IMPC)Wtsi>/H2-T24<em1(IMPC)Wtsi>	C57BL/6N-H2-T24<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262597	F	MP:0005567	decreased circulating total protein level	H2-T24<em1(IMPC)Wtsi>/H2-T24<em1(IMPC)Wtsi>	C57BL/6N-H2-T24<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262597	F	MP:0000218	increased leukocyte cell number	H2-T24<em1(IMPC)Wtsi>/H2-T24<em1(IMPC)Wtsi>	C57BL/6N-H2-T24<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262598	M	MP:0008528	polycystic kidney	H3f3b<tm1.1(KOMP)Mbp>/H3f3b<tm1.1(KOMP)Mbp>	C57BL/6N-H3f3b<tm1.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6262598	F	MP:0001488	increased startle reflex	H3f3b<tm1.1(KOMP)Mbp>/H3f3b<tm1.1(KOMP)Mbp>	C57BL/6N-H3f3b<tm1.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6262598	M	MP:0002135	abnormal kidney morphology	H3f3b<tm1.1(KOMP)Mbp>/H3f3b<tm1.1(KOMP)Mbp>	C57BL/6N-H3f3b<tm1.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6262603	M	MP:0005562	decreased mean corpuscular hemoglobin	Hbq1a<tm1.1(KOMP)Vlcg>/Hbq1a<tm1.1(KOMP)Vlcg>	C57BL/6N-Hbq1a<tm1.1(KOMP)Vlcg>/Rbrc	N	MGI:5576271
MGI:6262605	M	MP:0001417	decreased exploration in new environment	Hdac1<tm1b(EUCOMM)Wtsi>/Hdac1<+>	C57BL/6N-Hdac1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262605	F	MP:0005562	decreased mean corpuscular hemoglobin	Hdac1<tm1b(EUCOMM)Wtsi>/Hdac1<+>	C57BL/6N-Hdac1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262608	F	MP:0005419	decreased circulating serum albumin level	Hdgfl1<em1(IMPC)Tcp>/Hdgfl1<+>	C57BL/6NCrl-Hdgfl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262608	M	MP:0001147	small testis	Hdgfl1<em1(IMPC)Tcp>/Hdgfl1<+>	C57BL/6NCrl-Hdgfl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262608	M	MP:0002833	increased heart weight	Hdgfl1<em1(IMPC)Tcp>/Hdgfl1<+>	C57BL/6NCrl-Hdgfl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262610	M	MP:0002092	abnormal eye morphology	Hdgfl3<em1(IMPC)Tcp>/Hdgfl3<em1(IMPC)Tcp>	C57BL/6NCrl-Hdgfl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262610	F	MP:0010124	decreased bone mineral content	Hdgfl3<em1(IMPC)Tcp>/Hdgfl3<em1(IMPC)Tcp>	C57BL/6NCrl-Hdgfl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262610	M	MP:0002060	abnormal skin morphology	Hdgfl3<em1(IMPC)Tcp>/Hdgfl3<em1(IMPC)Tcp>	C57BL/6NCrl-Hdgfl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262610	F	MP:0001258	decreased body length	Hdgfl3<em1(IMPC)Tcp>/Hdgfl3<em1(IMPC)Tcp>	C57BL/6NCrl-Hdgfl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262611	M	MP:0002606	increased basophil cell number	Hectd1<tm1b(EUCOMM)Hmgu>/Hectd1<+>	C57BL/6N-Hectd1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:6262611	F	MP:0002966	decreased circulating alkaline phosphatase level	Hectd1<tm1b(EUCOMM)Hmgu>/Hectd1<+>	C57BL/6N-Hectd1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:6262611	F	MP:0000194	increased circulating calcium level	Hectd1<tm1b(EUCOMM)Hmgu>/Hectd1<+>	C57BL/6N-Hectd1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:6262611	M	MP:0005011	increased eosinophil cell number	Hectd1<tm1b(EUCOMM)Hmgu>/Hectd1<+>	C57BL/6N-Hectd1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:6262611	F	MP:0002075	abnormal coat/hair pigmentation	Hectd1<tm1b(EUCOMM)Hmgu>/Hectd1<+>	C57BL/6N-Hectd1<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:6262612	M	MP:0001566	increased circulating phosphate level	Hecw1<tm2b(EUCOMM)Hmgu>/Hecw1<tm2b(EUCOMM)Hmgu>	C57BL/6N-Hecw1<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262612	F	MP:0001523	impaired righting response	Hecw1<tm2b(EUCOMM)Hmgu>/Hecw1<tm2b(EUCOMM)Hmgu>	C57BL/6N-Hecw1<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262612	M	MP:0000745	tremors	Hecw1<tm2b(EUCOMM)Hmgu>/Hecw1<tm2b(EUCOMM)Hmgu>	C57BL/6N-Hecw1<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262612	M	MP:0001513	limb grasping	Hecw1<tm2b(EUCOMM)Hmgu>/Hecw1<tm2b(EUCOMM)Hmgu>	C57BL/6N-Hecw1<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262612	M	MP:0013278	decreased fasting circulating glucose level	Hecw1<tm2b(EUCOMM)Hmgu>/Hecw1<tm2b(EUCOMM)Hmgu>	C57BL/6N-Hecw1<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262612	M	MP:0001417	decreased exploration in new environment	Hecw1<tm2b(EUCOMM)Hmgu>/Hecw1<tm2b(EUCOMM)Hmgu>	C57BL/6N-Hecw1<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262614	M	MP:0001303	abnormal lens morphology	Herc1<em2(IMPC)Wtsi>/Herc1<em2(IMPC)Wtsi>	C57BL/6N-Herc1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262614	M	MP:0001304	cataract	Herc1<em2(IMPC)Wtsi>/Herc1<em2(IMPC)Wtsi>	C57BL/6N-Herc1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262615	M	MP:0002968	increased circulating alkaline phosphatase level	Herc1<em3(IMPC)Wtsi>/Herc1<em3(IMPC)Wtsi>	C57BL/6N-Herc1<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262615	F	MP:0001325	abnormal retina morphology	Herc1<em3(IMPC)Wtsi>/Herc1<em3(IMPC)Wtsi>	C57BL/6N-Herc1<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262615	M	MP:0002079	increased circulating insulin level	Herc1<em3(IMPC)Wtsi>/Herc1<em3(IMPC)Wtsi>	C57BL/6N-Herc1<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262615	M	MP:0001925	male infertility	Herc1<em3(IMPC)Wtsi>/Herc1<em3(IMPC)Wtsi>	C57BL/6N-Herc1<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262615	F	MP:0000218	increased leukocyte cell number	Herc1<em3(IMPC)Wtsi>/Herc1<em3(IMPC)Wtsi>	C57BL/6N-Herc1<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262615	F	MP:0008806	increased circulating amylase level	Herc1<em3(IMPC)Wtsi>/Herc1<em3(IMPC)Wtsi>	C57BL/6N-Herc1<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262615	F	MP:0000220	increased monocyte cell number	Herc1<em3(IMPC)Wtsi>/Herc1<em3(IMPC)Wtsi>	C57BL/6N-Herc1<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262615	M	MP:0005293	impaired glucose tolerance	Herc1<em3(IMPC)Wtsi>/Herc1<em3(IMPC)Wtsi>	C57BL/6N-Herc1<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262615	F	MP:0013022	increased Ly6C high monocyte number	Herc1<em3(IMPC)Wtsi>/Herc1<em3(IMPC)Wtsi>	C57BL/6N-Herc1<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262615	F	MP:0005011	increased eosinophil cell number	Herc1<em3(IMPC)Wtsi>/Herc1<em3(IMPC)Wtsi>	C57BL/6N-Herc1<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262616	F	MP:0001488	increased startle reflex	Herpud2<tm1.1(KOMP)Vlcg>/Herpud2<tm1.1(KOMP)Vlcg>	C57BL/6N-Herpud2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262617	M	MP:0001406	abnormal gait	Hexb<tm1b(EUCOMM)Hmgu>/Hexb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hexb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262617	F	MP:0010088	decreased circulating fructosamine level	Hexb<tm1b(EUCOMM)Hmgu>/Hexb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hexb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262617	M	MP:0001392	abnormal locomotor behavior	Hexb<tm1b(EUCOMM)Hmgu>/Hexb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hexb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262617	M	MP:0000745	tremors	Hexb<tm1b(EUCOMM)Hmgu>/Hexb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hexb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262617	M	MP:0001417	decreased exploration in new environment	Hexb<tm1b(EUCOMM)Hmgu>/Hexb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hexb<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262618	M	MP:0002764	short tibia	Hgsnat<em4(IMPC)Tcp>/Hgsnat<em4(IMPC)Tcp>	C57BL/6NCrl-Hgsnat<em4(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262618	M	MP:0010123	increased bone mineral content	Hgsnat<em4(IMPC)Tcp>/Hgsnat<em4(IMPC)Tcp>	C57BL/6NCrl-Hgsnat<em4(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262618	M	MP:0010025	decreased total body fat amount	Hgsnat<em4(IMPC)Tcp>/Hgsnat<em4(IMPC)Tcp>	C57BL/6NCrl-Hgsnat<em4(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262618	M	MP:0001566	increased circulating phosphate level	Hgsnat<em4(IMPC)Tcp>/Hgsnat<em4(IMPC)Tcp>	C57BL/6NCrl-Hgsnat<em4(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262618	M	MP:0001417	decreased exploration in new environment	Hgsnat<em4(IMPC)Tcp>/Hgsnat<em4(IMPC)Tcp>	C57BL/6NCrl-Hgsnat<em4(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262618	M	MP:0001488	increased startle reflex	Hgsnat<em4(IMPC)Tcp>/Hgsnat<em4(IMPC)Tcp>	C57BL/6NCrl-Hgsnat<em4(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262618	M	MP:0001175	abnormal lung morphology	Hgsnat<em4(IMPC)Tcp>/Hgsnat<em4(IMPC)Tcp>	C57BL/6NCrl-Hgsnat<em4(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262618	M	MP:0000702	enlarged lymph nodes	Hgsnat<em4(IMPC)Tcp>/Hgsnat<em4(IMPC)Tcp>	C57BL/6NCrl-Hgsnat<em4(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262618	M	MP:0003960	increased lean body mass	Hgsnat<em4(IMPC)Tcp>/Hgsnat<em4(IMPC)Tcp>	C57BL/6NCrl-Hgsnat<em4(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262618	M	MP:0005627	increased circulating potassium level	Hgsnat<em4(IMPC)Tcp>/Hgsnat<em4(IMPC)Tcp>	C57BL/6NCrl-Hgsnat<em4(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262618	M	MP:0002968	increased circulating alkaline phosphatase level	Hgsnat<em4(IMPC)Tcp>/Hgsnat<em4(IMPC)Tcp>	C57BL/6NCrl-Hgsnat<em4(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262618	M	MP:0011874	enlarged urinary bladder	Hgsnat<em4(IMPC)Tcp>/Hgsnat<em4(IMPC)Tcp>	C57BL/6NCrl-Hgsnat<em4(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262619	F	MP:0001417	decreased exploration in new environment	Hhatl<em1(IMPC)Mbp>/Hhatl<em1(IMPC)Mbp>	C57BL/6N-Hhatl<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262619	M	MP:0020421	increased freezing behavior	Hhatl<em1(IMPC)Mbp>/Hhatl<em1(IMPC)Mbp>	C57BL/6N-Hhatl<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262619	F	MP:0000063	decreased bone mineral density	Hhatl<em1(IMPC)Mbp>/Hhatl<em1(IMPC)Mbp>	C57BL/6N-Hhatl<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262619	M	MP:0011110	preweaning lethality, incomplete penetrance	Hhatl<em1(IMPC)Mbp>/Hhatl<em1(IMPC)Mbp>	C57BL/6N-Hhatl<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262620	F	MP:0011960	abnormal eye anterior chamber depth	Hibadh<tm1b(EUCOMM)Wtsi>/Hibadh<tm1b(EUCOMM)Wtsi>	C57BL/6N-Hibadh<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262620	F	MP:0003733	abnormal retina inner nuclear layer morphology	Hibadh<tm1b(EUCOMM)Wtsi>/Hibadh<tm1b(EUCOMM)Wtsi>	C57BL/6N-Hibadh<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262620	F	MP:0011239	abnormal skin coloration	Hibadh<tm1b(EUCOMM)Wtsi>/Hibadh<tm1b(EUCOMM)Wtsi>	C57BL/6N-Hibadh<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262621	F	MP:0000274	enlarged heart	Higd2a<tm1.1(KOMP)Vlcg>/Higd2a<+>	C57BL/6N-Higd2a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262621	F	MP:0000266	abnormal heart morphology	Higd2a<tm1.1(KOMP)Vlcg>/Higd2a<+>	C57BL/6N-Higd2a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262624	M	MP:0009142	decreased prepulse inhibition	Hipk3<tm1b(EUCOMM)Hmgu>/Hipk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hipk3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262624	F	MP:0005505	thrombocytosis	Hipk3<tm1b(EUCOMM)Hmgu>/Hipk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hipk3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262624	M	MP:0002599	increased mean platelet volume	Hipk3<tm1b(EUCOMM)Hmgu>/Hipk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hipk3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262624	M	MP:0001489	decreased startle reflex	Hipk3<tm1b(EUCOMM)Hmgu>/Hipk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hipk3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262624	M	MP:0013279	increased fasting circulating glucose level	Hipk3<tm1b(EUCOMM)Hmgu>/Hipk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hipk3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262624	M	MP:0010506	prolonged RR interval	Hipk3<tm1b(EUCOMM)Hmgu>/Hipk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hipk3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262624	M	MP:0005333	decreased heart rate	Hipk3<tm1b(EUCOMM)Hmgu>/Hipk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hipk3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262624	M	MP:0002941	increased circulating alanine transaminase level	Hipk3<tm1b(EUCOMM)Hmgu>/Hipk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hipk3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262624	M	MP:0003928	increased heart rate variability	Hipk3<tm1b(EUCOMM)Hmgu>/Hipk3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hipk3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262625	M	MP:0002965	increased circulating serum albumin level	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	C57BL/6N-Hipk4<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6262625	M	MP:0005566	decreased blood urea nitrogen level	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	C57BL/6N-Hipk4<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6262625	M	MP:0001513	limb grasping	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	C57BL/6N-Hipk4<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6262625	M	MP:0001925	male infertility	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	C57BL/6N-Hipk4<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6262625	M	MP:0001523	impaired righting response	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	C57BL/6N-Hipk4<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6262625	M	MP:0002075	abnormal coat/hair pigmentation	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	C57BL/6N-Hipk4<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6262628	M	MP:0002699	abnormal vitreous body morphology	Hmbs<tm1b(EUCOMM)Hmgu>/Hmbs<+>	C57BL/6N-Hmbs<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262628	M	MP:0001488	increased startle reflex	Hmbs<tm1b(EUCOMM)Hmgu>/Hmbs<+>	C57BL/6N-Hmbs<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262628	M	MP:0001303	abnormal lens morphology	Hmbs<tm1b(EUCOMM)Hmgu>/Hmbs<+>	C57BL/6N-Hmbs<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262628	F	MP:0001399	hyperactivity	Hmbs<tm1b(EUCOMM)Hmgu>/Hmbs<+>	C57BL/6N-Hmbs<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262630	F	MP:0001399	hyperactivity	Hmcn1<em1(IMPC)J>/Hmcn1<em1(IMPC)J>	C57BL/6NJ-Hmcn1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262630	F	MP:0001304	cataract	Hmcn1<em1(IMPC)J>/Hmcn1<em1(IMPC)J>	C57BL/6NJ-Hmcn1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262631	M	MP:0002608	increased hematocrit	Hmcn2<tm1b(EUCOMM)Wtsi>/Hmcn2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Hmcn2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262632	F	MP:0001914	hemorrhage	Hmg20a<em1(IMPC)J>/Hmg20a<em1(IMPC)J>	C57BL/6NJ-Hmg20a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262633	M	MP:0001697	abnormal embryo size	Hmgn2<tm1b(KOMP)Wtsi>/Hmgn2<tm1b(KOMP)Wtsi>	C57BL/6N-Hmgn2<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6262634	M	MP:0001262	decreased body weight	Hnf4a<tm1b(EUCOMM)Hmgu>/Hnf4a<+>	C57BL/6N-Hnf4a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262634	F	MP:0001289	persistence of hyaloid vascular system	Hnf4a<tm1b(EUCOMM)Hmgu>/Hnf4a<+>	C57BL/6N-Hnf4a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262634	M	MP:0005292	improved glucose tolerance	Hnf4a<tm1b(EUCOMM)Hmgu>/Hnf4a<+>	C57BL/6N-Hnf4a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262634	M	MP:0001556	increased circulating HDL cholesterol level	Hnf4a<tm1b(EUCOMM)Hmgu>/Hnf4a<+>	C57BL/6N-Hnf4a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262634	M	MP:0005178	increased circulating cholesterol level	Hnf4a<tm1b(EUCOMM)Hmgu>/Hnf4a<+>	C57BL/6N-Hnf4a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262634	F	MP:0005344	increased circulating bilirubin level	Hnf4a<tm1b(EUCOMM)Hmgu>/Hnf4a<+>	C57BL/6N-Hnf4a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262636	F	MP:0005419	decreased circulating serum albumin level	Hnrnpc<tm1b(EUCOMM)Hmgu>/Hnrnpc<+>	C57BL/6N-Hnrnpc<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262636	M	MP:0005292	improved glucose tolerance	Hnrnpc<tm1b(EUCOMM)Hmgu>/Hnrnpc<+>	C57BL/6N-Hnrnpc<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262640	M	MP:0000266	abnormal heart morphology	Hoxa10<tm1.1(KOMP)Vlcg>/Hoxa10<tm1.1(KOMP)Vlcg>	C57BL/6N-Hoxa10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262640	M	MP:0000274	enlarged heart	Hoxa10<tm1.1(KOMP)Vlcg>/Hoxa10<tm1.1(KOMP)Vlcg>	C57BL/6N-Hoxa10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262641	F	MP:0009142	decreased prepulse inhibition	Hoxa2<tm1b(EUCOMM)Wtsi>/Hoxa2<+>	C57BL/6N-Hoxa2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262641	F	MP:0010379	decreased respiratory quotient	Hoxa2<tm1b(EUCOMM)Wtsi>/Hoxa2<+>	C57BL/6N-Hoxa2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262641	M	MP:0001406	abnormal gait	Hoxa2<tm1b(EUCOMM)Wtsi>/Hoxa2<+>	C57BL/6N-Hoxa2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262645	M	MP:0010067	increased red blood cell distribution width	Hpf1<em1(IMPC)Wtsi>/Hpf1<em1(IMPC)Wtsi>	C57BL/6N-Hpf1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262645	M	MP:0000572	abnormal autopod morphology	Hpf1<em1(IMPC)Wtsi>/Hpf1<em1(IMPC)Wtsi>	C57BL/6N-Hpf1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262646	M	MP:0000266	abnormal heart morphology	Hpgds<tm1b(KOMP)Wtsi>/Hpgds<tm1b(KOMP)Wtsi>	C57BL/6N-Hpgds<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262646	M	MP:0000274	enlarged heart	Hpgds<tm1b(KOMP)Wtsi>/Hpgds<tm1b(KOMP)Wtsi>	C57BL/6N-Hpgds<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262647	M	MP:0006243	impaired pupillary reflex	Hpse2<em1(IMPC)J>/Hpse2<+>	C57BL/6NJ-Hpse2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262647	F	MP:0001304	cataract	Hpse2<em1(IMPC)J>/Hpse2<+>	C57BL/6NJ-Hpse2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262651	F	MP:0010053	decreased grip strength	Hsbp1l1<em1(IMPC)J>/Hsbp1l1<em1(IMPC)J>	C57BL/6NJ-Hsbp1l1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262651	M	MP:0006243	impaired pupillary reflex	Hsbp1l1<em1(IMPC)J>/Hsbp1l1<em1(IMPC)J>	C57BL/6NJ-Hsbp1l1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262651	M	MP:0001289	persistence of hyaloid vascular system	Hsbp1l1<em1(IMPC)J>/Hsbp1l1<em1(IMPC)J>	C57BL/6NJ-Hsbp1l1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262652	F	MP:0000689	abnormal spleen morphology	Hsd17b4<em1(IMPC)Tcp>/Hsd17b4<em1(IMPC)Tcp>	C57BL/6NCrl-Hsd17b4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262652	M	MP:0001304	cataract	Hsd17b4<em1(IMPC)Tcp>/Hsd17b4<em1(IMPC)Tcp>	C57BL/6NCrl-Hsd17b4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262652	F	MP:0002092	abnormal eye morphology	Hsd17b4<em1(IMPC)Tcp>/Hsd17b4<em1(IMPC)Tcp>	C57BL/6NCrl-Hsd17b4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262652	F	MP:0000642	enlarged adrenal glands	Hsd17b4<em1(IMPC)Tcp>/Hsd17b4<em1(IMPC)Tcp>	C57BL/6NCrl-Hsd17b4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262652	F	MP:0000157	abnormal sternum morphology	Hsd17b4<em1(IMPC)Tcp>/Hsd17b4<em1(IMPC)Tcp>	C57BL/6NCrl-Hsd17b4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262652	F	MP:0002637	small uterus	Hsd17b4<em1(IMPC)Tcp>/Hsd17b4<em1(IMPC)Tcp>	C57BL/6NCrl-Hsd17b4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262652	F	MP:0001319	irregularly shaped pupil	Hsd17b4<em1(IMPC)Tcp>/Hsd17b4<em1(IMPC)Tcp>	C57BL/6NCrl-Hsd17b4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262653	M	MP:0002941	increased circulating alanine transaminase level	Hsf4<tm1b(KOMP)Wtsi>/Hsf4<tm1b(KOMP)Wtsi>	C57BL/6N-Hsf4<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262656	F	MP:0003019	increased circulating chloride level	Htr7<tm1b(KOMP)Wtsi>/Htr7<tm1b(KOMP)Wtsi>	C57BL/6N-Htr7<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262656	M	MP:0013278	decreased fasting circulating glucose level	Htr7<tm1b(KOMP)Wtsi>/Htr7<tm1b(KOMP)Wtsi>	C57BL/6N-Htr7<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262657	M	MP:0002110	abnormal digit morphology	Hunk<tm1b(EUCOMM)Wtsi>/Hunk<tm1b(EUCOMM)Wtsi>	C57BL/6N-Hunk<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262657	M	MP:0005559	increased circulating glucose level	Hunk<tm1b(EUCOMM)Wtsi>/Hunk<tm1b(EUCOMM)Wtsi>	C57BL/6N-Hunk<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262658	F	MP:0009142	decreased prepulse inhibition	Hyls1<em1(IMPC)Tcp>/Hyls1<+>	C57BL/6NCrl-Hyls1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262658	M	MP:0011953	prolonged PQ interval	Hyls1<em1(IMPC)Tcp>/Hyls1<+>	C57BL/6NCrl-Hyls1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262660	F	MP:0002092	abnormal eye morphology	Iars2<em1(IMPC)Tcp>/Iars2<+>	C57BL/6NCrl-Iars2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262662	M	MP:0002092	abnormal eye morphology	Ica1l<tm1b(EUCOMM)Hmgu>/Ica1l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ica1l<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262662	M	MP:0000274	enlarged heart	Ica1l<tm1b(EUCOMM)Hmgu>/Ica1l<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ica1l<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262663	M	MP:0003068	enlarged kidney	Ica1<tm1b(EUCOMM)Wtsi>/Ica1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ica1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262663	M	MP:0000689	abnormal spleen morphology	Ica1<tm1b(EUCOMM)Wtsi>/Ica1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ica1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262663	F	MP:0001402	decreased locomotor activity	Ica1<tm1b(EUCOMM)Wtsi>/Ica1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ica1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262663	M	MP:0002135	abnormal kidney morphology	Ica1<tm1b(EUCOMM)Wtsi>/Ica1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ica1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262663	M	MP:0002092	abnormal eye morphology	Ica1<tm1b(EUCOMM)Wtsi>/Ica1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ica1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262663	M	MP:0000692	small spleen	Ica1<tm1b(EUCOMM)Wtsi>/Ica1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ica1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262664	M	MP:0002098	abnormal vibrissa morphology	Icam5<em1(IMPC)Wtsi>/Icam5<em1(IMPC)Wtsi>	C57BL/6N-Icam5<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262665	M	MP:0002764	short tibia	Icos<tm2b(EUCOMM)Wtsi>/Icos<tm2b(EUCOMM)Wtsi>	C57BL/6N-Icos<tm2b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262666	F	MP:0005553	increased circulating creatinine level	Id2<tm2b(EUCOMM)Wtsi>/Id2<+>	C57BL/6N-Id2<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262666	F	MP:0005565	increased blood urea nitrogen level	Id2<tm2b(EUCOMM)Wtsi>/Id2<+>	C57BL/6N-Id2<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262667	M	MP:0005564	increased hemoglobin content	Idh2<tm1b(EUCOMM)Hmgu>/Idh2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Idh2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262667	M	MP:0002591	decreased mean corpuscular volume	Idh2<tm1b(EUCOMM)Hmgu>/Idh2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Idh2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262669	M	MP:0011999	abnormal tail length	Ifi27l2a<tm1.1(KOMP)Vlcg>/Ifi27l2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Ifi27l2a<tm1.1(KOMP)Vlcg>/Ieg	N	MGI:5576271
MGI:6262669	M	MP:0005344	increased circulating bilirubin level	Ifi27l2a<tm1.1(KOMP)Vlcg>/Ifi27l2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Ifi27l2a<tm1.1(KOMP)Vlcg>/Ieg	N	MGI:5576271
MGI:6262669	M	MP:0001312	abnormal cornea morphology	Ifi27l2a<tm1.1(KOMP)Vlcg>/Ifi27l2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Ifi27l2a<tm1.1(KOMP)Vlcg>/Ieg	N	MGI:5576271
MGI:6262669	M	MP:0010097	abnormal retina blood vessel morphology	Ifi27l2a<tm1.1(KOMP)Vlcg>/Ifi27l2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Ifi27l2a<tm1.1(KOMP)Vlcg>/Ieg	N	MGI:5576271
MGI:6262669	F	MP:0002968	increased circulating alkaline phosphatase level	Ifi27l2a<tm1.1(KOMP)Vlcg>/Ifi27l2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Ifi27l2a<tm1.1(KOMP)Vlcg>/Ieg	N	MGI:5576271
MGI:6262669	F	MP:0002792	abnormal retina vasculature morphology	Ifi27l2a<tm1.1(KOMP)Vlcg>/Ifi27l2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Ifi27l2a<tm1.1(KOMP)Vlcg>/Ieg	N	MGI:5576271
MGI:6262670	M	MP:0010052	increased grip strength	Ifi27<tm1b(EUCOMM)Wtsi>/Ifi27<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ifi27<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262671	M	MP:0004357	long tibia	Ifitm1<tm1b(EUCOMM)Wtsi>/Ifitm1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ifitm1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262671	M	MP:0000443	abnormal snout morphology	Ifitm1<tm1b(EUCOMM)Wtsi>/Ifitm1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ifitm1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6262672	F	MP:0002110	abnormal digit morphology	Ift172<tm2b(EUCOMM)Hmgu>/Ift172<+>	C57BL/6N-Ift172<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262672	M	MP:0010097	abnormal retina blood vessel morphology	Ift172<tm2b(EUCOMM)Hmgu>/Ift172<+>	C57BL/6N-Ift172<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262675	F	MP:0000266	abnormal heart morphology	Ift43<tm1b(EUCOMM)Hmgu>/Ift43<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ift43<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262675	F	MP:0000269	abnormal heart looping	Ift43<tm1b(EUCOMM)Hmgu>/Ift43<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ift43<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262676	F	MP:0001488	increased startle reflex	Ift81<tm1b(EUCOMM)Wtsi>/Ift81<+>	C57BL/6N-Ift81<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262678	F	MP:0005178	increased circulating cholesterol level	Igfals<tm1b(KOMP)Wtsi>/Igfals<tm1b(KOMP)Wtsi>	C57BL/6N-Igfals<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262678	F	MP:0005278	abnormal cholesterol homeostasis	Igfals<tm1b(KOMP)Wtsi>/Igfals<tm1b(KOMP)Wtsi>	C57BL/6N-Igfals<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262679	F	MP:0001102	small superior vagus ganglion	Igflr1<tm1b(KOMP)Mbp>/Igflr1<tm1b(KOMP)Mbp>	C57BL/6N-Igflr1<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6262679	F	MP:0009709	hydrometra	Igflr1<tm1b(KOMP)Mbp>/Igflr1<tm1b(KOMP)Mbp>	C57BL/6N-Igflr1<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6262680	M	MP:0010124	decreased bone mineral content	Ighmbp2<em1(IMPC)Tcp>/Ighmbp2<+>	C57BL/6NCrl-Ighmbp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262680	F	MP:0002060	abnormal skin morphology	Ighmbp2<em1(IMPC)Tcp>/Ighmbp2<+>	C57BL/6NCrl-Ighmbp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262680	M	MP:0003068	enlarged kidney	Ighmbp2<em1(IMPC)Tcp>/Ighmbp2<+>	C57BL/6NCrl-Ighmbp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262682	M	MP:0005293	impaired glucose tolerance	Igsf8<em1(IMPC)Wtsi>/Igsf8<em1(IMPC)Wtsi>	C57BL/6N-Igsf8<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262685	M	MP:0005292	improved glucose tolerance	Il10ra<tm1b(KOMP)Wtsi>/Il10ra<tm1b(KOMP)Wtsi>	C57BL/6N-Il10ra<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6262686	F	MP:0005628	decreased circulating potassium level	Il13ra2<tm1b(EUCOMM)Hmgu>/Il13ra2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il13ra2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262688	F	MP:0010506	prolonged RR interval	Il18r1<em1(IMPC)Mbp>/Il18r1<em1(IMPC)Mbp>	C57BL/6N-Il18r1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262688	F	MP:0005333	decreased heart rate	Il18r1<em1(IMPC)Mbp>/Il18r1<em1(IMPC)Mbp>	C57BL/6N-Il18r1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262689	F	MP:0002073	abnormal hair growth	Il18rap<em1(IMPC)Wtsi>/Il18rap<em1(IMPC)Wtsi>	C57BL/6N-Il18rap<em1(IMPC)Wtsi>/WtsiCnrm	N	MGI:5576271
MGI:6262690	M	MP:0004931	enlarged epididymis	Il20rb<em2(IMPC)Mbp>/Il20rb<em2(IMPC)Mbp>	C57BL/6N-Il20rb<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262690	F	MP:0001102	small superior vagus ganglion	Il20rb<em2(IMPC)Mbp>/Il20rb<em2(IMPC)Mbp>	C57BL/6N-Il20rb<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262690	M	MP:0000266	abnormal heart morphology	Il20rb<em2(IMPC)Mbp>/Il20rb<em2(IMPC)Mbp>	C57BL/6N-Il20rb<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262690	F	MP:0002941	increased circulating alanine transaminase level	Il20rb<em2(IMPC)Mbp>/Il20rb<em2(IMPC)Mbp>	C57BL/6N-Il20rb<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262690	M	MP:0002631	abnormal epididymis morphology	Il20rb<em2(IMPC)Mbp>/Il20rb<em2(IMPC)Mbp>	C57BL/6N-Il20rb<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262690	M	MP:0000274	enlarged heart	Il20rb<em2(IMPC)Mbp>/Il20rb<em2(IMPC)Mbp>	C57BL/6N-Il20rb<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262690	F	MP:0009709	hydrometra	Il20rb<em2(IMPC)Mbp>/Il20rb<em2(IMPC)Mbp>	C57BL/6N-Il20rb<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262692	M	MP:0010836	decreased CD4-positive, alpha-beta memory T cell number	Il27<tm1b(EUCOMM)Wtsi>/Il27<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il27<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262693	F	MP:0001469	abnormal contextual conditioning behavior	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0003271	abnormal duodenum morphology	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	F	MP:0002757	decreased vertical activity	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0002834	decreased heart weight	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0002875	decreased erythrocyte cell number	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0002591	decreased mean corpuscular volume	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	F	MP:0000137	abnormal vertebrae morphology	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	F	MP:0005343	increased circulating aspartate transaminase level	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	F	MP:0005566	decreased blood urea nitrogen level	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	F	MP:0020420	abnormal freezing behavior	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0005292	improved glucose tolerance	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	F	MP:0005560	decreased circulating glucose level	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0003896	prolonged PR interval	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0012362	increased large unstained cell number	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0000219	increased neutrophil cell number	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0005016	decreased lymphocyte cell number	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0001258	decreased body length	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0002874	decreased hemoglobin content	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0000063	decreased bone mineral density	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0000208	decreased hematocrit	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	F	MP:0005179	decreased circulating cholesterol level	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	F	MP:0005278	abnormal cholesterol homeostasis	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0001566	increased circulating phosphate level	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0005562	decreased mean corpuscular hemoglobin	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262693	M	MP:0000495	abnormal colon morphology	Il2ra<tm1b(EUCOMM)Wtsi>/Il2ra<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il2ra<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262694	M	MP:0002102	abnormal ear morphology	Il2rb<tm1b(EUCOMM)Hmgu>/Il2rb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il2rb<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6262694	F	MP:0001926	female infertility	Il2rb<tm1b(EUCOMM)Hmgu>/Il2rb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il2rb<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6262694	M	MP:0001925	male infertility	Il2rb<tm1b(EUCOMM)Hmgu>/Il2rb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Il2rb<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6262695	M	MP:0002764	short tibia	Il31<tm1b(EUCOMM)Wtsi>/Il31<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il31<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262696	M	MP:0010124	decreased bone mineral content	Il3<tm1.1(KOMP)Mbp>/Il3<tm1.1(KOMP)Mbp>	C57BL/6N-Il3<tm1.1(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6262696	M	MP:0001925	male infertility	Il3<tm1.1(KOMP)Mbp>/Il3<tm1.1(KOMP)Mbp>	C57BL/6N-Il3<tm1.1(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6262696	F	MP:0001926	female infertility	Il3<tm1.1(KOMP)Mbp>/Il3<tm1.1(KOMP)Mbp>	C57BL/6N-Il3<tm1.1(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6262697	F	MP:0002590	increased mean corpuscular volume	Ing2<tm1.1(KOMP)Vlcg>/Ing2<+>	C57BL/6N-Ing2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262697	F	MP:0002941	increased circulating alanine transaminase level	Ing2<tm1.1(KOMP)Vlcg>/Ing2<+>	C57BL/6N-Ing2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262697	F	MP:0005344	increased circulating bilirubin level	Ing2<tm1.1(KOMP)Vlcg>/Ing2<+>	C57BL/6N-Ing2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262697	M	MP:0001399	hyperactivity	Ing2<tm1.1(KOMP)Vlcg>/Ing2<+>	C57BL/6N-Ing2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262700	F	MP:0003984	embryonic growth retardation	Ino80d<tm1b(EUCOMM)Wtsi>/Ino80d<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ino80d<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262700	F	MP:0001697	abnormal embryo size	Ino80d<tm1b(EUCOMM)Wtsi>/Ino80d<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ino80d<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262701	F	MP:0005554	decreased circulating creatinine level	Ints10<tm1b(KOMP)Wtsi>/Ints10<+>	C57BL/6N-Ints10<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262701	M	MP:0006243	impaired pupillary reflex	Ints10<tm1b(KOMP)Wtsi>/Ints10<+>	C57BL/6N-Ints10<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262702	F	MP:0000266	abnormal heart morphology	Ints10<tm1b(KOMP)Wtsi>/Ints10<tm1b(KOMP)Wtsi>	C57BL/6N-Ints10<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262705	F	MP:0005562	decreased mean corpuscular hemoglobin	Ints9<tm1b(KOMP)Wtsi>/Ints9<+>	C57BL/6N-Ints9<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262705	M	MP:0008806	increased circulating amylase level	Ints9<tm1b(KOMP)Wtsi>/Ints9<+>	C57BL/6N-Ints9<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262705	M	MP:0005565	increased blood urea nitrogen level	Ints9<tm1b(KOMP)Wtsi>/Ints9<+>	C57BL/6N-Ints9<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262708	M	MP:0001417	decreased exploration in new environment	Ipo8<tm1.1(KOMP)Vlcg>/Ipo8<tm1.1(KOMP)Vlcg>	C57BL/6N-Ipo8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262709	M	MP:0011954	shortened PQ interval	Iqca1<em1(IMPC)J>/Iqca1<em1(IMPC)J>	C57BL/6NJ-Iqca1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262709	M	MP:0010511	shortened PR interval	Iqca1<em1(IMPC)J>/Iqca1<em1(IMPC)J>	C57BL/6NJ-Iqca1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262709	M	MP:0002941	increased circulating alanine transaminase level	Iqca1<em1(IMPC)J>/Iqca1<em1(IMPC)J>	C57BL/6NJ-Iqca1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262709	F	MP:0001488	increased startle reflex	Iqca1<em1(IMPC)J>/Iqca1<em1(IMPC)J>	C57BL/6NJ-Iqca1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262710	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Iqcj<em1(IMPC)J>/Iqcj<em1(IMPC)J>	C57BL/6NJ-Iqcj<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262710	M	MP:0002590	increased mean corpuscular volume	Iqcj<em1(IMPC)J>/Iqcj<em1(IMPC)J>	C57BL/6NJ-Iqcj<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262711	F	MP:0000063	decreased bone mineral density	Iqgap1<tm1b(EUCOMM)Wtsi>/Iqgap1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Iqgap1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262711	M	MP:0010052	increased grip strength	Iqgap1<tm1b(EUCOMM)Wtsi>/Iqgap1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Iqgap1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6262712	M	MP:0001488	increased startle reflex	Iqgap2<tm1b(KOMP)Wtsi>/Iqgap2<tm1b(KOMP)Wtsi>	C57BL/6N-Iqgap2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262713	M	MP:0003960	increased lean body mass	Irgm1<em1(IMPC)Wtsi>/Irgm1<em1(IMPC)Wtsi>	C57BL/6N-Irgm1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262713	M	MP:0013278	decreased fasting circulating glucose level	Irgm1<em1(IMPC)Wtsi>/Irgm1<em1(IMPC)Wtsi>	C57BL/6N-Irgm1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262713	M	MP:0005419	decreased circulating serum albumin level	Irgm1<em1(IMPC)Wtsi>/Irgm1<em1(IMPC)Wtsi>	C57BL/6N-Irgm1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262713	M	MP:0005343	increased circulating aspartate transaminase level	Irgm1<em1(IMPC)Wtsi>/Irgm1<em1(IMPC)Wtsi>	C57BL/6N-Irgm1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262713	M	MP:0005292	improved glucose tolerance	Irgm1<em1(IMPC)Wtsi>/Irgm1<em1(IMPC)Wtsi>	C57BL/6N-Irgm1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262713	M	MP:0002875	decreased erythrocyte cell number	Irgm1<em1(IMPC)Wtsi>/Irgm1<em1(IMPC)Wtsi>	C57BL/6N-Irgm1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262713	F	MP:0000182	increased circulating LDL cholesterol level	Irgm1<em1(IMPC)Wtsi>/Irgm1<em1(IMPC)Wtsi>	C57BL/6N-Irgm1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262713	F	MP:0005178	increased circulating cholesterol level	Irgm1<em1(IMPC)Wtsi>/Irgm1<em1(IMPC)Wtsi>	C57BL/6N-Irgm1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262713	M	MP:0002092	abnormal eye morphology	Irgm1<em1(IMPC)Wtsi>/Irgm1<em1(IMPC)Wtsi>	C57BL/6N-Irgm1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262714	M	MP:0001510	abnormal coat appearance	Irgm2<em1(IMPC)J>/Irgm2<em1(IMPC)J>	C57BL/6NJ-Irgm2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262714	F	MP:0001486	abnormal startle reflex	Irgm2<em1(IMPC)J>/Irgm2<em1(IMPC)J>	C57BL/6NJ-Irgm2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262714	F	MP:0001303	abnormal lens morphology	Irgm2<em1(IMPC)J>/Irgm2<em1(IMPC)J>	C57BL/6NJ-Irgm2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262714	F	MP:0002060	abnormal skin morphology	Irgm2<em1(IMPC)J>/Irgm2<em1(IMPC)J>	C57BL/6NJ-Irgm2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262714	M	MP:0020870	decreased thigmotaxis	Irgm2<em1(IMPC)J>/Irgm2<em1(IMPC)J>	C57BL/6NJ-Irgm2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262715	M	MP:0001402	decreased locomotor activity	Irx1<tm1.1(KOMP)Vlcg>/Irx1<+>	C57BL/6N-Irx1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262715	M	MP:0020870	decreased thigmotaxis	Irx1<tm1.1(KOMP)Vlcg>/Irx1<+>	C57BL/6N-Irx1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262716	F	MP:0013278	decreased fasting circulating glucose level	Irx3<em2(IMPC)H>/Irx3<em2(IMPC)H>	C57BL/6N-Irx3<em2(IMPC)H>/H	N	MGI:5576271
MGI:6262716	M	MP:0010124	decreased bone mineral content	Irx3<em2(IMPC)H>/Irx3<em2(IMPC)H>	C57BL/6N-Irx3<em2(IMPC)H>/H	N	MGI:5576271
MGI:6262716	F	MP:0010052	increased grip strength	Irx3<em2(IMPC)H>/Irx3<em2(IMPC)H>	C57BL/6N-Irx3<em2(IMPC)H>/H	N	MGI:5576271
MGI:6262716	M	MP:0000443	abnormal snout morphology	Irx3<em2(IMPC)H>/Irx3<em2(IMPC)H>	C57BL/6N-Irx3<em2(IMPC)H>/H	N	MGI:5576271
MGI:6262716	F	MP:0001312	abnormal cornea morphology	Irx3<em2(IMPC)H>/Irx3<em2(IMPC)H>	C57BL/6N-Irx3<em2(IMPC)H>/H	N	MGI:5576271
MGI:6262717	M	MP:0011110	preweaning lethality, incomplete penetrance	Itih4<tm3b(KOMP)Wtsi>/Itih4<tm3b(KOMP)Wtsi>	C57BL/6N-Itih4<tm3b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262719	F	MP:0001926	female infertility	Jade1<tm1b(KOMP)Wtsi>/Jade1<tm1b(KOMP)Wtsi>	C57BL/6N-Jade1<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262719	M	MP:0001925	male infertility	Jade1<tm1b(KOMP)Wtsi>/Jade1<tm1b(KOMP)Wtsi>	C57BL/6N-Jade1<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262725	M	MP:0005293	impaired glucose tolerance	Kat2b<em1(IMPC)Wtsi>/Kat2b<em1(IMPC)Wtsi>	C57BL/6N-Kat2b<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262725	M	MP:0005179	decreased circulating cholesterol level	Kat2b<em1(IMPC)Wtsi>/Kat2b<em1(IMPC)Wtsi>	C57BL/6N-Kat2b<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262725	M	MP:0010067	increased red blood cell distribution width	Kat2b<em1(IMPC)Wtsi>/Kat2b<em1(IMPC)Wtsi>	C57BL/6N-Kat2b<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262725	M	MP:0000186	decreased circulating HDL cholesterol level	Kat2b<em1(IMPC)Wtsi>/Kat2b<em1(IMPC)Wtsi>	C57BL/6N-Kat2b<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6262728	F	MP:0005344	increased circulating bilirubin level	Kbtbd7<tm1.1(KOMP)Vlcg>/Kbtbd7<tm1.1(KOMP)Vlcg>	C57BL/6N-Kbtbd7<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262728	F	MP:0003795	abnormal bone structure	Kbtbd7<tm1.1(KOMP)Vlcg>/Kbtbd7<tm1.1(KOMP)Vlcg>	C57BL/6N-Kbtbd7<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262728	F	MP:0010124	decreased bone mineral content	Kbtbd7<tm1.1(KOMP)Vlcg>/Kbtbd7<tm1.1(KOMP)Vlcg>	C57BL/6N-Kbtbd7<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262729	M	MP:0000689	abnormal spleen morphology	Kcna10<em3(IMPC)Mbp>/Kcna10<+>	C57BL/6N-Kcna10<em3(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262729	M	MP:0000266	abnormal heart morphology	Kcna10<em3(IMPC)Mbp>/Kcna10<+>	C57BL/6N-Kcna10<em3(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262729	M	MP:0000274	enlarged heart	Kcna10<em3(IMPC)Mbp>/Kcna10<+>	C57BL/6N-Kcna10<em3(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262729	M	MP:0000691	enlarged spleen	Kcna10<em3(IMPC)Mbp>/Kcna10<+>	C57BL/6N-Kcna10<em3(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262731	M	MP:0001148	enlarged testis	Kcnab3<tm1.1(KOMP)Vlcg>/Kcnab3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnab3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262731	F	MP:0002941	increased circulating alanine transaminase level	Kcnab3<tm1.1(KOMP)Vlcg>/Kcnab3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnab3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262731	F	MP:0005343	increased circulating aspartate transaminase level	Kcnab3<tm1.1(KOMP)Vlcg>/Kcnab3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnab3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262731	M	MP:0000274	enlarged heart	Kcnab3<tm1.1(KOMP)Vlcg>/Kcnab3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnab3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262731	M	MP:0000266	abnormal heart morphology	Kcnab3<tm1.1(KOMP)Vlcg>/Kcnab3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnab3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262731	F	MP:0005278	abnormal cholesterol homeostasis	Kcnab3<tm1.1(KOMP)Vlcg>/Kcnab3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnab3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262731	M	MP:0001146	abnormal testis morphology	Kcnab3<tm1.1(KOMP)Vlcg>/Kcnab3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnab3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262731	M	MP:0001175	abnormal lung morphology	Kcnab3<tm1.1(KOMP)Vlcg>/Kcnab3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnab3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262731	M	MP:0004882	enlarged lung	Kcnab3<tm1.1(KOMP)Vlcg>/Kcnab3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnab3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262732	F	MP:0005344	increased circulating bilirubin level	Kcnb2<em1(IMPC)J>/Kcnb2<em1(IMPC)J>	C57BL/6NJ-Kcnb2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262732	F	MP:0002875	decreased erythrocyte cell number	Kcnb2<em1(IMPC)J>/Kcnb2<em1(IMPC)J>	C57BL/6NJ-Kcnb2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262732	M	MP:0002941	increased circulating alanine transaminase level	Kcnb2<em1(IMPC)J>/Kcnb2<em1(IMPC)J>	C57BL/6NJ-Kcnb2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262732	F	MP:0000208	decreased hematocrit	Kcnb2<em1(IMPC)J>/Kcnb2<em1(IMPC)J>	C57BL/6NJ-Kcnb2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262733	M	MP:0010124	decreased bone mineral content	Kcnc3<em1(IMPC)J>/Kcnc3<em1(IMPC)J>	C57BL/6NJ-Kcnc3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262733	F	MP:0002574	increased vertical activity	Kcnc3<em1(IMPC)J>/Kcnc3<em1(IMPC)J>	C57BL/6NJ-Kcnc3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262733	M	MP:0010053	decreased grip strength	Kcnc3<em1(IMPC)J>/Kcnc3<em1(IMPC)J>	C57BL/6NJ-Kcnc3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262733	M	MP:0000063	decreased bone mineral density	Kcnc3<em1(IMPC)J>/Kcnc3<em1(IMPC)J>	C57BL/6NJ-Kcnc3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262734	F	MP:0005566	decreased blood urea nitrogen level	Kcnd3<em1(IMPC)J>/Kcnd3<em1(IMPC)J>	C57BL/6NJ-Kcnd3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262734	M	MP:0020870	decreased thigmotaxis	Kcnd3<em1(IMPC)J>/Kcnd3<em1(IMPC)J>	C57BL/6NJ-Kcnd3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262735	M	MP:0001891	hydrocephaly	Kcng4<tm1.1(KOMP)Vlcg>/Kcng4<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262735	F	MP:0005343	increased circulating aspartate transaminase level	Kcng4<tm1.1(KOMP)Vlcg>/Kcng4<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262735	M	MP:0002152	abnormal brain morphology	Kcng4<tm1.1(KOMP)Vlcg>/Kcng4<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262736	M	MP:0002997	enlarged seminal vesicle	Kcnh8<em1(IMPC)Mbp>/Kcnh8<em1(IMPC)Mbp>	C57BL/6N-Kcnh8<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262736	F	MP:0000691	enlarged spleen	Kcnh8<em1(IMPC)Mbp>/Kcnh8<em1(IMPC)Mbp>	C57BL/6N-Kcnh8<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262736	M	MP:0000598	abnormal liver morphology	Kcnh8<em1(IMPC)Mbp>/Kcnh8<em1(IMPC)Mbp>	C57BL/6N-Kcnh8<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262736	M	MP:0003642	absent seminal vesicle	Kcnh8<em1(IMPC)Mbp>/Kcnh8<em1(IMPC)Mbp>	C57BL/6N-Kcnh8<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262736	F	MP:0002060	abnormal skin morphology	Kcnh8<em1(IMPC)Mbp>/Kcnh8<em1(IMPC)Mbp>	C57BL/6N-Kcnh8<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262736	F	MP:0000689	abnormal spleen morphology	Kcnh8<em1(IMPC)Mbp>/Kcnh8<em1(IMPC)Mbp>	C57BL/6N-Kcnh8<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262736	F	MP:0009709	hydrometra	Kcnh8<em1(IMPC)Mbp>/Kcnh8<em1(IMPC)Mbp>	C57BL/6N-Kcnh8<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262736	F	MP:0002092	abnormal eye morphology	Kcnh8<em1(IMPC)Mbp>/Kcnh8<em1(IMPC)Mbp>	C57BL/6N-Kcnh8<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262736	F	MP:0001126	abnormal ovary morphology	Kcnh8<em1(IMPC)Mbp>/Kcnh8<em1(IMPC)Mbp>	C57BL/6N-Kcnh8<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262737	F	MP:0008935	decreased mean platelet volume	Kcnj10<tm1b(KOMP)Wtsi>/Kcnj10<+>	C57BL/6N-Kcnj10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262737	M	MP:0000745	tremors	Kcnj10<tm1b(KOMP)Wtsi>/Kcnj10<+>	C57BL/6N-Kcnj10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262737	F	MP:0002607	decreased basophil cell number	Kcnj10<tm1b(KOMP)Wtsi>/Kcnj10<+>	C57BL/6N-Kcnj10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262737	F	MP:0001488	increased startle reflex	Kcnj10<tm1b(KOMP)Wtsi>/Kcnj10<+>	C57BL/6N-Kcnj10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262739	M	MP:0010067	increased red blood cell distribution width	Kcnk13<em1(IMPC)H>/Kcnk13<em1(IMPC)H>	C57BL/6N-Kcnk13<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262739	M	MP:0002590	increased mean corpuscular volume	Kcnk13<em1(IMPC)H>/Kcnk13<em1(IMPC)H>	C57BL/6N-Kcnk13<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262740	F	MP:0001284	absent vibrissae	Kctd17<em1(IMPC)H>/Kctd17<em1(IMPC)H>	C57BL/6N-Kctd17<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262741	F	MP:0001552	increased circulating triglyceride level	Kctd1<em1(IMPC)J>/Kctd1<em1(IMPC)J>	C57BL/6NJ-Kctd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262741	M	MP:0002574	increased vertical activity	Kctd1<em1(IMPC)J>/Kctd1<em1(IMPC)J>	C57BL/6NJ-Kctd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262741	M	MP:0002834	decreased heart weight	Kctd1<em1(IMPC)J>/Kctd1<em1(IMPC)J>	C57BL/6NJ-Kctd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262741	F	MP:0001304	cataract	Kctd1<em1(IMPC)J>/Kctd1<em1(IMPC)J>	C57BL/6NJ-Kctd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262741	F	MP:0000218	increased leukocyte cell number	Kctd1<em1(IMPC)J>/Kctd1<em1(IMPC)J>	C57BL/6NJ-Kctd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262741	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Kctd1<em1(IMPC)J>/Kctd1<em1(IMPC)J>	C57BL/6NJ-Kctd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262741	F	MP:0005568	increased circulating total protein level	Kctd1<em1(IMPC)J>/Kctd1<em1(IMPC)J>	C57BL/6NJ-Kctd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262741	F	MP:0005344	increased circulating bilirubin level	Kctd1<em1(IMPC)J>/Kctd1<em1(IMPC)J>	C57BL/6NJ-Kctd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262741	F	MP:0000063	decreased bone mineral density	Kctd1<em1(IMPC)J>/Kctd1<em1(IMPC)J>	C57BL/6NJ-Kctd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262742	M	MP:0005561	increased mean corpuscular hemoglobin	Kctd9<em1(IMPC)J>/Kctd9<em1(IMPC)J>	C57BL/6NJ-Kctd9<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262742	M	MP:0002590	increased mean corpuscular volume	Kctd9<em1(IMPC)J>/Kctd9<em1(IMPC)J>	C57BL/6NJ-Kctd9<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262742	M	MP:0002574	increased vertical activity	Kctd9<em1(IMPC)J>/Kctd9<em1(IMPC)J>	C57BL/6NJ-Kctd9<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262745	M	MP:0005344	increased circulating bilirubin level	Keg1<tm1b(KOMP)Mbp>/Keg1<tm1b(KOMP)Mbp>	C57BL/6N-Keg1<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6262745	F	MP:0000194	increased circulating calcium level	Keg1<tm1b(KOMP)Mbp>/Keg1<tm1b(KOMP)Mbp>	C57BL/6N-Keg1<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6262745	M	MP:0003131	increased erythrocyte cell number	Keg1<tm1b(KOMP)Mbp>/Keg1<tm1b(KOMP)Mbp>	C57BL/6N-Keg1<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6262746	M	MP:0000221	decreased leukocyte cell number	Kif13b<tm1b(EUCOMM)Wtsi>/Kif13b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Kif13b<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262747	M	MP:0001552	increased circulating triglyceride level	Kif18b<tm1a(EUCOMM)Wtsi>/Kif18b<+>	C57BL/6N-Kif18b<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262751	M	MP:0001552	increased circulating triglyceride level	Kif2c<tm1.1(KOMP)Vlcg>/Kif2c<+>	C57BL/6N-Kif2c<tm1.1(KOMP)Vlcg>/Rbrc	N	MGI:5576271
MGI:6262754	F	MP:0001491	unresponsive to tactile stimuli	Kif5a<tm1b(EUCOMM)Wtsi>/Kif5a<tm1b(EUCOMM)Wtsi>	C57BL/6N-Kif5a<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262755	F	MP:0011962	increased cornea thickness	Klf12<tm1b(EUCOMM)Wtsi>/Klf12<+>	C57BL/6N-Klf12<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262755	M	MP:0005419	decreased circulating serum albumin level	Klf12<tm1b(EUCOMM)Wtsi>/Klf12<+>	C57BL/6N-Klf12<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6262757	M	MP:0001925	male infertility	Klhl10<tm1b(KOMP)Wtsi>/Klhl10<tm1b(KOMP)Wtsi>	C57BL/6N-Klhl10<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262757	M	MP:0000266	abnormal heart morphology	Klhl10<tm1b(KOMP)Wtsi>/Klhl10<tm1b(KOMP)Wtsi>	C57BL/6N-Klhl10<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262757	M	MP:0000274	enlarged heart	Klhl10<tm1b(KOMP)Wtsi>/Klhl10<tm1b(KOMP)Wtsi>	C57BL/6N-Klhl10<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262760	M	MP:0005505	thrombocytosis	Klhl42<tm1b(EUCOMM)Hmgu>/Klhl42<tm1b(EUCOMM)Hmgu>	C57BL/6N-Klhl42<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6262760	M	MP:0003960	increased lean body mass	Klhl42<tm1b(EUCOMM)Hmgu>/Klhl42<tm1b(EUCOMM)Hmgu>	C57BL/6N-Klhl42<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6262760	M	MP:0010123	increased bone mineral content	Klhl42<tm1b(EUCOMM)Hmgu>/Klhl42<tm1b(EUCOMM)Hmgu>	C57BL/6N-Klhl42<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6262763	M	MP:0002135	abnormal kidney morphology	Klrb1<tm1b(EUCOMM)Wtsi>/Klrb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Klrb1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262763	F	MP:0009476	enlarged cecum	Klrb1<tm1b(EUCOMM)Wtsi>/Klrb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Klrb1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262763	M	MP:0008528	polycystic kidney	Klrb1<tm1b(EUCOMM)Wtsi>/Klrb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Klrb1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262763	M	MP:0010052	increased grip strength	Klrb1<tm1b(EUCOMM)Wtsi>/Klrb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Klrb1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262763	M	MP:0000598	abnormal liver morphology	Klrb1<tm1b(EUCOMM)Wtsi>/Klrb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Klrb1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262763	M	MP:0010574	dilated aorta	Klrb1<tm1b(EUCOMM)Wtsi>/Klrb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Klrb1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262763	M	MP:0008173	increased follicular B cell number	Klrb1<tm1b(EUCOMM)Wtsi>/Klrb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Klrb1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262763	M	MP:0000221	decreased leukocyte cell number	Klrb1<tm1b(EUCOMM)Wtsi>/Klrb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Klrb1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262763	M	MP:0002059	abnormal seminal vesicle morphology	Klrb1<tm1b(EUCOMM)Wtsi>/Klrb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Klrb1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262765	M	MP:0001925	male infertility	Kpna2<em1(IMPC)Mbp>/Kpna2<em1(IMPC)Mbp>	C57BL/6N-Kpna2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262765	F	MP:0001926	female infertility	Kpna2<em1(IMPC)Mbp>/Kpna2<em1(IMPC)Mbp>	C57BL/6N-Kpna2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262769	M	MP:0010053	decreased grip strength	Krt2<tm1b(KOMP)Wtsi>/Krt2<+>	C57BL/6N-Krt2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262769	M	MP:0001147	small testis	Krt2<tm1b(KOMP)Wtsi>/Krt2<+>	C57BL/6N-Krt2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262769	M	MP:0001146	abnormal testis morphology	Krt2<tm1b(KOMP)Wtsi>/Krt2<+>	C57BL/6N-Krt2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262769	F	MP:0002135	abnormal kidney morphology	Krt2<tm1b(KOMP)Wtsi>/Krt2<+>	C57BL/6N-Krt2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262770	M	MP:0001510	abnormal coat appearance	Krt31<tm1e(KOMP)Wtsi>/Krt31<tm1e(KOMP)Wtsi>	C57BL/6N-Krt31<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262771	M	MP:0001406	abnormal gait	Krt90<em1(IMPC)J>/Krt90<em1(IMPC)J>	C57BL/6NJ-Krt90<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262773	M	MP:0011239	abnormal skin coloration	Kyat1<tm1b(KOMP)Wtsi>/Kyat1<+>	C57BL/6N-Kyat1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262775	M	MP:0001417	decreased exploration in new environment	Kynu<em1(IMPC)J>/Kynu<em1(IMPC)J>	C57BL/6NJ-Kynu<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262776	M	MP:0001552	increased circulating triglyceride level	L3mbtl3<em2(IMPC)Tcp>/L3mbtl3<+>	C57BL/6NCrl-L3mbtl3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262776	M	MP:0002060	abnormal skin morphology	L3mbtl3<em2(IMPC)Tcp>/L3mbtl3<+>	C57BL/6NCrl-L3mbtl3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262777	M	MP:0000562	polydactyly	L3mbtl3<em2(IMPC)Tcp>/L3mbtl3<em2(IMPC)Tcp>	C57BL/6NCrl-L3mbtl3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262779	M	MP:0005179	decreased circulating cholesterol level	Lactb<tm1.1(KOMP)Mbp>/Lactb<tm1.1(KOMP)Mbp>	C57BL/6N-Lactb<tm1.1(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:6262779	M	MP:0005344	increased circulating bilirubin level	Lactb<tm1.1(KOMP)Mbp>/Lactb<tm1.1(KOMP)Mbp>	C57BL/6N-Lactb<tm1.1(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:6262779	M	MP:0001289	persistence of hyaloid vascular system	Lactb<tm1.1(KOMP)Mbp>/Lactb<tm1.1(KOMP)Mbp>	C57BL/6N-Lactb<tm1.1(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:6262779	M	MP:0000274	enlarged heart	Lactb<tm1.1(KOMP)Mbp>/Lactb<tm1.1(KOMP)Mbp>	C57BL/6N-Lactb<tm1.1(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:6262779	M	MP:0000186	decreased circulating HDL cholesterol level	Lactb<tm1.1(KOMP)Mbp>/Lactb<tm1.1(KOMP)Mbp>	C57BL/6N-Lactb<tm1.1(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:6262779	M	MP:0010124	decreased bone mineral content	Lactb<tm1.1(KOMP)Mbp>/Lactb<tm1.1(KOMP)Mbp>	C57BL/6N-Lactb<tm1.1(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:6262784	M	MP:0005560	decreased circulating glucose level	Lcn2<tm1b(KOMP)Wtsi>/Lcn2<tm1b(KOMP)Wtsi>	C57BL/6N-Lcn2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262784	M	MP:0002833	increased heart weight	Lcn2<tm1b(KOMP)Wtsi>/Lcn2<tm1b(KOMP)Wtsi>	C57BL/6N-Lcn2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262784	M	MP:0004151	decreased circulating iron level	Lcn2<tm1b(KOMP)Wtsi>/Lcn2<tm1b(KOMP)Wtsi>	C57BL/6N-Lcn2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262784	M	MP:0005419	decreased circulating serum albumin level	Lcn2<tm1b(KOMP)Wtsi>/Lcn2<tm1b(KOMP)Wtsi>	C57BL/6N-Lcn2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262784	M	MP:0002590	increased mean corpuscular volume	Lcn2<tm1b(KOMP)Wtsi>/Lcn2<tm1b(KOMP)Wtsi>	C57BL/6N-Lcn2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262784	M	MP:0002959	increased urine microalbumin level	Lcn2<tm1b(KOMP)Wtsi>/Lcn2<tm1b(KOMP)Wtsi>	C57BL/6N-Lcn2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262785	M	MP:0000208	decreased hematocrit	Lcp1<tm1e.1(KOMP)Wtsi>/Lcp1<+>	C57BL/6N-Lcp1<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262785	M	MP:0013279	increased fasting circulating glucose level	Lcp1<tm1e.1(KOMP)Wtsi>/Lcp1<+>	C57BL/6N-Lcp1<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262785	F	MP:0002968	increased circulating alkaline phosphatase level	Lcp1<tm1e.1(KOMP)Wtsi>/Lcp1<+>	C57BL/6N-Lcp1<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262785	M	MP:0003179	thrombocytopenia	Lcp1<tm1e.1(KOMP)Wtsi>/Lcp1<+>	C57BL/6N-Lcp1<tm1e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262789	M	MP:0003068	enlarged kidney	Ldb3<tm2b(EUCOMM)Hmgu>/Ldb3<+>	C57BL/6N-Ldb3<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262789	M	MP:0001157	small seminal vesicle	Ldb3<tm2b(EUCOMM)Hmgu>/Ldb3<+>	C57BL/6N-Ldb3<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262789	M	MP:0001402	decreased locomotor activity	Ldb3<tm2b(EUCOMM)Hmgu>/Ldb3<+>	C57BL/6N-Ldb3<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262789	F	MP:0012362	increased large unstained cell number	Ldb3<tm2b(EUCOMM)Hmgu>/Ldb3<+>	C57BL/6N-Ldb3<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262789	F	MP:0010392	prolonged QRS complex duration	Ldb3<tm2b(EUCOMM)Hmgu>/Ldb3<+>	C57BL/6N-Ldb3<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262792	M	MP:0002590	increased mean corpuscular volume	Ldlr<tm1b(EUCOMM)Wtsi>/Ldlr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ldlr<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262792	M	MP:0010097	abnormal retina blood vessel morphology	Ldlr<tm1b(EUCOMM)Wtsi>/Ldlr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ldlr<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262793	M	MP:0000220	increased monocyte cell number	Lef1<tm1.1(KOMP)Vlcg>/Lef1<+>	C57BL/6N-Lef1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262793	F	MP:0000274	enlarged heart	Lef1<tm1.1(KOMP)Vlcg>/Lef1<+>	C57BL/6N-Lef1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262793	F	MP:0000266	abnormal heart morphology	Lef1<tm1.1(KOMP)Vlcg>/Lef1<+>	C57BL/6N-Lef1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262795	M	MP:0001406	abnormal gait	Lefty1<tm1b(KOMP)Wtsi>/Lefty1<+>	C57BL/6N-Lefty1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262795	M	MP:0010024	increased total body fat amount	Lefty1<tm1b(KOMP)Wtsi>/Lefty1<+>	C57BL/6N-Lefty1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262795	F	MP:0005627	increased circulating potassium level	Lefty1<tm1b(KOMP)Wtsi>/Lefty1<+>	C57BL/6N-Lefty1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262800	M	MP:0002079	increased circulating insulin level	Lipe<tm1b(KOMP)Wtsi>/Lipe<tm1b(KOMP)Wtsi>	C57BL/6N-Lipe<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262800	M	MP:0000274	enlarged heart	Lipe<tm1b(KOMP)Wtsi>/Lipe<tm1b(KOMP)Wtsi>	C57BL/6N-Lipe<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262800	M	MP:0001399	hyperactivity	Lipe<tm1b(KOMP)Wtsi>/Lipe<tm1b(KOMP)Wtsi>	C57BL/6N-Lipe<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262800	M	MP:0000266	abnormal heart morphology	Lipe<tm1b(KOMP)Wtsi>/Lipe<tm1b(KOMP)Wtsi>	C57BL/6N-Lipe<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262800	M	MP:0001925	male infertility	Lipe<tm1b(KOMP)Wtsi>/Lipe<tm1b(KOMP)Wtsi>	C57BL/6N-Lipe<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262800	M	MP:0003917	increased kidney weight	Lipe<tm1b(KOMP)Wtsi>/Lipe<tm1b(KOMP)Wtsi>	C57BL/6N-Lipe<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262802	M	MP:0001925	male infertility	Llcfc1<tm1.1(KOMP)Vlcg>/Llcfc1<tm1.1(KOMP)Vlcg>	C57BL/6N-Llcfc1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262802	M	MP:0005344	increased circulating bilirubin level	Llcfc1<tm1.1(KOMP)Vlcg>/Llcfc1<tm1.1(KOMP)Vlcg>	C57BL/6N-Llcfc1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262804	M	MP:0005559	increased circulating glucose level	Lmbrd1<tm1b(EUCOMM)Hmgu>/Lmbrd1<+>	C57BL/6N-Lmbrd1<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:6262806	M	MP:0000702	enlarged lymph nodes	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262806	M	MP:0000691	enlarged spleen	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262806	M	MP:0000538	abnormal urinary bladder morphology	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262806	M	MP:0002092	abnormal eye morphology	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262806	F	MP:0001258	decreased body length	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262806	M	MP:0000274	enlarged heart	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262806	M	MP:0000186	decreased circulating HDL cholesterol level	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262806	M	MP:0000219	increased neutrophil cell number	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262806	M	MP:0010025	decreased total body fat amount	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262806	M	MP:0001529	abnormal vocalization	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262806	M	MP:0005016	decreased lymphocyte cell number	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262806	M	MP:0011874	enlarged urinary bladder	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262806	M	MP:0003960	increased lean body mass	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262806	F	MP:0000709	enlarged thymus	Lmod3<em1(IMPC)Mbp>/Lmod3<em1(IMPC)Mbp>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262807	M	MP:0002059	abnormal seminal vesicle morphology	Lnpep<tm1b(KOMP)Wtsi>/Lnpep<tm1b(KOMP)Wtsi>	C57BL/6N-Lnpep<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262807	M	MP:0001363	increased anxiety-related response	Lnpep<tm1b(KOMP)Wtsi>/Lnpep<tm1b(KOMP)Wtsi>	C57BL/6N-Lnpep<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262810	M	MP:0002792	abnormal retina vasculature morphology	Lpcat1<tm1b(EUCOMM)Hmgu>/Lpcat1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lpcat1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262810	M	MP:0001399	hyperactivity	Lpcat1<tm1b(EUCOMM)Hmgu>/Lpcat1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lpcat1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262810	F	MP:0002546	mydriasis	Lpcat1<tm1b(EUCOMM)Hmgu>/Lpcat1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lpcat1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262810	F	MP:0006243	impaired pupillary reflex	Lpcat1<tm1b(EUCOMM)Hmgu>/Lpcat1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lpcat1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262811	F	MP:0005544	cornea deposits	Lpcat2b<tm1b(KOMP)Mbp>/Lpcat2b<tm1b(KOMP)Mbp>	C57BL/6N-Lpcat2b<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6262812	M	MP:0010124	decreased bone mineral content	Lpgat1<em1(IMPC)J>/Lpgat1<+>	C57BL/6NJ-Lpgat1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262813	F	MP:0001363	increased anxiety-related response	Lpgat1<em1(IMPC)J>/Lpgat1<em1(IMPC)J>	C57BL/6NJ-Lpgat1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262813	F	MP:0002574	increased vertical activity	Lpgat1<em1(IMPC)J>/Lpgat1<em1(IMPC)J>	C57BL/6NJ-Lpgat1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262814	F	MP:0005553	increased circulating creatinine level	Lrba<em1(IMPC)Wtsi>/Lrba<em1(IMPC)Wtsi>	C57BL/6N-Lrba<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262814	F	MP:0002968	increased circulating alkaline phosphatase level	Lrba<em1(IMPC)Wtsi>/Lrba<em1(IMPC)Wtsi>	C57BL/6N-Lrba<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262814	M	MP:0000023	abnormal ear position	Lrba<em1(IMPC)Wtsi>/Lrba<em1(IMPC)Wtsi>	C57BL/6N-Lrba<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262814	M	MP:0005178	increased circulating cholesterol level	Lrba<em1(IMPC)Wtsi>/Lrba<em1(IMPC)Wtsi>	C57BL/6N-Lrba<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262814	M	MP:0001556	increased circulating HDL cholesterol level	Lrba<em1(IMPC)Wtsi>/Lrba<em1(IMPC)Wtsi>	C57BL/6N-Lrba<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262814	F	MP:0005565	increased blood urea nitrogen level	Lrba<em1(IMPC)Wtsi>/Lrba<em1(IMPC)Wtsi>	C57BL/6N-Lrba<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262815	M	MP:0001510	abnormal coat appearance	Irag2<tm1b(EUCOMM)Wtsi>/Irag2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Irag2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262817	M	MP:0000745	tremors	Lrr1<em1(IMPC)H>/Lrr1<+>	C57BL/6NTac-Lrr1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262819	M	MP:0011110	preweaning lethality, incomplete penetrance	Lrrc10<tm1.1(KOMP)Vlcg>/Lrrc10<tm1.1(KOMP)Vlcg>	C57BL/6N-Lrrc10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262821	M	MP:0000194	increased circulating calcium level	Lrrc3<tm1b(EUCOMM)Hmgu>/Lrrc3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lrrc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262821	F	MP:0010053	decreased grip strength	Lrrc3<tm1b(EUCOMM)Hmgu>/Lrrc3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lrrc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262821	F	MP:0005016	decreased lymphocyte cell number	Lrrc3<tm1b(EUCOMM)Hmgu>/Lrrc3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lrrc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262821	M	MP:0001399	hyperactivity	Lrrc3<tm1b(EUCOMM)Hmgu>/Lrrc3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lrrc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262822	M	MP:0002757	decreased vertical activity	Lrrc49<tm1b(EUCOMM)Wtsi>/Lrrc49<+>	C57BL/6N-Lrrc49<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6262824	F	MP:0002092	abnormal eye morphology	Lrrc8a<tm1.1(KOMP)Vlcg>/Lrrc8a<+>	C57BL/6N-Lrrc8a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262824	F	MP:0001175	abnormal lung morphology	Lrrc8a<tm1.1(KOMP)Vlcg>/Lrrc8a<+>	C57BL/6N-Lrrc8a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262824	F	MP:0004882	enlarged lung	Lrrc8a<tm1.1(KOMP)Vlcg>/Lrrc8a<+>	C57BL/6N-Lrrc8a<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262826	F	MP:0002968	increased circulating alkaline phosphatase level	Lrrc8d<tm1a(EUCOMM)Wtsi>/Lrrc8d<tm1a(EUCOMM)Wtsi>	C57BL/6N-Lrrc8d<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262829	M	MP:0002874	decreased hemoglobin content	Lsm14a<tm1b(KOMP)Wtsi>/Lsm14a<+>	C57BL/6N-Lsm14a<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262829	M	MP:0000208	decreased hematocrit	Lsm14a<tm1b(KOMP)Wtsi>/Lsm14a<+>	C57BL/6N-Lsm14a<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262829	M	MP:0002875	decreased erythrocyte cell number	Lsm14a<tm1b(KOMP)Wtsi>/Lsm14a<+>	C57BL/6N-Lsm14a<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262829	M	MP:0002606	increased basophil cell number	Lsm14a<tm1b(KOMP)Wtsi>/Lsm14a<+>	C57BL/6N-Lsm14a<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6262830	F	MP:0001926	female infertility	Lsm14b<tm1b(KOMP)Mbp>/Lsm14b<tm1b(KOMP)Mbp>	C57BL/6N-Lsm14b<tm1b(KOMP)Mbp>/Wtsi	N	MGI:5576271
MGI:6262831	M	MP:0002968	increased circulating alkaline phosphatase level	Lss<tm1b(KOMP)Wtsi>/Lss<+>	C57BL/6N-Lss<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6262833	M	MP:0000198	decreased circulating phosphate level	Ly6g6d<tm1b(EUCOMM)Hmgu>/Ly6g6d<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ly6g6d<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262833	F	MP:0002599	increased mean platelet volume	Ly6g6d<tm1b(EUCOMM)Hmgu>/Ly6g6d<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ly6g6d<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262833	M	MP:0005554	decreased circulating creatinine level	Ly6g6d<tm1b(EUCOMM)Hmgu>/Ly6g6d<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ly6g6d<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262833	M	MP:0005628	decreased circulating potassium level	Ly6g6d<tm1b(EUCOMM)Hmgu>/Ly6g6d<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ly6g6d<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262833	M	MP:0002834	decreased heart weight	Ly6g6d<tm1b(EUCOMM)Hmgu>/Ly6g6d<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ly6g6d<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262834	F	MP:0002644	decreased circulating triglyceride level	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262834	M	MP:0002875	decreased erythrocyte cell number	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262834	F	MP:0000455	abnormal maxilla morphology	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262834	M	MP:0005343	increased circulating aspartate transaminase level	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262834	F	MP:0000063	decreased bone mineral density	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262834	M	MP:0002874	decreased hemoglobin content	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262834	M	MP:0010067	increased red blood cell distribution width	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262834	M	MP:0000208	decreased hematocrit	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262834	M	MP:0005011	increased eosinophil cell number	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262834	M	MP:0000186	decreased circulating HDL cholesterol level	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262834	F	MP:0002599	increased mean platelet volume	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262834	M	MP:0001325	abnormal retina morphology	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262834	F	MP:0000706	small thymus	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262834	M	MP:0001406	abnormal gait	Lyn<tm1b(EUCOMM)Hmgu>/Lyn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lyn<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262835	F	MP:0010052	increased grip strength	Lyplal1<tm1b(KOMP)Wtsi>/Lyplal1<tm1b(KOMP)Wtsi>	C57BL/6N-Lyplal1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6262836	M	MP:0001925	male infertility	Cfap91<em1(IMPC)Mbp>/Cfap91<em1(IMPC)Mbp>	C57BL/6N-Cfap91<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262836	M	MP:0001146	abnormal testis morphology	Cfap91<em1(IMPC)Mbp>/Cfap91<em1(IMPC)Mbp>	C57BL/6N-Cfap91<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262836	F	MP:0002092	abnormal eye morphology	Cfap91<em1(IMPC)Mbp>/Cfap91<em1(IMPC)Mbp>	C57BL/6N-Cfap91<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262836	M	MP:0001147	small testis	Cfap91<em1(IMPC)Mbp>/Cfap91<em1(IMPC)Mbp>	C57BL/6N-Cfap91<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262840	F	MP:0001399	hyperactivity	Map7d1<em1(IMPC)J>/Map7d1<+>	C57BL/6NJ-Map7d1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262841	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Mapk15<tm1b(EUCOMM)Hmgu>/Mapk15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapk15<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262841	F	MP:0001399	hyperactivity	Mapk15<tm1b(EUCOMM)Hmgu>/Mapk15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapk15<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262841	M	MP:0013278	decreased fasting circulating glucose level	Mapk15<tm1b(EUCOMM)Hmgu>/Mapk15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapk15<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262841	M	MP:0001402	decreased locomotor activity	Mapk15<tm1b(EUCOMM)Hmgu>/Mapk15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapk15<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262841	M	MP:0002075	abnormal coat/hair pigmentation	Mapk15<tm1b(EUCOMM)Hmgu>/Mapk15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapk15<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262843	F	MP:0002968	increased circulating alkaline phosphatase level	Marco<tm2b(EUCOMM)Hmgu>/Marco<tm2b(EUCOMM)Hmgu>	C57BL/6N-Marco<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262843	M	MP:0001406	abnormal gait	Marco<tm2b(EUCOMM)Hmgu>/Marco<tm2b(EUCOMM)Hmgu>	C57BL/6N-Marco<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262844	M	MP:0010024	increased total body fat amount	Mars2<tm1.1(KOMP)Vlcg>/Mars2<+>	C57BL/6N-Mars2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262844	M	MP:0003961	decreased lean body mass	Mars2<tm1.1(KOMP)Vlcg>/Mars2<+>	C57BL/6N-Mars2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262844	F	MP:0013278	decreased fasting circulating glucose level	Mars2<tm1.1(KOMP)Vlcg>/Mars2<+>	C57BL/6N-Mars2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262846	F	MP:0001304	cataract	Mast3<tm1.1(KOMP)Wtsi>/Mast3<tm1.1(KOMP)Wtsi>	C57BL/6N-Mast3<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262846	F	MP:0002968	increased circulating alkaline phosphatase level	Mast3<tm1.1(KOMP)Wtsi>/Mast3<tm1.1(KOMP)Wtsi>	C57BL/6N-Mast3<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6262848	M	MP:0003036	vertebral transformation	Mbd1<em1(IMPC)Wtsi>/Mbd1<em1(IMPC)Wtsi>	C57BL/6N-Mbd1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262848	M	MP:0000162	lordosis	Mbd1<em1(IMPC)Wtsi>/Mbd1<em1(IMPC)Wtsi>	C57BL/6N-Mbd1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262848	F	MP:0001926	female infertility	Mbd1<em1(IMPC)Wtsi>/Mbd1<em1(IMPC)Wtsi>	C57BL/6N-Mbd1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262852	M	MP:0005562	decreased mean corpuscular hemoglobin	Mccc2<em1(IMPC)J>/Mccc2<+>	C57BL/6NJ-Mccc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262852	M	MP:0002591	decreased mean corpuscular volume	Mccc2<em1(IMPC)J>/Mccc2<+>	C57BL/6NJ-Mccc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262852	M	MP:0000063	decreased bone mineral density	Mccc2<em1(IMPC)J>/Mccc2<+>	C57BL/6NJ-Mccc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262852	M	MP:0003131	increased erythrocyte cell number	Mccc2<em1(IMPC)J>/Mccc2<+>	C57BL/6NJ-Mccc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262854	M	MP:0000218	increased leukocyte cell number	Mcidas<em2(IMPC)Tcp>/Mcidas<em2(IMPC)Tcp>	C57BL/6NCrl-Mcidas<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262854	M	MP:0001925	male infertility	Mcidas<em2(IMPC)Tcp>/Mcidas<em2(IMPC)Tcp>	C57BL/6NCrl-Mcidas<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262854	M	MP:0002574	increased vertical activity	Mcidas<em2(IMPC)Tcp>/Mcidas<em2(IMPC)Tcp>	C57BL/6NCrl-Mcidas<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262854	M	MP:0002941	increased circulating alanine transaminase level	Mcidas<em2(IMPC)Tcp>/Mcidas<em2(IMPC)Tcp>	C57BL/6NCrl-Mcidas<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262854	F	MP:0005568	increased circulating total protein level	Mcidas<em2(IMPC)Tcp>/Mcidas<em2(IMPC)Tcp>	C57BL/6NCrl-Mcidas<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262854	F	MP:0001926	female infertility	Mcidas<em2(IMPC)Tcp>/Mcidas<em2(IMPC)Tcp>	C57BL/6NCrl-Mcidas<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262854	F	MP:0000689	abnormal spleen morphology	Mcidas<em2(IMPC)Tcp>/Mcidas<em2(IMPC)Tcp>	C57BL/6NCrl-Mcidas<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262854	M	MP:0003961	decreased lean body mass	Mcidas<em2(IMPC)Tcp>/Mcidas<em2(IMPC)Tcp>	C57BL/6NCrl-Mcidas<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262854	M	MP:0001489	decreased startle reflex	Mcidas<em2(IMPC)Tcp>/Mcidas<em2(IMPC)Tcp>	C57BL/6NCrl-Mcidas<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262856	F	MP:0001297	microphthalmia	Mcts1<em1(IMPC)Mbp>/Mcts1<em1(IMPC)Mbp>	C57BL/6N-Mcts1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262856	F	MP:0002092	abnormal eye morphology	Mcts1<em1(IMPC)Mbp>/Mcts1<em1(IMPC)Mbp>	C57BL/6N-Mcts1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262856	F	MP:0001304	cataract	Mcts1<em1(IMPC)Mbp>/Mcts1<em1(IMPC)Mbp>	C57BL/6N-Mcts1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262858	M	MP:0002059	abnormal seminal vesicle morphology	Me2<tm1b(EUCOMM)Hmgu>/Me2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Me2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262860	M	MP:0002590	increased mean corpuscular volume	Med10<em1(IMPC)J>/Med10<+>	C57BL/6NJ-Med10<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262860	F	MP:0010124	decreased bone mineral content	Med10<em1(IMPC)J>/Med10<+>	C57BL/6NJ-Med10<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262860	M	MP:0002875	decreased erythrocyte cell number	Med10<em1(IMPC)J>/Med10<+>	C57BL/6NJ-Med10<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262860	M	MP:0002874	decreased hemoglobin content	Med10<em1(IMPC)J>/Med10<+>	C57BL/6NJ-Med10<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262860	F	MP:0000063	decreased bone mineral density	Med10<em1(IMPC)J>/Med10<+>	C57BL/6NJ-Med10<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262862	M	MP:0001697	abnormal embryo size	Med16<tm1b(KOMP)Wtsi>/Med16<+>	C57BL/6N-Med16<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262862	M	MP:0004258	abnormal placenta size	Med16<tm1b(KOMP)Wtsi>/Med16<+>	C57BL/6N-Med16<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262863	M	MP:0011100	preweaning lethality, complete penetrance	Med17<tm1b(EUCOMM)Hmgu>/Med17<tm1b(EUCOMM)Hmgu>	C57BL/6N-Med17<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262866	F	MP:0000443	abnormal snout morphology	Mef2b<tm2b(EUCOMM)Hmgu>/Mef2b<tm2b(EUCOMM)Hmgu>	C57BL/6N-Mef2b<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262868	F	MP:0010123	increased bone mineral content	Mep1a<tm1a(KOMP)Wtsi>/Mep1a<tm1a(KOMP)Wtsi>	C57BL/6N-Mep1a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262868	M	MP:0010025	decreased total body fat amount	Mep1a<tm1a(KOMP)Wtsi>/Mep1a<tm1a(KOMP)Wtsi>	C57BL/6N-Mep1a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262868	M	MP:0013278	decreased fasting circulating glucose level	Mep1a<tm1a(KOMP)Wtsi>/Mep1a<tm1a(KOMP)Wtsi>	C57BL/6N-Mep1a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262868	F	MP:0003795	abnormal bone structure	Mep1a<tm1a(KOMP)Wtsi>/Mep1a<tm1a(KOMP)Wtsi>	C57BL/6N-Mep1a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262869	M	MP:0000692	small spleen	Mettl14<em1(IMPC)Tcp>/Mettl14<+>	C57BL/6NCrl-Mettl14<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262869	F	MP:0000689	abnormal spleen morphology	Mettl14<em1(IMPC)Tcp>/Mettl14<+>	C57BL/6NCrl-Mettl14<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262869	F	MP:0001120	abnormal uterus morphology	Mettl14<em1(IMPC)Tcp>/Mettl14<+>	C57BL/6NCrl-Mettl14<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262871	M	MP:0001556	increased circulating HDL cholesterol level	Mettl22<tm1.1(KOMP)Vlcg>/Mettl22<tm1.1(KOMP)Vlcg>	C57BL/6N-Mettl22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262871	M	MP:0005178	increased circulating cholesterol level	Mettl22<tm1.1(KOMP)Vlcg>/Mettl22<tm1.1(KOMP)Vlcg>	C57BL/6N-Mettl22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262872	F	MP:0002135	abnormal kidney morphology	Mettl26<tm1.1(KOMP)Vlcg>/Mettl26<tm1.1(KOMP)Vlcg>	C57BL/6N-Mettl26<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262872	M	MP:0010024	increased total body fat amount	Mettl26<tm1.1(KOMP)Vlcg>/Mettl26<tm1.1(KOMP)Vlcg>	C57BL/6N-Mettl26<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262873	M	MP:0000702	enlarged lymph nodes	Mfap4<tm1b(NCOM)Mfgc>/Mfap4<tm1b(NCOM)Mfgc>	C57BL/6N-Mfap4<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:6262874	F	MP:0003961	decreased lean body mass	Mfn2<tm1b(EUCOMM)Wtsi>/Mfn2<+>	C57BL/6N-Mfn2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262874	M	MP:0001406	abnormal gait	Mfn2<tm1b(EUCOMM)Wtsi>/Mfn2<+>	C57BL/6N-Mfn2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262876	F	MP:0000221	decreased leukocyte cell number	Mfsd10<tm1.1(KOMP)Vlcg>/Mfsd10<tm1.1(KOMP)Vlcg>	C57BL/6N-Mfsd10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262878	F	MP:0002075	abnormal coat/hair pigmentation	Mgme1<em1(IMPC)J>/Mgme1<em1(IMPC)J>	C57BL/6NJ-Mgme1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262878	M	MP:0003960	increased lean body mass	Mgme1<em1(IMPC)J>/Mgme1<em1(IMPC)J>	C57BL/6NJ-Mgme1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262878	M	MP:0010123	increased bone mineral content	Mgme1<em1(IMPC)J>/Mgme1<em1(IMPC)J>	C57BL/6NJ-Mgme1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262878	M	MP:0005292	improved glucose tolerance	Mgme1<em1(IMPC)J>/Mgme1<em1(IMPC)J>	C57BL/6NJ-Mgme1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262878	M	MP:0010025	decreased total body fat amount	Mgme1<em1(IMPC)J>/Mgme1<em1(IMPC)J>	C57BL/6NJ-Mgme1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262878	F	MP:0005561	increased mean corpuscular hemoglobin	Mgme1<em1(IMPC)J>/Mgme1<em1(IMPC)J>	C57BL/6NJ-Mgme1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262880	M	MP:0000702	enlarged lymph nodes	Mical2<em1(IMPC)Tcp>/Mical2<em1(IMPC)Tcp>	C57BL/6NCrl-Mical2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262880	M	MP:0002060	abnormal skin morphology	Mical2<em1(IMPC)Tcp>/Mical2<em1(IMPC)Tcp>	C57BL/6NCrl-Mical2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262880	M	MP:0002059	abnormal seminal vesicle morphology	Mical2<em1(IMPC)Tcp>/Mical2<em1(IMPC)Tcp>	C57BL/6NCrl-Mical2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262880	M	MP:0011874	enlarged urinary bladder	Mical2<em1(IMPC)Tcp>/Mical2<em1(IMPC)Tcp>	C57BL/6NCrl-Mical2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262880	M	MP:0004357	long tibia	Mical2<em1(IMPC)Tcp>/Mical2<em1(IMPC)Tcp>	C57BL/6NCrl-Mical2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262880	F	MP:0002989	small kidney	Mical2<em1(IMPC)Tcp>/Mical2<em1(IMPC)Tcp>	C57BL/6NCrl-Mical2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262880	F	MP:0002188	small heart	Mical2<em1(IMPC)Tcp>/Mical2<em1(IMPC)Tcp>	C57BL/6NCrl-Mical2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262880	F	MP:0004906	enlarged uterus	Mical2<em1(IMPC)Tcp>/Mical2<em1(IMPC)Tcp>	C57BL/6NCrl-Mical2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262880	F	MP:0001126	abnormal ovary morphology	Mical2<em1(IMPC)Tcp>/Mical2<em1(IMPC)Tcp>	C57BL/6NCrl-Mical2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262880	F	MP:0001297	microphthalmia	Mical2<em1(IMPC)Tcp>/Mical2<em1(IMPC)Tcp>	C57BL/6NCrl-Mical2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262880	M	MP:0003961	decreased lean body mass	Mical2<em1(IMPC)Tcp>/Mical2<em1(IMPC)Tcp>	C57BL/6NCrl-Mical2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262881	M	MP:0005419	decreased circulating serum albumin level	Micu2<tm1a(EUCOMM)Wtsi>/Micu2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Micu2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262881	M	MP:0010067	increased red blood cell distribution width	Micu2<tm1a(EUCOMM)Wtsi>/Micu2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Micu2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262881	M	MP:0010088	decreased circulating fructosamine level	Micu2<tm1a(EUCOMM)Wtsi>/Micu2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Micu2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262882	M	MP:0000691	enlarged spleen	Mid2<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Mid2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262882	M	MP:0000689	abnormal spleen morphology	Mid2<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Mid2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262882	M	MP:0002060	abnormal skin morphology	Mid2<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Mid2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262882	M	MP:0001192	scaly skin	Mid2<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Mid2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6262883	F	MP:0003731	abnormal retina outer nuclear layer morphology	Mif4gd<tm1b(KOMP)Wtsi>/Mif4gd<tm1b(KOMP)Wtsi>	C57BL/6N-Mif4gd<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6262884	F	MP:0020870	decreased thigmotaxis	Milr1<tm1b(EUCOMM)Hmgu>/Milr1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Milr1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262884	F	MP:0001399	hyperactivity	Milr1<tm1b(EUCOMM)Hmgu>/Milr1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Milr1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262884	M	MP:0010097	abnormal retina blood vessel morphology	Milr1<tm1b(EUCOMM)Hmgu>/Milr1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Milr1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262884	F	MP:0004924	abnormal behavior	Milr1<tm1b(EUCOMM)Hmgu>/Milr1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Milr1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262884	F	MP:0001364	decreased anxiety-related response	Milr1<tm1b(EUCOMM)Hmgu>/Milr1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Milr1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262885	F	MP:0000703	abnormal thymus morphology	Minar1<em1(IMPC)Tcp>/Minar1<em1(IMPC)Tcp>	C57BL/6NCrl-Minar1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262886	M	MP:0003961	decreased lean body mass	Mindy2<em1(IMPC)H>/Mindy2<em1(IMPC)H>	C57BL/6NTac-Mindy2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262886	M	MP:0005333	decreased heart rate	Mindy2<em1(IMPC)H>/Mindy2<em1(IMPC)H>	C57BL/6NTac-Mindy2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262886	M	MP:0010506	prolonged RR interval	Mindy2<em1(IMPC)H>/Mindy2<em1(IMPC)H>	C57BL/6NTac-Mindy2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262886	M	MP:0010024	increased total body fat amount	Mindy2<em1(IMPC)H>/Mindy2<em1(IMPC)H>	C57BL/6NTac-Mindy2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262886	M	MP:0010123	increased bone mineral content	Mindy2<em1(IMPC)H>/Mindy2<em1(IMPC)H>	C57BL/6NTac-Mindy2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262887	M	MP:0001392	abnormal locomotor behavior	Mindy4<em1(IMPC)H>/Mindy4<em1(IMPC)H>	C57BL/6NTac-Mindy4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262889	M	MP:0001925	male infertility	Mkrn2<em1(IMPC)Wtsi>/Mkrn2<em1(IMPC)Wtsi>	C57BL/6N-Mkrn2<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:6262892	F	MP:0001926	female infertility	Mlh3<tm1.1(KOMP)Vlcg>/Mlh3<tm1.1(KOMP)Vlcg>	C57BL/6N-Mlh3<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262892	M	MP:0001925	male infertility	Mlh3<tm1.1(KOMP)Vlcg>/Mlh3<tm1.1(KOMP)Vlcg>	C57BL/6N-Mlh3<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6262893	F	MP:0001417	decreased exploration in new environment	Mllt6<em1(IMPC)Tcp>/Mllt6<em1(IMPC)Tcp>	C57BL/6NCrl-Mllt6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262893	F	MP:0000219	increased neutrophil cell number	Mllt6<em1(IMPC)Tcp>/Mllt6<em1(IMPC)Tcp>	C57BL/6NCrl-Mllt6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262893	F	MP:0002599	increased mean platelet volume	Mllt6<em1(IMPC)Tcp>/Mllt6<em1(IMPC)Tcp>	C57BL/6NCrl-Mllt6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262893	M	MP:0000598	abnormal liver morphology	Mllt6<em1(IMPC)Tcp>/Mllt6<em1(IMPC)Tcp>	C57BL/6NCrl-Mllt6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262893	M	MP:0002768	small adrenal glands	Mllt6<em1(IMPC)Tcp>/Mllt6<em1(IMPC)Tcp>	C57BL/6NCrl-Mllt6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262893	M	MP:0000063	decreased bone mineral density	Mllt6<em1(IMPC)Tcp>/Mllt6<em1(IMPC)Tcp>	C57BL/6NCrl-Mllt6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262893	F	MP:0000691	enlarged spleen	Mllt6<em1(IMPC)Tcp>/Mllt6<em1(IMPC)Tcp>	C57BL/6NCrl-Mllt6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262893	F	MP:0001120	abnormal uterus morphology	Mllt6<em1(IMPC)Tcp>/Mllt6<em1(IMPC)Tcp>	C57BL/6NCrl-Mllt6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262893	M	MP:0002060	abnormal skin morphology	Mllt6<em1(IMPC)Tcp>/Mllt6<em1(IMPC)Tcp>	C57BL/6NCrl-Mllt6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262893	F	MP:0004952	increased spleen weight	Mllt6<em1(IMPC)Tcp>/Mllt6<em1(IMPC)Tcp>	C57BL/6NCrl-Mllt6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262893	F	MP:0000470	abnormal stomach morphology	Mllt6<em1(IMPC)Tcp>/Mllt6<em1(IMPC)Tcp>	C57BL/6NCrl-Mllt6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262894	M	MP:0002591	decreased mean corpuscular volume	Mlx<tm1.1(KOMP)Vlcg>/Mlx<tm1.1(KOMP)Vlcg>	C57BL/6N-Mlx<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262894	F	MP:0003960	increased lean body mass	Mlx<tm1.1(KOMP)Vlcg>/Mlx<tm1.1(KOMP)Vlcg>	C57BL/6N-Mlx<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262894	F	MP:0005560	decreased circulating glucose level	Mlx<tm1.1(KOMP)Vlcg>/Mlx<tm1.1(KOMP)Vlcg>	C57BL/6N-Mlx<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262894	F	MP:0005633	increased circulating sodium level	Mlx<tm1.1(KOMP)Vlcg>/Mlx<tm1.1(KOMP)Vlcg>	C57BL/6N-Mlx<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262894	F	MP:0010025	decreased total body fat amount	Mlx<tm1.1(KOMP)Vlcg>/Mlx<tm1.1(KOMP)Vlcg>	C57BL/6N-Mlx<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262894	F	MP:0001759	increased urine glucose level	Mlx<tm1.1(KOMP)Vlcg>/Mlx<tm1.1(KOMP)Vlcg>	C57BL/6N-Mlx<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262894	M	MP:0005562	decreased mean corpuscular hemoglobin	Mlx<tm1.1(KOMP)Vlcg>/Mlx<tm1.1(KOMP)Vlcg>	C57BL/6N-Mlx<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262894	M	MP:0013279	increased fasting circulating glucose level	Mlx<tm1.1(KOMP)Vlcg>/Mlx<tm1.1(KOMP)Vlcg>	C57BL/6N-Mlx<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262894	M	MP:0001925	male infertility	Mlx<tm1.1(KOMP)Vlcg>/Mlx<tm1.1(KOMP)Vlcg>	C57BL/6N-Mlx<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262895	F	MP:0005505	thrombocytosis	Mmaa<em1(IMPC)J>/Mmaa<em1(IMPC)J>	C57BL/6NJ-Mmaa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262895	F	MP:0003961	decreased lean body mass	Mmaa<em1(IMPC)J>/Mmaa<em1(IMPC)J>	C57BL/6NJ-Mmaa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262895	F	MP:0001417	decreased exploration in new environment	Mmaa<em1(IMPC)J>/Mmaa<em1(IMPC)J>	C57BL/6NJ-Mmaa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262895	F	MP:0020870	decreased thigmotaxis	Mmaa<em1(IMPC)J>/Mmaa<em1(IMPC)J>	C57BL/6NJ-Mmaa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262895	M	MP:0005333	decreased heart rate	Mmaa<em1(IMPC)J>/Mmaa<em1(IMPC)J>	C57BL/6NJ-Mmaa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262895	F	MP:0003795	abnormal bone structure	Mmaa<em1(IMPC)J>/Mmaa<em1(IMPC)J>	C57BL/6NJ-Mmaa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262895	M	MP:0000195	decreased circulating calcium level	Mmaa<em1(IMPC)J>/Mmaa<em1(IMPC)J>	C57BL/6NJ-Mmaa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262895	M	MP:0005344	increased circulating bilirubin level	Mmaa<em1(IMPC)J>/Mmaa<em1(IMPC)J>	C57BL/6NJ-Mmaa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262895	F	MP:0002757	decreased vertical activity	Mmaa<em1(IMPC)J>/Mmaa<em1(IMPC)J>	C57BL/6NJ-Mmaa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262895	M	MP:0005567	decreased circulating total protein level	Mmaa<em1(IMPC)J>/Mmaa<em1(IMPC)J>	C57BL/6NJ-Mmaa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262895	M	MP:0010506	prolonged RR interval	Mmaa<em1(IMPC)J>/Mmaa<em1(IMPC)J>	C57BL/6NJ-Mmaa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262895	F	MP:0001926	female infertility	Mmaa<em1(IMPC)J>/Mmaa<em1(IMPC)J>	C57BL/6NJ-Mmaa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6262896	F	MP:0002606	increased basophil cell number	Mmgt2<tm1b(EUCOMM)Wtsi>/Mmgt2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Mmgt2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262896	F	MP:0002075	abnormal coat/hair pigmentation	Mmgt2<tm1b(EUCOMM)Wtsi>/Mmgt2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Mmgt2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262896	M	MP:0005016	decreased lymphocyte cell number	Mmgt2<tm1b(EUCOMM)Wtsi>/Mmgt2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Mmgt2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262897	M	MP:0000220	increased monocyte cell number	Mmp11<tm1b(EUCOMM)Hmgu>/Mmp11<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mmp11<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262897	F	MP:0011965	decreased total retina thickness	Mmp11<tm1b(EUCOMM)Hmgu>/Mmp11<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mmp11<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262897	M	MP:0005419	decreased circulating serum albumin level	Mmp11<tm1b(EUCOMM)Hmgu>/Mmp11<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mmp11<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262897	F	MP:0002111	abnormal tail morphology	Mmp11<tm1b(EUCOMM)Hmgu>/Mmp11<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mmp11<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6262900	M	MP:0000186	decreased circulating HDL cholesterol level	Morc2a<em1(IMPC)Wtsi>/Morc2a<+>	C57BL/6N-Morc2a<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:6262904	F	MP:0002833	increased heart weight	Mos<tm1.1(KOMP)Vlcg>/Mos<tm1.1(KOMP)Vlcg>	C57BL/6N-Mos<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262905	M	MP:0000443	abnormal snout morphology	Mplkip<tm1.1(KOMP)Vlcg>/Mplkip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mplkip<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262905	M	MP:0002833	increased heart weight	Mplkip<tm1.1(KOMP)Vlcg>/Mplkip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mplkip<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262905	M	MP:0000274	enlarged heart	Mplkip<tm1.1(KOMP)Vlcg>/Mplkip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mplkip<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262905	M	MP:0001146	abnormal testis morphology	Mplkip<tm1.1(KOMP)Vlcg>/Mplkip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mplkip<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262905	M	MP:0020870	decreased thigmotaxis	Mplkip<tm1.1(KOMP)Vlcg>/Mplkip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mplkip<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262905	M	MP:0001147	small testis	Mplkip<tm1.1(KOMP)Vlcg>/Mplkip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mplkip<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262905	M	MP:0002060	abnormal skin morphology	Mplkip<tm1.1(KOMP)Vlcg>/Mplkip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mplkip<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262905	M	MP:0000063	decreased bone mineral density	Mplkip<tm1.1(KOMP)Vlcg>/Mplkip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mplkip<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262905	M	MP:0004924	abnormal behavior	Mplkip<tm1.1(KOMP)Vlcg>/Mplkip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mplkip<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262905	M	MP:0002135	abnormal kidney morphology	Mplkip<tm1.1(KOMP)Vlcg>/Mplkip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mplkip<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262905	M	MP:0000266	abnormal heart morphology	Mplkip<tm1.1(KOMP)Vlcg>/Mplkip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mplkip<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262905	M	MP:0001944	abnormal pancreas morphology	Mplkip<tm1.1(KOMP)Vlcg>/Mplkip<tm1.1(KOMP)Vlcg>	C57BL/6N-Mplkip<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262907	F	MP:0000218	increased leukocyte cell number	Mpped2<em1(IMPC)J>/Mpped2<em1(IMPC)J>	C57BL/6NJ-Mpped2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262907	M	MP:0001488	increased startle reflex	Mpped2<em1(IMPC)J>/Mpped2<em1(IMPC)J>	C57BL/6NJ-Mpped2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262908	M	MP:0002833	increased heart weight	Mpv17<em1(IMPC)J>/Mpv17<em1(IMPC)J>	C57BL/6NJ-Mpv17<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262908	M	MP:0005562	decreased mean corpuscular hemoglobin	Mpv17<em1(IMPC)J>/Mpv17<em1(IMPC)J>	C57BL/6NJ-Mpv17<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262908	M	MP:0005565	increased blood urea nitrogen level	Mpv17<em1(IMPC)J>/Mpv17<em1(IMPC)J>	C57BL/6NJ-Mpv17<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262908	F	MP:0003179	thrombocytopenia	Mpv17<em1(IMPC)J>/Mpv17<em1(IMPC)J>	C57BL/6NJ-Mpv17<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262909	M	MP:0010024	increased total body fat amount	Mpv17l2<tm1.1(KOMP)Mbp>/Mpv17l2<tm1.1(KOMP)Mbp>	C57BL/6N-Mpv17l2<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262909	F	MP:0000689	abnormal spleen morphology	Mpv17l2<tm1.1(KOMP)Mbp>/Mpv17l2<tm1.1(KOMP)Mbp>	C57BL/6N-Mpv17l2<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262909	F	MP:0000691	enlarged spleen	Mpv17l2<tm1.1(KOMP)Mbp>/Mpv17l2<tm1.1(KOMP)Mbp>	C57BL/6N-Mpv17l2<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262909	M	MP:0003961	decreased lean body mass	Mpv17l2<tm1.1(KOMP)Mbp>/Mpv17l2<tm1.1(KOMP)Mbp>	C57BL/6N-Mpv17l2<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6262910	F	MP:0009142	decreased prepulse inhibition	Mpz<em1(IMPC)Tcp>/Mpz<em1(IMPC)Tcp>	C57BL/6NCrl-Mpz<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262910	M	MP:0002060	abnormal skin morphology	Mpz<em1(IMPC)Tcp>/Mpz<em1(IMPC)Tcp>	C57BL/6NCrl-Mpz<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262910	M	MP:0013278	decreased fasting circulating glucose level	Mpz<em1(IMPC)Tcp>/Mpz<em1(IMPC)Tcp>	C57BL/6NCrl-Mpz<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262910	F	MP:0002599	increased mean platelet volume	Mpz<em1(IMPC)Tcp>/Mpz<em1(IMPC)Tcp>	C57BL/6NCrl-Mpz<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262910	M	MP:0001175	abnormal lung morphology	Mpz<em1(IMPC)Tcp>/Mpz<em1(IMPC)Tcp>	C57BL/6NCrl-Mpz<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262911	F	MP:0004357	long tibia	Mpzl2<tm1b(EUCOMM)Hmgu>/Mpzl2<+>	C57BL/6N-Mpzl2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262911	M	MP:0010067	increased red blood cell distribution width	Mpzl2<tm1b(EUCOMM)Hmgu>/Mpzl2<+>	C57BL/6N-Mpzl2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262912	M	MP:0001406	abnormal gait	Mpzl2<tm1b(EUCOMM)Hmgu>/Mpzl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mpzl2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262912	F	MP:0002102	abnormal ear morphology	Mpzl2<tm1b(EUCOMM)Hmgu>/Mpzl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mpzl2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262912	M	MP:0010024	increased total body fat amount	Mpzl2<tm1b(EUCOMM)Hmgu>/Mpzl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mpzl2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262912	F	MP:0002075	abnormal coat/hair pigmentation	Mpzl2<tm1b(EUCOMM)Hmgu>/Mpzl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mpzl2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6262913	F	MP:0001510	abnormal coat appearance	Mroh4<tm1b(KOMP)Wtsi>/Mroh4<tm1b(KOMP)Wtsi>	C57BL/6N-Mroh4<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262914	M	MP:0001925	male infertility	Mroh9<tm1a(EUCOMM)Wtsi>/Mroh9<tm1a(EUCOMM)Wtsi>	C57BL/6N-Mroh9<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262916	F	MP:0001289	persistence of hyaloid vascular system	Mrpl18<tm1.1(KOMP)Vlcg>/Mrpl18<+>	C57BL/6N-Mrpl18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262919	M	MP:0010124	decreased bone mineral content	Mrpl23<em1(IMPC)H>/Mrpl23<em1(IMPC)H>	C57BL/6NTac-Mrpl23<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262919	F	MP:0010052	increased grip strength	Mrpl23<em1(IMPC)H>/Mrpl23<em1(IMPC)H>	C57BL/6NTac-Mrpl23<em1(IMPC)H>/H	N	MGI:5576271
MGI:6262922	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Mrpl3<em1(IMPC)J>/Mrpl3<+>	C57BL/6NJ-Mrpl3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262922	F	MP:0002968	increased circulating alkaline phosphatase level	Mrpl3<em1(IMPC)J>/Mrpl3<+>	C57BL/6NJ-Mrpl3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262927	M	MP:0000208	decreased hematocrit	Mrpl58<tm1b(EUCOMM)Hmgu>/Mrpl58<+>	C57BL/6N-Mrpl58<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262927	F	MP:0000063	decreased bone mineral density	Mrpl58<tm1b(EUCOMM)Hmgu>/Mrpl58<+>	C57BL/6N-Mrpl58<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262929	F	MP:0005554	decreased circulating creatinine level	Mrps18c<tm1.1(KOMP)Vlcg>/Mrps18c<+>	C57BL/6N-Mrps18c<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262929	F	MP:0002875	decreased erythrocyte cell number	Mrps18c<tm1.1(KOMP)Vlcg>/Mrps18c<+>	C57BL/6N-Mrps18c<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262929	F	MP:0002874	decreased hemoglobin content	Mrps18c<tm1.1(KOMP)Vlcg>/Mrps18c<+>	C57BL/6N-Mrps18c<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262929	F	MP:0000208	decreased hematocrit	Mrps18c<tm1.1(KOMP)Vlcg>/Mrps18c<+>	C57BL/6N-Mrps18c<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262932	M	MP:0000063	decreased bone mineral density	Mrps22<tm1.1(KOMP)Vlcg>/Mrps22<+>	C57BL/6N-Mrps22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262932	M	MP:0010024	increased total body fat amount	Mrps22<tm1.1(KOMP)Vlcg>/Mrps22<+>	C57BL/6N-Mrps22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262932	M	MP:0010124	decreased bone mineral content	Mrps22<tm1.1(KOMP)Vlcg>/Mrps22<+>	C57BL/6N-Mrps22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262932	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Mrps22<tm1.1(KOMP)Vlcg>/Mrps22<+>	C57BL/6N-Mrps22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262932	F	MP:0001399	hyperactivity	Mrps22<tm1.1(KOMP)Vlcg>/Mrps22<+>	C57BL/6N-Mrps22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262932	M	MP:0003961	decreased lean body mass	Mrps22<tm1.1(KOMP)Vlcg>/Mrps22<+>	C57BL/6N-Mrps22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262932	F	MP:0005554	decreased circulating creatinine level	Mrps22<tm1.1(KOMP)Vlcg>/Mrps22<+>	C57BL/6N-Mrps22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262932	M	MP:0000218	increased leukocyte cell number	Mrps22<tm1.1(KOMP)Vlcg>/Mrps22<+>	C57BL/6N-Mrps22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262934	F	MP:0002339	abnormal lymph node morphology	Ms4a12<em1(IMPC)Mbp>/Ms4a12<em1(IMPC)Mbp>	C57BL/6N-Ms4a12<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262934	F	MP:0000702	enlarged lymph nodes	Ms4a12<em1(IMPC)Mbp>/Ms4a12<em1(IMPC)Mbp>	C57BL/6N-Ms4a12<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262934	F	MP:0002941	increased circulating alanine transaminase level	Ms4a12<em1(IMPC)Mbp>/Ms4a12<em1(IMPC)Mbp>	C57BL/6N-Ms4a12<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262935	F	MP:0001303	abnormal lens morphology	Msh5<tm1b(EUCOMM)Wtsi>/Msh5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Msh5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262935	F	MP:0000218	increased leukocyte cell number	Msh5<tm1b(EUCOMM)Wtsi>/Msh5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Msh5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262935	F	MP:0000063	decreased bone mineral density	Msh5<tm1b(EUCOMM)Wtsi>/Msh5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Msh5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262937	M	MP:0011100	preweaning lethality, complete penetrance	Mthfd2<tm1b(EUCOMM)Wtsi>/Mthfd2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Mthfd2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6262938	M	MP:0001417	decreased exploration in new environment	Mtif3<tm1b(EUCOMM)Wtsi>/Mtif3<+>	C57BL/6N-Mtif3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262938	F	MP:0000198	decreased circulating phosphate level	Mtif3<tm1b(EUCOMM)Wtsi>/Mtif3<+>	C57BL/6N-Mtif3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262938	F	MP:0003019	increased circulating chloride level	Mtif3<tm1b(EUCOMM)Wtsi>/Mtif3<+>	C57BL/6N-Mtif3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6262940	M	MP:0002591	decreased mean corpuscular volume	Mtmr3<tm1b(EUCOMM)Hmgu>/Mtmr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mtmr3<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262940	M	MP:0005562	decreased mean corpuscular hemoglobin	Mtmr3<tm1b(EUCOMM)Hmgu>/Mtmr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mtmr3<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262940	F	MP:0009142	decreased prepulse inhibition	Mtmr3<tm1b(EUCOMM)Hmgu>/Mtmr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mtmr3<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262940	M	MP:0006243	impaired pupillary reflex	Mtmr3<tm1b(EUCOMM)Hmgu>/Mtmr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mtmr3<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262940	M	MP:0001488	increased startle reflex	Mtmr3<tm1b(EUCOMM)Hmgu>/Mtmr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mtmr3<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262940	F	MP:0005627	increased circulating potassium level	Mtmr3<tm1b(EUCOMM)Hmgu>/Mtmr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mtmr3<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262940	M	MP:0005293	impaired glucose tolerance	Mtmr3<tm1b(EUCOMM)Hmgu>/Mtmr3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mtmr3<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6262941	M	MP:0005292	improved glucose tolerance	Mtnr1b<tm1.1(KOMP)Vlcg>/Mtnr1b<tm1.1(KOMP)Vlcg>	C57BL/6N-Mtnr1b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262941	M	MP:0013279	increased fasting circulating glucose level	Mtnr1b<tm1.1(KOMP)Vlcg>/Mtnr1b<tm1.1(KOMP)Vlcg>	C57BL/6N-Mtnr1b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6262946	M	MP:0002574	increased vertical activity	Pwwp3a<em1(IMPC)Tcp>/Pwwp3a<em1(IMPC)Tcp>	C57BL/6NCrl-Pwwp3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262946	F	MP:0001399	hyperactivity	Pwwp3a<em1(IMPC)Tcp>/Pwwp3a<em1(IMPC)Tcp>	C57BL/6NCrl-Pwwp3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262946	M	MP:0005505	thrombocytosis	Pwwp3a<em1(IMPC)Tcp>/Pwwp3a<em1(IMPC)Tcp>	C57BL/6NCrl-Pwwp3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262946	M	MP:0005565	increased blood urea nitrogen level	Pwwp3a<em1(IMPC)Tcp>/Pwwp3a<em1(IMPC)Tcp>	C57BL/6NCrl-Pwwp3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262946	M	MP:0000706	small thymus	Pwwp3a<em1(IMPC)Tcp>/Pwwp3a<em1(IMPC)Tcp>	C57BL/6NCrl-Pwwp3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262947	F	MP:0009709	hydrometra	Mvk<em1(IMPC)Tcp>/Mvk<+>	C57BL/6NCrl-Mvk<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262947	M	MP:0001147	small testis	Mvk<em1(IMPC)Tcp>/Mvk<+>	C57BL/6NCrl-Mvk<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262947	M	MP:0001297	microphthalmia	Mvk<em1(IMPC)Tcp>/Mvk<+>	C57BL/6NCrl-Mvk<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262947	M	MP:0001157	small seminal vesicle	Mvk<em1(IMPC)Tcp>/Mvk<+>	C57BL/6NCrl-Mvk<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262947	M	MP:0004930	small epididymis	Mvk<em1(IMPC)Tcp>/Mvk<+>	C57BL/6NCrl-Mvk<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262950	M	MP:0010024	increased total body fat amount	Myl2<tm1b(EUCOMM)Hmgu>/Myl2<+>	C57BL/6N-Myl2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262952	M	MP:0010025	decreased total body fat amount	Myl3<em1(IMPC)Wtsi>/Myl3<+>	C57BL/6N-Myl3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262952	M	MP:0003960	increased lean body mass	Myl3<em1(IMPC)Wtsi>/Myl3<+>	C57BL/6N-Myl3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262955	F	MP:0000063	decreased bone mineral density	Myo1d<em1(IMPC)J>/Myo1d<em1(IMPC)J>	C57BL/6NJ-Myo1d<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262959	M	MP:0010087	increased circulating fructosamine level	Myt1l<tm1a(EUCOMM)Wtsi>/Myt1l<tm1a(EUCOMM)Wtsi>	C57BL/6N-Myt1l<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262960	F	MP:0001120	abnormal uterus morphology	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0002339	abnormal lymph node morphology	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0000274	enlarged heart	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0001297	microphthalmia	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0003960	increased lean body mass	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0002060	abnormal skin morphology	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0001126	abnormal ovary morphology	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0000691	enlarged spleen	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0003068	enlarged kidney	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0002282	abnormal trachea morphology	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0002968	increased circulating alkaline phosphatase level	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0000702	enlarged lymph nodes	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0000266	abnormal heart morphology	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0002075	abnormal coat/hair pigmentation	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0005635	decreased circulating bilirubin level	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0000689	abnormal spleen morphology	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0002092	abnormal eye morphology	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0005292	improved glucose tolerance	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0010025	decreased total body fat amount	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0010052	increased grip strength	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262960	F	MP:0002135	abnormal kidney morphology	Naa10<em1(IMPC)Mbp>/Naa10<em1(IMPC)Mbp>	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6262962	M	MP:0001289	persistence of hyaloid vascular system	Nadk2<em1(IMPC)J>/Nadk2<+>	C57BL/6NJ-Nadk2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262962	F	MP:0013278	decreased fasting circulating glucose level	Nadk2<em1(IMPC)J>/Nadk2<+>	C57BL/6NJ-Nadk2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262962	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Nadk2<em1(IMPC)J>/Nadk2<+>	C57BL/6NJ-Nadk2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262964	M	MP:0000689	abnormal spleen morphology	Nalcn<em1(IMPC)Mbp>/Nalcn<+>	C57BL/6N-Nalcn<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262964	M	MP:0002135	abnormal kidney morphology	Nalcn<em1(IMPC)Mbp>/Nalcn<+>	C57BL/6N-Nalcn<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262964	M	MP:0010067	increased red blood cell distribution width	Nalcn<em1(IMPC)Mbp>/Nalcn<+>	C57BL/6N-Nalcn<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262964	M	MP:0000691	enlarged spleen	Nalcn<em1(IMPC)Mbp>/Nalcn<+>	C57BL/6N-Nalcn<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262964	M	MP:0000219	increased neutrophil cell number	Nalcn<em1(IMPC)Mbp>/Nalcn<+>	C57BL/6N-Nalcn<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6262966	M	MP:0020870	decreased thigmotaxis	Nars2<em1(IMPC)J>/Nars2<+>	C57BL/6NJ-Nars2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262966	M	MP:0001402	decreased locomotor activity	Nars2<em1(IMPC)J>/Nars2<+>	C57BL/6NJ-Nars2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262966	F	MP:0002075	abnormal coat/hair pigmentation	Nars2<em1(IMPC)J>/Nars2<+>	C57BL/6NJ-Nars2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262966	M	MP:0001417	decreased exploration in new environment	Nars2<em1(IMPC)J>/Nars2<+>	C57BL/6NJ-Nars2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262968	M	MP:0002060	abnormal skin morphology	Nav2<em1(IMPC)Tcp>/Nav2<em1(IMPC)Tcp>	C57BL/6NCrl-Nav2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262968	F	MP:0001417	decreased exploration in new environment	Nav2<em1(IMPC)Tcp>/Nav2<em1(IMPC)Tcp>	C57BL/6NCrl-Nav2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262968	F	MP:0002989	small kidney	Nav2<em1(IMPC)Tcp>/Nav2<em1(IMPC)Tcp>	C57BL/6NCrl-Nav2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262968	M	MP:0000219	increased neutrophil cell number	Nav2<em1(IMPC)Tcp>/Nav2<em1(IMPC)Tcp>	C57BL/6NCrl-Nav2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262968	M	MP:0005343	increased circulating aspartate transaminase level	Nav2<em1(IMPC)Tcp>/Nav2<em1(IMPC)Tcp>	C57BL/6NCrl-Nav2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6262976	M	MP:0001363	increased anxiety-related response	Ncbp2<em1(IMPC)J>/Ncbp2<+>	C57BL/6NJ-Ncbp2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262979	M	MP:0004974	decreased regulatory T cell number	Ncf2<tm1a(EUCOMM)Wtsi>/Ncf2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ncf2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262979	M	MP:0012765	decreased alpha-beta T cell number	Ncf2<tm1a(EUCOMM)Wtsi>/Ncf2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ncf2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262979	F	MP:0002599	increased mean platelet volume	Ncf2<tm1a(EUCOMM)Wtsi>/Ncf2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ncf2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262979	M	MP:0010053	decreased grip strength	Ncf2<tm1a(EUCOMM)Wtsi>/Ncf2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ncf2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262979	M	MP:0005018	decreased T cell number	Ncf2<tm1a(EUCOMM)Wtsi>/Ncf2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ncf2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262979	F	MP:0008810	increased circulating iron level	Ncf2<tm1a(EUCOMM)Wtsi>/Ncf2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Ncf2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262980	M	MP:0000274	enlarged heart	Nck1<tm1b(EUCOMM)Wtsi>/Nck1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Nck1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6262980	M	MP:0002060	abnormal skin morphology	Nck1<tm1b(EUCOMM)Wtsi>/Nck1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Nck1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6262980	M	MP:0002941	increased circulating alanine transaminase level	Nck1<tm1b(EUCOMM)Wtsi>/Nck1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Nck1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6262980	F	MP:0002092	abnormal eye morphology	Nck1<tm1b(EUCOMM)Wtsi>/Nck1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Nck1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6262980	F	MP:0002968	increased circulating alkaline phosphatase level	Nck1<tm1b(EUCOMM)Wtsi>/Nck1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Nck1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6262980	M	MP:0005343	increased circulating aspartate transaminase level	Nck1<tm1b(EUCOMM)Wtsi>/Nck1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Nck1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6262980	M	MP:0000266	abnormal heart morphology	Nck1<tm1b(EUCOMM)Wtsi>/Nck1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Nck1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6262983	F	MP:0010506	prolonged RR interval	Ndrg1<tm2b(KOMP)Wtsi>/Ndrg1<tm2b(KOMP)Wtsi>	C57BL/6N-Ndrg1<tm2b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262983	F	MP:0000063	decreased bone mineral density	Ndrg1<tm2b(KOMP)Wtsi>/Ndrg1<tm2b(KOMP)Wtsi>	C57BL/6N-Ndrg1<tm2b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262983	M	MP:0013278	decreased fasting circulating glucose level	Ndrg1<tm2b(KOMP)Wtsi>/Ndrg1<tm2b(KOMP)Wtsi>	C57BL/6N-Ndrg1<tm2b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262983	M	MP:0000745	tremors	Ndrg1<tm2b(KOMP)Wtsi>/Ndrg1<tm2b(KOMP)Wtsi>	C57BL/6N-Ndrg1<tm2b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6262986	M	MP:0009142	decreased prepulse inhibition	Ndufb9<tm1b(EUCOMM)Hmgu>/Ndufb9<+>	C57BL/6N-Ndufb9<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262986	M	MP:0002135	abnormal kidney morphology	Ndufb9<tm1b(EUCOMM)Hmgu>/Ndufb9<+>	C57BL/6N-Ndufb9<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262986	F	MP:0002966	decreased circulating alkaline phosphatase level	Ndufb9<tm1b(EUCOMM)Hmgu>/Ndufb9<+>	C57BL/6N-Ndufb9<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6262992	F	MP:0000208	decreased hematocrit	Ndufv1<tm1.1(KOMP)Vlcg>/Ndufv1<+>	C57BL/6N-Ndufv1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262992	F	MP:0002874	decreased hemoglobin content	Ndufv1<tm1.1(KOMP)Vlcg>/Ndufv1<+>	C57BL/6N-Ndufv1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262992	F	MP:0002875	decreased erythrocyte cell number	Ndufv1<tm1.1(KOMP)Vlcg>/Ndufv1<+>	C57BL/6N-Ndufv1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6262994	F	MP:0002160	abnormal reproductive system morphology	Nebl<tm1b(EUCOMM)Wtsi>/Nebl<tm1b(EUCOMM)Wtsi>	C57BL/6N-Nebl<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6262995	F	MP:0010053	decreased grip strength	Nectin4<em1(IMPC)J>/Nectin4<+>	C57BL/6NJ-Nectin4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262995	M	MP:0001417	decreased exploration in new environment	Nectin4<em1(IMPC)J>/Nectin4<+>	C57BL/6NJ-Nectin4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6262997	F	MP:0010052	increased grip strength	Nedd4<tm2b(EUCOMM)Hmgu>/Nedd4<+>	C57BL/6N-Nedd4<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262997	M	MP:0004924	abnormal behavior	Nedd4<tm2b(EUCOMM)Hmgu>/Nedd4<+>	C57BL/6N-Nedd4<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262997	F	MP:0005554	decreased circulating creatinine level	Nedd4<tm2b(EUCOMM)Hmgu>/Nedd4<+>	C57BL/6N-Nedd4<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262997	M	MP:0020870	decreased thigmotaxis	Nedd4<tm2b(EUCOMM)Hmgu>/Nedd4<+>	C57BL/6N-Nedd4<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262997	M	MP:0001402	decreased locomotor activity	Nedd4<tm2b(EUCOMM)Hmgu>/Nedd4<+>	C57BL/6N-Nedd4<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6262997	M	MP:0005293	impaired glucose tolerance	Nedd4<tm2b(EUCOMM)Hmgu>/Nedd4<+>	C57BL/6N-Nedd4<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263000	F	MP:0000195	decreased circulating calcium level	Neil2<em1(IMPC)J>/Neil2<em1(IMPC)J>	C57BL/6NJ-Neil2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263000	F	MP:0002574	increased vertical activity	Neil2<em1(IMPC)J>/Neil2<em1(IMPC)J>	C57BL/6NJ-Neil2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263000	F	MP:0001399	hyperactivity	Neil2<em1(IMPC)J>/Neil2<em1(IMPC)J>	C57BL/6NJ-Neil2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263001	F	MP:0002135	abnormal kidney morphology	Nek2<em1(IMPC)Tcp>/Nek2<em1(IMPC)Tcp>	C57BL/6NCrl-Nek2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263001	M	MP:0000702	enlarged lymph nodes	Nek2<em1(IMPC)Tcp>/Nek2<em1(IMPC)Tcp>	C57BL/6NCrl-Nek2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263002	M	MP:0013279	increased fasting circulating glucose level	Nek2<tm1b(KOMP)Wtsi>/Nek2<tm1b(KOMP)Wtsi>	C57BL/6N-Nek2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263002	M	MP:0001392	abnormal locomotor behavior	Nek2<tm1b(KOMP)Wtsi>/Nek2<tm1b(KOMP)Wtsi>	C57BL/6N-Nek2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263002	F	MP:0002833	increased heart weight	Nek2<tm1b(KOMP)Wtsi>/Nek2<tm1b(KOMP)Wtsi>	C57BL/6N-Nek2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263003	M	MP:0002959	increased urine microalbumin level	Nek7<tm1b(EUCOMM)Hmgu>/Nek7<+>	C57BL/6N-Nek7<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263006	M	MP:0000208	decreased hematocrit	Nemp1<em1(IMPC)Mbp>/Nemp1<em1(IMPC)Mbp>	C57BL/6NCrl-Nemp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263006	M	MP:0001146	abnormal testis morphology	Nemp1<em1(IMPC)Mbp>/Nemp1<em1(IMPC)Mbp>	C57BL/6NCrl-Nemp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263006	F	MP:0001926	female infertility	Nemp1<em1(IMPC)Mbp>/Nemp1<em1(IMPC)Mbp>	C57BL/6NCrl-Nemp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263006	M	MP:0002874	decreased hemoglobin content	Nemp1<em1(IMPC)Mbp>/Nemp1<em1(IMPC)Mbp>	C57BL/6NCrl-Nemp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263006	F	MP:0002092	abnormal eye morphology	Nemp1<em1(IMPC)Mbp>/Nemp1<em1(IMPC)Mbp>	C57BL/6NCrl-Nemp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263006	M	MP:0001147	small testis	Nemp1<em1(IMPC)Mbp>/Nemp1<em1(IMPC)Mbp>	C57BL/6NCrl-Nemp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263006	M	MP:0001402	decreased locomotor activity	Nemp1<em1(IMPC)Mbp>/Nemp1<em1(IMPC)Mbp>	C57BL/6NCrl-Nemp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	M	MP:0003642	absent seminal vesicle	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	F	MP:0002989	small kidney	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	F	MP:0000692	small spleen	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	M	MP:0000221	decreased leukocyte cell number	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	F	MP:0009342	enlarged gallbladder	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	M	MP:0002834	decreased heart weight	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	F	MP:0002135	abnormal kidney morphology	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	F	MP:0005084	abnormal gallbladder morphology	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	F	MP:0002060	abnormal skin morphology	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	F	MP:0000691	enlarged spleen	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	F	MP:0000689	abnormal spleen morphology	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	F	MP:0002092	abnormal eye morphology	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	F	MP:0006203	eye hemorrhage	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263008	M	MP:0000598	abnormal liver morphology	Neurl4<em1(IMPC)Mbp>/Neurl4<em1(IMPC)Mbp>	C57BL/6NCrl-Neurl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263010	M	MP:0003019	increased circulating chloride level	Nfat5<tm1b(KOMP)Wtsi>/Nfat5<+>	C57BL/6N-Nfat5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263010	M	MP:0000208	decreased hematocrit	Nfat5<tm1b(KOMP)Wtsi>/Nfat5<+>	C57BL/6N-Nfat5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263010	M	MP:0005344	increased circulating bilirubin level	Nfat5<tm1b(KOMP)Wtsi>/Nfat5<+>	C57BL/6N-Nfat5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263010	M	MP:0005633	increased circulating sodium level	Nfat5<tm1b(KOMP)Wtsi>/Nfat5<+>	C57BL/6N-Nfat5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263011	F	MP:0009709	hydrometra	Ngdn<tm1b(EUCOMM)Wtsi>/Ngdn<+>	C57BL/6N-Ngdn<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263013	F	MP:0009142	decreased prepulse inhibition	Nhlh1<tm1b(KOMP)Wtsi>/Nhlh1<+>	C57BL/6N-Nhlh1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263013	M	MP:0000702	enlarged lymph nodes	Nhlh1<tm1b(KOMP)Wtsi>/Nhlh1<+>	C57BL/6N-Nhlh1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263015	M	MP:0005293	impaired glucose tolerance	Nhlh2<em1(IMPC)Mbp>/Nhlh2<em1(IMPC)Mbp>	C57BL/6N-Nhlh2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263015	F	MP:0001926	female infertility	Nhlh2<em1(IMPC)Mbp>/Nhlh2<em1(IMPC)Mbp>	C57BL/6N-Nhlh2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263015	F	MP:0010124	decreased bone mineral content	Nhlh2<em1(IMPC)Mbp>/Nhlh2<em1(IMPC)Mbp>	C57BL/6N-Nhlh2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263015	M	MP:0001925	male infertility	Nhlh2<em1(IMPC)Mbp>/Nhlh2<em1(IMPC)Mbp>	C57BL/6N-Nhlh2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263015	M	MP:0000538	abnormal urinary bladder morphology	Nhlh2<em1(IMPC)Mbp>/Nhlh2<em1(IMPC)Mbp>	C57BL/6N-Nhlh2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263015	F	MP:0003961	decreased lean body mass	Nhlh2<em1(IMPC)Mbp>/Nhlh2<em1(IMPC)Mbp>	C57BL/6N-Nhlh2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263015	F	MP:0001402	decreased locomotor activity	Nhlh2<em1(IMPC)Mbp>/Nhlh2<em1(IMPC)Mbp>	C57BL/6N-Nhlh2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263015	F	MP:0000063	decreased bone mineral density	Nhlh2<em1(IMPC)Mbp>/Nhlh2<em1(IMPC)Mbp>	C57BL/6N-Nhlh2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263016	M	MP:0001417	decreased exploration in new environment	Nhs<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Nhs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263016	M	MP:0001488	increased startle reflex	Nhs<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Nhs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263017	F	MP:0001488	increased startle reflex	Nhs<em1(IMPC)Tcp>/Nhs<em1(IMPC)Tcp>	C57BL/6NCrl-Nhs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263017	F	MP:0010393	shortened QRS complex duration	Nhs<em1(IMPC)Tcp>/Nhs<em1(IMPC)Tcp>	C57BL/6NCrl-Nhs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263020	M	MP:0001410	head bobbing	Nisch<tm1b(EUCOMM)Hmgu>/Nisch<+>	C57BL/6N-Nisch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263020	M	MP:0005293	impaired glucose tolerance	Nisch<tm1b(EUCOMM)Hmgu>/Nisch<+>	C57BL/6N-Nisch<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263021	F	MP:0005562	decreased mean corpuscular hemoglobin	Nkg7<tm1.1(KOMP)Vlcg>/Nkg7<tm1.1(KOMP)Vlcg>	C57BL/6N-Nkg7<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263021	M	MP:0005011	increased eosinophil cell number	Nkg7<tm1.1(KOMP)Vlcg>/Nkg7<tm1.1(KOMP)Vlcg>	C57BL/6N-Nkg7<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263024	M	MP:0001488	increased startle reflex	Nlk<tm2b(KOMP)Wtsi>/Nlk<+>	C57BL/6N-Nlk<tm2b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6263027	F	MP:0004906	enlarged uterus	Nme2<tm1.1(KOMP)Vlcg>/Nme2<tm1.1(KOMP)Vlcg>	C57BL/6N-Nme2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263027	M	MP:0003068	enlarged kidney	Nme2<tm1.1(KOMP)Vlcg>/Nme2<tm1.1(KOMP)Vlcg>	C57BL/6N-Nme2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263027	F	MP:0001120	abnormal uterus morphology	Nme2<tm1.1(KOMP)Vlcg>/Nme2<tm1.1(KOMP)Vlcg>	C57BL/6N-Nme2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263027	M	MP:0000470	abnormal stomach morphology	Nme2<tm1.1(KOMP)Vlcg>/Nme2<tm1.1(KOMP)Vlcg>	C57BL/6N-Nme2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263027	F	MP:0000598	abnormal liver morphology	Nme2<tm1.1(KOMP)Vlcg>/Nme2<tm1.1(KOMP)Vlcg>	C57BL/6N-Nme2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263027	M	MP:0002135	abnormal kidney morphology	Nme2<tm1.1(KOMP)Vlcg>/Nme2<tm1.1(KOMP)Vlcg>	C57BL/6N-Nme2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263029	M	MP:0001325	abnormal retina morphology	Nmt2<tm2b(EUCOMM)Hmgu>/Nmt2<+>	C57BL/6N-Nmt2<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263029	F	MP:0002968	increased circulating alkaline phosphatase level	Nmt2<tm2b(EUCOMM)Hmgu>/Nmt2<+>	C57BL/6N-Nmt2<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263030	F	MP:0002339	abnormal lymph node morphology	Nnat<em1(IMPC)Mbp>/Nnat<em1(IMPC)Mbp>	C57BL/6NCrl-Nnat<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263030	M	MP:0010124	decreased bone mineral content	Nnat<em1(IMPC)Mbp>/Nnat<em1(IMPC)Mbp>	C57BL/6NCrl-Nnat<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263030	M	MP:0000274	enlarged heart	Nnat<em1(IMPC)Mbp>/Nnat<em1(IMPC)Mbp>	C57BL/6NCrl-Nnat<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263030	F	MP:0000702	enlarged lymph nodes	Nnat<em1(IMPC)Mbp>/Nnat<em1(IMPC)Mbp>	C57BL/6NCrl-Nnat<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263031	M	MP:0001556	increased circulating HDL cholesterol level	Nodal<tm1b(EUCOMM)Wtsi>/Nodal<+>	C57BL/6N-Nodal<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263031	M	MP:0001552	increased circulating triglyceride level	Nodal<tm1b(EUCOMM)Wtsi>/Nodal<+>	C57BL/6N-Nodal<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263031	F	MP:0010052	increased grip strength	Nodal<tm1b(EUCOMM)Wtsi>/Nodal<+>	C57BL/6N-Nodal<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263031	M	MP:0001402	decreased locomotor activity	Nodal<tm1b(EUCOMM)Wtsi>/Nodal<+>	C57BL/6N-Nodal<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263031	M	MP:0005178	increased circulating cholesterol level	Nodal<tm1b(EUCOMM)Wtsi>/Nodal<+>	C57BL/6N-Nodal<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263031	F	MP:0012362	increased large unstained cell number	Nodal<tm1b(EUCOMM)Wtsi>/Nodal<+>	C57BL/6N-Nodal<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263033	M	MP:0001488	increased startle reflex	Nolc1<tm1b(EUCOMM)Wtsi>/Nolc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Nolc1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263036	M	MP:0000137	abnormal vertebrae morphology	Notch1<tm1b(EUCOMM)Hmgu>/Notch1<+>	C57BL/6N-Notch1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263036	M	MP:0010052	increased grip strength	Notch1<tm1b(EUCOMM)Hmgu>/Notch1<+>	C57BL/6N-Notch1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263036	M	MP:0001488	increased startle reflex	Notch1<tm1b(EUCOMM)Hmgu>/Notch1<+>	C57BL/6N-Notch1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263037	F	MP:0000692	small spleen	Notum<em1(IMPC)Tcp>/Notum<+>	C57BL/6NCrl-Notum<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263037	F	MP:0001127	small ovary	Notum<em1(IMPC)Tcp>/Notum<+>	C57BL/6NCrl-Notum<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263037	F	MP:0010053	decreased grip strength	Notum<em1(IMPC)Tcp>/Notum<+>	C57BL/6NCrl-Notum<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263037	F	MP:0002637	small uterus	Notum<em1(IMPC)Tcp>/Notum<+>	C57BL/6NCrl-Notum<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263037	F	MP:0001120	abnormal uterus morphology	Notum<em1(IMPC)Tcp>/Notum<+>	C57BL/6NCrl-Notum<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263038	M	MP:0002135	abnormal kidney morphology	Notum<em1(IMPC)Tcp>/Notum<em1(IMPC)Tcp>	C57BL/6NCrl-Notum<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263038	M	MP:0002152	abnormal brain morphology	Notum<em1(IMPC)Tcp>/Notum<em1(IMPC)Tcp>	C57BL/6NCrl-Notum<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263040	M	MP:0001399	hyperactivity	Npff<tm1.1(KOMP)Vlcg>/Npff<tm1.1(KOMP)Vlcg>	C57BL/6N-Npff<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263042	M	MP:0001566	increased circulating phosphate level	Npr3<tm1.1(KOMP)Vlcg>/Npr3<+>	C57BL/6N-Npr3<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6263042	M	MP:0000266	abnormal heart morphology	Npr3<tm1.1(KOMP)Vlcg>/Npr3<+>	C57BL/6N-Npr3<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6263042	M	MP:0000274	enlarged heart	Npr3<tm1.1(KOMP)Vlcg>/Npr3<+>	C57BL/6N-Npr3<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6263043	M	MP:0002160	abnormal reproductive system morphology	Nr0b1<em2(IMPC)Wtsi>/Y	C57BL/6N-Nr0b1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263043	M	MP:0000182	increased circulating LDL cholesterol level	Nr0b1<em2(IMPC)Wtsi>/Y	C57BL/6N-Nr0b1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263043	M	MP:0010123	increased bone mineral content	Nr0b1<em2(IMPC)Wtsi>/Y	C57BL/6N-Nr0b1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263043	M	MP:0002965	increased circulating serum albumin level	Nr0b1<em2(IMPC)Wtsi>/Y	C57BL/6N-Nr0b1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263043	M	MP:0005564	increased hemoglobin content	Nr0b1<em2(IMPC)Wtsi>/Y	C57BL/6N-Nr0b1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263043	M	MP:0002968	increased circulating alkaline phosphatase level	Nr0b1<em2(IMPC)Wtsi>/Y	C57BL/6N-Nr0b1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263043	M	MP:0008810	increased circulating iron level	Nr0b1<em2(IMPC)Wtsi>/Y	C57BL/6N-Nr0b1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263043	M	MP:0010092	increased circulating magnesium level	Nr0b1<em2(IMPC)Wtsi>/Y	C57BL/6N-Nr0b1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263044	F	MP:0002941	increased circulating alanine transaminase level	Nr1d2<em1(IMPC)Mbp>/Nr1d2<em1(IMPC)Mbp>	C57BL/6N-Nr1d2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263047	F	MP:0003795	abnormal bone structure	Nr2f6<em1(IMPC)H>/Nr2f6<em1(IMPC)H>	C57BL/6N-Nr2f6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263047	F	MP:0010124	decreased bone mineral content	Nr2f6<em1(IMPC)H>/Nr2f6<em1(IMPC)H>	C57BL/6N-Nr2f6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263048	M	MP:0001363	increased anxiety-related response	Nrap<em1(IMPC)J>/Nrap<em1(IMPC)J>	C57BL/6NJ-Nrap<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263049	M	MP:0002764	short tibia	Nras<tm1b(EUCOMM)Hmgu>/Nras<+>	C57BL/6N-Nras<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263049	M	MP:0001556	increased circulating HDL cholesterol level	Nras<tm1b(EUCOMM)Hmgu>/Nras<+>	C57BL/6N-Nras<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263052	F	MP:0000947	convulsive seizures	Nrcam<tm2e.1(KOMP)Wtsi>/Nrcam<tm2e.1(KOMP)Wtsi>	C57BL/6N-Nrcam<tm2e.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263054	M	MP:0000745	tremors	Nrxn2<em1(IMPC)H>/Nrxn2<em1(IMPC)H>	C57BL/6NTac-Nrxn2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263054	F	MP:0001512	trunk curl	Nrxn2<em1(IMPC)H>/Nrxn2<em1(IMPC)H>	C57BL/6NTac-Nrxn2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263054	M	MP:0005565	increased blood urea nitrogen level	Nrxn2<em1(IMPC)H>/Nrxn2<em1(IMPC)H>	C57BL/6NTac-Nrxn2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263054	M	MP:0000274	enlarged heart	Nrxn2<em1(IMPC)H>/Nrxn2<em1(IMPC)H>	C57BL/6NTac-Nrxn2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263054	M	MP:0005178	increased circulating cholesterol level	Nrxn2<em1(IMPC)H>/Nrxn2<em1(IMPC)H>	C57BL/6NTac-Nrxn2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263054	F	MP:0001402	decreased locomotor activity	Nrxn2<em1(IMPC)H>/Nrxn2<em1(IMPC)H>	C57BL/6NTac-Nrxn2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263054	M	MP:0005568	increased circulating total protein level	Nrxn2<em1(IMPC)H>/Nrxn2<em1(IMPC)H>	C57BL/6NTac-Nrxn2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263054	M	MP:0001552	increased circulating triglyceride level	Nrxn2<em1(IMPC)H>/Nrxn2<em1(IMPC)H>	C57BL/6NTac-Nrxn2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263055	M	MP:0002075	abnormal coat/hair pigmentation	Nt5dc1<em1(IMPC)J>/Nt5dc1<em1(IMPC)J>	C57BL/6NJ-Nt5dc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263055	F	MP:0005560	decreased circulating glucose level	Nt5dc1<em1(IMPC)J>/Nt5dc1<em1(IMPC)J>	C57BL/6NJ-Nt5dc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263055	M	MP:0001486	abnormal startle reflex	Nt5dc1<em1(IMPC)J>/Nt5dc1<em1(IMPC)J>	C57BL/6NJ-Nt5dc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263055	M	MP:0001289	persistence of hyaloid vascular system	Nt5dc1<em1(IMPC)J>/Nt5dc1<em1(IMPC)J>	C57BL/6NJ-Nt5dc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263055	F	MP:0001363	increased anxiety-related response	Nt5dc1<em1(IMPC)J>/Nt5dc1<em1(IMPC)J>	C57BL/6NJ-Nt5dc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263056	F	MP:0005553	increased circulating creatinine level	Nt5dc2<em1(IMPC)J>/Nt5dc2<em1(IMPC)J>	C57BL/6NJ-Nt5dc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263056	M	MP:0001513	limb grasping	Nt5dc2<em1(IMPC)J>/Nt5dc2<em1(IMPC)J>	C57BL/6NJ-Nt5dc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263056	F	MP:0005565	increased blood urea nitrogen level	Nt5dc2<em1(IMPC)J>/Nt5dc2<em1(IMPC)J>	C57BL/6NJ-Nt5dc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263056	F	MP:0002110	abnormal digit morphology	Nt5dc2<em1(IMPC)J>/Nt5dc2<em1(IMPC)J>	C57BL/6NJ-Nt5dc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263056	F	MP:0000572	abnormal autopod morphology	Nt5dc2<em1(IMPC)J>/Nt5dc2<em1(IMPC)J>	C57BL/6NJ-Nt5dc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263056	M	MP:0001523	impaired righting response	Nt5dc2<em1(IMPC)J>/Nt5dc2<em1(IMPC)J>	C57BL/6NJ-Nt5dc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263058	M	MP:0001289	persistence of hyaloid vascular system	Nucks1<tm1b(EUCOMM)Hmgu>/Nucks1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nucks1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263058	M	MP:0002135	abnormal kidney morphology	Nucks1<tm1b(EUCOMM)Hmgu>/Nucks1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nucks1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263058	M	MP:0000702	enlarged lymph nodes	Nucks1<tm1b(EUCOMM)Hmgu>/Nucks1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nucks1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263058	F	MP:0002092	abnormal eye morphology	Nucks1<tm1b(EUCOMM)Hmgu>/Nucks1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nucks1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263058	M	MP:0005179	decreased circulating cholesterol level	Nucks1<tm1b(EUCOMM)Hmgu>/Nucks1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nucks1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263058	M	MP:0004002	abnormal jejunum morphology	Nucks1<tm1b(EUCOMM)Hmgu>/Nucks1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nucks1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263058	M	MP:0000470	abnormal stomach morphology	Nucks1<tm1b(EUCOMM)Hmgu>/Nucks1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nucks1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263058	M	MP:0000186	decreased circulating HDL cholesterol level	Nucks1<tm1b(EUCOMM)Hmgu>/Nucks1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nucks1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263060	M	MP:0002574	increased vertical activity	Nup37<tm1.1(KOMP)Vlcg>/Nup37<tm1.1(KOMP)Vlcg>	C57BL/6N-Nup37<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263060	M	MP:0000572	abnormal autopod morphology	Nup37<tm1.1(KOMP)Vlcg>/Nup37<tm1.1(KOMP)Vlcg>	C57BL/6N-Nup37<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263062	M	MP:0001925	male infertility	Nutm1<tm1b(KOMP)Wtsi>/Nutm1<tm1b(KOMP)Wtsi>	C57BL/6N-Nutm1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263062	M	MP:0003960	increased lean body mass	Nutm1<tm1b(KOMP)Wtsi>/Nutm1<tm1b(KOMP)Wtsi>	C57BL/6N-Nutm1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263062	M	MP:0010067	increased red blood cell distribution width	Nutm1<tm1b(KOMP)Wtsi>/Nutm1<tm1b(KOMP)Wtsi>	C57BL/6N-Nutm1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263062	M	MP:0005561	increased mean corpuscular hemoglobin	Nutm1<tm1b(KOMP)Wtsi>/Nutm1<tm1b(KOMP)Wtsi>	C57BL/6N-Nutm1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263062	M	MP:0010025	decreased total body fat amount	Nutm1<tm1b(KOMP)Wtsi>/Nutm1<tm1b(KOMP)Wtsi>	C57BL/6N-Nutm1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263062	M	MP:0005419	decreased circulating serum albumin level	Nutm1<tm1b(KOMP)Wtsi>/Nutm1<tm1b(KOMP)Wtsi>	C57BL/6N-Nutm1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263063	M	MP:0001925	male infertility	Nutm2<tm2b(EUCOMM)Wtsi>/Nutm2<tm2b(EUCOMM)Wtsi>	C57BL/6N-Nutm2<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263064	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Nxn<em1(IMPC)J>/Nxn<+>	C57BL/6NJ-Nxn<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263064	M	MP:0005344	increased circulating bilirubin level	Nxn<em1(IMPC)J>/Nxn<+>	C57BL/6NJ-Nxn<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263066	F	MP:0020420	abnormal freezing behavior	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263066	F	MP:0001392	abnormal locomotor behavior	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263066	F	MP:0001402	decreased locomotor activity	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263066	F	MP:0002968	increased circulating alkaline phosphatase level	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263066	F	MP:0001417	decreased exploration in new environment	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263068	F	MP:0005567	decreased circulating total protein level	Oaz2<em1(IMPC)J>/Oaz2<em1(IMPC)J>	C57BL/6NJ-Oaz2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263068	F	MP:0002590	increased mean corpuscular volume	Oaz2<em1(IMPC)J>/Oaz2<em1(IMPC)J>	C57BL/6NJ-Oaz2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263068	F	MP:0000195	decreased circulating calcium level	Oaz2<em1(IMPC)J>/Oaz2<em1(IMPC)J>	C57BL/6NJ-Oaz2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263069	M	MP:0001925	male infertility	Odf4<tm1.1(KOMP)Vlcg>/Odf4<tm1.1(KOMP)Vlcg>	C57BL/6N-Odf4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263069	M	MP:0000538	abnormal urinary bladder morphology	Odf4<tm1.1(KOMP)Vlcg>/Odf4<tm1.1(KOMP)Vlcg>	C57BL/6N-Odf4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263069	M	MP:0000274	enlarged heart	Odf4<tm1.1(KOMP)Vlcg>/Odf4<tm1.1(KOMP)Vlcg>	C57BL/6N-Odf4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263070	F	MP:0010053	decreased grip strength	Ofcc1<em1(IMPC)J>/Ofcc1<em1(IMPC)J>	C57BL/6NJ-Ofcc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263070	M	MP:0003179	thrombocytopenia	Ofcc1<em1(IMPC)J>/Ofcc1<em1(IMPC)J>	C57BL/6NJ-Ofcc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263070	M	MP:0001566	increased circulating phosphate level	Ofcc1<em1(IMPC)J>/Ofcc1<em1(IMPC)J>	C57BL/6NJ-Ofcc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263070	M	MP:0000556	abnormal hindlimb morphology	Ofcc1<em1(IMPC)J>/Ofcc1<em1(IMPC)J>	C57BL/6NJ-Ofcc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263072	F	MP:0001126	abnormal ovary morphology	Or1e1c<em1(IMPC)Mbp>/Or1e1c<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e1c<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263072	F	MP:0000494	abnormal cecum morphology	Or1e1c<em1(IMPC)Mbp>/Or1e1c<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e1c<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263072	F	MP:0005635	decreased circulating bilirubin level	Or1e1c<em1(IMPC)Mbp>/Or1e1c<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e1c<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263072	F	MP:0000266	abnormal heart morphology	Or1e1c<em1(IMPC)Mbp>/Or1e1c<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e1c<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263072	M	MP:0000598	abnormal liver morphology	Or1e1c<em1(IMPC)Mbp>/Or1e1c<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e1c<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263072	F	MP:0005632	decreased circulating aspartate transaminase level	Or1e1c<em1(IMPC)Mbp>/Or1e1c<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e1c<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263072	F	MP:0000274	enlarged heart	Or1e1c<em1(IMPC)Mbp>/Or1e1c<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e1c<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263072	F	MP:0004832	enlarged ovary	Or1e1c<em1(IMPC)Mbp>/Or1e1c<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e1c<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263072	F	MP:0009476	enlarged cecum	Or1e1c<em1(IMPC)Mbp>/Or1e1c<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e1c<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263073	F	MP:0002092	abnormal eye morphology	Or1e32<em1(IMPC)Mbp>/Or1e32<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e32<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263073	F	MP:0005278	abnormal cholesterol homeostasis	Or1e32<em1(IMPC)Mbp>/Or1e32<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e32<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263073	F	MP:0002339	abnormal lymph node morphology	Or1e32<em1(IMPC)Mbp>/Or1e32<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e32<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263073	M	MP:0009476	enlarged cecum	Or1e32<em1(IMPC)Mbp>/Or1e32<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e32<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263073	M	MP:0000494	abnormal cecum morphology	Or1e32<em1(IMPC)Mbp>/Or1e32<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e32<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263073	F	MP:0000702	enlarged lymph nodes	Or1e32<em1(IMPC)Mbp>/Or1e32<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e32<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263073	F	MP:0000639	abnormal adrenal gland morphology	Or1e32<em1(IMPC)Mbp>/Or1e32<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e32<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263073	F	MP:0002060	abnormal skin morphology	Or1e32<em1(IMPC)Mbp>/Or1e32<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e32<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263073	F	MP:0001293	anophthalmia	Or1e32<em1(IMPC)Mbp>/Or1e32<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e32<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263076	F	MP:0001289	persistence of hyaloid vascular system	Orc6<em1(IMPC)J>/Orc6<+>	C57BL/6NJ-Orc6<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263076	M	MP:0006243	impaired pupillary reflex	Orc6<em1(IMPC)J>/Orc6<+>	C57BL/6NJ-Orc6<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263076	F	MP:0005554	decreased circulating creatinine level	Orc6<em1(IMPC)J>/Orc6<+>	C57BL/6NJ-Orc6<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263077	M	MP:0001304	cataract	Osbpl10<em1(IMPC)J>/Osbpl10<em1(IMPC)J>	C57BL/6NJ-Osbpl10<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263078	M	MP:0002644	decreased circulating triglyceride level	Osbpl11<tm1b(EUCOMM)Hmgu>/Osbpl11<+>	C57BL/6N-Osbpl11<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263078	M	MP:0010024	increased total body fat amount	Osbpl11<tm1b(EUCOMM)Hmgu>/Osbpl11<+>	C57BL/6N-Osbpl11<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263078	M	MP:0005292	improved glucose tolerance	Osbpl11<tm1b(EUCOMM)Hmgu>/Osbpl11<+>	C57BL/6N-Osbpl11<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263080	M	MP:0002059	abnormal seminal vesicle morphology	Oscp1<tm1b(EUCOMM)Hmgu>/Oscp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Oscp1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263082	M	MP:0020870	decreased thigmotaxis	Otogl<em1(IMPC)J>/Otogl<em1(IMPC)J>	C57BL/6NJ-Otogl<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263082	F	MP:0002060	abnormal skin morphology	Otogl<em1(IMPC)J>/Otogl<em1(IMPC)J>	C57BL/6NJ-Otogl<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263085	M	MP:0001925	male infertility	Ovch2<tm1b(KOMP)Mbp>/Ovch2<tm1b(KOMP)Mbp>	C57BL/6N-Ovch2<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263086	M	MP:0001417	decreased exploration in new environment	P2rx5<tm1b(EUCOMM)Hmgu>/P2rx5<+>	C57BL/6N-P2rx5<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263086	M	MP:0001406	abnormal gait	P2rx5<tm1b(EUCOMM)Hmgu>/P2rx5<+>	C57BL/6N-P2rx5<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263088	F	MP:0011110	preweaning lethality, incomplete penetrance	P2ry13<tm1.1(KOMP)Vlcg>/P2ry13<tm1.1(KOMP)Vlcg>	C57BL/6N-P2ry13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263088	M	MP:0000266	abnormal heart morphology	P2ry13<tm1.1(KOMP)Vlcg>/P2ry13<tm1.1(KOMP)Vlcg>	C57BL/6N-P2ry13<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263089	M	MP:0002590	increased mean corpuscular volume	P3h3<tm1.1(KOMP)Vlcg>/P3h3<tm1.1(KOMP)Vlcg>	C57BL/6N-P3h3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263089	F	MP:0000198	decreased circulating phosphate level	P3h3<tm1.1(KOMP)Vlcg>/P3h3<tm1.1(KOMP)Vlcg>	C57BL/6N-P3h3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263091	M	MP:0001925	male infertility	Pacrg<em1(IMPC)J>/Pacrg<em1(IMPC)J>	C57BL/6NJ-Pacrg<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263091	F	MP:0001556	increased circulating HDL cholesterol level	Pacrg<em1(IMPC)J>/Pacrg<em1(IMPC)J>	C57BL/6NJ-Pacrg<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263092	M	MP:0003961	decreased lean body mass	Padi3<tm1b(KOMP)Wtsi>/Padi3<tm1b(KOMP)Wtsi>	C57BL/6N-Padi3<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6263092	M	MP:0010024	increased total body fat amount	Padi3<tm1b(KOMP)Wtsi>/Padi3<tm1b(KOMP)Wtsi>	C57BL/6N-Padi3<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6263098	M	MP:0002875	decreased erythrocyte cell number	Pank3<tm1b(KOMP)Mbp>/Pank3<tm1b(KOMP)Mbp>	C57BL/6N-Pank3<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6263098	F	MP:0001402	decreased locomotor activity	Pank3<tm1b(KOMP)Mbp>/Pank3<tm1b(KOMP)Mbp>	C57BL/6N-Pank3<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6263098	M	MP:0000219	increased neutrophil cell number	Pank3<tm1b(KOMP)Mbp>/Pank3<tm1b(KOMP)Mbp>	C57BL/6N-Pank3<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6263098	M	MP:0005016	decreased lymphocyte cell number	Pank3<tm1b(KOMP)Mbp>/Pank3<tm1b(KOMP)Mbp>	C57BL/6N-Pank3<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6263099	F	MP:0005562	decreased mean corpuscular hemoglobin	Panx1<tm1b(KOMP)Wtsi>/Panx1<tm1b(KOMP)Wtsi>	C57BL/6N-Panx1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263099	F	MP:0005419	decreased circulating serum albumin level	Panx1<tm1b(KOMP)Wtsi>/Panx1<tm1b(KOMP)Wtsi>	C57BL/6N-Panx1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263100	M	MP:0003179	thrombocytopenia	Paox<tm1.1(KOMP)Wtsi>/Paox<tm1.1(KOMP)Wtsi>	C57BL/6N-Paox<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263100	M	MP:0001399	hyperactivity	Paox<tm1.1(KOMP)Wtsi>/Paox<tm1.1(KOMP)Wtsi>	C57BL/6N-Paox<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263100	F	MP:0010097	abnormal retina blood vessel morphology	Paox<tm1.1(KOMP)Wtsi>/Paox<tm1.1(KOMP)Wtsi>	C57BL/6N-Paox<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263100	F	MP:0002792	abnormal retina vasculature morphology	Paox<tm1.1(KOMP)Wtsi>/Paox<tm1.1(KOMP)Wtsi>	C57BL/6N-Paox<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263100	M	MP:0005343	increased circulating aspartate transaminase level	Paox<tm1.1(KOMP)Wtsi>/Paox<tm1.1(KOMP)Wtsi>	C57BL/6N-Paox<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263100	F	MP:0013278	decreased fasting circulating glucose level	Paox<tm1.1(KOMP)Wtsi>/Paox<tm1.1(KOMP)Wtsi>	C57BL/6N-Paox<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263100	M	MP:0003928	increased heart rate variability	Paox<tm1.1(KOMP)Wtsi>/Paox<tm1.1(KOMP)Wtsi>	C57BL/6N-Paox<tm1.1(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263101	M	MP:0001925	male infertility	Papolb<tm1.1(KOMP)Vlcg>/Papolb<tm1.1(KOMP)Vlcg>	C57BL/6N-Papolb<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6263101	F	MP:0001120	abnormal uterus morphology	Papolb<tm1.1(KOMP)Vlcg>/Papolb<tm1.1(KOMP)Vlcg>	C57BL/6N-Papolb<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6263101	F	MP:0004906	enlarged uterus	Papolb<tm1.1(KOMP)Vlcg>/Papolb<tm1.1(KOMP)Vlcg>	C57BL/6N-Papolb<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6263101	M	MP:0000538	abnormal urinary bladder morphology	Papolb<tm1.1(KOMP)Vlcg>/Papolb<tm1.1(KOMP)Vlcg>	C57BL/6N-Papolb<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6263102	F	MP:0000219	increased neutrophil cell number	Parp12<tm1.1(KOMP)Vlcg>/Parp12<tm1.1(KOMP)Vlcg>	C57BL/6N-Parp12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263102	F	MP:0002599	increased mean platelet volume	Parp12<tm1.1(KOMP)Vlcg>/Parp12<tm1.1(KOMP)Vlcg>	C57BL/6N-Parp12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263102	M	MP:0001146	abnormal testis morphology	Parp12<tm1.1(KOMP)Vlcg>/Parp12<tm1.1(KOMP)Vlcg>	C57BL/6N-Parp12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263102	M	MP:0001147	small testis	Parp12<tm1.1(KOMP)Vlcg>/Parp12<tm1.1(KOMP)Vlcg>	C57BL/6N-Parp12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263102	F	MP:0001926	female infertility	Parp12<tm1.1(KOMP)Vlcg>/Parp12<tm1.1(KOMP)Vlcg>	C57BL/6N-Parp12<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263103	F	MP:0013523	increased memory-marker CD4-positive NK T cell number	Pax5<tm1b(EUCOMM)Wtsi>/Pax5<+>	C57BL/6N-Pax5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263103	F	MP:0013520	increased CD4-positive NK T cell number	Pax5<tm1b(EUCOMM)Wtsi>/Pax5<+>	C57BL/6N-Pax5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263103	M	MP:0008806	increased circulating amylase level	Pax5<tm1b(EUCOMM)Wtsi>/Pax5<+>	C57BL/6N-Pax5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263103	M	MP:0000221	decreased leukocyte cell number	Pax5<tm1b(EUCOMM)Wtsi>/Pax5<+>	C57BL/6N-Pax5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263103	M	MP:0001552	increased circulating triglyceride level	Pax5<tm1b(EUCOMM)Wtsi>/Pax5<+>	C57BL/6N-Pax5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263103	F	MP:0005387	immune system phenotype	Pax5<tm1b(EUCOMM)Wtsi>/Pax5<+>	C57BL/6N-Pax5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263103	M	MP:0011886	increased circulating lipase level	Pax5<tm1b(EUCOMM)Wtsi>/Pax5<+>	C57BL/6N-Pax5<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263106	F	MP:0001120	abnormal uterus morphology	Pbld2<tm1.1(KOMP)Vlcg>/Pbld2<tm1.1(KOMP)Vlcg>	C57BL/6N-Pbld2<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6263106	F	MP:0004906	enlarged uterus	Pbld2<tm1.1(KOMP)Vlcg>/Pbld2<tm1.1(KOMP)Vlcg>	C57BL/6N-Pbld2<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6263107	M	MP:0002135	abnormal kidney morphology	Pbrm1<tm1b(EUCOMM)Wtsi>/Pbrm1<+>	C57BL/6N-Pbrm1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263107	M	MP:0009142	decreased prepulse inhibition	Pbrm1<tm1b(EUCOMM)Wtsi>/Pbrm1<+>	C57BL/6N-Pbrm1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263107	F	MP:0001406	abnormal gait	Pbrm1<tm1b(EUCOMM)Wtsi>/Pbrm1<+>	C57BL/6N-Pbrm1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263109	M	MP:0010123	increased bone mineral content	Pcdh15<em1(IMPC)Wtsi>/Pcdh15<em1(IMPC)Wtsi>	C57BL/6N-Pcdh15<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263110	M	MP:0005343	increased circulating aspartate transaminase level	Pcdh9<tm1.1(KOMP)Vlcg>/Pcdh9<+>	C57BL/6N-Pcdh9<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263112	F	MP:0010506	prolonged RR interval	Pcm1<em1(IMPC)Tcp>/Pcm1<em1(IMPC)Tcp>	C57BL/6NCrl-Pcm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263112	M	MP:0002075	abnormal coat/hair pigmentation	Pcm1<em1(IMPC)Tcp>/Pcm1<em1(IMPC)Tcp>	C57BL/6NCrl-Pcm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263112	M	MP:0000438	abnormal cranium morphology	Pcm1<em1(IMPC)Tcp>/Pcm1<em1(IMPC)Tcp>	C57BL/6NCrl-Pcm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263112	F	MP:0000692	small spleen	Pcm1<em1(IMPC)Tcp>/Pcm1<em1(IMPC)Tcp>	C57BL/6NCrl-Pcm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263112	F	MP:0002060	abnormal skin morphology	Pcm1<em1(IMPC)Tcp>/Pcm1<em1(IMPC)Tcp>	C57BL/6NCrl-Pcm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263112	M	MP:0003961	decreased lean body mass	Pcm1<em1(IMPC)Tcp>/Pcm1<em1(IMPC)Tcp>	C57BL/6NCrl-Pcm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263112	M	MP:0001891	hydrocephaly	Pcm1<em1(IMPC)Tcp>/Pcm1<em1(IMPC)Tcp>	C57BL/6NCrl-Pcm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263112	M	MP:0001925	male infertility	Pcm1<em1(IMPC)Tcp>/Pcm1<em1(IMPC)Tcp>	C57BL/6NCrl-Pcm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263112	M	MP:0001488	increased startle reflex	Pcm1<em1(IMPC)Tcp>/Pcm1<em1(IMPC)Tcp>	C57BL/6NCrl-Pcm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263113	F	MP:0001304	cataract	Pcnx2<em1(IMPC)J>/Pcnx2<em1(IMPC)J>	C57BL/6NJ-Pcnx2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263114	F	MP:0002968	increased circulating alkaline phosphatase level	Pcsk9<tm2b(EUCOMM)Hmgu>/Pcsk9<tm2b(EUCOMM)Hmgu>	C57BL/6N-Pcsk9<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263114	F	MP:0008806	increased circulating amylase level	Pcsk9<tm2b(EUCOMM)Hmgu>/Pcsk9<tm2b(EUCOMM)Hmgu>	C57BL/6N-Pcsk9<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263114	F	MP:0011886	increased circulating lipase level	Pcsk9<tm2b(EUCOMM)Hmgu>/Pcsk9<tm2b(EUCOMM)Hmgu>	C57BL/6N-Pcsk9<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263115	F	MP:0003928	increased heart rate variability	Pcyox1l<em1(IMPC)J>/Pcyox1l<em1(IMPC)J>	C57BL/6NJ-Pcyox1l<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263115	F	MP:0005385	cardiovascular system phenotype	Pcyox1l<em1(IMPC)J>/Pcyox1l<em1(IMPC)J>	C57BL/6NJ-Pcyox1l<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263115	M	MP:0010024	increased total body fat amount	Pcyox1l<em1(IMPC)J>/Pcyox1l<em1(IMPC)J>	C57BL/6NJ-Pcyox1l<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263115	M	MP:0003961	decreased lean body mass	Pcyox1l<em1(IMPC)J>/Pcyox1l<em1(IMPC)J>	C57BL/6NJ-Pcyox1l<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263115	M	MP:0001489	decreased startle reflex	Pcyox1l<em1(IMPC)J>/Pcyox1l<em1(IMPC)J>	C57BL/6NJ-Pcyox1l<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263115	M	MP:0002834	decreased heart weight	Pcyox1l<em1(IMPC)J>/Pcyox1l<em1(IMPC)J>	C57BL/6NJ-Pcyox1l<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263115	F	MP:0004122	abnormal sinus arrhythmia	Pcyox1l<em1(IMPC)J>/Pcyox1l<em1(IMPC)J>	C57BL/6NJ-Pcyox1l<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263116	M	MP:0008528	polycystic kidney	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0002188	small heart	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0002834	decreased heart weight	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0002997	enlarged seminal vesicle	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	F	MP:0001258	decreased body length	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0001297	microphthalmia	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0001200	thick skin	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	F	MP:0002175	decreased brain weight	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0001147	small testis	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	F	MP:0003883	enlarged stomach	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0002339	abnormal lymph node morphology	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0002060	abnormal skin morphology	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	F	MP:0000691	enlarged spleen	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0000266	abnormal heart morphology	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	F	MP:0005635	decreased circulating bilirubin level	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0001556	increased circulating HDL cholesterol level	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0010052	increased grip strength	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0002092	abnormal eye morphology	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0001146	abnormal testis morphology	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	F	MP:0000470	abnormal stomach morphology	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0002059	abnormal seminal vesicle morphology	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0001175	abnormal lung morphology	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0000702	enlarged lymph nodes	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	F	MP:0000689	abnormal spleen morphology	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	M	MP:0001891	hydrocephaly	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263116	F	MP:0005565	increased blood urea nitrogen level	Pdcd6ip<em1(IMPC)Mbp>/Pdcd6ip<em1(IMPC)Mbp>	C57BL/6NCrl-Pdcd6ip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263117	M	MP:0001406	abnormal gait	Pde1a<em1(IMPC)H>/Pde1a<em1(IMPC)H>	C57BL/6N-Pde1a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263117	M	MP:0003960	increased lean body mass	Pde1a<em1(IMPC)H>/Pde1a<em1(IMPC)H>	C57BL/6N-Pde1a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263117	M	MP:0010025	decreased total body fat amount	Pde1a<em1(IMPC)H>/Pde1a<em1(IMPC)H>	C57BL/6N-Pde1a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263118	F	MP:0001399	hyperactivity	Pde4c<tm1.1(KOMP)Wtsi>/Pde4c<tm1.1(KOMP)Wtsi>	C57BL/6N-Pde4c<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263119	F	MP:0011960	abnormal eye anterior chamber depth	Pde4dip<tm1b(KOMP)Wtsi>/Pde4dip<+>	C57BL/6N-Pde4dip<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263119	M	MP:0005564	increased hemoglobin content	Pde4dip<tm1b(KOMP)Wtsi>/Pde4dip<+>	C57BL/6N-Pde4dip<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263119	M	MP:0010123	increased bone mineral content	Pde4dip<tm1b(KOMP)Wtsi>/Pde4dip<+>	C57BL/6N-Pde4dip<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263119	F	MP:0011962	increased cornea thickness	Pde4dip<tm1b(KOMP)Wtsi>/Pde4dip<+>	C57BL/6N-Pde4dip<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263121	F	MP:0000367	abnormal coat/ hair morphology	Pde6a<em2(IMPC)Mbp>/Pde6a<em2(IMPC)Mbp>	C57BL/6N-Pde6a<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263122	F	MP:0005565	increased blood urea nitrogen level	Pde7b<em1(IMPC)Mbp>/Pde7b<em1(IMPC)Mbp>	C57BL/6NCrl-Pde7b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263123	F	MP:0002699	abnormal vitreous body morphology	Pdhx<tm1b(EUCOMM)Hmgu>/Pdhx<+>	C57BL/6N-Pdhx<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263123	F	MP:0011965	decreased total retina thickness	Pdhx<tm1b(EUCOMM)Hmgu>/Pdhx<+>	C57BL/6N-Pdhx<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263125	M	MP:0005343	increased circulating aspartate transaminase level	Pdia4<tm1b(EUCOMM)Wtsi>/Pdia4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pdia4<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263125	M	MP:0010090	increased circulating creatine kinase level	Pdia4<tm1b(EUCOMM)Wtsi>/Pdia4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pdia4<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263126	F	MP:0001406	abnormal gait	Pdia6<tm1b(EUCOMM)Hmgu>/Pdia6<+>	C57BL/6N-Pdia6<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263126	F	MP:0013519	decreased CD4-positive NK T cell number	Pdia6<tm1b(EUCOMM)Hmgu>/Pdia6<+>	C57BL/6N-Pdia6<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263126	F	MP:0000702	enlarged lymph nodes	Pdia6<tm1b(EUCOMM)Hmgu>/Pdia6<+>	C57BL/6N-Pdia6<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263126	F	MP:0005355	enlarged thyroid gland	Pdia6<tm1b(EUCOMM)Hmgu>/Pdia6<+>	C57BL/6N-Pdia6<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263128	M	MP:0000274	enlarged heart	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	M	MP:0000598	abnormal liver morphology	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	M	MP:0001510	abnormal coat appearance	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	M	MP:0000639	abnormal adrenal gland morphology	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	F	MP:0009709	hydrometra	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	M	MP:0004931	enlarged epididymis	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	M	MP:0000538	abnormal urinary bladder morphology	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	F	MP:0010067	increased red blood cell distribution width	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	M	MP:0000266	abnormal heart morphology	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	F	MP:0004952	increased spleen weight	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	F	MP:0001120	abnormal uterus morphology	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	M	MP:0002631	abnormal epididymis morphology	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	M	MP:0001200	thick skin	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	M	MP:0002875	decreased erythrocyte cell number	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	M	MP:0000208	decreased hematocrit	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	F	MP:0000367	abnormal coat/ hair morphology	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	F	MP:0001293	anophthalmia	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	F	MP:0002092	abnormal eye morphology	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263128	M	MP:0002060	abnormal skin morphology	Pdik1l<em1(IMPC)Mbp>/Pdik1l<em1(IMPC)Mbp>	C57BL/6NCrl-Pdik1l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263130	F	MP:0001926	female infertility	Pdp1<em1(IMPC)Mbp>/Pdp1<em1(IMPC)Mbp>	C57BL/6NCrl-Pdp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263130	M	MP:0001147	small testis	Pdp1<em1(IMPC)Mbp>/Pdp1<em1(IMPC)Mbp>	C57BL/6NCrl-Pdp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263130	M	MP:0010053	decreased grip strength	Pdp1<em1(IMPC)Mbp>/Pdp1<em1(IMPC)Mbp>	C57BL/6NCrl-Pdp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263130	M	MP:0000274	enlarged heart	Pdp1<em1(IMPC)Mbp>/Pdp1<em1(IMPC)Mbp>	C57BL/6NCrl-Pdp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263130	M	MP:0000266	abnormal heart morphology	Pdp1<em1(IMPC)Mbp>/Pdp1<em1(IMPC)Mbp>	C57BL/6NCrl-Pdp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263130	M	MP:0005292	improved glucose tolerance	Pdp1<em1(IMPC)Mbp>/Pdp1<em1(IMPC)Mbp>	C57BL/6NCrl-Pdp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263130	M	MP:0002590	increased mean corpuscular volume	Pdp1<em1(IMPC)Mbp>/Pdp1<em1(IMPC)Mbp>	C57BL/6NCrl-Pdp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263130	M	MP:0002833	increased heart weight	Pdp1<em1(IMPC)Mbp>/Pdp1<em1(IMPC)Mbp>	C57BL/6NCrl-Pdp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263130	M	MP:0001146	abnormal testis morphology	Pdp1<em1(IMPC)Mbp>/Pdp1<em1(IMPC)Mbp>	C57BL/6NCrl-Pdp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263131	F	MP:0005278	abnormal cholesterol homeostasis	Pdpr<tm1b(EUCOMM)Wtsi>/Pdpr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pdpr<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263131	F	MP:0005554	decreased circulating creatinine level	Pdpr<tm1b(EUCOMM)Wtsi>/Pdpr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pdpr<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263131	M	MP:0002608	increased hematocrit	Pdpr<tm1b(EUCOMM)Wtsi>/Pdpr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pdpr<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263131	F	MP:0001402	decreased locomotor activity	Pdpr<tm1b(EUCOMM)Wtsi>/Pdpr<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pdpr<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263133	M	MP:0000598	abnormal liver morphology	Pdss1<em1(IMPC)Mbp>/Pdss1<+>	C57BL/6NCrl-Pdss1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263133	F	MP:0001304	cataract	Pdss1<em1(IMPC)Mbp>/Pdss1<+>	C57BL/6NCrl-Pdss1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263133	F	MP:0000639	abnormal adrenal gland morphology	Pdss1<em1(IMPC)Mbp>/Pdss1<+>	C57BL/6NCrl-Pdss1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263133	F	MP:0004832	enlarged ovary	Pdss1<em1(IMPC)Mbp>/Pdss1<+>	C57BL/6NCrl-Pdss1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263133	F	MP:0001126	abnormal ovary morphology	Pdss1<em1(IMPC)Mbp>/Pdss1<+>	C57BL/6NCrl-Pdss1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263135	M	MP:0012362	increased large unstained cell number	Pdzd8<tm1b(EUCOMM)Wtsi>/Pdzd8<+>	C57BL/6N-Pdzd8<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263136	F	MP:0001566	increased circulating phosphate level	Pdzd8<tm1b(EUCOMM)Wtsi>/Pdzd8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pdzd8<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263136	F	MP:0008806	increased circulating amylase level	Pdzd8<tm1b(EUCOMM)Wtsi>/Pdzd8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pdzd8<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263136	M	MP:0002098	abnormal vibrissa morphology	Pdzd8<tm1b(EUCOMM)Wtsi>/Pdzd8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pdzd8<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263136	F	MP:0001552	increased circulating triglyceride level	Pdzd8<tm1b(EUCOMM)Wtsi>/Pdzd8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pdzd8<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263136	F	MP:0003960	increased lean body mass	Pdzd8<tm1b(EUCOMM)Wtsi>/Pdzd8<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pdzd8<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263137	F	MP:0001289	persistence of hyaloid vascular system	Pdzrn3<em1(IMPC)J>/Pdzrn3<+>	C57BL/6NJ-Pdzrn3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263139	F	MP:0000063	decreased bone mineral density	Pebp1<em1(IMPC)Tcp>/Pebp1<em1(IMPC)Tcp>	C57BL/6NCrl-Pebp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263139	F	MP:0001417	decreased exploration in new environment	Pebp1<em1(IMPC)Tcp>/Pebp1<em1(IMPC)Tcp>	C57BL/6NCrl-Pebp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263139	M	MP:0000598	abnormal liver morphology	Pebp1<em1(IMPC)Tcp>/Pebp1<em1(IMPC)Tcp>	C57BL/6NCrl-Pebp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263139	M	MP:0002059	abnormal seminal vesicle morphology	Pebp1<em1(IMPC)Tcp>/Pebp1<em1(IMPC)Tcp>	C57BL/6NCrl-Pebp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263139	F	MP:0000702	enlarged lymph nodes	Pebp1<em1(IMPC)Tcp>/Pebp1<em1(IMPC)Tcp>	C57BL/6NCrl-Pebp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263139	M	MP:0002060	abnormal skin morphology	Pebp1<em1(IMPC)Tcp>/Pebp1<em1(IMPC)Tcp>	C57BL/6NCrl-Pebp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263139	M	MP:0005084	abnormal gallbladder morphology	Pebp1<em1(IMPC)Tcp>/Pebp1<em1(IMPC)Tcp>	C57BL/6NCrl-Pebp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263139	M	MP:0000266	abnormal heart morphology	Pebp1<em1(IMPC)Tcp>/Pebp1<em1(IMPC)Tcp>	C57BL/6NCrl-Pebp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263139	M	MP:0005012	decreased eosinophil cell number	Pebp1<em1(IMPC)Tcp>/Pebp1<em1(IMPC)Tcp>	C57BL/6NCrl-Pebp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263139	M	MP:0002631	abnormal epididymis morphology	Pebp1<em1(IMPC)Tcp>/Pebp1<em1(IMPC)Tcp>	C57BL/6NCrl-Pebp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263139	F	MP:0002989	small kidney	Pebp1<em1(IMPC)Tcp>/Pebp1<em1(IMPC)Tcp>	C57BL/6NCrl-Pebp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263139	F	MP:0001126	abnormal ovary morphology	Pebp1<em1(IMPC)Tcp>/Pebp1<em1(IMPC)Tcp>	C57BL/6NCrl-Pebp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263139	M	MP:0000692	small spleen	Pebp1<em1(IMPC)Tcp>/Pebp1<em1(IMPC)Tcp>	C57BL/6NCrl-Pebp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263140	M	MP:0002631	abnormal epididymis morphology	Peli3<tm1b(KOMP)Mbp>/Peli3<tm1b(KOMP)Mbp>	C57BL/6N-Peli3<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6263140	M	MP:0004931	enlarged epididymis	Peli3<tm1b(KOMP)Mbp>/Peli3<tm1b(KOMP)Mbp>	C57BL/6N-Peli3<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6263141	M	MP:0005343	increased circulating aspartate transaminase level	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	F	MP:0002757	decreased vertical activity	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	F	MP:0001399	hyperactivity	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	M	MP:0000702	enlarged lymph nodes	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	F	MP:0004924	abnormal behavior	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	F	MP:0001363	increased anxiety-related response	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	M	MP:0004151	decreased circulating iron level	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	F	MP:0002691	small stomach	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	F	MP:0002797	increased thigmotaxis	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	F	MP:0001402	decreased locomotor activity	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	F	MP:0010124	decreased bone mineral content	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	M	MP:0008174	decreased follicular B cell number	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	M	MP:0005017	decreased B cell number	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	M	MP:0002591	decreased mean corpuscular volume	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	M	MP:0013691	decreased CD5-positive Ly6C-positive T cell number	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	M	MP:0008207	decreased B-2 B cell number	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263141	M	MP:0000186	decreased circulating HDL cholesterol level	Pepd<tm1b(KOMP)Wtsi>/Pepd<tm1b(KOMP)Wtsi>	C57BL/6N-Pepd<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263142	M	MP:0010088	decreased circulating fructosamine level	Pes1<tm1b(EUCOMM)Wtsi>/Pes1<+>	C57BL/6N-Pes1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263142	M	MP:0005419	decreased circulating serum albumin level	Pes1<tm1b(EUCOMM)Wtsi>/Pes1<+>	C57BL/6N-Pes1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263142	M	MP:0005567	decreased circulating total protein level	Pes1<tm1b(EUCOMM)Wtsi>/Pes1<+>	C57BL/6N-Pes1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263144	F	MP:0011239	abnormal skin coloration	Pfdn5<tm1b(EUCOMM)Wtsi>/Pfdn5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pfdn5<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263144	F	MP:0002111	abnormal tail morphology	Pfdn5<tm1b(EUCOMM)Wtsi>/Pfdn5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pfdn5<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263144	F	MP:0000428	abnormal craniofacial morphology	Pfdn5<tm1b(EUCOMM)Wtsi>/Pfdn5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pfdn5<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263144	F	MP:0001785	edema	Pfdn5<tm1b(EUCOMM)Wtsi>/Pfdn5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pfdn5<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263144	F	MP:0003984	embryonic growth retardation	Pfdn5<tm1b(EUCOMM)Wtsi>/Pfdn5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pfdn5<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263144	F	MP:0001697	abnormal embryo size	Pfdn5<tm1b(EUCOMM)Wtsi>/Pfdn5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pfdn5<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263145	M	MP:0000063	decreased bone mineral density	Pfkfb3<tm1b(EUCOMM)Wtsi>/Pfkfb3<+>	C57BL/6N-Pfkfb3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263145	F	MP:0003795	abnormal bone structure	Pfkfb3<tm1b(EUCOMM)Wtsi>/Pfkfb3<+>	C57BL/6N-Pfkfb3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263147	F	MP:0000266	abnormal heart morphology	Pgbd1<em1(IMPC)Tcp>/Pgbd1<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263147	M	MP:0002768	small adrenal glands	Pgbd1<em1(IMPC)Tcp>/Pgbd1<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263147	M	MP:0001147	small testis	Pgbd1<em1(IMPC)Tcp>/Pgbd1<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263147	M	MP:0011874	enlarged urinary bladder	Pgbd1<em1(IMPC)Tcp>/Pgbd1<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263147	F	MP:0002060	abnormal skin morphology	Pgbd1<em1(IMPC)Tcp>/Pgbd1<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263147	M	MP:0000702	enlarged lymph nodes	Pgbd1<em1(IMPC)Tcp>/Pgbd1<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263147	F	MP:0001293	anophthalmia	Pgbd1<em1(IMPC)Tcp>/Pgbd1<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263147	F	MP:0002135	abnormal kidney morphology	Pgbd1<em1(IMPC)Tcp>/Pgbd1<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263147	F	MP:0001120	abnormal uterus morphology	Pgbd1<em1(IMPC)Tcp>/Pgbd1<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263147	F	MP:0002637	small uterus	Pgbd1<em1(IMPC)Tcp>/Pgbd1<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263147	M	MP:0004958	enlarged prostate gland	Pgbd1<em1(IMPC)Tcp>/Pgbd1<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263147	F	MP:0001944	abnormal pancreas morphology	Pgbd1<em1(IMPC)Tcp>/Pgbd1<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263147	F	MP:0002339	abnormal lymph node morphology	Pgbd1<em1(IMPC)Tcp>/Pgbd1<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263148	M	MP:0003068	enlarged kidney	Pgbd5<em1(IMPC)Tcp>/Pgbd5<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263148	F	MP:0010052	increased grip strength	Pgbd5<em1(IMPC)Tcp>/Pgbd5<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263148	F	MP:0002941	increased circulating alanine transaminase level	Pgbd5<em1(IMPC)Tcp>/Pgbd5<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263148	F	MP:0001293	anophthalmia	Pgbd5<em1(IMPC)Tcp>/Pgbd5<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263148	M	MP:0005293	impaired glucose tolerance	Pgbd5<em1(IMPC)Tcp>/Pgbd5<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263148	M	MP:0010024	increased total body fat amount	Pgbd5<em1(IMPC)Tcp>/Pgbd5<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263148	M	MP:0009516	enlarged salivary gland	Pgbd5<em1(IMPC)Tcp>/Pgbd5<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263148	F	MP:0001399	hyperactivity	Pgbd5<em1(IMPC)Tcp>/Pgbd5<em1(IMPC)Tcp>	C57BL/6NCrl-Pgbd5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263149	M	MP:0002092	abnormal eye morphology	Phactr1<em1(IMPC)Mbp>/Phactr1<em1(IMPC)Mbp>	C57BL/6NCrl-Phactr1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263149	M	MP:0002997	enlarged seminal vesicle	Phactr1<em1(IMPC)Mbp>/Phactr1<em1(IMPC)Mbp>	C57BL/6NCrl-Phactr1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263149	M	MP:0002060	abnormal skin morphology	Phactr1<em1(IMPC)Mbp>/Phactr1<em1(IMPC)Mbp>	C57BL/6NCrl-Phactr1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263149	M	MP:0000702	enlarged lymph nodes	Phactr1<em1(IMPC)Mbp>/Phactr1<em1(IMPC)Mbp>	C57BL/6NCrl-Phactr1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263149	M	MP:0002339	abnormal lymph node morphology	Phactr1<em1(IMPC)Mbp>/Phactr1<em1(IMPC)Mbp>	C57BL/6NCrl-Phactr1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263149	M	MP:0000689	abnormal spleen morphology	Phactr1<em1(IMPC)Mbp>/Phactr1<em1(IMPC)Mbp>	C57BL/6NCrl-Phactr1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263149	M	MP:0002135	abnormal kidney morphology	Phactr1<em1(IMPC)Mbp>/Phactr1<em1(IMPC)Mbp>	C57BL/6NCrl-Phactr1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263149	M	MP:0002059	abnormal seminal vesicle morphology	Phactr1<em1(IMPC)Mbp>/Phactr1<em1(IMPC)Mbp>	C57BL/6NCrl-Phactr1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263149	M	MP:0000221	decreased leukocyte cell number	Phactr1<em1(IMPC)Mbp>/Phactr1<em1(IMPC)Mbp>	C57BL/6NCrl-Phactr1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263149	F	MP:0000367	abnormal coat/ hair morphology	Phactr1<em1(IMPC)Mbp>/Phactr1<em1(IMPC)Mbp>	C57BL/6NCrl-Phactr1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263150	M	MP:0004956	decreased thymus weight	Phc3<tm2b(KOMP)Wtsi>/Phc3<tm2b(KOMP)Wtsi>	C57BL/6N-Phc3<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263152	F	MP:0004738	abnormal auditory brainstem response	Phf6<tm1b(EUCOMM)Wtsi>/Phf6<+>	C57BL/6N-Phf6<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263153	M	MP:0001925	male infertility	Phf7<em1(IMPC)Wtsi>/Phf7<em1(IMPC)Wtsi>	C57BL/6N-Phf7<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263154	M	MP:0002875	decreased erythrocyte cell number	Phf8<em2(IMPC)Wtsi>/Y	C57BL/6N-Phf8<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263154	M	MP:0005561	increased mean corpuscular hemoglobin	Phf8<em2(IMPC)Wtsi>/Y	C57BL/6N-Phf8<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263155	F	MP:0001697	abnormal embryo size	Phip<em1(IMPC)Tcp>/Phip<em1(IMPC)Tcp>	C57BL/6NCrl-Phip<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263156	M	MP:0003961	decreased lean body mass	Phkb<em1(IMPC)J>/Phkb<+>	C57BL/6NJ-Phkb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263156	F	MP:0001303	abnormal lens morphology	Phkb<em1(IMPC)J>/Phkb<+>	C57BL/6NJ-Phkb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263156	M	MP:0010024	increased total body fat amount	Phkb<em1(IMPC)J>/Phkb<+>	C57BL/6NJ-Phkb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263156	M	MP:0001513	limb grasping	Phkb<em1(IMPC)J>/Phkb<+>	C57BL/6NJ-Phkb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263157	M	MP:0002968	increased circulating alkaline phosphatase level	Phkb<em1(IMPC)J>/Phkb<em1(IMPC)J>	C57BL/6NJ-Phkb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263157	M	MP:0005343	increased circulating aspartate transaminase level	Phkb<em1(IMPC)J>/Phkb<em1(IMPC)J>	C57BL/6NJ-Phkb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263157	M	MP:0002941	increased circulating alanine transaminase level	Phkb<em1(IMPC)J>/Phkb<em1(IMPC)J>	C57BL/6NJ-Phkb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263158	F	MP:0001120	abnormal uterus morphology	Phtf1<tm1b(KOMP)Wtsi>/Phtf1<tm1b(KOMP)Wtsi>	C57BL/6N-Phtf1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263158	M	MP:0001944	abnormal pancreas morphology	Phtf1<tm1b(KOMP)Wtsi>/Phtf1<tm1b(KOMP)Wtsi>	C57BL/6N-Phtf1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263158	F	MP:0009709	hydrometra	Phtf1<tm1b(KOMP)Wtsi>/Phtf1<tm1b(KOMP)Wtsi>	C57BL/6N-Phtf1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263160	M	MP:0000538	abnormal urinary bladder morphology	Piezo1<tm1b(KOMP)Wtsi>/Piezo1<+>	C57BL/6N-Piezo1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263160	F	MP:0001402	decreased locomotor activity	Piezo1<tm1b(KOMP)Wtsi>/Piezo1<+>	C57BL/6N-Piezo1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263160	M	MP:0002941	increased circulating alanine transaminase level	Piezo1<tm1b(KOMP)Wtsi>/Piezo1<+>	C57BL/6N-Piezo1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263163	M	MP:0001722	pale yolk sac	Pigq<tm2b(EUCOMM)Wtsi>/Pigq<tm2b(EUCOMM)Wtsi>	C57BL/6N-Pigq<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263164	M	MP:0005016	decreased lymphocyte cell number	Pik3ap1<tm1b(KOMP)Wtsi>/Pik3ap1<tm1b(KOMP)Wtsi>	C57BL/6N-Pik3ap1<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6263164	F	MP:0005278	abnormal cholesterol homeostasis	Pik3ap1<tm1b(KOMP)Wtsi>/Pik3ap1<tm1b(KOMP)Wtsi>	C57BL/6N-Pik3ap1<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6263164	M	MP:0000219	increased neutrophil cell number	Pik3ap1<tm1b(KOMP)Wtsi>/Pik3ap1<tm1b(KOMP)Wtsi>	C57BL/6N-Pik3ap1<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6263164	M	MP:0000220	increased monocyte cell number	Pik3ap1<tm1b(KOMP)Wtsi>/Pik3ap1<tm1b(KOMP)Wtsi>	C57BL/6N-Pik3ap1<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6263165	M	MP:0013279	increased fasting circulating glucose level	Pip4k2c<tm1b(KOMP)Wtsi>/Pip4k2c<tm1b(KOMP)Wtsi>	C57BL/6N-Pip4k2c<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263166	M	MP:0010053	decreased grip strength	Pip5k1c<tm1b(KOMP)Wtsi>/Pip5k1c<+>	C57BL/6N-Pip5k1c<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263166	M	MP:0001289	persistence of hyaloid vascular system	Pip5k1c<tm1b(KOMP)Wtsi>/Pip5k1c<+>	C57BL/6N-Pip5k1c<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263166	F	MP:0002968	increased circulating alkaline phosphatase level	Pip5k1c<tm1b(KOMP)Wtsi>/Pip5k1c<+>	C57BL/6N-Pip5k1c<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263167	M	MP:0008730	fused phalanges	Pitx1<em1(IMPC)Wtsi>/Pitx1<+>	C57BL/6N-Pitx1<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6263167	M	MP:0000572	abnormal autopod morphology	Pitx1<em1(IMPC)Wtsi>/Pitx1<+>	C57BL/6N-Pitx1<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6263169	F	MP:0001304	cataract	Pja1<em1(IMPC)Mbp>/Pja1<em1(IMPC)Mbp>	C57BL/6NCrl-Pja1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263169	F	MP:0004832	enlarged ovary	Pja1<em1(IMPC)Mbp>/Pja1<em1(IMPC)Mbp>	C57BL/6NCrl-Pja1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263169	F	MP:0002092	abnormal eye morphology	Pja1<em1(IMPC)Mbp>/Pja1<em1(IMPC)Mbp>	C57BL/6NCrl-Pja1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263169	F	MP:0001126	abnormal ovary morphology	Pja1<em1(IMPC)Mbp>/Pja1<em1(IMPC)Mbp>	C57BL/6NCrl-Pja1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263169	F	MP:0001297	microphthalmia	Pja1<em1(IMPC)Mbp>/Pja1<em1(IMPC)Mbp>	C57BL/6NCrl-Pja1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263169	F	MP:0001402	decreased locomotor activity	Pja1<em1(IMPC)Mbp>/Pja1<em1(IMPC)Mbp>	C57BL/6NCrl-Pja1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263170	F	MP:0002966	decreased circulating alkaline phosphatase level	Pkd1<tm1b(EUCOMM)Hmgu>/Pkd1<+>	C57BL/6N-Pkd1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263170	F	MP:0002875	decreased erythrocyte cell number	Pkd1<tm1b(EUCOMM)Hmgu>/Pkd1<+>	C57BL/6N-Pkd1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263170	M	MP:0000219	increased neutrophil cell number	Pkd1<tm1b(EUCOMM)Hmgu>/Pkd1<+>	C57BL/6N-Pkd1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263173	F	MP:0001488	increased startle reflex	Pkig<tm1b(EUCOMM)Hmgu>/Pkig<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pkig<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263173	F	MP:0005565	increased blood urea nitrogen level	Pkig<tm1b(EUCOMM)Hmgu>/Pkig<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pkig<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263173	F	MP:0011965	decreased total retina thickness	Pkig<tm1b(EUCOMM)Hmgu>/Pkig<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pkig<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263173	M	MP:0002792	abnormal retina vasculature morphology	Pkig<tm1b(EUCOMM)Hmgu>/Pkig<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pkig<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263173	M	MP:0005343	increased circulating aspartate transaminase level	Pkig<tm1b(EUCOMM)Hmgu>/Pkig<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pkig<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263173	F	MP:0001319	irregularly shaped pupil	Pkig<tm1b(EUCOMM)Hmgu>/Pkig<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pkig<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263174	F	MP:0005567	decreased circulating total protein level	Pkn2<tm1b(KOMP)Wtsi>/Pkn2<+>	C57BL/6N-Pkn2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263174	F	MP:0005179	decreased circulating cholesterol level	Pkn2<tm1b(KOMP)Wtsi>/Pkn2<+>	C57BL/6N-Pkn2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263174	F	MP:0011897	decreased circulating unsaturated transferrin level	Pkn2<tm1b(KOMP)Wtsi>/Pkn2<+>	C57BL/6N-Pkn2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263174	F	MP:0000186	decreased circulating HDL cholesterol level	Pkn2<tm1b(KOMP)Wtsi>/Pkn2<+>	C57BL/6N-Pkn2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263174	F	MP:0005344	increased circulating bilirubin level	Pkn2<tm1b(KOMP)Wtsi>/Pkn2<+>	C57BL/6N-Pkn2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263174	M	MP:0001488	increased startle reflex	Pkn2<tm1b(KOMP)Wtsi>/Pkn2<+>	C57BL/6N-Pkn2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263176	F	MP:0005293	impaired glucose tolerance	Plaat3<em1(IMPC)Tcp>/Plaat3<em1(IMPC)Tcp>	C57BL/6NCrl-Plaat3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263176	F	MP:0000689	abnormal spleen morphology	Plaat3<em1(IMPC)Tcp>/Plaat3<em1(IMPC)Tcp>	C57BL/6NCrl-Plaat3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263176	M	MP:0005561	increased mean corpuscular hemoglobin	Plaat3<em1(IMPC)Tcp>/Plaat3<em1(IMPC)Tcp>	C57BL/6NCrl-Plaat3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263176	M	MP:0002833	increased heart weight	Plaat3<em1(IMPC)Tcp>/Plaat3<em1(IMPC)Tcp>	C57BL/6NCrl-Plaat3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263177	M	MP:0001925	male infertility	Pla2g2c<tm1b(EUCOMM)Wtsi>/Pla2g2c<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pla2g2c<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263178	M	MP:0000274	enlarged heart	Pla2g4b<tm1b(EUCOMM)Wtsi>/Pla2g4b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pla2g4b<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263178	F	MP:0001102	small superior vagus ganglion	Pla2g4b<tm1b(EUCOMM)Wtsi>/Pla2g4b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pla2g4b<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263178	M	MP:0002833	increased heart weight	Pla2g4b<tm1b(EUCOMM)Wtsi>/Pla2g4b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pla2g4b<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263178	F	MP:0009709	hydrometra	Pla2g4b<tm1b(EUCOMM)Wtsi>/Pla2g4b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pla2g4b<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263178	M	MP:0000266	abnormal heart morphology	Pla2g4b<tm1b(EUCOMM)Wtsi>/Pla2g4b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pla2g4b<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263179	F	MP:0002968	increased circulating alkaline phosphatase level	Pla2g7<em1(IMPC)J>/Pla2g7<em1(IMPC)J>	C57BL/6NJ-Pla2g7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263179	M	MP:0005566	decreased blood urea nitrogen level	Pla2g7<em1(IMPC)J>/Pla2g7<em1(IMPC)J>	C57BL/6NJ-Pla2g7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263179	M	MP:0005344	increased circulating bilirubin level	Pla2g7<em1(IMPC)J>/Pla2g7<em1(IMPC)J>	C57BL/6NJ-Pla2g7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263180	M	MP:0001510	abnormal coat appearance	Plac8<tm1b(EUCOMM)Hmgu>/Plac8<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plac8<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263180	F	MP:0001289	persistence of hyaloid vascular system	Plac8<tm1b(EUCOMM)Hmgu>/Plac8<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plac8<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263180	M	MP:0001325	abnormal retina morphology	Plac8<tm1b(EUCOMM)Hmgu>/Plac8<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plac8<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263181	F	MP:0002574	increased vertical activity	Plcb4<tm1b(EUCOMM)Wtsi>/Plcb4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Plcb4<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263181	F	MP:0011110	preweaning lethality, incomplete penetrance	Plcb4<tm1b(EUCOMM)Wtsi>/Plcb4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Plcb4<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263181	M	MP:0003960	increased lean body mass	Plcb4<tm1b(EUCOMM)Wtsi>/Plcb4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Plcb4<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263181	F	MP:0009342	enlarged gallbladder	Plcb4<tm1b(EUCOMM)Wtsi>/Plcb4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Plcb4<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263181	F	MP:0001120	abnormal uterus morphology	Plcb4<tm1b(EUCOMM)Wtsi>/Plcb4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Plcb4<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263181	F	MP:0005084	abnormal gallbladder morphology	Plcb4<tm1b(EUCOMM)Wtsi>/Plcb4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Plcb4<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263181	M	MP:0010025	decreased total body fat amount	Plcb4<tm1b(EUCOMM)Wtsi>/Plcb4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Plcb4<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263181	F	MP:0009709	hydrometra	Plcb4<tm1b(EUCOMM)Wtsi>/Plcb4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Plcb4<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263181	M	MP:0001392	abnormal locomotor behavior	Plcb4<tm1b(EUCOMM)Wtsi>/Plcb4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Plcb4<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263182	M	MP:0008935	decreased mean platelet volume	Plcz1<em1(IMPC)H>/Plcz1<em1(IMPC)H>	C57BL/6N-Plcz1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263182	F	MP:0001406	abnormal gait	Plcz1<em1(IMPC)H>/Plcz1<em1(IMPC)H>	C57BL/6N-Plcz1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263182	F	MP:0004151	decreased circulating iron level	Plcz1<em1(IMPC)H>/Plcz1<em1(IMPC)H>	C57BL/6N-Plcz1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263184	M	MP:0002079	increased circulating insulin level	Plet1<em1(IMPC)Wtsi>/Plet1<em1(IMPC)Wtsi>	C57BL/6N-Plet1<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6263187	M	MP:0000274	enlarged heart	Pmch<tm1.1(KOMP)Vlcg>/Pmch<tm1.1(KOMP)Vlcg>	C57BL/6N-Pmch<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263187	M	MP:0000266	abnormal heart morphology	Pmch<tm1.1(KOMP)Vlcg>/Pmch<tm1.1(KOMP)Vlcg>	C57BL/6N-Pmch<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263187	M	MP:0002135	abnormal kidney morphology	Pmch<tm1.1(KOMP)Vlcg>/Pmch<tm1.1(KOMP)Vlcg>	C57BL/6N-Pmch<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263187	F	MP:0010123	increased bone mineral content	Pmch<tm1.1(KOMP)Vlcg>/Pmch<tm1.1(KOMP)Vlcg>	C57BL/6N-Pmch<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263188	M	MP:0010025	decreased total body fat amount	Pmel<tm1b(EUCOMM)Wtsi>/Pmel<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pmel<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263188	M	MP:0001488	increased startle reflex	Pmel<tm1b(EUCOMM)Wtsi>/Pmel<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pmel<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263190	F	MP:0000274	enlarged heart	Pms1<tm1.1(KOMP)Vlcg>/Pms1<tm1.1(KOMP)Vlcg>	C57BL/6N-Pms1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6263190	F	MP:0000266	abnormal heart morphology	Pms1<tm1.1(KOMP)Vlcg>/Pms1<tm1.1(KOMP)Vlcg>	C57BL/6N-Pms1<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6263191	F	MP:0010123	increased bone mineral content	Pnck<tm1b(KOMP)Wtsi>/Pnck<tm1b(KOMP)Wtsi>	C57BL/6N-Pnck<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263191	F	MP:0001399	hyperactivity	Pnck<tm1b(KOMP)Wtsi>/Pnck<tm1b(KOMP)Wtsi>	C57BL/6N-Pnck<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263192	M	MP:0001257	increased body length	Pnpla1<tm1b(KOMP)Wtsi>/Pnpla1<+>	C57BL/6N-Pnpla1<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263194	M	MP:0002959	increased urine microalbumin level	Poc1a<tm1.1(KOMP)Mbp>/Poc1a<+>	C57BL/6N-Poc1a<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263195	F	MP:0001926	female infertility	Poc1a<tm1.1(KOMP)Mbp>/Poc1a<tm1.1(KOMP)Mbp>	C57BL/6N-Poc1a<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263195	M	MP:0001925	male infertility	Poc1a<tm1.1(KOMP)Mbp>/Poc1a<tm1.1(KOMP)Mbp>	C57BL/6N-Poc1a<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263196	F	MP:0001126	abnormal ovary morphology	Poc5<em1(IMPC)Tcp>/Poc5<em1(IMPC)Tcp>	C57BL/6NCrl-Poc5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263196	F	MP:0011110	preweaning lethality, incomplete penetrance	Poc5<em1(IMPC)Tcp>/Poc5<em1(IMPC)Tcp>	C57BL/6NCrl-Poc5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263196	M	MP:0001147	small testis	Poc5<em1(IMPC)Tcp>/Poc5<em1(IMPC)Tcp>	C57BL/6NCrl-Poc5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263196	M	MP:0001417	decreased exploration in new environment	Poc5<em1(IMPC)Tcp>/Poc5<em1(IMPC)Tcp>	C57BL/6NCrl-Poc5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263197	F	MP:0001120	abnormal uterus morphology	Podxl2<tm1.1(KOMP)Vlcg>/Podxl2<tm1.1(KOMP)Vlcg>	C57BL/6N-Podxl2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263197	F	MP:0000219	increased neutrophil cell number	Podxl2<tm1.1(KOMP)Vlcg>/Podxl2<tm1.1(KOMP)Vlcg>	C57BL/6N-Podxl2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263197	F	MP:0009709	hydrometra	Podxl2<tm1.1(KOMP)Vlcg>/Podxl2<tm1.1(KOMP)Vlcg>	C57BL/6N-Podxl2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263197	F	MP:0000689	abnormal spleen morphology	Podxl2<tm1.1(KOMP)Vlcg>/Podxl2<tm1.1(KOMP)Vlcg>	C57BL/6N-Podxl2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263197	F	MP:0002135	abnormal kidney morphology	Podxl2<tm1.1(KOMP)Vlcg>/Podxl2<tm1.1(KOMP)Vlcg>	C57BL/6N-Podxl2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263197	F	MP:0000691	enlarged spleen	Podxl2<tm1.1(KOMP)Vlcg>/Podxl2<tm1.1(KOMP)Vlcg>	C57BL/6N-Podxl2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263198	M	MP:0001325	abnormal retina morphology	Podxl<em1(IMPC)H>/Podxl<+>	C57BL/6N-Podxl<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263205	M	MP:0000702	enlarged lymph nodes	Polr3a<em2(IMPC)Tcp>/Polr3a<+>	C57BL/6NCrl-Polr3a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263205	M	MP:0010123	increased bone mineral content	Polr3a<em2(IMPC)Tcp>/Polr3a<+>	C57BL/6NCrl-Polr3a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263205	M	MP:0011874	enlarged urinary bladder	Polr3a<em2(IMPC)Tcp>/Polr3a<+>	C57BL/6NCrl-Polr3a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263205	M	MP:0002599	increased mean platelet volume	Polr3a<em2(IMPC)Tcp>/Polr3a<+>	C57BL/6NCrl-Polr3a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263210	M	MP:0004953	decreased spleen weight	Pou2af1<tm1b(KOMP)Wtsi>/Pou2af1<tm1b(KOMP)Wtsi>	C57BL/6N-Pou2af1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263211	M	MP:0002059	abnormal seminal vesicle morphology	Ppfibp2<em1(IMPC)Tcp>/Ppfibp2<em1(IMPC)Tcp>	C57BL/6NCrl-Ppfibp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263211	M	MP:0001200	thick skin	Ppfibp2<em1(IMPC)Tcp>/Ppfibp2<em1(IMPC)Tcp>	C57BL/6NCrl-Ppfibp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263211	M	MP:0000470	abnormal stomach morphology	Ppfibp2<em1(IMPC)Tcp>/Ppfibp2<em1(IMPC)Tcp>	C57BL/6NCrl-Ppfibp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263211	M	MP:0000702	enlarged lymph nodes	Ppfibp2<em1(IMPC)Tcp>/Ppfibp2<em1(IMPC)Tcp>	C57BL/6NCrl-Ppfibp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263211	M	MP:0011874	enlarged urinary bladder	Ppfibp2<em1(IMPC)Tcp>/Ppfibp2<em1(IMPC)Tcp>	C57BL/6NCrl-Ppfibp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263211	M	MP:0010053	decreased grip strength	Ppfibp2<em1(IMPC)Tcp>/Ppfibp2<em1(IMPC)Tcp>	C57BL/6NCrl-Ppfibp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263211	M	MP:0002060	abnormal skin morphology	Ppfibp2<em1(IMPC)Tcp>/Ppfibp2<em1(IMPC)Tcp>	C57BL/6NCrl-Ppfibp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263213	F	MP:0000702	enlarged lymph nodes	Ppl<tm1b(KOMP)Wtsi>/Ppl<tm1b(KOMP)Wtsi>	C57BL/6N-Ppl<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263213	M	MP:0002060	abnormal skin morphology	Ppl<tm1b(KOMP)Wtsi>/Ppl<tm1b(KOMP)Wtsi>	C57BL/6N-Ppl<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263213	M	MP:0002989	small kidney	Ppl<tm1b(KOMP)Wtsi>/Ppl<tm1b(KOMP)Wtsi>	C57BL/6N-Ppl<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263213	M	MP:0001417	decreased exploration in new environment	Ppl<tm1b(KOMP)Wtsi>/Ppl<tm1b(KOMP)Wtsi>	C57BL/6N-Ppl<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263214	M	MP:0012361	decreased large unstained cell number	Ppm1m<tm2b(EUCOMM)Hmgu>/Ppm1m<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ppm1m<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263215	M	MP:0001925	male infertility	Ppp1cc<em1(IMPC)Wtsi>/Ppp1cc<em1(IMPC)Wtsi>	C57BL/6N-Ppp1cc<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:6263215	M	MP:0005561	increased mean corpuscular hemoglobin	Ppp1cc<em1(IMPC)Wtsi>/Ppp1cc<em1(IMPC)Wtsi>	C57BL/6N-Ppp1cc<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:6263217	F	MP:0003795	abnormal bone structure	Ppp2r2a<tm1b(KOMP)Wtsi>/Ppp2r2a<+>	C57BL/6N-Ppp2r2a<tm1b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6263219	M	MP:0001925	male infertility	Ppp3cc<tm1b(EUCOMM)Hmgu>/Ppp3cc<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppp3cc<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263220	F	MP:0001697	abnormal embryo size	Pptc7<tm1b(EUCOMM)Hmgu>/Pptc7<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pptc7<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263221	M	MP:0002079	increased circulating insulin level	Ppy<tm1b(KOMP)Wtsi>/Ppy<tm1b(KOMP)Wtsi>	C57BL/6N-Ppy<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263221	M	MP:0010088	decreased circulating fructosamine level	Ppy<tm1b(KOMP)Wtsi>/Ppy<tm1b(KOMP)Wtsi>	C57BL/6N-Ppy<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6263222	F	MP:0009142	decreased prepulse inhibition	Prag1<em2(IMPC)Tcp>/Prag1<em2(IMPC)Tcp>	C57BL/6NCrl-Prag1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263222	F	MP:0013278	decreased fasting circulating glucose level	Prag1<em2(IMPC)Tcp>/Prag1<em2(IMPC)Tcp>	C57BL/6NCrl-Prag1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263223	M	MP:0001303	abnormal lens morphology	Prc1<tm1b(EUCOMM)Hmgu>/Prc1<+>	C57BL/6N-Prc1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263223	M	MP:0001289	persistence of hyaloid vascular system	Prc1<tm1b(EUCOMM)Hmgu>/Prc1<+>	C57BL/6N-Prc1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263223	M	MP:0001304	cataract	Prc1<tm1b(EUCOMM)Hmgu>/Prc1<+>	C57BL/6N-Prc1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263223	F	MP:0001325	abnormal retina morphology	Prc1<tm1b(EUCOMM)Hmgu>/Prc1<+>	C57BL/6N-Prc1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263226	F	MP:0004952	increased spleen weight	Prdm13<em1(IMPC)Tcp>/Prdm13<em1(IMPC)Tcp>	C57BL/6NCrl-Prdm13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263226	M	MP:0000689	abnormal spleen morphology	Prdm13<em1(IMPC)Tcp>/Prdm13<em1(IMPC)Tcp>	C57BL/6NCrl-Prdm13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263226	F	MP:0005344	increased circulating bilirubin level	Prdm13<em1(IMPC)Tcp>/Prdm13<em1(IMPC)Tcp>	C57BL/6NCrl-Prdm13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263227	F	MP:0010024	increased total body fat amount	Prdm14<tm1b(EUCOMM)Wtsi>/Prdm14<tm1b(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263227	F	MP:0003795	abnormal bone structure	Prdm14<tm1b(EUCOMM)Wtsi>/Prdm14<tm1b(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263227	F	MP:0001926	female infertility	Prdm14<tm1b(EUCOMM)Wtsi>/Prdm14<tm1b(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263227	F	MP:0010124	decreased bone mineral content	Prdm14<tm1b(EUCOMM)Wtsi>/Prdm14<tm1b(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263227	F	MP:0000063	decreased bone mineral density	Prdm14<tm1b(EUCOMM)Wtsi>/Prdm14<tm1b(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263227	F	MP:0000150	abnormal rib morphology	Prdm14<tm1b(EUCOMM)Wtsi>/Prdm14<tm1b(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263227	F	MP:0003961	decreased lean body mass	Prdm14<tm1b(EUCOMM)Wtsi>/Prdm14<tm1b(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263227	M	MP:0001925	male infertility	Prdm14<tm1b(EUCOMM)Wtsi>/Prdm14<tm1b(EUCOMM)Wtsi>	C57BL/6N-Prdm14<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263228	F	MP:0002060	abnormal skin morphology	Prdm5<em1(IMPC)Tcp>/Prdm5<em1(IMPC)Tcp>	C57BL/6NCrl-Prdm5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263228	F	MP:0008259	abnormal optic disk morphology	Prdm5<em1(IMPC)Tcp>/Prdm5<em1(IMPC)Tcp>	C57BL/6NCrl-Prdm5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263228	M	MP:0001147	small testis	Prdm5<em1(IMPC)Tcp>/Prdm5<em1(IMPC)Tcp>	C57BL/6NCrl-Prdm5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263229	F	MP:0001399	hyperactivity	Prim1<em1(IMPC)J>/Prim1<+>	C57BL/6NJ-Prim1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263230	M	MP:0005562	decreased mean corpuscular hemoglobin	Prkab1<em1(IMPC)J>/Prkab1<em1(IMPC)J>	C57BL/6NJ-Prkab1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263230	M	MP:0002591	decreased mean corpuscular volume	Prkab1<em1(IMPC)J>/Prkab1<em1(IMPC)J>	C57BL/6NJ-Prkab1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263231	M	MP:0000274	enlarged heart	Prkab1<em2(IMPC)Mbp>/Prkab1<em2(IMPC)Mbp>	C57BL/6N-Prkab1<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263231	M	MP:0000266	abnormal heart morphology	Prkab1<em2(IMPC)Mbp>/Prkab1<em2(IMPC)Mbp>	C57BL/6N-Prkab1<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263231	M	MP:0000709	enlarged thymus	Prkab1<em2(IMPC)Mbp>/Prkab1<em2(IMPC)Mbp>	C57BL/6N-Prkab1<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263231	M	MP:0000703	abnormal thymus morphology	Prkab1<em2(IMPC)Mbp>/Prkab1<em2(IMPC)Mbp>	C57BL/6N-Prkab1<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263232	F	MP:0001486	abnormal startle reflex	Prkcsh<tm1.1(KOMP)Vlcg>/Prkcsh<+>	C57BL/6N-Prkcsh<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263234	M	MP:0001488	increased startle reflex	Prkg1<tm1b(KOMP)Wtsi>/Prkg1<+>	C57BL/6N-Prkg1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6263234	M	MP:0000274	enlarged heart	Prkg1<tm1b(KOMP)Wtsi>/Prkg1<+>	C57BL/6N-Prkg1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6263235	F	MP:0002941	increased circulating alanine transaminase level	Prl7b1<tm1.1(KOMP)Vlcg>/Prl7b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Prl7b1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263235	F	MP:0005343	increased circulating aspartate transaminase level	Prl7b1<tm1.1(KOMP)Vlcg>/Prl7b1<tm1.1(KOMP)Vlcg>	C57BL/6N-Prl7b1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263236	M	MP:0000702	enlarged lymph nodes	Prl7d1<em1(IMPC)Tcp>/Prl7d1<em1(IMPC)Tcp>	C57BL/6NCrl-Prl7d1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263240	F	MP:0000274	enlarged heart	Prpf38b<tm1.1(KOMP)Vlcg>/Prpf38b<+>	C57BL/6N-Prpf38b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263240	F	MP:0000266	abnormal heart morphology	Prpf38b<tm1.1(KOMP)Vlcg>/Prpf38b<+>	C57BL/6N-Prpf38b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263241	M	MP:0000219	increased neutrophil cell number	Prpf3<tm1b(KOMP)Wtsi>/Prpf3<+>	C57BL/6N-Prpf3<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263243	F	MP:0001304	cataract	Prpf40a<em1(IMPC)J>/Prpf40a<+>	C57BL/6NJ-Prpf40a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263243	F	MP:0002574	increased vertical activity	Prpf40a<em1(IMPC)J>/Prpf40a<+>	C57BL/6NJ-Prpf40a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263243	M	MP:0002590	increased mean corpuscular volume	Prpf40a<em1(IMPC)J>/Prpf40a<+>	C57BL/6NJ-Prpf40a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263243	M	MP:0002874	decreased hemoglobin content	Prpf40a<em1(IMPC)J>/Prpf40a<+>	C57BL/6NJ-Prpf40a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263243	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Prpf40a<em1(IMPC)J>/Prpf40a<+>	C57BL/6NJ-Prpf40a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263243	M	MP:0002875	decreased erythrocyte cell number	Prpf40a<em1(IMPC)J>/Prpf40a<+>	C57BL/6NJ-Prpf40a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263248	M	MP:0002060	abnormal skin morphology	Prr9<em1(IMPC)Mbp>/Prr9<em1(IMPC)Mbp>	C57BL/6NCrl-Prr9<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263249	M	MP:0001489	decreased startle reflex	Prrt2<tm1b(KOMP)Wtsi>/Prrt2<tm1b(KOMP)Wtsi>	C57BL/6N-Prrt2<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263249	F	MP:0002764	short tibia	Prrt2<tm1b(KOMP)Wtsi>/Prrt2<tm1b(KOMP)Wtsi>	C57BL/6N-Prrt2<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263251	F	MP:0000063	decreased bone mineral density	Prss2<tm1.1(KOMP)Vlcg>/Prss2<tm1.1(KOMP)Vlcg>	C57BL/6N-Prss2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263251	F	MP:0001523	impaired righting response	Prss2<tm1.1(KOMP)Vlcg>/Prss2<tm1.1(KOMP)Vlcg>	C57BL/6N-Prss2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263251	F	MP:0000198	decreased circulating phosphate level	Prss2<tm1.1(KOMP)Vlcg>/Prss2<tm1.1(KOMP)Vlcg>	C57BL/6N-Prss2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263251	F	MP:0010124	decreased bone mineral content	Prss2<tm1.1(KOMP)Vlcg>/Prss2<tm1.1(KOMP)Vlcg>	C57BL/6N-Prss2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263255	F	MP:0006358	absent pinna reflex	Prss53<em2(IMPC)Wtsi>/Prss53<em2(IMPC)Wtsi>	C57BL/6N-Prss53<em2(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6263256	M	MP:0005567	decreased circulating total protein level	Prss53<em3(IMPC)Wtsi>/Prss53<em3(IMPC)Wtsi>	C57BL/6N-Prss53<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263256	M	MP:0005553	increased circulating creatinine level	Prss53<em3(IMPC)Wtsi>/Prss53<em3(IMPC)Wtsi>	C57BL/6N-Prss53<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263256	M	MP:0000221	decreased leukocyte cell number	Prss53<em3(IMPC)Wtsi>/Prss53<em3(IMPC)Wtsi>	C57BL/6N-Prss53<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263256	M	MP:0005419	decreased circulating serum albumin level	Prss53<em3(IMPC)Wtsi>/Prss53<em3(IMPC)Wtsi>	C57BL/6N-Prss53<em3(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263257	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Prss8<tm1b(EUCOMM)Hmgu>/Prss8<+>	C57BL/6N-Prss8<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263257	M	MP:0020870	decreased thigmotaxis	Prss8<tm1b(EUCOMM)Hmgu>/Prss8<+>	C57BL/6N-Prss8<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263257	F	MP:0001304	cataract	Prss8<tm1b(EUCOMM)Hmgu>/Prss8<+>	C57BL/6N-Prss8<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263262	M	MP:0010052	increased grip strength	Psg16<tm1b(KOMP)Mbp>/Psg16<tm1b(KOMP)Mbp>	C57BL/6N-Psg16<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6263264	M	MP:0005179	decreased circulating cholesterol level	Psg20<em1(IMPC)Wtsi>/Psg20<em1(IMPC)Wtsi>	C57BL/6N-Psg20<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263265	M	MP:0002075	abnormal coat/hair pigmentation	Psg26<em1(IMPC)Wtsi>/Psg26<em1(IMPC)Wtsi>	C57BL/6N-Psg26<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263266	M	MP:0002079	increased circulating insulin level	Psg27<em1(IMPC)Wtsi>/Psg27<em1(IMPC)Wtsi>	C57BL/6N-Psg27<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263268	F	MP:0005292	improved glucose tolerance	Pskh1<tm1b(EUCOMM)Wtsi>/Pskh1<+>	C57BL/6N-Pskh1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263268	M	MP:0002833	increased heart weight	Pskh1<tm1b(EUCOMM)Wtsi>/Pskh1<+>	C57BL/6N-Pskh1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263270	M	MP:0005344	increased circulating bilirubin level	Psmc2<tm1b(EUCOMM)Hmgu>/Psmc2<+>	C57BL/6N-Psmc2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263270	F	MP:0002966	decreased circulating alkaline phosphatase level	Psmc2<tm1b(EUCOMM)Hmgu>/Psmc2<+>	C57BL/6N-Psmc2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263272	M	MP:0020870	decreased thigmotaxis	Psmc6<tm1b(KOMP)Wtsi>/Psmc6<+>	C57BL/6N-Psmc6<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263275	M	MP:0002135	abnormal kidney morphology	Psme1<tm1.1(KOMP)Vlcg>/Psme1<tm1.1(KOMP)Vlcg>	C57BL/6N-Psme1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263277	F	MP:0000598	abnormal liver morphology	Pstpip2<em1(IMPC)Tcp>/Pstpip2<em1(IMPC)Tcp>	C57BL/6NCrl-Pstpip2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263277	F	MP:0001417	decreased exploration in new environment	Pstpip2<em1(IMPC)Tcp>/Pstpip2<em1(IMPC)Tcp>	C57BL/6NCrl-Pstpip2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263277	F	MP:0002111	abnormal tail morphology	Pstpip2<em1(IMPC)Tcp>/Pstpip2<em1(IMPC)Tcp>	C57BL/6NCrl-Pstpip2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263277	M	MP:0002968	increased circulating alkaline phosphatase level	Pstpip2<em1(IMPC)Tcp>/Pstpip2<em1(IMPC)Tcp>	C57BL/6NCrl-Pstpip2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263277	M	MP:0005292	improved glucose tolerance	Pstpip2<em1(IMPC)Tcp>/Pstpip2<em1(IMPC)Tcp>	C57BL/6NCrl-Pstpip2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263277	F	MP:0010053	decreased grip strength	Pstpip2<em1(IMPC)Tcp>/Pstpip2<em1(IMPC)Tcp>	C57BL/6NCrl-Pstpip2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263277	M	MP:0002059	abnormal seminal vesicle morphology	Pstpip2<em1(IMPC)Tcp>/Pstpip2<em1(IMPC)Tcp>	C57BL/6NCrl-Pstpip2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263277	F	MP:0000063	decreased bone mineral density	Pstpip2<em1(IMPC)Tcp>/Pstpip2<em1(IMPC)Tcp>	C57BL/6NCrl-Pstpip2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263279	M	MP:0000219	increased neutrophil cell number	Ptch2<tm3b(EUCOMM)Hmgu>/Ptch2<tm3b(EUCOMM)Hmgu>	C57BL/6N-Ptch2<tm3b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263279	M	MP:0005016	decreased lymphocyte cell number	Ptch2<tm3b(EUCOMM)Hmgu>/Ptch2<tm3b(EUCOMM)Hmgu>	C57BL/6N-Ptch2<tm3b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263279	M	MP:0011874	enlarged urinary bladder	Ptch2<tm3b(EUCOMM)Hmgu>/Ptch2<tm3b(EUCOMM)Hmgu>	C57BL/6N-Ptch2<tm3b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263279	M	MP:0013279	increased fasting circulating glucose level	Ptch2<tm3b(EUCOMM)Hmgu>/Ptch2<tm3b(EUCOMM)Hmgu>	C57BL/6N-Ptch2<tm3b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263280	F	MP:0002092	abnormal eye morphology	Ptchd3<em1(IMPC)Mbp>/Ptchd3<em1(IMPC)Mbp>	C57BL/6NCrl-Ptchd3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263280	F	MP:0001293	anophthalmia	Ptchd3<em1(IMPC)Mbp>/Ptchd3<em1(IMPC)Mbp>	C57BL/6NCrl-Ptchd3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263281	M	MP:0000538	abnormal urinary bladder morphology	Ptk6<tm1b(EUCOMM)Wtsi>/Ptk6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ptk6<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6263283	F	MP:0001120	abnormal uterus morphology	Ptp4a1<em2(IMPC)Tcp>/Ptp4a1<em2(IMPC)Tcp>	C57BL/6NCrl-Ptp4a1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263283	F	MP:0002764	short tibia	Ptp4a1<em2(IMPC)Tcp>/Ptp4a1<em2(IMPC)Tcp>	C57BL/6NCrl-Ptp4a1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263283	M	MP:0011874	enlarged urinary bladder	Ptp4a1<em2(IMPC)Tcp>/Ptp4a1<em2(IMPC)Tcp>	C57BL/6NCrl-Ptp4a1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263283	M	MP:0000692	small spleen	Ptp4a1<em2(IMPC)Tcp>/Ptp4a1<em2(IMPC)Tcp>	C57BL/6NCrl-Ptp4a1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263283	F	MP:0002060	abnormal skin morphology	Ptp4a1<em2(IMPC)Tcp>/Ptp4a1<em2(IMPC)Tcp>	C57BL/6NCrl-Ptp4a1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263283	F	MP:0001297	microphthalmia	Ptp4a1<em2(IMPC)Tcp>/Ptp4a1<em2(IMPC)Tcp>	C57BL/6NCrl-Ptp4a1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263283	F	MP:0010124	decreased bone mineral content	Ptp4a1<em2(IMPC)Tcp>/Ptp4a1<em2(IMPC)Tcp>	C57BL/6NCrl-Ptp4a1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263283	F	MP:0000266	abnormal heart morphology	Ptp4a1<em2(IMPC)Tcp>/Ptp4a1<em2(IMPC)Tcp>	C57BL/6NCrl-Ptp4a1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263283	F	MP:0002989	small kidney	Ptp4a1<em2(IMPC)Tcp>/Ptp4a1<em2(IMPC)Tcp>	C57BL/6NCrl-Ptp4a1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263283	F	MP:0003795	abnormal bone structure	Ptp4a1<em2(IMPC)Tcp>/Ptp4a1<em2(IMPC)Tcp>	C57BL/6NCrl-Ptp4a1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263283	F	MP:0000157	abnormal sternum morphology	Ptp4a1<em2(IMPC)Tcp>/Ptp4a1<em2(IMPC)Tcp>	C57BL/6NCrl-Ptp4a1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263283	F	MP:0002968	increased circulating alkaline phosphatase level	Ptp4a1<em2(IMPC)Tcp>/Ptp4a1<em2(IMPC)Tcp>	C57BL/6NCrl-Ptp4a1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263284	F	MP:0010053	decreased grip strength	Ptpra<tm1b(EUCOMM)Hmgu>/Ptpra<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ptpra<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263284	M	MP:0001488	increased startle reflex	Ptpra<tm1b(EUCOMM)Hmgu>/Ptpra<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ptpra<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263285	F	MP:0001415	increased exploration in new environment	Ptprk<em1(IMPC)J>/Ptprk<em1(IMPC)J>	C57BL/6NJ-Ptprk<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263285	M	MP:0002075	abnormal coat/hair pigmentation	Ptprk<em1(IMPC)J>/Ptprk<em1(IMPC)J>	C57BL/6NJ-Ptprk<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263285	F	MP:0001304	cataract	Ptprk<em1(IMPC)J>/Ptprk<em1(IMPC)J>	C57BL/6NJ-Ptprk<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263288	M	MP:0002059	abnormal seminal vesicle morphology	Pttg1<tm1b(EUCOMM)Wtsi>/Pttg1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pttg1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263288	F	MP:0011110	preweaning lethality, incomplete penetrance	Pttg1<tm1b(EUCOMM)Wtsi>/Pttg1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pttg1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263288	F	MP:0000692	small spleen	Pttg1<tm1b(EUCOMM)Wtsi>/Pttg1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pttg1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263288	M	MP:0001147	small testis	Pttg1<tm1b(EUCOMM)Wtsi>/Pttg1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pttg1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263288	M	MP:0002989	small kidney	Pttg1<tm1b(EUCOMM)Wtsi>/Pttg1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pttg1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263288	F	MP:0005278	abnormal cholesterol homeostasis	Pttg1<tm1b(EUCOMM)Wtsi>/Pttg1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pttg1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263288	M	MP:0001552	increased circulating triglyceride level	Pttg1<tm1b(EUCOMM)Wtsi>/Pttg1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pttg1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263289	M	MP:0020870	decreased thigmotaxis	Pudp<tm1.1(KOMP)Vlcg>/Pudp<tm1.1(KOMP)Vlcg>	C57BL/6N-Pudp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263289	F	MP:0013279	increased fasting circulating glucose level	Pudp<tm1.1(KOMP)Vlcg>/Pudp<tm1.1(KOMP)Vlcg>	C57BL/6N-Pudp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263290	M	MP:0010025	decreased total body fat amount	Pum2<tm1b(KOMP)Wtsi>/Pum2<tm1b(KOMP)Wtsi>	C57BL/6N-Pum2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263290	M	MP:0002599	increased mean platelet volume	Pum2<tm1b(KOMP)Wtsi>/Pum2<tm1b(KOMP)Wtsi>	C57BL/6N-Pum2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263290	M	MP:0003960	increased lean body mass	Pum2<tm1b(KOMP)Wtsi>/Pum2<tm1b(KOMP)Wtsi>	C57BL/6N-Pum2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263291	M	MP:0002968	increased circulating alkaline phosphatase level	Pus10<tm1b(EUCOMM)Hmgu>/Pus10<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pus10<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263292	M	MP:0002574	increased vertical activity	Pxdn<em1(IMPC)J>/Pxdn<em1(IMPC)J>	C57BL/6NJ-Pxdn<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263292	M	MP:0010052	increased grip strength	Pxdn<em1(IMPC)J>/Pxdn<em1(IMPC)J>	C57BL/6NJ-Pxdn<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263292	F	MP:0002075	abnormal coat/hair pigmentation	Pxdn<em1(IMPC)J>/Pxdn<em1(IMPC)J>	C57BL/6NJ-Pxdn<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263292	F	MP:0020870	decreased thigmotaxis	Pxdn<em1(IMPC)J>/Pxdn<em1(IMPC)J>	C57BL/6NJ-Pxdn<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263294	M	MP:0005292	improved glucose tolerance	Rab11fip3<em1(IMPC)J>/Rab11fip3<em1(IMPC)J>	C57BL/6NJ-Rab11fip3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263294	M	MP:0001486	abnormal startle reflex	Rab11fip3<em1(IMPC)J>/Rab11fip3<em1(IMPC)J>	C57BL/6NJ-Rab11fip3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263294	F	MP:0004924	abnormal behavior	Rab11fip3<em1(IMPC)J>/Rab11fip3<em1(IMPC)J>	C57BL/6NJ-Rab11fip3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263294	M	MP:0001489	decreased startle reflex	Rab11fip3<em1(IMPC)J>/Rab11fip3<em1(IMPC)J>	C57BL/6NJ-Rab11fip3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263294	F	MP:0020870	decreased thigmotaxis	Rab11fip3<em1(IMPC)J>/Rab11fip3<em1(IMPC)J>	C57BL/6NJ-Rab11fip3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263295	F	MP:0001415	increased exploration in new environment	Rab11fip4<em1(IMPC)J>/Rab11fip4<em1(IMPC)J>	C57BL/6NJ-Rab11fip4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263295	F	MP:0001399	hyperactivity	Rab11fip4<em1(IMPC)J>/Rab11fip4<em1(IMPC)J>	C57BL/6NJ-Rab11fip4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263297	M	MP:0002875	decreased erythrocyte cell number	Rab2a<em2(IMPC)Tcp>/Rab2a<+>	C57BL/6NCrl-Rab2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263297	M	MP:0002590	increased mean corpuscular volume	Rab2a<em2(IMPC)Tcp>/Rab2a<+>	C57BL/6NCrl-Rab2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263297	M	MP:0004952	increased spleen weight	Rab2a<em2(IMPC)Tcp>/Rab2a<+>	C57BL/6NCrl-Rab2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263297	M	MP:0005561	increased mean corpuscular hemoglobin	Rab2a<em2(IMPC)Tcp>/Rab2a<+>	C57BL/6NCrl-Rab2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263297	M	MP:0010067	increased red blood cell distribution width	Rab2a<em2(IMPC)Tcp>/Rab2a<+>	C57BL/6NCrl-Rab2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263299	M	MP:0000470	abnormal stomach morphology	Rab39b<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Rab39b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263299	M	MP:0011874	enlarged urinary bladder	Rab39b<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Rab39b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263299	M	MP:0002060	abnormal skin morphology	Rab39b<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Rab39b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263299	M	MP:0002834	decreased heart weight	Rab39b<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Rab39b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263299	M	MP:0004953	decreased spleen weight	Rab39b<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Rab39b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263300	F	MP:0001127	small ovary	Rab39b<em1(IMPC)Tcp>/Rab39b<em1(IMPC)Tcp>	C57BL/6NCrl-Rab39b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263300	F	MP:0009709	hydrometra	Rab39b<em1(IMPC)Tcp>/Rab39b<em1(IMPC)Tcp>	C57BL/6NCrl-Rab39b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263300	F	MP:0004738	abnormal auditory brainstem response	Rab39b<em1(IMPC)Tcp>/Rab39b<em1(IMPC)Tcp>	C57BL/6NCrl-Rab39b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263300	F	MP:0000745	tremors	Rab39b<em1(IMPC)Tcp>/Rab39b<em1(IMPC)Tcp>	C57BL/6NCrl-Rab39b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263300	F	MP:0000598	abnormal liver morphology	Rab39b<em1(IMPC)Tcp>/Rab39b<em1(IMPC)Tcp>	C57BL/6NCrl-Rab39b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263300	F	MP:0020420	abnormal freezing behavior	Rab39b<em1(IMPC)Tcp>/Rab39b<em1(IMPC)Tcp>	C57BL/6NCrl-Rab39b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263300	F	MP:0005343	increased circulating aspartate transaminase level	Rab39b<em1(IMPC)Tcp>/Rab39b<em1(IMPC)Tcp>	C57BL/6NCrl-Rab39b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263301	M	MP:0000186	decreased circulating HDL cholesterol level	Rab3gap2<tm1b(KOMP)Wtsi>/Rab3gap2<tm1b(KOMP)Wtsi>	C57BL/6N-Rab3gap2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263301	M	MP:0000208	decreased hematocrit	Rab3gap2<tm1b(KOMP)Wtsi>/Rab3gap2<tm1b(KOMP)Wtsi>	C57BL/6N-Rab3gap2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263301	M	MP:0003179	thrombocytopenia	Rab3gap2<tm1b(KOMP)Wtsi>/Rab3gap2<tm1b(KOMP)Wtsi>	C57BL/6N-Rab3gap2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263301	M	MP:0002968	increased circulating alkaline phosphatase level	Rab3gap2<tm1b(KOMP)Wtsi>/Rab3gap2<tm1b(KOMP)Wtsi>	C57BL/6N-Rab3gap2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263301	M	MP:0005333	decreased heart rate	Rab3gap2<tm1b(KOMP)Wtsi>/Rab3gap2<tm1b(KOMP)Wtsi>	C57BL/6N-Rab3gap2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263301	M	MP:0010506	prolonged RR interval	Rab3gap2<tm1b(KOMP)Wtsi>/Rab3gap2<tm1b(KOMP)Wtsi>	C57BL/6N-Rab3gap2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263301	M	MP:0005344	increased circulating bilirubin level	Rab3gap2<tm1b(KOMP)Wtsi>/Rab3gap2<tm1b(KOMP)Wtsi>	C57BL/6N-Rab3gap2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263301	F	MP:0000443	abnormal snout morphology	Rab3gap2<tm1b(KOMP)Wtsi>/Rab3gap2<tm1b(KOMP)Wtsi>	C57BL/6N-Rab3gap2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263301	F	MP:0008259	abnormal optic disk morphology	Rab3gap2<tm1b(KOMP)Wtsi>/Rab3gap2<tm1b(KOMP)Wtsi>	C57BL/6N-Rab3gap2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263301	M	MP:0005287	narrow eye opening	Rab3gap2<tm1b(KOMP)Wtsi>/Rab3gap2<tm1b(KOMP)Wtsi>	C57BL/6N-Rab3gap2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263302	M	MP:0010506	prolonged RR interval	Rab4a<tm1b(EUCOMM)Hmgu>/Rab4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rab4a<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263302	M	MP:0005333	decreased heart rate	Rab4a<tm1b(EUCOMM)Hmgu>/Rab4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rab4a<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263303	F	MP:0005553	increased circulating creatinine level	Rab4b<em1(IMPC)J>/Rab4b<em1(IMPC)J>	C57BL/6NJ-Rab4b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263303	F	MP:0002968	increased circulating alkaline phosphatase level	Rab4b<em1(IMPC)J>/Rab4b<em1(IMPC)J>	C57BL/6NJ-Rab4b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263304	F	MP:0001488	increased startle reflex	Rab5b<em1(IMPC)J>/Rab5b<em1(IMPC)J>	C57BL/6NJ-Rab5b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263304	F	MP:0002574	increased vertical activity	Rab5b<em1(IMPC)J>/Rab5b<em1(IMPC)J>	C57BL/6NJ-Rab5b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263305	F	MP:0010053	decreased grip strength	Rab6b<em1(IMPC)J>/Rab6b<em1(IMPC)J>	C57BL/6NJ-Rab6b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263305	F	MP:0009142	decreased prepulse inhibition	Rab6b<em1(IMPC)J>/Rab6b<em1(IMPC)J>	C57BL/6NJ-Rab6b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263306	M	MP:0003961	decreased lean body mass	Rab8a<em1(IMPC)J>/Rab8a<+>	C57BL/6NJ-Rab8a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263306	F	MP:0010052	increased grip strength	Rab8a<em1(IMPC)J>/Rab8a<+>	C57BL/6NJ-Rab8a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263307	M	MP:0002079	increased circulating insulin level	Rabl2<tm1.1(KOMP)Wtsi>/Rabl2<tm1.1(KOMP)Wtsi>	C57BL/6N-Rabl2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263307	M	MP:0002981	increased liver weight	Rabl2<tm1.1(KOMP)Wtsi>/Rabl2<tm1.1(KOMP)Wtsi>	C57BL/6N-Rabl2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263307	F	MP:0010024	increased total body fat amount	Rabl2<tm1.1(KOMP)Wtsi>/Rabl2<tm1.1(KOMP)Wtsi>	C57BL/6N-Rabl2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263307	M	MP:0001147	small testis	Rabl2<tm1.1(KOMP)Wtsi>/Rabl2<tm1.1(KOMP)Wtsi>	C57BL/6N-Rabl2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263307	M	MP:0001146	abnormal testis morphology	Rabl2<tm1.1(KOMP)Wtsi>/Rabl2<tm1.1(KOMP)Wtsi>	C57BL/6N-Rabl2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263307	F	MP:0010124	decreased bone mineral content	Rabl2<tm1.1(KOMP)Wtsi>/Rabl2<tm1.1(KOMP)Wtsi>	C57BL/6N-Rabl2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263307	M	MP:0005293	impaired glucose tolerance	Rabl2<tm1.1(KOMP)Wtsi>/Rabl2<tm1.1(KOMP)Wtsi>	C57BL/6N-Rabl2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263307	F	MP:0001926	female infertility	Rabl2<tm1.1(KOMP)Wtsi>/Rabl2<tm1.1(KOMP)Wtsi>	C57BL/6N-Rabl2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263307	F	MP:0000063	decreased bone mineral density	Rabl2<tm1.1(KOMP)Wtsi>/Rabl2<tm1.1(KOMP)Wtsi>	C57BL/6N-Rabl2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263307	F	MP:0003961	decreased lean body mass	Rabl2<tm1.1(KOMP)Wtsi>/Rabl2<tm1.1(KOMP)Wtsi>	C57BL/6N-Rabl2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263307	F	MP:0006203	eye hemorrhage	Rabl2<tm1.1(KOMP)Wtsi>/Rabl2<tm1.1(KOMP)Wtsi>	C57BL/6N-Rabl2<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263308	M	MP:0001417	decreased exploration in new environment	Radil<em1(IMPC)Tcp>/Radil<em1(IMPC)Tcp>	C57BL/6NCrl-Radil<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263308	F	MP:0000689	abnormal spleen morphology	Radil<em1(IMPC)Tcp>/Radil<em1(IMPC)Tcp>	C57BL/6NCrl-Radil<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263311	M	MP:0001785	edema	Rai14<em1(IMPC)J>/Rai14<em1(IMPC)J>	C57BL/6NJ-Rai14<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263311	M	MP:0001575	cyanosis	Rai14<em1(IMPC)J>/Rai14<em1(IMPC)J>	C57BL/6NJ-Rai14<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263312	M	MP:0001552	increased circulating triglyceride level	Raly<em2(IMPC)Tcp>/Raly<em2(IMPC)Tcp>	C57BL/6NCrl-Raly<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263312	F	MP:0001175	abnormal lung morphology	Raly<em2(IMPC)Tcp>/Raly<em2(IMPC)Tcp>	C57BL/6NCrl-Raly<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263312	F	MP:0001944	abnormal pancreas morphology	Raly<em2(IMPC)Tcp>/Raly<em2(IMPC)Tcp>	C57BL/6NCrl-Raly<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263313	M	MP:0000266	abnormal heart morphology	Ranbp10<tm1.1(KOMP)Vlcg>/Ranbp10<tm1.1(KOMP)Vlcg>	C57BL/6N-Ranbp10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263313	M	MP:0005559	increased circulating glucose level	Ranbp10<tm1.1(KOMP)Vlcg>/Ranbp10<tm1.1(KOMP)Vlcg>	C57BL/6N-Ranbp10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263313	M	MP:0000274	enlarged heart	Ranbp10<tm1.1(KOMP)Vlcg>/Ranbp10<tm1.1(KOMP)Vlcg>	C57BL/6N-Ranbp10<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263314	F	MP:0005655	increased aggression	Rap1gap2<tm1b(EUCOMM)Hmgu>/Rap1gap2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rap1gap2<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263314	M	MP:0001566	increased circulating phosphate level	Rap1gap2<tm1b(EUCOMM)Hmgu>/Rap1gap2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rap1gap2<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263314	M	MP:0002833	increased heart weight	Rap1gap2<tm1b(EUCOMM)Hmgu>/Rap1gap2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rap1gap2<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263316	M	MP:0001147	small testis	Rapgef5<em1(IMPC)H>/Rapgef5<em1(IMPC)H>	C57BL/6N-Rapgef5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263319	F	MP:0011396	abnormal sleep behavior	Rasa3<tm1b(KOMP)J>/Rasa3<+>	C57BL/6N-Rasa3<tm1b(KOMP)J>/J	N	MGI:5576271
MGI:6263322	M	MP:0001258	decreased body length	Rasal3<tm1b(EUCOMM)Hmgu>/Rasal3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rasal3<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263322	M	MP:0001552	increased circulating triglyceride level	Rasal3<tm1b(EUCOMM)Hmgu>/Rasal3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rasal3<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263322	M	MP:0002764	short tibia	Rasal3<tm1b(EUCOMM)Hmgu>/Rasal3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rasal3<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263322	F	MP:0005016	decreased lymphocyte cell number	Rasal3<tm1b(EUCOMM)Hmgu>/Rasal3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rasal3<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263322	F	MP:0005554	decreased circulating creatinine level	Rasal3<tm1b(EUCOMM)Hmgu>/Rasal3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rasal3<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263322	F	MP:0005011	increased eosinophil cell number	Rasal3<tm1b(EUCOMM)Hmgu>/Rasal3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rasal3<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263322	F	MP:0011960	abnormal eye anterior chamber depth	Rasal3<tm1b(EUCOMM)Hmgu>/Rasal3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rasal3<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263323	M	MP:0002135	abnormal kidney morphology	Rbbp4<em1(IMPC)Mbp>/Rbbp4<+>	C57BL/6NCrl-Rbbp4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263323	M	MP:0001417	decreased exploration in new environment	Rbbp4<em1(IMPC)Mbp>/Rbbp4<+>	C57BL/6NCrl-Rbbp4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263323	F	MP:0000601	small liver	Rbbp4<em1(IMPC)Mbp>/Rbbp4<+>	C57BL/6NCrl-Rbbp4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263323	M	MP:0003068	enlarged kidney	Rbbp4<em1(IMPC)Mbp>/Rbbp4<+>	C57BL/6NCrl-Rbbp4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263323	F	MP:0005084	abnormal gallbladder morphology	Rbbp4<em1(IMPC)Mbp>/Rbbp4<+>	C57BL/6NCrl-Rbbp4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263323	F	MP:0010123	increased bone mineral content	Rbbp4<em1(IMPC)Mbp>/Rbbp4<+>	C57BL/6NCrl-Rbbp4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263323	F	MP:0000691	enlarged spleen	Rbbp4<em1(IMPC)Mbp>/Rbbp4<+>	C57BL/6NCrl-Rbbp4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263323	F	MP:0000689	abnormal spleen morphology	Rbbp4<em1(IMPC)Mbp>/Rbbp4<+>	C57BL/6NCrl-Rbbp4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263326	M	MP:0002764	short tibia	Rbfox1<tm1b(KOMP)Wtsi>/Rbfox1<+>	C57BL/6N-Rbfox1<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263328	M	MP:0002135	abnormal kidney morphology	Rbl1<tm1b(EUCOMM)Hmgu>/Rbl1<+>	C57BL/6N-Rbl1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263328	F	MP:0010393	shortened QRS complex duration	Rbl1<tm1b(EUCOMM)Hmgu>/Rbl1<+>	C57BL/6N-Rbl1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263330	F	MP:0001325	abnormal retina morphology	Rbl2<tm1b(EUCOMM)Hmgu>/Rbl2<+>	C57BL/6N-Rbl2<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263330	F	MP:0001289	persistence of hyaloid vascular system	Rbl2<tm1b(EUCOMM)Hmgu>/Rbl2<+>	C57BL/6N-Rbl2<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263330	M	MP:0001556	increased circulating HDL cholesterol level	Rbl2<tm1b(EUCOMM)Hmgu>/Rbl2<+>	C57BL/6N-Rbl2<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263330	M	MP:0005178	increased circulating cholesterol level	Rbl2<tm1b(EUCOMM)Hmgu>/Rbl2<+>	C57BL/6N-Rbl2<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263332	F	MP:0002092	abnormal eye morphology	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	F	MP:0001120	abnormal uterus morphology	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	M	MP:0002833	increased heart weight	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	M	MP:0002060	abnormal skin morphology	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	M	MP:0000274	enlarged heart	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	M	MP:0002631	abnormal epididymis morphology	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	M	MP:0000266	abnormal heart morphology	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	M	MP:0001147	small testis	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	M	MP:0004931	enlarged epididymis	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	F	MP:0001126	abnormal ovary morphology	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	F	MP:0009709	hydrometra	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	F	MP:0010123	increased bone mineral content	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	F	MP:0003271	abnormal duodenum morphology	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	F	MP:0000702	enlarged lymph nodes	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	F	MP:0002339	abnormal lymph node morphology	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	M	MP:0000689	abnormal spleen morphology	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263332	M	MP:0001146	abnormal testis morphology	Rbm22<em1(IMPC)Mbp>/Rbm22<+>	C57BL/6NCrl-Rbm22<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263334	M	MP:0001489	decreased startle reflex	Rbm22<tm1.1(KOMP)Vlcg>/Rbm22<+>	C57BL/6N-Rbm22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263334	M	MP:0000062	increased bone mineral density	Rbm22<tm1.1(KOMP)Vlcg>/Rbm22<+>	C57BL/6N-Rbm22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263340	F	MP:0002574	increased vertical activity	Rbm4b<tm1.1(KOMP)Vlcg>/Rbm4b<tm1.1(KOMP)Vlcg>	C57BL/6N-Rbm4b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263340	M	MP:0005344	increased circulating bilirubin level	Rbm4b<tm1.1(KOMP)Vlcg>/Rbm4b<tm1.1(KOMP)Vlcg>	C57BL/6N-Rbm4b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263340	F	MP:0011396	abnormal sleep behavior	Rbm4b<tm1.1(KOMP)Vlcg>/Rbm4b<tm1.1(KOMP)Vlcg>	C57BL/6N-Rbm4b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263340	M	MP:0001759	increased urine glucose level	Rbm4b<tm1.1(KOMP)Vlcg>/Rbm4b<tm1.1(KOMP)Vlcg>	C57BL/6N-Rbm4b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263341	M	MP:0000274	enlarged heart	Rbms1<tm1b(EUCOMM)Wtsi>/Rbms1<+>	C57BL/6N-Rbms1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263341	M	MP:0000367	abnormal coat/ hair morphology	Rbms1<tm1b(EUCOMM)Wtsi>/Rbms1<+>	C57BL/6N-Rbms1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263341	F	MP:0002968	increased circulating alkaline phosphatase level	Rbms1<tm1b(EUCOMM)Wtsi>/Rbms1<+>	C57BL/6N-Rbms1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263341	M	MP:0005293	impaired glucose tolerance	Rbms1<tm1b(EUCOMM)Wtsi>/Rbms1<+>	C57BL/6N-Rbms1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263344	F	MP:0010053	decreased grip strength	Rbp1<tm2b(EUCOMM)Hmgu>/Rbp1<tm2b(EUCOMM)Hmgu>	C57BL/6N-Rbp1<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263345	M	MP:0005344	increased circulating bilirubin level	Rbpj<tm1b(EUCOMM)Hmgu>/Rbpj<+>	C57BL/6N-Rbpj<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263345	F	MP:0000063	decreased bone mineral density	Rbpj<tm1b(EUCOMM)Hmgu>/Rbpj<+>	C57BL/6N-Rbpj<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263345	F	MP:0005292	improved glucose tolerance	Rbpj<tm1b(EUCOMM)Hmgu>/Rbpj<+>	C57BL/6N-Rbpj<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263346	F	MP:0003961	decreased lean body mass	Rbpms2<em1(IMPC)J>/Rbpms2<em1(IMPC)J>	C57BL/6NJ-Rbpms2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263346	F	MP:0001926	female infertility	Rbpms2<em1(IMPC)J>/Rbpms2<em1(IMPC)J>	C57BL/6NJ-Rbpms2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263346	F	MP:0002075	abnormal coat/hair pigmentation	Rbpms2<em1(IMPC)J>/Rbpms2<em1(IMPC)J>	C57BL/6NJ-Rbpms2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263346	F	MP:0010124	decreased bone mineral content	Rbpms2<em1(IMPC)J>/Rbpms2<em1(IMPC)J>	C57BL/6NJ-Rbpms2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263346	F	MP:0003795	abnormal bone structure	Rbpms2<em1(IMPC)J>/Rbpms2<em1(IMPC)J>	C57BL/6NJ-Rbpms2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263346	F	MP:0010024	increased total body fat amount	Rbpms2<em1(IMPC)J>/Rbpms2<em1(IMPC)J>	C57BL/6NJ-Rbpms2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263346	F	MP:0000063	decreased bone mineral density	Rbpms2<em1(IMPC)J>/Rbpms2<em1(IMPC)J>	C57BL/6NJ-Rbpms2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263347	F	MP:0010025	decreased total body fat amount	Rcan1<tm1b(KOMP)Wtsi>/Rcan1<tm1b(KOMP)Wtsi>	C57BL/6N-Rcan1<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263347	F	MP:0003960	increased lean body mass	Rcan1<tm1b(KOMP)Wtsi>/Rcan1<tm1b(KOMP)Wtsi>	C57BL/6N-Rcan1<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263348	M	MP:0001406	abnormal gait	Rccd1<tm1.1(KOMP)Wtsi>/Rccd1<tm1.1(KOMP)Wtsi>	C57BL/6N-Rccd1<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263349	M	MP:0010097	abnormal retina blood vessel morphology	Rcn1<tm1b(EUCOMM)Hmgu>/Rcn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rcn1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263349	F	MP:0002764	short tibia	Rcn1<tm1b(EUCOMM)Hmgu>/Rcn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rcn1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263349	M	MP:0001289	persistence of hyaloid vascular system	Rcn1<tm1b(EUCOMM)Hmgu>/Rcn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rcn1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263349	F	MP:0002968	increased circulating alkaline phosphatase level	Rcn1<tm1b(EUCOMM)Hmgu>/Rcn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rcn1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263350	M	MP:0001785	edema	Rcn3<tm1b(EUCOMM)Hmgu>/Rcn3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rcn3<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263351	M	MP:0005343	increased circulating aspartate transaminase level	Rec8<tm1b(KOMP)Wtsi>/Rec8<tm1b(KOMP)Wtsi>	C57BL/6N-Rec8<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263351	M	MP:0001556	increased circulating HDL cholesterol level	Rec8<tm1b(KOMP)Wtsi>/Rec8<tm1b(KOMP)Wtsi>	C57BL/6N-Rec8<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263351	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Rec8<tm1b(KOMP)Wtsi>/Rec8<tm1b(KOMP)Wtsi>	C57BL/6N-Rec8<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263351	M	MP:0005178	increased circulating cholesterol level	Rec8<tm1b(KOMP)Wtsi>/Rec8<tm1b(KOMP)Wtsi>	C57BL/6N-Rec8<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263351	M	MP:0001925	male infertility	Rec8<tm1b(KOMP)Wtsi>/Rec8<tm1b(KOMP)Wtsi>	C57BL/6N-Rec8<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263352	M	MP:0003960	increased lean body mass	Reg3d<tm1b(EUCOMM)Wtsi>/Reg3d<tm1b(EUCOMM)Wtsi>	C57BL/6N-Reg3d<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263353	M	MP:0010123	increased bone mineral content	Rep15<em1(IMPC)Tcp>/Rep15<em1(IMPC)Tcp>	C57BL/6NCrl-Rep15<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263353	M	MP:0010025	decreased total body fat amount	Rep15<em1(IMPC)Tcp>/Rep15<em1(IMPC)Tcp>	C57BL/6NCrl-Rep15<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263353	M	MP:0000062	increased bone mineral density	Rep15<em1(IMPC)Tcp>/Rep15<em1(IMPC)Tcp>	C57BL/6NCrl-Rep15<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263354	M	MP:0001304	cataract	Reps2<em1(IMPC)J>/Y	C57BL/6NJ-Reps2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263355	M	MP:0004924	abnormal behavior	Rer1<tm1.1(KOMP)Vlcg>/Rer1<+>	C57BL/6N-Rer1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263355	F	MP:0003795	abnormal bone structure	Rer1<tm1.1(KOMP)Vlcg>/Rer1<+>	C57BL/6N-Rer1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263355	F	MP:0010124	decreased bone mineral content	Rer1<tm1.1(KOMP)Vlcg>/Rer1<+>	C57BL/6N-Rer1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263355	F	MP:0001399	hyperactivity	Rer1<tm1.1(KOMP)Vlcg>/Rer1<+>	C57BL/6N-Rer1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263357	M	MP:0001925	male infertility	Resf1<em1(IMPC)Mbp>/Resf1<em1(IMPC)Mbp>	C57BL/6NCrl-Resf1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263357	F	MP:0002092	abnormal eye morphology	Resf1<em1(IMPC)Mbp>/Resf1<em1(IMPC)Mbp>	C57BL/6NCrl-Resf1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263357	F	MP:0001926	female infertility	Resf1<em1(IMPC)Mbp>/Resf1<em1(IMPC)Mbp>	C57BL/6NCrl-Resf1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263358	F	MP:0001304	cataract	Rev3l<tm1b(EUCOMM)Hmgu>/Rev3l<+>	C57BL/6N-Rev3l<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263358	F	MP:0005566	decreased blood urea nitrogen level	Rev3l<tm1b(EUCOMM)Hmgu>/Rev3l<+>	C57BL/6N-Rev3l<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263358	F	MP:0005554	decreased circulating creatinine level	Rev3l<tm1b(EUCOMM)Hmgu>/Rev3l<+>	C57BL/6N-Rev3l<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263362	F	MP:0005564	increased hemoglobin content	Rft1<tm1b(KOMP)Wtsi>/Rft1<+>	C57BL/6N-Rft1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263362	F	MP:0004357	long tibia	Rft1<tm1b(KOMP)Wtsi>/Rft1<+>	C57BL/6N-Rft1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263362	M	MP:0002875	decreased erythrocyte cell number	Rft1<tm1b(KOMP)Wtsi>/Rft1<+>	C57BL/6N-Rft1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263362	F	MP:0002606	increased basophil cell number	Rft1<tm1b(KOMP)Wtsi>/Rft1<+>	C57BL/6N-Rft1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263362	M	MP:0000220	increased monocyte cell number	Rft1<tm1b(KOMP)Wtsi>/Rft1<+>	C57BL/6N-Rft1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263362	M	MP:0005016	decreased lymphocyte cell number	Rft1<tm1b(KOMP)Wtsi>/Rft1<+>	C57BL/6N-Rft1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263364	M	MP:0001925	male infertility	Rfx8<tm1b(EUCOMM)Hmgu>/Rfx8<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rfx8<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263364	F	MP:0001926	female infertility	Rfx8<tm1b(EUCOMM)Hmgu>/Rfx8<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rfx8<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263365	M	MP:0002968	increased circulating alkaline phosphatase level	Rfxank<tm1b(EUCOMM)Hmgu>/Rfxank<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rfxank<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263365	M	MP:0001417	decreased exploration in new environment	Rfxank<tm1b(EUCOMM)Hmgu>/Rfxank<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rfxank<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263366	F	MP:0002966	decreased circulating alkaline phosphatase level	Rgl3<em1(IMPC)H>/Rgl3<em1(IMPC)H>	C57BL/6NTac-Rgl3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263366	M	MP:0001406	abnormal gait	Rgl3<em1(IMPC)H>/Rgl3<em1(IMPC)H>	C57BL/6NTac-Rgl3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263366	F	MP:0000195	decreased circulating calcium level	Rgl3<em1(IMPC)H>/Rgl3<em1(IMPC)H>	C57BL/6NTac-Rgl3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263370	F	MP:0000063	decreased bone mineral density	Rhbdf1<tm1.1(KOMP)Vlcg>/Rhbdf1<+>	C57BL/6N-Rhbdf1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263370	F	MP:0010052	increased grip strength	Rhbdf1<tm1.1(KOMP)Vlcg>/Rhbdf1<+>	C57BL/6N-Rhbdf1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263373	M	MP:0006243	impaired pupillary reflex	Ric8a<tm1b(KOMP)Wtsi>/Ric8a<+>	C57BL/6N-Ric8a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263373	M	MP:0010024	increased total body fat amount	Ric8a<tm1b(KOMP)Wtsi>/Ric8a<+>	C57BL/6N-Ric8a<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263374	F	MP:0000208	decreased hematocrit	Rida<tm1a(KOMP)Wtsi>/Rida<tm1a(KOMP)Wtsi>	C57BL/6N-Rida<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263377	M	MP:0002060	abnormal skin morphology	Rnase1<em5(IMPC)Tcp>/Rnase1<em5(IMPC)Tcp>	C57BL/6NCrl-Rnase1<em5(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263380	F	MP:0003795	abnormal bone structure	Rnf10<em1(IMPC)J>/Rnf10<em1(IMPC)J>	C57BL/6NJ-Rnf10<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263380	F	MP:0002574	increased vertical activity	Rnf10<em1(IMPC)J>/Rnf10<em1(IMPC)J>	C57BL/6NJ-Rnf10<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263380	F	MP:0001513	limb grasping	Rnf10<em1(IMPC)J>/Rnf10<em1(IMPC)J>	C57BL/6NJ-Rnf10<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263380	F	MP:0001417	decreased exploration in new environment	Rnf10<em1(IMPC)J>/Rnf10<em1(IMPC)J>	C57BL/6NJ-Rnf10<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263380	F	MP:0010123	increased bone mineral content	Rnf10<em1(IMPC)J>/Rnf10<em1(IMPC)J>	C57BL/6NJ-Rnf10<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263381	F	MP:0002941	increased circulating alanine transaminase level	Rnf10<em1(IMPC)Mbp>/Rnf10<em1(IMPC)Mbp>	C57BL/6N-Rnf10<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263381	M	MP:0002135	abnormal kidney morphology	Rnf10<em1(IMPC)Mbp>/Rnf10<em1(IMPC)Mbp>	C57BL/6N-Rnf10<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263381	F	MP:0002092	abnormal eye morphology	Rnf10<em1(IMPC)Mbp>/Rnf10<em1(IMPC)Mbp>	C57BL/6N-Rnf10<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263381	M	MP:0002175	decreased brain weight	Rnf10<em1(IMPC)Mbp>/Rnf10<em1(IMPC)Mbp>	C57BL/6N-Rnf10<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263381	F	MP:0001293	anophthalmia	Rnf10<em1(IMPC)Mbp>/Rnf10<em1(IMPC)Mbp>	C57BL/6N-Rnf10<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263381	F	MP:0005343	increased circulating aspartate transaminase level	Rnf10<em1(IMPC)Mbp>/Rnf10<em1(IMPC)Mbp>	C57BL/6N-Rnf10<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263381	F	MP:0005559	increased circulating glucose level	Rnf10<em1(IMPC)Mbp>/Rnf10<em1(IMPC)Mbp>	C57BL/6N-Rnf10<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263382	F	MP:0004952	increased spleen weight	Rnf115<em1(IMPC)H>/Rnf115<em1(IMPC)H>	C57BL/6N-Rnf115<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263382	F	MP:0001402	decreased locomotor activity	Rnf115<em1(IMPC)H>/Rnf115<em1(IMPC)H>	C57BL/6N-Rnf115<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263382	F	MP:0001417	decreased exploration in new environment	Rnf115<em1(IMPC)H>/Rnf115<em1(IMPC)H>	C57BL/6N-Rnf115<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263383	M	MP:0000157	abnormal sternum morphology	Rnf135<em1(IMPC)Tcp>/Rnf135<em1(IMPC)Tcp>	C57BL/6NCrl-Rnf135<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263383	F	MP:0001127	small ovary	Rnf135<em1(IMPC)Tcp>/Rnf135<em1(IMPC)Tcp>	C57BL/6NCrl-Rnf135<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263383	F	MP:0010053	decreased grip strength	Rnf135<em1(IMPC)Tcp>/Rnf135<em1(IMPC)Tcp>	C57BL/6NCrl-Rnf135<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263383	F	MP:0001417	decreased exploration in new environment	Rnf135<em1(IMPC)Tcp>/Rnf135<em1(IMPC)Tcp>	C57BL/6NCrl-Rnf135<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263383	F	MP:0002637	small uterus	Rnf135<em1(IMPC)Tcp>/Rnf135<em1(IMPC)Tcp>	C57BL/6NCrl-Rnf135<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263383	M	MP:0000470	abnormal stomach morphology	Rnf135<em1(IMPC)Tcp>/Rnf135<em1(IMPC)Tcp>	C57BL/6NCrl-Rnf135<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263383	F	MP:0000702	enlarged lymph nodes	Rnf135<em1(IMPC)Tcp>/Rnf135<em1(IMPC)Tcp>	C57BL/6NCrl-Rnf135<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263384	F	MP:0003020	decreased circulating chloride level	Rnf144a<em1(IMPC)Tcp>/Rnf144a<em1(IMPC)Tcp>	C57BL/6NCrl-Rnf144a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263385	M	MP:0002875	decreased erythrocyte cell number	Rnf24<em1(IMPC)J>/Rnf24<em1(IMPC)J>	C57BL/6NJ-Rnf24<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263385	M	MP:0002874	decreased hemoglobin content	Rnf24<em1(IMPC)J>/Rnf24<em1(IMPC)J>	C57BL/6NJ-Rnf24<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263387	F	MP:0002941	increased circulating alanine transaminase level	Rp9<tm1b(EUCOMM)Wtsi>/Rp9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rp9<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6263387	F	MP:0009709	hydrometra	Rp9<tm1b(EUCOMM)Wtsi>/Rp9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rp9<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6263387	F	MP:0009142	decreased prepulse inhibition	Rp9<tm1b(EUCOMM)Wtsi>/Rp9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rp9<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6263387	F	MP:0001258	decreased body length	Rp9<tm1b(EUCOMM)Wtsi>/Rp9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rp9<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6263387	F	MP:0001120	abnormal uterus morphology	Rp9<tm1b(EUCOMM)Wtsi>/Rp9<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rp9<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:6263389	F	MP:0010067	increased red blood cell distribution width	Rpl32<tm1b(EUCOMM)Hmgu>/Rpl32<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rpl32<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263392	F	MP:0005343	increased circulating aspartate transaminase level	Rps26<tm2b(EUCOMM)Hmgu>/Rps26<tm2b(EUCOMM)Hmgu>	C57BL/6N-Rps26<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263392	M	MP:0001488	increased startle reflex	Rps26<tm2b(EUCOMM)Hmgu>/Rps26<tm2b(EUCOMM)Hmgu>	C57BL/6N-Rps26<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263393	M	MP:0001489	decreased startle reflex	Rps6ka1<em1(IMPC)J>/Rps6ka1<em1(IMPC)J>	C57BL/6NJ-Rps6ka1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263394	M	MP:0000195	decreased circulating calcium level	Rreb1<tm1b(EUCOMM)Wtsi>/Rreb1<+>	C57BL/6N-Rreb1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263394	M	MP:0000208	decreased hematocrit	Rreb1<tm1b(EUCOMM)Wtsi>/Rreb1<+>	C57BL/6N-Rreb1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263394	M	MP:0003960	increased lean body mass	Rreb1<tm1b(EUCOMM)Wtsi>/Rreb1<+>	C57BL/6N-Rreb1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263394	M	MP:0005419	decreased circulating serum albumin level	Rreb1<tm1b(EUCOMM)Wtsi>/Rreb1<+>	C57BL/6N-Rreb1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263394	M	MP:0010025	decreased total body fat amount	Rreb1<tm1b(EUCOMM)Wtsi>/Rreb1<+>	C57BL/6N-Rreb1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263394	M	MP:0002874	decreased hemoglobin content	Rreb1<tm1b(EUCOMM)Wtsi>/Rreb1<+>	C57BL/6N-Rreb1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263394	M	MP:0010067	increased red blood cell distribution width	Rreb1<tm1b(EUCOMM)Wtsi>/Rreb1<+>	C57BL/6N-Rreb1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263394	M	MP:0002875	decreased erythrocyte cell number	Rreb1<tm1b(EUCOMM)Wtsi>/Rreb1<+>	C57BL/6N-Rreb1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263395	F	MP:0011100	preweaning lethality, complete penetrance	Rrm1<tm1.1(NCOM)Mfgc>/Rrm1<tm1.1(NCOM)Mfgc>	C57BL/6N-Rrm1<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:6263396	M	MP:0010053	decreased grip strength	Rrs1<tm1.1(KOMP)Vlcg>/Rrs1<+>	C57BL/6N-Rrs1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263396	F	MP:0001399	hyperactivity	Rrs1<tm1.1(KOMP)Vlcg>/Rrs1<+>	C57BL/6N-Rrs1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263399	M	MP:0002968	increased circulating alkaline phosphatase level	Rspo1<tm2b(KOMP)Wtsi>/Rspo1<tm2b(KOMP)Wtsi>	C57BL/6N-Rspo1<tm2b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263399	F	MP:0011960	abnormal eye anterior chamber depth	Rspo1<tm2b(KOMP)Wtsi>/Rspo1<tm2b(KOMP)Wtsi>	C57BL/6N-Rspo1<tm2b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263399	F	MP:0003961	decreased lean body mass	Rspo1<tm2b(KOMP)Wtsi>/Rspo1<tm2b(KOMP)Wtsi>	C57BL/6N-Rspo1<tm2b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263399	F	MP:0005013	increased lymphocyte cell number	Rspo1<tm2b(KOMP)Wtsi>/Rspo1<tm2b(KOMP)Wtsi>	C57BL/6N-Rspo1<tm2b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263399	F	MP:0005553	increased circulating creatinine level	Rspo1<tm2b(KOMP)Wtsi>/Rspo1<tm2b(KOMP)Wtsi>	C57BL/6N-Rspo1<tm2b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263399	F	MP:0002699	abnormal vitreous body morphology	Rspo1<tm2b(KOMP)Wtsi>/Rspo1<tm2b(KOMP)Wtsi>	C57BL/6N-Rspo1<tm2b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263399	F	MP:0003731	abnormal retina outer nuclear layer morphology	Rspo1<tm2b(KOMP)Wtsi>/Rspo1<tm2b(KOMP)Wtsi>	C57BL/6N-Rspo1<tm2b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263405	F	MP:0000689	abnormal spleen morphology	Rttn<em1(IMPC)Tcp>/Rttn<+>	C57BL/6NCrl-Rttn<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263405	M	MP:0011874	enlarged urinary bladder	Rttn<em1(IMPC)Tcp>/Rttn<+>	C57BL/6NCrl-Rttn<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263405	F	MP:0010124	decreased bone mineral content	Rttn<em1(IMPC)Tcp>/Rttn<+>	C57BL/6NCrl-Rttn<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263405	M	MP:0000470	abnormal stomach morphology	Rttn<em1(IMPC)Tcp>/Rttn<+>	C57BL/6NCrl-Rttn<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263405	F	MP:0002188	small heart	Rttn<em1(IMPC)Tcp>/Rttn<+>	C57BL/6NCrl-Rttn<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263405	M	MP:0000598	abnormal liver morphology	Rttn<em1(IMPC)Tcp>/Rttn<+>	C57BL/6NCrl-Rttn<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263405	F	MP:0002060	abnormal skin morphology	Rttn<em1(IMPC)Tcp>/Rttn<+>	C57BL/6NCrl-Rttn<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263407	F	MP:0000186	decreased circulating HDL cholesterol level	Rundc1<tm1a(EUCOMM)Wtsi>/Rundc1<+>	C57BL/6N-Rundc1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263408	F	MP:0001392	abnormal locomotor behavior	Runx3<tm1b(KOMP)Wtsi>/Runx3<+>	C57BL/6N-Runx3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263410	M	MP:0010025	decreased total body fat amount	Rusc1<em1(IMPC)J>/Rusc1<em1(IMPC)J>	C57BL/6NJ-Rusc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263410	F	MP:0002591	decreased mean corpuscular volume	Rusc1<em1(IMPC)J>/Rusc1<em1(IMPC)J>	C57BL/6NJ-Rusc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263410	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Rusc1<em1(IMPC)J>/Rusc1<em1(IMPC)J>	C57BL/6NJ-Rusc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263410	F	MP:0010124	decreased bone mineral content	Rusc1<em1(IMPC)J>/Rusc1<em1(IMPC)J>	C57BL/6NJ-Rusc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263410	M	MP:0001289	persistence of hyaloid vascular system	Rusc1<em1(IMPC)J>/Rusc1<em1(IMPC)J>	C57BL/6NJ-Rusc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263414	F	MP:0001926	female infertility	S1pr3<tm1b(EUCOMM)Wtsi>/S1pr3<tm1b(EUCOMM)Wtsi>	C57BL/6N-S1pr3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263414	M	MP:0001325	abnormal retina morphology	S1pr3<tm1b(EUCOMM)Wtsi>/S1pr3<tm1b(EUCOMM)Wtsi>	C57BL/6N-S1pr3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263414	F	MP:0011239	abnormal skin coloration	S1pr3<tm1b(EUCOMM)Wtsi>/S1pr3<tm1b(EUCOMM)Wtsi>	C57BL/6N-S1pr3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263414	M	MP:0001925	male infertility	S1pr3<tm1b(EUCOMM)Wtsi>/S1pr3<tm1b(EUCOMM)Wtsi>	C57BL/6N-S1pr3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263414	M	MP:0010097	abnormal retina blood vessel morphology	S1pr3<tm1b(EUCOMM)Wtsi>/S1pr3<tm1b(EUCOMM)Wtsi>	C57BL/6N-S1pr3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263415	M	MP:0002135	abnormal kidney morphology	Sacs<em1(IMPC)Tcp>/Sacs<+>	C57BL/6NCrl-Sacs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263415	M	MP:0001488	increased startle reflex	Sacs<em1(IMPC)Tcp>/Sacs<+>	C57BL/6NCrl-Sacs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263415	M	MP:0002060	abnormal skin morphology	Sacs<em1(IMPC)Tcp>/Sacs<+>	C57BL/6NCrl-Sacs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263416	M	MP:0011100	preweaning lethality, complete penetrance	Sacs<em1(IMPC)Tcp>/Sacs<em1(IMPC)Tcp>	C57BL/6NCrl-Sacs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263416	F	MP:0000689	abnormal spleen morphology	Sacs<em1(IMPC)Tcp>/Sacs<em1(IMPC)Tcp>	C57BL/6NCrl-Sacs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263416	F	MP:0002590	increased mean corpuscular volume	Sacs<em1(IMPC)Tcp>/Sacs<em1(IMPC)Tcp>	C57BL/6NCrl-Sacs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263416	F	MP:0000157	abnormal sternum morphology	Sacs<em1(IMPC)Tcp>/Sacs<em1(IMPC)Tcp>	C57BL/6NCrl-Sacs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263416	F	MP:0002637	small uterus	Sacs<em1(IMPC)Tcp>/Sacs<em1(IMPC)Tcp>	C57BL/6NCrl-Sacs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263419	M	MP:0005292	improved glucose tolerance	Sars1<tm1.1(KOMP)Vlcg>/Sars1<+>	C57BL/6N-Sars1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263419	F	MP:0010053	decreased grip strength	Sars1<tm1.1(KOMP)Vlcg>/Sars1<+>	C57BL/6N-Sars1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263421	M	MP:0020870	decreased thigmotaxis	Sart1<tm1.1(KOMP)Vlcg>/Sart1<+>	C57BL/6N-Sart1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263421	M	MP:0013278	decreased fasting circulating glucose level	Sart1<tm1.1(KOMP)Vlcg>/Sart1<+>	C57BL/6N-Sart1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263421	M	MP:0004924	abnormal behavior	Sart1<tm1.1(KOMP)Vlcg>/Sart1<+>	C57BL/6N-Sart1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263423	F	MP:0002590	increased mean corpuscular volume	Satb2<em3(IMPC)Tcp>/Satb2<+>	C57BL/6NCrl-Satb2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263423	F	MP:0002968	increased circulating alkaline phosphatase level	Satb2<em3(IMPC)Tcp>/Satb2<+>	C57BL/6NCrl-Satb2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263423	F	MP:0001325	abnormal retina morphology	Satb2<em3(IMPC)Tcp>/Satb2<+>	C57BL/6NCrl-Satb2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263425	F	MP:0002699	abnormal vitreous body morphology	Saxo1<tm1b(EUCOMM)Hmgu>/Saxo1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Saxo1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6263425	F	MP:0001399	hyperactivity	Saxo1<tm1b(EUCOMM)Hmgu>/Saxo1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Saxo1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6263425	F	MP:0005016	decreased lymphocyte cell number	Saxo1<tm1b(EUCOMM)Hmgu>/Saxo1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Saxo1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6263425	F	MP:0001258	decreased body length	Saxo1<tm1b(EUCOMM)Hmgu>/Saxo1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Saxo1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6263425	F	MP:0005011	increased eosinophil cell number	Saxo1<tm1b(EUCOMM)Hmgu>/Saxo1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Saxo1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6263426	F	MP:0011960	abnormal eye anterior chamber depth	Sbk1<tm1b(EUCOMM)Wtsi>/Sbk1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sbk1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263427	M	MP:0000218	increased leukocyte cell number	Sbno1<tm1b(EUCOMM)Hmgu>/Sbno1<+>	C57BL/6N-Sbno1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263427	M	MP:0001510	abnormal coat appearance	Sbno1<tm1b(EUCOMM)Hmgu>/Sbno1<+>	C57BL/6N-Sbno1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263427	M	MP:0010067	increased red blood cell distribution width	Sbno1<tm1b(EUCOMM)Hmgu>/Sbno1<+>	C57BL/6N-Sbno1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263427	F	MP:0010087	increased circulating fructosamine level	Sbno1<tm1b(EUCOMM)Hmgu>/Sbno1<+>	C57BL/6N-Sbno1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263427	M	MP:0002075	abnormal coat/hair pigmentation	Sbno1<tm1b(EUCOMM)Hmgu>/Sbno1<+>	C57BL/6N-Sbno1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263429	F	MP:0003036	vertebral transformation	Scaf11<em1(IMPC)Wtsi>/Scaf11<em1(IMPC)Wtsi>	C57BL/6N-Scaf11<em1(IMPC)Wtsi>/WtsiCnrm	N	MGI:5576271
MGI:6263429	F	MP:0010124	decreased bone mineral content	Scaf11<em1(IMPC)Wtsi>/Scaf11<em1(IMPC)Wtsi>	C57BL/6N-Scaf11<em1(IMPC)Wtsi>/WtsiCnrm	N	MGI:5576271
MGI:6263429	F	MP:0003795	abnormal bone structure	Scaf11<em1(IMPC)Wtsi>/Scaf11<em1(IMPC)Wtsi>	C57BL/6N-Scaf11<em1(IMPC)Wtsi>/WtsiCnrm	N	MGI:5576271
MGI:6263430	M	MP:0003960	increased lean body mass	Scamp5<tm1.1(KOMP)Vlcg>/Scamp5<+>	C57BL/6N-Scamp5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263430	M	MP:0002959	increased urine microalbumin level	Scamp5<tm1.1(KOMP)Vlcg>/Scamp5<+>	C57BL/6N-Scamp5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263430	F	MP:0011396	abnormal sleep behavior	Scamp5<tm1.1(KOMP)Vlcg>/Scamp5<+>	C57BL/6N-Scamp5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263430	M	MP:0002941	increased circulating alanine transaminase level	Scamp5<tm1.1(KOMP)Vlcg>/Scamp5<+>	C57BL/6N-Scamp5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263432	M	MP:0005566	decreased blood urea nitrogen level	Scaper<tm1b(EUCOMM)Hmgu>/Scaper<tm1b(EUCOMM)Hmgu>	C57BL/6N-Scaper<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6263432	M	MP:0001925	male infertility	Scaper<tm1b(EUCOMM)Hmgu>/Scaper<tm1b(EUCOMM)Hmgu>	C57BL/6N-Scaper<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6263433	F	MP:0000219	increased neutrophil cell number	Scarb2<em2(IMPC)Tcp>/Scarb2<em2(IMPC)Tcp>	C57BL/6NCrl-Scarb2<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263433	M	MP:0000702	enlarged lymph nodes	Scarb2<em2(IMPC)Tcp>/Scarb2<em2(IMPC)Tcp>	C57BL/6NCrl-Scarb2<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263433	F	MP:0000218	increased leukocyte cell number	Scarb2<em2(IMPC)Tcp>/Scarb2<em2(IMPC)Tcp>	C57BL/6NCrl-Scarb2<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263433	F	MP:0005565	increased blood urea nitrogen level	Scarb2<em2(IMPC)Tcp>/Scarb2<em2(IMPC)Tcp>	C57BL/6NCrl-Scarb2<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263433	F	MP:0002591	decreased mean corpuscular volume	Scarb2<em2(IMPC)Tcp>/Scarb2<em2(IMPC)Tcp>	C57BL/6NCrl-Scarb2<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263433	M	MP:0003960	increased lean body mass	Scarb2<em2(IMPC)Tcp>/Scarb2<em2(IMPC)Tcp>	C57BL/6NCrl-Scarb2<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263433	F	MP:0000194	increased circulating calcium level	Scarb2<em2(IMPC)Tcp>/Scarb2<em2(IMPC)Tcp>	C57BL/6NCrl-Scarb2<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263433	M	MP:0003068	enlarged kidney	Scarb2<em2(IMPC)Tcp>/Scarb2<em2(IMPC)Tcp>	C57BL/6NCrl-Scarb2<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263433	F	MP:0004122	abnormal sinus arrhythmia	Scarb2<em2(IMPC)Tcp>/Scarb2<em2(IMPC)Tcp>	C57BL/6NCrl-Scarb2<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263433	F	MP:0005505	thrombocytosis	Scarb2<em2(IMPC)Tcp>/Scarb2<em2(IMPC)Tcp>	C57BL/6NCrl-Scarb2<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263433	M	MP:0011110	preweaning lethality, incomplete penetrance	Scarb2<em2(IMPC)Tcp>/Scarb2<em2(IMPC)Tcp>	C57BL/6NCrl-Scarb2<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263434	F	MP:0002092	abnormal eye morphology	Scin<em1(IMPC)Mbp>/Scin<em1(IMPC)Mbp>	C57BL/6NCrl-Scin<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263436	F	MP:0001406	abnormal gait	Scn4b<em1(IMPC)Wtsi>/Scn4b<em1(IMPC)Wtsi>	C57BL/6N-Scn4b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263441	F	MP:0000367	abnormal coat/ hair morphology	Sdr42e1<em1(IMPC)J>/Sdr42e1<em1(IMPC)J>	C57BL/6NJ-Sdr42e1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263442	M	MP:0002941	increased circulating alanine transaminase level	Sdsl<tm1b(EUCOMM)Hmgu>/Sdsl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sdsl<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6263442	F	MP:0003795	abnormal bone structure	Sdsl<tm1b(EUCOMM)Hmgu>/Sdsl<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sdsl<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6263443	M	MP:0013279	increased fasting circulating glucose level	Sebox<em1(IMPC)J>/Sebox<em1(IMPC)J>	C57BL/6NJ-Sebox<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263444	F	MP:0001402	decreased locomotor activity	Sec11c<tm1b(EUCOMM)Wtsi>/Sec11c<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sec11c<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263447	F	MP:0002079	increased circulating insulin level	Sec61b<em1(IMPC)Mbp>/Sec61b<em1(IMPC)Mbp>	C57BL/6NCrl-Sec61b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263447	F	MP:0001399	hyperactivity	Sec61b<em1(IMPC)Mbp>/Sec61b<em1(IMPC)Mbp>	C57BL/6NCrl-Sec61b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263447	F	MP:0001126	abnormal ovary morphology	Sec61b<em1(IMPC)Mbp>/Sec61b<em1(IMPC)Mbp>	C57BL/6NCrl-Sec61b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263448	M	MP:0002098	abnormal vibrissa morphology	Sec63<tm1b(EUCOMM)Hmgu>/Sec63<+>	C57BL/6N-Sec63<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263448	F	MP:0002941	increased circulating alanine transaminase level	Sec63<tm1b(EUCOMM)Hmgu>/Sec63<+>	C57BL/6N-Sec63<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263448	M	MP:0000219	increased neutrophil cell number	Sec63<tm1b(EUCOMM)Hmgu>/Sec63<+>	C57BL/6N-Sec63<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263448	M	MP:0001284	absent vibrissae	Sec63<tm1b(EUCOMM)Hmgu>/Sec63<+>	C57BL/6N-Sec63<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263448	M	MP:0005016	decreased lymphocyte cell number	Sec63<tm1b(EUCOMM)Hmgu>/Sec63<+>	C57BL/6N-Sec63<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263450	F	MP:0002590	increased mean corpuscular volume	Selenbp1<tm1b(KOMP)Wtsi>/Selenbp1<tm1b(KOMP)Wtsi>	C57BL/6N-Selenbp1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263450	M	MP:0005419	decreased circulating serum albumin level	Selenbp1<tm1b(KOMP)Wtsi>/Selenbp1<tm1b(KOMP)Wtsi>	C57BL/6N-Selenbp1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263450	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Selenbp1<tm1b(KOMP)Wtsi>/Selenbp1<tm1b(KOMP)Wtsi>	C57BL/6N-Selenbp1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263450	F	MP:0002966	decreased circulating alkaline phosphatase level	Selenbp1<tm1b(KOMP)Wtsi>/Selenbp1<tm1b(KOMP)Wtsi>	C57BL/6N-Selenbp1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263450	M	MP:0005554	decreased circulating creatinine level	Selenbp1<tm1b(KOMP)Wtsi>/Selenbp1<tm1b(KOMP)Wtsi>	C57BL/6N-Selenbp1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263450	F	MP:0002079	increased circulating insulin level	Selenbp1<tm1b(KOMP)Wtsi>/Selenbp1<tm1b(KOMP)Wtsi>	C57BL/6N-Selenbp1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263452	F	MP:0000198	decreased circulating phosphate level	Septin3<tm1b(KOMP)Wtsi>/Septin3<+>	C57BL/6N-Septin3<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6263452	F	MP:0001392	abnormal locomotor behavior	Septin3<tm1b(KOMP)Wtsi>/Septin3<+>	C57BL/6N-Septin3<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6263453	M	MP:0009453	enhanced contextual conditioning behavior	Serac1<em1(IMPC)Tcp>/Serac1<em1(IMPC)Tcp>	C57BL/6NCrl-Serac1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263453	M	MP:0000702	enlarged lymph nodes	Serac1<em1(IMPC)Tcp>/Serac1<em1(IMPC)Tcp>	C57BL/6NCrl-Serac1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263453	F	MP:0001126	abnormal ovary morphology	Serac1<em1(IMPC)Tcp>/Serac1<em1(IMPC)Tcp>	C57BL/6NCrl-Serac1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263453	M	MP:0020421	increased freezing behavior	Serac1<em1(IMPC)Tcp>/Serac1<em1(IMPC)Tcp>	C57BL/6NCrl-Serac1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263455	F	MP:0001399	hyperactivity	Serpinb2<tm1b(EUCOMM)Wtsi>/Serpinb2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Serpinb2<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263455	M	MP:0005178	increased circulating cholesterol level	Serpinb2<tm1b(EUCOMM)Wtsi>/Serpinb2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Serpinb2<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263455	M	MP:0001304	cataract	Serpinb2<tm1b(EUCOMM)Wtsi>/Serpinb2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Serpinb2<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263455	M	MP:0005553	increased circulating creatinine level	Serpinb2<tm1b(EUCOMM)Wtsi>/Serpinb2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Serpinb2<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263455	M	MP:0001556	increased circulating HDL cholesterol level	Serpinb2<tm1b(EUCOMM)Wtsi>/Serpinb2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Serpinb2<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263456	M	MP:0002059	abnormal seminal vesicle morphology	Serpinb3d<em1(IMPC)Tcp>/Serpinb3d<em1(IMPC)Tcp>	C57BL/6NCrl-Serpinb3d<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263458	F	MP:0001289	persistence of hyaloid vascular system	Sesn1<tm1b(EUCOMM)Wtsi>/Sesn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sesn1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263458	F	MP:0005561	increased mean corpuscular hemoglobin	Sesn1<tm1b(EUCOMM)Wtsi>/Sesn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sesn1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263458	F	MP:0002590	increased mean corpuscular volume	Sesn1<tm1b(EUCOMM)Wtsi>/Sesn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sesn1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263458	F	MP:0008259	abnormal optic disk morphology	Sesn1<tm1b(EUCOMM)Wtsi>/Sesn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sesn1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263458	M	MP:0005655	increased aggression	Sesn1<tm1b(EUCOMM)Wtsi>/Sesn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sesn1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263460	F	MP:0003984	embryonic growth retardation	Sfr1<em1(IMPC)Mbp>/Sfr1<em1(IMPC)Mbp>	C57BL/6NCrl-Sfr1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263461	F	MP:0010053	decreased grip strength	Sfxn1<tm1b(EUCOMM)Wtsi>/Sfxn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sfxn1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263461	M	MP:0005505	thrombocytosis	Sfxn1<tm1b(EUCOMM)Wtsi>/Sfxn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sfxn1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263461	F	MP:0013279	increased fasting circulating glucose level	Sfxn1<tm1b(EUCOMM)Wtsi>/Sfxn1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sfxn1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263462	M	MP:0002079	increased circulating insulin level	Sfxn3<tm1b(KOMP)Wtsi>/Sfxn3<tm1b(KOMP)Wtsi>	C57BL/6N-Sfxn3<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263464	M	MP:0005344	increased circulating bilirubin level	Sh3bp4<tm1a(EUCOMM)Wtsi>/Sh3bp4<tm1a(EUCOMM)Wtsi>	C57BL/6N-Sh3bp4<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263465	F	MP:0003233	prolonged QT interval	Sh3tc1<tm1b(EUCOMM)Hmgu>/Sh3tc1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sh3tc1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263465	F	MP:0002699	abnormal vitreous body morphology	Sh3tc1<tm1b(EUCOMM)Hmgu>/Sh3tc1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sh3tc1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263465	M	MP:0000220	increased monocyte cell number	Sh3tc1<tm1b(EUCOMM)Hmgu>/Sh3tc1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sh3tc1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263465	F	MP:0005140	decreased cardiac muscle contractility	Sh3tc1<tm1b(EUCOMM)Hmgu>/Sh3tc1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sh3tc1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263465	M	MP:0002644	decreased circulating triglyceride level	Sh3tc1<tm1b(EUCOMM)Hmgu>/Sh3tc1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sh3tc1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263465	F	MP:0005344	increased circulating bilirubin level	Sh3tc1<tm1b(EUCOMM)Hmgu>/Sh3tc1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sh3tc1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263465	M	MP:0000219	increased neutrophil cell number	Sh3tc1<tm1b(EUCOMM)Hmgu>/Sh3tc1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sh3tc1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263467	F	MP:0001399	hyperactivity	Shisa4<tm1b(KOMP)Wtsi>/Shisa4<tm1b(KOMP)Wtsi>	C57BL/6N-Shisa4<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263467	F	MP:0004924	abnormal behavior	Shisa4<tm1b(KOMP)Wtsi>/Shisa4<tm1b(KOMP)Wtsi>	C57BL/6N-Shisa4<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263467	F	MP:0020870	decreased thigmotaxis	Shisa4<tm1b(KOMP)Wtsi>/Shisa4<tm1b(KOMP)Wtsi>	C57BL/6N-Shisa4<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263468	M	MP:0000745	tremors	Shisa7<em1(IMPC)J>/Shisa7<em1(IMPC)J>	C57BL/6NJ-Shisa7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263468	F	MP:0001304	cataract	Shisa7<em1(IMPC)J>/Shisa7<em1(IMPC)J>	C57BL/6NJ-Shisa7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263468	M	MP:0010025	decreased total body fat amount	Shisa7<em1(IMPC)J>/Shisa7<em1(IMPC)J>	C57BL/6NJ-Shisa7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263468	F	MP:0002574	increased vertical activity	Shisa7<em1(IMPC)J>/Shisa7<em1(IMPC)J>	C57BL/6NJ-Shisa7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263470	M	MP:0002060	abnormal skin morphology	Shprh<em1(IMPC)Tcp>/Shprh<em1(IMPC)Tcp>	C57BL/6NCrl-Shprh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263470	M	MP:0000709	enlarged thymus	Shprh<em1(IMPC)Tcp>/Shprh<em1(IMPC)Tcp>	C57BL/6NCrl-Shprh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263470	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Shprh<em1(IMPC)Tcp>/Shprh<em1(IMPC)Tcp>	C57BL/6NCrl-Shprh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263471	F	MP:0002092	abnormal eye morphology	Shroom2<em1(IMPC)Mbp>/Shroom2<em1(IMPC)Mbp>	C57BL/6NCrl-Shroom2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263471	F	MP:0002060	abnormal skin morphology	Shroom2<em1(IMPC)Mbp>/Shroom2<em1(IMPC)Mbp>	C57BL/6NCrl-Shroom2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263472	M	MP:0003917	increased kidney weight	Siglec1<tm1.1(KOMP)Vlcg>/Siglec1<tm1.1(KOMP)Vlcg>	C57BL/6N-Siglec1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263472	M	MP:0005630	increased lung weight	Siglec1<tm1.1(KOMP)Vlcg>/Siglec1<tm1.1(KOMP)Vlcg>	C57BL/6N-Siglec1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263473	M	MP:0000274	enlarged heart	Sik2<em1(IMPC)Mbp>/Sik2<em1(IMPC)Mbp>	C57BL/6N-Sik2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263474	F	MP:0001325	abnormal retina morphology	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0000186	decreased circulating HDL cholesterol level	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0003179	thrombocytopenia	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0004974	decreased regulatory T cell number	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0005633	increased circulating sodium level	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	F	MP:0008806	increased circulating amylase level	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0002599	increased mean platelet volume	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0003960	increased lean body mass	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0000160	kyphosis	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0005628	decreased circulating potassium level	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0005270	abnormal zygomatic bone morphology	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0010088	decreased circulating fructosamine level	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0005179	decreased circulating cholesterol level	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0000195	decreased circulating calcium level	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0002875	decreased erythrocyte cell number	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0008045	decreased NK cell number	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	F	MP:0001312	abnormal cornea morphology	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0010067	increased red blood cell distribution width	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0010025	decreased total body fat amount	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0005292	improved glucose tolerance	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	F	MP:0001926	female infertility	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	F	MP:0005018	decreased T cell number	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263474	M	MP:0000208	decreased hematocrit	Sik3<tm1a(EUCOMM)Hmgu>/Sik3<tm1a(EUCOMM)Hmgu>	C57BL/6N-Sik3<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263476	F	MP:0005016	decreased lymphocyte cell number	Slc13a3<tm1b(KOMP)Wtsi>/Slc13a3<tm1b(KOMP)Wtsi>	C57BL/6N-Slc13a3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263476	M	MP:0000220	increased monocyte cell number	Slc13a3<tm1b(KOMP)Wtsi>/Slc13a3<tm1b(KOMP)Wtsi>	C57BL/6N-Slc13a3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263476	F	MP:0000219	increased neutrophil cell number	Slc13a3<tm1b(KOMP)Wtsi>/Slc13a3<tm1b(KOMP)Wtsi>	C57BL/6N-Slc13a3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263477	M	MP:0002764	short tibia	Slc13a5<tm1b(EUCOMM)Hmgu>/Slc13a5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc13a5<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263483	F	MP:0009476	enlarged cecum	Slc22a4<tm1.1(KOMP)Vlcg>/Slc22a4<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc22a4<tm1.1(KOMP)Vlcg>/Ieg	N	MGI:5576271
MGI:6263484	M	MP:0001175	abnormal lung morphology	Slc23a3<em1(IMPC)Tcp>/Slc23a3<em1(IMPC)Tcp>	C57BL/6NCrl-Slc23a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263485	M	MP:0010052	increased grip strength	Slc25a10<tm1b(EUCOMM)Wtsi>/Slc25a10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc25a10<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263485	F	MP:0011965	decreased total retina thickness	Slc25a10<tm1b(EUCOMM)Wtsi>/Slc25a10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc25a10<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263485	F	MP:0010097	abnormal retina blood vessel morphology	Slc25a10<tm1b(EUCOMM)Wtsi>/Slc25a10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc25a10<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263485	F	MP:0008806	increased circulating amylase level	Slc25a10<tm1b(EUCOMM)Wtsi>/Slc25a10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc25a10<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263487	M	MP:0001417	decreased exploration in new environment	Slc25a15<tm1b(EUCOMM)Hmgu>/Slc25a15<+>	C57BL/6N-Slc25a15<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263489	F	MP:0001293	anophthalmia	Slc25a1<tm1b(EUCOMM)Wtsi>/Slc25a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc25a1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263492	F	MP:0013279	increased fasting circulating glucose level	Slc25a46<em1(IMPC)J>/Slc25a46<+>	C57BL/6NJ-Slc25a46<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263492	F	MP:0010053	decreased grip strength	Slc25a46<em1(IMPC)J>/Slc25a46<+>	C57BL/6NJ-Slc25a46<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263493	F	MP:0011110	preweaning lethality, incomplete penetrance	Slc25a47<tm1b(EUCOMM)Hmgu>/Slc25a47<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc25a47<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263494	F	MP:0020870	decreased thigmotaxis	Slc26a10<em1(IMPC)J>/Slc26a10<em1(IMPC)J>	C57BL/6NJ-Slc26a10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263494	F	MP:0004924	abnormal behavior	Slc26a10<em1(IMPC)J>/Slc26a10<em1(IMPC)J>	C57BL/6NJ-Slc26a10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263495	M	MP:0010090	increased circulating creatine kinase level	Slc28a3<em1(IMPC)H>/Slc28a3<em1(IMPC)H>	C57BL/6N-Slc28a3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263495	F	MP:0000220	increased monocyte cell number	Slc28a3<em1(IMPC)H>/Slc28a3<em1(IMPC)H>	C57BL/6N-Slc28a3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263496	M	MP:0020421	increased freezing behavior	Slc2a13<em1(IMPC)Mbp>/Slc2a13<em1(IMPC)Mbp>	C57BL/6NCrl-Slc2a13<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263496	M	MP:0005293	impaired glucose tolerance	Slc2a13<em1(IMPC)Mbp>/Slc2a13<em1(IMPC)Mbp>	C57BL/6NCrl-Slc2a13<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263497	F	MP:0000367	abnormal coat/ hair morphology	Slc35c2<tm1.1(KOMP)Vlcg>/Slc35c2<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc35c2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263497	F	MP:0004924	abnormal behavior	Slc35c2<tm1.1(KOMP)Vlcg>/Slc35c2<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc35c2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263497	F	MP:0020870	decreased thigmotaxis	Slc35c2<tm1.1(KOMP)Vlcg>/Slc35c2<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc35c2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263499	F	MP:0011960	abnormal eye anterior chamber depth	Slc37a1<tm1b(EUCOMM)Hmgu>/Slc37a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc37a1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263499	F	MP:0005344	increased circulating bilirubin level	Slc37a1<tm1b(EUCOMM)Hmgu>/Slc37a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc37a1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263499	M	MP:0000266	abnormal heart morphology	Slc37a1<tm1b(EUCOMM)Hmgu>/Slc37a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc37a1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263499	M	MP:0000598	abnormal liver morphology	Slc37a1<tm1b(EUCOMM)Hmgu>/Slc37a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc37a1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6263500	F	MP:0000266	abnormal heart morphology	Slc38a11<tm2b(KOMP)Mbp>/Slc38a11<tm2b(KOMP)Mbp>	C57BL/6N-Slc38a11<tm2b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6263500	F	MP:0000274	enlarged heart	Slc38a11<tm2b(KOMP)Mbp>/Slc38a11<tm2b(KOMP)Mbp>	C57BL/6N-Slc38a11<tm2b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6263502	M	MP:0013279	increased fasting circulating glucose level	Slc39a4<tm1.1(KOMP)Wtsi>/Slc39a4<+>	C57BL/6N-Slc39a4<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0003960	increased lean body mass	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0010025	decreased total body fat amount	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0004952	increased spleen weight	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0000691	enlarged spleen	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0010123	increased bone mineral content	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0001556	increased circulating HDL cholesterol level	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0011874	enlarged urinary bladder	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	F	MP:0005011	increased eosinophil cell number	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0009552	urinary bladder obstruction	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0003917	increased kidney weight	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0002968	increased circulating alkaline phosphatase level	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0005178	increased circulating cholesterol level	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0000689	abnormal spleen morphology	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0002591	decreased mean corpuscular volume	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263503	M	MP:0003068	enlarged kidney	Slc3a1<tm1.1(KOMP)Vlcg>/Slc3a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc3a1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263505	F	MP:0001486	abnormal startle reflex	Slc44a2<em1(IMPC)J>/Slc44a2<em1(IMPC)J>	C57BL/6NJ-Slc44a2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263506	M	MP:0002699	abnormal vitreous body morphology	Slc44a3<tm1b(EUCOMM)Wtsi>/Slc44a3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc44a3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263506	M	MP:0010097	abnormal retina blood vessel morphology	Slc44a3<tm1b(EUCOMM)Wtsi>/Slc44a3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc44a3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263506	M	MP:0002968	increased circulating alkaline phosphatase level	Slc44a3<tm1b(EUCOMM)Wtsi>/Slc44a3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc44a3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263506	M	MP:0001417	decreased exploration in new environment	Slc44a3<tm1b(EUCOMM)Wtsi>/Slc44a3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc44a3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263507	M	MP:0005344	increased circulating bilirubin level	Slc44a4<tm1b(EUCOMM)Hmgu>/Slc44a4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc44a4<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263507	F	MP:0009142	decreased prepulse inhibition	Slc44a4<tm1b(EUCOMM)Hmgu>/Slc44a4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc44a4<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263508	M	MP:0005568	increased circulating total protein level	Slc47a1<tm1b(EUCOMM)Wtsi>/Slc47a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc47a1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263508	M	MP:0000198	decreased circulating phosphate level	Slc47a1<tm1b(EUCOMM)Wtsi>/Slc47a1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Slc47a1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263509	M	MP:0001488	increased startle reflex	Slc4a10<tm1b(KOMP)Wtsi>/Slc4a10<tm1b(KOMP)Wtsi>	C57BL/6N-Slc4a10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6263509	F	MP:0005564	increased hemoglobin content	Slc4a10<tm1b(KOMP)Wtsi>/Slc4a10<tm1b(KOMP)Wtsi>	C57BL/6N-Slc4a10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6263509	F	MP:0010124	decreased bone mineral content	Slc4a10<tm1b(KOMP)Wtsi>/Slc4a10<tm1b(KOMP)Wtsi>	C57BL/6N-Slc4a10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6263509	M	MP:0000692	small spleen	Slc4a10<tm1b(KOMP)Wtsi>/Slc4a10<tm1b(KOMP)Wtsi>	C57BL/6N-Slc4a10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6263509	F	MP:0001399	hyperactivity	Slc4a10<tm1b(KOMP)Wtsi>/Slc4a10<tm1b(KOMP)Wtsi>	C57BL/6N-Slc4a10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6263509	M	MP:0001406	abnormal gait	Slc4a10<tm1b(KOMP)Wtsi>/Slc4a10<tm1b(KOMP)Wtsi>	C57BL/6N-Slc4a10<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6263510	F	MP:0010067	increased red blood cell distribution width	Slc51b<em1(IMPC)Mbp>/Slc51b<em1(IMPC)Mbp>	C57BL/6NCrl-Slc51b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263510	F	MP:0002968	increased circulating alkaline phosphatase level	Slc51b<em1(IMPC)Mbp>/Slc51b<em1(IMPC)Mbp>	C57BL/6NCrl-Slc51b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263510	F	MP:0009709	hydrometra	Slc51b<em1(IMPC)Mbp>/Slc51b<em1(IMPC)Mbp>	C57BL/6NCrl-Slc51b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263510	F	MP:0000691	enlarged spleen	Slc51b<em1(IMPC)Mbp>/Slc51b<em1(IMPC)Mbp>	C57BL/6NCrl-Slc51b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263510	F	MP:0000689	abnormal spleen morphology	Slc51b<em1(IMPC)Mbp>/Slc51b<em1(IMPC)Mbp>	C57BL/6NCrl-Slc51b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263510	M	MP:0010025	decreased total body fat amount	Slc51b<em1(IMPC)Mbp>/Slc51b<em1(IMPC)Mbp>	C57BL/6NCrl-Slc51b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263510	M	MP:0003960	increased lean body mass	Slc51b<em1(IMPC)Mbp>/Slc51b<em1(IMPC)Mbp>	C57BL/6NCrl-Slc51b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263512	F	MP:0009142	decreased prepulse inhibition	Slc5a5<tm1b(KOMP)Wtsi>/Slc5a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc5a5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263512	F	MP:0011471	decreased urine creatinine level	Slc5a5<tm1b(KOMP)Wtsi>/Slc5a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc5a5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263512	F	MP:0011396	abnormal sleep behavior	Slc5a5<tm1b(KOMP)Wtsi>/Slc5a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc5a5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263512	F	MP:0001406	abnormal gait	Slc5a5<tm1b(KOMP)Wtsi>/Slc5a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc5a5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263512	F	MP:0000745	tremors	Slc5a5<tm1b(KOMP)Wtsi>/Slc5a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc5a5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263512	F	MP:0000063	decreased bone mineral density	Slc5a5<tm1b(KOMP)Wtsi>/Slc5a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc5a5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263512	F	MP:0002757	decreased vertical activity	Slc5a5<tm1b(KOMP)Wtsi>/Slc5a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc5a5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263512	F	MP:0002968	increased circulating alkaline phosphatase level	Slc5a5<tm1b(KOMP)Wtsi>/Slc5a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc5a5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263512	M	MP:0001488	increased startle reflex	Slc5a5<tm1b(KOMP)Wtsi>/Slc5a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc5a5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263512	F	MP:0005544	cornea deposits	Slc5a5<tm1b(KOMP)Wtsi>/Slc5a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc5a5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263512	F	MP:0001510	abnormal coat appearance	Slc5a5<tm1b(KOMP)Wtsi>/Slc5a5<tm1b(KOMP)Wtsi>	C57BL/6N-Slc5a5<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263514	F	MP:0002764	short tibia	Slc7a8<tm2b(EUCOMM)Hmgu>/Slc7a8<+>	C57BL/6N-Slc7a8<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263514	F	MP:0010088	decreased circulating fructosamine level	Slc7a8<tm2b(EUCOMM)Hmgu>/Slc7a8<+>	C57BL/6N-Slc7a8<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263515	F	MP:0010052	increased grip strength	Slc9a9<em1(IMPC)J>/Slc9a9<em1(IMPC)J>	C57BL/6NJ-Slc9a9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263515	M	MP:0001556	increased circulating HDL cholesterol level	Slc9a9<em1(IMPC)J>/Slc9a9<em1(IMPC)J>	C57BL/6NJ-Slc9a9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263516	M	MP:0001566	increased circulating phosphate level	Slc9b2<tm1.1(KOMP)Vlcg>/Slc9b2<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc9b2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263517	M	MP:0011496	abnormal head size	Slmap<em1(IMPC)J>/Slmap<em1(IMPC)J>	C57BL/6NJ-Slmap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263518	F	MP:0001399	hyperactivity	Smarcad1<tm1b(EUCOMM)Hmgu>/Smarcad1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Smarcad1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263518	M	MP:0001697	abnormal embryo size	Smarcad1<tm1b(EUCOMM)Hmgu>/Smarcad1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Smarcad1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263523	F	MP:0002965	increased circulating serum albumin level	Smc6<tm1b(EUCOMM)Hmgu>/Smc6<+>	C57BL/6N-Smc6<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263523	F	MP:0010024	increased total body fat amount	Smc6<tm1b(EUCOMM)Hmgu>/Smc6<+>	C57BL/6N-Smc6<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263525	F	MP:0001402	decreased locomotor activity	Smdt1<tm1b(EUCOMM)Wtsi>/Smdt1<+>	C57BL/6N-Smdt1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263525	M	MP:0000745	tremors	Smdt1<tm1b(EUCOMM)Wtsi>/Smdt1<+>	C57BL/6N-Smdt1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263526	F	MP:0005344	increased circulating bilirubin level	Smg1<tm1b(EUCOMM)Hmgu>/Smg1<+>	C57BL/6N-Smg1<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263530	F	MP:0001192	scaly skin	Smg6<em1(IMPC)Mbp>/Smg6<+>	C57BL/6NCrl-Smg6<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263530	F	MP:0000689	abnormal spleen morphology	Smg6<em1(IMPC)Mbp>/Smg6<+>	C57BL/6NCrl-Smg6<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263530	M	MP:0001486	abnormal startle reflex	Smg6<em1(IMPC)Mbp>/Smg6<+>	C57BL/6NCrl-Smg6<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263530	F	MP:0000691	enlarged spleen	Smg6<em1(IMPC)Mbp>/Smg6<+>	C57BL/6NCrl-Smg6<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263530	F	MP:0002060	abnormal skin morphology	Smg6<em1(IMPC)Mbp>/Smg6<+>	C57BL/6NCrl-Smg6<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263531	M	MP:0020870	decreased thigmotaxis	Smg9<em1(IMPC)J>/Smg9<+>	C57BL/6NJ-Smg9<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263531	M	MP:0004924	abnormal behavior	Smg9<em1(IMPC)J>/Smg9<+>	C57BL/6NJ-Smg9<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263531	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Smg9<em1(IMPC)J>/Smg9<+>	C57BL/6NJ-Smg9<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263531	M	MP:0001399	hyperactivity	Smg9<em1(IMPC)J>/Smg9<+>	C57BL/6NJ-Smg9<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263534	M	MP:0002060	abnormal skin morphology	Smpdl3a<em1(IMPC)Tcp>/Smpdl3a<em1(IMPC)Tcp>	C57BL/6NCrl-Smpdl3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263534	M	MP:0010506	prolonged RR interval	Smpdl3a<em1(IMPC)Tcp>/Smpdl3a<em1(IMPC)Tcp>	C57BL/6NCrl-Smpdl3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263535	M	MP:0001925	male infertility	Sms<tm1a(EUCOMM)Wtsi>/Sms<tm1a(EUCOMM)Wtsi>	B6JTyr;B6N-Sms<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263536	M	MP:0001488	increased startle reflex	Snap23<tm1b(EUCOMM)Wtsi>/Snap23<+>	C57BL/6N-Snap23<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263536	M	MP:0002075	abnormal coat/hair pigmentation	Snap23<tm1b(EUCOMM)Wtsi>/Snap23<+>	C57BL/6N-Snap23<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263539	F	MP:0001406	abnormal gait	Snapc1<tm1b(KOMP)Mbp>/Snapc1<+>	C57BL/6N-Snapc1<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6263539	F	MP:0005627	increased circulating potassium level	Snapc1<tm1b(KOMP)Mbp>/Snapc1<+>	C57BL/6N-Snapc1<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6263544	F	MP:0008806	increased circulating amylase level	Snca<em1(IMPC)H>/Snca<em1(IMPC)H>	C57BL/6NTac-Snca<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263544	M	MP:0005553	increased circulating creatinine level	Snca<em1(IMPC)H>/Snca<em1(IMPC)H>	C57BL/6NTac-Snca<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263544	F	MP:0001392	abnormal locomotor behavior	Snca<em1(IMPC)H>/Snca<em1(IMPC)H>	C57BL/6NTac-Snca<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263544	M	MP:0004952	increased spleen weight	Snca<em1(IMPC)H>/Snca<em1(IMPC)H>	C57BL/6NTac-Snca<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263544	F	MP:0013279	increased fasting circulating glucose level	Snca<em1(IMPC)H>/Snca<em1(IMPC)H>	C57BL/6NTac-Snca<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263545	M	MP:0000157	abnormal sternum morphology	Snd1<em1(IMPC)Tcp>/Snd1<em1(IMPC)Tcp>	C57BL/6NCrl-Snd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263551	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Snx8<tm2a(EUCOMM)Hmgu>/Snx8<tm2a(EUCOMM)Hmgu>	C57BL/6N-Snx8<tm2a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263551	M	MP:0000182	increased circulating LDL cholesterol level	Snx8<tm2a(EUCOMM)Hmgu>/Snx8<tm2a(EUCOMM)Hmgu>	C57BL/6N-Snx8<tm2a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263551	F	MP:0002966	decreased circulating alkaline phosphatase level	Snx8<tm2a(EUCOMM)Hmgu>/Snx8<tm2a(EUCOMM)Hmgu>	C57BL/6N-Snx8<tm2a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263551	F	MP:0005567	decreased circulating total protein level	Snx8<tm2a(EUCOMM)Hmgu>/Snx8<tm2a(EUCOMM)Hmgu>	C57BL/6N-Snx8<tm2a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263552	M	MP:0002997	enlarged seminal vesicle	Sorl1<tm1b(EUCOMM)Wtsi>/Sorl1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sorl1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263552	F	MP:0001325	abnormal retina morphology	Sorl1<tm1b(EUCOMM)Wtsi>/Sorl1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sorl1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263552	M	MP:0000443	abnormal snout morphology	Sorl1<tm1b(EUCOMM)Wtsi>/Sorl1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sorl1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263553	M	MP:0001925	male infertility	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	C57BL/6N-Spag17<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263554	F	MP:0011239	abnormal skin coloration	Spata31d1c<tm2b(EUCOMM)Hmgu>/Spata31d1c<tm2b(EUCOMM)Hmgu>	C57BL/6N-Spata31d1c<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263556	M	MP:0001925	male infertility	Spatc1l<em1(IMPC)H>/Spatc1l<em1(IMPC)H>	C57BL/6N-Spatc1l<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263556	F	MP:0005554	decreased circulating creatinine level	Spatc1l<em1(IMPC)H>/Spatc1l<em1(IMPC)H>	C57BL/6N-Spatc1l<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263557	F	MP:0009709	hydrometra	Speer4f1<em1(IMPC)Mbp>/Speer4f1<+>	C57BL/6NCrl-Speer4f1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263557	M	MP:0010024	increased total body fat amount	Speer4f1<em1(IMPC)Mbp>/Speer4f1<+>	C57BL/6NCrl-Speer4f1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263557	F	MP:0001120	abnormal uterus morphology	Speer4f1<em1(IMPC)Mbp>/Speer4f1<+>	C57BL/6NCrl-Speer4f1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263558	F	MP:0002968	increased circulating alkaline phosphatase level	Spin1<tm1.1(KOMP)Vlcg>/Spin1<+>	C57BL/6N-Spin1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263558	F	MP:0008259	abnormal optic disk morphology	Spin1<tm1.1(KOMP)Vlcg>/Spin1<+>	C57BL/6N-Spin1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263558	M	MP:0001488	increased startle reflex	Spin1<tm1.1(KOMP)Vlcg>/Spin1<+>	C57BL/6N-Spin1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263562	F	MP:0009142	decreased prepulse inhibition	Spock1<em1(IMPC)H>/Spock1<em1(IMPC)H>	C57BL/6N-Spock1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263562	F	MP:0010053	decreased grip strength	Spock1<em1(IMPC)H>/Spock1<em1(IMPC)H>	C57BL/6N-Spock1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263562	M	MP:0013278	decreased fasting circulating glucose level	Spock1<em1(IMPC)H>/Spock1<em1(IMPC)H>	C57BL/6N-Spock1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263563	F	MP:0001297	microphthalmia	Spred3<em1(IMPC)Tcp>/Spred3<+>	C57BL/6NCrl-Spred3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263563	F	MP:0005553	increased circulating creatinine level	Spred3<em1(IMPC)Tcp>/Spred3<+>	C57BL/6NCrl-Spred3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263563	F	MP:0004832	enlarged ovary	Spred3<em1(IMPC)Tcp>/Spred3<+>	C57BL/6NCrl-Spred3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263563	F	MP:0002989	small kidney	Spred3<em1(IMPC)Tcp>/Spred3<+>	C57BL/6NCrl-Spred3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263563	M	MP:0000702	enlarged lymph nodes	Spred3<em1(IMPC)Tcp>/Spred3<+>	C57BL/6NCrl-Spred3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263564	M	MP:0020421	increased freezing behavior	Spred3<em1(IMPC)Tcp>/Spred3<em1(IMPC)Tcp>	C57BL/6NCrl-Spred3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263565	M	MP:0001486	abnormal startle reflex	Sprr1a<em1(IMPC)J>/Sprr1a<em1(IMPC)J>	C57BL/6NJ-Sprr1a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263565	F	MP:0001314	cornea opacity	Sprr1a<em1(IMPC)J>/Sprr1a<em1(IMPC)J>	C57BL/6NJ-Sprr1a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263565	M	MP:0010053	decreased grip strength	Sprr1a<em1(IMPC)J>/Sprr1a<em1(IMPC)J>	C57BL/6NJ-Sprr1a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263565	F	MP:0001399	hyperactivity	Sprr1a<em1(IMPC)J>/Sprr1a<em1(IMPC)J>	C57BL/6NJ-Sprr1a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263566	M	MP:0005178	increased circulating cholesterol level	Spryd3<tm1b(EUCOMM)Hmgu>/Spryd3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spryd3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263566	M	MP:0002699	abnormal vitreous body morphology	Spryd3<tm1b(EUCOMM)Hmgu>/Spryd3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spryd3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263566	F	MP:0001488	increased startle reflex	Spryd3<tm1b(EUCOMM)Hmgu>/Spryd3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spryd3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263566	M	MP:0002079	increased circulating insulin level	Spryd3<tm1b(EUCOMM)Hmgu>/Spryd3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spryd3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263566	M	MP:0001556	increased circulating HDL cholesterol level	Spryd3<tm1b(EUCOMM)Hmgu>/Spryd3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Spryd3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263568	M	MP:0002059	abnormal seminal vesicle morphology	Spx<em1(IMPC)Tcp>/Spx<em1(IMPC)Tcp>	C57BL/6NCrl-Spx<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263571	F	MP:0010053	decreased grip strength	Srpk3<tm1b(KOMP)Wtsi>/Srpk3<tm1b(KOMP)Wtsi>	C57BL/6N-Srpk3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263572	M	MP:0002591	decreased mean corpuscular volume	Srprb<tm2b(EUCOMM)Hmgu>/Srprb<+>	C57BL/6N-Srprb<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263576	F	MP:0003179	thrombocytopenia	Srsf9<em1(IMPC)J>/Srsf9<+>	C57BL/6NJ-Srsf9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263577	F	MP:0010053	decreased grip strength	Ssh1<em1(IMPC)J>/Ssh1<em1(IMPC)J>	C57BL/6NJ-Ssh1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263581	M	MP:0001510	abnormal coat appearance	St6galnac3<em1(IMPC)J>/St6galnac3<em1(IMPC)J>	C57BL/6NJ-St6galnac3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263581	F	MP:0002098	abnormal vibrissa morphology	St6galnac3<em1(IMPC)J>/St6galnac3<em1(IMPC)J>	C57BL/6NJ-St6galnac3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263581	F	MP:0001304	cataract	St6galnac3<em1(IMPC)J>/St6galnac3<em1(IMPC)J>	C57BL/6NJ-St6galnac3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263582	F	MP:0001488	increased startle reflex	Stambp<tm1b(EUCOMM)Hmgu>/Stambp<+>	C57BL/6N-Stambp<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263582	M	MP:0003900	shortened QT interval	Stambp<tm1b(EUCOMM)Hmgu>/Stambp<+>	C57BL/6N-Stambp<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263584	M	MP:0010024	increased total body fat amount	Stau2<tm1a(EUCOMM)Wtsi>/Stau2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Stau2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263584	M	MP:0003961	decreased lean body mass	Stau2<tm1a(EUCOMM)Wtsi>/Stau2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Stau2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263585	F	MP:0003795	abnormal bone structure	Steap2<tm1b(EUCOMM)Hmgu>/Steap2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Steap2<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263586	F	MP:0001399	hyperactivity	Steap3<tm1b(EUCOMM)Hmgu>/Steap3<+>	C57BL/6N-Steap3<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263586	F	MP:0000208	decreased hematocrit	Steap3<tm1b(EUCOMM)Hmgu>/Steap3<+>	C57BL/6N-Steap3<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263586	F	MP:0002874	decreased hemoglobin content	Steap3<tm1b(EUCOMM)Hmgu>/Steap3<+>	C57BL/6N-Steap3<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263587	M	MP:0002591	decreased mean corpuscular volume	Steap3<tm1b(EUCOMM)Hmgu>/Steap3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Steap3<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263587	F	MP:0001399	hyperactivity	Steap3<tm1b(EUCOMM)Hmgu>/Steap3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Steap3<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263587	M	MP:0005293	impaired glucose tolerance	Steap3<tm1b(EUCOMM)Hmgu>/Steap3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Steap3<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263588	M	MP:0003960	increased lean body mass	Stim2<tm1.1(KOMP)Vlcg>/Stim2<+>	C57BL/6N-Stim2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263588	F	MP:0001488	increased startle reflex	Stim2<tm1.1(KOMP)Vlcg>/Stim2<+>	C57BL/6N-Stim2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263588	F	MP:0006243	impaired pupillary reflex	Stim2<tm1.1(KOMP)Vlcg>/Stim2<+>	C57BL/6N-Stim2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263588	M	MP:0001399	hyperactivity	Stim2<tm1.1(KOMP)Vlcg>/Stim2<+>	C57BL/6N-Stim2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263590	M	MP:0004486	decreased response of heart to induced stress	Stk11ip<em1(IMPC)J>/Stk11ip<em1(IMPC)J>	C57BL/6NJ-Stk11ip<em1(IMPC)J>/J	N	33486894
MGI:6263592	M	MP:0005566	decreased blood urea nitrogen level	Stk32c<tm2b(KOMP)Wtsi>/Stk32c<tm2b(KOMP)Wtsi>	C57BL/6N-Stk32c<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263592	M	MP:0010025	decreased total body fat amount	Stk32c<tm2b(KOMP)Wtsi>/Stk32c<tm2b(KOMP)Wtsi>	C57BL/6N-Stk32c<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263593	F	MP:0013279	increased fasting circulating glucose level	Stk38<tm1b(KOMP)Wtsi>/Stk38<+>	C57BL/6N-Stk38<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263593	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Stk38<tm1b(KOMP)Wtsi>/Stk38<+>	C57BL/6N-Stk38<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263593	F	MP:0002833	increased heart weight	Stk38<tm1b(KOMP)Wtsi>/Stk38<+>	C57BL/6N-Stk38<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263595	M	MP:0005343	increased circulating aspartate transaminase level	Stk3<em1(IMPC)H>/Stk3<em1(IMPC)H>	C57BL/6NTac-Stk3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263595	M	MP:0005553	increased circulating creatinine level	Stk3<em1(IMPC)H>/Stk3<em1(IMPC)H>	C57BL/6NTac-Stk3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263595	M	MP:0002941	increased circulating alanine transaminase level	Stk3<em1(IMPC)H>/Stk3<em1(IMPC)H>	C57BL/6NTac-Stk3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263595	M	MP:0000745	tremors	Stk3<em1(IMPC)H>/Stk3<em1(IMPC)H>	C57BL/6NTac-Stk3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263595	M	MP:0001406	abnormal gait	Stk3<em1(IMPC)H>/Stk3<em1(IMPC)H>	C57BL/6NTac-Stk3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263596	F	MP:0005292	improved glucose tolerance	Stmn4<tm1b(KOMP)Wtsi>/Stmn4<tm1b(KOMP)Wtsi>	C57BL/6N-Stmn4<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263597	F	MP:0001325	abnormal retina morphology	Stox2<tm2b(EUCOMM)Hmgu>/Stox2<+>	C57BL/6N-Stox2<tm2b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263597	M	MP:0002833	increased heart weight	Stox2<tm2b(EUCOMM)Hmgu>/Stox2<+>	C57BL/6N-Stox2<tm2b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263597	F	MP:0013278	decreased fasting circulating glucose level	Stox2<tm2b(EUCOMM)Hmgu>/Stox2<+>	C57BL/6N-Stox2<tm2b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263597	F	MP:0005562	decreased mean corpuscular hemoglobin	Stox2<tm2b(EUCOMM)Hmgu>/Stox2<+>	C57BL/6N-Stox2<tm2b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263599	F	MP:0002591	decreased mean corpuscular volume	Stradb<tm1b(KOMP)Wtsi>/Stradb<tm1b(KOMP)Wtsi>	C57BL/6N-Stradb<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6263600	M	MP:0001304	cataract	Stx2<tm1b(EUCOMM)Wtsi>/Stx2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Stx2<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263600	M	MP:0001925	male infertility	Stx2<tm1b(EUCOMM)Wtsi>/Stx2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Stx2<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263600	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Stx2<tm1b(EUCOMM)Wtsi>/Stx2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Stx2<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263600	M	MP:0005178	increased circulating cholesterol level	Stx2<tm1b(EUCOMM)Wtsi>/Stx2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Stx2<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263600	M	MP:0003131	increased erythrocyte cell number	Stx2<tm1b(EUCOMM)Wtsi>/Stx2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Stx2<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6263601	M	MP:0002699	abnormal vitreous body morphology	Stx5a<tm1b(EUCOMM)Hmgu>/Stx5a<+>	C57BL/6N-Stx5a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263601	M	MP:0011965	decreased total retina thickness	Stx5a<tm1b(EUCOMM)Hmgu>/Stx5a<+>	C57BL/6N-Stx5a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263601	M	MP:0010067	increased red blood cell distribution width	Stx5a<tm1b(EUCOMM)Hmgu>/Stx5a<+>	C57BL/6N-Stx5a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263601	M	MP:0002792	abnormal retina vasculature morphology	Stx5a<tm1b(EUCOMM)Hmgu>/Stx5a<+>	C57BL/6N-Stx5a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263601	M	MP:0010097	abnormal retina blood vessel morphology	Stx5a<tm1b(EUCOMM)Hmgu>/Stx5a<+>	C57BL/6N-Stx5a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263604	F	MP:0002590	increased mean corpuscular volume	Stxbp1<tm1b(EUCOMM)Hmgu>/Stxbp1<+>	C57BL/6N-Stxbp1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263604	M	MP:0000208	decreased hematocrit	Stxbp1<tm1b(EUCOMM)Hmgu>/Stxbp1<+>	C57BL/6N-Stxbp1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263604	F	MP:0005293	impaired glucose tolerance	Stxbp1<tm1b(EUCOMM)Hmgu>/Stxbp1<+>	C57BL/6N-Stxbp1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263604	M	MP:0010052	increased grip strength	Stxbp1<tm1b(EUCOMM)Hmgu>/Stxbp1<+>	C57BL/6N-Stxbp1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263604	F	MP:0001415	increased exploration in new environment	Stxbp1<tm1b(EUCOMM)Hmgu>/Stxbp1<+>	C57BL/6N-Stxbp1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263606	M	MP:0001925	male infertility	Styxl1<em1(IMPC)J>/Styxl1<em1(IMPC)J>	C57BL/6NJ-Styxl1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263607	F	MP:0002339	abnormal lymph node morphology	Sugp1<em1(IMPC)Mbp>/Sugp1<+>	C57BL/6NCrl-Sugp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263607	F	MP:0000702	enlarged lymph nodes	Sugp1<em1(IMPC)Mbp>/Sugp1<+>	C57BL/6NCrl-Sugp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263607	F	MP:0000601	small liver	Sugp1<em1(IMPC)Mbp>/Sugp1<+>	C57BL/6NCrl-Sugp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263607	F	MP:0001126	abnormal ovary morphology	Sugp1<em1(IMPC)Mbp>/Sugp1<+>	C57BL/6NCrl-Sugp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263607	F	MP:0003984	embryonic growth retardation	Sugp1<em1(IMPC)Mbp>/Sugp1<+>	C57BL/6NCrl-Sugp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263607	F	MP:0020420	abnormal freezing behavior	Sugp1<em1(IMPC)Mbp>/Sugp1<+>	C57BL/6NCrl-Sugp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263607	F	MP:0001120	abnormal uterus morphology	Sugp1<em1(IMPC)Mbp>/Sugp1<+>	C57BL/6NCrl-Sugp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263609	M	MP:0000266	abnormal heart morphology	Sumf1<tm1b(KOMP)Wtsi>/Sumf1<+>	C57BL/6N-Sumf1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263609	M	MP:0000274	enlarged heart	Sumf1<tm1b(KOMP)Wtsi>/Sumf1<+>	C57BL/6N-Sumf1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263610	M	MP:0000266	abnormal heart morphology	Sumo1<tm1.1(KOMP)Vlcg>/Sumo1<+>	C57BL/6N-Sumo1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263610	M	MP:0000274	enlarged heart	Sumo1<tm1.1(KOMP)Vlcg>/Sumo1<+>	C57BL/6N-Sumo1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263611	M	MP:0005567	decreased circulating total protein level	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	F	MP:0000218	increased leukocyte cell number	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	M	MP:0001489	decreased startle reflex	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	F	MP:0001926	female infertility	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	M	MP:0005419	decreased circulating serum albumin level	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	F	MP:0001402	decreased locomotor activity	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	M	MP:0001486	abnormal startle reflex	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	F	MP:0003961	decreased lean body mass	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	M	MP:0000219	increased neutrophil cell number	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	F	MP:0001102	small superior vagus ganglion	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	M	MP:0005016	decreased lymphocyte cell number	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	M	MP:0001925	male infertility	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	M	MP:0002626	increased heart rate	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	F	MP:0005013	increased lymphocyte cell number	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	F	MP:0003731	abnormal retina outer nuclear layer morphology	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	F	MP:0010024	increased total body fat amount	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	M	MP:0001147	small testis	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263611	M	MP:0001566	increased circulating phosphate level	Sun1<tm1b(EUCOMM)Wtsi>/Sun1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Sun1<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6263612	F	MP:0003961	decreased lean body mass	Sun2<tm1b(EUCOMM)Hmgu>/Sun2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sun2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263612	M	MP:0012362	increased large unstained cell number	Sun2<tm1b(EUCOMM)Hmgu>/Sun2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sun2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263612	F	MP:0003795	abnormal bone structure	Sun2<tm1b(EUCOMM)Hmgu>/Sun2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sun2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263615	F	MP:0008806	increased circulating amylase level	Susd6<tm1b(KOMP)Wtsi>/Susd6<tm1b(KOMP)Wtsi>	C57BL/6N-Susd6<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263615	M	MP:0003179	thrombocytopenia	Susd6<tm1b(KOMP)Wtsi>/Susd6<tm1b(KOMP)Wtsi>	C57BL/6N-Susd6<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263615	M	MP:0002941	increased circulating alanine transaminase level	Susd6<tm1b(KOMP)Wtsi>/Susd6<tm1b(KOMP)Wtsi>	C57BL/6N-Susd6<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263615	M	MP:0000691	enlarged spleen	Susd6<tm1b(KOMP)Wtsi>/Susd6<tm1b(KOMP)Wtsi>	C57BL/6N-Susd6<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263615	M	MP:0001488	increased startle reflex	Susd6<tm1b(KOMP)Wtsi>/Susd6<tm1b(KOMP)Wtsi>	C57BL/6N-Susd6<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263615	F	MP:0005344	increased circulating bilirubin level	Susd6<tm1b(KOMP)Wtsi>/Susd6<tm1b(KOMP)Wtsi>	C57BL/6N-Susd6<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263615	M	MP:0005343	increased circulating aspartate transaminase level	Susd6<tm1b(KOMP)Wtsi>/Susd6<tm1b(KOMP)Wtsi>	C57BL/6N-Susd6<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263615	M	MP:0010025	decreased total body fat amount	Susd6<tm1b(KOMP)Wtsi>/Susd6<tm1b(KOMP)Wtsi>	C57BL/6N-Susd6<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263615	M	MP:0000222	decreased neutrophil cell number	Susd6<tm1b(KOMP)Wtsi>/Susd6<tm1b(KOMP)Wtsi>	C57BL/6N-Susd6<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263616	F	MP:0005561	increased mean corpuscular hemoglobin	Svop<em1(IMPC)H>/Svop<em1(IMPC)H>	C57BL/6N-Svop<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263616	F	MP:0001406	abnormal gait	Svop<em1(IMPC)H>/Svop<em1(IMPC)H>	C57BL/6N-Svop<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263616	F	MP:0001523	impaired righting response	Svop<em1(IMPC)H>/Svop<em1(IMPC)H>	C57BL/6N-Svop<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263616	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Svop<em1(IMPC)H>/Svop<em1(IMPC)H>	C57BL/6N-Svop<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263618	F	MP:0001513	limb grasping	Syce1<tm1b(KOMP)Wtsi>/Syce1<tm1b(KOMP)Wtsi>	C57BL/6N-Syce1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263618	F	MP:0010053	decreased grip strength	Syce1<tm1b(KOMP)Wtsi>/Syce1<tm1b(KOMP)Wtsi>	C57BL/6N-Syce1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263618	F	MP:0010124	decreased bone mineral content	Syce1<tm1b(KOMP)Wtsi>/Syce1<tm1b(KOMP)Wtsi>	C57BL/6N-Syce1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263618	F	MP:0001926	female infertility	Syce1<tm1b(KOMP)Wtsi>/Syce1<tm1b(KOMP)Wtsi>	C57BL/6N-Syce1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263618	M	MP:0001925	male infertility	Syce1<tm1b(KOMP)Wtsi>/Syce1<tm1b(KOMP)Wtsi>	C57BL/6N-Syce1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263618	F	MP:0002797	increased thigmotaxis	Syce1<tm1b(KOMP)Wtsi>/Syce1<tm1b(KOMP)Wtsi>	C57BL/6N-Syce1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263618	F	MP:0001402	decreased locomotor activity	Syce1<tm1b(KOMP)Wtsi>/Syce1<tm1b(KOMP)Wtsi>	C57BL/6N-Syce1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263618	M	MP:0002959	increased urine microalbumin level	Syce1<tm1b(KOMP)Wtsi>/Syce1<tm1b(KOMP)Wtsi>	C57BL/6N-Syce1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263618	F	MP:0000063	decreased bone mineral density	Syce1<tm1b(KOMP)Wtsi>/Syce1<tm1b(KOMP)Wtsi>	C57BL/6N-Syce1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263619	M	MP:0001417	decreased exploration in new environment	Syk<tm1b(EUCOMM)Hmgu>/Syk<+>	C57BL/6N-Syk<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263623	F	MP:0005565	increased blood urea nitrogen level	Syt17<tm1b(KOMP)Wtsi>/Syt17<tm1b(KOMP)Wtsi>	C57BL/6N-Syt17<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263623	M	MP:0002764	short tibia	Syt17<tm1b(KOMP)Wtsi>/Syt17<tm1b(KOMP)Wtsi>	C57BL/6N-Syt17<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263624	F	MP:0000198	decreased circulating phosphate level	Syt7<em2(IMPC)H>/Syt7<em2(IMPC)H>	C57BL/6N-Syt7<em2(IMPC)H>/H	N	MGI:5576271
MGI:6263628	M	MP:0010052	increased grip strength	Taf13<em1(IMPC)J>/Taf13<+>	C57BL/6NJ-Taf13<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263630	M	MP:0004357	long tibia	Taf2<tm1b(EUCOMM)Hmgu>/Taf2<+>	C57BL/6N-Taf2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6263632	F	MP:0000266	abnormal heart morphology	Taf9b<tm1.1(KOMP)Vlcg>/Taf9b<tm1.1(KOMP)Vlcg>	C57BL/6N-Taf9b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263632	F	MP:0000274	enlarged heart	Taf9b<tm1.1(KOMP)Vlcg>/Taf9b<tm1.1(KOMP)Vlcg>	C57BL/6N-Taf9b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263633	M	MP:0011874	enlarged urinary bladder	Tanc1<em1(IMPC)Tcp>/Tanc1<em1(IMPC)Tcp>	C57BL/6NCrl-Tanc1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263633	M	MP:0005343	increased circulating aspartate transaminase level	Tanc1<em1(IMPC)Tcp>/Tanc1<em1(IMPC)Tcp>	C57BL/6NCrl-Tanc1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263633	F	MP:0002060	abnormal skin morphology	Tanc1<em1(IMPC)Tcp>/Tanc1<em1(IMPC)Tcp>	C57BL/6NCrl-Tanc1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263636	M	MP:0011110	preweaning lethality, incomplete penetrance	Tarbp1<tm1b(EUCOMM)Hmgu>/Tarbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tarbp1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263636	F	MP:0011239	abnormal skin coloration	Tarbp1<tm1b(EUCOMM)Hmgu>/Tarbp1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tarbp1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263637	M	MP:0001146	abnormal testis morphology	Tas2r139<em1(IMPC)Mbp>/Tas2r139<em1(IMPC)Mbp>	C57BL/6NCrl-Tas2r139<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263637	M	MP:0002059	abnormal seminal vesicle morphology	Tas2r139<em1(IMPC)Mbp>/Tas2r139<em1(IMPC)Mbp>	C57BL/6NCrl-Tas2r139<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263637	M	MP:0001147	small testis	Tas2r139<em1(IMPC)Mbp>/Tas2r139<em1(IMPC)Mbp>	C57BL/6NCrl-Tas2r139<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263637	F	MP:0000689	abnormal spleen morphology	Tas2r139<em1(IMPC)Mbp>/Tas2r139<em1(IMPC)Mbp>	C57BL/6NCrl-Tas2r139<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263637	F	MP:0000692	small spleen	Tas2r139<em1(IMPC)Mbp>/Tas2r139<em1(IMPC)Mbp>	C57BL/6NCrl-Tas2r139<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263639	M	MP:0003960	increased lean body mass	Tat<em1(IMPC)J>/Tat<em1(IMPC)J>	C57BL/6NJ-Tat<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263639	M	MP:0010025	decreased total body fat amount	Tat<em1(IMPC)J>/Tat<em1(IMPC)J>	C57BL/6NJ-Tat<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263639	M	MP:0005333	decreased heart rate	Tat<em1(IMPC)J>/Tat<em1(IMPC)J>	C57BL/6NJ-Tat<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263639	M	MP:0010052	increased grip strength	Tat<em1(IMPC)J>/Tat<em1(IMPC)J>	C57BL/6NJ-Tat<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263639	M	MP:0001510	abnormal coat appearance	Tat<em1(IMPC)J>/Tat<em1(IMPC)J>	C57BL/6NJ-Tat<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263639	M	MP:0002075	abnormal coat/hair pigmentation	Tat<em1(IMPC)J>/Tat<em1(IMPC)J>	C57BL/6NJ-Tat<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263639	M	MP:0001325	abnormal retina morphology	Tat<em1(IMPC)J>/Tat<em1(IMPC)J>	C57BL/6NJ-Tat<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263639	F	MP:0005561	increased mean corpuscular hemoglobin	Tat<em1(IMPC)J>/Tat<em1(IMPC)J>	C57BL/6NJ-Tat<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263641	M	MP:0010124	decreased bone mineral content	Tbc1d16<em1(IMPC)J>/Tbc1d16<em1(IMPC)J>	C57BL/6NJ-Tbc1d16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263641	M	MP:0000063	decreased bone mineral density	Tbc1d16<em1(IMPC)J>/Tbc1d16<em1(IMPC)J>	C57BL/6NJ-Tbc1d16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263641	F	MP:0002968	increased circulating alkaline phosphatase level	Tbc1d16<em1(IMPC)J>/Tbc1d16<em1(IMPC)J>	C57BL/6NJ-Tbc1d16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263642	F	MP:0000367	abnormal coat/ hair morphology	Tbc1d30<em1(IMPC)J>/Tbc1d30<em1(IMPC)J>	C57BL/6NJ-Tbc1d30<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263642	M	MP:0004924	abnormal behavior	Tbc1d30<em1(IMPC)J>/Tbc1d30<em1(IMPC)J>	C57BL/6NJ-Tbc1d30<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263642	M	MP:0020870	decreased thigmotaxis	Tbc1d30<em1(IMPC)J>/Tbc1d30<em1(IMPC)J>	C57BL/6NJ-Tbc1d30<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263643	M	MP:0005178	increased circulating cholesterol level	Tbc1d5<em1(IMPC)J>/Tbc1d5<em1(IMPC)J>	C57BL/6NJ-Tbc1d5<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263643	F	MP:0010053	decreased grip strength	Tbc1d5<em1(IMPC)J>/Tbc1d5<em1(IMPC)J>	C57BL/6NJ-Tbc1d5<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263643	F	MP:0001289	persistence of hyaloid vascular system	Tbc1d5<em1(IMPC)J>/Tbc1d5<em1(IMPC)J>	C57BL/6NJ-Tbc1d5<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263643	F	MP:0000572	abnormal autopod morphology	Tbc1d5<em1(IMPC)J>/Tbc1d5<em1(IMPC)J>	C57BL/6NJ-Tbc1d5<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263644	M	MP:0001925	male infertility	Tbc1d8<em1(IMPC)J>/Tbc1d8<em1(IMPC)J>	C57BL/6NJ-Tbc1d8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263644	F	MP:0001304	cataract	Tbc1d8<em1(IMPC)J>/Tbc1d8<em1(IMPC)J>	C57BL/6NJ-Tbc1d8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263645	M	MP:0001303	abnormal lens morphology	Tbce<tm2b(EUCOMM)Hmgu>/Tbce<+>	C57BL/6N-Tbce<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263645	M	MP:0001304	cataract	Tbce<tm2b(EUCOMM)Hmgu>/Tbce<+>	C57BL/6N-Tbce<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263650	M	MP:0002060	abnormal skin morphology	Tceal3<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Tceal3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263650	M	MP:0011874	enlarged urinary bladder	Tceal3<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Tceal3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263650	M	MP:0000702	enlarged lymph nodes	Tceal3<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Tceal3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263653	M	MP:0003984	embryonic growth retardation	Tcerg1<em1(IMPC)J>/Tcerg1<em1(IMPC)J>	C57BL/6NJ-Tcerg1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263654	M	MP:0013278	decreased fasting circulating glucose level	Tcerg1l<tm1a(KOMP)Wtsi>/Tcerg1l<tm1a(KOMP)Wtsi>	C57BL/6N-Tcerg1l<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263655	F	MP:0003961	decreased lean body mass	Tcf20<em1(IMPC)Wtsi>/Tcf20<em1(IMPC)Wtsi>	C57BL/6N-Tcf20<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263655	M	MP:0002968	increased circulating alkaline phosphatase level	Tcf20<em1(IMPC)Wtsi>/Tcf20<em1(IMPC)Wtsi>	C57BL/6N-Tcf20<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263655	F	MP:0005343	increased circulating aspartate transaminase level	Tcf20<em1(IMPC)Wtsi>/Tcf20<em1(IMPC)Wtsi>	C57BL/6N-Tcf20<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263655	F	MP:0010024	increased total body fat amount	Tcf20<em1(IMPC)Wtsi>/Tcf20<em1(IMPC)Wtsi>	C57BL/6N-Tcf20<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263655	M	MP:0002079	increased circulating insulin level	Tcf20<em1(IMPC)Wtsi>/Tcf20<em1(IMPC)Wtsi>	C57BL/6N-Tcf20<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263656	M	MP:0020421	increased freezing behavior	Tcf25<em1(IMPC)Mbp>/Tcf25<em1(IMPC)Mbp>	C57BL/6NCrl-Tcf25<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263656	M	MP:0001146	abnormal testis morphology	Tcf25<em1(IMPC)Mbp>/Tcf25<em1(IMPC)Mbp>	C57BL/6NCrl-Tcf25<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263656	M	MP:0002135	abnormal kidney morphology	Tcf25<em1(IMPC)Mbp>/Tcf25<em1(IMPC)Mbp>	C57BL/6NCrl-Tcf25<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263656	F	MP:0003179	thrombocytopenia	Tcf25<em1(IMPC)Mbp>/Tcf25<em1(IMPC)Mbp>	C57BL/6NCrl-Tcf25<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263656	M	MP:0001147	small testis	Tcf25<em1(IMPC)Mbp>/Tcf25<em1(IMPC)Mbp>	C57BL/6NCrl-Tcf25<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263656	M	MP:0003068	enlarged kidney	Tcf25<em1(IMPC)Mbp>/Tcf25<em1(IMPC)Mbp>	C57BL/6NCrl-Tcf25<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263658	M	MP:0001925	male infertility	Tcte1<tm1a(KOMP)Wtsi>/Tcte1<tm1a(KOMP)Wtsi>	C57BL/6N-Tcte1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263659	M	MP:0001925	male infertility	Dynlt2b<tm2b(EUCOMM)Wtsi>/Dynlt2b<tm2b(EUCOMM)Wtsi>	C57BL/6N-Dynlt2b<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263661	F	MP:0000195	decreased circulating calcium level	Tctn3<em1(IMPC)J>/Tctn3<+>	C57BL/6NJ-Tctn3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263661	F	MP:0005278	abnormal cholesterol homeostasis	Tctn3<em1(IMPC)J>/Tctn3<+>	C57BL/6NJ-Tctn3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263661	F	MP:0005567	decreased circulating total protein level	Tctn3<em1(IMPC)J>/Tctn3<+>	C57BL/6NJ-Tctn3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263662	F	MP:0001293	anophthalmia	Tctn3<em1(IMPC)J>/Tctn3<em1(IMPC)J>	C57BL/6NJ-Tctn3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263662	F	MP:0001697	abnormal embryo size	Tctn3<em1(IMPC)J>/Tctn3<em1(IMPC)J>	C57BL/6NJ-Tctn3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263662	F	MP:0003385	abnormal body wall morphology	Tctn3<em1(IMPC)J>/Tctn3<em1(IMPC)J>	C57BL/6NJ-Tctn3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263662	F	MP:0000562	polydactyly	Tctn3<em1(IMPC)J>/Tctn3<em1(IMPC)J>	C57BL/6NJ-Tctn3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263663	F	MP:0002574	increased vertical activity	Tecpr2<em1(IMPC)J>/Tecpr2<em1(IMPC)J>	C57BL/6NJ-Tecpr2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263663	F	MP:0001529	abnormal vocalization	Tecpr2<em1(IMPC)J>/Tecpr2<em1(IMPC)J>	C57BL/6NJ-Tecpr2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263665	M	MP:0005565	increased blood urea nitrogen level	Tedc1<em1(IMPC)Tcp>/Tedc1<+>	C57BL/6NCrl-Tedc1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263665	F	MP:0001120	abnormal uterus morphology	Tedc1<em1(IMPC)Tcp>/Tedc1<+>	C57BL/6NCrl-Tedc1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263669	M	MP:0005560	decreased circulating glucose level	Tex101<tm1b(KOMP)Wtsi>/Tex101<tm1b(KOMP)Wtsi>	C57BL/6N-Tex101<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263669	M	MP:0005633	increased circulating sodium level	Tex101<tm1b(KOMP)Wtsi>/Tex101<tm1b(KOMP)Wtsi>	C57BL/6N-Tex101<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263670	F	MP:0010506	prolonged RR interval	Tex2<em1(IMPC)J>/Tex2<em1(IMPC)J>	C57BL/6NJ-Tex2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263670	M	MP:0005554	decreased circulating creatinine level	Tex2<em1(IMPC)J>/Tex2<em1(IMPC)J>	C57BL/6NJ-Tex2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263670	F	MP:0005333	decreased heart rate	Tex2<em1(IMPC)J>/Tex2<em1(IMPC)J>	C57BL/6NJ-Tex2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263670	F	MP:0010053	decreased grip strength	Tex2<em1(IMPC)J>/Tex2<em1(IMPC)J>	C57BL/6NJ-Tex2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263671	M	MP:0010124	decreased bone mineral content	Tex38<tm1a(KOMP)Wtsi>/Tex38<tm1a(KOMP)Wtsi>	C57BL/6N-Tex38<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263671	M	MP:0001925	male infertility	Tex38<tm1a(KOMP)Wtsi>/Tex38<tm1a(KOMP)Wtsi>	C57BL/6N-Tex38<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263671	M	MP:0000063	decreased bone mineral density	Tex38<tm1a(KOMP)Wtsi>/Tex38<tm1a(KOMP)Wtsi>	C57BL/6N-Tex38<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263672	M	MP:0010052	increased grip strength	Tfap2b<tm1b(EUCOMM)Wtsi>/Tfap2b<+>	C57BL/6N-Tfap2b<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6263677	M	MP:0005630	increased lung weight	Thbd<tm1.1(KOMP)Vlcg>/Thbd<+>	C57BL/6N-Thbd<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263680	F	MP:0004832	enlarged ovary	Thoc6<em5(IMPC)Tcp>/Thoc6<+>	C57BL/6NCrl-Thoc6<em5(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263680	F	MP:0001175	abnormal lung morphology	Thoc6<em5(IMPC)Tcp>/Thoc6<+>	C57BL/6NCrl-Thoc6<em5(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263680	M	MP:0002757	decreased vertical activity	Thoc6<em5(IMPC)Tcp>/Thoc6<+>	C57BL/6NCrl-Thoc6<em5(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263680	M	MP:0000702	enlarged lymph nodes	Thoc6<em5(IMPC)Tcp>/Thoc6<+>	C57BL/6NCrl-Thoc6<em5(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263683	M	MP:0010124	decreased bone mineral content	Thsd7a<tm1b(KOMP)Mbp>/Thsd7a<tm1b(KOMP)Mbp>	C57BL/6N-Thsd7a<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263683	F	MP:0001304	cataract	Thsd7a<tm1b(KOMP)Mbp>/Thsd7a<tm1b(KOMP)Mbp>	C57BL/6N-Thsd7a<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263683	M	MP:0001325	abnormal retina morphology	Thsd7a<tm1b(KOMP)Mbp>/Thsd7a<tm1b(KOMP)Mbp>	C57BL/6N-Thsd7a<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263683	M	MP:0003961	decreased lean body mass	Thsd7a<tm1b(KOMP)Mbp>/Thsd7a<tm1b(KOMP)Mbp>	C57BL/6N-Thsd7a<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263684	M	MP:0005179	decreased circulating cholesterol level	Tial1<tm1b(EUCOMM)Wtsi>/Tial1<+>	C57BL/6N-Tial1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263684	M	MP:0010025	decreased total body fat amount	Tial1<tm1b(EUCOMM)Wtsi>/Tial1<+>	C57BL/6N-Tial1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263684	M	MP:0003960	increased lean body mass	Tial1<tm1b(EUCOMM)Wtsi>/Tial1<+>	C57BL/6N-Tial1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263684	M	MP:0005505	thrombocytosis	Tial1<tm1b(EUCOMM)Wtsi>/Tial1<+>	C57BL/6N-Tial1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263684	M	MP:0000186	decreased circulating HDL cholesterol level	Tial1<tm1b(EUCOMM)Wtsi>/Tial1<+>	C57BL/6N-Tial1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263684	M	MP:0000062	increased bone mineral density	Tial1<tm1b(EUCOMM)Wtsi>/Tial1<+>	C57BL/6N-Tial1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263684	M	MP:0000195	decreased circulating calcium level	Tial1<tm1b(EUCOMM)Wtsi>/Tial1<+>	C57BL/6N-Tial1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263685	M	MP:0011962	increased cornea thickness	Tiam1<tm1b(EUCOMM)Hmgu>/Tiam1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tiam1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6263685	F	MP:0001402	decreased locomotor activity	Tiam1<tm1b(EUCOMM)Hmgu>/Tiam1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tiam1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6263687	M	MP:0005565	increased blood urea nitrogen level	Timm8a1<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Timm8a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263687	M	MP:0002968	increased circulating alkaline phosphatase level	Timm8a1<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Timm8a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263687	M	MP:0005567	decreased circulating total protein level	Timm8a1<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Timm8a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263688	F	MP:0005344	increased circulating bilirubin level	Timm8a1<em1(IMPC)Tcp>/Timm8a1<em1(IMPC)Tcp>	C57BL/6NCrl-Timm8a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263688	F	MP:0002968	increased circulating alkaline phosphatase level	Timm8a1<em1(IMPC)Tcp>/Timm8a1<em1(IMPC)Tcp>	C57BL/6NCrl-Timm8a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263688	F	MP:0010067	increased red blood cell distribution width	Timm8a1<em1(IMPC)Tcp>/Timm8a1<em1(IMPC)Tcp>	C57BL/6NCrl-Timm8a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263690	F	MP:0009709	hydrometra	Tiparp<tm1b(EUCOMM)Wtsi>/Tiparp<+>	C57BL/6N-Tiparp<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263690	M	MP:0002060	abnormal skin morphology	Tiparp<tm1b(EUCOMM)Wtsi>/Tiparp<+>	C57BL/6N-Tiparp<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263690	M	MP:0000266	abnormal heart morphology	Tiparp<tm1b(EUCOMM)Wtsi>/Tiparp<+>	C57BL/6N-Tiparp<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263690	F	MP:0001102	small superior vagus ganglion	Tiparp<tm1b(EUCOMM)Wtsi>/Tiparp<+>	C57BL/6N-Tiparp<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263690	M	MP:0000274	enlarged heart	Tiparp<tm1b(EUCOMM)Wtsi>/Tiparp<+>	C57BL/6N-Tiparp<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263690	M	MP:0001192	scaly skin	Tiparp<tm1b(EUCOMM)Wtsi>/Tiparp<+>	C57BL/6N-Tiparp<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263691	F	MP:0000691	enlarged spleen	Tiparp<tm1b(EUCOMM)Wtsi>/Tiparp<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tiparp<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263691	F	MP:0000689	abnormal spleen morphology	Tiparp<tm1b(EUCOMM)Wtsi>/Tiparp<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tiparp<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263691	F	MP:0009709	hydrometra	Tiparp<tm1b(EUCOMM)Wtsi>/Tiparp<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tiparp<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263691	F	MP:0001102	small superior vagus ganglion	Tiparp<tm1b(EUCOMM)Wtsi>/Tiparp<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tiparp<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263692	M	MP:0003232	abnormal forebrain development	Tiprl<tm1.1(KOMP)Vlcg>/Tiprl<tm1.1(KOMP)Vlcg>	C57BL/6N-Tiprl<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263693	F	MP:0002060	abnormal skin morphology	Meak7<em3(IMPC)Tcp>/Meak7<em3(IMPC)Tcp>	C57BL/6NCrl-Meak7<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263693	F	MP:0001175	abnormal lung morphology	Meak7<em3(IMPC)Tcp>/Meak7<em3(IMPC)Tcp>	C57BL/6NCrl-Meak7<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263693	M	MP:0002631	abnormal epididymis morphology	Meak7<em3(IMPC)Tcp>/Meak7<em3(IMPC)Tcp>	C57BL/6NCrl-Meak7<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263694	F	MP:0005562	decreased mean corpuscular hemoglobin	Tlk1<tm1b(EUCOMM)Hmgu>/Tlk1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tlk1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263694	M	MP:0005344	increased circulating bilirubin level	Tlk1<tm1b(EUCOMM)Hmgu>/Tlk1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tlk1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263694	M	MP:0001566	increased circulating phosphate level	Tlk1<tm1b(EUCOMM)Hmgu>/Tlk1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tlk1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263694	M	MP:0003179	thrombocytopenia	Tlk1<tm1b(EUCOMM)Hmgu>/Tlk1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tlk1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263694	F	MP:0005293	impaired glucose tolerance	Tlk1<tm1b(EUCOMM)Hmgu>/Tlk1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tlk1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263694	F	MP:0002968	increased circulating alkaline phosphatase level	Tlk1<tm1b(EUCOMM)Hmgu>/Tlk1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tlk1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6263696	F	MP:0009476	enlarged cecum	Tlr4<tm1.1(KOMP)Vlcg>/Tlr4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tlr4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263696	F	MP:0004906	enlarged uterus	Tlr4<tm1.1(KOMP)Vlcg>/Tlr4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tlr4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263696	F	MP:0000494	abnormal cecum morphology	Tlr4<tm1.1(KOMP)Vlcg>/Tlr4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tlr4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263696	F	MP:0001120	abnormal uterus morphology	Tlr4<tm1.1(KOMP)Vlcg>/Tlr4<tm1.1(KOMP)Vlcg>	C57BL/6N-Tlr4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263697	M	MP:0001363	increased anxiety-related response	Tm2d3<em1(IMPC)J>/Tm2d3<+>	C57BL/6NJ-Tm2d3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263699	F	MP:0002092	abnormal eye morphology	Tmc7<em1(IMPC)Mbp>/Tmc7<em1(IMPC)Mbp>	C57BL/6NCrl-Tmc7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263699	M	MP:0005178	increased circulating cholesterol level	Tmc7<em1(IMPC)Mbp>/Tmc7<em1(IMPC)Mbp>	C57BL/6NCrl-Tmc7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263699	F	MP:0001926	female infertility	Tmc7<em1(IMPC)Mbp>/Tmc7<em1(IMPC)Mbp>	C57BL/6NCrl-Tmc7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263699	F	MP:0002060	abnormal skin morphology	Tmc7<em1(IMPC)Mbp>/Tmc7<em1(IMPC)Mbp>	C57BL/6NCrl-Tmc7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263699	M	MP:0001925	male infertility	Tmc7<em1(IMPC)Mbp>/Tmc7<em1(IMPC)Mbp>	C57BL/6NCrl-Tmc7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263699	F	MP:0001126	abnormal ovary morphology	Tmc7<em1(IMPC)Mbp>/Tmc7<em1(IMPC)Mbp>	C57BL/6NCrl-Tmc7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263699	F	MP:0001297	microphthalmia	Tmc7<em1(IMPC)Mbp>/Tmc7<em1(IMPC)Mbp>	C57BL/6NCrl-Tmc7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263699	M	MP:0000598	abnormal liver morphology	Tmc7<em1(IMPC)Mbp>/Tmc7<em1(IMPC)Mbp>	C57BL/6NCrl-Tmc7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263699	F	MP:0000691	enlarged spleen	Tmc7<em1(IMPC)Mbp>/Tmc7<em1(IMPC)Mbp>	C57BL/6NCrl-Tmc7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263699	F	MP:0000689	abnormal spleen morphology	Tmc7<em1(IMPC)Mbp>/Tmc7<em1(IMPC)Mbp>	C57BL/6NCrl-Tmc7<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263700	F	MP:0001926	female infertility	Tmco1<em1(IMPC)J>/Tmco1<em1(IMPC)J>	C57BL/6NJ-Tmco1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263701	F	MP:0010124	decreased bone mineral content	Tmco6<tm1.1(KOMP)Vlcg>/Tmco6<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmco6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263701	M	MP:0000195	decreased circulating calcium level	Tmco6<tm1.1(KOMP)Vlcg>/Tmco6<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmco6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263701	F	MP:0001402	decreased locomotor activity	Tmco6<tm1.1(KOMP)Vlcg>/Tmco6<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmco6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263701	F	MP:0010024	increased total body fat amount	Tmco6<tm1.1(KOMP)Vlcg>/Tmco6<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmco6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263701	M	MP:0001489	decreased startle reflex	Tmco6<tm1.1(KOMP)Vlcg>/Tmco6<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmco6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263701	F	MP:0003795	abnormal bone structure	Tmco6<tm1.1(KOMP)Vlcg>/Tmco6<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmco6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263701	M	MP:0002574	increased vertical activity	Tmco6<tm1.1(KOMP)Vlcg>/Tmco6<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmco6<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263703	F	MP:0000691	enlarged spleen	Tmem116<tm1b(EUCOMM)Hmgu>/Tmem116<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tmem116<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263703	F	MP:0002966	decreased circulating alkaline phosphatase level	Tmem116<tm1b(EUCOMM)Hmgu>/Tmem116<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tmem116<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263703	F	MP:0001175	abnormal lung morphology	Tmem116<tm1b(EUCOMM)Hmgu>/Tmem116<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tmem116<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263703	F	MP:0000702	enlarged lymph nodes	Tmem116<tm1b(EUCOMM)Hmgu>/Tmem116<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tmem116<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263703	M	MP:0010052	increased grip strength	Tmem116<tm1b(EUCOMM)Hmgu>/Tmem116<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tmem116<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263703	M	MP:0005292	improved glucose tolerance	Tmem116<tm1b(EUCOMM)Hmgu>/Tmem116<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tmem116<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263703	M	MP:0001486	abnormal startle reflex	Tmem116<tm1b(EUCOMM)Hmgu>/Tmem116<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tmem116<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263703	F	MP:0001303	abnormal lens morphology	Tmem116<tm1b(EUCOMM)Hmgu>/Tmem116<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tmem116<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263703	M	MP:0001262	decreased body weight	Tmem116<tm1b(EUCOMM)Hmgu>/Tmem116<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tmem116<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263704	M	MP:0002060	abnormal skin morphology	Tmem121b<em1(IMPC)Tcp>/Tmem121b<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem121b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263704	M	MP:0005016	decreased lymphocyte cell number	Tmem121b<em1(IMPC)Tcp>/Tmem121b<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem121b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263704	M	MP:0000219	increased neutrophil cell number	Tmem121b<em1(IMPC)Tcp>/Tmem121b<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem121b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263704	M	MP:0002941	increased circulating alanine transaminase level	Tmem121b<em1(IMPC)Tcp>/Tmem121b<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem121b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263706	M	MP:0005178	increased circulating cholesterol level	Tmem129<tm1.1(KOMP)Vlcg>/Tmem129<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem129<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263706	M	MP:0010024	increased total body fat amount	Tmem129<tm1.1(KOMP)Vlcg>/Tmem129<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem129<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263706	F	MP:0002968	increased circulating alkaline phosphatase level	Tmem129<tm1.1(KOMP)Vlcg>/Tmem129<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem129<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263706	F	MP:0001399	hyperactivity	Tmem129<tm1.1(KOMP)Vlcg>/Tmem129<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem129<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263706	M	MP:0003961	decreased lean body mass	Tmem129<tm1.1(KOMP)Vlcg>/Tmem129<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem129<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263706	M	MP:0001556	increased circulating HDL cholesterol level	Tmem129<tm1.1(KOMP)Vlcg>/Tmem129<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem129<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263708	F	MP:0001415	increased exploration in new environment	Tmem14a<tm2b(KOMP)Wtsi>/Tmem14a<+>	C57BL/6N-Tmem14a<tm2b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263709	M	MP:0000274	enlarged heart	Tmem160<em1(IMPC)Tcp>/Tmem160<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem160<em1(IMPC)Tcp>/TcpMmucd	N	MGI:5576271
MGI:6263709	M	MP:0002135	abnormal kidney morphology	Tmem160<em1(IMPC)Tcp>/Tmem160<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem160<em1(IMPC)Tcp>/TcpMmucd	N	MGI:5576271
MGI:6263709	M	MP:0000266	abnormal heart morphology	Tmem160<em1(IMPC)Tcp>/Tmem160<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem160<em1(IMPC)Tcp>/TcpMmucd	N	MGI:5576271
MGI:6263709	F	MP:0002092	abnormal eye morphology	Tmem160<em1(IMPC)Tcp>/Tmem160<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem160<em1(IMPC)Tcp>/TcpMmucd	N	MGI:5576271
MGI:6263709	F	MP:0001120	abnormal uterus morphology	Tmem160<em1(IMPC)Tcp>/Tmem160<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem160<em1(IMPC)Tcp>/TcpMmucd	N	MGI:5576271
MGI:6263709	F	MP:0009709	hydrometra	Tmem160<em1(IMPC)Tcp>/Tmem160<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem160<em1(IMPC)Tcp>/TcpMmucd	N	MGI:5576271
MGI:6263710	M	MP:0010024	increased total body fat amount	Tmem161b<tm2b(EUCOMM)Hmgu>/Tmem161b<+>	C57BL/6N-Tmem161b<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263710	F	MP:0005567	decreased circulating total protein level	Tmem161b<tm2b(EUCOMM)Hmgu>/Tmem161b<+>	C57BL/6N-Tmem161b<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263710	F	MP:0005419	decreased circulating serum albumin level	Tmem161b<tm2b(EUCOMM)Hmgu>/Tmem161b<+>	C57BL/6N-Tmem161b<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263710	M	MP:0003961	decreased lean body mass	Tmem161b<tm2b(EUCOMM)Hmgu>/Tmem161b<+>	C57BL/6N-Tmem161b<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263710	M	MP:0010124	decreased bone mineral content	Tmem161b<tm2b(EUCOMM)Hmgu>/Tmem161b<+>	C57BL/6N-Tmem161b<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263713	F	MP:0013630	increased bone trabecular spacing	Tmem18<tm1b(EUCOMM)Wtsi>/Tmem18<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem18<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263714	M	MP:0000194	increased circulating calcium level	Tmem203<em1(IMPC)H>/Tmem203<em1(IMPC)H>	C57BL/6N-Tmem203<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263714	M	MP:0002833	increased heart weight	Tmem203<em1(IMPC)H>/Tmem203<em1(IMPC)H>	C57BL/6N-Tmem203<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263714	M	MP:0001925	male infertility	Tmem203<em1(IMPC)H>/Tmem203<em1(IMPC)H>	C57BL/6N-Tmem203<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263714	F	MP:0002968	increased circulating alkaline phosphatase level	Tmem203<em1(IMPC)H>/Tmem203<em1(IMPC)H>	C57BL/6N-Tmem203<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263714	M	MP:0000186	decreased circulating HDL cholesterol level	Tmem203<em1(IMPC)H>/Tmem203<em1(IMPC)H>	C57BL/6N-Tmem203<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263714	F	MP:0001325	abnormal retina morphology	Tmem203<em1(IMPC)H>/Tmem203<em1(IMPC)H>	C57BL/6N-Tmem203<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263714	M	MP:0005179	decreased circulating cholesterol level	Tmem203<em1(IMPC)H>/Tmem203<em1(IMPC)H>	C57BL/6N-Tmem203<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263715	M	MP:0000691	enlarged spleen	Tmem209<em1(IMPC)Tcp>/Tmem209<+>	C57BL/6NCrl-Tmem209<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263715	M	MP:0000470	abnormal stomach morphology	Tmem209<em1(IMPC)Tcp>/Tmem209<+>	C57BL/6NCrl-Tmem209<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263715	M	MP:0002059	abnormal seminal vesicle morphology	Tmem209<em1(IMPC)Tcp>/Tmem209<+>	C57BL/6NCrl-Tmem209<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263715	M	MP:0000702	enlarged lymph nodes	Tmem209<em1(IMPC)Tcp>/Tmem209<+>	C57BL/6NCrl-Tmem209<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263716	F	MP:0001711	abnormal placenta morphology	Tmem209<em1(IMPC)Tcp>/Tmem209<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem209<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263716	F	MP:0001297	microphthalmia	Tmem209<em1(IMPC)Tcp>/Tmem209<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem209<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263716	M	MP:0001925	male infertility	Tmem209<em1(IMPC)Tcp>/Tmem209<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem209<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263716	F	MP:0003717	pallor	Tmem209<em1(IMPC)Tcp>/Tmem209<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem209<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263718	M	MP:0006243	impaired pupillary reflex	Tmem222<tm1b(KOMP)Mbp>/Tmem222<+>	C57BL/6N-Tmem222<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263720	M	MP:0013278	decreased fasting circulating glucose level	Tmem260<tm1a(KOMP)Wtsi>/Tmem260<tm1a(KOMP)Wtsi>	C57BL/6N-Tmem260<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263720	M	MP:0010025	decreased total body fat amount	Tmem260<tm1a(KOMP)Wtsi>/Tmem260<tm1a(KOMP)Wtsi>	C57BL/6N-Tmem260<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263720	M	MP:0003960	increased lean body mass	Tmem260<tm1a(KOMP)Wtsi>/Tmem260<tm1a(KOMP)Wtsi>	C57BL/6N-Tmem260<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263721	M	MP:0010053	decreased grip strength	Tmem50b<tm1b(EUCOMM)Wtsi>/Tmem50b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem50b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263721	M	MP:0002699	abnormal vitreous body morphology	Tmem50b<tm1b(EUCOMM)Wtsi>/Tmem50b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem50b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263721	M	MP:0011962	increased cornea thickness	Tmem50b<tm1b(EUCOMM)Wtsi>/Tmem50b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem50b<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263722	M	MP:0001556	increased circulating HDL cholesterol level	Tmem51<tm1b(EUCOMM)Hmgu>/Tmem51<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tmem51<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263722	F	MP:0010088	decreased circulating fructosamine level	Tmem51<tm1b(EUCOMM)Hmgu>/Tmem51<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tmem51<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263722	M	MP:0001325	abnormal retina morphology	Tmem51<tm1b(EUCOMM)Hmgu>/Tmem51<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tmem51<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263723	M	MP:0002631	abnormal epididymis morphology	Tmem74<em1(IMPC)Tcp>/Tmem74<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem74<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263723	M	MP:0000702	enlarged lymph nodes	Tmem74<em1(IMPC)Tcp>/Tmem74<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem74<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263723	M	MP:0000706	small thymus	Tmem74<em1(IMPC)Tcp>/Tmem74<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem74<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263723	M	MP:0002060	abnormal skin morphology	Tmem74<em1(IMPC)Tcp>/Tmem74<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem74<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263723	F	MP:0001126	abnormal ovary morphology	Tmem74<em1(IMPC)Tcp>/Tmem74<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem74<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263723	M	MP:0011874	enlarged urinary bladder	Tmem74<em1(IMPC)Tcp>/Tmem74<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem74<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263723	M	MP:0000691	enlarged spleen	Tmem74<em1(IMPC)Tcp>/Tmem74<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem74<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263723	M	MP:0002059	abnormal seminal vesicle morphology	Tmem74<em1(IMPC)Tcp>/Tmem74<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem74<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263723	M	MP:0002135	abnormal kidney morphology	Tmem74<em1(IMPC)Tcp>/Tmem74<em1(IMPC)Tcp>	C57BL/6NCrl-Tmem74<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263725	F	MP:0000208	decreased hematocrit	Tmem97<tm1.1(KOMP)Vlcg>/Tmem97<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem97<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6263725	F	MP:0002875	decreased erythrocyte cell number	Tmem97<tm1.1(KOMP)Vlcg>/Tmem97<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem97<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6263725	F	MP:0002874	decreased hemoglobin content	Tmem97<tm1.1(KOMP)Vlcg>/Tmem97<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem97<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6263725	F	MP:0010067	increased red blood cell distribution width	Tmem97<tm1.1(KOMP)Vlcg>/Tmem97<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem97<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6263725	M	MP:0001147	small testis	Tmem97<tm1.1(KOMP)Vlcg>/Tmem97<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem97<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6263727	M	MP:0010024	increased total body fat amount	Tmem9b<em1(IMPC)J>/Tmem9b<em1(IMPC)J>	C57BL/6NJ-Tmem9b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263727	M	MP:0002591	decreased mean corpuscular volume	Tmem9b<em1(IMPC)J>/Tmem9b<em1(IMPC)J>	C57BL/6NJ-Tmem9b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263727	M	MP:0005178	increased circulating cholesterol level	Tmem9b<em1(IMPC)J>/Tmem9b<em1(IMPC)J>	C57BL/6NJ-Tmem9b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263727	M	MP:0001556	increased circulating HDL cholesterol level	Tmem9b<em1(IMPC)J>/Tmem9b<em1(IMPC)J>	C57BL/6NJ-Tmem9b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263728	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Tmprss6<tm1b(EUCOMM)Wtsi>/Tmprss6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmprss6<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263728	F	MP:0005387	immune system phenotype	Tmprss6<tm1b(EUCOMM)Wtsi>/Tmprss6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmprss6<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263728	M	MP:0005562	decreased mean corpuscular hemoglobin	Tmprss6<tm1b(EUCOMM)Wtsi>/Tmprss6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmprss6<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263728	M	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Tmprss6<tm1b(EUCOMM)Wtsi>/Tmprss6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmprss6<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263728	M	MP:0008045	decreased NK cell number	Tmprss6<tm1b(EUCOMM)Wtsi>/Tmprss6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmprss6<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263728	M	MP:0002833	increased heart weight	Tmprss6<tm1b(EUCOMM)Wtsi>/Tmprss6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmprss6<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263728	M	MP:0000208	decreased hematocrit	Tmprss6<tm1b(EUCOMM)Wtsi>/Tmprss6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmprss6<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263728	M	MP:0002874	decreased hemoglobin content	Tmprss6<tm1b(EUCOMM)Wtsi>/Tmprss6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmprss6<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263728	M	MP:0002591	decreased mean corpuscular volume	Tmprss6<tm1b(EUCOMM)Wtsi>/Tmprss6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmprss6<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263728	M	MP:0013648	increased CD11b-high dendritic cell number	Tmprss6<tm1b(EUCOMM)Wtsi>/Tmprss6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmprss6<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6263730	F	MP:0005016	decreased lymphocyte cell number	Tmub2<tm1b(KOMP)Wtsi>/Tmub2<tm1b(KOMP)Wtsi>	C57BL/6N-Tmub2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263730	M	MP:0000266	abnormal heart morphology	Tmub2<tm1b(KOMP)Wtsi>/Tmub2<tm1b(KOMP)Wtsi>	C57BL/6N-Tmub2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263730	F	MP:0009709	hydrometra	Tmub2<tm1b(KOMP)Wtsi>/Tmub2<tm1b(KOMP)Wtsi>	C57BL/6N-Tmub2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263730	M	MP:0000274	enlarged heart	Tmub2<tm1b(KOMP)Wtsi>/Tmub2<tm1b(KOMP)Wtsi>	C57BL/6N-Tmub2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263730	F	MP:0001102	small superior vagus ganglion	Tmub2<tm1b(KOMP)Wtsi>/Tmub2<tm1b(KOMP)Wtsi>	C57BL/6N-Tmub2<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263732	M	MP:0005011	increased eosinophil cell number	Tnfrsf1a<tm2b(EUCOMM)Wtsi>/Tnfrsf1a<tm2b(EUCOMM)Wtsi>	C57BL/6N-Tnfrsf1a<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263732	F	MP:0000223	decreased monocyte cell number	Tnfrsf1a<tm2b(EUCOMM)Wtsi>/Tnfrsf1a<tm2b(EUCOMM)Wtsi>	C57BL/6N-Tnfrsf1a<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263732	F	MP:0000222	decreased neutrophil cell number	Tnfrsf1a<tm2b(EUCOMM)Wtsi>/Tnfrsf1a<tm2b(EUCOMM)Wtsi>	C57BL/6N-Tnfrsf1a<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263732	M	MP:0000195	decreased circulating calcium level	Tnfrsf1a<tm2b(EUCOMM)Wtsi>/Tnfrsf1a<tm2b(EUCOMM)Wtsi>	C57BL/6N-Tnfrsf1a<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6263734	M	MP:0001488	increased startle reflex	Tnks2<tm1b(KOMP)Wtsi>/Tnks2<tm1b(KOMP)Wtsi>	C57BL/6N-Tnks2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263734	F	MP:0010052	increased grip strength	Tnks2<tm1b(KOMP)Wtsi>/Tnks2<tm1b(KOMP)Wtsi>	C57BL/6N-Tnks2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263737	M	MP:0005560	decreased circulating glucose level	Tnni2<tm1.1(KOMP)Vlcg>/Tnni2<+>	C57BL/6N-Tnni2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263737	M	MP:0010025	decreased total body fat amount	Tnni2<tm1.1(KOMP)Vlcg>/Tnni2<+>	C57BL/6N-Tnni2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263737	M	MP:0002060	abnormal skin morphology	Tnni2<tm1.1(KOMP)Vlcg>/Tnni2<+>	C57BL/6N-Tnni2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263737	M	MP:0013278	decreased fasting circulating glucose level	Tnni2<tm1.1(KOMP)Vlcg>/Tnni2<+>	C57BL/6N-Tnni2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263740	F	MP:0001399	hyperactivity	Tomm40<em1(IMPC)J>/Tomm40<+>	C57BL/6NJ-Tomm40<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263740	F	MP:0001486	abnormal startle reflex	Tomm40<em1(IMPC)J>/Tomm40<+>	C57BL/6NJ-Tomm40<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263740	M	MP:0001304	cataract	Tomm40<em1(IMPC)J>/Tomm40<+>	C57BL/6NJ-Tomm40<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263744	M	MP:0000274	enlarged heart	Toporsl<tm1.1(KOMP)Vlcg>/Toporsl<tm1.1(KOMP)Vlcg>	C57BL/6N-Toporsl<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263744	M	MP:0000266	abnormal heart morphology	Toporsl<tm1.1(KOMP)Vlcg>/Toporsl<tm1.1(KOMP)Vlcg>	C57BL/6N-Toporsl<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263746	M	MP:0010024	increased total body fat amount	Tox2<em1(IMPC)H>/Tox2<em1(IMPC)H>	C57BL/6NTac-Tox2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263746	F	MP:0001402	decreased locomotor activity	Tox2<em1(IMPC)H>/Tox2<em1(IMPC)H>	C57BL/6NTac-Tox2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263746	M	MP:0002764	short tibia	Tox2<em1(IMPC)H>/Tox2<em1(IMPC)H>	C57BL/6NTac-Tox2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263747	F	MP:0001417	decreased exploration in new environment	Tox3<em1(IMPC)Tcp>/Tox3<+>	C57BL/6NCrl-Tox3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263748	F	MP:0005553	increased circulating creatinine level	Tox4<tm1b(KOMP)Mbp>/Tox4<+>	C57BL/6N-Tox4<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263748	M	MP:0005560	decreased circulating glucose level	Tox4<tm1b(KOMP)Mbp>/Tox4<+>	C57BL/6N-Tox4<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263749	F	MP:0003984	embryonic growth retardation	Tox4<tm1b(KOMP)Mbp>/Tox4<tm1b(KOMP)Mbp>	C57BL/6N-Tox4<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263750	F	MP:0000266	abnormal heart morphology	Tox<tm1b(KOMP)Wtsi>/Tox<tm1b(KOMP)Wtsi>	C57BL/6N-Tox<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263750	M	MP:0004952	increased spleen weight	Tox<tm1b(KOMP)Wtsi>/Tox<tm1b(KOMP)Wtsi>	C57BL/6N-Tox<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263750	F	MP:0010124	decreased bone mineral content	Tox<tm1b(KOMP)Wtsi>/Tox<tm1b(KOMP)Wtsi>	C57BL/6N-Tox<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263750	F	MP:0002968	increased circulating alkaline phosphatase level	Tox<tm1b(KOMP)Wtsi>/Tox<tm1b(KOMP)Wtsi>	C57BL/6N-Tox<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263750	M	MP:0005179	decreased circulating cholesterol level	Tox<tm1b(KOMP)Wtsi>/Tox<tm1b(KOMP)Wtsi>	C57BL/6N-Tox<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263750	M	MP:0001486	abnormal startle reflex	Tox<tm1b(KOMP)Wtsi>/Tox<tm1b(KOMP)Wtsi>	C57BL/6N-Tox<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263750	F	MP:0000063	decreased bone mineral density	Tox<tm1b(KOMP)Wtsi>/Tox<tm1b(KOMP)Wtsi>	C57BL/6N-Tox<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263750	F	MP:0000274	enlarged heart	Tox<tm1b(KOMP)Wtsi>/Tox<tm1b(KOMP)Wtsi>	C57BL/6N-Tox<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6263752	F	MP:0001304	cataract	Tpk1<em1(IMPC)J>/Tpk1<+>	C57BL/6NJ-Tpk1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263757	M	MP:0002989	small kidney	Trappc1<em1(IMPC)Mbp>/Trappc1<+>	C57BL/6NCrl-Trappc1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263757	M	MP:0001146	abnormal testis morphology	Trappc1<em1(IMPC)Mbp>/Trappc1<+>	C57BL/6NCrl-Trappc1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263757	M	MP:0000598	abnormal liver morphology	Trappc1<em1(IMPC)Mbp>/Trappc1<+>	C57BL/6NCrl-Trappc1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263757	M	MP:0002997	enlarged seminal vesicle	Trappc1<em1(IMPC)Mbp>/Trappc1<+>	C57BL/6NCrl-Trappc1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263757	M	MP:0009552	urinary bladder obstruction	Trappc1<em1(IMPC)Mbp>/Trappc1<+>	C57BL/6NCrl-Trappc1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263757	M	MP:0001148	enlarged testis	Trappc1<em1(IMPC)Mbp>/Trappc1<+>	C57BL/6NCrl-Trappc1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263757	M	MP:0002135	abnormal kidney morphology	Trappc1<em1(IMPC)Mbp>/Trappc1<+>	C57BL/6NCrl-Trappc1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263757	F	MP:0002060	abnormal skin morphology	Trappc1<em1(IMPC)Mbp>/Trappc1<+>	C57BL/6NCrl-Trappc1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263757	M	MP:0001147	small testis	Trappc1<em1(IMPC)Mbp>/Trappc1<+>	C57BL/6NCrl-Trappc1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263758	F	MP:0001417	decreased exploration in new environment	Trarg1<em2(IMPC)Tcp>/Trarg1<em2(IMPC)Tcp>	C57BL/6NCrl-Trarg1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263758	F	MP:0001402	decreased locomotor activity	Trarg1<em2(IMPC)Tcp>/Trarg1<em2(IMPC)Tcp>	C57BL/6NCrl-Trarg1<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263763	F	MP:0002989	small kidney	Trh<em1(IMPC)Tcp>/Trh<em1(IMPC)Tcp>	C57BL/6NCrl-Trh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263763	F	MP:0000062	increased bone mineral density	Trh<em1(IMPC)Tcp>/Trh<em1(IMPC)Tcp>	C57BL/6NCrl-Trh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263763	F	MP:0001556	increased circulating HDL cholesterol level	Trh<em1(IMPC)Tcp>/Trh<em1(IMPC)Tcp>	C57BL/6NCrl-Trh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263763	M	MP:0002834	decreased heart weight	Trh<em1(IMPC)Tcp>/Trh<em1(IMPC)Tcp>	C57BL/6NCrl-Trh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263763	M	MP:0000470	abnormal stomach morphology	Trh<em1(IMPC)Tcp>/Trh<em1(IMPC)Tcp>	C57BL/6NCrl-Trh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263763	F	MP:0010123	increased bone mineral content	Trh<em1(IMPC)Tcp>/Trh<em1(IMPC)Tcp>	C57BL/6NCrl-Trh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263763	F	MP:0005553	increased circulating creatinine level	Trh<em1(IMPC)Tcp>/Trh<em1(IMPC)Tcp>	C57BL/6NCrl-Trh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263763	M	MP:0002188	small heart	Trh<em1(IMPC)Tcp>/Trh<em1(IMPC)Tcp>	C57BL/6NCrl-Trh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263764	M	MP:0001510	abnormal coat appearance	Trib1<tm1b(KOMP)Wtsi>/Trib1<+>	C57BL/6N-Trib1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263764	M	MP:0011239	abnormal skin coloration	Trib1<tm1b(KOMP)Wtsi>/Trib1<+>	C57BL/6N-Trib1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263765	M	MP:0011965	decreased total retina thickness	Trib2<tm1b(KOMP)Wtsi>/Trib2<tm1b(KOMP)Wtsi>	C57BL/6N-Trib2<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263765	M	MP:0003731	abnormal retina outer nuclear layer morphology	Trib2<tm1b(KOMP)Wtsi>/Trib2<tm1b(KOMP)Wtsi>	C57BL/6N-Trib2<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263765	M	MP:0003733	abnormal retina inner nuclear layer morphology	Trib2<tm1b(KOMP)Wtsi>/Trib2<tm1b(KOMP)Wtsi>	C57BL/6N-Trib2<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263765	M	MP:0001399	hyperactivity	Trib2<tm1b(KOMP)Wtsi>/Trib2<tm1b(KOMP)Wtsi>	C57BL/6N-Trib2<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263766	M	MP:0004509	abnormal pelvic girdle bone morphology	Trim17<tm1e(EUCOMM)Wtsi>/Trim17<tm1e(EUCOMM)Wtsi>	C57BL/6N-Trim17<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263768	M	MP:0010052	increased grip strength	Trim29<tm1a(EUCOMM)Wtsi>/Trim29<tm1a(EUCOMM)Wtsi>	C57BL/6N-Trim29<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263769	M	MP:0013279	increased fasting circulating glucose level	Trim39<tm1b(EUCOMM)Hmgu>/Trim39<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trim39<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263769	M	MP:0001284	absent vibrissae	Trim39<tm1b(EUCOMM)Hmgu>/Trim39<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trim39<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263769	M	MP:0000218	increased leukocyte cell number	Trim39<tm1b(EUCOMM)Hmgu>/Trim39<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trim39<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263769	M	MP:0012362	increased large unstained cell number	Trim39<tm1b(EUCOMM)Hmgu>/Trim39<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trim39<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263770	M	MP:0010506	prolonged RR interval	Trim55<tm2b(EUCOMM)Hmgu>/Trim55<tm2b(EUCOMM)Hmgu>	C57BL/6N-Trim55<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263770	M	MP:0005333	decreased heart rate	Trim55<tm2b(EUCOMM)Hmgu>/Trim55<tm2b(EUCOMM)Hmgu>	C57BL/6N-Trim55<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263770	M	MP:0013278	decreased fasting circulating glucose level	Trim55<tm2b(EUCOMM)Hmgu>/Trim55<tm2b(EUCOMM)Hmgu>	C57BL/6N-Trim55<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263773	F	MP:0000186	decreased circulating HDL cholesterol level	Trim8<em1(IMPC)Wtsi>/Trim8<em1(IMPC)Wtsi>	C57BL/6N-Trim8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263773	F	MP:0005561	increased mean corpuscular hemoglobin	Trim8<em1(IMPC)Wtsi>/Trim8<em1(IMPC)Wtsi>	C57BL/6N-Trim8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263773	F	MP:0005419	decreased circulating serum albumin level	Trim8<em1(IMPC)Wtsi>/Trim8<em1(IMPC)Wtsi>	C57BL/6N-Trim8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263774	F	MP:0010124	decreased bone mineral content	Trip13<em1(IMPC)J>/Trip13<em1(IMPC)J>	C57BL/6NJ-Trip13<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263774	F	MP:0000063	decreased bone mineral density	Trip13<em1(IMPC)J>/Trip13<em1(IMPC)J>	C57BL/6NJ-Trip13<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263774	M	MP:0001925	male infertility	Trip13<em1(IMPC)J>/Trip13<em1(IMPC)J>	C57BL/6NJ-Trip13<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263774	F	MP:0001926	female infertility	Trip13<em1(IMPC)J>/Trip13<em1(IMPC)J>	C57BL/6NJ-Trip13<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263774	F	MP:0011396	abnormal sleep behavior	Trip13<em1(IMPC)J>/Trip13<em1(IMPC)J>	C57BL/6NJ-Trip13<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263777	F	MP:0010091	decreased circulating creatine kinase level	Trp53<tm1b(EUCOMM)Hmgu>/Trp53<+>	C57BL/6N-Trp53<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263778	M	MP:0012362	increased large unstained cell number	Trp53<tm1b(EUCOMM)Hmgu>/Trp53<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trp53<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263778	F	MP:0001488	increased startle reflex	Trp53<tm1b(EUCOMM)Hmgu>/Trp53<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trp53<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263779	F	MP:0005565	increased blood urea nitrogen level	Trp73<em1(IMPC)H>/Trp73<+>	C57BL/6NTac-Trp73<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263779	M	MP:0005505	thrombocytosis	Trp73<em1(IMPC)H>/Trp73<+>	C57BL/6NTac-Trp73<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263779	M	MP:0005011	increased eosinophil cell number	Trp73<em1(IMPC)H>/Trp73<+>	C57BL/6NTac-Trp73<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263781	F	MP:0011960	abnormal eye anterior chamber depth	Trpm6<tm1b(KOMP)Wtsi>/Trpm6<+>	C57BL/6N-Trpm6<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6263781	M	MP:0001257	increased body length	Trpm6<tm1b(KOMP)Wtsi>/Trpm6<+>	C57BL/6N-Trpm6<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6263781	M	MP:0010052	increased grip strength	Trpm6<tm1b(KOMP)Wtsi>/Trpm6<+>	C57BL/6N-Trpm6<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6263781	M	MP:0000198	decreased circulating phosphate level	Trpm6<tm1b(KOMP)Wtsi>/Trpm6<+>	C57BL/6N-Trpm6<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6263782	M	MP:0005505	thrombocytosis	Trpm7<tm1b(KOMP)Wtsi>/Trpm7<+>	C57BL/6N-Trpm7<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6263786	F	MP:0005343	increased circulating aspartate transaminase level	Trub1<tm1b(EUCOMM)Hmgu>/Trub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trub1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263786	F	MP:0010090	increased circulating creatine kinase level	Trub1<tm1b(EUCOMM)Hmgu>/Trub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trub1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263786	F	MP:0005554	decreased circulating creatinine level	Trub1<tm1b(EUCOMM)Hmgu>/Trub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trub1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263788	F	MP:0003795	abnormal bone structure	Tsks<em1(IMPC)Wtsi>/Tsks<em1(IMPC)Wtsi>	C57BL/6N-Tsks<em1(IMPC)Wtsi>/WtsiCnrm	N	MGI:5576271
MGI:6263788	M	MP:0001925	male infertility	Tsks<em1(IMPC)Wtsi>/Tsks<em1(IMPC)Wtsi>	C57BL/6N-Tsks<em1(IMPC)Wtsi>/WtsiCnrm	N	MGI:5576271
MGI:6263790	F	MP:0001399	hyperactivity	Tspyl2<tm1b(KOMP)Wtsi>/Tspyl2<tm1b(KOMP)Wtsi>	C57BL/6N-Tspyl2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263791	F	MP:0000194	increased circulating calcium level	Ttc39a<tm1b(KOMP)Mbp>/Ttc39a<tm1b(KOMP)Mbp>	C57BL/6N-Ttc39a<tm1b(KOMP)Mbp>/Orl	N	MGI:5576271
MGI:6263791	F	MP:0002833	increased heart weight	Ttc39a<tm1b(KOMP)Mbp>/Ttc39a<tm1b(KOMP)Mbp>	C57BL/6N-Ttc39a<tm1b(KOMP)Mbp>/Orl	N	MGI:5576271
MGI:6263791	F	MP:0001566	increased circulating phosphate level	Ttc39a<tm1b(KOMP)Mbp>/Ttc39a<tm1b(KOMP)Mbp>	C57BL/6N-Ttc39a<tm1b(KOMP)Mbp>/Orl	N	MGI:5576271
MGI:6263794	M	MP:0011939	increased food intake	Tuba3a<tm1b(KOMP)Wtsi>/Tuba3a<tm1b(KOMP)Wtsi>	C57BL/6N-Tuba3a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263796	M	MP:0010024	increased total body fat amount	Tusc1<em1(IMPC)J>/Tusc1<em1(IMPC)J>	C57BL/6NJ-Tusc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263797	F	MP:0003385	abnormal body wall morphology	Tusc3<em1(IMPC)J>/Tusc3<em1(IMPC)J>	C57BL/6NJ-Tusc3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263797	M	MP:0001697	abnormal embryo size	Tusc3<em1(IMPC)J>/Tusc3<em1(IMPC)J>	C57BL/6NJ-Tusc3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263801	M	MP:0001406	abnormal gait	Txlna<tm1b(EUCOMM)Hmgu>/Txlna<+>	C57BL/6N-Txlna<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263801	M	MP:0012362	increased large unstained cell number	Txlna<tm1b(EUCOMM)Hmgu>/Txlna<+>	C57BL/6N-Txlna<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263801	F	MP:0002874	decreased hemoglobin content	Txlna<tm1b(EUCOMM)Hmgu>/Txlna<+>	C57BL/6N-Txlna<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263802	M	MP:0001147	small testis	Txlna<tm1b(EUCOMM)Hmgu>/Txlna<tm1b(EUCOMM)Hmgu>	C57BL/6N-Txlna<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263802	F	MP:0005013	increased lymphocyte cell number	Txlna<tm1b(EUCOMM)Hmgu>/Txlna<tm1b(EUCOMM)Hmgu>	C57BL/6N-Txlna<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263802	M	MP:0001417	decreased exploration in new environment	Txlna<tm1b(EUCOMM)Hmgu>/Txlna<tm1b(EUCOMM)Hmgu>	C57BL/6N-Txlna<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263802	F	MP:0012362	increased large unstained cell number	Txlna<tm1b(EUCOMM)Hmgu>/Txlna<tm1b(EUCOMM)Hmgu>	C57BL/6N-Txlna<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263802	M	MP:0005627	increased circulating potassium level	Txlna<tm1b(EUCOMM)Hmgu>/Txlna<tm1b(EUCOMM)Hmgu>	C57BL/6N-Txlna<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6263803	M	MP:0001944	abnormal pancreas morphology	Tyk2<tm2b(EUCOMM)Hmgu>/Tyk2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Tyk2<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263803	M	MP:0000709	enlarged thymus	Tyk2<tm2b(EUCOMM)Hmgu>/Tyk2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Tyk2<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263803	F	MP:0001126	abnormal ovary morphology	Tyk2<tm2b(EUCOMM)Hmgu>/Tyk2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Tyk2<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263803	M	MP:0000691	enlarged spleen	Tyk2<tm2b(EUCOMM)Hmgu>/Tyk2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Tyk2<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263803	M	MP:0002059	abnormal seminal vesicle morphology	Tyk2<tm2b(EUCOMM)Hmgu>/Tyk2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Tyk2<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263804	M	MP:0005419	decreased circulating serum albumin level	Tyw1<tm1b(KOMP)Wtsi>/Tyw1<tm1b(KOMP)Wtsi>	C57BL/6N-Tyw1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263804	F	MP:0000208	decreased hematocrit	Tyw1<tm1b(KOMP)Wtsi>/Tyw1<tm1b(KOMP)Wtsi>	C57BL/6N-Tyw1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263804	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Tyw1<tm1b(KOMP)Wtsi>/Tyw1<tm1b(KOMP)Wtsi>	C57BL/6N-Tyw1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263804	F	MP:0001417	decreased exploration in new environment	Tyw1<tm1b(KOMP)Wtsi>/Tyw1<tm1b(KOMP)Wtsi>	C57BL/6N-Tyw1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263804	M	MP:0006243	impaired pupillary reflex	Tyw1<tm1b(KOMP)Wtsi>/Tyw1<tm1b(KOMP)Wtsi>	C57BL/6N-Tyw1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263807	M	MP:0010097	abnormal retina blood vessel morphology	Ube2a<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Ube2a<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263807	M	MP:0001399	hyperactivity	Ube2a<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Ube2a<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263808	F	MP:0002833	increased heart weight	Ube2a<tm1.1(KOMP)Vlcg>/Ube2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Ube2a<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263808	F	MP:0010053	decreased grip strength	Ube2a<tm1.1(KOMP)Vlcg>/Ube2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Ube2a<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263808	F	MP:0001488	increased startle reflex	Ube2a<tm1.1(KOMP)Vlcg>/Ube2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Ube2a<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263808	F	MP:0005419	decreased circulating serum albumin level	Ube2a<tm1.1(KOMP)Vlcg>/Ube2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Ube2a<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263808	F	MP:0001402	decreased locomotor activity	Ube2a<tm1.1(KOMP)Vlcg>/Ube2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Ube2a<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263808	F	MP:0001926	female infertility	Ube2a<tm1.1(KOMP)Vlcg>/Ube2a<tm1.1(KOMP)Vlcg>	C57BL/6N-Ube2a<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263809	M	MP:0002590	increased mean corpuscular volume	Ube2e2<tm1b(KOMP)Wtsi>/Ube2e2<tm1b(KOMP)Wtsi>	C57BL/6N-Ube2e2<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6263810	M	MP:0003425	abnormal optic vesicle formation	Ube2f<em1(IMPC)Mbp>/Ube2f<em1(IMPC)Mbp>	C57BL/6NCrl-Ube2f<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263810	M	MP:0005650	abnormal limb bud morphology	Ube2f<em1(IMPC)Mbp>/Ube2f<em1(IMPC)Mbp>	C57BL/6NCrl-Ube2f<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263810	F	MP:0000288	abnormal pericardium morphology	Ube2f<em1(IMPC)Mbp>/Ube2f<em1(IMPC)Mbp>	C57BL/6NCrl-Ube2f<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263812	M	MP:0001312	abnormal cornea morphology	Ubiad1<em1(IMPC)J>/Ubiad1<+>	C57BL/6NJ-Ubiad1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263812	F	MP:0002075	abnormal coat/hair pigmentation	Ubiad1<em1(IMPC)J>/Ubiad1<+>	C57BL/6NJ-Ubiad1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263814	F	MP:0001513	limb grasping	Ubn1<em1(IMPC)J>/Ubn1<em1(IMPC)J>	C57BL/6NJ-Ubn1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263814	M	MP:0001488	increased startle reflex	Ubn1<em1(IMPC)J>/Ubn1<em1(IMPC)J>	C57BL/6NJ-Ubn1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263814	M	MP:0002941	increased circulating alanine transaminase level	Ubn1<em1(IMPC)J>/Ubn1<em1(IMPC)J>	C57BL/6NJ-Ubn1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263815	F	MP:0001697	abnormal embryo size	Ubp1<tm1b(KOMP)Mbp>/Ubp1<tm1b(KOMP)Mbp>	C57BL/6N-Ubp1<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6263815	F	MP:0003717	pallor	Ubp1<tm1b(KOMP)Mbp>/Ubp1<tm1b(KOMP)Mbp>	C57BL/6N-Ubp1<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6263815	F	MP:0001722	pale yolk sac	Ubp1<tm1b(KOMP)Mbp>/Ubp1<tm1b(KOMP)Mbp>	C57BL/6N-Ubp1<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6263816	M	MP:0000274	enlarged heart	Ubr2<tm1e.1(KOMP)Mbp>/Ubr2<+>	C57BL/6N-Ubr2<tm1e.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6263816	M	MP:0000266	abnormal heart morphology	Ubr2<tm1e.1(KOMP)Mbp>/Ubr2<+>	C57BL/6N-Ubr2<tm1e.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6263816	F	MP:0000598	abnormal liver morphology	Ubr2<tm1e.1(KOMP)Mbp>/Ubr2<+>	C57BL/6N-Ubr2<tm1e.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6263819	M	MP:0010090	increased circulating creatine kinase level	Ubxn10<tm1b(EUCOMM)Wtsi>/Ubxn10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ubxn10<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263819	M	MP:0002941	increased circulating alanine transaminase level	Ubxn10<tm1b(EUCOMM)Wtsi>/Ubxn10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ubxn10<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263823	M	MP:0001147	small testis	Ulk3<em2(IMPC)Tcp>/Ulk3<em2(IMPC)Tcp>	C57BL/6NCrl-Ulk3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263823	M	MP:0005419	decreased circulating serum albumin level	Ulk3<em2(IMPC)Tcp>/Ulk3<em2(IMPC)Tcp>	C57BL/6NCrl-Ulk3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263823	M	MP:0002631	abnormal epididymis morphology	Ulk3<em2(IMPC)Tcp>/Ulk3<em2(IMPC)Tcp>	C57BL/6NCrl-Ulk3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263823	M	MP:0002339	abnormal lymph node morphology	Ulk3<em2(IMPC)Tcp>/Ulk3<em2(IMPC)Tcp>	C57BL/6NCrl-Ulk3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263823	F	MP:0005178	increased circulating cholesterol level	Ulk3<em2(IMPC)Tcp>/Ulk3<em2(IMPC)Tcp>	C57BL/6NCrl-Ulk3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263823	F	MP:0001120	abnormal uterus morphology	Ulk3<em2(IMPC)Tcp>/Ulk3<em2(IMPC)Tcp>	C57BL/6NCrl-Ulk3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263823	M	MP:0005633	increased circulating sodium level	Ulk3<em2(IMPC)Tcp>/Ulk3<em2(IMPC)Tcp>	C57BL/6NCrl-Ulk3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263823	M	MP:0004958	enlarged prostate gland	Ulk3<em2(IMPC)Tcp>/Ulk3<em2(IMPC)Tcp>	C57BL/6NCrl-Ulk3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263823	M	MP:0000689	abnormal spleen morphology	Ulk3<em2(IMPC)Tcp>/Ulk3<em2(IMPC)Tcp>	C57BL/6NCrl-Ulk3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263823	M	MP:0002059	abnormal seminal vesicle morphology	Ulk3<em2(IMPC)Tcp>/Ulk3<em2(IMPC)Tcp>	C57BL/6NCrl-Ulk3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263823	M	MP:0011874	enlarged urinary bladder	Ulk3<em2(IMPC)Tcp>/Ulk3<em2(IMPC)Tcp>	C57BL/6NCrl-Ulk3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263823	F	MP:0005553	increased circulating creatinine level	Ulk3<em2(IMPC)Tcp>/Ulk3<em2(IMPC)Tcp>	C57BL/6NCrl-Ulk3<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263825	F	MP:0010024	increased total body fat amount	Upb1<tm1a(EUCOMM)Wtsi>/Upb1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Upb1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263825	F	MP:0001258	decreased body length	Upb1<tm1a(EUCOMM)Wtsi>/Upb1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Upb1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263825	F	MP:0003961	decreased lean body mass	Upb1<tm1a(EUCOMM)Wtsi>/Upb1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Upb1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263826	M	MP:0001146	abnormal testis morphology	Upf3a<em1(IMPC)Mbp>/Upf3a<em1(IMPC)Mbp>	C57BL/6NCrl-Upf3a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263826	M	MP:0001925	male infertility	Upf3a<em1(IMPC)Mbp>/Upf3a<em1(IMPC)Mbp>	C57BL/6NCrl-Upf3a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263826	M	MP:0001147	small testis	Upf3a<em1(IMPC)Mbp>/Upf3a<em1(IMPC)Mbp>	C57BL/6NCrl-Upf3a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263826	F	MP:0002092	abnormal eye morphology	Upf3a<em1(IMPC)Mbp>/Upf3a<em1(IMPC)Mbp>	C57BL/6NCrl-Upf3a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263826	F	MP:0001417	decreased exploration in new environment	Upf3a<em1(IMPC)Mbp>/Upf3a<em1(IMPC)Mbp>	C57BL/6NCrl-Upf3a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263827	M	MP:0000706	small thymus	Upf3b<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Upf3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263827	M	MP:0005016	decreased lymphocyte cell number	Upf3b<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Upf3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263827	M	MP:0001399	hyperactivity	Upf3b<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Upf3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263827	M	MP:0000157	abnormal sternum morphology	Upf3b<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Upf3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263827	M	MP:0000221	decreased leukocyte cell number	Upf3b<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Upf3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263827	M	MP:0002989	small kidney	Upf3b<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Upf3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263828	F	MP:0000219	increased neutrophil cell number	Upf3b<em1(IMPC)Tcp>/Upf3b<em1(IMPC)Tcp>	C57BL/6NCrl-Upf3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263828	F	MP:0020422	decreased freezing behavior	Upf3b<em1(IMPC)Tcp>/Upf3b<em1(IMPC)Tcp>	C57BL/6NCrl-Upf3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263828	F	MP:0000706	small thymus	Upf3b<em1(IMPC)Tcp>/Upf3b<em1(IMPC)Tcp>	C57BL/6NCrl-Upf3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263828	F	MP:0002574	increased vertical activity	Upf3b<em1(IMPC)Tcp>/Upf3b<em1(IMPC)Tcp>	C57BL/6NCrl-Upf3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263828	F	MP:0000470	abnormal stomach morphology	Upf3b<em1(IMPC)Tcp>/Upf3b<em1(IMPC)Tcp>	C57BL/6NCrl-Upf3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263828	F	MP:0001399	hyperactivity	Upf3b<em1(IMPC)Tcp>/Upf3b<em1(IMPC)Tcp>	C57BL/6NCrl-Upf3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263828	F	MP:0005016	decreased lymphocyte cell number	Upf3b<em1(IMPC)Tcp>/Upf3b<em1(IMPC)Tcp>	C57BL/6NCrl-Upf3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263831	F	MP:0010024	increased total body fat amount	Usp13<tm1b(EUCOMM)Hmgu>/Usp13<tm1b(EUCOMM)Hmgu>	C57BL/6N-Usp13<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263831	F	MP:0003961	decreased lean body mass	Usp13<tm1b(EUCOMM)Hmgu>/Usp13<tm1b(EUCOMM)Hmgu>	C57BL/6N-Usp13<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263832	M	MP:0005560	decreased circulating glucose level	Usp15<tm1b(EUCOMM)Wtsi>/Usp15<tm1b(EUCOMM)Wtsi>	C57BL/6N-Usp15<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263832	M	MP:0013278	decreased fasting circulating glucose level	Usp15<tm1b(EUCOMM)Wtsi>/Usp15<tm1b(EUCOMM)Wtsi>	C57BL/6N-Usp15<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263832	M	MP:0003960	increased lean body mass	Usp15<tm1b(EUCOMM)Wtsi>/Usp15<tm1b(EUCOMM)Wtsi>	C57BL/6N-Usp15<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263832	F	MP:0000218	increased leukocyte cell number	Usp15<tm1b(EUCOMM)Wtsi>/Usp15<tm1b(EUCOMM)Wtsi>	C57BL/6N-Usp15<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263832	M	MP:0010025	decreased total body fat amount	Usp15<tm1b(EUCOMM)Wtsi>/Usp15<tm1b(EUCOMM)Wtsi>	C57BL/6N-Usp15<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263832	F	MP:0010088	decreased circulating fructosamine level	Usp15<tm1b(EUCOMM)Wtsi>/Usp15<tm1b(EUCOMM)Wtsi>	C57BL/6N-Usp15<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263833	M	MP:0005561	increased mean corpuscular hemoglobin	Usp19<tm1b(EUCOMM)Hmgu>/Usp19<+>	C57BL/6N-Usp19<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263833	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Usp19<tm1b(EUCOMM)Hmgu>/Usp19<+>	C57BL/6N-Usp19<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263833	M	MP:0001510	abnormal coat appearance	Usp19<tm1b(EUCOMM)Hmgu>/Usp19<+>	C57BL/6N-Usp19<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263833	M	MP:0003960	increased lean body mass	Usp19<tm1b(EUCOMM)Hmgu>/Usp19<+>	C57BL/6N-Usp19<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263834	M	MP:0001925	male infertility	Usp19<tm1b(EUCOMM)Hmgu>/Usp19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Usp19<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6263835	M	MP:0000443	abnormal snout morphology	Usp1<tm1b(KOMP)Wtsi>/Usp1<tm1b(KOMP)Wtsi>	C57BL/6N-Usp1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263835	M	MP:0005565	increased blood urea nitrogen level	Usp1<tm1b(KOMP)Wtsi>/Usp1<tm1b(KOMP)Wtsi>	C57BL/6N-Usp1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263835	M	MP:0002875	decreased erythrocyte cell number	Usp1<tm1b(KOMP)Wtsi>/Usp1<tm1b(KOMP)Wtsi>	C57BL/6N-Usp1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263835	M	MP:0005553	increased circulating creatinine level	Usp1<tm1b(KOMP)Wtsi>/Usp1<tm1b(KOMP)Wtsi>	C57BL/6N-Usp1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263835	F	MP:0001258	decreased body length	Usp1<tm1b(KOMP)Wtsi>/Usp1<tm1b(KOMP)Wtsi>	C57BL/6N-Usp1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263835	M	MP:0002079	increased circulating insulin level	Usp1<tm1b(KOMP)Wtsi>/Usp1<tm1b(KOMP)Wtsi>	C57BL/6N-Usp1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263836	F	MP:0009142	decreased prepulse inhibition	Usp29<em1(IMPC)Tcp>/Usp29<em1(IMPC)Tcp>	C57BL/6NCrl-Usp29<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263836	F	MP:0001417	decreased exploration in new environment	Usp29<em1(IMPC)Tcp>/Usp29<em1(IMPC)Tcp>	C57BL/6NCrl-Usp29<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263836	F	MP:0002060	abnormal skin morphology	Usp29<em1(IMPC)Tcp>/Usp29<em1(IMPC)Tcp>	C57BL/6NCrl-Usp29<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263842	M	MP:0001486	abnormal startle reflex	Ust<em1(IMPC)J>/Ust<+>	C57BL/6NJ-Ust<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263844	M	MP:0000218	increased leukocyte cell number	Utp4<em1(IMPC)J>/Utp4<+>	C57BL/6NJ-Utp4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263844	M	MP:0001284	absent vibrissae	Utp4<em1(IMPC)J>/Utp4<+>	C57BL/6NJ-Utp4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263844	F	MP:0002968	increased circulating alkaline phosphatase level	Utp4<em1(IMPC)J>/Utp4<+>	C57BL/6NJ-Utp4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263848	M	MP:0000575	increased foot pad pigmentation	Vangl1<tm1e(KOMP)Wtsi>/Vangl1<tm1e(KOMP)Wtsi>	C57BL/6N-Vangl1<tm1e(KOMP)Wtsi>/Wtsi	N	25340873
MGI:6263848	M	MP:0000574	abnormal foot pad morphology	Vangl1<tm1e(KOMP)Wtsi>/Vangl1<tm1e(KOMP)Wtsi>	C57BL/6N-Vangl1<tm1e(KOMP)Wtsi>/Wtsi	N	25340873
MGI:6263851	F	MP:0001415	increased exploration in new environment	Vgf<em1(IMPC)H>/Vgf<em1(IMPC)H>	C57BL/6NTac-Vgf<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263851	F	MP:0010088	decreased circulating fructosamine level	Vgf<em1(IMPC)H>/Vgf<em1(IMPC)H>	C57BL/6NTac-Vgf<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263851	M	MP:0004953	decreased spleen weight	Vgf<em1(IMPC)H>/Vgf<em1(IMPC)H>	C57BL/6NTac-Vgf<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263851	M	MP:0010052	increased grip strength	Vgf<em1(IMPC)H>/Vgf<em1(IMPC)H>	C57BL/6NTac-Vgf<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263851	F	MP:0005568	increased circulating total protein level	Vgf<em1(IMPC)H>/Vgf<em1(IMPC)H>	C57BL/6NTac-Vgf<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263851	F	MP:0001513	limb grasping	Vgf<em1(IMPC)H>/Vgf<em1(IMPC)H>	C57BL/6NTac-Vgf<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263851	F	MP:0002764	short tibia	Vgf<em1(IMPC)H>/Vgf<em1(IMPC)H>	C57BL/6NTac-Vgf<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263851	M	MP:0001925	male infertility	Vgf<em1(IMPC)H>/Vgf<em1(IMPC)H>	C57BL/6NTac-Vgf<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263851	F	MP:0000745	tremors	Vgf<em1(IMPC)H>/Vgf<em1(IMPC)H>	C57BL/6NTac-Vgf<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263851	F	MP:0009142	decreased prepulse inhibition	Vgf<em1(IMPC)H>/Vgf<em1(IMPC)H>	C57BL/6NTac-Vgf<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263852	F	MP:0001402	decreased locomotor activity	Vgll4<tm1b(EUCOMM)Hmgu>/Vgll4<+>	C57BL/6N-Vgll4<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263852	F	MP:0011886	increased circulating lipase level	Vgll4<tm1b(EUCOMM)Hmgu>/Vgll4<+>	C57BL/6N-Vgll4<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263852	M	MP:0010123	increased bone mineral content	Vgll4<tm1b(EUCOMM)Hmgu>/Vgll4<+>	C57BL/6N-Vgll4<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263854	F	MP:0002546	mydriasis	Vopp1<em1(IMPC)J>/Vopp1<em1(IMPC)J>	C57BL/6NJ-Vopp1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263854	M	MP:0006243	impaired pupillary reflex	Vopp1<em1(IMPC)J>/Vopp1<em1(IMPC)J>	C57BL/6NJ-Vopp1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263856	M	MP:0000219	increased neutrophil cell number	Vps33a<em2(IMPC)Tcp>/Vps33a<+>	C57BL/6NCrl-Vps33a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263856	M	MP:0003068	enlarged kidney	Vps33a<em2(IMPC)Tcp>/Vps33a<+>	C57BL/6NCrl-Vps33a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263856	M	MP:0002764	short tibia	Vps33a<em2(IMPC)Tcp>/Vps33a<+>	C57BL/6NCrl-Vps33a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263856	M	MP:0004952	increased spleen weight	Vps33a<em2(IMPC)Tcp>/Vps33a<+>	C57BL/6NCrl-Vps33a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263856	M	MP:0002833	increased heart weight	Vps33a<em2(IMPC)Tcp>/Vps33a<+>	C57BL/6NCrl-Vps33a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263856	M	MP:0005016	decreased lymphocyte cell number	Vps33a<em2(IMPC)Tcp>/Vps33a<+>	C57BL/6NCrl-Vps33a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263856	M	MP:0000157	abnormal sternum morphology	Vps33a<em2(IMPC)Tcp>/Vps33a<+>	C57BL/6NCrl-Vps33a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263856	M	MP:0010067	increased red blood cell distribution width	Vps33a<em2(IMPC)Tcp>/Vps33a<+>	C57BL/6NCrl-Vps33a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263856	M	MP:0011874	enlarged urinary bladder	Vps33a<em2(IMPC)Tcp>/Vps33a<+>	C57BL/6NCrl-Vps33a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263859	F	MP:0011960	abnormal eye anterior chamber depth	Vps9d1<tm1b(KOMP)Wtsi>/Vps9d1<tm1b(KOMP)Wtsi>	C57BL/6N-Vps9d1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263860	M	MP:0002941	increased circulating alanine transaminase level	Vrk1<em1(IMPC)Mbp>/Vrk1<+>	C57BL/6N-Vrk1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6263862	F	MP:0001944	abnormal pancreas morphology	Vrk3<em1(IMPC)Mbp>/Vrk3<em1(IMPC)Mbp>	C57BL/6NCrl-Vrk3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263862	F	MP:0000691	enlarged spleen	Vrk3<em1(IMPC)Mbp>/Vrk3<em1(IMPC)Mbp>	C57BL/6NCrl-Vrk3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263862	F	MP:0000689	abnormal spleen morphology	Vrk3<em1(IMPC)Mbp>/Vrk3<em1(IMPC)Mbp>	C57BL/6NCrl-Vrk3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263862	F	MP:0002060	abnormal skin morphology	Vrk3<em1(IMPC)Mbp>/Vrk3<em1(IMPC)Mbp>	C57BL/6NCrl-Vrk3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263862	F	MP:0002135	abnormal kidney morphology	Vrk3<em1(IMPC)Mbp>/Vrk3<em1(IMPC)Mbp>	C57BL/6NCrl-Vrk3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263862	M	MP:0002092	abnormal eye morphology	Vrk3<em1(IMPC)Mbp>/Vrk3<em1(IMPC)Mbp>	C57BL/6NCrl-Vrk3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263862	F	MP:0001192	scaly skin	Vrk3<em1(IMPC)Mbp>/Vrk3<em1(IMPC)Mbp>	C57BL/6NCrl-Vrk3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263862	M	MP:0000598	abnormal liver morphology	Vrk3<em1(IMPC)Mbp>/Vrk3<em1(IMPC)Mbp>	C57BL/6NCrl-Vrk3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263862	F	MP:0003068	enlarged kidney	Vrk3<em1(IMPC)Mbp>/Vrk3<em1(IMPC)Mbp>	C57BL/6NCrl-Vrk3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263863	M	MP:0000218	increased leukocyte cell number	Vsig10<em1(IMPC)Wtsi>/Vsig10<em1(IMPC)Wtsi>	C57BL/6N-Vsig10<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263865	F	MP:0013025	increased Ly6C low monocyte number	Wac<tm2b(EUCOMM)Wtsi>/Wac<+>	C57BL/6N-Wac<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263865	F	MP:0000220	increased monocyte cell number	Wac<tm2b(EUCOMM)Wtsi>/Wac<+>	C57BL/6N-Wac<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263865	M	MP:0008805	decreased circulating amylase level	Wac<tm2b(EUCOMM)Wtsi>/Wac<+>	C57BL/6N-Wac<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263865	M	MP:0002644	decreased circulating triglyceride level	Wac<tm2b(EUCOMM)Wtsi>/Wac<+>	C57BL/6N-Wac<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263865	F	MP:0004613	fusion of vertebral arches	Wac<tm2b(EUCOMM)Wtsi>/Wac<+>	C57BL/6N-Wac<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263865	M	MP:0002599	increased mean platelet volume	Wac<tm2b(EUCOMM)Wtsi>/Wac<+>	C57BL/6N-Wac<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263865	M	MP:0005012	decreased eosinophil cell number	Wac<tm2b(EUCOMM)Wtsi>/Wac<+>	C57BL/6N-Wac<tm2b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263871	F	MP:0002092	abnormal eye morphology	Washc3<tm1.1(KOMP)Vlcg>/Washc3<+>	C57BL/6N-Washc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263873	F	MP:0000208	decreased hematocrit	Wdfy4<em1(IMPC)J>/Wdfy4<em1(IMPC)J>	C57BL/6NJ-Wdfy4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263873	F	MP:0002875	decreased erythrocyte cell number	Wdfy4<em1(IMPC)J>/Wdfy4<em1(IMPC)J>	C57BL/6NJ-Wdfy4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263874	M	MP:0005292	improved glucose tolerance	Wdr11<em1(IMPC)Mbp>/Wdr11<+>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263874	M	MP:0001417	decreased exploration in new environment	Wdr11<em1(IMPC)Mbp>/Wdr11<+>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263874	M	MP:0003642	absent seminal vesicle	Wdr11<em1(IMPC)Mbp>/Wdr11<+>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263874	M	MP:0002135	abnormal kidney morphology	Wdr11<em1(IMPC)Mbp>/Wdr11<+>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263874	M	MP:0000955	abnormal spinal cord morphology	Wdr11<em1(IMPC)Mbp>/Wdr11<+>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263874	M	MP:0011999	abnormal tail length	Wdr11<em1(IMPC)Mbp>/Wdr11<+>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263874	F	MP:0002060	abnormal skin morphology	Wdr11<em1(IMPC)Mbp>/Wdr11<+>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263874	M	MP:0000274	enlarged heart	Wdr11<em1(IMPC)Mbp>/Wdr11<+>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263874	M	MP:0002997	enlarged seminal vesicle	Wdr11<em1(IMPC)Mbp>/Wdr11<+>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263874	F	MP:0002188	small heart	Wdr11<em1(IMPC)Mbp>/Wdr11<+>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263874	M	MP:0003068	enlarged kidney	Wdr11<em1(IMPC)Mbp>/Wdr11<+>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263875	M	MP:0003642	absent seminal vesicle	Wdr11<em1(IMPC)Mbp>/Wdr11<em1(IMPC)Mbp>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263875	F	MP:0002060	abnormal skin morphology	Wdr11<em1(IMPC)Mbp>/Wdr11<em1(IMPC)Mbp>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263875	F	MP:0002092	abnormal eye morphology	Wdr11<em1(IMPC)Mbp>/Wdr11<em1(IMPC)Mbp>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263875	M	MP:0002997	enlarged seminal vesicle	Wdr11<em1(IMPC)Mbp>/Wdr11<em1(IMPC)Mbp>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263875	M	MP:0005313	absent adrenal gland	Wdr11<em1(IMPC)Mbp>/Wdr11<em1(IMPC)Mbp>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263875	F	MP:0001120	abnormal uterus morphology	Wdr11<em1(IMPC)Mbp>/Wdr11<em1(IMPC)Mbp>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263875	F	MP:0000266	abnormal heart morphology	Wdr11<em1(IMPC)Mbp>/Wdr11<em1(IMPC)Mbp>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263875	F	MP:0002188	small heart	Wdr11<em1(IMPC)Mbp>/Wdr11<em1(IMPC)Mbp>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263875	M	MP:0000598	abnormal liver morphology	Wdr11<em1(IMPC)Mbp>/Wdr11<em1(IMPC)Mbp>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263875	M	MP:0001925	male infertility	Wdr11<em1(IMPC)Mbp>/Wdr11<em1(IMPC)Mbp>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263875	F	MP:0009709	hydrometra	Wdr11<em1(IMPC)Mbp>/Wdr11<em1(IMPC)Mbp>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263875	F	MP:0001293	anophthalmia	Wdr11<em1(IMPC)Mbp>/Wdr11<em1(IMPC)Mbp>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263875	F	MP:0010067	increased red blood cell distribution width	Wdr11<em1(IMPC)Mbp>/Wdr11<em1(IMPC)Mbp>	C57BL/6NCrl-Wdr11<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263878	M	MP:0001556	increased circulating HDL cholesterol level	Wdr45<em1(IMPC)J>/Y	C57BL/6NJ-Wdr45<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263878	M	MP:0001486	abnormal startle reflex	Wdr45<em1(IMPC)J>/Y	C57BL/6NJ-Wdr45<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263878	M	MP:0002833	increased heart weight	Wdr45<em1(IMPC)J>/Y	C57BL/6NJ-Wdr45<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263878	M	MP:0004738	abnormal auditory brainstem response	Wdr45<em1(IMPC)J>/Y	C57BL/6NJ-Wdr45<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263878	M	MP:0003795	abnormal bone structure	Wdr45<em1(IMPC)J>/Y	C57BL/6NJ-Wdr45<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263878	M	MP:0001399	hyperactivity	Wdr45<em1(IMPC)J>/Y	C57BL/6NJ-Wdr45<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263879	F	MP:0000063	decreased bone mineral density	Wdr45<em1(IMPC)J>/Wdr45<em1(IMPC)J>	C57BL/6NJ-Wdr45<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263879	F	MP:0002968	increased circulating alkaline phosphatase level	Wdr45<em1(IMPC)J>/Wdr45<em1(IMPC)J>	C57BL/6NJ-Wdr45<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263879	F	MP:0001399	hyperactivity	Wdr45<em1(IMPC)J>/Wdr45<em1(IMPC)J>	C57BL/6NJ-Wdr45<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263879	F	MP:0010124	decreased bone mineral content	Wdr45<em1(IMPC)J>/Wdr45<em1(IMPC)J>	C57BL/6NJ-Wdr45<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263879	F	MP:0001415	increased exploration in new environment	Wdr45<em1(IMPC)J>/Wdr45<em1(IMPC)J>	C57BL/6NJ-Wdr45<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263880	M	MP:0001147	small testis	Wdr62<em1(IMPC)Tcp>/Wdr62<em1(IMPC)Tcp>	C57BL/6NCrl-Wdr62<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263880	M	MP:0001157	small seminal vesicle	Wdr62<em1(IMPC)Tcp>/Wdr62<em1(IMPC)Tcp>	C57BL/6NCrl-Wdr62<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263880	M	MP:0001925	male infertility	Wdr62<em1(IMPC)Tcp>/Wdr62<em1(IMPC)Tcp>	C57BL/6NCrl-Wdr62<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263880	M	MP:0000702	enlarged lymph nodes	Wdr62<em1(IMPC)Tcp>/Wdr62<em1(IMPC)Tcp>	C57BL/6NCrl-Wdr62<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263880	F	MP:0001297	microphthalmia	Wdr62<em1(IMPC)Tcp>/Wdr62<em1(IMPC)Tcp>	C57BL/6NCrl-Wdr62<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263880	F	MP:0002989	small kidney	Wdr62<em1(IMPC)Tcp>/Wdr62<em1(IMPC)Tcp>	C57BL/6NCrl-Wdr62<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263880	M	MP:0009142	decreased prepulse inhibition	Wdr62<em1(IMPC)Tcp>/Wdr62<em1(IMPC)Tcp>	C57BL/6NCrl-Wdr62<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263880	F	MP:0005633	increased circulating sodium level	Wdr62<em1(IMPC)Tcp>/Wdr62<em1(IMPC)Tcp>	C57BL/6NCrl-Wdr62<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263882	M	MP:0002591	decreased mean corpuscular volume	Ntaq1<tm1.1(KOMP)Vlcg>/Ntaq1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ntaq1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263882	M	MP:0002941	increased circulating alanine transaminase level	Ntaq1<tm1.1(KOMP)Vlcg>/Ntaq1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ntaq1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263882	M	MP:0005562	decreased mean corpuscular hemoglobin	Ntaq1<tm1.1(KOMP)Vlcg>/Ntaq1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ntaq1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263882	M	MP:0000218	increased leukocyte cell number	Ntaq1<tm1.1(KOMP)Vlcg>/Ntaq1<tm1.1(KOMP)Vlcg>	C57BL/6N-Ntaq1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263883	M	MP:0000274	enlarged heart	Wfdc2<em1(IMPC)H>/Wfdc2<+>	C57BL/6NTac-Wfdc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263883	F	MP:0005012	decreased eosinophil cell number	Wfdc2<em1(IMPC)H>/Wfdc2<+>	C57BL/6NTac-Wfdc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263883	M	MP:0008806	increased circulating amylase level	Wfdc2<em1(IMPC)H>/Wfdc2<+>	C57BL/6NTac-Wfdc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6263885	F	MP:0001120	abnormal uterus morphology	Wnt11<tm1.1(KOMP)Vlcg>/Wnt11<tm1.1(KOMP)Vlcg>	C57BL/6N-Wnt11<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263885	F	MP:0009709	hydrometra	Wnt11<tm1.1(KOMP)Vlcg>/Wnt11<tm1.1(KOMP)Vlcg>	C57BL/6N-Wnt11<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263885	M	MP:0000266	abnormal heart morphology	Wnt11<tm1.1(KOMP)Vlcg>/Wnt11<tm1.1(KOMP)Vlcg>	C57BL/6N-Wnt11<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263885	M	MP:0001146	abnormal testis morphology	Wnt11<tm1.1(KOMP)Vlcg>/Wnt11<tm1.1(KOMP)Vlcg>	C57BL/6N-Wnt11<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263885	M	MP:0000274	enlarged heart	Wnt11<tm1.1(KOMP)Vlcg>/Wnt11<tm1.1(KOMP)Vlcg>	C57BL/6N-Wnt11<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263885	F	MP:0005565	increased blood urea nitrogen level	Wnt11<tm1.1(KOMP)Vlcg>/Wnt11<tm1.1(KOMP)Vlcg>	C57BL/6N-Wnt11<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263885	M	MP:0001147	small testis	Wnt11<tm1.1(KOMP)Vlcg>/Wnt11<tm1.1(KOMP)Vlcg>	C57BL/6N-Wnt11<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263886	M	MP:0005178	increased circulating cholesterol level	Wnt1<tm1b(EUCOMM)Wtsi>/Wnt1<+>	C57BL/6N-Wnt1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263887	M	MP:0011100	preweaning lethality, complete penetrance	Wnt1<tm1b(EUCOMM)Wtsi>/Wnt1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Wnt1<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263888	F	MP:0001289	persistence of hyaloid vascular system	Wnt2b<tm1b(EUCOMM)Wtsi>/Wnt2b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Wnt2b<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263888	M	MP:0000691	enlarged spleen	Wnt2b<tm1b(EUCOMM)Wtsi>/Wnt2b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Wnt2b<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263888	F	MP:0000692	small spleen	Wnt2b<tm1b(EUCOMM)Wtsi>/Wnt2b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Wnt2b<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263888	M	MP:0002135	abnormal kidney morphology	Wnt2b<tm1b(EUCOMM)Wtsi>/Wnt2b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Wnt2b<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263888	M	MP:0003068	enlarged kidney	Wnt2b<tm1b(EUCOMM)Wtsi>/Wnt2b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Wnt2b<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263889	F	MP:0005554	decreased circulating creatinine level	Wscd2<em1(IMPC)J>/Wscd2<em1(IMPC)J>	C57BL/6NJ-Wscd2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263889	F	MP:0001399	hyperactivity	Wscd2<em1(IMPC)J>/Wscd2<em1(IMPC)J>	C57BL/6NJ-Wscd2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263889	F	MP:0020870	decreased thigmotaxis	Wscd2<em1(IMPC)J>/Wscd2<em1(IMPC)J>	C57BL/6NJ-Wscd2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263890	M	MP:0013279	increased fasting circulating glucose level	Xkr5<tm1b(KOMP)Mbp>/Xkr5<tm1b(KOMP)Mbp>	C57BL/6N-Xkr5<tm1b(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:6263893	M	MP:0005178	increased circulating cholesterol level	Yae1d1<tm1b(EUCOMM)Hmgu>/Yae1d1<+>	C57BL/6N-Yae1d1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263893	F	MP:0011886	increased circulating lipase level	Yae1d1<tm1b(EUCOMM)Hmgu>/Yae1d1<+>	C57BL/6N-Yae1d1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263893	F	MP:0001304	cataract	Yae1d1<tm1b(EUCOMM)Hmgu>/Yae1d1<+>	C57BL/6N-Yae1d1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263893	M	MP:0009142	decreased prepulse inhibition	Yae1d1<tm1b(EUCOMM)Hmgu>/Yae1d1<+>	C57BL/6N-Yae1d1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263895	M	MP:0010024	increased total body fat amount	Ylpm1<tm1b(KOMP)Wtsi>/Ylpm1<+>	C57BL/6N-Ylpm1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6263897	F	MP:0001289	persistence of hyaloid vascular system	Zbtb43<tm1b(KOMP)Mbp>/Zbtb43<+>	C57BL/6N-Zbtb43<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263897	F	MP:0005560	decreased circulating glucose level	Zbtb43<tm1b(KOMP)Mbp>/Zbtb43<+>	C57BL/6N-Zbtb43<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263898	M	MP:0001566	increased circulating phosphate level	Zbtb43<tm1b(KOMP)Mbp>/Zbtb43<tm1b(KOMP)Mbp>	C57BL/6N-Zbtb43<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263898	M	MP:0002590	increased mean corpuscular volume	Zbtb43<tm1b(KOMP)Mbp>/Zbtb43<tm1b(KOMP)Mbp>	C57BL/6N-Zbtb43<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263898	M	MP:0003960	increased lean body mass	Zbtb43<tm1b(KOMP)Mbp>/Zbtb43<tm1b(KOMP)Mbp>	C57BL/6N-Zbtb43<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263898	M	MP:0006243	impaired pupillary reflex	Zbtb43<tm1b(KOMP)Mbp>/Zbtb43<tm1b(KOMP)Mbp>	C57BL/6N-Zbtb43<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263898	M	MP:0005560	decreased circulating glucose level	Zbtb43<tm1b(KOMP)Mbp>/Zbtb43<tm1b(KOMP)Mbp>	C57BL/6N-Zbtb43<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263898	M	MP:0005343	increased circulating aspartate transaminase level	Zbtb43<tm1b(KOMP)Mbp>/Zbtb43<tm1b(KOMP)Mbp>	C57BL/6N-Zbtb43<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263898	M	MP:0002941	increased circulating alanine transaminase level	Zbtb43<tm1b(KOMP)Mbp>/Zbtb43<tm1b(KOMP)Mbp>	C57BL/6N-Zbtb43<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263898	M	MP:0005419	decreased circulating serum albumin level	Zbtb43<tm1b(KOMP)Mbp>/Zbtb43<tm1b(KOMP)Mbp>	C57BL/6N-Zbtb43<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263899	F	MP:0000274	enlarged heart	Zbtb46<tm1.1(KOMP)Vlcg>/Zbtb46<+>	C57BL/6N-Zbtb46<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263899	M	MP:0001146	abnormal testis morphology	Zbtb46<tm1.1(KOMP)Vlcg>/Zbtb46<+>	C57BL/6N-Zbtb46<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263899	M	MP:0001147	small testis	Zbtb46<tm1.1(KOMP)Vlcg>/Zbtb46<+>	C57BL/6N-Zbtb46<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263899	F	MP:0000266	abnormal heart morphology	Zbtb46<tm1.1(KOMP)Vlcg>/Zbtb46<+>	C57BL/6N-Zbtb46<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263900	F	MP:0009709	hydrometra	Zbtb48<em1(IMPC)Mbp>/Zbtb48<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb48<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263900	F	MP:0010123	increased bone mineral content	Zbtb48<em1(IMPC)Mbp>/Zbtb48<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb48<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263900	M	MP:0010024	increased total body fat amount	Zbtb48<em1(IMPC)Mbp>/Zbtb48<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb48<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263900	F	MP:0001120	abnormal uterus morphology	Zbtb48<em1(IMPC)Mbp>/Zbtb48<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb48<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263900	F	MP:0003795	abnormal bone structure	Zbtb48<em1(IMPC)Mbp>/Zbtb48<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb48<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263900	F	MP:0001417	decreased exploration in new environment	Zbtb48<em1(IMPC)Mbp>/Zbtb48<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb48<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263900	M	MP:0005293	impaired glucose tolerance	Zbtb48<em1(IMPC)Mbp>/Zbtb48<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb48<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6263902	M	MP:0009456	impaired cued conditioning behavior	Zc3h12b<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Zc3h12b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263903	F	MP:0001126	abnormal ovary morphology	Zc3h12b<em1(IMPC)Tcp>/Zc3h12b<em1(IMPC)Tcp>	C57BL/6NCrl-Zc3h12b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263903	F	MP:0000702	enlarged lymph nodes	Zc3h12b<em1(IMPC)Tcp>/Zc3h12b<em1(IMPC)Tcp>	C57BL/6NCrl-Zc3h12b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263903	F	MP:0001297	microphthalmia	Zc3h12b<em1(IMPC)Tcp>/Zc3h12b<em1(IMPC)Tcp>	C57BL/6NCrl-Zc3h12b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263903	F	MP:0002637	small uterus	Zc3h12b<em1(IMPC)Tcp>/Zc3h12b<em1(IMPC)Tcp>	C57BL/6NCrl-Zc3h12b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263903	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Zc3h12b<em1(IMPC)Tcp>/Zc3h12b<em1(IMPC)Tcp>	C57BL/6NCrl-Zc3h12b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6263904	F	MP:0001312	abnormal cornea morphology	Zc3h14<tm1a(KOMP)Wtsi>/Zc3h14<tm1a(KOMP)Wtsi>	C57BL/6N-Zc3h14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263906	F	MP:0002092	abnormal eye morphology	Zc3hav1l<tm1b(EUCOMM)Wtsi>/Zc3hav1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zc3hav1l<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263906	F	MP:0000598	abnormal liver morphology	Zc3hav1l<tm1b(EUCOMM)Wtsi>/Zc3hav1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zc3hav1l<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6263907	M	MP:0002152	abnormal brain morphology	Zdhhc3<tm1.1(KOMP)Vlcg>/Zdhhc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Zdhhc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263907	M	MP:0001891	hydrocephaly	Zdhhc3<tm1.1(KOMP)Vlcg>/Zdhhc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Zdhhc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6263908	F	MP:0010052	increased grip strength	Zfp202<em1(IMPC)J>/Zfp202<em1(IMPC)J>	C57BL/6NJ-Zfp202<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263908	M	MP:0005178	increased circulating cholesterol level	Zfp202<em1(IMPC)J>/Zfp202<em1(IMPC)J>	C57BL/6NJ-Zfp202<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263908	M	MP:0010124	decreased bone mineral content	Zfp202<em1(IMPC)J>/Zfp202<em1(IMPC)J>	C57BL/6NJ-Zfp202<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263908	M	MP:0003961	decreased lean body mass	Zfp202<em1(IMPC)J>/Zfp202<em1(IMPC)J>	C57BL/6NJ-Zfp202<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263908	M	MP:0010024	increased total body fat amount	Zfp202<em1(IMPC)J>/Zfp202<em1(IMPC)J>	C57BL/6NJ-Zfp202<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263909	M	MP:0005599	increased cardiac muscle contractility	Zfp235<tm1b(KOMP)Wtsi>/Zfp235<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp235<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263909	F	MP:0010052	increased grip strength	Zfp235<tm1b(KOMP)Wtsi>/Zfp235<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp235<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263910	F	MP:0002546	mydriasis	Zfp329<em1(IMPC)J>/Zfp329<em1(IMPC)J>	C57BL/6NJ-Zfp329<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263910	M	MP:0008259	abnormal optic disk morphology	Zfp329<em1(IMPC)J>/Zfp329<em1(IMPC)J>	C57BL/6NJ-Zfp329<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263910	F	MP:0010053	decreased grip strength	Zfp329<em1(IMPC)J>/Zfp329<em1(IMPC)J>	C57BL/6NJ-Zfp329<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263911	F	MP:0005344	increased circulating bilirubin level	Zfp334<tm1.1(KOMP)Vlcg>/Zfp334<tm1.1(KOMP)Vlcg>	C57BL/6N-Zfp334<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263911	F	MP:0001399	hyperactivity	Zfp334<tm1.1(KOMP)Vlcg>/Zfp334<tm1.1(KOMP)Vlcg>	C57BL/6N-Zfp334<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6263912	M	MP:0005633	increased circulating sodium level	Zfp341<tm1a(KOMP)Wtsi>/Zfp341<tm1a(KOMP)Wtsi>	C57BL/6N-Zfp341<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263912	M	MP:0010123	increased bone mineral content	Zfp341<tm1a(KOMP)Wtsi>/Zfp341<tm1a(KOMP)Wtsi>	C57BL/6N-Zfp341<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263913	M	MP:0002574	increased vertical activity	Zfp407<em1(IMPC)J>/Zfp407<+>	C57BL/6NJ-Zfp407<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263915	M	MP:0005013	increased lymphocyte cell number	Zfp420<tm1b(EUCOMM)Hmgu>/Zfp420<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp420<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6263916	M	MP:0001488	increased startle reflex	Zfp422<em1(IMPC)J>/Zfp422<em1(IMPC)J>	C57BL/6NJ-Zfp422<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263916	M	MP:0001486	abnormal startle reflex	Zfp422<em1(IMPC)J>/Zfp422<em1(IMPC)J>	C57BL/6NJ-Zfp422<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263916	F	MP:0005292	improved glucose tolerance	Zfp422<em1(IMPC)J>/Zfp422<em1(IMPC)J>	C57BL/6NJ-Zfp422<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263917	M	MP:0011965	decreased total retina thickness	Zfp445<tm1b(EUCOMM)Hmgu>/Zfp445<+>	C57BL/6N-Zfp445<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263917	M	MP:0010053	decreased grip strength	Zfp445<tm1b(EUCOMM)Hmgu>/Zfp445<+>	C57BL/6N-Zfp445<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263918	F	MP:0010067	increased red blood cell distribution width	Zfp445<tm1b(EUCOMM)Hmgu>/Zfp445<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp445<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263918	F	MP:0000194	increased circulating calcium level	Zfp445<tm1b(EUCOMM)Hmgu>/Zfp445<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp445<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263918	F	MP:0011965	decreased total retina thickness	Zfp445<tm1b(EUCOMM)Hmgu>/Zfp445<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp445<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263918	F	MP:0002152	abnormal brain morphology	Zfp445<tm1b(EUCOMM)Hmgu>/Zfp445<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp445<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263920	M	MP:0005016	decreased lymphocyte cell number	Zfp595<tm1b(KOMP)Wtsi>/Zfp595<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp595<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263920	M	MP:0005012	decreased eosinophil cell number	Zfp595<tm1b(KOMP)Wtsi>/Zfp595<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp595<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263920	M	MP:0000221	decreased leukocyte cell number	Zfp595<tm1b(KOMP)Wtsi>/Zfp595<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp595<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6263921	M	MP:0020870	decreased thigmotaxis	Zfp60<tm1b(KOMP)Mbp>/Zfp60<+>	C57BL/6N-Zfp60<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6263922	F	MP:0005554	decreased circulating creatinine level	Zfp612<em1(IMPC)J>/Zfp612<em1(IMPC)J>	C57BL/6NJ-Zfp612<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263922	M	MP:0002591	decreased mean corpuscular volume	Zfp612<em1(IMPC)J>/Zfp612<em1(IMPC)J>	C57BL/6NJ-Zfp612<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263923	F	MP:0005553	increased circulating creatinine level	Zfp61<tm1b(EUCOMM)Hmgu>/Zfp61<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp61<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263923	F	MP:0009476	enlarged cecum	Zfp61<tm1b(EUCOMM)Hmgu>/Zfp61<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp61<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6263924	F	MP:0002591	decreased mean corpuscular volume	Zfp641<em1(IMPC)J>/Zfp641<em1(IMPC)J>	C57BL/6NJ-Zfp641<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263924	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Zfp641<em1(IMPC)J>/Zfp641<em1(IMPC)J>	C57BL/6NJ-Zfp641<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263924	F	MP:0005564	increased hemoglobin content	Zfp641<em1(IMPC)J>/Zfp641<em1(IMPC)J>	C57BL/6NJ-Zfp641<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263925	M	MP:0005554	decreased circulating creatinine level	Zfp692<em1(IMPC)J>/Zfp692<em1(IMPC)J>	C57BL/6NJ-Zfp692<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263926	M	MP:0001523	impaired righting response	Zfp706<em1(IMPC)J>/Zfp706<+>	C57BL/6NJ-Zfp706<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263926	M	MP:0001513	limb grasping	Zfp706<em1(IMPC)J>/Zfp706<+>	C57BL/6NJ-Zfp706<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263926	M	MP:0002075	abnormal coat/hair pigmentation	Zfp706<em1(IMPC)J>/Zfp706<+>	C57BL/6NJ-Zfp706<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263929	M	MP:0003443	increased circulating glycerol level	Zfp763<em1(IMPC)Wtsi>/Zfp763<em1(IMPC)Wtsi>	C57BL/6N-Zfp763<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6263933	M	MP:0010024	increased total body fat amount	Zfp92<em1(IMPC)J>/Y	C57BL/6NJ-Zfp92<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263933	M	MP:0003961	decreased lean body mass	Zfp92<em1(IMPC)J>/Y	C57BL/6NJ-Zfp92<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263933	M	MP:0010124	decreased bone mineral content	Zfp92<em1(IMPC)J>/Y	C57BL/6NJ-Zfp92<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263934	F	MP:0001304	cataract	Zfp92<em1(IMPC)J>/Zfp92<em1(IMPC)J>	C57BL/6NJ-Zfp92<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6263935	F	MP:0005477	increased circulating thyroxine level	Zmynd11<em1(IMPC)Wtsi>/Zmynd11<+>	C57BL/6N-Zmynd11<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6263938	F	MP:0010053	decreased grip strength	Zscan12<em1(IMPC)J>/Zscan12<em1(IMPC)J>	C57BL/6NJ-Zscan12<em1(IMPC)J>/J	N	MGI:5576271
MGI:6263939	F	MP:0001926	female infertility	Zscan21<tm2b(EUCOMM)Wtsi>/Zscan21<tm2b(EUCOMM)Wtsi>	C57BL/6N-Zscan21<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6263939	M	MP:0001925	male infertility	Zscan21<tm2b(EUCOMM)Wtsi>/Zscan21<tm2b(EUCOMM)Wtsi>	C57BL/6N-Zscan21<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6267048	F	MP:0013624	decreased femur compact bone thickness	Pls3<tm1d(EUCOMM)Wtsi>/Pls3<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267048	F	MP:0010968	decreased compact bone area	Pls3<tm1d(EUCOMM)Wtsi>/Pls3<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267048	F	MP:0010869	decreased bone trabecula number	Pls3<tm1d(EUCOMM)Wtsi>/Pls3<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267048	F	MP:0004992	increased bone resorption	Pls3<tm1d(EUCOMM)Wtsi>/Pls3<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267048	F	MP:0010876	decreased bone volume	Pls3<tm1d(EUCOMM)Wtsi>/Pls3<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267048	F	MP:0001533	abnormal skeleton physiology	Pls3<tm1d(EUCOMM)Wtsi>/Pls3<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267048	F	MP:0000066	osteoporosis	Pls3<tm1d(EUCOMM)Wtsi>/Pls3<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267048	F	MP:0013630	increased bone trabecular spacing	Pls3<tm1d(EUCOMM)Wtsi>/Pls3<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267048	F	MP:0005390	skeleton phenotype	Pls3<tm1d(EUCOMM)Wtsi>/Pls3<tm1d(EUCOMM)Wtsi>	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	Y	30204862
MGI:6267049	M	MP:0000066	osteoporosis	Pls3<tm1d(EUCOMM)Wtsi>/Y	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267049	M	MP:0004992	increased bone resorption	Pls3<tm1d(EUCOMM)Wtsi>/Y	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267049	M	MP:0010968	decreased compact bone area	Pls3<tm1d(EUCOMM)Wtsi>/Y	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267049	M	MP:0005390	skeleton phenotype	Pls3<tm1d(EUCOMM)Wtsi>/Y	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	Y	30204862
MGI:6267049	M	MP:0010869	decreased bone trabecula number	Pls3<tm1d(EUCOMM)Wtsi>/Y	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267049	M	MP:0004991	decreased bone strength	Pls3<tm1d(EUCOMM)Wtsi>/Y	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267049	M	MP:0013639	decreased bone stiffness	Pls3<tm1d(EUCOMM)Wtsi>/Y	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267049	M	MP:0013630	increased bone trabecular spacing	Pls3<tm1d(EUCOMM)Wtsi>/Y	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267049	M	MP:0013624	decreased femur compact bone thickness	Pls3<tm1d(EUCOMM)Wtsi>/Y	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6267049	M	MP:0001533	abnormal skeleton physiology	Pls3<tm1d(EUCOMM)Wtsi>/Y	involves: BALB/cJ * C57BL/6N * C57BL/6NTac * SJL	N	30204862
MGI:6269453	F	MP:0010025	decreased total body fat amount	Npr3<kylb>/Npr3<kylb>	involves: BALB/c * C57BL/6J	N	27959934
MGI:6269453	F	MP:0002968	increased circulating alkaline phosphatase level	Npr3<kylb>/Npr3<kylb>	involves: BALB/c * C57BL/6J	N	27959934
MGI:6270171	M	MP:0012574	decreased noradrenaline level	Tg(Camk2a-Polg*D181A)BTkato/0	C57BL/6J-Tg(Camk2a-Polg*D181A)BTkato	N	16619054
MGI:6270171	M	MP:0001905	abnormal dopamine level	Tg(Camk2a-Polg*D181A)BTkato/0	C57BL/6J-Tg(Camk2a-Polg*D181A)BTkato	N	16619054
MGI:6270171	M	MP:0011940	decreased food intake	Tg(Camk2a-Polg*D181A)BTkato/0	C57BL/6J-Tg(Camk2a-Polg*D181A)BTkato	N	16619054
MGI:6270171	M	MP:0001488	increased startle reflex	Tg(Camk2a-Polg*D181A)BTkato/0	C57BL/6J-Tg(Camk2a-Polg*D181A)BTkato	N	16619054
MGI:6270171	M	MP:0010070	decreased serotonin level	Tg(Camk2a-Polg*D181A)BTkato/0	C57BL/6J-Tg(Camk2a-Polg*D181A)BTkato	N	16619054
MGI:6270171	M	MP:0005386	behavior/neurological phenotype	Tg(Camk2a-Polg*D181A)BTkato/0	C57BL/6J-Tg(Camk2a-Polg*D181A)BTkato	Y	16619054
MGI:6270171	M	MP:0003459	increased fear-related response	Tg(Camk2a-Polg*D181A)BTkato/0	C57BL/6J-Tg(Camk2a-Polg*D181A)BTkato	N	16619054
MGI:6270368	F	MP:0008548	abnormal circulating interferon level	Trim13<tm1.1Jskg>/Trim13<tm1.1Jskg>	B6.129S7(Cg)-Trim13<tm1.1Jskg>	N	25008915
MGI:6270368	F	MP:0031039	decreased susceptibility to Picornaviridae infection induced morbidity/mortality	Trim13<tm1.1Jskg>/Trim13<tm1.1Jskg>	B6.129S7(Cg)-Trim13<tm1.1Jskg>	N	25008915
MGI:6270368	F	MP:0008576	decreased circulating interferon-beta level	Trim13<tm1.1Jskg>/Trim13<tm1.1Jskg>	B6.129S7(Cg)-Trim13<tm1.1Jskg>	N	25008915
MGI:6272000	F	MP:0009221	uterus adenomyosis	Klf11<tm1Czs>/Klf11<tm1Czs>	B6.129-Klf11<tm1Czs>	N	23555910
MGI:6272000	F	MP:0005165	increased susceptibility to injury	Klf11<tm1Czs>/Klf11<tm1Czs>	B6.129-Klf11<tm1Czs>	N	23555910
MGI:6272001	F	MP:0005389	reproductive system phenotype	Klf9<tm1Yfk>/Klf9<tm1Yfk>	B6.129P2-Klf9<tm1Yfk>/J	Y	23555910
MGI:6272327	M	MP:0008261	arrest of male meiosis	Eif4g3<repro8>/Eif4g3<repro8>	C3Fe.B6-Eif4g3<repro8>/Hand	N	29161344
MGI:6272787	F	MP:0009932	skin fibrosis	Aldh18a1<tm1a(KOMP)Wtsi>/Aldh18a1<+>	C57BL/6N-Aldh18a1<tm1a(KOMP)Wtsi>/Wtsi	N	25340873
MGI:6272787	F	MP:0004947	skin inflammation	Aldh18a1<tm1a(KOMP)Wtsi>/Aldh18a1<+>	C57BL/6N-Aldh18a1<tm1a(KOMP)Wtsi>/Wtsi	N	25340873
MGI:6272787	F	MP:0011156	abnormal hypodermis fat layer morphology	Aldh18a1<tm1a(KOMP)Wtsi>/Aldh18a1<+>	C57BL/6N-Aldh18a1<tm1a(KOMP)Wtsi>/Wtsi	N	25340873
MGI:6272789	F	MP:0008861	abnormal hair shedding	Farp2<tm1a(KOMP)Wtsi>/Farp2<tm1a(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Farp2<tm1a(KOMP)Wtsi>/Wtsi	N	25340873
MGI:6272789	F	MP:0000427	abnormal hair cycle	Farp2<tm1a(KOMP)Wtsi>/Farp2<tm1a(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Farp2<tm1a(KOMP)Wtsi>/Wtsi	N	25340873
MGI:6272791	F	MP:0008858	abnormal hair cycle anagen phase	Nf1<tm1a(KOMP)Wtsi>/Nf1<+>	B6Dnk;B6Brd;B6N-Tyr<c-Brd> Nf1<tm1a(KOMP)Wtsi>/Wtsi	N	25340873
MGI:6272793	F	MP:0008858	abnormal hair cycle anagen phase	Trpc4ap<tm1a(KOMP)Wtsi>/Trpc4ap<+>	C57BL/6N-Trpc4ap<tm1a(KOMP)Wtsi>/Wtsi	N	25340873
MGI:6272796	F	MP:0008858	abnormal hair cycle anagen phase	Nom1<tm1a(KOMP)Wtsi>/Nom1<+>	B6Brd;B6N-Tyr<c-Brd> Nom1<tm1a(KOMP)Wtsi>/Wtsi	N	25340873
MGI:6272808	F	MP:0011156	abnormal hypodermis fat layer morphology	Prmt3<tm1a(EUCOMM)Wtsi>/Prmt3<tm1a(EUCOMM)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Prmt3<tm1a(EUCOMM)Wtsi>/Wtsi	N	25340873
MGI:6272823	F	MP:0010679	abnormal arrector pilli muscle morphology	Rad18<tm1a(EUCOMM)Wtsi>/Rad18<tm1a(EUCOMM)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Rad18<tm1a(EUCOMM)Wtsi>/Wtsi	N	25340873
MGI:6272832	F	MP:0008861	abnormal hair shedding	Lrig1<tm1a(EUCOMM)Wtsi>/Lrig1<tm1a(EUCOMM)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Lrig1<tm1a(EUCOMM)Wtsi>/Wtsi	N	25340873
MGI:6272832	F	MP:0000427	abnormal hair cycle	Lrig1<tm1a(EUCOMM)Wtsi>/Lrig1<tm1a(EUCOMM)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Lrig1<tm1a(EUCOMM)Wtsi>/Wtsi	N	25340873
MGI:6273140	F	MP:0003413	hair follicle degeneration	Pfkl<tm1a(EUCOMM)Wtsi>/Pfkl<+>	B6Dnk;B6Brd;B6N-Tyr<c-Brd> Pfkl<tm1a(EUCOMM)Wtsi>/Wtsi	N	25340873
MGI:6273140	F	MP:0008859	abnormal hair cycle catagen phase	Pfkl<tm1a(EUCOMM)Wtsi>/Pfkl<+>	B6Dnk;B6Brd;B6N-Tyr<c-Brd> Pfkl<tm1a(EUCOMM)Wtsi>/Wtsi	N	25340873
MGI:6273149	M	MP:0000427	abnormal hair cycle	Myo5a<tm1e(KOMP)Wtsi>/Myo5a<tm1e(KOMP)Wtsi>	B6Brd;B6N-Tyr<c-Brd> Myo5a<tm1e(KOMP)Wtsi>/Wtsi	N	25340873
MGI:6273305	F	MP:0008861	abnormal hair shedding	Nsun2<tm1a(EUCOMM)Wtsi>/Nsun2<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Nsun2<tm1a(EUCOMM)Wtsi>/Wtsi	N	25340873
MGI:6273305	F	MP:0000427	abnormal hair cycle	Nsun2<tm1a(EUCOMM)Wtsi>/Nsun2<+>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Nsun2<tm1a(EUCOMM)Wtsi>/Wtsi	N	25340873
MGI:6273992	M	MP:0002687	oligozoospermia	Eqtn<tm1Gar>/Eqtn<tm1Gar>	involves: 129 * C57BL/6	N	24480441
MGI:6273992	M	MP:0000242	impaired fertilization	Eqtn<tm1Gar>/Eqtn<tm1Gar>	involves: 129 * C57BL/6	N	24480441
MGI:6273992	M	MP:0009647	decreased fertilization frequency	Eqtn<tm1Gar>/Eqtn<tm1Gar>	involves: 129 * C57BL/6	N	24480441
MGI:6273992	M	MP:0001922	reduced male fertility	Eqtn<tm1Gar>/Eqtn<tm1Gar>	involves: 129 * C57BL/6	N	24480441
MGI:6273992	M	MP:0004542	impaired acrosome reaction	Eqtn<tm1Gar>/Eqtn<tm1Gar>	involves: 129 * C57BL/6	N	24480441
MGI:6273992	M	MP:0001935	decreased litter size	Eqtn<tm1Gar>/Eqtn<tm1Gar>	involves: 129 * C57BL/6	N	24480441
MGI:6273993	M	MP:0002790	decreased circulating follicle stimulating hormone level	Tg(RP11-578M14)5Mkru/0	involves: FVB/N	N	29206867
MGI:6273993	F	MP:0002702	decreased circulating free fatty acids level	Tg(RP11-578M14)5Mkru/0	involves: FVB/N	N	29206867
MGI:6273993	M	MP:0005119	decreased circulating thyroid-stimulating hormone level	Tg(RP11-578M14)5Mkru/0	involves: FVB/N	N	29206867
MGI:6273993	M	MP:0005136	decreased growth hormone level	Tg(RP11-578M14)5Mkru/0	involves: FVB/N	N	29206867
MGI:6273993	M	MP:0002773	decreased circulating luteinizing hormone level	Tg(RP11-578M14)5Mkru/0	involves: FVB/N	N	29206867
MGI:6273993	M	MP:0011613	decreased circulating ghrelin level	Tg(RP11-578M14)5Mkru/0	involves: FVB/N	N	29206867
MGI:6273993	M	MP:0005138	decreased prolactin level	Tg(RP11-578M14)5Mkru/0	involves: FVB/N	N	29206867
MGI:6273993	M	MP:0005418	abnormal circulating hormone level	Tg(RP11-578M14)5Mkru/0	involves: FVB/N	N	29206867
MGI:6274231	M	MP:0008545	absent sperm flagellum	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0008892	abnormal sperm flagellum morphology	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0006380	abnormal spermatid morphology	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0009239	short sperm flagellum	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0009833	absent sperm mitochondrial sheath	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0031375	abnormal manchette disassembly	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0031373	abnormal manchette perinuclear ring morphology	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0031386	elongated manchette	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0020869	immotile sperm	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0001932	abnormal spermiogenesis	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0031356	abnormal outer dense fiber morphology	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0020550	multinucleated giant male germ cells	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0009231	detached acrosome	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0001925	male infertility	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0009838	abnormal sperm axoneme morphology	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0004182	abnormal spermiation	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0001156	abnormal spermatogenesis	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274231	M	MP:0009230	abnormal sperm head morphology	Katnal2<m1Anu>/Katnal2<m1Anu>	C57BL/6J-Katnal2<m1Anu>	N	29136647
MGI:6274235	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Katnal2<tm1a(EUCOMM)Wtsi>/Katnal2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Katnal2<tm1a(EUCOMM)Wtsi>	N	29136647
MGI:6274235	M	MP:0001925	male infertility	Katnal2<tm1a(EUCOMM)Wtsi>/Katnal2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Katnal2<tm1a(EUCOMM)Wtsi>	N	29136647
MGI:6274235	M	MP:0006380	abnormal spermatid morphology	Katnal2<tm1a(EUCOMM)Wtsi>/Katnal2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Katnal2<tm1a(EUCOMM)Wtsi>	N	29136647
MGI:6274235	M	MP:0001156	abnormal spermatogenesis	Katnal2<tm1a(EUCOMM)Wtsi>/Katnal2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Katnal2<tm1a(EUCOMM)Wtsi>	N	29136647
MGI:6274235	M	MP:0004182	abnormal spermiation	Katnal2<tm1a(EUCOMM)Wtsi>/Katnal2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Katnal2<tm1a(EUCOMM)Wtsi>	N	29136647
MGI:6274235	M	MP:0020550	multinucleated giant male germ cells	Katnal2<tm1a(EUCOMM)Wtsi>/Katnal2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Katnal2<tm1a(EUCOMM)Wtsi>	N	29136647
MGI:6274238	M	MP:0001925	male infertility	Katnal2<m1Anu>/Katnal2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29136647
MGI:6274238	M	MP:0006380	abnormal spermatid morphology	Katnal2<m1Anu>/Katnal2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29136647
MGI:6274238	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Katnal2<m1Anu>/Katnal2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29136647
MGI:6274238	M	MP:0020550	multinucleated giant male germ cells	Katnal2<m1Anu>/Katnal2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29136647
MGI:6274238	M	MP:0004182	abnormal spermiation	Katnal2<m1Anu>/Katnal2<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29136647
MGI:6274241	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Katnal2<tm1c(EUCOMM)Wtsi>/Katnal2<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29136647
MGI:6274241	M	MP:0031386	elongated manchette	Katnal2<tm1c(EUCOMM)Wtsi>/Katnal2<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29136647
MGI:6274241	M	MP:0004182	abnormal spermiation	Katnal2<tm1c(EUCOMM)Wtsi>/Katnal2<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29136647
MGI:6274241	M	MP:0020550	multinucleated giant male germ cells	Katnal2<tm1c(EUCOMM)Wtsi>/Katnal2<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29136647
MGI:6274241	M	MP:0008892	abnormal sperm flagellum morphology	Katnal2<tm1c(EUCOMM)Wtsi>/Katnal2<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29136647
MGI:6274241	M	MP:0001925	male infertility	Katnal2<tm1c(EUCOMM)Wtsi>/Katnal2<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29136647
MGI:6274241	M	MP:0006380	abnormal spermatid morphology	Katnal2<tm1c(EUCOMM)Wtsi>/Katnal2<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29136647
MGI:6274280	F	MP:0004924	abnormal behavior	Tg(Krt14-Rac1*G12V)#Mrnk/0	involves: CBA/CaJ	N	27294528
MGI:6274702	M	MP:0001360	abnormal social investigation	Scn1a<tm2.1Wac>/Scn1a<+>,Tg(I12b-cre)1Jlr/0	involves: 129X1/SvJ * C57BL/6J	N	22914087
MGI:6274702	M	MP:0001394	circling	Scn1a<tm2.1Wac>/Scn1a<+>,Tg(I12b-cre)1Jlr/0	involves: 129X1/SvJ * C57BL/6J	N	22914087
MGI:6274702	M	MP:0001363	increased anxiety-related response	Scn1a<tm2.1Wac>/Scn1a<+>,Tg(I12b-cre)1Jlr/0	involves: 129X1/SvJ * C57BL/6J	N	22914087
MGI:6274702	M	MP:0031391	increased locomotor activity	Scn1a<tm2.1Wac>/Scn1a<+>,Tg(I12b-cre)1Jlr/0	involves: 129X1/SvJ * C57BL/6J	N	22914087
MGI:6274702	M	MP:0002797	increased thigmotaxis	Scn1a<tm2.1Wac>/Scn1a<+>,Tg(I12b-cre)1Jlr/0	involves: 129X1/SvJ * C57BL/6J	N	22914087
MGI:6274702	M	MP:0014378	increased excitatory postsynaptic current frequency	Scn1a<tm2.1Wac>/Scn1a<+>,Tg(I12b-cre)1Jlr/0	involves: 129X1/SvJ * C57BL/6J	N	22914087
MGI:6274702	M	MP:0009454	impaired contextual conditioning behavior	Scn1a<tm2.1Wac>/Scn1a<+>,Tg(I12b-cre)1Jlr/0	involves: 129X1/SvJ * C57BL/6J	N	22914087
MGI:6274702	M	MP:0002945	abnormal inhibitory postsynaptic currents	Scn1a<tm2.1Wac>/Scn1a<+>,Tg(I12b-cre)1Jlr/0	involves: 129X1/SvJ * C57BL/6J	N	22914087
MGI:6274738	M	MP:0002702	decreased circulating free fatty acids level	Mir22<tm1Boet>/Mir22<tm1Boet>	B6.129S2-Mir22<tm1Boet>	N	28314781
MGI:6274738	M	MP:0009133	decreased white fat cell size	Mir22<tm1Boet>/Mir22<tm1Boet>	B6.129S2-Mir22<tm1Boet>	N	28314781
MGI:6274738	M	MP:0005668	decreased circulating leptin level	Mir22<tm1Boet>/Mir22<tm1Boet>	B6.129S2-Mir22<tm1Boet>	N	28314781
MGI:6274738	M	MP:0001783	decreased white adipose tissue amount	Mir22<tm1Boet>/Mir22<tm1Boet>	B6.129S2-Mir22<tm1Boet>	N	28314781
MGI:6274738	M	MP:0001262	decreased body weight	Mir22<tm1Boet>/Mir22<tm1Boet>	B6.129S2-Mir22<tm1Boet>	N	28314781
MGI:6275172	M	MP:0001158	abnormal prostate gland morphology	Gt(ROSA)26Sor<tm1(SPOP*F133V)Mrbn>/Gt(ROSA)26Sor<+>,Tg(Pbsn-cre)4Prb/0	involves: C57BL/6 * DBA/2	N	28292441
MGI:6275174	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Gt(ROSA)26Sor<tm1(SPOP*F133V)Mrbn>/Gt(ROSA)26Sor<+>,Pten<tm2.1Ppp>/Pten<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	28292441
MGI:6275174	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Gt(ROSA)26Sor<tm1(SPOP*F133V)Mrbn>/Gt(ROSA)26Sor<+>,Pten<tm2.1Ppp>/Pten<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	28292441
MGI:6275175	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Gt(ROSA)26Sor<tm1(SPOP*F133V)Mrbn>/Gt(ROSA)26Sor<+>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * C57BL/6 * DBA/2	N	28292441
MGI:6275549	F	MP:0004896	abnormal endometrium morphology	Gt(ROSA)26Sor<tm2(CAG-Nr5a1)Fjd>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27018534
MGI:6275549	F	MP:0011873	enlarged uterine horn	Gt(ROSA)26Sor<tm2(CAG-Nr5a1)Fjd>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27018534
MGI:6275549	F	MP:0009251	enlarged endometrial glands	Gt(ROSA)26Sor<tm2(CAG-Nr5a1)Fjd>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27018534
MGI:6275549	F	MP:0003845	abnormal decidualization	Gt(ROSA)26Sor<tm2(CAG-Nr5a1)Fjd>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27018534
MGI:6275549	F	MP:0001926	female infertility	Gt(ROSA)26Sor<tm2(CAG-Nr5a1)Fjd>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27018534
MGI:6275549	F	MP:0009082	uterus cyst	Gt(ROSA)26Sor<tm2(CAG-Nr5a1)Fjd>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27018534
MGI:6275549	F	MP:0009080	uterus inflammation	Gt(ROSA)26Sor<tm2(CAG-Nr5a1)Fjd>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27018534
MGI:6275549	F	MP:0013400	abnormal endometrial gland development	Gt(ROSA)26Sor<tm2(CAG-Nr5a1)Fjd>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27018534
MGI:6275549	F	MP:0009094	abnormal endometrial gland morphology	Gt(ROSA)26Sor<tm2(CAG-Nr5a1)Fjd>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27018534
MGI:6275549	F	MP:0001120	abnormal uterus morphology	Gt(ROSA)26Sor<tm2(CAG-Nr5a1)Fjd>/Gt(ROSA)26Sor<+>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27018534
MGI:6275834	M	MP:0001559	hyperglycemia	Pik3r1<tm1.1Geno>/Pik3r1<+>	involves: C57BL/6 * C57BL/6J	N	26974159
MGI:6276000	M	MP:0003058	increased insulin secretion	Abhd6<tm1a(EUCOMM)Hmgu>/Abhd6<tm1a(EUCOMM)Hmgu>	C57BL/6N-Abhd6<tm1a(EUCOMM)Hmgu>	N	26997277
MGI:6276000	F	MP:0003059	decreased insulin secretion	Abhd6<tm1a(EUCOMM)Hmgu>/Abhd6<tm1a(EUCOMM)Hmgu>	C57BL/6N-Abhd6<tm1a(EUCOMM)Hmgu>	N	26997277
MGI:6276000	F	MP:0001262	decreased body weight	Abhd6<tm1a(EUCOMM)Hmgu>/Abhd6<tm1a(EUCOMM)Hmgu>	C57BL/6N-Abhd6<tm1a(EUCOMM)Hmgu>	N	26997277
MGI:6276302	M	MP:0000745	tremors	Kctd1<Mhdahst014>/Kctd1<+>	C3HeB/FeJ-Kctd1<Mhdahst014>	N	28818080
MGI:6276302	F	MP:0000194	increased circulating calcium level	Kctd1<Mhdahst014>/Kctd1<+>	C3HeB/FeJ-Kctd1<Mhdahst014>	N	28818080
MGI:6276626	F	MP:0004762	increased anti-double stranded DNA antibody level	Fgl1<tm1b(EUCOMM)Hmgu>/Fgl1<tm1b(EUCOMM)Hmgu>	involves: BALB/cJ * C57BL/6N	N	30580966
MGI:6278109	F	MP:0005659	decreased susceptibility to diet-induced obesity	Chchd4<Gt(IST11943B12)Tigm>/Chchd4<+>	involves: C57BL/6N	N	26178476
MGI:6279204	F	MP:0005384	cellular phenotype	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	Y	26247513
MGI:6279204	M	MP:0001156	abnormal spermatogenesis	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	M	MP:0014052	increased male germ cell apoptosis	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	M	MP:0005584	abnormal enzyme/coenzyme activity	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	M	MP:0004762	increased anti-double stranded DNA antibody level	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	M	MP:0002118	abnormal lipid homeostasis	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	M	MP:0011603	decreased glutathione peroxidase activity	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	F	MP:0005376	homeostasis/metabolism phenotype	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	Y	26247513
MGI:6279204	M	MP:0005376	homeostasis/metabolism phenotype	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	Y	20692336
MGI:6279204	F	MP:0003507	abnormal ovary physiology	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	26247513
MGI:6279204	M	MP:0005371	limbs/digits/tail phenotype	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	Y	20692336
MGI:6279204	F	MP:0009433	polyovular ovarian follicle	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	26247513
MGI:6279204	M	MP:0002687	oligozoospermia	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	M	MP:0010768	mortality/aging	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	Y	20692336
MGI:6279204	M	MP:0005367	renal/urinary system phenotype	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	Y	20692336
MGI:6279204	M	MP:0012604	decreased glutathione level	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	F	MP:0008995	early reproductive senescence	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	26247513
MGI:6279204	M	MP:0004852	decreased testis weight	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	M	MP:0001154	seminiferous tubule degeneration	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	F	MP:0012604	decreased glutathione level	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	26247513
MGI:6279204	F	MP:0011129	decreased tertiary ovarian follicle number	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	26247513
MGI:6279204	F	MP:0011121	decreased primordial ovarian follicle number	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	26247513
MGI:6279204	M	MP:0005319	abnormal enzyme/coenzyme level	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	M	MP:0002675	asthenozoospermia	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	F	MP:0005319	abnormal enzyme/coenzyme level	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	26247513
MGI:6279204	M	MP:0005386	behavior/neurological phenotype	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	Y	20692336
MGI:6279204	M	MP:0006362	abnormal male germ cell morphology	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	M	MP:0004929	decreased epididymis weight	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	M	MP:0001922	reduced male fertility	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	M	MP:0002216	abnormal seminiferous tubule morphology	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279204	M	MP:0003674	oxidative stress	Nfe2l2<tm1Ywk>/Nfe2l2<tm1Ywk>	B6.129X1-Nfe2l2<tm1Ywk>	N	20692336
MGI:6279297	F	MP:0001259	abnormal body weight	Grn<tm1.1Aidi>/Grn<tm1.1Aidi>	involves: C57BL/6J	N	30271659
MGI:6280313	F	MP:0002016	ovary cyst	Spata22<repro42>/Spata22<repro42>	C3.B6-Spata22<repro42>	N	28297563
MGI:6280313	F	MP:0005431	decreased oocyte number	Spata22<repro42>/Spata22<repro42>	C3.B6-Spata22<repro42>	N	28297563
MGI:6280313	M	MP:0004901	decreased male germ cell number	Spata22<repro42>/Spata22<repro42>	C3.B6-Spata22<repro42>	N	28297563
MGI:6280314	F	MP:0002016	ovary cyst	Spata22<repro42>/Spata22<tm1a(KOMP)Wtsi>	involves: C3H * C57BL/6N	N	28297563
MGI:6280314	F	MP:0004805	absent oocytes	Spata22<repro42>/Spata22<tm1a(KOMP)Wtsi>	involves: C3H * C57BL/6N	N	28297563
MGI:6280314	M	MP:0004901	decreased male germ cell number	Spata22<repro42>/Spata22<tm1a(KOMP)Wtsi>	involves: C3H * C57BL/6N	N	28297563
MGI:6280314	M	MP:0005159	azoospermia	Spata22<repro42>/Spata22<tm1a(KOMP)Wtsi>	involves: C3H * C57BL/6N	N	28297563
MGI:6280314	M	MP:0008261	arrest of male meiosis	Spata22<repro42>/Spata22<tm1a(KOMP)Wtsi>	involves: C3H * C57BL/6N	N	28297563
MGI:6280314	M	MP:0001147	small testis	Spata22<repro42>/Spata22<tm1a(KOMP)Wtsi>	involves: C3H * C57BL/6N	N	28297563
MGI:6280314	F	MP:0001926	female infertility	Spata22<repro42>/Spata22<tm1a(KOMP)Wtsi>	involves: C3H * C57BL/6N	N	28297563
MGI:6280314	F	MP:0001131	abnormal ovarian follicle morphology	Spata22<repro42>/Spata22<tm1a(KOMP)Wtsi>	involves: C3H * C57BL/6N	N	28297563
MGI:6280314	M	MP:0001925	male infertility	Spata22<repro42>/Spata22<tm1a(KOMP)Wtsi>	involves: C3H * C57BL/6N	N	28297563
MGI:6280314	F	MP:0001127	small ovary	Spata22<repro42>/Spata22<tm1a(KOMP)Wtsi>	involves: C3H * C57BL/6N	N	28297563
MGI:6280316	M	MP:0001925	male infertility	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6280316	M	MP:0006380	abnormal spermatid morphology	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6280316	F	MP:0001926	female infertility	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6280316	F	MP:0004805	absent oocytes	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6280316	M	MP:0001147	small testis	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6280316	M	MP:0004901	decreased male germ cell number	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6280316	M	MP:0004852	decreased testis weight	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6280316	F	MP:0001127	small ovary	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6280316	M	MP:0005159	azoospermia	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6280316	F	MP:0005168	abnormal female meiosis	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6280316	M	MP:0006379	abnormal spermatocyte morphology	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6280316	M	MP:0001155	arrest of spermatogenesis	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6280316	M	MP:0008261	arrest of male meiosis	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6280316	F	MP:0001131	abnormal ovarian follicle morphology	Spata22<tm1a(KOMP)Wtsi>/Spata22<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	28297563
MGI:6281661	M	MP:0002674	abnormal sperm motility	Ccdc87<tm1(KOMP)Vlcg>/Ccdc87<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	29733332
MGI:6281661	M	MP:0005389	reproductive system phenotype	Ccdc87<tm1(KOMP)Vlcg>/Ccdc87<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	Y	29733332
MGI:6281661	M	MP:0001922	reduced male fertility	Ccdc87<tm1(KOMP)Vlcg>/Ccdc87<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	29733332
MGI:6281661	M	MP:0031354	abnormal acrosome assembly	Ccdc87<tm1(KOMP)Vlcg>/Ccdc87<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	29733332
MGI:6281661	M	MP:0001925	male infertility	Ccdc87<tm1(KOMP)Vlcg>/Ccdc87<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	29733332
MGI:6281661	M	MP:0009232	abnormal sperm nucleus morphology	Ccdc87<tm1(KOMP)Vlcg>/Ccdc87<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	29733332
MGI:6281661	M	MP:0004542	impaired acrosome reaction	Ccdc87<tm1(KOMP)Vlcg>/Ccdc87<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	29733332
MGI:6281661	M	MP:0009230	abnormal sperm head morphology	Ccdc87<tm1(KOMP)Vlcg>/Ccdc87<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	29733332
MGI:6281662	F	MP:0001926	female infertility	Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	30626716
MGI:6281662	F	MP:0020253	increased collagen level	Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	30626716
MGI:6281662	F	MP:0009662	abnormal uterine receptivity	Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	30626716
MGI:6281662	F	MP:0009666	abnormal embryo attachment	Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	30626716
MGI:6281662	F	MP:0009671	abnormal uterus physiology	Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	30626716
MGI:6281662	F	MP:0005389	reproductive system phenotype	Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	Y	30626716
MGI:6281662	F	MP:0001728	failure of embryo implantation	Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	30626716
MGI:6281662	F	MP:0004896	abnormal endometrium morphology	Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	30626716
MGI:6281662	F	MP:0003845	abnormal decidualization	Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	30626716
MGI:6281662	F	MP:0013399	endometrium fibrosis	Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	N	30626716
MGI:6281662	F	MP:0005376	homeostasis/metabolism phenotype	Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	Y	30626716
MGI:6283322	M	MP:0002169	no abnormal phenotype detected	Ercc6l<tm1.1Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283323	F	MP:0002169	no abnormal phenotype detected	Ercc6l<tm1.1Ajlc>/Ercc6l<+>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283324	F	MP:0002169	no abnormal phenotype detected	Ercc6l<tm1.1Ajlc>/Ercc6l<tm1.1Ajlc>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	Y	30232008
MGI:6283327	M	MP:0004045	abnormal cell cycle checkpoint function	Ercc6l<tm1.2Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283327	M	MP:0005621	abnormal cell physiology	Ercc6l<tm1.2Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283327	M	MP:0003111	abnormal cell nucleus morphology	Ercc6l<tm1.2Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283327	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Ercc6l<tm1.2Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283327	M	MP:0008057	abnormal DNA replication	Ercc6l<tm1.2Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283327	M	MP:0008008	early cellular replicative senescence	Ercc6l<tm1.2Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283327	M	MP:0004025	polyploidy	Ercc6l<tm1.2Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283327	M	MP:0014178	increased brain apoptosis	Ercc6l<tm1.2Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283327	M	MP:0013504	increased embryonic tissue cell apoptosis	Ercc6l<tm1.2Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283327	M	MP:0001730	embryonic growth arrest	Ercc6l<tm1.2Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283327	M	MP:0011704	decreased fibroblast proliferation	Ercc6l<tm1.2Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283327	M	MP:0008866	chromosomal instability	Ercc6l<tm1.2Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283327	M	MP:0001698	decreased embryo size	Ercc6l<tm1.2Ajlc>/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283337	F	MP:0005621	abnormal cell physiology	Ercc6l<tm1.2Ajlc>/Ercc6l<+>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283337	F	MP:0003111	abnormal cell nucleus morphology	Ercc6l<tm1.2Ajlc>/Ercc6l<+>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283337	F	MP:0008866	chromosomal instability	Ercc6l<tm1.2Ajlc>/Ercc6l<+>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283337	F	MP:0011704	decreased fibroblast proliferation	Ercc6l<tm1.2Ajlc>/Ercc6l<+>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283337	F	MP:0001935	decreased litter size	Ercc6l<tm1.2Ajlc>/Ercc6l<+>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283337	F	MP:0001926	female infertility	Ercc6l<tm1.2Ajlc>/Ercc6l<+>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283337	F	MP:0001923	reduced female fertility	Ercc6l<tm1.2Ajlc>/Ercc6l<+>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283337	F	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance	Ercc6l<tm1.2Ajlc>/Ercc6l<+>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283343	M	MP:0008866	chromosomal instability	Ercc6l<tm1.2Ajlc>/Y,Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283343	M	MP:0011092	embryonic lethality, complete penetrance	Ercc6l<tm1.2Ajlc>/Y,Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283343	M	MP:0001698	decreased embryo size	Ercc6l<tm1.2Ajlc>/Y,Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283343	M	MP:0013504	increased embryonic tissue cell apoptosis	Ercc6l<tm1.2Ajlc>/Y,Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283344	M	MP:0013504	increased embryonic tissue cell apoptosis	Ercc6l<tm1.2Ajlc>/Y,Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283344	M	MP:0011092	embryonic lethality, complete penetrance	Ercc6l<tm1.2Ajlc>/Y,Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283344	M	MP:0008866	chromosomal instability	Ercc6l<tm1.2Ajlc>/Y,Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283345	F	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance	Ercc6l<tm1.2Ajlc>/Ercc6l<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J	N	30232008
MGI:6283412	M	MP:0002635	reduced sensorimotor gating	Nrg3<tm1.1Plet>/Nrg3<tm1.1Plet>	involves: C57BL/6	N	27606322
MGI:6283412	M	MP:0009142	decreased prepulse inhibition	Nrg3<tm1.1Plet>/Nrg3<tm1.1Plet>	involves: C57BL/6	N	27606322
MGI:6283412	M	MP:0005386	behavior/neurological phenotype	Nrg3<tm1.1Plet>/Nrg3<tm1.1Plet>	involves: C57BL/6	Y	27606322
MGI:6283412	M	MP:0001415	increased exploration in new environment	Nrg3<tm1.1Plet>/Nrg3<tm1.1Plet>	involves: C57BL/6	N	27606322
MGI:6283412	M	MP:0003631	nervous system phenotype	Nrg3<tm1.1Plet>/Nrg3<tm1.1Plet>	involves: C57BL/6	Y	27606322
MGI:6283412	M	MP:0009456	impaired cued conditioning behavior	Nrg3<tm1.1Plet>/Nrg3<tm1.1Plet>	involves: C57BL/6	N	27606322
MGI:6283447	M	MP:0002687	oligozoospermia	Carm1<tm1.1Mtb>/Carm1<tm1.1Mtb>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	29659998
MGI:6283447	M	MP:0004901	decreased male germ cell number	Carm1<tm1.1Mtb>/Carm1<tm1.1Mtb>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	29659998
MGI:6283447	M	MP:0002675	asthenozoospermia	Carm1<tm1.1Mtb>/Carm1<tm1.1Mtb>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	29659998
MGI:6283447	M	MP:0001935	decreased litter size	Carm1<tm1.1Mtb>/Carm1<tm1.1Mtb>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	29659998
MGI:6283447	M	MP:0009234	absent sperm head	Carm1<tm1.1Mtb>/Carm1<tm1.1Mtb>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	29659998
MGI:6283447	M	MP:0001932	abnormal spermiogenesis	Carm1<tm1.1Mtb>/Carm1<tm1.1Mtb>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	29659998
MGI:6283447	M	MP:0006380	abnormal spermatid morphology	Carm1<tm1.1Mtb>/Carm1<tm1.1Mtb>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	29659998
MGI:6283447	M	MP:0002662	abnormal cauda epididymis morphology	Carm1<tm1.1Mtb>/Carm1<tm1.1Mtb>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	29659998
MGI:6283447	M	MP:0001922	reduced male fertility	Carm1<tm1.1Mtb>/Carm1<tm1.1Mtb>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	29659998
MGI:6283447	M	MP:0004852	decreased testis weight	Carm1<tm1.1Mtb>/Carm1<tm1.1Mtb>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	29659998
MGI:6283447	M	MP:0009230	abnormal sperm head morphology	Carm1<tm1.1Mtb>/Carm1<tm1.1Mtb>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	29659998
MGI:6283447	M	MP:0009831	abnormal sperm midpiece morphology	Carm1<tm1.1Mtb>/Carm1<tm1.1Mtb>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	29659998
MGI:6283447	M	MP:0001925	male infertility	Carm1<tm1.1Mtb>/Carm1<tm1.1Mtb>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	29659998
MGI:6283591	M	MP:0001154	seminiferous tubule degeneration	Nf1<Mhdadsk9>/Nf1<+>	involves: C3HeB/FeJ * C57BL/6	N	30571760
MGI:6283591	M	MP:0004182	abnormal spermiation	Nf1<Mhdadsk9>/Nf1<+>	involves: C3HeB/FeJ * C57BL/6	N	30571760
MGI:6283591	M	MP:0001156	abnormal spermatogenesis	Nf1<Mhdadsk9>/Nf1<+>	involves: C3HeB/FeJ * C57BL/6	N	30571760
MGI:6283591	M	MP:0009233	enlarged sperm head	Nf1<Mhdadsk9>/Nf1<+>	involves: C3HeB/FeJ * C57BL/6	N	30571760
MGI:6283591	M	MP:0020355	abnormal Sertoli cell barrier morphology	Nf1<Mhdadsk9>/Nf1<+>	involves: C3HeB/FeJ * C57BL/6	N	30571760
MGI:6283591	M	MP:0001935	decreased litter size	Nf1<Mhdadsk9>/Nf1<+>	involves: C3HeB/FeJ * C57BL/6	N	30571760
MGI:6283591	M	MP:0030603	increased sperm number	Nf1<Mhdadsk9>/Nf1<+>	involves: C3HeB/FeJ * C57BL/6	N	30571760
MGI:6283591	M	MP:0001148	enlarged testis	Nf1<Mhdadsk9>/Nf1<+>	involves: C3HeB/FeJ * C57BL/6	N	30571760
MGI:6283591	M	MP:0001922	reduced male fertility	Nf1<Mhdadsk9>/Nf1<+>	involves: C3HeB/FeJ * C57BL/6	N	30571760
MGI:6283591	M	MP:0006380	abnormal spermatid morphology	Nf1<Mhdadsk9>/Nf1<+>	involves: C3HeB/FeJ * C57BL/6	N	30571760
MGI:6283591	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Nf1<Mhdadsk9>/Nf1<+>	involves: C3HeB/FeJ * C57BL/6	N	30571760
MGI:6283591	M	MP:0005536	decreased Leydig cell number	Nf1<Mhdadsk9>/Nf1<+>	involves: C3HeB/FeJ * C57BL/6	N	30571760
MGI:6283675	F	MP:0001260	increased body weight	Trpc1<M2Btlr>/Trpc1<M2Btlr>	C57BL/6J-Trpc1<M2Btlr>	N	MGI:6283672
MGI:6283682	M	MP:0001154	seminiferous tubule degeneration	Zfp296<tm1Miya>/Zfp296<tm1Miya>	B6.129P2-Zfp296<tm1Miya>	N	28963472
MGI:6283682	F	MP:0004856	decreased ovary weight	Zfp296<tm1Miya>/Zfp296<tm1Miya>	B6.129P2-Zfp296<tm1Miya>	N	28963472
MGI:6283682	M	MP:0004852	decreased testis weight	Zfp296<tm1Miya>/Zfp296<tm1Miya>	B6.129P2-Zfp296<tm1Miya>	N	28963472
MGI:6283682	M	MP:0001925	male infertility	Zfp296<tm1Miya>/Zfp296<tm1Miya>	B6.129P2-Zfp296<tm1Miya>	N	28963472
MGI:6283682	M	MP:0001147	small testis	Zfp296<tm1Miya>/Zfp296<tm1Miya>	B6.129P2-Zfp296<tm1Miya>	N	28963472
MGI:6283682	M	MP:0001156	abnormal spermatogenesis	Zfp296<tm1Miya>/Zfp296<tm1Miya>	B6.129P2-Zfp296<tm1Miya>	N	28963472
MGI:6283682	F	MP:0005431	decreased oocyte number	Zfp296<tm1Miya>/Zfp296<tm1Miya>	B6.129P2-Zfp296<tm1Miya>	N	28963472
MGI:6283682	M	MP:0004901	decreased male germ cell number	Zfp296<tm1Miya>/Zfp296<tm1Miya>	B6.129P2-Zfp296<tm1Miya>	N	28963472
MGI:6283682	M	MP:0002687	oligozoospermia	Zfp296<tm1Miya>/Zfp296<tm1Miya>	B6.129P2-Zfp296<tm1Miya>	N	28963472
MGI:6283682	F	MP:0001127	small ovary	Zfp296<tm1Miya>/Zfp296<tm1Miya>	B6.129P2-Zfp296<tm1Miya>	N	28963472
MGI:6283682	F	MP:0001926	female infertility	Zfp296<tm1Miya>/Zfp296<tm1Miya>	B6.129P2-Zfp296<tm1Miya>	N	28963472
MGI:6283819	M	MP:0003222	increased cardiomyocyte apoptosis	Creg1<tm1Yal>/Creg1<+>	involves: 129 * C57BL/6	N	27840305
MGI:6283819	M	MP:0003037	increased myocardial infarct size	Creg1<tm1Yal>/Creg1<+>	involves: 129 * C57BL/6	N	27840305
MGI:6283819	M	MP:0003710	abnormal physiological neovascularization	Creg1<tm1Yal>/Creg1<+>	involves: 129 * C57BL/6	N	24896341
MGI:6283819	M	MP:0004485	increased response of heart to induced stress	Creg1<tm1Yal>/Creg1<+>	involves: 129 * C57BL/6	N	27840305
MGI:6283819	M	MP:0008260	abnormal autophagy	Creg1<tm1Yal>/Creg1<+>	involves: 129 * C57BL/6	N	27840305
MGI:6284005	M	MP:0001925	male infertility	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	M	MP:0005169	abnormal male meiosis	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	M	MP:0004901	decreased male germ cell number	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	M	MP:0001156	abnormal spermatogenesis	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	F	MP:0011125	decreased primary ovarian follicle number	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	M	MP:0006379	abnormal spermatocyte morphology	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	31000436
MGI:6284005	M	MP:0002216	abnormal seminiferous tubule morphology	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	M	MP:0001153	small seminiferous tubules	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	F	MP:0005168	abnormal female meiosis	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	F	MP:0011121	decreased primordial ovarian follicle number	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	F	MP:0001126	abnormal ovary morphology	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	M	MP:0004852	decreased testis weight	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	F	MP:0031381	decreased secondary ovarian follicle number	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	F	MP:0001931	abnormal oogenesis	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	F	MP:0001926	female infertility	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284005	M	MP:0001146	abnormal testis morphology	Rec114<tm1(KOMP)Wtsi>/Rec114<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284009	F	MP:0031381	decreased secondary ovarian follicle number	Rec114<tm1.2(KOMP)Wtsi>/Rec114<tm1.2(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284009	M	MP:0001156	abnormal spermatogenesis	Rec114<tm1.2(KOMP)Wtsi>/Rec114<tm1.2(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284009	F	MP:0001126	abnormal ovary morphology	Rec114<tm1.2(KOMP)Wtsi>/Rec114<tm1.2(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284009	F	MP:0011125	decreased primary ovarian follicle number	Rec114<tm1.2(KOMP)Wtsi>/Rec114<tm1.2(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284009	M	MP:0004852	decreased testis weight	Rec114<tm1.2(KOMP)Wtsi>/Rec114<tm1.2(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284009	F	MP:0011121	decreased primordial ovarian follicle number	Rec114<tm1.2(KOMP)Wtsi>/Rec114<tm1.2(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284009	F	MP:0001931	abnormal oogenesis	Rec114<tm1.2(KOMP)Wtsi>/Rec114<tm1.2(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284009	M	MP:0001146	abnormal testis morphology	Rec114<tm1.2(KOMP)Wtsi>/Rec114<tm1.2(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6284009	M	MP:0002216	abnormal seminiferous tubule morphology	Rec114<tm1.2(KOMP)Wtsi>/Rec114<tm1.2(KOMP)Wtsi>	involves: C57BL/6N	N	30569039
MGI:6285119	M	MP:0002644	decreased circulating triglyceride level	Abca8b<tm1a(EUCOMM)Wtsi>/Abca8b<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	28882873
MGI:6285119	M	MP:0005179	decreased circulating cholesterol level	Abca8b<tm1a(EUCOMM)Wtsi>/Abca8b<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	28882873
MGI:6285119	M	MP:0000183	decreased circulating LDL cholesterol level	Abca8b<tm1a(EUCOMM)Wtsi>/Abca8b<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	28882873
MGI:6285119	M	MP:0000186	decreased circulating HDL cholesterol level	Abca8b<tm1a(EUCOMM)Wtsi>/Abca8b<tm1a(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	28882873
MGI:6285736	M	MP:0020869	immotile sperm	Dnaaf11<tm1.1Hmd>/Dnaaf11<tm1.1Hmd>,Nanos3<tm2.1(cre)Ysa>/Nanos3<+>	involves: 129S6/SvEvTac * C57BL/6NCrlj * CBA/JNCrlj	N	27353389
MGI:6286096	M	MP:0014115	cognitive inflexibility	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0012318	slow extinction of fear memory	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0001360	abnormal social investigation	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0008535	enlarged lateral ventricles	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0003459	increased fear-related response	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0004950	abnormal brain vasculature morphology	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0010053	decreased grip strength	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0001363	increased anxiety-related response	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0001417	decreased exploration in new environment	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0009142	decreased prepulse inhibition	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0008284	abnormal hippocampus pyramidal cell layer	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0001405	impaired coordination	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0001891	hydrocephaly	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0001489	decreased startle reflex	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0008432	abnormal long-term spatial reference memory	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0009455	enhanced cued conditioning behavior	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0001973	increased thermal nociceptive threshold	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0001262	decreased body weight	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286096	M	MP:0001409	increased stereotypic behavior	Arid1b<em1Iha>/Arid1b<+>	C57BL/6J-Arid1b<em1Iha>	N	28867767
MGI:6286132	F	MP:0002400	abnormal multipotent stem cell morphology	Dnmt3a<tm1Trow>/Dnmt3a<+>,Tg(Mx1-cre)1Cgn/0	B6.Cg-Dnmt3a<tm1Trow> Tg(Mx1-cre)1Cgn	N	30692594
MGI:6286132	F	MP:0004809	increased hematopoietic stem cell number	Dnmt3a<tm1Trow>/Dnmt3a<+>,Tg(Mx1-cre)1Cgn/0	B6.Cg-Dnmt3a<tm1Trow> Tg(Mx1-cre)1Cgn	N	30692594
MGI:6286132	F	MP:0013660	abnormal bone marrow hematopoietic cell morphology	Dnmt3a<tm1Trow>/Dnmt3a<+>,Tg(Mx1-cre)1Cgn/0	B6.Cg-Dnmt3a<tm1Trow> Tg(Mx1-cre)1Cgn	N	30692594
MGI:6286132	F	MP:0013891	increased common myeloid progenitor cell number	Dnmt3a<tm1Trow>/Dnmt3a<+>,Tg(Mx1-cre)1Cgn/0	B6.Cg-Dnmt3a<tm1Trow> Tg(Mx1-cre)1Cgn	N	30692594
MGI:6286134	F	MP:0013660	abnormal bone marrow hematopoietic cell morphology	Gt(ROSA)26Sor<tm3(CAG-flpo/ERT2)Alj>/Gt(ROSA)26Sor<+>,Npm1<tm1Trow>/Npm1<+>	B6.Cg-Gt(ROSA)26Sor<tm3(CAG-flpo/ERT2)Alj> Npm1<tm1Trow>	N	30692594
MGI:6286134	F	MP:0009278	abnormal bone marrow cell physiology	Gt(ROSA)26Sor<tm3(CAG-flpo/ERT2)Alj>/Gt(ROSA)26Sor<+>,Npm1<tm1Trow>/Npm1<+>	B6.Cg-Gt(ROSA)26Sor<tm3(CAG-flpo/ERT2)Alj> Npm1<tm1Trow>	N	30692594
MGI:6286134	F	MP:0004810	decreased hematopoietic stem cell number	Gt(ROSA)26Sor<tm3(CAG-flpo/ERT2)Alj>/Gt(ROSA)26Sor<+>,Npm1<tm1Trow>/Npm1<+>	B6.Cg-Gt(ROSA)26Sor<tm3(CAG-flpo/ERT2)Alj> Npm1<tm1Trow>	N	30692594
MGI:6286134	F	MP:0013696	increased granulocyte monocyte progenitor cell number	Gt(ROSA)26Sor<tm3(CAG-flpo/ERT2)Alj>/Gt(ROSA)26Sor<+>,Npm1<tm1Trow>/Npm1<+>	B6.Cg-Gt(ROSA)26Sor<tm3(CAG-flpo/ERT2)Alj> Npm1<tm1Trow>	N	30692594
MGI:6286136	F	MP:0009278	abnormal bone marrow cell physiology	Dnmt3a<tm1Trow>/Dnmt3a<+>,Gt(ROSA)26Sor<tm3(CAG-flpo/ERT2)Alj>/Gt(ROSA)26Sor<+>,Npm1<tm1Trow>/Npm1<+>,Tg(Mx1-cre)1Cgn/0	B6.Cg-Gt(ROSA)26Sor<tm3(CAG-flpo/ERT2)Alj> Npm1<tm1Trow> Dnmt3a<tm1Trow> Tg(Mx1-cre)1Cgn	N	30692594
MGI:6286247	M	MP:0004852	decreased testis weight	Fbxo7<tm1a(EUCOMM)Wtsi>/Fbxo7<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30840666
MGI:6286247	M	MP:0002687	oligozoospermia	Fbxo7<tm1a(EUCOMM)Wtsi>/Fbxo7<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30840666
MGI:6286247	M	MP:0001156	abnormal spermatogenesis	Fbxo7<tm1a(EUCOMM)Wtsi>/Fbxo7<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30840666
MGI:6286247	M	MP:0005578	teratozoospermia	Fbxo7<tm1a(EUCOMM)Wtsi>/Fbxo7<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30840666
MGI:6286247	M	MP:0001925	male infertility	Fbxo7<tm1a(EUCOMM)Wtsi>/Fbxo7<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30840666
MGI:6286247	M	MP:0020869	immotile sperm	Fbxo7<tm1a(EUCOMM)Wtsi>/Fbxo7<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30840666
MGI:6286247	M	MP:0008279	arrest of spermiogenesis	Fbxo7<tm1a(EUCOMM)Wtsi>/Fbxo7<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30840666
MGI:6286248	M	MP:0004768	abnormal axonal transport	Tg(Prnp-MAPT*P301S)50Hiw/0	B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw	N	24406748
MGI:6286248	M	MP:0002066	abnormal motor capabilities/coordination/movement	Tg(Prnp-MAPT*P301S)50Hiw/0	B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw	N	24406748
MGI:6286248	M	MP:0004250	tau protein deposits	Tg(Prnp-MAPT*P301S)50Hiw/0	B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw	N	24406748
MGI:6286248	M	MP:0005621	abnormal cell physiology	Tg(Prnp-MAPT*P301S)50Hiw/0	B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw	N	24406748
MGI:6286248	M	MP:0014370	impaired spatial working memory	Tg(Prnp-MAPT*P301S)50Hiw/0	B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw	N	24406748
MGI:6286248	M	MP:0001513	limb grasping	Tg(Prnp-MAPT*P301S)50Hiw/0	B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw	N	24406748
MGI:6286248	M	MP:0001262	decreased body weight	Tg(Prnp-MAPT*P301S)50Hiw/0	B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw	N	24406748
MGI:6286248	M	MP:0003461	abnormal response to novel object	Tg(Prnp-MAPT*P301S)50Hiw/0	B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw	N	24406748
MGI:6286248	M	MP:0002083	premature death	Tg(Prnp-MAPT*P301S)50Hiw/0	B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw	N	24406748
MGI:6286689	F	MP:0006035	abnormal mitochondrial morphology	Tg(Prnp-Immt/SOD1*G93A)7Gmnf/Tg(Prnp-Immt/SOD1*G93A)7Gmnf	involves: C57BL/6 * CBA * SJL	N	22049426
MGI:6286689	F	MP:0001194	dermatitis	Tg(Prnp-Immt/SOD1*G93A)7Gmnf/Tg(Prnp-Immt/SOD1*G93A)7Gmnf	involves: C57BL/6 * CBA * SJL	N	22049426
MGI:6286689	M	MP:0009105	penis prolapse	Tg(Prnp-Immt/SOD1*G93A)7Gmnf/Tg(Prnp-Immt/SOD1*G93A)7Gmnf	involves: C57BL/6 * CBA * SJL	N	22049426
MGI:6286689	F	MP:0011636	disorganized mitochondrial cristae	Tg(Prnp-Immt/SOD1*G93A)7Gmnf/Tg(Prnp-Immt/SOD1*G93A)7Gmnf	involves: C57BL/6 * CBA * SJL	N	22049426
MGI:6286689	F	MP:0010053	decreased grip strength	Tg(Prnp-Immt/SOD1*G93A)7Gmnf/Tg(Prnp-Immt/SOD1*G93A)7Gmnf	involves: C57BL/6 * CBA * SJL	N	22049426
MGI:6287125	M	MP:0002557	abnormal social/conspecific interaction behavior	Tg(tetO-DISC1*)70Plet/0,Tg(Camk2a-tTA)1Mmay/0	involves: C57BL/6 * CBA * SJL	N	17848917
MGI:6287125	F	MP:0008414	abnormal spatial reference memory	Tg(tetO-DISC1*)70Plet/0,Tg(Camk2a-tTA)1Mmay/0	involves: C57BL/6 * CBA * SJL	N	17848917
MGI:6287125	M	MP:0031391	increased locomotor activity	Tg(tetO-DISC1*)70Plet/0,Tg(Camk2a-tTA)1Mmay/0	involves: C57BL/6 * CBA * SJL	N	17848917
MGI:6287125	M	MP:0001354	increased aggression towards male mice	Tg(tetO-DISC1*)70Plet/0,Tg(Camk2a-tTA)1Mmay/0	involves: C57BL/6 * CBA * SJL	N	17848917
MGI:6287632	M	MP:0001925	male infertility	Vps13a<tm1Asan>/Vps13a<tm1Asan>	129S6.129S(B6)-Vps13a<tm1Asan>	N	29928881
MGI:6287632	M	MP:0014465	abnormal sperm mitochondrial morphology	Vps13a<tm1Asan>/Vps13a<tm1Asan>	129S6.129S(B6)-Vps13a<tm1Asan>	N	29928881
MGI:6287632	M	MP:0005389	reproductive system phenotype	Vps13a<tm1Asan>/Vps13a<tm1Asan>	129S6.129S(B6)-Vps13a<tm1Asan>	Y	29928881
MGI:6287632	M	MP:0002675	asthenozoospermia	Vps13a<tm1Asan>/Vps13a<tm1Asan>	129S6.129S(B6)-Vps13a<tm1Asan>	N	29928881
MGI:6287687	F	MP:0001926	female infertility	Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287687	M	MP:0001925	male infertility	Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287687	M	MP:0008261	arrest of male meiosis	Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287687	F	MP:0004856	decreased ovary weight	Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287687	F	MP:0002777	absent ovarian follicles	Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287687	M	MP:0004852	decreased testis weight	Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287687	M	MP:0005159	azoospermia	Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287687	F	MP:0013507	increased ovary apoptosis	Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287687	M	MP:0014052	increased male germ cell apoptosis	Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287688	F	MP:0005431	decreased oocyte number	Chek2<tm1Mak>/Chek2<tm1Mak>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287688	F	MP:0001923	reduced female fertility	Chek2<tm1Mak>/Chek2<tm1Mak>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287688	F	MP:0005389	reproductive system phenotype	Chek2<tm1Mak>/Chek2<tm1Mak>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	Y	30305635
MGI:6287688	M	MP:0002216	abnormal seminiferous tubule morphology	Chek2<tm1Mak>/Chek2<tm1Mak>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287688	F	MP:0001729	impaired embryo implantation	Chek2<tm1Mak>/Chek2<tm1Mak>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287688	F	MP:0011121	decreased primordial ovarian follicle number	Chek2<tm1Mak>/Chek2<tm1Mak>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287688	F	MP:0001935	decreased litter size	Chek2<tm1Mak>/Chek2<tm1Mak>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287688	M	MP:0002687	oligozoospermia	Chek2<tm1Mak>/Chek2<tm1Mak>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287688	M	MP:0004852	decreased testis weight	Chek2<tm1Mak>/Chek2<tm1Mak>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287688	F	MP:0009451	abnormal chromosomal synapsis	Chek2<tm1Mak>/Chek2<tm1Mak>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287688	M	MP:0001925	male infertility	Chek2<tm1Mak>/Chek2<tm1Mak>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287689	M	MP:0001925	male infertility	Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287689	F	MP:0013507	increased ovary apoptosis	Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287689	F	MP:0004856	decreased ovary weight	Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287689	F	MP:0001926	female infertility	Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287689	M	MP:0004852	decreased testis weight	Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287689	F	MP:0002777	absent ovarian follicles	Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287690	M	MP:0004852	decreased testis weight	Chek2<tm1Mak>/Chek2<tm1Mak>,Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287690	F	MP:0005389	reproductive system phenotype	Chek2<tm1Mak>/Chek2<tm1Mak>,Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	Y	30305635
MGI:6287690	F	MP:0001923	reduced female fertility	Chek2<tm1Mak>/Chek2<tm1Mak>,Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287690	F	MP:0011121	decreased primordial ovarian follicle number	Chek2<tm1Mak>/Chek2<tm1Mak>,Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287690	M	MP:0002216	abnormal seminiferous tubule morphology	Chek2<tm1Mak>/Chek2<tm1Mak>,Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287690	F	MP:0001935	decreased litter size	Chek2<tm1Mak>/Chek2<tm1Mak>,Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287690	M	MP:0002687	oligozoospermia	Chek2<tm1Mak>/Chek2<tm1Mak>,Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287690	M	MP:0001925	male infertility	Chek2<tm1Mak>/Chek2<tm1Mak>,Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287691	F	MP:0001926	female infertility	Swsap1<em1Mjn>/Swsap1<em1Mjn>,Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287691	M	MP:0001925	male infertility	Swsap1<em1Mjn>/Swsap1<em1Mjn>,Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287691	F	MP:0004856	decreased ovary weight	Swsap1<em1Mjn>/Swsap1<em1Mjn>,Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287691	M	MP:0004852	decreased testis weight	Swsap1<em1Mjn>/Swsap1<em1Mjn>,Zswim7<em1Mjn>/Zswim7<em1Mjn>	involves: C57BL/6J * CBA/J	N	30305635
MGI:6287692	M	MP:0001147	small testis	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd	N	30305635
MGI:6287693	M	MP:0004852	decreased testis weight	Brca2<tm1Kamc>/Brca2<tm1Kamc>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287693	M	MP:0008261	arrest of male meiosis	Brca2<tm1Kamc>/Brca2<tm1Kamc>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287693	M	MP:0009451	abnormal chromosomal synapsis	Brca2<tm1Kamc>/Brca2<tm1Kamc>,Swsap1<em1Mjn>/Swsap1<em1Mjn>	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	30305635
MGI:6287773	F	MP:0003078	aphakia	Ftx<tm1.1Oka>/Ftx<tm1.1Oka>	C57BL/6N-Ftx<tm1.1Oka>	N	30237402
MGI:6287773	F	MP:0001322	abnormal iris morphology	Ftx<tm1.1Oka>/Ftx<tm1.1Oka>	C57BL/6N-Ftx<tm1.1Oka>	N	30237402
MGI:6287773	F	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Ftx<tm1.1Oka>/Ftx<tm1.1Oka>	C57BL/6N-Ftx<tm1.1Oka>	N	30237402
MGI:6287773	F	MP:0005193	abnormal anterior eye segment morphology	Ftx<tm1.1Oka>/Ftx<tm1.1Oka>	C57BL/6N-Ftx<tm1.1Oka>	N	30237402
MGI:6287773	F	MP:0001297	microphthalmia	Ftx<tm1.1Oka>/Ftx<tm1.1Oka>	C57BL/6N-Ftx<tm1.1Oka>	N	30237402
MGI:6287775	F	MP:0005391	vision/eye phenotype	Mirc23<tm1.1Shbk>/Mirc23<tm1.1Shbk>	B6N.129(Cg)-Mirc23<tm1.1Shbk>	Y	30237402
MGI:6287820	F	MP:0005168	abnormal female meiosis	Ccnb3<em1Sky>/Ccnb3<em1Sky>	involves: C57BL/6J * CBA/J	N	30723090
MGI:6287820	F	MP:0005389	reproductive system phenotype	Ccnb3<em1Sky>/Ccnb3<em1Sky>	involves: C57BL/6J * CBA/J	Y	30723090
MGI:6287821	M	MP:0005389	reproductive system phenotype	Ccnb3<em1Sky>/Y	involves: C57BL/6J * CBA/J	Y	30723090
MGI:6287830	F	MP:0001297	microphthalmia	Ftx<tm1.1Oka>/Ftx<+>	C57BL/6N-Ftx<tm1.1Oka>	N	30237402
MGI:6287831	M	MP:0005391	vision/eye phenotype	Ftx<tm1.1Oka>/Y	C57BL/6N-Ftx<tm1.1Oka>	Y	30237402
MGI:6287832	F	MP:0005391	vision/eye phenotype	Mirc23<tm1.1Shbk>/Y	B6N.129(Cg)-Mirc23<tm1.1Shbk>	Y	30237402
MGI:6287871	M	MP:0001447	abnormal nest building behavior	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0001409	increased stereotypic behavior	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0008428	abnormal spatial working memory	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0001441	increased grooming behavior	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0011270	decreased excitatory postsynaptic current amplitude	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0031391	increased locomotor activity	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0001260	increased body weight	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0002912	abnormal excitatory postsynaptic potential	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0009936	abnormal dendritic spine morphology	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0001354	increased aggression towards male mice	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0012307	impaired spatial learning	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0003461	abnormal response to novel object	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0020551	abnormal postsynaptic density morphology	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0001360	abnormal social investigation	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6287871	M	MP:0001898	abnormal long-term depression	Gprasp2<tm1.1Jpe>/Y	B6.129(FVB)-Gprasp2<tm1.1Jpe>	N	30926797
MGI:6288307	M	MP:0000194	increased circulating calcium level	1500009L16Rik<em1(IMPC)Mbp>/1500009L16Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1500009L16Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288307	M	MP:0000063	decreased bone mineral density	1500009L16Rik<em1(IMPC)Mbp>/1500009L16Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1500009L16Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288308	F	MP:0001258	decreased body length	4833420G17Rik<em1(IMPC)Mbp>/4833420G17Rik<em1(IMPC)Mbp>	C57BL/6NCrl-4833420G17Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288308	M	MP:0002092	abnormal eye morphology	4833420G17Rik<em1(IMPC)Mbp>/4833420G17Rik<em1(IMPC)Mbp>	C57BL/6NCrl-4833420G17Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288308	M	MP:0000274	enlarged heart	4833420G17Rik<em1(IMPC)Mbp>/4833420G17Rik<em1(IMPC)Mbp>	C57BL/6NCrl-4833420G17Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288308	F	MP:0005344	increased circulating bilirubin level	4833420G17Rik<em1(IMPC)Mbp>/4833420G17Rik<em1(IMPC)Mbp>	C57BL/6NCrl-4833420G17Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288308	M	MP:0000266	abnormal heart morphology	4833420G17Rik<em1(IMPC)Mbp>/4833420G17Rik<em1(IMPC)Mbp>	C57BL/6NCrl-4833420G17Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288310	F	MP:0011960	abnormal eye anterior chamber depth	Abhd15<tm1b(KOMP)Wtsi>/Abhd15<tm1b(KOMP)Wtsi>	C57BL/6N-Abhd15<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288310	F	MP:0001488	increased startle reflex	Abhd15<tm1b(KOMP)Wtsi>/Abhd15<tm1b(KOMP)Wtsi>	C57BL/6N-Abhd15<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288310	F	MP:0010052	increased grip strength	Abhd15<tm1b(KOMP)Wtsi>/Abhd15<tm1b(KOMP)Wtsi>	C57BL/6N-Abhd15<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288311	F	MP:0005599	increased cardiac muscle contractility	Abitram<tm1b(EUCOMM)Wtsi>/Abitram<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abitram<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288311	M	MP:0002792	abnormal retina vasculature morphology	Abitram<tm1b(EUCOMM)Wtsi>/Abitram<tm1b(EUCOMM)Wtsi>	C57BL/6N-Abitram<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288312	F	MP:0001304	cataract	Acox3<em1(IMPC)J>/Acox3<em1(IMPC)J>	C57BL/6NJ-Acox3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288312	F	MP:0005293	impaired glucose tolerance	Acox3<em1(IMPC)J>/Acox3<em1(IMPC)J>	C57BL/6NJ-Acox3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288312	F	MP:0005565	increased blood urea nitrogen level	Acox3<em1(IMPC)J>/Acox3<em1(IMPC)J>	C57BL/6NJ-Acox3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288313	F	MP:0001415	increased exploration in new environment	Actr5<tm2b(EUCOMM)Wtsi>/Actr5<+>	C57BL/6N-Actr5<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288316	M	MP:0011962	increased cornea thickness	Adgrf4<tm2b(EUCOMM)Wtsi>/Adgrf4<tm2b(EUCOMM)Wtsi>	C57BL/6N-Adgrf4<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288317	M	MP:0000266	abnormal heart morphology	Aebp1<tm1.1(KOMP)Wtsi>/Aebp1<+>	C57BL/6N-Aebp1<tm1.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288317	M	MP:0000274	enlarged heart	Aebp1<tm1.1(KOMP)Wtsi>/Aebp1<+>	C57BL/6N-Aebp1<tm1.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288321	M	MP:0003642	absent seminal vesicle	Aimp1<em1(IMPC)Tcp>/Aimp1<em1(IMPC)Tcp>	C57BL/6NCrl-Aimp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288321	M	MP:0001697	abnormal embryo size	Aimp1<em1(IMPC)Tcp>/Aimp1<em1(IMPC)Tcp>	C57BL/6NCrl-Aimp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288321	M	MP:0001925	male infertility	Aimp1<em1(IMPC)Tcp>/Aimp1<em1(IMPC)Tcp>	C57BL/6NCrl-Aimp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288321	F	MP:0009709	hydrometra	Aimp1<em1(IMPC)Tcp>/Aimp1<em1(IMPC)Tcp>	C57BL/6NCrl-Aimp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288322	M	MP:0000063	decreased bone mineral density	Akap7<tm2b(EUCOMM)Hmgu>/Akap7<tm2b(EUCOMM)Hmgu>	C57BL/6N-Akap7<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288323	M	MP:0002067	abnormal sensory capabilities/reflexes/nociception	Alg6<em1(IMPC)Tcp>/Alg6<+>	C57BL/6NCrl-Alg6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288323	M	MP:0000702	enlarged lymph nodes	Alg6<em1(IMPC)Tcp>/Alg6<+>	C57BL/6NCrl-Alg6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288323	M	MP:0011874	enlarged urinary bladder	Alg6<em1(IMPC)Tcp>/Alg6<+>	C57BL/6NCrl-Alg6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288323	M	MP:0001417	decreased exploration in new environment	Alg6<em1(IMPC)Tcp>/Alg6<+>	C57BL/6NCrl-Alg6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288323	F	MP:0002060	abnormal skin morphology	Alg6<em1(IMPC)Tcp>/Alg6<+>	C57BL/6NCrl-Alg6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288324	F	MP:0001102	small superior vagus ganglion	Ankfy1<tm1b(KOMP)Mbp>/Ankfy1<+>	C57BL/6N-Ankfy1<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288324	F	MP:0009709	hydrometra	Ankfy1<tm1b(KOMP)Mbp>/Ankfy1<+>	C57BL/6N-Ankfy1<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288324	M	MP:0000266	abnormal heart morphology	Ankfy1<tm1b(KOMP)Mbp>/Ankfy1<+>	C57BL/6N-Ankfy1<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288324	F	MP:0000220	increased monocyte cell number	Ankfy1<tm1b(KOMP)Mbp>/Ankfy1<+>	C57BL/6N-Ankfy1<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288324	M	MP:0000274	enlarged heart	Ankfy1<tm1b(KOMP)Mbp>/Ankfy1<+>	C57BL/6N-Ankfy1<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288326	F	MP:0001415	increased exploration in new environment	Ankle2<em1(IMPC)Bay>/Ankle2<+>	C57BL/6N-Ankle2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288326	M	MP:0002792	abnormal retina vasculature morphology	Ankle2<em1(IMPC)Bay>/Ankle2<+>	C57BL/6N-Ankle2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288328	F	MP:0002968	increased circulating alkaline phosphatase level	Ankrd28<em1(IMPC)J>/Ankrd28<em1(IMPC)J>	C57BL/6NJ-Ankrd28<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288328	F	MP:0001402	decreased locomotor activity	Ankrd28<em1(IMPC)J>/Ankrd28<em1(IMPC)J>	C57BL/6NJ-Ankrd28<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288328	F	MP:0003179	thrombocytopenia	Ankrd28<em1(IMPC)J>/Ankrd28<em1(IMPC)J>	C57BL/6NJ-Ankrd28<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288329	M	MP:0000062	increased bone mineral density	Anks1<tm1b(KOMP)Wtsi>/Anks1<tm1b(KOMP)Wtsi>	C57BL/6N-Anks1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288329	M	MP:0000280	thin ventricular wall	Anks1<tm1b(KOMP)Wtsi>/Anks1<tm1b(KOMP)Wtsi>	C57BL/6N-Anks1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288329	M	MP:0010123	increased bone mineral content	Anks1<tm1b(KOMP)Wtsi>/Anks1<tm1b(KOMP)Wtsi>	C57BL/6N-Anks1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288330	M	MP:0010123	increased bone mineral content	Ap1ar<tm2b(EUCOMM)Hmgu>/Ap1ar<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ap1ar<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288330	M	MP:0003960	increased lean body mass	Ap1ar<tm2b(EUCOMM)Hmgu>/Ap1ar<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ap1ar<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288330	M	MP:0002753	dilated heart left ventricle	Ap1ar<tm2b(EUCOMM)Hmgu>/Ap1ar<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ap1ar<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288330	M	MP:0002833	increased heart weight	Ap1ar<tm2b(EUCOMM)Hmgu>/Ap1ar<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ap1ar<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288330	M	MP:0001510	abnormal coat appearance	Ap1ar<tm2b(EUCOMM)Hmgu>/Ap1ar<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ap1ar<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288331	M	MP:0001510	abnormal coat appearance	Ap4e1<em1(IMPC)Bay>/Ap4e1<+>	C57BL/6N-Ap4e1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288332	M	MP:0001491	unresponsive to tactile stimuli	Ap4e1<em1(IMPC)Bay>/Ap4e1<em1(IMPC)Bay>	C57BL/6N-Ap4e1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288332	M	MP:0001510	abnormal coat appearance	Ap4e1<em1(IMPC)Bay>/Ap4e1<em1(IMPC)Bay>	C57BL/6N-Ap4e1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288333	M	MP:0010123	increased bone mineral content	Aph1a<tm1b(KOMP)Mbp>/Aph1a<+>	C57BL/6N-Aph1a<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6288333	M	MP:0001510	abnormal coat appearance	Aph1a<tm1b(KOMP)Mbp>/Aph1a<+>	C57BL/6N-Aph1a<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6288333	F	MP:0001399	hyperactivity	Aph1a<tm1b(KOMP)Mbp>/Aph1a<+>	C57BL/6N-Aph1a<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6288334	F	MP:0010579	increased heart left ventricle size	Apol10b<tm1b(KOMP)Wtsi>/Apol10b<tm1b(KOMP)Wtsi>	C57BL/6N-Apol10b<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288337	M	MP:0000274	enlarged heart	Arhgef12<tm1b(KOMP)Wtsi>/Arhgef12<+>	C57BL/6N-Arhgef12<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288337	M	MP:0000266	abnormal heart morphology	Arhgef12<tm1b(KOMP)Wtsi>/Arhgef12<+>	C57BL/6N-Arhgef12<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288337	F	MP:0001402	decreased locomotor activity	Arhgef12<tm1b(KOMP)Wtsi>/Arhgef12<+>	C57BL/6N-Arhgef12<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288337	M	MP:0000277	abnormal heart shape	Arhgef12<tm1b(KOMP)Wtsi>/Arhgef12<+>	C57BL/6N-Arhgef12<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288337	F	MP:0009141	increased prepulse inhibition	Arhgef12<tm1b(KOMP)Wtsi>/Arhgef12<+>	C57BL/6N-Arhgef12<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288338	M	MP:0001697	abnormal embryo size	Arhgef12<tm1b(KOMP)Wtsi>/Arhgef12<tm1b(KOMP)Wtsi>	C57BL/6N-Arhgef12<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288338	M	MP:0003984	embryonic growth retardation	Arhgef12<tm1b(KOMP)Wtsi>/Arhgef12<tm1b(KOMP)Wtsi>	C57BL/6N-Arhgef12<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288339	F	MP:0002953	thick ventricular wall	Arhgef17<em1(IMPC)Bay>/Arhgef17<em1(IMPC)Bay>	C57BL/6N-Arhgef17<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288339	F	MP:0011110	preweaning lethality, incomplete penetrance	Arhgef17<em1(IMPC)Bay>/Arhgef17<em1(IMPC)Bay>	C57BL/6N-Arhgef17<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288339	F	MP:0003068	enlarged kidney	Arhgef17<em1(IMPC)Bay>/Arhgef17<em1(IMPC)Bay>	C57BL/6N-Arhgef17<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288340	M	MP:0010025	decreased total body fat amount	Arid4b<tm1b(EUCOMM)Wtsi>/Arid4b<+>	C57BL/6N-Arid4b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288340	F	MP:0002797	increased thigmotaxis	Arid4b<tm1b(EUCOMM)Wtsi>/Arid4b<+>	C57BL/6N-Arid4b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288340	F	MP:0001399	hyperactivity	Arid4b<tm1b(EUCOMM)Wtsi>/Arid4b<+>	C57BL/6N-Arid4b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288340	M	MP:0003960	increased lean body mass	Arid4b<tm1b(EUCOMM)Wtsi>/Arid4b<+>	C57BL/6N-Arid4b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288340	M	MP:0001325	abnormal retina morphology	Arid4b<tm1b(EUCOMM)Wtsi>/Arid4b<+>	C57BL/6N-Arid4b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288340	F	MP:0004924	abnormal behavior	Arid4b<tm1b(EUCOMM)Wtsi>/Arid4b<+>	C57BL/6N-Arid4b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288341	M	MP:0010088	decreased circulating fructosamine level	Armc2<tm1b(EUCOMM)Hmgu>/Armc2<+>	C57BL/6N-Armc2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288341	M	MP:0005343	increased circulating aspartate transaminase level	Armc2<tm1b(EUCOMM)Hmgu>/Armc2<+>	C57BL/6N-Armc2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288341	M	MP:0002941	increased circulating alanine transaminase level	Armc2<tm1b(EUCOMM)Hmgu>/Armc2<+>	C57BL/6N-Armc2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288341	M	MP:0005419	decreased circulating serum albumin level	Armc2<tm1b(EUCOMM)Hmgu>/Armc2<+>	C57BL/6N-Armc2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288341	M	MP:0000219	increased neutrophil cell number	Armc2<tm1b(EUCOMM)Hmgu>/Armc2<+>	C57BL/6N-Armc2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288342	M	MP:0000062	increased bone mineral density	Arrdc2<tm1b(EUCOMM)Wtsi>/Arrdc2<+>	C57BL/6N-Arrdc2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288345	M	MP:0001289	persistence of hyaloid vascular system	Atf7<tm2b(EUCOMM)Hmgu>/Atf7<tm2b(EUCOMM)Hmgu>	C57BL/6N-Atf7<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288350	F	MP:0003733	abnormal retina inner nuclear layer morphology	Rimoc1<tm1b(EUCOMM)Wtsi>/Rimoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rimoc1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288350	M	MP:0010097	abnormal retina blood vessel morphology	Rimoc1<tm1b(EUCOMM)Wtsi>/Rimoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rimoc1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288350	F	MP:0001415	increased exploration in new environment	Rimoc1<tm1b(EUCOMM)Wtsi>/Rimoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rimoc1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288350	F	MP:0000062	increased bone mineral density	Rimoc1<tm1b(EUCOMM)Wtsi>/Rimoc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rimoc1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288351	M	MP:0010570	prolonged ST segment	Awat1<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Awat1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288352	F	MP:0002060	abnormal skin morphology	B2m<tm1b(EUCOMM)Wtsi>/B2m<+>	C57BL/6N-B2m<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288352	F	MP:0009709	hydrometra	B2m<tm1b(EUCOMM)Wtsi>/B2m<+>	C57BL/6N-B2m<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288352	F	MP:0001566	increased circulating phosphate level	B2m<tm1b(EUCOMM)Wtsi>/B2m<+>	C57BL/6N-B2m<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288352	F	MP:0001102	small superior vagus ganglion	B2m<tm1b(EUCOMM)Wtsi>/B2m<+>	C57BL/6N-B2m<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288353	F	MP:0011100	preweaning lethality, complete penetrance	B2m<tm1b(EUCOMM)Wtsi>/B2m<tm1b(EUCOMM)Wtsi>	C57BL/6N-B2m<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288354	M	MP:0001364	decreased anxiety-related response	Bmp4<tm1b(EUCOMM)Hmgu>/Bmp4<+>	C57BL/6N-Bmp4<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288354	F	MP:0011965	decreased total retina thickness	Bmp4<tm1b(EUCOMM)Hmgu>/Bmp4<+>	C57BL/6N-Bmp4<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288354	F	MP:0001322	abnormal iris morphology	Bmp4<tm1b(EUCOMM)Hmgu>/Bmp4<+>	C57BL/6N-Bmp4<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288354	M	MP:0005176	eyelids fail to open	Bmp4<tm1b(EUCOMM)Hmgu>/Bmp4<+>	C57BL/6N-Bmp4<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288354	F	MP:0003731	abnormal retina outer nuclear layer morphology	Bmp4<tm1b(EUCOMM)Hmgu>/Bmp4<+>	C57BL/6N-Bmp4<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288354	M	MP:0001399	hyperactivity	Bmp4<tm1b(EUCOMM)Hmgu>/Bmp4<+>	C57BL/6N-Bmp4<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288354	F	MP:0001325	abnormal retina morphology	Bmp4<tm1b(EUCOMM)Hmgu>/Bmp4<+>	C57BL/6N-Bmp4<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288354	M	MP:0003733	abnormal retina inner nuclear layer morphology	Bmp4<tm1b(EUCOMM)Hmgu>/Bmp4<+>	C57BL/6N-Bmp4<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288354	F	MP:0011960	abnormal eye anterior chamber depth	Bmp4<tm1b(EUCOMM)Hmgu>/Bmp4<+>	C57BL/6N-Bmp4<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288356	M	MP:0009142	decreased prepulse inhibition	Bptf<em1(IMPC)Bay>/Bptf<+>	C57BL/6N-Bptf<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288356	F	MP:0001258	decreased body length	Bptf<em1(IMPC)Bay>/Bptf<+>	C57BL/6N-Bptf<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288357	F	MP:0011100	preweaning lethality, complete penetrance	Bptf<em1(IMPC)Bay>/Bptf<em1(IMPC)Bay>	C57BL/6N-Bptf<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288358	M	MP:0003720	abnormal neural tube closure	Brap<em1(IMPC)Mbp>/Brap<em1(IMPC)Mbp>	C57BL/6NCrl-Brap<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288359	M	MP:0010052	increased grip strength	Brd4<tm1b(EUCOMM)Wtsi>/Brd4<+>	C57BL/6N-Brd4<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288359	F	MP:0011959	abnormal eye posterior chamber depth	Brd4<tm1b(EUCOMM)Wtsi>/Brd4<+>	C57BL/6N-Brd4<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288359	F	MP:0009142	decreased prepulse inhibition	Brd4<tm1b(EUCOMM)Wtsi>/Brd4<+>	C57BL/6N-Brd4<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288359	M	MP:0010097	abnormal retina blood vessel morphology	Brd4<tm1b(EUCOMM)Wtsi>/Brd4<+>	C57BL/6N-Brd4<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288359	F	MP:0003731	abnormal retina outer nuclear layer morphology	Brd4<tm1b(EUCOMM)Wtsi>/Brd4<+>	C57BL/6N-Brd4<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288360	M	MP:0005655	increased aggression	Brms1l<em1(IMPC)J>/Brms1l<+>	C57BL/6NJ-Brms1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288361	M	MP:0000691	enlarged spleen	Btnl4<em1(IMPC)Tcp>/Btnl4<em1(IMPC)Tcp>	C57BL/6NCrl-Btnl4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288361	M	MP:0003233	prolonged QT interval	Btnl4<em1(IMPC)Tcp>/Btnl4<em1(IMPC)Tcp>	C57BL/6NCrl-Btnl4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288361	M	MP:0002060	abnormal skin morphology	Btnl4<em1(IMPC)Tcp>/Btnl4<em1(IMPC)Tcp>	C57BL/6NCrl-Btnl4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288361	M	MP:0010506	prolonged RR interval	Btnl4<em1(IMPC)Tcp>/Btnl4<em1(IMPC)Tcp>	C57BL/6NCrl-Btnl4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288361	M	MP:0000702	enlarged lymph nodes	Btnl4<em1(IMPC)Tcp>/Btnl4<em1(IMPC)Tcp>	C57BL/6NCrl-Btnl4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288361	M	MP:0010570	prolonged ST segment	Btnl4<em1(IMPC)Tcp>/Btnl4<em1(IMPC)Tcp>	C57BL/6NCrl-Btnl4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288364	F	MP:0001556	increased circulating HDL cholesterol level	C4bp<tm1b(KOMP)Wtsi>/C4bp<tm1b(KOMP)Wtsi>	C57BL/6N-C4bp<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6288365	F	MP:0000266	abnormal heart morphology	Cacna1f<tm1.1(KOMP)Vlcg>/Cacna1f<tm1.1(KOMP)Vlcg>	C57BL/6N-Cacna1f<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288365	F	MP:0001333	absent optic nerve	Cacna1f<tm1.1(KOMP)Vlcg>/Cacna1f<tm1.1(KOMP)Vlcg>	C57BL/6N-Cacna1f<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288365	F	MP:0002079	increased circulating insulin level	Cacna1f<tm1.1(KOMP)Vlcg>/Cacna1f<tm1.1(KOMP)Vlcg>	C57BL/6N-Cacna1f<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288365	F	MP:0001399	hyperactivity	Cacna1f<tm1.1(KOMP)Vlcg>/Cacna1f<tm1.1(KOMP)Vlcg>	C57BL/6N-Cacna1f<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288365	F	MP:0002092	abnormal eye morphology	Cacna1f<tm1.1(KOMP)Vlcg>/Cacna1f<tm1.1(KOMP)Vlcg>	C57BL/6N-Cacna1f<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288365	F	MP:0000274	enlarged heart	Cacna1f<tm1.1(KOMP)Vlcg>/Cacna1f<tm1.1(KOMP)Vlcg>	C57BL/6N-Cacna1f<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288366	F	MP:0001325	abnormal retina morphology	Cacna2d4<em1(IMPC)J>/Cacna2d4<em1(IMPC)J>	C57BL/6NJ-Cacna2d4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288368	M	MP:0003928	increased heart rate variability	Calhm6<tm2b(EUCOMM)Wtsi>/Calhm6<tm2b(EUCOMM)Wtsi>	C57BL/6N-Calhm6<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288370	F	MP:0005293	impaired glucose tolerance	Car13<tm1b(KOMP)Wtsi>/Car13<tm1b(KOMP)Wtsi>	C57BL/6N-Car13<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288371	M	MP:0010097	abnormal retina blood vessel morphology	Car14<tm1b(EUCOMM)Hmgu>/Car14<tm1b(EUCOMM)Hmgu>	C57BL/6N-Car14<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288371	F	MP:0010379	decreased respiratory quotient	Car14<tm1b(EUCOMM)Hmgu>/Car14<tm1b(EUCOMM)Hmgu>	C57BL/6N-Car14<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288371	M	MP:0002792	abnormal retina vasculature morphology	Car14<tm1b(EUCOMM)Hmgu>/Car14<tm1b(EUCOMM)Hmgu>	C57BL/6N-Car14<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288372	F	MP:0000194	increased circulating calcium level	Casr<tm1b(KOMP)Mbp>/Casr<+>	C57BL/6N-Casr<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288372	F	MP:0001102	small superior vagus ganglion	Casr<tm1b(KOMP)Mbp>/Casr<+>	C57BL/6N-Casr<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288372	M	MP:0001566	increased circulating phosphate level	Casr<tm1b(KOMP)Mbp>/Casr<+>	C57BL/6N-Casr<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288372	M	MP:0001944	abnormal pancreas morphology	Casr<tm1b(KOMP)Mbp>/Casr<+>	C57BL/6N-Casr<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288372	F	MP:0004906	enlarged uterus	Casr<tm1b(KOMP)Mbp>/Casr<+>	C57BL/6N-Casr<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288372	F	MP:0009142	decreased prepulse inhibition	Casr<tm1b(KOMP)Mbp>/Casr<+>	C57BL/6N-Casr<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288377	M	MP:0002546	mydriasis	Ccdc191<em1(IMPC)J>/Ccdc191<em1(IMPC)J>	C57BL/6NJ-Ccdc191<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288377	M	MP:0001925	male infertility	Ccdc191<em1(IMPC)J>/Ccdc191<em1(IMPC)J>	C57BL/6NJ-Ccdc191<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288379	M	MP:0000221	decreased leukocyte cell number	Ccdc88b<em1(IMPC)Tcp>/Ccdc88b<em1(IMPC)Tcp>	C57BL/6NCrl-Ccdc88b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288379	M	MP:0000702	enlarged lymph nodes	Ccdc88b<em1(IMPC)Tcp>/Ccdc88b<em1(IMPC)Tcp>	C57BL/6NCrl-Ccdc88b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288379	M	MP:0005016	decreased lymphocyte cell number	Ccdc88b<em1(IMPC)Tcp>/Ccdc88b<em1(IMPC)Tcp>	C57BL/6NCrl-Ccdc88b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288379	F	MP:0013278	decreased fasting circulating glucose level	Ccdc88b<em1(IMPC)Tcp>/Ccdc88b<em1(IMPC)Tcp>	C57BL/6NCrl-Ccdc88b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288379	F	MP:0008528	polycystic kidney	Ccdc88b<em1(IMPC)Tcp>/Ccdc88b<em1(IMPC)Tcp>	C57BL/6NCrl-Ccdc88b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288380	M	MP:0011874	enlarged urinary bladder	Cckar<tm1b(EUCOMM)Hmgu>/Cckar<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cckar<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288380	M	MP:0005343	increased circulating aspartate transaminase level	Cckar<tm1b(EUCOMM)Hmgu>/Cckar<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cckar<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288382	F	MP:0001304	cataract	Cdh7<em1(IMPC)J>/Cdh7<em1(IMPC)J>	C57BL/6NJ-Cdh7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288383	M	MP:0001304	cataract	Cdk2ap2<em1(IMPC)J>/Cdk2ap2<em1(IMPC)J>	C57BL/6NJ-Cdk2ap2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288383	F	MP:0002574	increased vertical activity	Cdk2ap2<em1(IMPC)J>/Cdk2ap2<em1(IMPC)J>	C57BL/6NJ-Cdk2ap2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288384	F	MP:0011100	preweaning lethality, complete penetrance	Cenpt<em1(IMPC)Bay>/Cenpt<em1(IMPC)Bay>	C57BL/6N-Cenpt<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288385	F	MP:0003731	abnormal retina outer nuclear layer morphology	Cep19<tm1b(EUCOMM)Hmgu>/Cep19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cep19<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288385	M	MP:0001258	decreased body length	Cep19<tm1b(EUCOMM)Hmgu>/Cep19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cep19<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288385	M	MP:0009142	decreased prepulse inhibition	Cep19<tm1b(EUCOMM)Hmgu>/Cep19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cep19<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288385	F	MP:0001926	female infertility	Cep19<tm1b(EUCOMM)Hmgu>/Cep19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cep19<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288385	M	MP:0003961	decreased lean body mass	Cep19<tm1b(EUCOMM)Hmgu>/Cep19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cep19<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288385	M	MP:0001925	male infertility	Cep19<tm1b(EUCOMM)Hmgu>/Cep19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cep19<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288385	M	MP:0001510	abnormal coat appearance	Cep19<tm1b(EUCOMM)Hmgu>/Cep19<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cep19<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288387	M	MP:0000219	increased neutrophil cell number	Cers1<tm1b(EUCOMM)Hmgu>/Cers1<+>	C57BL/6N-Cers1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288389	M	MP:0003394	increased cardiac output	Ces1a<tm1b(KOMP)Wtsi>/Ces1a<tm1b(KOMP)Wtsi>	C57BL/6N-Ces1a<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288390	M	MP:0001304	cataract	Cfap206<em1(IMPC)Mbp>/Cfap206<+>	C57BL/6NCrl-Cfap206<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288391	M	MP:0000759	abnormal skeletal muscle morphology	Cfap57<em1(IMPC)Mbp>/Cfap57<em1(IMPC)Mbp>	C57BL/6NCrl-Cfap57<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288391	M	MP:0001925	male infertility	Cfap57<em1(IMPC)Mbp>/Cfap57<em1(IMPC)Mbp>	C57BL/6NCrl-Cfap57<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288391	M	MP:0000955	abnormal spinal cord morphology	Cfap57<em1(IMPC)Mbp>/Cfap57<em1(IMPC)Mbp>	C57BL/6NCrl-Cfap57<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288392	F	MP:0002092	abnormal eye morphology	Cgnl1<em1(IMPC)Mbp>/Cgnl1<em1(IMPC)Mbp>	C57BL/6NCrl-Cgnl1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288392	M	MP:0004931	enlarged epididymis	Cgnl1<em1(IMPC)Mbp>/Cgnl1<em1(IMPC)Mbp>	C57BL/6NCrl-Cgnl1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288392	M	MP:0002631	abnormal epididymis morphology	Cgnl1<em1(IMPC)Mbp>/Cgnl1<em1(IMPC)Mbp>	C57BL/6NCrl-Cgnl1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288394	M	MP:0000219	increased neutrophil cell number	Chrna5<em1(IMPC)H>/Chrna5<em1(IMPC)H>	C57BL/6N-Chrna5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288394	F	MP:0002606	increased basophil cell number	Chrna5<em1(IMPC)H>/Chrna5<em1(IMPC)H>	C57BL/6N-Chrna5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288394	M	MP:0011239	abnormal skin coloration	Chrna5<em1(IMPC)H>/Chrna5<em1(IMPC)H>	C57BL/6N-Chrna5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288394	M	MP:0002875	decreased erythrocyte cell number	Chrna5<em1(IMPC)H>/Chrna5<em1(IMPC)H>	C57BL/6N-Chrna5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288394	M	MP:0005016	decreased lymphocyte cell number	Chrna5<em1(IMPC)H>/Chrna5<em1(IMPC)H>	C57BL/6N-Chrna5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288395	F	MP:0001312	abnormal cornea morphology	Cidea<tm1b(EUCOMM)Hmgu>/Cidea<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cidea<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6288395	F	MP:0001314	cornea opacity	Cidea<tm1b(EUCOMM)Hmgu>/Cidea<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cidea<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6288395	M	MP:0002965	increased circulating serum albumin level	Cidea<tm1b(EUCOMM)Hmgu>/Cidea<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cidea<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6288395	F	MP:0002968	increased circulating alkaline phosphatase level	Cidea<tm1b(EUCOMM)Hmgu>/Cidea<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cidea<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6288395	M	MP:0001258	decreased body length	Cidea<tm1b(EUCOMM)Hmgu>/Cidea<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cidea<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6288397	F	MP:0010052	increased grip strength	Cldn12<tm1b(EUCOMM)Wtsi>/Cldn12<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cldn12<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288398	M	MP:0001489	decreased startle reflex	Clic5<tm1b(EUCOMM)Hmgu>/Clic5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Clic5<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288399	F	MP:0001486	abnormal startle reflex	Clrn2<em1(IMPC)J>/Clrn2<em1(IMPC)J>	C57BL/6NJ-Clrn2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288399	M	MP:0009142	decreased prepulse inhibition	Clrn2<em1(IMPC)J>/Clrn2<em1(IMPC)J>	C57BL/6NJ-Clrn2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288399	M	MP:0003961	decreased lean body mass	Clrn2<em1(IMPC)J>/Clrn2<em1(IMPC)J>	C57BL/6NJ-Clrn2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288399	M	MP:0000063	decreased bone mineral density	Clrn2<em1(IMPC)J>/Clrn2<em1(IMPC)J>	C57BL/6NJ-Clrn2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288399	M	MP:0010024	increased total body fat amount	Clrn2<em1(IMPC)J>/Clrn2<em1(IMPC)J>	C57BL/6NJ-Clrn2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288399	M	MP:0010124	decreased bone mineral content	Clrn2<em1(IMPC)J>/Clrn2<em1(IMPC)J>	C57BL/6NJ-Clrn2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288401	F	MP:0010052	increased grip strength	Cnot10<em1(IMPC)J>/Cnot10<+>	C57BL/6NJ-Cnot10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288403	F	MP:0010053	decreased grip strength	Copb2<em1(IMPC)Bay>/Copb2<+>	C57BL/6N-Copb2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288403	F	MP:0001402	decreased locomotor activity	Copb2<em1(IMPC)Bay>/Copb2<+>	C57BL/6N-Copb2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288403	M	MP:0010025	decreased total body fat amount	Copb2<em1(IMPC)Bay>/Copb2<+>	C57BL/6N-Copb2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288403	M	MP:0003960	increased lean body mass	Copb2<em1(IMPC)Bay>/Copb2<+>	C57BL/6N-Copb2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288405	M	MP:0010124	decreased bone mineral content	Cpsf7<em1(IMPC)J>/Cpsf7<em1(IMPC)J>	C57BL/6NJ-Cpsf7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288405	M	MP:0001304	cataract	Cpsf7<em1(IMPC)J>/Cpsf7<em1(IMPC)J>	C57BL/6NJ-Cpsf7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288407	M	MP:0010052	increased grip strength	Csnk1g1<em1(IMPC)J>/Csnk1g1<em1(IMPC)J>	C57BL/6NJ-Csnk1g1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288407	F	MP:0002590	increased mean corpuscular volume	Csnk1g1<em1(IMPC)J>/Csnk1g1<em1(IMPC)J>	C57BL/6NJ-Csnk1g1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288407	F	MP:0001415	increased exploration in new environment	Csnk1g1<em1(IMPC)J>/Csnk1g1<em1(IMPC)J>	C57BL/6NJ-Csnk1g1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288407	M	MP:0000218	increased leukocyte cell number	Csnk1g1<em1(IMPC)J>/Csnk1g1<em1(IMPC)J>	C57BL/6NJ-Csnk1g1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288408	M	MP:0010052	increased grip strength	Cstf3<tm2b(EUCOMM)Hmgu>/Cstf3<+>	C57BL/6N-Cstf3<tm2b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288409	F	MP:0000062	increased bone mineral density	Ctsh<tm1b(KOMP)Wtsi>/Ctsh<tm1b(KOMP)Wtsi>	C57BL/6N-Ctsh<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288410	M	MP:0010378	increased respiratory quotient	Cx3cl1<em3(IMPC)Ics>/Cx3cl1<em3(IMPC)Ics>	C57BL/6N-Cx3cl1<em3(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6288410	M	MP:0002757	decreased vertical activity	Cx3cl1<em3(IMPC)Ics>/Cx3cl1<em3(IMPC)Ics>	C57BL/6N-Cx3cl1<em3(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6288411	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Cyp19a1<tm1b(EUCOMM)Hmgu>/Cyp19a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp19a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288411	M	MP:0000221	decreased leukocyte cell number	Cyp19a1<tm1b(EUCOMM)Hmgu>/Cyp19a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp19a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288411	F	MP:0002966	decreased circulating alkaline phosphatase level	Cyp19a1<tm1b(EUCOMM)Hmgu>/Cyp19a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp19a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288411	M	MP:0005178	increased circulating cholesterol level	Cyp19a1<tm1b(EUCOMM)Hmgu>/Cyp19a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp19a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288411	M	MP:0013279	increased fasting circulating glucose level	Cyp19a1<tm1b(EUCOMM)Hmgu>/Cyp19a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp19a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288411	F	MP:0005505	thrombocytosis	Cyp19a1<tm1b(EUCOMM)Hmgu>/Cyp19a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp19a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288411	M	MP:0000219	increased neutrophil cell number	Cyp19a1<tm1b(EUCOMM)Hmgu>/Cyp19a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp19a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288411	F	MP:0001417	decreased exploration in new environment	Cyp19a1<tm1b(EUCOMM)Hmgu>/Cyp19a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp19a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288411	M	MP:0005016	decreased lymphocyte cell number	Cyp19a1<tm1b(EUCOMM)Hmgu>/Cyp19a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp19a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288411	M	MP:0000745	tremors	Cyp19a1<tm1b(EUCOMM)Hmgu>/Cyp19a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp19a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288411	M	MP:0002965	increased circulating serum albumin level	Cyp19a1<tm1b(EUCOMM)Hmgu>/Cyp19a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp19a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288411	M	MP:0001406	abnormal gait	Cyp19a1<tm1b(EUCOMM)Hmgu>/Cyp19a1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp19a1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288412	F	MP:0002968	increased circulating alkaline phosphatase level	Dap3<em1(IMPC)J>/Dap3<+>	C57BL/6NJ-Dap3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288415	F	MP:0001399	hyperactivity	Dbn1<em1(IMPC)Bay>/Dbn1<em1(IMPC)Bay>	C57BL/6N-Dbn1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288415	M	MP:0001510	abnormal coat appearance	Dbn1<em1(IMPC)Bay>/Dbn1<em1(IMPC)Bay>	C57BL/6N-Dbn1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288417	F	MP:0005568	increased circulating total protein level	Ddx6<em1(IMPC)Mbp>/Ddx6<+>	C57BL/6N-Ddx6<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288417	F	MP:0002590	increased mean corpuscular volume	Ddx6<em1(IMPC)Mbp>/Ddx6<+>	C57BL/6N-Ddx6<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288417	M	MP:0000598	abnormal liver morphology	Ddx6<em1(IMPC)Mbp>/Ddx6<+>	C57BL/6N-Ddx6<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288417	M	MP:0002060	abnormal skin morphology	Ddx6<em1(IMPC)Mbp>/Ddx6<+>	C57BL/6N-Ddx6<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288417	M	MP:0002135	abnormal kidney morphology	Ddx6<em1(IMPC)Mbp>/Ddx6<+>	C57BL/6N-Ddx6<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288417	F	MP:0005561	increased mean corpuscular hemoglobin	Ddx6<em1(IMPC)Mbp>/Ddx6<+>	C57BL/6N-Ddx6<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288419	M	MP:0010506	prolonged RR interval	Dgkb<em1(IMPC)J>/Dgkb<em1(IMPC)J>	C57BL/6NJ-Dgkb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288419	M	MP:0005333	decreased heart rate	Dgkb<em1(IMPC)J>/Dgkb<em1(IMPC)J>	C57BL/6NJ-Dgkb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288420	F	MP:0010123	increased bone mineral content	Dguok<em1(IMPC)J>/Dguok<em1(IMPC)J>	C57BL/6NJ-Dguok<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288420	F	MP:0003961	decreased lean body mass	Dguok<em1(IMPC)J>/Dguok<em1(IMPC)J>	C57BL/6NJ-Dguok<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288420	M	MP:0001392	abnormal locomotor behavior	Dguok<em1(IMPC)J>/Dguok<em1(IMPC)J>	C57BL/6NJ-Dguok<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288420	F	MP:0001926	female infertility	Dguok<em1(IMPC)J>/Dguok<em1(IMPC)J>	C57BL/6NJ-Dguok<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288420	F	MP:0000063	decreased bone mineral density	Dguok<em1(IMPC)J>/Dguok<em1(IMPC)J>	C57BL/6NJ-Dguok<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288420	F	MP:0010024	increased total body fat amount	Dguok<em1(IMPC)J>/Dguok<em1(IMPC)J>	C57BL/6NJ-Dguok<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288421	F	MP:0001417	decreased exploration in new environment	Dhx16<tm1b(EUCOMM)Wtsi>/Dhx16<+>	C57BL/6N-Dhx16<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288421	M	MP:0002953	thick ventricular wall	Dhx16<tm1b(EUCOMM)Wtsi>/Dhx16<+>	C57BL/6N-Dhx16<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288422	F	MP:0002188	small heart	Disp3<em1(IMPC)Mbp>/Disp3<em1(IMPC)Mbp>	C57BL/6N-Disp3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288422	M	MP:0001146	abnormal testis morphology	Disp3<em1(IMPC)Mbp>/Disp3<em1(IMPC)Mbp>	C57BL/6N-Disp3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288422	F	MP:0000266	abnormal heart morphology	Disp3<em1(IMPC)Mbp>/Disp3<em1(IMPC)Mbp>	C57BL/6N-Disp3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288422	F	MP:0004832	enlarged ovary	Disp3<em1(IMPC)Mbp>/Disp3<em1(IMPC)Mbp>	C57BL/6N-Disp3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288422	M	MP:0000538	abnormal urinary bladder morphology	Disp3<em1(IMPC)Mbp>/Disp3<em1(IMPC)Mbp>	C57BL/6N-Disp3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288422	F	MP:0002135	abnormal kidney morphology	Disp3<em1(IMPC)Mbp>/Disp3<em1(IMPC)Mbp>	C57BL/6N-Disp3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288422	F	MP:0001126	abnormal ovary morphology	Disp3<em1(IMPC)Mbp>/Disp3<em1(IMPC)Mbp>	C57BL/6N-Disp3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288422	F	MP:0001120	abnormal uterus morphology	Disp3<em1(IMPC)Mbp>/Disp3<em1(IMPC)Mbp>	C57BL/6N-Disp3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288422	M	MP:0001147	small testis	Disp3<em1(IMPC)Mbp>/Disp3<em1(IMPC)Mbp>	C57BL/6N-Disp3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288422	M	MP:0011874	enlarged urinary bladder	Disp3<em1(IMPC)Mbp>/Disp3<em1(IMPC)Mbp>	C57BL/6N-Disp3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288422	F	MP:0009709	hydrometra	Disp3<em1(IMPC)Mbp>/Disp3<em1(IMPC)Mbp>	C57BL/6N-Disp3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288424	M	MP:0002060	abnormal skin morphology	Dlgap1<em1(IMPC)Tcp>/Dlgap1<em1(IMPC)Tcp>	C57BL/6NCrl-Dlgap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288424	F	MP:0001297	microphthalmia	Dlgap1<em1(IMPC)Tcp>/Dlgap1<em1(IMPC)Tcp>	C57BL/6NCrl-Dlgap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288424	F	MP:0002092	abnormal eye morphology	Dlgap1<em1(IMPC)Tcp>/Dlgap1<em1(IMPC)Tcp>	C57BL/6NCrl-Dlgap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288424	M	MP:0002768	small adrenal glands	Dlgap1<em1(IMPC)Tcp>/Dlgap1<em1(IMPC)Tcp>	C57BL/6NCrl-Dlgap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288424	M	MP:0001417	decreased exploration in new environment	Dlgap1<em1(IMPC)Tcp>/Dlgap1<em1(IMPC)Tcp>	C57BL/6NCrl-Dlgap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288424	F	MP:0001399	hyperactivity	Dlgap1<em1(IMPC)Tcp>/Dlgap1<em1(IMPC)Tcp>	C57BL/6NCrl-Dlgap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288425	M	MP:0006243	impaired pupillary reflex	Dnaaf4<tm1b(EUCOMM)Hmgu>/Dnaaf4<+>	C57BL/6N-Dnaaf4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6288425	F	MP:0001512	trunk curl	Dnaaf4<tm1b(EUCOMM)Hmgu>/Dnaaf4<+>	C57BL/6N-Dnaaf4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6288426	M	MP:0001925	male infertility	Dnah10<em1(IMPC)Bay>/Dnah10<em1(IMPC)Bay>	C57BL/6N-Dnah10<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288427	M	MP:0000063	decreased bone mineral density	Dnase1l2<em1(IMPC)Bay>/Dnase1l2<em1(IMPC)Bay>	C57BL/6N-Dnase1l2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288428	F	MP:0003731	abnormal retina outer nuclear layer morphology	Dnd1<em1(IMPC)Bay>/Dnd1<em1(IMPC)Bay>	C57BL/6N-Dnd1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288428	F	MP:0010024	increased total body fat amount	Dnd1<em1(IMPC)Bay>/Dnd1<em1(IMPC)Bay>	C57BL/6N-Dnd1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288428	F	MP:0003961	decreased lean body mass	Dnd1<em1(IMPC)Bay>/Dnd1<em1(IMPC)Bay>	C57BL/6N-Dnd1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288428	F	MP:0001926	female infertility	Dnd1<em1(IMPC)Bay>/Dnd1<em1(IMPC)Bay>	C57BL/6N-Dnd1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288428	F	MP:0000063	decreased bone mineral density	Dnd1<em1(IMPC)Bay>/Dnd1<em1(IMPC)Bay>	C57BL/6N-Dnd1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288428	F	MP:0010053	decreased grip strength	Dnd1<em1(IMPC)Bay>/Dnd1<em1(IMPC)Bay>	C57BL/6N-Dnd1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288428	F	MP:0010124	decreased bone mineral content	Dnd1<em1(IMPC)Bay>/Dnd1<em1(IMPC)Bay>	C57BL/6N-Dnd1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288428	M	MP:0001925	male infertility	Dnd1<em1(IMPC)Bay>/Dnd1<em1(IMPC)Bay>	C57BL/6N-Dnd1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288429	F	MP:0001914	hemorrhage	Dnmt3b<em1(IMPC)Mbp>/Dnmt3b<em1(IMPC)Mbp>	C57BL/6N-Dnmt3b<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288429	F	MP:0003743	abnormal facial morphology	Dnmt3b<em1(IMPC)Mbp>/Dnmt3b<em1(IMPC)Mbp>	C57BL/6N-Dnmt3b<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288429	F	MP:0001297	microphthalmia	Dnmt3b<em1(IMPC)Mbp>/Dnmt3b<em1(IMPC)Mbp>	C57BL/6N-Dnmt3b<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288430	M	MP:0001510	abnormal coat appearance	Dsg2<tm1b(EUCOMM)Wtsi>/Dsg2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dsg2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288430	M	MP:0011110	preweaning lethality, incomplete penetrance	Dsg2<tm1b(EUCOMM)Wtsi>/Dsg2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dsg2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288431	M	MP:0000266	abnormal heart morphology	Dstn<tm1b(KOMP)Wtsi>/Dstn<+>	C57BL/6N-Dstn<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6288431	M	MP:0000274	enlarged heart	Dstn<tm1b(KOMP)Wtsi>/Dstn<+>	C57BL/6N-Dstn<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6288433	F	MP:0005562	decreased mean corpuscular hemoglobin	Dtx3<em1(IMPC)J>/Dtx3<em1(IMPC)J>	C57BL/6NJ-Dtx3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288434	F	MP:0000639	abnormal adrenal gland morphology	Dusp12<em1(IMPC)Mbp>/Dusp12<+>	C57BL/6N-Dusp12<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288436	M	MP:0001146	abnormal testis morphology	Edc3<em1(IMPC)Tcp>/Edc3<+>	C57BL/6NCrl-Edc3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288436	M	MP:0002968	increased circulating alkaline phosphatase level	Edc3<em1(IMPC)Tcp>/Edc3<+>	C57BL/6NCrl-Edc3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288436	M	MP:0003068	enlarged kidney	Edc3<em1(IMPC)Tcp>/Edc3<+>	C57BL/6NCrl-Edc3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288436	M	MP:0002092	abnormal eye morphology	Edc3<em1(IMPC)Tcp>/Edc3<+>	C57BL/6NCrl-Edc3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288436	F	MP:0002135	abnormal kidney morphology	Edc3<em1(IMPC)Tcp>/Edc3<+>	C57BL/6NCrl-Edc3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288436	F	MP:0011874	enlarged urinary bladder	Edc3<em1(IMPC)Tcp>/Edc3<+>	C57BL/6NCrl-Edc3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288437	F	MP:0002941	increased circulating alanine transaminase level	Eea1<tm1b(EUCOMM)Hmgu>/Eea1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Eea1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288437	F	MP:0005343	increased circulating aspartate transaminase level	Eea1<tm1b(EUCOMM)Hmgu>/Eea1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Eea1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288439	F	MP:0009142	decreased prepulse inhibition	Efr3b<em1(IMPC)Mbp>/Efr3b<em1(IMPC)Mbp>	C57BL/6N-Efr3b<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288439	M	MP:0005554	decreased circulating creatinine level	Efr3b<em1(IMPC)Mbp>/Efr3b<em1(IMPC)Mbp>	C57BL/6N-Efr3b<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288439	F	MP:0001926	female infertility	Efr3b<em1(IMPC)Mbp>/Efr3b<em1(IMPC)Mbp>	C57BL/6N-Efr3b<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288439	M	MP:0005560	decreased circulating glucose level	Efr3b<em1(IMPC)Mbp>/Efr3b<em1(IMPC)Mbp>	C57BL/6N-Efr3b<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288440	F	MP:0004122	abnormal sinus arrhythmia	Egln3<tm1b(EUCOMM)Wtsi>/Egln3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Egln3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288440	M	MP:0008259	abnormal optic disk morphology	Egln3<tm1b(EUCOMM)Wtsi>/Egln3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Egln3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288441	M	MP:0001289	persistence of hyaloid vascular system	Eif2s2<em3(IMPC)Bay>/Eif2s2<+>	C57BL/6N-Eif2s2<em3(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288441	F	MP:0000689	abnormal spleen morphology	Eif2s2<em3(IMPC)Bay>/Eif2s2<+>	C57BL/6N-Eif2s2<em3(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288441	F	MP:0001399	hyperactivity	Eif2s2<em3(IMPC)Bay>/Eif2s2<+>	C57BL/6N-Eif2s2<em3(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288443	F	MP:0000280	thin ventricular wall	Eif4h<tm1b(EUCOMM)Wtsi>/Eif4h<+>	C57BL/6N-Eif4h<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288443	F	MP:0003733	abnormal retina inner nuclear layer morphology	Eif4h<tm1b(EUCOMM)Wtsi>/Eif4h<+>	C57BL/6N-Eif4h<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288444	F	MP:0010053	decreased grip strength	Emilin2<em1(IMPC)J>/Emilin2<em1(IMPC)J>	C57BL/6NJ-Emilin2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288444	M	MP:0001529	abnormal vocalization	Emilin2<em1(IMPC)J>/Emilin2<em1(IMPC)J>	C57BL/6NJ-Emilin2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288445	M	MP:0001925	male infertility	Enkur<em1(IMPC)Mbp>/Enkur<em1(IMPC)Mbp>	C57BL/6N-Enkur<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288445	M	MP:0001914	hemorrhage	Enkur<em1(IMPC)Mbp>/Enkur<em1(IMPC)Mbp>	C57BL/6N-Enkur<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288446	M	MP:0010025	decreased total body fat amount	Eps15l1<em1(IMPC)J>/Eps15l1<em1(IMPC)J>	C57BL/6NJ-Eps15l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288446	M	MP:0002590	increased mean corpuscular volume	Eps15l1<em1(IMPC)J>/Eps15l1<em1(IMPC)J>	C57BL/6NJ-Eps15l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288446	M	MP:0001319	irregularly shaped pupil	Eps15l1<em1(IMPC)J>/Eps15l1<em1(IMPC)J>	C57BL/6NJ-Eps15l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288448	F	MP:0000689	abnormal spleen morphology	Erg<em1(IMPC)Bay>/Erg<+>	C57BL/6N-Erg<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288448	M	MP:0001510	abnormal coat appearance	Erg<em1(IMPC)Bay>/Erg<+>	C57BL/6N-Erg<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288448	M	MP:0010579	increased heart left ventricle size	Erg<em1(IMPC)Bay>/Erg<+>	C57BL/6N-Erg<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288448	M	MP:0000221	decreased leukocyte cell number	Erg<em1(IMPC)Bay>/Erg<+>	C57BL/6N-Erg<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288450	M	MP:0005505	thrombocytosis	Ermn<em1(IMPC)H>/Ermn<em1(IMPC)H>	C57BL/6N-Ermn<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288450	M	MP:0005565	increased blood urea nitrogen level	Ermn<em1(IMPC)H>/Ermn<em1(IMPC)H>	C57BL/6N-Ermn<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288451	F	MP:0002874	decreased hemoglobin content	Esd<em1(IMPC)J>/Esd<em1(IMPC)J>	C57BL/6NJ-Esd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288451	F	MP:0000208	decreased hematocrit	Esd<em1(IMPC)J>/Esd<em1(IMPC)J>	C57BL/6NJ-Esd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288451	M	MP:0001488	increased startle reflex	Esd<em1(IMPC)J>/Esd<em1(IMPC)J>	C57BL/6NJ-Esd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288452	M	MP:0000274	enlarged heart	Esrp2<em1(IMPC)Tcp>/Esrp2<em1(IMPC)Tcp>	C57BL/6NCrl-Esrp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288452	M	MP:0000702	enlarged lymph nodes	Esrp2<em1(IMPC)Tcp>/Esrp2<em1(IMPC)Tcp>	C57BL/6NCrl-Esrp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288455	M	MP:0005561	increased mean corpuscular hemoglobin	Fabp7<em1(IMPC)H>/Fabp7<em1(IMPC)H>	C57BL/6N-Fabp7<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288455	M	MP:0002875	decreased erythrocyte cell number	Fabp7<em1(IMPC)H>/Fabp7<em1(IMPC)H>	C57BL/6N-Fabp7<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288456	F	MP:0001726	abnormal allantois morphology	Faf2<em1(IMPC)Mbp>/Faf2<em1(IMPC)Mbp>	C57BL/6N-Faf2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288456	M	MP:0003229	abnormal vitelline vasculature morphology	Faf2<em1(IMPC)Mbp>/Faf2<em1(IMPC)Mbp>	C57BL/6N-Faf2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288457	F	MP:0001402	decreased locomotor activity	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288457	M	MP:0001944	abnormal pancreas morphology	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288457	F	MP:0002966	decreased circulating alkaline phosphatase level	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288457	M	MP:0002059	abnormal seminal vesicle morphology	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288457	M	MP:0000219	increased neutrophil cell number	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288457	M	MP:0000274	enlarged heart	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288457	F	MP:0000470	abnormal stomach morphology	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288457	F	MP:0002100	abnormal tooth morphology	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288457	M	MP:0011874	enlarged urinary bladder	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288457	M	MP:0013278	decreased fasting circulating glucose level	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288457	F	MP:0001126	abnormal ovary morphology	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288457	M	MP:0005016	decreased lymphocyte cell number	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288457	M	MP:0002092	abnormal eye morphology	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288457	M	MP:0000157	abnormal sternum morphology	Fhip1b<em1(IMPC)Tcp>/Fhip1b<em1(IMPC)Tcp>	C57BL/6NCrl-Fhip1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288458	F	MP:0000689	abnormal spleen morphology	Fam209<tm1b(KOMP)Wtsi>/Fam209<tm1b(KOMP)Wtsi>	C57BL/6N-Fam209<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288460	M	MP:0001510	abnormal coat appearance	Fastkd2<tm1b(EUCOMM)Wtsi>/Fastkd2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fastkd2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288460	M	MP:0004953	decreased spleen weight	Fastkd2<tm1b(EUCOMM)Wtsi>/Fastkd2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fastkd2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288460	F	MP:0011110	preweaning lethality, incomplete penetrance	Fastkd2<tm1b(EUCOMM)Wtsi>/Fastkd2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fastkd2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288461	M	MP:0003450	enlarged pancreas	Fblim1<em5(IMPC)Tcp>/Fblim1<em5(IMPC)Tcp>	C57BL/6NCrl-Fblim1<em5(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288461	F	MP:0002764	short tibia	Fblim1<em5(IMPC)Tcp>/Fblim1<em5(IMPC)Tcp>	C57BL/6NCrl-Fblim1<em5(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288463	F	MP:0001312	abnormal cornea morphology	Fbxo21<em1(IMPC)J>/Fbxo21<em1(IMPC)J>	C57BL/6NJ-Fbxo21<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288465	F	MP:0000709	enlarged thymus	Fgd1<em1(IMPC)Tcp>/Fgd1<+>	C57BL/6NCrl-Fgd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288465	F	MP:0000428	abnormal craniofacial morphology	Fgd1<em1(IMPC)Tcp>/Fgd1<+>	C57BL/6NCrl-Fgd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288466	M	MP:0003425	abnormal optic vesicle formation	Fhod3<em1(IMPC)Mbp>/Fhod3<em1(IMPC)Mbp>	C57BL/6N-Fhod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288467	M	MP:0002833	increased heart weight	Fndc3b<tm1.1(KOMP)Vlcg>/Fndc3b<+>	C57BL/6N-Fndc3b<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6288467	M	MP:0009552	urinary bladder obstruction	Fndc3b<tm1.1(KOMP)Vlcg>/Fndc3b<+>	C57BL/6N-Fndc3b<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6288467	M	MP:0002092	abnormal eye morphology	Fndc3b<tm1.1(KOMP)Vlcg>/Fndc3b<+>	C57BL/6N-Fndc3b<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6288467	F	MP:0002075	abnormal coat/hair pigmentation	Fndc3b<tm1.1(KOMP)Vlcg>/Fndc3b<+>	C57BL/6N-Fndc3b<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6288468	M	MP:0010024	increased total body fat amount	Fos<em1(IMPC)Mbp>/Fos<+>	C57BL/6N-Fos<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288468	M	MP:0003961	decreased lean body mass	Fos<em1(IMPC)Mbp>/Fos<+>	C57BL/6N-Fos<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288469	M	MP:0001404	no spontaneous movement	Fos<em1(IMPC)Mbp>/Fos<em1(IMPC)Mbp>	C57BL/6N-Fos<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288473	F	MP:0011960	abnormal eye anterior chamber depth	Fzd8<em1(IMPC)Bay>/Fzd8<em1(IMPC)Bay>	C57BL/6N-Fzd8<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288473	M	MP:0005599	increased cardiac muscle contractility	Fzd8<em1(IMPC)Bay>/Fzd8<em1(IMPC)Bay>	C57BL/6N-Fzd8<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288473	M	MP:0002953	thick ventricular wall	Fzd8<em1(IMPC)Bay>/Fzd8<em1(IMPC)Bay>	C57BL/6N-Fzd8<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288474	F	MP:0011110	preweaning lethality, incomplete penetrance	Gcdh<tm2b(EUCOMM)Hmgu>/Gcdh<tm2b(EUCOMM)Hmgu>	C57BL/6N-Gcdh<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288474	F	MP:0010579	increased heart left ventricle size	Gcdh<tm2b(EUCOMM)Hmgu>/Gcdh<tm2b(EUCOMM)Hmgu>	C57BL/6N-Gcdh<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288475	M	MP:0009142	decreased prepulse inhibition	Gdpd5<tm1b(EUCOMM)Hmgu>/Gdpd5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gdpd5<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288475	F	MP:0011110	preweaning lethality, incomplete penetrance	Gdpd5<tm1b(EUCOMM)Hmgu>/Gdpd5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gdpd5<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288477	M	MP:0001312	abnormal cornea morphology	Gimap3<em1(IMPC)J>/Gimap3<em1(IMPC)J>	C57BL/6NJ-Gimap3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288478	F	MP:0001325	abnormal retina morphology	Gins4<tm1b(EUCOMM)Hmgu>/Gins4<+>	C57BL/6N-Gins4<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288478	F	MP:0001297	microphthalmia	Gins4<tm1b(EUCOMM)Hmgu>/Gins4<+>	C57BL/6N-Gins4<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288478	M	MP:0001488	increased startle reflex	Gins4<tm1b(EUCOMM)Hmgu>/Gins4<+>	C57BL/6N-Gins4<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288479	F	MP:0010097	abnormal retina blood vessel morphology	Gjc3<em1(IMPC)Bay>/Gjc3<em1(IMPC)Bay>	C57BL/6N-Gjc3<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288480	M	MP:0001556	increased circulating HDL cholesterol level	S2bpcox16<em1(IMPC)J>/S2bpcox16<em1(IMPC)J>	C57BL/6NJ-S2bpcox16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288480	F	MP:0002110	abnormal digit morphology	S2bpcox16<em1(IMPC)J>/S2bpcox16<em1(IMPC)J>	C57BL/6NJ-S2bpcox16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288480	M	MP:0005178	increased circulating cholesterol level	S2bpcox16<em1(IMPC)J>/S2bpcox16<em1(IMPC)J>	C57BL/6NJ-S2bpcox16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288480	M	MP:0005566	decreased blood urea nitrogen level	S2bpcox16<em1(IMPC)J>/S2bpcox16<em1(IMPC)J>	C57BL/6NJ-S2bpcox16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288484	F	MP:0000550	abnormal forelimb morphology	Golph3<em1(IMPC)Tcp>/Golph3<em1(IMPC)Tcp>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288484	F	MP:0000438	abnormal cranium morphology	Golph3<em1(IMPC)Tcp>/Golph3<em1(IMPC)Tcp>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288484	F	MP:0000689	abnormal spleen morphology	Golph3<em1(IMPC)Tcp>/Golph3<em1(IMPC)Tcp>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288484	M	MP:0001157	small seminal vesicle	Golph3<em1(IMPC)Tcp>/Golph3<em1(IMPC)Tcp>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288484	M	MP:0010124	decreased bone mineral content	Golph3<em1(IMPC)Tcp>/Golph3<em1(IMPC)Tcp>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288484	M	MP:0010052	increased grip strength	Golph3<em1(IMPC)Tcp>/Golph3<em1(IMPC)Tcp>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288484	M	MP:0002968	increased circulating alkaline phosphatase level	Golph3<em1(IMPC)Tcp>/Golph3<em1(IMPC)Tcp>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288484	M	MP:0002764	short tibia	Golph3<em1(IMPC)Tcp>/Golph3<em1(IMPC)Tcp>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288484	F	MP:0002060	abnormal skin morphology	Golph3<em1(IMPC)Tcp>/Golph3<em1(IMPC)Tcp>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288484	M	MP:0003795	abnormal bone structure	Golph3<em1(IMPC)Tcp>/Golph3<em1(IMPC)Tcp>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288484	F	MP:0011110	preweaning lethality, incomplete penetrance	Golph3<em1(IMPC)Tcp>/Golph3<em1(IMPC)Tcp>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288484	F	MP:0000709	enlarged thymus	Golph3<em1(IMPC)Tcp>/Golph3<em1(IMPC)Tcp>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288484	M	MP:0002599	increased mean platelet volume	Golph3<em1(IMPC)Tcp>/Golph3<em1(IMPC)Tcp>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288485	F	MP:0000702	enlarged lymph nodes	Golt1b<tm1b(EUCOMM)Wtsi>/Golt1b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Golt1b<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288485	M	MP:0010052	increased grip strength	Golt1b<tm1b(EUCOMM)Wtsi>/Golt1b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Golt1b<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288485	M	MP:0000709	enlarged thymus	Golt1b<tm1b(EUCOMM)Wtsi>/Golt1b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Golt1b<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288485	M	MP:0011874	enlarged urinary bladder	Golt1b<tm1b(EUCOMM)Wtsi>/Golt1b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Golt1b<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288485	M	MP:0003393	decreased cardiac output	Golt1b<tm1b(EUCOMM)Wtsi>/Golt1b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Golt1b<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288485	F	MP:0010506	prolonged RR interval	Golt1b<tm1b(EUCOMM)Wtsi>/Golt1b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Golt1b<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288485	F	MP:0000691	enlarged spleen	Golt1b<tm1b(EUCOMM)Wtsi>/Golt1b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Golt1b<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288485	F	MP:0000627	abnormal mammary gland morphology	Golt1b<tm1b(EUCOMM)Wtsi>/Golt1b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Golt1b<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288486	F	MP:0001566	increased circulating phosphate level	Gopc<tm1e.1(EUCOMM)Wtsi>/Gopc<+>	C57BL/6N-Gopc<tm1e.1(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288490	F	MP:0001399	hyperactivity	Gpr135<em1(IMPC)J>/Gpr135<em1(IMPC)J>	C57BL/6NJ-Gpr135<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288491	F	MP:0010511	shortened PR interval	Gpr150<em1(IMPC)J>/Gpr150<em1(IMPC)J>	C57BL/6NJ-Gpr150<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288491	F	MP:0002098	abnormal vibrissa morphology	Gpr150<em1(IMPC)J>/Gpr150<em1(IMPC)J>	C57BL/6NJ-Gpr150<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288493	M	MP:0001510	abnormal coat appearance	Gpr173<em1(IMPC)Bay>/Y	C57BL/6N-Gpr173<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288493	M	MP:0001399	hyperactivity	Gpr173<em1(IMPC)Bay>/Y	C57BL/6N-Gpr173<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288494	F	MP:0011239	abnormal skin coloration	Gpr173<em1(IMPC)Bay>/Gpr173<em1(IMPC)Bay>	C57BL/6N-Gpr173<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288495	M	MP:0011239	abnormal skin coloration	Gpr25<em1(IMPC)Bay>/Gpr25<em1(IMPC)Bay>	C57BL/6N-Gpr25<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288497	M	MP:0001399	hyperactivity	Gpr61<em1(IMPC)Bay>/Gpr61<em1(IMPC)Bay>	C57BL/6N-Gpr61<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288497	F	MP:0000063	decreased bone mineral density	Gpr61<em1(IMPC)Bay>/Gpr61<em1(IMPC)Bay>	C57BL/6N-Gpr61<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288500	F	MP:0004609	vertebral fusion	Gramd2a<em1(IMPC)Tcp>/Gramd2a<em1(IMPC)Tcp>	C57BL/6NCrl-Gramd2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288500	M	MP:0011874	enlarged urinary bladder	Gramd2a<em1(IMPC)Tcp>/Gramd2a<em1(IMPC)Tcp>	C57BL/6NCrl-Gramd2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288500	F	MP:0002637	small uterus	Gramd2a<em1(IMPC)Tcp>/Gramd2a<em1(IMPC)Tcp>	C57BL/6NCrl-Gramd2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288500	F	MP:0001944	abnormal pancreas morphology	Gramd2a<em1(IMPC)Tcp>/Gramd2a<em1(IMPC)Tcp>	C57BL/6NCrl-Gramd2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288500	M	MP:0000702	enlarged lymph nodes	Gramd2a<em1(IMPC)Tcp>/Gramd2a<em1(IMPC)Tcp>	C57BL/6NCrl-Gramd2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288500	M	MP:0000598	abnormal liver morphology	Gramd2a<em1(IMPC)Tcp>/Gramd2a<em1(IMPC)Tcp>	C57BL/6NCrl-Gramd2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288502	F	MP:0010124	decreased bone mineral content	Gria1<em1(IMPC)Hmgu>/Gria1<em1(IMPC)Hmgu>	C57BL/6N-Gria1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6288502	M	MP:0008806	increased circulating amylase level	Gria1<em1(IMPC)Hmgu>/Gria1<em1(IMPC)Hmgu>	C57BL/6N-Gria1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6288502	F	MP:0002757	decreased vertical activity	Gria1<em1(IMPC)Hmgu>/Gria1<em1(IMPC)Hmgu>	C57BL/6N-Gria1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6288502	F	MP:0009142	decreased prepulse inhibition	Gria1<em1(IMPC)Hmgu>/Gria1<em1(IMPC)Hmgu>	C57BL/6N-Gria1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6288502	M	MP:0001489	decreased startle reflex	Gria1<em1(IMPC)Hmgu>/Gria1<em1(IMPC)Hmgu>	C57BL/6N-Gria1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6288502	M	MP:0002968	increased circulating alkaline phosphatase level	Gria1<em1(IMPC)Hmgu>/Gria1<em1(IMPC)Hmgu>	C57BL/6N-Gria1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6288503	F	MP:0001402	decreased locomotor activity	Gstt1<tm1a(EUCOMM)Hmgu>/Gstt1<tm1a(EUCOMM)Hmgu>	C57BL/6N-Gstt1<tm1a(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288504	M	MP:0003896	prolonged PR interval	Gxylt1<em1(IMPC)Bay>/Gxylt1<+>	C57BL/6N-Gxylt1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288505	M	MP:0003232	abnormal forebrain development	Gxylt1<em1(IMPC)Bay>/Gxylt1<em1(IMPC)Bay>	C57BL/6N-Gxylt1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288505	M	MP:0001914	hemorrhage	Gxylt1<em1(IMPC)Bay>/Gxylt1<em1(IMPC)Bay>	C57BL/6N-Gxylt1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288505	M	MP:0001785	edema	Gxylt1<em1(IMPC)Bay>/Gxylt1<em1(IMPC)Bay>	C57BL/6N-Gxylt1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288505	M	MP:0002151	abnormal neural tube morphology	Gxylt1<em1(IMPC)Bay>/Gxylt1<em1(IMPC)Bay>	C57BL/6N-Gxylt1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288505	M	MP:0011100	preweaning lethality, complete penetrance	Gxylt1<em1(IMPC)Bay>/Gxylt1<em1(IMPC)Bay>	C57BL/6N-Gxylt1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288507	F	MP:0001392	abnormal locomotor behavior	Hcn1<em1(IMPC)H>/Hcn1<em1(IMPC)H>	C57BL/6N-Hcn1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288507	M	MP:0002833	increased heart weight	Hcn1<em1(IMPC)H>/Hcn1<em1(IMPC)H>	C57BL/6N-Hcn1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288508	M	MP:0002874	decreased hemoglobin content	Hddc2<em1(IMPC)H>/Hddc2<em1(IMPC)H>	C57BL/6NTac-Hddc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288508	M	MP:0005553	increased circulating creatinine level	Hddc2<em1(IMPC)H>/Hddc2<em1(IMPC)H>	C57BL/6NTac-Hddc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288508	M	MP:0001566	increased circulating phosphate level	Hddc2<em1(IMPC)H>/Hddc2<em1(IMPC)H>	C57BL/6NTac-Hddc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288508	M	MP:0002875	decreased erythrocyte cell number	Hddc2<em1(IMPC)H>/Hddc2<em1(IMPC)H>	C57BL/6NTac-Hddc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288508	M	MP:0005016	decreased lymphocyte cell number	Hddc2<em1(IMPC)H>/Hddc2<em1(IMPC)H>	C57BL/6NTac-Hddc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288508	F	MP:0002606	increased basophil cell number	Hddc2<em1(IMPC)H>/Hddc2<em1(IMPC)H>	C57BL/6NTac-Hddc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288508	M	MP:0000219	increased neutrophil cell number	Hddc2<em1(IMPC)H>/Hddc2<em1(IMPC)H>	C57BL/6NTac-Hddc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288508	M	MP:0005565	increased blood urea nitrogen level	Hddc2<em1(IMPC)H>/Hddc2<em1(IMPC)H>	C57BL/6NTac-Hddc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288508	M	MP:0010088	decreased circulating fructosamine level	Hddc2<em1(IMPC)H>/Hddc2<em1(IMPC)H>	C57BL/6NTac-Hddc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288508	F	MP:0001399	hyperactivity	Hddc2<em1(IMPC)H>/Hddc2<em1(IMPC)H>	C57BL/6NTac-Hddc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288508	M	MP:0005419	decreased circulating serum albumin level	Hddc2<em1(IMPC)H>/Hddc2<em1(IMPC)H>	C57BL/6NTac-Hddc2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288510	M	MP:0002764	short tibia	Hmmr<tm1b(EUCOMM)Hmgu>/Hmmr<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hmmr<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288510	M	MP:0000062	increased bone mineral density	Hmmr<tm1b(EUCOMM)Hmgu>/Hmmr<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hmmr<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288510	F	MP:0011110	preweaning lethality, incomplete penetrance	Hmmr<tm1b(EUCOMM)Hmgu>/Hmmr<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hmmr<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288512	M	MP:0000702	enlarged lymph nodes	Hook1<em1(IMPC)Tcp>/Hook1<em1(IMPC)Tcp>	C57BL/6NCrl-Hook1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288512	M	MP:0000692	small spleen	Hook1<em1(IMPC)Tcp>/Hook1<em1(IMPC)Tcp>	C57BL/6NCrl-Hook1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288512	M	MP:0001925	male infertility	Hook1<em1(IMPC)Tcp>/Hook1<em1(IMPC)Tcp>	C57BL/6NCrl-Hook1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288512	M	MP:0002060	abnormal skin morphology	Hook1<em1(IMPC)Tcp>/Hook1<em1(IMPC)Tcp>	C57BL/6NCrl-Hook1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288513	F	MP:0002075	abnormal coat/hair pigmentation	Hspb9<em1(IMPC)J>/Hspb9<em1(IMPC)J>	C57BL/6NJ-Hspb9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288513	F	MP:0001529	abnormal vocalization	Hspb9<em1(IMPC)J>/Hspb9<em1(IMPC)J>	C57BL/6NJ-Hspb9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288513	F	MP:0001399	hyperactivity	Hspb9<em1(IMPC)J>/Hspb9<em1(IMPC)J>	C57BL/6NJ-Hspb9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288514	M	MP:0004952	increased spleen weight	Hspbap1<tm1b(EUCOMM)Hmgu>/Hspbap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hspbap1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288514	M	MP:0003960	increased lean body mass	Hspbap1<tm1b(EUCOMM)Hmgu>/Hspbap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hspbap1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288514	M	MP:0010025	decreased total body fat amount	Hspbap1<tm1b(EUCOMM)Hmgu>/Hspbap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Hspbap1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288515	F	MP:0000689	abnormal spleen morphology	Idh3g<em1(IMPC)Bay>/Idh3g<em1(IMPC)Bay>	C57BL/6N-Idh3g<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288516	M	MP:0001325	abnormal retina morphology	Idi1<tm1b(EUCOMM)Hmgu>/Idi1<+>	C57BL/6N-Idi1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288516	M	MP:0010053	decreased grip strength	Idi1<tm1b(EUCOMM)Hmgu>/Idi1<+>	C57BL/6N-Idi1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288517	F	MP:0002060	abnormal skin morphology	Ifit3<em1(IMPC)Tcp>/Ifit3<em1(IMPC)Tcp>	C57BL/6NCrl-Ifit3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288517	F	MP:0000157	abnormal sternum morphology	Ifit3<em1(IMPC)Tcp>/Ifit3<em1(IMPC)Tcp>	C57BL/6NCrl-Ifit3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288517	M	MP:0000470	abnormal stomach morphology	Ifit3<em1(IMPC)Tcp>/Ifit3<em1(IMPC)Tcp>	C57BL/6NCrl-Ifit3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288518	F	MP:0009142	decreased prepulse inhibition	Ifng<tm1.1(KOMP)Vlcg>/Ifng<+>	C57BL/6N-Ifng<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288518	M	MP:0001175	abnormal lung morphology	Ifng<tm1.1(KOMP)Vlcg>/Ifng<+>	C57BL/6N-Ifng<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288518	M	MP:0002608	increased hematocrit	Ifng<tm1.1(KOMP)Vlcg>/Ifng<+>	C57BL/6N-Ifng<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288519	M	MP:0005178	increased circulating cholesterol level	Ift43<tm1b(EUCOMM)Hmgu>/Ift43<+>	C57BL/6N-Ift43<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288519	M	MP:0005568	increased circulating total protein level	Ift43<tm1b(EUCOMM)Hmgu>/Ift43<+>	C57BL/6N-Ift43<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288519	M	MP:0002965	increased circulating serum albumin level	Ift43<tm1b(EUCOMM)Hmgu>/Ift43<+>	C57BL/6N-Ift43<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288520	F	MP:0001319	irregularly shaped pupil	Igsf9b<em1(IMPC)J>/Igsf9b<em1(IMPC)J>	C57BL/6NJ-Igsf9b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288520	M	MP:0001415	increased exploration in new environment	Igsf9b<em1(IMPC)J>/Igsf9b<em1(IMPC)J>	C57BL/6NJ-Igsf9b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288523	F	MP:0005628	decreased circulating potassium level	Il4i1<tm1b(EUCOMM)Wtsi>/Il4i1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il4i1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288525	F	MP:0002875	decreased erythrocyte cell number	Inhbb<tm1b(EUCOMM)Hmgu>/Inhbb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Inhbb<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288525	F	MP:0002092	abnormal eye morphology	Inhbb<tm1b(EUCOMM)Hmgu>/Inhbb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Inhbb<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288525	M	MP:0001529	abnormal vocalization	Inhbb<tm1b(EUCOMM)Hmgu>/Inhbb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Inhbb<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288525	M	MP:0001523	impaired righting response	Inhbb<tm1b(EUCOMM)Hmgu>/Inhbb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Inhbb<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288525	M	MP:0001406	abnormal gait	Inhbb<tm1b(EUCOMM)Hmgu>/Inhbb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Inhbb<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288525	M	MP:0001392	abnormal locomotor behavior	Inhbb<tm1b(EUCOMM)Hmgu>/Inhbb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Inhbb<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288526	M	MP:0003960	increased lean body mass	Ino80d<tm1b(EUCOMM)Wtsi>/Ino80d<+>	C57BL/6N-Ino80d<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288526	M	MP:0010025	decreased total body fat amount	Ino80d<tm1b(EUCOMM)Wtsi>/Ino80d<+>	C57BL/6N-Ino80d<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288527	F	MP:0005655	increased aggression	Ints3<em1(IMPC)J>/Ints3<+>	C57BL/6NJ-Ints3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288527	F	MP:0001392	abnormal locomotor behavior	Ints3<em1(IMPC)J>/Ints3<+>	C57BL/6NJ-Ints3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288527	M	MP:0003131	increased erythrocyte cell number	Ints3<em1(IMPC)J>/Ints3<+>	C57BL/6NJ-Ints3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288527	M	MP:0002591	decreased mean corpuscular volume	Ints3<em1(IMPC)J>/Ints3<+>	C57BL/6NJ-Ints3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288527	F	MP:0010052	increased grip strength	Ints3<em1(IMPC)J>/Ints3<+>	C57BL/6NJ-Ints3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288528	M	MP:0000538	abnormal urinary bladder morphology	Ipo7<em1(IMPC)Mbp>/Ipo7<+>	C57BL/6N-Ipo7<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288528	F	MP:0000689	abnormal spleen morphology	Ipo7<em1(IMPC)Mbp>/Ipo7<+>	C57BL/6N-Ipo7<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288528	M	MP:0001552	increased circulating triglyceride level	Ipo7<em1(IMPC)Mbp>/Ipo7<+>	C57BL/6N-Ipo7<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288528	M	MP:0002079	increased circulating insulin level	Ipo7<em1(IMPC)Mbp>/Ipo7<+>	C57BL/6N-Ipo7<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288528	F	MP:0002282	abnormal trachea morphology	Ipo7<em1(IMPC)Mbp>/Ipo7<+>	C57BL/6N-Ipo7<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288528	F	MP:0001566	increased circulating phosphate level	Ipo7<em1(IMPC)Mbp>/Ipo7<+>	C57BL/6N-Ipo7<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288528	F	MP:0000702	enlarged lymph nodes	Ipo7<em1(IMPC)Mbp>/Ipo7<+>	C57BL/6N-Ipo7<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288528	F	MP:0000691	enlarged spleen	Ipo7<em1(IMPC)Mbp>/Ipo7<+>	C57BL/6N-Ipo7<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288528	F	MP:0002092	abnormal eye morphology	Ipo7<em1(IMPC)Mbp>/Ipo7<+>	C57BL/6N-Ipo7<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288528	F	MP:0001293	anophthalmia	Ipo7<em1(IMPC)Mbp>/Ipo7<+>	C57BL/6N-Ipo7<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288529	M	MP:0000274	enlarged heart	Ippk<tm1b(KOMP)Wtsi>/Ippk<+>	C57BL/6N-Ippk<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288529	M	MP:0000266	abnormal heart morphology	Ippk<tm1b(KOMP)Wtsi>/Ippk<+>	C57BL/6N-Ippk<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288531	M	MP:0010025	decreased total body fat amount	Iqcb1<em1(IMPC)Bay>/Iqcb1<+>	C57BL/6N-Iqcb1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288531	M	MP:0003960	increased lean body mass	Iqcb1<em1(IMPC)Bay>/Iqcb1<+>	C57BL/6N-Iqcb1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288531	F	MP:0011962	increased cornea thickness	Iqcb1<em1(IMPC)Bay>/Iqcb1<+>	C57BL/6N-Iqcb1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288531	M	MP:0002953	thick ventricular wall	Iqcb1<em1(IMPC)Bay>/Iqcb1<+>	C57BL/6N-Iqcb1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288531	M	MP:0010579	increased heart left ventricle size	Iqcb1<em1(IMPC)Bay>/Iqcb1<+>	C57BL/6N-Iqcb1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288533	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Itfg2<em1(IMPC)J>/Itfg2<+>	C57BL/6NJ-Itfg2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288534	F	MP:0005278	abnormal cholesterol homeostasis	Itm2c<em2(IMPC)Tcp>/Itm2c<em2(IMPC)Tcp>	C57BL/6NCrl-Itm2c<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288534	F	MP:0002764	short tibia	Itm2c<em2(IMPC)Tcp>/Itm2c<em2(IMPC)Tcp>	C57BL/6NCrl-Itm2c<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288535	M	MP:0004952	increased spleen weight	Junb<tm1b(EUCOMM)Hmgu>/Junb<+>	C57BL/6N-Junb<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288536	F	MP:0002092	abnormal eye morphology	Kat5<tm1.1(KOMP)Vlcg>/Kat5<+>	C57BL/6N-Kat5<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288538	F	MP:0010052	increased grip strength	Kcnc3<em1(IMPC)Bay>/Kcnc3<em1(IMPC)Bay>	C57BL/6N-Kcnc3<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288539	M	MP:0005140	decreased cardiac muscle contractility	Kcng2<em1(IMPC)Bay>/Kcng2<em1(IMPC)Bay>	C57BL/6N-Kcng2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288539	F	MP:0002833	increased heart weight	Kcng2<em1(IMPC)Bay>/Kcng2<em1(IMPC)Bay>	C57BL/6N-Kcng2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288539	M	MP:0011952	decreased cardiac stroke volume	Kcng2<em1(IMPC)Bay>/Kcng2<em1(IMPC)Bay>	C57BL/6N-Kcng2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288542	M	MP:0004222	iris synechia	Kcnv1<em1(IMPC)J>/Kcnv1<em1(IMPC)J>	C57BL/6NJ-Kcnv1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288542	M	MP:0001529	abnormal vocalization	Kcnv1<em1(IMPC)J>/Kcnv1<em1(IMPC)J>	C57BL/6NJ-Kcnv1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288543	F	MP:0003795	abnormal bone structure	Kdelr2<em1(IMPC)Bay>/Kdelr2<+>	C57BL/6N-Kdelr2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288548	M	MP:0002059	abnormal seminal vesicle morphology	Larp6<em1(IMPC)Tcp>/Larp6<em1(IMPC)Tcp>	C57BL/6NCrl-Larp6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288548	F	MP:0002968	increased circulating alkaline phosphatase level	Larp6<em1(IMPC)Tcp>/Larp6<em1(IMPC)Tcp>	C57BL/6NCrl-Larp6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288548	M	MP:0002092	abnormal eye morphology	Larp6<em1(IMPC)Tcp>/Larp6<em1(IMPC)Tcp>	C57BL/6NCrl-Larp6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288548	F	MP:0002060	abnormal skin morphology	Larp6<em1(IMPC)Tcp>/Larp6<em1(IMPC)Tcp>	C57BL/6NCrl-Larp6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288548	F	MP:0001552	increased circulating triglyceride level	Larp6<em1(IMPC)Tcp>/Larp6<em1(IMPC)Tcp>	C57BL/6NCrl-Larp6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288549	F	MP:0011959	abnormal eye posterior chamber depth	Lemd2<em1(IMPC)Bay>/Lemd2<+>	C57BL/6N-Lemd2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288549	F	MP:0000689	abnormal spleen morphology	Lemd2<em1(IMPC)Bay>/Lemd2<+>	C57BL/6N-Lemd2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288550	F	MP:0001510	abnormal coat appearance	Lep<tm1b(EUCOMM)Hmgu>/Lep<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lep<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288550	M	MP:0010392	prolonged QRS complex duration	Lep<tm1b(EUCOMM)Hmgu>/Lep<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lep<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288550	M	MP:0001925	male infertility	Lep<tm1b(EUCOMM)Hmgu>/Lep<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lep<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288550	F	MP:0001926	female infertility	Lep<tm1b(EUCOMM)Hmgu>/Lep<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lep<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288550	F	MP:0004953	decreased spleen weight	Lep<tm1b(EUCOMM)Hmgu>/Lep<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lep<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288550	M	MP:0011962	increased cornea thickness	Lep<tm1b(EUCOMM)Hmgu>/Lep<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lep<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288551	M	MP:0000689	abnormal spleen morphology	Lipt1<em1(IMPC)Bay>/Lipt1<+>	C57BL/6N-Lipt1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288554	M	MP:0001415	increased exploration in new environment	Lrrtm1<em1(IMPC)Mbp>/Lrrtm1<em1(IMPC)Mbp>	C57BL/6N-Lrrtm1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288554	M	MP:0004924	abnormal behavior	Lrrtm1<em1(IMPC)Mbp>/Lrrtm1<em1(IMPC)Mbp>	C57BL/6N-Lrrtm1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288554	M	MP:0002060	abnormal skin morphology	Lrrtm1<em1(IMPC)Mbp>/Lrrtm1<em1(IMPC)Mbp>	C57BL/6N-Lrrtm1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288554	M	MP:0020870	decreased thigmotaxis	Lrrtm1<em1(IMPC)Mbp>/Lrrtm1<em1(IMPC)Mbp>	C57BL/6N-Lrrtm1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288554	M	MP:0001364	decreased anxiety-related response	Lrrtm1<em1(IMPC)Mbp>/Lrrtm1<em1(IMPC)Mbp>	C57BL/6N-Lrrtm1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288554	F	MP:0002092	abnormal eye morphology	Lrrtm1<em1(IMPC)Mbp>/Lrrtm1<em1(IMPC)Mbp>	C57BL/6N-Lrrtm1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288554	M	MP:0001399	hyperactivity	Lrrtm1<em1(IMPC)Mbp>/Lrrtm1<em1(IMPC)Mbp>	C57BL/6N-Lrrtm1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288557	M	MP:0011110	preweaning lethality, incomplete penetrance	Lypla1<tm1b(EUCOMM)Hmgu>/Lypla1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Lypla1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288558	M	MP:0000266	abnormal heart morphology	Mab21l2<em1(IMPC)Mbp>/Mab21l2<em1(IMPC)Mbp>	C57BL/6N-Mab21l2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288559	F	MP:0002953	thick ventricular wall	Map3k12<tm1b(EUCOMM)Hmgu>/Map3k12<+>	C57BL/6N-Map3k12<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288559	F	MP:0010579	increased heart left ventricle size	Map3k12<tm1b(EUCOMM)Hmgu>/Map3k12<+>	C57BL/6N-Map3k12<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288560	F	MP:0001258	decreased body length	Map4k5<tm1b(EUCOMM)Hmgu>/Map4k5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Map4k5<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288560	F	MP:0002135	abnormal kidney morphology	Map4k5<tm1b(EUCOMM)Hmgu>/Map4k5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Map4k5<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288561	M	MP:0001146	abnormal testis morphology	Mark4<em1(IMPC)Mbp>/Mark4<em1(IMPC)Mbp>	C57BL/6N-Mark4<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288561	F	MP:0001297	microphthalmia	Mark4<em1(IMPC)Mbp>/Mark4<em1(IMPC)Mbp>	C57BL/6N-Mark4<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288561	M	MP:0000689	abnormal spleen morphology	Mark4<em1(IMPC)Mbp>/Mark4<em1(IMPC)Mbp>	C57BL/6N-Mark4<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288561	M	MP:0000691	enlarged spleen	Mark4<em1(IMPC)Mbp>/Mark4<em1(IMPC)Mbp>	C57BL/6N-Mark4<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288561	F	MP:0002574	increased vertical activity	Mark4<em1(IMPC)Mbp>/Mark4<em1(IMPC)Mbp>	C57BL/6N-Mark4<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288561	F	MP:0002092	abnormal eye morphology	Mark4<em1(IMPC)Mbp>/Mark4<em1(IMPC)Mbp>	C57BL/6N-Mark4<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288561	F	MP:0001120	abnormal uterus morphology	Mark4<em1(IMPC)Mbp>/Mark4<em1(IMPC)Mbp>	C57BL/6N-Mark4<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288561	M	MP:0001147	small testis	Mark4<em1(IMPC)Mbp>/Mark4<em1(IMPC)Mbp>	C57BL/6N-Mark4<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288561	M	MP:0002060	abnormal skin morphology	Mark4<em1(IMPC)Mbp>/Mark4<em1(IMPC)Mbp>	C57BL/6N-Mark4<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288563	M	MP:0001402	decreased locomotor activity	Mboat2<em1(IMPC)Mbp>/Mboat2<em1(IMPC)Mbp>	C57BL/6N-Mboat2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288563	M	MP:0002339	abnormal lymph node morphology	Mboat2<em1(IMPC)Mbp>/Mboat2<em1(IMPC)Mbp>	C57BL/6N-Mboat2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288563	F	MP:0000689	abnormal spleen morphology	Mboat2<em1(IMPC)Mbp>/Mboat2<em1(IMPC)Mbp>	C57BL/6N-Mboat2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288563	M	MP:0000702	enlarged lymph nodes	Mboat2<em1(IMPC)Mbp>/Mboat2<em1(IMPC)Mbp>	C57BL/6N-Mboat2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288563	F	MP:0000691	enlarged spleen	Mboat2<em1(IMPC)Mbp>/Mboat2<em1(IMPC)Mbp>	C57BL/6N-Mboat2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288563	M	MP:0020421	increased freezing behavior	Mboat2<em1(IMPC)Mbp>/Mboat2<em1(IMPC)Mbp>	C57BL/6N-Mboat2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288564	M	MP:0001697	abnormal embryo size	Mccc1<em1(IMPC)Bay>/Mccc1<em1(IMPC)Bay>	C57BL/6N-Mccc1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288565	M	MP:0002884	abnormal pharyngeal arch morphology	Mdh1<em1(IMPC)Bay>/Mdh1<em1(IMPC)Bay>	C57BL/6N-Mdh1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288567	M	MP:0005292	improved glucose tolerance	Me1<em1(IMPC)Tcp>/Me1<em1(IMPC)Tcp>	C57BL/6NCrl-Me1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288567	M	MP:0000702	enlarged lymph nodes	Me1<em1(IMPC)Tcp>/Me1<em1(IMPC)Tcp>	C57BL/6NCrl-Me1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288567	M	MP:0009142	decreased prepulse inhibition	Me1<em1(IMPC)Tcp>/Me1<em1(IMPC)Tcp>	C57BL/6NCrl-Me1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288567	M	MP:0002968	increased circulating alkaline phosphatase level	Me1<em1(IMPC)Tcp>/Me1<em1(IMPC)Tcp>	C57BL/6NCrl-Me1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288568	F	MP:0009709	hydrometra	Med1<tm3b(EUCOMM)Wtsi>/Med1<+>	C57BL/6N-Med1<tm3b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288568	F	MP:0004906	enlarged uterus	Med1<tm3b(EUCOMM)Wtsi>/Med1<+>	C57BL/6N-Med1<tm3b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288568	M	MP:0000266	abnormal heart morphology	Med1<tm3b(EUCOMM)Wtsi>/Med1<+>	C57BL/6N-Med1<tm3b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288568	F	MP:0002092	abnormal eye morphology	Med1<tm3b(EUCOMM)Wtsi>/Med1<+>	C57BL/6N-Med1<tm3b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288568	F	MP:0001102	small superior vagus ganglion	Med1<tm3b(EUCOMM)Wtsi>/Med1<+>	C57BL/6N-Med1<tm3b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288568	M	MP:0000274	enlarged heart	Med1<tm3b(EUCOMM)Wtsi>/Med1<+>	C57BL/6N-Med1<tm3b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288569	M	MP:0004258	abnormal placenta size	Med1<tm3b(EUCOMM)Wtsi>/Med1<tm3b(EUCOMM)Wtsi>	C57BL/6N-Med1<tm3b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288569	M	MP:0001722	pale yolk sac	Med1<tm3b(EUCOMM)Wtsi>/Med1<tm3b(EUCOMM)Wtsi>	C57BL/6N-Med1<tm3b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288570	M	MP:0010097	abnormal retina blood vessel morphology	Med27<em1(IMPC)Bay>/Med27<+>	C57BL/6N-Med27<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288572	F	MP:0010123	increased bone mineral content	Meis1<tm1b(EUCOMM)Hmgu>/Meis1<+>	C57BL/6N-Meis1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6288572	M	MP:0001399	hyperactivity	Meis1<tm1b(EUCOMM)Hmgu>/Meis1<+>	C57BL/6N-Meis1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6288576	F	MP:0002966	decreased circulating alkaline phosphatase level	Mfsd4b4<em1(IMPC)J>/Mfsd4b4<em1(IMPC)J>	C57BL/6NJ-Mfsd4b4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288576	M	MP:0001523	impaired righting response	Mfsd4b4<em1(IMPC)J>/Mfsd4b4<em1(IMPC)J>	C57BL/6NJ-Mfsd4b4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288577	M	MP:0011239	abnormal skin coloration	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288577	M	MP:0010124	decreased bone mineral content	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288577	M	MP:0000157	abnormal sternum morphology	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288577	M	MP:0002968	increased circulating alkaline phosphatase level	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288577	M	MP:0005561	increased mean corpuscular hemoglobin	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288577	F	MP:0002060	abnormal skin morphology	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288577	M	MP:0002075	abnormal coat/hair pigmentation	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288577	M	MP:0000186	decreased circulating HDL cholesterol level	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288577	M	MP:0002102	abnormal ear morphology	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288577	M	MP:0000702	enlarged lymph nodes	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288577	F	MP:0001944	abnormal pancreas morphology	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288577	M	MP:0000438	abnormal cranium morphology	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288577	M	MP:0005344	increased circulating bilirubin level	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288577	M	MP:0003795	abnormal bone structure	Mgrn1<em1(IMPC)Tcp>/Mgrn1<em1(IMPC)Tcp>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288578	M	MP:0002059	abnormal seminal vesicle morphology	Micu3<em1(IMPC)Mbp>/Micu3<em1(IMPC)Mbp>	C57BL/6N-Micu3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288578	F	MP:0003960	increased lean body mass	Micu3<em1(IMPC)Mbp>/Micu3<em1(IMPC)Mbp>	C57BL/6N-Micu3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288578	F	MP:0010025	decreased total body fat amount	Micu3<em1(IMPC)Mbp>/Micu3<em1(IMPC)Mbp>	C57BL/6N-Micu3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288578	M	MP:0003642	absent seminal vesicle	Micu3<em1(IMPC)Mbp>/Micu3<em1(IMPC)Mbp>	C57BL/6N-Micu3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288579	M	MP:0001146	abnormal testis morphology	Mpig6b<tm1.1(KOMP)Vlcg>/Mpig6b<tm1.1(KOMP)Vlcg>	C57BL/6N-Mpig6b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288579	F	MP:0003179	thrombocytopenia	Mpig6b<tm1.1(KOMP)Vlcg>/Mpig6b<tm1.1(KOMP)Vlcg>	C57BL/6N-Mpig6b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288579	F	MP:0002968	increased circulating alkaline phosphatase level	Mpig6b<tm1.1(KOMP)Vlcg>/Mpig6b<tm1.1(KOMP)Vlcg>	C57BL/6N-Mpig6b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288579	M	MP:0001147	small testis	Mpig6b<tm1.1(KOMP)Vlcg>/Mpig6b<tm1.1(KOMP)Vlcg>	C57BL/6N-Mpig6b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288579	F	MP:0000198	decreased circulating phosphate level	Mpig6b<tm1.1(KOMP)Vlcg>/Mpig6b<tm1.1(KOMP)Vlcg>	C57BL/6N-Mpig6b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288580	M	MP:0000598	abnormal liver morphology	Mrgprb2<em1(IMPC)Tcp>/Mrgprb2<em1(IMPC)Tcp>	C57BL/6NCrl-Mrgprb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288580	M	MP:0008528	polycystic kidney	Mrgprb2<em1(IMPC)Tcp>/Mrgprb2<em1(IMPC)Tcp>	C57BL/6NCrl-Mrgprb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288580	M	MP:0011874	enlarged urinary bladder	Mrgprb2<em1(IMPC)Tcp>/Mrgprb2<em1(IMPC)Tcp>	C57BL/6NCrl-Mrgprb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288580	F	MP:0001126	abnormal ovary morphology	Mrgprb2<em1(IMPC)Tcp>/Mrgprb2<em1(IMPC)Tcp>	C57BL/6NCrl-Mrgprb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288580	M	MP:0002060	abnormal skin morphology	Mrgprb2<em1(IMPC)Tcp>/Mrgprb2<em1(IMPC)Tcp>	C57BL/6NCrl-Mrgprb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288580	M	MP:0000692	small spleen	Mrgprb2<em1(IMPC)Tcp>/Mrgprb2<em1(IMPC)Tcp>	C57BL/6NCrl-Mrgprb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288580	M	MP:0002059	abnormal seminal vesicle morphology	Mrgprb2<em1(IMPC)Tcp>/Mrgprb2<em1(IMPC)Tcp>	C57BL/6NCrl-Mrgprb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288580	F	MP:0002989	small kidney	Mrgprb2<em1(IMPC)Tcp>/Mrgprb2<em1(IMPC)Tcp>	C57BL/6NCrl-Mrgprb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288580	M	MP:0002768	small adrenal glands	Mrgprb2<em1(IMPC)Tcp>/Mrgprb2<em1(IMPC)Tcp>	C57BL/6NCrl-Mrgprb2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288581	F	MP:0011100	preweaning lethality, complete penetrance	Mrm2<em1(IMPC)Bay>/Mrm2<em1(IMPC)Bay>	C57BL/6N-Mrm2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288583	M	MP:0011239	abnormal skin coloration	Msmb<tm1b(EUCOMM)Hmgu>/Msmb<tm1b(EUCOMM)Hmgu>	C57BL/6N-Msmb<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288586	F	MP:0010579	increased heart left ventricle size	Mthfd2<tm1b(EUCOMM)Wtsi>/Mthfd2<+>	C57BL/6N-Mthfd2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288586	F	MP:0010052	increased grip strength	Mthfd2<tm1b(EUCOMM)Wtsi>/Mthfd2<+>	C57BL/6N-Mthfd2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288587	F	MP:0005554	decreased circulating creatinine level	Mtpap<tm1.1(KOMP)Vlcg>/Mtpap<+>	C57BL/6N-Mtpap<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288587	F	MP:0000274	enlarged heart	Mtpap<tm1.1(KOMP)Vlcg>/Mtpap<+>	C57BL/6N-Mtpap<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288587	F	MP:0009709	hydrometra	Mtpap<tm1.1(KOMP)Vlcg>/Mtpap<+>	C57BL/6N-Mtpap<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288587	F	MP:0001102	small superior vagus ganglion	Mtpap<tm1.1(KOMP)Vlcg>/Mtpap<+>	C57BL/6N-Mtpap<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288587	F	MP:0000266	abnormal heart morphology	Mtpap<tm1.1(KOMP)Vlcg>/Mtpap<+>	C57BL/6N-Mtpap<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288590	F	MP:0001399	hyperactivity	Naa16<em1(IMPC)J>/Naa16<em1(IMPC)J>	C57BL/6NJ-Naa16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288590	M	MP:0000218	increased leukocyte cell number	Naa16<em1(IMPC)J>/Naa16<em1(IMPC)J>	C57BL/6NJ-Naa16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288592	M	MP:0010123	increased bone mineral content	Nadk<em2(IMPC)Bay>/Nadk<+>	C57BL/6N-Nadk<em2(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288592	M	MP:0003960	increased lean body mass	Nadk<em2(IMPC)Bay>/Nadk<+>	C57BL/6N-Nadk<em2(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288592	M	MP:0010025	decreased total body fat amount	Nadk<em2(IMPC)Bay>/Nadk<+>	C57BL/6N-Nadk<em2(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288594	M	MP:0001402	decreased locomotor activity	Napb<tm1b(EUCOMM)Hmgu>/Napb<+>	C57BL/6N-Napb<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288594	M	MP:0001364	decreased anxiety-related response	Napb<tm1b(EUCOMM)Hmgu>/Napb<+>	C57BL/6N-Napb<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288594	M	MP:0020870	decreased thigmotaxis	Napb<tm1b(EUCOMM)Hmgu>/Napb<+>	C57BL/6N-Napb<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288596	F	MP:0001297	microphthalmia	Nav3<em1(IMPC)Mbp>/Nav3<em1(IMPC)Mbp>	C57BL/6N-Nav3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288596	F	MP:0002092	abnormal eye morphology	Nav3<em1(IMPC)Mbp>/Nav3<em1(IMPC)Mbp>	C57BL/6N-Nav3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288598	F	MP:0005011	increased eosinophil cell number	Ncoa5<tm1.1(KOMP)Mbp>/Ncoa5<+>	C57BL/6N-Ncoa5<tm1.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288598	F	MP:0001102	small superior vagus ganglion	Ncoa5<tm1.1(KOMP)Mbp>/Ncoa5<+>	C57BL/6N-Ncoa5<tm1.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288598	M	MP:0000266	abnormal heart morphology	Ncoa5<tm1.1(KOMP)Mbp>/Ncoa5<+>	C57BL/6N-Ncoa5<tm1.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288598	M	MP:0000274	enlarged heart	Ncoa5<tm1.1(KOMP)Mbp>/Ncoa5<+>	C57BL/6N-Ncoa5<tm1.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288598	F	MP:0009709	hydrometra	Ncoa5<tm1.1(KOMP)Mbp>/Ncoa5<+>	C57BL/6N-Ncoa5<tm1.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288598	M	MP:0002833	increased heart weight	Ncoa5<tm1.1(KOMP)Mbp>/Ncoa5<+>	C57BL/6N-Ncoa5<tm1.1(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288601	F	MP:0010124	decreased bone mineral content	Nek1<em1(IMPC)Bay>/Nek1<em1(IMPC)Bay>	C57BL/6N-Nek1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288601	F	MP:0003795	abnormal bone structure	Nek1<em1(IMPC)Bay>/Nek1<em1(IMPC)Bay>	C57BL/6N-Nek1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288601	F	MP:0010053	decreased grip strength	Nek1<em1(IMPC)Bay>/Nek1<em1(IMPC)Bay>	C57BL/6N-Nek1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288601	M	MP:0002764	short tibia	Nek1<em1(IMPC)Bay>/Nek1<em1(IMPC)Bay>	C57BL/6N-Nek1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288601	F	MP:0003731	abnormal retina outer nuclear layer morphology	Nek1<em1(IMPC)Bay>/Nek1<em1(IMPC)Bay>	C57BL/6N-Nek1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288601	M	MP:0004509	abnormal pelvic girdle bone morphology	Nek1<em1(IMPC)Bay>/Nek1<em1(IMPC)Bay>	C57BL/6N-Nek1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288601	M	MP:0001925	male infertility	Nek1<em1(IMPC)Bay>/Nek1<em1(IMPC)Bay>	C57BL/6N-Nek1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288601	M	MP:0011952	decreased cardiac stroke volume	Nek1<em1(IMPC)Bay>/Nek1<em1(IMPC)Bay>	C57BL/6N-Nek1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288604	M	MP:0004952	increased spleen weight	Ngp<tm1b(KOMP)Wtsi>/Ngp<tm1b(KOMP)Wtsi>	C57BL/6N-Ngp<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288605	F	MP:0003984	embryonic growth retardation	Nmnat2<em1(IMPC)Mbp>/Nmnat2<em1(IMPC)Mbp>	C57BL/6N-Nmnat2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288605	F	MP:0001914	hemorrhage	Nmnat2<em1(IMPC)Mbp>/Nmnat2<em1(IMPC)Mbp>	C57BL/6N-Nmnat2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288605	F	MP:0001297	microphthalmia	Nmnat2<em1(IMPC)Mbp>/Nmnat2<em1(IMPC)Mbp>	C57BL/6N-Nmnat2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288606	F	MP:0011960	abnormal eye anterior chamber depth	Nos2<em1(IMPC)Bay>/Nos2<em1(IMPC)Bay>	C57BL/6N-Nos2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288607	M	MP:0005565	increased blood urea nitrogen level	Nos3<em1(IMPC)Mbp>/Nos3<em1(IMPC)Mbp>	C57BL/6N-Nos3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288607	M	MP:0000219	increased neutrophil cell number	Nos3<em1(IMPC)Mbp>/Nos3<em1(IMPC)Mbp>	C57BL/6N-Nos3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288607	M	MP:0002606	increased basophil cell number	Nos3<em1(IMPC)Mbp>/Nos3<em1(IMPC)Mbp>	C57BL/6N-Nos3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288607	M	MP:0000198	decreased circulating phosphate level	Nos3<em1(IMPC)Mbp>/Nos3<em1(IMPC)Mbp>	C57BL/6N-Nos3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288607	M	MP:0005016	decreased lymphocyte cell number	Nos3<em1(IMPC)Mbp>/Nos3<em1(IMPC)Mbp>	C57BL/6N-Nos3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288607	M	MP:0004931	enlarged epididymis	Nos3<em1(IMPC)Mbp>/Nos3<em1(IMPC)Mbp>	C57BL/6N-Nos3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288607	M	MP:0002631	abnormal epididymis morphology	Nos3<em1(IMPC)Mbp>/Nos3<em1(IMPC)Mbp>	C57BL/6N-Nos3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288608	F	MP:0001289	persistence of hyaloid vascular system	Nr2f1<tm1.1(KOMP)Mbp>/Nr2f1<+>	C57BL/6N-Nr2f1<tm1.1(KOMP)Mbp>/J	N	MGI:5576271
MGI:6288609	M	MP:0004924	abnormal behavior	Nrros<em1(IMPC)H>/Nrros<em1(IMPC)H>	C57BL/6N-Nrros<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288609	M	MP:0001513	limb grasping	Nrros<em1(IMPC)H>/Nrros<em1(IMPC)H>	C57BL/6N-Nrros<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288609	M	MP:0001363	increased anxiety-related response	Nrros<em1(IMPC)H>/Nrros<em1(IMPC)H>	C57BL/6N-Nrros<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288609	M	MP:0002797	increased thigmotaxis	Nrros<em1(IMPC)H>/Nrros<em1(IMPC)H>	C57BL/6N-Nrros<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288613	M	MP:0001284	absent vibrissae	Nup153<em1(IMPC)J>/Nup153<+>	C57BL/6NJ-Nup153<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288613	F	MP:0001399	hyperactivity	Nup153<em1(IMPC)J>/Nup153<+>	C57BL/6NJ-Nup153<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288613	F	MP:0002834	decreased heart weight	Nup153<em1(IMPC)J>/Nup153<+>	C57BL/6NJ-Nup153<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288614	M	MP:0009476	enlarged cecum	Nup35<tm1b(EUCOMM)Wtsi>/Nup35<+>	C57BL/6N-Nup35<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288614	M	MP:0010052	increased grip strength	Nup35<tm1b(EUCOMM)Wtsi>/Nup35<+>	C57BL/6N-Nup35<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288616	M	MP:0010025	decreased total body fat amount	Nup62<tm1b(KOMP)Wtsi>/Nup62<+>	C57BL/6N-Nup62<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288616	M	MP:0010123	increased bone mineral content	Nup62<tm1b(KOMP)Wtsi>/Nup62<+>	C57BL/6N-Nup62<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288616	F	MP:0003733	abnormal retina inner nuclear layer morphology	Nup62<tm1b(KOMP)Wtsi>/Nup62<+>	C57BL/6N-Nup62<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288617	M	MP:0010097	abnormal retina blood vessel morphology	Nxn<em1(IMPC)Bay>/Nxn<+>	C57BL/6N-Nxn<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288625	M	MP:0002941	increased circulating alanine transaminase level	P2ry14<em1(IMPC)H>/P2ry14<em1(IMPC)H>	C57BL/6NTac-P2ry14<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288625	M	MP:0005343	increased circulating aspartate transaminase level	P2ry14<em1(IMPC)H>/P2ry14<em1(IMPC)H>	C57BL/6NTac-P2ry14<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288625	M	MP:0010024	increased total body fat amount	P2ry14<em1(IMPC)H>/P2ry14<em1(IMPC)H>	C57BL/6NTac-P2ry14<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288626	M	MP:0002059	abnormal seminal vesicle morphology	Pacs1<em1(IMPC)Hmgu>/Pacs1<+>	C57BL/6N-Pacs1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6288628	M	MP:0000157	abnormal sternum morphology	Pah<em1(IMPC)Tcp>/Pah<em1(IMPC)Tcp>	C57BL/6NCrl-Pah<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288628	M	MP:0002075	abnormal coat/hair pigmentation	Pah<em1(IMPC)Tcp>/Pah<em1(IMPC)Tcp>	C57BL/6NCrl-Pah<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288628	M	MP:0002768	small adrenal glands	Pah<em1(IMPC)Tcp>/Pah<em1(IMPC)Tcp>	C57BL/6NCrl-Pah<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288628	M	MP:0001297	microphthalmia	Pah<em1(IMPC)Tcp>/Pah<em1(IMPC)Tcp>	C57BL/6NCrl-Pah<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288628	M	MP:0001312	abnormal cornea morphology	Pah<em1(IMPC)Tcp>/Pah<em1(IMPC)Tcp>	C57BL/6NCrl-Pah<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288628	F	MP:0001926	female infertility	Pah<em1(IMPC)Tcp>/Pah<em1(IMPC)Tcp>	C57BL/6NCrl-Pah<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288629	M	MP:0008806	increased circulating amylase level	Pak2<em1(IMPC)H>/Pak2<+>	C57BL/6NTac-Pak2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288629	M	MP:0002590	increased mean corpuscular volume	Pak2<em1(IMPC)H>/Pak2<+>	C57BL/6NTac-Pak2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288629	M	MP:0010506	prolonged RR interval	Pak2<em1(IMPC)H>/Pak2<+>	C57BL/6NTac-Pak2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288629	M	MP:0005561	increased mean corpuscular hemoglobin	Pak2<em1(IMPC)H>/Pak2<+>	C57BL/6NTac-Pak2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288631	M	MP:0011110	preweaning lethality, incomplete penetrance	Pak6<em1(IMPC)Bay>/Pak6<em1(IMPC)Bay>	C57BL/6N-Pak6<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288632	F	MP:0002574	increased vertical activity	Pak5<em1(IMPC)Mbp>/Pak5<em1(IMPC)Mbp>	C57BL/6N-Pak5<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288632	F	MP:0000702	enlarged lymph nodes	Pak5<em1(IMPC)Mbp>/Pak5<em1(IMPC)Mbp>	C57BL/6N-Pak5<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288632	F	MP:0002339	abnormal lymph node morphology	Pak5<em1(IMPC)Mbp>/Pak5<em1(IMPC)Mbp>	C57BL/6N-Pak5<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288633	F	MP:0001486	abnormal startle reflex	Palm3<tm1b(EUCOMM)Wtsi>/Palm3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Palm3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288634	F	MP:0001102	small superior vagus ganglion	Parg<tm2b(KOMP)Mbp>/Parg<+>	C57BL/6N-Parg<tm2b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288634	F	MP:0009709	hydrometra	Parg<tm2b(KOMP)Mbp>/Parg<+>	C57BL/6N-Parg<tm2b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288636	F	MP:0003864	abnormal midbrain development	Pcnp<em1(IMPC)Mbp>/Pcnp<em1(IMPC)Mbp>	C57BL/6N-Pcnp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288636	F	MP:0003720	abnormal neural tube closure	Pcnp<em1(IMPC)Mbp>/Pcnp<em1(IMPC)Mbp>	C57BL/6N-Pcnp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288636	F	MP:0009806	abnormal otic vesicle morphology	Pcnp<em1(IMPC)Mbp>/Pcnp<em1(IMPC)Mbp>	C57BL/6N-Pcnp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288636	F	MP:0003232	abnormal forebrain development	Pcnp<em1(IMPC)Mbp>/Pcnp<em1(IMPC)Mbp>	C57BL/6N-Pcnp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288640	F	MP:0002151	abnormal neural tube morphology	Pdhb<em1(IMPC)Bay>/Pdhb<em1(IMPC)Bay>	C57BL/6N-Pdhb<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288640	F	MP:0003984	embryonic growth retardation	Pdhb<em1(IMPC)Bay>/Pdhb<em1(IMPC)Bay>	C57BL/6N-Pdhb<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288640	F	MP:0001691	abnormal somite shape	Pdhb<em1(IMPC)Bay>/Pdhb<em1(IMPC)Bay>	C57BL/6N-Pdhb<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288640	M	MP:0011100	preweaning lethality, complete penetrance	Pdhb<em1(IMPC)Bay>/Pdhb<em1(IMPC)Bay>	C57BL/6N-Pdhb<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288640	F	MP:0002884	abnormal pharyngeal arch morphology	Pdhb<em1(IMPC)Bay>/Pdhb<em1(IMPC)Bay>	C57BL/6N-Pdhb<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288640	F	MP:0001700	abnormal embryo turning	Pdhb<em1(IMPC)Bay>/Pdhb<em1(IMPC)Bay>	C57BL/6N-Pdhb<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288642	M	MP:0005293	impaired glucose tolerance	Pdx1<tm1b(EUCOMM)Wtsi>/Pdx1<+>	C57BL/6N-Pdx1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288644	M	MP:0010024	increased total body fat amount	Pfdn5<tm1b(EUCOMM)Wtsi>/Pfdn5<+>	C57BL/6N-Pfdn5<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288644	M	MP:0003961	decreased lean body mass	Pfdn5<tm1b(EUCOMM)Wtsi>/Pfdn5<+>	C57BL/6N-Pfdn5<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288645	M	MP:0003179	thrombocytopenia	Phldb1<em1(IMPC)J>/Phldb1<em1(IMPC)J>	C57BL/6NJ-Phldb1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288645	F	MP:0001402	decreased locomotor activity	Phldb1<em1(IMPC)J>/Phldb1<em1(IMPC)J>	C57BL/6NJ-Phldb1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288645	F	MP:0010053	decreased grip strength	Phldb1<em1(IMPC)J>/Phldb1<em1(IMPC)J>	C57BL/6NJ-Phldb1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288645	F	MP:0001529	abnormal vocalization	Phldb1<em1(IMPC)J>/Phldb1<em1(IMPC)J>	C57BL/6NJ-Phldb1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288645	M	MP:0000063	decreased bone mineral density	Phldb1<em1(IMPC)J>/Phldb1<em1(IMPC)J>	C57BL/6NJ-Phldb1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288645	M	MP:0010124	decreased bone mineral content	Phldb1<em1(IMPC)J>/Phldb1<em1(IMPC)J>	C57BL/6NJ-Phldb1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288646	M	MP:0011965	decreased total retina thickness	Pigq<tm2b(EUCOMM)Wtsi>/Pigq<+>	C57BL/6N-Pigq<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288646	M	MP:0005293	impaired glucose tolerance	Pigq<tm2b(EUCOMM)Wtsi>/Pigq<+>	C57BL/6N-Pigq<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288646	F	MP:0003896	prolonged PR interval	Pigq<tm2b(EUCOMM)Wtsi>/Pigq<+>	C57BL/6N-Pigq<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288646	M	MP:0002792	abnormal retina vasculature morphology	Pigq<tm2b(EUCOMM)Wtsi>/Pigq<+>	C57BL/6N-Pigq<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288646	F	MP:0011960	abnormal eye anterior chamber depth	Pigq<tm2b(EUCOMM)Wtsi>/Pigq<+>	C57BL/6N-Pigq<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288647	M	MP:0000367	abnormal coat/ hair morphology	Pkmyt1<em1(IMPC)J>/Pkmyt1<+>	C57BL/6NJ-Pkmyt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288647	M	MP:0010052	increased grip strength	Pkmyt1<em1(IMPC)J>/Pkmyt1<+>	C57BL/6NJ-Pkmyt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288648	F	MP:0010052	increased grip strength	Pla2g4e<tm2b(EUCOMM)Hmgu>/Pla2g4e<tm2b(EUCOMM)Hmgu>	C57BL/6N-Pla2g4e<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288649	M	MP:0001925	male infertility	Pla2g6<tm1a(EUCOMM)Wtsi>/Pla2g6<tm1a(EUCOMM)Wtsi>	C57BL/6N-Pla2g6<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6288651	M	MP:0000538	abnormal urinary bladder morphology	Plod3<tm1.1(KOMP)Wtsi>/Plod3<+>	C57BL/6N-Plod3<tm1.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288655	F	MP:0000691	enlarged spleen	Pole2<em1(IMPC)Mbp>/Pole2<+>	C57BL/6NCrl-Pole2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288655	M	MP:0005293	impaired glucose tolerance	Pole2<em1(IMPC)Mbp>/Pole2<+>	C57BL/6NCrl-Pole2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288655	F	MP:0003720	abnormal neural tube closure	Pole2<em1(IMPC)Mbp>/Pole2<+>	C57BL/6NCrl-Pole2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288655	M	MP:0000598	abnormal liver morphology	Pole2<em1(IMPC)Mbp>/Pole2<+>	C57BL/6NCrl-Pole2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288655	M	MP:0001147	small testis	Pole2<em1(IMPC)Mbp>/Pole2<+>	C57BL/6NCrl-Pole2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288655	F	MP:0001297	microphthalmia	Pole2<em1(IMPC)Mbp>/Pole2<+>	C57BL/6NCrl-Pole2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288655	F	MP:0001120	abnormal uterus morphology	Pole2<em1(IMPC)Mbp>/Pole2<+>	C57BL/6NCrl-Pole2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288655	F	MP:0009141	increased prepulse inhibition	Pole2<em1(IMPC)Mbp>/Pole2<+>	C57BL/6NCrl-Pole2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288655	M	MP:0002997	enlarged seminal vesicle	Pole2<em1(IMPC)Mbp>/Pole2<+>	C57BL/6NCrl-Pole2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288655	M	MP:0003642	absent seminal vesicle	Pole2<em1(IMPC)Mbp>/Pole2<+>	C57BL/6NCrl-Pole2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288655	F	MP:0009084	blind uterus	Pole2<em1(IMPC)Mbp>/Pole2<+>	C57BL/6NCrl-Pole2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288655	F	MP:0003864	abnormal midbrain development	Pole2<em1(IMPC)Mbp>/Pole2<+>	C57BL/6NCrl-Pole2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288655	F	MP:0002060	abnormal skin morphology	Pole2<em1(IMPC)Mbp>/Pole2<+>	C57BL/6NCrl-Pole2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288660	F	MP:0000702	enlarged lymph nodes	Polrmt<em1(IMPC)Mbp>/Polrmt<+>	C57BL/6N-Polrmt<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288660	M	MP:0002152	abnormal brain morphology	Polrmt<em1(IMPC)Mbp>/Polrmt<+>	C57BL/6N-Polrmt<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288660	M	MP:0001891	hydrocephaly	Polrmt<em1(IMPC)Mbp>/Polrmt<+>	C57BL/6N-Polrmt<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288660	F	MP:0002339	abnormal lymph node morphology	Polrmt<em1(IMPC)Mbp>/Polrmt<+>	C57BL/6N-Polrmt<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288662	M	MP:0001529	abnormal vocalization	Ppfia3<em1(IMPC)J>/Ppfia3<em1(IMPC)J>	C57BL/6NJ-Ppfia3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288662	F	MP:0001319	irregularly shaped pupil	Ppfia3<em1(IMPC)J>/Ppfia3<em1(IMPC)J>	C57BL/6NJ-Ppfia3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288665	M	MP:0011962	increased cornea thickness	Ppp2cb<tm1b(EUCOMM)Hmgu>/Ppp2cb<+>	C57BL/6N-Ppp2cb<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288666	M	MP:0000702	enlarged lymph nodes	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	F	MP:0005179	decreased circulating cholesterol level	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	M	MP:0002339	abnormal lymph node morphology	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	F	MP:0010024	increased total body fat amount	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	F	MP:0002968	increased circulating alkaline phosphatase level	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	M	MP:0000691	enlarged spleen	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	M	MP:0005565	increased blood urea nitrogen level	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	M	MP:0010571	shortened ST segment	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	M	MP:0000689	abnormal spleen morphology	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	F	MP:0000219	increased neutrophil cell number	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	M	MP:0002833	increased heart weight	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	F	MP:0011110	preweaning lethality, incomplete penetrance	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	M	MP:0001489	decreased startle reflex	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	F	MP:0003961	decreased lean body mass	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	M	MP:0003900	shortened QT interval	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288666	F	MP:0000220	increased monocyte cell number	Ppp2r5c<em1(IMPC)Mbp>/Ppp2r5c<em1(IMPC)Mbp>	C57BL/6N-Ppp2r5c<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288668	M	MP:0001510	abnormal coat appearance	Pptc7<tm1b(EUCOMM)Hmgu>/Pptc7<+>	C57BL/6N-Pptc7<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288669	F	MP:0001417	decreased exploration in new environment	Pramel1<em1(IMPC)Tcp>/Pramel1<em1(IMPC)Tcp>	C57BL/6NCrl-Pramel1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288669	M	MP:0002941	increased circulating alanine transaminase level	Pramel1<em1(IMPC)Tcp>/Pramel1<em1(IMPC)Tcp>	C57BL/6NCrl-Pramel1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288669	M	MP:0002059	abnormal seminal vesicle morphology	Pramel1<em1(IMPC)Tcp>/Pramel1<em1(IMPC)Tcp>	C57BL/6NCrl-Pramel1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288669	F	MP:0002060	abnormal skin morphology	Pramel1<em1(IMPC)Tcp>/Pramel1<em1(IMPC)Tcp>	C57BL/6NCrl-Pramel1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288669	M	MP:0003068	enlarged kidney	Pramel1<em1(IMPC)Tcp>/Pramel1<em1(IMPC)Tcp>	C57BL/6NCrl-Pramel1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288669	M	MP:0011874	enlarged urinary bladder	Pramel1<em1(IMPC)Tcp>/Pramel1<em1(IMPC)Tcp>	C57BL/6NCrl-Pramel1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288669	M	MP:0000702	enlarged lymph nodes	Pramel1<em1(IMPC)Tcp>/Pramel1<em1(IMPC)Tcp>	C57BL/6NCrl-Pramel1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288670	F	MP:0003795	abnormal bone structure	Prdm14<em1(IMPC)Bay>/Prdm14<em1(IMPC)Bay>	C57BL/6N-Prdm14<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288670	F	MP:0003961	decreased lean body mass	Prdm14<em1(IMPC)Bay>/Prdm14<em1(IMPC)Bay>	C57BL/6N-Prdm14<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288670	F	MP:0000063	decreased bone mineral density	Prdm14<em1(IMPC)Bay>/Prdm14<em1(IMPC)Bay>	C57BL/6N-Prdm14<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288670	F	MP:0011110	preweaning lethality, incomplete penetrance	Prdm14<em1(IMPC)Bay>/Prdm14<em1(IMPC)Bay>	C57BL/6N-Prdm14<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288670	F	MP:0010024	increased total body fat amount	Prdm14<em1(IMPC)Bay>/Prdm14<em1(IMPC)Bay>	C57BL/6N-Prdm14<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288670	F	MP:0011960	abnormal eye anterior chamber depth	Prdm14<em1(IMPC)Bay>/Prdm14<em1(IMPC)Bay>	C57BL/6N-Prdm14<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288670	F	MP:0010124	decreased bone mineral content	Prdm14<em1(IMPC)Bay>/Prdm14<em1(IMPC)Bay>	C57BL/6N-Prdm14<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288671	F	MP:0011959	abnormal eye posterior chamber depth	Prg2<tm1b(EUCOMM)Hmgu>/Prg2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prg2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288671	M	MP:0001510	abnormal coat appearance	Prg2<tm1b(EUCOMM)Hmgu>/Prg2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prg2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288671	F	MP:0010378	increased respiratory quotient	Prg2<tm1b(EUCOMM)Hmgu>/Prg2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prg2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288672	F	MP:0004952	increased spleen weight	Prkab1<em1(IMPC)Bay>/Prkab1<em1(IMPC)Bay>	C57BL/6N-Prkab1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288673	M	MP:0020870	decreased thigmotaxis	Prkag2<em1(IMPC)J>/Prkag2<em1(IMPC)J>	C57BL/6NJ-Prkag2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288673	M	MP:0001417	decreased exploration in new environment	Prkag2<em1(IMPC)J>/Prkag2<em1(IMPC)J>	C57BL/6NJ-Prkag2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288674	F	MP:0010053	decreased grip strength	Prkch<tm1b(EUCOMM)Hmgu>/Prkch<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Prkch<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6288674	M	MP:0003960	increased lean body mass	Prkch<tm1b(EUCOMM)Hmgu>/Prkch<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Prkch<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6288675	M	MP:0011940	decreased food intake	Prkd2<em1(IMPC)Hmgu>/Prkd2<em1(IMPC)Hmgu>	C57BL/6N-Prkd2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6288675	M	MP:0010379	decreased respiratory quotient	Prkd2<em1(IMPC)Hmgu>/Prkd2<em1(IMPC)Hmgu>	C57BL/6N-Prkd2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6288675	F	MP:0001289	persistence of hyaloid vascular system	Prkd2<em1(IMPC)Hmgu>/Prkd2<em1(IMPC)Hmgu>	C57BL/6N-Prkd2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6288675	M	MP:0002152	abnormal brain morphology	Prkd2<em1(IMPC)Hmgu>/Prkd2<em1(IMPC)Hmgu>	C57BL/6N-Prkd2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6288676	M	MP:0010052	increased grip strength	Prmt9<em1(IMPC)J>/Prmt9<em1(IMPC)J>	C57BL/6NJ-Prmt9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288676	M	MP:0005561	increased mean corpuscular hemoglobin	Prmt9<em1(IMPC)J>/Prmt9<em1(IMPC)J>	C57BL/6NJ-Prmt9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288677	M	MP:0009476	enlarged cecum	Prox2<em1(IMPC)Hmgu>/Prox2<em1(IMPC)Hmgu>	C57BL/6N-Prox2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6288678	F	MP:0001399	hyperactivity	Prrc2c<em1(IMPC)J>/Prrc2c<+>	C57BL/6NJ-Prrc2c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288678	M	MP:0000367	abnormal coat/ hair morphology	Prrc2c<em1(IMPC)J>/Prrc2c<+>	C57BL/6NJ-Prrc2c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288681	F	MP:0001399	hyperactivity	Psmg1<tm1b(KOMP)Wtsi>/Psmg1<+>	C57BL/6N-Psmg1<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288682	F	MP:0001926	female infertility	Ptger2<tm1.1(KOMP)Vlcg>/Ptger2<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptger2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288682	M	MP:0001925	male infertility	Ptger2<tm1.1(KOMP)Vlcg>/Ptger2<tm1.1(KOMP)Vlcg>	C57BL/6N-Ptger2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6288683	M	MP:0001289	persistence of hyaloid vascular system	Pygo2<tm1b(EUCOMM)Wtsi>/Pygo2<+>	C57BL/6N-Pygo2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288683	F	MP:0009709	hydrometra	Pygo2<tm1b(EUCOMM)Wtsi>/Pygo2<+>	C57BL/6N-Pygo2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288683	F	MP:0002135	abnormal kidney morphology	Pygo2<tm1b(EUCOMM)Wtsi>/Pygo2<+>	C57BL/6N-Pygo2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288683	F	MP:0001120	abnormal uterus morphology	Pygo2<tm1b(EUCOMM)Wtsi>/Pygo2<+>	C57BL/6N-Pygo2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288684	M	MP:0002092	abnormal eye morphology	Pygo2<tm1b(EUCOMM)Wtsi>/Pygo2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pygo2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288684	M	MP:0003720	abnormal neural tube closure	Pygo2<tm1b(EUCOMM)Wtsi>/Pygo2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pygo2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288684	M	MP:0000897	abnormal midbrain morphology	Pygo2<tm1b(EUCOMM)Wtsi>/Pygo2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pygo2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288684	F	MP:0000428	abnormal craniofacial morphology	Pygo2<tm1b(EUCOMM)Wtsi>/Pygo2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pygo2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288684	M	MP:0000841	abnormal hindbrain morphology	Pygo2<tm1b(EUCOMM)Wtsi>/Pygo2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pygo2<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6288685	F	MP:0001488	increased startle reflex	Rab10<em1(IMPC)J>/Rab10<+>	C57BL/6NJ-Rab10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288686	M	MP:0000598	abnormal liver morphology	Rac2<em1(IMPC)Mbp>/Rac2<em1(IMPC)Mbp>	C57BL/6N-Rac2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288687	F	MP:0012121	sclerocornea	Rad54l<em1Murr>/Rad54l<+>	C57BL/6N-Rad54l<em1Murr>/MurrJ	N	MGI:5576271
MGI:6288688	F	MP:0001697	abnormal embryo size	Ranbp1<tm1b(KOMP)Wtsi>/Ranbp1<tm1b(KOMP)Wtsi>	C57BL/6N-Ranbp1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288688	F	MP:0004258	abnormal placenta size	Ranbp1<tm1b(KOMP)Wtsi>/Ranbp1<tm1b(KOMP)Wtsi>	C57BL/6N-Ranbp1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288689	M	MP:0005016	decreased lymphocyte cell number	Rap1gap<em1(IMPC)H>/Rap1gap<em1(IMPC)H>	C57BL/6NTac-Rap1gap<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288689	F	MP:0008806	increased circulating amylase level	Rap1gap<em1(IMPC)H>/Rap1gap<em1(IMPC)H>	C57BL/6NTac-Rap1gap<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288689	M	MP:0010067	increased red blood cell distribution width	Rap1gap<em1(IMPC)H>/Rap1gap<em1(IMPC)H>	C57BL/6NTac-Rap1gap<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288689	F	MP:0005011	increased eosinophil cell number	Rap1gap<em1(IMPC)H>/Rap1gap<em1(IMPC)H>	C57BL/6NTac-Rap1gap<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288689	M	MP:0000219	increased neutrophil cell number	Rap1gap<em1(IMPC)H>/Rap1gap<em1(IMPC)H>	C57BL/6NTac-Rap1gap<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288692	M	MP:0002574	increased vertical activity	Rnf10<em1(IMPC)Bay>/Rnf10<em1(IMPC)Bay>	C57BL/6N-Rnf10<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288692	F	MP:0010097	abnormal retina blood vessel morphology	Rnf10<em1(IMPC)Bay>/Rnf10<em1(IMPC)Bay>	C57BL/6N-Rnf10<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288692	F	MP:0011965	decreased total retina thickness	Rnf10<em1(IMPC)Bay>/Rnf10<em1(IMPC)Bay>	C57BL/6N-Rnf10<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288692	F	MP:0009142	decreased prepulse inhibition	Rnf10<em1(IMPC)Bay>/Rnf10<em1(IMPC)Bay>	C57BL/6N-Rnf10<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288693	F	MP:0001566	increased circulating phosphate level	Rnf214<em1(IMPC)J>/Rnf214<em1(IMPC)J>	C57BL/6NJ-Rnf214<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288693	F	MP:0005562	decreased mean corpuscular hemoglobin	Rnf214<em1(IMPC)J>/Rnf214<em1(IMPC)J>	C57BL/6NJ-Rnf214<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288693	F	MP:0000194	increased circulating calcium level	Rnf214<em1(IMPC)J>/Rnf214<em1(IMPC)J>	C57BL/6NJ-Rnf214<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288694	M	MP:0002833	increased heart weight	Rnf31<tm1b(KOMP)Wtsi>/Rnf31<+>	C57BL/6N-Rnf31<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288694	F	MP:0000266	abnormal heart morphology	Rnf31<tm1b(KOMP)Wtsi>/Rnf31<+>	C57BL/6N-Rnf31<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288694	M	MP:0001257	increased body length	Rnf31<tm1b(KOMP)Wtsi>/Rnf31<+>	C57BL/6N-Rnf31<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288694	F	MP:0000274	enlarged heart	Rnf31<tm1b(KOMP)Wtsi>/Rnf31<+>	C57BL/6N-Rnf31<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288695	M	MP:0001697	abnormal embryo size	Rnf31<tm1b(KOMP)Wtsi>/Rnf31<tm1b(KOMP)Wtsi>	C57BL/6N-Rnf31<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6288696	M	MP:0000689	abnormal spleen morphology	Rnft2<tm1b(EUCOMM)Hmgu>/Rnft2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rnft2<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288702	M	MP:0000367	abnormal coat/ hair morphology	Rpl7l1<tm2b(EUCOMM)Hmgu>/Rpl7l1<+>	C57BL/6N-Rpl7l1<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288702	M	MP:0001510	abnormal coat appearance	Rpl7l1<tm2b(EUCOMM)Hmgu>/Rpl7l1<+>	C57BL/6N-Rpl7l1<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288702	F	MP:0011960	abnormal eye anterior chamber depth	Rpl7l1<tm2b(EUCOMM)Hmgu>/Rpl7l1<+>	C57BL/6N-Rpl7l1<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288703	F	MP:0011960	abnormal eye anterior chamber depth	Rps6kc1<tm1b(EUCOMM)Wtsi>/Rps6kc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rps6kc1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288704	M	MP:0004952	increased spleen weight	Rpusd2<tm1b(KOMP)Wtsi>/Rpusd2<tm1b(KOMP)Wtsi>	C57BL/6N-Rpusd2<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288706	M	MP:0005534	decreased body temperature	Rrp1<em1(IMPC)Bay>/Rrp1<+>	C57BL/6N-Rrp1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288710	F	MP:0010052	increased grip strength	Rxylt1<em1(IMPC)J>/Rxylt1<+>	C57BL/6N-Rxylt1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6288710	F	MP:0001399	hyperactivity	Rxylt1<em1(IMPC)J>/Rxylt1<+>	C57BL/6N-Rxylt1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6288712	F	MP:0010123	increased bone mineral content	Sash1<em1(IMPC)Bay>/Sash1<+>	C57BL/6N-Sash1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288712	F	MP:0002792	abnormal retina vasculature morphology	Sash1<em1(IMPC)Bay>/Sash1<+>	C57BL/6N-Sash1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288713	M	MP:0003984	embryonic growth retardation	Sash1<em1(IMPC)Bay>/Sash1<em1(IMPC)Bay>	C57BL/6N-Sash1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288714	M	MP:0001510	abnormal coat appearance	Sbk1<tm1b(EUCOMM)Wtsi>/Sbk1<+>	C57BL/6N-Sbk1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288714	F	MP:0011960	abnormal eye anterior chamber depth	Sbk1<tm1b(EUCOMM)Wtsi>/Sbk1<+>	C57BL/6N-Sbk1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288714	F	MP:0011965	decreased total retina thickness	Sbk1<tm1b(EUCOMM)Wtsi>/Sbk1<+>	C57BL/6N-Sbk1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288715	M	MP:0005419	decreased circulating serum albumin level	Sbk2<em1(IMPC)Bay>/Sbk2<em1(IMPC)Bay>	C57BL/6N-Sbk2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288719	F	MP:0001417	decreased exploration in new environment	Sertad3<em1(IMPC)Tcp>/Sertad3<em1(IMPC)Tcp>	C57BL/6NCrl-Sertad3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288720	F	MP:0006108	abnormal hindbrain development	Sfmbt2<em1(IMPC)Mbp>/Sfmbt2<em1(IMPC)Mbp>	C57BL/6NCrl-Sfmbt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288720	F	MP:0001700	abnormal embryo turning	Sfmbt2<em1(IMPC)Mbp>/Sfmbt2<em1(IMPC)Mbp>	C57BL/6NCrl-Sfmbt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288720	F	MP:0003720	abnormal neural tube closure	Sfmbt2<em1(IMPC)Mbp>/Sfmbt2<em1(IMPC)Mbp>	C57BL/6NCrl-Sfmbt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288721	M	MP:0001417	decreased exploration in new environment	Sh3rf1<em1(IMPC)J>/Sh3rf1<em1(IMPC)J>	C57BL/6NJ-Sh3rf1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288724	F	MP:0010579	increased heart left ventricle size	Slc10a2<tm1b(KOMP)Mbp>/Slc10a2<tm1b(KOMP)Mbp>	C57BL/6N-Slc10a2<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6288725	F	MP:0011110	preweaning lethality, incomplete penetrance	Slc10a4<tm1b(KOMP)Wtsi>/Slc10a4<tm1b(KOMP)Wtsi>	C57BL/6N-Slc10a4<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288725	F	MP:0020870	decreased thigmotaxis	Slc10a4<tm1b(KOMP)Wtsi>/Slc10a4<tm1b(KOMP)Wtsi>	C57BL/6N-Slc10a4<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288727	F	MP:0001415	increased exploration in new environment	Slc25a1<tm1b(EUCOMM)Wtsi>/Slc25a1<+>	C57BL/6N-Slc25a1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288728	F	MP:0010052	increased grip strength	Slc25a24<tm1b(KOMP)Wtsi>/Slc25a24<tm1b(KOMP)Wtsi>	C57BL/6N-Slc25a24<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288729	M	MP:0000706	small thymus	Slc30a4<em1(IMPC)Tcp>/Slc30a4<em1(IMPC)Tcp>	C57BL/6NCrl-Slc30a4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288729	M	MP:0002060	abnormal skin morphology	Slc30a4<em1(IMPC)Tcp>/Slc30a4<em1(IMPC)Tcp>	C57BL/6NCrl-Slc30a4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288729	M	MP:0002768	small adrenal glands	Slc30a4<em1(IMPC)Tcp>/Slc30a4<em1(IMPC)Tcp>	C57BL/6NCrl-Slc30a4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288729	F	MP:0010052	increased grip strength	Slc30a4<em1(IMPC)Tcp>/Slc30a4<em1(IMPC)Tcp>	C57BL/6NCrl-Slc30a4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288729	M	MP:0003068	enlarged kidney	Slc30a4<em1(IMPC)Tcp>/Slc30a4<em1(IMPC)Tcp>	C57BL/6NCrl-Slc30a4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288729	F	MP:0001126	abnormal ovary morphology	Slc30a4<em1(IMPC)Tcp>/Slc30a4<em1(IMPC)Tcp>	C57BL/6NCrl-Slc30a4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288729	F	MP:0010053	decreased grip strength	Slc30a4<em1(IMPC)Tcp>/Slc30a4<em1(IMPC)Tcp>	C57BL/6NCrl-Slc30a4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288730	M	MP:0001510	abnormal coat appearance	Slc35d1<tm2b(EUCOMM)Hmgu>/Slc35d1<+>	C57BL/6N-Slc35d1<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288731	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Slc9a5<em1(IMPC)J>/Slc9a5<em1(IMPC)J>	C57BL/6NJ-Slc9a5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288732	F	MP:0001120	abnormal uterus morphology	Slitrk2<em1(IMPC)Mbp>/Slitrk2<em1(IMPC)Mbp>	C57BL/6NCrl-Slitrk2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288732	F	MP:0004832	enlarged ovary	Slitrk2<em1(IMPC)Mbp>/Slitrk2<em1(IMPC)Mbp>	C57BL/6NCrl-Slitrk2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288732	F	MP:0001126	abnormal ovary morphology	Slitrk2<em1(IMPC)Mbp>/Slitrk2<em1(IMPC)Mbp>	C57BL/6NCrl-Slitrk2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288732	F	MP:0001415	increased exploration in new environment	Slitrk2<em1(IMPC)Mbp>/Slitrk2<em1(IMPC)Mbp>	C57BL/6NCrl-Slitrk2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288732	F	MP:0004906	enlarged uterus	Slitrk2<em1(IMPC)Mbp>/Slitrk2<em1(IMPC)Mbp>	C57BL/6NCrl-Slitrk2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288734	M	MP:0003960	increased lean body mass	Smagp<tm1b(KOMP)Mbp>/Smagp<tm1b(KOMP)Mbp>	C57BL/6N-Smagp<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6288735	M	MP:0001510	abnormal coat appearance	Smarcb1<tm1b(EUCOMM)Hmgu>/Smarcb1<+>	C57BL/6N-Smarcb1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288735	F	MP:0009142	decreased prepulse inhibition	Smarcb1<tm1b(EUCOMM)Hmgu>/Smarcb1<+>	C57BL/6N-Smarcb1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288738	M	MP:0009142	decreased prepulse inhibition	Snx14<em1(IMPC)H>/Snx14<+>	C57BL/6NTac-Snx14<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288738	M	MP:0002599	increased mean platelet volume	Snx14<em1(IMPC)H>/Snx14<+>	C57BL/6NTac-Snx14<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288738	M	MP:0010052	increased grip strength	Snx14<em1(IMPC)H>/Snx14<+>	C57BL/6NTac-Snx14<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288743	M	MP:0005011	increased eosinophil cell number	Spns3<em1(IMPC)Tcp>/Spns3<em1(IMPC)Tcp>	C57BL/6NCrl-Spns3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288743	M	MP:0000157	abnormal sternum morphology	Spns3<em1(IMPC)Tcp>/Spns3<em1(IMPC)Tcp>	C57BL/6NCrl-Spns3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288743	M	MP:0010067	increased red blood cell distribution width	Spns3<em1(IMPC)Tcp>/Spns3<em1(IMPC)Tcp>	C57BL/6NCrl-Spns3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288743	M	MP:0003068	enlarged kidney	Spns3<em1(IMPC)Tcp>/Spns3<em1(IMPC)Tcp>	C57BL/6NCrl-Spns3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288743	F	MP:0001120	abnormal uterus morphology	Spns3<em1(IMPC)Tcp>/Spns3<em1(IMPC)Tcp>	C57BL/6NCrl-Spns3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288743	M	MP:0011874	enlarged urinary bladder	Spns3<em1(IMPC)Tcp>/Spns3<em1(IMPC)Tcp>	C57BL/6NCrl-Spns3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288746	F	MP:0005385	cardiovascular system phenotype	Srsf11<tm1b(EUCOMM)Wtsi>/Srsf11<+>	C57BL/6N-Srsf11<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288746	F	MP:0003928	increased heart rate variability	Srsf11<tm1b(EUCOMM)Wtsi>/Srsf11<+>	C57BL/6N-Srsf11<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288747	F	MP:0010053	decreased grip strength	Stx1a<tm1b(EUCOMM)Hmgu>/Stx1a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Stx1a<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288747	M	MP:0011965	decreased total retina thickness	Stx1a<tm1b(EUCOMM)Hmgu>/Stx1a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Stx1a<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288749	M	MP:0002626	increased heart rate	Synrg<tm1b(EUCOMM)Wtsi>/Synrg<+>	C57BL/6N-Synrg<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288751	F	MP:0005554	decreased circulating creatinine level	Taco1<em1(IMPC)J>/Taco1<em1(IMPC)J>	C57BL/6NJ-Taco1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288751	M	MP:0004222	iris synechia	Taco1<em1(IMPC)J>/Taco1<em1(IMPC)J>	C57BL/6NJ-Taco1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288751	M	MP:0002833	increased heart weight	Taco1<em1(IMPC)J>/Taco1<em1(IMPC)J>	C57BL/6NJ-Taco1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288751	M	MP:0002644	decreased circulating triglyceride level	Taco1<em1(IMPC)J>/Taco1<em1(IMPC)J>	C57BL/6NJ-Taco1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288751	F	MP:0002060	abnormal skin morphology	Taco1<em1(IMPC)J>/Taco1<em1(IMPC)J>	C57BL/6NJ-Taco1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288753	F	MP:0002092	abnormal eye morphology	Tafa3<em1(IMPC)Mbp>/Tafa3<em1(IMPC)Mbp>	C57BL/6N-Tafa3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288753	F	MP:0003795	abnormal bone structure	Tafa3<em1(IMPC)Mbp>/Tafa3<em1(IMPC)Mbp>	C57BL/6N-Tafa3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288754	F	MP:0000639	abnormal adrenal gland morphology	Tas2r102<em1(IMPC)Bay>/Tas2r102<em1(IMPC)Bay>	C57BL/6N-Tas2r102<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288757	M	MP:0011239	abnormal skin coloration	Tas2r131<em1(IMPC)Bay>/Tas2r131<em1(IMPC)Bay>	C57BL/6N-Tas2r131<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288757	M	MP:0000689	abnormal spleen morphology	Tas2r131<em1(IMPC)Bay>/Tas2r131<em1(IMPC)Bay>	C57BL/6N-Tas2r131<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288762	M	MP:0005565	increased blood urea nitrogen level	Tbl1xr1<tm1b(EUCOMM)Hmgu>/Tbl1xr1<+>	C57BL/6N-Tbl1xr1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288762	F	MP:0000598	abnormal liver morphology	Tbl1xr1<tm1b(EUCOMM)Hmgu>/Tbl1xr1<+>	C57BL/6N-Tbl1xr1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288762	F	MP:0004832	enlarged ovary	Tbl1xr1<tm1b(EUCOMM)Hmgu>/Tbl1xr1<+>	C57BL/6N-Tbl1xr1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288762	M	MP:0000599	enlarged liver	Tbl1xr1<tm1b(EUCOMM)Hmgu>/Tbl1xr1<+>	C57BL/6N-Tbl1xr1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288762	F	MP:0001284	absent vibrissae	Tbl1xr1<tm1b(EUCOMM)Hmgu>/Tbl1xr1<+>	C57BL/6N-Tbl1xr1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288762	M	MP:0009476	enlarged cecum	Tbl1xr1<tm1b(EUCOMM)Hmgu>/Tbl1xr1<+>	C57BL/6N-Tbl1xr1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6288764	F	MP:0002989	small kidney	Tceal1<em1(IMPC)Tcp>/Tceal1<em1(IMPC)Tcp>	C57BL/6NCrl-Tceal1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288764	F	MP:0002092	abnormal eye morphology	Tceal1<em1(IMPC)Tcp>/Tceal1<em1(IMPC)Tcp>	C57BL/6NCrl-Tceal1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288764	F	MP:0010024	increased total body fat amount	Tceal1<em1(IMPC)Tcp>/Tceal1<em1(IMPC)Tcp>	C57BL/6NCrl-Tceal1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288764	F	MP:0003961	decreased lean body mass	Tceal1<em1(IMPC)Tcp>/Tceal1<em1(IMPC)Tcp>	C57BL/6NCrl-Tceal1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288765	F	MP:0009709	hydrometra	Tdo2<tm1b(KOMP)Mbp>/Tdo2<+>	C57BL/6N-Tdo2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288765	M	MP:0000266	abnormal heart morphology	Tdo2<tm1b(KOMP)Mbp>/Tdo2<+>	C57BL/6N-Tdo2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288765	M	MP:0002833	increased heart weight	Tdo2<tm1b(KOMP)Mbp>/Tdo2<+>	C57BL/6N-Tdo2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288765	F	MP:0001120	abnormal uterus morphology	Tdo2<tm1b(KOMP)Mbp>/Tdo2<+>	C57BL/6N-Tdo2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288765	M	MP:0000274	enlarged heart	Tdo2<tm1b(KOMP)Mbp>/Tdo2<+>	C57BL/6N-Tdo2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288766	F	MP:0001297	microphthalmia	Tdo2<tm1b(KOMP)Mbp>/Tdo2<tm1b(KOMP)Mbp>	C57BL/6N-Tdo2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288766	F	MP:0001697	abnormal embryo size	Tdo2<tm1b(KOMP)Mbp>/Tdo2<tm1b(KOMP)Mbp>	C57BL/6N-Tdo2<tm1b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:6288767	M	MP:0010024	increased total body fat amount	Telo2<em1(IMPC)J>/Telo2<+>	C57BL/6NJ-Telo2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6288768	F	MP:0010123	increased bone mineral content	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288768	M	MP:0000063	decreased bone mineral density	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288768	M	MP:0004953	decreased spleen weight	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288768	F	MP:0001293	anophthalmia	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288768	F	MP:0010053	decreased grip strength	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288768	M	MP:0002834	decreased heart weight	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288768	F	MP:0010025	decreased total body fat amount	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288768	M	MP:0013278	decreased fasting circulating glucose level	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288768	M	MP:0002768	small adrenal glands	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288768	M	MP:0011874	enlarged urinary bladder	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288768	F	MP:0001314	cornea opacity	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288768	F	MP:0010052	increased grip strength	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288768	F	MP:0000157	abnormal sternum morphology	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288768	M	MP:0003961	decreased lean body mass	Tenm4<em1(IMPC)Tcp>/Tenm4<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288769	M	MP:0001925	male infertility	Tg<em1(IMPC)J>/Tg<em1(IMPC)J>	C57BL/6NJ-Tg<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288769	F	MP:0001392	abnormal locomotor behavior	Tg<em1(IMPC)J>/Tg<em1(IMPC)J>	C57BL/6NJ-Tg<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288769	F	MP:0010506	prolonged RR interval	Tg<em1(IMPC)J>/Tg<em1(IMPC)J>	C57BL/6NJ-Tg<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288769	M	MP:0013279	increased fasting circulating glucose level	Tg<em1(IMPC)J>/Tg<em1(IMPC)J>	C57BL/6NJ-Tg<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288769	F	MP:0000367	abnormal coat/ hair morphology	Tg<em1(IMPC)J>/Tg<em1(IMPC)J>	C57BL/6NJ-Tg<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288769	F	MP:0001417	decreased exploration in new environment	Tg<em1(IMPC)J>/Tg<em1(IMPC)J>	C57BL/6NJ-Tg<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288769	F	MP:0001402	decreased locomotor activity	Tg<em1(IMPC)J>/Tg<em1(IMPC)J>	C57BL/6NJ-Tg<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288772	F	MP:0010052	increased grip strength	Thap1<em1(IMPC)J>/Thap1<+>	C57BL/6NJ-Thap1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288772	M	MP:0001312	abnormal cornea morphology	Thap1<em1(IMPC)J>/Thap1<+>	C57BL/6NJ-Thap1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288773	M	MP:0001406	abnormal gait	Th<em1(IMPC)H>/Th<+>	C57BL/6N-Th<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288774	F	MP:0002637	small uterus	Timm13<em1(IMPC)Tcp>/Timm13<+>	C57BL/6NCrl-Timm13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288774	F	MP:0020420	abnormal freezing behavior	Timm13<em1(IMPC)Tcp>/Timm13<+>	C57BL/6NCrl-Timm13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288774	F	MP:0000689	abnormal spleen morphology	Timm13<em1(IMPC)Tcp>/Timm13<+>	C57BL/6NCrl-Timm13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288774	F	MP:0000598	abnormal liver morphology	Timm13<em1(IMPC)Tcp>/Timm13<+>	C57BL/6NCrl-Timm13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288774	M	MP:0003068	enlarged kidney	Timm13<em1(IMPC)Tcp>/Timm13<+>	C57BL/6NCrl-Timm13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288774	M	MP:0002059	abnormal seminal vesicle morphology	Timm13<em1(IMPC)Tcp>/Timm13<+>	C57BL/6NCrl-Timm13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288774	F	MP:0000709	enlarged thymus	Timm13<em1(IMPC)Tcp>/Timm13<+>	C57BL/6NCrl-Timm13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288776	F	MP:0002339	abnormal lymph node morphology	Tle4<em1(IMPC)Mbp>/Tle4<em1(IMPC)Mbp>	C57BL/6NCrl-Tle4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288776	F	MP:0002092	abnormal eye morphology	Tle4<em1(IMPC)Mbp>/Tle4<em1(IMPC)Mbp>	C57BL/6NCrl-Tle4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288776	M	MP:0000492	abnormal rectum morphology	Tle4<em1(IMPC)Mbp>/Tle4<em1(IMPC)Mbp>	C57BL/6NCrl-Tle4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288776	F	MP:0000702	enlarged lymph nodes	Tle4<em1(IMPC)Mbp>/Tle4<em1(IMPC)Mbp>	C57BL/6NCrl-Tle4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288776	M	MP:0000599	enlarged liver	Tle4<em1(IMPC)Mbp>/Tle4<em1(IMPC)Mbp>	C57BL/6NCrl-Tle4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288776	M	MP:0001402	decreased locomotor activity	Tle4<em1(IMPC)Mbp>/Tle4<em1(IMPC)Mbp>	C57BL/6NCrl-Tle4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288776	M	MP:0001925	male infertility	Tle4<em1(IMPC)Mbp>/Tle4<em1(IMPC)Mbp>	C57BL/6NCrl-Tle4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288776	F	MP:0005293	impaired glucose tolerance	Tle4<em1(IMPC)Mbp>/Tle4<em1(IMPC)Mbp>	C57BL/6NCrl-Tle4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288776	F	MP:0002135	abnormal kidney morphology	Tle4<em1(IMPC)Mbp>/Tle4<em1(IMPC)Mbp>	C57BL/6NCrl-Tle4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288776	F	MP:0002989	small kidney	Tle4<em1(IMPC)Mbp>/Tle4<em1(IMPC)Mbp>	C57BL/6NCrl-Tle4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288776	M	MP:0002060	abnormal skin morphology	Tle4<em1(IMPC)Mbp>/Tle4<em1(IMPC)Mbp>	C57BL/6NCrl-Tle4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288778	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Tm2d1<em1(IMPC)Bay>/Tm2d1<+>	C57BL/6N-Tm2d1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288778	F	MP:0002608	increased hematocrit	Tm2d1<em1(IMPC)Bay>/Tm2d1<+>	C57BL/6N-Tm2d1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288780	M	MP:0001489	decreased startle reflex	Tm2d2<em1(IMPC)Bay>/Tm2d2<+>	C57BL/6N-Tm2d2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288786	F	MP:0001469	abnormal contextual conditioning behavior	Tmprss2<tm2b(EUCOMM)Hmgu>/Tmprss2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Tmprss2<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6288786	M	MP:0005140	decreased cardiac muscle contractility	Tmprss2<tm2b(EUCOMM)Hmgu>/Tmprss2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Tmprss2<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6288786	F	MP:0005292	improved glucose tolerance	Tmprss2<tm2b(EUCOMM)Hmgu>/Tmprss2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Tmprss2<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6288786	F	MP:0005568	increased circulating total protein level	Tmprss2<tm2b(EUCOMM)Hmgu>/Tmprss2<tm2b(EUCOMM)Hmgu>	C57BL/6N-Tmprss2<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6288787	F	MP:0002606	increased basophil cell number	Tnip1<tm1b(EUCOMM)Hmgu>/Tnip1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnip1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288787	F	MP:0005560	decreased circulating glucose level	Tnip1<tm1b(EUCOMM)Hmgu>/Tnip1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnip1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288787	F	MP:0020421	increased freezing behavior	Tnip1<tm1b(EUCOMM)Hmgu>/Tnip1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnip1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288787	M	MP:0010506	prolonged RR interval	Tnip1<tm1b(EUCOMM)Hmgu>/Tnip1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnip1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288787	M	MP:0005561	increased mean corpuscular hemoglobin	Tnip1<tm1b(EUCOMM)Hmgu>/Tnip1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnip1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288787	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Tnip1<tm1b(EUCOMM)Hmgu>/Tnip1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnip1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288787	F	MP:0004151	decreased circulating iron level	Tnip1<tm1b(EUCOMM)Hmgu>/Tnip1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnip1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288787	F	MP:0005627	increased circulating potassium level	Tnip1<tm1b(EUCOMM)Hmgu>/Tnip1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnip1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288787	F	MP:0012362	increased large unstained cell number	Tnip1<tm1b(EUCOMM)Hmgu>/Tnip1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnip1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288787	M	MP:0002644	decreased circulating triglyceride level	Tnip1<tm1b(EUCOMM)Hmgu>/Tnip1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnip1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288787	F	MP:0005016	decreased lymphocyte cell number	Tnip1<tm1b(EUCOMM)Hmgu>/Tnip1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnip1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288789	F	MP:0011436	decreased urine magnesium level	Toe1<tm1.1(KOMP)Vlcg>/Toe1<+>	C57BL/6N-Toe1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6288790	M	MP:0000218	increased leukocyte cell number	Tomm20<em1(IMPC)J>/Tomm20<+>	C57BL/6NJ-Tomm20<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288791	M	MP:0010579	increased heart left ventricle size	Tonsl<em1(IMPC)Bay>/Tonsl<+>	C57BL/6N-Tonsl<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288793	M	MP:0000706	small thymus	Top2a<em2(IMPC)Tcp>/Top2a<+>	C57BL/6NCrl-Top2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288793	M	MP:0002060	abnormal skin morphology	Top2a<em2(IMPC)Tcp>/Top2a<+>	C57BL/6NCrl-Top2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288793	M	MP:0000598	abnormal liver morphology	Top2a<em2(IMPC)Tcp>/Top2a<+>	C57BL/6NCrl-Top2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288793	M	MP:0002135	abnormal kidney morphology	Top2a<em2(IMPC)Tcp>/Top2a<+>	C57BL/6NCrl-Top2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288793	M	MP:0000692	small spleen	Top2a<em2(IMPC)Tcp>/Top2a<+>	C57BL/6NCrl-Top2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288793	M	MP:0011874	enlarged urinary bladder	Top2a<em2(IMPC)Tcp>/Top2a<+>	C57BL/6NCrl-Top2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288793	F	MP:0001297	microphthalmia	Top2a<em2(IMPC)Tcp>/Top2a<+>	C57BL/6NCrl-Top2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288793	M	MP:0005343	increased circulating aspartate transaminase level	Top2a<em2(IMPC)Tcp>/Top2a<+>	C57BL/6NCrl-Top2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288793	M	MP:0002059	abnormal seminal vesicle morphology	Top2a<em2(IMPC)Tcp>/Top2a<+>	C57BL/6NCrl-Top2a<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288795	F	MP:0010124	decreased bone mineral content	Trappc2l<em1(IMPC)Mbp>/Trappc2l<em1(IMPC)Mbp>	C57BL/6N-Trappc2l<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288795	M	MP:0000274	enlarged heart	Trappc2l<em1(IMPC)Mbp>/Trappc2l<em1(IMPC)Mbp>	C57BL/6N-Trappc2l<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288795	M	MP:0001925	male infertility	Trappc2l<em1(IMPC)Mbp>/Trappc2l<em1(IMPC)Mbp>	C57BL/6N-Trappc2l<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288795	F	MP:0001258	decreased body length	Trappc2l<em1(IMPC)Mbp>/Trappc2l<em1(IMPC)Mbp>	C57BL/6N-Trappc2l<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288795	M	MP:0001147	small testis	Trappc2l<em1(IMPC)Mbp>/Trappc2l<em1(IMPC)Mbp>	C57BL/6N-Trappc2l<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288795	M	MP:0002875	decreased erythrocyte cell number	Trappc2l<em1(IMPC)Mbp>/Trappc2l<em1(IMPC)Mbp>	C57BL/6N-Trappc2l<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288795	M	MP:0009142	decreased prepulse inhibition	Trappc2l<em1(IMPC)Mbp>/Trappc2l<em1(IMPC)Mbp>	C57BL/6N-Trappc2l<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288795	M	MP:0001146	abnormal testis morphology	Trappc2l<em1(IMPC)Mbp>/Trappc2l<em1(IMPC)Mbp>	C57BL/6N-Trappc2l<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288795	F	MP:0001926	female infertility	Trappc2l<em1(IMPC)Mbp>/Trappc2l<em1(IMPC)Mbp>	C57BL/6N-Trappc2l<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288795	M	MP:0000266	abnormal heart morphology	Trappc2l<em1(IMPC)Mbp>/Trappc2l<em1(IMPC)Mbp>	C57BL/6N-Trappc2l<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288795	F	MP:0020420	abnormal freezing behavior	Trappc2l<em1(IMPC)Mbp>/Trappc2l<em1(IMPC)Mbp>	C57BL/6N-Trappc2l<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288795	M	MP:0002833	increased heart weight	Trappc2l<em1(IMPC)Mbp>/Trappc2l<em1(IMPC)Mbp>	C57BL/6N-Trappc2l<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288795	M	MP:0005561	increased mean corpuscular hemoglobin	Trappc2l<em1(IMPC)Mbp>/Trappc2l<em1(IMPC)Mbp>	C57BL/6N-Trappc2l<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288796	M	MP:0010024	increased total body fat amount	Trf<em1(IMPC)J>/Trf<+>	C57BL/6NJ-Trf<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288796	F	MP:0002590	increased mean corpuscular volume	Trf<em1(IMPC)J>/Trf<+>	C57BL/6NJ-Trf<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288797	F	MP:0011965	decreased total retina thickness	Trib2<tm1b(KOMP)Wtsi>/Trib2<+>	C57BL/6N-Trib2<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288797	F	MP:0003733	abnormal retina inner nuclear layer morphology	Trib2<tm1b(KOMP)Wtsi>/Trib2<+>	C57BL/6N-Trib2<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288798	M	MP:0002941	increased circulating alanine transaminase level	Trim16<em1(IMPC)Tcp>/Trim16<em1(IMPC)Tcp>	C57BL/6NCrl-Trim16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288798	F	MP:0000157	abnormal sternum morphology	Trim16<em1(IMPC)Tcp>/Trim16<em1(IMPC)Tcp>	C57BL/6NCrl-Trim16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288798	M	MP:0002060	abnormal skin morphology	Trim16<em1(IMPC)Tcp>/Trim16<em1(IMPC)Tcp>	C57BL/6NCrl-Trim16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288798	M	MP:0010067	increased red blood cell distribution width	Trim16<em1(IMPC)Tcp>/Trim16<em1(IMPC)Tcp>	C57BL/6NCrl-Trim16<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288801	M	MP:0001891	hydrocephaly	Trip6<tm1b(EUCOMM)Hmgu>/Trip6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trip6<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288801	F	MP:0000438	abnormal cranium morphology	Trip6<tm1b(EUCOMM)Hmgu>/Trip6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trip6<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288801	M	MP:0010378	increased respiratory quotient	Trip6<tm1b(EUCOMM)Hmgu>/Trip6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trip6<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288802	M	MP:0003961	decreased lean body mass	Tsga13<em1(IMPC)J>/Tsga13<em1(IMPC)J>	C57BL/6NJ-Tsga13<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288803	F	MP:0010052	increased grip strength	Tspan9<em1(IMPC)J>/Tspan9<em1(IMPC)J>	C57BL/6NJ-Tspan9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288805	F	MP:0000689	abnormal spleen morphology	Ift70b<em1(IMPC)Bay>/Ift70b<em1(IMPC)Bay>	C57BL/6N-Ift70b<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288806	M	MP:0000367	abnormal coat/ hair morphology	Tubb4b<em1(IMPC)J>/Tubb4b<+>	C57BL/6NJ-Tubb4b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288807	M	MP:0011100	preweaning lethality, complete penetrance	Tulp4<em1(IMPC)Mbp>/Tulp4<em1(IMPC)Mbp>	C57BL/6NCrl-Tulp4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288808	F	MP:0001697	abnormal embryo size	Ubap2l<em1(IMPC)Bay>/Ubap2l<em1(IMPC)Bay>	C57BL/6N-Ubap2l<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288809	F	MP:0002151	abnormal neural tube morphology	Ubc<em1(IMPC)Mbp>/Ubc<em1(IMPC)Mbp>	C57BL/6N-Ubc<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288810	F	MP:0001566	increased circulating phosphate level	Ube2i<em1(IMPC)J>/Ube2i<+>	C57BL/6NJ-Ube2i<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288810	M	MP:0001392	abnormal locomotor behavior	Ube2i<em1(IMPC)J>/Ube2i<+>	C57BL/6NJ-Ube2i<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288810	F	MP:0000218	increased leukocyte cell number	Ube2i<em1(IMPC)J>/Ube2i<+>	C57BL/6NJ-Ube2i<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288811	M	MP:0003743	abnormal facial morphology	Ube3b<em1(IMPC)Bay>/Ube3b<em1(IMPC)Bay>	C57BL/6N-Ube3b<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288812	F	MP:0002966	decreased circulating alkaline phosphatase level	Ubp1<tm1b(KOMP)Mbp>/Ubp1<+>	C57BL/6N-Ubp1<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6288812	M	MP:0005553	increased circulating creatinine level	Ubp1<tm1b(KOMP)Mbp>/Ubp1<+>	C57BL/6N-Ubp1<tm1b(KOMP)Mbp>/Bay	N	MGI:5576271
MGI:6288815	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Uck2<em1(IMPC)J>/Uck2<em1(IMPC)J>	C57BL/6NJ-Uck2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288815	F	MP:0002590	increased mean corpuscular volume	Uck2<em1(IMPC)J>/Uck2<em1(IMPC)J>	C57BL/6NJ-Uck2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288815	M	MP:0002060	abnormal skin morphology	Uck2<em1(IMPC)J>/Uck2<em1(IMPC)J>	C57BL/6NJ-Uck2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288817	F	MP:0008935	decreased mean platelet volume	Uqcrq<tm1b(EUCOMM)Hmgu>/Uqcrq<+>	C57BL/6N-Uqcrq<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6288819	M	MP:0004953	decreased spleen weight	Usp45<em1(IMPC)H>/Usp45<em1(IMPC)H>	C57BL/6NTac-Usp45<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288819	M	MP:0000222	decreased neutrophil cell number	Usp45<em1(IMPC)H>/Usp45<em1(IMPC)H>	C57BL/6NTac-Usp45<em1(IMPC)H>/H	N	MGI:5576271
MGI:6288820	M	MP:0003394	increased cardiac output	Vars2<em1(IMPC)Bay>/Vars2<+>	C57BL/6N-Vars2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288820	F	MP:0011960	abnormal eye anterior chamber depth	Vars2<em1(IMPC)Bay>/Vars2<+>	C57BL/6N-Vars2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288822	M	MP:0001488	increased startle reflex	Vdac1<tm1b(EUCOMM)Wtsi>/Vdac1<+>	C57BL/6N-Vdac1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288823	F	MP:0005333	decreased heart rate	Wbp1l<tm2b(EUCOMM)Hmgu>/Wbp1l<tm2b(EUCOMM)Hmgu>	C57BL/6N-Wbp1l<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288823	F	MP:0010570	prolonged ST segment	Wbp1l<tm2b(EUCOMM)Hmgu>/Wbp1l<tm2b(EUCOMM)Hmgu>	C57BL/6N-Wbp1l<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288823	F	MP:0011239	abnormal skin coloration	Wbp1l<tm2b(EUCOMM)Hmgu>/Wbp1l<tm2b(EUCOMM)Hmgu>	C57BL/6N-Wbp1l<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288823	F	MP:0011960	abnormal eye anterior chamber depth	Wbp1l<tm2b(EUCOMM)Hmgu>/Wbp1l<tm2b(EUCOMM)Hmgu>	C57BL/6N-Wbp1l<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288823	F	MP:0010506	prolonged RR interval	Wbp1l<tm2b(EUCOMM)Hmgu>/Wbp1l<tm2b(EUCOMM)Hmgu>	C57BL/6N-Wbp1l<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288823	F	MP:0001399	hyperactivity	Wbp1l<tm2b(EUCOMM)Hmgu>/Wbp1l<tm2b(EUCOMM)Hmgu>	C57BL/6N-Wbp1l<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288827	M	MP:0001399	hyperactivity	Wdr41<em1(IMPC)J>/Wdr41<em1(IMPC)J>	C57BL/6NJ-Wdr41<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288827	M	MP:0001556	increased circulating HDL cholesterol level	Wdr41<em1(IMPC)J>/Wdr41<em1(IMPC)J>	C57BL/6NJ-Wdr41<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288829	M	MP:0001697	abnormal embryo size	Wdr45b<em1(IMPC)Bay>/Wdr45b<em1(IMPC)Bay>	C57BL/6N-Wdr45b<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288830	M	MP:0000266	abnormal heart morphology	Dync2i1<em1(IMPC)Tcp>/Dync2i1<em1(IMPC)Tcp>	C57BL/6NCrl-Dync2i1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288831	F	MP:0001325	abnormal retina morphology	Wrnip1<tm1b(EUCOMM)Wtsi>/Wrnip1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Wrnip1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288831	M	MP:0002590	increased mean corpuscular volume	Wrnip1<tm1b(EUCOMM)Wtsi>/Wrnip1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Wrnip1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288831	M	MP:0002059	abnormal seminal vesicle morphology	Wrnip1<tm1b(EUCOMM)Wtsi>/Wrnip1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Wrnip1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6288832	F	MP:0003961	decreased lean body mass	Ythdc2<em1(IMPC)Bay>/Ythdc2<em1(IMPC)Bay>	C57BL/6N-Ythdc2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288832	M	MP:0001925	male infertility	Ythdc2<em1(IMPC)Bay>/Ythdc2<em1(IMPC)Bay>	C57BL/6N-Ythdc2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288832	F	MP:0001926	female infertility	Ythdc2<em1(IMPC)Bay>/Ythdc2<em1(IMPC)Bay>	C57BL/6N-Ythdc2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288832	F	MP:0000063	decreased bone mineral density	Ythdc2<em1(IMPC)Bay>/Ythdc2<em1(IMPC)Bay>	C57BL/6N-Ythdc2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288832	F	MP:0010124	decreased bone mineral content	Ythdc2<em1(IMPC)Bay>/Ythdc2<em1(IMPC)Bay>	C57BL/6N-Ythdc2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288832	F	MP:0002834	decreased heart weight	Ythdc2<em1(IMPC)Bay>/Ythdc2<em1(IMPC)Bay>	C57BL/6N-Ythdc2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288833	M	MP:0005287	narrow eye opening	Zbtb5<tm2b(EUCOMM)Hmgu>/Zbtb5<tm2b(EUCOMM)Hmgu>	C57BL/6N-Zbtb5<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288833	M	MP:0004924	abnormal behavior	Zbtb5<tm2b(EUCOMM)Hmgu>/Zbtb5<tm2b(EUCOMM)Hmgu>	C57BL/6N-Zbtb5<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288833	F	MP:0003731	abnormal retina outer nuclear layer morphology	Zbtb5<tm2b(EUCOMM)Hmgu>/Zbtb5<tm2b(EUCOMM)Hmgu>	C57BL/6N-Zbtb5<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288833	M	MP:0001402	decreased locomotor activity	Zbtb5<tm2b(EUCOMM)Hmgu>/Zbtb5<tm2b(EUCOMM)Hmgu>	C57BL/6N-Zbtb5<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288833	M	MP:0001488	increased startle reflex	Zbtb5<tm2b(EUCOMM)Hmgu>/Zbtb5<tm2b(EUCOMM)Hmgu>	C57BL/6N-Zbtb5<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288833	M	MP:0001293	anophthalmia	Zbtb5<tm2b(EUCOMM)Hmgu>/Zbtb5<tm2b(EUCOMM)Hmgu>	C57BL/6N-Zbtb5<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288833	F	MP:0003733	abnormal retina inner nuclear layer morphology	Zbtb5<tm2b(EUCOMM)Hmgu>/Zbtb5<tm2b(EUCOMM)Hmgu>	C57BL/6N-Zbtb5<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288833	M	MP:0020870	decreased thigmotaxis	Zbtb5<tm2b(EUCOMM)Hmgu>/Zbtb5<tm2b(EUCOMM)Hmgu>	C57BL/6N-Zbtb5<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288834	F	MP:0000219	increased neutrophil cell number	Zc3h12c<em1(IMPC)Tcp>/Zc3h12c<em1(IMPC)Tcp>	C57BL/6NCrl-Zc3h12c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288834	F	MP:0010124	decreased bone mineral content	Zc3h12c<em1(IMPC)Tcp>/Zc3h12c<em1(IMPC)Tcp>	C57BL/6NCrl-Zc3h12c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288834	M	MP:0000063	decreased bone mineral density	Zc3h12c<em1(IMPC)Tcp>/Zc3h12c<em1(IMPC)Tcp>	C57BL/6NCrl-Zc3h12c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288834	F	MP:0010052	increased grip strength	Zc3h12c<em1(IMPC)Tcp>/Zc3h12c<em1(IMPC)Tcp>	C57BL/6NCrl-Zc3h12c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288834	F	MP:0005016	decreased lymphocyte cell number	Zc3h12c<em1(IMPC)Tcp>/Zc3h12c<em1(IMPC)Tcp>	C57BL/6NCrl-Zc3h12c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288834	M	MP:0001552	increased circulating triglyceride level	Zc3h12c<em1(IMPC)Tcp>/Zc3h12c<em1(IMPC)Tcp>	C57BL/6NCrl-Zc3h12c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6288837	M	MP:0001510	abnormal coat appearance	Zfp395<tm1b(EUCOMM)Wtsi>/Zfp395<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp395<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288837	M	MP:0011239	abnormal skin coloration	Zfp395<tm1b(EUCOMM)Wtsi>/Zfp395<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp395<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288837	F	MP:0003733	abnormal retina inner nuclear layer morphology	Zfp395<tm1b(EUCOMM)Wtsi>/Zfp395<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp395<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288838	F	MP:0000689	abnormal spleen morphology	Zfp488<em1(IMPC)Bay>/Zfp488<em1(IMPC)Bay>	C57BL/6N-Zfp488<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6288839	M	MP:0000433	microcephaly	Zfp503<em1(IMPC)Mbp>/Zfp503<em1(IMPC)Mbp>	C57BL/6N-Zfp503<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288839	M	MP:0001697	abnormal embryo size	Zfp503<em1(IMPC)Mbp>/Zfp503<em1(IMPC)Mbp>	C57BL/6N-Zfp503<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6288840	M	MP:0004931	enlarged epididymis	Zfp558<em1(IMPC)Mbp>/Zfp558<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp558<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288840	M	MP:0005419	decreased circulating serum albumin level	Zfp558<em1(IMPC)Mbp>/Zfp558<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp558<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288840	M	MP:0005560	decreased circulating glucose level	Zfp558<em1(IMPC)Mbp>/Zfp558<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp558<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288840	M	MP:0002631	abnormal epididymis morphology	Zfp558<em1(IMPC)Mbp>/Zfp558<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp558<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288840	M	MP:0005554	decreased circulating creatinine level	Zfp558<em1(IMPC)Mbp>/Zfp558<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp558<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288840	M	MP:0005567	decreased circulating total protein level	Zfp558<em1(IMPC)Mbp>/Zfp558<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp558<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6288841	F	MP:0004222	iris synechia	Zfp597<em1(IMPC)J>/Zfp597<em1(IMPC)J>	C57BL/6NJ-Zfp597<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288842	M	MP:0009142	decreased prepulse inhibition	Zfp609<tm1b(EUCOMM)Hmgu>/Zfp609<+>	C57BL/6N-Zfp609<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288842	M	MP:0011239	abnormal skin coloration	Zfp609<tm1b(EUCOMM)Hmgu>/Zfp609<+>	C57BL/6N-Zfp609<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288843	M	MP:0001406	abnormal gait	Zfp830<tm1b(EUCOMM)Hmgu>/Zfp830<+>	C57BL/6N-Zfp830<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288843	F	MP:0001325	abnormal retina morphology	Zfp830<tm1b(EUCOMM)Hmgu>/Zfp830<+>	C57BL/6N-Zfp830<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6288844	M	MP:0002764	short tibia	Zfp831<tm1b(KOMP)Wtsi>/Zfp831<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp831<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288844	M	MP:0001510	abnormal coat appearance	Zfp831<tm1b(KOMP)Wtsi>/Zfp831<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp831<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6288845	M	MP:0000745	tremors	Zfpl1<tm2b(EUCOMM)Wtsi>/Zfpl1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Zfpl1<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288847	M	MP:0010379	decreased respiratory quotient	Zscan21<tm2b(EUCOMM)Wtsi>/Zscan21<+>	C57BL/6N-Zscan21<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288847	M	MP:0011239	abnormal skin coloration	Zscan21<tm2b(EUCOMM)Wtsi>/Zscan21<+>	C57BL/6N-Zscan21<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288847	M	MP:0011965	decreased total retina thickness	Zscan21<tm2b(EUCOMM)Wtsi>/Zscan21<+>	C57BL/6N-Zscan21<tm2b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6288848	F	MP:0001406	abnormal gait	Zscan5b<em1(IMPC)J>/Zscan5b<em1(IMPC)J>	C57BL/6NJ-Zscan5b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6288848	F	MP:0001304	cataract	Zscan5b<em1(IMPC)J>/Zscan5b<em1(IMPC)J>	C57BL/6NJ-Zscan5b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6294052	M	MP:0020395	abnormal response to social novelty	Pak2<Gt(OST104058)Lex>/Pak2<+>	B6;129S5-Pak2<Gt(OST104058)Lex>/J	N	30134165
MGI:6294052	M	MP:0001409	increased stereotypic behavior	Pak2<Gt(OST104058)Lex>/Pak2<+>	B6;129S5-Pak2<Gt(OST104058)Lex>/J	N	30134165
MGI:6294052	M	MP:0020508	decreased dendritic spine density	Pak2<Gt(OST104058)Lex>/Pak2<+>	B6;129S5-Pak2<Gt(OST104058)Lex>/J	N	30134165
MGI:6294052	M	MP:0001441	increased grooming behavior	Pak2<Gt(OST104058)Lex>/Pak2<+>	B6;129S5-Pak2<Gt(OST104058)Lex>/J	N	30134165
MGI:6294052	M	MP:0020849	abnormal actin cytoskeleton morphology	Pak2<Gt(OST104058)Lex>/Pak2<+>	B6;129S5-Pak2<Gt(OST104058)Lex>/J	N	30134165
MGI:6294052	M	MP:0002912	abnormal excitatory postsynaptic potential	Pak2<Gt(OST104058)Lex>/Pak2<+>	B6;129S5-Pak2<Gt(OST104058)Lex>/J	N	30134165
MGI:6294052	M	MP:0001360	abnormal social investigation	Pak2<Gt(OST104058)Lex>/Pak2<+>	B6;129S5-Pak2<Gt(OST104058)Lex>/J	N	30134165
MGI:6294052	M	MP:0005386	behavior/neurological phenotype	Pak2<Gt(OST104058)Lex>/Pak2<+>	B6;129S5-Pak2<Gt(OST104058)Lex>/J	Y	30134165
MGI:6294052	M	MP:0020551	abnormal postsynaptic density morphology	Pak2<Gt(OST104058)Lex>/Pak2<+>	B6;129S5-Pak2<Gt(OST104058)Lex>/J	N	30134165
MGI:6294052	M	MP:0006009	abnormal neuronal migration	Pak2<Gt(OST104058)Lex>/Pak2<+>	B6;129S5-Pak2<Gt(OST104058)Lex>/J	N	30134165
MGI:6294052	M	MP:0001473	reduced long-term potentiation	Pak2<Gt(OST104058)Lex>/Pak2<+>	B6;129S5-Pak2<Gt(OST104058)Lex>/J	N	30134165
MGI:6294052	M	MP:0001361	social withdrawal	Pak2<Gt(OST104058)Lex>/Pak2<+>	B6;129S5-Pak2<Gt(OST104058)Lex>/J	N	30134165
MGI:6294717	F	MP:0001783	decreased white adipose tissue amount	Igf2bp2<tm1Mini>/Igf2bp2<tm1Mini>	B6.129P2-Igf2bp2<tm1Mini>	N	25863250
MGI:6294717	M	MP:0008844	decreased subcutaneous adipose tissue amount	Igf2bp2<tm1Mini>/Igf2bp2<tm1Mini>	B6.129P2-Igf2bp2<tm1Mini>	N	25863250
MGI:6294717	F	MP:0002981	increased liver weight	Igf2bp2<tm1Mini>/Igf2bp2<tm1Mini>	B6.129P2-Igf2bp2<tm1Mini>	N	25863250
MGI:6294717	M	MP:0001258	decreased body length	Igf2bp2<tm1Mini>/Igf2bp2<tm1Mini>	B6.129P2-Igf2bp2<tm1Mini>	N	25863250
MGI:6295127	M	MP:0001262	decreased body weight	Phf6<em1Azbi>/Y	B6.Cg-Phf6<em1Azbi>	N	30403997
MGI:6295127	M	MP:0002906	increased susceptibility to pharmacologically induced seizures	Phf6<em1Azbi>/Y	B6.Cg-Phf6<em1Azbi>	N	30403997
MGI:6295127	M	MP:0002757	decreased vertical activity	Phf6<em1Azbi>/Y	B6.Cg-Phf6<em1Azbi>	N	30403997
MGI:6295127	M	MP:0004811	abnormal neuron physiology	Phf6<em1Azbi>/Y	B6.Cg-Phf6<em1Azbi>	N	30403997
MGI:6295127	M	MP:0001458	abnormal object recognition memory	Phf6<em1Azbi>/Y	B6.Cg-Phf6<em1Azbi>	N	30403997
MGI:6295127	M	MP:0001258	decreased body length	Phf6<em1Azbi>/Y	B6.Cg-Phf6<em1Azbi>	N	30403997
MGI:6295127	M	MP:0001489	decreased startle reflex	Phf6<em1Azbi>/Y	B6.Cg-Phf6<em1Azbi>	N	30403997
MGI:6295127	M	MP:0003468	increased single cell response intensity	Phf6<em1Azbi>/Y	B6.Cg-Phf6<em1Azbi>	N	30403997
MGI:6295127	M	MP:0003466	decreased single cell response threshold	Phf6<em1Azbi>/Y	B6.Cg-Phf6<em1Azbi>	N	30403997
MGI:6295127	M	MP:0005402	abnormal action potential	Phf6<em1Azbi>/Y	B6.Cg-Phf6<em1Azbi>	N	30403997
MGI:6295127	M	MP:0009454	impaired contextual conditioning behavior	Phf6<em1Azbi>/Y	B6.Cg-Phf6<em1Azbi>	N	30403997
MGI:6295127	M	MP:0020396	abnormal social recognition	Phf6<em1Azbi>/Y	B6.Cg-Phf6<em1Azbi>	N	30403997
MGI:6295127	M	MP:0001417	decreased exploration in new environment	Phf6<em1Azbi>/Y	B6.Cg-Phf6<em1Azbi>	N	30403997
MGI:6295150	M	MP:0011089	perinatal lethality, complete penetrance	Phf6<em2Azbi>/Y	involves: C57BL/6 * CBA	N	30403997
MGI:6295153	F	MP:0011089	perinatal lethality, complete penetrance	Phf6<em2Azbi>/Phf6<em2Azbi>	involves: C57BL/6 * CBA	N	30403997
MGI:6295357	M	MP:0001406	abnormal gait	Gnao1<em1Rneu>/Gnao1<+>	involves: C57BL/6J * C57BL/6NCrl	N	30682176
MGI:6295357	M	MP:0001405	impaired coordination	Gnao1<em1Rneu>/Gnao1<+>	involves: C57BL/6J * C57BL/6NCrl	N	30682176
MGI:6295357	M	MP:0020424	increased kindling response	Gnao1<em1Rneu>/Gnao1<+>	involves: C57BL/6J * C57BL/6NCrl	N	30682176
MGI:6295357	M	MP:0001407	short stride length	Gnao1<em1Rneu>/Gnao1<+>	involves: C57BL/6J * C57BL/6NCrl	N	30682176
MGI:6295359	F	MP:0010053	decreased grip strength	Gnao1<tm2Rneu>/Gnao1<+>	B6.129S1-Gnao1<tm2Rneu>	N	30682176
MGI:6295359	F	MP:0001405	impaired coordination	Gnao1<tm2Rneu>/Gnao1<+>	B6.129S1-Gnao1<tm2Rneu>	N	30682176
MGI:6295359	F	MP:0001407	short stride length	Gnao1<tm2Rneu>/Gnao1<+>	B6.129S1-Gnao1<tm2Rneu>	N	30682176
MGI:6295477	F	MP:0001262	decreased body weight	Eif3e<tm1Fshb>/Eif3e<+>	C57BL/6N-Eif3e<tm1Fshb>	N	30087825
MGI:6295503	F	MP:0004514	dystocia	Setd3<tm1.1(NCOM)Mfgc>/Setd3<tm1.1(NCOM)Mfgc>	C57BL/6N-Setd3<tm1.1(NCOM)Mfgc>/Tcp	N	30626964
MGI:6295503	F	MP:0001935	decreased litter size	Setd3<tm1.1(NCOM)Mfgc>/Setd3<tm1.1(NCOM)Mfgc>	C57BL/6N-Setd3<tm1.1(NCOM)Mfgc>/Tcp	N	30626964
MGI:6296605	F	MP:0013716	hypolactation	Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296605	F	MP:0002006	neoplasm	Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	Y	21282721
MGI:6296606	F	MP:0010249	lactation failure	Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296606	F	MP:0009505	abnormal mammary gland lobule morphology	Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296606	F	MP:0006269	abnormal mammary gland growth during pregnancy	Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296606	F	MP:0001272	increased metastatic potential	Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296606	F	MP:0009503	abnormal mammary gland duct morphology	Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296606	F	MP:0010299	increased mammary gland tumor incidence	Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296607	F	MP:0001883	increased mammary adenocarcinoma incidence	Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296607	F	MP:0010299	increased mammary gland tumor incidence	Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296608	F	MP:0001883	increased mammary adenocarcinoma incidence	Cdh1<tm1Jjon>/Cdh1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296608	F	MP:0010299	increased mammary gland tumor incidence	Cdh1<tm1Jjon>/Cdh1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296609	F	MP:0013716	hypolactation	Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<+>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296609	F	MP:0001272	increased metastatic potential	Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<+>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296609	F	MP:0010299	increased mammary gland tumor incidence	Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<+>,Tg(Wap-cre)51Nki/0	involves: 129P2/OlaHsd * FVB/N	N	21282721
MGI:6296611	F	MP:0002169	no abnormal phenotype detected	Cdr1os<em2Dpbl>/Cdr1os<em2Dpbl>	C57BL/6J-Cdr1os<em2Dpbl>	N	29887379
MGI:6296612	M	MP:0002169	no abnormal phenotype detected	Cdr1os<em2Dpbl>/Y	C57BL/6J-Cdr1os<em2Dpbl>	N	29887379
MGI:6296614	F	MP:0002169	no abnormal phenotype detected	Cdr1os<em1Dpbl>/Cdr1os<em1Dpbl>	C57BL/6J-Cdr1os<em1Dpbl>	N	29887379
MGI:6296615	M	MP:0002169	no abnormal phenotype detected	Cdr1os<em1Dpbl>/Y	C57BL/6J-Cdr1os<em1Dpbl>	N	29887379
MGI:6297005	M	MP:0013630	increased bone trabecular spacing	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	27732085
MGI:6297005	M	MP:0013304	osteophytes	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	27732085
MGI:6297005	M	MP:0010869	decreased bone trabecula number	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	27732085
MGI:6297005	M	MP:0009346	decreased trabecular bone thickness	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	27732085
MGI:6297005	M	MP:0020137	decreased bone mineralization	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0003560	osteoarthritis	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	27732085
MGI:6297005	M	MP:0006433	abnormal articular cartilage morphology	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	27732085
MGI:6297005	M	MP:0003109	short femur	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0030837	abnormal knee joint morphology	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	27732085
MGI:6297005	M	MP:0004686	decreased length of long bones	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0000130	abnormal trabecular bone morphology	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0009346	decreased trabecular bone thickness	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0010124	decreased bone mineral content	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0005416	abnormal circulating protein level	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0020040	decreased bone ossification	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0013630	increased bone trabecular spacing	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0004984	increased osteoclast cell number	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0004992	increased bone resorption	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0010869	decreased bone trabecula number	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0002904	increased circulating parathyroid hormone level	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0002901	increased urine phosphate level	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0000198	decreased circulating phosphate level	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0000131	abnormal long bone epiphysis morphology	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	27732085
MGI:6297005	M	MP:0010876	decreased bone volume	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0001262	decreased body weight	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0009445	osteomalacia	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0004016	decreased bone mass	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0021190	decreased bone mineral density of lumbar vertebrae	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297005	M	MP:0003055	abnormal long bone epiphyseal plate morphology	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh	involves: FVB/N	N	19933269
MGI:6297092	M	MP:0005560	decreased circulating glucose level	Mlxipl<tm1Kuy>/Mlxipl<tm1Kuy>	B6.129S6-Mlxipl<tm1Kuy>/J	N	29669261
MGI:6297092	F	MP:0005559	increased circulating glucose level	Mlxipl<tm1Kuy>/Mlxipl<tm1Kuy>	B6.129S6-Mlxipl<tm1Kuy>/J	N	29669261
MGI:6302764	M	MP:0001922	reduced male fertility	Borcs7<Q87X>/Borcs7<Q87X>	involves: 129S6/SvEvTac * C57BL/6 * DBA/2	N	30067980
MGI:6303631	F	MP:0009504	abnormal mammary gland epithelium morphology	Atp6v0a2<tm1Kdb>/Atp6v0a2<tm1Kdb>,Tg(MMTV-cre)4Mam/0	involves: 129 * C57BL/6 * FVB	N	27809299
MGI:6303631	F	MP:0013782	abnormal mammary duct terminal end bud morphology	Atp6v0a2<tm1Kdb>/Atp6v0a2<tm1Kdb>,Tg(MMTV-cre)4Mam/0	involves: 129 * C57BL/6 * FVB	N	27809299
MGI:6303631	F	MP:0000662	abnormal branching of the mammary ductal tree	Atp6v0a2<tm1Kdb>/Atp6v0a2<tm1Kdb>,Tg(MMTV-cre)4Mam/0	involves: 129 * C57BL/6 * FVB	N	27809299
MGI:6303631	F	MP:0001882	abnormal lactation	Atp6v0a2<tm1Kdb>/Atp6v0a2<tm1Kdb>,Tg(MMTV-cre)4Mam/0	involves: 129 * C57BL/6 * FVB	N	27809299
MGI:6303631	F	MP:0000628	abnormal mammary gland development	Atp6v0a2<tm1Kdb>/Atp6v0a2<tm1Kdb>,Tg(MMTV-cre)4Mam/0	involves: 129 * C57BL/6 * FVB	N	27809299
MGI:6303631	F	MP:0009503	abnormal mammary gland duct morphology	Atp6v0a2<tm1Kdb>/Atp6v0a2<tm1Kdb>,Tg(MMTV-cre)4Mam/0	involves: 129 * C57BL/6 * FVB	N	27809299
MGI:6303631	F	MP:0012075	impaired mammary gland growth during pregnancy	Atp6v0a2<tm1Kdb>/Atp6v0a2<tm1Kdb>,Tg(MMTV-cre)4Mam/0	involves: 129 * C57BL/6 * FVB	N	27809299
MGI:6303984	F	MP:0005332	abnormal amino acid level	Piga<tm1Tak>/Piga<tm1Tak>,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	15304084
MGI:6303984	F	MP:0002796	impaired skin barrier function	Piga<tm1Tak>/Piga<tm1Tak>,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	15304084
MGI:6303984	F	MP:0001429	dehydration	Piga<tm1Tak>/Piga<tm1Tak>,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	15304084
MGI:6303984	F	MP:0001240	abnormal epidermis stratum corneum morphology	Piga<tm1Tak>/Piga<tm1Tak>,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	15304084
MGI:6303984	F	MP:0009608	abnormal epidermal lamellar body morphology	Piga<tm1Tak>/Piga<tm1Tak>,Tg(KRT5-cre)1Tak/0	involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	N	15304084
MGI:6304006	F	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	Piga<tm1Tak>/Piga<tm1Tak>,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA/Ca	N	19679885
MGI:6304006	F	MP:0002444	abnormal T cell physiology	Piga<tm1Tak>/Piga<tm1Tak>,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA/Ca	N	19679885
MGI:6304006	F	MP:0001828	abnormal T cell activation	Piga<tm1Tak>/Piga<tm1Tak>,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA/Ca	N	19679885
MGI:6304006	F	MP:0008037	abnormal T cell morphology	Piga<tm1Tak>/Piga<tm1Tak>,Tg(FES-cre)31Bsl/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA/Ca	N	19679885
MGI:6304487	F	MP:0011925	abnormal heart echocardiography feature	Tnnc1<tm1.1Jrpi>/Tnnc1<tm1.1Jrpi>	involves: 129S6/SvEvTac * C57BL/6	N	28235781
MGI:6304487	F	MP:0000639	abnormal adrenal gland morphology	Tnnc1<tm1.1Jrpi>/Tnnc1<tm1.1Jrpi>	involves: 129S6/SvEvTac * C57BL/6	N	28235781
MGI:6304487	F	MP:0002573	behavioral despair	Tnnc1<tm1.1Jrpi>/Tnnc1<tm1.1Jrpi>	involves: 129S6/SvEvTac * C57BL/6	N	28235781
MGI:6304487	F	MP:0005333	decreased heart rate	Tnnc1<tm1.1Jrpi>/Tnnc1<tm1.1Jrpi>	involves: 129S6/SvEvTac * C57BL/6	N	28235781
MGI:6304487	F	MP:0002972	abnormal cardiac muscle contractility	Tnnc1<tm1.1Jrpi>/Tnnc1<tm1.1Jrpi>	involves: 129S6/SvEvTac * C57BL/6	N	28235781
MGI:6304487	F	MP:0000783	abnormal forebrain morphology	Tnnc1<tm1.1Jrpi>/Tnnc1<tm1.1Jrpi>	involves: 129S6/SvEvTac * C57BL/6	N	28235781
MGI:6304487	F	MP:0001363	increased anxiety-related response	Tnnc1<tm1.1Jrpi>/Tnnc1<tm1.1Jrpi>	involves: 129S6/SvEvTac * C57BL/6	N	28235781
MGI:6304487	F	MP:0004084	abnormal cardiac muscle relaxation	Tnnc1<tm1.1Jrpi>/Tnnc1<tm1.1Jrpi>	involves: 129S6/SvEvTac * C57BL/6	N	28235781
MGI:6304487	F	MP:0004183	abnormal sympathetic nervous system physiology	Tnnc1<tm1.1Jrpi>/Tnnc1<tm1.1Jrpi>	involves: 129S6/SvEvTac * C57BL/6	N	28235781
MGI:6305794	F	MP:0003313	abnormal locomotor activation	Spata13<em1(IMPC)H>/Spata13<em1(IMPC)H>	C57BL/6NTac-Spata13<em1(IMPC)H>/H	N	31020388
MGI:6307746	F	MP:0030484	abnormal osteocyte lacuna morphology	Fndc5<tm1.1Brsp>/Fndc5<tm1.1Brsp>	involves: C57BL/6J	N	30550785
MGI:6307746	M	MP:0005390	skeleton phenotype	Fndc5<tm1.1Brsp>/Fndc5<tm1.1Brsp>	involves: C57BL/6J	Y	30550785
MGI:6307746	F	MP:0008753	abnormal osteocyte morphology	Fndc5<tm1.1Brsp>/Fndc5<tm1.1Brsp>	involves: C57BL/6J	N	30550785
MGI:6307746	F	MP:0012072	decreased susceptibility to osteoporosis	Fndc5<tm1.1Brsp>/Fndc5<tm1.1Brsp>	involves: C57BL/6J	N	30550785
MGI:6307746	F	MP:0004993	decreased bone resorption	Fndc5<tm1.1Brsp>/Fndc5<tm1.1Brsp>	involves: C57BL/6J	N	30550785
MGI:6307824	M	MP:0005343	increased circulating aspartate transaminase level	H1f8<tm1b(KOMP)Wtsi>/H1f8<tm1b(KOMP)Wtsi>	C57BL/6N-H1f8<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6307824	M	MP:0002941	increased circulating alanine transaminase level	H1f8<tm1b(KOMP)Wtsi>/H1f8<tm1b(KOMP)Wtsi>	C57BL/6N-H1f8<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6307824	M	MP:0005292	improved glucose tolerance	H1f8<tm1b(KOMP)Wtsi>/H1f8<tm1b(KOMP)Wtsi>	C57BL/6N-H1f8<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6314222	M	MP:0002272	abnormal nervous system electrophysiology	Atp1a2<tm1.1Tmklh>/Atp1a2<+>	B6.129S1(Cg)-Atp1a2<tm1.1Tmklh>	N	26911348
MGI:6314222	F	MP:0001405	impaired coordination	Atp1a2<tm1.1Tmklh>/Atp1a2<+>	B6.129S1(Cg)-Atp1a2<tm1.1Tmklh>	N	26911348
MGI:6314222	F	MP:0002572	abnormal emotion/affect behavior	Atp1a2<tm1.1Tmklh>/Atp1a2<+>	B6.129S1(Cg)-Atp1a2<tm1.1Tmklh>	N	26911348
MGI:6314222	F	MP:0001402	decreased locomotor activity	Atp1a2<tm1.1Tmklh>/Atp1a2<+>	B6.129S1(Cg)-Atp1a2<tm1.1Tmklh>	N	26911348
MGI:6314222	M	MP:0001260	increased body weight	Atp1a2<tm1.1Tmklh>/Atp1a2<+>	B6.129S1(Cg)-Atp1a2<tm1.1Tmklh>	N	26911348
MGI:6314222	F	MP:0001441	increased grooming behavior	Atp1a2<tm1.1Tmklh>/Atp1a2<+>	B6.129S1(Cg)-Atp1a2<tm1.1Tmklh>	N	26911348
MGI:6314222	F	MP:0010698	abnormal impulsive behavior control	Atp1a2<tm1.1Tmklh>/Atp1a2<+>	B6.129S1(Cg)-Atp1a2<tm1.1Tmklh>	N	26911348
MGI:6314222	F	MP:0030736	increased glutamic acid level	Atp1a2<tm1.1Tmklh>/Atp1a2<+>	B6.129S1(Cg)-Atp1a2<tm1.1Tmklh>	N	26911348
MGI:6314311	F	MP:0010964	increased compact bone volume	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	M	MP:0003109	short femur	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	M	MP:0009347	increased trabecular bone thickness	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	F	MP:0004148	increased compact bone thickness	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	M	MP:0001262	decreased body weight	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	F	MP:0001399	hyperactivity	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	F	MP:0010379	decreased respiratory quotient	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	M	MP:0005658	increased susceptibility to diet-induced obesity	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	F	MP:0001402	decreased locomotor activity	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	F	MP:0004889	increased energy expenditure	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	F	MP:0009305	decreased retroperitoneal fat pad weight	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	F	MP:0009299	decreased mesenteric fat pad weight	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	F	MP:0009293	decreased inguinal fat pad weight	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	M	MP:0010868	increased bone trabecula number	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	F	MP:0002079	increased circulating insulin level	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	M	MP:0010872	increased trabecular bone mass	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314311	F	MP:0001783	decreased white adipose tissue amount	Npffr2<tm1.1Hhzg>/Npffr2<tm1.1Hhzg>	involves: C57BL/6	N	30413707
MGI:6314318	M	MP:0009238	coiled sperm flagellum	H2ab1<em1Ttas> H2ab2<em1Ttas> H2ab3<em1Ttas>/Y	FVB/NJArc-H2ab2<em1Ttas> H2ab1<em1Ttas> H2ab3<em1Ttas>	N	30704500
MGI:6314318	M	MP:0009237	kinked sperm flagellum	H2ab1<em1Ttas> H2ab2<em1Ttas> H2ab3<em1Ttas>/Y	FVB/NJArc-H2ab2<em1Ttas> H2ab1<em1Ttas> H2ab3<em1Ttas>	N	30704500
MGI:6314318	M	MP:0002216	abnormal seminiferous tubule morphology	H2ab1<em1Ttas> H2ab2<em1Ttas> H2ab3<em1Ttas>/Y	FVB/NJArc-H2ab2<em1Ttas> H2ab1<em1Ttas> H2ab3<em1Ttas>	N	30704500
MGI:6314318	M	MP:0005578	teratozoospermia	H2ab1<em1Ttas> H2ab2<em1Ttas> H2ab3<em1Ttas>/Y	FVB/NJArc-H2ab2<em1Ttas> H2ab1<em1Ttas> H2ab3<em1Ttas>	N	30704500
MGI:6314318	M	MP:0001922	reduced male fertility	H2ab1<em1Ttas> H2ab2<em1Ttas> H2ab3<em1Ttas>/Y	FVB/NJArc-H2ab2<em1Ttas> H2ab1<em1Ttas> H2ab3<em1Ttas>	N	30704500
MGI:6314318	M	MP:0002687	oligozoospermia	H2ab1<em1Ttas> H2ab2<em1Ttas> H2ab3<em1Ttas>/Y	FVB/NJArc-H2ab2<em1Ttas> H2ab1<em1Ttas> H2ab3<em1Ttas>	N	30704500
MGI:6314318	M	MP:0001935	decreased litter size	H2ab1<em1Ttas> H2ab2<em1Ttas> H2ab3<em1Ttas>/Y	FVB/NJArc-H2ab2<em1Ttas> H2ab1<em1Ttas> H2ab3<em1Ttas>	N	30704500
MGI:6314744	F	MP:0001125	abnormal oocyte morphology	Nlrp2<tm1a(KOMP)Wtsi>/Nlrp2<tm1a(KOMP)Wtsi>	Not Specified	N	28317850
MGI:6314744	F	MP:0005389	reproductive system phenotype	Nlrp2<tm1a(KOMP)Wtsi>/Nlrp2<tm1a(KOMP)Wtsi>	Not Specified	Y	28317850
MGI:6314744	F	MP:0031239	increased atretic ovarian follicle number	Nlrp2<tm1a(KOMP)Wtsi>/Nlrp2<tm1a(KOMP)Wtsi>	Not Specified	N	28317850
MGI:6314744	F	MP:0009647	decreased fertilization frequency	Nlrp2<tm1a(KOMP)Wtsi>/Nlrp2<tm1a(KOMP)Wtsi>	Not Specified	N	28317850
MGI:6314744	F	MP:0031381	decreased secondary ovarian follicle number	Nlrp2<tm1a(KOMP)Wtsi>/Nlrp2<tm1a(KOMP)Wtsi>	Not Specified	N	28317850
MGI:6314744	F	MP:0008868	abnormal granulosa cell morphology	Nlrp2<tm1a(KOMP)Wtsi>/Nlrp2<tm1a(KOMP)Wtsi>	Not Specified	N	28317850
MGI:6314744	F	MP:0003718	maternal effect	Nlrp2<tm1a(KOMP)Wtsi>/Nlrp2<tm1a(KOMP)Wtsi>	Not Specified	N	28317850
MGI:6314744	F	MP:0001131	abnormal ovarian follicle morphology	Nlrp2<tm1a(KOMP)Wtsi>/Nlrp2<tm1a(KOMP)Wtsi>	Not Specified	N	28317850
MGI:6315260	F	MP:0002626	increased heart rate	Calm1<em1Gkim>/Calm1<em1Gkim>	C57BL/6N-Calm1<em1Gkim>	N	30322141
MGI:6315471	M	MP:0001925	male infertility	Aktip<tm1a(EUCOMM)Hmgu>/Aktip<tm1a(EUCOMM)Hmgu>	C57BL/6N-Aktip<tm1a(EUCOMM)Hmgu>	N	29635765
MGI:6315559	M	MP:0021118	abnormal paternal behavior	Vmn2r65<tm1.1Dlc>/Vmn2r65<tm1.1Dlc>	B6.Cg-Vmn2r65<tm1.1Dlc>	N	30550786
MGI:6315559	M	MP:0005386	behavior/neurological phenotype	Vmn2r65<tm1.1Dlc>/Vmn2r65<tm1.1Dlc>	B6.Cg-Vmn2r65<tm1.1Dlc>	Y	30550786
MGI:6315559	M	MP:0003863	decreased aggression towards mice	Vmn2r65<tm1.1Dlc>/Vmn2r65<tm1.1Dlc>	B6.Cg-Vmn2r65<tm1.1Dlc>	N	30550786
MGI:6315560	M	MP:0005386	behavior/neurological phenotype	Vmn2r88<tm1.1Dlc>/Vmn2r88<tm1.1Dlc>	B6.Cg-Vmn2r88<tm1.1Dlc>	Y	30550786
MGI:6315561	M	MP:0003863	decreased aggression towards mice	Vmn2r65<tm1.1Dlc>/Vmn2r65<tm1.1Dlc>,Vmn2r88<tm1.1Dlc>/Vmn2r88<tm1.1Dlc>	B6.Cg-Vmn2r65<tm1.1Dlc> Vmn2r88<tm1.1Dlc>	N	30550786
MGI:6315636	M	MP:0001489	decreased startle reflex	Zdhhc9<tm1Lex>/Y	B6.129S5-Zdhhc9<tm1Lex>	N	29944857
MGI:6315636	M	MP:0001262	decreased body weight	Zdhhc9<tm1Lex>/Y	B6.129S5-Zdhhc9<tm1Lex>	N	29944857
MGI:6315636	M	MP:0000781	decreased corpus callosum size	Zdhhc9<tm1Lex>/Y	B6.129S5-Zdhhc9<tm1Lex>	N	29944857
MGI:6315636	M	MP:0012307	impaired spatial learning	Zdhhc9<tm1Lex>/Y	B6.129S5-Zdhhc9<tm1Lex>	N	29944857
MGI:6315636	M	MP:0001364	decreased anxiety-related response	Zdhhc9<tm1Lex>/Y	B6.129S5-Zdhhc9<tm1Lex>	N	29944857
MGI:6315636	M	MP:0004144	hypotonia	Zdhhc9<tm1Lex>/Y	B6.129S5-Zdhhc9<tm1Lex>	N	29944857
MGI:6315641	M	MP:0002062	abnormal associative learning	Grm5<tm1Rod>/Grm5<tm1Rod>	B6.129-Grm5<tm1Rod>	N	30401923
MGI:6315641	M	MP:0012296	impaired discrimination learning	Grm5<tm1Rod>/Grm5<tm1Rod>	B6.129-Grm5<tm1Rod>	N	30401923
MGI:6315641	M	MP:0012315	impaired learning	Grm5<tm1Rod>/Grm5<tm1Rod>	B6.129-Grm5<tm1Rod>	N	30401923
MGI:6315641	M	MP:0014115	cognitive inflexibility	Grm5<tm1Rod>/Grm5<tm1Rod>	B6.129-Grm5<tm1Rod>	N	30401923
MGI:6315867	M	MP:0004753	abnormal miniature excitatory postsynaptic currents	Chrdl1<em1Nja>/Y	involves: C57BL/6J * DBA/2J	N	30344043
MGI:6315867	M	MP:0009538	abnormal synapse morphology	Chrdl1<em1Nja>/Y	involves: C57BL/6J * DBA/2J	N	30344043
MGI:6315867	M	MP:0004859	abnormal synaptic plasticity	Chrdl1<em1Nja>/Y	involves: C57BL/6J * DBA/2J	N	30344043
MGI:6315869	M	MP:0001262	decreased body weight	Lztr1<tm1a(EUCOMM)Wtsi>/Lztr1<+>	involves: C57BL/6N	N	30442762
MGI:6315869	M	MP:0008525	decreased cranium height	Lztr1<tm1a(EUCOMM)Wtsi>/Lztr1<+>	involves: C57BL/6N	N	30442762
MGI:6315869	M	MP:0005140	decreased cardiac muscle contractility	Lztr1<tm1a(EUCOMM)Wtsi>/Lztr1<+>	involves: C57BL/6N	N	30442762
MGI:6315869	F	MP:0011951	increased cardiac stroke volume	Lztr1<tm1a(EUCOMM)Wtsi>/Lztr1<+>	involves: C57BL/6N	N	30442762
MGI:6315869	M	MP:0003743	abnormal facial morphology	Lztr1<tm1a(EUCOMM)Wtsi>/Lztr1<+>	involves: C57BL/6N	N	30442762
MGI:6315995	M	MP:0003393	decreased cardiac output	Tg(Myh6-MYL3*E143K)2Dsc/0	Not Specified	N	28371863
MGI:6315995	M	MP:0011925	abnormal heart echocardiography feature	Tg(Myh6-MYL3*E143K)2Dsc/0	Not Specified	N	28371863
MGI:6315995	M	MP:0011952	decreased cardiac stroke volume	Tg(Myh6-MYL3*E143K)2Dsc/0	Not Specified	N	28371863
MGI:6316684	M	MP:0005386	behavior/neurological phenotype	Syap1<tm1a(EUCOMM)Hmgu>/Y	Not Specified	Y	31118165
MGI:6316684	M	MP:0010053	decreased grip strength	Syap1<tm1a(EUCOMM)Hmgu>/Y	Not Specified	N	31118165
MGI:6316684	M	MP:0001402	decreased locomotor activity	Syap1<tm1a(EUCOMM)Hmgu>/Y	Not Specified	N	31118165
MGI:6316684	M	MP:0001405	impaired coordination	Syap1<tm1a(EUCOMM)Hmgu>/Y	Not Specified	N	31118165
MGI:6316981	M	MP:0000747	muscle weakness	Col13a1<tm3.1Pih>/Col13a1<tm3.1Pih>	involves: 129S1/Sv * 129X1/SvJ	N	28369367
MGI:6317190	M	MP:0002757	decreased vertical activity	Tg(Prnp-MAPT*)2652Gds/0	B6.Cg-Tg(Prnp-MAPT*)2652Gds	N	26041339
MGI:6317190	M	MP:0001402	decreased locomotor activity	Tg(Prnp-MAPT*)2652Gds/0	B6.Cg-Tg(Prnp-MAPT*)2652Gds	N	26041339
MGI:6317390	F	MP:0014143	decreased body fat mass	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0001663	abnormal digestive system physiology	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0011503	distended jejunum	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0003949	abnormal circulating lipid level	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0010182	decreased susceptibility to weight gain	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0003271	abnormal duodenum morphology	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0003975	increased circulating VLDL triglyceride level	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0011881	distended duodenum	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0009485	distended ileum	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0000186	decreased circulating HDL cholesterol level	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	M	MP:0000186	decreased circulating HDL cholesterol level	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0010026	decreased liver cholesterol level	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0000496	abnormal small intestine morphology	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0010360	decreased liver free fatty acids level	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0003960	increased lean body mass	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0010155	abnormal intestine physiology	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0005341	decreased susceptibility to atherosclerosis	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0013957	increased small intestine length	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317390	F	MP:0020182	abnormal body mass index	Dennd5b<em1Smgo>/Dennd5b<em1Smgo>	involves: C57BL/6 * CBA	N	30837651
MGI:6317427	F	MP:0001566	increased circulating phosphate level	Klk5<tm2b(KOMP)Wtsi>/Klk5<tm2b(KOMP)Wtsi>	C57BL/6N-Klk5<tm2b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6317427	F	MP:0010067	increased red blood cell distribution width	Klk5<tm2b(KOMP)Wtsi>/Klk5<tm2b(KOMP)Wtsi>	C57BL/6N-Klk5<tm2b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6317427	F	MP:0010097	abnormal retina blood vessel morphology	Klk5<tm2b(KOMP)Wtsi>/Klk5<tm2b(KOMP)Wtsi>	C57BL/6N-Klk5<tm2b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6317427	F	MP:0002792	abnormal retina vasculature morphology	Klk5<tm2b(KOMP)Wtsi>/Klk5<tm2b(KOMP)Wtsi>	C57BL/6N-Klk5<tm2b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6317427	F	MP:0001402	decreased locomotor activity	Klk5<tm2b(KOMP)Wtsi>/Klk5<tm2b(KOMP)Wtsi>	C57BL/6N-Klk5<tm2b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6317427	M	MP:0001325	abnormal retina morphology	Klk5<tm2b(KOMP)Wtsi>/Klk5<tm2b(KOMP)Wtsi>	C57BL/6N-Klk5<tm2b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6317428	F	MP:0005419	decreased circulating serum albumin level	Wdsub1<tm1b(EUCOMM)Wtsi>/Wdsub1<+>	C57BL/6N-Wdsub1<tm1b(EUCOMM)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6317428	F	MP:0001303	abnormal lens morphology	Wdsub1<tm1b(EUCOMM)Wtsi>/Wdsub1<+>	C57BL/6N-Wdsub1<tm1b(EUCOMM)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6317428	F	MP:0001489	decreased startle reflex	Wdsub1<tm1b(EUCOMM)Wtsi>/Wdsub1<+>	C57BL/6N-Wdsub1<tm1b(EUCOMM)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6317428	F	MP:0005553	increased circulating creatinine level	Wdsub1<tm1b(EUCOMM)Wtsi>/Wdsub1<+>	C57BL/6N-Wdsub1<tm1b(EUCOMM)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6324209	M	MP:0010247	increased intestine copper level	Atp7a<Mo-blo>/Y	involves: C57BL/6J	N	6685755
MGI:6324209	M	MP:0003067	decreased liver copper level	Atp7a<Mo-blo>/Y	involves: C57BL/6J	N	6685755
MGI:6324209	M	MP:0003951	abnormal copper homeostasis	Atp7a<Mo-blo>/Y	involves: C57BL/6J	N	6685755
MGI:6324209	M	MP:0010243	increased kidney copper level	Atp7a<Mo-blo>/Y	involves: C57BL/6J	N	6685755
MGI:6324210	F	MP:0010243	increased kidney copper level	Atp7a<Mo-blo>/Atp7a<+>	involves: C57BL/6J	N	6685755
MGI:6324210	F	MP:0003951	abnormal copper homeostasis	Atp7a<Mo-blo>/Atp7a<+>	involves: C57BL/6J	N	6685755
MGI:6324210	F	MP:0001765	abnormal ion homeostasis	Atp7a<Mo-blo>/Atp7a<+>	involves: C57BL/6J	N	6685755
MGI:6324210	F	MP:0003067	decreased liver copper level	Atp7a<Mo-blo>/Atp7a<+>	involves: C57BL/6J	N	6685755
MGI:6324210	F	MP:0011215	decreased brain copper level	Atp7a<Mo-blo>/Atp7a<+>	involves: C57BL/6J	N	6685755
MGI:6324231	M	MP:0001274	curly vibrissae	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	MGI:60964
MGI:6324231	M	MP:0005171	absent coat pigmentation	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	MGI:60964
MGI:6324231	M	MP:0003067	decreased liver copper level	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	1819648
MGI:6324231	M	MP:0003067	decreased liver copper level	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	MGI:60964
MGI:6324231	M	MP:0001393	ataxia	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	MGI:60964
MGI:6324231	M	MP:0001731	abnormal postnatal growth	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	1819648
MGI:6324231	M	MP:0011215	decreased brain copper level	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	MGI:60964
MGI:6324231	M	MP:0011218	decreased brainstem copper level	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	MGI:60964
MGI:6324231	M	MP:0000489	abnormal large intestine morphology	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	MGI:60964
MGI:6324231	M	MP:0003952	abnormal copper level	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	MGI:60964
MGI:6324231	M	MP:0005584	abnormal enzyme/coenzyme activity	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	MGI:60964
MGI:6324231	M	MP:0010247	increased intestine copper level	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	MGI:60964
MGI:6324231	M	MP:0010243	increased kidney copper level	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	MGI:60964
MGI:6324231	M	MP:0005376	homeostasis/metabolism phenotype	Atp7a<Mo-ml>/Y	involves: C3Hf/He	Y	1819648
MGI:6324231	M	MP:0004953	decreased spleen weight	Atp7a<Mo-ml>/Y	involves: C3Hf/He	N	MGI:60964
MGI:6324238	F	MP:0001274	curly vibrissae	Atp7a<Mo-ml>/Atp7a<+>	involves: C3Hf/He	N	MGI:60964
MGI:6324238	F	MP:0010247	increased intestine copper level	Atp7a<Mo-ml>/Atp7a<+>	involves: C3Hf/He	N	MGI:60964
MGI:6324238	F	MP:0010016	variable depigmentation	Atp7a<Mo-ml>/Atp7a<+>	involves: C3Hf/He	N	MGI:60964
MGI:6324238	F	MP:0011215	decreased brain copper level	Atp7a<Mo-ml>/Atp7a<+>	involves: C3Hf/He	N	MGI:60964
MGI:6324256	F	MP:0003809	abnormal hair shaft morphology	Atp7a<Mo-to>/Atp7a<+>	B6.Cg-Atp7a<Mo-to>/J	N	7130053
MGI:6324256	F	MP:0010247	increased intestine copper level	Atp7a<Mo-to>/Atp7a<+>	B6.Cg-Atp7a<Mo-to>/J	N	7333461
MGI:6324256	F	MP:0001279	wavy vibrissae	Atp7a<Mo-to>/Atp7a<+>	B6.Cg-Atp7a<Mo-to>/J	N	7130053
MGI:6324372	M	MP:0003952	abnormal copper level	Atp7a<tm1.1Mjp>/Y,Mnx1<tm4(cre)Tmj>/Mnx1<+>	involves: 129S1/Sv * C57BL/6	N	25639447
MGI:6324372	M	MP:0001053	abnormal neuromuscular synapse morphology	Atp7a<tm1.1Mjp>/Y,Mnx1<tm4(cre)Tmj>/Mnx1<+>	involves: 129S1/Sv * C57BL/6	N	25639447
MGI:6324372	M	MP:0004819	decreased skeletal muscle mass	Atp7a<tm1.1Mjp>/Y,Mnx1<tm4(cre)Tmj>/Mnx1<+>	involves: 129S1/Sv * C57BL/6	N	25639447
MGI:6324372	M	MP:0002269	muscular atrophy	Atp7a<tm1.1Mjp>/Y,Mnx1<tm4(cre)Tmj>/Mnx1<+>	involves: 129S1/Sv * C57BL/6	N	25639447
MGI:6324372	M	MP:0001513	limb grasping	Atp7a<tm1.1Mjp>/Y,Mnx1<tm4(cre)Tmj>/Mnx1<+>	involves: 129S1/Sv * C57BL/6	N	25639447
MGI:6324372	M	MP:0001405	impaired coordination	Atp7a<tm1.1Mjp>/Y,Mnx1<tm4(cre)Tmj>/Mnx1<+>	involves: 129S1/Sv * C57BL/6	N	25639447
MGI:6324372	M	MP:0005335	abnormal gonadal fat pad morphology	Atp7a<tm1.1Mjp>/Y,Mnx1<tm4(cre)Tmj>/Mnx1<+>	involves: 129S1/Sv * C57BL/6	N	25639447
MGI:6324372	M	MP:0001406	abnormal gait	Atp7a<tm1.1Mjp>/Y,Mnx1<tm4(cre)Tmj>/Mnx1<+>	involves: 129S1/Sv * C57BL/6	N	25639447
MGI:6324372	M	MP:0000938	motor neuron degeneration	Atp7a<tm1.1Mjp>/Y,Mnx1<tm4(cre)Tmj>/Mnx1<+>	involves: 129S1/Sv * C57BL/6	N	25639447
MGI:6324372	M	MP:0010053	decreased grip strength	Atp7a<tm1.1Mjp>/Y,Mnx1<tm4(cre)Tmj>/Mnx1<+>	involves: 129S1/Sv * C57BL/6	N	25639447
MGI:6324372	M	MP:0002066	abnormal motor capabilities/coordination/movement	Atp7a<tm1.1Mjp>/Y,Mnx1<tm4(cre)Tmj>/Mnx1<+>	involves: 129S1/Sv * C57BL/6	N	25639447
MGI:6325103	M	MP:0002606	increased basophil cell number	Ace<tm1.1(KOMP)Vlcg>/Ace<+>	C57BL/6N-Ace<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325103	F	MP:0001399	hyperactivity	Ace<tm1.1(KOMP)Vlcg>/Ace<+>	C57BL/6N-Ace<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325107	M	MP:0000274	enlarged heart	Adamts9<tm1b(KOMP)Wtsi>/Adamts9<+>	C57BL/6N-Adamts9<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325107	F	MP:0002339	abnormal lymph node morphology	Adamts9<tm1b(KOMP)Wtsi>/Adamts9<+>	C57BL/6N-Adamts9<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325107	M	MP:0000266	abnormal heart morphology	Adamts9<tm1b(KOMP)Wtsi>/Adamts9<+>	C57BL/6N-Adamts9<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325107	F	MP:0002092	abnormal eye morphology	Adamts9<tm1b(KOMP)Wtsi>/Adamts9<+>	C57BL/6N-Adamts9<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325108	M	MP:0011100	preweaning lethality, complete penetrance	Adamts9<tm1b(KOMP)Wtsi>/Adamts9<tm1b(KOMP)Wtsi>	C57BL/6N-Adamts9<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325109	F	MP:0001304	cataract	Angptl1<tm4b(KOMP)Wtsi>/Angptl1<tm4b(KOMP)Wtsi>	C57BL/6N-Angptl1<tm4b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325109	F	MP:0005565	increased blood urea nitrogen level	Angptl1<tm4b(KOMP)Wtsi>/Angptl1<tm4b(KOMP)Wtsi>	C57BL/6N-Angptl1<tm4b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325109	F	MP:0001303	abnormal lens morphology	Angptl1<tm4b(KOMP)Wtsi>/Angptl1<tm4b(KOMP)Wtsi>	C57BL/6N-Angptl1<tm4b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325110	F	MP:0000689	abnormal spleen morphology	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325110	F	MP:0002135	abnormal kidney morphology	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325110	M	MP:0001146	abnormal testis morphology	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325110	M	MP:0010123	increased bone mineral content	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325110	F	MP:0010067	increased red blood cell distribution width	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325110	F	MP:0000691	enlarged spleen	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325110	M	MP:0003960	increased lean body mass	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325110	M	MP:0001147	small testis	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325110	M	MP:0010025	decreased total body fat amount	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325110	F	MP:0005562	decreased mean corpuscular hemoglobin	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325110	F	MP:0010053	decreased grip strength	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325110	M	MP:0003917	increased kidney weight	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325110	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325111	M	MP:0001489	decreased startle reflex	Aqp9<tm1b(KOMP)Wtsi>/Aqp9<tm1b(KOMP)Wtsi>	C57BL/6N-Aqp9<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325111	M	MP:0000558	abnormal tibia morphology	Aqp9<tm1b(KOMP)Wtsi>/Aqp9<tm1b(KOMP)Wtsi>	C57BL/6N-Aqp9<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325111	M	MP:0002764	short tibia	Aqp9<tm1b(KOMP)Wtsi>/Aqp9<tm1b(KOMP)Wtsi>	C57BL/6N-Aqp9<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325112	F	MP:0008074	increased CD4-positive, alpha-beta T cell number	Asb2<tm2b(KOMP)Wtsi>/Asb2<+>	C57BL/6N-Asb2<tm2b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325112	M	MP:0010025	decreased total body fat amount	Asb2<tm2b(KOMP)Wtsi>/Asb2<+>	C57BL/6N-Asb2<tm2b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325112	M	MP:0005343	increased circulating aspartate transaminase level	Asb2<tm2b(KOMP)Wtsi>/Asb2<+>	C57BL/6N-Asb2<tm2b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325112	M	MP:0010097	abnormal retina blood vessel morphology	Asb2<tm2b(KOMP)Wtsi>/Asb2<+>	C57BL/6N-Asb2<tm2b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325116	F	MP:0001697	abnormal embryo size	Bmi1<tm1.1(KOMP)Vlcg>/Bmi1<+>	C57BL/6N-Bmi1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325116	F	MP:0001293	anophthalmia	Bmi1<tm1.1(KOMP)Vlcg>/Bmi1<+>	C57BL/6N-Bmi1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325119	M	MP:0001697	abnormal embryo size	Casc3<tm1.1(KOMP)Vlcg>/Casc3<tm1.1(KOMP)Vlcg>	C57BL/6N-Casc3<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325125	M	MP:0001785	edema	Cnr1<tm1.1(KOMP)Vlcg>/Cnr1<+>	C57BL/6N-Cnr1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325128	M	MP:0011100	preweaning lethality, complete penetrance	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<tm1b(KOMP)Wtsi>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325131	F	MP:0002075	abnormal coat/hair pigmentation	Edem3<tm1b(EUCOMM)Hmgu>/Edem3<+>	C57BL/6N-Edem3<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:6325131	F	MP:0000063	decreased bone mineral density	Edem3<tm1b(EUCOMM)Hmgu>/Edem3<+>	C57BL/6N-Edem3<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:6325132	M	MP:0003960	increased lean body mass	Erap1<tm2b(EUCOMM)Wtsi>/Erap1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Erap1<tm2b(EUCOMM)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325132	M	MP:0001399	hyperactivity	Erap1<tm2b(EUCOMM)Wtsi>/Erap1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Erap1<tm2b(EUCOMM)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325132	M	MP:0010025	decreased total body fat amount	Erap1<tm2b(EUCOMM)Wtsi>/Erap1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Erap1<tm2b(EUCOMM)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325132	F	MP:0010124	decreased bone mineral content	Erap1<tm2b(EUCOMM)Wtsi>/Erap1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Erap1<tm2b(EUCOMM)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325132	F	MP:0000194	increased circulating calcium level	Erap1<tm2b(EUCOMM)Wtsi>/Erap1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Erap1<tm2b(EUCOMM)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325132	M	MP:0005419	decreased circulating serum albumin level	Erap1<tm2b(EUCOMM)Wtsi>/Erap1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Erap1<tm2b(EUCOMM)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325132	M	MP:0000598	abnormal liver morphology	Erap1<tm2b(EUCOMM)Wtsi>/Erap1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Erap1<tm2b(EUCOMM)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325132	M	MP:0005505	thrombocytosis	Erap1<tm2b(EUCOMM)Wtsi>/Erap1<tm2b(EUCOMM)Wtsi>	C57BL/6N-Erap1<tm2b(EUCOMM)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325137	M	MP:0001891	hydrocephaly	Fgf15<tm1.1(KOMP)Vlcg>/Fgf15<+>	C57BL/6N-Fgf15<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325137	M	MP:0002152	abnormal brain morphology	Fgf15<tm1.1(KOMP)Vlcg>/Fgf15<+>	C57BL/6N-Fgf15<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325139	M	MP:0001314	cornea opacity	Fkbp5<tm1b(KOMP)Wtsi>/Fkbp5<tm1b(KOMP)Wtsi>	C57BL/6N-Fkbp5<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325139	M	MP:0002606	increased basophil cell number	Fkbp5<tm1b(KOMP)Wtsi>/Fkbp5<tm1b(KOMP)Wtsi>	C57BL/6N-Fkbp5<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325139	M	MP:0003917	increased kidney weight	Fkbp5<tm1b(KOMP)Wtsi>/Fkbp5<tm1b(KOMP)Wtsi>	C57BL/6N-Fkbp5<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325139	M	MP:0000219	increased neutrophil cell number	Fkbp5<tm1b(KOMP)Wtsi>/Fkbp5<tm1b(KOMP)Wtsi>	C57BL/6N-Fkbp5<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325144	F	MP:0009709	hydrometra	Gpx4<tm1.1(KOMP)Vlcg>/Gpx4<+>	C57BL/6N-Gpx4<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325147	M	MP:0000897	abnormal midbrain morphology	Inpp5e<tm1.1(KOMP)Vlcg>/Inpp5e<tm1.1(KOMP)Vlcg>	C57BL/6N-Inpp5e<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325147	M	MP:0003720	abnormal neural tube closure	Inpp5e<tm1.1(KOMP)Vlcg>/Inpp5e<tm1.1(KOMP)Vlcg>	C57BL/6N-Inpp5e<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325147	M	MP:0002092	abnormal eye morphology	Inpp5e<tm1.1(KOMP)Vlcg>/Inpp5e<tm1.1(KOMP)Vlcg>	C57BL/6N-Inpp5e<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325147	M	MP:0000841	abnormal hindbrain morphology	Inpp5e<tm1.1(KOMP)Vlcg>/Inpp5e<tm1.1(KOMP)Vlcg>	C57BL/6N-Inpp5e<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325147	M	MP:0000783	abnormal forebrain morphology	Inpp5e<tm1.1(KOMP)Vlcg>/Inpp5e<tm1.1(KOMP)Vlcg>	C57BL/6N-Inpp5e<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325148	F	MP:0001257	increased body length	Irx6<tm1b(KOMP)Mbp>/Irx6<tm1b(KOMP)Mbp>	C57BL/6N-Irx6<tm1b(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:6325148	M	MP:0002075	abnormal coat/hair pigmentation	Irx6<tm1b(KOMP)Mbp>/Irx6<tm1b(KOMP)Mbp>	C57BL/6N-Irx6<tm1b(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:6325148	M	MP:0000598	abnormal liver morphology	Irx6<tm1b(KOMP)Mbp>/Irx6<tm1b(KOMP)Mbp>	C57BL/6N-Irx6<tm1b(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:6325148	M	MP:0002059	abnormal seminal vesicle morphology	Irx6<tm1b(KOMP)Mbp>/Irx6<tm1b(KOMP)Mbp>	C57BL/6N-Irx6<tm1b(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:6325148	F	MP:0002092	abnormal eye morphology	Irx6<tm1b(KOMP)Mbp>/Irx6<tm1b(KOMP)Mbp>	C57BL/6N-Irx6<tm1b(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:6325148	M	MP:0001566	increased circulating phosphate level	Irx6<tm1b(KOMP)Mbp>/Irx6<tm1b(KOMP)Mbp>	C57BL/6N-Irx6<tm1b(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:6325160	F	MP:0001488	increased startle reflex	Npas3<tm1b(KOMP)Wtsi>/Npas3<+>	C57BL/6N-Npas3<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325161	M	MP:0002764	short tibia	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325164	F	MP:0010379	decreased respiratory quotient	Phgdh<tm1b(KOMP)Wtsi>/Phgdh<+>	C57BL/6N-Phgdh<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325164	F	MP:0011940	decreased food intake	Phgdh<tm1b(KOMP)Wtsi>/Phgdh<+>	C57BL/6N-Phgdh<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325164	F	MP:0011942	decreased fluid intake	Phgdh<tm1b(KOMP)Wtsi>/Phgdh<+>	C57BL/6N-Phgdh<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325168	M	MP:0005505	thrombocytosis	Ppp4r1<em1(IMPC)Rbrc>/Ppp4r1<em1(IMPC)Rbrc>	C57BL/6N-Ppp4r1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:6325168	M	MP:0001925	male infertility	Ppp4r1<em1(IMPC)Rbrc>/Ppp4r1<em1(IMPC)Rbrc>	C57BL/6N-Ppp4r1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:6325169	M	MP:0020420	abnormal freezing behavior	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325169	M	MP:0000186	decreased circulating HDL cholesterol level	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325169	M	MP:0005179	decreased circulating cholesterol level	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325169	M	MP:0009454	impaired contextual conditioning behavior	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325179	F	MP:0003960	increased lean body mass	Slc7a7<em1(IMPC)Bay>/Slc7a7<+>	C57BL/6N-Slc7a7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6325180	F	MP:0004258	abnormal placenta size	Slc7a7<em1(IMPC)Bay>/Slc7a7<em1(IMPC)Bay>	C57BL/6N-Slc7a7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6325180	F	MP:0003984	embryonic growth retardation	Slc7a7<em1(IMPC)Bay>/Slc7a7<em1(IMPC)Bay>	C57BL/6N-Slc7a7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6325180	F	MP:0001697	abnormal embryo size	Slc7a7<em1(IMPC)Bay>/Slc7a7<em1(IMPC)Bay>	C57BL/6N-Slc7a7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6325181	F	MP:0000428	abnormal craniofacial morphology	Snx27<tm1b(KOMP)Wtsi>/Snx27<tm1b(KOMP)Wtsi>	C57BL/6N-Snx27<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6325183	M	MP:0003984	embryonic growth retardation	St14<tm1.1(KOMP)Vlcg>/St14<tm1.1(KOMP)Vlcg>	C57BL/6N-St14<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6325184	M	MP:0003960	increased lean body mass	Tmem72<tm1b(KOMP)Wtsi>/Tmem72<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem72<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325184	F	MP:0001566	increased circulating phosphate level	Tmem72<tm1b(KOMP)Wtsi>/Tmem72<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem72<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325184	M	MP:0001488	increased startle reflex	Tmem72<tm1b(KOMP)Wtsi>/Tmem72<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem72<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325184	F	MP:0003131	increased erythrocyte cell number	Tmem72<tm1b(KOMP)Wtsi>/Tmem72<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem72<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325184	M	MP:0002075	abnormal coat/hair pigmentation	Tmem72<tm1b(KOMP)Wtsi>/Tmem72<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem72<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6325185	M	MP:0002339	abnormal lymph node morphology	Tmem86a<tm1b(KOMP)Mbp>/Tmem86a<tm1b(KOMP)Mbp>	C57BL/6N-Tmem86a<tm1b(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:6325185	M	MP:0002059	abnormal seminal vesicle morphology	Tmem86a<tm1b(KOMP)Mbp>/Tmem86a<tm1b(KOMP)Mbp>	C57BL/6N-Tmem86a<tm1b(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:6325185	F	MP:0002764	short tibia	Tmem86a<tm1b(KOMP)Mbp>/Tmem86a<tm1b(KOMP)Mbp>	C57BL/6N-Tmem86a<tm1b(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:6325185	F	MP:0005565	increased blood urea nitrogen level	Tmem86a<tm1b(KOMP)Mbp>/Tmem86a<tm1b(KOMP)Mbp>	C57BL/6N-Tmem86a<tm1b(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:6330781	F	MP:0001392	abnormal locomotor behavior	Pth2r<tm1.1Tbu>/Pth2r<tm1.1Tbu>	involves: 129 * 129S4/SvJae * C57BL/6	N	28890271
MGI:6330781	F	MP:0003360	abnormal depression-related behavior	Pth2r<tm1.1Tbu>/Pth2r<tm1.1Tbu>	involves: 129 * 129S4/SvJae * C57BL/6	N	28890271
MGI:6330781	F	MP:0001442	decreased grooming behavior	Pth2r<tm1.1Tbu>/Pth2r<tm1.1Tbu>	involves: 129 * 129S4/SvJae * C57BL/6	N	28890271
MGI:6330781	F	MP:0020477	abnormal locomotor circadian rhythm	Pth2r<tm1.1Tbu>/Pth2r<tm1.1Tbu>	involves: 129 * 129S4/SvJae * C57BL/6	N	28890271
MGI:6330781	F	MP:0011014	decreased core body temperature	Pth2r<tm1.1Tbu>/Pth2r<tm1.1Tbu>	involves: 129 * 129S4/SvJae * C57BL/6	N	28890271
MGI:6330781	F	MP:0005386	behavior/neurological phenotype	Pth2r<tm1.1Tbu>/Pth2r<tm1.1Tbu>	involves: 129 * 129S4/SvJae * C57BL/6	Y	28890271
MGI:6330781	F	MP:0004924	abnormal behavior	Pth2r<tm1.1Tbu>/Pth2r<tm1.1Tbu>	involves: 129 * 129S4/SvJae * C57BL/6	N	28890271
MGI:6332960	M	MP:0001407	short stride length	Sgce<Gt(148G1)Cmhd>/Sgce<+>	B6.129-Sgce<Gt(148G1)Cmhd>	N	27890709
MGI:6336223	M	MP:0000495	abnormal colon morphology	Tfr2<em1(IMPC)Rbrc>/Tfr2<em1(IMPC)Rbrc>	C57BL/6N-Tfr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:6336223	M	MP:0000598	abnormal liver morphology	Tfr2<em1(IMPC)Rbrc>/Tfr2<em1(IMPC)Rbrc>	C57BL/6N-Tfr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:6336223	F	MP:0000226	abnormal mean corpuscular volume	Tfr2<em1(IMPC)Rbrc>/Tfr2<em1(IMPC)Rbrc>	C57BL/6N-Tfr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:6336223	M	MP:0000492	abnormal rectum morphology	Tfr2<em1(IMPC)Rbrc>/Tfr2<em1(IMPC)Rbrc>	C57BL/6N-Tfr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:6336223	M	MP:0000274	enlarged heart	Tfr2<em1(IMPC)Rbrc>/Tfr2<em1(IMPC)Rbrc>	C57BL/6N-Tfr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:6336223	M	MP:0000266	abnormal heart morphology	Tfr2<em1(IMPC)Rbrc>/Tfr2<em1(IMPC)Rbrc>	C57BL/6N-Tfr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:6336223	F	MP:0005640	abnormal mean corpuscular hemoglobin concentration	Tfr2<em1(IMPC)Rbrc>/Tfr2<em1(IMPC)Rbrc>	C57BL/6N-Tfr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:6336223	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Tfr2<em1(IMPC)Rbrc>/Tfr2<em1(IMPC)Rbrc>	C57BL/6N-Tfr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:6336223	F	MP:0005563	abnormal hemoglobin content	Tfr2<em1(IMPC)Rbrc>/Tfr2<em1(IMPC)Rbrc>	C57BL/6N-Tfr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:6336223	F	MP:0001586	abnormal erythrocyte cell number	Tfr2<em1(IMPC)Rbrc>/Tfr2<em1(IMPC)Rbrc>	C57BL/6N-Tfr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:6336223	F	MP:0001589	abnormal mean corpuscular hemoglobin	Tfr2<em1(IMPC)Rbrc>/Tfr2<em1(IMPC)Rbrc>	C57BL/6N-Tfr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:6342278	M	MP:0000111	cleft palate	H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Piga<tm1Tak>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	N	31232685
MGI:6342278	M	MP:0002116	abnormal craniofacial bone morphology	H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Piga<tm1Tak>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	N	31232685
MGI:6342278	M	MP:0005170	cleft upper lip	H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Piga<tm1Tak>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	N	31232685
MGI:6343571	M	MP:0005404	abnormal axon morphology	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>	involves: C57BL/6N	N	30520996
MGI:6343571	M	MP:0004768	abnormal axonal transport	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>	involves: C57BL/6N	N	30520996
MGI:6343571	M	MP:0001513	limb grasping	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>	involves: C57BL/6N	N	30520996
MGI:6343571	M	MP:0002878	abnormal corticospinal tract morphology	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>	involves: C57BL/6N	N	30520996
MGI:6343571	M	MP:0000955	abnormal spinal cord morphology	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>	involves: C57BL/6N	N	30520996
MGI:6343571	M	MP:0001263	weight loss	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>	involves: C57BL/6N	N	30520996
MGI:6343571	M	MP:0005405	axon degeneration	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>	involves: C57BL/6N	N	30520996
MGI:6343571	M	MP:0000745	tremors	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>	involves: C57BL/6N	N	30520996
MGI:6343572	M	MP:0001513	limb grasping	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<+>	involves: C57BL/6N	N	30520996
MGI:6343572	M	MP:0005405	axon degeneration	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<+>	involves: C57BL/6N	N	30520996
MGI:6343572	M	MP:0004768	abnormal axonal transport	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<+>	involves: C57BL/6N	N	30520996
MGI:6343572	M	MP:0000955	abnormal spinal cord morphology	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<+>	involves: C57BL/6N	N	30520996
MGI:6343572	M	MP:0002878	abnormal corticospinal tract morphology	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<+>	involves: C57BL/6N	N	30520996
MGI:6343572	M	MP:0001263	weight loss	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<+>	involves: C57BL/6N	N	30520996
MGI:6343572	M	MP:0000745	tremors	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<+>	involves: C57BL/6N	N	30520996
MGI:6343572	M	MP:0005404	abnormal axon morphology	Gt(ROSA)26Sor<tm1.1(CAG-SPAST*C448Y)Baas>/Gt(ROSA)26Sor<+>	involves: C57BL/6N	N	30520996
MGI:6356398	M	MP:0003333	liver fibrosis	Lepr<db>/Lepr<db>	B6.BKS(D)-Lepr<db>/JOrlRj	N	22118645
MGI:6356398	M	MP:0005658	increased susceptibility to diet-induced obesity	Lepr<db>/Lepr<db>	B6.BKS(D)-Lepr<db>/JOrlRj	N	22118645
MGI:6356398	M	MP:0001260	increased body weight	Lepr<db>/Lepr<db>	B6.BKS(D)-Lepr<db>/JOrlRj	N	22118645
MGI:6356398	M	MP:0002628	hepatic steatosis	Lepr<db>/Lepr<db>	B6.BKS(D)-Lepr<db>/JOrlRj	N	22118645
MGI:6356398	M	MP:0003887	increased hepatocyte apoptosis	Lepr<db>/Lepr<db>	B6.BKS(D)-Lepr<db>/JOrlRj	N	22118645
MGI:6356398	M	MP:0003982	increased cholesterol level	Lepr<db>/Lepr<db>	B6.BKS(D)-Lepr<db>/JOrlRj	N	22118645
MGI:6356398	M	MP:0001860	liver inflammation	Lepr<db>/Lepr<db>	B6.BKS(D)-Lepr<db>/JOrlRj	N	22118645
MGI:6356398	M	MP:0002575	increased circulating ketone body level	Lepr<db>/Lepr<db>	B6.BKS(D)-Lepr<db>/JOrlRj	N	22118645
MGI:6356523	M	MP:0000063	decreased bone mineral density	Hvf/Hvf<+>	involves: C3H/HeH * C57BL/6J	N	30283900
MGI:6356633	M	MP:0001258	decreased body length	Rit1<tm1.1Tumg>/Rit1<+>	B6.Cg-Rit1<tm1.1Tumg>	N	30898653
MGI:6356633	F	MP:0001923	reduced female fertility	Rit1<tm1.1Tumg>/Rit1<+>	B6.Cg-Rit1<tm1.1Tumg>	N	30898653
MGI:6357674	M	MP:0003666	impaired sperm capacitation	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	27811987
MGI:6357674	M	MP:0003666	impaired sperm capacitation	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	34704967
MGI:6357674	M	MP:0031012	impaired sperm migration in female genital tract	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	27811987
MGI:6357674	M	MP:0001922	reduced male fertility	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	27811987
MGI:6357674	M	MP:0002675	asthenozoospermia	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	34704967
MGI:6357674	M	MP:0002675	asthenozoospermia	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	27811987
MGI:6357674	M	MP:0020451	decreased sperm progressive motility	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	27811987
MGI:6357674	M	MP:0004043	abnormal pH regulation	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	34704967
MGI:6357674	M	MP:0000242	impaired fertilization	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	27811987
MGI:6357674	M	MP:0009834	abnormal sperm annulus morphology	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	27811987
MGI:6357674	M	MP:0009647	decreased fertilization frequency	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	34704967
MGI:6357674	M	MP:0008892	abnormal sperm flagellum morphology	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	27811987
MGI:6357674	M	MP:0008892	abnormal sperm flagellum morphology	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	34704967
MGI:6357674	M	MP:0001765	abnormal ion homeostasis	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	34704967
MGI:6357674	F	MP:0005389	reproductive system phenotype	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	Y	27811987
MGI:6357674	M	MP:0009237	kinked sperm flagellum	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	27811987
MGI:6357674	M	MP:0009243	hairpin sperm flagellum	Slc22a14<em1Fjw>/Slc22a14<em1Fjw>	involves: C57BL/6N	N	27811987
MGI:6357695	M	MP:0011965	decreased total retina thickness	Atp6ap2<tm1.1Aich>/Y,Tg(Crx-cre)1Tfur/0	involves: C57BL/6	N	24305829
MGI:6357695	M	MP:0008450	retina photoreceptor degeneration	Atp6ap2<tm1.1Aich>/Y,Tg(Crx-cre)1Tfur/0	involves: C57BL/6	N	24305829
MGI:6357695	M	MP:0012144	decreased b-wave amplitude	Atp6ap2<tm1.1Aich>/Y,Tg(Crx-cre)1Tfur/0	involves: C57BL/6	N	24305829
MGI:6357695	M	MP:0001325	abnormal retina morphology	Atp6ap2<tm1.1Aich>/Y,Tg(Crx-cre)1Tfur/0	involves: C57BL/6	N	24305829
MGI:6357695	M	MP:0003727	abnormal retina layer morphology	Atp6ap2<tm1.1Aich>/Y,Tg(Crx-cre)1Tfur/0	involves: C57BL/6	N	24305829
MGI:6357695	M	MP:0012143	decreased a-wave amplitude	Atp6ap2<tm1.1Aich>/Y,Tg(Crx-cre)1Tfur/0	involves: C57BL/6	N	24305829
MGI:6357730	F	MP:0004860	dilated kidney collecting duct	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0003918	decreased kidney weight	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0000521	abnormal kidney cortex morphology	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0006032	abnormal ureteric bud morphology	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0011290	decreased nephron number	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0001762	polyuria	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0003675	kidney cyst	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0004754	abnormal kidney collecting duct morphology	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0002989	small kidney	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0004936	impaired branching involved in ureteric bud morphogenesis	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0002988	decreased urine osmolality	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0003446	renal hypoplasia	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0009349	increased urine pH	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0011457	abnormal metanephric ureteric bud development	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357730	F	MP:0005553	increased circulating creatinine level	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Hoxb7-cre)5526Cmb/0	involves: C57BL/6	N	23704941
MGI:6357739	F	MP:0003918	decreased kidney weight	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0004936	impaired branching involved in ureteric bud morphogenesis	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0011307	kidney medulla cyst	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0011085	postnatal lethality, complete penetrance	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0002989	small kidney	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0011334	abnormal nephrogenic zone morphology	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0005325	abnormal renal glomerulus morphology	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0010984	abnormal metanephric mesenchyme morphology	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0000521	abnormal kidney cortex morphology	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0000522	kidney cortex cyst	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0000527	abnormal kidney development	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0012026	abnormal S-shaped body morphology	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0011290	decreased nephron number	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0012025	abnormal comma shaped body morphology	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0003881	abnormal nephron morphology	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0008140	podocyte foot process effacement	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357739	F	MP:0012024	abnormal nephron morphogenesis	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357740	F	MP:0003918	decreased kidney weight	Atp6ap2<tm1.1Aich>/Atp6ap2<+>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357740	F	MP:0005553	increased circulating creatinine level	Atp6ap2<tm1.1Aich>/Atp6ap2<+>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357740	F	MP:0002871	albuminuria	Atp6ap2<tm1.1Aich>/Atp6ap2<+>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357740	F	MP:0005264	glomerulosclerosis	Atp6ap2<tm1.1Aich>/Atp6ap2<+>,Tg(Six2-EGFP/cre)1Amc/0	involves: C57BL/6 * CD-1	N	26658320
MGI:6357744	F	MP:0000607	abnormal hepatocyte morphology	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6 * C57BL/6J * CBA/J	N	28129027
MGI:6357744	F	MP:0010080	abnormal hepatocyte physiology	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6 * C57BL/6J * CBA/J	N	28129027
MGI:6357744	F	MP:0030940	impaired autophagy	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6 * C57BL/6J * CBA/J	N	28129027
MGI:6357744	F	MP:0000599	enlarged liver	Atp6ap2<tm1.1Aich>/Atp6ap2<tm1.1Aich>,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6 * C57BL/6J * CBA/J	N	28129027
MGI:6357747	M	MP:0000599	enlarged liver	Atp6ap2<tm1.1Aich>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6 * C57BL/6J * CBA/J	N	28129027
MGI:6357747	M	MP:0000607	abnormal hepatocyte morphology	Atp6ap2<tm1.1Aich>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6 * C57BL/6J * CBA/J	N	28129027
MGI:6357747	M	MP:0010080	abnormal hepatocyte physiology	Atp6ap2<tm1.1Aich>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6 * C57BL/6J * CBA/J	N	28129027
MGI:6357747	M	MP:0030940	impaired autophagy	Atp6ap2<tm1.1Aich>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6 * C57BL/6J * CBA/J	N	28129027
MGI:6357843	M	MP:0009831	abnormal sperm midpiece morphology	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	M	MP:0009239	short sperm flagellum	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	M	MP:0009237	kinked sperm flagellum	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	M	MP:0031356	abnormal outer dense fiber morphology	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	F	MP:0005389	reproductive system phenotype	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	Y	30683861
MGI:6357843	M	MP:0008892	abnormal sperm flagellum morphology	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	M	MP:0001925	male infertility	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	M	MP:0008545	absent sperm flagellum	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	M	MP:0020451	decreased sperm progressive motility	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	M	MP:0004929	decreased epididymis weight	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	M	MP:0009238	coiled sperm flagellum	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	M	MP:0002675	asthenozoospermia	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	M	MP:0009838	abnormal sperm axoneme morphology	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	M	MP:0009836	abnormal sperm principal piece morphology	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	M	MP:0002687	oligozoospermia	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357843	M	MP:0004930	small epididymis	Qrich2<em1Xdz>/Qrich2<em1Xdz>	involves: C57BL/6J	N	30683861
MGI:6357844	M	MP:0005389	reproductive system phenotype	Qrich2<em1Xdz>/Qrich2<+>	involves: C57BL/6J	Y	30683861
MGI:6357844	M	MP:0002675	asthenozoospermia	Qrich2<em1Xdz>/Qrich2<+>	involves: C57BL/6J	N	30683861
MGI:6357844	M	MP:0020451	decreased sperm progressive motility	Qrich2<em1Xdz>/Qrich2<+>	involves: C57BL/6J	N	30683861
MGI:6357844	M	MP:0002687	oligozoospermia	Qrich2<em1Xdz>/Qrich2<+>	involves: C57BL/6J	N	30683861
MGI:6357855	M	MP:0001156	abnormal spermatogenesis	Ggnbp2<tm1Bbs>/Ggnbp2<tm1Bbs>	involves: 129S6/SvEvTac * C57BL/6	N	28592902
MGI:6357855	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Ggnbp2<tm1Bbs>/Ggnbp2<tm1Bbs>	involves: 129S6/SvEvTac * C57BL/6	N	28592902
MGI:6357855	M	MP:0013601	increased testis apoptosis	Ggnbp2<tm1Bbs>/Ggnbp2<tm1Bbs>	involves: 129S6/SvEvTac * C57BL/6	N	28592902
MGI:6357855	M	MP:0001925	male infertility	Ggnbp2<tm1Bbs>/Ggnbp2<tm1Bbs>	involves: 129S6/SvEvTac * C57BL/6	N	28592902
MGI:6357855	M	MP:0002216	abnormal seminiferous tubule morphology	Ggnbp2<tm1Bbs>/Ggnbp2<tm1Bbs>	involves: 129S6/SvEvTac * C57BL/6	N	28592902
MGI:6357855	M	MP:0005159	azoospermia	Ggnbp2<tm1Bbs>/Ggnbp2<tm1Bbs>	involves: 129S6/SvEvTac * C57BL/6	N	28592902
MGI:6357855	M	MP:0005250	decreased Sertoli cell number	Ggnbp2<tm1Bbs>/Ggnbp2<tm1Bbs>	involves: 129S6/SvEvTac * C57BL/6	N	28592902
MGI:6357857	M	MP:0001405	impaired coordination	Coa8<em1Zev>/Coa8<em1Zev>	FVB/NJ-Coa8<em1Zev>	N	30552096
MGI:6357857	F	MP:0001405	impaired coordination	Coa8<em1Zev>/Coa8<em1Zev>	FVB/NJ-Coa8<em1Zev>	N	30552096
MGI:6357922	M	MP:0003631	nervous system phenotype	Arhgap36<em1Seul>/Y	Not Specified	Y	31305241
MGI:6357924	F	MP:0009684	abnormal spinal cord lateral motor column morphology	Arhgap36<em1Seul>/Arhgap36<em1Seul>	Not Specified	N	31305241
MGI:6357924	F	MP:0003631	nervous system phenotype	Arhgap36<em1Seul>/Arhgap36<em1Seul>	Not Specified	Y	31305241
MGI:6358169	M	MP:0003354	astrocytosis	Alg13<em1Bayu>/Y	involves: C57BL/6J	N	30872163
MGI:6358169	M	MP:0003240	loss of hippocampal neurons	Alg13<em1Bayu>/Y	involves: C57BL/6J	N	30872163
MGI:6358169	M	MP:0004859	abnormal synaptic plasticity	Alg13<em1Bayu>/Y	involves: C57BL/6J	N	30872163
MGI:6358169	M	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality	Alg13<em1Bayu>/Y	involves: C57BL/6J	N	30872163
MGI:6358169	M	MP:0002906	increased susceptibility to pharmacologically induced seizures	Alg13<em1Bayu>/Y	involves: C57BL/6J	N	30872163
MGI:6358169	M	MP:0009358	environmentally induced seizures	Alg13<em1Bayu>/Y	involves: C57BL/6J	N	30872163
MGI:6358239	M	MP:0009647	decreased fertilization frequency	Prss55<tm1Zgwg>/Prss55<tm1Zgwg>	involves: 129 * C57BL/6	N	30032357
MGI:6358239	M	MP:0030978	impaired binding of sperm to zona pellucida	Prss55<tm1Zgwg>/Prss55<tm1Zgwg>	involves: 129 * C57BL/6	N	30032357
MGI:6358239	M	MP:0001925	male infertility	Prss55<tm1Zgwg>/Prss55<tm1Zgwg>	involves: 129 * C57BL/6	N	30032357
MGI:6358239	M	MP:0031012	impaired sperm migration in female genital tract	Prss55<tm1Zgwg>/Prss55<tm1Zgwg>	involves: 129 * C57BL/6	N	30032357
MGI:6358362	F	MP:0001885	mammary gland duct hyperplasia	Tg(KRT5-rtTA)#Glk/0,Tg(tetO-Mir31)#Zhyu/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358362	F	MP:0009506	abnormal mammary gland alveolus morphology	Tg(KRT5-rtTA)#Glk/0,Tg(tetO-Mir31)#Zhyu/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358362	F	MP:0010173	increased mammary gland epithelial cell proliferation	Tg(KRT5-rtTA)#Glk/0,Tg(tetO-Mir31)#Zhyu/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358362	F	MP:0000630	mammary gland hyperplasia	Tg(KRT5-rtTA)#Glk/0,Tg(tetO-Mir31)#Zhyu/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358362	F	MP:0006269	abnormal mammary gland growth during pregnancy	Tg(KRT5-rtTA)#Glk/0,Tg(tetO-Mir31)#Zhyu/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358362	F	MP:0009504	abnormal mammary gland epithelium morphology	Tg(KRT5-rtTA)#Glk/0,Tg(tetO-Mir31)#Zhyu/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358362	F	MP:0001382	abnormal nursing	Tg(KRT5-rtTA)#Glk/0,Tg(tetO-Mir31)#Zhyu/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358362	F	MP:0009503	abnormal mammary gland duct morphology	Tg(KRT5-rtTA)#Glk/0,Tg(tetO-Mir31)#Zhyu/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358362	F	MP:0000662	abnormal branching of the mammary ductal tree	Tg(KRT5-rtTA)#Glk/0,Tg(tetO-Mir31)#Zhyu/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358362	F	MP:0000628	abnormal mammary gland development	Tg(KRT5-rtTA)#Glk/0,Tg(tetO-Mir31)#Zhyu/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358362	F	MP:0000627	abnormal mammary gland morphology	Tg(KRT5-rtTA)#Glk/0,Tg(tetO-Mir31)#Zhyu/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358363	F	MP:0001881	abnormal mammary gland physiology	Mir31<em1Nju>/Mir31<em1Nju>	involves: C57BL/6J	N	29051494
MGI:6358363	F	MP:0006269	abnormal mammary gland growth during pregnancy	Mir31<em1Nju>/Mir31<em1Nju>	involves: C57BL/6J	N	29051494
MGI:6358363	F	MP:0009506	abnormal mammary gland alveolus morphology	Mir31<em1Nju>/Mir31<em1Nju>	involves: C57BL/6J	N	29051494
MGI:6358363	F	MP:0013716	hypolactation	Mir31<em1Nju>/Mir31<em1Nju>	involves: C57BL/6J	N	29051494
MGI:6358363	F	MP:0000627	abnormal mammary gland morphology	Mir31<em1Nju>/Mir31<em1Nju>	involves: C57BL/6J	N	29051494
MGI:6358363	F	MP:0000628	abnormal mammary gland development	Mir31<em1Nju>/Mir31<em1Nju>	involves: C57BL/6J	N	29051494
MGI:6358363	F	MP:0013782	abnormal mammary duct terminal end bud morphology	Mir31<em1Nju>/Mir31<em1Nju>	involves: C57BL/6J	N	29051494
MGI:6358363	F	MP:0004135	abnormal mammary gland embryonic development	Mir31<em1Nju>/Mir31<em1Nju>	involves: C57BL/6J	N	29051494
MGI:6358368	F	MP:0000628	abnormal mammary gland development	Mir31<tm1.1Smoc>/Mir31<tm1.1Smoc>,Tg(KRT14-cre)1Amc/0	involves: C57BL/6 * C57BL/6J * CBA	N	29051494
MGI:6358368	F	MP:0009506	abnormal mammary gland alveolus morphology	Mir31<tm1.1Smoc>/Mir31<tm1.1Smoc>,Tg(KRT14-cre)1Amc/0	involves: C57BL/6 * C57BL/6J * CBA	N	29051494
MGI:6358371	F	MP:0003447	decreased tumor growth/size	Mir31<em1Nju>/Mir31<em1Nju>,Tg(MMTV-PyVT)634Mul/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358371	F	MP:0010269	decreased mammary gland tumor incidence	Mir31<em1Nju>/Mir31<em1Nju>,Tg(MMTV-PyVT)634Mul/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358371	F	MP:0001661	extended life span	Mir31<em1Nju>/Mir31<em1Nju>,Tg(MMTV-PyVT)634Mul/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358371	F	MP:0001273	decreased metastatic potential	Mir31<em1Nju>/Mir31<em1Nju>,Tg(MMTV-PyVT)634Mul/0	involves: C57BL/6J * FVB/N	N	29051494
MGI:6358382	M	MP:0002675	asthenozoospermia	Clxn<tm1.1Osb>/Clxn<tm1.1Osb>	involves: C57BL * C57BL/6NSlc * DBA	N	31240264
MGI:6358406	F	MP:0005121	decreased circulating prolactin level	Mir205hg<tm1.1Oers>/Mir205hg<tm1.1Oers>	B6(Cg)-Mir205hg<tm1.1Oers>	N	30982661
MGI:6358413	F	MP:0005121	decreased circulating prolactin level	Mir205<tm1.1Mtm>/Mir205<tm1.1Mtm>	involves: 129P2/OlaHsd * C57BL/6	N	30982661
MGI:6358417	F	MP:0009012	short diestrus	Nsmf<tm1.2Mrkr>/Nsmf<tm1.2Mrkr>	involves: C57BL/6 * C57BL/6J	N	26977770
MGI:6358417	F	MP:0009020	prolonged metestrus	Nsmf<tm1.2Mrkr>/Nsmf<tm1.2Mrkr>	involves: C57BL/6 * C57BL/6J	N	26977770
MGI:6358417	F	MP:0031381	decreased secondary ovarian follicle number	Nsmf<tm1.2Mrkr>/Nsmf<tm1.2Mrkr>	involves: C57BL/6 * C57BL/6J	N	26977770
MGI:6358417	F	MP:0011129	decreased tertiary ovarian follicle number	Nsmf<tm1.2Mrkr>/Nsmf<tm1.2Mrkr>	involves: C57BL/6 * C57BL/6J	N	26977770
MGI:6358417	F	MP:0011125	decreased primary ovarian follicle number	Nsmf<tm1.2Mrkr>/Nsmf<tm1.2Mrkr>	involves: C57BL/6 * C57BL/6J	N	26977770
MGI:6358417	M	MP:0005379	endocrine/exocrine gland phenotype	Nsmf<tm1.2Mrkr>/Nsmf<tm1.2Mrkr>	involves: C57BL/6 * C57BL/6J	Y	26977770
MGI:6358417	F	MP:0005181	decreased circulating estradiol level	Nsmf<tm1.2Mrkr>/Nsmf<tm1.2Mrkr>	involves: C57BL/6 * C57BL/6J	N	26977770
MGI:6358553	M	MP:0005159	azoospermia	Zcwpw1<em1Kliu>/Zcwpw1<em1Kliu>	C57BL/6-Zcwpw1<em1Kliu>	N	31453335
MGI:6358553	F	MP:0001130	abnormal ovarian folliculogenesis	Zcwpw1<em1Kliu>/Zcwpw1<em1Kliu>	C57BL/6-Zcwpw1<em1Kliu>	N	31453335
MGI:6358553	F	MP:0001132	absent mature ovarian follicles	Zcwpw1<em1Kliu>/Zcwpw1<em1Kliu>	C57BL/6-Zcwpw1<em1Kliu>	N	31453335
MGI:6358553	F	MP:0002682	decreased mature ovarian follicle number	Zcwpw1<em1Kliu>/Zcwpw1<em1Kliu>	C57BL/6-Zcwpw1<em1Kliu>	N	31453335
MGI:6358553	M	MP:0001925	male infertility	Zcwpw1<em1Kliu>/Zcwpw1<em1Kliu>	C57BL/6-Zcwpw1<em1Kliu>	N	31453335
MGI:6358553	F	MP:0005168	abnormal female meiosis	Zcwpw1<em1Kliu>/Zcwpw1<em1Kliu>	C57BL/6-Zcwpw1<em1Kliu>	N	31453335
MGI:6358553	F	MP:0001926	female infertility	Zcwpw1<em1Kliu>/Zcwpw1<em1Kliu>	C57BL/6-Zcwpw1<em1Kliu>	N	31453335
MGI:6358553	M	MP:0009451	abnormal chromosomal synapsis	Zcwpw1<em1Kliu>/Zcwpw1<em1Kliu>	C57BL/6-Zcwpw1<em1Kliu>	N	31453335
MGI:6358553	F	MP:0004805	absent oocytes	Zcwpw1<em1Kliu>/Zcwpw1<em1Kliu>	C57BL/6-Zcwpw1<em1Kliu>	N	31453335
MGI:6358553	M	MP:0001156	abnormal spermatogenesis	Zcwpw1<em1Kliu>/Zcwpw1<em1Kliu>	C57BL/6-Zcwpw1<em1Kliu>	N	31453335
MGI:6358553	M	MP:0001147	small testis	Zcwpw1<em1Kliu>/Zcwpw1<em1Kliu>	C57BL/6-Zcwpw1<em1Kliu>	N	31453335
MGI:6358553	M	MP:0010948	abnormal double-strand DNA break repair	Zcwpw1<em1Kliu>/Zcwpw1<em1Kliu>	C57BL/6-Zcwpw1<em1Kliu>	N	31453335
MGI:6358553	M	MP:0008261	arrest of male meiosis	Zcwpw1<em1Kliu>/Zcwpw1<em1Kliu>	C57BL/6-Zcwpw1<em1Kliu>	N	31453335
MGI:6358633	M	MP:0008489	slow postnatal weight gain	Asap1<Gt(RRS873)Byg>/Asap1<Gt(RRS873)Byg>	FVB.129P2(B6)-Asap1<Gt(RRS873)Byg>	N	31246957
MGI:6358659	M	MP:0002216	abnormal seminiferous tubule morphology	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Nanos3<tm2(cre)Ysa>/Nanos3<+>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	28196692
MGI:6358659	M	MP:0006378	abnormal spermatogonia morphology	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Nanos3<tm2(cre)Ysa>/Nanos3<+>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	28196692
MGI:6358660	M	MP:0006378	abnormal spermatogonia morphology	Ctnnb1<tm1Mmt>/Ctnnb1<tm1Mmt>,Nanos3<tm2(cre)Ysa>/Nanos3<+>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	28196692
MGI:6358660	M	MP:0002216	abnormal seminiferous tubule morphology	Ctnnb1<tm1Mmt>/Ctnnb1<tm1Mmt>,Nanos3<tm2(cre)Ysa>/Nanos3<+>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	28196692
MGI:6358660	M	MP:0004852	decreased testis weight	Ctnnb1<tm1Mmt>/Ctnnb1<tm1Mmt>,Nanos3<tm2(cre)Ysa>/Nanos3<+>	involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	28196692
MGI:6358666	M	MP:0002216	abnormal seminiferous tubule morphology	Ctnnb1<tm2Kem>/Ctnnb1<tm2Kem>,Nanos3<tm2(cre)Ysa>/Nanos3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj	N	28196692
MGI:6358666	M	MP:0004852	decreased testis weight	Ctnnb1<tm2Kem>/Ctnnb1<tm2Kem>,Nanos3<tm2(cre)Ysa>/Nanos3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj	N	28196692
MGI:6358666	M	MP:0006378	abnormal spermatogonia morphology	Ctnnb1<tm2Kem>/Ctnnb1<tm2Kem>,Nanos3<tm2(cre)Ysa>/Nanos3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj	N	28196692
MGI:6358667	M	MP:0006378	abnormal spermatogonia morphology	Ctnnb1<tm2Kem>/Ctnnb1<+>,Nanos3<tm2(cre)Ysa>/Nanos3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj	N	28196692
MGI:6358667	M	MP:0002216	abnormal seminiferous tubule morphology	Ctnnb1<tm2Kem>/Ctnnb1<+>,Nanos3<tm2(cre)Ysa>/Nanos3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj	N	28196692
MGI:6358667	M	MP:0004852	decreased testis weight	Ctnnb1<tm2Kem>/Ctnnb1<+>,Nanos3<tm2(cre)Ysa>/Nanos3<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj	N	28196692
MGI:6358746	M	MP:0005578	teratozoospermia	Sun5<em1Wli>/Sun5<em1Wli>	involves: C57BL/6J * DBA/2	N	28945193
MGI:6358746	M	MP:0009838	abnormal sperm axoneme morphology	Sun5<em1Wli>/Sun5<em1Wli>	involves: C57BL/6J * DBA/2	N	28945193
MGI:6358746	M	MP:0009234	absent sperm head	Sun5<em1Wli>/Sun5<em1Wli>	involves: C57BL/6J * DBA/2	N	28945193
MGI:6358746	M	MP:0005389	reproductive system phenotype	Sun5<em1Wli>/Sun5<em1Wli>	involves: C57BL/6J * DBA/2	Y	28945193
MGI:6358746	M	MP:0001925	male infertility	Sun5<em1Wli>/Sun5<em1Wli>	involves: C57BL/6J * DBA/2	N	28945193
MGI:6358746	M	MP:0009230	abnormal sperm head morphology	Sun5<em1Wli>/Sun5<em1Wli>	involves: C57BL/6J * DBA/2	N	28945193
MGI:6358746	M	MP:0009830	abnormal sperm connecting piece morphology	Sun5<em1Wli>/Sun5<em1Wli>	involves: C57BL/6J * DBA/2	N	28945193
MGI:6358746	M	MP:0002686	globozoospermia	Sun5<em1Wli>/Sun5<em1Wli>	involves: C57BL/6J * DBA/2	N	28945193
MGI:6358746	M	MP:0004182	abnormal spermiation	Sun5<em1Wli>/Sun5<em1Wli>	involves: C57BL/6J * DBA/2	N	28945193
MGI:6358747	M	MP:0005389	reproductive system phenotype	Sun5<em1Wli>/Sun5<+>	involves: C57BL/6J * DBA/2	Y	28945193
MGI:6358779	M	MP:0014052	increased male germ cell apoptosis	Rnf216<tm1b(EUCOMM)Wtsi>/Rnf216<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	30649198
MGI:6358779	M	MP:0006380	abnormal spermatid morphology	Rnf216<tm1b(EUCOMM)Wtsi>/Rnf216<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	30649198
MGI:6358779	M	MP:0004901	decreased male germ cell number	Rnf216<tm1b(EUCOMM)Wtsi>/Rnf216<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	30649198
MGI:6358779	M	MP:0002631	abnormal epididymis morphology	Rnf216<tm1b(EUCOMM)Wtsi>/Rnf216<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	30649198
MGI:6358779	M	MP:0004852	decreased testis weight	Rnf216<tm1b(EUCOMM)Wtsi>/Rnf216<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	30649198
MGI:6358779	M	MP:0006379	abnormal spermatocyte morphology	Rnf216<tm1b(EUCOMM)Wtsi>/Rnf216<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	30649198
MGI:6358779	F	MP:0005389	reproductive system phenotype	Rnf216<tm1b(EUCOMM)Wtsi>/Rnf216<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	Y	30649198
MGI:6358779	M	MP:0001925	male infertility	Rnf216<tm1b(EUCOMM)Wtsi>/Rnf216<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	30649198
MGI:6358779	M	MP:0001147	small testis	Rnf216<tm1b(EUCOMM)Wtsi>/Rnf216<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	30649198
MGI:6358779	M	MP:0001156	abnormal spermatogenesis	Rnf216<tm1b(EUCOMM)Wtsi>/Rnf216<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	30649198
MGI:6358779	M	MP:0001154	seminiferous tubule degeneration	Rnf216<tm1b(EUCOMM)Wtsi>/Rnf216<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	30649198
MGI:6358806	M	MP:0006380	abnormal spermatid morphology	Sppl2c<tm1.1(KOMP)Vlcg>/Sppl2c<tm1.1(KOMP)Vlcg>	involves: C57BL/6NCrl * C57BL/6NTac	N	30733280
MGI:6358806	M	MP:0002675	asthenozoospermia	Sppl2c<tm1.1(KOMP)Vlcg>/Sppl2c<tm1.1(KOMP)Vlcg>	involves: C57BL/6NCrl * C57BL/6NTac	N	30733280
MGI:6358806	M	MP:0004852	decreased testis weight	Sppl2c<tm1.1(KOMP)Vlcg>/Sppl2c<tm1.1(KOMP)Vlcg>	involves: C57BL/6NCrl * C57BL/6NTac	N	30733280
MGI:6359429	M	MP:0001922	reduced male fertility	Pate4<tm1Osb>/Pate4<tm1Osb>	involves: C57BL/6 * C57BL/6NSlc * DBA/2	N	30452524
MGI:6359429	M	MP:0001935	decreased litter size	Pate4<tm1Osb>/Pate4<tm1Osb>	involves: C57BL/6 * C57BL/6NSlc * DBA/2	N	30452524
MGI:6359429	M	MP:0030982	abnormal copulatory plug deposition	Pate4<tm1Osb>/Pate4<tm1Osb>	involves: C57BL/6 * C57BL/6NSlc * DBA/2	N	30452524
MGI:6359429	M	MP:0002673	abnormal sperm number	Pate4<tm1Osb>/Pate4<tm1Osb>	involves: C57BL/6 * C57BL/6NSlc * DBA/2	N	30452524
MGI:6359430	M	MP:0005389	reproductive system phenotype	Cmtm1<em1Osb>/Cmtm1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	30209135
MGI:6359431	M	MP:0020869	immotile sperm	Cmtm2a<em1Osb>/Cmtm2a<em1Osb>,Cmtm2b<em1Osb>/Cmtm2b<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30209135
MGI:6359431	M	MP:0001925	male infertility	Cmtm2a<em1Osb>/Cmtm2a<em1Osb>,Cmtm2b<em1Osb>/Cmtm2b<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30209135
MGI:6359431	M	MP:0005389	reproductive system phenotype	Cmtm2a<em1Osb>/Cmtm2a<em1Osb>,Cmtm2b<em1Osb>/Cmtm2b<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	30209135
MGI:6359432	M	MP:0005389	reproductive system phenotype	Cmtm2a<em2Osb>/Cmtm2a<em2Osb>,Cmtm2b<em2Osb>/Cmtm2b<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	30209135
MGI:6359432	M	MP:0030978	impaired binding of sperm to zona pellucida	Cmtm2a<em2Osb>/Cmtm2a<em2Osb>,Cmtm2b<em2Osb>/Cmtm2b<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30209135
MGI:6359432	M	MP:0001922	reduced male fertility	Cmtm2a<em2Osb>/Cmtm2a<em2Osb>,Cmtm2b<em2Osb>/Cmtm2b<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30209135
MGI:6359434	M	MP:0001925	male infertility	Adam3<tm1Osb>/Adam3<tm1Osb>	involves: 129S2/SvPas * C57BL/6J * C57BL/6NSlc * DBA/2J	N	30209135
MGI:6359435	M	MP:0005389	reproductive system phenotype	Adam3<tm1Osb>/Adam3<tm1Osb>,Tg(Clgn-Adam3)1Osb/0	involves: 129S2/SvPas * C57BL/6J * C57BL/6NSlc * DBA/2J	Y	30209135
MGI:6359451	M	MP:0008489	slow postnatal weight gain	Fance<Tg(Tyr)2364E-2a2Ove>/Fance<Tg(Tyr)2364E-2a2Ove>	FVB/N-Fance<Tg(Tyr)2364E-2a2Ove>/Mmjax	N	27486799
MGI:6359451	M	MP:0002216	abnormal seminiferous tubule morphology	Fance<Tg(Tyr)2364E-2a2Ove>/Fance<Tg(Tyr)2364E-2a2Ove>	FVB/N-Fance<Tg(Tyr)2364E-2a2Ove>/Mmjax	N	27486799
MGI:6359451	M	MP:0001940	testis hypoplasia	Fance<Tg(Tyr)2364E-2a2Ove>/Fance<Tg(Tyr)2364E-2a2Ove>	FVB/N-Fance<Tg(Tyr)2364E-2a2Ove>/Mmjax	N	27486799
MGI:6359451	M	MP:0004901	decreased male germ cell number	Fance<Tg(Tyr)2364E-2a2Ove>/Fance<Tg(Tyr)2364E-2a2Ove>	FVB/N-Fance<Tg(Tyr)2364E-2a2Ove>/Mmjax	N	27486799
MGI:6359451	M	MP:0001922	reduced male fertility	Fance<Tg(Tyr)2364E-2a2Ove>/Fance<Tg(Tyr)2364E-2a2Ove>	FVB/N-Fance<Tg(Tyr)2364E-2a2Ove>/Mmjax	N	27486799
MGI:6359451	M	MP:0004852	decreased testis weight	Fance<Tg(Tyr)2364E-2a2Ove>/Fance<Tg(Tyr)2364E-2a2Ove>	FVB/N-Fance<Tg(Tyr)2364E-2a2Ove>/Mmjax	N	27486799
MGI:6359781	F	MP:0005179	decreased circulating cholesterol level	Cpgi5563<tm1.1(NCC)Wcs>/Cpgi5563<tm1.1(NCC)Wcs>	C57BL/6N-Cpgi5563<tm1.1(NCC)Wcs>/Wtsi	N	31354981
MGI:6359781	F	MP:0008347	decreased gamma-delta T cell number	Cpgi5563<tm1.1(NCC)Wcs>/Cpgi5563<tm1.1(NCC)Wcs>	C57BL/6N-Cpgi5563<tm1.1(NCC)Wcs>/Wtsi	N	31354981
MGI:6359847	M	MP:0014464	decreased sperm mitochondrial sheath size	Gykl1<em#Juhu>/Gykl1<em#Juhu>	C57BL/6J-Gykl1<em#Juhu>	N	28852571
MGI:6359847	M	MP:0002674	abnormal sperm motility	Gykl1<em#Juhu>/Gykl1<em#Juhu>	C57BL/6J-Gykl1<em#Juhu>	N	28852571
MGI:6359847	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Gykl1<em#Juhu>/Gykl1<em#Juhu>	C57BL/6J-Gykl1<em#Juhu>	N	28852571
MGI:6359847	M	MP:0002687	oligozoospermia	Gykl1<em#Juhu>/Gykl1<em#Juhu>	C57BL/6J-Gykl1<em#Juhu>	N	28852571
MGI:6359847	M	MP:0001925	male infertility	Gykl1<em#Juhu>/Gykl1<em#Juhu>	C57BL/6J-Gykl1<em#Juhu>	N	28852571
MGI:6359847	M	MP:0008892	abnormal sperm flagellum morphology	Gykl1<em#Juhu>/Gykl1<em#Juhu>	C57BL/6J-Gykl1<em#Juhu>	N	28852571
MGI:6359847	M	MP:0005389	reproductive system phenotype	Gykl1<em#Juhu>/Gykl1<em#Juhu>	C57BL/6J-Gykl1<em#Juhu>	Y	28852571
MGI:6359847	M	MP:0009237	kinked sperm flagellum	Gykl1<em#Juhu>/Gykl1<em#Juhu>	C57BL/6J-Gykl1<em#Juhu>	N	28852571
MGI:6359848	M	MP:0001922	reduced male fertility	Gykl1<em#Juhu>/Gykl1<+>	C57BL/6J-Gykl1<em#Juhu>	N	28852571
MGI:6359848	M	MP:0009237	kinked sperm flagellum	Gykl1<em#Juhu>/Gykl1<+>	C57BL/6J-Gykl1<em#Juhu>	N	28852571
MGI:6359848	M	MP:0002674	abnormal sperm motility	Gykl1<em#Juhu>/Gykl1<+>	C57BL/6J-Gykl1<em#Juhu>	N	28852571
MGI:6359848	M	MP:0014464	decreased sperm mitochondrial sheath size	Gykl1<em#Juhu>/Gykl1<+>	C57BL/6J-Gykl1<em#Juhu>	N	28852571
MGI:6359850	M	MP:0005389	reproductive system phenotype	Gk2<em#Juhu>/Gk2<em#Juhu>	C57BL/6J-Gk2<em#Juhu>	Y	28852571
MGI:6359850	M	MP:0009831	abnormal sperm midpiece morphology	Gk2<em#Juhu>/Gk2<em#Juhu>	C57BL/6J-Gk2<em#Juhu>	N	28852571
MGI:6359850	M	MP:0002687	oligozoospermia	Gk2<em#Juhu>/Gk2<em#Juhu>	C57BL/6J-Gk2<em#Juhu>	N	28852571
MGI:6359850	M	MP:0014464	decreased sperm mitochondrial sheath size	Gk2<em#Juhu>/Gk2<em#Juhu>	C57BL/6J-Gk2<em#Juhu>	N	28852571
MGI:6359850	M	MP:0009237	kinked sperm flagellum	Gk2<em#Juhu>/Gk2<em#Juhu>	C57BL/6J-Gk2<em#Juhu>	N	28852571
MGI:6359850	M	MP:0002674	abnormal sperm motility	Gk2<em#Juhu>/Gk2<em#Juhu>	C57BL/6J-Gk2<em#Juhu>	N	28852571
MGI:6359850	M	MP:0001925	male infertility	Gk2<em#Juhu>/Gk2<em#Juhu>	C57BL/6J-Gk2<em#Juhu>	N	28852571
MGI:6359850	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Gk2<em#Juhu>/Gk2<em#Juhu>	C57BL/6J-Gk2<em#Juhu>	N	28852571
MGI:6359852	M	MP:0002674	abnormal sperm motility	Gk2<em#Juhu>/Gk2<+>	C57BL/6J-Gk2<em#Juhu>	N	28852571
MGI:6359852	M	MP:0005389	reproductive system phenotype	Gk2<em#Juhu>/Gk2<+>	C57BL/6J-Gk2<em#Juhu>	Y	28852571
MGI:6359852	M	MP:0014464	decreased sperm mitochondrial sheath size	Gk2<em#Juhu>/Gk2<+>	C57BL/6J-Gk2<em#Juhu>	N	28852571
MGI:6359852	M	MP:0009237	kinked sperm flagellum	Gk2<em#Juhu>/Gk2<+>	C57BL/6J-Gk2<em#Juhu>	N	28852571
MGI:6359879	F	MP:0005389	reproductive system phenotype	Gk2<em1Osb>/Gk2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	30662012
MGI:6359879	M	MP:0000242	impaired fertilization	Gk2<em1Osb>/Gk2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30662012
MGI:6359879	M	MP:0002675	asthenozoospermia	Gk2<em1Osb>/Gk2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30662012
MGI:6359879	M	MP:0001925	male infertility	Gk2<em1Osb>/Gk2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30662012
MGI:6359879	M	MP:0009237	kinked sperm flagellum	Gk2<em1Osb>/Gk2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30662012
MGI:6359879	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Gk2<em1Osb>/Gk2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30662012
MGI:6359880	M	MP:0000242	impaired fertilization	Gk2<em1Osb>/Gk2<em1Osb>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: C57BL/6NJcl * DBA/2NJcl	N	30662012
MGI:6360262	F	MP:0005473	decreased triiodothyronine level	4931414P19Rik<em1Lych>/4931414P19Rik<em1Lych>	involves: C57BL/6	N	28230092
MGI:6360262	F	MP:0003503	decreased activity of thyroid gland	4931414P19Rik<em1Lych>/4931414P19Rik<em1Lych>	involves: C57BL/6	N	28230092
MGI:6360262	F	MP:0005122	increased circulating thyroid-stimulating hormone level	4931414P19Rik<em1Lych>/4931414P19Rik<em1Lych>	involves: C57BL/6	N	28230092
MGI:6360262	F	MP:0005471	decreased thyroxine level	4931414P19Rik<em1Lych>/4931414P19Rik<em1Lych>	involves: C57BL/6	N	28230092
MGI:6360458	M	MP:0004852	decreased testis weight	Ndrg3<em1Qshi>/Ndrg3<+>	C57BL/6-Ndrg3<em1Qshi>	N	28290521
MGI:6360458	M	MP:0010948	abnormal double-strand DNA break repair	Ndrg3<em1Qshi>/Ndrg3<+>	C57BL/6-Ndrg3<em1Qshi>	N	28290521
MGI:6360458	M	MP:0005169	abnormal male meiosis	Ndrg3<em1Qshi>/Ndrg3<+>	C57BL/6-Ndrg3<em1Qshi>	N	28290521
MGI:6360458	M	MP:0001922	reduced male fertility	Ndrg3<em1Qshi>/Ndrg3<+>	C57BL/6-Ndrg3<em1Qshi>	N	28290521
MGI:6360458	M	MP:0002687	oligozoospermia	Ndrg3<em1Qshi>/Ndrg3<+>	C57BL/6-Ndrg3<em1Qshi>	N	28290521
MGI:6360617	M	MP:0006378	abnormal spermatogonia morphology	H3f4<em1Osb>/H3f4<em1Osb>	involves: C57BL/6	N	28099840
MGI:6360617	M	MP:0014052	increased male germ cell apoptosis	H3f4<em1Osb>/H3f4<em1Osb>	involves: C57BL/6	N	28099840
MGI:6360617	M	MP:0001156	abnormal spermatogenesis	H3f4<em1Osb>/H3f4<em1Osb>	involves: C57BL/6	N	28099840
MGI:6360617	M	MP:0006380	abnormal spermatid morphology	H3f4<em1Osb>/H3f4<em1Osb>	involves: C57BL/6	N	28099840
MGI:6360617	M	MP:0005159	azoospermia	H3f4<em1Osb>/H3f4<em1Osb>	involves: C57BL/6	N	28099840
MGI:6360617	M	MP:0002662	abnormal cauda epididymis morphology	H3f4<em1Osb>/H3f4<em1Osb>	involves: C57BL/6	N	28099840
MGI:6360617	M	MP:0001925	male infertility	H3f4<em1Osb>/H3f4<em1Osb>	involves: C57BL/6	N	28099840
MGI:6360617	M	MP:0005169	abnormal male meiosis	H3f4<em1Osb>/H3f4<em1Osb>	involves: C57BL/6	N	28099840
MGI:6360617	M	MP:0004901	decreased male germ cell number	H3f4<em1Osb>/H3f4<em1Osb>	involves: C57BL/6	N	28099840
MGI:6360617	M	MP:0006379	abnormal spermatocyte morphology	H3f4<em1Osb>/H3f4<em1Osb>	involves: C57BL/6	N	28099840
MGI:6360617	F	MP:0005389	reproductive system phenotype	H3f4<em1Osb>/H3f4<em1Osb>	involves: C57BL/6	Y	28099840
MGI:6360617	M	MP:0001147	small testis	H3f4<em1Osb>/H3f4<em1Osb>	involves: C57BL/6	N	28099840
MGI:6360703	M	MP:0005159	azoospermia	Odad3<tm1b(EUCOMM)Hmgu>/Odad3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Odad3<tm1b(EUCOMM)Hmgu>/Cnrm	N	31383820
MGI:6360704	M	MP:0002687	oligozoospermia	Odad3<tm1c(EUCOMM)Hmgu>/Odad3<tm1c(EUCOMM)Hmgu>,Gt(ROSA)26Sor<tm2(cre/ERT2)Brn>/Gt(ROSA)26Sor<+>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6N	N	31383820
MGI:6360704	M	MP:0002675	asthenozoospermia	Odad3<tm1c(EUCOMM)Hmgu>/Odad3<tm1c(EUCOMM)Hmgu>,Gt(ROSA)26Sor<tm2(cre/ERT2)Brn>/Gt(ROSA)26Sor<+>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6N	N	31383820
MGI:6360860	F	MP:0010025	decreased total body fat amount	Slc2a6<em1Rbr>/Slc2a6<em1Rbr>	C57BL/6J-Slc2a6<em1Rbr>	N	29664675
MGI:6360860	F	MP:0010379	decreased respiratory quotient	Slc2a6<em1Rbr>/Slc2a6<em1Rbr>	C57BL/6J-Slc2a6<em1Rbr>	N	29664675
MGI:6360937	M	MP:0001364	decreased anxiety-related response	St3gal5<tm1Rlp>/St3gal5<tm1Rlp>	involves: C57BL/6JJmsSlc	N	21333627
MGI:6360937	M	MP:0010698	abnormal impulsive behavior control	St3gal5<tm1Rlp>/St3gal5<tm1Rlp>	involves: C57BL/6JJmsSlc	N	21333627
MGI:6360937	M	MP:0014114	abnormal cognition	St3gal5<tm1Rlp>/St3gal5<tm1Rlp>	involves: C57BL/6JJmsSlc	N	21333627
MGI:6360960	M	MP:0009647	decreased fertilization frequency	Spata46<tm1Itl>/Spata46<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6NTac	N	27488028
MGI:6360960	M	MP:0006380	abnormal spermatid morphology	Spata46<tm1Itl>/Spata46<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6NTac	N	27488028
MGI:6360960	M	MP:0030980	abnormal acroplaxome morphology	Spata46<tm1Itl>/Spata46<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6NTac	N	27488028
MGI:6360960	M	MP:0001932	abnormal spermiogenesis	Spata46<tm1Itl>/Spata46<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6NTac	N	27488028
MGI:6360960	M	MP:0000242	impaired fertilization	Spata46<tm1Itl>/Spata46<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6NTac	N	27488028
MGI:6360960	M	MP:0005578	teratozoospermia	Spata46<tm1Itl>/Spata46<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6NTac	N	27488028
MGI:6360960	M	MP:0009230	abnormal sperm head morphology	Spata46<tm1Itl>/Spata46<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6NTac	N	27488028
MGI:6360960	M	MP:0009232	abnormal sperm nucleus morphology	Spata46<tm1Itl>/Spata46<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6NTac	N	27488028
MGI:6360960	M	MP:0001922	reduced male fertility	Spata46<tm1Itl>/Spata46<tm1Itl>	involves: 129S6/SvEvTac * C57BL/6NTac	N	27488028
MGI:6361090	F	MP:0001125	abnormal oocyte morphology	Chd9<em1Ibbr>/Chd9<em1Ibbr>	C57BL/6N-Chd9<em1Ibbr>	N	29665362
MGI:6361090	F	MP:0005389	reproductive system phenotype	Chd9<em1Ibbr>/Chd9<em1Ibbr>	C57BL/6N-Chd9<em1Ibbr>	Y	29665362
MGI:6361091	F	MP:0001125	abnormal oocyte morphology	Chd9<em2Ibbr>/Chd9<em2Ibbr>	C57BL/6N-Chd9<em2Ibbr>	N	29665362
MGI:6361091	F	MP:0005389	reproductive system phenotype	Chd9<em2Ibbr>/Chd9<em2Ibbr>	C57BL/6N-Chd9<em2Ibbr>	Y	29665362
MGI:6361092	M	MP:0001262	decreased body weight	Or4m1<em1Tshu>/Or4m1<em1Tshu>	involves: C57BL/6J	N	31798959
MGI:6361092	M	MP:0000188	abnormal circulating glucose level	Or4m1<em1Tshu>/Or4m1<em1Tshu>	involves: C57BL/6J	N	31798959
MGI:6361092	M	MP:0005378	growth/size/body region phenotype	Or4m1<em1Tshu>/Or4m1<em1Tshu>	involves: C57BL/6J	Y	31798959
MGI:6361092	M	MP:0001922	reduced male fertility	Or4m1<em1Tshu>/Or4m1<em1Tshu>	involves: C57BL/6J	N	31798959
MGI:6361092	M	MP:0009647	decreased fertilization frequency	Or4m1<em1Tshu>/Or4m1<em1Tshu>	involves: C57BL/6J	N	31798959
MGI:6361092	M	MP:0002675	asthenozoospermia	Or4m1<em1Tshu>/Or4m1<em1Tshu>	involves: C57BL/6J	N	31798959
MGI:6361092	M	MP:0004543	abnormal sperm physiology	Or4m1<em1Tshu>/Or4m1<em1Tshu>	involves: C57BL/6J	N	31798959
MGI:6361092	M	MP:0020451	decreased sperm progressive motility	Or4m1<em1Tshu>/Or4m1<em1Tshu>	involves: C57BL/6J	N	31798959
MGI:6361092	M	MP:0005659	decreased susceptibility to diet-induced obesity	Or4m1<em1Tshu>/Or4m1<em1Tshu>	involves: C57BL/6J	N	31798959
MGI:6361092	M	MP:0005376	homeostasis/metabolism phenotype	Or4m1<em1Tshu>/Or4m1<em1Tshu>	involves: C57BL/6J	Y	31798959
MGI:6361092	M	MP:0005389	reproductive system phenotype	Or4m1<em1Tshu>/Or4m1<em1Tshu>	involves: C57BL/6J	Y	31798959
MGI:6361119	M	MP:0005389	reproductive system phenotype	Pate1<em1Osb>/Pate1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	30927342
MGI:6361120	M	MP:0005389	reproductive system phenotype	Pate2<em1Osb>/Pate2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	30927342
MGI:6361121	M	MP:0005389	reproductive system phenotype	Pate3<em1Osb>/Pate3<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	30927342
MGI:6361122	M	MP:0005389	reproductive system phenotype	Clpsl2<em1Osb>/Clpsl2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	30927342
MGI:6361123	M	MP:0005389	reproductive system phenotype	Del(9Glb1l2-Gm1110)1Osb/Del(9Glb1l2-Gm1110)1Osb	involves: C57BL/6J * DBA/2J	Y	30927342
MGI:6361124	M	MP:0005389	reproductive system phenotype	Eddm13<em1Osb>/Eddm13<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	30927342
MGI:6361125	M	MP:0005389	reproductive system phenotype	Rnase13<em1Osb>/Rnase13<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	30927342
MGI:6361134	M	MP:0005389	reproductive system phenotype	Trim17<em1Osb>/Trim17<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361137	M	MP:0005389	reproductive system phenotype	Mgat4d<em1Osb>/Mgat4d<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361210	M	MP:0031012	impaired sperm migration in female genital tract	Pgap1<tm1Osb>/Pgap1<tm1Osb>	involves: 129S2/SvPas	N	17711852
MGI:6361210	M	MP:0001925	male infertility	Pgap1<tm1Osb>/Pgap1<tm1Osb>	involves: 129S2/SvPas	N	17711852
MGI:6361210	M	MP:0030978	impaired binding of sperm to zona pellucida	Pgap1<tm1Osb>/Pgap1<tm1Osb>	involves: 129S2/SvPas	N	17711852
MGI:6361210	M	MP:0000242	impaired fertilization	Pgap1<tm1Osb>/Pgap1<tm1Osb>	involves: 129S2/SvPas	N	17711852
MGI:6361298	M	MP:0005389	reproductive system phenotype	Cwh43<em1Osb>/Cwh43<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361299	M	MP:0005389	reproductive system phenotype	X/Kdm5d<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361301	M	MP:0005389	reproductive system phenotype	Nudt10<em1Osb>/Y	involves: C57BL/6J * C57BL/6NSlc * DBA/2J	Y	31201419
MGI:6361302	M	MP:0005389	reproductive system phenotype	Tmem19<em1Osb>/Tmem19<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361316	M	MP:0005389	reproductive system phenotype	1700001O22Rik<em1Osb>/1700001O22Rik<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361317	M	MP:0005389	reproductive system phenotype	1700010B08Rik<em1Osb>/1700010B08Rik<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361318	M	MP:0005389	reproductive system phenotype	Ankrd7<em1Osb>/Ankrd7<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361319	M	MP:0005389	reproductive system phenotype	Banf2<em1Osb>/Banf2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361320	M	MP:0005389	reproductive system phenotype	Bpifa3<em1Osb>/Bpifa3<em1Osb>	involves: C57BL/6J * C57BL/6NSlc * DBA/2J	Y	31201419
MGI:6361321	M	MP:0005389	reproductive system phenotype	Cct6b<em1Osb>/Cct6b<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361322	M	MP:0005389	reproductive system phenotype	Fam221b<em1Osb>/Fam221b<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361323	M	MP:0005389	reproductive system phenotype	Fam221b<em1Osb>/Fam221b<em3Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361324	M	MP:0005389	reproductive system phenotype	Fndc8<em1Osb>/Fndc8<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361325	M	MP:0005389	reproductive system phenotype	Gsg1<em1Osb>/Gsg1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361326	M	MP:0005389	reproductive system phenotype	Hmgb4<em1Osb>/Hmgb4<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361327	M	MP:0005389	reproductive system phenotype	Hyal6<em1Osb>/Hyal6<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361328	M	MP:0005389	reproductive system phenotype	Morn3<em1Osb>/Morn3<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361329	M	MP:0005389	reproductive system phenotype	Oxct2a<em1Osb>/Oxct2a<em1Osb>,Oxct2b<em1Osb>/Oxct2b<em1Osb>	involves: C57BL/6J * C57BL/6NSlc * DBA/2J	Y	31201419
MGI:6361330	M	MP:0005389	reproductive system phenotype	Scp2d1<em1Osb>/Scp2d1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361332	M	MP:0005389	reproductive system phenotype	Slc36a3<em1Osb>/Slc36a3<em1Osb>	involves: C57BL/6J * C57BL/6NSlc * DBA/2J	Y	31201419
MGI:6361333	M	MP:0005389	reproductive system phenotype	Tex13a<em1Osb>/Y	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361334	M	MP:0005389	reproductive system phenotype	Tex13b<em1Osb>/Y	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361335	M	MP:0005389	reproductive system phenotype	Tex35<em1Osb>/Tex35<em1Osb>	involves: C57BL/6J * C57BL/6NSlc * DBA/2J	Y	31201419
MGI:6361338	M	MP:0005389	reproductive system phenotype	Tgif2lx1<em1Osb>/Y	involves: C57BL/6J * C57BL/6NSlc * DBA/2J	Y	31201419
MGI:6361340	M	MP:0005389	reproductive system phenotype	Tktl2<em1Osb>/Tktl2<em1Osb>	involves: C57BL/6J * C57BL/6NSlc * DBA/2J	Y	31201419
MGI:6361342	M	MP:0005389	reproductive system phenotype	Tmem202<em1Osb>/Tmem202<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361343	M	MP:0005389	reproductive system phenotype	Tmem202<em1Osb>/Tmem202<em3Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361344	M	MP:0005389	reproductive system phenotype	Tmem270<em1Osb>/Tmem270<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361345	M	MP:0005389	reproductive system phenotype	Trpd52l3<em1Osb>/Trpd52l3<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361346	M	MP:0005389	reproductive system phenotype	Ube2d2b<em1Osb>/Ube2d2b<em1Osb>	involves: C57BL/6J * C57BL/6NSlc * DBA/2J	Y	31201419
MGI:6361347	M	MP:0005389	reproductive system phenotype	Ubqln5<em1Osb>/Ubqln5<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361348	M	MP:0005389	reproductive system phenotype	Usp26<em1Osb>/Y	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361349	M	MP:0005389	reproductive system phenotype	Vwa3b<em1Osb>/Vwa3b<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	31201419
MGI:6361418	M	MP:0009232	abnormal sperm nucleus morphology	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0001932	abnormal spermiogenesis	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0005578	teratozoospermia	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0002687	oligozoospermia	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0002784	abnormal Sertoli cell morphology	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0006380	abnormal spermatid morphology	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0001925	male infertility	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0031354	abnormal acrosome assembly	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0009831	abnormal sperm midpiece morphology	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0009230	abnormal sperm head morphology	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0008545	absent sperm flagellum	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0020869	immotile sperm	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0009838	abnormal sperm axoneme morphology	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0004182	abnormal spermiation	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0009239	short sperm flagellum	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0030942	abnormal microtubule organizing center morphology	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361418	M	MP:0008892	abnormal sperm flagellum morphology	Cetn1<tm1.1Wbae>/Cetn1<tm1.1Wbae>	Not Specified	N	23641067
MGI:6361428	M	MP:0005389	reproductive system phenotype	Prss54<em1Bcm>/Prss54<em1Bcm>	involves: 129 * C57BL/6J * DBA/2J	Y	31403672
MGI:6361429	M	MP:0005389	reproductive system phenotype	Prss44<em1Osb>/Prss44<em1Osb>	involves: C57BL/6NSlc	Y	31403672
MGI:6361430	M	MP:0005389	reproductive system phenotype	Prss46<em1Osb>/Prss46<em1Osb>	involves: C57BL/6NSlc	Y	31403672
MGI:6361590	M	MP:0004543	abnormal sperm physiology	Ttll9<tm1Seto>/Ttll9<tm1Seto>	involves: C57BL/6N	N	27257088
MGI:6361590	M	MP:0009838	abnormal sperm axoneme morphology	Ttll9<tm1Seto>/Ttll9<tm1Seto>	involves: C57BL/6N	N	27257088
MGI:6361590	M	MP:0001925	male infertility	Ttll9<tm1Seto>/Ttll9<tm1Seto>	involves: C57BL/6N	N	27257088
MGI:6361590	M	MP:0005578	teratozoospermia	Ttll9<tm1Seto>/Ttll9<tm1Seto>	involves: C57BL/6N	N	27257088
MGI:6361590	M	MP:0002675	asthenozoospermia	Ttll9<tm1Seto>/Ttll9<tm1Seto>	involves: C57BL/6N	N	27257088
MGI:6361590	M	MP:0008893	detached sperm flagellum	Ttll9<tm1Seto>/Ttll9<tm1Seto>	involves: C57BL/6N	N	27257088
MGI:6361590	M	MP:0004884	abnormal testis physiology	Ttll9<tm1Seto>/Ttll9<tm1Seto>	involves: C57BL/6N	N	27257088
MGI:6361590	M	MP:0009836	abnormal sperm principal piece morphology	Ttll9<tm1Seto>/Ttll9<tm1Seto>	involves: C57BL/6N	N	27257088
MGI:6361590	M	MP:0020451	decreased sperm progressive motility	Ttll9<tm1Seto>/Ttll9<tm1Seto>	involves: C57BL/6N	N	27257088
MGI:6361590	M	MP:0030590	abnormal sperm fibrous sheath morphology	Ttll9<tm1Seto>/Ttll9<tm1Seto>	involves: C57BL/6N	N	27257088
MGI:6361590	M	MP:0002687	oligozoospermia	Ttll9<tm1Seto>/Ttll9<tm1Seto>	involves: C57BL/6N	N	27257088
MGI:6361865	M	MP:0003020	decreased circulating chloride level	Pdgfd<tm1Ueks>/Pdgfd<tm1Ueks>	B6.Cg-Pdgfd<tm1Ueks>	N	27032083
MGI:6361865	M	MP:0000194	increased circulating calcium level	Pdgfd<tm1Ueks>/Pdgfd<tm1Ueks>	B6.Cg-Pdgfd<tm1Ueks>	N	27032083
MGI:6362620	F	MP:0002169	no abnormal phenotype detected	Scml1<tm1.2Atot>/Scml1<tm1.2Atot>	STOCK Scml1<tm1.2Atot>/Atot	N	27165042
MGI:6362621	M	MP:0005389	reproductive system phenotype	Scml1<tm1.2Atot>/Y	STOCK Scml1<tm1.2Atot>/Atot	Y	27165042
MGI:6362621	M	MP:0006379	abnormal spermatocyte morphology	Scml1<tm1.2Atot>/Y	STOCK Scml1<tm1.2Atot>/Atot	N	27165042
MGI:6362718	M	MP:0001262	decreased body weight	Golga2<tm1(KOMP)Vlcg>/Golga2<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	29128360
MGI:6363007	M	MP:0008261	arrest of male meiosis	Terb2<em1Leim>/Terb2<em1Leim>	C57BL/6-Terb2<em1Leim>	N	30718482
MGI:6363007	F	MP:0001926	female infertility	Terb2<em1Leim>/Terb2<em1Leim>	C57BL/6-Terb2<em1Leim>	N	30718482
MGI:6363007	M	MP:0014052	increased male germ cell apoptosis	Terb2<em1Leim>/Terb2<em1Leim>	C57BL/6-Terb2<em1Leim>	N	30718482
MGI:6363007	F	MP:0004856	decreased ovary weight	Terb2<em1Leim>/Terb2<em1Leim>	C57BL/6-Terb2<em1Leim>	N	30718482
MGI:6363007	M	MP:0001147	small testis	Terb2<em1Leim>/Terb2<em1Leim>	C57BL/6-Terb2<em1Leim>	N	30718482
MGI:6363007	F	MP:0001127	small ovary	Terb2<em1Leim>/Terb2<em1Leim>	C57BL/6-Terb2<em1Leim>	N	30718482
MGI:6363007	M	MP:0004852	decreased testis weight	Terb2<em1Leim>/Terb2<em1Leim>	C57BL/6-Terb2<em1Leim>	N	30718482
MGI:6363007	M	MP:0010948	abnormal double-strand DNA break repair	Terb2<em1Leim>/Terb2<em1Leim>	C57BL/6-Terb2<em1Leim>	N	30718482
MGI:6363007	M	MP:0001925	male infertility	Terb2<em1Leim>/Terb2<em1Leim>	C57BL/6-Terb2<em1Leim>	N	30718482
MGI:6363007	M	MP:0005159	azoospermia	Terb2<em1Leim>/Terb2<em1Leim>	C57BL/6-Terb2<em1Leim>	N	30718482
MGI:6363007	F	MP:0002777	absent ovarian follicles	Terb2<em1Leim>/Terb2<em1Leim>	C57BL/6-Terb2<em1Leim>	N	30718482
MGI:6363007	F	MP:0005168	abnormal female meiosis	Terb2<em1Leim>/Terb2<em1Leim>	C57BL/6-Terb2<em1Leim>	N	30718482
MGI:6363007	F	MP:0009452	abnormal synaptonemal complex	Terb2<em1Leim>/Terb2<em1Leim>	C57BL/6-Terb2<em1Leim>	N	30718482
MGI:6363009	F	MP:0009452	abnormal synaptonemal complex	Terb2<em2Leim>/Terb2<em2Leim>	C57BL/6-Terb2<em2Leim>	N	30718482
MGI:6363009	M	MP:0005159	azoospermia	Terb2<em2Leim>/Terb2<em2Leim>	C57BL/6-Terb2<em2Leim>	N	30718482
MGI:6363009	F	MP:0001127	small ovary	Terb2<em2Leim>/Terb2<em2Leim>	C57BL/6-Terb2<em2Leim>	N	30718482
MGI:6363009	F	MP:0005168	abnormal female meiosis	Terb2<em2Leim>/Terb2<em2Leim>	C57BL/6-Terb2<em2Leim>	N	30718482
MGI:6363009	M	MP:0008261	arrest of male meiosis	Terb2<em2Leim>/Terb2<em2Leim>	C57BL/6-Terb2<em2Leim>	N	30718482
MGI:6363009	F	MP:0001926	female infertility	Terb2<em2Leim>/Terb2<em2Leim>	C57BL/6-Terb2<em2Leim>	N	30718482
MGI:6363009	F	MP:0004856	decreased ovary weight	Terb2<em2Leim>/Terb2<em2Leim>	C57BL/6-Terb2<em2Leim>	N	30718482
MGI:6363009	M	MP:0014052	increased male germ cell apoptosis	Terb2<em2Leim>/Terb2<em2Leim>	C57BL/6-Terb2<em2Leim>	N	30718482
MGI:6363009	M	MP:0001147	small testis	Terb2<em2Leim>/Terb2<em2Leim>	C57BL/6-Terb2<em2Leim>	N	30718482
MGI:6363009	M	MP:0010948	abnormal double-strand DNA break repair	Terb2<em2Leim>/Terb2<em2Leim>	C57BL/6-Terb2<em2Leim>	N	30718482
MGI:6363009	M	MP:0001925	male infertility	Terb2<em2Leim>/Terb2<em2Leim>	C57BL/6-Terb2<em2Leim>	N	30718482
MGI:6363009	M	MP:0004852	decreased testis weight	Terb2<em2Leim>/Terb2<em2Leim>	C57BL/6-Terb2<em2Leim>	N	30718482
MGI:6363009	F	MP:0002777	absent ovarian follicles	Terb2<em2Leim>/Terb2<em2Leim>	C57BL/6-Terb2<em2Leim>	N	30718482
MGI:6363011	M	MP:0030024	abnormal meiotic attachment of telomere to nuclear envelope	Sun1<em1Leim>/Sun1<em1Leim>	C57BL/6-Sun1<em1Leim>	N	30718482
MGI:6363164	M	MP:0020414	abnormal fibroblast physiology	Usp11<tm1Tac>/Y	involves: 129 * C57BL/6	N	30733438
MGI:6363164	M	MP:0011703	increased fibroblast proliferation	Usp11<tm1Tac>/Y	involves: 129 * C57BL/6	N	30733438
MGI:6363164	M	MP:0001167	prostate gland epithelial hyperplasia	Usp11<tm1Tac>/Y	involves: 129 * C57BL/6	N	30733438
MGI:6363164	M	MP:0004958	enlarged prostate gland	Usp11<tm1Tac>/Y	involves: 129 * C57BL/6	N	30733438
MGI:6363165	F	MP:0010768	mortality/aging	Usp11<tm1Tac>/Usp11<tm1Tac>	involves: 129 * C57BL/6	Y	30733438
MGI:6363166	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Tg(TRAMP)8247Ng/0,Usp11<tm1Tac>/Y	involves: 129 * C57BL/6	N	30733438
MGI:6363166	M	MP:0001272	increased metastatic potential	Tg(TRAMP)8247Ng/0,Usp11<tm1Tac>/Y	involves: 129 * C57BL/6	N	30733438
MGI:6363166	M	MP:0003721	increased tumor growth/size	Tg(TRAMP)8247Ng/0,Usp11<tm1Tac>/Y	involves: 129 * C57BL/6	N	30733438
MGI:6363166	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Tg(TRAMP)8247Ng/0,Usp11<tm1Tac>/Y	involves: 129 * C57BL/6	N	30733438
MGI:6363217	M	MP:0005129	increased adrenocorticotropin level	Mrap<tm1.2Geno>/Mrap<tm1.2Geno>	involves: C57BL/6	N	29879378
MGI:6363217	M	MP:0002665	decreased circulating corticosterone level	Mrap<tm1.2Geno>/Mrap<tm1.2Geno>	involves: C57BL/6	N	29879378
MGI:6363243	M	MP:0002803	abnormal operant conditioning behavior	Gprin3<em1Sns>/Gprin3<em1Sns>	C57BL/6-Gprin3<em1Sns>	N	31363062
MGI:6363243	M	MP:0009758	impaired behavioral response to cocaine	Gprin3<em1Sns>/Gprin3<em1Sns>	C57BL/6-Gprin3<em1Sns>	N	31363062
MGI:6363243	M	MP:0002272	abnormal nervous system electrophysiology	Gprin3<em1Sns>/Gprin3<em1Sns>	C57BL/6-Gprin3<em1Sns>	N	31363062
MGI:6363243	M	MP:0008143	abnormal dendrite morphology	Gprin3<em1Sns>/Gprin3<em1Sns>	C57BL/6-Gprin3<em1Sns>	N	31363062
MGI:6363243	M	MP:0008462	abnormal medium spiny neuron morphology	Gprin3<em1Sns>/Gprin3<em1Sns>	C57BL/6-Gprin3<em1Sns>	N	31363062
MGI:6363245	M	MP:0008143	abnormal dendrite morphology	Gprin3<em1Sns>/Gprin3<em1Sns>,Tg(Drd2-EGFP)S118Gsat/0	involves: C57BL/6 * C57BL/6J * CD-1 * FVB/NTac	N	31363062
MGI:6363245	M	MP:0002272	abnormal nervous system electrophysiology	Gprin3<em1Sns>/Gprin3<em1Sns>,Tg(Drd2-EGFP)S118Gsat/0	involves: C57BL/6 * C57BL/6J * CD-1 * FVB/NTac	N	31363062
MGI:6364809	M	MP:0008489	slow postnatal weight gain	Arhgap17<Gt(RRN062)Byg>/Arhgap17<Gt(RRN062)Byg>	B6.129P2-Arhgap17<Gt(RRN062)Byg>	N	27229483
MGI:6364867	M	MP:0004543	abnormal sperm physiology	Psma8<em1Yuc>/Psma8<em1Yuc>	C57BL/6-Psma8<em1Yuc>	N	31358751
MGI:6364867	M	MP:0006380	abnormal spermatid morphology	Psma8<em1Yuc>/Psma8<em1Yuc>	C57BL/6-Psma8<em1Yuc>	N	31358751
MGI:6364867	M	MP:0005159	azoospermia	Psma8<em1Yuc>/Psma8<em1Yuc>	C57BL/6-Psma8<em1Yuc>	N	31358751
MGI:6364867	M	MP:0006379	abnormal spermatocyte morphology	Psma8<em1Yuc>/Psma8<em1Yuc>	C57BL/6-Psma8<em1Yuc>	N	31358751
MGI:6364867	M	MP:0008261	arrest of male meiosis	Psma8<em1Yuc>/Psma8<em1Yuc>	C57BL/6-Psma8<em1Yuc>	N	31358751
MGI:6364867	M	MP:0004852	decreased testis weight	Psma8<em1Yuc>/Psma8<em1Yuc>	C57BL/6-Psma8<em1Yuc>	N	31358751
MGI:6364867	M	MP:0001147	small testis	Psma8<em1Yuc>/Psma8<em1Yuc>	C57BL/6-Psma8<em1Yuc>	N	31358751
MGI:6364867	M	MP:0001925	male infertility	Psma8<em1Yuc>/Psma8<em1Yuc>	C57BL/6-Psma8<em1Yuc>	N	31358751
MGI:6364867	F	MP:0005389	reproductive system phenotype	Psma8<em1Yuc>/Psma8<em1Yuc>	C57BL/6-Psma8<em1Yuc>	Y	31358751
MGI:6364867	M	MP:0001156	abnormal spermatogenesis	Psma8<em1Yuc>/Psma8<em1Yuc>	C57BL/6-Psma8<em1Yuc>	N	31358751
MGI:6367580	M	MP:0005365	abnormal bile salt homeostasis	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0005659	decreased susceptibility to diet-induced obesity	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0003868	abnormal feces composition	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0008963	increased carbon dioxide production	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0008770	decreased survivor rate	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0002644	decreased circulating triglyceride level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0000186	decreased circulating HDL cholesterol level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0003961	decreased lean body mass	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0011612	increased circulating ghrelin level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0002064	seizures	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0005289	increased oxygen consumption	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0005319	abnormal enzyme/coenzyme level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0001780	decreased brown adipose tissue amount	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0013278	decreased fasting circulating glucose level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0009305	decreased retroperitoneal fat pad weight	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0005378	growth/size/body region phenotype	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	Y	29491146
MGI:6367580	M	MP:0011972	decreased circulating lactate dehydrogenase level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0005284	increased saturated fatty acids level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0005283	increased unsaturated fatty acids level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0005285	decreased unsaturated fatty acids level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0030969	increased circulating adiponectin level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0010360	decreased liver free fatty acids level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0005668	decreased circulating leptin level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0001405	impaired coordination	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0009356	decreased liver triglyceride level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0005292	improved glucose tolerance	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0002083	premature death	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0014143	decreased body fat mass	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0002891	increased insulin sensitivity	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0009299	decreased mesenteric fat pad weight	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	F	MP:0001386	abnormal maternal nurturing	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0008965	increased basal metabolism	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0000609	abnormal liver physiology	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0004789	increased bile salt level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0005565	increased blood urea nitrogen level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0010155	abnormal intestine physiology	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0005376	homeostasis/metabolism phenotype	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	Y	29491146
MGI:6367580	M	MP:0009293	decreased inguinal fat pad weight	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0005179	decreased circulating cholesterol level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0031391	increased locomotor activity	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0009289	decreased epididymal fat pad weight	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0002968	increased circulating alkaline phosphatase level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0004889	increased energy expenditure	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0011939	increased food intake	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367580	M	MP:0010026	decreased liver cholesterol level	Arv1<tm1.2Geno>/Arv1<tm1.2Geno>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367585	M	MP:0005178	increased circulating cholesterol level	Arv1<tm1.2Geno>/Arv1<+>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367585	M	MP:0001556	increased circulating HDL cholesterol level	Arv1<tm1.2Geno>/Arv1<+>	involves: C57BL/6 * C57BL/6J	N	29491146
MGI:6367636	M	MP:0005386	behavior/neurological phenotype	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	Y	27815211
MGI:6367636	M	MP:0005659	decreased susceptibility to diet-induced obesity	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	N	27815211
MGI:6367636	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	N	27815211
MGI:6367636	M	MP:0003960	increased lean body mass	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	N	27815211
MGI:6367636	M	MP:0002891	increased insulin sensitivity	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	N	27815211
MGI:6367636	M	MP:0011939	increased food intake	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	N	27815211
MGI:6367636	M	MP:0008963	increased carbon dioxide production	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	N	27815211
MGI:6367636	M	MP:0008965	increased basal metabolism	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	N	27815211
MGI:6367636	M	MP:0030994	decreased adipose tissue glycogen level	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	N	27815211
MGI:6367636	M	MP:0002078	abnormal glucose homeostasis	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	N	27815211
MGI:6367636	M	MP:0010398	decreased liver glycogen level	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	N	27815211
MGI:6367636	M	MP:0009289	decreased epididymal fat pad weight	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	N	27815211
MGI:6367636	M	MP:0005289	increased oxygen consumption	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	N	27815211
MGI:6367636	M	MP:0014143	decreased body fat mass	Ppp1r3g<tm1Nju>/Ppp1r3g<tm1Nju>	B6.129-Ppp1r3g<tm1Nju>	N	27815211
MGI:6367658	M	MP:0006380	abnormal spermatid morphology	Rbmxl2<tm1.2Dell>/Rbmxl2<tm1.2Dell>	involves: 129 * BALB/c * C57BL/6 * SJL	N	30674417
MGI:6367658	M	MP:0014052	increased male germ cell apoptosis	Rbmxl2<tm1.2Dell>/Rbmxl2<tm1.2Dell>	involves: 129 * BALB/c * C57BL/6 * SJL	N	30674417
MGI:6367658	M	MP:0005159	azoospermia	Rbmxl2<tm1.2Dell>/Rbmxl2<tm1.2Dell>	involves: 129 * BALB/c * C57BL/6 * SJL	N	30674417
MGI:6367658	F	MP:0005389	reproductive system phenotype	Rbmxl2<tm1.2Dell>/Rbmxl2<tm1.2Dell>	involves: 129 * BALB/c * C57BL/6 * SJL	Y	30674417
MGI:6367658	M	MP:0005621	abnormal cell physiology	Rbmxl2<tm1.2Dell>/Rbmxl2<tm1.2Dell>	involves: 129 * BALB/c * C57BL/6 * SJL	N	30674417
MGI:6367658	M	MP:0008261	arrest of male meiosis	Rbmxl2<tm1.2Dell>/Rbmxl2<tm1.2Dell>	involves: 129 * BALB/c * C57BL/6 * SJL	N	30674417
MGI:6367658	M	MP:0001925	male infertility	Rbmxl2<tm1.2Dell>/Rbmxl2<tm1.2Dell>	involves: 129 * BALB/c * C57BL/6 * SJL	N	30674417
MGI:6367658	M	MP:0001147	small testis	Rbmxl2<tm1.2Dell>/Rbmxl2<tm1.2Dell>	involves: 129 * BALB/c * C57BL/6 * SJL	N	30674417
MGI:6368181	F	MP:0001215	skin hypoplasia	Porcn<tm1.1Lcm>/Porcn<tm1.2Lcm>,Tg(Six3-cre)69Frty/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368181	F	MP:0005262	coloboma	Porcn<tm1.1Lcm>/Porcn<tm1.2Lcm>,Tg(Six3-cre)69Frty/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368181	F	MP:0009264	failure of eyelid fusion	Porcn<tm1.1Lcm>/Porcn<tm1.2Lcm>,Tg(Six3-cre)69Frty/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368181	F	MP:0013283	failure of ventral body wall closure	Porcn<tm1.1Lcm>/Porcn<tm1.2Lcm>,Tg(Six3-cre)69Frty/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368181	F	MP:0012132	abnormal midbrain-hindbrain boundary morphology	Porcn<tm1.1Lcm>/Porcn<tm1.2Lcm>,Tg(Six3-cre)69Frty/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368181	F	MP:0005103	abnormal retina pigmentation	Porcn<tm1.1Lcm>/Porcn<tm1.2Lcm>,Tg(Six3-cre)69Frty/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368181	F	MP:0000428	abnormal craniofacial morphology	Porcn<tm1.1Lcm>/Porcn<tm1.2Lcm>,Tg(Six3-cre)69Frty/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368182	F	MP:0000428	abnormal craniofacial morphology	Porcn<tm1.1Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	25451153
MGI:6368182	F	MP:0009264	failure of eyelid fusion	Porcn<tm1.1Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	25451153
MGI:6368182	F	MP:0012132	abnormal midbrain-hindbrain boundary morphology	Porcn<tm1.1Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	25451153
MGI:6368182	F	MP:0005262	coloboma	Porcn<tm1.1Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	25451153
MGI:6368182	F	MP:0005103	abnormal retina pigmentation	Porcn<tm1.1Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	25451153
MGI:6368183	M	MP:0005103	abnormal retina pigmentation	Porcn<tm1.1Lcm>/Y,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	25451153
MGI:6368183	M	MP:0000428	abnormal craniofacial morphology	Porcn<tm1.1Lcm>/Y,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	25451153
MGI:6368183	M	MP:0005262	coloboma	Porcn<tm1.1Lcm>/Y,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	25451153
MGI:6368183	M	MP:0012132	abnormal midbrain-hindbrain boundary morphology	Porcn<tm1.1Lcm>/Y,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	N	25451153
MGI:6368185	M	MP:0012132	abnormal midbrain-hindbrain boundary morphology	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368185	M	MP:0003935	abnormal craniofacial development	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368185	M	MP:0000111	cleft palate	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368185	M	MP:0031445	midline cleft upper lip	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368185	M	MP:0005262	coloboma	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368185	M	MP:0000428	abnormal craniofacial morphology	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368186	M	MP:0006226	iris hypoplasia	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368186	M	MP:0005193	abnormal anterior eye segment morphology	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368186	M	MP:0012132	abnormal midbrain-hindbrain boundary morphology	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368186	M	MP:0000111	cleft palate	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368186	M	MP:0005103	abnormal retina pigmentation	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368186	M	MP:0009264	failure of eyelid fusion	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368186	M	MP:0031445	midline cleft upper lip	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368186	M	MP:0000428	abnormal craniofacial morphology	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368186	M	MP:0005262	coloboma	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368186	M	MP:0005543	decreased cornea thickness	Porcn<tm1.1Lcm>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368187	F	MP:0005103	abnormal retina pigmentation	Porcn<tm1.1Lcm>/Porcn<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368187	F	MP:0005262	coloboma	Porcn<tm1.1Lcm>/Porcn<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368187	F	MP:0001297	microphthalmia	Porcn<tm1.1Lcm>/Porcn<+>,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>,Tg(rx3-icre)1Mjam/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	N	25451153
MGI:6368188	F	MP:0000428	abnormal craniofacial morphology	Porcn<tm1.2Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368188	F	MP:0009264	failure of eyelid fusion	Porcn<tm1.2Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368188	F	MP:0014280	forelimb oligodactyly	Porcn<tm1.2Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368188	F	MP:0012132	abnormal midbrain-hindbrain boundary morphology	Porcn<tm1.2Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368188	F	MP:0005103	abnormal retina pigmentation	Porcn<tm1.2Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368188	F	MP:0000592	short tail	Porcn<tm1.2Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368188	F	MP:0005262	coloboma	Porcn<tm1.2Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368188	F	MP:0000564	syndactyly	Porcn<tm1.2Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368188	F	MP:0003051	curly tail	Porcn<tm1.2Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368188	F	MP:0004073	caudal body truncation	Porcn<tm1.2Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368188	F	MP:0002109	abnormal limb morphology	Porcn<tm1.2Lcm>/Porcn<tm1.2Lcm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	N	25451153
MGI:6368191	M	MP:0005293	impaired glucose tolerance	Myrip<tm1Tiz>/Myrip<tm1Tiz>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	28673385
MGI:6368191	M	MP:0001262	decreased body weight	Myrip<tm1Tiz>/Myrip<tm1Tiz>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	28673385
MGI:6368191	M	MP:0005215	abnormal pancreatic islet morphology	Myrip<tm1Tiz>/Myrip<tm1Tiz>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	28673385
MGI:6368191	M	MP:0003059	decreased insulin secretion	Myrip<tm1Tiz>/Myrip<tm1Tiz>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	28673385
MGI:6368191	M	MP:0005217	abnormal pancreatic beta cell morphology	Myrip<tm1Tiz>/Myrip<tm1Tiz>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	28673385
MGI:6368194	M	MP:0014169	decreased brown adipose tissue mass	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0014146	decreased white adipose tissue mass	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0011939	increased food intake	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0020254	decreased collagen level	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0005669	increased circulating leptin level	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0002970	abnormal white adipose tissue morphology	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0005370	liver/biliary system phenotype	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	Y	28559441
MGI:6368194	M	MP:0005668	decreased circulating leptin level	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0002891	increased insulin sensitivity	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0005390	skeleton phenotype	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	Y	28559441
MGI:6368194	M	MP:0010378	increased respiratory quotient	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0013258	abnormal extracellular matrix morphology	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0005560	decreased circulating glucose level	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0005670	abnormal white adipose tissue physiology	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0009133	decreased white fat cell size	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0005378	growth/size/body region phenotype	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	Y	28559441
MGI:6368194	M	MP:0009130	increased white fat cell number	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368194	M	MP:0005292	improved glucose tolerance	Apmap<tm1.2Jgbs>/Apmap<tm1.2Jgbs>	B6.129P2-Apmap<tm1.2Jgbs>	N	28559441
MGI:6368204	M	MP:0001925	male infertility	Gpat2<tm1.1Nkn>/Gpat2<tm1.1Nkn>	involves: 129S2/SvPas * C57BL/6NSlc	N	30951587
MGI:6368204	M	MP:0008878	abnormal DNA methylation during gametogenesis	Gpat2<tm1.1Nkn>/Gpat2<tm1.1Nkn>	involves: 129S2/SvPas * C57BL/6NSlc	N	30951587
MGI:6368204	M	MP:0005159	azoospermia	Gpat2<tm1.1Nkn>/Gpat2<tm1.1Nkn>	involves: 129S2/SvPas * C57BL/6NSlc	N	30951587
MGI:6368204	M	MP:0004852	decreased testis weight	Gpat2<tm1.1Nkn>/Gpat2<tm1.1Nkn>	involves: 129S2/SvPas * C57BL/6NSlc	N	30951587
MGI:6368204	F	MP:0005389	reproductive system phenotype	Gpat2<tm1.1Nkn>/Gpat2<tm1.1Nkn>	involves: 129S2/SvPas * C57BL/6NSlc	Y	30951587
MGI:6368204	M	MP:0006362	abnormal male germ cell morphology	Gpat2<tm1.1Nkn>/Gpat2<tm1.1Nkn>	involves: 129S2/SvPas * C57BL/6NSlc	N	30951587
MGI:6368204	M	MP:0001147	small testis	Gpat2<tm1.1Nkn>/Gpat2<tm1.1Nkn>	involves: 129S2/SvPas * C57BL/6NSlc	N	30951587
MGI:6368204	M	MP:0006379	abnormal spermatocyte morphology	Gpat2<tm1.1Nkn>/Gpat2<tm1.1Nkn>	involves: 129S2/SvPas * C57BL/6NSlc	N	30951587
MGI:6368204	M	MP:0014052	increased male germ cell apoptosis	Gpat2<tm1.1Nkn>/Gpat2<tm1.1Nkn>	involves: 129S2/SvPas * C57BL/6NSlc	N	30951587
MGI:6368213	M	MP:0005382	craniofacial phenotype	Phf8<tm1.1Hoch>/Y	involves: 129S4/SvJae * C57BL/6	Y	28485378
MGI:6368213	M	MP:0004077	abnormal striatum morphology	Phf8<tm1.1Hoch>/Y	involves: 129S4/SvJae * C57BL/6	N	28485378
MGI:6368213	M	MP:0003063	increased coping response	Phf8<tm1.1Hoch>/Y	involves: 129S4/SvJae * C57BL/6	N	28485378
MGI:6368213	M	MP:0000352	decreased cell proliferation	Phf8<tm1.1Hoch>/Y	involves: 129S4/SvJae * C57BL/6	N	28485378
MGI:6368213	M	MP:0020870	decreased thigmotaxis	Phf8<tm1.1Hoch>/Y	involves: 129S4/SvJae * C57BL/6	N	28485378
MGI:6368213	M	MP:0001364	decreased anxiety-related response	Phf8<tm1.1Hoch>/Y	involves: 129S4/SvJae * C57BL/6	N	28485378
MGI:6368213	M	MP:0005378	growth/size/body region phenotype	Phf8<tm1.1Hoch>/Y	involves: 129S4/SvJae * C57BL/6	Y	28485378
MGI:6368559	M	MP:0008450	retina photoreceptor degeneration	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0008515	thin retina outer nuclear layer	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0008587	short photoreceptor outer segment	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0008586	disorganized photoreceptor outer segment	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0030988	dysosmia	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0014059	abnormal photoreceptor connecting cilium morphology	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0001891	hydrocephaly	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0012143	decreased a-wave amplitude	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0004022	abnormal cone electrophysiology	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0001935	decreased litter size	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0011101	prenatal lethality, incomplete penetrance	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0004021	abnormal rod electrophysiology	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0012144	decreased b-wave amplitude	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0020813	abnormal photoreceptor outer segment disc membrane morphology	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0008449	abnormal retina cone cell outer segment morphology	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368559	M	MP:0020814	abnormal photoreceptor outer segment diameter	Cetn2<tm1.1Wbae>/Y,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368609	F	MP:0012144	decreased b-wave amplitude	Cetn2<tm1.1Wbae>/Cetn2<+>,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368609	F	MP:0004021	abnormal rod electrophysiology	Cetn2<tm1.1Wbae>/Cetn2<+>,Cetn3<tm1a(EUCOMM)Wtsi>/Cetn3<tm1a(EUCOMM)Wtsi>	involves: 129 * C57BL/6J * C57BL/6N * FVB/N	N	30647131
MGI:6368622	M	MP:0009118	increased white fat cell size	Cyp4x1<tm1.1Beld>/Cyp4x1<tm1.1Beld>	involves: C57BL/6	N	29227996
MGI:6368622	M	MP:0009288	increased epididymal fat pad weight	Cyp4x1<tm1.1Beld>/Cyp4x1<tm1.1Beld>	involves: C57BL/6	N	29227996
MGI:6368622	M	MP:0010379	decreased respiratory quotient	Cyp4x1<tm1.1Beld>/Cyp4x1<tm1.1Beld>	involves: C57BL/6	N	29227996
MGI:6368622	F	MP:0001402	decreased locomotor activity	Cyp4x1<tm1.1Beld>/Cyp4x1<tm1.1Beld>	involves: C57BL/6	N	29227996
MGI:6368622	M	MP:0020411	increased abdominal adipose tissue amount	Cyp4x1<tm1.1Beld>/Cyp4x1<tm1.1Beld>	involves: C57BL/6	N	29227996
MGI:6368622	F	MP:0005658	increased susceptibility to diet-induced obesity	Cyp4x1<tm1.1Beld>/Cyp4x1<tm1.1Beld>	involves: C57BL/6	N	29227996
MGI:6368806	M	MP:0001925	male infertility	Stk33<tm1.2Csll>/Stk33<tm1.2Csll>	B6.Cg-Stk33<tm1.2Csll>	N	29155043
MGI:6368806	M	MP:0002675	asthenozoospermia	Stk33<tm1.2Csll>/Stk33<tm1.2Csll>	B6.Cg-Stk33<tm1.2Csll>	N	29155043
MGI:6368806	M	MP:0008892	abnormal sperm flagellum morphology	Stk33<tm1.2Csll>/Stk33<tm1.2Csll>	B6.Cg-Stk33<tm1.2Csll>	N	29155043
MGI:6368873	M	MP:0001146	abnormal testis morphology	Nr5a1<em1Kemi>/Nr5a1<em1Kemi>	involves: C57BL/6 * DBA/2	N	27833742
MGI:6368873	M	MP:0001939	secondary sex reversal	Nr5a1<em1Kemi>/Nr5a1<em1Kemi>	involves: C57BL/6 * DBA/2	N	27833742
MGI:6368873	F	MP:0005389	reproductive system phenotype	Nr5a1<em1Kemi>/Nr5a1<em1Kemi>	involves: C57BL/6 * DBA/2	Y	27833742
MGI:6368873	F	MP:0001116	small gonad	Nr5a1<em1Kemi>/Nr5a1<em1Kemi>	involves: C57BL/6 * DBA/2	N	27833742
MGI:6368873	M	MP:0001116	small gonad	Nr5a1<em1Kemi>/Nr5a1<em1Kemi>	involves: C57BL/6 * DBA/2	N	27833742
MGI:6368882	M	MP:0002687	oligozoospermia	Tppp2<em1Nju>/Tppp2<em1Nju>	Not Specified	N	30680919
MGI:6368882	M	MP:0001922	reduced male fertility	Tppp2<em1Nju>/Tppp2<em1Nju>	Not Specified	N	30680919
MGI:6368882	M	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport	Tppp2<em1Nju>/Tppp2<em1Nju>	Not Specified	N	30680919
MGI:6368882	M	MP:0002675	asthenozoospermia	Tppp2<em1Nju>/Tppp2<em1Nju>	Not Specified	N	30680919
MGI:6368882	M	MP:0014052	increased male germ cell apoptosis	Tppp2<em1Nju>/Tppp2<em1Nju>	Not Specified	N	30680919
MGI:6368882	M	MP:0001935	decreased litter size	Tppp2<em1Nju>/Tppp2<em1Nju>	Not Specified	N	30680919
MGI:6368882	M	MP:0006035	abnormal mitochondrial morphology	Tppp2<em1Nju>/Tppp2<em1Nju>	Not Specified	N	30680919
MGI:6368884	M	MP:0001147	small testis	Nr5a1<em1Kemi>/Nr5a1<+>	involves: C57BL/6 * DBA/2	N	27833742
MGI:6369061	M	MP:0009836	abnormal sperm principal piece morphology	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0009238	coiled sperm flagellum	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0009831	abnormal sperm midpiece morphology	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0009834	abnormal sperm annulus morphology	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0009239	short sperm flagellum	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0001925	male infertility	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0008892	abnormal sperm flagellum morphology	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0009830	abnormal sperm connecting piece morphology	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0009838	abnormal sperm axoneme morphology	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0031352	absent sperm axonemal central pair	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0008893	detached sperm flagellum	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0020451	decreased sperm progressive motility	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0009237	kinked sperm flagellum	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0001935	decreased litter size	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0001932	abnormal spermiogenesis	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0002675	asthenozoospermia	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0005578	teratozoospermia	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369061	M	MP:0009837	abnormal sperm end piece morphology	Ttc21a<em1Fzh>/Ttc21a<em1Fzh>	involves: C57BL/6	N	30929735
MGI:6369094	M	MP:0002674	abnormal sperm motility	Crisp2<tm1a(KOMP)Mbp>/Crisp2<tm1a(KOMP)Mbp>	C57BL/6N-Crisp2<tm1a(KOMP)Mbp>	N	30759213
MGI:6369094	M	MP:0001922	reduced male fertility	Crisp2<tm1a(KOMP)Mbp>/Crisp2<tm1a(KOMP)Mbp>	C57BL/6N-Crisp2<tm1a(KOMP)Mbp>	N	30759213
MGI:6369094	M	MP:0004542	impaired acrosome reaction	Crisp2<tm1a(KOMP)Mbp>/Crisp2<tm1a(KOMP)Mbp>	C57BL/6N-Crisp2<tm1a(KOMP)Mbp>	N	30759213
MGI:6369094	M	MP:0020451	decreased sperm progressive motility	Crisp2<tm1a(KOMP)Mbp>/Crisp2<tm1a(KOMP)Mbp>	C57BL/6N-Crisp2<tm1a(KOMP)Mbp>	N	30759213
MGI:6369094	F	MP:0005389	reproductive system phenotype	Crisp2<tm1a(KOMP)Mbp>/Crisp2<tm1a(KOMP)Mbp>	C57BL/6N-Crisp2<tm1a(KOMP)Mbp>	Y	30759213
MGI:6369094	M	MP:0002675	asthenozoospermia	Crisp2<tm1a(KOMP)Mbp>/Crisp2<tm1a(KOMP)Mbp>	C57BL/6N-Crisp2<tm1a(KOMP)Mbp>	N	30759213
MGI:6369095	M	MP:0020451	decreased sperm progressive motility	Crisp2<tm1c(KOMP)Mbp>/Crisp2<tm1c(KOMP)Mbp>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	30759213
MGI:6369095	F	MP:0005389	reproductive system phenotype	Crisp2<tm1c(KOMP)Mbp>/Crisp2<tm1c(KOMP)Mbp>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	Y	30759213
MGI:6369095	M	MP:0001922	reduced male fertility	Crisp2<tm1c(KOMP)Mbp>/Crisp2<tm1c(KOMP)Mbp>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	30759213
MGI:6369095	M	MP:0002675	asthenozoospermia	Crisp2<tm1c(KOMP)Mbp>/Crisp2<tm1c(KOMP)Mbp>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	30759213
MGI:6369095	M	MP:0004542	impaired acrosome reaction	Crisp2<tm1c(KOMP)Mbp>/Crisp2<tm1c(KOMP)Mbp>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	30759213
MGI:6369369	F	MP:0001364	decreased anxiety-related response	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0011965	decreased total retina thickness	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0000745	tremors	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0011954	shortened PQ interval	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0005559	increased circulating glucose level	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0011925	abnormal heart echocardiography feature	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	M	MP:0001260	increased body weight	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0010876	decreased bone volume	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0010379	decreased respiratory quotient	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0002702	decreased circulating free fatty acids level	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0011940	decreased food intake	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0011952	decreased cardiac stroke volume	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	M	MP:0002875	decreased erythrocyte cell number	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0010511	shortened PR interval	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	M	MP:0002981	increased liver weight	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0006086	decreased body mass index	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	M	MP:0000218	increased leukocyte cell number	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	M	MP:0005561	increased mean corpuscular hemoglobin	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	M	MP:0000248	macrocytosis	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	M	MP:0004952	increased spleen weight	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0005599	increased cardiac muscle contractility	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0001258	decreased body length	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0014142	increased body fat mass	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369369	F	MP:0010124	decreased bone mineral content	Cldn12<tm1.1(KOMP)Vlcg>/Cldn12<tm1.1(KOMP)Vlcg>	B6J.B6N-Cldn12<tm1.1(KOMP)Vlcg>	N	31511021
MGI:6369414	M	MP:0002626	increased heart rate	Rcn2<tm1b(KOMP)Wtsi>/Rcn2<tm1b(KOMP)Wtsi>	involves: C3H * C57BL/6 * C57BL/6N	N	30943068
MGI:6369414	M	MP:0002843	decreased systemic arterial blood pressure	Rcn2<tm1b(KOMP)Wtsi>/Rcn2<tm1b(KOMP)Wtsi>	involves: C3H * C57BL/6 * C57BL/6N	N	30943068
MGI:6369414	M	MP:0005367	renal/urinary system phenotype	Rcn2<tm1b(KOMP)Wtsi>/Rcn2<tm1b(KOMP)Wtsi>	involves: C3H * C57BL/6 * C57BL/6N	Y	30943068
MGI:6369414	M	MP:0000249	abnormal blood vessel physiology	Rcn2<tm1b(KOMP)Wtsi>/Rcn2<tm1b(KOMP)Wtsi>	involves: C3H * C57BL/6 * C57BL/6N	N	30943068
MGI:6369414	M	MP:0012046	decreased susceptibility to hypertension	Rcn2<tm1b(KOMP)Wtsi>/Rcn2<tm1b(KOMP)Wtsi>	involves: C3H * C57BL/6 * C57BL/6N	N	30943068
MGI:6369630	M	MP:0008545	absent sperm flagellum	Armc2<em1Pfr>/Armc2<em1Pfr>	Not Specified	N	30686508
MGI:6369630	M	MP:0009241	thick sperm flagellum	Armc2<em1Pfr>/Armc2<em1Pfr>	Not Specified	N	30686508
MGI:6369630	F	MP:0005389	reproductive system phenotype	Armc2<em1Pfr>/Armc2<em1Pfr>	Not Specified	Y	30686508
MGI:6369630	M	MP:0031352	absent sperm axonemal central pair	Armc2<em1Pfr>/Armc2<em1Pfr>	Not Specified	N	30686508
MGI:6369630	M	MP:0009238	coiled sperm flagellum	Armc2<em1Pfr>/Armc2<em1Pfr>	Not Specified	N	30686508
MGI:6369630	M	MP:0001925	male infertility	Armc2<em1Pfr>/Armc2<em1Pfr>	Not Specified	N	30686508
MGI:6369630	M	MP:0008892	abnormal sperm flagellum morphology	Armc2<em1Pfr>/Armc2<em1Pfr>	Not Specified	N	30686508
MGI:6369630	M	MP:0020869	immotile sperm	Armc2<em1Pfr>/Armc2<em1Pfr>	Not Specified	N	30686508
MGI:6369630	M	MP:0002687	oligozoospermia	Armc2<em1Pfr>/Armc2<em1Pfr>	Not Specified	N	30686508
MGI:6369630	M	MP:0009239	short sperm flagellum	Armc2<em1Pfr>/Armc2<em1Pfr>	Not Specified	N	30686508
MGI:6369630	M	MP:0005578	teratozoospermia	Armc2<em1Pfr>/Armc2<em1Pfr>	Not Specified	N	30686508
MGI:6369650	M	MP:0001153	small seminiferous tubules	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30807788
MGI:6369650	M	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30807788
MGI:6369650	M	MP:0004852	decreased testis weight	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30807788
MGI:6369650	M	MP:0005389	reproductive system phenotype	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	Y	30807788
MGI:6369650	M	MP:0003674	oxidative stress	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30807788
MGI:6369650	M	MP:0013601	increased testis apoptosis	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30807788
MGI:6369650	M	MP:0009325	necrospermia	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30807788
MGI:6369650	M	MP:0005578	teratozoospermia	Ide<tm1a(EUCOMM)Wtsi>/Ide<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	30807788
MGI:6369655	M	MP:0004852	decreased testis weight	Ide<tm1a(EUCOMM)Wtsi>/Ide<+>	involves: C57BL/6N	N	30807788
MGI:6369655	M	MP:0005389	reproductive system phenotype	Ide<tm1a(EUCOMM)Wtsi>/Ide<+>	involves: C57BL/6N	Y	30807788
MGI:6369716	M	MP:0001925	male infertility	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0001147	small testis	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0004930	small epididymis	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0005159	azoospermia	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0004109	abnormal Sertoli cell development	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0001154	seminiferous tubule degeneration	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0002216	abnormal seminiferous tubule morphology	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0001751	increased circulating luteinizing hormone level	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0009257	dilated seminiferous tubule	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0006380	abnormal spermatid morphology	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0001156	abnormal spermatogenesis	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0004884	abnormal testis physiology	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0004901	decreased male germ cell number	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0001750	increased circulating follicle stimulating hormone level	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0001155	arrest of spermatogenesis	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0006378	abnormal spermatogonia morphology	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0004929	decreased epididymis weight	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0004852	decreased testis weight	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369716	M	MP:0013601	increased testis apoptosis	Arid4b<tm1Alb>/Arid4b<tm1.1Mywu>,Tg(Amh-cre)8815Reb/0	involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	N	26258622
MGI:6369793	M	MP:0009747	impaired behavioral response to xenobiotic	Mir425<em1Nju>/Mir425<+>	involves: C57BL/6	N	31383850
MGI:6369793	M	MP:0003244	loss of dopaminergic neurons	Mir425<em1Nju>/Mir425<+>	involves: C57BL/6	N	31383850
MGI:6369793	M	MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity	Mir425<em1Nju>/Mir425<+>	involves: C57BL/6	N	31383850
MGI:6369793	M	MP:0008560	increased tumor necrosis factor secretion	Mir425<em1Nju>/Mir425<+>	involves: C57BL/6	N	31383850
MGI:6370003	M	MP:0005382	craniofacial phenotype	Phf8<tm1.1Cdcn>/Y	B6.129S6(Cg)-Phf8<tm1.1Cdcn>	Y	29317619
MGI:6370003	M	MP:0012307	impaired spatial learning	Phf8<tm1.1Cdcn>/Y	B6.129S6(Cg)-Phf8<tm1.1Cdcn>	N	29317619
MGI:6370003	M	MP:0008414	abnormal spatial reference memory	Phf8<tm1.1Cdcn>/Y	B6.129S6(Cg)-Phf8<tm1.1Cdcn>	N	29317619
MGI:6370003	M	MP:0001473	reduced long-term potentiation	Phf8<tm1.1Cdcn>/Y	B6.129S6(Cg)-Phf8<tm1.1Cdcn>	N	29317619
MGI:6370003	M	MP:0031391	increased locomotor activity	Phf8<tm1.1Cdcn>/Y	B6.129S6(Cg)-Phf8<tm1.1Cdcn>	N	29317619
MGI:6370003	M	MP:0009454	impaired contextual conditioning behavior	Phf8<tm1.1Cdcn>/Y	B6.129S6(Cg)-Phf8<tm1.1Cdcn>	N	29317619
MGI:6370003	M	MP:0004000	impaired passive avoidance behavior	Phf8<tm1.1Cdcn>/Y	B6.129S6(Cg)-Phf8<tm1.1Cdcn>	N	29317619
MGI:6370003	M	MP:0003635	abnormal synaptic transmission	Phf8<tm1.1Cdcn>/Y	B6.129S6(Cg)-Phf8<tm1.1Cdcn>	N	29317619
MGI:6370045	M	MP:0009456	impaired cued conditioning behavior	Bbs4<Gt1Nk>/Bbs4<Gt1Nk>	B6.129S7-Bbs4<Gt1Nk>	N	31479441
MGI:6370045	F	MP:0009454	impaired contextual conditioning behavior	Bbs4<Gt1Nk>/Bbs4<Gt1Nk>	B6.129S7-Bbs4<Gt1Nk>	N	31479441
MGI:6370382	F	MP:0011962	increased cornea thickness	Trappc2b<tm1b(EUCOMM)Hmgu>/Trappc2b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trappc2b<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6370383	F	MP:0010052	increased grip strength	Abca16<em1(IMPC)J>/Abca16<em1(IMPC)J>	C57BL/6NJ-Abca16<em1(IMPC)J>/J	N	MGI:5576271
MGI:6370383	F	MP:0001303	abnormal lens morphology	Abca16<em1(IMPC)J>/Abca16<em1(IMPC)J>	C57BL/6NJ-Abca16<em1(IMPC)J>/J	N	MGI:5576271
MGI:6370383	F	MP:0005634	decreased circulating sodium level	Abca16<em1(IMPC)J>/Abca16<em1(IMPC)J>	C57BL/6NJ-Abca16<em1(IMPC)J>/J	N	MGI:5576271
MGI:6370384	F	MP:0001399	hyperactivity	Adam20<tm1b(EUCOMM)Hmgu>/Adam20<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adam20<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6370386	F	MP:0002941	increased circulating alanine transaminase level	Als2cl<em1(IMPC)J>/Als2cl<em1(IMPC)J>	C57BL/6NJ-Als2cl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370389	F	MP:0010506	prolonged RR interval	Arv1<em1(IMPC)J>/Arv1<em1(IMPC)J>	C57BL/6NJ-Arv1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370389	M	MP:0002797	increased thigmotaxis	Arv1<em1(IMPC)J>/Arv1<em1(IMPC)J>	C57BL/6NJ-Arv1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370389	F	MP:0005293	impaired glucose tolerance	Arv1<em1(IMPC)J>/Arv1<em1(IMPC)J>	C57BL/6NJ-Arv1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370389	F	MP:0005333	decreased heart rate	Arv1<em1(IMPC)J>/Arv1<em1(IMPC)J>	C57BL/6NJ-Arv1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370389	F	MP:0010052	increased grip strength	Arv1<em1(IMPC)J>/Arv1<em1(IMPC)J>	C57BL/6NJ-Arv1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370389	F	MP:0000063	decreased bone mineral density	Arv1<em1(IMPC)J>/Arv1<em1(IMPC)J>	C57BL/6NJ-Arv1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370390	F	MP:0001340	abnormal eyelid morphology	Awat2<em1(IMPC)Mbp>/Awat2<em1(IMPC)Mbp>	C57BL/6NCrl-Awat2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370390	F	MP:0002092	abnormal eye morphology	Awat2<em1(IMPC)Mbp>/Awat2<em1(IMPC)Mbp>	C57BL/6NCrl-Awat2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370390	F	MP:0005343	increased circulating aspartate transaminase level	Awat2<em1(IMPC)Mbp>/Awat2<em1(IMPC)Mbp>	C57BL/6NCrl-Awat2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370390	F	MP:0006203	eye hemorrhage	Awat2<em1(IMPC)Mbp>/Awat2<em1(IMPC)Mbp>	C57BL/6NCrl-Awat2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370390	F	MP:0001944	abnormal pancreas morphology	Awat2<em1(IMPC)Mbp>/Awat2<em1(IMPC)Mbp>	C57BL/6NCrl-Awat2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370391	M	MP:0000063	decreased bone mineral density	Cep135<em1(IMPC)J>/Cep135<+>	C57BL/6NJ-Cep135<em1(IMPC)J>/J	N	MGI:5576271
MGI:6370392	F	MP:0001120	abnormal uterus morphology	Chmp2b<em1(IMPC)Mbp>/Chmp2b<+>	C57BL/6NCrl-Chmp2b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370392	F	MP:0009084	blind uterus	Chmp2b<em1(IMPC)Mbp>/Chmp2b<+>	C57BL/6NCrl-Chmp2b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370392	F	MP:0005333	decreased heart rate	Chmp2b<em1(IMPC)Mbp>/Chmp2b<+>	C57BL/6NCrl-Chmp2b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370392	M	MP:0002997	enlarged seminal vesicle	Chmp2b<em1(IMPC)Mbp>/Chmp2b<+>	C57BL/6NCrl-Chmp2b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370392	M	MP:0001146	abnormal testis morphology	Chmp2b<em1(IMPC)Mbp>/Chmp2b<+>	C57BL/6NCrl-Chmp2b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370392	F	MP:0010506	prolonged RR interval	Chmp2b<em1(IMPC)Mbp>/Chmp2b<+>	C57BL/6NCrl-Chmp2b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370392	F	MP:0002135	abnormal kidney morphology	Chmp2b<em1(IMPC)Mbp>/Chmp2b<+>	C57BL/6NCrl-Chmp2b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370392	F	MP:0002989	small kidney	Chmp2b<em1(IMPC)Mbp>/Chmp2b<+>	C57BL/6NCrl-Chmp2b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370392	M	MP:0001147	small testis	Chmp2b<em1(IMPC)Mbp>/Chmp2b<+>	C57BL/6NCrl-Chmp2b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370392	M	MP:0003642	absent seminal vesicle	Chmp2b<em1(IMPC)Mbp>/Chmp2b<+>	C57BL/6NCrl-Chmp2b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370392	M	MP:0000598	abnormal liver morphology	Chmp2b<em1(IMPC)Mbp>/Chmp2b<+>	C57BL/6NCrl-Chmp2b<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370395	F	MP:0003733	abnormal retina inner nuclear layer morphology	Csk<tm2b(EUCOMM)Hmgu>/Csk<+>	C57BL/6N-Csk<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6370397	M	MP:0002631	abnormal epididymis morphology	Katnip<em1(IMPC)Mbp>/Katnip<+>	C57BL/6NCrl-Katnip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370397	M	MP:0001304	cataract	Katnip<em1(IMPC)Mbp>/Katnip<+>	C57BL/6NCrl-Katnip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370397	F	MP:0000639	abnormal adrenal gland morphology	Katnip<em1(IMPC)Mbp>/Katnip<+>	C57BL/6NCrl-Katnip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370397	M	MP:0004931	enlarged epididymis	Katnip<em1(IMPC)Mbp>/Katnip<+>	C57BL/6NCrl-Katnip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370397	M	MP:0001402	decreased locomotor activity	Katnip<em1(IMPC)Mbp>/Katnip<+>	C57BL/6NCrl-Katnip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370399	M	MP:0004002	abnormal jejunum morphology	E2f3<tm1b(KOMP)Wtsi>/E2f3<+>	C57BL/6N-E2f3<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6370402	F	MP:0005011	increased eosinophil cell number	Fbxl18<tm1b(EUCOMM)Hmgu>/Fbxl18<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fbxl18<tm1b(EUCOMM)Hmgu>/Mhzh	N	MGI:5576271
MGI:6370402	F	MP:0002606	increased basophil cell number	Fbxl18<tm1b(EUCOMM)Hmgu>/Fbxl18<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fbxl18<tm1b(EUCOMM)Hmgu>/Mhzh	N	MGI:5576271
MGI:6370404	F	MP:0001417	decreased exploration in new environment	Foxred2<tm1.1(KOMP)Vlcg>/Foxred2<tm1.1(KOMP)Vlcg>	C57BL/6N-Foxred2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6370405	M	MP:0020870	decreased thigmotaxis	Fubp1<em1(IMPC)Mbp>/Fubp1<+>	C57BL/6N-Fubp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6370405	F	MP:0002060	abnormal skin morphology	Fubp1<em1(IMPC)Mbp>/Fubp1<+>	C57BL/6N-Fubp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6370405	M	MP:0001364	decreased anxiety-related response	Fubp1<em1(IMPC)Mbp>/Fubp1<+>	C57BL/6N-Fubp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6370405	M	MP:0001402	decreased locomotor activity	Fubp1<em1(IMPC)Mbp>/Fubp1<+>	C57BL/6N-Fubp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6370405	F	MP:0001325	abnormal retina morphology	Fubp1<em1(IMPC)Mbp>/Fubp1<+>	C57BL/6N-Fubp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6370405	M	MP:0000702	enlarged lymph nodes	Fubp1<em1(IMPC)Mbp>/Fubp1<+>	C57BL/6N-Fubp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6370405	M	MP:0004924	abnormal behavior	Fubp1<em1(IMPC)Mbp>/Fubp1<+>	C57BL/6N-Fubp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6370405	M	MP:0002339	abnormal lymph node morphology	Fubp1<em1(IMPC)Mbp>/Fubp1<+>	C57BL/6N-Fubp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6370407	M	MP:0000639	abnormal adrenal gland morphology	Gfm2<em1(IMPC)Mbp>/Gfm2<+>	C57BL/6N-Gfm2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6370408	F	MP:0003731	abnormal retina outer nuclear layer morphology	Ginm1<tm1b(EUCOMM)Wtsi>/Ginm1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ginm1<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6370408	M	MP:0008259	abnormal optic disk morphology	Ginm1<tm1b(EUCOMM)Wtsi>/Ginm1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ginm1<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6370408	F	MP:0011110	preweaning lethality, incomplete penetrance	Ginm1<tm1b(EUCOMM)Wtsi>/Ginm1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ginm1<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6370410	M	MP:0001406	abnormal gait	Gpr156<tm1.1(KOMP)Vlcg>/Gpr156<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpr156<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6370413	M	MP:0001566	increased circulating phosphate level	Igsf9<em1(IMPC)J>/Igsf9<em1(IMPC)J>	C57BL/6NJ-Igsf9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370413	F	MP:0010052	increased grip strength	Igsf9<em1(IMPC)J>/Igsf9<em1(IMPC)J>	C57BL/6NJ-Igsf9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370416	F	MP:0001303	abnormal lens morphology	Klkb1<tm1b(EUCOMM)Wtsi>/Klkb1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Klkb1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6370418	M	MP:0002608	increased hematocrit	Lyplal1<tm1b(KOMP)Wtsi>/Lyplal1<tm1b(KOMP)Wtsi>	C57BL/6N-Lyplal1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6370418	F	MP:0002591	decreased mean corpuscular volume	Lyplal1<tm1b(KOMP)Wtsi>/Lyplal1<tm1b(KOMP)Wtsi>	C57BL/6N-Lyplal1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6370420	F	MP:0001304	cataract	Mon1a<em1(IMPC)J>/Mon1a<em1(IMPC)J>	C57BL/6NJ-Mon1a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6370420	F	MP:0013278	decreased fasting circulating glucose level	Mon1a<em1(IMPC)J>/Mon1a<em1(IMPC)J>	C57BL/6NJ-Mon1a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6370421	F	MP:0002092	abnormal eye morphology	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0003179	thrombocytopenia	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0010124	decreased bone mineral content	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0002997	enlarged seminal vesicle	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0001402	decreased locomotor activity	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	F	MP:0010052	increased grip strength	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0002188	small heart	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0000692	small spleen	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0008528	polycystic kidney	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0002059	abnormal seminal vesicle morphology	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0002834	decreased heart weight	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0000063	decreased bone mineral density	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	F	MP:0000689	abnormal spleen morphology	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0000266	abnormal heart morphology	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0000598	abnormal liver morphology	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0004924	abnormal behavior	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0001364	decreased anxiety-related response	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0020870	decreased thigmotaxis	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	F	MP:0002339	abnormal lymph node morphology	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	M	MP:0003642	absent seminal vesicle	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	F	MP:0002060	abnormal skin morphology	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370421	F	MP:0000691	enlarged spleen	Nucb1<em1(IMPC)Mbp>/Nucb1<em1(IMPC)Mbp>	C57BL/6NCrl-Nucb1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370423	M	MP:0002631	abnormal epididymis morphology	Paqr8<em1(IMPC)Mbp>/Paqr8<em1(IMPC)Mbp>	C57BL/6N-Paqr8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6370423	M	MP:0004931	enlarged epididymis	Paqr8<em1(IMPC)Mbp>/Paqr8<em1(IMPC)Mbp>	C57BL/6N-Paqr8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6370425	F	MP:0001523	impaired righting response	Polr1c<em1(IMPC)J>/Polr1c<+>	C57BL/6NJ-Polr1c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370426	M	MP:0020870	decreased thigmotaxis	Prr15l<tm1.1(KOMP)Vlcg>/Prr15l<tm1.1(KOMP)Vlcg>	C57BL/6N-Prr15l<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6370426	M	MP:0004924	abnormal behavior	Prr15l<tm1.1(KOMP)Vlcg>/Prr15l<tm1.1(KOMP)Vlcg>	C57BL/6N-Prr15l<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6370427	F	MP:0003731	abnormal retina outer nuclear layer morphology	Rd3<em1(IMPC)Bay>/Rd3<em1(IMPC)Bay>	C57BL/6N-Rd3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6370427	F	MP:0011959	abnormal eye posterior chamber depth	Rd3<em1(IMPC)Bay>/Rd3<em1(IMPC)Bay>	C57BL/6N-Rd3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6370427	F	MP:0011960	abnormal eye anterior chamber depth	Rd3<em1(IMPC)Bay>/Rd3<em1(IMPC)Bay>	C57BL/6N-Rd3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6370428	M	MP:0010067	increased red blood cell distribution width	Rinl<em1(IMPC)Mbp>/Rinl<em1(IMPC)Mbp>	C57BL/6NCrl-Rinl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370431	F	MP:0001325	abnormal retina morphology	S100a14<tm1b(EUCOMM)Hmgu>/S100a14<+>	C57BL/6N-S100a14<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:6370432	M	MP:0000194	increased circulating calcium level	Samd9l<tm1.1(KOMP)Wtsi>/Samd9l<tm1.1(KOMP)Wtsi>	C57BL/6N-Samd9l<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6370432	M	MP:0001566	increased circulating phosphate level	Samd9l<tm1.1(KOMP)Wtsi>/Samd9l<tm1.1(KOMP)Wtsi>	C57BL/6N-Samd9l<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6370433	F	MP:0000689	abnormal spleen morphology	Serpinb10<em1(IMPC)Mbp>/Serpinb10<em1(IMPC)Mbp>	C57BL/6NCrl-Serpinb10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370433	F	MP:0000702	enlarged lymph nodes	Serpinb10<em1(IMPC)Mbp>/Serpinb10<em1(IMPC)Mbp>	C57BL/6NCrl-Serpinb10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370433	F	MP:0000691	enlarged spleen	Serpinb10<em1(IMPC)Mbp>/Serpinb10<em1(IMPC)Mbp>	C57BL/6NCrl-Serpinb10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370433	M	MP:0000266	abnormal heart morphology	Serpinb10<em1(IMPC)Mbp>/Serpinb10<em1(IMPC)Mbp>	C57BL/6NCrl-Serpinb10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370433	F	MP:0004952	increased spleen weight	Serpinb10<em1(IMPC)Mbp>/Serpinb10<em1(IMPC)Mbp>	C57BL/6NCrl-Serpinb10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370433	F	MP:0001175	abnormal lung morphology	Serpinb10<em1(IMPC)Mbp>/Serpinb10<em1(IMPC)Mbp>	C57BL/6NCrl-Serpinb10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370433	F	MP:0002135	abnormal kidney morphology	Serpinb10<em1(IMPC)Mbp>/Serpinb10<em1(IMPC)Mbp>	C57BL/6NCrl-Serpinb10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370433	M	MP:0000195	decreased circulating calcium level	Serpinb10<em1(IMPC)Mbp>/Serpinb10<em1(IMPC)Mbp>	C57BL/6NCrl-Serpinb10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370433	M	MP:0001325	abnormal retina morphology	Serpinb10<em1(IMPC)Mbp>/Serpinb10<em1(IMPC)Mbp>	C57BL/6NCrl-Serpinb10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370433	F	MP:0000598	abnormal liver morphology	Serpinb10<em1(IMPC)Mbp>/Serpinb10<em1(IMPC)Mbp>	C57BL/6NCrl-Serpinb10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370433	M	MP:0000277	abnormal heart shape	Serpinb10<em1(IMPC)Mbp>/Serpinb10<em1(IMPC)Mbp>	C57BL/6NCrl-Serpinb10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370433	M	MP:0002644	decreased circulating triglyceride level	Serpinb10<em1(IMPC)Mbp>/Serpinb10<em1(IMPC)Mbp>	C57BL/6NCrl-Serpinb10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370433	F	MP:0002339	abnormal lymph node morphology	Serpinb10<em1(IMPC)Mbp>/Serpinb10<em1(IMPC)Mbp>	C57BL/6NCrl-Serpinb10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370436	M	MP:0020870	decreased thigmotaxis	Slc25a18<em1(IMPC)Mbp>/Slc25a18<em1(IMPC)Mbp>	C57BL/6NCrl-Slc25a18<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370436	M	MP:0002152	abnormal brain morphology	Slc25a18<em1(IMPC)Mbp>/Slc25a18<em1(IMPC)Mbp>	C57BL/6NCrl-Slc25a18<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370436	M	MP:0010024	increased total body fat amount	Slc25a18<em1(IMPC)Mbp>/Slc25a18<em1(IMPC)Mbp>	C57BL/6NCrl-Slc25a18<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370436	M	MP:0004931	enlarged epididymis	Slc25a18<em1(IMPC)Mbp>/Slc25a18<em1(IMPC)Mbp>	C57BL/6NCrl-Slc25a18<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370436	M	MP:0004924	abnormal behavior	Slc25a18<em1(IMPC)Mbp>/Slc25a18<em1(IMPC)Mbp>	C57BL/6NCrl-Slc25a18<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370436	M	MP:0002631	abnormal epididymis morphology	Slc25a18<em1(IMPC)Mbp>/Slc25a18<em1(IMPC)Mbp>	C57BL/6NCrl-Slc25a18<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370436	M	MP:0001364	decreased anxiety-related response	Slc25a18<em1(IMPC)Mbp>/Slc25a18<em1(IMPC)Mbp>	C57BL/6NCrl-Slc25a18<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370436	M	MP:0001891	hydrocephaly	Slc25a18<em1(IMPC)Mbp>/Slc25a18<em1(IMPC)Mbp>	C57BL/6NCrl-Slc25a18<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370437	M	MP:0001415	increased exploration in new environment	Srbd1<em1(IMPC)J>/Srbd1<+>	C57BL/6NJ-Srbd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370437	M	MP:0002075	abnormal coat/hair pigmentation	Srbd1<em1(IMPC)J>/Srbd1<+>	C57BL/6NJ-Srbd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370437	F	MP:0010052	increased grip strength	Srbd1<em1(IMPC)J>/Srbd1<+>	C57BL/6NJ-Srbd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370438	F	MP:0001566	increased circulating phosphate level	Stard9<em1(IMPC)J>/Stard9<em1(IMPC)J>	C57BL/6NJ-Stard9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370438	F	MP:0005553	increased circulating creatinine level	Stard9<em1(IMPC)J>/Stard9<em1(IMPC)J>	C57BL/6NJ-Stard9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370440	M	MP:0001289	persistence of hyaloid vascular system	Syde1<tm1b(EUCOMM)Hmgu>/Syde1<+>	C57BL/6N-Syde1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6370441	F	MP:0020870	decreased thigmotaxis	Tiprl<tm1.1(KOMP)Vlcg>/Tiprl<+>	C57BL/6N-Tiprl<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6370442	F	MP:0001399	hyperactivity	Tmem104<tm1.1(KOMP)Vlcg>/Tmem104<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem104<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6370442	F	MP:0002941	increased circulating alanine transaminase level	Tmem104<tm1.1(KOMP)Vlcg>/Tmem104<tm1.1(KOMP)Vlcg>	C57BL/6N-Tmem104<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6370443	F	MP:0001258	decreased body length	Tmem138<tm1b(EUCOMM)Wtsi>/Tmem138<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem138<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6370443	F	MP:0010124	decreased bone mineral content	Tmem138<tm1b(EUCOMM)Wtsi>/Tmem138<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem138<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6370443	M	MP:0004952	increased spleen weight	Tmem138<tm1b(EUCOMM)Wtsi>/Tmem138<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem138<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6370443	M	MP:0002953	thick ventricular wall	Tmem138<tm1b(EUCOMM)Wtsi>/Tmem138<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem138<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6370443	F	MP:0010053	decreased grip strength	Tmem138<tm1b(EUCOMM)Wtsi>/Tmem138<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem138<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6370443	F	MP:0009142	decreased prepulse inhibition	Tmem138<tm1b(EUCOMM)Wtsi>/Tmem138<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tmem138<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6370445	M	MP:0001513	limb grasping	Tnnc1<em1(IMPC)J>/Tnnc1<+>	C57BL/6NJ-Tnnc1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370445	M	MP:0001523	impaired righting response	Tnnc1<em1(IMPC)J>/Tnnc1<+>	C57BL/6NJ-Tnnc1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370446	F	MP:0000639	abnormal adrenal gland morphology	Trabd<em1(IMPC)Mbp>/Trabd<em1(IMPC)Mbp>	C57BL/6NCrl-Trabd<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370447	F	MP:0001364	decreased anxiety-related response	Trak2<em1(IMPC)Mbp>/Trak2<em1(IMPC)Mbp>	C57BL/6N-Trak2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6370447	M	MP:0002060	abnormal skin morphology	Trak2<em1(IMPC)Mbp>/Trak2<em1(IMPC)Mbp>	C57BL/6N-Trak2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6370447	F	MP:0004924	abnormal behavior	Trak2<em1(IMPC)Mbp>/Trak2<em1(IMPC)Mbp>	C57BL/6N-Trak2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6370447	F	MP:0000702	enlarged lymph nodes	Trak2<em1(IMPC)Mbp>/Trak2<em1(IMPC)Mbp>	C57BL/6N-Trak2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6370447	F	MP:0020870	decreased thigmotaxis	Trak2<em1(IMPC)Mbp>/Trak2<em1(IMPC)Mbp>	C57BL/6N-Trak2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6370447	F	MP:0002092	abnormal eye morphology	Trak2<em1(IMPC)Mbp>/Trak2<em1(IMPC)Mbp>	C57BL/6N-Trak2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6370447	F	MP:0002339	abnormal lymph node morphology	Trak2<em1(IMPC)Mbp>/Trak2<em1(IMPC)Mbp>	C57BL/6N-Trak2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6370447	F	MP:0001297	microphthalmia	Trak2<em1(IMPC)Mbp>/Trak2<em1(IMPC)Mbp>	C57BL/6N-Trak2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6370448	M	MP:0001304	cataract	Trav1<em1(IMPC)J>/Trav1<em1(IMPC)J>	C57BL/6NJ-Trav1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6370449	M	MP:0010052	increased grip strength	Ttll7<em1(IMPC)J>/Ttll7<em1(IMPC)J>	C57BL/6N-Ttll7<em1(IMPC)J>/J	N	MGI:5576271
MGI:6370451	F	MP:0002339	abnormal lymph node morphology	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	M	MP:0000538	abnormal urinary bladder morphology	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	M	MP:0002059	abnormal seminal vesicle morphology	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	M	MP:0000599	enlarged liver	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	M	MP:0001147	small testis	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	F	MP:0000702	enlarged lymph nodes	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	F	MP:0000691	enlarged spleen	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	M	MP:0002997	enlarged seminal vesicle	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	M	MP:0011874	enlarged urinary bladder	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	M	MP:0005419	decreased circulating serum albumin level	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	M	MP:0003642	absent seminal vesicle	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	M	MP:0002135	abnormal kidney morphology	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	F	MP:0000221	decreased leukocyte cell number	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	F	MP:0001325	abnormal retina morphology	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	F	MP:0002188	small heart	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	M	MP:0003068	enlarged kidney	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	M	MP:0001146	abnormal testis morphology	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370451	M	MP:0000598	abnormal liver morphology	Ubtf<em1(IMPC)Mbp>/Ubtf<+>	C57BL/6NCrl-Ubtf<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370452	F	MP:0010097	abnormal retina blood vessel morphology	Uroc1<em1(IMPC)Bay>/Uroc1<em1(IMPC)Bay>	C57BL/6N-Uroc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6370452	M	MP:0001417	decreased exploration in new environment	Uroc1<em1(IMPC)Bay>/Uroc1<em1(IMPC)Bay>	C57BL/6N-Uroc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6370455	F	MP:0001325	abnormal retina morphology	Ywhaq<em1(IMPC)J>/Ywhaq<em1(IMPC)J>	C57BL/6NJ-Ywhaq<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370456	F	MP:0002075	abnormal coat/hair pigmentation	Zc3h4<em1(IMPC)Mbp>/Zc3h4<+>	C57BL/6NCrl-Zc3h4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370456	F	MP:0002092	abnormal eye morphology	Zc3h4<em1(IMPC)Mbp>/Zc3h4<+>	C57BL/6NCrl-Zc3h4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370456	M	MP:0002631	abnormal epididymis morphology	Zc3h4<em1(IMPC)Mbp>/Zc3h4<+>	C57BL/6NCrl-Zc3h4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370456	M	MP:0004931	enlarged epididymis	Zc3h4<em1(IMPC)Mbp>/Zc3h4<+>	C57BL/6NCrl-Zc3h4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370457	M	MP:0004931	enlarged epididymis	Zfp398<em1(IMPC)Mbp>/Zfp398<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp398<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370457	M	MP:0000266	abnormal heart morphology	Zfp398<em1(IMPC)Mbp>/Zfp398<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp398<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370457	M	MP:0009477	small cecum	Zfp398<em1(IMPC)Mbp>/Zfp398<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp398<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370457	M	MP:0000274	enlarged heart	Zfp398<em1(IMPC)Mbp>/Zfp398<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp398<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370457	M	MP:0000494	abnormal cecum morphology	Zfp398<em1(IMPC)Mbp>/Zfp398<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp398<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370457	M	MP:0002833	increased heart weight	Zfp398<em1(IMPC)Mbp>/Zfp398<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp398<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370457	M	MP:0002631	abnormal epididymis morphology	Zfp398<em1(IMPC)Mbp>/Zfp398<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp398<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6370459	M	MP:0020870	decreased thigmotaxis	Zpld1<em1(IMPC)J>/Zpld1<em1(IMPC)J>	C57BL/6NJ-Zpld1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6370459	M	MP:0004924	abnormal behavior	Zpld1<em1(IMPC)J>/Zpld1<em1(IMPC)J>	C57BL/6NJ-Zpld1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6376290	F	MP:0013630	increased bone trabecular spacing	Gna11<em1Mman>/Gna11<em1Mman>	C57BL/6NCrl-Gna11<em1Mman>	N	28194446
MGI:6376290	F	MP:0000135	decreased compact bone thickness	Gna11<em1Mman>/Gna11<em1Mman>	C57BL/6NCrl-Gna11<em1Mman>	N	28194446
MGI:6376290	F	MP:0010869	decreased bone trabecula number	Gna11<em1Mman>/Gna11<em1Mman>	C57BL/6NCrl-Gna11<em1Mman>	N	28194446
MGI:6377057	M	MP:0009831	abnormal sperm midpiece morphology	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0020869	immotile sperm	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0009230	abnormal sperm head morphology	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0009838	abnormal sperm axoneme morphology	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0008898	abnormal acrosome morphology	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0004182	abnormal spermiation	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0008893	detached sperm flagellum	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0002687	oligozoospermia	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0005578	teratozoospermia	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0009239	short sperm flagellum	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0001932	abnormal spermiogenesis	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0006380	abnormal spermatid morphology	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0009238	coiled sperm flagellum	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0008892	abnormal sperm flagellum morphology	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0030590	abnormal sperm fibrous sheath morphology	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377057	M	MP:0001925	male infertility	Arl2bp<em1Visu>/Arl2bp<em1Visu>	involves: FVB/N	N	31425546
MGI:6377285	M	MP:0005452	abnormal adipose tissue amount	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0010378	increased respiratory quotient	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0010053	decreased grip strength	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0008489	slow postnatal weight gain	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0008963	increased carbon dioxide production	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0006038	increased mitochondrial fission	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0003440	decreased glycerol level	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0012106	impaired exercise endurance	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0005319	abnormal enzyme/coenzyme level	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0009403	increased variability of skeletal muscle fiber size	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0014174	decreased fatty acid beta-oxidation	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0030612	organic aciduria	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0003978	decreased circulating carnitine level	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0002106	abnormal muscle physiology	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0002702	decreased circulating free fatty acids level	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0001405	impaired coordination	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0010359	increased liver free fatty acids level	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0005281	increased fatty acids level	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0006036	abnormal mitochondrial physiology	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0031115	macrovesicular hepatic steatosis	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0005289	increased oxygen consumption	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0001764	abnormal homeostasis	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377285	M	MP:0013405	increased circulating lactate level	Adck2<tm1(KOMP)Vlcg>/Adck2<+>	C57BL/6-Adck2<tm1(KOMP)Vlcg>	N	31480808
MGI:6377564	M	MP:0009230	abnormal sperm head morphology	Ccdc63<em1Osb>/Ccdc63<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	26501274
MGI:6377564	M	MP:0001932	abnormal spermiogenesis	Ccdc63<em1Osb>/Ccdc63<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	26501274
MGI:6377564	M	MP:0008892	abnormal sperm flagellum morphology	Ccdc63<em1Osb>/Ccdc63<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	26501274
MGI:6377564	M	MP:0002675	asthenozoospermia	Ccdc63<em1Osb>/Ccdc63<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	26501274
MGI:6377564	M	MP:0009239	short sperm flagellum	Ccdc63<em1Osb>/Ccdc63<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	26501274
MGI:6377564	M	MP:0001925	male infertility	Ccdc63<em1Osb>/Ccdc63<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	26501274
MGI:6378558	M	MP:0002675	asthenozoospermia	Best1<tm2.1Web>/Best1<tm2.1Web>	involves: 129S1/Sv * CD-1	N	31201163
MGI:6378623	F	MP:0002135	abnormal kidney morphology	Col4a5<tm1Yseg>/Col4a5<+>,Lamb2<em1Jhm>/Lamb2<+>	involves: 129X1/SvJ * C57BL/6J * CBA/J	N	29263159
MGI:6378623	F	MP:0002871	albuminuria	Col4a5<tm1Yseg>/Col4a5<+>,Lamb2<em1Jhm>/Lamb2<+>	involves: 129X1/SvJ * C57BL/6J * CBA/J	N	29263159
MGI:6378623	F	MP:0005264	glomerulosclerosis	Col4a5<tm1Yseg>/Col4a5<+>,Lamb2<em1Jhm>/Lamb2<+>	involves: 129X1/SvJ * C57BL/6J * CBA/J	N	29263159
MGI:6378625	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Gt(ROSA)26Sor<tm1(CAG-PTPN1,-EGFP)Mtr>/Gt(ROSA)26Sor<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	27020859
MGI:6378625	M	MP:0005305	prostate gland anterior lobe hyperplasia	Gt(ROSA)26Sor<tm1(CAG-PTPN1,-EGFP)Mtr>/Gt(ROSA)26Sor<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	N	27020859
MGI:6378626	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Ptpn1<tm1Bpk>/Ptpn1<tm1Bpk>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	27020859
MGI:6378626	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Ptpn1<tm1Bpk>/Ptpn1<tm1Bpk>,Tg(Pbsn-cre)4Prb/0	involves: 129S4/SvJae * C57BL/6 * DBA/2	N	27020859
MGI:6379006	M	MP:0001441	increased grooming behavior	Shank3<tm1.1Cya>/Shank3<tm1.1Cya>	B6.Cg-Shank3<tm1.1Cya>	N	31275112
MGI:6379006	M	MP:0002272	abnormal nervous system electrophysiology	Shank3<tm1.1Cya>/Shank3<tm1.1Cya>	B6.Cg-Shank3<tm1.1Cya>	N	31275112
MGI:6379006	M	MP:0003908	decreased stereotypic behavior	Shank3<tm1.1Cya>/Shank3<tm1.1Cya>	B6.Cg-Shank3<tm1.1Cya>	N	31275112
MGI:6379006	M	MP:0001363	increased anxiety-related response	Shank3<tm1.1Cya>/Shank3<tm1.1Cya>	B6.Cg-Shank3<tm1.1Cya>	N	31275112
MGI:6379006	F	MP:0014382	increased miniature inhibitory postsynaptic current frequency	Shank3<tm1.1Cya>/Shank3<tm1.1Cya>	B6.Cg-Shank3<tm1.1Cya>	N	31275112
MGI:6379006	M	MP:0002887	decreased susceptibility to pharmacologically induced seizures	Shank3<tm1.1Cya>/Shank3<tm1.1Cya>	B6.Cg-Shank3<tm1.1Cya>	N	31275112
MGI:6379006	M	MP:0004811	abnormal neuron physiology	Shank3<tm1.1Cya>/Shank3<tm1.1Cya>	B6.Cg-Shank3<tm1.1Cya>	N	31275112
MGI:6379006	M	MP:0004994	abnormal brain wave pattern	Shank3<tm1.1Cya>/Shank3<tm1.1Cya>	B6.Cg-Shank3<tm1.1Cya>	N	31275112
MGI:6379011	M	MP:0005386	behavior/neurological phenotype	Shank3<tm1.1Cya>/Shank3<+>	B6.Cg-Shank3<tm1.1Cya>	Y	31275112
MGI:6379011	M	MP:0001441	increased grooming behavior	Shank3<tm1.1Cya>/Shank3<+>	B6.Cg-Shank3<tm1.1Cya>	N	31275112
MGI:6379011	M	MP:0001529	abnormal vocalization	Shank3<tm1.1Cya>/Shank3<+>	B6.Cg-Shank3<tm1.1Cya>	N	31275112
MGI:6379011	M	MP:0001363	increased anxiety-related response	Shank3<tm1.1Cya>/Shank3<+>	B6.Cg-Shank3<tm1.1Cya>	N	31275112
MGI:6379011	M	MP:0003908	decreased stereotypic behavior	Shank3<tm1.1Cya>/Shank3<+>	B6.Cg-Shank3<tm1.1Cya>	N	31275112
MGI:6379024	M	MP:0008873	increased physiological sensitivity to xenobiotic	Cyb5r3<tm1c(KOMP)Wtsi>/Cyb5r3<tm1c(KOMP)Wtsi>,X/Tg(Myh11-icre/ERT2)1Soff	B6.Cg-Cyb5r3<tm1c(KOMP)Wtsi> Tg(Myh11-icre/ERT2)1Soff	N	31487266
MGI:6379024	M	MP:0012045	increased susceptibility to hypertension	Cyb5r3<tm1c(KOMP)Wtsi>/Cyb5r3<tm1c(KOMP)Wtsi>,X/Tg(Myh11-icre/ERT2)1Soff	B6.Cg-Cyb5r3<tm1c(KOMP)Wtsi> Tg(Myh11-icre/ERT2)1Soff	N	31487266
MGI:6379024	M	MP:0000223	decreased monocyte cell number	Cyb5r3<tm1c(KOMP)Wtsi>/Cyb5r3<tm1c(KOMP)Wtsi>,X/Tg(Myh11-icre/ERT2)1Soff	B6.Cg-Cyb5r3<tm1c(KOMP)Wtsi> Tg(Myh11-icre/ERT2)1Soff	N	31487266
MGI:6379024	M	MP:0003025	increased vasoconstriction	Cyb5r3<tm1c(KOMP)Wtsi>/Cyb5r3<tm1c(KOMP)Wtsi>,X/Tg(Myh11-icre/ERT2)1Soff	B6.Cg-Cyb5r3<tm1c(KOMP)Wtsi> Tg(Myh11-icre/ERT2)1Soff	N	31487266
MGI:6379024	M	MP:0004875	increased mean systemic arterial blood pressure	Cyb5r3<tm1c(KOMP)Wtsi>/Cyb5r3<tm1c(KOMP)Wtsi>,X/Tg(Myh11-icre/ERT2)1Soff	B6.Cg-Cyb5r3<tm1c(KOMP)Wtsi> Tg(Myh11-icre/ERT2)1Soff	N	31487266
MGI:6379024	M	MP:0005333	decreased heart rate	Cyb5r3<tm1c(KOMP)Wtsi>/Cyb5r3<tm1c(KOMP)Wtsi>,X/Tg(Myh11-icre/ERT2)1Soff	B6.Cg-Cyb5r3<tm1c(KOMP)Wtsi> Tg(Myh11-icre/ERT2)1Soff	N	31487266
MGI:6379024	M	MP:0005590	increased vasodilation	Cyb5r3<tm1c(KOMP)Wtsi>/Cyb5r3<tm1c(KOMP)Wtsi>,X/Tg(Myh11-icre/ERT2)1Soff	B6.Cg-Cyb5r3<tm1c(KOMP)Wtsi> Tg(Myh11-icre/ERT2)1Soff	N	31487266
MGI:6379024	M	MP:0005591	decreased vasodilation	Cyb5r3<tm1c(KOMP)Wtsi>/Cyb5r3<tm1c(KOMP)Wtsi>,X/Tg(Myh11-icre/ERT2)1Soff	B6.Cg-Cyb5r3<tm1c(KOMP)Wtsi> Tg(Myh11-icre/ERT2)1Soff	N	31487266
MGI:6379310	M	MP:0005389	reproductive system phenotype	X/Ddx3y<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	30613052
MGI:6379312	M	MP:0013293	embryonic lethality prior to tooth bud stage	Ddx3x<em1Osb>/Y,X/Ddx3y<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30613052
MGI:6379312	M	MP:0001698	decreased embryo size	Ddx3x<em1Osb>/Y,X/Ddx3y<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	30613052
MGI:6379314	M	MP:0005389	reproductive system phenotype	Ddx3x<em2Osb>/Y,X/Ddx3y<em1Osb>	chimera involves: 129S2/SvPas * C57BL/6NSlc	Y	30613052
MGI:6379568	F	MP:0003718	maternal effect	Rasa3<scat>/Rasa3<+>	involves: BALB/cBy	N	8334700
MGI:6379580	M	MP:0006380	abnormal spermatid morphology	Ddias<tm1Enik>/Ddias<tm1Enik>	Not Specified	N	17515607
MGI:6379580	M	MP:0004901	decreased male germ cell number	Ddias<tm1Enik>/Ddias<tm1Enik>	Not Specified	N	17515607
MGI:6379588	M	MP:0004924	abnormal behavior	Fpr3<tm1b(EUCOMM)Hmgu>/Fpr3<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N	N	31653840
MGI:6379623	M	MP:0030941	enhanced autophagy	Tg(Myl1-Trp53inp2)2Azo/0	involves: C57BL/6J	N	24713655
MGI:6380702	F	MP:0005389	reproductive system phenotype	Ywhah<tm1.1Cya>/Ywhah<tm1.1Cya>,Tg(Zp3-cre)93Knw/0	C57BL/6-Ywhah<tm1.1Cya> Tg(Zp3-cre)93Knw	Y	31640562
MGI:6380703	F	MP:0005389	reproductive system phenotype	Ywhah<tm1.2Cya>/Ywhah<tm1.2Cya>	involves: C57BL/6N * FVB	Y	31640562
MGI:6380704	F	MP:0005389	reproductive system phenotype	Ywhae<tm2.1Awb>/Ywhae<tm2.1Awb>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6J	Y	31640562
MGI:6380705	F	MP:0001926	female infertility	Ywhae<tm2.2Awb>/Ywhae<tm2.2Awb>	involves: C57BL/6N * FVB	N	31640562
MGI:6382908	F	MP:0002083	premature death	Sirt6<tm1Fwa>/Sirt6<tm1Fwa>	involves: 129S6/SvEvTac * BALB/cJ	N	28448551
MGI:6382908	F	MP:0002727	decreased circulating insulin level	Sirt6<tm1Fwa>/Sirt6<tm1Fwa>	involves: 129S6/SvEvTac * BALB/cJ	N	28448551
MGI:6382908	M	MP:0002083	premature death	Sirt6<tm1Fwa>/Sirt6<tm1Fwa>	involves: 129S6/SvEvTac * BALB/cJ	N	28448551
MGI:6382908	M	MP:0002727	decreased circulating insulin level	Sirt6<tm1Fwa>/Sirt6<tm1Fwa>	involves: 129S6/SvEvTac * BALB/cJ	N	28448551
MGI:6382908	M	MP:0008844	decreased subcutaneous adipose tissue amount	Sirt6<tm1Fwa>/Sirt6<tm1Fwa>	involves: 129S6/SvEvTac * BALB/cJ	N	28448551
MGI:6382992	F	MP:0001926	female infertility	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	F	MP:0005584	abnormal enzyme/coenzyme activity	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	M	MP:0006380	abnormal spermatid morphology	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	M	MP:0005584	abnormal enzyme/coenzyme activity	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	M	MP:0008261	arrest of male meiosis	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	F	MP:0001927	abnormal estrous cycle	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	F	MP:0011128	increased tertiary ovarian follicle number	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	F	MP:0003355	decreased ovulation rate	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	M	MP:0001925	male infertility	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	F	MP:0009011	prolonged diestrus	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	M	MP:0006379	abnormal spermatocyte morphology	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	M	MP:0006319	abnormal epididymal fat pad morphology	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	M	MP:0001751	increased circulating luteinizing hormone level	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	M	MP:0001156	abnormal spermatogenesis	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6382992	M	MP:0001750	increased circulating follicle stimulating hormone level	Agpat1<tm1Garg>/Agpat1<tm1Garg>	involves: 129S6/SvEvTac * C57BL/6	N	28973305
MGI:6383181	M	MP:0002687	oligozoospermia	Gpx4<tm1Yana>/Gpx4<tm1Yana>,Tg(Gpx4)#Yana/0,Tg(Pgk2-cre)24Shb/0	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2 * ICR	N	19783653
MGI:6383181	M	MP:0004852	decreased testis weight	Gpx4<tm1Yana>/Gpx4<tm1Yana>,Tg(Gpx4)#Yana/0,Tg(Pgk2-cre)24Shb/0	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2 * ICR	N	19783653
MGI:6383181	M	MP:0014465	abnormal sperm mitochondrial morphology	Gpx4<tm1Yana>/Gpx4<tm1Yana>,Tg(Gpx4)#Yana/0,Tg(Pgk2-cre)24Shb/0	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2 * ICR	N	19783653
MGI:6383181	M	MP:0006362	abnormal male germ cell morphology	Gpx4<tm1Yana>/Gpx4<tm1Yana>,Tg(Gpx4)#Yana/0,Tg(Pgk2-cre)24Shb/0	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2 * ICR	N	19783653
MGI:6383181	M	MP:0011635	abnormal mitochondrial crista morphology	Gpx4<tm1Yana>/Gpx4<tm1Yana>,Tg(Gpx4)#Yana/0,Tg(Pgk2-cre)24Shb/0	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2 * ICR	N	19783653
MGI:6383181	M	MP:0004901	decreased male germ cell number	Gpx4<tm1Yana>/Gpx4<tm1Yana>,Tg(Gpx4)#Yana/0,Tg(Pgk2-cre)24Shb/0	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2 * ICR	N	19783653
MGI:6383181	M	MP:0009243	hairpin sperm flagellum	Gpx4<tm1Yana>/Gpx4<tm1Yana>,Tg(Gpx4)#Yana/0,Tg(Pgk2-cre)24Shb/0	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2 * ICR	N	19783653
MGI:6383181	M	MP:0001925	male infertility	Gpx4<tm1Yana>/Gpx4<tm1Yana>,Tg(Gpx4)#Yana/0,Tg(Pgk2-cre)24Shb/0	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2 * ICR	N	19783653
MGI:6383181	M	MP:0006036	abnormal mitochondrial physiology	Gpx4<tm1Yana>/Gpx4<tm1Yana>,Tg(Gpx4)#Yana/0,Tg(Pgk2-cre)24Shb/0	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2 * ICR	N	19783653
MGI:6383181	M	MP:0004543	abnormal sperm physiology	Gpx4<tm1Yana>/Gpx4<tm1Yana>,Tg(Gpx4)#Yana/0,Tg(Pgk2-cre)24Shb/0	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2 * ICR	N	19783653
MGI:6383181	M	MP:0002675	asthenozoospermia	Gpx4<tm1Yana>/Gpx4<tm1Yana>,Tg(Gpx4)#Yana/0,Tg(Pgk2-cre)24Shb/0	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2 * ICR	N	19783653
MGI:6383181	M	MP:0001147	small testis	Gpx4<tm1Yana>/Gpx4<tm1Yana>,Tg(Gpx4)#Yana/0,Tg(Pgk2-cre)24Shb/0	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2 * ICR	N	19783653
MGI:6383471	M	MP:0008516	disorganized retina outer nuclear layer	Rs1<em1Fegu>/Y	involves: C57BL/6J	N	29379415
MGI:6383471	M	MP:0008582	short photoreceptor inner segment	Rs1<em1Fegu>/Y	involves: C57BL/6J	N	29379415
MGI:6383471	M	MP:0001004	abnormal retina photoreceptor morphology	Rs1<em1Fegu>/Y	involves: C57BL/6J	N	29379415
MGI:6383471	M	MP:0020816	decreased photoreceptor outer segment number	Rs1<em1Fegu>/Y	involves: C57BL/6J	N	29379415
MGI:6383471	M	MP:0008580	photoreceptor inner segment degeneration	Rs1<em1Fegu>/Y	involves: C57BL/6J	N	29379415
MGI:6383471	M	MP:0005551	abnormal eye electrophysiology	Rs1<em1Fegu>/Y	involves: C57BL/6J	N	29379415
MGI:6383471	M	MP:0012144	decreased b-wave amplitude	Rs1<em1Fegu>/Y	involves: C57BL/6J	N	29379415
MGI:6383471	M	MP:0008512	disorganized retina inner nuclear layer	Rs1<em1Fegu>/Y	involves: C57BL/6J	N	29379415
MGI:6383471	M	MP:0008515	thin retina outer nuclear layer	Rs1<em1Fegu>/Y	involves: C57BL/6J	N	29379415
MGI:6383471	M	MP:0006069	abnormal retina neuronal layer morphology	Rs1<em1Fegu>/Y	involves: C57BL/6J	N	29379415
MGI:6383471	M	MP:0003732	abnormal retina outer plexiform layer morphology	Rs1<em1Fegu>/Y	involves: C57BL/6J	N	29379415
MGI:6383471	M	MP:0008520	disorganized retina outer plexiform layer	Rs1<em1Fegu>/Y	involves: C57BL/6J	N	29379415
MGI:6383471	M	MP:0001325	abnormal retina morphology	Rs1<em1Fegu>/Y	involves: C57BL/6J	N	29379415
MGI:6383672	F	MP:0005121	decreased circulating prolactin level	7630403G23Rik<Tg(Th-cre)1Tmd>/7630403G23Rik<+>,Trpc5<tm1.1Mfre>/Trpc5<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N * SJL	N	31285329
MGI:6383672	F	MP:0005402	abnormal action potential	7630403G23Rik<Tg(Th-cre)1Tmd>/7630403G23Rik<+>,Trpc5<tm1.1Mfre>/Trpc5<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N * SJL	N	31285329
MGI:6383672	F	MP:0009011	prolonged diestrus	7630403G23Rik<Tg(Th-cre)1Tmd>/7630403G23Rik<+>,Trpc5<tm1.1Mfre>/Trpc5<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N * SJL	N	31285329
MGI:6383672	F	MP:0009016	abnormal estrus	7630403G23Rik<Tg(Th-cre)1Tmd>/7630403G23Rik<+>,Trpc5<tm1.1Mfre>/Trpc5<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N * SJL	N	31285329
MGI:6383672	F	MP:0001935	decreased litter size	7630403G23Rik<Tg(Th-cre)1Tmd>/7630403G23Rik<+>,Trpc5<tm1.1Mfre>/Trpc5<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N * SJL	N	31285329
MGI:6383672	F	MP:0002773	decreased circulating luteinizing hormone level	7630403G23Rik<Tg(Th-cre)1Tmd>/7630403G23Rik<+>,Trpc5<tm1.1Mfre>/Trpc5<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N * SJL	N	31285329
MGI:6383672	F	MP:0001923	reduced female fertility	7630403G23Rik<Tg(Th-cre)1Tmd>/7630403G23Rik<+>,Trpc5<tm1.1Mfre>/Trpc5<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N * SJL	N	31285329
MGI:6383672	F	MP:0009006	prolonged estrous cycle	7630403G23Rik<Tg(Th-cre)1Tmd>/7630403G23Rik<+>,Trpc5<tm1.1Mfre>/Trpc5<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N * SJL	N	31285329
MGI:6383672	F	MP:0003355	decreased ovulation rate	7630403G23Rik<Tg(Th-cre)1Tmd>/7630403G23Rik<+>,Trpc5<tm1.1Mfre>/Trpc5<tm1.1Mfre>	involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N * SJL	N	31285329
MGI:6383674	F	MP:0001923	reduced female fertility	Trpc5<tm1.2Mfre>/Trpc5<tm1.2Mfre>	B6N.129-Trpc5<tm1.2Mfre>	N	31285329
MGI:6383674	F	MP:0001935	decreased litter size	Trpc5<tm1.2Mfre>/Trpc5<tm1.2Mfre>	B6N.129-Trpc5<tm1.2Mfre>	N	31285329
MGI:6383674	F	MP:0005121	decreased circulating prolactin level	Trpc5<tm1.2Mfre>/Trpc5<tm1.2Mfre>	B6N.129-Trpc5<tm1.2Mfre>	N	31285329
MGI:6383674	F	MP:0009006	prolonged estrous cycle	Trpc5<tm1.2Mfre>/Trpc5<tm1.2Mfre>	B6N.129-Trpc5<tm1.2Mfre>	N	31285329
MGI:6383674	F	MP:0005402	abnormal action potential	Trpc5<tm1.2Mfre>/Trpc5<tm1.2Mfre>	B6N.129-Trpc5<tm1.2Mfre>	N	31285329
MGI:6384259	F	MP:0003699	abnormal female reproductive system physiology	Chaserr<em1Wei>/Chaserr<+>	involves: BALB/c * C57BL/6	N	31704914
MGI:6384263	F	MP:0003699	abnormal female reproductive system physiology	Chaserr<em2Wei>/Chaserr<+>	involves: BALB/c * C57BL/6	N	31704914
MGI:6384648	F	MP:0003718	maternal effect	Plgrkt<tm1Lmls>/Plgrkt<tm1Lmls>	B6.Cg-Plgrkt<tm1Lmls>	N	27714956
MGI:6384648	F	MP:0001262	decreased body weight	Plgrkt<tm1Lmls>/Plgrkt<tm1Lmls>	B6.Cg-Plgrkt<tm1Lmls>	N	27714956
MGI:6384648	F	MP:0013716	hypolactation	Plgrkt<tm1Lmls>/Plgrkt<tm1Lmls>	B6.Cg-Plgrkt<tm1Lmls>	N	27714956
MGI:6385202	M	MP:0005386	behavior/neurological phenotype	Wdr45<tm1Beij>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	Y	26000824
MGI:6385202	M	MP:0001405	impaired coordination	Wdr45<tm1Beij>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385202	M	MP:0008025	brain vacuoles	Wdr45<tm1Beij>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385202	M	MP:0008428	abnormal spatial working memory	Wdr45<tm1Beij>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385202	M	MP:0010047	axonal spheroids	Wdr45<tm1Beij>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385202	M	MP:0005405	axon degeneration	Wdr45<tm1Beij>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385202	M	MP:0000921	demyelination	Wdr45<tm1Beij>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385202	M	MP:0003354	astrocytosis	Wdr45<tm1Beij>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385202	M	MP:0030940	impaired autophagy	Wdr45<tm1Beij>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385202	M	MP:0002912	abnormal excitatory postsynaptic potential	Wdr45<tm1Beij>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385202	M	MP:0009454	impaired contextual conditioning behavior	Wdr45<tm1Beij>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385202	M	MP:0012307	impaired spatial learning	Wdr45<tm1Beij>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385202	M	MP:0001473	reduced long-term potentiation	Wdr45<tm1Beij>/Y,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385203	F	MP:0030940	impaired autophagy	Wdr45<tm1Beij>/Wdr45<tm1Beij>,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385203	F	MP:0010047	axonal spheroids	Wdr45<tm1Beij>/Wdr45<tm1Beij>,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385204	F	MP:0030940	impaired autophagy	Wdr45<tm1Beij>/Wdr45<+>,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385204	F	MP:0010047	axonal spheroids	Wdr45<tm1Beij>/Wdr45<+>,Tg(Nes-cre)1Kln/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL	N	26000824
MGI:6385859	M	MP:0006036	abnormal mitochondrial physiology	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6385859	M	MP:0003141	cardiac fibrosis	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6385859	M	MP:0012688	abnormal heart ventricles weight	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6385859	M	MP:0006138	congestive heart failure	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6385859	M	MP:0003674	oxidative stress	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6385859	M	MP:0002083	premature death	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6385859	M	MP:0011925	abnormal heart echocardiography feature	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6385859	M	MP:0005630	increased lung weight	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6385859	M	MP:0031633	decreased heart left ventricle muscle contractility	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6385859	M	MP:0000280	thin ventricular wall	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6385859	M	MP:0000274	enlarged heart	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6385859	M	MP:0002795	dilated cardiomyopathy	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6385859	M	MP:0008022	dilated heart ventricle	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6385859	M	MP:0001544	abnormal cardiovascular system physiology	Hspd1<tm1c(EUCOMM)Hmgu>/Hspd1<tm1c(EUCOMM)Hmgu>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N	N	31209364
MGI:6388550	M	MP:0001441	increased grooming behavior	Tbr1<tm1.1Csbd>/Tbr1<+>	involves: C57BL/6J	N	31680851
MGI:6388550	M	MP:0031391	increased locomotor activity	Tbr1<tm1.1Csbd>/Tbr1<+>	involves: C57BL/6J	N	31680851
MGI:6388550	M	MP:0002557	abnormal social/conspecific interaction behavior	Tbr1<tm1.1Csbd>/Tbr1<+>	involves: C57BL/6J	N	31680851
MGI:6388550	M	MP:0011620	abnormal habituation to a new environment	Tbr1<tm1.1Csbd>/Tbr1<+>	involves: C57BL/6J	N	31680851
MGI:6388550	M	MP:0001363	increased anxiety-related response	Tbr1<tm1.1Csbd>/Tbr1<+>	involves: C57BL/6J	N	31680851
MGI:6388550	M	MP:0002574	increased vertical activity	Tbr1<tm1.1Csbd>/Tbr1<+>	involves: C57BL/6J	N	31680851
MGI:6388550	M	MP:0020870	decreased thigmotaxis	Tbr1<tm1.1Csbd>/Tbr1<+>	involves: C57BL/6J	N	31680851
MGI:6388658	F	MP:0009050	dilated proximal convoluted tubule	Pkhd1<em1Mrug>/Pkhd1<+>	involves: C57BL/6J	N	30600684
MGI:6388658	F	MP:0000521	abnormal kidney cortex morphology	Pkhd1<em1Mrug>/Pkhd1<+>	involves: C57BL/6J	N	30600684
MGI:6388658	F	MP:0002135	abnormal kidney morphology	Pkhd1<em1Mrug>/Pkhd1<+>	involves: C57BL/6J	N	30600684
MGI:6388659	F	MP:0009050	dilated proximal convoluted tubule	Pkhd1<em1Mrug>/Pkhd1<em1Mrug>	involves: C57BL/6J	N	30600684
MGI:6388659	F	MP:0002135	abnormal kidney morphology	Pkhd1<em1Mrug>/Pkhd1<em1Mrug>	involves: C57BL/6J	N	30600684
MGI:6388692	M	MP:0001925	male infertility	Jam3<tm1Lex>/Jam3<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	19109565
MGI:6388692	M	MP:0005159	azoospermia	Jam3<tm1Lex>/Jam3<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	N	19109565
MGI:6389564	M	MP:0001930	abnormal meiosis	Hells<tm1c(EUCOMM)Wtsi>/Hells<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	(B6(Cg)-Hells<tm1c(EUCOMM)Wtsi>/BakrJ x B6.Cg-Hells<tm1d(EUCOMM)Wtsi> Tg(Stra8-icre)1Reb/Bakr)F1	N	32001511
MGI:6389564	M	MP:0004852	decreased testis weight	Hells<tm1c(EUCOMM)Wtsi>/Hells<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	(B6(Cg)-Hells<tm1c(EUCOMM)Wtsi>/BakrJ x B6.Cg-Hells<tm1d(EUCOMM)Wtsi> Tg(Stra8-icre)1Reb/Bakr)F1	N	32001511
MGI:6389564	M	MP:0008261	arrest of male meiosis	Hells<tm1c(EUCOMM)Wtsi>/Hells<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	(B6(Cg)-Hells<tm1c(EUCOMM)Wtsi>/BakrJ x B6.Cg-Hells<tm1d(EUCOMM)Wtsi> Tg(Stra8-icre)1Reb/Bakr)F1	N	32001511
MGI:6389564	M	MP:0008878	abnormal DNA methylation during gametogenesis	Hells<tm1c(EUCOMM)Wtsi>/Hells<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	(B6(Cg)-Hells<tm1c(EUCOMM)Wtsi>/BakrJ x B6.Cg-Hells<tm1d(EUCOMM)Wtsi> Tg(Stra8-icre)1Reb/Bakr)F1	N	32001511
MGI:6389564	M	MP:0001925	male infertility	Hells<tm1c(EUCOMM)Wtsi>/Hells<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	(B6(Cg)-Hells<tm1c(EUCOMM)Wtsi>/BakrJ x B6.Cg-Hells<tm1d(EUCOMM)Wtsi> Tg(Stra8-icre)1Reb/Bakr)F1	N	32001511
MGI:6389564	M	MP:0008877	abnormal DNA methylation	Hells<tm1c(EUCOMM)Wtsi>/Hells<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	(B6(Cg)-Hells<tm1c(EUCOMM)Wtsi>/BakrJ x B6.Cg-Hells<tm1d(EUCOMM)Wtsi> Tg(Stra8-icre)1Reb/Bakr)F1	N	32001511
MGI:6389564	M	MP:0004901	decreased male germ cell number	Hells<tm1c(EUCOMM)Wtsi>/Hells<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	(B6(Cg)-Hells<tm1c(EUCOMM)Wtsi>/BakrJ x B6.Cg-Hells<tm1d(EUCOMM)Wtsi> Tg(Stra8-icre)1Reb/Bakr)F1	N	32001511
MGI:6389564	M	MP:0014052	increased male germ cell apoptosis	Hells<tm1c(EUCOMM)Wtsi>/Hells<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	(B6(Cg)-Hells<tm1c(EUCOMM)Wtsi>/BakrJ x B6.Cg-Hells<tm1d(EUCOMM)Wtsi> Tg(Stra8-icre)1Reb/Bakr)F1	N	32001511
MGI:6390550	M	MP:0005376	homeostasis/metabolism phenotype	Selenow<em#Hwl>/Selenow<em#Hwl>	C57BL/6-Selenow<em#Hwl>	Y	31509445
MGI:6390889	M	MP:0001552	increased circulating triglyceride level	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0001554	increased circulating free fatty acids level	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0000186	decreased circulating HDL cholesterol level	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	F	MP:0005378	growth/size/body region phenotype	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	Y	31439668
MGI:6390889	M	MP:0000183	decreased circulating LDL cholesterol level	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0000609	abnormal liver physiology	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0003443	increased circulating glycerol level	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0004777	abnormal phospholipid level	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0001262	decreased body weight	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0008963	increased carbon dioxide production	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0008965	increased basal metabolism	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0000601	small liver	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0014143	decreased body fat mass	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0005179	decreased circulating cholesterol level	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0003975	increased circulating VLDL triglyceride level	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0010379	decreased respiratory quotient	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0003961	decreased lean body mass	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0003983	decreased cholesterol level	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0010026	decreased liver cholesterol level	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0005145	increased circulating VLDL cholesterol level	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0001783	decreased white adipose tissue amount	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0009293	decreased inguinal fat pad weight	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0009356	decreased liver triglyceride level	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0005376	homeostasis/metabolism phenotype	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	Y	31439668
MGI:6390889	M	MP:0005289	increased oxygen consumption	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0008034	enhanced lipolysis	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0004889	increased energy expenditure	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390889	M	MP:0009289	decreased epididymal fat pad weight	C1qtnf2<tm1Lex>/C1qtnf2<tm1Lex>	B6.129S5-C1qtnf2<tm1Lex>	N	31439668
MGI:6390918	M	MP:0002797	increased thigmotaxis	Chd8<tm1.1Csbd>/Chd8<+>	involves: C57BL/6J	N	30104731
MGI:6390918	F	MP:0002152	abnormal brain morphology	Chd8<tm1.1Csbd>/Chd8<+>	involves: C57BL/6J	N	30104731
MGI:6390918	M	MP:0013140	excessive vocalization	Chd8<tm1.1Csbd>/Chd8<+>	involves: C57BL/6J	N	30104731
MGI:6390918	M	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude	Chd8<tm1.1Csbd>/Chd8<+>	involves: C57BL/6J	N	30104731
MGI:6390918	M	MP:0001402	decreased locomotor activity	Chd8<tm1.1Csbd>/Chd8<+>	involves: C57BL/6J	N	30104731
MGI:6390918	F	MP:0014382	increased miniature inhibitory postsynaptic current frequency	Chd8<tm1.1Csbd>/Chd8<+>	involves: C57BL/6J	N	30104731
MGI:6390918	M	MP:0014383	decreased miniature inhibitory postsynaptic current frequency	Chd8<tm1.1Csbd>/Chd8<+>	involves: C57BL/6J	N	30104731
MGI:6390918	M	MP:0002557	abnormal social/conspecific interaction behavior	Chd8<tm1.1Csbd>/Chd8<+>	involves: C57BL/6J	N	30104731
MGI:6390918	M	MP:0001441	increased grooming behavior	Chd8<tm1.1Csbd>/Chd8<+>	involves: C57BL/6J	N	30104731
MGI:6391118	M	MP:0009243	hairpin sperm flagellum	Ttc29<em1Fzh>/Ttc29<em1Fzh>	involves: C57BL/6	N	31735294
MGI:6391118	M	MP:0001922	reduced male fertility	Ttc29<em1Fzh>/Ttc29<em1Fzh>	involves: C57BL/6	N	31735294
MGI:6391118	M	MP:0009836	abnormal sperm principal piece morphology	Ttc29<em1Fzh>/Ttc29<em1Fzh>	involves: C57BL/6	N	31735294
MGI:6391118	M	MP:0020451	decreased sperm progressive motility	Ttc29<em1Fzh>/Ttc29<em1Fzh>	involves: C57BL/6	N	31735294
MGI:6391118	M	MP:0009831	abnormal sperm midpiece morphology	Ttc29<em1Fzh>/Ttc29<em1Fzh>	involves: C57BL/6	N	31735294
MGI:6391118	M	MP:0009837	abnormal sperm end piece morphology	Ttc29<em1Fzh>/Ttc29<em1Fzh>	involves: C57BL/6	N	31735294
MGI:6391118	M	MP:0002675	asthenozoospermia	Ttc29<em1Fzh>/Ttc29<em1Fzh>	involves: C57BL/6	N	31735294
MGI:6391118	M	MP:0005389	reproductive system phenotype	Ttc29<em1Fzh>/Ttc29<em1Fzh>	involves: C57BL/6	Y	31735294
MGI:6392160	F	MP:0020082	increased hippocampus volume	Iqsec2<em1Csbg>/Iqsec2<+>	C57BL/6NHsd-Iqsec2<em1Csbg>	N	31439632
MGI:6392160	F	MP:0004996	abnormal CNS synapse formation	Iqsec2<em1Csbg>/Iqsec2<+>	C57BL/6NHsd-Iqsec2<em1Csbg>	N	31439632
MGI:6392160	F	MP:0001361	social withdrawal	Iqsec2<em1Csbg>/Iqsec2<+>	C57BL/6NHsd-Iqsec2<em1Csbg>	N	31439632
MGI:6392160	F	MP:0000951	sporadic seizures	Iqsec2<em1Csbg>/Iqsec2<+>	C57BL/6NHsd-Iqsec2<em1Csbg>	N	31439632
MGI:6392160	F	MP:0010053	decreased grip strength	Iqsec2<em1Csbg>/Iqsec2<+>	C57BL/6NHsd-Iqsec2<em1Csbg>	N	31439632
MGI:6392160	F	MP:0012307	impaired spatial learning	Iqsec2<em1Csbg>/Iqsec2<+>	C57BL/6NHsd-Iqsec2<em1Csbg>	N	31439632
MGI:6392160	F	MP:0002566	abnormal sexual interaction	Iqsec2<em1Csbg>/Iqsec2<+>	C57BL/6NHsd-Iqsec2<em1Csbg>	N	31439632
MGI:6392160	F	MP:0001415	increased exploration in new environment	Iqsec2<em1Csbg>/Iqsec2<+>	C57BL/6NHsd-Iqsec2<em1Csbg>	N	31439632
MGI:6392160	F	MP:0020573	abnormal corpus callosum size	Iqsec2<em1Csbg>/Iqsec2<+>	C57BL/6NHsd-Iqsec2<em1Csbg>	N	31439632
MGI:6392160	F	MP:0012459	increased dentate gyrus size	Iqsec2<em1Csbg>/Iqsec2<+>	C57BL/6NHsd-Iqsec2<em1Csbg>	N	31439632
MGI:6392160	F	MP:0008428	abnormal spatial working memory	Iqsec2<em1Csbg>/Iqsec2<+>	C57BL/6NHsd-Iqsec2<em1Csbg>	N	31439632
MGI:6392160	F	MP:0031391	increased locomotor activity	Iqsec2<em1Csbg>/Iqsec2<+>	C57BL/6NHsd-Iqsec2<em1Csbg>	N	31439632
MGI:6392161	M	MP:0000951	sporadic seizures	Iqsec2<em1Csbg>/Y	C57BL/6NHsd-Iqsec2<em1Csbg>	N	31439632
MGI:6392615	M	MP:0012348	decreased susceptibility to induction of seizure by inducing agent	Iqsec2<em1Frk>/Y	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6392615	M	MP:0011987	abnormal GABAergic neuron physiology	Iqsec2<em1Frk>/Y	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6392615	M	MP:0004101	abnormal brain interneuron morphology	Iqsec2<em1Frk>/Y	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6392615	M	MP:0004753	abnormal miniature excitatory postsynaptic currents	Iqsec2<em1Frk>/Y	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6392615	M	MP:0002566	abnormal sexual interaction	Iqsec2<em1Frk>/Y	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6392615	M	MP:0020351	decreased vocalization	Iqsec2<em1Frk>/Y	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6392615	M	MP:0000947	convulsive seizures	Iqsec2<em1Frk>/Y	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6392615	M	MP:0002887	decreased susceptibility to pharmacologically induced seizures	Iqsec2<em1Frk>/Y	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6392615	M	MP:0001363	increased anxiety-related response	Iqsec2<em1Frk>/Y	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6392615	M	MP:0003354	astrocytosis	Iqsec2<em1Frk>/Y	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6392615	M	MP:0001732	postnatal growth retardation	Iqsec2<em1Frk>/Y	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6392615	M	MP:0031391	increased locomotor activity	Iqsec2<em1Frk>/Y	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6392615	M	MP:0002083	premature death	Iqsec2<em1Frk>/Y	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6392617	F	MP:0012348	decreased susceptibility to induction of seizure by inducing agent	Iqsec2<em1Frk>/Iqsec2<+>	involves: C3HeB/FeJ * C57BL/6NJ	N	31978606
MGI:6393300	F	MP:0012307	impaired spatial learning	Iqsec2<em1Alev>/Iqsec2<em1Alev>	C57BL/6J-Iqsec2<em1Alev>	N	30842726
MGI:6393655	M	MP:0009401	increased skeletal muscle fiber diameter	Atp7a<tm1.2Mlke>/Y	involves: C57BL/6J	N	27293072
MGI:6393655	M	MP:0005621	abnormal cell physiology	Atp7a<tm1.2Mlke>/Y	involves: C57BL/6J	N	27293072
MGI:6393655	M	MP:0011214	increased brain copper level	Atp7a<tm1.2Mlke>/Y	involves: C57BL/6J	N	27293072
MGI:6393655	M	MP:0003952	abnormal copper level	Atp7a<tm1.2Mlke>/Y	involves: C57BL/6J	N	27293072
MGI:6393655	M	MP:0003631	nervous system phenotype	Atp7a<tm1.2Mlke>/Y	involves: C57BL/6J	Y	27293072
MGI:6393655	M	MP:0005386	behavior/neurological phenotype	Atp7a<tm1.2Mlke>/Y	involves: C57BL/6J	Y	27293072
MGI:6393655	M	MP:0003084	abnormal skeletal muscle fiber morphology	Atp7a<tm1.2Mlke>/Y	involves: C57BL/6J	N	27293072
MGI:6393881	F	MP:0001458	abnormal object recognition memory	Tmprss9<tm1.3Hzo>/Tmprss9<tm1.3Hzo>	involves: 129S1/Sv * C57BL/6J * C57BL/6NTac	N	31943016
MGI:6393881	F	MP:0001260	increased body weight	Tmprss9<tm1.3Hzo>/Tmprss9<tm1.3Hzo>	involves: 129S1/Sv * C57BL/6J * C57BL/6NTac	N	31943016
MGI:6393881	F	MP:0001973	increased thermal nociceptive threshold	Tmprss9<tm1.3Hzo>/Tmprss9<tm1.3Hzo>	involves: 129S1/Sv * C57BL/6J * C57BL/6NTac	N	31943016
MGI:6394025	M	MP:0010090	increased circulating creatine kinase level	Dmd<em#Tve>/Y	involves: C57BL/6 * CBA	N	31028078
MGI:6394025	M	MP:0000752	dystrophic muscle	Dmd<em#Tve>/Y	involves: C57BL/6 * CBA	N	31028078
MGI:6394025	M	MP:0000747	muscle weakness	Dmd<em#Tve>/Y	involves: C57BL/6 * CBA	N	31028078
MGI:6394025	M	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<em#Tve>/Y	involves: C57BL/6 * CBA	N	31028078
MGI:6394025	M	MP:0004121	abnormal sarcolemma morphology	Dmd<em#Tve>/Y	involves: C57BL/6 * CBA	N	31028078
MGI:6394025	M	MP:0009414	skeletal muscle fiber necrosis	Dmd<em#Tve>/Y	involves: C57BL/6 * CBA	N	31028078
MGI:6394025	M	MP:0008489	slow postnatal weight gain	Dmd<em#Tve>/Y	involves: C57BL/6 * CBA	N	31028078
MGI:6394025	M	MP:0009412	skeletal muscle fiber degeneration	Dmd<em#Tve>/Y	involves: C57BL/6 * CBA	N	31028078
MGI:6394025	M	MP:0009419	skeletal muscle fibrosis	Dmd<em#Tve>/Y	involves: C57BL/6 * CBA	N	31028078
MGI:6394025	M	MP:0001260	increased body weight	Dmd<em#Tve>/Y	involves: C57BL/6 * CBA	N	31028078
MGI:6394025	M	MP:0009402	decreased skeletal muscle fiber diameter	Dmd<em#Tve>/Y	involves: C57BL/6 * CBA	N	31028078
MGI:6394127	F	MP:0001447	abnormal nest building behavior	Shank3<tm2.1Bux>/Shank3<tm2.1Bux>	B6(Cg)-Shank3<tm2.1Bux>	N	30302388
MGI:6394127	M	MP:0002566	abnormal sexual interaction	Shank3<tm2.1Bux>/Shank3<tm2.1Bux>	B6(Cg)-Shank3<tm2.1Bux>	N	30302388
MGI:6394230	M	MP:0000194	increased circulating calcium level	Chct1<tm1b(EUCOMM)Wtsi>/Chct1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Chct1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6394232	F	MP:0013772	increased effector memory T-helper cell number	3425401B19Rik<em2(IMPC)Ccpcz>/3425401B19Rik<em2(IMPC)Ccpcz>	C57BL/6NCrl-3425401B19Rik<em2(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:6394232	M	MP:0005011	increased eosinophil cell number	3425401B19Rik<em2(IMPC)Ccpcz>/3425401B19Rik<em2(IMPC)Ccpcz>	C57BL/6NCrl-3425401B19Rik<em2(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:6394232	M	MP:0005628	decreased circulating potassium level	3425401B19Rik<em2(IMPC)Ccpcz>/3425401B19Rik<em2(IMPC)Ccpcz>	C57BL/6NCrl-3425401B19Rik<em2(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:6394233	M	MP:0002966	decreased circulating alkaline phosphatase level	4930505A04Rik<tm1b(KOMP)Wtsi>/4930505A04Rik<tm1b(KOMP)Wtsi>	C57BL/6N-4930505A04Rik<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6394233	M	MP:0005560	decreased circulating glucose level	4930505A04Rik<tm1b(KOMP)Wtsi>/4930505A04Rik<tm1b(KOMP)Wtsi>	C57BL/6N-4930505A04Rik<tm1b(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6394235	F	MP:0002092	abnormal eye morphology	Abhd13<em1(IMPC)Mbp>/Abhd13<em1(IMPC)Mbp>	C57BL/6NCrl-Abhd13<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394235	M	MP:0001415	increased exploration in new environment	Abhd13<em1(IMPC)Mbp>/Abhd13<em1(IMPC)Mbp>	C57BL/6NCrl-Abhd13<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394235	F	MP:0004953	decreased spleen weight	Abhd13<em1(IMPC)Mbp>/Abhd13<em1(IMPC)Mbp>	C57BL/6NCrl-Abhd13<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394236	F	MP:0001325	abnormal retina morphology	Abhd17b<em1(IMPC)J>/Abhd17b<em1(IMPC)J>	C57BL/6NJ-Abhd17b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394236	M	MP:0020870	decreased thigmotaxis	Abhd17b<em1(IMPC)J>/Abhd17b<em1(IMPC)J>	C57BL/6NJ-Abhd17b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394236	F	MP:0002546	mydriasis	Abhd17b<em1(IMPC)J>/Abhd17b<em1(IMPC)J>	C57BL/6NJ-Abhd17b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394238	M	MP:0001406	abnormal gait	Acy1<em1(IMPC)J>/Acy1<em1(IMPC)J>	C57BL/6NJ-Acy1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394238	F	MP:0004122	abnormal sinus arrhythmia	Acy1<em1(IMPC)J>/Acy1<em1(IMPC)J>	C57BL/6NJ-Acy1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394238	F	MP:0005344	increased circulating bilirubin level	Acy1<em1(IMPC)J>/Acy1<em1(IMPC)J>	C57BL/6NJ-Acy1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394239	F	MP:0001417	decreased exploration in new environment	Adnp2<em3(IMPC)Tcp>/Adnp2<+>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394239	F	MP:0002989	small kidney	Adnp2<em3(IMPC)Tcp>/Adnp2<+>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394239	F	MP:0005313	absent adrenal gland	Adnp2<em3(IMPC)Tcp>/Adnp2<+>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394239	F	MP:0002637	small uterus	Adnp2<em3(IMPC)Tcp>/Adnp2<+>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394239	F	MP:0000703	abnormal thymus morphology	Adnp2<em3(IMPC)Tcp>/Adnp2<+>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394239	F	MP:0000692	small spleen	Adnp2<em3(IMPC)Tcp>/Adnp2<+>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394239	F	MP:0001126	abnormal ovary morphology	Adnp2<em3(IMPC)Tcp>/Adnp2<+>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394239	M	MP:0002768	small adrenal glands	Adnp2<em3(IMPC)Tcp>/Adnp2<+>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394239	F	MP:0000157	abnormal sternum morphology	Adnp2<em3(IMPC)Tcp>/Adnp2<+>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394239	F	MP:0000702	enlarged lymph nodes	Adnp2<em3(IMPC)Tcp>/Adnp2<+>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394239	M	MP:0000598	abnormal liver morphology	Adnp2<em3(IMPC)Tcp>/Adnp2<+>	C57BL/6NCrl-Adnp2<em3(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394240	F	MP:0002968	increased circulating alkaline phosphatase level	Anapc1<em1(IMPC)J>/Anapc1<+>	C57BL/6NJ-Anapc1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394241	M	MP:0010124	decreased bone mineral content	Ankrd52<em1(IMPC)J>/Ankrd52<+>	C57BL/6NJ-Ankrd52<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394241	M	MP:0001697	abnormal embryo size	Ankrd52<em1(IMPC)J>/Ankrd52<+>	C57BL/6NJ-Ankrd52<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394241	F	MP:0000218	increased leukocyte cell number	Ankrd52<em1(IMPC)J>/Ankrd52<+>	C57BL/6NJ-Ankrd52<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394242	F	MP:0001293	anophthalmia	Ankrd52<em1(IMPC)J>/Ankrd52<em1(IMPC)J>	C57BL/6NJ-Ankrd52<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394244	M	MP:0005178	increased circulating cholesterol level	Ano8<em1(IMPC)J>/Ano8<em1(IMPC)J>	C57BL/6NJ-Ano8<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394246	M	MP:0001566	increased circulating phosphate level	Apmap<em1(IMPC)J>/Apmap<em1(IMPC)J>	C57BL/6NJ-Apmap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394246	F	MP:0010053	decreased grip strength	Apmap<em1(IMPC)J>/Apmap<em1(IMPC)J>	C57BL/6NJ-Apmap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394246	M	MP:0001556	increased circulating HDL cholesterol level	Apmap<em1(IMPC)J>/Apmap<em1(IMPC)J>	C57BL/6NJ-Apmap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394246	F	MP:0002098	abnormal vibrissa morphology	Apmap<em1(IMPC)J>/Apmap<em1(IMPC)J>	C57BL/6NJ-Apmap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394246	M	MP:0004222	iris synechia	Apmap<em1(IMPC)J>/Apmap<em1(IMPC)J>	C57BL/6NJ-Apmap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394246	M	MP:0003961	decreased lean body mass	Apmap<em1(IMPC)J>/Apmap<em1(IMPC)J>	C57BL/6NJ-Apmap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394246	M	MP:0001486	abnormal startle reflex	Apmap<em1(IMPC)J>/Apmap<em1(IMPC)J>	C57BL/6NJ-Apmap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394246	F	MP:0000452	abnormal mouth morphology	Apmap<em1(IMPC)J>/Apmap<em1(IMPC)J>	C57BL/6NJ-Apmap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394246	M	MP:0010024	increased total body fat amount	Apmap<em1(IMPC)J>/Apmap<em1(IMPC)J>	C57BL/6NJ-Apmap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394246	M	MP:0002941	increased circulating alanine transaminase level	Apmap<em1(IMPC)J>/Apmap<em1(IMPC)J>	C57BL/6NJ-Apmap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394247	M	MP:0008810	increased circulating iron level	Apoo<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Apoo<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6394248	F	MP:0003385	abnormal body wall morphology	Arhgap21<em1(IMPC)J>/Arhgap21<em1(IMPC)J>	C57BL/6NJ-Arhgap21<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394249	F	MP:0002953	thick ventricular wall	Ascc1<em1(IMPC)Bay>/Ascc1<+>	C57BL/6N-Ascc1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394249	M	MP:0011962	increased cornea thickness	Ascc1<em1(IMPC)Bay>/Ascc1<+>	C57BL/6N-Ascc1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394250	M	MP:0005179	decreased circulating cholesterol level	Atad3a<tm1a(KOMP)Wtsi>/Atad3a<+>	C57BL/6N-Atad3a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6394250	M	MP:0000186	decreased circulating HDL cholesterol level	Atad3a<tm1a(KOMP)Wtsi>/Atad3a<+>	C57BL/6N-Atad3a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6394251	F	MP:0004924	abnormal behavior	Atp1b3<em1(IMPC)Bay>/Atp1b3<+>	C57BL/6N-Atp1b3<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394251	F	MP:0020870	decreased thigmotaxis	Atp1b3<em1(IMPC)Bay>/Atp1b3<+>	C57BL/6N-Atp1b3<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394251	F	MP:0001399	hyperactivity	Atp1b3<em1(IMPC)Bay>/Atp1b3<+>	C57BL/6N-Atp1b3<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394252	M	MP:0002075	abnormal coat/hair pigmentation	Atp2b3<em1(IMPC)J>/Y	C57BL/6NJ-Atp2b3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394253	F	MP:0005333	decreased heart rate	Atp2b3<em1(IMPC)J>/Atp2b3<em1(IMPC)J>	C57BL/6NJ-Atp2b3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394253	F	MP:0020870	decreased thigmotaxis	Atp2b3<em1(IMPC)J>/Atp2b3<em1(IMPC)J>	C57BL/6NJ-Atp2b3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394253	F	MP:0001402	decreased locomotor activity	Atp2b3<em1(IMPC)J>/Atp2b3<em1(IMPC)J>	C57BL/6NJ-Atp2b3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394253	F	MP:0001399	hyperactivity	Atp2b3<em1(IMPC)J>/Atp2b3<em1(IMPC)J>	C57BL/6NJ-Atp2b3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394253	F	MP:0002075	abnormal coat/hair pigmentation	Atp2b3<em1(IMPC)J>/Atp2b3<em1(IMPC)J>	C57BL/6NJ-Atp2b3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394255	F	MP:0003733	abnormal retina inner nuclear layer morphology	Bcl7b<tm1b(EUCOMM)Wtsi>/Bcl7b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bcl7b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6394255	F	MP:0010052	increased grip strength	Bcl7b<tm1b(EUCOMM)Wtsi>/Bcl7b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bcl7b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6394255	M	MP:0011110	preweaning lethality, incomplete penetrance	Bcl7b<tm1b(EUCOMM)Wtsi>/Bcl7b<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bcl7b<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6394256	F	MP:0000220	increased monocyte cell number	Bdkrb1<em1(IMPC)H>/Bdkrb1<em1(IMPC)H>	B6N;B6NTac-Bdkrb1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394256	F	MP:0010052	increased grip strength	Bdkrb1<em1(IMPC)H>/Bdkrb1<em1(IMPC)H>	B6N;B6NTac-Bdkrb1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394256	F	MP:0002968	increased circulating alkaline phosphatase level	Bdkrb1<em1(IMPC)H>/Bdkrb1<em1(IMPC)H>	B6N;B6NTac-Bdkrb1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394256	F	MP:0000222	decreased neutrophil cell number	Bdkrb1<em1(IMPC)H>/Bdkrb1<em1(IMPC)H>	B6N;B6NTac-Bdkrb1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394256	F	MP:0012362	increased large unstained cell number	Bdkrb1<em1(IMPC)H>/Bdkrb1<em1(IMPC)H>	B6N;B6NTac-Bdkrb1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394257	M	MP:0000642	enlarged adrenal glands	Bmerb1<em1(IMPC)Ccpcz>/Bmerb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Bmerb1<em1(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:6394257	M	MP:0000613	abnormal salivary gland morphology	Bmerb1<em1(IMPC)Ccpcz>/Bmerb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Bmerb1<em1(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:6394257	M	MP:0000639	abnormal adrenal gland morphology	Bmerb1<em1(IMPC)Ccpcz>/Bmerb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Bmerb1<em1(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:6394257	M	MP:0000538	abnormal urinary bladder morphology	Bmerb1<em1(IMPC)Ccpcz>/Bmerb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Bmerb1<em1(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:6394258	M	MP:0000702	enlarged lymph nodes	Brap<em1(IMPC)Mbp>/Brap<+>	C57BL/6NCrl-Brap<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394258	M	MP:0020421	increased freezing behavior	Brap<em1(IMPC)Mbp>/Brap<+>	C57BL/6NCrl-Brap<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394258	M	MP:0002339	abnormal lymph node morphology	Brap<em1(IMPC)Mbp>/Brap<+>	C57BL/6NCrl-Brap<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394260	M	MP:0005553	increased circulating creatinine level	Capza2<tm1b(KOMP)Wtsi>/Capza2<+>	C57BL/6N-Capza2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6394262	M	MP:0001417	decreased exploration in new environment	Cct5<em1(IMPC)Tcp>/Cct5<+>	C57BL/6NCrl-Cct5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394262	F	MP:0002060	abnormal skin morphology	Cct5<em1(IMPC)Tcp>/Cct5<+>	C57BL/6NCrl-Cct5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394262	F	MP:0001120	abnormal uterus morphology	Cct5<em1(IMPC)Tcp>/Cct5<+>	C57BL/6NCrl-Cct5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394262	M	MP:0001325	abnormal retina morphology	Cct5<em1(IMPC)Tcp>/Cct5<+>	C57BL/6NCrl-Cct5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394265	F	MP:0001399	hyperactivity	Cdk17<em1(IMPC)J>/Cdk17<+>	C57BL/6NJ-Cdk17<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394266	M	MP:0000443	abnormal snout morphology	Cdk17<em1(IMPC)J>/Cdk17<em1(IMPC)J>	C57BL/6NJ-Cdk17<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394266	F	MP:0001697	abnormal embryo size	Cdk17<em1(IMPC)J>/Cdk17<em1(IMPC)J>	C57BL/6NJ-Cdk17<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394266	M	MP:0002574	increased vertical activity	Cdk17<em1(IMPC)J>/Cdk17<em1(IMPC)J>	C57BL/6NJ-Cdk17<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394267	F	MP:0005553	increased circulating creatinine level	Cdk18<em1(IMPC)J>/Cdk18<em1(IMPC)J>	C57BL/6NJ-Cdk18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394268	M	MP:0010123	increased bone mineral content	Ceacam11<em1(IMPC)Wtsi>/Ceacam11<em1(IMPC)Wtsi>	C57BL/6N-Ceacam11<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:6394269	F	MP:0002989	small kidney	Cep55<em1(IMPC)Tcp>/Cep55<+>	C57BL/6NCrl-Cep55<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394269	M	MP:0000157	abnormal sternum morphology	Cep55<em1(IMPC)Tcp>/Cep55<+>	C57BL/6NCrl-Cep55<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394269	F	MP:0001126	abnormal ovary morphology	Cep55<em1(IMPC)Tcp>/Cep55<+>	C57BL/6NCrl-Cep55<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394269	F	MP:0002637	small uterus	Cep55<em1(IMPC)Tcp>/Cep55<+>	C57BL/6NCrl-Cep55<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394270	M	MP:0002075	abnormal coat/hair pigmentation	Cgref1<em1(IMPC)J>/Cgref1<em1(IMPC)J>	C57BL/6NJ-Cgref1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394270	M	MP:0002833	increased heart weight	Cgref1<em1(IMPC)J>/Cgref1<em1(IMPC)J>	C57BL/6NJ-Cgref1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394270	M	MP:0000218	increased leukocyte cell number	Cgref1<em1(IMPC)J>/Cgref1<em1(IMPC)J>	C57BL/6NJ-Cgref1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394270	F	MP:0002966	decreased circulating alkaline phosphatase level	Cgref1<em1(IMPC)J>/Cgref1<em1(IMPC)J>	C57BL/6NJ-Cgref1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394277	M	MP:0000274	enlarged heart	Daxx<em1(IMPC)Mbp>/Daxx<+>	C57BL/6N-Daxx<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394278	M	MP:0005564	increased hemoglobin content	Dhps<tm2a(EUCOMM)Wtsi>/Dhps<+>	C57BL/6N-Dhps<tm2a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6394281	M	MP:0002075	abnormal coat/hair pigmentation	Dnase1l2<em1(IMPC)J>/Dnase1l2<em1(IMPC)J>	C57BL/6NJ-Dnase1l2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394281	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Dnase1l2<em1(IMPC)J>/Dnase1l2<em1(IMPC)J>	C57BL/6NJ-Dnase1l2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394281	F	MP:0001399	hyperactivity	Dnase1l2<em1(IMPC)J>/Dnase1l2<em1(IMPC)J>	C57BL/6NJ-Dnase1l2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394281	M	MP:0001486	abnormal startle reflex	Dnase1l2<em1(IMPC)J>/Dnase1l2<em1(IMPC)J>	C57BL/6NJ-Dnase1l2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394281	F	MP:0005566	decreased blood urea nitrogen level	Dnase1l2<em1(IMPC)J>/Dnase1l2<em1(IMPC)J>	C57BL/6NJ-Dnase1l2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394282	F	MP:0001404	no spontaneous movement	E2f3<tm1b(KOMP)Wtsi>/E2f3<tm1b(KOMP)Wtsi>	C57BL/6N-E2f3<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6394282	F	MP:0001697	abnormal embryo size	E2f3<tm1b(KOMP)Wtsi>/E2f3<tm1b(KOMP)Wtsi>	C57BL/6N-E2f3<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6394284	F	MP:0005632	decreased circulating aspartate transaminase level	Emg1<tm1.1(KOMP)Wtsi>/Emg1<+>	C57BL/6N-Emg1<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6394284	F	MP:0003733	abnormal retina inner nuclear layer morphology	Emg1<tm1.1(KOMP)Wtsi>/Emg1<+>	C57BL/6N-Emg1<tm1.1(KOMP)Wtsi>/Bay	N	MGI:5576271
MGI:6394286	F	MP:0003896	prolonged PR interval	Eral1<em1(IMPC)Bay>/Eral1<+>	C57BL/6N-Eral1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394287	M	MP:0013279	increased fasting circulating glucose level	Ercc5<tm2b(EUCOMM)Hmgu>/Ercc5<+>	C57BL/6N-Ercc5<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6394288	M	MP:0001415	increased exploration in new environment	Exoc1<em1(IMPC)Mbp>/Exoc1<+>	C57BL/6N-Exoc1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394290	F	MP:0000709	enlarged thymus	Arb2a<em2(IMPC)Ccpcz>/Arb2a<em2(IMPC)Ccpcz>	C57BL/6NCrl-Arb2a<em2(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:6394290	F	MP:0000703	abnormal thymus morphology	Arb2a<em2(IMPC)Ccpcz>/Arb2a<em2(IMPC)Ccpcz>	C57BL/6NCrl-Arb2a<em2(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:6394290	F	MP:0013678	decreased Ly6C-positive NK T cell number	Arb2a<em2(IMPC)Ccpcz>/Arb2a<em2(IMPC)Ccpcz>	C57BL/6NCrl-Arb2a<em2(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:6394290	F	MP:0000598	abnormal liver morphology	Arb2a<em2(IMPC)Ccpcz>/Arb2a<em2(IMPC)Ccpcz>	C57BL/6NCrl-Arb2a<em2(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:6394290	M	MP:0003402	decreased liver weight	Arb2a<em2(IMPC)Ccpcz>/Arb2a<em2(IMPC)Ccpcz>	C57BL/6NCrl-Arb2a<em2(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:6394290	F	MP:0005343	increased circulating aspartate transaminase level	Arb2a<em2(IMPC)Ccpcz>/Arb2a<em2(IMPC)Ccpcz>	C57BL/6NCrl-Arb2a<em2(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:6394293	M	MP:0000572	abnormal autopod morphology	Frmpd1<em1(IMPC)J>/Frmpd1<em1(IMPC)J>	C57BL/6NJ-Frmpd1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394293	F	MP:0010053	decreased grip strength	Frmpd1<em1(IMPC)J>/Frmpd1<em1(IMPC)J>	C57BL/6NJ-Frmpd1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394293	M	MP:0000556	abnormal hindlimb morphology	Frmpd1<em1(IMPC)J>/Frmpd1<em1(IMPC)J>	C57BL/6NJ-Frmpd1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394295	F	MP:0005553	increased circulating creatinine level	Gckr<em1(IMPC)H>/Gckr<em1(IMPC)H>	C57BL/6NTac-Gckr<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394295	F	MP:0005565	increased blood urea nitrogen level	Gckr<em1(IMPC)H>/Gckr<em1(IMPC)H>	C57BL/6NTac-Gckr<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394296	M	MP:0002599	increased mean platelet volume	Gemin5<em1(IMPC)H>/Gemin5<+>	C57BL/6N-Gemin5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394298	M	MP:0001556	increased circulating HDL cholesterol level	Ceacam23<em1(IMPC)Wtsi>/Ceacam23<em1(IMPC)Wtsi>	C57BL/6N-Ceacam23<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:6394299	F	MP:0011965	decreased total retina thickness	Gnb1<em1(IMPC)Bay>/Gnb1<+>	C57BL/6N-Gnb1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394299	F	MP:0002574	increased vertical activity	Gnb1<em1(IMPC)Bay>/Gnb1<+>	C57BL/6N-Gnb1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394299	F	MP:0003731	abnormal retina outer nuclear layer morphology	Gnb1<em1(IMPC)Bay>/Gnb1<+>	C57BL/6N-Gnb1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394300	M	MP:0002874	decreased hemoglobin content	Gpr142<tm1.1(KOMP)Vlcg>/Gpr142<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpr142<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6394300	M	MP:0002833	increased heart weight	Gpr142<tm1.1(KOMP)Vlcg>/Gpr142<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpr142<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6394301	M	MP:0011951	increased cardiac stroke volume	Grem2<em1(IMPC)Bay>/Grem2<+>	C57BL/6N-Grem2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394303	M	MP:0000274	enlarged heart	Grp<em1(IMPC)H>/Grp<em1(IMPC)H>	C57BL/6NTac-Grp<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394303	F	MP:0004924	abnormal behavior	Grp<em1(IMPC)H>/Grp<em1(IMPC)H>	C57BL/6NTac-Grp<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394303	F	MP:0020870	decreased thigmotaxis	Grp<em1(IMPC)H>/Grp<em1(IMPC)H>	C57BL/6NTac-Grp<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394304	M	MP:0002075	abnormal coat/hair pigmentation	Hnrnph2<em1(IMPC)J>/Y	C57BL/6NJ-Hnrnph2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394304	M	MP:0000367	abnormal coat/ hair morphology	Hnrnph2<em1(IMPC)J>/Y	C57BL/6NJ-Hnrnph2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394304	M	MP:0001284	absent vibrissae	Hnrnph2<em1(IMPC)J>/Y	C57BL/6NJ-Hnrnph2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394304	M	MP:0001529	abnormal vocalization	Hnrnph2<em1(IMPC)J>/Y	C57BL/6NJ-Hnrnph2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394307	M	MP:0001925	male infertility	Idh3b<em1(IMPC)J>/Idh3b<em1(IMPC)J>	C57BL/6NJ-Idh3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394307	F	MP:0001513	limb grasping	Idh3b<em1(IMPC)J>/Idh3b<em1(IMPC)J>	C57BL/6NJ-Idh3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394307	F	MP:0001523	impaired righting response	Idh3b<em1(IMPC)J>/Idh3b<em1(IMPC)J>	C57BL/6NJ-Idh3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394307	F	MP:0001325	abnormal retina morphology	Idh3b<em1(IMPC)J>/Idh3b<em1(IMPC)J>	C57BL/6NJ-Idh3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394307	M	MP:0001399	hyperactivity	Idh3b<em1(IMPC)J>/Idh3b<em1(IMPC)J>	C57BL/6NJ-Idh3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394307	M	MP:0002574	increased vertical activity	Idh3b<em1(IMPC)J>/Idh3b<em1(IMPC)J>	C57BL/6NJ-Idh3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394311	F	MP:0011886	increased circulating lipase level	Il4i1<tm1b(EUCOMM)Wtsi>/Il4i1<+>	C57BL/6N-Il4i1<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6394312	F	MP:0002060	abnormal skin morphology	Ing4<em1(IMPC)Tcp>/Ing4<em1(IMPC)Tcp>	C57BL/6NCrl-Ing4<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394312	F	MP:0002764	short tibia	Ing4<em1(IMPC)Tcp>/Ing4<em1(IMPC)Tcp>	C57BL/6NCrl-Ing4<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394312	M	MP:0005633	increased circulating sodium level	Ing4<em1(IMPC)Tcp>/Ing4<em1(IMPC)Tcp>	C57BL/6NCrl-Ing4<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394312	M	MP:0002966	decreased circulating alkaline phosphatase level	Ing4<em1(IMPC)Tcp>/Ing4<em1(IMPC)Tcp>	C57BL/6NCrl-Ing4<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394312	F	MP:0002989	small kidney	Ing4<em1(IMPC)Tcp>/Ing4<em1(IMPC)Tcp>	C57BL/6NCrl-Ing4<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394312	M	MP:0003019	increased circulating chloride level	Ing4<em1(IMPC)Tcp>/Ing4<em1(IMPC)Tcp>	C57BL/6NCrl-Ing4<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394312	M	MP:0005016	decreased lymphocyte cell number	Ing4<em1(IMPC)Tcp>/Ing4<em1(IMPC)Tcp>	C57BL/6NCrl-Ing4<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394312	M	MP:0000219	increased neutrophil cell number	Ing4<em1(IMPC)Tcp>/Ing4<em1(IMPC)Tcp>	C57BL/6NCrl-Ing4<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394312	M	MP:0005419	decreased circulating serum albumin level	Ing4<em1(IMPC)Tcp>/Ing4<em1(IMPC)Tcp>	C57BL/6NCrl-Ing4<em2(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394316	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Itgb3bp<em1(IMPC)J>/Itgb3bp<em1(IMPC)J>	C57BL/6NJ-Itgb3bp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394318	M	MP:0005293	impaired glucose tolerance	Knl1<tm1b(EUCOMM)Hmgu>/Knl1<+>	C57BL/6N-Knl1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6394319	F	MP:0010053	decreased grip strength	Krt25<em1(IMPC)J>/Krt25<em1(IMPC)J>	C57BL/6NJ-Krt25<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394320	M	MP:0005633	increased circulating sodium level	Krt77<em1(IMPC)J>/Krt77<em1(IMPC)J>	C57BL/6NJ-Krt77<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394321	M	MP:0011100	preweaning lethality, complete penetrance	Lemd2<em1(IMPC)Bay>/Lemd2<em1(IMPC)Bay>	C57BL/6N-Lemd2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394326	M	MP:0005016	decreased lymphocyte cell number	Mgrn1<em1(IMPC)Tcp>/Mgrn1<+>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394326	F	MP:0001120	abnormal uterus morphology	Mgrn1<em1(IMPC)Tcp>/Mgrn1<+>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394326	M	MP:0004952	increased spleen weight	Mgrn1<em1(IMPC)Tcp>/Mgrn1<+>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394326	M	MP:0010025	decreased total body fat amount	Mgrn1<em1(IMPC)Tcp>/Mgrn1<+>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394326	F	MP:0005013	increased lymphocyte cell number	Mgrn1<em1(IMPC)Tcp>/Mgrn1<+>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394326	M	MP:0011874	enlarged urinary bladder	Mgrn1<em1(IMPC)Tcp>/Mgrn1<+>	C57BL/6NCrl-Mgrn1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394330	M	MP:0002135	abnormal kidney morphology	Mrpl12<em1(IMPC)Tcp>/Mrpl12<+>	C57BL/6NCrl-Mrpl12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394330	M	MP:0000702	enlarged lymph nodes	Mrpl12<em1(IMPC)Tcp>/Mrpl12<+>	C57BL/6NCrl-Mrpl12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394332	F	MP:0010053	decreased grip strength	Myom2<em1(IMPC)J>/Myom2<em1(IMPC)J>	C57BL/6NJ-Myom2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394332	F	MP:0002075	abnormal coat/hair pigmentation	Myom2<em1(IMPC)J>/Myom2<em1(IMPC)J>	C57BL/6NJ-Myom2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394333	F	MP:0001399	hyperactivity	Naa25<em1(IMPC)Tcp>/Naa25<+>	C57BL/6NCrl-Naa25<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394333	F	MP:0000157	abnormal sternum morphology	Naa25<em1(IMPC)Tcp>/Naa25<+>	C57BL/6NCrl-Naa25<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394333	M	MP:0000702	enlarged lymph nodes	Naa25<em1(IMPC)Tcp>/Naa25<+>	C57BL/6NCrl-Naa25<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394333	F	MP:0001120	abnormal uterus morphology	Naa25<em1(IMPC)Tcp>/Naa25<+>	C57BL/6NCrl-Naa25<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394333	M	MP:0000709	enlarged thymus	Naa25<em1(IMPC)Tcp>/Naa25<+>	C57BL/6NCrl-Naa25<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394334	F	MP:0000689	abnormal spleen morphology	Naa50<em1(IMPC)Mbp>/Naa50<+>	C57BL/6N-Naa50<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394334	F	MP:0000691	enlarged spleen	Naa50<em1(IMPC)Mbp>/Naa50<+>	C57BL/6N-Naa50<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394335	F	MP:0002092	abnormal eye morphology	Ndrg3<em1(IMPC)Mbp>/Ndrg3<+>	C57BL/6NCrl-Ndrg3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394335	M	MP:0001147	small testis	Ndrg3<em1(IMPC)Mbp>/Ndrg3<+>	C57BL/6NCrl-Ndrg3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394335	F	MP:0003068	enlarged kidney	Ndrg3<em1(IMPC)Mbp>/Ndrg3<+>	C57BL/6NCrl-Ndrg3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394335	F	MP:0000691	enlarged spleen	Ndrg3<em1(IMPC)Mbp>/Ndrg3<+>	C57BL/6NCrl-Ndrg3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394335	M	MP:0020421	increased freezing behavior	Ndrg3<em1(IMPC)Mbp>/Ndrg3<+>	C57BL/6NCrl-Ndrg3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394335	M	MP:0001146	abnormal testis morphology	Ndrg3<em1(IMPC)Mbp>/Ndrg3<+>	C57BL/6NCrl-Ndrg3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394335	M	MP:0000195	decreased circulating calcium level	Ndrg3<em1(IMPC)Mbp>/Ndrg3<+>	C57BL/6NCrl-Ndrg3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394336	F	MP:0002953	thick ventricular wall	Ndufa6<em1(IMPC)Bay>/Ndufa6<+>	C57BL/6N-Ndufa6<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394336	F	MP:0005333	decreased heart rate	Ndufa6<em1(IMPC)Bay>/Ndufa6<+>	C57BL/6N-Ndufa6<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394336	F	MP:0010506	prolonged RR interval	Ndufa6<em1(IMPC)Bay>/Ndufa6<+>	C57BL/6N-Ndufa6<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394337	F	MP:0000157	abnormal sternum morphology	Nelfa<em1(IMPC)Tcp>/Nelfa<+>	C57BL/6NCrl-Nelfa<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394337	M	MP:0002833	increased heart weight	Nelfa<em1(IMPC)Tcp>/Nelfa<+>	C57BL/6NCrl-Nelfa<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394337	M	MP:0008528	polycystic kidney	Nelfa<em1(IMPC)Tcp>/Nelfa<+>	C57BL/6NCrl-Nelfa<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394337	M	MP:0011874	enlarged urinary bladder	Nelfa<em1(IMPC)Tcp>/Nelfa<+>	C57BL/6NCrl-Nelfa<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394337	M	MP:0010067	increased red blood cell distribution width	Nelfa<em1(IMPC)Tcp>/Nelfa<+>	C57BL/6NCrl-Nelfa<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394337	M	MP:0004952	increased spleen weight	Nelfa<em1(IMPC)Tcp>/Nelfa<+>	C57BL/6NCrl-Nelfa<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394340	F	MP:0000691	enlarged spleen	Nsa2<em1(IMPC)Mbp>/Nsa2<+>	C57BL/6N-Nsa2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394340	F	MP:0000689	abnormal spleen morphology	Nsa2<em1(IMPC)Mbp>/Nsa2<+>	C57BL/6N-Nsa2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394341	F	MP:0009455	enhanced cued conditioning behavior	Nufip1<em1(IMPC)Mbp>/Nufip1<+>	C57BL/6NCrl-Nufip1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394341	F	MP:0020421	increased freezing behavior	Nufip1<em1(IMPC)Mbp>/Nufip1<+>	C57BL/6NCrl-Nufip1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394345	F	MP:0002092	abnormal eye morphology	Opn3<em1(IMPC)Mbp>/Opn3<em1(IMPC)Mbp>	C57BL/6NCrl-Opn3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394345	M	MP:0002606	increased basophil cell number	Opn3<em1(IMPC)Mbp>/Opn3<em1(IMPC)Mbp>	C57BL/6NCrl-Opn3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394346	M	MP:0010025	decreased total body fat amount	Orc1<tm1a(KOMP)Wtsi>/Orc1<+>	C57BL/6N-Orc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6394346	M	MP:0003960	increased lean body mass	Orc1<tm1a(KOMP)Wtsi>/Orc1<+>	C57BL/6N-Orc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6394346	M	MP:0000062	increased bone mineral density	Orc1<tm1a(KOMP)Wtsi>/Orc1<+>	C57BL/6N-Orc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6394346	M	MP:0010123	increased bone mineral content	Orc1<tm1a(KOMP)Wtsi>/Orc1<+>	C57BL/6N-Orc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6394346	F	MP:0010052	increased grip strength	Orc1<tm1a(KOMP)Wtsi>/Orc1<+>	C57BL/6N-Orc1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6394348	M	MP:0001417	decreased exploration in new environment	Pah<em1(IMPC)Tcp>/Pah<+>	C57BL/6NCrl-Pah<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394348	F	MP:0000692	small spleen	Pah<em1(IMPC)Tcp>/Pah<+>	C57BL/6NCrl-Pah<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394348	M	MP:0000157	abnormal sternum morphology	Pah<em1(IMPC)Tcp>/Pah<+>	C57BL/6NCrl-Pah<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394350	F	MP:0005343	increased circulating aspartate transaminase level	Patj<em1(IMPC)J>/Patj<em1(IMPC)J>	C57BL/6NJ-Patj<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394351	M	MP:0001392	abnormal locomotor behavior	Pcdhgb1<em1(IMPC)J>/Pcdhgb1<em1(IMPC)J>	C57BL/6NJ-Pcdhgb1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394352	M	MP:0002631	abnormal epididymis morphology	Pcnp<em1(IMPC)Mbp>/Pcnp<+>	C57BL/6N-Pcnp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394352	M	MP:0002060	abnormal skin morphology	Pcnp<em1(IMPC)Mbp>/Pcnp<+>	C57BL/6N-Pcnp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394352	M	MP:0004931	enlarged epididymis	Pcnp<em1(IMPC)Mbp>/Pcnp<+>	C57BL/6N-Pcnp<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394353	M	MP:0010097	abnormal retina blood vessel morphology	Pdhb<em1(IMPC)Bay>/Pdhb<+>	C57BL/6N-Pdhb<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394356	M	MP:0005343	increased circulating aspartate transaminase level	Phip<em1(IMPC)Tcp>/Phip<+>	C57BL/6NCrl-Phip<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394356	M	MP:0001891	hydrocephaly	Phip<em1(IMPC)Tcp>/Phip<+>	C57BL/6NCrl-Phip<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394356	M	MP:0011874	enlarged urinary bladder	Phip<em1(IMPC)Tcp>/Phip<+>	C57BL/6NCrl-Phip<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394356	F	MP:0002637	small uterus	Phip<em1(IMPC)Tcp>/Phip<+>	C57BL/6NCrl-Phip<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394357	F	MP:0001488	increased startle reflex	Phldb2<em1(IMPC)H>/Phldb2<em1(IMPC)H>	C57BL/6NTac-Phldb2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394357	F	MP:0002606	increased basophil cell number	Phldb2<em1(IMPC)H>/Phldb2<em1(IMPC)H>	C57BL/6NTac-Phldb2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394357	F	MP:0001333	absent optic nerve	Phldb2<em1(IMPC)H>/Phldb2<em1(IMPC)H>	C57BL/6NTac-Phldb2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394359	M	MP:0002098	abnormal vibrissa morphology	Pigl<tm1b(KOMP)Wtsi>/Pigl<+>	C57BL/6N-Pigl<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6394360	F	MP:0003717	pallor	Pkmyt1<em1(IMPC)J>/Pkmyt1<em1(IMPC)J>	C57BL/6NJ-Pkmyt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394360	F	MP:0000783	abnormal forebrain morphology	Pkmyt1<em1(IMPC)J>/Pkmyt1<em1(IMPC)J>	C57BL/6NJ-Pkmyt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394360	F	MP:0000603	pale liver	Pkmyt1<em1(IMPC)J>/Pkmyt1<em1(IMPC)J>	C57BL/6NJ-Pkmyt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394360	F	MP:0003720	abnormal neural tube closure	Pkmyt1<em1(IMPC)J>/Pkmyt1<em1(IMPC)J>	C57BL/6NJ-Pkmyt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394361	F	MP:0009142	decreased prepulse inhibition	Plaur<em1(IMPC)H>/Plaur<em1(IMPC)H>	C57BL/6NTac-Plaur<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394363	M	MP:0011965	decreased total retina thickness	Pom121<tm1b(EUCOMM)Wtsi>/Pom121<+>	C57BL/6N-Pom121<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6394363	M	MP:0001510	abnormal coat appearance	Pom121<tm1b(EUCOMM)Wtsi>/Pom121<+>	C57BL/6N-Pom121<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6394368	F	MP:0000062	increased bone mineral density	Pttg1ip<em1(IMPC)H>/Pttg1ip<em1(IMPC)H>	C57BL/6NTac-Pttg1ip<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394368	F	MP:0010123	increased bone mineral content	Pttg1ip<em1(IMPC)H>/Pttg1ip<em1(IMPC)H>	C57BL/6NTac-Pttg1ip<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394368	M	MP:0005565	increased blood urea nitrogen level	Pttg1ip<em1(IMPC)H>/Pttg1ip<em1(IMPC)H>	C57BL/6NTac-Pttg1ip<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394370	F	MP:0002874	decreased hemoglobin content	Rhbdl2<tm1b(KOMP)Wtsi>/Rhbdl2<tm1b(KOMP)Wtsi>	C57BL/6N-Rhbdl2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6394370	F	MP:0002875	decreased erythrocyte cell number	Rhbdl2<tm1b(KOMP)Wtsi>/Rhbdl2<tm1b(KOMP)Wtsi>	C57BL/6N-Rhbdl2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6394370	F	MP:0000208	decreased hematocrit	Rhbdl2<tm1b(KOMP)Wtsi>/Rhbdl2<tm1b(KOMP)Wtsi>	C57BL/6N-Rhbdl2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6394370	F	MP:0001759	increased urine glucose level	Rhbdl2<tm1b(KOMP)Wtsi>/Rhbdl2<tm1b(KOMP)Wtsi>	C57BL/6N-Rhbdl2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6394374	M	MP:0003642	absent seminal vesicle	Rpe<em1(IMPC)Mbp>/Rpe<+>	C57BL/6NCrl-Rpe<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394374	M	MP:0001147	small testis	Rpe<em1(IMPC)Mbp>/Rpe<+>	C57BL/6NCrl-Rpe<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394374	M	MP:0002059	abnormal seminal vesicle morphology	Rpe<em1(IMPC)Mbp>/Rpe<+>	C57BL/6NCrl-Rpe<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394374	M	MP:0003068	enlarged kidney	Rpe<em1(IMPC)Mbp>/Rpe<+>	C57BL/6NCrl-Rpe<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394374	F	MP:0004906	enlarged uterus	Rpe<em1(IMPC)Mbp>/Rpe<+>	C57BL/6NCrl-Rpe<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394374	F	MP:0002188	small heart	Rpe<em1(IMPC)Mbp>/Rpe<+>	C57BL/6NCrl-Rpe<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394374	F	MP:0020421	increased freezing behavior	Rpe<em1(IMPC)Mbp>/Rpe<+>	C57BL/6NCrl-Rpe<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394374	M	MP:0002135	abnormal kidney morphology	Rpe<em1(IMPC)Mbp>/Rpe<+>	C57BL/6NCrl-Rpe<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394374	M	MP:0001146	abnormal testis morphology	Rpe<em1(IMPC)Mbp>/Rpe<+>	C57BL/6NCrl-Rpe<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394374	M	MP:0002997	enlarged seminal vesicle	Rpe<em1(IMPC)Mbp>/Rpe<+>	C57BL/6NCrl-Rpe<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394375	F	MP:0001399	hyperactivity	Rtl10<em1(IMPC)J>/Rtl10<em1(IMPC)J>	C57BL/6NJ-Rtl10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394375	M	MP:0002075	abnormal coat/hair pigmentation	Rtl10<em1(IMPC)J>/Rtl10<em1(IMPC)J>	C57BL/6NJ-Rtl10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394376	M	MP:0010025	decreased total body fat amount	Safb2<em1(IMPC)J>/Safb2<em1(IMPC)J>	C57BL/6NJ-Safb2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394376	F	MP:0002574	increased vertical activity	Safb2<em1(IMPC)J>/Safb2<em1(IMPC)J>	C57BL/6NJ-Safb2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394377	F	MP:0005568	increased circulating total protein level	Scamp2<em1(IMPC)J>/Scamp2<em1(IMPC)J>	C57BL/6NJ-Scamp2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394377	M	MP:0001486	abnormal startle reflex	Scamp2<em1(IMPC)J>/Scamp2<em1(IMPC)J>	C57BL/6NJ-Scamp2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394377	M	MP:0001489	decreased startle reflex	Scamp2<em1(IMPC)J>/Scamp2<em1(IMPC)J>	C57BL/6NJ-Scamp2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394377	F	MP:0012121	sclerocornea	Scamp2<em1(IMPC)J>/Scamp2<em1(IMPC)J>	C57BL/6NJ-Scamp2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394378	M	MP:0010393	shortened QRS complex duration	Sccpdh<em1(IMPC)J>/Sccpdh<em1(IMPC)J>	C57BL/6NJ-Sccpdh<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394378	M	MP:0001925	male infertility	Sccpdh<em1(IMPC)J>/Sccpdh<em1(IMPC)J>	C57BL/6NJ-Sccpdh<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394378	M	MP:0001529	abnormal vocalization	Sccpdh<em1(IMPC)J>/Sccpdh<em1(IMPC)J>	C57BL/6NJ-Sccpdh<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394379	M	MP:0001552	increased circulating triglyceride level	Sclt1<em1(IMPC)Tcp>/Sclt1<+>	C57BL/6NCrl-Sclt1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394379	M	MP:0002092	abnormal eye morphology	Sclt1<em1(IMPC)Tcp>/Sclt1<+>	C57BL/6NCrl-Sclt1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394380	F	MP:0010052	increased grip strength	Sec14l1<em1(IMPC)J>/Sec14l1<em1(IMPC)J>	C57BL/6NJ-Sec14l1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394380	F	MP:0013279	increased fasting circulating glucose level	Sec14l1<em1(IMPC)J>/Sec14l1<em1(IMPC)J>	C57BL/6NJ-Sec14l1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394380	F	MP:0001399	hyperactivity	Sec14l1<em1(IMPC)J>/Sec14l1<em1(IMPC)J>	C57BL/6NJ-Sec14l1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394382	M	MP:0005343	increased circulating aspartate transaminase level	Sfr1<em1(IMPC)Mbp>/Sfr1<+>	C57BL/6NCrl-Sfr1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394383	F	MP:0003896	prolonged PR interval	Shmt2<em1(IMPC)Bay>/Shmt2<+>	C57BL/6N-Shmt2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394383	F	MP:0004952	increased spleen weight	Shmt2<em1(IMPC)Bay>/Shmt2<+>	C57BL/6N-Shmt2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394385	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Spink12<em1(IMPC)J>/Spink12<em1(IMPC)J>	C57BL/6NJ-Spink12<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394385	M	MP:0005344	increased circulating bilirubin level	Spink12<em1(IMPC)J>/Spink12<em1(IMPC)J>	C57BL/6NJ-Spink12<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394385	M	MP:0001325	abnormal retina morphology	Spink12<em1(IMPC)J>/Spink12<em1(IMPC)J>	C57BL/6NJ-Spink12<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394385	F	MP:0002968	increased circulating alkaline phosphatase level	Spink12<em1(IMPC)J>/Spink12<em1(IMPC)J>	C57BL/6NJ-Spink12<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394385	F	MP:0001486	abnormal startle reflex	Spink12<em1(IMPC)J>/Spink12<em1(IMPC)J>	C57BL/6NJ-Spink12<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394385	M	MP:0002075	abnormal coat/hair pigmentation	Spink12<em1(IMPC)J>/Spink12<em1(IMPC)J>	C57BL/6NJ-Spink12<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394385	M	MP:0005566	decreased blood urea nitrogen level	Spink12<em1(IMPC)J>/Spink12<em1(IMPC)J>	C57BL/6NJ-Spink12<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394385	M	MP:0002941	increased circulating alanine transaminase level	Spink12<em1(IMPC)J>/Spink12<em1(IMPC)J>	C57BL/6NJ-Spink12<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394387	M	MP:0000198	decreased circulating phosphate level	Srek1<em1(IMPC)J>/Srek1<+>	C57BL/6NJ-Srek1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394390	F	MP:0002574	increased vertical activity	Srsf9<em1(IMPC)J>/Srsf9<em1(IMPC)J>	C57BL/6NJ-Srsf9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394391	M	MP:0003179	thrombocytopenia	Stk33<em1(IMPC)J>/Stk33<em1(IMPC)J>	C57BL/6NJ-Stk33<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394391	F	MP:0013279	increased fasting circulating glucose level	Stk33<em1(IMPC)J>/Stk33<em1(IMPC)J>	C57BL/6NJ-Stk33<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394391	M	MP:0001925	male infertility	Stk33<em1(IMPC)J>/Stk33<em1(IMPC)J>	C57BL/6NJ-Stk33<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394396	M	MP:0002075	abnormal coat/hair pigmentation	Tm9sf3<em1(IMPC)Mbp>/Tm9sf3<+>	C57BL/6NCrl-Tm9sf3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394396	M	MP:0001552	increased circulating triglyceride level	Tm9sf3<em1(IMPC)Mbp>/Tm9sf3<+>	C57BL/6NCrl-Tm9sf3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6394397	F	MP:0001399	hyperactivity	Tnks1bp1<em1(IMPC)J>/Tnks1bp1<em1(IMPC)J>	C57BL/6NJ-Tnks1bp1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394397	F	MP:0005419	decreased circulating serum albumin level	Tnks1bp1<em1(IMPC)J>/Tnks1bp1<em1(IMPC)J>	C57BL/6NJ-Tnks1bp1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394399	F	MP:0010123	increased bone mineral content	Tns3<em1(IMPC)Bay>/Tns3<+>	C57BL/6N-Tns3<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394399	M	MP:0000432	abnormal head morphology	Tns3<em1(IMPC)Bay>/Tns3<+>	C57BL/6N-Tns3<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394399	F	MP:0005140	decreased cardiac muscle contractility	Tns3<em1(IMPC)Bay>/Tns3<+>	C57BL/6N-Tns3<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394399	M	MP:0013279	increased fasting circulating glucose level	Tns3<em1(IMPC)Bay>/Tns3<+>	C57BL/6N-Tns3<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394399	F	MP:0000062	increased bone mineral density	Tns3<em1(IMPC)Bay>/Tns3<+>	C57BL/6N-Tns3<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6394401	F	MP:0003717	pallor	Trf<em1(IMPC)J>/Trf<em1(IMPC)J>	C57BL/6NJ-Trf<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394405	M	MP:0010024	increased total body fat amount	Ttc7<em1(IMPC)J>/Ttc7<+>	C57BL/6NJ-Ttc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394405	M	MP:0003961	decreased lean body mass	Ttc7<em1(IMPC)J>/Ttc7<+>	C57BL/6NJ-Ttc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394405	M	MP:0000367	abnormal coat/ hair morphology	Ttc7<em1(IMPC)J>/Ttc7<+>	C57BL/6NJ-Ttc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394405	F	MP:0010053	decreased grip strength	Ttc7<em1(IMPC)J>/Ttc7<+>	C57BL/6NJ-Ttc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394407	F	MP:0001399	hyperactivity	Tuba8<em1(IMPC)J>/Tuba8<em1(IMPC)J>	C57BL/6NJ-Tuba8<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394407	F	MP:0004122	abnormal sinus arrhythmia	Tuba8<em1(IMPC)J>/Tuba8<em1(IMPC)J>	C57BL/6NJ-Tuba8<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394407	M	MP:0003929	decreased heart rate variability	Tuba8<em1(IMPC)J>/Tuba8<em1(IMPC)J>	C57BL/6NJ-Tuba8<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394407	M	MP:0002075	abnormal coat/hair pigmentation	Tuba8<em1(IMPC)J>/Tuba8<em1(IMPC)J>	C57BL/6NJ-Tuba8<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394408	M	MP:0001406	abnormal gait	Tubb2a<em1(IMPC)J>/Tubb2a<em1(IMPC)J>	C57BL/6NJ-Tubb2a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394408	F	MP:0001399	hyperactivity	Tubb2a<em1(IMPC)J>/Tubb2a<em1(IMPC)J>	C57BL/6NJ-Tubb2a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394408	M	MP:0010053	decreased grip strength	Tubb2a<em1(IMPC)J>/Tubb2a<em1(IMPC)J>	C57BL/6NJ-Tubb2a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394409	M	MP:0011110	preweaning lethality, incomplete penetrance	Tubb4b<em1(IMPC)J>/Tubb4b<em1(IMPC)J>	C57BL/6NJ-Tubb4b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394410	M	MP:0001399	hyperactivity	Ubap2<em1(IMPC)J>/Ubap2<em1(IMPC)J>	C57BL/6NJ-Ubap2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394410	F	MP:0005566	decreased blood urea nitrogen level	Ubap2<em1(IMPC)J>/Ubap2<em1(IMPC)J>	C57BL/6NJ-Ubap2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394416	F	MP:0001297	microphthalmia	Vps26c<em1(IMPC)J>/Vps26c<em1(IMPC)J>	C57BL/6NJ-Vps26c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394416	F	MP:0000603	pale liver	Vps26c<em1(IMPC)J>/Vps26c<em1(IMPC)J>	C57BL/6NJ-Vps26c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394417	F	MP:0001314	cornea opacity	Vwa5a<em1(IMPC)J>/Vwa5a<em1(IMPC)J>	C57BL/6NJ-Vwa5a<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394419	F	MP:0000208	decreased hematocrit	Wdr24<tm1b(KOMP)Mbp>/Wdr24<+>	C57BL/6N-Wdr24<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6394419	M	MP:0010053	decreased grip strength	Wdr24<tm1b(KOMP)Mbp>/Wdr24<+>	C57BL/6N-Wdr24<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6394420	M	MP:0011874	enlarged urinary bladder	Dync2i1<em1(IMPC)Tcp>/Dync2i1<+>	C57BL/6NCrl-Dync2i1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394420	M	MP:0000470	abnormal stomach morphology	Dync2i1<em1(IMPC)Tcp>/Dync2i1<+>	C57BL/6NCrl-Dync2i1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6394421	F	MP:0010053	decreased grip strength	Wdr81<em1(IMPC)J>/Wdr81<+>	C57BL/6NJ-Wdr81<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394421	M	MP:0005565	increased blood urea nitrogen level	Wdr81<em1(IMPC)J>/Wdr81<+>	C57BL/6NJ-Wdr81<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394422	F	MP:0001566	increased circulating phosphate level	Wwp1<em1(IMPC)H>/Wwp1<em1(IMPC)H>	C57BL/6N-Wwp1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394422	M	MP:0001402	decreased locomotor activity	Wwp1<em1(IMPC)H>/Wwp1<em1(IMPC)H>	C57BL/6N-Wwp1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394422	M	MP:0013278	decreased fasting circulating glucose level	Wwp1<em1(IMPC)H>/Wwp1<em1(IMPC)H>	C57BL/6N-Wwp1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394422	M	MP:0002764	short tibia	Wwp1<em1(IMPC)H>/Wwp1<em1(IMPC)H>	C57BL/6N-Wwp1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6394423	F	MP:0003795	abnormal bone structure	Xkr4<em1(IMPC)J>/Xkr4<em1(IMPC)J>	C57BL/6NJ-Xkr4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394423	F	MP:0001417	decreased exploration in new environment	Xkr4<em1(IMPC)J>/Xkr4<em1(IMPC)J>	C57BL/6NJ-Xkr4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394426	M	MP:0003984	embryonic growth retardation	Zc3h13<em1(IMPC)J>/Zc3h13<em1(IMPC)J>	C57BL/6NJ-Zc3h13<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6394427	F	MP:0001258	decreased body length	Zfp174<em1(IMPC)J>/Zfp174<em1(IMPC)J>	C57BL/6NJ-Zfp174<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394427	M	MP:0001486	abnormal startle reflex	Zfp174<em1(IMPC)J>/Zfp174<em1(IMPC)J>	C57BL/6NJ-Zfp174<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394427	F	MP:0002111	abnormal tail morphology	Zfp174<em1(IMPC)J>/Zfp174<em1(IMPC)J>	C57BL/6NJ-Zfp174<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394428	M	MP:0002135	abnormal kidney morphology	Zfp503<em1(IMPC)Mbp>/Zfp503<+>	C57BL/6N-Zfp503<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394428	F	MP:0010053	decreased grip strength	Zfp503<em1(IMPC)Mbp>/Zfp503<+>	C57BL/6N-Zfp503<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394428	M	MP:0005554	decreased circulating creatinine level	Zfp503<em1(IMPC)Mbp>/Zfp503<+>	C57BL/6N-Zfp503<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394428	M	MP:0003068	enlarged kidney	Zfp503<em1(IMPC)Mbp>/Zfp503<+>	C57BL/6N-Zfp503<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394428	F	MP:0005560	decreased circulating glucose level	Zfp503<em1(IMPC)Mbp>/Zfp503<+>	C57BL/6N-Zfp503<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394428	F	MP:0002606	increased basophil cell number	Zfp503<em1(IMPC)Mbp>/Zfp503<+>	C57BL/6N-Zfp503<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394428	M	MP:0001415	increased exploration in new environment	Zfp503<em1(IMPC)Mbp>/Zfp503<+>	C57BL/6N-Zfp503<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6394429	M	MP:0002965	increased circulating serum albumin level	Zfp579<em1(IMPC)J>/Zfp579<em1(IMPC)J>	C57BL/6NJ-Zfp579<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394429	M	MP:0005568	increased circulating total protein level	Zfp579<em1(IMPC)J>/Zfp579<em1(IMPC)J>	C57BL/6NJ-Zfp579<em1(IMPC)J>/J	N	MGI:5576271
MGI:6394431	F	MP:0002833	increased heart weight	Zkscan17<tm1b(EUCOMM)Wtsi>/Zkscan17<+>	C57BL/6N-Zkscan17<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6394431	M	MP:0003179	thrombocytopenia	Zkscan17<tm1b(EUCOMM)Wtsi>/Zkscan17<+>	C57BL/6N-Zkscan17<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6399924	F	MP:0001447	abnormal nest building behavior	Shank3<tm2.1Bux>/Shank3<+>	B6(Cg)-Shank3<tm2.1Bux>	N	30302388
MGI:6399961	M	MP:0001155	arrest of spermatogenesis	Bard1<tm1.1Rjbr>/Bard1<tm1.1Rjbr>	involves: 129S6/SvEvTac * C57BL/6J	N	30244837
MGI:6399961	M	MP:0001147	small testis	Bard1<tm1.1Rjbr>/Bard1<tm1.1Rjbr>	involves: 129S6/SvEvTac * C57BL/6J	N	30244837
MGI:6399961	M	MP:0004901	decreased male germ cell number	Bard1<tm1.1Rjbr>/Bard1<tm1.1Rjbr>	involves: 129S6/SvEvTac * C57BL/6J	N	30244837
MGI:6399961	M	MP:0001925	male infertility	Bard1<tm1.1Rjbr>/Bard1<tm1.1Rjbr>	involves: 129S6/SvEvTac * C57BL/6J	N	30244837
MGI:6399962	M	MP:0001147	small testis	Bard1<tm2.1Rjbr>/Bard1<tm2.1Rjbr>	involves: 129S6/SvEvTac * C57BL/6J	N	30244837
MGI:6399962	M	MP:0001155	arrest of spermatogenesis	Bard1<tm2.1Rjbr>/Bard1<tm2.1Rjbr>	involves: 129S6/SvEvTac * C57BL/6J	N	30244837
MGI:6399962	M	MP:0004901	decreased male germ cell number	Bard1<tm2.1Rjbr>/Bard1<tm2.1Rjbr>	involves: 129S6/SvEvTac * C57BL/6J	N	30244837
MGI:6399962	M	MP:0001925	male infertility	Bard1<tm2.1Rjbr>/Bard1<tm2.1Rjbr>	involves: 129S6/SvEvTac * C57BL/6J	N	30244837
MGI:6400224	M	MP:0002896	abnormal bone mineralization	Notch3<em1Ecan>/Notch3<+>	C57BL/6J-Notch3<em1Ecan>	N	30042232
MGI:6400224	M	MP:0004984	increased osteoclast cell number	Notch3<em1Ecan>/Notch3<+>	C57BL/6J-Notch3<em1Ecan>	N	30042232
MGI:6400224	M	MP:0020039	increased bone ossification	Notch3<em1Ecan>/Notch3<+>	C57BL/6J-Notch3<em1Ecan>	N	30042232
MGI:6400710	M	MP:0001405	impaired coordination	Htt<tm5Detl>/Htt<+>	involves: C57BL/6	N	28927719
MGI:6400710	F	MP:0002797	increased thigmotaxis	Htt<tm5Detl>/Htt<+>	involves: C57BL/6	N	28927719
MGI:6400710	M	MP:0002804	abnormal motor learning	Htt<tm5Detl>/Htt<+>	involves: C57BL/6	N	28927719
MGI:6400710	F	MP:0001505	hunched posture	Htt<tm5Detl>/Htt<+>	involves: C57BL/6	N	28927719
MGI:6400710	M	MP:0010540	long stride length	Htt<tm5Detl>/Htt<+>	involves: C57BL/6	N	28927719
MGI:6400930	F	MP:0012575	increased noradrenaline level	Tafa1<tm1(KOMP)Vlcg>/Tafa1<tm1(KOMP)Vlcg>	C57BL/6N-Tafa1<tm1(KOMP)Vlcg>	N	31689372
MGI:6400930	F	MP:0020422	decreased freezing behavior	Tafa1<tm1(KOMP)Vlcg>/Tafa1<tm1(KOMP)Vlcg>	C57BL/6N-Tafa1<tm1(KOMP)Vlcg>	N	31689372
MGI:6400930	F	MP:0008965	increased basal metabolism	Tafa1<tm1(KOMP)Vlcg>/Tafa1<tm1(KOMP)Vlcg>	C57BL/6N-Tafa1<tm1(KOMP)Vlcg>	N	31689372
MGI:6400930	M	MP:0011945	increased eating frequency	Tafa1<tm1(KOMP)Vlcg>/Tafa1<tm1(KOMP)Vlcg>	C57BL/6N-Tafa1<tm1(KOMP)Vlcg>	N	31689372
MGI:6400930	M	MP:0005378	growth/size/body region phenotype	Tafa1<tm1(KOMP)Vlcg>/Tafa1<tm1(KOMP)Vlcg>	C57BL/6N-Tafa1<tm1(KOMP)Vlcg>	Y	31689372
MGI:6400930	F	MP:0001973	increased thermal nociceptive threshold	Tafa1<tm1(KOMP)Vlcg>/Tafa1<tm1(KOMP)Vlcg>	C57BL/6N-Tafa1<tm1(KOMP)Vlcg>	N	31689372
MGI:6400930	F	MP:0020874	abnormal nervous system dopamine level	Tafa1<tm1(KOMP)Vlcg>/Tafa1<tm1(KOMP)Vlcg>	C57BL/6N-Tafa1<tm1(KOMP)Vlcg>	N	31689372
MGI:6400930	F	MP:0001364	decreased anxiety-related response	Tafa1<tm1(KOMP)Vlcg>/Tafa1<tm1(KOMP)Vlcg>	C57BL/6N-Tafa1<tm1(KOMP)Vlcg>	N	31689372
MGI:6400930	M	MP:0011940	decreased food intake	Tafa1<tm1(KOMP)Vlcg>/Tafa1<tm1(KOMP)Vlcg>	C57BL/6N-Tafa1<tm1(KOMP)Vlcg>	N	31689372
MGI:6400930	M	MP:0005376	homeostasis/metabolism phenotype	Tafa1<tm1(KOMP)Vlcg>/Tafa1<tm1(KOMP)Vlcg>	C57BL/6N-Tafa1<tm1(KOMP)Vlcg>	Y	31689372
MGI:6400930	F	MP:0004889	increased energy expenditure	Tafa1<tm1(KOMP)Vlcg>/Tafa1<tm1(KOMP)Vlcg>	C57BL/6N-Tafa1<tm1(KOMP)Vlcg>	N	31689372
MGI:6400930	M	MP:0011939	increased food intake	Tafa1<tm1(KOMP)Vlcg>/Tafa1<tm1(KOMP)Vlcg>	C57BL/6N-Tafa1<tm1(KOMP)Vlcg>	N	31689372
MGI:6401062	M	MP:0001973	increased thermal nociceptive threshold	Hpcal4<tm1(KOMP)Vlcg>/Hpcal4<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	32015563
MGI:6401160	M	MP:0001501	abnormal sleep pattern	Gria3<em1Wthg>/Y	C57BL/6-Gria3<em1Wthg>	N	29016847
MGI:6401160	M	MP:0004753	abnormal miniature excitatory postsynaptic currents	Gria3<em1Wthg>/Y	C57BL/6-Gria3<em1Wthg>	N	29016847
MGI:6401803	F	MP:0001923	reduced female fertility	Nlrp4f<em1Lil>/Nlrp4f<em1Lil>	involves: CD-1	N	31575650
MGI:6401803	F	MP:0001935	decreased litter size	Nlrp4f<em1Lil>/Nlrp4f<em1Lil>	involves: CD-1	N	31575650
MGI:6401803	F	MP:0001125	abnormal oocyte morphology	Nlrp4f<em1Lil>/Nlrp4f<em1Lil>	involves: CD-1	N	31575650
MGI:6402203	F	MP:0008247	abnormal mononuclear cell morphology	Tg(KRT18-DPP4)3Pbmj/0	involves: C57BL/6J * SJL/J	N	29152574
MGI:6402203	F	MP:0000488	abnormal intestinal epithelium morphology	Tg(KRT18-DPP4)3Pbmj/0	involves: C57BL/6J * SJL/J	N	29152574
MGI:6402203	F	MP:0001861	lung inflammation	Tg(KRT18-DPP4)3Pbmj/0	involves: C57BL/6J * SJL/J	N	29152574
MGI:6402203	F	MP:0001862	interstitial pneumonia	Tg(KRT18-DPP4)3Pbmj/0	involves: C57BL/6J * SJL/J	N	29152574
MGI:6402203	F	MP:0020949	increased susceptibility to Coronaviridae infection	Tg(KRT18-DPP4)3Pbmj/0	involves: C57BL/6J * SJL/J	N	29152574
MGI:6402203	F	MP:0005013	increased lymphocyte cell number	Tg(KRT18-DPP4)3Pbmj/0	involves: C57BL/6J * SJL/J	N	29152574
MGI:6402203	F	MP:0000496	abnormal small intestine morphology	Tg(KRT18-DPP4)3Pbmj/0	involves: C57BL/6J * SJL/J	N	29152574
MGI:6402203	F	MP:0008108	abnormal small intestinal villus morphology	Tg(KRT18-DPP4)3Pbmj/0	involves: C57BL/6J * SJL/J	N	29152574
MGI:6402203	F	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality	Tg(KRT18-DPP4)3Pbmj/0	involves: C57BL/6J * SJL/J	N	29152574
MGI:6402529	F	MP:0012041	increased susceptibility to pulmonary hyaline membrane formation	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	16001071
MGI:6402529	F	MP:0001861	lung inflammation	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	31645418
MGI:6402529	F	MP:0010180	increased susceptibility to weight loss	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	31645418
MGI:6402529	F	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	16001071
MGI:6402529	F	MP:0005165	increased susceptibility to injury	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	16001071
MGI:6402529	F	MP:0031229	increased angiotensin II level	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	16001071
MGI:6402529	F	MP:0011044	increased lung elastance	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	16001071
MGI:6402529	F	MP:0003828	pulmonary edema	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	16001071
MGI:6402529	F	MP:0001861	lung inflammation	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	16001071
MGI:6402529	F	MP:0031232	increased circulating angiotensin II level	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	16001071
MGI:6402529	F	MP:0002412	increased susceptibility to bacterial infection	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	31645418
MGI:6402529	F	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	31645418
MGI:6402529	F	MP:0000219	increased neutrophil cell number	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	31645418
MGI:6402529	F	MP:0003070	increased vascular permeability	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd	N	16001071
MGI:6402530	M	MP:0002412	increased susceptibility to bacterial infection	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	31645418
MGI:6402530	M	MP:0011044	increased lung elastance	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	16001071
MGI:6402530	M	MP:0005165	increased susceptibility to injury	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	16001071
MGI:6402530	M	MP:0031232	increased circulating angiotensin II level	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	16001071
MGI:6402530	M	MP:0031229	increased angiotensin II level	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	16001071
MGI:6402530	M	MP:0003070	increased vascular permeability	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	16001071
MGI:6402530	M	MP:0010180	increased susceptibility to weight loss	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	31645418
MGI:6402530	M	MP:0001861	lung inflammation	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	31645418
MGI:6402530	M	MP:0001861	lung inflammation	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	16001071
MGI:6402530	M	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	16001071
MGI:6402530	M	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	31645418
MGI:6402530	M	MP:0012041	increased susceptibility to pulmonary hyaline membrane formation	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	16001071
MGI:6402530	M	MP:0003828	pulmonary edema	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	16001071
MGI:6402530	M	MP:0000219	increased neutrophil cell number	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd	N	31645418
MGI:6402560	M	MP:0005165	increased susceptibility to injury	Agtr2<tm1Gsb>/Y	involves: 129S1/Sv * 129X1/SvJ	N	16001071
MGI:6402565	F	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6J	N	24800825
MGI:6402565	F	MP:0003828	pulmonary edema	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6J	N	24800825
MGI:6402565	F	MP:0001861	lung inflammation	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6J	N	24800825
MGI:6402565	F	MP:0020946	increased susceptibility to Orthomyxoviridae infection	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6J	N	24800825
MGI:6402565	F	MP:0012041	increased susceptibility to pulmonary hyaline membrane formation	Ace2<tm1Pngr>/Ace2<tm1Pngr>	involves: 129P2/OlaHsd * C57BL/6J	N	24800825
MGI:6402568	M	MP:0003828	pulmonary edema	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	24800825
MGI:6402568	M	MP:0020946	increased susceptibility to Orthomyxoviridae infection	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	24800825
MGI:6402568	M	MP:0012041	increased susceptibility to pulmonary hyaline membrane formation	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	24800825
MGI:6402568	M	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	24800825
MGI:6402568	M	MP:0001861	lung inflammation	Ace2<tm1Pngr>/Y	involves: 129P2/OlaHsd * C57BL/6J	N	24800825
MGI:6402817	F	MP:0014142	increased body fat mass	Otp<M1H>/Otp<+>	C3H.Cg-Otp<M1H>	N	29107289
MGI:6402817	F	MP:0005331	insulin resistance	Otp<M1H>/Otp<+>	C3H.Cg-Otp<M1H>	N	29107289
MGI:6402817	F	MP:0005293	impaired glucose tolerance	Otp<M1H>/Otp<+>	C3H.Cg-Otp<M1H>	N	29107289
MGI:6402817	F	MP:0001261	obese	Otp<M1H>/Otp<+>	C3H.Cg-Otp<M1H>	N	29107289
MGI:6402817	M	MP:0001261	obese	Otp<M1H>/Otp<+>	C3H.Cg-Otp<M1H>	N	29107289
MGI:6402817	F	MP:0002079	increased circulating insulin level	Otp<M1H>/Otp<+>	C3H.Cg-Otp<M1H>	N	29107289
MGI:6402817	F	MP:0005669	increased circulating leptin level	Otp<M1H>/Otp<+>	C3H.Cg-Otp<M1H>	N	29107289
MGI:6402817	M	MP:0005448	abnormal energy homeostasis	Otp<M1H>/Otp<+>	C3H.Cg-Otp<M1H>	N	29107289
MGI:6402817	F	MP:0003960	increased lean body mass	Otp<M1H>/Otp<+>	C3H.Cg-Otp<M1H>	N	29107289
MGI:6402819	F	MP:0003960	increased lean body mass	Otp<tm1Asim>/Otp<+>	C3H.129P2(B6)-Otp<tm1Asim>	N	29107289
MGI:6402819	F	MP:0014142	increased body fat mass	Otp<tm1Asim>/Otp<+>	C3H.129P2(B6)-Otp<tm1Asim>	N	29107289
MGI:6402819	F	MP:0005331	insulin resistance	Otp<tm1Asim>/Otp<+>	C3H.129P2(B6)-Otp<tm1Asim>	N	29107289
MGI:6402819	M	MP:0005331	insulin resistance	Otp<tm1Asim>/Otp<+>	C3H.129P2(B6)-Otp<tm1Asim>	N	29107289
MGI:6402819	M	MP:0003960	increased lean body mass	Otp<tm1Asim>/Otp<+>	C3H.129P2(B6)-Otp<tm1Asim>	N	29107289
MGI:6402819	M	MP:0014142	increased body fat mass	Otp<tm1Asim>/Otp<+>	C3H.129P2(B6)-Otp<tm1Asim>	N	29107289
MGI:6402902	F	MP:0001926	female infertility	1700028K03Rik<em1Jzc>/1700028K03Rik<em1Jzc>	C57BL/6-1700028K03Rik<em1Jzc>	N	30949703
MGI:6402902	F	MP:0005431	decreased oocyte number	1700028K03Rik<em1Jzc>/1700028K03Rik<em1Jzc>	C57BL/6-1700028K03Rik<em1Jzc>	N	30949703
MGI:6402902	F	MP:0001127	small ovary	1700028K03Rik<em1Jzc>/1700028K03Rik<em1Jzc>	C57BL/6-1700028K03Rik<em1Jzc>	N	30949703
MGI:6402902	M	MP:0014052	increased male germ cell apoptosis	1700028K03Rik<em1Jzc>/1700028K03Rik<em1Jzc>	C57BL/6-1700028K03Rik<em1Jzc>	N	30949703
MGI:6402902	M	MP:0001147	small testis	1700028K03Rik<em1Jzc>/1700028K03Rik<em1Jzc>	C57BL/6-1700028K03Rik<em1Jzc>	N	30949703
MGI:6402902	F	MP:0010767	abnormal female meiosis I arrest	1700028K03Rik<em1Jzc>/1700028K03Rik<em1Jzc>	C57BL/6-1700028K03Rik<em1Jzc>	N	30949703
MGI:6402902	F	MP:0004805	absent oocytes	1700028K03Rik<em1Jzc>/1700028K03Rik<em1Jzc>	C57BL/6-1700028K03Rik<em1Jzc>	N	30949703
MGI:6402902	M	MP:0001925	male infertility	1700028K03Rik<em1Jzc>/1700028K03Rik<em1Jzc>	C57BL/6-1700028K03Rik<em1Jzc>	N	30949703
MGI:6402902	M	MP:0005159	azoospermia	1700028K03Rik<em1Jzc>/1700028K03Rik<em1Jzc>	C57BL/6-1700028K03Rik<em1Jzc>	N	30949703
MGI:6402902	M	MP:0008261	arrest of male meiosis	1700028K03Rik<em1Jzc>/1700028K03Rik<em1Jzc>	C57BL/6-1700028K03Rik<em1Jzc>	N	30949703
MGI:6403997	M	MP:0012335	increased circulating homocysteine level	Chdh<em1Rmps>/Chdh<em1Rmps>	C57BL/6N-Chdh<em1Rmps>	N	31255657
MGI:6403997	M	MP:0005370	liver/biliary system phenotype	Chdh<em1Rmps>/Chdh<em1Rmps>	C57BL/6N-Chdh<em1Rmps>	Y	31255657
MGI:6403997	M	MP:0021134	decreased amino acid betaine level	Chdh<em1Rmps>/Chdh<em1Rmps>	C57BL/6N-Chdh<em1Rmps>	N	31255657
MGI:6403997	M	MP:0003360	abnormal depression-related behavior	Chdh<em1Rmps>/Chdh<em1Rmps>	C57BL/6N-Chdh<em1Rmps>	N	31255657
MGI:6404038	F	MP:0001125	abnormal oocyte morphology	Kdm3b<tm1Jxu>/Kdm3b<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	25892958
MGI:6404038	F	MP:0003699	abnormal female reproductive system physiology	Kdm3b<tm1Jxu>/Kdm3b<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	25892958
MGI:6404038	F	MP:0009006	prolonged estrous cycle	Kdm3b<tm1Jxu>/Kdm3b<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	25892958
MGI:6404038	F	MP:0001729	impaired embryo implantation	Kdm3b<tm1Jxu>/Kdm3b<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	25892958
MGI:6404038	F	MP:0003355	decreased ovulation rate	Kdm3b<tm1Jxu>/Kdm3b<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	25892958
MGI:6404038	F	MP:0003845	abnormal decidualization	Kdm3b<tm1Jxu>/Kdm3b<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	25892958
MGI:6404038	F	MP:0005181	decreased circulating estradiol level	Kdm3b<tm1Jxu>/Kdm3b<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	25892958
MGI:6404038	F	MP:0009661	abnormal pregnancy	Kdm3b<tm1Jxu>/Kdm3b<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	25892958
MGI:6404038	F	MP:0001926	female infertility	Kdm3b<tm1Jxu>/Kdm3b<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	25892958
MGI:6404038	F	MP:0005389	reproductive system phenotype	Kdm3b<tm1Jxu>/Kdm3b<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	Y	25892958
MGI:6404038	F	MP:0009011	prolonged diestrus	Kdm3b<tm1Jxu>/Kdm3b<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	25892958
MGI:6404038	F	MP:0009647	decreased fertilization frequency	Kdm3b<tm1Jxu>/Kdm3b<tm1Jxu>	involves: 129S6/SvEvTac * C57BL/6	N	25892958
MGI:6404118	M	MP:0008158	increased diameter of femur	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	N	28477420
MGI:6404118	M	MP:0009642	abnormal blood homeostasis	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	N	28477420
MGI:6404118	M	MP:0020039	increased bone ossification	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	N	28477420
MGI:6404118	M	MP:0010878	increased trabecular bone volume	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	N	28477420
MGI:6404118	M	MP:0005369	muscle phenotype	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	Y	28477420
MGI:6404118	M	MP:0013623	increased femur compact bone thickness	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	N	28477420
MGI:6404118	M	MP:0010932	increased trabecular bone connectivity density	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	N	28477420
MGI:6404118	M	MP:0004149	increased bone strength	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	N	28477420
MGI:6404118	M	MP:0005390	skeleton phenotype	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	Y	28477420
MGI:6404118	M	MP:0010868	increased bone trabecula number	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	N	28477420
MGI:6404118	M	MP:0030278	thick neurocranium	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	N	28477420
MGI:6404118	M	MP:0013631	decreased bone trabecular spacing	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	N	28477420
MGI:6404118	M	MP:0009347	increased trabecular bone thickness	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	N	28477420
MGI:6404118	M	MP:0008753	abnormal osteocyte morphology	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	N	28477420
MGI:6404118	M	MP:0005367	renal/urinary system phenotype	Lrp4<tm1.1Pg>/Lrp4<tm1.1Pg>	involves: C57BL/6N	Y	28477420
MGI:6404124	F	MP:0001935	decreased litter size	Leat1<Tg(Tyr)442Ove>/Leat1<Tg(Tyr)442Ove>	FVB/NJ-Leat1<Tg(Tyr)442Ove>	N	31830612
MGI:6404124	F	MP:0003718	maternal effect	Leat1<Tg(Tyr)442Ove>/Leat1<Tg(Tyr)442Ove>	FVB/NJ-Leat1<Tg(Tyr)442Ove>	N	31830612
MGI:6404124	F	MP:0003550	short perineum	Leat1<Tg(Tyr)442Ove>/Leat1<Tg(Tyr)442Ove>	FVB/NJ-Leat1<Tg(Tyr)442Ove>	N	31830612
MGI:6404124	F	MP:0001923	reduced female fertility	Leat1<Tg(Tyr)442Ove>/Leat1<Tg(Tyr)442Ove>	FVB/NJ-Leat1<Tg(Tyr)442Ove>	N	31830612
MGI:6404125	M	MP:0004149	increased bone strength	Lrp4<tm1.1Pg>/Lrp4<+>	involves: C57BL/6N	N	28477420
MGI:6404225	F	MP:0001262	decreased body weight	Neb<m2Anu>/Neb<+>	C57BL/6J-Neb<m2Anu>	N	32066503
MGI:6404227	F	MP:0001265	decreased body size	Neb<m1Anu>/Neb<m2Anu>	C57BL/6J-Neb<m1Anu> Neb<m2Anu>	N	32066503
MGI:6404227	F	MP:0010053	decreased grip strength	Neb<m1Anu>/Neb<m2Anu>	C57BL/6J-Neb<m1Anu> Neb<m2Anu>	N	32066503
MGI:6404227	F	MP:0001402	decreased locomotor activity	Neb<m1Anu>/Neb<m2Anu>	C57BL/6J-Neb<m1Anu> Neb<m2Anu>	N	32066503
MGI:6404451	F	MP:0001935	decreased litter size	Ezhip<em1Marg>/Ezhip<em1Marg>	involves: C57BL/6N	N	31451685
MGI:6404451	F	MP:0001127	small ovary	Ezhip<em1Marg>/Ezhip<em1Marg>	involves: C57BL/6N	N	31451685
MGI:6404451	F	MP:0004856	decreased ovary weight	Ezhip<em1Marg>/Ezhip<em1Marg>	involves: C57BL/6N	N	31451685
MGI:6404451	F	MP:0001923	reduced female fertility	Ezhip<em1Marg>/Ezhip<em1Marg>	involves: C57BL/6N	N	31451685
MGI:6404451	F	MP:0011121	decreased primordial ovarian follicle number	Ezhip<em1Marg>/Ezhip<em1Marg>	involves: C57BL/6N	N	31451685
MGI:6404451	F	MP:0008995	early reproductive senescence	Ezhip<em1Marg>/Ezhip<em1Marg>	involves: C57BL/6N	N	31451685
MGI:6404452	M	MP:0005389	reproductive system phenotype	Ezhip<em1Marg>/Y	involves: C57BL/6N	Y	31451685
MGI:6404457	M	MP:0004215	abnormal myocardial fiber physiology	Pcca<tm1Tmiy>/Pcca<tm1Tmiy>,Tg(CAG-PCCA*A138T,-EGFP)#Maba/0	involves: 129P2/OlaHsd * FVB/N	N	31678161
MGI:6404457	M	MP:0003674	oxidative stress	Pcca<tm1Tmiy>/Pcca<tm1Tmiy>,Tg(CAG-PCCA*A138T,-EGFP)#Maba/0	involves: 129P2/OlaHsd * FVB/N	N	31678161
MGI:6404457	M	MP:0005140	decreased cardiac muscle contractility	Pcca<tm1Tmiy>/Pcca<tm1Tmiy>,Tg(CAG-PCCA*A138T,-EGFP)#Maba/0	involves: 129P2/OlaHsd * FVB/N	N	31678161
MGI:6404457	M	MP:0012557	decreased calcium uptake by cardiac muscle	Pcca<tm1Tmiy>/Pcca<tm1Tmiy>,Tg(CAG-PCCA*A138T,-EGFP)#Maba/0	involves: 129P2/OlaHsd * FVB/N	N	31678161
MGI:6404457	M	MP:0009732	ventricular premature beat	Pcca<tm1Tmiy>/Pcca<tm1Tmiy>,Tg(CAG-PCCA*A138T,-EGFP)#Maba/0	involves: 129P2/OlaHsd * FVB/N	N	31678161
MGI:6404635	M	MP:0005386	behavior/neurological phenotype	Tardbp<tm2.1Ckjs>/Tardbp<tm2.1Ckjs>	involves: C57BL/6J	Y	31964415
MGI:6404636	M	MP:0001263	weight loss	Tardbp<tm3.1Ckjs>/Tardbp<+>	involves: C57BL/6J	N	31964415
MGI:6404636	M	MP:0009417	skeletal muscle atrophy	Tardbp<tm3.1Ckjs>/Tardbp<+>	involves: C57BL/6J	N	31964415
MGI:6404636	M	MP:0000755	hindlimb paralysis	Tardbp<tm3.1Ckjs>/Tardbp<+>	involves: C57BL/6J	N	31964415
MGI:6404636	M	MP:0001053	abnormal neuromuscular synapse morphology	Tardbp<tm3.1Ckjs>/Tardbp<+>	involves: C57BL/6J	N	31964415
MGI:6404636	M	MP:0011975	neuronal cytoplasmic inclusions	Tardbp<tm3.1Ckjs>/Tardbp<+>	involves: C57BL/6J	N	31964415
MGI:6404636	M	MP:0012051	spasticity	Tardbp<tm3.1Ckjs>/Tardbp<+>	involves: C57BL/6J	N	31964415
MGI:6404636	M	MP:0001513	limb grasping	Tardbp<tm3.1Ckjs>/Tardbp<+>	involves: C57BL/6J	N	31964415
MGI:6404636	M	MP:0001405	impaired coordination	Tardbp<tm3.1Ckjs>/Tardbp<+>	involves: C57BL/6J	N	31964415
MGI:6404636	M	MP:0003354	astrocytosis	Tardbp<tm3.1Ckjs>/Tardbp<+>	involves: C57BL/6J	N	31964415
MGI:6404636	M	MP:0000937	abnormal motor neuron morphology	Tardbp<tm3.1Ckjs>/Tardbp<+>	involves: C57BL/6J	N	31964415
MGI:6404636	M	MP:0000745	tremors	Tardbp<tm3.1Ckjs>/Tardbp<+>	involves: C57BL/6J	N	31964415
MGI:6404636	M	MP:0000160	kyphosis	Tardbp<tm3.1Ckjs>/Tardbp<+>	involves: C57BL/6J	N	31964415
MGI:6404636	M	MP:0000938	motor neuron degeneration	Tardbp<tm3.1Ckjs>/Tardbp<+>	involves: C57BL/6J	N	31964415
MGI:6404937	M	MP:0003727	abnormal retina layer morphology	Rs1<tm1.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404937	M	MP:0008515	thin retina outer nuclear layer	Rs1<tm1.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404937	M	MP:0012143	decreased a-wave amplitude	Rs1<tm1.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404937	M	MP:0004811	abnormal neuron physiology	Rs1<tm1.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404937	M	MP:0002184	abnormal innervation	Rs1<tm1.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404937	M	MP:0001325	abnormal retina morphology	Rs1<tm1.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404937	M	MP:0014333	short retina cone cell outer segment	Rs1<tm1.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404937	M	MP:0002182	abnormal astrocyte morphology	Rs1<tm1.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404937	M	MP:0005551	abnormal eye electrophysiology	Rs1<tm1.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404937	M	MP:0012144	decreased b-wave amplitude	Rs1<tm1.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404937	M	MP:0001006	abnormal retina cone cell morphology	Rs1<tm1.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404937	M	MP:0005547	abnormal Muller cell morphology	Rs1<tm1.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404937	M	MP:0012029	abnormal electroretinogram waveform feature	Rs1<tm1.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404946	M	MP:0001006	abnormal retina cone cell morphology	Rs1<tm2.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404946	M	MP:0004811	abnormal neuron physiology	Rs1<tm2.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404946	M	MP:0012144	decreased b-wave amplitude	Rs1<tm2.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404946	M	MP:0012029	abnormal electroretinogram waveform feature	Rs1<tm2.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404946	M	MP:0008515	thin retina outer nuclear layer	Rs1<tm2.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404946	M	MP:0002182	abnormal astrocyte morphology	Rs1<tm2.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404946	M	MP:0001325	abnormal retina morphology	Rs1<tm2.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404946	M	MP:0003727	abnormal retina layer morphology	Rs1<tm2.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404946	M	MP:0005551	abnormal eye electrophysiology	Rs1<tm2.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404946	M	MP:0002184	abnormal innervation	Rs1<tm2.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404946	M	MP:0005547	abnormal Muller cell morphology	Rs1<tm2.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404946	M	MP:0014333	short retina cone cell outer segment	Rs1<tm2.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404946	M	MP:0012143	decreased a-wave amplitude	Rs1<tm2.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404948	M	MP:0002182	abnormal astrocyte morphology	Rs1<tm3.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404948	M	MP:0012144	decreased b-wave amplitude	Rs1<tm3.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404948	M	MP:0004811	abnormal neuron physiology	Rs1<tm3.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404948	M	MP:0002184	abnormal innervation	Rs1<tm3.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404948	M	MP:0012029	abnormal electroretinogram waveform feature	Rs1<tm3.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404948	M	MP:0001006	abnormal retina cone cell morphology	Rs1<tm3.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404948	M	MP:0005547	abnormal Muller cell morphology	Rs1<tm3.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404948	M	MP:0014333	short retina cone cell outer segment	Rs1<tm3.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404948	M	MP:0003727	abnormal retina layer morphology	Rs1<tm3.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404948	M	MP:0005551	abnormal eye electrophysiology	Rs1<tm3.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404948	M	MP:0012143	decreased a-wave amplitude	Rs1<tm3.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404948	M	MP:0008515	thin retina outer nuclear layer	Rs1<tm3.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404948	M	MP:0001325	abnormal retina morphology	Rs1<tm3.1Rom>/Y	involves: 129S6/SvEvTac * C57BL/6NTac	N	31174210
MGI:6404952	F	MP:0005391	vision/eye phenotype	Rs1<tm2.1Rom>/Rs1<+>	involves: 129S6/SvEvTac * C57BL/6NTac	Y	31174210
MGI:6404954	F	MP:0005391	vision/eye phenotype	Rs1<tm3.1Rom>/Rs1<+>	involves: 129S6/SvEvTac * C57BL/6NTac	Y	31174210
MGI:6405042	M	MP:0001860	liver inflammation	Mc4r<tm1Matsu>/Mc4r<tm1Matsu>	C57BL/6J-Mc4r<tm1Matsu>	N	31990961
MGI:6405042	M	MP:0005178	increased circulating cholesterol level	Mc4r<tm1Matsu>/Mc4r<tm1Matsu>	C57BL/6J-Mc4r<tm1Matsu>	N	31990961
MGI:6405042	M	MP:0009355	increased liver triglyceride level	Mc4r<tm1Matsu>/Mc4r<tm1Matsu>	C57BL/6J-Mc4r<tm1Matsu>	N	31990961
MGI:6405042	M	MP:0002981	increased liver weight	Mc4r<tm1Matsu>/Mc4r<tm1Matsu>	C57BL/6J-Mc4r<tm1Matsu>	N	31990961
MGI:6405042	M	MP:0030678	increased hydroxyproline level	Mc4r<tm1Matsu>/Mc4r<tm1Matsu>	C57BL/6J-Mc4r<tm1Matsu>	N	31990961
MGI:6405042	M	MP:0005343	increased circulating aspartate transaminase level	Mc4r<tm1Matsu>/Mc4r<tm1Matsu>	C57BL/6J-Mc4r<tm1Matsu>	N	31990961
MGI:6405042	M	MP:0005658	increased susceptibility to diet-induced obesity	Mc4r<tm1Matsu>/Mc4r<tm1Matsu>	C57BL/6J-Mc4r<tm1Matsu>	N	31990961
MGI:6405042	M	MP:0003333	liver fibrosis	Mc4r<tm1Matsu>/Mc4r<tm1Matsu>	C57BL/6J-Mc4r<tm1Matsu>	N	31990961
MGI:6405042	M	MP:0002079	increased circulating insulin level	Mc4r<tm1Matsu>/Mc4r<tm1Matsu>	C57BL/6J-Mc4r<tm1Matsu>	N	31990961
MGI:6405042	M	MP:0002628	hepatic steatosis	Mc4r<tm1Matsu>/Mc4r<tm1Matsu>	C57BL/6J-Mc4r<tm1Matsu>	N	31990961
MGI:6405042	M	MP:0002941	increased circulating alanine transaminase level	Mc4r<tm1Matsu>/Mc4r<tm1Matsu>	C57BL/6J-Mc4r<tm1Matsu>	N	31990961
MGI:6405042	M	MP:0011939	increased food intake	Mc4r<tm1Matsu>/Mc4r<tm1Matsu>	C57BL/6J-Mc4r<tm1Matsu>	N	31990961
MGI:6407437	M	MP:0020234	decreased basal metabolism	Gt(ROSA)26Sor<tm1(CAG-LMNA*)Cyh>/Gt(ROSA)26Sor<+>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6JNarl * FVB	N	31833196
MGI:6407437	M	MP:0005534	decreased body temperature	Gt(ROSA)26Sor<tm1(CAG-LMNA*)Cyh>/Gt(ROSA)26Sor<+>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6JNarl * FVB	N	31833196
MGI:6407437	M	MP:0002970	abnormal white adipose tissue morphology	Gt(ROSA)26Sor<tm1(CAG-LMNA*)Cyh>/Gt(ROSA)26Sor<+>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6JNarl * FVB	N	31833196
MGI:6407437	M	MP:0001402	decreased locomotor activity	Gt(ROSA)26Sor<tm1(CAG-LMNA*)Cyh>/Gt(ROSA)26Sor<+>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6JNarl * FVB	N	31833196
MGI:6407437	M	MP:0014143	decreased body fat mass	Gt(ROSA)26Sor<tm1(CAG-LMNA*)Cyh>/Gt(ROSA)26Sor<+>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6JNarl * FVB	N	31833196
MGI:6407437	M	MP:0005290	decreased oxygen consumption	Gt(ROSA)26Sor<tm1(CAG-LMNA*)Cyh>/Gt(ROSA)26Sor<+>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6JNarl * FVB	N	31833196
MGI:6407437	M	MP:0010378	increased respiratory quotient	Gt(ROSA)26Sor<tm1(CAG-LMNA*)Cyh>/Gt(ROSA)26Sor<+>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6JNarl * FVB	N	31833196
MGI:6407437	M	MP:0008964	decreased carbon dioxide production	Gt(ROSA)26Sor<tm1(CAG-LMNA*)Cyh>/Gt(ROSA)26Sor<+>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6JNarl * FVB	N	31833196
MGI:6407437	M	MP:0005424	jerky movement	Gt(ROSA)26Sor<tm1(CAG-LMNA*)Cyh>/Gt(ROSA)26Sor<+>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6JNarl * FVB	N	31833196
MGI:6407437	M	MP:0010053	decreased grip strength	Gt(ROSA)26Sor<tm1(CAG-LMNA*)Cyh>/Gt(ROSA)26Sor<+>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6JNarl * FVB	N	31833196
MGI:6408212	M	MP:0002135	abnormal kidney morphology	1600029I14Rik<tm1b(KOMP)Wtsi>/1600029I14Rik<tm1b(KOMP)Wtsi>	C57BL/6N-1600029I14Rik<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6408212	M	MP:0004930	small epididymis	1600029I14Rik<tm1b(KOMP)Wtsi>/1600029I14Rik<tm1b(KOMP)Wtsi>	C57BL/6N-1600029I14Rik<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6408213	M	MP:0005534	decreased body temperature	1700016H13Rik<em1(IMPC)Bay>/1700016H13Rik<em1(IMPC)Bay>	C57BL/6N-1700016H13Rik<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408217	F	MP:0000639	abnormal adrenal gland morphology	2510009E07Rik<em1(IMPC)Ccpcz>/2510009E07Rik<em1(IMPC)Ccpcz>	C57BL/6N-2510009E07Rik<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408217	F	MP:0000642	enlarged adrenal glands	2510009E07Rik<em1(IMPC)Ccpcz>/2510009E07Rik<em1(IMPC)Ccpcz>	C57BL/6N-2510009E07Rik<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408217	M	MP:0000274	enlarged heart	2510009E07Rik<em1(IMPC)Ccpcz>/2510009E07Rik<em1(IMPC)Ccpcz>	C57BL/6N-2510009E07Rik<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408217	F	MP:0002135	abnormal kidney morphology	2510009E07Rik<em1(IMPC)Ccpcz>/2510009E07Rik<em1(IMPC)Ccpcz>	C57BL/6N-2510009E07Rik<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408217	F	MP:0000443	abnormal snout morphology	2510009E07Rik<em1(IMPC)Ccpcz>/2510009E07Rik<em1(IMPC)Ccpcz>	C57BL/6N-2510009E07Rik<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408217	F	MP:0003068	enlarged kidney	2510009E07Rik<em1(IMPC)Ccpcz>/2510009E07Rik<em1(IMPC)Ccpcz>	C57BL/6N-2510009E07Rik<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408217	F	MP:0000367	abnormal coat/ hair morphology	2510009E07Rik<em1(IMPC)Ccpcz>/2510009E07Rik<em1(IMPC)Ccpcz>	C57BL/6N-2510009E07Rik<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408217	M	MP:0000266	abnormal heart morphology	2510009E07Rik<em1(IMPC)Ccpcz>/2510009E07Rik<em1(IMPC)Ccpcz>	C57BL/6N-2510009E07Rik<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408218	M	MP:0000063	decreased bone mineral density	Lyz3<tm1(KOMP)Vlcg>/Lyz3<tm1(KOMP)Vlcg>	C57BL/6N-Lyz3<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408218	F	MP:0001257	increased body length	Lyz3<tm1(KOMP)Vlcg>/Lyz3<tm1(KOMP)Vlcg>	C57BL/6N-Lyz3<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408218	F	MP:0002941	increased circulating alanine transaminase level	Lyz3<tm1(KOMP)Vlcg>/Lyz3<tm1(KOMP)Vlcg>	C57BL/6N-Lyz3<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408218	F	MP:0005343	increased circulating aspartate transaminase level	Lyz3<tm1(KOMP)Vlcg>/Lyz3<tm1(KOMP)Vlcg>	C57BL/6N-Lyz3<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408220	M	MP:0002874	decreased hemoglobin content	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	M	MP:0005553	increased circulating creatinine level	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	M	MP:0005634	decreased circulating sodium level	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	F	MP:0013510	decreased CD4-negative NK T cell number	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	F	MP:0005627	increased circulating potassium level	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	F	MP:0001303	abnormal lens morphology	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	M	MP:0005343	increased circulating aspartate transaminase level	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	M	MP:0001523	impaired righting response	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	F	MP:0005278	abnormal cholesterol homeostasis	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	M	MP:0004151	decreased circulating iron level	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	M	MP:0000208	decreased hematocrit	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	F	MP:0011044	increased lung elastance	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	F	MP:0001926	female infertility	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	M	MP:0008207	decreased B-2 B cell number	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	M	MP:0002591	decreased mean corpuscular volume	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408220	M	MP:0001925	male infertility	Abcg8<tm1b(KOMP)Wtsi>/Abcg8<tm1b(KOMP)Wtsi>	C57BL/6N-Abcg8<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408221	M	MP:0002079	increased circulating insulin level	Acad12<tm1b(EUCOMM)Wtsi>/Acad12<tm1b(EUCOMM)Wtsi>	C57BL/6N-Acad12<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408222	F	MP:0000266	abnormal heart morphology	Ache<em1(IMPC)Mbp>/Ache<+>	C57BL/6N-Ache<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408222	F	MP:0002188	small heart	Ache<em1(IMPC)Mbp>/Ache<+>	C57BL/6N-Ache<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408222	M	MP:0000219	increased neutrophil cell number	Ache<em1(IMPC)Mbp>/Ache<+>	C57BL/6N-Ache<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408226	F	MP:0000689	abnormal spleen morphology	Adamts1<em1(IMPC)Mbp>/Adamts1<+>	C57BL/6N-Adamts1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408226	F	MP:0002989	small kidney	Adamts1<em1(IMPC)Mbp>/Adamts1<+>	C57BL/6N-Adamts1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408226	F	MP:0002135	abnormal kidney morphology	Adamts1<em1(IMPC)Mbp>/Adamts1<+>	C57BL/6N-Adamts1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408226	M	MP:0002188	small heart	Adamts1<em1(IMPC)Mbp>/Adamts1<+>	C57BL/6N-Adamts1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408226	F	MP:0002092	abnormal eye morphology	Adamts1<em1(IMPC)Mbp>/Adamts1<+>	C57BL/6N-Adamts1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408226	F	MP:0000691	enlarged spleen	Adamts1<em1(IMPC)Mbp>/Adamts1<+>	C57BL/6N-Adamts1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408226	M	MP:0000266	abnormal heart morphology	Adamts1<em1(IMPC)Mbp>/Adamts1<+>	C57BL/6N-Adamts1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408227	M	MP:0001614	abnormal blood vessel morphology	Adamts1<em1(IMPC)Mbp>/Adamts1<em1(IMPC)Mbp>	C57BL/6N-Adamts1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408228	F	MP:0003795	abnormal bone structure	Adamts4<tm1b(EUCOMM)Hmgu>/Adamts4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adamts4<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408228	F	MP:0010052	increased grip strength	Adamts4<tm1b(EUCOMM)Hmgu>/Adamts4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adamts4<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408229	M	MP:0001402	decreased locomotor activity	Adora2a<em1(IMPC)H>/Adora2a<em1(IMPC)H>	C57BL/6N-Adora2a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408229	F	MP:0005559	increased circulating glucose level	Adora2a<em1(IMPC)H>/Adora2a<em1(IMPC)H>	C57BL/6N-Adora2a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408229	M	MP:0002941	increased circulating alanine transaminase level	Adora2a<em1(IMPC)H>/Adora2a<em1(IMPC)H>	C57BL/6N-Adora2a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408229	F	MP:0000219	increased neutrophil cell number	Adora2a<em1(IMPC)H>/Adora2a<em1(IMPC)H>	C57BL/6N-Adora2a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408229	M	MP:0005343	increased circulating aspartate transaminase level	Adora2a<em1(IMPC)H>/Adora2a<em1(IMPC)H>	C57BL/6N-Adora2a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408229	F	MP:0010024	increased total body fat amount	Adora2a<em1(IMPC)H>/Adora2a<em1(IMPC)H>	C57BL/6N-Adora2a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408229	F	MP:0005016	decreased lymphocyte cell number	Adora2a<em1(IMPC)H>/Adora2a<em1(IMPC)H>	C57BL/6N-Adora2a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408229	M	MP:0020421	increased freezing behavior	Adora2a<em1(IMPC)H>/Adora2a<em1(IMPC)H>	C57BL/6N-Adora2a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408229	F	MP:0002874	decreased hemoglobin content	Adora2a<em1(IMPC)H>/Adora2a<em1(IMPC)H>	C57BL/6N-Adora2a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408230	M	MP:0000280	thin ventricular wall	Adtrp<em1(IMPC)Bay>/Adtrp<em1(IMPC)Bay>	C57BL/6N-Adtrp<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408231	F	MP:0004953	decreased spleen weight	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	F	MP:0001120	abnormal uterus morphology	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	M	MP:0000538	abnormal urinary bladder morphology	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	F	MP:0009142	decreased prepulse inhibition	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	M	MP:0000598	abnormal liver morphology	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	F	MP:0000266	abnormal heart morphology	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	M	MP:0011625	cystolithiasis	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	M	MP:0002060	abnormal skin morphology	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	M	MP:0002339	abnormal lymph node morphology	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	F	MP:0000692	small spleen	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	F	MP:0002188	small heart	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	M	MP:0002135	abnormal kidney morphology	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	M	MP:0000599	enlarged liver	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	M	MP:0000494	abnormal cecum morphology	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	M	MP:0000702	enlarged lymph nodes	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	M	MP:0003068	enlarged kidney	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408231	M	MP:0005084	abnormal gallbladder morphology	Afdn<em1(IMPC)Mbp>/Afdn<+>	C57BL/6N-Afdn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408234	F	MP:0001297	microphthalmia	Aloxe3<em1(IMPC)Mbp>/Aloxe3<em1(IMPC)Mbp>	C57BL/6N-Aloxe3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408235	F	MP:0000841	abnormal hindbrain morphology	Ambra1<em1(IMPC)Bay>/Ambra1<em1(IMPC)Bay>	C57BL/6N-Ambra1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408235	M	MP:0008797	facial cleft	Ambra1<em1(IMPC)Bay>/Ambra1<em1(IMPC)Bay>	C57BL/6N-Ambra1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408235	F	MP:0003720	abnormal neural tube closure	Ambra1<em1(IMPC)Bay>/Ambra1<em1(IMPC)Bay>	C57BL/6N-Ambra1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408235	F	MP:0000897	abnormal midbrain morphology	Ambra1<em1(IMPC)Bay>/Ambra1<em1(IMPC)Bay>	C57BL/6N-Ambra1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408235	M	MP:0003054	spina bifida	Ambra1<em1(IMPC)Bay>/Ambra1<em1(IMPC)Bay>	C57BL/6N-Ambra1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408235	F	MP:0000438	abnormal cranium morphology	Ambra1<em1(IMPC)Bay>/Ambra1<em1(IMPC)Bay>	C57BL/6N-Ambra1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408236	F	MP:0013279	increased fasting circulating glucose level	Angptl3<tm2b(KOMP)Wtsi>/Angptl3<tm2b(KOMP)Wtsi>	C57BL/6N-Angptl3<tm2b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408236	F	MP:0009709	hydrometra	Angptl3<tm2b(KOMP)Wtsi>/Angptl3<tm2b(KOMP)Wtsi>	C57BL/6N-Angptl3<tm2b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408236	F	MP:0000702	enlarged lymph nodes	Angptl3<tm2b(KOMP)Wtsi>/Angptl3<tm2b(KOMP)Wtsi>	C57BL/6N-Angptl3<tm2b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408236	M	MP:0002644	decreased circulating triglyceride level	Angptl3<tm2b(KOMP)Wtsi>/Angptl3<tm2b(KOMP)Wtsi>	C57BL/6N-Angptl3<tm2b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408236	F	MP:0004906	enlarged uterus	Angptl3<tm2b(KOMP)Wtsi>/Angptl3<tm2b(KOMP)Wtsi>	C57BL/6N-Angptl3<tm2b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408239	F	MP:0008935	decreased mean platelet volume	Aopep<tm1b(KOMP)Wtsi>/Aopep<tm1b(KOMP)Wtsi>	C57BL/6N-Aopep<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408239	M	MP:0000538	abnormal urinary bladder morphology	Aopep<tm1b(KOMP)Wtsi>/Aopep<tm1b(KOMP)Wtsi>	C57BL/6N-Aopep<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408239	F	MP:0002968	increased circulating alkaline phosphatase level	Aopep<tm1b(KOMP)Wtsi>/Aopep<tm1b(KOMP)Wtsi>	C57BL/6N-Aopep<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408240	M	MP:0006243	impaired pupillary reflex	Ap1s2<em1(IMPC)Mbp>/Y	C57BL/6N-Ap1s2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408242	F	MP:0001392	abnormal locomotor behavior	Ap3b2<em1(IMPC)H>/Ap3b2<em1(IMPC)H>	C57BL/6N-Ap3b2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408242	F	MP:0000745	tremors	Ap3b2<em1(IMPC)H>/Ap3b2<em1(IMPC)H>	C57BL/6N-Ap3b2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408243	F	MP:0003020	decreased circulating chloride level	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408243	F	MP:0002311	abnormal inspiratory capacity	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408243	M	MP:0004599	abnormal vertebral arch morphology	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408243	M	MP:0000137	abnormal vertebrae morphology	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408243	F	MP:0001399	hyperactivity	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408243	M	MP:0001146	abnormal testis morphology	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408243	F	MP:0001364	decreased anxiety-related response	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408243	F	MP:0005278	abnormal cholesterol homeostasis	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408243	M	MP:0001147	small testis	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408243	M	MP:0013279	increased fasting circulating glucose level	Ap4e1<tm1b(KOMP)Wtsi>/Ap4e1<tm1b(KOMP)Wtsi>	C57BL/6N-Ap4e1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408244	F	MP:0005567	decreased circulating total protein level	Arhgap42<em1(IMPC)H>/Arhgap42<em1(IMPC)H>	C57BL/6NTac-Arhgap42<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408246	M	MP:0001925	male infertility	Odad2<em1(IMPC)Mbp>/Odad2<em1(IMPC)Mbp>	C57BL/6N-Odad2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408246	M	MP:0000692	small spleen	Odad2<em1(IMPC)Mbp>/Odad2<em1(IMPC)Mbp>	C57BL/6N-Odad2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408248	F	MP:0000277	abnormal heart shape	Asb16<em1(IMPC)Ccpcz>/Asb16<em1(IMPC)Ccpcz>	C57BL/6N-Asb16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408248	F	MP:0000703	abnormal thymus morphology	Asb16<em1(IMPC)Ccpcz>/Asb16<em1(IMPC)Ccpcz>	C57BL/6N-Asb16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408248	F	MP:0000266	abnormal heart morphology	Asb16<em1(IMPC)Ccpcz>/Asb16<em1(IMPC)Ccpcz>	C57BL/6N-Asb16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408248	F	MP:0000709	enlarged thymus	Asb16<em1(IMPC)Ccpcz>/Asb16<em1(IMPC)Ccpcz>	C57BL/6N-Asb16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408249	M	MP:0001146	abnormal testis morphology	Asb4<em1(IMPC)Ccpcz>/Asb4<em1(IMPC)Ccpcz>	C57BL/6N-Asb4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408249	F	MP:0000367	abnormal coat/ hair morphology	Asb4<em1(IMPC)Ccpcz>/Asb4<em1(IMPC)Ccpcz>	C57BL/6N-Asb4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408249	M	MP:0002631	abnormal epididymis morphology	Asb4<em1(IMPC)Ccpcz>/Asb4<em1(IMPC)Ccpcz>	C57BL/6N-Asb4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408250	F	MP:0000709	enlarged thymus	Asb5<em1(IMPC)Ccpcz>/Asb5<em1(IMPC)Ccpcz>	C57BL/6N-Asb5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408250	F	MP:0000703	abnormal thymus morphology	Asb5<em1(IMPC)Ccpcz>/Asb5<em1(IMPC)Ccpcz>	C57BL/6N-Asb5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408250	M	MP:0005634	decreased circulating sodium level	Asb5<em1(IMPC)Ccpcz>/Asb5<em1(IMPC)Ccpcz>	C57BL/6N-Asb5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408251	M	MP:0005565	increased blood urea nitrogen level	Atf2<tm1b(EUCOMM)Hmgu>/Atf2<+>	C57BL/6N-Atf2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408251	F	MP:0002060	abnormal skin morphology	Atf2<tm1b(EUCOMM)Hmgu>/Atf2<+>	C57BL/6N-Atf2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408251	F	MP:0008935	decreased mean platelet volume	Atf2<tm1b(EUCOMM)Hmgu>/Atf2<+>	C57BL/6N-Atf2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408251	M	MP:0001262	decreased body weight	Atf2<tm1b(EUCOMM)Hmgu>/Atf2<+>	C57BL/6N-Atf2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408251	M	MP:0001146	abnormal testis morphology	Atf2<tm1b(EUCOMM)Hmgu>/Atf2<+>	C57BL/6N-Atf2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408251	M	MP:0001147	small testis	Atf2<tm1b(EUCOMM)Hmgu>/Atf2<+>	C57BL/6N-Atf2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408251	M	MP:0000538	abnormal urinary bladder morphology	Atf2<tm1b(EUCOMM)Hmgu>/Atf2<+>	C57BL/6N-Atf2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408251	M	MP:0002135	abnormal kidney morphology	Atf2<tm1b(EUCOMM)Hmgu>/Atf2<+>	C57BL/6N-Atf2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408251	F	MP:0003020	decreased circulating chloride level	Atf2<tm1b(EUCOMM)Hmgu>/Atf2<+>	C57BL/6N-Atf2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408251	F	MP:0011044	increased lung elastance	Atf2<tm1b(EUCOMM)Hmgu>/Atf2<+>	C57BL/6N-Atf2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408251	M	MP:0013279	increased fasting circulating glucose level	Atf2<tm1b(EUCOMM)Hmgu>/Atf2<+>	C57BL/6N-Atf2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408251	M	MP:0000266	abnormal heart morphology	Atf2<tm1b(EUCOMM)Hmgu>/Atf2<+>	C57BL/6N-Atf2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408251	M	MP:0000274	enlarged heart	Atf2<tm1b(EUCOMM)Hmgu>/Atf2<+>	C57BL/6N-Atf2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408252	M	MP:0003961	decreased lean body mass	Atg4b<tm1b(EUCOMM)Hmgu>/Atg4b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atg4b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408252	F	MP:0009142	decreased prepulse inhibition	Atg4b<tm1b(EUCOMM)Hmgu>/Atg4b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atg4b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408252	F	MP:0001304	cataract	Atg4b<tm1b(EUCOMM)Hmgu>/Atg4b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atg4b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408252	F	MP:0001513	limb grasping	Atg4b<tm1b(EUCOMM)Hmgu>/Atg4b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atg4b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408252	M	MP:0002100	abnormal tooth morphology	Atg4b<tm1b(EUCOMM)Hmgu>/Atg4b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atg4b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408252	F	MP:0002764	short tibia	Atg4b<tm1b(EUCOMM)Hmgu>/Atg4b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atg4b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408252	F	MP:0002941	increased circulating alanine transaminase level	Atg4b<tm1b(EUCOMM)Hmgu>/Atg4b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atg4b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408252	M	MP:0005179	decreased circulating cholesterol level	Atg4b<tm1b(EUCOMM)Hmgu>/Atg4b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atg4b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408252	M	MP:0000186	decreased circulating HDL cholesterol level	Atg4b<tm1b(EUCOMM)Hmgu>/Atg4b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atg4b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408252	F	MP:0005419	decreased circulating serum albumin level	Atg4b<tm1b(EUCOMM)Hmgu>/Atg4b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Atg4b<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408253	F	MP:0000266	abnormal heart morphology	Bbs1<em1(IMPC)Mbp>/Bbs1<+>	C57BL/6N-Bbs1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408253	F	MP:0001293	anophthalmia	Bbs1<em1(IMPC)Mbp>/Bbs1<+>	C57BL/6N-Bbs1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408253	F	MP:0002188	small heart	Bbs1<em1(IMPC)Mbp>/Bbs1<+>	C57BL/6N-Bbs1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408253	F	MP:0002092	abnormal eye morphology	Bbs1<em1(IMPC)Mbp>/Bbs1<+>	C57BL/6N-Bbs1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408255	F	MP:0011110	preweaning lethality, incomplete penetrance	Bcl9l<em1(IMPC)Bay>/Bcl9l<em1(IMPC)Bay>	C57BL/6N-Bcl9l<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408256	F	MP:0005016	decreased lymphocyte cell number	Bean1<em1(IMPC)H>/Bean1<em1(IMPC)H>	C57BL/6N-Bean1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408256	F	MP:0005011	increased eosinophil cell number	Bean1<em1(IMPC)H>/Bean1<em1(IMPC)H>	C57BL/6N-Bean1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408256	M	MP:0001406	abnormal gait	Bean1<em1(IMPC)H>/Bean1<em1(IMPC)H>	C57BL/6N-Bean1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408257	F	MP:0001700	abnormal embryo turning	Bicc1<em1(IMPC)Mbp>/Bicc1<em1(IMPC)Mbp>	C57BL/6N-Bicc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408257	F	MP:0000269	abnormal heart looping	Bicc1<em1(IMPC)Mbp>/Bicc1<em1(IMPC)Mbp>	C57BL/6N-Bicc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408257	M	MP:0011100	preweaning lethality, complete penetrance	Bicc1<em1(IMPC)Mbp>/Bicc1<em1(IMPC)Mbp>	C57BL/6N-Bicc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408257	F	MP:0001785	edema	Bicc1<em1(IMPC)Mbp>/Bicc1<em1(IMPC)Mbp>	C57BL/6N-Bicc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408258	M	MP:0000689	abnormal spleen morphology	Bloc1s6<em1(IMPC)Mbp>/Bloc1s6<em1(IMPC)Mbp>	C57BL/6N-Bloc1s6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408258	M	MP:0000691	enlarged spleen	Bloc1s6<em1(IMPC)Mbp>/Bloc1s6<em1(IMPC)Mbp>	C57BL/6N-Bloc1s6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408258	F	MP:0002965	increased circulating serum albumin level	Bloc1s6<em1(IMPC)Mbp>/Bloc1s6<em1(IMPC)Mbp>	C57BL/6N-Bloc1s6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408258	F	MP:0002339	abnormal lymph node morphology	Bloc1s6<em1(IMPC)Mbp>/Bloc1s6<em1(IMPC)Mbp>	C57BL/6N-Bloc1s6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408258	M	MP:0000274	enlarged heart	Bloc1s6<em1(IMPC)Mbp>/Bloc1s6<em1(IMPC)Mbp>	C57BL/6N-Bloc1s6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408258	M	MP:0000266	abnormal heart morphology	Bloc1s6<em1(IMPC)Mbp>/Bloc1s6<em1(IMPC)Mbp>	C57BL/6N-Bloc1s6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408259	M	MP:0002079	increased circulating insulin level	Bnip3<em1(IMPC)Mbp>/Bnip3<em1(IMPC)Mbp>	C57BL/6N-Bnip3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408259	M	MP:0005178	increased circulating cholesterol level	Bnip3<em1(IMPC)Mbp>/Bnip3<em1(IMPC)Mbp>	C57BL/6N-Bnip3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408259	M	MP:0005293	impaired glucose tolerance	Bnip3<em1(IMPC)Mbp>/Bnip3<em1(IMPC)Mbp>	C57BL/6N-Bnip3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408259	F	MP:0001333	absent optic nerve	Bnip3<em1(IMPC)Mbp>/Bnip3<em1(IMPC)Mbp>	C57BL/6N-Bnip3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408260	F	MP:0013520	increased CD4-positive NK T cell number	Btbd1<tm1a(KOMP)Wtsi>/Btbd1<tm1a(KOMP)Wtsi>	C57BL/6N-Btbd1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408260	F	MP:0003604	single kidney	Btbd1<tm1a(KOMP)Wtsi>/Btbd1<tm1a(KOMP)Wtsi>	C57BL/6N-Btbd1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408260	F	MP:0002135	abnormal kidney morphology	Btbd1<tm1a(KOMP)Wtsi>/Btbd1<tm1a(KOMP)Wtsi>	C57BL/6N-Btbd1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408260	F	MP:0005567	decreased circulating total protein level	Btbd1<tm1a(KOMP)Wtsi>/Btbd1<tm1a(KOMP)Wtsi>	C57BL/6N-Btbd1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408261	F	MP:0002339	abnormal lymph node morphology	Btbd2<em1(IMPC)Mbp>/Btbd2<em1(IMPC)Mbp>	C57BL/6N-Btbd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408261	M	MP:0000601	small liver	Btbd2<em1(IMPC)Mbp>/Btbd2<em1(IMPC)Mbp>	C57BL/6N-Btbd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408261	F	MP:0000194	increased circulating calcium level	Btbd2<em1(IMPC)Mbp>/Btbd2<em1(IMPC)Mbp>	C57BL/6N-Btbd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408261	F	MP:0000702	enlarged lymph nodes	Btbd2<em1(IMPC)Mbp>/Btbd2<em1(IMPC)Mbp>	C57BL/6N-Btbd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408261	M	MP:0001488	increased startle reflex	Btbd2<em1(IMPC)Mbp>/Btbd2<em1(IMPC)Mbp>	C57BL/6N-Btbd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408261	M	MP:0000598	abnormal liver morphology	Btbd2<em1(IMPC)Mbp>/Btbd2<em1(IMPC)Mbp>	C57BL/6N-Btbd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408261	M	MP:0002590	increased mean corpuscular volume	Btbd2<em1(IMPC)Mbp>/Btbd2<em1(IMPC)Mbp>	C57BL/6N-Btbd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408262	F	MP:0000137	abnormal vertebrae morphology	Btbd3<tm1b(EUCOMM)Hmgu>/Btbd3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Btbd3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408262	M	MP:0013890	increased CD8-positive, CD25-positive alpha-beta T cell number	Btbd3<tm1b(EUCOMM)Hmgu>/Btbd3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Btbd3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408263	F	MP:0000702	enlarged lymph nodes	Btc<em1(IMPC)Mbp>/Btc<em1(IMPC)Mbp>	C57BL/6N-Btc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408263	F	MP:0002339	abnormal lymph node morphology	Btc<em1(IMPC)Mbp>/Btc<em1(IMPC)Mbp>	C57BL/6N-Btc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408263	M	MP:0000219	increased neutrophil cell number	Btc<em1(IMPC)Mbp>/Btc<em1(IMPC)Mbp>	C57BL/6N-Btc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408264	F	MP:0001926	female infertility	C1ql2<em1(IMPC)Mbp>/C1ql2<em1(IMPC)Mbp>	C57BL/6N-C1ql2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408264	M	MP:0003068	enlarged kidney	C1ql2<em1(IMPC)Mbp>/C1ql2<em1(IMPC)Mbp>	C57BL/6N-C1ql2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408264	F	MP:0000689	abnormal spleen morphology	C1ql2<em1(IMPC)Mbp>/C1ql2<em1(IMPC)Mbp>	C57BL/6N-C1ql2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408264	M	MP:0002135	abnormal kidney morphology	C1ql2<em1(IMPC)Mbp>/C1ql2<em1(IMPC)Mbp>	C57BL/6N-C1ql2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408265	M	MP:0001697	abnormal embryo size	C2cd3<em1(IMPC)Tcp>/C2cd3<em1(IMPC)Tcp>	C57BL/6N-C2cd3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408265	M	MP:0003984	embryonic growth retardation	C2cd3<em1(IMPC)Tcp>/C2cd3<em1(IMPC)Tcp>	C57BL/6N-C2cd3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408266	F	MP:0002941	increased circulating alanine transaminase level	Cabcoco1<tm1a(KOMP)Wtsi>/Cabcoco1<tm1a(KOMP)Wtsi>	C57BL/6N-Cabcoco1<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6408266	F	MP:0005343	increased circulating aspartate transaminase level	Cabcoco1<tm1a(KOMP)Wtsi>/Cabcoco1<tm1a(KOMP)Wtsi>	C57BL/6N-Cabcoco1<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6408266	F	MP:0001120	abnormal uterus morphology	Cabcoco1<tm1a(KOMP)Wtsi>/Cabcoco1<tm1a(KOMP)Wtsi>	C57BL/6N-Cabcoco1<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6408266	M	MP:0000266	abnormal heart morphology	Cabcoco1<tm1a(KOMP)Wtsi>/Cabcoco1<tm1a(KOMP)Wtsi>	C57BL/6N-Cabcoco1<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6408266	M	MP:0000274	enlarged heart	Cabcoco1<tm1a(KOMP)Wtsi>/Cabcoco1<tm1a(KOMP)Wtsi>	C57BL/6N-Cabcoco1<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6408266	F	MP:0009709	hydrometra	Cabcoco1<tm1a(KOMP)Wtsi>/Cabcoco1<tm1a(KOMP)Wtsi>	C57BL/6N-Cabcoco1<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6408266	M	MP:0001925	male infertility	Cabcoco1<tm1a(KOMP)Wtsi>/Cabcoco1<tm1a(KOMP)Wtsi>	C57BL/6N-Cabcoco1<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6408267	M	MP:0002100	abnormal tooth morphology	Cabp5<tm1b(KOMP)Wtsi>/Cabp5<tm1b(KOMP)Wtsi>	C57BL/6N-Cabp5<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408267	M	MP:0005293	impaired glucose tolerance	Cabp5<tm1b(KOMP)Wtsi>/Cabp5<tm1b(KOMP)Wtsi>	C57BL/6N-Cabp5<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408269	M	MP:0001402	decreased locomotor activity	Cacna2d1<em1(IMPC)Mbp>/Cacna2d1<em1(IMPC)Mbp>	C57BL/6N-Cacna2d1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408269	M	MP:0000689	abnormal spleen morphology	Cacna2d1<em1(IMPC)Mbp>/Cacna2d1<em1(IMPC)Mbp>	C57BL/6N-Cacna2d1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408269	M	MP:0000692	small spleen	Cacna2d1<em1(IMPC)Mbp>/Cacna2d1<em1(IMPC)Mbp>	C57BL/6N-Cacna2d1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408269	F	MP:0001417	decreased exploration in new environment	Cacna2d1<em1(IMPC)Mbp>/Cacna2d1<em1(IMPC)Mbp>	C57BL/6N-Cacna2d1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408269	F	MP:0000220	increased monocyte cell number	Cacna2d1<em1(IMPC)Mbp>/Cacna2d1<em1(IMPC)Mbp>	C57BL/6N-Cacna2d1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408269	F	MP:0010124	decreased bone mineral content	Cacna2d1<em1(IMPC)Mbp>/Cacna2d1<em1(IMPC)Mbp>	C57BL/6N-Cacna2d1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408269	F	MP:0020420	abnormal freezing behavior	Cacna2d1<em1(IMPC)Mbp>/Cacna2d1<em1(IMPC)Mbp>	C57BL/6N-Cacna2d1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408270	F	MP:0009142	decreased prepulse inhibition	Cad<em1(IMPC)Mbp>/Cad<+>	C57BL/6N-Cad<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408272	F	MP:0005278	abnormal cholesterol homeostasis	Capn10<tm1b(EUCOMM)Wtsi>/Capn10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Capn10<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6408272	F	MP:0001399	hyperactivity	Capn10<tm1b(EUCOMM)Wtsi>/Capn10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Capn10<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6408272	F	MP:0005344	increased circulating bilirubin level	Capn10<tm1b(EUCOMM)Wtsi>/Capn10<tm1b(EUCOMM)Wtsi>	C57BL/6N-Capn10<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6408273	F	MP:0011960	abnormal eye anterior chamber depth	Cbarp<tm2e.1(EUCOMM)Hmgu>/Cbarp<tm2e.1(EUCOMM)Hmgu>	C57BL/6N-Cbarp<tm2e.1(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408273	F	MP:0001399	hyperactivity	Cbarp<tm2e.1(EUCOMM)Hmgu>/Cbarp<tm2e.1(EUCOMM)Hmgu>	C57BL/6N-Cbarp<tm2e.1(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408273	F	MP:0001363	increased anxiety-related response	Cbarp<tm2e.1(EUCOMM)Hmgu>/Cbarp<tm2e.1(EUCOMM)Hmgu>	C57BL/6N-Cbarp<tm2e.1(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408273	F	MP:0001258	decreased body length	Cbarp<tm2e.1(EUCOMM)Hmgu>/Cbarp<tm2e.1(EUCOMM)Hmgu>	C57BL/6N-Cbarp<tm2e.1(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408273	F	MP:0001417	decreased exploration in new environment	Cbarp<tm2e.1(EUCOMM)Hmgu>/Cbarp<tm2e.1(EUCOMM)Hmgu>	C57BL/6N-Cbarp<tm2e.1(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408273	F	MP:0001402	decreased locomotor activity	Cbarp<tm2e.1(EUCOMM)Hmgu>/Cbarp<tm2e.1(EUCOMM)Hmgu>	C57BL/6N-Cbarp<tm2e.1(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408274	M	MP:0002757	decreased vertical activity	Cbr3<em1(IMPC)Ics>/Cbr3<em1(IMPC)Ics>	C57BL/6N-Cbr3<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408274	M	MP:0004924	abnormal behavior	Cbr3<em1(IMPC)Ics>/Cbr3<em1(IMPC)Ics>	C57BL/6N-Cbr3<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408274	M	MP:0001364	decreased anxiety-related response	Cbr3<em1(IMPC)Ics>/Cbr3<em1(IMPC)Ics>	C57BL/6N-Cbr3<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408274	M	MP:0020870	decreased thigmotaxis	Cbr3<em1(IMPC)Ics>/Cbr3<em1(IMPC)Ics>	C57BL/6N-Cbr3<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408274	M	MP:0001417	decreased exploration in new environment	Cbr3<em1(IMPC)Ics>/Cbr3<em1(IMPC)Ics>	C57BL/6N-Cbr3<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408276	M	MP:0003231	abnormal placenta vasculature	Ccdc25<em1(IMPC)Mbp>/Ccdc25<em1(IMPC)Mbp>	C57BL/6N-Ccdc25<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408276	M	MP:0011110	preweaning lethality, incomplete penetrance	Ccdc25<em1(IMPC)Mbp>/Ccdc25<em1(IMPC)Mbp>	C57BL/6N-Ccdc25<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408276	M	MP:0001711	abnormal placenta morphology	Ccdc25<em1(IMPC)Mbp>/Ccdc25<em1(IMPC)Mbp>	C57BL/6N-Ccdc25<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408279	M	MP:0000572	abnormal autopod morphology	Cckbr<em1(IMPC)H>/Cckbr<em1(IMPC)H>	C57BL/6N-Cckbr<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408282	M	MP:0003131	increased erythrocyte cell number	Cdc20b<em1(IMPC)Wtsi>/Cdc20b<em1(IMPC)Wtsi>	C57BL/6N-Cdc20b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408282	M	MP:0001552	increased circulating triglyceride level	Cdc20b<em1(IMPC)Wtsi>/Cdc20b<em1(IMPC)Wtsi>	C57BL/6N-Cdc20b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408282	M	MP:0002608	increased hematocrit	Cdc20b<em1(IMPC)Wtsi>/Cdc20b<em1(IMPC)Wtsi>	C57BL/6N-Cdc20b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408283	F	MP:0010024	increased total body fat amount	Cdc27<tm1dIcs>/Cdc27<+>	C57BL/6N-Cdc27<tm1dIcs>/Ics	N	MGI:5576271
MGI:6408283	F	MP:0001417	decreased exploration in new environment	Cdc27<tm1dIcs>/Cdc27<+>	C57BL/6N-Cdc27<tm1dIcs>/Ics	N	MGI:5576271
MGI:6408283	F	MP:0003961	decreased lean body mass	Cdc27<tm1dIcs>/Cdc27<+>	C57BL/6N-Cdc27<tm1dIcs>/Ics	N	MGI:5576271
MGI:6408285	F	MP:0000692	small spleen	Cdcp2<em1(IMPC)Mbp>/Cdcp2<em1(IMPC)Mbp>	C57BL/6N-Cdcp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408285	F	MP:0009084	blind uterus	Cdcp2<em1(IMPC)Mbp>/Cdcp2<em1(IMPC)Mbp>	C57BL/6N-Cdcp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408287	F	MP:0001297	microphthalmia	Cds1<em1(IMPC)Mbp>/Cds1<em1(IMPC)Mbp>	C57BL/6N-Cds1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408287	M	MP:0001925	male infertility	Cds1<em1(IMPC)Mbp>/Cds1<em1(IMPC)Mbp>	C57BL/6N-Cds1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408287	F	MP:0002092	abnormal eye morphology	Cds1<em1(IMPC)Mbp>/Cds1<em1(IMPC)Mbp>	C57BL/6N-Cds1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408288	F	MP:0002875	decreased erythrocyte cell number	Cdyl2<em1(IMPC)Tcp>/Cdyl2<em1(IMPC)Tcp>	C57BL/6N-Cdyl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408288	M	MP:0020421	increased freezing behavior	Cdyl2<em1(IMPC)Tcp>/Cdyl2<em1(IMPC)Tcp>	C57BL/6N-Cdyl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408289	F	MP:0001697	abnormal embryo size	Celf1<em1(IMPC)Bay>/Celf1<em1(IMPC)Bay>	C57BL/6N-Celf1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408291	M	MP:0001614	abnormal blood vessel morphology	Cep290<em1(IMPC)Mbp>/Cep290<em1(IMPC)Mbp>	C57BL/6N-Cep290<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408297	M	MP:0005178	increased circulating cholesterol level	Cidec<tm1b(EUCOMM)Wtsi>/Cidec<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cidec<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6408297	M	MP:0002590	increased mean corpuscular volume	Cidec<tm1b(EUCOMM)Wtsi>/Cidec<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cidec<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6408297	F	MP:0002966	decreased circulating alkaline phosphatase level	Cidec<tm1b(EUCOMM)Wtsi>/Cidec<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cidec<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6408298	M	MP:0010025	decreased total body fat amount	Clcnka<tm1b(EUCOMM)Hmgu>/Clcnka<tm1b(EUCOMM)Hmgu>	C57BL/6N-Clcnka<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408298	F	MP:0003019	increased circulating chloride level	Clcnka<tm1b(EUCOMM)Hmgu>/Clcnka<tm1b(EUCOMM)Hmgu>	C57BL/6N-Clcnka<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408299	M	MP:0002968	increased circulating alkaline phosphatase level	Cldn3<em1(IMPC)H>/Cldn3<em1(IMPC)H>	C57BL/6N-Cldn3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408299	F	MP:0001529	abnormal vocalization	Cldn3<em1(IMPC)H>/Cldn3<em1(IMPC)H>	C57BL/6N-Cldn3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408300	M	MP:0001510	abnormal coat appearance	Cluh<em1(IMPC)Ccpcz>/Cluh<+>	C57BL/6N-Cluh<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408300	M	MP:0002997	enlarged seminal vesicle	Cluh<em1(IMPC)Ccpcz>/Cluh<+>	C57BL/6N-Cluh<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408300	M	MP:0008259	abnormal optic disk morphology	Cluh<em1(IMPC)Ccpcz>/Cluh<+>	C57BL/6N-Cluh<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408300	F	MP:0013676	increased Ly6C-positive mature NK cell number	Cluh<em1(IMPC)Ccpcz>/Cluh<+>	C57BL/6N-Cluh<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408300	M	MP:0002059	abnormal seminal vesicle morphology	Cluh<em1(IMPC)Ccpcz>/Cluh<+>	C57BL/6N-Cluh<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408300	M	MP:0002060	abnormal skin morphology	Cluh<em1(IMPC)Ccpcz>/Cluh<+>	C57BL/6N-Cluh<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408303	F	MP:0000702	enlarged lymph nodes	Cntn5<em1(IMPC)Mbp>/Cntn5<em1(IMPC)Mbp>	C57BL/6N-Cntn5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408303	M	MP:0002941	increased circulating alanine transaminase level	Cntn5<em1(IMPC)Mbp>/Cntn5<em1(IMPC)Mbp>	C57BL/6N-Cntn5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408303	F	MP:0002339	abnormal lymph node morphology	Cntn5<em1(IMPC)Mbp>/Cntn5<em1(IMPC)Mbp>	C57BL/6N-Cntn5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408304	M	MP:0002059	abnormal seminal vesicle morphology	Coa6<em1(IMPC)Ccpcz>/Coa6<+>	C57BL/6N-Coa6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408304	M	MP:0002135	abnormal kidney morphology	Coa6<em1(IMPC)Ccpcz>/Coa6<+>	C57BL/6N-Coa6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408304	M	MP:0003917	increased kidney weight	Coa6<em1(IMPC)Ccpcz>/Coa6<+>	C57BL/6N-Coa6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408305	M	MP:0000063	decreased bone mineral density	Cog4<em1(IMPC)Bay>/Cog4<+>	C57BL/6N-Cog4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408305	F	MP:0010123	increased bone mineral content	Cog4<em1(IMPC)Bay>/Cog4<+>	C57BL/6N-Cog4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408308	M	MP:0012362	increased large unstained cell number	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408308	F	MP:0002968	increased circulating alkaline phosphatase level	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408308	M	MP:0000218	increased leukocyte cell number	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408308	M	MP:0008935	decreased mean platelet volume	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408308	M	MP:0005016	decreased lymphocyte cell number	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408308	M	MP:0000274	enlarged heart	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408308	M	MP:0000219	increased neutrophil cell number	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408308	M	MP:0000691	enlarged spleen	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408308	M	MP:0008259	abnormal optic disk morphology	Col1a2<tm1b(EUCOMM)Wtsi>/Col1a2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Col1a2<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408309	F	MP:0003984	embryonic growth retardation	Col27a1<em1(IMPC)Mbp>/Col27a1<em1(IMPC)Mbp>	C57BL/6N-Col27a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408309	M	MP:0001614	abnormal blood vessel morphology	Col27a1<em1(IMPC)Mbp>/Col27a1<em1(IMPC)Mbp>	C57BL/6N-Col27a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408309	F	MP:0003743	abnormal facial morphology	Col27a1<em1(IMPC)Mbp>/Col27a1<em1(IMPC)Mbp>	C57BL/6N-Col27a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408309	M	MP:0001914	hemorrhage	Col27a1<em1(IMPC)Mbp>/Col27a1<em1(IMPC)Mbp>	C57BL/6N-Col27a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408310	F	MP:0010053	decreased grip strength	Col6a3<em1(IMPC)Tcp>/Col6a3<em1(IMPC)Tcp>	C57BL/6N-Col6a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408310	M	MP:0001258	decreased body length	Col6a3<em1(IMPC)Tcp>/Col6a3<em1(IMPC)Tcp>	C57BL/6N-Col6a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408310	M	MP:0000702	enlarged lymph nodes	Col6a3<em1(IMPC)Tcp>/Col6a3<em1(IMPC)Tcp>	C57BL/6N-Col6a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408310	F	MP:0003233	prolonged QT interval	Col6a3<em1(IMPC)Tcp>/Col6a3<em1(IMPC)Tcp>	C57BL/6N-Col6a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408310	M	MP:0003068	enlarged kidney	Col6a3<em1(IMPC)Tcp>/Col6a3<em1(IMPC)Tcp>	C57BL/6N-Col6a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408310	M	MP:0011874	enlarged urinary bladder	Col6a3<em1(IMPC)Tcp>/Col6a3<em1(IMPC)Tcp>	C57BL/6N-Col6a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408311	F	MP:0001258	decreased body length	Col9a3<em1(IMPC)Tcp>/Col9a3<em1(IMPC)Tcp>	C57BL/6N-Col9a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408311	M	MP:0002059	abnormal seminal vesicle morphology	Col9a3<em1(IMPC)Tcp>/Col9a3<em1(IMPC)Tcp>	C57BL/6N-Col9a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408311	F	MP:0000691	enlarged spleen	Col9a3<em1(IMPC)Tcp>/Col9a3<em1(IMPC)Tcp>	C57BL/6N-Col9a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408311	M	MP:0000702	enlarged lymph nodes	Col9a3<em1(IMPC)Tcp>/Col9a3<em1(IMPC)Tcp>	C57BL/6N-Col9a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408311	M	MP:0001552	increased circulating triglyceride level	Col9a3<em1(IMPC)Tcp>/Col9a3<em1(IMPC)Tcp>	C57BL/6N-Col9a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408312	M	MP:0000692	small spleen	Colec12<em1(IMPC)Mbp>/Colec12<em1(IMPC)Mbp>	C57BL/6N-Colec12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408313	M	MP:0000111	cleft palate	Cramp1<em1(IMPC)Bay>/Cramp1<em1(IMPC)Bay>	C57BL/6N-Cramp1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408315	F	MP:0013278	decreased fasting circulating glucose level	Cry1<em1(IMPC)H>/Cry1<em1(IMPC)H>	C57BL/6N-Cry1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408317	M	MP:0001146	abnormal testis morphology	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	F	MP:0004924	abnormal behavior	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	M	MP:0002644	decreased circulating triglyceride level	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	M	MP:0001925	male infertility	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	M	MP:0000186	decreased circulating HDL cholesterol level	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	F	MP:0001364	decreased anxiety-related response	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	M	MP:0001147	small testis	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	F	MP:0002574	increased vertical activity	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	M	MP:0002060	abnormal skin morphology	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	M	MP:0000274	enlarged heart	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	M	MP:0005344	increased circulating bilirubin level	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	M	MP:0002188	small heart	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	M	MP:0005560	decreased circulating glucose level	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	F	MP:0020870	decreased thigmotaxis	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408317	M	MP:0000266	abnormal heart morphology	Csnk2a2<em1(IMPC)Mbp>/Csnk2a2<em1(IMPC)Mbp>	C57BL/6N-Csnk2a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408319	F	MP:0001785	edema	Ctbp2<em1(IMPC)Bay>/Ctbp2<em1(IMPC)Bay>	C57BL/6N-Ctbp2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408319	F	MP:0000288	abnormal pericardium morphology	Ctbp2<em1(IMPC)Bay>/Ctbp2<em1(IMPC)Bay>	C57BL/6N-Ctbp2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408319	F	MP:0001700	abnormal embryo turning	Ctbp2<em1(IMPC)Bay>/Ctbp2<em1(IMPC)Bay>	C57BL/6N-Ctbp2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408319	F	MP:0000266	abnormal heart morphology	Ctbp2<em1(IMPC)Bay>/Ctbp2<em1(IMPC)Bay>	C57BL/6N-Ctbp2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408319	F	MP:0001691	abnormal somite shape	Ctbp2<em1(IMPC)Bay>/Ctbp2<em1(IMPC)Bay>	C57BL/6N-Ctbp2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408320	F	MP:0009476	enlarged cecum	Ctrc<tm1b(EUCOMM)Hmgu>/Ctrc<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ctrc<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408320	M	MP:0000559	abnormal femur morphology	Ctrc<tm1b(EUCOMM)Hmgu>/Ctrc<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ctrc<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408322	M	MP:0003020	decreased circulating chloride level	Cul4a<tm1b(EUCOMM)Hmgu>/Cul4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cul4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408322	M	MP:0005627	increased circulating potassium level	Cul4a<tm1b(EUCOMM)Hmgu>/Cul4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cul4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408322	M	MP:0001925	male infertility	Cul4a<tm1b(EUCOMM)Hmgu>/Cul4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cul4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408322	F	MP:0009455	enhanced cued conditioning behavior	Cul4a<tm1b(EUCOMM)Hmgu>/Cul4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cul4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408322	M	MP:0001146	abnormal testis morphology	Cul4a<tm1b(EUCOMM)Hmgu>/Cul4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cul4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408322	M	MP:0008935	decreased mean platelet volume	Cul4a<tm1b(EUCOMM)Hmgu>/Cul4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cul4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408322	M	MP:0001147	small testis	Cul4a<tm1b(EUCOMM)Hmgu>/Cul4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cul4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408322	M	MP:0001417	decreased exploration in new environment	Cul4a<tm1b(EUCOMM)Hmgu>/Cul4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cul4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408322	M	MP:0013279	increased fasting circulating glucose level	Cul4a<tm1b(EUCOMM)Hmgu>/Cul4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cul4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408323	M	MP:0003984	embryonic growth retardation	Cxadr<em1(IMPC)Mbp>/Cxadr<em1(IMPC)Mbp>	C57BL/6N-Cxadr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408323	M	MP:0000266	abnormal heart morphology	Cxadr<em1(IMPC)Mbp>/Cxadr<em1(IMPC)Mbp>	C57BL/6N-Cxadr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408324	F	MP:0000220	increased monocyte cell number	Cxcl1<em1(IMPC)Mbp>/Cxcl1<em1(IMPC)Mbp>	C57BL/6N-Cxcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408324	M	MP:0002339	abnormal lymph node morphology	Cxcl1<em1(IMPC)Mbp>/Cxcl1<em1(IMPC)Mbp>	C57BL/6N-Cxcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408324	F	MP:0000063	decreased bone mineral density	Cxcl1<em1(IMPC)Mbp>/Cxcl1<em1(IMPC)Mbp>	C57BL/6N-Cxcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408324	M	MP:0000702	enlarged lymph nodes	Cxcl1<em1(IMPC)Mbp>/Cxcl1<em1(IMPC)Mbp>	C57BL/6N-Cxcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408324	F	MP:0010124	decreased bone mineral content	Cxcl1<em1(IMPC)Mbp>/Cxcl1<em1(IMPC)Mbp>	C57BL/6N-Cxcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408324	F	MP:0002092	abnormal eye morphology	Cxcl1<em1(IMPC)Mbp>/Cxcl1<em1(IMPC)Mbp>	C57BL/6N-Cxcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408326	M	MP:0008259	abnormal optic disk morphology	Dbnl<tm1b(KOMP)Wtsi>/Dbnl<tm1b(KOMP)Wtsi>	C57BL/6N-Dbnl<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408326	M	MP:0005567	decreased circulating total protein level	Dbnl<tm1b(KOMP)Wtsi>/Dbnl<tm1b(KOMP)Wtsi>	C57BL/6N-Dbnl<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408326	M	MP:0005419	decreased circulating serum albumin level	Dbnl<tm1b(KOMP)Wtsi>/Dbnl<tm1b(KOMP)Wtsi>	C57BL/6N-Dbnl<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408326	M	MP:0011941	increased fluid intake	Dbnl<tm1b(KOMP)Wtsi>/Dbnl<tm1b(KOMP)Wtsi>	C57BL/6N-Dbnl<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408326	F	MP:0001402	decreased locomotor activity	Dbnl<tm1b(KOMP)Wtsi>/Dbnl<tm1b(KOMP)Wtsi>	C57BL/6N-Dbnl<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408326	F	MP:0011965	decreased total retina thickness	Dbnl<tm1b(KOMP)Wtsi>/Dbnl<tm1b(KOMP)Wtsi>	C57BL/6N-Dbnl<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408326	M	MP:0000186	decreased circulating HDL cholesterol level	Dbnl<tm1b(KOMP)Wtsi>/Dbnl<tm1b(KOMP)Wtsi>	C57BL/6N-Dbnl<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408326	F	MP:0010052	increased grip strength	Dbnl<tm1b(KOMP)Wtsi>/Dbnl<tm1b(KOMP)Wtsi>	C57BL/6N-Dbnl<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408326	F	MP:0002966	decreased circulating alkaline phosphatase level	Dbnl<tm1b(KOMP)Wtsi>/Dbnl<tm1b(KOMP)Wtsi>	C57BL/6N-Dbnl<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408326	M	MP:0002874	decreased hemoglobin content	Dbnl<tm1b(KOMP)Wtsi>/Dbnl<tm1b(KOMP)Wtsi>	C57BL/6N-Dbnl<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408326	M	MP:0005179	decreased circulating cholesterol level	Dbnl<tm1b(KOMP)Wtsi>/Dbnl<tm1b(KOMP)Wtsi>	C57BL/6N-Dbnl<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408326	F	MP:0002833	increased heart weight	Dbnl<tm1b(KOMP)Wtsi>/Dbnl<tm1b(KOMP)Wtsi>	C57BL/6N-Dbnl<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408326	F	MP:0001488	increased startle reflex	Dbnl<tm1b(KOMP)Wtsi>/Dbnl<tm1b(KOMP)Wtsi>	C57BL/6N-Dbnl<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408327	M	MP:0005016	decreased lymphocyte cell number	Dcaf12<em1(IMPC)Ccpcz>/Dcaf12<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408327	M	MP:0000219	increased neutrophil cell number	Dcaf12<em1(IMPC)Ccpcz>/Dcaf12<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408327	M	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number	Dcaf12<em1(IMPC)Ccpcz>/Dcaf12<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408327	F	MP:0001417	decreased exploration in new environment	Dcaf12<em1(IMPC)Ccpcz>/Dcaf12<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408327	F	MP:0005655	increased aggression	Dcaf12<em1(IMPC)Ccpcz>/Dcaf12<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408327	M	MP:0013772	increased effector memory T-helper cell number	Dcaf12<em1(IMPC)Ccpcz>/Dcaf12<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408328	M	MP:0005627	increased circulating potassium level	Dcaf8<em1(IMPC)Ccpcz>/Dcaf8<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408328	F	MP:0011045	decreased lung elastance	Dcaf8<em1(IMPC)Ccpcz>/Dcaf8<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408328	M	MP:0000274	enlarged heart	Dcaf8<em1(IMPC)Ccpcz>/Dcaf8<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408328	F	MP:0000598	abnormal liver morphology	Dcaf8<em1(IMPC)Ccpcz>/Dcaf8<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408328	F	MP:0020421	increased freezing behavior	Dcaf8<em1(IMPC)Ccpcz>/Dcaf8<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408328	M	MP:0005565	increased blood urea nitrogen level	Dcaf8<em1(IMPC)Ccpcz>/Dcaf8<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408328	F	MP:0000689	abnormal spleen morphology	Dcaf8<em1(IMPC)Ccpcz>/Dcaf8<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408328	F	MP:0010895	increased lung compliance	Dcaf8<em1(IMPC)Ccpcz>/Dcaf8<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408328	F	MP:0000691	enlarged spleen	Dcaf8<em1(IMPC)Ccpcz>/Dcaf8<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408328	M	MP:0000266	abnormal heart morphology	Dcaf8<em1(IMPC)Ccpcz>/Dcaf8<em1(IMPC)Ccpcz>	C57BL/6N-Dcaf8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408330	M	MP:0002100	abnormal tooth morphology	Ddc<em1(IMPC)Hmgu>/Ddc<+>	C57BL/6N-Ddc<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408330	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Ddc<em1(IMPC)Hmgu>/Ddc<+>	C57BL/6N-Ddc<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408330	F	MP:0002590	increased mean corpuscular volume	Ddc<em1(IMPC)Hmgu>/Ddc<+>	C57BL/6N-Ddc<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408332	M	MP:0000538	abnormal urinary bladder morphology	Ddi2<tm1b(EUCOMM)Hmgu>/Ddi2<+>	C57BL/6N-Ddi2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408332	F	MP:0010935	increased airway resistance	Ddi2<tm1b(EUCOMM)Hmgu>/Ddi2<+>	C57BL/6N-Ddi2<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408334	M	MP:0002098	abnormal vibrissa morphology	Dele1<em2(IMPC)Ccpcz>/Dele1<em2(IMPC)Ccpcz>	C57BL/6N-Dele1<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408334	F	MP:0001126	abnormal ovary morphology	Dele1<em2(IMPC)Ccpcz>/Dele1<em2(IMPC)Ccpcz>	C57BL/6N-Dele1<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408334	F	MP:0004832	enlarged ovary	Dele1<em2(IMPC)Ccpcz>/Dele1<em2(IMPC)Ccpcz>	C57BL/6N-Dele1<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408335	M	MP:0000266	abnormal heart morphology	Dennd1a<em1(IMPC)Mbp>/Dennd1a<em1(IMPC)Mbp>	C57BL/6N-Dennd1a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408336	M	MP:0001258	decreased body length	Dgki<em1(IMPC)Wtsi>/Dgki<em1(IMPC)Wtsi>	C57BL/6N-Dgki<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408336	M	MP:0003443	increased circulating glycerol level	Dgki<em1(IMPC)Wtsi>/Dgki<em1(IMPC)Wtsi>	C57BL/6N-Dgki<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408336	M	MP:0003443	increased circulating glycerol level	Dgki<em1(IMPC)Wtsi>/Dgki<em1(IMPC)Wtsi>	C57BL/6N-Dgki<em1(IMPC)Wtsi>/Wtsi	N	32492392
MGI:6408337	M	MP:0002968	increased circulating alkaline phosphatase level	Dgkk<em1(IMPC)Ics>/Y	C57BL/6N-Dgkk<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408337	M	MP:0005178	increased circulating cholesterol level	Dgkk<em1(IMPC)Ics>/Y	C57BL/6N-Dgkk<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408337	M	MP:0001488	increased startle reflex	Dgkk<em1(IMPC)Ics>/Y	C57BL/6N-Dgkk<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408337	M	MP:0001556	increased circulating HDL cholesterol level	Dgkk<em1(IMPC)Ics>/Y	C57BL/6N-Dgkk<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408337	M	MP:0001392	abnormal locomotor behavior	Dgkk<em1(IMPC)Ics>/Y	C57BL/6N-Dgkk<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408337	M	MP:0010053	decreased grip strength	Dgkk<em1(IMPC)Ics>/Y	C57BL/6N-Dgkk<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408338	M	MP:0001614	abnormal blood vessel morphology	Dhcr7<em1(IMPC)Mbp>/Dhcr7<em1(IMPC)Mbp>	C57BL/6N-Dhcr7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408338	F	MP:0001297	microphthalmia	Dhcr7<em1(IMPC)Mbp>/Dhcr7<em1(IMPC)Mbp>	C57BL/6N-Dhcr7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408338	M	MP:0003984	embryonic growth retardation	Dhcr7<em1(IMPC)Mbp>/Dhcr7<em1(IMPC)Mbp>	C57BL/6N-Dhcr7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408339	F	MP:0002188	small heart	Dlx3<em1(IMPC)Mbp>/Dlx3<+>	C57BL/6N-Dlx3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408339	F	MP:0000266	abnormal heart morphology	Dlx3<em1(IMPC)Mbp>/Dlx3<+>	C57BL/6N-Dlx3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408339	F	MP:0002968	increased circulating alkaline phosphatase level	Dlx3<em1(IMPC)Mbp>/Dlx3<+>	C57BL/6N-Dlx3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408339	F	MP:0020421	increased freezing behavior	Dlx3<em1(IMPC)Mbp>/Dlx3<+>	C57BL/6N-Dlx3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408341	M	MP:0002339	abnormal lymph node morphology	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	C57BL/6N-Dnah2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408341	M	MP:0001925	male infertility	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	C57BL/6N-Dnah2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408341	M	MP:0001399	hyperactivity	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	C57BL/6N-Dnah2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408341	M	MP:0002059	abnormal seminal vesicle morphology	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	C57BL/6N-Dnah2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408342	M	MP:0002135	abnormal kidney morphology	Dnah6<em1(IMPC)Mbp>/Dnah6<em1(IMPC)Mbp>	C57BL/6N-Dnah6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408342	F	MP:0001120	abnormal uterus morphology	Dnah6<em1(IMPC)Mbp>/Dnah6<em1(IMPC)Mbp>	C57BL/6N-Dnah6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408342	F	MP:0009709	hydrometra	Dnah6<em1(IMPC)Mbp>/Dnah6<em1(IMPC)Mbp>	C57BL/6N-Dnah6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408342	M	MP:0000274	enlarged heart	Dnah6<em1(IMPC)Mbp>/Dnah6<em1(IMPC)Mbp>	C57BL/6N-Dnah6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408343	F	MP:0005343	increased circulating aspartate transaminase level	Dse<tm1b(EUCOMM)Hmgu>/Dse<+>	C57BL/6N-Dse<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408345	F	MP:0001700	abnormal embryo turning	Dsp<em1(IMPC)Mbp>/Dsp<em1(IMPC)Mbp>	C57BL/6N-Dsp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408345	F	MP:0000266	abnormal heart morphology	Dsp<em1(IMPC)Mbp>/Dsp<em1(IMPC)Mbp>	C57BL/6N-Dsp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408345	F	MP:0002884	abnormal pharyngeal arch morphology	Dsp<em1(IMPC)Mbp>/Dsp<em1(IMPC)Mbp>	C57BL/6N-Dsp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408345	F	MP:0003864	abnormal midbrain development	Dsp<em1(IMPC)Mbp>/Dsp<em1(IMPC)Mbp>	C57BL/6N-Dsp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408346	M	MP:0000274	enlarged heart	Dtx4<em1(IMPC)Ccpcz>/Dtx4<+>	C57BL/6N-Dtx4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408346	F	MP:0005293	impaired glucose tolerance	Dtx4<em1(IMPC)Ccpcz>/Dtx4<+>	C57BL/6N-Dtx4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408346	F	MP:0000709	enlarged thymus	Dtx4<em1(IMPC)Ccpcz>/Dtx4<+>	C57BL/6N-Dtx4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408346	M	MP:0010935	increased airway resistance	Dtx4<em1(IMPC)Ccpcz>/Dtx4<+>	C57BL/6N-Dtx4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408346	M	MP:0000266	abnormal heart morphology	Dtx4<em1(IMPC)Ccpcz>/Dtx4<+>	C57BL/6N-Dtx4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408346	F	MP:0000703	abnormal thymus morphology	Dtx4<em1(IMPC)Ccpcz>/Dtx4<+>	C57BL/6N-Dtx4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408346	F	MP:0002968	increased circulating alkaline phosphatase level	Dtx4<em1(IMPC)Ccpcz>/Dtx4<+>	C57BL/6N-Dtx4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408347	F	MP:0002339	abnormal lymph node morphology	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	F	MP:0001556	increased circulating HDL cholesterol level	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	F	MP:0000702	enlarged lymph nodes	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	M	MP:0002135	abnormal kidney morphology	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	M	MP:0002989	small kidney	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	F	MP:0013279	increased fasting circulating glucose level	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	M	MP:0010068	decreased red blood cell distribution width	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	M	MP:0005553	increased circulating creatinine level	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	F	MP:0005568	increased circulating total protein level	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	M	MP:0003402	decreased liver weight	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	M	MP:0000194	increased circulating calcium level	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	M	MP:0002590	increased mean corpuscular volume	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	F	MP:0001926	female infertility	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	M	MP:0000219	increased neutrophil cell number	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	M	MP:0002965	increased circulating serum albumin level	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	M	MP:0005016	decreased lymphocyte cell number	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408347	F	MP:0000691	enlarged spleen	Duox2<em1(IMPC)Mbp>/Duox2<em1(IMPC)Mbp>	C57BL/6N-Duox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408348	M	MP:0010025	decreased total body fat amount	Dus2<tm1b(EUCOMM)Wtsi>/Dus2<+>	C57BL/6N-Dus2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408348	M	MP:0010067	increased red blood cell distribution width	Dus2<tm1b(EUCOMM)Wtsi>/Dus2<+>	C57BL/6N-Dus2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408348	M	MP:0003960	increased lean body mass	Dus2<tm1b(EUCOMM)Wtsi>/Dus2<+>	C57BL/6N-Dus2<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408349	F	MP:0010053	decreased grip strength	Dusp3<tm1b(KOMP)Wtsi>/Dusp3<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Dusp3<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408349	M	MP:0010068	decreased red blood cell distribution width	Dusp3<tm1b(KOMP)Wtsi>/Dusp3<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Dusp3<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408349	M	MP:0010124	decreased bone mineral content	Dusp3<tm1b(KOMP)Wtsi>/Dusp3<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Dusp3<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408349	M	MP:0003443	increased circulating glycerol level	Dusp3<tm1b(KOMP)Wtsi>/Dusp3<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Dusp3<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408349	M	MP:0002079	increased circulating insulin level	Dusp3<tm1b(KOMP)Wtsi>/Dusp3<tm1b(KOMP)Wtsi>	B6Brd;B6Dnk;B6N-Tyr<c-Brd> Dusp3<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408350	M	MP:0011874	enlarged urinary bladder	Dym<em1(IMPC)Tcp>/Dym<em1(IMPC)Tcp>	C57BL/6N-Dym<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408350	M	MP:0002968	increased circulating alkaline phosphatase level	Dym<em1(IMPC)Tcp>/Dym<em1(IMPC)Tcp>	C57BL/6N-Dym<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408350	F	MP:0010052	increased grip strength	Dym<em1(IMPC)Tcp>/Dym<em1(IMPC)Tcp>	C57BL/6N-Dym<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408350	M	MP:0000186	decreased circulating HDL cholesterol level	Dym<em1(IMPC)Tcp>/Dym<em1(IMPC)Tcp>	C57BL/6N-Dym<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408350	M	MP:0001488	increased startle reflex	Dym<em1(IMPC)Tcp>/Dym<em1(IMPC)Tcp>	C57BL/6N-Dym<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408350	M	MP:0002941	increased circulating alanine transaminase level	Dym<em1(IMPC)Tcp>/Dym<em1(IMPC)Tcp>	C57BL/6N-Dym<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408350	M	MP:0002644	decreased circulating triglyceride level	Dym<em1(IMPC)Tcp>/Dym<em1(IMPC)Tcp>	C57BL/6N-Dym<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408350	M	MP:0005343	increased circulating aspartate transaminase level	Dym<em1(IMPC)Tcp>/Dym<em1(IMPC)Tcp>	C57BL/6N-Dym<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408350	F	MP:0010124	decreased bone mineral content	Dym<em1(IMPC)Tcp>/Dym<em1(IMPC)Tcp>	C57BL/6N-Dym<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408350	M	MP:0002590	increased mean corpuscular volume	Dym<em1(IMPC)Tcp>/Dym<em1(IMPC)Tcp>	C57BL/6N-Dym<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408350	M	MP:0002059	abnormal seminal vesicle morphology	Dym<em1(IMPC)Tcp>/Dym<em1(IMPC)Tcp>	C57BL/6N-Dym<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408350	F	MP:0003795	abnormal bone structure	Dym<em1(IMPC)Tcp>/Dym<em1(IMPC)Tcp>	C57BL/6N-Dym<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408350	M	MP:0005179	decreased circulating cholesterol level	Dym<em1(IMPC)Tcp>/Dym<em1(IMPC)Tcp>	C57BL/6N-Dym<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408351	F	MP:0005293	impaired glucose tolerance	Dync1h1<tm1dIcs>/Dync1h1<+>	C57BL/6N-Dync1h1<tm1dIcs>/Ics	N	MGI:5576271
MGI:6408351	M	MP:0001402	decreased locomotor activity	Dync1h1<tm1dIcs>/Dync1h1<+>	C57BL/6N-Dync1h1<tm1dIcs>/Ics	N	MGI:5576271
MGI:6408352	F	MP:0000692	small spleen	Ebf1<em1(IMPC)Mbp>/Ebf1<+>	C57BL/6N-Ebf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408352	M	MP:0000689	abnormal spleen morphology	Ebf1<em1(IMPC)Mbp>/Ebf1<+>	C57BL/6N-Ebf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408352	M	MP:0002339	abnormal lymph node morphology	Ebf1<em1(IMPC)Mbp>/Ebf1<+>	C57BL/6N-Ebf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408352	M	MP:0002965	increased circulating serum albumin level	Ebf1<em1(IMPC)Mbp>/Ebf1<+>	C57BL/6N-Ebf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408352	M	MP:0000702	enlarged lymph nodes	Ebf1<em1(IMPC)Mbp>/Ebf1<+>	C57BL/6N-Ebf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408352	F	MP:0002188	small heart	Ebf1<em1(IMPC)Mbp>/Ebf1<+>	C57BL/6N-Ebf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408352	F	MP:0002060	abnormal skin morphology	Ebf1<em1(IMPC)Mbp>/Ebf1<+>	C57BL/6N-Ebf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408352	M	MP:0000274	enlarged heart	Ebf1<em1(IMPC)Mbp>/Ebf1<+>	C57BL/6N-Ebf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408352	M	MP:0000691	enlarged spleen	Ebf1<em1(IMPC)Mbp>/Ebf1<+>	C57BL/6N-Ebf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408352	M	MP:0000598	abnormal liver morphology	Ebf1<em1(IMPC)Mbp>/Ebf1<+>	C57BL/6N-Ebf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408353	M	MP:0001711	abnormal placenta morphology	Ebf1<em1(IMPC)Mbp>/Ebf1<em1(IMPC)Mbp>	C57BL/6N-Ebf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408354	F	MP:0001926	female infertility	Ebf2<em1(IMPC)Mbp>/Ebf2<em1(IMPC)Mbp>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408354	F	MP:0011495	abnormal head shape	Ebf2<em1(IMPC)Mbp>/Ebf2<em1(IMPC)Mbp>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408354	F	MP:0003743	abnormal facial morphology	Ebf2<em1(IMPC)Mbp>/Ebf2<em1(IMPC)Mbp>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408355	F	MP:0003733	abnormal retina inner nuclear layer morphology	Efcab14<tm1b(KOMP)Wtsi>/Efcab14<tm1b(KOMP)Wtsi>	C57BL/6N-Efcab14<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408355	F	MP:0005333	decreased heart rate	Efcab14<tm1b(KOMP)Wtsi>/Efcab14<tm1b(KOMP)Wtsi>	C57BL/6N-Efcab14<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408355	F	MP:0002753	dilated heart left ventricle	Efcab14<tm1b(KOMP)Wtsi>/Efcab14<tm1b(KOMP)Wtsi>	C57BL/6N-Efcab14<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408360	M	MP:0001399	hyperactivity	Elavl4<em1(IMPC)H>/Elavl4<em1(IMPC)H>	C57BL/6NTac-Elavl4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408360	M	MP:0001406	abnormal gait	Elavl4<em1(IMPC)H>/Elavl4<em1(IMPC)H>	C57BL/6NTac-Elavl4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408360	M	MP:0001513	limb grasping	Elavl4<em1(IMPC)H>/Elavl4<em1(IMPC)H>	C57BL/6NTac-Elavl4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408360	F	MP:0010053	decreased grip strength	Elavl4<em1(IMPC)H>/Elavl4<em1(IMPC)H>	C57BL/6NTac-Elavl4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408361	F	MP:0002968	increased circulating alkaline phosphatase level	Elk3<em1(IMPC)Ics>/Elk3<+>	C57BL/6N-Elk3<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408361	M	MP:0001556	increased circulating HDL cholesterol level	Elk3<em1(IMPC)Ics>/Elk3<+>	C57BL/6N-Elk3<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408361	F	MP:0005178	increased circulating cholesterol level	Elk3<em1(IMPC)Ics>/Elk3<+>	C57BL/6N-Elk3<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408363	M	MP:0000692	small spleen	Ephb2<em1(IMPC)Mbp>/Ephb2<em1(IMPC)Mbp>	C57BL/6N-Ephb2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408364	M	MP:0002574	increased vertical activity	Erich3<em1(IMPC)Mbp>/Erich3<em1(IMPC)Mbp>	C57BL/6N-Erich3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408365	M	MP:0000702	enlarged lymph nodes	Erlin1<em1(IMPC)Tcp>/Erlin1<em1(IMPC)Tcp>	C57BL/6N-Erlin1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408365	M	MP:0000470	abnormal stomach morphology	Erlin1<em1(IMPC)Tcp>/Erlin1<em1(IMPC)Tcp>	C57BL/6N-Erlin1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408365	M	MP:0011874	enlarged urinary bladder	Erlin1<em1(IMPC)Tcp>/Erlin1<em1(IMPC)Tcp>	C57BL/6N-Erlin1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408365	M	MP:0000689	abnormal spleen morphology	Erlin1<em1(IMPC)Tcp>/Erlin1<em1(IMPC)Tcp>	C57BL/6N-Erlin1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408365	M	MP:0002941	increased circulating alanine transaminase level	Erlin1<em1(IMPC)Tcp>/Erlin1<em1(IMPC)Tcp>	C57BL/6N-Erlin1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408365	M	MP:0000598	abnormal liver morphology	Erlin1<em1(IMPC)Tcp>/Erlin1<em1(IMPC)Tcp>	C57BL/6N-Erlin1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408365	F	MP:0003961	decreased lean body mass	Erlin1<em1(IMPC)Tcp>/Erlin1<em1(IMPC)Tcp>	C57BL/6N-Erlin1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408365	F	MP:0001126	abnormal ovary morphology	Erlin1<em1(IMPC)Tcp>/Erlin1<em1(IMPC)Tcp>	C57BL/6N-Erlin1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408365	M	MP:0002768	small adrenal glands	Erlin1<em1(IMPC)Tcp>/Erlin1<em1(IMPC)Tcp>	C57BL/6N-Erlin1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408365	M	MP:0002092	abnormal eye morphology	Erlin1<em1(IMPC)Tcp>/Erlin1<em1(IMPC)Tcp>	C57BL/6N-Erlin1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408365	M	MP:0002059	abnormal seminal vesicle morphology	Erlin1<em1(IMPC)Tcp>/Erlin1<em1(IMPC)Tcp>	C57BL/6N-Erlin1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408365	F	MP:0000063	decreased bone mineral density	Erlin1<em1(IMPC)Tcp>/Erlin1<em1(IMPC)Tcp>	C57BL/6N-Erlin1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408366	M	MP:0002135	abnormal kidney morphology	Esrp1<em1(IMPC)Mbp>/Esrp1<+>	C57BL/6N-Esrp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408366	F	MP:0000063	decreased bone mineral density	Esrp1<em1(IMPC)Mbp>/Esrp1<+>	C57BL/6N-Esrp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408366	F	MP:0001126	abnormal ovary morphology	Esrp1<em1(IMPC)Mbp>/Esrp1<+>	C57BL/6N-Esrp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408366	M	MP:0003068	enlarged kidney	Esrp1<em1(IMPC)Mbp>/Esrp1<+>	C57BL/6N-Esrp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408366	M	MP:0002989	small kidney	Esrp1<em1(IMPC)Mbp>/Esrp1<+>	C57BL/6N-Esrp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408366	F	MP:0010124	decreased bone mineral content	Esrp1<em1(IMPC)Mbp>/Esrp1<+>	C57BL/6N-Esrp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408367	F	MP:0000562	polydactyly	Esrp1<em1(IMPC)Mbp>/Esrp1<em1(IMPC)Mbp>	C57BL/6N-Esrp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408367	F	MP:0002109	abnormal limb morphology	Esrp1<em1(IMPC)Mbp>/Esrp1<em1(IMPC)Mbp>	C57BL/6N-Esrp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408369	M	MP:0005553	increased circulating creatinine level	Fads6<tm1b(EUCOMM)Wtsi>/Fads6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fads6<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6408369	F	MP:0003271	abnormal duodenum morphology	Fads6<tm1b(EUCOMM)Wtsi>/Fads6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fads6<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6408369	F	MP:0000494	abnormal cecum morphology	Fads6<tm1b(EUCOMM)Wtsi>/Fads6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fads6<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6408369	M	MP:0002699	abnormal vitreous body morphology	Fads6<tm1b(EUCOMM)Wtsi>/Fads6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fads6<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6408369	M	MP:0000194	increased circulating calcium level	Fads6<tm1b(EUCOMM)Wtsi>/Fads6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fads6<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6408369	M	MP:0005565	increased blood urea nitrogen level	Fads6<tm1b(EUCOMM)Wtsi>/Fads6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fads6<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6408369	M	MP:0002060	abnormal skin morphology	Fads6<tm1b(EUCOMM)Wtsi>/Fads6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fads6<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6408369	M	MP:0005627	increased circulating potassium level	Fads6<tm1b(EUCOMM)Wtsi>/Fads6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fads6<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6408369	F	MP:0004906	enlarged uterus	Fads6<tm1b(EUCOMM)Wtsi>/Fads6<tm1b(EUCOMM)Wtsi>	C57BL/6N-Fads6<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6408370	F	MP:0001406	abnormal gait	Faf1<em1(IMPC)H>/Faf1<em1(IMPC)H>	C57BL/6NTac-Faf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408370	F	MP:0020421	increased freezing behavior	Faf1<em1(IMPC)H>/Faf1<em1(IMPC)H>	C57BL/6NTac-Faf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408370	M	MP:0001925	male infertility	Faf1<em1(IMPC)H>/Faf1<em1(IMPC)H>	C57BL/6NTac-Faf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408370	F	MP:0000745	tremors	Faf1<em1(IMPC)H>/Faf1<em1(IMPC)H>	C57BL/6NTac-Faf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408370	M	MP:0005560	decreased circulating glucose level	Faf1<em1(IMPC)H>/Faf1<em1(IMPC)H>	C57BL/6NTac-Faf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408370	F	MP:0008810	increased circulating iron level	Faf1<em1(IMPC)H>/Faf1<em1(IMPC)H>	C57BL/6NTac-Faf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408371	F	MP:0001289	persistence of hyaloid vascular system	Fam120b<tm1b(EUCOMM)Hmgu>/Fam120b<+>	C57BL/6N-Fam120b<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6408372	M	MP:0000219	increased neutrophil cell number	Hycc1<em1(IMPC)Ccpcz>/Hycc1<em1(IMPC)Ccpcz>	C57BL/6N-Hycc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408372	M	MP:0000618	small salivary gland	Hycc1<em1(IMPC)Ccpcz>/Hycc1<em1(IMPC)Ccpcz>	C57BL/6N-Hycc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408372	M	MP:0000220	increased monocyte cell number	Hycc1<em1(IMPC)Ccpcz>/Hycc1<em1(IMPC)Ccpcz>	C57BL/6N-Hycc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408372	M	MP:0010895	increased lung compliance	Hycc1<em1(IMPC)Ccpcz>/Hycc1<em1(IMPC)Ccpcz>	C57BL/6N-Hycc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408372	F	MP:0000709	enlarged thymus	Hycc1<em1(IMPC)Ccpcz>/Hycc1<em1(IMPC)Ccpcz>	C57BL/6N-Hycc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408372	M	MP:0011045	decreased lung elastance	Hycc1<em1(IMPC)Ccpcz>/Hycc1<em1(IMPC)Ccpcz>	C57BL/6N-Hycc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408372	F	MP:0005627	increased circulating potassium level	Hycc1<em1(IMPC)Ccpcz>/Hycc1<em1(IMPC)Ccpcz>	C57BL/6N-Hycc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408372	M	MP:0005344	increased circulating bilirubin level	Hycc1<em1(IMPC)Ccpcz>/Hycc1<em1(IMPC)Ccpcz>	C57BL/6N-Hycc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408372	M	MP:0002311	abnormal inspiratory capacity	Hycc1<em1(IMPC)Ccpcz>/Hycc1<em1(IMPC)Ccpcz>	C57BL/6N-Hycc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408372	F	MP:0011951	increased cardiac stroke volume	Hycc1<em1(IMPC)Ccpcz>/Hycc1<em1(IMPC)Ccpcz>	C57BL/6N-Hycc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408372	F	MP:0003394	increased cardiac output	Hycc1<em1(IMPC)Ccpcz>/Hycc1<em1(IMPC)Ccpcz>	C57BL/6N-Hycc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408372	F	MP:0005567	decreased circulating total protein level	Hycc1<em1(IMPC)Ccpcz>/Hycc1<em1(IMPC)Ccpcz>	C57BL/6N-Hycc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408372	M	MP:0000613	abnormal salivary gland morphology	Hycc1<em1(IMPC)Ccpcz>/Hycc1<em1(IMPC)Ccpcz>	C57BL/6N-Hycc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408373	F	MP:0010392	prolonged QRS complex duration	Nalf1<em1(IMPC)H>/Nalf1<+>	C57BL/6N-Nalf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408373	M	MP:0004357	long tibia	Nalf1<em1(IMPC)H>/Nalf1<+>	C57BL/6N-Nalf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408375	F	MP:0002188	small heart	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408375	F	MP:0000627	abnormal mammary gland morphology	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408375	M	MP:0004924	abnormal behavior	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408375	M	MP:0010053	decreased grip strength	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408375	M	MP:0001146	abnormal testis morphology	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408375	M	MP:0002135	abnormal kidney morphology	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408375	M	MP:0001402	decreased locomotor activity	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408375	F	MP:0000266	abnormal heart morphology	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408375	M	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408375	M	MP:0001147	small testis	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408375	M	MP:0001417	decreased exploration in new environment	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408375	M	MP:0005278	abnormal cholesterol homeostasis	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408375	F	MP:0000367	abnormal coat/ hair morphology	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408375	M	MP:0005627	increased circulating potassium level	Fam83h<em1(IMPC)Ccpcz>/Fam83h<em1(IMPC)Ccpcz>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408377	M	MP:0011874	enlarged urinary bladder	Fbxw10<em1(IMPC)Tcp>/Fbxw10<em1(IMPC)Tcp>	C57BL/6N-Fbxw10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408377	M	MP:0000702	enlarged lymph nodes	Fbxw10<em1(IMPC)Tcp>/Fbxw10<em1(IMPC)Tcp>	C57BL/6N-Fbxw10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408378	M	MP:0002599	increased mean platelet volume	Fer<em1(IMPC)Tcp>/Fer<+>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408378	M	MP:0002060	abnormal skin morphology	Fer<em1(IMPC)Tcp>/Fer<+>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408378	M	MP:0004952	increased spleen weight	Fer<em1(IMPC)Tcp>/Fer<+>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408378	F	MP:0000689	abnormal spleen morphology	Fer<em1(IMPC)Tcp>/Fer<+>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408378	M	MP:0010067	increased red blood cell distribution width	Fer<em1(IMPC)Tcp>/Fer<+>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408378	M	MP:0001417	decreased exploration in new environment	Fer<em1(IMPC)Tcp>/Fer<+>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408378	F	MP:0002989	small kidney	Fer<em1(IMPC)Tcp>/Fer<+>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408378	M	MP:0002059	abnormal seminal vesicle morphology	Fer<em1(IMPC)Tcp>/Fer<+>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408378	M	MP:0001325	abnormal retina morphology	Fer<em1(IMPC)Tcp>/Fer<+>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408379	M	MP:0000157	abnormal sternum morphology	Fer<em1(IMPC)Tcp>/Fer<em1(IMPC)Tcp>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408379	M	MP:0000691	enlarged spleen	Fer<em1(IMPC)Tcp>/Fer<em1(IMPC)Tcp>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408379	F	MP:0002092	abnormal eye morphology	Fer<em1(IMPC)Tcp>/Fer<em1(IMPC)Tcp>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408379	M	MP:0011110	preweaning lethality, incomplete penetrance	Fer<em1(IMPC)Tcp>/Fer<em1(IMPC)Tcp>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408379	M	MP:0000443	abnormal snout morphology	Fer<em1(IMPC)Tcp>/Fer<em1(IMPC)Tcp>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408379	F	MP:0002060	abnormal skin morphology	Fer<em1(IMPC)Tcp>/Fer<em1(IMPC)Tcp>	C57BL/6N-Fer<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408380	F	MP:0020870	decreased thigmotaxis	Fgf12<tm1b(KOMP)Wtsi>/Fgf12<tm1b(KOMP)Wtsi>	C57BL/6N-Fgf12<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408380	M	MP:0001510	abnormal coat appearance	Fgf12<tm1b(KOMP)Wtsi>/Fgf12<tm1b(KOMP)Wtsi>	C57BL/6N-Fgf12<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408381	F	MP:0010053	decreased grip strength	Fgf4<em1(IMPC)H>/Fgf4<+>	C57BL/6NTac-Fgf4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408383	M	MP:0000689	abnormal spleen morphology	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0002699	abnormal vitreous body morphology	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	F	MP:0001926	female infertility	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0004931	enlarged epididymis	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0005278	abnormal cholesterol homeostasis	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0001925	male infertility	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0009198	abnormal male genitalia morphology	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0010506	prolonged RR interval	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0001147	small testis	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0001304	cataract	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0002060	abnormal skin morphology	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0000702	enlarged lymph nodes	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0001157	small seminal vesicle	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0000692	small spleen	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0002591	decreased mean corpuscular volume	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0006415	absent testes	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0004930	small epididymis	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0005333	decreased heart rate	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0002339	abnormal lymph node morphology	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408383	M	MP:0000691	enlarged spleen	Fkbp4<em1(IMPC)Mbp>/Fkbp4<em1(IMPC)Mbp>	C57BL/6N-Fkbp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408384	F	MP:0005534	decreased body temperature	Flnc<em1(IMPC)Bay>/Flnc<+>	C57BL/6N-Flnc<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408385	F	MP:0001691	abnormal somite shape	Flnc<em1(IMPC)Bay>/Flnc<em1(IMPC)Bay>	C57BL/6N-Flnc<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408385	F	MP:0000266	abnormal heart morphology	Flnc<em1(IMPC)Bay>/Flnc<em1(IMPC)Bay>	C57BL/6N-Flnc<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408385	F	MP:0000269	abnormal heart looping	Flnc<em1(IMPC)Bay>/Flnc<em1(IMPC)Bay>	C57BL/6N-Flnc<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408386	F	MP:0010570	prolonged ST segment	Flywch2<tm4b(EUCOMM)Hmgu>/Flywch2<tm4b(EUCOMM)Hmgu>	C57BL/6N-Flywch2<tm4b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408387	F	MP:0000111	cleft palate	Focad<em1(IMPC)Bay>/Focad<em1(IMPC)Bay>	C57BL/6N-Focad<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408387	F	MP:0003743	abnormal facial morphology	Focad<em1(IMPC)Bay>/Focad<em1(IMPC)Bay>	C57BL/6N-Focad<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408387	F	MP:0001293	anophthalmia	Focad<em1(IMPC)Bay>/Focad<em1(IMPC)Bay>	C57BL/6N-Focad<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408388	M	MP:0001146	abnormal testis morphology	Foxe3<em1(IMPC)Mbp>/Foxe3<em1(IMPC)Mbp>	C57BL/6N-Foxe3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408388	M	MP:0001314	cornea opacity	Foxe3<em1(IMPC)Mbp>/Foxe3<em1(IMPC)Mbp>	C57BL/6N-Foxe3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408388	F	MP:0002060	abnormal skin morphology	Foxe3<em1(IMPC)Mbp>/Foxe3<em1(IMPC)Mbp>	C57BL/6N-Foxe3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408388	M	MP:0001293	anophthalmia	Foxe3<em1(IMPC)Mbp>/Foxe3<em1(IMPC)Mbp>	C57BL/6N-Foxe3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408388	M	MP:0001147	small testis	Foxe3<em1(IMPC)Mbp>/Foxe3<em1(IMPC)Mbp>	C57BL/6N-Foxe3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408390	M	MP:0003961	decreased lean body mass	Fut4<em1(IMPC)Ics>/Fut4<em1(IMPC)Ics>	C57BL/6N-Fut4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408390	M	MP:0010123	increased bone mineral content	Fut4<em1(IMPC)Ics>/Fut4<em1(IMPC)Ics>	C57BL/6N-Fut4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408390	F	MP:0005554	decreased circulating creatinine level	Fut4<em1(IMPC)Ics>/Fut4<em1(IMPC)Ics>	C57BL/6N-Fut4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408390	F	MP:0020420	abnormal freezing behavior	Fut4<em1(IMPC)Ics>/Fut4<em1(IMPC)Ics>	C57BL/6N-Fut4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408390	M	MP:0002135	abnormal kidney morphology	Fut4<em1(IMPC)Ics>/Fut4<em1(IMPC)Ics>	C57BL/6N-Fut4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408390	M	MP:0010024	increased total body fat amount	Fut4<em1(IMPC)Ics>/Fut4<em1(IMPC)Ics>	C57BL/6N-Fut4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408391	F	MP:0001914	hemorrhage	Fuz<em1(IMPC)Mbp>/Fuz<em1(IMPC)Mbp>	C57BL/6N-Fuz<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408391	F	MP:0008797	facial cleft	Fuz<em1(IMPC)Mbp>/Fuz<em1(IMPC)Mbp>	C57BL/6N-Fuz<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408391	F	MP:0002111	abnormal tail morphology	Fuz<em1(IMPC)Mbp>/Fuz<em1(IMPC)Mbp>	C57BL/6N-Fuz<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408393	M	MP:0002060	abnormal skin morphology	Fzd1<em1(IMPC)Mbp>/Fzd1<em1(IMPC)Mbp>	C57BL/6N-Fzd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408393	F	MP:0020420	abnormal freezing behavior	Fzd1<em1(IMPC)Mbp>/Fzd1<em1(IMPC)Mbp>	C57BL/6N-Fzd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408393	F	MP:0000218	increased leukocyte cell number	Fzd1<em1(IMPC)Mbp>/Fzd1<em1(IMPC)Mbp>	C57BL/6N-Fzd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408393	F	MP:0004924	abnormal behavior	Fzd1<em1(IMPC)Mbp>/Fzd1<em1(IMPC)Mbp>	C57BL/6N-Fzd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408393	M	MP:0005011	increased eosinophil cell number	Fzd1<em1(IMPC)Mbp>/Fzd1<em1(IMPC)Mbp>	C57BL/6N-Fzd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408393	F	MP:0000220	increased monocyte cell number	Fzd1<em1(IMPC)Mbp>/Fzd1<em1(IMPC)Mbp>	C57BL/6N-Fzd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408393	F	MP:0001364	decreased anxiety-related response	Fzd1<em1(IMPC)Mbp>/Fzd1<em1(IMPC)Mbp>	C57BL/6N-Fzd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408393	F	MP:0005013	increased lymphocyte cell number	Fzd1<em1(IMPC)Mbp>/Fzd1<em1(IMPC)Mbp>	C57BL/6N-Fzd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408394	M	MP:0010052	increased grip strength	Gabra2<em1(IMPC)H>/Gabra2<em1(IMPC)H>	C57BL/6N-Gabra2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408394	F	MP:0001314	cornea opacity	Gabra2<em1(IMPC)H>/Gabra2<em1(IMPC)H>	C57BL/6N-Gabra2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408394	F	MP:0001417	decreased exploration in new environment	Gabra2<em1(IMPC)H>/Gabra2<em1(IMPC)H>	C57BL/6N-Gabra2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408394	M	MP:0003960	increased lean body mass	Gabra2<em1(IMPC)H>/Gabra2<em1(IMPC)H>	C57BL/6N-Gabra2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408394	F	MP:0001512	trunk curl	Gabra2<em1(IMPC)H>/Gabra2<em1(IMPC)H>	C57BL/6N-Gabra2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408394	M	MP:0013278	decreased fasting circulating glucose level	Gabra2<em1(IMPC)H>/Gabra2<em1(IMPC)H>	C57BL/6N-Gabra2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408395	F	MP:0008806	increased circulating amylase level	Gba1<em1(IMPC)H>/Gba1<+>	C57BL/6N-Gba1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408395	F	MP:0010392	prolonged QRS complex duration	Gba1<em1(IMPC)H>/Gba1<+>	C57BL/6N-Gba1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408399	M	MP:0005178	increased circulating cholesterol level	Gemin4<em1(IMPC)Ics>/Gemin4<+>	C57BL/6N-Gemin4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408399	F	MP:0002968	increased circulating alkaline phosphatase level	Gemin4<em1(IMPC)Ics>/Gemin4<+>	C57BL/6N-Gemin4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408399	M	MP:0001556	increased circulating HDL cholesterol level	Gemin4<em1(IMPC)Ics>/Gemin4<+>	C57BL/6N-Gemin4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408399	F	MP:0005568	increased circulating total protein level	Gemin4<em1(IMPC)Ics>/Gemin4<+>	C57BL/6N-Gemin4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408399	M	MP:0010024	increased total body fat amount	Gemin4<em1(IMPC)Ics>/Gemin4<+>	C57BL/6N-Gemin4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408400	M	MP:0000266	abnormal heart morphology	Gin1<em1(IMPC)Mbp>/Gin1<em1(IMPC)Mbp>	C57BL/6N-Gin1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408400	M	MP:0000277	abnormal heart shape	Gin1<em1(IMPC)Mbp>/Gin1<em1(IMPC)Mbp>	C57BL/6N-Gin1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408400	F	MP:0000709	enlarged thymus	Gin1<em1(IMPC)Mbp>/Gin1<em1(IMPC)Mbp>	C57BL/6N-Gin1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408400	F	MP:0000703	abnormal thymus morphology	Gin1<em1(IMPC)Mbp>/Gin1<em1(IMPC)Mbp>	C57BL/6N-Gin1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408405	F	MP:0010088	decreased circulating fructosamine level	Gmip<tm1b(KOMP)Wtsi>/Gmip<tm1b(KOMP)Wtsi>	C57BL/6N-Gmip<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408406	M	MP:0003960	increased lean body mass	Gngt2<em1(IMPC)Bay>/Gngt2<em1(IMPC)Bay>	C57BL/6N-Gngt2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408406	F	MP:0011110	preweaning lethality, incomplete penetrance	Gngt2<em1(IMPC)Bay>/Gngt2<em1(IMPC)Bay>	C57BL/6N-Gngt2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408406	F	MP:0003731	abnormal retina outer nuclear layer morphology	Gngt2<em1(IMPC)Bay>/Gngt2<em1(IMPC)Bay>	C57BL/6N-Gngt2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408406	M	MP:0010025	decreased total body fat amount	Gngt2<em1(IMPC)Bay>/Gngt2<em1(IMPC)Bay>	C57BL/6N-Gngt2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408406	F	MP:0010579	increased heart left ventricle size	Gngt2<em1(IMPC)Bay>/Gngt2<em1(IMPC)Bay>	C57BL/6N-Gngt2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408406	F	MP:0013279	increased fasting circulating glucose level	Gngt2<em1(IMPC)Bay>/Gngt2<em1(IMPC)Bay>	C57BL/6N-Gngt2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408407	M	MP:0010024	increased total body fat amount	Gnl1<em1(IMPC)Tcp>/Gnl1<em1(IMPC)Tcp>	C57BL/6N-Gnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408407	M	MP:0001891	hydrocephaly	Gnl1<em1(IMPC)Tcp>/Gnl1<em1(IMPC)Tcp>	C57BL/6N-Gnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408407	F	MP:0001926	female infertility	Gnl1<em1(IMPC)Tcp>/Gnl1<em1(IMPC)Tcp>	C57BL/6N-Gnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408407	F	MP:0002599	increased mean platelet volume	Gnl1<em1(IMPC)Tcp>/Gnl1<em1(IMPC)Tcp>	C57BL/6N-Gnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408407	M	MP:0000438	abnormal cranium morphology	Gnl1<em1(IMPC)Tcp>/Gnl1<em1(IMPC)Tcp>	C57BL/6N-Gnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408407	F	MP:0002764	short tibia	Gnl1<em1(IMPC)Tcp>/Gnl1<em1(IMPC)Tcp>	C57BL/6N-Gnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408407	F	MP:0001513	limb grasping	Gnl1<em1(IMPC)Tcp>/Gnl1<em1(IMPC)Tcp>	C57BL/6N-Gnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408407	M	MP:0010511	shortened PR interval	Gnl1<em1(IMPC)Tcp>/Gnl1<em1(IMPC)Tcp>	C57BL/6N-Gnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408407	M	MP:0002574	increased vertical activity	Gnl1<em1(IMPC)Tcp>/Gnl1<em1(IMPC)Tcp>	C57BL/6N-Gnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408407	M	MP:0001925	male infertility	Gnl1<em1(IMPC)Tcp>/Gnl1<em1(IMPC)Tcp>	C57BL/6N-Gnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408407	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Gnl1<em1(IMPC)Tcp>/Gnl1<em1(IMPC)Tcp>	C57BL/6N-Gnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408407	F	MP:0010052	increased grip strength	Gnl1<em1(IMPC)Tcp>/Gnl1<em1(IMPC)Tcp>	C57BL/6N-Gnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408407	M	MP:0005293	impaired glucose tolerance	Gnl1<em1(IMPC)Tcp>/Gnl1<em1(IMPC)Tcp>	C57BL/6N-Gnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408409	M	MP:0002884	abnormal pharyngeal arch morphology	Got2<em1(IMPC)Mbp>/Got2<em1(IMPC)Mbp>	C57BL/6N-Got2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408410	F	MP:0001297	microphthalmia	Gp2<em1(IMPC)Mbp>/Gp2<em1(IMPC)Mbp>	C57BL/6N-Gp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408410	M	MP:0003179	thrombocytopenia	Gp2<em1(IMPC)Mbp>/Gp2<em1(IMPC)Mbp>	C57BL/6N-Gp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408410	M	MP:0002059	abnormal seminal vesicle morphology	Gp2<em1(IMPC)Mbp>/Gp2<em1(IMPC)Mbp>	C57BL/6N-Gp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408410	F	MP:0002092	abnormal eye morphology	Gp2<em1(IMPC)Mbp>/Gp2<em1(IMPC)Mbp>	C57BL/6N-Gp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408410	F	MP:0000639	abnormal adrenal gland morphology	Gp2<em1(IMPC)Mbp>/Gp2<em1(IMPC)Mbp>	C57BL/6N-Gp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408410	F	MP:0002060	abnormal skin morphology	Gp2<em1(IMPC)Mbp>/Gp2<em1(IMPC)Mbp>	C57BL/6N-Gp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408410	M	MP:0002997	enlarged seminal vesicle	Gp2<em1(IMPC)Mbp>/Gp2<em1(IMPC)Mbp>	C57BL/6N-Gp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408410	F	MP:0001293	anophthalmia	Gp2<em1(IMPC)Mbp>/Gp2<em1(IMPC)Mbp>	C57BL/6N-Gp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408410	F	MP:0002989	small kidney	Gp2<em1(IMPC)Mbp>/Gp2<em1(IMPC)Mbp>	C57BL/6N-Gp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408410	F	MP:0000266	abnormal heart morphology	Gp2<em1(IMPC)Mbp>/Gp2<em1(IMPC)Mbp>	C57BL/6N-Gp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408410	M	MP:0003642	absent seminal vesicle	Gp2<em1(IMPC)Mbp>/Gp2<em1(IMPC)Mbp>	C57BL/6N-Gp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408410	F	MP:0002188	small heart	Gp2<em1(IMPC)Mbp>/Gp2<em1(IMPC)Mbp>	C57BL/6N-Gp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408412	M	MP:0002764	short tibia	Gpr108<tm1b(EUCOMM)Hmgu>/Gpr108<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gpr108<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6408413	M	MP:0005505	thrombocytosis	Gpr146<em1(IMPC)H>/Gpr146<em1(IMPC)H>	C57BL/6NTac-Gpr146<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408413	F	MP:0004952	increased spleen weight	Gpr146<em1(IMPC)H>/Gpr146<em1(IMPC)H>	C57BL/6NTac-Gpr146<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408413	M	MP:0002941	increased circulating alanine transaminase level	Gpr146<em1(IMPC)H>/Gpr146<em1(IMPC)H>	C57BL/6NTac-Gpr146<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408413	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Gpr146<em1(IMPC)H>/Gpr146<em1(IMPC)H>	C57BL/6NTac-Gpr146<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408414	F	MP:0000432	abnormal head morphology	Gpr176<tm1b(EUCOMM)Hmgu>/Gpr176<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gpr176<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408414	F	MP:0005565	increased blood urea nitrogen level	Gpr176<tm1b(EUCOMM)Hmgu>/Gpr176<tm1b(EUCOMM)Hmgu>	C57BL/6N-Gpr176<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408415	M	MP:0020421	increased freezing behavior	Grhl2<em1(IMPC)Mbp>/Grhl2<+>	C57BL/6N-Grhl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408415	M	MP:0001488	increased startle reflex	Grhl2<em1(IMPC)Mbp>/Grhl2<+>	C57BL/6N-Grhl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408416	F	MP:0003232	abnormal forebrain development	Grhl2<em1(IMPC)Mbp>/Grhl2<em1(IMPC)Mbp>	C57BL/6N-Grhl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408417	F	MP:0008810	increased circulating iron level	Gria1<em1(IMPC)H>/Gria1<em1(IMPC)H>	C57BL/6N-Gria1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408417	F	MP:0009456	impaired cued conditioning behavior	Gria1<em1(IMPC)H>/Gria1<em1(IMPC)H>	C57BL/6N-Gria1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408417	M	MP:0001392	abnormal locomotor behavior	Gria1<em1(IMPC)H>/Gria1<em1(IMPC)H>	C57BL/6N-Gria1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408417	M	MP:0009142	decreased prepulse inhibition	Gria1<em1(IMPC)H>/Gria1<em1(IMPC)H>	C57BL/6N-Gria1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408418	M	MP:0010053	decreased grip strength	Gria2<em1(IMPC)H>/Gria2<+>	C57BL/6NTac-Gria2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408418	F	MP:0010392	prolonged QRS complex duration	Gria2<em1(IMPC)H>/Gria2<+>	C57BL/6NTac-Gria2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408418	M	MP:0002941	increased circulating alanine transaminase level	Gria2<em1(IMPC)H>/Gria2<+>	C57BL/6NTac-Gria2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408420	F	MP:0003960	increased lean body mass	Grik1<tm1b(KOMP)Mbp>/Grik1<tm1b(KOMP)Mbp>	C57BL/6N-Grik1<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6408420	F	MP:0010025	decreased total body fat amount	Grik1<tm1b(KOMP)Mbp>/Grik1<tm1b(KOMP)Mbp>	C57BL/6N-Grik1<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6408420	F	MP:0001399	hyperactivity	Grik1<tm1b(KOMP)Mbp>/Grik1<tm1b(KOMP)Mbp>	C57BL/6N-Grik1<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6408421	M	MP:0002092	abnormal eye morphology	Grik4<em1(IMPC)Mbp>/Grik4<em1(IMPC)Mbp>	C57BL/6N-Grik4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408421	F	MP:0003961	decreased lean body mass	Grik4<em1(IMPC)Mbp>/Grik4<em1(IMPC)Mbp>	C57BL/6N-Grik4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408421	F	MP:0010024	increased total body fat amount	Grik4<em1(IMPC)Mbp>/Grik4<em1(IMPC)Mbp>	C57BL/6N-Grik4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408421	F	MP:0005293	impaired glucose tolerance	Grik4<em1(IMPC)Mbp>/Grik4<em1(IMPC)Mbp>	C57BL/6N-Grik4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408422	M	MP:0002631	abnormal epididymis morphology	Grin3a<tm1b(EUCOMM)Hmgu>/Grin3a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Grin3a<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408423	F	MP:0000689	abnormal spleen morphology	Gsg1l<em1(IMPC)Mbp>/Gsg1l<em1(IMPC)Mbp>	C57BL/6N-Gsg1l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408423	M	MP:0010124	decreased bone mineral content	Gsg1l<em1(IMPC)Mbp>/Gsg1l<em1(IMPC)Mbp>	C57BL/6N-Gsg1l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408423	M	MP:0000702	enlarged lymph nodes	Gsg1l<em1(IMPC)Mbp>/Gsg1l<em1(IMPC)Mbp>	C57BL/6N-Gsg1l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408423	F	MP:0001293	anophthalmia	Gsg1l<em1(IMPC)Mbp>/Gsg1l<em1(IMPC)Mbp>	C57BL/6N-Gsg1l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408423	F	MP:0000691	enlarged spleen	Gsg1l<em1(IMPC)Mbp>/Gsg1l<em1(IMPC)Mbp>	C57BL/6N-Gsg1l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408423	F	MP:0010053	decreased grip strength	Gsg1l<em1(IMPC)Mbp>/Gsg1l<em1(IMPC)Mbp>	C57BL/6N-Gsg1l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408423	M	MP:0002339	abnormal lymph node morphology	Gsg1l<em1(IMPC)Mbp>/Gsg1l<em1(IMPC)Mbp>	C57BL/6N-Gsg1l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408423	M	MP:0000063	decreased bone mineral density	Gsg1l<em1(IMPC)Mbp>/Gsg1l<em1(IMPC)Mbp>	C57BL/6N-Gsg1l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408423	F	MP:0001126	abnormal ovary morphology	Gsg1l<em1(IMPC)Mbp>/Gsg1l<em1(IMPC)Mbp>	C57BL/6N-Gsg1l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408424	F	MP:0002968	increased circulating alkaline phosphatase level	Gstm5<em1(IMPC)Mbp>/Gstm5<em1(IMPC)Mbp>	C57BL/6N-Gstm5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408424	F	MP:0002965	increased circulating serum albumin level	Gstm5<em1(IMPC)Mbp>/Gstm5<em1(IMPC)Mbp>	C57BL/6N-Gstm5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408427	M	MP:0011874	enlarged urinary bladder	H2bc4<em1(IMPC)Tcp>/H2bc4<em1(IMPC)Tcp>	C57BL/6N-H2bc4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408427	F	MP:0002092	abnormal eye morphology	H2bc4<em1(IMPC)Tcp>/H2bc4<em1(IMPC)Tcp>	C57BL/6N-H2bc4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408427	F	MP:0002060	abnormal skin morphology	H2bc4<em1(IMPC)Tcp>/H2bc4<em1(IMPC)Tcp>	C57BL/6N-H2bc4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408427	F	MP:0000691	enlarged spleen	H2bc4<em1(IMPC)Tcp>/H2bc4<em1(IMPC)Tcp>	C57BL/6N-H2bc4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408428	M	MP:0013771	decreased effector memory T-helper cell number	Hcar1<em1(IMPC)Ccpcz>/Hcar1<em1(IMPC)Ccpcz>	C57BL/6N-Hcar1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408428	M	MP:0000558	abnormal tibia morphology	Hcar1<em1(IMPC)Ccpcz>/Hcar1<em1(IMPC)Ccpcz>	C57BL/6N-Hcar1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408428	M	MP:0002135	abnormal kidney morphology	Hcar1<em1(IMPC)Ccpcz>/Hcar1<em1(IMPC)Ccpcz>	C57BL/6N-Hcar1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408428	F	MP:0002968	increased circulating alkaline phosphatase level	Hcar1<em1(IMPC)Ccpcz>/Hcar1<em1(IMPC)Ccpcz>	C57BL/6N-Hcar1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408428	M	MP:0004509	abnormal pelvic girdle bone morphology	Hcar1<em1(IMPC)Ccpcz>/Hcar1<em1(IMPC)Ccpcz>	C57BL/6N-Hcar1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408429	M	MP:0000538	abnormal urinary bladder morphology	Hcar2<em1(IMPC)Ccpcz>/Hcar2<em1(IMPC)Ccpcz>	C57BL/6N-Hcar2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408433	F	MP:0001297	microphthalmia	Hmox1<em1(IMPC)Mbp>/Hmox1<+>	C57BL/6N-Hmox1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408434	M	MP:0011100	preweaning lethality, complete penetrance	Hmox1<em1(IMPC)Mbp>/Hmox1<em1(IMPC)Mbp>	C57BL/6N-Hmox1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408434	F	MP:0003984	embryonic growth retardation	Hmox1<em1(IMPC)Mbp>/Hmox1<em1(IMPC)Mbp>	C57BL/6N-Hmox1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408434	F	MP:0003743	abnormal facial morphology	Hmox1<em1(IMPC)Mbp>/Hmox1<em1(IMPC)Mbp>	C57BL/6N-Hmox1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408434	F	MP:0011495	abnormal head shape	Hmox1<em1(IMPC)Mbp>/Hmox1<em1(IMPC)Mbp>	C57BL/6N-Hmox1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408434	F	MP:0004258	abnormal placenta size	Hmox1<em1(IMPC)Mbp>/Hmox1<em1(IMPC)Mbp>	C57BL/6N-Hmox1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408434	F	MP:0001711	abnormal placenta morphology	Hmox1<em1(IMPC)Mbp>/Hmox1<em1(IMPC)Mbp>	C57BL/6N-Hmox1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408434	F	MP:0000428	abnormal craniofacial morphology	Hmox1<em1(IMPC)Mbp>/Hmox1<em1(IMPC)Mbp>	C57BL/6N-Hmox1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408435	F	MP:0002989	small kidney	Hnf4g<em1(IMPC)Mbp>/Hnf4g<em1(IMPC)Mbp>	C57BL/6N-Hnf4g<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408435	F	MP:0002135	abnormal kidney morphology	Hnf4g<em1(IMPC)Mbp>/Hnf4g<em1(IMPC)Mbp>	C57BL/6N-Hnf4g<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408436	F	MP:0010123	increased bone mineral content	Hpca<em1(IMPC)H>/Hpca<em1(IMPC)H>	C57BL/6NTac-Hpca<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408436	F	MP:0002968	increased circulating alkaline phosphatase level	Hpca<em1(IMPC)H>/Hpca<em1(IMPC)H>	C57BL/6NTac-Hpca<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408436	F	MP:0001392	abnormal locomotor behavior	Hpca<em1(IMPC)H>/Hpca<em1(IMPC)H>	C57BL/6NTac-Hpca<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408437	F	MP:0000157	abnormal sternum morphology	Hps6<em1(IMPC)Tcp>/Hps6<em1(IMPC)Tcp>	C57BL/6N-Hps6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408437	F	MP:0001258	decreased body length	Hps6<em1(IMPC)Tcp>/Hps6<em1(IMPC)Tcp>	C57BL/6N-Hps6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408437	M	MP:0000692	small spleen	Hps6<em1(IMPC)Tcp>/Hps6<em1(IMPC)Tcp>	C57BL/6N-Hps6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408437	M	MP:0000706	small thymus	Hps6<em1(IMPC)Tcp>/Hps6<em1(IMPC)Tcp>	C57BL/6N-Hps6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408437	F	MP:0002092	abnormal eye morphology	Hps6<em1(IMPC)Tcp>/Hps6<em1(IMPC)Tcp>	C57BL/6N-Hps6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408438	F	MP:0005343	increased circulating aspartate transaminase level	Hs3st3a1<tm1(KOMP)Vlcg>/Hs3st3a1<tm1(KOMP)Vlcg>	C57BL/6N-Hs3st3a1<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408438	F	MP:0005568	increased circulating total protein level	Hs3st3a1<tm1(KOMP)Vlcg>/Hs3st3a1<tm1(KOMP)Vlcg>	C57BL/6N-Hs3st3a1<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408438	M	MP:0003179	thrombocytopenia	Hs3st3a1<tm1(KOMP)Vlcg>/Hs3st3a1<tm1(KOMP)Vlcg>	C57BL/6N-Hs3st3a1<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408438	M	MP:0002833	increased heart weight	Hs3st3a1<tm1(KOMP)Vlcg>/Hs3st3a1<tm1(KOMP)Vlcg>	C57BL/6N-Hs3st3a1<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408438	M	MP:0002599	increased mean platelet volume	Hs3st3a1<tm1(KOMP)Vlcg>/Hs3st3a1<tm1(KOMP)Vlcg>	C57BL/6N-Hs3st3a1<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408438	M	MP:0010025	decreased total body fat amount	Hs3st3a1<tm1(KOMP)Vlcg>/Hs3st3a1<tm1(KOMP)Vlcg>	C57BL/6N-Hs3st3a1<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408438	F	MP:0002941	increased circulating alanine transaminase level	Hs3st3a1<tm1(KOMP)Vlcg>/Hs3st3a1<tm1(KOMP)Vlcg>	C57BL/6N-Hs3st3a1<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408439	M	MP:0001417	decreased exploration in new environment	Ifit1bl2<em1(IMPC)Bay>/Ifit1bl2<em1(IMPC)Bay>	C57BL/6N-Ifit1bl2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408439	M	MP:0010097	abnormal retina blood vessel morphology	Ifit1bl2<em1(IMPC)Bay>/Ifit1bl2<em1(IMPC)Bay>	C57BL/6N-Ifit1bl2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408441	M	MP:0002102	abnormal ear morphology	Ikzf2<em2(IMPC)H>/Ikzf2<em2(IMPC)H>	C57BL/6NTac-Ikzf2<em2(IMPC)H>/H	N	MGI:5576271
MGI:6408442	F	MP:0010052	increased grip strength	Il1r2<tm1a(EUCOMM)Wtsi>/Il1r2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Il1r2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408443	M	MP:0010067	increased red blood cell distribution width	Il6ra<em1(IMPC)Wtsi>/Il6ra<em1(IMPC)Wtsi>	C57BL/6N-Il6ra<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408444	F	MP:0002339	abnormal lymph node morphology	Inmt<em1(IMPC)Mbp>/Inmt<em1(IMPC)Mbp>	C57BL/6N-Inmt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408444	M	MP:0005292	improved glucose tolerance	Inmt<em1(IMPC)Mbp>/Inmt<em1(IMPC)Mbp>	C57BL/6N-Inmt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408444	F	MP:0000702	enlarged lymph nodes	Inmt<em1(IMPC)Mbp>/Inmt<em1(IMPC)Mbp>	C57BL/6N-Inmt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408448	M	MP:0003864	abnormal midbrain development	Ipo9<em1(IMPC)Bay>/Ipo9<em1(IMPC)Bay>	C57BL/6N-Ipo9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408448	M	MP:0003232	abnormal forebrain development	Ipo9<em1(IMPC)Bay>/Ipo9<em1(IMPC)Bay>	C57BL/6N-Ipo9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408448	M	MP:0006108	abnormal hindbrain development	Ipo9<em1(IMPC)Bay>/Ipo9<em1(IMPC)Bay>	C57BL/6N-Ipo9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408448	M	MP:0002861	abnormal tail bud morphology	Ipo9<em1(IMPC)Bay>/Ipo9<em1(IMPC)Bay>	C57BL/6N-Ipo9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408448	M	MP:0001785	edema	Ipo9<em1(IMPC)Bay>/Ipo9<em1(IMPC)Bay>	C57BL/6N-Ipo9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408448	M	MP:0000266	abnormal heart morphology	Ipo9<em1(IMPC)Bay>/Ipo9<em1(IMPC)Bay>	C57BL/6N-Ipo9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408448	M	MP:0001726	abnormal allantois morphology	Ipo9<em1(IMPC)Bay>/Ipo9<em1(IMPC)Bay>	C57BL/6N-Ipo9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408448	M	MP:0002884	abnormal pharyngeal arch morphology	Ipo9<em1(IMPC)Bay>/Ipo9<em1(IMPC)Bay>	C57BL/6N-Ipo9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408448	M	MP:0003720	abnormal neural tube closure	Ipo9<em1(IMPC)Bay>/Ipo9<em1(IMPC)Bay>	C57BL/6N-Ipo9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408448	M	MP:0002824	abnormal chorioallantoic fusion	Ipo9<em1(IMPC)Bay>/Ipo9<em1(IMPC)Bay>	C57BL/6N-Ipo9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408448	M	MP:0001672	abnormal embryo development	Ipo9<em1(IMPC)Bay>/Ipo9<em1(IMPC)Bay>	C57BL/6N-Ipo9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408449	F	MP:0000703	abnormal thymus morphology	Irf4<em1(IMPC)Mbp>/Irf4<em1(IMPC)Mbp>	C57BL/6N-Irf4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408449	F	MP:0001486	abnormal startle reflex	Irf4<em1(IMPC)Mbp>/Irf4<em1(IMPC)Mbp>	C57BL/6N-Irf4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408449	F	MP:0000709	enlarged thymus	Irf4<em1(IMPC)Mbp>/Irf4<em1(IMPC)Mbp>	C57BL/6N-Irf4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408451	F	MP:0005560	decreased circulating glucose level	Itga11<em1(IMPC)H>/Itga11<em1(IMPC)H>	C57BL/6N-Itga11<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408451	M	MP:0013278	decreased fasting circulating glucose level	Itga11<em1(IMPC)H>/Itga11<em1(IMPC)H>	C57BL/6N-Itga11<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408455	M	MP:0002059	abnormal seminal vesicle morphology	Jade2<em1(IMPC)Tcp>/Jade2<em1(IMPC)Tcp>	C57BL/6N-Jade2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408455	F	MP:0011874	enlarged urinary bladder	Jade2<em1(IMPC)Tcp>/Jade2<em1(IMPC)Tcp>	C57BL/6N-Jade2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408455	M	MP:0013278	decreased fasting circulating glucose level	Jade2<em1(IMPC)Tcp>/Jade2<em1(IMPC)Tcp>	C57BL/6N-Jade2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408455	M	MP:0009142	decreased prepulse inhibition	Jade2<em1(IMPC)Tcp>/Jade2<em1(IMPC)Tcp>	C57BL/6N-Jade2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408455	M	MP:0000157	abnormal sternum morphology	Jade2<em1(IMPC)Tcp>/Jade2<em1(IMPC)Tcp>	C57BL/6N-Jade2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408455	M	MP:0000692	small spleen	Jade2<em1(IMPC)Tcp>/Jade2<em1(IMPC)Tcp>	C57BL/6N-Jade2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408456	M	MP:0008806	increased circulating amylase level	Jmjd7<em1(IMPC)Wtsi>/Jmjd7<em1(IMPC)Wtsi>	C57BL/6N-Jmjd7<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408456	M	MP:0002079	increased circulating insulin level	Jmjd7<em1(IMPC)Wtsi>/Jmjd7<em1(IMPC)Wtsi>	C57BL/6N-Jmjd7<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408457	F	MP:0001293	anophthalmia	Jun<em1(IMPC)Mbp>/Jun<+>	C57BL/6N-Jun<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408457	F	MP:0000702	enlarged lymph nodes	Jun<em1(IMPC)Mbp>/Jun<+>	C57BL/6N-Jun<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408457	F	MP:0002339	abnormal lymph node morphology	Jun<em1(IMPC)Mbp>/Jun<+>	C57BL/6N-Jun<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408457	M	MP:0001399	hyperactivity	Jun<em1(IMPC)Mbp>/Jun<+>	C57BL/6N-Jun<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408458	F	MP:0003984	embryonic growth retardation	Jun<em1(IMPC)Mbp>/Jun<em1(IMPC)Mbp>	C57BL/6N-Jun<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408458	F	MP:0002151	abnormal neural tube morphology	Jun<em1(IMPC)Mbp>/Jun<em1(IMPC)Mbp>	C57BL/6N-Jun<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408460	F	MP:0000691	enlarged spleen	Katnal2<em1(IMPC)Tcp>/Katnal2<em1(IMPC)Tcp>	C57BL/6N-Katnal2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408460	M	MP:0001925	male infertility	Katnal2<em1(IMPC)Tcp>/Katnal2<em1(IMPC)Tcp>	C57BL/6N-Katnal2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408460	M	MP:0000702	enlarged lymph nodes	Katnal2<em1(IMPC)Tcp>/Katnal2<em1(IMPC)Tcp>	C57BL/6N-Katnal2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408460	F	MP:0000692	small spleen	Katnal2<em1(IMPC)Tcp>/Katnal2<em1(IMPC)Tcp>	C57BL/6N-Katnal2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408460	M	MP:0003883	enlarged stomach	Katnal2<em1(IMPC)Tcp>/Katnal2<em1(IMPC)Tcp>	C57BL/6N-Katnal2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408460	F	MP:0000220	increased monocyte cell number	Katnal2<em1(IMPC)Tcp>/Katnal2<em1(IMPC)Tcp>	C57BL/6N-Katnal2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408460	F	MP:0001120	abnormal uterus morphology	Katnal2<em1(IMPC)Tcp>/Katnal2<em1(IMPC)Tcp>	C57BL/6N-Katnal2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408460	F	MP:0001944	abnormal pancreas morphology	Katnal2<em1(IMPC)Tcp>/Katnal2<em1(IMPC)Tcp>	C57BL/6N-Katnal2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408460	F	MP:0002968	increased circulating alkaline phosphatase level	Katnal2<em1(IMPC)Tcp>/Katnal2<em1(IMPC)Tcp>	C57BL/6N-Katnal2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408461	F	MP:0001120	abnormal uterus morphology	Kbtbd11<em1(IMPC)Wtsi>/Kbtbd11<em1(IMPC)Wtsi>	C57BL/6N-Kbtbd11<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408461	M	MP:0001262	decreased body weight	Kbtbd11<em1(IMPC)Wtsi>/Kbtbd11<em1(IMPC)Wtsi>	C57BL/6N-Kbtbd11<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408461	M	MP:0002059	abnormal seminal vesicle morphology	Kbtbd11<em1(IMPC)Wtsi>/Kbtbd11<em1(IMPC)Wtsi>	C57BL/6N-Kbtbd11<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408461	M	MP:0001147	small testis	Kbtbd11<em1(IMPC)Wtsi>/Kbtbd11<em1(IMPC)Wtsi>	C57BL/6N-Kbtbd11<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408461	F	MP:0009709	hydrometra	Kbtbd11<em1(IMPC)Wtsi>/Kbtbd11<em1(IMPC)Wtsi>	C57BL/6N-Kbtbd11<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408461	M	MP:0001146	abnormal testis morphology	Kbtbd11<em1(IMPC)Wtsi>/Kbtbd11<em1(IMPC)Wtsi>	C57BL/6N-Kbtbd11<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408461	F	MP:0000689	abnormal spleen morphology	Kbtbd11<em1(IMPC)Wtsi>/Kbtbd11<em1(IMPC)Wtsi>	C57BL/6N-Kbtbd11<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408461	F	MP:0000691	enlarged spleen	Kbtbd11<em1(IMPC)Wtsi>/Kbtbd11<em1(IMPC)Wtsi>	C57BL/6N-Kbtbd11<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408461	F	MP:0020421	increased freezing behavior	Kbtbd11<em1(IMPC)Wtsi>/Kbtbd11<em1(IMPC)Wtsi>	C57BL/6N-Kbtbd11<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408462	F	MP:0001512	trunk curl	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	F	MP:0000063	decreased bone mineral density	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	F	MP:0000220	increased monocyte cell number	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	F	MP:0005565	increased blood urea nitrogen level	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	F	MP:0010025	decreased total body fat amount	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	F	MP:0005016	decreased lymphocyte cell number	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	M	MP:0001406	abnormal gait	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	F	MP:0001402	decreased locomotor activity	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	F	MP:0002066	abnormal motor capabilities/coordination/movement	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	F	MP:0000219	increased neutrophil cell number	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	F	MP:0002590	increased mean corpuscular volume	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	F	MP:0002941	increased circulating alanine transaminase level	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	M	MP:0002968	increased circulating alkaline phosphatase level	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	F	MP:0000745	tremors	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	F	MP:0010124	decreased bone mineral content	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408462	F	MP:0001523	impaired righting response	Kcne1<tm1b(EUCOMM)Hmgu>/Kcne1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcne1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6408463	F	MP:0000222	decreased neutrophil cell number	Kcnj6<em1(IMPC)H>/Kcnj6<em1(IMPC)H>	C57BL/6N-Kcnj6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408463	M	MP:0001523	impaired righting response	Kcnj6<em1(IMPC)H>/Kcnj6<em1(IMPC)H>	C57BL/6N-Kcnj6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408463	F	MP:0008806	increased circulating amylase level	Kcnj6<em1(IMPC)H>/Kcnj6<em1(IMPC)H>	C57BL/6N-Kcnj6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408463	F	MP:0001415	increased exploration in new environment	Kcnj6<em1(IMPC)H>/Kcnj6<em1(IMPC)H>	C57BL/6N-Kcnj6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408465	F	MP:0000692	small spleen	Kdm3a<em1(IMPC)Mbp>/Kdm3a<em1(IMPC)Mbp>	C57BL/6N-Kdm3a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408465	M	MP:0000266	abnormal heart morphology	Kdm3a<em1(IMPC)Mbp>/Kdm3a<em1(IMPC)Mbp>	C57BL/6N-Kdm3a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408465	M	MP:0001399	hyperactivity	Kdm3a<em1(IMPC)Mbp>/Kdm3a<em1(IMPC)Mbp>	C57BL/6N-Kdm3a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408465	F	MP:0010124	decreased bone mineral content	Kdm3a<em1(IMPC)Mbp>/Kdm3a<em1(IMPC)Mbp>	C57BL/6N-Kdm3a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408465	M	MP:0001925	male infertility	Kdm3a<em1(IMPC)Mbp>/Kdm3a<em1(IMPC)Mbp>	C57BL/6N-Kdm3a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408465	M	MP:0002060	abnormal skin morphology	Kdm3a<em1(IMPC)Mbp>/Kdm3a<em1(IMPC)Mbp>	C57BL/6N-Kdm3a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408465	F	MP:0004924	abnormal behavior	Kdm3a<em1(IMPC)Mbp>/Kdm3a<em1(IMPC)Mbp>	C57BL/6N-Kdm3a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408465	M	MP:0000274	enlarged heart	Kdm3a<em1(IMPC)Mbp>/Kdm3a<em1(IMPC)Mbp>	C57BL/6N-Kdm3a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408465	F	MP:0020870	decreased thigmotaxis	Kdm3a<em1(IMPC)Mbp>/Kdm3a<em1(IMPC)Mbp>	C57BL/6N-Kdm3a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408468	F	MP:0002102	abnormal ear morphology	Klhdc7b<em1(IMPC)H>/Klhdc7b<em1(IMPC)H>	C57BL/6N-Klhdc7b<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408468	F	MP:0005011	increased eosinophil cell number	Klhdc7b<em1(IMPC)H>/Klhdc7b<em1(IMPC)H>	C57BL/6N-Klhdc7b<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408468	F	MP:0005016	decreased lymphocyte cell number	Klhdc7b<em1(IMPC)H>/Klhdc7b<em1(IMPC)H>	C57BL/6N-Klhdc7b<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408468	F	MP:0001392	abnormal locomotor behavior	Klhdc7b<em1(IMPC)H>/Klhdc7b<em1(IMPC)H>	C57BL/6N-Klhdc7b<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408469	F	MP:0001312	abnormal cornea morphology	Klhl5<tm1b(EUCOMM)Hmgu>/Klhl5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Klhl5<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408469	M	MP:0002135	abnormal kidney morphology	Klhl5<tm1b(EUCOMM)Hmgu>/Klhl5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Klhl5<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408469	F	MP:0001303	abnormal lens morphology	Klhl5<tm1b(EUCOMM)Hmgu>/Klhl5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Klhl5<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408469	F	MP:0001552	increased circulating triglyceride level	Klhl5<tm1b(EUCOMM)Hmgu>/Klhl5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Klhl5<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408469	M	MP:0000150	abnormal rib morphology	Klhl5<tm1b(EUCOMM)Hmgu>/Klhl5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Klhl5<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408471	M	MP:0002941	increased circulating alanine transaminase level	Klk13<em1(IMPC)Ccpcz>/Klk13<em1(IMPC)Ccpcz>	C57BL/6N-Klk13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408471	M	MP:0002092	abnormal eye morphology	Klk13<em1(IMPC)Ccpcz>/Klk13<em1(IMPC)Ccpcz>	C57BL/6N-Klk13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408471	M	MP:0001297	microphthalmia	Klk13<em1(IMPC)Ccpcz>/Klk13<em1(IMPC)Ccpcz>	C57BL/6N-Klk13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408472	M	MP:0002160	abnormal reproductive system morphology	Klrc3<em1(IMPC)Wtsi>/Klrc3<em1(IMPC)Wtsi>	C57BL/6N-Klrc3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408474	M	MP:0001925	male infertility	L2hgdh<em1(IMPC)Tcp>/L2hgdh<em1(IMPC)Tcp>	C57BL/6N-L2hgdh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408474	F	MP:0001417	decreased exploration in new environment	L2hgdh<em1(IMPC)Tcp>/L2hgdh<em1(IMPC)Tcp>	C57BL/6N-L2hgdh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408474	F	MP:0002092	abnormal eye morphology	L2hgdh<em1(IMPC)Tcp>/L2hgdh<em1(IMPC)Tcp>	C57BL/6N-L2hgdh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408475	M	MP:0004924	abnormal behavior	Lamtor4<em1(IMPC)Ccpcz>/Lamtor4<+>	C57BL/6N-Lamtor4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408475	M	MP:0020870	decreased thigmotaxis	Lamtor4<em1(IMPC)Ccpcz>/Lamtor4<+>	C57BL/6N-Lamtor4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408475	M	MP:0005355	enlarged thyroid gland	Lamtor4<em1(IMPC)Ccpcz>/Lamtor4<+>	C57BL/6N-Lamtor4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408475	M	MP:0001399	hyperactivity	Lamtor4<em1(IMPC)Ccpcz>/Lamtor4<+>	C57BL/6N-Lamtor4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408475	M	MP:0000681	abnormal thyroid gland morphology	Lamtor4<em1(IMPC)Ccpcz>/Lamtor4<+>	C57BL/6N-Lamtor4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408477	M	MP:0001486	abnormal startle reflex	Lat<em1(IMPC)Ics>/Lat<em1(IMPC)Ics>	C57BL/6N-Lat<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408477	F	MP:0002699	abnormal vitreous body morphology	Lat<em1(IMPC)Ics>/Lat<em1(IMPC)Ics>	C57BL/6N-Lat<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408479	F	MP:0002874	decreased hemoglobin content	Lats1<em1(IMPC)H>/Lats1<em1(IMPC)H>	C57BL/6NTac-Lats1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408479	F	MP:0002941	increased circulating alanine transaminase level	Lats1<em1(IMPC)H>/Lats1<em1(IMPC)H>	C57BL/6NTac-Lats1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408479	F	MP:0010052	increased grip strength	Lats1<em1(IMPC)H>/Lats1<em1(IMPC)H>	C57BL/6NTac-Lats1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408480	F	MP:0005344	increased circulating bilirubin level	Lca5l<em1(IMPC)Ics>/Lca5l<em1(IMPC)Ics>	C57BL/6N-Lca5l<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408480	M	MP:0001925	male infertility	Lca5l<em1(IMPC)Ics>/Lca5l<em1(IMPC)Ics>	C57BL/6N-Lca5l<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408481	M	MP:0002941	increased circulating alanine transaminase level	Lclat1<em1(IMPC)Mbp>/Lclat1<em1(IMPC)Mbp>	C57BL/6N-Lclat1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408481	F	MP:0002968	increased circulating alkaline phosphatase level	Lclat1<em1(IMPC)Mbp>/Lclat1<em1(IMPC)Mbp>	C57BL/6N-Lclat1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408482	F	MP:0011239	abnormal skin coloration	Ldlrad1<tm1b(KOMP)Wtsi>/Ldlrad1<tm1b(KOMP)Wtsi>	C57BL/6N-Ldlrad1<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408484	M	MP:0002060	abnormal skin morphology	Lgi3<em1(IMPC)Mbp>/Lgi3<em1(IMPC)Mbp>	C57BL/6N-Lgi3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408484	M	MP:0002135	abnormal kidney morphology	Lgi3<em1(IMPC)Mbp>/Lgi3<em1(IMPC)Mbp>	C57BL/6N-Lgi3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408484	M	MP:0000689	abnormal spleen morphology	Lgi3<em1(IMPC)Mbp>/Lgi3<em1(IMPC)Mbp>	C57BL/6N-Lgi3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408484	M	MP:0001200	thick skin	Lgi3<em1(IMPC)Mbp>/Lgi3<em1(IMPC)Mbp>	C57BL/6N-Lgi3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408484	M	MP:0003068	enlarged kidney	Lgi3<em1(IMPC)Mbp>/Lgi3<em1(IMPC)Mbp>	C57BL/6N-Lgi3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408484	M	MP:0000691	enlarged spleen	Lgi3<em1(IMPC)Mbp>/Lgi3<em1(IMPC)Mbp>	C57BL/6N-Lgi3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408486	M	MP:0001157	small seminal vesicle	Lsm8<em1(IMPC)Mbp>/Lsm8<+>	C57BL/6N-Lsm8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408486	F	MP:0005553	increased circulating creatinine level	Lsm8<em1(IMPC)Mbp>/Lsm8<+>	C57BL/6N-Lsm8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408486	M	MP:0002059	abnormal seminal vesicle morphology	Lsm8<em1(IMPC)Mbp>/Lsm8<+>	C57BL/6N-Lsm8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408486	F	MP:0000702	enlarged lymph nodes	Lsm8<em1(IMPC)Mbp>/Lsm8<+>	C57BL/6N-Lsm8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408486	F	MP:0002339	abnormal lymph node morphology	Lsm8<em1(IMPC)Mbp>/Lsm8<+>	C57BL/6N-Lsm8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408486	F	MP:0002965	increased circulating serum albumin level	Lsm8<em1(IMPC)Mbp>/Lsm8<+>	C57BL/6N-Lsm8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408486	F	MP:0002941	increased circulating alanine transaminase level	Lsm8<em1(IMPC)Mbp>/Lsm8<+>	C57BL/6N-Lsm8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408486	F	MP:0005565	increased blood urea nitrogen level	Lsm8<em1(IMPC)Mbp>/Lsm8<+>	C57BL/6N-Lsm8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408486	F	MP:0005568	increased circulating total protein level	Lsm8<em1(IMPC)Mbp>/Lsm8<+>	C57BL/6N-Lsm8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408488	M	MP:0000599	enlarged liver	Luc7l<em1(IMPC)Mbp>/Luc7l<em1(IMPC)Mbp>	C57BL/6N-Luc7l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408488	F	MP:0001297	microphthalmia	Luc7l<em1(IMPC)Mbp>/Luc7l<em1(IMPC)Mbp>	C57BL/6N-Luc7l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408488	F	MP:0002188	small heart	Luc7l<em1(IMPC)Mbp>/Luc7l<em1(IMPC)Mbp>	C57BL/6N-Luc7l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408488	F	MP:0001293	anophthalmia	Luc7l<em1(IMPC)Mbp>/Luc7l<em1(IMPC)Mbp>	C57BL/6N-Luc7l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408488	F	MP:0003131	increased erythrocyte cell number	Luc7l<em1(IMPC)Mbp>/Luc7l<em1(IMPC)Mbp>	C57BL/6N-Luc7l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408488	M	MP:0002075	abnormal coat/hair pigmentation	Luc7l<em1(IMPC)Mbp>/Luc7l<em1(IMPC)Mbp>	C57BL/6N-Luc7l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408488	F	MP:0002989	small kidney	Luc7l<em1(IMPC)Mbp>/Luc7l<em1(IMPC)Mbp>	C57BL/6N-Luc7l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408488	F	MP:0002092	abnormal eye morphology	Luc7l<em1(IMPC)Mbp>/Luc7l<em1(IMPC)Mbp>	C57BL/6N-Luc7l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408488	M	MP:0002339	abnormal lymph node morphology	Luc7l<em1(IMPC)Mbp>/Luc7l<em1(IMPC)Mbp>	C57BL/6N-Luc7l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408488	M	MP:0000702	enlarged lymph nodes	Luc7l<em1(IMPC)Mbp>/Luc7l<em1(IMPC)Mbp>	C57BL/6N-Luc7l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	F	MP:0004832	enlarged ovary	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	M	MP:0002989	small kidney	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	F	MP:0002699	abnormal vitreous body morphology	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	F	MP:0005344	increased circulating bilirubin level	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	F	MP:0000601	small liver	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	M	MP:0009552	urinary bladder obstruction	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	F	MP:0000692	small spleen	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	F	MP:0001126	abnormal ovary morphology	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	M	MP:0002135	abnormal kidney morphology	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	F	MP:0000598	abnormal liver morphology	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	F	MP:0020421	increased freezing behavior	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	F	MP:0001304	cataract	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	F	MP:0010052	increased grip strength	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408489	M	MP:0003068	enlarged kidney	Maf<em1(IMPC)Mbp>/Maf<+>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408490	F	MP:0003984	embryonic growth retardation	Maf<em1(IMPC)Mbp>/Maf<em1(IMPC)Mbp>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408490	F	MP:0001614	abnormal blood vessel morphology	Maf<em1(IMPC)Mbp>/Maf<em1(IMPC)Mbp>	C57BL/6N-Maf<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408491	M	MP:0010579	increased heart left ventricle size	Man1b1<em1(IMPC)Bay>/Man1b1<+>	C57BL/6N-Man1b1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408492	M	MP:0003394	increased cardiac output	Man2a1<em1(IMPC)Hmgu>/Man2a1<em1(IMPC)Hmgu>	C57BL/6N-Man2a1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408492	M	MP:0003179	thrombocytopenia	Man2a1<em1(IMPC)Hmgu>/Man2a1<em1(IMPC)Hmgu>	C57BL/6N-Man2a1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408492	M	MP:0002591	decreased mean corpuscular volume	Man2a1<em1(IMPC)Hmgu>/Man2a1<em1(IMPC)Hmgu>	C57BL/6N-Man2a1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408492	F	MP:0002966	decreased circulating alkaline phosphatase level	Man2a1<em1(IMPC)Hmgu>/Man2a1<em1(IMPC)Hmgu>	C57BL/6N-Man2a1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408492	F	MP:0002699	abnormal vitreous body morphology	Man2a1<em1(IMPC)Hmgu>/Man2a1<em1(IMPC)Hmgu>	C57BL/6N-Man2a1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408492	M	MP:0002599	increased mean platelet volume	Man2a1<em1(IMPC)Hmgu>/Man2a1<em1(IMPC)Hmgu>	C57BL/6N-Man2a1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408492	M	MP:0004151	decreased circulating iron level	Man2a1<em1(IMPC)Hmgu>/Man2a1<em1(IMPC)Hmgu>	C57BL/6N-Man2a1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408492	M	MP:0005344	increased circulating bilirubin level	Man2a1<em1(IMPC)Hmgu>/Man2a1<em1(IMPC)Hmgu>	C57BL/6N-Man2a1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408493	F	MP:0002590	increased mean corpuscular volume	Marchf8<em2(IMPC)Ccpcz>/Marchf8<em2(IMPC)Ccpcz>	C57BL/6N-Marchf8<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408493	F	MP:0005012	decreased eosinophil cell number	Marchf8<em2(IMPC)Ccpcz>/Marchf8<em2(IMPC)Ccpcz>	C57BL/6N-Marchf8<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408493	M	MP:0010935	increased airway resistance	Marchf8<em2(IMPC)Ccpcz>/Marchf8<em2(IMPC)Ccpcz>	C57BL/6N-Marchf8<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408494	F	MP:0000063	decreased bone mineral density	Mavs<em1(IMPC)Mbp>/Mavs<em1(IMPC)Mbp>	C57BL/6N-Mavs<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408495	F	MP:0001417	decreased exploration in new environment	Maz<em1(IMPC)Ics>/Maz<+>	C57BL/6N-Maz<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408495	M	MP:0000432	abnormal head morphology	Maz<em1(IMPC)Ics>/Maz<+>	C57BL/6N-Maz<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408497	M	MP:0020421	increased freezing behavior	Mex3b<tm1b(KOMP)Wtsi>/Mex3b<tm1b(KOMP)Wtsi>	C57BL/6N-Mex3b<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408497	M	MP:0004599	abnormal vertebral arch morphology	Mex3b<tm1b(KOMP)Wtsi>/Mex3b<tm1b(KOMP)Wtsi>	C57BL/6N-Mex3b<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408497	F	MP:0001126	abnormal ovary morphology	Mex3b<tm1b(KOMP)Wtsi>/Mex3b<tm1b(KOMP)Wtsi>	C57BL/6N-Mex3b<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408497	M	MP:0001262	decreased body weight	Mex3b<tm1b(KOMP)Wtsi>/Mex3b<tm1b(KOMP)Wtsi>	C57BL/6N-Mex3b<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408497	M	MP:0002100	abnormal tooth morphology	Mex3b<tm1b(KOMP)Wtsi>/Mex3b<tm1b(KOMP)Wtsi>	C57BL/6N-Mex3b<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408497	M	MP:0003036	vertebral transformation	Mex3b<tm1b(KOMP)Wtsi>/Mex3b<tm1b(KOMP)Wtsi>	C57BL/6N-Mex3b<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408497	M	MP:0000137	abnormal vertebrae morphology	Mex3b<tm1b(KOMP)Wtsi>/Mex3b<tm1b(KOMP)Wtsi>	C57BL/6N-Mex3b<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408499	M	MP:0003068	enlarged kidney	Mink1<em1(IMPC)Tcp>/Mink1<em1(IMPC)Tcp>	C57BL/6N-Mink1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408499	F	MP:0001297	microphthalmia	Mink1<em1(IMPC)Tcp>/Mink1<em1(IMPC)Tcp>	C57BL/6N-Mink1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408499	F	MP:0002100	abnormal tooth morphology	Mink1<em1(IMPC)Tcp>/Mink1<em1(IMPC)Tcp>	C57BL/6N-Mink1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408499	M	MP:0002060	abnormal skin morphology	Mink1<em1(IMPC)Tcp>/Mink1<em1(IMPC)Tcp>	C57BL/6N-Mink1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408499	M	MP:0000157	abnormal sternum morphology	Mink1<em1(IMPC)Tcp>/Mink1<em1(IMPC)Tcp>	C57BL/6N-Mink1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408499	M	MP:0000702	enlarged lymph nodes	Mink1<em1(IMPC)Tcp>/Mink1<em1(IMPC)Tcp>	C57BL/6N-Mink1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408499	F	MP:0002637	small uterus	Mink1<em1(IMPC)Tcp>/Mink1<em1(IMPC)Tcp>	C57BL/6N-Mink1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408500	F	MP:0002965	increased circulating serum albumin level	Mipep<em1(IMPC)Mbp>/Mipep<+>	C57BL/6N-Mipep<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408502	M	MP:0005343	increased circulating aspartate transaminase level	Mmd<em1(IMPC)Hmgu>/Mmd<em1(IMPC)Hmgu>	C57BL/6N-Mmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408502	F	MP:0001325	abnormal retina morphology	Mmd<em1(IMPC)Hmgu>/Mmd<em1(IMPC)Hmgu>	C57BL/6N-Mmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408502	F	MP:0001258	decreased body length	Mmd<em1(IMPC)Hmgu>/Mmd<em1(IMPC)Hmgu>	C57BL/6N-Mmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408502	F	MP:0002968	increased circulating alkaline phosphatase level	Mmd<em1(IMPC)Hmgu>/Mmd<em1(IMPC)Hmgu>	C57BL/6N-Mmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408502	M	MP:0010052	increased grip strength	Mmd<em1(IMPC)Hmgu>/Mmd<em1(IMPC)Hmgu>	C57BL/6N-Mmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408503	M	MP:0005178	increased circulating cholesterol level	Mocos<em2(IMPC)Ics>/Mocos<+>	C57BL/6N-Mocos<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408503	M	MP:0010024	increased total body fat amount	Mocos<em2(IMPC)Ics>/Mocos<+>	C57BL/6N-Mocos<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408504	M	MP:0001417	decreased exploration in new environment	Mrps12<em1(IMPC)Bay>/Mrps12<+>	C57BL/6N-Mrps12<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408506	M	MP:0010124	decreased bone mineral content	Msl1<em1(IMPC)Wtsi>/Msl1<+>	C57BL/6N-Msl1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408508	M	MP:0003068	enlarged kidney	Msto1<em1(IMPC)Tcp>/Msto1<+>	C57BL/6N-Msto1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408508	M	MP:0001552	increased circulating triglyceride level	Msto1<em1(IMPC)Tcp>/Msto1<+>	C57BL/6N-Msto1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408508	M	MP:0000702	enlarged lymph nodes	Msto1<em1(IMPC)Tcp>/Msto1<+>	C57BL/6N-Msto1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408508	F	MP:0000692	small spleen	Msto1<em1(IMPC)Tcp>/Msto1<+>	C57BL/6N-Msto1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408508	M	MP:0002059	abnormal seminal vesicle morphology	Msto1<em1(IMPC)Tcp>/Msto1<+>	C57BL/6N-Msto1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408511	F	MP:0003733	abnormal retina inner nuclear layer morphology	Mx2<em1(IMPC)Ics>/Mx2<em1(IMPC)Ics>	C57BL/6N-Mx2<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408511	F	MP:0002699	abnormal vitreous body morphology	Mx2<em1(IMPC)Ics>/Mx2<em1(IMPC)Ics>	C57BL/6N-Mx2<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408511	M	MP:0001486	abnormal startle reflex	Mx2<em1(IMPC)Ics>/Mx2<em1(IMPC)Ics>	C57BL/6N-Mx2<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408511	M	MP:0005344	increased circulating bilirubin level	Mx2<em1(IMPC)Ics>/Mx2<em1(IMPC)Ics>	C57BL/6N-Mx2<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408513	M	MP:0005179	decreased circulating cholesterol level	Myh7b<tm1a(KOMP)Wtsi>/Myh7b<tm1a(KOMP)Wtsi>	C57BL/6N-Myh7b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408513	M	MP:0010067	increased red blood cell distribution width	Myh7b<tm1a(KOMP)Wtsi>/Myh7b<tm1a(KOMP)Wtsi>	C57BL/6N-Myh7b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408515	M	MP:0000221	decreased leukocyte cell number	Myo6<em1(IMPC)Tcp>/Myo6<em1(IMPC)Tcp>	C57BL/6N-Myo6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408515	M	MP:0000157	abnormal sternum morphology	Myo6<em1(IMPC)Tcp>/Myo6<em1(IMPC)Tcp>	C57BL/6N-Myo6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408515	M	MP:0010025	decreased total body fat amount	Myo6<em1(IMPC)Tcp>/Myo6<em1(IMPC)Tcp>	C57BL/6N-Myo6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408515	M	MP:0001489	decreased startle reflex	Myo6<em1(IMPC)Tcp>/Myo6<em1(IMPC)Tcp>	C57BL/6N-Myo6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408515	M	MP:0003960	increased lean body mass	Myo6<em1(IMPC)Tcp>/Myo6<em1(IMPC)Tcp>	C57BL/6N-Myo6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408515	F	MP:0010053	decreased grip strength	Myo6<em1(IMPC)Tcp>/Myo6<em1(IMPC)Tcp>	C57BL/6N-Myo6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408515	F	MP:0005628	decreased circulating potassium level	Myo6<em1(IMPC)Tcp>/Myo6<em1(IMPC)Tcp>	C57BL/6N-Myo6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408515	M	MP:0000470	abnormal stomach morphology	Myo6<em1(IMPC)Tcp>/Myo6<em1(IMPC)Tcp>	C57BL/6N-Myo6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408515	M	MP:0011874	enlarged urinary bladder	Myo6<em1(IMPC)Tcp>/Myo6<em1(IMPC)Tcp>	C57BL/6N-Myo6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408515	F	MP:0001120	abnormal uterus morphology	Myo6<em1(IMPC)Tcp>/Myo6<em1(IMPC)Tcp>	C57BL/6N-Myo6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408515	M	MP:0002968	increased circulating alkaline phosphatase level	Myo6<em1(IMPC)Tcp>/Myo6<em1(IMPC)Tcp>	C57BL/6N-Myo6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408515	F	MP:0001258	decreased body length	Myo6<em1(IMPC)Tcp>/Myo6<em1(IMPC)Tcp>	C57BL/6N-Myo6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408515	M	MP:0002590	increased mean corpuscular volume	Myo6<em1(IMPC)Tcp>/Myo6<em1(IMPC)Tcp>	C57BL/6N-Myo6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408517	F	MP:0005634	decreased circulating sodium level	Mzb1<em1(IMPC)Ccpcz>/Mzb1<em1(IMPC)Ccpcz>	C57BL/6N-Mzb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408518	M	MP:0001262	decreased body weight	Naa38<em1(IMPC)Ccpcz>/Naa38<+>	C57BL/6N-Naa38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408518	F	MP:0001120	abnormal uterus morphology	Naa38<em1(IMPC)Ccpcz>/Naa38<+>	C57BL/6N-Naa38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408518	F	MP:0000702	enlarged lymph nodes	Naa38<em1(IMPC)Ccpcz>/Naa38<+>	C57BL/6N-Naa38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408518	M	MP:0000274	enlarged heart	Naa38<em1(IMPC)Ccpcz>/Naa38<+>	C57BL/6N-Naa38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408518	F	MP:0000538	abnormal urinary bladder morphology	Naa38<em1(IMPC)Ccpcz>/Naa38<+>	C57BL/6N-Naa38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408518	F	MP:0002339	abnormal lymph node morphology	Naa38<em1(IMPC)Ccpcz>/Naa38<+>	C57BL/6N-Naa38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408518	F	MP:0009552	urinary bladder obstruction	Naa38<em1(IMPC)Ccpcz>/Naa38<+>	C57BL/6N-Naa38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408518	F	MP:0009709	hydrometra	Naa38<em1(IMPC)Ccpcz>/Naa38<+>	C57BL/6N-Naa38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408518	F	MP:0000703	abnormal thymus morphology	Naa38<em1(IMPC)Ccpcz>/Naa38<+>	C57BL/6N-Naa38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408518	M	MP:0000266	abnormal heart morphology	Naa38<em1(IMPC)Ccpcz>/Naa38<+>	C57BL/6N-Naa38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408518	F	MP:0000709	enlarged thymus	Naa38<em1(IMPC)Ccpcz>/Naa38<+>	C57BL/6N-Naa38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408520	M	MP:0002092	abnormal eye morphology	Naaladl2<em1(IMPC)Tcp>/Naaladl2<em1(IMPC)Tcp>	C57BL/6N-Naaladl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408521	M	MP:0008528	polycystic kidney	Nacc1<em1(IMPC)Hmgu>/Nacc1<em1(IMPC)Hmgu>	C57BL/6N-Nacc1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408521	F	MP:0001284	absent vibrissae	Nacc1<em1(IMPC)Hmgu>/Nacc1<em1(IMPC)Hmgu>	C57BL/6N-Nacc1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408521	F	MP:0010053	decreased grip strength	Nacc1<em1(IMPC)Hmgu>/Nacc1<em1(IMPC)Hmgu>	C57BL/6N-Nacc1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408521	M	MP:0002764	short tibia	Nacc1<em1(IMPC)Hmgu>/Nacc1<em1(IMPC)Hmgu>	C57BL/6N-Nacc1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408521	F	MP:0002590	increased mean corpuscular volume	Nacc1<em1(IMPC)Hmgu>/Nacc1<em1(IMPC)Hmgu>	C57BL/6N-Nacc1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408521	M	MP:0010124	decreased bone mineral content	Nacc1<em1(IMPC)Hmgu>/Nacc1<em1(IMPC)Hmgu>	C57BL/6N-Nacc1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408521	F	MP:0009709	hydrometra	Nacc1<em1(IMPC)Hmgu>/Nacc1<em1(IMPC)Hmgu>	C57BL/6N-Nacc1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408521	F	MP:0005293	impaired glucose tolerance	Nacc1<em1(IMPC)Hmgu>/Nacc1<em1(IMPC)Hmgu>	C57BL/6N-Nacc1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408522	F	MP:0011239	abnormal skin coloration	Nanos2<em1(IMPC)Bay>/Nanos2<em1(IMPC)Bay>	C57BL/6N-Nanos2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408522	M	MP:0001925	male infertility	Nanos2<em1(IMPC)Bay>/Nanos2<em1(IMPC)Bay>	C57BL/6N-Nanos2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408522	F	MP:0005565	increased blood urea nitrogen level	Nanos2<em1(IMPC)Bay>/Nanos2<em1(IMPC)Bay>	C57BL/6N-Nanos2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408524	F	MP:0003795	abnormal bone structure	Ndufa10<tm1e.1(EUCOMM)Hmgu>/Ndufa10<+>	C57BL/6N-Ndufa10<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408526	M	MP:0000367	abnormal coat/ hair morphology	Nedd1<em1(IMPC)H>/Nedd1<+>	C57BL/6NTac-Nedd1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408526	F	MP:0010088	decreased circulating fructosamine level	Nedd1<em1(IMPC)H>/Nedd1<+>	C57BL/6NTac-Nedd1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408528	M	MP:0000745	tremors	Neto2<em1(IMPC)Hmgu>/Neto2<em1(IMPC)Hmgu>	C57BL/6N-Neto2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408528	M	MP:0008806	increased circulating amylase level	Neto2<em1(IMPC)Hmgu>/Neto2<em1(IMPC)Hmgu>	C57BL/6N-Neto2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408528	M	MP:0011886	increased circulating lipase level	Neto2<em1(IMPC)Hmgu>/Neto2<em1(IMPC)Hmgu>	C57BL/6N-Neto2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408529	M	MP:0001510	abnormal coat appearance	Neurod2<em1(IMPC)Hmgu>/Neurod2<+>	C57BL/6N-Neurod2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408529	F	MP:0001303	abnormal lens morphology	Neurod2<em1(IMPC)Hmgu>/Neurod2<+>	C57BL/6N-Neurod2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408530	F	MP:0010024	increased total body fat amount	Neurod2<em1(IMPC)Hmgu>/Neurod2<em1(IMPC)Hmgu>	C57BL/6N-Neurod2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408530	M	MP:0001510	abnormal coat appearance	Neurod2<em1(IMPC)Hmgu>/Neurod2<em1(IMPC)Hmgu>	C57BL/6N-Neurod2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408530	F	MP:0009142	decreased prepulse inhibition	Neurod2<em1(IMPC)Hmgu>/Neurod2<em1(IMPC)Hmgu>	C57BL/6N-Neurod2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408530	F	MP:0001314	cornea opacity	Neurod2<em1(IMPC)Hmgu>/Neurod2<em1(IMPC)Hmgu>	C57BL/6N-Neurod2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408530	F	MP:0002764	short tibia	Neurod2<em1(IMPC)Hmgu>/Neurod2<em1(IMPC)Hmgu>	C57BL/6N-Neurod2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408530	F	MP:0001392	abnormal locomotor behavior	Neurod2<em1(IMPC)Hmgu>/Neurod2<em1(IMPC)Hmgu>	C57BL/6N-Neurod2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408531	M	MP:0001399	hyperactivity	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0000157	abnormal sternum morphology	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0003961	decreased lean body mass	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0009454	impaired contextual conditioning behavior	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0001552	increased circulating triglyceride level	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0010024	increased total body fat amount	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0010124	decreased bone mineral content	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0010067	increased red blood cell distribution width	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0000220	increased monocyte cell number	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0005011	increased eosinophil cell number	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0002606	increased basophil cell number	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0002590	increased mean corpuscular volume	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0005565	increased blood urea nitrogen level	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0001258	decreased body length	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0005561	increased mean corpuscular hemoglobin	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0011874	enlarged urinary bladder	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408531	M	MP:0000692	small spleen	Nexmif<em1(IMPC)Tcp>/Y	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408532	F	MP:0001392	abnormal locomotor behavior	Nfatc2ip<em1(IMPC)Ics>/Nfatc2ip<em1(IMPC)Ics>	C57BL/6N-Nfatc2ip<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408532	M	MP:0005011	increased eosinophil cell number	Nfatc2ip<em1(IMPC)Ics>/Nfatc2ip<em1(IMPC)Ics>	C57BL/6N-Nfatc2ip<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408535	F	MP:0003731	abnormal retina outer nuclear layer morphology	Nlrp2<tm1b(KOMP)Wtsi>/Nlrp2<tm1b(KOMP)Wtsi>	C57BL/6N-Nlrp2<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408535	F	MP:0011964	increased total retina thickness	Nlrp2<tm1b(KOMP)Wtsi>/Nlrp2<tm1b(KOMP)Wtsi>	C57BL/6N-Nlrp2<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408537	M	MP:0001406	abnormal gait	Nnt<em1(IMPC)H>/Nnt<em1(IMPC)H>	C57BL/6N-Nnt<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408538	M	MP:0001146	abnormal testis morphology	Nod2<em1(IMPC)Mbp>/Nod2<em1(IMPC)Mbp>	C57BL/6N-Nod2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408538	F	MP:0001944	abnormal pancreas morphology	Nod2<em1(IMPC)Mbp>/Nod2<em1(IMPC)Mbp>	C57BL/6N-Nod2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408538	M	MP:0001364	decreased anxiety-related response	Nod2<em1(IMPC)Mbp>/Nod2<em1(IMPC)Mbp>	C57BL/6N-Nod2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408538	F	MP:0002339	abnormal lymph node morphology	Nod2<em1(IMPC)Mbp>/Nod2<em1(IMPC)Mbp>	C57BL/6N-Nod2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408538	M	MP:0020870	decreased thigmotaxis	Nod2<em1(IMPC)Mbp>/Nod2<em1(IMPC)Mbp>	C57BL/6N-Nod2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408538	F	MP:0000702	enlarged lymph nodes	Nod2<em1(IMPC)Mbp>/Nod2<em1(IMPC)Mbp>	C57BL/6N-Nod2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408539	F	MP:0005553	increased circulating creatinine level	Nox4<em1(IMPC)Mbp>/Nox4<em1(IMPC)Mbp>	C57BL/6N-Nox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408541	F	MP:0000689	abnormal spleen morphology	Nsmce1<em1(IMPC)Wtsi>/Nsmce1<+>	C57BL/6N-Nsmce1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408541	F	MP:0001120	abnormal uterus morphology	Nsmce1<em1(IMPC)Wtsi>/Nsmce1<+>	C57BL/6N-Nsmce1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408541	F	MP:0009709	hydrometra	Nsmce1<em1(IMPC)Wtsi>/Nsmce1<+>	C57BL/6N-Nsmce1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408541	F	MP:0000691	enlarged spleen	Nsmce1<em1(IMPC)Wtsi>/Nsmce1<+>	C57BL/6N-Nsmce1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408541	M	MP:0001552	increased circulating triglyceride level	Nsmce1<em1(IMPC)Wtsi>/Nsmce1<+>	C57BL/6N-Nsmce1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408542	F	MP:0000219	increased neutrophil cell number	Nsun5<tm2b(EUCOMM)Wtsi>/Nsun5<tm2b(EUCOMM)Wtsi>	C57BL/6N-Nsun5<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6408542	F	MP:0004953	decreased spleen weight	Nsun5<tm2b(EUCOMM)Wtsi>/Nsun5<tm2b(EUCOMM)Wtsi>	C57BL/6N-Nsun5<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6408542	F	MP:0005016	decreased lymphocyte cell number	Nsun5<tm2b(EUCOMM)Wtsi>/Nsun5<tm2b(EUCOMM)Wtsi>	C57BL/6N-Nsun5<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6408542	M	MP:0010392	prolonged QRS complex duration	Nsun5<tm2b(EUCOMM)Wtsi>/Nsun5<tm2b(EUCOMM)Wtsi>	C57BL/6N-Nsun5<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6408543	F	MP:0020421	increased freezing behavior	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0013510	decreased CD4-negative NK T cell number	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0013691	decreased CD5-positive Ly6C-positive T cell number	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0005387	immune system phenotype	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0013679	increased Ly6C-positive NK T cell number	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0013678	decreased Ly6C-positive NK T cell number	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0013513	decreased memory-marker CD4-negative NK T cell number	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0013772	increased effector memory T-helper cell number	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0000266	abnormal heart morphology	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0000691	enlarged spleen	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0008040	decreased NK T cell number	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0005627	increased circulating potassium level	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0013649	decreased CD11b-high dendritic cell number	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0008725	increased heart atrium size	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0000689	abnormal spleen morphology	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	M	MP:0008045	decreased NK cell number	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408543	F	MP:0001325	abnormal retina morphology	Nub1<tm1b(EUCOMM)Hmgu>/Nub1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nub1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408546	M	MP:0002997	enlarged seminal vesicle	Nwd2<em1(IMPC)Ccpcz>/Nwd2<em1(IMPC)Ccpcz>	C57BL/6N-Nwd2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408546	M	MP:0001262	decreased body weight	Nwd2<em1(IMPC)Ccpcz>/Nwd2<em1(IMPC)Ccpcz>	C57BL/6N-Nwd2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408546	M	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number	Nwd2<em1(IMPC)Ccpcz>/Nwd2<em1(IMPC)Ccpcz>	C57BL/6N-Nwd2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408546	M	MP:0002059	abnormal seminal vesicle morphology	Nwd2<em1(IMPC)Ccpcz>/Nwd2<em1(IMPC)Ccpcz>	C57BL/6N-Nwd2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408547	F	MP:0000598	abnormal liver morphology	Nynrin<em1(IMPC)Mbp>/Nynrin<em1(IMPC)Mbp>	C57BL/6N-Nynrin<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408549	M	MP:0001925	male infertility	Odf1<tm1b(EUCOMM)Hmgu>/Odf1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Odf1<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408549	F	MP:0008810	increased circulating iron level	Odf1<tm1b(EUCOMM)Hmgu>/Odf1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Odf1<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408550	F	MP:0004258	abnormal placenta size	Ola1<em1(IMPC)Bay>/Ola1<em1(IMPC)Bay>	C57BL/6N-Ola1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408552	M	MP:0000443	abnormal snout morphology	P3h2<em1(IMPC)H>/P3h2<+>	C57BL/6N-P3h2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408553	M	MP:0001402	decreased locomotor activity	P3h2<em1(IMPC)H>/P3h2<em1(IMPC)H>	C57BL/6N-P3h2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408553	F	MP:0010088	decreased circulating fructosamine level	P3h2<em1(IMPC)H>/P3h2<em1(IMPC)H>	C57BL/6N-P3h2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408556	F	MP:0002073	abnormal hair growth	Pcdh1<em1(IMPC)Wtsi>/Pcdh1<em1(IMPC)Wtsi>	C57BL/6N-Pcdh1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408557	M	MP:0001410	head bobbing	Pcdh20<em1(IMPC)H>/Pcdh20<em1(IMPC)H>	C57BL/6N-Pcdh20<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408557	F	MP:0020870	decreased thigmotaxis	Pcdh20<em1(IMPC)H>/Pcdh20<em1(IMPC)H>	C57BL/6N-Pcdh20<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408557	F	MP:0001364	decreased anxiety-related response	Pcdh20<em1(IMPC)H>/Pcdh20<em1(IMPC)H>	C57BL/6N-Pcdh20<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408557	F	MP:0004924	abnormal behavior	Pcdh20<em1(IMPC)H>/Pcdh20<em1(IMPC)H>	C57BL/6N-Pcdh20<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408558	F	MP:0002590	increased mean corpuscular volume	Pcsk2<em1(IMPC)H>/Pcsk2<em1(IMPC)H>	C57BL/6NTac-Pcsk2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408558	F	MP:0000367	abnormal coat/ hair morphology	Pcsk2<em1(IMPC)H>/Pcsk2<em1(IMPC)H>	C57BL/6NTac-Pcsk2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408558	F	MP:0001556	increased circulating HDL cholesterol level	Pcsk2<em1(IMPC)H>/Pcsk2<em1(IMPC)H>	C57BL/6NTac-Pcsk2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408558	F	MP:0001513	limb grasping	Pcsk2<em1(IMPC)H>/Pcsk2<em1(IMPC)H>	C57BL/6NTac-Pcsk2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408558	F	MP:0005560	decreased circulating glucose level	Pcsk2<em1(IMPC)H>/Pcsk2<em1(IMPC)H>	C57BL/6NTac-Pcsk2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408558	F	MP:0008810	increased circulating iron level	Pcsk2<em1(IMPC)H>/Pcsk2<em1(IMPC)H>	C57BL/6NTac-Pcsk2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408558	F	MP:0008806	increased circulating amylase level	Pcsk2<em1(IMPC)H>/Pcsk2<em1(IMPC)H>	C57BL/6NTac-Pcsk2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408558	F	MP:0005178	increased circulating cholesterol level	Pcsk2<em1(IMPC)H>/Pcsk2<em1(IMPC)H>	C57BL/6NTac-Pcsk2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408559	M	MP:0002833	increased heart weight	Pde2a<em1(IMPC)H>/Pde2a<+>	C57BL/6NTac-Pde2a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408559	M	MP:0000219	increased neutrophil cell number	Pde2a<em1(IMPC)H>/Pde2a<+>	C57BL/6NTac-Pde2a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408559	F	MP:0005344	increased circulating bilirubin level	Pde2a<em1(IMPC)H>/Pde2a<+>	C57BL/6NTac-Pde2a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408562	F	MP:0001120	abnormal uterus morphology	Pdxdc1<em1(IMPC)Tcp>/Pdxdc1<em1(IMPC)Tcp>	C57BL/6N-Pdxdc1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408562	M	MP:0001157	small seminal vesicle	Pdxdc1<em1(IMPC)Tcp>/Pdxdc1<em1(IMPC)Tcp>	C57BL/6N-Pdxdc1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408562	F	MP:0002060	abnormal skin morphology	Pdxdc1<em1(IMPC)Tcp>/Pdxdc1<em1(IMPC)Tcp>	C57BL/6N-Pdxdc1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408562	M	MP:0001258	decreased body length	Pdxdc1<em1(IMPC)Tcp>/Pdxdc1<em1(IMPC)Tcp>	C57BL/6N-Pdxdc1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408567	F	MP:0001399	hyperactivity	Phf11c<em1(IMPC)Tcp>/Phf11c<em1(IMPC)Tcp>	C57BL/6N-Phf11c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408568	M	MP:0000218	increased leukocyte cell number	Phip<em1(IMPC)Wtsi>/Phip<+>	C57BL/6N-Phip<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408568	F	MP:0001258	decreased body length	Phip<em1(IMPC)Wtsi>/Phip<+>	C57BL/6N-Phip<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408569	F	MP:0002637	small uterus	Phrf1<em1(IMPC)Tcp>/Phrf1<em1(IMPC)Tcp>	C57BL/6N-Phrf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408569	F	MP:0001258	decreased body length	Phrf1<em1(IMPC)Tcp>/Phrf1<em1(IMPC)Tcp>	C57BL/6N-Phrf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408569	F	MP:0000266	abnormal heart morphology	Phrf1<em1(IMPC)Tcp>/Phrf1<em1(IMPC)Tcp>	C57BL/6N-Phrf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408569	F	MP:0003795	abnormal bone structure	Phrf1<em1(IMPC)Tcp>/Phrf1<em1(IMPC)Tcp>	C57BL/6N-Phrf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408569	M	MP:0002059	abnormal seminal vesicle morphology	Phrf1<em1(IMPC)Tcp>/Phrf1<em1(IMPC)Tcp>	C57BL/6N-Phrf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408569	F	MP:0001120	abnormal uterus morphology	Phrf1<em1(IMPC)Tcp>/Phrf1<em1(IMPC)Tcp>	C57BL/6N-Phrf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408569	M	MP:0009516	enlarged salivary gland	Phrf1<em1(IMPC)Tcp>/Phrf1<em1(IMPC)Tcp>	C57BL/6N-Phrf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408569	F	MP:0002135	abnormal kidney morphology	Phrf1<em1(IMPC)Tcp>/Phrf1<em1(IMPC)Tcp>	C57BL/6N-Phrf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408569	M	MP:0000692	small spleen	Phrf1<em1(IMPC)Tcp>/Phrf1<em1(IMPC)Tcp>	C57BL/6N-Phrf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408569	M	MP:0001552	increased circulating triglyceride level	Phrf1<em1(IMPC)Tcp>/Phrf1<em1(IMPC)Tcp>	C57BL/6N-Phrf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408569	F	MP:0002060	abnormal skin morphology	Phrf1<em1(IMPC)Tcp>/Phrf1<em1(IMPC)Tcp>	C57BL/6N-Phrf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408572	F	MP:0000288	abnormal pericardium morphology	Pkdcc<em1(IMPC)Mbp>/Pkdcc<em1(IMPC)Mbp>	C57BL/6N-Pkdcc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408572	F	MP:0003984	embryonic growth retardation	Pkdcc<em1(IMPC)Mbp>/Pkdcc<em1(IMPC)Mbp>	C57BL/6N-Pkdcc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408573	M	MP:0000692	small spleen	Pknox2<em1(IMPC)Ccpcz>/Pknox2<em1(IMPC)Ccpcz>	C57BL/6N-Pknox2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408573	M	MP:0000689	abnormal spleen morphology	Pknox2<em1(IMPC)Ccpcz>/Pknox2<em1(IMPC)Ccpcz>	C57BL/6N-Pknox2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408574	F	MP:0005343	increased circulating aspartate transaminase level	Plag1<em1(IMPC)Hmgu>/Plag1<em1(IMPC)Hmgu>	C57BL/6N-Plag1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408574	M	MP:0010067	increased red blood cell distribution width	Plag1<em1(IMPC)Hmgu>/Plag1<em1(IMPC)Hmgu>	C57BL/6N-Plag1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408574	M	MP:0001258	decreased body length	Plag1<em1(IMPC)Hmgu>/Plag1<em1(IMPC)Hmgu>	C57BL/6N-Plag1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408574	F	MP:0003795	abnormal bone structure	Plag1<em1(IMPC)Hmgu>/Plag1<em1(IMPC)Hmgu>	C57BL/6N-Plag1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408575	M	MP:0001417	decreased exploration in new environment	Plcd4<tm2b(EUCOMM)Hmgu>/Plcd4<tm2b(EUCOMM)Hmgu>	C57BL/6N-Plcd4<tm2b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408576	F	MP:0000691	enlarged spleen	Plce1<em1(IMPC)Mbp>/Plce1<em1(IMPC)Mbp>	C57BL/6N-Plce1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408576	M	MP:0000274	enlarged heart	Plce1<em1(IMPC)Mbp>/Plce1<em1(IMPC)Mbp>	C57BL/6N-Plce1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408576	F	MP:0010392	prolonged QRS complex duration	Plce1<em1(IMPC)Mbp>/Plce1<em1(IMPC)Mbp>	C57BL/6N-Plce1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408576	M	MP:0000266	abnormal heart morphology	Plce1<em1(IMPC)Mbp>/Plce1<em1(IMPC)Mbp>	C57BL/6N-Plce1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408576	M	MP:0002833	increased heart weight	Plce1<em1(IMPC)Mbp>/Plce1<em1(IMPC)Mbp>	C57BL/6N-Plce1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408576	F	MP:0000220	increased monocyte cell number	Plce1<em1(IMPC)Mbp>/Plce1<em1(IMPC)Mbp>	C57BL/6N-Plce1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408576	M	MP:0000219	increased neutrophil cell number	Plce1<em1(IMPC)Mbp>/Plce1<em1(IMPC)Mbp>	C57BL/6N-Plce1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408576	F	MP:0000689	abnormal spleen morphology	Plce1<em1(IMPC)Mbp>/Plce1<em1(IMPC)Mbp>	C57BL/6N-Plce1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408576	M	MP:0005016	decreased lymphocyte cell number	Plce1<em1(IMPC)Mbp>/Plce1<em1(IMPC)Mbp>	C57BL/6N-Plce1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408576	F	MP:0002060	abnormal skin morphology	Plce1<em1(IMPC)Mbp>/Plce1<em1(IMPC)Mbp>	C57BL/6N-Plce1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408577	M	MP:0011896	increased circulating unsaturated transferrin level	Plekha1<tm1b(EUCOMM)Hmgu>/Plekha1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plekha1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408577	M	MP:0001147	small testis	Plekha1<tm1b(EUCOMM)Hmgu>/Plekha1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plekha1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408577	M	MP:0002092	abnormal eye morphology	Plekha1<tm1b(EUCOMM)Hmgu>/Plekha1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plekha1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408578	M	MP:0001944	abnormal pancreas morphology	Poc1b<tm1b(KOMP)Wtsi>/Poc1b<tm1b(KOMP)Wtsi>	C57BL/6N-Poc1b<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6408579	M	MP:0005178	increased circulating cholesterol level	Pon2<tm1b(EUCOMM)Hmgu>/Pon2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pon2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408579	F	MP:0000222	decreased neutrophil cell number	Pon2<tm1b(EUCOMM)Hmgu>/Pon2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pon2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408580	M	MP:0001510	abnormal coat appearance	Ppara<tm1b(EUCOMM)Wtsi>/Ppara<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ppara<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408582	M	MP:0000691	enlarged spleen	Ppm1n<em1(IMPC)Mbp>/Ppm1n<em1(IMPC)Mbp>	C57BL/6N-Ppm1n<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408582	F	MP:0002135	abnormal kidney morphology	Ppm1n<em1(IMPC)Mbp>/Ppm1n<em1(IMPC)Mbp>	C57BL/6N-Ppm1n<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408582	F	MP:0002989	small kidney	Ppm1n<em1(IMPC)Mbp>/Ppm1n<em1(IMPC)Mbp>	C57BL/6N-Ppm1n<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408582	M	MP:0000689	abnormal spleen morphology	Ppm1n<em1(IMPC)Mbp>/Ppm1n<em1(IMPC)Mbp>	C57BL/6N-Ppm1n<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408582	M	MP:0010052	increased grip strength	Ppm1n<em1(IMPC)Mbp>/Ppm1n<em1(IMPC)Mbp>	C57BL/6N-Ppm1n<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408584	M	MP:0013279	increased fasting circulating glucose level	Ppp2r2b<tm1b(KOMP)Wtsi>/Ppp2r2b<tm1b(KOMP)Wtsi>	C57BL/6N-Ppp2r2b<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6408584	F	MP:0005278	abnormal cholesterol homeostasis	Ppp2r2b<tm1b(KOMP)Wtsi>/Ppp2r2b<tm1b(KOMP)Wtsi>	C57BL/6N-Ppp2r2b<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6408584	F	MP:0001325	abnormal retina morphology	Ppp2r2b<tm1b(KOMP)Wtsi>/Ppp2r2b<tm1b(KOMP)Wtsi>	C57BL/6N-Ppp2r2b<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6408586	F	MP:0001469	abnormal contextual conditioning behavior	Ppp4c<em1(IMPC)Ics>/Ppp4c<+>	C57BL/6N-Ppp4c<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408586	M	MP:0002833	increased heart weight	Ppp4c<em1(IMPC)Ics>/Ppp4c<+>	C57BL/6N-Ppp4c<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408587	F	MP:0001126	abnormal ovary morphology	Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ppp4r3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408587	M	MP:0005293	impaired glucose tolerance	Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ppp4r3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408587	M	MP:0000703	abnormal thymus morphology	Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ppp4r3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408587	M	MP:0011964	increased total retina thickness	Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ppp4r3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408587	M	MP:0000598	abnormal liver morphology	Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ppp4r3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408587	M	MP:0002135	abnormal kidney morphology	Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ppp4r3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408587	M	MP:0000691	enlarged spleen	Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ppp4r3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408587	M	MP:0001406	abnormal gait	Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ppp4r3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408587	F	MP:0004906	enlarged uterus	Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ppp4r3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408587	M	MP:0000702	enlarged lymph nodes	Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ppp4r3b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ppp4r3b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408589	F	MP:0001333	absent optic nerve	Prepl<em1(IMPC)H>/Prepl<em1(IMPC)H>	C57BL/6N-Prepl<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408589	M	MP:0001406	abnormal gait	Prepl<em1(IMPC)H>/Prepl<em1(IMPC)H>	C57BL/6N-Prepl<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408590	M	MP:0005016	decreased lymphocyte cell number	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<+>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408590	M	MP:0001148	enlarged testis	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<+>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408590	F	MP:0013675	decreased Ly6C-positive mature NK cell number	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<+>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408590	M	MP:0001146	abnormal testis morphology	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<+>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408591	M	MP:0002941	increased circulating alanine transaminase level	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408591	F	MP:0000689	abnormal spleen morphology	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408591	F	MP:0000691	enlarged spleen	Prkab1<tm1b(KOMP)Wtsi>/Prkab1<tm1b(KOMP)Wtsi>	C57BL/6N-Prkab1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408593	F	MP:0000218	increased leukocyte cell number	Prkd1<em2(IMPC)Wtsi>/Prkd1<+>	C57BL/6N-Prkd1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408593	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Prkd1<em2(IMPC)Wtsi>/Prkd1<+>	C57BL/6N-Prkd1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408593	M	MP:0002079	increased circulating insulin level	Prkd1<em2(IMPC)Wtsi>/Prkd1<+>	C57BL/6N-Prkd1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408593	F	MP:0005561	increased mean corpuscular hemoglobin	Prkd1<em2(IMPC)Wtsi>/Prkd1<+>	C57BL/6N-Prkd1<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408594	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Prkdc<em2(IMPC)Ics>/Prkdc<em2(IMPC)Ics>	C57BL/6N-Prkdc<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408594	F	MP:0001566	increased circulating phosphate level	Prkdc<em2(IMPC)Ics>/Prkdc<em2(IMPC)Ics>	C57BL/6N-Prkdc<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408595	M	MP:0005178	increased circulating cholesterol level	Prkra<em1(IMPC)H>/Prkra<em1(IMPC)H>	C57BL/6N-Prkra<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408595	M	MP:0001925	male infertility	Prkra<em1(IMPC)H>/Prkra<em1(IMPC)H>	C57BL/6N-Prkra<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408596	M	MP:0001146	abnormal testis morphology	Drgx<em1(IMPC)Mbp>/Drgx<+>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408596	M	MP:0002059	abnormal seminal vesicle morphology	Drgx<em1(IMPC)Mbp>/Drgx<+>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408596	F	MP:0001120	abnormal uterus morphology	Drgx<em1(IMPC)Mbp>/Drgx<+>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408596	M	MP:0000598	abnormal liver morphology	Drgx<em1(IMPC)Mbp>/Drgx<+>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408596	F	MP:0000266	abnormal heart morphology	Drgx<em1(IMPC)Mbp>/Drgx<+>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408596	F	MP:0002135	abnormal kidney morphology	Drgx<em1(IMPC)Mbp>/Drgx<+>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408596	F	MP:0000702	enlarged lymph nodes	Drgx<em1(IMPC)Mbp>/Drgx<+>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408596	M	MP:0001148	enlarged testis	Drgx<em1(IMPC)Mbp>/Drgx<+>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408596	F	MP:0002339	abnormal lymph node morphology	Drgx<em1(IMPC)Mbp>/Drgx<+>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408596	F	MP:0000274	enlarged heart	Drgx<em1(IMPC)Mbp>/Drgx<+>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408596	F	MP:0000639	abnormal adrenal gland morphology	Drgx<em1(IMPC)Mbp>/Drgx<+>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408596	F	MP:0002060	abnormal skin morphology	Drgx<em1(IMPC)Mbp>/Drgx<+>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408596	F	MP:0002989	small kidney	Drgx<em1(IMPC)Mbp>/Drgx<+>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408597	M	MP:0003984	embryonic growth retardation	Drgx<em1(IMPC)Mbp>/Drgx<em1(IMPC)Mbp>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408597	F	MP:0011100	preweaning lethality, complete penetrance	Drgx<em1(IMPC)Mbp>/Drgx<em1(IMPC)Mbp>	C57BL/6N-Drgx<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408598	M	MP:0010123	increased bone mineral content	Psd3<em1(IMPC)H>/Psd3<em1(IMPC)H>	C57BL/6N-Psd3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408598	F	MP:0005567	decreased circulating total protein level	Psd3<em1(IMPC)H>/Psd3<em1(IMPC)H>	C57BL/6N-Psd3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408598	M	MP:0010392	prolonged QRS complex duration	Psd3<em1(IMPC)H>/Psd3<em1(IMPC)H>	C57BL/6N-Psd3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408598	M	MP:0003394	increased cardiac output	Psd3<em1(IMPC)H>/Psd3<em1(IMPC)H>	C57BL/6N-Psd3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408598	M	MP:0000062	increased bone mineral density	Psd3<em1(IMPC)H>/Psd3<em1(IMPC)H>	C57BL/6N-Psd3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408598	M	MP:0011951	increased cardiac stroke volume	Psd3<em1(IMPC)H>/Psd3<em1(IMPC)H>	C57BL/6N-Psd3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408598	F	MP:0000745	tremors	Psd3<em1(IMPC)H>/Psd3<em1(IMPC)H>	C57BL/6N-Psd3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408599	M	MP:0013279	increased fasting circulating glucose level	Psg22<em1(IMPC)Wtsi>/Psg22<em1(IMPC)Wtsi>	C57BL/6N-Psg22<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408600	M	MP:0000702	enlarged lymph nodes	Ptp4a2<em1(IMPC)Tcp>/Ptp4a2<em1(IMPC)Tcp>	C57BL/6N-Ptp4a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408600	F	MP:0000470	abnormal stomach morphology	Ptp4a2<em1(IMPC)Tcp>/Ptp4a2<em1(IMPC)Tcp>	C57BL/6N-Ptp4a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408600	M	MP:0010052	increased grip strength	Ptp4a2<em1(IMPC)Tcp>/Ptp4a2<em1(IMPC)Tcp>	C57BL/6N-Ptp4a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408600	F	MP:0002764	short tibia	Ptp4a2<em1(IMPC)Tcp>/Ptp4a2<em1(IMPC)Tcp>	C57BL/6N-Ptp4a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408600	M	MP:0001147	small testis	Ptp4a2<em1(IMPC)Tcp>/Ptp4a2<em1(IMPC)Tcp>	C57BL/6N-Ptp4a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408600	F	MP:0002591	decreased mean corpuscular volume	Ptp4a2<em1(IMPC)Tcp>/Ptp4a2<em1(IMPC)Tcp>	C57BL/6N-Ptp4a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408600	M	MP:0002599	increased mean platelet volume	Ptp4a2<em1(IMPC)Tcp>/Ptp4a2<em1(IMPC)Tcp>	C57BL/6N-Ptp4a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408600	F	MP:0003795	abnormal bone structure	Ptp4a2<em1(IMPC)Tcp>/Ptp4a2<em1(IMPC)Tcp>	C57BL/6N-Ptp4a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408600	M	MP:0001200	thick skin	Ptp4a2<em1(IMPC)Tcp>/Ptp4a2<em1(IMPC)Tcp>	C57BL/6N-Ptp4a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408600	F	MP:0002060	abnormal skin morphology	Ptp4a2<em1(IMPC)Tcp>/Ptp4a2<em1(IMPC)Tcp>	C57BL/6N-Ptp4a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408601	F	MP:0009084	blind uterus	Ptp4a3<em1(IMPC)Mbp>/Ptp4a3<em1(IMPC)Mbp>	C57BL/6N-Ptp4a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408601	M	MP:0000689	abnormal spleen morphology	Ptp4a3<em1(IMPC)Mbp>/Ptp4a3<em1(IMPC)Mbp>	C57BL/6N-Ptp4a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408602	M	MP:0002098	abnormal vibrissa morphology	Rab1a<tm1b(KOMP)Wtsi>/Rab1a<+>	C57BL/6N-Rab1a<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6408604	M	MP:0000692	small spleen	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408604	F	MP:0000691	enlarged spleen	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408604	M	MP:0011874	enlarged urinary bladder	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408604	M	MP:0001147	small testis	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408604	F	MP:0010053	decreased grip strength	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408604	F	MP:0001289	persistence of hyaloid vascular system	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408604	F	MP:0011965	decreased total retina thickness	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408604	F	MP:0001891	hydrocephaly	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408604	M	MP:0005292	improved glucose tolerance	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408604	F	MP:0008528	polycystic kidney	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408604	M	MP:0002792	abnormal retina vasculature morphology	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408604	M	MP:0011886	increased circulating lipase level	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408604	M	MP:0009142	decreased prepulse inhibition	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408604	F	MP:0002764	short tibia	Rabgap1<tm1b(EUCOMM)Hmgu>/Rabgap1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rabgap1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408608	F	MP:0001120	abnormal uterus morphology	Rasgrp3<em1(IMPC)Wtsi>/Rasgrp3<em1(IMPC)Wtsi>	C57BL/6N-Rasgrp3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408608	M	MP:0013436	increased CD8-positive, naive alpha-beta T cell number	Rasgrp3<em1(IMPC)Wtsi>/Rasgrp3<em1(IMPC)Wtsi>	C57BL/6N-Rasgrp3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408608	F	MP:0002092	abnormal eye morphology	Rasgrp3<em1(IMPC)Wtsi>/Rasgrp3<em1(IMPC)Wtsi>	C57BL/6N-Rasgrp3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408608	M	MP:0009453	enhanced contextual conditioning behavior	Rasgrp3<em1(IMPC)Wtsi>/Rasgrp3<em1(IMPC)Wtsi>	C57BL/6N-Rasgrp3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408610	F	MP:0001718	abnormal visceral yolk sac morphology	Rb1cc1<em1(IMPC)Mbp>/Rb1cc1<em1(IMPC)Mbp>	C57BL/6N-Rb1cc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408610	F	MP:0003229	abnormal vitelline vasculature morphology	Rb1cc1<em1(IMPC)Mbp>/Rb1cc1<em1(IMPC)Mbp>	C57BL/6N-Rb1cc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408611	F	MP:0005178	increased circulating cholesterol level	Rbm14<tm1a(KOMP)Wtsi>/Rbm14<tm1a(KOMP)Wtsi>	C57BL/6N-Rbm14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408611	F	MP:0001556	increased circulating HDL cholesterol level	Rbm14<tm1a(KOMP)Wtsi>/Rbm14<tm1a(KOMP)Wtsi>	C57BL/6N-Rbm14<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408613	F	MP:0000702	enlarged lymph nodes	Reln<em1(IMPC)Mbp>/Reln<+>	C57BL/6N-Reln<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408613	M	MP:0002060	abnormal skin morphology	Reln<em1(IMPC)Mbp>/Reln<+>	C57BL/6N-Reln<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408613	F	MP:0000689	abnormal spleen morphology	Reln<em1(IMPC)Mbp>/Reln<+>	C57BL/6N-Reln<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408613	F	MP:0009709	hydrometra	Reln<em1(IMPC)Mbp>/Reln<+>	C57BL/6N-Reln<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408613	F	MP:0001120	abnormal uterus morphology	Reln<em1(IMPC)Mbp>/Reln<+>	C57BL/6N-Reln<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408613	F	MP:0002339	abnormal lymph node morphology	Reln<em1(IMPC)Mbp>/Reln<+>	C57BL/6N-Reln<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408613	F	MP:0000691	enlarged spleen	Reln<em1(IMPC)Mbp>/Reln<+>	C57BL/6N-Reln<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408614	F	MP:0001926	female infertility	Reln<em1(IMPC)Mbp>/Reln<em1(IMPC)Mbp>	C57BL/6N-Reln<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408614	M	MP:0001925	male infertility	Reln<em1(IMPC)Mbp>/Reln<em1(IMPC)Mbp>	C57BL/6N-Reln<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408615	M	MP:0000266	abnormal heart morphology	Retreg2<em2(IMPC)Ccpcz>/Retreg2<em2(IMPC)Ccpcz>	C57BL/6N-Retreg2<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408615	F	MP:0000689	abnormal spleen morphology	Retreg2<em2(IMPC)Ccpcz>/Retreg2<em2(IMPC)Ccpcz>	C57BL/6N-Retreg2<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408615	M	MP:0020421	increased freezing behavior	Retreg2<em2(IMPC)Ccpcz>/Retreg2<em2(IMPC)Ccpcz>	C57BL/6N-Retreg2<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408615	F	MP:0000691	enlarged spleen	Retreg2<em2(IMPC)Ccpcz>/Retreg2<em2(IMPC)Ccpcz>	C57BL/6N-Retreg2<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408616	M	MP:0010067	increased red blood cell distribution width	Rgl1<em1(IMPC)Mbp>/Rgl1<+>	C57BL/6N-Rgl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408616	F	MP:0001711	abnormal placenta morphology	Rgl1<em1(IMPC)Mbp>/Rgl1<+>	C57BL/6N-Rgl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408616	M	MP:0001488	increased startle reflex	Rgl1<em1(IMPC)Mbp>/Rgl1<+>	C57BL/6N-Rgl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408616	M	MP:0003068	enlarged kidney	Rgl1<em1(IMPC)Mbp>/Rgl1<+>	C57BL/6N-Rgl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408616	F	MP:0000274	enlarged heart	Rgl1<em1(IMPC)Mbp>/Rgl1<+>	C57BL/6N-Rgl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408616	F	MP:0000266	abnormal heart morphology	Rgl1<em1(IMPC)Mbp>/Rgl1<+>	C57BL/6N-Rgl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408616	M	MP:0000219	increased neutrophil cell number	Rgl1<em1(IMPC)Mbp>/Rgl1<+>	C57BL/6N-Rgl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408616	M	MP:0002135	abnormal kidney morphology	Rgl1<em1(IMPC)Mbp>/Rgl1<+>	C57BL/6N-Rgl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408617	F	MP:0006108	abnormal hindbrain development	Rgl1<em1(IMPC)Mbp>/Rgl1<em1(IMPC)Mbp>	C57BL/6N-Rgl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408619	M	MP:0000691	enlarged spleen	Rgs2<em1(IMPC)H>/Rgs2<em1(IMPC)H>	C57BL/6NTac-Rgs2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408619	F	MP:0001314	cornea opacity	Rgs2<em1(IMPC)H>/Rgs2<em1(IMPC)H>	C57BL/6NTac-Rgs2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408619	F	MP:0020421	increased freezing behavior	Rgs2<em1(IMPC)H>/Rgs2<em1(IMPC)H>	C57BL/6NTac-Rgs2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408619	F	MP:0005553	increased circulating creatinine level	Rgs2<em1(IMPC)H>/Rgs2<em1(IMPC)H>	C57BL/6NTac-Rgs2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408619	F	MP:0013278	decreased fasting circulating glucose level	Rgs2<em1(IMPC)H>/Rgs2<em1(IMPC)H>	C57BL/6NTac-Rgs2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408620	M	MP:0013679	increased Ly6C-positive NK T cell number	Rhobtb1<em2(IMPC)Ccpcz>/Rhobtb1<em2(IMPC)Ccpcz>	C57BL/6N-Rhobtb1<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408620	M	MP:0005355	enlarged thyroid gland	Rhobtb1<em2(IMPC)Ccpcz>/Rhobtb1<em2(IMPC)Ccpcz>	C57BL/6N-Rhobtb1<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408620	M	MP:0000681	abnormal thyroid gland morphology	Rhobtb1<em2(IMPC)Ccpcz>/Rhobtb1<em2(IMPC)Ccpcz>	C57BL/6N-Rhobtb1<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408621	M	MP:0002075	abnormal coat/hair pigmentation	Rnf168<em1(IMPC)H>/Rnf168<em1(IMPC)H>	C57BL/6NTac-Rnf168<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408621	F	MP:0002941	increased circulating alanine transaminase level	Rnf168<em1(IMPC)H>/Rnf168<em1(IMPC)H>	C57BL/6NTac-Rnf168<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408621	F	MP:0010090	increased circulating creatine kinase level	Rnf168<em1(IMPC)H>/Rnf168<em1(IMPC)H>	C57BL/6NTac-Rnf168<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408622	M	MP:0000266	abnormal heart morphology	Rnf19b<em1(IMPC)Ccpcz>/Rnf19b<+>	C57BL/6N-Rnf19b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408622	M	MP:0003179	thrombocytopenia	Rnf19b<em1(IMPC)Ccpcz>/Rnf19b<+>	C57BL/6N-Rnf19b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408622	M	MP:0000274	enlarged heart	Rnf19b<em1(IMPC)Ccpcz>/Rnf19b<+>	C57BL/6N-Rnf19b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408622	M	MP:0005011	increased eosinophil cell number	Rnf19b<em1(IMPC)Ccpcz>/Rnf19b<+>	C57BL/6N-Rnf19b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408623	M	MP:0001925	male infertility	Rnf41<em1(IMPC)Bay>/Rnf41<em1(IMPC)Bay>	C57BL/6N-Rnf41<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408623	M	MP:0001488	increased startle reflex	Rnf41<em1(IMPC)Bay>/Rnf41<em1(IMPC)Bay>	C57BL/6N-Rnf41<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408624	M	MP:0005568	increased circulating total protein level	Rnf4<em1(IMPC)Ccpcz>/Rnf4<+>	C57BL/6N-Rnf4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408624	M	MP:0001552	increased circulating triglyceride level	Rnf4<em1(IMPC)Ccpcz>/Rnf4<+>	C57BL/6N-Rnf4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408624	M	MP:0001147	small testis	Rnf4<em1(IMPC)Ccpcz>/Rnf4<+>	C57BL/6N-Rnf4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408624	M	MP:0001146	abnormal testis morphology	Rnf4<em1(IMPC)Ccpcz>/Rnf4<+>	C57BL/6N-Rnf4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408625	F	MP:0005084	abnormal gallbladder morphology	Rnf5<tm1.1(KOMP)Vlcg>/Rnf5<+>	C57BL/6N-Rnf5<tm1.1(KOMP)Vlcg>/Ccpcz	N	MGI:5576271
MGI:6408625	F	MP:0000703	abnormal thymus morphology	Rnf5<tm1.1(KOMP)Vlcg>/Rnf5<+>	C57BL/6N-Rnf5<tm1.1(KOMP)Vlcg>/Ccpcz	N	MGI:5576271
MGI:6408625	M	MP:0002060	abnormal skin morphology	Rnf5<tm1.1(KOMP)Vlcg>/Rnf5<+>	C57BL/6N-Rnf5<tm1.1(KOMP)Vlcg>/Ccpcz	N	MGI:5576271
MGI:6408625	F	MP:0000709	enlarged thymus	Rnf5<tm1.1(KOMP)Vlcg>/Rnf5<+>	C57BL/6N-Rnf5<tm1.1(KOMP)Vlcg>/Ccpcz	N	MGI:5576271
MGI:6408625	F	MP:0009342	enlarged gallbladder	Rnf5<tm1.1(KOMP)Vlcg>/Rnf5<+>	C57BL/6N-Rnf5<tm1.1(KOMP)Vlcg>/Ccpcz	N	MGI:5576271
MGI:6408626	F	MP:0002060	abnormal skin morphology	Rnf5<tm1.1(KOMP)Vlcg>/Rnf5<tm1.1(KOMP)Vlcg>	C57BL/6N-Rnf5<tm1.1(KOMP)Vlcg>/Ccpcz	N	MGI:5576271
MGI:6408626	F	MP:0000689	abnormal spleen morphology	Rnf5<tm1.1(KOMP)Vlcg>/Rnf5<tm1.1(KOMP)Vlcg>	C57BL/6N-Rnf5<tm1.1(KOMP)Vlcg>/Ccpcz	N	MGI:5576271
MGI:6408627	M	MP:0000627	abnormal mammary gland morphology	Rnft1<em1(IMPC)Ccpcz>/Rnft1<em1(IMPC)Ccpcz>	C57BL/6N-Rnft1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408627	M	MP:0002135	abnormal kidney morphology	Rnft1<em1(IMPC)Ccpcz>/Rnft1<em1(IMPC)Ccpcz>	C57BL/6N-Rnft1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408627	M	MP:0003917	increased kidney weight	Rnft1<em1(IMPC)Ccpcz>/Rnft1<em1(IMPC)Ccpcz>	C57BL/6N-Rnft1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408628	F	MP:0011100	preweaning lethality, complete penetrance	Robo1<em1(IMPC)Mbp>/Robo1<em1(IMPC)Mbp>	C57BL/6N-Robo1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408629	M	MP:0002135	abnormal kidney morphology	Robo2<em1(IMPC)Mbp>/Robo2<+>	C57BL/6N-Robo2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408629	M	MP:0003068	enlarged kidney	Robo2<em1(IMPC)Mbp>/Robo2<+>	C57BL/6N-Robo2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408632	F	MP:0000195	decreased circulating calcium level	Rras<em1(IMPC)H>/Rras<em1(IMPC)H>	C57BL/6N-Rras<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408632	M	MP:0013278	decreased fasting circulating glucose level	Rras<em1(IMPC)H>/Rras<em1(IMPC)H>	C57BL/6N-Rras<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408632	M	MP:0002965	increased circulating serum albumin level	Rras<em1(IMPC)H>/Rras<em1(IMPC)H>	C57BL/6N-Rras<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408632	M	MP:0001552	increased circulating triglyceride level	Rras<em1(IMPC)H>/Rras<em1(IMPC)H>	C57BL/6N-Rras<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408634	F	MP:0001552	increased circulating triglyceride level	Runx1t1<tm1b(EUCOMM)Hmgu>/Runx1t1<+>	C57BL/6N-Runx1t1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408637	F	MP:0001399	hyperactivity	Sbspon<em1(IMPC)Ccpcz>/Sbspon<em1(IMPC)Ccpcz>	C57BL/6N-Sbspon<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408637	F	MP:0001402	decreased locomotor activity	Sbspon<em1(IMPC)Ccpcz>/Sbspon<em1(IMPC)Ccpcz>	C57BL/6N-Sbspon<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408637	F	MP:0004924	abnormal behavior	Sbspon<em1(IMPC)Ccpcz>/Sbspon<em1(IMPC)Ccpcz>	C57BL/6N-Sbspon<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408637	M	MP:0001146	abnormal testis morphology	Sbspon<em1(IMPC)Ccpcz>/Sbspon<em1(IMPC)Ccpcz>	C57BL/6N-Sbspon<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408637	F	MP:0020870	decreased thigmotaxis	Sbspon<em1(IMPC)Ccpcz>/Sbspon<em1(IMPC)Ccpcz>	C57BL/6N-Sbspon<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408637	M	MP:0000627	abnormal mammary gland morphology	Sbspon<em1(IMPC)Ccpcz>/Sbspon<em1(IMPC)Ccpcz>	C57BL/6N-Sbspon<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408637	M	MP:0001147	small testis	Sbspon<em1(IMPC)Ccpcz>/Sbspon<em1(IMPC)Ccpcz>	C57BL/6N-Sbspon<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408638	M	MP:0009476	enlarged cecum	Scmh1<tm1e.1(EUCOMM)Hmgu>/Scmh1<tm1e.1(EUCOMM)Hmgu>	C57BL/6N-Scmh1<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408638	M	MP:0000598	abnormal liver morphology	Scmh1<tm1e.1(EUCOMM)Hmgu>/Scmh1<tm1e.1(EUCOMM)Hmgu>	C57BL/6N-Scmh1<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408641	F	MP:0010579	increased heart left ventricle size	Scn2b<em1(IMPC)Bay>/Scn2b<em1(IMPC)Bay>	C57BL/6N-Scn2b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408643	M	MP:0010124	decreased bone mineral content	Sdc3<em1(IMPC)Wtsi>/Sdc3<em1(IMPC)Wtsi>	C57BL/6N-Sdc3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408643	M	MP:0002073	abnormal hair growth	Sdc3<em1(IMPC)Wtsi>/Sdc3<em1(IMPC)Wtsi>	C57BL/6N-Sdc3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408646	F	MP:0001697	abnormal embryo size	Septin11<em1(IMPC)Tcp>/Septin11<em1(IMPC)Tcp>	C57BL/6N-Septin11<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408646	F	MP:0003984	embryonic growth retardation	Septin11<em1(IMPC)Tcp>/Septin11<em1(IMPC)Tcp>	C57BL/6N-Septin11<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408647	M	MP:0008805	decreased circulating amylase level	Sfpq<tm1a(EUCOMM)Wtsi>/Sfpq<+>	C57BL/6N-Sfpq<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408648	F	MP:0005011	increased eosinophil cell number	Sgce<em1(IMPC)H>/Sgce<em1(IMPC)H>	C57BL/6N-Sgce<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408650	F	MP:0000195	decreased circulating calcium level	Shank3<em1(IMPC)H>/Shank3<em1(IMPC)H>	C57BL/6NTac-Shank3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408651	M	MP:0002059	abnormal seminal vesicle morphology	Shisa6<em1(IMPC)Tcp>/Shisa6<em1(IMPC)Tcp>	C57BL/6N-Shisa6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408651	M	MP:0000219	increased neutrophil cell number	Shisa6<em1(IMPC)Tcp>/Shisa6<em1(IMPC)Tcp>	C57BL/6N-Shisa6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408651	M	MP:0000221	decreased leukocyte cell number	Shisa6<em1(IMPC)Tcp>/Shisa6<em1(IMPC)Tcp>	C57BL/6N-Shisa6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408651	M	MP:0002833	increased heart weight	Shisa6<em1(IMPC)Tcp>/Shisa6<em1(IMPC)Tcp>	C57BL/6N-Shisa6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408651	M	MP:0005016	decreased lymphocyte cell number	Shisa6<em1(IMPC)Tcp>/Shisa6<em1(IMPC)Tcp>	C57BL/6N-Shisa6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408652	M	MP:0009142	decreased prepulse inhibition	Shisa9<em1(IMPC)H>/Shisa9<em1(IMPC)H>	C57BL/6N-Shisa9<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408653	F	MP:0013279	increased fasting circulating glucose level	Shisal1<em1(IMPC)Ccpcz>/Shisal1<em1(IMPC)Ccpcz>	C57BL/6N-Shisal1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408653	F	MP:0002092	abnormal eye morphology	Shisal1<em1(IMPC)Ccpcz>/Shisal1<em1(IMPC)Ccpcz>	C57BL/6N-Shisal1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408653	F	MP:0009342	enlarged gallbladder	Shisal1<em1(IMPC)Ccpcz>/Shisal1<em1(IMPC)Ccpcz>	C57BL/6N-Shisal1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408653	F	MP:0020421	increased freezing behavior	Shisal1<em1(IMPC)Ccpcz>/Shisal1<em1(IMPC)Ccpcz>	C57BL/6N-Shisal1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408653	F	MP:0005084	abnormal gallbladder morphology	Shisal1<em1(IMPC)Ccpcz>/Shisal1<em1(IMPC)Ccpcz>	C57BL/6N-Shisal1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408653	F	MP:0000709	enlarged thymus	Shisal1<em1(IMPC)Ccpcz>/Shisal1<em1(IMPC)Ccpcz>	C57BL/6N-Shisal1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408653	F	MP:0000703	abnormal thymus morphology	Shisal1<em1(IMPC)Ccpcz>/Shisal1<em1(IMPC)Ccpcz>	C57BL/6N-Shisal1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408653	F	MP:0002060	abnormal skin morphology	Shisal1<em1(IMPC)Ccpcz>/Shisal1<em1(IMPC)Ccpcz>	C57BL/6N-Shisal1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408653	F	MP:0002135	abnormal kidney morphology	Shisal1<em1(IMPC)Ccpcz>/Shisal1<em1(IMPC)Ccpcz>	C57BL/6N-Shisal1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408653	M	MP:0010097	abnormal retina blood vessel morphology	Shisal1<em1(IMPC)Ccpcz>/Shisal1<em1(IMPC)Ccpcz>	C57BL/6N-Shisal1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408654	M	MP:0001147	small testis	Sinhcaf<em1(IMPC)Ccpcz>/Sinhcaf<+>	C57BL/6N-Sinhcaf<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408654	M	MP:0003068	enlarged kidney	Sinhcaf<em1(IMPC)Ccpcz>/Sinhcaf<+>	C57BL/6N-Sinhcaf<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408654	M	MP:0001146	abnormal testis morphology	Sinhcaf<em1(IMPC)Ccpcz>/Sinhcaf<+>	C57BL/6N-Sinhcaf<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408654	M	MP:0002135	abnormal kidney morphology	Sinhcaf<em1(IMPC)Ccpcz>/Sinhcaf<+>	C57BL/6N-Sinhcaf<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408655	F	MP:0001410	head bobbing	Sipa1<tm1b(EUCOMM)Hmgu>/Sipa1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sipa1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408657	M	MP:0003231	abnormal placenta vasculature	Slc12a5<em1(IMPC)Mbp>/Slc12a5<em1(IMPC)Mbp>	C57BL/6N-Slc12a5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408659	M	MP:0002339	abnormal lymph node morphology	Slc17a8<em1(IMPC)Mbp>/Slc17a8<em1(IMPC)Mbp>	C57BL/6N-Slc17a8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408659	F	MP:0000639	abnormal adrenal gland morphology	Slc17a8<em1(IMPC)Mbp>/Slc17a8<em1(IMPC)Mbp>	C57BL/6N-Slc17a8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408659	F	MP:0002092	abnormal eye morphology	Slc17a8<em1(IMPC)Mbp>/Slc17a8<em1(IMPC)Mbp>	C57BL/6N-Slc17a8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408659	M	MP:0000702	enlarged lymph nodes	Slc17a8<em1(IMPC)Mbp>/Slc17a8<em1(IMPC)Mbp>	C57BL/6N-Slc17a8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408659	M	MP:0001304	cataract	Slc17a8<em1(IMPC)Mbp>/Slc17a8<em1(IMPC)Mbp>	C57BL/6N-Slc17a8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408659	F	MP:0001120	abnormal uterus morphology	Slc17a8<em1(IMPC)Mbp>/Slc17a8<em1(IMPC)Mbp>	C57BL/6N-Slc17a8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408659	M	MP:0000495	abnormal colon morphology	Slc17a8<em1(IMPC)Mbp>/Slc17a8<em1(IMPC)Mbp>	C57BL/6N-Slc17a8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408659	M	MP:0002135	abnormal kidney morphology	Slc17a8<em1(IMPC)Mbp>/Slc17a8<em1(IMPC)Mbp>	C57BL/6N-Slc17a8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408659	F	MP:0004906	enlarged uterus	Slc17a8<em1(IMPC)Mbp>/Slc17a8<em1(IMPC)Mbp>	C57BL/6N-Slc17a8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408659	M	MP:0001417	decreased exploration in new environment	Slc17a8<em1(IMPC)Mbp>/Slc17a8<em1(IMPC)Mbp>	C57BL/6N-Slc17a8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408660	F	MP:0000691	enlarged spleen	Slc26a9<em1(IMPC)Mbp>/Slc26a9<+>	C57BL/6N-Slc26a9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408660	M	MP:0003068	enlarged kidney	Slc26a9<em1(IMPC)Mbp>/Slc26a9<+>	C57BL/6N-Slc26a9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408660	M	MP:0002135	abnormal kidney morphology	Slc26a9<em1(IMPC)Mbp>/Slc26a9<+>	C57BL/6N-Slc26a9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408660	F	MP:0001314	cornea opacity	Slc26a9<em1(IMPC)Mbp>/Slc26a9<+>	C57BL/6N-Slc26a9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408660	F	MP:0000689	abnormal spleen morphology	Slc26a9<em1(IMPC)Mbp>/Slc26a9<+>	C57BL/6N-Slc26a9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408661	M	MP:0001614	abnormal blood vessel morphology	Slc26a9<em1(IMPC)Mbp>/Slc26a9<em1(IMPC)Mbp>	C57BL/6N-Slc26a9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408661	M	MP:0001914	hemorrhage	Slc26a9<em1(IMPC)Mbp>/Slc26a9<em1(IMPC)Mbp>	C57BL/6N-Slc26a9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408662	F	MP:0005108	abnormal ulna morphology	Slc29a4<tm1b(KOMP)Wtsi>/Slc29a4<tm1b(KOMP)Wtsi>	C57BL/6N-Slc29a4<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408662	F	MP:0000552	abnormal radius morphology	Slc29a4<tm1b(KOMP)Wtsi>/Slc29a4<tm1b(KOMP)Wtsi>	C57BL/6N-Slc29a4<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408664	F	MP:0013279	increased fasting circulating glucose level	Slc50a1<tm1.1(KOMP)Vlcg>/Slc50a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc50a1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6408664	F	MP:0002941	increased circulating alanine transaminase level	Slc50a1<tm1.1(KOMP)Vlcg>/Slc50a1<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc50a1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6408665	F	MP:0000702	enlarged lymph nodes	Slc6a6<em1(IMPC)Mbp>/Slc6a6<em1(IMPC)Mbp>	C57BL/6N-Slc6a6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408665	F	MP:0002339	abnormal lymph node morphology	Slc6a6<em1(IMPC)Mbp>/Slc6a6<em1(IMPC)Mbp>	C57BL/6N-Slc6a6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408665	M	MP:0002875	decreased erythrocyte cell number	Slc6a6<em1(IMPC)Mbp>/Slc6a6<em1(IMPC)Mbp>	C57BL/6N-Slc6a6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408665	M	MP:0006243	impaired pupillary reflex	Slc6a6<em1(IMPC)Mbp>/Slc6a6<em1(IMPC)Mbp>	C57BL/6N-Slc6a6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408665	F	MP:0001399	hyperactivity	Slc6a6<em1(IMPC)Mbp>/Slc6a6<em1(IMPC)Mbp>	C57BL/6N-Slc6a6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408667	F	MP:0005565	increased blood urea nitrogen level	Slc7a2<tm1b(EUCOMM)Hmgu>/Slc7a2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc7a2<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408667	F	MP:0004357	long tibia	Slc7a2<tm1b(EUCOMM)Hmgu>/Slc7a2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc7a2<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408667	F	MP:0008810	increased circulating iron level	Slc7a2<tm1b(EUCOMM)Hmgu>/Slc7a2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Slc7a2<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408668	M	MP:0001925	male infertility	Slc9a1<em1(IMPC)Mbp>/Slc9a1<em1(IMPC)Mbp>	C57BL/6N-Slc9a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408669	F	MP:0002874	decreased hemoglobin content	Nherf2<tm2a(EUCOMM)Hmgu>/Nherf2<tm2a(EUCOMM)Hmgu>	C57BL/6N-Nherf2<tm2a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6408669	F	MP:0000208	decreased hematocrit	Nherf2<tm2a(EUCOMM)Hmgu>/Nherf2<tm2a(EUCOMM)Hmgu>	C57BL/6N-Nherf2<tm2a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6408669	F	MP:0002968	increased circulating alkaline phosphatase level	Nherf2<tm2a(EUCOMM)Hmgu>/Nherf2<tm2a(EUCOMM)Hmgu>	C57BL/6N-Nherf2<tm2a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6408670	M	MP:0002968	increased circulating alkaline phosphatase level	Slx1b<em1(IMPC)Ics>/Slx1b<+>	C57BL/6N-Slx1b<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408671	M	MP:0001304	cataract	Spata24<tm1b(EUCOMM)Wtsi>/Spata24<tm1b(EUCOMM)Wtsi>	C57BL/6N-Spata24<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408671	M	MP:0002953	thick ventricular wall	Spata24<tm1b(EUCOMM)Wtsi>/Spata24<tm1b(EUCOMM)Wtsi>	C57BL/6N-Spata24<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408671	M	MP:0000222	decreased neutrophil cell number	Spata24<tm1b(EUCOMM)Wtsi>/Spata24<tm1b(EUCOMM)Wtsi>	C57BL/6N-Spata24<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408672	M	MP:0013676	increased Ly6C-positive mature NK cell number	Spink6<em1(IMPC)Ccpcz>/Spink6<em1(IMPC)Ccpcz>	C57BL/6N-Spink6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408672	M	MP:0003884	decreased macrophage cell number	Spink6<em1(IMPC)Ccpcz>/Spink6<em1(IMPC)Ccpcz>	C57BL/6N-Spink6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408672	M	MP:0000220	increased monocyte cell number	Spink6<em1(IMPC)Ccpcz>/Spink6<em1(IMPC)Ccpcz>	C57BL/6N-Spink6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408674	F	MP:0001392	abnormal locomotor behavior	Spn<em1(IMPC)Ics>/Spn<em1(IMPC)Ics>	C57BL/6N-Spn<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408674	M	MP:0010024	increased total body fat amount	Spn<em1(IMPC)Ics>/Spn<em1(IMPC)Ics>	C57BL/6N-Spn<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408674	F	MP:0004357	long tibia	Spn<em1(IMPC)Ics>/Spn<em1(IMPC)Ics>	C57BL/6N-Spn<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408674	M	MP:0003961	decreased lean body mass	Spn<em1(IMPC)Ics>/Spn<em1(IMPC)Ics>	C57BL/6N-Spn<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408674	F	MP:0001257	increased body length	Spn<em1(IMPC)Ics>/Spn<em1(IMPC)Ics>	C57BL/6N-Spn<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408674	F	MP:0020420	abnormal freezing behavior	Spn<em1(IMPC)Ics>/Spn<em1(IMPC)Ics>	C57BL/6N-Spn<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408674	M	MP:0011962	increased cornea thickness	Spn<em1(IMPC)Ics>/Spn<em1(IMPC)Ics>	C57BL/6N-Spn<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6408675	F	MP:0002764	short tibia	Spry4<tm1b(KOMP)Mbp>/Spry4<tm1b(KOMP)Mbp>	C57BL/6N-Spry4<tm1b(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:6408675	M	MP:0001399	hyperactivity	Spry4<tm1b(KOMP)Mbp>/Spry4<tm1b(KOMP)Mbp>	C57BL/6N-Spry4<tm1b(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:6408676	M	MP:0001488	increased startle reflex	Spta1<em1(IMPC)Bay>/Spta1<+>	C57BL/6N-Spta1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6408679	F	MP:0003179	thrombocytopenia	Srcap<em1(IMPC)Wtsi>/Srcap<+>	C57BL/6N-Srcap<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408679	F	MP:0002073	abnormal hair growth	Srcap<em1(IMPC)Wtsi>/Srcap<+>	C57BL/6N-Srcap<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408680	F	MP:0009084	blind uterus	Sstr2<em1(IMPC)Mbp>/Sstr2<em1(IMPC)Mbp>	C57BL/6N-Sstr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408680	F	MP:0000274	enlarged heart	Sstr2<em1(IMPC)Mbp>/Sstr2<em1(IMPC)Mbp>	C57BL/6N-Sstr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408680	F	MP:0000692	small spleen	Sstr2<em1(IMPC)Mbp>/Sstr2<em1(IMPC)Mbp>	C57BL/6N-Sstr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408680	F	MP:0000266	abnormal heart morphology	Sstr2<em1(IMPC)Mbp>/Sstr2<em1(IMPC)Mbp>	C57BL/6N-Sstr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408680	F	MP:0002135	abnormal kidney morphology	Sstr2<em1(IMPC)Mbp>/Sstr2<em1(IMPC)Mbp>	C57BL/6N-Sstr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408680	M	MP:0001200	thick skin	Sstr2<em1(IMPC)Mbp>/Sstr2<em1(IMPC)Mbp>	C57BL/6N-Sstr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408680	F	MP:0002092	abnormal eye morphology	Sstr2<em1(IMPC)Mbp>/Sstr2<em1(IMPC)Mbp>	C57BL/6N-Sstr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408683	F	MP:0002135	abnormal kidney morphology	Stim1<em1(IMPC)Mbp>/Stim1<+>	C57BL/6N-Stim1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408683	F	MP:0005013	increased lymphocyte cell number	Stim1<em1(IMPC)Mbp>/Stim1<+>	C57BL/6N-Stim1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408683	M	MP:0003068	enlarged kidney	Stim1<em1(IMPC)Mbp>/Stim1<+>	C57BL/6N-Stim1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408683	F	MP:0000219	increased neutrophil cell number	Stim1<em1(IMPC)Mbp>/Stim1<+>	C57BL/6N-Stim1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408683	M	MP:0000274	enlarged heart	Stim1<em1(IMPC)Mbp>/Stim1<+>	C57BL/6N-Stim1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408683	F	MP:0000218	increased leukocyte cell number	Stim1<em1(IMPC)Mbp>/Stim1<+>	C57BL/6N-Stim1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408683	F	MP:0002060	abnormal skin morphology	Stim1<em1(IMPC)Mbp>/Stim1<+>	C57BL/6N-Stim1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408683	F	MP:0002092	abnormal eye morphology	Stim1<em1(IMPC)Mbp>/Stim1<+>	C57BL/6N-Stim1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408683	F	MP:0000702	enlarged lymph nodes	Stim1<em1(IMPC)Mbp>/Stim1<+>	C57BL/6N-Stim1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408683	F	MP:0002989	small kidney	Stim1<em1(IMPC)Mbp>/Stim1<+>	C57BL/6N-Stim1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408683	F	MP:0001417	decreased exploration in new environment	Stim1<em1(IMPC)Mbp>/Stim1<+>	C57BL/6N-Stim1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408683	F	MP:0002339	abnormal lymph node morphology	Stim1<em1(IMPC)Mbp>/Stim1<+>	C57BL/6N-Stim1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408685	M	MP:0001944	abnormal pancreas morphology	Stk26<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Stk26<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408685	M	MP:0008935	decreased mean platelet volume	Stk26<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Stk26<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408685	M	MP:0005355	enlarged thyroid gland	Stk26<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Stk26<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408685	M	MP:0000681	abnormal thyroid gland morphology	Stk26<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Stk26<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408685	M	MP:0008039	increased NK T cell number	Stk26<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Stk26<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408685	M	MP:0003450	enlarged pancreas	Stk26<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Stk26<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408686	F	MP:0005554	decreased circulating creatinine level	Stk26<tm1b(EUCOMM)Hmgu>/Stk26<tm1b(EUCOMM)Hmgu>	C57BL/6N-Stk26<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408686	F	MP:0004599	abnormal vertebral arch morphology	Stk26<tm1b(EUCOMM)Hmgu>/Stk26<tm1b(EUCOMM)Hmgu>	C57BL/6N-Stk26<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408686	F	MP:0000639	abnormal adrenal gland morphology	Stk26<tm1b(EUCOMM)Hmgu>/Stk26<tm1b(EUCOMM)Hmgu>	C57BL/6N-Stk26<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408686	F	MP:0002135	abnormal kidney morphology	Stk26<tm1b(EUCOMM)Hmgu>/Stk26<tm1b(EUCOMM)Hmgu>	C57BL/6N-Stk26<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408686	F	MP:0000642	enlarged adrenal glands	Stk26<tm1b(EUCOMM)Hmgu>/Stk26<tm1b(EUCOMM)Hmgu>	C57BL/6N-Stk26<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408686	F	MP:0008935	decreased mean platelet volume	Stk26<tm1b(EUCOMM)Hmgu>/Stk26<tm1b(EUCOMM)Hmgu>	C57BL/6N-Stk26<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408686	F	MP:0000223	decreased monocyte cell number	Stk26<tm1b(EUCOMM)Hmgu>/Stk26<tm1b(EUCOMM)Hmgu>	C57BL/6N-Stk26<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408688	F	MP:0005343	increased circulating aspartate transaminase level	Stoml2<tm1(KOMP)Vlcg>/Stoml2<tm1(KOMP)Vlcg>	C57BL/6N-Stoml2<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408688	M	MP:0002079	increased circulating insulin level	Stoml2<tm1(KOMP)Vlcg>/Stoml2<tm1(KOMP)Vlcg>	C57BL/6N-Stoml2<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408688	F	MP:0002941	increased circulating alanine transaminase level	Stoml2<tm1(KOMP)Vlcg>/Stoml2<tm1(KOMP)Vlcg>	C57BL/6N-Stoml2<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408688	M	MP:0001925	male infertility	Stoml2<tm1(KOMP)Vlcg>/Stoml2<tm1(KOMP)Vlcg>	C57BL/6N-Stoml2<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408688	F	MP:0005344	increased circulating bilirubin level	Stoml2<tm1(KOMP)Vlcg>/Stoml2<tm1(KOMP)Vlcg>	C57BL/6N-Stoml2<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408689	M	MP:0002059	abnormal seminal vesicle morphology	Strip2<em1(IMPC)Ccpcz>/Strip2<em1(IMPC)Ccpcz>	C57BL/6N-Strip2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408689	M	MP:0003450	enlarged pancreas	Strip2<em1(IMPC)Ccpcz>/Strip2<em1(IMPC)Ccpcz>	C57BL/6N-Strip2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408689	M	MP:0001944	abnormal pancreas morphology	Strip2<em1(IMPC)Ccpcz>/Strip2<em1(IMPC)Ccpcz>	C57BL/6N-Strip2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408691	M	MP:0002968	increased circulating alkaline phosphatase level	Stx6<em1(IMPC)H>/Stx6<em1(IMPC)H>	C57BL/6NTac-Stx6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408691	M	MP:0002098	abnormal vibrissa morphology	Stx6<em1(IMPC)H>/Stx6<em1(IMPC)H>	C57BL/6NTac-Stx6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408691	M	MP:0005178	increased circulating cholesterol level	Stx6<em1(IMPC)H>/Stx6<em1(IMPC)H>	C57BL/6NTac-Stx6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408691	F	MP:0001364	decreased anxiety-related response	Stx6<em1(IMPC)H>/Stx6<em1(IMPC)H>	C57BL/6NTac-Stx6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408691	M	MP:0005560	decreased circulating glucose level	Stx6<em1(IMPC)H>/Stx6<em1(IMPC)H>	C57BL/6NTac-Stx6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408691	F	MP:0005565	increased blood urea nitrogen level	Stx6<em1(IMPC)H>/Stx6<em1(IMPC)H>	C57BL/6NTac-Stx6<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408693	M	MP:0001147	small testis	Syce2<em1(IMPC)Tcp>/Syce2<em1(IMPC)Tcp>	C57BL/6N-Syce2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408693	F	MP:0003961	decreased lean body mass	Syce2<em1(IMPC)Tcp>/Syce2<em1(IMPC)Tcp>	C57BL/6N-Syce2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408693	M	MP:0004930	small epididymis	Syce2<em1(IMPC)Tcp>/Syce2<em1(IMPC)Tcp>	C57BL/6N-Syce2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408693	M	MP:0001925	male infertility	Syce2<em1(IMPC)Tcp>/Syce2<em1(IMPC)Tcp>	C57BL/6N-Syce2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408693	F	MP:0001926	female infertility	Syce2<em1(IMPC)Tcp>/Syce2<em1(IMPC)Tcp>	C57BL/6N-Syce2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408693	F	MP:0010024	increased total body fat amount	Syce2<em1(IMPC)Tcp>/Syce2<em1(IMPC)Tcp>	C57BL/6N-Syce2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408693	F	MP:0002989	small kidney	Syce2<em1(IMPC)Tcp>/Syce2<em1(IMPC)Tcp>	C57BL/6N-Syce2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408693	M	MP:0011874	enlarged urinary bladder	Syce2<em1(IMPC)Tcp>/Syce2<em1(IMPC)Tcp>	C57BL/6N-Syce2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408693	F	MP:0010124	decreased bone mineral content	Syce2<em1(IMPC)Tcp>/Syce2<em1(IMPC)Tcp>	C57BL/6N-Syce2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408693	M	MP:0002060	abnormal skin morphology	Syce2<em1(IMPC)Tcp>/Syce2<em1(IMPC)Tcp>	C57BL/6N-Syce2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408693	F	MP:0000063	decreased bone mineral density	Syce2<em1(IMPC)Tcp>/Syce2<em1(IMPC)Tcp>	C57BL/6N-Syce2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408693	F	MP:0010053	decreased grip strength	Syce2<em1(IMPC)Tcp>/Syce2<em1(IMPC)Tcp>	C57BL/6N-Syce2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408694	M	MP:0010088	decreased circulating fructosamine level	Syt4<em2(IMPC)H>/Syt4<em2(IMPC)H>	C57BL/6N-Syt4<em2(IMPC)H>/H	N	MGI:5576271
MGI:6408694	F	MP:0005565	increased blood urea nitrogen level	Syt4<em2(IMPC)H>/Syt4<em2(IMPC)H>	C57BL/6N-Syt4<em2(IMPC)H>/H	N	MGI:5576271
MGI:6408694	M	MP:0005419	decreased circulating serum albumin level	Syt4<em2(IMPC)H>/Syt4<em2(IMPC)H>	C57BL/6N-Syt4<em2(IMPC)H>/H	N	MGI:5576271
MGI:6408695	M	MP:0001147	small testis	Tacstd2<em1(IMPC)Mbp>/Tacstd2<em1(IMPC)Mbp>	C57BL/6N-Tacstd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408695	M	MP:0001417	decreased exploration in new environment	Tacstd2<em1(IMPC)Mbp>/Tacstd2<em1(IMPC)Mbp>	C57BL/6N-Tacstd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408695	M	MP:0001146	abnormal testis morphology	Tacstd2<em1(IMPC)Mbp>/Tacstd2<em1(IMPC)Mbp>	C57BL/6N-Tacstd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408695	F	MP:0002092	abnormal eye morphology	Tacstd2<em1(IMPC)Mbp>/Tacstd2<em1(IMPC)Mbp>	C57BL/6N-Tacstd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408695	F	MP:0001297	microphthalmia	Tacstd2<em1(IMPC)Mbp>/Tacstd2<em1(IMPC)Mbp>	C57BL/6N-Tacstd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408699	M	MP:0020421	increased freezing behavior	Tafa2<em1(IMPC)H>/Tafa2<em1(IMPC)H>	C57BL/6NTac-Tafa2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408699	F	MP:0013278	decreased fasting circulating glucose level	Tafa2<em1(IMPC)H>/Tafa2<em1(IMPC)H>	C57BL/6NTac-Tafa2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408699	M	MP:0000745	tremors	Tafa2<em1(IMPC)H>/Tafa2<em1(IMPC)H>	C57BL/6NTac-Tafa2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408700	F	MP:0000691	enlarged spleen	Tagln2<em1(IMPC)Tcp>/Tagln2<em1(IMPC)Tcp>	C57BL/6N-Tagln2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408700	M	MP:0002599	increased mean platelet volume	Tagln2<em1(IMPC)Tcp>/Tagln2<em1(IMPC)Tcp>	C57BL/6N-Tagln2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408700	M	MP:0002060	abnormal skin morphology	Tagln2<em1(IMPC)Tcp>/Tagln2<em1(IMPC)Tcp>	C57BL/6N-Tagln2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408700	M	MP:0000157	abnormal sternum morphology	Tagln2<em1(IMPC)Tcp>/Tagln2<em1(IMPC)Tcp>	C57BL/6N-Tagln2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408700	F	MP:0002574	increased vertical activity	Tagln2<em1(IMPC)Tcp>/Tagln2<em1(IMPC)Tcp>	C57BL/6N-Tagln2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408700	M	MP:0010067	increased red blood cell distribution width	Tagln2<em1(IMPC)Tcp>/Tagln2<em1(IMPC)Tcp>	C57BL/6N-Tagln2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408700	M	MP:0000219	increased neutrophil cell number	Tagln2<em1(IMPC)Tcp>/Tagln2<em1(IMPC)Tcp>	C57BL/6N-Tagln2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408700	M	MP:0005016	decreased lymphocyte cell number	Tagln2<em1(IMPC)Tcp>/Tagln2<em1(IMPC)Tcp>	C57BL/6N-Tagln2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408701	M	MP:0009455	enhanced cued conditioning behavior	Tasor<em1(IMPC)Ccpcz>/Tasor<+>	C57BL/6N-Tasor<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408703	M	MP:0002833	increased heart weight	Tbc1d20<em1(IMPC)Mbp>/Tbc1d20<+>	C57BL/6N-Tbc1d20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408703	M	MP:0010067	increased red blood cell distribution width	Tbc1d20<em1(IMPC)Mbp>/Tbc1d20<+>	C57BL/6N-Tbc1d20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408703	M	MP:0002060	abnormal skin morphology	Tbc1d20<em1(IMPC)Mbp>/Tbc1d20<+>	C57BL/6N-Tbc1d20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408704	M	MP:0001925	male infertility	Tbc1d20<em1(IMPC)Mbp>/Tbc1d20<em1(IMPC)Mbp>	C57BL/6N-Tbc1d20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408705	F	MP:0003232	abnormal forebrain development	Tbx20<em1(IMPC)Mbp>/Tbx20<em1(IMPC)Mbp>	C57BL/6N-Tbx20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408705	F	MP:0003720	abnormal neural tube closure	Tbx20<em1(IMPC)Mbp>/Tbx20<em1(IMPC)Mbp>	C57BL/6N-Tbx20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408706	F	MP:0000288	abnormal pericardium morphology	Tek<tm1b(EUCOMM)Hmgu>/Tek<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tek<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6408707	F	MP:0005084	abnormal gallbladder morphology	Tent4a<tm1b(EUCOMM)Hmgu>/Tent4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tent4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408707	F	MP:0001364	decreased anxiety-related response	Tent4a<tm1b(EUCOMM)Hmgu>/Tent4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tent4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408707	F	MP:0004599	abnormal vertebral arch morphology	Tent4a<tm1b(EUCOMM)Hmgu>/Tent4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tent4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408707	M	MP:0001146	abnormal testis morphology	Tent4a<tm1b(EUCOMM)Hmgu>/Tent4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tent4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408707	F	MP:0009342	enlarged gallbladder	Tent4a<tm1b(EUCOMM)Hmgu>/Tent4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tent4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408707	M	MP:0001147	small testis	Tent4a<tm1b(EUCOMM)Hmgu>/Tent4a<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tent4a<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408708	M	MP:0000458	abnormal mandible morphology	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	M	MP:0005627	increased circulating potassium level	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	F	MP:0000161	scoliosis	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	F	MP:0001303	abnormal lens morphology	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	M	MP:0001523	impaired righting response	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	F	MP:0020421	increased freezing behavior	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	F	MP:0000219	increased neutrophil cell number	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	F	MP:0000322	increased granulocyte number	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	F	MP:0005016	decreased lymphocyte cell number	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	F	MP:0005419	decreased circulating serum albumin level	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	M	MP:0001406	abnormal gait	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	F	MP:0000220	increased monocyte cell number	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	M	MP:0000558	abnormal tibia morphology	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	F	MP:0002764	short tibia	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	M	MP:0010379	decreased respiratory quotient	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	M	MP:0002187	abnormal fibula morphology	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	M	MP:0000559	abnormal femur morphology	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	M	MP:0009455	enhanced cued conditioning behavior	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408708	F	MP:0000218	increased leukocyte cell number	Tent5a<em1(IMPC)Ccpcz>/Tent5a<em1(IMPC)Ccpcz>	C57BL/6N-Tent5a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408709	M	MP:0001192	scaly skin	Terf2ip<em1(IMPC)Mbp>/Terf2ip<em1(IMPC)Mbp>	C57BL/6N-Terf2ip<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408710	F	MP:0000218	increased leukocyte cell number	Tex261<tm1b(EUCOMM)Wtsi>/Tex261<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tex261<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408710	F	MP:0002968	increased circulating alkaline phosphatase level	Tex261<tm1b(EUCOMM)Wtsi>/Tex261<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tex261<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408710	F	MP:0005343	increased circulating aspartate transaminase level	Tex261<tm1b(EUCOMM)Wtsi>/Tex261<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tex261<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408710	M	MP:0010025	decreased total body fat amount	Tex261<tm1b(EUCOMM)Wtsi>/Tex261<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tex261<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408710	F	MP:0010088	decreased circulating fructosamine level	Tex261<tm1b(EUCOMM)Wtsi>/Tex261<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tex261<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408710	M	MP:0005419	decreased circulating serum albumin level	Tex261<tm1b(EUCOMM)Wtsi>/Tex261<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tex261<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408710	M	MP:0003960	increased lean body mass	Tex261<tm1b(EUCOMM)Wtsi>/Tex261<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tex261<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408710	M	MP:0005567	decreased circulating total protein level	Tex261<tm1b(EUCOMM)Wtsi>/Tex261<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tex261<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408710	F	MP:0000183	decreased circulating LDL cholesterol level	Tex261<tm1b(EUCOMM)Wtsi>/Tex261<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tex261<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408710	M	MP:0000195	decreased circulating calcium level	Tex261<tm1b(EUCOMM)Wtsi>/Tex261<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tex261<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408710	M	MP:0000062	increased bone mineral density	Tex261<tm1b(EUCOMM)Wtsi>/Tex261<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tex261<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408710	M	MP:0010123	increased bone mineral content	Tex261<tm1b(EUCOMM)Wtsi>/Tex261<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tex261<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408710	F	MP:0002941	increased circulating alanine transaminase level	Tex261<tm1b(EUCOMM)Wtsi>/Tex261<tm1b(EUCOMM)Wtsi>	C57BL/6N-Tex261<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408711	M	MP:0001258	decreased body length	Tex2<tm1.1(KOMP)Vlcg>/Tex2<tm1.1(KOMP)Vlcg>	C57BL/6N-Tex2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6408711	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Tex2<tm1.1(KOMP)Vlcg>/Tex2<tm1.1(KOMP)Vlcg>	C57BL/6N-Tex2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6408711	M	MP:0001303	abnormal lens morphology	Tex2<tm1.1(KOMP)Vlcg>/Tex2<tm1.1(KOMP)Vlcg>	C57BL/6N-Tex2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6408711	M	MP:0002941	increased circulating alanine transaminase level	Tex2<tm1.1(KOMP)Vlcg>/Tex2<tm1.1(KOMP)Vlcg>	C57BL/6N-Tex2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6408711	F	MP:0002591	decreased mean corpuscular volume	Tex2<tm1.1(KOMP)Vlcg>/Tex2<tm1.1(KOMP)Vlcg>	C57BL/6N-Tex2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6408711	F	MP:0005344	increased circulating bilirubin level	Tex2<tm1.1(KOMP)Vlcg>/Tex2<tm1.1(KOMP)Vlcg>	C57BL/6N-Tex2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6408712	F	MP:0002874	decreased hemoglobin content	Tfrc<em1(IMPC)H>/Tfrc<+>	C57BL/6N-Tfrc<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408712	F	MP:0001529	abnormal vocalization	Tfrc<em1(IMPC)H>/Tfrc<+>	C57BL/6N-Tfrc<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408712	M	MP:0001406	abnormal gait	Tfrc<em1(IMPC)H>/Tfrc<+>	C57BL/6N-Tfrc<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408714	M	MP:0002135	abnormal kidney morphology	Tgfbr3<em1(IMPC)Mbp>/Tgfbr3<+>	C57BL/6N-Tgfbr3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408714	M	MP:0003068	enlarged kidney	Tgfbr3<em1(IMPC)Mbp>/Tgfbr3<+>	C57BL/6N-Tgfbr3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408715	M	MP:0003984	embryonic growth retardation	Tgfbr3<em1(IMPC)Mbp>/Tgfbr3<em1(IMPC)Mbp>	C57BL/6N-Tgfbr3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408716	M	MP:0000266	abnormal heart morphology	Timp4<em1(IMPC)Mbp>/Timp4<em1(IMPC)Mbp>	C57BL/6N-Timp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408716	F	MP:0000692	small spleen	Timp4<em1(IMPC)Mbp>/Timp4<em1(IMPC)Mbp>	C57BL/6N-Timp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408716	F	MP:0002060	abnormal skin morphology	Timp4<em1(IMPC)Mbp>/Timp4<em1(IMPC)Mbp>	C57BL/6N-Timp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408716	F	MP:0001333	absent optic nerve	Timp4<em1(IMPC)Mbp>/Timp4<em1(IMPC)Mbp>	C57BL/6N-Timp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408716	M	MP:0020421	increased freezing behavior	Timp4<em1(IMPC)Mbp>/Timp4<em1(IMPC)Mbp>	C57BL/6N-Timp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408716	M	MP:0002188	small heart	Timp4<em1(IMPC)Mbp>/Timp4<em1(IMPC)Mbp>	C57BL/6N-Timp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408717	M	MP:0005419	decreased circulating serum albumin level	Tm7sf2<tm1b(KOMP)Wtsi>/Tm7sf2<tm1b(KOMP)Wtsi>	C57BL/6N-Tm7sf2<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408717	M	MP:0002574	increased vertical activity	Tm7sf2<tm1b(KOMP)Wtsi>/Tm7sf2<tm1b(KOMP)Wtsi>	C57BL/6N-Tm7sf2<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408717	F	MP:0005016	decreased lymphocyte cell number	Tm7sf2<tm1b(KOMP)Wtsi>/Tm7sf2<tm1b(KOMP)Wtsi>	C57BL/6N-Tm7sf2<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408717	F	MP:0005011	increased eosinophil cell number	Tm7sf2<tm1b(KOMP)Wtsi>/Tm7sf2<tm1b(KOMP)Wtsi>	C57BL/6N-Tm7sf2<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6408719	F	MP:0005344	increased circulating bilirubin level	Tmem115<tm1(KOMP)Vlcg>/Tmem115<+>	C57BL/6N-Tmem115<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408719	M	MP:0003917	increased kidney weight	Tmem115<tm1(KOMP)Vlcg>/Tmem115<+>	C57BL/6N-Tmem115<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408719	M	MP:0003960	increased lean body mass	Tmem115<tm1(KOMP)Vlcg>/Tmem115<+>	C57BL/6N-Tmem115<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6408721	M	MP:0005343	increased circulating aspartate transaminase level	Tmem11<em1(IMPC)Tcp>/Tmem11<em1(IMPC)Tcp>	C57BL/6N-Tmem11<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408721	M	MP:0002060	abnormal skin morphology	Tmem11<em1(IMPC)Tcp>/Tmem11<em1(IMPC)Tcp>	C57BL/6N-Tmem11<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408722	F	MP:0005278	abnormal cholesterol homeostasis	Tmem132b<em1(IMPC)Ccpcz>/Tmem132b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem132b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408722	M	MP:0001417	decreased exploration in new environment	Tmem132b<em1(IMPC)Ccpcz>/Tmem132b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem132b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408722	F	MP:0010896	decreased lung compliance	Tmem132b<em1(IMPC)Ccpcz>/Tmem132b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem132b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408722	F	MP:0001399	hyperactivity	Tmem132b<em1(IMPC)Ccpcz>/Tmem132b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem132b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408722	F	MP:0001260	increased body weight	Tmem132b<em1(IMPC)Ccpcz>/Tmem132b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem132b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408722	F	MP:0000598	abnormal liver morphology	Tmem132b<em1(IMPC)Ccpcz>/Tmem132b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem132b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408723	F	MP:0000598	abnormal liver morphology	Tmem150b<em1(IMPC)Ccpcz>/Tmem150b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem150b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408723	M	MP:0001284	absent vibrissae	Tmem150b<em1(IMPC)Ccpcz>/Tmem150b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem150b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408723	M	MP:0003068	enlarged kidney	Tmem150b<em1(IMPC)Ccpcz>/Tmem150b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem150b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408723	F	MP:0001325	abnormal retina morphology	Tmem150b<em1(IMPC)Ccpcz>/Tmem150b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem150b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408723	F	MP:0013522	decreased memory-marker CD4-positive NK T cell number	Tmem150b<em1(IMPC)Ccpcz>/Tmem150b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem150b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408723	F	MP:0020421	increased freezing behavior	Tmem150b<em1(IMPC)Ccpcz>/Tmem150b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem150b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408723	F	MP:0001303	abnormal lens morphology	Tmem150b<em1(IMPC)Ccpcz>/Tmem150b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem150b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408723	M	MP:0002135	abnormal kidney morphology	Tmem150b<em1(IMPC)Ccpcz>/Tmem150b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem150b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408723	F	MP:0002098	abnormal vibrissa morphology	Tmem150b<em1(IMPC)Ccpcz>/Tmem150b<em1(IMPC)Ccpcz>	C57BL/6N-Tmem150b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408724	F	MP:0001258	decreased body length	Tmem178b<tm1a(KOMP)Wtsi>/Tmem178b<tm1a(KOMP)Wtsi>	C57BL/6N-Tmem178b<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408725	M	MP:0001147	small testis	Tmem237<tm1b(EUCOMM)Hmgu>/Tmem237<+>	C57BL/6N-Tmem237<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408725	F	MP:0000194	increased circulating calcium level	Tmem237<tm1b(EUCOMM)Hmgu>/Tmem237<+>	C57BL/6N-Tmem237<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408725	M	MP:0000639	abnormal adrenal gland morphology	Tmem237<tm1b(EUCOMM)Hmgu>/Tmem237<+>	C57BL/6N-Tmem237<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408725	F	MP:0005238	increased brain size	Tmem237<tm1b(EUCOMM)Hmgu>/Tmem237<+>	C57BL/6N-Tmem237<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408725	M	MP:0000627	abnormal mammary gland morphology	Tmem237<tm1b(EUCOMM)Hmgu>/Tmem237<+>	C57BL/6N-Tmem237<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408725	F	MP:0002968	increased circulating alkaline phosphatase level	Tmem237<tm1b(EUCOMM)Hmgu>/Tmem237<+>	C57BL/6N-Tmem237<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408725	F	MP:0000702	enlarged lymph nodes	Tmem237<tm1b(EUCOMM)Hmgu>/Tmem237<+>	C57BL/6N-Tmem237<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408725	M	MP:0020421	increased freezing behavior	Tmem237<tm1b(EUCOMM)Hmgu>/Tmem237<+>	C57BL/6N-Tmem237<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408725	M	MP:0004357	long tibia	Tmem237<tm1b(EUCOMM)Hmgu>/Tmem237<+>	C57BL/6N-Tmem237<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408725	M	MP:0002768	small adrenal glands	Tmem237<tm1b(EUCOMM)Hmgu>/Tmem237<+>	C57BL/6N-Tmem237<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408725	M	MP:0001146	abnormal testis morphology	Tmem237<tm1b(EUCOMM)Hmgu>/Tmem237<+>	C57BL/6N-Tmem237<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408725	F	MP:0002339	abnormal lymph node morphology	Tmem237<tm1b(EUCOMM)Hmgu>/Tmem237<+>	C57BL/6N-Tmem237<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408727	M	MP:0013279	increased fasting circulating glucose level	Tmem240<em1(IMPC)Ccpcz>/Tmem240<em1(IMPC)Ccpcz>	C57BL/6N-Tmem240<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408727	M	MP:0000598	abnormal liver morphology	Tmem240<em1(IMPC)Ccpcz>/Tmem240<em1(IMPC)Ccpcz>	C57BL/6N-Tmem240<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408727	F	MP:0001392	abnormal locomotor behavior	Tmem240<em1(IMPC)Ccpcz>/Tmem240<em1(IMPC)Ccpcz>	C57BL/6N-Tmem240<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408727	M	MP:0001146	abnormal testis morphology	Tmem240<em1(IMPC)Ccpcz>/Tmem240<em1(IMPC)Ccpcz>	C57BL/6N-Tmem240<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408727	F	MP:0002968	increased circulating alkaline phosphatase level	Tmem240<em1(IMPC)Ccpcz>/Tmem240<em1(IMPC)Ccpcz>	C57BL/6N-Tmem240<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408727	M	MP:0000745	tremors	Tmem240<em1(IMPC)Ccpcz>/Tmem240<em1(IMPC)Ccpcz>	C57BL/6N-Tmem240<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408727	M	MP:0001147	small testis	Tmem240<em1(IMPC)Ccpcz>/Tmem240<em1(IMPC)Ccpcz>	C57BL/6N-Tmem240<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408728	M	MP:0002100	abnormal tooth morphology	Tmem273<em1(IMPC)Ccpcz>/Tmem273<em1(IMPC)Ccpcz>	C57BL/6N-Tmem273<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408728	M	MP:0003036	vertebral transformation	Tmem273<em1(IMPC)Ccpcz>/Tmem273<em1(IMPC)Ccpcz>	C57BL/6N-Tmem273<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408728	M	MP:0003795	abnormal bone structure	Tmem273<em1(IMPC)Ccpcz>/Tmem273<em1(IMPC)Ccpcz>	C57BL/6N-Tmem273<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408728	M	MP:0000137	abnormal vertebrae morphology	Tmem273<em1(IMPC)Ccpcz>/Tmem273<em1(IMPC)Ccpcz>	C57BL/6N-Tmem273<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408728	M	MP:0002135	abnormal kidney morphology	Tmem273<em1(IMPC)Ccpcz>/Tmem273<em1(IMPC)Ccpcz>	C57BL/6N-Tmem273<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408732	M	MP:0002135	abnormal kidney morphology	Tmem60<em1(IMPC)Ccpcz>/Tmem60<em1(IMPC)Ccpcz>	C57BL/6N-Tmem60<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408732	F	MP:0013771	decreased effector memory T-helper cell number	Tmem60<em1(IMPC)Ccpcz>/Tmem60<em1(IMPC)Ccpcz>	C57BL/6N-Tmem60<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408732	M	MP:0003233	prolonged QT interval	Tmem60<em1(IMPC)Ccpcz>/Tmem60<em1(IMPC)Ccpcz>	C57BL/6N-Tmem60<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408732	M	MP:0010506	prolonged RR interval	Tmem60<em1(IMPC)Ccpcz>/Tmem60<em1(IMPC)Ccpcz>	C57BL/6N-Tmem60<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408732	M	MP:0005333	decreased heart rate	Tmem60<em1(IMPC)Ccpcz>/Tmem60<em1(IMPC)Ccpcz>	C57BL/6N-Tmem60<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408732	M	MP:0001364	decreased anxiety-related response	Tmem60<em1(IMPC)Ccpcz>/Tmem60<em1(IMPC)Ccpcz>	C57BL/6N-Tmem60<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408732	M	MP:0001925	male infertility	Tmem60<em1(IMPC)Ccpcz>/Tmem60<em1(IMPC)Ccpcz>	C57BL/6N-Tmem60<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408736	F	MP:0005292	improved glucose tolerance	Tpo<em1(IMPC)H>/Tpo<+>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0000550	abnormal forelimb morphology	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0005343	increased circulating aspartate transaminase level	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0000745	tremors	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0001417	decreased exploration in new environment	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0001523	impaired righting response	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0002968	increased circulating alkaline phosphatase level	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0000556	abnormal hindlimb morphology	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0001406	abnormal gait	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0005553	increased circulating creatinine level	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0001513	limb grasping	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0000367	abnormal coat/ hair morphology	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0005178	increased circulating cholesterol level	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0001486	abnormal startle reflex	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408737	M	MP:0008810	increased circulating iron level	Tpo<em1(IMPC)H>/Tpo<em1(IMPC)H>	C57BL/6NTac-Tpo<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408738	M	MP:0001891	hydrocephaly	Trabd2b<em2(IMPC)Ccpcz>/Trabd2b<em2(IMPC)Ccpcz>	C57BL/6N-Trabd2b<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408738	F	MP:0000639	abnormal adrenal gland morphology	Trabd2b<em2(IMPC)Ccpcz>/Trabd2b<em2(IMPC)Ccpcz>	C57BL/6N-Trabd2b<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408738	M	MP:0002953	thick ventricular wall	Trabd2b<em2(IMPC)Ccpcz>/Trabd2b<em2(IMPC)Ccpcz>	C57BL/6N-Trabd2b<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408738	F	MP:0000642	enlarged adrenal glands	Trabd2b<em2(IMPC)Ccpcz>/Trabd2b<em2(IMPC)Ccpcz>	C57BL/6N-Trabd2b<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408738	M	MP:0002152	abnormal brain morphology	Trabd2b<em2(IMPC)Ccpcz>/Trabd2b<em2(IMPC)Ccpcz>	C57BL/6N-Trabd2b<em2(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408739	F	MP:0002092	abnormal eye morphology	Trap1<em1(IMPC)Mbp>/Trap1<em1(IMPC)Mbp>	C57BL/6N-Trap1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408739	F	MP:0005554	decreased circulating creatinine level	Trap1<em1(IMPC)Mbp>/Trap1<em1(IMPC)Mbp>	C57BL/6N-Trap1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408739	F	MP:0000198	decreased circulating phosphate level	Trap1<em1(IMPC)Mbp>/Trap1<em1(IMPC)Mbp>	C57BL/6N-Trap1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408740	F	MP:0008935	decreased mean platelet volume	Trdmt1<tm1b(EUCOMM)Hmgu>/Trdmt1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trdmt1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408740	M	MP:0001399	hyperactivity	Trdmt1<tm1b(EUCOMM)Hmgu>/Trdmt1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trdmt1<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6408741	M	MP:0002768	small adrenal glands	Trim13<em1(IMPC)Tcp>/Trim13<em1(IMPC)Tcp>	C57BL/6N-Trim13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408741	F	MP:0000627	abnormal mammary gland morphology	Trim13<em1(IMPC)Tcp>/Trim13<em1(IMPC)Tcp>	C57BL/6N-Trim13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408741	M	MP:0011874	enlarged urinary bladder	Trim13<em1(IMPC)Tcp>/Trim13<em1(IMPC)Tcp>	C57BL/6N-Trim13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408741	M	MP:0001552	increased circulating triglyceride level	Trim13<em1(IMPC)Tcp>/Trim13<em1(IMPC)Tcp>	C57BL/6N-Trim13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408741	F	MP:0002637	small uterus	Trim13<em1(IMPC)Tcp>/Trim13<em1(IMPC)Tcp>	C57BL/6N-Trim13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408741	F	MP:0000709	enlarged thymus	Trim13<em1(IMPC)Tcp>/Trim13<em1(IMPC)Tcp>	C57BL/6N-Trim13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408741	M	MP:0002059	abnormal seminal vesicle morphology	Trim13<em1(IMPC)Tcp>/Trim13<em1(IMPC)Tcp>	C57BL/6N-Trim13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408742	M	MP:0001529	abnormal vocalization	Trim15<tm1b(EUCOMM)Hmgu>/Trim15<tm1b(EUCOMM)Hmgu>	C57BL/6N-Trim15<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6408743	M	MP:0005634	decreased circulating sodium level	Trim9<em1(IMPC)Ccpcz>/Trim9<em1(IMPC)Ccpcz>	C57BL/6N-Trim9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408743	M	MP:0013771	decreased effector memory T-helper cell number	Trim9<em1(IMPC)Ccpcz>/Trim9<em1(IMPC)Ccpcz>	C57BL/6N-Trim9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408743	M	MP:0001158	abnormal prostate gland morphology	Trim9<em1(IMPC)Ccpcz>/Trim9<em1(IMPC)Ccpcz>	C57BL/6N-Trim9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408743	M	MP:0002774	small prostate gland	Trim9<em1(IMPC)Ccpcz>/Trim9<em1(IMPC)Ccpcz>	C57BL/6N-Trim9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408743	M	MP:0002135	abnormal kidney morphology	Trim9<em1(IMPC)Ccpcz>/Trim9<em1(IMPC)Ccpcz>	C57BL/6N-Trim9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408743	M	MP:0004953	decreased spleen weight	Trim9<em1(IMPC)Ccpcz>/Trim9<em1(IMPC)Ccpcz>	C57BL/6N-Trim9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408743	M	MP:0003068	enlarged kidney	Trim9<em1(IMPC)Ccpcz>/Trim9<em1(IMPC)Ccpcz>	C57BL/6N-Trim9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408743	M	MP:0001175	abnormal lung morphology	Trim9<em1(IMPC)Ccpcz>/Trim9<em1(IMPC)Ccpcz>	C57BL/6N-Trim9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408743	M	MP:0004599	abnormal vertebral arch morphology	Trim9<em1(IMPC)Ccpcz>/Trim9<em1(IMPC)Ccpcz>	C57BL/6N-Trim9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6408744	M	MP:0001304	cataract	Trmt9b<em1(IMPC)H>/Trmt9b<em1(IMPC)H>	C57BL/6NTac-Trmt9b<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408745	F	MP:0001529	abnormal vocalization	Tspan11<tm2b(EUCOMM)Wtsi>/Tspan11<tm2b(EUCOMM)Wtsi>	C57BL/6N-Tspan11<tm2b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408745	M	MP:0000367	abnormal coat/ hair morphology	Tspan11<tm2b(EUCOMM)Wtsi>/Tspan11<tm2b(EUCOMM)Wtsi>	C57BL/6N-Tspan11<tm2b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408746	M	MP:0005565	increased blood urea nitrogen level	Tspoap1<em1(IMPC)H>/Tspoap1<em1(IMPC)H>	C57BL/6N-Tspoap1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408746	M	MP:0009142	decreased prepulse inhibition	Tspoap1<em1(IMPC)H>/Tspoap1<em1(IMPC)H>	C57BL/6N-Tspoap1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408746	F	MP:0005567	decreased circulating total protein level	Tspoap1<em1(IMPC)H>/Tspoap1<em1(IMPC)H>	C57BL/6N-Tspoap1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408746	F	MP:0010052	increased grip strength	Tspoap1<em1(IMPC)H>/Tspoap1<em1(IMPC)H>	C57BL/6N-Tspoap1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408746	F	MP:0002968	increased circulating alkaline phosphatase level	Tspoap1<em1(IMPC)H>/Tspoap1<em1(IMPC)H>	C57BL/6N-Tspoap1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408748	M	MP:0000706	small thymus	Ubd<tm1b(EUCOMM)Wtsi>/Ubd<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ubd<tm1b(EUCOMM)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408748	F	MP:0013883	increased CD4-positive, CD25-positive NK T cell number	Ubd<tm1b(EUCOMM)Wtsi>/Ubd<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ubd<tm1b(EUCOMM)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408748	F	MP:0013522	decreased memory-marker CD4-positive NK T cell number	Ubd<tm1b(EUCOMM)Wtsi>/Ubd<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ubd<tm1b(EUCOMM)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408748	M	MP:0000703	abnormal thymus morphology	Ubd<tm1b(EUCOMM)Wtsi>/Ubd<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ubd<tm1b(EUCOMM)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408748	M	MP:0002059	abnormal seminal vesicle morphology	Ubd<tm1b(EUCOMM)Wtsi>/Ubd<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ubd<tm1b(EUCOMM)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6408749	M	MP:0005561	increased mean corpuscular hemoglobin	Ube2d1<tm3e(EUCOMM)Wtsi>/Ube2d1<tm3e(EUCOMM)Wtsi>	C57BL/6N-Ube2d1<tm3e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408749	M	MP:0002599	increased mean platelet volume	Ube2d1<tm3e(EUCOMM)Wtsi>/Ube2d1<tm3e(EUCOMM)Wtsi>	C57BL/6N-Ube2d1<tm3e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408749	M	MP:0005179	decreased circulating cholesterol level	Ube2d1<tm3e(EUCOMM)Wtsi>/Ube2d1<tm3e(EUCOMM)Wtsi>	C57BL/6N-Ube2d1<tm3e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408749	M	MP:0005344	increased circulating bilirubin level	Ube2d1<tm3e(EUCOMM)Wtsi>/Ube2d1<tm3e(EUCOMM)Wtsi>	C57BL/6N-Ube2d1<tm3e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408750	M	MP:0011940	decreased food intake	Ube3a<em1(IMPC)Hmgu>/Ube3a<+>	C57BL/6N-Ube3a<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408750	M	MP:0010379	decreased respiratory quotient	Ube3a<em1(IMPC)Hmgu>/Ube3a<+>	C57BL/6N-Ube3a<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408751	F	MP:0010024	increased total body fat amount	Ube3a<em1(IMPC)Hmgu>/Ube3a<em1(IMPC)Hmgu>	C57BL/6N-Ube3a<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408751	F	MP:0010124	decreased bone mineral content	Ube3a<em1(IMPC)Hmgu>/Ube3a<em1(IMPC)Hmgu>	C57BL/6N-Ube3a<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408751	M	MP:0002059	abnormal seminal vesicle morphology	Ube3a<em1(IMPC)Hmgu>/Ube3a<em1(IMPC)Hmgu>	C57BL/6N-Ube3a<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408752	F	MP:0002884	abnormal pharyngeal arch morphology	Uggt1<em1(IMPC)Mbp>/Uggt1<em1(IMPC)Mbp>	C57BL/6N-Uggt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408752	M	MP:0001711	abnormal placenta morphology	Uggt1<em1(IMPC)Mbp>/Uggt1<em1(IMPC)Mbp>	C57BL/6N-Uggt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408752	F	MP:0003720	abnormal neural tube closure	Uggt1<em1(IMPC)Mbp>/Uggt1<em1(IMPC)Mbp>	C57BL/6N-Uggt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408756	M	MP:0001489	decreased startle reflex	Usp31<em1(IMPC)H>/Usp31<em1(IMPC)H>	C57BL/6NTac-Usp31<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408756	F	MP:0000745	tremors	Usp31<em1(IMPC)H>/Usp31<em1(IMPC)H>	C57BL/6NTac-Usp31<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408756	F	MP:0006243	impaired pupillary reflex	Usp31<em1(IMPC)H>/Usp31<em1(IMPC)H>	C57BL/6NTac-Usp31<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408757	F	MP:0005344	increased circulating bilirubin level	Usp53<em1(IMPC)Tcp>/Usp53<em1(IMPC)Tcp>	C57BL/6N-Usp53<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408757	M	MP:0001489	decreased startle reflex	Usp53<em1(IMPC)Tcp>/Usp53<em1(IMPC)Tcp>	C57BL/6N-Usp53<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408757	M	MP:0005178	increased circulating cholesterol level	Usp53<em1(IMPC)Tcp>/Usp53<em1(IMPC)Tcp>	C57BL/6N-Usp53<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408757	F	MP:0000367	abnormal coat/ hair morphology	Usp53<em1(IMPC)Tcp>/Usp53<em1(IMPC)Tcp>	C57BL/6N-Usp53<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408757	M	MP:0005568	increased circulating total protein level	Usp53<em1(IMPC)Tcp>/Usp53<em1(IMPC)Tcp>	C57BL/6N-Usp53<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408758	M	MP:0000598	abnormal liver morphology	Vdac3<em1(IMPC)Hmgu>/Vdac3<em1(IMPC)Hmgu>	C57BL/6N-Vdac3<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408758	M	MP:0003233	prolonged QT interval	Vdac3<em1(IMPC)Hmgu>/Vdac3<em1(IMPC)Hmgu>	C57BL/6N-Vdac3<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408758	M	MP:0001510	abnormal coat appearance	Vdac3<em1(IMPC)Hmgu>/Vdac3<em1(IMPC)Hmgu>	C57BL/6N-Vdac3<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6408759	F	MP:0002966	decreased circulating alkaline phosphatase level	Vps13b<em1(IMPC)Tcp>/Vps13b<em1(IMPC)Tcp>	C57BL/6N-Vps13b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408759	M	MP:0001925	male infertility	Vps13b<em1(IMPC)Tcp>/Vps13b<em1(IMPC)Tcp>	C57BL/6N-Vps13b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408759	M	MP:0001488	increased startle reflex	Vps13b<em1(IMPC)Tcp>/Vps13b<em1(IMPC)Tcp>	C57BL/6N-Vps13b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408759	M	MP:0003961	decreased lean body mass	Vps13b<em1(IMPC)Tcp>/Vps13b<em1(IMPC)Tcp>	C57BL/6N-Vps13b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408759	F	MP:0005293	impaired glucose tolerance	Vps13b<em1(IMPC)Tcp>/Vps13b<em1(IMPC)Tcp>	C57BL/6N-Vps13b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408759	F	MP:0002590	increased mean corpuscular volume	Vps13b<em1(IMPC)Tcp>/Vps13b<em1(IMPC)Tcp>	C57BL/6N-Vps13b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408759	M	MP:0010052	increased grip strength	Vps13b<em1(IMPC)Tcp>/Vps13b<em1(IMPC)Tcp>	C57BL/6N-Vps13b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408759	F	MP:0001258	decreased body length	Vps13b<em1(IMPC)Tcp>/Vps13b<em1(IMPC)Tcp>	C57BL/6N-Vps13b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408759	M	MP:0000692	small spleen	Vps13b<em1(IMPC)Tcp>/Vps13b<em1(IMPC)Tcp>	C57BL/6N-Vps13b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408759	F	MP:0000702	enlarged lymph nodes	Vps13b<em1(IMPC)Tcp>/Vps13b<em1(IMPC)Tcp>	C57BL/6N-Vps13b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408759	M	MP:0002188	small heart	Vps13b<em1(IMPC)Tcp>/Vps13b<em1(IMPC)Tcp>	C57BL/6N-Vps13b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408759	M	MP:0000598	abnormal liver morphology	Vps13b<em1(IMPC)Tcp>/Vps13b<em1(IMPC)Tcp>	C57BL/6N-Vps13b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408759	M	MP:0010024	increased total body fat amount	Vps13b<em1(IMPC)Tcp>/Vps13b<em1(IMPC)Tcp>	C57BL/6N-Vps13b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408760	M	MP:0001406	abnormal gait	Vps35<em1(IMPC)H>/Vps35<+>	C57BL/6N-Vps35<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408760	M	MP:0001325	abnormal retina morphology	Vps35<em1(IMPC)H>/Vps35<+>	C57BL/6N-Vps35<em1(IMPC)H>/H	N	MGI:5576271
MGI:6408763	F	MP:0003743	abnormal facial morphology	Wdfy3<em1(IMPC)Mbp>/Wdfy3<em1(IMPC)Mbp>	C57BL/6N-Wdfy3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408763	F	MP:0003984	embryonic growth retardation	Wdfy3<em1(IMPC)Mbp>/Wdfy3<em1(IMPC)Mbp>	C57BL/6N-Wdfy3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408763	F	MP:0000111	cleft palate	Wdfy3<em1(IMPC)Mbp>/Wdfy3<em1(IMPC)Mbp>	C57BL/6N-Wdfy3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408763	F	MP:0000428	abnormal craniofacial morphology	Wdfy3<em1(IMPC)Mbp>/Wdfy3<em1(IMPC)Mbp>	C57BL/6N-Wdfy3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408763	M	MP:0001711	abnormal placenta morphology	Wdfy3<em1(IMPC)Mbp>/Wdfy3<em1(IMPC)Mbp>	C57BL/6N-Wdfy3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408765	F	MP:0002092	abnormal eye morphology	Yipf6<em1(IMPC)Mbp>/Yipf6<em1(IMPC)Mbp>	C57BL/6N-Yipf6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408765	F	MP:0001293	anophthalmia	Yipf6<em1(IMPC)Mbp>/Yipf6<em1(IMPC)Mbp>	C57BL/6N-Yipf6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408765	F	MP:0001297	microphthalmia	Yipf6<em1(IMPC)Mbp>/Yipf6<em1(IMPC)Mbp>	C57BL/6N-Yipf6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408765	F	MP:0000220	increased monocyte cell number	Yipf6<em1(IMPC)Mbp>/Yipf6<em1(IMPC)Mbp>	C57BL/6N-Yipf6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408766	F	MP:0002100	abnormal tooth morphology	Ypel2<em1(IMPC)Tcp>/Ypel2<em1(IMPC)Tcp>	C57BL/6N-Ypel2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408766	F	MP:0001258	decreased body length	Ypel2<em1(IMPC)Tcp>/Ypel2<em1(IMPC)Tcp>	C57BL/6N-Ypel2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408766	M	MP:0003233	prolonged QT interval	Ypel2<em1(IMPC)Tcp>/Ypel2<em1(IMPC)Tcp>	C57BL/6N-Ypel2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408766	M	MP:0000157	abnormal sternum morphology	Ypel2<em1(IMPC)Tcp>/Ypel2<em1(IMPC)Tcp>	C57BL/6N-Ypel2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408766	M	MP:0011874	enlarged urinary bladder	Ypel2<em1(IMPC)Tcp>/Ypel2<em1(IMPC)Tcp>	C57BL/6N-Ypel2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408766	M	MP:0002092	abnormal eye morphology	Ypel2<em1(IMPC)Tcp>/Ypel2<em1(IMPC)Tcp>	C57BL/6N-Ypel2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408767	M	MP:0004924	abnormal behavior	Ywhab<tm1b(EUCOMM)Hmgu>/Ywhab<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ywhab<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408767	M	MP:0003179	thrombocytopenia	Ywhab<tm1b(EUCOMM)Hmgu>/Ywhab<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ywhab<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408767	M	MP:0005344	increased circulating bilirubin level	Ywhab<tm1b(EUCOMM)Hmgu>/Ywhab<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ywhab<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408767	M	MP:0004151	decreased circulating iron level	Ywhab<tm1b(EUCOMM)Hmgu>/Ywhab<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ywhab<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408767	M	MP:0005179	decreased circulating cholesterol level	Ywhab<tm1b(EUCOMM)Hmgu>/Ywhab<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ywhab<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408767	M	MP:0000186	decreased circulating HDL cholesterol level	Ywhab<tm1b(EUCOMM)Hmgu>/Ywhab<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ywhab<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408767	M	MP:0005560	decreased circulating glucose level	Ywhab<tm1b(EUCOMM)Hmgu>/Ywhab<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ywhab<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408767	M	MP:0005567	decreased circulating total protein level	Ywhab<tm1b(EUCOMM)Hmgu>/Ywhab<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ywhab<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408767	M	MP:0005566	decreased blood urea nitrogen level	Ywhab<tm1b(EUCOMM)Hmgu>/Ywhab<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ywhab<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408768	M	MP:0002098	abnormal vibrissa morphology	Zbed5<tm1b(EUCOMM)Wtsi>/Zbed5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zbed5<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408769	M	MP:0001925	male infertility	Zcwpw1<em1(IMPC)Tcp>/Zcwpw1<em1(IMPC)Tcp>	C57BL/6N-Zcwpw1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408769	M	MP:0001147	small testis	Zcwpw1<em1(IMPC)Tcp>/Zcwpw1<em1(IMPC)Tcp>	C57BL/6N-Zcwpw1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408769	M	MP:0000702	enlarged lymph nodes	Zcwpw1<em1(IMPC)Tcp>/Zcwpw1<em1(IMPC)Tcp>	C57BL/6N-Zcwpw1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408769	F	MP:0001944	abnormal pancreas morphology	Zcwpw1<em1(IMPC)Tcp>/Zcwpw1<em1(IMPC)Tcp>	C57BL/6N-Zcwpw1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408770	F	MP:0011965	decreased total retina thickness	Zdhhc5<tm1e.1(EUCOMM)Hmgu>/Zdhhc5<tm1e.1(EUCOMM)Hmgu>	C57BL/6NCrl-Zdhhc5<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408770	F	MP:0010511	shortened PR interval	Zdhhc5<tm1e.1(EUCOMM)Hmgu>/Zdhhc5<tm1e.1(EUCOMM)Hmgu>	C57BL/6NCrl-Zdhhc5<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408770	F	MP:0002792	abnormal retina vasculature morphology	Zdhhc5<tm1e.1(EUCOMM)Hmgu>/Zdhhc5<tm1e.1(EUCOMM)Hmgu>	C57BL/6NCrl-Zdhhc5<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408770	F	MP:0001325	abnormal retina morphology	Zdhhc5<tm1e.1(EUCOMM)Hmgu>/Zdhhc5<tm1e.1(EUCOMM)Hmgu>	C57BL/6NCrl-Zdhhc5<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408770	M	MP:0001489	decreased startle reflex	Zdhhc5<tm1e.1(EUCOMM)Hmgu>/Zdhhc5<tm1e.1(EUCOMM)Hmgu>	C57BL/6NCrl-Zdhhc5<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408770	M	MP:0008528	polycystic kidney	Zdhhc5<tm1e.1(EUCOMM)Hmgu>/Zdhhc5<tm1e.1(EUCOMM)Hmgu>	C57BL/6NCrl-Zdhhc5<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6408771	M	MP:0000186	decreased circulating HDL cholesterol level	Zfand6<em1(IMPC)Mbp>/Zfand6<em1(IMPC)Mbp>	C57BL/6N-Zfand6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408771	F	MP:0005344	increased circulating bilirubin level	Zfand6<em1(IMPC)Mbp>/Zfand6<em1(IMPC)Mbp>	C57BL/6N-Zfand6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408771	M	MP:0005179	decreased circulating cholesterol level	Zfand6<em1(IMPC)Mbp>/Zfand6<em1(IMPC)Mbp>	C57BL/6N-Zfand6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408771	F	MP:0005419	decreased circulating serum albumin level	Zfand6<em1(IMPC)Mbp>/Zfand6<em1(IMPC)Mbp>	C57BL/6N-Zfand6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408771	M	MP:0000691	enlarged spleen	Zfand6<em1(IMPC)Mbp>/Zfand6<em1(IMPC)Mbp>	C57BL/6N-Zfand6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408771	M	MP:0001147	small testis	Zfand6<em1(IMPC)Mbp>/Zfand6<em1(IMPC)Mbp>	C57BL/6N-Zfand6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408771	M	MP:0005567	decreased circulating total protein level	Zfand6<em1(IMPC)Mbp>/Zfand6<em1(IMPC)Mbp>	C57BL/6N-Zfand6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408771	M	MP:0000689	abnormal spleen morphology	Zfand6<em1(IMPC)Mbp>/Zfand6<em1(IMPC)Mbp>	C57BL/6N-Zfand6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408771	M	MP:0002135	abnormal kidney morphology	Zfand6<em1(IMPC)Mbp>/Zfand6<em1(IMPC)Mbp>	C57BL/6N-Zfand6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408771	M	MP:0001146	abnormal testis morphology	Zfand6<em1(IMPC)Mbp>/Zfand6<em1(IMPC)Mbp>	C57BL/6N-Zfand6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408771	M	MP:0000702	enlarged lymph nodes	Zfand6<em1(IMPC)Mbp>/Zfand6<em1(IMPC)Mbp>	C57BL/6N-Zfand6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408771	M	MP:0003068	enlarged kidney	Zfand6<em1(IMPC)Mbp>/Zfand6<em1(IMPC)Mbp>	C57BL/6N-Zfand6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408771	M	MP:0002339	abnormal lymph node morphology	Zfand6<em1(IMPC)Mbp>/Zfand6<em1(IMPC)Mbp>	C57BL/6N-Zfand6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6408772	F	MP:0003731	abnormal retina outer nuclear layer morphology	Zfp160<tm1b(EUCOMM)Wtsi>/Zfp160<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp160<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408772	M	MP:0004953	decreased spleen weight	Zfp160<tm1b(EUCOMM)Wtsi>/Zfp160<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp160<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408772	M	MP:0011110	preweaning lethality, incomplete penetrance	Zfp160<tm1b(EUCOMM)Wtsi>/Zfp160<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp160<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408772	M	MP:0010124	decreased bone mineral content	Zfp160<tm1b(EUCOMM)Wtsi>/Zfp160<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp160<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408772	M	MP:0000063	decreased bone mineral density	Zfp160<tm1b(EUCOMM)Wtsi>/Zfp160<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp160<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408774	F	MP:0001258	decreased body length	Zfp383<em1(IMPC)Wtsi>/Zfp383<em1(IMPC)Wtsi>	C57BL/6N-Zfp383<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408774	M	MP:0002941	increased circulating alanine transaminase level	Zfp383<em1(IMPC)Wtsi>/Zfp383<em1(IMPC)Wtsi>	C57BL/6N-Zfp383<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408775	M	MP:0003961	decreased lean body mass	Zfp629<em1(IMPC)Tcp>/Zfp629<em1(IMPC)Tcp>	C57BL/6N-Zfp629<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408775	M	MP:0010024	increased total body fat amount	Zfp629<em1(IMPC)Tcp>/Zfp629<em1(IMPC)Tcp>	C57BL/6N-Zfp629<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408775	M	MP:0001488	increased startle reflex	Zfp629<em1(IMPC)Tcp>/Zfp629<em1(IMPC)Tcp>	C57BL/6N-Zfp629<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408775	M	MP:0000692	small spleen	Zfp629<em1(IMPC)Tcp>/Zfp629<em1(IMPC)Tcp>	C57BL/6N-Zfp629<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408776	F	MP:0001554	increased circulating free fatty acids level	Zfp637<em1(IMPC)Wtsi>/Zfp637<em1(IMPC)Wtsi>	C57BL/6N-Zfp637<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408776	F	MP:0002599	increased mean platelet volume	Zfp637<em1(IMPC)Wtsi>/Zfp637<em1(IMPC)Wtsi>	C57BL/6N-Zfp637<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6408777	M	MP:0003179	thrombocytopenia	Zfp804a<em1(IMPC)Tcp>/Zfp804a<em1(IMPC)Tcp>	C57BL/6N-Zfp804a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408777	F	MP:0009709	hydrometra	Zfp804a<em1(IMPC)Tcp>/Zfp804a<em1(IMPC)Tcp>	C57BL/6N-Zfp804a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408777	M	MP:0003233	prolonged QT interval	Zfp804a<em1(IMPC)Tcp>/Zfp804a<em1(IMPC)Tcp>	C57BL/6N-Zfp804a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408777	F	MP:0002590	increased mean corpuscular volume	Zfp804a<em1(IMPC)Tcp>/Zfp804a<em1(IMPC)Tcp>	C57BL/6N-Zfp804a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408778	F	MP:0001488	increased startle reflex	Zfp91<em1(IMPC)Tcp>/Zfp91<+>	C57BL/6N-Zfp91<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408778	F	MP:0000702	enlarged lymph nodes	Zfp91<em1(IMPC)Tcp>/Zfp91<+>	C57BL/6N-Zfp91<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408778	M	MP:0001258	decreased body length	Zfp91<em1(IMPC)Tcp>/Zfp91<+>	C57BL/6N-Zfp91<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6408780	M	MP:0001289	persistence of hyaloid vascular system	Zfp930<tm1b(KOMP)Wtsi>/Zfp930<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp930<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408780	M	MP:0008259	abnormal optic disk morphology	Zfp930<tm1b(KOMP)Wtsi>/Zfp930<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp930<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6408780	F	MP:0011960	abnormal eye anterior chamber depth	Zfp930<tm1b(KOMP)Wtsi>/Zfp930<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp930<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6415589	M	MP:0011698	abnormal brown adipose tissue physiology	Tg(Adipoq-Zc3h10)#Hsul/0	Not Specified	N	31775033
MGI:6415589	M	MP:0020523	decreased susceptibility to induced hypothermia	Tg(Adipoq-Zc3h10)#Hsul/0	Not Specified	N	31775033
MGI:6415589	M	MP:0005289	increased oxygen consumption	Tg(Adipoq-Zc3h10)#Hsul/0	Not Specified	N	31775033
MGI:6415589	M	MP:0002891	increased insulin sensitivity	Tg(Adipoq-Zc3h10)#Hsul/0	Not Specified	N	31775033
MGI:6415589	M	MP:0005670	abnormal white adipose tissue physiology	Tg(Adipoq-Zc3h10)#Hsul/0	Not Specified	N	31775033
MGI:6415589	M	MP:0005292	improved glucose tolerance	Tg(Adipoq-Zc3h10)#Hsul/0	Not Specified	N	31775033
MGI:6415589	M	MP:0005659	decreased susceptibility to diet-induced obesity	Tg(Adipoq-Zc3h10)#Hsul/0	Not Specified	N	31775033
MGI:6415589	M	MP:0009116	abnormal brown fat cell morphology	Tg(Adipoq-Zc3h10)#Hsul/0	Not Specified	N	31775033
MGI:6415589	M	MP:0011699	abnormal brown adipose tissue thermogenesis	Tg(Adipoq-Zc3h10)#Hsul/0	Not Specified	N	31775033
MGI:6415589	M	MP:0011628	increased mitochondrial number	Tg(Adipoq-Zc3h10)#Hsul/0	Not Specified	N	31775033
MGI:6415591	M	MP:0011628	increased mitochondrial number	Tg(Adipoq-Zc3h10*)#Hsul/0	Not Specified	N	31775033
MGI:6415591	M	MP:0009116	abnormal brown fat cell morphology	Tg(Adipoq-Zc3h10*)#Hsul/0	Not Specified	N	31775033
MGI:6415591	M	MP:0011699	abnormal brown adipose tissue thermogenesis	Tg(Adipoq-Zc3h10*)#Hsul/0	Not Specified	N	31775033
MGI:6415591	M	MP:0005289	increased oxygen consumption	Tg(Adipoq-Zc3h10*)#Hsul/0	Not Specified	N	31775033
MGI:6415592	M	MP:0014142	increased body fat mass	Tg(Ucp1-cre)1Evdr/0,Zc3h10<tm1c(EUCOMM)Wtsi>/Zc3h10<tm1c(EUCOMM)Wtsi>	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	31775033
MGI:6415592	M	MP:0005331	insulin resistance	Tg(Ucp1-cre)1Evdr/0,Zc3h10<tm1c(EUCOMM)Wtsi>/Zc3h10<tm1c(EUCOMM)Wtsi>	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	31775033
MGI:6415592	M	MP:0005290	decreased oxygen consumption	Tg(Ucp1-cre)1Evdr/0,Zc3h10<tm1c(EUCOMM)Wtsi>/Zc3h10<tm1c(EUCOMM)Wtsi>	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	31775033
MGI:6415592	M	MP:0011049	impaired adaptive thermogenesis	Tg(Ucp1-cre)1Evdr/0,Zc3h10<tm1c(EUCOMM)Wtsi>/Zc3h10<tm1c(EUCOMM)Wtsi>	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	31775033
MGI:6415592	M	MP:0005293	impaired glucose tolerance	Tg(Ucp1-cre)1Evdr/0,Zc3h10<tm1c(EUCOMM)Wtsi>/Zc3h10<tm1c(EUCOMM)Wtsi>	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	31775033
MGI:6415592	M	MP:0011699	abnormal brown adipose tissue thermogenesis	Tg(Ucp1-cre)1Evdr/0,Zc3h10<tm1c(EUCOMM)Wtsi>/Zc3h10<tm1c(EUCOMM)Wtsi>	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	31775033
MGI:6415592	M	MP:0001260	increased body weight	Tg(Ucp1-cre)1Evdr/0,Zc3h10<tm1c(EUCOMM)Wtsi>/Zc3h10<tm1c(EUCOMM)Wtsi>	involves: 129S4/SvJaeSor * C57BL/6N * FVB	N	31775033
MGI:6416132	M	MP:0005389	reproductive system phenotype	Fgfr2<tm3.1Lni>/Fgfr2<+>,Hmgcs2<em1Wilh>/Hmgcs2<em1Wilh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	Y	31910233
MGI:6416161	M	MP:0000242	impaired fertilization	Pithd1<tm1Ohi>/Pithd1<tm1Ohi>	involves: C57BL/6N	N	31915251
MGI:6416161	M	MP:0001925	male infertility	Pithd1<tm1Ohi>/Pithd1<tm1Ohi>	involves: C57BL/6N	N	31915251
MGI:6416161	M	MP:0004884	abnormal testis physiology	Pithd1<tm1Ohi>/Pithd1<tm1Ohi>	involves: C57BL/6N	N	31915251
MGI:6416161	M	MP:0002675	asthenozoospermia	Pithd1<tm1Ohi>/Pithd1<tm1Ohi>	involves: C57BL/6N	N	31915251
MGI:6416161	M	MP:0031408	multi-headed sperm	Pithd1<tm1Ohi>/Pithd1<tm1Ohi>	involves: C57BL/6N	N	31915251
MGI:6416161	M	MP:0005578	teratozoospermia	Pithd1<tm1Ohi>/Pithd1<tm1Ohi>	involves: C57BL/6N	N	31915251
MGI:6416162	M	MP:0031408	multi-headed sperm	Pithd1<em1Osb>/Pithd1<em1Osb>	involves: C57BL/6 * DBA/2	N	31915251
MGI:6416162	M	MP:0000242	impaired fertilization	Pithd1<em1Osb>/Pithd1<em1Osb>	involves: C57BL/6 * DBA/2	N	31915251
MGI:6416162	M	MP:0005578	teratozoospermia	Pithd1<em1Osb>/Pithd1<em1Osb>	involves: C57BL/6 * DBA/2	N	31915251
MGI:6416162	M	MP:0002675	asthenozoospermia	Pithd1<em1Osb>/Pithd1<em1Osb>	involves: C57BL/6 * DBA/2	N	31915251
MGI:6416174	M	MP:0002675	asthenozoospermia	Hoatz<em1Seta>/Hoatz<em1Seta>	B6N.Cg-Hoatz<em1Seta>	N	32248064
MGI:6416174	M	MP:0005578	teratozoospermia	Hoatz<em1Seta>/Hoatz<em1Seta>	B6N.Cg-Hoatz<em1Seta>	N	32248064
MGI:6416174	M	MP:0009838	abnormal sperm axoneme morphology	Hoatz<em1Seta>/Hoatz<em1Seta>	B6N.Cg-Hoatz<em1Seta>	N	32248064
MGI:6416174	M	MP:0001925	male infertility	Hoatz<em1Seta>/Hoatz<em1Seta>	B6N.Cg-Hoatz<em1Seta>	N	32248064
MGI:6416174	M	MP:0006362	abnormal male germ cell morphology	Hoatz<em1Seta>/Hoatz<em1Seta>	B6N.Cg-Hoatz<em1Seta>	N	32248064
MGI:6416174	M	MP:0002687	oligozoospermia	Hoatz<em1Seta>/Hoatz<em1Seta>	B6N.Cg-Hoatz<em1Seta>	N	32248064
MGI:6416174	M	MP:0009239	short sperm flagellum	Hoatz<em1Seta>/Hoatz<em1Seta>	B6N.Cg-Hoatz<em1Seta>	N	32248064
MGI:6416174	M	MP:0008892	abnormal sperm flagellum morphology	Hoatz<em1Seta>/Hoatz<em1Seta>	B6N.Cg-Hoatz<em1Seta>	N	32248064
MGI:6416174	M	MP:0001147	small testis	Hoatz<em1Seta>/Hoatz<em1Seta>	B6N.Cg-Hoatz<em1Seta>	N	32248064
MGI:6416175	M	MP:0008892	abnormal sperm flagellum morphology	Hoatz<em1Seta>/Hoatz<+>	B6N.Cg-Hoatz<em1Seta>	N	32248064
MGI:6416175	F	MP:0008028	pregnancy-related premature death	Hoatz<em1Seta>/Hoatz<+>	B6N.Cg-Hoatz<em1Seta>	N	32248064
MGI:6416812	F	MP:0010052	increased grip strength	Slc22a17<em1(IMPC)H>/Slc22a17<+>	C57BL/6N-Slc22a17<em1(IMPC)H>/H	N	MGI:5576271
MGI:6423102	F	MP:0001262	decreased body weight	Muc4<tm1Unc>/Muc4<tm1Unc>	B6NTac.129(FVB)-Muc4<tm1Unc>/Rand	N	MGI:6416514
MGI:6423102	F	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality	Muc4<tm1Unc>/Muc4<tm1Unc>	B6NTac.129(FVB)-Muc4<tm1Unc>/Rand	N	MGI:6416514
MGI:6423102	F	MP:0001954	respiratory distress	Muc4<tm1Unc>/Muc4<tm1Unc>	B6NTac.129(FVB)-Muc4<tm1Unc>/Rand	N	MGI:6416514
MGI:6423102	F	MP:0020949	increased susceptibility to Coronaviridae infection	Muc4<tm1Unc>/Muc4<tm1Unc>	B6NTac.129(FVB)-Muc4<tm1Unc>/Rand	N	MGI:6416514
MGI:6430297	F	MP:0020216	decreased circulating complement protein level	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas	N	25891969
MGI:6430297	F	MP:0002743	glomerulonephritis	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas	N	25891969
MGI:6430297	F	MP:0004952	increased spleen weight	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas	N	25891969
MGI:6430297	F	MP:0009338	increased splenocyte number	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas	N	25891969
MGI:6430297	F	MP:0011353	expanded mesangial matrix	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas	N	25891969
MGI:6430297	F	MP:0011427	increased mesangial cell number	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas	N	25891969
MGI:6430297	F	MP:0005325	abnormal renal glomerulus morphology	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas	N	25891969
MGI:6430297	F	MP:0004801	increased susceptibility to systemic lupus erythematosus	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas	N	25891969
MGI:6430297	F	MP:0002871	albuminuria	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas	N	25891969
MGI:6430297	F	MP:0003917	increased kidney weight	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas	N	25891969
MGI:6430297	F	MP:0010219	increased T-helper 17 cell number	Bsg<tm1Tmu>/Bsg<tm1Tmu>	involves: 129S2/SvPas	N	25891969
MGI:6430622	M	MP:0011086	postnatal lethality, incomplete penetrance	Sh3rf2<tm1Zhxu>/Sh3rf2<tm1Zhxu>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430622	M	MP:0001732	postnatal growth retardation	Sh3rf2<tm1Zhxu>/Sh3rf2<tm1Zhxu>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430623	M	MP:0002574	increased vertical activity	Sh3rf2<tm1Zhxu>/Sh3rf2<+>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430623	M	MP:0002272	abnormal nervous system electrophysiology	Sh3rf2<tm1Zhxu>/Sh3rf2<+>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430623	M	MP:0003412	abnormal afterhyperpolarization	Sh3rf2<tm1Zhxu>/Sh3rf2<+>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430623	M	MP:0001409	increased stereotypic behavior	Sh3rf2<tm1Zhxu>/Sh3rf2<+>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430623	M	MP:0001360	abnormal social investigation	Sh3rf2<tm1Zhxu>/Sh3rf2<+>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430623	M	MP:0001447	abnormal nest building behavior	Sh3rf2<tm1Zhxu>/Sh3rf2<+>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430623	M	MP:0001732	postnatal growth retardation	Sh3rf2<tm1Zhxu>/Sh3rf2<+>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430623	M	MP:0004753	abnormal miniature excitatory postsynaptic currents	Sh3rf2<tm1Zhxu>/Sh3rf2<+>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430623	M	MP:0011086	postnatal lethality, incomplete penetrance	Sh3rf2<tm1Zhxu>/Sh3rf2<+>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430623	M	MP:0001399	hyperactivity	Sh3rf2<tm1Zhxu>/Sh3rf2<+>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430623	M	MP:0020395	abnormal response to social novelty	Sh3rf2<tm1Zhxu>/Sh3rf2<+>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430623	M	MP:0020351	decreased vocalization	Sh3rf2<tm1Zhxu>/Sh3rf2<+>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430623	M	MP:0002064	seizures	Sh3rf2<tm1Zhxu>/Sh3rf2<+>	C57BL/6-Sh3rf2<tm1Zhxu>	N	30540932
MGI:6430624	M	MP:0009936	abnormal dendritic spine morphology	Sh3rf2<tm1Zhxu>/Sh3rf2<+>,Tg(Thy1-EGFP)MJrs/0	involves: C57BL/6 * C57BL/6J * CBA	N	30540932
MGI:6430624	M	MP:0000807	abnormal hippocampus morphology	Sh3rf2<tm1Zhxu>/Sh3rf2<+>,Tg(Thy1-EGFP)MJrs/0	involves: C57BL/6 * C57BL/6J * CBA	N	30540932
MGI:6430624	M	MP:0020507	increased dendritic spine density	Sh3rf2<tm1Zhxu>/Sh3rf2<+>,Tg(Thy1-EGFP)MJrs/0	involves: C57BL/6 * C57BL/6J * CBA	N	30540932
MGI:6430624	M	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology	Sh3rf2<tm1Zhxu>/Sh3rf2<+>,Tg(Thy1-EGFP)MJrs/0	involves: C57BL/6 * C57BL/6J * CBA	N	30540932
MGI:6431340	F	MP:0010210	abnormal circulating cytokine level	Ace2<em1(ACE2)Yowa>/Ace2<em1(ACE2)Yowa>	C57BL/6-Ace2<em1(ACE2)Yowa>	N	32485164
MGI:6431340	F	MP:0001862	interstitial pneumonia	Ace2<em1(ACE2)Yowa>/Ace2<em1(ACE2)Yowa>	C57BL/6-Ace2<em1(ACE2)Yowa>	N	32485164
MGI:6431340	F	MP:0001182	lung hemorrhage	Ace2<em1(ACE2)Yowa>/Ace2<em1(ACE2)Yowa>	C57BL/6-Ace2<em1(ACE2)Yowa>	N	32485164
MGI:6431340	F	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology	Ace2<em1(ACE2)Yowa>/Ace2<em1(ACE2)Yowa>	C57BL/6-Ace2<em1(ACE2)Yowa>	N	32485164
MGI:6431340	F	MP:0020949	increased susceptibility to Coronaviridae infection	Ace2<em1(ACE2)Yowa>/Ace2<em1(ACE2)Yowa>	C57BL/6-Ace2<em1(ACE2)Yowa>	N	32485164
MGI:6431340	F	MP:0008577	increased circulating interferon-gamma level	Ace2<em1(ACE2)Yowa>/Ace2<em1(ACE2)Yowa>	C57BL/6-Ace2<em1(ACE2)Yowa>	N	32485164
MGI:6431340	F	MP:0008629	increased circulating interleukin-9 level	Ace2<em1(ACE2)Yowa>/Ace2<em1(ACE2)Yowa>	C57BL/6-Ace2<em1(ACE2)Yowa>	N	32485164
MGI:6431858	M	MP:0031356	abnormal outer dense fiber morphology	Cfap69<em1Fzh>/Cfap69<em1Fzh>	involves: C57BL/6J	N	30415212
MGI:6431858	M	MP:0001925	male infertility	Cfap69<em1Fzh>/Cfap69<em1Fzh>	involves: C57BL/6J	N	30415212
MGI:6431858	M	MP:0020869	immotile sperm	Cfap69<em1Fzh>/Cfap69<em1Fzh>	involves: C57BL/6J	N	30415212
MGI:6431858	M	MP:0008545	absent sperm flagellum	Cfap69<em1Fzh>/Cfap69<em1Fzh>	involves: C57BL/6J	N	30415212
MGI:6431858	M	MP:0009230	abnormal sperm head morphology	Cfap69<em1Fzh>/Cfap69<em1Fzh>	involves: C57BL/6J	N	30415212
MGI:6431858	M	MP:0009239	short sperm flagellum	Cfap69<em1Fzh>/Cfap69<em1Fzh>	involves: C57BL/6J	N	30415212
MGI:6431858	M	MP:0008892	abnormal sperm flagellum morphology	Cfap69<em1Fzh>/Cfap69<em1Fzh>	involves: C57BL/6J	N	30415212
MGI:6431858	M	MP:0009838	abnormal sperm axoneme morphology	Cfap69<em1Fzh>/Cfap69<em1Fzh>	involves: C57BL/6J	N	30415212
MGI:6431858	M	MP:0009238	coiled sperm flagellum	Cfap69<em1Fzh>/Cfap69<em1Fzh>	involves: C57BL/6J	N	30415212
MGI:6431858	M	MP:0008898	abnormal acrosome morphology	Cfap69<em1Fzh>/Cfap69<em1Fzh>	involves: C57BL/6J	N	30415212
MGI:6437396	M	MP:0001147	small testis	Tesmin<em1Osb>/Tesmin<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	31916570
MGI:6437396	M	MP:0001155	arrest of spermatogenesis	Tesmin<em1Osb>/Tesmin<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	31916570
MGI:6437396	M	MP:0001925	male infertility	Tesmin<em1Osb>/Tesmin<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	31916570
MGI:6437396	M	MP:0004852	decreased testis weight	Tesmin<em1Osb>/Tesmin<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	31916570
MGI:6437396	M	MP:0008261	arrest of male meiosis	Tesmin<em1Osb>/Tesmin<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	31916570
MGI:6437563	M	MP:0031010	failure of sperm-egg fusion	Tmem95<em1Osb>/Tmem95<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32393636
MGI:6437563	M	MP:0001925	male infertility	Tmem95<em1Osb>/Tmem95<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32393636
MGI:6437564	M	MP:0031010	failure of sperm-egg fusion	Spaca6<em2Osb>/Spaca6<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32393636
MGI:6437564	M	MP:0001925	male infertility	Spaca6<em2Osb>/Spaca6<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32393636
MGI:6437778	F	MP:0005542	cornea vascularization	Ace2<tm1Cof>/Ace2<tm1Cof>	involves: 129S6/SvEvTac * C57BL/6	N	32725927
MGI:6437778	F	MP:0001314	cornea opacity	Ace2<tm1Cof>/Ace2<tm1Cof>	involves: 129S6/SvEvTac * C57BL/6	N	32725927
MGI:6437778	F	MP:0020861	abnormal cornea wound healing	Ace2<tm1Cof>/Ace2<tm1Cof>	involves: 129S6/SvEvTac * C57BL/6	N	32725927
MGI:6437778	F	MP:0006000	abnormal cornea epithelium morphology	Ace2<tm1Cof>/Ace2<tm1Cof>	involves: 129S6/SvEvTac * C57BL/6	N	32725927
MGI:6437778	F	MP:0001313	increased incidence of corneal inflammation	Ace2<tm1Cof>/Ace2<tm1Cof>	involves: 129S6/SvEvTac * C57BL/6	N	32725927
MGI:6437833	M	MP:0001925	male infertility	Llcfc1<em2Osb>/Llcfc1<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	32393636
MGI:6437834	M	MP:0001925	male infertility	Llcfc1<em3Osb>/Llcfc1<em3Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	32393636
MGI:6437929	F	MP:0002757	decreased vertical activity	Shank3<tm2Cmpl>/Shank3<+>	B6.129S6-Shank3<tm2Cmpl>	N	27492494
MGI:6437929	F	MP:0001405	impaired coordination	Shank3<tm2Cmpl>/Shank3<+>	B6.129S6-Shank3<tm2Cmpl>	N	27492494
MGI:6437930	F	MP:0001405	impaired coordination	Shank3<tm2Cmpl>/Shank3<tm2Cmpl>	B6.129S6-Shank3<tm2Cmpl>	N	27492494
MGI:6437930	F	MP:0002757	decreased vertical activity	Shank3<tm2Cmpl>/Shank3<tm2Cmpl>	B6.129S6-Shank3<tm2Cmpl>	N	27492494
MGI:6438177	F	MP:0000752	dystrophic muscle	Dmd<em4Eno>/Dmd<em4Eno>	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438177	F	MP:0004510	myositis	Dmd<em4Eno>/Dmd<em4Eno>	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438177	F	MP:0010090	increased circulating creatine kinase level	Dmd<em4Eno>/Dmd<em4Eno>	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438177	F	MP:0010053	decreased grip strength	Dmd<em4Eno>/Dmd<em4Eno>	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438177	F	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<em4Eno>/Dmd<em4Eno>	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438177	F	MP:0009419	skeletal muscle fibrosis	Dmd<em4Eno>/Dmd<em4Eno>	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438177	F	MP:0009412	skeletal muscle fiber degeneration	Dmd<em4Eno>/Dmd<em4Eno>	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438177	F	MP:0000747	muscle weakness	Dmd<em4Eno>/Dmd<em4Eno>	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438180	M	MP:0010090	increased circulating creatine kinase level	Dmd<em4Eno>/Y	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438180	M	MP:0000747	muscle weakness	Dmd<em4Eno>/Y	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438180	M	MP:0009404	centrally nucleated skeletal muscle fibers	Dmd<em4Eno>/Y	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438180	M	MP:0009412	skeletal muscle fiber degeneration	Dmd<em4Eno>/Y	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438180	M	MP:0000752	dystrophic muscle	Dmd<em4Eno>/Y	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438180	M	MP:0009419	skeletal muscle fibrosis	Dmd<em4Eno>/Y	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438180	M	MP:0004510	myositis	Dmd<em4Eno>/Y	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438180	M	MP:0010053	decreased grip strength	Dmd<em4Eno>/Y	C57BL/6-Dmd<em4Eno>	N	30854433
MGI:6438267	F	MP:0001935	decreased litter size	Del(19Oosp2-Oosp3)2Osb/Del(19Oosp2-Oosp3)2Osb	involves: C57BL/6 * DBA/2	N	32231122
MGI:6438267	F	MP:0005389	reproductive system phenotype	Del(19Oosp2-Oosp3)2Osb/Del(19Oosp2-Oosp3)2Osb	involves: C57BL/6 * DBA/2	Y	32231122
MGI:6441077	F	MP:0011939	increased food intake	Hdac4<em1Hcu>/Hdac4<+>	involves: C57BL/6 * CBA	N	27884425
MGI:6441077	F	MP:0001363	increased anxiety-related response	Hdac4<em1Hcu>/Hdac4<+>	involves: C57BL/6 * CBA	N	27884425
MGI:6441077	F	MP:0005455	increased susceptibility to weight gain	Hdac4<em1Hcu>/Hdac4<+>	involves: C57BL/6 * CBA	N	27884425
MGI:6441077	F	MP:0001441	increased grooming behavior	Hdac4<em1Hcu>/Hdac4<+>	involves: C57BL/6 * CBA	N	27884425
MGI:6441077	F	MP:0001432	abnormal food preference	Hdac4<em1Hcu>/Hdac4<+>	involves: C57BL/6 * CBA	N	27884425
MGI:6441077	F	MP:0003063	increased coping response	Hdac4<em1Hcu>/Hdac4<+>	involves: C57BL/6 * CBA	N	27884425
MGI:6441077	F	MP:0002803	abnormal operant conditioning behavior	Hdac4<em1Hcu>/Hdac4<+>	involves: C57BL/6 * CBA	N	27884425
MGI:6441085	F	MP:0001441	increased grooming behavior	Hdac4<em1Hcu>/Hdac4<em1Hcu>	involves: 129 * C57BL/6 * CBA	N	32153359
MGI:6441085	M	MP:0011940	decreased food intake	Hdac4<em1Hcu>/Hdac4<em1Hcu>	involves: 129 * C57BL/6 * CBA	N	32153359
MGI:6441085	F	MP:0003863	decreased aggression towards mice	Hdac4<em1Hcu>/Hdac4<em1Hcu>	involves: 129 * C57BL/6 * CBA	N	32153359
MGI:6441085	M	MP:0002757	decreased vertical activity	Hdac4<em1Hcu>/Hdac4<em1Hcu>	involves: 129 * C57BL/6 * CBA	N	32153359
MGI:6441085	M	MP:0001402	decreased locomotor activity	Hdac4<em1Hcu>/Hdac4<em1Hcu>	involves: 129 * C57BL/6 * CBA	N	32153359
MGI:6441085	M	MP:0010182	decreased susceptibility to weight gain	Hdac4<em1Hcu>/Hdac4<em1Hcu>	involves: 129 * C57BL/6 * CBA	N	32153359
MGI:6441085	M	MP:0001363	increased anxiety-related response	Hdac4<em1Hcu>/Hdac4<em1Hcu>	involves: 129 * C57BL/6 * CBA	N	32153359
MGI:6441085	M	MP:0002803	abnormal operant conditioning behavior	Hdac4<em1Hcu>/Hdac4<em1Hcu>	involves: 129 * C57BL/6 * CBA	N	32153359
MGI:6442585	M	MP:0001406	abnormal gait	Kmt2d<bapa>/Kmt2d<bapa>	BALB/cJ-Kmt2d<bapa>	N	30891914
MGI:6442585	M	MP:0001407	short stride length	Kmt2d<bapa>/Kmt2d<bapa>	BALB/cJ-Kmt2d<bapa>	N	30891914
MGI:6442585	M	MP:0001485	abnormal pinna reflex	Kmt2d<bapa>/Kmt2d<bapa>	BALB/cJ-Kmt2d<bapa>	N	30891914
MGI:6442585	M	MP:0002066	abnormal motor capabilities/coordination/movement	Kmt2d<bapa>/Kmt2d<bapa>	BALB/cJ-Kmt2d<bapa>	N	30891914
MGI:6442585	F	MP:0005498	hyporesponsive to tactile stimuli	Kmt2d<bapa>/Kmt2d<bapa>	BALB/cJ-Kmt2d<bapa>	N	30891914
MGI:6444812	M	MP:0004720	abnormal platelet morphology	Coro1c<tm1d(KOMP)Wtsi>/Coro1c<tm1d(KOMP)Wtsi>	involves: C57BL/6N	N	31677819
MGI:6444812	M	MP:0005505	thrombocytosis	Coro1c<tm1d(KOMP)Wtsi>/Coro1c<tm1d(KOMP)Wtsi>	involves: C57BL/6N	N	31677819
MGI:6444812	M	MP:0002968	increased circulating alkaline phosphatase level	Coro1c<tm1d(KOMP)Wtsi>/Coro1c<tm1d(KOMP)Wtsi>	involves: C57BL/6N	N	31677819
MGI:6446187	F	MP:0002681	increased corpora lutea number	Mir505<em1Xhj>/Mir505<em1Xhj>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446187	F	MP:0001750	increased circulating follicle stimulating hormone level	Mir505<em1Xhj>/Mir505<em1Xhj>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446187	F	MP:0003378	early sexual maturation	Mir505<em1Xhj>/Mir505<em1Xhj>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446187	F	MP:0004855	increased ovary weight	Mir505<em1Xhj>/Mir505<em1Xhj>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446187	F	MP:0004514	dystocia	Mir505<em1Xhj>/Mir505<em1Xhj>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446187	F	MP:0004904	increased uterus weight	Mir505<em1Xhj>/Mir505<em1Xhj>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446187	F	MP:0001934	increased litter size	Mir505<em1Xhj>/Mir505<em1Xhj>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446187	F	MP:0001262	decreased body weight	Mir505<em1Xhj>/Mir505<em1Xhj>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446187	F	MP:0002865	increased growth rate	Mir505<em1Xhj>/Mir505<em1Xhj>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446187	F	MP:0001751	increased circulating luteinizing hormone level	Mir505<em1Xhj>/Mir505<em1Xhj>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446187	F	MP:0008994	early vaginal opening	Mir505<em1Xhj>/Mir505<em1Xhj>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446187	F	MP:0001260	increased body weight	Mir505<em1Xhj>/Mir505<em1Xhj>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446192	F	MP:0003378	early sexual maturation	Mir505<em1Xhj>/Mir505<+>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446192	F	MP:0008994	early vaginal opening	Mir505<em1Xhj>/Mir505<+>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446192	F	MP:0001262	decreased body weight	Mir505<em1Xhj>/Mir505<+>	C57BL/6J-Mir505<em1Xhj>	N	30557853
MGI:6446899	F	MP:0009397	increased trophoblast giant cell number	Gab3<em1Khoe>/Gab3<em1Khoe>	C57BL/6-Gab3<em1Khoe>	N	31375526
MGI:6446899	F	MP:0008054	abnormal uterine NK cell morphology	Gab3<em1Khoe>/Gab3<em1Khoe>	C57BL/6-Gab3<em1Khoe>	N	31375526
MGI:6446899	F	MP:0004514	dystocia	Gab3<em1Khoe>/Gab3<em1Khoe>	C57BL/6-Gab3<em1Khoe>	N	31375526
MGI:6446901	F	MP:0009397	increased trophoblast giant cell number	Gab3<m1Khoe>/Gab3<m1Khoe>	C57BL/6-Gab3<m1Khoe>	N	31375526
MGI:6446901	F	MP:0008054	abnormal uterine NK cell morphology	Gab3<m1Khoe>/Gab3<m1Khoe>	C57BL/6-Gab3<m1Khoe>	N	31375526
MGI:6446901	F	MP:0004514	dystocia	Gab3<m1Khoe>/Gab3<m1Khoe>	C57BL/6-Gab3<m1Khoe>	N	31375526
MGI:6448103	F	MP:0020099	increased susceptibility to diet-induced aortic fatty streak lesions	Ldlr<tm1Her>/Ldlr<tm1Her>,Pla2g12a<rs36523879-C>/Pla2g12a<rs36523879-C>	FVB.Cg-Pla2g12a<rs36523879-C> Ldlr<tm1Her>	N	28917158
MGI:6448132	M	MP:0001922	reduced male fertility	Del(2Svs2-Svs5)1Natka/Del(2Svs2-Svs5)1Natka	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * DBA/1	N	31540031
MGI:6448132	M	MP:0005389	reproductive system phenotype	Del(2Svs2-Svs5)1Natka/Del(2Svs2-Svs5)1Natka	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * DBA/1	Y	31540031
MGI:6448132	M	MP:0030983	failure of copulatory plug deposition	Del(2Svs2-Svs5)1Natka/Del(2Svs2-Svs5)1Natka	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * DBA/1	N	31540031
MGI:6448362	M	MP:0006308	enlarged seminiferous tubules	Ddb1<tm1Spg>/Ddb1<tm1Spg>,Plekha5<Tg(AMH-cre)1Flor>/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	31779270
MGI:6448362	M	MP:0002216	abnormal seminiferous tubule morphology	Ddb1<tm1Spg>/Ddb1<tm1Spg>,Plekha5<Tg(AMH-cre)1Flor>/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	31779270
MGI:6448362	M	MP:0002687	oligozoospermia	Ddb1<tm1Spg>/Ddb1<tm1Spg>,Plekha5<Tg(AMH-cre)1Flor>/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	31779270
MGI:6448362	M	MP:0006428	ectopic Sertoli cells	Ddb1<tm1Spg>/Ddb1<tm1Spg>,Plekha5<Tg(AMH-cre)1Flor>/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	31779270
MGI:6448362	M	MP:0001147	small testis	Ddb1<tm1Spg>/Ddb1<tm1Spg>,Plekha5<Tg(AMH-cre)1Flor>/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	31779270
MGI:6448362	M	MP:0006418	abnormal testis cord formation	Ddb1<tm1Spg>/Ddb1<tm1Spg>,Plekha5<Tg(AMH-cre)1Flor>/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	31779270
MGI:6448362	M	MP:0005250	decreased Sertoli cell number	Ddb1<tm1Spg>/Ddb1<tm1Spg>,Plekha5<Tg(AMH-cre)1Flor>/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	31779270
MGI:6449004	F	MP:0001876	decreased inflammatory response	Ly6e<tm1c(EUCOMM)Hmgu>/Ly6e<tm1c(EUCOMM)Hmgu>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	B6.Cg-Ly6e<tm1c(EUCOMM)Hmgu> Commd10<Tg(Vav1-icre)A2Kio>	N	32704094
MGI:6449004	F	MP:0002941	increased circulating alanine transaminase level	Ly6e<tm1c(EUCOMM)Hmgu>/Ly6e<tm1c(EUCOMM)Hmgu>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	B6.Cg-Ly6e<tm1c(EUCOMM)Hmgu> Commd10<Tg(Vav1-icre)A2Kio>	N	32704094
MGI:6449004	F	MP:0001654	hepatic necrosis	Ly6e<tm1c(EUCOMM)Hmgu>/Ly6e<tm1c(EUCOMM)Hmgu>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	B6.Cg-Ly6e<tm1c(EUCOMM)Hmgu> Commd10<Tg(Vav1-icre)A2Kio>	N	32704094
MGI:6449004	F	MP:0008247	abnormal mononuclear cell morphology	Ly6e<tm1c(EUCOMM)Hmgu>/Ly6e<tm1c(EUCOMM)Hmgu>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	B6.Cg-Ly6e<tm1c(EUCOMM)Hmgu> Commd10<Tg(Vav1-icre)A2Kio>	N	32704094
MGI:6449004	F	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Ly6e<tm1c(EUCOMM)Hmgu>/Ly6e<tm1c(EUCOMM)Hmgu>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	B6.Cg-Ly6e<tm1c(EUCOMM)Hmgu> Commd10<Tg(Vav1-icre)A2Kio>	N	32704094
MGI:6449004	M	MP:0008127	decreased dendritic cell number	Ly6e<tm1c(EUCOMM)Hmgu>/Ly6e<tm1c(EUCOMM)Hmgu>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	B6.Cg-Ly6e<tm1c(EUCOMM)Hmgu> Commd10<Tg(Vav1-icre)A2Kio>	N	32704094
MGI:6449004	M	MP:0000222	decreased neutrophil cell number	Ly6e<tm1c(EUCOMM)Hmgu>/Ly6e<tm1c(EUCOMM)Hmgu>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	B6.Cg-Ly6e<tm1c(EUCOMM)Hmgu> Commd10<Tg(Vav1-icre)A2Kio>	N	32704094
MGI:6449004	F	MP:0000598	abnormal liver morphology	Ly6e<tm1c(EUCOMM)Hmgu>/Ly6e<tm1c(EUCOMM)Hmgu>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	B6.Cg-Ly6e<tm1c(EUCOMM)Hmgu> Commd10<Tg(Vav1-icre)A2Kio>	N	32704094
MGI:6449004	M	MP:0003884	decreased macrophage cell number	Ly6e<tm1c(EUCOMM)Hmgu>/Ly6e<tm1c(EUCOMM)Hmgu>,Commd10<Tg(Vav1-icre)A2Kio>/Commd10<+>	B6.Cg-Ly6e<tm1c(EUCOMM)Hmgu> Commd10<Tg(Vav1-icre)A2Kio>	N	32704094
MGI:6449146	F	MP:0001861	lung inflammation	Ace2<tm1a(KOMP)Wtsi>/Ace2<tm1a(KOMP)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C57BL/6N * C57BL/6NTac	N	31645418
MGI:6449146	F	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality	Ace2<tm1a(KOMP)Wtsi>/Ace2<tm1a(KOMP)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C57BL/6N * C57BL/6NTac	N	31645418
MGI:6449146	F	MP:0010180	increased susceptibility to weight loss	Ace2<tm1a(KOMP)Wtsi>/Ace2<tm1a(KOMP)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C57BL/6N * C57BL/6NTac	N	31645418
MGI:6449146	F	MP:0002412	increased susceptibility to bacterial infection	Ace2<tm1a(KOMP)Wtsi>/Ace2<tm1a(KOMP)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C57BL/6N * C57BL/6NTac	N	31645418
MGI:6449146	F	MP:0000219	increased neutrophil cell number	Ace2<tm1a(KOMP)Wtsi>/Ace2<tm1a(KOMP)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C57BL/6N * C57BL/6NTac	N	31645418
MGI:6449147	M	MP:0002412	increased susceptibility to bacterial infection	Ace2<tm1a(KOMP)Wtsi>/Y,Tg(FOXJ1-cre)F26Htzm/0	involves: C57BL/6N * C57BL/6NTac	N	31645418
MGI:6449147	M	MP:0001861	lung inflammation	Ace2<tm1a(KOMP)Wtsi>/Y,Tg(FOXJ1-cre)F26Htzm/0	involves: C57BL/6N * C57BL/6NTac	N	31645418
MGI:6449147	M	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality	Ace2<tm1a(KOMP)Wtsi>/Y,Tg(FOXJ1-cre)F26Htzm/0	involves: C57BL/6N * C57BL/6NTac	N	31645418
MGI:6449147	M	MP:0000219	increased neutrophil cell number	Ace2<tm1a(KOMP)Wtsi>/Y,Tg(FOXJ1-cre)F26Htzm/0	involves: C57BL/6N * C57BL/6NTac	N	31645418
MGI:6449147	M	MP:0010180	increased susceptibility to weight loss	Ace2<tm1a(KOMP)Wtsi>/Y,Tg(FOXJ1-cre)F26Htzm/0	involves: C57BL/6N * C57BL/6NTac	N	31645418
MGI:6449260	M	MP:0001273	decreased metastatic potential	Tg(TRAMP)8247Ng/0,Tmprss2<tm1Psn>/Tmprss2<tm1Psn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25122198
MGI:6449260	M	MP:0003721	increased tumor growth/size	Tg(TRAMP)8247Ng/0,Tmprss2<tm1Psn>/Tmprss2<tm1Psn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	25122198
MGI:6450214	M	MP:0005376	homeostasis/metabolism phenotype	Apoe<tm3(APOE_i3)Sfu>/Apoe<tm3(APOE_i3)Sfu>,Tg(APPSWE)2576Kha/0	involves: C57BL/6 * C57BL/6N * SJL	Y	17472586
MGI:6450215	M	MP:0005376	homeostasis/metabolism phenotype	Apoe<tm1(APOE_i4)Sfu>/Apoe<tm1(APOE_i4)Sfu>,Tg(APPSWE)2576Kha/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N * SJL	Y	17472586
MGI:6451096	M	MP:0009838	abnormal sperm axoneme morphology	Cfap65<em1Fzh>/Cfap65<em1Fzh>	involves: C57BL/6	N	31501240
MGI:6451096	M	MP:0031352	absent sperm axonemal central pair	Cfap65<em1Fzh>/Cfap65<em1Fzh>	involves: C57BL/6	N	31501240
MGI:6451096	M	MP:0014052	increased male germ cell apoptosis	Cfap65<em1Fzh>/Cfap65<em1Fzh>	involves: C57BL/6	N	31501240
MGI:6451096	M	MP:0001925	male infertility	Cfap65<em1Fzh>/Cfap65<em1Fzh>	involves: C57BL/6	N	31501240
MGI:6451096	M	MP:0008545	absent sperm flagellum	Cfap65<em1Fzh>/Cfap65<em1Fzh>	involves: C57BL/6	N	31501240
MGI:6451096	M	MP:0009238	coiled sperm flagellum	Cfap65<em1Fzh>/Cfap65<em1Fzh>	involves: C57BL/6	N	31501240
MGI:6451096	M	MP:0009239	short sperm flagellum	Cfap65<em1Fzh>/Cfap65<em1Fzh>	involves: C57BL/6	N	31501240
MGI:6451400	F	MP:0005390	skeleton phenotype	Tg(Ddx4-cre)1Dcas/0,Rnf220<em1Kust>/Rnf220<em1Kust>	involves: C57BL/6 * FVB	N	31291587
MGI:6451400	F	MP:0000939	decreased motor neuron number	Tg(Ddx4-cre)1Dcas/0,Rnf220<em1Kust>/Rnf220<em1Kust>	involves: C57BL/6 * FVB	N	31291587
MGI:6451400	F	MP:0011087	neonatal lethality, complete penetrance	Tg(Ddx4-cre)1Dcas/0,Rnf220<em1Kust>/Rnf220<em1Kust>	involves: C57BL/6 * FVB	N	31291587
MGI:6451400	F	MP:0002151	abnormal neural tube morphology	Tg(Ddx4-cre)1Dcas/0,Rnf220<em1Kust>/Rnf220<em1Kust>	involves: C57BL/6 * FVB	N	31291587
MGI:6451401	F	MP:0003491	abnormal voluntary movement	Rnf220<em1.1Kust>/Rnf220<+>	involves: C57BL/6	N	31291587
MGI:6451401	F	MP:0002083	premature death	Rnf220<em1.1Kust>/Rnf220<+>	involves: C57BL/6	N	31291587
MGI:6451401	F	MP:0000753	paralysis	Rnf220<em1.1Kust>/Rnf220<+>	involves: C57BL/6	N	31291587
MGI:6452491	M	MP:0014383	decreased miniature inhibitory postsynaptic current frequency	Zdhhc7<tm1.1Wqz>/Zdhhc7<tm1.1Wqz>	involves: 129S/Sv * C57BL/6J	N	31183559
MGI:6452491	F	MP:0014384	increased miniature inhibitory postsynaptic current amplitude	Zdhhc7<tm1.1Wqz>/Zdhhc7<tm1.1Wqz>	involves: 129S/Sv * C57BL/6J	N	31183559
MGI:6452491	M	MP:0011270	decreased excitatory postsynaptic current amplitude	Zdhhc7<tm1.1Wqz>/Zdhhc7<tm1.1Wqz>	involves: 129S/Sv * C57BL/6J	N	31183559
MGI:6452491	F	MP:0020870	decreased thigmotaxis	Zdhhc7<tm1.1Wqz>/Zdhhc7<tm1.1Wqz>	involves: 129S/Sv * C57BL/6J	N	31183559
MGI:6452491	F	MP:0001364	decreased anxiety-related response	Zdhhc7<tm1.1Wqz>/Zdhhc7<tm1.1Wqz>	involves: 129S/Sv * C57BL/6J	N	31183559
MGI:6452491	F	MP:0031391	increased locomotor activity	Zdhhc7<tm1.1Wqz>/Zdhhc7<tm1.1Wqz>	involves: 129S/Sv * C57BL/6J	N	31183559
MGI:6452491	F	MP:0008428	abnormal spatial working memory	Zdhhc7<tm1.1Wqz>/Zdhhc7<tm1.1Wqz>	involves: 129S/Sv * C57BL/6J	N	31183559
MGI:6452826	M	MP:0020852	abnormal olfactory behavior	Or5an6<tm2.1(tauEGFP)Hsak>/Or5an6<tm2.1(tauEGFP)Hsak>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	30643144
MGI:6452828	F	MP:0020852	abnormal olfactory behavior	Or10ad1c<tm1.1Hsak>/Or10ad1c<tm1.1Hsak>	C57BL/6-Or10ad1c<tm1.1Hsak>	N	30643144
MGI:6452965	F	MP:0004896	abnormal endometrium morphology	Fau<tm1.1Smoc>/Fau<+>	involves: 129 * C57BL/6J * FVB/N	N	26031240
MGI:6452965	F	MP:0003718	maternal effect	Fau<tm1.1Smoc>/Fau<+>	involves: 129 * C57BL/6J * FVB/N	N	26031240
MGI:6452965	F	MP:0001935	decreased litter size	Fau<tm1.1Smoc>/Fau<+>	involves: 129 * C57BL/6J * FVB/N	N	26031240
MGI:6452970	M	MP:0002790	decreased circulating follicle stimulating hormone level	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	F	MP:0009017	prolonged estrus	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	F	MP:0009047	short metestrus	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	M	MP:0004910	decreased seminal vesicle weight	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	F	MP:0009015	short proestrus	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	F	MP:0008869	anovulation	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	F	MP:0002680	decreased corpora lutea number	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	F	MP:0001127	small ovary	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	M	MP:0031436	decreased copulatory plug deposition	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	F	MP:0004856	decreased ovary weight	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	F	MP:0009006	prolonged estrous cycle	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	F	MP:0009444	ovarian follicular cyst	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	F	MP:0001923	reduced female fertility	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	M	MP:0001922	reduced male fertility	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	F	MP:0008948	decreased neuron number	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6452970	M	MP:0005389	reproductive system phenotype	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	Y	21228153
MGI:6452970	F	MP:0001126	abnormal ovary morphology	Six6<tm1Rsd>/Six6<tm1Rsd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	21228153
MGI:6454004	M	MP:0006380	abnormal spermatid morphology	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454004	M	MP:0002687	oligozoospermia	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454004	M	MP:0009230	abnormal sperm head morphology	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454004	M	MP:0004852	decreased testis weight	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454004	M	MP:0020451	decreased sperm progressive motility	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454004	M	MP:0008892	abnormal sperm flagellum morphology	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454004	M	MP:0001922	reduced male fertility	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454004	M	MP:0009282	decreased hyperactivated sperm motility	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454004	M	MP:0001932	abnormal spermiogenesis	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454004	M	MP:0009831	abnormal sperm midpiece morphology	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454004	M	MP:0008898	abnormal acrosome morphology	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454004	M	MP:0001260	increased body weight	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454004	M	MP:0009234	absent sperm head	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454004	M	MP:0001935	decreased litter size	Fam170a<em1Osb>/Fam170a<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454005	M	MP:0005389	reproductive system phenotype	Fam170b<em2Osb>/Fam170b<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	32588889
MGI:6454006	M	MP:0001935	decreased litter size	Fam170a<em1Osb>/Fam170a<em1Osb>,Fam170b<em2Osb>/Fam170b<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454006	M	MP:0001922	reduced male fertility	Fam170a<em1Osb>/Fam170a<em1Osb>,Fam170b<em2Osb>/Fam170b<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588889
MGI:6454993	M	MP:0005389	reproductive system phenotype	Prss51<em1Osb>/Prss51<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	32301961
MGI:6454994	M	MP:0009647	decreased fertilization frequency	Prss55<em1Osb>/Prss55<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32301961
MGI:6454994	M	MP:0001922	reduced male fertility	Prss55<em1Osb>/Prss55<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32301961
MGI:6454995	M	MP:0031012	impaired sperm migration in female genital tract	Del(14Prss51-Prss55)3Osb/Del(14Prss51-Prss55)3Osb	involves: C57BL/6J * DBA/2J	N	32301961
MGI:6454995	M	MP:0005389	reproductive system phenotype	Del(14Prss51-Prss55)3Osb/Del(14Prss51-Prss55)3Osb	involves: C57BL/6J * DBA/2J	Y	32301961
MGI:6454995	M	MP:0001925	male infertility	Del(14Prss51-Prss55)3Osb/Del(14Prss51-Prss55)3Osb	involves: C57BL/6J * DBA/2J	N	32301961
MGI:6454995	M	MP:0030978	impaired binding of sperm to zona pellucida	Del(14Prss51-Prss55)3Osb/Del(14Prss51-Prss55)3Osb	involves: C57BL/6J * DBA/2J	N	32301961
MGI:6454995	M	MP:0009647	decreased fertilization frequency	Del(14Prss51-Prss55)3Osb/Del(14Prss51-Prss55)3Osb	involves: C57BL/6J * DBA/2J	N	32301961
MGI:6455013	M	MP:0002675	asthenozoospermia	Tmprss12<em4Osb>/Tmprss12<em4Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32529245
MGI:6455013	M	MP:0000242	impaired fertilization	Tmprss12<em4Osb>/Tmprss12<em4Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32529245
MGI:6455013	M	MP:0031012	impaired sperm migration in female genital tract	Tmprss12<em4Osb>/Tmprss12<em4Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32529245
MGI:6455013	M	MP:0030978	impaired binding of sperm to zona pellucida	Tmprss12<em4Osb>/Tmprss12<em4Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32529245
MGI:6455013	M	MP:0001925	male infertility	Tmprss12<em4Osb>/Tmprss12<em4Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32529245
MGI:6455015	M	MP:0001925	male infertility	Cib4<em1Osb>/Cib4<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32430498
MGI:6455015	M	MP:0004852	decreased testis weight	Cib4<em1Osb>/Cib4<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32430498
MGI:6455015	M	MP:0006380	abnormal spermatid morphology	Cib4<em1Osb>/Cib4<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32430498
MGI:6455015	M	MP:0001156	abnormal spermatogenesis	Cib4<em1Osb>/Cib4<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32430498
MGI:6455015	M	MP:0009230	abnormal sperm head morphology	Cib4<em1Osb>/Cib4<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32430498
MGI:6455140	F	MP:0001935	decreased litter size	Exosc10<em1Dean>/Exosc10<em1Dean>	involves: C57BL/6J * DBA/2J	N	32313933
MGI:6455140	F	MP:0005431	decreased oocyte number	Exosc10<em1Dean>/Exosc10<em1Dean>	involves: C57BL/6J * DBA/2J	N	32313933
MGI:6455140	F	MP:0001923	reduced female fertility	Exosc10<em1Dean>/Exosc10<em1Dean>	involves: C57BL/6J * DBA/2J	N	32313933
MGI:6455140	F	MP:0012128	abnormal blastocyst formation	Exosc10<em1Dean>/Exosc10<em1Dean>	involves: C57BL/6J * DBA/2J	N	32313933
MGI:6455140	F	MP:0001125	abnormal oocyte morphology	Exosc10<em1Dean>/Exosc10<em1Dean>	involves: C57BL/6J * DBA/2J	N	32313933
MGI:6455163	M	MP:0014052	increased male germ cell apoptosis	Prr19<em1Atot>/Prr19<em1Atot>	either: (involves: C57BL/6JCrl) or (involves: CD-1)	N	32555348
MGI:6455163	F	MP:0001926	female infertility	Prr19<em1Atot>/Prr19<em1Atot>	either: (involves: C57BL/6JCrl) or (involves: CD-1)	N	32555348
MGI:6455163	F	MP:0005431	decreased oocyte number	Prr19<em1Atot>/Prr19<em1Atot>	either: (involves: C57BL/6JCrl) or (involves: CD-1)	N	32555348
MGI:6455163	M	MP:0005578	teratozoospermia	Prr19<em1Atot>/Prr19<em1Atot>	either: (involves: C57BL/6JCrl) or (involves: CD-1)	N	32555348
MGI:6455163	M	MP:0002687	oligozoospermia	Prr19<em1Atot>/Prr19<em1Atot>	either: (involves: C57BL/6JCrl) or (involves: CD-1)	N	32555348
MGI:6455163	M	MP:0004852	decreased testis weight	Prr19<em1Atot>/Prr19<em1Atot>	either: (involves: C57BL/6JCrl) or (involves: CD-1)	N	32555348
MGI:6455163	M	MP:0001925	male infertility	Prr19<em1Atot>/Prr19<em1Atot>	either: (involves: C57BL/6JCrl) or (involves: CD-1)	N	32555348
MGI:6455163	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Prr19<em1Atot>/Prr19<em1Atot>	either: (involves: C57BL/6JCrl) or (involves: CD-1)	N	32555348
MGI:6455427	M	MP:0005389	reproductive system phenotype	1700121C10Rik<em1Smoc>/1700121C10Rik<em1Smoc>	involves: C57BL/6J	Y	31801914
MGI:6455746	M	MP:0001156	abnormal spermatogenesis	Skp1<tm1.1Jw>/Skp1<tm1.2Jw>,Tg(Ddx4-cre/ERT2)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	32232159
MGI:6455746	F	MP:0005168	abnormal female meiosis	Skp1<tm1.1Jw>/Skp1<tm1.2Jw>,Tg(Ddx4-cre/ERT2)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	32232159
MGI:6455746	F	MP:0009093	oocyte degeneration	Skp1<tm1.1Jw>/Skp1<tm1.2Jw>,Tg(Ddx4-cre/ERT2)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	32232159
MGI:6455746	F	MP:0003718	maternal effect	Skp1<tm1.1Jw>/Skp1<tm1.2Jw>,Tg(Ddx4-cre/ERT2)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	32232159
MGI:6455746	F	MP:0001926	female infertility	Skp1<tm1.1Jw>/Skp1<tm1.2Jw>,Tg(Ddx4-cre/ERT2)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	32232159
MGI:6455746	M	MP:0008261	arrest of male meiosis	Skp1<tm1.1Jw>/Skp1<tm1.2Jw>,Tg(Ddx4-cre/ERT2)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	32232159
MGI:6455746	M	MP:0005159	azoospermia	Skp1<tm1.1Jw>/Skp1<tm1.2Jw>,Tg(Ddx4-cre/ERT2)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	32232159
MGI:6455746	M	MP:0004852	decreased testis weight	Skp1<tm1.1Jw>/Skp1<tm1.2Jw>,Tg(Ddx4-cre/ERT2)1Dcas/0	involves: 129S4/SvJae * C57BL/6 * FVB/N	N	32232159
MGI:6456828	M	MP:0009451	abnormal chromosomal synapsis	Brme1<em1Hirok>/Brme1<em1Hirok>	C57BL/6J-Brme1<em1Hirok>	N	32345962
MGI:6456828	M	MP:0008966	abnormal chiasmata formation	Brme1<em1Hirok>/Brme1<em1Hirok>	C57BL/6J-Brme1<em1Hirok>	N	32345962
MGI:6456828	M	MP:0001147	small testis	Brme1<em1Hirok>/Brme1<em1Hirok>	C57BL/6J-Brme1<em1Hirok>	N	32345962
MGI:6456828	M	MP:0014052	increased male germ cell apoptosis	Brme1<em1Hirok>/Brme1<em1Hirok>	C57BL/6J-Brme1<em1Hirok>	N	32345962
MGI:6456828	M	MP:0010948	abnormal double-strand DNA break repair	Brme1<em1Hirok>/Brme1<em1Hirok>	C57BL/6J-Brme1<em1Hirok>	N	32345962
MGI:6456828	M	MP:0001925	male infertility	Brme1<em1Hirok>/Brme1<em1Hirok>	C57BL/6J-Brme1<em1Hirok>	N	32345962
MGI:6456828	M	MP:0005169	abnormal male meiosis	Brme1<em1Hirok>/Brme1<em1Hirok>	C57BL/6J-Brme1<em1Hirok>	N	32345962
MGI:6456828	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Brme1<em1Hirok>/Brme1<em1Hirok>	C57BL/6J-Brme1<em1Hirok>	N	32345962
MGI:6456828	M	MP:0005159	azoospermia	Brme1<em1Hirok>/Brme1<em1Hirok>	C57BL/6J-Brme1<em1Hirok>	N	32345962
MGI:6456829	M	MP:0001925	male infertility	Hsf2bp<tm1b(EUCOMM)Hmgu>/Hsf2bp<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N	N	32345962
MGI:6456829	M	MP:0010948	abnormal double-strand DNA break repair	Hsf2bp<tm1b(EUCOMM)Hmgu>/Hsf2bp<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N	N	32345962
MGI:6456832	M	MP:0010948	abnormal double-strand DNA break repair	Meiob<tm1.1Jw>/Meiob<tm1.1Jw>	involves: 129S4/SvJae * C57BL/6	N	32345962
MGI:6456856	M	MP:0001925	male infertility	Gsk3a<tm1.2Svij>/Gsk3a<tm1.2Svij>	involves: 129S4/SvJaeSor * C57BL/6	N	25568307
MGI:6456856	M	MP:0009831	abnormal sperm midpiece morphology	Gsk3a<tm1.2Svij>/Gsk3a<tm1.2Svij>	involves: 129S4/SvJaeSor * C57BL/6	N	25568307
MGI:6456856	M	MP:0002675	asthenozoospermia	Gsk3a<tm1.2Svij>/Gsk3a<tm1.2Svij>	involves: 129S4/SvJaeSor * C57BL/6	N	25568307
MGI:6456856	M	MP:0009230	abnormal sperm head morphology	Gsk3a<tm1.2Svij>/Gsk3a<tm1.2Svij>	involves: 129S4/SvJaeSor * C57BL/6	N	25568307
MGI:6456856	M	MP:0002687	oligozoospermia	Gsk3a<tm1.2Svij>/Gsk3a<tm1.2Svij>	involves: 129S4/SvJaeSor * C57BL/6	N	25568307
MGI:6456857	M	MP:0009230	abnormal sperm head morphology	Gsk3a<tm1.2Svij>/Gsk3a<+>	involves: 129S4/SvJaeSor * C57BL/6	N	25568307
MGI:6456857	M	MP:0005389	reproductive system phenotype	Gsk3a<tm1.2Svij>/Gsk3a<+>	involves: 129S4/SvJaeSor * C57BL/6	Y	25568307
MGI:6456857	M	MP:0009831	abnormal sperm midpiece morphology	Gsk3a<tm1.2Svij>/Gsk3a<+>	involves: 129S4/SvJaeSor * C57BL/6	N	25568307
MGI:6456969	M	MP:0001447	abnormal nest building behavior	Gpr88<tm1.2Ics>/Gpr88<tm1.2Ics>	involves: 129 * C57BL/6J	N	26188600
MGI:6457113	F	MP:0011290	decreased nephron number	Mir210<tm1Mtm>/Mir210<tm1Mtm>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * BALB/cJ	N	32141129
MGI:6457113	M	MP:0011290	decreased nephron number	Mir210<tm1Mtm>/Mir210<tm1Mtm>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * BALB/cJ	N	32141129
MGI:6457113	F	MP:0002135	abnormal kidney morphology	Mir210<tm1Mtm>/Mir210<tm1Mtm>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * BALB/cJ	N	32141129
MGI:6457113	M	MP:0002135	abnormal kidney morphology	Mir210<tm1Mtm>/Mir210<tm1Mtm>	involves: 129P2/OlaHsd * 129S4/SvJaeSor * BALB/cJ	N	32141129
MGI:6457270	M	MP:0002216	abnormal seminiferous tubule morphology	Pramex1<tm1c(KOMP)Wtsi>/Y,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N	N	32017313
MGI:6457270	M	MP:0001155	arrest of spermatogenesis	Pramex1<tm1c(KOMP)Wtsi>/Y,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N	N	32017313
MGI:6457270	M	MP:0001156	abnormal spermatogenesis	Pramex1<tm1c(KOMP)Wtsi>/Y,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N	N	32017313
MGI:6457270	M	MP:0014052	increased male germ cell apoptosis	Pramex1<tm1c(KOMP)Wtsi>/Y,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N	N	32017313
MGI:6457270	M	MP:0013601	increased testis apoptosis	Pramex1<tm1c(KOMP)Wtsi>/Y,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N	N	32017313
MGI:6457270	M	MP:0004901	decreased male germ cell number	Pramex1<tm1c(KOMP)Wtsi>/Y,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N	N	32017313
MGI:6457270	M	MP:0006428	ectopic Sertoli cells	Pramex1<tm1c(KOMP)Wtsi>/Y,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N	N	32017313
MGI:6457270	M	MP:0006379	abnormal spermatocyte morphology	Pramex1<tm1c(KOMP)Wtsi>/Y,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N	N	32017313
MGI:6457270	M	MP:0004852	decreased testis weight	Pramex1<tm1c(KOMP)Wtsi>/Y,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N	N	32017313
MGI:6457270	M	MP:0002687	oligozoospermia	Pramex1<tm1c(KOMP)Wtsi>/Y,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N	N	32017313
MGI:6457270	M	MP:0001147	small testis	Pramex1<tm1c(KOMP)Wtsi>/Y,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N	N	32017313
MGI:6457270	M	MP:0005389	reproductive system phenotype	Pramex1<tm1c(KOMP)Wtsi>/Y,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N	Y	32017313
MGI:6457281	M	MP:0005290	decreased oxygen consumption	Opn3<tm2b(EUCOMM)Wtsi>/Opn3<tm2b(EUCOMM)Wtsi>	involves: C57BL/6N * FVB/N	N	31968245
MGI:6457281	M	MP:0004890	decreased energy expenditure	Opn3<tm2b(EUCOMM)Wtsi>/Opn3<tm2b(EUCOMM)Wtsi>	involves: C57BL/6N * FVB/N	N	31968245
MGI:6457281	M	MP:0008963	increased carbon dioxide production	Opn3<tm2b(EUCOMM)Wtsi>/Opn3<tm2b(EUCOMM)Wtsi>	involves: C57BL/6N * FVB/N	N	31968245
MGI:6457570	M	MP:0008892	abnormal sperm flagellum morphology	Cfap43<em1Sono>/Cfap43<em1Sono>	Not Specified	N	31004071
MGI:6458045	F	MP:0010025	decreased total body fat amount	Smdt1<em2Fink>/Smdt1<em2Fink>	involves: C57BL/6J * C57BL/6N * CBA/J * CD-1	N	32017711
MGI:6458057	M	MP:0001922	reduced male fertility	Csl<tm1(KOMP)Vlcg>/Csl<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	31857692
MGI:6458057	M	MP:0010958	abnormal tricarboxylic acid cycle	Csl<tm1(KOMP)Vlcg>/Csl<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	31857692
MGI:6458057	M	MP:0001935	decreased litter size	Csl<tm1(KOMP)Vlcg>/Csl<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	31857692
MGI:6458057	M	MP:0005584	abnormal enzyme/coenzyme activity	Csl<tm1(KOMP)Vlcg>/Csl<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	31857692
MGI:6458057	M	MP:0003806	abnormal nucleotide metabolism	Csl<tm1(KOMP)Vlcg>/Csl<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	31857692
MGI:6458057	M	MP:0005389	reproductive system phenotype	Csl<tm1(KOMP)Vlcg>/Csl<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	Y	31857692
MGI:6458057	M	MP:0004543	abnormal sperm physiology	Csl<tm1(KOMP)Vlcg>/Csl<tm1(KOMP)Vlcg>	involves: C57BL/6NTac	N	31857692
MGI:6458554	M	MP:0020451	decreased sperm progressive motility	Cmtm4<em1Wlh>/Cmtm4<em1Wlh>	involves: C57BL/6J	N	30867229
MGI:6458554	M	MP:0005389	reproductive system phenotype	Cmtm4<em1Wlh>/Cmtm4<em1Wlh>	involves: C57BL/6J	Y	30867229
MGI:6458554	M	MP:0009230	abnormal sperm head morphology	Cmtm4<em1Wlh>/Cmtm4<em1Wlh>	involves: C57BL/6J	N	30867229
MGI:6458554	M	MP:0001922	reduced male fertility	Cmtm4<em1Wlh>/Cmtm4<em1Wlh>	involves: C57BL/6J	N	30867229
MGI:6458554	M	MP:0002687	oligozoospermia	Cmtm4<em1Wlh>/Cmtm4<em1Wlh>	involves: C57BL/6J	N	30867229
MGI:6458554	M	MP:0009831	abnormal sperm midpiece morphology	Cmtm4<em1Wlh>/Cmtm4<em1Wlh>	involves: C57BL/6J	N	30867229
MGI:6458876	M	MP:0013618	decreased areal bone mineral density	Zbtb40<em1Clab>/Zbtb40<em1Clab>	C57BL/6J-Zbtb40<em1Clab>	N	32497039
MGI:6458876	M	MP:0010869	decreased bone trabecula number	Zbtb40<em1Clab>/Zbtb40<em1Clab>	C57BL/6J-Zbtb40<em1Clab>	N	32497039
MGI:6458876	M	MP:0010873	decreased trabecular bone mass	Zbtb40<em1Clab>/Zbtb40<em1Clab>	C57BL/6J-Zbtb40<em1Clab>	N	32497039
MGI:6458876	M	MP:0010879	decreased trabecular bone volume	Zbtb40<em1Clab>/Zbtb40<em1Clab>	C57BL/6J-Zbtb40<em1Clab>	N	32497039
MGI:6458876	M	MP:0010933	decreased trabecular bone connectivity density	Zbtb40<em1Clab>/Zbtb40<em1Clab>	C57BL/6J-Zbtb40<em1Clab>	N	32497039
MGI:6458883	F	MP:0013618	decreased areal bone mineral density	Wnt4<tm1.1Bhr>/Wnt4<tm1.1Bhr>,Tg(Prrx1-cre)1Cjt/0	involves: 129S7/SvEvBrd * C57BL/6J	N	32497039
MGI:6458883	F	MP:0021182	decreased femoral compact bone area	Wnt4<tm1.1Bhr>/Wnt4<tm1.1Bhr>,Tg(Prrx1-cre)1Cjt/0	involves: 129S7/SvEvBrd * C57BL/6J	N	32497039
MGI:6458883	F	MP:0020010	decreased bone mineral density of femur	Wnt4<tm1.1Bhr>/Wnt4<tm1.1Bhr>,Tg(Prrx1-cre)1Cjt/0	involves: 129S7/SvEvBrd * C57BL/6J	N	32497039
MGI:6458883	F	MP:0010873	decreased trabecular bone mass	Wnt4<tm1.1Bhr>/Wnt4<tm1.1Bhr>,Tg(Prrx1-cre)1Cjt/0	involves: 129S7/SvEvBrd * C57BL/6J	N	32497039
MGI:6459715	M	MP:0002216	abnormal seminiferous tubule morphology	Gmnc<tm1.1Strc>/Gmnc<tm1.1Strc>	involves: C57BL/6 * CBA	N	26933123
MGI:6459715	F	MP:0009070	small oviduct	Gmnc<tm1.1Strc>/Gmnc<tm1.1Strc>	involves: C57BL/6 * CBA	N	26933123
MGI:6459715	F	MP:0031381	decreased secondary ovarian follicle number	Gmnc<tm1.1Strc>/Gmnc<tm1.1Strc>	involves: C57BL/6 * CBA	N	26933123
MGI:6459715	F	MP:0001926	female infertility	Gmnc<tm1.1Strc>/Gmnc<tm1.1Strc>	involves: C57BL/6 * CBA	N	26933123
MGI:6459715	F	MP:0013236	ovary degeneration	Gmnc<tm1.1Strc>/Gmnc<tm1.1Strc>	involves: C57BL/6 * CBA	N	26933123
MGI:6459715	M	MP:0001925	male infertility	Gmnc<tm1.1Strc>/Gmnc<tm1.1Strc>	involves: C57BL/6 * CBA	N	26933123
MGI:6459715	F	MP:0001127	small ovary	Gmnc<tm1.1Strc>/Gmnc<tm1.1Strc>	involves: C57BL/6 * CBA	N	26933123
MGI:6459715	M	MP:0005159	azoospermia	Gmnc<tm1.1Strc>/Gmnc<tm1.1Strc>	involves: C57BL/6 * CBA	N	26933123
MGI:6459715	F	MP:0009363	abnormal tertiary ovarian follicle morphology	Gmnc<tm1.1Strc>/Gmnc<tm1.1Strc>	involves: C57BL/6 * CBA	N	26933123
MGI:6459715	M	MP:0006380	abnormal spermatid morphology	Gmnc<tm1.1Strc>/Gmnc<tm1.1Strc>	involves: C57BL/6 * CBA	N	26933123
MGI:6459715	F	MP:0011645	absent oviduct epithelium motile cilium	Gmnc<tm1.1Strc>/Gmnc<tm1.1Strc>	involves: C57BL/6 * CBA	N	26933123
MGI:6459715	F	MP:0011121	decreased primordial ovarian follicle number	Gmnc<tm1.1Strc>/Gmnc<tm1.1Strc>	involves: C57BL/6 * CBA	N	26933123
MGI:6459715	M	MP:0001156	abnormal spermatogenesis	Gmnc<tm1.1Strc>/Gmnc<tm1.1Strc>	involves: C57BL/6 * CBA	N	26933123
MGI:6459876	M	MP:0005389	reproductive system phenotype	Spmip4<em1Osb>/Spmip4<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	32588039
MGI:6459877	M	MP:0005389	reproductive system phenotype	Allc<em1Osb>/Allc<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588039
MGI:6459878	M	MP:0005389	reproductive system phenotype	Fam229b<em1Osb>/Fam229b<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588039
MGI:6459879	M	MP:0005389	reproductive system phenotype	Fscb<em1Osb>/Fscb<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588039
MGI:6459881	M	MP:0005389	reproductive system phenotype	Iqca1<em1Osb>/Iqca1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588039
MGI:6459882	M	MP:0005389	reproductive system phenotype	Lelp1<em1Osb>/Lelp1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588039
MGI:6459883	M	MP:0005389	reproductive system phenotype	Spata24<em1Osb>/Spata24<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588039
MGI:6459884	M	MP:0005389	reproductive system phenotype	Hdgfl1<em1Osb>/Hdgfl1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588039
MGI:6459885	M	MP:0005389	reproductive system phenotype	Tmem97<em1Osb>/Tmem97<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588039
MGI:6459886	M	MP:0005389	reproductive system phenotype	Lrcol1<em1Osb>/Lrcol1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588039
MGI:6459887	M	MP:0005389	reproductive system phenotype	Tmem114<em1Osb>/Tmem114<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588039
MGI:6459888	M	MP:0005389	reproductive system phenotype	Cabs1<em1Osb>/Cabs1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588039
MGI:6459889	M	MP:0005389	reproductive system phenotype	Eddm3b<em1Osb>/Eddm3b<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32588039
MGI:6459915	M	MP:0001751	increased circulating luteinizing hormone level	Dcp2<tm1Smoc>/Dcp2<tm1Smoc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	32245620
MGI:6459915	M	MP:0014052	increased male germ cell apoptosis	Dcp2<tm1Smoc>/Dcp2<tm1Smoc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	32245620
MGI:6459915	M	MP:0002675	asthenozoospermia	Dcp2<tm1Smoc>/Dcp2<tm1Smoc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	32245620
MGI:6459915	M	MP:0001750	increased circulating follicle stimulating hormone level	Dcp2<tm1Smoc>/Dcp2<tm1Smoc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	32245620
MGI:6459915	M	MP:0004852	decreased testis weight	Dcp2<tm1Smoc>/Dcp2<tm1Smoc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	32245620
MGI:6459915	M	MP:0001925	male infertility	Dcp2<tm1Smoc>/Dcp2<tm1Smoc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	32245620
MGI:6459915	M	MP:0004901	decreased male germ cell number	Dcp2<tm1Smoc>/Dcp2<tm1Smoc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	32245620
MGI:6459915	M	MP:0002780	decreased circulating testosterone level	Dcp2<tm1Smoc>/Dcp2<tm1Smoc>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	32245620
MGI:6460081	M	MP:0006428	ectopic Sertoli cells	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0020355	abnormal Sertoli cell barrier morphology	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0020378	abnormal cell cytoskeleton morphology	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0006420	abnormal peritubular myoid cell morphology	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0001154	seminiferous tubule degeneration	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0005250	decreased Sertoli cell number	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0005159	azoospermia	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0004852	decreased testis weight	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0013600	testis degeneration	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0002216	abnormal seminiferous tubule morphology	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0006380	abnormal spermatid morphology	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0004929	decreased epididymis weight	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0001932	abnormal spermiogenesis	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0013601	increased testis apoptosis	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0020362	abnormal male germ cell physiology	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0001925	male infertility	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0004901	decreased male germ cell number	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460081	M	MP:0003830	abnormal testis development	Rptor<tm1.1Dmsa>/Rptor<tm1.1Dmsa>,Tg(Amh-cre)8815Reb/0	involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N	N	29961810
MGI:6460092	M	MP:0002687	oligozoospermia	Rheb<tm1Pfw>/Rheb<tm1Pfw>,Tg(Amh-cre)8815Reb/0	involves: 129S1/SvImJ * FVB/N	N	29961810
MGI:6460092	M	MP:0005389	reproductive system phenotype	Rheb<tm1Pfw>/Rheb<tm1Pfw>,Tg(Amh-cre)8815Reb/0	involves: 129S1/SvImJ * FVB/N	Y	29961810
MGI:6460092	M	MP:0004929	decreased epididymis weight	Rheb<tm1Pfw>/Rheb<tm1Pfw>,Tg(Amh-cre)8815Reb/0	involves: 129S1/SvImJ * FVB/N	N	29961810
MGI:6460092	M	MP:0004852	decreased testis weight	Rheb<tm1Pfw>/Rheb<tm1Pfw>,Tg(Amh-cre)8815Reb/0	involves: 129S1/SvImJ * FVB/N	N	29961810
MGI:6460092	M	MP:0002216	abnormal seminiferous tubule morphology	Rheb<tm1Pfw>/Rheb<tm1Pfw>,Tg(Amh-cre)8815Reb/0	involves: 129S1/SvImJ * FVB/N	N	29961810
MGI:6460114	M	MP:0002216	abnormal seminiferous tubule morphology	Scaper<tm1a(EUCOMM)Hmgu>/Scaper<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	32510560
MGI:6460114	M	MP:0001153	small seminiferous tubules	Scaper<tm1a(EUCOMM)Hmgu>/Scaper<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	32510560
MGI:6460114	M	MP:0001925	male infertility	Scaper<tm1a(EUCOMM)Hmgu>/Scaper<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	32510560
MGI:6460114	F	MP:0011129	decreased tertiary ovarian follicle number	Scaper<tm1a(EUCOMM)Hmgu>/Scaper<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	32510560
MGI:6460114	M	MP:0005159	azoospermia	Scaper<tm1a(EUCOMM)Hmgu>/Scaper<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	32510560
MGI:6460114	M	MP:0001147	small testis	Scaper<tm1a(EUCOMM)Hmgu>/Scaper<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	32510560
MGI:6460114	F	MP:0001935	decreased litter size	Scaper<tm1a(EUCOMM)Hmgu>/Scaper<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	32510560
MGI:6460114	F	MP:0011121	decreased primordial ovarian follicle number	Scaper<tm1a(EUCOMM)Hmgu>/Scaper<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	32510560
MGI:6460114	F	MP:0031239	increased atretic ovarian follicle number	Scaper<tm1a(EUCOMM)Hmgu>/Scaper<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	32510560
MGI:6460114	F	MP:0001923	reduced female fertility	Scaper<tm1a(EUCOMM)Hmgu>/Scaper<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	32510560
MGI:6460114	M	MP:0004852	decreased testis weight	Scaper<tm1a(EUCOMM)Hmgu>/Scaper<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	32510560
MGI:6460293	M	MP:0001925	male infertility	Brme1<em1Zhal>/Brme1<em1Zhal>	involves: C57BL/6	N	32463460
MGI:6460293	M	MP:0005159	azoospermia	Brme1<em1Zhal>/Brme1<em1Zhal>	involves: C57BL/6	N	32463460
MGI:6460293	F	MP:0005389	reproductive system phenotype	Brme1<em1Zhal>/Brme1<em1Zhal>	involves: C57BL/6	Y	32463460
MGI:6460293	M	MP:0014052	increased male germ cell apoptosis	Brme1<em1Zhal>/Brme1<em1Zhal>	involves: C57BL/6	N	32463460
MGI:6460293	M	MP:0006379	abnormal spermatocyte morphology	Brme1<em1Zhal>/Brme1<em1Zhal>	involves: C57BL/6	N	32463460
MGI:6460293	M	MP:0006380	abnormal spermatid morphology	Brme1<em1Zhal>/Brme1<em1Zhal>	involves: C57BL/6	N	32463460
MGI:6460293	M	MP:0005169	abnormal male meiosis	Brme1<em1Zhal>/Brme1<em1Zhal>	involves: C57BL/6	N	32463460
MGI:6460293	M	MP:0002216	abnormal seminiferous tubule morphology	Brme1<em1Zhal>/Brme1<em1Zhal>	involves: C57BL/6	N	32463460
MGI:6460293	M	MP:0001147	small testis	Brme1<em1Zhal>/Brme1<em1Zhal>	involves: C57BL/6	N	32463460
MGI:6460293	M	MP:0010948	abnormal double-strand DNA break repair	Brme1<em1Zhal>/Brme1<em1Zhal>	involves: C57BL/6	N	32463460
MGI:6460304	M	MP:0001925	male infertility	Nell2<em1Osb>/Nell2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32499443
MGI:6460304	M	MP:0002660	abnormal caput epididymis morphology	Nell2<em1Osb>/Nell2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32499443
MGI:6460305	M	MP:0031012	impaired sperm migration in female genital tract	Nell2<em1Osb>/Nell2<em1Osb>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: C57BL/6NJcl * DBA/2NJcl	N	32499443
MGI:6460305	M	MP:0030978	impaired binding of sperm to zona pellucida	Nell2<em1Osb>/Nell2<em1Osb>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: C57BL/6NJcl * DBA/2NJcl	N	32499443
MGI:6460306	M	MP:0005389	reproductive system phenotype	Nell2<em1Osb>/Nell2<em1Osb>,Tg(Clgn-Nell2)#Osb/0	involves: C57BL/6NJcl * DBA/2NJcl	Y	32499443
MGI:6460307	M	MP:0031012	impaired sperm migration in female genital tract	Ovch2<em1Osb>/Ovch2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32499443
MGI:6460307	M	MP:0001925	male infertility	Ovch2<em1Osb>/Ovch2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32499443
MGI:6460307	M	MP:0030978	impaired binding of sperm to zona pellucida	Ovch2<em1Osb>/Ovch2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32499443
MGI:6460308	M	MP:0005389	reproductive system phenotype	Adam28<em1Osb>/Adam28<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	32499443
MGI:6460309	M	MP:0001925	male infertility	Ros1<em1Osb>/Ros1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32499443
MGI:6460309	M	MP:0030978	impaired binding of sperm to zona pellucida	Ros1<em1Osb>/Ros1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32499443
MGI:6460370	M	MP:0008279	arrest of spermiogenesis	Zfp628<em1Frei>/Zfp628<em1Frei>	involves: CD-1	N	31932482
MGI:6460370	M	MP:0001147	small testis	Zfp628<em1Frei>/Zfp628<em1Frei>	involves: CD-1	N	31932482
MGI:6460370	F	MP:0005389	reproductive system phenotype	Zfp628<em1Frei>/Zfp628<em1Frei>	involves: CD-1	Y	31932482
MGI:6460370	M	MP:0008898	abnormal acrosome morphology	Zfp628<em1Frei>/Zfp628<em1Frei>	involves: CD-1	N	31932482
MGI:6460370	M	MP:0001925	male infertility	Zfp628<em1Frei>/Zfp628<em1Frei>	involves: CD-1	N	31932482
MGI:6460370	M	MP:0020550	multinucleated giant male germ cells	Zfp628<em1Frei>/Zfp628<em1Frei>	involves: CD-1	N	31932482
MGI:6460370	M	MP:0005159	azoospermia	Zfp628<em1Frei>/Zfp628<em1Frei>	involves: CD-1	N	31932482
MGI:6460370	M	MP:0014052	increased male germ cell apoptosis	Zfp628<em1Frei>/Zfp628<em1Frei>	involves: CD-1	N	31932482
MGI:6460372	M	MP:0001147	small testis	Zfp628<em1Frei>/Zfp628<+>	involves: CD-1	N	31932482
MGI:6460372	M	MP:0004901	decreased male germ cell number	Zfp628<em1Frei>/Zfp628<+>	involves: CD-1	N	31932482
MGI:6460451	M	MP:0001925	male infertility	Tmem95<em1Beal>/Tmem95<em1Beal>	involves: C57BL/6 * CBA	N	32484434
MGI:6460451	M	MP:0000242	impaired fertilization	Tmem95<em1Beal>/Tmem95<em1Beal>	involves: C57BL/6 * CBA	N	32484434
MGI:6460451	M	MP:0031010	failure of sperm-egg fusion	Tmem95<em1Beal>/Tmem95<em1Beal>	involves: C57BL/6 * CBA	N	32484434
MGI:6460468	M	MP:0000242	impaired fertilization	4930451I11Rik<em1Osb>/4930451I11Rik<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32295885
MGI:6460468	M	MP:0001922	reduced male fertility	4930451I11Rik<em1Osb>/4930451I11Rik<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32295885
MGI:6460468	M	MP:0005389	reproductive system phenotype	4930451I11Rik<em1Osb>/4930451I11Rik<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	32295885
MGI:6460469	M	MP:0000242	impaired fertilization	4930451I11Rik<em2Osb>/4930451I11Rik<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32295885
MGI:6461014	M	MP:0005562	decreased mean corpuscular hemoglobin	1700019D03Rik<tm1.1(NCOM)Mfgc>/1700019D03Rik<tm1.1(NCOM)Mfgc>	C57BL/6N-1700019D03Rik<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:6461014	M	MP:0000702	enlarged lymph nodes	1700019D03Rik<tm1.1(NCOM)Mfgc>/1700019D03Rik<tm1.1(NCOM)Mfgc>	C57BL/6N-1700019D03Rik<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:6461014	M	MP:0005505	thrombocytosis	1700019D03Rik<tm1.1(NCOM)Mfgc>/1700019D03Rik<tm1.1(NCOM)Mfgc>	C57BL/6N-1700019D03Rik<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:6461015	F	MP:0005344	increased circulating bilirubin level	1700025G04Rik<em1(IMPC)Mbp>/1700025G04Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700025G04Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461015	M	MP:0010067	increased red blood cell distribution width	1700025G04Rik<em1(IMPC)Mbp>/1700025G04Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700025G04Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461015	M	MP:0001293	anophthalmia	1700025G04Rik<em1(IMPC)Mbp>/1700025G04Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700025G04Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461015	M	MP:0002590	increased mean corpuscular volume	1700025G04Rik<em1(IMPC)Mbp>/1700025G04Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700025G04Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461015	M	MP:0002092	abnormal eye morphology	1700025G04Rik<em1(IMPC)Mbp>/1700025G04Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700025G04Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461015	M	MP:0001529	abnormal vocalization	1700025G04Rik<em1(IMPC)Mbp>/1700025G04Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700025G04Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	F	MP:0002135	abnormal kidney morphology	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	F	MP:0001126	abnormal ovary morphology	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	F	MP:0002968	increased circulating alkaline phosphatase level	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	M	MP:0002997	enlarged seminal vesicle	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	M	MP:0000470	abnormal stomach morphology	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	F	MP:0000689	abnormal spleen morphology	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	M	MP:0002092	abnormal eye morphology	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	M	MP:0001293	anophthalmia	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	F	MP:0000691	enlarged spleen	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	M	MP:0002060	abnormal skin morphology	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	M	MP:0000598	abnormal liver morphology	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	M	MP:0000702	enlarged lymph nodes	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	M	MP:0002339	abnormal lymph node morphology	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461017	M	MP:0000599	enlarged liver	1700034E13Rik<em1(IMPC)Mbp>/1700034E13Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700034E13Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461018	F	MP:0000709	enlarged thymus	1700069L16Rik<em1(IMPC)Mbp>/1700069L16Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700069L16Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461018	F	MP:0000703	abnormal thymus morphology	1700069L16Rik<em1(IMPC)Mbp>/1700069L16Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700069L16Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461018	M	MP:0000598	abnormal liver morphology	1700069L16Rik<em1(IMPC)Mbp>/1700069L16Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700069L16Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461019	F	MP:0001325	abnormal retina morphology	1700088E04Rik<tm1.1(KOMP)Vlcg>/1700088E04Rik<tm1.1(KOMP)Vlcg>	B6N(Cg)-1700088E04Rik<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461020	F	MP:0001399	hyperactivity	1700093K21Rik<em1(IMPC)J>/1700093K21Rik<em1(IMPC)J>	C57BL/6NJ-1700093K21Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461020	F	MP:0001566	increased circulating phosphate level	1700093K21Rik<em1(IMPC)J>/1700093K21Rik<em1(IMPC)J>	C57BL/6NJ-1700093K21Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461021	F	MP:0008810	increased circulating iron level	1700123O20Rik<tm1a(EUCOMM)Wtsi>/1700123O20Rik<tm1a(EUCOMM)Wtsi>	C57BL/6N-A<tm1Brd> 1700123O20Rik<tm1a(EUCOMM)Wtsi>/WtsiFlmg	N	MGI:5576271
MGI:6461022	F	MP:0001417	decreased exploration in new environment	Bltp2<em1(IMPC)J>/Bltp2<+>	C57BL/6NJ-Bltp2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461022	F	MP:0001284	absent vibrissae	Bltp2<em1(IMPC)J>/Bltp2<+>	C57BL/6NJ-Bltp2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461022	M	MP:0001312	abnormal cornea morphology	Bltp2<em1(IMPC)J>/Bltp2<+>	C57BL/6NJ-Bltp2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461023	F	MP:0002135	abnormal kidney morphology	6430548M08Rik<em1(IMPC)Mbp>/6430548M08Rik<em1(IMPC)Mbp>	C57BL/6N-6430548M08Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461023	F	MP:0002968	increased circulating alkaline phosphatase level	6430548M08Rik<em1(IMPC)Mbp>/6430548M08Rik<em1(IMPC)Mbp>	C57BL/6N-6430548M08Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461023	F	MP:0003068	enlarged kidney	6430548M08Rik<em1(IMPC)Mbp>/6430548M08Rik<em1(IMPC)Mbp>	C57BL/6N-6430548M08Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461024	F	MP:0002833	increased heart weight	A1cf<tm1b(EUCOMM)Hmgu>/A1cf<tm1b(EUCOMM)Hmgu>	B6N(Cg)-A1cf<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461024	M	MP:0010052	increased grip strength	A1cf<tm1b(EUCOMM)Hmgu>/A1cf<tm1b(EUCOMM)Hmgu>	B6N(Cg)-A1cf<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461024	M	MP:0005633	increased circulating sodium level	A1cf<tm1b(EUCOMM)Hmgu>/A1cf<tm1b(EUCOMM)Hmgu>	B6N(Cg)-A1cf<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461025	M	MP:0011110	preweaning lethality, incomplete penetrance	A2ml1<em1(IMPC)Tcp>/A2ml1<em1(IMPC)Tcp>	C57BL/6N-A2ml1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461025	M	MP:0000689	abnormal spleen morphology	A2ml1<em1(IMPC)Tcp>/A2ml1<em1(IMPC)Tcp>	C57BL/6N-A2ml1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461028	F	MP:0011965	decreased total retina thickness	Prr35<tm1b(KOMP)Wtsi>/Prr35<tm1b(KOMP)Wtsi>	C57BL/6N-Prr35<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6461028	F	MP:0003733	abnormal retina inner nuclear layer morphology	Prr35<tm1b(KOMP)Wtsi>/Prr35<tm1b(KOMP)Wtsi>	C57BL/6N-Prr35<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6461029	F	MP:0001120	abnormal uterus morphology	Aadac<em1(IMPC)Mbp>/Aadac<em1(IMPC)Mbp>	C57BL/6NCrl-Aadac<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461029	M	MP:0000706	small thymus	Aadac<em1(IMPC)Mbp>/Aadac<em1(IMPC)Mbp>	C57BL/6NCrl-Aadac<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461029	F	MP:0009709	hydrometra	Aadac<em1(IMPC)Mbp>/Aadac<em1(IMPC)Mbp>	C57BL/6NCrl-Aadac<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461029	M	MP:0002092	abnormal eye morphology	Aadac<em1(IMPC)Mbp>/Aadac<em1(IMPC)Mbp>	C57BL/6NCrl-Aadac<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461029	M	MP:0000538	abnormal urinary bladder morphology	Aadac<em1(IMPC)Mbp>/Aadac<em1(IMPC)Mbp>	C57BL/6NCrl-Aadac<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461029	M	MP:0000703	abnormal thymus morphology	Aadac<em1(IMPC)Mbp>/Aadac<em1(IMPC)Mbp>	C57BL/6NCrl-Aadac<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461029	M	MP:0000689	abnormal spleen morphology	Aadac<em1(IMPC)Mbp>/Aadac<em1(IMPC)Mbp>	C57BL/6NCrl-Aadac<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461029	M	MP:0003068	enlarged kidney	Aadac<em1(IMPC)Mbp>/Aadac<em1(IMPC)Mbp>	C57BL/6NCrl-Aadac<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461029	M	MP:0002135	abnormal kidney morphology	Aadac<em1(IMPC)Mbp>/Aadac<em1(IMPC)Mbp>	C57BL/6NCrl-Aadac<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461032	M	MP:0003960	increased lean body mass	Abcc8<em1(IMPC)J>/Abcc8<em1(IMPC)J>	C57BL/6NJ-Abcc8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461033	M	MP:0013279	increased fasting circulating glucose level	Abhd12b<em1(IMPC)J>/Abhd12b<em1(IMPC)J>	C57BL/6NJ-Abhd12b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461034	M	MP:0000702	enlarged lymph nodes	Abhd17c<em1(IMPC)Mbp>/Abhd17c<em1(IMPC)Mbp>	C57BL/6N-Abhd17c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461034	F	MP:0002989	small kidney	Abhd17c<em1(IMPC)Mbp>/Abhd17c<em1(IMPC)Mbp>	C57BL/6N-Abhd17c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461034	F	MP:0000274	enlarged heart	Abhd17c<em1(IMPC)Mbp>/Abhd17c<em1(IMPC)Mbp>	C57BL/6N-Abhd17c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461034	M	MP:0009552	urinary bladder obstruction	Abhd17c<em1(IMPC)Mbp>/Abhd17c<em1(IMPC)Mbp>	C57BL/6N-Abhd17c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461034	F	MP:0002188	small heart	Abhd17c<em1(IMPC)Mbp>/Abhd17c<em1(IMPC)Mbp>	C57BL/6N-Abhd17c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461034	M	MP:0002339	abnormal lymph node morphology	Abhd17c<em1(IMPC)Mbp>/Abhd17c<em1(IMPC)Mbp>	C57BL/6N-Abhd17c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461034	M	MP:0000598	abnormal liver morphology	Abhd17c<em1(IMPC)Mbp>/Abhd17c<em1(IMPC)Mbp>	C57BL/6N-Abhd17c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461034	F	MP:0000266	abnormal heart morphology	Abhd17c<em1(IMPC)Mbp>/Abhd17c<em1(IMPC)Mbp>	C57BL/6N-Abhd17c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461034	M	MP:0002060	abnormal skin morphology	Abhd17c<em1(IMPC)Mbp>/Abhd17c<em1(IMPC)Mbp>	C57BL/6N-Abhd17c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461034	F	MP:0002135	abnormal kidney morphology	Abhd17c<em1(IMPC)Mbp>/Abhd17c<em1(IMPC)Mbp>	C57BL/6N-Abhd17c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461034	M	MP:0002942	decreased circulating alanine transaminase level	Abhd17c<em1(IMPC)Mbp>/Abhd17c<em1(IMPC)Mbp>	C57BL/6N-Abhd17c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461034	F	MP:0002092	abnormal eye morphology	Abhd17c<em1(IMPC)Mbp>/Abhd17c<em1(IMPC)Mbp>	C57BL/6N-Abhd17c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461034	F	MP:0001297	microphthalmia	Abhd17c<em1(IMPC)Mbp>/Abhd17c<em1(IMPC)Mbp>	C57BL/6N-Abhd17c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461035	F	MP:0010053	decreased grip strength	Ablim2<em1(IMPC)J>/Ablim2<em1(IMPC)J>	C57BL/6NJ-Ablim2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461036	M	MP:0001325	abnormal retina morphology	Aco1<em1(IMPC)J>/Aco1<em1(IMPC)J>	C57BL/6NJ-Aco1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461036	M	MP:0002591	decreased mean corpuscular volume	Aco1<em1(IMPC)J>/Aco1<em1(IMPC)J>	C57BL/6NJ-Aco1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461038	M	MP:0020422	decreased freezing behavior	Acot3<em1(IMPC)Mbp>/Acot3<em1(IMPC)Mbp>	C57BL/6N-Acot3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461038	M	MP:0003068	enlarged kidney	Acot3<em1(IMPC)Mbp>/Acot3<em1(IMPC)Mbp>	C57BL/6N-Acot3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461038	F	MP:0002092	abnormal eye morphology	Acot3<em1(IMPC)Mbp>/Acot3<em1(IMPC)Mbp>	C57BL/6N-Acot3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461038	F	MP:0001297	microphthalmia	Acot3<em1(IMPC)Mbp>/Acot3<em1(IMPC)Mbp>	C57BL/6N-Acot3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461038	M	MP:0001417	decreased exploration in new environment	Acot3<em1(IMPC)Mbp>/Acot3<em1(IMPC)Mbp>	C57BL/6N-Acot3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461038	M	MP:0002135	abnormal kidney morphology	Acot3<em1(IMPC)Mbp>/Acot3<em1(IMPC)Mbp>	C57BL/6N-Acot3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461039	M	MP:0002997	enlarged seminal vesicle	Acoxl<em1(IMPC)Mbp>/Acoxl<em1(IMPC)Mbp>	C57BL/6NCrl-Acoxl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461039	M	MP:0000599	enlarged liver	Acoxl<em1(IMPC)Mbp>/Acoxl<em1(IMPC)Mbp>	C57BL/6NCrl-Acoxl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461039	M	MP:0005016	decreased lymphocyte cell number	Acoxl<em1(IMPC)Mbp>/Acoxl<em1(IMPC)Mbp>	C57BL/6NCrl-Acoxl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461039	F	MP:0002188	small heart	Acoxl<em1(IMPC)Mbp>/Acoxl<em1(IMPC)Mbp>	C57BL/6NCrl-Acoxl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461039	F	MP:0002060	abnormal skin morphology	Acoxl<em1(IMPC)Mbp>/Acoxl<em1(IMPC)Mbp>	C57BL/6NCrl-Acoxl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461039	M	MP:0002339	abnormal lymph node morphology	Acoxl<em1(IMPC)Mbp>/Acoxl<em1(IMPC)Mbp>	C57BL/6NCrl-Acoxl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461039	M	MP:0001417	decreased exploration in new environment	Acoxl<em1(IMPC)Mbp>/Acoxl<em1(IMPC)Mbp>	C57BL/6NCrl-Acoxl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461039	M	MP:0000702	enlarged lymph nodes	Acoxl<em1(IMPC)Mbp>/Acoxl<em1(IMPC)Mbp>	C57BL/6NCrl-Acoxl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461039	M	MP:0000219	increased neutrophil cell number	Acoxl<em1(IMPC)Mbp>/Acoxl<em1(IMPC)Mbp>	C57BL/6NCrl-Acoxl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461039	F	MP:0000639	abnormal adrenal gland morphology	Acoxl<em1(IMPC)Mbp>/Acoxl<em1(IMPC)Mbp>	C57BL/6NCrl-Acoxl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461039	M	MP:0000598	abnormal liver morphology	Acoxl<em1(IMPC)Mbp>/Acoxl<em1(IMPC)Mbp>	C57BL/6NCrl-Acoxl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461039	F	MP:0005292	improved glucose tolerance	Acoxl<em1(IMPC)Mbp>/Acoxl<em1(IMPC)Mbp>	C57BL/6NCrl-Acoxl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461039	M	MP:0003642	absent seminal vesicle	Acoxl<em1(IMPC)Mbp>/Acoxl<em1(IMPC)Mbp>	C57BL/6NCrl-Acoxl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461041	M	MP:0002833	increased heart weight	Acvr1c<tm1b(EUCOMM)Hmgu>/Acvr1c<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Acvr1c<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461041	M	MP:0010025	decreased total body fat amount	Acvr1c<tm1b(EUCOMM)Hmgu>/Acvr1c<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Acvr1c<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461041	M	MP:0001402	decreased locomotor activity	Acvr1c<tm1b(EUCOMM)Hmgu>/Acvr1c<tm1b(EUCOMM)Hmgu>	B6N(Cg)-Acvr1c<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461042	F	MP:0000195	decreased circulating calcium level	Acy3<em1(IMPC)J>/Acy3<em1(IMPC)J>	C57BL/6NJ-Acy3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461042	F	MP:0005567	decreased circulating total protein level	Acy3<em1(IMPC)J>/Acy3<em1(IMPC)J>	C57BL/6NJ-Acy3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461042	M	MP:0005553	increased circulating creatinine level	Acy3<em1(IMPC)J>/Acy3<em1(IMPC)J>	C57BL/6NJ-Acy3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461042	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Acy3<em1(IMPC)J>/Acy3<em1(IMPC)J>	C57BL/6NJ-Acy3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461046	M	MP:0000220	increased monocyte cell number	Agbl4<em1(IMPC)Mbp>/Agbl4<em1(IMPC)Mbp>	C57BL/6NCrl-Agbl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461046	M	MP:0005344	increased circulating bilirubin level	Agbl4<em1(IMPC)Mbp>/Agbl4<em1(IMPC)Mbp>	C57BL/6NCrl-Agbl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461049	F	MP:0005278	abnormal cholesterol homeostasis	Aire<tm1.1(NCOM)Mfgc>/Aire<+>	C57BL/6N-Aire<tm1.1(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:6461050	F	MP:0005016	decreased lymphocyte cell number	Ajuba<em1(IMPC)H>/Ajuba<em1(IMPC)H>	C57BL/6N-Ajuba<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461050	F	MP:0000219	increased neutrophil cell number	Ajuba<em1(IMPC)H>/Ajuba<em1(IMPC)H>	C57BL/6N-Ajuba<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461050	M	MP:0000572	abnormal autopod morphology	Ajuba<em1(IMPC)H>/Ajuba<em1(IMPC)H>	C57BL/6N-Ajuba<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461050	M	MP:0002110	abnormal digit morphology	Ajuba<em1(IMPC)H>/Ajuba<em1(IMPC)H>	C57BL/6N-Ajuba<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461051	F	MP:0020870	decreased thigmotaxis	Akr1c19<em1(IMPC)J>/Akr1c19<em1(IMPC)J>	C57BL/6NJ-Akr1c19<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461051	F	MP:0003131	increased erythrocyte cell number	Akr1c19<em1(IMPC)J>/Akr1c19<em1(IMPC)J>	C57BL/6NJ-Akr1c19<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461054	F	MP:0010053	decreased grip strength	Alg11<tm1.1(KOMP)Vlcg>/Alg11<+>	B6N(Cg)-Alg11<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461054	F	MP:0001289	persistence of hyaloid vascular system	Alg11<tm1.1(KOMP)Vlcg>/Alg11<+>	B6N(Cg)-Alg11<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461055	M	MP:0011962	increased cornea thickness	Alg14<tm2b(EUCOMM)Hmgu>/Alg14<+>	C57BL/6N-Alg14<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6461057	F	MP:0000689	abnormal spleen morphology	Aloxe3<em1(IMPC)Mbp>/Aloxe3<+>	C57BL/6N-Aloxe3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461057	M	MP:0002339	abnormal lymph node morphology	Aloxe3<em1(IMPC)Mbp>/Aloxe3<+>	C57BL/6N-Aloxe3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461057	F	MP:0000692	small spleen	Aloxe3<em1(IMPC)Mbp>/Aloxe3<+>	C57BL/6N-Aloxe3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461057	M	MP:0000702	enlarged lymph nodes	Aloxe3<em1(IMPC)Mbp>/Aloxe3<+>	C57BL/6N-Aloxe3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461059	F	MP:0001297	microphthalmia	Ambn<em1(IMPC)Mbp>/Ambn<em1(IMPC)Mbp>	C57BL/6N-Ambn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461059	F	MP:0002092	abnormal eye morphology	Ambn<em1(IMPC)Mbp>/Ambn<em1(IMPC)Mbp>	C57BL/6N-Ambn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461059	M	MP:0002060	abnormal skin morphology	Ambn<em1(IMPC)Mbp>/Ambn<em1(IMPC)Mbp>	C57BL/6N-Ambn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461059	F	MP:0002989	small kidney	Ambn<em1(IMPC)Mbp>/Ambn<em1(IMPC)Mbp>	C57BL/6N-Ambn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461059	M	MP:0003068	enlarged kidney	Ambn<em1(IMPC)Mbp>/Ambn<em1(IMPC)Mbp>	C57BL/6N-Ambn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461060	F	MP:0011960	abnormal eye anterior chamber depth	Ambra1<em1(IMPC)Bay>/Ambra1<+>	C57BL/6N-Ambra1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461060	F	MP:0011964	increased total retina thickness	Ambra1<em1(IMPC)Bay>/Ambra1<+>	C57BL/6N-Ambra1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461060	M	MP:0009142	decreased prepulse inhibition	Ambra1<em1(IMPC)Bay>/Ambra1<+>	C57BL/6N-Ambra1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461061	F	MP:0002339	abnormal lymph node morphology	Angpt2<em1(IMPC)Mbp>/Angpt2<+>	C57BL/6NCrl-Angpt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461061	F	MP:0000702	enlarged lymph nodes	Angpt2<em1(IMPC)Mbp>/Angpt2<+>	C57BL/6NCrl-Angpt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461063	M	MP:0001399	hyperactivity	Ankrd45<em1(IMPC)J>/Ankrd45<em1(IMPC)J>	C57BL/6NJ-Ankrd45<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461066	F	MP:0002574	increased vertical activity	Ap1s2<em1(IMPC)Mbp>/Ap1s2<em1(IMPC)Mbp>	C57BL/6N-Ap1s2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461066	F	MP:0013278	decreased fasting circulating glucose level	Ap1s2<em1(IMPC)Mbp>/Ap1s2<em1(IMPC)Mbp>	C57BL/6N-Ap1s2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461066	F	MP:0001297	microphthalmia	Ap1s2<em1(IMPC)Mbp>/Ap1s2<em1(IMPC)Mbp>	C57BL/6N-Ap1s2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461066	F	MP:0001325	abnormal retina morphology	Ap1s2<em1(IMPC)Mbp>/Ap1s2<em1(IMPC)Mbp>	C57BL/6N-Ap1s2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461066	F	MP:0002092	abnormal eye morphology	Ap1s2<em1(IMPC)Mbp>/Ap1s2<em1(IMPC)Mbp>	C57BL/6N-Ap1s2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461067	F	MP:0002075	abnormal coat/hair pigmentation	Ap2a1<em1(IMPC)J>/Ap2a1<+>	C57BL/6NJ-Ap2a1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461068	M	MP:0002075	abnormal coat/hair pigmentation	Ap2a1<em1(IMPC)J>/Ap2a1<em1(IMPC)J>	C57BL/6NJ-Ap2a1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461068	M	MP:0005562	decreased mean corpuscular hemoglobin	Ap2a1<em1(IMPC)J>/Ap2a1<em1(IMPC)J>	C57BL/6NJ-Ap2a1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461068	M	MP:0002591	decreased mean corpuscular volume	Ap2a1<em1(IMPC)J>/Ap2a1<em1(IMPC)J>	C57BL/6NJ-Ap2a1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461068	M	MP:0005554	decreased circulating creatinine level	Ap2a1<em1(IMPC)J>/Ap2a1<em1(IMPC)J>	C57BL/6NJ-Ap2a1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461068	M	MP:0001529	abnormal vocalization	Ap2a1<em1(IMPC)J>/Ap2a1<em1(IMPC)J>	C57BL/6NJ-Ap2a1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461068	M	MP:0005292	improved glucose tolerance	Ap2a1<em1(IMPC)J>/Ap2a1<em1(IMPC)J>	C57BL/6NJ-Ap2a1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461068	M	MP:0001399	hyperactivity	Ap2a1<em1(IMPC)J>/Ap2a1<em1(IMPC)J>	C57BL/6NJ-Ap2a1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461069	F	MP:0010053	decreased grip strength	Ap2b1<em1(IMPC)J>/Ap2b1<+>	C57BL/6NJ-Ap2b1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461070	M	MP:0000432	abnormal head morphology	Appbp2<em1(IMPC)J>/Appbp2<+>	C57BL/6NJ-Appbp2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461070	M	MP:0000443	abnormal snout morphology	Appbp2<em1(IMPC)J>/Appbp2<+>	C57BL/6NJ-Appbp2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461071	M	MP:0005576	decreased pulmonary ventilation	Arap1<tm1b(EUCOMM)Wtsi>/Arap1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arap1<tm1b(EUCOMM)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6461071	M	MP:0005574	decreased pulmonary respiratory rate	Arap1<tm1b(EUCOMM)Wtsi>/Arap1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arap1<tm1b(EUCOMM)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6461072	F	MP:0001399	hyperactivity	Arel1<tm1b(EUCOMM)Hmgu>/Arel1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Arel1<tm1b(EUCOMM)Hmgu>/Mhzh	N	MGI:5576271
MGI:6461072	F	MP:0013279	increased fasting circulating glucose level	Arel1<tm1b(EUCOMM)Hmgu>/Arel1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Arel1<tm1b(EUCOMM)Hmgu>/Mhzh	N	MGI:5576271
MGI:6461073	M	MP:0001146	abnormal testis morphology	Arfip1<em1(IMPC)Mbp>/Arfip1<em1(IMPC)Mbp>	C57BL/6N-Arfip1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461073	M	MP:0010123	increased bone mineral content	Arfip1<em1(IMPC)Mbp>/Arfip1<em1(IMPC)Mbp>	C57BL/6N-Arfip1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461073	F	MP:0000702	enlarged lymph nodes	Arfip1<em1(IMPC)Mbp>/Arfip1<em1(IMPC)Mbp>	C57BL/6N-Arfip1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461073	M	MP:0001147	small testis	Arfip1<em1(IMPC)Mbp>/Arfip1<em1(IMPC)Mbp>	C57BL/6N-Arfip1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461073	F	MP:0002339	abnormal lymph node morphology	Arfip1<em1(IMPC)Mbp>/Arfip1<em1(IMPC)Mbp>	C57BL/6N-Arfip1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461075	F	MP:0001258	decreased body length	Arhgap10<em1(IMPC)Tcp>/Arhgap10<em1(IMPC)Tcp>	C57BL/6N-Arhgap10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461075	F	MP:0001126	abnormal ovary morphology	Arhgap10<em1(IMPC)Tcp>/Arhgap10<em1(IMPC)Tcp>	C57BL/6N-Arhgap10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461075	F	MP:0003795	abnormal bone structure	Arhgap10<em1(IMPC)Tcp>/Arhgap10<em1(IMPC)Tcp>	C57BL/6N-Arhgap10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461075	M	MP:0002060	abnormal skin morphology	Arhgap10<em1(IMPC)Tcp>/Arhgap10<em1(IMPC)Tcp>	C57BL/6N-Arhgap10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461075	F	MP:0000702	enlarged lymph nodes	Arhgap10<em1(IMPC)Tcp>/Arhgap10<em1(IMPC)Tcp>	C57BL/6N-Arhgap10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461075	F	MP:0000157	abnormal sternum morphology	Arhgap10<em1(IMPC)Tcp>/Arhgap10<em1(IMPC)Tcp>	C57BL/6N-Arhgap10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461077	F	MP:0010124	decreased bone mineral content	Arhgap21<em1(IMPC)J>/Arhgap21<+>	C57BL/6NJ-Arhgap21<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461078	F	MP:0001566	increased circulating phosphate level	Arhgap26<tm1b(EUCOMM)Hmgu>/Arhgap26<tm1b(EUCOMM)Hmgu>	C57BL/6N-Arhgap26<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6461078	F	MP:0002591	decreased mean corpuscular volume	Arhgap26<tm1b(EUCOMM)Hmgu>/Arhgap26<tm1b(EUCOMM)Hmgu>	C57BL/6N-Arhgap26<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6461078	M	MP:0000218	increased leukocyte cell number	Arhgap26<tm1b(EUCOMM)Hmgu>/Arhgap26<tm1b(EUCOMM)Hmgu>	C57BL/6N-Arhgap26<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6461079	M	MP:0009142	decreased prepulse inhibition	Arhgap31<em1(IMPC)Bay>/Arhgap31<+>	C57BL/6N-Arhgap31<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6461080	M	MP:0002753	dilated heart left ventricle	Arhgap40<tm1b(KOMP)Wtsi>/Arhgap40<tm1b(KOMP)Wtsi>	C57BL/6N-Arhgap40<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6461081	M	MP:0002060	abnormal skin morphology	Arih1<em1(IMPC)Tcp>/Arih1<+>	C57BL/6N-Arih1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461081	F	MP:0009142	decreased prepulse inhibition	Arih1<em1(IMPC)Tcp>/Arih1<+>	C57BL/6N-Arih1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461081	F	MP:0000157	abnormal sternum morphology	Arih1<em1(IMPC)Tcp>/Arih1<+>	C57BL/6N-Arih1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461081	M	MP:0011874	enlarged urinary bladder	Arih1<em1(IMPC)Tcp>/Arih1<+>	C57BL/6N-Arih1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461082	M	MP:0000443	abnormal snout morphology	Arl2bp<em1(IMPC)J>/Arl2bp<em1(IMPC)J>	C57BL/6NJ-Arl2bp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461082	F	MP:0010124	decreased bone mineral content	Arl2bp<em1(IMPC)J>/Arl2bp<em1(IMPC)J>	C57BL/6NJ-Arl2bp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461082	M	MP:0008259	abnormal optic disk morphology	Arl2bp<em1(IMPC)J>/Arl2bp<em1(IMPC)J>	C57BL/6NJ-Arl2bp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461083	M	MP:0000702	enlarged lymph nodes	Armcx1<em1(IMPC)Mbp>/Y	C57BL/6N-Armcx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461083	M	MP:0000266	abnormal heart morphology	Armcx1<em1(IMPC)Mbp>/Y	C57BL/6N-Armcx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461083	M	MP:0002339	abnormal lymph node morphology	Armcx1<em1(IMPC)Mbp>/Y	C57BL/6N-Armcx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461083	M	MP:0000274	enlarged heart	Armcx1<em1(IMPC)Mbp>/Y	C57BL/6N-Armcx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461086	M	MP:0005333	decreased heart rate	Arrdc2<tm1b(EUCOMM)Wtsi>/Arrdc2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arrdc2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6461086	F	MP:0011110	preweaning lethality, incomplete penetrance	Arrdc2<tm1b(EUCOMM)Wtsi>/Arrdc2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arrdc2<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6461088	F	MP:0000689	abnormal spleen morphology	Asb1<em1(IMPC)Ccpcz>/Asb1<em1(IMPC)Ccpcz>	C57BL/6N-Asb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461088	F	MP:0002060	abnormal skin morphology	Asb1<em1(IMPC)Ccpcz>/Asb1<em1(IMPC)Ccpcz>	C57BL/6N-Asb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461088	F	MP:0000691	enlarged spleen	Asb1<em1(IMPC)Ccpcz>/Asb1<em1(IMPC)Ccpcz>	C57BL/6N-Asb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461090	M	MP:0001552	increased circulating triglyceride level	Asic1<em1(IMPC)Mbp>/Asic1<em1(IMPC)Mbp>	C57BL/6N-Asic1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461090	M	MP:0001489	decreased startle reflex	Asic1<em1(IMPC)Mbp>/Asic1<em1(IMPC)Mbp>	C57BL/6N-Asic1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461091	F	MP:0020421	increased freezing behavior	Asic2<em1(IMPC)Mbp>/Asic2<em1(IMPC)Mbp>	C57BL/6N-Asic2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461091	F	MP:0002989	small kidney	Asic2<em1(IMPC)Mbp>/Asic2<em1(IMPC)Mbp>	C57BL/6N-Asic2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461091	F	MP:0002135	abnormal kidney morphology	Asic2<em1(IMPC)Mbp>/Asic2<em1(IMPC)Mbp>	C57BL/6N-Asic2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461091	M	MP:0000692	small spleen	Asic2<em1(IMPC)Mbp>/Asic2<em1(IMPC)Mbp>	C57BL/6N-Asic2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461092	F	MP:0002591	decreased mean corpuscular volume	Asxl2<tm1b(EUCOMM)Hmgu>/Asxl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Asxl2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:6461092	F	MP:0005178	increased circulating cholesterol level	Asxl2<tm1b(EUCOMM)Hmgu>/Asxl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Asxl2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:6461092	M	MP:0011110	preweaning lethality, incomplete penetrance	Asxl2<tm1b(EUCOMM)Hmgu>/Asxl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Asxl2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:6461092	F	MP:0010392	prolonged QRS complex duration	Asxl2<tm1b(EUCOMM)Hmgu>/Asxl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Asxl2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:6461092	F	MP:0001325	abnormal retina morphology	Asxl2<tm1b(EUCOMM)Hmgu>/Asxl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Asxl2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:6461092	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Asxl2<tm1b(EUCOMM)Hmgu>/Asxl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Asxl2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:6461092	F	MP:0002968	increased circulating alkaline phosphatase level	Asxl2<tm1b(EUCOMM)Hmgu>/Asxl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Asxl2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:6461092	F	MP:0010052	increased grip strength	Asxl2<tm1b(EUCOMM)Hmgu>/Asxl2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Asxl2<tm1b(EUCOMM)Hmgu>/Tcp	N	MGI:5576271
MGI:6461094	F	MP:0010579	increased heart left ventricle size	Atad5<em1(IMPC)Bay>/Atad5<+>	C57BL/6N-Atad5<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6461095	F	MP:0001417	decreased exploration in new environment	Atg2b<em1(IMPC)J>/Atg2b<em1(IMPC)J>	C57BL/6NJ-Atg2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461095	F	MP:0001325	abnormal retina morphology	Atg2b<em1(IMPC)J>/Atg2b<em1(IMPC)J>	C57BL/6NJ-Atg2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461095	F	MP:0005178	increased circulating cholesterol level	Atg2b<em1(IMPC)J>/Atg2b<em1(IMPC)J>	C57BL/6NJ-Atg2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461095	M	MP:0002833	increased heart weight	Atg2b<em1(IMPC)J>/Atg2b<em1(IMPC)J>	C57BL/6NJ-Atg2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461096	M	MP:0005561	increased mean corpuscular hemoglobin	Atp11c<em1(IMPC)J>/Y	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461096	M	MP:0001556	increased circulating HDL cholesterol level	Atp11c<em1(IMPC)J>/Y	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461096	M	MP:0000221	decreased leukocyte cell number	Atp11c<em1(IMPC)J>/Y	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461096	M	MP:0002875	decreased erythrocyte cell number	Atp11c<em1(IMPC)J>/Y	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461096	M	MP:0005278	abnormal cholesterol homeostasis	Atp11c<em1(IMPC)J>/Y	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461096	M	MP:0000208	decreased hematocrit	Atp11c<em1(IMPC)J>/Y	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461096	M	MP:0005344	increased circulating bilirubin level	Atp11c<em1(IMPC)J>/Y	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461096	M	MP:0002874	decreased hemoglobin content	Atp11c<em1(IMPC)J>/Y	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461096	M	MP:0002590	increased mean corpuscular volume	Atp11c<em1(IMPC)J>/Y	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461096	M	MP:0005178	increased circulating cholesterol level	Atp11c<em1(IMPC)J>/Y	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461098	M	MP:0002075	abnormal coat/hair pigmentation	Atp7a<em1(IMPC)J>/Y	C57BL/6NJ-Atp7a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461098	M	MP:0000367	abnormal coat/ hair morphology	Atp7a<em1(IMPC)J>/Y	C57BL/6NJ-Atp7a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461098	M	MP:0001529	abnormal vocalization	Atp7a<em1(IMPC)J>/Y	C57BL/6NJ-Atp7a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461099	F	MP:0002075	abnormal coat/hair pigmentation	Atp7a<em1(IMPC)J>/Atp7a<em1(IMPC)J>	C57BL/6NJ-Atp7a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461099	F	MP:0001529	abnormal vocalization	Atp7a<em1(IMPC)J>/Atp7a<em1(IMPC)J>	C57BL/6NJ-Atp7a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461101	F	MP:0010053	decreased grip strength	Avpr1a<em1(IMPC)J>/Avpr1a<em1(IMPC)J>	C57BL/6NJ-Avpr1a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461104	F	MP:0001417	decreased exploration in new environment	Bccip<tm1b(EUCOMM)Hmgu>/Bccip<+>	C57BL/6N-Bccip<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6461106	F	MP:0002989	small kidney	Bicc1<em1(IMPC)Mbp>/Bicc1<+>	C57BL/6N-Bicc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461106	F	MP:0001402	decreased locomotor activity	Bicc1<em1(IMPC)Mbp>/Bicc1<+>	C57BL/6N-Bicc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461106	F	MP:0002135	abnormal kidney morphology	Bicc1<em1(IMPC)Mbp>/Bicc1<+>	C57BL/6N-Bicc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461107	F	MP:0000691	enlarged spleen	Bicdl2<em1(IMPC)Mbp>/Bicdl2<em1(IMPC)Mbp>	C57BL/6N-Bicdl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461107	F	MP:0000689	abnormal spleen morphology	Bicdl2<em1(IMPC)Mbp>/Bicdl2<em1(IMPC)Mbp>	C57BL/6N-Bicdl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461107	M	MP:0002135	abnormal kidney morphology	Bicdl2<em1(IMPC)Mbp>/Bicdl2<em1(IMPC)Mbp>	C57BL/6N-Bicdl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461107	M	MP:0003068	enlarged kidney	Bicdl2<em1(IMPC)Mbp>/Bicdl2<em1(IMPC)Mbp>	C57BL/6N-Bicdl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461108	M	MP:0000219	increased neutrophil cell number	Brd9<em1(IMPC)Tcp>/Brd9<+>	C57BL/6NCrl-Brd9<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461108	F	MP:0002637	small uterus	Brd9<em1(IMPC)Tcp>/Brd9<+>	C57BL/6NCrl-Brd9<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461108	F	MP:0010124	decreased bone mineral content	Brd9<em1(IMPC)Tcp>/Brd9<+>	C57BL/6NCrl-Brd9<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461108	M	MP:0002059	abnormal seminal vesicle morphology	Brd9<em1(IMPC)Tcp>/Brd9<+>	C57BL/6NCrl-Brd9<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461108	F	MP:0002060	abnormal skin morphology	Brd9<em1(IMPC)Tcp>/Brd9<+>	C57BL/6NCrl-Brd9<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461108	M	MP:0002768	small adrenal glands	Brd9<em1(IMPC)Tcp>/Brd9<+>	C57BL/6NCrl-Brd9<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461108	M	MP:0011874	enlarged urinary bladder	Brd9<em1(IMPC)Tcp>/Brd9<+>	C57BL/6NCrl-Brd9<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461111	M	MP:0010579	increased heart left ventricle size	Btbd8<em1(IMPC)Ccpcz>/Btbd8<em1(IMPC)Ccpcz>	C57BL/6N-Btbd8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461111	M	MP:0002059	abnormal seminal vesicle morphology	Btbd8<em1(IMPC)Ccpcz>/Btbd8<em1(IMPC)Ccpcz>	C57BL/6N-Btbd8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461111	F	MP:0002060	abnormal skin morphology	Btbd8<em1(IMPC)Ccpcz>/Btbd8<em1(IMPC)Ccpcz>	C57BL/6N-Btbd8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461112	F	MP:0005016	decreased lymphocyte cell number	Btg1<em1(IMPC)Mbp>/Btg1<em1(IMPC)Mbp>	C57BL/6NCrl-Btg1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461112	M	MP:0003068	enlarged kidney	Btg1<em1(IMPC)Mbp>/Btg1<em1(IMPC)Mbp>	C57BL/6NCrl-Btg1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461112	F	MP:0001126	abnormal ovary morphology	Btg1<em1(IMPC)Mbp>/Btg1<em1(IMPC)Mbp>	C57BL/6NCrl-Btg1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461112	F	MP:0000691	enlarged spleen	Btg1<em1(IMPC)Mbp>/Btg1<em1(IMPC)Mbp>	C57BL/6NCrl-Btg1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461112	F	MP:0004906	enlarged uterus	Btg1<em1(IMPC)Mbp>/Btg1<em1(IMPC)Mbp>	C57BL/6NCrl-Btg1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461112	F	MP:0002590	increased mean corpuscular volume	Btg1<em1(IMPC)Mbp>/Btg1<em1(IMPC)Mbp>	C57BL/6NCrl-Btg1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461112	F	MP:0004832	enlarged ovary	Btg1<em1(IMPC)Mbp>/Btg1<em1(IMPC)Mbp>	C57BL/6NCrl-Btg1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461112	M	MP:0002060	abnormal skin morphology	Btg1<em1(IMPC)Mbp>/Btg1<em1(IMPC)Mbp>	C57BL/6NCrl-Btg1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461112	F	MP:0001120	abnormal uterus morphology	Btg1<em1(IMPC)Mbp>/Btg1<em1(IMPC)Mbp>	C57BL/6NCrl-Btg1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461113	M	MP:0003642	absent seminal vesicle	C1qtnf12<em1(IMPC)Mbp>/C1qtnf12<em1(IMPC)Mbp>	C57BL/6NCrl-C1qtnf12<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461113	M	MP:0002997	enlarged seminal vesicle	C1qtnf12<em1(IMPC)Mbp>/C1qtnf12<em1(IMPC)Mbp>	C57BL/6NCrl-C1qtnf12<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461113	M	MP:0002092	abnormal eye morphology	C1qtnf12<em1(IMPC)Mbp>/C1qtnf12<em1(IMPC)Mbp>	C57BL/6NCrl-C1qtnf12<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461113	M	MP:0001293	anophthalmia	C1qtnf12<em1(IMPC)Mbp>/C1qtnf12<em1(IMPC)Mbp>	C57BL/6NCrl-C1qtnf12<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461113	F	MP:0001297	microphthalmia	C1qtnf12<em1(IMPC)Mbp>/C1qtnf12<em1(IMPC)Mbp>	C57BL/6NCrl-C1qtnf12<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461114	M	MP:0000702	enlarged lymph nodes	C1qtnf1<em1(IMPC)Mbp>/C1qtnf1<em1(IMPC)Mbp>	C57BL/6N-C1qtnf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461114	F	MP:0002989	small kidney	C1qtnf1<em1(IMPC)Mbp>/C1qtnf1<em1(IMPC)Mbp>	C57BL/6N-C1qtnf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461114	F	MP:0001126	abnormal ovary morphology	C1qtnf1<em1(IMPC)Mbp>/C1qtnf1<em1(IMPC)Mbp>	C57BL/6N-C1qtnf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461114	F	MP:0009476	enlarged cecum	C1qtnf1<em1(IMPC)Mbp>/C1qtnf1<em1(IMPC)Mbp>	C57BL/6N-C1qtnf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461114	F	MP:0001297	microphthalmia	C1qtnf1<em1(IMPC)Mbp>/C1qtnf1<em1(IMPC)Mbp>	C57BL/6N-C1qtnf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461114	M	MP:0000186	decreased circulating HDL cholesterol level	C1qtnf1<em1(IMPC)Mbp>/C1qtnf1<em1(IMPC)Mbp>	C57BL/6N-C1qtnf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461114	M	MP:0002644	decreased circulating triglyceride level	C1qtnf1<em1(IMPC)Mbp>/C1qtnf1<em1(IMPC)Mbp>	C57BL/6N-C1qtnf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461114	M	MP:0000598	abnormal liver morphology	C1qtnf1<em1(IMPC)Mbp>/C1qtnf1<em1(IMPC)Mbp>	C57BL/6N-C1qtnf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461114	F	MP:0002060	abnormal skin morphology	C1qtnf1<em1(IMPC)Mbp>/C1qtnf1<em1(IMPC)Mbp>	C57BL/6N-C1qtnf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461114	M	MP:0002339	abnormal lymph node morphology	C1qtnf1<em1(IMPC)Mbp>/C1qtnf1<em1(IMPC)Mbp>	C57BL/6N-C1qtnf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461114	M	MP:0005179	decreased circulating cholesterol level	C1qtnf1<em1(IMPC)Mbp>/C1qtnf1<em1(IMPC)Mbp>	C57BL/6N-C1qtnf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461114	F	MP:0000494	abnormal cecum morphology	C1qtnf1<em1(IMPC)Mbp>/C1qtnf1<em1(IMPC)Mbp>	C57BL/6N-C1qtnf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461114	M	MP:0001402	decreased locomotor activity	C1qtnf1<em1(IMPC)Mbp>/C1qtnf1<em1(IMPC)Mbp>	C57BL/6N-C1qtnf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461115	M	MP:0001399	hyperactivity	C2cd3<em1(IMPC)Tcp>/C2cd3<+>	C57BL/6N-C2cd3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461115	F	MP:0001120	abnormal uterus morphology	C2cd3<em1(IMPC)Tcp>/C2cd3<+>	C57BL/6N-C2cd3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461115	M	MP:0011874	enlarged urinary bladder	C2cd3<em1(IMPC)Tcp>/C2cd3<+>	C57BL/6N-C2cd3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461115	M	MP:0002060	abnormal skin morphology	C2cd3<em1(IMPC)Tcp>/C2cd3<+>	C57BL/6N-C2cd3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461115	F	MP:0000219	increased neutrophil cell number	C2cd3<em1(IMPC)Tcp>/C2cd3<+>	C57BL/6N-C2cd3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461115	F	MP:0005016	decreased lymphocyte cell number	C2cd3<em1(IMPC)Tcp>/C2cd3<+>	C57BL/6N-C2cd3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461116	M	MP:0003961	decreased lean body mass	C4b<em1(IMPC)H>/C4b<em1(IMPC)H>	C57BL/6NTac-C4b<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461116	M	MP:0020421	increased freezing behavior	C4b<em1(IMPC)H>/C4b<em1(IMPC)H>	C57BL/6NTac-C4b<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461117	M	MP:0001489	decreased startle reflex	Cabp2<em1(IMPC)J>/Cabp2<em1(IMPC)J>	C57BL/6NJ-Cabp2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461117	F	MP:0010053	decreased grip strength	Cabp2<em1(IMPC)J>/Cabp2<em1(IMPC)J>	C57BL/6NJ-Cabp2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461118	F	MP:0010053	decreased grip strength	Cachd1<em1(IMPC)J>/Cachd1<+>	C57BL/6NJ-Cachd1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461120	M	MP:0001486	abnormal startle reflex	Calcoco1<em1(IMPC)H>/Calcoco1<em1(IMPC)H>	C57BL/6N-Calcoco1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461120	M	MP:0011874	enlarged urinary bladder	Calcoco1<em1(IMPC)H>/Calcoco1<em1(IMPC)H>	C57BL/6N-Calcoco1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461120	M	MP:0003068	enlarged kidney	Calcoco1<em1(IMPC)H>/Calcoco1<em1(IMPC)H>	C57BL/6N-Calcoco1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461120	F	MP:0001325	abnormal retina morphology	Calcoco1<em1(IMPC)H>/Calcoco1<em1(IMPC)H>	C57BL/6N-Calcoco1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461120	F	MP:0005567	decreased circulating total protein level	Calcoco1<em1(IMPC)H>/Calcoco1<em1(IMPC)H>	C57BL/6N-Calcoco1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461120	M	MP:0001392	abnormal locomotor behavior	Calcoco1<em1(IMPC)H>/Calcoco1<em1(IMPC)H>	C57BL/6N-Calcoco1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461120	M	MP:0000198	decreased circulating phosphate level	Calcoco1<em1(IMPC)H>/Calcoco1<em1(IMPC)H>	C57BL/6N-Calcoco1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461121	M	MP:0000841	abnormal hindbrain morphology	Calu<em1(IMPC)Tcp>/Calu<em1(IMPC)Tcp>	C57BL/6N-Calu<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461121	M	MP:0000897	abnormal midbrain morphology	Calu<em1(IMPC)Tcp>/Calu<em1(IMPC)Tcp>	C57BL/6N-Calu<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461121	M	MP:0003257	abnormal abdominal wall morphology	Calu<em1(IMPC)Tcp>/Calu<em1(IMPC)Tcp>	C57BL/6N-Calu<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461122	F	MP:0009453	enhanced contextual conditioning behavior	Cartpt<em1(IMPC)Mbp>/Cartpt<em1(IMPC)Mbp>	C57BL/6N-Cartpt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461122	F	MP:0002989	small kidney	Cartpt<em1(IMPC)Mbp>/Cartpt<em1(IMPC)Mbp>	C57BL/6N-Cartpt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461122	F	MP:0000266	abnormal heart morphology	Cartpt<em1(IMPC)Mbp>/Cartpt<em1(IMPC)Mbp>	C57BL/6N-Cartpt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461122	F	MP:0001417	decreased exploration in new environment	Cartpt<em1(IMPC)Mbp>/Cartpt<em1(IMPC)Mbp>	C57BL/6N-Cartpt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461122	M	MP:0001488	increased startle reflex	Cartpt<em1(IMPC)Mbp>/Cartpt<em1(IMPC)Mbp>	C57BL/6N-Cartpt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461122	M	MP:0000494	abnormal cecum morphology	Cartpt<em1(IMPC)Mbp>/Cartpt<em1(IMPC)Mbp>	C57BL/6N-Cartpt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461122	F	MP:0002135	abnormal kidney morphology	Cartpt<em1(IMPC)Mbp>/Cartpt<em1(IMPC)Mbp>	C57BL/6N-Cartpt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461122	F	MP:0002188	small heart	Cartpt<em1(IMPC)Mbp>/Cartpt<em1(IMPC)Mbp>	C57BL/6N-Cartpt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461123	M	MP:0005576	decreased pulmonary ventilation	Casp4<tm1b(KOMP)Wtsi>/Casp4<tm1b(KOMP)Wtsi>	C57BL/6N-Casp4<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6461125	M	MP:0005564	increased hemoglobin content	Cav1<em2(IMPC)Ics>/Cav1<em2(IMPC)Ics>	C57BL/6N-Cav1<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461125	F	MP:0002626	increased heart rate	Cav1<em2(IMPC)Ics>/Cav1<em2(IMPC)Ics>	C57BL/6N-Cav1<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461125	M	MP:0005561	increased mean corpuscular hemoglobin	Cav1<em2(IMPC)Ics>/Cav1<em2(IMPC)Ics>	C57BL/6N-Cav1<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461125	M	MP:0005178	increased circulating cholesterol level	Cav1<em2(IMPC)Ics>/Cav1<em2(IMPC)Ics>	C57BL/6N-Cav1<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461125	F	MP:0010053	decreased grip strength	Cav1<em2(IMPC)Ics>/Cav1<em2(IMPC)Ics>	C57BL/6N-Cav1<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461125	M	MP:0002590	increased mean corpuscular volume	Cav1<em2(IMPC)Ics>/Cav1<em2(IMPC)Ics>	C57BL/6N-Cav1<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461125	M	MP:0001556	increased circulating HDL cholesterol level	Cav1<em2(IMPC)Ics>/Cav1<em2(IMPC)Ics>	C57BL/6N-Cav1<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461128	F	MP:0002092	abnormal eye morphology	Ccdc186<em1(IMPC)Mbp>/Ccdc186<+>	C57BL/6NCrl-Ccdc186<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461129	M	MP:0005293	impaired glucose tolerance	Ccdc25<em1(IMPC)Mbp>/Ccdc25<+>	C57BL/6N-Ccdc25<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461129	F	MP:0001333	absent optic nerve	Ccdc25<em1(IMPC)Mbp>/Ccdc25<+>	C57BL/6N-Ccdc25<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461130	F	MP:0001364	decreased anxiety-related response	Ccr8<em1(IMPC)Mbp>/Ccr8<em1(IMPC)Mbp>	C57BL/6N-Ccr8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461130	F	MP:0020870	decreased thigmotaxis	Ccr8<em1(IMPC)Mbp>/Ccr8<em1(IMPC)Mbp>	C57BL/6N-Ccr8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461130	F	MP:0004924	abnormal behavior	Ccr8<em1(IMPC)Mbp>/Ccr8<em1(IMPC)Mbp>	C57BL/6N-Ccr8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461130	F	MP:0001402	decreased locomotor activity	Ccr8<em1(IMPC)Mbp>/Ccr8<em1(IMPC)Mbp>	C57BL/6N-Ccr8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461130	F	MP:0002092	abnormal eye morphology	Ccr8<em1(IMPC)Mbp>/Ccr8<em1(IMPC)Mbp>	C57BL/6N-Ccr8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461130	F	MP:0009084	blind uterus	Ccr8<em1(IMPC)Mbp>/Ccr8<em1(IMPC)Mbp>	C57BL/6N-Ccr8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461132	M	MP:0000218	increased leukocyte cell number	Cd96<em1(IMPC)Wtsi>/Cd96<em1(IMPC)Wtsi>	C57BL/6N-Cd96<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:6461133	F	MP:0001304	cataract	Cdc14a<tm1e.1(EUCOMM)Hmgu>/Cdc14a<+>	B6N(Cg)-Cdc14a<tm1e.1(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461136	F	MP:0003900	shortened QT interval	Cdh13<tm1b(EUCOMM)Hmgu>/Cdh13<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cdh13<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461136	F	MP:0001399	hyperactivity	Cdh13<tm1b(EUCOMM)Hmgu>/Cdh13<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cdh13<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461136	M	MP:0010053	decreased grip strength	Cdh13<tm1b(EUCOMM)Hmgu>/Cdh13<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cdh13<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461137	F	MP:0005576	decreased pulmonary ventilation	Cdh26<tm1.1(KOMP)Vlcg>/Cdh26<tm1.1(KOMP)Vlcg>	C57BL/6N-Cdh26<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461137	F	MP:0005575	increased pulmonary ventilation	Cdh26<tm1.1(KOMP)Vlcg>/Cdh26<tm1.1(KOMP)Vlcg>	C57BL/6N-Cdh26<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461137	F	MP:0005586	decreased tidal volume	Cdh26<tm1.1(KOMP)Vlcg>/Cdh26<tm1.1(KOMP)Vlcg>	C57BL/6N-Cdh26<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461138	M	MP:0005178	increased circulating cholesterol level	Cdh9<tm1b(KOMP)Wtsi>/Cdh9<tm1b(KOMP)Wtsi>	C57BL/6N-Cdh9<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6461138	F	MP:0010053	decreased grip strength	Cdh9<tm1b(KOMP)Wtsi>/Cdh9<tm1b(KOMP)Wtsi>	C57BL/6N-Cdh9<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6461139	M	MP:0002702	decreased circulating free fatty acids level	Cdk15<tm1b(KOMP)Wtsi>/Cdk15<tm1b(KOMP)Wtsi>	B6N(Cg)-Cdk15<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461139	M	MP:0002833	increased heart weight	Cdk15<tm1b(KOMP)Wtsi>/Cdk15<tm1b(KOMP)Wtsi>	B6N(Cg)-Cdk15<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461141	F	MP:0001304	cataract	Cdkl4<tm1.1(KOMP)Vlcg>/Cdkl4<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cdkl4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461141	F	MP:0002968	increased circulating alkaline phosphatase level	Cdkl4<tm1.1(KOMP)Vlcg>/Cdkl4<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cdkl4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461142	M	MP:0002599	increased mean platelet volume	Ceacam5<em1(IMPC)Wtsi>/Ceacam5<em1(IMPC)Wtsi>	C57BL/6N-Ceacam5<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461142	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Ceacam5<em1(IMPC)Wtsi>/Ceacam5<em1(IMPC)Wtsi>	C57BL/6N-Ceacam5<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461142	M	MP:0000218	increased leukocyte cell number	Ceacam5<em1(IMPC)Wtsi>/Ceacam5<em1(IMPC)Wtsi>	C57BL/6N-Ceacam5<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461143	F	MP:0010053	decreased grip strength	Cep350<em1(IMPC)J>/Cep350<em1(IMPC)J>	C57BL/6NJ-Cep350<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461144	M	MP:0013279	increased fasting circulating glucose level	Cep57l1<tm1b(KOMP)Wtsi>/Cep57l1<+>	B6N(Cg)-Cep57l1<tm1b(KOMP)Wtsi>/2J	N	MGI:5576271
MGI:6461145	F	MP:0000274	enlarged heart	Cep83<tm1.1(KOMP)Vlcg>/Cep83<+>	C57BL/6N-Cep83<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6461145	F	MP:0009709	hydrometra	Cep83<tm1.1(KOMP)Vlcg>/Cep83<+>	C57BL/6N-Cep83<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6461145	F	MP:0000266	abnormal heart morphology	Cep83<tm1.1(KOMP)Vlcg>/Cep83<+>	C57BL/6N-Cep83<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6461145	F	MP:0001102	small superior vagus ganglion	Cep83<tm1.1(KOMP)Vlcg>/Cep83<+>	C57BL/6N-Cep83<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6461146	F	MP:0004924	abnormal behavior	Cep95<em1(IMPC)J>/Cep95<em1(IMPC)J>	C57BL/6NJ-Cep95<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461146	F	MP:0020870	decreased thigmotaxis	Cep95<em1(IMPC)J>/Cep95<em1(IMPC)J>	C57BL/6NJ-Cep95<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461148	F	MP:0005627	increased circulating potassium level	Chchd10<em1(IMPC)H>/Chchd10<em1(IMPC)H>	C57BL/6N-Chchd10<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461148	F	MP:0005553	increased circulating creatinine level	Chchd10<em1(IMPC)H>/Chchd10<em1(IMPC)H>	C57BL/6N-Chchd10<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461148	F	MP:0010052	increased grip strength	Chchd10<em1(IMPC)H>/Chchd10<em1(IMPC)H>	C57BL/6N-Chchd10<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461148	F	MP:0005565	increased blood urea nitrogen level	Chchd10<em1(IMPC)H>/Chchd10<em1(IMPC)H>	C57BL/6N-Chchd10<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461150	M	MP:0002607	decreased basophil cell number	Chmp4c<tm1b(EUCOMM)Wtsi>/Chmp4c<tm1b(EUCOMM)Wtsi>	C57BL/6N-Chmp4c<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6461150	M	MP:0002941	increased circulating alanine transaminase level	Chmp4c<tm1b(EUCOMM)Wtsi>/Chmp4c<tm1b(EUCOMM)Wtsi>	C57BL/6N-Chmp4c<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6461151	M	MP:0001697	abnormal embryo size	Chmp7<em1(IMPC)J>/Chmp7<+>	C57BL/6NJ-Chmp7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461153	F	MP:0001297	microphthalmia	Chst2<em1(IMPC)Mbp>/Chst2<em1(IMPC)Mbp>	C57BL/6N-Chst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461153	F	MP:0001120	abnormal uterus morphology	Chst2<em1(IMPC)Mbp>/Chst2<em1(IMPC)Mbp>	C57BL/6N-Chst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461153	M	MP:0000274	enlarged heart	Chst2<em1(IMPC)Mbp>/Chst2<em1(IMPC)Mbp>	C57BL/6N-Chst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461153	M	MP:0010053	decreased grip strength	Chst2<em1(IMPC)Mbp>/Chst2<em1(IMPC)Mbp>	C57BL/6N-Chst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461153	F	MP:0002989	small kidney	Chst2<em1(IMPC)Mbp>/Chst2<em1(IMPC)Mbp>	C57BL/6N-Chst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461153	F	MP:0005343	increased circulating aspartate transaminase level	Chst2<em1(IMPC)Mbp>/Chst2<em1(IMPC)Mbp>	C57BL/6N-Chst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461153	M	MP:0002092	abnormal eye morphology	Chst2<em1(IMPC)Mbp>/Chst2<em1(IMPC)Mbp>	C57BL/6N-Chst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461153	F	MP:0009709	hydrometra	Chst2<em1(IMPC)Mbp>/Chst2<em1(IMPC)Mbp>	C57BL/6N-Chst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461153	F	MP:0000709	enlarged thymus	Chst2<em1(IMPC)Mbp>/Chst2<em1(IMPC)Mbp>	C57BL/6N-Chst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461153	M	MP:0000598	abnormal liver morphology	Chst2<em1(IMPC)Mbp>/Chst2<em1(IMPC)Mbp>	C57BL/6N-Chst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461153	M	MP:0000599	enlarged liver	Chst2<em1(IMPC)Mbp>/Chst2<em1(IMPC)Mbp>	C57BL/6N-Chst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461153	F	MP:0000703	abnormal thymus morphology	Chst2<em1(IMPC)Mbp>/Chst2<em1(IMPC)Mbp>	C57BL/6N-Chst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461154	M	MP:0001146	abnormal testis morphology	Clasp1<em1(IMPC)Mbp>/Clasp1<+>	C57BL/6NCrl-Clasp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461154	F	MP:0009709	hydrometra	Clasp1<em1(IMPC)Mbp>/Clasp1<+>	C57BL/6NCrl-Clasp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461154	F	MP:0009084	blind uterus	Clasp1<em1(IMPC)Mbp>/Clasp1<+>	C57BL/6NCrl-Clasp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461154	F	MP:0001399	hyperactivity	Clasp1<em1(IMPC)Mbp>/Clasp1<+>	C57BL/6NCrl-Clasp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461154	M	MP:0003642	absent seminal vesicle	Clasp1<em1(IMPC)Mbp>/Clasp1<+>	C57BL/6NCrl-Clasp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461154	F	MP:0000702	enlarged lymph nodes	Clasp1<em1(IMPC)Mbp>/Clasp1<+>	C57BL/6NCrl-Clasp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461154	M	MP:0004931	enlarged epididymis	Clasp1<em1(IMPC)Mbp>/Clasp1<+>	C57BL/6NCrl-Clasp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461154	F	MP:0000599	enlarged liver	Clasp1<em1(IMPC)Mbp>/Clasp1<+>	C57BL/6NCrl-Clasp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461154	M	MP:0002997	enlarged seminal vesicle	Clasp1<em1(IMPC)Mbp>/Clasp1<+>	C57BL/6NCrl-Clasp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461154	F	MP:0002188	small heart	Clasp1<em1(IMPC)Mbp>/Clasp1<+>	C57BL/6NCrl-Clasp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461154	M	MP:0001147	small testis	Clasp1<em1(IMPC)Mbp>/Clasp1<+>	C57BL/6NCrl-Clasp1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461155	F	MP:0001325	abnormal retina morphology	Cldn1<tm1b(NCOM)Mfgc>/Cldn1<+>	C57BL/6N-Cldn1<tm1b(NCOM)Mfgc>/Tcp	N	MGI:5576271
MGI:6461156	M	MP:0011962	increased cornea thickness	Cldnd2<tm1b(EUCOMM)Hmgu>/Cldnd2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cldnd2<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6461156	F	MP:0013279	increased fasting circulating glucose level	Cldnd2<tm1b(EUCOMM)Hmgu>/Cldnd2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cldnd2<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6461156	M	MP:0002965	increased circulating serum albumin level	Cldnd2<tm1b(EUCOMM)Hmgu>/Cldnd2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cldnd2<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6461157	M	MP:0009142	decreased prepulse inhibition	Clk2<em1(IMPC)Bay>/Clk2<em1(IMPC)Bay>	C57BL/6N-Clk2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461158	F	MP:0002135	abnormal kidney morphology	Cln8<em1(IMPC)Mbp>/Cln8<em1(IMPC)Mbp>	C57BL/6N-Cln8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461158	F	MP:0000598	abnormal liver morphology	Cln8<em1(IMPC)Mbp>/Cln8<em1(IMPC)Mbp>	C57BL/6N-Cln8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461158	F	MP:0001325	abnormal retina morphology	Cln8<em1(IMPC)Mbp>/Cln8<em1(IMPC)Mbp>	C57BL/6N-Cln8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461158	F	MP:0002833	increased heart weight	Cln8<em1(IMPC)Mbp>/Cln8<em1(IMPC)Mbp>	C57BL/6N-Cln8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461158	M	MP:0001304	cataract	Cln8<em1(IMPC)Mbp>/Cln8<em1(IMPC)Mbp>	C57BL/6N-Cln8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461158	F	MP:0003068	enlarged kidney	Cln8<em1(IMPC)Mbp>/Cln8<em1(IMPC)Mbp>	C57BL/6N-Cln8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461158	F	MP:0001566	increased circulating phosphate level	Cln8<em1(IMPC)Mbp>/Cln8<em1(IMPC)Mbp>	C57BL/6N-Cln8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461158	F	MP:0000601	small liver	Cln8<em1(IMPC)Mbp>/Cln8<em1(IMPC)Mbp>	C57BL/6N-Cln8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461160	M	MP:0002833	increased heart weight	Cmtr1<em1(IMPC)J>/Cmtr1<+>	C57BL/6NJ-Cmtr1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461161	M	MP:0010025	decreased total body fat amount	Cmtr2<tm1.1(KOMP)Vlcg>/Cmtr2<+>	B6N(Cg)-Cmtr2<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:6461161	M	MP:0003960	increased lean body mass	Cmtr2<tm1.1(KOMP)Vlcg>/Cmtr2<+>	B6N(Cg)-Cmtr2<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:6461161	M	MP:0002833	increased heart weight	Cmtr2<tm1.1(KOMP)Vlcg>/Cmtr2<+>	B6N(Cg)-Cmtr2<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:6461161	F	MP:0005554	decreased circulating creatinine level	Cmtr2<tm1.1(KOMP)Vlcg>/Cmtr2<+>	B6N(Cg)-Cmtr2<tm1.1(KOMP)Vlcg>/2J	N	MGI:5576271
MGI:6461162	M	MP:0010507	shortened RR interval	Cmya5<em1(IMPC)J>/Cmya5<em1(IMPC)J>	C57BL/6NJ-Cmya5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461162	M	MP:0002626	increased heart rate	Cmya5<em1(IMPC)J>/Cmya5<em1(IMPC)J>	C57BL/6NJ-Cmya5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461163	M	MP:0000063	decreased bone mineral density	Cnep1r1<em1(IMPC)J>/Cnep1r1<+>	C57BL/6NJ-Cnep1r1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461165	M	MP:0001147	small testis	Cnpy2<em1(IMPC)Wtsi>/Cnpy2<+>	C57BL/6N-Cnpy2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461165	F	MP:0002092	abnormal eye morphology	Cnpy2<em1(IMPC)Wtsi>/Cnpy2<+>	C57BL/6N-Cnpy2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461165	M	MP:0001146	abnormal testis morphology	Cnpy2<em1(IMPC)Wtsi>/Cnpy2<+>	C57BL/6N-Cnpy2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461165	F	MP:0002932	abnormal joint morphology	Cnpy2<em1(IMPC)Wtsi>/Cnpy2<+>	C57BL/6N-Cnpy2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461165	M	MP:0013772	increased effector memory T-helper cell number	Cnpy2<em1(IMPC)Wtsi>/Cnpy2<+>	C57BL/6N-Cnpy2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461166	M	MP:0001146	abnormal testis morphology	Cnpy2<em1(IMPC)Wtsi>/Cnpy2<em1(IMPC)Wtsi>	C57BL/6N-Cnpy2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461166	M	MP:0001147	small testis	Cnpy2<em1(IMPC)Wtsi>/Cnpy2<em1(IMPC)Wtsi>	C57BL/6N-Cnpy2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461166	M	MP:0000438	abnormal cranium morphology	Cnpy2<em1(IMPC)Wtsi>/Cnpy2<em1(IMPC)Wtsi>	C57BL/6N-Cnpy2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461166	F	MP:0000137	abnormal vertebrae morphology	Cnpy2<em1(IMPC)Wtsi>/Cnpy2<em1(IMPC)Wtsi>	C57BL/6N-Cnpy2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461168	F	MP:0005544	cornea deposits	Cog7<tm1b(EUCOMM)Hmgu>/Cog7<+>	B6N(Cg)-Cog7<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461168	F	MP:0006243	impaired pupillary reflex	Cog7<tm1b(EUCOMM)Hmgu>/Cog7<+>	B6N(Cg)-Cog7<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461168	F	MP:0004122	abnormal sinus arrhythmia	Cog7<tm1b(EUCOMM)Hmgu>/Cog7<+>	B6N(Cg)-Cog7<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461169	M	MP:0010579	increased heart left ventricle size	Col11a1<em1(IMPC)Bay>/Col11a1<+>	C57BL/6N-Col11a1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461170	F	MP:0000689	abnormal spleen morphology	Col27a1<em1(IMPC)Mbp>/Col27a1<+>	C57BL/6N-Col27a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461170	M	MP:0000692	small spleen	Col27a1<em1(IMPC)Mbp>/Col27a1<+>	C57BL/6N-Col27a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461170	F	MP:0009084	blind uterus	Col27a1<em1(IMPC)Mbp>/Col27a1<+>	C57BL/6N-Col27a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461170	M	MP:0003068	enlarged kidney	Col27a1<em1(IMPC)Mbp>/Col27a1<+>	C57BL/6N-Col27a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461170	M	MP:0002135	abnormal kidney morphology	Col27a1<em1(IMPC)Mbp>/Col27a1<+>	C57BL/6N-Col27a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461171	M	MP:0001392	abnormal locomotor behavior	Coq3<em1(IMPC)J>/Coq3<+>	C57BL/6NJ-Coq3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461173	M	MP:0009142	decreased prepulse inhibition	Cox18<em1(IMPC)J>/Cox18<+>	C57BL/6NJ-Cox18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461175	M	MP:0002875	decreased erythrocyte cell number	Crabp2<em1(IMPC)Mbp>/Crabp2<em1(IMPC)Mbp>	C57BL/6N-Crabp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461175	M	MP:0000266	abnormal heart morphology	Crabp2<em1(IMPC)Mbp>/Crabp2<em1(IMPC)Mbp>	C57BL/6N-Crabp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461175	M	MP:0002833	increased heart weight	Crabp2<em1(IMPC)Mbp>/Crabp2<em1(IMPC)Mbp>	C57BL/6N-Crabp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461175	M	MP:0000274	enlarged heart	Crabp2<em1(IMPC)Mbp>/Crabp2<em1(IMPC)Mbp>	C57BL/6N-Crabp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461177	F	MP:0010123	increased bone mineral content	Cramp1<em1(IMPC)Bay>/Cramp1<+>	C57BL/6N-Cramp1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461177	F	MP:0009142	decreased prepulse inhibition	Cramp1<em1(IMPC)Bay>/Cramp1<+>	C57BL/6N-Cramp1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461177	F	MP:0003795	abnormal bone structure	Cramp1<em1(IMPC)Bay>/Cramp1<+>	C57BL/6N-Cramp1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461178	F	MP:0001513	limb grasping	Crcp<em1(IMPC)J>/Crcp<+>	C57BL/6NJ-Crcp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461178	M	MP:0000432	abnormal head morphology	Crcp<em1(IMPC)J>/Crcp<+>	C57BL/6NJ-Crcp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461181	F	MP:0001120	abnormal uterus morphology	Crlf2<em1(IMPC)Mbp>/Crlf2<em1(IMPC)Mbp>	C57BL/6N-Crlf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461181	M	MP:0003068	enlarged kidney	Crlf2<em1(IMPC)Mbp>/Crlf2<em1(IMPC)Mbp>	C57BL/6N-Crlf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461181	M	MP:0000274	enlarged heart	Crlf2<em1(IMPC)Mbp>/Crlf2<em1(IMPC)Mbp>	C57BL/6N-Crlf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461181	M	MP:0002152	abnormal brain morphology	Crlf2<em1(IMPC)Mbp>/Crlf2<em1(IMPC)Mbp>	C57BL/6N-Crlf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461181	F	MP:0005344	increased circulating bilirubin level	Crlf2<em1(IMPC)Mbp>/Crlf2<em1(IMPC)Mbp>	C57BL/6N-Crlf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461181	F	MP:0020421	increased freezing behavior	Crlf2<em1(IMPC)Mbp>/Crlf2<em1(IMPC)Mbp>	C57BL/6N-Crlf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461181	F	MP:0002989	small kidney	Crlf2<em1(IMPC)Mbp>/Crlf2<em1(IMPC)Mbp>	C57BL/6N-Crlf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461181	M	MP:0002590	increased mean corpuscular volume	Crlf2<em1(IMPC)Mbp>/Crlf2<em1(IMPC)Mbp>	C57BL/6N-Crlf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461181	F	MP:0002188	small heart	Crlf2<em1(IMPC)Mbp>/Crlf2<em1(IMPC)Mbp>	C57BL/6N-Crlf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461183	M	MP:0002075	abnormal coat/hair pigmentation	Cspp1<em1(IMPC)J>/Cspp1<em1(IMPC)J>	C57BL/6NJ-Cspp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461183	M	MP:0005554	decreased circulating creatinine level	Cspp1<em1(IMPC)J>/Cspp1<em1(IMPC)J>	C57BL/6NJ-Cspp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461183	M	MP:0001529	abnormal vocalization	Cspp1<em1(IMPC)J>/Cspp1<em1(IMPC)J>	C57BL/6NJ-Cspp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461183	F	MP:0001392	abnormal locomotor behavior	Cspp1<em1(IMPC)J>/Cspp1<em1(IMPC)J>	C57BL/6NJ-Cspp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461184	F	MP:0005293	impaired glucose tolerance	Ctbs<em1(IMPC)J>/Ctbs<em1(IMPC)J>	C57BL/6NJ-Ctbs<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461186	F	MP:0000208	decreased hematocrit	Cuedc1<em1(IMPC)J>/Cuedc1<em1(IMPC)J>	C57BL/6NJ-Cuedc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461186	F	MP:0002875	decreased erythrocyte cell number	Cuedc1<em1(IMPC)J>/Cuedc1<em1(IMPC)J>	C57BL/6NJ-Cuedc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461186	M	MP:0001489	decreased startle reflex	Cuedc1<em1(IMPC)J>/Cuedc1<em1(IMPC)J>	C57BL/6NJ-Cuedc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461186	F	MP:0002591	decreased mean corpuscular volume	Cuedc1<em1(IMPC)J>/Cuedc1<em1(IMPC)J>	C57BL/6NJ-Cuedc1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461187	F	MP:0000692	small spleen	Cxadr<em1(IMPC)Mbp>/Cxadr<+>	C57BL/6N-Cxadr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461187	M	MP:0000470	abnormal stomach morphology	Cxadr<em1(IMPC)Mbp>/Cxadr<+>	C57BL/6N-Cxadr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461187	M	MP:0000689	abnormal spleen morphology	Cxadr<em1(IMPC)Mbp>/Cxadr<+>	C57BL/6N-Cxadr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461187	M	MP:0000598	abnormal liver morphology	Cxadr<em1(IMPC)Mbp>/Cxadr<+>	C57BL/6N-Cxadr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461187	F	MP:0002989	small kidney	Cxadr<em1(IMPC)Mbp>/Cxadr<+>	C57BL/6N-Cxadr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461187	F	MP:0002135	abnormal kidney morphology	Cxadr<em1(IMPC)Mbp>/Cxadr<+>	C57BL/6N-Cxadr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461188	M	MP:0005561	increased mean corpuscular hemoglobin	Cyp2c23<tm1b(EUCOMM)Hmgu>/Cyp2c23<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp2c23<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461188	M	MP:0002968	increased circulating alkaline phosphatase level	Cyp2c23<tm1b(EUCOMM)Hmgu>/Cyp2c23<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp2c23<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461188	M	MP:0005178	increased circulating cholesterol level	Cyp2c23<tm1b(EUCOMM)Hmgu>/Cyp2c23<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp2c23<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461189	M	MP:0000599	enlarged liver	Cyp4v3<em1(IMPC)Mbp>/Cyp4v3<em1(IMPC)Mbp>	C57BL/6NCrl-Cyp4v3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461189	F	MP:0002092	abnormal eye morphology	Cyp4v3<em1(IMPC)Mbp>/Cyp4v3<em1(IMPC)Mbp>	C57BL/6NCrl-Cyp4v3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461189	M	MP:0001399	hyperactivity	Cyp4v3<em1(IMPC)Mbp>/Cyp4v3<em1(IMPC)Mbp>	C57BL/6NCrl-Cyp4v3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461190	F	MP:0002591	decreased mean corpuscular volume	D16Ertd472e<tm1b(EUCOMM)Wtsi>/D16Ertd472e<tm1b(EUCOMM)Wtsi>	C57BL/6N-D16Ertd472e<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6461191	M	MP:0003179	thrombocytopenia	D5Ertd579e<em1(IMPC)J>/D5Ertd579e<em1(IMPC)J>	C57BL/6NJ-D5Ertd579e<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461192	M	MP:0020870	decreased thigmotaxis	Dalrd3<em1(IMPC)J>/Dalrd3<em1(IMPC)J>	C57BL/6NJ-Dalrd3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461196	M	MP:0002608	increased hematocrit	Dcdc2b<tm1b(KOMP)Wtsi>/Dcdc2b<tm1b(KOMP)Wtsi>	C57BL/6N-Dcdc2b<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461196	M	MP:0003131	increased erythrocyte cell number	Dcdc2b<tm1b(KOMP)Wtsi>/Dcdc2b<tm1b(KOMP)Wtsi>	C57BL/6N-Dcdc2b<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461198	F	MP:0001399	hyperactivity	Ddr1<tm1b(EUCOMM)Hmgu>/Ddr1<+>	C57BL/6N-Ddr1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6461199	F	MP:0000639	abnormal adrenal gland morphology	Ddx24<em1(IMPC)Mbp>/Ddx24<+>	C57BL/6NCrl-Ddx24<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461199	M	MP:0001415	increased exploration in new environment	Ddx24<em1(IMPC)Mbp>/Ddx24<+>	C57BL/6NCrl-Ddx24<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461199	F	MP:0002135	abnormal kidney morphology	Ddx24<em1(IMPC)Mbp>/Ddx24<+>	C57BL/6NCrl-Ddx24<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461199	F	MP:0001126	abnormal ovary morphology	Ddx24<em1(IMPC)Mbp>/Ddx24<+>	C57BL/6NCrl-Ddx24<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461199	F	MP:0020421	increased freezing behavior	Ddx24<em1(IMPC)Mbp>/Ddx24<+>	C57BL/6NCrl-Ddx24<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461200	M	MP:0010025	decreased total body fat amount	Ddx51<tm1a(KOMP)Wtsi>/Ddx51<+>	C57BL/6N-Ddx51<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461200	M	MP:0005179	decreased circulating cholesterol level	Ddx51<tm1a(KOMP)Wtsi>/Ddx51<+>	C57BL/6N-Ddx51<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461201	M	MP:0005573	increased pulmonary respiratory rate	Decr2<tm1b(EUCOMM)Wtsi>/Decr2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Decr2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6461201	M	MP:0005553	increased circulating creatinine level	Decr2<tm1b(EUCOMM)Wtsi>/Decr2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Decr2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6461201	M	MP:0003928	increased heart rate variability	Decr2<tm1b(EUCOMM)Wtsi>/Decr2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Decr2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6461201	M	MP:0010052	increased grip strength	Decr2<tm1b(EUCOMM)Wtsi>/Decr2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Decr2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6461202	F	MP:0003720	abnormal neural tube closure	Dennd1a<em1(IMPC)Mbp>/Dennd1a<+>	C57BL/6N-Dennd1a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461202	F	MP:0002151	abnormal neural tube morphology	Dennd1a<em1(IMPC)Mbp>/Dennd1a<+>	C57BL/6N-Dennd1a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461204	F	MP:0005560	decreased circulating glucose level	Dgkd<em1(IMPC)H>/Dgkd<+>	C57BL/6NTac-Dgkd<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461204	M	MP:0003961	decreased lean body mass	Dgkd<em1(IMPC)H>/Dgkd<+>	C57BL/6NTac-Dgkd<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461205	F	MP:0001297	microphthalmia	Dhcr7<em1(IMPC)Mbp>/Dhcr7<+>	C57BL/6N-Dhcr7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461205	M	MP:0000274	enlarged heart	Dhcr7<em1(IMPC)Mbp>/Dhcr7<+>	C57BL/6N-Dhcr7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461205	M	MP:0000691	enlarged spleen	Dhcr7<em1(IMPC)Mbp>/Dhcr7<+>	C57BL/6N-Dhcr7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461205	M	MP:0000266	abnormal heart morphology	Dhcr7<em1(IMPC)Mbp>/Dhcr7<+>	C57BL/6N-Dhcr7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461205	F	MP:0002135	abnormal kidney morphology	Dhcr7<em1(IMPC)Mbp>/Dhcr7<+>	C57BL/6N-Dhcr7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461205	F	MP:0002989	small kidney	Dhcr7<em1(IMPC)Mbp>/Dhcr7<+>	C57BL/6N-Dhcr7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461205	M	MP:0000689	abnormal spleen morphology	Dhcr7<em1(IMPC)Mbp>/Dhcr7<+>	C57BL/6N-Dhcr7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461207	M	MP:0002875	decreased erythrocyte cell number	Dhx38<em1(IMPC)J>/Dhx38<+>	C57BL/6NJ-Dhx38<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461207	M	MP:0000208	decreased hematocrit	Dhx38<em1(IMPC)J>/Dhx38<+>	C57BL/6NJ-Dhx38<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461209	F	MP:0002135	abnormal kidney morphology	Dio1<em1(IMPC)Hmgu>/Dio1<em1(IMPC)Hmgu>	C57BL/6N-Dio1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461210	F	MP:0001120	abnormal uterus morphology	Dip2c<em1(IMPC)Tcp>/Dip2c<+>	C57BL/6N-Dip2c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461210	M	MP:0000706	small thymus	Dip2c<em1(IMPC)Tcp>/Dip2c<+>	C57BL/6N-Dip2c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461210	M	MP:0011874	enlarged urinary bladder	Dip2c<em1(IMPC)Tcp>/Dip2c<+>	C57BL/6N-Dip2c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461210	M	MP:0000702	enlarged lymph nodes	Dip2c<em1(IMPC)Tcp>/Dip2c<+>	C57BL/6N-Dip2c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461210	F	MP:0000220	increased monocyte cell number	Dip2c<em1(IMPC)Tcp>/Dip2c<+>	C57BL/6N-Dip2c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461211	F	MP:0000642	enlarged adrenal glands	Dip2c<em1(IMPC)Tcp>/Dip2c<em1(IMPC)Tcp>	C57BL/6N-Dip2c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461211	M	MP:0000157	abnormal sternum morphology	Dip2c<em1(IMPC)Tcp>/Dip2c<em1(IMPC)Tcp>	C57BL/6N-Dip2c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461212	F	MP:0002574	increased vertical activity	Dipk1c<em1(IMPC)J>/Dipk1c<em1(IMPC)J>	C57BL/6NJ-Dipk1c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461213	F	MP:0002989	small kidney	Disc1<em1(IMPC)Mbp>/Disc1<em1(IMPC)Mbp>	C57BL/6N-Disc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461213	M	MP:0000274	enlarged heart	Disc1<em1(IMPC)Mbp>/Disc1<em1(IMPC)Mbp>	C57BL/6N-Disc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461213	F	MP:0001399	hyperactivity	Disc1<em1(IMPC)Mbp>/Disc1<em1(IMPC)Mbp>	C57BL/6N-Disc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461213	F	MP:0002135	abnormal kidney morphology	Disc1<em1(IMPC)Mbp>/Disc1<em1(IMPC)Mbp>	C57BL/6N-Disc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461213	M	MP:0000266	abnormal heart morphology	Disc1<em1(IMPC)Mbp>/Disc1<em1(IMPC)Mbp>	C57BL/6N-Disc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461213	M	MP:0000689	abnormal spleen morphology	Disc1<em1(IMPC)Mbp>/Disc1<em1(IMPC)Mbp>	C57BL/6N-Disc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461213	M	MP:0001304	cataract	Disc1<em1(IMPC)Mbp>/Disc1<em1(IMPC)Mbp>	C57BL/6N-Disc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461214	F	MP:0002699	abnormal vitreous body morphology	Dnaja2<em1(IMPC)Mbp>/Dnaja2<+>	C57BL/6N-Dnaja2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461216	F	MP:0001926	female infertility	Dnmt3l<em1(IMPC)Bay>/Dnmt3l<em1(IMPC)Bay>	C57BL/6N-Dnmt3l<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461216	M	MP:0001925	male infertility	Dnmt3l<em1(IMPC)Bay>/Dnmt3l<em1(IMPC)Bay>	C57BL/6N-Dnmt3l<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461217	F	MP:0005553	increased circulating creatinine level	Dnpep<tm1e(EUCOMM)Wtsi>/Dnpep<tm1e(EUCOMM)Wtsi>	C57BL/6N-Dnpep<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461217	F	MP:0002599	increased mean platelet volume	Dnpep<tm1e(EUCOMM)Wtsi>/Dnpep<tm1e(EUCOMM)Wtsi>	C57BL/6N-Dnpep<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461218	M	MP:0005505	thrombocytosis	Dnttip1<tm1b(KOMP)Wtsi>/Dnttip1<+>	C57BL/6N-Dnttip1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461219	F	MP:0000063	decreased bone mineral density	Dock2<tm1b(EUCOMM)Wtsi>/Dock2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dock2<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6461219	F	MP:0004952	increased spleen weight	Dock2<tm1b(EUCOMM)Wtsi>/Dock2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dock2<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6461220	M	MP:0005016	decreased lymphocyte cell number	Dpp4<tm1b(EUCOMM)Wtsi>/Dpp4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dpp4<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6461220	M	MP:0005292	improved glucose tolerance	Dpp4<tm1b(EUCOMM)Wtsi>/Dpp4<tm1b(EUCOMM)Wtsi>	C57BL/6N-Dpp4<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6461221	F	MP:0000266	abnormal heart morphology	Drd3<em1(IMPC)Mbp>/Drd3<em1(IMPC)Mbp>	C57BL/6N-Drd3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461221	M	MP:0000692	small spleen	Drd3<em1(IMPC)Mbp>/Drd3<em1(IMPC)Mbp>	C57BL/6N-Drd3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461221	F	MP:0002188	small heart	Drd3<em1(IMPC)Mbp>/Drd3<em1(IMPC)Mbp>	C57BL/6N-Drd3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461222	M	MP:0001711	abnormal placenta morphology	Dsp<em1(IMPC)Mbp>/Dsp<+>	C57BL/6N-Dsp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461224	F	MP:0005576	decreased pulmonary ventilation	Dusp13b<tm1b(KOMP)Wtsi>/Dusp13b<tm1b(KOMP)Wtsi>	C57BL/6N-Dusp13b<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6461226	M	MP:0002075	abnormal coat/hair pigmentation	Dync1li2<em1(IMPC)J>/Dync1li2<+>	C57BL/6NJ-Dync1li2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461226	M	MP:0000367	abnormal coat/ hair morphology	Dync1li2<em1(IMPC)J>/Dync1li2<+>	C57BL/6NJ-Dync1li2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461226	F	MP:0001399	hyperactivity	Dync1li2<em1(IMPC)J>/Dync1li2<+>	C57BL/6NJ-Dync1li2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461226	M	MP:0001529	abnormal vocalization	Dync1li2<em1(IMPC)J>/Dync1li2<+>	C57BL/6NJ-Dync1li2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461227	F	MP:0003795	abnormal bone structure	Dynlrb1<tm1a(EUCOMM)Wtsi>/Dynlrb1<+>	C57BL/6N-Dynlrb1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461229	M	MP:0002574	increased vertical activity	Dzank1<tm1b(KOMP)Wtsi>/Dzank1<tm1b(KOMP)Wtsi>	C57BL/6N-Dzank1<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6461230	M	MP:0002941	increased circulating alanine transaminase level	E130311K13Rik<em1(IMPC)J>/E130311K13Rik<em1(IMPC)J>	C57BL/6NJ-E130311K13Rik<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461230	F	MP:0001399	hyperactivity	E130311K13Rik<em1(IMPC)J>/E130311K13Rik<em1(IMPC)J>	C57BL/6NJ-E130311K13Rik<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461231	F	MP:0001402	decreased locomotor activity	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461231	M	MP:0010571	shortened ST segment	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461231	M	MP:0000266	abnormal heart morphology	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461231	M	MP:0002152	abnormal brain morphology	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461231	M	MP:0000598	abnormal liver morphology	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461231	F	MP:0002060	abnormal skin morphology	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461231	F	MP:0003068	enlarged kidney	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461231	F	MP:0002135	abnormal kidney morphology	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461231	F	MP:0001325	abnormal retina morphology	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461231	M	MP:0000274	enlarged heart	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461231	F	MP:0005293	impaired glucose tolerance	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461231	F	MP:0000689	abnormal spleen morphology	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461231	M	MP:0003900	shortened QT interval	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461231	F	MP:0000691	enlarged spleen	Ebf2<em1(IMPC)Mbp>/Ebf2<+>	C57BL/6N-Ebf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461232	F	MP:0001399	hyperactivity	Ecpas<em1(IMPC)J>/Ecpas<em1(IMPC)J>	C57BL/6NJ-Ecpas<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461232	F	MP:0004924	abnormal behavior	Ecpas<em1(IMPC)J>/Ecpas<em1(IMPC)J>	C57BL/6NJ-Ecpas<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461232	M	MP:0002075	abnormal coat/hair pigmentation	Ecpas<em1(IMPC)J>/Ecpas<em1(IMPC)J>	C57BL/6NJ-Ecpas<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461232	F	MP:0020870	decreased thigmotaxis	Ecpas<em1(IMPC)J>/Ecpas<em1(IMPC)J>	C57BL/6NJ-Ecpas<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461233	M	MP:0001304	cataract	Eef1akmt2<tm1b(EUCOMM)Wtsi>/Eef1akmt2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eef1akmt2<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6461233	M	MP:0006243	impaired pupillary reflex	Eef1akmt2<tm1b(EUCOMM)Wtsi>/Eef1akmt2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eef1akmt2<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6461236	M	MP:0010025	decreased total body fat amount	Eif2ak1<em1(IMPC)Bay>/Eif2ak1<em1(IMPC)Bay>	C57BL/6N-Eif2ak1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461236	M	MP:0004952	increased spleen weight	Eif2ak1<em1(IMPC)Bay>/Eif2ak1<em1(IMPC)Bay>	C57BL/6N-Eif2ak1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461237	M	MP:0000692	small spleen	Eif2ak2<em1(IMPC)Mbp>/Eif2ak2<em1(IMPC)Mbp>	C57BL/6N-Eif2ak2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461237	F	MP:0005553	increased circulating creatinine level	Eif2ak2<em1(IMPC)Mbp>/Eif2ak2<em1(IMPC)Mbp>	C57BL/6N-Eif2ak2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461237	F	MP:0000194	increased circulating calcium level	Eif2ak2<em1(IMPC)Mbp>/Eif2ak2<em1(IMPC)Mbp>	C57BL/6N-Eif2ak2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461237	F	MP:0002965	increased circulating serum albumin level	Eif2ak2<em1(IMPC)Mbp>/Eif2ak2<em1(IMPC)Mbp>	C57BL/6N-Eif2ak2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461237	M	MP:0000689	abnormal spleen morphology	Eif2ak2<em1(IMPC)Mbp>/Eif2ak2<em1(IMPC)Mbp>	C57BL/6N-Eif2ak2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461238	F	MP:0000691	enlarged spleen	Eif2d<em1(IMPC)Mbp>/Eif2d<em1(IMPC)Mbp>	C57BL/6N-Eif2d<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461238	F	MP:0002339	abnormal lymph node morphology	Eif2d<em1(IMPC)Mbp>/Eif2d<em1(IMPC)Mbp>	C57BL/6N-Eif2d<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461238	F	MP:0000702	enlarged lymph nodes	Eif2d<em1(IMPC)Mbp>/Eif2d<em1(IMPC)Mbp>	C57BL/6N-Eif2d<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461238	F	MP:0000689	abnormal spleen morphology	Eif2d<em1(IMPC)Mbp>/Eif2d<em1(IMPC)Mbp>	C57BL/6N-Eif2d<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461238	F	MP:0001417	decreased exploration in new environment	Eif2d<em1(IMPC)Mbp>/Eif2d<em1(IMPC)Mbp>	C57BL/6N-Eif2d<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461240	M	MP:0002079	increased circulating insulin level	Elk1<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Elk1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461241	F	MP:0010024	increased total body fat amount	Emc3<tm1b(EUCOMM)Wtsi>/Emc3<+>	C57BL/6N-Emc3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6461241	F	MP:0003961	decreased lean body mass	Emc3<tm1b(EUCOMM)Wtsi>/Emc3<+>	C57BL/6N-Emc3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6461241	M	MP:0010123	increased bone mineral content	Emc3<tm1b(EUCOMM)Wtsi>/Emc3<+>	C57BL/6N-Emc3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6461242	M	MP:0001566	increased circulating phosphate level	Enpp4<em1(IMPC)Ics>/Enpp4<em1(IMPC)Ics>	C57BL/6N-Enpp4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461242	F	MP:0000063	decreased bone mineral density	Enpp4<em1(IMPC)Ics>/Enpp4<em1(IMPC)Ics>	C57BL/6N-Enpp4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461243	F	MP:0005560	decreased circulating glucose level	Enpp5<tm1b(KOMP)Mbp>/Enpp5<tm1b(KOMP)Mbp>	C57BL/6N-Enpp5<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6461244	F	MP:0000702	enlarged lymph nodes	Epha2<em1(IMPC)Mbp>/Epha2<em1(IMPC)Mbp>	C57BL/6N-Epha2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461244	F	MP:0002339	abnormal lymph node morphology	Epha2<em1(IMPC)Mbp>/Epha2<em1(IMPC)Mbp>	C57BL/6N-Epha2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461245	F	MP:0000689	abnormal spleen morphology	Ephb1<em1(IMPC)Mbp>/Ephb1<em1(IMPC)Mbp>	C57BL/6N-Ephb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461245	F	MP:0000266	abnormal heart morphology	Ephb1<em1(IMPC)Mbp>/Ephb1<em1(IMPC)Mbp>	C57BL/6N-Ephb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461245	F	MP:0000538	abnormal urinary bladder morphology	Ephb1<em1(IMPC)Mbp>/Ephb1<em1(IMPC)Mbp>	C57BL/6N-Ephb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461245	F	MP:0000274	enlarged heart	Ephb1<em1(IMPC)Mbp>/Ephb1<em1(IMPC)Mbp>	C57BL/6N-Ephb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461245	F	MP:0000691	enlarged spleen	Ephb1<em1(IMPC)Mbp>/Ephb1<em1(IMPC)Mbp>	C57BL/6N-Ephb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461245	M	MP:0000692	small spleen	Ephb1<em1(IMPC)Mbp>/Ephb1<em1(IMPC)Mbp>	C57BL/6N-Ephb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461245	M	MP:0001415	increased exploration in new environment	Ephb1<em1(IMPC)Mbp>/Ephb1<em1(IMPC)Mbp>	C57BL/6N-Ephb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461246	M	MP:0000266	abnormal heart morphology	Eppin<em1(IMPC)Mbp>/Eppin<em1(IMPC)Mbp>	C57BL/6N-Eppin<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461246	M	MP:0001146	abnormal testis morphology	Eppin<em1(IMPC)Mbp>/Eppin<em1(IMPC)Mbp>	C57BL/6N-Eppin<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461246	M	MP:0001147	small testis	Eppin<em1(IMPC)Mbp>/Eppin<em1(IMPC)Mbp>	C57BL/6N-Eppin<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461246	F	MP:0000494	abnormal cecum morphology	Eppin<em1(IMPC)Mbp>/Eppin<em1(IMPC)Mbp>	C57BL/6N-Eppin<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461246	F	MP:0009476	enlarged cecum	Eppin<em1(IMPC)Mbp>/Eppin<em1(IMPC)Mbp>	C57BL/6N-Eppin<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461246	M	MP:0005553	increased circulating creatinine level	Eppin<em1(IMPC)Mbp>/Eppin<em1(IMPC)Mbp>	C57BL/6N-Eppin<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461246	M	MP:0002188	small heart	Eppin<em1(IMPC)Mbp>/Eppin<em1(IMPC)Mbp>	C57BL/6N-Eppin<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461247	F	MP:0005576	decreased pulmonary ventilation	Eps8l1<tm2b(KOMP)Wtsi>/Eps8l1<tm2b(KOMP)Wtsi>	C57BL/6N-Eps8l1<tm2b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6461248	F	MP:0010053	decreased grip strength	Ercc4<em1(IMPC)J>/Ercc4<+>	C57BL/6NJ-Ercc4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461249	M	MP:0002059	abnormal seminal vesicle morphology	Ergic2<em1(IMPC)Hmgu>/Ergic2<+>	C57BL/6N-Ergic2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461249	M	MP:0002833	increased heart weight	Ergic2<em1(IMPC)Hmgu>/Ergic2<+>	C57BL/6N-Ergic2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461249	M	MP:0004357	long tibia	Ergic2<em1(IMPC)Hmgu>/Ergic2<+>	C57BL/6N-Ergic2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461249	F	MP:0008810	increased circulating iron level	Ergic2<em1(IMPC)Hmgu>/Ergic2<+>	C57BL/6N-Ergic2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461252	M	MP:0000599	enlarged liver	Extl3<em1(IMPC)Mbp>/Extl3<+>	C57BL/6N-Extl3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461252	F	MP:0002060	abnormal skin morphology	Extl3<em1(IMPC)Mbp>/Extl3<+>	C57BL/6N-Extl3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461252	M	MP:0001158	abnormal prostate gland morphology	Extl3<em1(IMPC)Mbp>/Extl3<+>	C57BL/6N-Extl3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461252	M	MP:0001146	abnormal testis morphology	Extl3<em1(IMPC)Mbp>/Extl3<+>	C57BL/6N-Extl3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461252	M	MP:0001147	small testis	Extl3<em1(IMPC)Mbp>/Extl3<+>	C57BL/6N-Extl3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461252	F	MP:0001297	microphthalmia	Extl3<em1(IMPC)Mbp>/Extl3<+>	C57BL/6N-Extl3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461252	F	MP:0002989	small kidney	Extl3<em1(IMPC)Mbp>/Extl3<+>	C57BL/6N-Extl3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461252	F	MP:0002092	abnormal eye morphology	Extl3<em1(IMPC)Mbp>/Extl3<+>	C57BL/6N-Extl3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461252	M	MP:0000598	abnormal liver morphology	Extl3<em1(IMPC)Mbp>/Extl3<+>	C57BL/6N-Extl3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461256	F	MP:0001566	increased circulating phosphate level	Fam168a<em1(IMPC)J>/Fam168a<em1(IMPC)J>	C57BL/6NJ-Fam168a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461256	M	MP:0004924	abnormal behavior	Fam168a<em1(IMPC)J>/Fam168a<em1(IMPC)J>	C57BL/6NJ-Fam168a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461256	F	MP:0001325	abnormal retina morphology	Fam168a<em1(IMPC)J>/Fam168a<em1(IMPC)J>	C57BL/6NJ-Fam168a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461256	M	MP:0020870	decreased thigmotaxis	Fam168a<em1(IMPC)J>/Fam168a<em1(IMPC)J>	C57BL/6NJ-Fam168a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461257	F	MP:0002966	decreased circulating alkaline phosphatase level	Fam210b<tm1b(KOMP)Mbp>/Fam210b<tm1b(KOMP)Mbp>	C57BL/6N-Fam210b<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6461257	F	MP:0005419	decreased circulating serum albumin level	Fam210b<tm1b(KOMP)Mbp>/Fam210b<tm1b(KOMP)Mbp>	C57BL/6N-Fam210b<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6461257	M	MP:0000220	increased monocyte cell number	Fam210b<tm1b(KOMP)Mbp>/Fam210b<tm1b(KOMP)Mbp>	C57BL/6N-Fam210b<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6461258	M	MP:0002591	decreased mean corpuscular volume	Fam24b<em1(IMPC)J>/Fam24b<em1(IMPC)J>	C57BL/6NJ-Fam24b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461258	F	MP:0002075	abnormal coat/hair pigmentation	Fam24b<em1(IMPC)J>/Fam24b<em1(IMPC)J>	C57BL/6NJ-Fam24b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461258	F	MP:0001529	abnormal vocalization	Fam24b<em1(IMPC)J>/Fam24b<em1(IMPC)J>	C57BL/6NJ-Fam24b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461259	M	MP:0003068	enlarged kidney	Fam32a<em1(IMPC)Mbp>/Fam32a<+>	C57BL/6N-Fam32a<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461259	F	MP:0002092	abnormal eye morphology	Fam32a<em1(IMPC)Mbp>/Fam32a<+>	C57BL/6N-Fam32a<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461259	F	MP:0000639	abnormal adrenal gland morphology	Fam32a<em1(IMPC)Mbp>/Fam32a<+>	C57BL/6N-Fam32a<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461259	F	MP:0001293	anophthalmia	Fam32a<em1(IMPC)Mbp>/Fam32a<+>	C57BL/6N-Fam32a<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461259	M	MP:0002135	abnormal kidney morphology	Fam32a<em1(IMPC)Mbp>/Fam32a<+>	C57BL/6N-Fam32a<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461261	M	MP:0002059	abnormal seminal vesicle morphology	Fam83h<em1(IMPC)Ccpcz>/Fam83h<+>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461261	M	MP:0005084	abnormal gallbladder morphology	Fam83h<em1(IMPC)Ccpcz>/Fam83h<+>	C57BL/6N-Fam83h<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461263	M	MP:0005292	improved glucose tolerance	Fastk<tm1.1(KOMP)Vlcg>/Fastk<tm1.1(KOMP)Vlcg>	C57BL/6N-Fastk<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6461263	F	MP:0002833	increased heart weight	Fastk<tm1.1(KOMP)Vlcg>/Fastk<tm1.1(KOMP)Vlcg>	C57BL/6N-Fastk<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6461264	F	MP:0001399	hyperactivity	Fbxo30<tm1b(KOMP)Wtsi>/Fbxo30<+>	C57BL/6N-Fbxo30<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461264	F	MP:0005292	improved glucose tolerance	Fbxo30<tm1b(KOMP)Wtsi>/Fbxo30<+>	C57BL/6N-Fbxo30<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461264	M	MP:0000062	increased bone mineral density	Fbxo30<tm1b(KOMP)Wtsi>/Fbxo30<+>	C57BL/6N-Fbxo30<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461264	M	MP:0001289	persistence of hyaloid vascular system	Fbxo30<tm1b(KOMP)Wtsi>/Fbxo30<+>	C57BL/6N-Fbxo30<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461264	M	MP:0001489	decreased startle reflex	Fbxo30<tm1b(KOMP)Wtsi>/Fbxo30<+>	C57BL/6N-Fbxo30<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461264	M	MP:0010123	increased bone mineral content	Fbxo30<tm1b(KOMP)Wtsi>/Fbxo30<+>	C57BL/6N-Fbxo30<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461268	M	MP:0005343	increased circulating aspartate transaminase level	Ffar2<tm1b(EUCOMM)Hmgu>/Ffar2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ffar2<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461269	M	MP:0020421	increased freezing behavior	Fhod3<em1(IMPC)Mbp>/Fhod3<+>	C57BL/6N-Fhod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461271	F	MP:0002092	abnormal eye morphology	Fkbp11<em1(IMPC)Mbp>/Fkbp11<em1(IMPC)Mbp>	C57BL/6N-Fkbp11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461271	F	MP:0000702	enlarged lymph nodes	Fkbp11<em1(IMPC)Mbp>/Fkbp11<em1(IMPC)Mbp>	C57BL/6N-Fkbp11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461271	M	MP:0000692	small spleen	Fkbp11<em1(IMPC)Mbp>/Fkbp11<em1(IMPC)Mbp>	C57BL/6N-Fkbp11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461271	F	MP:0002339	abnormal lymph node morphology	Fkbp11<em1(IMPC)Mbp>/Fkbp11<em1(IMPC)Mbp>	C57BL/6N-Fkbp11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461271	M	MP:0000689	abnormal spleen morphology	Fkbp11<em1(IMPC)Mbp>/Fkbp11<em1(IMPC)Mbp>	C57BL/6N-Fkbp11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461271	F	MP:0002152	abnormal brain morphology	Fkbp11<em1(IMPC)Mbp>/Fkbp11<em1(IMPC)Mbp>	C57BL/6N-Fkbp11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461272	M	MP:0010097	abnormal retina blood vessel morphology	Fkbp1b<tm1b(EUCOMM)Hmgu>/Fkbp1b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fkbp1b<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6461272	M	MP:0001488	increased startle reflex	Fkbp1b<tm1b(EUCOMM)Hmgu>/Fkbp1b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Fkbp1b<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6461273	M	MP:0003917	increased kidney weight	Fkbp5<tm1b(KOMP)Wtsi>/Fkbp5<+>	C57BL/6N-Fkbp5<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6461275	F	MP:0002092	abnormal eye morphology	Foxd4<em1(IMPC)Mbp>/Foxd4<em1(IMPC)Mbp>	C57BL/6N-Foxd4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461275	F	MP:0001293	anophthalmia	Foxd4<em1(IMPC)Mbp>/Foxd4<em1(IMPC)Mbp>	C57BL/6N-Foxd4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461276	F	MP:0002968	increased circulating alkaline phosphatase level	Foxj3<tm1a(EUCOMM)Wtsi>/Foxj3<tm1a(EUCOMM)Wtsi>	C57BL/6N-Foxj3<tm1a(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6461277	M	MP:0000702	enlarged lymph nodes	Foxr1<em1(IMPC)Tcp>/Foxr1<+>	C57BL/6NCrl-Foxr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461277	M	MP:0002059	abnormal seminal vesicle morphology	Foxr1<em1(IMPC)Tcp>/Foxr1<+>	C57BL/6NCrl-Foxr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461277	M	MP:0011874	enlarged urinary bladder	Foxr1<em1(IMPC)Tcp>/Foxr1<+>	C57BL/6NCrl-Foxr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461277	F	MP:0001127	small ovary	Foxr1<em1(IMPC)Tcp>/Foxr1<+>	C57BL/6NCrl-Foxr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461277	M	MP:0000692	small spleen	Foxr1<em1(IMPC)Tcp>/Foxr1<+>	C57BL/6NCrl-Foxr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461278	M	MP:0004952	increased spleen weight	Foxred1<em1(IMPC)Bay>/Foxred1<+>	C57BL/6N-Foxred1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6461285	F	MP:0002989	small kidney	Galnt13<em1(IMPC)Mbp>/Galnt13<em1(IMPC)Mbp>	C57BL/6N-Galnt13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461285	F	MP:0002135	abnormal kidney morphology	Galnt13<em1(IMPC)Mbp>/Galnt13<em1(IMPC)Mbp>	C57BL/6N-Galnt13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461285	M	MP:0002997	enlarged seminal vesicle	Galnt13<em1(IMPC)Mbp>/Galnt13<em1(IMPC)Mbp>	C57BL/6N-Galnt13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461285	M	MP:0000692	small spleen	Galnt13<em1(IMPC)Mbp>/Galnt13<em1(IMPC)Mbp>	C57BL/6N-Galnt13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461286	M	MP:0000157	abnormal sternum morphology	Gars1<em1(IMPC)Tcp>/Gars1<+>	C57BL/6NCrl-Gars1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461286	F	MP:0002060	abnormal skin morphology	Gars1<em1(IMPC)Tcp>/Gars1<+>	C57BL/6NCrl-Gars1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461286	M	MP:0000470	abnormal stomach morphology	Gars1<em1(IMPC)Tcp>/Gars1<+>	C57BL/6NCrl-Gars1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461286	M	MP:0001552	increased circulating triglyceride level	Gars1<em1(IMPC)Tcp>/Gars1<+>	C57BL/6NCrl-Gars1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461286	M	MP:0000274	enlarged heart	Gars1<em1(IMPC)Tcp>/Gars1<+>	C57BL/6NCrl-Gars1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461286	M	MP:0000692	small spleen	Gars1<em1(IMPC)Tcp>/Gars1<+>	C57BL/6NCrl-Gars1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461286	M	MP:0002059	abnormal seminal vesicle morphology	Gars1<em1(IMPC)Tcp>/Gars1<+>	C57BL/6NCrl-Gars1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461286	M	MP:0011874	enlarged urinary bladder	Gars1<em1(IMPC)Tcp>/Gars1<+>	C57BL/6NCrl-Gars1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461286	M	MP:0002092	abnormal eye morphology	Gars1<em1(IMPC)Tcp>/Gars1<+>	C57BL/6NCrl-Gars1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461286	M	MP:0001417	decreased exploration in new environment	Gars1<em1(IMPC)Tcp>/Gars1<+>	C57BL/6NCrl-Gars1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461288	M	MP:0002968	increased circulating alkaline phosphatase level	Gbp7<em1(IMPC)J>/Gbp7<em1(IMPC)J>	C57BL/6NJ-Gbp7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461289	F	MP:0011951	increased cardiac stroke volume	Gdf11<tm2b(EUCOMM)Hmgu>/Gdf11<+>	C57BL/6N-Gdf11<tm2b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6461292	M	MP:0001925	male infertility	Gk2<em1(IMPC)J>/Gk2<em1(IMPC)J>	C57BL/6NJ-Gk2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461293	M	MP:0013279	increased fasting circulating glucose level	Glp1r<tm1b(KOMP)Mbp>/Glp1r<tm1b(KOMP)Mbp>	C57BL/6N-Glp1r<tm1b(KOMP)Mbp>/H	N	MGI:5576271
MGI:6461295	F	MP:0001399	hyperactivity	Gm5547<em1(IMPC)J>/Gm5547<em1(IMPC)J>	C57BL/6NJ-Gm5547<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461296	M	MP:0002135	abnormal kidney morphology	Sirpd<em1(IMPC)Mbp>/Sirpd<em1(IMPC)Mbp>	C57BL/6N-Sirpd<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461296	M	MP:0003068	enlarged kidney	Sirpd<em1(IMPC)Mbp>/Sirpd<em1(IMPC)Mbp>	C57BL/6N-Sirpd<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461297	F	MP:0010052	increased grip strength	Gmnc<tm1b(KOMP)Wtsi>/Gmnc<+>	C57BL/6N-Gmnc<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461297	M	MP:0005633	increased circulating sodium level	Gmnc<tm1b(KOMP)Wtsi>/Gmnc<+>	C57BL/6N-Gmnc<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461298	F	MP:0000702	enlarged lymph nodes	Gmppa<em1(IMPC)Tcp>/Gmppa<em1(IMPC)Tcp>	C57BL/6N-Gmppa<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461298	F	MP:0005565	increased blood urea nitrogen level	Gmppa<em1(IMPC)Tcp>/Gmppa<em1(IMPC)Tcp>	C57BL/6N-Gmppa<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461298	F	MP:0009454	impaired contextual conditioning behavior	Gmppa<em1(IMPC)Tcp>/Gmppa<em1(IMPC)Tcp>	C57BL/6N-Gmppa<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461298	M	MP:0001314	cornea opacity	Gmppa<em1(IMPC)Tcp>/Gmppa<em1(IMPC)Tcp>	C57BL/6N-Gmppa<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461300	F	MP:0001258	decreased body length	Gnpda2<tm1.1(KOMP)Vlcg>/Gnpda2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gnpda2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6461300	M	MP:0002590	increased mean corpuscular volume	Gnpda2<tm1.1(KOMP)Vlcg>/Gnpda2<tm1.1(KOMP)Vlcg>	C57BL/6N-Gnpda2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6461301	F	MP:0002188	small heart	Gnptab<em1(IMPC)Mbp>/Gnptab<+>	C57BL/6N-Gnptab<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461301	F	MP:0000470	abnormal stomach morphology	Gnptab<em1(IMPC)Mbp>/Gnptab<+>	C57BL/6N-Gnptab<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461301	M	MP:0002699	abnormal vitreous body morphology	Gnptab<em1(IMPC)Mbp>/Gnptab<+>	C57BL/6N-Gnptab<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461301	F	MP:0002989	small kidney	Gnptab<em1(IMPC)Mbp>/Gnptab<+>	C57BL/6N-Gnptab<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461301	M	MP:0003068	enlarged kidney	Gnptab<em1(IMPC)Mbp>/Gnptab<+>	C57BL/6N-Gnptab<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461301	M	MP:0001304	cataract	Gnptab<em1(IMPC)Mbp>/Gnptab<+>	C57BL/6N-Gnptab<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461301	F	MP:0002691	small stomach	Gnptab<em1(IMPC)Mbp>/Gnptab<+>	C57BL/6N-Gnptab<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461301	F	MP:0001120	abnormal uterus morphology	Gnptab<em1(IMPC)Mbp>/Gnptab<+>	C57BL/6N-Gnptab<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461301	F	MP:0001126	abnormal ovary morphology	Gnptab<em1(IMPC)Mbp>/Gnptab<+>	C57BL/6N-Gnptab<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461301	M	MP:0001614	abnormal blood vessel morphology	Gnptab<em1(IMPC)Mbp>/Gnptab<+>	C57BL/6N-Gnptab<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461301	F	MP:0004832	enlarged ovary	Gnptab<em1(IMPC)Mbp>/Gnptab<+>	C57BL/6N-Gnptab<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461302	M	MP:0000702	enlarged lymph nodes	Golph3<em1(IMPC)Tcp>/Golph3<+>	C57BL/6NCrl-Golph3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461303	F	MP:0002699	abnormal vitreous body morphology	Got2<em1(IMPC)Mbp>/Got2<+>	C57BL/6N-Got2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461304	F	MP:0005576	decreased pulmonary ventilation	Gpank1<tm1.1(KOMP)Vlcg>/Gpank1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpank1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461304	M	MP:0005575	increased pulmonary ventilation	Gpank1<tm1.1(KOMP)Vlcg>/Gpank1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpank1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461304	M	MP:0005585	increased tidal volume	Gpank1<tm1.1(KOMP)Vlcg>/Gpank1<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpank1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461305	F	MP:0000691	enlarged spleen	Gpatch3<em1(IMPC)Mbp>/Gpatch3<em1(IMPC)Mbp>	C57BL/6N-Gpatch3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461305	M	MP:0000692	small spleen	Gpatch3<em1(IMPC)Mbp>/Gpatch3<em1(IMPC)Mbp>	C57BL/6N-Gpatch3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461305	F	MP:0002092	abnormal eye morphology	Gpatch3<em1(IMPC)Mbp>/Gpatch3<em1(IMPC)Mbp>	C57BL/6N-Gpatch3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461305	F	MP:0009084	blind uterus	Gpatch3<em1(IMPC)Mbp>/Gpatch3<em1(IMPC)Mbp>	C57BL/6N-Gpatch3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461305	F	MP:0001297	microphthalmia	Gpatch3<em1(IMPC)Mbp>/Gpatch3<em1(IMPC)Mbp>	C57BL/6N-Gpatch3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461305	F	MP:0000689	abnormal spleen morphology	Gpatch3<em1(IMPC)Mbp>/Gpatch3<em1(IMPC)Mbp>	C57BL/6N-Gpatch3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461306	F	MP:0010053	decreased grip strength	Gpc4<tm2b(EUCOMM)Wtsi>/Gpc4<tm2b(EUCOMM)Wtsi>	C57BL/6N-Gpc4<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6461306	F	MP:0000443	abnormal snout morphology	Gpc4<tm2b(EUCOMM)Wtsi>/Gpc4<tm2b(EUCOMM)Wtsi>	C57BL/6N-Gpc4<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6461306	F	MP:0005278	abnormal cholesterol homeostasis	Gpc4<tm2b(EUCOMM)Wtsi>/Gpc4<tm2b(EUCOMM)Wtsi>	C57BL/6N-Gpc4<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6461306	F	MP:0005344	increased circulating bilirubin level	Gpc4<tm2b(EUCOMM)Wtsi>/Gpc4<tm2b(EUCOMM)Wtsi>	C57BL/6N-Gpc4<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6461307	M	MP:0000702	enlarged lymph nodes	Gpcpd1<em1(IMPC)Tcp>/Gpcpd1<+>	C57BL/6N-Gpcpd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461307	F	MP:0009142	decreased prepulse inhibition	Gpcpd1<em1(IMPC)Tcp>/Gpcpd1<+>	C57BL/6N-Gpcpd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461307	M	MP:0005419	decreased circulating serum albumin level	Gpcpd1<em1(IMPC)Tcp>/Gpcpd1<+>	C57BL/6N-Gpcpd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461307	F	MP:0000157	abnormal sternum morphology	Gpcpd1<em1(IMPC)Tcp>/Gpcpd1<+>	C57BL/6N-Gpcpd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461309	M	MP:0001146	abnormal testis morphology	Gpr160<em1(IMPC)Mbp>/Gpr160<em1(IMPC)Mbp>	C57BL/6N-Gpr160<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461309	M	MP:0001147	small testis	Gpr160<em1(IMPC)Mbp>/Gpr160<em1(IMPC)Mbp>	C57BL/6N-Gpr160<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461309	M	MP:0020421	increased freezing behavior	Gpr160<em1(IMPC)Mbp>/Gpr160<em1(IMPC)Mbp>	C57BL/6N-Gpr160<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461312	M	MP:0005293	impaired glucose tolerance	Gramd2b<em1(IMPC)J>/Gramd2b<em1(IMPC)J>	C57BL/6NJ-Gramd2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461312	F	MP:0001513	limb grasping	Gramd2b<em1(IMPC)J>/Gramd2b<em1(IMPC)J>	C57BL/6NJ-Gramd2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461312	F	MP:0001303	abnormal lens morphology	Gramd2b<em1(IMPC)J>/Gramd2b<em1(IMPC)J>	C57BL/6NJ-Gramd2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461312	M	MP:0000367	abnormal coat/ hair morphology	Gramd2b<em1(IMPC)J>/Gramd2b<em1(IMPC)J>	C57BL/6NJ-Gramd2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461312	F	MP:0001523	impaired righting response	Gramd2b<em1(IMPC)J>/Gramd2b<em1(IMPC)J>	C57BL/6NJ-Gramd2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461313	F	MP:0001258	decreased body length	Grik3<em1(IMPC)Mbp>/Grik3<em1(IMPC)Mbp>	C57BL/6N-Grik3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461313	F	MP:0002989	small kidney	Grik3<em1(IMPC)Mbp>/Grik3<em1(IMPC)Mbp>	C57BL/6N-Grik3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461313	F	MP:0002135	abnormal kidney morphology	Grik3<em1(IMPC)Mbp>/Grik3<em1(IMPC)Mbp>	C57BL/6N-Grik3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461313	F	MP:0009084	blind uterus	Grik3<em1(IMPC)Mbp>/Grik3<em1(IMPC)Mbp>	C57BL/6N-Grik3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461313	F	MP:0013279	increased fasting circulating glucose level	Grik3<em1(IMPC)Mbp>/Grik3<em1(IMPC)Mbp>	C57BL/6N-Grik3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461313	F	MP:0004924	abnormal behavior	Grik3<em1(IMPC)Mbp>/Grik3<em1(IMPC)Mbp>	C57BL/6N-Grik3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461313	M	MP:0000689	abnormal spleen morphology	Grik3<em1(IMPC)Mbp>/Grik3<em1(IMPC)Mbp>	C57BL/6N-Grik3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461313	M	MP:0002060	abnormal skin morphology	Grik3<em1(IMPC)Mbp>/Grik3<em1(IMPC)Mbp>	C57BL/6N-Grik3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461313	F	MP:0020870	decreased thigmotaxis	Grik3<em1(IMPC)Mbp>/Grik3<em1(IMPC)Mbp>	C57BL/6N-Grik3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461314	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Gsdme<tm1b(KOMP)Wtsi>/Gsdme<tm1b(KOMP)Wtsi>	C57BL/6N-Gsdme<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461314	F	MP:0010087	increased circulating fructosamine level	Gsdme<tm1b(KOMP)Wtsi>/Gsdme<tm1b(KOMP)Wtsi>	C57BL/6N-Gsdme<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461315	M	MP:0006243	impaired pupillary reflex	Gspt2<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Gspt2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461316	M	MP:0002599	increased mean platelet volume	Gtf2e2<tm1b(EUCOMM)Wtsi>/Gtf2e2<+>	C57BL/6N-Gtf2e2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6461318	F	MP:0002098	abnormal vibrissa morphology	Gtpbp10<tm1b(KOMP)Mbp>/Gtpbp10<tm1b(KOMP)Mbp>	C57BL/6N-Gtpbp10<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6461318	M	MP:0002626	increased heart rate	Gtpbp10<tm1b(KOMP)Mbp>/Gtpbp10<tm1b(KOMP)Mbp>	C57BL/6N-Gtpbp10<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6461318	F	MP:0005553	increased circulating creatinine level	Gtpbp10<tm1b(KOMP)Mbp>/Gtpbp10<tm1b(KOMP)Mbp>	C57BL/6N-Gtpbp10<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6461318	F	MP:0013278	decreased fasting circulating glucose level	Gtpbp10<tm1b(KOMP)Mbp>/Gtpbp10<tm1b(KOMP)Mbp>	C57BL/6N-Gtpbp10<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6461318	M	MP:0010123	increased bone mineral content	Gtpbp10<tm1b(KOMP)Mbp>/Gtpbp10<tm1b(KOMP)Mbp>	C57BL/6N-Gtpbp10<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6461319	F	MP:0011110	preweaning lethality, incomplete penetrance	Gtpbp6<em1(IMPC)Bay>/Gtpbp6<em1(IMPC)Bay>	C57BL/6N-Gtpbp6<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461320	M	MP:0010025	decreased total body fat amount	Gulp1<em1(IMPC)J>/Gulp1<em1(IMPC)J>	C57BL/6NJ-Gulp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461321	M	MP:0003960	increased lean body mass	Gxylt2<em1(IMPC)Bay>/Gxylt2<em1(IMPC)Bay>	C57BL/6N-Gxylt2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461321	F	MP:0010097	abnormal retina blood vessel morphology	Gxylt2<em1(IMPC)Bay>/Gxylt2<em1(IMPC)Bay>	C57BL/6N-Gxylt2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461321	M	MP:0010025	decreased total body fat amount	Gxylt2<em1(IMPC)Bay>/Gxylt2<em1(IMPC)Bay>	C57BL/6N-Gxylt2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461323	F	MP:0009709	hydrometra	H1f0<em1(IMPC)Mbp>/H1f0<em1(IMPC)Mbp>	C57BL/6N-H1f0<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461323	F	MP:0001120	abnormal uterus morphology	H1f0<em1(IMPC)Mbp>/H1f0<em1(IMPC)Mbp>	C57BL/6N-H1f0<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461323	M	MP:0002135	abnormal kidney morphology	H1f0<em1(IMPC)Mbp>/H1f0<em1(IMPC)Mbp>	C57BL/6N-H1f0<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461323	M	MP:0003068	enlarged kidney	H1f0<em1(IMPC)Mbp>/H1f0<em1(IMPC)Mbp>	C57BL/6N-H1f0<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461325	F	MP:0005562	decreased mean corpuscular hemoglobin	H4c16<em1(IMPC)Mbp>/H4c16<em1(IMPC)Mbp>	C57BL/6N-H4c16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461325	M	MP:0003068	enlarged kidney	H4c16<em1(IMPC)Mbp>/H4c16<em1(IMPC)Mbp>	C57BL/6N-H4c16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461325	M	MP:0002135	abnormal kidney morphology	H4c16<em1(IMPC)Mbp>/H4c16<em1(IMPC)Mbp>	C57BL/6N-H4c16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461327	M	MP:0005565	increased blood urea nitrogen level	Hap1<tm1b(KOMP)Wtsi>/Hap1<+>	C57BL/6N-Hap1<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461328	F	MP:0010053	decreased grip strength	Hars2<em1(IMPC)J>/Hars2<+>	C57BL/6NJ-Hars2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461331	M	MP:0002135	abnormal kidney morphology	Hibch<em1(IMPC)Tcp>/Hibch<+>	C57BL/6N-Hibch<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461332	M	MP:0000219	increased neutrophil cell number	Hif1an<em1(IMPC)Mbp>/Hif1an<em1(IMPC)Mbp>	C57BL/6N-Hif1an<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461332	F	MP:0000598	abnormal liver morphology	Hif1an<em1(IMPC)Mbp>/Hif1an<em1(IMPC)Mbp>	C57BL/6N-Hif1an<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461332	F	MP:0003795	abnormal bone structure	Hif1an<em1(IMPC)Mbp>/Hif1an<em1(IMPC)Mbp>	C57BL/6N-Hif1an<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461332	M	MP:0010392	prolonged QRS complex duration	Hif1an<em1(IMPC)Mbp>/Hif1an<em1(IMPC)Mbp>	C57BL/6N-Hif1an<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461332	M	MP:0000691	enlarged spleen	Hif1an<em1(IMPC)Mbp>/Hif1an<em1(IMPC)Mbp>	C57BL/6N-Hif1an<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461332	M	MP:0000689	abnormal spleen morphology	Hif1an<em1(IMPC)Mbp>/Hif1an<em1(IMPC)Mbp>	C57BL/6N-Hif1an<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461332	M	MP:0002092	abnormal eye morphology	Hif1an<em1(IMPC)Mbp>/Hif1an<em1(IMPC)Mbp>	C57BL/6N-Hif1an<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461332	F	MP:0009142	decreased prepulse inhibition	Hif1an<em1(IMPC)Mbp>/Hif1an<em1(IMPC)Mbp>	C57BL/6N-Hif1an<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461332	F	MP:0000601	small liver	Hif1an<em1(IMPC)Mbp>/Hif1an<em1(IMPC)Mbp>	C57BL/6N-Hif1an<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461332	F	MP:0001417	decreased exploration in new environment	Hif1an<em1(IMPC)Mbp>/Hif1an<em1(IMPC)Mbp>	C57BL/6N-Hif1an<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461333	M	MP:0002060	abnormal skin morphology	Hk3<em1(IMPC)Tcp>/Hk3<em1(IMPC)Tcp>	C57BL/6N-Hk3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461333	M	MP:0002768	small adrenal glands	Hk3<em1(IMPC)Tcp>/Hk3<em1(IMPC)Tcp>	C57BL/6N-Hk3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461333	M	MP:0000702	enlarged lymph nodes	Hk3<em1(IMPC)Tcp>/Hk3<em1(IMPC)Tcp>	C57BL/6N-Hk3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461334	F	MP:0001399	hyperactivity	Hmg20a<em1(IMPC)J>/Hmg20a<+>	C57BL/6NJ-Hmg20a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461335	M	MP:0003961	decreased lean body mass	Hmgn1<em1(IMPC)Ics>/Hmgn1<em1(IMPC)Ics>	C57BL/6N-Hmgn1<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461335	F	MP:0011940	decreased food intake	Hmgn1<em1(IMPC)Ics>/Hmgn1<em1(IMPC)Ics>	C57BL/6N-Hmgn1<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461335	M	MP:0005554	decreased circulating creatinine level	Hmgn1<em1(IMPC)Ics>/Hmgn1<em1(IMPC)Ics>	C57BL/6N-Hmgn1<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461335	M	MP:0010024	increased total body fat amount	Hmgn1<em1(IMPC)Ics>/Hmgn1<em1(IMPC)Ics>	C57BL/6N-Hmgn1<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461337	F	MP:0001529	abnormal vocalization	Hnrnph2<em1(IMPC)J>/Hnrnph2<em1(IMPC)J>	C57BL/6NJ-Hnrnph2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461337	F	MP:0000428	abnormal craniofacial morphology	Hnrnph2<em1(IMPC)J>/Hnrnph2<em1(IMPC)J>	C57BL/6NJ-Hnrnph2<em1(IMPC)J>/Mmjax	N	37463454
MGI:6461337	F	MP:0002075	abnormal coat/hair pigmentation	Hnrnph2<em1(IMPC)J>/Hnrnph2<em1(IMPC)J>	C57BL/6NJ-Hnrnph2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461337	F	MP:0000367	abnormal coat/ hair morphology	Hnrnph2<em1(IMPC)J>/Hnrnph2<em1(IMPC)J>	C57BL/6NJ-Hnrnph2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461338	M	MP:0005419	decreased circulating serum albumin level	Hrnr<em1(IMPC)Wtsi>/Hrnr<em1(IMPC)Wtsi>	C57BL/6N-Hrnr<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6461339	M	MP:0000274	enlarged heart	Hs3st3b1<em2(IMPC)Mbp>/Hs3st3b1<em2(IMPC)Mbp>	C57BL/6N-Hs3st3b1<em2(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461339	M	MP:0000266	abnormal heart morphology	Hs3st3b1<em2(IMPC)Mbp>/Hs3st3b1<em2(IMPC)Mbp>	C57BL/6N-Hs3st3b1<em2(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461339	M	MP:0000689	abnormal spleen morphology	Hs3st3b1<em2(IMPC)Mbp>/Hs3st3b1<em2(IMPC)Mbp>	C57BL/6N-Hs3st3b1<em2(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461339	F	MP:0020421	increased freezing behavior	Hs3st3b1<em2(IMPC)Mbp>/Hs3st3b1<em2(IMPC)Mbp>	C57BL/6N-Hs3st3b1<em2(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461339	M	MP:0000598	abnormal liver morphology	Hs3st3b1<em2(IMPC)Mbp>/Hs3st3b1<em2(IMPC)Mbp>	C57BL/6N-Hs3st3b1<em2(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461339	M	MP:0000691	enlarged spleen	Hs3st3b1<em2(IMPC)Mbp>/Hs3st3b1<em2(IMPC)Mbp>	C57BL/6N-Hs3st3b1<em2(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461339	F	MP:0020420	abnormal freezing behavior	Hs3st3b1<em2(IMPC)Mbp>/Hs3st3b1<em2(IMPC)Mbp>	C57BL/6N-Hs3st3b1<em2(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461339	M	MP:0002060	abnormal skin morphology	Hs3st3b1<em2(IMPC)Mbp>/Hs3st3b1<em2(IMPC)Mbp>	C57BL/6N-Hs3st3b1<em2(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461339	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Hs3st3b1<em2(IMPC)Mbp>/Hs3st3b1<em2(IMPC)Mbp>	C57BL/6N-Hs3st3b1<em2(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461340	F	MP:0002989	small kidney	Hs3st5<em1(IMPC)Mbp>/Hs3st5<em1(IMPC)Mbp>	C57BL/6N-Hs3st5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461340	F	MP:0001399	hyperactivity	Hs3st5<em1(IMPC)Mbp>/Hs3st5<em1(IMPC)Mbp>	C57BL/6N-Hs3st5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461340	F	MP:0002092	abnormal eye morphology	Hs3st5<em1(IMPC)Mbp>/Hs3st5<em1(IMPC)Mbp>	C57BL/6N-Hs3st5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461340	F	MP:0002135	abnormal kidney morphology	Hs3st5<em1(IMPC)Mbp>/Hs3st5<em1(IMPC)Mbp>	C57BL/6N-Hs3st5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461341	M	MP:0000274	enlarged heart	Hsd17b4<em1(IMPC)Tcp>/Hsd17b4<+>	C57BL/6NCrl-Hsd17b4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461341	M	MP:0011874	enlarged urinary bladder	Hsd17b4<em1(IMPC)Tcp>/Hsd17b4<+>	C57BL/6NCrl-Hsd17b4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461341	M	MP:0005632	decreased circulating aspartate transaminase level	Hsd17b4<em1(IMPC)Tcp>/Hsd17b4<+>	C57BL/6NCrl-Hsd17b4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461341	M	MP:0002059	abnormal seminal vesicle morphology	Hsd17b4<em1(IMPC)Tcp>/Hsd17b4<+>	C57BL/6NCrl-Hsd17b4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461341	F	MP:0002637	small uterus	Hsd17b4<em1(IMPC)Tcp>/Hsd17b4<+>	C57BL/6NCrl-Hsd17b4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461341	M	MP:0010052	increased grip strength	Hsd17b4<em1(IMPC)Tcp>/Hsd17b4<+>	C57BL/6NCrl-Hsd17b4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461342	M	MP:0001925	male infertility	Hsdl2<em1(IMPC)Bay>/Hsdl2<em1(IMPC)Bay>	C57BL/6N-Hsdl2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461344	F	MP:0002941	increased circulating alanine transaminase level	Ier3ip1<em1(IMPC)J>/Ier3ip1<+>	C57BL/6NJ-Ier3ip1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461344	F	MP:0001402	decreased locomotor activity	Ier3ip1<em1(IMPC)J>/Ier3ip1<+>	C57BL/6NJ-Ier3ip1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461345	F	MP:0009709	hydrometra	Ifi208<em1(IMPC)Mbp>/Ifi208<em1(IMPC)Mbp>	C57BL/6N-Ifi208<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461345	M	MP:0000689	abnormal spleen morphology	Ifi208<em1(IMPC)Mbp>/Ifi208<em1(IMPC)Mbp>	C57BL/6N-Ifi208<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461345	M	MP:0000692	small spleen	Ifi208<em1(IMPC)Mbp>/Ifi208<em1(IMPC)Mbp>	C57BL/6N-Ifi208<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461345	M	MP:0002092	abnormal eye morphology	Ifi208<em1(IMPC)Mbp>/Ifi208<em1(IMPC)Mbp>	C57BL/6N-Ifi208<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461345	F	MP:0001120	abnormal uterus morphology	Ifi208<em1(IMPC)Mbp>/Ifi208<em1(IMPC)Mbp>	C57BL/6N-Ifi208<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461349	M	MP:0002092	abnormal eye morphology	Il21r<em1(IMPC)Mbp>/Il21r<em1(IMPC)Mbp>	C57BL/6N-Il21r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461349	M	MP:0002135	abnormal kidney morphology	Il21r<em1(IMPC)Mbp>/Il21r<em1(IMPC)Mbp>	C57BL/6N-Il21r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461349	M	MP:0001415	increased exploration in new environment	Il21r<em1(IMPC)Mbp>/Il21r<em1(IMPC)Mbp>	C57BL/6N-Il21r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461349	M	MP:0003068	enlarged kidney	Il21r<em1(IMPC)Mbp>/Il21r<em1(IMPC)Mbp>	C57BL/6N-Il21r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461350	F	MP:0000266	abnormal heart morphology	Il6<tm1.1(KOMP)Vlcg>/Il6<tm1.1(KOMP)Vlcg>	C57BL/6N-Il6<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461350	F	MP:0000274	enlarged heart	Il6<tm1.1(KOMP)Vlcg>/Il6<tm1.1(KOMP)Vlcg>	C57BL/6N-Il6<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461352	M	MP:0000219	increased neutrophil cell number	Inpp5k<em1(IMPC)H>/Inpp5k<+>	C57BL/6NTac-Inpp5k<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461355	F	MP:0002135	abnormal kidney morphology	Irf3<em1(IMPC)Mbp>/Irf3<em1(IMPC)Mbp>	C57BL/6N-Irf3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461355	F	MP:0002989	small kidney	Irf3<em1(IMPC)Mbp>/Irf3<em1(IMPC)Mbp>	C57BL/6N-Irf3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461355	F	MP:0000702	enlarged lymph nodes	Irf3<em1(IMPC)Mbp>/Irf3<em1(IMPC)Mbp>	C57BL/6N-Irf3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461355	M	MP:0000266	abnormal heart morphology	Irf3<em1(IMPC)Mbp>/Irf3<em1(IMPC)Mbp>	C57BL/6N-Irf3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461355	M	MP:0001566	increased circulating phosphate level	Irf3<em1(IMPC)Mbp>/Irf3<em1(IMPC)Mbp>	C57BL/6N-Irf3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461355	M	MP:0002188	small heart	Irf3<em1(IMPC)Mbp>/Irf3<em1(IMPC)Mbp>	C57BL/6N-Irf3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461358	F	MP:0001399	hyperactivity	Iws1<em1(IMPC)J>/Iws1<+>	C57BL/6NJ-Iws1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461359	F	MP:0011960	abnormal eye anterior chamber depth	Kank1<em1(IMPC)Bay>/Kank1<em1(IMPC)Bay>	C57BL/6N-Kank1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461360	F	MP:0003961	decreased lean body mass	Kash5<em1(IMPC)J>/Kash5<em1(IMPC)J>	C57BL/6NJ-Kash5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461360	F	MP:0000063	decreased bone mineral density	Kash5<em1(IMPC)J>/Kash5<em1(IMPC)J>	C57BL/6NJ-Kash5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461360	M	MP:0001925	male infertility	Kash5<em1(IMPC)J>/Kash5<em1(IMPC)J>	C57BL/6NJ-Kash5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461360	F	MP:0001402	decreased locomotor activity	Kash5<em1(IMPC)J>/Kash5<em1(IMPC)J>	C57BL/6NJ-Kash5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461360	F	MP:0010124	decreased bone mineral content	Kash5<em1(IMPC)J>/Kash5<em1(IMPC)J>	C57BL/6NJ-Kash5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461360	F	MP:0000218	increased leukocyte cell number	Kash5<em1(IMPC)J>/Kash5<em1(IMPC)J>	C57BL/6NJ-Kash5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461360	F	MP:0001926	female infertility	Kash5<em1(IMPC)J>/Kash5<em1(IMPC)J>	C57BL/6NJ-Kash5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461360	F	MP:0003795	abnormal bone structure	Kash5<em1(IMPC)J>/Kash5<em1(IMPC)J>	C57BL/6NJ-Kash5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461360	F	MP:0010024	increased total body fat amount	Kash5<em1(IMPC)J>/Kash5<em1(IMPC)J>	C57BL/6NJ-Kash5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461361	F	MP:0009084	blind uterus	Kat8<em1(IMPC)Mbp>/Kat8<+>	C57BL/6N-Kat8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461361	M	MP:0000702	enlarged lymph nodes	Kat8<em1(IMPC)Mbp>/Kat8<+>	C57BL/6N-Kat8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461361	M	MP:0002135	abnormal kidney morphology	Kat8<em1(IMPC)Mbp>/Kat8<+>	C57BL/6N-Kat8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461361	M	MP:0001402	decreased locomotor activity	Kat8<em1(IMPC)Mbp>/Kat8<+>	C57BL/6N-Kat8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461361	M	MP:0020870	decreased thigmotaxis	Kat8<em1(IMPC)Mbp>/Kat8<+>	C57BL/6N-Kat8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461361	F	MP:0002188	small heart	Kat8<em1(IMPC)Mbp>/Kat8<+>	C57BL/6N-Kat8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461361	M	MP:0005178	increased circulating cholesterol level	Kat8<em1(IMPC)Mbp>/Kat8<+>	C57BL/6N-Kat8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461361	M	MP:0004924	abnormal behavior	Kat8<em1(IMPC)Mbp>/Kat8<+>	C57BL/6N-Kat8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461361	F	MP:0002699	abnormal vitreous body morphology	Kat8<em1(IMPC)Mbp>/Kat8<+>	C57BL/6N-Kat8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461361	M	MP:0002339	abnormal lymph node morphology	Kat8<em1(IMPC)Mbp>/Kat8<+>	C57BL/6N-Kat8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461361	M	MP:0000598	abnormal liver morphology	Kat8<em1(IMPC)Mbp>/Kat8<+>	C57BL/6N-Kat8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461362	F	MP:0000063	decreased bone mineral density	Kbtbd8<em1(IMPC)Tcp>/Kbtbd8<em1(IMPC)Tcp>	C57BL/6N-Kbtbd8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461362	F	MP:0010124	decreased bone mineral content	Kbtbd8<em1(IMPC)Tcp>/Kbtbd8<em1(IMPC)Tcp>	C57BL/6N-Kbtbd8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461362	F	MP:0010024	increased total body fat amount	Kbtbd8<em1(IMPC)Tcp>/Kbtbd8<em1(IMPC)Tcp>	C57BL/6N-Kbtbd8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461362	M	MP:0002941	increased circulating alanine transaminase level	Kbtbd8<em1(IMPC)Tcp>/Kbtbd8<em1(IMPC)Tcp>	C57BL/6N-Kbtbd8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461362	M	MP:0005562	decreased mean corpuscular hemoglobin	Kbtbd8<em1(IMPC)Tcp>/Kbtbd8<em1(IMPC)Tcp>	C57BL/6N-Kbtbd8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461362	F	MP:0002764	short tibia	Kbtbd8<em1(IMPC)Tcp>/Kbtbd8<em1(IMPC)Tcp>	C57BL/6N-Kbtbd8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461362	F	MP:0003961	decreased lean body mass	Kbtbd8<em1(IMPC)Tcp>/Kbtbd8<em1(IMPC)Tcp>	C57BL/6N-Kbtbd8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461363	F	MP:0002574	increased vertical activity	Kcna6<em1(IMPC)J>/Kcna6<em1(IMPC)J>	C57BL/6NJ-Kcna6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461363	F	MP:0001415	increased exploration in new environment	Kcna6<em1(IMPC)J>/Kcna6<em1(IMPC)J>	C57BL/6NJ-Kcna6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461364	F	MP:0005568	increased circulating total protein level	Kcnh6<tm1.1(KOMP)Vlcg>/Kcnh6<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnh6<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6461364	M	MP:0003068	enlarged kidney	Kcnh6<tm1.1(KOMP)Vlcg>/Kcnh6<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnh6<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6461364	M	MP:0002060	abnormal skin morphology	Kcnh6<tm1.1(KOMP)Vlcg>/Kcnh6<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnh6<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6461364	F	MP:0000194	increased circulating calcium level	Kcnh6<tm1.1(KOMP)Vlcg>/Kcnh6<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnh6<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6461364	M	MP:0002135	abnormal kidney morphology	Kcnh6<tm1.1(KOMP)Vlcg>/Kcnh6<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnh6<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6461364	F	MP:0002965	increased circulating serum albumin level	Kcnh6<tm1.1(KOMP)Vlcg>/Kcnh6<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnh6<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6461365	F	MP:0002757	decreased vertical activity	Kcnh7<em1(IMPC)Hmgu>/Kcnh7<em1(IMPC)Hmgu>	C57BL/6N-Kcnh7<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461367	M	MP:0005576	decreased pulmonary ventilation	Kcnj3<tm1.1(KOMP)Vlcg>/Kcnj3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnj3<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461367	M	MP:0005575	increased pulmonary ventilation	Kcnj3<tm1.1(KOMP)Vlcg>/Kcnj3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnj3<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461367	M	MP:0005574	decreased pulmonary respiratory rate	Kcnj3<tm1.1(KOMP)Vlcg>/Kcnj3<tm1.1(KOMP)Vlcg>	C57BL/6N-Kcnj3<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461368	M	MP:0002102	abnormal ear morphology	Kcnma1<em1(IMPC)H>/Kcnma1<em1(IMPC)H>	C57BL/6N-Kcnma1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461368	F	MP:0004953	decreased spleen weight	Kcnma1<em1(IMPC)H>/Kcnma1<em1(IMPC)H>	C57BL/6N-Kcnma1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461368	F	MP:0002968	increased circulating alkaline phosphatase level	Kcnma1<em1(IMPC)H>/Kcnma1<em1(IMPC)H>	C57BL/6N-Kcnma1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461368	F	MP:0001392	abnormal locomotor behavior	Kcnma1<em1(IMPC)H>/Kcnma1<em1(IMPC)H>	C57BL/6N-Kcnma1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461369	F	MP:0000443	abnormal snout morphology	Kcnq3<em1(IMPC)H>/Kcnq3<em1(IMPC)H>	C57BL/6N-Kcnq3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461369	F	MP:0001415	increased exploration in new environment	Kcnq3<em1(IMPC)H>/Kcnq3<em1(IMPC)H>	C57BL/6N-Kcnq3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461370	M	MP:0002989	small kidney	Kcnt1<em1(IMPC)Mbp>/Kcnt1<em1(IMPC)Mbp>	C57BL/6N-Kcnt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461370	M	MP:0000689	abnormal spleen morphology	Kcnt1<em1(IMPC)Mbp>/Kcnt1<em1(IMPC)Mbp>	C57BL/6N-Kcnt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461370	M	MP:0001364	decreased anxiety-related response	Kcnt1<em1(IMPC)Mbp>/Kcnt1<em1(IMPC)Mbp>	C57BL/6N-Kcnt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461370	F	MP:0002092	abnormal eye morphology	Kcnt1<em1(IMPC)Mbp>/Kcnt1<em1(IMPC)Mbp>	C57BL/6N-Kcnt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461370	M	MP:0001402	decreased locomotor activity	Kcnt1<em1(IMPC)Mbp>/Kcnt1<em1(IMPC)Mbp>	C57BL/6N-Kcnt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461370	M	MP:0001417	decreased exploration in new environment	Kcnt1<em1(IMPC)Mbp>/Kcnt1<em1(IMPC)Mbp>	C57BL/6N-Kcnt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461370	M	MP:0004924	abnormal behavior	Kcnt1<em1(IMPC)Mbp>/Kcnt1<em1(IMPC)Mbp>	C57BL/6N-Kcnt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461370	F	MP:0001293	anophthalmia	Kcnt1<em1(IMPC)Mbp>/Kcnt1<em1(IMPC)Mbp>	C57BL/6N-Kcnt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461370	M	MP:0020870	decreased thigmotaxis	Kcnt1<em1(IMPC)Mbp>/Kcnt1<em1(IMPC)Mbp>	C57BL/6N-Kcnt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461370	M	MP:0002135	abnormal kidney morphology	Kcnt1<em1(IMPC)Mbp>/Kcnt1<em1(IMPC)Mbp>	C57BL/6N-Kcnt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461370	M	MP:0000692	small spleen	Kcnt1<em1(IMPC)Mbp>/Kcnt1<em1(IMPC)Mbp>	C57BL/6N-Kcnt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461371	M	MP:0009453	enhanced contextual conditioning behavior	Kcnt2<em1(IMPC)Mbp>/Kcnt2<em1(IMPC)Mbp>	C57BL/6N-Kcnt2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461372	F	MP:0005553	increased circulating creatinine level	Kctd15<tm1b(EUCOMM)Wtsi>/Kctd15<+>	C57BL/6N-Kctd15<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6461374	M	MP:0005178	increased circulating cholesterol level	Kctd19<em1(IMPC)J>/Kctd19<em1(IMPC)J>	C57BL/6NJ-Kctd19<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461374	M	MP:0011953	prolonged PQ interval	Kctd19<em1(IMPC)J>/Kctd19<em1(IMPC)J>	C57BL/6NJ-Kctd19<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461374	M	MP:0002075	abnormal coat/hair pigmentation	Kctd19<em1(IMPC)J>/Kctd19<em1(IMPC)J>	C57BL/6NJ-Kctd19<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461374	M	MP:0001925	male infertility	Kctd19<em1(IMPC)J>/Kctd19<em1(IMPC)J>	C57BL/6NJ-Kctd19<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461375	M	MP:0013279	increased fasting circulating glucose level	Kctd7<em2(IMPC)Bay>/Kctd7<em2(IMPC)Bay>	C57BL/6N-Kctd7<em2(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461375	M	MP:0010025	decreased total body fat amount	Kctd7<em2(IMPC)Bay>/Kctd7<em2(IMPC)Bay>	C57BL/6N-Kctd7<em2(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461376	F	MP:0009142	decreased prepulse inhibition	Kdm3b<em1(IMPC)Tcp>/Kdm3b<+>	C57BL/6NCrl-Kdm3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461376	M	MP:0001417	decreased exploration in new environment	Kdm3b<em1(IMPC)Tcp>/Kdm3b<+>	C57BL/6NCrl-Kdm3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461376	M	MP:0001258	decreased body length	Kdm3b<em1(IMPC)Tcp>/Kdm3b<+>	C57BL/6NCrl-Kdm3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461376	M	MP:0000157	abnormal sternum morphology	Kdm3b<em1(IMPC)Tcp>/Kdm3b<+>	C57BL/6NCrl-Kdm3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461376	M	MP:0002060	abnormal skin morphology	Kdm3b<em1(IMPC)Tcp>/Kdm3b<+>	C57BL/6NCrl-Kdm3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461376	M	MP:0002590	increased mean corpuscular volume	Kdm3b<em1(IMPC)Tcp>/Kdm3b<+>	C57BL/6NCrl-Kdm3b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461378	M	MP:0002060	abnormal skin morphology	Kif9<em1(IMPC)Mbp>/Kif9<em1(IMPC)Mbp>	C57BL/6N-Kif9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461378	F	MP:0000598	abnormal liver morphology	Kif9<em1(IMPC)Mbp>/Kif9<em1(IMPC)Mbp>	C57BL/6N-Kif9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461378	M	MP:0001925	male infertility	Kif9<em1(IMPC)Mbp>/Kif9<em1(IMPC)Mbp>	C57BL/6N-Kif9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461378	F	MP:0009084	blind uterus	Kif9<em1(IMPC)Mbp>/Kif9<em1(IMPC)Mbp>	C57BL/6N-Kif9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461378	F	MP:0000601	small liver	Kif9<em1(IMPC)Mbp>/Kif9<em1(IMPC)Mbp>	C57BL/6N-Kif9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461378	M	MP:0000692	small spleen	Kif9<em1(IMPC)Mbp>/Kif9<em1(IMPC)Mbp>	C57BL/6N-Kif9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461379	M	MP:0001417	decreased exploration in new environment	Kifc1<em1(IMPC)Bay>/Kifc1<em1(IMPC)Bay>	C57BL/6N-Kifc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461379	F	MP:0001399	hyperactivity	Kifc1<em1(IMPC)Bay>/Kifc1<em1(IMPC)Bay>	C57BL/6N-Kifc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461380	M	MP:0005561	increased mean corpuscular hemoglobin	Klf16<em1(IMPC)J>/Klf16<+>	C57BL/6NJ-Klf16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461380	M	MP:0002590	increased mean corpuscular volume	Klf16<em1(IMPC)J>/Klf16<+>	C57BL/6NJ-Klf16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461380	M	MP:0005560	decreased circulating glucose level	Klf16<em1(IMPC)J>/Klf16<+>	C57BL/6NJ-Klf16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461380	M	MP:0010392	prolonged QRS complex duration	Klf16<em1(IMPC)J>/Klf16<+>	C57BL/6NJ-Klf16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461380	M	MP:0001284	absent vibrissae	Klf16<em1(IMPC)J>/Klf16<+>	C57BL/6NJ-Klf16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461380	F	MP:0001566	increased circulating phosphate level	Klf16<em1(IMPC)J>/Klf16<+>	C57BL/6NJ-Klf16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461380	M	MP:0000367	abnormal coat/ hair morphology	Klf16<em1(IMPC)J>/Klf16<+>	C57BL/6NJ-Klf16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461380	M	MP:0000221	decreased leukocyte cell number	Klf16<em1(IMPC)J>/Klf16<+>	C57BL/6NJ-Klf16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461382	M	MP:0002768	small adrenal glands	Klhl12<em1(IMPC)Tcp>/Klhl12<em1(IMPC)Tcp>	C57BL/6N-Klhl12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461382	F	MP:0001258	decreased body length	Klhl12<em1(IMPC)Tcp>/Klhl12<em1(IMPC)Tcp>	C57BL/6N-Klhl12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461382	M	MP:0000157	abnormal sternum morphology	Klhl12<em1(IMPC)Tcp>/Klhl12<em1(IMPC)Tcp>	C57BL/6N-Klhl12<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461383	M	MP:0005576	decreased pulmonary ventilation	Klk4<tm1.1(KOMP)Vlcg>/Klk4<tm1.1(KOMP)Vlcg>	C57BL/6N-Klk4<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461384	M	MP:0000689	abnormal spleen morphology	Klk8<em1(IMPC)Ccpcz>/Klk8<em1(IMPC)Ccpcz>	C57BL/6N-Klk8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461384	M	MP:0000691	enlarged spleen	Klk8<em1(IMPC)Ccpcz>/Klk8<em1(IMPC)Ccpcz>	C57BL/6N-Klk8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461384	M	MP:0005016	decreased lymphocyte cell number	Klk8<em1(IMPC)Ccpcz>/Klk8<em1(IMPC)Ccpcz>	C57BL/6N-Klk8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461384	M	MP:0002135	abnormal kidney morphology	Klk8<em1(IMPC)Ccpcz>/Klk8<em1(IMPC)Ccpcz>	C57BL/6N-Klk8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461387	F	MP:0005553	increased circulating creatinine level	Klrc3<em1(IMPC)Wtsi>/Klrc3<+>	C57BL/6N-Klrc3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461388	M	MP:0001147	small testis	Kpna2<em1(IMPC)Mbp>/Kpna2<+>	C57BL/6N-Kpna2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461388	F	MP:0005278	abnormal cholesterol homeostasis	Kpna2<em1(IMPC)Mbp>/Kpna2<+>	C57BL/6N-Kpna2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461388	M	MP:0002135	abnormal kidney morphology	Kpna2<em1(IMPC)Mbp>/Kpna2<+>	C57BL/6N-Kpna2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461388	M	MP:0001146	abnormal testis morphology	Kpna2<em1(IMPC)Mbp>/Kpna2<+>	C57BL/6N-Kpna2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461388	M	MP:0002092	abnormal eye morphology	Kpna2<em1(IMPC)Mbp>/Kpna2<+>	C57BL/6N-Kpna2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461388	M	MP:0002989	small kidney	Kpna2<em1(IMPC)Mbp>/Kpna2<+>	C57BL/6N-Kpna2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461388	F	MP:0001402	decreased locomotor activity	Kpna2<em1(IMPC)Mbp>/Kpna2<+>	C57BL/6N-Kpna2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461389	M	MP:0001488	increased startle reflex	Kpna4<em1(IMPC)J>/Kpna4<em1(IMPC)J>	C57BL/6NJ-Kpna4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461390	F	MP:0000208	decreased hematocrit	Krt17<tm1.1(KOMP)Vlcg>/Krt17<+>	C57BL/6N-Krt17<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461390	M	MP:0002941	increased circulating alanine transaminase level	Krt17<tm1.1(KOMP)Vlcg>/Krt17<+>	C57BL/6N-Krt17<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461391	M	MP:0002833	increased heart weight	Krt74<tm1b(EUCOMM)Wtsi>/Krt74<tm1b(EUCOMM)Wtsi>	C57BL/6N-Krt74<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6461392	M	MP:0010024	increased total body fat amount	Krt75<em1(IMPC)Mbp>/Krt75<em1(IMPC)Mbp>	C57BL/6N-Krt75<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461394	F	MP:0005560	decreased circulating glucose level	Krt80<em1(IMPC)J>/Krt80<em1(IMPC)J>	C57BL/6NJ-Krt80<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461394	F	MP:0001399	hyperactivity	Krt80<em1(IMPC)J>/Krt80<em1(IMPC)J>	C57BL/6NJ-Krt80<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461394	F	MP:0002574	increased vertical activity	Krt80<em1(IMPC)J>/Krt80<em1(IMPC)J>	C57BL/6NJ-Krt80<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461395	M	MP:0010024	increased total body fat amount	Kti12<tm1.1(KOMP)Vlcg>/Kti12<+>	C57BL/6N-Kti12<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461395	M	MP:0000063	decreased bone mineral density	Kti12<tm1.1(KOMP)Vlcg>/Kti12<+>	C57BL/6N-Kti12<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461395	M	MP:0010124	decreased bone mineral content	Kti12<tm1.1(KOMP)Vlcg>/Kti12<+>	C57BL/6N-Kti12<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461395	M	MP:0003961	decreased lean body mass	Kti12<tm1.1(KOMP)Vlcg>/Kti12<+>	C57BL/6N-Kti12<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461396	F	MP:0000218	increased leukocyte cell number	Lamp1<em1(IMPC)Mbp>/Lamp1<em1(IMPC)Mbp>	C57BL/6N-Lamp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461396	F	MP:0000266	abnormal heart morphology	Lamp1<em1(IMPC)Mbp>/Lamp1<em1(IMPC)Mbp>	C57BL/6N-Lamp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461396	F	MP:0005013	increased lymphocyte cell number	Lamp1<em1(IMPC)Mbp>/Lamp1<em1(IMPC)Mbp>	C57BL/6N-Lamp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461396	M	MP:0000692	small spleen	Lamp1<em1(IMPC)Mbp>/Lamp1<em1(IMPC)Mbp>	C57BL/6N-Lamp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461396	F	MP:0002989	small kidney	Lamp1<em1(IMPC)Mbp>/Lamp1<em1(IMPC)Mbp>	C57BL/6N-Lamp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461396	F	MP:0001566	increased circulating phosphate level	Lamp1<em1(IMPC)Mbp>/Lamp1<em1(IMPC)Mbp>	C57BL/6N-Lamp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461396	F	MP:0002188	small heart	Lamp1<em1(IMPC)Mbp>/Lamp1<em1(IMPC)Mbp>	C57BL/6N-Lamp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461396	F	MP:0002135	abnormal kidney morphology	Lamp1<em1(IMPC)Mbp>/Lamp1<em1(IMPC)Mbp>	C57BL/6N-Lamp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461397	F	MP:0009709	hydrometra	Lamtor1<tm1b(KOMP)Wtsi>/Lamtor1<+>	C57BL/6N-Lamtor1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6461397	F	MP:0001102	small superior vagus ganglion	Lamtor1<tm1b(KOMP)Wtsi>/Lamtor1<+>	C57BL/6N-Lamtor1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6461397	M	MP:0001146	abnormal testis morphology	Lamtor1<tm1b(KOMP)Wtsi>/Lamtor1<+>	C57BL/6N-Lamtor1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6461397	F	MP:0004832	enlarged ovary	Lamtor1<tm1b(KOMP)Wtsi>/Lamtor1<+>	C57BL/6N-Lamtor1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6461397	F	MP:0001126	abnormal ovary morphology	Lamtor1<tm1b(KOMP)Wtsi>/Lamtor1<+>	C57BL/6N-Lamtor1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6461397	M	MP:0004931	enlarged epididymis	Lamtor1<tm1b(KOMP)Wtsi>/Lamtor1<+>	C57BL/6N-Lamtor1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6461397	M	MP:0002631	abnormal epididymis morphology	Lamtor1<tm1b(KOMP)Wtsi>/Lamtor1<+>	C57BL/6N-Lamtor1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6461397	M	MP:0001148	enlarged testis	Lamtor1<tm1b(KOMP)Wtsi>/Lamtor1<+>	C57BL/6N-Lamtor1<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:6461399	M	MP:0002059	abnormal seminal vesicle morphology	Larp1<em1(IMPC)Mbp>/Larp1<+>	C57BL/6N-Larp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461399	M	MP:0002135	abnormal kidney morphology	Larp1<em1(IMPC)Mbp>/Larp1<+>	C57BL/6N-Larp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461399	M	MP:0000274	enlarged heart	Larp1<em1(IMPC)Mbp>/Larp1<+>	C57BL/6N-Larp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461399	M	MP:0000186	decreased circulating HDL cholesterol level	Larp1<em1(IMPC)Mbp>/Larp1<+>	C57BL/6N-Larp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461399	M	MP:0000266	abnormal heart morphology	Larp1<em1(IMPC)Mbp>/Larp1<+>	C57BL/6N-Larp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461399	M	MP:0003068	enlarged kidney	Larp1<em1(IMPC)Mbp>/Larp1<+>	C57BL/6N-Larp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461399	F	MP:0002060	abnormal skin morphology	Larp1<em1(IMPC)Mbp>/Larp1<+>	C57BL/6N-Larp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461399	M	MP:0001147	small testis	Larp1<em1(IMPC)Mbp>/Larp1<+>	C57BL/6N-Larp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461399	M	MP:0003642	absent seminal vesicle	Larp1<em1(IMPC)Mbp>/Larp1<+>	C57BL/6N-Larp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461399	M	MP:0000598	abnormal liver morphology	Larp1<em1(IMPC)Mbp>/Larp1<+>	C57BL/6N-Larp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461399	M	MP:0005179	decreased circulating cholesterol level	Larp1<em1(IMPC)Mbp>/Larp1<+>	C57BL/6N-Larp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461399	M	MP:0011874	enlarged urinary bladder	Larp1<em1(IMPC)Mbp>/Larp1<+>	C57BL/6N-Larp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461399	M	MP:0002997	enlarged seminal vesicle	Larp1<em1(IMPC)Mbp>/Larp1<+>	C57BL/6N-Larp1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461402	F	MP:0010511	shortened PR interval	Limd1<em1(IMPC)H>/Limd1<em1(IMPC)H>	C57BL/6NTac-Limd1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461402	M	MP:0010053	decreased grip strength	Limd1<em1(IMPC)H>/Limd1<em1(IMPC)H>	C57BL/6NTac-Limd1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461402	F	MP:0002606	increased basophil cell number	Limd1<em1(IMPC)H>/Limd1<em1(IMPC)H>	C57BL/6NTac-Limd1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461402	F	MP:0002599	increased mean platelet volume	Limd1<em1(IMPC)H>/Limd1<em1(IMPC)H>	C57BL/6NTac-Limd1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461402	F	MP:0002966	decreased circulating alkaline phosphatase level	Limd1<em1(IMPC)H>/Limd1<em1(IMPC)H>	C57BL/6NTac-Limd1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461402	F	MP:0009142	decreased prepulse inhibition	Limd1<em1(IMPC)H>/Limd1<em1(IMPC)H>	C57BL/6NTac-Limd1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461402	F	MP:0010052	increased grip strength	Limd1<em1(IMPC)H>/Limd1<em1(IMPC)H>	C57BL/6NTac-Limd1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461403	M	MP:0001488	increased startle reflex	Llgl2<tm1b(KOMP)Wtsi>/Llgl2<+>	C57BL/6N-Llgl2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461403	M	MP:0000186	decreased circulating HDL cholesterol level	Llgl2<tm1b(KOMP)Wtsi>/Llgl2<+>	C57BL/6N-Llgl2<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461404	F	MP:0009142	decreased prepulse inhibition	Lmcd1<em1(IMPC)J>/Lmcd1<em1(IMPC)J>	C57BL/6NJ-Lmcd1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461404	F	MP:0010124	decreased bone mineral content	Lmcd1<em1(IMPC)J>/Lmcd1<em1(IMPC)J>	C57BL/6NJ-Lmcd1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461404	F	MP:0001289	persistence of hyaloid vascular system	Lmcd1<em1(IMPC)J>/Lmcd1<em1(IMPC)J>	C57BL/6NJ-Lmcd1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461404	F	MP:0001304	cataract	Lmcd1<em1(IMPC)J>/Lmcd1<em1(IMPC)J>	C57BL/6NJ-Lmcd1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461405	M	MP:0002757	decreased vertical activity	Lmo1<tm1b(KOMP)Mbp>/Lmo1<tm1b(KOMP)Mbp>	C57BL/6N-Lmo1<tm1b(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:6461405	M	MP:0020870	decreased thigmotaxis	Lmo1<tm1b(KOMP)Mbp>/Lmo1<tm1b(KOMP)Mbp>	C57BL/6N-Lmo1<tm1b(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:6461405	F	MP:0001325	abnormal retina morphology	Lmo1<tm1b(KOMP)Mbp>/Lmo1<tm1b(KOMP)Mbp>	C57BL/6N-Lmo1<tm1b(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:6461405	M	MP:0001364	decreased anxiety-related response	Lmo1<tm1b(KOMP)Mbp>/Lmo1<tm1b(KOMP)Mbp>	C57BL/6N-Lmo1<tm1b(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:6461405	M	MP:0004924	abnormal behavior	Lmo1<tm1b(KOMP)Mbp>/Lmo1<tm1b(KOMP)Mbp>	C57BL/6N-Lmo1<tm1b(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:6461406	F	MP:0008206	increased B-2 B cell number	Lratd2<em1(IMPC)Ccpcz>/Lratd2<em1(IMPC)Ccpcz>	C57BL/6N-Lratd2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461406	M	MP:0010379	decreased respiratory quotient	Lratd2<em1(IMPC)Ccpcz>/Lratd2<em1(IMPC)Ccpcz>	C57BL/6N-Lratd2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461406	F	MP:0005012	decreased eosinophil cell number	Lratd2<em1(IMPC)Ccpcz>/Lratd2<em1(IMPC)Ccpcz>	C57BL/6N-Lratd2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461407	F	MP:0002092	abnormal eye morphology	Lrch2<em1(IMPC)Mbp>/Lrch2<em1(IMPC)Mbp>	C57BL/6N-Lrch2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461407	F	MP:0001293	anophthalmia	Lrch2<em1(IMPC)Mbp>/Lrch2<em1(IMPC)Mbp>	C57BL/6N-Lrch2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461408	M	MP:0002631	abnormal epididymis morphology	Lrit3<em1(IMPC)Mbp>/Lrit3<em1(IMPC)Mbp>	C57BL/6N-Lrit3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461408	M	MP:0004931	enlarged epididymis	Lrit3<em1(IMPC)Mbp>/Lrit3<em1(IMPC)Mbp>	C57BL/6N-Lrit3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461410	F	MP:0000367	abnormal coat/ hair morphology	Lrrc41<em1(IMPC)J>/Lrrc41<em1(IMPC)J>	C57BL/6NJ-Lrrc41<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461410	F	MP:0001399	hyperactivity	Lrrc41<em1(IMPC)J>/Lrrc41<em1(IMPC)J>	C57BL/6NJ-Lrrc41<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461410	M	MP:0000194	increased circulating calcium level	Lrrc41<em1(IMPC)J>/Lrrc41<em1(IMPC)J>	C57BL/6NJ-Lrrc41<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461410	F	MP:0002968	increased circulating alkaline phosphatase level	Lrrc41<em1(IMPC)J>/Lrrc41<em1(IMPC)J>	C57BL/6NJ-Lrrc41<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461410	M	MP:0003960	increased lean body mass	Lrrc41<em1(IMPC)J>/Lrrc41<em1(IMPC)J>	C57BL/6NJ-Lrrc41<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461410	F	MP:0005559	increased circulating glucose level	Lrrc41<em1(IMPC)J>/Lrrc41<em1(IMPC)J>	C57BL/6NJ-Lrrc41<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461411	M	MP:0002060	abnormal skin morphology	Lrrc56<em1(IMPC)Tcp>/Lrrc56<em1(IMPC)Tcp>	C57BL/6N-Lrrc56<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461411	M	MP:0000702	enlarged lymph nodes	Lrrc56<em1(IMPC)Tcp>/Lrrc56<em1(IMPC)Tcp>	C57BL/6N-Lrrc56<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461411	M	MP:0001925	male infertility	Lrrc56<em1(IMPC)Tcp>/Lrrc56<em1(IMPC)Tcp>	C57BL/6N-Lrrc56<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461411	M	MP:0001258	decreased body length	Lrrc56<em1(IMPC)Tcp>/Lrrc56<em1(IMPC)Tcp>	C57BL/6N-Lrrc56<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461411	M	MP:0001175	abnormal lung morphology	Lrrc56<em1(IMPC)Tcp>/Lrrc56<em1(IMPC)Tcp>	C57BL/6N-Lrrc56<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461411	M	MP:0002941	increased circulating alanine transaminase level	Lrrc56<em1(IMPC)Tcp>/Lrrc56<em1(IMPC)Tcp>	C57BL/6N-Lrrc56<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461412	M	MP:0000689	abnormal spleen morphology	Lrrc8c<em1(IMPC)Mbp>/Lrrc8c<em1(IMPC)Mbp>	C57BL/6N-Lrrc8c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461412	F	MP:0002092	abnormal eye morphology	Lrrc8c<em1(IMPC)Mbp>/Lrrc8c<em1(IMPC)Mbp>	C57BL/6N-Lrrc8c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461412	M	MP:0001146	abnormal testis morphology	Lrrc8c<em1(IMPC)Mbp>/Lrrc8c<em1(IMPC)Mbp>	C57BL/6N-Lrrc8c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461412	M	MP:0005419	decreased circulating serum albumin level	Lrrc8c<em1(IMPC)Mbp>/Lrrc8c<em1(IMPC)Mbp>	C57BL/6N-Lrrc8c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461412	M	MP:0000195	decreased circulating calcium level	Lrrc8c<em1(IMPC)Mbp>/Lrrc8c<em1(IMPC)Mbp>	C57BL/6N-Lrrc8c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461412	M	MP:0001147	small testis	Lrrc8c<em1(IMPC)Mbp>/Lrrc8c<em1(IMPC)Mbp>	C57BL/6N-Lrrc8c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461412	M	MP:0011110	preweaning lethality, incomplete penetrance	Lrrc8c<em1(IMPC)Mbp>/Lrrc8c<em1(IMPC)Mbp>	C57BL/6N-Lrrc8c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461413	M	MP:0002135	abnormal kidney morphology	Lrrtm2<em1(IMPC)Mbp>/Lrrtm2<em1(IMPC)Mbp>	C57BL/6N-Lrrtm2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461413	M	MP:0000702	enlarged lymph nodes	Lrrtm2<em1(IMPC)Mbp>/Lrrtm2<em1(IMPC)Mbp>	C57BL/6N-Lrrtm2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461413	M	MP:0002060	abnormal skin morphology	Lrrtm2<em1(IMPC)Mbp>/Lrrtm2<em1(IMPC)Mbp>	C57BL/6N-Lrrtm2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461413	M	MP:0003068	enlarged kidney	Lrrtm2<em1(IMPC)Mbp>/Lrrtm2<em1(IMPC)Mbp>	C57BL/6N-Lrrtm2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461413	M	MP:0000538	abnormal urinary bladder morphology	Lrrtm2<em1(IMPC)Mbp>/Lrrtm2<em1(IMPC)Mbp>	C57BL/6N-Lrrtm2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461413	M	MP:0009552	urinary bladder obstruction	Lrrtm2<em1(IMPC)Mbp>/Lrrtm2<em1(IMPC)Mbp>	C57BL/6N-Lrrtm2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461413	M	MP:0002339	abnormal lymph node morphology	Lrrtm2<em1(IMPC)Mbp>/Lrrtm2<em1(IMPC)Mbp>	C57BL/6N-Lrrtm2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461413	M	MP:0001175	abnormal lung morphology	Lrrtm2<em1(IMPC)Mbp>/Lrrtm2<em1(IMPC)Mbp>	C57BL/6N-Lrrtm2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461413	F	MP:0005084	abnormal gallbladder morphology	Lrrtm2<em1(IMPC)Mbp>/Lrrtm2<em1(IMPC)Mbp>	C57BL/6N-Lrrtm2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461414	M	MP:0005575	increased pulmonary ventilation	Lta<tm1.1(KOMP)Vlcg>/Lta<tm1.1(KOMP)Vlcg>	C57BL/6N-Lta<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461414	M	MP:0012124	increased bronchoconstrictive response	Lta<tm1.1(KOMP)Vlcg>/Lta<tm1.1(KOMP)Vlcg>	C57BL/6N-Lta<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461415	F	MP:0000692	small spleen	M6pr<em1(IMPC)Mbp>/M6pr<em1(IMPC)Mbp>	C57BL/6N-M6pr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461415	F	MP:0004924	abnormal behavior	M6pr<em1(IMPC)Mbp>/M6pr<em1(IMPC)Mbp>	C57BL/6N-M6pr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461415	F	MP:0001402	decreased locomotor activity	M6pr<em1(IMPC)Mbp>/M6pr<em1(IMPC)Mbp>	C57BL/6N-M6pr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461415	F	MP:0001364	decreased anxiety-related response	M6pr<em1(IMPC)Mbp>/M6pr<em1(IMPC)Mbp>	C57BL/6N-M6pr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461415	M	MP:0006203	eye hemorrhage	M6pr<em1(IMPC)Mbp>/M6pr<em1(IMPC)Mbp>	C57BL/6N-M6pr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461415	F	MP:0020870	decreased thigmotaxis	M6pr<em1(IMPC)Mbp>/M6pr<em1(IMPC)Mbp>	C57BL/6N-M6pr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461416	F	MP:0002092	abnormal eye morphology	Mab21l2<em1(IMPC)Mbp>/Mab21l2<+>	C57BL/6N-Mab21l2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461416	F	MP:0001293	anophthalmia	Mab21l2<em1(IMPC)Mbp>/Mab21l2<+>	C57BL/6N-Mab21l2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461416	M	MP:0005554	decreased circulating creatinine level	Mab21l2<em1(IMPC)Mbp>/Mab21l2<+>	C57BL/6N-Mab21l2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461416	F	MP:0002151	abnormal neural tube morphology	Mab21l2<em1(IMPC)Mbp>/Mab21l2<+>	C57BL/6N-Mab21l2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461416	M	MP:0003231	abnormal placenta vasculature	Mab21l2<em1(IMPC)Mbp>/Mab21l2<+>	C57BL/6N-Mab21l2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461417	M	MP:0001529	abnormal vocalization	Mak16<em1(IMPC)J>/Mak16<+>	C57BL/6NJ-Mak16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461418	M	MP:0005567	decreased circulating total protein level	Man2b2<tm1b(KOMP)Wtsi>/Man2b2<tm1b(KOMP)Wtsi>	C57BL/6N-Man2b2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461418	M	MP:0010088	decreased circulating fructosamine level	Man2b2<tm1b(KOMP)Wtsi>/Man2b2<tm1b(KOMP)Wtsi>	C57BL/6N-Man2b2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461418	M	MP:0005419	decreased circulating serum albumin level	Man2b2<tm1b(KOMP)Wtsi>/Man2b2<tm1b(KOMP)Wtsi>	C57BL/6N-Man2b2<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461419	M	MP:0005344	increased circulating bilirubin level	Mansc4<tm1b(KOMP)Wtsi>/Mansc4<tm1b(KOMP)Wtsi>	C57BL/6N-Mansc4<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461420	M	MP:0005553	increased circulating creatinine level	Mapk13<em1(IMPC)Hmgu>/Mapk13<em1(IMPC)Hmgu>	C57BL/6N-Mapk13<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461421	M	MP:0002968	increased circulating alkaline phosphatase level	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	F	MP:0020421	increased freezing behavior	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	M	MP:0001147	small testis	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	M	MP:0010936	decreased airway resistance	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	M	MP:0013279	increased fasting circulating glucose level	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	F	MP:0005012	decreased eosinophil cell number	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	M	MP:0011045	decreased lung elastance	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	F	MP:0005293	impaired glucose tolerance	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	M	MP:0009142	decreased prepulse inhibition	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	M	MP:0000443	abnormal snout morphology	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	F	MP:0001399	hyperactivity	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	M	MP:0001146	abnormal testis morphology	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	M	MP:0001925	male infertility	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461421	M	MP:0005343	increased circulating aspartate transaminase level	Marchf6<tm1b(EUCOMM)Hmgu>/Marchf6<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf6<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6461422	F	MP:0000639	abnormal adrenal gland morphology	Mb21d2<em1(IMPC)Mbp>/Mb21d2<em1(IMPC)Mbp>	C57BL/6N-Mb21d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461422	M	MP:0000689	abnormal spleen morphology	Mb21d2<em1(IMPC)Mbp>/Mb21d2<em1(IMPC)Mbp>	C57BL/6N-Mb21d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461423	F	MP:0003731	abnormal retina outer nuclear layer morphology	Mccc1<em1(IMPC)Bay>/Mccc1<+>	C57BL/6N-Mccc1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6461424	F	MP:0002188	small heart	Mcl1<em1(IMPC)Mbp>/Mcl1<+>	C57BL/6N-Mcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461424	M	MP:0002339	abnormal lymph node morphology	Mcl1<em1(IMPC)Mbp>/Mcl1<+>	C57BL/6N-Mcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461424	F	MP:0010052	increased grip strength	Mcl1<em1(IMPC)Mbp>/Mcl1<+>	C57BL/6N-Mcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461424	F	MP:0001297	microphthalmia	Mcl1<em1(IMPC)Mbp>/Mcl1<+>	C57BL/6N-Mcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461424	F	MP:0000266	abnormal heart morphology	Mcl1<em1(IMPC)Mbp>/Mcl1<+>	C57BL/6N-Mcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461424	M	MP:0000702	enlarged lymph nodes	Mcl1<em1(IMPC)Mbp>/Mcl1<+>	C57BL/6N-Mcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461424	F	MP:0001293	anophthalmia	Mcl1<em1(IMPC)Mbp>/Mcl1<+>	C57BL/6N-Mcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461424	M	MP:0000692	small spleen	Mcl1<em1(IMPC)Mbp>/Mcl1<+>	C57BL/6N-Mcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461425	M	MP:0000063	decreased bone mineral density	Mcmbp<em1(IMPC)J>/Mcmbp<+>	C57BL/6NJ-Mcmbp<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461425	M	MP:0002591	decreased mean corpuscular volume	Mcmbp<em1(IMPC)J>/Mcmbp<+>	C57BL/6NJ-Mcmbp<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461425	M	MP:0005562	decreased mean corpuscular hemoglobin	Mcmbp<em1(IMPC)J>/Mcmbp<+>	C57BL/6NJ-Mcmbp<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461425	M	MP:0003961	decreased lean body mass	Mcmbp<em1(IMPC)J>/Mcmbp<+>	C57BL/6NJ-Mcmbp<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461426	F	MP:0002953	thick ventricular wall	Mdh1<em1(IMPC)Bay>/Mdh1<+>	C57BL/6N-Mdh1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6461426	F	MP:0001417	decreased exploration in new environment	Mdh1<em1(IMPC)Bay>/Mdh1<+>	C57BL/6N-Mdh1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6461428	M	MP:0002941	increased circulating alanine transaminase level	Med12l<em1(IMPC)J>/Med12l<em1(IMPC)J>	C57BL/6NJ-Med12l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461428	F	MP:0001392	abnormal locomotor behavior	Med12l<em1(IMPC)J>/Med12l<em1(IMPC)J>	C57BL/6NJ-Med12l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461428	F	MP:0010053	decreased grip strength	Med12l<em1(IMPC)J>/Med12l<em1(IMPC)J>	C57BL/6NJ-Med12l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461428	F	MP:0001319	irregularly shaped pupil	Med12l<em1(IMPC)J>/Med12l<em1(IMPC)J>	C57BL/6NJ-Med12l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461430	F	MP:0013279	increased fasting circulating glucose level	Mettl6<em1(IMPC)J>/Mettl6<em1(IMPC)J>	C57BL/6NJ-Mettl6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461430	F	MP:0001529	abnormal vocalization	Mettl6<em1(IMPC)J>/Mettl6<em1(IMPC)J>	C57BL/6NJ-Mettl6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461431	M	MP:0011952	decreased cardiac stroke volume	Mgat1<tm1b(EUCOMM)Hmgu>/Mgat1<+>	C57BL/6N-Mgat1<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6461432	F	MP:0001402	decreased locomotor activity	Mgll<em1(IMPC)Hmgu>/Mgll<em1(IMPC)Hmgu>	C57BL/6N-Mgll<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461433	F	MP:0000692	small spleen	Mgst2<em1(IMPC)Mbp>/Mgst2<em1(IMPC)Mbp>	C57BL/6N-Mgst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461433	M	MP:0002989	small kidney	Mgst2<em1(IMPC)Mbp>/Mgst2<em1(IMPC)Mbp>	C57BL/6N-Mgst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461433	F	MP:0000689	abnormal spleen morphology	Mgst2<em1(IMPC)Mbp>/Mgst2<em1(IMPC)Mbp>	C57BL/6N-Mgst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461433	M	MP:0002060	abnormal skin morphology	Mgst2<em1(IMPC)Mbp>/Mgst2<em1(IMPC)Mbp>	C57BL/6N-Mgst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461433	F	MP:0000494	abnormal cecum morphology	Mgst2<em1(IMPC)Mbp>/Mgst2<em1(IMPC)Mbp>	C57BL/6N-Mgst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461433	F	MP:0009476	enlarged cecum	Mgst2<em1(IMPC)Mbp>/Mgst2<em1(IMPC)Mbp>	C57BL/6N-Mgst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461433	M	MP:0002135	abnormal kidney morphology	Mgst2<em1(IMPC)Mbp>/Mgst2<em1(IMPC)Mbp>	C57BL/6N-Mgst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461433	F	MP:0000266	abnormal heart morphology	Mgst2<em1(IMPC)Mbp>/Mgst2<em1(IMPC)Mbp>	C57BL/6N-Mgst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461433	F	MP:0002188	small heart	Mgst2<em1(IMPC)Mbp>/Mgst2<em1(IMPC)Mbp>	C57BL/6N-Mgst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461433	F	MP:0002092	abnormal eye morphology	Mgst2<em1(IMPC)Mbp>/Mgst2<em1(IMPC)Mbp>	C57BL/6N-Mgst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461433	F	MP:0001293	anophthalmia	Mgst2<em1(IMPC)Mbp>/Mgst2<em1(IMPC)Mbp>	C57BL/6N-Mgst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461433	M	MP:0001417	decreased exploration in new environment	Mgst2<em1(IMPC)Mbp>/Mgst2<em1(IMPC)Mbp>	C57BL/6N-Mgst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461434	F	MP:0000639	abnormal adrenal gland morphology	Mief1<em1(IMPC)Mbp>/Mief1<em1(IMPC)Mbp>	C57BL/6N-Mief1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461434	F	MP:0000266	abnormal heart morphology	Mief1<em1(IMPC)Mbp>/Mief1<em1(IMPC)Mbp>	C57BL/6N-Mief1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461434	F	MP:0000274	enlarged heart	Mief1<em1(IMPC)Mbp>/Mief1<em1(IMPC)Mbp>	C57BL/6N-Mief1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	F	MP:0000689	abnormal spleen morphology	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	F	MP:0001258	decreased body length	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	M	MP:0002339	abnormal lymph node morphology	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	F	MP:0002989	small kidney	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	F	MP:0010124	decreased bone mineral content	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	F	MP:0003795	abnormal bone structure	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	F	MP:0000274	enlarged heart	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	M	MP:0010053	decreased grip strength	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	F	MP:0000691	enlarged spleen	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	F	MP:0000470	abnormal stomach morphology	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	F	MP:0003883	enlarged stomach	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	M	MP:0000702	enlarged lymph nodes	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	F	MP:0002135	abnormal kidney morphology	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	M	MP:0002059	abnormal seminal vesicle morphology	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461436	F	MP:0000266	abnormal heart morphology	Mmp2<em1(IMPC)Mbp>/Mmp2<em1(IMPC)Mbp>	C57BL/6N-Mmp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461437	M	MP:0001488	increased startle reflex	Mob2<tm1b(KOMP)Wtsi>/Mob2<+>	C57BL/6N-Mob2<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6461438	M	MP:0001402	decreased locomotor activity	Mogat2<em1(IMPC)Mbp>/Mogat2<em1(IMPC)Mbp>	C57BL/6N-Mogat2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461438	F	MP:0009142	decreased prepulse inhibition	Mogat2<em1(IMPC)Mbp>/Mogat2<em1(IMPC)Mbp>	C57BL/6N-Mogat2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461438	M	MP:0000691	enlarged spleen	Mogat2<em1(IMPC)Mbp>/Mogat2<em1(IMPC)Mbp>	C57BL/6N-Mogat2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461438	M	MP:0001147	small testis	Mogat2<em1(IMPC)Mbp>/Mogat2<em1(IMPC)Mbp>	C57BL/6N-Mogat2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461438	M	MP:0001157	small seminal vesicle	Mogat2<em1(IMPC)Mbp>/Mogat2<em1(IMPC)Mbp>	C57BL/6N-Mogat2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461438	F	MP:0002060	abnormal skin morphology	Mogat2<em1(IMPC)Mbp>/Mogat2<em1(IMPC)Mbp>	C57BL/6N-Mogat2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461438	M	MP:0001146	abnormal testis morphology	Mogat2<em1(IMPC)Mbp>/Mogat2<em1(IMPC)Mbp>	C57BL/6N-Mogat2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461438	M	MP:0000689	abnormal spleen morphology	Mogat2<em1(IMPC)Mbp>/Mogat2<em1(IMPC)Mbp>	C57BL/6N-Mogat2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461438	M	MP:0002059	abnormal seminal vesicle morphology	Mogat2<em1(IMPC)Mbp>/Mogat2<em1(IMPC)Mbp>	C57BL/6N-Mogat2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461439	M	MP:0002833	increased heart weight	Mon2<em1(IMPC)J>/Mon2<+>	C57BL/6NJ-Mon2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461440	M	MP:0000208	decreased hematocrit	Morc3<tm1b(EUCOMM)Hmgu>/Morc3<+>	C57BL/6N-Morc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461440	M	MP:0001417	decreased exploration in new environment	Morc3<tm1b(EUCOMM)Hmgu>/Morc3<+>	C57BL/6N-Morc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461440	M	MP:0012362	increased large unstained cell number	Morc3<tm1b(EUCOMM)Hmgu>/Morc3<+>	C57BL/6N-Morc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461440	M	MP:0005016	decreased lymphocyte cell number	Morc3<tm1b(EUCOMM)Hmgu>/Morc3<+>	C57BL/6N-Morc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461440	M	MP:0002941	increased circulating alanine transaminase level	Morc3<tm1b(EUCOMM)Hmgu>/Morc3<+>	C57BL/6N-Morc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461440	M	MP:0002875	decreased erythrocyte cell number	Morc3<tm1b(EUCOMM)Hmgu>/Morc3<+>	C57BL/6N-Morc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461440	M	MP:0005343	increased circulating aspartate transaminase level	Morc3<tm1b(EUCOMM)Hmgu>/Morc3<+>	C57BL/6N-Morc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461440	M	MP:0002874	decreased hemoglobin content	Morc3<tm1b(EUCOMM)Hmgu>/Morc3<+>	C57BL/6N-Morc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461440	M	MP:0000219	increased neutrophil cell number	Morc3<tm1b(EUCOMM)Hmgu>/Morc3<+>	C57BL/6N-Morc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461440	M	MP:0000220	increased monocyte cell number	Morc3<tm1b(EUCOMM)Hmgu>/Morc3<+>	C57BL/6N-Morc3<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461441	F	MP:0010053	decreased grip strength	Mphosph10<em1(IMPC)J>/Mphosph10<+>	C57BL/6NJ-Mphosph10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461442	F	MP:0009141	increased prepulse inhibition	Mphosph9<tm1e.1(EUCOMM)Hmgu>/Mphosph9<tm1e.1(EUCOMM)Hmgu>	C57BL/6N-Mphosph9<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6461442	M	MP:0011965	decreased total retina thickness	Mphosph9<tm1e.1(EUCOMM)Hmgu>/Mphosph9<tm1e.1(EUCOMM)Hmgu>	C57BL/6N-Mphosph9<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6461442	F	MP:0008806	increased circulating amylase level	Mphosph9<tm1e.1(EUCOMM)Hmgu>/Mphosph9<tm1e.1(EUCOMM)Hmgu>	C57BL/6N-Mphosph9<tm1e.1(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6461443	M	MP:0005573	increased pulmonary respiratory rate	Mpig6b<tm1.1(KOMP)Vlcg>/Mpig6b<tm1.1(KOMP)Vlcg>	C57BL/6N-Mpig6b<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461444	F	MP:0010053	decreased grip strength	Mprip<em1(IMPC)J>/Mprip<+>	C57BL/6NJ-Mprip<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461444	F	MP:0002968	increased circulating alkaline phosphatase level	Mprip<em1(IMPC)J>/Mprip<+>	C57BL/6NJ-Mprip<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461444	F	MP:0001392	abnormal locomotor behavior	Mprip<em1(IMPC)J>/Mprip<+>	C57BL/6NJ-Mprip<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461445	M	MP:0001258	decreased body length	Mreg<tm1b(EUCOMM)Hmgu>/Mreg<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mreg<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:6461445	M	MP:0002339	abnormal lymph node morphology	Mreg<tm1b(EUCOMM)Hmgu>/Mreg<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mreg<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:6461445	F	MP:0009142	decreased prepulse inhibition	Mreg<tm1b(EUCOMM)Hmgu>/Mreg<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mreg<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:6461446	M	MP:0001513	limb grasping	Mrgbp<em1(IMPC)J>/Mrgbp<+>	C57BL/6NJ-Mrgbp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461449	M	MP:0000274	enlarged heart	Msh3<em1(IMPC)Mbp>/Msh3<em1(IMPC)Mbp>	C57BL/6N-Msh3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461449	M	MP:0002135	abnormal kidney morphology	Msh3<em1(IMPC)Mbp>/Msh3<em1(IMPC)Mbp>	C57BL/6N-Msh3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461449	M	MP:0001304	cataract	Msh3<em1(IMPC)Mbp>/Msh3<em1(IMPC)Mbp>	C57BL/6N-Msh3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461449	F	MP:0002060	abnormal skin morphology	Msh3<em1(IMPC)Mbp>/Msh3<em1(IMPC)Mbp>	C57BL/6N-Msh3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461449	M	MP:0000266	abnormal heart morphology	Msh3<em1(IMPC)Mbp>/Msh3<em1(IMPC)Mbp>	C57BL/6N-Msh3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461449	M	MP:0003068	enlarged kidney	Msh3<em1(IMPC)Mbp>/Msh3<em1(IMPC)Mbp>	C57BL/6N-Msh3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461450	M	MP:0002874	decreased hemoglobin content	Msn<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Msn<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461450	M	MP:0002875	decreased erythrocyte cell number	Msn<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Msn<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461450	M	MP:0000208	decreased hematocrit	Msn<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Msn<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461450	M	MP:0005561	increased mean corpuscular hemoglobin	Msn<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Msn<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461450	M	MP:0006243	impaired pupillary reflex	Msn<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Msn<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461451	M	MP:0002626	increased heart rate	Mtg1<em1(IMPC)Bay>/Mtg1<+>	C57BL/6N-Mtg1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6461451	M	MP:0010507	shortened RR interval	Mtg1<em1(IMPC)Bay>/Mtg1<+>	C57BL/6N-Mtg1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6461455	F	MP:0009084	blind uterus	Mxd3<em1(IMPC)Mbp>/Mxd3<em1(IMPC)Mbp>	C57BL/6N-Mxd3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461456	F	MP:0002075	abnormal coat/hair pigmentation	Mxra8<em1(IMPC)J>/Mxra8<em1(IMPC)J>	C57BL/6NJ-Mxra8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461456	F	MP:0001399	hyperactivity	Mxra8<em1(IMPC)J>/Mxra8<em1(IMPC)J>	C57BL/6NJ-Mxra8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461459	M	MP:0000691	enlarged spleen	Myct1<em1(IMPC)Mbp>/Myct1<em1(IMPC)Mbp>	C57BL/6N-Myct1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461459	M	MP:0001293	anophthalmia	Myct1<em1(IMPC)Mbp>/Myct1<em1(IMPC)Mbp>	C57BL/6N-Myct1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461459	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Myct1<em1(IMPC)Mbp>/Myct1<em1(IMPC)Mbp>	C57BL/6N-Myct1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461459	F	MP:0010067	increased red blood cell distribution width	Myct1<em1(IMPC)Mbp>/Myct1<em1(IMPC)Mbp>	C57BL/6N-Myct1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461461	M	MP:0001552	increased circulating triglyceride level	Myo18b<em2(IMPC)Ics>/Myo18b<+>	C57BL/6N-Myo18b<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461463	F	MP:0002075	abnormal coat/hair pigmentation	Mypn<em1(IMPC)J>/Mypn<em1(IMPC)J>	C57BL/6NJ-Mypn<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461463	M	MP:0000221	decreased leukocyte cell number	Mypn<em1(IMPC)J>/Mypn<em1(IMPC)J>	C57BL/6NJ-Mypn<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461464	M	MP:0000702	enlarged lymph nodes	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0000689	abnormal spleen morphology	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0001146	abnormal testis morphology	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0002059	abnormal seminal vesicle morphology	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0002997	enlarged seminal vesicle	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0002075	abnormal coat/hair pigmentation	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0001891	hydrocephaly	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0002060	abnormal skin morphology	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0002339	abnormal lymph node morphology	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0000639	abnormal adrenal gland morphology	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0002989	small kidney	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0002135	abnormal kidney morphology	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0000598	abnormal liver morphology	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0002834	decreased heart weight	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0003068	enlarged kidney	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0001147	small testis	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0002152	abnormal brain morphology	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461464	M	MP:0000692	small spleen	Naa10<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Naa10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461465	M	MP:0005575	increased pulmonary ventilation	Nadsyn1<tm1b(KOMP)Wtsi>/Nadsyn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nadsyn1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6461465	F	MP:0005576	decreased pulmonary ventilation	Nadsyn1<tm1b(KOMP)Wtsi>/Nadsyn1<tm1b(KOMP)Wtsi>	C57BL/6N-Nadsyn1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6461467	M	MP:0010124	decreased bone mineral content	Ncbp1<em1(IMPC)J>/Ncbp1<+>	C57BL/6NJ-Ncbp1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461468	M	MP:0020870	decreased thigmotaxis	Ncf1<em1(IMPC)Mbp>/Ncf1<em1(IMPC)Mbp>	C57BL/6N-Ncf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461468	M	MP:0001364	decreased anxiety-related response	Ncf1<em1(IMPC)Mbp>/Ncf1<em1(IMPC)Mbp>	C57BL/6N-Ncf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461468	F	MP:0003604	single kidney	Ncf1<em1(IMPC)Mbp>/Ncf1<em1(IMPC)Mbp>	C57BL/6N-Ncf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461468	M	MP:0004924	abnormal behavior	Ncf1<em1(IMPC)Mbp>/Ncf1<em1(IMPC)Mbp>	C57BL/6N-Ncf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461468	F	MP:0002092	abnormal eye morphology	Ncf1<em1(IMPC)Mbp>/Ncf1<em1(IMPC)Mbp>	C57BL/6N-Ncf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461468	F	MP:0001175	abnormal lung morphology	Ncf1<em1(IMPC)Mbp>/Ncf1<em1(IMPC)Mbp>	C57BL/6N-Ncf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461468	M	MP:0000266	abnormal heart morphology	Ncf1<em1(IMPC)Mbp>/Ncf1<em1(IMPC)Mbp>	C57BL/6N-Ncf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461468	F	MP:0002060	abnormal skin morphology	Ncf1<em1(IMPC)Mbp>/Ncf1<em1(IMPC)Mbp>	C57BL/6N-Ncf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461468	M	MP:0001402	decreased locomotor activity	Ncf1<em1(IMPC)Mbp>/Ncf1<em1(IMPC)Mbp>	C57BL/6N-Ncf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461468	M	MP:0003068	enlarged kidney	Ncf1<em1(IMPC)Mbp>/Ncf1<em1(IMPC)Mbp>	C57BL/6N-Ncf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461468	M	MP:0008725	increased heart atrium size	Ncf1<em1(IMPC)Mbp>/Ncf1<em1(IMPC)Mbp>	C57BL/6N-Ncf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461468	M	MP:0002135	abnormal kidney morphology	Ncf1<em1(IMPC)Mbp>/Ncf1<em1(IMPC)Mbp>	C57BL/6N-Ncf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461468	M	MP:0002989	small kidney	Ncf1<em1(IMPC)Mbp>/Ncf1<em1(IMPC)Mbp>	C57BL/6N-Ncf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461472	F	MP:0002699	abnormal vitreous body morphology	Nell1<em1(IMPC)Mbp>/Nell1<em1(IMPC)Mbp>	C57BL/6N-Nell1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461472	F	MP:0001325	abnormal retina morphology	Nell1<em1(IMPC)Mbp>/Nell1<em1(IMPC)Mbp>	C57BL/6N-Nell1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461472	F	MP:0005562	decreased mean corpuscular hemoglobin	Nell1<em1(IMPC)Mbp>/Nell1<em1(IMPC)Mbp>	C57BL/6N-Nell1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461472	F	MP:0002989	small kidney	Nell1<em1(IMPC)Mbp>/Nell1<em1(IMPC)Mbp>	C57BL/6N-Nell1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461473	F	MP:0001417	decreased exploration in new environment	Nemp2<em1(IMPC)Tcp>/Nemp2<em1(IMPC)Tcp>	C57BL/6N-Nemp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461473	M	MP:0000689	abnormal spleen morphology	Nemp2<em1(IMPC)Tcp>/Nemp2<em1(IMPC)Tcp>	C57BL/6N-Nemp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461473	M	MP:0002060	abnormal skin morphology	Nemp2<em1(IMPC)Tcp>/Nemp2<em1(IMPC)Tcp>	C57BL/6N-Nemp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461474	M	MP:0000274	enlarged heart	Nhlrc3<em1(IMPC)Mbp>/Nhlrc3<em1(IMPC)Mbp>	C57BL/6N-Nhlrc3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461474	M	MP:0000266	abnormal heart morphology	Nhlrc3<em1(IMPC)Mbp>/Nhlrc3<em1(IMPC)Mbp>	C57BL/6N-Nhlrc3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461474	F	MP:0020421	increased freezing behavior	Nhlrc3<em1(IMPC)Mbp>/Nhlrc3<em1(IMPC)Mbp>	C57BL/6N-Nhlrc3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461475	F	MP:0000703	abnormal thymus morphology	Niban3<em1(IMPC)Mbp>/Niban3<em1(IMPC)Mbp>	C57BL/6N-Niban3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461475	F	MP:0000639	abnormal adrenal gland morphology	Niban3<em1(IMPC)Mbp>/Niban3<em1(IMPC)Mbp>	C57BL/6N-Niban3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461475	F	MP:0002092	abnormal eye morphology	Niban3<em1(IMPC)Mbp>/Niban3<em1(IMPC)Mbp>	C57BL/6N-Niban3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461475	M	MP:0002060	abnormal skin morphology	Niban3<em1(IMPC)Mbp>/Niban3<em1(IMPC)Mbp>	C57BL/6N-Niban3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461475	F	MP:0000709	enlarged thymus	Niban3<em1(IMPC)Mbp>/Niban3<em1(IMPC)Mbp>	C57BL/6N-Niban3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461477	F	MP:0002339	abnormal lymph node morphology	Nmnat2<em1(IMPC)Mbp>/Nmnat2<+>	C57BL/6N-Nmnat2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461477	F	MP:0000702	enlarged lymph nodes	Nmnat2<em1(IMPC)Mbp>/Nmnat2<+>	C57BL/6N-Nmnat2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461478	F	MP:0005576	decreased pulmonary ventilation	Nmral1<tm1.1(KOMP)Vlcg>/Nmral1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nmral1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461479	F	MP:0002989	small kidney	Nog<em1(IMPC)Mbp>/Nog<+>	C57BL/6N-Nog<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461479	F	MP:0003795	abnormal bone structure	Nog<em1(IMPC)Mbp>/Nog<+>	C57BL/6N-Nog<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461479	M	MP:0000443	abnormal snout morphology	Nog<em1(IMPC)Mbp>/Nog<+>	C57BL/6N-Nog<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461479	F	MP:0002135	abnormal kidney morphology	Nog<em1(IMPC)Mbp>/Nog<+>	C57BL/6N-Nog<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461479	F	MP:0002968	increased circulating alkaline phosphatase level	Nog<em1(IMPC)Mbp>/Nog<+>	C57BL/6N-Nog<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461480	M	MP:0002075	abnormal coat/hair pigmentation	Nol9<em1(IMPC)J>/Nol9<+>	C57BL/6NJ-Nol9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461480	F	MP:0005566	decreased blood urea nitrogen level	Nol9<em1(IMPC)J>/Nol9<+>	C57BL/6NJ-Nol9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461480	F	MP:0005553	increased circulating creatinine level	Nol9<em1(IMPC)J>/Nol9<+>	C57BL/6NJ-Nol9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461481	M	MP:0002968	increased circulating alkaline phosphatase level	Nop10<tm1.1(KOMP)Vlcg>/Nop10<+>	C57BL/6N-Nop10<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461482	F	MP:0000702	enlarged lymph nodes	Npas2<em1(IMPC)Mbp>/Npas2<em1(IMPC)Mbp>	C57BL/6N-Npas2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461482	M	MP:0011110	preweaning lethality, incomplete penetrance	Npas2<em1(IMPC)Mbp>/Npas2<em1(IMPC)Mbp>	C57BL/6N-Npas2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461482	F	MP:0001333	absent optic nerve	Npas2<em1(IMPC)Mbp>/Npas2<em1(IMPC)Mbp>	C57BL/6N-Npas2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461482	M	MP:0000219	increased neutrophil cell number	Npas2<em1(IMPC)Mbp>/Npas2<em1(IMPC)Mbp>	C57BL/6N-Npas2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461482	M	MP:0005016	decreased lymphocyte cell number	Npas2<em1(IMPC)Mbp>/Npas2<em1(IMPC)Mbp>	C57BL/6N-Npas2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461482	F	MP:0002339	abnormal lymph node morphology	Npas2<em1(IMPC)Mbp>/Npas2<em1(IMPC)Mbp>	C57BL/6N-Npas2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461483	M	MP:0002111	abnormal tail morphology	Npr2<em1(IMPC)H>/Npr2<+>	C57BL/6N-Npr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461483	M	MP:0000443	abnormal snout morphology	Npr2<em1(IMPC)H>/Npr2<+>	C57BL/6N-Npr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461484	F	MP:0009456	impaired cued conditioning behavior	Npr2<em1(IMPC)H>/Npr2<em1(IMPC)H>	C57BL/6N-Npr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461484	F	MP:0000745	tremors	Npr2<em1(IMPC)H>/Npr2<em1(IMPC)H>	C57BL/6N-Npr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461484	F	MP:0000432	abnormal head morphology	Npr2<em1(IMPC)H>/Npr2<em1(IMPC)H>	C57BL/6N-Npr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461484	F	MP:0020421	increased freezing behavior	Npr2<em1(IMPC)H>/Npr2<em1(IMPC)H>	C57BL/6N-Npr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461484	F	MP:0001406	abnormal gait	Npr2<em1(IMPC)H>/Npr2<em1(IMPC)H>	C57BL/6N-Npr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461484	F	MP:0002966	decreased circulating alkaline phosphatase level	Npr2<em1(IMPC)H>/Npr2<em1(IMPC)H>	C57BL/6N-Npr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461484	F	MP:0000443	abnormal snout morphology	Npr2<em1(IMPC)H>/Npr2<em1(IMPC)H>	C57BL/6N-Npr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461484	F	MP:0001392	abnormal locomotor behavior	Npr2<em1(IMPC)H>/Npr2<em1(IMPC)H>	C57BL/6N-Npr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461484	F	MP:0011496	abnormal head size	Npr2<em1(IMPC)H>/Npr2<em1(IMPC)H>	C57BL/6N-Npr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461484	F	MP:0001513	limb grasping	Npr2<em1(IMPC)H>/Npr2<em1(IMPC)H>	C57BL/6N-Npr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461484	F	MP:0001512	trunk curl	Npr2<em1(IMPC)H>/Npr2<em1(IMPC)H>	C57BL/6N-Npr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461485	M	MP:0000691	enlarged spleen	Npy2r<em1(IMPC)H>/Npy2r<em1(IMPC)H>	C57BL/6N-Npy2r<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461485	M	MP:0004952	increased spleen weight	Npy2r<em1(IMPC)H>/Npy2r<em1(IMPC)H>	C57BL/6N-Npy2r<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461487	F	MP:0005293	impaired glucose tolerance	Nt5c1b<tm1b(KOMP)Wtsi>/Nt5c1b<tm1b(KOMP)Wtsi>	C57BL/6N-Nt5c1b<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461487	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Nt5c1b<tm1b(KOMP)Wtsi>/Nt5c1b<tm1b(KOMP)Wtsi>	C57BL/6N-Nt5c1b<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461488	M	MP:0002135	abnormal kidney morphology	Nt5c2<em1(IMPC)Hmgu>/Nt5c2<em1(IMPC)Hmgu>	C57BL/6N-Nt5c2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461488	M	MP:0001489	decreased startle reflex	Nt5c2<em1(IMPC)Hmgu>/Nt5c2<em1(IMPC)Hmgu>	C57BL/6N-Nt5c2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461488	M	MP:0000598	abnormal liver morphology	Nt5c2<em1(IMPC)Hmgu>/Nt5c2<em1(IMPC)Hmgu>	C57BL/6N-Nt5c2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461489	F	MP:0011959	abnormal eye posterior chamber depth	Nudt5<tm1b(EUCOMM)Hmgu>/Nudt5<tm1b(EUCOMM)Hmgu>	C57BL/6N-Nudt5<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6461491	F	MP:0000702	enlarged lymph nodes	Nup155<em1(IMPC)Mbp>/Nup155<+>	C57BL/6N-Nup155<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461491	F	MP:0000689	abnormal spleen morphology	Nup155<em1(IMPC)Mbp>/Nup155<+>	C57BL/6N-Nup155<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461491	F	MP:0002339	abnormal lymph node morphology	Nup155<em1(IMPC)Mbp>/Nup155<+>	C57BL/6N-Nup155<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461491	F	MP:0005565	increased blood urea nitrogen level	Nup155<em1(IMPC)Mbp>/Nup155<+>	C57BL/6N-Nup155<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461491	F	MP:0000691	enlarged spleen	Nup155<em1(IMPC)Mbp>/Nup155<+>	C57BL/6N-Nup155<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461492	M	MP:0001556	increased circulating HDL cholesterol level	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6461492	M	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6461492	M	MP:0001552	increased circulating triglyceride level	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6461492	M	MP:0000627	abnormal mammary gland morphology	Nxn<tm1b(EUCOMM)Wtsi>/Nxn<+>	C57BL/6N-Nxn<tm1b(EUCOMM)Wtsi>/Ccpcz	N	MGI:5576271
MGI:6461494	M	MP:0011110	preweaning lethality, incomplete penetrance	Oasl1<tm1b(EUCOMM)Hmgu>/Oasl1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Oasl1<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6461495	F	MP:0009084	blind uterus	Odf2l<em1(IMPC)Mbp>/Odf2l<em1(IMPC)Mbp>	C57BL/6N-Odf2l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461495	F	MP:0002989	small kidney	Odf2l<em1(IMPC)Mbp>/Odf2l<em1(IMPC)Mbp>	C57BL/6N-Odf2l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461495	F	MP:0002135	abnormal kidney morphology	Odf2l<em1(IMPC)Mbp>/Odf2l<em1(IMPC)Mbp>	C57BL/6N-Odf2l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461497	M	MP:0002092	abnormal eye morphology	Or1e21<em1(IMPC)Mbp>/Or1e21<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e21<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461497	M	MP:0001175	abnormal lung morphology	Or1e21<em1(IMPC)Mbp>/Or1e21<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e21<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461497	M	MP:0001146	abnormal testis morphology	Or1e21<em1(IMPC)Mbp>/Or1e21<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e21<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461497	M	MP:0001147	small testis	Or1e21<em1(IMPC)Mbp>/Or1e21<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e21<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461497	F	MP:0009709	hydrometra	Or1e21<em1(IMPC)Mbp>/Or1e21<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e21<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461497	M	MP:0000538	abnormal urinary bladder morphology	Or1e21<em1(IMPC)Mbp>/Or1e21<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e21<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461497	F	MP:0001120	abnormal uterus morphology	Or1e21<em1(IMPC)Mbp>/Or1e21<em1(IMPC)Mbp>	C57BL/6NCrl-Or1e21<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461499	F	MP:0000198	decreased circulating phosphate level	Olig1<em2(IMPC)Ics>/Olig1<em2(IMPC)Ics>	C57BL/6N-Olig1<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461499	M	MP:0001399	hyperactivity	Olig1<em2(IMPC)Ics>/Olig1<em2(IMPC)Ics>	C57BL/6N-Olig1<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461501	M	MP:0009142	decreased prepulse inhibition	Oser1<em1(IMPC)Bay>/Oser1<+>	C57BL/6N-Oser1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461503	F	MP:0008810	increased circulating iron level	Otp<tm1b(EUCOMM)Wtsi>/Otp<+>	C57BL/6N-Otp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6461504	M	MP:0010124	decreased bone mineral content	Otub1<tm1b(EUCOMM)Hmgu>/Otub1<+>	C57BL/6N-Otub1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461505	M	MP:0010579	increased heart left ventricle size	Oxa1l<em1(IMPC)Bay>/Oxa1l<+>	C57BL/6N-Oxa1l<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6461506	M	MP:0003179	thrombocytopenia	Oxr1<tm1a(EUCOMM)Wtsi>/Oxr1<+>	C57BL/6N-Oxr1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461506	F	MP:0001258	decreased body length	Oxr1<tm1a(EUCOMM)Wtsi>/Oxr1<+>	C57BL/6N-Oxr1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461508	M	MP:0003068	enlarged kidney	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	M	MP:0000601	small liver	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	M	MP:0001552	increased circulating triglyceride level	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	F	MP:0002060	abnormal skin morphology	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	M	MP:0000599	enlarged liver	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	M	MP:0000702	enlarged lymph nodes	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	M	MP:0005344	increased circulating bilirubin level	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	F	MP:0002188	small heart	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	M	MP:0002339	abnormal lymph node morphology	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	M	MP:0000598	abnormal liver morphology	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	M	MP:0005561	increased mean corpuscular hemoglobin	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	M	MP:0002590	increased mean corpuscular volume	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	F	MP:0002989	small kidney	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	M	MP:0005179	decreased circulating cholesterol level	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	F	MP:0001120	abnormal uterus morphology	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461508	M	MP:0000274	enlarged heart	Padi4<em1(IMPC)Mbp>/Padi4<em1(IMPC)Mbp>	C57BL/6N-Padi4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461509	M	MP:0010053	decreased grip strength	Palmd<em1(IMPC)J>/Palmd<em1(IMPC)J>	C57BL/6NJ-Palmd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461510	F	MP:0010088	decreased circulating fructosamine level	Pam<em1(IMPC)Hmgu>/Pam<+>	C57BL/6N-Pam<em1(IMPC)Hmgu>/H	N	MGI:5576271
MGI:6461511	F	MP:0005344	increased circulating bilirubin level	Parp11<tm1.1(KOMP)Vlcg>/Parp11<tm1.1(KOMP)Vlcg>	C57BL/6N-Parp11<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6461512	M	MP:0005576	decreased pulmonary ventilation	Parp12<tm1.1(KOMP)Vlcg>/Parp12<tm1.1(KOMP)Vlcg>	C57BL/6N-Parp12<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461512	M	MP:0005573	increased pulmonary respiratory rate	Parp12<tm1.1(KOMP)Vlcg>/Parp12<tm1.1(KOMP)Vlcg>	C57BL/6N-Parp12<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461514	F	MP:0001120	abnormal uterus morphology	Paxx<em1(IMPC)Mbp>/Paxx<em1(IMPC)Mbp>	C57BL/6NCrl-Paxx<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461514	F	MP:0000702	enlarged lymph nodes	Paxx<em1(IMPC)Mbp>/Paxx<em1(IMPC)Mbp>	C57BL/6NCrl-Paxx<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461514	M	MP:0020421	increased freezing behavior	Paxx<em1(IMPC)Mbp>/Paxx<em1(IMPC)Mbp>	C57BL/6NCrl-Paxx<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461514	F	MP:0002339	abnormal lymph node morphology	Paxx<em1(IMPC)Mbp>/Paxx<em1(IMPC)Mbp>	C57BL/6NCrl-Paxx<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461515	F	MP:0008528	polycystic kidney	Pccb<tm1.1(KOMP)Vlcg>/Pccb<+>	C57BL/6N-Pccb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6461515	F	MP:0002135	abnormal kidney morphology	Pccb<tm1.1(KOMP)Vlcg>/Pccb<+>	C57BL/6N-Pccb<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6461516	M	MP:0000470	abnormal stomach morphology	Pck2<em1(IMPC)Tcp>/Pck2<em1(IMPC)Tcp>	C57BL/6N-Pck2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461516	M	MP:0002644	decreased circulating triglyceride level	Pck2<em1(IMPC)Tcp>/Pck2<em1(IMPC)Tcp>	C57BL/6N-Pck2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461516	M	MP:0000702	enlarged lymph nodes	Pck2<em1(IMPC)Tcp>/Pck2<em1(IMPC)Tcp>	C57BL/6N-Pck2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461516	M	MP:0002060	abnormal skin morphology	Pck2<em1(IMPC)Tcp>/Pck2<em1(IMPC)Tcp>	C57BL/6N-Pck2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461516	M	MP:0004930	small epididymis	Pck2<em1(IMPC)Tcp>/Pck2<em1(IMPC)Tcp>	C57BL/6N-Pck2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461518	M	MP:0005564	increased hemoglobin content	Pdgfrl<em1(IMPC)J>/Pdgfrl<em1(IMPC)J>	C57BL/6NJ-Pdgfrl<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461519	M	MP:0000702	enlarged lymph nodes	Pdk2<em1(IMPC)Mbp>/Pdk2<em1(IMPC)Mbp>	C57BL/6N-Pdk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461519	M	MP:0002339	abnormal lymph node morphology	Pdk2<em1(IMPC)Mbp>/Pdk2<em1(IMPC)Mbp>	C57BL/6N-Pdk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461519	F	MP:0002152	abnormal brain morphology	Pdk2<em1(IMPC)Mbp>/Pdk2<em1(IMPC)Mbp>	C57BL/6N-Pdk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461519	M	MP:0003068	enlarged kidney	Pdk2<em1(IMPC)Mbp>/Pdk2<em1(IMPC)Mbp>	C57BL/6N-Pdk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461519	F	MP:0001297	microphthalmia	Pdk2<em1(IMPC)Mbp>/Pdk2<em1(IMPC)Mbp>	C57BL/6N-Pdk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461519	M	MP:0000598	abnormal liver morphology	Pdk2<em1(IMPC)Mbp>/Pdk2<em1(IMPC)Mbp>	C57BL/6N-Pdk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461519	M	MP:0001148	enlarged testis	Pdk2<em1(IMPC)Mbp>/Pdk2<em1(IMPC)Mbp>	C57BL/6N-Pdk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461519	F	MP:0001120	abnormal uterus morphology	Pdk2<em1(IMPC)Mbp>/Pdk2<em1(IMPC)Mbp>	C57BL/6N-Pdk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461519	M	MP:0001146	abnormal testis morphology	Pdk2<em1(IMPC)Mbp>/Pdk2<em1(IMPC)Mbp>	C57BL/6N-Pdk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461519	F	MP:0002060	abnormal skin morphology	Pdk2<em1(IMPC)Mbp>/Pdk2<em1(IMPC)Mbp>	C57BL/6N-Pdk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461519	M	MP:0002135	abnormal kidney morphology	Pdk2<em1(IMPC)Mbp>/Pdk2<em1(IMPC)Mbp>	C57BL/6N-Pdk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461520	M	MP:0002060	abnormal skin morphology	Pdlim7<em1(IMPC)Mbp>/Pdlim7<em1(IMPC)Mbp>	C57BL/6N-Pdlim7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461520	F	MP:0000601	small liver	Pdlim7<em1(IMPC)Mbp>/Pdlim7<em1(IMPC)Mbp>	C57BL/6N-Pdlim7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461520	F	MP:0000598	abnormal liver morphology	Pdlim7<em1(IMPC)Mbp>/Pdlim7<em1(IMPC)Mbp>	C57BL/6N-Pdlim7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461520	F	MP:0000689	abnormal spleen morphology	Pdlim7<em1(IMPC)Mbp>/Pdlim7<em1(IMPC)Mbp>	C57BL/6N-Pdlim7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461520	F	MP:0002339	abnormal lymph node morphology	Pdlim7<em1(IMPC)Mbp>/Pdlim7<em1(IMPC)Mbp>	C57BL/6N-Pdlim7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461520	M	MP:0000274	enlarged heart	Pdlim7<em1(IMPC)Mbp>/Pdlim7<em1(IMPC)Mbp>	C57BL/6N-Pdlim7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461520	F	MP:0002599	increased mean platelet volume	Pdlim7<em1(IMPC)Mbp>/Pdlim7<em1(IMPC)Mbp>	C57BL/6N-Pdlim7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461520	M	MP:0002699	abnormal vitreous body morphology	Pdlim7<em1(IMPC)Mbp>/Pdlim7<em1(IMPC)Mbp>	C57BL/6N-Pdlim7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461520	F	MP:0000691	enlarged spleen	Pdlim7<em1(IMPC)Mbp>/Pdlim7<em1(IMPC)Mbp>	C57BL/6N-Pdlim7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461520	F	MP:0000702	enlarged lymph nodes	Pdlim7<em1(IMPC)Mbp>/Pdlim7<em1(IMPC)Mbp>	C57BL/6N-Pdlim7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461520	M	MP:0001304	cataract	Pdlim7<em1(IMPC)Mbp>/Pdlim7<em1(IMPC)Mbp>	C57BL/6N-Pdlim7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461521	F	MP:0001258	decreased body length	Pebp4<tm1b(EUCOMM)Hmgu>/Pebp4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Pebp4<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6461523	M	MP:0001417	decreased exploration in new environment	Pfdn1<em1(IMPC)J>/Pfdn1<+>	C57BL/6NJ-Pfdn1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461523	M	MP:0001513	limb grasping	Pfdn1<em1(IMPC)J>/Pfdn1<+>	C57BL/6NJ-Pfdn1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461523	M	MP:0001392	abnormal locomotor behavior	Pfdn1<em1(IMPC)J>/Pfdn1<+>	C57BL/6NJ-Pfdn1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461524	M	MP:0012125	decreased bronchoconstrictive response	Pfn4<tm1b(KOMP)Wtsi>/Pfn4<tm1b(KOMP)Wtsi>	C57BL/6N-Pfn4<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6461524	F	MP:0005573	increased pulmonary respiratory rate	Pfn4<tm1b(KOMP)Wtsi>/Pfn4<tm1b(KOMP)Wtsi>	C57BL/6N-Pfn4<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6461525	M	MP:0002152	abnormal brain morphology	Phf20l1<em1(IMPC)Tcp>/Phf20l1<em1(IMPC)Tcp>	C57BL/6N-Phf20l1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461525	M	MP:0002833	increased heart weight	Phf20l1<em1(IMPC)Tcp>/Phf20l1<em1(IMPC)Tcp>	C57BL/6N-Phf20l1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461525	M	MP:0004952	increased spleen weight	Phf20l1<em1(IMPC)Tcp>/Phf20l1<em1(IMPC)Tcp>	C57BL/6N-Phf20l1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461525	F	MP:0005561	increased mean corpuscular hemoglobin	Phf20l1<em1(IMPC)Tcp>/Phf20l1<em1(IMPC)Tcp>	C57BL/6N-Phf20l1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461525	M	MP:0000702	enlarged lymph nodes	Phf20l1<em1(IMPC)Tcp>/Phf20l1<em1(IMPC)Tcp>	C57BL/6N-Phf20l1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461525	M	MP:0003960	increased lean body mass	Phf20l1<em1(IMPC)Tcp>/Phf20l1<em1(IMPC)Tcp>	C57BL/6N-Phf20l1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461525	M	MP:0010025	decreased total body fat amount	Phf20l1<em1(IMPC)Tcp>/Phf20l1<em1(IMPC)Tcp>	C57BL/6N-Phf20l1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461525	M	MP:0000157	abnormal sternum morphology	Phf20l1<em1(IMPC)Tcp>/Phf20l1<em1(IMPC)Tcp>	C57BL/6N-Phf20l1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461525	M	MP:0005016	decreased lymphocyte cell number	Phf20l1<em1(IMPC)Tcp>/Phf20l1<em1(IMPC)Tcp>	C57BL/6N-Phf20l1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461527	F	MP:0000220	increased monocyte cell number	Pi4ka<tm1b(EUCOMM)Wtsi>/Pi4ka<+>	C57BL/6N-Pi4ka<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6461527	F	MP:0002608	increased hematocrit	Pi4ka<tm1b(EUCOMM)Wtsi>/Pi4ka<+>	C57BL/6N-Pi4ka<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6461527	F	MP:0001513	limb grasping	Pi4ka<tm1b(EUCOMM)Wtsi>/Pi4ka<+>	C57BL/6N-Pi4ka<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6461528	M	MP:0002574	increased vertical activity	Piezo2<em2(IMPC)J>/Piezo2<+>	C57BL/6NJ-Piezo2<em2(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461528	M	MP:0001552	increased circulating triglyceride level	Piezo2<em2(IMPC)J>/Piezo2<+>	C57BL/6NJ-Piezo2<em2(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461529	M	MP:0001415	increased exploration in new environment	Pigk<em1(IMPC)Bay>/Pigk<+>	C57BL/6N-Pigk<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461530	F	MP:0002135	abnormal kidney morphology	Pigm<tm1.1(KOMP)Vlcg>/Pigm<+>	C57BL/6N-Pigm<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461533	F	MP:0000601	small liver	Pkdcc<em1(IMPC)Mbp>/Pkdcc<+>	C57BL/6N-Pkdcc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461533	F	MP:0000598	abnormal liver morphology	Pkdcc<em1(IMPC)Mbp>/Pkdcc<+>	C57BL/6N-Pkdcc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461533	F	MP:0002989	small kidney	Pkdcc<em1(IMPC)Mbp>/Pkdcc<+>	C57BL/6N-Pkdcc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461533	F	MP:0002135	abnormal kidney morphology	Pkdcc<em1(IMPC)Mbp>/Pkdcc<+>	C57BL/6N-Pkdcc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461534	M	MP:0005011	increased eosinophil cell number	Plaat5<em1(IMPC)Tcp>/Plaat5<em1(IMPC)Tcp>	C57BL/6N-Plaat5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461534	F	MP:0001417	decreased exploration in new environment	Plaat5<em1(IMPC)Tcp>/Plaat5<em1(IMPC)Tcp>	C57BL/6N-Plaat5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461534	F	MP:0009453	enhanced contextual conditioning behavior	Plaat5<em1(IMPC)Tcp>/Plaat5<em1(IMPC)Tcp>	C57BL/6N-Plaat5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461535	M	MP:0001925	male infertility	Plcb1<em1(IMPC)Mbp>/Plcb1<em1(IMPC)Mbp>	C57BL/6N-Plcb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461535	F	MP:0001926	female infertility	Plcb1<em1(IMPC)Mbp>/Plcb1<em1(IMPC)Mbp>	C57BL/6N-Plcb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461536	F	MP:0005576	decreased pulmonary ventilation	Plcb2<tm1b(KOMP)Wtsi>/Plcb2<tm1b(KOMP)Wtsi>	C57BL/6N-Plcb2<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6461537	M	MP:0002060	abnormal skin morphology	Plek2<em1(IMPC)Tcp>/Plek2<em1(IMPC)Tcp>	C57BL/6N-Plek2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461537	M	MP:0000157	abnormal sternum morphology	Plek2<em1(IMPC)Tcp>/Plek2<em1(IMPC)Tcp>	C57BL/6N-Plek2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461541	F	MP:0011965	decreased total retina thickness	Plscr1<tm1b(EUCOMM)Hmgu>/Plscr1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plscr1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461541	F	MP:0003731	abnormal retina outer nuclear layer morphology	Plscr1<tm1b(EUCOMM)Hmgu>/Plscr1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plscr1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461541	F	MP:0001488	increased startle reflex	Plscr1<tm1b(EUCOMM)Hmgu>/Plscr1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plscr1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461541	F	MP:0010393	shortened QRS complex duration	Plscr1<tm1b(EUCOMM)Hmgu>/Plscr1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Plscr1<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6461542	F	MP:0002989	small kidney	Plxnc1<em1(IMPC)Mbp>/Plxnc1<em1(IMPC)Mbp>	C57BL/6N-Plxnc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461542	M	MP:0000692	small spleen	Plxnc1<em1(IMPC)Mbp>/Plxnc1<em1(IMPC)Mbp>	C57BL/6N-Plxnc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461542	F	MP:0001556	increased circulating HDL cholesterol level	Plxnc1<em1(IMPC)Mbp>/Plxnc1<em1(IMPC)Mbp>	C57BL/6N-Plxnc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461542	F	MP:0000194	increased circulating calcium level	Plxnc1<em1(IMPC)Mbp>/Plxnc1<em1(IMPC)Mbp>	C57BL/6N-Plxnc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461542	M	MP:0000689	abnormal spleen morphology	Plxnc1<em1(IMPC)Mbp>/Plxnc1<em1(IMPC)Mbp>	C57BL/6N-Plxnc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461542	M	MP:0003068	enlarged kidney	Plxnc1<em1(IMPC)Mbp>/Plxnc1<em1(IMPC)Mbp>	C57BL/6N-Plxnc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461543	F	MP:0000194	increased circulating calcium level	Pmpca<em1(IMPC)J>/Pmpca<+>	C57BL/6NJ-Pmpca<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461543	F	MP:0001284	absent vibrissae	Pmpca<em1(IMPC)J>/Pmpca<+>	C57BL/6NJ-Pmpca<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461544	F	MP:0000689	abnormal spleen morphology	Pnpla5<em1(IMPC)Mbp>/Pnpla5<em1(IMPC)Mbp>	C57BL/6N-Pnpla5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461544	F	MP:0000691	enlarged spleen	Pnpla5<em1(IMPC)Mbp>/Pnpla5<em1(IMPC)Mbp>	C57BL/6N-Pnpla5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461547	M	MP:0011874	enlarged urinary bladder	Polr1b<em1(IMPC)Tcp>/Polr1b<+>	C57BL/6NCrl-Polr1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461547	M	MP:0001200	thick skin	Polr1b<em1(IMPC)Tcp>/Polr1b<+>	C57BL/6NCrl-Polr1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461547	M	MP:0000702	enlarged lymph nodes	Polr1b<em1(IMPC)Tcp>/Polr1b<+>	C57BL/6NCrl-Polr1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461547	M	MP:0003068	enlarged kidney	Polr1b<em1(IMPC)Tcp>/Polr1b<+>	C57BL/6NCrl-Polr1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461547	M	MP:0000598	abnormal liver morphology	Polr1b<em1(IMPC)Tcp>/Polr1b<+>	C57BL/6NCrl-Polr1b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461549	M	MP:0011874	enlarged urinary bladder	Polr3d<em1(IMPC)Tcp>/Polr3d<+>	C57BL/6N-Polr3d<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461549	F	MP:0008935	decreased mean platelet volume	Polr3d<em1(IMPC)Tcp>/Polr3d<+>	C57BL/6N-Polr3d<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461549	F	MP:0005278	abnormal cholesterol homeostasis	Polr3d<em1(IMPC)Tcp>/Polr3d<+>	C57BL/6N-Polr3d<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461549	F	MP:0002966	decreased circulating alkaline phosphatase level	Polr3d<em1(IMPC)Tcp>/Polr3d<+>	C57BL/6N-Polr3d<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461553	M	MP:0002989	small kidney	Ppil1<em1(IMPC)Mbp>/Ppil1<+>	C57BL/6N-Ppil1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461553	M	MP:0002135	abnormal kidney morphology	Ppil1<em1(IMPC)Mbp>/Ppil1<+>	C57BL/6N-Ppil1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461553	M	MP:0002060	abnormal skin morphology	Ppil1<em1(IMPC)Mbp>/Ppil1<+>	C57BL/6N-Ppil1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461553	F	MP:0000692	small spleen	Ppil1<em1(IMPC)Mbp>/Ppil1<+>	C57BL/6N-Ppil1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461553	F	MP:0008528	polycystic kidney	Ppil1<em1(IMPC)Mbp>/Ppil1<+>	C57BL/6N-Ppil1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461556	F	MP:0002339	abnormal lymph node morphology	Ppp2r2d<em1(IMPC)Mbp>/Ppp2r2d<em1(IMPC)Mbp>	C57BL/6N-Ppp2r2d<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461556	F	MP:0000702	enlarged lymph nodes	Ppp2r2d<em1(IMPC)Mbp>/Ppp2r2d<em1(IMPC)Mbp>	C57BL/6N-Ppp2r2d<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461557	F	MP:0005565	increased blood urea nitrogen level	Ppt2<tm2b(KOMP)Wtsi>/Ppt2<tm2b(KOMP)Wtsi>	C57BL/6N-Ppt2<tm2b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6461558	M	MP:0000280	thin ventricular wall	Prex2<em1(IMPC)Bay>/Prex2<em1(IMPC)Bay>	C57BL/6N-Prex2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461559	M	MP:0001417	decreased exploration in new environment	Prg4<em1(IMPC)Ccpcz>/Prg4<em1(IMPC)Ccpcz>	C57BL/6N-Prg4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461559	F	MP:0001262	decreased body weight	Prg4<em1(IMPC)Ccpcz>/Prg4<em1(IMPC)Ccpcz>	C57BL/6N-Prg4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461559	F	MP:0002060	abnormal skin morphology	Prg4<em1(IMPC)Ccpcz>/Prg4<em1(IMPC)Ccpcz>	C57BL/6N-Prg4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461559	F	MP:0002932	abnormal joint morphology	Prg4<em1(IMPC)Ccpcz>/Prg4<em1(IMPC)Ccpcz>	C57BL/6N-Prg4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461560	M	MP:0002941	increased circulating alanine transaminase level	Prkacb<em1(IMPC)H>/Prkacb<+>	C57BL/6NTac-Prkacb<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461561	F	MP:0013279	increased fasting circulating glucose level	Prpf4b<em1(IMPC)J>/Prpf4b<+>	C57BL/6NJ-Prpf4b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461563	M	MP:0010067	increased red blood cell distribution width	Prxl2b<tm1b(EUCOMM)Hmgu>/Prxl2b<tm1b(EUCOMM)Hmgu>	C57BL/6N-Prxl2b<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6461564	F	MP:0010053	decreased grip strength	Psd4<tm1.1(KOMP)Vlcg>/Psd4<tm1.1(KOMP)Vlcg>	C57BL/6N-Psd4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461565	M	MP:0000692	small spleen	Psd<em1(IMPC)Mbp>/Psd<em1(IMPC)Mbp>	C57BL/6NCrl-Psd<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461565	F	MP:0002092	abnormal eye morphology	Psd<em1(IMPC)Mbp>/Psd<em1(IMPC)Mbp>	C57BL/6NCrl-Psd<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461565	M	MP:0000689	abnormal spleen morphology	Psd<em1(IMPC)Mbp>/Psd<em1(IMPC)Mbp>	C57BL/6NCrl-Psd<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461566	M	MP:0001925	male infertility	Psma8<em1(IMPC)Tcp>/Psma8<em1(IMPC)Tcp>	C57BL/6N-Psma8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461566	M	MP:0011874	enlarged urinary bladder	Psma8<em1(IMPC)Tcp>/Psma8<em1(IMPC)Tcp>	C57BL/6N-Psma8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461566	M	MP:0003068	enlarged kidney	Psma8<em1(IMPC)Tcp>/Psma8<em1(IMPC)Tcp>	C57BL/6N-Psma8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461566	M	MP:0000706	small thymus	Psma8<em1(IMPC)Tcp>/Psma8<em1(IMPC)Tcp>	C57BL/6N-Psma8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461566	M	MP:0001944	abnormal pancreas morphology	Psma8<em1(IMPC)Tcp>/Psma8<em1(IMPC)Tcp>	C57BL/6N-Psma8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461566	M	MP:0002059	abnormal seminal vesicle morphology	Psma8<em1(IMPC)Tcp>/Psma8<em1(IMPC)Tcp>	C57BL/6N-Psma8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461566	F	MP:0000220	increased monocyte cell number	Psma8<em1(IMPC)Tcp>/Psma8<em1(IMPC)Tcp>	C57BL/6N-Psma8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461566	M	MP:0002060	abnormal skin morphology	Psma8<em1(IMPC)Tcp>/Psma8<em1(IMPC)Tcp>	C57BL/6N-Psma8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461566	M	MP:0001147	small testis	Psma8<em1(IMPC)Tcp>/Psma8<em1(IMPC)Tcp>	C57BL/6N-Psma8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461566	M	MP:0004930	small epididymis	Psma8<em1(IMPC)Tcp>/Psma8<em1(IMPC)Tcp>	C57BL/6N-Psma8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461568	M	MP:0001925	male infertility	Pspc1<em1(IMPC)Mbp>/Pspc1<em1(IMPC)Mbp>	C57BL/6N-Pspc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461568	M	MP:0001488	increased startle reflex	Pspc1<em1(IMPC)Mbp>/Pspc1<em1(IMPC)Mbp>	C57BL/6N-Pspc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461568	M	MP:0000692	small spleen	Pspc1<em1(IMPC)Mbp>/Pspc1<em1(IMPC)Mbp>	C57BL/6N-Pspc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461568	F	MP:0000691	enlarged spleen	Pspc1<em1(IMPC)Mbp>/Pspc1<em1(IMPC)Mbp>	C57BL/6N-Pspc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461568	F	MP:0001417	decreased exploration in new environment	Pspc1<em1(IMPC)Mbp>/Pspc1<em1(IMPC)Mbp>	C57BL/6N-Pspc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461570	F	MP:0002152	abnormal brain morphology	Ptgis<em1(IMPC)Mbp>/Ptgis<em1(IMPC)Mbp>	C57BL/6N-Ptgis<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461570	F	MP:0000703	abnormal thymus morphology	Ptgis<em1(IMPC)Mbp>/Ptgis<em1(IMPC)Mbp>	C57BL/6N-Ptgis<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461570	F	MP:0010067	increased red blood cell distribution width	Ptgis<em1(IMPC)Mbp>/Ptgis<em1(IMPC)Mbp>	C57BL/6N-Ptgis<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461570	M	MP:0003918	decreased kidney weight	Ptgis<em1(IMPC)Mbp>/Ptgis<em1(IMPC)Mbp>	C57BL/6N-Ptgis<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461570	F	MP:0005238	increased brain size	Ptgis<em1(IMPC)Mbp>/Ptgis<em1(IMPC)Mbp>	C57BL/6N-Ptgis<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461570	F	MP:0000709	enlarged thymus	Ptgis<em1(IMPC)Mbp>/Ptgis<em1(IMPC)Mbp>	C57BL/6N-Ptgis<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461570	F	MP:0000689	abnormal spleen morphology	Ptgis<em1(IMPC)Mbp>/Ptgis<em1(IMPC)Mbp>	C57BL/6N-Ptgis<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461570	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Ptgis<em1(IMPC)Mbp>/Ptgis<em1(IMPC)Mbp>	C57BL/6N-Ptgis<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461570	M	MP:0008528	polycystic kidney	Ptgis<em1(IMPC)Mbp>/Ptgis<em1(IMPC)Mbp>	C57BL/6N-Ptgis<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461570	F	MP:0000691	enlarged spleen	Ptgis<em1(IMPC)Mbp>/Ptgis<em1(IMPC)Mbp>	C57BL/6N-Ptgis<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461570	M	MP:0000266	abnormal heart morphology	Ptgis<em1(IMPC)Mbp>/Ptgis<em1(IMPC)Mbp>	C57BL/6N-Ptgis<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461570	M	MP:0002591	decreased mean corpuscular volume	Ptgis<em1(IMPC)Mbp>/Ptgis<em1(IMPC)Mbp>	C57BL/6N-Ptgis<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461570	M	MP:0000274	enlarged heart	Ptgis<em1(IMPC)Mbp>/Ptgis<em1(IMPC)Mbp>	C57BL/6N-Ptgis<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461571	M	MP:0003961	decreased lean body mass	Ptgr1<tm1b(EUCOMM)Wtsi>/Ptgr1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ptgr1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6461571	M	MP:0010124	decreased bone mineral content	Ptgr1<tm1b(EUCOMM)Wtsi>/Ptgr1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ptgr1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6461571	M	MP:0010024	increased total body fat amount	Ptgr1<tm1b(EUCOMM)Wtsi>/Ptgr1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ptgr1<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6461572	M	MP:0002833	increased heart weight	Pth2r<tm2a(KOMP)Wtsi>/Pth2r<tm2a(KOMP)Wtsi>	C57BL/6N-Pth2r<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461573	F	MP:0000218	increased leukocyte cell number	Ptprd<tm2a(KOMP)Wtsi>/Ptprd<tm2a(KOMP)Wtsi>	C57BL/6N-Ptprd<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461573	F	MP:0008810	increased circulating iron level	Ptprd<tm2a(KOMP)Wtsi>/Ptprd<tm2a(KOMP)Wtsi>	C57BL/6N-Ptprd<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461573	F	MP:0010123	increased bone mineral content	Ptprd<tm2a(KOMP)Wtsi>/Ptprd<tm2a(KOMP)Wtsi>	C57BL/6N-Ptprd<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461574	F	MP:0001566	increased circulating phosphate level	Pus1<em1(IMPC)J>/Pus1<em1(IMPC)J>	C57BL/6NJ-Pus1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461574	F	MP:0010053	decreased grip strength	Pus1<em1(IMPC)J>/Pus1<em1(IMPC)J>	C57BL/6NJ-Pus1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461574	F	MP:0001402	decreased locomotor activity	Pus1<em1(IMPC)J>/Pus1<em1(IMPC)J>	C57BL/6NJ-Pus1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461574	F	MP:0002797	increased thigmotaxis	Pus1<em1(IMPC)J>/Pus1<em1(IMPC)J>	C57BL/6NJ-Pus1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461574	F	MP:0005344	increased circulating bilirubin level	Pus1<em1(IMPC)J>/Pus1<em1(IMPC)J>	C57BL/6NJ-Pus1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461574	F	MP:0001529	abnormal vocalization	Pus1<em1(IMPC)J>/Pus1<em1(IMPC)J>	C57BL/6NJ-Pus1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461575	M	MP:0005633	increased circulating sodium level	Rab20<tm1b(EUCOMM)Hmgu>/Rab20<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rab20<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461576	F	MP:0003795	abnormal bone structure	Rab28<em1(IMPC)J>/Rab28<em1(IMPC)J>	C57BL/6NJ-Rab28<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461576	F	MP:0000063	decreased bone mineral density	Rab28<em1(IMPC)J>/Rab28<em1(IMPC)J>	C57BL/6NJ-Rab28<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461576	F	MP:0005567	decreased circulating total protein level	Rab28<em1(IMPC)J>/Rab28<em1(IMPC)J>	C57BL/6NJ-Rab28<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461576	F	MP:0010024	increased total body fat amount	Rab28<em1(IMPC)J>/Rab28<em1(IMPC)J>	C57BL/6NJ-Rab28<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461576	F	MP:0001552	increased circulating triglyceride level	Rab28<em1(IMPC)J>/Rab28<em1(IMPC)J>	C57BL/6NJ-Rab28<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461576	F	MP:0003961	decreased lean body mass	Rab28<em1(IMPC)J>/Rab28<em1(IMPC)J>	C57BL/6NJ-Rab28<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461577	F	MP:0001392	abnormal locomotor behavior	Rab3gap1<em1(IMPC)J>/Rab3gap1<em1(IMPC)J>	C57BL/6NJ-Rab3gap1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461577	M	MP:0010052	increased grip strength	Rab3gap1<em1(IMPC)J>/Rab3gap1<em1(IMPC)J>	C57BL/6NJ-Rab3gap1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461577	F	MP:0001417	decreased exploration in new environment	Rab3gap1<em1(IMPC)J>/Rab3gap1<em1(IMPC)J>	C57BL/6NJ-Rab3gap1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461577	M	MP:0002968	increased circulating alkaline phosphatase level	Rab3gap1<em1(IMPC)J>/Rab3gap1<em1(IMPC)J>	C57BL/6NJ-Rab3gap1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461578	M	MP:0000266	abnormal heart morphology	Rac1<em1(IMPC)Mbp>/Rac1<+>	C57BL/6N-Rac1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461578	F	MP:0001297	microphthalmia	Rac1<em1(IMPC)Mbp>/Rac1<+>	C57BL/6N-Rac1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461578	F	MP:0001399	hyperactivity	Rac1<em1(IMPC)Mbp>/Rac1<+>	C57BL/6N-Rac1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461578	M	MP:0001146	abnormal testis morphology	Rac1<em1(IMPC)Mbp>/Rac1<+>	C57BL/6N-Rac1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461578	F	MP:0002092	abnormal eye morphology	Rac1<em1(IMPC)Mbp>/Rac1<+>	C57BL/6N-Rac1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461578	M	MP:0001147	small testis	Rac1<em1(IMPC)Mbp>/Rac1<+>	C57BL/6N-Rac1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461578	F	MP:0002968	increased circulating alkaline phosphatase level	Rac1<em1(IMPC)Mbp>/Rac1<+>	C57BL/6N-Rac1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461578	M	MP:0002989	small kidney	Rac1<em1(IMPC)Mbp>/Rac1<+>	C57BL/6N-Rac1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461578	M	MP:0002188	small heart	Rac1<em1(IMPC)Mbp>/Rac1<+>	C57BL/6N-Rac1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461578	M	MP:0005562	decreased mean corpuscular hemoglobin	Rac1<em1(IMPC)Mbp>/Rac1<+>	C57BL/6N-Rac1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461579	F	MP:0005560	decreased circulating glucose level	Rad51ap1<tm1.1(KOMP)Vlcg>/Rad51ap1<tm1.1(KOMP)Vlcg>	C57BL/6N-Rad51ap1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461580	M	MP:0001392	abnormal locomotor behavior	Ralgapa1<em1(IMPC)J>/Ralgapa1<+>	C57BL/6NJ-Ralgapa1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461580	M	MP:0001417	decreased exploration in new environment	Ralgapa1<em1(IMPC)J>/Ralgapa1<+>	C57BL/6NJ-Ralgapa1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461580	F	MP:0001399	hyperactivity	Ralgapa1<em1(IMPC)J>/Ralgapa1<+>	C57BL/6NJ-Ralgapa1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461580	F	MP:0001513	limb grasping	Ralgapa1<em1(IMPC)J>/Ralgapa1<+>	C57BL/6NJ-Ralgapa1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461581	F	MP:0005343	increased circulating aspartate transaminase level	Ralgps1<em1(IMPC)J>/Ralgps1<em1(IMPC)J>	C57BL/6NJ-Ralgps1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461582	M	MP:0002059	abnormal seminal vesicle morphology	Ranbp17<em1(IMPC)Tcp>/Ranbp17<em1(IMPC)Tcp>	C57BL/6N-Ranbp17<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461582	F	MP:0000470	abnormal stomach morphology	Ranbp17<em1(IMPC)Tcp>/Ranbp17<em1(IMPC)Tcp>	C57BL/6N-Ranbp17<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461582	F	MP:0000691	enlarged spleen	Ranbp17<em1(IMPC)Tcp>/Ranbp17<em1(IMPC)Tcp>	C57BL/6N-Ranbp17<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461582	F	MP:0001293	anophthalmia	Ranbp17<em1(IMPC)Tcp>/Ranbp17<em1(IMPC)Tcp>	C57BL/6N-Ranbp17<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461584	M	MP:0005344	increased circulating bilirubin level	Rapgef2<em1(IMPC)H>/Rapgef2<+>	C57BL/6N-Rapgef2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461585	F	MP:0003179	thrombocytopenia	Rapgef4<em1(IMPC)H>/Rapgef4<+>	C57BL/6NTac-Rapgef4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461585	F	MP:0010067	increased red blood cell distribution width	Rapgef4<em1(IMPC)H>/Rapgef4<+>	C57BL/6NTac-Rapgef4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461587	M	MP:0004924	abnormal behavior	Rasgef1b<em1(IMPC)J>/Rasgef1b<em1(IMPC)J>	C57BL/6NJ-Rasgef1b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461587	M	MP:0009142	decreased prepulse inhibition	Rasgef1b<em1(IMPC)J>/Rasgef1b<em1(IMPC)J>	C57BL/6NJ-Rasgef1b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461587	M	MP:0020870	decreased thigmotaxis	Rasgef1b<em1(IMPC)J>/Rasgef1b<em1(IMPC)J>	C57BL/6NJ-Rasgef1b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461588	F	MP:0001304	cataract	Rbm20<em1(IMPC)Mbp>/Rbm20<em1(IMPC)Mbp>	C57BL/6N-Rbm20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461588	F	MP:0000277	abnormal heart shape	Rbm20<em1(IMPC)Mbp>/Rbm20<em1(IMPC)Mbp>	C57BL/6N-Rbm20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461588	M	MP:0001552	increased circulating triglyceride level	Rbm20<em1(IMPC)Mbp>/Rbm20<em1(IMPC)Mbp>	C57BL/6N-Rbm20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461588	F	MP:0009084	blind uterus	Rbm20<em1(IMPC)Mbp>/Rbm20<em1(IMPC)Mbp>	C57BL/6N-Rbm20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461588	F	MP:0000692	small spleen	Rbm20<em1(IMPC)Mbp>/Rbm20<em1(IMPC)Mbp>	C57BL/6N-Rbm20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461588	F	MP:0002699	abnormal vitreous body morphology	Rbm20<em1(IMPC)Mbp>/Rbm20<em1(IMPC)Mbp>	C57BL/6N-Rbm20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461588	F	MP:0001333	absent optic nerve	Rbm20<em1(IMPC)Mbp>/Rbm20<em1(IMPC)Mbp>	C57BL/6N-Rbm20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461589	M	MP:0009142	decreased prepulse inhibition	Rbm25<em1(IMPC)J>/Rbm25<+>	C57BL/6NJ-Rbm25<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461589	M	MP:0001304	cataract	Rbm25<em1(IMPC)J>/Rbm25<+>	C57BL/6NJ-Rbm25<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461591	F	MP:0010053	decreased grip strength	Rbm6<em1(IMPC)J>/Rbm6<em1(IMPC)J>	C57BL/6NJ-Rbm6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461591	M	MP:0001488	increased startle reflex	Rbm6<em1(IMPC)J>/Rbm6<em1(IMPC)J>	C57BL/6NJ-Rbm6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461591	M	MP:0002075	abnormal coat/hair pigmentation	Rbm6<em1(IMPC)J>/Rbm6<em1(IMPC)J>	C57BL/6NJ-Rbm6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461591	F	MP:0001392	abnormal locomotor behavior	Rbm6<em1(IMPC)J>/Rbm6<em1(IMPC)J>	C57BL/6NJ-Rbm6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461593	M	MP:0002590	increased mean corpuscular volume	Relch<em1(IMPC)J>/Relch<em1(IMPC)J>	C57BL/6NJ-Relch<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461593	M	MP:0002574	increased vertical activity	Relch<em1(IMPC)J>/Relch<em1(IMPC)J>	C57BL/6NJ-Relch<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461593	F	MP:0001417	decreased exploration in new environment	Relch<em1(IMPC)J>/Relch<em1(IMPC)J>	C57BL/6NJ-Relch<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461593	M	MP:0001489	decreased startle reflex	Relch<em1(IMPC)J>/Relch<em1(IMPC)J>	C57BL/6NJ-Relch<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461593	M	MP:0001399	hyperactivity	Relch<em1(IMPC)J>/Relch<em1(IMPC)J>	C57BL/6NJ-Relch<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461594	F	MP:0001399	hyperactivity	Rell1<em1(IMPC)J>/Rell1<em1(IMPC)J>	C57BL/6NJ-Rell1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461594	M	MP:0001488	increased startle reflex	Rell1<em1(IMPC)J>/Rell1<em1(IMPC)J>	C57BL/6NJ-Rell1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461595	F	MP:0001284	absent vibrissae	Rergl<em1(IMPC)J>/Rergl<em1(IMPC)J>	C57BL/6NJ-Rergl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461595	F	MP:0001402	decreased locomotor activity	Rergl<em1(IMPC)J>/Rergl<em1(IMPC)J>	C57BL/6NJ-Rergl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461595	F	MP:0000367	abnormal coat/ hair morphology	Rergl<em1(IMPC)J>/Rergl<em1(IMPC)J>	C57BL/6NJ-Rergl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461597	M	MP:0002941	increased circulating alanine transaminase level	Retnlg<em1(IMPC)J>/Retnlg<em1(IMPC)J>	C57BL/6NJ-Retnlg<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461597	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Retnlg<em1(IMPC)J>/Retnlg<em1(IMPC)J>	C57BL/6NJ-Retnlg<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461598	M	MP:0011953	prolonged PQ interval	Rex1bd<em1(IMPC)J>/Rex1bd<em1(IMPC)J>	C57BL/6NJ-Rex1bd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461598	M	MP:0002075	abnormal coat/hair pigmentation	Rex1bd<em1(IMPC)J>/Rex1bd<em1(IMPC)J>	C57BL/6NJ-Rex1bd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461600	F	MP:0004151	decreased circulating iron level	Rhbg<em1(IMPC)Hmgu>/Rhbg<em1(IMPC)Hmgu>	C57BL/6N-Rhbg<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461601	M	MP:0001415	increased exploration in new environment	Rhoq<em1(IMPC)Mbp>/Rhoq<em1(IMPC)Mbp>	C57BL/6NCrl-Rhoq<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461601	F	MP:0001402	decreased locomotor activity	Rhoq<em1(IMPC)Mbp>/Rhoq<em1(IMPC)Mbp>	C57BL/6NCrl-Rhoq<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461605	M	MP:0000266	abnormal heart morphology	Rnase12<em1(IMPC)Mbp>/Rnase12<em1(IMPC)Mbp>	C57BL/6N-Rnase12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461605	M	MP:0000274	enlarged heart	Rnase12<em1(IMPC)Mbp>/Rnase12<em1(IMPC)Mbp>	C57BL/6N-Rnase12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461605	F	MP:0002339	abnormal lymph node morphology	Rnase12<em1(IMPC)Mbp>/Rnase12<em1(IMPC)Mbp>	C57BL/6N-Rnase12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461605	F	MP:0000702	enlarged lymph nodes	Rnase12<em1(IMPC)Mbp>/Rnase12<em1(IMPC)Mbp>	C57BL/6N-Rnase12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461605	M	MP:0000691	enlarged spleen	Rnase12<em1(IMPC)Mbp>/Rnase12<em1(IMPC)Mbp>	C57BL/6N-Rnase12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461605	M	MP:0000689	abnormal spleen morphology	Rnase12<em1(IMPC)Mbp>/Rnase12<em1(IMPC)Mbp>	C57BL/6N-Rnase12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461606	F	MP:0000470	abnormal stomach morphology	Rnase13<em1(IMPC)Mbp>/Rnase13<em1(IMPC)Mbp>	C57BL/6N-Rnase13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461606	F	MP:0011875	absent stomach	Rnase13<em1(IMPC)Mbp>/Rnase13<em1(IMPC)Mbp>	C57BL/6N-Rnase13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461606	M	MP:0002060	abnormal skin morphology	Rnase13<em1(IMPC)Mbp>/Rnase13<em1(IMPC)Mbp>	C57BL/6N-Rnase13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461606	F	MP:0000689	abnormal spleen morphology	Rnase13<em1(IMPC)Mbp>/Rnase13<em1(IMPC)Mbp>	C57BL/6N-Rnase13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461606	F	MP:0000691	enlarged spleen	Rnase13<em1(IMPC)Mbp>/Rnase13<em1(IMPC)Mbp>	C57BL/6N-Rnase13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461606	F	MP:0003883	enlarged stomach	Rnase13<em1(IMPC)Mbp>/Rnase13<em1(IMPC)Mbp>	C57BL/6N-Rnase13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461606	F	MP:0000692	small spleen	Rnase13<em1(IMPC)Mbp>/Rnase13<em1(IMPC)Mbp>	C57BL/6N-Rnase13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461607	M	MP:0002997	enlarged seminal vesicle	Rnd2<em1(IMPC)Mbp>/Rnd2<em1(IMPC)Mbp>	C57BL/6NCrl-Rnd2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461607	M	MP:0002060	abnormal skin morphology	Rnd2<em1(IMPC)Mbp>/Rnd2<em1(IMPC)Mbp>	C57BL/6NCrl-Rnd2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461607	M	MP:0000274	enlarged heart	Rnd2<em1(IMPC)Mbp>/Rnd2<em1(IMPC)Mbp>	C57BL/6NCrl-Rnd2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461607	M	MP:0011874	enlarged urinary bladder	Rnd2<em1(IMPC)Mbp>/Rnd2<em1(IMPC)Mbp>	C57BL/6NCrl-Rnd2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461607	M	MP:0001944	abnormal pancreas morphology	Rnd2<em1(IMPC)Mbp>/Rnd2<em1(IMPC)Mbp>	C57BL/6NCrl-Rnd2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461607	M	MP:0000266	abnormal heart morphology	Rnd2<em1(IMPC)Mbp>/Rnd2<em1(IMPC)Mbp>	C57BL/6NCrl-Rnd2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461607	F	MP:0010506	prolonged RR interval	Rnd2<em1(IMPC)Mbp>/Rnd2<em1(IMPC)Mbp>	C57BL/6NCrl-Rnd2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461607	M	MP:0000538	abnormal urinary bladder morphology	Rnd2<em1(IMPC)Mbp>/Rnd2<em1(IMPC)Mbp>	C57BL/6NCrl-Rnd2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461607	M	MP:0002059	abnormal seminal vesicle morphology	Rnd2<em1(IMPC)Mbp>/Rnd2<em1(IMPC)Mbp>	C57BL/6NCrl-Rnd2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461607	F	MP:0001257	increased body length	Rnd2<em1(IMPC)Mbp>/Rnd2<em1(IMPC)Mbp>	C57BL/6NCrl-Rnd2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461608	M	MP:0002574	increased vertical activity	Rnf112<tm1.1(KOMP)Vlcg>/Rnf112<tm1.1(KOMP)Vlcg>	C57BL/6N-Rnf112<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461608	M	MP:0001399	hyperactivity	Rnf112<tm1.1(KOMP)Vlcg>/Rnf112<tm1.1(KOMP)Vlcg>	C57BL/6N-Rnf112<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461609	M	MP:0000538	abnormal urinary bladder morphology	Rnf128<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Rnf128<tm1.1(KOMP)Vlcg>/Ccpcz	N	MGI:5576271
MGI:6461609	M	MP:0013772	increased effector memory T-helper cell number	Rnf128<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Rnf128<tm1.1(KOMP)Vlcg>/Ccpcz	N	MGI:5576271
MGI:6461609	M	MP:0011874	enlarged urinary bladder	Rnf128<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Rnf128<tm1.1(KOMP)Vlcg>/Ccpcz	N	MGI:5576271
MGI:6461611	F	MP:0013279	increased fasting circulating glucose level	Rnf14<em1(IMPC)Ccpcz>/Rnf14<em1(IMPC)Ccpcz>	C57BL/6N-Rnf14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461611	M	MP:0001556	increased circulating HDL cholesterol level	Rnf14<em1(IMPC)Ccpcz>/Rnf14<em1(IMPC)Ccpcz>	C57BL/6N-Rnf14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461611	F	MP:0002135	abnormal kidney morphology	Rnf14<em1(IMPC)Ccpcz>/Rnf14<em1(IMPC)Ccpcz>	C57BL/6N-Rnf14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461611	M	MP:0002060	abnormal skin morphology	Rnf14<em1(IMPC)Ccpcz>/Rnf14<em1(IMPC)Ccpcz>	C57BL/6N-Rnf14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461611	M	MP:0002834	decreased heart weight	Rnf14<em1(IMPC)Ccpcz>/Rnf14<em1(IMPC)Ccpcz>	C57BL/6N-Rnf14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461614	M	MP:0002574	increased vertical activity	Rnpepl1<em1(IMPC)Mbp>/Rnpepl1<em1(IMPC)Mbp>	C57BL/6N-Rnpepl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461614	F	MP:0001304	cataract	Rnpepl1<em1(IMPC)Mbp>/Rnpepl1<em1(IMPC)Mbp>	C57BL/6N-Rnpepl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461615	M	MP:0001364	decreased anxiety-related response	Robo1<em1(IMPC)Mbp>/Robo1<+>	C57BL/6N-Robo1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461615	M	MP:0004924	abnormal behavior	Robo1<em1(IMPC)Mbp>/Robo1<+>	C57BL/6N-Robo1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461615	M	MP:0001402	decreased locomotor activity	Robo1<em1(IMPC)Mbp>/Robo1<+>	C57BL/6N-Robo1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461615	M	MP:0020870	decreased thigmotaxis	Robo1<em1(IMPC)Mbp>/Robo1<+>	C57BL/6N-Robo1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461616	F	MP:0000703	abnormal thymus morphology	Rpap3<em1(IMPC)Mbp>/Rpap3<+>	C57BL/6N-Rpap3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461616	M	MP:0001147	small testis	Rpap3<em1(IMPC)Mbp>/Rpap3<+>	C57BL/6N-Rpap3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461616	M	MP:0005560	decreased circulating glucose level	Rpap3<em1(IMPC)Mbp>/Rpap3<+>	C57BL/6N-Rpap3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461616	F	MP:0000709	enlarged thymus	Rpap3<em1(IMPC)Mbp>/Rpap3<+>	C57BL/6N-Rpap3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461616	M	MP:0001146	abnormal testis morphology	Rpap3<em1(IMPC)Mbp>/Rpap3<+>	C57BL/6N-Rpap3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461616	M	MP:0000195	decreased circulating calcium level	Rpap3<em1(IMPC)Mbp>/Rpap3<+>	C57BL/6N-Rpap3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461616	M	MP:0000198	decreased circulating phosphate level	Rpap3<em1(IMPC)Mbp>/Rpap3<+>	C57BL/6N-Rpap3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461617	M	MP:0003984	embryonic growth retardation	Rprd2<em1(IMPC)J>/Rprd2<em1(IMPC)J>	C57BL/6NJ-Rprd2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461622	F	MP:0005293	impaired glucose tolerance	Rufy2<tm1a(EUCOMM)Wtsi>/Rufy2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Rufy2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461623	M	MP:0000691	enlarged spleen	Rufy4<em1(IMPC)Mbp>/Rufy4<em1(IMPC)Mbp>	C57BL/6N-Rufy4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461623	M	MP:0000689	abnormal spleen morphology	Rufy4<em1(IMPC)Mbp>/Rufy4<em1(IMPC)Mbp>	C57BL/6N-Rufy4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461623	F	MP:0001417	decreased exploration in new environment	Rufy4<em1(IMPC)Mbp>/Rufy4<em1(IMPC)Mbp>	C57BL/6N-Rufy4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461623	M	MP:0020421	increased freezing behavior	Rufy4<em1(IMPC)Mbp>/Rufy4<em1(IMPC)Mbp>	C57BL/6N-Rufy4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461625	F	MP:0001289	persistence of hyaloid vascular system	Rxfp3<em1(IMPC)J>/Rxfp3<em1(IMPC)J>	C57BL/6NJ-Rxfp3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461625	M	MP:0001325	abnormal retina morphology	Rxfp3<em1(IMPC)J>/Rxfp3<em1(IMPC)J>	C57BL/6NJ-Rxfp3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461626	M	MP:0000195	decreased circulating calcium level	S100a16<em1(IMPC)J>/S100a16<+>	C57BL/6NJ-S100a16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461628	M	MP:0020870	decreased thigmotaxis	Samd11<em1(IMPC)J>/Samd11<em1(IMPC)J>	C57BL/6NJ-Samd11<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461629	M	MP:0001392	abnormal locomotor behavior	Samd7<tm1b(EUCOMM)Hmgu>/Samd7<tm1b(EUCOMM)Hmgu>	C57BL/6N-Samd7<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6461633	F	MP:0001399	hyperactivity	Scg3<em1(IMPC)J>/Scg3<em1(IMPC)J>	C57BL/6NJ-Scg3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461633	F	MP:0002574	increased vertical activity	Scg3<em1(IMPC)J>/Scg3<em1(IMPC)J>	C57BL/6NJ-Scg3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461634	F	MP:0010053	decreased grip strength	Scgb1c1<em1(IMPC)J>/Scgb1c1<em1(IMPC)J>	C57BL/6NJ-Scgb1c1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461635	M	MP:0003961	decreased lean body mass	Scn11a<em1(IMPC)H>/Scn11a<em1(IMPC)H>	C57BL/6NTac-Scn11a<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461637	F	MP:0010580	decreased heart left ventricle size	Sec13<em1(IMPC)Hmgu>/Sec13<+>	C57BL/6N-Sec13<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461638	M	MP:0011962	increased cornea thickness	Sec14l5<em1(IMPC)Bay>/Sec14l5<em1(IMPC)Bay>	C57BL/6N-Sec14l5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461639	F	MP:0005343	increased circulating aspartate transaminase level	Sec31a<em3(IMPC)H>/Sec31a<+>	C57BL/6N-Sec31a<em3(IMPC)H>/H	N	MGI:5576271
MGI:6461639	F	MP:0013278	decreased fasting circulating glucose level	Sec31a<em3(IMPC)H>/Sec31a<+>	C57BL/6N-Sec31a<em3(IMPC)H>/H	N	MGI:5576271
MGI:6461639	F	MP:0002941	increased circulating alanine transaminase level	Sec31a<em3(IMPC)H>/Sec31a<+>	C57BL/6N-Sec31a<em3(IMPC)H>/H	N	MGI:5576271
MGI:6461639	F	MP:0010052	increased grip strength	Sec31a<em3(IMPC)H>/Sec31a<+>	C57BL/6N-Sec31a<em3(IMPC)H>/H	N	MGI:5576271
MGI:6461641	M	MP:0000274	enlarged heart	Sephs2<em1(IMPC)Mbp>/Sephs2<+>	C57BL/6N-Sephs2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461641	M	MP:0000266	abnormal heart morphology	Sephs2<em1(IMPC)Mbp>/Sephs2<+>	C57BL/6N-Sephs2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6461643	F	MP:0010053	decreased grip strength	Serp2<em1(IMPC)J>/Serp2<em1(IMPC)J>	C57BL/6NJ-Serp2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461644	M	MP:0002590	increased mean corpuscular volume	Serpina5<em1(IMPC)Mbp>/Serpina5<em1(IMPC)Mbp>	C57BL/6N-Serpina5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461644	M	MP:0003068	enlarged kidney	Serpina5<em1(IMPC)Mbp>/Serpina5<em1(IMPC)Mbp>	C57BL/6N-Serpina5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461644	M	MP:0002135	abnormal kidney morphology	Serpina5<em1(IMPC)Mbp>/Serpina5<em1(IMPC)Mbp>	C57BL/6N-Serpina5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461644	M	MP:0001925	male infertility	Serpina5<em1(IMPC)Mbp>/Serpina5<em1(IMPC)Mbp>	C57BL/6N-Serpina5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461645	M	MP:0000702	enlarged lymph nodes	Serpine1<em1(IMPC)Tcp>/Serpine1<em1(IMPC)Tcp>	C57BL/6N-Serpine1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461645	M	MP:0000157	abnormal sternum morphology	Serpine1<em1(IMPC)Tcp>/Serpine1<em1(IMPC)Tcp>	C57BL/6N-Serpine1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461646	F	MP:0001399	hyperactivity	Sf3b3<em1(IMPC)J>/Sf3b3<+>	C57BL/6NJ-Sf3b3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461646	F	MP:0020870	decreased thigmotaxis	Sf3b3<em1(IMPC)J>/Sf3b3<+>	C57BL/6NJ-Sf3b3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461646	F	MP:0002075	abnormal coat/hair pigmentation	Sf3b3<em1(IMPC)J>/Sf3b3<+>	C57BL/6NJ-Sf3b3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461646	F	MP:0001312	abnormal cornea morphology	Sf3b3<em1(IMPC)J>/Sf3b3<+>	C57BL/6NJ-Sf3b3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461646	F	MP:0004924	abnormal behavior	Sf3b3<em1(IMPC)J>/Sf3b3<+>	C57BL/6NJ-Sf3b3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461647	M	MP:0005333	decreased heart rate	Sfswap<em1(IMPC)J>/Sfswap<+>	C57BL/6NJ-Sfswap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461647	F	MP:0010053	decreased grip strength	Sfswap<em1(IMPC)J>/Sfswap<+>	C57BL/6NJ-Sfswap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461647	M	MP:0002941	increased circulating alanine transaminase level	Sfswap<em1(IMPC)J>/Sfswap<+>	C57BL/6NJ-Sfswap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461647	M	MP:0010506	prolonged RR interval	Sfswap<em1(IMPC)J>/Sfswap<+>	C57BL/6NJ-Sfswap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461649	F	MP:0010053	decreased grip strength	Sh3d19<em1(IMPC)J>/Sh3d19<em1(IMPC)J>	C57BL/6NJ-Sh3d19<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461650	M	MP:0010052	increased grip strength	Shc4<em1(IMPC)J>/Shc4<em1(IMPC)J>	C57BL/6NJ-Shc4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461651	F	MP:0001120	abnormal uterus morphology	Shld1<em1(IMPC)Mbp>/Shld1<em1(IMPC)Mbp>	C57BL/6NCrl-Shld1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461651	F	MP:0004906	enlarged uterus	Shld1<em1(IMPC)Mbp>/Shld1<em1(IMPC)Mbp>	C57BL/6NCrl-Shld1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461651	M	MP:0005293	impaired glucose tolerance	Shld1<em1(IMPC)Mbp>/Shld1<em1(IMPC)Mbp>	C57BL/6NCrl-Shld1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461651	F	MP:0000266	abnormal heart morphology	Shld1<em1(IMPC)Mbp>/Shld1<em1(IMPC)Mbp>	C57BL/6NCrl-Shld1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461651	M	MP:0002997	enlarged seminal vesicle	Shld1<em1(IMPC)Mbp>/Shld1<em1(IMPC)Mbp>	C57BL/6NCrl-Shld1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461651	M	MP:0001417	decreased exploration in new environment	Shld1<em1(IMPC)Mbp>/Shld1<em1(IMPC)Mbp>	C57BL/6NCrl-Shld1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461651	F	MP:0000274	enlarged heart	Shld1<em1(IMPC)Mbp>/Shld1<em1(IMPC)Mbp>	C57BL/6NCrl-Shld1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461651	F	MP:0002339	abnormal lymph node morphology	Shld1<em1(IMPC)Mbp>/Shld1<em1(IMPC)Mbp>	C57BL/6NCrl-Shld1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461651	M	MP:0003642	absent seminal vesicle	Shld1<em1(IMPC)Mbp>/Shld1<em1(IMPC)Mbp>	C57BL/6NCrl-Shld1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461651	F	MP:0000702	enlarged lymph nodes	Shld1<em1(IMPC)Mbp>/Shld1<em1(IMPC)Mbp>	C57BL/6NCrl-Shld1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461652	M	MP:0008806	increased circulating amylase level	Shmt1<tm1b(KOMP)Wtsi>/Shmt1<tm1b(KOMP)Wtsi>	C57BL/6N-Shmt1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6461652	M	MP:0002599	increased mean platelet volume	Shmt1<tm1b(KOMP)Wtsi>/Shmt1<tm1b(KOMP)Wtsi>	C57BL/6N-Shmt1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6461653	M	MP:0020870	decreased thigmotaxis	Shox2<em1(IMPC)Bay>/Shox2<+>	C57BL/6N-Shox2<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6461654	F	MP:0001399	hyperactivity	Shtn1<em1(IMPC)J>/Shtn1<em1(IMPC)J>	C57BL/6NJ-Shtn1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461654	M	MP:0003961	decreased lean body mass	Shtn1<em1(IMPC)J>/Shtn1<em1(IMPC)J>	C57BL/6NJ-Shtn1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461655	M	MP:0000274	enlarged heart	Six1<em1(IMPC)Mbp>/Six1<+>	C57BL/6N-Six1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461655	F	MP:0000692	small spleen	Six1<em1(IMPC)Mbp>/Six1<+>	C57BL/6N-Six1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461655	F	MP:0002060	abnormal skin morphology	Six1<em1(IMPC)Mbp>/Six1<+>	C57BL/6N-Six1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461655	M	MP:0009142	decreased prepulse inhibition	Six1<em1(IMPC)Mbp>/Six1<+>	C57BL/6N-Six1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461655	M	MP:0002989	small kidney	Six1<em1(IMPC)Mbp>/Six1<+>	C57BL/6N-Six1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461655	F	MP:0000221	decreased leukocyte cell number	Six1<em1(IMPC)Mbp>/Six1<+>	C57BL/6N-Six1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461655	M	MP:0000195	decreased circulating calcium level	Six1<em1(IMPC)Mbp>/Six1<+>	C57BL/6N-Six1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461655	M	MP:0000266	abnormal heart morphology	Six1<em1(IMPC)Mbp>/Six1<+>	C57BL/6N-Six1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461655	M	MP:0005333	decreased heart rate	Six1<em1(IMPC)Mbp>/Six1<+>	C57BL/6N-Six1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461655	F	MP:0003068	enlarged kidney	Six1<em1(IMPC)Mbp>/Six1<+>	C57BL/6N-Six1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461655	F	MP:0001120	abnormal uterus morphology	Six1<em1(IMPC)Mbp>/Six1<+>	C57BL/6N-Six1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461655	M	MP:0010506	prolonged RR interval	Six1<em1(IMPC)Mbp>/Six1<+>	C57BL/6N-Six1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461656	M	MP:0010579	increased heart left ventricle size	Skil<tm1b(EUCOMM)Hmgu>/Skil<tm1b(EUCOMM)Hmgu>	C57BL/6N-Skil<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6461658	F	MP:0005343	increased circulating aspartate transaminase level	Slbp<tm1.1(KOMP)Vlcg>/Slbp<+>	C57BL/6N-Slbp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461658	F	MP:0005344	increased circulating bilirubin level	Slbp<tm1.1(KOMP)Vlcg>/Slbp<+>	C57BL/6N-Slbp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461658	F	MP:0005561	increased mean corpuscular hemoglobin	Slbp<tm1.1(KOMP)Vlcg>/Slbp<+>	C57BL/6N-Slbp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461658	F	MP:0001399	hyperactivity	Slbp<tm1.1(KOMP)Vlcg>/Slbp<+>	C57BL/6N-Slbp<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461659	M	MP:0000219	increased neutrophil cell number	Slc11a1<em1(IMPC)Mbp>/Slc11a1<em1(IMPC)Mbp>	C57BL/6N-Slc11a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461659	F	MP:0000691	enlarged spleen	Slc11a1<em1(IMPC)Mbp>/Slc11a1<em1(IMPC)Mbp>	C57BL/6N-Slc11a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461659	M	MP:0005016	decreased lymphocyte cell number	Slc11a1<em1(IMPC)Mbp>/Slc11a1<em1(IMPC)Mbp>	C57BL/6N-Slc11a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461659	F	MP:0000689	abnormal spleen morphology	Slc11a1<em1(IMPC)Mbp>/Slc11a1<em1(IMPC)Mbp>	C57BL/6N-Slc11a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461660	M	MP:0000691	enlarged spleen	Slc12a5<em1(IMPC)Mbp>/Slc12a5<+>	C57BL/6N-Slc12a5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461660	M	MP:0004002	abnormal jejunum morphology	Slc12a5<em1(IMPC)Mbp>/Slc12a5<+>	C57BL/6N-Slc12a5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461660	F	MP:0010124	decreased bone mineral content	Slc12a5<em1(IMPC)Mbp>/Slc12a5<+>	C57BL/6N-Slc12a5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461660	M	MP:0000495	abnormal colon morphology	Slc12a5<em1(IMPC)Mbp>/Slc12a5<+>	C57BL/6N-Slc12a5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461660	F	MP:0000692	small spleen	Slc12a5<em1(IMPC)Mbp>/Slc12a5<+>	C57BL/6N-Slc12a5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461660	M	MP:0000470	abnormal stomach morphology	Slc12a5<em1(IMPC)Mbp>/Slc12a5<+>	C57BL/6N-Slc12a5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461660	M	MP:0003271	abnormal duodenum morphology	Slc12a5<em1(IMPC)Mbp>/Slc12a5<+>	C57BL/6N-Slc12a5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461660	F	MP:0005293	impaired glucose tolerance	Slc12a5<em1(IMPC)Mbp>/Slc12a5<+>	C57BL/6N-Slc12a5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461660	M	MP:0000689	abnormal spleen morphology	Slc12a5<em1(IMPC)Mbp>/Slc12a5<+>	C57BL/6N-Slc12a5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461660	M	MP:0002060	abnormal skin morphology	Slc12a5<em1(IMPC)Mbp>/Slc12a5<+>	C57BL/6N-Slc12a5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461661	M	MP:0005419	decreased circulating serum albumin level	Slc1a4<tm1e(KOMP)Wtsi>/Slc1a4<tm1e(KOMP)Wtsi>	C57BL/6N-Slc1a4<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461661	M	MP:0010067	increased red blood cell distribution width	Slc1a4<tm1e(KOMP)Wtsi>/Slc1a4<tm1e(KOMP)Wtsi>	C57BL/6N-Slc1a4<tm1e(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461662	M	MP:0001402	decreased locomotor activity	Slc22a3<em1(IMPC)Mbp>/Slc22a3<em1(IMPC)Mbp>	C57BL/6N-Slc22a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461662	M	MP:0001399	hyperactivity	Slc22a3<em1(IMPC)Mbp>/Slc22a3<em1(IMPC)Mbp>	C57BL/6N-Slc22a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461662	M	MP:0004924	abnormal behavior	Slc22a3<em1(IMPC)Mbp>/Slc22a3<em1(IMPC)Mbp>	C57BL/6N-Slc22a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461662	F	MP:0001293	anophthalmia	Slc22a3<em1(IMPC)Mbp>/Slc22a3<em1(IMPC)Mbp>	C57BL/6N-Slc22a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461662	F	MP:0002092	abnormal eye morphology	Slc22a3<em1(IMPC)Mbp>/Slc22a3<em1(IMPC)Mbp>	C57BL/6N-Slc22a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461662	M	MP:0001364	decreased anxiety-related response	Slc22a3<em1(IMPC)Mbp>/Slc22a3<em1(IMPC)Mbp>	C57BL/6N-Slc22a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461662	M	MP:0020870	decreased thigmotaxis	Slc22a3<em1(IMPC)Mbp>/Slc22a3<em1(IMPC)Mbp>	C57BL/6N-Slc22a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461664	F	MP:0010053	decreased grip strength	Slc27a6<em1(IMPC)J>/Slc27a6<em1(IMPC)J>	C57BL/6NJ-Slc27a6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461665	M	MP:0010579	increased heart left ventricle size	Slc2a12<em2(IMPC)Bay>/Slc2a12<em2(IMPC)Bay>	C57BL/6N-Slc2a12<em2(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461667	M	MP:0013279	increased fasting circulating glucose level	Slc30a2<em1(IMPC)Tcp>/Slc30a2<+>	C57BL/6N-Slc30a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461667	M	MP:0011874	enlarged urinary bladder	Slc30a2<em1(IMPC)Tcp>/Slc30a2<+>	C57BL/6N-Slc30a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461667	M	MP:0000157	abnormal sternum morphology	Slc30a2<em1(IMPC)Tcp>/Slc30a2<+>	C57BL/6N-Slc30a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461667	M	MP:0002060	abnormal skin morphology	Slc30a2<em1(IMPC)Tcp>/Slc30a2<+>	C57BL/6N-Slc30a2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461670	M	MP:0005655	increased aggression	Slc36a2<em1(IMPC)J>/Slc36a2<em1(IMPC)J>	C57BL/6NJ-Slc36a2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461670	F	MP:0000572	abnormal autopod morphology	Slc36a2<em1(IMPC)J>/Slc36a2<em1(IMPC)J>	C57BL/6NJ-Slc36a2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461671	F	MP:0000367	abnormal coat/ hair morphology	Slc39a10<em1(IMPC)J>/Slc39a10<+>	C57BL/6NJ-Slc39a10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461673	F	MP:0008528	polycystic kidney	Slc9a1<em1(IMPC)Mbp>/Slc9a1<+>	C57BL/6N-Slc9a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461674	M	MP:0002574	increased vertical activity	Slc9b1<em1(IMPC)Mbp>/Slc9b1<em1(IMPC)Mbp>	C57BL/6N-Slc9b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461674	M	MP:0000274	enlarged heart	Slc9b1<em1(IMPC)Mbp>/Slc9b1<em1(IMPC)Mbp>	C57BL/6N-Slc9b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461674	F	MP:0002989	small kidney	Slc9b1<em1(IMPC)Mbp>/Slc9b1<em1(IMPC)Mbp>	C57BL/6N-Slc9b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461674	F	MP:0002135	abnormal kidney morphology	Slc9b1<em1(IMPC)Mbp>/Slc9b1<em1(IMPC)Mbp>	C57BL/6N-Slc9b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461674	M	MP:0000598	abnormal liver morphology	Slc9b1<em1(IMPC)Mbp>/Slc9b1<em1(IMPC)Mbp>	C57BL/6N-Slc9b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461674	F	MP:0002188	small heart	Slc9b1<em1(IMPC)Mbp>/Slc9b1<em1(IMPC)Mbp>	C57BL/6N-Slc9b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461674	M	MP:0000599	enlarged liver	Slc9b1<em1(IMPC)Mbp>/Slc9b1<em1(IMPC)Mbp>	C57BL/6N-Slc9b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461675	F	MP:0001120	abnormal uterus morphology	Slco6d1<em1(IMPC)Tcp>/Slco6d1<em1(IMPC)Tcp>	C57BL/6N-Slco6d1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461676	F	MP:0001297	microphthalmia	Slit2<em1(IMPC)Mbp>/Slit2<+>	C57BL/6N-Slit2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461676	F	MP:0000689	abnormal spleen morphology	Slit2<em1(IMPC)Mbp>/Slit2<+>	C57BL/6N-Slit2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461676	M	MP:0003068	enlarged kidney	Slit2<em1(IMPC)Mbp>/Slit2<+>	C57BL/6N-Slit2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461676	F	MP:0000691	enlarged spleen	Slit2<em1(IMPC)Mbp>/Slit2<+>	C57BL/6N-Slit2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461676	F	MP:0009709	hydrometra	Slit2<em1(IMPC)Mbp>/Slit2<+>	C57BL/6N-Slit2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461676	M	MP:0002699	abnormal vitreous body morphology	Slit2<em1(IMPC)Mbp>/Slit2<+>	C57BL/6N-Slit2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461676	M	MP:0001304	cataract	Slit2<em1(IMPC)Mbp>/Slit2<+>	C57BL/6N-Slit2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461677	M	MP:0000702	enlarged lymph nodes	Slitrk5<em1(IMPC)Mbp>/Slitrk5<em1(IMPC)Mbp>	C57BL/6N-Slitrk5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461677	M	MP:0000538	abnormal urinary bladder morphology	Slitrk5<em1(IMPC)Mbp>/Slitrk5<em1(IMPC)Mbp>	C57BL/6N-Slitrk5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461677	M	MP:0002339	abnormal lymph node morphology	Slitrk5<em1(IMPC)Mbp>/Slitrk5<em1(IMPC)Mbp>	C57BL/6N-Slitrk5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461679	M	MP:0001284	absent vibrissae	Smarcd3<em1(IMPC)J>/Smarcd3<+>	C57BL/6NJ-Smarcd3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461679	F	MP:0010053	decreased grip strength	Smarcd3<em1(IMPC)J>/Smarcd3<+>	C57BL/6NJ-Smarcd3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461679	M	MP:0002098	abnormal vibrissa morphology	Smarcd3<em1(IMPC)J>/Smarcd3<+>	C57BL/6NJ-Smarcd3<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461681	M	MP:0002339	abnormal lymph node morphology	Smim23<em1(IMPC)Mbp>/Smim23<em1(IMPC)Mbp>	C57BL/6N-Smim23<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461681	M	MP:0000702	enlarged lymph nodes	Smim23<em1(IMPC)Mbp>/Smim23<em1(IMPC)Mbp>	C57BL/6N-Smim23<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461684	M	MP:0002092	abnormal eye morphology	Snx10<em1(IMPC)Mbp>/Snx10<em1(IMPC)Mbp>	C57BL/6NCrl-Snx10<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461685	F	MP:0009456	impaired cued conditioning behavior	Sowaha<em1(IMPC)Mbp>/Sowaha<em1(IMPC)Mbp>	C57BL/6N-Sowaha<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461685	F	MP:0002135	abnormal kidney morphology	Sowaha<em1(IMPC)Mbp>/Sowaha<em1(IMPC)Mbp>	C57BL/6N-Sowaha<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461685	F	MP:0002989	small kidney	Sowaha<em1(IMPC)Mbp>/Sowaha<em1(IMPC)Mbp>	C57BL/6N-Sowaha<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461685	M	MP:0000274	enlarged heart	Sowaha<em1(IMPC)Mbp>/Sowaha<em1(IMPC)Mbp>	C57BL/6N-Sowaha<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461685	F	MP:0000598	abnormal liver morphology	Sowaha<em1(IMPC)Mbp>/Sowaha<em1(IMPC)Mbp>	C57BL/6N-Sowaha<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461685	F	MP:0000601	small liver	Sowaha<em1(IMPC)Mbp>/Sowaha<em1(IMPC)Mbp>	C57BL/6N-Sowaha<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461685	M	MP:0000266	abnormal heart morphology	Sowaha<em1(IMPC)Mbp>/Sowaha<em1(IMPC)Mbp>	C57BL/6N-Sowaha<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461685	F	MP:0002060	abnormal skin morphology	Sowaha<em1(IMPC)Mbp>/Sowaha<em1(IMPC)Mbp>	C57BL/6N-Sowaha<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461685	M	MP:0001304	cataract	Sowaha<em1(IMPC)Mbp>/Sowaha<em1(IMPC)Mbp>	C57BL/6N-Sowaha<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461686	F	MP:0020421	increased freezing behavior	Spag11a<em1(IMPC)Mbp>/Spag11a<em1(IMPC)Mbp>	C57BL/6NCrl-Spag11a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461686	M	MP:0002574	increased vertical activity	Spag11a<em1(IMPC)Mbp>/Spag11a<em1(IMPC)Mbp>	C57BL/6NCrl-Spag11a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461686	M	MP:0000220	increased monocyte cell number	Spag11a<em1(IMPC)Mbp>/Spag11a<em1(IMPC)Mbp>	C57BL/6NCrl-Spag11a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461687	F	MP:0001120	abnormal uterus morphology	Sparcl1<em1(IMPC)Mbp>/Sparcl1<em1(IMPC)Mbp>	C57BL/6N-Sparcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461687	F	MP:0009709	hydrometra	Sparcl1<em1(IMPC)Mbp>/Sparcl1<em1(IMPC)Mbp>	C57BL/6N-Sparcl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461689	F	MP:0005553	increased circulating creatinine level	Spata3<em1(IMPC)J>/Spata3<em1(IMPC)J>	C57BL/6NJ-Spata3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461690	F	MP:0009709	hydrometra	Spata46<em1(IMPC)Mbp>/Spata46<em1(IMPC)Mbp>	C57BL/6NCrl-Spata46<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461690	M	MP:0009552	urinary bladder obstruction	Spata46<em1(IMPC)Mbp>/Spata46<em1(IMPC)Mbp>	C57BL/6NCrl-Spata46<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461690	M	MP:0000274	enlarged heart	Spata46<em1(IMPC)Mbp>/Spata46<em1(IMPC)Mbp>	C57BL/6NCrl-Spata46<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461690	F	MP:0001126	abnormal ovary morphology	Spata46<em1(IMPC)Mbp>/Spata46<em1(IMPC)Mbp>	C57BL/6NCrl-Spata46<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461690	M	MP:0000266	abnormal heart morphology	Spata46<em1(IMPC)Mbp>/Spata46<em1(IMPC)Mbp>	C57BL/6NCrl-Spata46<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461690	F	MP:0004906	enlarged uterus	Spata46<em1(IMPC)Mbp>/Spata46<em1(IMPC)Mbp>	C57BL/6NCrl-Spata46<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461690	F	MP:0004832	enlarged ovary	Spata46<em1(IMPC)Mbp>/Spata46<em1(IMPC)Mbp>	C57BL/6NCrl-Spata46<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461690	F	MP:0001120	abnormal uterus morphology	Spata46<em1(IMPC)Mbp>/Spata46<em1(IMPC)Mbp>	C57BL/6NCrl-Spata46<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461690	M	MP:0000277	abnormal heart shape	Spata46<em1(IMPC)Mbp>/Spata46<em1(IMPC)Mbp>	C57BL/6NCrl-Spata46<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461691	M	MP:0005576	decreased pulmonary ventilation	Spata6<tm1b(KOMP)Wtsi>/Spata6<tm1b(KOMP)Wtsi>	C57BL/6N-Spata6<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6461693	M	MP:0000274	enlarged heart	Sphk1<em1(IMPC)Mbp>/Sphk1<em1(IMPC)Mbp>	C57BL/6N-Sphk1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461693	F	MP:0002060	abnormal skin morphology	Sphk1<em1(IMPC)Mbp>/Sphk1<em1(IMPC)Mbp>	C57BL/6N-Sphk1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461693	F	MP:0002699	abnormal vitreous body morphology	Sphk1<em1(IMPC)Mbp>/Sphk1<em1(IMPC)Mbp>	C57BL/6N-Sphk1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461693	F	MP:0002135	abnormal kidney morphology	Sphk1<em1(IMPC)Mbp>/Sphk1<em1(IMPC)Mbp>	C57BL/6N-Sphk1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461693	M	MP:0000266	abnormal heart morphology	Sphk1<em1(IMPC)Mbp>/Sphk1<em1(IMPC)Mbp>	C57BL/6N-Sphk1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461693	F	MP:0002989	small kidney	Sphk1<em1(IMPC)Mbp>/Sphk1<em1(IMPC)Mbp>	C57BL/6N-Sphk1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461695	M	MP:0000689	abnormal spleen morphology	Spink13<em1(IMPC)Ccpcz>/Spink13<em1(IMPC)Ccpcz>	C57BL/6N-Spink13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461695	M	MP:0002135	abnormal kidney morphology	Spink13<em1(IMPC)Ccpcz>/Spink13<em1(IMPC)Ccpcz>	C57BL/6N-Spink13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461695	F	MP:0000709	enlarged thymus	Spink13<em1(IMPC)Ccpcz>/Spink13<em1(IMPC)Ccpcz>	C57BL/6N-Spink13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461695	M	MP:0003068	enlarged kidney	Spink13<em1(IMPC)Ccpcz>/Spink13<em1(IMPC)Ccpcz>	C57BL/6N-Spink13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461695	M	MP:0000266	abnormal heart morphology	Spink13<em1(IMPC)Ccpcz>/Spink13<em1(IMPC)Ccpcz>	C57BL/6N-Spink13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461695	M	MP:0003917	increased kidney weight	Spink13<em1(IMPC)Ccpcz>/Spink13<em1(IMPC)Ccpcz>	C57BL/6N-Spink13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461695	M	MP:0003604	single kidney	Spink13<em1(IMPC)Ccpcz>/Spink13<em1(IMPC)Ccpcz>	C57BL/6N-Spink13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461695	F	MP:0000703	abnormal thymus morphology	Spink13<em1(IMPC)Ccpcz>/Spink13<em1(IMPC)Ccpcz>	C57BL/6N-Spink13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461695	M	MP:0000274	enlarged heart	Spink13<em1(IMPC)Ccpcz>/Spink13<em1(IMPC)Ccpcz>	C57BL/6N-Spink13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461696	M	MP:0002135	abnormal kidney morphology	Spred2<em1(IMPC)Mbp>/Spred2<em1(IMPC)Mbp>	C57BL/6N-Spred2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461696	M	MP:0005344	increased circulating bilirubin level	Spred2<em1(IMPC)Mbp>/Spred2<em1(IMPC)Mbp>	C57BL/6N-Spred2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461696	M	MP:0003068	enlarged kidney	Spred2<em1(IMPC)Mbp>/Spred2<em1(IMPC)Mbp>	C57BL/6N-Spred2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461696	M	MP:0000274	enlarged heart	Spred2<em1(IMPC)Mbp>/Spred2<em1(IMPC)Mbp>	C57BL/6N-Spred2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461696	F	MP:0002060	abnormal skin morphology	Spred2<em1(IMPC)Mbp>/Spred2<em1(IMPC)Mbp>	C57BL/6N-Spred2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461696	F	MP:0003883	enlarged stomach	Spred2<em1(IMPC)Mbp>/Spred2<em1(IMPC)Mbp>	C57BL/6N-Spred2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461696	F	MP:0000689	abnormal spleen morphology	Spred2<em1(IMPC)Mbp>/Spred2<em1(IMPC)Mbp>	C57BL/6N-Spred2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461696	M	MP:0010067	increased red blood cell distribution width	Spred2<em1(IMPC)Mbp>/Spred2<em1(IMPC)Mbp>	C57BL/6N-Spred2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461696	M	MP:0000598	abnormal liver morphology	Spred2<em1(IMPC)Mbp>/Spred2<em1(IMPC)Mbp>	C57BL/6N-Spred2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461696	F	MP:0000702	enlarged lymph nodes	Spred2<em1(IMPC)Mbp>/Spred2<em1(IMPC)Mbp>	C57BL/6N-Spred2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461696	M	MP:0000266	abnormal heart morphology	Spred2<em1(IMPC)Mbp>/Spred2<em1(IMPC)Mbp>	C57BL/6N-Spred2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461697	F	MP:0000703	abnormal thymus morphology	Spryd4<em1(IMPC)Ccpcz>/Spryd4<em1(IMPC)Ccpcz>	C57BL/6N-Spryd4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461697	F	MP:0000274	enlarged heart	Spryd4<em1(IMPC)Ccpcz>/Spryd4<em1(IMPC)Ccpcz>	C57BL/6N-Spryd4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461697	F	MP:0000266	abnormal heart morphology	Spryd4<em1(IMPC)Ccpcz>/Spryd4<em1(IMPC)Ccpcz>	C57BL/6N-Spryd4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461697	F	MP:0000709	enlarged thymus	Spryd4<em1(IMPC)Ccpcz>/Spryd4<em1(IMPC)Ccpcz>	C57BL/6N-Spryd4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6461698	F	MP:0003984	embryonic growth retardation	Sptlc1<em1(IMPC)Bay>/Sptlc1<+>	C57BL/6N-Sptlc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461698	F	MP:0001697	abnormal embryo size	Sptlc1<em1(IMPC)Bay>/Sptlc1<+>	C57BL/6N-Sptlc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461699	M	MP:0003068	enlarged kidney	Spz1<em1(IMPC)Mbp>/Spz1<em1(IMPC)Mbp>	C57BL/6N-Spz1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461699	F	MP:0002699	abnormal vitreous body morphology	Spz1<em1(IMPC)Mbp>/Spz1<em1(IMPC)Mbp>	C57BL/6N-Spz1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461699	M	MP:0009552	urinary bladder obstruction	Spz1<em1(IMPC)Mbp>/Spz1<em1(IMPC)Mbp>	C57BL/6N-Spz1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461699	M	MP:0002833	increased heart weight	Spz1<em1(IMPC)Mbp>/Spz1<em1(IMPC)Mbp>	C57BL/6N-Spz1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461699	M	MP:0000691	enlarged spleen	Spz1<em1(IMPC)Mbp>/Spz1<em1(IMPC)Mbp>	C57BL/6N-Spz1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461699	F	MP:0000274	enlarged heart	Spz1<em1(IMPC)Mbp>/Spz1<em1(IMPC)Mbp>	C57BL/6N-Spz1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461699	F	MP:0004832	enlarged ovary	Spz1<em1(IMPC)Mbp>/Spz1<em1(IMPC)Mbp>	C57BL/6N-Spz1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461699	M	MP:0010067	increased red blood cell distribution width	Spz1<em1(IMPC)Mbp>/Spz1<em1(IMPC)Mbp>	C57BL/6N-Spz1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461699	F	MP:0001126	abnormal ovary morphology	Spz1<em1(IMPC)Mbp>/Spz1<em1(IMPC)Mbp>	C57BL/6N-Spz1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461699	M	MP:0000219	increased neutrophil cell number	Spz1<em1(IMPC)Mbp>/Spz1<em1(IMPC)Mbp>	C57BL/6N-Spz1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461699	F	MP:0002989	small kidney	Spz1<em1(IMPC)Mbp>/Spz1<em1(IMPC)Mbp>	C57BL/6N-Spz1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461699	M	MP:0000689	abnormal spleen morphology	Spz1<em1(IMPC)Mbp>/Spz1<em1(IMPC)Mbp>	C57BL/6N-Spz1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461699	M	MP:0000277	abnormal heart shape	Spz1<em1(IMPC)Mbp>/Spz1<em1(IMPC)Mbp>	C57BL/6N-Spz1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461700	F	MP:0001325	abnormal retina morphology	Srd5a2<em1(IMPC)Mbp>/Srd5a2<em1(IMPC)Mbp>	C57BL/6N-Srd5a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461700	M	MP:0000692	small spleen	Srd5a2<em1(IMPC)Mbp>/Srd5a2<em1(IMPC)Mbp>	C57BL/6N-Srd5a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461700	M	MP:0000691	enlarged spleen	Srd5a2<em1(IMPC)Mbp>/Srd5a2<em1(IMPC)Mbp>	C57BL/6N-Srd5a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461700	M	MP:0000689	abnormal spleen morphology	Srd5a2<em1(IMPC)Mbp>/Srd5a2<em1(IMPC)Mbp>	C57BL/6N-Srd5a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461700	F	MP:0002060	abnormal skin morphology	Srd5a2<em1(IMPC)Mbp>/Srd5a2<em1(IMPC)Mbp>	C57BL/6N-Srd5a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461702	F	MP:0001399	hyperactivity	Srsf5<em1(IMPC)J>/Srsf5<+>	C57BL/6NJ-Srsf5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461702	F	MP:0002075	abnormal coat/hair pigmentation	Srsf5<em1(IMPC)J>/Srsf5<+>	C57BL/6NJ-Srsf5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461702	M	MP:0001284	absent vibrissae	Srsf5<em1(IMPC)J>/Srsf5<+>	C57BL/6NJ-Srsf5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461703	F	MP:0010052	increased grip strength	Srsf6<em1(IMPC)J>/Srsf6<+>	C57BL/6NJ-Srsf6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461705	M	MP:0000367	abnormal coat/ hair morphology	St7<em1(IMPC)J>/St7<em1(IMPC)J>	C57BL/6NJ-St7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461706	M	MP:0001925	male infertility	Stap1<tm1a(KOMP)Wtsi>/Stap1<tm1a(KOMP)Wtsi>	C57BL/6N-Stap1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461707	F	MP:0002574	increased vertical activity	Stau2<em1(IMPC)Mbp>/Stau2<em1(IMPC)Mbp>	C57BL/6N-Stau2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461707	M	MP:0002608	increased hematocrit	Stau2<em1(IMPC)Mbp>/Stau2<em1(IMPC)Mbp>	C57BL/6N-Stau2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461710	F	MP:0002574	increased vertical activity	Stk35<em1(IMPC)J>/Stk35<em1(IMPC)J>	C57BL/6N-Stk35<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461710	F	MP:0001314	cornea opacity	Stk35<em1(IMPC)J>/Stk35<em1(IMPC)J>	C57BL/6N-Stk35<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461710	F	MP:0001399	hyperactivity	Stk35<em1(IMPC)J>/Stk35<em1(IMPC)J>	C57BL/6N-Stk35<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461710	M	MP:0005562	decreased mean corpuscular hemoglobin	Stk35<em1(IMPC)J>/Stk35<em1(IMPC)J>	C57BL/6N-Stk35<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461710	F	MP:0010053	decreased grip strength	Stk35<em1(IMPC)J>/Stk35<em1(IMPC)J>	C57BL/6N-Stk35<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461710	F	MP:0005542	cornea vascularization	Stk35<em1(IMPC)J>/Stk35<em1(IMPC)J>	C57BL/6N-Stk35<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461710	M	MP:0002941	increased circulating alanine transaminase level	Stk35<em1(IMPC)J>/Stk35<em1(IMPC)J>	C57BL/6N-Stk35<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461711	F	MP:0002989	small kidney	Stx11<em1(IMPC)Mbp>/Stx11<em1(IMPC)Mbp>	C57BL/6N-Stx11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461711	F	MP:0005013	increased lymphocyte cell number	Stx11<em1(IMPC)Mbp>/Stx11<em1(IMPC)Mbp>	C57BL/6N-Stx11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461711	M	MP:0000266	abnormal heart morphology	Stx11<em1(IMPC)Mbp>/Stx11<em1(IMPC)Mbp>	C57BL/6N-Stx11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461711	F	MP:0002135	abnormal kidney morphology	Stx11<em1(IMPC)Mbp>/Stx11<em1(IMPC)Mbp>	C57BL/6N-Stx11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461711	F	MP:0011110	preweaning lethality, incomplete penetrance	Stx11<em1(IMPC)Mbp>/Stx11<em1(IMPC)Mbp>	C57BL/6N-Stx11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461711	M	MP:0002833	increased heart weight	Stx11<em1(IMPC)Mbp>/Stx11<em1(IMPC)Mbp>	C57BL/6N-Stx11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461711	M	MP:0000274	enlarged heart	Stx11<em1(IMPC)Mbp>/Stx11<em1(IMPC)Mbp>	C57BL/6N-Stx11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461712	M	MP:0001406	abnormal gait	Stxbp5<em1(IMPC)Hmgu>/Stxbp5<+>	C57BL/6N-Stxbp5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461712	M	MP:0001417	decreased exploration in new environment	Stxbp5<em1(IMPC)Hmgu>/Stxbp5<+>	C57BL/6N-Stxbp5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461712	F	MP:0002135	abnormal kidney morphology	Stxbp5<em1(IMPC)Hmgu>/Stxbp5<+>	C57BL/6N-Stxbp5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461714	F	MP:0002092	abnormal eye morphology	Suclg2<em1(IMPC)Mbp>/Suclg2<em1(IMPC)Mbp>	C57BL/6NCrl-Suclg2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461716	F	MP:0010067	increased red blood cell distribution width	Susd1<em1(IMPC)H>/Susd1<em1(IMPC)H>	C57BL/6NTac-Susd1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461716	F	MP:0005562	decreased mean corpuscular hemoglobin	Susd1<em1(IMPC)H>/Susd1<em1(IMPC)H>	C57BL/6NTac-Susd1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461716	F	MP:0011239	abnormal skin coloration	Susd1<em1(IMPC)H>/Susd1<em1(IMPC)H>	C57BL/6NTac-Susd1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461717	M	MP:0005575	increased pulmonary ventilation	Semg1<tm1.1(KOMP)Vlcg>/Semg1<tm1.1(KOMP)Vlcg>	C57BL/6N-Semg1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461718	F	MP:0001120	abnormal uterus morphology	Sybu<em1(IMPC)Mbp>/Sybu<em1(IMPC)Mbp>	C57BL/6N-Sybu<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461718	F	MP:0009709	hydrometra	Sybu<em1(IMPC)Mbp>/Sybu<em1(IMPC)Mbp>	C57BL/6N-Sybu<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461720	M	MP:0005016	decreased lymphocyte cell number	Synpo2<tm1b(EUCOMM)Wtsi>/Synpo2<+>	C57BL/6N-Synpo2<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6461720	M	MP:0002875	decreased erythrocyte cell number	Synpo2<tm1b(EUCOMM)Wtsi>/Synpo2<+>	C57BL/6N-Synpo2<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6461720	M	MP:0000208	decreased hematocrit	Synpo2<tm1b(EUCOMM)Wtsi>/Synpo2<+>	C57BL/6N-Synpo2<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6461720	M	MP:0002874	decreased hemoglobin content	Synpo2<tm1b(EUCOMM)Wtsi>/Synpo2<+>	C57BL/6N-Synpo2<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6461720	M	MP:0000219	increased neutrophil cell number	Synpo2<tm1b(EUCOMM)Wtsi>/Synpo2<+>	C57BL/6N-Synpo2<tm1b(EUCOMM)Wtsi>/Ics	N	MGI:5576271
MGI:6461722	F	MP:0005573	increased pulmonary respiratory rate	Syt17<tm1b(KOMP)Wtsi>/Syt17<tm1b(KOMP)Wtsi>	C57BL/6N-Syt17<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6461723	M	MP:0001417	decreased exploration in new environment	Syt9<em1(IMPC)Tcp>/Syt9<em1(IMPC)Tcp>	C57BL/6N-Syt9<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461723	M	MP:0010067	increased red blood cell distribution width	Syt9<em1(IMPC)Tcp>/Syt9<em1(IMPC)Tcp>	C57BL/6N-Syt9<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461723	M	MP:0001891	hydrocephaly	Syt9<em1(IMPC)Tcp>/Syt9<em1(IMPC)Tcp>	C57BL/6N-Syt9<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461724	M	MP:0005576	decreased pulmonary ventilation	Taar6<tm1.1(KOMP)Vlcg>/Taar6<tm1.1(KOMP)Vlcg>	C57BL/6N-Taar6<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461724	M	MP:0012125	decreased bronchoconstrictive response	Taar6<tm1.1(KOMP)Vlcg>/Taar6<tm1.1(KOMP)Vlcg>	C57BL/6N-Taar6<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461724	M	MP:0005573	increased pulmonary respiratory rate	Taar6<tm1.1(KOMP)Vlcg>/Taar6<tm1.1(KOMP)Vlcg>	C57BL/6N-Taar6<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461725	M	MP:0002968	increased circulating alkaline phosphatase level	Tafa4<em1(IMPC)Mbp>/Tafa4<em1(IMPC)Mbp>	C57BL/6N-Tafa4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461725	F	MP:0002608	increased hematocrit	Tafa4<em1(IMPC)Mbp>/Tafa4<em1(IMPC)Mbp>	C57BL/6N-Tafa4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461726	M	MP:0004924	abnormal behavior	Tanc2<em1(IMPC)Hmgu>/Tanc2<em1(IMPC)Hmgu>	C57BL/6NCrl-Tanc2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461726	M	MP:0020870	decreased thigmotaxis	Tanc2<em1(IMPC)Hmgu>/Tanc2<em1(IMPC)Hmgu>	C57BL/6NCrl-Tanc2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461726	F	MP:0002764	short tibia	Tanc2<em1(IMPC)Hmgu>/Tanc2<em1(IMPC)Hmgu>	C57BL/6NCrl-Tanc2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461726	M	MP:0001399	hyperactivity	Tanc2<em1(IMPC)Hmgu>/Tanc2<em1(IMPC)Hmgu>	C57BL/6NCrl-Tanc2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461726	F	MP:0001415	increased exploration in new environment	Tanc2<em1(IMPC)Hmgu>/Tanc2<em1(IMPC)Hmgu>	C57BL/6NCrl-Tanc2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461726	M	MP:0005293	impaired glucose tolerance	Tanc2<em1(IMPC)Hmgu>/Tanc2<em1(IMPC)Hmgu>	C57BL/6NCrl-Tanc2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461726	M	MP:0002968	increased circulating alkaline phosphatase level	Tanc2<em1(IMPC)Hmgu>/Tanc2<em1(IMPC)Hmgu>	C57BL/6NCrl-Tanc2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461726	M	MP:0001392	abnormal locomotor behavior	Tanc2<em1(IMPC)Hmgu>/Tanc2<em1(IMPC)Hmgu>	C57BL/6NCrl-Tanc2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461729	F	MP:0001399	hyperactivity	Tas2r103<em1(IMPC)J>/Tas2r103<em1(IMPC)J>	C57BL/6NJ-Tas2r103<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461730	M	MP:0001529	abnormal vocalization	Tasor2<em1(IMPC)J>/Tasor2<em1(IMPC)J>	C57BL/6NJ-Tasor2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461730	M	MP:0002075	abnormal coat/hair pigmentation	Tasor2<em1(IMPC)J>/Tasor2<em1(IMPC)J>	C57BL/6NJ-Tasor2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461731	F	MP:0010053	decreased grip strength	Tbcel<em1(IMPC)J>/Tbcel<em1(IMPC)J>	C57BL/6NJ-Tbcel<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461731	F	MP:0008259	abnormal optic disk morphology	Tbcel<em1(IMPC)J>/Tbcel<em1(IMPC)J>	C57BL/6NJ-Tbcel<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461732	M	MP:0002188	small heart	Tbx20<em1(IMPC)Mbp>/Tbx20<+>	C57BL/6N-Tbx20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461732	M	MP:0000219	increased neutrophil cell number	Tbx20<em1(IMPC)Mbp>/Tbx20<+>	C57BL/6N-Tbx20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461732	M	MP:0000266	abnormal heart morphology	Tbx20<em1(IMPC)Mbp>/Tbx20<+>	C57BL/6N-Tbx20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461733	F	MP:0002092	abnormal eye morphology	Tctn1<em1(IMPC)Mbp>/Tctn1<+>	C57BL/6NCrl-Tctn1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461734	M	MP:0013278	decreased fasting circulating glucose level	Tdrkh<tm1b(KOMP)Wtsi>/Tdrkh<tm1b(KOMP)Wtsi>	C57BL/6N-Tdrkh<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461734	M	MP:0001488	increased startle reflex	Tdrkh<tm1b(KOMP)Wtsi>/Tdrkh<tm1b(KOMP)Wtsi>	C57BL/6N-Tdrkh<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6461736	M	MP:0002941	increased circulating alanine transaminase level	Tesk1<em1(IMPC)J>/Tesk1<em1(IMPC)J>	C57BL/6NJ-Tesk1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461737	M	MP:0000221	decreased leukocyte cell number	Tex2<tm1.1(KOMP)Vlcg>/Tex2<+>	C57BL/6N-Tex2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461737	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Tex2<tm1.1(KOMP)Vlcg>/Tex2<+>	C57BL/6N-Tex2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461737	M	MP:0002590	increased mean corpuscular volume	Tex2<tm1.1(KOMP)Vlcg>/Tex2<+>	C57BL/6N-Tex2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461737	F	MP:0005560	decreased circulating glucose level	Tex2<tm1.1(KOMP)Vlcg>/Tex2<+>	C57BL/6N-Tex2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461737	M	MP:0000195	decreased circulating calcium level	Tex2<tm1.1(KOMP)Vlcg>/Tex2<+>	C57BL/6N-Tex2<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6461740	M	MP:0012125	decreased bronchoconstrictive response	Thpo<tm1.1(KOMP)Vlcg>/Thpo<tm1.1(KOMP)Vlcg>	C57BL/6N-Thpo<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461741	F	MP:0005655	increased aggression	Thsd4<em1(IMPC)J>/Thsd4<em1(IMPC)J>	C57BL/6NJ-Thsd4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461741	F	MP:0001392	abnormal locomotor behavior	Thsd4<em1(IMPC)J>/Thsd4<em1(IMPC)J>	C57BL/6NJ-Thsd4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461742	F	MP:0001259	abnormal body weight	Timp2<em1(IMPC)Hmgu>/Timp2<em1(IMPC)Hmgu>	C57BL/6N-Timp2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461742	M	MP:0000556	abnormal hindlimb morphology	Timp2<em1(IMPC)Hmgu>/Timp2<em1(IMPC)Hmgu>	C57BL/6N-Timp2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461742	M	MP:0008173	increased follicular B cell number	Timp2<em1(IMPC)Hmgu>/Timp2<em1(IMPC)Hmgu>	C57BL/6N-Timp2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461742	M	MP:0011940	decreased food intake	Timp2<em1(IMPC)Hmgu>/Timp2<em1(IMPC)Hmgu>	C57BL/6N-Timp2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461742	M	MP:0010053	decreased grip strength	Timp2<em1(IMPC)Hmgu>/Timp2<em1(IMPC)Hmgu>	C57BL/6N-Timp2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461742	F	MP:0003604	single kidney	Timp2<em1(IMPC)Hmgu>/Timp2<em1(IMPC)Hmgu>	C57BL/6N-Timp2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461742	M	MP:0011965	decreased total retina thickness	Timp2<em1(IMPC)Hmgu>/Timp2<em1(IMPC)Hmgu>	C57BL/6N-Timp2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461742	M	MP:0001486	abnormal startle reflex	Timp2<em1(IMPC)Hmgu>/Timp2<em1(IMPC)Hmgu>	C57BL/6N-Timp2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461742	F	MP:0012320	abnormal body fat mass	Timp2<em1(IMPC)Hmgu>/Timp2<em1(IMPC)Hmgu>	C57BL/6N-Timp2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461743	F	MP:0003731	abnormal retina outer nuclear layer morphology	Tlcd3b<em1(IMPC)Bay>/Tlcd3b<em1(IMPC)Bay>	C57BL/6N-Tlcd3b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461743	M	MP:0001258	decreased body length	Tlcd3b<em1(IMPC)Bay>/Tlcd3b<em1(IMPC)Bay>	C57BL/6N-Tlcd3b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461746	F	MP:0000218	increased leukocyte cell number	Tmco1<em1(IMPC)J>/Tmco1<+>	C57BL/6NJ-Tmco1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461746	M	MP:0001314	cornea opacity	Tmco1<em1(IMPC)J>/Tmco1<+>	C57BL/6NJ-Tmco1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461747	F	MP:0002968	increased circulating alkaline phosphatase level	Tmem131<em1(IMPC)J>/Tmem131<+>	C57BL/6NJ-Tmem131<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461747	F	MP:0002075	abnormal coat/hair pigmentation	Tmem131<em1(IMPC)J>/Tmem131<+>	C57BL/6NJ-Tmem131<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461747	F	MP:0010053	decreased grip strength	Tmem131<em1(IMPC)J>/Tmem131<+>	C57BL/6NJ-Tmem131<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461748	M	MP:0002941	increased circulating alanine transaminase level	Tmem145<em1(IMPC)Mbp>/Tmem145<em1(IMPC)Mbp>	C57BL/6N-Tmem145<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461748	M	MP:0001304	cataract	Tmem145<em1(IMPC)Mbp>/Tmem145<em1(IMPC)Mbp>	C57BL/6N-Tmem145<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461748	M	MP:0002188	small heart	Tmem145<em1(IMPC)Mbp>/Tmem145<em1(IMPC)Mbp>	C57BL/6N-Tmem145<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461748	F	MP:0002135	abnormal kidney morphology	Tmem145<em1(IMPC)Mbp>/Tmem145<em1(IMPC)Mbp>	C57BL/6N-Tmem145<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461748	M	MP:0002699	abnormal vitreous body morphology	Tmem145<em1(IMPC)Mbp>/Tmem145<em1(IMPC)Mbp>	C57BL/6N-Tmem145<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461748	M	MP:0000266	abnormal heart morphology	Tmem145<em1(IMPC)Mbp>/Tmem145<em1(IMPC)Mbp>	C57BL/6N-Tmem145<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461748	F	MP:0001325	abnormal retina morphology	Tmem145<em1(IMPC)Mbp>/Tmem145<em1(IMPC)Mbp>	C57BL/6N-Tmem145<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461748	F	MP:0002989	small kidney	Tmem145<em1(IMPC)Mbp>/Tmem145<em1(IMPC)Mbp>	C57BL/6N-Tmem145<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461749	M	MP:0002075	abnormal coat/hair pigmentation	Tmem175<tm1b(KOMP)Wtsi>/Tmem175<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem175<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6461749	F	MP:0005343	increased circulating aspartate transaminase level	Tmem175<tm1b(KOMP)Wtsi>/Tmem175<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem175<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6461749	M	MP:0002059	abnormal seminal vesicle morphology	Tmem175<tm1b(KOMP)Wtsi>/Tmem175<tm1b(KOMP)Wtsi>	C57BL/6N-Tmem175<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6461750	F	MP:0020420	abnormal freezing behavior	Tmem225<em1(IMPC)Mbp>/Tmem225<em1(IMPC)Mbp>	C57BL/6N-Tmem225<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461750	M	MP:0000274	enlarged heart	Tmem225<em1(IMPC)Mbp>/Tmem225<em1(IMPC)Mbp>	C57BL/6N-Tmem225<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461750	M	MP:0001925	male infertility	Tmem225<em1(IMPC)Mbp>/Tmem225<em1(IMPC)Mbp>	C57BL/6N-Tmem225<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461750	M	MP:0002699	abnormal vitreous body morphology	Tmem225<em1(IMPC)Mbp>/Tmem225<em1(IMPC)Mbp>	C57BL/6N-Tmem225<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461750	M	MP:0000692	small spleen	Tmem225<em1(IMPC)Mbp>/Tmem225<em1(IMPC)Mbp>	C57BL/6N-Tmem225<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461750	F	MP:0002188	small heart	Tmem225<em1(IMPC)Mbp>/Tmem225<em1(IMPC)Mbp>	C57BL/6N-Tmem225<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461750	M	MP:0001304	cataract	Tmem225<em1(IMPC)Mbp>/Tmem225<em1(IMPC)Mbp>	C57BL/6N-Tmem225<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461752	F	MP:0000692	small spleen	Tmem45a<em1(IMPC)Mbp>/Tmem45a<em1(IMPC)Mbp>	C57BL/6N-Tmem45a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461752	M	MP:0010053	decreased grip strength	Tmem45a<em1(IMPC)Mbp>/Tmem45a<em1(IMPC)Mbp>	C57BL/6N-Tmem45a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461752	M	MP:0001146	abnormal testis morphology	Tmem45a<em1(IMPC)Mbp>/Tmem45a<em1(IMPC)Mbp>	C57BL/6N-Tmem45a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461752	M	MP:0000691	enlarged spleen	Tmem45a<em1(IMPC)Mbp>/Tmem45a<em1(IMPC)Mbp>	C57BL/6N-Tmem45a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461752	M	MP:0001147	small testis	Tmem45a<em1(IMPC)Mbp>/Tmem45a<em1(IMPC)Mbp>	C57BL/6N-Tmem45a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461753	M	MP:0011874	enlarged urinary bladder	Tmem8b<em1(IMPC)Tcp>/Tmem8b<+>	C57BL/6N-Tmem8b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461753	M	MP:0000157	abnormal sternum morphology	Tmem8b<em1(IMPC)Tcp>/Tmem8b<+>	C57BL/6N-Tmem8b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461753	F	MP:0001126	abnormal ovary morphology	Tmem8b<em1(IMPC)Tcp>/Tmem8b<+>	C57BL/6N-Tmem8b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461753	M	MP:0002606	increased basophil cell number	Tmem8b<em1(IMPC)Tcp>/Tmem8b<+>	C57BL/6N-Tmem8b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461753	F	MP:0009142	decreased prepulse inhibition	Tmem8b<em1(IMPC)Tcp>/Tmem8b<+>	C57BL/6N-Tmem8b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461753	M	MP:0001258	decreased body length	Tmem8b<em1(IMPC)Tcp>/Tmem8b<+>	C57BL/6N-Tmem8b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461755	M	MP:0001486	abnormal startle reflex	Tmie<em1(IMPC)J>/Tmie<em1(IMPC)J>	C57BL/6NJ-Tmie<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461755	M	MP:0004924	abnormal behavior	Tmie<em1(IMPC)J>/Tmie<em1(IMPC)J>	C57BL/6NJ-Tmie<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461755	M	MP:0001410	head bobbing	Tmie<em1(IMPC)J>/Tmie<em1(IMPC)J>	C57BL/6NJ-Tmie<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461755	M	MP:0005655	increased aggression	Tmie<em1(IMPC)J>/Tmie<em1(IMPC)J>	C57BL/6NJ-Tmie<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461757	F	MP:0002989	small kidney	Tnfaip8l1<em1(IMPC)Mbp>/Tnfaip8l1<em1(IMPC)Mbp>	C57BL/6N-Tnfaip8l1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461757	M	MP:0000692	small spleen	Tnfaip8l1<em1(IMPC)Mbp>/Tnfaip8l1<em1(IMPC)Mbp>	C57BL/6N-Tnfaip8l1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461757	M	MP:0000538	abnormal urinary bladder morphology	Tnfaip8l1<em1(IMPC)Mbp>/Tnfaip8l1<em1(IMPC)Mbp>	C57BL/6N-Tnfaip8l1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461757	F	MP:0002060	abnormal skin morphology	Tnfaip8l1<em1(IMPC)Mbp>/Tnfaip8l1<em1(IMPC)Mbp>	C57BL/6N-Tnfaip8l1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461757	F	MP:0000601	small liver	Tnfaip8l1<em1(IMPC)Mbp>/Tnfaip8l1<em1(IMPC)Mbp>	C57BL/6N-Tnfaip8l1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461757	M	MP:0000599	enlarged liver	Tnfaip8l1<em1(IMPC)Mbp>/Tnfaip8l1<em1(IMPC)Mbp>	C57BL/6N-Tnfaip8l1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461757	F	MP:0002135	abnormal kidney morphology	Tnfaip8l1<em1(IMPC)Mbp>/Tnfaip8l1<em1(IMPC)Mbp>	C57BL/6N-Tnfaip8l1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461757	M	MP:0001486	abnormal startle reflex	Tnfaip8l1<em1(IMPC)Mbp>/Tnfaip8l1<em1(IMPC)Mbp>	C57BL/6N-Tnfaip8l1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461757	F	MP:0002092	abnormal eye morphology	Tnfaip8l1<em1(IMPC)Mbp>/Tnfaip8l1<em1(IMPC)Mbp>	C57BL/6N-Tnfaip8l1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	F	MP:0010053	decreased grip strength	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	F	MP:0003795	abnormal bone structure	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	F	MP:0001314	cornea opacity	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	F	MP:0001293	anophthalmia	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	F	MP:0002152	abnormal brain morphology	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	M	MP:0003068	enlarged kidney	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	F	MP:0000774	decreased brain size	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	M	MP:0001406	abnormal gait	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	F	MP:0002060	abnormal skin morphology	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	M	MP:0000692	small spleen	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	F	MP:0002092	abnormal eye morphology	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	M	MP:0002135	abnormal kidney morphology	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	F	MP:0009084	blind uterus	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	F	MP:0002699	abnormal vitreous body morphology	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	F	MP:0011110	preweaning lethality, incomplete penetrance	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461758	F	MP:0001258	decreased body length	Tnfrsf11b<em1(IMPC)Mbp>/Tnfrsf11b<em1(IMPC)Mbp>	C57BL/6N-Tnfrsf11b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461759	M	MP:0010025	decreased total body fat amount	Tnk1<tm1b(EUCOMM)Hmgu>/Tnk1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Tnk1<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461760	F	MP:0000702	enlarged lymph nodes	Tnk2<em1(IMPC)Tcp>/Tnk2<em1(IMPC)Tcp>	C57BL/6N-Tnk2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461761	M	MP:0002757	decreased vertical activity	Tnks<em1(IMPC)Hmgu>/Tnks<em1(IMPC)Hmgu>	C57BL/6N-Tnks<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461761	M	MP:0001891	hydrocephaly	Tnks<em1(IMPC)Hmgu>/Tnks<em1(IMPC)Hmgu>	C57BL/6N-Tnks<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461761	F	MP:0005560	decreased circulating glucose level	Tnks<em1(IMPC)Hmgu>/Tnks<em1(IMPC)Hmgu>	C57BL/6N-Tnks<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461761	F	MP:0010124	decreased bone mineral content	Tnks<em1(IMPC)Hmgu>/Tnks<em1(IMPC)Hmgu>	C57BL/6N-Tnks<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461761	M	MP:0002968	increased circulating alkaline phosphatase level	Tnks<em1(IMPC)Hmgu>/Tnks<em1(IMPC)Hmgu>	C57BL/6N-Tnks<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461761	F	MP:0002590	increased mean corpuscular volume	Tnks<em1(IMPC)Hmgu>/Tnks<em1(IMPC)Hmgu>	C57BL/6N-Tnks<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461761	F	MP:0000186	decreased circulating HDL cholesterol level	Tnks<em1(IMPC)Hmgu>/Tnks<em1(IMPC)Hmgu>	C57BL/6N-Tnks<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461761	F	MP:0010053	decreased grip strength	Tnks<em1(IMPC)Hmgu>/Tnks<em1(IMPC)Hmgu>	C57BL/6N-Tnks<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461761	M	MP:0001325	abnormal retina morphology	Tnks<em1(IMPC)Hmgu>/Tnks<em1(IMPC)Hmgu>	C57BL/6N-Tnks<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461761	F	MP:0010025	decreased total body fat amount	Tnks<em1(IMPC)Hmgu>/Tnks<em1(IMPC)Hmgu>	C57BL/6N-Tnks<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461761	M	MP:0011965	decreased total retina thickness	Tnks<em1(IMPC)Hmgu>/Tnks<em1(IMPC)Hmgu>	C57BL/6N-Tnks<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461761	F	MP:0005179	decreased circulating cholesterol level	Tnks<em1(IMPC)Hmgu>/Tnks<em1(IMPC)Hmgu>	C57BL/6N-Tnks<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461761	M	MP:0005343	increased circulating aspartate transaminase level	Tnks<em1(IMPC)Hmgu>/Tnks<em1(IMPC)Hmgu>	C57BL/6N-Tnks<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461764	M	MP:0006243	impaired pupillary reflex	Top3a<tm1b(EUCOMM)Hmgu>/Top3a<+>	C57BL/6N-Top3a<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6461766	M	MP:0002875	decreased erythrocyte cell number	Trank1<em1(IMPC)J>/Trank1<em1(IMPC)J>	C57BL/6NJ-Trank1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461766	M	MP:0005554	decreased circulating creatinine level	Trank1<em1(IMPC)J>/Trank1<em1(IMPC)J>	C57BL/6NJ-Trank1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461766	M	MP:0002874	decreased hemoglobin content	Trank1<em1(IMPC)J>/Trank1<em1(IMPC)J>	C57BL/6NJ-Trank1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461766	M	MP:0000208	decreased hematocrit	Trank1<em1(IMPC)J>/Trank1<em1(IMPC)J>	C57BL/6NJ-Trank1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461770	F	MP:0002339	abnormal lymph node morphology	Trim58<em1(IMPC)Mbp>/Trim58<em1(IMPC)Mbp>	C57BL/6N-Trim58<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461770	M	MP:0003068	enlarged kidney	Trim58<em1(IMPC)Mbp>/Trim58<em1(IMPC)Mbp>	C57BL/6N-Trim58<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461770	F	MP:0000702	enlarged lymph nodes	Trim58<em1(IMPC)Mbp>/Trim58<em1(IMPC)Mbp>	C57BL/6N-Trim58<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461770	M	MP:0002135	abnormal kidney morphology	Trim58<em1(IMPC)Mbp>/Trim58<em1(IMPC)Mbp>	C57BL/6N-Trim58<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461770	F	MP:0002060	abnormal skin morphology	Trim58<em1(IMPC)Mbp>/Trim58<em1(IMPC)Mbp>	C57BL/6N-Trim58<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461770	M	MP:0002590	increased mean corpuscular volume	Trim58<em1(IMPC)Mbp>/Trim58<em1(IMPC)Mbp>	C57BL/6N-Trim58<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461772	M	MP:0010024	increased total body fat amount	Trpa1<em1(IMPC)J>/Trpa1<em1(IMPC)J>	C57BL/6NJ-Trpa1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461772	M	MP:0001529	abnormal vocalization	Trpa1<em1(IMPC)J>/Trpa1<em1(IMPC)J>	C57BL/6NJ-Trpa1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461772	M	MP:0003961	decreased lean body mass	Trpa1<em1(IMPC)J>/Trpa1<em1(IMPC)J>	C57BL/6NJ-Trpa1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461773	F	MP:0004952	increased spleen weight	Trpc1<em1(IMPC)H>/Trpc1<em1(IMPC)H>	C57BL/6N-Trpc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461773	M	MP:0002968	increased circulating alkaline phosphatase level	Trpc1<em1(IMPC)H>/Trpc1<em1(IMPC)H>	C57BL/6N-Trpc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461774	F	MP:0001399	hyperactivity	Trpm3<em1(IMPC)J>/Trpm3<em1(IMPC)J>	C57BL/6NJ-Trpm3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461775	M	MP:0013278	decreased fasting circulating glucose level	Trps1<em1(IMPC)Wtsi>/Trps1<+>	C57BL/6N-Trps1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461776	M	MP:0001529	abnormal vocalization	Tspyl1<em1(IMPC)J>/Tspyl1<+>	C57BL/6NJ-Tspyl1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461776	M	MP:0001392	abnormal locomotor behavior	Tspyl1<em1(IMPC)J>/Tspyl1<+>	C57BL/6NJ-Tspyl1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461776	M	MP:0005655	increased aggression	Tspyl1<em1(IMPC)J>/Tspyl1<+>	C57BL/6NJ-Tspyl1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461777	M	MP:0001513	limb grasping	Tspyl4<em1(IMPC)J>/Tspyl4<em1(IMPC)J>	C57BL/6NJ-Tspyl4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461777	F	MP:0001392	abnormal locomotor behavior	Tspyl4<em1(IMPC)J>/Tspyl4<em1(IMPC)J>	C57BL/6NJ-Tspyl4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461777	F	MP:0005655	increased aggression	Tspyl4<em1(IMPC)J>/Tspyl4<em1(IMPC)J>	C57BL/6NJ-Tspyl4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461779	M	MP:0005293	impaired glucose tolerance	Ttll10<tm1b(EUCOMM)Hmgu>/Ttll10<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ttll10<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6461780	M	MP:0001417	decreased exploration in new environment	Ttl<tm1b(EUCOMM)Wtsi>/Ttl<+>	C57BL/6N-Ttl<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6461781	F	MP:0001284	absent vibrissae	Tubgcp4<em1(IMPC)J>/Tubgcp4<+>	C57BL/6NJ-Tubgcp4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461781	M	MP:0001399	hyperactivity	Tubgcp4<em1(IMPC)J>/Tubgcp4<+>	C57BL/6NJ-Tubgcp4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461781	F	MP:0002098	abnormal vibrissa morphology	Tubgcp4<em1(IMPC)J>/Tubgcp4<+>	C57BL/6NJ-Tubgcp4<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461783	F	MP:0001120	abnormal uterus morphology	Tulp4<em1(IMPC)Mbp>/Tulp4<+>	C57BL/6NCrl-Tulp4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461783	F	MP:0009709	hydrometra	Tulp4<em1(IMPC)Mbp>/Tulp4<+>	C57BL/6NCrl-Tulp4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461783	F	MP:0009455	enhanced cued conditioning behavior	Tulp4<em1(IMPC)Mbp>/Tulp4<+>	C57BL/6NCrl-Tulp4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461783	M	MP:0000538	abnormal urinary bladder morphology	Tulp4<em1(IMPC)Mbp>/Tulp4<+>	C57BL/6NCrl-Tulp4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461785	F	MP:0003131	increased erythrocyte cell number	Ubac1<em1(IMPC)J>/Ubac1<em1(IMPC)J>	C57BL/6NJ-Ubac1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461785	F	MP:0005542	cornea vascularization	Ubac1<em1(IMPC)J>/Ubac1<em1(IMPC)J>	C57BL/6NJ-Ubac1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461785	F	MP:0005287	narrow eye opening	Ubac1<em1(IMPC)J>/Ubac1<em1(IMPC)J>	C57BL/6NJ-Ubac1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461787	M	MP:0002833	increased heart weight	Ube2f<em1(IMPC)Mbp>/Ube2f<+>	C57BL/6NCrl-Ube2f<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461787	M	MP:0000598	abnormal liver morphology	Ube2f<em1(IMPC)Mbp>/Ube2f<+>	C57BL/6NCrl-Ube2f<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461787	M	MP:0000274	enlarged heart	Ube2f<em1(IMPC)Mbp>/Ube2f<+>	C57BL/6NCrl-Ube2f<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461787	F	MP:0000277	abnormal heart shape	Ube2f<em1(IMPC)Mbp>/Ube2f<+>	C57BL/6NCrl-Ube2f<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461788	F	MP:0000157	abnormal sternum morphology	Ubl7<em1(IMPC)Tcp>/Ubl7<em1(IMPC)Tcp>	C57BL/6N-Ubl7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461788	F	MP:0001399	hyperactivity	Ubl7<em1(IMPC)Tcp>/Ubl7<em1(IMPC)Tcp>	C57BL/6N-Ubl7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461788	F	MP:0002608	increased hematocrit	Ubl7<em1(IMPC)Tcp>/Ubl7<em1(IMPC)Tcp>	C57BL/6N-Ubl7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461788	F	MP:0005287	narrow eye opening	Ubl7<em1(IMPC)Tcp>/Ubl7<em1(IMPC)Tcp>	C57BL/6N-Ubl7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461788	F	MP:0005564	increased hemoglobin content	Ubl7<em1(IMPC)Tcp>/Ubl7<em1(IMPC)Tcp>	C57BL/6N-Ubl7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461788	F	MP:0001297	microphthalmia	Ubl7<em1(IMPC)Tcp>/Ubl7<em1(IMPC)Tcp>	C57BL/6N-Ubl7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461788	F	MP:0005565	increased blood urea nitrogen level	Ubl7<em1(IMPC)Tcp>/Ubl7<em1(IMPC)Tcp>	C57BL/6N-Ubl7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461788	F	MP:0001944	abnormal pancreas morphology	Ubl7<em1(IMPC)Tcp>/Ubl7<em1(IMPC)Tcp>	C57BL/6N-Ubl7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461788	M	MP:0001925	male infertility	Ubl7<em1(IMPC)Tcp>/Ubl7<em1(IMPC)Tcp>	C57BL/6N-Ubl7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461788	F	MP:0005561	increased mean corpuscular hemoglobin	Ubl7<em1(IMPC)Tcp>/Ubl7<em1(IMPC)Tcp>	C57BL/6N-Ubl7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461789	F	MP:0010052	increased grip strength	Ubxn7<tm1b(EUCOMM)Wtsi>/Ubxn7<+>	C57BL/6N-Ubxn7<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6461790	F	MP:0001120	abnormal uterus morphology	Ufsp2<em1(IMPC)Mbp>/Ufsp2<+>	C57BL/6NCrl-Ufsp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461790	F	MP:0009709	hydrometra	Ufsp2<em1(IMPC)Mbp>/Ufsp2<+>	C57BL/6NCrl-Ufsp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461791	F	MP:0000266	abnormal heart morphology	Uggt1<em1(IMPC)Mbp>/Uggt1<+>	C57BL/6N-Uggt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461791	F	MP:0002989	small kidney	Uggt1<em1(IMPC)Mbp>/Uggt1<+>	C57BL/6N-Uggt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461791	F	MP:0002188	small heart	Uggt1<em1(IMPC)Mbp>/Uggt1<+>	C57BL/6N-Uggt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461791	M	MP:0000598	abnormal liver morphology	Uggt1<em1(IMPC)Mbp>/Uggt1<+>	C57BL/6N-Uggt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461791	F	MP:0002135	abnormal kidney morphology	Uggt1<em1(IMPC)Mbp>/Uggt1<+>	C57BL/6N-Uggt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461791	F	MP:0000274	enlarged heart	Uggt1<em1(IMPC)Mbp>/Uggt1<+>	C57BL/6N-Uggt1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461792	M	MP:0002574	increased vertical activity	Ugt2a1<em1(IMPC)Bay>/Ugt2a1<em1(IMPC)Bay>	C57BL/6N-Ugt2a1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6461793	F	MP:0005586	decreased tidal volume	Unc119b<tm1.1(KOMP)Vlcg>/Unc119b<tm1.1(KOMP)Vlcg>	C57BL/6N-Unc119b<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6461794	F	MP:0002092	abnormal eye morphology	Unc5cl<em1(IMPC)Mbp>/Unc5cl<em1(IMPC)Mbp>	C57BL/6NCrl-Unc5cl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461794	F	MP:0001293	anophthalmia	Unc5cl<em1(IMPC)Mbp>/Unc5cl<em1(IMPC)Mbp>	C57BL/6NCrl-Unc5cl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461794	M	MP:0002060	abnormal skin morphology	Unc5cl<em1(IMPC)Mbp>/Unc5cl<em1(IMPC)Mbp>	C57BL/6NCrl-Unc5cl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461794	M	MP:0001399	hyperactivity	Unc5cl<em1(IMPC)Mbp>/Unc5cl<em1(IMPC)Mbp>	C57BL/6NCrl-Unc5cl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461794	M	MP:0005178	increased circulating cholesterol level	Unc5cl<em1(IMPC)Mbp>/Unc5cl<em1(IMPC)Mbp>	C57BL/6NCrl-Unc5cl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461794	F	MP:0001126	abnormal ovary morphology	Unc5cl<em1(IMPC)Mbp>/Unc5cl<em1(IMPC)Mbp>	C57BL/6NCrl-Unc5cl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461794	F	MP:0001402	decreased locomotor activity	Unc5cl<em1(IMPC)Mbp>/Unc5cl<em1(IMPC)Mbp>	C57BL/6NCrl-Unc5cl<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461795	M	MP:0001417	decreased exploration in new environment	Unc80<em1(IMPC)Tcp>/Unc80<+>	C57BL/6N-Unc80<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461795	F	MP:0003020	decreased circulating chloride level	Unc80<em1(IMPC)Tcp>/Unc80<+>	C57BL/6N-Unc80<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461795	F	MP:0005634	decreased circulating sodium level	Unc80<em1(IMPC)Tcp>/Unc80<+>	C57BL/6N-Unc80<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461795	M	MP:0000702	enlarged lymph nodes	Unc80<em1(IMPC)Tcp>/Unc80<+>	C57BL/6N-Unc80<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461795	M	MP:0001258	decreased body length	Unc80<em1(IMPC)Tcp>/Unc80<+>	C57BL/6N-Unc80<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6461796	M	MP:0001415	increased exploration in new environment	Urb1<em1(IMPC)Bay>/Urb1<+>	C57BL/6N-Urb1<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6461797	M	MP:0000367	abnormal coat/ hair morphology	Utp20<em1(IMPC)J>/Utp20<+>	C57BL/6NJ-Utp20<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461798	M	MP:0004174	abnormal spine curvature	Vgll3<em1(IMPC)H>/Vgll3<em1(IMPC)H>	C57BL/6NTac-Vgll3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6461799	F	MP:0003795	abnormal bone structure	Vkorc1l1<em1(IMPC)J>/Vkorc1l1<em1(IMPC)J>	C57BL/6NJ-Vkorc1l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461799	M	MP:0000221	decreased leukocyte cell number	Vkorc1l1<em1(IMPC)J>/Vkorc1l1<em1(IMPC)J>	C57BL/6NJ-Vkorc1l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461799	M	MP:0005179	decreased circulating cholesterol level	Vkorc1l1<em1(IMPC)J>/Vkorc1l1<em1(IMPC)J>	C57BL/6NJ-Vkorc1l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461799	M	MP:0005567	decreased circulating total protein level	Vkorc1l1<em1(IMPC)J>/Vkorc1l1<em1(IMPC)J>	C57BL/6NJ-Vkorc1l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461799	M	MP:0003960	increased lean body mass	Vkorc1l1<em1(IMPC)J>/Vkorc1l1<em1(IMPC)J>	C57BL/6NJ-Vkorc1l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461799	F	MP:0010124	decreased bone mineral content	Vkorc1l1<em1(IMPC)J>/Vkorc1l1<em1(IMPC)J>	C57BL/6NJ-Vkorc1l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461799	M	MP:0005419	decreased circulating serum albumin level	Vkorc1l1<em1(IMPC)J>/Vkorc1l1<em1(IMPC)J>	C57BL/6NJ-Vkorc1l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461799	F	MP:0005278	abnormal cholesterol homeostasis	Vkorc1l1<em1(IMPC)J>/Vkorc1l1<em1(IMPC)J>	C57BL/6NJ-Vkorc1l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461800	F	MP:0000266	abnormal heart morphology	Vldlr<em1(IMPC)Mbp>/Vldlr<em1(IMPC)Mbp>	C57BL/6N-Vldlr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461800	M	MP:0001415	increased exploration in new environment	Vldlr<em1(IMPC)Mbp>/Vldlr<em1(IMPC)Mbp>	C57BL/6N-Vldlr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461800	M	MP:0020870	decreased thigmotaxis	Vldlr<em1(IMPC)Mbp>/Vldlr<em1(IMPC)Mbp>	C57BL/6N-Vldlr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461800	M	MP:0001399	hyperactivity	Vldlr<em1(IMPC)Mbp>/Vldlr<em1(IMPC)Mbp>	C57BL/6N-Vldlr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461800	M	MP:0000689	abnormal spleen morphology	Vldlr<em1(IMPC)Mbp>/Vldlr<em1(IMPC)Mbp>	C57BL/6N-Vldlr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461800	M	MP:0004924	abnormal behavior	Vldlr<em1(IMPC)Mbp>/Vldlr<em1(IMPC)Mbp>	C57BL/6N-Vldlr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461800	F	MP:0009084	blind uterus	Vldlr<em1(IMPC)Mbp>/Vldlr<em1(IMPC)Mbp>	C57BL/6N-Vldlr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461800	F	MP:0000274	enlarged heart	Vldlr<em1(IMPC)Mbp>/Vldlr<em1(IMPC)Mbp>	C57BL/6N-Vldlr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461800	M	MP:0001364	decreased anxiety-related response	Vldlr<em1(IMPC)Mbp>/Vldlr<em1(IMPC)Mbp>	C57BL/6N-Vldlr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461801	F	MP:0005567	decreased circulating total protein level	Vpreb3<em1(IMPC)Wtsi>/Vpreb3<em1(IMPC)Wtsi>	C57BL/6N-Vpreb3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461803	M	MP:0001284	absent vibrissae	Vps26c<em1(IMPC)J>/Vps26c<+>	C57BL/6NJ-Vps26c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461807	F	MP:0010053	decreased grip strength	Wdfy1<em1(IMPC)J>/Wdfy1<em1(IMPC)J>	C57BL/6NJ-Wdfy1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461808	F	MP:0004357	long tibia	Wdr4<em1(IMPC)Ics>/Wdr4<+>	C57BL/6N-Wdr4<em1(IMPC)Ics>/Ics	N	MGI:5576271
MGI:6461809	F	MP:0010507	shortened RR interval	Wdr6<em1(IMPC)J>/Wdr6<em1(IMPC)J>	C57BL/6NJ-Wdr6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461809	F	MP:0005292	improved glucose tolerance	Wdr6<em1(IMPC)J>/Wdr6<em1(IMPC)J>	C57BL/6NJ-Wdr6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461809	F	MP:0001399	hyperactivity	Wdr6<em1(IMPC)J>/Wdr6<em1(IMPC)J>	C57BL/6NJ-Wdr6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461809	F	MP:0013279	increased fasting circulating glucose level	Wdr6<em1(IMPC)J>/Wdr6<em1(IMPC)J>	C57BL/6NJ-Wdr6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461812	M	MP:0002574	increased vertical activity	Wnk2<em1Murr>/Wnk2<em1Murr>	C57BL/6NJ-Wnk2<em1Murr>/Murr	N	MGI:5576271
MGI:6461814	F	MP:0002092	abnormal eye morphology	Xpo5<em1(IMPC)Mbp>/Xpo5<+>	C57BL/6NCrl-Xpo5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461814	F	MP:0000689	abnormal spleen morphology	Xpo5<em1(IMPC)Mbp>/Xpo5<+>	C57BL/6NCrl-Xpo5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461814	F	MP:0004832	enlarged ovary	Xpo5<em1(IMPC)Mbp>/Xpo5<+>	C57BL/6NCrl-Xpo5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461814	F	MP:0001126	abnormal ovary morphology	Xpo5<em1(IMPC)Mbp>/Xpo5<+>	C57BL/6NCrl-Xpo5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461814	F	MP:0000691	enlarged spleen	Xpo5<em1(IMPC)Mbp>/Xpo5<+>	C57BL/6NCrl-Xpo5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461814	M	MP:0002060	abnormal skin morphology	Xpo5<em1(IMPC)Mbp>/Xpo5<+>	C57BL/6NCrl-Xpo5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461815	F	MP:0004924	abnormal behavior	Xylt1<em1(IMPC)J>/Xylt1<+>	C57BL/6NJ-Xylt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461815	F	MP:0020870	decreased thigmotaxis	Xylt1<em1(IMPC)J>/Xylt1<+>	C57BL/6NJ-Xylt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461817	F	MP:0000709	enlarged thymus	Ythdf3<em1(IMPC)Mbp>/Ythdf3<em1(IMPC)Mbp>	C57BL/6N-Ythdf3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461817	F	MP:0000601	small liver	Ythdf3<em1(IMPC)Mbp>/Ythdf3<em1(IMPC)Mbp>	C57BL/6N-Ythdf3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461817	F	MP:0002941	increased circulating alanine transaminase level	Ythdf3<em1(IMPC)Mbp>/Ythdf3<em1(IMPC)Mbp>	C57BL/6N-Ythdf3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461817	F	MP:0000598	abnormal liver morphology	Ythdf3<em1(IMPC)Mbp>/Ythdf3<em1(IMPC)Mbp>	C57BL/6N-Ythdf3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461817	F	MP:0000703	abnormal thymus morphology	Ythdf3<em1(IMPC)Mbp>/Ythdf3<em1(IMPC)Mbp>	C57BL/6N-Ythdf3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461818	M	MP:0002874	decreased hemoglobin content	Zc3h11a<em1(IMPC)Mbp>/Zc3h11a<+>	C57BL/6NCrl-Zc3h11a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461818	F	MP:0002941	increased circulating alanine transaminase level	Zc3h11a<em1(IMPC)Mbp>/Zc3h11a<+>	C57BL/6NCrl-Zc3h11a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461818	M	MP:0002699	abnormal vitreous body morphology	Zc3h11a<em1(IMPC)Mbp>/Zc3h11a<+>	C57BL/6NCrl-Zc3h11a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461818	F	MP:0000277	abnormal heart shape	Zc3h11a<em1(IMPC)Mbp>/Zc3h11a<+>	C57BL/6NCrl-Zc3h11a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461818	M	MP:0002075	abnormal coat/hair pigmentation	Zc3h11a<em1(IMPC)Mbp>/Zc3h11a<+>	C57BL/6NCrl-Zc3h11a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461818	F	MP:0000266	abnormal heart morphology	Zc3h11a<em1(IMPC)Mbp>/Zc3h11a<+>	C57BL/6NCrl-Zc3h11a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461818	F	MP:0000703	abnormal thymus morphology	Zc3h11a<em1(IMPC)Mbp>/Zc3h11a<+>	C57BL/6NCrl-Zc3h11a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461818	M	MP:0000208	decreased hematocrit	Zc3h11a<em1(IMPC)Mbp>/Zc3h11a<+>	C57BL/6NCrl-Zc3h11a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461818	M	MP:0002875	decreased erythrocyte cell number	Zc3h11a<em1(IMPC)Mbp>/Zc3h11a<+>	C57BL/6NCrl-Zc3h11a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461819	M	MP:0002100	abnormal tooth morphology	Zdhhc20<em1(IMPC)Hmgu>/Zdhhc20<em1(IMPC)Hmgu>	C57BL/6N-Zdhhc20<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461819	M	MP:0002111	abnormal tail morphology	Zdhhc20<em1(IMPC)Hmgu>/Zdhhc20<em1(IMPC)Hmgu>	C57BL/6N-Zdhhc20<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6461820	F	MP:0009142	decreased prepulse inhibition	Zdhhc24<tm1b(EUCOMM)Hmgu>/Zdhhc24<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zdhhc24<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6461823	M	MP:0002059	abnormal seminal vesicle morphology	Zfp236<em1(IMPC)Mbp>/Zfp236<+>	C57BL/6NCrl-Zfp236<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461823	M	MP:0003068	enlarged kidney	Zfp236<em1(IMPC)Mbp>/Zfp236<+>	C57BL/6NCrl-Zfp236<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461823	M	MP:0000277	abnormal heart shape	Zfp236<em1(IMPC)Mbp>/Zfp236<+>	C57BL/6NCrl-Zfp236<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461823	M	MP:0002631	abnormal epididymis morphology	Zfp236<em1(IMPC)Mbp>/Zfp236<+>	C57BL/6NCrl-Zfp236<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461823	M	MP:0003642	absent seminal vesicle	Zfp236<em1(IMPC)Mbp>/Zfp236<+>	C57BL/6NCrl-Zfp236<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461823	M	MP:0000538	abnormal urinary bladder morphology	Zfp236<em1(IMPC)Mbp>/Zfp236<+>	C57BL/6NCrl-Zfp236<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461823	M	MP:0002997	enlarged seminal vesicle	Zfp236<em1(IMPC)Mbp>/Zfp236<+>	C57BL/6NCrl-Zfp236<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461823	M	MP:0002135	abnormal kidney morphology	Zfp236<em1(IMPC)Mbp>/Zfp236<+>	C57BL/6NCrl-Zfp236<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461823	M	MP:0004931	enlarged epididymis	Zfp236<em1(IMPC)Mbp>/Zfp236<+>	C57BL/6NCrl-Zfp236<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461823	M	MP:0011874	enlarged urinary bladder	Zfp236<em1(IMPC)Mbp>/Zfp236<+>	C57BL/6NCrl-Zfp236<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461823	F	MP:0002188	small heart	Zfp236<em1(IMPC)Mbp>/Zfp236<+>	C57BL/6NCrl-Zfp236<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461823	F	MP:0000601	small liver	Zfp236<em1(IMPC)Mbp>/Zfp236<+>	C57BL/6NCrl-Zfp236<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461823	F	MP:0009084	blind uterus	Zfp236<em1(IMPC)Mbp>/Zfp236<+>	C57BL/6NCrl-Zfp236<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6461825	M	MP:0000689	abnormal spleen morphology	Zfp281<em1(IMPC)Mbp>/Zfp281<+>	C57BL/6N-Zfp281<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461825	F	MP:0001399	hyperactivity	Zfp281<em1(IMPC)Mbp>/Zfp281<+>	C57BL/6N-Zfp281<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461825	M	MP:0000692	small spleen	Zfp281<em1(IMPC)Mbp>/Zfp281<+>	C57BL/6N-Zfp281<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461825	F	MP:0001364	decreased anxiety-related response	Zfp281<em1(IMPC)Mbp>/Zfp281<+>	C57BL/6N-Zfp281<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461827	F	MP:0002075	abnormal coat/hair pigmentation	Zfp512<em1(IMPC)J>/Zfp512<em1(IMPC)J>	C57BL/6NJ-Zfp512<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461827	F	MP:0001529	abnormal vocalization	Zfp512<em1(IMPC)J>/Zfp512<em1(IMPC)J>	C57BL/6NJ-Zfp512<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461827	F	MP:0001399	hyperactivity	Zfp512<em1(IMPC)J>/Zfp512<em1(IMPC)J>	C57BL/6NJ-Zfp512<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461827	F	MP:0010053	decreased grip strength	Zfp512<em1(IMPC)J>/Zfp512<em1(IMPC)J>	C57BL/6NJ-Zfp512<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461828	M	MP:0005293	impaired glucose tolerance	Zfp664<tm1b(EUCOMM)Wtsi>/Zfp664<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp664<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461828	M	MP:0002968	increased circulating alkaline phosphatase level	Zfp664<tm1b(EUCOMM)Wtsi>/Zfp664<tm1b(EUCOMM)Wtsi>	C57BL/6N-Zfp664<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6461829	M	MP:0001488	increased startle reflex	Zfp69<tm1b(EUCOMM)Hmgu>/Zfp69<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp69<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6461830	F	MP:0010052	increased grip strength	Zfp711<em1(IMPC)J>/Zfp711<em1(IMPC)J>	C57BL/6NJ-Zfp711<em1(IMPC)J>/J	N	MGI:5576271
MGI:6461831	F	MP:0001392	abnormal locomotor behavior	Zfp787<em1(IMPC)J>/Zfp787<em1(IMPC)J>	C57BL/6NJ-Zfp787<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461831	F	MP:0005278	abnormal cholesterol homeostasis	Zfp787<em1(IMPC)J>/Zfp787<em1(IMPC)J>	C57BL/6NJ-Zfp787<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461831	F	MP:0005293	impaired glucose tolerance	Zfp787<em1(IMPC)J>/Zfp787<em1(IMPC)J>	C57BL/6NJ-Zfp787<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461831	F	MP:0009142	decreased prepulse inhibition	Zfp787<em1(IMPC)J>/Zfp787<em1(IMPC)J>	C57BL/6NJ-Zfp787<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461831	M	MP:0002833	increased heart weight	Zfp787<em1(IMPC)J>/Zfp787<em1(IMPC)J>	C57BL/6NJ-Zfp787<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461831	M	MP:0003179	thrombocytopenia	Zfp787<em1(IMPC)J>/Zfp787<em1(IMPC)J>	C57BL/6NJ-Zfp787<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461832	F	MP:0010052	increased grip strength	Zfp871<tm1b(EUCOMM)Wtsi>/Zfp871<+>	C57BL/6N-Zfp871<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6461832	M	MP:0010097	abnormal retina blood vessel morphology	Zfp871<tm1b(EUCOMM)Wtsi>/Zfp871<+>	C57BL/6N-Zfp871<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6461832	F	MP:0003733	abnormal retina inner nuclear layer morphology	Zfp871<tm1b(EUCOMM)Wtsi>/Zfp871<+>	C57BL/6N-Zfp871<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6461836	F	MP:0000702	enlarged lymph nodes	Zkscan7<em1(IMPC)Mbp>/Zkscan7<em1(IMPC)Mbp>	C57BL/6N-Zkscan7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461836	F	MP:0000689	abnormal spleen morphology	Zkscan7<em1(IMPC)Mbp>/Zkscan7<em1(IMPC)Mbp>	C57BL/6N-Zkscan7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461836	F	MP:0002339	abnormal lymph node morphology	Zkscan7<em1(IMPC)Mbp>/Zkscan7<em1(IMPC)Mbp>	C57BL/6N-Zkscan7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461836	F	MP:0001293	anophthalmia	Zkscan7<em1(IMPC)Mbp>/Zkscan7<em1(IMPC)Mbp>	C57BL/6N-Zkscan7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461836	F	MP:0002092	abnormal eye morphology	Zkscan7<em1(IMPC)Mbp>/Zkscan7<em1(IMPC)Mbp>	C57BL/6N-Zkscan7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461836	F	MP:0000691	enlarged spleen	Zkscan7<em1(IMPC)Mbp>/Zkscan7<em1(IMPC)Mbp>	C57BL/6N-Zkscan7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461838	M	MP:0010025	decreased total body fat amount	Znfx1<em1(IMPC)J>/Znfx1<em1(IMPC)J>	C57BL/6NJ-Znfx1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6461839	M	MP:0001552	increased circulating triglyceride level	Zranb3<em1(IMPC)Mbp>/Zranb3<em1(IMPC)Mbp>	C57BL/6N-Zranb3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461840	M	MP:0000219	increased neutrophil cell number	Zrsr2<em1(IMPC)Mbp>/Y	C57BL/6N-Zrsr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461840	M	MP:0000274	enlarged heart	Zrsr2<em1(IMPC)Mbp>/Y	C57BL/6N-Zrsr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461840	M	MP:0005016	decreased lymphocyte cell number	Zrsr2<em1(IMPC)Mbp>/Y	C57BL/6N-Zrsr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461840	M	MP:0000266	abnormal heart morphology	Zrsr2<em1(IMPC)Mbp>/Y	C57BL/6N-Zrsr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461841	F	MP:0000266	abnormal heart morphology	Zrsr2<em1(IMPC)Mbp>/Zrsr2<em1(IMPC)Mbp>	C57BL/6N-Zrsr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461841	F	MP:0000274	enlarged heart	Zrsr2<em1(IMPC)Mbp>/Zrsr2<em1(IMPC)Mbp>	C57BL/6N-Zrsr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461841	F	MP:0000601	small liver	Zrsr2<em1(IMPC)Mbp>/Zrsr2<em1(IMPC)Mbp>	C57BL/6N-Zrsr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461841	F	MP:0001926	female infertility	Zrsr2<em1(IMPC)Mbp>/Zrsr2<em1(IMPC)Mbp>	C57BL/6N-Zrsr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6461841	F	MP:0000598	abnormal liver morphology	Zrsr2<em1(IMPC)Mbp>/Zrsr2<em1(IMPC)Mbp>	C57BL/6N-Zrsr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6466594	M	MP:0008432	abnormal long-term spatial reference memory	Pak3<tm1.1Rpo>/Y	B6.129S2(Cg)-Pak3<tm1.1Rpo>	N	31943058
MGI:6466594	M	MP:0004811	abnormal neuron physiology	Pak3<tm1.1Rpo>/Y	B6.129S2(Cg)-Pak3<tm1.1Rpo>	N	31943058
MGI:6466594	M	MP:0009937	abnormal neuron differentiation	Pak3<tm1.1Rpo>/Y	B6.129S2(Cg)-Pak3<tm1.1Rpo>	N	31943058
MGI:6466594	M	MP:0020335	abnormal dentate gyrus neuron dendrite morphology	Pak3<tm1.1Rpo>/Y	B6.129S2(Cg)-Pak3<tm1.1Rpo>	N	31943058
MGI:6466594	M	MP:0002063	abnormal learning/memory/conditioning	Pak3<tm1.1Rpo>/Y	B6.129S2(Cg)-Pak3<tm1.1Rpo>	N	31943058
MGI:6466705	M	MP:0001925	male infertility	Cfap206<tm1.2Gos>/Cfap206<tm1.2Gos>	involves: 129 * C57BL/6J * CD-1 * SJL	N	32376681
MGI:6466705	M	MP:0031438	abnormal sperm radial spoke morphology	Cfap206<tm1.2Gos>/Cfap206<tm1.2Gos>	involves: 129 * C57BL/6J * CD-1 * SJL	N	32376681
MGI:6466705	F	MP:0005389	reproductive system phenotype	Cfap206<tm1.2Gos>/Cfap206<tm1.2Gos>	involves: 129 * C57BL/6J * CD-1 * SJL	Y	32376681
MGI:6466705	M	MP:0009237	kinked sperm flagellum	Cfap206<tm1.2Gos>/Cfap206<tm1.2Gos>	involves: 129 * C57BL/6J * CD-1 * SJL	N	32376681
MGI:6466705	M	MP:0002675	asthenozoospermia	Cfap206<tm1.2Gos>/Cfap206<tm1.2Gos>	involves: 129 * C57BL/6J * CD-1 * SJL	N	32376681
MGI:6466705	M	MP:0009238	coiled sperm flagellum	Cfap206<tm1.2Gos>/Cfap206<tm1.2Gos>	involves: 129 * C57BL/6J * CD-1 * SJL	N	32376681
MGI:6467361	M	MP:0009451	abnormal chromosomal synapsis	Hsf2bp<em1Roka>/Hsf2bp<em1Roka>	C57BL/6JOlaHsd-Hsf2bp<em1Roka>	N	31242413
MGI:6467361	F	MP:0005389	reproductive system phenotype	Hsf2bp<em1Roka>/Hsf2bp<em1Roka>	C57BL/6JOlaHsd-Hsf2bp<em1Roka>	Y	31242413
MGI:6467361	M	MP:0005159	azoospermia	Hsf2bp<em1Roka>/Hsf2bp<em1Roka>	C57BL/6JOlaHsd-Hsf2bp<em1Roka>	N	31242413
MGI:6467361	M	MP:0011101	prenatal lethality, incomplete penetrance	Hsf2bp<em1Roka>/Hsf2bp<em1Roka>	C57BL/6JOlaHsd-Hsf2bp<em1Roka>	N	31242413
MGI:6467361	M	MP:0005169	abnormal male meiosis	Hsf2bp<em1Roka>/Hsf2bp<em1Roka>	C57BL/6JOlaHsd-Hsf2bp<em1Roka>	N	31242413
MGI:6467361	M	MP:0006379	abnormal spermatocyte morphology	Hsf2bp<em1Roka>/Hsf2bp<em1Roka>	C57BL/6JOlaHsd-Hsf2bp<em1Roka>	N	31242413
MGI:6467361	M	MP:0001147	small testis	Hsf2bp<em1Roka>/Hsf2bp<em1Roka>	C57BL/6JOlaHsd-Hsf2bp<em1Roka>	N	31242413
MGI:6467361	M	MP:0001925	male infertility	Hsf2bp<em1Roka>/Hsf2bp<em1Roka>	C57BL/6JOlaHsd-Hsf2bp<em1Roka>	N	31242413
MGI:6467953	M	MP:0001625	cardiac hypertrophy	Tbc1d25<Gt(IST10205D5)Tigm>/Y	involves: C57BL/6N	N	32210723
MGI:6467953	M	MP:0005630	increased lung weight	Tbc1d25<Gt(IST10205D5)Tigm>/Y	involves: C57BL/6N	N	32210723
MGI:6467953	M	MP:0005598	decreased heart ventricle muscle contractility	Tbc1d25<Gt(IST10205D5)Tigm>/Y	involves: C57BL/6N	N	32210723
MGI:6467953	M	MP:0004564	increased myocardial fiber size	Tbc1d25<Gt(IST10205D5)Tigm>/Y	involves: C57BL/6N	N	32210723
MGI:6467953	M	MP:0005608	cardiac interstitial fibrosis	Tbc1d25<Gt(IST10205D5)Tigm>/Y	involves: C57BL/6N	N	32210723
MGI:6467953	M	MP:0003141	cardiac fibrosis	Tbc1d25<Gt(IST10205D5)Tigm>/Y	involves: C57BL/6N	N	32210723
MGI:6467953	M	MP:0000274	enlarged heart	Tbc1d25<Gt(IST10205D5)Tigm>/Y	involves: C57BL/6N	N	32210723
MGI:6467953	M	MP:0002833	increased heart weight	Tbc1d25<Gt(IST10205D5)Tigm>/Y	involves: C57BL/6N	N	32210723
MGI:6467953	M	MP:0005140	decreased cardiac muscle contractility	Tbc1d25<Gt(IST10205D5)Tigm>/Y	involves: C57BL/6N	N	32210723
MGI:6467953	M	MP:0004485	increased response of heart to induced stress	Tbc1d25<Gt(IST10205D5)Tigm>/Y	involves: C57BL/6N	N	32210723
MGI:6468047	M	MP:0014052	increased male germ cell apoptosis	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0020849	abnormal actin cytoskeleton morphology	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0009325	necrospermia	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0002687	oligozoospermia	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0008839	absent acrosome	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0030980	abnormal acroplaxome morphology	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0005578	teratozoospermia	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0009232	abnormal sperm nucleus morphology	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0005384	cellular phenotype	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	Y	31218450
MGI:6468047	M	MP:0001147	small testis	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0002686	globozoospermia	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0011743	abnormal Golgi apparatus morphology	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0020550	multinucleated giant male germ cells	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0001925	male infertility	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0030949	abnormal Golgi vesicle transport	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468047	M	MP:0030952	abnormal Golgi stack morphology	Vps13b<tm1.2Ics>/Vps13b<tm1.2Ics>	involves: C57BL/6N	N	31218450
MGI:6468250	M	MP:0002919	enhanced paired-pulse facilitation	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0002064	seizures	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0008414	abnormal spatial reference memory	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0001441	increased grooming behavior	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0009456	impaired cued conditioning behavior	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0008432	abnormal long-term spatial reference memory	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0000418	focal hair loss	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0020514	abnormal dendritic thin spine morphology	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0020513	abnormal dendritic stubby spine morphology	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0020510	increased dendritic spine length	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0020508	decreased dendritic spine density	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0002083	premature death	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0004924	abnormal behavior	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0009454	impaired contextual conditioning behavior	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0020395	abnormal response to social novelty	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0003107	abnormal response to novelty	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0013117	focal hair loss in thorax region	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0001363	increased anxiety-related response	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0031391	increased locomotor activity	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0001409	increased stereotypic behavior	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0002206	abnormal CNS synaptic transmission	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0004998	decreased CNS synapse formation	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0001360	abnormal social investigation	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0001529	abnormal vocalization	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0020351	decreased vocalization	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468250	M	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology	Nexmif<tm1(KOMP)Wtsi>/Y	B6J.B6N-Nexmif<tm1(KOMP)Wtsi>	N	31704787
MGI:6468346	M	MP:0005159	azoospermia	Spocd1<em1Doca>/Spocd1<em1Doca>	involves: C57BL/6 * C57BL/6N * CBA	N	32674113
MGI:6468346	M	MP:0001925	male infertility	Spocd1<em1Doca>/Spocd1<em1Doca>	involves: C57BL/6 * C57BL/6N * CBA	N	32674113
MGI:6468346	M	MP:0013601	increased testis apoptosis	Spocd1<em1Doca>/Spocd1<em1Doca>	involves: C57BL/6 * C57BL/6N * CBA	N	32674113
MGI:6468346	M	MP:0008878	abnormal DNA methylation during gametogenesis	Spocd1<em1Doca>/Spocd1<em1Doca>	involves: C57BL/6 * C57BL/6N * CBA	N	32674113
MGI:6468346	M	MP:0002216	abnormal seminiferous tubule morphology	Spocd1<em1Doca>/Spocd1<em1Doca>	involves: C57BL/6 * C57BL/6N * CBA	N	32674113
MGI:6468346	M	MP:0003205	testicular atrophy	Spocd1<em1Doca>/Spocd1<em1Doca>	involves: C57BL/6 * C57BL/6N * CBA	N	32674113
MGI:6468346	M	MP:0013600	testis degeneration	Spocd1<em1Doca>/Spocd1<em1Doca>	involves: C57BL/6 * C57BL/6N * CBA	N	32674113
MGI:6468346	M	MP:0009451	abnormal chromosomal synapsis	Spocd1<em1Doca>/Spocd1<em1Doca>	involves: C57BL/6 * C57BL/6N * CBA	N	32674113
MGI:6469466	M	MP:0001922	reduced male fertility	Cfap97d1<em1Osb>/Cfap97d1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32785227
MGI:6469466	M	MP:0002675	asthenozoospermia	Cfap97d1<em1Osb>/Cfap97d1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32785227
MGI:6469466	M	MP:0030976	impaired sperm penetration of zona pellucida	Cfap97d1<em1Osb>/Cfap97d1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32785227
MGI:6469466	F	MP:0005389	reproductive system phenotype	Cfap97d1<em1Osb>/Cfap97d1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32785227
MGI:6469466	M	MP:0009838	abnormal sperm axoneme morphology	Cfap97d1<em1Osb>/Cfap97d1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32785227
MGI:6469467	M	MP:0002675	asthenozoospermia	Cfap97d1<tm1a(KOMP)Wtsi>/Cfap97d1<tm1a(KOMP)Wtsi>	involves: 129S/SvEv * C57BL/6N	N	32785227
MGI:6469467	F	MP:0005389	reproductive system phenotype	Cfap97d1<tm1a(KOMP)Wtsi>/Cfap97d1<tm1a(KOMP)Wtsi>	involves: 129S/SvEv * C57BL/6N	Y	32785227
MGI:6469467	M	MP:0001922	reduced male fertility	Cfap97d1<tm1a(KOMP)Wtsi>/Cfap97d1<tm1a(KOMP)Wtsi>	involves: 129S/SvEv * C57BL/6N	N	32785227
MGI:6469467	M	MP:0030976	impaired sperm penetration of zona pellucida	Cfap97d1<tm1a(KOMP)Wtsi>/Cfap97d1<tm1a(KOMP)Wtsi>	involves: 129S/SvEv * C57BL/6N	N	32785227
MGI:6469632	M	MP:0002161	abnormal fertility/fecundity	Zbed3<tm1.1Lil>/Zbed3<tm1.1Lil>	Not Specified	N	28992324
MGI:6469632	F	MP:0001935	decreased litter size	Zbed3<tm1.1Lil>/Zbed3<tm1.1Lil>	Not Specified	N	28992324
MGI:6469632	F	MP:0003718	maternal effect	Zbed3<tm1.1Lil>/Zbed3<tm1.1Lil>	Not Specified	N	28992324
MGI:6469924	M	MP:0000428	abnormal craniofacial morphology	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	N	31634484
MGI:6469924	M	MP:0005608	cardiac interstitial fibrosis	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	N	31634484
MGI:6469924	M	MP:0011703	increased fibroblast proliferation	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	N	31634484
MGI:6469924	M	MP:0011708	decreased fibroblast cell migration	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	N	31634484
MGI:6469924	M	MP:0005386	behavior/neurological phenotype	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	Y	31634484
MGI:6469924	M	MP:0003821	decreased left ventricle diastolic pressure	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	N	31634484
MGI:6469924	M	MP:0003402	decreased liver weight	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	N	31634484
MGI:6469924	M	MP:0005385	cardiovascular system phenotype	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	Y	31634484
MGI:6469924	M	MP:0003918	decreased kidney weight	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	N	31634484
MGI:6469924	M	MP:0002188	small heart	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	N	31634484
MGI:6469924	M	MP:0002834	decreased heart weight	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	N	31634484
MGI:6469924	M	MP:0001262	decreased body weight	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	N	31634484
MGI:6469924	M	MP:0005376	homeostasis/metabolism phenotype	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	Y	31634484
MGI:6469924	M	MP:0008770	decreased survivor rate	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	N	31634484
MGI:6469924	M	MP:0011110	preweaning lethality, incomplete penetrance	Nono<Gt(YHA266)Byg>/Y	involves: 129P2/OlaHsd	N	31634484
MGI:6470478	M	MP:0001405	impaired coordination	Pycr2<tm1.1Brre>/Pycr2<tm1.1Brre>	involves: C57BL/6	N	32330411
MGI:6470478	M	MP:0000781	decreased corpus callosum size	Pycr2<tm1.1Brre>/Pycr2<tm1.1Brre>	involves: C57BL/6	N	32330411
MGI:6470478	M	MP:0001525	impaired balance	Pycr2<tm1.1Brre>/Pycr2<tm1.1Brre>	involves: C57BL/6	N	32330411
MGI:6470478	M	MP:0001513	limb grasping	Pycr2<tm1.1Brre>/Pycr2<tm1.1Brre>	involves: C57BL/6	N	32330411
MGI:6470478	M	MP:0001263	weight loss	Pycr2<tm1.1Brre>/Pycr2<tm1.1Brre>	involves: C57BL/6	N	32330411
MGI:6470478	M	MP:0006086	decreased body mass index	Pycr2<tm1.1Brre>/Pycr2<tm1.1Brre>	involves: C57BL/6	N	32330411
MGI:6470480	M	MP:0001513	limb grasping	Pycr2<tm2Brre>/?	involves: C57BL/6	N	32330411
MGI:6470482	M	MP:0020086	abnormal susceptibility to non-insulin-dependent diabetes	Tg(Nphs1-ACE2)#Kdbu/0	FVB//N-Tg(Nphs1-ACE2)#Kdbu	N	22475818
MGI:6470482	M	MP:0001262	decreased body weight	Tg(Nphs1-ACE2)#Kdbu/0	FVB//N-Tg(Nphs1-ACE2)#Kdbu	N	22475818
MGI:6470482	M	MP:0011753	decreased podocyte number	Tg(Nphs1-ACE2)#Kdbu/0	FVB//N-Tg(Nphs1-ACE2)#Kdbu	N	22475818
MGI:6470482	M	MP:0002644	decreased circulating triglyceride level	Tg(Nphs1-ACE2)#Kdbu/0	FVB//N-Tg(Nphs1-ACE2)#Kdbu	N	22475818
MGI:6470632	M	MP:0002662	abnormal cauda epididymis morphology	Gkap1<em1Feis>/Gkap1<em1Feis>	involves: C57BL/6	N	31318116
MGI:6470632	M	MP:0005378	growth/size/body region phenotype	Gkap1<em1Feis>/Gkap1<em1Feis>	involves: C57BL/6	Y	31318116
MGI:6470632	M	MP:0006379	abnormal spermatocyte morphology	Gkap1<em1Feis>/Gkap1<em1Feis>	involves: C57BL/6	N	31318116
MGI:6470632	M	MP:0005389	reproductive system phenotype	Gkap1<em1Feis>/Gkap1<em1Feis>	involves: C57BL/6	Y	31318116
MGI:6470632	M	MP:0001146	abnormal testis morphology	Gkap1<em1Feis>/Gkap1<em1Feis>	involves: C57BL/6	Y	31318116
MGI:6470632	M	MP:0004928	increased epididymis weight	Gkap1<em1Feis>/Gkap1<em1Feis>	involves: C57BL/6	N	31318116
MGI:6470632	M	MP:0009256	enlarged corpus epididymis	Gkap1<em1Feis>/Gkap1<em1Feis>	involves: C57BL/6	N	31318116
MGI:6470632	M	MP:0004931	enlarged epididymis	Gkap1<em1Feis>/Gkap1<em1Feis>	involves: C57BL/6	N	31318116
MGI:6470632	M	MP:0004851	increased testis weight	Gkap1<em1Feis>/Gkap1<em1Feis>	involves: C57BL/6	N	31318116
MGI:6470632	M	MP:0030603	increased sperm number	Gkap1<em1Feis>/Gkap1<em1Feis>	involves: C57BL/6	N	31318116
MGI:6470967	M	MP:0004921	decreased placenta weight	Prl7d1<em1Liga>/Prl7d1<em1Liga>	involves: C57BL/6	N	31012985
MGI:6470967	M	MP:0012108	increased trophoblast glycogen cell number	Prl7d1<em1Liga>/Prl7d1<em1Liga>	involves: C57BL/6	N	31012985
MGI:6470967	F	MP:0012726	abnormal uterine spiral artery morphology	Prl7d1<em1Liga>/Prl7d1<em1Liga>	involves: C57BL/6	N	31012985
MGI:6471015	M	MP:0001262	decreased body weight	Abhd11<tm1Esco>/Abhd11<tm1Esco>	involves: C57BL/6	N	32579589
MGI:6471015	M	MP:0009287	decreased abdominal fat pad weight	Abhd11<tm1Esco>/Abhd11<tm1Esco>	involves: C57BL/6	N	32579589
MGI:6472629	M	MP:0009454	impaired contextual conditioning behavior	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0002083	premature death	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0001405	impaired coordination	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0002064	seizures	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0001402	decreased locomotor activity	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0009456	impaired cued conditioning behavior	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0001951	abnormal breathing pattern	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0004924	abnormal behavior	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0002804	abnormal motor learning	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0001957	apnea	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0009358	environmentally induced seizures	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0020870	decreased thigmotaxis	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0001406	abnormal gait	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0005573	increased pulmonary respiratory rate	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472629	M	MP:0001407	short stride length	Mecp2<em1Jlzn>/Y	C57BL/6-Mecp2<em1Jlzn>	N	32469049
MGI:6472861	F	MP:0001273	decreased metastatic potential	Kars1<Gt(AJ0130)Wtsi>/Kars1<+>,Tg(MMTV-PyVT)634Mul/0	involves: 129P2/OlaHsd * FVB/N	N	26091349
MGI:6472874	F	MP:0012008	delayed parturition	Dux<em1Ditr>/Dux<em1Ditr>	involves: C57BL/6 * DBA/2	N	31806660
MGI:6472890	M	MP:0001925	male infertility	Adad2<em3(IMPC)J>/Adad2<em3(IMPC)J>	involves: C57BL/6NJ	N	32665638
MGI:6472890	M	MP:0005159	azoospermia	Adad2<em3(IMPC)J>/Adad2<em3(IMPC)J>	involves: C57BL/6NJ	N	32665638
MGI:6472890	M	MP:0006380	abnormal spermatid morphology	Adad2<em3(IMPC)J>/Adad2<em3(IMPC)J>	involves: C57BL/6NJ	N	32665638
MGI:6472958	M	MP:0006272	abnormal urine organic anion level	Prodh2<em1Jkni>/Prodh2<em1Jkni>	involves: C57BL/6J	N	31821850
MGI:6472958	M	MP:0009643	abnormal urine homeostasis	Prodh2<em1Jkni>/Prodh2<em1Jkni>	involves: C57BL/6J	N	31821850
MGI:6472965	M	MP:0008873	increased physiological sensitivity to xenobiotic	Grhpr<Gt(OST383093)Lex>/Grhpr<Gt(OST383093)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	N	31821850
MGI:6473220	M	MP:0012307	impaired spatial learning	Slc16a7<tm1.1Lupel>/Slc16a7<tm1.1Lupel>	C57BL/6J-Slc16a7<tm1.1Lupel>	N	32693190
MGI:6473220	M	MP:0014367	impaired long-term object recognition memory	Slc16a7<tm1.1Lupel>/Slc16a7<tm1.1Lupel>	C57BL/6J-Slc16a7<tm1.1Lupel>	N	32693190
MGI:6473220	M	MP:0005386	behavior/neurological phenotype	Slc16a7<tm1.1Lupel>/Slc16a7<tm1.1Lupel>	C57BL/6J-Slc16a7<tm1.1Lupel>	Y	32693190
MGI:6473220	M	MP:0001458	abnormal object recognition memory	Slc16a7<tm1.1Lupel>/Slc16a7<tm1.1Lupel>	C57BL/6J-Slc16a7<tm1.1Lupel>	N	32693190
MGI:6473220	M	MP:0011827	impaired neuron differentiation	Slc16a7<tm1.1Lupel>/Slc16a7<tm1.1Lupel>	C57BL/6J-Slc16a7<tm1.1Lupel>	N	32693190
MGI:6473220	M	MP:0014064	argyrophilic inclusion bodies	Slc16a7<tm1.1Lupel>/Slc16a7<tm1.1Lupel>	C57BL/6J-Slc16a7<tm1.1Lupel>	N	32693190
MGI:6473221	M	MP:0003631	nervous system phenotype	Slc16a3<tm1.1Lupel>/Slc16a3<tm1.1Lupel>	C57BL/6J-Slc16a3<tm1.1Lupel>	Y	32693190
MGI:6473221	M	MP:0014367	impaired long-term object recognition memory	Slc16a3<tm1.1Lupel>/Slc16a3<tm1.1Lupel>	C57BL/6J-Slc16a3<tm1.1Lupel>	N	32693190
MGI:6473221	M	MP:0012307	impaired spatial learning	Slc16a3<tm1.1Lupel>/Slc16a3<tm1.1Lupel>	C57BL/6J-Slc16a3<tm1.1Lupel>	N	32693190
MGI:6473221	M	MP:0005386	behavior/neurological phenotype	Slc16a3<tm1.1Lupel>/Slc16a3<tm1.1Lupel>	C57BL/6J-Slc16a3<tm1.1Lupel>	Y	32693190
MGI:6473221	M	MP:0001458	abnormal object recognition memory	Slc16a3<tm1.1Lupel>/Slc16a3<tm1.1Lupel>	C57BL/6J-Slc16a3<tm1.1Lupel>	N	32693190
MGI:6473301	M	MP:0005378	growth/size/body region phenotype	1700013H16Rik<em11Juhu>/Y	C57BL/6-1700013H16Rik<em11Juhu>	Y	26599493
MGI:6473303	F	MP:0005389	reproductive system phenotype	1700013H16Rik<em11Juhu>/1700013H16Rik<em11Juhu>	C57BL/6-1700013H16Rik<em11Juhu>	Y	26599493
MGI:6473306	M	MP:0005389	reproductive system phenotype	1700013H16Rik<em1Juhu>/Y	C57BL/6-1700013H16Rik<em1Juhu>	Y	26599493
MGI:6473306	M	MP:0005378	growth/size/body region phenotype	1700013H16Rik<em1Juhu>/Y	C57BL/6-1700013H16Rik<em1Juhu>	Y	26599493
MGI:6473307	F	MP:0005389	reproductive system phenotype	1700013H16Rik<em1Juhu>/1700013H16Rik<em1Juhu>	C57BL/6-1700013H16Rik<em1Juhu>	Y	26599493
MGI:6473313	M	MP:0000559	abnormal femur morphology	Bbln<tm1(KOMP)Wtsi>/Bbln<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	32569872
MGI:6473313	M	MP:0010879	decreased trabecular bone volume	Bbln<tm1(KOMP)Wtsi>/Bbln<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	32569872
MGI:6473313	M	MP:0004984	increased osteoclast cell number	Bbln<tm1(KOMP)Wtsi>/Bbln<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	32569872
MGI:6473313	M	MP:0010869	decreased bone trabecula number	Bbln<tm1(KOMP)Wtsi>/Bbln<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	32569872
MGI:6473313	M	MP:0005390	skeleton phenotype	Bbln<tm1(KOMP)Wtsi>/Bbln<tm1(KOMP)Wtsi>	involves: C57BL/6N	Y	32569872
MGI:6473313	M	MP:0004992	increased bone resorption	Bbln<tm1(KOMP)Wtsi>/Bbln<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	32569872
MGI:6473313	M	MP:0008396	abnormal osteoclast differentiation	Bbln<tm1(KOMP)Wtsi>/Bbln<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	32569872
MGI:6473316	M	MP:0008396	abnormal osteoclast differentiation	Bbln<tm1(KOMP)Wtsi>/Bbln<+>	involves: C57BL/6N	N	32569872
MGI:6473340	F	MP:0001923	reduced female fertility	Del(XJpx-Ftx)1Ehea/+	involves: C57BL/6 * DBA/2	N	32238933
MGI:6473342	F	MP:0005389	reproductive system phenotype	Jpx<em1Ehea>/Jpx<+>	involves: C57BL/6 * DBA/2	Y	32238933
MGI:6473561	M	MP:0004274	abnormal embryonic/fetal subventricular zone morphology	Eml1<tm1.2Ics>/Eml1<+>	C57BL/6N-Eml1<tm1.2Ics>	N	31173351
MGI:6473561	M	MP:0008439	abnormal cortical plate morphology	Eml1<tm1.2Ics>/Eml1<+>	C57BL/6N-Eml1<tm1.2Ics>	N	31173351
MGI:6473655	M	MP:0003058	increased insulin secretion	Sphkap<tm1.1Nina>/Sphkap<tm1.1Nina>	Not Specified	N	28396589
MGI:6473655	M	MP:0002727	decreased circulating insulin level	Sphkap<tm1.1Nina>/Sphkap<tm1.1Nina>	Not Specified	N	28396589
MGI:6473655	M	MP:0005560	decreased circulating glucose level	Sphkap<tm1.1Nina>/Sphkap<tm1.1Nina>	Not Specified	N	28396589
MGI:6473655	M	MP:0002079	increased circulating insulin level	Sphkap<tm1.1Nina>/Sphkap<tm1.1Nina>	Not Specified	N	28396589
MGI:6473655	M	MP:0003059	decreased insulin secretion	Sphkap<tm1.1Nina>/Sphkap<tm1.1Nina>	Not Specified	N	28396589
MGI:6473661	M	MP:0002083	premature death	Gt(ROSA)26Sor<tm1(CAG-SNCA)Tanj>/Gt(ROSA)26Sor<tm1(CAG-SNCA)Tanj>,Tg(Plp1-cre/ERT)3Pop/0	involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl * DBA/2	N	30910745
MGI:6473854	M	MP:0004984	increased osteoclast cell number	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0010869	decreased bone trabecula number	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0010879	decreased trabecular bone volume	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0004214	abnormal long bone diaphysis morphology	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0030985	decreased circulating osteocalcin level	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0008152	decreased diameter of femur	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0008553	increased circulating tumor necrosis factor level	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0030439	decreased osteoblast proliferation	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0008638	increased circulating interleukin-1 alpha level	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0031074	increased circulating type I collagen C-terminal telopeptide level	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0008713	abnormal cytokine level	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0008596	increased circulating interleukin-6 level	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0008593	increased circulating interleukin-10 level	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0001541	abnormal osteoclast physiology	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0013630	increased bone trabecular spacing	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0009346	decreased trabecular bone thickness	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473854	M	MP:0000066	osteoporosis	Itln1<em1Cya>/Itln1<em1Cya>	involves: C57BL/6	N	29619269
MGI:6473984	M	MP:0008545	absent sperm flagellum	Dnah8<em1Osb>/Dnah8<em1Osb>	involves: C57BL/6 * DBA/2	N	32619401
MGI:6473984	M	MP:0014468	disorganized sperm mitochondrial sheath	Dnah8<em1Osb>/Dnah8<em1Osb>	involves: C57BL/6 * DBA/2	N	32619401
MGI:6473984	M	MP:0009239	short sperm flagellum	Dnah8<em1Osb>/Dnah8<em1Osb>	involves: C57BL/6 * DBA/2	N	32619401
MGI:6473984	M	MP:0020869	immotile sperm	Dnah8<em1Osb>/Dnah8<em1Osb>	involves: C57BL/6 * DBA/2	N	32619401
MGI:6473984	M	MP:0009238	coiled sperm flagellum	Dnah8<em1Osb>/Dnah8<em1Osb>	involves: C57BL/6 * DBA/2	N	32619401
MGI:6473984	M	MP:0009237	kinked sperm flagellum	Dnah8<em1Osb>/Dnah8<em1Osb>	involves: C57BL/6 * DBA/2	N	32619401
MGI:6473984	M	MP:0001156	abnormal spermatogenesis	Dnah8<em1Osb>/Dnah8<em1Osb>	involves: C57BL/6 * DBA/2	N	32619401
MGI:6473984	M	MP:0008892	abnormal sperm flagellum morphology	Dnah8<em1Osb>/Dnah8<em1Osb>	involves: C57BL/6 * DBA/2	N	32619401
MGI:6473984	M	MP:0031356	abnormal outer dense fiber morphology	Dnah8<em1Osb>/Dnah8<em1Osb>	involves: C57BL/6 * DBA/2	N	32619401
MGI:6473984	M	MP:0001925	male infertility	Dnah8<em1Osb>/Dnah8<em1Osb>	involves: C57BL/6 * DBA/2	N	32619401
MGI:6473984	M	MP:0030590	abnormal sperm fibrous sheath morphology	Dnah8<em1Osb>/Dnah8<em1Osb>	involves: C57BL/6 * DBA/2	N	32619401
MGI:6473984	M	MP:0009838	abnormal sperm axoneme morphology	Dnah8<em1Osb>/Dnah8<em1Osb>	involves: C57BL/6 * DBA/2	N	32619401
MGI:6474216	M	MP:0000774	decreased brain size	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474216	M	MP:0006254	thin cerebral cortex	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474216	M	MP:0000812	abnormal dentate gyrus morphology	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474216	M	MP:0002175	decreased brain weight	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474216	M	MP:0009456	impaired cued conditioning behavior	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474216	M	MP:0004045	abnormal cell cycle checkpoint function	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474216	M	MP:0012203	abnormal neuronal stem cell morphology	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474216	M	MP:0004046	abnormal mitosis	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474216	M	MP:0000433	microcephaly	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474216	M	MP:0008263	abnormal hippocampus CA1 region morphology	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474216	M	MP:0008284	abnormal hippocampus pyramidal cell layer	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474216	M	MP:0003077	abnormal cell cycle	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474216	M	MP:0001525	impaired balance	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474216	M	MP:0003631	nervous system phenotype	Pqbp1<tm1.1Hiok>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	Y	25070536
MGI:6474219	F	MP:0000774	decreased brain size	Pqbp1<tm1.1Hiok>/Pqbp1<+>,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474221	M	MP:0003631	nervous system phenotype	Pqbp1<tm1.1Hiok>/Y,Tg(Syn1-cre)671Jxm/0	involves: C57BL/6 * C57BL/6J	Y	25070536
MGI:6474221	M	MP:0002882	abnormal neuron morphology	Pqbp1<tm1.1Hiok>/Y,Tg(Syn1-cre)671Jxm/0	involves: C57BL/6 * C57BL/6J	N	25070536
MGI:6474227	M	MP:0001402	decreased locomotor activity	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6474227	M	MP:0003172	abnormal lysosome physiology	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6474227	M	MP:0030808	abnormal hindlimb joint morphology	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6474227	M	MP:0030074	coarse facial features	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6474227	M	MP:0009840	abnormal foam cell morphology	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6474227	M	MP:0003743	abnormal facial morphology	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6474227	M	MP:0001259	abnormal body weight	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6474227	M	MP:0030811	abnormal hand joint morphology	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6474227	M	MP:0002083	premature death	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6474227	M	MP:0030068	large face	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6474227	M	MP:0000414	alopecia	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6474227	M	MP:0011473	increased urine glycosaminoglycan level	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6474227	M	MP:0011475	abnormal glycosaminoglycan level	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6474227	M	MP:0000443	abnormal snout morphology	Ids<tm1Dkji>/Y	involves: C57BL/6	N	20652491
MGI:6476690	M	MP:0001399	hyperactivity	Synm<tm1.1Ics>/Synm<tm1.1Ics>	involves: 129S2/SvPas * C57BL/6 * FVB/N * SJL	N	25179606
MGI:6476690	M	MP:0008965	increased basal metabolism	Synm<tm1.1Ics>/Synm<tm1.1Ics>	involves: 129S2/SvPas * C57BL/6 * FVB/N * SJL	N	25179606
MGI:6476690	M	MP:0001257	increased body length	Synm<tm1.1Ics>/Synm<tm1.1Ics>	involves: 129S2/SvPas * C57BL/6 * FVB/N * SJL	N	25179606
MGI:6476690	M	MP:0011941	increased fluid intake	Synm<tm1.1Ics>/Synm<tm1.1Ics>	involves: 129S2/SvPas * C57BL/6 * FVB/N * SJL	N	25179606
MGI:6476690	M	MP:0004357	long tibia	Synm<tm1.1Ics>/Synm<tm1.1Ics>	involves: 129S2/SvPas * C57BL/6 * FVB/N * SJL	N	25179606
MGI:6476690	M	MP:0003960	increased lean body mass	Synm<tm1.1Ics>/Synm<tm1.1Ics>	involves: 129S2/SvPas * C57BL/6 * FVB/N * SJL	N	25179606
MGI:6476690	M	MP:0005289	increased oxygen consumption	Synm<tm1.1Ics>/Synm<tm1.1Ics>	involves: 129S2/SvPas * C57BL/6 * FVB/N * SJL	N	25179606
MGI:6476699	M	MP:0030410	middle ear effusion	Ids<tm1Dkji>/Y	involves: 129 * C57BL/6	N	22847837
MGI:6476699	M	MP:0006021	abnormal Reissner membrane morphology	Ids<tm1Dkji>/Y	involves: 129 * C57BL/6	N	22847837
MGI:6476699	M	MP:0006018	abnormal tympanic membrane morphology	Ids<tm1Dkji>/Y	involves: 129 * C57BL/6	N	22847837
MGI:6476699	M	MP:0004288	abnormal spiral ligament morphology	Ids<tm1Dkji>/Y	involves: 129 * C57BL/6	N	22847837
MGI:6476699	M	MP:0004308	abnormal basilar membrane morphology	Ids<tm1Dkji>/Y	involves: 129 * C57BL/6	N	22847837
MGI:6476699	M	MP:0011967	increased or absent threshold for auditory brainstem response	Ids<tm1Dkji>/Y	involves: 129 * C57BL/6	N	22847837
MGI:6476699	M	MP:0011475	abnormal glycosaminoglycan level	Ids<tm1Dkji>/Y	involves: 129 * C57BL/6	N	22847837
MGI:6476699	M	MP:0002855	abnormal cochlear ganglion morphology	Ids<tm1Dkji>/Y	involves: 129 * C57BL/6	N	22847837
MGI:6476699	M	MP:0003172	abnormal lysosome physiology	Ids<tm1Dkji>/Y	involves: 129 * C57BL/6	N	22847837
MGI:6477002	M	MP:0005389	reproductive system phenotype	Lrrc34<em1Doson>/Lrrc34<em1Doson>	involves: C57BL/6 * DBA/2J	Y	31621016
MGI:6477029	M	MP:0003896	prolonged PR interval	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0031302	syncope	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0003233	prolonged QT interval	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0011919	abnormal R wave	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0002083	premature death	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0010392	prolonged QRS complex duration	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0006110	ventricular fibrillation	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0011925	abnormal heart echocardiography feature	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0008543	atrial fibrillation	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0005140	decreased cardiac muscle contractility	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0002795	dilated cardiomyopathy	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0000280	thin ventricular wall	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0008950	ventricular tachycardia	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0003141	cardiac fibrosis	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0004071	prolonged P wave	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477029	M	MP:0000274	enlarged heart	Rbm20<em1Hide>/Rbm20<em1Hide>	involves: C57BL/6J	N	33110103
MGI:6477030	M	MP:0011925	abnormal heart echocardiography feature	Rbm20<em1Hide>/Rbm20<+>	involves: C57BL/6J	N	33110103
MGI:6477030	M	MP:0005140	decreased cardiac muscle contractility	Rbm20<em1Hide>/Rbm20<+>	involves: C57BL/6J	N	33110103
MGI:6477030	M	MP:0008543	atrial fibrillation	Rbm20<em1Hide>/Rbm20<+>	involves: C57BL/6J	N	33110103
MGI:6477031	M	MP:0008543	atrial fibrillation	Rbm20<em3Hide>/Rbm20<em3Hide>	involves: C57BL/6J	N	33110103
MGI:6477031	M	MP:0005140	decreased cardiac muscle contractility	Rbm20<em3Hide>/Rbm20<em3Hide>	involves: C57BL/6J	N	33110103
MGI:6477031	M	MP:0003233	prolonged QT interval	Rbm20<em3Hide>/Rbm20<em3Hide>	involves: C57BL/6J	N	33110103
MGI:6477031	M	MP:0011925	abnormal heart echocardiography feature	Rbm20<em3Hide>/Rbm20<em3Hide>	involves: C57BL/6J	N	33110103
MGI:6477264	F	MP:0008770	decreased survivor rate	Zc4h2<em1.1Yqd>/Zc4h2<+>	involves: C57BL/6 * FVB	N	31336385
MGI:6477264	F	MP:0000955	abnormal spinal cord morphology	Zc4h2<em1.1Yqd>/Zc4h2<+>	involves: C57BL/6 * FVB	N	31336385
MGI:6477264	F	MP:0001732	postnatal growth retardation	Zc4h2<em1.1Yqd>/Zc4h2<+>	involves: C57BL/6 * FVB	N	31336385
MGI:6477264	F	MP:0002083	premature death	Zc4h2<em1.1Yqd>/Zc4h2<+>	involves: C57BL/6 * FVB	N	31336385
MGI:6477265	M	MP:0011087	neonatal lethality, complete penetrance	Zc4h2<em1.1Yqd>/Y	involves: C57BL/6 * FVB	N	31336385
MGI:6477265	M	MP:0000955	abnormal spinal cord morphology	Zc4h2<em1.1Yqd>/Y	involves: C57BL/6 * FVB	N	31336385
MGI:6477265	M	MP:0000939	decreased motor neuron number	Zc4h2<em1.1Yqd>/Y	involves: C57BL/6 * FVB	N	31336385
MGI:6477265	M	MP:0005390	skeleton phenotype	Zc4h2<em1.1Yqd>/Y	involves: C57BL/6 * FVB	Y	31336385
MGI:6477265	M	MP:0004100	abnormal spinal cord interneuron morphology	Zc4h2<em1.1Yqd>/Y	involves: C57BL/6 * FVB	N	31336385
MGI:6477266	F	MP:0000939	decreased motor neuron number	Zc4h2<em1.1Yqd>/Zc4h2<em1.1Yqd>	involves: C57BL/6 * FVB	N	31336385
MGI:6477266	F	MP:0021101	abnormal ventral interneuron morphology	Zc4h2<em1.1Yqd>/Zc4h2<em1.1Yqd>	involves: C57BL/6 * FVB	N	31336385
MGI:6477266	F	MP:0011087	neonatal lethality, complete penetrance	Zc4h2<em1.1Yqd>/Zc4h2<em1.1Yqd>	involves: C57BL/6 * FVB	N	31336385
MGI:6477266	F	MP:0005390	skeleton phenotype	Zc4h2<em1.1Yqd>/Zc4h2<em1.1Yqd>	involves: C57BL/6 * FVB	Y	31336385
MGI:6477266	F	MP:0000955	abnormal spinal cord morphology	Zc4h2<em1.1Yqd>/Zc4h2<em1.1Yqd>	involves: C57BL/6 * FVB	N	31336385
MGI:6477388	F	MP:0005343	increased circulating aspartate transaminase level	Fam3a<em1Cya>/Fam3a<em1Cya>	involves: C57BL/6	N	28562339
MGI:6477388	F	MP:0003957	abnormal nitric oxide homeostasis	Fam3a<em1Cya>/Fam3a<em1Cya>	involves: C57BL/6	N	28562339
MGI:6477388	F	MP:0005425	increased macrophage cell number	Fam3a<em1Cya>/Fam3a<em1Cya>	involves: C57BL/6	N	28562339
MGI:6477388	F	MP:0009763	increased susceptibility to induced morbidity/mortality	Fam3a<em1Cya>/Fam3a<em1Cya>	involves: C57BL/6	N	28562339
MGI:6477388	F	MP:0011009	increased circulating glutamate dehydrogenase level	Fam3a<em1Cya>/Fam3a<em1Cya>	involves: C57BL/6	N	28562339
MGI:6477388	F	MP:0005376	homeostasis/metabolism phenotype	Fam3a<em1Cya>/Fam3a<em1Cya>	involves: C57BL/6	Y	32312868
MGI:6477388	F	MP:0008039	increased NK T cell number	Fam3a<em1Cya>/Fam3a<em1Cya>	involves: C57BL/6	N	28562339
MGI:6477388	F	MP:0005015	increased T cell number	Fam3a<em1Cya>/Fam3a<em1Cya>	involves: C57BL/6	N	28562339
MGI:6477388	F	MP:0012659	decreased superoxide dismutase level	Fam3a<em1Cya>/Fam3a<em1Cya>	involves: C57BL/6	N	28562339
MGI:6477388	F	MP:0002941	increased circulating alanine transaminase level	Fam3a<em1Cya>/Fam3a<em1Cya>	involves: C57BL/6	N	28562339
MGI:6477402	M	MP:0011110	preweaning lethality, incomplete penetrance	Trp63<tm3.2Aam>/Trp63<+>	involves: 129S7/SvEvBrd * BALB/c * C57BL/6	N	23775923
MGI:6477412	M	MP:0006380	abnormal spermatid morphology	Cfap58<em1Fzh>/Cfap58<em1Fzh>	Not Specified	N	32791035
MGI:6477412	M	MP:0001925	male infertility	Cfap58<em1Fzh>/Cfap58<em1Fzh>	Not Specified	N	32791035
MGI:6477412	M	MP:0002687	oligozoospermia	Cfap58<em1Fzh>/Cfap58<em1Fzh>	Not Specified	N	32791035
MGI:6477412	M	MP:0002675	asthenozoospermia	Cfap58<em1Fzh>/Cfap58<em1Fzh>	Not Specified	N	32791035
MGI:6477412	M	MP:0020869	immotile sperm	Cfap58<em1Fzh>/Cfap58<em1Fzh>	Not Specified	N	32791035
MGI:6477412	M	MP:0009238	coiled sperm flagellum	Cfap58<em1Fzh>/Cfap58<em1Fzh>	Not Specified	N	32791035
MGI:6477412	M	MP:0009239	short sperm flagellum	Cfap58<em1Fzh>/Cfap58<em1Fzh>	Not Specified	N	32791035
MGI:6477412	M	MP:0005389	reproductive system phenotype	Cfap58<em1Fzh>/Cfap58<em1Fzh>	Not Specified	Y	32791035
MGI:6477558	M	MP:0005341	decreased susceptibility to atherosclerosis	Hhipl1<tm1a(KOMP)Wtsi>/Hhipl1<tm1a(KOMP)Wtsi>,Ldlr<tm1Her>/Ldlr<tm1Her>	involves: 129S7/SvEvBrd * C57BL/6J * C57BL/6N	N	31163988
MGI:6477559	M	MP:0005341	decreased susceptibility to atherosclerosis	Apoe<tm1Unc>/Apoe<tm1Unc>,Hhipl1<tm1a(KOMP)Wtsi>/Hhipl1<tm1a(KOMP)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J * C57BL/6N	N	31163988
MGI:6477565	M	MP:0004997	increased CNS synapse formation	Stau2<Gt(RRG396)Byg>/Stau2<Gt(RRG396)Byg>	B6.129P2-Stau2<Gt(RRG396)Byg>	N	30979012
MGI:6477565	M	MP:0002206	abnormal CNS synaptic transmission	Stau2<Gt(RRG396)Byg>/Stau2<Gt(RRG396)Byg>	B6.129P2-Stau2<Gt(RRG396)Byg>	N	30979012
MGI:6477565	M	MP:0002804	abnormal motor learning	Stau2<Gt(RRG396)Byg>/Stau2<Gt(RRG396)Byg>	B6.129P2-Stau2<Gt(RRG396)Byg>	N	30979012
MGI:6478181	F	MP:0002169	no abnormal phenotype detected	Bex2<tm1Kami>/Bex2<+>	C57BL/6NSlc-Bex2<tm1Kami>	N	25143383
MGI:6478183	M	MP:0002169	no abnormal phenotype detected	Bex2<tm1Kami>/Y	C57BL/6NSlc-Bex2<tm1Kami>	N	25143383
MGI:6478253	M	MP:0005389	reproductive system phenotype	4930447F04Rik<em1Utr>/Y	C57BL/6J-4930447F04Rik<em1Utr>	Y	32493902
MGI:6478255	M	MP:0005389	reproductive system phenotype	4933436I01Rik<em1Utr>/Y	C57BL/6J-4933436I01Rik<em1Utr>	N	32493902
MGI:6478257	M	MP:0005389	reproductive system phenotype	Ctag2<em1Utr>/Y	C57BL/6J-Ctag2<em1Utr>	N	32493902
MGI:6478259	M	MP:0005389	reproductive system phenotype	Del(XMir465d-Mir465)3Utr/Y	C57BL/6J-Del(XMir465d-Mir465)3Utr	N	32493902
MGI:6478261	M	MP:0005389	reproductive system phenotype	Gm1140<em1Utr>/Y	C57BL/6J-Gm1140<em1Utr>	N	32493902
MGI:6478263	M	MP:0005389	reproductive system phenotype	Gm14692<em1Utr>/Y	C57BL/6J-Gm14692<em1Utr>	N	32493902
MGI:6478265	M	MP:0005389	reproductive system phenotype	Gm6812<em1Utr>/Y	C57BL/6J-Gm6812<em1Utr>	N	32493902
MGI:6478268	M	MP:0005389	reproductive system phenotype	Mir743<em1Utr>/Y	C57BL/6J-Mir743<em1Utr>	N	32493902
MGI:6478826	M	MP:0002674	abnormal sperm motility	Efcab9<em1Chng>/Efcab9<em1Chng>	involves: C57BL/6	N	31056283
MGI:6478826	M	MP:0008892	abnormal sperm flagellum morphology	Efcab9<em1Chng>/Efcab9<em1Chng>	involves: C57BL/6	N	31056283
MGI:6478826	M	MP:0000242	impaired fertilization	Efcab9<em1Chng>/Efcab9<em1Chng>	involves: C57BL/6	N	31056283
MGI:6478826	M	MP:0004543	abnormal sperm physiology	Efcab9<em1Chng>/Efcab9<em1Chng>	involves: C57BL/6	N	31056283
MGI:6478826	M	MP:0001922	reduced male fertility	Efcab9<em1Chng>/Efcab9<em1Chng>	involves: C57BL/6	N	31056283
MGI:6478832	M	MP:0009282	decreased hyperactivated sperm motility	Catsperz<tm1(KOMP)Mbp>/Catsperz<tm1(KOMP)Mbp>,Efcab9<em1Chng>/Efcab9<em1Chng>	involves: C57BL/6 * C57BL/6N	N	31056283
MGI:6478832	M	MP:0001922	reduced male fertility	Catsperz<tm1(KOMP)Mbp>/Catsperz<tm1(KOMP)Mbp>,Efcab9<em1Chng>/Efcab9<em1Chng>	involves: C57BL/6 * C57BL/6N	N	31056283
MGI:6478834	M	MP:0001922	reduced male fertility	Efcab9<em2Chng>/Efcab9<em2Chng>	involves: C57BL/6	N	31056283
MGI:6479003	M	MP:0004542	impaired acrosome reaction	Iftap<tm1b(KOMP)Wtsi>/Iftap<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	30521625
MGI:6479003	M	MP:0009697	abnormal copulation behavior	Iftap<tm1b(KOMP)Wtsi>/Iftap<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	30521625
MGI:6479003	M	MP:0009230	abnormal sperm head morphology	Iftap<tm1b(KOMP)Wtsi>/Iftap<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	30521625
MGI:6479003	M	MP:0001922	reduced male fertility	Iftap<tm1b(KOMP)Wtsi>/Iftap<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	30521625
MGI:6479003	M	MP:0005389	reproductive system phenotype	Iftap<tm1b(KOMP)Wtsi>/Iftap<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	Y	30521625
MGI:6479003	M	MP:0000242	impaired fertilization	Iftap<tm1b(KOMP)Wtsi>/Iftap<tm1b(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	30521625
MGI:6479036	M	MP:0004852	decreased testis weight	Spata22<shani>/Spata22<shani>	C57BL/6J-Spata22<shani>	N	32388826
MGI:6479036	M	MP:0001925	male infertility	Spata22<shani>/Spata22<shani>	C57BL/6J-Spata22<shani>	N	32388826
MGI:6479036	M	MP:0014052	increased male germ cell apoptosis	Spata22<shani>/Spata22<shani>	C57BL/6J-Spata22<shani>	N	32388826
MGI:6479036	F	MP:0001127	small ovary	Spata22<shani>/Spata22<shani>	C57BL/6J-Spata22<shani>	N	32388826
MGI:6479036	M	MP:0010948	abnormal double-strand DNA break repair	Spata22<shani>/Spata22<shani>	C57BL/6J-Spata22<shani>	N	32388826
MGI:6479036	M	MP:0009451	abnormal chromosomal synapsis	Spata22<shani>/Spata22<shani>	C57BL/6J-Spata22<shani>	N	32388826
MGI:6479036	F	MP:0001926	female infertility	Spata22<shani>/Spata22<shani>	C57BL/6J-Spata22<shani>	N	32388826
MGI:6479036	M	MP:0001153	small seminiferous tubules	Spata22<shani>/Spata22<shani>	C57BL/6J-Spata22<shani>	N	32388826
MGI:6479036	F	MP:0002777	absent ovarian follicles	Spata22<shani>/Spata22<shani>	C57BL/6J-Spata22<shani>	N	32388826
MGI:6479036	M	MP:0008261	arrest of male meiosis	Spata22<shani>/Spata22<shani>	C57BL/6J-Spata22<shani>	N	32388826
MGI:6479076	M	MP:0005553	increased circulating creatinine level	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0005264	glomerulosclerosis	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0003215	renal interstitial fibrosis	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0002871	albuminuria	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0008140	podocyte foot process effacement	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0002083	premature death	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0011348	abnormal renal glomerulus basement membrane morphology	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0001262	decreased body weight	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0011353	expanded mesangial matrix	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0005567	decreased circulating total protein level	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0005161	hematuria	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0005565	increased blood urea nitrogen level	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0011409	increased renal glomerulus basement membrane thickness	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0002828	abnormal renal glomerular capsule morphology	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479076	M	MP:0005325	abnormal renal glomerulus morphology	Col4a5<em1Keha>/Y	C57BL/6J-Col4a5<em1Keha>	N	30582011
MGI:6479992	F	MP:0000220	increased monocyte cell number	Thop1<Gt(CSG163)Byg>/Thop1<Gt(CSG163)Byg>	B6.129P2-Thop1<Gt(CSG163)Byg>	N	31431000
MGI:6479992	F	MP:0005016	decreased lymphocyte cell number	Thop1<Gt(CSG163)Byg>/Thop1<Gt(CSG163)Byg>	B6.129P2-Thop1<Gt(CSG163)Byg>	N	31431000
MGI:6479992	F	MP:0000322	increased granulocyte number	Thop1<Gt(CSG163)Byg>/Thop1<Gt(CSG163)Byg>	B6.129P2-Thop1<Gt(CSG163)Byg>	N	31431000
MGI:6480012	M	MP:0005384	cellular phenotype	Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	Y	33082312
MGI:6480012	M	MP:0001524	impaired limb coordination	Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	33082312
MGI:6480012	M	MP:0005404	abnormal axon morphology	Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	33082312
MGI:6480012	M	MP:0020365	increased brain iron level	Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	33082312
MGI:6480012	M	MP:0011632	dilated mitochondrion	Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	33082312
MGI:6480012	M	MP:0001732	postnatal growth retardation	Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	33082312
MGI:6480012	M	MP:0000880	decreased Purkinje cell number	Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	33082312
MGI:6480012	M	MP:0001513	limb grasping	Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	33082312
MGI:6480012	M	MP:0002152	abnormal brain morphology	Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	33082312
MGI:6480012	M	MP:0001405	impaired coordination	Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	33082312
MGI:6480012	M	MP:0014185	cerebellum atrophy	Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	33082312
MGI:6480012	M	MP:0000876	Purkinje cell degeneration	Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	33082312
MGI:6480012	M	MP:0011743	abnormal Golgi apparatus morphology	Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * SJL	N	33082312
MGI:6480014	M	MP:0009378	abnormal endoplasmic reticulum morphology	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Nes-cre)1Kln/0	involves: C57BL/6NCrlj * CBA/JNCrlj * SJL	N	33082312
MGI:6480014	M	MP:0003631	nervous system phenotype	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Nes-cre)1Kln/0	involves: C57BL/6NCrlj * CBA/JNCrlj * SJL	Y	33082312
MGI:6480014	M	MP:0005384	cellular phenotype	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Nes-cre)1Kln/0	involves: C57BL/6NCrlj * CBA/JNCrlj * SJL	Y	33082312
MGI:6480015	M	MP:0000876	Purkinje cell degeneration	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * SJL	N	33082312
MGI:6480015	M	MP:0004098	abnormal cerebellar granule cell morphology	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * SJL	N	33082312
MGI:6480015	M	MP:0011743	abnormal Golgi apparatus morphology	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * SJL	N	33082312
MGI:6480015	M	MP:0005404	abnormal axon morphology	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * SJL	N	33082312
MGI:6480015	M	MP:0009378	abnormal endoplasmic reticulum morphology	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * SJL	N	33082312
MGI:6480015	M	MP:0011111	lethality during fetal growth through weaning, complete penetrance	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * SJL	N	33082312
MGI:6480015	M	MP:0011101	prenatal lethality, incomplete penetrance	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * SJL	N	33082312
MGI:6480015	M	MP:0001405	impaired coordination	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * SJL	N	33082312
MGI:6480015	M	MP:0014185	cerebellum atrophy	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * SJL	N	33082312
MGI:6480015	M	MP:0001732	postnatal growth retardation	Atg7<tm1Tchi>/Atg7<tm1Tchi>,Tg(Nes-cre)1Kln/0,Wdr45b<tm1c(EUCOMM)Hmgu>/Wdr45b<tm1c(EUCOMM)Hmgu>	involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * SJL	N	33082312
MGI:6480373	F	MP:0005655	increased aggression	4930579F01Rik<em1(IMPC)J>/4930579F01Rik<em1(IMPC)J>	C57BL/6NJ-4930579F01Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480373	F	MP:0001392	abnormal locomotor behavior	4930579F01Rik<em1(IMPC)J>/4930579F01Rik<em1(IMPC)J>	C57BL/6NJ-4930579F01Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480376	F	MP:0001415	increased exploration in new environment	Abca2<em1(IMPC)J>/Abca2<em1(IMPC)J>	C57BL/6NJ-Abca2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480376	F	MP:0010123	increased bone mineral content	Abca2<em1(IMPC)J>/Abca2<em1(IMPC)J>	C57BL/6NJ-Abca2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480376	F	MP:0010053	decreased grip strength	Abca2<em1(IMPC)J>/Abca2<em1(IMPC)J>	C57BL/6NJ-Abca2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480376	M	MP:0000367	abnormal coat/ hair morphology	Abca2<em1(IMPC)J>/Abca2<em1(IMPC)J>	C57BL/6NJ-Abca2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480376	F	MP:0001566	increased circulating phosphate level	Abca2<em1(IMPC)J>/Abca2<em1(IMPC)J>	C57BL/6NJ-Abca2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480377	M	MP:0002098	abnormal vibrissa morphology	Abca8a<em1(IMPC)J>/Abca8a<em1(IMPC)J>	C57BL/6NJ-Abca8a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480379	M	MP:0005627	increased circulating potassium level	Adam33<tm1b(EUCOMM)Hmgu>/Adam33<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adam33<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6480379	M	MP:0005553	increased circulating creatinine level	Adam33<tm1b(EUCOMM)Hmgu>/Adam33<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adam33<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6480381	F	MP:0001399	hyperactivity	Adck5<tm1.1(KOMP)Vlcg>/Adck5<tm1.1(KOMP)Vlcg>	B6N(Cg)-Adck5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6480381	F	MP:0002959	increased urine microalbumin level	Adck5<tm1.1(KOMP)Vlcg>/Adck5<tm1.1(KOMP)Vlcg>	B6N(Cg)-Adck5<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6480382	F	MP:0001293	anophthalmia	Aff4<em1(IMPC)Mbp>/Aff4<em1(IMPC)Mbp>	C57BL/6N-Aff4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480382	F	MP:0001711	abnormal placenta morphology	Aff4<em1(IMPC)Mbp>/Aff4<em1(IMPC)Mbp>	C57BL/6N-Aff4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480382	F	MP:0001785	edema	Aff4<em1(IMPC)Mbp>/Aff4<em1(IMPC)Mbp>	C57BL/6N-Aff4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480382	F	MP:0003231	abnormal placenta vasculature	Aff4<em1(IMPC)Mbp>/Aff4<em1(IMPC)Mbp>	C57BL/6N-Aff4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480382	F	MP:0000428	abnormal craniofacial morphology	Aff4<em1(IMPC)Mbp>/Aff4<em1(IMPC)Mbp>	C57BL/6N-Aff4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480383	F	MP:0002989	small kidney	Amtn<em1(IMPC)Mbp>/Amtn<em1(IMPC)Mbp>	C57BL/6N-Amtn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480383	M	MP:0000689	abnormal spleen morphology	Amtn<em1(IMPC)Mbp>/Amtn<em1(IMPC)Mbp>	C57BL/6N-Amtn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480383	F	MP:0000692	small spleen	Amtn<em1(IMPC)Mbp>/Amtn<em1(IMPC)Mbp>	C57BL/6N-Amtn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480384	F	MP:0000692	small spleen	Arhgap28<em1(IMPC)Mbp>/Arhgap28<em1(IMPC)Mbp>	C57BL/6NCrl-Arhgap28<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480384	F	MP:0009084	blind uterus	Arhgap28<em1(IMPC)Mbp>/Arhgap28<em1(IMPC)Mbp>	C57BL/6NCrl-Arhgap28<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480384	F	MP:0004258	abnormal placenta size	Arhgap28<em1(IMPC)Mbp>/Arhgap28<em1(IMPC)Mbp>	C57BL/6NCrl-Arhgap28<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480389	M	MP:0004958	enlarged prostate gland	Atl3<em1(IMPC)Tcp>/Atl3<em1(IMPC)Tcp>	C57BL/6N-Atl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480389	M	MP:0000702	enlarged lymph nodes	Atl3<em1(IMPC)Tcp>/Atl3<em1(IMPC)Tcp>	C57BL/6N-Atl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480389	F	MP:0002768	small adrenal glands	Atl3<em1(IMPC)Tcp>/Atl3<em1(IMPC)Tcp>	C57BL/6N-Atl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480389	M	MP:0011874	enlarged urinary bladder	Atl3<em1(IMPC)Tcp>/Atl3<em1(IMPC)Tcp>	C57BL/6N-Atl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480389	F	MP:0002989	small kidney	Atl3<em1(IMPC)Tcp>/Atl3<em1(IMPC)Tcp>	C57BL/6N-Atl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480389	F	MP:0000598	abnormal liver morphology	Atl3<em1(IMPC)Tcp>/Atl3<em1(IMPC)Tcp>	C57BL/6N-Atl3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480392	M	MP:0011962	increased cornea thickness	Bace2<tm1b(EUCOMM)Wtsi>/Bace2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Bace2<tm1b(EUCOMM)Wtsi>/Orl	N	MGI:5576271
MGI:6480393	M	MP:0004357	long tibia	Baiap2l1<em1(IMPC)Bay>/Baiap2l1<em1(IMPC)Bay>	C57BL/6N-Baiap2l1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480399	M	MP:0013279	increased fasting circulating glucose level	Bola1<tm1.1(KOMP)Vlcg>/Bola1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Bola1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6480399	F	MP:0010124	decreased bone mineral content	Bola1<tm1.1(KOMP)Vlcg>/Bola1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Bola1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6480399	F	MP:0002574	increased vertical activity	Bola1<tm1.1(KOMP)Vlcg>/Bola1<tm1.1(KOMP)Vlcg>	B6N(Cg)-Bola1<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6480404	M	MP:0002217	small lymph nodes	Calu<em1(IMPC)Tcp>/Calu<+>	C57BL/6N-Calu<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480405	M	MP:0001554	increased circulating free fatty acids level	Ccdc120<tm1.1(KOMP)Vlcg>/Y	B6N(Cg)-Ccdc120<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6480405	M	MP:0005560	decreased circulating glucose level	Ccdc120<tm1.1(KOMP)Vlcg>/Y	B6N(Cg)-Ccdc120<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6480406	F	MP:0003731	abnormal retina outer nuclear layer morphology	Ccdc181<tm1b(EUCOMM)Hmgu>/Ccdc181<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ccdc181<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6480409	F	MP:0000598	abnormal liver morphology	Ccn3<em1(IMPC)Mbp>/Ccn3<em1(IMPC)Mbp>	C57BL/6N-Ccn3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480409	F	MP:0001293	anophthalmia	Ccn3<em1(IMPC)Mbp>/Ccn3<em1(IMPC)Mbp>	C57BL/6N-Ccn3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480409	F	MP:0002699	abnormal vitreous body morphology	Ccn3<em1(IMPC)Mbp>/Ccn3<em1(IMPC)Mbp>	C57BL/6N-Ccn3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480409	F	MP:0009084	blind uterus	Ccn3<em1(IMPC)Mbp>/Ccn3<em1(IMPC)Mbp>	C57BL/6N-Ccn3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480409	M	MP:0002135	abnormal kidney morphology	Ccn3<em1(IMPC)Mbp>/Ccn3<em1(IMPC)Mbp>	C57BL/6N-Ccn3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480409	F	MP:0000689	abnormal spleen morphology	Ccn3<em1(IMPC)Mbp>/Ccn3<em1(IMPC)Mbp>	C57BL/6N-Ccn3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480409	F	MP:0000691	enlarged spleen	Ccn3<em1(IMPC)Mbp>/Ccn3<em1(IMPC)Mbp>	C57BL/6N-Ccn3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480409	M	MP:0003068	enlarged kidney	Ccn3<em1(IMPC)Mbp>/Ccn3<em1(IMPC)Mbp>	C57BL/6N-Ccn3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480410	F	MP:0001417	decreased exploration in new environment	Ccnj<em1(IMPC)J>/Ccnj<em1(IMPC)J>	C57BL/6NJ-Ccnj<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480411	M	MP:0010392	prolonged QRS complex duration	Pierce2<em1(IMPC)H>/Pierce2<em1(IMPC)H>	C57BL/6N-Pierce2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6480411	M	MP:0003900	shortened QT interval	Pierce2<em1(IMPC)H>/Pierce2<em1(IMPC)H>	C57BL/6N-Pierce2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6480412	M	MP:0009142	decreased prepulse inhibition	Ccsap<em1(IMPC)J>/Ccsap<em1(IMPC)J>	C57BL/6NJ-Ccsap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480413	F	MP:0002135	abnormal kidney morphology	Cd200r4<tm1.1(KOMP)Wtsi>/Cd200r4<tm1.1(KOMP)Wtsi>	C57BL/6N-Cd200r4<tm1.1(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6480414	F	MP:0002965	increased circulating serum albumin level	Cd209e<tm1b(KOMP)Wtsi>/Cd209e<tm1b(KOMP)Wtsi>	C57BL/6N-Cd209e<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6480415	M	MP:0010053	decreased grip strength	Cd2ap<em1(IMPC)Bay>/Cd2ap<em1(IMPC)Bay>	C57BL/6N-Cd2ap<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480416	M	MP:0002968	increased circulating alkaline phosphatase level	Cdh11<em1(IMPC)Mbp>/Cdh11<em1(IMPC)Mbp>	C57BL/6N-Cdh11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480416	F	MP:0002060	abnormal skin morphology	Cdh11<em1(IMPC)Mbp>/Cdh11<em1(IMPC)Mbp>	C57BL/6N-Cdh11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480416	M	MP:0000689	abnormal spleen morphology	Cdh11<em1(IMPC)Mbp>/Cdh11<em1(IMPC)Mbp>	C57BL/6N-Cdh11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480416	M	MP:0001147	small testis	Cdh11<em1(IMPC)Mbp>/Cdh11<em1(IMPC)Mbp>	C57BL/6N-Cdh11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480416	M	MP:0003068	enlarged kidney	Cdh11<em1(IMPC)Mbp>/Cdh11<em1(IMPC)Mbp>	C57BL/6N-Cdh11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480416	M	MP:0001146	abnormal testis morphology	Cdh11<em1(IMPC)Mbp>/Cdh11<em1(IMPC)Mbp>	C57BL/6N-Cdh11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480416	M	MP:0011496	abnormal head size	Cdh11<em1(IMPC)Mbp>/Cdh11<em1(IMPC)Mbp>	C57BL/6N-Cdh11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480416	M	MP:0000691	enlarged spleen	Cdh11<em1(IMPC)Mbp>/Cdh11<em1(IMPC)Mbp>	C57BL/6N-Cdh11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480416	M	MP:0000443	abnormal snout morphology	Cdh11<em1(IMPC)Mbp>/Cdh11<em1(IMPC)Mbp>	C57BL/6N-Cdh11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480422	M	MP:0010024	increased total body fat amount	Cebpz<tm1b(EUCOMM)Hmgu>/Cebpz<+>	C57BL/6N-Cebpz<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6480427	M	MP:0005419	decreased circulating serum albumin level	Cnbp<tm1b(KOMP)Wtsi>/Cnbp<+>	B6N(Cg)-Cnbp<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6480427	M	MP:0005566	decreased blood urea nitrogen level	Cnbp<tm1b(KOMP)Wtsi>/Cnbp<+>	B6N(Cg)-Cnbp<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6480428	F	MP:0001415	increased exploration in new environment	Cnksr2<em1(IMPC)J>/Cnksr2<em1(IMPC)J>	C57BL/6NJ-Cnksr2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6480428	F	MP:0003795	abnormal bone structure	Cnksr2<em1(IMPC)J>/Cnksr2<em1(IMPC)J>	C57BL/6NJ-Cnksr2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6480429	M	MP:0001402	decreased locomotor activity	Cnp<tm1b(EUCOMM)Wtsi>/Cnp<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cnp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6480429	M	MP:0020870	decreased thigmotaxis	Cnp<tm1b(EUCOMM)Wtsi>/Cnp<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cnp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6480429	M	MP:0004924	abnormal behavior	Cnp<tm1b(EUCOMM)Wtsi>/Cnp<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cnp<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6480431	M	MP:0020421	increased freezing behavior	Col17a1<em1(IMPC)Mbp>/Col17a1<em1(IMPC)Mbp>	C57BL/6N-Col17a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480431	F	MP:0005419	decreased circulating serum albumin level	Col17a1<em1(IMPC)Mbp>/Col17a1<em1(IMPC)Mbp>	C57BL/6N-Col17a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480431	F	MP:0009709	hydrometra	Col17a1<em1(IMPC)Mbp>/Col17a1<em1(IMPC)Mbp>	C57BL/6N-Col17a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480431	F	MP:0000195	decreased circulating calcium level	Col17a1<em1(IMPC)Mbp>/Col17a1<em1(IMPC)Mbp>	C57BL/6N-Col17a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480431	F	MP:0002060	abnormal skin morphology	Col17a1<em1(IMPC)Mbp>/Col17a1<em1(IMPC)Mbp>	C57BL/6N-Col17a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480433	M	MP:0003720	abnormal neural tube closure	Cox18<em1(IMPC)J>/Cox18<em1(IMPC)J>	C57BL/6NJ-Cox18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480438	M	MP:0002875	decreased erythrocyte cell number	Deup1<tm1.1(KOMP)Vlcg>/Deup1<tm1.1(KOMP)Vlcg>	C57BL/6N-Deup1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480438	M	MP:0002874	decreased hemoglobin content	Deup1<tm1.1(KOMP)Vlcg>/Deup1<tm1.1(KOMP)Vlcg>	C57BL/6N-Deup1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480438	F	MP:0000195	decreased circulating calcium level	Deup1<tm1.1(KOMP)Vlcg>/Deup1<tm1.1(KOMP)Vlcg>	C57BL/6N-Deup1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480438	M	MP:0000208	decreased hematocrit	Deup1<tm1.1(KOMP)Vlcg>/Deup1<tm1.1(KOMP)Vlcg>	C57BL/6N-Deup1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480440	F	MP:0003795	abnormal bone structure	Dipk2b<em1(IMPC)Mbp>/Dipk2b<em1(IMPC)Mbp>	C57BL/6N-Dipk2b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480440	F	MP:0020421	increased freezing behavior	Dipk2b<em1(IMPC)Mbp>/Dipk2b<em1(IMPC)Mbp>	C57BL/6N-Dipk2b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480440	F	MP:0009709	hydrometra	Dipk2b<em1(IMPC)Mbp>/Dipk2b<em1(IMPC)Mbp>	C57BL/6N-Dipk2b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480440	F	MP:0002060	abnormal skin morphology	Dipk2b<em1(IMPC)Mbp>/Dipk2b<em1(IMPC)Mbp>	C57BL/6N-Dipk2b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480440	F	MP:0000702	enlarged lymph nodes	Dipk2b<em1(IMPC)Mbp>/Dipk2b<em1(IMPC)Mbp>	C57BL/6N-Dipk2b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480440	F	MP:0001402	decreased locomotor activity	Dipk2b<em1(IMPC)Mbp>/Dipk2b<em1(IMPC)Mbp>	C57BL/6N-Dipk2b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480440	F	MP:0002339	abnormal lymph node morphology	Dipk2b<em1(IMPC)Mbp>/Dipk2b<em1(IMPC)Mbp>	C57BL/6N-Dipk2b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480444	F	MP:0005567	decreased circulating total protein level	Efcab7<em1(IMPC)J>/Efcab7<em1(IMPC)J>	C57BL/6NJ-Efcab7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480446	F	MP:0001700	abnormal embryo turning	Eloa<em1(IMPC)Mbp>/Eloa<em1(IMPC)Mbp>	C57BL/6N-Eloa<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480447	F	MP:0001417	decreased exploration in new environment	Elovl6<tm1b(EUCOMM)Hmgu>/Elovl6<+>	C57BL/6N-Elovl6<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6480447	M	MP:0010067	increased red blood cell distribution width	Elovl6<tm1b(EUCOMM)Hmgu>/Elovl6<+>	C57BL/6N-Elovl6<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6480448	F	MP:0002968	increased circulating alkaline phosphatase level	Enkur<em1(IMPC)Mbp>/Enkur<+>	C57BL/6N-Enkur<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6480448	M	MP:0002060	abnormal skin morphology	Enkur<em1(IMPC)Mbp>/Enkur<+>	C57BL/6N-Enkur<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6480449	M	MP:0000538	abnormal urinary bladder morphology	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	M	MP:0001146	abnormal testis morphology	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	M	MP:0011874	enlarged urinary bladder	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	M	MP:0003179	thrombocytopenia	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	M	MP:0000274	enlarged heart	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	M	MP:0005568	increased circulating total protein level	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	M	MP:0005178	increased circulating cholesterol level	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	M	MP:0000266	abnormal heart morphology	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	M	MP:0001147	small testis	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	M	MP:0002059	abnormal seminal vesicle morphology	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	M	MP:0002060	abnormal skin morphology	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	M	MP:0001556	increased circulating HDL cholesterol level	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	M	MP:0000598	abnormal liver morphology	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	F	MP:0004832	enlarged ovary	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	M	MP:0001157	small seminal vesicle	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480449	F	MP:0001126	abnormal ovary morphology	Entr1<em1(IMPC)Mbp>/Entr1<em1(IMPC)Mbp>	C57BL/6N-Entr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480452	M	MP:0000157	abnormal sternum morphology	Fbrsl1<em1(IMPC)Tcp>/Fbrsl1<em1(IMPC)Tcp>	C57BL/6N-Fbrsl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480452	M	MP:0000706	small thymus	Fbrsl1<em1(IMPC)Tcp>/Fbrsl1<em1(IMPC)Tcp>	C57BL/6N-Fbrsl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480452	M	MP:0001157	small seminal vesicle	Fbrsl1<em1(IMPC)Tcp>/Fbrsl1<em1(IMPC)Tcp>	C57BL/6N-Fbrsl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480452	M	MP:0004609	vertebral fusion	Fbrsl1<em1(IMPC)Tcp>/Fbrsl1<em1(IMPC)Tcp>	C57BL/6N-Fbrsl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480452	F	MP:0010067	increased red blood cell distribution width	Fbrsl1<em1(IMPC)Tcp>/Fbrsl1<em1(IMPC)Tcp>	C57BL/6N-Fbrsl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480452	M	MP:0010392	prolonged QRS complex duration	Fbrsl1<em1(IMPC)Tcp>/Fbrsl1<em1(IMPC)Tcp>	C57BL/6N-Fbrsl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480452	M	MP:0000691	enlarged spleen	Fbrsl1<em1(IMPC)Tcp>/Fbrsl1<em1(IMPC)Tcp>	C57BL/6N-Fbrsl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480452	M	MP:0001325	abnormal retina morphology	Fbrsl1<em1(IMPC)Tcp>/Fbrsl1<em1(IMPC)Tcp>	C57BL/6N-Fbrsl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480452	M	MP:0004930	small epididymis	Fbrsl1<em1(IMPC)Tcp>/Fbrsl1<em1(IMPC)Tcp>	C57BL/6N-Fbrsl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480452	M	MP:0002111	abnormal tail morphology	Fbrsl1<em1(IMPC)Tcp>/Fbrsl1<em1(IMPC)Tcp>	C57BL/6N-Fbrsl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480452	F	MP:0000598	abnormal liver morphology	Fbrsl1<em1(IMPC)Tcp>/Fbrsl1<em1(IMPC)Tcp>	C57BL/6N-Fbrsl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480452	M	MP:0001147	small testis	Fbrsl1<em1(IMPC)Tcp>/Fbrsl1<em1(IMPC)Tcp>	C57BL/6N-Fbrsl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480454	F	MP:0002953	thick ventricular wall	Fcrl6<tm1b(KOMP)Wtsi>/Fcrl6<tm1b(KOMP)Wtsi>	C57BL/6N-Fcrl6<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6480457	M	MP:0001415	increased exploration in new environment	Focad<em1(IMPC)Bay>/Focad<+>	C57BL/6N-Focad<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480458	F	MP:0004122	abnormal sinus arrhythmia	Foxj3<tm1a(EUCOMM)Wtsi>/Foxj3<+>	C57BL/6N-Foxj3<tm1a(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6480465	F	MP:0001486	abnormal startle reflex	Iigp1c<em1(IMPC)Hmgu>/Iigp1c<em1(IMPC)Hmgu>	C57BL/6N-Iigp1c<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6480465	M	MP:0002833	increased heart weight	Iigp1c<em1(IMPC)Hmgu>/Iigp1c<em1(IMPC)Hmgu>	C57BL/6N-Iigp1c<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6480465	M	MP:0010052	increased grip strength	Iigp1c<em1(IMPC)Hmgu>/Iigp1c<em1(IMPC)Hmgu>	C57BL/6N-Iigp1c<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6480465	M	MP:0002135	abnormal kidney morphology	Iigp1c<em1(IMPC)Hmgu>/Iigp1c<em1(IMPC)Hmgu>	C57BL/6N-Iigp1c<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6480465	F	MP:0002590	increased mean corpuscular volume	Iigp1c<em1(IMPC)Hmgu>/Iigp1c<em1(IMPC)Hmgu>	C57BL/6N-Iigp1c<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6480465	M	MP:0001406	abnormal gait	Iigp1c<em1(IMPC)Hmgu>/Iigp1c<em1(IMPC)Hmgu>	C57BL/6N-Iigp1c<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6480465	F	MP:0002339	abnormal lymph node morphology	Iigp1c<em1(IMPC)Hmgu>/Iigp1c<em1(IMPC)Hmgu>	C57BL/6N-Iigp1c<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6480468	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Gpc4<tm2b(EUCOMM)Wtsi>/Y	C57BL/6N-Gpc4<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6480468	M	MP:0005554	decreased circulating creatinine level	Gpc4<tm2b(EUCOMM)Wtsi>/Y	C57BL/6N-Gpc4<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6480468	M	MP:0001314	cornea opacity	Gpc4<tm2b(EUCOMM)Wtsi>/Y	C57BL/6N-Gpc4<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6480468	M	MP:0013278	decreased fasting circulating glucose level	Gpc4<tm2b(EUCOMM)Wtsi>/Y	C57BL/6N-Gpc4<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6480468	M	MP:0005566	decreased blood urea nitrogen level	Gpc4<tm2b(EUCOMM)Wtsi>/Y	C57BL/6N-Gpc4<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6480468	M	MP:0005561	increased mean corpuscular hemoglobin	Gpc4<tm2b(EUCOMM)Wtsi>/Y	C57BL/6N-Gpc4<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6480468	M	MP:0005344	increased circulating bilirubin level	Gpc4<tm2b(EUCOMM)Wtsi>/Y	C57BL/6N-Gpc4<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6480475	M	MP:0002606	increased basophil cell number	Has1<tm1b(KOMP)Wtsi>/Has1<tm1b(KOMP)Wtsi>	C57BL/6N-Has1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6480475	M	MP:0005012	decreased eosinophil cell number	Has1<tm1b(KOMP)Wtsi>/Has1<tm1b(KOMP)Wtsi>	C57BL/6N-Has1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6480477	F	MP:0003795	abnormal bone structure	Htr3b<tm1.1(KOMP)Vlcg>/Htr3b<tm1.1(KOMP)Vlcg>	C57BL/6N-Htr3b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6480478	M	MP:0003960	increased lean body mass	Ifitm1<tm1b(EUCOMM)Wtsi>/Ifitm1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Ifitm1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6480482	F	MP:0005178	increased circulating cholesterol level	Ing5<em1(IMPC)J>/Ing5<em1(IMPC)J>	C57BL/6NJ-Ing5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480482	M	MP:0000443	abnormal snout morphology	Ing5<em1(IMPC)J>/Ing5<em1(IMPC)J>	C57BL/6NJ-Ing5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480482	F	MP:0005542	cornea vascularization	Ing5<em1(IMPC)J>/Ing5<em1(IMPC)J>	C57BL/6NJ-Ing5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480482	F	MP:0012121	sclerocornea	Ing5<em1(IMPC)J>/Ing5<em1(IMPC)J>	C57BL/6NJ-Ing5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480482	F	MP:0013279	increased fasting circulating glucose level	Ing5<em1(IMPC)J>/Ing5<em1(IMPC)J>	C57BL/6NJ-Ing5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480482	F	MP:0010392	prolonged QRS complex duration	Ing5<em1(IMPC)J>/Ing5<em1(IMPC)J>	C57BL/6NJ-Ing5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480484	M	MP:0001691	abnormal somite shape	Isyna1<em1(IMPC)Bay>/Isyna1<em1(IMPC)Bay>	C57BL/6N-Isyna1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480484	M	MP:0002111	abnormal tail morphology	Isyna1<em1(IMPC)Bay>/Isyna1<em1(IMPC)Bay>	C57BL/6N-Isyna1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480484	M	MP:0002109	abnormal limb morphology	Isyna1<em1(IMPC)Bay>/Isyna1<em1(IMPC)Bay>	C57BL/6N-Isyna1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480484	M	MP:0000564	syndactyly	Isyna1<em1(IMPC)Bay>/Isyna1<em1(IMPC)Bay>	C57BL/6N-Isyna1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480484	M	MP:0001722	pale yolk sac	Isyna1<em1(IMPC)Bay>/Isyna1<em1(IMPC)Bay>	C57BL/6N-Isyna1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480484	M	MP:0003720	abnormal neural tube closure	Isyna1<em1(IMPC)Bay>/Isyna1<em1(IMPC)Bay>	C57BL/6N-Isyna1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480484	M	MP:0000269	abnormal heart looping	Isyna1<em1(IMPC)Bay>/Isyna1<em1(IMPC)Bay>	C57BL/6N-Isyna1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480485	F	MP:0002339	abnormal lymph node morphology	Jak3<em1(IMPC)Mbp>/Jak3<+>	C57BL/6N-Jak3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480485	F	MP:0000689	abnormal spleen morphology	Jak3<em1(IMPC)Mbp>/Jak3<+>	C57BL/6N-Jak3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480485	F	MP:0020870	decreased thigmotaxis	Jak3<em1(IMPC)Mbp>/Jak3<+>	C57BL/6N-Jak3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480485	F	MP:0000702	enlarged lymph nodes	Jak3<em1(IMPC)Mbp>/Jak3<+>	C57BL/6N-Jak3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480485	F	MP:0000691	enlarged spleen	Jak3<em1(IMPC)Mbp>/Jak3<+>	C57BL/6N-Jak3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480485	F	MP:0001364	decreased anxiety-related response	Jak3<em1(IMPC)Mbp>/Jak3<+>	C57BL/6N-Jak3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480485	F	MP:0001399	hyperactivity	Jak3<em1(IMPC)Mbp>/Jak3<+>	C57BL/6N-Jak3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480485	F	MP:0004924	abnormal behavior	Jak3<em1(IMPC)Mbp>/Jak3<+>	C57BL/6N-Jak3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480485	F	MP:0001417	decreased exploration in new environment	Jak3<em1(IMPC)Mbp>/Jak3<+>	C57BL/6N-Jak3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480487	F	MP:0011110	preweaning lethality, incomplete penetrance	Jcad<em1(IMPC)Bay>/Jcad<em1(IMPC)Bay>	C57BL/6N-Jcad<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480489	M	MP:0005630	increased lung weight	Kcnd1<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Kcnd1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480493	F	MP:0002092	abnormal eye morphology	Lmod3<em1(IMPC)Mbp>/Lmod3<+>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6480493	F	MP:0002135	abnormal kidney morphology	Lmod3<em1(IMPC)Mbp>/Lmod3<+>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6480493	M	MP:0005565	increased blood urea nitrogen level	Lmod3<em1(IMPC)Mbp>/Lmod3<+>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6480493	F	MP:0003131	increased erythrocyte cell number	Lmod3<em1(IMPC)Mbp>/Lmod3<+>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6480493	F	MP:0003068	enlarged kidney	Lmod3<em1(IMPC)Mbp>/Lmod3<+>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6480493	F	MP:0009084	blind uterus	Lmod3<em1(IMPC)Mbp>/Lmod3<+>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6480493	F	MP:0002608	increased hematocrit	Lmod3<em1(IMPC)Mbp>/Lmod3<+>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6480493	F	MP:0002188	small heart	Lmod3<em1(IMPC)Mbp>/Lmod3<+>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6480493	F	MP:0000266	abnormal heart morphology	Lmod3<em1(IMPC)Mbp>/Lmod3<+>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6480493	F	MP:0005564	increased hemoglobin content	Lmod3<em1(IMPC)Mbp>/Lmod3<+>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6480493	F	MP:0002989	small kidney	Lmod3<em1(IMPC)Mbp>/Lmod3<+>	C57BL/6N-Lmod3<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6480494	F	MP:0005333	decreased heart rate	Lmtk2<em1(IMPC)Mbp>/Lmtk2<em1(IMPC)Mbp>	C57BL/6N-Lmtk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480494	M	MP:0001146	abnormal testis morphology	Lmtk2<em1(IMPC)Mbp>/Lmtk2<em1(IMPC)Mbp>	C57BL/6N-Lmtk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480494	F	MP:0010506	prolonged RR interval	Lmtk2<em1(IMPC)Mbp>/Lmtk2<em1(IMPC)Mbp>	C57BL/6N-Lmtk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480494	M	MP:0001147	small testis	Lmtk2<em1(IMPC)Mbp>/Lmtk2<em1(IMPC)Mbp>	C57BL/6N-Lmtk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480494	F	MP:0000274	enlarged heart	Lmtk2<em1(IMPC)Mbp>/Lmtk2<em1(IMPC)Mbp>	C57BL/6N-Lmtk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480494	F	MP:0002989	small kidney	Lmtk2<em1(IMPC)Mbp>/Lmtk2<em1(IMPC)Mbp>	C57BL/6N-Lmtk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480494	F	MP:0000266	abnormal heart morphology	Lmtk2<em1(IMPC)Mbp>/Lmtk2<em1(IMPC)Mbp>	C57BL/6N-Lmtk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480494	F	MP:0002968	increased circulating alkaline phosphatase level	Lmtk2<em1(IMPC)Mbp>/Lmtk2<em1(IMPC)Mbp>	C57BL/6N-Lmtk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480494	F	MP:0002135	abnormal kidney morphology	Lmtk2<em1(IMPC)Mbp>/Lmtk2<em1(IMPC)Mbp>	C57BL/6N-Lmtk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480494	F	MP:0001258	decreased body length	Lmtk2<em1(IMPC)Mbp>/Lmtk2<em1(IMPC)Mbp>	C57BL/6N-Lmtk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480494	M	MP:0001925	male infertility	Lmtk2<em1(IMPC)Mbp>/Lmtk2<em1(IMPC)Mbp>	C57BL/6N-Lmtk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480496	M	MP:0011436	decreased urine magnesium level	Lpar4<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Lpar4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6480496	M	MP:0010053	decreased grip strength	Lpar4<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Lpar4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6480497	F	MP:0011436	decreased urine magnesium level	Lpar4<tm1.1(KOMP)Vlcg>/Lpar4<tm1.1(KOMP)Vlcg>	C57BL/6N-Lpar4<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6480500	F	MP:0002966	decreased circulating alkaline phosphatase level	Ltn1<tm1b(EUCOMM)Hmgu>/Ltn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ltn1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6480500	F	MP:0001262	decreased body weight	Ltn1<tm1b(EUCOMM)Hmgu>/Ltn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ltn1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6480500	F	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	Ltn1<tm1b(EUCOMM)Hmgu>/Ltn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ltn1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6480500	F	MP:0011047	increased lung tissue damping	Ltn1<tm1b(EUCOMM)Hmgu>/Ltn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ltn1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6480500	F	MP:0003179	thrombocytopenia	Ltn1<tm1b(EUCOMM)Hmgu>/Ltn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ltn1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6480500	F	MP:0010067	increased red blood cell distribution width	Ltn1<tm1b(EUCOMM)Hmgu>/Ltn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ltn1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6480500	F	MP:0011044	increased lung elastance	Ltn1<tm1b(EUCOMM)Hmgu>/Ltn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ltn1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6480500	F	MP:0001312	abnormal cornea morphology	Ltn1<tm1b(EUCOMM)Hmgu>/Ltn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ltn1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6480500	F	MP:0010935	increased airway resistance	Ltn1<tm1b(EUCOMM)Hmgu>/Ltn1<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ltn1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6480501	M	MP:0002059	abnormal seminal vesicle morphology	Magt1<em1(IMPC)Tcp>/Y	C57BL/6N-Magt1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480505	M	MP:0000219	increased neutrophil cell number	Mfsd1<em1(IMPC)Tcp>/Mfsd1<em1(IMPC)Tcp>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480505	M	MP:0005344	increased circulating bilirubin level	Mfsd1<em1(IMPC)Tcp>/Mfsd1<em1(IMPC)Tcp>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480505	M	MP:0002968	increased circulating alkaline phosphatase level	Mfsd1<em1(IMPC)Tcp>/Mfsd1<em1(IMPC)Tcp>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480505	M	MP:0003179	thrombocytopenia	Mfsd1<em1(IMPC)Tcp>/Mfsd1<em1(IMPC)Tcp>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480505	F	MP:0000157	abnormal sternum morphology	Mfsd1<em1(IMPC)Tcp>/Mfsd1<em1(IMPC)Tcp>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480505	M	MP:0010067	increased red blood cell distribution width	Mfsd1<em1(IMPC)Tcp>/Mfsd1<em1(IMPC)Tcp>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480505	M	MP:0000221	decreased leukocyte cell number	Mfsd1<em1(IMPC)Tcp>/Mfsd1<em1(IMPC)Tcp>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480505	M	MP:0001289	persistence of hyaloid vascular system	Mfsd1<em1(IMPC)Tcp>/Mfsd1<em1(IMPC)Tcp>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480505	M	MP:0002644	decreased circulating triglyceride level	Mfsd1<em1(IMPC)Tcp>/Mfsd1<em1(IMPC)Tcp>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480505	M	MP:0001147	small testis	Mfsd1<em1(IMPC)Tcp>/Mfsd1<em1(IMPC)Tcp>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480505	M	MP:0002599	increased mean platelet volume	Mfsd1<em1(IMPC)Tcp>/Mfsd1<em1(IMPC)Tcp>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480505	M	MP:0005016	decreased lymphocyte cell number	Mfsd1<em1(IMPC)Tcp>/Mfsd1<em1(IMPC)Tcp>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480505	M	MP:0005343	increased circulating aspartate transaminase level	Mfsd1<em1(IMPC)Tcp>/Mfsd1<em1(IMPC)Tcp>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480507	F	MP:0002075	abnormal coat/hair pigmentation	Mical3<em1(IMPC)J>/Mical3<em1(IMPC)J>	C57BL/6NJ-Mical3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480507	F	MP:0001529	abnormal vocalization	Mical3<em1(IMPC)J>/Mical3<em1(IMPC)J>	C57BL/6NJ-Mical3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480507	F	MP:0001399	hyperactivity	Mical3<em1(IMPC)J>/Mical3<em1(IMPC)J>	C57BL/6NJ-Mical3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480509	F	MP:0008797	facial cleft	Mllt10<em1(IMPC)Mbp>/Mllt10<em1(IMPC)Mbp>	C57BL/6N-Mllt10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480510	M	MP:0001297	microphthalmia	Morc4<em1(IMPC)Mbp>/Y	C57BL/6N-Morc4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480510	M	MP:0003900	shortened QT interval	Morc4<em1(IMPC)Mbp>/Y	C57BL/6N-Morc4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480510	M	MP:0000702	enlarged lymph nodes	Morc4<em1(IMPC)Mbp>/Y	C57BL/6N-Morc4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480510	M	MP:0002339	abnormal lymph node morphology	Morc4<em1(IMPC)Mbp>/Y	C57BL/6N-Morc4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480510	M	MP:0002092	abnormal eye morphology	Morc4<em1(IMPC)Mbp>/Y	C57BL/6N-Morc4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480511	F	MP:0005553	increased circulating creatinine level	Morc4<em1(IMPC)Mbp>/Morc4<em1(IMPC)Mbp>	C57BL/6N-Morc4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480511	F	MP:0002339	abnormal lymph node morphology	Morc4<em1(IMPC)Mbp>/Morc4<em1(IMPC)Mbp>	C57BL/6N-Morc4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480511	F	MP:0000702	enlarged lymph nodes	Morc4<em1(IMPC)Mbp>/Morc4<em1(IMPC)Mbp>	C57BL/6N-Morc4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480512	F	MP:0001891	hydrocephaly	Mpv17l2<tm1.1(KOMP)Mbp>/Mpv17l2<+>	C57BL/6N-Mpv17l2<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6480514	F	MP:0003179	thrombocytopenia	Msn<tm1b(EUCOMM)Hmgu>/Msn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Msn<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480514	F	MP:0000208	decreased hematocrit	Msn<tm1b(EUCOMM)Hmgu>/Msn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Msn<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480514	F	MP:0002833	increased heart weight	Msn<tm1b(EUCOMM)Hmgu>/Msn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Msn<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480514	F	MP:0002874	decreased hemoglobin content	Msn<tm1b(EUCOMM)Hmgu>/Msn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Msn<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480514	F	MP:0000221	decreased leukocyte cell number	Msn<tm1b(EUCOMM)Hmgu>/Msn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Msn<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480514	F	MP:0002590	increased mean corpuscular volume	Msn<tm1b(EUCOMM)Hmgu>/Msn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Msn<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480514	F	MP:0005561	increased mean corpuscular hemoglobin	Msn<tm1b(EUCOMM)Hmgu>/Msn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Msn<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480514	F	MP:0002875	decreased erythrocyte cell number	Msn<tm1b(EUCOMM)Hmgu>/Msn<tm1b(EUCOMM)Hmgu>	C57BL/6N-Msn<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480515	F	MP:0000601	small liver	Mtap<em1(IMPC)Mbp>/Mtap<+>	C57BL/6N-Mtap<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480515	F	MP:0000703	abnormal thymus morphology	Mtap<em1(IMPC)Mbp>/Mtap<+>	C57BL/6N-Mtap<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480515	F	MP:0000274	enlarged heart	Mtap<em1(IMPC)Mbp>/Mtap<+>	C57BL/6N-Mtap<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480515	F	MP:0000702	enlarged lymph nodes	Mtap<em1(IMPC)Mbp>/Mtap<+>	C57BL/6N-Mtap<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480515	F	MP:0000266	abnormal heart morphology	Mtap<em1(IMPC)Mbp>/Mtap<+>	C57BL/6N-Mtap<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480515	F	MP:0000709	enlarged thymus	Mtap<em1(IMPC)Mbp>/Mtap<+>	C57BL/6N-Mtap<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480515	F	MP:0002339	abnormal lymph node morphology	Mtap<em1(IMPC)Mbp>/Mtap<+>	C57BL/6N-Mtap<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480516	M	MP:0010067	increased red blood cell distribution width	Mtmr1<tm2b(KOMP)Wtsi>/Y	C57BL/6N-Mtmr1<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6480516	M	MP:0002599	increased mean platelet volume	Mtmr1<tm2b(KOMP)Wtsi>/Y	C57BL/6N-Mtmr1<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6480517	F	MP:0010024	increased total body fat amount	Mtmr1<tm2b(KOMP)Wtsi>/Mtmr1<tm2b(KOMP)Wtsi>	C57BL/6N-Mtmr1<tm2b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6480522	M	MP:0002753	dilated heart left ventricle	Ncam2<tm1b(EUCOMM)Hmgu>/Ncam2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ncam2<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6480522	M	MP:0005011	increased eosinophil cell number	Ncam2<tm1b(EUCOMM)Hmgu>/Ncam2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ncam2<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6480522	M	MP:0001417	decreased exploration in new environment	Ncam2<tm1b(EUCOMM)Hmgu>/Ncam2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Ncam2<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6480526	F	MP:0001325	abnormal retina morphology	Nlrx1<em1(IMPC)Mbp>/Nlrx1<em1(IMPC)Mbp>	C57BL/6N-Nlrx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480526	F	MP:0009084	blind uterus	Nlrx1<em1(IMPC)Mbp>/Nlrx1<em1(IMPC)Mbp>	C57BL/6N-Nlrx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480526	M	MP:0000692	small spleen	Nlrx1<em1(IMPC)Mbp>/Nlrx1<em1(IMPC)Mbp>	C57BL/6N-Nlrx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480527	F	MP:0009709	hydrometra	Nnmt<em1(IMPC)Mbp>/Nnmt<em1(IMPC)Mbp>	C57BL/6NCrl-Nnmt<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480527	M	MP:0000689	abnormal spleen morphology	Nnmt<em1(IMPC)Mbp>/Nnmt<em1(IMPC)Mbp>	C57BL/6NCrl-Nnmt<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480527	M	MP:0000691	enlarged spleen	Nnmt<em1(IMPC)Mbp>/Nnmt<em1(IMPC)Mbp>	C57BL/6NCrl-Nnmt<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480527	F	MP:0001120	abnormal uterus morphology	Nnmt<em1(IMPC)Mbp>/Nnmt<em1(IMPC)Mbp>	C57BL/6NCrl-Nnmt<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480527	F	MP:0001944	abnormal pancreas morphology	Nnmt<em1(IMPC)Mbp>/Nnmt<em1(IMPC)Mbp>	C57BL/6NCrl-Nnmt<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480527	F	MP:0001126	abnormal ovary morphology	Nnmt<em1(IMPC)Mbp>/Nnmt<em1(IMPC)Mbp>	C57BL/6NCrl-Nnmt<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480527	M	MP:0002060	abnormal skin morphology	Nnmt<em1(IMPC)Mbp>/Nnmt<em1(IMPC)Mbp>	C57BL/6NCrl-Nnmt<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480527	F	MP:0004832	enlarged ovary	Nnmt<em1(IMPC)Mbp>/Nnmt<em1(IMPC)Mbp>	C57BL/6NCrl-Nnmt<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480532	M	MP:0009142	decreased prepulse inhibition	Nrp1<tm1b(EUCOMM)Hmgu>/Nrp1<+>	C57BL/6N-Nrp1<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6480535	M	MP:0010087	increased circulating fructosamine level	Nubp2<tm1b(EUCOMM)Hmgu>/Nubp2<+>	C57BL/6N-Nubp2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6480535	F	MP:0002764	short tibia	Nubp2<tm1b(EUCOMM)Hmgu>/Nubp2<+>	C57BL/6N-Nubp2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6480537	M	MP:0002965	increased circulating serum albumin level	Or9g4<em1(IMPC)Mbp>/Or9g4<em1(IMPC)Mbp>	C57BL/6N-Or9g4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480537	F	MP:0002188	small heart	Or9g4<em1(IMPC)Mbp>/Or9g4<em1(IMPC)Mbp>	C57BL/6N-Or9g4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480537	F	MP:0000266	abnormal heart morphology	Or9g4<em1(IMPC)Mbp>/Or9g4<em1(IMPC)Mbp>	C57BL/6N-Or9g4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480537	F	MP:0001944	abnormal pancreas morphology	Or9g4<em1(IMPC)Mbp>/Or9g4<em1(IMPC)Mbp>	C57BL/6N-Or9g4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480537	M	MP:0005178	increased circulating cholesterol level	Or9g4<em1(IMPC)Mbp>/Or9g4<em1(IMPC)Mbp>	C57BL/6N-Or9g4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480537	M	MP:0000598	abnormal liver morphology	Or9g4<em1(IMPC)Mbp>/Or9g4<em1(IMPC)Mbp>	C57BL/6N-Or9g4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480537	F	MP:0002339	abnormal lymph node morphology	Or9g4<em1(IMPC)Mbp>/Or9g4<em1(IMPC)Mbp>	C57BL/6N-Or9g4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480537	F	MP:0002060	abnormal skin morphology	Or9g4<em1(IMPC)Mbp>/Or9g4<em1(IMPC)Mbp>	C57BL/6N-Or9g4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480537	M	MP:0005568	increased circulating total protein level	Or9g4<em1(IMPC)Mbp>/Or9g4<em1(IMPC)Mbp>	C57BL/6N-Or9g4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480537	F	MP:0000702	enlarged lymph nodes	Or9g4<em1(IMPC)Mbp>/Or9g4<em1(IMPC)Mbp>	C57BL/6N-Or9g4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480537	M	MP:0001148	enlarged testis	Or9g4<em1(IMPC)Mbp>/Or9g4<em1(IMPC)Mbp>	C57BL/6N-Or9g4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480537	M	MP:0001146	abnormal testis morphology	Or9g4<em1(IMPC)Mbp>/Or9g4<em1(IMPC)Mbp>	C57BL/6N-Or9g4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480537	M	MP:0001556	increased circulating HDL cholesterol level	Or9g4<em1(IMPC)Mbp>/Or9g4<em1(IMPC)Mbp>	C57BL/6N-Or9g4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480539	F	MP:0002098	abnormal vibrissa morphology	Otog<em1(IMPC)J>/Otog<em1(IMPC)J>	C57BL/6NJ-Otog<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480541	M	MP:0001147	small testis	P2rx2<tm1b(EUCOMM)Hmgu>/P2rx2<tm1b(EUCOMM)Hmgu>	C57BL/6N-P2rx2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6480541	M	MP:0001417	decreased exploration in new environment	P2rx2<tm1b(EUCOMM)Hmgu>/P2rx2<tm1b(EUCOMM)Hmgu>	C57BL/6N-P2rx2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6480543	F	MP:0005293	impaired glucose tolerance	Pcdh8<em1(IMPC)H>/Pcdh8<em1(IMPC)H>	C57BL/6N-Pcdh8<em1(IMPC)H>/H	N	MGI:5576271
MGI:6480544	M	MP:0010124	decreased bone mineral content	Pcnx2<em1(IMPC)J>/Pcnx2<+>	C57BL/6NJ-Pcnx2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6480544	M	MP:0005568	increased circulating total protein level	Pcnx2<em1(IMPC)J>/Pcnx2<+>	C57BL/6NJ-Pcnx2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6480544	M	MP:0000063	decreased bone mineral density	Pcnx2<em1(IMPC)J>/Pcnx2<+>	C57BL/6NJ-Pcnx2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6480549	F	MP:0001120	abnormal uterus morphology	Phka1<em1(IMPC)Tcp>/Phka1<em1(IMPC)Tcp>	C57BL/6N-Phka1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480550	F	MP:0013278	decreased fasting circulating glucose level	Pigc<em1(IMPC)J>/Pigc<+>	C57BL/6NJ-Pigc<em1(IMPC)J>/J	N	MGI:5576271
MGI:6480550	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Pigc<em1(IMPC)J>/Pigc<+>	C57BL/6NJ-Pigc<em1(IMPC)J>/J	N	MGI:5576271
MGI:6480551	M	MP:0005561	increased mean corpuscular hemoglobin	Plxna2<tm1a(EUCOMM)Wtsi>/Plxna2<tm1a(EUCOMM)Wtsi>	C57BL/6N-Plxna2<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6480552	M	MP:0005574	decreased pulmonary respiratory rate	Pnck<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Pnck<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6480552	M	MP:0005586	decreased tidal volume	Pnck<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Pnck<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6480552	M	MP:0005576	decreased pulmonary ventilation	Pnck<tm1b(KOMP)Wtsi>/Y	C57BL/6N-Pnck<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6480553	F	MP:0005586	decreased tidal volume	Pnck<tm1b(KOMP)Wtsi>/Pnck<tm1b(KOMP)Wtsi>	C57BL/6N-Pnck<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6480556	F	MP:0011100	preweaning lethality, complete penetrance	Pou1f1<em1(IMPC)Bay>/Pou1f1<em1(IMPC)Bay>	C57BL/6N-Pou1f1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480557	F	MP:0011110	preweaning lethality, incomplete penetrance	Ppdpf<tm1.1(KOMP)Mbp>/Ppdpf<tm1.1(KOMP)Mbp>	C57BL/6N-Ppdpf<tm1.1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480562	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Rab11b<em1(IMPC)J>/Rab11b<em1(IMPC)J>	C57BL/6NJ-Rab11b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6480563	F	MP:0013279	increased fasting circulating glucose level	Rab11fip1<em1(IMPC)Bay>/Rab11fip1<em1(IMPC)Bay>	C57BL/6N-Rab11fip1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480566	F	MP:0001289	persistence of hyaloid vascular system	Rbbp8nl<em1(IMPC)J>/Rbbp8nl<em1(IMPC)J>	C57BL/6NJ-Rbbp8nl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480567	F	MP:0002079	increased circulating insulin level	Rbmx<tm2a(KOMP)Wtsi>/Rbmx<tm2a(KOMP)Wtsi>	C57BL/6N-Rbmx<tm2a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6480568	M	MP:0001258	decreased body length	Rbmx<tm2b(KOMP)Wtsi>/Y	C57BL/6N-Rbmx<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6480568	M	MP:0003917	increased kidney weight	Rbmx<tm2b(KOMP)Wtsi>/Y	C57BL/6N-Rbmx<tm2b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6480569	F	MP:0002968	increased circulating alkaline phosphatase level	Rbpms<em1(IMPC)H>/Rbpms<+>	C57BL/6NTac-Rbpms<em1(IMPC)H>/H	N	MGI:5576271
MGI:6480572	M	MP:0002599	increased mean platelet volume	Rit1<em1(IMPC)Mbp>/Rit1<em1(IMPC)Mbp>	C57BL/6N-Rit1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480572	F	MP:0002968	increased circulating alkaline phosphatase level	Rit1<em1(IMPC)Mbp>/Rit1<em1(IMPC)Mbp>	C57BL/6N-Rit1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480572	M	MP:0002135	abnormal kidney morphology	Rit1<em1(IMPC)Mbp>/Rit1<em1(IMPC)Mbp>	C57BL/6N-Rit1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480572	F	MP:0010067	increased red blood cell distribution width	Rit1<em1(IMPC)Mbp>/Rit1<em1(IMPC)Mbp>	C57BL/6N-Rit1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480572	F	MP:0001293	anophthalmia	Rit1<em1(IMPC)Mbp>/Rit1<em1(IMPC)Mbp>	C57BL/6N-Rit1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480572	M	MP:0005343	increased circulating aspartate transaminase level	Rit1<em1(IMPC)Mbp>/Rit1<em1(IMPC)Mbp>	C57BL/6N-Rit1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480572	M	MP:0003068	enlarged kidney	Rit1<em1(IMPC)Mbp>/Rit1<em1(IMPC)Mbp>	C57BL/6N-Rit1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480573	M	MP:0009552	urinary bladder obstruction	Rnase11<em1(IMPC)Mbp>/Rnase11<em1(IMPC)Mbp>	C57BL/6N-Rnase11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480573	M	MP:0000266	abnormal heart morphology	Rnase11<em1(IMPC)Mbp>/Rnase11<em1(IMPC)Mbp>	C57BL/6N-Rnase11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480573	F	MP:0000692	small spleen	Rnase11<em1(IMPC)Mbp>/Rnase11<em1(IMPC)Mbp>	C57BL/6N-Rnase11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480573	F	MP:0000691	enlarged spleen	Rnase11<em1(IMPC)Mbp>/Rnase11<em1(IMPC)Mbp>	C57BL/6N-Rnase11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480573	F	MP:0000702	enlarged lymph nodes	Rnase11<em1(IMPC)Mbp>/Rnase11<em1(IMPC)Mbp>	C57BL/6N-Rnase11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480573	F	MP:0005013	increased lymphocyte cell number	Rnase11<em1(IMPC)Mbp>/Rnase11<em1(IMPC)Mbp>	C57BL/6N-Rnase11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480573	F	MP:0003918	decreased kidney weight	Rnase11<em1(IMPC)Mbp>/Rnase11<em1(IMPC)Mbp>	C57BL/6N-Rnase11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480573	F	MP:0002989	small kidney	Rnase11<em1(IMPC)Mbp>/Rnase11<em1(IMPC)Mbp>	C57BL/6N-Rnase11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480573	M	MP:0002188	small heart	Rnase11<em1(IMPC)Mbp>/Rnase11<em1(IMPC)Mbp>	C57BL/6N-Rnase11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480573	F	MP:0000689	abnormal spleen morphology	Rnase11<em1(IMPC)Mbp>/Rnase11<em1(IMPC)Mbp>	C57BL/6N-Rnase11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480573	F	MP:0002339	abnormal lymph node morphology	Rnase11<em1(IMPC)Mbp>/Rnase11<em1(IMPC)Mbp>	C57BL/6N-Rnase11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480576	M	MP:0003068	enlarged kidney	Rpl12<em1(IMPC)Mbp>/Rpl12<+>	C57BL/6NCrl-Rpl12<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480576	M	MP:0002339	abnormal lymph node morphology	Rpl12<em1(IMPC)Mbp>/Rpl12<+>	C57BL/6NCrl-Rpl12<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480576	M	MP:0000598	abnormal liver morphology	Rpl12<em1(IMPC)Mbp>/Rpl12<+>	C57BL/6NCrl-Rpl12<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480576	M	MP:0001157	small seminal vesicle	Rpl12<em1(IMPC)Mbp>/Rpl12<+>	C57BL/6NCrl-Rpl12<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480576	F	MP:0000274	enlarged heart	Rpl12<em1(IMPC)Mbp>/Rpl12<+>	C57BL/6NCrl-Rpl12<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480576	M	MP:0000702	enlarged lymph nodes	Rpl12<em1(IMPC)Mbp>/Rpl12<+>	C57BL/6NCrl-Rpl12<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480576	M	MP:0002059	abnormal seminal vesicle morphology	Rpl12<em1(IMPC)Mbp>/Rpl12<+>	C57BL/6NCrl-Rpl12<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480576	M	MP:0002092	abnormal eye morphology	Rpl12<em1(IMPC)Mbp>/Rpl12<+>	C57BL/6NCrl-Rpl12<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480578	F	MP:0001566	increased circulating phosphate level	Rsad2<em1(IMPC)H>/Rsad2<em1(IMPC)H>	C57BL/6NTac-Rsad2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6480578	F	MP:0020870	decreased thigmotaxis	Rsad2<em1(IMPC)H>/Rsad2<em1(IMPC)H>	C57BL/6NTac-Rsad2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6480578	F	MP:0005627	increased circulating potassium level	Rsad2<em1(IMPC)H>/Rsad2<em1(IMPC)H>	C57BL/6NTac-Rsad2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6480578	F	MP:0005553	increased circulating creatinine level	Rsad2<em1(IMPC)H>/Rsad2<em1(IMPC)H>	C57BL/6NTac-Rsad2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6480578	F	MP:0004924	abnormal behavior	Rsad2<em1(IMPC)H>/Rsad2<em1(IMPC)H>	C57BL/6NTac-Rsad2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6480578	F	MP:0001402	decreased locomotor activity	Rsad2<em1(IMPC)H>/Rsad2<em1(IMPC)H>	C57BL/6NTac-Rsad2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6480578	M	MP:0002965	increased circulating serum albumin level	Rsad2<em1(IMPC)H>/Rsad2<em1(IMPC)H>	C57BL/6NTac-Rsad2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6480579	F	MP:0003717	pallor	Rsu1<em1(IMPC)J>/Rsu1<em1(IMPC)J>	C57BL/6NJ-Rsu1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480581	M	MP:0000266	abnormal heart morphology	Septin6<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Septin6<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480581	M	MP:0002968	increased circulating alkaline phosphatase level	Septin6<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Septin6<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480581	M	MP:0000274	enlarged heart	Septin6<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Septin6<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480582	F	MP:0000274	enlarged heart	Septin6<tm1.1(KOMP)Vlcg>/Septin6<tm1.1(KOMP)Vlcg>	C57BL/6N-Septin6<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480582	F	MP:0000266	abnormal heart morphology	Septin6<tm1.1(KOMP)Vlcg>/Septin6<tm1.1(KOMP)Vlcg>	C57BL/6N-Septin6<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480586	M	MP:0001925	male infertility	Slc25a42<em1(IMPC)J>/Slc25a42<em1(IMPC)J>	C57BL/6NJ-Slc25a42<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480588	F	MP:0001402	decreased locomotor activity	Slc46a1<tm1b(KOMP)Mbp>/Slc46a1<tm1b(KOMP)Mbp>	C57BL/6N-Slc46a1<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:6480589	M	MP:0001711	abnormal placenta morphology	Slit2<em1(IMPC)Mbp>/Slit2<em1(IMPC)Mbp>	C57BL/6N-Slit2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480590	M	MP:0002059	abnormal seminal vesicle morphology	Snd1<em1(IMPC)Tcp>/Snd1<+>	C57BL/6NCrl-Snd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480590	F	MP:0002637	small uterus	Snd1<em1(IMPC)Tcp>/Snd1<+>	C57BL/6NCrl-Snd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480590	F	MP:0004953	decreased spleen weight	Snd1<em1(IMPC)Tcp>/Snd1<+>	C57BL/6NCrl-Snd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480590	M	MP:0000706	small thymus	Snd1<em1(IMPC)Tcp>/Snd1<+>	C57BL/6NCrl-Snd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480590	M	MP:0000219	increased neutrophil cell number	Snd1<em1(IMPC)Tcp>/Snd1<+>	C57BL/6NCrl-Snd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480590	M	MP:0011874	enlarged urinary bladder	Snd1<em1(IMPC)Tcp>/Snd1<+>	C57BL/6NCrl-Snd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480590	F	MP:0000157	abnormal sternum morphology	Snd1<em1(IMPC)Tcp>/Snd1<+>	C57BL/6NCrl-Snd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480590	M	MP:0005016	decreased lymphocyte cell number	Snd1<em1(IMPC)Tcp>/Snd1<+>	C57BL/6NCrl-Snd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480590	M	MP:0002941	increased circulating alanine transaminase level	Snd1<em1(IMPC)Tcp>/Snd1<+>	C57BL/6NCrl-Snd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480591	F	MP:0005011	increased eosinophil cell number	Spata2<tm1.1(KOMP)Vlcg>/Spata2<tm1.1(KOMP)Vlcg>	C57BL/6N-Spata2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6480591	F	MP:0005016	decreased lymphocyte cell number	Spata2<tm1.1(KOMP)Vlcg>/Spata2<tm1.1(KOMP)Vlcg>	C57BL/6N-Spata2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6480595	F	MP:0000157	abnormal sternum morphology	Sspo<em8(IMPC)Tcp>/Sspo<em8(IMPC)Tcp>	C57BL/6N-Sspo<em8(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480595	F	MP:0002092	abnormal eye morphology	Sspo<em8(IMPC)Tcp>/Sspo<em8(IMPC)Tcp>	C57BL/6N-Sspo<em8(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480595	F	MP:0001120	abnormal uterus morphology	Sspo<em8(IMPC)Tcp>/Sspo<em8(IMPC)Tcp>	C57BL/6N-Sspo<em8(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6480596	F	MP:0020870	decreased thigmotaxis	Ssu72<em1(IMPC)J>/Ssu72<+>	C57BL/6NJ-Ssu72<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480597	F	MP:0000689	abnormal spleen morphology	Stag1<em1(IMPC)Mbp>/Stag1<+>	C57BL/6N-Stag1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480597	M	MP:0002997	enlarged seminal vesicle	Stag1<em1(IMPC)Mbp>/Stag1<+>	C57BL/6N-Stag1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480597	M	MP:0001552	increased circulating triglyceride level	Stag1<em1(IMPC)Mbp>/Stag1<+>	C57BL/6N-Stag1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480597	M	MP:0000692	small spleen	Stag1<em1(IMPC)Mbp>/Stag1<+>	C57BL/6N-Stag1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480597	F	MP:0000702	enlarged lymph nodes	Stag1<em1(IMPC)Mbp>/Stag1<+>	C57BL/6N-Stag1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480597	F	MP:0000691	enlarged spleen	Stag1<em1(IMPC)Mbp>/Stag1<+>	C57BL/6N-Stag1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480597	F	MP:0002989	small kidney	Stag1<em1(IMPC)Mbp>/Stag1<+>	C57BL/6N-Stag1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480597	F	MP:0002135	abnormal kidney morphology	Stag1<em1(IMPC)Mbp>/Stag1<+>	C57BL/6N-Stag1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480597	F	MP:0009084	blind uterus	Stag1<em1(IMPC)Mbp>/Stag1<+>	C57BL/6N-Stag1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480597	M	MP:0009552	urinary bladder obstruction	Stag1<em1(IMPC)Mbp>/Stag1<+>	C57BL/6N-Stag1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480597	F	MP:0002339	abnormal lymph node morphology	Stag1<em1(IMPC)Mbp>/Stag1<+>	C57BL/6N-Stag1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480597	F	MP:0001297	microphthalmia	Stag1<em1(IMPC)Mbp>/Stag1<+>	C57BL/6N-Stag1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480601	M	MP:0002968	increased circulating alkaline phosphatase level	Taok2<tm1b(EUCOMM)Hmgu>/Taok2<+>	C57BL/6N-Taok2<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6480603	M	MP:0001556	increased circulating HDL cholesterol level	Tbx22<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Tbx22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6480606	M	MP:0002599	increased mean platelet volume	Tceal9<tm1a(KOMP)Wtsi>/Y	C57BL/6N-Tceal9<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6480606	M	MP:0010067	increased red blood cell distribution width	Tceal9<tm1a(KOMP)Wtsi>/Y	C57BL/6N-Tceal9<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6480611	M	MP:0010088	decreased circulating fructosamine level	Tmco2<tm1a(KOMP)Wtsi>/Tmco2<tm1a(KOMP)Wtsi>	C57BL/6N-Tmco2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6480612	M	MP:0000062	increased bone mineral density	Tmco3<tm1b(KOMP)Wtsi>/Tmco3<tm1b(KOMP)Wtsi>	C57BL/6N-Tmco3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6480612	F	MP:0001488	increased startle reflex	Tmco3<tm1b(KOMP)Wtsi>/Tmco3<tm1b(KOMP)Wtsi>	C57BL/6N-Tmco3<tm1b(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6480617	M	MP:0005576	decreased pulmonary ventilation	Trappc2<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Trappc2<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480617	M	MP:0005575	increased pulmonary ventilation	Trappc2<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Trappc2<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480617	M	MP:0012125	decreased bronchoconstrictive response	Trappc2<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Trappc2<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480618	F	MP:0005576	decreased pulmonary ventilation	Trappc2<tm1.1(KOMP)Vlcg>/Trappc2<tm1.1(KOMP)Vlcg>	C57BL/6N-Trappc2<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6480621	F	MP:0001566	increased circulating phosphate level	Trmt10b<em1(IMPC)J>/Trmt10b<em1(IMPC)J>	C57BL/6NJ-Trmt10b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480621	F	MP:0001284	absent vibrissae	Trmt10b<em1(IMPC)J>/Trmt10b<em1(IMPC)J>	C57BL/6NJ-Trmt10b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480628	M	MP:0005011	increased eosinophil cell number	Usp16<tm1b(EUCOMM)Hmgu>/Usp16<+>	C57BL/6N-Usp16<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:6480628	M	MP:0002606	increased basophil cell number	Usp16<tm1b(EUCOMM)Hmgu>/Usp16<+>	C57BL/6N-Usp16<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:6480629	M	MP:0001402	decreased locomotor activity	Vsig4<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480629	M	MP:0005560	decreased circulating glucose level	Vsig4<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480629	M	MP:0005343	increased circulating aspartate transaminase level	Vsig4<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480629	M	MP:0002941	increased circulating alanine transaminase level	Vsig4<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480629	M	MP:0010025	decreased total body fat amount	Vsig4<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480629	M	MP:0003960	increased lean body mass	Vsig4<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480629	M	MP:0002959	increased urine microalbumin level	Vsig4<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480629	M	MP:0002968	increased circulating alkaline phosphatase level	Vsig4<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480629	M	MP:0005562	decreased mean corpuscular hemoglobin	Vsig4<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480629	M	MP:0005627	increased circulating potassium level	Vsig4<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480629	M	MP:0005278	abnormal cholesterol homeostasis	Vsig4<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Vsig4<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6480630	M	MP:0013279	increased fasting circulating glucose level	Washc4<em1(IMPC)J>/Washc4<+>	C57BL/6NJ-Washc4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480639	F	MP:0000702	enlarged lymph nodes	Yy2<em1(IMPC)Mbp>/Yy2<em1(IMPC)Mbp>	C57BL/6NCrl-Yy2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480639	F	MP:0002092	abnormal eye morphology	Yy2<em1(IMPC)Mbp>/Yy2<em1(IMPC)Mbp>	C57BL/6NCrl-Yy2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480639	F	MP:0002339	abnormal lymph node morphology	Yy2<em1(IMPC)Mbp>/Yy2<em1(IMPC)Mbp>	C57BL/6NCrl-Yy2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480639	F	MP:0001293	anophthalmia	Yy2<em1(IMPC)Mbp>/Yy2<em1(IMPC)Mbp>	C57BL/6NCrl-Yy2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6480641	F	MP:0000367	abnormal coat/ hair morphology	Zc3h13<em1(IMPC)J>/Zc3h13<+>	C57BL/6NJ-Zc3h13<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480641	M	MP:0001556	increased circulating HDL cholesterol level	Zc3h13<em1(IMPC)J>/Zc3h13<+>	C57BL/6NJ-Zc3h13<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480641	M	MP:0002874	decreased hemoglobin content	Zc3h13<em1(IMPC)J>/Zc3h13<+>	C57BL/6NJ-Zc3h13<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480641	M	MP:0005178	increased circulating cholesterol level	Zc3h13<em1(IMPC)J>/Zc3h13<+>	C57BL/6NJ-Zc3h13<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480641	F	MP:0001529	abnormal vocalization	Zc3h13<em1(IMPC)J>/Zc3h13<+>	C57BL/6NJ-Zc3h13<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6480642	F	MP:0000186	decreased circulating HDL cholesterol level	Zfp182<tm1b(KOMP)Wtsi>/Zfp182<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp182<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6480643	F	MP:0003394	increased cardiac output	Zfp300<em1(IMPC)Bay>/Zfp300<em1(IMPC)Bay>	C57BL/6N-Zfp300<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480645	M	MP:0002968	increased circulating alkaline phosphatase level	Zfp469<em1(IMPC)Mbp>/Zfp469<em1(IMPC)Mbp>	C57BL/6N-Zfp469<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480645	M	MP:0001258	decreased body length	Zfp469<em1(IMPC)Mbp>/Zfp469<em1(IMPC)Mbp>	C57BL/6N-Zfp469<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480645	F	MP:0000218	increased leukocyte cell number	Zfp469<em1(IMPC)Mbp>/Zfp469<em1(IMPC)Mbp>	C57BL/6N-Zfp469<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480645	M	MP:0003068	enlarged kidney	Zfp469<em1(IMPC)Mbp>/Zfp469<em1(IMPC)Mbp>	C57BL/6N-Zfp469<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480645	M	MP:0002135	abnormal kidney morphology	Zfp469<em1(IMPC)Mbp>/Zfp469<em1(IMPC)Mbp>	C57BL/6N-Zfp469<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480645	M	MP:0002059	abnormal seminal vesicle morphology	Zfp469<em1(IMPC)Mbp>/Zfp469<em1(IMPC)Mbp>	C57BL/6N-Zfp469<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480645	F	MP:0005013	increased lymphocyte cell number	Zfp469<em1(IMPC)Mbp>/Zfp469<em1(IMPC)Mbp>	C57BL/6N-Zfp469<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6480646	F	MP:0011100	preweaning lethality, complete penetrance	Zfp654<em1(IMPC)Bay>/Zfp654<em1(IMPC)Bay>	C57BL/6N-Zfp654<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6480648	M	MP:0002135	abnormal kidney morphology	Zzef1<tm2.1(KOMP)Vlcg>/Zzef1<tm2.1(KOMP)Vlcg>	C57BL/6N-Zzef1<tm2.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6480648	F	MP:0002968	increased circulating alkaline phosphatase level	Zzef1<tm2.1(KOMP)Vlcg>/Zzef1<tm2.1(KOMP)Vlcg>	C57BL/6N-Zzef1<tm2.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6480648	M	MP:0003917	increased kidney weight	Zzef1<tm2.1(KOMP)Vlcg>/Zzef1<tm2.1(KOMP)Vlcg>	C57BL/6N-Zzef1<tm2.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6487965	F	MP:0005378	growth/size/body region phenotype	Gdpd2<tm1.1Soc>/Gdpd2<tm1.1Soc>	involves: 129/Sv * BALB/cJ * C57BL/6J	Y	31932351
MGI:6487965	F	MP:0000955	abnormal spinal cord morphology	Gdpd2<tm1.1Soc>/Gdpd2<tm1.1Soc>	involves: 129/Sv * BALB/cJ * C57BL/6J	N	31932351
MGI:6487965	F	MP:0020393	increased neuronal precursor proliferation	Gdpd2<tm1.1Soc>/Gdpd2<tm1.1Soc>	involves: 129/Sv * BALB/cJ * C57BL/6J	N	31932351
MGI:6487965	F	MP:0005389	reproductive system phenotype	Gdpd2<tm1.1Soc>/Gdpd2<tm1.1Soc>	involves: 129/Sv * BALB/cJ * C57BL/6J	Y	31932351
MGI:6487965	F	MP:0003077	abnormal cell cycle	Gdpd2<tm1.1Soc>/Gdpd2<tm1.1Soc>	involves: 129/Sv * BALB/cJ * C57BL/6J	N	31932351
MGI:6487966	M	MP:0005378	growth/size/body region phenotype	Gdpd2<tm1.1Soc>/Y	involves: 129/Sv * BALB/cJ * C57BL/6J	Y	31932351
MGI:6487966	M	MP:0005389	reproductive system phenotype	Gdpd2<tm1.1Soc>/Y	involves: 129/Sv * BALB/cJ * C57BL/6J	Y	31932351
MGI:6487966	M	MP:0003077	abnormal cell cycle	Gdpd2<tm1.1Soc>/Y	involves: 129/Sv * BALB/cJ * C57BL/6J	N	31932351
MGI:6487966	M	MP:0000955	abnormal spinal cord morphology	Gdpd2<tm1.1Soc>/Y	involves: 129/Sv * BALB/cJ * C57BL/6J	N	31932351
MGI:6487966	M	MP:0020393	increased neuronal precursor proliferation	Gdpd2<tm1.1Soc>/Y	involves: 129/Sv * BALB/cJ * C57BL/6J	N	31932351
MGI:6487970	F	MP:0010892	increased oligodendrocyte progenitor number	Gdpd2<tm1.1Soc>/Gdpd2<+>,Hprt1<tm1(CMV-GFP)Nat>/Hprt1<+>	involves: 129/Sv * 129P2 /SvPas * 129S * BALB/cJ * C57BL/6J	N	31932351
MGI:6487970	F	MP:0010160	increased oligodendrocyte number	Gdpd2<tm1.1Soc>/Gdpd2<+>,Hprt1<tm1(CMV-GFP)Nat>/Hprt1<+>	involves: 129/Sv * 129P2 /SvPas * 129S * BALB/cJ * C57BL/6J	N	31932351
MGI:6488168	M	MP:0005389	reproductive system phenotype	Fbxl13<em1Osb>/Fbxl13<em1Osb>	involves: C57BL/6NSlc * DBA/2	Y	31961863
MGI:6488169	M	MP:0001156	abnormal spermatogenesis	Drc7<tm1.1Osb>/Drc7<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	31961863
MGI:6488169	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Drc7<tm1.1Osb>/Drc7<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	31961863
MGI:6488169	M	MP:0020869	immotile sperm	Drc7<tm1.1Osb>/Drc7<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	31961863
MGI:6488169	M	MP:0001147	small testis	Drc7<tm1.1Osb>/Drc7<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	31961863
MGI:6488169	M	MP:0009838	abnormal sperm axoneme morphology	Drc7<tm1.1Osb>/Drc7<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	31961863
MGI:6488169	M	MP:0009376	abnormal manchette morphology	Drc7<tm1.1Osb>/Drc7<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	31961863
MGI:6488169	M	MP:0009239	short sperm flagellum	Drc7<tm1.1Osb>/Drc7<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	31961863
MGI:6488169	M	MP:0006380	abnormal spermatid morphology	Drc7<tm1.1Osb>/Drc7<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	31961863
MGI:6488169	M	MP:0009230	abnormal sperm head morphology	Drc7<tm1.1Osb>/Drc7<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	31961863
MGI:6488169	M	MP:0002687	oligozoospermia	Drc7<tm1.1Osb>/Drc7<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	31961863
MGI:6488169	M	MP:0001925	male infertility	Drc7<tm1.1Osb>/Drc7<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	31961863
MGI:6488169	M	MP:0008892	abnormal sperm flagellum morphology	Drc7<tm1.1Osb>/Drc7<tm1.1Osb>	involves: C57BL/6NSlc * DBA/2	N	31961863
MGI:6488170	M	MP:0008261	arrest of male meiosis	Meiosin<em1Keish>/Meiosin<em1Keish>	involves: C57BL/6 * C57BL/6N	N	32032549
MGI:6488170	F	MP:0005168	abnormal female meiosis	Meiosin<em1Keish>/Meiosin<em1Keish>	involves: C57BL/6 * C57BL/6N	N	32032549
MGI:6488170	F	MP:0008967	absent chiasmata formation	Meiosin<em1Keish>/Meiosin<em1Keish>	involves: C57BL/6 * C57BL/6N	N	32032549
MGI:6488170	F	MP:0002682	decreased mature ovarian follicle number	Meiosin<em1Keish>/Meiosin<em1Keish>	involves: C57BL/6 * C57BL/6N	N	32032549
MGI:6488170	M	MP:0001940	testis hypoplasia	Meiosin<em1Keish>/Meiosin<em1Keish>	involves: C57BL/6 * C57BL/6N	N	32032549
MGI:6488170	F	MP:0009452	abnormal synaptonemal complex	Meiosin<em1Keish>/Meiosin<em1Keish>	involves: C57BL/6 * C57BL/6N	N	32032549
MGI:6488170	M	MP:0005159	azoospermia	Meiosin<em1Keish>/Meiosin<em1Keish>	involves: C57BL/6 * C57BL/6N	N	32032549
MGI:6488170	F	MP:0013236	ovary degeneration	Meiosin<em1Keish>/Meiosin<em1Keish>	involves: C57BL/6 * C57BL/6N	N	32032549
MGI:6488170	M	MP:0005169	abnormal male meiosis	Meiosin<em1Keish>/Meiosin<em1Keish>	involves: C57BL/6 * C57BL/6N	N	32032549
MGI:6488170	F	MP:0009564	abnormal meiotic configurations	Meiosin<em1Keish>/Meiosin<em1Keish>	involves: C57BL/6 * C57BL/6N	N	32032549
MGI:6488170	M	MP:0014052	increased male germ cell apoptosis	Meiosin<em1Keish>/Meiosin<em1Keish>	involves: C57BL/6 * C57BL/6N	N	32032549
MGI:6488170	F	MP:0010767	abnormal female meiosis I arrest	Meiosin<em1Keish>/Meiosin<em1Keish>	involves: C57BL/6 * C57BL/6N	N	32032549
MGI:6488171	M	MP:0005169	abnormal male meiosis	Stra8<em4Keish>/Stra8<em4Keish>	involves: 129S6/SvEvTac * C57BL/6J	N	32032549
MGI:6488171	M	MP:0005159	azoospermia	Stra8<em4Keish>/Stra8<em4Keish>	involves: 129S6/SvEvTac * C57BL/6J	N	32032549
MGI:6488171	M	MP:0008261	arrest of male meiosis	Stra8<em4Keish>/Stra8<em4Keish>	involves: 129S6/SvEvTac * C57BL/6J	N	32032549
MGI:6488175	M	MP:0012307	impaired spatial learning	Kcnq2<tm1.1Lvi>/Kcnq2<+>	129-Kcnq2<tm1.1Lvi>/Lvi	N	32239694
MGI:6488175	M	MP:0000434	megacephaly	Kcnq2<tm1.1Lvi>/Kcnq2<+>	129-Kcnq2<tm1.1Lvi>/Lvi	N	32239694
MGI:6488175	M	MP:0012443	increased corpus callosum size	Kcnq2<tm1.1Lvi>/Kcnq2<+>	129-Kcnq2<tm1.1Lvi>/Lvi	N	32239694
MGI:6488175	M	MP:0000905	increased superior colliculus size	Kcnq2<tm1.1Lvi>/Kcnq2<+>	129-Kcnq2<tm1.1Lvi>/Lvi	N	32239694
MGI:6488175	M	MP:0001417	decreased exploration in new environment	Kcnq2<tm1.1Lvi>/Kcnq2<+>	129-Kcnq2<tm1.1Lvi>/Lvi	N	32239694
MGI:6488598	M	MP:0001925	male infertility	Mettl5<em1Schne>/Mettl5<em1Schne>	involves: C57BL/6NCrl	N	32217665
MGI:6488598	M	MP:0006378	abnormal spermatogonia morphology	Mettl5<em1Schne>/Mettl5<em1Schne>	involves: C57BL/6NCrl	N	32217665
MGI:6488598	M	MP:0001154	seminiferous tubule degeneration	Mettl5<em1Schne>/Mettl5<em1Schne>	involves: C57BL/6NCrl	N	32217665
MGI:6489966	M	MP:0001922	reduced male fertility	Ano5<em1Huyi>/Ano5<em1Huyi>	C57BL/6N-Ano5<em1Huyi>	N	30712070
MGI:6489988	M	MP:0001925	male infertility	Prdm9<em2Kpgn>/Prdm9<em2Kpgn>	C57BL/6J-Prdm9<em2Kpgn>/Kpgn	N	33097538
MGI:6489988	F	MP:0005431	decreased oocyte number	Prdm9<em2Kpgn>/Prdm9<em2Kpgn>	C57BL/6J-Prdm9<em2Kpgn>/Kpgn	N	33097538
MGI:6489988	F	MP:0001127	small ovary	Prdm9<em2Kpgn>/Prdm9<em2Kpgn>	C57BL/6J-Prdm9<em2Kpgn>/Kpgn	N	33097538
MGI:6489988	F	MP:0009451	abnormal chromosomal synapsis	Prdm9<em2Kpgn>/Prdm9<em2Kpgn>	C57BL/6J-Prdm9<em2Kpgn>/Kpgn	N	33097538
MGI:6489988	F	MP:0008966	abnormal chiasmata formation	Prdm9<em2Kpgn>/Prdm9<em2Kpgn>	C57BL/6J-Prdm9<em2Kpgn>/Kpgn	N	33097538
MGI:6489988	M	MP:0008878	abnormal DNA methylation during gametogenesis	Prdm9<em2Kpgn>/Prdm9<em2Kpgn>	C57BL/6J-Prdm9<em2Kpgn>/Kpgn	N	33097538
MGI:6489988	F	MP:0001923	reduced female fertility	Prdm9<em2Kpgn>/Prdm9<em2Kpgn>	C57BL/6J-Prdm9<em2Kpgn>/Kpgn	N	33097538
MGI:6489988	F	MP:0005168	abnormal female meiosis	Prdm9<em2Kpgn>/Prdm9<em2Kpgn>	C57BL/6J-Prdm9<em2Kpgn>/Kpgn	N	33097538
MGI:6489988	M	MP:0008261	arrest of male meiosis	Prdm9<em2Kpgn>/Prdm9<em2Kpgn>	C57BL/6J-Prdm9<em2Kpgn>/Kpgn	N	33097538
MGI:6490002	F	MP:0005431	decreased oocyte number	Prdm9<em2Kpgn>/Prdm9<+>	C57BL/6J-Prdm9<em2Kpgn>/Kpgn	N	33097538
MGI:6490362	F	MP:0005397	hematopoietic system phenotype	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Stag2<tm1.1Alos>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490362	F	MP:0013501	increased fibroblast apoptosis	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Stag2<tm1.1Alos>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490362	F	MP:0010763	abnormal hematopoietic stem cell physiology	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Stag2<tm1.1Alos>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490362	F	MP:0011704	decreased fibroblast proliferation	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Stag2<tm1.1Alos>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490362	F	MP:0000316	cellular necrosis	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Stag2<tm1.1Alos>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490362	F	MP:0002006	neoplasm	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Stag2<tm1.1Alos>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490362	F	MP:0008883	abnormal enterocyte proliferation	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Stag2<tm1.1Alos>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490362	F	MP:0000477	abnormal intestine morphology	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Stag2<tm1.1Alos>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490362	F	MP:0001262	decreased body weight	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Stag2<tm1.1Alos>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490362	F	MP:0002083	premature death	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Stag2<tm1.1Alos>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490362	F	MP:0004046	abnormal mitosis	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Stag2<tm1.1Alos>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490363	M	MP:0001262	decreased body weight	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Y	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490363	M	MP:0002006	neoplasm	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Y	involves: 129S6/SvEvTac * C57BL/6NCrl	Y	32783938
MGI:6490363	M	MP:0005397	hematopoietic system phenotype	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Y	involves: 129S6/SvEvTac * C57BL/6NCrl	Y	32783938
MGI:6490363	M	MP:0000477	abnormal intestine morphology	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Y	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490363	M	MP:0002083	premature death	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Y	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490363	M	MP:0010763	abnormal hematopoietic stem cell physiology	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Y	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490363	M	MP:0004046	abnormal mitosis	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Y	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490363	M	MP:0011704	decreased fibroblast proliferation	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Y	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490363	M	MP:0000316	cellular necrosis	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Y	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490363	M	MP:0008883	abnormal enterocyte proliferation	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Y	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490363	M	MP:0013501	increased fibroblast apoptosis	Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>,Stag2<tm1.1Alos>/Y	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490364	M	MP:0001698	decreased embryo size	Stag2<tm1.1Alos>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490364	M	MP:0011098	embryonic lethality during organogenesis, complete penetrance	Stag2<tm1.1Alos>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490364	M	MP:0010406	common atrium	Stag2<tm1.1Alos>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490364	M	MP:0003649	decreased heart right ventricle size	Stag2<tm1.1Alos>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490364	M	MP:0000352	decreased cell proliferation	Stag2<tm1.1Alos>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490364	M	MP:0000267	abnormal heart development	Stag2<tm1.1Alos>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490364	M	MP:0003984	embryonic growth retardation	Stag2<tm1.1Alos>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490364	M	MP:0006126	abnormal cardiac outflow tract development	Stag2<tm1.1Alos>/Y,Tg(CAG-cre)1Nagy/0	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32783938
MGI:6490650	M	MP:0008261	arrest of male meiosis	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	C3.129P2(B6)-Prdm9<tm1Ymat>/HandJ	N	33097538
MGI:6490650	F	MP:0005168	abnormal female meiosis	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	C3.129P2(B6)-Prdm9<tm1Ymat>/HandJ	N	33097538
MGI:6490650	F	MP:0005431	decreased oocyte number	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	C3.129P2(B6)-Prdm9<tm1Ymat>/HandJ	N	33097538
MGI:6490650	F	MP:0001926	female infertility	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	C3.129P2(B6)-Prdm9<tm1Ymat>/HandJ	N	33097538
MGI:6490650	M	MP:0001925	male infertility	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	C3.129P2(B6)-Prdm9<tm1Ymat>/HandJ	N	33097538
MGI:6491489	F	MP:0009619	abnormal optokinetic reflex	Frmd7<tm1b(KOMP)Wtsi>/Frmd7<tm1b(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	33007925
MGI:6491489	F	MP:0005391	vision/eye phenotype	Frmd7<tm1b(KOMP)Wtsi>/Frmd7<tm1b(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	Y	33007925
MGI:6491490	M	MP:0005391	vision/eye phenotype	Frmd7<tm1b(KOMP)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	Y	33007925
MGI:6491490	M	MP:0009619	abnormal optokinetic reflex	Frmd7<tm1b(KOMP)Wtsi>/Y	involves: C57BL/6 * C57BL/6N	N	33007925
MGI:6491898	F	MP:0001926	female infertility	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * FVB	N	32943573
MGI:6491898	M	MP:0013600	testis degeneration	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * FVB	N	32943573
MGI:6491898	M	MP:0001147	small testis	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * FVB	N	32943573
MGI:6491898	M	MP:0001925	male infertility	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * FVB	N	32943573
MGI:6491898	F	MP:0001126	abnormal ovary morphology	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * FVB	N	32943573
MGI:6491901	M	MP:0002687	oligozoospermia	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * FVB/NJ	N	32943573
MGI:6491901	M	MP:0001147	small testis	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * FVB/NJ	N	32943573
MGI:6491901	M	MP:0001922	reduced male fertility	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * FVB/NJ	N	32943573
MGI:6491901	M	MP:0001154	seminiferous tubule degeneration	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * FVB/NJ	N	32943573
MGI:6491904	M	MP:0005389	reproductive system phenotype	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Prm-cre)58Og/0	involves: 129S4/SvJae * 129S4/SvJaeSor * BALB/c * C57BL/6	Y	32943573
MGI:6491906	F	MP:0001926	female infertility	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Zp3-cre)93Knw/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * C57BL/6J	N	32943573
MGI:6491906	F	MP:0001125	abnormal oocyte morphology	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Zp3-cre)93Knw/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * C57BL/6J	N	32943573
MGI:6491906	F	MP:0005168	abnormal female meiosis	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Zp3-cre)93Knw/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * C57BL/6J	N	32943573
MGI:6491906	F	MP:0005431	decreased oocyte number	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Zp3-cre)93Knw/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * C57BL/6J	N	32943573
MGI:6491906	F	MP:0005379	endocrine/exocrine gland phenotype	Mettl3<tm1.1Jhha>/Mettl3<tm1.1Jhha>,Tg(Zp3-cre)93Knw/0	involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * C57BL/6J	Y	32943573
MGI:6491912	F	MP:0001926	female infertility	Ythdf2<em2Jhha>/Ythdf2<em2Jhha>	involves: BALB/c * C57BL/6	N	32943573
MGI:6491912	M	MP:0002784	abnormal Sertoli cell morphology	Ythdf2<em2Jhha>/Ythdf2<em2Jhha>	involves: BALB/c * C57BL/6	N	32943573
MGI:6491912	F	MP:0005389	reproductive system phenotype	Ythdf2<em2Jhha>/Ythdf2<em2Jhha>	involves: BALB/c * C57BL/6	Y	32943573
MGI:6491912	M	MP:0002687	oligozoospermia	Ythdf2<em2Jhha>/Ythdf2<em2Jhha>	involves: BALB/c * C57BL/6	N	32943573
MGI:6491912	M	MP:0001922	reduced male fertility	Ythdf2<em2Jhha>/Ythdf2<em2Jhha>	involves: BALB/c * C57BL/6	N	32943573
MGI:6491912	M	MP:0001154	seminiferous tubule degeneration	Ythdf2<em2Jhha>/Ythdf2<em2Jhha>	involves: BALB/c * C57BL/6	N	32943573
MGI:6492211	M	MP:0002797	increased thigmotaxis	Lrrc7<Tg(Myl2-TSPYL)1Sich>/Lrrc7<Tg(Myl2-TSPYL)1Sich>	involves: FVB/N	N	31582721
MGI:6492211	M	MP:0001360	abnormal social investigation	Lrrc7<Tg(Myl2-TSPYL)1Sich>/Lrrc7<Tg(Myl2-TSPYL)1Sich>	involves: FVB/N	N	31582721
MGI:6492211	M	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology	Lrrc7<Tg(Myl2-TSPYL)1Sich>/Lrrc7<Tg(Myl2-TSPYL)1Sich>	involves: FVB/N	N	31582721
MGI:6492211	M	MP:0008428	abnormal spatial working memory	Lrrc7<Tg(Myl2-TSPYL)1Sich>/Lrrc7<Tg(Myl2-TSPYL)1Sich>	involves: FVB/N	N	31582721
MGI:6492211	M	MP:0008415	abnormal neurite morphology	Lrrc7<Tg(Myl2-TSPYL)1Sich>/Lrrc7<Tg(Myl2-TSPYL)1Sich>	involves: FVB/N	N	31582721
MGI:6492211	M	MP:0001353	increased aggression towards mice	Lrrc7<Tg(Myl2-TSPYL)1Sich>/Lrrc7<Tg(Myl2-TSPYL)1Sich>	involves: FVB/N	N	31582721
MGI:6492227	M	MP:0002797	increased thigmotaxis	Lrrc7<Tg(Myl2-TSPYL)1Sich>/Lrrc7<+>	involves: FVB/N	N	31582721
MGI:6492227	M	MP:0001360	abnormal social investigation	Lrrc7<Tg(Myl2-TSPYL)1Sich>/Lrrc7<+>	involves: FVB/N	N	31582721
MGI:6492674	F	MP:0002060	abnormal skin morphology	2610008E11Rik<em1(IMPC)Mbp>/2610008E11Rik<em1(IMPC)Mbp>	C57BL/6N-2610008E11Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492674	F	MP:0002188	small heart	2610008E11Rik<em1(IMPC)Mbp>/2610008E11Rik<em1(IMPC)Mbp>	C57BL/6N-2610008E11Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492674	F	MP:0000266	abnormal heart morphology	2610008E11Rik<em1(IMPC)Mbp>/2610008E11Rik<em1(IMPC)Mbp>	C57BL/6N-2610008E11Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492674	M	MP:0002135	abnormal kidney morphology	2610008E11Rik<em1(IMPC)Mbp>/2610008E11Rik<em1(IMPC)Mbp>	C57BL/6N-2610008E11Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492674	M	MP:0003068	enlarged kidney	2610008E11Rik<em1(IMPC)Mbp>/2610008E11Rik<em1(IMPC)Mbp>	C57BL/6N-2610008E11Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492676	F	MP:0001402	decreased locomotor activity	4930524B15Rik<em1(IMPC)Mbp>/4930524B15Rik<em1(IMPC)Mbp>	C57BL/6NCrl-4930524B15Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492676	M	MP:0005084	abnormal gallbladder morphology	4930524B15Rik<em1(IMPC)Mbp>/4930524B15Rik<em1(IMPC)Mbp>	C57BL/6NCrl-4930524B15Rik<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492677	F	MP:0005292	improved glucose tolerance	4933402J07Rik<em1(IMPC)J>/4933402J07Rik<em1(IMPC)J>	C57BL/6NJ-4933402J07Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492677	M	MP:0001392	abnormal locomotor behavior	4933402J07Rik<em1(IMPC)J>/4933402J07Rik<em1(IMPC)J>	C57BL/6NJ-4933402J07Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492678	M	MP:0002941	increased circulating alanine transaminase level	Aasdh<em1(IMPC)Tcp>/Aasdh<em1(IMPC)Tcp>	C57BL/6N-Aasdh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492678	M	MP:0002092	abnormal eye morphology	Aasdh<em1(IMPC)Tcp>/Aasdh<em1(IMPC)Tcp>	C57BL/6N-Aasdh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492678	M	MP:0000157	abnormal sternum morphology	Aasdh<em1(IMPC)Tcp>/Aasdh<em1(IMPC)Tcp>	C57BL/6N-Aasdh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492679	F	MP:0005560	decreased circulating glucose level	Abcb4<em1(IMPC)H>/Abcb4<em1(IMPC)H>	C57BL/6NTac-Abcb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492679	F	MP:0010067	increased red blood cell distribution width	Abcb4<em1(IMPC)H>/Abcb4<em1(IMPC)H>	C57BL/6NTac-Abcb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492679	F	MP:0000186	decreased circulating HDL cholesterol level	Abcb4<em1(IMPC)H>/Abcb4<em1(IMPC)H>	C57BL/6NTac-Abcb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492679	F	MP:0005344	increased circulating bilirubin level	Abcb4<em1(IMPC)H>/Abcb4<em1(IMPC)H>	C57BL/6NTac-Abcb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492679	M	MP:0008806	increased circulating amylase level	Abcb4<em1(IMPC)H>/Abcb4<em1(IMPC)H>	C57BL/6NTac-Abcb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492679	F	MP:0002874	decreased hemoglobin content	Abcb4<em1(IMPC)H>/Abcb4<em1(IMPC)H>	C57BL/6NTac-Abcb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492679	M	MP:0000220	increased monocyte cell number	Abcb4<em1(IMPC)H>/Abcb4<em1(IMPC)H>	C57BL/6NTac-Abcb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492679	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Abcb4<em1(IMPC)H>/Abcb4<em1(IMPC)H>	C57BL/6NTac-Abcb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492679	M	MP:0005553	increased circulating creatinine level	Abcb4<em1(IMPC)H>/Abcb4<em1(IMPC)H>	C57BL/6NTac-Abcb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492679	F	MP:0005562	decreased mean corpuscular hemoglobin	Abcb4<em1(IMPC)H>/Abcb4<em1(IMPC)H>	C57BL/6NTac-Abcb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492679	F	MP:0005627	increased circulating potassium level	Abcb4<em1(IMPC)H>/Abcb4<em1(IMPC)H>	C57BL/6NTac-Abcb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492682	F	MP:0000702	enlarged lymph nodes	Ablim3<em1(IMPC)Tcp>/Ablim3<em1(IMPC)Tcp>	C57BL/6N-Ablim3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492682	F	MP:0001293	anophthalmia	Ablim3<em1(IMPC)Tcp>/Ablim3<em1(IMPC)Tcp>	C57BL/6N-Ablim3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492682	M	MP:0020421	increased freezing behavior	Ablim3<em1(IMPC)Tcp>/Ablim3<em1(IMPC)Tcp>	C57BL/6N-Ablim3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492682	M	MP:0002608	increased hematocrit	Ablim3<em1(IMPC)Tcp>/Ablim3<em1(IMPC)Tcp>	C57BL/6N-Ablim3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492682	M	MP:0002607	decreased basophil cell number	Ablim3<em1(IMPC)Tcp>/Ablim3<em1(IMPC)Tcp>	C57BL/6N-Ablim3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492683	M	MP:0001146	abnormal testis morphology	Abo<tm1.1(KOMP)Vlcg>/Abo<tm1.1(KOMP)Vlcg>	C57BL/6N-Abo<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6492683	M	MP:0002060	abnormal skin morphology	Abo<tm1.1(KOMP)Vlcg>/Abo<tm1.1(KOMP)Vlcg>	C57BL/6N-Abo<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6492683	M	MP:0001147	small testis	Abo<tm1.1(KOMP)Vlcg>/Abo<tm1.1(KOMP)Vlcg>	C57BL/6N-Abo<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6492684	M	MP:0000274	enlarged heart	Abtb1<em1(IMPC)Ccpcz>/Abtb1<em1(IMPC)Ccpcz>	C57BL/6N-Abtb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492684	M	MP:0000689	abnormal spleen morphology	Abtb1<em1(IMPC)Ccpcz>/Abtb1<em1(IMPC)Ccpcz>	C57BL/6N-Abtb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492684	M	MP:0002060	abnormal skin morphology	Abtb1<em1(IMPC)Ccpcz>/Abtb1<em1(IMPC)Ccpcz>	C57BL/6N-Abtb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492684	M	MP:0013279	increased fasting circulating glucose level	Abtb1<em1(IMPC)Ccpcz>/Abtb1<em1(IMPC)Ccpcz>	C57BL/6N-Abtb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492684	M	MP:0000691	enlarged spleen	Abtb1<em1(IMPC)Ccpcz>/Abtb1<em1(IMPC)Ccpcz>	C57BL/6N-Abtb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492684	M	MP:0000266	abnormal heart morphology	Abtb1<em1(IMPC)Ccpcz>/Abtb1<em1(IMPC)Ccpcz>	C57BL/6N-Abtb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492685	F	MP:0010393	shortened QRS complex duration	Acad11<em1(IMPC)J>/Acad11<em1(IMPC)J>	C57BL/6NJ-Acad11<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492685	F	MP:0010052	increased grip strength	Acad11<em1(IMPC)J>/Acad11<em1(IMPC)J>	C57BL/6NJ-Acad11<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492686	F	MP:0001926	female infertility	Actl6b<em1(IMPC)J>/Actl6b<em1(IMPC)J>	C57BL/6NJ-Actl6b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492687	M	MP:0001925	male infertility	Adam5<em1(IMPC)J>/Adam5<em1(IMPC)J>	C57BL/6NJ-Adam5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492687	M	MP:0002591	decreased mean corpuscular volume	Adam5<em1(IMPC)J>/Adam5<em1(IMPC)J>	C57BL/6NJ-Adam5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492689	F	MP:0001258	decreased body length	Adgrg5<tm1b(EUCOMM)Wtsi>/Adgrg5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Adgrg5<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6492689	F	MP:0008806	increased circulating amylase level	Adgrg5<tm1b(EUCOMM)Wtsi>/Adgrg5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Adgrg5<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6492690	F	MP:0011960	abnormal eye anterior chamber depth	Adgrg7<tm1b(EUCOMM)Hmgu>/Adgrg7<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adgrg7<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6492690	M	MP:0002834	decreased heart weight	Adgrg7<tm1b(EUCOMM)Hmgu>/Adgrg7<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adgrg7<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6492690	M	MP:0011965	decreased total retina thickness	Adgrg7<tm1b(EUCOMM)Hmgu>/Adgrg7<tm1b(EUCOMM)Hmgu>	C57BL/6N-Adgrg7<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6492691	F	MP:0002989	small kidney	Aff4<em1(IMPC)Mbp>/Aff4<+>	C57BL/6N-Aff4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492691	M	MP:0020421	increased freezing behavior	Aff4<em1(IMPC)Mbp>/Aff4<+>	C57BL/6N-Aff4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492691	F	MP:0002135	abnormal kidney morphology	Aff4<em1(IMPC)Mbp>/Aff4<+>	C57BL/6N-Aff4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492691	M	MP:0002060	abnormal skin morphology	Aff4<em1(IMPC)Mbp>/Aff4<+>	C57BL/6N-Aff4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492692	M	MP:0010024	increased total body fat amount	Agbl1<em1(IMPC)J>/Agbl1<em1(IMPC)J>	C57BL/6NJ-Agbl1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492692	F	MP:0001513	limb grasping	Agbl1<em1(IMPC)J>/Agbl1<em1(IMPC)J>	C57BL/6NJ-Agbl1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492692	F	MP:0001284	absent vibrissae	Agbl1<em1(IMPC)J>/Agbl1<em1(IMPC)J>	C57BL/6NJ-Agbl1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492692	M	MP:0003961	decreased lean body mass	Agbl1<em1(IMPC)J>/Agbl1<em1(IMPC)J>	C57BL/6NJ-Agbl1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492696	M	MP:0005013	increased lymphocyte cell number	Amdhd1<tm2b(EUCOMM)Hmgu>/Amdhd1<tm2b(EUCOMM)Hmgu>	C57BL/6N-Amdhd1<tm2b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6492699	M	MP:0001489	decreased startle reflex	Ankrd24<em1(IMPC)J>/Ankrd24<em1(IMPC)J>	C57BL/6NJ-Ankrd24<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492700	M	MP:0010067	increased red blood cell distribution width	Antxr2<em1(IMPC)Wtsi>/Antxr2<em1(IMPC)Wtsi>	C57BL/6N-Antxr2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6492700	F	MP:0002968	increased circulating alkaline phosphatase level	Antxr2<em1(IMPC)Wtsi>/Antxr2<em1(IMPC)Wtsi>	C57BL/6N-Antxr2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6492700	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Antxr2<em1(IMPC)Wtsi>/Antxr2<em1(IMPC)Wtsi>	C57BL/6N-Antxr2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6492701	F	MP:0001402	decreased locomotor activity	Ap5m1<em1(IMPC)Mbp>/Ap5m1<em1(IMPC)Mbp>	C57BL/6N-Ap5m1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492701	F	MP:0002339	abnormal lymph node morphology	Ap5m1<em1(IMPC)Mbp>/Ap5m1<em1(IMPC)Mbp>	C57BL/6N-Ap5m1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492701	F	MP:0005568	increased circulating total protein level	Ap5m1<em1(IMPC)Mbp>/Ap5m1<em1(IMPC)Mbp>	C57BL/6N-Ap5m1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492701	F	MP:0002965	increased circulating serum albumin level	Ap5m1<em1(IMPC)Mbp>/Ap5m1<em1(IMPC)Mbp>	C57BL/6N-Ap5m1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492701	F	MP:0000702	enlarged lymph nodes	Ap5m1<em1(IMPC)Mbp>/Ap5m1<em1(IMPC)Mbp>	C57BL/6N-Ap5m1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492701	M	MP:0002060	abnormal skin morphology	Ap5m1<em1(IMPC)Mbp>/Ap5m1<em1(IMPC)Mbp>	C57BL/6N-Ap5m1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492701	M	MP:0020421	increased freezing behavior	Ap5m1<em1(IMPC)Mbp>/Ap5m1<em1(IMPC)Mbp>	C57BL/6N-Ap5m1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492702	M	MP:0002075	abnormal coat/hair pigmentation	Apex2<em1(IMPC)H>/Y	C57BL/6NTac-Apex2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492703	F	MP:0002875	decreased erythrocyte cell number	Apex2<em1(IMPC)H>/Apex2<em1(IMPC)H>	C57BL/6NTac-Apex2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492703	F	MP:0005016	decreased lymphocyte cell number	Apex2<em1(IMPC)H>/Apex2<em1(IMPC)H>	C57BL/6NTac-Apex2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492703	F	MP:0002590	increased mean corpuscular volume	Apex2<em1(IMPC)H>/Apex2<em1(IMPC)H>	C57BL/6NTac-Apex2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492703	F	MP:0000219	increased neutrophil cell number	Apex2<em1(IMPC)H>/Apex2<em1(IMPC)H>	C57BL/6NTac-Apex2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492703	F	MP:0001402	decreased locomotor activity	Apex2<em1(IMPC)H>/Apex2<em1(IMPC)H>	C57BL/6NTac-Apex2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492703	F	MP:0000443	abnormal snout morphology	Apex2<em1(IMPC)H>/Apex2<em1(IMPC)H>	C57BL/6NTac-Apex2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492707	F	MP:0010123	increased bone mineral content	Arhgef16<em1(IMPC)Mbp>/Arhgef16<em1(IMPC)Mbp>	C57BL/6NCrl-Arhgef16<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492707	M	MP:0003068	enlarged kidney	Arhgef16<em1(IMPC)Mbp>/Arhgef16<em1(IMPC)Mbp>	C57BL/6NCrl-Arhgef16<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492707	M	MP:0000274	enlarged heart	Arhgef16<em1(IMPC)Mbp>/Arhgef16<em1(IMPC)Mbp>	C57BL/6NCrl-Arhgef16<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492707	M	MP:0002135	abnormal kidney morphology	Arhgef16<em1(IMPC)Mbp>/Arhgef16<em1(IMPC)Mbp>	C57BL/6NCrl-Arhgef16<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492707	F	MP:0020421	increased freezing behavior	Arhgef16<em1(IMPC)Mbp>/Arhgef16<em1(IMPC)Mbp>	C57BL/6NCrl-Arhgef16<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492707	M	MP:0000266	abnormal heart morphology	Arhgef16<em1(IMPC)Mbp>/Arhgef16<em1(IMPC)Mbp>	C57BL/6NCrl-Arhgef16<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492709	M	MP:0010506	prolonged RR interval	Arl5a<em1(IMPC)J>/Arl5a<em1(IMPC)J>	C57BL/6NJ-Arl5a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492709	M	MP:0005333	decreased heart rate	Arl5a<em1(IMPC)J>/Arl5a<em1(IMPC)J>	C57BL/6NJ-Arl5a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492711	M	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	M	MP:0001402	decreased locomotor activity	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	M	MP:0000274	enlarged heart	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	M	MP:0001417	decreased exploration in new environment	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	F	MP:0010053	decreased grip strength	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	M	MP:0001293	anophthalmia	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	M	MP:0000221	decreased leukocyte cell number	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	M	MP:0013279	increased fasting circulating glucose level	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	F	MP:0004906	enlarged uterus	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	M	MP:0002060	abnormal skin morphology	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	M	MP:0000266	abnormal heart morphology	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	F	MP:0002968	increased circulating alkaline phosphatase level	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	M	MP:0010574	dilated aorta	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	M	MP:0003917	increased kidney weight	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	F	MP:0001120	abnormal uterus morphology	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492711	M	MP:0005016	decreased lymphocyte cell number	Asb7<em1(IMPC)Ccpcz>/Asb7<em1(IMPC)Ccpcz>	C57BL/6N-Asb7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492714	M	MP:0000274	enlarged heart	Atg7<em1(IMPC)Ccpcz>/Atg7<+>	C57BL/6N-Atg7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492714	M	MP:0000266	abnormal heart morphology	Atg7<em1(IMPC)Ccpcz>/Atg7<+>	C57BL/6N-Atg7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492714	F	MP:0001325	abnormal retina morphology	Atg7<em1(IMPC)Ccpcz>/Atg7<+>	C57BL/6N-Atg7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492714	M	MP:0002060	abnormal skin morphology	Atg7<em1(IMPC)Ccpcz>/Atg7<+>	C57BL/6N-Atg7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492716	M	MP:0001289	persistence of hyaloid vascular system	Atp11b<em1(IMPC)Tcp>/Atp11b<em1(IMPC)Tcp>	C57BL/6N-Atp11b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492716	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Atp11b<em1(IMPC)Tcp>/Atp11b<em1(IMPC)Tcp>	C57BL/6N-Atp11b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492716	F	MP:0005562	decreased mean corpuscular hemoglobin	Atp11b<em1(IMPC)Tcp>/Atp11b<em1(IMPC)Tcp>	C57BL/6N-Atp11b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492716	F	MP:0004832	enlarged ovary	Atp11b<em1(IMPC)Tcp>/Atp11b<em1(IMPC)Tcp>	C57BL/6N-Atp11b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492717	F	MP:0003717	pallor	Atp13a1<em1(IMPC)Tcp>/Atp13a1<em1(IMPC)Tcp>	C57BL/6N-Atp13a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492718	M	MP:0002092	abnormal eye morphology	Awat2<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Awat2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492718	M	MP:0000538	abnormal urinary bladder morphology	Awat2<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Awat2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492718	M	MP:0002339	abnormal lymph node morphology	Awat2<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Awat2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492718	M	MP:0001340	abnormal eyelid morphology	Awat2<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Awat2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492718	M	MP:0006203	eye hemorrhage	Awat2<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Awat2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492719	F	MP:0001566	increased circulating phosphate level	Bag2<em1(IMPC)J>/Bag2<em1(IMPC)J>	C57BL/6NJ-Bag2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492719	F	MP:0013279	increased fasting circulating glucose level	Bag2<em1(IMPC)J>/Bag2<em1(IMPC)J>	C57BL/6NJ-Bag2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492721	F	MP:0010090	increased circulating creatine kinase level	Birc6<em1(IMPC)Ccpcz>/Birc6<+>	C57BL/6N-Birc6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492721	M	MP:0000274	enlarged heart	Birc6<em1(IMPC)Ccpcz>/Birc6<+>	C57BL/6N-Birc6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492721	M	MP:0000266	abnormal heart morphology	Birc6<em1(IMPC)Ccpcz>/Birc6<+>	C57BL/6N-Birc6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492721	F	MP:0001325	abnormal retina morphology	Birc6<em1(IMPC)Ccpcz>/Birc6<+>	C57BL/6N-Birc6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492723	M	MP:0002059	abnormal seminal vesicle morphology	Bnc1<em1(IMPC)H>/Bnc1<em1(IMPC)H>	C57BL/6NTac-Bnc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492723	F	MP:0002075	abnormal coat/hair pigmentation	Bnc1<em1(IMPC)H>/Bnc1<em1(IMPC)H>	C57BL/6NTac-Bnc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492723	M	MP:0001147	small testis	Bnc1<em1(IMPC)H>/Bnc1<em1(IMPC)H>	C57BL/6NTac-Bnc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492723	M	MP:0005013	increased lymphocyte cell number	Bnc1<em1(IMPC)H>/Bnc1<em1(IMPC)H>	C57BL/6NTac-Bnc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492723	F	MP:0000367	abnormal coat/ hair morphology	Bnc1<em1(IMPC)H>/Bnc1<em1(IMPC)H>	C57BL/6NTac-Bnc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492723	M	MP:0010123	increased bone mineral content	Bnc1<em1(IMPC)H>/Bnc1<em1(IMPC)H>	C57BL/6NTac-Bnc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492723	F	MP:0001926	female infertility	Bnc1<em1(IMPC)H>/Bnc1<em1(IMPC)H>	C57BL/6NTac-Bnc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492723	M	MP:0002941	increased circulating alanine transaminase level	Bnc1<em1(IMPC)H>/Bnc1<em1(IMPC)H>	C57BL/6NTac-Bnc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492723	F	MP:0000219	increased neutrophil cell number	Bnc1<em1(IMPC)H>/Bnc1<em1(IMPC)H>	C57BL/6NTac-Bnc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492724	M	MP:0000692	small spleen	Bnip5<tm1.1(KOMP)Vlcg>/Bnip5<tm1.1(KOMP)Vlcg>	C57BL/6N-Bnip5<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6492724	M	MP:0000689	abnormal spleen morphology	Bnip5<tm1.1(KOMP)Vlcg>/Bnip5<tm1.1(KOMP)Vlcg>	C57BL/6N-Bnip5<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6492724	F	MP:0002941	increased circulating alanine transaminase level	Bnip5<tm1.1(KOMP)Vlcg>/Bnip5<tm1.1(KOMP)Vlcg>	C57BL/6N-Bnip5<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6492725	M	MP:0005293	impaired glucose tolerance	Bpifc<em1(IMPC)J>/Bpifc<em1(IMPC)J>	C57BL/6NJ-Bpifc<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492725	F	MP:0005655	increased aggression	Bpifc<em1(IMPC)J>/Bpifc<em1(IMPC)J>	C57BL/6NJ-Bpifc<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492726	F	MP:0001392	abnormal locomotor behavior	Brme1<em1(IMPC)J>/Brme1<em1(IMPC)J>	C57BL/6NJ-Brme1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492727	F	MP:0002941	increased circulating alanine transaminase level	Bysl<em1(IMPC)Ccpcz>/Bysl<+>	C57BL/6N-Bysl<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492727	F	MP:0002060	abnormal skin morphology	Bysl<em1(IMPC)Ccpcz>/Bysl<+>	C57BL/6N-Bysl<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492727	M	MP:0000274	enlarged heart	Bysl<em1(IMPC)Ccpcz>/Bysl<+>	C57BL/6N-Bysl<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492727	M	MP:0000266	abnormal heart morphology	Bysl<em1(IMPC)Ccpcz>/Bysl<+>	C57BL/6N-Bysl<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492729	M	MP:0001417	decreased exploration in new environment	C2cd2l<em1(IMPC)J>/C2cd2l<em1(IMPC)J>	C57BL/6NJ-C2cd2l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492730	F	MP:0000601	small liver	Cacna1c<em1(IMPC)Mbp>/Cacna1c<+>	C57BL/6N-Cacna1c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492730	F	MP:0002135	abnormal kidney morphology	Cacna1c<em1(IMPC)Mbp>/Cacna1c<+>	C57BL/6N-Cacna1c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492730	F	MP:0000691	enlarged spleen	Cacna1c<em1(IMPC)Mbp>/Cacna1c<+>	C57BL/6N-Cacna1c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492730	F	MP:0000689	abnormal spleen morphology	Cacna1c<em1(IMPC)Mbp>/Cacna1c<+>	C57BL/6N-Cacna1c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492730	F	MP:0002989	small kidney	Cacna1c<em1(IMPC)Mbp>/Cacna1c<+>	C57BL/6N-Cacna1c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492730	F	MP:0000598	abnormal liver morphology	Cacna1c<em1(IMPC)Mbp>/Cacna1c<+>	C57BL/6N-Cacna1c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492730	M	MP:0020421	increased freezing behavior	Cacna1c<em1(IMPC)Mbp>/Cacna1c<+>	C57BL/6N-Cacna1c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492731	M	MP:0001392	abnormal locomotor behavior	Cacng5<em1(IMPC)H>/Cacng5<em1(IMPC)H>	C57BL/6NTac-Cacng5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492734	F	MP:0009709	hydrometra	Camkv<em1(IMPC)Mbp>/Camkv<em1(IMPC)Mbp>	C57BL/6NCrl-Camkv<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492734	M	MP:0009476	enlarged cecum	Camkv<em1(IMPC)Mbp>/Camkv<em1(IMPC)Mbp>	C57BL/6NCrl-Camkv<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492734	F	MP:0001120	abnormal uterus morphology	Camkv<em1(IMPC)Mbp>/Camkv<em1(IMPC)Mbp>	C57BL/6NCrl-Camkv<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492734	M	MP:0000494	abnormal cecum morphology	Camkv<em1(IMPC)Mbp>/Camkv<em1(IMPC)Mbp>	C57BL/6NCrl-Camkv<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492735	F	MP:0000702	enlarged lymph nodes	Carmil3<em1(IMPC)Mbp>/Carmil3<em1(IMPC)Mbp>	C57BL/6N-Carmil3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492735	F	MP:0002135	abnormal kidney morphology	Carmil3<em1(IMPC)Mbp>/Carmil3<em1(IMPC)Mbp>	C57BL/6N-Carmil3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492735	F	MP:0001417	decreased exploration in new environment	Carmil3<em1(IMPC)Mbp>/Carmil3<em1(IMPC)Mbp>	C57BL/6N-Carmil3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492735	F	MP:0002060	abnormal skin morphology	Carmil3<em1(IMPC)Mbp>/Carmil3<em1(IMPC)Mbp>	C57BL/6N-Carmil3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492735	F	MP:0002339	abnormal lymph node morphology	Carmil3<em1(IMPC)Mbp>/Carmil3<em1(IMPC)Mbp>	C57BL/6N-Carmil3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492736	M	MP:0002631	abnormal epididymis morphology	Casc3<tm1.1(KOMP)Vlcg>/Casc3<+>	C57BL/6N-Casc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6492736	M	MP:0000266	abnormal heart morphology	Casc3<tm1.1(KOMP)Vlcg>/Casc3<+>	C57BL/6N-Casc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6492736	M	MP:0000274	enlarged heart	Casc3<tm1.1(KOMP)Vlcg>/Casc3<+>	C57BL/6N-Casc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6492736	M	MP:0004931	enlarged epididymis	Casc3<tm1.1(KOMP)Vlcg>/Casc3<+>	C57BL/6N-Casc3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6492737	F	MP:0000703	abnormal thymus morphology	Casp14<em1(IMPC)Ccpcz>/Casp14<em1(IMPC)Ccpcz>	C57BL/6N-Casp14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492737	F	MP:0000709	enlarged thymus	Casp14<em1(IMPC)Ccpcz>/Casp14<em1(IMPC)Ccpcz>	C57BL/6N-Casp14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492737	M	MP:0000689	abnormal spleen morphology	Casp14<em1(IMPC)Ccpcz>/Casp14<em1(IMPC)Ccpcz>	C57BL/6N-Casp14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492737	F	MP:0002060	abnormal skin morphology	Casp14<em1(IMPC)Ccpcz>/Casp14<em1(IMPC)Ccpcz>	C57BL/6N-Casp14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492737	F	MP:0011239	abnormal skin coloration	Casp14<em1(IMPC)Ccpcz>/Casp14<em1(IMPC)Ccpcz>	C57BL/6N-Casp14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492740	F	MP:0002968	increased circulating alkaline phosphatase level	Ccdc117<em1(IMPC)J>/Ccdc117<em1(IMPC)J>	C57BL/6NJ-Ccdc117<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492742	M	MP:0005543	decreased cornea thickness	Ccdc180<tm1b(KOMP)Wtsi>/Ccdc180<+>	C57BL/6N-Ccdc180<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6492743	M	MP:0005561	increased mean corpuscular hemoglobin	Ccdc51<em1(IMPC)J>/Ccdc51<em1(IMPC)J>	C57BL/6NJ-Ccdc51<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492743	F	MP:0013279	increased fasting circulating glucose level	Ccdc51<em1(IMPC)J>/Ccdc51<em1(IMPC)J>	C57BL/6NJ-Ccdc51<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492745	F	MP:0000691	enlarged spleen	Ccl25<em1(IMPC)H>/Ccl25<em1(IMPC)H>	C57BL/6N-Ccl25<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492745	F	MP:0013278	decreased fasting circulating glucose level	Ccl25<em1(IMPC)H>/Ccl25<em1(IMPC)H>	C57BL/6N-Ccl25<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492745	F	MP:0004952	increased spleen weight	Ccl25<em1(IMPC)H>/Ccl25<em1(IMPC)H>	C57BL/6N-Ccl25<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492746	M	MP:0005561	increased mean corpuscular hemoglobin	Ccnt1<em1(IMPC)J>/Ccnt1<em1(IMPC)J>	C57BL/6NJ-Ccnt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492746	M	MP:0002875	decreased erythrocyte cell number	Ccnt1<em1(IMPC)J>/Ccnt1<em1(IMPC)J>	C57BL/6NJ-Ccnt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492746	F	MP:0000218	increased leukocyte cell number	Ccnt1<em1(IMPC)J>/Ccnt1<em1(IMPC)J>	C57BL/6NJ-Ccnt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492746	F	MP:0001417	decreased exploration in new environment	Ccnt1<em1(IMPC)J>/Ccnt1<em1(IMPC)J>	C57BL/6NJ-Ccnt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492746	F	MP:0002968	increased circulating alkaline phosphatase level	Ccnt1<em1(IMPC)J>/Ccnt1<em1(IMPC)J>	C57BL/6NJ-Ccnt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492746	M	MP:0002590	increased mean corpuscular volume	Ccnt1<em1(IMPC)J>/Ccnt1<em1(IMPC)J>	C57BL/6NJ-Ccnt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492747	F	MP:0005011	increased eosinophil cell number	Ccr2<em1(IMPC)H>/Ccr2<em1(IMPC)H>	C57BL/6N-Ccr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492747	F	MP:0005599	increased cardiac muscle contractility	Ccr2<em1(IMPC)H>/Ccr2<em1(IMPC)H>	C57BL/6N-Ccr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492747	M	MP:0000222	decreased neutrophil cell number	Ccr2<em1(IMPC)H>/Ccr2<em1(IMPC)H>	C57BL/6N-Ccr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492747	F	MP:0001406	abnormal gait	Ccr2<em1(IMPC)H>/Ccr2<em1(IMPC)H>	C57BL/6N-Ccr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492747	F	MP:0005016	decreased lymphocyte cell number	Ccr2<em1(IMPC)H>/Ccr2<em1(IMPC)H>	C57BL/6N-Ccr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492747	M	MP:0000274	enlarged heart	Ccr2<em1(IMPC)H>/Ccr2<em1(IMPC)H>	C57BL/6N-Ccr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492747	F	MP:0003921	abnormal heart left ventricle morphology	Ccr2<em1(IMPC)H>/Ccr2<em1(IMPC)H>	C57BL/6N-Ccr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492750	F	MP:0000220	increased monocyte cell number	Cd74<em1(IMPC)H>/Cd74<em1(IMPC)H>	C57BL/6N-Cd74<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492754	M	MP:0000367	abnormal coat/ hair morphology	Cdh12<em1(IMPC)J>/Cdh12<em1(IMPC)J>	C57BL/6NJ-Cdh12<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492756	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Cdsn<tm1b(EUCOMM)Hmgu>/Cdsn<+>	C57BL/6N-Cdsn<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6492756	F	MP:0005561	increased mean corpuscular hemoglobin	Cdsn<tm1b(EUCOMM)Hmgu>/Cdsn<+>	C57BL/6N-Cdsn<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6492757	F	MP:0001926	female infertility	Celsr1<em1(IMPC)Mbp>/Celsr1<em1(IMPC)Mbp>	C57BL/6N-Celsr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492757	M	MP:0001925	male infertility	Celsr1<em1(IMPC)Mbp>/Celsr1<em1(IMPC)Mbp>	C57BL/6N-Celsr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492759	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Cep290<em1(IMPC)Mbp>/Cep290<+>	C57BL/6N-Cep290<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492760	M	MP:0001925	male infertility	Cep78<em1(IMPC)J>/Cep78<em1(IMPC)J>	C57BL/6NJ-Cep78<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492761	M	MP:0000702	enlarged lymph nodes	Cep85l<em1(IMPC)Mbp>/Cep85l<em1(IMPC)Mbp>	C57BL/6N-Cep85l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492761	M	MP:0001489	decreased startle reflex	Cep85l<em1(IMPC)Mbp>/Cep85l<em1(IMPC)Mbp>	C57BL/6N-Cep85l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492761	M	MP:0001486	abnormal startle reflex	Cep85l<em1(IMPC)Mbp>/Cep85l<em1(IMPC)Mbp>	C57BL/6N-Cep85l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492761	M	MP:0002135	abnormal kidney morphology	Cep85l<em1(IMPC)Mbp>/Cep85l<em1(IMPC)Mbp>	C57BL/6N-Cep85l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492761	M	MP:0002339	abnormal lymph node morphology	Cep85l<em1(IMPC)Mbp>/Cep85l<em1(IMPC)Mbp>	C57BL/6N-Cep85l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492761	M	MP:0003068	enlarged kidney	Cep85l<em1(IMPC)Mbp>/Cep85l<em1(IMPC)Mbp>	C57BL/6N-Cep85l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492761	F	MP:0002060	abnormal skin morphology	Cep85l<em1(IMPC)Mbp>/Cep85l<em1(IMPC)Mbp>	C57BL/6N-Cep85l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492765	M	MP:0000691	enlarged spleen	Ciao2b<em1(IMPC)Ccpcz>/Ciao2b<+>	C57BL/6N-Ciao2b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492765	M	MP:0000274	enlarged heart	Ciao2b<em1(IMPC)Ccpcz>/Ciao2b<+>	C57BL/6N-Ciao2b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492765	M	MP:0002060	abnormal skin morphology	Ciao2b<em1(IMPC)Ccpcz>/Ciao2b<+>	C57BL/6N-Ciao2b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492765	M	MP:0000266	abnormal heart morphology	Ciao2b<em1(IMPC)Ccpcz>/Ciao2b<+>	C57BL/6N-Ciao2b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492765	M	MP:0000219	increased neutrophil cell number	Ciao2b<em1(IMPC)Ccpcz>/Ciao2b<+>	C57BL/6N-Ciao2b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492767	M	MP:0000274	enlarged heart	Cilk1<tm1b(KOMP)Mbp>/Cilk1<tm1b(KOMP)Mbp>	C57BL/6N-Cilk1<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6492767	M	MP:0000219	increased neutrophil cell number	Cilk1<tm1b(KOMP)Mbp>/Cilk1<tm1b(KOMP)Mbp>	C57BL/6N-Cilk1<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6492767	M	MP:0000266	abnormal heart morphology	Cilk1<tm1b(KOMP)Mbp>/Cilk1<tm1b(KOMP)Mbp>	C57BL/6N-Cilk1<tm1b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:6492771	M	MP:0003960	increased lean body mass	Clec3a<em1(IMPC)J>/Clec3a<em1(IMPC)J>	C57BL/6NJ-Clec3a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492771	F	MP:0001399	hyperactivity	Clec3a<em1(IMPC)J>/Clec3a<em1(IMPC)J>	C57BL/6NJ-Clec3a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492771	M	MP:0010025	decreased total body fat amount	Clec3a<em1(IMPC)J>/Clec3a<em1(IMPC)J>	C57BL/6NJ-Clec3a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492771	M	MP:0000062	increased bone mineral density	Clec3a<em1(IMPC)J>/Clec3a<em1(IMPC)J>	C57BL/6NJ-Clec3a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492771	F	MP:0001284	absent vibrissae	Clec3a<em1(IMPC)J>/Clec3a<em1(IMPC)J>	C57BL/6NJ-Clec3a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492778	M	MP:0002941	increased circulating alanine transaminase level	Cpsf4l<em1(IMPC)J>/Cpsf4l<em1(IMPC)J>	C57BL/6NJ-Cpsf4l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492779	F	MP:0002060	abnormal skin morphology	Cpxm1<em1(IMPC)Tcp>/Cpxm1<em1(IMPC)Tcp>	C57BL/6N-Cpxm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492779	F	MP:0000220	increased monocyte cell number	Cpxm1<em1(IMPC)Tcp>/Cpxm1<em1(IMPC)Tcp>	C57BL/6N-Cpxm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492779	F	MP:0001293	anophthalmia	Cpxm1<em1(IMPC)Tcp>/Cpxm1<em1(IMPC)Tcp>	C57BL/6N-Cpxm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492779	M	MP:0000702	enlarged lymph nodes	Cpxm1<em1(IMPC)Tcp>/Cpxm1<em1(IMPC)Tcp>	C57BL/6N-Cpxm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492780	F	MP:0010053	decreased grip strength	Creg2<em1(IMPC)J>/Creg2<em1(IMPC)J>	C57BL/6NJ-Creg2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492780	F	MP:0013278	decreased fasting circulating glucose level	Creg2<em1(IMPC)J>/Creg2<em1(IMPC)J>	C57BL/6NJ-Creg2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492780	M	MP:0000367	abnormal coat/ hair morphology	Creg2<em1(IMPC)J>/Creg2<em1(IMPC)J>	C57BL/6NJ-Creg2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492781	M	MP:0001147	small testis	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492781	F	MP:0008044	increased NK cell number	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492781	M	MP:0011874	enlarged urinary bladder	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492781	F	MP:0000709	enlarged thymus	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492781	M	MP:0000538	abnormal urinary bladder morphology	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492781	M	MP:0000274	enlarged heart	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492781	F	MP:0001417	decreased exploration in new environment	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492781	M	MP:0002059	abnormal seminal vesicle morphology	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492781	M	MP:0000706	small thymus	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492781	M	MP:0000266	abnormal heart morphology	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492781	F	MP:0002764	short tibia	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492781	F	MP:0002060	abnormal skin morphology	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492781	M	MP:0001146	abnormal testis morphology	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492781	M	MP:0013279	increased fasting circulating glucose level	Crx<em1(IMPC)Ccpcz>/Crx<em1(IMPC)Ccpcz>	C57BL/6N-Crx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492782	F	MP:0002792	abnormal retina vasculature morphology	Cstdc3<em1(IMPC)Tcp>/Cstdc3<em1(IMPC)Tcp>	C57BL/6N-Cstdc3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492782	F	MP:0010097	abnormal retina blood vessel morphology	Cstdc3<em1(IMPC)Tcp>/Cstdc3<em1(IMPC)Tcp>	C57BL/6N-Cstdc3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492784	M	MP:0000702	enlarged lymph nodes	Ctps1<em1(IMPC)Tcp>/Ctps1<+>	C57BL/6N-Ctps1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492784	M	MP:0002060	abnormal skin morphology	Ctps1<em1(IMPC)Tcp>/Ctps1<+>	C57BL/6N-Ctps1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492784	M	MP:0011874	enlarged urinary bladder	Ctps1<em1(IMPC)Tcp>/Ctps1<+>	C57BL/6N-Ctps1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492786	M	MP:0005627	increased circulating potassium level	Cul9<em1(IMPC)Ccpcz>/Cul9<em1(IMPC)Ccpcz>	C57BL/6N-Cul9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492786	M	MP:0005565	increased blood urea nitrogen level	Cul9<em1(IMPC)Ccpcz>/Cul9<em1(IMPC)Ccpcz>	C57BL/6N-Cul9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492786	M	MP:0011971	increased circulating lactate dehydrogenase level	Cul9<em1(IMPC)Ccpcz>/Cul9<em1(IMPC)Ccpcz>	C57BL/6N-Cul9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492786	F	MP:0000703	abnormal thymus morphology	Cul9<em1(IMPC)Ccpcz>/Cul9<em1(IMPC)Ccpcz>	C57BL/6N-Cul9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492786	F	MP:0000709	enlarged thymus	Cul9<em1(IMPC)Ccpcz>/Cul9<em1(IMPC)Ccpcz>	C57BL/6N-Cul9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492786	M	MP:0010090	increased circulating creatine kinase level	Cul9<em1(IMPC)Ccpcz>/Cul9<em1(IMPC)Ccpcz>	C57BL/6N-Cul9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492786	F	MP:0000137	abnormal vertebrae morphology	Cul9<em1(IMPC)Ccpcz>/Cul9<em1(IMPC)Ccpcz>	C57BL/6N-Cul9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492786	F	MP:0000689	abnormal spleen morphology	Cul9<em1(IMPC)Ccpcz>/Cul9<em1(IMPC)Ccpcz>	C57BL/6N-Cul9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492786	F	MP:0002135	abnormal kidney morphology	Cul9<em1(IMPC)Ccpcz>/Cul9<em1(IMPC)Ccpcz>	C57BL/6N-Cul9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492786	F	MP:0000691	enlarged spleen	Cul9<em1(IMPC)Ccpcz>/Cul9<em1(IMPC)Ccpcz>	C57BL/6N-Cul9<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492787	F	MP:0002092	abnormal eye morphology	Cuta<em1(IMPC)Mbp>/Cuta<em1(IMPC)Mbp>	C57BL/6N-Cuta<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492787	M	MP:0000598	abnormal liver morphology	Cuta<em1(IMPC)Mbp>/Cuta<em1(IMPC)Mbp>	C57BL/6N-Cuta<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492787	M	MP:0002135	abnormal kidney morphology	Cuta<em1(IMPC)Mbp>/Cuta<em1(IMPC)Mbp>	C57BL/6N-Cuta<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492787	F	MP:0001297	microphthalmia	Cuta<em1(IMPC)Mbp>/Cuta<em1(IMPC)Mbp>	C57BL/6N-Cuta<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492787	M	MP:0003068	enlarged kidney	Cuta<em1(IMPC)Mbp>/Cuta<em1(IMPC)Mbp>	C57BL/6N-Cuta<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492788	M	MP:0001392	abnormal locomotor behavior	Cwh43<em1(IMPC)J>/Cwh43<em1(IMPC)J>	C57BL/6NJ-Cwh43<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492789	M	MP:0003068	enlarged kidney	Cx3cr1<em1(IMPC)Mbp>/Cx3cr1<em1(IMPC)Mbp>	C57BL/6N-Cx3cr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492789	F	MP:0002989	small kidney	Cx3cr1<em1(IMPC)Mbp>/Cx3cr1<em1(IMPC)Mbp>	C57BL/6N-Cx3cr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492792	M	MP:0011965	decreased total retina thickness	Cyp4f16<tm1b(EUCOMM)Hmgu>/Cyp4f16<tm1b(EUCOMM)Hmgu>	C57BL/6N-Cyp4f16<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6492794	M	MP:0001697	abnormal embryo size	Ddx31<em1(IMPC)J>/Ddx31<em1(IMPC)J>	C57BL/6NJ-Ddx31<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492796	M	MP:0002574	increased vertical activity	Dennd6a<em1(IMPC)J>/Dennd6a<em1(IMPC)J>	C57BL/6NJ-Dennd6a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492798	F	MP:0005554	decreased circulating creatinine level	Dgkh<em1(IMPC)J>/Dgkh<em1(IMPC)J>	C57BL/6NJ-Dgkh<em1(IMPC)J>/J	N	MGI:5576271
MGI:6492799	M	MP:0001488	increased startle reflex	Dhtkd1<em1(IMPC)J>/Dhtkd1<em1(IMPC)J>	C57BL/6NJ-Dhtkd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492801	F	MP:0001297	microphthalmia	Dhx8<em1(IMPC)Mbp>/Dhx8<+>	C57BL/6N-Dhx8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492801	F	MP:0002092	abnormal eye morphology	Dhx8<em1(IMPC)Mbp>/Dhx8<+>	C57BL/6N-Dhx8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492801	F	MP:0000709	enlarged thymus	Dhx8<em1(IMPC)Mbp>/Dhx8<+>	C57BL/6N-Dhx8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492801	F	MP:0000703	abnormal thymus morphology	Dhx8<em1(IMPC)Mbp>/Dhx8<+>	C57BL/6N-Dhx8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492801	M	MP:0003068	enlarged kidney	Dhx8<em1(IMPC)Mbp>/Dhx8<+>	C57BL/6N-Dhx8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492801	F	MP:0002989	small kidney	Dhx8<em1(IMPC)Mbp>/Dhx8<+>	C57BL/6N-Dhx8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492804	M	MP:0005344	increased circulating bilirubin level	Dnajc13<em1(IMPC)J>/Dnajc13<+>	C57BL/6NJ-Dnajc13<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492810	F	MP:0001293	anophthalmia	Dzip1l<em1(IMPC)J>/Dzip1l<em1(IMPC)J>	C57BL/6NJ-Dzip1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492810	F	MP:0001914	hemorrhage	Dzip1l<em1(IMPC)J>/Dzip1l<em1(IMPC)J>	C57BL/6NJ-Dzip1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492811	M	MP:0010506	prolonged RR interval	Efhb<em1(IMPC)J>/Efhb<em1(IMPC)J>	C57BL/6NJ-Efhb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492811	M	MP:0005178	increased circulating cholesterol level	Efhb<em1(IMPC)J>/Efhb<em1(IMPC)J>	C57BL/6NJ-Efhb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492813	F	MP:0001700	abnormal embryo turning	Ehbp1<em1(IMPC)J>/Ehbp1<em1(IMPC)J>	C57BL/6NJ-Ehbp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492814	F	MP:0003961	decreased lean body mass	Eif1ad<tm1b(EUCOMM)Hmgu>/Eif1ad<+>	C57BL/6N-Eif1ad<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6492814	M	MP:0012362	increased large unstained cell number	Eif1ad<tm1b(EUCOMM)Hmgu>/Eif1ad<+>	C57BL/6N-Eif1ad<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6492816	M	MP:0001392	abnormal locomotor behavior	Eif4b<em1(IMPC)J>/Eif4b<+>	C57BL/6NJ-Eif4b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492816	M	MP:0010052	increased grip strength	Eif4b<em1(IMPC)J>/Eif4b<+>	C57BL/6NJ-Eif4b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492818	F	MP:0010053	decreased grip strength	Eif5b<em1(IMPC)J>/Eif5b<+>	C57BL/6NJ-Eif5b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492820	F	MP:0000598	abnormal liver morphology	Eloa<em1(IMPC)Mbp>/Eloa<+>	C57BL/6N-Eloa<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492820	F	MP:0001258	decreased body length	Eloa<em1(IMPC)Mbp>/Eloa<+>	C57BL/6N-Eloa<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492820	F	MP:0001293	anophthalmia	Eloa<em1(IMPC)Mbp>/Eloa<+>	C57BL/6N-Eloa<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492820	F	MP:0002092	abnormal eye morphology	Eloa<em1(IMPC)Mbp>/Eloa<+>	C57BL/6N-Eloa<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492820	F	MP:0000601	small liver	Eloa<em1(IMPC)Mbp>/Eloa<+>	C57BL/6N-Eloa<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492821	F	MP:0002135	abnormal kidney morphology	Eng<em1(IMPC)Mbp>/Eng<+>	C57BL/6N-Eng<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492821	M	MP:0000219	increased neutrophil cell number	Eng<em1(IMPC)Mbp>/Eng<+>	C57BL/6N-Eng<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492821	F	MP:0002989	small kidney	Eng<em1(IMPC)Mbp>/Eng<+>	C57BL/6N-Eng<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492823	M	MP:0010024	increased total body fat amount	Epas1<em1(IMPC)Wtsi>/Epas1<em1(IMPC)Wtsi>	C57BL/6N-Epas1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6492824	F	MP:0002606	increased basophil cell number	Epg5<em1(IMPC)H>/Epg5<em1(IMPC)H>	C57BL/6NTac-Epg5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492824	F	MP:0002626	increased heart rate	Epg5<em1(IMPC)H>/Epg5<em1(IMPC)H>	C57BL/6NTac-Epg5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492824	M	MP:0001489	decreased startle reflex	Epg5<em1(IMPC)H>/Epg5<em1(IMPC)H>	C57BL/6NTac-Epg5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492824	F	MP:0002764	short tibia	Epg5<em1(IMPC)H>/Epg5<em1(IMPC)H>	C57BL/6NTac-Epg5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492824	M	MP:0000062	increased bone mineral density	Epg5<em1(IMPC)H>/Epg5<em1(IMPC)H>	C57BL/6NTac-Epg5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492824	M	MP:0001406	abnormal gait	Epg5<em1(IMPC)H>/Epg5<em1(IMPC)H>	C57BL/6NTac-Epg5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492824	F	MP:0012362	increased large unstained cell number	Epg5<em1(IMPC)H>/Epg5<em1(IMPC)H>	C57BL/6NTac-Epg5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492824	F	MP:0008806	increased circulating amylase level	Epg5<em1(IMPC)H>/Epg5<em1(IMPC)H>	C57BL/6NTac-Epg5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492824	F	MP:0008810	increased circulating iron level	Epg5<em1(IMPC)H>/Epg5<em1(IMPC)H>	C57BL/6NTac-Epg5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492824	F	MP:0005419	decreased circulating serum albumin level	Epg5<em1(IMPC)H>/Epg5<em1(IMPC)H>	C57BL/6NTac-Epg5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492825	F	MP:0001293	anophthalmia	Ercc4<em1(IMPC)J>/Ercc4<em1(IMPC)J>	C57BL/6NJ-Ercc4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492827	M	MP:0010053	decreased grip strength	Ergic1<em1(IMPC)J>/Ergic1<+>	C57BL/6NJ-Ergic1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492830	M	MP:0002965	increased circulating serum albumin level	Exoc3l2<em1(IMPC)J>/Exoc3l2<+>	C57BL/6N-Exoc3l2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6492830	F	MP:0010053	decreased grip strength	Exoc3l2<em1(IMPC)J>/Exoc3l2<+>	C57BL/6N-Exoc3l2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6492830	M	MP:0005293	impaired glucose tolerance	Exoc3l2<em1(IMPC)J>/Exoc3l2<+>	C57BL/6N-Exoc3l2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6492830	M	MP:0002834	decreased heart weight	Exoc3l2<em1(IMPC)J>/Exoc3l2<+>	C57BL/6N-Exoc3l2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6492833	F	MP:0000367	abnormal coat/ hair morphology	Exosc1<em1(IMPC)J>/Exosc1<+>	C57BL/6NJ-Exosc1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492835	F	MP:0000702	enlarged lymph nodes	Eya2<em1(IMPC)Mbp>/Eya2<em1(IMPC)Mbp>	C57BL/6N-Eya2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492835	M	MP:0000689	abnormal spleen morphology	Eya2<em1(IMPC)Mbp>/Eya2<em1(IMPC)Mbp>	C57BL/6N-Eya2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492835	M	MP:0000691	enlarged spleen	Eya2<em1(IMPC)Mbp>/Eya2<em1(IMPC)Mbp>	C57BL/6N-Eya2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492835	F	MP:0000692	small spleen	Eya2<em1(IMPC)Mbp>/Eya2<em1(IMPC)Mbp>	C57BL/6N-Eya2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492835	F	MP:0002339	abnormal lymph node morphology	Eya2<em1(IMPC)Mbp>/Eya2<em1(IMPC)Mbp>	C57BL/6N-Eya2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492837	M	MP:0002060	abnormal skin morphology	Fam124a<em1(IMPC)Ccpcz>/Fam124a<em1(IMPC)Ccpcz>	C57BL/6N-Fam124a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492837	M	MP:0000709	enlarged thymus	Fam124a<em1(IMPC)Ccpcz>/Fam124a<em1(IMPC)Ccpcz>	C57BL/6N-Fam124a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492837	M	MP:0000703	abnormal thymus morphology	Fam124a<em1(IMPC)Ccpcz>/Fam124a<em1(IMPC)Ccpcz>	C57BL/6N-Fam124a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492837	M	MP:0000274	enlarged heart	Fam124a<em1(IMPC)Ccpcz>/Fam124a<em1(IMPC)Ccpcz>	C57BL/6N-Fam124a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492837	M	MP:0000266	abnormal heart morphology	Fam124a<em1(IMPC)Ccpcz>/Fam124a<em1(IMPC)Ccpcz>	C57BL/6N-Fam124a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492838	F	MP:0008259	abnormal optic disk morphology	Fhip2a<em1(IMPC)J>/Fhip2a<em1(IMPC)J>	C57BL/6NJ-Fhip2a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492838	M	MP:0005293	impaired glucose tolerance	Fhip2a<em1(IMPC)J>/Fhip2a<em1(IMPC)J>	C57BL/6NJ-Fhip2a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492838	M	MP:0001392	abnormal locomotor behavior	Fhip2a<em1(IMPC)J>/Fhip2a<em1(IMPC)J>	C57BL/6NJ-Fhip2a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492838	M	MP:0002968	increased circulating alkaline phosphatase level	Fhip2a<em1(IMPC)J>/Fhip2a<em1(IMPC)J>	C57BL/6NJ-Fhip2a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492838	M	MP:0001289	persistence of hyaloid vascular system	Fhip2a<em1(IMPC)J>/Fhip2a<em1(IMPC)J>	C57BL/6NJ-Fhip2a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492839	F	MP:0000689	abnormal spleen morphology	Fhip2b<em1(IMPC)Ccpcz>/Fhip2b<em1(IMPC)Ccpcz>	C57BL/6N-Fhip2b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492839	M	MP:0000274	enlarged heart	Fhip2b<em1(IMPC)Ccpcz>/Fhip2b<em1(IMPC)Ccpcz>	C57BL/6N-Fhip2b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492839	F	MP:0000703	abnormal thymus morphology	Fhip2b<em1(IMPC)Ccpcz>/Fhip2b<em1(IMPC)Ccpcz>	C57BL/6N-Fhip2b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492839	F	MP:0000709	enlarged thymus	Fhip2b<em1(IMPC)Ccpcz>/Fhip2b<em1(IMPC)Ccpcz>	C57BL/6N-Fhip2b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492839	F	MP:0000691	enlarged spleen	Fhip2b<em1(IMPC)Ccpcz>/Fhip2b<em1(IMPC)Ccpcz>	C57BL/6N-Fhip2b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492839	M	MP:0000266	abnormal heart morphology	Fhip2b<em1(IMPC)Ccpcz>/Fhip2b<em1(IMPC)Ccpcz>	C57BL/6N-Fhip2b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492840	F	MP:0002941	increased circulating alanine transaminase level	Fam199x<em1(IMPC)Mbp>/Fam199x<em1(IMPC)Mbp>	C57BL/6N-Fam199x<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492840	F	MP:0005343	increased circulating aspartate transaminase level	Fam199x<em1(IMPC)Mbp>/Fam199x<em1(IMPC)Mbp>	C57BL/6N-Fam199x<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492840	F	MP:0004906	enlarged uterus	Fam199x<em1(IMPC)Mbp>/Fam199x<em1(IMPC)Mbp>	C57BL/6N-Fam199x<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492841	F	MP:0001284	absent vibrissae	Fam222a<em1(IMPC)J>/Fam222a<em1(IMPC)J>	C57BL/6NJ-Fam222a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492841	F	MP:0000195	decreased circulating calcium level	Fam222a<em1(IMPC)J>/Fam222a<em1(IMPC)J>	C57BL/6NJ-Fam222a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492842	M	MP:0001417	decreased exploration in new environment	Fam53c<em1(IMPC)J>/Fam53c<em1(IMPC)J>	C57BL/6NJ-Fam53c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492843	F	MP:0003604	single kidney	Garin1b<em1(IMPC)Ccpcz>/Garin1b<em1(IMPC)Ccpcz>	C57BL/6N-Garin1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492843	M	MP:0001146	abnormal testis morphology	Garin1b<em1(IMPC)Ccpcz>/Garin1b<em1(IMPC)Ccpcz>	C57BL/6N-Garin1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492843	M	MP:0005627	increased circulating potassium level	Garin1b<em1(IMPC)Ccpcz>/Garin1b<em1(IMPC)Ccpcz>	C57BL/6N-Garin1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492843	F	MP:0000709	enlarged thymus	Garin1b<em1(IMPC)Ccpcz>/Garin1b<em1(IMPC)Ccpcz>	C57BL/6N-Garin1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492843	F	MP:0000703	abnormal thymus morphology	Garin1b<em1(IMPC)Ccpcz>/Garin1b<em1(IMPC)Ccpcz>	C57BL/6N-Garin1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492843	M	MP:0001147	small testis	Garin1b<em1(IMPC)Ccpcz>/Garin1b<em1(IMPC)Ccpcz>	C57BL/6N-Garin1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492843	F	MP:0000274	enlarged heart	Garin1b<em1(IMPC)Ccpcz>/Garin1b<em1(IMPC)Ccpcz>	C57BL/6N-Garin1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492843	F	MP:0000266	abnormal heart morphology	Garin1b<em1(IMPC)Ccpcz>/Garin1b<em1(IMPC)Ccpcz>	C57BL/6N-Garin1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	M	MP:0004599	abnormal vertebral arch morphology	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	F	MP:0000709	enlarged thymus	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	M	MP:0011874	enlarged urinary bladder	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	M	MP:0004924	abnormal behavior	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	M	MP:0000691	enlarged spleen	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	F	MP:0008935	decreased mean platelet volume	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	M	MP:0000274	enlarged heart	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	M	MP:0000702	enlarged lymph nodes	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	F	MP:0002060	abnormal skin morphology	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	M	MP:0000689	abnormal spleen morphology	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	M	MP:0002339	abnormal lymph node morphology	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	M	MP:0000538	abnormal urinary bladder morphology	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	F	MP:0000703	abnormal thymus morphology	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	M	MP:0001402	decreased locomotor activity	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	M	MP:0000266	abnormal heart morphology	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492845	M	MP:0020870	decreased thigmotaxis	Fbxo25<em1(IMPC)Ccpcz>/Fbxo25<em1(IMPC)Ccpcz>	C57BL/6N-Fbxo25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492846	F	MP:0000691	enlarged spleen	Fbxw16<em1(IMPC)Ccpcz>/Fbxw16<+>	C57BL/6N-Fbxw16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492846	M	MP:0013436	increased CD8-positive, naive alpha-beta T cell number	Fbxw16<em1(IMPC)Ccpcz>/Fbxw16<+>	C57BL/6N-Fbxw16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492846	F	MP:0001120	abnormal uterus morphology	Fbxw16<em1(IMPC)Ccpcz>/Fbxw16<+>	C57BL/6N-Fbxw16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492846	F	MP:0000689	abnormal spleen morphology	Fbxw16<em1(IMPC)Ccpcz>/Fbxw16<+>	C57BL/6N-Fbxw16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492846	F	MP:0002100	abnormal tooth morphology	Fbxw16<em1(IMPC)Ccpcz>/Fbxw16<+>	C57BL/6N-Fbxw16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492846	M	MP:0000706	small thymus	Fbxw16<em1(IMPC)Ccpcz>/Fbxw16<+>	C57BL/6N-Fbxw16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492846	F	MP:0000709	enlarged thymus	Fbxw16<em1(IMPC)Ccpcz>/Fbxw16<+>	C57BL/6N-Fbxw16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492848	F	MP:0000691	enlarged spleen	Fbxw20<em1(IMPC)Ccpcz>/Fbxw20<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492848	M	MP:0000702	enlarged lymph nodes	Fbxw20<em1(IMPC)Ccpcz>/Fbxw20<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492848	F	MP:0002060	abnormal skin morphology	Fbxw20<em1(IMPC)Ccpcz>/Fbxw20<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492848	F	MP:0000709	enlarged thymus	Fbxw20<em1(IMPC)Ccpcz>/Fbxw20<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492848	F	MP:0000703	abnormal thymus morphology	Fbxw20<em1(IMPC)Ccpcz>/Fbxw20<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492848	M	MP:0000627	abnormal mammary gland morphology	Fbxw20<em1(IMPC)Ccpcz>/Fbxw20<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492848	M	MP:0002339	abnormal lymph node morphology	Fbxw20<em1(IMPC)Ccpcz>/Fbxw20<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492850	M	MP:0000221	decreased leukocyte cell number	Fgd3<em1(IMPC)Ccpcz>/Fgd3<em1(IMPC)Ccpcz>	C57BL/6N-Fgd3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492850	M	MP:0001417	decreased exploration in new environment	Fgd3<em1(IMPC)Ccpcz>/Fgd3<em1(IMPC)Ccpcz>	C57BL/6N-Fgd3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492850	M	MP:0001146	abnormal testis morphology	Fgd3<em1(IMPC)Ccpcz>/Fgd3<em1(IMPC)Ccpcz>	C57BL/6N-Fgd3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492850	M	MP:0005016	decreased lymphocyte cell number	Fgd3<em1(IMPC)Ccpcz>/Fgd3<em1(IMPC)Ccpcz>	C57BL/6N-Fgd3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492850	M	MP:0001147	small testis	Fgd3<em1(IMPC)Ccpcz>/Fgd3<em1(IMPC)Ccpcz>	C57BL/6N-Fgd3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492850	M	MP:0002059	abnormal seminal vesicle morphology	Fgd3<em1(IMPC)Ccpcz>/Fgd3<em1(IMPC)Ccpcz>	C57BL/6N-Fgd3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492850	F	MP:0005554	decreased circulating creatinine level	Fgd3<em1(IMPC)Ccpcz>/Fgd3<em1(IMPC)Ccpcz>	C57BL/6N-Fgd3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492851	M	MP:0000111	cleft palate	Fgfr1op2<em1(IMPC)Mbp>/Fgfr1op2<em1(IMPC)Mbp>	C57BL/6N-Fgfr1op2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492851	M	MP:0001614	abnormal blood vessel morphology	Fgfr1op2<em1(IMPC)Mbp>/Fgfr1op2<em1(IMPC)Mbp>	C57BL/6N-Fgfr1op2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492851	M	MP:0004258	abnormal placenta size	Fgfr1op2<em1(IMPC)Mbp>/Fgfr1op2<em1(IMPC)Mbp>	C57BL/6N-Fgfr1op2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492853	F	MP:0001126	abnormal ovary morphology	Fmo3<em1(IMPC)Mbp>/Fmo3<em1(IMPC)Mbp>	C57BL/6N-Fmo3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492853	M	MP:0001293	anophthalmia	Fmo3<em1(IMPC)Mbp>/Fmo3<em1(IMPC)Mbp>	C57BL/6N-Fmo3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492853	F	MP:0004832	enlarged ovary	Fmo3<em1(IMPC)Mbp>/Fmo3<em1(IMPC)Mbp>	C57BL/6N-Fmo3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492853	F	MP:0001399	hyperactivity	Fmo3<em1(IMPC)Mbp>/Fmo3<em1(IMPC)Mbp>	C57BL/6N-Fmo3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492853	F	MP:0000703	abnormal thymus morphology	Fmo3<em1(IMPC)Mbp>/Fmo3<em1(IMPC)Mbp>	C57BL/6N-Fmo3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492853	F	MP:0000709	enlarged thymus	Fmo3<em1(IMPC)Mbp>/Fmo3<em1(IMPC)Mbp>	C57BL/6N-Fmo3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492853	F	MP:0000691	enlarged spleen	Fmo3<em1(IMPC)Mbp>/Fmo3<em1(IMPC)Mbp>	C57BL/6N-Fmo3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492853	F	MP:0000689	abnormal spleen morphology	Fmo3<em1(IMPC)Mbp>/Fmo3<em1(IMPC)Mbp>	C57BL/6N-Fmo3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492854	F	MP:0002968	increased circulating alkaline phosphatase level	Fnbp1<em1(IMPC)J>/Fnbp1<em1(IMPC)J>	C57BL/6NJ-Fnbp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492856	F	MP:0005344	increased circulating bilirubin level	Gabpa<em2(IMPC)Mbp>/Gabpa<+>	C57BL/6N-Gabpa<em2(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6492860	M	MP:0011874	enlarged urinary bladder	Ggh<em1(IMPC)Tcp>/Ggh<em1(IMPC)Tcp>	C57BL/6N-Ggh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492860	F	MP:0002637	small uterus	Ggh<em1(IMPC)Tcp>/Ggh<em1(IMPC)Tcp>	C57BL/6N-Ggh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492860	M	MP:0000702	enlarged lymph nodes	Ggh<em1(IMPC)Tcp>/Ggh<em1(IMPC)Tcp>	C57BL/6N-Ggh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492862	F	MP:0000367	abnormal coat/ hair morphology	Gls2<em1(IMPC)Tcp>/Gls2<em1(IMPC)Tcp>	C57BL/6N-Gls2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492862	F	MP:0000157	abnormal sternum morphology	Gls2<em1(IMPC)Tcp>/Gls2<em1(IMPC)Tcp>	C57BL/6N-Gls2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492862	M	MP:0005505	thrombocytosis	Gls2<em1(IMPC)Tcp>/Gls2<em1(IMPC)Tcp>	C57BL/6N-Gls2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492862	F	MP:0001120	abnormal uterus morphology	Gls2<em1(IMPC)Tcp>/Gls2<em1(IMPC)Tcp>	C57BL/6N-Gls2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492862	M	MP:0011874	enlarged urinary bladder	Gls2<em1(IMPC)Tcp>/Gls2<em1(IMPC)Tcp>	C57BL/6N-Gls2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492862	M	MP:0000702	enlarged lymph nodes	Gls2<em1(IMPC)Tcp>/Gls2<em1(IMPC)Tcp>	C57BL/6N-Gls2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492862	F	MP:0001126	abnormal ovary morphology	Gls2<em1(IMPC)Tcp>/Gls2<em1(IMPC)Tcp>	C57BL/6N-Gls2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492862	F	MP:0002060	abnormal skin morphology	Gls2<em1(IMPC)Tcp>/Gls2<em1(IMPC)Tcp>	C57BL/6N-Gls2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492862	M	MP:0000691	enlarged spleen	Gls2<em1(IMPC)Tcp>/Gls2<em1(IMPC)Tcp>	C57BL/6N-Gls2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492862	M	MP:0000598	abnormal liver morphology	Gls2<em1(IMPC)Tcp>/Gls2<em1(IMPC)Tcp>	C57BL/6N-Gls2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492864	F	MP:0008528	polycystic kidney	Glyr1<em1(IMPC)Tcp>/Glyr1<em1(IMPC)Tcp>	C57BL/6N-Glyr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492864	M	MP:0006243	impaired pupillary reflex	Glyr1<em1(IMPC)Tcp>/Glyr1<em1(IMPC)Tcp>	C57BL/6N-Glyr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492864	F	MP:0002764	short tibia	Glyr1<em1(IMPC)Tcp>/Glyr1<em1(IMPC)Tcp>	C57BL/6N-Glyr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492864	M	MP:0000702	enlarged lymph nodes	Glyr1<em1(IMPC)Tcp>/Glyr1<em1(IMPC)Tcp>	C57BL/6N-Glyr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492866	F	MP:0001258	decreased body length	Gnaz<tm1.1(KOMP)Vlcg>/Gnaz<+>	C57BL/6N-Gnaz<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6492866	M	MP:0002060	abnormal skin morphology	Gnaz<tm1.1(KOMP)Vlcg>/Gnaz<+>	C57BL/6N-Gnaz<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6492867	M	MP:0002151	abnormal neural tube morphology	Gne<em1(IMPC)Mbp>/Gne<em1(IMPC)Mbp>	C57BL/6N-Gne<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492869	M	MP:0002075	abnormal coat/hair pigmentation	Gtpbp4<em1(IMPC)Tcp>/Gtpbp4<+>	C57BL/6N-Gtpbp4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492869	F	MP:0002591	decreased mean corpuscular volume	Gtpbp4<em1(IMPC)Tcp>/Gtpbp4<+>	C57BL/6N-Gtpbp4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492873	F	MP:0001297	microphthalmia	Hacd3<em1(IMPC)Mbp>/Hacd3<em1(IMPC)Mbp>	C57BL/6N-Hacd3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492873	M	MP:0001489	decreased startle reflex	Hacd3<em1(IMPC)Mbp>/Hacd3<em1(IMPC)Mbp>	C57BL/6N-Hacd3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492873	M	MP:0011110	preweaning lethality, incomplete penetrance	Hacd3<em1(IMPC)Mbp>/Hacd3<em1(IMPC)Mbp>	C57BL/6N-Hacd3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492873	F	MP:0001293	anophthalmia	Hacd3<em1(IMPC)Mbp>/Hacd3<em1(IMPC)Mbp>	C57BL/6N-Hacd3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492873	F	MP:0001120	abnormal uterus morphology	Hacd3<em1(IMPC)Mbp>/Hacd3<em1(IMPC)Mbp>	C57BL/6N-Hacd3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492873	M	MP:0001304	cataract	Hacd3<em1(IMPC)Mbp>/Hacd3<em1(IMPC)Mbp>	C57BL/6N-Hacd3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492873	F	MP:0000601	small liver	Hacd3<em1(IMPC)Mbp>/Hacd3<em1(IMPC)Mbp>	C57BL/6N-Hacd3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492873	F	MP:0002092	abnormal eye morphology	Hacd3<em1(IMPC)Mbp>/Hacd3<em1(IMPC)Mbp>	C57BL/6N-Hacd3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492873	M	MP:0000599	enlarged liver	Hacd3<em1(IMPC)Mbp>/Hacd3<em1(IMPC)Mbp>	C57BL/6N-Hacd3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492875	M	MP:0008044	increased NK cell number	Hdac4<em1(IMPC)Ccpcz>/Hdac4<+>	C57BL/6N-Hdac4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492875	F	MP:0002968	increased circulating alkaline phosphatase level	Hdac4<em1(IMPC)Ccpcz>/Hdac4<+>	C57BL/6N-Hdac4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492877	M	MP:0010024	increased total body fat amount	Heca<em1(IMPC)J>/Heca<em1(IMPC)J>	C57BL/6NJ-Heca<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492877	M	MP:0001556	increased circulating HDL cholesterol level	Heca<em1(IMPC)J>/Heca<em1(IMPC)J>	C57BL/6NJ-Heca<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492877	M	MP:0003961	decreased lean body mass	Heca<em1(IMPC)J>/Heca<em1(IMPC)J>	C57BL/6NJ-Heca<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492877	M	MP:0005178	increased circulating cholesterol level	Heca<em1(IMPC)J>/Heca<em1(IMPC)J>	C57BL/6NJ-Heca<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492878	M	MP:0000691	enlarged spleen	Helq<em1(IMPC)Mbp>/Helq<em1(IMPC)Mbp>	C57BL/6N-Helq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492878	M	MP:0000689	abnormal spleen morphology	Helq<em1(IMPC)Mbp>/Helq<em1(IMPC)Mbp>	C57BL/6N-Helq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492878	F	MP:0002135	abnormal kidney morphology	Helq<em1(IMPC)Mbp>/Helq<em1(IMPC)Mbp>	C57BL/6N-Helq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492878	M	MP:0001146	abnormal testis morphology	Helq<em1(IMPC)Mbp>/Helq<em1(IMPC)Mbp>	C57BL/6N-Helq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492878	F	MP:0010024	increased total body fat amount	Helq<em1(IMPC)Mbp>/Helq<em1(IMPC)Mbp>	C57BL/6N-Helq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492878	F	MP:0002092	abnormal eye morphology	Helq<em1(IMPC)Mbp>/Helq<em1(IMPC)Mbp>	C57BL/6N-Helq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492878	F	MP:0001926	female infertility	Helq<em1(IMPC)Mbp>/Helq<em1(IMPC)Mbp>	C57BL/6N-Helq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492878	F	MP:0003961	decreased lean body mass	Helq<em1(IMPC)Mbp>/Helq<em1(IMPC)Mbp>	C57BL/6N-Helq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492878	M	MP:0001147	small testis	Helq<em1(IMPC)Mbp>/Helq<em1(IMPC)Mbp>	C57BL/6N-Helq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492878	M	MP:0001925	male infertility	Helq<em1(IMPC)Mbp>/Helq<em1(IMPC)Mbp>	C57BL/6N-Helq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492878	F	MP:0002989	small kidney	Helq<em1(IMPC)Mbp>/Helq<em1(IMPC)Mbp>	C57BL/6N-Helq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492878	F	MP:0010124	decreased bone mineral content	Helq<em1(IMPC)Mbp>/Helq<em1(IMPC)Mbp>	C57BL/6N-Helq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492883	F	MP:0005343	increased circulating aspartate transaminase level	Hivep1<tm1(KOMP)Mbp>/Hivep1<+>	C57BL/6N-Hivep1<tm1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492883	M	MP:0000274	enlarged heart	Hivep1<tm1(KOMP)Mbp>/Hivep1<+>	C57BL/6N-Hivep1<tm1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492883	M	MP:0000266	abnormal heart morphology	Hivep1<tm1(KOMP)Mbp>/Hivep1<+>	C57BL/6N-Hivep1<tm1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492883	F	MP:0002941	increased circulating alanine transaminase level	Hivep1<tm1(KOMP)Mbp>/Hivep1<+>	C57BL/6N-Hivep1<tm1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492883	M	MP:0002606	increased basophil cell number	Hivep1<tm1(KOMP)Mbp>/Hivep1<+>	C57BL/6N-Hivep1<tm1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492885	F	MP:0010392	prolonged QRS complex duration	Homer2<em1(IMPC)J>/Homer2<em1(IMPC)J>	C57BL/6NJ-Homer2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492887	F	MP:0001566	increased circulating phosphate level	Hspb8<em1(IMPC)J>/Hspb8<em1(IMPC)J>	C57BL/6NJ-Hspb8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492887	F	MP:0000221	decreased leukocyte cell number	Hspb8<em1(IMPC)J>/Hspb8<em1(IMPC)J>	C57BL/6NJ-Hspb8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492887	M	MP:0000367	abnormal coat/ hair morphology	Hspb8<em1(IMPC)J>/Hspb8<em1(IMPC)J>	C57BL/6NJ-Hspb8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492887	F	MP:0001399	hyperactivity	Hspb8<em1(IMPC)J>/Hspb8<em1(IMPC)J>	C57BL/6NJ-Hspb8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492891	F	MP:0010092	increased circulating magnesium level	Ifih1<em1(IMPC)Wtsi>/Ifih1<em1(IMPC)Wtsi>	C57BL/6N-Ifih1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6492893	M	MP:0002997	enlarged seminal vesicle	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492893	M	MP:0002339	abnormal lymph node morphology	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492893	M	MP:0001447	abnormal nest building behavior	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	38370417
MGI:6492893	M	MP:0009710	anhedonia	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	38370417
MGI:6492893	F	MP:0001399	hyperactivity	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	38370417
MGI:6492893	F	MP:0002092	abnormal eye morphology	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492893	M	MP:0000598	abnormal liver morphology	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492893	F	MP:0002574	increased vertical activity	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	38370417
MGI:6492893	F	MP:0000691	enlarged spleen	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492893	F	MP:0002060	abnormal skin morphology	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492893	M	MP:0020379	abnormal sucrose solution preference	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	38370417
MGI:6492893	M	MP:0001525	impaired balance	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	38370417
MGI:6492893	M	MP:0000702	enlarged lymph nodes	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492893	F	MP:0003068	enlarged kidney	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492893	F	MP:0000689	abnormal spleen morphology	Iglon5<em1(IMPC)Mbp>/Iglon5<em1(IMPC)Mbp>	C57BL/6NCrl-Iglon5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6492895	F	MP:0005293	impaired glucose tolerance	Insig1<em1(IMPC)Ccpcz>/Insig1<em1(IMPC)Ccpcz>	C57BL/6N-Insig1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492895	F	MP:0005278	abnormal cholesterol homeostasis	Insig1<em1(IMPC)Ccpcz>/Insig1<em1(IMPC)Ccpcz>	C57BL/6N-Insig1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492895	F	MP:0001262	decreased body weight	Insig1<em1(IMPC)Ccpcz>/Insig1<em1(IMPC)Ccpcz>	C57BL/6N-Insig1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492895	F	MP:0000538	abnormal urinary bladder morphology	Insig1<em1(IMPC)Ccpcz>/Insig1<em1(IMPC)Ccpcz>	C57BL/6N-Insig1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492895	F	MP:0005655	increased aggression	Insig1<em1(IMPC)Ccpcz>/Insig1<em1(IMPC)Ccpcz>	C57BL/6N-Insig1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492895	M	MP:0020421	increased freezing behavior	Insig1<em1(IMPC)Ccpcz>/Insig1<em1(IMPC)Ccpcz>	C57BL/6N-Insig1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492896	F	MP:0005333	decreased heart rate	Insig2<em1(IMPC)Hmgu>/Insig2<em1(IMPC)Hmgu>	C57BL/6N-Insig2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6492898	M	MP:0001697	abnormal embryo size	Ipo4<em1(IMPC)J>/Ipo4<em1(IMPC)J>	C57BL/6NJ-Ipo4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492898	F	MP:0003984	embryonic growth retardation	Ipo4<em1(IMPC)J>/Ipo4<em1(IMPC)J>	C57BL/6NJ-Ipo4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492899	M	MP:0001488	increased startle reflex	Irgc<em1(IMPC)Tcp>/Irgc<em1(IMPC)Tcp>	C57BL/6N-Irgc<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492899	F	MP:0001289	persistence of hyaloid vascular system	Irgc<em1(IMPC)Tcp>/Irgc<em1(IMPC)Tcp>	C57BL/6N-Irgc<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492899	M	MP:0002092	abnormal eye morphology	Irgc<em1(IMPC)Tcp>/Irgc<em1(IMPC)Tcp>	C57BL/6N-Irgc<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492899	M	MP:0000220	increased monocyte cell number	Irgc<em1(IMPC)Tcp>/Irgc<em1(IMPC)Tcp>	C57BL/6N-Irgc<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492899	M	MP:0001925	male infertility	Irgc<em1(IMPC)Tcp>/Irgc<em1(IMPC)Tcp>	C57BL/6N-Irgc<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492900	M	MP:0005333	decreased heart rate	Ist1<em1(IMPC)J>/Ist1<+>	C57BL/6NJ-Ist1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492900	M	MP:0010506	prolonged RR interval	Ist1<em1(IMPC)J>/Ist1<+>	C57BL/6NJ-Ist1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492901	F	MP:0001417	decreased exploration in new environment	Itsn1<em1(IMPC)H>/Itsn1<+>	C57BL/6NTac-Itsn1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492902	F	MP:0008810	increased circulating iron level	Itsn1<em1(IMPC)H>/Itsn1<em1(IMPC)H>	C57BL/6NTac-Itsn1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492902	F	MP:0011239	abnormal skin coloration	Itsn1<em1(IMPC)H>/Itsn1<em1(IMPC)H>	C57BL/6NTac-Itsn1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492902	F	MP:0001406	abnormal gait	Itsn1<em1(IMPC)H>/Itsn1<em1(IMPC)H>	C57BL/6NTac-Itsn1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492902	M	MP:0002965	increased circulating serum albumin level	Itsn1<em1(IMPC)H>/Itsn1<em1(IMPC)H>	C57BL/6NTac-Itsn1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492902	M	MP:0008806	increased circulating amylase level	Itsn1<em1(IMPC)H>/Itsn1<em1(IMPC)H>	C57BL/6NTac-Itsn1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492902	M	MP:0001513	limb grasping	Itsn1<em1(IMPC)H>/Itsn1<em1(IMPC)H>	C57BL/6NTac-Itsn1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492904	F	MP:0002968	increased circulating alkaline phosphatase level	Jmjd4<em1(IMPC)Wtsi>/Jmjd4<em1(IMPC)Wtsi>	C57BL/6N-Jmjd4<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6492904	M	MP:0010025	decreased total body fat amount	Jmjd4<em1(IMPC)Wtsi>/Jmjd4<em1(IMPC)Wtsi>	C57BL/6N-Jmjd4<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6492904	M	MP:0005561	increased mean corpuscular hemoglobin	Jmjd4<em1(IMPC)Wtsi>/Jmjd4<em1(IMPC)Wtsi>	C57BL/6N-Jmjd4<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6492904	M	MP:0003960	increased lean body mass	Jmjd4<em1(IMPC)Wtsi>/Jmjd4<em1(IMPC)Wtsi>	C57BL/6N-Jmjd4<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6492904	M	MP:0013278	decreased fasting circulating glucose level	Jmjd4<em1(IMPC)Wtsi>/Jmjd4<em1(IMPC)Wtsi>	C57BL/6N-Jmjd4<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6492904	M	MP:0010088	decreased circulating fructosamine level	Jmjd4<em1(IMPC)Wtsi>/Jmjd4<em1(IMPC)Wtsi>	C57BL/6N-Jmjd4<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6492905	F	MP:0020870	decreased thigmotaxis	Kcnf1<em1(IMPC)H>/Kcnf1<em1(IMPC)H>	C57BL/6N-Kcnf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492905	F	MP:0001364	decreased anxiety-related response	Kcnf1<em1(IMPC)H>/Kcnf1<em1(IMPC)H>	C57BL/6N-Kcnf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492905	F	MP:0004924	abnormal behavior	Kcnf1<em1(IMPC)H>/Kcnf1<em1(IMPC)H>	C57BL/6N-Kcnf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492905	F	MP:0001402	decreased locomotor activity	Kcnf1<em1(IMPC)H>/Kcnf1<em1(IMPC)H>	C57BL/6N-Kcnf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6492906	F	MP:0002606	increased basophil cell number	Kcnj9<tm1b(EUCOMM)Hmgu>/Kcnj9<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kcnj9<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6492907	M	MP:0000702	enlarged lymph nodes	Kcnmb4<em1(IMPC)Mbp>/Kcnmb4<em1(IMPC)Mbp>	C57BL/6N-Kcnmb4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492907	M	MP:0002339	abnormal lymph node morphology	Kcnmb4<em1(IMPC)Mbp>/Kcnmb4<em1(IMPC)Mbp>	C57BL/6N-Kcnmb4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492911	F	MP:0011962	increased cornea thickness	Kifc3<tm1b(EUCOMM)Hmgu>/Kifc3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Kifc3<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6492913	M	MP:0003961	decreased lean body mass	Klhl22<em1(IMPC)J>/Klhl22<em1(IMPC)J>	C57BL/6NJ-Klhl22<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492915	F	MP:0000709	enlarged thymus	Klk11<em1(IMPC)Ccpcz>/Klk11<em1(IMPC)Ccpcz>	C57BL/6N-Klk11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492915	F	MP:0000703	abnormal thymus morphology	Klk11<em1(IMPC)Ccpcz>/Klk11<em1(IMPC)Ccpcz>	C57BL/6N-Klk11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492915	M	MP:0000598	abnormal liver morphology	Klk11<em1(IMPC)Ccpcz>/Klk11<em1(IMPC)Ccpcz>	C57BL/6N-Klk11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492915	F	MP:0002060	abnormal skin morphology	Klk11<em1(IMPC)Ccpcz>/Klk11<em1(IMPC)Ccpcz>	C57BL/6N-Klk11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492915	M	MP:0000438	abnormal cranium morphology	Klk11<em1(IMPC)Ccpcz>/Klk11<em1(IMPC)Ccpcz>	C57BL/6N-Klk11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492915	M	MP:0001146	abnormal testis morphology	Klk11<em1(IMPC)Ccpcz>/Klk11<em1(IMPC)Ccpcz>	C57BL/6N-Klk11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492915	M	MP:0002059	abnormal seminal vesicle morphology	Klk11<em1(IMPC)Ccpcz>/Klk11<em1(IMPC)Ccpcz>	C57BL/6N-Klk11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492916	M	MP:0002932	abnormal joint morphology	Klk15<em1(IMPC)Ccpcz>/Klk15<em1(IMPC)Ccpcz>	C57BL/6N-Klk15<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492916	M	MP:0001402	decreased locomotor activity	Klk15<em1(IMPC)Ccpcz>/Klk15<em1(IMPC)Ccpcz>	C57BL/6N-Klk15<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492916	F	MP:0000367	abnormal coat/ hair morphology	Klk15<em1(IMPC)Ccpcz>/Klk15<em1(IMPC)Ccpcz>	C57BL/6N-Klk15<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492919	M	MP:0000702	enlarged lymph nodes	Krt27<em1(IMPC)Ccpcz>/Krt27<em1(IMPC)Ccpcz>	C57BL/6N-Krt27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492919	F	MP:0002060	abnormal skin morphology	Krt27<em1(IMPC)Ccpcz>/Krt27<em1(IMPC)Ccpcz>	C57BL/6N-Krt27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492919	M	MP:0002339	abnormal lymph node morphology	Krt27<em1(IMPC)Ccpcz>/Krt27<em1(IMPC)Ccpcz>	C57BL/6N-Krt27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492919	M	MP:0000266	abnormal heart morphology	Krt27<em1(IMPC)Ccpcz>/Krt27<em1(IMPC)Ccpcz>	C57BL/6N-Krt27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492919	M	MP:0002059	abnormal seminal vesicle morphology	Krt27<em1(IMPC)Ccpcz>/Krt27<em1(IMPC)Ccpcz>	C57BL/6N-Krt27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492919	M	MP:0000274	enlarged heart	Krt27<em1(IMPC)Ccpcz>/Krt27<em1(IMPC)Ccpcz>	C57BL/6N-Krt27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492919	M	MP:0000162	lordosis	Krt27<em1(IMPC)Ccpcz>/Krt27<em1(IMPC)Ccpcz>	C57BL/6N-Krt27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492920	M	MP:0000702	enlarged lymph nodes	Krt28<em1(IMPC)Ccpcz>/Krt28<em1(IMPC)Ccpcz>	C57BL/6N-Krt28<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492920	M	MP:0002339	abnormal lymph node morphology	Krt28<em1(IMPC)Ccpcz>/Krt28<em1(IMPC)Ccpcz>	C57BL/6N-Krt28<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492920	M	MP:0002059	abnormal seminal vesicle morphology	Krt28<em1(IMPC)Ccpcz>/Krt28<em1(IMPC)Ccpcz>	C57BL/6N-Krt28<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492921	F	MP:0000703	abnormal thymus morphology	Krt33a<em1(IMPC)Ccpcz>/Krt33a<em1(IMPC)Ccpcz>	C57BL/6N-Krt33a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492921	F	MP:0000709	enlarged thymus	Krt33a<em1(IMPC)Ccpcz>/Krt33a<em1(IMPC)Ccpcz>	C57BL/6N-Krt33a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492921	F	MP:0011047	increased lung tissue damping	Krt33a<em1(IMPC)Ccpcz>/Krt33a<em1(IMPC)Ccpcz>	C57BL/6N-Krt33a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492922	F	MP:0005011	increased eosinophil cell number	Krt33b<em1(IMPC)Ccpcz>/Krt33b<em1(IMPC)Ccpcz>	C57BL/6N-Krt33b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492922	F	MP:0000709	enlarged thymus	Krt33b<em1(IMPC)Ccpcz>/Krt33b<em1(IMPC)Ccpcz>	C57BL/6N-Krt33b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492922	F	MP:0000703	abnormal thymus morphology	Krt33b<em1(IMPC)Ccpcz>/Krt33b<em1(IMPC)Ccpcz>	C57BL/6N-Krt33b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492922	M	MP:0001147	small testis	Krt33b<em1(IMPC)Ccpcz>/Krt33b<em1(IMPC)Ccpcz>	C57BL/6N-Krt33b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492922	F	MP:0002135	abnormal kidney morphology	Krt33b<em1(IMPC)Ccpcz>/Krt33b<em1(IMPC)Ccpcz>	C57BL/6N-Krt33b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492922	F	MP:0003604	single kidney	Krt33b<em1(IMPC)Ccpcz>/Krt33b<em1(IMPC)Ccpcz>	C57BL/6N-Krt33b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492922	M	MP:0001146	abnormal testis morphology	Krt33b<em1(IMPC)Ccpcz>/Krt33b<em1(IMPC)Ccpcz>	C57BL/6N-Krt33b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492924	M	MP:0001200	thick skin	Krt86<em1(IMPC)Tcp>/Krt86<em1(IMPC)Tcp>	C57BL/6N-Krt86<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492925	F	MP:0008040	decreased NK T cell number	Krtap8-1<em1(IMPC)Ccpcz>/Krtap8-1<em1(IMPC)Ccpcz>	C57BL/6N-Krtap8-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492925	F	MP:0001489	decreased startle reflex	Krtap8-1<em1(IMPC)Ccpcz>/Krtap8-1<em1(IMPC)Ccpcz>	C57BL/6N-Krtap8-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492925	M	MP:0000266	abnormal heart morphology	Krtap8-1<em1(IMPC)Ccpcz>/Krtap8-1<em1(IMPC)Ccpcz>	C57BL/6N-Krtap8-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492925	F	MP:0000162	lordosis	Krtap8-1<em1(IMPC)Ccpcz>/Krtap8-1<em1(IMPC)Ccpcz>	C57BL/6N-Krtap8-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492925	M	MP:0001262	decreased body weight	Krtap8-1<em1(IMPC)Ccpcz>/Krtap8-1<em1(IMPC)Ccpcz>	C57BL/6N-Krtap8-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492925	M	MP:0001417	decreased exploration in new environment	Krtap8-1<em1(IMPC)Ccpcz>/Krtap8-1<em1(IMPC)Ccpcz>	C57BL/6N-Krtap8-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492925	M	MP:0000274	enlarged heart	Krtap8-1<em1(IMPC)Ccpcz>/Krtap8-1<em1(IMPC)Ccpcz>	C57BL/6N-Krtap8-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492925	F	MP:0001120	abnormal uterus morphology	Krtap8-1<em1(IMPC)Ccpcz>/Krtap8-1<em1(IMPC)Ccpcz>	C57BL/6N-Krtap8-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492925	F	MP:0009709	hydrometra	Krtap8-1<em1(IMPC)Ccpcz>/Krtap8-1<em1(IMPC)Ccpcz>	C57BL/6N-Krtap8-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492925	M	MP:0001325	abnormal retina morphology	Krtap8-1<em1(IMPC)Ccpcz>/Krtap8-1<em1(IMPC)Ccpcz>	C57BL/6N-Krtap8-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492926	M	MP:0001489	decreased startle reflex	Krtcap2<em1(IMPC)J>/Krtcap2<em1(IMPC)J>	C57BL/6NJ-Krtcap2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492926	M	MP:0005635	decreased circulating bilirubin level	Krtcap2<em1(IMPC)J>/Krtcap2<em1(IMPC)J>	C57BL/6NJ-Krtcap2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492926	F	MP:0020870	decreased thigmotaxis	Krtcap2<em1(IMPC)J>/Krtcap2<em1(IMPC)J>	C57BL/6NJ-Krtcap2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492926	F	MP:0001402	decreased locomotor activity	Krtcap2<em1(IMPC)J>/Krtcap2<em1(IMPC)J>	C57BL/6NJ-Krtcap2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492926	M	MP:0005293	impaired glucose tolerance	Krtcap2<em1(IMPC)J>/Krtcap2<em1(IMPC)J>	C57BL/6NJ-Krtcap2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492926	F	MP:0004924	abnormal behavior	Krtcap2<em1(IMPC)J>/Krtcap2<em1(IMPC)J>	C57BL/6NJ-Krtcap2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492926	F	MP:0002574	increased vertical activity	Krtcap2<em1(IMPC)J>/Krtcap2<em1(IMPC)J>	C57BL/6NJ-Krtcap2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492932	F	MP:0000691	enlarged spleen	Lox<em1(IMPC)Mbp>/Lox<+>	C57BL/6N-Lox<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492932	F	MP:0002989	small kidney	Lox<em1(IMPC)Mbp>/Lox<+>	C57BL/6N-Lox<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492932	F	MP:0002135	abnormal kidney morphology	Lox<em1(IMPC)Mbp>/Lox<+>	C57BL/6N-Lox<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492932	F	MP:0000689	abnormal spleen morphology	Lox<em1(IMPC)Mbp>/Lox<+>	C57BL/6N-Lox<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492932	F	MP:0002060	abnormal skin morphology	Lox<em1(IMPC)Mbp>/Lox<+>	C57BL/6N-Lox<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492936	F	MP:0020421	increased freezing behavior	Ltn1<tm1b(EUCOMM)Hmgu>/Ltn1<+>	C57BL/6N-Ltn1<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6492937	M	MP:0000221	decreased leukocyte cell number	Ltv1<em1(IMPC)J>/Ltv1<+>	C57BL/6NJ-Ltv1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492939	F	MP:0010053	decreased grip strength	Luc7l3<em1(IMPC)J>/Luc7l3<+>	C57BL/6NJ-Luc7l3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492939	M	MP:0002941	increased circulating alanine transaminase level	Luc7l3<em1(IMPC)J>/Luc7l3<+>	C57BL/6NJ-Luc7l3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492939	M	MP:0003131	increased erythrocyte cell number	Luc7l3<em1(IMPC)J>/Luc7l3<+>	C57BL/6NJ-Luc7l3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492941	F	MP:0010052	increased grip strength	Lurap1<em1(IMPC)J>/Lurap1<em1(IMPC)J>	C57BL/6NJ-Lurap1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492941	M	MP:0000367	abnormal coat/ hair morphology	Lurap1<em1(IMPC)J>/Lurap1<em1(IMPC)J>	C57BL/6NJ-Lurap1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492941	M	MP:0001566	increased circulating phosphate level	Lurap1<em1(IMPC)J>/Lurap1<em1(IMPC)J>	C57BL/6NJ-Lurap1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492942	F	MP:0000266	abnormal heart morphology	Ly86<tm1a(KOMP)Wtsi>/Ly86<tm1a(KOMP)Wtsi>	C57BL/6N-Ly86<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6492942	F	MP:0002833	increased heart weight	Ly86<tm1a(KOMP)Wtsi>/Ly86<tm1a(KOMP)Wtsi>	C57BL/6N-Ly86<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6492942	F	MP:0010025	decreased total body fat amount	Ly86<tm1a(KOMP)Wtsi>/Ly86<tm1a(KOMP)Wtsi>	C57BL/6N-Ly86<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6492942	F	MP:0003960	increased lean body mass	Ly86<tm1a(KOMP)Wtsi>/Ly86<tm1a(KOMP)Wtsi>	C57BL/6N-Ly86<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6492942	F	MP:0000218	increased leukocyte cell number	Ly86<tm1a(KOMP)Wtsi>/Ly86<tm1a(KOMP)Wtsi>	C57BL/6N-Ly86<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6492942	F	MP:0000274	enlarged heart	Ly86<tm1a(KOMP)Wtsi>/Ly86<tm1a(KOMP)Wtsi>	C57BL/6N-Ly86<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6492942	F	MP:0005013	increased lymphocyte cell number	Ly86<tm1a(KOMP)Wtsi>/Ly86<tm1a(KOMP)Wtsi>	C57BL/6N-Ly86<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6492943	M	MP:0001402	decreased locomotor activity	Maged1<em1(IMPC)Mbp>/Y	C57BL/6N-Maged1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492943	M	MP:0005333	decreased heart rate	Maged1<em1(IMPC)Mbp>/Y	C57BL/6N-Maged1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492943	M	MP:0010506	prolonged RR interval	Maged1<em1(IMPC)Mbp>/Y	C57BL/6N-Maged1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492945	M	MP:0001925	male infertility	Mapk6<em1(IMPC)Mbp>/Mapk6<em1(IMPC)Mbp>	C57BL/6N-Mapk6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492946	F	MP:0000709	enlarged thymus	Mapkapk3<em1(IMPC)Ccpcz>/Mapkapk3<em1(IMPC)Ccpcz>	C57BL/6N-Mapkapk3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492946	M	MP:0000266	abnormal heart morphology	Mapkapk3<em1(IMPC)Ccpcz>/Mapkapk3<em1(IMPC)Ccpcz>	C57BL/6N-Mapkapk3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492946	M	MP:0000274	enlarged heart	Mapkapk3<em1(IMPC)Ccpcz>/Mapkapk3<em1(IMPC)Ccpcz>	C57BL/6N-Mapkapk3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492946	M	MP:0000689	abnormal spleen morphology	Mapkapk3<em1(IMPC)Ccpcz>/Mapkapk3<em1(IMPC)Ccpcz>	C57BL/6N-Mapkapk3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492946	F	MP:0002060	abnormal skin morphology	Mapkapk3<em1(IMPC)Ccpcz>/Mapkapk3<em1(IMPC)Ccpcz>	C57BL/6N-Mapkapk3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492946	F	MP:0000703	abnormal thymus morphology	Mapkapk3<em1(IMPC)Ccpcz>/Mapkapk3<em1(IMPC)Ccpcz>	C57BL/6N-Mapkapk3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492946	M	MP:0000691	enlarged spleen	Mapkapk3<em1(IMPC)Ccpcz>/Mapkapk3<em1(IMPC)Ccpcz>	C57BL/6N-Mapkapk3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6492947	F	MP:0000703	abnormal thymus morphology	Marchf3<tm1b(EUCOMM)Hmgu>/Marchf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6492947	M	MP:0002135	abnormal kidney morphology	Marchf3<tm1b(EUCOMM)Hmgu>/Marchf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6492947	F	MP:0001120	abnormal uterus morphology	Marchf3<tm1b(EUCOMM)Hmgu>/Marchf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6492947	F	MP:0004906	enlarged uterus	Marchf3<tm1b(EUCOMM)Hmgu>/Marchf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6492947	F	MP:0009453	enhanced contextual conditioning behavior	Marchf3<tm1b(EUCOMM)Hmgu>/Marchf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6492947	M	MP:0000274	enlarged heart	Marchf3<tm1b(EUCOMM)Hmgu>/Marchf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6492947	F	MP:0000709	enlarged thymus	Marchf3<tm1b(EUCOMM)Hmgu>/Marchf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6492947	M	MP:0000691	enlarged spleen	Marchf3<tm1b(EUCOMM)Hmgu>/Marchf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6492947	M	MP:0000266	abnormal heart morphology	Marchf3<tm1b(EUCOMM)Hmgu>/Marchf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6492947	M	MP:0003068	enlarged kidney	Marchf3<tm1b(EUCOMM)Hmgu>/Marchf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6492947	M	MP:0000689	abnormal spleen morphology	Marchf3<tm1b(EUCOMM)Hmgu>/Marchf3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Marchf3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6492949	F	MP:0001120	abnormal uterus morphology	Mctp1<em1(IMPC)Mbp>/Mctp1<em1(IMPC)Mbp>	C57BL/6N-Mctp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492949	F	MP:0009709	hydrometra	Mctp1<em1(IMPC)Mbp>/Mctp1<em1(IMPC)Mbp>	C57BL/6N-Mctp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492950	M	MP:0000691	enlarged spleen	Mcts1<em1(IMPC)Mbp>/Y	C57BL/6N-Mcts1<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:6492952	M	MP:0005293	impaired glucose tolerance	Mettl18<em1(IMPC)J>/Mettl18<em1(IMPC)J>	C57BL/6NJ-Mettl18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492952	M	MP:0003960	increased lean body mass	Mettl18<em1(IMPC)J>/Mettl18<em1(IMPC)J>	C57BL/6NJ-Mettl18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492952	M	MP:0013279	increased fasting circulating glucose level	Mettl18<em1(IMPC)J>/Mettl18<em1(IMPC)J>	C57BL/6NJ-Mettl18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492952	M	MP:0002110	abnormal digit morphology	Mettl18<em1(IMPC)J>/Mettl18<em1(IMPC)J>	C57BL/6NJ-Mettl18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492952	F	MP:0001513	limb grasping	Mettl18<em1(IMPC)J>/Mettl18<em1(IMPC)J>	C57BL/6NJ-Mettl18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492953	M	MP:0000702	enlarged lymph nodes	Mfsd1<em1(IMPC)Tcp>/Mfsd1<+>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492953	M	MP:0001293	anophthalmia	Mfsd1<em1(IMPC)Tcp>/Mfsd1<+>	C57BL/6N-Mfsd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492956	F	MP:0000702	enlarged lymph nodes	Mllt10<em1(IMPC)Mbp>/Mllt10<+>	C57BL/6N-Mllt10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492956	F	MP:0001126	abnormal ovary morphology	Mllt10<em1(IMPC)Mbp>/Mllt10<+>	C57BL/6N-Mllt10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492956	F	MP:0002060	abnormal skin morphology	Mllt10<em1(IMPC)Mbp>/Mllt10<+>	C57BL/6N-Mllt10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492956	F	MP:0002339	abnormal lymph node morphology	Mllt10<em1(IMPC)Mbp>/Mllt10<+>	C57BL/6N-Mllt10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492956	M	MP:0000219	increased neutrophil cell number	Mllt10<em1(IMPC)Mbp>/Mllt10<+>	C57BL/6N-Mllt10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492956	M	MP:0000266	abnormal heart morphology	Mllt10<em1(IMPC)Mbp>/Mllt10<+>	C57BL/6N-Mllt10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492956	M	MP:0000494	abnormal cecum morphology	Mllt10<em1(IMPC)Mbp>/Mllt10<+>	C57BL/6N-Mllt10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492956	M	MP:0000274	enlarged heart	Mllt10<em1(IMPC)Mbp>/Mllt10<+>	C57BL/6N-Mllt10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492956	F	MP:0004832	enlarged ovary	Mllt10<em1(IMPC)Mbp>/Mllt10<+>	C57BL/6N-Mllt10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492956	M	MP:0005016	decreased lymphocyte cell number	Mllt10<em1(IMPC)Mbp>/Mllt10<+>	C57BL/6N-Mllt10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492956	M	MP:0009476	enlarged cecum	Mllt10<em1(IMPC)Mbp>/Mllt10<+>	C57BL/6N-Mllt10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492958	M	MP:0011965	decreased total retina thickness	Mpp2<tm1b(KOMP)Wtsi>/Mpp2<tm1b(KOMP)Wtsi>	C57BL/6N-Mpp2<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6492959	F	MP:0003921	abnormal heart left ventricle morphology	Mpp3<tm1b(EUCOMM)Wtsi>/Mpp3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Mpp3<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6492959	F	MP:0002953	thick ventricular wall	Mpp3<tm1b(EUCOMM)Wtsi>/Mpp3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Mpp3<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6492959	F	MP:0005599	increased cardiac muscle contractility	Mpp3<tm1b(EUCOMM)Wtsi>/Mpp3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Mpp3<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6492960	M	MP:0001417	decreased exploration in new environment	Mpst<tm1b(EUCOMM)Hmgu>/Mpst<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mpst<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6492961	F	MP:0001697	abnormal embryo size	Mrap<em1(IMPC)Tcp>/Mrap<em1(IMPC)Tcp>	C57BL/6N-Mrap<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492964	M	MP:0002631	abnormal epididymis morphology	Ms4a3<tm1.1(KOMP)Vlcg>/Ms4a3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ms4a3<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6492964	M	MP:0000266	abnormal heart morphology	Ms4a3<tm1.1(KOMP)Vlcg>/Ms4a3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ms4a3<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6492964	M	MP:0000274	enlarged heart	Ms4a3<tm1.1(KOMP)Vlcg>/Ms4a3<tm1.1(KOMP)Vlcg>	C57BL/6N-Ms4a3<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6492966	M	MP:0011874	enlarged urinary bladder	Myh8<em1(IMPC)Tcp>/Myh8<+>	C57BL/6N-Myh8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492966	M	MP:0000157	abnormal sternum morphology	Myh8<em1(IMPC)Tcp>/Myh8<+>	C57BL/6N-Myh8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492966	F	MP:0000208	decreased hematocrit	Myh8<em1(IMPC)Tcp>/Myh8<+>	C57BL/6N-Myh8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492967	M	MP:0010024	increased total body fat amount	Mylk4<em1(IMPC)J>/Mylk4<em1(IMPC)J>	C57BL/6NJ-Mylk4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492967	M	MP:0010124	decreased bone mineral content	Mylk4<em1(IMPC)J>/Mylk4<em1(IMPC)J>	C57BL/6NJ-Mylk4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492967	M	MP:0001304	cataract	Mylk4<em1(IMPC)J>/Mylk4<em1(IMPC)J>	C57BL/6NJ-Mylk4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492967	M	MP:0003961	decreased lean body mass	Mylk4<em1(IMPC)J>/Mylk4<em1(IMPC)J>	C57BL/6NJ-Mylk4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492969	M	MP:0002060	abnormal skin morphology	Nans<em1(IMPC)Tcp>/Nans<+>	C57BL/6N-Nans<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492969	M	MP:0010024	increased total body fat amount	Nans<em1(IMPC)Tcp>/Nans<+>	C57BL/6N-Nans<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492969	F	MP:0002092	abnormal eye morphology	Nans<em1(IMPC)Tcp>/Nans<+>	C57BL/6N-Nans<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492969	M	MP:0003961	decreased lean body mass	Nans<em1(IMPC)Tcp>/Nans<+>	C57BL/6N-Nans<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492971	M	MP:0000691	enlarged spleen	Ncoa2<em1(IMPC)Mbp>/Ncoa2<+>	C57BL/6N-Ncoa2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492971	M	MP:0000219	increased neutrophil cell number	Ncoa2<em1(IMPC)Mbp>/Ncoa2<+>	C57BL/6N-Ncoa2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492971	M	MP:0002060	abnormal skin morphology	Ncoa2<em1(IMPC)Mbp>/Ncoa2<+>	C57BL/6N-Ncoa2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492971	F	MP:0002989	small kidney	Ncoa2<em1(IMPC)Mbp>/Ncoa2<+>	C57BL/6N-Ncoa2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492971	F	MP:0002135	abnormal kidney morphology	Ncoa2<em1(IMPC)Mbp>/Ncoa2<+>	C57BL/6N-Ncoa2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492971	M	MP:0020870	decreased thigmotaxis	Ncoa2<em1(IMPC)Mbp>/Ncoa2<+>	C57BL/6N-Ncoa2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492971	M	MP:0004924	abnormal behavior	Ncoa2<em1(IMPC)Mbp>/Ncoa2<+>	C57BL/6N-Ncoa2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492971	M	MP:0001364	decreased anxiety-related response	Ncoa2<em1(IMPC)Mbp>/Ncoa2<+>	C57BL/6N-Ncoa2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492971	M	MP:0002079	increased circulating insulin level	Ncoa2<em1(IMPC)Mbp>/Ncoa2<+>	C57BL/6N-Ncoa2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492971	M	MP:0001402	decreased locomotor activity	Ncoa2<em1(IMPC)Mbp>/Ncoa2<+>	C57BL/6N-Ncoa2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492971	M	MP:0000689	abnormal spleen morphology	Ncoa2<em1(IMPC)Mbp>/Ncoa2<+>	C57BL/6N-Ncoa2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492972	F	MP:0003385	abnormal body wall morphology	Ncoa2<em1(IMPC)Mbp>/Ncoa2<em1(IMPC)Mbp>	C57BL/6N-Ncoa2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492973	M	MP:0001614	abnormal blood vessel morphology	Ncor2<em1(IMPC)Mbp>/Ncor2<em1(IMPC)Mbp>	C57BL/6N-Ncor2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492973	F	MP:0000428	abnormal craniofacial morphology	Ncor2<em1(IMPC)Mbp>/Ncor2<em1(IMPC)Mbp>	C57BL/6N-Ncor2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492976	M	MP:0002941	increased circulating alanine transaminase level	Nefh<tm1.1(KOMP)Vlcg>/Nefh<tm1.1(KOMP)Vlcg>	C57BL/6N-Nefh<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6492976	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Nefh<tm1.1(KOMP)Vlcg>/Nefh<tm1.1(KOMP)Vlcg>	C57BL/6N-Nefh<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6492977	M	MP:0001925	male infertility	Nexmif<em1(IMPC)Tcp>/Nexmif<em1(IMPC)Tcp>	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492979	M	MP:0000691	enlarged spleen	Nhsl2<em1(IMPC)Tcp>/Y	C57BL/6N-Nhsl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492979	M	MP:0011874	enlarged urinary bladder	Nhsl2<em1(IMPC)Tcp>/Y	C57BL/6N-Nhsl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492979	M	MP:0000702	enlarged lymph nodes	Nhsl2<em1(IMPC)Tcp>/Y	C57BL/6N-Nhsl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492979	M	MP:0001200	thick skin	Nhsl2<em1(IMPC)Tcp>/Y	C57BL/6N-Nhsl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492980	F	MP:0002060	abnormal skin morphology	Nhsl2<em1(IMPC)Tcp>/Nhsl2<em1(IMPC)Tcp>	C57BL/6N-Nhsl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492980	F	MP:0000689	abnormal spleen morphology	Nhsl2<em1(IMPC)Tcp>/Nhsl2<em1(IMPC)Tcp>	C57BL/6N-Nhsl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492980	F	MP:0002637	small uterus	Nhsl2<em1(IMPC)Tcp>/Nhsl2<em1(IMPC)Tcp>	C57BL/6N-Nhsl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492980	F	MP:0002092	abnormal eye morphology	Nhsl2<em1(IMPC)Tcp>/Nhsl2<em1(IMPC)Tcp>	C57BL/6N-Nhsl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492980	F	MP:0000702	enlarged lymph nodes	Nhsl2<em1(IMPC)Tcp>/Nhsl2<em1(IMPC)Tcp>	C57BL/6N-Nhsl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492982	M	MP:0001392	abnormal locomotor behavior	Nkpd1<em1(IMPC)J>/Nkpd1<em1(IMPC)J>	C57BL/6NJ-Nkpd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492982	M	MP:0010052	increased grip strength	Nkpd1<em1(IMPC)J>/Nkpd1<em1(IMPC)J>	C57BL/6NJ-Nkpd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492982	M	MP:0010124	decreased bone mineral content	Nkpd1<em1(IMPC)J>/Nkpd1<em1(IMPC)J>	C57BL/6NJ-Nkpd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492984	M	MP:0002997	enlarged seminal vesicle	Nol3<em1(IMPC)Mbp>/Nol3<em1(IMPC)Mbp>	C57BL/6N-Nol3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492984	F	MP:0004832	enlarged ovary	Nol3<em1(IMPC)Mbp>/Nol3<em1(IMPC)Mbp>	C57BL/6N-Nol3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492984	F	MP:0001126	abnormal ovary morphology	Nol3<em1(IMPC)Mbp>/Nol3<em1(IMPC)Mbp>	C57BL/6N-Nol3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492984	M	MP:0000692	small spleen	Nol3<em1(IMPC)Mbp>/Nol3<em1(IMPC)Mbp>	C57BL/6N-Nol3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492984	M	MP:0002989	small kidney	Nol3<em1(IMPC)Mbp>/Nol3<em1(IMPC)Mbp>	C57BL/6N-Nol3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492984	F	MP:0003068	enlarged kidney	Nol3<em1(IMPC)Mbp>/Nol3<em1(IMPC)Mbp>	C57BL/6N-Nol3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492987	F	MP:0002875	decreased erythrocyte cell number	Npepps<em1(IMPC)Hmgu>/Npepps<em1(IMPC)Hmgu>	C57BL/6N-Npepps<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6492987	F	MP:0003179	thrombocytopenia	Npepps<em1(IMPC)Hmgu>/Npepps<em1(IMPC)Hmgu>	C57BL/6N-Npepps<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6492987	M	MP:0003960	increased lean body mass	Npepps<em1(IMPC)Hmgu>/Npepps<em1(IMPC)Hmgu>	C57BL/6N-Npepps<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6492987	F	MP:0010124	decreased bone mineral content	Npepps<em1(IMPC)Hmgu>/Npepps<em1(IMPC)Hmgu>	C57BL/6N-Npepps<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6492987	M	MP:0010025	decreased total body fat amount	Npepps<em1(IMPC)Hmgu>/Npepps<em1(IMPC)Hmgu>	C57BL/6N-Npepps<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6492987	F	MP:0030610	absent teeth	Npepps<em1(IMPC)Hmgu>/Npepps<em1(IMPC)Hmgu>	C57BL/6N-Npepps<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6492987	F	MP:0003795	abnormal bone structure	Npepps<em1(IMPC)Hmgu>/Npepps<em1(IMPC)Hmgu>	C57BL/6N-Npepps<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6492989	M	MP:0001147	small testis	Npr3<tm1.1(KOMP)Vlcg>/Npr3<tm1.1(KOMP)Vlcg>	C57BL/6N-Npr3<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6492989	M	MP:0001146	abnormal testis morphology	Npr3<tm1.1(KOMP)Vlcg>/Npr3<tm1.1(KOMP)Vlcg>	C57BL/6N-Npr3<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:6492990	F	MP:0010052	increased grip strength	Nsl1<em1(IMPC)J>/Nsl1<+>	C57BL/6NJ-Nsl1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492992	M	MP:0010097	abnormal retina blood vessel morphology	Nudt13<tm2b(EUCOMM)Hmgu>/Nudt13<tm2b(EUCOMM)Hmgu>	C57BL/6N-Nudt13<tm2b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6492992	F	MP:0011965	decreased total retina thickness	Nudt13<tm2b(EUCOMM)Hmgu>/Nudt13<tm2b(EUCOMM)Hmgu>	C57BL/6N-Nudt13<tm2b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6492993	M	MP:0010024	increased total body fat amount	Nup205<em1(IMPC)J>/Nup205<+>	C57BL/6NJ-Nup205<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492993	M	MP:0005178	increased circulating cholesterol level	Nup205<em1(IMPC)J>/Nup205<+>	C57BL/6NJ-Nup205<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492993	M	MP:0003961	decreased lean body mass	Nup205<em1(IMPC)J>/Nup205<+>	C57BL/6NJ-Nup205<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492995	M	MP:0005343	increased circulating aspartate transaminase level	Ociad2<em1(IMPC)Tcp>/Ociad2<em1(IMPC)Tcp>	C57BL/6N-Ociad2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492995	M	MP:0002941	increased circulating alanine transaminase level	Ociad2<em1(IMPC)Tcp>/Ociad2<em1(IMPC)Tcp>	C57BL/6N-Ociad2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492995	F	MP:0002968	increased circulating alkaline phosphatase level	Ociad2<em1(IMPC)Tcp>/Ociad2<em1(IMPC)Tcp>	C57BL/6N-Ociad2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6492996	M	MP:0000274	enlarged heart	Otol1<em1(IMPC)Mbp>/Otol1<em1(IMPC)Mbp>	C57BL/6N-Otol1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492996	F	MP:0009709	hydrometra	Otol1<em1(IMPC)Mbp>/Otol1<em1(IMPC)Mbp>	C57BL/6N-Otol1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492996	F	MP:0001120	abnormal uterus morphology	Otol1<em1(IMPC)Mbp>/Otol1<em1(IMPC)Mbp>	C57BL/6N-Otol1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492996	M	MP:0000266	abnormal heart morphology	Otol1<em1(IMPC)Mbp>/Otol1<em1(IMPC)Mbp>	C57BL/6N-Otol1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492998	F	MP:0005333	decreased heart rate	P4ha3<em1(IMPC)J>/P4ha3<em1(IMPC)J>	C57BL/6NJ-P4ha3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492998	M	MP:0001510	abnormal coat appearance	P4ha3<em1(IMPC)J>/P4ha3<em1(IMPC)J>	C57BL/6NJ-P4ha3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6492999	F	MP:0002060	abnormal skin morphology	Pabpc5<em1(IMPC)Mbp>/Pabpc5<em1(IMPC)Mbp>	C57BL/6N-Pabpc5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6492999	F	MP:0002092	abnormal eye morphology	Pabpc5<em1(IMPC)Mbp>/Pabpc5<em1(IMPC)Mbp>	C57BL/6N-Pabpc5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493001	M	MP:0005562	decreased mean corpuscular hemoglobin	Pan3<em1(IMPC)Tcp>/Pan3<+>	C57BL/6N-Pan3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493001	M	MP:0000702	enlarged lymph nodes	Pan3<em1(IMPC)Tcp>/Pan3<+>	C57BL/6N-Pan3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493001	M	MP:0000157	abnormal sternum morphology	Pan3<em1(IMPC)Tcp>/Pan3<+>	C57BL/6N-Pan3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493001	M	MP:0009476	enlarged cecum	Pan3<em1(IMPC)Tcp>/Pan3<+>	C57BL/6N-Pan3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493001	M	MP:0002060	abnormal skin morphology	Pan3<em1(IMPC)Tcp>/Pan3<+>	C57BL/6N-Pan3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493002	M	MP:0000157	abnormal sternum morphology	Pan3<em1(IMPC)Tcp>/Pan3<em1(IMPC)Tcp>	C57BL/6N-Pan3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493003	M	MP:0001402	decreased locomotor activity	Papolg<em1(IMPC)J>/Papolg<+>	C57BL/6NJ-Papolg<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493003	M	MP:0010052	increased grip strength	Papolg<em1(IMPC)J>/Papolg<+>	C57BL/6NJ-Papolg<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493003	F	MP:0005553	increased circulating creatinine level	Papolg<em1(IMPC)J>/Papolg<+>	C57BL/6NJ-Papolg<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493005	F	MP:0000432	abnormal head morphology	Park7<em1(IMPC)H>/Park7<em1(IMPC)H>	C57BL/6NTac-Park7<em1(IMPC)H>/H	N	MGI:5576271
MGI:6493006	F	MP:0000111	cleft palate	Pax6<em1(IMPC)Mbp>/Pax6<em1(IMPC)Mbp>	C57BL/6N-Pax6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493007	M	MP:0011874	enlarged urinary bladder	Pcdhb13<em1(IMPC)Tcp>/Pcdhb13<em1(IMPC)Tcp>	C57BL/6N-Pcdhb13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493007	F	MP:0000157	abnormal sternum morphology	Pcdhb13<em1(IMPC)Tcp>/Pcdhb13<em1(IMPC)Tcp>	C57BL/6N-Pcdhb13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493007	M	MP:0002607	decreased basophil cell number	Pcdhb13<em1(IMPC)Tcp>/Pcdhb13<em1(IMPC)Tcp>	C57BL/6N-Pcdhb13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493007	M	MP:0005179	decreased circulating cholesterol level	Pcdhb13<em1(IMPC)Tcp>/Pcdhb13<em1(IMPC)Tcp>	C57BL/6N-Pcdhb13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493007	M	MP:0000702	enlarged lymph nodes	Pcdhb13<em1(IMPC)Tcp>/Pcdhb13<em1(IMPC)Tcp>	C57BL/6N-Pcdhb13<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493008	M	MP:0010392	prolonged QRS complex duration	Pcdhb9<em1(IMPC)J>/Pcdhb9<em1(IMPC)J>	C57BL/6NJ-Pcdhb9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493008	F	MP:0010097	abnormal retina blood vessel morphology	Pcdhb9<em1(IMPC)J>/Pcdhb9<em1(IMPC)J>	C57BL/6NJ-Pcdhb9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493008	M	MP:0010052	increased grip strength	Pcdhb9<em1(IMPC)J>/Pcdhb9<em1(IMPC)J>	C57BL/6NJ-Pcdhb9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493010	M	MP:0005565	increased blood urea nitrogen level	Pdcd6ip<em1(IMPC)Hmgu>/Pdcd6ip<em1(IMPC)Hmgu>	C57BL/6N-Pdcd6ip<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6493010	M	MP:0000702	enlarged lymph nodes	Pdcd6ip<em1(IMPC)Hmgu>/Pdcd6ip<em1(IMPC)Hmgu>	C57BL/6N-Pdcd6ip<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6493010	M	MP:0010052	increased grip strength	Pdcd6ip<em1(IMPC)Hmgu>/Pdcd6ip<em1(IMPC)Hmgu>	C57BL/6N-Pdcd6ip<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6493011	M	MP:0001146	abnormal testis morphology	Pde11a<em1(IMPC)Mbp>/Pde11a<em1(IMPC)Mbp>	C57BL/6N-Pde11a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493011	F	MP:0002092	abnormal eye morphology	Pde11a<em1(IMPC)Mbp>/Pde11a<em1(IMPC)Mbp>	C57BL/6N-Pde11a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493011	F	MP:0009709	hydrometra	Pde11a<em1(IMPC)Mbp>/Pde11a<em1(IMPC)Mbp>	C57BL/6N-Pde11a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493011	M	MP:0002574	increased vertical activity	Pde11a<em1(IMPC)Mbp>/Pde11a<em1(IMPC)Mbp>	C57BL/6N-Pde11a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493011	F	MP:0001126	abnormal ovary morphology	Pde11a<em1(IMPC)Mbp>/Pde11a<em1(IMPC)Mbp>	C57BL/6N-Pde11a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493011	F	MP:0001120	abnormal uterus morphology	Pde11a<em1(IMPC)Mbp>/Pde11a<em1(IMPC)Mbp>	C57BL/6N-Pde11a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493011	M	MP:0001147	small testis	Pde11a<em1(IMPC)Mbp>/Pde11a<em1(IMPC)Mbp>	C57BL/6N-Pde11a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493011	F	MP:0001297	microphthalmia	Pde11a<em1(IMPC)Mbp>/Pde11a<em1(IMPC)Mbp>	C57BL/6N-Pde11a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493012	F	MP:0001258	decreased body length	Pde5a<em1(IMPC)Mbp>/Pde5a<+>	C57BL/6N-Pde5a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493012	M	MP:0000689	abnormal spleen morphology	Pde5a<em1(IMPC)Mbp>/Pde5a<+>	C57BL/6N-Pde5a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493012	F	MP:0000601	small liver	Pde5a<em1(IMPC)Mbp>/Pde5a<+>	C57BL/6N-Pde5a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493012	F	MP:0000598	abnormal liver morphology	Pde5a<em1(IMPC)Mbp>/Pde5a<+>	C57BL/6N-Pde5a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493012	M	MP:0000691	enlarged spleen	Pde5a<em1(IMPC)Mbp>/Pde5a<+>	C57BL/6N-Pde5a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493013	M	MP:0000266	abnormal heart morphology	Pde6a<em1(IMPC)Mbp>/Pde6a<em1(IMPC)Mbp>	C57BL/6NCrl-Pde6a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493013	F	MP:0002092	abnormal eye morphology	Pde6a<em1(IMPC)Mbp>/Pde6a<em1(IMPC)Mbp>	C57BL/6NCrl-Pde6a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493013	F	MP:0001566	increased circulating phosphate level	Pde6a<em1(IMPC)Mbp>/Pde6a<em1(IMPC)Mbp>	C57BL/6NCrl-Pde6a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493013	M	MP:0000274	enlarged heart	Pde6a<em1(IMPC)Mbp>/Pde6a<em1(IMPC)Mbp>	C57BL/6NCrl-Pde6a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493014	M	MP:0000538	abnormal urinary bladder morphology	Pdgfd<em1(IMPC)Ccpcz>/Pdgfd<em1(IMPC)Ccpcz>	C57BL/6N-Pdgfd<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493014	M	MP:0005628	decreased circulating potassium level	Pdgfd<em1(IMPC)Ccpcz>/Pdgfd<em1(IMPC)Ccpcz>	C57BL/6N-Pdgfd<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493014	M	MP:0002135	abnormal kidney morphology	Pdgfd<em1(IMPC)Ccpcz>/Pdgfd<em1(IMPC)Ccpcz>	C57BL/6N-Pdgfd<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493020	M	MP:0001488	increased startle reflex	Phlpp2<em1(IMPC)H>/Phlpp2<em1(IMPC)H>	C57BL/6NTac-Phlpp2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6493021	M	MP:0005016	decreased lymphocyte cell number	Phyh<tm1b(EUCOMM)Wtsi>/Phyh<tm1b(EUCOMM)Wtsi>	C57BL/6N-Phyh<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6493021	M	MP:0000219	increased neutrophil cell number	Phyh<tm1b(EUCOMM)Wtsi>/Phyh<tm1b(EUCOMM)Wtsi>	C57BL/6N-Phyh<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6493025	M	MP:0002092	abnormal eye morphology	Pja1<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Pja1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493025	M	MP:0000598	abnormal liver morphology	Pja1<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Pja1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493025	M	MP:0001304	cataract	Pja1<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Pja1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493025	M	MP:0002060	abnormal skin morphology	Pja1<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Pja1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493025	M	MP:0001297	microphthalmia	Pja1<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Pja1<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493027	F	MP:0001399	hyperactivity	Pla2g2d<tm1.1(KOMP)Vlcg>/Pla2g2d<tm1.1(KOMP)Vlcg>	C57BL/6N-Pla2g2d<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6493030	M	MP:0010052	increased grip strength	Pole3<em1(IMPC)J>/Pole3<+>	C57BL/6NJ-Pole3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493032	M	MP:0000689	abnormal spleen morphology	Polq<em1(IMPC)Mbp>/Polq<em1(IMPC)Mbp>	C57BL/6N-Polq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493032	M	MP:0010052	increased grip strength	Polq<em1(IMPC)Mbp>/Polq<em1(IMPC)Mbp>	C57BL/6N-Polq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493032	M	MP:0000692	small spleen	Polq<em1(IMPC)Mbp>/Polq<em1(IMPC)Mbp>	C57BL/6N-Polq<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493037	F	MP:0001566	increased circulating phosphate level	Ppox<em1(IMPC)J>/Ppox<+>	C57BL/6NJ-Ppox<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493037	F	MP:0002941	increased circulating alanine transaminase level	Ppox<em1(IMPC)J>/Ppox<+>	C57BL/6NJ-Ppox<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493039	M	MP:0001697	abnormal embryo size	Pqbp1<em1(IMPC)Tcp>/Y	C57BL/6N-Pqbp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493040	F	MP:0002092	abnormal eye morphology	Pramel12<em1(IMPC)Mbp>/Pramel12<em1(IMPC)Mbp>	C57BL/6N-Pramel12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493040	M	MP:0004002	abnormal jejunum morphology	Pramel12<em1(IMPC)Mbp>/Pramel12<em1(IMPC)Mbp>	C57BL/6N-Pramel12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493040	M	MP:0002997	enlarged seminal vesicle	Pramel12<em1(IMPC)Mbp>/Pramel12<em1(IMPC)Mbp>	C57BL/6N-Pramel12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493040	M	MP:0001147	small testis	Pramel12<em1(IMPC)Mbp>/Pramel12<em1(IMPC)Mbp>	C57BL/6N-Pramel12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493040	F	MP:0002989	small kidney	Pramel12<em1(IMPC)Mbp>/Pramel12<em1(IMPC)Mbp>	C57BL/6N-Pramel12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493040	M	MP:0000470	abnormal stomach morphology	Pramel12<em1(IMPC)Mbp>/Pramel12<em1(IMPC)Mbp>	C57BL/6N-Pramel12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493040	M	MP:0002059	abnormal seminal vesicle morphology	Pramel12<em1(IMPC)Mbp>/Pramel12<em1(IMPC)Mbp>	C57BL/6N-Pramel12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493040	M	MP:0000538	abnormal urinary bladder morphology	Pramel12<em1(IMPC)Mbp>/Pramel12<em1(IMPC)Mbp>	C57BL/6N-Pramel12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493040	M	MP:0001146	abnormal testis morphology	Pramel12<em1(IMPC)Mbp>/Pramel12<em1(IMPC)Mbp>	C57BL/6N-Pramel12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493040	M	MP:0001925	male infertility	Pramel12<em1(IMPC)Mbp>/Pramel12<em1(IMPC)Mbp>	C57BL/6N-Pramel12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493040	F	MP:0001944	abnormal pancreas morphology	Pramel12<em1(IMPC)Mbp>/Pramel12<em1(IMPC)Mbp>	C57BL/6N-Pramel12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493040	M	MP:0003271	abnormal duodenum morphology	Pramel12<em1(IMPC)Mbp>/Pramel12<em1(IMPC)Mbp>	C57BL/6N-Pramel12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493040	M	MP:0000494	abnormal cecum morphology	Pramel12<em1(IMPC)Mbp>/Pramel12<em1(IMPC)Mbp>	C57BL/6N-Pramel12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493042	M	MP:0005293	impaired glucose tolerance	Prdm8<em1(IMPC)Wtsi>/Prdm8<em1(IMPC)Wtsi>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493042	F	MP:0001325	abnormal retina morphology	Prdm8<em1(IMPC)Wtsi>/Prdm8<em1(IMPC)Wtsi>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493042	F	MP:0020421	increased freezing behavior	Prdm8<em1(IMPC)Wtsi>/Prdm8<em1(IMPC)Wtsi>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493042	M	MP:0001399	hyperactivity	Prdm8<em1(IMPC)Wtsi>/Prdm8<em1(IMPC)Wtsi>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493042	F	MP:0000703	abnormal thymus morphology	Prdm8<em1(IMPC)Wtsi>/Prdm8<em1(IMPC)Wtsi>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493042	F	MP:0002188	small heart	Prdm8<em1(IMPC)Wtsi>/Prdm8<em1(IMPC)Wtsi>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493042	F	MP:0001120	abnormal uterus morphology	Prdm8<em1(IMPC)Wtsi>/Prdm8<em1(IMPC)Wtsi>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493042	M	MP:0001262	decreased body weight	Prdm8<em1(IMPC)Wtsi>/Prdm8<em1(IMPC)Wtsi>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493042	F	MP:0000266	abnormal heart morphology	Prdm8<em1(IMPC)Wtsi>/Prdm8<em1(IMPC)Wtsi>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493042	F	MP:0005633	increased circulating sodium level	Prdm8<em1(IMPC)Wtsi>/Prdm8<em1(IMPC)Wtsi>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493042	F	MP:0000709	enlarged thymus	Prdm8<em1(IMPC)Wtsi>/Prdm8<em1(IMPC)Wtsi>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493042	F	MP:0004906	enlarged uterus	Prdm8<em1(IMPC)Wtsi>/Prdm8<em1(IMPC)Wtsi>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493045	M	MP:0001262	decreased body weight	Prss12<em1(IMPC)Ccpcz>/Prss12<em1(IMPC)Ccpcz>	C57BL/6N-Prss12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493045	F	MP:0000703	abnormal thymus morphology	Prss12<em1(IMPC)Ccpcz>/Prss12<em1(IMPC)Ccpcz>	C57BL/6N-Prss12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493045	M	MP:0011971	increased circulating lactate dehydrogenase level	Prss12<em1(IMPC)Ccpcz>/Prss12<em1(IMPC)Ccpcz>	C57BL/6N-Prss12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493045	F	MP:0002092	abnormal eye morphology	Prss12<em1(IMPC)Ccpcz>/Prss12<em1(IMPC)Ccpcz>	C57BL/6N-Prss12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493045	F	MP:0000709	enlarged thymus	Prss12<em1(IMPC)Ccpcz>/Prss12<em1(IMPC)Ccpcz>	C57BL/6N-Prss12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493046	M	MP:0013519	decreased CD4-positive NK T cell number	Prss54<em1(IMPC)Ccpcz>/Prss54<em1(IMPC)Ccpcz>	C57BL/6N-Prss54<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493046	F	MP:0000160	kyphosis	Prss54<em1(IMPC)Ccpcz>/Prss54<em1(IMPC)Ccpcz>	C57BL/6N-Prss54<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493046	F	MP:0004174	abnormal spine curvature	Prss54<em1(IMPC)Ccpcz>/Prss54<em1(IMPC)Ccpcz>	C57BL/6N-Prss54<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493046	M	MP:0001489	decreased startle reflex	Prss54<em1(IMPC)Ccpcz>/Prss54<em1(IMPC)Ccpcz>	C57BL/6N-Prss54<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493046	F	MP:0000703	abnormal thymus morphology	Prss54<em1(IMPC)Ccpcz>/Prss54<em1(IMPC)Ccpcz>	C57BL/6N-Prss54<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493046	M	MP:0008040	decreased NK T cell number	Prss54<em1(IMPC)Ccpcz>/Prss54<em1(IMPC)Ccpcz>	C57BL/6N-Prss54<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493046	M	MP:0002060	abnormal skin morphology	Prss54<em1(IMPC)Ccpcz>/Prss54<em1(IMPC)Ccpcz>	C57BL/6N-Prss54<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493046	M	MP:0013522	decreased memory-marker CD4-positive NK T cell number	Prss54<em1(IMPC)Ccpcz>/Prss54<em1(IMPC)Ccpcz>	C57BL/6N-Prss54<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493046	M	MP:0000266	abnormal heart morphology	Prss54<em1(IMPC)Ccpcz>/Prss54<em1(IMPC)Ccpcz>	C57BL/6N-Prss54<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493046	F	MP:0000709	enlarged thymus	Prss54<em1(IMPC)Ccpcz>/Prss54<em1(IMPC)Ccpcz>	C57BL/6N-Prss54<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493046	M	MP:0000274	enlarged heart	Prss54<em1(IMPC)Ccpcz>/Prss54<em1(IMPC)Ccpcz>	C57BL/6N-Prss54<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493049	F	MP:0004258	abnormal placenta size	Pus7<em1(IMPC)J>/Pus7<em1(IMPC)J>	C57BL/6NJ-Pus7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493050	M	MP:0002079	increased circulating insulin level	Pvr<em1(IMPC)Wtsi>/Pvr<em1(IMPC)Wtsi>	C57BL/6N-Pvr<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493052	F	MP:0010124	decreased bone mineral content	Qrsl1<em1(IMPC)J>/Qrsl1<+>	C57BL/6NJ-Qrsl1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493059	M	MP:0001392	abnormal locomotor behavior	Retreg1<em1(IMPC)J>/Retreg1<em1(IMPC)J>	C57BL/6NJ-Retreg1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493059	M	MP:0001417	decreased exploration in new environment	Retreg1<em1(IMPC)J>/Retreg1<em1(IMPC)J>	C57BL/6NJ-Retreg1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493060	M	MP:0000691	enlarged spleen	Rffl<em1(IMPC)Ccpcz>/Rffl<em1(IMPC)Ccpcz>	C57BL/6N-Rffl<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493060	M	MP:0000689	abnormal spleen morphology	Rffl<em1(IMPC)Ccpcz>/Rffl<em1(IMPC)Ccpcz>	C57BL/6N-Rffl<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493060	M	MP:0000266	abnormal heart morphology	Rffl<em1(IMPC)Ccpcz>/Rffl<em1(IMPC)Ccpcz>	C57BL/6N-Rffl<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493060	M	MP:0000277	abnormal heart shape	Rffl<em1(IMPC)Ccpcz>/Rffl<em1(IMPC)Ccpcz>	C57BL/6N-Rffl<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493061	M	MP:0001944	abnormal pancreas morphology	Rgcc<tm1.1(KOMP)Wtsi>/Rgcc<tm1.1(KOMP)Wtsi>	C57BL/6N-Rgcc<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6493061	M	MP:0000266	abnormal heart morphology	Rgcc<tm1.1(KOMP)Wtsi>/Rgcc<tm1.1(KOMP)Wtsi>	C57BL/6N-Rgcc<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6493061	M	MP:0000274	enlarged heart	Rgcc<tm1.1(KOMP)Wtsi>/Rgcc<tm1.1(KOMP)Wtsi>	C57BL/6N-Rgcc<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6493061	M	MP:0004931	enlarged epididymis	Rgcc<tm1.1(KOMP)Wtsi>/Rgcc<tm1.1(KOMP)Wtsi>	C57BL/6N-Rgcc<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6493061	M	MP:0002631	abnormal epididymis morphology	Rgcc<tm1.1(KOMP)Wtsi>/Rgcc<tm1.1(KOMP)Wtsi>	C57BL/6N-Rgcc<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6493062	M	MP:0001510	abnormal coat appearance	Rhbdf2<em1(IMPC)Wtsi>/Rhbdf2<+>	C57BL/6N-Rhbdf2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493062	M	MP:0002098	abnormal vibrissa morphology	Rhbdf2<em1(IMPC)Wtsi>/Rhbdf2<+>	C57BL/6N-Rhbdf2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493063	M	MP:0010092	increased circulating magnesium level	Rhbdf2<em1(IMPC)Wtsi>/Rhbdf2<em1(IMPC)Wtsi>	C57BL/6N-Rhbdf2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493063	M	MP:0002073	abnormal hair growth	Rhbdf2<em1(IMPC)Wtsi>/Rhbdf2<em1(IMPC)Wtsi>	C57BL/6N-Rhbdf2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493063	M	MP:0005561	increased mean corpuscular hemoglobin	Rhbdf2<em1(IMPC)Wtsi>/Rhbdf2<em1(IMPC)Wtsi>	C57BL/6N-Rhbdf2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493064	F	MP:0000470	abnormal stomach morphology	Rnase6<em1(IMPC)Tcp>/Rnase6<em1(IMPC)Tcp>	C57BL/6N-Rnase6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493064	F	MP:0001126	abnormal ovary morphology	Rnase6<em1(IMPC)Tcp>/Rnase6<em1(IMPC)Tcp>	C57BL/6N-Rnase6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493064	M	MP:0000157	abnormal sternum morphology	Rnase6<em1(IMPC)Tcp>/Rnase6<em1(IMPC)Tcp>	C57BL/6N-Rnase6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493065	F	MP:0000157	abnormal sternum morphology	Rnf113a1<em1(IMPC)Tcp>/Rnf113a1<em1(IMPC)Tcp>	C57BL/6N-Rnf113a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493066	M	MP:0001399	hyperactivity	Rnf123<em1(IMPC)J>/Rnf123<em1(IMPC)J>	C57BL/6NJ-Rnf123<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493066	F	MP:0005292	improved glucose tolerance	Rnf123<em1(IMPC)J>/Rnf123<em1(IMPC)J>	C57BL/6NJ-Rnf123<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493067	F	MP:0001402	decreased locomotor activity	Rnf148<em1(IMPC)Ccpcz>/Rnf148<em1(IMPC)Ccpcz>	C57BL/6N-Rnf148<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493067	F	MP:0000703	abnormal thymus morphology	Rnf148<em1(IMPC)Ccpcz>/Rnf148<em1(IMPC)Ccpcz>	C57BL/6N-Rnf148<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493067	M	MP:0002286	cryptorchism	Rnf148<em1(IMPC)Ccpcz>/Rnf148<em1(IMPC)Ccpcz>	C57BL/6N-Rnf148<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493067	F	MP:0000709	enlarged thymus	Rnf148<em1(IMPC)Ccpcz>/Rnf148<em1(IMPC)Ccpcz>	C57BL/6N-Rnf148<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493067	F	MP:0004924	abnormal behavior	Rnf148<em1(IMPC)Ccpcz>/Rnf148<em1(IMPC)Ccpcz>	C57BL/6N-Rnf148<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493067	M	MP:0000160	kyphosis	Rnf148<em1(IMPC)Ccpcz>/Rnf148<em1(IMPC)Ccpcz>	C57BL/6N-Rnf148<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493067	M	MP:0001146	abnormal testis morphology	Rnf148<em1(IMPC)Ccpcz>/Rnf148<em1(IMPC)Ccpcz>	C57BL/6N-Rnf148<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493067	F	MP:0020870	decreased thigmotaxis	Rnf148<em1(IMPC)Ccpcz>/Rnf148<em1(IMPC)Ccpcz>	C57BL/6N-Rnf148<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493067	M	MP:0005419	decreased circulating serum albumin level	Rnf148<em1(IMPC)Ccpcz>/Rnf148<em1(IMPC)Ccpcz>	C57BL/6N-Rnf148<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493067	F	MP:0001399	hyperactivity	Rnf148<em1(IMPC)Ccpcz>/Rnf148<em1(IMPC)Ccpcz>	C57BL/6N-Rnf148<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493067	M	MP:0004174	abnormal spine curvature	Rnf148<em1(IMPC)Ccpcz>/Rnf148<em1(IMPC)Ccpcz>	C57BL/6N-Rnf148<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493069	M	MP:0003604	single kidney	Rnf223<em1(IMPC)Ccpcz>/Rnf223<em1(IMPC)Ccpcz>	C57BL/6N-Rnf223<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493069	F	MP:0000703	abnormal thymus morphology	Rnf223<em1(IMPC)Ccpcz>/Rnf223<em1(IMPC)Ccpcz>	C57BL/6N-Rnf223<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493069	F	MP:0000691	enlarged spleen	Rnf223<em1(IMPC)Ccpcz>/Rnf223<em1(IMPC)Ccpcz>	C57BL/6N-Rnf223<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493069	M	MP:0002339	abnormal lymph node morphology	Rnf223<em1(IMPC)Ccpcz>/Rnf223<em1(IMPC)Ccpcz>	C57BL/6N-Rnf223<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493069	F	MP:0000709	enlarged thymus	Rnf223<em1(IMPC)Ccpcz>/Rnf223<em1(IMPC)Ccpcz>	C57BL/6N-Rnf223<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493069	M	MP:0000274	enlarged heart	Rnf223<em1(IMPC)Ccpcz>/Rnf223<em1(IMPC)Ccpcz>	C57BL/6N-Rnf223<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493069	F	MP:0000689	abnormal spleen morphology	Rnf223<em1(IMPC)Ccpcz>/Rnf223<em1(IMPC)Ccpcz>	C57BL/6N-Rnf223<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493069	M	MP:0000702	enlarged lymph nodes	Rnf223<em1(IMPC)Ccpcz>/Rnf223<em1(IMPC)Ccpcz>	C57BL/6N-Rnf223<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493069	M	MP:0000266	abnormal heart morphology	Rnf223<em1(IMPC)Ccpcz>/Rnf223<em1(IMPC)Ccpcz>	C57BL/6N-Rnf223<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493069	M	MP:0002135	abnormal kidney morphology	Rnf223<em1(IMPC)Ccpcz>/Rnf223<em1(IMPC)Ccpcz>	C57BL/6N-Rnf223<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493070	F	MP:0001417	decreased exploration in new environment	Rnf44<em1(IMPC)Bay>/Rnf44<em1(IMPC)Bay>	C57BL/6N-Rnf44<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6493071	F	MP:0000562	polydactyly	Ror2<em1(IMPC)Mbp>/Ror2<em1(IMPC)Mbp>	C57BL/6N-Ror2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493073	M	MP:0003960	increased lean body mass	Rrbp1<em1(IMPC)J>/Rrbp1<em1(IMPC)J>	C57BL/6NJ-Rrbp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493073	M	MP:0005419	decreased circulating serum albumin level	Rrbp1<em1(IMPC)J>/Rrbp1<em1(IMPC)J>	C57BL/6NJ-Rrbp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493073	M	MP:0005635	decreased circulating bilirubin level	Rrbp1<em1(IMPC)J>/Rrbp1<em1(IMPC)J>	C57BL/6NJ-Rrbp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493073	M	MP:0005562	decreased mean corpuscular hemoglobin	Rrbp1<em1(IMPC)J>/Rrbp1<em1(IMPC)J>	C57BL/6NJ-Rrbp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493073	M	MP:0005567	decreased circulating total protein level	Rrbp1<em1(IMPC)J>/Rrbp1<em1(IMPC)J>	C57BL/6NJ-Rrbp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493073	M	MP:0005278	abnormal cholesterol homeostasis	Rrbp1<em1(IMPC)J>/Rrbp1<em1(IMPC)J>	C57BL/6NJ-Rrbp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493073	M	MP:0010124	decreased bone mineral content	Rrbp1<em1(IMPC)J>/Rrbp1<em1(IMPC)J>	C57BL/6NJ-Rrbp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493073	M	MP:0001304	cataract	Rrbp1<em1(IMPC)J>/Rrbp1<em1(IMPC)J>	C57BL/6NJ-Rrbp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493073	M	MP:0002591	decreased mean corpuscular volume	Rrbp1<em1(IMPC)J>/Rrbp1<em1(IMPC)J>	C57BL/6NJ-Rrbp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493073	M	MP:0002644	decreased circulating triglyceride level	Rrbp1<em1(IMPC)J>/Rrbp1<em1(IMPC)J>	C57BL/6NJ-Rrbp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493074	M	MP:0005655	increased aggression	Rtl3<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Rtl3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493074	M	MP:0020421	increased freezing behavior	Rtl3<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Rtl3<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493075	M	MP:0000266	abnormal heart morphology	Rtl5<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Rtl5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493075	M	MP:0002092	abnormal eye morphology	Rtl5<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Rtl5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493075	M	MP:0003068	enlarged kidney	Rtl5<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Rtl5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493075	M	MP:0020421	increased freezing behavior	Rtl5<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Rtl5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493075	M	MP:0002135	abnormal kidney morphology	Rtl5<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Rtl5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493075	M	MP:0000274	enlarged heart	Rtl5<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Rtl5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493075	M	MP:0001297	microphthalmia	Rtl5<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Rtl5<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493076	M	MP:0003961	decreased lean body mass	Rufy1<em1(IMPC)J>/Rufy1<em1(IMPC)J>	C57BL/6N-Rufy1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6493079	F	MP:0002968	increased circulating alkaline phosphatase level	Scfd2<em1(IMPC)J>/Scfd2<em1(IMPC)J>	C57BL/6NJ-Scfd2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493084	M	MP:0002941	increased circulating alanine transaminase level	Sel1l3<em1(IMPC)J>/Sel1l3<em1(IMPC)J>	C57BL/6NJ-Sel1l3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493084	M	MP:0010052	increased grip strength	Sel1l3<em1(IMPC)J>/Sel1l3<em1(IMPC)J>	C57BL/6NJ-Sel1l3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493087	M	MP:0005293	impaired glucose tolerance	Serinc2<em1(IMPC)J>/Serinc2<em1(IMPC)J>	C57BL/6NJ-Serinc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493088	F	MP:0005568	increased circulating total protein level	Serpina1f<em1(IMPC)J>/Serpina1f<em1(IMPC)J>	C57BL/6NJ-Serpina1f<em1(IMPC)J>/J	N	MGI:5576271
MGI:6493091	F	MP:0002339	abnormal lymph node morphology	Sfmbt2<em1(IMPC)Mbp>/Sfmbt2<+>	C57BL/6NCrl-Sfmbt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493091	M	MP:0003068	enlarged kidney	Sfmbt2<em1(IMPC)Mbp>/Sfmbt2<+>	C57BL/6NCrl-Sfmbt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493091	M	MP:0002135	abnormal kidney morphology	Sfmbt2<em1(IMPC)Mbp>/Sfmbt2<+>	C57BL/6NCrl-Sfmbt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493091	F	MP:0000598	abnormal liver morphology	Sfmbt2<em1(IMPC)Mbp>/Sfmbt2<+>	C57BL/6NCrl-Sfmbt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493091	F	MP:0000702	enlarged lymph nodes	Sfmbt2<em1(IMPC)Mbp>/Sfmbt2<+>	C57BL/6NCrl-Sfmbt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493091	M	MP:0020421	increased freezing behavior	Sfmbt2<em1(IMPC)Mbp>/Sfmbt2<+>	C57BL/6NCrl-Sfmbt2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493094	F	MP:0004832	enlarged ovary	Shank1<em1(IMPC)Mbp>/Shank1<em1(IMPC)Mbp>	C57BL/6N-Shank1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493094	F	MP:0002699	abnormal vitreous body morphology	Shank1<em1(IMPC)Mbp>/Shank1<em1(IMPC)Mbp>	C57BL/6N-Shank1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493094	M	MP:0000367	abnormal coat/ hair morphology	Shank1<em1(IMPC)Mbp>/Shank1<em1(IMPC)Mbp>	C57BL/6N-Shank1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493094	F	MP:0000598	abnormal liver morphology	Shank1<em1(IMPC)Mbp>/Shank1<em1(IMPC)Mbp>	C57BL/6N-Shank1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493094	F	MP:0009342	enlarged gallbladder	Shank1<em1(IMPC)Mbp>/Shank1<em1(IMPC)Mbp>	C57BL/6N-Shank1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493094	M	MP:0001406	abnormal gait	Shank1<em1(IMPC)Mbp>/Shank1<em1(IMPC)Mbp>	C57BL/6N-Shank1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493094	F	MP:0001126	abnormal ovary morphology	Shank1<em1(IMPC)Mbp>/Shank1<em1(IMPC)Mbp>	C57BL/6N-Shank1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493094	F	MP:0005084	abnormal gallbladder morphology	Shank1<em1(IMPC)Mbp>/Shank1<em1(IMPC)Mbp>	C57BL/6N-Shank1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493094	F	MP:0000601	small liver	Shank1<em1(IMPC)Mbp>/Shank1<em1(IMPC)Mbp>	C57BL/6N-Shank1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493094	F	MP:0010052	increased grip strength	Shank1<em1(IMPC)Mbp>/Shank1<em1(IMPC)Mbp>	C57BL/6N-Shank1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493095	M	MP:0010067	increased red blood cell distribution width	Shld1<em1(IMPC)Wtsi>/Shld1<em1(IMPC)Wtsi>	C57BL/6N-Shld1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493096	M	MP:0001325	abnormal retina morphology	Shroom2<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Shroom2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493096	M	MP:0002968	increased circulating alkaline phosphatase level	Shroom2<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Shroom2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493097	M	MP:0004151	decreased circulating iron level	Sidt2<em1(IMPC)Wtsi>/Sidt2<em1(IMPC)Wtsi>	C57BL/6N-Sidt2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493097	M	MP:0003442	decreased circulating glycerol level	Sidt2<em1(IMPC)Wtsi>/Sidt2<em1(IMPC)Wtsi>	C57BL/6N-Sidt2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493097	M	MP:0000183	decreased circulating LDL cholesterol level	Sidt2<em1(IMPC)Wtsi>/Sidt2<em1(IMPC)Wtsi>	C57BL/6N-Sidt2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493097	M	MP:0005179	decreased circulating cholesterol level	Sidt2<em1(IMPC)Wtsi>/Sidt2<em1(IMPC)Wtsi>	C57BL/6N-Sidt2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493097	M	MP:0000186	decreased circulating HDL cholesterol level	Sidt2<em1(IMPC)Wtsi>/Sidt2<em1(IMPC)Wtsi>	C57BL/6N-Sidt2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493097	M	MP:0005505	thrombocytosis	Sidt2<em1(IMPC)Wtsi>/Sidt2<em1(IMPC)Wtsi>	C57BL/6N-Sidt2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493098	F	MP:0000438	abnormal cranium morphology	Sla2<em1(IMPC)Ccpcz>/Sla2<em1(IMPC)Ccpcz>	C57BL/6N-Sla2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493098	M	MP:0001262	decreased body weight	Sla2<em1(IMPC)Ccpcz>/Sla2<em1(IMPC)Ccpcz>	C57BL/6N-Sla2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493098	M	MP:0005568	increased circulating total protein level	Sla2<em1(IMPC)Ccpcz>/Sla2<em1(IMPC)Ccpcz>	C57BL/6N-Sla2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493098	M	MP:0002060	abnormal skin morphology	Sla2<em1(IMPC)Ccpcz>/Sla2<em1(IMPC)Ccpcz>	C57BL/6N-Sla2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493102	F	MP:0010053	decreased grip strength	Slc17a2<em1(IMPC)J>/Slc17a2<em1(IMPC)J>	C57BL/6NJ-Slc17a2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493103	F	MP:0000691	enlarged spleen	Slc22a29<em1(IMPC)Mbp>/Slc22a29<em1(IMPC)Mbp>	C57BL/6N-Slc22a29<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493103	F	MP:0000689	abnormal spleen morphology	Slc22a29<em1(IMPC)Mbp>/Slc22a29<em1(IMPC)Mbp>	C57BL/6N-Slc22a29<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493105	M	MP:0011874	enlarged urinary bladder	Slc36a1<em1(IMPC)Tcp>/Slc36a1<+>	C57BL/6N-Slc36a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493105	M	MP:0002060	abnormal skin morphology	Slc36a1<em1(IMPC)Tcp>/Slc36a1<+>	C57BL/6N-Slc36a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493105	M	MP:0000470	abnormal stomach morphology	Slc36a1<em1(IMPC)Tcp>/Slc36a1<+>	C57BL/6N-Slc36a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493105	M	MP:0000157	abnormal sternum morphology	Slc36a1<em1(IMPC)Tcp>/Slc36a1<+>	C57BL/6N-Slc36a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493107	F	MP:0002098	abnormal vibrissa morphology	Slc4a1ap<em1(IMPC)J>/Slc4a1ap<em1(IMPC)J>	C57BL/6NJ-Slc4a1ap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493107	F	MP:0001417	decreased exploration in new environment	Slc4a1ap<em1(IMPC)J>/Slc4a1ap<em1(IMPC)J>	C57BL/6NJ-Slc4a1ap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493109	F	MP:0001415	increased exploration in new environment	Slc6a7<em1(IMPC)J>/Slc6a7<em1(IMPC)J>	C57BL/6NJ-Slc6a7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493113	M	MP:0001415	increased exploration in new environment	Slitrk2<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Slitrk2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493113	M	MP:0002833	increased heart weight	Slitrk2<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Slitrk2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493113	M	MP:0020870	decreased thigmotaxis	Slitrk2<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Slitrk2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493115	M	MP:0002644	decreased circulating triglyceride level	Snx12<em1(IMPC)J>/Y	C57BL/6NJ-Snx12<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493116	F	MP:0010393	shortened QRS complex duration	Snx12<em1(IMPC)J>/Snx12<em1(IMPC)J>	C57BL/6NJ-Snx12<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493116	F	MP:0010052	increased grip strength	Snx12<em1(IMPC)J>/Snx12<em1(IMPC)J>	C57BL/6NJ-Snx12<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493117	F	MP:0001556	increased circulating HDL cholesterol level	Snx6<em1(IMPC)J>/Snx6<em1(IMPC)J>	C57BL/6NJ-Snx6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493117	F	MP:0005178	increased circulating cholesterol level	Snx6<em1(IMPC)J>/Snx6<em1(IMPC)J>	C57BL/6NJ-Snx6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493117	F	MP:0001402	decreased locomotor activity	Snx6<em1(IMPC)J>/Snx6<em1(IMPC)J>	C57BL/6NJ-Snx6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493119	F	MP:0005561	increased mean corpuscular hemoglobin	Son<em1(IMPC)Wtsi>/Son<em1(IMPC)Wtsi>	C57BL/6N-Son<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493120	M	MP:0002152	abnormal brain morphology	Sox2<em1(IMPC)Mbp>/Sox2<+>	C57BL/6N-Sox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493120	M	MP:0009453	enhanced contextual conditioning behavior	Sox2<em1(IMPC)Mbp>/Sox2<+>	C57BL/6N-Sox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493120	M	MP:0001319	irregularly shaped pupil	Sox2<em1(IMPC)Mbp>/Sox2<+>	C57BL/6N-Sox2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493122	F	MP:0002098	abnormal vibrissa morphology	Spatc1<em1(IMPC)J>/Spatc1<em1(IMPC)J>	C57BL/6NJ-Spatc1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493122	F	MP:0001566	increased circulating phosphate level	Spatc1<em1(IMPC)J>/Spatc1<em1(IMPC)J>	C57BL/6NJ-Spatc1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493123	F	MP:0001284	absent vibrissae	Spink5<em1(IMPC)J>/Spink5<+>	C57BL/6NJ-Spink5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493132	M	MP:0000691	enlarged spleen	Stoml1<em1(IMPC)Tcp>/Stoml1<em1(IMPC)Tcp>	C57BL/6N-Stoml1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493132	M	MP:0002059	abnormal seminal vesicle morphology	Stoml1<em1(IMPC)Tcp>/Stoml1<em1(IMPC)Tcp>	C57BL/6N-Stoml1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493132	M	MP:0000702	enlarged lymph nodes	Stoml1<em1(IMPC)Tcp>/Stoml1<em1(IMPC)Tcp>	C57BL/6N-Stoml1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493132	F	MP:0001944	abnormal pancreas morphology	Stoml1<em1(IMPC)Tcp>/Stoml1<em1(IMPC)Tcp>	C57BL/6N-Stoml1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493132	M	MP:0002092	abnormal eye morphology	Stoml1<em1(IMPC)Tcp>/Stoml1<em1(IMPC)Tcp>	C57BL/6N-Stoml1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493133	F	MP:0001402	decreased locomotor activity	Stt3b<em1(IMPC)J>/Stt3b<+>	C57BL/6NJ-Stt3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493133	M	MP:0002941	increased circulating alanine transaminase level	Stt3b<em1(IMPC)J>/Stt3b<+>	C57BL/6NJ-Stt3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493133	M	MP:0005344	increased circulating bilirubin level	Stt3b<em1(IMPC)J>/Stt3b<+>	C57BL/6NJ-Stt3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493133	M	MP:0005562	decreased mean corpuscular hemoglobin	Stt3b<em1(IMPC)J>/Stt3b<+>	C57BL/6NJ-Stt3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493133	F	MP:0001417	decreased exploration in new environment	Stt3b<em1(IMPC)J>/Stt3b<+>	C57BL/6NJ-Stt3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493136	F	MP:0002092	abnormal eye morphology	Sun5<em1(IMPC)Mbp>/Sun5<em1(IMPC)Mbp>	C57BL/6N-Sun5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493136	M	MP:0001925	male infertility	Sun5<em1(IMPC)Mbp>/Sun5<em1(IMPC)Mbp>	C57BL/6N-Sun5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493136	F	MP:0000691	enlarged spleen	Sun5<em1(IMPC)Mbp>/Sun5<em1(IMPC)Mbp>	C57BL/6N-Sun5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493136	M	MP:0002997	enlarged seminal vesicle	Sun5<em1(IMPC)Mbp>/Sun5<em1(IMPC)Mbp>	C57BL/6N-Sun5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493136	M	MP:0000598	abnormal liver morphology	Sun5<em1(IMPC)Mbp>/Sun5<em1(IMPC)Mbp>	C57BL/6N-Sun5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493136	M	MP:0001148	enlarged testis	Sun5<em1(IMPC)Mbp>/Sun5<em1(IMPC)Mbp>	C57BL/6N-Sun5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493136	M	MP:0001146	abnormal testis morphology	Sun5<em1(IMPC)Mbp>/Sun5<em1(IMPC)Mbp>	C57BL/6N-Sun5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493136	F	MP:0000689	abnormal spleen morphology	Sun5<em1(IMPC)Mbp>/Sun5<em1(IMPC)Mbp>	C57BL/6N-Sun5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493136	F	MP:0003233	prolonged QT interval	Sun5<em1(IMPC)Mbp>/Sun5<em1(IMPC)Mbp>	C57BL/6N-Sun5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493136	M	MP:0003179	thrombocytopenia	Sun5<em1(IMPC)Mbp>/Sun5<em1(IMPC)Mbp>	C57BL/6N-Sun5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493136	F	MP:0000195	decreased circulating calcium level	Sun5<em1(IMPC)Mbp>/Sun5<em1(IMPC)Mbp>	C57BL/6N-Sun5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493137	M	MP:0000198	decreased circulating phosphate level	Surf4<em1(IMPC)J>/Surf4<+>	C57BL/6NJ-Surf4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493137	M	MP:0005293	impaired glucose tolerance	Surf4<em1(IMPC)J>/Surf4<+>	C57BL/6NJ-Surf4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493139	M	MP:0000745	tremors	Syt14<em1(IMPC)J>/Syt14<em1(IMPC)J>	C57BL/6NJ-Syt14<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493140	M	MP:0005567	decreased circulating total protein level	Sytl3<em1(IMPC)Wtsi>/Sytl3<em1(IMPC)Wtsi>	C57BL/6N-Sytl3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493142	M	MP:0005179	decreased circulating cholesterol level	Tagap1<em1(IMPC)Tcp>/Tagap1<em1(IMPC)Tcp>	C57BL/6N-Tagap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493142	F	MP:0005565	increased blood urea nitrogen level	Tagap1<em1(IMPC)Tcp>/Tagap1<em1(IMPC)Tcp>	C57BL/6N-Tagap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493142	M	MP:0002644	decreased circulating triglyceride level	Tagap1<em1(IMPC)Tcp>/Tagap1<em1(IMPC)Tcp>	C57BL/6N-Tagap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493146	M	MP:0002059	abnormal seminal vesicle morphology	Teddm1a<em1(IMPC)Tcp>/Teddm1a<em1(IMPC)Tcp>	C57BL/6N-Teddm1a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493146	M	MP:0000221	decreased leukocyte cell number	Teddm1a<em1(IMPC)Tcp>/Teddm1a<em1(IMPC)Tcp>	C57BL/6N-Teddm1a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493146	F	MP:0002966	decreased circulating alkaline phosphatase level	Teddm1a<em1(IMPC)Tcp>/Teddm1a<em1(IMPC)Tcp>	C57BL/6N-Teddm1a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493146	M	MP:0001925	male infertility	Teddm1a<em1(IMPC)Tcp>/Teddm1a<em1(IMPC)Tcp>	C57BL/6N-Teddm1a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493148	F	MP:0005628	decreased circulating potassium level	Tigit<tm1.1(IMPC)Wtsi>/Tigit<tm1.1(IMPC)Wtsi>	C57BL/6N-Tigit<tm1.1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493149	F	MP:0011965	decreased total retina thickness	Tle1<em1(IMPC)Hmgu>/Tle1<em1(IMPC)Hmgu>	C57BL/6N-Tle1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6493151	M	MP:0001529	abnormal vocalization	Tmc4<em1(IMPC)J>/Tmc4<em1(IMPC)J>	C57BL/6NJ-Tmc4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493151	M	MP:0005655	increased aggression	Tmc4<em1(IMPC)J>/Tmc4<em1(IMPC)J>	C57BL/6NJ-Tmc4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493151	M	MP:0001392	abnormal locomotor behavior	Tmc4<em1(IMPC)J>/Tmc4<em1(IMPC)J>	C57BL/6NJ-Tmc4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493152	M	MP:0003896	prolonged PR interval	Tmco5<tm1b(KOMP)Wtsi>/Tmco5<tm1b(KOMP)Wtsi>	C57BL/6N-Tmco5<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6493153	M	MP:0001697	abnormal embryo size	Tmem131<em1(IMPC)J>/Tmem131<em1(IMPC)J>	C57BL/6NJ-Tmem131<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493153	F	MP:0000428	abnormal craniofacial morphology	Tmem131<em1(IMPC)J>/Tmem131<em1(IMPC)J>	C57BL/6NJ-Tmem131<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493155	M	MP:0020421	increased freezing behavior	Tmem255a<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Tmem255a<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493158	M	MP:0001556	increased circulating HDL cholesterol level	Tmem87b<em1(IMPC)J>/Tmem87b<em1(IMPC)J>	C57BL/6NJ-Tmem87b<em1(IMPC)J>/J	N	MGI:5576271
MGI:6493159	M	MP:0003883	enlarged stomach	Tmem8b<em1(IMPC)Tcp>/Tmem8b<em1(IMPC)Tcp>	C57BL/6N-Tmem8b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493159	M	MP:0002092	abnormal eye morphology	Tmem8b<em1(IMPC)Tcp>/Tmem8b<em1(IMPC)Tcp>	C57BL/6N-Tmem8b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493159	M	MP:0002059	abnormal seminal vesicle morphology	Tmem8b<em1(IMPC)Tcp>/Tmem8b<em1(IMPC)Tcp>	C57BL/6N-Tmem8b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493161	F	MP:0001293	anophthalmia	Togaram1<em1(IMPC)J>/Togaram1<em1(IMPC)J>	C57BL/6NJ-Togaram1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493161	F	MP:0001914	hemorrhage	Togaram1<em1(IMPC)J>/Togaram1<em1(IMPC)J>	C57BL/6NJ-Togaram1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493166	F	MP:0002989	small kidney	Trim61<em1(IMPC)Mbp>/Trim61<em1(IMPC)Mbp>	C57BL/6N-Trim61<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493166	F	MP:0000601	small liver	Trim61<em1(IMPC)Mbp>/Trim61<em1(IMPC)Mbp>	C57BL/6N-Trim61<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493166	F	MP:0000598	abnormal liver morphology	Trim61<em1(IMPC)Mbp>/Trim61<em1(IMPC)Mbp>	C57BL/6N-Trim61<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493167	M	MP:0004002	abnormal jejunum morphology	Trim71<tm1.1(KOMP)Vlcg>/Trim71<+>	C57BL/6N-Trim71<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6493167	M	MP:0002581	abnormal ileum morphology	Trim71<tm1.1(KOMP)Vlcg>/Trim71<+>	C57BL/6N-Trim71<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6493168	M	MP:0005559	increased circulating glucose level	Triobp<em1(IMPC)J>/Triobp<em1(IMPC)J>	C57BL/6NJ-Triobp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493168	F	MP:0009142	decreased prepulse inhibition	Triobp<em1(IMPC)J>/Triobp<em1(IMPC)J>	C57BL/6NJ-Triobp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493168	M	MP:0001284	absent vibrissae	Triobp<em1(IMPC)J>/Triobp<em1(IMPC)J>	C57BL/6NJ-Triobp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493168	F	MP:0001489	decreased startle reflex	Triobp<em1(IMPC)J>/Triobp<em1(IMPC)J>	C57BL/6NJ-Triobp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493169	M	MP:0010052	increased grip strength	Trmt2b<em1(IMPC)J>/Y	C57BL/6NJ-Trmt2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493172	M	MP:0003131	increased erythrocyte cell number	Tstd1<em1(IMPC)J>/Tstd1<em1(IMPC)J>	C57BL/6NJ-Tstd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493172	M	MP:0002608	increased hematocrit	Tstd1<em1(IMPC)J>/Tstd1<em1(IMPC)J>	C57BL/6NJ-Tstd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493176	M	MP:0002075	abnormal coat/hair pigmentation	Ttc7b<em1(IMPC)J>/Ttc7b<+>	C57BL/6NJ-Ttc7b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493180	M	MP:0001399	hyperactivity	Ube2n<em1(IMPC)Ccpcz>/Ube2n<+>	C57BL/6N-Ube2n<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493180	F	MP:0000689	abnormal spleen morphology	Ube2n<em1(IMPC)Ccpcz>/Ube2n<+>	C57BL/6N-Ube2n<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493180	F	MP:0000691	enlarged spleen	Ube2n<em1(IMPC)Ccpcz>/Ube2n<+>	C57BL/6N-Ube2n<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493180	M	MP:0002059	abnormal seminal vesicle morphology	Ube2n<em1(IMPC)Ccpcz>/Ube2n<+>	C57BL/6N-Ube2n<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493180	F	MP:0002932	abnormal joint morphology	Ube2n<em1(IMPC)Ccpcz>/Ube2n<+>	C57BL/6N-Ube2n<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493182	M	MP:0002059	abnormal seminal vesicle morphology	Ubl4b<em1(IMPC)Ccpcz>/Ubl4b<em1(IMPC)Ccpcz>	C57BL/6N-Ubl4b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493182	F	MP:0000709	enlarged thymus	Ubl4b<em1(IMPC)Ccpcz>/Ubl4b<em1(IMPC)Ccpcz>	C57BL/6N-Ubl4b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493182	F	MP:0000703	abnormal thymus morphology	Ubl4b<em1(IMPC)Ccpcz>/Ubl4b<em1(IMPC)Ccpcz>	C57BL/6N-Ubl4b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493182	F	MP:0002060	abnormal skin morphology	Ubl4b<em1(IMPC)Ccpcz>/Ubl4b<em1(IMPC)Ccpcz>	C57BL/6N-Ubl4b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493182	M	MP:0001325	abnormal retina morphology	Ubl4b<em1(IMPC)Ccpcz>/Ubl4b<em1(IMPC)Ccpcz>	C57BL/6N-Ubl4b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493183	M	MP:0001925	male infertility	Ubn2<em1(IMPC)Tcp>/Ubn2<em1(IMPC)Tcp>	C57BL/6N-Ubn2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6493184	M	MP:0005567	decreased circulating total protein level	Ubxn1<em1(IMPC)J>/Ubxn1<em1(IMPC)J>	C57BL/6N-Ubxn1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6493184	M	MP:0002590	increased mean corpuscular volume	Ubxn1<em1(IMPC)J>/Ubxn1<em1(IMPC)J>	C57BL/6N-Ubxn1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6493185	M	MP:0000150	abnormal rib morphology	Uchl4<em1(IMPC)Ccpcz>/Uchl4<em1(IMPC)Ccpcz>	C57BL/6N-Uchl4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493185	F	MP:0013279	increased fasting circulating glucose level	Uchl4<em1(IMPC)Ccpcz>/Uchl4<em1(IMPC)Ccpcz>	C57BL/6N-Uchl4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493188	F	MP:0010392	prolonged QRS complex duration	Usp35<em1(IMPC)J>/Usp35<em1(IMPC)J>	C57BL/6NJ-Usp35<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493189	M	MP:0005655	increased aggression	Vapb<em1(IMPC)H>/Vapb<em1(IMPC)H>	C57BL/6NTac-Vapb<em1(IMPC)H>/H	N	MGI:5576271
MGI:6493189	F	MP:0005292	improved glucose tolerance	Vapb<em1(IMPC)H>/Vapb<em1(IMPC)H>	C57BL/6NTac-Vapb<em1(IMPC)H>/H	N	MGI:5576271
MGI:6493191	M	MP:0005179	decreased circulating cholesterol level	Vil1<em1(IMPC)Wtsi>/Vil1<em1(IMPC)Wtsi>	C57BL/6N-Vil1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493191	M	MP:0010067	increased red blood cell distribution width	Vil1<em1(IMPC)Wtsi>/Vil1<em1(IMPC)Wtsi>	C57BL/6N-Vil1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493191	M	MP:0000186	decreased circulating HDL cholesterol level	Vil1<em1(IMPC)Wtsi>/Vil1<em1(IMPC)Wtsi>	C57BL/6N-Vil1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493191	M	MP:0010088	decreased circulating fructosamine level	Vil1<em1(IMPC)Wtsi>/Vil1<em1(IMPC)Wtsi>	C57BL/6N-Vil1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493192	F	MP:0001120	abnormal uterus morphology	Vwa2<em1(IMPC)Mbp>/Vwa2<em1(IMPC)Mbp>	C57BL/6NCrl-Vwa2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493192	F	MP:0002092	abnormal eye morphology	Vwa2<em1(IMPC)Mbp>/Vwa2<em1(IMPC)Mbp>	C57BL/6NCrl-Vwa2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493192	F	MP:0009709	hydrometra	Vwa2<em1(IMPC)Mbp>/Vwa2<em1(IMPC)Mbp>	C57BL/6NCrl-Vwa2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493193	F	MP:0001297	microphthalmia	Vwc2l<em1(IMPC)Mbp>/Vwc2l<em1(IMPC)Mbp>	C57BL/6NCrl-Vwc2l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493193	F	MP:0002092	abnormal eye morphology	Vwc2l<em1(IMPC)Mbp>/Vwc2l<em1(IMPC)Mbp>	C57BL/6NCrl-Vwc2l<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493194	M	MP:0000702	enlarged lymph nodes	Wdfy3<em1(IMPC)Mbp>/Wdfy3<+>	C57BL/6N-Wdfy3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493194	M	MP:0002135	abnormal kidney morphology	Wdfy3<em1(IMPC)Mbp>/Wdfy3<+>	C57BL/6N-Wdfy3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493194	M	MP:0000598	abnormal liver morphology	Wdfy3<em1(IMPC)Mbp>/Wdfy3<+>	C57BL/6N-Wdfy3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493194	M	MP:0000599	enlarged liver	Wdfy3<em1(IMPC)Mbp>/Wdfy3<+>	C57BL/6N-Wdfy3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493194	M	MP:0002989	small kidney	Wdfy3<em1(IMPC)Mbp>/Wdfy3<+>	C57BL/6N-Wdfy3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493194	M	MP:0002339	abnormal lymph node morphology	Wdfy3<em1(IMPC)Mbp>/Wdfy3<+>	C57BL/6N-Wdfy3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6493196	F	MP:0002060	abnormal skin morphology	Wdr49<em1(IMPC)Ccpcz>/Wdr49<em1(IMPC)Ccpcz>	C57BL/6N-Wdr49<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493196	M	MP:0002981	increased liver weight	Wdr49<em1(IMPC)Ccpcz>/Wdr49<em1(IMPC)Ccpcz>	C57BL/6N-Wdr49<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493196	M	MP:0000266	abnormal heart morphology	Wdr49<em1(IMPC)Ccpcz>/Wdr49<em1(IMPC)Ccpcz>	C57BL/6N-Wdr49<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493199	M	MP:0002075	abnormal coat/hair pigmentation	Yeats2<em1(IMPC)J>/Yeats2<+>	C57BL/6NJ-Yeats2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493199	F	MP:0001399	hyperactivity	Yeats2<em1(IMPC)J>/Yeats2<+>	C57BL/6NJ-Yeats2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493202	F	MP:0009142	decreased prepulse inhibition	Zbtb42<em1(IMPC)Mbp>/Zbtb42<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb42<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493202	F	MP:0000702	enlarged lymph nodes	Zbtb42<em1(IMPC)Mbp>/Zbtb42<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb42<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6493203	M	MP:0001417	decreased exploration in new environment	Zc2hc1a<em1(IMPC)Ccpcz>/Zc2hc1a<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493203	M	MP:0002060	abnormal skin morphology	Zc2hc1a<em1(IMPC)Ccpcz>/Zc2hc1a<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493203	F	MP:0002092	abnormal eye morphology	Zc2hc1a<em1(IMPC)Ccpcz>/Zc2hc1a<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493206	F	MP:0002968	increased circulating alkaline phosphatase level	Zfp423<em1(IMPC)J>/Zfp423<+>	C57BL/6NJ-Zfp423<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493206	F	MP:0001289	persistence of hyaloid vascular system	Zfp423<em1(IMPC)J>/Zfp423<+>	C57BL/6NJ-Zfp423<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493206	F	MP:0001402	decreased locomotor activity	Zfp423<em1(IMPC)J>/Zfp423<+>	C57BL/6NJ-Zfp423<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493207	M	MP:0000367	abnormal coat/ hair morphology	Zfp52<em1(IMPV)J>/Zfp52<em1(IMPV)J>	C57BL/6NJ-Zfp52<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493207	M	MP:0002833	increased heart weight	Zfp52<em1(IMPV)J>/Zfp52<em1(IMPV)J>	C57BL/6NJ-Zfp52<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493208	M	MP:0011110	preweaning lethality, incomplete penetrance	Zfp580<tm1b(EUCOMM)Hmgu>/Zfp580<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp580<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6493209	M	MP:0001146	abnormal testis morphology	Zfp644<em1(IMPC)Ccpcz>/Zfp644<em1(IMPC)Ccpcz>	C57BL/6N-Zfp644<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493209	M	MP:0001262	decreased body weight	Zfp644<em1(IMPC)Ccpcz>/Zfp644<em1(IMPC)Ccpcz>	C57BL/6N-Zfp644<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493209	F	MP:0005562	decreased mean corpuscular hemoglobin	Zfp644<em1(IMPC)Ccpcz>/Zfp644<em1(IMPC)Ccpcz>	C57BL/6N-Zfp644<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493209	F	MP:0004906	enlarged uterus	Zfp644<em1(IMPC)Ccpcz>/Zfp644<em1(IMPC)Ccpcz>	C57BL/6N-Zfp644<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493209	F	MP:0001120	abnormal uterus morphology	Zfp644<em1(IMPC)Ccpcz>/Zfp644<em1(IMPC)Ccpcz>	C57BL/6N-Zfp644<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493209	F	MP:0002968	increased circulating alkaline phosphatase level	Zfp644<em1(IMPC)Ccpcz>/Zfp644<em1(IMPC)Ccpcz>	C57BL/6N-Zfp644<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493209	M	MP:0005627	increased circulating potassium level	Zfp644<em1(IMPC)Ccpcz>/Zfp644<em1(IMPC)Ccpcz>	C57BL/6N-Zfp644<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6493212	M	MP:0001392	abnormal locomotor behavior	Zfp786<em1(IMPC)J>/Zfp786<em1(IMPC)J>	C57BL/6NJ-Zfp786<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493216	F	MP:0010088	decreased circulating fructosamine level	Zmym4<em1(IMPC)Wtsi>/Zmym4<+>	C57BL/6N-Zmym4<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493216	F	MP:0003443	increased circulating glycerol level	Zmym4<em1(IMPC)Wtsi>/Zmym4<+>	C57BL/6N-Zmym4<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493216	F	MP:0000194	increased circulating calcium level	Zmym4<em1(IMPC)Wtsi>/Zmym4<+>	C57BL/6N-Zmym4<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493216	F	MP:0008806	increased circulating amylase level	Zmym4<em1(IMPC)Wtsi>/Zmym4<+>	C57BL/6N-Zmym4<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6493217	F	MP:0001402	decreased locomotor activity	Zyg11b<em1(IMPC)J>/Zyg11b<+>	C57BL/6NJ-Zyg11b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6493217	M	MP:0001417	decreased exploration in new environment	Zyg11b<em1(IMPC)J>/Zyg11b<+>	C57BL/6NJ-Zyg11b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6500995	M	MP:0004852	decreased testis weight	Prdm9<em2Kpgn>/Prdm9<em2Kpgn>	(C57BL/6J-Prdm9<em2Kpgn>/Kpgn x WSB/EiJ)F2	N	33097538
MGI:6500995	M	MP:0001925	male infertility	Prdm9<em2Kpgn>/Prdm9<em2Kpgn>	(C57BL/6J-Prdm9<em2Kpgn>/Kpgn x WSB/EiJ)F2	N	33097538
MGI:6500997	M	MP:0003038	decreased myocardial infarct size	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	32795389
MGI:6500997	M	MP:0002078	abnormal glucose homeostasis	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	32795389
MGI:6500997	F	MP:0030968	decreased circulating adiponectin level	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	23572141
MGI:6500997	M	MP:0030968	decreased circulating adiponectin level	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	23572141
MGI:6500997	M	MP:0009764	decreased susceptibility to induced morbidity/mortality	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	28726787
MGI:6500997	F	MP:0009764	decreased susceptibility to induced morbidity/mortality	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	28726787
MGI:6500997	M	MP:0014142	increased body fat mass	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	23572141
MGI:6500997	F	MP:0014142	increased body fat mass	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	23572141
MGI:6500997	M	MP:0008405	decreased cellular sensitivity to methylmethanesulfonate	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	28726787
MGI:6500997	F	MP:0008405	decreased cellular sensitivity to methylmethanesulfonate	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	28726787
MGI:6500997	F	MP:0003961	decreased lean body mass	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	23572141
MGI:6500997	F	MP:0020102	increased hepatic glucose production	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	23572141
MGI:6500997	F	MP:0003038	decreased myocardial infarct size	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	32795389
MGI:6500997	M	MP:0003037	increased myocardial infarct size	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	32795389
MGI:6500997	F	MP:0002891	increased insulin sensitivity	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	23572141
MGI:6500997	M	MP:0002891	increased insulin sensitivity	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	23572141
MGI:6500997	M	MP:0001764	abnormal homeostasis	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	32795389
MGI:6500997	M	MP:0003961	decreased lean body mass	Alkbh7<tm1.1Klng>/Alkbh7<tm1.1Klng>	involves: 129S2/SvPas * C57BL/6J	N	23572141
MGI:6501007	F	MP:0005389	reproductive system phenotype	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	CAST.129P2(B6)-Prdm9<tm1Ymat>/Hand	Y	33097538
MGI:6501007	M	MP:0001925	male infertility	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	CAST.129P2(B6)-Prdm9<tm1Ymat>/Hand	N	33097538
MGI:6501019	F	MP:0008966	abnormal chiasmata formation	Chek2<tm1b(EUCOMM)Hmgu>/Chek2<tm1b(EUCOMM)Hmgu>,Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.Cg-Chek2<tm1b(EUCOMM)Hmgu> Prdm9<tm1Ymat>	N	33097538
MGI:6501019	F	MP:0004244	abnormal miscarriage rate	Chek2<tm1b(EUCOMM)Hmgu>/Chek2<tm1b(EUCOMM)Hmgu>,Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.Cg-Chek2<tm1b(EUCOMM)Hmgu> Prdm9<tm1Ymat>	N	33097538
MGI:6501019	F	MP:0005168	abnormal female meiosis	Chek2<tm1b(EUCOMM)Hmgu>/Chek2<tm1b(EUCOMM)Hmgu>,Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.Cg-Chek2<tm1b(EUCOMM)Hmgu> Prdm9<tm1Ymat>	N	33097538
MGI:6501019	F	MP:0010767	abnormal female meiosis I arrest	Chek2<tm1b(EUCOMM)Hmgu>/Chek2<tm1b(EUCOMM)Hmgu>,Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.Cg-Chek2<tm1b(EUCOMM)Hmgu> Prdm9<tm1Ymat>	N	33097538
MGI:6501019	F	MP:0001923	reduced female fertility	Chek2<tm1b(EUCOMM)Hmgu>/Chek2<tm1b(EUCOMM)Hmgu>,Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.Cg-Chek2<tm1b(EUCOMM)Hmgu> Prdm9<tm1Ymat>	N	33097538
MGI:6501019	F	MP:0005431	decreased oocyte number	Chek2<tm1b(EUCOMM)Hmgu>/Chek2<tm1b(EUCOMM)Hmgu>,Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.Cg-Chek2<tm1b(EUCOMM)Hmgu> Prdm9<tm1Ymat>	N	33097538
MGI:6501042	M	MP:0001925	male infertility	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.129P2-Prdm9<tm1Ymat>	N	32744506
MGI:6501042	M	MP:0009451	abnormal chromosomal synapsis	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.129P2-Prdm9<tm1Ymat>	N	32744506
MGI:6501042	F	MP:0010767	abnormal female meiosis I arrest	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.129P2-Prdm9<tm1Ymat>	N	33097538
MGI:6501042	M	MP:0010948	abnormal double-strand DNA break repair	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.129P2-Prdm9<tm1Ymat>	N	32744506
MGI:6501042	F	MP:0001926	female infertility	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.129P2-Prdm9<tm1Ymat>	N	33097538
MGI:6501042	F	MP:0008966	abnormal chiasmata formation	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.129P2-Prdm9<tm1Ymat>	N	33097538
MGI:6501042	F	MP:0005168	abnormal female meiosis	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.129P2-Prdm9<tm1Ymat>	N	33097538
MGI:6501754	M	MP:0005332	abnormal amino acid level	Aldh1l2<tm2e(KOMP)Wtsi>/Aldh1l2<tm2e(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	33168096
MGI:6501754	M	MP:0014174	decreased fatty acid beta-oxidation	Aldh1l2<tm2e(KOMP)Wtsi>/Aldh1l2<tm2e(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	33168096
MGI:6501754	M	MP:0030623	decreased cysteine level	Aldh1l2<tm2e(KOMP)Wtsi>/Aldh1l2<tm2e(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	33168096
MGI:6501754	M	MP:0005266	abnormal metabolism	Aldh1l2<tm2e(KOMP)Wtsi>/Aldh1l2<tm2e(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	33168096
MGI:6501754	M	MP:0030685	decreased cystathionine level	Aldh1l2<tm2e(KOMP)Wtsi>/Aldh1l2<tm2e(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	33168096
MGI:6501754	M	MP:0005621	abnormal cell physiology	Aldh1l2<tm2e(KOMP)Wtsi>/Aldh1l2<tm2e(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	33168096
MGI:6501754	M	MP:0011230	abnormal folic acid level	Aldh1l2<tm2e(KOMP)Wtsi>/Aldh1l2<tm2e(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	33168096
MGI:6501754	M	MP:0011229	abnormal vitamin C level	Aldh1l2<tm2e(KOMP)Wtsi>/Aldh1l2<tm2e(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	33168096
MGI:6501754	M	MP:0005319	abnormal enzyme/coenzyme level	Aldh1l2<tm2e(KOMP)Wtsi>/Aldh1l2<tm2e(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	33168096
MGI:6501754	M	MP:0002628	hepatic steatosis	Aldh1l2<tm2e(KOMP)Wtsi>/Aldh1l2<tm2e(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	33168096
MGI:6501754	M	MP:0012604	decreased glutathione level	Aldh1l2<tm2e(KOMP)Wtsi>/Aldh1l2<tm2e(KOMP)Wtsi>	involves: C57BL/6 * C57BL/6N	N	33168096
MGI:6502847	M	MP:0000877	abnormal Purkinje cell morphology	Acbd5<tm1a(EUCOMM)Wtsi>/Acbd5<tm1a(EUCOMM)Wtsi>	C57BL/6N-A<tm1Brd> Acbd5<tm1a(EUCOMM)Wtsi>/WtsiCnbc	N	33244184
MGI:6502847	M	MP:0005404	abnormal axon morphology	Acbd5<tm1a(EUCOMM)Wtsi>/Acbd5<tm1a(EUCOMM)Wtsi>	C57BL/6N-A<tm1Brd> Acbd5<tm1a(EUCOMM)Wtsi>/WtsiCnbc	N	33244184
MGI:6502847	M	MP:0000607	abnormal hepatocyte morphology	Acbd5<tm1a(EUCOMM)Wtsi>/Acbd5<tm1a(EUCOMM)Wtsi>	C57BL/6N-A<tm1Brd> Acbd5<tm1a(EUCOMM)Wtsi>/WtsiCnbc	N	33244184
MGI:6502847	M	MP:0000880	decreased Purkinje cell number	Acbd5<tm1a(EUCOMM)Wtsi>/Acbd5<tm1a(EUCOMM)Wtsi>	C57BL/6N-A<tm1Brd> Acbd5<tm1a(EUCOMM)Wtsi>/WtsiCnbc	N	33244184
MGI:6502847	M	MP:0000876	Purkinje cell degeneration	Acbd5<tm1a(EUCOMM)Wtsi>/Acbd5<tm1a(EUCOMM)Wtsi>	C57BL/6N-A<tm1Brd> Acbd5<tm1a(EUCOMM)Wtsi>/WtsiCnbc	N	33244184
MGI:6502847	M	MP:0000598	abnormal liver morphology	Acbd5<tm1a(EUCOMM)Wtsi>/Acbd5<tm1a(EUCOMM)Wtsi>	C57BL/6N-A<tm1Brd> Acbd5<tm1a(EUCOMM)Wtsi>/WtsiCnbc	N	33244184
MGI:6506200	M	MP:0003961	decreased lean body mass	Zfp30<em1Snpk>/Zfp30<em1Snpk>	C57BL/6J-Zfp30<em1Snpk>/Mmnc	N	32860515
MGI:6506200	M	MP:0001262	decreased body weight	Zfp30<em1Snpk>/Zfp30<em1Snpk>	C57BL/6J-Zfp30<em1Snpk>/Mmnc	N	32860515
MGI:6506200	F	MP:0011101	prenatal lethality, incomplete penetrance	Zfp30<em1Snpk>/Zfp30<em1Snpk>	C57BL/6J-Zfp30<em1Snpk>/Mmnc	N	32860515
MGI:6506256	F	MP:0001376	abnormal mating receptivity	Vmn2r115<em1Ktou>/Vmn2r115<em1Ktou>	involves: C57BL/6J	N	30367054
MGI:6506257	F	MP:0002243	abnormal vomeronasal organ morphology	Vmn2r117<em1Ktou>/Vmn2r117<em1Ktou>	involves: C57BL/6J	N	30367054
MGI:6506259	F	MP:0013596	abnormal vomeronasal organ physiology	Vmn2r116<tm1.1Ktou>/Vmn2r116<tm1.1Ktou>	involves: C57BL/6	N	30367054
MGI:6506259	F	MP:0002243	abnormal vomeronasal organ morphology	Vmn2r116<tm1.1Ktou>/Vmn2r116<tm1.1Ktou>	involves: C57BL/6	N	30367054
MGI:6506273	M	MP:0005293	impaired glucose tolerance	Uox<em1Cli>/Uox<em1Cli>	C57BL/6J-Uox<em1Cli>	N	28729031
MGI:6506273	F	MP:0002842	increased systemic arterial blood pressure	Uox<em1Cli>/Uox<em1Cli>	C57BL/6J-Uox<em1Cli>	N	28729031
MGI:6506273	M	MP:0009114	decreased pancreatic beta cell mass	Uox<em1Cli>/Uox<em1Cli>	C57BL/6J-Uox<em1Cli>	N	28729031
MGI:6506273	F	MP:0001552	increased circulating triglyceride level	Uox<em1Cli>/Uox<em1Cli>	C57BL/6J-Uox<em1Cli>	N	28729031
MGI:6506273	M	MP:0014117	increased pancreatic beta cell apoptosis	Uox<em1Cli>/Uox<em1Cli>	C57BL/6J-Uox<em1Cli>	N	28729031
MGI:6506273	F	MP:0005178	increased circulating cholesterol level	Uox<em1Cli>/Uox<em1Cli>	C57BL/6J-Uox<em1Cli>	N	28729031
MGI:6506273	F	MP:0000182	increased circulating LDL cholesterol level	Uox<em1Cli>/Uox<em1Cli>	C57BL/6J-Uox<em1Cli>	N	28729031
MGI:6506273	M	MP:0003059	decreased insulin secretion	Uox<em1Cli>/Uox<em1Cli>	C57BL/6J-Uox<em1Cli>	N	28729031
MGI:6506273	M	MP:0002644	decreased circulating triglyceride level	Uox<em1Cli>/Uox<em1Cli>	C57BL/6J-Uox<em1Cli>	N	28729031
MGI:6506382	M	MP:0009451	abnormal chromosomal synapsis	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	B6N(Cg)-Stag3<tm1e.1(KOMP)Wtsi>	N	30853435
MGI:6506382	M	MP:0014052	increased male germ cell apoptosis	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	B6N(Cg)-Stag3<tm1e.1(KOMP)Wtsi>	N	30853435
MGI:6506382	M	MP:0009452	abnormal synaptonemal complex	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	B6N(Cg)-Stag3<tm1e.1(KOMP)Wtsi>	N	30853435
MGI:6506382	M	MP:0010948	abnormal double-strand DNA break repair	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	B6N(Cg)-Stag3<tm1e.1(KOMP)Wtsi>	N	30853435
MGI:6506382	M	MP:0005169	abnormal male meiosis	Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	B6N(Cg)-Stag3<tm1e.1(KOMP)Wtsi>	N	30853435
MGI:6506386	M	MP:0010948	abnormal double-strand DNA break repair	Rec8<tm1b(KOMP)Wtsi>/Rec8<tm1b(KOMP)Wtsi>	B6N(Cg)-Rec8<tm1b(KOMP)Wtsi>	N	30853435
MGI:6506386	M	MP:0005169	abnormal male meiosis	Rec8<tm1b(KOMP)Wtsi>/Rec8<tm1b(KOMP)Wtsi>	B6N(Cg)-Rec8<tm1b(KOMP)Wtsi>	N	30853435
MGI:6506388	M	MP:0005384	cellular phenotype	Rad21l<tm1b(KOMP)Wtsi>/Rad21l<tm1b(KOMP)Wtsi>	B6N(Cg)-Rad21l<tm1b(KOMP)Wtsi>	Y	30853435
MGI:6506390	M	MP:0010948	abnormal double-strand DNA break repair	Rec8<tm1b(KOMP)Wtsi>/Rec8<tm1b(KOMP)Wtsi>,Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	B6N(Cg)-Rec8<tm1b(KOMP)Wtsi> Stag3<tm1e.1(KOMP)Wtsi>	N	30853435
MGI:6506390	M	MP:0005169	abnormal male meiosis	Rec8<tm1b(KOMP)Wtsi>/Rec8<tm1b(KOMP)Wtsi>,Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	B6N(Cg)-Rec8<tm1b(KOMP)Wtsi> Stag3<tm1e.1(KOMP)Wtsi>	N	30853435
MGI:6506390	M	MP:0009452	abnormal synaptonemal complex	Rec8<tm1b(KOMP)Wtsi>/Rec8<tm1b(KOMP)Wtsi>,Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	B6N(Cg)-Rec8<tm1b(KOMP)Wtsi> Stag3<tm1e.1(KOMP)Wtsi>	N	30853435
MGI:6506392	M	MP:0010948	abnormal double-strand DNA break repair	Rad21l<tm1b(KOMP)Wtsi>/Rad21l<tm1b(KOMP)Wtsi>,Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	B6N(Cg)-Rad21l<tm1b(KOMP)Wtsi> Stag3<tm1e.1(KOMP)Wtsi>	N	30853435
MGI:6506392	M	MP:0009452	abnormal synaptonemal complex	Rad21l<tm1b(KOMP)Wtsi>/Rad21l<tm1b(KOMP)Wtsi>,Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	B6N(Cg)-Rad21l<tm1b(KOMP)Wtsi> Stag3<tm1e.1(KOMP)Wtsi>	N	30853435
MGI:6506394	M	MP:0010948	abnormal double-strand DNA break repair	Rad21l<tm1b(KOMP)Wtsi>/Rad21l<tm1b(KOMP)Wtsi>,Rec8<tm1b(KOMP)Wtsi>/Rec8<tm1b(KOMP)Wtsi>	B6N(Cg)-Rad21l<tm1b(KOMP)Wtsi> Rec8<tm1b(KOMP)Wtsi>	N	30853435
MGI:6506404	M	MP:0005384	cellular phenotype	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>,Rad21l<tm1b(KOMP)Wtsi>/Rad21l<tm1b(KOMP)Wtsi>	B6.Cg-Prdm9<tm1Ymat> Rad21l<tm1b(KOMP)Wtsi>	Y	30853435
MGI:6506408	M	MP:0010948	abnormal double-strand DNA break repair	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>,Rec8<tm1b(KOMP)Wtsi>/Rec8<tm1b(KOMP)Wtsi>	B6.Cg-Prdm9<tm1Ymat> Rec8<tm1b(KOMP)Wtsi>	N	30853435
MGI:6506415	M	MP:0005169	abnormal male meiosis	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>,Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	B6.Cg-Prdm9<tm1Ymat> Stag3<tm1e.1(KOMP)Wtsi>	N	30853435
MGI:6506415	M	MP:0010948	abnormal double-strand DNA break repair	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>,Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	B6.Cg-Prdm9<tm1Ymat> Stag3<tm1e.1(KOMP)Wtsi>	N	30853435
MGI:6506420	M	MP:0005384	cellular phenotype	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.Cg-Prdm9<tm1Ymat>	Y	30853435
MGI:6506420	M	MP:0005389	reproductive system phenotype	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	B6.Cg-Prdm9<tm1Ymat>	Y	30853435
MGI:6506421	M	MP:0005384	cellular phenotype	Prdm9<em3Kpgn>/Prdm9<em3Kpgn>	involves: C57BL/6J	Y	30853435
MGI:6506422	M	MP:0010948	abnormal double-strand DNA break repair	Prdm9<em3Kpgn>/Prdm9<em3Kpgn>,Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	involves: C57BL/6J * C57BL/6N	N	30853435
MGI:6506424	M	MP:0010948	abnormal double-strand DNA break repair	Spo11<tm1Mjn>/Spo11<+>	B6.Cg-Spo11<tm1Mjn>	N	30853435
MGI:6506426	M	MP:0010948	abnormal double-strand DNA break repair	Spo11<tm1Mjn>/Spo11<+>,Stag3<tm1e.1(KOMP)Wtsi>/Stag3<tm1e.1(KOMP)Wtsi>	B6.Cg-Spo11<tm1Mjn> Stag3<tm1e.1(KOMP)Wtsi>/2J	N	30853435
MGI:6507170	M	MP:0011089	perinatal lethality, complete penetrance	Phf6<tm1.2Avo>/Y	involves: BALB/cJ * C57BL/6	N	30755422
MGI:6507170	M	MP:0011089	perinatal lethality, complete penetrance	Phf6<tm1.2Avo>/Y	involves: BALB/cJ * C57BL/6	N	32994169
MGI:6507171	F	MP:0001262	decreased body weight	Phf6<tm1.2Avo>/Phf6<+>	involves: BALB/cJ * C57BL/6	N	32994169
MGI:6507171	F	MP:0002026	increased leukemia incidence	Phf6<tm1.2Avo>/Phf6<+>	involves: BALB/cJ * C57BL/6	N	30755422
MGI:6507173	M	MP:0011902	increased hematopoietic stem cell proliferation	Phf6<tm1.1Avo>/Y,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	30755422
MGI:6507173	M	MP:0004809	increased hematopoietic stem cell number	Phf6<tm1.1Avo>/Y,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	30755422
MGI:6507173	M	MP:0002026	increased leukemia incidence	Phf6<tm1.1Avo>/Y,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	30755422
MGI:6507173	M	MP:0004810	decreased hematopoietic stem cell number	Phf6<tm1.1Avo>/Y,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	30755422
MGI:6507173	M	MP:0014400	increased hematopoietic precursor cell number	Phf6<tm1.1Avo>/Y,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	30755422
MGI:6507173	M	MP:0008524	increased plasmacytoid dendritic cell number	Phf6<tm1.1Avo>/Y,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	30755422
MGI:6507173	M	MP:0001545	abnormal hematopoietic system physiology	Phf6<tm1.1Avo>/Y,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	30755422
MGI:6507173	M	MP:0008573	increased circulating interferon-alpha level	Phf6<tm1.1Avo>/Y,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	30755422
MGI:6507173	M	MP:0010132	decreased DN2 thymocyte number	Phf6<tm1.1Avo>/Y,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	30755422
MGI:6507173	M	MP:0013892	increased common lymphocyte progenitor cell number	Phf6<tm1.1Avo>/Y,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	30755422
MGI:6507173	M	MP:0013707	abnormal hematopoietic precursor cell morphology	Phf6<tm1.1Avo>/Y,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	30755422
MGI:6507173	M	MP:0002145	abnormal T cell differentiation	Phf6<tm1.1Avo>/Y,Tg(Tek-cre)1Ywa/0	involves: C57BL/6 * SJL	N	30755422
MGI:6507205	M	MP:0005389	reproductive system phenotype	Phf6<tm1.2Avo>/Y	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	Y	32994169
MGI:6507205	M	MP:0005361	small pituitary gland	Phf6<tm1.2Avo>/Y	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	N	32994169
MGI:6507205	M	MP:0000008	increased white adipose tissue amount	Phf6<tm1.2Avo>/Y	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	N	32994169
MGI:6507205	M	MP:0005120	decreased circulating growth hormone level	Phf6<tm1.2Avo>/Y	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	N	32994169
MGI:6507205	M	MP:0005128	decreased adrenocorticotropin level	Phf6<tm1.2Avo>/Y	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	N	32994169
MGI:6507205	M	MP:0005136	decreased growth hormone level	Phf6<tm1.2Avo>/Y	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	N	32994169
MGI:6507205	M	MP:0004701	decreased circulating insulin-like growth factor I level	Phf6<tm1.2Avo>/Y	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	N	32994169
MGI:6507205	M	MP:0005138	decreased prolactin level	Phf6<tm1.2Avo>/Y	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	N	32994169
MGI:6507205	M	MP:0011086	postnatal lethality, incomplete penetrance	Phf6<tm1.2Avo>/Y	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	N	32994169
MGI:6507205	M	MP:0001265	decreased body size	Phf6<tm1.2Avo>/Y	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	N	32994169
MGI:6507205	M	MP:0010768	mortality/aging	Phf6<tm1.2Avo>/Y	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	Y	32994169
MGI:6507205	M	MP:0003961	decreased lean body mass	Phf6<tm1.2Avo>/Y	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	N	32994169
MGI:6507205	M	MP:0001262	decreased body weight	Phf6<tm1.2Avo>/Y	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	N	32994169
MGI:6507210	F	MP:0001265	decreased body size	Phf6<tm1.2Avo>/Phf6<tm1.2Avo>	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	N	32994169
MGI:6507211	M	MP:0001265	decreased body size	Phf6<tm1.1Avo>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	32994169
MGI:6507211	M	MP:0001262	decreased body weight	Phf6<tm1.1Avo>/Y,Tg(Nes-cre)1Kln/0	involves: C57BL/6 * SJL	N	32994169
MGI:6507212	M	MP:0005378	growth/size/body region phenotype	Phf6<tm1.2Avo>/Y,Socs2<tm1Wehi>/Socs2<tm1Wehi>	involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	Y	32994169
MGI:6507848	M	MP:0020879	abnormal calcium level	Dmd<mdx>/Y,Tg(DMD*)#Spc/0	involves: 129P2/OlaHsd * C57BL/10ScSn * DBA/2	N	28505980
MGI:6507848	M	MP:0004510	myositis	Dmd<mdx>/Y,Tg(DMD*)#Spc/0	involves: 129P2/OlaHsd * C57BL/10ScSn * DBA/2	N	28505980
MGI:6507848	M	MP:0009419	skeletal muscle fibrosis	Dmd<mdx>/Y,Tg(DMD*)#Spc/0	involves: 129P2/OlaHsd * C57BL/10ScSn * DBA/2	N	28505980
MGI:6507848	M	MP:0000752	dystrophic muscle	Dmd<mdx>/Y,Tg(DMD*)#Spc/0	involves: 129P2/OlaHsd * C57BL/10ScSn * DBA/2	N	28505980
MGI:6507866	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Igs2<tm1(CAG-Met)Zsu>/Igs2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129 * C57BL/6 * DBA/2 * FVB/N	N	30401749
MGI:6507866	M	MP:0010357	increased prostate gland tumor incidence	Igs2<tm1(CAG-Met)Zsu>/Igs2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129 * C57BL/6 * DBA/2 * FVB/N	N	30401749
MGI:6507866	M	MP:0001272	increased metastatic potential	Igs2<tm1(CAG-Met)Zsu>/Igs2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129 * C57BL/6 * DBA/2 * FVB/N	N	30401749
MGI:6507866	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Igs2<tm1(CAG-Met)Zsu>/Igs2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129 * C57BL/6 * DBA/2 * FVB/N	N	30401749
MGI:6507866	M	MP:0002038	increased carcinoma incidence	Igs2<tm1(CAG-Met)Zsu>/Igs2<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pbsn-cre)4Prb/0	involves: 129 * C57BL/6 * DBA/2 * FVB/N	N	30401749
MGI:6507888	M	MP:0009220	increased prostate gland adenocarcinoma incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Igs2<tm1(CAG-Met)Zsu>/Igs2<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2 * FVB/N	N	31819003
MGI:6507888	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Ctnnb1<tm1Mmt>/Ctnnb1<+>,Igs2<tm1(CAG-Met)Zsu>/Igs2<+>,Tg(Pbsn-cre)4Prb/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2 * FVB/N	N	31819003
MGI:6508101	M	MP:0014052	increased male germ cell apoptosis	Fancm<em1Qsh>/Fancm<em1Qsh>	C57BL/6-Fancm<em1Qsh>	N	29895858
MGI:6508101	M	MP:0005397	hematopoietic system phenotype	Fancm<em1Qsh>/Fancm<em1Qsh>	C57BL/6-Fancm<em1Qsh>	Y	29895858
MGI:6508101	M	MP:0006380	abnormal spermatid morphology	Fancm<em1Qsh>/Fancm<em1Qsh>	C57BL/6-Fancm<em1Qsh>	N	29895858
MGI:6508101	M	MP:0002006	neoplasm	Fancm<em1Qsh>/Fancm<em1Qsh>	C57BL/6-Fancm<em1Qsh>	Y	29895858
MGI:6508101	M	MP:0014040	increased cellular sensitivity to DNA damaging agents	Fancm<em1Qsh>/Fancm<em1Qsh>	C57BL/6-Fancm<em1Qsh>	N	29895858
MGI:6508101	M	MP:0001925	male infertility	Fancm<em1Qsh>/Fancm<em1Qsh>	C57BL/6-Fancm<em1Qsh>	N	29895858
MGI:6508101	M	MP:0002216	abnormal seminiferous tubule morphology	Fancm<em1Qsh>/Fancm<em1Qsh>	C57BL/6-Fancm<em1Qsh>	N	29895858
MGI:6508101	M	MP:0001154	seminiferous tubule degeneration	Fancm<em1Qsh>/Fancm<em1Qsh>	C57BL/6-Fancm<em1Qsh>	N	29895858
MGI:6508378	M	MP:0014142	increased body fat mass	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	N	21971119
MGI:6508378	M	MP:0001260	increased body weight	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	N	21971119
MGI:6508378	M	MP:0009288	increased epididymal fat pad weight	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	N	21971119
MGI:6508378	M	MP:0005669	increased circulating leptin level	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	N	21971119
MGI:6508378	M	MP:0009355	increased liver triglyceride level	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	N	21971119
MGI:6508378	M	MP:0002981	increased liver weight	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	N	21971119
MGI:6508378	M	MP:0009298	increased mesenteric fat pad weight	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	N	21971119
MGI:6508378	M	MP:0001552	increased circulating triglyceride level	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	N	21971119
MGI:6508378	M	MP:0005645	abnormal hypothalamus physiology	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	N	21971119
MGI:6508378	M	MP:0005386	behavior/neurological phenotype	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	Y	21971119
MGI:6508378	M	MP:0009286	increased abdominal fat pad weight	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	N	21971119
MGI:6508378	M	MP:0009304	increased retroperitoneal fat pad weight	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	N	21971119
MGI:6508378	M	MP:0005376	homeostasis/metabolism phenotype	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	Y	21971119
MGI:6508378	M	MP:0020867	increased lipogenesis	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	N	21971119
MGI:6508378	M	MP:0002079	increased circulating insulin level	Gpr61<tm1Dgen>/Gpr61<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6J	N	21971119
MGI:6508384	M	MP:0009325	necrospermia	Kcng4<tm1(KOMP)Vlcg>/Kcng4<tm1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1(KOMP)Vlcg>	N	27677211
MGI:6508384	M	MP:0001156	abnormal spermatogenesis	Kcng4<tm1(KOMP)Vlcg>/Kcng4<tm1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1(KOMP)Vlcg>	N	27677211
MGI:6508384	M	MP:0020451	decreased sperm progressive motility	Kcng4<tm1(KOMP)Vlcg>/Kcng4<tm1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1(KOMP)Vlcg>	N	27677211
MGI:6508384	M	MP:0009230	abnormal sperm head morphology	Kcng4<tm1(KOMP)Vlcg>/Kcng4<tm1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1(KOMP)Vlcg>	N	27677211
MGI:6508384	M	MP:0005578	teratozoospermia	Kcng4<tm1(KOMP)Vlcg>/Kcng4<tm1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1(KOMP)Vlcg>	N	27677211
MGI:6508384	M	MP:0001932	abnormal spermiogenesis	Kcng4<tm1(KOMP)Vlcg>/Kcng4<tm1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1(KOMP)Vlcg>	N	27677211
MGI:6508384	M	MP:0002687	oligozoospermia	Kcng4<tm1(KOMP)Vlcg>/Kcng4<tm1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1(KOMP)Vlcg>	N	27677211
MGI:6508384	M	MP:0009235	small sperm head	Kcng4<tm1(KOMP)Vlcg>/Kcng4<tm1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1(KOMP)Vlcg>	N	27677211
MGI:6508384	M	MP:0009831	abnormal sperm midpiece morphology	Kcng4<tm1(KOMP)Vlcg>/Kcng4<tm1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1(KOMP)Vlcg>	N	27677211
MGI:6508384	M	MP:0006380	abnormal spermatid morphology	Kcng4<tm1(KOMP)Vlcg>/Kcng4<tm1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1(KOMP)Vlcg>	N	27677211
MGI:6508384	M	MP:0009239	short sperm flagellum	Kcng4<tm1(KOMP)Vlcg>/Kcng4<tm1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1(KOMP)Vlcg>	N	27677211
MGI:6508384	M	MP:0002675	asthenozoospermia	Kcng4<tm1(KOMP)Vlcg>/Kcng4<tm1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1(KOMP)Vlcg>	N	27677211
MGI:6508384	M	MP:0001925	male infertility	Kcng4<tm1(KOMP)Vlcg>/Kcng4<tm1(KOMP)Vlcg>	C57BL/6N-Kcng4<tm1(KOMP)Vlcg>	N	27677211
MGI:6508527	M	MP:0003999	enhanced passive avoidance behavior	Slc9a5<tm1Smoc>/Slc9a5<tm1Smoc>	involves: C57BL/6	N	28981195
MGI:6508527	M	MP:0012314	enhanced learning	Slc9a5<tm1Smoc>/Slc9a5<tm1Smoc>	involves: C57BL/6	N	28981195
MGI:6508527	M	MP:0005386	behavior/neurological phenotype	Slc9a5<tm1Smoc>/Slc9a5<tm1Smoc>	involves: C57BL/6	Y	28981195
MGI:6508527	M	MP:0001458	abnormal object recognition memory	Slc9a5<tm1Smoc>/Slc9a5<tm1Smoc>	involves: C57BL/6	N	28981195
MGI:6508527	M	MP:0003633	abnormal nervous system physiology	Slc9a5<tm1Smoc>/Slc9a5<tm1Smoc>	involves: C57BL/6	N	28981195
MGI:6508527	M	MP:0009538	abnormal synapse morphology	Slc9a5<tm1Smoc>/Slc9a5<tm1Smoc>	involves: C57BL/6	N	28981195
MGI:6508527	M	MP:0008414	abnormal spatial reference memory	Slc9a5<tm1Smoc>/Slc9a5<tm1Smoc>	involves: C57BL/6	N	28981195
MGI:6508693	M	MP:0008938	decreased pituitary gland weight	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0031362	decreased prostate gland ventral lobe weight	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0004952	increased spleen weight	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0001153	small seminiferous tubules	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0003953	abnormal hormone level	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0013602	abnormal Leydig cell differentiation	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0014142	increased body fat mass	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0003918	decreased kidney weight	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0005189	abnormal anogenital distance	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0004852	decreased testis weight	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0001156	abnormal spermatogenesis	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0004910	decreased seminal vesicle weight	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0002784	abnormal Sertoli cell morphology	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0002781	increased circulating testosterone level	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0004929	decreased epididymis weight	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0001751	increased circulating luteinizing hormone level	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0002108	abnormal muscle morphology	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0005186	increased circulating progesterone level	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0009819	abnormal circulating androgen level	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0008940	delayed balanopreputial separation	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0001922	reduced male fertility	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0001260	increased body weight	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0003509	increased circulating dihydrotestosterone level	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0011384	abnormal progesterone level	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6508693	M	MP:0011385	abnormal testosterone level	Hsd17b3<tm1.2Mpo>/Hsd17b3<tm1.2Mpo>	involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	N	32190925
MGI:6509044	M	MP:0005389	reproductive system phenotype	Prps1l1<em1Wyan>/Prps1l1<em1Wyan>	involves: C57BL/6J * FVB/NJ	Y	30113107
MGI:6509048	M	MP:0005389	reproductive system phenotype	Lypd9<em1Juhu>/Lypd9<em1Juhu>	Not Specified	Y	29247571
MGI:6509983	F	MP:0001934	increased litter size	Sfrp2<tm1.1Brle>/Sfrp2<tm1.1Brle>,Sfrp4<tm1.1Boer>/Sfrp4<tm1.1Boer>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * BALB/cJ	N	30942852
MGI:6509983	F	MP:0031411	increased ovulation rate	Sfrp2<tm1.1Brle>/Sfrp2<tm1.1Brle>,Sfrp4<tm1.1Boer>/Sfrp4<tm1.1Boer>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * BALB/cJ	N	30942852
MGI:6509984	F	MP:0001130	abnormal ovarian folliculogenesis	Sfrp4<tm1.1Boer>/Sfrp4<tm1.1Boer>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ	N	30942852
MGI:6509984	F	MP:0008870	increased mature ovarian follicle number	Sfrp4<tm1.1Boer>/Sfrp4<tm1.1Boer>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ	N	30942852
MGI:6509984	F	MP:0001934	increased litter size	Sfrp4<tm1.1Boer>/Sfrp4<tm1.1Boer>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ	N	30942852
MGI:6510016	M	MP:0002687	oligozoospermia	Spata31<tm1Yangy>/Spata31<tm1Yangy>,Tg(Ddx4-cre)1Dcas/0	involves: 129S7/SvEvBrd * FVB	N	25930072
MGI:6510016	M	MP:0001925	male infertility	Spata31<tm1Yangy>/Spata31<tm1Yangy>,Tg(Ddx4-cre)1Dcas/0	involves: 129S7/SvEvBrd * FVB	N	25930072
MGI:6510016	M	MP:0001147	small testis	Spata31<tm1Yangy>/Spata31<tm1Yangy>,Tg(Ddx4-cre)1Dcas/0	involves: 129S7/SvEvBrd * FVB	N	25930072
MGI:6510016	M	MP:0001146	abnormal testis morphology	Spata31<tm1Yangy>/Spata31<tm1Yangy>,Tg(Ddx4-cre)1Dcas/0	involves: 129S7/SvEvBrd * FVB	N	25930072
MGI:6510016	M	MP:0006380	abnormal spermatid morphology	Spata31<tm1Yangy>/Spata31<tm1Yangy>,Tg(Ddx4-cre)1Dcas/0	involves: 129S7/SvEvBrd * FVB	N	25930072
MGI:6510016	M	MP:0004182	abnormal spermiation	Spata31<tm1Yangy>/Spata31<tm1Yangy>,Tg(Ddx4-cre)1Dcas/0	involves: 129S7/SvEvBrd * FVB	N	25930072
MGI:6510016	M	MP:0005578	teratozoospermia	Spata31<tm1Yangy>/Spata31<tm1Yangy>,Tg(Ddx4-cre)1Dcas/0	involves: 129S7/SvEvBrd * FVB	N	25930072
MGI:6510020	M	MP:0020451	decreased sperm progressive motility	Spata19<tm1Lij>/Spata19<tm1Lij>,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * FVB/NJ	N	26265198
MGI:6510020	M	MP:0010955	abnormal respiratory electron transport chain	Spata19<tm1Lij>/Spata19<tm1Lij>,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * FVB/NJ	N	26265198
MGI:6510020	M	MP:0001925	male infertility	Spata19<tm1Lij>/Spata19<tm1Lij>,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * FVB/NJ	N	26265198
MGI:6510020	M	MP:0008892	abnormal sperm flagellum morphology	Spata19<tm1Lij>/Spata19<tm1Lij>,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * FVB/NJ	N	26265198
MGI:6510020	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Spata19<tm1Lij>/Spata19<tm1Lij>,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * FVB/NJ	N	26265198
MGI:6510020	M	MP:0014465	abnormal sperm mitochondrial morphology	Spata19<tm1Lij>/Spata19<tm1Lij>,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * FVB/NJ	N	26265198
MGI:6510630	M	MP:0005178	increased circulating cholesterol level	Slc10a6<tm1Jmge>/Slc10a6<tm1Jmge>	B6N.129S5-Slc10a6<tm1Jmge>	N	28743544
MGI:6510793	F	MP:0001473	reduced long-term potentiation	Tspan6<tm2Vlcg>/Tspan6<tm2Vlcg>	involves: 129P2/OlaHsd * C57BL/6	N	28207852
MGI:6510793	F	MP:0002912	abnormal excitatory postsynaptic potential	Tspan6<tm2Vlcg>/Tspan6<tm2Vlcg>	involves: 129P2/OlaHsd * C57BL/6	N	28207852
MGI:6510793	F	MP:0002206	abnormal CNS synaptic transmission	Tspan6<tm2Vlcg>/Tspan6<tm2Vlcg>	involves: 129P2/OlaHsd * C57BL/6	N	28207852
MGI:6510793	F	MP:0003631	nervous system phenotype	Tspan6<tm2Vlcg>/Tspan6<tm2Vlcg>	involves: 129P2/OlaHsd * C57BL/6	Y	28207852
MGI:6510794	M	MP:0005386	behavior/neurological phenotype	Tspan6<tm2Vlcg>/Y	involves: 129P2/OlaHsd * C57BL/6	Y	28207852
MGI:6510794	M	MP:0002804	abnormal motor learning	Tspan6<tm2Vlcg>/Y	involves: 129P2/OlaHsd * C57BL/6	N	28207852
MGI:6510865	F	MP:0005452	abnormal adipose tissue amount	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0005292	improved glucose tolerance	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0005533	increased body temperature	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0011940	decreased food intake	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0002727	decreased circulating insulin level	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0010025	decreased total body fat amount	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0003960	increased lean body mass	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0005318	decreased triglyceride level	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0002891	increased insulin sensitivity	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0020477	abnormal locomotor circadian rhythm	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0001973	increased thermal nociceptive threshold	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0001402	decreased locomotor activity	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0005146	decreased circulating VLDL cholesterol level	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0009269	decreased fat cell size	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510865	F	MP:0001262	decreased body weight	Gpr82<tm1Shbg>/Gpr82<tm1Shbg>	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0005146	decreased circulating VLDL cholesterol level	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0003960	increased lean body mass	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0011940	decreased food intake	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0005318	decreased triglyceride level	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0020477	abnormal locomotor circadian rhythm	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0010182	decreased susceptibility to weight gain	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0005560	decreased circulating glucose level	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0001973	increased thermal nociceptive threshold	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0005452	abnormal adipose tissue amount	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0005533	increased body temperature	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0013278	decreased fasting circulating glucose level	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0005292	improved glucose tolerance	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0002727	decreased circulating insulin level	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0001402	decreased locomotor activity	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0001262	decreased body weight	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0009269	decreased fat cell size	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6510869	M	MP:0010025	decreased total body fat amount	Gpr82<tm1Shbg>/Y	C3Fe.Cg-Gpr82<tm1Shbg>	N	22216272
MGI:6511033	M	MP:0020421	increased freezing behavior	Or5ar1<tm1Hsak>/?	Not Specified	N	28685774
MGI:6511034	M	MP:0020422	decreased freezing behavior	Or5ar1<tm2Hsak>/Or5ar1<tm2Hsak>	Not Specified	N	28685774
MGI:6512404	F	MP:0009223	increased uterus carcinoma incidence	Pten<tm1.2Mwst>/Pten<+>	involves: 129S6/SvEvTac * Black Swiss * FVB/N	N	20194734
MGI:6512404	F	MP:0009092	endometrium hyperplasia	Pten<tm1.2Mwst>/Pten<+>	involves: 129S6/SvEvTac * Black Swiss * FVB/N	N	20194734
MGI:6512404	M	MP:0010357	increased prostate gland tumor incidence	Pten<tm1.2Mwst>/Pten<+>	involves: 129S6/SvEvTac * Black Swiss * FVB/N	N	20194734
MGI:6512503	M	MP:0002675	asthenozoospermia	Cfap45<em1Hmd>/Cfap45<em1Hmd>	involves: C57BL/6	N	33139725
MGI:6512503	M	MP:0009282	decreased hyperactivated sperm motility	Cfap45<em1Hmd>/Cfap45<em1Hmd>	involves: C57BL/6	N	33139725
MGI:6512503	M	MP:0001925	male infertility	Cfap45<em1Hmd>/Cfap45<em1Hmd>	involves: C57BL/6	N	33139725
MGI:6513091	M	MP:0014468	disorganized sperm mitochondrial sheath	Armc12<em1Osb>/Armc12<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	33536340
MGI:6513091	M	MP:0030978	impaired binding of sperm to zona pellucida	Armc12<em1Osb>/Armc12<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	33536340
MGI:6513091	M	MP:0009237	kinked sperm flagellum	Armc12<em1Osb>/Armc12<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	33536340
MGI:6513091	M	MP:0001925	male infertility	Armc12<em1Osb>/Armc12<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	33536340
MGI:6513091	M	MP:0009647	decreased fertilization frequency	Armc12<em1Osb>/Armc12<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	33536340
MGI:6513091	M	MP:0020451	decreased sperm progressive motility	Armc12<em1Osb>/Armc12<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	33536340
MGI:6513092	M	MP:0031012	impaired sperm migration in female genital tract	Armc12<em1Osb>/Armc12<em1Osb>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: C57BL/6NJcl * DBA/2NJcl	N	33536340
MGI:6513094	M	MP:0009237	kinked sperm flagellum	Armc12<em3Osb>/Armc12<em3Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	33536340
MGI:6513094	M	MP:0001925	male infertility	Armc12<em3Osb>/Armc12<em3Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	33536340
MGI:6513094	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Armc12<em3Osb>/Armc12<em3Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	33536340
MGI:6513095	M	MP:0009831	abnormal sperm midpiece morphology	Tbc1d21<em1Osb>/Tbc1d21<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	33536340
MGI:6513095	M	MP:0001925	male infertility	Tbc1d21<em1Osb>/Tbc1d21<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	33536340
MGI:6513095	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Tbc1d21<em1Osb>/Tbc1d21<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	33536340
MGI:6513095	M	MP:0006380	abnormal spermatid morphology	Tbc1d21<em1Osb>/Tbc1d21<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	33536340
MGI:6513140	M	MP:0001407	short stride length	Gnao1<em2Rneu>/Gnao1<+>	C57BL/6J-Gnao1<em2Rneu>	N	31907305
MGI:6513140	F	MP:0012106	impaired exercise endurance	Gnao1<em2Rneu>/Gnao1<+>	C57BL/6J-Gnao1<em2Rneu>	N	31907305
MGI:6513140	F	MP:0001413	abnormal response to new environment	Gnao1<em2Rneu>/Gnao1<+>	C57BL/6J-Gnao1<em2Rneu>	N	31907305
MGI:6513200	F	MP:0002773	decreased circulating luteinizing hormone level	Tacr2<tm1(KOMP)Wtsi>/Tacr2<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	33427049
MGI:6513200	M	MP:0005559	increased circulating glucose level	Tacr2<tm1(KOMP)Wtsi>/Tacr2<tm1(KOMP)Wtsi>	involves: C57BL/6N	N	33427049
MGI:6514396	M	MP:0001922	reduced male fertility	Slc25a28<tm1.2Dwrd>/Slc25a28<tm1.2Dwrd>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32518166
MGI:6514396	M	MP:0002687	oligozoospermia	Slc25a28<tm1.2Dwrd>/Slc25a28<tm1.2Dwrd>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32518166
MGI:6514396	M	MP:0002675	asthenozoospermia	Slc25a28<tm1.2Dwrd>/Slc25a28<tm1.2Dwrd>	involves: 129S6/SvEvTac * C57BL/6NCrl	N	32518166
MGI:6514718	M	MP:0005389	reproductive system phenotype	Golga4<em1Syu>/Golga4<em1Syu>	Not Specified	Y	32736686
MGI:6514742	M	MP:0031012	impaired sperm migration in female genital tract	Prss59<em1Fcw>/Prss59<em1Fcw>	involves: C57BL/6	N	32020604
MGI:6514742	M	MP:0000242	impaired fertilization	Prss59<em1Fcw>/Prss59<em1Fcw>	involves: C57BL/6	N	32020604
MGI:6514742	M	MP:0001925	male infertility	Prss59<em1Fcw>/Prss59<em1Fcw>	involves: C57BL/6	N	32020604
MGI:6514801	M	MP:0001325	abnormal retina morphology	Prickle3<em1Mxg>/Prickle3<em1Mxg>	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514801	M	MP:0008067	retina ganglion cell degeneration	Prickle3<em1Mxg>/Prickle3<em1Mxg>	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514801	M	MP:0004022	abnormal cone electrophysiology	Prickle3<em1Mxg>/Prickle3<em1Mxg>	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514801	M	MP:0004021	abnormal rod electrophysiology	Prickle3<em1Mxg>/Prickle3<em1Mxg>	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514802	F	MP:0031141	increased retina vascular tortuosity	Prickle3<em1Mxg>/Y	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514802	F	MP:0004021	abnormal rod electrophysiology	Prickle3<em1Mxg>/Y	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514802	F	MP:0004022	abnormal cone electrophysiology	Prickle3<em1Mxg>/Y	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514802	F	MP:0010097	abnormal retina blood vessel morphology	Prickle3<em1Mxg>/Y	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514802	F	MP:0020339	abnormal retina ganglion cell dendrite morphology	Prickle3<em1Mxg>/Y	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514802	F	MP:0006035	abnormal mitochondrial morphology	Prickle3<em1Mxg>/Y	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514802	F	MP:0008067	retina ganglion cell degeneration	Prickle3<em1Mxg>/Y	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514803	F	MP:0010097	abnormal retina blood vessel morphology	Prickle3<em1Mxg>/Prickle3<+>	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514803	F	MP:0020339	abnormal retina ganglion cell dendrite morphology	Prickle3<em1Mxg>/Prickle3<+>	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514803	F	MP:0006035	abnormal mitochondrial morphology	Prickle3<em1Mxg>/Prickle3<+>	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514803	F	MP:0001325	abnormal retina morphology	Prickle3<em1Mxg>/Prickle3<+>	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514803	F	MP:0031141	increased retina vascular tortuosity	Prickle3<em1Mxg>/Prickle3<+>	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514803	F	MP:0004022	abnormal cone electrophysiology	Prickle3<em1Mxg>/Prickle3<+>	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514803	F	MP:0004021	abnormal rod electrophysiology	Prickle3<em1Mxg>/Prickle3<+>	C57BL/6JSlacc-Prickle3<em1Mxg>	N	32516135
MGI:6514859	M	MP:0001925	male infertility	1700102P08Rik<em1Feis>/1700102P08Rik<em1Feis>	C57BL/6-1700102P08Rik<em1Feis>	N	31930642
MGI:6514859	M	MP:0004930	small epididymis	1700102P08Rik<em1Feis>/1700102P08Rik<em1Feis>	C57BL/6-1700102P08Rik<em1Feis>	N	31930642
MGI:6514859	M	MP:0008261	arrest of male meiosis	1700102P08Rik<em1Feis>/1700102P08Rik<em1Feis>	C57BL/6-1700102P08Rik<em1Feis>	N	31930642
MGI:6514859	M	MP:0014052	increased male germ cell apoptosis	1700102P08Rik<em1Feis>/1700102P08Rik<em1Feis>	C57BL/6-1700102P08Rik<em1Feis>	N	31930642
MGI:6514859	M	MP:0005159	azoospermia	1700102P08Rik<em1Feis>/1700102P08Rik<em1Feis>	C57BL/6-1700102P08Rik<em1Feis>	N	31930642
MGI:6514859	M	MP:0001147	small testis	1700102P08Rik<em1Feis>/1700102P08Rik<em1Feis>	C57BL/6-1700102P08Rik<em1Feis>	N	31930642
MGI:6514876	M	MP:0001861	lung inflammation	Ace2<em2(ACE2)Gpt>/Y	C57BL/6JGpt-Ace2<em2(ACE2)Gpt>/Gpt	N	MGI:6507771
MGI:6514876	M	MP:0010180	increased susceptibility to weight loss	Ace2<em2(ACE2)Gpt>/Y	C57BL/6JGpt-Ace2<em2(ACE2)Gpt>/Gpt	N	MGI:6507771
MGI:6514876	M	MP:0020949	increased susceptibility to Coronaviridae infection	Ace2<em2(ACE2)Gpt>/Y	C57BL/6JGpt-Ace2<em2(ACE2)Gpt>/Gpt	N	MGI:6507771
MGI:6515558	M	MP:0020451	decreased sperm progressive motility	Ttll3<tm1.2Ics>/Ttll3<tm1.2Ics>,Ttll8<tm1.2Ics>/Ttll8<tm1.2Ics>	B6.129S2-Ttll3<tm1.2Ics> Ttll8<tm1.2Ics>	N	33414192
MGI:6515558	M	MP:0009647	decreased fertilization frequency	Ttll3<tm1.2Ics>/Ttll3<tm1.2Ics>,Ttll8<tm1.2Ics>/Ttll8<tm1.2Ics>	B6.129S2-Ttll3<tm1.2Ics> Ttll8<tm1.2Ics>	N	33414192
MGI:6515558	M	MP:0002675	asthenozoospermia	Ttll3<tm1.2Ics>/Ttll3<tm1.2Ics>,Ttll8<tm1.2Ics>/Ttll8<tm1.2Ics>	B6.129S2-Ttll3<tm1.2Ics> Ttll8<tm1.2Ics>	N	33414192
MGI:6515558	M	MP:0001922	reduced male fertility	Ttll3<tm1.2Ics>/Ttll3<tm1.2Ics>,Ttll8<tm1.2Ics>/Ttll8<tm1.2Ics>	B6.129S2-Ttll3<tm1.2Ics> Ttll8<tm1.2Ics>	N	33414192
MGI:6515558	M	MP:0009237	kinked sperm flagellum	Ttll3<tm1.2Ics>/Ttll3<tm1.2Ics>,Ttll8<tm1.2Ics>/Ttll8<tm1.2Ics>	B6.129S2-Ttll3<tm1.2Ics> Ttll8<tm1.2Ics>	N	33414192
MGI:6515772	M	MP:0004852	decreased testis weight	Ssmem1<em1Osb>/Ssmem1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32301969
MGI:6515772	M	MP:0009230	abnormal sperm head morphology	Ssmem1<em1Osb>/Ssmem1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32301969
MGI:6515772	M	MP:0002675	asthenozoospermia	Ssmem1<em1Osb>/Ssmem1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32301969
MGI:6515772	M	MP:0002686	globozoospermia	Ssmem1<em1Osb>/Ssmem1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32301969
MGI:6515772	M	MP:0001147	small testis	Ssmem1<em1Osb>/Ssmem1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32301969
MGI:6515772	M	MP:0001925	male infertility	Ssmem1<em1Osb>/Ssmem1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32301969
MGI:6515772	M	MP:0001932	abnormal spermiogenesis	Ssmem1<em1Osb>/Ssmem1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32301969
MGI:6515831	M	MP:0002083	premature death	Ryr1<tm3.1Alle>/Ryr1<tm3.1Alle>	involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6	N	30236258
MGI:6678578	M	MP:0009142	decreased prepulse inhibition	Aplnr<tm1.1(KOMP)Vlcg>/Aplnr<+>	C57BL/6N-Aplnr<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6678752	F	MP:0005568	increased circulating total protein level	Dnah5<tm1b(KOMP)Wtsi>/Dnah5<+>	C57BL/6N-Dnah5<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6678752	F	MP:0000194	increased circulating calcium level	Dnah5<tm1b(KOMP)Wtsi>/Dnah5<+>	C57BL/6N-Dnah5<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6678752	F	MP:0005565	increased blood urea nitrogen level	Dnah5<tm1b(KOMP)Wtsi>/Dnah5<+>	C57BL/6N-Dnah5<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6678787	F	MP:0011960	abnormal eye anterior chamber depth	Erc1<tm1b(EUCOMM)Hmgu>/Erc1<+>	C57BL/6N-Erc1<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6678911	F	MP:0005561	increased mean corpuscular hemoglobin	Ipo8<tm1.1(KOMP)Vlcg>/Ipo8<+>	C57BL/6N-Ipo8<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6678948	F	MP:0005292	improved glucose tolerance	Lpar1<tm1b(EUCOMM)Wtsi>/Lpar1<+>	C57BL/6N-Lpar1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6678948	F	MP:0001304	cataract	Lpar1<tm1b(EUCOMM)Wtsi>/Lpar1<+>	C57BL/6N-Lpar1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6678948	F	MP:0013279	increased fasting circulating glucose level	Lpar1<tm1b(EUCOMM)Wtsi>/Lpar1<+>	C57BL/6N-Lpar1<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6678978	M	MP:0003917	increased kidney weight	Mid1ip1<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Mid1ip1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6679102	F	MP:0010053	decreased grip strength	Ppip5k2<tm1b(EUCOMM)Wtsi>/Ppip5k2<+>	C57BL/6N-Ppip5k2<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6679122	M	MP:0006243	impaired pupillary reflex	Ptcd3<tm1.1(KOMP)Vlcg>/Ptcd3<+>	C57BL/6N-Ptcd3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6679122	M	MP:0005561	increased mean corpuscular hemoglobin	Ptcd3<tm1.1(KOMP)Vlcg>/Ptcd3<+>	C57BL/6N-Ptcd3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6679122	M	MP:0000186	decreased circulating HDL cholesterol level	Ptcd3<tm1.1(KOMP)Vlcg>/Ptcd3<+>	C57BL/6N-Ptcd3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6679127	M	MP:0012362	increased large unstained cell number	Pts<tm1b(EUCOMM)Wtsi>/Pts<+>	C57BL/6N-Pts<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6679132	F	MP:0010124	decreased bone mineral content	Rab23<tm1b(EUCOMM)Wtsi>/Rab23<+>	C57BL/6N-Rab23<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6679132	F	MP:0003961	decreased lean body mass	Rab23<tm1b(EUCOMM)Wtsi>/Rab23<+>	C57BL/6N-Rab23<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6679132	M	MP:0002599	increased mean platelet volume	Rab23<tm1b(EUCOMM)Wtsi>/Rab23<+>	C57BL/6N-Rab23<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6679132	F	MP:0002941	increased circulating alanine transaminase level	Rab23<tm1b(EUCOMM)Wtsi>/Rab23<+>	C57BL/6N-Rab23<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6679132	F	MP:0005343	increased circulating aspartate transaminase level	Rab23<tm1b(EUCOMM)Wtsi>/Rab23<+>	C57BL/6N-Rab23<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6679143	M	MP:0000598	abnormal liver morphology	Rbm3<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Rbm3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6679190	M	MP:0010052	increased grip strength	Sfxn5<tm1b(EUCOMM)Hmgu>/Sfxn5<+>	C57BL/6N-Sfxn5<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6679190	M	MP:0013278	decreased fasting circulating glucose level	Sfxn5<tm1b(EUCOMM)Hmgu>/Sfxn5<+>	C57BL/6N-Sfxn5<tm1b(EUCOMM)Hmgu>/J	N	MGI:5576271
MGI:6679232	M	MP:0001399	hyperactivity	Snx18<tm1.1(KOMP)Vlcg>/Snx18<+>	C57BL/6N-Snx18<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6679255	F	MP:0001258	decreased body length	Sugt1<tm1b(KOMP)Wtsi>/Sugt1<+>	C57BL/6N-Sugt1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6679261	F	MP:0001102	small superior vagus ganglion	Taf8<tm2b(EUCOMM)Wtsi>/Taf8<+>	C57BL/6N-Taf8<tm2b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6679261	F	MP:0009709	hydrometra	Taf8<tm2b(EUCOMM)Wtsi>/Taf8<+>	C57BL/6N-Taf8<tm2b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:6679280	F	MP:0002968	increased circulating alkaline phosphatase level	Timm10b<tm1.1(KOMP)Vlcg>/Timm10b<+>	C57BL/6N-Timm10b<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6679300	F	MP:0004122	abnormal sinus arrhythmia	Tmtc3<tm1b(EUCOMM)Wtsi>/Tmtc3<+>	C57BL/6N-Tmtc3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6679300	F	MP:0003928	increased heart rate variability	Tmtc3<tm1b(EUCOMM)Wtsi>/Tmtc3<+>	C57BL/6N-Tmtc3<tm1b(EUCOMM)Wtsi>/Bay	N	MGI:5576271
MGI:6679313	M	MP:0000613	abnormal salivary gland morphology	Tomm6<tm1a(KOMP)Wtsi>/Tomm6<+>	C57BL/6N-Tomm6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6679313	M	MP:0000266	abnormal heart morphology	Tomm6<tm1a(KOMP)Wtsi>/Tomm6<+>	C57BL/6N-Tomm6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6679313	M	MP:0005343	increased circulating aspartate transaminase level	Tomm6<tm1a(KOMP)Wtsi>/Tomm6<+>	C57BL/6N-Tomm6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6679313	M	MP:0002339	abnormal lymph node morphology	Tomm6<tm1a(KOMP)Wtsi>/Tomm6<+>	C57BL/6N-Tomm6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6679313	M	MP:0000274	enlarged heart	Tomm6<tm1a(KOMP)Wtsi>/Tomm6<+>	C57BL/6N-Tomm6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6679313	M	MP:0000702	enlarged lymph nodes	Tomm6<tm1a(KOMP)Wtsi>/Tomm6<+>	C57BL/6N-Tomm6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6679313	M	MP:0011971	increased circulating lactate dehydrogenase level	Tomm6<tm1a(KOMP)Wtsi>/Tomm6<+>	C57BL/6N-Tomm6<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6679322	F	MP:0003731	abnormal retina outer nuclear layer morphology	Trim59<tm1b(EUCOMM)Hmgu>/Trim59<+>	C57BL/6N-Trim59<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6679323	M	MP:0001399	hyperactivity	Trp53bp2<tm1b(EUCOMM)Hmgu>/Trp53bp2<+>	C57BL/6N-Trp53bp2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6679323	M	MP:0005343	increased circulating aspartate transaminase level	Trp53bp2<tm1b(EUCOMM)Hmgu>/Trp53bp2<+>	C57BL/6N-Trp53bp2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6679323	M	MP:0005564	increased hemoglobin content	Trp53bp2<tm1b(EUCOMM)Hmgu>/Trp53bp2<+>	C57BL/6N-Trp53bp2<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6679353	F	MP:0010053	decreased grip strength	Xpnpep3<tm1.1(KOMP)Vlcg>/Xpnpep3<+>	C57BL/6N-Xpnpep3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6680967	M	MP:0002574	increased vertical activity	Klhdc7a<tm1.1(KOMP)Vlcg>/Klhdc7a<tm1.1(KOMP)Vlcg>	C57BL/6N-Klhdc7a<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6681844	M	MP:0006378	abnormal spermatogonia morphology	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681844	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681844	M	MP:0013272	abnormal translation	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681844	M	MP:0020362	abnormal male germ cell physiology	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681844	M	MP:0004901	decreased male germ cell number	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681844	M	MP:0001925	male infertility	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681844	M	MP:0001147	small testis	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681844	M	MP:0012167	abnormal epigenetic regulation of gene expression	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681844	M	MP:0006362	abnormal male germ cell morphology	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681845	M	MP:0012167	abnormal epigenetic regulation of gene expression	Mettl14<em1Chhe>/Mettl14<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681845	M	MP:0004901	decreased male germ cell number	Mettl14<em1Chhe>/Mettl14<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681845	M	MP:0001925	male infertility	Mettl14<em1Chhe>/Mettl14<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681845	M	MP:0001147	small testis	Mettl14<em1Chhe>/Mettl14<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681845	M	MP:0006378	abnormal spermatogonia morphology	Mettl14<em1Chhe>/Mettl14<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681845	M	MP:0013272	abnormal translation	Mettl14<em1Chhe>/Mettl14<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681845	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Mettl14<em1Chhe>/Mettl14<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681848	M	MP:0006378	abnormal spermatogonia morphology	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681848	M	MP:0004901	decreased male germ cell number	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	28914256
MGI:6681851	M	MP:0005389	reproductive system phenotype	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	Y	28914256
MGI:6681851	M	MP:0012167	abnormal epigenetic regulation of gene expression	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681852	M	MP:0005389	reproductive system phenotype	Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	Y	28914256
MGI:6681852	M	MP:0012167	abnormal epigenetic regulation of gene expression	Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681853	M	MP:0020451	decreased sperm progressive motility	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681853	M	MP:0004852	decreased testis weight	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681853	M	MP:0012167	abnormal epigenetic regulation of gene expression	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681853	M	MP:0002216	abnormal seminiferous tubule morphology	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681853	M	MP:0001147	small testis	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681853	M	MP:0005578	teratozoospermia	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681853	M	MP:0002675	asthenozoospermia	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681853	M	MP:0006380	abnormal spermatid morphology	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681853	M	MP:0002687	oligozoospermia	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681853	M	MP:0008279	arrest of spermiogenesis	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681853	M	MP:0013272	abnormal translation	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681853	M	MP:0009230	abnormal sperm head morphology	Mettl3<em1Chhe>/Mettl3<em1Chhe>,Mettl14<em1Chhe>/Mettl14<em1Chhe>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6J	N	28914256
MGI:6681929	M	MP:0001925	male infertility	Pmfbp1<em#Jfw>/Pmfbp1<em#Jfw>	Not Specified	N	30298696
MGI:6681929	M	MP:0009234	absent sperm head	Pmfbp1<em#Jfw>/Pmfbp1<em#Jfw>	Not Specified	N	30298696
MGI:6681929	M	MP:0009838	abnormal sperm axoneme morphology	Pmfbp1<em#Jfw>/Pmfbp1<em#Jfw>	Not Specified	N	30298696
MGI:6681929	M	MP:0014468	disorganized sperm mitochondrial sheath	Pmfbp1<em#Jfw>/Pmfbp1<em#Jfw>	Not Specified	N	30298696
MGI:6682156	F	MP:0001523	impaired righting response	Fgf7<tm1e.1(EUCOMM)Hmgu>/Fgf7<tm1e.1(EUCOMM)Hmgu>	C57BL/6N-Fgf7<tm1e.1(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6682156	M	MP:0002546	mydriasis	Fgf7<tm1e.1(EUCOMM)Hmgu>/Fgf7<tm1e.1(EUCOMM)Hmgu>	C57BL/6N-Fgf7<tm1e.1(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6682156	M	MP:0001486	abnormal startle reflex	Fgf7<tm1e.1(EUCOMM)Hmgu>/Fgf7<tm1e.1(EUCOMM)Hmgu>	C57BL/6N-Fgf7<tm1e.1(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6682156	M	MP:0001319	irregularly shaped pupil	Fgf7<tm1e.1(EUCOMM)Hmgu>/Fgf7<tm1e.1(EUCOMM)Hmgu>	C57BL/6N-Fgf7<tm1e.1(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6682156	M	MP:0001322	abnormal iris morphology	Fgf7<tm1e.1(EUCOMM)Hmgu>/Fgf7<tm1e.1(EUCOMM)Hmgu>	C57BL/6N-Fgf7<tm1e.1(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6682156	M	MP:0006241	abnormal placement of pupils	Fgf7<tm1e.1(EUCOMM)Hmgu>/Fgf7<tm1e.1(EUCOMM)Hmgu>	C57BL/6N-Fgf7<tm1e.1(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6682156	M	MP:0006243	impaired pupillary reflex	Fgf7<tm1e.1(EUCOMM)Hmgu>/Fgf7<tm1e.1(EUCOMM)Hmgu>	C57BL/6N-Fgf7<tm1e.1(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6682158	M	MP:0000745	tremors	Nat8f5<tm1b(EUCOMM)Wtsi>/Nat8f5<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cml5<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6682159	F	MP:0002060	abnormal skin morphology	Nexmif<em1(IMPC)Tcp>/Nexmif<+>	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6682159	F	MP:0001399	hyperactivity	Nexmif<em1(IMPC)Tcp>/Nexmif<+>	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6682159	F	MP:0000157	abnormal sternum morphology	Nexmif<em1(IMPC)Tcp>/Nexmif<+>	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6682159	F	MP:0000219	increased neutrophil cell number	Nexmif<em1(IMPC)Tcp>/Nexmif<+>	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6682159	F	MP:0002989	small kidney	Nexmif<em1(IMPC)Tcp>/Nexmif<+>	C57BL/6N-Nexmif<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6682160	F	MP:0020421	increased freezing behavior	Nkapd1<em1(IMPC)Mbp>/Nkapd1<+>	C57BL/6N-Nkapd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6682160	F	MP:0002135	abnormal kidney morphology	Nkapd1<em1(IMPC)Mbp>/Nkapd1<+>	C57BL/6N-Nkapd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6682160	F	MP:0009142	decreased prepulse inhibition	Nkapd1<em1(IMPC)Mbp>/Nkapd1<+>	C57BL/6N-Nkapd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6682160	F	MP:0002989	small kidney	Nkapd1<em1(IMPC)Mbp>/Nkapd1<+>	C57BL/6N-Nkapd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6682161	M	MP:0001510	abnormal coat appearance	Pgm1<em1(IMPC)J>/Pgm1<+>	C57BL/6NJ-Pgm1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6682161	M	MP:0000367	abnormal coat/ hair morphology	Pgm1<em1(IMPC)J>/Pgm1<+>	C57BL/6NJ-Pgm1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6682163	F	MP:0011100	preweaning lethality, complete penetrance	Robo4<tm1.1(KOMP)Vlcg>/Robo4<tm1.1(KOMP)Vlcg>	C57BL/6N-Robo4<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6690320	M	MP:0005376	homeostasis/metabolism phenotype	Jazf1<tm1c(EUCOMM)Wtsi>/Jazf1<tm1c(EUCOMM)Wtsi>,Tg(Ins2-cre)23Herr/0	involves: 129S4/SvJaeSor * C57BL/6N * CBA/J	Y	32640216
MGI:6690320	M	MP:0009114	decreased pancreatic beta cell mass	Jazf1<tm1c(EUCOMM)Wtsi>/Jazf1<tm1c(EUCOMM)Wtsi>,Tg(Ins2-cre)23Herr/0	involves: 129S4/SvJaeSor * C57BL/6N * CBA/J	N	32640216
MGI:6690320	M	MP:0005379	endocrine/exocrine gland phenotype	Jazf1<tm1c(EUCOMM)Wtsi>/Jazf1<tm1c(EUCOMM)Wtsi>,Tg(Ins2-cre)23Herr/0	involves: 129S4/SvJaeSor * C57BL/6N * CBA/J	Y	32640216
MGI:6690320	M	MP:0005378	growth/size/body region phenotype	Jazf1<tm1c(EUCOMM)Wtsi>/Jazf1<tm1c(EUCOMM)Wtsi>,Tg(Ins2-cre)23Herr/0	involves: 129S4/SvJaeSor * C57BL/6N * CBA/J	Y	32640216
MGI:6690320	M	MP:0010147	abnormal endocrine pancreas physiology	Jazf1<tm1c(EUCOMM)Wtsi>/Jazf1<tm1c(EUCOMM)Wtsi>,Tg(Ins2-cre)23Herr/0	involves: 129S4/SvJaeSor * C57BL/6N * CBA/J	N	32640216
MGI:6690320	M	MP:0013272	abnormal translation	Jazf1<tm1c(EUCOMM)Wtsi>/Jazf1<tm1c(EUCOMM)Wtsi>,Tg(Ins2-cre)23Herr/0	involves: 129S4/SvJaeSor * C57BL/6N * CBA/J	N	32640216
MGI:6690603	M	MP:0001925	male infertility	Phf7<tm1c(EUCOMM)Hmgu>/Phf7<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	32726616
MGI:6690603	M	MP:0009232	abnormal sperm nucleus morphology	Phf7<tm1c(EUCOMM)Hmgu>/Phf7<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	32726616
MGI:6690603	M	MP:0009233	enlarged sperm head	Phf7<tm1c(EUCOMM)Hmgu>/Phf7<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	32726616
MGI:6690603	M	MP:0009647	decreased fertilization frequency	Phf7<tm1c(EUCOMM)Hmgu>/Phf7<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	32726616
MGI:6690603	M	MP:0009230	abnormal sperm head morphology	Phf7<tm1c(EUCOMM)Hmgu>/Phf7<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	32726616
MGI:6690603	M	MP:0002687	oligozoospermia	Phf7<tm1c(EUCOMM)Hmgu>/Phf7<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	32726616
MGI:6690603	M	MP:0002686	globozoospermia	Phf7<tm1c(EUCOMM)Hmgu>/Phf7<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	32726616
MGI:6690603	M	MP:0002675	asthenozoospermia	Phf7<tm1c(EUCOMM)Hmgu>/Phf7<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	32726616
MGI:6690604	M	MP:0009232	abnormal sperm nucleus morphology	Phf7<em2Osb>/Phf7<em2Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/0	involves: 129S2/SvPas * C57BL/6NSlc	N	32726616
MGI:6690604	M	MP:0005578	teratozoospermia	Phf7<em2Osb>/Phf7<em2Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/0	involves: 129S2/SvPas * C57BL/6NSlc	N	32726616
MGI:6690604	M	MP:0002675	asthenozoospermia	Phf7<em2Osb>/Phf7<em2Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/0	involves: 129S2/SvPas * C57BL/6NSlc	N	32726616
MGI:6690604	M	MP:0001925	male infertility	Phf7<em2Osb>/Phf7<em2Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/0	involves: 129S2/SvPas * C57BL/6NSlc	N	32726616
MGI:6690604	M	MP:0009647	decreased fertilization frequency	Phf7<em2Osb>/Phf7<em2Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/0	involves: 129S2/SvPas * C57BL/6NSlc	N	32726616
MGI:6690604	M	MP:0002687	oligozoospermia	Phf7<em2Osb>/Phf7<em2Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/0	involves: 129S2/SvPas * C57BL/6NSlc	N	32726616
MGI:6690698	M	MP:0003961	decreased lean body mass	Dhcr7<tm1.1Sbpa>/Dhcr7<tm1.1Sbpa>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	B6.Cg-Dhcr7<tm1.1Sbpa> Speer6-ps1<Tg(Alb-cre)21Mgn>	N	33410752
MGI:6690698	M	MP:0004789	increased bile salt level	Dhcr7<tm1.1Sbpa>/Dhcr7<tm1.1Sbpa>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	B6.Cg-Dhcr7<tm1.1Sbpa> Speer6-ps1<Tg(Alb-cre)21Mgn>	N	33410752
MGI:6690855	F	MP:0001926	female infertility	Mcidas<em1Sroy>/Mcidas<em1Sroy>	C57BL/6-Mcidas<em1Sroy>	N	30877126
MGI:6690855	M	MP:0001925	male infertility	Mcidas<em1Sroy>/Mcidas<em1Sroy>	C57BL/6-Mcidas<em1Sroy>	N	30877126
MGI:6690855	F	MP:0011644	abnormal oviduct epithelium motile cilium morphology	Mcidas<em1Sroy>/Mcidas<em1Sroy>	C57BL/6-Mcidas<em1Sroy>	N	30877126
MGI:6690894	M	MP:0003631	nervous system phenotype	Tmem74<em1Fehan>/Tmem74<em1Fehan>	C57BL/6-Tmem74<em1Fehan>	Y	30886335
MGI:6693343	F	MP:0001926	female infertility	Pabpn1l<em1Hyfn>/Pabpn1l<em1Hyfn>	C57BL/6-Pabpn1l<em1Hyfn>	N	32558204
MGI:6693343	F	MP:0001125	abnormal oocyte morphology	Pabpn1l<em1Hyfn>/Pabpn1l<em1Hyfn>	C57BL/6-Pabpn1l<em1Hyfn>	N	32558204
MGI:6693343	M	MP:0005389	reproductive system phenotype	Pabpn1l<em1Hyfn>/Pabpn1l<em1Hyfn>	C57BL/6-Pabpn1l<em1Hyfn>	Y	32558204
MGI:6693343	F	MP:0003718	maternal effect	Pabpn1l<em1Hyfn>/Pabpn1l<em1Hyfn>	C57BL/6-Pabpn1l<em1Hyfn>	N	32558204
MGI:6693346	M	MP:0005389	reproductive system phenotype	Nemp1<em1Hmc>/Nemp1<em1Hmc>	C57BL/6N-Nemp1<em1Hmc>	Y	32923640
MGI:6693346	F	MP:0001926	female infertility	Nemp1<em1Hmc>/Nemp1<em1Hmc>	C57BL/6N-Nemp1<em1Hmc>	N	32923640
MGI:6693346	F	MP:0001125	abnormal oocyte morphology	Nemp1<em1Hmc>/Nemp1<em1Hmc>	C57BL/6N-Nemp1<em1Hmc>	N	32923640
MGI:6693346	F	MP:0001923	reduced female fertility	Nemp1<em1Hmc>/Nemp1<em1Hmc>	C57BL/6N-Nemp1<em1Hmc>	N	32923640
MGI:6693346	F	MP:0005168	abnormal female meiosis	Nemp1<em1Hmc>/Nemp1<em1Hmc>	C57BL/6N-Nemp1<em1Hmc>	N	32923640
MGI:6693346	F	MP:0003718	maternal effect	Nemp1<em1Hmc>/Nemp1<em1Hmc>	C57BL/6N-Nemp1<em1Hmc>	N	32923640
MGI:6693346	F	MP:0011121	decreased primordial ovarian follicle number	Nemp1<em1Hmc>/Nemp1<em1Hmc>	C57BL/6N-Nemp1<em1Hmc>	N	32923640
MGI:6693353	M	MP:0008898	abnormal acrosome morphology	Actl9<em1Glin>/Actl9<em1Glin>	involves: C57BL/6J	N	33626338
MGI:6693353	M	MP:0009231	detached acrosome	Actl9<em1Glin>/Actl9<em1Glin>	involves: C57BL/6J	N	33626338
MGI:6693353	M	MP:0031354	abnormal acrosome assembly	Actl9<em1Glin>/Actl9<em1Glin>	involves: C57BL/6J	N	33626338
MGI:6693353	M	MP:0031355	abnormal proacrosomal vesicle fusion	Actl9<em1Glin>/Actl9<em1Glin>	involves: C57BL/6J	N	33626338
MGI:6693353	M	MP:0006380	abnormal spermatid morphology	Actl9<em1Glin>/Actl9<em1Glin>	involves: C57BL/6J	N	33626338
MGI:6693353	M	MP:0000242	impaired fertilization	Actl9<em1Glin>/Actl9<em1Glin>	involves: C57BL/6J	N	33626338
MGI:6693475	M	MP:0010959	abnormal oxidative phosphorylation	Bud23<em1Asil>/Bud23<+>	involves: C57BL/6 * DBA/2	N	31939735
MGI:6693495	F	MP:0011094	embryonic lethality before implantation, complete penetrance	Zrsr2-ps1<em1Alfon>/Zrsr2-ps1<+>,Zrsr2<em1Alfon>/Zrsr2<+>	involves: C57BL/6 * CBA	N	32527007
MGI:6693496	M	MP:0011094	embryonic lethality before implantation, complete penetrance	Zrsr2-ps1<em1Alfon>/Zrsr2-ps1<+>,Zrsr2<em1Alfon>/Y	involves: C57BL/6 * CBA	N	32527007
MGI:6693526	M	MP:0009288	increased epididymal fat pad weight	Fhip2b<em1Wwan>/Fhip2b<em1Wwan>	involves: C57BL/6	N	32289885
MGI:6693621	M	MP:0001750	increased circulating follicle stimulating hormone level	Csnk1g2<em1Xidw>/Csnk1g2<em1Xidw>	Not Specified	N	33206046
MGI:6693621	M	MP:0005416	abnormal circulating protein level	Csnk1g2<em1Xidw>/Csnk1g2<em1Xidw>	Not Specified	N	33206046
MGI:6693621	M	MP:0002780	decreased circulating testosterone level	Csnk1g2<em1Xidw>/Csnk1g2<em1Xidw>	Not Specified	N	33206046
MGI:6693621	M	MP:0004852	decreased testis weight	Csnk1g2<em1Xidw>/Csnk1g2<em1Xidw>	Not Specified	N	33206046
MGI:6693621	M	MP:0004909	increased seminal vesicle weight	Csnk1g2<em1Xidw>/Csnk1g2<em1Xidw>	Not Specified	N	33206046
MGI:6693621	M	MP:0001147	small testis	Csnk1g2<em1Xidw>/Csnk1g2<em1Xidw>	Not Specified	N	33206046
MGI:6693621	M	MP:0001751	increased circulating luteinizing hormone level	Csnk1g2<em1Xidw>/Csnk1g2<em1Xidw>	Not Specified	N	33206046
MGI:6693621	M	MP:0008995	early reproductive senescence	Csnk1g2<em1Xidw>/Csnk1g2<em1Xidw>	Not Specified	N	33206046
MGI:6693621	M	MP:0002216	abnormal seminiferous tubule morphology	Csnk1g2<em1Xidw>/Csnk1g2<em1Xidw>	Not Specified	N	33206046
MGI:6693621	M	MP:0001260	increased body weight	Csnk1g2<em1Xidw>/Csnk1g2<em1Xidw>	Not Specified	N	33206046
MGI:6693623	M	MP:0005376	homeostasis/metabolism phenotype	Csnk1g2<em1Xidw>/Csnk1g2<em1Xidw>,Ripk3<tm1Xidw>/Ripk3<tm1Xidw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	Y	33206046
MGI:6693623	M	MP:0005389	reproductive system phenotype	Csnk1g2<em1Xidw>/Csnk1g2<em1Xidw>,Ripk3<tm1Xidw>/Ripk3<tm1Xidw>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	Y	33206046
MGI:6693629	M	MP:0001925	male infertility	Foxj2<tm1.1Mxc>/Foxj2<tm1.1Mxc>,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	27316861
MGI:6693629	M	MP:0004852	decreased testis weight	Foxj2<tm1.1Mxc>/Foxj2<tm1.1Mxc>,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	27316861
MGI:6693629	M	MP:0009451	abnormal chromosomal synapsis	Foxj2<tm1.1Mxc>/Foxj2<tm1.1Mxc>,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	27316861
MGI:6693629	M	MP:0008261	arrest of male meiosis	Foxj2<tm1.1Mxc>/Foxj2<tm1.1Mxc>,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	27316861
MGI:6693629	F	MP:0005389	reproductive system phenotype	Foxj2<tm1.1Mxc>/Foxj2<tm1.1Mxc>,Tg(Ddx4-cre)1Dcas/0	involves: FVB	Y	27316861
MGI:6693638	M	MP:0001147	small testis	Spmip7<tm1Itl>/Spmip7<tm1Itl>	involves: C57BL/6J	N	29700843
MGI:6693638	M	MP:0004852	decreased testis weight	Spmip7<tm1Itl>/Spmip7<tm1Itl>	involves: C57BL/6J	N	29700843
MGI:6693638	M	MP:0005159	azoospermia	Spmip7<tm1Itl>/Spmip7<tm1Itl>	involves: C57BL/6J	N	29700843
MGI:6693647	F	MP:0005389	reproductive system phenotype	Tmem150b<em1Cya>/Tmem150b<em1Cya>	involves: C57BL/6J * ICR	Y	33288838
MGI:6693649	M	MP:0009376	abnormal manchette morphology	Sun3<em1Qsh>/Sun3<em1Qsh>	Not Specified	N	32156700
MGI:6693649	M	MP:0014052	increased male germ cell apoptosis	Sun3<em1Qsh>/Sun3<em1Qsh>	Not Specified	N	32156700
MGI:6693649	M	MP:0002686	globozoospermia	Sun3<em1Qsh>/Sun3<em1Qsh>	Not Specified	N	32156700
MGI:6693649	M	MP:0001147	small testis	Sun3<em1Qsh>/Sun3<em1Qsh>	Not Specified	N	32156700
MGI:6693649	F	MP:0005389	reproductive system phenotype	Sun3<em1Qsh>/Sun3<em1Qsh>	Not Specified	Y	32156700
MGI:6693649	M	MP:0001925	male infertility	Sun3<em1Qsh>/Sun3<em1Qsh>	Not Specified	N	32156700
MGI:6693649	M	MP:0002687	oligozoospermia	Sun3<em1Qsh>/Sun3<em1Qsh>	Not Specified	N	32156700
MGI:6693649	M	MP:0009831	abnormal sperm midpiece morphology	Sun3<em1Qsh>/Sun3<em1Qsh>	Not Specified	N	32156700
MGI:6693753	M	MP:0001925	male infertility	Del(2Spint4-Spint5)1Zuk/Del(2Spint4-Spint5)1Zuk	involves: C57BL/6 * DBA/2	N	32814578
MGI:6693753	M	MP:0001922	reduced male fertility	Del(2Spint4-Spint5)1Zuk/Del(2Spint4-Spint5)1Zuk	involves: C57BL/6 * DBA/2	N	32814578
MGI:6693753	M	MP:0001935	decreased litter size	Del(2Spint4-Spint5)1Zuk/Del(2Spint4-Spint5)1Zuk	involves: C57BL/6 * DBA/2	N	32814578
MGI:6693753	M	MP:0005389	reproductive system phenotype	Del(2Spint4-Spint5)1Zuk/Del(2Spint4-Spint5)1Zuk	involves: C57BL/6 * DBA/2	Y	32814578
MGI:6693754	M	MP:0002675	asthenozoospermia	Ces5a<em1Zuk>/Ces5a<em1Zuk>	involves: C57BL/6 * DBA/2	N	32814578
MGI:6693754	M	MP:0002687	oligozoospermia	Ces5a<em1Zuk>/Ces5a<em1Zuk>	involves: C57BL/6 * DBA/2	N	32814578
MGI:6693754	M	MP:0001922	reduced male fertility	Ces5a<em1Zuk>/Ces5a<em1Zuk>	involves: C57BL/6 * DBA/2	N	32814578
MGI:6693754	M	MP:0020451	decreased sperm progressive motility	Ces5a<em1Zuk>/Ces5a<em1Zuk>	involves: C57BL/6 * DBA/2	N	32814578
MGI:6693754	M	MP:0002631	abnormal epididymis morphology	Ces5a<em1Zuk>/Ces5a<em1Zuk>	involves: C57BL/6 * DBA/2	N	32814578
MGI:6693754	M	MP:0005389	reproductive system phenotype	Ces5a<em1Zuk>/Ces5a<em1Zuk>	involves: C57BL/6 * DBA/2	Y	32814578
MGI:6693762	M	MP:0005389	reproductive system phenotype	Laidx<em1.1Jbmu>/Y	B6.Cg-Laidx<em1.1Jbmu>	Y	32253194
MGI:6693763	F	MP:0005389	reproductive system phenotype	Laidx<em1.1Jbmu>/Laidx<em1.1Jbmu>	B6.Cg-Laidx<em1.1Jbmu>	Y	32253194
MGI:6693765	M	MP:0005389	reproductive system phenotype	Laidx<em1.2Jbmu>/Y	B6(FVB)-Laidx<em1.2Jbmu>	Y	32253194
MGI:6693828	M	MP:0001925	male infertility	Rimklb<em1Matak>/Rimklb<em1Matak>	C57BL/6J-Rimklb<em1Matak>	N	33633267
MGI:6693828	M	MP:0002216	abnormal seminiferous tubule morphology	Rimklb<em1Matak>/Rimklb<em1Matak>	C57BL/6J-Rimklb<em1Matak>	N	33633267
MGI:6693828	M	MP:0009230	abnormal sperm head morphology	Rimklb<em1Matak>/Rimklb<em1Matak>	C57BL/6J-Rimklb<em1Matak>	N	33633267
MGI:6693828	M	MP:0002675	asthenozoospermia	Rimklb<em1Matak>/Rimklb<em1Matak>	C57BL/6J-Rimklb<em1Matak>	N	33633267
MGI:6693828	M	MP:0000242	impaired fertilization	Rimklb<em1Matak>/Rimklb<em1Matak>	C57BL/6J-Rimklb<em1Matak>	N	33633267
MGI:6693828	M	MP:0002687	oligozoospermia	Rimklb<em1Matak>/Rimklb<em1Matak>	C57BL/6J-Rimklb<em1Matak>	N	33633267
MGI:6693828	M	MP:0001156	abnormal spermatogenesis	Rimklb<em1Matak>/Rimklb<em1Matak>	C57BL/6J-Rimklb<em1Matak>	N	33633267
MGI:6693828	M	MP:0004852	decreased testis weight	Rimklb<em1Matak>/Rimklb<em1Matak>	C57BL/6J-Rimklb<em1Matak>	N	33633267
MGI:6694136	M	MP:0004901	decreased male germ cell number	Cdc14a<em1Jgao>/Cdc14a<em1Jgao>	CBA/CaJ-Cdc14a<em1Jgao>	N	32679235
MGI:6694136	M	MP:0008261	arrest of male meiosis	Cdc14a<em1Jgao>/Cdc14a<em1Jgao>	CBA/CaJ-Cdc14a<em1Jgao>	N	32679235
MGI:6694136	M	MP:0005578	teratozoospermia	Cdc14a<em1Jgao>/Cdc14a<em1Jgao>	CBA/CaJ-Cdc14a<em1Jgao>	N	32679235
MGI:6694136	M	MP:0009234	absent sperm head	Cdc14a<em1Jgao>/Cdc14a<em1Jgao>	CBA/CaJ-Cdc14a<em1Jgao>	N	32679235
MGI:6694136	M	MP:0001922	reduced male fertility	Cdc14a<em1Jgao>/Cdc14a<em1Jgao>	CBA/CaJ-Cdc14a<em1Jgao>	N	32679235
MGI:6694136	M	MP:0009238	coiled sperm flagellum	Cdc14a<em1Jgao>/Cdc14a<em1Jgao>	CBA/CaJ-Cdc14a<em1Jgao>	N	32679235
MGI:6694136	M	MP:0009230	abnormal sperm head morphology	Cdc14a<em1Jgao>/Cdc14a<em1Jgao>	CBA/CaJ-Cdc14a<em1Jgao>	N	32679235
MGI:6694136	M	MP:0002675	asthenozoospermia	Cdc14a<em1Jgao>/Cdc14a<em1Jgao>	CBA/CaJ-Cdc14a<em1Jgao>	N	32679235
MGI:6694136	F	MP:0005389	reproductive system phenotype	Cdc14a<em1Jgao>/Cdc14a<em1Jgao>	CBA/CaJ-Cdc14a<em1Jgao>	Y	32679235
MGI:6694136	M	MP:0009232	abnormal sperm nucleus morphology	Cdc14a<em1Jgao>/Cdc14a<em1Jgao>	CBA/CaJ-Cdc14a<em1Jgao>	N	32679235
MGI:6694136	M	MP:0020451	decreased sperm progressive motility	Cdc14a<em1Jgao>/Cdc14a<em1Jgao>	CBA/CaJ-Cdc14a<em1Jgao>	N	32679235
MGI:6694136	M	MP:0010723	paternal effect	Cdc14a<em1Jgao>/Cdc14a<em1Jgao>	CBA/CaJ-Cdc14a<em1Jgao>	N	32679235
MGI:6694857	M	MP:0001154	seminiferous tubule degeneration	Cdc14a<tm1a(EUCOMM)Hmgu>/Cdc14a<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	N	29293958
MGI:6694857	M	MP:0005578	teratozoospermia	Cdc14a<tm1a(EUCOMM)Hmgu>/Cdc14a<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	N	29293958
MGI:6694857	M	MP:0002687	oligozoospermia	Cdc14a<tm1a(EUCOMM)Hmgu>/Cdc14a<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	N	29293958
MGI:6694857	M	MP:0001925	male infertility	Cdc14a<tm1a(EUCOMM)Hmgu>/Cdc14a<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	N	29293958
MGI:6694858	F	MP:0005389	reproductive system phenotype	Cdc14a<tm1b(EUCOMM)Hmgu>/Cdc14a<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	Y	29293958
MGI:6694858	M	MP:0005578	teratozoospermia	Cdc14a<tm1b(EUCOMM)Hmgu>/Cdc14a<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	N	29293958
MGI:6694858	M	MP:0001925	male infertility	Cdc14a<tm1b(EUCOMM)Hmgu>/Cdc14a<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	N	29293958
MGI:6694858	M	MP:0002687	oligozoospermia	Cdc14a<tm1b(EUCOMM)Hmgu>/Cdc14a<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	N	29293958
MGI:6694858	M	MP:0001154	seminiferous tubule degeneration	Cdc14a<tm1b(EUCOMM)Hmgu>/Cdc14a<tm1b(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	N	29293958
MGI:6694866	F	MP:0004047	abnormal milk composition	Sprn<em1Jvt>/Sprn<em1Jvt>	FVB/NJ-Sprn<em1Jvt>	N	32317725
MGI:6694866	F	MP:0003718	maternal effect	Sprn<em1Jvt>/Sprn<em1Jvt>	FVB/NJ-Sprn<em1Jvt>	N	32317725
MGI:6694866	F	MP:0001881	abnormal mammary gland physiology	Sprn<em1Jvt>/Sprn<em1Jvt>	FVB/NJ-Sprn<em1Jvt>	N	32317725
MGI:6694866	F	MP:0010174	decreased mammary gland epithelial cell proliferation	Sprn<em1Jvt>/Sprn<em1Jvt>	FVB/NJ-Sprn<em1Jvt>	N	32317725
MGI:6694866	F	MP:0001882	abnormal lactation	Sprn<em1Jvt>/Sprn<em1Jvt>	FVB/NJ-Sprn<em1Jvt>	N	32317725
MGI:6694866	F	MP:0000628	abnormal mammary gland development	Sprn<em1Jvt>/Sprn<em1Jvt>	FVB/NJ-Sprn<em1Jvt>	N	32317725
MGI:6694867	M	MP:0005578	teratozoospermia	Cdc14a<tm1d(EUCOMM)Hmgu>/Cdc14a<tm1d(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	N	29293958
MGI:6694867	M	MP:0002687	oligozoospermia	Cdc14a<tm1d(EUCOMM)Hmgu>/Cdc14a<tm1d(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	N	29293958
MGI:6694867	M	MP:0001154	seminiferous tubule degeneration	Cdc14a<tm1d(EUCOMM)Hmgu>/Cdc14a<tm1d(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	N	29293958
MGI:6694867	M	MP:0001925	male infertility	Cdc14a<tm1d(EUCOMM)Hmgu>/Cdc14a<tm1d(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	N	29293958
MGI:6694867	F	MP:0005389	reproductive system phenotype	Cdc14a<tm1d(EUCOMM)Hmgu>/Cdc14a<tm1d(EUCOMM)Hmgu>	involves: C57BL/6N * FVB	Y	29293958
MGI:6694869	M	MP:0002687	oligozoospermia	Cdc14a<em1Tbf>/Cdc14a<em1Tbf>	involves: C57BL/6J	N	29293958
MGI:6694869	M	MP:0001925	male infertility	Cdc14a<em1Tbf>/Cdc14a<em1Tbf>	involves: C57BL/6J	N	29293958
MGI:6694869	M	MP:0001154	seminiferous tubule degeneration	Cdc14a<em1Tbf>/Cdc14a<em1Tbf>	involves: C57BL/6J	N	29293958
MGI:6694878	M	MP:0002675	asthenozoospermia	Cabs1<em1Ntu>/Cabs1<em1Ntu>	C57BL/6-Cabs1<em1Ntu>	N	33440775
MGI:6694878	M	MP:0001922	reduced male fertility	Cabs1<em1Ntu>/Cabs1<em1Ntu>	C57BL/6-Cabs1<em1Ntu>	N	33440775
MGI:6694878	M	MP:0009835	absent sperm annulus	Cabs1<em1Ntu>/Cabs1<em1Ntu>	C57BL/6-Cabs1<em1Ntu>	N	33440775
MGI:6694878	M	MP:0009834	abnormal sperm annulus morphology	Cabs1<em1Ntu>/Cabs1<em1Ntu>	C57BL/6-Cabs1<em1Ntu>	N	33440775
MGI:6694878	M	MP:0009237	kinked sperm flagellum	Cabs1<em1Ntu>/Cabs1<em1Ntu>	C57BL/6-Cabs1<em1Ntu>	N	33440775
MGI:6694948	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Eaf1<tm1.1Zhow>/Eaf1<tm1.1Zhow>,Tg(Pbsn-cre)4Prb/0	B6(Cg)-Eaf1<tm1.1Zhow> Tg(Pbsn-cre)4Prb	N	31229879
MGI:6694948	M	MP:0003607	abnormal prostate gland physiology	Eaf1<tm1.1Zhow>/Eaf1<tm1.1Zhow>,Tg(Pbsn-cre)4Prb/0	B6(Cg)-Eaf1<tm1.1Zhow> Tg(Pbsn-cre)4Prb	N	31229879
MGI:6694948	M	MP:0005389	reproductive system phenotype	Eaf1<tm1.1Zhow>/Eaf1<tm1.1Zhow>,Tg(Pbsn-cre)4Prb/0	B6(Cg)-Eaf1<tm1.1Zhow> Tg(Pbsn-cre)4Prb	Y	31229879
MGI:6694948	M	MP:0003608	prostate gland inflammation	Eaf1<tm1.1Zhow>/Eaf1<tm1.1Zhow>,Tg(Pbsn-cre)4Prb/0	B6(Cg)-Eaf1<tm1.1Zhow> Tg(Pbsn-cre)4Prb	N	31229879
MGI:6694951	M	MP:0003608	prostate gland inflammation	Eaf2<tm1Zhow>/Eaf2<tm1Zhow>	involves: 129P2/OlaHsd	N	31229879
MGI:6694951	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Eaf2<tm1Zhow>/Eaf2<tm1Zhow>	involves: 129P2/OlaHsd	N	31229879
MGI:6694951	M	MP:0003607	abnormal prostate gland physiology	Eaf2<tm1Zhow>/Eaf2<tm1Zhow>	involves: 129P2/OlaHsd	N	31229879
MGI:6694954	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Eaf1<tm1.1Zhow>/Eaf1<tm1.1Zhow>,Eaf2<tm1Zhow>/Eaf2<tm1Zhow>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * DBA/2	N	31229879
MGI:6694954	M	MP:0003608	prostate gland inflammation	Eaf1<tm1.1Zhow>/Eaf1<tm1.1Zhow>,Eaf2<tm1Zhow>/Eaf2<tm1Zhow>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * DBA/2	N	31229879
MGI:6694954	M	MP:0003607	abnormal prostate gland physiology	Eaf1<tm1.1Zhow>/Eaf1<tm1.1Zhow>,Eaf2<tm1Zhow>/Eaf2<tm1Zhow>,Tg(Pbsn-cre)4Prb/0	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * DBA/2	N	31229879
MGI:6695074	M	MP:0002675	asthenozoospermia	Dnah17<em1Qsh>/Dnah17<em1Qsh>	involves: C57BL/6 * DBA/2J	N	31658987
MGI:6695074	M	MP:0002687	oligozoospermia	Dnah17<em1Qsh>/Dnah17<em1Qsh>	involves: C57BL/6 * DBA/2J	N	31658987
MGI:6695074	M	MP:0009838	abnormal sperm axoneme morphology	Dnah17<em1Qsh>/Dnah17<em1Qsh>	involves: C57BL/6 * DBA/2J	N	31658987
MGI:6695074	M	MP:0002686	globozoospermia	Dnah17<em1Qsh>/Dnah17<em1Qsh>	involves: C57BL/6 * DBA/2J	N	31658987
MGI:6695075	M	MP:0001935	decreased litter size	Dnah17<em2Qsh>/Dnah17<em2Qsh>	involves: C57BL/6 * DBA/2J	N	31658987
MGI:6695075	M	MP:0009838	abnormal sperm axoneme morphology	Dnah17<em2Qsh>/Dnah17<em2Qsh>	involves: C57BL/6 * DBA/2J	N	31658987
MGI:6695075	M	MP:0001922	reduced male fertility	Dnah17<em2Qsh>/Dnah17<em2Qsh>	involves: C57BL/6 * DBA/2J	N	31658987
MGI:6695125	M	MP:0001147	small testis	Nutm1<tm1Ger>/Nutm1<tm1Ger>	involves: 129S2/SvPasCrl * C57BL/6	N	30257209
MGI:6695125	M	MP:0001155	arrest of spermatogenesis	Nutm1<tm1Ger>/Nutm1<tm1Ger>	involves: 129S2/SvPasCrl * C57BL/6	N	30257209
MGI:6695125	M	MP:0005159	azoospermia	Nutm1<tm1Ger>/Nutm1<tm1Ger>	involves: 129S2/SvPasCrl * C57BL/6	N	30257209
MGI:6695125	M	MP:0001925	male infertility	Nutm1<tm1Ger>/Nutm1<tm1Ger>	involves: 129S2/SvPasCrl * C57BL/6	N	30257209
MGI:6695717	M	MP:0002463	abnormal neutrophil physiology	Fam3d<em1Wko>/Fam3d<em1Wko>	C57BL/6-Fam3d<em1Wko>	N	29853563
MGI:6695717	M	MP:0000222	decreased neutrophil cell number	Fam3d<em1Wko>/Fam3d<em1Wko>	C57BL/6-Fam3d<em1Wko>	N	29853563
MGI:6695717	M	MP:0013023	decreased Ly6C high monocyte number	Fam3d<em1Wko>/Fam3d<em1Wko>	C57BL/6-Fam3d<em1Wko>	N	29853563
MGI:6695717	M	MP:0003884	decreased macrophage cell number	Fam3d<em1Wko>/Fam3d<em1Wko>	C57BL/6-Fam3d<em1Wko>	N	29853563
MGI:6695717	M	MP:0005166	decreased susceptibility to injury	Fam3d<em1Wko>/Fam3d<em1Wko>	C57BL/6-Fam3d<em1Wko>	N	29853563
MGI:6695717	M	MP:0000219	increased neutrophil cell number	Fam3d<em1Wko>/Fam3d<em1Wko>	C57BL/6-Fam3d<em1Wko>	N	29853563
MGI:6695866	F	MP:0004499	increased incidence of tumors by chemical induction	Stk26<tm1.1Zzh>/Stk26<tm1.1Zzh>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129 * 129P2/OlaHsd * C57BL/6 * SJL	N	32271880
MGI:6695867	F	MP:0004499	increased incidence of tumors by chemical induction	Stk26<tm1.1Zzh>/Stk26<+>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129 * 129P2/OlaHsd * C57BL/6 * SJL	N	32271880
MGI:6695934	M	MP:0009355	increased liver triglyceride level	Wdfy2<tm1.1Wgz>/Wdfy2<tm1.1Wgz>	involves: C57BL/6J	N	32641353
MGI:6695934	M	MP:0002079	increased circulating insulin level	Wdfy2<tm1.1Wgz>/Wdfy2<tm1.1Wgz>	involves: C57BL/6J	N	32641353
MGI:6695934	M	MP:0002628	hepatic steatosis	Wdfy2<tm1.1Wgz>/Wdfy2<tm1.1Wgz>	involves: C57BL/6J	N	32641353
MGI:6695934	M	MP:0005331	insulin resistance	Wdfy2<tm1.1Wgz>/Wdfy2<tm1.1Wgz>	involves: C57BL/6J	N	32641353
MGI:6695934	M	MP:0010398	decreased liver glycogen level	Wdfy2<tm1.1Wgz>/Wdfy2<tm1.1Wgz>	involves: C57BL/6J	N	32641353
MGI:6695934	M	MP:0005178	increased circulating cholesterol level	Wdfy2<tm1.1Wgz>/Wdfy2<tm1.1Wgz>	involves: C57BL/6J	N	32641353
MGI:6695934	M	MP:0002981	increased liver weight	Wdfy2<tm1.1Wgz>/Wdfy2<tm1.1Wgz>	involves: C57BL/6J	N	32641353
MGI:6695934	M	MP:0005293	impaired glucose tolerance	Wdfy2<tm1.1Wgz>/Wdfy2<tm1.1Wgz>	involves: C57BL/6J	N	32641353
MGI:6695934	M	MP:0020102	increased hepatic glucose production	Wdfy2<tm1.1Wgz>/Wdfy2<tm1.1Wgz>	involves: C57BL/6J	N	32641353
MGI:6695934	M	MP:0001552	increased circulating triglyceride level	Wdfy2<tm1.1Wgz>/Wdfy2<tm1.1Wgz>	involves: C57BL/6J	N	32641353
MGI:6695934	M	MP:0010027	increased liver cholesterol level	Wdfy2<tm1.1Wgz>/Wdfy2<tm1.1Wgz>	involves: C57BL/6J	N	32641353
MGI:6695981	F	MP:0001262	decreased body weight	Rab39b<em1Jfch>/Rab39b<em1Jfch>	C57BL/6N-Rab39b<em1Jfch>	N	32115408
MGI:6695981	F	MP:0005389	reproductive system phenotype	Rab39b<em1Jfch>/Rab39b<em1Jfch>	C57BL/6N-Rab39b<em1Jfch>	Y	32115408
MGI:6695981	F	MP:0010768	mortality/aging	Rab39b<em1Jfch>/Rab39b<em1Jfch>	C57BL/6N-Rab39b<em1Jfch>	Y	32115408
MGI:6695981	F	MP:0005238	increased brain size	Rab39b<em1Jfch>/Rab39b<em1Jfch>	C57BL/6N-Rab39b<em1Jfch>	N	32115408
MGI:6695981	F	MP:0002176	increased brain weight	Rab39b<em1Jfch>/Rab39b<em1Jfch>	C57BL/6N-Rab39b<em1Jfch>	N	32115408
MGI:6695981	F	MP:0005378	growth/size/body region phenotype	Rab39b<em1Jfch>/Rab39b<em1Jfch>	C57BL/6N-Rab39b<em1Jfch>	Y	32115408
MGI:6695982	M	MP:0005238	increased brain size	Rab39b<em1Jfch>/Y	C57BL/6N-Rab39b<em1Jfch>	N	32115408
MGI:6695982	M	MP:0020395	abnormal response to social novelty	Rab39b<em1Jfch>/Y	C57BL/6N-Rab39b<em1Jfch>	N	32115408
MGI:6695982	M	MP:0000788	abnormal cerebral cortex morphology	Rab39b<em1Jfch>/Y	C57BL/6N-Rab39b<em1Jfch>	N	32115408
MGI:6695982	M	MP:0005389	reproductive system phenotype	Rab39b<em1Jfch>/Y	C57BL/6N-Rab39b<em1Jfch>	Y	32115408
MGI:6695982	M	MP:0002804	abnormal motor learning	Rab39b<em1Jfch>/Y	C57BL/6N-Rab39b<em1Jfch>	N	32115408
MGI:6695982	M	MP:0010768	mortality/aging	Rab39b<em1Jfch>/Y	C57BL/6N-Rab39b<em1Jfch>	Y	32115408
MGI:6695982	M	MP:0005386	behavior/neurological phenotype	Rab39b<em1Jfch>/Y	C57BL/6N-Rab39b<em1Jfch>	Y	32115408
MGI:6695982	M	MP:0005378	growth/size/body region phenotype	Rab39b<em1Jfch>/Y	C57BL/6N-Rab39b<em1Jfch>	Y	32115408
MGI:6695982	M	MP:0001262	decreased body weight	Rab39b<em1Jfch>/Y	C57BL/6N-Rab39b<em1Jfch>	N	32115408
MGI:6695982	M	MP:0002176	increased brain weight	Rab39b<em1Jfch>/Y	C57BL/6N-Rab39b<em1Jfch>	N	32115408
MGI:6695982	M	MP:0020593	increased cerebral cortex cell number	Rab39b<em1Jfch>/Y	C57BL/6N-Rab39b<em1Jfch>	N	32115408
MGI:6695983	M	MP:0002675	asthenozoospermia	Ggnbp1<em1Lchao>/Ggnbp1<em1Lchao>	Not Specified	N	32139124
MGI:6695983	M	MP:0001932	abnormal spermiogenesis	Ggnbp1<em1Lchao>/Ggnbp1<em1Lchao>	Not Specified	N	32139124
MGI:6695983	M	MP:0005578	teratozoospermia	Ggnbp1<em1Lchao>/Ggnbp1<em1Lchao>	Not Specified	N	32139124
MGI:6695983	M	MP:0008898	abnormal acrosome morphology	Ggnbp1<em1Lchao>/Ggnbp1<em1Lchao>	Not Specified	N	32139124
MGI:6695983	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Ggnbp1<em1Lchao>/Ggnbp1<em1Lchao>	Not Specified	N	32139124
MGI:6695983	M	MP:0009237	kinked sperm flagellum	Ggnbp1<em1Lchao>/Ggnbp1<em1Lchao>	Not Specified	N	32139124
MGI:6695983	M	MP:0009230	abnormal sperm head morphology	Ggnbp1<em1Lchao>/Ggnbp1<em1Lchao>	Not Specified	N	32139124
MGI:6695983	M	MP:0001925	male infertility	Ggnbp1<em1Lchao>/Ggnbp1<em1Lchao>	Not Specified	N	32139124
MGI:6695983	M	MP:0005165	increased susceptibility to injury	Ggnbp1<em1Lchao>/Ggnbp1<em1Lchao>	Not Specified	N	32139124
MGI:6696047	M	MP:0005389	reproductive system phenotype	Cimip4<em1Mngx>/Cimip4<em1Mngx>	C57BL/6-Cimip4<em1Mngx>	Y	32821546
MGI:6696071	F	MP:0014443	impaired polar body extrusion	Zar1l<em1Hyfn>/Zar1l<em1Hyfn>	involves: C57BL/6 * ICR	N	31598710
MGI:6696071	F	MP:0005168	abnormal female meiosis	Zar1l<em1Hyfn>/Zar1l<em1Hyfn>	involves: C57BL/6 * ICR	N	31598710
MGI:6696071	F	MP:0005389	reproductive system phenotype	Zar1l<em1Hyfn>/Zar1l<em1Hyfn>	involves: C57BL/6 * ICR	Y	31598710
MGI:6696072	F	MP:0005168	abnormal female meiosis	Zar1<em1Hyfn>/Zar1<em1Hyfn>	involves: C57BL/6 * ICR	N	31598710
MGI:6696072	F	MP:0001926	female infertility	Zar1<em1Hyfn>/Zar1<em1Hyfn>	involves: C57BL/6 * ICR	N	31598710
MGI:6696072	F	MP:0003718	maternal effect	Zar1<em1Hyfn>/Zar1<em1Hyfn>	involves: C57BL/6 * ICR	N	31598710
MGI:6696072	F	MP:0014443	impaired polar body extrusion	Zar1<em1Hyfn>/Zar1<em1Hyfn>	involves: C57BL/6 * ICR	N	31598710
MGI:6696073	F	MP:0014443	impaired polar body extrusion	Zar1<em1Hyfn>/Zar1<em1Hyfn>,Zar1l<em1Hyfn>/Zar1l<em1Hyfn>	involves: C57BL/6 * ICR	N	31598710
MGI:6696073	F	MP:0003718	maternal effect	Zar1<em1Hyfn>/Zar1<em1Hyfn>,Zar1l<em1Hyfn>/Zar1l<em1Hyfn>	involves: C57BL/6 * ICR	N	31598710
MGI:6696073	F	MP:0005168	abnormal female meiosis	Zar1<em1Hyfn>/Zar1<em1Hyfn>,Zar1l<em1Hyfn>/Zar1l<em1Hyfn>	involves: C57BL/6 * ICR	N	31598710
MGI:6696073	F	MP:0004024	aneuploidy	Zar1<em1Hyfn>/Zar1<em1Hyfn>,Zar1l<em1Hyfn>/Zar1l<em1Hyfn>	involves: C57BL/6 * ICR	N	31598710
MGI:6696073	F	MP:0010767	abnormal female meiosis I arrest	Zar1<em1Hyfn>/Zar1<em1Hyfn>,Zar1l<em1Hyfn>/Zar1l<em1Hyfn>	involves: C57BL/6 * ICR	N	31598710
MGI:6696142	M	MP:0000242	impaired fertilization	Igh<tm3(IGH)Vlcg>/Igh<tm3(IGH)Vlcg>	involves: 129S6/SvEvTac * C57BL/6NTac	N	30289441
MGI:6696142	M	MP:0031012	impaired sperm migration in female genital tract	Igh<tm3(IGH)Vlcg>/Igh<tm3(IGH)Vlcg>	involves: 129S6/SvEvTac * C57BL/6NTac	N	30289441
MGI:6696142	M	MP:0001922	reduced male fertility	Igh<tm3(IGH)Vlcg>/Igh<tm3(IGH)Vlcg>	involves: 129S6/SvEvTac * C57BL/6NTac	N	30289441
MGI:6696142	M	MP:0001935	decreased litter size	Igh<tm3(IGH)Vlcg>/Igh<tm3(IGH)Vlcg>	involves: 129S6/SvEvTac * C57BL/6NTac	N	30289441
MGI:6696292	M	MP:0000220	increased monocyte cell number	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0000691	enlarged spleen	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0000221	decreased leukocyte cell number	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0013705	decreased megakaryocyte-erythroid progenitor cell number	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0002396	abnormal hematopoietic system morphology/development	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0000322	increased granulocyte number	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0010763	abnormal hematopoietic stem cell physiology	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0008973	decreased erythroid progenitor cell number	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0010067	increased red blood cell distribution width	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0004809	increased hematopoietic stem cell number	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0000240	extramedullary hematopoiesis	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0005017	decreased B cell number	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0013707	abnormal hematopoietic precursor cell morphology	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0013891	increased common myeloid progenitor cell number	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0013893	decreased common lymphocyte progenitor cell number	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696292	M	MP:0013696	increased granulocyte monocyte progenitor cell number	Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696300	M	MP:0013658	abnormal myeloid cell morphology	Runx1<tm1Soga>/Runx1<tm1Soga>,Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696300	M	MP:0004809	increased hematopoietic stem cell number	Runx1<tm1Soga>/Runx1<tm1Soga>,Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696300	M	MP:0002590	increased mean corpuscular volume	Runx1<tm1Soga>/Runx1<tm1Soga>,Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696300	M	MP:0008973	decreased erythroid progenitor cell number	Runx1<tm1Soga>/Runx1<tm1Soga>,Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696300	M	MP:0001577	anemia	Runx1<tm1Soga>/Runx1<tm1Soga>,Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696300	M	MP:0009278	abnormal bone marrow cell physiology	Runx1<tm1Soga>/Runx1<tm1Soga>,Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696300	M	MP:0000221	decreased leukocyte cell number	Runx1<tm1Soga>/Runx1<tm1Soga>,Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696300	M	MP:0010067	increased red blood cell distribution width	Runx1<tm1Soga>/Runx1<tm1Soga>,Stag2<tm1.1Soga>/Y,Tg(Mx1-cre)1Cgn/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	32249213
MGI:6696394	F	MP:0009008	delayed estrous cycle	Polr3h<em2Cfe>/Polr3h<em2Cfe>	involves: C57BL/6J * SJL/J	N	30830215
MGI:6696394	F	MP:0011129	decreased tertiary ovarian follicle number	Polr3h<em2Cfe>/Polr3h<em2Cfe>	involves: C57BL/6J * SJL/J	N	30830215
MGI:6696394	F	MP:0011125	decreased primary ovarian follicle number	Polr3h<em2Cfe>/Polr3h<em2Cfe>	involves: C57BL/6J * SJL/J	N	30830215
MGI:6696394	M	MP:0008940	delayed balanopreputial separation	Polr3h<em2Cfe>/Polr3h<em2Cfe>	involves: C57BL/6J * SJL/J	N	30830215
MGI:6696437	M	MP:0001925	male infertility	Del(3Dcst1-Dcst2)1Nino/Del(3Dcst1-Dcst2)1Nino	involves: 129 * C57BL/6	N	33871360
MGI:6696437	M	MP:0031010	failure of sperm-egg fusion	Del(3Dcst1-Dcst2)1Nino/Del(3Dcst1-Dcst2)1Nino	involves: 129 * C57BL/6	N	33871360
MGI:6696437	M	MP:0000242	impaired fertilization	Del(3Dcst1-Dcst2)1Nino/Del(3Dcst1-Dcst2)1Nino	involves: 129 * C57BL/6	N	33871360
MGI:6696438	M	MP:0000242	impaired fertilization	Del(3Dcst1-Dcst2)1Nino/Del(3Dcst1-Dcst2)1Nino,Tg(Dcst1)1Osb/0	involves: 129 * C57BL/6 * DBA/2J	N	33871360
MGI:6696439	M	MP:0000242	impaired fertilization	Del(3Dcst1-Dcst2)1Nino/Del(3Dcst1-Dcst2)1Nino,Tg(Clgn-Dcst2)1Nino/0	involves: 129 * C57BL/6 * DBA/2J	N	33871360
MGI:6696440	M	MP:0005389	reproductive system phenotype	Del(3Dcst1-Dcst2)1Nino/Del(3Dcst1-Dcst2)1Nino,Tg(Clgn-Dcst2)1Nino/0,Tg(Dcst1)1Osb/0	involves: 129 * C57BL/6 * DBA/2J	Y	33871360
MGI:6696441	M	MP:0001925	male infertility	Dcst1<em1Nino>/Dcst1<em1Nino>	involves: 129 * C57BL/6	N	33871360
MGI:6696441	M	MP:0000242	impaired fertilization	Dcst1<em1Nino>/Dcst1<em1Nino>	involves: 129 * C57BL/6	N	33871360
MGI:6696442	M	MP:0001925	male infertility	Dcst2<em1Nino>/Dcst2<em1Nino>	involves: 129 * C57BL/6	N	33871360
MGI:6696442	M	MP:0000242	impaired fertilization	Dcst2<em1Nino>/Dcst2<em1Nino>	involves: 129 * C57BL/6	N	33871360
MGI:6696443	M	MP:0000242	impaired fertilization	Spaca6<em1Nino>/Spaca6<em1Nino>	involves: 129 * C57BL/6	N	33871360
MGI:6696638	F	MP:0002833	increased heart weight	4921509C19Rik<tm1.1(KOMP)Vlcg>/4921509C19Rik<tm1.1(KOMP)Vlcg>	B6N(Cg)-4921509C19Rik<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6696638	F	MP:0005562	decreased mean corpuscular hemoglobin	4921509C19Rik<tm1.1(KOMP)Vlcg>/4921509C19Rik<tm1.1(KOMP)Vlcg>	B6N(Cg)-4921509C19Rik<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6696638	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	4921509C19Rik<tm1.1(KOMP)Vlcg>/4921509C19Rik<tm1.1(KOMP)Vlcg>	B6N(Cg)-4921509C19Rik<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:6696639	M	MP:0003928	increased heart rate variability	4931406C07Rik<tm1b(EUCOMM)Wtsi>/4931406C07Rik<tm1b(EUCOMM)Wtsi>	C57BL/6N-4931406C07Rik<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6696640	M	MP:0000689	abnormal spleen morphology	A2ml1<em1(IMPC)Tcp>/A2ml1<+>	C57BL/6N-A2ml1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696640	M	MP:0000157	abnormal sternum morphology	A2ml1<em1(IMPC)Tcp>/A2ml1<+>	C57BL/6N-A2ml1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696641	F	MP:0002699	abnormal vitreous body morphology	AA986860<em1(IMPC)Mbp>/AA986860<em1(IMPC)Mbp>	C57BL/6N-AA986860<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696641	F	MP:0002135	abnormal kidney morphology	AA986860<em1(IMPC)Mbp>/AA986860<em1(IMPC)Mbp>	C57BL/6N-AA986860<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696641	F	MP:0002989	small kidney	AA986860<em1(IMPC)Mbp>/AA986860<em1(IMPC)Mbp>	C57BL/6N-AA986860<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696642	F	MP:0001399	hyperactivity	Aatf<em1(IMPC)J>/Aatf<+>	C57BL/6NJ-Aatf<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696643	M	MP:0000689	abnormal spleen morphology	Acad10<em1(IMPC)Tcp>/Acad10<em1(IMPC)Tcp>	C57BL/6N-Acad10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696646	F	MP:0001399	hyperactivity	Actl6b<em1(IMPC)J>/Actl6b<+>	C57BL/6NJ-Actl6b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696648	M	MP:0001304	cataract	Adamts6<em1(IMPC)Mbp>/Adamts6<+>	C57BL/6N-Adamts6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696648	F	MP:0002989	small kidney	Adamts6<em1(IMPC)Mbp>/Adamts6<+>	C57BL/6N-Adamts6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696648	M	MP:0002699	abnormal vitreous body morphology	Adamts6<em1(IMPC)Mbp>/Adamts6<+>	C57BL/6N-Adamts6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696648	F	MP:0002092	abnormal eye morphology	Adamts6<em1(IMPC)Mbp>/Adamts6<+>	C57BL/6N-Adamts6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696648	F	MP:0002135	abnormal kidney morphology	Adamts6<em1(IMPC)Mbp>/Adamts6<+>	C57BL/6N-Adamts6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696649	M	MP:0000219	increased neutrophil cell number	Adgrl4<em1(IMPC)Mbp>/Adgrl4<em1(IMPC)Mbp>	C57BL/6N-Adgrl4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696649	F	MP:0000598	abnormal liver morphology	Adgrl4<em1(IMPC)Mbp>/Adgrl4<em1(IMPC)Mbp>	C57BL/6N-Adgrl4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696649	M	MP:0002574	increased vertical activity	Adgrl4<em1(IMPC)Mbp>/Adgrl4<em1(IMPC)Mbp>	C57BL/6N-Adgrl4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696649	F	MP:0002060	abnormal skin morphology	Adgrl4<em1(IMPC)Mbp>/Adgrl4<em1(IMPC)Mbp>	C57BL/6N-Adgrl4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696649	F	MP:0000601	small liver	Adgrl4<em1(IMPC)Mbp>/Adgrl4<em1(IMPC)Mbp>	C57BL/6N-Adgrl4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696649	F	MP:0002092	abnormal eye morphology	Adgrl4<em1(IMPC)Mbp>/Adgrl4<em1(IMPC)Mbp>	C57BL/6N-Adgrl4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696650	M	MP:0000274	enlarged heart	Adrb2<em1(IMPC)Mbp>/Adrb2<em1(IMPC)Mbp>	C57BL/6N-Adrb2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696650	F	MP:0000598	abnormal liver morphology	Adrb2<em1(IMPC)Mbp>/Adrb2<em1(IMPC)Mbp>	C57BL/6N-Adrb2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696650	F	MP:0002060	abnormal skin morphology	Adrb2<em1(IMPC)Mbp>/Adrb2<em1(IMPC)Mbp>	C57BL/6N-Adrb2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696650	F	MP:0000691	enlarged spleen	Adrb2<em1(IMPC)Mbp>/Adrb2<em1(IMPC)Mbp>	C57BL/6N-Adrb2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696650	F	MP:0000689	abnormal spleen morphology	Adrb2<em1(IMPC)Mbp>/Adrb2<em1(IMPC)Mbp>	C57BL/6N-Adrb2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696650	F	MP:0002092	abnormal eye morphology	Adrb2<em1(IMPC)Mbp>/Adrb2<em1(IMPC)Mbp>	C57BL/6N-Adrb2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696650	F	MP:0000601	small liver	Adrb2<em1(IMPC)Mbp>/Adrb2<em1(IMPC)Mbp>	C57BL/6N-Adrb2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696650	M	MP:0000266	abnormal heart morphology	Adrb2<em1(IMPC)Mbp>/Adrb2<em1(IMPC)Mbp>	C57BL/6N-Adrb2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696651	F	MP:0002135	abnormal kidney morphology	a<em1(IMPC)Mbp>/a<em1(IMPC)Mbp>	C57BL/6N-a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696651	F	MP:0002989	small kidney	a<em1(IMPC)Mbp>/a<em1(IMPC)Mbp>	C57BL/6N-a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696651	M	MP:0002699	abnormal vitreous body morphology	a<em1(IMPC)Mbp>/a<em1(IMPC)Mbp>	C57BL/6N-a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696651	M	MP:0001304	cataract	a<em1(IMPC)Mbp>/a<em1(IMPC)Mbp>	C57BL/6N-a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696653	F	MP:0002699	abnormal vitreous body morphology	Ahctf1<em1(IMPC)Hmgu>/Ahctf1<+>	C57BL/6N-Ahctf1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696654	F	MP:0002060	abnormal skin morphology	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696654	M	MP:0001304	cataract	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696654	F	MP:0000702	enlarged lymph nodes	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696654	F	MP:0000598	abnormal liver morphology	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696654	F	MP:0009342	enlarged gallbladder	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696654	F	MP:0002339	abnormal lymph node morphology	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696654	M	MP:0002699	abnormal vitreous body morphology	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696654	F	MP:0005292	improved glucose tolerance	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696654	F	MP:0005084	abnormal gallbladder morphology	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696654	F	MP:0000601	small liver	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696654	F	MP:0000689	abnormal spleen morphology	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696654	F	MP:0000691	enlarged spleen	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696654	F	MP:0002092	abnormal eye morphology	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696654	F	MP:0001297	microphthalmia	Akap13<em1(IMPC)Mbp>/Akap13<em1(IMPC)Mbp>	C57BL/6N-Akap13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696659	M	MP:0000689	abnormal spleen morphology	Arhgef2<em1(IMPC)Mbp>/Arhgef2<em1(IMPC)Mbp>	C57BL/6N-Arhgef2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696659	F	MP:0002060	abnormal skin morphology	Arhgef2<em1(IMPC)Mbp>/Arhgef2<em1(IMPC)Mbp>	C57BL/6N-Arhgef2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696659	M	MP:0005568	increased circulating total protein level	Arhgef2<em1(IMPC)Mbp>/Arhgef2<em1(IMPC)Mbp>	C57BL/6N-Arhgef2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696659	M	MP:0000692	small spleen	Arhgef2<em1(IMPC)Mbp>/Arhgef2<em1(IMPC)Mbp>	C57BL/6N-Arhgef2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696659	M	MP:0003179	thrombocytopenia	Arhgef2<em1(IMPC)Mbp>/Arhgef2<em1(IMPC)Mbp>	C57BL/6N-Arhgef2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696659	M	MP:0002152	abnormal brain morphology	Arhgef2<em1(IMPC)Mbp>/Arhgef2<em1(IMPC)Mbp>	C57BL/6N-Arhgef2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696659	M	MP:0000774	decreased brain size	Arhgef2<em1(IMPC)Mbp>/Arhgef2<em1(IMPC)Mbp>	C57BL/6N-Arhgef2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696659	F	MP:0002968	increased circulating alkaline phosphatase level	Arhgef2<em1(IMPC)Mbp>/Arhgef2<em1(IMPC)Mbp>	C57BL/6N-Arhgef2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696659	M	MP:0002965	increased circulating serum albumin level	Arhgef2<em1(IMPC)Mbp>/Arhgef2<em1(IMPC)Mbp>	C57BL/6N-Arhgef2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696659	F	MP:0000598	abnormal liver morphology	Arhgef2<em1(IMPC)Mbp>/Arhgef2<em1(IMPC)Mbp>	C57BL/6N-Arhgef2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696659	F	MP:0000601	small liver	Arhgef2<em1(IMPC)Mbp>/Arhgef2<em1(IMPC)Mbp>	C57BL/6N-Arhgef2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696661	F	MP:0001417	decreased exploration in new environment	Armcx1<em1(IMPC)Mbp>/Armcx1<em1(IMPC)Mbp>	C57BL/6N-Armcx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696662	M	MP:0010124	decreased bone mineral content	Arpc1a<em1(IMPC)J>/Arpc1a<+>	C57BL/6NJ-Arpc1a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696665	F	MP:0003961	decreased lean body mass	Bbs2<em2(IMPC)Wtsi>/Bbs2<+>	C57BL/6N-Bbs2<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696665	M	MP:0010123	increased bone mineral content	Bbs2<em2(IMPC)Wtsi>/Bbs2<+>	C57BL/6N-Bbs2<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696666	M	MP:0010124	decreased bone mineral content	Bcap29<em1(IMPC)J>/Bcap29<em1(IMPC)J>	C57BL/6NJ-Bcap29<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696666	M	MP:0000063	decreased bone mineral density	Bcap29<em1(IMPC)J>/Bcap29<em1(IMPC)J>	C57BL/6NJ-Bcap29<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696666	M	MP:0010097	abnormal retina blood vessel morphology	Bcap29<em1(IMPC)J>/Bcap29<em1(IMPC)J>	C57BL/6NJ-Bcap29<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696667	M	MP:0002606	increased basophil cell number	Bcar3<em1(IMPC)Mbp>/Bcar3<em1(IMPC)Mbp>	C57BL/6N-Bcar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696667	M	MP:0002079	increased circulating insulin level	Bcar3<em1(IMPC)Mbp>/Bcar3<em1(IMPC)Mbp>	C57BL/6N-Bcar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696667	F	MP:0002989	small kidney	Bcar3<em1(IMPC)Mbp>/Bcar3<em1(IMPC)Mbp>	C57BL/6N-Bcar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696667	F	MP:0002092	abnormal eye morphology	Bcar3<em1(IMPC)Mbp>/Bcar3<em1(IMPC)Mbp>	C57BL/6N-Bcar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696667	M	MP:0000194	increased circulating calcium level	Bcar3<em1(IMPC)Mbp>/Bcar3<em1(IMPC)Mbp>	C57BL/6N-Bcar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696667	F	MP:0002135	abnormal kidney morphology	Bcar3<em1(IMPC)Mbp>/Bcar3<em1(IMPC)Mbp>	C57BL/6N-Bcar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696668	F	MP:0005553	increased circulating creatinine level	Bcl7c<em1(IMPC)J>/Bcl7c<em1(IMPC)J>	C57BL/6NJ-Bcl7c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696668	M	MP:0000195	decreased circulating calcium level	Bcl7c<em1(IMPC)J>/Bcl7c<em1(IMPC)J>	C57BL/6NJ-Bcl7c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696670	F	MP:0002989	small kidney	Bst2<em1(IMPC)Mbp>/Bst2<em1(IMPC)Mbp>	C57BL/6N-Bst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696670	F	MP:0002135	abnormal kidney morphology	Bst2<em1(IMPC)Mbp>/Bst2<em1(IMPC)Mbp>	C57BL/6N-Bst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696670	F	MP:0002060	abnormal skin morphology	Bst2<em1(IMPC)Mbp>/Bst2<em1(IMPC)Mbp>	C57BL/6N-Bst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696670	F	MP:0000601	small liver	Bst2<em1(IMPC)Mbp>/Bst2<em1(IMPC)Mbp>	C57BL/6N-Bst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696670	F	MP:0000598	abnormal liver morphology	Bst2<em1(IMPC)Mbp>/Bst2<em1(IMPC)Mbp>	C57BL/6N-Bst2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696671	M	MP:0001925	male infertility	Catsper3<em2(IMPC)Mbp>/Catsper3<em2(IMPC)Mbp>	C57BL/6N-Catsper3<em2(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696671	F	MP:0000639	abnormal adrenal gland morphology	Catsper3<em2(IMPC)Mbp>/Catsper3<em2(IMPC)Mbp>	C57BL/6N-Catsper3<em2(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696671	M	MP:0002092	abnormal eye morphology	Catsper3<em2(IMPC)Mbp>/Catsper3<em2(IMPC)Mbp>	C57BL/6N-Catsper3<em2(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696671	F	MP:0000642	enlarged adrenal glands	Catsper3<em2(IMPC)Mbp>/Catsper3<em2(IMPC)Mbp>	C57BL/6N-Catsper3<em2(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696673	M	MP:0000745	tremors	Ccdc125<em1(IMPC)Hmgu>/Ccdc125<em1(IMPC)Hmgu>	C57BL/6N-Ccdc125<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696673	M	MP:0011965	decreased total retina thickness	Ccdc125<em1(IMPC)Hmgu>/Ccdc125<em1(IMPC)Hmgu>	C57BL/6N-Ccdc125<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696675	M	MP:0002574	increased vertical activity	Cchcr1<em1(IMPC)J>/Cchcr1<em1(IMPC)J>	C57BL/6NJ-Cchcr1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696675	M	MP:0001399	hyperactivity	Cchcr1<em1(IMPC)J>/Cchcr1<em1(IMPC)J>	C57BL/6NJ-Cchcr1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696676	F	MP:0000689	abnormal spleen morphology	Ccno<em1(IMPC)Mbp>/Ccno<+>	C57BL/6N-Ccno<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696676	F	MP:0000691	enlarged spleen	Ccno<em1(IMPC)Mbp>/Ccno<+>	C57BL/6N-Ccno<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696677	M	MP:0001488	increased startle reflex	Cct3<em1(IMPC)Tcp>/Cct3<+>	C57BL/6N-Cct3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696677	F	MP:0005562	decreased mean corpuscular hemoglobin	Cct3<em1(IMPC)Tcp>/Cct3<+>	C57BL/6N-Cct3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696679	F	MP:0011959	abnormal eye posterior chamber depth	Cd320<em1(IMPC)Bay>/Cd320<em1(IMPC)Bay>	C57BL/6N-Cd320<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6696680	M	MP:0002644	decreased circulating triglyceride level	Cd36<em1(IMPC)Mbp>/Cd36<em1(IMPC)Mbp>	C57BL/6N-Cd36<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696680	F	MP:0002060	abnormal skin morphology	Cd36<em1(IMPC)Mbp>/Cd36<em1(IMPC)Mbp>	C57BL/6N-Cd36<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696680	M	MP:0000774	decreased brain size	Cd36<em1(IMPC)Mbp>/Cd36<em1(IMPC)Mbp>	C57BL/6N-Cd36<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696680	F	MP:0003795	abnormal bone structure	Cd36<em1(IMPC)Mbp>/Cd36<em1(IMPC)Mbp>	C57BL/6N-Cd36<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696680	M	MP:0002152	abnormal brain morphology	Cd36<em1(IMPC)Mbp>/Cd36<em1(IMPC)Mbp>	C57BL/6N-Cd36<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696680	F	MP:0002833	increased heart weight	Cd36<em1(IMPC)Mbp>/Cd36<em1(IMPC)Mbp>	C57BL/6N-Cd36<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696680	M	MP:0000598	abnormal liver morphology	Cd36<em1(IMPC)Mbp>/Cd36<em1(IMPC)Mbp>	C57BL/6N-Cd36<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696680	M	MP:0000599	enlarged liver	Cd36<em1(IMPC)Mbp>/Cd36<em1(IMPC)Mbp>	C57BL/6N-Cd36<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696681	M	MP:0001399	hyperactivity	Cdc37<em1(IMPC)J>/Cdc37<+>	C57BL/6NJ-Cdc37<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696681	F	MP:0002968	increased circulating alkaline phosphatase level	Cdc37<em1(IMPC)J>/Cdc37<+>	C57BL/6NJ-Cdc37<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696681	M	MP:0001488	increased startle reflex	Cdc37<em1(IMPC)J>/Cdc37<+>	C57BL/6NJ-Cdc37<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696686	M	MP:0002060	abnormal skin morphology	Chd6<em1(IMPC)Mbp>/Chd6<em1(IMPC)Mbp>	C57BL/6N-Chd6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696687	F	MP:0001325	abnormal retina morphology	Chordc1<em1(IMPC)Mbp>/Chordc1<+>	C57BL/6N-Chordc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696687	M	MP:0000219	increased neutrophil cell number	Chordc1<em1(IMPC)Mbp>/Chordc1<+>	C57BL/6N-Chordc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696687	M	MP:0005016	decreased lymphocyte cell number	Chordc1<em1(IMPC)Mbp>/Chordc1<+>	C57BL/6N-Chordc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696687	M	MP:0001304	cataract	Chordc1<em1(IMPC)Mbp>/Chordc1<+>	C57BL/6N-Chordc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696687	F	MP:0002060	abnormal skin morphology	Chordc1<em1(IMPC)Mbp>/Chordc1<+>	C57BL/6N-Chordc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696688	F	MP:0000709	enlarged thymus	Churc1<tm1b(EUCOMM)Wtsi>/Churc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Churc1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696688	F	MP:0002092	abnormal eye morphology	Churc1<tm1b(EUCOMM)Wtsi>/Churc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Churc1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696688	F	MP:0000689	abnormal spleen morphology	Churc1<tm1b(EUCOMM)Wtsi>/Churc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Churc1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696688	M	MP:0000266	abnormal heart morphology	Churc1<tm1b(EUCOMM)Wtsi>/Churc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Churc1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696688	M	MP:0000274	enlarged heart	Churc1<tm1b(EUCOMM)Wtsi>/Churc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Churc1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696688	F	MP:0000703	abnormal thymus morphology	Churc1<tm1b(EUCOMM)Wtsi>/Churc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Churc1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696688	F	MP:0013772	increased effector memory T-helper cell number	Churc1<tm1b(EUCOMM)Wtsi>/Churc1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Churc1<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696689	M	MP:0002599	increased mean platelet volume	Cisd1<em1(IMPC)Hmgu>/Cisd1<em1(IMPC)Hmgu>	C57BL/6N-Cisd1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696689	M	MP:0003019	increased circulating chloride level	Cisd1<em1(IMPC)Hmgu>/Cisd1<em1(IMPC)Hmgu>	C57BL/6N-Cisd1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696694	M	MP:0000691	enlarged spleen	Cnr2<em1(IMPC)Mbp>/Cnr2<em1(IMPC)Mbp>	C57BL/6N-Cnr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696694	F	MP:0002060	abnormal skin morphology	Cnr2<em1(IMPC)Mbp>/Cnr2<em1(IMPC)Mbp>	C57BL/6N-Cnr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696694	F	MP:0000494	abnormal cecum morphology	Cnr2<em1(IMPC)Mbp>/Cnr2<em1(IMPC)Mbp>	C57BL/6N-Cnr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696694	F	MP:0002989	small kidney	Cnr2<em1(IMPC)Mbp>/Cnr2<em1(IMPC)Mbp>	C57BL/6N-Cnr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696694	F	MP:0002135	abnormal kidney morphology	Cnr2<em1(IMPC)Mbp>/Cnr2<em1(IMPC)Mbp>	C57BL/6N-Cnr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696694	F	MP:0009476	enlarged cecum	Cnr2<em1(IMPC)Mbp>/Cnr2<em1(IMPC)Mbp>	C57BL/6N-Cnr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696694	M	MP:0000689	abnormal spleen morphology	Cnr2<em1(IMPC)Mbp>/Cnr2<em1(IMPC)Mbp>	C57BL/6N-Cnr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696697	F	MP:0001399	hyperactivity	Crisp2<em1(IMPC)Mbp>/Crisp2<em1(IMPC)Mbp>	C57BL/6NCrl-Crisp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6696697	F	MP:0001120	abnormal uterus morphology	Crisp2<em1(IMPC)Mbp>/Crisp2<em1(IMPC)Mbp>	C57BL/6NCrl-Crisp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6696697	M	MP:0020421	increased freezing behavior	Crisp2<em1(IMPC)Mbp>/Crisp2<em1(IMPC)Mbp>	C57BL/6NCrl-Crisp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6696697	F	MP:0009709	hydrometra	Crisp2<em1(IMPC)Mbp>/Crisp2<em1(IMPC)Mbp>	C57BL/6NCrl-Crisp2<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6696698	F	MP:0010052	increased grip strength	Crtac1<em1(IMPC)H>/Crtac1<em1(IMPC)H>	C57BL/6NTac-Crtac1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6696699	M	MP:0001146	abnormal testis morphology	Crygn<em1(IMPC)Hmgu>/Crygn<em1(IMPC)Hmgu>	C57BL/6N-Crygn<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696702	M	MP:0002874	decreased hemoglobin content	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	F	MP:0009456	impaired cued conditioning behavior	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	F	MP:0009142	decreased prepulse inhibition	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	F	MP:0005179	decreased circulating cholesterol level	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	F	MP:0020420	abnormal freezing behavior	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	M	MP:0002644	decreased circulating triglyceride level	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	F	MP:0002590	increased mean corpuscular volume	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	M	MP:0000208	decreased hematocrit	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	M	MP:0005560	decreased circulating glucose level	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	F	MP:0001486	abnormal startle reflex	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	M	MP:0000550	abnormal forelimb morphology	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	F	MP:0005419	decreased circulating serum albumin level	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	M	MP:0000556	abnormal hindlimb morphology	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	M	MP:0001489	decreased startle reflex	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	F	MP:0000691	enlarged spleen	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	F	MP:0005561	increased mean corpuscular hemoglobin	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	M	MP:0001406	abnormal gait	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696702	M	MP:0001392	abnormal locomotor behavior	Ctsa<tm2b(EUCOMM)Hmgu>/Ctsa<tm2b(EUCOMM)Hmgu>	C57BL/6N-Ctsa<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:6696703	M	MP:0010053	decreased grip strength	Cttnbp2nl<em1(IMPC)J>/Cttnbp2nl<em1(IMPC)J>	C57BL/6NJ-Cttnbp2nl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696703	M	MP:0005562	decreased mean corpuscular hemoglobin	Cttnbp2nl<em1(IMPC)J>/Cttnbp2nl<em1(IMPC)J>	C57BL/6NJ-Cttnbp2nl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696703	M	MP:0005565	increased blood urea nitrogen level	Cttnbp2nl<em1(IMPC)J>/Cttnbp2nl<em1(IMPC)J>	C57BL/6NJ-Cttnbp2nl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696703	M	MP:0001488	increased startle reflex	Cttnbp2nl<em1(IMPC)J>/Cttnbp2nl<em1(IMPC)J>	C57BL/6NJ-Cttnbp2nl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696706	M	MP:0002059	abnormal seminal vesicle morphology	Cyp2b9<em1(IMPC)Hmgu>/Cyp2b9<em1(IMPC)Hmgu>	C57BL/6N-Cyp2b9<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696707	F	MP:0002989	small kidney	Cysltr1<em1(IMPC)Mbp>/Cysltr1<em1(IMPC)Mbp>	C57BL/6N-Cysltr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696707	F	MP:0002135	abnormal kidney morphology	Cysltr1<em1(IMPC)Mbp>/Cysltr1<em1(IMPC)Mbp>	C57BL/6N-Cysltr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696708	F	MP:0000601	small liver	Cysltr2<em1(IMPC)Mbp>/Cysltr2<em1(IMPC)Mbp>	C57BL/6N-Cysltr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696708	F	MP:0002989	small kidney	Cysltr2<em1(IMPC)Mbp>/Cysltr2<em1(IMPC)Mbp>	C57BL/6N-Cysltr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696708	F	MP:0000598	abnormal liver morphology	Cysltr2<em1(IMPC)Mbp>/Cysltr2<em1(IMPC)Mbp>	C57BL/6N-Cysltr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696708	F	MP:0000274	enlarged heart	Cysltr2<em1(IMPC)Mbp>/Cysltr2<em1(IMPC)Mbp>	C57BL/6N-Cysltr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696708	F	MP:0000266	abnormal heart morphology	Cysltr2<em1(IMPC)Mbp>/Cysltr2<em1(IMPC)Mbp>	C57BL/6N-Cysltr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696708	F	MP:0002135	abnormal kidney morphology	Cysltr2<em1(IMPC)Mbp>/Cysltr2<em1(IMPC)Mbp>	C57BL/6N-Cysltr2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696712	M	MP:0000702	enlarged lymph nodes	Ddx46<em1(IMPC)Tcp>/Ddx46<+>	C57BL/6N-Ddx46<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696713	F	MP:0000601	small liver	Rigi<em1(IMPC)Mbp>/Rigi<em1(IMPC)Mbp>	C57BL/6N-Rigi<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696713	M	MP:0005293	impaired glucose tolerance	Rigi<em1(IMPC)Mbp>/Rigi<em1(IMPC)Mbp>	C57BL/6N-Rigi<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696713	F	MP:0000598	abnormal liver morphology	Rigi<em1(IMPC)Mbp>/Rigi<em1(IMPC)Mbp>	C57BL/6N-Rigi<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696714	M	MP:0020421	increased freezing behavior	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	M	MP:0003233	prolonged QT interval	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	M	MP:0010068	decreased red blood cell distribution width	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	M	MP:0010506	prolonged RR interval	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	M	MP:0005292	improved glucose tolerance	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	F	MP:0000218	increased leukocyte cell number	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	F	MP:0003795	abnormal bone structure	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	M	MP:0000689	abnormal spleen morphology	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	F	MP:0010124	decreased bone mineral content	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	M	MP:0010052	increased grip strength	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	M	MP:0002059	abnormal seminal vesicle morphology	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	M	MP:0005333	decreased heart rate	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	M	MP:0002644	decreased circulating triglyceride level	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	M	MP:0000157	abnormal sternum morphology	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	M	MP:0001417	decreased exploration in new environment	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	F	MP:0000063	decreased bone mineral density	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696714	F	MP:0003960	increased lean body mass	Dennd5b<em1(IMPC)Tcp>/Dennd5b<em1(IMPC)Tcp>	C57BL/6N-Dennd5b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696717	M	MP:0001566	increased circulating phosphate level	Diaph2<tm1b(EUCOMM)Hmgu>/Y	C57BL/6N-Diaph2<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6696719	F	MP:0005562	decreased mean corpuscular hemoglobin	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696719	F	MP:0002968	increased circulating alkaline phosphatase level	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696719	F	MP:0002591	decreased mean corpuscular volume	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696719	F	MP:0010124	decreased bone mineral content	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696719	F	MP:0002965	increased circulating serum albumin level	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696719	F	MP:0010053	decreased grip strength	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696719	F	MP:0003795	abnormal bone structure	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696719	F	MP:0003960	increased lean body mass	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696719	F	MP:0005343	increased circulating aspartate transaminase level	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696719	F	MP:0005505	thrombocytosis	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696719	F	MP:0005568	increased circulating total protein level	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696719	F	MP:0002941	increased circulating alanine transaminase level	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696719	F	MP:0010067	increased red blood cell distribution width	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696719	F	MP:0010025	decreased total body fat amount	Dmd<em1(IMPC)Hmgu>/Dmd<em1(IMPC)Hmgu>	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696720	F	MP:0010511	shortened PR interval	Dnaaf1<em1(IMPC)J>/Dnaaf1<+>	C57BL/6NJ-Dnaaf1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696720	M	MP:0000367	abnormal coat/ hair morphology	Dnaaf1<em1(IMPC)J>/Dnaaf1<+>	C57BL/6NJ-Dnaaf1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696721	F	MP:0001566	increased circulating phosphate level	Dnajb14<em1(IMPC)J>/Dnajb14<+>	C57BL/6NJ-Dnajb14<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696721	F	MP:0003795	abnormal bone structure	Dnajb14<em1(IMPC)J>/Dnajb14<+>	C57BL/6NJ-Dnajb14<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696721	F	MP:0010124	decreased bone mineral content	Dnajb14<em1(IMPC)J>/Dnajb14<+>	C57BL/6NJ-Dnajb14<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696722	F	MP:0002637	small uterus	Dop1a<em1(IMPC)Tcp>/Dop1a<em1(IMPC)Tcp>	C57BL/6N-Dop1a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696722	F	MP:0000627	abnormal mammary gland morphology	Dop1a<em1(IMPC)Tcp>/Dop1a<em1(IMPC)Tcp>	C57BL/6N-Dop1a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696723	M	MP:0010053	decreased grip strength	Dpf3<em1(IMPC)J>/Dpf3<em1(IMPC)J>	C57BL/6NJ-Dpf3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696723	M	MP:0001402	decreased locomotor activity	Dpf3<em1(IMPC)J>/Dpf3<em1(IMPC)J>	C57BL/6NJ-Dpf3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696723	M	MP:0000195	decreased circulating calcium level	Dpf3<em1(IMPC)J>/Dpf3<em1(IMPC)J>	C57BL/6NJ-Dpf3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696723	F	MP:0010124	decreased bone mineral content	Dpf3<em1(IMPC)J>/Dpf3<em1(IMPC)J>	C57BL/6NJ-Dpf3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696723	M	MP:0009142	decreased prepulse inhibition	Dpf3<em1(IMPC)J>/Dpf3<em1(IMPC)J>	C57BL/6NJ-Dpf3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696725	F	MP:0001399	hyperactivity	Dusp29<em1(IMPC)J>/Dusp29<em1(IMPC)J>	C57BL/6NJ-Dusp29<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696726	M	MP:0002792	abnormal retina vasculature morphology	Dusp8<em1(IMPC)Mbp>/Dusp8<em1(IMPC)Mbp>	C57BL/6N-Dusp8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696726	M	MP:0005293	impaired glucose tolerance	Dusp8<em1(IMPC)Mbp>/Dusp8<em1(IMPC)Mbp>	C57BL/6N-Dusp8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696726	F	MP:0000691	enlarged spleen	Dusp8<em1(IMPC)Mbp>/Dusp8<em1(IMPC)Mbp>	C57BL/6N-Dusp8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696726	M	MP:0010053	decreased grip strength	Dusp8<em1(IMPC)Mbp>/Dusp8<em1(IMPC)Mbp>	C57BL/6N-Dusp8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696726	M	MP:0002060	abnormal skin morphology	Dusp8<em1(IMPC)Mbp>/Dusp8<em1(IMPC)Mbp>	C57BL/6N-Dusp8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696726	F	MP:0000689	abnormal spleen morphology	Dusp8<em1(IMPC)Mbp>/Dusp8<em1(IMPC)Mbp>	C57BL/6N-Dusp8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696727	M	MP:0005178	increased circulating cholesterol level	Echdc1<em1(IMPC)J>/Echdc1<em1(IMPC)J>	C57BL/6NJ-Echdc1<em1(IMPC)J>/Mmjax	N	38417553
MGI:6696727	M	MP:0001552	increased circulating triglyceride level	Echdc1<em1(IMPC)J>/Echdc1<em1(IMPC)J>	C57BL/6NJ-Echdc1<em1(IMPC)J>/Mmjax	N	38417553
MGI:6696727	M	MP:0003975	increased circulating VLDL triglyceride level	Echdc1<em1(IMPC)J>/Echdc1<em1(IMPC)J>	C57BL/6NJ-Echdc1<em1(IMPC)J>/Mmjax	N	38417553
MGI:6696727	M	MP:0005145	increased circulating VLDL cholesterol level	Echdc1<em1(IMPC)J>/Echdc1<em1(IMPC)J>	C57BL/6NJ-Echdc1<em1(IMPC)J>/Mmjax	N	38417553
MGI:6696727	M	MP:0000182	increased circulating LDL cholesterol level	Echdc1<em1(IMPC)J>/Echdc1<em1(IMPC)J>	C57BL/6NJ-Echdc1<em1(IMPC)J>/Mmjax	N	38417553
MGI:6696728	F	MP:0001126	abnormal ovary morphology	Efcab5<em1(IMPC)Mbp>/Efcab5<em1(IMPC)Mbp>	C57BL/6N-Efcab5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696728	F	MP:0004832	enlarged ovary	Efcab5<em1(IMPC)Mbp>/Efcab5<em1(IMPC)Mbp>	C57BL/6N-Efcab5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696728	M	MP:0001148	enlarged testis	Efcab5<em1(IMPC)Mbp>/Efcab5<em1(IMPC)Mbp>	C57BL/6N-Efcab5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696728	M	MP:0001146	abnormal testis morphology	Efcab5<em1(IMPC)Mbp>/Efcab5<em1(IMPC)Mbp>	C57BL/6N-Efcab5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696729	F	MP:0001399	hyperactivity	Efcc1<em1(IMPC)Tcp>/Efcc1<em1(IMPC)Tcp>	C57BL/6N-Efcc1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696729	F	MP:0002060	abnormal skin morphology	Efcc1<em1(IMPC)Tcp>/Efcc1<em1(IMPC)Tcp>	C57BL/6N-Efcc1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696729	M	MP:0005562	decreased mean corpuscular hemoglobin	Efcc1<em1(IMPC)Tcp>/Efcc1<em1(IMPC)Tcp>	C57BL/6N-Efcc1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696730	F	MP:0000266	abnormal heart morphology	Enkd1<tm1.1(KOMP)Vlcg>/Enkd1<tm1.1(KOMP)Vlcg>	C57BL/6N-Enkd1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6696730	F	MP:0000274	enlarged heart	Enkd1<tm1.1(KOMP)Vlcg>/Enkd1<tm1.1(KOMP)Vlcg>	C57BL/6N-Enkd1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6696731	M	MP:0001364	decreased anxiety-related response	Epha3<em1(IMPC)Mbp>/Epha3<em1(IMPC)Mbp>	C57BL/6N-Epha3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696731	M	MP:0020870	decreased thigmotaxis	Epha3<em1(IMPC)Mbp>/Epha3<em1(IMPC)Mbp>	C57BL/6N-Epha3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696731	F	MP:0003068	enlarged kidney	Epha3<em1(IMPC)Mbp>/Epha3<em1(IMPC)Mbp>	C57BL/6N-Epha3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696731	F	MP:0000691	enlarged spleen	Epha3<em1(IMPC)Mbp>/Epha3<em1(IMPC)Mbp>	C57BL/6N-Epha3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696731	M	MP:0000692	small spleen	Epha3<em1(IMPC)Mbp>/Epha3<em1(IMPC)Mbp>	C57BL/6N-Epha3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696731	F	MP:0003402	decreased liver weight	Epha3<em1(IMPC)Mbp>/Epha3<em1(IMPC)Mbp>	C57BL/6N-Epha3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696731	M	MP:0004924	abnormal behavior	Epha3<em1(IMPC)Mbp>/Epha3<em1(IMPC)Mbp>	C57BL/6N-Epha3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696731	M	MP:0001399	hyperactivity	Epha3<em1(IMPC)Mbp>/Epha3<em1(IMPC)Mbp>	C57BL/6N-Epha3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696731	F	MP:0002135	abnormal kidney morphology	Epha3<em1(IMPC)Mbp>/Epha3<em1(IMPC)Mbp>	C57BL/6N-Epha3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696732	M	MP:0001556	increased circulating HDL cholesterol level	Ercc8<em1(IMPC)H>/Ercc8<em1(IMPC)H>	C57BL/6N-Ercc8<em1(IMPC)H>/H	N	MGI:5576271
MGI:6696732	M	MP:0005178	increased circulating cholesterol level	Ercc8<em1(IMPC)H>/Ercc8<em1(IMPC)H>	C57BL/6N-Ercc8<em1(IMPC)H>/H	N	MGI:5576271
MGI:6696733	M	MP:0000689	abnormal spleen morphology	Evc2<em1(IMPC)Mbp>/Evc2<em1(IMPC)Mbp>	C57BL/6N-Evc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696733	F	MP:0030610	absent teeth	Evc2<em1(IMPC)Mbp>/Evc2<em1(IMPC)Mbp>	C57BL/6N-Evc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696733	M	MP:0000692	small spleen	Evc2<em1(IMPC)Mbp>/Evc2<em1(IMPC)Mbp>	C57BL/6N-Evc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696733	M	MP:0000494	abnormal cecum morphology	Evc2<em1(IMPC)Mbp>/Evc2<em1(IMPC)Mbp>	C57BL/6N-Evc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696733	M	MP:0000274	enlarged heart	Evc2<em1(IMPC)Mbp>/Evc2<em1(IMPC)Mbp>	C57BL/6N-Evc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696733	F	MP:0002060	abnormal skin morphology	Evc2<em1(IMPC)Mbp>/Evc2<em1(IMPC)Mbp>	C57BL/6N-Evc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696733	F	MP:0001120	abnormal uterus morphology	Evc2<em1(IMPC)Mbp>/Evc2<em1(IMPC)Mbp>	C57BL/6N-Evc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696733	F	MP:0009709	hydrometra	Evc2<em1(IMPC)Mbp>/Evc2<em1(IMPC)Mbp>	C57BL/6N-Evc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696733	F	MP:0005567	decreased circulating total protein level	Evc2<em1(IMPC)Mbp>/Evc2<em1(IMPC)Mbp>	C57BL/6N-Evc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696733	F	MP:0005084	abnormal gallbladder morphology	Evc2<em1(IMPC)Mbp>/Evc2<em1(IMPC)Mbp>	C57BL/6N-Evc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696733	M	MP:0000266	abnormal heart morphology	Evc2<em1(IMPC)Mbp>/Evc2<em1(IMPC)Mbp>	C57BL/6N-Evc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696738	M	MP:0010935	increased airway resistance	Fam219a<em1(IMPC)Ccpcz>/Fam219a<em1(IMPC)Ccpcz>	C57BL/6N-Fam219a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696738	F	MP:0002100	abnormal tooth morphology	Fam219a<em1(IMPC)Ccpcz>/Fam219a<em1(IMPC)Ccpcz>	C57BL/6N-Fam219a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696738	F	MP:0000709	enlarged thymus	Fam219a<em1(IMPC)Ccpcz>/Fam219a<em1(IMPC)Ccpcz>	C57BL/6N-Fam219a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696738	F	MP:0000703	abnormal thymus morphology	Fam219a<em1(IMPC)Ccpcz>/Fam219a<em1(IMPC)Ccpcz>	C57BL/6N-Fam219a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696738	F	MP:0000598	abnormal liver morphology	Fam219a<em1(IMPC)Ccpcz>/Fam219a<em1(IMPC)Ccpcz>	C57BL/6N-Fam219a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696738	M	MP:0001262	decreased body weight	Fam219a<em1(IMPC)Ccpcz>/Fam219a<em1(IMPC)Ccpcz>	C57BL/6N-Fam219a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696739	M	MP:0000689	abnormal spleen morphology	Fgf14<em1(IMPC)Ccpcz>/Fgf14<em1(IMPC)Ccpcz>	C57BL/6N-Fgf14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696739	F	MP:0002968	increased circulating alkaline phosphatase level	Fgf14<em1(IMPC)Ccpcz>/Fgf14<em1(IMPC)Ccpcz>	C57BL/6N-Fgf14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696739	M	MP:0001262	decreased body weight	Fgf14<em1(IMPC)Ccpcz>/Fgf14<em1(IMPC)Ccpcz>	C57BL/6N-Fgf14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696739	F	MP:0002135	abnormal kidney morphology	Fgf14<em1(IMPC)Ccpcz>/Fgf14<em1(IMPC)Ccpcz>	C57BL/6N-Fgf14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696739	F	MP:0002060	abnormal skin morphology	Fgf14<em1(IMPC)Ccpcz>/Fgf14<em1(IMPC)Ccpcz>	C57BL/6N-Fgf14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696739	F	MP:0004174	abnormal spine curvature	Fgf14<em1(IMPC)Ccpcz>/Fgf14<em1(IMPC)Ccpcz>	C57BL/6N-Fgf14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696739	M	MP:0000681	abnormal thyroid gland morphology	Fgf14<em1(IMPC)Ccpcz>/Fgf14<em1(IMPC)Ccpcz>	C57BL/6N-Fgf14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696739	M	MP:0005355	enlarged thyroid gland	Fgf14<em1(IMPC)Ccpcz>/Fgf14<em1(IMPC)Ccpcz>	C57BL/6N-Fgf14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696741	F	MP:0000218	increased leukocyte cell number	Fndc3a<em1(IMPC)Tcp>/Fndc3a<em1(IMPC)Tcp>	C57BL/6N-Fndc3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696741	F	MP:0002834	decreased heart weight	Fndc3a<em1(IMPC)Tcp>/Fndc3a<em1(IMPC)Tcp>	C57BL/6N-Fndc3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696741	M	MP:0005419	decreased circulating serum albumin level	Fndc3a<em1(IMPC)Tcp>/Fndc3a<em1(IMPC)Tcp>	C57BL/6N-Fndc3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696741	F	MP:0002792	abnormal retina vasculature morphology	Fndc3a<em1(IMPC)Tcp>/Fndc3a<em1(IMPC)Tcp>	C57BL/6N-Fndc3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696741	F	MP:0002764	short tibia	Fndc3a<em1(IMPC)Tcp>/Fndc3a<em1(IMPC)Tcp>	C57BL/6N-Fndc3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696741	F	MP:0005013	increased lymphocyte cell number	Fndc3a<em1(IMPC)Tcp>/Fndc3a<em1(IMPC)Tcp>	C57BL/6N-Fndc3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696741	F	MP:0003795	abnormal bone structure	Fndc3a<em1(IMPC)Tcp>/Fndc3a<em1(IMPC)Tcp>	C57BL/6N-Fndc3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696741	F	MP:0003961	decreased lean body mass	Fndc3a<em1(IMPC)Tcp>/Fndc3a<em1(IMPC)Tcp>	C57BL/6N-Fndc3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696741	M	MP:0001925	male infertility	Fndc3a<em1(IMPC)Tcp>/Fndc3a<em1(IMPC)Tcp>	C57BL/6N-Fndc3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696741	F	MP:0010024	increased total body fat amount	Fndc3a<em1(IMPC)Tcp>/Fndc3a<em1(IMPC)Tcp>	C57BL/6N-Fndc3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696741	F	MP:0010097	abnormal retina blood vessel morphology	Fndc3a<em1(IMPC)Tcp>/Fndc3a<em1(IMPC)Tcp>	C57BL/6N-Fndc3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696741	F	MP:0010124	decreased bone mineral content	Fndc3a<em1(IMPC)Tcp>/Fndc3a<em1(IMPC)Tcp>	C57BL/6N-Fndc3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696741	M	MP:0020421	increased freezing behavior	Fndc3a<em1(IMPC)Tcp>/Fndc3a<em1(IMPC)Tcp>	C57BL/6N-Fndc3a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696742	F	MP:0002574	increased vertical activity	Frmd3<em1(IMPC)J>/Frmd3<em1(IMPC)J>	C57BL/6NJ-Frmd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696742	F	MP:0001312	abnormal cornea morphology	Frmd3<em1(IMPC)J>/Frmd3<em1(IMPC)J>	C57BL/6NJ-Frmd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696742	M	MP:0001415	increased exploration in new environment	Frmd3<em1(IMPC)J>/Frmd3<em1(IMPC)J>	C57BL/6NJ-Frmd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696743	M	MP:0001925	male infertility	Fsip1<em1(IMPC)Bay>/Fsip1<em1(IMPC)Bay>	C57BL/6N-Fsip1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6696744	M	MP:0010024	increased total body fat amount	Fyttd1<em1(IMPC)J>/Fyttd1<em1(IMPC)J>	C57BL/6NJ-Fyttd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696744	M	MP:0000367	abnormal coat/ hair morphology	Fyttd1<em1(IMPC)J>/Fyttd1<em1(IMPC)J>	C57BL/6NJ-Fyttd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696744	F	MP:0005562	decreased mean corpuscular hemoglobin	Fyttd1<em1(IMPC)J>/Fyttd1<em1(IMPC)J>	C57BL/6NJ-Fyttd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696744	F	MP:0005553	increased circulating creatinine level	Fyttd1<em1(IMPC)J>/Fyttd1<em1(IMPC)J>	C57BL/6NJ-Fyttd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696744	F	MP:0005343	increased circulating aspartate transaminase level	Fyttd1<em1(IMPC)J>/Fyttd1<em1(IMPC)J>	C57BL/6NJ-Fyttd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696747	F	MP:0002060	abnormal skin morphology	Garem1<em1(IMPC)Mbp>/Garem1<em1(IMPC)Mbp>	C57BL/6N-Garem1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696747	F	MP:0000689	abnormal spleen morphology	Garem1<em1(IMPC)Mbp>/Garem1<em1(IMPC)Mbp>	C57BL/6N-Garem1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696747	F	MP:0000692	small spleen	Garem1<em1(IMPC)Mbp>/Garem1<em1(IMPC)Mbp>	C57BL/6N-Garem1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696747	F	MP:0000601	small liver	Garem1<em1(IMPC)Mbp>/Garem1<em1(IMPC)Mbp>	C57BL/6N-Garem1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696747	F	MP:0002989	small kidney	Garem1<em1(IMPC)Mbp>/Garem1<em1(IMPC)Mbp>	C57BL/6N-Garem1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696747	F	MP:0000598	abnormal liver morphology	Garem1<em1(IMPC)Mbp>/Garem1<em1(IMPC)Mbp>	C57BL/6N-Garem1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696747	F	MP:0002135	abnormal kidney morphology	Garem1<em1(IMPC)Mbp>/Garem1<em1(IMPC)Mbp>	C57BL/6N-Garem1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696750	M	MP:0011886	increased circulating lipase level	Gins2<tm1b(EUCOMM)Wtsi>/Gins2<+>	C57BL/6N-Gins2<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6696752	F	MP:0002792	abnormal retina vasculature morphology	Glyr1<em1(IMPC)Tcp>/Glyr1<+>	C57BL/6N-Glyr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696752	F	MP:0010097	abnormal retina blood vessel morphology	Glyr1<em1(IMPC)Tcp>/Glyr1<+>	C57BL/6N-Glyr1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696753	M	MP:0011874	enlarged urinary bladder	Gm10800<em1(IMPC)Mbp>/Gm10800<em1(IMPC)Mbp>	C57BL/6N-Gm10800<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696753	M	MP:0000538	abnormal urinary bladder morphology	Gm10800<em1(IMPC)Mbp>/Gm10800<em1(IMPC)Mbp>	C57BL/6N-Gm10800<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696753	M	MP:0003068	enlarged kidney	Gm10800<em1(IMPC)Mbp>/Gm10800<em1(IMPC)Mbp>	C57BL/6N-Gm10800<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696753	M	MP:0002339	abnormal lymph node morphology	Gm10800<em1(IMPC)Mbp>/Gm10800<em1(IMPC)Mbp>	C57BL/6N-Gm10800<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696753	M	MP:0000702	enlarged lymph nodes	Gm10800<em1(IMPC)Mbp>/Gm10800<em1(IMPC)Mbp>	C57BL/6N-Gm10800<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696753	M	MP:0002135	abnormal kidney morphology	Gm10800<em1(IMPC)Mbp>/Gm10800<em1(IMPC)Mbp>	C57BL/6N-Gm10800<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696753	F	MP:0001297	microphthalmia	Gm10800<em1(IMPC)Mbp>/Gm10800<em1(IMPC)Mbp>	C57BL/6N-Gm10800<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696753	F	MP:0002092	abnormal eye morphology	Gm10800<em1(IMPC)Mbp>/Gm10800<em1(IMPC)Mbp>	C57BL/6N-Gm10800<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696754	M	MP:0002608	increased hematocrit	Gm5127<em1(IMPC)J>/Y	C57BL/6NJ-Gm5127<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696754	M	MP:0003131	increased erythrocyte cell number	Gm5127<em1(IMPC)J>/Y	C57BL/6NJ-Gm5127<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696754	M	MP:0001552	increased circulating triglyceride level	Gm5127<em1(IMPC)J>/Y	C57BL/6NJ-Gm5127<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696755	F	MP:0004832	enlarged ovary	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696755	M	MP:0001146	abnormal testis morphology	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696755	M	MP:0000599	enlarged liver	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696755	M	MP:0001304	cataract	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696755	F	MP:0000691	enlarged spleen	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696755	F	MP:0002092	abnormal eye morphology	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696755	F	MP:0001126	abnormal ovary morphology	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696755	F	MP:0001297	microphthalmia	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696755	F	MP:0001120	abnormal uterus morphology	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696755	M	MP:0002699	abnormal vitreous body morphology	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696755	F	MP:0000689	abnormal spleen morphology	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696755	F	MP:0004906	enlarged uterus	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696755	F	MP:0000274	enlarged heart	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696755	M	MP:0001148	enlarged testis	Gna15<em1(IMPC)Mbp>/Gna15<em1(IMPC)Mbp>	C57BL/6N-Gna15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696756	F	MP:0002135	abnormal kidney morphology	Gnptg<em1(IMPC)Mbp>/Gnptg<em1(IMPC)Mbp>	C57BL/6N-Gnptg<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696756	M	MP:0005562	decreased mean corpuscular hemoglobin	Gnptg<em1(IMPC)Mbp>/Gnptg<em1(IMPC)Mbp>	C57BL/6N-Gnptg<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696756	F	MP:0005238	increased brain size	Gnptg<em1(IMPC)Mbp>/Gnptg<em1(IMPC)Mbp>	C57BL/6N-Gnptg<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696756	F	MP:0002968	increased circulating alkaline phosphatase level	Gnptg<em1(IMPC)Mbp>/Gnptg<em1(IMPC)Mbp>	C57BL/6N-Gnptg<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696756	F	MP:0002989	small kidney	Gnptg<em1(IMPC)Mbp>/Gnptg<em1(IMPC)Mbp>	C57BL/6N-Gnptg<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696756	M	MP:0010067	increased red blood cell distribution width	Gnptg<em1(IMPC)Mbp>/Gnptg<em1(IMPC)Mbp>	C57BL/6N-Gnptg<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696756	F	MP:0002152	abnormal brain morphology	Gnptg<em1(IMPC)Mbp>/Gnptg<em1(IMPC)Mbp>	C57BL/6N-Gnptg<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696756	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Gnptg<em1(IMPC)Mbp>/Gnptg<em1(IMPC)Mbp>	C57BL/6N-Gnptg<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696757	F	MP:0005560	decreased circulating glucose level	Golt1a<tm1b(KOMP)Wtsi>/Golt1a<tm1b(KOMP)Wtsi>	C57BL/6N-Golt1a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696757	F	MP:0005344	increased circulating bilirubin level	Golt1a<tm1b(KOMP)Wtsi>/Golt1a<tm1b(KOMP)Wtsi>	C57BL/6N-Golt1a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696757	F	MP:0002968	increased circulating alkaline phosphatase level	Golt1a<tm1b(KOMP)Wtsi>/Golt1a<tm1b(KOMP)Wtsi>	C57BL/6N-Golt1a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696757	F	MP:0005561	increased mean corpuscular hemoglobin	Golt1a<tm1b(KOMP)Wtsi>/Golt1a<tm1b(KOMP)Wtsi>	C57BL/6N-Golt1a<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696759	F	MP:0000601	small liver	Gpc1<em1(IMPC)Mbp>/Gpc1<em1(IMPC)Mbp>	C57BL/6N-Gpc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696759	F	MP:0002092	abnormal eye morphology	Gpc1<em1(IMPC)Mbp>/Gpc1<em1(IMPC)Mbp>	C57BL/6N-Gpc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696759	F	MP:0000598	abnormal liver morphology	Gpc1<em1(IMPC)Mbp>/Gpc1<em1(IMPC)Mbp>	C57BL/6N-Gpc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696759	F	MP:0000689	abnormal spleen morphology	Gpc1<em1(IMPC)Mbp>/Gpc1<em1(IMPC)Mbp>	C57BL/6N-Gpc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696759	M	MP:0010067	increased red blood cell distribution width	Gpc1<em1(IMPC)Mbp>/Gpc1<em1(IMPC)Mbp>	C57BL/6N-Gpc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696759	F	MP:0002339	abnormal lymph node morphology	Gpc1<em1(IMPC)Mbp>/Gpc1<em1(IMPC)Mbp>	C57BL/6N-Gpc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696759	M	MP:0002574	increased vertical activity	Gpc1<em1(IMPC)Mbp>/Gpc1<em1(IMPC)Mbp>	C57BL/6N-Gpc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696759	F	MP:0000691	enlarged spleen	Gpc1<em1(IMPC)Mbp>/Gpc1<em1(IMPC)Mbp>	C57BL/6N-Gpc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696759	F	MP:0000702	enlarged lymph nodes	Gpc1<em1(IMPC)Mbp>/Gpc1<em1(IMPC)Mbp>	C57BL/6N-Gpc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696760	F	MP:0002060	abnormal skin morphology	Gpd1<em1(IMPC)Mbp>/Gpd1<em1(IMPC)Mbp>	C57BL/6N-Gpd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696762	F	MP:0000601	small liver	Grik5<em1(IMPC)Mbp>/Grik5<em1(IMPC)Mbp>	C57BL/6N-Grik5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696762	F	MP:0000598	abnormal liver morphology	Grik5<em1(IMPC)Mbp>/Grik5<em1(IMPC)Mbp>	C57BL/6N-Grik5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696762	M	MP:0000689	abnormal spleen morphology	Grik5<em1(IMPC)Mbp>/Grik5<em1(IMPC)Mbp>	C57BL/6N-Grik5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696762	F	MP:0002152	abnormal brain morphology	Grik5<em1(IMPC)Mbp>/Grik5<em1(IMPC)Mbp>	C57BL/6N-Grik5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696762	F	MP:0000774	decreased brain size	Grik5<em1(IMPC)Mbp>/Grik5<em1(IMPC)Mbp>	C57BL/6N-Grik5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696762	F	MP:0001258	decreased body length	Grik5<em1(IMPC)Mbp>/Grik5<em1(IMPC)Mbp>	C57BL/6N-Grik5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696762	M	MP:0002092	abnormal eye morphology	Grik5<em1(IMPC)Mbp>/Grik5<em1(IMPC)Mbp>	C57BL/6N-Grik5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696762	M	MP:0000691	enlarged spleen	Grik5<em1(IMPC)Mbp>/Grik5<em1(IMPC)Mbp>	C57BL/6N-Grik5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696762	F	MP:0002699	abnormal vitreous body morphology	Grik5<em1(IMPC)Mbp>/Grik5<em1(IMPC)Mbp>	C57BL/6N-Grik5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696762	M	MP:0000266	abnormal heart morphology	Grik5<em1(IMPC)Mbp>/Grik5<em1(IMPC)Mbp>	C57BL/6N-Grik5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696762	M	MP:0000274	enlarged heart	Grik5<em1(IMPC)Mbp>/Grik5<em1(IMPC)Mbp>	C57BL/6N-Grik5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696762	M	MP:0001293	anophthalmia	Grik5<em1(IMPC)Mbp>/Grik5<em1(IMPC)Mbp>	C57BL/6N-Grik5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696763	M	MP:0000689	abnormal spleen morphology	Gsr<em1(IMPC)Mbp>/Gsr<em1(IMPC)Mbp>	C57BL/6N-Gsr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696763	M	MP:0000691	enlarged spleen	Gsr<em1(IMPC)Mbp>/Gsr<em1(IMPC)Mbp>	C57BL/6N-Gsr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696763	M	MP:0002135	abnormal kidney morphology	Gsr<em1(IMPC)Mbp>/Gsr<em1(IMPC)Mbp>	C57BL/6N-Gsr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696763	M	MP:0002060	abnormal skin morphology	Gsr<em1(IMPC)Mbp>/Gsr<em1(IMPC)Mbp>	C57BL/6N-Gsr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696763	M	MP:0003068	enlarged kidney	Gsr<em1(IMPC)Mbp>/Gsr<em1(IMPC)Mbp>	C57BL/6N-Gsr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696766	F	MP:0001258	decreased body length	Gys1<em1(IMPC)Bay>/Gys1<+>	C57BL/6N-Gys1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6696769	F	MP:0013278	decreased fasting circulating glucose level	Hadhb<em1(IMPC)Bay>/Hadhb<+>	C57BL/6N-Hadhb<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6696771	F	MP:0005554	decreased circulating creatinine level	Hip1<em1(IMPC)Hmgu>/Hip1<em1(IMPC)Hmgu>	C57BL/6N-Hip1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696771	M	MP:0001312	abnormal cornea morphology	Hip1<em1(IMPC)Hmgu>/Hip1<em1(IMPC)Hmgu>	C57BL/6N-Hip1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696771	M	MP:0001314	cornea opacity	Hip1<em1(IMPC)Hmgu>/Hip1<em1(IMPC)Hmgu>	C57BL/6N-Hip1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696771	M	MP:0010123	increased bone mineral content	Hip1<em1(IMPC)Hmgu>/Hip1<em1(IMPC)Hmgu>	C57BL/6N-Hip1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696771	M	MP:0001258	decreased body length	Hip1<em1(IMPC)Hmgu>/Hip1<em1(IMPC)Hmgu>	C57BL/6N-Hip1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696772	F	MP:0010097	abnormal retina blood vessel morphology	Hook2<em1(IMPC)Tcp>/Hook2<em1(IMPC)Tcp>	C57BL/6N-Hook2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696772	M	MP:0001157	small seminal vesicle	Hook2<em1(IMPC)Tcp>/Hook2<em1(IMPC)Tcp>	C57BL/6N-Hook2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696772	M	MP:0010067	increased red blood cell distribution width	Hook2<em1(IMPC)Tcp>/Hook2<em1(IMPC)Tcp>	C57BL/6N-Hook2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696772	F	MP:0002092	abnormal eye morphology	Hook2<em1(IMPC)Tcp>/Hook2<em1(IMPC)Tcp>	C57BL/6N-Hook2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696772	M	MP:0000702	enlarged lymph nodes	Hook2<em1(IMPC)Tcp>/Hook2<em1(IMPC)Tcp>	C57BL/6N-Hook2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696772	F	MP:0002060	abnormal skin morphology	Hook2<em1(IMPC)Tcp>/Hook2<em1(IMPC)Tcp>	C57BL/6N-Hook2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696772	F	MP:0002792	abnormal retina vasculature morphology	Hook2<em1(IMPC)Tcp>/Hook2<em1(IMPC)Tcp>	C57BL/6N-Hook2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696772	M	MP:0005562	decreased mean corpuscular hemoglobin	Hook2<em1(IMPC)Tcp>/Hook2<em1(IMPC)Tcp>	C57BL/6N-Hook2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696773	F	MP:0000598	abnormal liver morphology	Hoxa4<em1(IMPC)Mbp>/Hoxa4<em1(IMPC)Mbp>	C57BL/6N-Hoxa4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696773	F	MP:0002989	small kidney	Hoxa4<em1(IMPC)Mbp>/Hoxa4<em1(IMPC)Mbp>	C57BL/6N-Hoxa4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696773	F	MP:0001120	abnormal uterus morphology	Hoxa4<em1(IMPC)Mbp>/Hoxa4<em1(IMPC)Mbp>	C57BL/6N-Hoxa4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696773	F	MP:0000601	small liver	Hoxa4<em1(IMPC)Mbp>/Hoxa4<em1(IMPC)Mbp>	C57BL/6N-Hoxa4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696773	F	MP:0002135	abnormal kidney morphology	Hoxa4<em1(IMPC)Mbp>/Hoxa4<em1(IMPC)Mbp>	C57BL/6N-Hoxa4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696774	F	MP:0000221	decreased leukocyte cell number	Hps5<em1(IMPC)J>/Hps5<em1(IMPC)J>	C57BL/6NJ-Hps5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696774	F	MP:0012122	abnormal iris transillumination	Hps5<em1(IMPC)J>/Hps5<em1(IMPC)J>	C57BL/6NJ-Hps5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696775	M	MP:0002965	increased circulating serum albumin level	Ibtk<em1(IMPC)Hmgu>/Ibtk<em1(IMPC)Hmgu>	C57BL/6N-Ibtk<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696776	M	MP:0000774	decreased brain size	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696776	M	MP:0001147	small testis	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696776	F	MP:0010097	abnormal retina blood vessel morphology	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696776	M	MP:0001488	increased startle reflex	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696776	F	MP:0002599	increased mean platelet volume	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696776	F	MP:0002135	abnormal kidney morphology	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696776	F	MP:0000598	abnormal liver morphology	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696776	M	MP:0002590	increased mean corpuscular volume	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696776	F	MP:0004952	increased spleen weight	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696776	M	MP:0002152	abnormal brain morphology	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696776	M	MP:0001146	abnormal testis morphology	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696776	M	MP:0020421	increased freezing behavior	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696776	F	MP:0002989	small kidney	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696776	F	MP:0000601	small liver	Id3<em1(IMPC)Mbp>/Id3<em1(IMPC)Mbp>	C57BL/6N-Id3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696777	F	MP:0002092	abnormal eye morphology	Ifngr1<em1(IMPC)Mbp>/Ifngr1<em1(IMPC)Mbp>	C57BL/6N-Ifngr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696777	F	MP:0002060	abnormal skin morphology	Ifngr1<em1(IMPC)Mbp>/Ifngr1<em1(IMPC)Mbp>	C57BL/6N-Ifngr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696778	F	MP:0000601	small liver	Il17a<em1(IMPC)Mbp>/Il17a<em1(IMPC)Mbp>	C57BL/6N-Il17a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696778	M	MP:0002135	abnormal kidney morphology	Il17a<em1(IMPC)Mbp>/Il17a<em1(IMPC)Mbp>	C57BL/6N-Il17a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696778	M	MP:0002989	small kidney	Il17a<em1(IMPC)Mbp>/Il17a<em1(IMPC)Mbp>	C57BL/6N-Il17a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696778	M	MP:0020421	increased freezing behavior	Il17a<em1(IMPC)Mbp>/Il17a<em1(IMPC)Mbp>	C57BL/6N-Il17a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696778	F	MP:0000689	abnormal spleen morphology	Il17a<em1(IMPC)Mbp>/Il17a<em1(IMPC)Mbp>	C57BL/6N-Il17a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696778	F	MP:0000691	enlarged spleen	Il17a<em1(IMPC)Mbp>/Il17a<em1(IMPC)Mbp>	C57BL/6N-Il17a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696778	F	MP:0000598	abnormal liver morphology	Il17a<em1(IMPC)Mbp>/Il17a<em1(IMPC)Mbp>	C57BL/6N-Il17a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696779	M	MP:0002875	decreased erythrocyte cell number	Il1a<tm1b(EUCOMM)Wtsi>/Il1a<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il1a<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6696779	F	MP:0013278	decreased fasting circulating glucose level	Il1a<tm1b(EUCOMM)Wtsi>/Il1a<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il1a<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6696779	M	MP:0002874	decreased hemoglobin content	Il1a<tm1b(EUCOMM)Wtsi>/Il1a<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il1a<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6696779	M	MP:0000208	decreased hematocrit	Il1a<tm1b(EUCOMM)Wtsi>/Il1a<tm1b(EUCOMM)Wtsi>	C57BL/6N-Il1a<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:6696780	M	MP:0001399	hyperactivity	Il1rl2<em1(IMPC)Mbp>/Il1rl2<em1(IMPC)Mbp>	C57BL/6N-Il1rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696780	M	MP:0004924	abnormal behavior	Il1rl2<em1(IMPC)Mbp>/Il1rl2<em1(IMPC)Mbp>	C57BL/6N-Il1rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696780	M	MP:0001402	decreased locomotor activity	Il1rl2<em1(IMPC)Mbp>/Il1rl2<em1(IMPC)Mbp>	C57BL/6N-Il1rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696780	M	MP:0020870	decreased thigmotaxis	Il1rl2<em1(IMPC)Mbp>/Il1rl2<em1(IMPC)Mbp>	C57BL/6N-Il1rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696780	M	MP:0001364	decreased anxiety-related response	Il1rl2<em1(IMPC)Mbp>/Il1rl2<em1(IMPC)Mbp>	C57BL/6N-Il1rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696781	F	MP:0001293	anophthalmia	Il9r<em1(IMPC)Mbp>/Il9r<em1(IMPC)Mbp>	C57BL/6N-Il9r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696781	F	MP:0000598	abnormal liver morphology	Il9r<em1(IMPC)Mbp>/Il9r<em1(IMPC)Mbp>	C57BL/6N-Il9r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696781	F	MP:0002092	abnormal eye morphology	Il9r<em1(IMPC)Mbp>/Il9r<em1(IMPC)Mbp>	C57BL/6N-Il9r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696781	F	MP:0001258	decreased body length	Il9r<em1(IMPC)Mbp>/Il9r<em1(IMPC)Mbp>	C57BL/6N-Il9r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696781	M	MP:0002699	abnormal vitreous body morphology	Il9r<em1(IMPC)Mbp>/Il9r<em1(IMPC)Mbp>	C57BL/6N-Il9r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696781	M	MP:0004924	abnormal behavior	Il9r<em1(IMPC)Mbp>/Il9r<em1(IMPC)Mbp>	C57BL/6N-Il9r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696781	M	MP:0001304	cataract	Il9r<em1(IMPC)Mbp>/Il9r<em1(IMPC)Mbp>	C57BL/6N-Il9r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696781	M	MP:0002135	abnormal kidney morphology	Il9r<em1(IMPC)Mbp>/Il9r<em1(IMPC)Mbp>	C57BL/6N-Il9r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696781	M	MP:0020870	decreased thigmotaxis	Il9r<em1(IMPC)Mbp>/Il9r<em1(IMPC)Mbp>	C57BL/6N-Il9r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696781	M	MP:0001364	decreased anxiety-related response	Il9r<em1(IMPC)Mbp>/Il9r<em1(IMPC)Mbp>	C57BL/6N-Il9r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696781	M	MP:0002989	small kidney	Il9r<em1(IMPC)Mbp>/Il9r<em1(IMPC)Mbp>	C57BL/6N-Il9r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696781	F	MP:0000601	small liver	Il9r<em1(IMPC)Mbp>/Il9r<em1(IMPC)Mbp>	C57BL/6N-Il9r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696782	F	MP:0005343	increased circulating aspartate transaminase level	Irf6<em1(IMPC)Wtsi>/Irf6<em1(IMPC)Wtsi>	C57BL/6N-Irf6<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696782	F	MP:0010090	increased circulating creatine kinase level	Irf6<em1(IMPC)Wtsi>/Irf6<em1(IMPC)Wtsi>	C57BL/6N-Irf6<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696785	F	MP:0000691	enlarged spleen	Itk<em1(IMPC)Mbp>/Itk<em1(IMPC)Mbp>	C57BL/6N-Itk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696785	F	MP:0000689	abnormal spleen morphology	Itk<em1(IMPC)Mbp>/Itk<em1(IMPC)Mbp>	C57BL/6N-Itk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696786	F	MP:0001258	decreased body length	Itpr3<em1(IMPC)Mbp>/Itpr3<em1(IMPC)Mbp>	C57BL/6N-Itpr3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696786	M	MP:0000689	abnormal spleen morphology	Itpr3<em1(IMPC)Mbp>/Itpr3<em1(IMPC)Mbp>	C57BL/6N-Itpr3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696786	M	MP:0000691	enlarged spleen	Itpr3<em1(IMPC)Mbp>/Itpr3<em1(IMPC)Mbp>	C57BL/6N-Itpr3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696786	F	MP:0001314	cornea opacity	Itpr3<em1(IMPC)Mbp>/Itpr3<em1(IMPC)Mbp>	C57BL/6N-Itpr3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696787	F	MP:0001404	no spontaneous movement	Katnip<em1(IMPC)Mbp>/Katnip<em1(IMPC)Mbp>	C57BL/6NCrl-Katnip<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6696788	M	MP:0001200	thick skin	Kcna5<em1(IMPC)Mbp>/Kcna5<em1(IMPC)Mbp>	C57BL/6N-Kcna5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696789	F	MP:0001785	edema	Kctd3<em1(IMPC)Tcp>/Kctd3<em1(IMPC)Tcp>	C57BL/6N-Kctd3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696790	M	MP:0001399	hyperactivity	Kif13a<em1(IMPC)Mbp>/Kif13a<em1(IMPC)Mbp>	C57BL/6N-Kif13a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696790	F	MP:0009709	hydrometra	Kif13a<em1(IMPC)Mbp>/Kif13a<em1(IMPC)Mbp>	C57BL/6N-Kif13a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696790	F	MP:0002989	small kidney	Kif13a<em1(IMPC)Mbp>/Kif13a<em1(IMPC)Mbp>	C57BL/6N-Kif13a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696790	M	MP:0001148	enlarged testis	Kif13a<em1(IMPC)Mbp>/Kif13a<em1(IMPC)Mbp>	C57BL/6N-Kif13a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696790	M	MP:0001146	abnormal testis morphology	Kif13a<em1(IMPC)Mbp>/Kif13a<em1(IMPC)Mbp>	C57BL/6N-Kif13a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696790	F	MP:0009142	decreased prepulse inhibition	Kif13a<em1(IMPC)Mbp>/Kif13a<em1(IMPC)Mbp>	C57BL/6N-Kif13a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696790	M	MP:0001489	decreased startle reflex	Kif13a<em1(IMPC)Mbp>/Kif13a<em1(IMPC)Mbp>	C57BL/6N-Kif13a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696790	F	MP:0002135	abnormal kidney morphology	Kif13a<em1(IMPC)Mbp>/Kif13a<em1(IMPC)Mbp>	C57BL/6N-Kif13a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696790	M	MP:0002060	abnormal skin morphology	Kif13a<em1(IMPC)Mbp>/Kif13a<em1(IMPC)Mbp>	C57BL/6N-Kif13a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696793	F	MP:0000063	decreased bone mineral density	Klhl9<em1(IMPC)J>/Klhl9<em1(IMPC)J>	C57BL/6NJ-Klhl9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696793	F	MP:0001325	abnormal retina morphology	Klhl9<em1(IMPC)J>/Klhl9<em1(IMPC)J>	C57BL/6NJ-Klhl9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696793	F	MP:0003795	abnormal bone structure	Klhl9<em1(IMPC)J>/Klhl9<em1(IMPC)J>	C57BL/6NJ-Klhl9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696793	F	MP:0010124	decreased bone mineral content	Klhl9<em1(IMPC)J>/Klhl9<em1(IMPC)J>	C57BL/6NJ-Klhl9<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696794	M	MP:0000219	increased neutrophil cell number	Klk4<tm1.1(KOMP)Vlcg>/Klk4<tm1.1(KOMP)Vlcg>	C57BL/6N-Klk4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6696794	M	MP:0002606	increased basophil cell number	Klk4<tm1.1(KOMP)Vlcg>/Klk4<tm1.1(KOMP)Vlcg>	C57BL/6N-Klk4<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6696797	M	MP:0002874	decreased hemoglobin content	Larp4b<em1(IMPC)Wtsi>/Larp4b<em1(IMPC)Wtsi>	C57BL/6N-Larp4b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696797	M	MP:0002079	increased circulating insulin level	Larp4b<em1(IMPC)Wtsi>/Larp4b<em1(IMPC)Wtsi>	C57BL/6N-Larp4b<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696799	F	MP:0000218	increased leukocyte cell number	Lhx5<em1(IMPC)Ccpcz>/Lhx5<+>	C57BL/6N-Lhx5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696799	M	MP:0000266	abnormal heart morphology	Lhx5<em1(IMPC)Ccpcz>/Lhx5<+>	C57BL/6N-Lhx5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696799	M	MP:0001157	small seminal vesicle	Lhx5<em1(IMPC)Ccpcz>/Lhx5<+>	C57BL/6N-Lhx5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696799	F	MP:0002100	abnormal tooth morphology	Lhx5<em1(IMPC)Ccpcz>/Lhx5<+>	C57BL/6N-Lhx5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696799	M	MP:0000274	enlarged heart	Lhx5<em1(IMPC)Ccpcz>/Lhx5<+>	C57BL/6N-Lhx5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696799	F	MP:0000691	enlarged spleen	Lhx5<em1(IMPC)Ccpcz>/Lhx5<+>	C57BL/6N-Lhx5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696799	F	MP:0000689	abnormal spleen morphology	Lhx5<em1(IMPC)Ccpcz>/Lhx5<+>	C57BL/6N-Lhx5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696799	M	MP:0002059	abnormal seminal vesicle morphology	Lhx5<em1(IMPC)Ccpcz>/Lhx5<+>	C57BL/6N-Lhx5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696802	F	MP:0002968	increased circulating alkaline phosphatase level	Loxl4<tm1.1(KOMP)Vlcg>/Loxl4<tm1.1(KOMP)Vlcg>	C57BL/6N-Loxl4<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6696802	F	MP:0001399	hyperactivity	Loxl4<tm1.1(KOMP)Vlcg>/Loxl4<tm1.1(KOMP)Vlcg>	C57BL/6N-Loxl4<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6696803	M	MP:0001147	small testis	Lrfn3<tm1.1(KOMP)Vlcg>/Lrfn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Lrfn3<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6696803	M	MP:0001146	abnormal testis morphology	Lrfn3<tm1.1(KOMP)Vlcg>/Lrfn3<tm1.1(KOMP)Vlcg>	C57BL/6N-Lrfn3<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6696809	M	MP:0005293	impaired glucose tolerance	Lyar<em1(IMPC)J>/Lyar<em1(IMPC)J>	C57BL/6NJ-Lyar<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696809	F	MP:0005343	increased circulating aspartate transaminase level	Lyar<em1(IMPC)J>/Lyar<em1(IMPC)J>	C57BL/6NJ-Lyar<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696810	F	MP:0002092	abnormal eye morphology	Malrd1<em1(IMPC)Mbp>/Malrd1<em1(IMPC)Mbp>	C57BL/6N-Malrd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696810	F	MP:0000601	small liver	Malrd1<em1(IMPC)Mbp>/Malrd1<em1(IMPC)Mbp>	C57BL/6N-Malrd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696810	F	MP:0000598	abnormal liver morphology	Malrd1<em1(IMPC)Mbp>/Malrd1<em1(IMPC)Mbp>	C57BL/6N-Malrd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696810	F	MP:0001293	anophthalmia	Malrd1<em1(IMPC)Mbp>/Malrd1<em1(IMPC)Mbp>	C57BL/6N-Malrd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696811	M	MP:0002135	abnormal kidney morphology	Map3k9<em1(IMPC)Mbp>/Map3k9<+>	C57BL/6N-Map3k9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696811	M	MP:0002989	small kidney	Map3k9<em1(IMPC)Mbp>/Map3k9<+>	C57BL/6N-Map3k9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696812	M	MP:0000219	increased neutrophil cell number	Map3k9<em1(IMPC)Mbp>/Map3k9<em1(IMPC)Mbp>	C57BL/6N-Map3k9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696812	M	MP:0001148	enlarged testis	Map3k9<em1(IMPC)Mbp>/Map3k9<em1(IMPC)Mbp>	C57BL/6N-Map3k9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696812	M	MP:0001146	abnormal testis morphology	Map3k9<em1(IMPC)Mbp>/Map3k9<em1(IMPC)Mbp>	C57BL/6N-Map3k9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696812	F	MP:0002060	abnormal skin morphology	Map3k9<em1(IMPC)Mbp>/Map3k9<em1(IMPC)Mbp>	C57BL/6N-Map3k9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696812	F	MP:0006203	eye hemorrhage	Map3k9<em1(IMPC)Mbp>/Map3k9<em1(IMPC)Mbp>	C57BL/6N-Map3k9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696813	F	MP:0010052	increased grip strength	Mbip<em1(IMPC)J>/Mbip<+>	C57BL/6NJ-Mbip<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696815	M	MP:0001146	abnormal testis morphology	Mc3r<em1(IMPC)Mbp>/Mc3r<em1(IMPC)Mbp>	C57BL/6N-Mc3r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696815	F	MP:0002135	abnormal kidney morphology	Mc3r<em1(IMPC)Mbp>/Mc3r<em1(IMPC)Mbp>	C57BL/6N-Mc3r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696815	M	MP:0002060	abnormal skin morphology	Mc3r<em1(IMPC)Mbp>/Mc3r<em1(IMPC)Mbp>	C57BL/6N-Mc3r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696815	M	MP:0001147	small testis	Mc3r<em1(IMPC)Mbp>/Mc3r<em1(IMPC)Mbp>	C57BL/6N-Mc3r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696815	F	MP:0010024	increased total body fat amount	Mc3r<em1(IMPC)Mbp>/Mc3r<em1(IMPC)Mbp>	C57BL/6N-Mc3r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696815	F	MP:0002834	decreased heart weight	Mc3r<em1(IMPC)Mbp>/Mc3r<em1(IMPC)Mbp>	C57BL/6N-Mc3r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696815	F	MP:0002989	small kidney	Mc3r<em1(IMPC)Mbp>/Mc3r<em1(IMPC)Mbp>	C57BL/6N-Mc3r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696818	M	MP:0003960	increased lean body mass	Med23<em1(IMPC)Wtsi>/Med23<+>	C57BL/6N-Med23<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696818	F	MP:0001556	increased circulating HDL cholesterol level	Med23<em1(IMPC)Wtsi>/Med23<+>	C57BL/6N-Med23<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696818	F	MP:0010124	decreased bone mineral content	Med23<em1(IMPC)Wtsi>/Med23<+>	C57BL/6N-Med23<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696819	F	MP:0002060	abnormal skin morphology	Mrap<em1(IMPC)Tcp>/Mrap<+>	C57BL/6N-Mrap<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696819	F	MP:0000157	abnormal sternum morphology	Mrap<em1(IMPC)Tcp>/Mrap<+>	C57BL/6N-Mrap<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696820	M	MP:0002060	abnormal skin morphology	Mrgprx1<em1(IMPC)Tcp>/Mrgprx1<em1(IMPC)Tcp>	C57BL/6N-Mrgprx1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696821	F	MP:0001402	decreased locomotor activity	Mrpl41<em1(IMPC)Bay>/Mrpl41<+>	C57BL/6N-Mrpl41<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6696823	M	MP:0001489	decreased startle reflex	Muc5b<em1(IMPC)Mbp>/Muc5b<em1(IMPC)Mbp>	C57BL/6N-Muc5b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696823	F	MP:0000601	small liver	Muc5b<em1(IMPC)Mbp>/Muc5b<em1(IMPC)Mbp>	C57BL/6N-Muc5b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696823	F	MP:0002060	abnormal skin morphology	Muc5b<em1(IMPC)Mbp>/Muc5b<em1(IMPC)Mbp>	C57BL/6N-Muc5b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696823	F	MP:0000598	abnormal liver morphology	Muc5b<em1(IMPC)Mbp>/Muc5b<em1(IMPC)Mbp>	C57BL/6N-Muc5b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696824	M	MP:0010053	decreased grip strength	Mydgf<em1(IMPC)Hmgu>/Mydgf<em1(IMPC)Hmgu>	C57BL/6N-Mydgf<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696825	F	MP:0005343	increased circulating aspartate transaminase level	Mynn<em1(IMPC)J>/Mynn<em1(IMPC)J>	C57BL/6NJ-Mynn<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696825	F	MP:0001289	persistence of hyaloid vascular system	Mynn<em1(IMPC)J>/Mynn<em1(IMPC)J>	C57BL/6NJ-Mynn<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696826	F	MP:0002989	small kidney	Myom3<em1(IMPC)Mbp>/Myom3<em1(IMPC)Mbp>	C57BL/6N-Myom3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696826	F	MP:0002135	abnormal kidney morphology	Myom3<em1(IMPC)Mbp>/Myom3<em1(IMPC)Mbp>	C57BL/6N-Myom3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696828	M	MP:0000774	decreased brain size	Nav1<em1(IMPC)Mbp>/Nav1<em1(IMPC)Mbp>	C57BL/6N-Nav1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696828	M	MP:0020421	increased freezing behavior	Nav1<em1(IMPC)Mbp>/Nav1<em1(IMPC)Mbp>	C57BL/6N-Nav1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696828	M	MP:0002060	abnormal skin morphology	Nav1<em1(IMPC)Mbp>/Nav1<em1(IMPC)Mbp>	C57BL/6N-Nav1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696828	M	MP:0002152	abnormal brain morphology	Nav1<em1(IMPC)Mbp>/Nav1<em1(IMPC)Mbp>	C57BL/6N-Nav1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696828	F	MP:0002135	abnormal kidney morphology	Nav1<em1(IMPC)Mbp>/Nav1<em1(IMPC)Mbp>	C57BL/6N-Nav1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696828	F	MP:0010506	prolonged RR interval	Nav1<em1(IMPC)Mbp>/Nav1<em1(IMPC)Mbp>	C57BL/6N-Nav1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696828	M	MP:0000689	abnormal spleen morphology	Nav1<em1(IMPC)Mbp>/Nav1<em1(IMPC)Mbp>	C57BL/6N-Nav1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696828	F	MP:0002989	small kidney	Nav1<em1(IMPC)Mbp>/Nav1<em1(IMPC)Mbp>	C57BL/6N-Nav1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696828	F	MP:0005333	decreased heart rate	Nav1<em1(IMPC)Mbp>/Nav1<em1(IMPC)Mbp>	C57BL/6N-Nav1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696828	M	MP:0000691	enlarged spleen	Nav1<em1(IMPC)Mbp>/Nav1<em1(IMPC)Mbp>	C57BL/6N-Nav1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696829	F	MP:0001289	persistence of hyaloid vascular system	Ncor2<em1(IMPC)Mbp>/Ncor2<+>	C57BL/6N-Ncor2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696830	F	MP:0000195	decreased circulating calcium level	Necap2<em1(IMPC)J>/Necap2<em1(IMPC)J>	C57BL/6NJ-Necap2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696831	F	MP:0002792	abnormal retina vasculature morphology	Nifk<em1(IMPC)Mbp>/Nifk<+>	C57BL/6N-Nifk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696831	M	MP:0001289	persistence of hyaloid vascular system	Nifk<em1(IMPC)Mbp>/Nifk<+>	C57BL/6N-Nifk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696831	F	MP:0001325	abnormal retina morphology	Nifk<em1(IMPC)Mbp>/Nifk<+>	C57BL/6N-Nifk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696831	F	MP:0001304	cataract	Nifk<em1(IMPC)Mbp>/Nifk<+>	C57BL/6N-Nifk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696831	F	MP:0002092	abnormal eye morphology	Nifk<em1(IMPC)Mbp>/Nifk<+>	C57BL/6N-Nifk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696831	F	MP:0002699	abnormal vitreous body morphology	Nifk<em1(IMPC)Mbp>/Nifk<+>	C57BL/6N-Nifk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696831	F	MP:0001293	anophthalmia	Nifk<em1(IMPC)Mbp>/Nifk<+>	C57BL/6N-Nifk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696833	F	MP:0000266	abnormal heart morphology	Nlrp1a<em1(IMPC)Mbp>/Nlrp1a<em1(IMPC)Mbp>	C57BL/6N-Nlrp1a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696833	F	MP:0001297	microphthalmia	Nlrp1a<em1(IMPC)Mbp>/Nlrp1a<em1(IMPC)Mbp>	C57BL/6N-Nlrp1a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696833	F	MP:0002092	abnormal eye morphology	Nlrp1a<em1(IMPC)Mbp>/Nlrp1a<em1(IMPC)Mbp>	C57BL/6N-Nlrp1a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696833	F	MP:0000274	enlarged heart	Nlrp1a<em1(IMPC)Mbp>/Nlrp1a<em1(IMPC)Mbp>	C57BL/6N-Nlrp1a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696834	F	MP:0001399	hyperactivity	Nol4<em1(IMPC)J>/Nol4<em1(IMPC)J>	C57BL/6NJ-Nol4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696834	M	MP:0020870	decreased thigmotaxis	Nol4<em1(IMPC)J>/Nol4<em1(IMPC)J>	C57BL/6NJ-Nol4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696834	M	MP:0001364	decreased anxiety-related response	Nol4<em1(IMPC)J>/Nol4<em1(IMPC)J>	C57BL/6NJ-Nol4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696835	M	MP:0002644	decreased circulating triglyceride level	Npcd<em1(IMPC)J>/Npcd<em1(IMPC)J>	C57BL/6NJ-Npcd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696835	F	MP:0002574	increased vertical activity	Npcd<em1(IMPC)J>/Npcd<em1(IMPC)J>	C57BL/6NJ-Npcd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696835	F	MP:0001399	hyperactivity	Npcd<em1(IMPC)J>/Npcd<em1(IMPC)J>	C57BL/6NJ-Npcd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696838	F	MP:0005560	decreased circulating glucose level	Nudcd3<em1(IMPC)Wtsi>/Nudcd3<em1(IMPC)Wtsi>	C57BL/6N-Nudcd3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696838	F	MP:0002079	increased circulating insulin level	Nudcd3<em1(IMPC)Wtsi>/Nudcd3<em1(IMPC)Wtsi>	C57BL/6N-Nudcd3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696838	F	MP:0005565	increased blood urea nitrogen level	Nudcd3<em1(IMPC)Wtsi>/Nudcd3<em1(IMPC)Wtsi>	C57BL/6N-Nudcd3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696838	F	MP:0010067	increased red blood cell distribution width	Nudcd3<em1(IMPC)Wtsi>/Nudcd3<em1(IMPC)Wtsi>	C57BL/6N-Nudcd3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696838	F	MP:0005553	increased circulating creatinine level	Nudcd3<em1(IMPC)Wtsi>/Nudcd3<em1(IMPC)Wtsi>	C57BL/6N-Nudcd3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696839	F	MP:0001697	abnormal embryo size	Nufip2<em1(IMPC)J>/Nufip2<em1(IMPC)J>	C57BL/6NJ-Nufip2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696839	F	MP:0003720	abnormal neural tube closure	Nufip2<em1(IMPC)J>/Nufip2<em1(IMPC)J>	C57BL/6NJ-Nufip2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696840	F	MP:0000601	small liver	Oprl1<em1(IMPC)Mbp>/Oprl1<em1(IMPC)Mbp>	C57BL/6N-Oprl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696840	M	MP:0010067	increased red blood cell distribution width	Oprl1<em1(IMPC)Mbp>/Oprl1<em1(IMPC)Mbp>	C57BL/6N-Oprl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696840	M	MP:0000691	enlarged spleen	Oprl1<em1(IMPC)Mbp>/Oprl1<em1(IMPC)Mbp>	C57BL/6N-Oprl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696840	F	MP:0002092	abnormal eye morphology	Oprl1<em1(IMPC)Mbp>/Oprl1<em1(IMPC)Mbp>	C57BL/6N-Oprl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696840	F	MP:0005562	decreased mean corpuscular hemoglobin	Oprl1<em1(IMPC)Mbp>/Oprl1<em1(IMPC)Mbp>	C57BL/6N-Oprl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696840	F	MP:0002599	increased mean platelet volume	Oprl1<em1(IMPC)Mbp>/Oprl1<em1(IMPC)Mbp>	C57BL/6N-Oprl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696840	F	MP:0001297	microphthalmia	Oprl1<em1(IMPC)Mbp>/Oprl1<em1(IMPC)Mbp>	C57BL/6N-Oprl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696841	M	MP:0000689	abnormal spleen morphology	Pabpc5<em1(IMPC)Mbp>/Y	C57BL/6N-Pabpc5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696841	M	MP:0002060	abnormal skin morphology	Pabpc5<em1(IMPC)Mbp>/Y	C57BL/6N-Pabpc5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696841	M	MP:0000691	enlarged spleen	Pabpc5<em1(IMPC)Mbp>/Y	C57BL/6N-Pabpc5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696842	F	MP:0000601	small liver	Pank1<em1(IMPC)Mbp>/Pank1<em1(IMPC)Mbp>	C57BL/6N-Pank1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696842	F	MP:0000598	abnormal liver morphology	Pank1<em1(IMPC)Mbp>/Pank1<em1(IMPC)Mbp>	C57BL/6N-Pank1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696843	M	MP:0002699	abnormal vitreous body morphology	Parp4<em1(IMPC)Mbp>/Parp4<em1(IMPC)Mbp>	C57BL/6N-Parp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696843	F	MP:0002135	abnormal kidney morphology	Parp4<em1(IMPC)Mbp>/Parp4<em1(IMPC)Mbp>	C57BL/6N-Parp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696843	M	MP:0001417	decreased exploration in new environment	Parp4<em1(IMPC)Mbp>/Parp4<em1(IMPC)Mbp>	C57BL/6N-Parp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696843	F	MP:0002989	small kidney	Parp4<em1(IMPC)Mbp>/Parp4<em1(IMPC)Mbp>	C57BL/6N-Parp4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696844	M	MP:0001314	cornea opacity	Pax6<em1(IMPC)Mbp>/Pax6<+>	C57BL/6N-Pax6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696844	M	MP:0002152	abnormal brain morphology	Pax6<em1(IMPC)Mbp>/Pax6<+>	C57BL/6N-Pax6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696844	F	MP:0001293	anophthalmia	Pax6<em1(IMPC)Mbp>/Pax6<+>	C57BL/6N-Pax6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696844	F	MP:0000601	small liver	Pax6<em1(IMPC)Mbp>/Pax6<+>	C57BL/6N-Pax6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696844	F	MP:0000598	abnormal liver morphology	Pax6<em1(IMPC)Mbp>/Pax6<+>	C57BL/6N-Pax6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696845	M	MP:0011886	increased circulating lipase level	Pcdhgb2<em1(IMPC)Hmgu>/Pcdhgb2<em1(IMPC)Hmgu>	C57BL/6N-Pcdhgb2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696846	F	MP:0000601	small liver	Pdcd7<em1(IMPC)Mbp>/Pdcd7<+>	C57BL/6N-Pdcd7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696846	M	MP:0010507	shortened RR interval	Pdcd7<em1(IMPC)Mbp>/Pdcd7<+>	C57BL/6N-Pdcd7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696846	M	MP:0010067	increased red blood cell distribution width	Pdcd7<em1(IMPC)Mbp>/Pdcd7<+>	C57BL/6N-Pdcd7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696846	F	MP:0000691	enlarged spleen	Pdcd7<em1(IMPC)Mbp>/Pdcd7<+>	C57BL/6N-Pdcd7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696846	F	MP:0000598	abnormal liver morphology	Pdcd7<em1(IMPC)Mbp>/Pdcd7<+>	C57BL/6N-Pdcd7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696846	F	MP:0000689	abnormal spleen morphology	Pdcd7<em1(IMPC)Mbp>/Pdcd7<+>	C57BL/6N-Pdcd7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696846	M	MP:0001157	small seminal vesicle	Pdcd7<em1(IMPC)Mbp>/Pdcd7<+>	C57BL/6N-Pdcd7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696846	M	MP:0001148	enlarged testis	Pdcd7<em1(IMPC)Mbp>/Pdcd7<+>	C57BL/6N-Pdcd7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696846	M	MP:0002626	increased heart rate	Pdcd7<em1(IMPC)Mbp>/Pdcd7<+>	C57BL/6N-Pdcd7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696846	M	MP:0005419	decreased circulating serum albumin level	Pdcd7<em1(IMPC)Mbp>/Pdcd7<+>	C57BL/6N-Pdcd7<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696848	M	MP:0001322	abnormal iris morphology	Pex6<em1(IMPC)Tcp>/Pex6<+>	C57BL/6N-Pex6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696848	M	MP:0006243	impaired pupillary reflex	Pex6<em1(IMPC)Tcp>/Pex6<+>	C57BL/6N-Pex6<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696849	M	MP:0001148	enlarged testis	Pfkm<em1(IMPC)Mbp>/Pfkm<+>	C57BL/6N-Pfkm<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696849	M	MP:0001146	abnormal testis morphology	Pfkm<em1(IMPC)Mbp>/Pfkm<+>	C57BL/6N-Pfkm<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696849	F	MP:0000598	abnormal liver morphology	Pfkm<em1(IMPC)Mbp>/Pfkm<+>	C57BL/6N-Pfkm<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696849	F	MP:0001304	cataract	Pfkm<em1(IMPC)Mbp>/Pfkm<+>	C57BL/6N-Pfkm<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696849	F	MP:0002060	abnormal skin morphology	Pfkm<em1(IMPC)Mbp>/Pfkm<+>	C57BL/6N-Pfkm<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696849	M	MP:0003960	increased lean body mass	Pfkm<em1(IMPC)Mbp>/Pfkm<+>	C57BL/6N-Pfkm<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696849	F	MP:0002699	abnormal vitreous body morphology	Pfkm<em1(IMPC)Mbp>/Pfkm<+>	C57BL/6N-Pfkm<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696849	M	MP:0010025	decreased total body fat amount	Pfkm<em1(IMPC)Mbp>/Pfkm<+>	C57BL/6N-Pfkm<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696849	M	MP:0002059	abnormal seminal vesicle morphology	Pfkm<em1(IMPC)Mbp>/Pfkm<+>	C57BL/6N-Pfkm<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696849	F	MP:0001258	decreased body length	Pfkm<em1(IMPC)Mbp>/Pfkm<+>	C57BL/6N-Pfkm<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696849	F	MP:0000601	small liver	Pfkm<em1(IMPC)Mbp>/Pfkm<+>	C57BL/6N-Pfkm<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696849	M	MP:0001157	small seminal vesicle	Pfkm<em1(IMPC)Mbp>/Pfkm<+>	C57BL/6N-Pfkm<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696851	F	MP:0002966	decreased circulating alkaline phosphatase level	Phf14<em1(IMPC)Hmgu>/Phf14<+>	C57BL/6N-Phf14<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696851	M	MP:0001489	decreased startle reflex	Phf14<em1(IMPC)Hmgu>/Phf14<+>	C57BL/6N-Phf14<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696853	F	MP:0001556	increased circulating HDL cholesterol level	Phf8<em2(IMPC)Wtsi>/Phf8<em2(IMPC)Wtsi>	C57BL/6N-Phf8<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696853	F	MP:0005561	increased mean corpuscular hemoglobin	Phf8<em2(IMPC)Wtsi>/Phf8<em2(IMPC)Wtsi>	C57BL/6N-Phf8<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696853	F	MP:0005178	increased circulating cholesterol level	Phf8<em2(IMPC)Wtsi>/Phf8<em2(IMPC)Wtsi>	C57BL/6N-Phf8<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696853	F	MP:0000182	increased circulating LDL cholesterol level	Phf8<em2(IMPC)Wtsi>/Phf8<em2(IMPC)Wtsi>	C57BL/6N-Phf8<em2(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696854	M	MP:0002792	abnormal retina vasculature morphology	Phlpp1<em1(IMPC)Bay>/Phlpp1<em1(IMPC)Bay>	C57BL/6N-Phlpp1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6696854	F	MP:0003731	abnormal retina outer nuclear layer morphology	Phlpp1<em1(IMPC)Bay>/Phlpp1<em1(IMPC)Bay>	C57BL/6N-Phlpp1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6696855	F	MP:0002092	abnormal eye morphology	Pign<em1(IMPC)Mbp>/Pign<+>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696855	M	MP:0001148	enlarged testis	Pign<em1(IMPC)Mbp>/Pign<+>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696855	F	MP:0001325	abnormal retina morphology	Pign<em1(IMPC)Mbp>/Pign<+>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696855	F	MP:0002060	abnormal skin morphology	Pign<em1(IMPC)Mbp>/Pign<+>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696855	F	MP:0002699	abnormal vitreous body morphology	Pign<em1(IMPC)Mbp>/Pign<+>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696855	M	MP:0001399	hyperactivity	Pign<em1(IMPC)Mbp>/Pign<+>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696855	F	MP:0002989	small kidney	Pign<em1(IMPC)Mbp>/Pign<+>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696855	F	MP:0000601	small liver	Pign<em1(IMPC)Mbp>/Pign<+>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696855	F	MP:0000689	abnormal spleen morphology	Pign<em1(IMPC)Mbp>/Pign<+>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696855	M	MP:0001146	abnormal testis morphology	Pign<em1(IMPC)Mbp>/Pign<+>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696855	F	MP:0000691	enlarged spleen	Pign<em1(IMPC)Mbp>/Pign<+>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696855	F	MP:0000598	abnormal liver morphology	Pign<em1(IMPC)Mbp>/Pign<+>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696855	F	MP:0002135	abnormal kidney morphology	Pign<em1(IMPC)Mbp>/Pign<+>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696858	F	MP:0001399	hyperactivity	Plcb1<em1(IMPC)Mbp>/Plcb1<+>	C57BL/6N-Plcb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696858	F	MP:0002092	abnormal eye morphology	Plcb1<em1(IMPC)Mbp>/Plcb1<+>	C57BL/6N-Plcb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696858	F	MP:0001126	abnormal ovary morphology	Plcb1<em1(IMPC)Mbp>/Plcb1<+>	C57BL/6N-Plcb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696858	M	MP:0000598	abnormal liver morphology	Plcb1<em1(IMPC)Mbp>/Plcb1<+>	C57BL/6N-Plcb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696858	F	MP:0001297	microphthalmia	Plcb1<em1(IMPC)Mbp>/Plcb1<+>	C57BL/6N-Plcb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696858	M	MP:0002060	abnormal skin morphology	Plcb1<em1(IMPC)Mbp>/Plcb1<+>	C57BL/6N-Plcb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696858	M	MP:0003068	enlarged kidney	Plcb1<em1(IMPC)Mbp>/Plcb1<+>	C57BL/6N-Plcb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696858	M	MP:0002135	abnormal kidney morphology	Plcb1<em1(IMPC)Mbp>/Plcb1<+>	C57BL/6N-Plcb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696859	F	MP:0005013	increased lymphocyte cell number	Pld4<em1(IMPC)Mbp>/Pld4<em1(IMPC)Mbp>	C57BL/6N-Pld4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696859	F	MP:0000218	increased leukocyte cell number	Pld4<em1(IMPC)Mbp>/Pld4<em1(IMPC)Mbp>	C57BL/6N-Pld4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696859	F	MP:0004952	increased spleen weight	Pld4<em1(IMPC)Mbp>/Pld4<em1(IMPC)Mbp>	C57BL/6N-Pld4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696859	F	MP:0000220	increased monocyte cell number	Pld4<em1(IMPC)Mbp>/Pld4<em1(IMPC)Mbp>	C57BL/6N-Pld4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696860	M	MP:0000221	decreased leukocyte cell number	Plekhg2<em1(IMPC)J>/Plekhg2<em1(IMPC)J>	C57BL/6NJ-Plekhg2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696860	M	MP:0001566	increased circulating phosphate level	Plekhg2<em1(IMPC)J>/Plekhg2<em1(IMPC)J>	C57BL/6NJ-Plekhg2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696861	M	MP:0001489	decreased startle reflex	Plscr5<em1(IMPC)J>/Plscr5<em1(IMPC)J>	C57BL/6NJ-Plscr5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696863	F	MP:0002989	small kidney	Pof1b<em1(IMPC)Mbp>/Pof1b<em1(IMPC)Mbp>	C57BL/6N-Pof1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696863	F	MP:0000194	increased circulating calcium level	Pof1b<em1(IMPC)Mbp>/Pof1b<em1(IMPC)Mbp>	C57BL/6N-Pof1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696863	F	MP:0000601	small liver	Pof1b<em1(IMPC)Mbp>/Pof1b<em1(IMPC)Mbp>	C57BL/6N-Pof1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696863	F	MP:0002060	abnormal skin morphology	Pof1b<em1(IMPC)Mbp>/Pof1b<em1(IMPC)Mbp>	C57BL/6N-Pof1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696863	F	MP:0000598	abnormal liver morphology	Pof1b<em1(IMPC)Mbp>/Pof1b<em1(IMPC)Mbp>	C57BL/6N-Pof1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696863	F	MP:0002135	abnormal kidney morphology	Pof1b<em1(IMPC)Mbp>/Pof1b<em1(IMPC)Mbp>	C57BL/6N-Pof1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696866	M	MP:0005562	decreased mean corpuscular hemoglobin	Ppie<em1(IMPC)Tcp>/Ppie<+>	C57BL/6N-Ppie<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696866	M	MP:0001417	decreased exploration in new environment	Ppie<em1(IMPC)Tcp>/Ppie<+>	C57BL/6N-Ppie<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696866	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Ppie<em1(IMPC)Tcp>/Ppie<+>	C57BL/6N-Ppie<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696866	F	MP:0003019	increased circulating chloride level	Ppie<em1(IMPC)Tcp>/Ppie<+>	C57BL/6N-Ppie<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696866	F	MP:0005567	decreased circulating total protein level	Ppie<em1(IMPC)Tcp>/Ppie<+>	C57BL/6N-Ppie<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696868	M	MP:0002834	decreased heart weight	Ppp1r12b<em1(IMPC)J>/Ppp1r12b<em1(IMPC)J>	C57BL/6NJ-Ppp1r12b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696868	M	MP:0001284	absent vibrissae	Ppp1r12b<em1(IMPC)J>/Ppp1r12b<em1(IMPC)J>	C57BL/6NJ-Ppp1r12b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696868	F	MP:0001260	increased body weight	Ppp1r12b<em1(IMPC)J>/Ppp1r12b<em1(IMPC)J>	C57BL/6NJ-Ppp1r12b<em1(IMPC)J>/Mmjax	N	36889588
MGI:6696868	M	MP:0000367	abnormal coat/ hair morphology	Ppp1r12b<em1(IMPC)J>/Ppp1r12b<em1(IMPC)J>	C57BL/6NJ-Ppp1r12b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696869	M	MP:0000692	small spleen	Prdm8<em1(IMPC)Wtsi>/Prdm8<+>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696869	M	MP:0002059	abnormal seminal vesicle morphology	Prdm8<em1(IMPC)Wtsi>/Prdm8<+>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696869	M	MP:0002100	abnormal tooth morphology	Prdm8<em1(IMPC)Wtsi>/Prdm8<+>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696869	M	MP:0000689	abnormal spleen morphology	Prdm8<em1(IMPC)Wtsi>/Prdm8<+>	C57BL/6N-Prdm8<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696870	F	MP:0005343	increased circulating aspartate transaminase level	Prkd3<tm1b(EUCOMM)Wtsi>/Prkd3<+>	C57BL/6N-Prkd3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6696870	F	MP:0010097	abnormal retina blood vessel morphology	Prkd3<tm1b(EUCOMM)Wtsi>/Prkd3<+>	C57BL/6N-Prkd3<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6696872	M	MP:0005333	decreased heart rate	Ptpn18<em1(IMPC)J>/Ptpn18<em1(IMPC)J>	C57BL/6NJ-Ptpn18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696872	M	MP:0010506	prolonged RR interval	Ptpn18<em1(IMPC)J>/Ptpn18<em1(IMPC)J>	C57BL/6NJ-Ptpn18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696873	F	MP:0001297	microphthalmia	Pvrig<em1(IMPC)Mbp>/Pvrig<em1(IMPC)Mbp>	C57BL/6N-Pvrig<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696873	F	MP:0002092	abnormal eye morphology	Pvrig<em1(IMPC)Mbp>/Pvrig<em1(IMPC)Mbp>	C57BL/6N-Pvrig<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696873	M	MP:0002339	abnormal lymph node morphology	Pvrig<em1(IMPC)Mbp>/Pvrig<em1(IMPC)Mbp>	C57BL/6N-Pvrig<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696873	M	MP:0000702	enlarged lymph nodes	Pvrig<em1(IMPC)Mbp>/Pvrig<em1(IMPC)Mbp>	C57BL/6N-Pvrig<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696874	M	MP:0003961	decreased lean body mass	Pxk<em1(IMPC)Tcp>/Pxk<em1(IMPC)Tcp>	C57BL/6N-Pxk<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696874	M	MP:0010024	increased total body fat amount	Pxk<em1(IMPC)Tcp>/Pxk<em1(IMPC)Tcp>	C57BL/6N-Pxk<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696874	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Pxk<em1(IMPC)Tcp>/Pxk<em1(IMPC)Tcp>	C57BL/6N-Pxk<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696874	M	MP:0002060	abnormal skin morphology	Pxk<em1(IMPC)Tcp>/Pxk<em1(IMPC)Tcp>	C57BL/6N-Pxk<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696874	M	MP:0010123	increased bone mineral content	Pxk<em1(IMPC)Tcp>/Pxk<em1(IMPC)Tcp>	C57BL/6N-Pxk<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696877	M	MP:0005650	abnormal limb bud morphology	Rexo1<em1(IMPC)J>/Rexo1<em1(IMPC)J>	C57BL/6NJ-Rexo1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696877	F	MP:0011495	abnormal head shape	Rexo1<em1(IMPC)J>/Rexo1<em1(IMPC)J>	C57BL/6NJ-Rexo1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696877	M	MP:0000266	abnormal heart morphology	Rexo1<em1(IMPC)J>/Rexo1<em1(IMPC)J>	C57BL/6NJ-Rexo1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696877	M	MP:0000603	pale liver	Rexo1<em1(IMPC)J>/Rexo1<em1(IMPC)J>	C57BL/6NJ-Rexo1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696879	F	MP:0012121	sclerocornea	Rfxap<em1(IMPC)J>/Rfxap<em1(IMPC)J>	C57BL/6NJ-Rfxap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696879	F	MP:0005287	narrow eye opening	Rfxap<em1(IMPC)J>/Rfxap<em1(IMPC)J>	C57BL/6NJ-Rfxap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696879	F	MP:0001314	cornea opacity	Rfxap<em1(IMPC)J>/Rfxap<em1(IMPC)J>	C57BL/6NJ-Rfxap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696879	F	MP:0005542	cornea vascularization	Rfxap<em1(IMPC)J>/Rfxap<em1(IMPC)J>	C57BL/6NJ-Rfxap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696882	M	MP:0004609	vertebral fusion	Rnf168<tm2b(EUCOMM)Hmgu>/Rnf168<tm2b(EUCOMM)Hmgu>	C57BL/6N-Rnf168<tm2b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6696882	F	MP:0000208	decreased hematocrit	Rnf168<tm2b(EUCOMM)Hmgu>/Rnf168<tm2b(EUCOMM)Hmgu>	C57BL/6N-Rnf168<tm2b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6696882	F	MP:0005011	increased eosinophil cell number	Rnf168<tm2b(EUCOMM)Hmgu>/Rnf168<tm2b(EUCOMM)Hmgu>	C57BL/6N-Rnf168<tm2b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6696882	M	MP:0000266	abnormal heart morphology	Rnf168<tm2b(EUCOMM)Hmgu>/Rnf168<tm2b(EUCOMM)Hmgu>	C57BL/6N-Rnf168<tm2b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6696882	F	MP:0002875	decreased erythrocyte cell number	Rnf168<tm2b(EUCOMM)Hmgu>/Rnf168<tm2b(EUCOMM)Hmgu>	C57BL/6N-Rnf168<tm2b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6696882	F	MP:0002874	decreased hemoglobin content	Rnf168<tm2b(EUCOMM)Hmgu>/Rnf168<tm2b(EUCOMM)Hmgu>	C57BL/6N-Rnf168<tm2b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6696882	M	MP:0001566	increased circulating phosphate level	Rnf168<tm2b(EUCOMM)Hmgu>/Rnf168<tm2b(EUCOMM)Hmgu>	C57BL/6N-Rnf168<tm2b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6696882	M	MP:0000274	enlarged heart	Rnf168<tm2b(EUCOMM)Hmgu>/Rnf168<tm2b(EUCOMM)Hmgu>	C57BL/6N-Rnf168<tm2b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6696882	F	MP:0000689	abnormal spleen morphology	Rnf168<tm2b(EUCOMM)Hmgu>/Rnf168<tm2b(EUCOMM)Hmgu>	C57BL/6N-Rnf168<tm2b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6696882	M	MP:0001307	fused cornea and lens	Rnf168<tm2b(EUCOMM)Hmgu>/Rnf168<tm2b(EUCOMM)Hmgu>	C57BL/6N-Rnf168<tm2b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6696884	M	MP:0010024	increased total body fat amount	Rsu1<em1(IMPC)J>/Rsu1<+>	C57BL/6NJ-Rsu1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696885	M	MP:0000063	decreased bone mineral density	Rwdd2a<em1(IMPC)J>/Rwdd2a<em1(IMPC)J>	C57BL/6NJ-Rwdd2a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696885	M	MP:0000195	decreased circulating calcium level	Rwdd2a<em1(IMPC)J>/Rwdd2a<em1(IMPC)J>	C57BL/6NJ-Rwdd2a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696885	F	MP:0005343	increased circulating aspartate transaminase level	Rwdd2a<em1(IMPC)J>/Rwdd2a<em1(IMPC)J>	C57BL/6NJ-Rwdd2a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696885	M	MP:0010124	decreased bone mineral content	Rwdd2a<em1(IMPC)J>/Rwdd2a<em1(IMPC)J>	C57BL/6NJ-Rwdd2a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696885	M	MP:0000221	decreased leukocyte cell number	Rwdd2a<em1(IMPC)J>/Rwdd2a<em1(IMPC)J>	C57BL/6NJ-Rwdd2a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696885	M	MP:0003961	decreased lean body mass	Rwdd2a<em1(IMPC)J>/Rwdd2a<em1(IMPC)J>	C57BL/6NJ-Rwdd2a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696886	F	MP:0002941	increased circulating alanine transaminase level	Saa3<tm1.1(KOMP)Vlcg>/Saa3<tm1.1(KOMP)Vlcg>	C57BL/6N-Saa3<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6696886	F	MP:0011110	preweaning lethality, incomplete penetrance	Saa3<tm1.1(KOMP)Vlcg>/Saa3<tm1.1(KOMP)Vlcg>	C57BL/6N-Saa3<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6696887	M	MP:0005627	increased circulating potassium level	Sbsn<em1(IMPC)Ccpcz>/Sbsn<em1(IMPC)Ccpcz>	C57BL/6N-Sbsn<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696887	F	MP:0010090	increased circulating creatine kinase level	Sbsn<em1(IMPC)Ccpcz>/Sbsn<em1(IMPC)Ccpcz>	C57BL/6N-Sbsn<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696887	M	MP:0000266	abnormal heart morphology	Sbsn<em1(IMPC)Ccpcz>/Sbsn<em1(IMPC)Ccpcz>	C57BL/6N-Sbsn<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696887	M	MP:0008725	increased heart atrium size	Sbsn<em1(IMPC)Ccpcz>/Sbsn<em1(IMPC)Ccpcz>	C57BL/6N-Sbsn<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696887	F	MP:0002932	abnormal joint morphology	Sbsn<em1(IMPC)Ccpcz>/Sbsn<em1(IMPC)Ccpcz>	C57BL/6N-Sbsn<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696887	M	MP:0005634	decreased circulating sodium level	Sbsn<em1(IMPC)Ccpcz>/Sbsn<em1(IMPC)Ccpcz>	C57BL/6N-Sbsn<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696888	F	MP:0005562	decreased mean corpuscular hemoglobin	Scfd1<em1(IMPC)Tcp>/Scfd1<+>	C57BL/6N-Scfd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696888	F	MP:0002060	abnormal skin morphology	Scfd1<em1(IMPC)Tcp>/Scfd1<+>	C57BL/6N-Scfd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696891	M	MP:0000198	decreased circulating phosphate level	Sec31b<em1(IMPC)J>/Sec31b<em1(IMPC)J>	C57BL/6NJ-Sec31b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696892	M	MP:0000556	abnormal hindlimb morphology	Secisbp2l<em1(IMPC)J>/Secisbp2l<em1(IMPC)J>	C57BL/6NJ-Secisbp2l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696892	F	MP:0005178	increased circulating cholesterol level	Secisbp2l<em1(IMPC)J>/Secisbp2l<em1(IMPC)J>	C57BL/6NJ-Secisbp2l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696892	M	MP:0001488	increased startle reflex	Secisbp2l<em1(IMPC)J>/Secisbp2l<em1(IMPC)J>	C57BL/6NJ-Secisbp2l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696892	M	MP:0010052	increased grip strength	Secisbp2l<em1(IMPC)J>/Secisbp2l<em1(IMPC)J>	C57BL/6NJ-Secisbp2l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696892	F	MP:0005655	increased aggression	Secisbp2l<em1(IMPC)J>/Secisbp2l<em1(IMPC)J>	C57BL/6NJ-Secisbp2l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696892	M	MP:0005632	decreased circulating aspartate transaminase level	Secisbp2l<em1(IMPC)J>/Secisbp2l<em1(IMPC)J>	C57BL/6NJ-Secisbp2l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696893	M	MP:0000274	enlarged heart	Sema6c<em1(IMPC)Mbp>/Sema6c<em1(IMPC)Mbp>	C57BL/6N-Sema6c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696893	F	MP:0000601	small liver	Sema6c<em1(IMPC)Mbp>/Sema6c<em1(IMPC)Mbp>	C57BL/6N-Sema6c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696893	M	MP:0009476	enlarged cecum	Sema6c<em1(IMPC)Mbp>/Sema6c<em1(IMPC)Mbp>	C57BL/6N-Sema6c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696893	F	MP:0000598	abnormal liver morphology	Sema6c<em1(IMPC)Mbp>/Sema6c<em1(IMPC)Mbp>	C57BL/6N-Sema6c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696893	M	MP:0000494	abnormal cecum morphology	Sema6c<em1(IMPC)Mbp>/Sema6c<em1(IMPC)Mbp>	C57BL/6N-Sema6c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696893	M	MP:0005084	abnormal gallbladder morphology	Sema6c<em1(IMPC)Mbp>/Sema6c<em1(IMPC)Mbp>	C57BL/6N-Sema6c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696893	M	MP:0000266	abnormal heart morphology	Sema6c<em1(IMPC)Mbp>/Sema6c<em1(IMPC)Mbp>	C57BL/6N-Sema6c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696894	M	MP:0005562	decreased mean corpuscular hemoglobin	Sepsecs<em1(IMPC)Tcp>/Sepsecs<+>	C57BL/6N-Sepsecs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696894	F	MP:0000194	increased circulating calcium level	Sepsecs<em1(IMPC)Tcp>/Sepsecs<+>	C57BL/6N-Sepsecs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696894	M	MP:0001200	thick skin	Sepsecs<em1(IMPC)Tcp>/Sepsecs<+>	C57BL/6N-Sepsecs<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696895	M	MP:0002152	abnormal brain morphology	Serping1<em1(IMPC)Mbp>/Serping1<em1(IMPC)Mbp>	C57BL/6N-Serping1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696895	F	MP:0002966	decreased circulating alkaline phosphatase level	Serping1<em1(IMPC)Mbp>/Serping1<em1(IMPC)Mbp>	C57BL/6N-Serping1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696895	M	MP:0001304	cataract	Serping1<em1(IMPC)Mbp>/Serping1<em1(IMPC)Mbp>	C57BL/6N-Serping1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696895	M	MP:0000774	decreased brain size	Serping1<em1(IMPC)Mbp>/Serping1<em1(IMPC)Mbp>	C57BL/6N-Serping1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696896	F	MP:0001120	abnormal uterus morphology	Sgtb<em1(IMPC)Mbp>/Sgtb<em1(IMPC)Mbp>	C57BL/6NCrl-Sgtb<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6696897	F	MP:0002941	increased circulating alanine transaminase level	Sirpb1a<em1(IMPC)Wtsi>/Sirpb1a<em1(IMPC)Wtsi>	C57BL/6N-Sirpb1a<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696898	M	MP:0002644	decreased circulating triglyceride level	Slain2<em1(IMPC)J>/Slain2<+>	C57BL/6NJ-Slain2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696898	M	MP:0005179	decreased circulating cholesterol level	Slain2<em1(IMPC)J>/Slain2<+>	C57BL/6NJ-Slain2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696898	M	MP:0001399	hyperactivity	Slain2<em1(IMPC)J>/Slain2<+>	C57BL/6NJ-Slain2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696898	M	MP:0000367	abnormal coat/ hair morphology	Slain2<em1(IMPC)J>/Slain2<+>	C57BL/6NJ-Slain2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696898	M	MP:0005635	decreased circulating bilirubin level	Slain2<em1(IMPC)J>/Slain2<+>	C57BL/6NJ-Slain2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696899	M	MP:0000266	abnormal heart morphology	Slc10a1<em1(IMPC)Mbp>/Slc10a1<em1(IMPC)Mbp>	C57BL/6N-Slc10a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696899	M	MP:0002059	abnormal seminal vesicle morphology	Slc10a1<em1(IMPC)Mbp>/Slc10a1<em1(IMPC)Mbp>	C57BL/6N-Slc10a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696899	M	MP:0000274	enlarged heart	Slc10a1<em1(IMPC)Mbp>/Slc10a1<em1(IMPC)Mbp>	C57BL/6N-Slc10a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696899	M	MP:0002699	abnormal vitreous body morphology	Slc10a1<em1(IMPC)Mbp>/Slc10a1<em1(IMPC)Mbp>	C57BL/6N-Slc10a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696899	M	MP:0001157	small seminal vesicle	Slc10a1<em1(IMPC)Mbp>/Slc10a1<em1(IMPC)Mbp>	C57BL/6N-Slc10a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696899	M	MP:0001304	cataract	Slc10a1<em1(IMPC)Mbp>/Slc10a1<em1(IMPC)Mbp>	C57BL/6N-Slc10a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696899	F	MP:0002060	abnormal skin morphology	Slc10a1<em1(IMPC)Mbp>/Slc10a1<em1(IMPC)Mbp>	C57BL/6N-Slc10a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696899	M	MP:0000598	abnormal liver morphology	Slc10a1<em1(IMPC)Mbp>/Slc10a1<em1(IMPC)Mbp>	C57BL/6N-Slc10a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696900	M	MP:0005178	increased circulating cholesterol level	Slc10a3<em1(IMPC)J>/Y	C57BL/6NJ-Slc10a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696900	M	MP:0010124	decreased bone mineral content	Slc10a3<em1(IMPC)J>/Y	C57BL/6NJ-Slc10a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696900	M	MP:0001556	increased circulating HDL cholesterol level	Slc10a3<em1(IMPC)J>/Y	C57BL/6NJ-Slc10a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696903	M	MP:0003642	absent seminal vesicle	Slc25a18<tm1b(KOMP)Wtsi>/Slc25a18<tm1b(KOMP)Wtsi>	C57BL/6N-Slc25a18<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6696903	F	MP:0010052	increased grip strength	Slc25a18<tm1b(KOMP)Wtsi>/Slc25a18<tm1b(KOMP)Wtsi>	C57BL/6N-Slc25a18<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6696903	F	MP:0009454	impaired contextual conditioning behavior	Slc25a18<tm1b(KOMP)Wtsi>/Slc25a18<tm1b(KOMP)Wtsi>	C57BL/6N-Slc25a18<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6696903	M	MP:0002059	abnormal seminal vesicle morphology	Slc25a18<tm1b(KOMP)Wtsi>/Slc25a18<tm1b(KOMP)Wtsi>	C57BL/6N-Slc25a18<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6696903	M	MP:0002941	increased circulating alanine transaminase level	Slc25a18<tm1b(KOMP)Wtsi>/Slc25a18<tm1b(KOMP)Wtsi>	C57BL/6N-Slc25a18<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6696903	M	MP:0005293	impaired glucose tolerance	Slc25a18<tm1b(KOMP)Wtsi>/Slc25a18<tm1b(KOMP)Wtsi>	C57BL/6N-Slc25a18<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6696904	F	MP:0000221	decreased leukocyte cell number	Slc25a42<em1(IMPC)J>/Slc25a42<+>	C57BL/6NJ-Slc25a42<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696905	F	MP:0001399	hyperactivity	Slc25a44<em1(IMPC)J>/Slc25a44<em1(IMPC)J>	C57BL/6NJ-Slc25a44<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696906	F	MP:0005567	decreased circulating total protein level	Slc29a3<em1(IMPC)Wtsi>/Slc29a3<em1(IMPC)Wtsi>	C57BL/6N-Slc29a3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696906	F	MP:0005419	decreased circulating serum albumin level	Slc29a3<em1(IMPC)Wtsi>/Slc29a3<em1(IMPC)Wtsi>	C57BL/6N-Slc29a3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696906	F	MP:0005344	increased circulating bilirubin level	Slc29a3<em1(IMPC)Wtsi>/Slc29a3<em1(IMPC)Wtsi>	C57BL/6N-Slc29a3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696906	F	MP:0002941	increased circulating alanine transaminase level	Slc29a3<em1(IMPC)Wtsi>/Slc29a3<em1(IMPC)Wtsi>	C57BL/6N-Slc29a3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696906	F	MP:0005633	increased circulating sodium level	Slc29a3<em1(IMPC)Wtsi>/Slc29a3<em1(IMPC)Wtsi>	C57BL/6N-Slc29a3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696906	F	MP:0000218	increased leukocyte cell number	Slc29a3<em1(IMPC)Wtsi>/Slc29a3<em1(IMPC)Wtsi>	C57BL/6N-Slc29a3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696906	M	MP:0005560	decreased circulating glucose level	Slc29a3<em1(IMPC)Wtsi>/Slc29a3<em1(IMPC)Wtsi>	C57BL/6N-Slc29a3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696906	M	MP:0005562	decreased mean corpuscular hemoglobin	Slc29a3<em1(IMPC)Wtsi>/Slc29a3<em1(IMPC)Wtsi>	C57BL/6N-Slc29a3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696906	M	MP:0002644	decreased circulating triglyceride level	Slc29a3<em1(IMPC)Wtsi>/Slc29a3<em1(IMPC)Wtsi>	C57BL/6N-Slc29a3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696906	F	MP:0005343	increased circulating aspartate transaminase level	Slc29a3<em1(IMPC)Wtsi>/Slc29a3<em1(IMPC)Wtsi>	C57BL/6N-Slc29a3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696907	M	MP:0002075	abnormal coat/hair pigmentation	Slc41a2<em1(IMPC)J>/Slc41a2<em1(IMPC)J>	C57BL/6NJ-Slc41a2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696907	M	MP:0001529	abnormal vocalization	Slc41a2<em1(IMPC)J>/Slc41a2<em1(IMPC)J>	C57BL/6NJ-Slc41a2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696908	M	MP:0009476	enlarged cecum	Slc49a4<em1(IMPC)Mbp>/Slc49a4<em1(IMPC)Mbp>	C57BL/6N-Slc49a4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696908	M	MP:0000494	abnormal cecum morphology	Slc49a4<em1(IMPC)Mbp>/Slc49a4<em1(IMPC)Mbp>	C57BL/6N-Slc49a4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696909	M	MP:0005343	increased circulating aspartate transaminase level	Smarca2<em1(IMPC)J>/Smarca2<em1(IMPC)J>	C57BL/6NJ-Smarca2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696909	M	MP:0005344	increased circulating bilirubin level	Smarca2<em1(IMPC)J>/Smarca2<em1(IMPC)J>	C57BL/6NJ-Smarca2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696909	F	MP:0001399	hyperactivity	Smarca2<em1(IMPC)J>/Smarca2<em1(IMPC)J>	C57BL/6NJ-Smarca2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696910	M	MP:0002590	increased mean corpuscular volume	Smarcc2<em1(IMPC)J>/Smarcc2<+>	C57BL/6NJ-Smarcc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696910	M	MP:0010506	prolonged RR interval	Smarcc2<em1(IMPC)J>/Smarcc2<+>	C57BL/6NJ-Smarcc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696910	M	MP:0005333	decreased heart rate	Smarcc2<em1(IMPC)J>/Smarcc2<+>	C57BL/6NJ-Smarcc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696914	M	MP:0002591	decreased mean corpuscular volume	Snx13<tm1b(EUCOMM)Hmgu>/Snx13<+>	C57BL/6N-Snx13<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6696914	M	MP:0000218	increased leukocyte cell number	Snx13<tm1b(EUCOMM)Hmgu>/Snx13<+>	C57BL/6N-Snx13<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6696916	F	MP:0001399	hyperactivity	Specc1l<em1(IMPC)J>/Specc1l<em1(IMPC)J>	C57BL/6NJ-Specc1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696916	M	MP:0000195	decreased circulating calcium level	Specc1l<em1(IMPC)J>/Specc1l<em1(IMPC)J>	C57BL/6NJ-Specc1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696917	F	MP:0009142	decreased prepulse inhibition	Ssc4d<em1(IMPC)J>/Ssc4d<em1(IMPC)J>	C57BL/6NJ-Ssc4d<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696918	F	MP:0000598	abnormal liver morphology	Ssr1<em1(IMPC)Mbp>/Ssr1<+>	C57BL/6N-Ssr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696918	M	MP:0000691	enlarged spleen	Ssr1<em1(IMPC)Mbp>/Ssr1<+>	C57BL/6N-Ssr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696918	F	MP:0002135	abnormal kidney morphology	Ssr1<em1(IMPC)Mbp>/Ssr1<+>	C57BL/6N-Ssr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696918	M	MP:0001148	enlarged testis	Ssr1<em1(IMPC)Mbp>/Ssr1<+>	C57BL/6N-Ssr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696918	F	MP:0002989	small kidney	Ssr1<em1(IMPC)Mbp>/Ssr1<+>	C57BL/6N-Ssr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696918	F	MP:0002060	abnormal skin morphology	Ssr1<em1(IMPC)Mbp>/Ssr1<+>	C57BL/6N-Ssr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696918	F	MP:0000601	small liver	Ssr1<em1(IMPC)Mbp>/Ssr1<+>	C57BL/6N-Ssr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696918	M	MP:0001146	abnormal testis morphology	Ssr1<em1(IMPC)Mbp>/Ssr1<+>	C57BL/6N-Ssr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696918	F	MP:0001289	persistence of hyaloid vascular system	Ssr1<em1(IMPC)Mbp>/Ssr1<+>	C57BL/6N-Ssr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696918	M	MP:0000689	abnormal spleen morphology	Ssr1<em1(IMPC)Mbp>/Ssr1<+>	C57BL/6N-Ssr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696919	F	MP:0000691	enlarged spleen	St8sia6<em1(IMPC)Mbp>/St8sia6<em1(IMPC)Mbp>	C57BL/6N-St8sia6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696919	F	MP:0000689	abnormal spleen morphology	St8sia6<em1(IMPC)Mbp>/St8sia6<em1(IMPC)Mbp>	C57BL/6N-St8sia6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696919	F	MP:0002699	abnormal vitreous body morphology	St8sia6<em1(IMPC)Mbp>/St8sia6<em1(IMPC)Mbp>	C57BL/6N-St8sia6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696920	M	MP:0005419	decreased circulating serum albumin level	Stard7<tm1b(EUCOMM)Wtsi>/Stard7<+>	C57BL/6N-Stard7<tm1b(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696922	M	MP:0002135	abnormal kidney morphology	Stat4<em1(IMPC)Mbp>/Stat4<em1(IMPC)Mbp>	C57BL/6N-Stat4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696922	M	MP:0002699	abnormal vitreous body morphology	Stat4<em1(IMPC)Mbp>/Stat4<em1(IMPC)Mbp>	C57BL/6N-Stat4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696922	M	MP:0001304	cataract	Stat4<em1(IMPC)Mbp>/Stat4<em1(IMPC)Mbp>	C57BL/6N-Stat4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696922	M	MP:0001314	cornea opacity	Stat4<em1(IMPC)Mbp>/Stat4<em1(IMPC)Mbp>	C57BL/6N-Stat4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696922	M	MP:0002989	small kidney	Stat4<em1(IMPC)Mbp>/Stat4<em1(IMPC)Mbp>	C57BL/6N-Stat4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696925	M	MP:0008805	decreased circulating amylase level	Strbp<em1(IMPC)Hmgu>/Strbp<em1(IMPC)Hmgu>	C57BL/6N-Strbp<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696925	M	MP:0001489	decreased startle reflex	Strbp<em1(IMPC)Hmgu>/Strbp<em1(IMPC)Hmgu>	C57BL/6N-Strbp<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696925	M	MP:0001392	abnormal locomotor behavior	Strbp<em1(IMPC)Hmgu>/Strbp<em1(IMPC)Hmgu>	C57BL/6N-Strbp<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696925	F	MP:0001364	decreased anxiety-related response	Strbp<em1(IMPC)Hmgu>/Strbp<em1(IMPC)Hmgu>	C57BL/6N-Strbp<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696925	F	MP:0001486	abnormal startle reflex	Strbp<em1(IMPC)Hmgu>/Strbp<em1(IMPC)Hmgu>	C57BL/6N-Strbp<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696925	M	MP:0001512	trunk curl	Strbp<em1(IMPC)Hmgu>/Strbp<em1(IMPC)Hmgu>	C57BL/6N-Strbp<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696926	M	MP:0001147	small testis	Sycp2<tm1b(EUCOMM)Hmgu>/Sycp2<tm1b(EUCOMM)Hmgu>	C57BL/6N-Sycp2<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6696927	F	MP:0002968	increased circulating alkaline phosphatase level	Syncrip<tm1b(EUCOMM)Hmgu>/Syncrip<+>	C57BL/6N-Syncrip<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6696927	M	MP:0010123	increased bone mineral content	Syncrip<tm1b(EUCOMM)Hmgu>/Syncrip<+>	C57BL/6N-Syncrip<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6696927	F	MP:0010052	increased grip strength	Syncrip<tm1b(EUCOMM)Hmgu>/Syncrip<+>	C57BL/6N-Syncrip<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6696928	F	MP:0005292	improved glucose tolerance	Sytl4<em1(IMPC)Hmgu>/Sytl4<em1(IMPC)Hmgu>	C57BL/6N-Sytl4<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696928	F	MP:0001489	decreased startle reflex	Sytl4<em1(IMPC)Hmgu>/Sytl4<em1(IMPC)Hmgu>	C57BL/6N-Sytl4<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696929	F	MP:0002989	small kidney	Taar3<em1(IMPC)Mbp>/Taar3<em1(IMPC)Mbp>	C57BL/6N-Taar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696929	M	MP:0002152	abnormal brain morphology	Taar3<em1(IMPC)Mbp>/Taar3<em1(IMPC)Mbp>	C57BL/6N-Taar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696929	M	MP:0000774	decreased brain size	Taar3<em1(IMPC)Mbp>/Taar3<em1(IMPC)Mbp>	C57BL/6N-Taar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696929	F	MP:0002135	abnormal kidney morphology	Taar3<em1(IMPC)Mbp>/Taar3<em1(IMPC)Mbp>	C57BL/6N-Taar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696930	F	MP:0000689	abnormal spleen morphology	Taar8b<em1(IMPC)Mbp>/Taar8b<em1(IMPC)Mbp>	C57BL/6N-Taar8b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696930	F	MP:0000601	small liver	Taar8b<em1(IMPC)Mbp>/Taar8b<em1(IMPC)Mbp>	C57BL/6N-Taar8b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696930	F	MP:0000598	abnormal liver morphology	Taar8b<em1(IMPC)Mbp>/Taar8b<em1(IMPC)Mbp>	C57BL/6N-Taar8b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696930	M	MP:0001304	cataract	Taar8b<em1(IMPC)Mbp>/Taar8b<em1(IMPC)Mbp>	C57BL/6N-Taar8b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696930	F	MP:0020421	increased freezing behavior	Taar8b<em1(IMPC)Mbp>/Taar8b<em1(IMPC)Mbp>	C57BL/6N-Taar8b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696930	F	MP:0000759	abnormal skeletal muscle morphology	Taar8b<em1(IMPC)Mbp>/Taar8b<em1(IMPC)Mbp>	C57BL/6N-Taar8b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696930	M	MP:0002699	abnormal vitreous body morphology	Taar8b<em1(IMPC)Mbp>/Taar8b<em1(IMPC)Mbp>	C57BL/6N-Taar8b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696930	M	MP:0001402	decreased locomotor activity	Taar8b<em1(IMPC)Mbp>/Taar8b<em1(IMPC)Mbp>	C57BL/6N-Taar8b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696930	F	MP:0000691	enlarged spleen	Taar8b<em1(IMPC)Mbp>/Taar8b<em1(IMPC)Mbp>	C57BL/6N-Taar8b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696932	F	MP:0000063	decreased bone mineral density	Tacr3<em1(IMPC)J>/Tacr3<em1(IMPC)J>	C57BL/6NJ-Tacr3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696932	F	MP:0010124	decreased bone mineral content	Tacr3<em1(IMPC)J>/Tacr3<em1(IMPC)J>	C57BL/6NJ-Tacr3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696932	F	MP:0001926	female infertility	Tacr3<em1(IMPC)J>/Tacr3<em1(IMPC)J>	C57BL/6NJ-Tacr3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696932	F	MP:0010024	increased total body fat amount	Tacr3<em1(IMPC)J>/Tacr3<em1(IMPC)J>	C57BL/6NJ-Tacr3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696933	M	MP:0001925	male infertility	Tbc1d21<em1(IMPC)J>/Tbc1d21<em1(IMPC)J>	C57BL/6NJ-Tbc1d21<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696934	M	MP:0005178	increased circulating cholesterol level	Tbc1d9b<em1(IMPC)J>/Tbc1d9b<em1(IMPC)J>	C57BL/6NJ-Tbc1d9b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696934	M	MP:0001556	increased circulating HDL cholesterol level	Tbc1d9b<em1(IMPC)J>/Tbc1d9b<em1(IMPC)J>	C57BL/6NJ-Tbc1d9b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696936	M	MP:0000269	abnormal heart looping	Tgds<em1(IMPC)Mbp>/Tgds<em1(IMPC)Mbp>	C57BL/6N-Tgds<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696936	F	MP:0003425	abnormal optic vesicle formation	Tgds<em1(IMPC)Mbp>/Tgds<em1(IMPC)Mbp>	C57BL/6N-Tgds<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696938	M	MP:0003393	decreased cardiac output	Thyn1<em1(IMPC)Bay>/Thyn1<em1(IMPC)Bay>	C57BL/6N-Thyn1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6696940	F	MP:0010052	increased grip strength	Tldc2<em1(IMPC)J>/Tldc2<em1(IMPC)J>	C57BL/6NJ-Tldc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696942	M	MP:0000702	enlarged lymph nodes	Tm9sf2<em1(IMPC)Tcp>/Tm9sf2<+>	C57BL/6N-Tm9sf2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696942	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Tm9sf2<em1(IMPC)Tcp>/Tm9sf2<+>	C57BL/6N-Tm9sf2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696943	M	MP:0003231	abnormal placenta vasculature	Tmcc2<em1(IMPC)Mbp>/Tmcc2<em1(IMPC)Mbp>	C57BL/6N-Tmcc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696944	M	MP:0002079	increased circulating insulin level	Tmem163<em1(IMPC)Mbp>/Tmem163<em1(IMPC)Mbp>	C57BL/6N-Tmem163<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696944	M	MP:0002060	abnormal skin morphology	Tmem163<em1(IMPC)Mbp>/Tmem163<em1(IMPC)Mbp>	C57BL/6N-Tmem163<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696944	F	MP:0006203	eye hemorrhage	Tmem163<em1(IMPC)Mbp>/Tmem163<em1(IMPC)Mbp>	C57BL/6N-Tmem163<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696945	F	MP:0000689	abnormal spleen morphology	Tmem88b<em1(IMPC)Mbp>/Tmem88b<em1(IMPC)Mbp>	C57BL/6N-Tmem88b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696945	M	MP:0001146	abnormal testis morphology	Tmem88b<em1(IMPC)Mbp>/Tmem88b<em1(IMPC)Mbp>	C57BL/6N-Tmem88b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696945	M	MP:0001147	small testis	Tmem88b<em1(IMPC)Mbp>/Tmem88b<em1(IMPC)Mbp>	C57BL/6N-Tmem88b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696945	F	MP:0002060	abnormal skin morphology	Tmem88b<em1(IMPC)Mbp>/Tmem88b<em1(IMPC)Mbp>	C57BL/6N-Tmem88b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696946	F	MP:0002989	small kidney	Tnfsf8<em1(IMPC)Mbp>/Tnfsf8<em1(IMPC)Mbp>	C57BL/6N-Tnfsf8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696946	F	MP:0002060	abnormal skin morphology	Tnfsf8<em1(IMPC)Mbp>/Tnfsf8<em1(IMPC)Mbp>	C57BL/6N-Tnfsf8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696946	M	MP:0001146	abnormal testis morphology	Tnfsf8<em1(IMPC)Mbp>/Tnfsf8<em1(IMPC)Mbp>	C57BL/6N-Tnfsf8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696946	F	MP:0002135	abnormal kidney morphology	Tnfsf8<em1(IMPC)Mbp>/Tnfsf8<em1(IMPC)Mbp>	C57BL/6N-Tnfsf8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696946	M	MP:0001148	enlarged testis	Tnfsf8<em1(IMPC)Mbp>/Tnfsf8<em1(IMPC)Mbp>	C57BL/6N-Tnfsf8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696948	F	MP:0001297	microphthalmia	Tprg1<em1(IMPC)Mbp>/Tprg1<em1(IMPC)Mbp>	C57BL/6N-Tprg1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696948	F	MP:0005084	abnormal gallbladder morphology	Tprg1<em1(IMPC)Mbp>/Tprg1<em1(IMPC)Mbp>	C57BL/6N-Tprg1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696948	M	MP:0011110	preweaning lethality, incomplete penetrance	Tprg1<em1(IMPC)Mbp>/Tprg1<em1(IMPC)Mbp>	C57BL/6N-Tprg1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696948	F	MP:0009342	enlarged gallbladder	Tprg1<em1(IMPC)Mbp>/Tprg1<em1(IMPC)Mbp>	C57BL/6N-Tprg1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696948	F	MP:0002092	abnormal eye morphology	Tprg1<em1(IMPC)Mbp>/Tprg1<em1(IMPC)Mbp>	C57BL/6N-Tprg1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696949	F	MP:0005553	increased circulating creatinine level	Trappc11<em1(IMPC)J>/Trappc11<+>	C57BL/6NJ-Trappc11<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696951	M	MP:0010024	increased total body fat amount	Trim35<em1(IMPC)J>/Trim35<em1(IMPC)J>	C57BL/6NJ-Trim35<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696952	M	MP:0001146	abnormal testis morphology	Trp53inp2<em1(IMPC)Mbp>/Trp53inp2<em1(IMPC)Mbp>	C57BL/6N-Trp53inp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696952	F	MP:0002092	abnormal eye morphology	Trp53inp2<em1(IMPC)Mbp>/Trp53inp2<em1(IMPC)Mbp>	C57BL/6N-Trp53inp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696952	F	MP:0002060	abnormal skin morphology	Trp53inp2<em1(IMPC)Mbp>/Trp53inp2<em1(IMPC)Mbp>	C57BL/6N-Trp53inp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696952	M	MP:0000598	abnormal liver morphology	Trp53inp2<em1(IMPC)Mbp>/Trp53inp2<em1(IMPC)Mbp>	C57BL/6N-Trp53inp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696952	M	MP:0000599	enlarged liver	Trp53inp2<em1(IMPC)Mbp>/Trp53inp2<em1(IMPC)Mbp>	C57BL/6N-Trp53inp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696952	M	MP:0000702	enlarged lymph nodes	Trp53inp2<em1(IMPC)Mbp>/Trp53inp2<em1(IMPC)Mbp>	C57BL/6N-Trp53inp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696952	M	MP:0009142	decreased prepulse inhibition	Trp53inp2<em1(IMPC)Mbp>/Trp53inp2<em1(IMPC)Mbp>	C57BL/6N-Trp53inp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696952	M	MP:0001148	enlarged testis	Trp53inp2<em1(IMPC)Mbp>/Trp53inp2<em1(IMPC)Mbp>	C57BL/6N-Trp53inp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696952	M	MP:0002339	abnormal lymph node morphology	Trp53inp2<em1(IMPC)Mbp>/Trp53inp2<em1(IMPC)Mbp>	C57BL/6N-Trp53inp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696953	M	MP:0005333	decreased heart rate	Try10<em1(IMPC)J>/Try10<em1(IMPC)J>	C57BL/6NJ-Try10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696953	F	MP:0005553	increased circulating creatinine level	Try10<em1(IMPC)J>/Try10<em1(IMPC)J>	C57BL/6NJ-Try10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696953	F	MP:0000221	decreased leukocyte cell number	Try10<em1(IMPC)J>/Try10<em1(IMPC)J>	C57BL/6NJ-Try10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696953	M	MP:0010506	prolonged RR interval	Try10<em1(IMPC)J>/Try10<em1(IMPC)J>	C57BL/6NJ-Try10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696953	M	MP:0020870	decreased thigmotaxis	Try10<em1(IMPC)J>/Try10<em1(IMPC)J>	C57BL/6NJ-Try10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696954	M	MP:0001146	abnormal testis morphology	Tspan32<em1(IMPC)Mbp>/Tspan32<em1(IMPC)Mbp>	C57BL/6N-Tspan32<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696954	M	MP:0001200	thick skin	Tspan32<em1(IMPC)Mbp>/Tspan32<em1(IMPC)Mbp>	C57BL/6N-Tspan32<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696954	F	MP:0000598	abnormal liver morphology	Tspan32<em1(IMPC)Mbp>/Tspan32<em1(IMPC)Mbp>	C57BL/6N-Tspan32<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696954	M	MP:0003883	enlarged stomach	Tspan32<em1(IMPC)Mbp>/Tspan32<em1(IMPC)Mbp>	C57BL/6N-Tspan32<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696954	M	MP:0001147	small testis	Tspan32<em1(IMPC)Mbp>/Tspan32<em1(IMPC)Mbp>	C57BL/6N-Tspan32<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696954	M	MP:0002997	enlarged seminal vesicle	Tspan32<em1(IMPC)Mbp>/Tspan32<em1(IMPC)Mbp>	C57BL/6N-Tspan32<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696954	M	MP:0002060	abnormal skin morphology	Tspan32<em1(IMPC)Mbp>/Tspan32<em1(IMPC)Mbp>	C57BL/6N-Tspan32<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696954	F	MP:0002092	abnormal eye morphology	Tspan32<em1(IMPC)Mbp>/Tspan32<em1(IMPC)Mbp>	C57BL/6N-Tspan32<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696954	M	MP:0000470	abnormal stomach morphology	Tspan32<em1(IMPC)Mbp>/Tspan32<em1(IMPC)Mbp>	C57BL/6N-Tspan32<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696955	M	MP:0009552	urinary bladder obstruction	Ttc1<em1(IMPC)Mbp>/Ttc1<+>	C57BL/6N-Ttc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696956	M	MP:0010393	shortened QRS complex duration	Ttc29<em1(IMPC)J>/Ttc29<em1(IMPC)J>	C57BL/6NJ-Ttc29<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696957	M	MP:0001399	hyperactivity	Tubal3<em1(IMPC)J>/Tubal3<em1(IMPC)J>	C57BL/6NJ-Tubal3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696957	M	MP:0000221	decreased leukocyte cell number	Tubal3<em1(IMPC)J>/Tubal3<em1(IMPC)J>	C57BL/6NJ-Tubal3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696957	M	MP:0000195	decreased circulating calcium level	Tubal3<em1(IMPC)J>/Tubal3<em1(IMPC)J>	C57BL/6NJ-Tubal3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696957	M	MP:0002574	increased vertical activity	Tubal3<em1(IMPC)J>/Tubal3<em1(IMPC)J>	C57BL/6NJ-Tubal3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696958	F	MP:0013278	decreased fasting circulating glucose level	Tubb4a<tm1.1(KOMP)Wtsi>/Tubb4a<tm1.1(KOMP)Wtsi>	C57BL/6N-Tubb4a<tm1.1(KOMP)Wtsi>/J	N	MGI:5576271
MGI:6696959	M	MP:0000157	abnormal sternum morphology	Tubgcp2<em1(IMPC)Tcp>/Tubgcp2<+>	C57BL/6N-Tubgcp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696961	M	MP:0001304	cataract	Tulp2<em1(IMPC)Mbp>/Tulp2<em1(IMPC)Mbp>	C57BL/6N-Tulp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696961	M	MP:0001925	male infertility	Tulp2<em1(IMPC)Mbp>/Tulp2<em1(IMPC)Mbp>	C57BL/6N-Tulp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696961	M	MP:0002699	abnormal vitreous body morphology	Tulp2<em1(IMPC)Mbp>/Tulp2<em1(IMPC)Mbp>	C57BL/6N-Tulp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696962	M	MP:0000702	enlarged lymph nodes	Ube4a<em1(IMPC)Tcp>/Ube4a<em1(IMPC)Tcp>	C57BL/6N-Ube4a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696962	F	MP:0003961	decreased lean body mass	Ube4a<em1(IMPC)Tcp>/Ube4a<em1(IMPC)Tcp>	C57BL/6N-Ube4a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696962	F	MP:0002764	short tibia	Ube4a<em1(IMPC)Tcp>/Ube4a<em1(IMPC)Tcp>	C57BL/6N-Ube4a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696962	F	MP:0010024	increased total body fat amount	Ube4a<em1(IMPC)Tcp>/Ube4a<em1(IMPC)Tcp>	C57BL/6N-Ube4a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696963	M	MP:0001417	decreased exploration in new environment	Ubn2<em1(IMPC)Tcp>/Ubn2<+>	C57BL/6N-Ubn2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696963	F	MP:0005562	decreased mean corpuscular hemoglobin	Ubn2<em1(IMPC)Tcp>/Ubn2<+>	C57BL/6N-Ubn2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6696964	F	MP:0000598	abnormal liver morphology	Uggt2<tm1b(KOMP)Wtsi>/Uggt2<tm1b(KOMP)Wtsi>	C57BL/6N-Uggt2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6696964	F	MP:0002581	abnormal ileum morphology	Uggt2<tm1b(KOMP)Wtsi>/Uggt2<tm1b(KOMP)Wtsi>	C57BL/6N-Uggt2<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:6696966	M	MP:0013279	increased fasting circulating glucose level	Uri1<tm1a(EUCOMM)Wtsi>/Uri1<tm1a(EUCOMM)Wtsi>	C57BL/6N-Uri1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696967	F	MP:0005343	increased circulating aspartate transaminase level	Urm1<em1(IMPC)J>/Urm1<+>	C57BL/6NJ-Urm1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696967	M	MP:0005178	increased circulating cholesterol level	Urm1<em1(IMPC)J>/Urm1<+>	C57BL/6NJ-Urm1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696969	M	MP:0003179	thrombocytopenia	Usp30<tm2b(EUCOMM)Hmgu>/Usp30<tm2b(EUCOMM)Hmgu>	C57BL/6N-Usp30<tm2b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6696969	M	MP:0002968	increased circulating alkaline phosphatase level	Usp30<tm2b(EUCOMM)Hmgu>/Usp30<tm2b(EUCOMM)Hmgu>	C57BL/6N-Usp30<tm2b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6696969	M	MP:0005293	impaired glucose tolerance	Usp30<tm2b(EUCOMM)Hmgu>/Usp30<tm2b(EUCOMM)Hmgu>	C57BL/6N-Usp30<tm2b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6696971	F	MP:0005553	increased circulating creatinine level	Wdr89<tm1a(KOMP)Wtsi>/Wdr89<tm1a(KOMP)Wtsi>	C57BL/6N-Wdr89<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6696972	M	MP:0002060	abnormal skin morphology	Xaf1<em1(IMPC)Mbp>/Xaf1<em1(IMPC)Mbp>	C57BL/6N-Xaf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696972	M	MP:0003883	enlarged stomach	Xaf1<em1(IMPC)Mbp>/Xaf1<em1(IMPC)Mbp>	C57BL/6N-Xaf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696972	M	MP:0000470	abnormal stomach morphology	Xaf1<em1(IMPC)Mbp>/Xaf1<em1(IMPC)Mbp>	C57BL/6N-Xaf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696973	F	MP:0001415	increased exploration in new environment	Ykt6<em1(IMPC)J>/Ykt6<+>	C57BL/6NJ-Ykt6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696973	F	MP:0000221	decreased leukocyte cell number	Ykt6<em1(IMPC)J>/Ykt6<+>	C57BL/6NJ-Ykt6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696974	F	MP:0001417	decreased exploration in new environment	Zbtb12<em1(IMPC)J>/Zbtb12<em1(IMPC)J>	C57BL/6NJ-Zbtb12<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696974	F	MP:0001402	decreased locomotor activity	Zbtb12<em1(IMPC)J>/Zbtb12<em1(IMPC)J>	C57BL/6NJ-Zbtb12<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696976	M	MP:0010393	shortened QRS complex duration	Zc3h7b<em1(IMPC)J>/Zc3h7b<em1(IMPC)J>	C57BL/6NJ-Zc3h7b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696977	M	MP:0000266	abnormal heart morphology	Zc3h8<em1(IMPC)Ccpcz>/Zc3h8<+>	C57BL/6N-Zc3h8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696977	M	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number	Zc3h8<em1(IMPC)Ccpcz>/Zc3h8<+>	C57BL/6N-Zc3h8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696977	M	MP:0000598	abnormal liver morphology	Zc3h8<em1(IMPC)Ccpcz>/Zc3h8<+>	C57BL/6N-Zc3h8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696977	F	MP:0002135	abnormal kidney morphology	Zc3h8<em1(IMPC)Ccpcz>/Zc3h8<+>	C57BL/6N-Zc3h8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696977	F	MP:0000689	abnormal spleen morphology	Zc3h8<em1(IMPC)Ccpcz>/Zc3h8<+>	C57BL/6N-Zc3h8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696977	F	MP:0003604	single kidney	Zc3h8<em1(IMPC)Ccpcz>/Zc3h8<+>	C57BL/6N-Zc3h8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696977	F	MP:0003068	enlarged kidney	Zc3h8<em1(IMPC)Ccpcz>/Zc3h8<+>	C57BL/6N-Zc3h8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696977	F	MP:0000691	enlarged spleen	Zc3h8<em1(IMPC)Ccpcz>/Zc3h8<+>	C57BL/6N-Zc3h8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696977	M	MP:0000274	enlarged heart	Zc3h8<em1(IMPC)Ccpcz>/Zc3h8<+>	C57BL/6N-Zc3h8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696977	M	MP:0000599	enlarged liver	Zc3h8<em1(IMPC)Ccpcz>/Zc3h8<+>	C57BL/6N-Zc3h8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696980	M	MP:0000221	decreased leukocyte cell number	Zfand3<em1(IMPC)J>/Zfand3<em1(IMPC)J>	C57BL/6NJ-Zfand3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696980	M	MP:0005567	decreased circulating total protein level	Zfand3<em1(IMPC)J>/Zfand3<em1(IMPC)J>	C57BL/6NJ-Zfand3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696980	M	MP:0003179	thrombocytopenia	Zfand3<em1(IMPC)J>/Zfand3<em1(IMPC)J>	C57BL/6NJ-Zfand3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696980	M	MP:0005560	decreased circulating glucose level	Zfand3<em1(IMPC)J>/Zfand3<em1(IMPC)J>	C57BL/6NJ-Zfand3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696980	M	MP:0000195	decreased circulating calcium level	Zfand3<em1(IMPC)J>/Zfand3<em1(IMPC)J>	C57BL/6NJ-Zfand3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696980	M	MP:0002574	increased vertical activity	Zfand3<em1(IMPC)J>/Zfand3<em1(IMPC)J>	C57BL/6NJ-Zfand3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696981	M	MP:0003984	embryonic growth retardation	Zfc3h1<em1(IMPC)Mbp>/Zfc3h1<em1(IMPC)Mbp>	C57BL/6N-Zfc3h1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6696982	F	MP:0009709	hydrometra	Zfp111<tm1b(KOMP)Wtsi>/Zfp111<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp111<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6696982	F	MP:0001120	abnormal uterus morphology	Zfp111<tm1b(KOMP)Wtsi>/Zfp111<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp111<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6696982	M	MP:0002060	abnormal skin morphology	Zfp111<tm1b(KOMP)Wtsi>/Zfp111<tm1b(KOMP)Wtsi>	C57BL/6N-Zfp111<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6696983	M	MP:0005505	thrombocytosis	Zfp219<tm1b(EUCOMM)Hmgu>/Zfp219<+>	C57BL/6N-Zfp219<tm1b(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6696984	M	MP:0001486	abnormal startle reflex	Zfp280d<em1(IMPC)Hmgu>/Zfp280d<em1(IMPC)Hmgu>	C57BL/6N-Zfp280d<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696984	M	MP:0005333	decreased heart rate	Zfp280d<em1(IMPC)Hmgu>/Zfp280d<em1(IMPC)Hmgu>	C57BL/6N-Zfp280d<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696984	M	MP:0010392	prolonged QRS complex duration	Zfp280d<em1(IMPC)Hmgu>/Zfp280d<em1(IMPC)Hmgu>	C57BL/6N-Zfp280d<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696984	M	MP:0002753	dilated heart left ventricle	Zfp280d<em1(IMPC)Hmgu>/Zfp280d<em1(IMPC)Hmgu>	C57BL/6N-Zfp280d<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696984	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Zfp280d<em1(IMPC)Hmgu>/Zfp280d<em1(IMPC)Hmgu>	C57BL/6N-Zfp280d<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696984	M	MP:0005140	decreased cardiac muscle contractility	Zfp280d<em1(IMPC)Hmgu>/Zfp280d<em1(IMPC)Hmgu>	C57BL/6N-Zfp280d<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696984	M	MP:0010506	prolonged RR interval	Zfp280d<em1(IMPC)Hmgu>/Zfp280d<em1(IMPC)Hmgu>	C57BL/6N-Zfp280d<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696984	M	MP:0005343	increased circulating aspartate transaminase level	Zfp280d<em1(IMPC)Hmgu>/Zfp280d<em1(IMPC)Hmgu>	C57BL/6N-Zfp280d<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6696985	M	MP:0000274	enlarged heart	Zfp474<em1(IMPC)Ccpcz>/Zfp474<em1(IMPC)Ccpcz>	C57BL/6N-Zfp474<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696985	M	MP:0001147	small testis	Zfp474<em1(IMPC)Ccpcz>/Zfp474<em1(IMPC)Ccpcz>	C57BL/6N-Zfp474<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696985	M	MP:0000219	increased neutrophil cell number	Zfp474<em1(IMPC)Ccpcz>/Zfp474<em1(IMPC)Ccpcz>	C57BL/6N-Zfp474<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696985	M	MP:0005016	decreased lymphocyte cell number	Zfp474<em1(IMPC)Ccpcz>/Zfp474<em1(IMPC)Ccpcz>	C57BL/6N-Zfp474<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696985	M	MP:0010067	increased red blood cell distribution width	Zfp474<em1(IMPC)Ccpcz>/Zfp474<em1(IMPC)Ccpcz>	C57BL/6N-Zfp474<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696985	M	MP:0000266	abnormal heart morphology	Zfp474<em1(IMPC)Ccpcz>/Zfp474<em1(IMPC)Ccpcz>	C57BL/6N-Zfp474<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696985	M	MP:0001146	abnormal testis morphology	Zfp474<em1(IMPC)Ccpcz>/Zfp474<em1(IMPC)Ccpcz>	C57BL/6N-Zfp474<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696985	M	MP:0005011	increased eosinophil cell number	Zfp474<em1(IMPC)Ccpcz>/Zfp474<em1(IMPC)Ccpcz>	C57BL/6N-Zfp474<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6696986	M	MP:0001925	male infertility	Zfp541<em1(IMPC)J>/Zfp541<em1(IMPC)J>	C57BL/6NJ-Zfp541<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696986	F	MP:0010506	prolonged RR interval	Zfp541<em1(IMPC)J>/Zfp541<em1(IMPC)J>	C57BL/6NJ-Zfp541<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696987	M	MP:0005333	decreased heart rate	Zfp593<em1(IMPC)J>/Zfp593<em1(IMPC)J>	C57BL/6NJ-Zfp593<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696987	M	MP:0010024	increased total body fat amount	Zfp593<em1(IMPC)J>/Zfp593<em1(IMPC)J>	C57BL/6NJ-Zfp593<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696987	M	MP:0003961	decreased lean body mass	Zfp593<em1(IMPC)J>/Zfp593<em1(IMPC)J>	C57BL/6NJ-Zfp593<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696987	F	MP:0001566	increased circulating phosphate level	Zfp593<em1(IMPC)J>/Zfp593<em1(IMPC)J>	C57BL/6NJ-Zfp593<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696987	M	MP:0010124	decreased bone mineral content	Zfp593<em1(IMPC)J>/Zfp593<em1(IMPC)J>	C57BL/6NJ-Zfp593<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696987	F	MP:0001402	decreased locomotor activity	Zfp593<em1(IMPC)J>/Zfp593<em1(IMPC)J>	C57BL/6NJ-Zfp593<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696987	M	MP:0000063	decreased bone mineral density	Zfp593<em1(IMPC)J>/Zfp593<em1(IMPC)J>	C57BL/6NJ-Zfp593<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6696987	M	MP:0002834	decreased heart weight	Zfp593<em1(IMPC)J>/Zfp593<em1(IMPC)J>	C57BL/6NJ-Zfp593<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6704951	F	MP:0008994	early vaginal opening	Mkrn3<em1Rhu>/Mkrn3<+>	involves: C57BL/6	N	34692086
MGI:6704951	F	MP:0001927	abnormal estrous cycle	Mkrn3<em1Rhu>/Mkrn3<+>	involves: C57BL/6	N	34692086
MGI:6704951	M	MP:0031399	early balanopreputial separation	Mkrn3<em1Rhu>/Mkrn3<+>	involves: C57BL/6	N	34692086
MGI:6704951	M	MP:0001262	decreased body weight	Mkrn3<em1Rhu>/Mkrn3<+>	involves: C57BL/6	N	34692086
MGI:6711107	M	MP:0005452	abnormal adipose tissue amount	Tchp<tm1Inag>/Tchp<tm1Inag>	B6.129P2-Tchp<tm1Inag>	N	33691104
MGI:6711107	M	MP:0005179	decreased circulating cholesterol level	Tchp<tm1Inag>/Tchp<tm1Inag>	B6.129P2-Tchp<tm1Inag>	N	33691104
MGI:6711107	M	MP:0002644	decreased circulating triglyceride level	Tchp<tm1Inag>/Tchp<tm1Inag>	B6.129P2-Tchp<tm1Inag>	N	33691104
MGI:6711107	M	MP:0009269	decreased fat cell size	Tchp<tm1Inag>/Tchp<tm1Inag>	B6.129P2-Tchp<tm1Inag>	N	33691104
MGI:6711107	M	MP:0011167	abnormal adipose tissue development	Tchp<tm1Inag>/Tchp<tm1Inag>	B6.129P2-Tchp<tm1Inag>	N	33691104
MGI:6711107	M	MP:0005670	abnormal white adipose tissue physiology	Tchp<tm1Inag>/Tchp<tm1Inag>	B6.129P2-Tchp<tm1Inag>	N	33691104
MGI:6711107	M	MP:0005533	increased body temperature	Tchp<tm1Inag>/Tchp<tm1Inag>	B6.129P2-Tchp<tm1Inag>	N	33691104
MGI:6711107	M	MP:0005659	decreased susceptibility to diet-induced obesity	Tchp<tm1Inag>/Tchp<tm1Inag>	B6.129P2-Tchp<tm1Inag>	N	33691104
MGI:6711107	M	MP:0011168	abnormal fat cell differentiation	Tchp<tm1Inag>/Tchp<tm1Inag>	B6.129P2-Tchp<tm1Inag>	N	33691104
MGI:6711107	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Tchp<tm1Inag>/Tchp<tm1Inag>	B6.129P2-Tchp<tm1Inag>	N	33691104
MGI:6711266	M	MP:0002687	oligozoospermia	Tslrn1<em1Cwr>/Y	C57BL/6J-Tslrn1<em1Cwr>	N	29044429
MGI:6711266	M	MP:0005389	reproductive system phenotype	Tslrn1<em1Cwr>/Y	C57BL/6J-Tslrn1<em1Cwr>	Y	29044429
MGI:6711266	M	MP:0005378	growth/size/body region phenotype	Tslrn1<em1Cwr>/Y	C57BL/6J-Tslrn1<em1Cwr>	Y	29044429
MGI:6711268	M	MP:0005389	reproductive system phenotype	Tslrn1<em2Cwr>/Y	C57BL/6J-Tslrn1<em2Cwr>	Y	29044429
MGI:6711268	M	MP:0002687	oligozoospermia	Tslrn1<em2Cwr>/Y	C57BL/6J-Tslrn1<em2Cwr>	N	29044429
MGI:6711268	M	MP:0005378	growth/size/body region phenotype	Tslrn1<em2Cwr>/Y	C57BL/6J-Tslrn1<em2Cwr>	Y	29044429
MGI:6711502	M	MP:0013298	increased susceptibility to colitis induced morbidity/mortality	Scgn<em1Ezb>/Scgn<em1Ezb>	C57BL/6-Scgn<em1Ezb>	N	31663849
MGI:6711504	M	MP:0013298	increased susceptibility to colitis induced morbidity/mortality	Scgn<em2Ezb>/Scgn<em2Ezb>	C57BL/6-Scgn<em2Ezb>	N	31663849
MGI:6711591	M	MP:0020869	immotile sperm	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0008545	absent sperm flagellum	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0009834	abnormal sperm annulus morphology	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0001922	reduced male fertility	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0020451	decreased sperm progressive motility	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0005578	teratozoospermia	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0002216	abnormal seminiferous tubule morphology	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0031408	multi-headed sperm	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0005376	homeostasis/metabolism phenotype	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	Y	33913480
MGI:6711591	M	MP:0002675	asthenozoospermia	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0009838	abnormal sperm axoneme morphology	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0001925	male infertility	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0009282	decreased hyperactivated sperm motility	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0009839	multiflagellated sperm	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0001935	decreased litter size	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0006380	abnormal spermatid morphology	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711591	M	MP:0009833	absent sperm mitochondrial sheath	Prss50<em1Cajj>/Prss50<em1Cajj>	involves: C57BL/6J	N	33913480
MGI:6711594	M	MP:0000242	impaired fertilization	Spata3<em1Sbbx>/Spata3<em1Sbbx>	C57BL/6J-Spata3<em1Sbbx>	N	33669425
MGI:6711594	M	MP:0005578	teratozoospermia	Spata3<em1Sbbx>/Spata3<em1Sbbx>	C57BL/6J-Spata3<em1Sbbx>	N	33669425
MGI:6711594	M	MP:0009231	detached acrosome	Spata3<em1Sbbx>/Spata3<em1Sbbx>	C57BL/6J-Spata3<em1Sbbx>	N	33669425
MGI:6711613	M	MP:0002675	asthenozoospermia	Mrnip<em1Nju>/Mrnip<em1Nju>	involves: CD-1	N	33689881
MGI:6711613	M	MP:0001156	abnormal spermatogenesis	Mrnip<em1Nju>/Mrnip<em1Nju>	involves: CD-1	N	33689881
MGI:6711613	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Mrnip<em1Nju>/Mrnip<em1Nju>	involves: CD-1	N	33689881
MGI:6711613	M	MP:0004852	decreased testis weight	Mrnip<em1Nju>/Mrnip<em1Nju>	involves: CD-1	N	33689881
MGI:6711613	M	MP:0001922	reduced male fertility	Mrnip<em1Nju>/Mrnip<em1Nju>	involves: CD-1	N	33689881
MGI:6711613	M	MP:0001147	small testis	Mrnip<em1Nju>/Mrnip<em1Nju>	involves: CD-1	N	33689881
MGI:6711613	M	MP:0001935	decreased litter size	Mrnip<em1Nju>/Mrnip<em1Nju>	involves: CD-1	N	33689881
MGI:6711613	M	MP:0001153	small seminiferous tubules	Mrnip<em1Nju>/Mrnip<em1Nju>	involves: CD-1	N	33689881
MGI:6711613	M	MP:0009451	abnormal chromosomal synapsis	Mrnip<em1Nju>/Mrnip<em1Nju>	involves: CD-1	N	33689881
MGI:6711613	M	MP:0002687	oligozoospermia	Mrnip<em1Nju>/Mrnip<em1Nju>	involves: CD-1	N	33689881
MGI:6711613	M	MP:0005169	abnormal male meiosis	Mrnip<em1Nju>/Mrnip<em1Nju>	involves: CD-1	N	33689881
MGI:6711645	M	MP:0009238	coiled sperm flagellum	Lcn8<em1Jgao>/Lcn8<em1Jgao>	C57BL/6-Lcn8<em1Jgao>	N	33631677
MGI:6711645	M	MP:0013288	premature acrosome reaction	Lcn8<em1Jgao>/Lcn8<em1Jgao>	C57BL/6-Lcn8<em1Jgao>	N	33631677
MGI:6711645	M	MP:0005578	teratozoospermia	Lcn8<em1Jgao>/Lcn8<em1Jgao>	C57BL/6-Lcn8<em1Jgao>	N	33631677
MGI:6711645	M	MP:0020451	decreased sperm progressive motility	Lcn8<em1Jgao>/Lcn8<em1Jgao>	C57BL/6-Lcn8<em1Jgao>	N	33631677
MGI:6711645	M	MP:0002675	asthenozoospermia	Lcn8<em1Jgao>/Lcn8<em1Jgao>	C57BL/6-Lcn8<em1Jgao>	N	33631677
MGI:6711645	M	MP:0009230	abnormal sperm head morphology	Lcn8<em1Jgao>/Lcn8<em1Jgao>	C57BL/6-Lcn8<em1Jgao>	N	33631677
MGI:6711645	M	MP:0009234	absent sperm head	Lcn8<em1Jgao>/Lcn8<em1Jgao>	C57BL/6-Lcn8<em1Jgao>	N	33631677
MGI:6711645	M	MP:0005389	reproductive system phenotype	Lcn8<em1Jgao>/Lcn8<em1Jgao>	C57BL/6-Lcn8<em1Jgao>	Y	33631677
MGI:6711647	M	MP:0005389	reproductive system phenotype	Lcn9<em1Jgao>/Lcn9<em1Jgao>	C57BL/6-Lcn9<em1Jgao>	Y	33631677
MGI:6711805	M	MP:0001392	abnormal locomotor behavior	St8sia3<em1Yich>/St8sia3<em1Yich>	C57BL/6JNarl-St8sia3<em1Yich>	N	31455764
MGI:6711805	M	MP:0013246	abnormal peptide metabolism	St8sia3<em1Yich>/St8sia3<em1Yich>	C57BL/6JNarl-St8sia3<em1Yich>	N	31455764
MGI:6711807	M	MP:0013246	abnormal peptide metabolism	St8sia3<em2Yich>/St8sia3<em2Yich>	C57BL/6JNarl-St8sia3<em2Yich>	N	31455764
MGI:6711807	M	MP:0001392	abnormal locomotor behavior	St8sia3<em2Yich>/St8sia3<em2Yich>	C57BL/6JNarl-St8sia3<em2Yich>	N	31455764
MGI:6711809	M	MP:0001392	abnormal locomotor behavior	St8sia3<em3Yich>/St8sia3<em3Yich>	C57BL/6JNarl-St8sia3<em3Yich>	N	31455764
MGI:6711809	M	MP:0013246	abnormal peptide metabolism	St8sia3<em3Yich>/St8sia3<em3Yich>	C57BL/6JNarl-St8sia3<em3Yich>	N	31455764
MGI:6712184	F	MP:0003699	abnormal female reproductive system physiology	Gm13030<em1Ploen>/Gm13030<em1Ploen>	C57BL/6N-Gm13030<em1Ploen>	N	31436535
MGI:6712243	F	MP:0004805	absent oocytes	Rps26<tm1.1Jzc>/Rps26<tm1.1Jzc>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J	N	30451825
MGI:6712243	F	MP:0031020	premature ovarian failure	Rps26<tm1.1Jzc>/Rps26<tm1.1Jzc>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J	N	30451825
MGI:6712243	F	MP:0001926	female infertility	Rps26<tm1.1Jzc>/Rps26<tm1.1Jzc>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J	N	30451825
MGI:6712243	F	MP:0001130	abnormal ovarian folliculogenesis	Rps26<tm1.1Jzc>/Rps26<tm1.1Jzc>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J	N	30451825
MGI:6712243	F	MP:0001127	small ovary	Rps26<tm1.1Jzc>/Rps26<tm1.1Jzc>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J	N	30451825
MGI:6712243	F	MP:0001125	abnormal oocyte morphology	Rps26<tm1.1Jzc>/Rps26<tm1.1Jzc>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J	N	30451825
MGI:6712243	F	MP:0008871	abnormal ovarian follicle number	Rps26<tm1.1Jzc>/Rps26<tm1.1Jzc>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J	N	30451825
MGI:6712246	F	MP:0001125	abnormal oocyte morphology	Rps26<tm1.1Jzc>/Rps26<tm1.1Jzc>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6J	N	30451825
MGI:6712246	F	MP:0001129	impaired ovarian folliculogenesis	Rps26<tm1.1Jzc>/Rps26<tm1.1Jzc>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6J	N	30451825
MGI:6712246	F	MP:0001926	female infertility	Rps26<tm1.1Jzc>/Rps26<tm1.1Jzc>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6J	N	30451825
MGI:6712730	M	MP:0001262	decreased body weight	Zfyve27<tm1Kei>/Zfyve27<tm1Kei>	B6.129P2-Zfyve27<tm1Kei>	N	33172474
MGI:6712730	M	MP:0005386	behavior/neurological phenotype	Zfyve27<tm1Kei>/Zfyve27<tm1Kei>	B6.129P2-Zfyve27<tm1Kei>	Y	33172474
MGI:6712730	M	MP:0001265	decreased body size	Zfyve27<tm1Kei>/Zfyve27<tm1Kei>	B6.129P2-Zfyve27<tm1Kei>	N	33172474
MGI:6712730	M	MP:0002573	behavioral despair	Zfyve27<tm1Kei>/Zfyve27<tm1Kei>	B6.129P2-Zfyve27<tm1Kei>	N	33172474
MGI:6712730	M	MP:0009456	impaired cued conditioning behavior	Zfyve27<tm1Kei>/Zfyve27<tm1Kei>	B6.129P2-Zfyve27<tm1Kei>	N	33172474
MGI:6712730	M	MP:0001489	decreased startle reflex	Zfyve27<tm1Kei>/Zfyve27<tm1Kei>	B6.129P2-Zfyve27<tm1Kei>	N	33172474
MGI:6712730	M	MP:0001399	hyperactivity	Zfyve27<tm1Kei>/Zfyve27<tm1Kei>	B6.129P2-Zfyve27<tm1Kei>	N	33172474
MGI:6712730	M	MP:0004924	abnormal behavior	Zfyve27<tm1Kei>/Zfyve27<tm1Kei>	B6.129P2-Zfyve27<tm1Kei>	N	33172474
MGI:6712730	M	MP:0003631	nervous system phenotype	Zfyve27<tm1Kei>/Zfyve27<tm1Kei>	B6.129P2-Zfyve27<tm1Kei>	Y	33172474
MGI:6713575	F	MP:0005140	decreased cardiac muscle contractility	Tg(Myh6-MYH7B)#Lnwd/0	C57BL/6-Tg(Myh6-MYH7B)#Lnwd	N	31364453
MGI:6713575	F	MP:0003913	increased heart right ventricle weight	Tg(Myh6-MYH7B)#Lnwd/0	C57BL/6-Tg(Myh6-MYH7B)#Lnwd	N	31364453
MGI:6713575	M	MP:0005140	decreased cardiac muscle contractility	Tg(Myh6-MYH7B)#Lnwd/0	C57BL/6-Tg(Myh6-MYH7B)#Lnwd	N	31364453
MGI:6713575	F	MP:0002753	dilated heart left ventricle	Tg(Myh6-MYH7B)#Lnwd/0	C57BL/6-Tg(Myh6-MYH7B)#Lnwd	N	31364453
MGI:6713575	M	MP:0002753	dilated heart left ventricle	Tg(Myh6-MYH7B)#Lnwd/0	C57BL/6-Tg(Myh6-MYH7B)#Lnwd	N	31364453
MGI:6714084	F	MP:0008948	decreased neuron number	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	involves: 129P2/OlaHsd * C57BL/6	N	31883536
MGI:6714084	F	MP:0020448	increased microglial cell activation	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	involves: 129P2/OlaHsd * C57BL/6	N	31883536
MGI:6714084	F	MP:0008560	increased tumor necrosis factor secretion	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	involves: 129P2/OlaHsd * C57BL/6	N	31883536
MGI:6714084	F	MP:0008657	increased interleukin-1 beta secretion	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	involves: 129P2/OlaHsd * C57BL/6	N	31883536
MGI:6714084	F	MP:0005386	behavior/neurological phenotype	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	involves: 129P2/OlaHsd * C57BL/6	Y	31883536
MGI:6714084	F	MP:0001846	increased inflammatory response	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	involves: 129P2/OlaHsd * C57BL/6	N	31883536
MGI:6714084	F	MP:0008414	abnormal spatial reference memory	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	involves: 129P2/OlaHsd * C57BL/6	N	31883536
MGI:6714084	F	MP:0005319	abnormal enzyme/coenzyme level	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	involves: 129P2/OlaHsd * C57BL/6	N	31883536
MGI:6714150	F	MP:0030278	thick neurocranium	Naa10<tm1Jprk>/Naa10<tm1Jprk>	B6.129P2-Naa10<tm1Jprk>	N	25376646
MGI:6714150	F	MP:0010875	increased bone volume	Naa10<tm1Jprk>/Naa10<tm1Jprk>	B6.129P2-Naa10<tm1Jprk>	N	25376646
MGI:6714150	F	MP:0005006	abnormal osteoblast physiology	Naa10<tm1Jprk>/Naa10<tm1Jprk>	B6.129P2-Naa10<tm1Jprk>	N	25376646
MGI:6714150	F	MP:0000062	increased bone mineral density	Naa10<tm1Jprk>/Naa10<tm1Jprk>	B6.129P2-Naa10<tm1Jprk>	N	25376646
MGI:6714150	F	MP:0002113	abnormal skeleton development	Naa10<tm1Jprk>/Naa10<tm1Jprk>	B6.129P2-Naa10<tm1Jprk>	N	25376646
MGI:6714150	F	MP:0000074	abnormal neurocranium morphology	Naa10<tm1Jprk>/Naa10<tm1Jprk>	B6.129P2-Naa10<tm1Jprk>	N	25376646
MGI:6714150	F	MP:0011710	enhanced osteoblast differentiation	Naa10<tm1Jprk>/Naa10<tm1Jprk>	B6.129P2-Naa10<tm1Jprk>	N	25376646
MGI:6715154	F	MP:0020395	abnormal response to social novelty	Trappc9<em1Xyli>/Trappc9<em1Xyli>	C57BL/6J-Trappc9<em1Xyli>	N	33208359
MGI:6715154	M	MP:0005655	increased aggression	Trappc9<em1Xyli>/Trappc9<em1Xyli>	C57BL/6J-Trappc9<em1Xyli>	N	33208359
MGI:6715154	F	MP:0001923	reduced female fertility	Trappc9<em1Xyli>/Trappc9<em1Xyli>	C57BL/6J-Trappc9<em1Xyli>	N	33208359
MGI:6715154	F	MP:0003461	abnormal response to novel object	Trappc9<em1Xyli>/Trappc9<em1Xyli>	C57BL/6J-Trappc9<em1Xyli>	N	33208359
MGI:6715154	M	MP:0001925	male infertility	Trappc9<em1Xyli>/Trappc9<em1Xyli>	C57BL/6J-Trappc9<em1Xyli>	N	33208359
MGI:6715255	M	MP:0003059	decreased insulin secretion	Nnat<tm1.2Geno>/Nnat<+>	either: 129S2(Cg)-Nnat<tm1.2Geno> or B6.129S2(Cg)-Nnat<tm1.2Geno>	N	29864031
MGI:6715255	M	MP:0005378	growth/size/body region phenotype	Nnat<tm1.2Geno>/Nnat<+>	either: 129S2(Cg)-Nnat<tm1.2Geno> or B6.129S2(Cg)-Nnat<tm1.2Geno>	Y	29864031
MGI:6715255	M	MP:0005386	behavior/neurological phenotype	Nnat<tm1.2Geno>/Nnat<+>	either: 129S2(Cg)-Nnat<tm1.2Geno> or B6.129S2(Cg)-Nnat<tm1.2Geno>	Y	29864031
MGI:6715255	M	MP:0002079	increased circulating insulin level	Nnat<tm1.2Geno>/Nnat<+>	either: 129S2(Cg)-Nnat<tm1.2Geno> or B6.129S2(Cg)-Nnat<tm1.2Geno>	N	29864031
MGI:6715340	M	MP:0020395	abnormal response to social novelty	Fmr1<tm1.1Ics>/Fmr1<tm1.1Ics>	C57BL/6-Fmr1<tm1.1Ics>	N	33692361
MGI:6715340	M	MP:0001473	reduced long-term potentiation	Fmr1<tm1.1Ics>/Fmr1<tm1.1Ics>	C57BL/6-Fmr1<tm1.1Ics>	N	33692361
MGI:6715351	F	MP:0010026	decreased liver cholesterol level	Dhcr24<tm1c(EUCOMM)Wtsi>/Dhcr24<tm1c(EUCOMM)Wtsi>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	B6.Cg-Dhcr24<tm1c(EUCOMM)Wtsi> Speer6-ps1<Tg(Alb-cre)21Mgn>	N	33524375
MGI:6716813	M	MP:0005659	decreased susceptibility to diet-induced obesity	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	N	33691105
MGI:6716813	M	MP:0005668	decreased circulating leptin level	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	N	33691105
MGI:6716813	M	MP:0002891	increased insulin sensitivity	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	N	33691105
MGI:6716813	M	MP:0009289	decreased epididymal fat pad weight	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	N	33691105
MGI:6716813	M	MP:0005375	adipose tissue phenotype	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	Y	33691105
MGI:6716813	M	MP:0004889	increased energy expenditure	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	N	33691105
MGI:6716813	M	MP:0009293	decreased inguinal fat pad weight	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	N	33691105
MGI:6716813	M	MP:0009299	decreased mesenteric fat pad weight	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	N	33691105
MGI:6716813	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	N	33691105
MGI:6716813	M	MP:0009305	decreased retroperitoneal fat pad weight	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	N	33691105
MGI:6716813	M	MP:0002727	decreased circulating insulin level	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	N	33691105
MGI:6716813	M	MP:0005376	homeostasis/metabolism phenotype	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	Y	33691105
MGI:6716813	M	MP:0005292	improved glucose tolerance	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	N	33691105
MGI:6716813	M	MP:0011167	abnormal adipose tissue development	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	N	33691105
MGI:6716813	M	MP:0005670	abnormal white adipose tissue physiology	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>	B6J.B6N-Adig<tm1.1(KOMP)Vlcg>	N	33691105
MGI:6716820	M	MP:0001262	decreased body weight	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>,Lep<ob>/Lep<ob>	B6.Cg-Adig<tm1.1(KOMP)Vlcg> Lep<ob>	N	33691105
MGI:6716820	M	MP:0005293	impaired glucose tolerance	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>,Lep<ob>/Lep<ob>	B6.Cg-Adig<tm1.1(KOMP)Vlcg> Lep<ob>	N	33691105
MGI:6716820	M	MP:0014143	decreased body fat mass	Adig<tm1.1(KOMP)Vlcg>/Adig<tm1.1(KOMP)Vlcg>,Lep<ob>/Lep<ob>	B6.Cg-Adig<tm1.1(KOMP)Vlcg> Lep<ob>	N	33691105
MGI:6717362	F	MP:0001261	obese	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	32877400
MGI:6717362	F	MP:0005293	impaired glucose tolerance	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	32877400
MGI:6717362	F	MP:0001552	increased circulating triglyceride level	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	32877400
MGI:6717362	F	MP:0005178	increased circulating cholesterol level	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	32877400
MGI:6717362	F	MP:0003443	increased circulating glycerol level	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	32877400
MGI:6717362	F	MP:0020396	abnormal social recognition	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	32877400
MGI:6717362	F	MP:0003960	increased lean body mass	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	32877400
MGI:6717362	F	MP:0014142	increased body fat mass	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	32877400
MGI:6717362	F	MP:0000182	increased circulating LDL cholesterol level	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	32877400
MGI:6717362	F	MP:0001556	increased circulating HDL cholesterol level	Trappc9<tm1a(EUCOMM)Wtsi>/Trappc9<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	32877400
MGI:6717414	M	MP:0005389	reproductive system phenotype	Glt6d1<em2Osb>/Glt6d1<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32561905
MGI:6717415	M	MP:0005389	reproductive system phenotype	4930402F06Rik<em1Osb>/4930402F06Rik<em1Osb>,4930568D16Rik<em1Osb>/4930568D16Rik<em1Osb>,Glt6d1<em2Osb>/Glt6d1<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	32561905
MGI:6717416	M	MP:0005389	reproductive system phenotype	4930568D16Rik<em1Osb>/4930568D16Rik<em1Osb>,Glt6d1<em2Osb>/Glt6d1<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32561905
MGI:6717417	M	MP:0005389	reproductive system phenotype	4930568D16Rik<em1Osb>/4930568D16Rik<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32561905
MGI:6717418	M	MP:0005389	reproductive system phenotype	Erich2<em1Osb>/Erich2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32561905
MGI:6717419	M	MP:0005389	reproductive system phenotype	Prss58<em1Osb>/Prss58<em1Osb>	STOCK Prss58<em1Osb>/Osb	N	32561905
MGI:6717420	M	MP:0005389	reproductive system phenotype	Slfnl1<em1Osb>/Slfnl1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32561905
MGI:6717421	M	MP:0005389	reproductive system phenotype	Sppl2c<em1Osb>/Sppl2c<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32561905
MGI:6717422	M	MP:0005389	reproductive system phenotype	Stpg3<em1Osb>/Stpg3<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32561905
MGI:6717423	M	MP:0005389	reproductive system phenotype	Cimip4<em1Osb>/Cimip4<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32561905
MGI:6717424	M	MP:0005389	reproductive system phenotype	Tex36<em1Osb>/Tex36<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32561905
MGI:6718457	M	MP:0005165	increased susceptibility to injury	Igs2<em1(Alb-Golm1)Jdon>/Igs2<+>	involves: C57BL/6N	N	33992711
MGI:6718457	M	MP:0004499	increased incidence of tumors by chemical induction	Igs2<em1(Alb-Golm1)Jdon>/Igs2<+>	involves: C57BL/6N	N	33992711
MGI:6718457	M	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Igs2<em1(Alb-Golm1)Jdon>/Igs2<+>	involves: C57BL/6N	N	33992711
MGI:6718513	M	MP:0005389	reproductive system phenotype	Fyco1<tm1.1Tbph>/Fyco1<tm1.1Tbph>,Tg(NEUROG3-cre)1Herr/0	involves: 129S6/SvEvTac * C57BL/6NCrl	Y	27929729
MGI:6718825	F	MP:0001923	reduced female fertility	Nlrp2<tm1.2Itl>/Nlrp2<tm1.2Itl>	involves: C57BL/6	N	27881734
MGI:6719029	F	MP:0005095	decreased T cell proliferation	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Tg(Lck-cre)548Jxm/0	involves: C57BL/6 * CBA	N	28333124
MGI:6719029	F	MP:0008083	decreased single-positive T cell number	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Tg(Lck-cre)548Jxm/0	involves: C57BL/6 * CBA	N	28333124
MGI:6719029	F	MP:0013772	increased effector memory T-helper cell number	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Tg(Lck-cre)548Jxm/0	involves: C57BL/6 * CBA	N	28333124
MGI:6719029	F	MP:0008567	decreased interferon-gamma secretion	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Tg(Lck-cre)548Jxm/0	involves: C57BL/6 * CBA	N	28333124
MGI:6719029	F	MP:0000706	small thymus	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Tg(Lck-cre)548Jxm/0	involves: C57BL/6 * CBA	N	28333124
MGI:6719029	F	MP:0000715	decreased thymocyte number	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Tg(Lck-cre)548Jxm/0	involves: C57BL/6 * CBA	N	28333124
MGI:6719029	F	MP:0004956	decreased thymus weight	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Tg(Lck-cre)548Jxm/0	involves: C57BL/6 * CBA	N	28333124
MGI:6719029	F	MP:0001823	thymus hypoplasia	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Tg(Lck-cre)548Jxm/0	involves: C57BL/6 * CBA	N	28333124
MGI:6719029	F	MP:0001828	abnormal T cell activation	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Tg(Lck-cre)548Jxm/0	involves: C57BL/6 * CBA	N	28333124
MGI:6719029	F	MP:0009541	increased thymocyte apoptosis	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Tg(Lck-cre)548Jxm/0	involves: C57BL/6 * CBA	N	28333124
MGI:6719029	F	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number	Bcap31<tm1.1Bwang>/Bcap31<tm1.1Bwang>,Tg(Lck-cre)548Jxm/0	involves: C57BL/6 * CBA	N	28333124
MGI:6719209	M	MP:0008537	increased susceptibility to induced colitis	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0008566	increased interferon-gamma secretion	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0010180	increased susceptibility to weight loss	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0013956	decreased colon length	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0009314	increased colon adenocarcinoma incidence	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0004952	increased spleen weight	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0003674	oxidative stress	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0003957	abnormal nitric oxide homeostasis	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0008560	increased tumor necrosis factor secretion	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0002442	abnormal leukocyte physiology	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0009310	increased large intestine adenocarcinoma incidence	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0013663	increased myeloid cell number	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0002444	abnormal T cell physiology	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0004499	increased incidence of tumors by chemical induction	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0010155	abnormal intestine physiology	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6719209	M	MP:0000691	enlarged spleen	Rnf20<Gt(RRJ249)Byg>/Rnf20<+>	involves: 129P2/OlaHsd	N	26854224
MGI:6720272	M	MP:0002912	abnormal excitatory postsynaptic potential	Ythdf1<em1Chhe>/Ythdf1<em1Chhe>	B6.Cg-Ythdf1<em1Chhe>	N	30401835
MGI:6720272	M	MP:0009940	abnormal hippocampus pyramidal cell morphology	Ythdf1<em1Chhe>/Ythdf1<em1Chhe>	B6.Cg-Ythdf1<em1Chhe>	N	30401835
MGI:6720272	M	MP:0001900	impaired synaptic plasticity	Ythdf1<em1Chhe>/Ythdf1<em1Chhe>	B6.Cg-Ythdf1<em1Chhe>	N	30401835
MGI:6720272	M	MP:0003631	nervous system phenotype	Ythdf1<em1Chhe>/Ythdf1<em1Chhe>	B6.Cg-Ythdf1<em1Chhe>	Y	30401835
MGI:6720272	M	MP:0020508	decreased dendritic spine density	Ythdf1<em1Chhe>/Ythdf1<em1Chhe>	B6.Cg-Ythdf1<em1Chhe>	N	30401835
MGI:6720272	M	MP:0012307	impaired spatial learning	Ythdf1<em1Chhe>/Ythdf1<em1Chhe>	B6.Cg-Ythdf1<em1Chhe>	N	30401835
MGI:6720272	M	MP:0009454	impaired contextual conditioning behavior	Ythdf1<em1Chhe>/Ythdf1<em1Chhe>	B6.Cg-Ythdf1<em1Chhe>	N	30401835
MGI:6720272	M	MP:0004753	abnormal miniature excitatory postsynaptic currents	Ythdf1<em1Chhe>/Ythdf1<em1Chhe>	B6.Cg-Ythdf1<em1Chhe>	N	30401835
MGI:6720272	M	MP:0005386	behavior/neurological phenotype	Ythdf1<em1Chhe>/Ythdf1<em1Chhe>	B6.Cg-Ythdf1<em1Chhe>	Y	30401835
MGI:6720272	M	MP:0014252	abnormal paired-pulse ratio	Ythdf1<em1Chhe>/Ythdf1<em1Chhe>	B6.Cg-Ythdf1<em1Chhe>	N	30401835
MGI:6720272	M	MP:0008414	abnormal spatial reference memory	Ythdf1<em1Chhe>/Ythdf1<em1Chhe>	B6.Cg-Ythdf1<em1Chhe>	N	30401835
MGI:6720272	M	MP:0013272	abnormal translation	Ythdf1<em1Chhe>/Ythdf1<em1Chhe>	B6.Cg-Ythdf1<em1Chhe>	N	30401835
MGI:6720272	M	MP:0001473	reduced long-term potentiation	Ythdf1<em1Chhe>/Ythdf1<em1Chhe>	B6.Cg-Ythdf1<em1Chhe>	N	30401835
MGI:6720344	M	MP:0020448	increased microglial cell activation	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720344	M	MP:0002757	decreased vertical activity	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720344	M	MP:0011566	abnormal complement protein level	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720344	M	MP:0000136	abnormal microglial cell morphology	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720344	M	MP:0005386	behavior/neurological phenotype	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	Y	32179479
MGI:6720344	M	MP:0020358	abnormal inhibitory synapse morphology	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720344	M	MP:0000889	abnormal cerebellar molecular layer	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720344	M	MP:0020357	abnormal excitatory synapse morphology	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720344	M	MP:0009940	abnormal hippocampus pyramidal cell morphology	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720344	M	MP:0010050	hypermyelination	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720344	M	MP:0009808	decreased oligodendrocyte number	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720344	M	MP:0001417	decreased exploration in new environment	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720344	M	MP:0020508	decreased dendritic spine density	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720344	M	MP:0001363	increased anxiety-related response	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720344	M	MP:0001405	impaired coordination	Susd4<tm1Lex>/Susd4<tm1Lex>	B6.129S5-Susd4<tm1Lex>	N	32179479
MGI:6720890	M	MP:0005389	reproductive system phenotype	Dnah9<em1Hmd>/Dnah9<em1Hmd>	C57BL/6-Dnah9<em1Hmd>	Y	33347437
MGI:6721005	F	MP:0011448	decreased dopaminergic neuron number	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0005559	increased circulating glucose level	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0000745	tremors	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0011971	increased circulating lactate dehydrogenase level	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0031213	increased eye anterior chamber depth	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0005343	increased circulating aspartate transaminase level	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0005397	hematopoietic system phenotype	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0011967	increased or absent threshold for auditory brainstem response	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0005376	homeostasis/metabolism phenotype	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	Y	34043061
MGI:6721005	F	MP:0008842	lipofuscinosis	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0005543	decreased cornea thickness	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0001326	retina degeneration	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0031391	increased locomotor activity	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0001513	limb grasping	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0008810	increased circulating iron level	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0001260	increased body weight	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0011584	increased alkaline phosphatase activity	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0003354	astrocytosis	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0002642	anisocytosis	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0006325	impaired hearing	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0002229	neurodegeneration	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0011965	decreased total retina thickness	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0001405	impaired coordination	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0005293	impaired glucose tolerance	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0013404	decreased circulating lactate level	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721005	F	MP:0000875	abnormal cerebellar Purkinje cell layer	Wdr45<em1Wrst>/Wdr45<em1Wrst>	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0000218	increased leukocyte cell number	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0001326	retina degeneration	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0011584	increased alkaline phosphatase activity	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0008810	increased circulating iron level	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0005419	decreased circulating serum albumin level	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0003354	astrocytosis	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0001260	increased body weight	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0031391	increased locomotor activity	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0011971	increased circulating lactate dehydrogenase level	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0005376	homeostasis/metabolism phenotype	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	Y	34043061
MGI:6721006	M	MP:0011967	increased or absent threshold for auditory brainstem response	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0005376	homeostasis/metabolism phenotype	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0002229	neurodegeneration	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0005567	decreased circulating total protein level	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0005343	increased circulating aspartate transaminase level	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0031213	increased eye anterior chamber depth	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0005559	increased circulating glucose level	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0011448	decreased dopaminergic neuron number	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0013404	decreased circulating lactate level	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0000875	abnormal cerebellar Purkinje cell layer	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0005564	increased hemoglobin content	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0008805	decreased circulating amylase level	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0006325	impaired hearing	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0001405	impaired coordination	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0011897	decreased circulating unsaturated transferrin level	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0002644	decreased circulating triglyceride level	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0002642	anisocytosis	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0008842	lipofuscinosis	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0020396	abnormal social recognition	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0005543	decreased cornea thickness	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0000745	tremors	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0003131	increased erythrocyte cell number	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721006	M	MP:0001513	limb grasping	Wdr45<em1Wrst>/Y	involves: C57BL/6N * FVB	N	34043061
MGI:6721007	F	MP:0011967	increased or absent threshold for auditory brainstem response	Wdr45<em1Wrst>/Wdr45<+>	involves: C57BL/6N * FVB	N	34043061
MGI:6721007	F	MP:0001405	impaired coordination	Wdr45<em1Wrst>/Wdr45<+>	involves: C57BL/6N * FVB	N	34043061
MGI:6721007	F	MP:0031391	increased locomotor activity	Wdr45<em1Wrst>/Wdr45<+>	involves: C57BL/6N * FVB	N	34043061
MGI:6723807	M	MP:0004543	abnormal sperm physiology	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0006417	rete testis obstruction	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0005159	azoospermia	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	29244804
MGI:6723807	M	MP:0004901	decreased male germ cell number	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	29244804
MGI:6723807	M	MP:0001154	seminiferous tubule degeneration	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	29244804
MGI:6723807	M	MP:0004728	abnormal efferent ductules of testis morphology	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0005389	reproductive system phenotype	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	Y	34085951
MGI:6723807	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0002662	abnormal cauda epididymis morphology	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0006308	enlarged seminiferous tubules	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0008892	abnormal sperm flagellum morphology	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0005578	teratozoospermia	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0002216	abnormal seminiferous tubule morphology	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0002216	abnormal seminiferous tubule morphology	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	29244804
MGI:6723807	M	MP:0001925	male infertility	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0009234	absent sperm head	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0001925	male infertility	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	29244804
MGI:6723807	F	MP:0005389	reproductive system phenotype	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	Y	29244804
MGI:6723807	F	MP:0011644	abnormal oviduct epithelium motile cilium morphology	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	29244804
MGI:6723807	M	MP:0009257	dilated seminiferous tubule	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0006423	dilated rete testis	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0002687	oligozoospermia	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723807	M	MP:0009140	dilated efferent ductule of testis	Cep164<tm1c(EUCOMM)Wtsi>/Cep164<tm1c(EUCOMM)Wtsi>,Tg(FOXJ1-cre)F26Htzm/0	involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N	N	34085951
MGI:6723813	M	MP:0002687	oligozoospermia	Exo5<em1Qsh>/Exo5<em1Qsh>	Not Specified	N	33164760
MGI:6724050	F	MP:0005389	reproductive system phenotype	Prss28<em1Dhap>/Prss28<em1Dhap>	involves: C57BL/6J	Y	33973295
MGI:6724051	F	MP:0005389	reproductive system phenotype	Prss29<em1Dhap>/Prss29<em1Dhap>	involves: C57BL/6J	Y	33973295
MGI:6724052	F	MP:0005389	reproductive system phenotype	Prss28<em1Dhap>/Prss28<em1Dhap>,Prss29<em1Dhap>/Prss29<em1Dhap>	involves: C57BL/6J	Y	33973295
MGI:6724059	M	MP:0001922	reduced male fertility	Dcaf8<em1Rbren>/Dcaf8<em1Rbren>	Not Specified	N	33730447
MGI:6724059	M	MP:0009230	abnormal sperm head morphology	Dcaf8<em1Rbren>/Dcaf8<em1Rbren>	Not Specified	N	33730447
MGI:6724059	M	MP:0031436	decreased copulatory plug deposition	Dcaf8<em1Rbren>/Dcaf8<em1Rbren>	Not Specified	N	33730447
MGI:6724059	M	MP:0020451	decreased sperm progressive motility	Dcaf8<em1Rbren>/Dcaf8<em1Rbren>	Not Specified	N	33730447
MGI:6724062	M	MP:0020451	decreased sperm progressive motility	Trim36<tm1Htan>/Trim36<tm1Htan>	involves: C57BL/6	N	32311190
MGI:6724062	M	MP:0001925	male infertility	Trim36<tm1Htan>/Trim36<tm1Htan>	involves: C57BL/6	N	32311190
MGI:6724281	M	MP:0001262	decreased body weight	Cfap53<em1Cya>/Cfap53<em1Cya>	involves: C57BL/6 * ICR	N	34124066
MGI:6724281	M	MP:0008892	abnormal sperm flagellum morphology	Cfap53<em1Cya>/Cfap53<em1Cya>	involves: C57BL/6 * ICR	N	34124066
MGI:6724281	M	MP:0008545	absent sperm flagellum	Cfap53<em1Cya>/Cfap53<em1Cya>	involves: C57BL/6 * ICR	N	34124066
MGI:6724281	M	MP:0001156	abnormal spermatogenesis	Cfap53<em1Cya>/Cfap53<em1Cya>	involves: C57BL/6 * ICR	N	34124066
MGI:6724281	M	MP:0009838	abnormal sperm axoneme morphology	Cfap53<em1Cya>/Cfap53<em1Cya>	involves: C57BL/6 * ICR	N	34124066
MGI:6724281	M	MP:0009239	short sperm flagellum	Cfap53<em1Cya>/Cfap53<em1Cya>	involves: C57BL/6 * ICR	N	34124066
MGI:6724281	M	MP:0001925	male infertility	Cfap53<em1Cya>/Cfap53<em1Cya>	involves: C57BL/6 * ICR	N	34124066
MGI:6724281	M	MP:0009238	coiled sperm flagellum	Cfap53<em1Cya>/Cfap53<em1Cya>	involves: C57BL/6 * ICR	N	34124066
MGI:6724281	M	MP:0002687	oligozoospermia	Cfap53<em1Cya>/Cfap53<em1Cya>	involves: C57BL/6 * ICR	N	34124066
MGI:6724281	M	MP:0009230	abnormal sperm head morphology	Cfap53<em1Cya>/Cfap53<em1Cya>	involves: C57BL/6 * ICR	N	34124066
MGI:6724281	M	MP:0031386	elongated manchette	Cfap53<em1Cya>/Cfap53<em1Cya>	involves: C57BL/6 * ICR	N	34124066
MGI:6724292	M	MP:0005389	reproductive system phenotype	Dnajb8<em1Sbai>/Dnajb8<em1Sbai>	Not Specified	Y	33391882
MGI:6724295	M	MP:0005389	reproductive system phenotype	Hspa1l<em1Nju>/Hspa1l<em1Nju>	C57BL/6-Hspa1l<em1Nju>	Y	32231871
MGI:6724298	M	MP:0009831	abnormal sperm midpiece morphology	Tg(Fsip2)#Nali/0	C57BL/6-Tg(Fsip2)#Nali	N	34125190
MGI:6724298	M	MP:0030603	increased sperm number	Tg(Fsip2)#Nali/0	C57BL/6-Tg(Fsip2)#Nali	N	34125190
MGI:6724298	M	MP:0009240	elongated sperm flagellum	Tg(Fsip2)#Nali/0	C57BL/6-Tg(Fsip2)#Nali	N	34125190
MGI:6724298	M	MP:0009836	abnormal sperm principal piece morphology	Tg(Fsip2)#Nali/0	C57BL/6-Tg(Fsip2)#Nali	N	34125190
MGI:6724302	M	MP:0009239	short sperm flagellum	Fsip2<em1Nali>/Fsip2<em1Nali>	C57BL/6-Fsip2<em1Nali>	N	34125190
MGI:6724302	M	MP:0001925	male infertility	Fsip2<em1Nali>/Fsip2<em1Nali>	C57BL/6-Fsip2<em1Nali>	N	34125190
MGI:6724302	M	MP:0002687	oligozoospermia	Fsip2<em1Nali>/Fsip2<em1Nali>	C57BL/6-Fsip2<em1Nali>	N	34125190
MGI:6724302	M	MP:0030591	absent sperm fibrous sheath	Fsip2<em1Nali>/Fsip2<em1Nali>	C57BL/6-Fsip2<em1Nali>	N	34125190
MGI:6724302	M	MP:0008892	abnormal sperm flagellum morphology	Fsip2<em1Nali>/Fsip2<em1Nali>	C57BL/6-Fsip2<em1Nali>	N	34125190
MGI:6724302	M	MP:0009280	decreased activated sperm motility	Fsip2<em1Nali>/Fsip2<em1Nali>	C57BL/6-Fsip2<em1Nali>	N	34125190
MGI:6724350	M	MP:0005389	reproductive system phenotype	Ddi1<em1Qsh>/Ddi1<em1Qsh>	C57BL/6-Ddi1<em1Qsh>	Y	33092996
MGI:6724556	M	MP:0001147	small testis	Pramel13<em1Dean>/Pramel13<em1Dean>	involves: C57BL/6J * DBA/2J	N	31729367
MGI:6724556	M	MP:0001925	male infertility	Pramel13<em1Dean>/Pramel13<em1Dean>	involves: C57BL/6J * DBA/2J	N	31729367
MGI:6724556	F	MP:0005389	reproductive system phenotype	Pramel13<em1Dean>/Pramel13<em1Dean>	involves: C57BL/6J * DBA/2J	Y	31729367
MGI:6724557	M	MP:0002685	abnormal spermatogonia proliferation	Pramel13<em2Dean>/Pramel13<em2Dean>	involves: C57BL/6J * DBA/2J	N	31729367
MGI:6724557	M	MP:0014052	increased male germ cell apoptosis	Pramel13<em2Dean>/Pramel13<em2Dean>	involves: C57BL/6J * DBA/2J	N	31729367
MGI:6724557	F	MP:0005389	reproductive system phenotype	Pramel13<em2Dean>/Pramel13<em2Dean>	involves: C57BL/6J * DBA/2J	N	31729367
MGI:6724557	M	MP:0005159	azoospermia	Pramel13<em2Dean>/Pramel13<em2Dean>	involves: C57BL/6J * DBA/2J	N	31729367
MGI:6724557	M	MP:0004852	decreased testis weight	Pramel13<em2Dean>/Pramel13<em2Dean>	involves: C57BL/6J * DBA/2J	N	31729367
MGI:6724557	M	MP:0001147	small testis	Pramel13<em2Dean>/Pramel13<em2Dean>	involves: C57BL/6J * DBA/2J	N	31729367
MGI:6724557	M	MP:0001925	male infertility	Pramel13<em2Dean>/Pramel13<em2Dean>	involves: C57BL/6J * DBA/2J	N	31729367
MGI:6724569	F	MP:0005389	reproductive system phenotype	Tulp2<em1Huizh>/Tulp2<em1Huizh>	C57BL/6-Tulp2<em1Huizh>	Y	33763418
MGI:6724569	M	MP:0002687	oligozoospermia	Tulp2<em1Huizh>/Tulp2<em1Huizh>	C57BL/6-Tulp2<em1Huizh>	N	33763418
MGI:6724569	M	MP:0020451	decreased sperm progressive motility	Tulp2<em1Huizh>/Tulp2<em1Huizh>	C57BL/6-Tulp2<em1Huizh>	N	33763418
MGI:6724569	M	MP:0009838	abnormal sperm axoneme morphology	Tulp2<em1Huizh>/Tulp2<em1Huizh>	C57BL/6-Tulp2<em1Huizh>	N	33763418
MGI:6724569	M	MP:0001925	male infertility	Tulp2<em1Huizh>/Tulp2<em1Huizh>	C57BL/6-Tulp2<em1Huizh>	N	33763418
MGI:6724569	M	MP:0013601	increased testis apoptosis	Tulp2<em1Huizh>/Tulp2<em1Huizh>	C57BL/6-Tulp2<em1Huizh>	N	33763418
MGI:6724569	M	MP:0009237	kinked sperm flagellum	Tulp2<em1Huizh>/Tulp2<em1Huizh>	C57BL/6-Tulp2<em1Huizh>	N	33763418
MGI:6724569	M	MP:0011635	abnormal mitochondrial crista morphology	Tulp2<em1Huizh>/Tulp2<em1Huizh>	C57BL/6-Tulp2<em1Huizh>	N	33763418
MGI:6724569	M	MP:0006380	abnormal spermatid morphology	Tulp2<em1Huizh>/Tulp2<em1Huizh>	C57BL/6-Tulp2<em1Huizh>	N	33763418
MGI:6724569	M	MP:0009831	abnormal sperm midpiece morphology	Tulp2<em1Huizh>/Tulp2<em1Huizh>	C57BL/6-Tulp2<em1Huizh>	N	33763418
MGI:6724569	M	MP:0002675	asthenozoospermia	Tulp2<em1Huizh>/Tulp2<em1Huizh>	C57BL/6-Tulp2<em1Huizh>	N	33763418
MGI:6724575	M	MP:0002687	oligozoospermia	Jmy<tm1Smoc>/Jmy<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: 129S * C57BL/6	N	32279424
MGI:6724575	M	MP:0002216	abnormal seminiferous tubule morphology	Jmy<tm1Smoc>/Jmy<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: 129S * C57BL/6	N	32279424
MGI:6724575	M	MP:0001935	decreased litter size	Jmy<tm1Smoc>/Jmy<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: 129S * C57BL/6	N	32279424
MGI:6724575	M	MP:0009233	enlarged sperm head	Jmy<tm1Smoc>/Jmy<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: 129S * C57BL/6	N	32279424
MGI:6724575	M	MP:0020356	abnormal Sertoli cell barrier function	Jmy<tm1Smoc>/Jmy<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: 129S * C57BL/6	N	32279424
MGI:6724575	M	MP:0002675	asthenozoospermia	Jmy<tm1Smoc>/Jmy<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: 129S * C57BL/6	N	32279424
MGI:6724575	M	MP:0020451	decreased sperm progressive motility	Jmy<tm1Smoc>/Jmy<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: 129S * C57BL/6	N	32279424
MGI:6724575	M	MP:0001922	reduced male fertility	Jmy<tm1Smoc>/Jmy<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: 129S * C57BL/6	N	32279424
MGI:6724589	F	MP:0008567	decreased interferon-gamma secretion	Mir378b<em#Yoo>/Mir378b<em#Yoo>	C57BL/6J-Mir378b<em#Yoo>	N	34067003
MGI:6724589	F	MP:0008722	abnormal chemokine secretion	Mir378b<em#Yoo>/Mir378b<em#Yoo>	C57BL/6J-Mir378b<em#Yoo>	N	34067003
MGI:6724589	F	MP:0008664	decreased interleukin-12 secretion	Mir378b<em#Yoo>/Mir378b<em#Yoo>	C57BL/6J-Mir378b<em#Yoo>	N	34067003
MGI:6724589	F	MP:0020186	abnormal susceptibility to bacterial infection	Mir378b<em#Yoo>/Mir378b<em#Yoo>	C57BL/6J-Mir378b<em#Yoo>	N	34067003
MGI:6724589	F	MP:0008561	decreased tumor necrosis factor secretion	Mir378b<em#Yoo>/Mir378b<em#Yoo>	C57BL/6J-Mir378b<em#Yoo>	N	34067003
MGI:6725111	M	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport	Tfb2m<tm1a(KOMP)Wtsi>/Tfb2m<+>,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	28702322
MGI:6725111	M	MP:0006036	abnormal mitochondrial physiology	Tfb2m<tm1a(KOMP)Wtsi>/Tfb2m<+>,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	28702322
MGI:6725111	M	MP:0002727	decreased circulating insulin level	Tfb2m<tm1a(KOMP)Wtsi>/Tfb2m<+>,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	28702322
MGI:6725111	M	MP:0009114	decreased pancreatic beta cell mass	Tfb2m<tm1a(KOMP)Wtsi>/Tfb2m<+>,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	28702322
MGI:6725111	M	MP:0003059	decreased insulin secretion	Tfb2m<tm1a(KOMP)Wtsi>/Tfb2m<+>,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	28702322
MGI:6725111	M	MP:0005293	impaired glucose tolerance	Tfb2m<tm1a(KOMP)Wtsi>/Tfb2m<+>,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	28702322
MGI:6725111	M	MP:0009168	decreased pancreatic islet number	Tfb2m<tm1a(KOMP)Wtsi>/Tfb2m<+>,Tg(Ins2-cre)23Herr/0	involves: C57BL/6J * C57BL/6N * CBA/J	N	28702322
MGI:6725813	M	MP:0001925	male infertility	Tsga10<em2Smoc>/Tsga10<+>	involves: C57BL/6J	N	32790169
MGI:6725815	M	MP:0001925	male infertility	Tsga10<em1Smoc>/Tsga10<+>	involves: C57BL/6J	N	32790169
MGI:6725815	M	MP:0002674	abnormal sperm motility	Tsga10<em1Smoc>/Tsga10<+>	involves: C57BL/6J	N	32790169
MGI:6725815	M	MP:0002673	abnormal sperm number	Tsga10<em1Smoc>/Tsga10<+>	involves: C57BL/6J	N	32790169
MGI:6725815	M	MP:0000242	impaired fertilization	Tsga10<em1Smoc>/Tsga10<+>	involves: C57BL/6J	N	32790169
MGI:6725815	M	MP:0006378	abnormal spermatogonia morphology	Tsga10<em1Smoc>/Tsga10<+>	involves: C57BL/6J	N	32790169
MGI:6726370	M	MP:0005528	decreased renal glomerular filtration rate	Abcg2<em1Omw>/Abcg2<em1Omw>	C57BL/6J-Abcg2<em1Omw>	N	32488095
MGI:6726370	M	MP:0008055	increased urine osmolality	Abcg2<em1Omw>/Abcg2<em1Omw>	C57BL/6J-Abcg2<em1Omw>	N	32488095
MGI:6726370	M	MP:0005627	increased circulating potassium level	Abcg2<em1Omw>/Abcg2<em1Omw>	C57BL/6J-Abcg2<em1Omw>	N	32488095
MGI:6726370	M	MP:0005559	increased circulating glucose level	Abcg2<em1Omw>/Abcg2<em1Omw>	C57BL/6J-Abcg2<em1Omw>	N	32488095
MGI:6726370	M	MP:0002628	hepatic steatosis	Abcg2<em1Omw>/Abcg2<em1Omw>	C57BL/6J-Abcg2<em1Omw>	N	32488095
MGI:6726370	M	MP:0010155	abnormal intestine physiology	Abcg2<em1Omw>/Abcg2<em1Omw>	C57BL/6J-Abcg2<em1Omw>	N	32488095
MGI:6726370	M	MP:0002079	increased circulating insulin level	Abcg2<em1Omw>/Abcg2<em1Omw>	C57BL/6J-Abcg2<em1Omw>	N	32488095
MGI:6726370	M	MP:0006316	increased urine sodium level	Abcg2<em1Omw>/Abcg2<em1Omw>	C57BL/6J-Abcg2<em1Omw>	N	32488095
MGI:6726370	M	MP:0004702	increased circulating insulin-like growth factor I level	Abcg2<em1Omw>/Abcg2<em1Omw>	C57BL/6J-Abcg2<em1Omw>	N	32488095
MGI:6726370	M	MP:0008821	increased blood uric acid level	Abcg2<em1Omw>/Abcg2<em1Omw>	C57BL/6J-Abcg2<em1Omw>	N	32488095
MGI:6726370	M	MP:0002136	abnormal kidney physiology	Abcg2<em1Omw>/Abcg2<em1Omw>	C57BL/6J-Abcg2<em1Omw>	N	32488095
MGI:6727060	M	MP:0006380	abnormal spermatid morphology	Tsga8<em1Ohbo>/Y	C57BL/6-Tsga8<em1Ohbo>	N	33766931
MGI:6727060	M	MP:0009852	increased Sertoli cell phagocytosis	Tsga8<em1Ohbo>/Y	C57BL/6-Tsga8<em1Ohbo>	N	33766931
MGI:6727060	M	MP:0001925	male infertility	Tsga8<em1Ohbo>/Y	C57BL/6-Tsga8<em1Ohbo>	N	33766931
MGI:6727060	M	MP:0005159	azoospermia	Tsga8<em1Ohbo>/Y	C57BL/6-Tsga8<em1Ohbo>	N	33766931
MGI:6727060	M	MP:0001156	abnormal spermatogenesis	Tsga8<em1Ohbo>/Y	C57BL/6-Tsga8<em1Ohbo>	N	33766931
MGI:6727060	M	MP:0005378	growth/size/body region phenotype	Tsga8<em1Ohbo>/Y	C57BL/6-Tsga8<em1Ohbo>	Y	33766931
MGI:6727060	M	MP:0001932	abnormal spermiogenesis	Tsga8<em1Ohbo>/Y	C57BL/6-Tsga8<em1Ohbo>	N	33766931
MGI:6727060	M	MP:0013601	increased testis apoptosis	Tsga8<em1Ohbo>/Y	C57BL/6-Tsga8<em1Ohbo>	N	33766931
MGI:6727060	M	MP:0004852	decreased testis weight	Tsga8<em1Ohbo>/Y	C57BL/6-Tsga8<em1Ohbo>	N	33766931
MGI:6727062	M	MP:0001932	abnormal spermiogenesis	Tsga8<em2Ohbo>/Tsga8<em2Ohbo>	C57BL/6-Tsga8<em2Ohbo>	N	33766931
MGI:6727062	M	MP:0004852	decreased testis weight	Tsga8<em2Ohbo>/Tsga8<em2Ohbo>	C57BL/6-Tsga8<em2Ohbo>	N	33766931
MGI:6727062	M	MP:0001925	male infertility	Tsga8<em2Ohbo>/Tsga8<em2Ohbo>	C57BL/6-Tsga8<em2Ohbo>	N	33766931
MGI:6727062	M	MP:0001156	abnormal spermatogenesis	Tsga8<em2Ohbo>/Tsga8<em2Ohbo>	C57BL/6-Tsga8<em2Ohbo>	N	33766931
MGI:6727062	M	MP:0005378	growth/size/body region phenotype	Tsga8<em2Ohbo>/Tsga8<em2Ohbo>	C57BL/6-Tsga8<em2Ohbo>	Y	33766931
MGI:6727062	M	MP:0005159	azoospermia	Tsga8<em2Ohbo>/Tsga8<em2Ohbo>	C57BL/6-Tsga8<em2Ohbo>	N	33766931
MGI:6727062	M	MP:0013601	increased testis apoptosis	Tsga8<em2Ohbo>/Tsga8<em2Ohbo>	C57BL/6-Tsga8<em2Ohbo>	N	33766931
MGI:6727062	M	MP:0009852	increased Sertoli cell phagocytosis	Tsga8<em2Ohbo>/Tsga8<em2Ohbo>	C57BL/6-Tsga8<em2Ohbo>	N	33766931
MGI:6727062	M	MP:0006380	abnormal spermatid morphology	Tsga8<em2Ohbo>/Tsga8<em2Ohbo>	C57BL/6-Tsga8<em2Ohbo>	N	33766931
MGI:6727110	M	MP:0009237	kinked sperm flagellum	Cfap47<em1Fzh>/Y	C57BL/6-Cfap47<em1Fzh>	N	33472045
MGI:6727110	M	MP:0002675	asthenozoospermia	Cfap47<em1Fzh>/Y	C57BL/6-Cfap47<em1Fzh>	N	33472045
MGI:6727110	F	MP:0005389	reproductive system phenotype	Cfap47<em1Fzh>/Y	C57BL/6-Cfap47<em1Fzh>	Y	33472045
MGI:6727110	M	MP:0030590	abnormal sperm fibrous sheath morphology	Cfap47<em1Fzh>/Y	C57BL/6-Cfap47<em1Fzh>	N	33472045
MGI:6727110	M	MP:0001925	male infertility	Cfap47<em1Fzh>/Y	C57BL/6-Cfap47<em1Fzh>	N	33472045
MGI:6727110	M	MP:0005578	teratozoospermia	Cfap47<em1Fzh>/Y	C57BL/6-Cfap47<em1Fzh>	N	33472045
MGI:6729182	M	MP:0002169	no abnormal phenotype detected	Slx<em1.1Jbmu>/Y	involves: C57BL/6NHsd * DBA/2NHsd * FVB/N	N	31630956
MGI:6729183	M	MP:0001156	abnormal spermatogenesis	Slx<em1.1Jbmu> Slxl1<em1.1Jbmu>/Y	involves: C57BL/6NHsd * DBA/2NHsd * FVB/N	N	31630956
MGI:6729183	M	MP:0002687	oligozoospermia	Slx<em1.1Jbmu> Slxl1<em1.1Jbmu>/Y	involves: C57BL/6NHsd * DBA/2NHsd * FVB/N	N	31630956
MGI:6729183	M	MP:0001925	male infertility	Slx<em1.1Jbmu> Slxl1<em1.1Jbmu>/Y	involves: C57BL/6NHsd * DBA/2NHsd * FVB/N	N	31630956
MGI:6729183	M	MP:0002686	globozoospermia	Slx<em1.1Jbmu> Slxl1<em1.1Jbmu>/Y	involves: C57BL/6NHsd * DBA/2NHsd * FVB/N	N	31630956
MGI:6729183	M	MP:0005578	teratozoospermia	Slx<em1.1Jbmu> Slxl1<em1.1Jbmu>/Y	involves: C57BL/6NHsd * DBA/2NHsd * FVB/N	N	31630956
MGI:6729184	M	MP:0004179	transmission ratio distortion	Slxl1<em1.1Jbmu>/Y	involves: C57BL/6NHsd * DBA/2NHsd * FVB/N	N	31630956
MGI:6729184	M	MP:0005389	reproductive system phenotype	Slxl1<em1.1Jbmu>/Y	involves: C57BL/6NHsd * DBA/2NHsd * FVB/N	Y	31630956
MGI:6729185	M	MP:0005389	reproductive system phenotype	Slxl1<em1.2Jbmu>/Y	involves: C57BL/6NHsd * DBA/2NHsd * FVB/N	Y	31630956
MGI:6729186	M	MP:0004179	transmission ratio distortion	Slx<em1.2Jbmu> Slxl1<em1.2Jbmu>/Y	involves: C57BL/6NHsd * DBA/2NHsd * FVB/N	Y	31630956
MGI:6729187	M	MP:0006009	abnormal neuronal migration	Fgf13<em1Xuzh>/Y	involves: C57BL/6J	N	34184986
MGI:6729187	M	MP:0009937	abnormal neuron differentiation	Fgf13<em1Xuzh>/Y	involves: C57BL/6J	N	34184986
MGI:6729187	M	MP:0009454	impaired contextual conditioning behavior	Fgf13<em1Xuzh>/Y	involves: C57BL/6J	N	34184986
MGI:6729187	M	MP:0002184	abnormal innervation	Fgf13<em1Xuzh>/Y	involves: C57BL/6J	N	34184986
MGI:6729187	M	MP:0008414	abnormal spatial reference memory	Fgf13<em1Xuzh>/Y	involves: C57BL/6J	N	34184986
MGI:6729187	M	MP:0020508	decreased dendritic spine density	Fgf13<em1Xuzh>/Y	involves: C57BL/6J	N	34184986
MGI:6729187	M	MP:0012307	impaired spatial learning	Fgf13<em1Xuzh>/Y	involves: C57BL/6J	N	34184986
MGI:6729187	M	MP:0003651	abnormal axon extension	Fgf13<em1Xuzh>/Y	involves: C57BL/6J	N	34184986
MGI:6729187	M	MP:0003063	increased coping response	Fgf13<em1Xuzh>/Y	involves: C57BL/6J	N	34184986
MGI:6729187	M	MP:0000790	abnormal stratification in cerebral cortex	Fgf13<em1Xuzh>/Y	involves: C57BL/6J	N	34184986
MGI:6729187	M	MP:0009456	impaired cued conditioning behavior	Fgf13<em1Xuzh>/Y	involves: C57BL/6J	N	34184986
MGI:6729732	F	MP:0013375	abnormal sebocyte morphology	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0013391	abnormal Meibomian gland physiology	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0013145	eye discharge	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0003853	dry skin	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0001851	eye inflammation	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0001314	cornea opacity	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0005252	abnormal Meibomian gland morphology	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0005251	blepharitis	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0001340	abnormal eyelid morphology	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0004222	iris synechia	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0001337	dry eyes	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0009935	abnormal Meibomian gland acinus morphology	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0000649	sebaceous gland atrophy	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0006193	conjunctival telangiectasia	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0005542	cornea vascularization	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0005300	abnormal cornea stroma morphology	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0013192	decreased sebaceous gland number	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0001219	thick epidermis	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0010202	focal dorsal hair loss	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0001192	scaly skin	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0006000	abnormal cornea epithelium morphology	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0001312	abnormal cornea morphology	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0001310	abnormal conjunctiva morphology	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0001322	abnormal iris morphology	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0014154	Meibomian gland degeneration	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0011962	increased cornea thickness	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0010699	dilated hair follicle	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0001212	skin lesions	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0014131	abnormal tear film morphology	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729732	F	MP:0008778	abnormal lymphangiogenesis	Awat2<tm1.2Golc>/Awat2<tm1.2Golc>	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0001212	skin lesions	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0006000	abnormal cornea epithelium morphology	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0008778	abnormal lymphangiogenesis	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0000649	sebaceous gland atrophy	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0001337	dry eyes	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0005542	cornea vascularization	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0006193	conjunctival telangiectasia	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0010202	focal dorsal hair loss	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0001219	thick epidermis	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0001192	scaly skin	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0001312	abnormal cornea morphology	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0011962	increased cornea thickness	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0010699	dilated hair follicle	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0013375	abnormal sebocyte morphology	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0013391	abnormal Meibomian gland physiology	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0001851	eye inflammation	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0001314	cornea opacity	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0005251	blepharitis	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0004222	iris synechia	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0005252	abnormal Meibomian gland morphology	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0014131	abnormal tear film morphology	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0014154	Meibomian gland degeneration	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0001322	abnormal iris morphology	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0001310	abnormal conjunctiva morphology	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0005300	abnormal cornea stroma morphology	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0013145	eye discharge	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0013192	decreased sebaceous gland number	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0009935	abnormal Meibomian gland acinus morphology	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0001340	abnormal eyelid morphology	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6729736	M	MP:0003853	dry skin	Awat2<tm1.2Golc>/Y	involves: 129 * C57BL/6 * C57BL/6J	N	32851726
MGI:6730374	M	MP:0008907	decreased total fat pad weight	Zfp217<em1Sjia>/Zfp217<+>	involves: C57BL/6J	N	34065474
MGI:6730374	M	MP:0009269	decreased fat cell size	Zfp217<em1Sjia>/Zfp217<+>	involves: C57BL/6J	N	34065474
MGI:6730374	M	MP:0005659	decreased susceptibility to diet-induced obesity	Zfp217<em1Sjia>/Zfp217<+>	involves: C57BL/6J	N	34065474
MGI:6730374	M	MP:0005292	improved glucose tolerance	Zfp217<em1Sjia>/Zfp217<+>	involves: C57BL/6J	N	34065474
MGI:6730374	M	MP:0005459	decreased percent body fat/body weight	Zfp217<em1Sjia>/Zfp217<+>	involves: C57BL/6J	N	34065474
MGI:6730374	M	MP:0008963	increased carbon dioxide production	Zfp217<em1Sjia>/Zfp217<+>	involves: C57BL/6J	N	34065474
MGI:6730374	M	MP:0002891	increased insulin sensitivity	Zfp217<em1Sjia>/Zfp217<+>	involves: C57BL/6J	N	34065474
MGI:6731234	M	MP:0010024	increased total body fat amount	1700008P02Rik<em1(IMPC)J>/1700008P02Rik<em1(IMPC)J>	C57BL/6NJ-1700008P02Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731234	M	MP:0005178	increased circulating cholesterol level	1700008P02Rik<em1(IMPC)J>/1700008P02Rik<em1(IMPC)J>	C57BL/6NJ-1700008P02Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731234	M	MP:0001556	increased circulating HDL cholesterol level	1700008P02Rik<em1(IMPC)J>/1700008P02Rik<em1(IMPC)J>	C57BL/6NJ-1700008P02Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731234	F	MP:0001566	increased circulating phosphate level	1700008P02Rik<em1(IMPC)J>/1700008P02Rik<em1(IMPC)J>	C57BL/6NJ-1700008P02Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731237	M	MP:0001513	limb grasping	Abhd14b<em1(IMPC)J>/Abhd14b<em1(IMPC)J>	C57BL/6NJ-Abhd14b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731237	F	MP:0001392	abnormal locomotor behavior	Abhd14b<em1(IMPC)J>/Abhd14b<em1(IMPC)J>	C57BL/6NJ-Abhd14b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731238	M	MP:0001364	decreased anxiety-related response	Acat1<em1(IMPC)J>/Acat1<em1(IMPC)J>	C57BL/6NJ-Acat1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731239	M	MP:0001146	abnormal testis morphology	Adamts12<em1(IMPC)Mbp>/Adamts12<em1(IMPC)Mbp>	C57BL/6N-Adamts12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731239	M	MP:0001148	enlarged testis	Adamts12<em1(IMPC)Mbp>/Adamts12<em1(IMPC)Mbp>	C57BL/6N-Adamts12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731240	M	MP:0001417	decreased exploration in new environment	Adk<em1(IMPC)Ccpcz>/Adk<+>	C57BL/6N-Adk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731240	M	MP:0002060	abnormal skin morphology	Adk<em1(IMPC)Ccpcz>/Adk<+>	C57BL/6N-Adk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731240	F	MP:0000703	abnormal thymus morphology	Adk<em1(IMPC)Ccpcz>/Adk<+>	C57BL/6N-Adk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731240	M	MP:0011047	increased lung tissue damping	Adk<em1(IMPC)Ccpcz>/Adk<+>	C57BL/6N-Adk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731240	M	MP:0001175	abnormal lung morphology	Adk<em1(IMPC)Ccpcz>/Adk<+>	C57BL/6N-Adk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731240	F	MP:0000709	enlarged thymus	Adk<em1(IMPC)Ccpcz>/Adk<+>	C57BL/6N-Adk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731240	M	MP:0004882	enlarged lung	Adk<em1(IMPC)Ccpcz>/Adk<+>	C57BL/6N-Adk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731240	F	MP:0000689	abnormal spleen morphology	Adk<em1(IMPC)Ccpcz>/Adk<+>	C57BL/6N-Adk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731242	M	MP:0011110	preweaning lethality, incomplete penetrance	AI467606<tm2b(EUCOMM)Wtsi>/AI467606<tm2b(EUCOMM)Wtsi>	C57BL/6N-AI467606<tm2b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6731243	F	MP:0000703	abnormal thymus morphology	Aim2<em1(IMPC)Ccpcz>/Aim2<em1(IMPC)Ccpcz>	C57BL/6N-Aim2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731243	F	MP:0000689	abnormal spleen morphology	Aim2<em1(IMPC)Ccpcz>/Aim2<em1(IMPC)Ccpcz>	C57BL/6N-Aim2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731243	F	MP:0000691	enlarged spleen	Aim2<em1(IMPC)Ccpcz>/Aim2<em1(IMPC)Ccpcz>	C57BL/6N-Aim2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731243	F	MP:0000709	enlarged thymus	Aim2<em1(IMPC)Ccpcz>/Aim2<em1(IMPC)Ccpcz>	C57BL/6N-Aim2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731243	F	MP:0005084	abnormal gallbladder morphology	Aim2<em1(IMPC)Ccpcz>/Aim2<em1(IMPC)Ccpcz>	C57BL/6N-Aim2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731243	M	MP:0002965	increased circulating serum albumin level	Aim2<em1(IMPC)Ccpcz>/Aim2<em1(IMPC)Ccpcz>	C57BL/6N-Aim2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731243	F	MP:0009342	enlarged gallbladder	Aim2<em1(IMPC)Ccpcz>/Aim2<em1(IMPC)Ccpcz>	C57BL/6N-Aim2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0001157	small seminal vesicle	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0001147	small testis	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0000274	enlarged heart	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0000692	small spleen	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0000703	abnormal thymus morphology	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0002059	abnormal seminal vesicle morphology	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0002060	abnormal skin morphology	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0013129	abnormal tooth color	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0030610	absent teeth	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0000709	enlarged thymus	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0000689	abnormal spleen morphology	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0001146	abnormal testis morphology	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0003883	enlarged stomach	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0002100	abnormal tooth morphology	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0005270	abnormal zygomatic bone morphology	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0000266	abnormal heart morphology	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731244	M	MP:0000470	abnormal stomach morphology	Amelx<em1(IMPC)Ccpcz>/Y	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731245	F	MP:0030610	absent teeth	Amelx<em1(IMPC)Ccpcz>/Amelx<em1(IMPC)Ccpcz>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731245	F	MP:0000703	abnormal thymus morphology	Amelx<em1(IMPC)Ccpcz>/Amelx<em1(IMPC)Ccpcz>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731245	F	MP:0011047	increased lung tissue damping	Amelx<em1(IMPC)Ccpcz>/Amelx<em1(IMPC)Ccpcz>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731245	F	MP:0002966	decreased circulating alkaline phosphatase level	Amelx<em1(IMPC)Ccpcz>/Amelx<em1(IMPC)Ccpcz>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731245	F	MP:0000470	abnormal stomach morphology	Amelx<em1(IMPC)Ccpcz>/Amelx<em1(IMPC)Ccpcz>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731245	F	MP:0003883	enlarged stomach	Amelx<em1(IMPC)Ccpcz>/Amelx<em1(IMPC)Ccpcz>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731245	F	MP:0000709	enlarged thymus	Amelx<em1(IMPC)Ccpcz>/Amelx<em1(IMPC)Ccpcz>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731245	F	MP:0001262	decreased body weight	Amelx<em1(IMPC)Ccpcz>/Amelx<em1(IMPC)Ccpcz>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731245	F	MP:0002100	abnormal tooth morphology	Amelx<em1(IMPC)Ccpcz>/Amelx<em1(IMPC)Ccpcz>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731245	F	MP:0013129	abnormal tooth color	Amelx<em1(IMPC)Ccpcz>/Amelx<em1(IMPC)Ccpcz>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731246	M	MP:0001148	enlarged testis	Apbb1ip<em1(IMPC)Ccpcz>/Apbb1ip<em1(IMPC)Ccpcz>	C57BL/6N-Apbb1ip<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731246	M	MP:0001146	abnormal testis morphology	Apbb1ip<em1(IMPC)Ccpcz>/Apbb1ip<em1(IMPC)Ccpcz>	C57BL/6N-Apbb1ip<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731246	M	MP:0004952	increased spleen weight	Apbb1ip<em1(IMPC)Ccpcz>/Apbb1ip<em1(IMPC)Ccpcz>	C57BL/6N-Apbb1ip<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731246	F	MP:0000703	abnormal thymus morphology	Apbb1ip<em1(IMPC)Ccpcz>/Apbb1ip<em1(IMPC)Ccpcz>	C57BL/6N-Apbb1ip<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731246	F	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number	Apbb1ip<em1(IMPC)Ccpcz>/Apbb1ip<em1(IMPC)Ccpcz>	C57BL/6N-Apbb1ip<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731246	F	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number	Apbb1ip<em1(IMPC)Ccpcz>/Apbb1ip<em1(IMPC)Ccpcz>	C57BL/6N-Apbb1ip<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731246	F	MP:0010935	increased airway resistance	Apbb1ip<em1(IMPC)Ccpcz>/Apbb1ip<em1(IMPC)Ccpcz>	C57BL/6N-Apbb1ip<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731246	F	MP:0000709	enlarged thymus	Apbb1ip<em1(IMPC)Ccpcz>/Apbb1ip<em1(IMPC)Ccpcz>	C57BL/6N-Apbb1ip<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731246	M	MP:0003917	increased kidney weight	Apbb1ip<em1(IMPC)Ccpcz>/Apbb1ip<em1(IMPC)Ccpcz>	C57BL/6N-Apbb1ip<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731246	M	MP:0010067	increased red blood cell distribution width	Apbb1ip<em1(IMPC)Ccpcz>/Apbb1ip<em1(IMPC)Ccpcz>	C57BL/6N-Apbb1ip<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731249	M	MP:0010123	increased bone mineral content	Arsj<em1(IMPC)J>/Arsj<em1(IMPC)J>	C57BL/6NJ-Arsj<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731249	M	MP:0002626	increased heart rate	Arsj<em1(IMPC)J>/Arsj<em1(IMPC)J>	C57BL/6NJ-Arsj<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731249	M	MP:0010025	decreased total body fat amount	Arsj<em1(IMPC)J>/Arsj<em1(IMPC)J>	C57BL/6NJ-Arsj<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731249	M	MP:0010507	shortened RR interval	Arsj<em1(IMPC)J>/Arsj<em1(IMPC)J>	C57BL/6NJ-Arsj<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731249	M	MP:0001488	increased startle reflex	Arsj<em1(IMPC)J>/Arsj<em1(IMPC)J>	C57BL/6NJ-Arsj<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731249	M	MP:0003960	increased lean body mass	Arsj<em1(IMPC)J>/Arsj<em1(IMPC)J>	C57BL/6NJ-Arsj<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731249	M	MP:0002833	increased heart weight	Arsj<em1(IMPC)J>/Arsj<em1(IMPC)J>	C57BL/6NJ-Arsj<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731249	M	MP:0000062	increased bone mineral density	Arsj<em1(IMPC)J>/Arsj<em1(IMPC)J>	C57BL/6NJ-Arsj<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731250	F	MP:0011965	decreased total retina thickness	Atp13a4<em1(IMPC)Bay>/Atp13a4<em1(IMPC)Bay>	C57BL/6N-Atp13a4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731250	F	MP:0003731	abnormal retina outer nuclear layer morphology	Atp13a4<em1(IMPC)Bay>/Atp13a4<em1(IMPC)Bay>	C57BL/6N-Atp13a4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731254	M	MP:0005178	increased circulating cholesterol level	Banp<em1(IMPC)J>/Banp<+>	C57BL/6NJ-Banp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731255	M	MP:0010379	decreased respiratory quotient	Bbip1<em1(IMPC)Ccpcz>/Bbip1<+>	C57BL/6N-Bbip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731255	M	MP:0001944	abnormal pancreas morphology	Bbip1<em1(IMPC)Ccpcz>/Bbip1<+>	C57BL/6N-Bbip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731257	M	MP:0005013	increased lymphocyte cell number	Bdp1<em1(IMPC)Tcp>/Bdp1<+>	C57BL/6NCrl-Bdp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731257	M	MP:0011874	enlarged urinary bladder	Bdp1<em1(IMPC)Tcp>/Bdp1<+>	C57BL/6NCrl-Bdp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731257	M	MP:0000222	decreased neutrophil cell number	Bdp1<em1(IMPC)Tcp>/Bdp1<+>	C57BL/6NCrl-Bdp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731257	F	MP:0000689	abnormal spleen morphology	Bdp1<em1(IMPC)Tcp>/Bdp1<+>	C57BL/6NCrl-Bdp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731259	M	MP:0002607	decreased basophil cell number	Blnk<em1(IMPC)H>/Blnk<em1(IMPC)H>	C57BL/6N-Blnk<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731259	M	MP:0000221	decreased leukocyte cell number	Blnk<em1(IMPC)H>/Blnk<em1(IMPC)H>	C57BL/6N-Blnk<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731261	F	MP:0002590	increased mean corpuscular volume	Bmp6<em1(IMPC)Ccpcz>/Bmp6<em1(IMPC)Ccpcz>	C57BL/6N-Bmp6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731261	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Bmp6<em1(IMPC)Ccpcz>/Bmp6<em1(IMPC)Ccpcz>	C57BL/6N-Bmp6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731261	M	MP:0001402	decreased locomotor activity	Bmp6<em1(IMPC)Ccpcz>/Bmp6<em1(IMPC)Ccpcz>	C57BL/6N-Bmp6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731261	F	MP:0002060	abnormal skin morphology	Bmp6<em1(IMPC)Ccpcz>/Bmp6<em1(IMPC)Ccpcz>	C57BL/6N-Bmp6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731261	F	MP:0002152	abnormal brain morphology	Bmp6<em1(IMPC)Ccpcz>/Bmp6<em1(IMPC)Ccpcz>	C57BL/6N-Bmp6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731261	M	MP:0005333	decreased heart rate	Bmp6<em1(IMPC)Ccpcz>/Bmp6<em1(IMPC)Ccpcz>	C57BL/6N-Bmp6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731261	F	MP:0005238	increased brain size	Bmp6<em1(IMPC)Ccpcz>/Bmp6<em1(IMPC)Ccpcz>	C57BL/6N-Bmp6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731261	M	MP:0000613	abnormal salivary gland morphology	Bmp6<em1(IMPC)Ccpcz>/Bmp6<em1(IMPC)Ccpcz>	C57BL/6N-Bmp6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731261	M	MP:0005564	increased hemoglobin content	Bmp6<em1(IMPC)Ccpcz>/Bmp6<em1(IMPC)Ccpcz>	C57BL/6N-Bmp6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731261	M	MP:0005343	increased circulating aspartate transaminase level	Bmp6<em1(IMPC)Ccpcz>/Bmp6<em1(IMPC)Ccpcz>	C57BL/6N-Bmp6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731264	M	MP:0001146	abnormal testis morphology	Camk4<em1(IMPC)Ccpcz>/Camk4<em1(IMPC)Ccpcz>	C57BL/6N-Camk4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731264	F	MP:0000703	abnormal thymus morphology	Camk4<em1(IMPC)Ccpcz>/Camk4<em1(IMPC)Ccpcz>	C57BL/6N-Camk4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731264	M	MP:0000689	abnormal spleen morphology	Camk4<em1(IMPC)Ccpcz>/Camk4<em1(IMPC)Ccpcz>	C57BL/6N-Camk4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731264	M	MP:0000274	enlarged heart	Camk4<em1(IMPC)Ccpcz>/Camk4<em1(IMPC)Ccpcz>	C57BL/6N-Camk4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731264	M	MP:0000266	abnormal heart morphology	Camk4<em1(IMPC)Ccpcz>/Camk4<em1(IMPC)Ccpcz>	C57BL/6N-Camk4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731264	M	MP:0001148	enlarged testis	Camk4<em1(IMPC)Ccpcz>/Camk4<em1(IMPC)Ccpcz>	C57BL/6N-Camk4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731264	F	MP:0000709	enlarged thymus	Camk4<em1(IMPC)Ccpcz>/Camk4<em1(IMPC)Ccpcz>	C57BL/6N-Camk4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731264	M	MP:0000692	small spleen	Camk4<em1(IMPC)Ccpcz>/Camk4<em1(IMPC)Ccpcz>	C57BL/6N-Camk4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731266	M	MP:0000221	decreased leukocyte cell number	Ccdc166<em1(IMPC)J>/Ccdc166<em1(IMPC)J>	C57BL/6NJ-Ccdc166<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731267	F	MP:0001926	female infertility	Ccdc180<tm1b(KOMP)Wtsi>/Ccdc180<tm1b(KOMP)Wtsi>	C57BL/6N-Ccdc180<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6731267	M	MP:0001925	male infertility	Ccdc180<tm1b(KOMP)Wtsi>/Ccdc180<tm1b(KOMP)Wtsi>	C57BL/6N-Ccdc180<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6731268	M	MP:0001925	male infertility	Ccdc34<em1(IMPC)J>/Ccdc34<em1(IMPC)J>	C57BL/6NJ-Ccdc34<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731269	F	MP:0005567	decreased circulating total protein level	Ccl3<em1(IMPC)H>/Ccl3<em1(IMPC)H>	C57BL/6N-Ccl3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731269	F	MP:0005419	decreased circulating serum albumin level	Ccl3<em1(IMPC)H>/Ccl3<em1(IMPC)H>	C57BL/6N-Ccl3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731270	F	MP:0005293	impaired glucose tolerance	Ccr9<em1(IMPC)H>/Ccr9<em1(IMPC)H>	C57BL/6N-Ccr9<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731275	M	MP:0006203	eye hemorrhage	Cdh26<tm1.1(KOMP)Vlcg>/Cdh26<tm1.1(KOMP)Vlcg>	C57BL/6N-Cdh26<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6731276	M	MP:0000218	increased leukocyte cell number	Cep68<em1(IMPC)J>/Cep68<em1(IMPC)J>	C57BL/6NJ-Cep68<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731276	M	MP:0001925	male infertility	Cep68<em1(IMPC)J>/Cep68<em1(IMPC)J>	C57BL/6NJ-Cep68<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731276	F	MP:0002833	increased heart weight	Cep68<em1(IMPC)J>/Cep68<em1(IMPC)J>	C57BL/6NJ-Cep68<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731277	F	MP:0011999	abnormal tail length	Chd1l<em1(IMPC)Bay>/Chd1l<em1(IMPC)Bay>	C57BL/6N-Chd1l<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731278	F	MP:0001402	decreased locomotor activity	Cherp<em1(IMPC)J>/Cherp<+>	C57BL/6NJ-Cherp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731279	F	MP:0010052	increased grip strength	Chrnb4<em1(IMPC)H>/Chrnb4<em1(IMPC)H>	C57BL/6N-Chrnb4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731281	M	MP:0001925	male infertility	Cldn11<em1(IMPC)H>/Cldn11<em1(IMPC)H>	C57BL/6N-Cldn11<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731282	F	MP:0002599	increased mean platelet volume	Cnga2<em1(IMPC)H>/Cnga2<em1(IMPC)H>	C57BL/6N-Cnga2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731286	M	MP:0005293	impaired glucose tolerance	Cpd<em1(IMPC)J>/Cpd<+>	C57BL/6NJ-Cpd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731286	M	MP:0005343	increased circulating aspartate transaminase level	Cpd<em1(IMPC)J>/Cpd<+>	C57BL/6NJ-Cpd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731286	M	MP:0005553	increased circulating creatinine level	Cpd<em1(IMPC)J>/Cpd<+>	C57BL/6NJ-Cpd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731286	F	MP:0005278	abnormal cholesterol homeostasis	Cpd<em1(IMPC)J>/Cpd<+>	C57BL/6NJ-Cpd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731290	M	MP:0000691	enlarged spleen	Cyp2f2<em1(IMPC)H>/Cyp2f2<em1(IMPC)H>	C57BL/6N-Cyp2f2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731293	F	MP:0005568	increased circulating total protein level	Dcun1d5<em1(IMPC)H>/Dcun1d5<em1(IMPC)H>	C57BL/6N-Dcun1d5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731293	F	MP:0001392	abnormal locomotor behavior	Dcun1d5<em1(IMPC)H>/Dcun1d5<em1(IMPC)H>	C57BL/6N-Dcun1d5<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731296	F	MP:0001257	increased body length	Dis3l2<em1(IMPC)Bay>/Dis3l2<+>	C57BL/6N-Dis3l2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731297	M	MP:0001914	hemorrhage	Dis3l2<em1(IMPC)Bay>/Dis3l2<em1(IMPC)Bay>	C57BL/6N-Dis3l2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731298	M	MP:0002591	decreased mean corpuscular volume	Dmd<em1(IMPC)Hmgu>/Y	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731298	M	MP:0002941	increased circulating alanine transaminase level	Dmd<em1(IMPC)Hmgu>/Y	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731298	M	MP:0003795	abnormal bone structure	Dmd<em1(IMPC)Hmgu>/Y	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731298	M	MP:0005343	increased circulating aspartate transaminase level	Dmd<em1(IMPC)Hmgu>/Y	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731298	M	MP:0003960	increased lean body mass	Dmd<em1(IMPC)Hmgu>/Y	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731298	M	MP:0010025	decreased total body fat amount	Dmd<em1(IMPC)Hmgu>/Y	C57BL/6N-Dmd<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731299	M	MP:0003385	abnormal body wall morphology	Dnaaf3<em1(IMPC)J>/Dnaaf3<em1(IMPC)J>	C57BL/6NJ-Dnaaf3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731300	F	MP:0001364	decreased anxiety-related response	Dnajc12<em1(IMPC)Bay>/Dnajc12<+>	C57BL/6N-Dnajc12<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731301	F	MP:0011110	preweaning lethality, incomplete penetrance	Dnajc12<em1(IMPC)Bay>/Dnajc12<em1(IMPC)Bay>	C57BL/6N-Dnajc12<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731303	M	MP:0002797	increased thigmotaxis	Dpp8<em1(IMPC)J>/Dpp8<em1(IMPC)J>	C57BL/6NJ-Dpp8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731303	M	MP:0002590	increased mean corpuscular volume	Dpp8<em1(IMPC)J>/Dpp8<em1(IMPC)J>	C57BL/6NJ-Dpp8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731303	F	MP:0003961	decreased lean body mass	Dpp8<em1(IMPC)J>/Dpp8<em1(IMPC)J>	C57BL/6NJ-Dpp8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731303	M	MP:0005333	decreased heart rate	Dpp8<em1(IMPC)J>/Dpp8<em1(IMPC)J>	C57BL/6NJ-Dpp8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731303	M	MP:0005561	increased mean corpuscular hemoglobin	Dpp8<em1(IMPC)J>/Dpp8<em1(IMPC)J>	C57BL/6NJ-Dpp8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731303	M	MP:0005293	impaired glucose tolerance	Dpp8<em1(IMPC)J>/Dpp8<em1(IMPC)J>	C57BL/6NJ-Dpp8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731303	F	MP:0003795	abnormal bone structure	Dpp8<em1(IMPC)J>/Dpp8<em1(IMPC)J>	C57BL/6NJ-Dpp8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731303	F	MP:0000063	decreased bone mineral density	Dpp8<em1(IMPC)J>/Dpp8<em1(IMPC)J>	C57BL/6NJ-Dpp8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731303	M	MP:0002757	decreased vertical activity	Dpp8<em1(IMPC)J>/Dpp8<em1(IMPC)J>	C57BL/6NJ-Dpp8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731303	M	MP:0010506	prolonged RR interval	Dpp8<em1(IMPC)J>/Dpp8<em1(IMPC)J>	C57BL/6NJ-Dpp8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731303	M	MP:0000195	decreased circulating calcium level	Dpp8<em1(IMPC)J>/Dpp8<em1(IMPC)J>	C57BL/6NJ-Dpp8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731304	F	MP:0001399	hyperactivity	Dtx3l<em1(IMPC)H>/Dtx3l<em1(IMPC)H>	C57BL/6N-Dtx3l<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731304	F	MP:0002968	increased circulating alkaline phosphatase level	Dtx3l<em1(IMPC)H>/Dtx3l<em1(IMPC)H>	C57BL/6N-Dtx3l<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731304	F	MP:0005419	decreased circulating serum albumin level	Dtx3l<em1(IMPC)H>/Dtx3l<em1(IMPC)H>	C57BL/6N-Dtx3l<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731304	F	MP:0005561	increased mean corpuscular hemoglobin	Dtx3l<em1(IMPC)H>/Dtx3l<em1(IMPC)H>	C57BL/6N-Dtx3l<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731304	F	MP:0002590	increased mean corpuscular volume	Dtx3l<em1(IMPC)H>/Dtx3l<em1(IMPC)H>	C57BL/6N-Dtx3l<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731305	F	MP:0002574	increased vertical activity	Dzip1l<em1(IMPC)J>/Dzip1l<+>	C57BL/6NJ-Dzip1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731305	F	MP:0001399	hyperactivity	Dzip1l<em1(IMPC)J>/Dzip1l<+>	C57BL/6NJ-Dzip1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731306	F	MP:0001566	increased circulating phosphate level	Eepd1<em1(IMPC)J>/Eepd1<em1(IMPC)J>	C57BL/6NJ-Eepd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731307	F	MP:0009142	decreased prepulse inhibition	Eif2s1<em1(IMPC)Mbp>/Eif2s1<+>	C57BL/6N-Eif2s1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731307	M	MP:0000689	abnormal spleen morphology	Eif2s1<em1(IMPC)Mbp>/Eif2s1<+>	C57BL/6N-Eif2s1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731307	M	MP:0000691	enlarged spleen	Eif2s1<em1(IMPC)Mbp>/Eif2s1<+>	C57BL/6N-Eif2s1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731308	M	MP:0002941	increased circulating alanine transaminase level	Elp6<em1(IMPC)J>/Elp6<+>	C57BL/6NJ-Elp6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731308	M	MP:0005343	increased circulating aspartate transaminase level	Elp6<em1(IMPC)J>/Elp6<+>	C57BL/6NJ-Elp6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731311	F	MP:0011110	preweaning lethality, incomplete penetrance	Eri2<em1(IMPC)Bay>/Eri2<em1(IMPC)Bay>	C57BL/6N-Eri2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731312	M	MP:0010392	prolonged QRS complex duration	Eva1a<em1(IMPC)J>/Eva1a<em1(IMPC)J>	C57BL/6NJ-Eva1a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731313	F	MP:0000702	enlarged lymph nodes	Fabp2<em1(IMPC)Hmgu>/Fabp2<em1(IMPC)Hmgu>	C57BL/6N-Fabp2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731313	M	MP:0005567	decreased circulating total protein level	Fabp2<em1(IMPC)Hmgu>/Fabp2<em1(IMPC)Hmgu>	C57BL/6N-Fabp2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731314	F	MP:0000691	enlarged spleen	Fah<em1(IMPC)Mbp>/Fah<+>	C57BL/6N-Fah<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731314	M	MP:0003068	enlarged kidney	Fah<em1(IMPC)Mbp>/Fah<+>	C57BL/6N-Fah<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731314	M	MP:0000266	abnormal heart morphology	Fah<em1(IMPC)Mbp>/Fah<+>	C57BL/6N-Fah<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731314	M	MP:0000601	small liver	Fah<em1(IMPC)Mbp>/Fah<+>	C57BL/6N-Fah<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731314	F	MP:0000689	abnormal spleen morphology	Fah<em1(IMPC)Mbp>/Fah<+>	C57BL/6N-Fah<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731314	M	MP:0001146	abnormal testis morphology	Fah<em1(IMPC)Mbp>/Fah<+>	C57BL/6N-Fah<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731314	M	MP:0000274	enlarged heart	Fah<em1(IMPC)Mbp>/Fah<+>	C57BL/6N-Fah<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731314	M	MP:0001148	enlarged testis	Fah<em1(IMPC)Mbp>/Fah<+>	C57BL/6N-Fah<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731314	M	MP:0002060	abnormal skin morphology	Fah<em1(IMPC)Mbp>/Fah<+>	C57BL/6N-Fah<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731314	F	MP:0010097	abnormal retina blood vessel morphology	Fah<em1(IMPC)Mbp>/Fah<+>	C57BL/6N-Fah<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731314	F	MP:0002989	small kidney	Fah<em1(IMPC)Mbp>/Fah<+>	C57BL/6N-Fah<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731314	M	MP:0000598	abnormal liver morphology	Fah<em1(IMPC)Mbp>/Fah<+>	C57BL/6N-Fah<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731315	F	MP:0001120	abnormal uterus morphology	Fam185a<em1(IMPC)Ccpcz>/Fam185a<em1(IMPC)Ccpcz>	C57BL/6N-Fam185a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731315	M	MP:0000266	abnormal heart morphology	Fam185a<em1(IMPC)Ccpcz>/Fam185a<em1(IMPC)Ccpcz>	C57BL/6N-Fam185a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731315	F	MP:0000709	enlarged thymus	Fam185a<em1(IMPC)Ccpcz>/Fam185a<em1(IMPC)Ccpcz>	C57BL/6N-Fam185a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731315	M	MP:0000689	abnormal spleen morphology	Fam185a<em1(IMPC)Ccpcz>/Fam185a<em1(IMPC)Ccpcz>	C57BL/6N-Fam185a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731315	F	MP:0002060	abnormal skin morphology	Fam185a<em1(IMPC)Ccpcz>/Fam185a<em1(IMPC)Ccpcz>	C57BL/6N-Fam185a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731315	M	MP:0001489	decreased startle reflex	Fam185a<em1(IMPC)Ccpcz>/Fam185a<em1(IMPC)Ccpcz>	C57BL/6N-Fam185a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731315	F	MP:0000703	abnormal thymus morphology	Fam185a<em1(IMPC)Ccpcz>/Fam185a<em1(IMPC)Ccpcz>	C57BL/6N-Fam185a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731315	F	MP:0009709	hydrometra	Fam185a<em1(IMPC)Ccpcz>/Fam185a<em1(IMPC)Ccpcz>	C57BL/6N-Fam185a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731315	M	MP:0005554	decreased circulating creatinine level	Fam185a<em1(IMPC)Ccpcz>/Fam185a<em1(IMPC)Ccpcz>	C57BL/6N-Fam185a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731315	M	MP:0000274	enlarged heart	Fam185a<em1(IMPC)Ccpcz>/Fam185a<em1(IMPC)Ccpcz>	C57BL/6N-Fam185a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731315	M	MP:0011047	increased lung tissue damping	Fam185a<em1(IMPC)Ccpcz>/Fam185a<em1(IMPC)Ccpcz>	C57BL/6N-Fam185a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731317	M	MP:0001146	abnormal testis morphology	Fam221a<em1(IMPC)Ccpcz>/Fam221a<em1(IMPC)Ccpcz>	C57BL/6N-Fam221a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731317	M	MP:0010935	increased airway resistance	Fam221a<em1(IMPC)Ccpcz>/Fam221a<em1(IMPC)Ccpcz>	C57BL/6N-Fam221a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731317	F	MP:0005559	increased circulating glucose level	Fam221a<em1(IMPC)Ccpcz>/Fam221a<em1(IMPC)Ccpcz>	C57BL/6N-Fam221a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731317	M	MP:0013436	increased CD8-positive, naive alpha-beta T cell number	Fam221a<em1(IMPC)Ccpcz>/Fam221a<em1(IMPC)Ccpcz>	C57BL/6N-Fam221a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731317	M	MP:0000702	enlarged lymph nodes	Fam221a<em1(IMPC)Ccpcz>/Fam221a<em1(IMPC)Ccpcz>	C57BL/6N-Fam221a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731317	M	MP:0002092	abnormal eye morphology	Fam221a<em1(IMPC)Ccpcz>/Fam221a<em1(IMPC)Ccpcz>	C57BL/6N-Fam221a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731317	M	MP:0000219	increased neutrophil cell number	Fam221a<em1(IMPC)Ccpcz>/Fam221a<em1(IMPC)Ccpcz>	C57BL/6N-Fam221a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731317	M	MP:0002339	abnormal lymph node morphology	Fam221a<em1(IMPC)Ccpcz>/Fam221a<em1(IMPC)Ccpcz>	C57BL/6N-Fam221a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731317	M	MP:0000266	abnormal heart morphology	Fam221a<em1(IMPC)Ccpcz>/Fam221a<em1(IMPC)Ccpcz>	C57BL/6N-Fam221a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731317	M	MP:0000274	enlarged heart	Fam221a<em1(IMPC)Ccpcz>/Fam221a<em1(IMPC)Ccpcz>	C57BL/6N-Fam221a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731317	M	MP:0001147	small testis	Fam221a<em1(IMPC)Ccpcz>/Fam221a<em1(IMPC)Ccpcz>	C57BL/6N-Fam221a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731317	F	MP:0005568	increased circulating total protein level	Fam221a<em1(IMPC)Ccpcz>/Fam221a<em1(IMPC)Ccpcz>	C57BL/6N-Fam221a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731318	F	MP:0005568	increased circulating total protein level	Fam53a<em1(IMPC)Ccpcz>/Fam53a<em1(IMPC)Ccpcz>	C57BL/6N-Fam53a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731318	F	MP:0001297	microphthalmia	Fam53a<em1(IMPC)Ccpcz>/Fam53a<em1(IMPC)Ccpcz>	C57BL/6N-Fam53a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731318	M	MP:0000689	abnormal spleen morphology	Fam53a<em1(IMPC)Ccpcz>/Fam53a<em1(IMPC)Ccpcz>	C57BL/6N-Fam53a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731318	M	MP:0002997	enlarged seminal vesicle	Fam53a<em1(IMPC)Ccpcz>/Fam53a<em1(IMPC)Ccpcz>	C57BL/6N-Fam53a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731318	F	MP:0004174	abnormal spine curvature	Fam53a<em1(IMPC)Ccpcz>/Fam53a<em1(IMPC)Ccpcz>	C57BL/6N-Fam53a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731318	M	MP:0002059	abnormal seminal vesicle morphology	Fam53a<em1(IMPC)Ccpcz>/Fam53a<em1(IMPC)Ccpcz>	C57BL/6N-Fam53a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731318	M	MP:0000274	enlarged heart	Fam53a<em1(IMPC)Ccpcz>/Fam53a<em1(IMPC)Ccpcz>	C57BL/6N-Fam53a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731318	F	MP:0002060	abnormal skin morphology	Fam53a<em1(IMPC)Ccpcz>/Fam53a<em1(IMPC)Ccpcz>	C57BL/6N-Fam53a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731318	F	MP:0002092	abnormal eye morphology	Fam53a<em1(IMPC)Ccpcz>/Fam53a<em1(IMPC)Ccpcz>	C57BL/6N-Fam53a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731318	M	MP:0000266	abnormal heart morphology	Fam53a<em1(IMPC)Ccpcz>/Fam53a<em1(IMPC)Ccpcz>	C57BL/6N-Fam53a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731319	M	MP:0001147	small testis	Garin2<em1(IMPC)Ccpcz>/Garin2<em1(IMPC)Ccpcz>	C57BL/6N-Garin2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731319	F	MP:0000689	abnormal spleen morphology	Garin2<em1(IMPC)Ccpcz>/Garin2<em1(IMPC)Ccpcz>	C57BL/6N-Garin2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731319	F	MP:0000709	enlarged thymus	Garin2<em1(IMPC)Ccpcz>/Garin2<em1(IMPC)Ccpcz>	C57BL/6N-Garin2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731319	F	MP:0000703	abnormal thymus morphology	Garin2<em1(IMPC)Ccpcz>/Garin2<em1(IMPC)Ccpcz>	C57BL/6N-Garin2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731319	F	MP:0000691	enlarged spleen	Garin2<em1(IMPC)Ccpcz>/Garin2<em1(IMPC)Ccpcz>	C57BL/6N-Garin2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731319	M	MP:0001146	abnormal testis morphology	Garin2<em1(IMPC)Ccpcz>/Garin2<em1(IMPC)Ccpcz>	C57BL/6N-Garin2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731320	M	MP:0001157	small seminal vesicle	Garin1a<em1(IMPC)Ccpcz>/Garin1a<em1(IMPC)Ccpcz>	C57BL/6N-Garin1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731320	F	MP:0000691	enlarged spleen	Garin1a<em1(IMPC)Ccpcz>/Garin1a<em1(IMPC)Ccpcz>	C57BL/6N-Garin1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731320	M	MP:0001262	decreased body weight	Garin1a<em1(IMPC)Ccpcz>/Garin1a<em1(IMPC)Ccpcz>	C57BL/6N-Garin1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731320	M	MP:0002135	abnormal kidney morphology	Garin1a<em1(IMPC)Ccpcz>/Garin1a<em1(IMPC)Ccpcz>	C57BL/6N-Garin1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731320	M	MP:0002059	abnormal seminal vesicle morphology	Garin1a<em1(IMPC)Ccpcz>/Garin1a<em1(IMPC)Ccpcz>	C57BL/6N-Garin1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731320	F	MP:0001120	abnormal uterus morphology	Garin1a<em1(IMPC)Ccpcz>/Garin1a<em1(IMPC)Ccpcz>	C57BL/6N-Garin1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731320	F	MP:0009709	hydrometra	Garin1a<em1(IMPC)Ccpcz>/Garin1a<em1(IMPC)Ccpcz>	C57BL/6N-Garin1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731321	M	MP:0010024	increased total body fat amount	Fam81b<em1(IMPC)J>/Fam81b<em1(IMPC)J>	C57BL/6NJ-Fam81b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731321	M	MP:0003961	decreased lean body mass	Fam81b<em1(IMPC)J>/Fam81b<em1(IMPC)J>	C57BL/6NJ-Fam81b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731322	M	MP:0000274	enlarged heart	Fam83d<em1(IMPC)Ccpcz>/Fam83d<em1(IMPC)Ccpcz>	C57BL/6N-Fam83d<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731322	M	MP:0013279	increased fasting circulating glucose level	Fam83d<em1(IMPC)Ccpcz>/Fam83d<em1(IMPC)Ccpcz>	C57BL/6N-Fam83d<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731322	F	MP:0009142	decreased prepulse inhibition	Fam83d<em1(IMPC)Ccpcz>/Fam83d<em1(IMPC)Ccpcz>	C57BL/6N-Fam83d<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731322	M	MP:0000709	enlarged thymus	Fam83d<em1(IMPC)Ccpcz>/Fam83d<em1(IMPC)Ccpcz>	C57BL/6N-Fam83d<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731322	M	MP:0001148	enlarged testis	Fam83d<em1(IMPC)Ccpcz>/Fam83d<em1(IMPC)Ccpcz>	C57BL/6N-Fam83d<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731322	M	MP:0001489	decreased startle reflex	Fam83d<em1(IMPC)Ccpcz>/Fam83d<em1(IMPC)Ccpcz>	C57BL/6N-Fam83d<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731322	M	MP:0000266	abnormal heart morphology	Fam83d<em1(IMPC)Ccpcz>/Fam83d<em1(IMPC)Ccpcz>	C57BL/6N-Fam83d<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731322	M	MP:0002135	abnormal kidney morphology	Fam83d<em1(IMPC)Ccpcz>/Fam83d<em1(IMPC)Ccpcz>	C57BL/6N-Fam83d<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731322	M	MP:0001146	abnormal testis morphology	Fam83d<em1(IMPC)Ccpcz>/Fam83d<em1(IMPC)Ccpcz>	C57BL/6N-Fam83d<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731322	M	MP:0000703	abnormal thymus morphology	Fam83d<em1(IMPC)Ccpcz>/Fam83d<em1(IMPC)Ccpcz>	C57BL/6N-Fam83d<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731322	M	MP:0005343	increased circulating aspartate transaminase level	Fam83d<em1(IMPC)Ccpcz>/Fam83d<em1(IMPC)Ccpcz>	C57BL/6N-Fam83d<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731323	F	MP:0003604	single kidney	Fbxw15<em1(IMPC)Ccpcz>/Fbxw15<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw15<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731323	F	MP:0001175	abnormal lung morphology	Fbxw15<em1(IMPC)Ccpcz>/Fbxw15<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw15<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731323	M	MP:0001566	increased circulating phosphate level	Fbxw15<em1(IMPC)Ccpcz>/Fbxw15<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw15<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731323	M	MP:0005270	abnormal zygomatic bone morphology	Fbxw15<em1(IMPC)Ccpcz>/Fbxw15<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw15<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	M	MP:0000692	small spleen	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	M	MP:0000691	enlarged spleen	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	M	MP:0001157	small seminal vesicle	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	F	MP:0003019	increased circulating chloride level	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	F	MP:0002100	abnormal tooth morphology	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	M	MP:0002060	abnormal skin morphology	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	M	MP:0000266	abnormal heart morphology	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	M	MP:0000689	abnormal spleen morphology	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	M	MP:0001891	hydrocephaly	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	M	MP:0001146	abnormal testis morphology	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	M	MP:0002152	abnormal brain morphology	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	M	MP:0001147	small testis	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	M	MP:0002059	abnormal seminal vesicle morphology	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731324	M	MP:0000274	enlarged heart	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<+>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731325	M	MP:0001147	small testis	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731325	M	MP:0002100	abnormal tooth morphology	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731325	M	MP:0001146	abnormal testis morphology	Fbxw18<em1(IMPC)Ccpcz>/Fbxw18<em1(IMPC)Ccpcz>	C57BL/6N-Fbxw18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731326	M	MP:0001304	cataract	Fgfr1op2<em1(IMPC)Mbp>/Fgfr1op2<+>	C57BL/6N-Fgfr1op2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731326	F	MP:0002060	abnormal skin morphology	Fgfr1op2<em1(IMPC)Mbp>/Fgfr1op2<+>	C57BL/6N-Fgfr1op2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731326	M	MP:0001325	abnormal retina morphology	Fgfr1op2<em1(IMPC)Mbp>/Fgfr1op2<+>	C57BL/6N-Fgfr1op2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731327	F	MP:0010507	shortened RR interval	Fhod1<em1(IMPC)J>/Fhod1<em1(IMPC)J>	C57BL/6NJ-Fhod1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731327	F	MP:0002626	increased heart rate	Fhod1<em1(IMPC)J>/Fhod1<em1(IMPC)J>	C57BL/6NJ-Fhod1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731327	M	MP:0002833	increased heart weight	Fhod1<em1(IMPC)J>/Fhod1<em1(IMPC)J>	C57BL/6NJ-Fhod1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731328	F	MP:0000774	decreased brain size	Fmo5<em1(IMPC)Mbp>/Fmo5<em1(IMPC)Mbp>	C57BL/6N-Fmo5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731328	F	MP:0002135	abnormal kidney morphology	Fmo5<em1(IMPC)Mbp>/Fmo5<em1(IMPC)Mbp>	C57BL/6N-Fmo5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731328	F	MP:0002152	abnormal brain morphology	Fmo5<em1(IMPC)Mbp>/Fmo5<em1(IMPC)Mbp>	C57BL/6N-Fmo5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731328	F	MP:0000689	abnormal spleen morphology	Fmo5<em1(IMPC)Mbp>/Fmo5<em1(IMPC)Mbp>	C57BL/6N-Fmo5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731328	F	MP:0000601	small liver	Fmo5<em1(IMPC)Mbp>/Fmo5<em1(IMPC)Mbp>	C57BL/6N-Fmo5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731328	F	MP:0002060	abnormal skin morphology	Fmo5<em1(IMPC)Mbp>/Fmo5<em1(IMPC)Mbp>	C57BL/6N-Fmo5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731328	F	MP:0000691	enlarged spleen	Fmo5<em1(IMPC)Mbp>/Fmo5<em1(IMPC)Mbp>	C57BL/6N-Fmo5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731328	F	MP:0003068	enlarged kidney	Fmo5<em1(IMPC)Mbp>/Fmo5<em1(IMPC)Mbp>	C57BL/6N-Fmo5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731328	F	MP:0000598	abnormal liver morphology	Fmo5<em1(IMPC)Mbp>/Fmo5<em1(IMPC)Mbp>	C57BL/6N-Fmo5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731329	M	MP:0003179	thrombocytopenia	Fsbp<em1(IMPC)J>/Fsbp<em1(IMPC)J>	C57BL/6NJ-Fsbp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731330	M	MP:0010506	prolonged RR interval	Gabre<em1(IMPC)H>/Y	C57BL/6N-Gabre<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731333	F	MP:0005011	increased eosinophil cell number	Galr1<em1(IMPC)H>/Galr1<em1(IMPC)H>	C57BL/6N-Galr1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731333	F	MP:0000691	enlarged spleen	Galr1<em1(IMPC)H>/Galr1<em1(IMPC)H>	C57BL/6N-Galr1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731333	F	MP:0005016	decreased lymphocyte cell number	Galr1<em1(IMPC)H>/Galr1<em1(IMPC)H>	C57BL/6N-Galr1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731335	F	MP:0005419	decreased circulating serum albumin level	Gje1<em1(IMPC)H>/Gje1<em1(IMPC)H>	C57BL/6NTac-Gje1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731336	F	MP:0002824	abnormal chorioallantoic fusion	Glmn<em1(IMPC)Bay>/Glmn<em1(IMPC)Bay>	C57BL/6N-Glmn<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731337	M	MP:0000195	decreased circulating calcium level	Gm28729<em1(IMPC)J>/Gm28729<em1(IMPC)J>	C57BL/6NJ-Gm28729<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731337	M	MP:0000221	decreased leukocyte cell number	Gm28729<em1(IMPC)J>/Gm28729<em1(IMPC)J>	C57BL/6NJ-Gm28729<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731338	F	MP:0009142	decreased prepulse inhibition	Gne<em1(IMPC)Mbp>/Gne<+>	C57BL/6N-Gne<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731338	F	MP:0002699	abnormal vitreous body morphology	Gne<em1(IMPC)Mbp>/Gne<+>	C57BL/6N-Gne<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731338	M	MP:0001289	persistence of hyaloid vascular system	Gne<em1(IMPC)Mbp>/Gne<+>	C57BL/6N-Gne<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731340	M	MP:0001489	decreased startle reflex	Grxcr1<em1(IMPC)J>/Grxcr1<em1(IMPC)J>	C57BL/6NJ-Grxcr1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731340	M	MP:0002102	abnormal ear morphology	Grxcr1<em1(IMPC)J>/Grxcr1<em1(IMPC)J>	C57BL/6NJ-Grxcr1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731340	F	MP:0001486	abnormal startle reflex	Grxcr1<em1(IMPC)J>/Grxcr1<em1(IMPC)J>	C57BL/6NJ-Grxcr1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731340	F	MP:0009142	decreased prepulse inhibition	Grxcr1<em1(IMPC)J>/Grxcr1<em1(IMPC)J>	C57BL/6NJ-Grxcr1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731340	M	MP:0005178	increased circulating cholesterol level	Grxcr1<em1(IMPC)J>/Grxcr1<em1(IMPC)J>	C57BL/6NJ-Grxcr1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731341	M	MP:0010392	prolonged QRS complex duration	Gtf2h3<em1(IMPC)J>/Gtf2h3<+>	C57BL/6NJ-Gtf2h3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731343	M	MP:0011100	preweaning lethality, complete penetrance	Gys1<em1(IMPC)Bay>/Gys1<em1(IMPC)Bay>	C57BL/6N-Gys1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731346	F	MP:0002968	increased circulating alkaline phosphatase level	Hdac7<tm1b(EUCOMM)Hmgu>/Hdac7<+>	C57BL/6N-Hdac7<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:6731346	F	MP:0005278	abnormal cholesterol homeostasis	Hdac7<tm1b(EUCOMM)Hmgu>/Hdac7<+>	C57BL/6N-Hdac7<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:6731347	M	MP:0010024	increased total body fat amount	Hsf5<em1(IMPC)J>/Hsf5<em1(IMPC)J>	C57BL/6NJ-Hsf5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731347	M	MP:0005333	decreased heart rate	Hsf5<em1(IMPC)J>/Hsf5<em1(IMPC)J>	C57BL/6NJ-Hsf5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731347	M	MP:0001925	male infertility	Hsf5<em1(IMPC)J>/Hsf5<em1(IMPC)J>	C57BL/6NJ-Hsf5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731347	M	MP:0003961	decreased lean body mass	Hsf5<em1(IMPC)J>/Hsf5<em1(IMPC)J>	C57BL/6NJ-Hsf5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731348	M	MP:0001925	male infertility	Hsfy2<em1(IMPC)J>/Hsfy2<em1(IMPC)J>	C57BL/6NJ-Hsfy2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731349	M	MP:0001488	increased startle reflex	Iffo2<em1(IMPC)J>/Iffo2<em1(IMPC)J>	C57BL/6NJ-Iffo2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731350	M	MP:0001402	decreased locomotor activity	Igf2bp1<em1(IMPC)J>/Igf2bp1<+>	C57BL/6NJ-Igf2bp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731351	F	MP:0005293	impaired glucose tolerance	Il12b<em1(IMPC)H>/Il12b<em1(IMPC)H>	C57BL/6NTac-Il12b<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731353	F	MP:0009142	decreased prepulse inhibition	Immp2l<em1(IMPC)Bay>/Immp2l<em1(IMPC)Bay>	C57BL/6N-Immp2l<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731353	F	MP:0001258	decreased body length	Immp2l<em1(IMPC)Bay>/Immp2l<em1(IMPC)Bay>	C57BL/6N-Immp2l<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731354	M	MP:0002574	increased vertical activity	Ino80c<em1(IMPC)J>/Ino80c<+>	C57BL/6NJ-Ino80c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731354	F	MP:0006203	eye hemorrhage	Ino80c<em1(IMPC)J>/Ino80c<+>	C57BL/6NJ-Ino80c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731356	M	MP:0005293	impaired glucose tolerance	Iqcf1<em1(IMPC)J>/Iqcf1<em1(IMPC)J>	C57BL/6NJ-Iqcf1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731357	M	MP:0001148	enlarged testis	Kansl1l<tm1b(EUCOMM)Wtsi>/Kansl1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Kansl1l<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6731357	M	MP:0001147	small testis	Kansl1l<tm1b(EUCOMM)Wtsi>/Kansl1l<tm1b(EUCOMM)Wtsi>	C57BL/6N-Kansl1l<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6731359	M	MP:0011874	enlarged urinary bladder	Kctd3<em1(IMPC)Tcp>/Kctd3<+>	C57BL/6N-Kctd3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731359	M	MP:0002092	abnormal eye morphology	Kctd3<em1(IMPC)Tcp>/Kctd3<+>	C57BL/6N-Kctd3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731359	M	MP:0005562	decreased mean corpuscular hemoglobin	Kctd3<em1(IMPC)Tcp>/Kctd3<+>	C57BL/6N-Kctd3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731360	M	MP:0000195	decreased circulating calcium level	Kctd5<em1(IMPC)J>/Kctd5<+>	C57BL/6NJ-Kctd5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731363	F	MP:0000703	abnormal thymus morphology	Klhl1<em1(IMPC)Ccpcz>/Klhl1<em1(IMPC)Ccpcz>	C57BL/6N-Klhl1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731363	F	MP:0002060	abnormal skin morphology	Klhl1<em1(IMPC)Ccpcz>/Klhl1<em1(IMPC)Ccpcz>	C57BL/6N-Klhl1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731363	M	MP:0004931	enlarged epididymis	Klhl1<em1(IMPC)Ccpcz>/Klhl1<em1(IMPC)Ccpcz>	C57BL/6N-Klhl1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731363	M	MP:0000692	small spleen	Klhl1<em1(IMPC)Ccpcz>/Klhl1<em1(IMPC)Ccpcz>	C57BL/6N-Klhl1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731363	M	MP:0001147	small testis	Klhl1<em1(IMPC)Ccpcz>/Klhl1<em1(IMPC)Ccpcz>	C57BL/6N-Klhl1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731363	M	MP:0001146	abnormal testis morphology	Klhl1<em1(IMPC)Ccpcz>/Klhl1<em1(IMPC)Ccpcz>	C57BL/6N-Klhl1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731363	M	MP:0001262	decreased body weight	Klhl1<em1(IMPC)Ccpcz>/Klhl1<em1(IMPC)Ccpcz>	C57BL/6N-Klhl1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731363	M	MP:0002631	abnormal epididymis morphology	Klhl1<em1(IMPC)Ccpcz>/Klhl1<em1(IMPC)Ccpcz>	C57BL/6N-Klhl1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731363	M	MP:0001415	increased exploration in new environment	Klhl1<em1(IMPC)Ccpcz>/Klhl1<em1(IMPC)Ccpcz>	C57BL/6N-Klhl1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731363	F	MP:0000160	kyphosis	Klhl1<em1(IMPC)Ccpcz>/Klhl1<em1(IMPC)Ccpcz>	C57BL/6N-Klhl1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731363	F	MP:0000709	enlarged thymus	Klhl1<em1(IMPC)Ccpcz>/Klhl1<em1(IMPC)Ccpcz>	C57BL/6N-Klhl1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731363	F	MP:0000691	enlarged spleen	Klhl1<em1(IMPC)Ccpcz>/Klhl1<em1(IMPC)Ccpcz>	C57BL/6N-Klhl1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731364	M	MP:0002092	abnormal eye morphology	Krt72<em1(IMPC)Ccpcz>/Krt72<em1(IMPC)Ccpcz>	C57BL/6N-Krt72<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731364	F	MP:0009709	hydrometra	Krt72<em1(IMPC)Ccpcz>/Krt72<em1(IMPC)Ccpcz>	C57BL/6N-Krt72<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731364	F	MP:0001120	abnormal uterus morphology	Krt72<em1(IMPC)Ccpcz>/Krt72<em1(IMPC)Ccpcz>	C57BL/6N-Krt72<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731364	M	MP:0000538	abnormal urinary bladder morphology	Krt72<em1(IMPC)Ccpcz>/Krt72<em1(IMPC)Ccpcz>	C57BL/6N-Krt72<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731364	M	MP:0001147	small testis	Krt72<em1(IMPC)Ccpcz>/Krt72<em1(IMPC)Ccpcz>	C57BL/6N-Krt72<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731364	M	MP:0004174	abnormal spine curvature	Krt72<em1(IMPC)Ccpcz>/Krt72<em1(IMPC)Ccpcz>	C57BL/6N-Krt72<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731364	M	MP:0000160	kyphosis	Krt72<em1(IMPC)Ccpcz>/Krt72<em1(IMPC)Ccpcz>	C57BL/6N-Krt72<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731364	F	MP:0000689	abnormal spleen morphology	Krt72<em1(IMPC)Ccpcz>/Krt72<em1(IMPC)Ccpcz>	C57BL/6N-Krt72<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731365	M	MP:0002060	abnormal skin morphology	Lamp3<em1(IMPC)Tcp>/Lamp3<em1(IMPC)Tcp>	C57BL/6N-Lamp3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731365	M	MP:0002339	abnormal lymph node morphology	Lamp3<em1(IMPC)Tcp>/Lamp3<em1(IMPC)Tcp>	C57BL/6N-Lamp3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731365	M	MP:0000157	abnormal sternum morphology	Lamp3<em1(IMPC)Tcp>/Lamp3<em1(IMPC)Tcp>	C57BL/6N-Lamp3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731365	M	MP:0002631	abnormal epididymis morphology	Lamp3<em1(IMPC)Tcp>/Lamp3<em1(IMPC)Tcp>	C57BL/6N-Lamp3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0000438	abnormal cranium morphology	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0000219	increased neutrophil cell number	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0001417	decreased exploration in new environment	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0002764	short tibia	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	M	MP:0000550	abnormal forelimb morphology	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0002060	abnormal skin morphology	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0000220	increased monocyte cell number	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	M	MP:0001157	small seminal vesicle	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0002966	decreased circulating alkaline phosphatase level	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0010124	decreased bone mineral content	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	M	MP:0001147	small testis	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0005562	decreased mean corpuscular hemoglobin	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0005016	decreased lymphocyte cell number	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0001258	decreased body length	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0010053	decreased grip strength	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0009142	decreased prepulse inhibition	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0001402	decreased locomotor activity	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0000063	decreased bone mineral density	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	M	MP:0000702	enlarged lymph nodes	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0003795	abnormal bone structure	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	M	MP:0011110	preweaning lethality, incomplete penetrance	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731366	F	MP:0002111	abnormal tail morphology	Lbr<em1(IMPC)Tcp>/Lbr<em1(IMPC)Tcp>	C57BL/6N-Lbr<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731368	F	MP:0005567	decreased circulating total protein level	Lonrf2<em2(IMPC)H>/Lonrf2<em2(IMPC)H>	C57BL/6N-Lonrf2<em2(IMPC)H>/H	N	MGI:5576271
MGI:6731368	M	MP:0000194	increased circulating calcium level	Lonrf2<em2(IMPC)H>/Lonrf2<em2(IMPC)H>	C57BL/6N-Lonrf2<em2(IMPC)H>/H	N	MGI:5576271
MGI:6731368	M	MP:0005553	increased circulating creatinine level	Lonrf2<em2(IMPC)H>/Lonrf2<em2(IMPC)H>	C57BL/6N-Lonrf2<em2(IMPC)H>/H	N	MGI:5576271
MGI:6731368	M	MP:0005565	increased blood urea nitrogen level	Lonrf2<em2(IMPC)H>/Lonrf2<em2(IMPC)H>	C57BL/6N-Lonrf2<em2(IMPC)H>/H	N	MGI:5576271
MGI:6731369	M	MP:0003131	increased erythrocyte cell number	Lpcat2<em1(IMPC)J>/Lpcat2<em1(IMPC)J>	C57BL/6NJ-Lpcat2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731369	M	MP:0010052	increased grip strength	Lpcat2<em1(IMPC)J>/Lpcat2<em1(IMPC)J>	C57BL/6NJ-Lpcat2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731369	M	MP:0002608	increased hematocrit	Lpcat2<em1(IMPC)J>/Lpcat2<em1(IMPC)J>	C57BL/6NJ-Lpcat2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731369	M	MP:0005178	increased circulating cholesterol level	Lpcat2<em1(IMPC)J>/Lpcat2<em1(IMPC)J>	C57BL/6NJ-Lpcat2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731370	M	MP:0010024	increased total body fat amount	Lysmd1<em1(IMPC)J>/Lysmd1<em1(IMPC)J>	C57BL/6NJ-Lysmd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731370	M	MP:0010124	decreased bone mineral content	Lysmd1<em1(IMPC)J>/Lysmd1<em1(IMPC)J>	C57BL/6NJ-Lysmd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731372	F	MP:0010506	prolonged RR interval	Maged1<em1(IMPC)Mbp>/Maged1<em1(IMPC)Mbp>	C57BL/6N-Maged1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731372	F	MP:0020421	increased freezing behavior	Maged1<em1(IMPC)Mbp>/Maged1<em1(IMPC)Mbp>	C57BL/6N-Maged1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731372	F	MP:0005333	decreased heart rate	Maged1<em1(IMPC)Mbp>/Maged1<em1(IMPC)Mbp>	C57BL/6N-Maged1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731372	F	MP:0002757	decreased vertical activity	Maged1<em1(IMPC)Mbp>/Maged1<em1(IMPC)Mbp>	C57BL/6N-Maged1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731372	F	MP:0001402	decreased locomotor activity	Maged1<em1(IMPC)Mbp>/Maged1<em1(IMPC)Mbp>	C57BL/6N-Maged1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731373	F	MP:0011110	preweaning lethality, incomplete penetrance	Man1b1<em1(IMPC)Bay>/Man1b1<em1(IMPC)Bay>	C57BL/6N-Man1b1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731374	F	MP:0002092	abnormal eye morphology	Mapk6<em1(IMPC)Mbp>/Mapk6<+>	C57BL/6N-Mapk6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731374	F	MP:0000774	decreased brain size	Mapk6<em1(IMPC)Mbp>/Mapk6<+>	C57BL/6N-Mapk6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731374	F	MP:0002152	abnormal brain morphology	Mapk6<em1(IMPC)Mbp>/Mapk6<+>	C57BL/6N-Mapk6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731374	F	MP:0001293	anophthalmia	Mapk6<em1(IMPC)Mbp>/Mapk6<+>	C57BL/6N-Mapk6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731374	M	MP:0001304	cataract	Mapk6<em1(IMPC)Mbp>/Mapk6<+>	C57BL/6N-Mapk6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731374	M	MP:0002699	abnormal vitreous body morphology	Mapk6<em1(IMPC)Mbp>/Mapk6<+>	C57BL/6N-Mapk6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731376	F	MP:0000703	abnormal thymus morphology	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	M	MP:0001147	small testis	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	M	MP:0002059	abnormal seminal vesicle morphology	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	M	MP:0000538	abnormal urinary bladder morphology	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	M	MP:0011048	decreased lung tissue damping	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	F	MP:0000598	abnormal liver morphology	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	F	MP:0002060	abnormal skin morphology	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	M	MP:0001146	abnormal testis morphology	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	F	MP:0005293	impaired glucose tolerance	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	M	MP:0013129	abnormal tooth color	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	F	MP:0001297	microphthalmia	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	F	MP:0000601	small liver	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	F	MP:0002092	abnormal eye morphology	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	M	MP:0002100	abnormal tooth morphology	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	F	MP:0000709	enlarged thymus	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731376	M	MP:0011625	cystolithiasis	Meis3<tm1b(EUCOMM)Hmgu>/Meis3<tm1b(EUCOMM)Hmgu>	C57BL/6N-Meis3<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:6731377	F	MP:0010052	increased grip strength	Mettl5<em1(IMPC)Hmgu>/Mettl5<+>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731377	F	MP:0005566	decreased blood urea nitrogen level	Mettl5<em1(IMPC)Hmgu>/Mettl5<+>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0001304	cataract	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0002757	decreased vertical activity	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0000208	decreased hematocrit	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0001322	abnormal iris morphology	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0001399	hyperactivity	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0020870	decreased thigmotaxis	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0010052	increased grip strength	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0002874	decreased hemoglobin content	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0001258	decreased body length	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0001325	abnormal retina morphology	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0004924	abnormal behavior	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0004952	increased spleen weight	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0004222	iris synechia	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	F	MP:0001312	abnormal cornea morphology	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0001303	abnormal lens morphology	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0008259	abnormal optic disk morphology	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0002875	decreased erythrocyte cell number	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0001402	decreased locomotor activity	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731378	M	MP:0001364	decreased anxiety-related response	Mettl5<em1(IMPC)Hmgu>/Mettl5<em1(IMPC)Hmgu>	C57BL/6N-Mettl5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731379	M	MP:0002757	decreased vertical activity	Msantd2<em1(IMPC)J>/Msantd2<em1(IMPC)J>	C57BL/6NJ-Msantd2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731379	M	MP:0001325	abnormal retina morphology	Msantd2<em1(IMPC)J>/Msantd2<em1(IMPC)J>	C57BL/6NJ-Msantd2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731382	M	MP:0000221	decreased leukocyte cell number	Mtx2<em1(IMPC)J>/Mtx2<+>	C57BL/6NJ-Mtx2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731383	F	MP:0011962	increased cornea thickness	Myrf<em1(IMPC)Bay>/Myrf<+>	C57BL/6N-Myrf<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731384	F	MP:0001697	abnormal embryo size	Myrf<em1(IMPC)Bay>/Myrf<em1(IMPC)Bay>	C57BL/6N-Myrf<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731384	F	MP:0001700	abnormal embryo turning	Myrf<em1(IMPC)Bay>/Myrf<em1(IMPC)Bay>	C57BL/6N-Myrf<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731384	F	MP:0003984	embryonic growth retardation	Myrf<em1(IMPC)Bay>/Myrf<em1(IMPC)Bay>	C57BL/6N-Myrf<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731388	F	MP:0000709	enlarged thymus	Nfam1<em1(IMPC)Ccpcz>/Nfam1<em1(IMPC)Ccpcz>	C57BL/6N-Nfam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731388	F	MP:0009709	hydrometra	Nfam1<em1(IMPC)Ccpcz>/Nfam1<em1(IMPC)Ccpcz>	C57BL/6N-Nfam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731388	F	MP:0001120	abnormal uterus morphology	Nfam1<em1(IMPC)Ccpcz>/Nfam1<em1(IMPC)Ccpcz>	C57BL/6N-Nfam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731388	F	MP:0000703	abnormal thymus morphology	Nfam1<em1(IMPC)Ccpcz>/Nfam1<em1(IMPC)Ccpcz>	C57BL/6N-Nfam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731389	M	MP:0000266	abnormal heart morphology	Niban1<em1(IMPC)Ccpcz>/Niban1<em1(IMPC)Ccpcz>	C57BL/6N-Niban1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731389	M	MP:0011496	abnormal head size	Niban1<em1(IMPC)Ccpcz>/Niban1<em1(IMPC)Ccpcz>	C57BL/6N-Niban1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731389	F	MP:0004906	enlarged uterus	Niban1<em1(IMPC)Ccpcz>/Niban1<em1(IMPC)Ccpcz>	C57BL/6N-Niban1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731389	F	MP:0001120	abnormal uterus morphology	Niban1<em1(IMPC)Ccpcz>/Niban1<em1(IMPC)Ccpcz>	C57BL/6N-Niban1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731389	M	MP:0000274	enlarged heart	Niban1<em1(IMPC)Ccpcz>/Niban1<em1(IMPC)Ccpcz>	C57BL/6N-Niban1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731389	F	MP:0002060	abnormal skin morphology	Niban1<em1(IMPC)Ccpcz>/Niban1<em1(IMPC)Ccpcz>	C57BL/6N-Niban1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731397	F	MP:0005562	decreased mean corpuscular hemoglobin	Pcdhb10<em1(IMPC)Tcp>/Pcdhb10<em1(IMPC)Tcp>	C57BL/6N-Pcdhb10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731397	F	MP:0002591	decreased mean corpuscular volume	Pcdhb10<em1(IMPC)Tcp>/Pcdhb10<em1(IMPC)Tcp>	C57BL/6N-Pcdhb10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731397	M	MP:0002092	abnormal eye morphology	Pcdhb10<em1(IMPC)Tcp>/Pcdhb10<em1(IMPC)Tcp>	C57BL/6N-Pcdhb10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731398	F	MP:0001399	hyperactivity	Pcgf3<em1(IMPC)Bay>/Pcgf3<+>	C57BL/6N-Pcgf3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731398	F	MP:0009142	decreased prepulse inhibition	Pcgf3<em1(IMPC)Bay>/Pcgf3<+>	C57BL/6N-Pcgf3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731399	F	MP:0001297	microphthalmia	Pcgf3<em1(IMPC)Bay>/Pcgf3<em1(IMPC)Bay>	C57BL/6N-Pcgf3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731400	F	MP:0001399	hyperactivity	Pdxp<em1(IMPC)J>/Pdxp<em1(IMPC)J>	C57BL/6NJ-Pdxp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731400	M	MP:0003960	increased lean body mass	Pdxp<em1(IMPC)J>/Pdxp<em1(IMPC)J>	C57BL/6NJ-Pdxp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731400	M	MP:0000218	increased leukocyte cell number	Pdxp<em1(IMPC)J>/Pdxp<em1(IMPC)J>	C57BL/6NJ-Pdxp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731400	F	MP:0010124	decreased bone mineral content	Pdxp<em1(IMPC)J>/Pdxp<em1(IMPC)J>	C57BL/6NJ-Pdxp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731400	F	MP:0003795	abnormal bone structure	Pdxp<em1(IMPC)J>/Pdxp<em1(IMPC)J>	C57BL/6NJ-Pdxp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731403	M	MP:0000157	abnormal sternum morphology	Phka1<em1(IMPC)Tcp>/Y	C57BL/6N-Phka1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731403	M	MP:0000692	small spleen	Phka1<em1(IMPC)Tcp>/Y	C57BL/6N-Phka1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731403	M	MP:0002060	abnormal skin morphology	Phka1<em1(IMPC)Tcp>/Y	C57BL/6N-Phka1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731404	M	MP:0005559	increased circulating glucose level	Pigz<em1(IMPC)J>/Pigz<em1(IMPC)J>	C57BL/6NJ-Pigz<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731404	M	MP:0010024	increased total body fat amount	Pigz<em1(IMPC)J>/Pigz<em1(IMPC)J>	C57BL/6NJ-Pigz<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731404	M	MP:0010124	decreased bone mineral content	Pigz<em1(IMPC)J>/Pigz<em1(IMPC)J>	C57BL/6NJ-Pigz<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731405	F	MP:0003795	abnormal bone structure	Pitpnm3<em1(IMPC)Bay>/Pitpnm3<em1(IMPC)Bay>	C57BL/6N-Pitpnm3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731406	F	MP:0009142	decreased prepulse inhibition	Pjvk<em1(IMPC)J>/Pjvk<em1(IMPC)J>	C57BL/6NJ-Pjvk<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731406	F	MP:0001399	hyperactivity	Pjvk<em1(IMPC)J>/Pjvk<em1(IMPC)J>	C57BL/6NJ-Pjvk<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731406	F	MP:0001410	head bobbing	Pjvk<em1(IMPC)J>/Pjvk<em1(IMPC)J>	C57BL/6NJ-Pjvk<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731410	M	MP:0000221	decreased leukocyte cell number	Pold4<em1(IMPC)J>/Pold4<em1(IMPC)J>	C57BL/6NJ-Pold4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731410	M	MP:0000195	decreased circulating calcium level	Pold4<em1(IMPC)J>/Pold4<em1(IMPC)J>	C57BL/6NJ-Pold4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731411	M	MP:0001284	absent vibrissae	Polr2l<em1(IMPC)J>/Polr2l<+>	C57BL/6NJ-Polr2l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731411	F	MP:0001399	hyperactivity	Polr2l<em1(IMPC)J>/Polr2l<+>	C57BL/6NJ-Polr2l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731412	F	MP:0001697	abnormal embryo size	Polr3gl<em1(IMPC)Bay>/Polr3gl<em1(IMPC)Bay>	C57BL/6N-Polr3gl<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731413	M	MP:0001552	increased circulating triglyceride level	Pon3<tm1b(KOMP)Wtsi>/Pon3<tm1b(KOMP)Wtsi>	C57BL/6N-Pon3<tm1b(KOMP)Wtsi>/Kmpc	N	MGI:5576271
MGI:6731414	F	MP:0011110	preweaning lethality, incomplete penetrance	Prdm15<tm1b(EUCOMM)Wtsi>/Prdm15<tm1b(EUCOMM)Wtsi>	C57BL/6N-Prdm15<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6731416	M	MP:0000689	abnormal spleen morphology	Prss21<em1(IMPC)Ccpcz>/Prss21<+>	C57BL/6N-Prss21<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731416	F	MP:0009709	hydrometra	Prss21<em1(IMPC)Ccpcz>/Prss21<+>	C57BL/6N-Prss21<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731416	F	MP:0000709	enlarged thymus	Prss21<em1(IMPC)Ccpcz>/Prss21<+>	C57BL/6N-Prss21<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731416	M	MP:0000274	enlarged heart	Prss21<em1(IMPC)Ccpcz>/Prss21<+>	C57BL/6N-Prss21<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731416	M	MP:0000266	abnormal heart morphology	Prss21<em1(IMPC)Ccpcz>/Prss21<+>	C57BL/6N-Prss21<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731416	F	MP:0001120	abnormal uterus morphology	Prss21<em1(IMPC)Ccpcz>/Prss21<+>	C57BL/6N-Prss21<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731416	F	MP:0000703	abnormal thymus morphology	Prss21<em1(IMPC)Ccpcz>/Prss21<+>	C57BL/6N-Prss21<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731418	F	MP:0002060	abnormal skin morphology	Prss33<em1(IMPC)Ccpcz>/Prss33<em1(IMPC)Ccpcz>	C57BL/6N-Prss33<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731418	F	MP:0001120	abnormal uterus morphology	Prss33<em1(IMPC)Ccpcz>/Prss33<em1(IMPC)Ccpcz>	C57BL/6N-Prss33<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731418	M	MP:0001262	decreased body weight	Prss33<em1(IMPC)Ccpcz>/Prss33<em1(IMPC)Ccpcz>	C57BL/6N-Prss33<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731418	F	MP:0004906	enlarged uterus	Prss33<em1(IMPC)Ccpcz>/Prss33<em1(IMPC)Ccpcz>	C57BL/6N-Prss33<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731418	M	MP:0001147	small testis	Prss33<em1(IMPC)Ccpcz>/Prss33<em1(IMPC)Ccpcz>	C57BL/6N-Prss33<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731418	F	MP:0000691	enlarged spleen	Prss33<em1(IMPC)Ccpcz>/Prss33<em1(IMPC)Ccpcz>	C57BL/6N-Prss33<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731418	M	MP:0001146	abnormal testis morphology	Prss33<em1(IMPC)Ccpcz>/Prss33<em1(IMPC)Ccpcz>	C57BL/6N-Prss33<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731418	M	MP:0000692	small spleen	Prss33<em1(IMPC)Ccpcz>/Prss33<em1(IMPC)Ccpcz>	C57BL/6N-Prss33<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731419	F	MP:0001120	abnormal uterus morphology	Prss35<em1(IMPC)Ccpcz>/Prss35<em1(IMPC)Ccpcz>	C57BL/6N-Prss35<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731419	M	MP:0001147	small testis	Prss35<em1(IMPC)Ccpcz>/Prss35<em1(IMPC)Ccpcz>	C57BL/6N-Prss35<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731419	M	MP:0000162	lordosis	Prss35<em1(IMPC)Ccpcz>/Prss35<em1(IMPC)Ccpcz>	C57BL/6N-Prss35<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731419	F	MP:0001402	decreased locomotor activity	Prss35<em1(IMPC)Ccpcz>/Prss35<em1(IMPC)Ccpcz>	C57BL/6N-Prss35<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731419	F	MP:0002060	abnormal skin morphology	Prss35<em1(IMPC)Ccpcz>/Prss35<em1(IMPC)Ccpcz>	C57BL/6N-Prss35<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731419	F	MP:0009709	hydrometra	Prss35<em1(IMPC)Ccpcz>/Prss35<em1(IMPC)Ccpcz>	C57BL/6N-Prss35<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731419	M	MP:0000703	abnormal thymus morphology	Prss35<em1(IMPC)Ccpcz>/Prss35<em1(IMPC)Ccpcz>	C57BL/6N-Prss35<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731419	M	MP:0005293	impaired glucose tolerance	Prss35<em1(IMPC)Ccpcz>/Prss35<em1(IMPC)Ccpcz>	C57BL/6N-Prss35<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731419	M	MP:0000691	enlarged spleen	Prss35<em1(IMPC)Ccpcz>/Prss35<em1(IMPC)Ccpcz>	C57BL/6N-Prss35<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731419	M	MP:0000274	enlarged heart	Prss35<em1(IMPC)Ccpcz>/Prss35<em1(IMPC)Ccpcz>	C57BL/6N-Prss35<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731419	M	MP:0000160	kyphosis	Prss35<em1(IMPC)Ccpcz>/Prss35<em1(IMPC)Ccpcz>	C57BL/6N-Prss35<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731419	M	MP:0000266	abnormal heart morphology	Prss35<em1(IMPC)Ccpcz>/Prss35<em1(IMPC)Ccpcz>	C57BL/6N-Prss35<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731419	M	MP:0000709	enlarged thymus	Prss35<em1(IMPC)Ccpcz>/Prss35<em1(IMPC)Ccpcz>	C57BL/6N-Prss35<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731420	F	MP:0000703	abnormal thymus morphology	Prss57<em1(IMPC)Ccpcz>/Prss57<em1(IMPC)Ccpcz>	C57BL/6N-Prss57<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731420	M	MP:0011047	increased lung tissue damping	Prss57<em1(IMPC)Ccpcz>/Prss57<em1(IMPC)Ccpcz>	C57BL/6N-Prss57<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731420	F	MP:0009709	hydrometra	Prss57<em1(IMPC)Ccpcz>/Prss57<em1(IMPC)Ccpcz>	C57BL/6N-Prss57<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731420	F	MP:0000709	enlarged thymus	Prss57<em1(IMPC)Ccpcz>/Prss57<em1(IMPC)Ccpcz>	C57BL/6N-Prss57<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731420	F	MP:0001120	abnormal uterus morphology	Prss57<em1(IMPC)Ccpcz>/Prss57<em1(IMPC)Ccpcz>	C57BL/6N-Prss57<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731422	M	MP:0005293	impaired glucose tolerance	Pwwp2b<em1(IMPC)J>/Pwwp2b<em1(IMPC)J>	C57BL/6NJ-Pwwp2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731424	F	MP:0011110	preweaning lethality, incomplete penetrance	Rbm34<tm1b(EUCOMM)Hmgu>/Rbm34<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rbm34<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6731425	F	MP:0003743	abnormal facial morphology	Rbm45<em1(IMPC)J>/Rbm45<em1(IMPC)J>	C57BL/6NJ-Rbm45<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731426	F	MP:0005011	increased eosinophil cell number	Rgs4<em1(IMPC)H>/Rgs4<em1(IMPC)H>	C57BL/6N-Rgs4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731426	F	MP:0005016	decreased lymphocyte cell number	Rgs4<em1(IMPC)H>/Rgs4<em1(IMPC)H>	C57BL/6N-Rgs4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731426	F	MP:0004952	increased spleen weight	Rgs4<em1(IMPC)H>/Rgs4<em1(IMPC)H>	C57BL/6N-Rgs4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731426	F	MP:0002590	increased mean corpuscular volume	Rgs4<em1(IMPC)H>/Rgs4<em1(IMPC)H>	C57BL/6N-Rgs4<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731427	M	MP:0001399	hyperactivity	Rgs8<em1(IMPC)H>/Rgs8<em1(IMPC)H>	C57BL/6NTac-Rgs8<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731429	M	MP:0010052	increased grip strength	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	M	MP:0005343	increased circulating aspartate transaminase level	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	F	MP:0005084	abnormal gallbladder morphology	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	F	MP:0000703	abnormal thymus morphology	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	F	MP:0010090	increased circulating creatine kinase level	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	F	MP:0005011	increased eosinophil cell number	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	F	MP:0000266	abnormal heart morphology	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	M	MP:0001262	decreased body weight	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	M	MP:0000702	enlarged lymph nodes	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	M	MP:0011047	increased lung tissue damping	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	M	MP:0002339	abnormal lymph node morphology	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	F	MP:0000709	enlarged thymus	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	M	MP:0002941	increased circulating alanine transaminase level	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	F	MP:0000274	enlarged heart	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731429	F	MP:0009342	enlarged gallbladder	Rnf208<em1(IMPC)Ccpcz>/Rnf208<em1(IMPC)Ccpcz>	C57BL/6N-Rnf208<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731430	M	MP:0011110	preweaning lethality, incomplete penetrance	Rpusd3<em1(IMPC)Bay>/Rpusd3<em1(IMPC)Bay>	C57BL/6N-Rpusd3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731430	M	MP:0010123	increased bone mineral content	Rpusd3<em1(IMPC)Bay>/Rpusd3<em1(IMPC)Bay>	C57BL/6N-Rpusd3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731432	M	MP:0005565	increased blood urea nitrogen level	Samd3<em1(IMPC)H>/Samd3<em1(IMPC)H>	C57BL/6N-Samd3<em1(IMPC)H>/H	N	MGI:5576271
MGI:6731433	F	MP:0010123	increased bone mineral content	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	F	MP:0010052	increased grip strength	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0001364	decreased anxiety-related response	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0004924	abnormal behavior	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0001925	male infertility	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0002966	decreased circulating alkaline phosphatase level	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0001146	abnormal testis morphology	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0003068	enlarged kidney	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	F	MP:0013278	decreased fasting circulating glucose level	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0000274	enlarged heart	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0000266	abnormal heart morphology	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0020870	decreased thigmotaxis	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0010067	increased red blood cell distribution width	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0005016	decreased lymphocyte cell number	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0001147	small testis	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0001399	hyperactivity	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	F	MP:0000601	small liver	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0009552	urinary bladder obstruction	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0000219	increased neutrophil cell number	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	M	MP:0002135	abnormal kidney morphology	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731433	F	MP:0000598	abnormal liver morphology	Sbf1<em1(IMPC)Mbp>/Sbf1<em1(IMPC)Mbp>	C57BL/6N-Sbf1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731434	M	MP:0004952	increased spleen weight	Scn8a<em1(IMPC)Bay>/Scn8a<+>	C57BL/6N-Scn8a<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731436	M	MP:0002965	increased circulating serum albumin level	Sh3rf3<em1(IMPC)J>/Sh3rf3<em1(IMPC)J>	C57BL/6NJ-Sh3rf3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731438	M	MP:0005293	impaired glucose tolerance	Slc26a2<em1(IMPC)Bay>/Slc26a2<+>	C57BL/6N-Slc26a2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731439	M	MP:0000063	decreased bone mineral density	Slc30a7<em1(IMPC)Bay>/Slc30a7<em1(IMPC)Bay>	C57BL/6N-Slc30a7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731439	M	MP:0005293	impaired glucose tolerance	Slc30a7<em1(IMPC)Bay>/Slc30a7<em1(IMPC)Bay>	C57BL/6N-Slc30a7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731439	M	MP:0000280	thin ventricular wall	Slc30a7<em1(IMPC)Bay>/Slc30a7<em1(IMPC)Bay>	C57BL/6N-Slc30a7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731439	M	MP:0003961	decreased lean body mass	Slc30a7<em1(IMPC)Bay>/Slc30a7<em1(IMPC)Bay>	C57BL/6N-Slc30a7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731439	M	MP:0011962	increased cornea thickness	Slc30a7<em1(IMPC)Bay>/Slc30a7<em1(IMPC)Bay>	C57BL/6N-Slc30a7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731439	M	MP:0010024	increased total body fat amount	Slc30a7<em1(IMPC)Bay>/Slc30a7<em1(IMPC)Bay>	C57BL/6N-Slc30a7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731440	F	MP:0011100	preweaning lethality, complete penetrance	Slc38a3<em1(IMPC)Bay>/Slc38a3<em1(IMPC)Bay>	C57BL/6N-Slc38a3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731443	M	MP:0000274	enlarged heart	Sox14<em1(IMPC)Ccpcz>/Sox14<+>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731443	M	MP:0002092	abnormal eye morphology	Sox14<em1(IMPC)Ccpcz>/Sox14<+>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731443	F	MP:0000703	abnormal thymus morphology	Sox14<em1(IMPC)Ccpcz>/Sox14<+>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731443	M	MP:0001297	microphthalmia	Sox14<em1(IMPC)Ccpcz>/Sox14<+>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731443	F	MP:0002188	small heart	Sox14<em1(IMPC)Ccpcz>/Sox14<+>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731443	F	MP:0000709	enlarged thymus	Sox14<em1(IMPC)Ccpcz>/Sox14<+>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731443	F	MP:0011047	increased lung tissue damping	Sox14<em1(IMPC)Ccpcz>/Sox14<+>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731443	F	MP:0002989	small kidney	Sox14<em1(IMPC)Ccpcz>/Sox14<+>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	M	MP:0010935	increased airway resistance	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	F	MP:0000703	abnormal thymus morphology	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	F	MP:0000443	abnormal snout morphology	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	M	MP:0010379	decreased respiratory quotient	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	F	MP:0000709	enlarged thymus	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	M	MP:0002059	abnormal seminal vesicle morphology	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	F	MP:0002339	abnormal lymph node morphology	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	M	MP:0001262	decreased body weight	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	M	MP:0001529	abnormal vocalization	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	F	MP:0002989	small kidney	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	F	MP:0002092	abnormal eye morphology	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	F	MP:0000689	abnormal spleen morphology	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	F	MP:0001402	decreased locomotor activity	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	M	MP:0001157	small seminal vesicle	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	M	MP:0001406	abnormal gait	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	M	MP:0001925	male infertility	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	F	MP:0020421	increased freezing behavior	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	M	MP:0001513	limb grasping	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	M	MP:0001512	trunk curl	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	F	MP:0002060	abnormal skin morphology	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	M	MP:0005655	increased aggression	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	F	MP:0001297	microphthalmia	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731444	F	MP:0000702	enlarged lymph nodes	Sox14<em1(IMPC)Ccpcz>/Sox14<em1(IMPC)Ccpcz>	C57BL/6N-Sox14<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0001293	anophthalmia	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0001402	decreased locomotor activity	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0013520	increased CD4-positive NK T cell number	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	M	MP:0000438	abnormal cranium morphology	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0013523	increased memory-marker CD4-positive NK T cell number	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0013772	increased effector memory T-helper cell number	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0000702	enlarged lymph nodes	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0002092	abnormal eye morphology	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0008039	increased NK T cell number	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0004613	fusion of vertebral arches	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0000137	abnormal vertebrae morphology	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	M	MP:0001486	abnormal startle reflex	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	M	MP:0004599	abnormal vertebral arch morphology	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	M	MP:0005627	increased circulating potassium level	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0010090	increased circulating creatine kinase level	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	M	MP:0001157	small seminal vesicle	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	M	MP:0002059	abnormal seminal vesicle morphology	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0005343	increased circulating aspartate transaminase level	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	M	MP:0000274	enlarged heart	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	M	MP:0003795	abnormal bone structure	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0002966	decreased circulating alkaline phosphatase level	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0002941	increased circulating alanine transaminase level	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	M	MP:0000266	abnormal heart morphology	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0002339	abnormal lymph node morphology	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	M	MP:0000458	abnormal mandible morphology	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	M	MP:0002060	abnormal skin morphology	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0001126	abnormal ovary morphology	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731445	F	MP:0011239	abnormal skin coloration	Spred1<em1(IMPC)Ccpcz>/Spred1<em1(IMPC)Ccpcz>	C57BL/6N-Spred1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731448	M	MP:0005292	improved glucose tolerance	Sytl4<em1(IMPC)Hmgu>/Y	C57BL/6N-Sytl4<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6731450	F	MP:0001293	anophthalmia	Taar8c<em1(IMPC)Mbp>/Taar8c<em1(IMPC)Mbp>	C57BL/6N-Taar8c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731450	M	MP:0001200	thick skin	Taar8c<em1(IMPC)Mbp>/Taar8c<em1(IMPC)Mbp>	C57BL/6N-Taar8c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731450	F	MP:0002092	abnormal eye morphology	Taar8c<em1(IMPC)Mbp>/Taar8c<em1(IMPC)Mbp>	C57BL/6N-Taar8c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731450	M	MP:0002060	abnormal skin morphology	Taar8c<em1(IMPC)Mbp>/Taar8c<em1(IMPC)Mbp>	C57BL/6N-Taar8c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731450	F	MP:0000598	abnormal liver morphology	Taar8c<em1(IMPC)Mbp>/Taar8c<em1(IMPC)Mbp>	C57BL/6N-Taar8c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731450	F	MP:0000601	small liver	Taar8c<em1(IMPC)Mbp>/Taar8c<em1(IMPC)Mbp>	C57BL/6N-Taar8c<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6731451	F	MP:0010052	increased grip strength	Taf5<em1(IMPC)J>/Taf5<+>	C57BL/6NJ-Taf5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731451	M	MP:0010024	increased total body fat amount	Taf5<em1(IMPC)J>/Taf5<+>	C57BL/6NJ-Taf5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731452	M	MP:0001297	microphthalmia	Tagap1<em1(IMPC)Tcp>/Tagap1<+>	C57BL/6N-Tagap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731452	M	MP:0002060	abnormal skin morphology	Tagap1<em1(IMPC)Tcp>/Tagap1<+>	C57BL/6N-Tagap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731452	M	MP:0000691	enlarged spleen	Tagap1<em1(IMPC)Tcp>/Tagap1<+>	C57BL/6N-Tagap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731452	M	MP:0000702	enlarged lymph nodes	Tagap1<em1(IMPC)Tcp>/Tagap1<+>	C57BL/6N-Tagap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731452	M	MP:0003068	enlarged kidney	Tagap1<em1(IMPC)Tcp>/Tagap1<+>	C57BL/6N-Tagap1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731455	M	MP:0000221	decreased leukocyte cell number	Tcea2<em1(IMPC)J>/Tcea2<em1(IMPC)J>	C57BL/6NJ-Tcea2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731455	M	MP:0000195	decreased circulating calcium level	Tcea2<em1(IMPC)J>/Tcea2<em1(IMPC)J>	C57BL/6NJ-Tcea2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731455	F	MP:0001399	hyperactivity	Tcea2<em1(IMPC)J>/Tcea2<em1(IMPC)J>	C57BL/6NJ-Tcea2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731455	F	MP:0002075	abnormal coat/hair pigmentation	Tcea2<em1(IMPC)J>/Tcea2<em1(IMPC)J>	C57BL/6NJ-Tcea2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731456	M	MP:0001399	hyperactivity	Tchh<em1(IMPC)J>/Tchh<em1(IMPC)J>	C57BL/6NJ-Tchh<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731457	M	MP:0001399	hyperactivity	Tdrd3<em1(IMPC)J>/Tdrd3<em1(IMPC)J>	C57BL/6NJ-Tdrd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731458	M	MP:0005333	decreased heart rate	Tex21<em1(IMPC)J>/Tex21<em1(IMPC)J>	C57BL/6NJ-Tex21<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731461	M	MP:0000579	abnormal nail morphology	Tmem147<em1(IMPC)J>/Tmem147<+>	C57BL/6NJ-Tmem147<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731463	M	MP:0000367	abnormal coat/ hair morphology	Tmem33<em1(IMPC)J>/Tmem33<em1(IMPC)J>	C57BL/6NJ-Tmem33<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731463	F	MP:0002574	increased vertical activity	Tmem33<em1(IMPC)J>/Tmem33<em1(IMPC)J>	C57BL/6NJ-Tmem33<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731466	F	MP:0002968	increased circulating alkaline phosphatase level	Tpd52l1<em1(IMPC)J>/Tpd52l1<em1(IMPC)J>	C57BL/6NJ-Tpd52l1<em1(IMPC)J>/J	N	MGI:5576271
MGI:6731469	M	MP:0000288	abnormal pericardium morphology	Traf3ip1<em1(IMPC)Bay>/Traf3ip1<em1(IMPC)Bay>	C57BL/6N-Traf3ip1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731469	M	MP:0000266	abnormal heart morphology	Traf3ip1<em1(IMPC)Bay>/Traf3ip1<em1(IMPC)Bay>	C57BL/6N-Traf3ip1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731469	M	MP:0001691	abnormal somite shape	Traf3ip1<em1(IMPC)Bay>/Traf3ip1<em1(IMPC)Bay>	C57BL/6N-Traf3ip1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731469	M	MP:0001700	abnormal embryo turning	Traf3ip1<em1(IMPC)Bay>/Traf3ip1<em1(IMPC)Bay>	C57BL/6N-Traf3ip1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731469	M	MP:0001697	abnormal embryo size	Traf3ip1<em1(IMPC)Bay>/Traf3ip1<em1(IMPC)Bay>	C57BL/6N-Traf3ip1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731469	M	MP:0001785	edema	Traf3ip1<em1(IMPC)Bay>/Traf3ip1<em1(IMPC)Bay>	C57BL/6N-Traf3ip1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731469	M	MP:0003984	embryonic growth retardation	Traf3ip1<em1(IMPC)Bay>/Traf3ip1<em1(IMPC)Bay>	C57BL/6N-Traf3ip1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731470	F	MP:0001314	cornea opacity	Trim33<em1(IMPC)Tcp>/Trim33<+>	C57BL/6N-Trim33<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731470	M	MP:0000702	enlarged lymph nodes	Trim33<em1(IMPC)Tcp>/Trim33<+>	C57BL/6N-Trim33<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6731471	F	MP:0010097	abnormal retina blood vessel morphology	Trim68<em1(IMPC)J>/Trim68<em1(IMPC)J>	C57BL/6NJ-Trim68<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731474	F	MP:0000691	enlarged spleen	Trip6<tm1b(EUCOMM)Hmgu>/Trip6<+>	C57BL/6N-Trip6<tm1b(EUCOMM)Hmgu>/Bay	N	MGI:5576271
MGI:6731476	F	MP:0002968	increased circulating alkaline phosphatase level	Tuba1c<em1(IMPC)J>/Tuba1c<em1(IMPC)J>	C57BL/6NJ-Tuba1c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731479	F	MP:0005278	abnormal cholesterol homeostasis	U2af2<em1(IMPC)J>/U2af2<+>	C57BL/6NJ-U2af2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731481	M	MP:0001322	abnormal iris morphology	Ube3b<em1(IMPC)Bay>/Ube3b<+>	C57BL/6N-Ube3b<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6731481	M	MP:0011962	increased cornea thickness	Ube3b<em1(IMPC)Bay>/Ube3b<+>	C57BL/6N-Ube3b<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6731481	M	MP:0001312	abnormal cornea morphology	Ube3b<em1(IMPC)Bay>/Ube3b<+>	C57BL/6N-Ube3b<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6731481	M	MP:0001307	fused cornea and lens	Ube3b<em1(IMPC)Bay>/Ube3b<+>	C57BL/6N-Ube3b<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6731481	M	MP:0004222	iris synechia	Ube3b<em1(IMPC)Bay>/Ube3b<+>	C57BL/6N-Ube3b<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6731481	F	MP:0003733	abnormal retina inner nuclear layer morphology	Ube3b<em1(IMPC)Bay>/Ube3b<+>	C57BL/6N-Ube3b<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6731481	F	MP:0011960	abnormal eye anterior chamber depth	Ube3b<em1(IMPC)Bay>/Ube3b<+>	C57BL/6N-Ube3b<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6731481	M	MP:0001303	abnormal lens morphology	Ube3b<em1(IMPC)Bay>/Ube3b<+>	C57BL/6N-Ube3b<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6731481	M	MP:0006203	eye hemorrhage	Ube3b<em1(IMPC)Bay>/Ube3b<+>	C57BL/6N-Ube3b<em1(IMPC)Bay>/Bay	N	MGI:5576271
MGI:6731492	F	MP:0000709	enlarged thymus	Zc2hc1c<em1(IMPC)Ccpcz>/Zc2hc1c<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731492	M	MP:0000266	abnormal heart morphology	Zc2hc1c<em1(IMPC)Ccpcz>/Zc2hc1c<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731492	M	MP:0001148	enlarged testis	Zc2hc1c<em1(IMPC)Ccpcz>/Zc2hc1c<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731492	F	MP:0001120	abnormal uterus morphology	Zc2hc1c<em1(IMPC)Ccpcz>/Zc2hc1c<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731492	F	MP:0009709	hydrometra	Zc2hc1c<em1(IMPC)Ccpcz>/Zc2hc1c<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731492	M	MP:0001146	abnormal testis morphology	Zc2hc1c<em1(IMPC)Ccpcz>/Zc2hc1c<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731492	M	MP:0000274	enlarged heart	Zc2hc1c<em1(IMPC)Ccpcz>/Zc2hc1c<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731492	F	MP:0000160	kyphosis	Zc2hc1c<em1(IMPC)Ccpcz>/Zc2hc1c<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731492	M	MP:0002092	abnormal eye morphology	Zc2hc1c<em1(IMPC)Ccpcz>/Zc2hc1c<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731492	F	MP:0004174	abnormal spine curvature	Zc2hc1c<em1(IMPC)Ccpcz>/Zc2hc1c<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731492	F	MP:0000703	abnormal thymus morphology	Zc2hc1c<em1(IMPC)Ccpcz>/Zc2hc1c<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731492	M	MP:0001147	small testis	Zc2hc1c<em1(IMPC)Ccpcz>/Zc2hc1c<em1(IMPC)Ccpcz>	C57BL/6N-Zc2hc1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:6731493	M	MP:0001925	male infertility	Zdhhc19<em1(IMPC)J>/Zdhhc19<em1(IMPC)J>	C57BL/6NJ-Zdhhc19<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731499	M	MP:0010123	increased bone mineral content	Zfp654<em1(IMPC)Bay>/Zfp654<+>	C57BL/6N-Zfp654<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6731501	M	MP:0001325	abnormal retina morphology	Zfp729b<em1(IMPC)J>/Zfp729b<em1(IMPC)J>	C57BL/6NJ-Zfp729b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6731501	F	MP:0005562	decreased mean corpuscular hemoglobin	Zfp729b<em1(IMPC)J>/Zfp729b<em1(IMPC)J>	C57BL/6NJ-Zfp729b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6740229	M	MP:0005389	reproductive system phenotype	4930524B15Rik<em1Qsh>/4930524B15Rik<em1Qsh>	Not Specified	Y	32592116
MGI:6741540	M	MP:0008545	absent sperm flagellum	Bbs5<tm1a(EUCOMM)Wtsi>/Bbs5<tm1a(EUCOMM)Wtsi>	C57BL/6-Bbs5<tm1a(EUCOMM)Wtsi>	N	33560420
MGI:6742268	M	MP:0004357	long tibia	St6gal2<em1(IMPC)H>/St6gal2<em1(IMPC)H>	C57BL/6N-St6gal2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6742268	F	MP:0009455	enhanced cued conditioning behavior	St6gal2<em1(IMPC)H>/St6gal2<em1(IMPC)H>	C57BL/6N-St6gal2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6753229	F	MP:0001392	abnormal locomotor behavior	Mb<em1Shad>/Mb<em1Shad>	B6N-Mb<em1Shad>	N	33969704
MGI:6753229	F	MP:0020330	increased capillary density	Mb<em1Shad>/Mb<em1Shad>	B6N-Mb<em1Shad>	N	33969704
MGI:6753229	M	MP:0020330	increased capillary density	Mb<em1Shad>/Mb<em1Shad>	B6N-Mb<em1Shad>	N	33969704
MGI:6753229	M	MP:0001392	abnormal locomotor behavior	Mb<em1Shad>/Mb<em1Shad>	B6N-Mb<em1Shad>	N	33969704
MGI:6753390	M	MP:0005389	reproductive system phenotype	4930579G24Rik<em1Qsh>/4930579G24Rik<em1Qsh>	C57BL/6-4930579G24Rik<em1Qsh>	Y	34076717
MGI:6755500	M	MP:0006380	abnormal spermatid morphology	Fis1<tm1Dcc>/Fis1<tm1.1Dcc>,Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Tg(Stra8-icre)1Reb/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ	N	34355730
MGI:6755500	M	MP:0004852	decreased testis weight	Fis1<tm1Dcc>/Fis1<tm1.1Dcc>,Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Tg(Stra8-icre)1Reb/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ	N	34355730
MGI:6755500	M	MP:0005159	azoospermia	Fis1<tm1Dcc>/Fis1<tm1.1Dcc>,Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Tg(Stra8-icre)1Reb/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ	N	34355730
MGI:6755500	M	MP:0020550	multinucleated giant male germ cells	Fis1<tm1Dcc>/Fis1<tm1.1Dcc>,Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Tg(Stra8-icre)1Reb/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ	N	34355730
MGI:6755500	M	MP:0001147	small testis	Fis1<tm1Dcc>/Fis1<tm1.1Dcc>,Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Tg(Stra8-icre)1Reb/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ	N	34355730
MGI:6755500	M	MP:0011628	increased mitochondrial number	Fis1<tm1Dcc>/Fis1<tm1.1Dcc>,Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Tg(Stra8-icre)1Reb/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ	N	34355730
MGI:6755500	M	MP:0030940	impaired autophagy	Fis1<tm1Dcc>/Fis1<tm1.1Dcc>,Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Tg(Stra8-icre)1Reb/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ	N	34355730
MGI:6755500	M	MP:0014052	increased male germ cell apoptosis	Fis1<tm1Dcc>/Fis1<tm1.1Dcc>,Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Tg(Stra8-icre)1Reb/0	involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ	N	34355730
MGI:6756378	F	MP:0003900	shortened QT interval	Strip2<tm1.2Tac>/Strip2<tm1.2Tac>	Not Specified	N	27122098
MGI:6757251	F	MP:0008950	ventricular tachycardia	Obscn<tm1.1Geno>/Obscn<tm1.1Geno>	B6.129-Obscn<tm1.1Geno>	N	28630914
MGI:6757251	F	MP:0002626	increased heart rate	Obscn<tm1.1Geno>/Obscn<tm1.1Geno>	B6.129-Obscn<tm1.1Geno>	N	28630914
MGI:6757251	F	MP:0004485	increased response of heart to induced stress	Obscn<tm1.1Geno>/Obscn<tm1.1Geno>	B6.129-Obscn<tm1.1Geno>	N	28630914
MGI:6757251	F	MP:0004215	abnormal myocardial fiber physiology	Obscn<tm1.1Geno>/Obscn<tm1.1Geno>	B6.129-Obscn<tm1.1Geno>	N	28630914
MGI:6757251	F	MP:0009732	ventricular premature beat	Obscn<tm1.1Geno>/Obscn<tm1.1Geno>	B6.129-Obscn<tm1.1Geno>	N	28630914
MGI:6757251	F	MP:0031635	increased heart left ventricle muscle contractility	Obscn<tm1.1Geno>/Obscn<tm1.1Geno>	B6.129-Obscn<tm1.1Geno>	N	28630914
MGI:6758251	M	MP:0002687	oligozoospermia	Usp26<tm1Smoc>/Y	B6.129S6-Usp26<tm1Smoc>	N	30561524
MGI:6758251	M	MP:0001156	abnormal spermatogenesis	Usp26<tm1Smoc>/Y	B6.129S6-Usp26<tm1Smoc>	N	30561524
MGI:6758251	M	MP:0001146	abnormal testis morphology	Usp26<tm1Smoc>/Y	B6.129S6-Usp26<tm1Smoc>	N	30561524
MGI:6758251	M	MP:0001922	reduced male fertility	Usp26<tm1Smoc>/Y	B6.129S6-Usp26<tm1Smoc>	N	30561524
MGI:6758251	M	MP:0002780	decreased circulating testosterone level	Usp26<tm1Smoc>/Y	B6.129S6-Usp26<tm1Smoc>	N	30561524
MGI:6758251	M	MP:0001751	increased circulating luteinizing hormone level	Usp26<tm1Smoc>/Y	B6.129S6-Usp26<tm1Smoc>	N	30561524
MGI:6758251	M	MP:0002790	decreased circulating follicle stimulating hormone level	Usp26<tm1Smoc>/Y	B6.129S6-Usp26<tm1Smoc>	N	30561524
MGI:6758251	M	MP:0002216	abnormal seminiferous tubule morphology	Usp26<tm1Smoc>/Y	B6.129S6-Usp26<tm1Smoc>	N	30561524
MGI:6758251	M	MP:0004901	decreased male germ cell number	Usp26<tm1Smoc>/Y	B6.129S6-Usp26<tm1Smoc>	N	30561524
MGI:6758257	M	MP:0001147	small testis	Brd7<tm1.2Ligy>/Brd7<tm1.2Ligy>	involves: 129S4/SvJaeSor * C57BL/6J * FVB/N	N	26878912
MGI:6758257	M	MP:0005376	homeostasis/metabolism phenotype	Brd7<tm1.2Ligy>/Brd7<tm1.2Ligy>	involves: 129S4/SvJaeSor * C57BL/6J * FVB/N	Y	26878912
MGI:6758257	M	MP:0004852	decreased testis weight	Brd7<tm1.2Ligy>/Brd7<tm1.2Ligy>	involves: 129S4/SvJaeSor * C57BL/6J * FVB/N	N	26878912
MGI:6758257	M	MP:0008839	absent acrosome	Brd7<tm1.2Ligy>/Brd7<tm1.2Ligy>	involves: 129S4/SvJaeSor * C57BL/6J * FVB/N	N	26878912
MGI:6758257	M	MP:0001153	small seminiferous tubules	Brd7<tm1.2Ligy>/Brd7<tm1.2Ligy>	involves: 129S4/SvJaeSor * C57BL/6J * FVB/N	N	26878912
MGI:6758257	M	MP:0001925	male infertility	Brd7<tm1.2Ligy>/Brd7<tm1.2Ligy>	involves: 129S4/SvJaeSor * C57BL/6J * FVB/N	N	26878912
MGI:6758257	M	MP:0005159	azoospermia	Brd7<tm1.2Ligy>/Brd7<tm1.2Ligy>	involves: 129S4/SvJaeSor * C57BL/6J * FVB/N	N	26878912
MGI:6758257	M	MP:0014052	increased male germ cell apoptosis	Brd7<tm1.2Ligy>/Brd7<tm1.2Ligy>	involves: 129S4/SvJaeSor * C57BL/6J * FVB/N	N	26878912
MGI:6758257	M	MP:0006380	abnormal spermatid morphology	Brd7<tm1.2Ligy>/Brd7<tm1.2Ligy>	involves: 129S4/SvJaeSor * C57BL/6J * FVB/N	N	26878912
MGI:6758257	M	MP:0008898	abnormal acrosome morphology	Brd7<tm1.2Ligy>/Brd7<tm1.2Ligy>	involves: 129S4/SvJaeSor * C57BL/6J * FVB/N	N	26878912
MGI:6758257	M	MP:0001155	arrest of spermatogenesis	Brd7<tm1.2Ligy>/Brd7<tm1.2Ligy>	involves: 129S4/SvJaeSor * C57BL/6J * FVB/N	N	26878912
MGI:6758257	M	MP:0009230	abnormal sperm head morphology	Brd7<tm1.2Ligy>/Brd7<tm1.2Ligy>	involves: 129S4/SvJaeSor * C57BL/6J * FVB/N	N	26878912
MGI:6758257	M	MP:0002686	globozoospermia	Brd7<tm1.2Ligy>/Brd7<tm1.2Ligy>	involves: 129S4/SvJaeSor * C57BL/6J * FVB/N	N	26878912
MGI:6758504	F	MP:0001923	reduced female fertility	Strada<em1Pbcr>/Strada<+>	C57BL/6N-Strada<em1Pbcr>	N	32457579
MGI:6758665	M	MP:0002675	asthenozoospermia	Wdr62<tm3a(EUCOMM)Hmgu>/Wdr62<tm3a(EUCOMM)Hmgu>	C57BL/6-Wdr62<tm3a(EUCOMM)Hmgu>	N	34059773
MGI:6758665	M	MP:0005169	abnormal male meiosis	Wdr62<tm3a(EUCOMM)Hmgu>/Wdr62<tm3a(EUCOMM)Hmgu>	C57BL/6-Wdr62<tm3a(EUCOMM)Hmgu>	N	34059773
MGI:6758665	F	MP:0004805	absent oocytes	Wdr62<tm3a(EUCOMM)Hmgu>/Wdr62<tm3a(EUCOMM)Hmgu>	C57BL/6-Wdr62<tm3a(EUCOMM)Hmgu>	N	34059773
MGI:6758665	M	MP:0005578	teratozoospermia	Wdr62<tm3a(EUCOMM)Hmgu>/Wdr62<tm3a(EUCOMM)Hmgu>	C57BL/6-Wdr62<tm3a(EUCOMM)Hmgu>	N	34059773
MGI:6758665	M	MP:0002216	abnormal seminiferous tubule morphology	Wdr62<tm3a(EUCOMM)Hmgu>/Wdr62<tm3a(EUCOMM)Hmgu>	C57BL/6-Wdr62<tm3a(EUCOMM)Hmgu>	N	34059773
MGI:6758665	M	MP:0004852	decreased testis weight	Wdr62<tm3a(EUCOMM)Hmgu>/Wdr62<tm3a(EUCOMM)Hmgu>	C57BL/6-Wdr62<tm3a(EUCOMM)Hmgu>	N	34059773
MGI:6758665	M	MP:0020451	decreased sperm progressive motility	Wdr62<tm3a(EUCOMM)Hmgu>/Wdr62<tm3a(EUCOMM)Hmgu>	C57BL/6-Wdr62<tm3a(EUCOMM)Hmgu>	N	34059773
MGI:6758665	M	MP:0001147	small testis	Wdr62<tm3a(EUCOMM)Hmgu>/Wdr62<tm3a(EUCOMM)Hmgu>	C57BL/6-Wdr62<tm3a(EUCOMM)Hmgu>	N	34059773
MGI:6758665	M	MP:0009230	abnormal sperm head morphology	Wdr62<tm3a(EUCOMM)Hmgu>/Wdr62<tm3a(EUCOMM)Hmgu>	C57BL/6-Wdr62<tm3a(EUCOMM)Hmgu>	N	34059773
MGI:6758665	M	MP:0031375	abnormal manchette disassembly	Wdr62<tm3a(EUCOMM)Hmgu>/Wdr62<tm3a(EUCOMM)Hmgu>	C57BL/6-Wdr62<tm3a(EUCOMM)Hmgu>	N	34059773
MGI:6758665	F	MP:0001926	female infertility	Wdr62<tm3a(EUCOMM)Hmgu>/Wdr62<tm3a(EUCOMM)Hmgu>	C57BL/6-Wdr62<tm3a(EUCOMM)Hmgu>	N	34059773
MGI:6758665	M	MP:0001925	male infertility	Wdr62<tm3a(EUCOMM)Hmgu>/Wdr62<tm3a(EUCOMM)Hmgu>	C57BL/6-Wdr62<tm3a(EUCOMM)Hmgu>	N	34059773
MGI:6758665	M	MP:0002687	oligozoospermia	Wdr62<tm3a(EUCOMM)Hmgu>/Wdr62<tm3a(EUCOMM)Hmgu>	C57BL/6-Wdr62<tm3a(EUCOMM)Hmgu>	N	34059773
MGI:6759008	M	MP:0031417	decreased cardiac muscle triglyceride level	Plin5<tm1Macl>/Plin5<tm1Macl>	involves: 129S6/SvEvTac * C57BL/6JBomTac	N	27376234
MGI:6759008	M	MP:0000266	abnormal heart morphology	Plin5<tm1Macl>/Plin5<tm1Macl>	involves: 129S6/SvEvTac * C57BL/6JBomTac	N	27376234
MGI:6759008	M	MP:0000343	abnormal response to cardiac infarction	Plin5<tm1Macl>/Plin5<tm1Macl>	involves: 129S6/SvEvTac * C57BL/6JBomTac	N	27376234
MGI:6759008	M	MP:0030018	increased cardiac muscle cell glucose uptake	Plin5<tm1Macl>/Plin5<tm1Macl>	involves: 129S6/SvEvTac * C57BL/6JBomTac	N	27376234
MGI:6759008	M	MP:0014172	decreased fatty acid oxidation	Plin5<tm1Macl>/Plin5<tm1Macl>	involves: 129S6/SvEvTac * C57BL/6JBomTac	N	27376234
MGI:6759008	M	MP:0001544	abnormal cardiovascular system physiology	Plin5<tm1Macl>/Plin5<tm1Macl>	involves: 129S6/SvEvTac * C57BL/6JBomTac	N	27376234
MGI:6759016	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Zfp541<em1Osb>/Zfp541<em1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/0	involves: 129S2/SvPas * C57BL/6NSlc	N	33961623
MGI:6759016	M	MP:0001925	male infertility	Zfp541<em1Osb>/Zfp541<em1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/0	involves: 129S2/SvPas * C57BL/6NSlc	N	33961623
MGI:6759016	M	MP:0006380	abnormal spermatid morphology	Zfp541<em1Osb>/Zfp541<em1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/0	involves: 129S2/SvPas * C57BL/6NSlc	N	33961623
MGI:6759016	M	MP:0009452	abnormal synaptonemal complex	Zfp541<em1Osb>/Zfp541<em1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/0	involves: 129S2/SvPas * C57BL/6NSlc	N	33961623
MGI:6759016	M	MP:0008261	arrest of male meiosis	Zfp541<em1Osb>/Zfp541<em1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/0	involves: 129S2/SvPas * C57BL/6NSlc	N	33961623
MGI:6759016	M	MP:0030935	increased primordial germ cell apoptosis	Zfp541<em1Osb>/Zfp541<em1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/0	involves: 129S2/SvPas * C57BL/6NSlc	N	33961623
MGI:6759016	M	MP:0005169	abnormal male meiosis	Zfp541<em1Osb>/Zfp541<em1Osb>,Tg(CAG-EGFP,Acr-EGFP)2Osb/0	involves: 129S2/SvPas * C57BL/6NSlc	N	33961623
MGI:6759017	M	MP:0004852	decreased testis weight	Kctd19<em1Osb>/Kctd19<em1Osb>	Not Specified	N	33961623
MGI:6759017	M	MP:0001925	male infertility	Kctd19<em1Osb>/Kctd19<em1Osb>	Not Specified	N	33961623
MGI:6759017	M	MP:0005159	azoospermia	Kctd19<em1Osb>/Kctd19<em1Osb>	Not Specified	N	33961623
MGI:6759017	M	MP:0006380	abnormal spermatid morphology	Kctd19<em1Osb>/Kctd19<em1Osb>	Not Specified	N	33961623
MGI:6759017	M	MP:0030935	increased primordial germ cell apoptosis	Kctd19<em1Osb>/Kctd19<em1Osb>	Not Specified	N	33961623
MGI:6759017	M	MP:0005169	abnormal male meiosis	Kctd19<em1Osb>/Kctd19<em1Osb>	Not Specified	N	33961623
MGI:6759017	F	MP:0005389	reproductive system phenotype	Kctd19<em1Osb>/Kctd19<em1Osb>	Not Specified	Y	33961623
MGI:6759017	M	MP:0008261	arrest of male meiosis	Kctd19<em1Osb>/Kctd19<em1Osb>	Not Specified	N	33961623
MGI:6759017	M	MP:0009452	abnormal synaptonemal complex	Kctd19<em1Osb>/Kctd19<em1Osb>	Not Specified	N	33961623
MGI:6759019	F	MP:0005389	reproductive system phenotype	Kctd19<em2Osb>/Kctd19<em2Osb>	Not Specified	Y	33961623
MGI:6759019	M	MP:0001925	male infertility	Kctd19<em2Osb>/Kctd19<em2Osb>	Not Specified	N	33961623
MGI:6759020	M	MP:0005389	reproductive system phenotype	Kctd19<em1Osb>/Kctd19<em1Osb>,Tg(Clgn-Kctd19)HAOsb/0	Not Specified	Y	33961623
MGI:6759022	M	MP:0005389	reproductive system phenotype	Kctd19<em1Osb>/Kctd19<em1Osb>,Tg(Clgn-Kctd19)FLAGOsb/0,Tg(Clgn-Kctd19)HAOsb/0	Not Specified	Y	33961623
MGI:6760664	F	MP:0001126	abnormal ovary morphology	Syce1<em1Rrca>/Syce1<em1Rrca>	involves: C57BL/6J	N	32402064
MGI:6760664	M	MP:0001147	small testis	Syce1<em1Rrca>/Syce1<em1Rrca>	involves: C57BL/6J	N	32402064
MGI:6760664	M	MP:0005159	azoospermia	Syce1<em1Rrca>/Syce1<em1Rrca>	involves: C57BL/6J	N	32402064
MGI:6760664	F	MP:0002777	absent ovarian follicles	Syce1<em1Rrca>/Syce1<em1Rrca>	involves: C57BL/6J	N	32402064
MGI:6760664	F	MP:0001127	small ovary	Syce1<em1Rrca>/Syce1<em1Rrca>	involves: C57BL/6J	N	32402064
MGI:6760664	F	MP:0004805	absent oocytes	Syce1<em1Rrca>/Syce1<em1Rrca>	involves: C57BL/6J	N	32402064
MGI:6760664	M	MP:0001156	abnormal spermatogenesis	Syce1<em1Rrca>/Syce1<em1Rrca>	involves: C57BL/6J	N	32402064
MGI:6760664	M	MP:0008261	arrest of male meiosis	Syce1<em1Rrca>/Syce1<em1Rrca>	involves: C57BL/6J	N	32402064
MGI:6760664	M	MP:0001153	small seminiferous tubules	Syce1<em1Rrca>/Syce1<em1Rrca>	involves: C57BL/6J	N	32402064
MGI:6761753	M	MP:0009232	abnormal sperm nucleus morphology	Tent5c<em1Hncs>/Tent5c<em1Hncs>	involves: C57BL/6J * DBA	N	31087039
MGI:6761753	M	MP:0002687	oligozoospermia	Tent5c<em1Hncs>/Tent5c<em1Hncs>	involves: C57BL/6J * DBA	N	31087039
MGI:6761753	M	MP:0009830	abnormal sperm connecting piece morphology	Tent5c<em1Hncs>/Tent5c<em1Hncs>	involves: C57BL/6J * DBA	N	31087039
MGI:6761753	M	MP:0009234	absent sperm head	Tent5c<em1Hncs>/Tent5c<em1Hncs>	involves: C57BL/6J * DBA	N	31087039
MGI:6761753	M	MP:0001925	male infertility	Tent5c<em1Hncs>/Tent5c<em1Hncs>	involves: C57BL/6J * DBA	N	31087039
MGI:6761763	M	MP:0001922	reduced male fertility	Rps21<em1Utr>/Rps21<+>	Not Specified	N	33949947
MGI:6761768	F	MP:0005431	decreased oocyte number	Rnf114<em1Nju>/Rnf114<em1Nju>	involves: C57BL/6J * DBA/2J	N	34104941
MGI:6761768	M	MP:0005389	reproductive system phenotype	Rnf114<em1Nju>/Rnf114<em1Nju>	involves: C57BL/6J * DBA/2J	Y	34104941
MGI:6761768	F	MP:0003718	maternal effect	Rnf114<em1Nju>/Rnf114<em1Nju>	involves: C57BL/6J * DBA/2J	N	34104941
MGI:6761768	F	MP:0001926	female infertility	Rnf114<em1Nju>/Rnf114<em1Nju>	involves: C57BL/6J * DBA/2J	N	34104941
MGI:6764568	M	MP:0008261	arrest of male meiosis	Majin<em1Smtb>/Majin<em1Smtb>	C57BL/6NSlc-Majin<em1Smtb>/Smtb	N	34326397
MGI:6764568	F	MP:0004805	absent oocytes	Majin<em1Smtb>/Majin<em1Smtb>	C57BL/6NSlc-Majin<em1Smtb>/Smtb	N	34326397
MGI:6764568	M	MP:0001147	small testis	Majin<em1Smtb>/Majin<em1Smtb>	C57BL/6NSlc-Majin<em1Smtb>/Smtb	N	34326397
MGI:6764568	M	MP:0005159	azoospermia	Majin<em1Smtb>/Majin<em1Smtb>	C57BL/6NSlc-Majin<em1Smtb>/Smtb	N	34326397
MGI:6764570	F	MP:0004805	absent oocytes	Majin<em2Smtb>/Majin<em2Smtb>	C57BL/6NSlc-Majin<em2Smtb>/Smtb	N	34326397
MGI:6764570	M	MP:0001147	small testis	Majin<em2Smtb>/Majin<em2Smtb>	C57BL/6NSlc-Majin<em2Smtb>/Smtb	N	34326397
MGI:6764570	M	MP:0005159	azoospermia	Majin<em2Smtb>/Majin<em2Smtb>	C57BL/6NSlc-Majin<em2Smtb>/Smtb	N	34326397
MGI:6764570	M	MP:0008261	arrest of male meiosis	Majin<em2Smtb>/Majin<em2Smtb>	C57BL/6NSlc-Majin<em2Smtb>/Smtb	N	34326397
MGI:6764572	M	MP:0005389	reproductive system phenotype	Faiml<em1Smtb>/Faiml<em1Smtb>	C57BL/6NSlc-Faiml<em1Smtb>/Smtb	Y	34326397
MGI:6764572	M	MP:0001147	small testis	Faiml<em1Smtb>/Faiml<em1Smtb>	C57BL/6NSlc-Faiml<em1Smtb>/Smtb	N	34326397
MGI:6764574	M	MP:0005389	reproductive system phenotype	Cox8c<em1Smtb>/Cox8c<em1Smtb>	C57BL/6NSlc-Cox8c<em1Smtb>/Smtb	Y	34326397
MGI:6764577	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Cox7b2<em1Smtb>/Cox7b2<em1Smtb>	C57BL/6NSlc-Cox7b2<em1Smtb>/Smtb	N	34326397
MGI:6764577	M	MP:0001925	male infertility	Cox7b2<em1Smtb>/Cox7b2<em1Smtb>	C57BL/6NSlc-Cox7b2<em1Smtb>/Smtb	N	34326397
MGI:6764577	M	MP:0002675	asthenozoospermia	Cox7b2<em1Smtb>/Cox7b2<em1Smtb>	C57BL/6NSlc-Cox7b2<em1Smtb>/Smtb	N	34326397
MGI:6764577	M	MP:0000242	impaired fertilization	Cox7b2<em1Smtb>/Cox7b2<em1Smtb>	C57BL/6NSlc-Cox7b2<em1Smtb>/Smtb	N	34326397
MGI:6764577	M	MP:0005578	teratozoospermia	Cox7b2<em1Smtb>/Cox7b2<em1Smtb>	C57BL/6NSlc-Cox7b2<em1Smtb>/Smtb	N	34326397
MGI:6764577	M	MP:0009831	abnormal sperm midpiece morphology	Cox7b2<em1Smtb>/Cox7b2<em1Smtb>	C57BL/6NSlc-Cox7b2<em1Smtb>/Smtb	N	34326397
MGI:6764577	M	MP:0005389	reproductive system phenotype	Cox7b2<em1Smtb>/Cox7b2<em1Smtb>	C57BL/6NSlc-Cox7b2<em1Smtb>/Smtb	Y	34326397
MGI:6764577	M	MP:0009230	abnormal sperm head morphology	Cox7b2<em1Smtb>/Cox7b2<em1Smtb>	C57BL/6NSlc-Cox7b2<em1Smtb>/Smtb	N	34326397
MGI:6764579	M	MP:0030976	impaired sperm penetration of zona pellucida	Gm773<em1Smtb>/Y	C57BL/6NSlc-Gm773<em1Smtb>/Smtb	N	34326397
MGI:6764579	M	MP:0001922	reduced male fertility	Gm773<em1Smtb>/Y	C57BL/6NSlc-Gm773<em1Smtb>/Smtb	N	34326397
MGI:6764579	M	MP:0005389	reproductive system phenotype	Gm773<em1Smtb>/Y	C57BL/6NSlc-Gm773<em1Smtb>/Smtb	Y	34326397
MGI:6764585	M	MP:0001922	reduced male fertility	Tuba3a<em2Smtb>/Tuba3a<em2Smtb>,Tuba3b<em2Smtb>/Tuba3b<em2Smtb>	C57BL/6NSlc-Tuba3a<em2Smtb> Tuba3b<em2Smtb>/Smtb	N	34326397
MGI:6764585	M	MP:0005389	reproductive system phenotype	Tuba3a<em2Smtb>/Tuba3a<em2Smtb>,Tuba3b<em2Smtb>/Tuba3b<em2Smtb>	C57BL/6NSlc-Tuba3a<em2Smtb> Tuba3b<em2Smtb>/Smtb	Y	34326397
MGI:6764585	M	MP:0030976	impaired sperm penetration of zona pellucida	Tuba3a<em2Smtb>/Tuba3a<em2Smtb>,Tuba3b<em2Smtb>/Tuba3b<em2Smtb>	C57BL/6NSlc-Tuba3a<em2Smtb> Tuba3b<em2Smtb>/Smtb	N	34326397
MGI:6765292	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Bcorl1<em1Nju>/Y	C57BL/6J-Bcorl1<em1Nju>	N	32376790
MGI:6765292	M	MP:0001156	abnormal spermatogenesis	Bcorl1<em1Nju>/Y	C57BL/6J-Bcorl1<em1Nju>	N	32376790
MGI:6765292	M	MP:0002687	oligozoospermia	Bcorl1<em1Nju>/Y	C57BL/6J-Bcorl1<em1Nju>	N	32376790
MGI:6765292	M	MP:0004852	decreased testis weight	Bcorl1<em1Nju>/Y	C57BL/6J-Bcorl1<em1Nju>	N	32376790
MGI:6765292	M	MP:0001925	male infertility	Bcorl1<em1Nju>/Y	C57BL/6J-Bcorl1<em1Nju>	N	32376790
MGI:6765452	M	MP:0001922	reduced male fertility	Actrt1<em1Xwei>/Y	C57BL/6-Actrt1<em1Xwei>	N	34422805
MGI:6765452	M	MP:0009234	absent sperm head	Actrt1<em1Xwei>/Y	C57BL/6-Actrt1<em1Xwei>	N	34422805
MGI:6765452	M	MP:0006380	abnormal spermatid morphology	Actrt1<em1Xwei>/Y	C57BL/6-Actrt1<em1Xwei>	N	34422805
MGI:6765943	F	MP:0031213	increased eye anterior chamber depth	Zfp469<em1Chms>/Zfp469<em1Chms>	C57BL/6J-Zfp469<em1Chms>	N	34368841
MGI:6765943	F	MP:0002750	exophthalmos	Zfp469<em1Chms>/Zfp469<em1Chms>	C57BL/6J-Zfp469<em1Chms>	N	34368841
MGI:6771321	M	MP:0031009	abnormal sperm-egg fusion	Spaca4<em2Pauli>/Spaca4<em2Pauli>	C57BL/6J-Spaca4<em2Pauli>/Osb	N	34556579
MGI:6771323	F	MP:0005389	reproductive system phenotype	Spaca4<em1Pauli>/Spaca4<em2Pauli>	C57BL/6J-Spaca4<em1Pauli>/Spaca4<em2Pauli>	Y	34556579
MGI:6771323	M	MP:0001935	decreased litter size	Spaca4<em1Pauli>/Spaca4<em2Pauli>	C57BL/6J-Spaca4<em1Pauli>/Spaca4<em2Pauli>	N	34556579
MGI:6771323	M	MP:0031009	abnormal sperm-egg fusion	Spaca4<em1Pauli>/Spaca4<em2Pauli>	C57BL/6J-Spaca4<em1Pauli>/Spaca4<em2Pauli>	N	34556579
MGI:6771323	M	MP:0002675	asthenozoospermia	Spaca4<em1Pauli>/Spaca4<em2Pauli>	C57BL/6J-Spaca4<em1Pauli>/Spaca4<em2Pauli>	N	34556579
MGI:6771323	M	MP:0001922	reduced male fertility	Spaca4<em1Pauli>/Spaca4<em2Pauli>	C57BL/6J-Spaca4<em1Pauli>/Spaca4<em2Pauli>	N	34556579
MGI:6771323	M	MP:0009647	decreased fertilization frequency	Spaca4<em1Pauli>/Spaca4<em2Pauli>	C57BL/6J-Spaca4<em1Pauli>/Spaca4<em2Pauli>	N	34556579
MGI:6771328	M	MP:0009647	decreased fertilization frequency	Spaca4<tm1Osb>/Spaca4<tm1Osb>	involves: C57BL/6NSlc * DBA	N	34556579
MGI:6771328	M	MP:0002675	asthenozoospermia	Spaca4<tm1Osb>/Spaca4<tm1Osb>	involves: C57BL/6NSlc * DBA	N	34556579
MGI:6771593	M	MP:0005389	reproductive system phenotype	Pbk<em1Sdgl>/Pbk<em1Sdgl>	C57BL/6-Pbk<em1Sdgl>	Y	32586419
MGI:6771595	M	MP:0005389	reproductive system phenotype	Pbk<em2Sdgl>/Pbk<em2Sdgl>	C57BL/6-Pbk<em2Sdgl>	N	32586419
MGI:6771930	M	MP:0001399	hyperactivity	Aacs<em1(IMPC)J>/Aacs<em1(IMPC)J>	C57BL/6NJ-Aacs<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771931	M	MP:0005016	decreased lymphocyte cell number	Abcc9<em1(IMPC)H>/Abcc9<+>	C57BL/6N-Abcc9<em1(IMPC)H>/H	N	MGI:5576271
MGI:6771931	F	MP:0010052	increased grip strength	Abcc9<em1(IMPC)H>/Abcc9<+>	C57BL/6N-Abcc9<em1(IMPC)H>/H	N	MGI:5576271
MGI:6771931	M	MP:0000219	increased neutrophil cell number	Abcc9<em1(IMPC)H>/Abcc9<+>	C57BL/6N-Abcc9<em1(IMPC)H>/H	N	MGI:5576271
MGI:6771932	F	MP:0001417	decreased exploration in new environment	Abhd4<em1(IMPC)J>/Abhd4<em1(IMPC)J>	C57BL/6NJ-Abhd4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771933	M	MP:0010052	increased grip strength	Acnat2<em1(IMPC)Hmgu>/Acnat2<+>	C57BL/6N-Acnat2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6771934	F	MP:0001556	increased circulating HDL cholesterol level	Adcy2<tm1a(KOMP)Wtsi>/Adcy2<tm1a(KOMP)Wtsi>	C57BL/6N-Adcy2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6771935	M	MP:0020421	increased freezing behavior	Adprhl1<em1(IMPC)H>/Adprhl1<em1(IMPC)H>	C57BL/6NTac-Adprhl1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6771936	F	MP:0020421	increased freezing behavior	Agbl4<em1(IMPC)Mbp>/Agbl4<+>	C57BL/6NCrl-Agbl4<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:6771937	F	MP:0010053	decreased grip strength	Ak3<em1(IMPC)J>/Ak3<em1(IMPC)J>	C57BL/6NJ-Ak3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771938	F	MP:0000367	abnormal coat/ hair morphology	Akap8l<em1(IMPC)J>/Akap8l<em1(IMPC)J>	C57BL/6NJ-Akap8l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771938	M	MP:0003179	thrombocytopenia	Akap8l<em1(IMPC)J>/Akap8l<em1(IMPC)J>	C57BL/6NJ-Akap8l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771938	F	MP:0002941	increased circulating alanine transaminase level	Akap8l<em1(IMPC)J>/Akap8l<em1(IMPC)J>	C57BL/6NJ-Akap8l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771939	F	MP:0010052	increased grip strength	Amigo2<em1(IMPC)J>/Amigo2<em1(IMPC)J>	C57BL/6NJ-Amigo2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771940	M	MP:0001417	decreased exploration in new environment	Ankrd65<tm1(KOMP)Wtsi>/Ankrd65<tm1(KOMP)Wtsi>	C57BL/6N-Ankrd65<tm1(KOMP)Wtsi>/Mhzh	N	MGI:5576271
MGI:6771941	F	MP:0002953	thick ventricular wall	Ap3m2<em2(IMPC)H>/Ap3m2<em2(IMPC)H>	C57BL/6NTac-Ap3m2<em2(IMPC)H>/H	N	MGI:5576271
MGI:6771942	M	MP:0002764	short tibia	Arl15<em1(IMPC)H>/Arl15<+>	C57BL/6N-Arl15<em1(IMPC)H>/H	N	MGI:5576271
MGI:6771942	F	MP:0005553	increased circulating creatinine level	Arl15<em1(IMPC)H>/Arl15<+>	C57BL/6N-Arl15<em1(IMPC)H>/H	N	MGI:5576271
MGI:6771943	M	MP:0010067	increased red blood cell distribution width	Art4<tm1a(KOMP)Wtsi>/Art4<tm1a(KOMP)Wtsi>	C57BL/6N-Art4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6771945	F	MP:0000208	decreased hematocrit	Trem6l<tm1b(KOMP)Wtsi>/Trem6l<tm1b(KOMP)Wtsi>	C57BL/6N-Trem6l<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6771945	F	MP:0002874	decreased hemoglobin content	Trem6l<tm1b(KOMP)Wtsi>/Trem6l<tm1b(KOMP)Wtsi>	C57BL/6N-Trem6l<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6771946	F	MP:0002874	decreased hemoglobin content	BC049715<tm1b(KOMP)Mbp>/BC049715<tm1b(KOMP)Mbp>	C57BL/6N-BC049715<tm1b(KOMP)Mbp>/Mhzh	N	MGI:5576271
MGI:6771946	F	MP:0000208	decreased hematocrit	BC049715<tm1b(KOMP)Mbp>/BC049715<tm1b(KOMP)Mbp>	C57BL/6N-BC049715<tm1b(KOMP)Mbp>/Mhzh	N	MGI:5576271
MGI:6771946	F	MP:0002875	decreased erythrocyte cell number	BC049715<tm1b(KOMP)Mbp>/BC049715<tm1b(KOMP)Mbp>	C57BL/6N-BC049715<tm1b(KOMP)Mbp>/Mhzh	N	MGI:5576271
MGI:6771948	M	MP:0001417	decreased exploration in new environment	Bnip1<tm2b(KOMP)Wtsi>/Bnip1<+>	C57BL/6N-Bnip1<tm2b(KOMP)Wtsi>/Nju	N	MGI:5576271
MGI:6771949	M	MP:0005553	increased circulating creatinine level	Bpgm<tm1a(KOMP)Wtsi>/Bpgm<tm1a(KOMP)Wtsi>	C57BL/6N-Bpgm<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6771950	F	MP:0005505	thrombocytosis	Brcc3<em1(IMPC)Wtsi>/Brcc3<em1(IMPC)Wtsi>	C57BL/6N-Brcc3<em1(IMPC)Wtsi>/WtsiCnrm	N	MGI:5576271
MGI:6771951	M	MP:0005343	increased circulating aspartate transaminase level	C1qtnf3<tm2b(EUCOMM)Wtsi>/C1qtnf3<tm2b(EUCOMM)Wtsi>	C57BL/6N-C1qtnf3<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6771951	M	MP:0010090	increased circulating creatine kinase level	C1qtnf3<tm2b(EUCOMM)Wtsi>/C1qtnf3<tm2b(EUCOMM)Wtsi>	C57BL/6N-C1qtnf3<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6771951	M	MP:0002941	increased circulating alanine transaminase level	C1qtnf3<tm2b(EUCOMM)Wtsi>/C1qtnf3<tm2b(EUCOMM)Wtsi>	C57BL/6N-C1qtnf3<tm2b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6771952	M	MP:0003896	prolonged PR interval	Cbl<tm1b(EUCOMM)Hmgu>/Cbl<+>	C57BL/6N-Cbl<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6771953	M	MP:0008806	increased circulating amylase level	Ccdc103<em4(IMPC)H>/Ccdc103<+>	C57BL/6N-Ccdc103<em4(IMPC)H>/H	N	MGI:5576271
MGI:6771953	M	MP:0010024	increased total body fat amount	Ccdc103<em4(IMPC)H>/Ccdc103<+>	C57BL/6N-Ccdc103<em4(IMPC)H>/H	N	MGI:5576271
MGI:6771953	M	MP:0003961	decreased lean body mass	Ccdc103<em4(IMPC)H>/Ccdc103<+>	C57BL/6N-Ccdc103<em4(IMPC)H>/H	N	MGI:5576271
MGI:6771954	F	MP:0004952	increased spleen weight	Ccl17<em1(IMPC)H>/Ccl17<em1(IMPC)H>	C57BL/6N-Ccl17<em1(IMPC)H>/H	N	MGI:5576271
MGI:6771955	M	MP:0005343	increased circulating aspartate transaminase level	Cd300ld<em1(IMPC)Wtsi>/Cd300ld<em1(IMPC)Wtsi>	C57BL/6N-Cd300ld<em1(IMPC)Wtsi>/WtsiIeg	N	MGI:5576271
MGI:6771956	M	MP:0001417	decreased exploration in new environment	Cdk8<tm1b(EUCOMM)Hmgu>/Cdk8<+>	C57BL/6N-Cdk8<tm1b(EUCOMM)Hmgu>/Ics	N	MGI:5576271
MGI:6771957	M	MP:0009142	decreased prepulse inhibition	Cfap97d1<tm1b(KOMP)Wtsi>/Cfap97d1<tm1b(KOMP)Wtsi>	C57BL/6N-Cfap97d1<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6771958	M	MP:0011886	increased circulating lipase level	Chaf1b<tm1b(EUCOMM)Hmgu>/Chaf1b<+>	C57BL/6N-Chaf1b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6771958	M	MP:0008806	increased circulating amylase level	Chaf1b<tm1b(EUCOMM)Hmgu>/Chaf1b<+>	C57BL/6N-Chaf1b<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6771959	F	MP:0003019	increased circulating chloride level	Cldn34b2<tm1a(KOMP)Wtsi>/Cldn34b2<tm1a(KOMP)Wtsi>	C57BL/6N-Cldn34b2<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6771960	M	MP:0005140	decreased cardiac muscle contractility	Clec9a<tm1b(KOMP)Wtsi>/Clec9a<tm1b(KOMP)Wtsi>	C57BL/6N-Clec9a<tm1b(KOMP)Wtsi>/Orl	N	MGI:5576271
MGI:6771961	F	MP:0002968	increased circulating alkaline phosphatase level	Cmtm7<em1(IMPC)J>/Cmtm7<em1(IMPC)J>	C57BL/6NJ-Cmtm7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771962	M	MP:0005407	hyperalgesia	Cnrip1<em1(IMPC)Mbp>/Cnrip1<em1(IMPC)Mbp>	C57BL/6N-Cnrip1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6771962	M	MP:0001417	decreased exploration in new environment	Cnrip1<em1(IMPC)Mbp>/Cnrip1<em1(IMPC)Mbp>	C57BL/6N-Cnrip1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:6771966	M	MP:0002079	increased circulating insulin level	Dcx<tm1a(EUCOMM)Wtsi>/Y	C57BL/6N-Dcx<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6771966	M	MP:0005633	increased circulating sodium level	Dcx<tm1a(EUCOMM)Wtsi>/Y	C57BL/6N-Dcx<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6771966	M	MP:0003019	increased circulating chloride level	Dcx<tm1a(EUCOMM)Wtsi>/Y	C57BL/6N-Dcx<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6771967	M	MP:0010052	increased grip strength	Dhx37<em1(IMPC)J>/Dhx37<+>	C57BL/6NJ-Dhx37<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771967	F	MP:0002574	increased vertical activity	Dhx37<em1(IMPC)J>/Dhx37<+>	C57BL/6NJ-Dhx37<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771968	M	MP:0009142	decreased prepulse inhibition	Dhx58<em1(IMPC)J>/Dhx58<em1(IMPC)J>	C57BL/6NJ-Dhx58<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771970	M	MP:0001417	decreased exploration in new environment	Dlat<em1(IMPC)J>/Dlat<+>	C57BL/6NJ-Dlat<em1(IMPC)J>/J	N	MGI:5576271
MGI:6771971	M	MP:0010052	increased grip strength	Dok4<em1(IMPC)J>/Dok4<em1(IMPC)J>	C57BL/6NJ-Dok4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771972	F	MP:0001392	abnormal locomotor behavior	E130114P18Rik<em1(IMPC)J>/E130114P18Rik<em1(IMPC)J>	C57BL/6NJ-E130114P18Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771972	F	MP:0001399	hyperactivity	E130114P18Rik<em1(IMPC)J>/E130114P18Rik<em1(IMPC)J>	C57BL/6NJ-E130114P18Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771973	F	MP:0005293	impaired glucose tolerance	Eef2kmt<tm1b(EUCOMM)Wtsi>/Eef2kmt<tm1b(EUCOMM)Wtsi>	C57BL/6N-Eef2kmt<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6771974	F	MP:0001402	decreased locomotor activity	Enho<tm1.1(KOMP)Vlcg>/Enho<tm1.1(KOMP)Vlcg>	C57BL/6N-Enho<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:6771978	F	MP:0001402	decreased locomotor activity	Faxc<em1(IMPC)J>/Faxc<+>	C57BL/6NJ-Faxc<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771980	M	MP:0000182	increased circulating LDL cholesterol level	Flvcr2<tm1a(EUCOMM)Hmgu>/Flvcr2<+>	C57BL/6N-Flvcr2<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6771980	M	MP:0001556	increased circulating HDL cholesterol level	Flvcr2<tm1a(EUCOMM)Hmgu>/Flvcr2<+>	C57BL/6N-Flvcr2<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6771980	M	MP:0005178	increased circulating cholesterol level	Flvcr2<tm1a(EUCOMM)Hmgu>/Flvcr2<+>	C57BL/6N-Flvcr2<tm1a(EUCOMM)Hmgu>/Wtsi	N	MGI:5576271
MGI:6771981	F	MP:0002833	increased heart weight	Gle1<tm1a(EUCOMM)Wtsi>/Gle1<+>	C57BL/6N-Gle1<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6771983	F	MP:0010124	decreased bone mineral content	Gprasp2<em1(IMPC)J>/Gprasp2<em1(IMPC)J>	C57BL/6NJ-Gprasp2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771983	F	MP:0002968	increased circulating alkaline phosphatase level	Gprasp2<em1(IMPC)J>/Gprasp2<em1(IMPC)J>	C57BL/6NJ-Gprasp2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771987	M	MP:0005505	thrombocytosis	Igf2bp3<em1(IMPC)J>/Igf2bp3<em1(IMPC)J>	C57BL/6NJ-Igf2bp3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771987	F	MP:0010052	increased grip strength	Igf2bp3<em1(IMPC)J>/Igf2bp3<em1(IMPC)J>	C57BL/6NJ-Igf2bp3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771988	F	MP:0000208	decreased hematocrit	Inf2<tm1.1(KOMP)Vlcg>/Inf2<tm1.1(KOMP)Vlcg>	C57BL/6N-Inf2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6771989	M	MP:0001399	hyperactivity	Iqch<em1(IMPC)J>/Iqch<em1(IMPC)J>	C57BL/6NJ-Iqch<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771989	F	MP:0010053	decreased grip strength	Iqch<em1(IMPC)J>/Iqch<em1(IMPC)J>	C57BL/6NJ-Iqch<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6771990	F	MP:0002968	increased circulating alkaline phosphatase level	Irak2<tm1b(EUCOMM)Wtsi>/Irak2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Irak2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6771990	M	MP:0010024	increased total body fat amount	Irak2<tm1b(EUCOMM)Wtsi>/Irak2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Irak2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6771990	M	MP:0002764	short tibia	Irak2<tm1b(EUCOMM)Wtsi>/Irak2<tm1b(EUCOMM)Wtsi>	C57BL/6N-Irak2<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6771991	F	MP:0005011	increased eosinophil cell number	Kcnip1<em1(IMPC)H>/Kcnip1<em1(IMPC)H>	C57BL/6N-Kcnip1<em1(IMPC)H>/H	N	MGI:5576271
MGI:6771992	F	MP:0002764	short tibia	Kcnip3<tm2b(EUCOMM)Hmgu>/Kcnip3<tm2b(EUCOMM)Hmgu>	C57BL/6N-Kcnip3<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6771993	M	MP:0003179	thrombocytopenia	Kcnip4<tm1a(KOMP)Wtsi>/Kcnip4<tm1a(KOMP)Wtsi>	C57BL/6N-Kcnip4<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6771994	M	MP:0010024	increased total body fat amount	Kcnn1<tm1b(KOMP)Wtsi>/Kcnn1<tm1b(KOMP)Wtsi>	C57BL/6N-Kcnn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6771994	F	MP:0010067	increased red blood cell distribution width	Kcnn1<tm1b(KOMP)Wtsi>/Kcnn1<tm1b(KOMP)Wtsi>	C57BL/6N-Kcnn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6771994	M	MP:0000063	decreased bone mineral density	Kcnn1<tm1b(KOMP)Wtsi>/Kcnn1<tm1b(KOMP)Wtsi>	C57BL/6N-Kcnn1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6771995	M	MP:0003019	increased circulating chloride level	Kifbp<tm1a(KOMP)Wtsi>/Kifbp<+>	C57BL/6N-Kifbp<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6771998	F	MP:0000219	increased neutrophil cell number	Lage3<em1(IMPC)Tcp>/Lage3<em1(IMPC)Tcp>	C57BL/6N-Lage3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:6771999	F	MP:0003731	abnormal retina outer nuclear layer morphology	Mboat4<tm2b(EUCOMM)Hmgu>/Mboat4<tm2b(EUCOMM)Hmgu>	C57BL/6N-Mboat4<tm2b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6772000	F	MP:0003733	abnormal retina inner nuclear layer morphology	Mdh1b<em1(IMPC)Bay>/Mdh1b<em1(IMPC)Bay>	C57BL/6N-Mdh1b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6772001	M	MP:0001556	increased circulating HDL cholesterol level	Mgst1<em1(IMPC)J>/Mgst1<em1(IMPC)J>	C57BL/6NJ-Mgst1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772001	M	MP:0005178	increased circulating cholesterol level	Mgst1<em1(IMPC)J>/Mgst1<em1(IMPC)J>	C57BL/6NJ-Mgst1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772002	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Mospd1<tm1a(KOMP)Wtsi>/Y	C57BL/6N-Mospd1<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6772003	M	MP:0001399	hyperactivity	Msl3<em1(IMPC)J>/Y	C57BL/6NJ-Msl3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772005	M	MP:0011886	increased circulating lipase level	Oma1<em1(IMPC)Hmgu>/Oma1<em1(IMPC)Hmgu>	C57BL/6N-Oma1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6772007	F	MP:0001402	decreased locomotor activity	P2rx2<em1(IMPC)H>/P2rx2<em1(IMPC)H>	C57BL/6NTac-P2rx2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6772009	M	MP:0005011	increased eosinophil cell number	Pan2<tm1b(KOMP)Wtsi>/Pan2<tm1b(KOMP)Wtsi>	C57BL/6N-Pan2<tm1b(KOMP)Wtsi>/Mhzh	N	MGI:5576271
MGI:6772009	M	MP:0002833	increased heart weight	Pan2<tm1b(KOMP)Wtsi>/Pan2<tm1b(KOMP)Wtsi>	C57BL/6N-Pan2<tm1b(KOMP)Wtsi>/Mhzh	N	MGI:5576271
MGI:6772010	F	MP:0002753	dilated heart left ventricle	Pcdhgc3<em1(IMPC)Hmgu>/Pcdhgc3<em1(IMPC)Hmgu>	C57BL/6N-Pcdhgc3<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6772011	M	MP:0002941	increased circulating alanine transaminase level	Pcsk2<em1(IMPC)H>/Pcsk2<+>	C57BL/6NTac-Pcsk2<em1(IMPC)H>/H	N	MGI:5576271
MGI:6772012	M	MP:0000579	abnormal nail morphology	Pfas<em1(IMPC)J>/Pfas<+>	C57BL/6NJ-Pfas<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772012	F	MP:0000443	abnormal snout morphology	Pfas<em1(IMPC)J>/Pfas<+>	C57BL/6NJ-Pfas<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772013	F	MP:0011951	increased cardiac stroke volume	Pla2g2e<tm1b(EUCOMM)Wtsi>/Pla2g2e<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pla2g2e<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6772013	M	MP:0002968	increased circulating alkaline phosphatase level	Pla2g2e<tm1b(EUCOMM)Wtsi>/Pla2g2e<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pla2g2e<tm1b(EUCOMM)Wtsi>/Ieg	N	MGI:5576271
MGI:6772014	F	MP:0001399	hyperactivity	Plb1<em1(IMPC)J>/Plb1<em1(IMPC)J>	C57BL/6NJ-Plb1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772015	M	MP:0011886	increased circulating lipase level	Plekhh1<tm1.1(KOMP)Mbp>/Plekhh1<tm1.1(KOMP)Mbp>	C57BL/6N-Plekhh1<tm1.1(KOMP)Mbp>/Ieg	N	MGI:5576271
MGI:6772016	M	MP:0010506	prolonged RR interval	Poli<tm1b(EUCOMM)Hmgu>/Poli<tm1b(EUCOMM)Hmgu>	C57BL/6N-Poli<tm1b(EUCOMM)Hmgu>/BayMmucd	N	MGI:5576271
MGI:6772017	M	MP:0001417	decreased exploration in new environment	Ppfia4<em1(IMPC)Bay>/Ppfia4<em1(IMPC)Bay>	C57BL/6N-Ppfia4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6772017	F	MP:0011962	increased cornea thickness	Ppfia4<em1(IMPC)Bay>/Ppfia4<em1(IMPC)Bay>	C57BL/6N-Ppfia4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:6772019	M	MP:0002833	increased heart weight	Pram1<tm1b(EUCOMM)Wtsi>/Pram1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Pram1<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:6772020	M	MP:0005553	increased circulating creatinine level	Psg25<em1(IMPC)Wtsi>/Psg25<em1(IMPC)Wtsi>	C57BL/6N-Psg25<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6772020	M	MP:0005565	increased blood urea nitrogen level	Psg25<em1(IMPC)Wtsi>/Psg25<em1(IMPC)Wtsi>	C57BL/6N-Psg25<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6772021	F	MP:0005343	increased circulating aspartate transaminase level	Rab33b<em1(IMPC)J>/Rab33b<em1(IMPC)J>	C57BL/6NJ-Rab33b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772021	M	MP:0003896	prolonged PR interval	Rab33b<em1(IMPC)J>/Rab33b<em1(IMPC)J>	C57BL/6NJ-Rab33b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772021	F	MP:0005179	decreased circulating cholesterol level	Rab33b<em1(IMPC)J>/Rab33b<em1(IMPC)J>	C57BL/6NJ-Rab33b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772022	M	MP:0002574	increased vertical activity	Rasgef1a<em1(IMPC)J>/Rasgef1a<em1(IMPC)J>	C57BL/6NJ-Rasgef1a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772023	M	MP:0010053	decreased grip strength	Raver2<em1(IMPC)J>/Raver2<em1(IMPC)J>	C57BL/6NJ-Raver2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772023	M	MP:0000198	decreased circulating phosphate level	Raver2<em1(IMPC)J>/Raver2<em1(IMPC)J>	C57BL/6NJ-Raver2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772025	M	MP:0002599	increased mean platelet volume	Rnf114<em1(IMPC)Wtsi>/Rnf114<em1(IMPC)Wtsi>	C57BL/6N-Rnf114<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6772026	M	MP:0008806	increased circulating amylase level	Rnf145<em1(IMPC)Wtsi>/Rnf145<+>	C57BL/6N-Rnf145<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6772029	F	MP:0001488	increased startle reflex	Sec61a2<em1(IMPC)J>/Sec61a2<em1(IMPC)J>	C57BL/6NJ-Sec61a2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772029	M	MP:0001566	increased circulating phosphate level	Sec61a2<em1(IMPC)J>/Sec61a2<em1(IMPC)J>	C57BL/6NJ-Sec61a2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772031	M	MP:0001399	hyperactivity	Sigmar1<tm1.1(KOMP)Wtsi>/Sigmar1<tm1.1(KOMP)Wtsi>	C57BL/6N-Sigmar1<tm1.1(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:6772032	F	MP:0005575	increased pulmonary ventilation	Slc13a3<tm1b(KOMP)Wtsi>/Slc13a3<tm1b(KOMP)Wtsi>	C57BL/6N-Slc13a3<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:6772033	M	MP:0002833	increased heart weight	Slc45a3<tm1.1(KOMP)Vlcg>/Slc45a3<tm1.1(KOMP)Vlcg>	C57BL/6N-Slc45a3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:6772034	F	MP:0011886	increased circulating lipase level	Slc6a15<em1(IMPC)Hmgu>/Slc6a15<em1(IMPC)Hmgu>	C57BL/6N-Slc6a15<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6772035	M	MP:0001402	decreased locomotor activity	Slit1<tm1b(KOMP)Wtsi>/Slit1<tm1b(KOMP)Wtsi>	C57BL/6N-Slit1<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:6772038	M	MP:0002599	increased mean platelet volume	Ssc5d<em1(IMPC)Wtsi>/Ssc5d<em1(IMPC)Wtsi>	C57BL/6N-Ssc5d<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6772040	F	MP:0010025	decreased total body fat amount	Syne2<em1(IMPC)J>/Syne2<em1(IMPC)J>	C57BL/6N-Syne2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6772040	F	MP:0003960	increased lean body mass	Syne2<em1(IMPC)J>/Syne2<em1(IMPC)J>	C57BL/6N-Syne2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6772040	F	MP:0010052	increased grip strength	Syne2<em1(IMPC)J>/Syne2<em1(IMPC)J>	C57BL/6N-Syne2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6772040	F	MP:0001392	abnormal locomotor behavior	Syne2<em1(IMPC)J>/Syne2<em1(IMPC)J>	C57BL/6N-Syne2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6772040	M	MP:0002591	decreased mean corpuscular volume	Syne2<em1(IMPC)J>/Syne2<em1(IMPC)J>	C57BL/6N-Syne2<em1(IMPC)J>/J	N	MGI:5576271
MGI:6772041	M	MP:0001552	increased circulating triglyceride level	Syne3<tm1b(KOMP)Wtsi>/Syne3<tm1b(KOMP)Wtsi>	C57BL/6N-Syne3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6772041	F	MP:0005560	decreased circulating glucose level	Syne3<tm1b(KOMP)Wtsi>/Syne3<tm1b(KOMP)Wtsi>	C57BL/6N-Syne3<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:6772042	M	MP:0005344	increased circulating bilirubin level	Tax1bp3<tm1b(EUCOMM)Hmgu>/Tax1bp3<+>	C57BL/6N-Tax1bp3<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6772043	F	MP:0001284	absent vibrissae	Tecrl<em1(IMPC)J>/Tecrl<em1(IMPC)J>	C57BL/6NJ-Tecrl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772043	F	MP:0010052	increased grip strength	Tecrl<em1(IMPC)J>/Tecrl<em1(IMPC)J>	C57BL/6NJ-Tecrl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772044	M	MP:0010067	increased red blood cell distribution width	Tkt<em1(IMPC)H>/Tkt<+>	C57BL/6NTac-Tkt<em1(IMPC)H>/H	N	MGI:5576271
MGI:6772045	M	MP:0004122	abnormal sinus arrhythmia	Tlr13<tm1.1(KOMP)Vlcg>/Y	C57BL/6N-Tlr13<tm1.1(KOMP)Vlcg>/Ieg	N	MGI:5576271
MGI:6772046	F	MP:0001417	decreased exploration in new environment	Tlr13<tm1.1(KOMP)Vlcg>/Tlr13<tm1.1(KOMP)Vlcg>	C57BL/6N-Tlr13<tm1.1(KOMP)Vlcg>/Ieg	N	MGI:5576271
MGI:6772047	M	MP:0005344	increased circulating bilirubin level	Tmem37<tm1a(EUCOMM)Wtsi>/Tmem37<tm1a(EUCOMM)Wtsi>	C57BL/6N-Tmem37<tm1a(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:6772048	F	MP:0001415	increased exploration in new environment	Tmem67<em1(IMPC)J>/Tmem67<+>	C57BL/6NJ-Tmem67<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772048	F	MP:0010052	increased grip strength	Tmem67<em1(IMPC)J>/Tmem67<+>	C57BL/6NJ-Tmem67<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772049	M	MP:0005011	increased eosinophil cell number	Treh<em1(IMPC)H>/Treh<em1(IMPC)H>	C57BL/6N-Treh<em1(IMPC)H>/H	N	MGI:5576271
MGI:6772050	F	MP:0010052	increased grip strength	Tsen54<em1(IMPC)J>/Tsen54<+>	C57BL/6NJ-Tsen54<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772051	F	MP:0008810	increased circulating iron level	Tspan17<em1(IMPC)H>/Tspan17<em1(IMPC)H>	C57BL/6N-Tspan17<em1(IMPC)H>/H	N	MGI:5576271
MGI:6772052	M	MP:0005016	decreased lymphocyte cell number	Tti2<tm1b(KOMP)Wtsi>/Tti2<+>	C57BL/6N-Tti2<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6772052	M	MP:0000219	increased neutrophil cell number	Tti2<tm1b(KOMP)Wtsi>/Tti2<+>	C57BL/6N-Tti2<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6772052	M	MP:0001417	decreased exploration in new environment	Tti2<tm1b(KOMP)Wtsi>/Tti2<+>	C57BL/6N-Tti2<tm1b(KOMP)Wtsi>/Ics	N	MGI:5576271
MGI:6772053	M	MP:0010053	decreased grip strength	Ubash3a<tm1a(KOMP)Wtsi>/Ubash3a<tm1a(KOMP)Wtsi>	C57BL/6N-Ubash3a<tm1a(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:6772054	M	MP:0001488	increased startle reflex	Ube2h<tm1b(EUCOMM)Hmgu>/Ube2h<+>	C57BL/6N-Ube2h<tm1b(EUCOMM)Hmgu>/Nju	N	MGI:5576271
MGI:6772057	F	MP:0005561	increased mean corpuscular hemoglobin	Usp37<em1(IMPC)Wtsi>/Usp37<+>	C57BL/6N-Usp37<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6772058	F	MP:0000063	decreased bone mineral density	Usp51<em1(IMPC)Wtsi>/Usp51<em1(IMPC)Wtsi>	C57BL/6N-Usp51<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:6772059	M	MP:0011886	increased circulating lipase level	Zc3h12a<tm1b(EUCOMM)Hmgu>/Zc3h12a<+>	C57BL/6N-Zc3h12a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6772059	F	MP:0001566	increased circulating phosphate level	Zc3h12a<tm1b(EUCOMM)Hmgu>/Zc3h12a<+>	C57BL/6N-Zc3h12a<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:6772060	M	MP:0000220	increased monocyte cell number	Zc3h12d<tm1b(EUCOMM)Hmgu>/Zc3h12d<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zc3h12d<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6772060	M	MP:0000219	increased neutrophil cell number	Zc3h12d<tm1b(EUCOMM)Hmgu>/Zc3h12d<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zc3h12d<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6772060	M	MP:0002941	increased circulating alanine transaminase level	Zc3h12d<tm1b(EUCOMM)Hmgu>/Zc3h12d<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zc3h12d<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6772060	M	MP:0005016	decreased lymphocyte cell number	Zc3h12d<tm1b(EUCOMM)Hmgu>/Zc3h12d<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zc3h12d<tm1b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:6772061	M	MP:0002591	decreased mean corpuscular volume	Zc3h7a<em1(IMPC)J>/Zc3h7a<em1(IMPC)J>	C57BL/6NJ-Zc3h7a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772061	F	MP:0001399	hyperactivity	Zc3h7a<em1(IMPC)J>/Zc3h7a<em1(IMPC)J>	C57BL/6NJ-Zc3h7a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772061	M	MP:0005562	decreased mean corpuscular hemoglobin	Zc3h7a<em1(IMPC)J>/Zc3h7a<em1(IMPC)J>	C57BL/6NJ-Zc3h7a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772061	F	MP:0002075	abnormal coat/hair pigmentation	Zc3h7a<em1(IMPC)J>/Zc3h7a<em1(IMPC)J>	C57BL/6NJ-Zc3h7a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772061	M	MP:0020870	decreased thigmotaxis	Zc3h7a<em1(IMPC)J>/Zc3h7a<em1(IMPC)J>	C57BL/6NJ-Zc3h7a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772061	F	MP:0001529	abnormal vocalization	Zc3h7a<em1(IMPC)J>/Zc3h7a<em1(IMPC)J>	C57BL/6NJ-Zc3h7a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:6772062	F	MP:0000280	thin ventricular wall	Zmym6<em1(IMPC)Hmgu>/Zmym6<em1(IMPC)Hmgu>	C57BL/6N-Zmym6<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:6780078	M	MP:0005376	homeostasis/metabolism phenotype	Stbd1<tm1Bsn>/Stbd1<tm1Bsn>	B6.Cg-Stbd1<tm1Bsn>	Y	27358407
MGI:6780079	M	MP:0014071	increased cardiac muscle glycogen level	Gaa<tm1Rabn>/Gaa<tm1Rabn>,Stbd1<tm1Bsn>/Stbd1<tm1Bsn>	involves: 129X1/SvJ * C57BL/6	N	27358407
MGI:6780079	M	MP:0005376	homeostasis/metabolism phenotype	Gaa<tm1Rabn>/Gaa<tm1Rabn>,Stbd1<tm1Bsn>/Stbd1<tm1Bsn>	involves: 129X1/SvJ * C57BL/6	Y	27358407
MGI:6780079	M	MP:0010400	increased liver glycogen level	Gaa<tm1Rabn>/Gaa<tm1Rabn>,Stbd1<tm1Bsn>/Stbd1<tm1Bsn>	involves: 129X1/SvJ * C57BL/6	N	27358407
MGI:6780079	M	MP:0010401	increased skeletal muscle glycogen level	Gaa<tm1Rabn>/Gaa<tm1Rabn>,Stbd1<tm1Bsn>/Stbd1<tm1Bsn>	involves: 129X1/SvJ * C57BL/6	N	27358407
MGI:6780172	M	MP:0008545	absent sperm flagellum	Dnah10<em1Yxc>/Dnah10<em1Yxc>	involves: C57BL/6	N	34237282
MGI:6780172	M	MP:0020869	immotile sperm	Dnah10<em1Yxc>/Dnah10<em1Yxc>	involves: C57BL/6	N	34237282
MGI:6780172	M	MP:0001925	male infertility	Dnah10<em1Yxc>/Dnah10<em1Yxc>	involves: C57BL/6	N	34237282
MGI:6780172	M	MP:0009238	coiled sperm flagellum	Dnah10<em1Yxc>/Dnah10<em1Yxc>	involves: C57BL/6	N	34237282
MGI:6780172	M	MP:0009239	short sperm flagellum	Dnah10<em1Yxc>/Dnah10<em1Yxc>	involves: C57BL/6	N	34237282
MGI:6780172	M	MP:0014468	disorganized sperm mitochondrial sheath	Dnah10<em1Yxc>/Dnah10<em1Yxc>	involves: C57BL/6	N	34237282
MGI:6780172	M	MP:0005389	reproductive system phenotype	Dnah10<em1Yxc>/Dnah10<em1Yxc>	involves: C57BL/6	Y	34237282
MGI:6780172	M	MP:0008892	abnormal sperm flagellum morphology	Dnah10<em1Yxc>/Dnah10<em1Yxc>	involves: C57BL/6	N	34237282
MGI:6780172	M	MP:0001156	abnormal spermatogenesis	Dnah10<em1Yxc>/Dnah10<em1Yxc>	involves: C57BL/6	N	34237282
MGI:6780172	M	MP:0002687	oligozoospermia	Dnah10<em1Yxc>/Dnah10<em1Yxc>	involves: C57BL/6	N	34237282
MGI:6780173	M	MP:0002687	oligozoospermia	Dnah10<em2Yxc>/Dnah10<em2Yxc>	involves: C57BL/6	N	34237282
MGI:6780173	M	MP:0001156	abnormal spermatogenesis	Dnah10<em2Yxc>/Dnah10<em2Yxc>	involves: C57BL/6	N	34237282
MGI:6780173	M	MP:0014468	disorganized sperm mitochondrial sheath	Dnah10<em2Yxc>/Dnah10<em2Yxc>	involves: C57BL/6	N	34237282
MGI:6780173	M	MP:0008545	absent sperm flagellum	Dnah10<em2Yxc>/Dnah10<em2Yxc>	involves: C57BL/6	N	34237282
MGI:6780173	M	MP:0009239	short sperm flagellum	Dnah10<em2Yxc>/Dnah10<em2Yxc>	involves: C57BL/6	N	34237282
MGI:6780173	M	MP:0008892	abnormal sperm flagellum morphology	Dnah10<em2Yxc>/Dnah10<em2Yxc>	involves: C57BL/6	N	34237282
MGI:6780173	M	MP:0009238	coiled sperm flagellum	Dnah10<em2Yxc>/Dnah10<em2Yxc>	involves: C57BL/6	N	34237282
MGI:6780173	M	MP:0001925	male infertility	Dnah10<em2Yxc>/Dnah10<em2Yxc>	involves: C57BL/6	N	34237282
MGI:6780173	M	MP:0020869	immotile sperm	Dnah10<em2Yxc>/Dnah10<em2Yxc>	involves: C57BL/6	N	34237282
MGI:6781262	M	MP:0002981	increased liver weight	Plekhn1<tm1.1Hkon>/Plekhn1<tm1.1Hkon>	B6.Cg-Plekhn1<tm1.1Hkon>	N	27616329
MGI:6781262	M	MP:0009288	increased epididymal fat pad weight	Plekhn1<tm1.1Hkon>/Plekhn1<tm1.1Hkon>	B6.Cg-Plekhn1<tm1.1Hkon>	N	27616329
MGI:6781262	M	MP:0001260	increased body weight	Plekhn1<tm1.1Hkon>/Plekhn1<tm1.1Hkon>	B6.Cg-Plekhn1<tm1.1Hkon>	N	27616329
MGI:6781262	M	MP:0005669	increased circulating leptin level	Plekhn1<tm1.1Hkon>/Plekhn1<tm1.1Hkon>	B6.Cg-Plekhn1<tm1.1Hkon>	N	27616329
MGI:6781262	M	MP:0011939	increased food intake	Plekhn1<tm1.1Hkon>/Plekhn1<tm1.1Hkon>	B6.Cg-Plekhn1<tm1.1Hkon>	N	27616329
MGI:6781262	M	MP:0005389	reproductive system phenotype	Plekhn1<tm1.1Hkon>/Plekhn1<tm1.1Hkon>	B6.Cg-Plekhn1<tm1.1Hkon>	Y	27616329
MGI:6781262	M	MP:0011698	abnormal brown adipose tissue physiology	Plekhn1<tm1.1Hkon>/Plekhn1<tm1.1Hkon>	B6.Cg-Plekhn1<tm1.1Hkon>	N	27616329
MGI:6781262	M	MP:0001261	obese	Plekhn1<tm1.1Hkon>/Plekhn1<tm1.1Hkon>	B6.Cg-Plekhn1<tm1.1Hkon>	N	27616329
MGI:6781262	M	MP:0005376	homeostasis/metabolism phenotype	Plekhn1<tm1.1Hkon>/Plekhn1<tm1.1Hkon>	B6.Cg-Plekhn1<tm1.1Hkon>	Y	27616329
MGI:6781262	M	MP:0001433	polyphagia	Plekhn1<tm1.1Hkon>/Plekhn1<tm1.1Hkon>	B6.Cg-Plekhn1<tm1.1Hkon>	N	27616329
MGI:6781930	F	MP:0020418	increased cardiac muscle relaxation	Kcne4<tm1Gwab>/Kcne4<tm1Gwab>	B6.129-Kcne4<tm1Gwab>	N	26399785
MGI:6781930	M	MP:0020345	abnormal myocardial fiber currents	Kcne4<tm1Gwab>/Kcne4<tm1Gwab>	B6.129-Kcne4<tm1Gwab>	N	26399785
MGI:6790238	M	MP:0001402	decreased locomotor activity	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790238	M	MP:0002152	abnormal brain morphology	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790238	M	MP:0020357	abnormal excitatory synapse morphology	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790238	M	MP:0012306	enhanced spatial learning	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790238	M	MP:0004753	abnormal miniature excitatory postsynaptic currents	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790238	M	MP:0005394	taste/olfaction phenotype	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	Y	31285321
MGI:6790238	M	MP:0002920	decreased paired-pulse facilitation	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790238	M	MP:0005386	behavior/neurological phenotype	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	Y	31285321
MGI:6790238	M	MP:0014375	increased miniature excitatory postsynaptic current frequency	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790238	M	MP:0005404	abnormal axon morphology	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790238	M	MP:0014373	increased miniature excitatory postsynaptic current amplitude	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790238	M	MP:0001441	increased grooming behavior	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790238	M	MP:0020351	decreased vocalization	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790238	M	MP:0002557	abnormal social/conspecific interaction behavior	Ank2<em1Bnt>/Ank2<em1Bnt>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790239	M	MP:0012306	enhanced spatial learning	Ank2<em1Bnt>/Ank2<+>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790239	M	MP:0005386	behavior/neurological phenotype	Ank2<em1Bnt>/Ank2<+>	C57BL/6J-Ank2<em1Bnt>	Y	31285321
MGI:6790239	M	MP:0005404	abnormal axon morphology	Ank2<em1Bnt>/Ank2<+>	C57BL/6J-Ank2<em1Bnt>	N	31285321
MGI:6790243	M	MP:0005404	abnormal axon morphology	Ank2<tm4.1Bnt>/Ank2<+>,Tg(Nes-cre)1Kln/0	B6.Cg-Ank2<tm4.1Bnt> Tg(Nes-cre)1Kln	N	31285321
MGI:6790243	M	MP:0012306	enhanced spatial learning	Ank2<tm4.1Bnt>/Ank2<+>,Tg(Nes-cre)1Kln/0	B6.Cg-Ank2<tm4.1Bnt> Tg(Nes-cre)1Kln	N	31285321
MGI:6790243	M	MP:0002557	abnormal social/conspecific interaction behavior	Ank2<tm4.1Bnt>/Ank2<+>,Tg(Nes-cre)1Kln/0	B6.Cg-Ank2<tm4.1Bnt> Tg(Nes-cre)1Kln	N	31285321
MGI:6790243	M	MP:0020351	decreased vocalization	Ank2<tm4.1Bnt>/Ank2<+>,Tg(Nes-cre)1Kln/0	B6.Cg-Ank2<tm4.1Bnt> Tg(Nes-cre)1Kln	N	31285321
MGI:6790245	M	MP:0020351	decreased vocalization	Ank2<tm1Bnt>/Ank2<tm1Bnt>	B6.129-Ank2<tm1Bnt>/Bnt	N	31285321
MGI:6790245	M	MP:0012306	enhanced spatial learning	Ank2<tm1Bnt>/Ank2<tm1Bnt>	B6.129-Ank2<tm1Bnt>/Bnt	N	31285321
MGI:6790245	M	MP:0002557	abnormal social/conspecific interaction behavior	Ank2<tm1Bnt>/Ank2<tm1Bnt>	B6.129-Ank2<tm1Bnt>/Bnt	N	31285321
MGI:6790471	M	MP:0001262	decreased body weight	Zdhhc3<tm1.2Lusc>/Zdhhc3<tm1.2Lusc>	involves: 129P2/OlaHsd * C57BL/6	N	27875292
MGI:6802149	M	MP:0030940	impaired autophagy	Laptm4b<em1Huty>/Laptm4b<em1Huty>	C57BL/6-Laptm4b<em1Huty>	N	32693673
MGI:6802149	M	MP:0003037	increased myocardial infarct size	Laptm4b<em1Huty>/Laptm4b<em1Huty>	C57BL/6-Laptm4b<em1Huty>	N	32693673
MGI:6802149	M	MP:0005058	abnormal lysosome morphology	Laptm4b<em1Huty>/Laptm4b<em1Huty>	C57BL/6-Laptm4b<em1Huty>	N	32693673
MGI:6818637	M	MP:0009747	impaired behavioral response to xenobiotic	Cx3cr1<tm1.1(cre)Jung>/Cx3cr1<+>,Sqor<em1Chji>/Sqor<em1Chji>	B6(Cg)-Sqor<em1Chji> Cx3cr1<tm1.1(cre)Jung>	N	32923620
MGI:6827174	F	MP:0010957	abnormal aerobic respiration	Slc16a13<em1Tac>/Slc16a13<em1Tac>	C57BL/6N-Slc16a13<em1Tac>	N	34211098
MGI:6827282	M	MP:0002216	abnormal seminiferous tubule morphology	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0003674	oxidative stress	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0002687	oligozoospermia	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0011594	decreased catalase activity	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0006036	abnormal mitochondrial physiology	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0001925	male infertility	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0006379	abnormal spermatocyte morphology	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0001147	small testis	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0006035	abnormal mitochondrial morphology	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0002675	asthenozoospermia	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0001156	abnormal spermatogenesis	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0013601	increased testis apoptosis	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0004852	decreased testis weight	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827282	M	MP:0006378	abnormal spermatogonia morphology	Alpl<tm1(cre)Nagy>/Alpl<+>,Xrcc1<tm1Pmc>/Xrcc1<tm1Pmc>	involves: 129S1/Sv * 129X1/SvJ	N	30998386
MGI:6827290	M	MP:0005578	teratozoospermia	Tbc1d21<tm1.1Yhln>/Tbc1d21<tm1.1Yhln>	involves: C57BL/6	N	32976492
MGI:6827290	M	MP:0014465	abnormal sperm mitochondrial morphology	Tbc1d21<tm1.1Yhln>/Tbc1d21<tm1.1Yhln>	involves: C57BL/6	N	32976492
MGI:6827290	M	MP:0031356	abnormal outer dense fiber morphology	Tbc1d21<tm1.1Yhln>/Tbc1d21<tm1.1Yhln>	involves: C57BL/6	N	32976492
MGI:6827290	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Tbc1d21<tm1.1Yhln>/Tbc1d21<tm1.1Yhln>	involves: C57BL/6	N	32976492
MGI:6827290	M	MP:0011633	abnormal mitochondrial shape	Tbc1d21<tm1.1Yhln>/Tbc1d21<tm1.1Yhln>	involves: C57BL/6	N	32976492
MGI:6827290	M	MP:0008892	abnormal sperm flagellum morphology	Tbc1d21<tm1.1Yhln>/Tbc1d21<tm1.1Yhln>	involves: C57BL/6	N	32976492
MGI:6827290	M	MP:0009831	abnormal sperm midpiece morphology	Tbc1d21<tm1.1Yhln>/Tbc1d21<tm1.1Yhln>	involves: C57BL/6	N	32976492
MGI:6827290	M	MP:0011629	decreased mitochondrial number	Tbc1d21<tm1.1Yhln>/Tbc1d21<tm1.1Yhln>	involves: C57BL/6	N	32976492
MGI:6827290	M	MP:0002687	oligozoospermia	Tbc1d21<tm1.1Yhln>/Tbc1d21<tm1.1Yhln>	involves: C57BL/6	N	32976492
MGI:6827290	M	MP:0009838	abnormal sperm axoneme morphology	Tbc1d21<tm1.1Yhln>/Tbc1d21<tm1.1Yhln>	involves: C57BL/6	N	32976492
MGI:6827290	M	MP:0020451	decreased sperm progressive motility	Tbc1d21<tm1.1Yhln>/Tbc1d21<tm1.1Yhln>	involves: C57BL/6	N	32976492
MGI:6827290	M	MP:0004543	abnormal sperm physiology	Tbc1d21<tm1.1Yhln>/Tbc1d21<tm1.1Yhln>	involves: C57BL/6	N	32976492
MGI:6827290	M	MP:0001925	male infertility	Tbc1d21<tm1.1Yhln>/Tbc1d21<tm1.1Yhln>	involves: C57BL/6	N	32976492
MGI:6827350	M	MP:0005578	teratozoospermia	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0009647	decreased fertilization frequency	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0009232	abnormal sperm nucleus morphology	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0002675	asthenozoospermia	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0030590	abnormal sperm fibrous sheath morphology	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0001922	reduced male fertility	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0009239	short sperm flagellum	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0008892	abnormal sperm flagellum morphology	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0009837	abnormal sperm end piece morphology	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0002687	oligozoospermia	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0002662	abnormal cauda epididymis morphology	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0001932	abnormal spermiogenesis	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0001935	decreased litter size	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0006380	abnormal spermatid morphology	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0031351	abnormal sperm flagellum thickness	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827350	M	MP:0009230	abnormal sperm head morphology	Lztfl1<tm1e(KOMP)Wtsi>/Lztfl1<tm1e(KOMP)Wtsi>	involves: C57BL/6N	N	34023333
MGI:6827353	F	MP:0002907	abnormal parturition	Ezh2<tm2Sho>/Ezh2<tm2Sho>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	30954472
MGI:6827353	F	MP:0001935	decreased litter size	Ezh2<tm2Sho>/Ezh2<tm2Sho>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	30954472
MGI:6827353	F	MP:0031336	abnormal uterine epithelium development	Ezh2<tm2Sho>/Ezh2<tm2Sho>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	30954472
MGI:6827353	F	MP:0013401	increased endometrial gland number	Ezh2<tm2Sho>/Ezh2<tm2Sho>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	30954472
MGI:6827353	F	MP:0001923	reduced female fertility	Ezh2<tm2Sho>/Ezh2<tm2Sho>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	30954472
MGI:6827353	F	MP:0008876	decreased uterine NK cell number	Ezh2<tm2Sho>/Ezh2<tm2Sho>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	30954472
MGI:6827353	F	MP:0009092	endometrium hyperplasia	Ezh2<tm2Sho>/Ezh2<tm2Sho>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	30954472
MGI:6827353	F	MP:0004514	dystocia	Ezh2<tm2Sho>/Ezh2<tm2Sho>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	30954472
MGI:6827353	F	MP:0009094	abnormal endometrial gland morphology	Ezh2<tm2Sho>/Ezh2<tm2Sho>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	30954472
MGI:6827353	F	MP:0011873	enlarged uterine horn	Ezh2<tm2Sho>/Ezh2<tm2Sho>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	30954472
MGI:6827353	F	MP:0004896	abnormal endometrium morphology	Ezh2<tm2Sho>/Ezh2<tm2Sho>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	30954472
MGI:6827377	M	MP:0009231	detached acrosome	Actl7a<em1Fzh>/Actl7a<em1Fzh>	C57BL/6-Actl7a<em1Fzh>	N	32923619
MGI:6827377	M	MP:0000242	impaired fertilization	Actl7a<em1Fzh>/Actl7a<em1Fzh>	C57BL/6-Actl7a<em1Fzh>	N	32923619
MGI:6827377	M	MP:0008898	abnormal acrosome morphology	Actl7a<em1Fzh>/Actl7a<em1Fzh>	C57BL/6-Actl7a<em1Fzh>	N	32923619
MGI:6827377	M	MP:0001925	male infertility	Actl7a<em1Fzh>/Actl7a<em1Fzh>	C57BL/6-Actl7a<em1Fzh>	N	32923619
MGI:6827377	F	MP:0005389	reproductive system phenotype	Actl7a<em1Fzh>/Actl7a<em1Fzh>	C57BL/6-Actl7a<em1Fzh>	Y	32923619
MGI:6827383	M	MP:0030976	impaired sperm penetration of zona pellucida	Kif9<em1Osb>/Kif9<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32072696
MGI:6827383	M	MP:0001922	reduced male fertility	Kif9<em1Osb>/Kif9<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32072696
MGI:6827383	M	MP:0002675	asthenozoospermia	Kif9<em1Osb>/Kif9<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32072696
MGI:6827383	M	MP:0020451	decreased sperm progressive motility	Kif9<em1Osb>/Kif9<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32072696
MGI:6827383	M	MP:0005389	reproductive system phenotype	Kif9<em1Osb>/Kif9<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	32072696
MGI:6827383	M	MP:0009647	decreased fertilization frequency	Kif9<em1Osb>/Kif9<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	32072696
MGI:6827384	M	MP:0020451	decreased sperm progressive motility	Kif9<em2Osb>/Kif9<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	32072696
MGI:6827384	M	MP:0002675	asthenozoospermia	Kif9<em2Osb>/Kif9<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	32072696
MGI:6827384	M	MP:0001922	reduced male fertility	Kif9<em2Osb>/Kif9<em2Osb>	involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	N	32072696
MGI:6827421	M	MP:0001925	male infertility	Fanci<em2Szh>/Fanci<em2Szh>	Not Specified	N	34373449
MGI:6827421	M	MP:0002687	oligozoospermia	Fanci<em2Szh>/Fanci<em2Szh>	Not Specified	N	34373449
MGI:6827421	M	MP:0014052	increased male germ cell apoptosis	Fanci<em2Szh>/Fanci<em2Szh>	Not Specified	N	34373449
MGI:6827421	M	MP:0004901	decreased male germ cell number	Fanci<em2Szh>/Fanci<em2Szh>	Not Specified	N	34373449
MGI:6827421	M	MP:0004852	decreased testis weight	Fanci<em2Szh>/Fanci<em2Szh>	Not Specified	N	34373449
MGI:6827421	M	MP:0001147	small testis	Fanci<em2Szh>/Fanci<em2Szh>	Not Specified	N	34373449
MGI:6827421	F	MP:0001926	female infertility	Fanci<em2Szh>/Fanci<em2Szh>	Not Specified	N	34373449
MGI:6827421	M	MP:0001154	seminiferous tubule degeneration	Fanci<em2Szh>/Fanci<em2Szh>	Not Specified	N	34373449
MGI:6827421	M	MP:0008878	abnormal DNA methylation during gametogenesis	Fanci<em2Szh>/Fanci<em2Szh>	Not Specified	N	34373449
MGI:6828595	M	MP:0001926	female infertility	Fanci<tm1.1Itl>/Fanci<tm1.1Itl>	involves: C57BL/6J * CBA	N	31219578
MGI:6828595	M	MP:0005159	azoospermia	Fanci<tm1.1Itl>/Fanci<tm1.1Itl>	involves: C57BL/6J * CBA	N	31219578
MGI:6828595	M	MP:0001925	male infertility	Fanci<tm1.1Itl>/Fanci<tm1.1Itl>	involves: C57BL/6J * CBA	N	31219578
MGI:6828730	F	MP:0009142	decreased prepulse inhibition	Zfp804a<em1Yqd>/Zfp804a<em1Yqd>	involves: C57BL/6 * FVB/N	N	33303946
MGI:6828773	M	MP:0002687	oligozoospermia	Armc3<em1Lukf>/Armc3<em1Lukf>	C57BL/6J-Armc3<em1Lukf>	N	34428398
MGI:6828773	M	MP:0006380	abnormal spermatid morphology	Armc3<em1Lukf>/Armc3<em1Lukf>	C57BL/6J-Armc3<em1Lukf>	N	34428398
MGI:6828773	M	MP:0001925	male infertility	Armc3<em1Lukf>/Armc3<em1Lukf>	C57BL/6J-Armc3<em1Lukf>	N	34428398
MGI:6828773	M	MP:0020869	immotile sperm	Armc3<em1Lukf>/Armc3<em1Lukf>	C57BL/6J-Armc3<em1Lukf>	N	34428398
MGI:6830505	M	MP:0005159	azoospermia	Ewsr1<tm1c(EUCOMM)Wtsi>/Ewsr1<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J	N	34100066
MGI:6830505	M	MP:0008261	arrest of male meiosis	Ewsr1<tm1c(EUCOMM)Wtsi>/Ewsr1<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J	N	34100066
MGI:6830505	M	MP:0001930	abnormal meiosis	Ewsr1<tm1c(EUCOMM)Wtsi>/Ewsr1<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J	N	34100066
MGI:6830505	M	MP:0004852	decreased testis weight	Ewsr1<tm1c(EUCOMM)Wtsi>/Ewsr1<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J	N	34100066
MGI:6830505	M	MP:0001925	male infertility	Ewsr1<tm1c(EUCOMM)Wtsi>/Ewsr1<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J	N	34100066
MGI:6830505	M	MP:0008878	abnormal DNA methylation during gametogenesis	Ewsr1<tm1c(EUCOMM)Wtsi>/Ewsr1<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J	N	34100066
MGI:6830505	M	MP:0001155	arrest of spermatogenesis	Ewsr1<tm1c(EUCOMM)Wtsi>/Ewsr1<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J	N	34100066
MGI:6830505	M	MP:0001147	small testis	Ewsr1<tm1c(EUCOMM)Wtsi>/Ewsr1<tm1d(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J	N	34100066
MGI:6830973	M	MP:0002169	no abnormal phenotype detected	4921539E11Rik<em1Osb>/4921539E11Rik<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34290169
MGI:6830974	M	MP:0005389	reproductive system phenotype	Ctxnd2<em1Osb>/Ctxnd2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34290169
MGI:6830975	M	MP:0005389	reproductive system phenotype	Tmem210<em1Osb>/Tmem210<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34290169
MGI:6830976	M	MP:0005389	reproductive system phenotype	Plscr1l1<em1Kzt>/Plscr1l1<em1Kzt>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34290169
MGI:6830978	M	MP:0005389	reproductive system phenotype	Cby2<em1Osb>/Cby2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34290169
MGI:6830979	M	MP:0005389	reproductive system phenotype	Ldhal6b<em1Osb>/Ldhal6b<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34290169
MGI:6830981	M	MP:0005389	reproductive system phenotype	Rasef<em1Osb>/Rasef<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34290169
MGI:6830982	M	MP:0005389	reproductive system phenotype	Slc25a2<em1Osb>/Slc25a2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34290169
MGI:6830983	M	MP:0005389	reproductive system phenotype	Slc25a41<em1Osb>/Slc25a41<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34290169
MGI:6830985	M	MP:0005389	reproductive system phenotype	Smim8<em1Ncvc>/Smim8<em1Ncvc>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34290169
MGI:6830987	M	MP:0005389	reproductive system phenotype	Smim9<em1Ncvc>/Y	involves: C57BL/6NJcl * DBA/2NJcl	Y	34290169
MGI:6830988	M	MP:0005389	reproductive system phenotype	Tomm20l<em1Kzt>/Tomm20l<em1Kzt>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34290169
MGI:6830991	M	MP:0004852	decreased testis weight	Zcwpw1<em1(IMPC)Tcp>/Zcwpw1<em1(IMPC)Tcp>	C57BL/6N-Zcwpw1<em1(IMPC)Tcp>	N	32744506
MGI:6830991	F	MP:0001926	female infertility	Zcwpw1<em1(IMPC)Tcp>/Zcwpw1<em1(IMPC)Tcp>	C57BL/6N-Zcwpw1<em1(IMPC)Tcp>	N	32744506
MGI:6830991	M	MP:0008261	arrest of male meiosis	Zcwpw1<em1(IMPC)Tcp>/Zcwpw1<em1(IMPC)Tcp>	C57BL/6N-Zcwpw1<em1(IMPC)Tcp>	N	32744506
MGI:6830991	M	MP:0010948	abnormal double-strand DNA break repair	Zcwpw1<em1(IMPC)Tcp>/Zcwpw1<em1(IMPC)Tcp>	C57BL/6N-Zcwpw1<em1(IMPC)Tcp>	N	32744506
MGI:6830991	M	MP:0001147	small testis	Zcwpw1<em1(IMPC)Tcp>/Zcwpw1<em1(IMPC)Tcp>	C57BL/6N-Zcwpw1<em1(IMPC)Tcp>	N	32744506
MGI:6830991	M	MP:0005159	azoospermia	Zcwpw1<em1(IMPC)Tcp>/Zcwpw1<em1(IMPC)Tcp>	C57BL/6N-Zcwpw1<em1(IMPC)Tcp>	N	32744506
MGI:6830991	M	MP:0008967	absent chiasmata formation	Zcwpw1<em1(IMPC)Tcp>/Zcwpw1<em1(IMPC)Tcp>	C57BL/6N-Zcwpw1<em1(IMPC)Tcp>	N	32744506
MGI:6830991	M	MP:0001925	male infertility	Zcwpw1<em1(IMPC)Tcp>/Zcwpw1<em1(IMPC)Tcp>	C57BL/6N-Zcwpw1<em1(IMPC)Tcp>	N	32744506
MGI:6830991	M	MP:0009451	abnormal chromosomal synapsis	Zcwpw1<em1(IMPC)Tcp>/Zcwpw1<em1(IMPC)Tcp>	C57BL/6N-Zcwpw1<em1(IMPC)Tcp>	N	32744506
MGI:6831616	M	MP:0005169	abnormal male meiosis	Ankrd31<em1Flor>/Ankrd31<em1Flor>	C57BL/6JCrl-Ankrd31<em1Flor>	N	34820371
MGI:6831616	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Ankrd31<em1Flor>/Ankrd31<em1Flor>	C57BL/6JCrl-Ankrd31<em1Flor>	N	34820371
MGI:6831616	M	MP:0020451	decreased sperm progressive motility	Ankrd31<em1Flor>/Ankrd31<em1Flor>	C57BL/6JCrl-Ankrd31<em1Flor>	N	34820371
MGI:6831616	M	MP:0004852	decreased testis weight	Ankrd31<em1Flor>/Ankrd31<em1Flor>	C57BL/6JCrl-Ankrd31<em1Flor>	N	34820371
MGI:6831616	M	MP:0009230	abnormal sperm head morphology	Ankrd31<em1Flor>/Ankrd31<em1Flor>	C57BL/6JCrl-Ankrd31<em1Flor>	N	34820371
MGI:6831616	F	MP:0005389	reproductive system phenotype	Ankrd31<em1Flor>/Ankrd31<em1Flor>	C57BL/6JCrl-Ankrd31<em1Flor>	Y	34820371
MGI:6831616	M	MP:0002675	asthenozoospermia	Ankrd31<em1Flor>/Ankrd31<em1Flor>	C57BL/6JCrl-Ankrd31<em1Flor>	N	34820371
MGI:6831616	M	MP:0009232	abnormal sperm nucleus morphology	Ankrd31<em1Flor>/Ankrd31<em1Flor>	C57BL/6JCrl-Ankrd31<em1Flor>	N	34820371
MGI:6831616	M	MP:0002687	oligozoospermia	Ankrd31<em1Flor>/Ankrd31<em1Flor>	C57BL/6JCrl-Ankrd31<em1Flor>	N	34820371
MGI:6831616	M	MP:0001925	male infertility	Ankrd31<em1Flor>/Ankrd31<em1Flor>	C57BL/6JCrl-Ankrd31<em1Flor>	N	34820371
MGI:6831616	M	MP:0001147	small testis	Ankrd31<em1Flor>/Ankrd31<em1Flor>	C57BL/6JCrl-Ankrd31<em1Flor>	N	34820371
MGI:6831618	M	MP:0009230	abnormal sperm head morphology	Ankrd31<em2Flor>/Ankrd31<em2Flor>	C57BL/6JCrl-Ankrd31<em2Flor>	N	34820371
MGI:6831618	M	MP:0009232	abnormal sperm nucleus morphology	Ankrd31<em2Flor>/Ankrd31<em2Flor>	C57BL/6JCrl-Ankrd31<em2Flor>	N	34820371
MGI:6831618	F	MP:0005389	reproductive system phenotype	Ankrd31<em2Flor>/Ankrd31<em2Flor>	C57BL/6JCrl-Ankrd31<em2Flor>	N	34820371
MGI:6831618	M	MP:0001925	male infertility	Ankrd31<em2Flor>/Ankrd31<em2Flor>	C57BL/6JCrl-Ankrd31<em2Flor>	N	34820371
MGI:6831618	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Ankrd31<em2Flor>/Ankrd31<em2Flor>	C57BL/6JCrl-Ankrd31<em2Flor>	N	34820371
MGI:6831618	M	MP:0005169	abnormal male meiosis	Ankrd31<em2Flor>/Ankrd31<em2Flor>	C57BL/6JCrl-Ankrd31<em2Flor>	N	34820371
MGI:6831618	M	MP:0004852	decreased testis weight	Ankrd31<em2Flor>/Ankrd31<em2Flor>	C57BL/6JCrl-Ankrd31<em2Flor>	N	34820371
MGI:6831618	M	MP:0002687	oligozoospermia	Ankrd31<em2Flor>/Ankrd31<em2Flor>	C57BL/6JCrl-Ankrd31<em2Flor>	N	34820371
MGI:6831618	M	MP:0002675	asthenozoospermia	Ankrd31<em2Flor>/Ankrd31<em2Flor>	C57BL/6JCrl-Ankrd31<em2Flor>	N	34820371
MGI:6831618	M	MP:0020451	decreased sperm progressive motility	Ankrd31<em2Flor>/Ankrd31<em2Flor>	C57BL/6JCrl-Ankrd31<em2Flor>	N	34820371
MGI:6831618	M	MP:0001147	small testis	Ankrd31<em2Flor>/Ankrd31<em2Flor>	C57BL/6JCrl-Ankrd31<em2Flor>	N	34820371
MGI:6831620	M	MP:0005169	abnormal male meiosis	Ankrd31<em3Flor>/Ankrd31<em3Flor>	C57BL/6JCrl-Ankrd31<em3Flor>	N	34820371
MGI:6831620	M	MP:0001925	male infertility	Ankrd31<em3Flor>/Ankrd31<em3Flor>	C57BL/6JCrl-Ankrd31<em3Flor>	N	34820371
MGI:6831620	M	MP:0002675	asthenozoospermia	Ankrd31<em3Flor>/Ankrd31<em3Flor>	C57BL/6JCrl-Ankrd31<em3Flor>	N	34820371
MGI:6831620	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Ankrd31<em3Flor>/Ankrd31<em3Flor>	C57BL/6JCrl-Ankrd31<em3Flor>	N	34820371
MGI:6831620	M	MP:0001147	small testis	Ankrd31<em3Flor>/Ankrd31<em3Flor>	C57BL/6JCrl-Ankrd31<em3Flor>	N	34820371
MGI:6831620	F	MP:0005389	reproductive system phenotype	Ankrd31<em3Flor>/Ankrd31<em3Flor>	C57BL/6JCrl-Ankrd31<em3Flor>	N	34820371
MGI:6831620	M	MP:0002687	oligozoospermia	Ankrd31<em3Flor>/Ankrd31<em3Flor>	C57BL/6JCrl-Ankrd31<em3Flor>	N	34820371
MGI:6831620	M	MP:0009230	abnormal sperm head morphology	Ankrd31<em3Flor>/Ankrd31<em3Flor>	C57BL/6JCrl-Ankrd31<em3Flor>	N	34820371
MGI:6831620	M	MP:0020451	decreased sperm progressive motility	Ankrd31<em3Flor>/Ankrd31<em3Flor>	C57BL/6JCrl-Ankrd31<em3Flor>	N	34820371
MGI:6831620	M	MP:0009232	abnormal sperm nucleus morphology	Ankrd31<em3Flor>/Ankrd31<em3Flor>	C57BL/6JCrl-Ankrd31<em3Flor>	N	34820371
MGI:6831620	M	MP:0004852	decreased testis weight	Ankrd31<em3Flor>/Ankrd31<em3Flor>	C57BL/6JCrl-Ankrd31<em3Flor>	N	34820371
MGI:6835643	F	MP:0005389	reproductive system phenotype	Hdac8<tm1.1Eno>/Hdac8<tm1.1Eno>,Tg(Zp3-cre)93Knw/0	involves: 129S6/SvEvTac * C57BL/6J	Y	30620721
MGI:6835645	F	MP:0001923	reduced female fertility	Hdac8<tm1.1Eno>/Hdac8<tm1.2Eno>,Tg(Ddx4-cre)1Dcas/0	involves: 129S6/SvEvTac * C57BL/6J * FVB	N	30620721
MGI:6835645	F	MP:0001125	abnormal oocyte morphology	Hdac8<tm1.1Eno>/Hdac8<tm1.2Eno>,Tg(Ddx4-cre)1Dcas/0	involves: 129S6/SvEvTac * C57BL/6J * FVB	N	30620721
MGI:6835645	F	MP:0005168	abnormal female meiosis	Hdac8<tm1.1Eno>/Hdac8<tm1.2Eno>,Tg(Ddx4-cre)1Dcas/0	involves: 129S6/SvEvTac * C57BL/6J * FVB	N	30620721
MGI:6835645	F	MP:0001931	abnormal oogenesis	Hdac8<tm1.1Eno>/Hdac8<tm1.2Eno>,Tg(Ddx4-cre)1Dcas/0	involves: 129S6/SvEvTac * C57BL/6J * FVB	N	30620721
MGI:6835645	F	MP:0001935	decreased litter size	Hdac8<tm1.1Eno>/Hdac8<tm1.2Eno>,Tg(Ddx4-cre)1Dcas/0	involves: 129S6/SvEvTac * C57BL/6J * FVB	N	30620721
MGI:6835645	F	MP:0005389	reproductive system phenotype	Hdac8<tm1.1Eno>/Hdac8<tm1.2Eno>,Tg(Ddx4-cre)1Dcas/0	involves: 129S6/SvEvTac * C57BL/6J * FVB	Y	30620721
MGI:6835805	M	MP:0006379	abnormal spermatocyte morphology	Rnf138<tm1.1Lwan>/Rnf138<tm1.1Lwan>	Not Specified	N	28518149
MGI:6835805	M	MP:0001153	small seminiferous tubules	Rnf138<tm1.1Lwan>/Rnf138<tm1.1Lwan>	Not Specified	N	28518149
MGI:6835805	M	MP:0013601	increased testis apoptosis	Rnf138<tm1.1Lwan>/Rnf138<tm1.1Lwan>	Not Specified	N	28518149
MGI:6835805	M	MP:0006378	abnormal spermatogonia morphology	Rnf138<tm1.1Lwan>/Rnf138<tm1.1Lwan>	Not Specified	N	28518149
MGI:6835805	M	MP:0004852	decreased testis weight	Rnf138<tm1.1Lwan>/Rnf138<tm1.1Lwan>	Not Specified	N	28518149
MGI:6835805	M	MP:0003205	testicular atrophy	Rnf138<tm1.1Lwan>/Rnf138<tm1.1Lwan>	Not Specified	N	28518149
MGI:6835805	M	MP:0001156	abnormal spermatogenesis	Rnf138<tm1.1Lwan>/Rnf138<tm1.1Lwan>	Not Specified	N	28518149
MGI:6835805	M	MP:0001147	small testis	Rnf138<tm1.1Lwan>/Rnf138<tm1.1Lwan>	Not Specified	N	28518149
MGI:6835805	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Rnf138<tm1.1Lwan>/Rnf138<tm1.1Lwan>	Not Specified	N	28518149
MGI:6835805	M	MP:0001922	reduced male fertility	Rnf138<tm1.1Lwan>/Rnf138<tm1.1Lwan>	Not Specified	N	28518149
MGI:6835805	M	MP:0002687	oligozoospermia	Rnf138<tm1.1Lwan>/Rnf138<tm1.1Lwan>	Not Specified	N	28518149
MGI:6836745	F	MP:0002681	increased corpora lutea number	Tgfbr3l<em2Djb>/Tgfbr3l<em2Djb>	C57BL/6N-Tgfbr3l<em2Djb>	N	34910520
MGI:6836745	F	MP:0020152	abnormal oocyte number	Tgfbr3l<em2Djb>/Tgfbr3l<em2Djb>	C57BL/6N-Tgfbr3l<em2Djb>	N	34910520
MGI:6836745	F	MP:0011128	increased tertiary ovarian follicle number	Tgfbr3l<em2Djb>/Tgfbr3l<em2Djb>	C57BL/6N-Tgfbr3l<em2Djb>	N	34910520
MGI:6836745	F	MP:0001934	increased litter size	Tgfbr3l<em2Djb>/Tgfbr3l<em2Djb>	C57BL/6N-Tgfbr3l<em2Djb>	N	34910520
MGI:6836745	F	MP:0005389	reproductive system phenotype	Tgfbr3l<em2Djb>/Tgfbr3l<em2Djb>	C57BL/6N-Tgfbr3l<em2Djb>	Y	34910520
MGI:6836745	F	MP:0001750	increased circulating follicle stimulating hormone level	Tgfbr3l<em2Djb>/Tgfbr3l<em2Djb>	C57BL/6N-Tgfbr3l<em2Djb>	N	34910520
MGI:6836747	F	MP:0004855	increased ovary weight	Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>,Tgfbr3<tm1.1Hlin>/Tgfbr3<tm1.1Hlin>,Tgfbr3l<em2Djb>/Tgfbr3l<em2Djb>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6N	N	34910520
MGI:6836747	F	MP:0005131	increased follicle stimulating hormone level	Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>,Tgfbr3<tm1.1Hlin>/Tgfbr3<tm1.1Hlin>,Tgfbr3l<em2Djb>/Tgfbr3l<em2Djb>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6N	N	34910520
MGI:6836747	F	MP:0001750	increased circulating follicle stimulating hormone level	Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>,Tgfbr3<tm1.1Hlin>/Tgfbr3<tm1.1Hlin>,Tgfbr3l<em2Djb>/Tgfbr3l<em2Djb>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6N	N	34910520
MGI:6838379	M	MP:0009230	abnormal sperm head morphology	Zdhhc19<em1Cya>/Zdhhc19<em1Cya>	C57BL/6N-Zdhhc19<em1Cya>/Cya	N	34445597
MGI:6838379	M	MP:0002675	asthenozoospermia	Zdhhc19<em1Cya>/Zdhhc19<em1Cya>	C57BL/6N-Zdhhc19<em1Cya>/Cya	N	34445597
MGI:6838379	M	MP:0001925	male infertility	Zdhhc19<em1Cya>/Zdhhc19<em1Cya>	C57BL/6N-Zdhhc19<em1Cya>/Cya	N	34445597
MGI:6838379	M	MP:0004542	impaired acrosome reaction	Zdhhc19<em1Cya>/Zdhhc19<em1Cya>	C57BL/6N-Zdhhc19<em1Cya>/Cya	N	34445597
MGI:6838379	M	MP:0009238	coiled sperm flagellum	Zdhhc19<em1Cya>/Zdhhc19<em1Cya>	C57BL/6N-Zdhhc19<em1Cya>/Cya	N	34445597
MGI:6838379	M	MP:0009647	decreased fertilization frequency	Zdhhc19<em1Cya>/Zdhhc19<em1Cya>	C57BL/6N-Zdhhc19<em1Cya>/Cya	N	34445597
MGI:6838379	M	MP:0009237	kinked sperm flagellum	Zdhhc19<em1Cya>/Zdhhc19<em1Cya>	C57BL/6N-Zdhhc19<em1Cya>/Cya	N	34445597
MGI:6838388	F	MP:0001923	reduced female fertility	Cenpv<tm1d(EUCOMM)Hmgu>/Cenpv<tm1d(EUCOMM)Hmgu>	involves: C57BL/6N	N	34764261
MGI:6838388	F	MP:0009761	abnormal meiotic spindle morphology	Cenpv<tm1d(EUCOMM)Hmgu>/Cenpv<tm1d(EUCOMM)Hmgu>	involves: C57BL/6N	N	34764261
MGI:6838388	M	MP:0005389	reproductive system phenotype	Cenpv<tm1d(EUCOMM)Hmgu>/Cenpv<tm1d(EUCOMM)Hmgu>	involves: C57BL/6N	Y	34764261
MGI:6838388	F	MP:0005168	abnormal female meiosis	Cenpv<tm1d(EUCOMM)Hmgu>/Cenpv<tm1d(EUCOMM)Hmgu>	involves: C57BL/6N	N	34764261
MGI:6838388	F	MP:0014443	impaired polar body extrusion	Cenpv<tm1d(EUCOMM)Hmgu>/Cenpv<tm1d(EUCOMM)Hmgu>	involves: C57BL/6N	N	34764261
MGI:6838389	F	MP:0014443	impaired polar body extrusion	Cenpv<tm1c(EUCOMM)Hmgu>/Cenpv<tm1c(EUCOMM)Hmgu>,Tg(Spo11-cre)1Rsw/0	involves: C57BL/6N	N	34764261
MGI:6838391	F	MP:0014443	impaired polar body extrusion	Cenpv<tm1c(EUCOMM)Hmgu>/Cenpv<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	34764261
MGI:6838392	F	MP:0005168	abnormal female meiosis	Cenpv<tm1c(EUCOMM)Hmgu>/Cenpv<tm1c(EUCOMM)Hmgu>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6N * FVB	N	34764261
MGI:6842361	F	MP:0005389	reproductive system phenotype	C2cd6<tm1Jw>/C2cd6<tm1Jw>	involves: 129S4/SvJae * C57BL/6	Y	34919125
MGI:6842361	M	MP:0000242	impaired fertilization	C2cd6<tm1Jw>/C2cd6<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	34919125
MGI:6842361	M	MP:0009282	decreased hyperactivated sperm motility	C2cd6<tm1Jw>/C2cd6<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	34919125
MGI:6842361	M	MP:0008892	abnormal sperm flagellum morphology	C2cd6<tm1Jw>/C2cd6<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	34919125
MGI:6842361	M	MP:0001925	male infertility	C2cd6<tm1Jw>/C2cd6<tm1Jw>	involves: 129S4/SvJae * C57BL/6	N	34919125
MGI:6842953	M	MP:0014052	increased male germ cell apoptosis	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0004852	decreased testis weight	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0002687	oligozoospermia	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0001147	small testis	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0009282	decreased hyperactivated sperm motility	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0002784	abnormal Sertoli cell morphology	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0013601	increased testis apoptosis	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0003205	testicular atrophy	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0008892	abnormal sperm flagellum morphology	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0001146	abnormal testis morphology	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0006380	abnormal spermatid morphology	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0002216	abnormal seminiferous tubule morphology	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0002674	abnormal sperm motility	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0005578	teratozoospermia	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0001925	male infertility	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0009238	coiled sperm flagellum	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	F	MP:0005389	reproductive system phenotype	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	Y	33526452
MGI:6842953	M	MP:0009230	abnormal sperm head morphology	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842953	M	MP:0009831	abnormal sperm midpiece morphology	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0	involves: 129S2/SvPas * C57BL/6	N	33526452
MGI:6842960	M	MP:0005389	reproductive system phenotype	Ggcx<tm1Sinos>/Ggcx<tm1Sinos>,Tg(AMH-cre)#Sinos/0,Tg(AMH-Gja1*)#Sinos/0	involves: 129S2/SvPas * C57BL/6	Y	33526452
MGI:6845052	M	MP:0005159	azoospermia	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845052	M	MP:0001925	male infertility	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845052	M	MP:0003205	testicular atrophy	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845052	M	MP:0001155	arrest of spermatogenesis	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845052	M	MP:0001153	small seminiferous tubules	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845052	M	MP:0006380	abnormal spermatid morphology	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845052	M	MP:0014052	increased male germ cell apoptosis	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845052	M	MP:0002216	abnormal seminiferous tubule morphology	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845052	M	MP:0001147	small testis	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845052	M	MP:0008469	abnormal protein level	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845052	M	MP:0004852	decreased testis weight	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845052	M	MP:0004901	decreased male germ cell number	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845052	M	MP:0006379	abnormal spermatocyte morphology	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845052	M	MP:0013601	increased testis apoptosis	Csnk2b<tm1.1Bb>/Csnk2b<tm1.2Bb>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ	N	31755150
MGI:6845061	F	MP:0003718	maternal effect	Dppa2<tm1.1Reik>/Dppa2<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: C57BL/6 * FVB/N	N	34931676
MGI:6845063	F	MP:0003718	maternal effect	Dppa2<tm2.1Reik>/Dppa2<tm2.1Reik>,Dppa4<tm2.1Reik>/Dppa4<tm2.1Reik>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: C57BL/6 * FVB/N	N	34931676
MGI:6845064	F	MP:0003718	maternal effect	Dppa4<tm1.1Reik>/Dppa4<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: C57BL/6 * FVB/N	N	34931676
MGI:6845066	F	MP:0003718	maternal effect	Dppa4<tm1.2Reik>/Dppa4<+>	involves: C57BL/6 * FVB/N	N	34931676
MGI:6845069	F	MP:0003718	maternal effect	Del(16Dppa4-Dppa2)1Reik/+	involves: C57BL/6 * FVB/N	N	34931676
MGI:6845069	M	MP:0005389	reproductive system phenotype	Del(16Dppa4-Dppa2)1Reik/+	involves: C57BL/6 * FVB/N	Y	34931676
MGI:6845081	F	MP:0013508	increased granulosa cell apoptosis	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0031239	increased atretic ovarian follicle number	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0011129	decreased tertiary ovarian follicle number	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0011130	absent tertiary ovarian follicles	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0004856	decreased ovary weight	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0005431	decreased oocyte number	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0010948	abnormal double-strand DNA break repair	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0031381	decreased secondary ovarian follicle number	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0004833	ovary atrophy	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0011121	decreased primordial ovarian follicle number	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0011122	absent primordial ovarian follicles	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0001926	female infertility	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0031382	absent secondary ovarian follicles	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0031020	premature ovarian failure	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6845081	F	MP:0011126	absent primary ovarian follicles	Csnk2b<tm1.1Bb>/Csnk2b<tm1.1Bb>,Tg(Gdf9-icre)5092Coo/0	involves: 129S2/SvPasCrl * C57BL/6	N	29725001
MGI:6849947	M	MP:0002674	abnormal sperm motility	Spmip10<em1Osb>/Spmip10<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34446558
MGI:6849947	M	MP:0005389	reproductive system phenotype	Spmip10<em1Osb>/Spmip10<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34446558
MGI:6849948	M	MP:0005389	reproductive system phenotype	Spata33<em1Osb>/Spata33<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34446558
MGI:6849948	M	MP:0001922	reduced male fertility	Spata33<em1Osb>/Spata33<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34446558
MGI:6849948	M	MP:0002674	abnormal sperm motility	Spata33<em1Osb>/Spata33<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34446558
MGI:6849948	M	MP:0000242	impaired fertilization	Spata33<em1Osb>/Spata33<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34446558
MGI:6849948	M	MP:0009831	abnormal sperm midpiece morphology	Spata33<em1Osb>/Spata33<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34446558
MGI:6849950	M	MP:0002674	abnormal sperm motility	Spata33<em2Osb>/Spata33<em2Osb>	C57BL/6N-Spata33<em2Osb>/Osb	N	34446558
MGI:6849975	F	MP:0009011	prolonged diestrus	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	F	MP:0002682	decreased mature ovarian follicle number	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	F	MP:0001143	constricted vagina orifice	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	F	MP:0004895	vagina atrophy	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	M	MP:0001402	decreased locomotor activity	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	F	MP:0009708	vaginal septum	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	F	MP:0001926	female infertility	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	F	MP:0001927	abnormal estrous cycle	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	F	MP:0009014	prolonged proestrus	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	M	MP:0005389	reproductive system phenotype	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	Y	17121547
MGI:6849975	F	MP:0001129	impaired ovarian folliculogenesis	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	F	MP:0001142	abnormal vagina orifice morphology	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	F	MP:0001140	abnormal vagina epithelium morphology	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	F	MP:0009018	short estrus	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	F	MP:0001127	small ovary	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6849975	F	MP:0031420	decreased superovulation rate	Mdk<tm1Tmu>/Mdk<tm1Tmu>,Ptn<tm1Tmu>/Ptn<tm1Tmu>	B6.129S2-Mdk<tm1Tmu> Ptn<tm1Tmu>	N	17121547
MGI:6850117	F	MP:0001927	abnormal estrous cycle	Ptprn<tm1Aln>/Ptprn<tm1Aln>,Ptprn2<tm1Aln>/Ptprn2<tm1Aln>	involves: 129S4/SvJae * C57BL/6N	N	16269463
MGI:6850117	F	MP:0005132	decreased luteinizing hormone level	Ptprn<tm1Aln>/Ptprn<tm1Aln>,Ptprn2<tm1Aln>/Ptprn2<tm1Aln>	involves: 129S4/SvJae * C57BL/6N	N	16269463
MGI:6850117	F	MP:0001134	absent corpus luteum	Ptprn<tm1Aln>/Ptprn<tm1Aln>,Ptprn2<tm1Aln>/Ptprn2<tm1Aln>	involves: 129S4/SvJae * C57BL/6N	N	16269463
MGI:6850117	F	MP:0005130	decreased follicle stimulating hormone level	Ptprn<tm1Aln>/Ptprn<tm1Aln>,Ptprn2<tm1Aln>/Ptprn2<tm1Aln>	involves: 129S4/SvJae * C57BL/6N	N	16269463
MGI:6850117	F	MP:0001935	decreased litter size	Ptprn<tm1Aln>/Ptprn<tm1Aln>,Ptprn2<tm1Aln>/Ptprn2<tm1Aln>	involves: 129S4/SvJae * C57BL/6N	N	16269463
MGI:6850117	F	MP:0002773	decreased circulating luteinizing hormone level	Ptprn<tm1Aln>/Ptprn<tm1Aln>,Ptprn2<tm1Aln>/Ptprn2<tm1Aln>	involves: 129S4/SvJae * C57BL/6N	N	16269463
MGI:6850117	F	MP:0001926	female infertility	Ptprn<tm1Aln>/Ptprn<tm1Aln>,Ptprn2<tm1Aln>/Ptprn2<tm1Aln>	involves: 129S4/SvJae * C57BL/6N	N	16269463
MGI:6850117	F	MP:0001928	abnormal ovulation	Ptprn<tm1Aln>/Ptprn<tm1Aln>,Ptprn2<tm1Aln>/Ptprn2<tm1Aln>	involves: 129S4/SvJae * C57BL/6N	N	16269463
MGI:6850117	M	MP:0005389	reproductive system phenotype	Ptprn<tm1Aln>/Ptprn<tm1Aln>,Ptprn2<tm1Aln>/Ptprn2<tm1Aln>	involves: 129S4/SvJae * C57BL/6N	Y	16269463
MGI:6850117	F	MP:0001126	abnormal ovary morphology	Ptprn<tm1Aln>/Ptprn<tm1Aln>,Ptprn2<tm1Aln>/Ptprn2<tm1Aln>	involves: 129S4/SvJae * C57BL/6N	N	16269463
MGI:6850117	M	MP:0005376	homeostasis/metabolism phenotype	Ptprn<tm1Aln>/Ptprn<tm1Aln>,Ptprn2<tm1Aln>/Ptprn2<tm1Aln>	involves: 129S4/SvJae * C57BL/6N	Y	16269463
MGI:6850120	M	MP:0002842	increased systemic arterial blood pressure	Clcn2<em1Uis>/Clcn2<+>	C57BL/6N-Clcn2<em1Uis>	N	31727896
MGI:6850120	F	MP:0011460	decreased urine chloride ion level	Clcn2<em1Uis>/Clcn2<+>	C57BL/6N-Clcn2<em1Uis>	N	31727896
MGI:6850619	F	MP:0003674	oxidative stress	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0011125	decreased primary ovarian follicle number	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0001926	female infertility	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0011121	decreased primordial ovarian follicle number	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0002682	decreased mature ovarian follicle number	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0031239	increased atretic ovarian follicle number	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0013508	increased granulosa cell apoptosis	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0009020	prolonged metestrus	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0009018	short estrus	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0012659	decreased superoxide dismutase level	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0011629	decreased mitochondrial number	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0009015	short proestrus	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0031018	decreased granulosa cell proliferation	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0009011	prolonged diestrus	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0004856	decreased ovary weight	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0005431	decreased oocyte number	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0031381	decreased secondary ovarian follicle number	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0006035	abnormal mitochondrial morphology	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0011635	abnormal mitochondrial crista morphology	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0001127	small ovary	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0002636	delayed vaginal opening	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0001927	abnormal estrous cycle	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0003406	failure of zygotic cell division	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0003507	abnormal ovary physiology	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0031420	decreased superovulation rate	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0003582	abnormal ovary development	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850619	F	MP:0005319	abnormal enzyme/coenzyme level	Bmi1<tm1Brn>/Bmi1<tm1Brn>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	N	30906217
MGI:6850681	F	MP:0003845	abnormal decidualization	Atg16l1<tm1c(EUCOMM)Wtsi>/Atg16l1<tm1c(EUCOMM)Wtsi>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	31875883
MGI:6850681	F	MP:0001923	reduced female fertility	Atg16l1<tm1c(EUCOMM)Wtsi>/Atg16l1<tm1c(EUCOMM)Wtsi>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	31875883
MGI:6850681	F	MP:0001935	decreased litter size	Atg16l1<tm1c(EUCOMM)Wtsi>/Atg16l1<tm1c(EUCOMM)Wtsi>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	31875883
MGI:6850681	F	MP:0001729	impaired embryo implantation	Atg16l1<tm1c(EUCOMM)Wtsi>/Atg16l1<tm1c(EUCOMM)Wtsi>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	N	31875883
MGI:6852521	F	MP:0005389	reproductive system phenotype	Kat8<tm1Thl>/Kat8<tm1Thl>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	Y	28506985
MGI:6852522	F	MP:0001926	female infertility	Kat8<tm1Thl>/Kat8<tm1Thl>,Tg(Gdf9-icre)5092Coo/0	involves: 129S1/Sv * C57BL/6	N	28506985
MGI:6852522	F	MP:0003674	oxidative stress	Kat8<tm1Thl>/Kat8<tm1Thl>,Tg(Gdf9-icre)5092Coo/0	involves: 129S1/Sv * C57BL/6	N	28506985
MGI:6852522	F	MP:0004856	decreased ovary weight	Kat8<tm1Thl>/Kat8<tm1Thl>,Tg(Gdf9-icre)5092Coo/0	involves: 129S1/Sv * C57BL/6	N	28506985
MGI:6852522	F	MP:0031239	increased atretic ovarian follicle number	Kat8<tm1Thl>/Kat8<tm1Thl>,Tg(Gdf9-icre)5092Coo/0	involves: 129S1/Sv * C57BL/6	N	28506985
MGI:6852522	F	MP:0001931	abnormal oogenesis	Kat8<tm1Thl>/Kat8<tm1Thl>,Tg(Gdf9-icre)5092Coo/0	involves: 129S1/Sv * C57BL/6	N	28506985
MGI:6852522	F	MP:0001125	abnormal oocyte morphology	Kat8<tm1Thl>/Kat8<tm1Thl>,Tg(Gdf9-icre)5092Coo/0	involves: 129S1/Sv * C57BL/6	N	28506985
MGI:6852522	F	MP:0001127	small ovary	Kat8<tm1Thl>/Kat8<tm1Thl>,Tg(Gdf9-icre)5092Coo/0	involves: 129S1/Sv * C57BL/6	N	28506985
MGI:6852522	F	MP:0012167	abnormal epigenetic regulation of gene expression	Kat8<tm1Thl>/Kat8<tm1Thl>,Tg(Gdf9-icre)5092Coo/0	involves: 129S1/Sv * C57BL/6	N	28506985
MGI:6852522	F	MP:0005431	decreased oocyte number	Kat8<tm1Thl>/Kat8<tm1Thl>,Tg(Gdf9-icre)5092Coo/0	involves: 129S1/Sv * C57BL/6	N	28506985
MGI:6852522	F	MP:0020364	abnormal female germ cell physiology	Kat8<tm1Thl>/Kat8<tm1Thl>,Tg(Gdf9-icre)5092Coo/0	involves: 129S1/Sv * C57BL/6	N	28506985
MGI:6852522	F	MP:0001129	impaired ovarian folliculogenesis	Kat8<tm1Thl>/Kat8<tm1Thl>,Tg(Gdf9-icre)5092Coo/0	involves: 129S1/Sv * C57BL/6	N	28506985
MGI:6852522	F	MP:0031474	increased female germ cell apoptosis	Kat8<tm1Thl>/Kat8<tm1Thl>,Tg(Gdf9-icre)5092Coo/0	involves: 129S1/Sv * C57BL/6	N	28506985
MGI:6852580	M	MP:0001925	male infertility	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Hspa2-cre)1Eddy/0	involves: C57BL/6 * C57BL/6J	N	23258628
MGI:6852580	M	MP:0009230	abnormal sperm head morphology	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Hspa2-cre)1Eddy/0	involves: C57BL/6 * C57BL/6J	N	23258628
MGI:6852580	M	MP:0002686	globozoospermia	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Hspa2-cre)1Eddy/0	involves: C57BL/6 * C57BL/6J	N	23258628
MGI:6852580	M	MP:0008279	arrest of spermiogenesis	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Hspa2-cre)1Eddy/0	involves: C57BL/6 * C57BL/6J	N	23258628
MGI:6852580	M	MP:0009232	abnormal sperm nucleus morphology	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Hspa2-cre)1Eddy/0	involves: C57BL/6 * C57BL/6J	N	23258628
MGI:6852580	M	MP:0008545	absent sperm flagellum	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Hspa2-cre)1Eddy/0	involves: C57BL/6 * C57BL/6J	N	23258628
MGI:6852580	M	MP:0002687	oligozoospermia	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Hspa2-cre)1Eddy/0	involves: C57BL/6 * C57BL/6J	N	23258628
MGI:6852580	M	MP:0020869	immotile sperm	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Hspa2-cre)1Eddy/0	involves: C57BL/6 * C57BL/6J	N	23258628
MGI:6852580	M	MP:0009838	abnormal sperm axoneme morphology	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Hspa2-cre)1Eddy/0	involves: C57BL/6 * C57BL/6J	N	23258628
MGI:6852580	M	MP:0006380	abnormal spermatid morphology	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Hspa2-cre)1Eddy/0	involves: C57BL/6 * C57BL/6J	N	23258628
MGI:6852580	M	MP:0005389	reproductive system phenotype	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Hspa2-cre)1Eddy/0	involves: C57BL/6 * C57BL/6J	Y	23258628
MGI:6852580	M	MP:0031374	abnormal manchette assembly	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Hspa2-cre)1Eddy/0	involves: C57BL/6 * C57BL/6J	N	23258628
MGI:6852580	M	MP:0002631	abnormal epididymis morphology	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Hspa2-cre)1Eddy/0	involves: C57BL/6 * C57BL/6J	N	23258628
MGI:6852583	M	MP:0005389	reproductive system phenotype	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Prm-cre)58Og/0	involves: 129S1/SvImJ * 129S4/SvJae	Y	23258628
MGI:6852584	M	MP:0005389	reproductive system phenotype	Meig1<tm1.1Zzha>/Meig1<tm1.1Zzha>,Tg(Amh-cre)8815Reb/0	involves: 129S1/SvImJ * FVB/N	Y	23258628
MGI:6852756	M	MP:0004749	nonsyndromic hearing loss	Smpx<em1Jgao>/Y	CBA/CaJ-Smpx<em1Jgao>	N	34722533
MGI:6852756	M	MP:0004597	increased susceptibility to noise-induced hearing loss	Smpx<em1Jgao>/Y	CBA/CaJ-Smpx<em1Jgao>	N	34722533
MGI:6852756	M	MP:0004404	cochlear outer hair cell degeneration	Smpx<em1Jgao>/Y	CBA/CaJ-Smpx<em1Jgao>	N	34722533
MGI:6852756	M	MP:0011967	increased or absent threshold for auditory brainstem response	Smpx<em1Jgao>/Y	CBA/CaJ-Smpx<em1Jgao>	N	34722533
MGI:6852756	M	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology	Smpx<em1Jgao>/Y	CBA/CaJ-Smpx<em1Jgao>	N	34722533
MGI:6852756	M	MP:0004736	abnormal distortion product otoacoustic emission	Smpx<em1Jgao>/Y	CBA/CaJ-Smpx<em1Jgao>	N	34722533
MGI:6852756	M	MP:0004399	abnormal cochlear outer hair cell morphology	Smpx<em1Jgao>/Y	CBA/CaJ-Smpx<em1Jgao>	N	34722533
MGI:6852757	M	MP:0004399	abnormal cochlear outer hair cell morphology	Smpx<em2Jgao>/Y	CBA/CaJ-Smpx<em2Jgao>	N	34722533
MGI:6852757	M	MP:0004749	nonsyndromic hearing loss	Smpx<em2Jgao>/Y	CBA/CaJ-Smpx<em2Jgao>	N	34722533
MGI:6852757	M	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology	Smpx<em2Jgao>/Y	CBA/CaJ-Smpx<em2Jgao>	N	34722533
MGI:6852757	M	MP:0004736	abnormal distortion product otoacoustic emission	Smpx<em2Jgao>/Y	CBA/CaJ-Smpx<em2Jgao>	N	34722533
MGI:6852757	M	MP:0004404	cochlear outer hair cell degeneration	Smpx<em2Jgao>/Y	CBA/CaJ-Smpx<em2Jgao>	N	34722533
MGI:6852757	M	MP:0004597	increased susceptibility to noise-induced hearing loss	Smpx<em2Jgao>/Y	CBA/CaJ-Smpx<em2Jgao>	N	34722533
MGI:6852757	M	MP:0011967	increased or absent threshold for auditory brainstem response	Smpx<em2Jgao>/Y	CBA/CaJ-Smpx<em2Jgao>	N	34722533
MGI:6852759	F	MP:0011967	increased or absent threshold for auditory brainstem response	Smpx<em1Jgao>/Smpx<em1Jgao>	CBA/CaJ-Smpx<em1Jgao>	N	34722533
MGI:6852759	F	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology	Smpx<em1Jgao>/Smpx<em1Jgao>	CBA/CaJ-Smpx<em1Jgao>	N	34722533
MGI:6852759	F	MP:0004749	nonsyndromic hearing loss	Smpx<em1Jgao>/Smpx<em1Jgao>	CBA/CaJ-Smpx<em1Jgao>	N	34722533
MGI:6852760	F	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology	Smpx<em2Jgao>/Smpx<em2Jgao>	CBA/CaJ-Smpx<em2Jgao>	N	34722533
MGI:6852760	F	MP:0004749	nonsyndromic hearing loss	Smpx<em2Jgao>/Smpx<em2Jgao>	CBA/CaJ-Smpx<em2Jgao>	N	34722533
MGI:6852760	F	MP:0011967	increased or absent threshold for auditory brainstem response	Smpx<em2Jgao>/Smpx<em2Jgao>	CBA/CaJ-Smpx<em2Jgao>	N	34722533
MGI:6852761	F	MP:0011967	increased or absent threshold for auditory brainstem response	Smpx<em1Jgao>/Smpx<+>	CBA/CaJ-Smpx<em1Jgao>	N	34722533
MGI:6852761	F	MP:0004749	nonsyndromic hearing loss	Smpx<em1Jgao>/Smpx<+>	CBA/CaJ-Smpx<em1Jgao>	N	34722533
MGI:6852762	F	MP:0011967	increased or absent threshold for auditory brainstem response	Smpx<em2Jgao>/Smpx<+>	CBA/CaJ-Smpx<em2Jgao>	N	34722533
MGI:6852762	F	MP:0004749	nonsyndromic hearing loss	Smpx<em2Jgao>/Smpx<+>	CBA/CaJ-Smpx<em2Jgao>	N	34722533
MGI:6852794	F	MP:0001935	decreased litter size	Adam10<tm2Psa>/Adam10<tm2Psa>,Tg(Tek-cre)1Ywa/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	32385775
MGI:6852794	F	MP:0001614	abnormal blood vessel morphology	Adam10<tm2Psa>/Adam10<tm2Psa>,Tg(Tek-cre)1Ywa/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	32385775
MGI:6852794	F	MP:0006056	increased vascular endothelial cell number	Adam10<tm2Psa>/Adam10<tm2Psa>,Tg(Tek-cre)1Ywa/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	32385775
MGI:6852794	F	MP:0001729	impaired embryo implantation	Adam10<tm2Psa>/Adam10<tm2Psa>,Tg(Tek-cre)1Ywa/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	32385775
MGI:6852794	F	MP:0001926	female infertility	Adam10<tm2Psa>/Adam10<tm2Psa>,Tg(Tek-cre)1Ywa/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	32385775
MGI:6852794	F	MP:0001727	abnormal embryo implantation	Adam10<tm2Psa>/Adam10<tm2Psa>,Tg(Tek-cre)1Ywa/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	32385775
MGI:6852794	F	MP:0001923	reduced female fertility	Adam10<tm2Psa>/Adam10<tm2Psa>,Tg(Tek-cre)1Ywa/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	32385775
MGI:6852794	F	MP:0009661	abnormal pregnancy	Adam10<tm2Psa>/Adam10<tm2Psa>,Tg(Tek-cre)1Ywa/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	32385775
MGI:6852794	F	MP:0009664	abnormal luminal closure	Adam10<tm2Psa>/Adam10<tm2Psa>,Tg(Tek-cre)1Ywa/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	32385775
MGI:6852794	F	MP:0003845	abnormal decidualization	Adam10<tm2Psa>/Adam10<tm2Psa>,Tg(Tek-cre)1Ywa/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	32385775
MGI:6852794	F	MP:0009667	abnormal embryo invasion	Adam10<tm2Psa>/Adam10<tm2Psa>,Tg(Tek-cre)1Ywa/0	involves: 129P2/OlaHsd * C57BL/6 * SJL	N	32385775
MGI:6854698	M	MP:0002687	oligozoospermia	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	M	MP:0004852	decreased testis weight	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	M	MP:0003205	testicular atrophy	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	F	MP:0001127	small ovary	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21248289
MGI:6854698	M	MP:0014052	increased male germ cell apoptosis	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	F	MP:0009444	ovarian follicular cyst	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21248289
MGI:6854698	M	MP:0006380	abnormal spermatid morphology	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	F	MP:0001923	reduced female fertility	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21248289
MGI:6854698	M	MP:0001922	reduced male fertility	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	F	MP:0003507	abnormal ovary physiology	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21248289
MGI:6854698	M	MP:0020451	decreased sperm progressive motility	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	M	MP:0002675	asthenozoospermia	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	F	MP:0031420	decreased superovulation rate	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21248289
MGI:6854698	M	MP:0001156	abnormal spermatogenesis	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	M	MP:0020356	abnormal Sertoli cell barrier function	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	F	MP:0005389	reproductive system phenotype	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	Y	21248289
MGI:6854698	M	MP:0005389	reproductive system phenotype	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	Y	21172404
MGI:6854698	M	MP:0002784	abnormal Sertoli cell morphology	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	M	MP:0001147	small testis	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	M	MP:0005376	homeostasis/metabolism phenotype	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	Y	21172404
MGI:6854698	F	MP:0005418	abnormal circulating hormone level	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21248289
MGI:6854698	M	MP:0004901	decreased male germ cell number	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	M	MP:0001154	seminiferous tubule degeneration	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	M	MP:0020550	multinucleated giant male germ cells	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854698	F	MP:0001935	decreased litter size	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21248289
MGI:6854698	F	MP:0031422	failure of superovulation	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21248289
MGI:6854698	F	MP:0001926	female infertility	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21248289
MGI:6854698	F	MP:0002016	ovary cyst	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21248289
MGI:6854698	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Gata4<tm1.1Sad>/Gata4<tm1.1Sad>,Amhr2<tm3(cre)Bhr>/Amhr2<+>	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J	N	21172404
MGI:6854709	F	MP:0009671	abnormal uterus physiology	Foxa2<tm1Khk>/Foxa2<tm1Khk>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	20484741
MGI:6854709	F	MP:0003845	abnormal decidualization	Foxa2<tm1Khk>/Foxa2<tm1Khk>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	20484741
MGI:6854709	F	MP:0009667	abnormal embryo invasion	Foxa2<tm1Khk>/Foxa2<tm1Khk>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	20484741
MGI:6854709	F	MP:0001935	decreased litter size	Foxa2<tm1Khk>/Foxa2<tm1Khk>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	20484741
MGI:6854709	F	MP:0001923	reduced female fertility	Foxa2<tm1Khk>/Foxa2<tm1Khk>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	20484741
MGI:6854709	F	MP:0009096	decreased endometrial gland number	Foxa2<tm1Khk>/Foxa2<tm1Khk>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	20484741
MGI:6854709	F	MP:0001729	impaired embryo implantation	Foxa2<tm1Khk>/Foxa2<tm1Khk>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	20484741
MGI:6854709	F	MP:0013400	abnormal endometrial gland development	Foxa2<tm1Khk>/Foxa2<tm1Khk>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	20484741
MGI:6856578	F	MP:0009015	short proestrus	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856578	F	MP:0005376	homeostasis/metabolism phenotype	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	Y	21209203
MGI:6856578	F	MP:0009008	delayed estrous cycle	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856578	F	MP:0001938	delayed sexual maturation	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856578	F	MP:0001927	abnormal estrous cycle	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856578	F	MP:0001923	reduced female fertility	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856578	F	MP:0009020	prolonged metestrus	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856578	F	MP:0002773	decreased circulating luteinizing hormone level	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856578	F	MP:0008976	delayed female fertility	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856578	F	MP:0009011	prolonged diestrus	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856578	F	MP:0002680	decreased corpora lutea number	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856578	F	MP:0001935	decreased litter size	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856578	F	MP:0004856	decreased ovary weight	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856578	F	MP:0002636	delayed vaginal opening	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856578	F	MP:0003355	decreased ovulation rate	Jak2<tm1Kuw>/Jak2<tm1Kuw>,Tg(Gnrh1-cre)35Awo/0	involves: 129X1/SvJ * CD-1	N	21209203
MGI:6856673	F	MP:0008869	anovulation	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0031239	increased atretic ovarian follicle number	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0012737	abnormal primary polar body morphology	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0001127	small ovary	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0031422	failure of superovulation	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0031018	decreased granulosa cell proliferation	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0001926	female infertility	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0002682	decreased mature ovarian follicle number	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0013508	increased granulosa cell apoptosis	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0011129	decreased tertiary ovarian follicle number	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0001125	abnormal oocyte morphology	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0031420	decreased superovulation rate	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0031380	abnormal secondary ovarian follicle number	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0001129	impaired ovarian folliculogenesis	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856673	F	MP:0009761	abnormal meiotic spindle morphology	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Zp3-cre)3Mrt/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856674	F	MP:0001926	female infertility	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Gdf9-icre)5092Coo/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856674	F	MP:0031018	decreased granulosa cell proliferation	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Gdf9-icre)5092Coo/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856674	F	MP:0001129	impaired ovarian folliculogenesis	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Gdf9-icre)5092Coo/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856674	F	MP:0031383	increased secondary ovarian follicle number	Furin<tm1Jwmc>/Furin<tm1Jwmc>,Tg(Gdf9-icre)5092Coo/0	involves: 129P2/OlaHsd * C57BL/6J * CBA/J	N	28569793
MGI:6856717	M	MP:0013601	increased testis apoptosis	Pik3cb<tm1.1Ehi>/Pik3cb<tm1.1Ehi>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	20053680
MGI:6856717	M	MP:0001922	reduced male fertility	Pik3cb<tm1.1Ehi>/Pik3cb<tm1.1Ehi>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	20053680
MGI:6856717	M	MP:0006378	abnormal spermatogonia morphology	Pik3cb<tm1.1Ehi>/Pik3cb<tm1.1Ehi>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	20053680
MGI:6856717	M	MP:0005159	azoospermia	Pik3cb<tm1.1Ehi>/Pik3cb<tm1.1Ehi>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	20053680
MGI:6856717	M	MP:0002687	oligozoospermia	Pik3cb<tm1.1Ehi>/Pik3cb<tm1.1Ehi>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	20053680
MGI:6856717	M	MP:0001147	small testis	Pik3cb<tm1.1Ehi>/Pik3cb<tm1.1Ehi>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	20053680
MGI:6856717	M	MP:0011416	abnormal testis interstitial tissue morphology	Pik3cb<tm1.1Ehi>/Pik3cb<tm1.1Ehi>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	20053680
MGI:6856717	M	MP:0002216	abnormal seminiferous tubule morphology	Pik3cb<tm1.1Ehi>/Pik3cb<tm1.1Ehi>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	20053680
MGI:6856717	M	MP:0001750	increased circulating follicle stimulating hormone level	Pik3cb<tm1.1Ehi>/Pik3cb<tm1.1Ehi>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	20053680
MGI:6856717	M	MP:0004852	decreased testis weight	Pik3cb<tm1.1Ehi>/Pik3cb<tm1.1Ehi>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	20053680
MGI:6856717	M	MP:0004901	decreased male germ cell number	Pik3cb<tm1.1Ehi>/Pik3cb<tm1.1Ehi>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	20053680
MGI:6856717	M	MP:0002685	abnormal spermatogonia proliferation	Pik3cb<tm1.1Ehi>/Pik3cb<tm1.1Ehi>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	20053680
MGI:6856717	M	MP:0001156	abnormal spermatogenesis	Pik3cb<tm1.1Ehi>/Pik3cb<tm1.1Ehi>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6J	N	20053680
MGI:6856826	M	MP:0004910	decreased seminal vesicle weight	Map2k1<tm1Chrn>/Map2k1<tm1Chrn>,Map2k2<tm1Chrn>/Map2k2<tm1Chrn>,Tg(Cyp17a1-icre)AJako/0	involves: 129/Sv * C57BL/6 * C57BL/6J * SJL	N	21527500
MGI:6856826	M	MP:0001751	increased circulating luteinizing hormone level	Map2k1<tm1Chrn>/Map2k1<tm1Chrn>,Map2k2<tm1Chrn>/Map2k2<tm1Chrn>,Tg(Cyp17a1-icre)AJako/0	involves: 129/Sv * C57BL/6 * C57BL/6J * SJL	N	21527500
MGI:6856826	M	MP:0031436	decreased copulatory plug deposition	Map2k1<tm1Chrn>/Map2k1<tm1Chrn>,Map2k2<tm1Chrn>/Map2k2<tm1Chrn>,Tg(Cyp17a1-icre)AJako/0	involves: 129/Sv * C57BL/6 * C57BL/6J * SJL	N	21527500
MGI:6856826	M	MP:0001935	decreased litter size	Map2k1<tm1Chrn>/Map2k1<tm1Chrn>,Map2k2<tm1Chrn>/Map2k2<tm1Chrn>,Tg(Cyp17a1-icre)AJako/0	involves: 129/Sv * C57BL/6 * C57BL/6J * SJL	N	21527500
MGI:6856826	M	MP:0005389	reproductive system phenotype	Map2k1<tm1Chrn>/Map2k1<tm1Chrn>,Map2k2<tm1Chrn>/Map2k2<tm1Chrn>,Tg(Cyp17a1-icre)AJako/0	involves: 129/Sv * C57BL/6 * C57BL/6J * SJL	Y	21527500
MGI:6856826	M	MP:0001922	reduced male fertility	Map2k1<tm1Chrn>/Map2k1<tm1Chrn>,Map2k2<tm1Chrn>/Map2k2<tm1Chrn>,Tg(Cyp17a1-icre)AJako/0	involves: 129/Sv * C57BL/6 * C57BL/6J * SJL	N	21527500
MGI:6856826	M	MP:0014269	decreased testes secretion	Map2k1<tm1Chrn>/Map2k1<tm1Chrn>,Map2k2<tm1Chrn>/Map2k2<tm1Chrn>,Tg(Cyp17a1-icre)AJako/0	involves: 129/Sv * C57BL/6 * C57BL/6J * SJL	N	21527500
MGI:6856826	M	MP:0009819	abnormal circulating androgen level	Map2k1<tm1Chrn>/Map2k1<tm1Chrn>,Map2k2<tm1Chrn>/Map2k2<tm1Chrn>,Tg(Cyp17a1-icre)AJako/0	involves: 129/Sv * C57BL/6 * C57BL/6J * SJL	N	21527500
MGI:6856826	M	MP:0011385	abnormal testosterone level	Map2k1<tm1Chrn>/Map2k1<tm1Chrn>,Map2k2<tm1Chrn>/Map2k2<tm1Chrn>,Tg(Cyp17a1-icre)AJako/0	involves: 129/Sv * C57BL/6 * C57BL/6J * SJL	N	21527500
MGI:6856826	M	MP:0005536	decreased Leydig cell number	Map2k1<tm1Chrn>/Map2k1<tm1Chrn>,Map2k2<tm1Chrn>/Map2k2<tm1Chrn>,Tg(Cyp17a1-icre)AJako/0	involves: 129/Sv * C57BL/6 * C57BL/6J * SJL	N	21527500
MGI:6857985	M	MP:0009232	abnormal sperm nucleus morphology	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0009837	abnormal sperm end piece morphology	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0000242	impaired fertilization	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0030590	abnormal sperm fibrous sheath morphology	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0005578	teratozoospermia	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0009239	short sperm flagellum	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0020451	decreased sperm progressive motility	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0009838	abnormal sperm axoneme morphology	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0009376	abnormal manchette morphology	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0005389	reproductive system phenotype	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	Y	29236364
MGI:6857985	M	MP:0002687	oligozoospermia	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0006380	abnormal spermatid morphology	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0020869	immotile sperm	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0004182	abnormal spermiation	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0002675	asthenozoospermia	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0001932	abnormal spermiogenesis	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0031356	abnormal outer dense fiber morphology	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0009237	kinked sperm flagellum	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0001925	male infertility	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0008892	abnormal sperm flagellum morphology	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0014465	abnormal sperm mitochondrial morphology	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6857985	M	MP:0009230	abnormal sperm head morphology	Ift140<tm1c(KOMP)Wtsi>/Ift140<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N * FVB/NJ	N	29236364
MGI:6858040	M	MP:0002675	asthenozoospermia	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0008892	abnormal sperm flagellum morphology	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0020362	abnormal male germ cell physiology	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0004543	abnormal sperm physiology	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0003674	oxidative stress	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0009838	abnormal sperm axoneme morphology	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0001922	reduced male fertility	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0005578	teratozoospermia	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0004852	decreased testis weight	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0013601	increased testis apoptosis	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0001156	abnormal spermatogenesis	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0006378	abnormal spermatogonia morphology	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0002687	oligozoospermia	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858040	M	MP:0002685	abnormal spermatogonia proliferation	Rpl39l<em1Hqi>/Rpl39l<em1Hqi>	involves: C57BL/6J	N	34825148
MGI:6858076	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0031354	abnormal acrosome assembly	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0002216	abnormal seminiferous tubule morphology	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0009232	abnormal sperm nucleus morphology	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0005578	teratozoospermia	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0004852	decreased testis weight	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0031389	abnormal ectoplasmic specialization morphology	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0020869	immotile sperm	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0014052	increased male germ cell apoptosis	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0001156	abnormal spermatogenesis	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0002675	asthenozoospermia	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0002687	oligozoospermia	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0001147	small testis	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0006380	abnormal spermatid morphology	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6858076	M	MP:0001925	male infertility	Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ * SJL	N	31373619
MGI:6860339	M	MP:0009231	detached acrosome	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0009235	small sperm head	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0020451	decreased sperm progressive motility	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0009237	kinked sperm flagellum	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0006380	abnormal spermatid morphology	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0002675	asthenozoospermia	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0002687	oligozoospermia	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0001932	abnormal spermiogenesis	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0000242	impaired fertilization	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0008898	abnormal acrosome morphology	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0005578	teratozoospermia	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0009233	enlarged sperm head	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0009239	short sperm flagellum	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0030980	abnormal acroplaxome morphology	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0001925	male infertility	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0009238	coiled sperm flagellum	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0009230	abnormal sperm head morphology	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0009232	abnormal sperm nucleus morphology	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0008892	abnormal sperm flagellum morphology	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860339	M	MP:0014052	increased male germ cell apoptosis	Hipk4<tm1b(KOMP)Mbp>/Hipk4<tm1b(KOMP)Mbp>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860340	M	MP:0002675	asthenozoospermia	Hipk4<tm1b(KOMP)Mbp>/Hipk4<+>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860340	M	MP:0002687	oligozoospermia	Hipk4<tm1b(KOMP)Mbp>/Hipk4<+>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	N	32163033
MGI:6860340	M	MP:0005389	reproductive system phenotype	Hipk4<tm1b(KOMP)Mbp>/Hipk4<+>	B6N(Cg)-Hipk4<tm1b(KOMP)Mbp>/J	Y	32163033
MGI:6860531	M	MP:0009237	kinked sperm flagellum	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0030943	abnormal centrosome morphology	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0002216	abnormal seminiferous tubule morphology	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0006380	abnormal spermatid morphology	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0009838	abnormal sperm axoneme morphology	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0031386	elongated manchette	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0009831	abnormal sperm midpiece morphology	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0002687	oligozoospermia	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0002675	asthenozoospermia	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0001935	decreased litter size	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0008898	abnormal acrosome morphology	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0004543	abnormal sperm physiology	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0008892	abnormal sperm flagellum morphology	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0002662	abnormal cauda epididymis morphology	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0004182	abnormal spermiation	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0001932	abnormal spermiogenesis	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0009230	abnormal sperm head morphology	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0001922	reduced male fertility	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0005578	teratozoospermia	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0009377	ectopic manchette	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0031356	abnormal outer dense fiber morphology	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860531	M	MP:0001153	small seminiferous tubules	Ift172<tm1.1Rama>/Ift172<tm1.1Rama>,Tg(Stra8-icre)1Reb/0	involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ	N	31958312
MGI:6860681	M	MP:0002874	decreased hemoglobin content	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0011277	decreased tail pigmentation	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0030630	increased circulating methylmalonic acid level	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0005332	abnormal amino acid level	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0002875	decreased erythrocyte cell number	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0000208	decreased hematocrit	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0005352	small cranium	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0011086	postnatal lethality, incomplete penetrance	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0006411	upturned snout	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0000373	belly spot	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0005584	abnormal enzyme/coenzyme activity	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0030930	decreased digit pigmentation	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0004377	small frontal bone	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0004418	small parietal bone	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0004470	small nasal bone	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0000102	abnormal nasal bone morphology	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0001265	decreased body size	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0010499	abnormal ventricle myocardium morphology	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0001698	decreased embryo size	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0030066	short face	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0012335	increased circulating homocysteine level	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0000438	abnormal cranium morphology	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0006254	thin cerebral cortex	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6860681	M	MP:0012085	midface hypoplasia	Hcfc1<em1Poche>/Y	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:6861794	F	MP:0000562	polydactyly	Hcfc1<em1Poche>/Hcfc1<+>,Thap11<em1Poche>/Thap11<+>	C57BL/6J-Thap11<em1Poche> Hcfc1<em1Poche>	N	35013307
MGI:6861794	F	MP:0003036	vertebral transformation	Hcfc1<em1Poche>/Hcfc1<+>,Thap11<em1Poche>/Thap11<+>	C57BL/6J-Thap11<em1Poche> Hcfc1<em1Poche>	N	35013307
MGI:6861794	F	MP:0000373	belly spot	Hcfc1<em1Poche>/Hcfc1<+>,Thap11<em1Poche>/Thap11<+>	C57BL/6J-Thap11<em1Poche> Hcfc1<em1Poche>	N	35013307
MGI:6861794	F	MP:0011110	preweaning lethality, incomplete penetrance	Hcfc1<em1Poche>/Hcfc1<+>,Thap11<em1Poche>/Thap11<+>	C57BL/6J-Thap11<em1Poche> Hcfc1<em1Poche>	N	35013307
MGI:6861794	F	MP:0000102	abnormal nasal bone morphology	Hcfc1<em1Poche>/Hcfc1<+>,Thap11<em1Poche>/Thap11<+>	C57BL/6J-Thap11<em1Poche> Hcfc1<em1Poche>	N	35013307
MGI:6861794	F	MP:0000428	abnormal craniofacial morphology	Hcfc1<em1Poche>/Hcfc1<+>,Thap11<em1Poche>/Thap11<+>	C57BL/6J-Thap11<em1Poche> Hcfc1<em1Poche>	N	35013307
MGI:6861799	M	MP:0011091	prenatal lethality, complete penetrance	Hcfc1<em1Poche>/Y,Thap11<em1Poche>/Thap11<+>	C57BL/6J-Thap11<em1Poche> Hcfc1<em1Poche>	N	35013307
MGI:6861799	M	MP:0000585	kinked tail	Hcfc1<em1Poche>/Y,Thap11<em1Poche>/Thap11<+>	C57BL/6J-Thap11<em1Poche> Hcfc1<em1Poche>	N	35013307
MGI:6861799	M	MP:0003036	vertebral transformation	Hcfc1<em1Poche>/Y,Thap11<em1Poche>/Thap11<+>	C57BL/6J-Thap11<em1Poche> Hcfc1<em1Poche>	N	35013307
MGI:6861833	M	MP:0005389	reproductive system phenotype	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	Y	28964737
MGI:6861833	M	MP:0020869	immotile sperm	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0004182	abnormal spermiation	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0031351	abnormal sperm flagellum thickness	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0008279	arrest of spermiogenesis	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0001156	abnormal spermatogenesis	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0020451	decreased sperm progressive motility	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0031356	abnormal outer dense fiber morphology	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0003950	abnormal plasma membrane morphology	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0009237	kinked sperm flagellum	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0009838	abnormal sperm axoneme morphology	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0001925	male infertility	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0004884	abnormal testis physiology	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0002686	globozoospermia	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0008892	abnormal sperm flagellum morphology	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0002675	asthenozoospermia	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0014468	disorganized sperm mitochondrial sheath	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0009230	abnormal sperm head morphology	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0009239	short sperm flagellum	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0009837	abnormal sperm end piece morphology	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0005578	teratozoospermia	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0030590	abnormal sperm fibrous sheath morphology	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6861833	M	MP:0002687	oligozoospermia	Ift27<tm1c(EUCOMM)Hmgu>/Ift27<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ	N	28964737
MGI:6864067	M	MP:0004182	abnormal spermiation	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0009838	abnormal sperm axoneme morphology	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0001932	abnormal spermiogenesis	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0009237	kinked sperm flagellum	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0002687	oligozoospermia	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0008898	abnormal acrosome morphology	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0008892	abnormal sperm flagellum morphology	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0009239	short sperm flagellum	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0004884	abnormal testis physiology	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0009230	abnormal sperm head morphology	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0014468	disorganized sperm mitochondrial sheath	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0009232	abnormal sperm nucleus morphology	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0009831	abnormal sperm midpiece morphology	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0030590	abnormal sperm fibrous sheath morphology	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0002675	asthenozoospermia	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0005389	reproductive system phenotype	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	Y	32233951
MGI:6864067	M	MP:0020869	immotile sperm	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0001925	male infertility	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864067	M	MP:0020550	multinucleated giant male germ cells	Ift81<tm1c(EUCOMM)Wtsi>/Ift81<tm1c(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * C57BL/6N * FVB/NJ	N	32233951
MGI:6864146	M	MP:0020869	immotile sperm	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0005389	reproductive system phenotype	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	Y	31004481
MGI:6864146	M	MP:0031352	absent sperm axonemal central pair	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0009838	abnormal sperm axoneme morphology	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0009239	short sperm flagellum	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0006380	abnormal spermatid morphology	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0002675	asthenozoospermia	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0001925	male infertility	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0005578	teratozoospermia	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0001932	abnormal spermiogenesis	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0002216	abnormal seminiferous tubule morphology	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0009230	abnormal sperm head morphology	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0008545	absent sperm flagellum	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0004884	abnormal testis physiology	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0004182	abnormal spermiation	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864146	M	MP:0002687	oligozoospermia	Ift74<tm1c(EUCOMM)Hmgu>/Ift74<tm1c(EUCOMM)Hmgu>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ	N	31004481
MGI:6864268	M	MP:0001155	arrest of spermatogenesis	Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	24355749
MGI:6864268	M	MP:0001147	small testis	Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	24355749
MGI:6864268	M	MP:0002685	abnormal spermatogonia proliferation	Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	24355749
MGI:6864268	M	MP:0002216	abnormal seminiferous tubule morphology	Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	24355749
MGI:6864268	M	MP:0020550	multinucleated giant male germ cells	Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	24355749
MGI:6864268	M	MP:0004901	decreased male germ cell number	Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	24355749
MGI:6864268	M	MP:0002784	abnormal Sertoli cell morphology	Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	24355749
MGI:6864268	M	MP:0004852	decreased testis weight	Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	24355749
MGI:6864268	M	MP:0001154	seminiferous tubule degeneration	Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	24355749
MGI:6864268	M	MP:0004884	abnormal testis physiology	Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	24355749
MGI:6864268	M	MP:0006378	abnormal spermatogonia morphology	Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	24355749
MGI:6864268	M	MP:0005159	azoospermia	Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	24355749
MGI:6864268	M	MP:0001925	male infertility	Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	24355749
MGI:6864269	M	MP:0009239	short sperm flagellum	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	N	34792097
MGI:6864269	M	MP:0009238	coiled sperm flagellum	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	N	34792097
MGI:6864269	M	MP:0009838	abnormal sperm axoneme morphology	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	N	34792097
MGI:6864269	M	MP:0031438	abnormal sperm radial spoke morphology	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	N	34792097
MGI:6864269	M	MP:0020869	immotile sperm	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	N	34792097
MGI:6864269	M	MP:0005388	respiratory system phenotype	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	Y	34792097
MGI:6864269	M	MP:0009241	thick sperm flagellum	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	N	34792097
MGI:6864269	M	MP:0002687	oligozoospermia	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	N	34792097
MGI:6864269	M	MP:0008545	absent sperm flagellum	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	N	34792097
MGI:6864269	M	MP:0008892	abnormal sperm flagellum morphology	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	N	34792097
MGI:6864269	M	MP:0001932	abnormal spermiogenesis	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	N	34792097
MGI:6864269	M	MP:0001925	male infertility	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	N	34792097
MGI:6864269	M	MP:0009237	kinked sperm flagellum	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	N	34792097
MGI:6864269	M	MP:0005389	reproductive system phenotype	Cfap61<em1Mngx>/Cfap61<em1Mngx>	Not Specified	Y	34792097
MGI:6864286	M	MP:0005389	reproductive system phenotype	Ubl4a<tm1.1Xya>/Y,Ubl4b<em1Qsh>/Ubl4b<em1Qsh>	involves: 129	Y	34249105
MGI:6865653	F	MP:0001926	female infertility	Trp53<tm1Tyj>/Trp53<tm1Tyj>,Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	N	21277975
MGI:6865653	M	MP:0004852	decreased testis weight	Trp53<tm1Tyj>/Trp53<tm1Tyj>,Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	N	21277975
MGI:6865653	M	MP:0001154	seminiferous tubule degeneration	Trp53<tm1Tyj>/Trp53<tm1Tyj>,Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	N	21277975
MGI:6865653	M	MP:0001925	male infertility	Trp53<tm1Tyj>/Trp53<tm1Tyj>,Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	N	21277975
MGI:6865653	M	MP:0001156	abnormal spermatogenesis	Trp53<tm1Tyj>/Trp53<tm1Tyj>,Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	N	21277975
MGI:6865653	M	MP:0008995	early reproductive senescence	Trp53<tm1Tyj>/Trp53<tm1Tyj>,Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	N	21277975
MGI:6865660	F	MP:0001926	female infertility	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	FVB.129P2(B6)-Vrk1<Gt(RRR178)Byg>	N	21277975
MGI:6865660	M	MP:0001925	male infertility	Vrk1<Gt(RRR178)Byg>/Vrk1<Gt(RRR178)Byg>	FVB.129P2(B6)-Vrk1<Gt(RRR178)Byg>	N	21277975
MGI:6865740	M	MP:0002674	abnormal sperm motility	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0004182	abnormal spermiation	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0009239	short sperm flagellum	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0001156	abnormal spermatogenesis	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0005578	teratozoospermia	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0001932	abnormal spermiogenesis	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0001925	male infertility	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0002687	oligozoospermia	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0002686	globozoospermia	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0005389	reproductive system phenotype	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	Y	27682589
MGI:6865740	M	MP:0001935	decreased litter size	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0009237	kinked sperm flagellum	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0031356	abnormal outer dense fiber morphology	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0008892	abnormal sperm flagellum morphology	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0002216	abnormal seminiferous tubule morphology	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0001922	reduced male fertility	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0009838	abnormal sperm axoneme morphology	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0002675	asthenozoospermia	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865740	M	MP:0020869	immotile sperm	Ift20<tm1.1Gjp>/Ift20<tm1.2Gjp>,Tg(Stra8-icre)1Reb/0	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ	N	27682589
MGI:6865770	M	MP:0001925	male infertility	Parp6<em1Msco>/Parp6<em1Msco>	C57BL/6N-Parp6<em1Msco>	N	34067418
MGI:6865772	M	MP:0009377	ectopic manchette	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0008892	abnormal sperm flagellum morphology	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0002216	abnormal seminiferous tubule morphology	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0009239	short sperm flagellum	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0009230	abnormal sperm head morphology	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0008545	absent sperm flagellum	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0009831	abnormal sperm midpiece morphology	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0009836	abnormal sperm principal piece morphology	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0001932	abnormal spermiogenesis	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0001925	male infertility	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0009838	abnormal sperm axoneme morphology	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0020869	immotile sperm	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0030591	absent sperm fibrous sheath	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0030590	abnormal sperm fibrous sheath morphology	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	M	MP:0031356	abnormal outer dense fiber morphology	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	N	29606301
MGI:6865772	F	MP:0005389	reproductive system phenotype	Cfap69<tm1b(KOMP)Wtsi>/Cfap69<tm1b(KOMP)Wtsi>	involves: C57BL/6N	Y	29606301
MGI:6866949	M	MP:0005389	reproductive system phenotype	Spaca9<em1Osb>/Spaca9<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34471926
MGI:6866950	F	MP:0005389	reproductive system phenotype	Fam209<em2Osb>/Fam209<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34471926
MGI:6866950	M	MP:0002675	asthenozoospermia	Fam209<em2Osb>/Fam209<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34471926
MGI:6866950	M	MP:0008898	abnormal acrosome morphology	Fam209<em2Osb>/Fam209<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34471926
MGI:6866950	M	MP:0002686	globozoospermia	Fam209<em2Osb>/Fam209<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34471926
MGI:6866950	M	MP:0001925	male infertility	Fam209<em2Osb>/Fam209<em2Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34471926
MGI:6866951	M	MP:0008898	abnormal acrosome morphology	Fam209<em1Osb>/Fam209<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34471926
MGI:6866951	M	MP:0001922	reduced male fertility	Fam209<em1Osb>/Fam209<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34471926
MGI:6866951	F	MP:0005389	reproductive system phenotype	Fam209<em1Osb>/Fam209<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	34471926
MGI:6866951	M	MP:0002686	globozoospermia	Fam209<em1Osb>/Fam209<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34471926
MGI:6866951	M	MP:0002675	asthenozoospermia	Fam209<em1Osb>/Fam209<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	34471926
MGI:6867053	M	MP:0009238	coiled sperm flagellum	Akap4<em1Hqi>/Y	Not Specified	N	31969357
MGI:6867053	M	MP:0008892	abnormal sperm flagellum morphology	Akap4<em1Hqi>/Y	Not Specified	N	31969357
MGI:6867053	M	MP:0009239	short sperm flagellum	Akap4<em1Hqi>/Y	Not Specified	N	31969357
MGI:6867053	M	MP:0009836	abnormal sperm principal piece morphology	Akap4<em1Hqi>/Y	Not Specified	N	31969357
MGI:6867053	M	MP:0009282	decreased hyperactivated sperm motility	Akap4<em1Hqi>/Y	Not Specified	N	31969357
MGI:6867053	M	MP:0001925	male infertility	Akap4<em1Hqi>/Y	Not Specified	N	31969357
MGI:6867054	M	MP:0009836	abnormal sperm principal piece morphology	Akap3<em1Hqi>/Akap3<em1Hqi>	Not Specified	N	31969357
MGI:6867054	M	MP:0009239	short sperm flagellum	Akap3<em1Hqi>/Akap3<em1Hqi>	Not Specified	N	31969357
MGI:6867054	M	MP:0009282	decreased hyperactivated sperm motility	Akap3<em1Hqi>/Akap3<em1Hqi>	Not Specified	N	31969357
MGI:6867054	M	MP:0009238	coiled sperm flagellum	Akap3<em1Hqi>/Akap3<em1Hqi>	Not Specified	N	31969357
MGI:6867054	M	MP:0001925	male infertility	Akap3<em1Hqi>/Akap3<em1Hqi>	Not Specified	N	31969357
MGI:6867054	M	MP:0008892	abnormal sperm flagellum morphology	Akap3<em1Hqi>/Akap3<em1Hqi>	Not Specified	N	31969357
MGI:6867826	M	MP:0009238	coiled sperm flagellum	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0009235	small sperm head	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0009232	abnormal sperm nucleus morphology	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0008898	abnormal acrosome morphology	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0002686	globozoospermia	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0009831	abnormal sperm midpiece morphology	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0001925	male infertility	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0020869	immotile sperm	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0008839	absent acrosome	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0002687	oligozoospermia	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0001932	abnormal spermiogenesis	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0014465	abnormal sperm mitochondrial morphology	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0031355	abnormal proacrosomal vesicle fusion	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0031354	abnormal acrosome assembly	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6867826	M	MP:0002675	asthenozoospermia	AU040320<tm1b(EUCOMM)Wtsi>/AU040320<tm1b(EUCOMM)Wtsi>	involves: C57BL/6J * C57BL/6N	N	29991750
MGI:6870513	M	MP:0008898	abnormal acrosome morphology	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0001932	abnormal spermiogenesis	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0031355	abnormal proacrosomal vesicle fusion	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0002662	abnormal cauda epididymis morphology	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0004852	decreased testis weight	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0001147	small testis	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0000242	impaired fertilization	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0002686	globozoospermia	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0002687	oligozoospermia	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0014052	increased male germ cell apoptosis	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0004542	impaired acrosome reaction	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0009232	abnormal sperm nucleus morphology	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0001922	reduced male fertility	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0030940	impaired autophagy	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0002216	abnormal seminiferous tubule morphology	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870513	M	MP:0031354	abnormal acrosome assembly	Alpl<tm1(cre)Nagy>/Alpl<+>,Atg7<tm1Tchi>/Atg7<tm1Tchi>	involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	24853953
MGI:6870538	F	MP:0005376	homeostasis/metabolism phenotype	Klf5<tm1Jaw>/Klf5<tm1Jaw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	Y	22233806
MGI:6870538	F	MP:0009662	abnormal uterine receptivity	Klf5<tm1Jaw>/Klf5<tm1Jaw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	22233806
MGI:6870538	F	MP:0001935	decreased litter size	Klf5<tm1Jaw>/Klf5<tm1Jaw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	22233806
MGI:6870538	F	MP:0009666	abnormal embryo attachment	Klf5<tm1Jaw>/Klf5<tm1Jaw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	22233806
MGI:6870538	F	MP:0001926	female infertility	Klf5<tm1Jaw>/Klf5<tm1Jaw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	22233806
MGI:6870538	F	MP:0003845	abnormal decidualization	Klf5<tm1Jaw>/Klf5<tm1Jaw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	22233806
MGI:6870538	F	MP:0001729	impaired embryo implantation	Klf5<tm1Jaw>/Klf5<tm1Jaw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	22233806
MGI:6870538	F	MP:0001728	failure of embryo implantation	Klf5<tm1Jaw>/Klf5<tm1Jaw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	22233806
MGI:6870538	F	MP:0001923	reduced female fertility	Klf5<tm1Jaw>/Klf5<tm1Jaw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	22233806
MGI:6872282	M	MP:0020869	immotile sperm	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0001935	decreased litter size	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0030978	impaired binding of sperm to zona pellucida	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0002675	asthenozoospermia	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	30606959
MGI:6872282	M	MP:0001922	reduced male fertility	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0031354	abnormal acrosome assembly	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0009282	decreased hyperactivated sperm motility	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0008898	abnormal acrosome morphology	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0009647	decreased fertilization frequency	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0009232	abnormal sperm nucleus morphology	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0001932	abnormal spermiogenesis	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0001925	male infertility	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0031009	abnormal sperm-egg fusion	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0020451	decreased sperm progressive motility	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0009831	abnormal sperm midpiece morphology	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0020451	decreased sperm progressive motility	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	30606959
MGI:6872282	M	MP:0002675	asthenozoospermia	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0031012	impaired sperm migration in female genital tract	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	30606959
MGI:6872282	M	MP:0002674	abnormal sperm motility	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	30606959
MGI:6872282	M	MP:0002674	abnormal sperm motility	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6872282	M	MP:0002686	globozoospermia	Acrbp<tm1Tba>/Acrbp<tm1Tba>	involves: 129S2/SvPas * ICR	N	27303034
MGI:6874588	M	MP:0009830	abnormal sperm connecting piece morphology	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	29663073
MGI:6874588	M	MP:0001925	male infertility	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	29663073
MGI:6874588	M	MP:0009377	ectopic manchette	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	29663073
MGI:6874588	M	MP:0008898	abnormal acrosome morphology	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	29663073
MGI:6874588	M	MP:0006380	abnormal spermatid morphology	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	29663073
MGI:6874588	M	MP:0009376	abnormal manchette morphology	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	29663073
MGI:6874588	M	MP:0002686	globozoospermia	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	29663073
MGI:6874588	M	MP:0001932	abnormal spermiogenesis	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	29663073
MGI:6874588	M	MP:0031356	abnormal outer dense fiber morphology	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	29663073
MGI:6874588	M	MP:0009836	abnormal sperm principal piece morphology	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	29663073
MGI:6874588	F	MP:0005389	reproductive system phenotype	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	Y	29663073
MGI:6874588	M	MP:0009232	abnormal sperm nucleus morphology	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	29663073
MGI:6874588	M	MP:0002687	oligozoospermia	Spag4<tm1(KOMP)Mbp>/Spag4<tm1(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	29663073
MGI:6879433	M	MP:0002675	asthenozoospermia	Lrrc23<em1Mngx>/Lrrc23<em1Mngx>	involves: C57BL/6 * DBA/2	N	34585727
MGI:6879433	M	MP:0020451	decreased sperm progressive motility	Lrrc23<em1Mngx>/Lrrc23<em1Mngx>	involves: C57BL/6 * DBA/2	N	34585727
MGI:6879433	M	MP:0009838	abnormal sperm axoneme morphology	Lrrc23<em1Mngx>/Lrrc23<em1Mngx>	involves: C57BL/6 * DBA/2	N	34585727
MGI:6879433	M	MP:0031438	abnormal sperm radial spoke morphology	Lrrc23<em1Mngx>/Lrrc23<em1Mngx>	involves: C57BL/6 * DBA/2	N	34585727
MGI:6879433	M	MP:0001925	male infertility	Lrrc23<em1Mngx>/Lrrc23<em1Mngx>	involves: C57BL/6 * DBA/2	N	34585727
MGI:6879433	M	MP:0005388	respiratory system phenotype	Lrrc23<em1Mngx>/Lrrc23<em1Mngx>	involves: C57BL/6 * DBA/2	Y	34585727
MGI:6879433	M	MP:0000242	impaired fertilization	Lrrc23<em1Mngx>/Lrrc23<em1Mngx>	involves: C57BL/6 * DBA/2	N	34585727
MGI:6879435	M	MP:0020451	decreased sperm progressive motility	Lrrc23<em2Mngx>/Lrrc23<em2Mngx>	involves: C57BL/6 * DBA/2	N	34585727
MGI:6879435	M	MP:0001925	male infertility	Lrrc23<em2Mngx>/Lrrc23<em2Mngx>	involves: C57BL/6 * DBA/2	N	34585727
MGI:6879435	M	MP:0031438	abnormal sperm radial spoke morphology	Lrrc23<em2Mngx>/Lrrc23<em2Mngx>	involves: C57BL/6 * DBA/2	N	34585727
MGI:6879435	M	MP:0002675	asthenozoospermia	Lrrc23<em2Mngx>/Lrrc23<em2Mngx>	involves: C57BL/6 * DBA/2	N	34585727
MGI:6879439	M	MP:0002675	asthenozoospermia	Lrrc23<em1Mngx>/Lrrc23<em1Mngx>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: C57BL/6 * DBA/2	N	34585727
MGI:6883592	M	MP:0001932	abnormal spermiogenesis	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0002662	abnormal cauda epididymis morphology	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0031354	abnormal acrosome assembly	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0030591	absent sperm fibrous sheath	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0031372	abnormal sperm individualization	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0009232	abnormal sperm nucleus morphology	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0001922	reduced male fertility	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0001925	male infertility	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0004852	decreased testis weight	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0005578	teratozoospermia	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0030940	impaired autophagy	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0004884	abnormal testis physiology	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0009239	short sperm flagellum	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0008892	abnormal sperm flagellum morphology	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0002686	globozoospermia	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0020869	immotile sperm	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0009831	abnormal sperm midpiece morphology	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0009837	abnormal sperm end piece morphology	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0002675	asthenozoospermia	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0031409	double-headed sperm	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0002687	oligozoospermia	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0009230	abnormal sperm head morphology	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0020550	multinucleated giant male germ cells	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6883592	M	MP:0004182	abnormal spermiation	Atg5<tm1Myok>/Atg5<tm1Myok>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * FVB/NJ	N	32677505
MGI:6885538	M	MP:0005670	abnormal white adipose tissue physiology	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885538	M	MP:0005376	homeostasis/metabolism phenotype	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	Y	28357399
MGI:6885538	M	MP:0002781	increased circulating testosterone level	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885538	M	MP:0001925	male infertility	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885538	M	MP:0003953	abnormal hormone level	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885538	M	MP:0001938	delayed sexual maturation	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885538	M	MP:0004884	abnormal testis physiology	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885538	M	MP:0004852	decreased testis weight	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885538	M	MP:0005189	abnormal anogenital distance	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885538	M	MP:0009819	abnormal circulating androgen level	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885538	M	MP:0005669	increased circulating leptin level	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885538	M	MP:0010024	increased total body fat amount	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885538	M	MP:0002773	decreased circulating luteinizing hormone level	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885538	M	MP:0008940	delayed balanopreputial separation	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885538	M	MP:0001260	increased body weight	Pik3ca<tm1.1Rzl>/Pik3ca<tm1.1Rzl>,Tg(Fabp4-cre)1Blw/0	involves: 129 * C57BL/6 * FVB/N	N	28357399
MGI:6885740	M	MP:0009831	abnormal sperm midpiece morphology	Hsp90b1<tm1Zhli>/Hsp90b1<tm1.1Zhli>,Tg(Ddx4-cre)1Dcas/0	involves: 129S/SvEv * FVB	N	21208614
MGI:6885740	M	MP:0002675	asthenozoospermia	Hsp90b1<tm1Zhli>/Hsp90b1<tm1.1Zhli>,Tg(Ddx4-cre)1Dcas/0	involves: 129S/SvEv * FVB	N	21208614
MGI:6885740	M	MP:0008898	abnormal acrosome morphology	Hsp90b1<tm1Zhli>/Hsp90b1<tm1.1Zhli>,Tg(Ddx4-cre)1Dcas/0	involves: 129S/SvEv * FVB	N	21208614
MGI:6885740	M	MP:0009233	enlarged sperm head	Hsp90b1<tm1Zhli>/Hsp90b1<tm1.1Zhli>,Tg(Ddx4-cre)1Dcas/0	involves: 129S/SvEv * FVB	N	21208614
MGI:6885740	M	MP:0009230	abnormal sperm head morphology	Hsp90b1<tm1Zhli>/Hsp90b1<tm1.1Zhli>,Tg(Ddx4-cre)1Dcas/0	involves: 129S/SvEv * FVB	N	21208614
MGI:6885740	M	MP:0005389	reproductive system phenotype	Hsp90b1<tm1Zhli>/Hsp90b1<tm1.1Zhli>,Tg(Ddx4-cre)1Dcas/0	involves: 129S/SvEv * FVB	Y	21208614
MGI:6885740	M	MP:0002686	globozoospermia	Hsp90b1<tm1Zhli>/Hsp90b1<tm1.1Zhli>,Tg(Ddx4-cre)1Dcas/0	involves: 129S/SvEv * FVB	N	21208614
MGI:6885740	M	MP:0001925	male infertility	Hsp90b1<tm1Zhli>/Hsp90b1<tm1.1Zhli>,Tg(Ddx4-cre)1Dcas/0	involves: 129S/SvEv * FVB	N	21208614
MGI:6885771	M	MP:0006380	abnormal spermatid morphology	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129 * C57BL/6	N	12784252
MGI:6885771	M	MP:0030590	abnormal sperm fibrous sheath morphology	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129 * C57BL/6	N	12784252
MGI:6885771	M	MP:0009376	abnormal manchette morphology	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129 * C57BL/6	N	12784252
MGI:6885771	M	MP:0009377	ectopic manchette	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129 * C57BL/6	N	12784252
MGI:6885771	M	MP:0008892	abnormal sperm flagellum morphology	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129 * C57BL/6	N	12784252
MGI:6885878	M	MP:0004852	decreased testis weight	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0001147	small testis	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0020869	immotile sperm	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0009230	abnormal sperm head morphology	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0009833	absent sperm mitochondrial sheath	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0001925	male infertility	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0002686	globozoospermia	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0031354	abnormal acrosome assembly	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0006380	abnormal spermatid morphology	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0031355	abnormal proacrosomal vesicle fusion	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0001932	abnormal spermiogenesis	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0020378	abnormal cell cytoskeleton morphology	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0020849	abnormal actin cytoskeleton morphology	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0008839	absent acrosome	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0011743	abnormal Golgi apparatus morphology	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0020850	abnormal microtubule cytoskeleton morphology	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0009232	abnormal sperm nucleus morphology	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0001262	decreased body weight	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0020451	decreased sperm progressive motility	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885878	M	MP:0002687	oligozoospermia	Golga2<tm1.2Baos>/Golga2<tm1.2Baos>	involves: 129 * C57BL/6	N	28055014
MGI:6885893	M	MP:0009232	abnormal sperm nucleus morphology	Golga2<tm1.1Baos>/Golga2<tm1.2Baos>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ	N	28055014
MGI:6885893	M	MP:0009230	abnormal sperm head morphology	Golga2<tm1.1Baos>/Golga2<tm1.2Baos>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ	N	28055014
MGI:6885893	M	MP:0009833	absent sperm mitochondrial sheath	Golga2<tm1.1Baos>/Golga2<tm1.2Baos>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ	N	28055014
MGI:6885893	M	MP:0001932	abnormal spermiogenesis	Golga2<tm1.1Baos>/Golga2<tm1.2Baos>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ	N	28055014
MGI:6885893	M	MP:0008839	absent acrosome	Golga2<tm1.1Baos>/Golga2<tm1.2Baos>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ	N	28055014
MGI:6885893	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Golga2<tm1.1Baos>/Golga2<tm1.2Baos>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ	N	28055014
MGI:6885893	M	MP:0001925	male infertility	Golga2<tm1.1Baos>/Golga2<tm1.2Baos>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ	N	28055014
MGI:6885893	M	MP:0002686	globozoospermia	Golga2<tm1.1Baos>/Golga2<tm1.2Baos>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ	N	28055014
MGI:6886231	M	MP:0005378	growth/size/body region phenotype	P2rx2<em1Xzl>/P2rx2<+>	CBA/J-P2rx2<em1Xzl>	Y	33791800
MGI:6886231	M	MP:0001405	impaired coordination	P2rx2<em1Xzl>/P2rx2<+>	CBA/J-P2rx2<em1Xzl>	N	33791800
MGI:6886231	M	MP:0010771	integument phenotype	P2rx2<em1Xzl>/P2rx2<+>	CBA/J-P2rx2<em1Xzl>	Y	33791800
MGI:6886231	M	MP:0011967	increased or absent threshold for auditory brainstem response	P2rx2<em1Xzl>/P2rx2<+>	CBA/J-P2rx2<em1Xzl>	N	33791800
MGI:6886231	M	MP:0005386	behavior/neurological phenotype	P2rx2<em1Xzl>/P2rx2<+>	CBA/J-P2rx2<em1Xzl>	Y	33791800
MGI:6886231	F	MP:0011967	increased or absent threshold for auditory brainstem response	P2rx2<em1Xzl>/P2rx2<+>	CBA/J-P2rx2<em1Xzl>	N	33791800
MGI:6887367	M	MP:0002686	globozoospermia	Slc9a8<tm1d(KOMP)Wtsi>/Slc9a8<tm1d(KOMP)Wtsi>	involves: C57BL/6N	N	28476888
MGI:6887367	M	MP:0009833	absent sperm mitochondrial sheath	Slc9a8<tm1d(KOMP)Wtsi>/Slc9a8<tm1d(KOMP)Wtsi>	involves: C57BL/6N	N	28476888
MGI:6887367	M	MP:0009232	abnormal sperm nucleus morphology	Slc9a8<tm1d(KOMP)Wtsi>/Slc9a8<tm1d(KOMP)Wtsi>	involves: C57BL/6N	N	28476888
MGI:6887367	M	MP:0008839	absent acrosome	Slc9a8<tm1d(KOMP)Wtsi>/Slc9a8<tm1d(KOMP)Wtsi>	involves: C57BL/6N	N	28476888
MGI:6887367	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Slc9a8<tm1d(KOMP)Wtsi>/Slc9a8<tm1d(KOMP)Wtsi>	involves: C57BL/6N	N	28476888
MGI:6887367	M	MP:0005389	reproductive system phenotype	Slc9a8<tm1d(KOMP)Wtsi>/Slc9a8<tm1d(KOMP)Wtsi>	involves: C57BL/6N	Y	28476888
MGI:6887367	M	MP:0031355	abnormal proacrosomal vesicle fusion	Slc9a8<tm1d(KOMP)Wtsi>/Slc9a8<tm1d(KOMP)Wtsi>	involves: C57BL/6N	N	28476888
MGI:6887367	M	MP:0031354	abnormal acrosome assembly	Slc9a8<tm1d(KOMP)Wtsi>/Slc9a8<tm1d(KOMP)Wtsi>	involves: C57BL/6N	N	28476888
MGI:6887367	M	MP:0002675	asthenozoospermia	Slc9a8<tm1d(KOMP)Wtsi>/Slc9a8<tm1d(KOMP)Wtsi>	involves: C57BL/6N	N	28476888
MGI:6887367	M	MP:0001925	male infertility	Slc9a8<tm1d(KOMP)Wtsi>/Slc9a8<tm1d(KOMP)Wtsi>	involves: C57BL/6N	N	28476888
MGI:6887369	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Slc9a8<tm1d(KOMP)Wtsi>/Slc9a8<tm1d(KOMP)Wtsi>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: C57BL/6 * C57BL/6N * DBA/2	N	28476888
MGI:6887369	M	MP:0008839	absent acrosome	Slc9a8<tm1d(KOMP)Wtsi>/Slc9a8<tm1d(KOMP)Wtsi>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: C57BL/6 * C57BL/6N * DBA/2	N	28476888
MGI:6887369	M	MP:0009833	absent sperm mitochondrial sheath	Slc9a8<tm1d(KOMP)Wtsi>/Slc9a8<tm1d(KOMP)Wtsi>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: C57BL/6 * C57BL/6N * DBA/2	N	28476888
MGI:6887370	M	MP:0005389	reproductive system phenotype	Slc9a8<tm1c(KOMP)Wtsi>/Slc9a8<tm1c(KOMP)Wtsi>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6N	Y	28476888
MGI:6887371	M	MP:0008839	absent acrosome	Slc9a8<tm1c(KOMP)Wtsi>/Slc9a8<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N * FVB/NJ	N	28476888
MGI:6887371	M	MP:0002686	globozoospermia	Slc9a8<tm1c(KOMP)Wtsi>/Slc9a8<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N * FVB/NJ	N	28476888
MGI:6887371	M	MP:0009230	abnormal sperm head morphology	Slc9a8<tm1c(KOMP)Wtsi>/Slc9a8<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N * FVB/NJ	N	28476888
MGI:6887371	M	MP:0031355	abnormal proacrosomal vesicle fusion	Slc9a8<tm1c(KOMP)Wtsi>/Slc9a8<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N * FVB/NJ	N	28476888
MGI:6887371	M	MP:0031354	abnormal acrosome assembly	Slc9a8<tm1c(KOMP)Wtsi>/Slc9a8<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N * FVB/NJ	N	28476888
MGI:6887371	M	MP:0001925	male infertility	Slc9a8<tm1c(KOMP)Wtsi>/Slc9a8<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N * FVB/NJ	N	28476888
MGI:6887371	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Slc9a8<tm1c(KOMP)Wtsi>/Slc9a8<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N * FVB/NJ	N	28476888
MGI:6887371	M	MP:0005389	reproductive system phenotype	Slc9a8<tm1c(KOMP)Wtsi>/Slc9a8<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N * FVB/NJ	Y	28476888
MGI:6887371	M	MP:0009833	absent sperm mitochondrial sheath	Slc9a8<tm1c(KOMP)Wtsi>/Slc9a8<tm1c(KOMP)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * C57BL/6N * FVB/NJ	N	28476888
MGI:6887458	M	MP:0002675	asthenozoospermia	Septin12<tm3Plk>/Septin12<+>	involves: 129 * C57BL/6	N	25588830
MGI:6887458	M	MP:0005389	reproductive system phenotype	Septin12<tm3Plk>/Septin12<+>	involves: 129 * C57BL/6	Y	25588830
MGI:6887459	M	MP:0009834	abnormal sperm annulus morphology	Septin12<tm3Plk>/Septin12<tm3Plk>	involves: 129 * C57BL/6	N	25588830
MGI:6887459	M	MP:0002675	asthenozoospermia	Septin12<tm3Plk>/Septin12<tm3Plk>	involves: 129 * C57BL/6	N	25588830
MGI:6887459	M	MP:0005389	reproductive system phenotype	Septin12<tm3Plk>/Septin12<tm3Plk>	involves: 129 * C57BL/6	Y	25588830
MGI:6887459	M	MP:0009237	kinked sperm flagellum	Septin12<tm3Plk>/Septin12<tm3Plk>	involves: 129 * C57BL/6	N	25588830
MGI:6887459	M	MP:0008892	abnormal sperm flagellum morphology	Septin12<tm3Plk>/Septin12<tm3Plk>	involves: 129 * C57BL/6	N	25588830
MGI:6887596	M	MP:0031386	elongated manchette	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0004929	decreased epididymis weight	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0009230	abnormal sperm head morphology	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0009232	abnormal sperm nucleus morphology	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0014468	disorganized sperm mitochondrial sheath	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0009838	abnormal sperm axoneme morphology	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0008892	abnormal sperm flagellum morphology	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0009376	abnormal manchette morphology	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0001925	male infertility	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0002631	abnormal epididymis morphology	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0006380	abnormal spermatid morphology	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0004852	decreased testis weight	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0009377	ectopic manchette	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0001156	abnormal spermatogenesis	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0002662	abnormal cauda epididymis morphology	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0002687	oligozoospermia	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0031375	abnormal manchette disassembly	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0031356	abnormal outer dense fiber morphology	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0031373	abnormal manchette perinuclear ring morphology	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887596	M	MP:0030590	abnormal sperm fibrous sheath morphology	Kif3a<tm2Gsn>/Kif3a<tm2Gsn>,Tg(NEUROG3-cre)1Herr/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	23831641
MGI:6887647	M	MP:0009242	thin sperm flagellum	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0008892	abnormal sperm flagellum morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0004901	decreased male germ cell number	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0001925	male infertility	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0011743	abnormal Golgi apparatus morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0030591	absent sperm fibrous sheath	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0009235	small sperm head	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0009230	abnormal sperm head morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0009236	pinhead sperm	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0014052	increased male germ cell apoptosis	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0009237	kinked sperm flagellum	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0009232	abnormal sperm nucleus morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0005578	teratozoospermia	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0009376	abnormal manchette morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0009833	absent sperm mitochondrial sheath	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0006380	abnormal spermatid morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0008898	abnormal acrosome morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0009377	ectopic manchette	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0002631	abnormal epididymis morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0002687	oligozoospermia	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0009831	abnormal sperm midpiece morphology	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0001932	abnormal spermiogenesis	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887647	M	MP:0001147	small testis	Dicer1<tm1Bdh>/Dicer1<tm1Bdh>,Tg(NEUROG3-cre)1Herr/0	involves: 129 * C57BL/6J	N	21949761
MGI:6887744	M	MP:0001155	arrest of spermatogenesis	Gt(ROSA)26Sor<tm1(cre/ERT2)Thl>/Gt(ROSA)26Sor<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887744	M	MP:0005389	reproductive system phenotype	Gt(ROSA)26Sor<tm1(cre/ERT2)Thl>/Gt(ROSA)26Sor<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	Y	29293683
MGI:6887744	M	MP:0001154	seminiferous tubule degeneration	Gt(ROSA)26Sor<tm1(cre/ERT2)Thl>/Gt(ROSA)26Sor<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887744	M	MP:0006378	abnormal spermatogonia morphology	Gt(ROSA)26Sor<tm1(cre/ERT2)Thl>/Gt(ROSA)26Sor<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887744	M	MP:0013601	increased testis apoptosis	Gt(ROSA)26Sor<tm1(cre/ERT2)Thl>/Gt(ROSA)26Sor<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887744	M	MP:0004901	decreased male germ cell number	Gt(ROSA)26Sor<tm1(cre/ERT2)Thl>/Gt(ROSA)26Sor<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887744	M	MP:0005159	azoospermia	Gt(ROSA)26Sor<tm1(cre/ERT2)Thl>/Gt(ROSA)26Sor<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887746	M	MP:0006378	abnormal spermatogonia morphology	Alpl<tm1(cre)Nagy>/Alpl<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887746	M	MP:0004852	decreased testis weight	Alpl<tm1(cre)Nagy>/Alpl<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887746	M	MP:0004901	decreased male germ cell number	Alpl<tm1(cre)Nagy>/Alpl<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887746	M	MP:0002685	abnormal spermatogonia proliferation	Alpl<tm1(cre)Nagy>/Alpl<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887746	M	MP:0005159	azoospermia	Alpl<tm1(cre)Nagy>/Alpl<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887746	M	MP:0001147	small testis	Alpl<tm1(cre)Nagy>/Alpl<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887746	M	MP:0014052	increased male germ cell apoptosis	Alpl<tm1(cre)Nagy>/Alpl<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887746	M	MP:0001155	arrest of spermatogenesis	Alpl<tm1(cre)Nagy>/Alpl<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887746	M	MP:0001154	seminiferous tubule degeneration	Alpl<tm1(cre)Nagy>/Alpl<+>,Pknox1<tm1.1Rygo>/Pknox1<tm1.1Rygo>	involves: 129 * C57BL/6 * C57BL/6JJcl	N	29293683
MGI:6887872	M	MP:0001932	abnormal spermiogenesis	Iqcg<tm1a(EUCOMM)Wtsi>/Iqcg<tm1a(EUCOMM)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24849454
MGI:6887872	M	MP:0008892	abnormal sperm flagellum morphology	Iqcg<tm1a(EUCOMM)Wtsi>/Iqcg<tm1a(EUCOMM)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24849454
MGI:6887872	M	MP:0009239	short sperm flagellum	Iqcg<tm1a(EUCOMM)Wtsi>/Iqcg<tm1a(EUCOMM)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24849454
MGI:6887872	M	MP:0002662	abnormal cauda epididymis morphology	Iqcg<tm1a(EUCOMM)Wtsi>/Iqcg<tm1a(EUCOMM)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24849454
MGI:6887872	M	MP:0009232	abnormal sperm nucleus morphology	Iqcg<tm1a(EUCOMM)Wtsi>/Iqcg<tm1a(EUCOMM)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24849454
MGI:6887872	M	MP:0009838	abnormal sperm axoneme morphology	Iqcg<tm1a(EUCOMM)Wtsi>/Iqcg<tm1a(EUCOMM)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24849454
MGI:6887872	M	MP:0001925	male infertility	Iqcg<tm1a(EUCOMM)Wtsi>/Iqcg<tm1a(EUCOMM)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24849454
MGI:6887872	M	MP:0009230	abnormal sperm head morphology	Iqcg<tm1a(EUCOMM)Wtsi>/Iqcg<tm1a(EUCOMM)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24849454
MGI:6887872	M	MP:0020869	immotile sperm	Iqcg<tm1a(EUCOMM)Wtsi>/Iqcg<tm1a(EUCOMM)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24849454
MGI:6887872	M	MP:0002660	abnormal caput epididymis morphology	Iqcg<tm1a(EUCOMM)Wtsi>/Iqcg<tm1a(EUCOMM)Wtsi>	involves: C57BL/6 * C57BL/6N	N	24849454
MGI:6887874	M	MP:0005389	reproductive system phenotype	Mettl21a<em1Syu>/Mettl21a<em1Syu>	involves: C57BL/6J * CBA/J	Y	35216057
MGI:6887927	M	MP:0002216	abnormal seminiferous tubule morphology	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0005578	teratozoospermia	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0009230	abnormal sperm head morphology	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0009833	absent sperm mitochondrial sheath	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0002660	abnormal caput epididymis morphology	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0002662	abnormal cauda epididymis morphology	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0009231	detached acrosome	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0031375	abnormal manchette disassembly	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0008545	absent sperm flagellum	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0001925	male infertility	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0006380	abnormal spermatid morphology	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0009838	abnormal sperm axoneme morphology	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0031374	abnormal manchette assembly	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0009239	short sperm flagellum	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0031373	abnormal manchette perinuclear ring morphology	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0002687	oligozoospermia	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0030590	abnormal sperm fibrous sheath morphology	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0001932	abnormal spermiogenesis	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887927	M	MP:0009376	abnormal manchette morphology	Agbl5<tm1.2Ics>/Agbl5<tm1.2Ics>	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887929	M	MP:0002216	abnormal seminiferous tubule morphology	Agbl5<tm1.1Ics>/Agbl5<tm1.1Ics>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887929	M	MP:0005389	reproductive system phenotype	Agbl5<tm1.1Ics>/Agbl5<tm1.1Ics>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPas * C57BL/6N	Y	30635446
MGI:6887929	M	MP:0009231	detached acrosome	Agbl5<tm1.1Ics>/Agbl5<tm1.1Ics>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887929	M	MP:0001932	abnormal spermiogenesis	Agbl5<tm1.1Ics>/Agbl5<tm1.1Ics>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887929	M	MP:0002687	oligozoospermia	Agbl5<tm1.1Ics>/Agbl5<tm1.1Ics>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887929	M	MP:0031373	abnormal manchette perinuclear ring morphology	Agbl5<tm1.1Ics>/Agbl5<tm1.1Ics>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887929	M	MP:0009838	abnormal sperm axoneme morphology	Agbl5<tm1.1Ics>/Agbl5<tm1.1Ics>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887929	M	MP:0009243	hairpin sperm flagellum	Agbl5<tm1.1Ics>/Agbl5<tm1.1Ics>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887929	M	MP:0006380	abnormal spermatid morphology	Agbl5<tm1.1Ics>/Agbl5<tm1.1Ics>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887929	M	MP:0009232	abnormal sperm nucleus morphology	Agbl5<tm1.1Ics>/Agbl5<tm1.1Ics>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887929	M	MP:0002662	abnormal cauda epididymis morphology	Agbl5<tm1.1Ics>/Agbl5<tm1.1Ics>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6887929	M	MP:0031374	abnormal manchette assembly	Agbl5<tm1.1Ics>/Agbl5<tm1.1Ics>,Tg(Stra8-icre)1Reb/0	involves: 129S2/SvPas * C57BL/6N	N	30635446
MGI:6888114	M	MP:0020550	multinucleated giant male germ cells	Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Stra8-icre)1Reb/0	involves: 129S1/Sv * 129X1/SvJ * FVB/NJ	N	29386567
MGI:6888114	M	MP:0006380	abnormal spermatid morphology	Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Stra8-icre)1Reb/0	involves: 129S1/Sv * 129X1/SvJ * FVB/NJ	N	29386567
MGI:6888114	M	MP:0005159	azoospermia	Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Stra8-icre)1Reb/0	involves: 129S1/Sv * 129X1/SvJ * FVB/NJ	N	29386567
MGI:6888114	M	MP:0001925	male infertility	Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Stra8-icre)1Reb/0	involves: 129S1/Sv * 129X1/SvJ * FVB/NJ	N	29386567
MGI:6888114	M	MP:0001155	arrest of spermatogenesis	Mgat1<tm2Jxm>/Mgat1<tm2Jxm>,Tg(Stra8-icre)1Reb/0	involves: 129S1/Sv * 129X1/SvJ * FVB/NJ	N	29386567
MGI:6888119	M	MP:0004852	decreased testis weight	Rad51ap2<em1Qsh>/Rad51ap2<em1Qsh>	involves: C57BL/6J * DBA/2J	N	35020426
MGI:6888119	F	MP:0005389	reproductive system phenotype	Rad51ap2<em1Qsh>/Rad51ap2<em1Qsh>	involves: C57BL/6J * DBA/2J	Y	35020426
MGI:6888119	M	MP:0002687	oligozoospermia	Rad51ap2<em1Qsh>/Rad51ap2<em1Qsh>	involves: C57BL/6J * DBA/2J	N	35020426
MGI:6888119	M	MP:0014052	increased male germ cell apoptosis	Rad51ap2<em1Qsh>/Rad51ap2<em1Qsh>	involves: C57BL/6J * DBA/2J	N	35020426
MGI:6888119	M	MP:0008261	arrest of male meiosis	Rad51ap2<em1Qsh>/Rad51ap2<em1Qsh>	involves: C57BL/6J * DBA/2J	N	35020426
MGI:6888119	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Rad51ap2<em1Qsh>/Rad51ap2<em1Qsh>	involves: C57BL/6J * DBA/2J	N	35020426
MGI:6888120	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Rad51ap2<em2Qsh>/Rad51ap2<em2Qsh>	involves: C57BL/6J * DBA/2J	N	35020426
MGI:7255036	F	MP:0001402	decreased locomotor activity	Atp5if1<em1Jpy>/Atp5if1<em1Jpy>	C57BL/6J-Atp5if1<em1Jpy>	N	34221868
MGI:7255036	F	MP:0000495	abnormal colon morphology	Atp5if1<em1Jpy>/Atp5if1<em1Jpy>	C57BL/6J-Atp5if1<em1Jpy>	N	34221868
MGI:7255036	M	MP:0005658	increased susceptibility to diet-induced obesity	Atp5if1<em1Jpy>/Atp5if1<em1Jpy>	C57BL/6J-Atp5if1<em1Jpy>	N	34221868
MGI:7255036	M	MP:0009288	increased epididymal fat pad weight	Atp5if1<em1Jpy>/Atp5if1<em1Jpy>	C57BL/6J-Atp5if1<em1Jpy>	N	34221868
MGI:7255036	F	MP:0014046	abnormal mitophagy	Atp5if1<em1Jpy>/Atp5if1<em1Jpy>	C57BL/6J-Atp5if1<em1Jpy>	N	34221868
MGI:7255036	F	MP:0005292	improved glucose tolerance	Atp5if1<em1Jpy>/Atp5if1<em1Jpy>	C57BL/6J-Atp5if1<em1Jpy>	N	34221868
MGI:7255036	F	MP:0002981	increased liver weight	Atp5if1<em1Jpy>/Atp5if1<em1Jpy>	C57BL/6J-Atp5if1<em1Jpy>	N	34221868
MGI:7255036	F	MP:0011637	abnormal mitochondrial matrix morphology	Atp5if1<em1Jpy>/Atp5if1<em1Jpy>	C57BL/6J-Atp5if1<em1Jpy>	N	34221868
MGI:7255036	F	MP:0000479	abnormal enterocyte morphology	Atp5if1<em1Jpy>/Atp5if1<em1Jpy>	C57BL/6J-Atp5if1<em1Jpy>	N	34221868
MGI:7255036	F	MP:0005331	insulin resistance	Atp5if1<em1Jpy>/Atp5if1<em1Jpy>	C57BL/6J-Atp5if1<em1Jpy>	N	34221868
MGI:7255036	F	MP:0014234	decreased enterocyte apoptosis	Atp5if1<em1Jpy>/Atp5if1<em1Jpy>	C57BL/6J-Atp5if1<em1Jpy>	N	34221868
MGI:7255036	F	MP:0011631	decreased mitochondrial size	Atp5if1<em1Jpy>/Atp5if1<em1Jpy>	C57BL/6J-Atp5if1<em1Jpy>	N	34221868
MGI:7255036	F	MP:0004890	decreased energy expenditure	Atp5if1<em1Jpy>/Atp5if1<em1Jpy>	C57BL/6J-Atp5if1<em1Jpy>	N	34221868
MGI:7256335	M	MP:0005179	decreased circulating cholesterol level	Agmo<tm2a(EUCOMM)Wtsi>/Agmo<tm2a(EUCOMM)Wtsi>	involves: C57BL/6N	N	33726865
MGI:7256336	M	MP:0014052	increased male germ cell apoptosis	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0001147	small testis	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0001925	male infertility	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0009232	abnormal sperm nucleus morphology	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0020869	immotile sperm	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0002686	globozoospermia	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0002675	asthenozoospermia	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0005578	teratozoospermia	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0031354	abnormal acrosome assembly	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0031355	abnormal proacrosomal vesicle fusion	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0005376	homeostasis/metabolism phenotype	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	Y	23052838
MGI:7256336	M	MP:0002687	oligozoospermia	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0009230	abnormal sperm head morphology	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0006380	abnormal spermatid morphology	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0002216	abnormal seminiferous tubule morphology	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	M	MP:0001932	abnormal spermiogenesis	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	N	23052838
MGI:7256336	F	MP:0005389	reproductive system phenotype	Galnt3<tm1Tok>/Galnt3<tm1Tok>	involves: 129P2/OlaHsd * C57BL/6	Y	23052838
MGI:7256401	M	MP:0001860	liver inflammation	Hsd17b13<tm1Lex>/Hsd17b13<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6N	N	29401633
MGI:7256401	M	MP:0014174	decreased fatty acid beta-oxidation	Hsd17b13<tm1Lex>/Hsd17b13<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6N	N	29401633
MGI:7256401	M	MP:0031116	microvesicular hepatic steatosis	Hsd17b13<tm1Lex>/Hsd17b13<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6N	N	29401633
MGI:7256401	M	MP:0020867	increased lipogenesis	Hsd17b13<tm1Lex>/Hsd17b13<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6N	N	29401633
MGI:7256401	M	MP:0031115	macrovesicular hepatic steatosis	Hsd17b13<tm1Lex>/Hsd17b13<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6N	N	29401633
MGI:7256401	M	MP:0005376	homeostasis/metabolism phenotype	Hsd17b13<tm1Lex>/Hsd17b13<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6N	Y	29401633
MGI:7256401	M	MP:0009355	increased liver triglyceride level	Hsd17b13<tm1Lex>/Hsd17b13<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6N	N	29401633
MGI:7256401	M	MP:0002628	hepatic steatosis	Hsd17b13<tm1Lex>/Hsd17b13<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6N	N	29401633
MGI:7256427	M	MP:0009230	abnormal sperm head morphology	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0005389	reproductive system phenotype	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	Y	29690537
MGI:7256427	M	MP:0009231	detached acrosome	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0031386	elongated manchette	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0031387	abnormal intramanchette transport	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0009234	absent sperm head	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0002687	oligozoospermia	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0002662	abnormal cauda epididymis morphology	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0020869	immotile sperm	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0001925	male infertility	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0009232	abnormal sperm nucleus morphology	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0009239	short sperm flagellum	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0001932	abnormal spermiogenesis	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0009838	abnormal sperm axoneme morphology	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0031356	abnormal outer dense fiber morphology	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0031374	abnormal manchette assembly	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0001155	arrest of spermatogenesis	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0030591	absent sperm fibrous sheath	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	F	MP:0008028	pregnancy-related premature death	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7256427	M	MP:0009242	thin sperm flagellum	Spag17<tm1b(KOMP)Wtsi>/Spag17<tm1b(KOMP)Wtsi>	B6N(Cg)-Spag17<tm1b(KOMP)Wtsi>/J	N	29690537
MGI:7257826	M	MP:0002675	asthenozoospermia	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0031355	abnormal proacrosomal vesicle fusion	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0001935	decreased litter size	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0002687	oligozoospermia	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0009230	abnormal sperm head morphology	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0008892	abnormal sperm flagellum morphology	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0009232	abnormal sperm nucleus morphology	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0014465	abnormal sperm mitochondrial morphology	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0020451	decreased sperm progressive motility	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0030940	impaired autophagy	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0009831	abnormal sperm midpiece morphology	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0001932	abnormal spermiogenesis	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0004542	impaired acrosome reaction	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0009325	necrospermia	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0031374	abnormal manchette assembly	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0008469	abnormal protein level	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0030949	abnormal Golgi vesicle transport	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0009830	abnormal sperm connecting piece morphology	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0001922	reduced male fertility	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0011743	abnormal Golgi apparatus morphology	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0009231	detached acrosome	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0031354	abnormal acrosome assembly	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0002686	globozoospermia	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0008898	abnormal acrosome morphology	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257826	M	MP:0005389	reproductive system phenotype	Pfn3<em1Hsc>/Pfn3<em1Hsc>	involves: C57BL/6 * DBA	Y	34869336
MGI:7257827	M	MP:0009230	abnormal sperm head morphology	Pfn3<em1Hsc>/Pfn3<+>	involves: C57BL/6 * DBA	N	34869336
MGI:7257827	M	MP:0002687	oligozoospermia	Pfn3<em1Hsc>/Pfn3<+>	involves: C57BL/6 * DBA	N	34869336
MGI:7257827	M	MP:0005389	reproductive system phenotype	Pfn3<em1Hsc>/Pfn3<+>	involves: C57BL/6 * DBA	Y	34869336
MGI:7257827	M	MP:0009232	abnormal sperm nucleus morphology	Pfn3<em1Hsc>/Pfn3<+>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0031354	abnormal acrosome assembly	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0001922	reduced male fertility	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0008892	abnormal sperm flagellum morphology	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0002675	asthenozoospermia	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0009831	abnormal sperm midpiece morphology	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0002686	globozoospermia	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0009230	abnormal sperm head morphology	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0005389	reproductive system phenotype	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	Y	34869336
MGI:7257828	M	MP:0001935	decreased litter size	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0031355	abnormal proacrosomal vesicle fusion	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0014465	abnormal sperm mitochondrial morphology	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0011743	abnormal Golgi apparatus morphology	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0031374	abnormal manchette assembly	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0002687	oligozoospermia	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0009830	abnormal sperm connecting piece morphology	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0001932	abnormal spermiogenesis	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0009325	necrospermia	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0030940	impaired autophagy	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0004542	impaired acrosome reaction	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0020451	decreased sperm progressive motility	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0009232	abnormal sperm nucleus morphology	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0008469	abnormal protein level	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0008898	abnormal acrosome morphology	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0030949	abnormal Golgi vesicle transport	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257828	M	MP:0009231	detached acrosome	Pfn3<em2Hsc>/Pfn3<em2Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257829	M	MP:0009232	abnormal sperm nucleus morphology	Pfn3<em2Hsc>/Pfn3<+>	involves: C57BL/6 * DBA	N	34869336
MGI:7257829	M	MP:0005389	reproductive system phenotype	Pfn3<em2Hsc>/Pfn3<+>	involves: C57BL/6 * DBA	Y	34869336
MGI:7257829	M	MP:0002687	oligozoospermia	Pfn3<em2Hsc>/Pfn3<+>	involves: C57BL/6 * DBA	N	34869336
MGI:7257829	M	MP:0009230	abnormal sperm head morphology	Pfn3<em2Hsc>/Pfn3<+>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0009831	abnormal sperm midpiece morphology	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0030949	abnormal Golgi vesicle transport	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0001932	abnormal spermiogenesis	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0008898	abnormal acrosome morphology	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0008892	abnormal sperm flagellum morphology	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0009830	abnormal sperm connecting piece morphology	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0002687	oligozoospermia	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0004542	impaired acrosome reaction	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0031374	abnormal manchette assembly	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0009325	necrospermia	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0030940	impaired autophagy	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0009232	abnormal sperm nucleus morphology	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0005389	reproductive system phenotype	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	Y	34869336
MGI:7257831	M	MP:0009230	abnormal sperm head morphology	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0001922	reduced male fertility	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0002675	asthenozoospermia	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0002686	globozoospermia	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0009231	detached acrosome	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0014465	abnormal sperm mitochondrial morphology	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0031355	abnormal proacrosomal vesicle fusion	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0001935	decreased litter size	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0020451	decreased sperm progressive motility	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0031354	abnormal acrosome assembly	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0008469	abnormal protein level	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257831	M	MP:0011743	abnormal Golgi apparatus morphology	Pfn3<em3Hsc>/Pfn3<em3Hsc>	involves: C57BL/6 * DBA	N	34869336
MGI:7257834	M	MP:0009232	abnormal sperm nucleus morphology	Pfn3<em3Hsc>/Pfn3<+>	involves: C57BL/6 * DBA	N	34869336
MGI:7257834	M	MP:0005389	reproductive system phenotype	Pfn3<em3Hsc>/Pfn3<+>	involves: C57BL/6 * DBA	Y	34869336
MGI:7257834	M	MP:0002687	oligozoospermia	Pfn3<em3Hsc>/Pfn3<+>	involves: C57BL/6 * DBA	N	34869336
MGI:7257834	M	MP:0009230	abnormal sperm head morphology	Pfn3<em3Hsc>/Pfn3<+>	involves: C57BL/6 * DBA	N	34869336
MGI:7258112	M	MP:0009235	small sperm head	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258112	M	MP:0006380	abnormal spermatid morphology	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258112	M	MP:0003674	oxidative stress	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258112	M	MP:0009232	abnormal sperm nucleus morphology	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258112	M	MP:0009232	abnormal sperm nucleus morphology	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258112	M	MP:0020869	immotile sperm	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258112	M	MP:0004543	abnormal sperm physiology	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258112	M	MP:0009231	detached acrosome	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258112	M	MP:0009325	necrospermia	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258112	M	MP:0005389	reproductive system phenotype	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	Y	32727081
MGI:7258112	M	MP:0004543	abnormal sperm physiology	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258112	M	MP:0009230	abnormal sperm head morphology	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258112	M	MP:0001925	male infertility	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258112	M	MP:0009230	abnormal sperm head morphology	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258112	M	MP:0001925	male infertility	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258112	M	MP:0009831	abnormal sperm midpiece morphology	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258112	M	MP:0001932	abnormal spermiogenesis	Prm2<em1Hsc>/Prm2<em1Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258113	M	MP:0005389	reproductive system phenotype	Prm2<em1Hsc>/Prm2<+>	involves: C57BL/6 * DBA/2	Y	27833122
MGI:7258114	M	MP:0005389	reproductive system phenotype	Prm2<em2Hsc>/Prm2<+>	involves: C57BL/6 * DBA/2	Y	27833122
MGI:7258115	M	MP:0004543	abnormal sperm physiology	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258115	M	MP:0009831	abnormal sperm midpiece morphology	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258115	M	MP:0001925	male infertility	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258115	M	MP:0001925	male infertility	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258115	M	MP:0005389	reproductive system phenotype	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	Y	32727081
MGI:7258115	M	MP:0009231	detached acrosome	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258115	M	MP:0006380	abnormal spermatid morphology	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258115	M	MP:0003674	oxidative stress	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258115	M	MP:0009230	abnormal sperm head morphology	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258115	M	MP:0020869	immotile sperm	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258115	M	MP:0009325	necrospermia	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258115	M	MP:0009232	abnormal sperm nucleus morphology	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258115	M	MP:0009232	abnormal sperm nucleus morphology	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258115	M	MP:0001932	abnormal spermiogenesis	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258115	M	MP:0009235	small sperm head	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258115	M	MP:0009230	abnormal sperm head morphology	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	32727081
MGI:7258115	M	MP:0004543	abnormal sperm physiology	Prm2<em2Hsc>/Prm2<em2Hsc>	involves: C57BL/6 * DBA/2	N	27833122
MGI:7258367	M	MP:0005376	homeostasis/metabolism phenotype	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	Y	28823874
MGI:7258367	M	MP:0004930	small epididymis	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0005159	azoospermia	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0009231	detached acrosome	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0031354	abnormal acrosome assembly	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0008279	arrest of spermiogenesis	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0004884	abnormal testis physiology	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0009377	ectopic manchette	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0006380	abnormal spermatid morphology	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0001153	small seminiferous tubules	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0002631	abnormal epididymis morphology	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0002216	abnormal seminiferous tubule morphology	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0008898	abnormal acrosome morphology	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0031374	abnormal manchette assembly	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0004901	decreased male germ cell number	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0001925	male infertility	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0001147	small testis	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7258367	M	MP:0004852	decreased testis weight	Ggnbp2<Gt(IST12476F10)Tigm>/Ggnbp2<Gt(IST12476F10)Tigm>	involves: 129 * C57BL/6N	N	28823874
MGI:7259780	M	MP:0031012	impaired sperm migration in female genital tract	Acrbp<tm1Tba>/Acrbp<tm1Tba>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: 129S2/SvPas * C57BL/6 * DBA/2 * ICR	N	30606959
MGI:7259780	M	MP:0030977	impaired sperm-egg recognition	Acrbp<tm1Tba>/Acrbp<tm1Tba>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: 129S2/SvPas * C57BL/6 * DBA/2 * ICR	N	30606959
MGI:7259780	M	MP:0004542	impaired acrosome reaction	Acrbp<tm1Tba>/Acrbp<tm1Tba>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: 129S2/SvPas * C57BL/6 * DBA/2 * ICR	N	30606959
MGI:7259780	M	MP:0000242	impaired fertilization	Acrbp<tm1Tba>/Acrbp<tm1Tba>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: 129S2/SvPas * C57BL/6 * DBA/2 * ICR	N	30606959
MGI:7259843	F	MP:0004805	absent oocytes	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	18509161
MGI:7259843	F	MP:0001129	impaired ovarian folliculogenesis	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	18509161
MGI:7259843	F	MP:0002777	absent ovarian follicles	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	18509161
MGI:7259843	M	MP:0005389	reproductive system phenotype	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	Y	18509161
MGI:7259843	F	MP:0005431	decreased oocyte number	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	18509161
MGI:7259843	F	MP:0009085	abnormal uterine horn morphology	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	18509161
MGI:7259843	F	MP:0001926	female infertility	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	18509161
MGI:7259843	F	MP:0011121	decreased primordial ovarian follicle number	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	18509161
MGI:7259843	F	MP:0009093	oocyte degeneration	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	18509161
MGI:7259843	F	MP:0011122	absent primordial ovarian follicles	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	18509161
MGI:7259843	F	MP:0004833	ovary atrophy	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	N	18509161
MGI:7259871	F	MP:0030941	enhanced autophagy	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129 * C57BL/6	N	29329412
MGI:7259871	F	MP:0013507	increased ovary apoptosis	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129 * C57BL/6	N	29329412
MGI:7259871	F	MP:0014046	abnormal mitophagy	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129 * C57BL/6	N	29329412
MGI:7259871	F	MP:0010948	abnormal double-strand DNA break repair	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129 * C57BL/6	N	29329412
MGI:7259871	F	MP:0005431	decreased oocyte number	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129 * C57BL/6	N	29329412
MGI:7259871	F	MP:0009093	oocyte degeneration	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129 * C57BL/6	N	29329412
MGI:7259871	F	MP:0031020	premature ovarian failure	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129 * C57BL/6	N	29329412
MGI:7259871	F	MP:0013607	ovary fibrosis	Lhx8<tm1Lmgd>/Lhx8<tm1Lmgd>	involves: 129 * C57BL/6	N	29329412
MGI:7260117	M	MP:0004852	decreased testis weight	Adamts16<em2(IMPC)H>/Adamts16<em2(IMPC)H>	C57BL/6NTac-Adamts16<em2(IMPC)H>	N	31748609
MGI:7260215	M	MP:0001441	increased grooming behavior	Csmd3<em1Yawa>/Csmd3<em1Yawa>	Not Specified	N	35245678
MGI:7261290	M	MP:0001489	decreased startle reflex	Cmya5<tm1Cap>/Cmya5<tm1Cap>	129-Cmya5<tm1Cap>	N	34037836
MGI:7261290	M	MP:0020396	abnormal social recognition	Cmya5<tm1Cap>/Cmya5<tm1Cap>	129-Cmya5<tm1Cap>	N	34037836
MGI:7261290	M	MP:0005386	behavior/neurological phenotype	Cmya5<tm1Cap>/Cmya5<tm1Cap>	129-Cmya5<tm1Cap>	Y	34037836
MGI:7261290	M	MP:0009141	increased prepulse inhibition	Cmya5<tm1Cap>/Cmya5<tm1Cap>	129-Cmya5<tm1Cap>	N	34037836
MGI:7261290	M	MP:0009710	anhedonia	Cmya5<tm1Cap>/Cmya5<tm1Cap>	129-Cmya5<tm1Cap>	N	34037836
MGI:7261290	M	MP:0002797	increased thigmotaxis	Cmya5<tm1Cap>/Cmya5<tm1Cap>	129-Cmya5<tm1Cap>	N	34037836
MGI:7261303	M	MP:0001925	male infertility	Fbxo47<em1Keish>/Fbxo47<em1Keish>	C57BL/6N-Fbxo47<em1Keish>	N	35310947
MGI:7261303	M	MP:0001156	abnormal spermatogenesis	Fbxo47<em1Keish>/Fbxo47<em1Keish>	C57BL/6N-Fbxo47<em1Keish>	N	35310947
MGI:7261303	M	MP:0005159	azoospermia	Fbxo47<em1Keish>/Fbxo47<em1Keish>	C57BL/6N-Fbxo47<em1Keish>	N	35310947
MGI:7261303	F	MP:0005389	reproductive system phenotype	Fbxo47<em1Keish>/Fbxo47<em1Keish>	C57BL/6N-Fbxo47<em1Keish>	Y	35310947
MGI:7261303	M	MP:0009452	abnormal synaptonemal complex	Fbxo47<em1Keish>/Fbxo47<em1Keish>	C57BL/6N-Fbxo47<em1Keish>	N	35310947
MGI:7261303	M	MP:0001147	small testis	Fbxo47<em1Keish>/Fbxo47<em1Keish>	C57BL/6N-Fbxo47<em1Keish>	N	35310947
MGI:7261303	M	MP:0011752	abnormal X-Y chromosome synaptonemal complex assembly during male meiosis	Fbxo47<em1Keish>/Fbxo47<em1Keish>	C57BL/6N-Fbxo47<em1Keish>	N	35310947
MGI:7261303	M	MP:0014052	increased male germ cell apoptosis	Fbxo47<em1Keish>/Fbxo47<em1Keish>	C57BL/6N-Fbxo47<em1Keish>	N	35310947
MGI:7261356	M	MP:0005578	teratozoospermia	Cep128<em1Fzh>/Cep128<em1Fzh>	C57BL/6-Cep128<em1Fzh>	N	35296684
MGI:7261356	M	MP:0001156	abnormal spermatogenesis	Cep128<em1Fzh>/Cep128<em1Fzh>	C57BL/6-Cep128<em1Fzh>	N	35296684
MGI:7261356	M	MP:0009838	abnormal sperm axoneme morphology	Cep128<em1Fzh>/Cep128<em1Fzh>	C57BL/6-Cep128<em1Fzh>	N	35296684
MGI:7261356	M	MP:0008892	abnormal sperm flagellum morphology	Cep128<em1Fzh>/Cep128<em1Fzh>	C57BL/6-Cep128<em1Fzh>	N	35296684
MGI:7261356	M	MP:0020451	decreased sperm progressive motility	Cep128<em1Fzh>/Cep128<em1Fzh>	C57BL/6-Cep128<em1Fzh>	N	35296684
MGI:7261356	M	MP:0002687	oligozoospermia	Cep128<em1Fzh>/Cep128<em1Fzh>	C57BL/6-Cep128<em1Fzh>	N	35296684
MGI:7261356	M	MP:0002675	asthenozoospermia	Cep128<em1Fzh>/Cep128<em1Fzh>	C57BL/6-Cep128<em1Fzh>	N	35296684
MGI:7261356	M	MP:0001925	male infertility	Cep128<em1Fzh>/Cep128<em1Fzh>	C57BL/6-Cep128<em1Fzh>	N	35296684
MGI:7261356	F	MP:0005389	reproductive system phenotype	Cep128<em1Fzh>/Cep128<em1Fzh>	C57BL/6-Cep128<em1Fzh>	Y	35296684
MGI:7261358	M	MP:0001156	abnormal spermatogenesis	Cep128<em2Fzh>/Cep128<em2Fzh>	C57BL/6-Cep128<em2Fzh>	N	35296684
MGI:7261358	M	MP:0005578	teratozoospermia	Cep128<em2Fzh>/Cep128<em2Fzh>	C57BL/6-Cep128<em2Fzh>	N	35296684
MGI:7261358	M	MP:0020451	decreased sperm progressive motility	Cep128<em2Fzh>/Cep128<em2Fzh>	C57BL/6-Cep128<em2Fzh>	N	35296684
MGI:7261358	M	MP:0009838	abnormal sperm axoneme morphology	Cep128<em2Fzh>/Cep128<em2Fzh>	C57BL/6-Cep128<em2Fzh>	N	35296684
MGI:7261358	M	MP:0002675	asthenozoospermia	Cep128<em2Fzh>/Cep128<em2Fzh>	C57BL/6-Cep128<em2Fzh>	N	35296684
MGI:7261358	M	MP:0002687	oligozoospermia	Cep128<em2Fzh>/Cep128<em2Fzh>	C57BL/6-Cep128<em2Fzh>	N	35296684
MGI:7261358	M	MP:0001925	male infertility	Cep128<em2Fzh>/Cep128<em2Fzh>	C57BL/6-Cep128<em2Fzh>	N	35296684
MGI:7261358	M	MP:0008892	abnormal sperm flagellum morphology	Cep128<em2Fzh>/Cep128<em2Fzh>	C57BL/6-Cep128<em2Fzh>	N	35296684
MGI:7261358	F	MP:0005389	reproductive system phenotype	Cep128<em2Fzh>/Cep128<em2Fzh>	C57BL/6-Cep128<em2Fzh>	N	35296684
MGI:7261360	M	MP:0001156	abnormal spermatogenesis	Cep128<em3Fzh>/Cep128<em3Fzh>	C57BL/6-Cep128<em3Fzh>	N	35296684
MGI:7261360	M	MP:0001925	male infertility	Cep128<em3Fzh>/Cep128<em3Fzh>	C57BL/6-Cep128<em3Fzh>	N	35296684
MGI:7261360	M	MP:0009838	abnormal sperm axoneme morphology	Cep128<em3Fzh>/Cep128<em3Fzh>	C57BL/6-Cep128<em3Fzh>	N	35296684
MGI:7261360	M	MP:0005578	teratozoospermia	Cep128<em3Fzh>/Cep128<em3Fzh>	C57BL/6-Cep128<em3Fzh>	N	35296684
MGI:7261360	F	MP:0005389	reproductive system phenotype	Cep128<em3Fzh>/Cep128<em3Fzh>	C57BL/6-Cep128<em3Fzh>	Y	35296684
MGI:7261360	M	MP:0009647	decreased fertilization frequency	Cep128<em3Fzh>/Cep128<em3Fzh>	C57BL/6-Cep128<em3Fzh>	N	35296684
MGI:7261360	M	MP:0002675	asthenozoospermia	Cep128<em3Fzh>/Cep128<em3Fzh>	C57BL/6-Cep128<em3Fzh>	N	35296684
MGI:7261360	M	MP:0002687	oligozoospermia	Cep128<em3Fzh>/Cep128<em3Fzh>	C57BL/6-Cep128<em3Fzh>	N	35296684
MGI:7261360	M	MP:0009243	hairpin sperm flagellum	Cep128<em3Fzh>/Cep128<em3Fzh>	C57BL/6-Cep128<em3Fzh>	N	35296684
MGI:7261372	M	MP:0009831	abnormal sperm midpiece morphology	Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	33476744
MGI:7261372	M	MP:0011630	increased mitochondrial size	Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	33476744
MGI:7261372	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	33476744
MGI:7261372	M	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport	Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	33476744
MGI:7261372	M	MP:0011629	decreased mitochondrial number	Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	33476744
MGI:7261372	M	MP:0011632	dilated mitochondrion	Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	33476744
MGI:7261372	M	MP:0014467	increased sperm mitochondrial size	Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	33476744
MGI:7261372	M	MP:0006035	abnormal mitochondrial morphology	Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * C57BL/6J	N	33476744
MGI:7261374	M	MP:0009647	decreased fertilization frequency	Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	33476744
MGI:7261374	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	33476744
MGI:7261374	M	MP:0011629	decreased mitochondrial number	Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	33476744
MGI:7261374	M	MP:0009237	kinked sperm flagellum	Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	33476744
MGI:7261374	M	MP:0009831	abnormal sperm midpiece morphology	Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	33476744
MGI:7261374	M	MP:0009836	abnormal sperm principal piece morphology	Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	33476744
MGI:7261374	M	MP:0002675	asthenozoospermia	Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	33476744
MGI:7261374	M	MP:0006380	abnormal spermatid morphology	Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	33476744
MGI:7261374	M	MP:0009830	abnormal sperm connecting piece morphology	Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	33476744
MGI:7261374	M	MP:0006035	abnormal mitochondrial morphology	Gt(ROSA)26Sor<tm1.1(CAG-COX8A/Dendra2)Dcc>/Gt(ROSA)26Sor<+>,Mff<Gt(AZ0438)Wtsi>/Mff<Gt(AZ0438)Wtsi>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * C57BL/6J	N	33476744
MGI:7262666	M	MP:0005389	reproductive system phenotype	4930522H14Rik<em1Kher>/4930522H14Rik<em1Kher>	involves: C57BL/6 * DBA/2	Y	35011680
MGI:7262667	M	MP:0005389	reproductive system phenotype	Cct6b<em1Kher>/Cct6b<em1Kher>	involves: C57BL/6 * DBA/2	Y	35011680
MGI:7262695	F	MP:0011129	decreased tertiary ovarian follicle number	Aqp4<tm1Gghu>/Aqp4<tm1Gghu>	involves: 129P2/OlaHsd	N	18976758
MGI:7262695	F	MP:0004856	decreased ovary weight	Aqp4<tm1Gghu>/Aqp4<tm1Gghu>	involves: 129P2/OlaHsd	N	18976758
MGI:7262695	F	MP:0001129	impaired ovarian folliculogenesis	Aqp4<tm1Gghu>/Aqp4<tm1Gghu>	involves: 129P2/OlaHsd	N	18976758
MGI:7262695	F	MP:0002680	decreased corpora lutea number	Aqp4<tm1Gghu>/Aqp4<tm1Gghu>	involves: 129P2/OlaHsd	N	18976758
MGI:7262695	F	MP:0001935	decreased litter size	Aqp4<tm1Gghu>/Aqp4<tm1Gghu>	involves: 129P2/OlaHsd	N	18976758
MGI:7262695	F	MP:0002637	small uterus	Aqp4<tm1Gghu>/Aqp4<tm1Gghu>	involves: 129P2/OlaHsd	N	18976758
MGI:7262695	F	MP:0031420	decreased superovulation rate	Aqp4<tm1Gghu>/Aqp4<tm1Gghu>	involves: 129P2/OlaHsd	N	18976758
MGI:7262695	F	MP:0009671	abnormal uterus physiology	Aqp4<tm1Gghu>/Aqp4<tm1Gghu>	involves: 129P2/OlaHsd	N	18976758
MGI:7262695	F	MP:0004905	decreased uterus weight	Aqp4<tm1Gghu>/Aqp4<tm1Gghu>	involves: 129P2/OlaHsd	N	18976758
MGI:7262695	F	MP:0008258	thin endometrium	Aqp4<tm1Gghu>/Aqp4<tm1Gghu>	involves: 129P2/OlaHsd	N	18976758
MGI:7262695	F	MP:0001923	reduced female fertility	Aqp4<tm1Gghu>/Aqp4<tm1Gghu>	involves: 129P2/OlaHsd	N	18976758
MGI:7262850	F	MP:0031424	enhanced female fertility	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: C57BL/6	N	21117174
MGI:7262850	F	MP:0001934	increased litter size	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: C57BL/6	N	21117174
MGI:7262850	F	MP:0001130	abnormal ovarian folliculogenesis	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: C57BL/6	N	21117174
MGI:7262850	F	MP:0001784	abnormal fluid regulation	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: C57BL/6	N	21117174
MGI:7262850	F	MP:0001928	abnormal ovulation	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: C57BL/6	N	21117174
MGI:7262850	F	MP:0031421	increased superovulation rate	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: C57BL/6	N	21117174
MGI:7262850	M	MP:0005389	reproductive system phenotype	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: C57BL/6	Y	21117174
MGI:7262850	F	MP:0031016	decreased granulosa cell apoptosis	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: C57BL/6	N	21117174
MGI:7262850	F	MP:0002681	increased corpora lutea number	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: C57BL/6	N	21117174
MGI:7262850	F	MP:0031411	increased ovulation rate	Aqp8<tm1Ask>/Aqp8<tm1Ask>	involves: C57BL/6	N	21117174
MGI:7262878	F	MP:0001127	small ovary	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0009093	oocyte degeneration	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0011121	decreased primordial ovarian follicle number	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0004833	ovary atrophy	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0031381	decreased secondary ovarian follicle number	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0005181	decreased circulating estradiol level	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0001129	impaired ovarian folliculogenesis	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0001935	decreased litter size	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0001923	reduced female fertility	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0031420	decreased superovulation rate	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0002680	decreased corpora lutea number	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0031018	decreased granulosa cell proliferation	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0011129	decreased tertiary ovarian follicle number	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0013508	increased granulosa cell apoptosis	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0011125	decreased primary ovarian follicle number	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0001750	increased circulating follicle stimulating hormone level	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0031020	premature ovarian failure	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0004856	decreased ovary weight	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7262878	F	MP:0031239	increased atretic ovarian follicle number	Cpeb3<em1Gaoxu>/Cpeb3<em1Gaoxu>	C57BL/6J-Cpeb3<em1Gaoxu>	N	34930897
MGI:7264294	F	MP:0001926	female infertility	Gata2<tm1Sac>/Gata2<tm1Sac>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27783953
MGI:7264294	F	MP:0009671	abnormal uterus physiology	Gata2<tm1Sac>/Gata2<tm1Sac>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27783953
MGI:7264294	F	MP:0004896	abnormal endometrium morphology	Gata2<tm1Sac>/Gata2<tm1Sac>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27783953
MGI:7264294	F	MP:0003845	abnormal decidualization	Gata2<tm1Sac>/Gata2<tm1Sac>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27783953
MGI:7264294	F	MP:0001728	failure of embryo implantation	Gata2<tm1Sac>/Gata2<tm1Sac>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129S1/Sv * 129X1/SvJ	N	27783953
MGI:7265077	M	MP:0002557	abnormal social/conspecific interaction behavior	Myt1l<em1Jdd>/Myt1l<+>	C57BL/6-Myt1l<em1Jdd>/J	N	34614421
MGI:7265077	F	MP:0002574	increased vertical activity	Myt1l<em1Jdd>/Myt1l<+>	C57BL/6-Myt1l<em1Jdd>/J	N	34614421
MGI:7266261	M	MP:0002175	decreased brain weight	Mecp2<tm1Nlnd>/Y	involves: 129 * C57BL/6J	N	30402709
MGI:7266261	M	MP:0004924	abnormal behavior	Mecp2<tm1Nlnd>/Y	involves: 129 * C57BL/6J	N	30402709
MGI:7266261	M	MP:0000745	tremors	Mecp2<tm1Nlnd>/Y	involves: 129 * C57BL/6J	N	30402709
MGI:7266261	M	MP:0001262	decreased body weight	Mecp2<tm1Nlnd>/Y	involves: 129 * C57BL/6J	N	30402709
MGI:7266261	M	MP:0002083	premature death	Mecp2<tm1Nlnd>/Y	involves: 129 * C57BL/6J	N	30402709
MGI:7266261	M	MP:0001513	limb grasping	Mecp2<tm1Nlnd>/Y	involves: 129 * C57BL/6J	N	30402709
MGI:7266266	M	MP:0010053	decreased grip strength	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0001260	increased body weight	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0001407	short stride length	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0000745	tremors	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0008489	slow postnatal weight gain	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0001513	limb grasping	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0004924	abnormal behavior	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0003646	increased muscle fatigability	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0001405	impaired coordination	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0002175	decreased brain weight	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0004811	abnormal neuron physiology	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0008428	abnormal spatial working memory	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0009456	impaired cued conditioning behavior	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0001402	decreased locomotor activity	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266266	M	MP:0002083	premature death	Mecp2<tm1Nlnd>/Y	involves: 129 * CD-1	N	30402709
MGI:7266283	F	MP:0010768	mortality/aging	Mecp2<tm1Nlnd>/Mecp2<+>	involves: 129 * CD-1	Y	30402709
MGI:7266283	F	MP:0000745	tremors	Mecp2<tm1Nlnd>/Mecp2<+>	involves: 129 * CD-1	N	30402709
MGI:7266283	F	MP:0001513	limb grasping	Mecp2<tm1Nlnd>/Mecp2<+>	involves: 129 * CD-1	N	30402709
MGI:7266283	F	MP:0004924	abnormal behavior	Mecp2<tm1Nlnd>/Mecp2<+>	involves: 129 * CD-1	N	30402709
MGI:7266283	F	MP:0001261	obese	Mecp2<tm1Nlnd>/Mecp2<+>	involves: 129 * CD-1	N	30402709
MGI:7266284	M	MP:0001405	impaired coordination	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * CD-1	N	30402709
MGI:7266284	M	MP:0001407	short stride length	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * CD-1	N	30402709
MGI:7266284	M	MP:0008428	abnormal spatial working memory	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * CD-1	N	30402709
MGI:7266284	M	MP:0003646	increased muscle fatigability	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * CD-1	N	30402709
MGI:7266284	M	MP:0010053	decreased grip strength	Mecp2<tm1.1Bird>/Y	involves: 129P2/OlaHsd * CD-1	N	30402709
MGI:7266812	M	MP:0008892	abnormal sperm flagellum morphology	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0001147	small testis	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0010948	abnormal double-strand DNA break repair	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0001154	seminiferous tubule degeneration	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0001922	reduced male fertility	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0001155	arrest of spermatogenesis	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0003702	abnormal chromosome morphology	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0009230	abnormal sperm head morphology	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0009234	absent sperm head	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0002687	oligozoospermia	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0001153	small seminiferous tubules	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0004901	decreased male germ cell number	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0004852	decreased testis weight	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0014052	increased male germ cell apoptosis	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0009451	abnormal chromosomal synapsis	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0004023	abnormal chromosome number	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0005578	teratozoospermia	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266812	M	MP:0008261	arrest of male meiosis	Tardbp<tm1.1Pcw>/Tardbp<tm1.1Pcw>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ * SJL	N	34599968
MGI:7266825	F	MP:0001131	abnormal ovarian follicle morphology	Atr<tm1Ofc>/Atr<tm1Ofc>	involves: 129 * C57BL/6	N	31489491
MGI:7266825	F	MP:0011125	decreased primary ovarian follicle number	Atr<tm1Ofc>/Atr<tm1Ofc>	involves: 129 * C57BL/6	N	31489491
MGI:7266825	F	MP:0013508	increased granulosa cell apoptosis	Atr<tm1Ofc>/Atr<tm1Ofc>	involves: 129 * C57BL/6	N	31489491
MGI:7266825	F	MP:0011120	increased primordial ovarian follicle number	Atr<tm1Ofc>/Atr<tm1Ofc>	involves: 129 * C57BL/6	N	31489491
MGI:7266825	F	MP:0031381	decreased secondary ovarian follicle number	Atr<tm1Ofc>/Atr<tm1Ofc>	involves: 129 * C57BL/6	N	31489491
MGI:7266825	F	MP:0031019	increased granulosa cell proliferation	Atr<tm1Ofc>/Atr<tm1Ofc>	involves: 129 * C57BL/6	N	31489491
MGI:7266825	F	MP:0005168	abnormal female meiosis	Atr<tm1Ofc>/Atr<tm1Ofc>	involves: 129 * C57BL/6	N	31489491
MGI:7266825	F	MP:0031018	decreased granulosa cell proliferation	Atr<tm1Ofc>/Atr<tm1Ofc>	involves: 129 * C57BL/6	N	31489491
MGI:7266825	F	MP:0001129	impaired ovarian folliculogenesis	Atr<tm1Ofc>/Atr<tm1Ofc>	involves: 129 * C57BL/6	N	31489491
MGI:7266959	F	MP:0010024	increased total body fat amount	4930447C04Rik<em1(IMPC)Bay>/4930447C04Rik<em1(IMPC)Bay>	C57BL/6N-4930447C04Rik<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7266959	M	MP:0001925	male infertility	4930447C04Rik<em1(IMPC)Bay>/4930447C04Rik<em1(IMPC)Bay>	C57BL/6N-4930447C04Rik<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7266959	F	MP:0001926	female infertility	4930447C04Rik<em1(IMPC)Bay>/4930447C04Rik<em1(IMPC)Bay>	C57BL/6N-4930447C04Rik<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7266959	F	MP:0000063	decreased bone mineral density	4930447C04Rik<em1(IMPC)Bay>/4930447C04Rik<em1(IMPC)Bay>	C57BL/6N-4930447C04Rik<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7266959	F	MP:0010124	decreased bone mineral content	4930447C04Rik<em1(IMPC)Bay>/4930447C04Rik<em1(IMPC)Bay>	C57BL/6N-4930447C04Rik<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7266959	F	MP:0003961	decreased lean body mass	4930447C04Rik<em1(IMPC)Bay>/4930447C04Rik<em1(IMPC)Bay>	C57BL/6N-4930447C04Rik<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7266960	F	MP:0001417	decreased exploration in new environment	Actl6a<em1(IMPC)J>/Actl6a<+>	C57BL/6NJ-Actl6a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266961	F	MP:0001402	decreased locomotor activity	Actr3b<em1(IMPC)J>/Actr3b<em1(IMPC)J>	C57BL/6NJ-Actr3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266961	F	MP:0020870	decreased thigmotaxis	Actr3b<em1(IMPC)J>/Actr3b<em1(IMPC)J>	C57BL/6NJ-Actr3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266962	F	MP:0005559	increased circulating glucose level	Acyp1<em1(IMPC)J>/Acyp1<em1(IMPC)J>	C57BL/6NJ-Acyp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266962	M	MP:0003960	increased lean body mass	Acyp1<em1(IMPC)J>/Acyp1<em1(IMPC)J>	C57BL/6NJ-Acyp1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266963	M	MP:0003131	increased erythrocyte cell number	Aftph<em1(IMPC)J>/Aftph<+>	C57BL/6NJ-Aftph<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266963	M	MP:0000198	decreased circulating phosphate level	Aftph<em1(IMPC)J>/Aftph<+>	C57BL/6NJ-Aftph<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266965	M	MP:0002875	decreased erythrocyte cell number	Anapc7<em1(IMPC)J>/Anapc7<em1(IMPC)J>	C57BL/6NJ-Anapc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266965	F	MP:0001926	female infertility	Anapc7<em1(IMPC)J>/Anapc7<em1(IMPC)J>	C57BL/6NJ-Anapc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266965	F	MP:0002591	decreased mean corpuscular volume	Anapc7<em1(IMPC)J>/Anapc7<em1(IMPC)J>	C57BL/6NJ-Anapc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266965	F	MP:0003795	abnormal bone structure	Anapc7<em1(IMPC)J>/Anapc7<em1(IMPC)J>	C57BL/6NJ-Anapc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266965	F	MP:0005333	decreased heart rate	Anapc7<em1(IMPC)J>/Anapc7<em1(IMPC)J>	C57BL/6NJ-Anapc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266965	F	MP:0010124	decreased bone mineral content	Anapc7<em1(IMPC)J>/Anapc7<em1(IMPC)J>	C57BL/6NJ-Anapc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266965	M	MP:0000208	decreased hematocrit	Anapc7<em1(IMPC)J>/Anapc7<em1(IMPC)J>	C57BL/6NJ-Anapc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266965	F	MP:0010024	increased total body fat amount	Anapc7<em1(IMPC)J>/Anapc7<em1(IMPC)J>	C57BL/6NJ-Anapc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266965	F	MP:0010506	prolonged RR interval	Anapc7<em1(IMPC)J>/Anapc7<em1(IMPC)J>	C57BL/6NJ-Anapc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266967	F	MP:0002591	decreased mean corpuscular volume	Ankrd13c<em1(IMPC)Tcp>/Ankrd13c<em1(IMPC)Tcp>	C57BL/6N-Ankrd13c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7266967	F	MP:0005562	decreased mean corpuscular hemoglobin	Ankrd13c<em1(IMPC)Tcp>/Ankrd13c<em1(IMPC)Tcp>	C57BL/6N-Ankrd13c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7266967	F	MP:0001944	abnormal pancreas morphology	Ankrd13c<em1(IMPC)Tcp>/Ankrd13c<em1(IMPC)Tcp>	C57BL/6N-Ankrd13c<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7266968	M	MP:0003233	prolonged QT interval	Ap1s3<em1(IMPC)Bay>/Ap1s3<em1(IMPC)Bay>	C57BL/6N-Ap1s3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7266969	F	MP:0001392	abnormal locomotor behavior	Arglu1<em1(IMPC)J>/Arglu1<+>	C57BL/6NJ-Arglu1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266973	M	MP:0011874	enlarged urinary bladder	Arrdc4<em1(IMPC)Tcp>/Arrdc4<em1(IMPC)Tcp>	C57BL/6N-Arrdc4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7266973	M	MP:0000702	enlarged lymph nodes	Arrdc4<em1(IMPC)Tcp>/Arrdc4<em1(IMPC)Tcp>	C57BL/6N-Arrdc4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7266973	M	MP:0010067	increased red blood cell distribution width	Arrdc4<em1(IMPC)Tcp>/Arrdc4<em1(IMPC)Tcp>	C57BL/6N-Arrdc4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7266973	M	MP:0000220	increased monocyte cell number	Arrdc4<em1(IMPC)Tcp>/Arrdc4<em1(IMPC)Tcp>	C57BL/6N-Arrdc4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7266974	F	MP:0001284	absent vibrissae	Ascl4<em1(IMPC)J>/Ascl4<em1(IMPC)J>	C57BL/6NJ-Ascl4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266974	F	MP:0000218	increased leukocyte cell number	Ascl4<em1(IMPC)J>/Ascl4<em1(IMPC)J>	C57BL/6NJ-Ascl4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266976	F	MP:0010123	increased bone mineral content	Atxn7<em1(IMPC)Bay>/Atxn7<em1(IMPC)Bay>	C57BL/6N-Atxn7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7266977	F	MP:0002590	increased mean corpuscular volume	Bicra<em1(IMPC)J>/Bicra<+>	C57BL/6NJ-Bicra<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266981	M	MP:0003960	increased lean body mass	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<+>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266981	M	MP:0001146	abnormal testis morphology	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<+>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266981	F	MP:0002699	abnormal vitreous body morphology	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<+>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266981	M	MP:0010025	decreased total body fat amount	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<+>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266981	M	MP:0001148	enlarged testis	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<+>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266981	F	MP:0001304	cataract	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<+>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266981	M	MP:0002060	abnormal skin morphology	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<+>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266981	F	MP:0002989	small kidney	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<+>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266981	M	MP:0004952	increased spleen weight	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<+>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266981	M	MP:0003068	enlarged kidney	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<+>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266982	M	MP:0000745	tremors	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<em1(IMPC)Mbp>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266982	M	MP:0001406	abnormal gait	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<em1(IMPC)Mbp>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266982	M	MP:0002059	abnormal seminal vesicle morphology	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<em1(IMPC)Mbp>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266982	M	MP:0001157	small seminal vesicle	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<em1(IMPC)Mbp>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266982	F	MP:0001926	female infertility	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<em1(IMPC)Mbp>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266982	M	MP:0000266	abnormal heart morphology	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<em1(IMPC)Mbp>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266982	M	MP:0000689	abnormal spleen morphology	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<em1(IMPC)Mbp>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266982	M	MP:0002188	small heart	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<em1(IMPC)Mbp>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266982	M	MP:0001711	abnormal placenta morphology	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<em1(IMPC)Mbp>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266982	M	MP:0000692	small spleen	Cacna2d2<em1(IMPC)Mbp>/Cacna2d2<em1(IMPC)Mbp>	C57BL/6N-Cacna2d2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266986	F	MP:0002968	increased circulating alkaline phosphatase level	Cdkn2aip<em1(IMPC)J>/Cdkn2aip<em1(IMPC)J>	C57BL/6NJ-Cdkn2aip<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266986	F	MP:0005565	increased blood urea nitrogen level	Cdkn2aip<em1(IMPC)J>/Cdkn2aip<em1(IMPC)J>	C57BL/6NJ-Cdkn2aip<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266987	F	MP:0000689	abnormal spleen morphology	Celsr1<em1(IMPC)Mbp>/Celsr1<+>	C57BL/6N-Celsr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266987	F	MP:0002060	abnormal skin morphology	Celsr1<em1(IMPC)Mbp>/Celsr1<+>	C57BL/6N-Celsr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266987	M	MP:0001146	abnormal testis morphology	Celsr1<em1(IMPC)Mbp>/Celsr1<+>	C57BL/6N-Celsr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266987	F	MP:0002152	abnormal brain morphology	Celsr1<em1(IMPC)Mbp>/Celsr1<+>	C57BL/6N-Celsr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266987	M	MP:0001148	enlarged testis	Celsr1<em1(IMPC)Mbp>/Celsr1<+>	C57BL/6N-Celsr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266987	M	MP:0002699	abnormal vitreous body morphology	Celsr1<em1(IMPC)Mbp>/Celsr1<+>	C57BL/6N-Celsr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266987	F	MP:0005238	increased brain size	Celsr1<em1(IMPC)Mbp>/Celsr1<+>	C57BL/6N-Celsr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266987	M	MP:0001304	cataract	Celsr1<em1(IMPC)Mbp>/Celsr1<+>	C57BL/6N-Celsr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266987	F	MP:0000691	enlarged spleen	Celsr1<em1(IMPC)Mbp>/Celsr1<+>	C57BL/6N-Celsr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266988	M	MP:0001417	decreased exploration in new environment	Cerkl<tm1b(KOMP)Wtsi>/Cerkl<tm1b(KOMP)Wtsi>	C57BL/6N-Cerkl<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:7266989	F	MP:0002989	small kidney	Chrnd<em1(IMPC)Mbp>/Chrnd<+>	C57BL/6N-Chrnd<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266989	F	MP:0002060	abnormal skin morphology	Chrnd<em1(IMPC)Mbp>/Chrnd<+>	C57BL/6N-Chrnd<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266989	F	MP:0002699	abnormal vitreous body morphology	Chrnd<em1(IMPC)Mbp>/Chrnd<+>	C57BL/6N-Chrnd<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266989	F	MP:0002135	abnormal kidney morphology	Chrnd<em1(IMPC)Mbp>/Chrnd<+>	C57BL/6N-Chrnd<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266990	F	MP:0001297	microphthalmia	Chrnd<em1(IMPC)Mbp>/Chrnd<em1(IMPC)Mbp>	C57BL/6N-Chrnd<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7266992	M	MP:0005333	decreased heart rate	Cpa5<em1(IMPC)J>/Cpa5<em1(IMPC)J>	C57BL/6NJ-Cpa5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266992	M	MP:0010506	prolonged RR interval	Cpa5<em1(IMPC)J>/Cpa5<em1(IMPC)J>	C57BL/6NJ-Cpa5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266992	M	MP:0005635	decreased circulating bilirubin level	Cpa5<em1(IMPC)J>/Cpa5<em1(IMPC)J>	C57BL/6NJ-Cpa5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7266994	F	MP:0002060	abnormal skin morphology	Cpq<em1(IMPC)Tcp>/Cpq<em1(IMPC)Tcp>	C57BL/6N-Cpq<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7266994	M	MP:0000702	enlarged lymph nodes	Cpq<em1(IMPC)Tcp>/Cpq<em1(IMPC)Tcp>	C57BL/6N-Cpq<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7266994	M	MP:0005562	decreased mean corpuscular hemoglobin	Cpq<em1(IMPC)Tcp>/Cpq<em1(IMPC)Tcp>	C57BL/6N-Cpq<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7266996	F	MP:0020421	increased freezing behavior	Dapk3<tm1b(EUCOMM)Hmgu>/Dapk3<+>	C57BL/6N-Dapk3<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7266996	M	MP:0001399	hyperactivity	Dapk3<tm1b(EUCOMM)Hmgu>/Dapk3<+>	C57BL/6N-Dapk3<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7267000	M	MP:0002834	decreased heart weight	Dytn<em1(IMPC)J>/Dytn<em1(IMPC)J>	C57BL/6NJ-Dytn<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267000	F	MP:0001415	increased exploration in new environment	Dytn<em1(IMPC)J>/Dytn<em1(IMPC)J>	C57BL/6NJ-Dytn<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267000	M	MP:0010124	decreased bone mineral content	Dytn<em1(IMPC)J>/Dytn<em1(IMPC)J>	C57BL/6NJ-Dytn<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267001	F	MP:0000062	increased bone mineral density	Ube2q2l<em1(IMPC)J>/Ube2q2l<em1(IMPC)J>	C57BL/6NJ-Ube2q2l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267002	F	MP:0001257	increased body length	Ebf4<em1(IMPC)Bay>/Ebf4<em1(IMPC)Bay>	C57BL/6N-Ebf4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267004	F	MP:0010052	increased grip strength	Eid2b<em1(IMPC)J>/Eid2b<+>	C57BL/6NJ-Eid2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267004	F	MP:0000195	decreased circulating calcium level	Eid2b<em1(IMPC)J>/Eid2b<+>	C57BL/6NJ-Eid2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267004	F	MP:0005559	increased circulating glucose level	Eid2b<em1(IMPC)J>/Eid2b<+>	C57BL/6NJ-Eid2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267004	M	MP:0000062	increased bone mineral density	Eid2b<em1(IMPC)J>/Eid2b<+>	C57BL/6NJ-Eid2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267004	F	MP:0002591	decreased mean corpuscular volume	Eid2b<em1(IMPC)J>/Eid2b<+>	C57BL/6NJ-Eid2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267006	M	MP:0001417	decreased exploration in new environment	Elovl4<tm2b(EUCOMM)Hmgu>/Elovl4<+>	C57BL/6N-Elovl4<tm2b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:7267007	M	MP:0003960	increased lean body mass	Ensa<em1(IMPC)J>/Ensa<em1(IMPC)J>	C57BL/6NJ-Ensa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267007	M	MP:0000195	decreased circulating calcium level	Ensa<em1(IMPC)J>/Ensa<em1(IMPC)J>	C57BL/6NJ-Ensa<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267010	M	MP:0001488	increased startle reflex	Exoc3l<em1(IMPC)J>/Exoc3l<em1(IMPC)J>	C57BL/6NJ-Exoc3l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267011	M	MP:0009142	decreased prepulse inhibition	Fam117a<em1(IMPC)Bay>/Fam117a<em1(IMPC)Bay>	C57BL/6N-Fam117a<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267012	M	MP:0000759	abnormal skeletal muscle morphology	Fam161b<em1(IMPC)Ccpcz>/Fam161b<em1(IMPC)Ccpcz>	C57BL/6N-Fam161b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267012	M	MP:0002339	abnormal lymph node morphology	Fam161b<em1(IMPC)Ccpcz>/Fam161b<em1(IMPC)Ccpcz>	C57BL/6N-Fam161b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267012	F	MP:0000709	enlarged thymus	Fam161b<em1(IMPC)Ccpcz>/Fam161b<em1(IMPC)Ccpcz>	C57BL/6N-Fam161b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267012	M	MP:0000274	enlarged heart	Fam161b<em1(IMPC)Ccpcz>/Fam161b<em1(IMPC)Ccpcz>	C57BL/6N-Fam161b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267012	M	MP:0000702	enlarged lymph nodes	Fam161b<em1(IMPC)Ccpcz>/Fam161b<em1(IMPC)Ccpcz>	C57BL/6N-Fam161b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267012	M	MP:0000266	abnormal heart morphology	Fam161b<em1(IMPC)Ccpcz>/Fam161b<em1(IMPC)Ccpcz>	C57BL/6N-Fam161b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267012	F	MP:0000703	abnormal thymus morphology	Fam161b<em1(IMPC)Ccpcz>/Fam161b<em1(IMPC)Ccpcz>	C57BL/6N-Fam161b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267014	F	MP:0000709	enlarged thymus	Fam81a<em1(IMPC)Ccpcz>/Fam81a<em1(IMPC)Ccpcz>	C57BL/6N-Fam81a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267014	F	MP:0000703	abnormal thymus morphology	Fam81a<em1(IMPC)Ccpcz>/Fam81a<em1(IMPC)Ccpcz>	C57BL/6N-Fam81a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267014	F	MP:0000691	enlarged spleen	Fam81a<em1(IMPC)Ccpcz>/Fam81a<em1(IMPC)Ccpcz>	C57BL/6N-Fam81a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267014	M	MP:0001489	decreased startle reflex	Fam81a<em1(IMPC)Ccpcz>/Fam81a<em1(IMPC)Ccpcz>	C57BL/6N-Fam81a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267014	F	MP:0000689	abnormal spleen morphology	Fam81a<em1(IMPC)Ccpcz>/Fam81a<em1(IMPC)Ccpcz>	C57BL/6N-Fam81a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267015	F	MP:0010097	abnormal retina blood vessel morphology	Frmd4a<em1(IMPC)J>/Frmd4a<+>	C57BL/6NJ-Frmd4a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267015	M	MP:0000195	decreased circulating calcium level	Frmd4a<em1(IMPC)J>/Frmd4a<+>	C57BL/6NJ-Frmd4a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267016	M	MP:0001314	cornea opacity	Galnt9<em1(IMPC)H>/Galnt9<em1(IMPC)H>	C57BL/6N-Galnt9<em1(IMPC)H>/H	N	MGI:5576271
MGI:7267017	M	MP:0005293	impaired glucose tolerance	Brcc3dc<em1(IMPC)J>/Brcc3dc<em1(IMPC)J>	C57BL/6NJ-Brcc3dc<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267021	M	MP:0001304	cataract	Il36rn<em1(IMPC)Mbp>/Il36rn<em1(IMPC)Mbp>	C57BL/6N-Il36rn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267021	F	MP:0002060	abnormal skin morphology	Il36rn<em1(IMPC)Mbp>/Il36rn<em1(IMPC)Mbp>	C57BL/6N-Il36rn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267021	M	MP:0002135	abnormal kidney morphology	Il36rn<em1(IMPC)Mbp>/Il36rn<em1(IMPC)Mbp>	C57BL/6N-Il36rn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267021	M	MP:0002989	small kidney	Il36rn<em1(IMPC)Mbp>/Il36rn<em1(IMPC)Mbp>	C57BL/6N-Il36rn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267022	F	MP:0000198	decreased circulating phosphate level	Insyn2b<em1(IMPC)J>/Insyn2b<em1(IMPC)J>	C57BL/6NJ-Insyn2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267022	M	MP:0000218	increased leukocyte cell number	Insyn2b<em1(IMPC)J>/Insyn2b<em1(IMPC)J>	C57BL/6NJ-Insyn2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267022	M	MP:0002941	increased circulating alanine transaminase level	Insyn2b<em1(IMPC)J>/Insyn2b<em1(IMPC)J>	C57BL/6NJ-Insyn2b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267024	M	MP:0005599	increased cardiac muscle contractility	Izumo2<em1(IMPC)Bay>/Izumo2<em1(IMPC)Bay>	C57BL/6N-Izumo2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267024	M	MP:0002626	increased heart rate	Izumo2<em1(IMPC)Bay>/Izumo2<em1(IMPC)Bay>	C57BL/6N-Izumo2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267025	F	MP:0001364	decreased anxiety-related response	Jakmip2<em1(IMPC)J>/Jakmip2<em1(IMPC)J>	C57BL/6NJ-Jakmip2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267025	M	MP:0001488	increased startle reflex	Jakmip2<em1(IMPC)J>/Jakmip2<em1(IMPC)J>	C57BL/6NJ-Jakmip2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267025	M	MP:0005559	increased circulating glucose level	Jakmip2<em1(IMPC)J>/Jakmip2<em1(IMPC)J>	C57BL/6NJ-Jakmip2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267025	M	MP:0005635	decreased circulating bilirubin level	Jakmip2<em1(IMPC)J>/Jakmip2<em1(IMPC)J>	C57BL/6NJ-Jakmip2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267026	F	MP:0010506	prolonged RR interval	Kcna7<em1(IMPC)J>/Kcna7<em1(IMPC)J>	C57BL/6NJ-Kcna7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267026	F	MP:0005333	decreased heart rate	Kcna7<em1(IMPC)J>/Kcna7<em1(IMPC)J>	C57BL/6NJ-Kcna7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267027	F	MP:0005559	increased circulating glucose level	Klhdc10<em1(IMPC)J>/Klhdc10<em1(IMPC)J>	C57BL/6NJ-Klhdc10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267029	F	MP:0003917	increased kidney weight	Krtap9-5<em1(IMPC)Ccpcz>/Krtap9-5<em1(IMPC)Ccpcz>	C57BL/6N-Krtap9-5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267029	F	MP:0002135	abnormal kidney morphology	Krtap9-5<em1(IMPC)Ccpcz>/Krtap9-5<em1(IMPC)Ccpcz>	C57BL/6N-Krtap9-5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267029	M	MP:0013129	abnormal tooth color	Krtap9-5<em1(IMPC)Ccpcz>/Krtap9-5<em1(IMPC)Ccpcz>	C57BL/6N-Krtap9-5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267029	F	MP:0000689	abnormal spleen morphology	Krtap9-5<em1(IMPC)Ccpcz>/Krtap9-5<em1(IMPC)Ccpcz>	C57BL/6N-Krtap9-5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267029	M	MP:0002100	abnormal tooth morphology	Krtap9-5<em1(IMPC)Ccpcz>/Krtap9-5<em1(IMPC)Ccpcz>	C57BL/6N-Krtap9-5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267030	M	MP:0010052	increased grip strength	Ky<em1(IMPC)J>/Ky<em1(IMPC)J>	C57BL/6NJ-Ky<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267030	M	MP:0001523	impaired righting response	Ky<em1(IMPC)J>/Ky<em1(IMPC)J>	C57BL/6NJ-Ky<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267031	M	MP:0000157	abnormal sternum morphology	Lage3<em1(IMPC)Tcp>/Y	C57BL/6N-Lage3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7267032	M	MP:0000063	decreased bone mineral density	Lancl3<em1(IMPC)H>/Y	C57BL/6N-Lancl3<em1(IMPC)H>/H	N	MGI:5576271
MGI:7267032	M	MP:0002965	increased circulating serum albumin level	Lancl3<em1(IMPC)H>/Y	C57BL/6N-Lancl3<em1(IMPC)H>/H	N	MGI:5576271
MGI:7267033	F	MP:0005333	decreased heart rate	Lcorl<em1(IMPC)J>/Lcorl<em1(IMPC)J>	C57BL/6NJ-Lcorl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267033	F	MP:0001415	increased exploration in new environment	Lcorl<em1(IMPC)J>/Lcorl<em1(IMPC)J>	C57BL/6NJ-Lcorl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267033	F	MP:0005655	increased aggression	Lcorl<em1(IMPC)J>/Lcorl<em1(IMPC)J>	C57BL/6NJ-Lcorl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267033	F	MP:0001399	hyperactivity	Lcorl<em1(IMPC)J>/Lcorl<em1(IMPC)J>	C57BL/6NJ-Lcorl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267034	F	MP:0008810	increased circulating iron level	Lrp1b<em1(IMPC)Hmgu>/Lrp1b<+>	C57BL/6N-Lrp1b<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7267034	F	MP:0011897	decreased circulating unsaturated transferrin level	Lrp1b<em1(IMPC)Hmgu>/Lrp1b<+>	C57BL/6N-Lrp1b<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7267036	F	MP:0000703	abnormal thymus morphology	Lrrc17<em1(IMPC)Ccpcz>/Lrrc17<em1(IMPC)Ccpcz>	C57BL/6N-Lrrc17<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267036	F	MP:0005084	abnormal gallbladder morphology	Lrrc17<em1(IMPC)Ccpcz>/Lrrc17<em1(IMPC)Ccpcz>	C57BL/6N-Lrrc17<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267036	F	MP:0020421	increased freezing behavior	Lrrc17<em1(IMPC)Ccpcz>/Lrrc17<em1(IMPC)Ccpcz>	C57BL/6N-Lrrc17<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267036	M	MP:0002631	abnormal epididymis morphology	Lrrc17<em1(IMPC)Ccpcz>/Lrrc17<em1(IMPC)Ccpcz>	C57BL/6N-Lrrc17<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267036	M	MP:0004931	enlarged epididymis	Lrrc17<em1(IMPC)Ccpcz>/Lrrc17<em1(IMPC)Ccpcz>	C57BL/6N-Lrrc17<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267036	F	MP:0000709	enlarged thymus	Lrrc17<em1(IMPC)Ccpcz>/Lrrc17<em1(IMPC)Ccpcz>	C57BL/6N-Lrrc17<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267036	F	MP:0009342	enlarged gallbladder	Lrrc17<em1(IMPC)Ccpcz>/Lrrc17<em1(IMPC)Ccpcz>	C57BL/6N-Lrrc17<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267036	F	MP:0000691	enlarged spleen	Lrrc17<em1(IMPC)Ccpcz>/Lrrc17<em1(IMPC)Ccpcz>	C57BL/6N-Lrrc17<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267036	F	MP:0002797	increased thigmotaxis	Lrrc17<em1(IMPC)Ccpcz>/Lrrc17<em1(IMPC)Ccpcz>	C57BL/6N-Lrrc17<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267036	F	MP:0001402	decreased locomotor activity	Lrrc17<em1(IMPC)Ccpcz>/Lrrc17<em1(IMPC)Ccpcz>	C57BL/6N-Lrrc17<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267037	M	MP:0010053	decreased grip strength	Lrrc4b<em1(IMPC)J>/Lrrc4b<em1(IMPC)J>	C57BL/6NJ-Lrrc4b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267042	F	MP:0004952	increased spleen weight	Mettl25<em1(IMPC)Bay>/Mettl25<em1(IMPC)Bay>	C57BL/6N-Mettl25<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267042	F	MP:0010123	increased bone mineral content	Mettl25<em1(IMPC)Bay>/Mettl25<em1(IMPC)Bay>	C57BL/6N-Mettl25<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267043	F	MP:0001297	microphthalmia	Mrps36<em1(IMPC)Bay>/Mrps36<em1(IMPC)Bay>	C57BL/6N-Mrps36<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267044	M	MP:0001402	decreased locomotor activity	Mrs2<em1(IMPC)Bay>/Mrs2<em1(IMPC)Bay>	C57BL/6N-Mrs2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267045	F	MP:0002989	small kidney	Msi2<em1(IMPC)Mbp>/Msi2<em1(IMPC)Mbp>	C57BL/6N-Msi2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267045	F	MP:0002968	increased circulating alkaline phosphatase level	Msi2<em1(IMPC)Mbp>/Msi2<em1(IMPC)Mbp>	C57BL/6N-Msi2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267045	F	MP:0002599	increased mean platelet volume	Msi2<em1(IMPC)Mbp>/Msi2<em1(IMPC)Mbp>	C57BL/6N-Msi2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267045	F	MP:0000598	abnormal liver morphology	Msi2<em1(IMPC)Mbp>/Msi2<em1(IMPC)Mbp>	C57BL/6N-Msi2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267045	F	MP:0002135	abnormal kidney morphology	Msi2<em1(IMPC)Mbp>/Msi2<em1(IMPC)Mbp>	C57BL/6N-Msi2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267045	F	MP:0002175	decreased brain weight	Msi2<em1(IMPC)Mbp>/Msi2<em1(IMPC)Mbp>	C57BL/6N-Msi2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267045	M	MP:0001552	increased circulating triglyceride level	Msi2<em1(IMPC)Mbp>/Msi2<em1(IMPC)Mbp>	C57BL/6N-Msi2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267045	M	MP:0005016	decreased lymphocyte cell number	Msi2<em1(IMPC)Mbp>/Msi2<em1(IMPC)Mbp>	C57BL/6N-Msi2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267045	F	MP:0001406	abnormal gait	Msi2<em1(IMPC)Mbp>/Msi2<em1(IMPC)Mbp>	C57BL/6N-Msi2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267045	F	MP:0003402	decreased liver weight	Msi2<em1(IMPC)Mbp>/Msi2<em1(IMPC)Mbp>	C57BL/6N-Msi2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267045	F	MP:0000601	small liver	Msi2<em1(IMPC)Mbp>/Msi2<em1(IMPC)Mbp>	C57BL/6N-Msi2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267046	F	MP:0000280	thin ventricular wall	Msx3<tm1b(EUCOMM)Wtsi>/Msx3<tm1b(EUCOMM)Wtsi>	C57BL/6N-Msx3<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:7267050	F	MP:0002941	increased circulating alanine transaminase level	Nkx2-6<em1(IMPC)H>/Nkx2-6<em1(IMPC)H>	C57BL/6NTac-Nkx2-6<em1(IMPC)H>/H	N	MGI:5576271
MGI:7267050	F	MP:0005627	increased circulating potassium level	Nkx2-6<em1(IMPC)H>/Nkx2-6<em1(IMPC)H>	C57BL/6NTac-Nkx2-6<em1(IMPC)H>/H	N	MGI:5576271
MGI:7267051	F	MP:0002941	increased circulating alanine transaminase level	Noc4l<em1(IMPC)J>/Noc4l<+>	C57BL/6NJ-Noc4l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267051	M	MP:0005343	increased circulating aspartate transaminase level	Noc4l<em1(IMPC)J>/Noc4l<+>	C57BL/6NJ-Noc4l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267055	F	MP:0002941	increased circulating alanine transaminase level	Otc<em1(IMPC)Tcp>/Otc<+>	C57BL/6NCrl-Otc<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7267055	F	MP:0000709	enlarged thymus	Otc<em1(IMPC)Tcp>/Otc<+>	C57BL/6NCrl-Otc<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7267055	F	MP:0001552	increased circulating triglyceride level	Otc<em1(IMPC)Tcp>/Otc<+>	C57BL/6NCrl-Otc<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7267057	M	MP:0001417	decreased exploration in new environment	Pcdha2<em1(IMPC)Tcp>/Pcdha2<em1(IMPC)Tcp>	C57BL/6N-Pcdha2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7267057	F	MP:0000157	abnormal sternum morphology	Pcdha2<em1(IMPC)Tcp>/Pcdha2<em1(IMPC)Tcp>	C57BL/6N-Pcdha2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7267057	M	MP:0000702	enlarged lymph nodes	Pcdha2<em1(IMPC)Tcp>/Pcdha2<em1(IMPC)Tcp>	C57BL/6N-Pcdha2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7267059	M	MP:0000220	increased monocyte cell number	Pdgfc<tm1b(EUCOMM)Hmgu>/Pdgfc<+>	C57BL/6N-Pdgfc<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:7267059	M	MP:0000322	increased granulocyte number	Pdgfc<tm1b(EUCOMM)Hmgu>/Pdgfc<+>	C57BL/6N-Pdgfc<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:7267059	F	MP:0000598	abnormal liver morphology	Pdgfc<tm1b(EUCOMM)Hmgu>/Pdgfc<+>	C57BL/6N-Pdgfc<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:7267059	F	MP:0000691	enlarged spleen	Pdgfc<tm1b(EUCOMM)Hmgu>/Pdgfc<+>	C57BL/6N-Pdgfc<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:7267059	M	MP:0010067	increased red blood cell distribution width	Pdgfc<tm1b(EUCOMM)Hmgu>/Pdgfc<+>	C57BL/6N-Pdgfc<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:7267059	M	MP:0002059	abnormal seminal vesicle morphology	Pdgfc<tm1b(EUCOMM)Hmgu>/Pdgfc<+>	C57BL/6N-Pdgfc<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:7267059	M	MP:0002135	abnormal kidney morphology	Pdgfc<tm1b(EUCOMM)Hmgu>/Pdgfc<+>	C57BL/6N-Pdgfc<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:7267060	M	MP:0005179	decreased circulating cholesterol level	Peak1<em1(IMPC)J>/Peak1<em1(IMPC)J>	C57BL/6NJ-Peak1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267060	F	MP:0005278	abnormal cholesterol homeostasis	Peak1<em1(IMPC)J>/Peak1<em1(IMPC)J>	C57BL/6NJ-Peak1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267060	M	MP:0000186	decreased circulating HDL cholesterol level	Peak1<em1(IMPC)J>/Peak1<em1(IMPC)J>	C57BL/6NJ-Peak1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267060	F	MP:0005567	decreased circulating total protein level	Peak1<em1(IMPC)J>/Peak1<em1(IMPC)J>	C57BL/6NJ-Peak1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267060	M	MP:0000195	decreased circulating calcium level	Peak1<em1(IMPC)J>/Peak1<em1(IMPC)J>	C57BL/6NJ-Peak1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267060	M	MP:0003960	increased lean body mass	Peak1<em1(IMPC)J>/Peak1<em1(IMPC)J>	C57BL/6NJ-Peak1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267060	M	MP:0001488	increased startle reflex	Peak1<em1(IMPC)J>/Peak1<em1(IMPC)J>	C57BL/6NJ-Peak1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267063	F	MP:0004156	abnormal QT variability	Phactr4<em1(IMPC)Hmgu>/Phactr4<+>	C57BL/6N-Phactr4<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7267064	M	MP:0001925	male infertility	Phf7<tm1b(EUCOMM)Hmgu>/Phf7<tm1b(EUCOMM)Hmgu>	C57BL/6N-Phf7<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7267064	M	MP:0010052	increased grip strength	Phf7<tm1b(EUCOMM)Hmgu>/Phf7<tm1b(EUCOMM)Hmgu>	C57BL/6N-Phf7<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7267065	F	MP:0001258	decreased body length	Phkg1<tm1.1(KOMP)Vlcg>/Phkg1<tm1.1(KOMP)Vlcg>	C57BL/6N-Phkg1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7267065	F	MP:0002989	small kidney	Phkg1<tm1.1(KOMP)Vlcg>/Phkg1<tm1.1(KOMP)Vlcg>	C57BL/6N-Phkg1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7267065	F	MP:0000598	abnormal liver morphology	Phkg1<tm1.1(KOMP)Vlcg>/Phkg1<tm1.1(KOMP)Vlcg>	C57BL/6N-Phkg1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7267065	F	MP:0000601	small liver	Phkg1<tm1.1(KOMP)Vlcg>/Phkg1<tm1.1(KOMP)Vlcg>	C57BL/6N-Phkg1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7267065	M	MP:0001304	cataract	Phkg1<tm1.1(KOMP)Vlcg>/Phkg1<tm1.1(KOMP)Vlcg>	C57BL/6N-Phkg1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7267067	F	MP:0002953	thick ventricular wall	Prdm15<tm1b(EUCOMM)Wtsi>/Prdm15<+>	C57BL/6N-Prdm15<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:7267067	F	MP:0010579	increased heart left ventricle size	Prdm15<tm1b(EUCOMM)Wtsi>/Prdm15<+>	C57BL/6N-Prdm15<tm1b(EUCOMM)Wtsi>/BayMmucd	N	MGI:5576271
MGI:7267068	M	MP:0010024	increased total body fat amount	Prob1<em1(IMPC)J>/Prob1<em1(IMPC)J>	C57BL/6NJ-Prob1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267070	F	MP:0009709	hydrometra	Prss47<em1(IMPC)Ccpcz>/Prss47<em1(IMPC)Ccpcz>	C57BL/6N-Prss47<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267070	M	MP:0001146	abnormal testis morphology	Prss47<em1(IMPC)Ccpcz>/Prss47<em1(IMPC)Ccpcz>	C57BL/6N-Prss47<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267070	M	MP:0001147	small testis	Prss47<em1(IMPC)Ccpcz>/Prss47<em1(IMPC)Ccpcz>	C57BL/6N-Prss47<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267070	F	MP:0002100	abnormal tooth morphology	Prss47<em1(IMPC)Ccpcz>/Prss47<em1(IMPC)Ccpcz>	C57BL/6N-Prss47<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267070	F	MP:0002339	abnormal lymph node morphology	Prss47<em1(IMPC)Ccpcz>/Prss47<em1(IMPC)Ccpcz>	C57BL/6N-Prss47<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267070	F	MP:0000703	abnormal thymus morphology	Prss47<em1(IMPC)Ccpcz>/Prss47<em1(IMPC)Ccpcz>	C57BL/6N-Prss47<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267070	F	MP:0013129	abnormal tooth color	Prss47<em1(IMPC)Ccpcz>/Prss47<em1(IMPC)Ccpcz>	C57BL/6N-Prss47<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267070	F	MP:0000702	enlarged lymph nodes	Prss47<em1(IMPC)Ccpcz>/Prss47<em1(IMPC)Ccpcz>	C57BL/6N-Prss47<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267070	F	MP:0001120	abnormal uterus morphology	Prss47<em1(IMPC)Ccpcz>/Prss47<em1(IMPC)Ccpcz>	C57BL/6N-Prss47<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267070	F	MP:0000709	enlarged thymus	Prss47<em1(IMPC)Ccpcz>/Prss47<em1(IMPC)Ccpcz>	C57BL/6N-Prss47<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267071	F	MP:0005554	decreased circulating creatinine level	Psip1<em1(IMPC)J>/Psip1<+>	C57BL/6NJ-Psip1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267073	F	MP:0010067	increased red blood cell distribution width	Pxdc1<tm1e.1(KOMP)Wtsi>/Pxdc1<tm1e.1(KOMP)Wtsi>	C57BL/6N-Pxdc1<tm1e.1(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:7267074	F	MP:0002764	short tibia	Rai2<em1(IMPC)Bay>/Rai2<em1(IMPC)Bay>	C57BL/6N-Rai2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267074	F	MP:0010579	increased heart left ventricle size	Rai2<em1(IMPC)Bay>/Rai2<em1(IMPC)Bay>	C57BL/6N-Rai2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267075	M	MP:0003961	decreased lean body mass	Rbm45<em1(IMPC)J>/Rbm45<+>	C57BL/6NJ-Rbm45<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267075	M	MP:0000063	decreased bone mineral density	Rbm45<em1(IMPC)J>/Rbm45<+>	C57BL/6NJ-Rbm45<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267075	M	MP:0010024	increased total body fat amount	Rbm45<em1(IMPC)J>/Rbm45<+>	C57BL/6NJ-Rbm45<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267076	F	MP:0001697	abnormal embryo size	Rbm48<em1(IMPC)J>/Rbm48<+>	C57BL/6NJ-Rbm48<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267078	M	MP:0000198	decreased circulating phosphate level	Rfc5<em1(IMPC)J>/Rfc5<+>	C57BL/6NJ-Rfc5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267079	M	MP:0013278	decreased fasting circulating glucose level	Rnf133<tm1.1(KOMP)Vlcg>/Rnf133<tm1.1(KOMP)Vlcg>	C57BL/6N-Rnf133<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:7267081	F	MP:0001325	abnormal retina morphology	Robo3<em1(IMPC)H>/Robo3<+>	C57BL/6NTac-Robo3<em1(IMPC)H>/H	N	MGI:5576271
MGI:7267081	M	MP:0005344	increased circulating bilirubin level	Robo3<em1(IMPC)H>/Robo3<+>	C57BL/6NTac-Robo3<em1(IMPC)H>/H	N	MGI:5576271
MGI:7267081	M	MP:0002833	increased heart weight	Robo3<em1(IMPC)H>/Robo3<+>	C57BL/6NTac-Robo3<em1(IMPC)H>/H	N	MGI:5576271
MGI:7267083	M	MP:0000598	abnormal liver morphology	Rtp4<tm1b(EUCOMM)Hmgu>/Rtp4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rtp4<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7267083	F	MP:0001399	hyperactivity	Rtp4<tm1b(EUCOMM)Hmgu>/Rtp4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rtp4<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7267083	F	MP:0002599	increased mean platelet volume	Rtp4<tm1b(EUCOMM)Hmgu>/Rtp4<tm1b(EUCOMM)Hmgu>	C57BL/6N-Rtp4<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7267085	F	MP:0005559	increased circulating glucose level	Sap30<em1(IMPC)J>/Sap30<em1(IMPC)J>	C57BL/6NJ-Sap30<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267087	F	MP:0000195	decreased circulating calcium level	Scoc<em1(IMPC)J>/Scoc<+>	C57BL/6NJ-Scoc<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267087	M	MP:0010506	prolonged RR interval	Scoc<em1(IMPC)J>/Scoc<+>	C57BL/6NJ-Scoc<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267087	M	MP:0005333	decreased heart rate	Scoc<em1(IMPC)J>/Scoc<+>	C57BL/6NJ-Scoc<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267091	M	MP:0010506	prolonged RR interval	Spa17<em1(IMPC)J>/Spa17<em1(IMPC)J>	C57BL/6NJ-Spa17<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267091	M	MP:0001925	male infertility	Spa17<em1(IMPC)J>/Spa17<em1(IMPC)J>	C57BL/6NJ-Spa17<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267091	M	MP:0005333	decreased heart rate	Spa17<em1(IMPC)J>/Spa17<em1(IMPC)J>	C57BL/6NJ-Spa17<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267092	M	MP:0010024	increased total body fat amount	Spg11<em1(IMPC)J>/Spg11<em1(IMPC)J>	C57BL/6NJ-Spg11<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267092	F	MP:0010506	prolonged RR interval	Spg11<em1(IMPC)J>/Spg11<em1(IMPC)J>	C57BL/6NJ-Spg11<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267092	F	MP:0005333	decreased heart rate	Spg11<em1(IMPC)J>/Spg11<em1(IMPC)J>	C57BL/6NJ-Spg11<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267092	F	MP:0005567	decreased circulating total protein level	Spg11<em1(IMPC)J>/Spg11<em1(IMPC)J>	C57BL/6NJ-Spg11<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267093	F	MP:0010506	prolonged RR interval	Sppl3<em1(IMPC)Bay>/Sppl3<+>	C57BL/6N-Sppl3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267094	F	MP:0003385	abnormal body wall morphology	Sppl3<em1(IMPC)Bay>/Sppl3<em1(IMPC)Bay>	C57BL/6N-Sppl3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267095	F	MP:0002591	decreased mean corpuscular volume	Sptb<em1(IMPC)J>/Sptb<+>	C57BL/6NJ-Sptb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267095	M	MP:0001417	decreased exploration in new environment	Sptb<em1(IMPC)J>/Sptb<+>	C57BL/6NJ-Sptb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267096	M	MP:0010025	decreased total body fat amount	Ssh2<em1(IMPC)J>/Ssh2<em1(IMPC)J>	C57BL/6NJ-Ssh2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267096	M	MP:0003960	increased lean body mass	Ssh2<em1(IMPC)J>/Ssh2<em1(IMPC)J>	C57BL/6NJ-Ssh2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267096	M	MP:0000218	increased leukocyte cell number	Ssh2<em1(IMPC)J>/Ssh2<em1(IMPC)J>	C57BL/6NJ-Ssh2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267096	M	MP:0005635	decreased circulating bilirubin level	Ssh2<em1(IMPC)J>/Ssh2<em1(IMPC)J>	C57BL/6NJ-Ssh2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267096	M	MP:0010123	increased bone mineral content	Ssh2<em1(IMPC)J>/Ssh2<em1(IMPC)J>	C57BL/6NJ-Ssh2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267096	M	MP:0001925	male infertility	Ssh2<em1(IMPC)J>/Ssh2<em1(IMPC)J>	C57BL/6NJ-Ssh2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267096	F	MP:0003233	prolonged QT interval	Ssh2<em1(IMPC)J>/Ssh2<em1(IMPC)J>	C57BL/6NJ-Ssh2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267097	F	MP:0001392	abnormal locomotor behavior	Stac<em1(IMPC)J>/Stac<em1(IMPC)J>	C57BL/6NJ-Stac<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267099	F	MP:0000218	increased leukocyte cell number	Swt1<em1(IMPC)J>/Swt1<em1(IMPC)J>	C57BL/6NJ-Swt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267101	F	MP:0010053	decreased grip strength	Syt8<em1(IMPC)J>/Syt8<em1(IMPC)J>	C57BL/6NJ-Syt8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267101	M	MP:0001513	limb grasping	Syt8<em1(IMPC)J>/Syt8<em1(IMPC)J>	C57BL/6NJ-Syt8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267101	F	MP:0008259	abnormal optic disk morphology	Syt8<em1(IMPC)J>/Syt8<em1(IMPC)J>	C57BL/6NJ-Syt8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267102	M	MP:0003960	increased lean body mass	Tars3<em1(IMPC)J>/Tars3<em1(IMPC)J>	C57BL/6NJ-Tars3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267102	M	MP:0005567	decreased circulating total protein level	Tars3<em1(IMPC)J>/Tars3<em1(IMPC)J>	C57BL/6NJ-Tars3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267102	F	MP:0000063	decreased bone mineral density	Tars3<em1(IMPC)J>/Tars3<em1(IMPC)J>	C57BL/6NJ-Tars3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267102	M	MP:0010025	decreased total body fat amount	Tars3<em1(IMPC)J>/Tars3<em1(IMPC)J>	C57BL/6NJ-Tars3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267102	M	MP:0005419	decreased circulating serum albumin level	Tars3<em1(IMPC)J>/Tars3<em1(IMPC)J>	C57BL/6NJ-Tars3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267102	F	MP:0005565	increased blood urea nitrogen level	Tars3<em1(IMPC)J>/Tars3<em1(IMPC)J>	C57BL/6NJ-Tars3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267103	F	MP:0001785	edema	Tbc1d32<em1(IMPC)J>/Tbc1d32<em1(IMPC)J>	C57BL/6NJ-Tbc1d32<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267103	F	MP:0001914	hemorrhage	Tbc1d32<em1(IMPC)J>/Tbc1d32<em1(IMPC)J>	C57BL/6NJ-Tbc1d32<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267104	M	MP:0004953	decreased spleen weight	Tbc1d8b<em1(IMPC)Bay>/Y	C57BL/6N-Tbc1d8b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267106	M	MP:0010506	prolonged RR interval	Tbcc<em1(IMPC)J>/Tbcc<+>	C57BL/6NJ-Tbcc<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267107	M	MP:0001148	enlarged testis	Tgds<em1(IMPC)Mbp>/Tgds<+>	C57BL/6N-Tgds<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267107	M	MP:0001364	decreased anxiety-related response	Tgds<em1(IMPC)Mbp>/Tgds<+>	C57BL/6N-Tgds<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267107	M	MP:0001399	hyperactivity	Tgds<em1(IMPC)Mbp>/Tgds<+>	C57BL/6N-Tgds<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267107	F	MP:0002092	abnormal eye morphology	Tgds<em1(IMPC)Mbp>/Tgds<+>	C57BL/6N-Tgds<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267107	M	MP:0001146	abnormal testis morphology	Tgds<em1(IMPC)Mbp>/Tgds<+>	C57BL/6N-Tgds<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267107	M	MP:0002135	abnormal kidney morphology	Tgds<em1(IMPC)Mbp>/Tgds<+>	C57BL/6N-Tgds<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267107	M	MP:0002989	small kidney	Tgds<em1(IMPC)Mbp>/Tgds<+>	C57BL/6N-Tgds<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267107	F	MP:0002792	abnormal retina vasculature morphology	Tgds<em1(IMPC)Mbp>/Tgds<+>	C57BL/6N-Tgds<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267107	M	MP:0004924	abnormal behavior	Tgds<em1(IMPC)Mbp>/Tgds<+>	C57BL/6N-Tgds<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267107	M	MP:0001402	decreased locomotor activity	Tgds<em1(IMPC)Mbp>/Tgds<+>	C57BL/6N-Tgds<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267107	M	MP:0020870	decreased thigmotaxis	Tgds<em1(IMPC)Mbp>/Tgds<+>	C57BL/6N-Tgds<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267108	F	MP:0010052	increased grip strength	Thoc3<em1(IMPC)J>/Thoc3<+>	C57BL/6NJ-Thoc3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267109	M	MP:0005293	impaired glucose tolerance	Tigd3<em1(IMPC)J>/Tigd3<em1(IMPC)J>	C57BL/6NJ-Tigd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267109	F	MP:0005343	increased circulating aspartate transaminase level	Tigd3<em1(IMPC)J>/Tigd3<em1(IMPC)J>	C57BL/6NJ-Tigd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267109	F	MP:0002941	increased circulating alanine transaminase level	Tigd3<em1(IMPC)J>/Tigd3<em1(IMPC)J>	C57BL/6NJ-Tigd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267109	M	MP:0010052	increased grip strength	Tigd3<em1(IMPC)J>/Tigd3<em1(IMPC)J>	C57BL/6NJ-Tigd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267110	M	MP:0001289	persistence of hyaloid vascular system	Tle3<em1(IMPC)Mbp>/Tle3<em1(IMPC)Mbp>	C57BL/6N-Tle3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267110	F	MP:0000689	abnormal spleen morphology	Tle3<em1(IMPC)Mbp>/Tle3<em1(IMPC)Mbp>	C57BL/6N-Tle3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267110	M	MP:0001146	abnormal testis morphology	Tle3<em1(IMPC)Mbp>/Tle3<em1(IMPC)Mbp>	C57BL/6N-Tle3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267110	F	MP:0000692	small spleen	Tle3<em1(IMPC)Mbp>/Tle3<em1(IMPC)Mbp>	C57BL/6N-Tle3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267110	M	MP:0001147	small testis	Tle3<em1(IMPC)Mbp>/Tle3<em1(IMPC)Mbp>	C57BL/6N-Tle3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267111	F	MP:0001700	abnormal embryo turning	Tlk2<em1(IMPC)Bay>/Tlk2<em1(IMPC)Bay>	C57BL/6N-Tlk2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267112	M	MP:0004953	decreased spleen weight	Tm4sf20<em1(IMPC)Bay>/Tm4sf20<em1(IMPC)Bay>	C57BL/6N-Tm4sf20<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267113	F	MP:0010053	decreased grip strength	Tnrc6b<em1(IMPC)Bay>/Tnrc6b<em1(IMPC)Bay>	C57BL/6N-Tnrc6b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267113	M	MP:0001925	male infertility	Tnrc6b<em1(IMPC)Bay>/Tnrc6b<em1(IMPC)Bay>	C57BL/6N-Tnrc6b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267113	F	MP:0020870	decreased thigmotaxis	Tnrc6b<em1(IMPC)Bay>/Tnrc6b<em1(IMPC)Bay>	C57BL/6N-Tnrc6b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267113	F	MP:0010124	decreased bone mineral content	Tnrc6b<em1(IMPC)Bay>/Tnrc6b<em1(IMPC)Bay>	C57BL/6N-Tnrc6b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267113	F	MP:0000063	decreased bone mineral density	Tnrc6b<em1(IMPC)Bay>/Tnrc6b<em1(IMPC)Bay>	C57BL/6N-Tnrc6b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267114	F	MP:0005238	increased brain size	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267114	F	MP:0002060	abnormal skin morphology	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267114	F	MP:0002792	abnormal retina vasculature morphology	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267114	F	MP:0003068	enlarged kidney	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267114	F	MP:0000689	abnormal spleen morphology	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267114	F	MP:0000598	abnormal liver morphology	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267114	M	MP:0001489	decreased startle reflex	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267114	F	MP:0000601	small liver	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267114	F	MP:0000691	enlarged spleen	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267114	M	MP:0001148	enlarged testis	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267114	F	MP:0002152	abnormal brain morphology	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267114	M	MP:0001146	abnormal testis morphology	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267114	F	MP:0002135	abnormal kidney morphology	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267114	F	MP:0002092	abnormal eye morphology	Tph2<em1(IMPC)Mbp>/Tph2<+>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267115	F	MP:0004832	enlarged ovary	Tph2<em1(IMPC)Mbp>/Tph2<em1(IMPC)Mbp>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267115	M	MP:0000691	enlarged spleen	Tph2<em1(IMPC)Mbp>/Tph2<em1(IMPC)Mbp>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267115	M	MP:0003231	abnormal placenta vasculature	Tph2<em1(IMPC)Mbp>/Tph2<em1(IMPC)Mbp>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267115	F	MP:0001417	decreased exploration in new environment	Tph2<em1(IMPC)Mbp>/Tph2<em1(IMPC)Mbp>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267115	F	MP:0001402	decreased locomotor activity	Tph2<em1(IMPC)Mbp>/Tph2<em1(IMPC)Mbp>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267115	M	MP:0001711	abnormal placenta morphology	Tph2<em1(IMPC)Mbp>/Tph2<em1(IMPC)Mbp>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267115	M	MP:0000689	abnormal spleen morphology	Tph2<em1(IMPC)Mbp>/Tph2<em1(IMPC)Mbp>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267115	F	MP:0005011	increased eosinophil cell number	Tph2<em1(IMPC)Mbp>/Tph2<em1(IMPC)Mbp>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267115	M	MP:0011110	preweaning lethality, incomplete penetrance	Tph2<em1(IMPC)Mbp>/Tph2<em1(IMPC)Mbp>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267115	F	MP:0001126	abnormal ovary morphology	Tph2<em1(IMPC)Mbp>/Tph2<em1(IMPC)Mbp>	C57BL/6N-Tph2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267117	F	MP:0001402	decreased locomotor activity	Trappc4<em1(IMPC)Bay>/Trappc4<+>	C57BL/6N-Trappc4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267120	F	MP:0010124	decreased bone mineral content	Trim46<em1(IMPC)J>/Trim46<em1(IMPC)J>	C57BL/6NJ-Trim46<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267120	F	MP:0001402	decreased locomotor activity	Trim46<em1(IMPC)J>/Trim46<em1(IMPC)J>	C57BL/6NJ-Trim46<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267120	F	MP:0002797	increased thigmotaxis	Trim46<em1(IMPC)J>/Trim46<em1(IMPC)J>	C57BL/6NJ-Trim46<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267122	M	MP:0004953	decreased spleen weight	Trim50<tm1b(KOMP)Wtsi>/Trim50<tm1b(KOMP)Wtsi>	C57BL/6N-Trim50<tm1b(KOMP)Wtsi>/BayMmucd	N	MGI:5576271
MGI:7267123	M	MP:0002941	increased circulating alanine transaminase level	Trpm2<em1(IMPC)H>/Trpm2<em1(IMPC)H>	C57BL/6N-Trpm2<em1(IMPC)H>/H	N	MGI:5576271
MGI:7267124	M	MP:0002574	increased vertical activity	Tspan7<em1(IMPC)J>/Y	C57BL/6NJ-Tspan7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267124	M	MP:0001415	increased exploration in new environment	Tspan7<em1(IMPC)J>/Y	C57BL/6NJ-Tspan7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267124	M	MP:0001399	hyperactivity	Tspan7<em1(IMPC)J>/Y	C57BL/6NJ-Tspan7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267125	F	MP:0002574	increased vertical activity	Tspan7<em1(IMPC)J>/Tspan7<em1(IMPC)J>	C57BL/6NJ-Tspan7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267125	F	MP:0001399	hyperactivity	Tspan7<em1(IMPC)J>/Tspan7<em1(IMPC)J>	C57BL/6NJ-Tspan7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267126	M	MP:0010052	increased grip strength	Ift56<em1(IMPC)J>/Ift56<+>	C57BL/6NJ-Ift56<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267128	F	MP:0010124	decreased bone mineral content	Txndc11<em1(IMPC)J>/Txndc11<em1(IMPC)J>	C57BL/6NJ-Txndc11<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267128	M	MP:0005178	increased circulating cholesterol level	Txndc11<em1(IMPC)J>/Txndc11<em1(IMPC)J>	C57BL/6NJ-Txndc11<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267128	F	MP:0003795	abnormal bone structure	Txndc11<em1(IMPC)J>/Txndc11<em1(IMPC)J>	C57BL/6NJ-Txndc11<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267130	F	MP:0005560	decreased circulating glucose level	U2surp<em1(IMPC)J>/U2surp<+>	C57BL/6NJ-U2surp<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267132	M	MP:0005568	increased circulating total protein level	Vps37b<em1(IMPC)H>/Vps37b<em1(IMPC)H>	C57BL/6NTac-Vps37b<em1(IMPC)H>/H	N	MGI:5576271
MGI:7267132	F	MP:0001392	abnormal locomotor behavior	Vps37b<em1(IMPC)H>/Vps37b<em1(IMPC)H>	C57BL/6NTac-Vps37b<em1(IMPC)H>/H	N	MGI:5576271
MGI:7267132	M	MP:0002965	increased circulating serum albumin level	Vps37b<em1(IMPC)H>/Vps37b<em1(IMPC)H>	C57BL/6NTac-Vps37b<em1(IMPC)H>/H	N	MGI:5576271
MGI:7267133	M	MP:0011100	preweaning lethality, complete penetrance	Vps54<em1(IMPC)Bay>/Vps54<em1(IMPC)Bay>	C57BL/6N-Vps54<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7267134	M	MP:0003068	enlarged kidney	Vstm2a<em1(IMPC)Mbp>/Vstm2a<em1(IMPC)Mbp>	C57BL/6N-Vstm2a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267134	F	MP:0002989	small kidney	Vstm2a<em1(IMPC)Mbp>/Vstm2a<em1(IMPC)Mbp>	C57BL/6N-Vstm2a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267134	M	MP:0003604	single kidney	Vstm2a<em1(IMPC)Mbp>/Vstm2a<em1(IMPC)Mbp>	C57BL/6N-Vstm2a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267137	M	MP:0005565	increased blood urea nitrogen level	Wiz<em1(IMPC)Ccpcz>/Wiz<+>	C57BL/6N-Wiz<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267137	F	MP:0010099	abnormal thoracic cage shape	Wiz<em1(IMPC)Ccpcz>/Wiz<+>	C57BL/6N-Wiz<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7267138	M	MP:0001289	persistence of hyaloid vascular system	Xdh<em1(IMPC)Mbp>/Xdh<+>	C57BL/6N-Xdh<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267138	F	MP:0001175	abnormal lung morphology	Xdh<em1(IMPC)Mbp>/Xdh<+>	C57BL/6N-Xdh<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267139	M	MP:0001925	male infertility	Xdh<em1(IMPC)Mbp>/Xdh<em1(IMPC)Mbp>	C57BL/6N-Xdh<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7267140	F	MP:0001566	increased circulating phosphate level	Zbtb44<em1(IMPC)J>/Zbtb44<em1(IMPC)J>	C57BL/6NJ-Zbtb44<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267141	M	MP:0010506	prolonged RR interval	Zdhhc22<em1(IMPC)J>/Zdhhc22<em1(IMPC)J>	C57BL/6NJ-Zdhhc22<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267141	F	MP:0010052	increased grip strength	Zdhhc22<em1(IMPC)J>/Zdhhc22<em1(IMPC)J>	C57BL/6NJ-Zdhhc22<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267143	M	MP:0001417	decreased exploration in new environment	Zfhx4<em1(IMPC)J>/Zfhx4<+>	C57BL/6NJ-Zfhx4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267145	M	MP:0005293	impaired glucose tolerance	Zfp462<em1(IMPC)Tcp>/Zfp462<+>	C57BL/6N-Zfp462<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7267145	M	MP:0003961	decreased lean body mass	Zfp462<em1(IMPC)Tcp>/Zfp462<+>	C57BL/6N-Zfp462<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7267145	M	MP:0010024	increased total body fat amount	Zfp462<em1(IMPC)Tcp>/Zfp462<+>	C57BL/6N-Zfp462<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7267145	M	MP:0001488	increased startle reflex	Zfp462<em1(IMPC)Tcp>/Zfp462<+>	C57BL/6N-Zfp462<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7267145	M	MP:0003179	thrombocytopenia	Zfp462<em1(IMPC)Tcp>/Zfp462<+>	C57BL/6N-Zfp462<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7267148	M	MP:0002075	abnormal coat/hair pigmentation	Zfp746<tm1b(EUCOMM)Hmgu>/Zfp746<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp746<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7267148	F	MP:0000063	decreased bone mineral density	Zfp746<tm1b(EUCOMM)Hmgu>/Zfp746<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp746<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7267148	F	MP:0010124	decreased bone mineral content	Zfp746<tm1b(EUCOMM)Hmgu>/Zfp746<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp746<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7267148	F	MP:0003961	decreased lean body mass	Zfp746<tm1b(EUCOMM)Hmgu>/Zfp746<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp746<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7267148	M	MP:0002997	enlarged seminal vesicle	Zfp746<tm1b(EUCOMM)Hmgu>/Zfp746<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp746<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7267148	F	MP:0010053	decreased grip strength	Zfp746<tm1b(EUCOMM)Hmgu>/Zfp746<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp746<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7267148	M	MP:0003960	increased lean body mass	Zfp746<tm1b(EUCOMM)Hmgu>/Zfp746<tm1b(EUCOMM)Hmgu>	C57BL/6N-Zfp746<tm1b(EUCOMM)Hmgu>/Kmpc	N	MGI:5576271
MGI:7267149	M	MP:0001402	decreased locomotor activity	Zfyve19<em1(IMPC)J>/Zfyve19<em1(IMPC)J>	C57BL/6NJ-Zfyve19<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7267150	M	MP:0010052	increased grip strength	Znhit2<em1(IMPC)J>/Znhit2<+>	C57BL/6NJ-Znhit2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7275232	F	MP:0004009	abnormal diastolic filling velocity	Rbm20<em1Hgra>/Rbm20<+>	C57BL/6-Rbm20<em1Hgra>	N	35041844
MGI:7275235	F	MP:0005389	reproductive system phenotype	Thada<em1Zsg>/Thada<em1Zsg>	C57BL/6J-Thada<em1Zsg>	Y	35480478
MGI:7276138	F	MP:0020848	abnormal exocytosis	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0004905	decreased uterus weight	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0009647	decreased fertilization frequency	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0001262	decreased body weight	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0003507	abnormal ovary physiology	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0003348	hypopituitarism	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0001926	female infertility	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	M	MP:0001922	reduced male fertility	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0003355	decreased ovulation rate	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	M	MP:0005389	reproductive system phenotype	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	Y	34135859
MGI:7276138	F	MP:0005133	increased luteinizing hormone level	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0009018	short estrus	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0009011	prolonged diestrus	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0002680	decreased corpora lutea number	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0001923	reduced female fertility	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0002773	decreased circulating luteinizing hormone level	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0001927	abnormal estrous cycle	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0005376	homeostasis/metabolism phenotype	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	Y	34135859
MGI:7276138	F	MP:0001377	abnormal mating frequency	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0001935	decreased litter size	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0005185	decreased circulating progesterone level	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0008546	abnormal vesicle-mediated transport	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0009047	short metestrus	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0005319	abnormal enzyme/coenzyme level	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0004856	decreased ovary weight	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0002636	delayed vaginal opening	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276138	F	MP:0005646	abnormal pituitary gland physiology	Mirc33<em1Smoc>/Mirc33<em1Smoc>	Not Specified	N	34135859
MGI:7276167	M	MP:0001154	seminiferous tubule degeneration	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0001925	male infertility	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0004852	decreased testis weight	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0020355	abnormal Sertoli cell barrier morphology	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0001262	decreased body weight	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	F	MP:0006380	abnormal spermatid morphology	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0020362	abnormal male germ cell physiology	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0009230	abnormal sperm head morphology	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0009257	dilated seminiferous tubule	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0020550	multinucleated giant male germ cells	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0001156	abnormal spermatogenesis	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0011632	dilated mitochondrion	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0002662	abnormal cauda epididymis morphology	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0002687	oligozoospermia	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0006379	abnormal spermatocyte morphology	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0011743	abnormal Golgi apparatus morphology	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0002675	asthenozoospermia	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0004231	abnormal calcium ion homeostasis	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0020451	decreased sperm progressive motility	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0002784	abnormal Sertoli cell morphology	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0031389	abnormal ectoplasmic specialization morphology	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	M	MP:0001932	abnormal spermiogenesis	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	N	26969191
MGI:7276167	F	MP:0005389	reproductive system phenotype	Orai1<Gt(XL922)Byg>/Orai1<Gt(XL922)Byg>	involves: 129P2/OlaHsd * ICR	Y	26969191
MGI:7276176	M	MP:0002753	dilated heart left ventricle	Rbm20<em2Hgra>/Rbm20<em2Hgra>	C57BL/6J-Rbm20<em2Hgra>	N	35394688
MGI:7276176	M	MP:0021158	decreased heart left ventricle wall thickness	Rbm20<em2Hgra>/Rbm20<em2Hgra>	C57BL/6J-Rbm20<em2Hgra>	N	35394688
MGI:7276177	M	MP:0021158	decreased heart left ventricle wall thickness	Rbm20<em2Hgra>/Rbm20<+>	C57BL/6J-Rbm20<em2Hgra>	N	35394688
MGI:7276234	M	MP:0031351	abnormal sperm flagellum thickness	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0001932	abnormal spermiogenesis	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0009834	abnormal sperm annulus morphology	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0008545	absent sperm flagellum	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0009838	abnormal sperm axoneme morphology	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0009836	abnormal sperm principal piece morphology	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0030590	abnormal sperm fibrous sheath morphology	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0009833	absent sperm mitochondrial sheath	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0031356	abnormal outer dense fiber morphology	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0001925	male infertility	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0008892	abnormal sperm flagellum morphology	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0009230	abnormal sperm head morphology	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0020869	immotile sperm	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0009831	abnormal sperm midpiece morphology	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0002687	oligozoospermia	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0030591	absent sperm fibrous sheath	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0009830	abnormal sperm connecting piece morphology	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0009239	short sperm flagellum	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0009237	kinked sperm flagellum	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	F	MP:0005389	reproductive system phenotype	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	Y	33968937
MGI:7276234	M	MP:0009238	coiled sperm flagellum	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7276234	M	MP:0009837	abnormal sperm end piece morphology	Dnah2<em1(IMPC)Tcp>/Dnah2<em1(IMPC)Tcp>	involves: C57BL/6NCrl	N	33968937
MGI:7277679	F	MP:0001129	impaired ovarian folliculogenesis	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0031383	increased secondary ovarian follicle number	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0031239	increased atretic ovarian follicle number	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0001923	reduced female fertility	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0001935	decreased litter size	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0005418	abnormal circulating hormone level	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0002680	decreased corpora lutea number	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0021106	abnormal secondary ovarian follicle morphology	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0003357	impaired granulosa cell differentiation	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0011385	abnormal testosterone level	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0011124	increased primary ovarian follicle number	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0003953	abnormal hormone level	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0031420	decreased superovulation rate	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0005319	abnormal enzyme/coenzyme level	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0009006	prolonged estrous cycle	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0002682	decreased mature ovarian follicle number	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277679	F	MP:0011128	increased tertiary ovarian follicle number	Prkaa1<tm1Sbj>/Prkaa1<tm1Sbj>	involves: 129S2/SvPas	N	35459945
MGI:7277684	F	MP:0001405	impaired coordination	Eef1a2<em#Abb>/Eef1a2<+>	C57BL/6JCrl-Eef1a2<em#Abb>	N	32160274
MGI:7277684	F	MP:0004819	decreased skeletal muscle mass	Eef1a2<em#Abb>/Eef1a2<+>	C57BL/6JCrl-Eef1a2<em#Abb>	N	32160274
MGI:7277808	M	MP:0005389	reproductive system phenotype	Tlcd3b<em1(IMPC)Bay>/Tlcd3b<em1(IMPC)Bay>	C57BL/6NJ-Tlcd3b<em1(IMPC)Bay>/Mmnc	Y	33077892
MGI:7277819	M	MP:0010357	increased prostate gland tumor incidence	Gt(ROSA)26Sor<tm1(CAG-MYCN,-luc)Jhsc>/Gt(ROSA)26Sor<+>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129 * 129S1/Sv * 129S6/SvEvTac * C57BL/6 * DBA/2	N	34099734
MGI:7277819	M	MP:0001272	increased metastatic potential	Gt(ROSA)26Sor<tm1(CAG-MYCN,-luc)Jhsc>/Gt(ROSA)26Sor<+>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129 * 129S1/Sv * 129S6/SvEvTac * C57BL/6 * DBA/2	N	34099734
MGI:7277819	M	MP:0002083	premature death	Gt(ROSA)26Sor<tm1(CAG-MYCN,-luc)Jhsc>/Gt(ROSA)26Sor<+>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pbsn-cre)4Prb/0	involves: 129 * 129S1/Sv * 129S6/SvEvTac * C57BL/6 * DBA/2	N	34099734
MGI:7277820	M	MP:0010357	increased prostate gland tumor incidence	Gt(ROSA)26Sor<tm1(CAG-MYCN,-luc)Jhsc>/Gt(ROSA)26Sor<+>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Rb1<tm2Brn>/Rb1<+>,Tg(Pbsn-cre)4Prb/0	involves: 129 * 129S1/Sv * 129S6/SvEvTac * C57BL/6 * DBA/2	N	34099734
MGI:7277820	M	MP:0002083	premature death	Gt(ROSA)26Sor<tm1(CAG-MYCN,-luc)Jhsc>/Gt(ROSA)26Sor<+>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Rb1<tm2Brn>/Rb1<+>,Tg(Pbsn-cre)4Prb/0	involves: 129 * 129S1/Sv * 129S6/SvEvTac * C57BL/6 * DBA/2	N	34099734
MGI:7277821	M	MP:0009219	increased prostate intraepithelial neoplasia incidence	Gt(ROSA)26Sor<tm1(CAG-MYCN,-luc)Jhsc>/Gt(ROSA)26Sor<+>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129 * 129S1/Sv * 129S6/SvEvTac * C57BL/6 * DBA/2	N	34099734
MGI:7277821	M	MP:0002083	premature death	Gt(ROSA)26Sor<tm1(CAG-MYCN,-luc)Jhsc>/Gt(ROSA)26Sor<+>,Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Tg(Pbsn-cre)4Prb/0	involves: 129 * 129S1/Sv * 129S6/SvEvTac * C57BL/6 * DBA/2	N	34099734
MGI:7278688	F	MP:0004514	dystocia	Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129 * C57BL/6J * FVB/NJ	N	35349646
MGI:7278688	F	MP:0005380	embryo phenotype	Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129 * C57BL/6J * FVB/NJ	Y	35349646
MGI:7278688	F	MP:0001727	abnormal embryo implantation	Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129 * C57BL/6J * FVB/NJ	N	35349646
MGI:7278688	F	MP:0002907	abnormal parturition	Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129 * C57BL/6J * FVB/NJ	N	35349646
MGI:7278688	F	MP:0001935	decreased litter size	Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129 * C57BL/6J * FVB/NJ	N	35349646
MGI:7278688	F	MP:0012008	delayed parturition	Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129 * C57BL/6J * FVB/NJ	N	35349646
MGI:7278688	F	MP:0001923	reduced female fertility	Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129 * C57BL/6J * FVB/NJ	N	35349646
MGI:7278688	F	MP:0005376	homeostasis/metabolism phenotype	Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129 * C57BL/6J * FVB/NJ	Y	35349646
MGI:7278688	F	MP:0001385	pup cannibalization	Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129 * C57BL/6J * FVB/NJ	N	35349646
MGI:7278688	F	MP:0005389	reproductive system phenotype	Lepr<tm1.1Chua>/Lepr<tm1.1Chua>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129 * C57BL/6J * FVB/NJ	Y	35349646
MGI:7278719	F	MP:0001926	female infertility	Bcas2<tm1.1Lil>/Bcas2<tm1.1Lil>,Tg(Ddx4-cre)1Ptch/0	Not Specified	N	34972250
MGI:7278719	F	MP:0001129	impaired ovarian folliculogenesis	Bcas2<tm1.1Lil>/Bcas2<tm1.1Lil>,Tg(Ddx4-cre)1Ptch/0	Not Specified	N	34972250
MGI:7278719	F	MP:0031383	increased secondary ovarian follicle number	Bcas2<tm1.1Lil>/Bcas2<tm1.1Lil>,Tg(Ddx4-cre)1Ptch/0	Not Specified	N	34972250
MGI:7278719	F	MP:0001127	small ovary	Bcas2<tm1.1Lil>/Bcas2<tm1.1Lil>,Tg(Ddx4-cre)1Ptch/0	Not Specified	N	34972250
MGI:7278719	F	MP:0005168	abnormal female meiosis	Bcas2<tm1.1Lil>/Bcas2<tm1.1Lil>,Tg(Ddx4-cre)1Ptch/0	Not Specified	N	34972250
MGI:7278719	F	MP:0000242	impaired fertilization	Bcas2<tm1.1Lil>/Bcas2<tm1.1Lil>,Tg(Ddx4-cre)1Ptch/0	Not Specified	N	34972250
MGI:7278719	F	MP:0011124	increased primary ovarian follicle number	Bcas2<tm1.1Lil>/Bcas2<tm1.1Lil>,Tg(Ddx4-cre)1Ptch/0	Not Specified	N	34972250
MGI:7278719	F	MP:0001931	abnormal oogenesis	Bcas2<tm1.1Lil>/Bcas2<tm1.1Lil>,Tg(Ddx4-cre)1Ptch/0	Not Specified	N	34972250
MGI:7278719	F	MP:0031420	decreased superovulation rate	Bcas2<tm1.1Lil>/Bcas2<tm1.1Lil>,Tg(Ddx4-cre)1Ptch/0	Not Specified	N	34972250
MGI:7278719	F	MP:0001125	abnormal oocyte morphology	Bcas2<tm1.1Lil>/Bcas2<tm1.1Lil>,Tg(Ddx4-cre)1Ptch/0	Not Specified	N	34972250
MGI:7278719	F	MP:0011129	decreased tertiary ovarian follicle number	Bcas2<tm1.1Lil>/Bcas2<tm1.1Lil>,Tg(Ddx4-cre)1Ptch/0	Not Specified	N	34972250
MGI:7278803	M	MP:0005389	reproductive system phenotype	Ptchd3<tm1a(KOMP)Wtsi>/Ptchd3<tm1a(KOMP)Wtsi>	involves: C57BL/6N	Y	34493359
MGI:7279155	F	MP:0009664	abnormal luminal closure	Pgr<tm2(cre)Lyd>/Pgr<+>,Cripto<tm2.2Mms>/Cripto<tm2.2Mms>	involves: 129/Sv * C57BL/6N * CD-1	N	33590845
MGI:7279155	F	MP:0009360	endometrium inflammation	Pgr<tm2(cre)Lyd>/Pgr<+>,Cripto<tm2.2Mms>/Cripto<tm2.2Mms>	involves: 129/Sv * C57BL/6N * CD-1	N	33590845
MGI:7279155	F	MP:0001728	failure of embryo implantation	Pgr<tm2(cre)Lyd>/Pgr<+>,Cripto<tm2.2Mms>/Cripto<tm2.2Mms>	involves: 129/Sv * C57BL/6N * CD-1	N	33590845
MGI:7279155	F	MP:0009094	abnormal endometrial gland morphology	Pgr<tm2(cre)Lyd>/Pgr<+>,Cripto<tm2.2Mms>/Cripto<tm2.2Mms>	involves: 129/Sv * C57BL/6N * CD-1	N	33590845
MGI:7279155	F	MP:0009649	delayed embryo implantation	Pgr<tm2(cre)Lyd>/Pgr<+>,Cripto<tm2.2Mms>/Cripto<tm2.2Mms>	involves: 129/Sv * C57BL/6N * CD-1	N	33590845
MGI:7279155	F	MP:0009661	abnormal pregnancy	Pgr<tm2(cre)Lyd>/Pgr<+>,Cripto<tm2.2Mms>/Cripto<tm2.2Mms>	involves: 129/Sv * C57BL/6N * CD-1	N	33590845
MGI:7279155	F	MP:0004014	abnormal uterine environment	Pgr<tm2(cre)Lyd>/Pgr<+>,Cripto<tm2.2Mms>/Cripto<tm2.2Mms>	involves: 129/Sv * C57BL/6N * CD-1	N	33590845
MGI:7279155	F	MP:0003845	abnormal decidualization	Pgr<tm2(cre)Lyd>/Pgr<+>,Cripto<tm2.2Mms>/Cripto<tm2.2Mms>	involves: 129/Sv * C57BL/6N * CD-1	N	33590845
MGI:7279155	F	MP:0001926	female infertility	Pgr<tm2(cre)Lyd>/Pgr<+>,Cripto<tm2.2Mms>/Cripto<tm2.2Mms>	involves: 129/Sv * C57BL/6N * CD-1	N	33590845
MGI:7279155	F	MP:0009663	abnormal uterine-embryonic axis	Pgr<tm2(cre)Lyd>/Pgr<+>,Cripto<tm2.2Mms>/Cripto<tm2.2Mms>	involves: 129/Sv * C57BL/6N * CD-1	N	33590845
MGI:7279155	F	MP:0001923	reduced female fertility	Pgr<tm2(cre)Lyd>/Pgr<+>,Cripto<tm2.2Mms>/Cripto<tm2.2Mms>	involves: 129/Sv * C57BL/6N * CD-1	N	33590845
MGI:7279155	F	MP:0001935	decreased litter size	Pgr<tm2(cre)Lyd>/Pgr<+>,Cripto<tm2.2Mms>/Cripto<tm2.2Mms>	involves: 129/Sv * C57BL/6N * CD-1	N	33590845
MGI:7279155	F	MP:0009666	abnormal embryo attachment	Pgr<tm2(cre)Lyd>/Pgr<+>,Cripto<tm2.2Mms>/Cripto<tm2.2Mms>	involves: 129/Sv * C57BL/6N * CD-1	N	33590845
MGI:7279298	F	MP:0000662	abnormal branching of the mammary ductal tree	Brca2<tm2.1Sks>/Brca2<tm1Brd>	B6.Cg-Brca2<tm1Brd> Brca2<tm2.1Sks>	N	35365640
MGI:7279298	F	MP:0031174	decreased mammary duct terminal end bud number	Brca2<tm2.1Sks>/Brca2<tm1Brd>	B6.Cg-Brca2<tm1Brd> Brca2<tm2.1Sks>	N	35365640
MGI:7279298	F	MP:0005386	behavior/neurological phenotype	Brca2<tm2.1Sks>/Brca2<tm1Brd>	B6.Cg-Brca2<tm1Brd> Brca2<tm2.1Sks>	Y	35365640
MGI:7280653	F	MP:0009009	absent estrous cycle	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280653	F	MP:0001129	impaired ovarian folliculogenesis	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280653	F	MP:0001926	female infertility	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280653	F	MP:0001125	abnormal oocyte morphology	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280653	F	MP:0009093	oocyte degeneration	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280653	F	MP:0001750	increased circulating follicle stimulating hormone level	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280653	F	MP:0001127	small ovary	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280653	F	MP:0003507	abnormal ovary physiology	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280653	F	MP:0011124	increased primary ovarian follicle number	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280653	F	MP:0011130	absent tertiary ovarian follicles	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280653	F	MP:0021106	abnormal secondary ovarian follicle morphology	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280653	F	MP:0031381	decreased secondary ovarian follicle number	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280653	F	MP:0005418	abnormal circulating hormone level	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280653	F	MP:0001132	absent mature ovarian follicles	Tg(Zp3-cre)93Knw/0,Yy1<tm1Yshi>/Yy1<tm2.1Yshi>	involves: 129S4/SvJae * C57BL/6J	N	21123818
MGI:7280686	F	MP:0004856	decreased ovary weight	Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd	N	18703422
MGI:7280686	F	MP:0031420	decreased superovulation rate	Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd	N	18703422
MGI:7280686	F	MP:0005158	ovary hypoplasia	Nr5a1<tm1Klp>/Nr5a1<tm2Klp>	involves: 129P2/OlaHsd	N	18703422
MGI:7280785	F	MP:0011902	increased hematopoietic stem cell proliferation	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0005089	decreased double-negative T cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0000240	extramedullary hematopoiesis	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0000333	decreased bone marrow cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0000321	increased bone marrow cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0008254	increased megakaryocyte cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0002417	abnormal megakaryocyte morphology	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0008186	increased pro-B cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0013697	decreased granulocyte monocyte progenitor cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0013762	abnormal effector T cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0008827	abnormal thymus cell ratio	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0008826	abnormal splenic cell ratio	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0005016	decreased lymphocyte cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0005390	skeleton phenotype	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	Y	31395598
MGI:7280785	F	MP:0003179	thrombocytopenia	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0004810	decreased hematopoietic stem cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0004809	increased hematopoietic stem cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0005387	immune system phenotype	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	Y	31395598
MGI:7280785	F	MP:0000691	enlarged spleen	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0000218	increased leukocyte cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280785	F	MP:0005014	increased B cell number	Phf6<em1Wencc>/Phf6<em1Wencc>,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0008186	increased pro-B cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0005089	decreased double-negative T cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0000691	enlarged spleen	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0003179	thrombocytopenia	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0004809	increased hematopoietic stem cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0002417	abnormal megakaryocyte morphology	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0005387	immune system phenotype	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	Y	31395598
MGI:7280786	M	MP:0005390	skeleton phenotype	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	Y	31395598
MGI:7280786	M	MP:0004810	decreased hematopoietic stem cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0008254	increased megakaryocyte cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0005014	increased B cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0008826	abnormal splenic cell ratio	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0013762	abnormal effector T cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0005397	hematopoietic system phenotype	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	Y	31395598
MGI:7280786	M	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0008827	abnormal thymus cell ratio	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0000333	decreased bone marrow cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0000321	increased bone marrow cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0011902	increased hematopoietic stem cell proliferation	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0005016	decreased lymphocyte cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0013697	decreased granulocyte monocyte progenitor cell number	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280786	M	MP:0000240	extramedullary hematopoiesis	Phf6<em1Wencc>/Y,Tg(Vav1-cre)#Cgp/0	Not Specified	N	31395598
MGI:7280898	M	MP:0003887	increased hepatocyte apoptosis	Krt18<tm1Tmm>/Krt18<tm1Tmm>	involves: 129P2/OlaHsd	N	27689336
MGI:7281069	M	MP:0002675	asthenozoospermia	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	N	34255152
MGI:7281069	M	MP:0003631	nervous system phenotype	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	Y	34255152
MGI:7281069	M	MP:0002687	oligozoospermia	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	N	34255152
MGI:7281069	M	MP:0031356	abnormal outer dense fiber morphology	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	N	34255152
MGI:7281069	M	MP:0009647	decreased fertilization frequency	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	N	34255152
MGI:7281069	M	MP:0009237	kinked sperm flagellum	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	N	34255152
MGI:7281069	M	MP:0009838	abnormal sperm axoneme morphology	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	N	34255152
MGI:7281069	M	MP:0001925	male infertility	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	N	34255152
MGI:7281069	M	MP:0020451	decreased sperm progressive motility	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	N	34255152
MGI:7281069	M	MP:0009239	short sperm flagellum	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	N	34255152
MGI:7281069	M	MP:0031352	absent sperm axonemal central pair	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	N	34255152
MGI:7281069	M	MP:0009238	coiled sperm flagellum	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	N	34255152
MGI:7281069	F	MP:0005389	reproductive system phenotype	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	Y	34255152
MGI:7281069	M	MP:0008545	absent sperm flagellum	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	N	34255152
MGI:7281069	M	MP:0008892	abnormal sperm flagellum morphology	Cfap206<em1Yxc>/Cfap206<em1Yxc>	C57BL/6-Cfap206<em1Yxc>	N	34255152
MGI:7281185	F	MP:0000255	blood vessel congestion	Edn2<tm1Ywa>/Edn2<tm1Ywa>	involves: 129S6/SvEvTac * C57BL/6	N	24763822
MGI:7281185	F	MP:0031420	decreased superovulation rate	Edn2<tm1Ywa>/Edn2<tm1Ywa>	involves: 129S6/SvEvTac * C57BL/6	N	24763822
MGI:7281185	F	MP:0005185	decreased circulating progesterone level	Edn2<tm1Ywa>/Edn2<tm1Ywa>	involves: 129S6/SvEvTac * C57BL/6	N	24763822
MGI:7281185	F	MP:0001133	impaired luteal cell differentiation	Edn2<tm1Ywa>/Edn2<tm1Ywa>	involves: 129S6/SvEvTac * C57BL/6	N	24763822
MGI:7281185	F	MP:0001134	absent corpus luteum	Edn2<tm1Ywa>/Edn2<tm1Ywa>	involves: 129S6/SvEvTac * C57BL/6	N	24763822
MGI:7281185	F	MP:0001127	small ovary	Edn2<tm1Ywa>/Edn2<tm1Ywa>	involves: 129S6/SvEvTac * C57BL/6	N	24763822
MGI:7281185	F	MP:0013609	abnormal ovarian medulla morphology	Edn2<tm1Ywa>/Edn2<tm1Ywa>	involves: 129S6/SvEvTac * C57BL/6	N	24763822
MGI:7281185	F	MP:0002637	small uterus	Edn2<tm1Ywa>/Edn2<tm1Ywa>	involves: 129S6/SvEvTac * C57BL/6	N	24763822
MGI:7281308	M	MP:0020356	abnormal Sertoli cell barrier function	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0005250	decreased Sertoli cell number	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0006428	ectopic Sertoli cells	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0001147	small testis	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0014052	increased male germ cell apoptosis	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0001154	seminiferous tubule degeneration	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0031406	decreased Sertoli cell proliferation	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0020355	abnormal Sertoli cell barrier morphology	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0004852	decreased testis weight	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0004901	decreased male germ cell number	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0001155	arrest of spermatogenesis	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0004109	abnormal Sertoli cell development	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0008877	abnormal DNA methylation	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0003077	abnormal cell cycle	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0004930	small epididymis	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0002784	abnormal Sertoli cell morphology	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0001925	male infertility	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281308	M	MP:0001153	small seminiferous tubules	Uhrf1<tm1Smoc>/Uhrf1<tm1Smoc>,Tg(Amh-cre)8815Reb/0	involves: C57BL/6J * FVB/N	N	35440090
MGI:7281440	M	MP:0009647	decreased fertilization frequency	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0020451	decreased sperm progressive motility	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0004852	decreased testis weight	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0002675	asthenozoospermia	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0008279	arrest of spermiogenesis	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0009831	abnormal sperm midpiece morphology	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0006379	abnormal spermatocyte morphology	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0002687	oligozoospermia	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0002216	abnormal seminiferous tubule morphology	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0000242	impaired fertilization	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0014052	increased male germ cell apoptosis	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0030978	impaired binding of sperm to zona pellucida	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0001147	small testis	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0001925	male infertility	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281440	M	MP:0009237	kinked sperm flagellum	Ppp4c<em1Qys>/Ppp4c<em1Qys>,Tg(Stra8-icre)1Reb/0	involves: 129S/SvEv * C57BL/6 * FVB/NJ	N	33543287
MGI:7281502	M	MP:0001152	increased Leydig cell number	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281502	M	MP:0001153	small seminiferous tubules	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281502	M	MP:0001154	seminiferous tubule degeneration	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281502	M	MP:0001155	arrest of spermatogenesis	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281502	M	MP:0004901	decreased male germ cell number	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281502	M	MP:0006378	abnormal spermatogonia morphology	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281502	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281502	M	MP:0006379	abnormal spermatocyte morphology	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281502	M	MP:0020356	abnormal Sertoli cell barrier function	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281502	M	MP:0005159	azoospermia	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281502	M	MP:0020355	abnormal Sertoli cell barrier morphology	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281502	M	MP:0001925	male infertility	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281502	M	MP:0014052	increased male germ cell apoptosis	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281502	M	MP:0004852	decreased testis weight	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281516	M	MP:0001154	seminiferous tubule degeneration	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Inha-cre)3Zuk/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281516	M	MP:0001147	small testis	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Inha-cre)3Zuk/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281516	M	MP:0001925	male infertility	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Inha-cre)3Zuk/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7281516	M	MP:0001155	arrest of spermatogenesis	Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Inha-cre)3Zuk/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26265072
MGI:7282036	F	MP:0003507	abnormal ovary physiology	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0001935	decreased litter size	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0005418	abnormal circulating hormone level	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0030089	short lower incisors	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0009010	abnormal diestrus	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0009011	prolonged diestrus	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0003953	abnormal hormone level	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0011129	decreased tertiary ovarian follicle number	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0021106	abnormal secondary ovarian follicle morphology	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0030090	short upper incisors	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0001923	reduced female fertility	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0011124	increased primary ovarian follicle number	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0001927	abnormal estrous cycle	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0009020	prolonged metestrus	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0005376	homeostasis/metabolism phenotype	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	Y	34333627
MGI:7282036	F	MP:0001868	ovary inflammation	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0002680	decreased corpora lutea number	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282036	F	MP:0009018	short estrus	Grem2<em1Stpg>/Grem2<em1Stpg>	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	N	34333627
MGI:7282037	M	MP:0001155	arrest of spermatogenesis	Hsf2bp<em2Amp>/Hsf2bp<em2Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282037	M	MP:0002687	oligozoospermia	Hsf2bp<em2Amp>/Hsf2bp<em2Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282037	M	MP:0001147	small testis	Hsf2bp<em2Amp>/Hsf2bp<em2Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282037	M	MP:0005169	abnormal male meiosis	Hsf2bp<em2Amp>/Hsf2bp<em2Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282037	F	MP:0001923	reduced female fertility	Hsf2bp<em2Amp>/Hsf2bp<em2Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282037	F	MP:0001935	decreased litter size	Hsf2bp<em2Amp>/Hsf2bp<em2Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282042	F	MP:0031381	decreased secondary ovarian follicle number	Hsf2bp<em1Amp>/Hsf2bp<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282042	M	MP:0005159	azoospermia	Hsf2bp<em1Amp>/Hsf2bp<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282042	F	MP:0011125	decreased primary ovarian follicle number	Hsf2bp<em1Amp>/Hsf2bp<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282042	M	MP:0001155	arrest of spermatogenesis	Hsf2bp<em1Amp>/Hsf2bp<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282042	M	MP:0006379	abnormal spermatocyte morphology	Hsf2bp<em1Amp>/Hsf2bp<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282042	M	MP:0001147	small testis	Hsf2bp<em1Amp>/Hsf2bp<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282042	F	MP:0005168	abnormal female meiosis	Hsf2bp<em1Amp>/Hsf2bp<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282042	F	MP:0009451	abnormal chromosomal synapsis	Hsf2bp<em1Amp>/Hsf2bp<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282042	F	MP:0008871	abnormal ovarian follicle number	Hsf2bp<em1Amp>/Hsf2bp<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282042	F	MP:0011121	decreased primordial ovarian follicle number	Hsf2bp<em1Amp>/Hsf2bp<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282042	F	MP:0011129	decreased tertiary ovarian follicle number	Hsf2bp<em1Amp>/Hsf2bp<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282046	M	MP:0005159	azoospermia	Brme1<em1Amp>/Brme1<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282046	F	MP:0008871	abnormal ovarian follicle number	Brme1<em1Amp>/Brme1<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282046	M	MP:0001147	small testis	Brme1<em1Amp>/Brme1<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282046	M	MP:0001925	male infertility	Brme1<em1Amp>/Brme1<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282046	M	MP:0005169	abnormal male meiosis	Brme1<em1Amp>/Brme1<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282046	M	MP:0001155	arrest of spermatogenesis	Brme1<em1Amp>/Brme1<em1Amp>	involves: C57BL/6J * CBA/J	N	32845237
MGI:7282305	M	MP:0000519	hydronephrosis	Avpr2<tm2.1Jwe>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129 * C57BL/6	N	19729836
MGI:7282305	M	MP:0005528	decreased renal glomerular filtration rate	Avpr2<tm2.1Jwe>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129 * C57BL/6	N	19729836
MGI:7282305	M	MP:0011467	decreased urine urea nitrogen level	Avpr2<tm2.1Jwe>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129 * C57BL/6	N	19729836
MGI:7282305	M	MP:0002988	decreased urine osmolality	Avpr2<tm2.1Jwe>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129 * C57BL/6	N	19729836
MGI:7282305	M	MP:0001262	decreased body weight	Avpr2<tm2.1Jwe>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129 * C57BL/6	N	19729836
MGI:7282305	M	MP:0011471	decreased urine creatinine level	Avpr2<tm2.1Jwe>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129 * C57BL/6	N	19729836
MGI:7282305	M	MP:0001762	polyuria	Avpr2<tm2.1Jwe>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129 * C57BL/6	N	19729836
MGI:7282305	M	MP:0005618	decreased urine potassium level	Avpr2<tm2.1Jwe>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129 * C57BL/6	N	19729836
MGI:7282305	M	MP:0006317	decreased urine sodium level	Avpr2<tm2.1Jwe>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129 * C57BL/6	N	19729836
MGI:7282305	M	MP:0001426	polydipsia	Avpr2<tm2.1Jwe>/Y,Tg(CAG-cre/Esr1*)5Amc/0	involves: 129 * C57BL/6	N	19729836
MGI:7284072	F	MP:0009761	abnormal meiotic spindle morphology	Aurka<tm1c(EUCOMM)Hmgu>/Aurka<tm1c(EUCOMM)Hmgu>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	33901174
MGI:7284072	F	MP:0002680	decreased corpora lutea number	Aurka<tm1c(EUCOMM)Hmgu>/Aurka<tm1c(EUCOMM)Hmgu>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	33901174
MGI:7284072	F	MP:0010767	abnormal female meiosis I arrest	Aurka<tm1c(EUCOMM)Hmgu>/Aurka<tm1c(EUCOMM)Hmgu>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	33901174
MGI:7284072	F	MP:0001926	female infertility	Aurka<tm1c(EUCOMM)Hmgu>/Aurka<tm1c(EUCOMM)Hmgu>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	33901174
MGI:7284245	F	MP:0000662	abnormal branching of the mammary ductal tree	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0002680	decreased corpora lutea number	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0031381	decreased secondary ovarian follicle number	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0009505	abnormal mammary gland lobule morphology	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0013278	decreased fasting circulating glucose level	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0013772	increased effector memory T-helper cell number	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0000702	enlarged lymph nodes	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0009011	prolonged diestrus	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0021029	increased tumor necrosis factor (ligand) superfamily member 11 level	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0001927	abnormal estrous cycle	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0012075	impaired mammary gland growth during pregnancy	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0005186	increased circulating progesterone level	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0000628	abnormal mammary gland development	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0005331	insulin resistance	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0002079	increased circulating insulin level	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0008976	delayed female fertility	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0006082	CNS inflammation	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0002773	decreased circulating luteinizing hormone level	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0009080	uterus inflammation	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0020448	increased microglial cell activation	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0001923	reduced female fertility	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0009018	short estrus	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0005425	increased macrophage cell number	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284245	F	MP:0021032	increased tumor necrosis factor receptor superfamily member 11b level	Tnfaip3<m1Apb>/Tnfaip3<m1Apb>	C57BL/6-Tnfaip3<m1Apb>	N	35464428
MGI:7284367	M	MP:0001155	arrest of spermatogenesis	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0002631	abnormal epididymis morphology	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0001147	small testis	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0001935	decreased litter size	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0005250	decreased Sertoli cell number	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0020362	abnormal male germ cell physiology	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0001925	male infertility	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0003205	testicular atrophy	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0004929	decreased epididymis weight	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0001154	seminiferous tubule degeneration	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0014052	increased male germ cell apoptosis	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0002687	oligozoospermia	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0020355	abnormal Sertoli cell barrier morphology	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0004930	small epididymis	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0002780	decreased circulating testosterone level	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0003830	abnormal testis development	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0013600	testis degeneration	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0004852	decreased testis weight	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0006428	ectopic Sertoli cells	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0002784	abnormal Sertoli cell morphology	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0004901	decreased male germ cell number	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284367	M	MP:0001922	reduced male fertility	Fbxw7<tm1Iaai>/Fbxw7<tm1Iaai>,Tg(Amh-cre)8815Reb/0	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	N	31883011
MGI:7284681	M	MP:0001925	male infertility	Rfx2<tm1.1Wrth>/Rfx2<tm1.1Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26162102
MGI:7284681	F	MP:0005389	reproductive system phenotype	Rfx2<tm1.1Wrth>/Rfx2<tm1.1Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	Y	26162102
MGI:7284681	M	MP:0011743	abnormal Golgi apparatus morphology	Rfx2<tm1.1Wrth>/Rfx2<tm1.1Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26162102
MGI:7284681	M	MP:0008279	arrest of spermiogenesis	Rfx2<tm1.1Wrth>/Rfx2<tm1.1Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26162102
MGI:7284681	M	MP:0009377	ectopic manchette	Rfx2<tm1.1Wrth>/Rfx2<tm1.1Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26162102
MGI:7284681	M	MP:0002662	abnormal cauda epididymis morphology	Rfx2<tm1.1Wrth>/Rfx2<tm1.1Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26162102
MGI:7284681	M	MP:0031354	abnormal acrosome assembly	Rfx2<tm1.1Wrth>/Rfx2<tm1.1Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26162102
MGI:7284681	M	MP:0031389	abnormal ectoplasmic specialization morphology	Rfx2<tm1.1Wrth>/Rfx2<tm1.1Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26162102
MGI:7284681	M	MP:0020550	multinucleated giant male germ cells	Rfx2<tm1.1Wrth>/Rfx2<tm1.1Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26162102
MGI:7284681	M	MP:0001147	small testis	Rfx2<tm1.1Wrth>/Rfx2<tm1.1Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26162102
MGI:7284681	M	MP:0009231	detached acrosome	Rfx2<tm1.1Wrth>/Rfx2<tm1.1Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26162102
MGI:7284681	M	MP:0008898	abnormal acrosome morphology	Rfx2<tm1.1Wrth>/Rfx2<tm1.1Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26162102
MGI:7284681	M	MP:0009838	abnormal sperm axoneme morphology	Rfx2<tm1.1Wrth>/Rfx2<tm1.1Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	N	26162102
MGI:7284682	M	MP:0009838	abnormal sperm axoneme morphology	Rfx2<tm1.2Wrth>/Rfx2<tm1.2Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	26162102
MGI:7284682	M	MP:0008898	abnormal acrosome morphology	Rfx2<tm1.2Wrth>/Rfx2<tm1.2Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	26162102
MGI:7284682	M	MP:0009377	ectopic manchette	Rfx2<tm1.2Wrth>/Rfx2<tm1.2Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	26162102
MGI:7284682	M	MP:0001147	small testis	Rfx2<tm1.2Wrth>/Rfx2<tm1.2Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	26162102
MGI:7284682	M	MP:0008279	arrest of spermiogenesis	Rfx2<tm1.2Wrth>/Rfx2<tm1.2Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	26162102
MGI:7284682	M	MP:0009231	detached acrosome	Rfx2<tm1.2Wrth>/Rfx2<tm1.2Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	26162102
MGI:7284682	M	MP:0011743	abnormal Golgi apparatus morphology	Rfx2<tm1.2Wrth>/Rfx2<tm1.2Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	26162102
MGI:7284682	M	MP:0020550	multinucleated giant male germ cells	Rfx2<tm1.2Wrth>/Rfx2<tm1.2Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	26162102
MGI:7284682	M	MP:0001925	male infertility	Rfx2<tm1.2Wrth>/Rfx2<tm1.2Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	26162102
MGI:7284682	F	MP:0005389	reproductive system phenotype	Rfx2<tm1.2Wrth>/Rfx2<tm1.2Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	Y	26162102
MGI:7284682	M	MP:0002662	abnormal cauda epididymis morphology	Rfx2<tm1.2Wrth>/Rfx2<tm1.2Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	26162102
MGI:7284682	M	MP:0031389	abnormal ectoplasmic specialization morphology	Rfx2<tm1.2Wrth>/Rfx2<tm1.2Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	26162102
MGI:7284682	M	MP:0031354	abnormal acrosome assembly	Rfx2<tm1.2Wrth>/Rfx2<tm1.2Wrth>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	N	26162102
MGI:7284944	F	MP:0003141	cardiac fibrosis	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0005014	increased B cell number	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0004771	increased anti-single stranded DNA antibody level	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0002083	premature death	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0004794	increased anti-nuclear antigen antibody level	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0004801	increased susceptibility to systemic lupus erythematosus	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0008481	increased spleen germinal center number	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0001861	lung inflammation	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0000221	decreased leukocyte cell number	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0003865	lymph node inflammation	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0009318	increased splenic marginal zone lymphoma incidence	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0002108	abnormal muscle morphology	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0001860	liver inflammation	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0001869	pancreas inflammation	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0001870	salivary gland inflammation	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0000696	abnormal Peyer's patch morphology	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0000693	spleen hyperplasia	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0001846	increased inflammatory response	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0008182	decreased marginal zone B cell number	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0008769	abnormal plasmacytoid dendritic cell physiology	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0008074	increased CD4-positive, alpha-beta T cell number	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0002743	glomerulonephritis	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0008177	increased germinal center B cell number	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0005220	abnormal exocrine pancreas morphology	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0008171	abnormal mature B cell morphology	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0010186	increased T follicular helper cell number	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0000691	enlarged spleen	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284944	F	MP:0008097	increased plasma cell number	Tlr7<em2Anu>/Tlr7<em2Anu>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0000693	spleen hyperplasia	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0002083	premature death	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0008596	increased circulating interleukin-6 level	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0004794	increased anti-nuclear antigen antibody level	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0008577	increased circulating interferon-gamma level	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0004771	increased anti-single stranded DNA antibody level	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0011353	expanded mesangial matrix	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0008097	increased plasma cell number	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0003725	increased autoantibody level	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0008553	increased circulating tumor necrosis factor level	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0008171	abnormal mature B cell morphology	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0005014	increased B cell number	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0008074	increased CD4-positive, alpha-beta T cell number	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0008593	increased circulating interleukin-10 level	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0008481	increased spleen germinal center number	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0010186	increased T follicular helper cell number	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0003179	thrombocytopenia	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0000691	enlarged spleen	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0008177	increased germinal center B cell number	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0008769	abnormal plasmacytoid dendritic cell physiology	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0008182	decreased marginal zone B cell number	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0004762	increased anti-double stranded DNA antibody level	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284974	F	MP:0020519	renal glomerular immunoglobulin deposits	Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0001860	liver inflammation	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0008783	decreased B cell apoptosis	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0002451	abnormal macrophage physiology	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0008553	increased circulating tumor necrosis factor level	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0002459	abnormal B cell physiology	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0003141	cardiac fibrosis	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0008593	increased circulating interleukin-10 level	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0000696	abnormal Peyer's patch morphology	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0008596	increased circulating interleukin-6 level	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0005093	decreased B cell proliferation	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0009318	increased splenic marginal zone lymphoma incidence	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0002108	abnormal muscle morphology	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0003865	lymph node inflammation	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0002083	premature death	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0004794	increased anti-nuclear antigen antibody level	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0003725	increased autoantibody level	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0008074	increased CD4-positive, alpha-beta T cell number	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0004762	increased anti-double stranded DNA antibody level	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0000691	enlarged spleen	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0004801	increased susceptibility to systemic lupus erythematosus	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0008577	increased circulating interferon-gamma level	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0010186	increased T follicular helper cell number	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0001861	lung inflammation	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284986	M	MP:0004771	increased anti-single stranded DNA antibody level	Tlr7<em2Anu>/Y	C57BL/6NCrl-Tlr7<em2Anu>	N	35477763
MGI:7284994	F	MP:0008097	increased plasma cell number	Rnaseh2b<em1Anu>/Rnaseh2b<+>,Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Rnaseh2b<em1Anu> Tlr7<em2Anu>	N	35477763
MGI:7284994	F	MP:0008171	abnormal mature B cell morphology	Rnaseh2b<em1Anu>/Rnaseh2b<+>,Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Rnaseh2b<em1Anu> Tlr7<em2Anu>	N	35477763
MGI:7284994	F	MP:0008177	increased germinal center B cell number	Rnaseh2b<em1Anu>/Rnaseh2b<+>,Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Rnaseh2b<em1Anu> Tlr7<em2Anu>	N	35477763
MGI:7284994	F	MP:0010186	increased T follicular helper cell number	Rnaseh2b<em1Anu>/Rnaseh2b<+>,Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Rnaseh2b<em1Anu> Tlr7<em2Anu>	N	35477763
MGI:7284994	F	MP:0000685	abnormal immune system morphology	Rnaseh2b<em1Anu>/Rnaseh2b<+>,Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Rnaseh2b<em1Anu> Tlr7<em2Anu>	N	35477763
MGI:7284994	F	MP:0008074	increased CD4-positive, alpha-beta T cell number	Rnaseh2b<em1Anu>/Rnaseh2b<+>,Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Rnaseh2b<em1Anu> Tlr7<em2Anu>	N	35477763
MGI:7284994	F	MP:0003725	increased autoantibody level	Rnaseh2b<em1Anu>/Rnaseh2b<+>,Tlr7<em2Anu>/Tlr7<+>	C57BL/6NCrl-Rnaseh2b<em1Anu> Tlr7<em2Anu>	N	35477763
MGI:7285921	M	MP:0001156	abnormal spermatogenesis	Usp9x<tm1Tuv>/Y,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	28559472
MGI:7285921	M	MP:0001932	abnormal spermiogenesis	Usp9x<tm1Tuv>/Y,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	28559472
MGI:7285921	M	MP:0006380	abnormal spermatid morphology	Usp9x<tm1Tuv>/Y,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	28559472
MGI:7285921	M	MP:0001925	male infertility	Usp9x<tm1Tuv>/Y,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	28559472
MGI:7285921	M	MP:0002687	oligozoospermia	Usp9x<tm1Tuv>/Y,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	28559472
MGI:7285921	M	MP:0006379	abnormal spermatocyte morphology	Usp9x<tm1Tuv>/Y,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	28559472
MGI:7285921	M	MP:0001147	small testis	Usp9x<tm1Tuv>/Y,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	28559472
MGI:7285921	M	MP:0014052	increased male germ cell apoptosis	Usp9x<tm1Tuv>/Y,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	28559472
MGI:7285921	M	MP:0002216	abnormal seminiferous tubule morphology	Usp9x<tm1Tuv>/Y,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	28559472
MGI:7285921	M	MP:0004852	decreased testis weight	Usp9x<tm1Tuv>/Y,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	28559472
MGI:7285921	M	MP:0004182	abnormal spermiation	Usp9x<tm1Tuv>/Y,Tg(Ddx4-cre)1Dcas/0	involves: FVB	N	28559472
MGI:7286183	M	MP:0002687	oligozoospermia	Huwe1<tm1Alas>/Y,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	29259204
MGI:7286183	M	MP:0005169	abnormal male meiosis	Huwe1<tm1Alas>/Y,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	29259204
MGI:7286183	M	MP:0006378	abnormal spermatogonia morphology	Huwe1<tm1Alas>/Y,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	29259204
MGI:7286183	M	MP:0001155	arrest of spermatogenesis	Huwe1<tm1Alas>/Y,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	29259204
MGI:7286183	M	MP:0014052	increased male germ cell apoptosis	Huwe1<tm1Alas>/Y,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	29259204
MGI:7286183	M	MP:0006379	abnormal spermatocyte morphology	Huwe1<tm1Alas>/Y,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	29259204
MGI:7286183	M	MP:0002660	abnormal caput epididymis morphology	Huwe1<tm1Alas>/Y,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	29259204
MGI:7286183	M	MP:0020362	abnormal male germ cell physiology	Huwe1<tm1Alas>/Y,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	29259204
MGI:7286183	M	MP:0001925	male infertility	Huwe1<tm1Alas>/Y,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	29259204
MGI:7286183	M	MP:0004852	decreased testis weight	Huwe1<tm1Alas>/Y,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	29259204
MGI:7286183	M	MP:0013601	increased testis apoptosis	Huwe1<tm1Alas>/Y,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	29259204
MGI:7286183	M	MP:0001147	small testis	Huwe1<tm1Alas>/Y,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	29259204
MGI:7286183	M	MP:0004901	decreased male germ cell number	Huwe1<tm1Alas>/Y,Tg(Stra8-icre)1Reb/0	involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	N	29259204
MGI:7286184	M	MP:0005389	reproductive system phenotype	Huwe1<tm1Alas>/Y,Tg(Spo11-cre)1Rsw/0	involves: 129S7/SvEvBrd	Y	29259204
MGI:7286184	M	MP:0006379	abnormal spermatocyte morphology	Huwe1<tm1Alas>/Y,Tg(Spo11-cre)1Rsw/0	involves: 129S7/SvEvBrd	N	29259204
MGI:7286185	M	MP:0005389	reproductive system phenotype	Huwe1<tm1Alas>/Y,Tg(Prm-cre)58Og/0	involves: 129S4/SvJae * 129S7/SvEvBrd	Y	29259204
MGI:7286309	M	MP:0004852	decreased testis weight	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	F	MP:0004856	decreased ovary weight	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	M	MP:0002773	decreased circulating luteinizing hormone level	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	M	MP:0002687	oligozoospermia	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	M	MP:0020869	immotile sperm	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	M	MP:0002216	abnormal seminiferous tubule morphology	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	F	MP:0009017	prolonged estrus	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	F	MP:0001935	decreased litter size	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	M	MP:0001922	reduced male fertility	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	F	MP:0001129	impaired ovarian folliculogenesis	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	F	MP:0001751	increased circulating luteinizing hormone level	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	M	MP:0001155	arrest of spermatogenesis	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	M	MP:0001935	decreased litter size	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	M	MP:0004884	abnormal testis physiology	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	F	MP:0001923	reduced female fertility	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	M	MP:0001147	small testis	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	F	MP:0002636	delayed vaginal opening	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	F	MP:0003507	abnormal ovary physiology	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	M	MP:0001156	abnormal spermatogenesis	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	M	MP:0005250	decreased Sertoli cell number	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	M	MP:0008261	arrest of male meiosis	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	F	MP:0002680	decreased corpora lutea number	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	M	MP:0002675	asthenozoospermia	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286309	F	MP:0003355	decreased ovulation rate	Foxl2<tm2.1Tre>/Foxl2<tm2.1Tre>,Gnrhr<tm1.1(cre)Uboe>/Gnrhr<+>	involves: 129S1/Sv * 129X1/SvJ	N	23340250
MGI:7286374	F	MP:0011110	preweaning lethality, incomplete penetrance	Specc1l<em4Kumc>/Specc1l<+>	involves: C57BL/6J * FVB/NJ	N	34302166
MGI:7286374	F	MP:0000111	cleft palate	Specc1l<em4Kumc>/Specc1l<+>	involves: C57BL/6J * FVB/NJ	N	34302166
MGI:7286375	F	MP:0000111	cleft palate	Specc1l<em3Kumc>/Specc1l<+>	involves: C57BL/6J * FVB/NJ	N	34302166
MGI:7286375	F	MP:0011110	preweaning lethality, incomplete penetrance	Specc1l<em3Kumc>/Specc1l<+>	involves: C57BL/6J * FVB/NJ	N	34302166
MGI:7287384	F	MP:0005389	reproductive system phenotype	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad1<tm2Rob>/Smad1<tm2Rob>	involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6	Y	35383354
MGI:7287385	F	MP:0005389	reproductive system phenotype	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	Y	35383354
MGI:7287387	F	MP:0001729	impaired embryo implantation	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * 129S6/SvEvTac * C57BL/6	N	35383354
MGI:7287387	F	MP:0001926	female infertility	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * 129S6/SvEvTac * C57BL/6	N	35383354
MGI:7287387	F	MP:0009662	abnormal uterine receptivity	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * 129S6/SvEvTac * C57BL/6	N	35383354
MGI:7287387	F	MP:0008995	early reproductive senescence	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * 129S6/SvEvTac * C57BL/6	N	35383354
MGI:7287387	F	MP:0003845	abnormal decidualization	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * 129S6/SvEvTac * C57BL/6	N	35383354
MGI:7287387	F	MP:0001935	decreased litter size	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * 129S6/SvEvTac * C57BL/6	N	35383354
MGI:7287387	F	MP:0005389	reproductive system phenotype	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * 129S6/SvEvTac * C57BL/6	Y	35383354
MGI:7287387	F	MP:0001923	reduced female fertility	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * 129S6/SvEvTac * C57BL/6	N	35383354
MGI:7287387	F	MP:0001672	abnormal embryo development	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * 129S6/SvEvTac * C57BL/6	N	35383354
MGI:7287387	F	MP:0009661	abnormal pregnancy	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * 129S6/SvEvTac * C57BL/6	N	35383354
MGI:7287387	F	MP:0009649	delayed embryo implantation	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * 129S6/SvEvTac * C57BL/6	N	35383354
MGI:7287387	F	MP:0009666	abnormal embryo attachment	Ltf<tm1(icre)Tdku>/Ltf<+>,Smad1<tm2Rob>/Smad1<tm2Rob>,Smad5<tm1Huy>/Smad5<tm1Huy>	involves: 129P2/OlaHsd * 129S/SvEv * 129S6/SvEvTac * C57BL/6	N	35383354
MGI:7287416	M	MP:0011093	embryonic lethality at implantation, complete penetrance	Uba1<em1Imat>/Y	CD1-Uba1<em1Imat>	N	35440748
MGI:7287416	M	MP:0014134	abnormal embryo morphology	Uba1<em1Imat>/Y	CD1-Uba1<em1Imat>	N	35440748
MGI:7287465	M	MP:0001925	male infertility	Cntln<em1Wli>/Cntln<em1Wli>	involves: C57BL/6J * DBA/2J	N	34389728
MGI:7287500	M	MP:0005578	teratozoospermia	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0001932	abnormal spermiogenesis	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0002675	asthenozoospermia	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0031356	abnormal outer dense fiber morphology	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0009838	abnormal sperm axoneme morphology	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0001156	abnormal spermatogenesis	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0031386	elongated manchette	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0030590	abnormal sperm fibrous sheath morphology	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0006380	abnormal spermatid morphology	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0008892	abnormal sperm flagellum morphology	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0005388	respiratory system phenotype	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	Y	35587122
MGI:7287500	M	MP:0004884	abnormal testis physiology	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0002662	abnormal cauda epididymis morphology	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0009239	short sperm flagellum	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0009232	abnormal sperm nucleus morphology	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0009377	ectopic manchette	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0009242	thin sperm flagellum	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0008545	absent sperm flagellum	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0002216	abnormal seminiferous tubule morphology	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0002687	oligozoospermia	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0009238	coiled sperm flagellum	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0009230	abnormal sperm head morphology	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287500	M	MP:0001925	male infertility	Ccdc38<em1Cya>/Ccdc38<em1Cya>	C57BL/6J-Ccdc38<em1Cya>/Cya	N	35587122
MGI:7287525	M	MP:0031431	increased spongiotrophoblast cell number	Rr27<tm1Kpfe>/Rr27<+>,Tg(Tpbpa-cre,-EGFP)5Jcc/0	involves: 129S1/Sv * 129X1/SvJ	N	34982814
MGI:7287525	F	MP:0008957	abnormal placenta junctional zone morphology	Rr27<tm1Kpfe>/Rr27<+>,Tg(Tpbpa-cre,-EGFP)5Jcc/0	involves: 129S1/Sv * 129X1/SvJ	N	34982814
MGI:7287525	F	MP:0005033	abnormal trophoblast giant cell morphology	Rr27<tm1Kpfe>/Rr27<+>,Tg(Tpbpa-cre,-EGFP)5Jcc/0	involves: 129S1/Sv * 129X1/SvJ	N	34982814
MGI:7287525	M	MP:0008957	abnormal placenta junctional zone morphology	Rr27<tm1Kpfe>/Rr27<+>,Tg(Tpbpa-cre,-EGFP)5Jcc/0	involves: 129S1/Sv * 129X1/SvJ	N	34982814
MGI:7287525	F	MP:0031431	increased spongiotrophoblast cell number	Rr27<tm1Kpfe>/Rr27<+>,Tg(Tpbpa-cre,-EGFP)5Jcc/0	involves: 129S1/Sv * 129X1/SvJ	N	34982814
MGI:7287664	M	MP:0004852	decreased testis weight	Ddx5<tm1.1Arte>/Ddx5<tm1.1Arte>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6NTac * FVB	N	33666296
MGI:7287664	M	MP:0001155	arrest of spermatogenesis	Ddx5<tm1.1Arte>/Ddx5<tm1.1Arte>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6NTac * FVB	N	33666296
MGI:7287664	M	MP:0004901	decreased male germ cell number	Ddx5<tm1.1Arte>/Ddx5<tm1.1Arte>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6NTac * FVB	N	33666296
MGI:7287664	M	MP:0001925	male infertility	Ddx5<tm1.1Arte>/Ddx5<tm1.1Arte>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6NTac * FVB	N	33666296
MGI:7287664	M	MP:0002662	abnormal cauda epididymis morphology	Ddx5<tm1.1Arte>/Ddx5<tm1.1Arte>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6NTac * FVB	N	33666296
MGI:7287664	M	MP:0002216	abnormal seminiferous tubule morphology	Ddx5<tm1.1Arte>/Ddx5<tm1.1Arte>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6NTac * FVB	N	33666296
MGI:7287664	M	MP:0005159	azoospermia	Ddx5<tm1.1Arte>/Ddx5<tm1.1Arte>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6NTac * FVB	N	33666296
MGI:7287664	M	MP:0020362	abnormal male germ cell physiology	Ddx5<tm1.1Arte>/Ddx5<tm1.1Arte>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6NTac * FVB	N	33666296
MGI:7287664	M	MP:0001147	small testis	Ddx5<tm1.1Arte>/Ddx5<tm1.1Arte>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6NTac * FVB	N	33666296
MGI:7287839	M	MP:0014052	increased male germ cell apoptosis	Hnrnpk<tm1.1Cya>/Hnrnpk<tm1.1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	35455958
MGI:7287839	M	MP:0001147	small testis	Hnrnpk<tm1.1Cya>/Hnrnpk<tm1.1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	35455958
MGI:7287839	M	MP:0008261	arrest of male meiosis	Hnrnpk<tm1.1Cya>/Hnrnpk<tm1.1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	35455958
MGI:7287839	M	MP:0001265	decreased body size	Hnrnpk<tm1.1Cya>/Hnrnpk<tm1.1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	35455958
MGI:7287839	M	MP:0009248	small caput epididymis	Hnrnpk<tm1.1Cya>/Hnrnpk<tm1.1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	35455958
MGI:7287839	M	MP:0004852	decreased testis weight	Hnrnpk<tm1.1Cya>/Hnrnpk<tm1.1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	35455958
MGI:7287839	M	MP:0001925	male infertility	Hnrnpk<tm1.1Cya>/Hnrnpk<tm1.1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	35455958
MGI:7287839	M	MP:0031210	small cauda epididymis	Hnrnpk<tm1.1Cya>/Hnrnpk<tm1.1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6 * FVB/NJ	N	35455958
MGI:7287842	M	MP:0005159	azoospermia	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Tg(Ddx4-cre)1Dcas/0	involves: 129P2/OlaHsd * C57BL/6J * FVB	N	34518881
MGI:7287842	M	MP:0001147	small testis	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Tg(Ddx4-cre)1Dcas/0	involves: 129P2/OlaHsd * C57BL/6J * FVB	N	34518881
MGI:7287842	M	MP:0004806	absent germ cells	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Tg(Ddx4-cre)1Dcas/0	involves: 129P2/OlaHsd * C57BL/6J * FVB	N	34518881
MGI:7287842	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Tg(Ddx4-cre)1Dcas/0	involves: 129P2/OlaHsd * C57BL/6J * FVB	N	34518881
MGI:7287842	M	MP:0004852	decreased testis weight	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Tg(Ddx4-cre)1Dcas/0	involves: 129P2/OlaHsd * C57BL/6J * FVB	N	34518881
MGI:7287842	M	MP:0002216	abnormal seminiferous tubule morphology	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Tg(Ddx4-cre)1Dcas/0	involves: 129P2/OlaHsd * C57BL/6J * FVB	N	34518881
MGI:7287842	M	MP:0002662	abnormal cauda epididymis morphology	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Tg(Ddx4-cre)1Dcas/0	involves: 129P2/OlaHsd * C57BL/6J * FVB	N	34518881
MGI:7287844	M	MP:0009831	abnormal sperm midpiece morphology	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7287844	M	MP:0004852	decreased testis weight	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7287844	M	MP:0001147	small testis	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7287844	M	MP:0009839	multiflagellated sperm	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7287844	M	MP:0009230	abnormal sperm head morphology	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7287844	M	MP:0014052	increased male germ cell apoptosis	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7287844	M	MP:0004543	abnormal sperm physiology	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7287844	M	MP:0009237	kinked sperm flagellum	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7287844	M	MP:0001935	decreased litter size	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7287844	M	MP:0002674	abnormal sperm motility	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7287844	M	MP:0002687	oligozoospermia	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7287844	M	MP:0031427	increased sperm progressive motility	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7287844	M	MP:0005578	teratozoospermia	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7287844	M	MP:0001922	reduced male fertility	Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Ccn6<tm1(cre)Mawa>/Ccn6<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	N	34518881
MGI:7293339	M	MP:0021111	decreased social investigation	Svbp<em1Mjom>/Svbp<em1Mjom>	C57BL/6-Svbp<em1Mjom>	N	31363758
MGI:7294208	M	MP:0003674	oxidative stress	Lancl1<tm1Pfw>/Lancl1<tm1.1Pfw>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6 * FVB	N	35469022
MGI:7294208	M	MP:0002675	asthenozoospermia	Lancl1<tm1Pfw>/Lancl1<tm1.1Pfw>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6 * FVB	N	35469022
MGI:7294208	M	MP:0001156	abnormal spermatogenesis	Lancl1<tm1Pfw>/Lancl1<tm1.1Pfw>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6 * FVB	N	35469022
MGI:7294208	M	MP:0004543	abnormal sperm physiology	Lancl1<tm1Pfw>/Lancl1<tm1.1Pfw>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6 * FVB	N	35469022
MGI:7294208	M	MP:0001922	reduced male fertility	Lancl1<tm1Pfw>/Lancl1<tm1.1Pfw>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6 * FVB	N	35469022
MGI:7294208	M	MP:0002687	oligozoospermia	Lancl1<tm1Pfw>/Lancl1<tm1.1Pfw>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6 * FVB	N	35469022
MGI:7294208	M	MP:0020451	decreased sperm progressive motility	Lancl1<tm1Pfw>/Lancl1<tm1.1Pfw>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6 * FVB	N	35469022
MGI:7294208	M	MP:0004852	decreased testis weight	Lancl1<tm1Pfw>/Lancl1<tm1.1Pfw>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6 * FVB	N	35469022
MGI:7294208	M	MP:0004901	decreased male germ cell number	Lancl1<tm1Pfw>/Lancl1<tm1.1Pfw>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6 * FVB	N	35469022
MGI:7294209	M	MP:0001156	abnormal spermatogenesis	Gt(ROSA)26Sor<tm2(CAG-Lancl1)Pfw>/Gt(ROSA)26Sor<+>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6 * FVB	N	35469022
MGI:7294209	M	MP:0030603	increased sperm number	Gt(ROSA)26Sor<tm2(CAG-Lancl1)Pfw>/Gt(ROSA)26Sor<+>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6 * FVB	N	35469022
MGI:7294209	M	MP:0031426	increased sperm motility	Gt(ROSA)26Sor<tm2(CAG-Lancl1)Pfw>/Gt(ROSA)26Sor<+>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6 * FVB	N	35469022
MGI:7294209	M	MP:0003186	abnormal redox activity	Gt(ROSA)26Sor<tm2(CAG-Lancl1)Pfw>/Gt(ROSA)26Sor<+>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6 * FVB	N	35469022
MGI:7294209	M	MP:0020450	abnormal sperm progressive motility	Gt(ROSA)26Sor<tm2(CAG-Lancl1)Pfw>/Gt(ROSA)26Sor<+>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6 * FVB	N	35469022
MGI:7294209	M	MP:0008280	abnormal male germ cell apoptosis	Gt(ROSA)26Sor<tm2(CAG-Lancl1)Pfw>/Gt(ROSA)26Sor<+>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6 * FVB	N	35469022
MGI:7294209	M	MP:0008413	decreased cellular sensitivity to oxidative stress	Gt(ROSA)26Sor<tm2(CAG-Lancl1)Pfw>/Gt(ROSA)26Sor<+>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6 * FVB	N	35469022
MGI:7294354	F	MP:0005386	behavior/neurological phenotype	Dgkh<em1Mjz>/Dgkh<em1Mjz>	C57BL/6-Dgkh<em1Mjz>	Y	30985063
MGI:7294356	F	MP:0005386	behavior/neurological phenotype	Dgki<tm1Mtop>/Dgki<tm1Mtop>	B6.129-Dgki<tm1Mtop>	Y	30985063
MGI:7294356	F	MP:0001386	abnormal maternal nurturing	Dgki<tm1Mtop>/Dgki<tm1Mtop>	B6.129-Dgki<tm1Mtop>	N	30985063
MGI:7294358	F	MP:0001386	abnormal maternal nurturing	Dgkh<em1Mjz>/Dgkh<em1Mjz>,Dgki<tm1Mtop>/Dgki<tm1Mtop>	B6.Cg-Dgki<tm1Mtop> Dgkh<em1Mjz>	N	30985063
MGI:7294358	F	MP:0001399	hyperactivity	Dgkh<em1Mjz>/Dgkh<em1Mjz>,Dgki<tm1Mtop>/Dgki<tm1Mtop>	B6.Cg-Dgki<tm1Mtop> Dgkh<em1Mjz>	N	30985063
MGI:7294358	F	MP:0005386	behavior/neurological phenotype	Dgkh<em1Mjz>/Dgkh<em1Mjz>,Dgki<tm1Mtop>/Dgki<tm1Mtop>	B6.Cg-Dgki<tm1Mtop> Dgkh<em1Mjz>	Y	30985063
MGI:7294358	F	MP:0020379	abnormal sucrose solution preference	Dgkh<em1Mjz>/Dgkh<em1Mjz>,Dgki<tm1Mtop>/Dgki<tm1Mtop>	B6.Cg-Dgki<tm1Mtop> Dgkh<em1Mjz>	N	30985063
MGI:7294358	F	MP:0001501	abnormal sleep pattern	Dgkh<em1Mjz>/Dgkh<em1Mjz>,Dgki<tm1Mtop>/Dgki<tm1Mtop>	B6.Cg-Dgki<tm1Mtop> Dgkh<em1Mjz>	N	30985063
MGI:7294358	F	MP:0001384	abnormal pup retrieval	Dgkh<em1Mjz>/Dgkh<em1Mjz>,Dgki<tm1Mtop>/Dgki<tm1Mtop>	B6.Cg-Dgki<tm1Mtop> Dgkh<em1Mjz>	N	30985063
MGI:7294358	F	MP:0001363	increased anxiety-related response	Dgkh<em1Mjz>/Dgkh<em1Mjz>,Dgki<tm1Mtop>/Dgki<tm1Mtop>	B6.Cg-Dgki<tm1Mtop> Dgkh<em1Mjz>	N	30985063
MGI:7294358	F	MP:0003063	increased coping response	Dgkh<em1Mjz>/Dgkh<em1Mjz>,Dgki<tm1Mtop>/Dgki<tm1Mtop>	B6.Cg-Dgki<tm1Mtop> Dgkh<em1Mjz>	N	30985063
MGI:7294376	M	MP:0031425	enhanced male fertility	Il6<tm1Kopf>/Il6<+>,Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * 129S2/SvPas * C57BL/6	N	31664153
MGI:7294376	M	MP:0031426	increased sperm motility	Il6<tm1Kopf>/Il6<+>,Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * 129S2/SvPas * C57BL/6	N	31664153
MGI:7294376	M	MP:0014190	abnormal epididymis physiology	Il6<tm1Kopf>/Il6<+>,Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * 129S2/SvPas * C57BL/6	N	31664153
MGI:7294376	M	MP:0031427	increased sperm progressive motility	Il6<tm1Kopf>/Il6<+>,Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * 129S2/SvPas * C57BL/6	N	31664153
MGI:7294376	M	MP:0005578	teratozoospermia	Il6<tm1Kopf>/Il6<+>,Ncoa5<tm1Hxia>/Ncoa5<+>	involves: 129 * 129S2/SvPas * C57BL/6	N	31664153
MGI:7294530	M	MP:0001402	decreased locomotor activity	Hmga2<em1Sson>/Hmga2<+>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0004910	decreased seminal vesicle weight	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0002572	abnormal emotion/affect behavior	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0005578	teratozoospermia	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0008526	decreased cranium width	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0009230	abnormal sperm head morphology	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0008892	abnormal sperm flagellum morphology	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	F	MP:0001926	female infertility	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0008525	decreased cranium height	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0003550	short perineum	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0001402	decreased locomotor activity	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0014052	increased male germ cell apoptosis	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0001925	male infertility	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0004852	decreased testis weight	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0009105	penis prolapse	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0002687	oligozoospermia	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0011862	decreased cranium length	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0001447	abnormal nest building behavior	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7294531	M	MP:0004929	decreased epididymis weight	Hmga2<em1Sson>/Hmga2<em1Sson>	involves: C57BL/6N	N	34878116
MGI:7310028	M	MP:0008261	arrest of male meiosis	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	N	33724554
MGI:7310028	M	MP:0004852	decreased testis weight	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	N	33724554
MGI:7310028	M	MP:0001153	small seminiferous tubules	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	N	33724554
MGI:7310028	M	MP:0002687	oligozoospermia	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	N	33724554
MGI:7310028	F	MP:0005389	reproductive system phenotype	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	Y	33724554
MGI:7310028	M	MP:0001147	small testis	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	N	33724554
MGI:7310028	M	MP:0014052	increased male germ cell apoptosis	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	N	33724554
MGI:7310028	M	MP:0006379	abnormal spermatocyte morphology	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	N	33724554
MGI:7310028	M	MP:0005584	abnormal enzyme/coenzyme activity	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	N	33724554
MGI:7310028	M	MP:0004901	decreased male germ cell number	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	N	33724554
MGI:7310028	M	MP:0002662	abnormal cauda epididymis morphology	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	N	33724554
MGI:7310028	M	MP:0004884	abnormal testis physiology	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	N	33724554
MGI:7310028	M	MP:0001925	male infertility	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	N	33724554
MGI:7310028	M	MP:0001156	abnormal spermatogenesis	Rnf216<em1Lijd>/Rnf216<em1Lijd>	involves: C57BL/6	N	33724554
MGI:7310065	M	MP:0001922	reduced male fertility	Prss55<em1Huizh>/Prss55<em1Huizh>	Not Specified	N	33417308
MGI:7310065	M	MP:0011635	abnormal mitochondrial crista morphology	Prss55<em1Huizh>/Prss55<em1Huizh>	Not Specified	N	33417308
MGI:7310065	M	MP:0004543	abnormal sperm physiology	Prss55<em1Huizh>/Prss55<em1Huizh>	Not Specified	N	33417308
MGI:7310065	M	MP:0009838	abnormal sperm axoneme morphology	Prss55<em1Huizh>/Prss55<em1Huizh>	Not Specified	N	33417308
MGI:7310065	M	MP:0008892	abnormal sperm flagellum morphology	Prss55<em1Huizh>/Prss55<em1Huizh>	Not Specified	N	33417308
MGI:7310065	M	MP:0005578	teratozoospermia	Prss55<em1Huizh>/Prss55<em1Huizh>	Not Specified	N	33417308
MGI:7310065	M	MP:0031356	abnormal outer dense fiber morphology	Prss55<em1Huizh>/Prss55<em1Huizh>	Not Specified	N	33417308
MGI:7310065	M	MP:0020451	decreased sperm progressive motility	Prss55<em1Huizh>/Prss55<em1Huizh>	Not Specified	N	33417308
MGI:7310065	M	MP:0009238	coiled sperm flagellum	Prss55<em1Huizh>/Prss55<em1Huizh>	Not Specified	N	33417308
MGI:7310065	M	MP:0002675	asthenozoospermia	Prss55<em1Huizh>/Prss55<em1Huizh>	Not Specified	N	33417308
MGI:7310065	M	MP:0009230	abnormal sperm head morphology	Prss55<em1Huizh>/Prss55<em1Huizh>	Not Specified	N	33417308
MGI:7310065	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Prss55<em1Huizh>/Prss55<em1Huizh>	Not Specified	N	33417308
MGI:7310065	M	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport	Prss55<em1Huizh>/Prss55<em1Huizh>	Not Specified	N	33417308
MGI:7310207	M	MP:0014052	increased male germ cell apoptosis	Axdnd1<em1Ktmr>/Axdnd1<em1Ktmr>	C57BL/6N-Axdnd1<em1Ktmr>	N	35386379
MGI:7310207	M	MP:0001932	abnormal spermiogenesis	Axdnd1<em1Ktmr>/Axdnd1<em1Ktmr>	C57BL/6N-Axdnd1<em1Ktmr>	N	35386379
MGI:7310207	M	MP:0001147	small testis	Axdnd1<em1Ktmr>/Axdnd1<em1Ktmr>	C57BL/6N-Axdnd1<em1Ktmr>	N	35386379
MGI:7310207	M	MP:0002687	oligozoospermia	Axdnd1<em1Ktmr>/Axdnd1<em1Ktmr>	C57BL/6N-Axdnd1<em1Ktmr>	N	35386379
MGI:7310207	M	MP:0004852	decreased testis weight	Axdnd1<em1Ktmr>/Axdnd1<em1Ktmr>	C57BL/6N-Axdnd1<em1Ktmr>	N	35386379
MGI:7310207	M	MP:0009230	abnormal sperm head morphology	Axdnd1<em1Ktmr>/Axdnd1<em1Ktmr>	C57BL/6N-Axdnd1<em1Ktmr>	N	35386379
MGI:7310207	M	MP:0001925	male infertility	Axdnd1<em1Ktmr>/Axdnd1<em1Ktmr>	C57BL/6N-Axdnd1<em1Ktmr>	N	35386379
MGI:7310207	M	MP:0009376	abnormal manchette morphology	Axdnd1<em1Ktmr>/Axdnd1<em1Ktmr>	C57BL/6N-Axdnd1<em1Ktmr>	N	35386379
MGI:7310216	M	MP:0002687	oligozoospermia	Drc1<em1Mngx>/Drc1<em1Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310216	M	MP:0008545	absent sperm flagellum	Drc1<em1Mngx>/Drc1<em1Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310216	M	MP:0009239	short sperm flagellum	Drc1<em1Mngx>/Drc1<em1Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0009241	thick sperm flagellum	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0020869	immotile sperm	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0008892	abnormal sperm flagellum morphology	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0001932	abnormal spermiogenesis	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0002687	oligozoospermia	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0008545	absent sperm flagellum	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0009230	abnormal sperm head morphology	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0009376	abnormal manchette morphology	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0001925	male infertility	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0009239	short sperm flagellum	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0009838	abnormal sperm axoneme morphology	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0009237	kinked sperm flagellum	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0009238	coiled sperm flagellum	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310221	M	MP:0031438	abnormal sperm radial spoke morphology	Drc1<em2Mngx>/Drc1<em2Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0009230	abnormal sperm head morphology	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0009241	thick sperm flagellum	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0008545	absent sperm flagellum	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0001925	male infertility	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0009238	coiled sperm flagellum	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0020869	immotile sperm	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0008892	abnormal sperm flagellum morphology	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0002687	oligozoospermia	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0001932	abnormal spermiogenesis	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0031438	abnormal sperm radial spoke morphology	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0009376	abnormal manchette morphology	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0009239	short sperm flagellum	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0009838	abnormal sperm axoneme morphology	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310223	M	MP:0009237	kinked sperm flagellum	Drc1<em3Mngx>/Drc1<em3Mngx>	involves: C57BL/6 * ICR	N	34169321
MGI:7310235	F	MP:0000592	short tail	Hcfc1<em1Poche>/Hcfc1<+>,Rpl24<Bst>/Rpl24<+>	involves: C57BL/6J * C57BLKS/J	N	35013307
MGI:7310235	F	MP:0001265	decreased body size	Hcfc1<em1Poche>/Hcfc1<+>,Rpl24<Bst>/Rpl24<+>	involves: C57BL/6J * C57BLKS/J	N	35013307
MGI:7310235	F	MP:0000373	belly spot	Hcfc1<em1Poche>/Hcfc1<+>,Rpl24<Bst>/Rpl24<+>	involves: C57BL/6J * C57BLKS/J	N	35013307
MGI:7310235	F	MP:0010831	lethality, incomplete penetrance	Hcfc1<em1Poche>/Hcfc1<+>,Rpl24<Bst>/Rpl24<+>	involves: C57BL/6J * C57BLKS/J	N	35013307
MGI:7310236	M	MP:0010831	lethality, incomplete penetrance	Tg(CAG-Mmachc,-GFP)1Poche/0,Hcfc1<em1Poche>/Y	involves: C57BL/6J	N	35013307
MGI:7310236	M	MP:0005376	homeostasis/metabolism phenotype	Tg(CAG-Mmachc,-GFP)1Poche/0,Hcfc1<em1Poche>/Y	involves: C57BL/6J	Y	35013307
MGI:7310236	M	MP:0000428	abnormal craniofacial morphology	Tg(CAG-Mmachc,-GFP)1Poche/0,Hcfc1<em1Poche>/Y	involves: C57BL/6J	N	35013307
MGI:7310240	F	MP:0000373	belly spot	Hcfc1<em1Poche>/Hcfc1<em1Poche>	C57BL/6J-Hcfc1<em1Poche>	N	35013307
MGI:7310253	M	MP:0005389	reproductive system phenotype	Asb12<em1Mngx>/Y	involves: CD-1	Y	35280661
MGI:7310256	M	MP:0005389	reproductive system phenotype	Fam114a2<em1Qsh>/Fam114a2<em1Qsh>	Not Specified	Y	34315090
MGI:7310259	M	MP:0001922	reduced male fertility	Izumo3<tm1Osb>/Izumo3<tm1Osb>	involves: C57BL/6 * DBA/2	N	34114279
MGI:7310259	M	MP:0008898	abnormal acrosome morphology	Izumo3<tm1Osb>/Izumo3<tm1Osb>	involves: C57BL/6 * DBA/2	N	34114279
MGI:7310268	F	MP:0001928	abnormal ovulation	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	F	MP:0011129	decreased tertiary ovarian follicle number	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	M	MP:0004852	decreased testis weight	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	F	MP:0001923	reduced female fertility	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	F	MP:0001927	abnormal estrous cycle	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	F	MP:0001935	decreased litter size	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	M	MP:0005646	abnormal pituitary gland physiology	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	M	MP:0004901	decreased male germ cell number	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	F	MP:0002680	decreased corpora lutea number	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	F	MP:0001926	female infertility	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	F	MP:0004856	decreased ovary weight	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	F	MP:0009017	prolonged estrus	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	F	MP:0002682	decreased mature ovarian follicle number	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	F	MP:0005130	decreased follicle stimulating hormone level	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	F	MP:0005132	decreased luteinizing hormone level	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	F	MP:0001129	impaired ovarian folliculogenesis	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310268	M	MP:0005133	increased luteinizing hormone level	Gnrhr<tm2.1(GNRHR)Djb>/Gnrhr<tm2.1(GNRHR)Djb>	involves: 129 * C57BL/6J * FVB/N	N	34939930
MGI:7310300	M	MP:0002216	abnormal seminiferous tubule morphology	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<Gt(AJ0609)Wtsi>	B6N.129P2-Kpna6<Gt(AJ0609)Wtsi>	N	34473250
MGI:7310300	M	MP:0001262	decreased body weight	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<Gt(AJ0609)Wtsi>	B6N.129P2-Kpna6<Gt(AJ0609)Wtsi>	N	34473250
MGI:7310300	M	MP:0005389	reproductive system phenotype	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<Gt(AJ0609)Wtsi>	B6N.129P2-Kpna6<Gt(AJ0609)Wtsi>	Y	34473250
MGI:7310300	M	MP:0006379	abnormal spermatocyte morphology	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<Gt(AJ0609)Wtsi>	B6N.129P2-Kpna6<Gt(AJ0609)Wtsi>	N	34473250
MGI:7310300	M	MP:0006380	abnormal spermatid morphology	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<Gt(AJ0609)Wtsi>	B6N.129P2-Kpna6<Gt(AJ0609)Wtsi>	N	34473250
MGI:7310300	M	MP:0002687	oligozoospermia	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<Gt(AJ0609)Wtsi>	B6N.129P2-Kpna6<Gt(AJ0609)Wtsi>	N	34473250
MGI:7310300	M	MP:0001732	postnatal growth retardation	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<Gt(AJ0609)Wtsi>	B6N.129P2-Kpna6<Gt(AJ0609)Wtsi>	N	34473250
MGI:7310300	M	MP:0006428	ectopic Sertoli cells	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<Gt(AJ0609)Wtsi>	B6N.129P2-Kpna6<Gt(AJ0609)Wtsi>	N	34473250
MGI:7310300	M	MP:0001156	abnormal spermatogenesis	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<Gt(AJ0609)Wtsi>	B6N.129P2-Kpna6<Gt(AJ0609)Wtsi>	N	34473250
MGI:7310300	M	MP:0002784	abnormal Sertoli cell morphology	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<Gt(AJ0609)Wtsi>	B6N.129P2-Kpna6<Gt(AJ0609)Wtsi>	N	34473250
MGI:7310300	M	MP:0020356	abnormal Sertoli cell barrier function	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<Gt(AJ0609)Wtsi>	B6N.129P2-Kpna6<Gt(AJ0609)Wtsi>	N	34473250
MGI:7310300	M	MP:0005250	decreased Sertoli cell number	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<Gt(AJ0609)Wtsi>	B6N.129P2-Kpna6<Gt(AJ0609)Wtsi>	N	34473250
MGI:7310306	M	MP:0001925	male infertility	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0005250	decreased Sertoli cell number	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0001932	abnormal spermiogenesis	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0009230	abnormal sperm head morphology	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0014052	increased male germ cell apoptosis	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0001262	decreased body weight	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0004182	abnormal spermiation	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0002662	abnormal cauda epididymis morphology	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0001147	small testis	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0002660	abnormal caput epididymis morphology	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0020356	abnormal Sertoli cell barrier function	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0001153	small seminiferous tubules	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0002784	abnormal Sertoli cell morphology	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0004901	decreased male germ cell number	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0001732	postnatal growth retardation	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0006379	abnormal spermatocyte morphology	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0006380	abnormal spermatid morphology	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0004852	decreased testis weight	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0002216	abnormal seminiferous tubule morphology	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0002687	oligozoospermia	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0001156	abnormal spermatogenesis	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0020550	multinucleated giant male germ cells	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0002631	abnormal epididymis morphology	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310306	M	MP:0006428	ectopic Sertoli cells	Kpna6<tm1Bdr>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<tm1Bdr>	N	34473250
MGI:7310311	M	MP:0002687	oligozoospermia	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<Gt(AJ0609)Wtsi> Kpna6<tm1Bdr>	N	34473250
MGI:7310311	M	MP:0005389	reproductive system phenotype	Kpna6<Gt(AJ0609)Wtsi>/Kpna6<tm1Bdr>	B6N.Cg-Kpna6<Gt(AJ0609)Wtsi> Kpna6<tm1Bdr>	Y	34473250
MGI:7310312	M	MP:0010160	increased oligodendrocyte number	Akr1c14<tm1.1Penn>/Akr1c14<tm1.1Penn>	involves: FVB	N	34400844
MGI:7310312	F	MP:0009808	decreased oligodendrocyte number	Akr1c14<tm1.1Penn>/Akr1c14<tm1.1Penn>	involves: FVB	N	34400844
MGI:7310312	M	MP:0001409	increased stereotypic behavior	Akr1c14<tm1.1Penn>/Akr1c14<tm1.1Penn>	involves: FVB	N	34400844
MGI:7310312	F	MP:0013438	dysmyelination	Akr1c14<tm1.1Penn>/Akr1c14<tm1.1Penn>	involves: FVB	N	34400844
MGI:7310312	M	MP:0020351	decreased vocalization	Akr1c14<tm1.1Penn>/Akr1c14<tm1.1Penn>	involves: FVB	N	34400844
MGI:7310312	M	MP:0010540	long stride length	Akr1c14<tm1.1Penn>/Akr1c14<tm1.1Penn>	involves: FVB	N	34400844
MGI:7310312	M	MP:0001364	decreased anxiety-related response	Akr1c14<tm1.1Penn>/Akr1c14<tm1.1Penn>	involves: FVB	N	34400844
MGI:7310312	M	MP:0003858	enhanced coordination	Akr1c14<tm1.1Penn>/Akr1c14<tm1.1Penn>	involves: FVB	N	34400844
MGI:7310312	M	MP:0010050	hypermyelination	Akr1c14<tm1.1Penn>/Akr1c14<tm1.1Penn>	involves: FVB	N	34400844
MGI:7310312	M	MP:0002557	abnormal social/conspecific interaction behavior	Akr1c14<tm1.1Penn>/Akr1c14<tm1.1Penn>	involves: FVB	N	34400844
MGI:7310366	F	MP:0001260	increased body weight	2010003K11Rik<em1Cya>/2010003K11Rik<em1Cya>	C57BL/6-2010003K11Rik<em1Cya>/Cya	N	35093589
MGI:7311570	M	MP:0001922	reduced male fertility	Lmna<tm1.1Otin>/Lmna<tm1.1Otin>	involves: 129P2/OlaHsd * C57BL/6NTac	N	29703891
MGI:7311570	M	MP:0009105	penis prolapse	Lmna<tm1.1Otin>/Lmna<tm1.1Otin>	involves: 129P2/OlaHsd * C57BL/6NTac	N	29703891
MGI:7311570	F	MP:0001926	female infertility	Lmna<tm1.1Otin>/Lmna<tm1.1Otin>	involves: 129P2/OlaHsd * C57BL/6NTac	N	29703891
MGI:7311617	F	MP:0031239	increased atretic ovarian follicle number	Chd7<tm2c(EUCOMM)Wtsi>/Chd7<tm2c(EUCOMM)Wtsi>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	35402599
MGI:7311617	F	MP:0001923	reduced female fertility	Chd7<tm2c(EUCOMM)Wtsi>/Chd7<tm2c(EUCOMM)Wtsi>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	35402599
MGI:7311617	F	MP:0011121	decreased primordial ovarian follicle number	Chd7<tm2c(EUCOMM)Wtsi>/Chd7<tm2c(EUCOMM)Wtsi>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	35402599
MGI:7311617	F	MP:0031381	decreased secondary ovarian follicle number	Chd7<tm2c(EUCOMM)Wtsi>/Chd7<tm2c(EUCOMM)Wtsi>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	35402599
MGI:7311617	F	MP:0001127	small ovary	Chd7<tm2c(EUCOMM)Wtsi>/Chd7<tm2c(EUCOMM)Wtsi>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	35402599
MGI:7311617	F	MP:0013508	increased granulosa cell apoptosis	Chd7<tm2c(EUCOMM)Wtsi>/Chd7<tm2c(EUCOMM)Wtsi>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	35402599
MGI:7311617	F	MP:0004856	decreased ovary weight	Chd7<tm2c(EUCOMM)Wtsi>/Chd7<tm2c(EUCOMM)Wtsi>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	35402599
MGI:7311617	F	MP:0011125	decreased primary ovarian follicle number	Chd7<tm2c(EUCOMM)Wtsi>/Chd7<tm2c(EUCOMM)Wtsi>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	35402599
MGI:7311617	F	MP:0011129	decreased tertiary ovarian follicle number	Chd7<tm2c(EUCOMM)Wtsi>/Chd7<tm2c(EUCOMM)Wtsi>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	35402599
MGI:7311617	F	MP:0001129	impaired ovarian folliculogenesis	Chd7<tm2c(EUCOMM)Wtsi>/Chd7<tm2c(EUCOMM)Wtsi>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6 * C57BL/6J * C57BL/6N	N	35402599
MGI:7311626	M	MP:0002687	oligozoospermia	Adgb<tm1d(KOMP)Wtsi>/Adgb<tm1d(KOMP)Wtsi>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6N	N	35700329
MGI:7311626	F	MP:0005389	reproductive system phenotype	Adgb<tm1d(KOMP)Wtsi>/Adgb<tm1d(KOMP)Wtsi>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6N	Y	35700329
MGI:7311626	M	MP:0008892	abnormal sperm flagellum morphology	Adgb<tm1d(KOMP)Wtsi>/Adgb<tm1d(KOMP)Wtsi>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6N	N	35700329
MGI:7311626	M	MP:0009838	abnormal sperm axoneme morphology	Adgb<tm1d(KOMP)Wtsi>/Adgb<tm1d(KOMP)Wtsi>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6N	N	35700329
MGI:7311626	M	MP:0009239	short sperm flagellum	Adgb<tm1d(KOMP)Wtsi>/Adgb<tm1d(KOMP)Wtsi>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6N	N	35700329
MGI:7311626	M	MP:0009230	abnormal sperm head morphology	Adgb<tm1d(KOMP)Wtsi>/Adgb<tm1d(KOMP)Wtsi>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6N	N	35700329
MGI:7311626	M	MP:0005376	homeostasis/metabolism phenotype	Adgb<tm1d(KOMP)Wtsi>/Adgb<tm1d(KOMP)Wtsi>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6N	Y	35700329
MGI:7311626	M	MP:0001925	male infertility	Adgb<tm1d(KOMP)Wtsi>/Adgb<tm1d(KOMP)Wtsi>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6N	N	35700329
MGI:7311626	M	MP:0004852	decreased testis weight	Adgb<tm1d(KOMP)Wtsi>/Adgb<tm1d(KOMP)Wtsi>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6N	N	35700329
MGI:7311626	M	MP:0008898	abnormal acrosome morphology	Adgb<tm1d(KOMP)Wtsi>/Adgb<tm1d(KOMP)Wtsi>	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6N	N	35700329
MGI:7311694	M	MP:0006379	abnormal spermatocyte morphology	Rad51<tm1Csha>/Rad51<tm1Csha>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	35292640
MGI:7311694	M	MP:0002776	increased Sertoli cell number	Rad51<tm1Csha>/Rad51<tm1Csha>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	35292640
MGI:7311694	M	MP:0001147	small testis	Rad51<tm1Csha>/Rad51<tm1Csha>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	35292640
MGI:7311694	M	MP:0005169	abnormal male meiosis	Rad51<tm1Csha>/Rad51<tm1Csha>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	35292640
MGI:7311694	M	MP:0001156	abnormal spermatogenesis	Rad51<tm1Csha>/Rad51<tm1Csha>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	35292640
MGI:7311694	M	MP:0004901	decreased male germ cell number	Rad51<tm1Csha>/Rad51<tm1Csha>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	35292640
MGI:7311694	M	MP:0006378	abnormal spermatogonia morphology	Rad51<tm1Csha>/Rad51<tm1Csha>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	35292640
MGI:7311694	M	MP:0004852	decreased testis weight	Rad51<tm1Csha>/Rad51<tm1Csha>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	35292640
MGI:7311694	M	MP:0001925	male infertility	Rad51<tm1Csha>/Rad51<tm1Csha>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	35292640
MGI:7311694	M	MP:0002216	abnormal seminiferous tubule morphology	Rad51<tm1Csha>/Rad51<tm1Csha>,Tg(Ddx4-cre)1Dcas/0	involves: C57BL/6J * FVB	N	35292640
MGI:7311703	M	MP:0001156	abnormal spermatogenesis	Rad51<tm1Csha>/Rad51<tm1Csha>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/Sv * C57BL/6J	N	35292640
MGI:7311703	M	MP:0014052	increased male germ cell apoptosis	Rad51<tm1Csha>/Rad51<tm1Csha>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/Sv * C57BL/6J	N	35292640
MGI:7311703	M	MP:0004852	decreased testis weight	Rad51<tm1Csha>/Rad51<tm1Csha>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/Sv * C57BL/6J	N	35292640
MGI:7311703	M	MP:0005169	abnormal male meiosis	Rad51<tm1Csha>/Rad51<tm1Csha>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/Sv * C57BL/6J	N	35292640
MGI:7311703	M	MP:0004901	decreased male germ cell number	Rad51<tm1Csha>/Rad51<tm1Csha>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/Sv * C57BL/6J	N	35292640
MGI:7311703	M	MP:0006379	abnormal spermatocyte morphology	Rad51<tm1Csha>/Rad51<tm1Csha>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/Sv * C57BL/6J	N	35292640
MGI:7311703	M	MP:0010948	abnormal double-strand DNA break repair	Rad51<tm1Csha>/Rad51<tm1Csha>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/Sv * C57BL/6J	N	35292640
MGI:7311703	M	MP:0001147	small testis	Rad51<tm1Csha>/Rad51<tm1Csha>,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/Sv * C57BL/6J	N	35292640
MGI:7311763	M	MP:0008261	arrest of male meiosis	Henmt1<em2Pdz>/Henmt1<em2Pdz>	C57BL/6J-Henmt1<em2Pdz>	N	MGI:7311760
MGI:7311763	M	MP:0001925	male infertility	Henmt1<em2Pdz>/Henmt1<em2Pdz>	C57BL/6J-Henmt1<em2Pdz>	N	MGI:7311760
MGI:7311763	F	MP:0005389	reproductive system phenotype	Henmt1<em2Pdz>/Henmt1<em2Pdz>	C57BL/6J-Henmt1<em2Pdz>	Y	MGI:7311760
MGI:7311966	M	MP:0020451	decreased sperm progressive motility	Dnah1<ferf1>/Dnah1<ferf1>	C3Fe.B6-Dnah1<ferf1>	N	30734403
MGI:7311966	M	MP:0004543	abnormal sperm physiology	Dnah1<ferf1>/Dnah1<ferf1>	C3Fe.B6-Dnah1<ferf1>	N	30734403
MGI:7311966	M	MP:0013287	abnormal acrosome reaction	Dnah1<ferf1>/Dnah1<ferf1>	C3Fe.B6-Dnah1<ferf1>	N	30734403
MGI:7311966	M	MP:0001925	male infertility	Dnah1<ferf1>/Dnah1<ferf1>	C3Fe.B6-Dnah1<ferf1>	N	30734403
MGI:7311966	M	MP:0002675	asthenozoospermia	Dnah1<ferf1>/Dnah1<ferf1>	C3Fe.B6-Dnah1<ferf1>	N	30734403
MGI:7311966	M	MP:0000242	impaired fertilization	Dnah1<ferf1>/Dnah1<ferf1>	C3Fe.B6-Dnah1<ferf1>	N	30734403
MGI:7311966	M	MP:0030976	impaired sperm penetration of zona pellucida	Dnah1<ferf1>/Dnah1<ferf1>	C3Fe.B6-Dnah1<ferf1>	N	30734403
MGI:7311966	M	MP:0009647	decreased fertilization frequency	Dnah1<ferf1>/Dnah1<ferf1>	C3Fe.B6-Dnah1<ferf1>	N	30734403
MGI:7311986	F	MP:0003674	oxidative stress	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0020354	increased endoplasmic reticulum stress	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0001750	increased circulating follicle stimulating hormone level	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0002777	absent ovarian follicles	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0004231	abnormal calcium ion homeostasis	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0001134	absent corpus luteum	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0009093	oocyte degeneration	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0005376	homeostasis/metabolism phenotype	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	Y	29467381
MGI:7311986	F	MP:0031420	decreased superovulation rate	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0031020	premature ovarian failure	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0001751	increased circulating luteinizing hormone level	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0001127	small ovary	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0001126	abnormal ovary morphology	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0031381	decreased secondary ovarian follicle number	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0011121	decreased primordial ovarian follicle number	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0004856	decreased ovary weight	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0005181	decreased circulating estradiol level	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0011125	decreased primary ovarian follicle number	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0031239	increased atretic ovarian follicle number	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0001129	impaired ovarian folliculogenesis	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0001923	reduced female fertility	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0001262	decreased body weight	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0001935	decreased litter size	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7311986	F	MP:0013508	increased granulosa cell apoptosis	Tmco1<tm1Tsta>/Tmco1<tm1Tsta>	B6.Cg-Tmco1<tm1Tsta>	N	29467381
MGI:7312025	M	MP:0001156	abnormal spermatogenesis	Fbxo38<em1Crmk>/Fbxo38<em1Crmk>	C57BL/6N-Fbxo38<em1Crmk>	N	35769260
MGI:7312025	M	MP:0002687	oligozoospermia	Fbxo38<em1Crmk>/Fbxo38<em1Crmk>	C57BL/6N-Fbxo38<em1Crmk>	N	35769260
MGI:7312025	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Fbxo38<em1Crmk>/Fbxo38<em1Crmk>	C57BL/6N-Fbxo38<em1Crmk>	N	35769260
MGI:7312025	M	MP:0001922	reduced male fertility	Fbxo38<em1Crmk>/Fbxo38<em1Crmk>	C57BL/6N-Fbxo38<em1Crmk>	N	35769260
MGI:7312025	M	MP:0005169	abnormal male meiosis	Fbxo38<em1Crmk>/Fbxo38<em1Crmk>	C57BL/6N-Fbxo38<em1Crmk>	N	35769260
MGI:7312025	M	MP:0002216	abnormal seminiferous tubule morphology	Fbxo38<em1Crmk>/Fbxo38<em1Crmk>	C57BL/6N-Fbxo38<em1Crmk>	N	35769260
MGI:7312025	M	MP:0004109	abnormal Sertoli cell development	Fbxo38<em1Crmk>/Fbxo38<em1Crmk>	C57BL/6N-Fbxo38<em1Crmk>	N	35769260
MGI:7312025	M	MP:0004852	decreased testis weight	Fbxo38<em1Crmk>/Fbxo38<em1Crmk>	C57BL/6N-Fbxo38<em1Crmk>	N	35769260
MGI:7312031	M	MP:0006380	abnormal spermatid morphology	Sox30<em1Laye>/Sox30<em1Laye>	C57BL/6J-Sox30<em1Laye>	N	29866902
MGI:7312031	M	MP:0020550	multinucleated giant male germ cells	Sox30<em1Laye>/Sox30<em1Laye>	C57BL/6J-Sox30<em1Laye>	N	29866902
MGI:7312031	M	MP:0008279	arrest of spermiogenesis	Sox30<em1Laye>/Sox30<em1Laye>	C57BL/6J-Sox30<em1Laye>	N	29866902
MGI:7312031	M	MP:0002631	abnormal epididymis morphology	Sox30<em1Laye>/Sox30<em1Laye>	C57BL/6J-Sox30<em1Laye>	N	29866902
MGI:7312031	M	MP:0005159	azoospermia	Sox30<em1Laye>/Sox30<em1Laye>	C57BL/6J-Sox30<em1Laye>	N	29866902
MGI:7312031	M	MP:0001925	male infertility	Sox30<em1Laye>/Sox30<em1Laye>	C57BL/6J-Sox30<em1Laye>	N	29866902
MGI:7312031	M	MP:0004852	decreased testis weight	Sox30<em1Laye>/Sox30<em1Laye>	C57BL/6J-Sox30<em1Laye>	N	29866902
MGI:7312031	M	MP:0031355	abnormal proacrosomal vesicle fusion	Sox30<em1Laye>/Sox30<em1Laye>	C57BL/6J-Sox30<em1Laye>	N	29866902
MGI:7312031	F	MP:0005389	reproductive system phenotype	Sox30<em1Laye>/Sox30<em1Laye>	C57BL/6J-Sox30<em1Laye>	Y	29866902
MGI:7312031	M	MP:0014052	increased male germ cell apoptosis	Sox30<em1Laye>/Sox30<em1Laye>	C57BL/6J-Sox30<em1Laye>	N	29866902
MGI:7312031	M	MP:0001147	small testis	Sox30<em1Laye>/Sox30<em1Laye>	C57BL/6J-Sox30<em1Laye>	N	29866902
MGI:7312031	M	MP:0006379	abnormal spermatocyte morphology	Sox30<em1Laye>/Sox30<em1Laye>	C57BL/6J-Sox30<em1Laye>	N	29866902
MGI:7312144	M	MP:0008898	abnormal acrosome morphology	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	N	26853561
MGI:7312144	M	MP:0005159	azoospermia	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	N	26853561
MGI:7312144	M	MP:0001147	small testis	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	N	26853561
MGI:7312144	M	MP:0006380	abnormal spermatid morphology	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	N	26853561
MGI:7312144	M	MP:0009838	abnormal sperm axoneme morphology	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	N	26853561
MGI:7312144	M	MP:0002631	abnormal epididymis morphology	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	N	26853561
MGI:7312144	M	MP:0001156	abnormal spermatogenesis	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	N	26853561
MGI:7312144	M	MP:0008279	arrest of spermiogenesis	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	N	26853561
MGI:7312144	M	MP:0014052	increased male germ cell apoptosis	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	N	26853561
MGI:7312144	M	MP:0009376	abnormal manchette morphology	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	N	26853561
MGI:7312144	M	MP:0001155	arrest of spermatogenesis	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	N	26853561
MGI:7312144	M	MP:0001925	male infertility	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	N	26853561
MGI:7312144	M	MP:0020550	multinucleated giant male germ cells	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	N	26853561
MGI:7312144	F	MP:0005389	reproductive system phenotype	Rfx2<tm1Hncs>/Rfx2<tm1Hncs>	involves: 129S6/SvEvTac * C57BL/6	Y	26853561
MGI:7314168	M	MP:0031389	abnormal ectoplasmic specialization morphology	Asb17<em1Bzhg>/Asb17<em1Bzhg>	involves: CD-1	N	35070814
MGI:7314168	M	MP:0004884	abnormal testis physiology	Asb17<em1Bzhg>/Asb17<em1Bzhg>	involves: CD-1	N	35070814
MGI:7314168	M	MP:0002687	oligozoospermia	Asb17<em1Bzhg>/Asb17<em1Bzhg>	involves: CD-1	N	35070814
MGI:7314168	M	MP:0004182	abnormal spermiation	Asb17<em1Bzhg>/Asb17<em1Bzhg>	involves: CD-1	N	35070814
MGI:7314168	M	MP:0005389	reproductive system phenotype	Asb17<em1Bzhg>/Asb17<em1Bzhg>	involves: CD-1	Y	35070814
MGI:7314237	M	MP:0001156	abnormal spermatogenesis	Cry1<em1Liga>/Cry1<em1Liga>	involves: C57BL/6	N	29411926
MGI:7314237	M	MP:0005389	reproductive system phenotype	Cry1<em1Liga>/Cry1<em1Liga>	involves: C57BL/6	Y	29411926
MGI:7314237	M	MP:0014052	increased male germ cell apoptosis	Cry1<em1Liga>/Cry1<em1Liga>	involves: C57BL/6	N	29411926
MGI:7314237	M	MP:0002216	abnormal seminiferous tubule morphology	Cry1<em1Liga>/Cry1<em1Liga>	involves: C57BL/6	N	29411926
MGI:7314237	M	MP:0002687	oligozoospermia	Cry1<em1Liga>/Cry1<em1Liga>	involves: C57BL/6	N	29411926
MGI:7314237	M	MP:0005376	homeostasis/metabolism phenotype	Cry1<em1Liga>/Cry1<em1Liga>	involves: C57BL/6	Y	29411926
MGI:7314237	M	MP:0004884	abnormal testis physiology	Cry1<em1Liga>/Cry1<em1Liga>	involves: C57BL/6	N	29411926
MGI:7314398	F	MP:0001125	abnormal oocyte morphology	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J	N	30283081
MGI:7314398	F	MP:0001127	small ovary	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J	N	30283081
MGI:7314398	F	MP:0001131	abnormal ovarian follicle morphology	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J	N	30283081
MGI:7314398	F	MP:0001129	impaired ovarian folliculogenesis	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J	N	30283081
MGI:7314398	F	MP:0009648	abnormal superovulation	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J	N	30283081
MGI:7314398	F	MP:0031382	absent secondary ovarian follicles	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J	N	30283081
MGI:7314398	F	MP:0001923	reduced female fertility	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J	N	30283081
MGI:7314398	F	MP:0001134	absent corpus luteum	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J	N	30283081
MGI:7314398	F	MP:0031420	decreased superovulation rate	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J	N	30283081
MGI:7314401	F	MP:0002777	absent ovarian follicles	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0001129	impaired ovarian folliculogenesis	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0031382	absent secondary ovarian follicles	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0001134	absent corpus luteum	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0011124	increased primary ovarian follicle number	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0009648	abnormal superovulation	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0004805	absent oocytes	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0001127	small ovary	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0011121	decreased primordial ovarian follicle number	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0001131	abnormal ovarian follicle morphology	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0013272	abnormal translation	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0001125	abnormal oocyte morphology	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0001926	female infertility	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0031020	premature ovarian failure	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0031381	decreased secondary ovarian follicle number	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0005621	abnormal cell physiology	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314401	F	MP:0031422	failure of superovulation	Dcaf13<em2Hyfn>/Dcaf13<em2Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6	N	30283081
MGI:7314486	M	MP:0004543	abnormal sperm physiology	Ndufa13<em1Nju>/Ndufa13<+>	C57BL/6-Ndufa13<em1Nju>	N	35312628
MGI:7314486	M	MP:0004884	abnormal testis physiology	Ndufa13<em1Nju>/Ndufa13<+>	C57BL/6-Ndufa13<em1Nju>	N	35312628
MGI:7314486	M	MP:0001146	abnormal testis morphology	Ndufa13<em1Nju>/Ndufa13<+>	C57BL/6-Ndufa13<em1Nju>	N	35312628
MGI:7314486	M	MP:0002216	abnormal seminiferous tubule morphology	Ndufa13<em1Nju>/Ndufa13<+>	C57BL/6-Ndufa13<em1Nju>	N	35312628
MGI:7314486	M	MP:0014052	increased male germ cell apoptosis	Ndufa13<em1Nju>/Ndufa13<+>	C57BL/6-Ndufa13<em1Nju>	N	35312628
MGI:7314486	M	MP:0002780	decreased circulating testosterone level	Ndufa13<em1Nju>/Ndufa13<+>	C57BL/6-Ndufa13<em1Nju>	N	35312628
MGI:7314486	M	MP:0020451	decreased sperm progressive motility	Ndufa13<em1Nju>/Ndufa13<+>	C57BL/6-Ndufa13<em1Nju>	N	35312628
MGI:7314486	M	MP:0002675	asthenozoospermia	Ndufa13<em1Nju>/Ndufa13<+>	C57BL/6-Ndufa13<em1Nju>	N	35312628
MGI:7314486	M	MP:0003674	oxidative stress	Ndufa13<em1Nju>/Ndufa13<+>	C57BL/6-Ndufa13<em1Nju>	N	35312628
MGI:7314486	M	MP:0005389	reproductive system phenotype	Ndufa13<em1Nju>/Ndufa13<+>	C57BL/6-Ndufa13<em1Nju>	Y	35312628
MGI:7314486	M	MP:0006036	abnormal mitochondrial physiology	Ndufa13<em1Nju>/Ndufa13<+>	C57BL/6-Ndufa13<em1Nju>	N	35312628
MGI:7314486	M	MP:0002687	oligozoospermia	Ndufa13<em1Nju>/Ndufa13<+>	C57BL/6-Ndufa13<em1Nju>	N	35312628
MGI:7316446	M	MP:0009237	kinked sperm flagellum	Emc10<tm1.2Smoc>/Emc10<tm1.2Smoc>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J	N	29659949
MGI:7316446	M	MP:0009243	hairpin sperm flagellum	Emc10<tm1.2Smoc>/Emc10<tm1.2Smoc>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J	N	29659949
MGI:7316446	M	MP:0005584	abnormal enzyme/coenzyme activity	Emc10<tm1.2Smoc>/Emc10<tm1.2Smoc>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J	N	29659949
MGI:7316446	M	MP:0031393	abnormal bicarbonate homeostasis	Emc10<tm1.2Smoc>/Emc10<tm1.2Smoc>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J	N	29659949
MGI:7316446	M	MP:0000242	impaired fertilization	Emc10<tm1.2Smoc>/Emc10<tm1.2Smoc>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J	N	29659949
MGI:7316446	M	MP:0004852	decreased testis weight	Emc10<tm1.2Smoc>/Emc10<tm1.2Smoc>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J	N	29659949
MGI:7316446	M	MP:0003666	impaired sperm capacitation	Emc10<tm1.2Smoc>/Emc10<tm1.2Smoc>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J	N	29659949
MGI:7316446	M	MP:0002675	asthenozoospermia	Emc10<tm1.2Smoc>/Emc10<tm1.2Smoc>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J	N	29659949
MGI:7316446	M	MP:0004542	impaired acrosome reaction	Emc10<tm1.2Smoc>/Emc10<tm1.2Smoc>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J	N	29659949
MGI:7316446	M	MP:0001925	male infertility	Emc10<tm1.2Smoc>/Emc10<tm1.2Smoc>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J	N	29659949
MGI:7316446	M	MP:0002687	oligozoospermia	Emc10<tm1.2Smoc>/Emc10<tm1.2Smoc>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J	N	29659949
MGI:7316446	M	MP:0011977	abnormal sodium ion homeostasis	Emc10<tm1.2Smoc>/Emc10<tm1.2Smoc>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J	N	29659949
MGI:7316446	F	MP:0001923	reduced female fertility	Emc10<tm1.2Smoc>/Emc10<tm1.2Smoc>	involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J	N	29659949
MGI:7316546	M	MP:0001932	abnormal spermiogenesis	Katnal2<em1Zhlu>/Katnal2<em1Zhlu>	C57BL/6-Katnal2<em1Zhlu>	N	34096614
MGI:7316546	M	MP:0009230	abnormal sperm head morphology	Katnal2<em1Zhlu>/Katnal2<em1Zhlu>	C57BL/6-Katnal2<em1Zhlu>	N	34096614
MGI:7316546	M	MP:0002687	oligozoospermia	Katnal2<em1Zhlu>/Katnal2<em1Zhlu>	C57BL/6-Katnal2<em1Zhlu>	N	34096614
MGI:7316546	M	MP:0005578	teratozoospermia	Katnal2<em1Zhlu>/Katnal2<em1Zhlu>	C57BL/6-Katnal2<em1Zhlu>	N	34096614
MGI:7316546	M	MP:0001925	male infertility	Katnal2<em1Zhlu>/Katnal2<em1Zhlu>	C57BL/6-Katnal2<em1Zhlu>	N	34096614
MGI:7316546	M	MP:0002675	asthenozoospermia	Katnal2<em1Zhlu>/Katnal2<em1Zhlu>	C57BL/6-Katnal2<em1Zhlu>	N	34096614
MGI:7316557	M	MP:0020100	decreased susceptibility to diet-induced aortic fatty streak lesions	Apoe<tm1Unc>/Apoe<tm1Unc>,Nck1<tm1Paw>/Nck1<tm1Paw>,Nck2<tm3Paw>/Nck2<tm3Paw>,Tg(Cdh5-cre/ERT2)1Rha/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	MGI:7316552
MGI:7316557	M	MP:0001876	decreased inflammatory response	Apoe<tm1Unc>/Apoe<tm1Unc>,Nck1<tm1Paw>/Nck1<tm1Paw>,Nck2<tm3Paw>/Nck2<tm3Paw>,Tg(Cdh5-cre/ERT2)1Rha/0	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	MGI:7316552
MGI:7316619	F	MP:0003674	oxidative stress	Tm9sf5<em1Dzha>/Tm9sf5<em1Dzha>	C57BL/6-Tm9sf5<em1Dzha>	N	34635817
MGI:7316619	F	MP:0003355	decreased ovulation rate	Tm9sf5<em1Dzha>/Tm9sf5<em1Dzha>	C57BL/6-Tm9sf5<em1Dzha>	N	34635817
MGI:7316619	F	MP:0003718	maternal effect	Tm9sf5<em1Dzha>/Tm9sf5<em1Dzha>	C57BL/6-Tm9sf5<em1Dzha>	N	34635817
MGI:7316619	F	MP:0009363	abnormal tertiary ovarian follicle morphology	Tm9sf5<em1Dzha>/Tm9sf5<em1Dzha>	C57BL/6-Tm9sf5<em1Dzha>	N	34635817
MGI:7316619	F	MP:0001923	reduced female fertility	Tm9sf5<em1Dzha>/Tm9sf5<em1Dzha>	C57BL/6-Tm9sf5<em1Dzha>	N	34635817
MGI:7316619	F	MP:0001125	abnormal oocyte morphology	Tm9sf5<em1Dzha>/Tm9sf5<em1Dzha>	C57BL/6-Tm9sf5<em1Dzha>	N	34635817
MGI:7316619	F	MP:0031381	decreased secondary ovarian follicle number	Tm9sf5<em1Dzha>/Tm9sf5<em1Dzha>	C57BL/6-Tm9sf5<em1Dzha>	N	34635817
MGI:7316619	F	MP:0030941	enhanced autophagy	Tm9sf5<em1Dzha>/Tm9sf5<em1Dzha>	C57BL/6-Tm9sf5<em1Dzha>	N	34635817
MGI:7316619	F	MP:0008871	abnormal ovarian follicle number	Tm9sf5<em1Dzha>/Tm9sf5<em1Dzha>	C57BL/6-Tm9sf5<em1Dzha>	N	34635817
MGI:7316619	F	MP:0006036	abnormal mitochondrial physiology	Tm9sf5<em1Dzha>/Tm9sf5<em1Dzha>	C57BL/6-Tm9sf5<em1Dzha>	N	34635817
MGI:7316619	F	MP:0004024	aneuploidy	Tm9sf5<em1Dzha>/Tm9sf5<em1Dzha>	C57BL/6-Tm9sf5<em1Dzha>	N	34635817
MGI:7316619	F	MP:0011121	decreased primordial ovarian follicle number	Tm9sf5<em1Dzha>/Tm9sf5<em1Dzha>	C57BL/6-Tm9sf5<em1Dzha>	N	34635817
MGI:7316619	F	MP:0011129	decreased tertiary ovarian follicle number	Tm9sf5<em1Dzha>/Tm9sf5<em1Dzha>	C57BL/6-Tm9sf5<em1Dzha>	N	34635817
MGI:7316742	M	MP:0020550	multinucleated giant male germ cells	Tcfl5<tm1.1Frem>/Tcfl5<tm1.1Frem>	involves: C57BL/6 * CBA	N	35768632
MGI:7316742	M	MP:0001155	arrest of spermatogenesis	Tcfl5<tm1.1Frem>/Tcfl5<tm1.1Frem>	involves: C57BL/6 * CBA	N	35768632
MGI:7316742	M	MP:0002216	abnormal seminiferous tubule morphology	Tcfl5<tm1.1Frem>/Tcfl5<tm1.1Frem>	involves: C57BL/6 * CBA	N	35768632
MGI:7316742	M	MP:0008966	abnormal chiasmata formation	Tcfl5<tm1.1Frem>/Tcfl5<tm1.1Frem>	involves: C57BL/6 * CBA	N	35768632
MGI:7316742	M	MP:0014052	increased male germ cell apoptosis	Tcfl5<tm1.1Frem>/Tcfl5<tm1.1Frem>	involves: C57BL/6 * CBA	N	35768632
MGI:7316742	M	MP:0004852	decreased testis weight	Tcfl5<tm1.1Frem>/Tcfl5<tm1.1Frem>	involves: C57BL/6 * CBA	N	35768632
MGI:7316742	M	MP:0001147	small testis	Tcfl5<tm1.1Frem>/Tcfl5<tm1.1Frem>	involves: C57BL/6 * CBA	N	35768632
MGI:7316742	M	MP:0005159	azoospermia	Tcfl5<tm1.1Frem>/Tcfl5<tm1.1Frem>	involves: C57BL/6 * CBA	N	35768632
MGI:7316742	M	MP:0008261	arrest of male meiosis	Tcfl5<tm1.1Frem>/Tcfl5<tm1.1Frem>	involves: C57BL/6 * CBA	N	35768632
MGI:7316742	M	MP:0001925	male infertility	Tcfl5<tm1.1Frem>/Tcfl5<tm1.1Frem>	involves: C57BL/6 * CBA	N	35768632
MGI:7316743	M	MP:0001922	reduced male fertility	Tcfl5<tm1.1Frem>/Tcfl5<+>	involves: C57BL/6 * CBA	N	35768632
MGI:7316743	M	MP:0001935	decreased litter size	Tcfl5<tm1.1Frem>/Tcfl5<+>	involves: C57BL/6 * CBA	N	35768632
MGI:7316744	M	MP:0005159	azoospermia	Tcfl5<tm1Frem>/Tcfl5<tm1Frem>,Tg(CAG-cre/Esr1*)5Amc/0	involves: C57BL/6 * CBA	N	35768632
MGI:7316744	M	MP:0001932	abnormal spermiogenesis	Tcfl5<tm1Frem>/Tcfl5<tm1Frem>,Tg(CAG-cre/Esr1*)5Amc/0	involves: C57BL/6 * CBA	N	35768632
MGI:7316744	M	MP:0001147	small testis	Tcfl5<tm1Frem>/Tcfl5<tm1Frem>,Tg(CAG-cre/Esr1*)5Amc/0	involves: C57BL/6 * CBA	N	35768632
MGI:7316744	M	MP:0004852	decreased testis weight	Tcfl5<tm1Frem>/Tcfl5<tm1Frem>,Tg(CAG-cre/Esr1*)5Amc/0	involves: C57BL/6 * CBA	N	35768632
MGI:7316744	M	MP:0001925	male infertility	Tcfl5<tm1Frem>/Tcfl5<tm1Frem>,Tg(CAG-cre/Esr1*)5Amc/0	involves: C57BL/6 * CBA	N	35768632
MGI:7316744	M	MP:0002216	abnormal seminiferous tubule morphology	Tcfl5<tm1Frem>/Tcfl5<tm1Frem>,Tg(CAG-cre/Esr1*)5Amc/0	involves: C57BL/6 * CBA	N	35768632
MGI:7316744	M	MP:0008261	arrest of male meiosis	Tcfl5<tm1Frem>/Tcfl5<tm1Frem>,Tg(CAG-cre/Esr1*)5Amc/0	involves: C57BL/6 * CBA	N	35768632
MGI:7316744	M	MP:0020550	multinucleated giant male germ cells	Tcfl5<tm1Frem>/Tcfl5<tm1Frem>,Tg(CAG-cre/Esr1*)5Amc/0	involves: C57BL/6 * CBA	N	35768632
MGI:7316744	M	MP:0006380	abnormal spermatid morphology	Tcfl5<tm1Frem>/Tcfl5<tm1Frem>,Tg(CAG-cre/Esr1*)5Amc/0	involves: C57BL/6 * CBA	N	35768632
MGI:7316948	F	MP:0005635	decreased circulating bilirubin level	1700030J22Rik<em1(IMPC)J>/1700030J22Rik<em1(IMPC)J>	C57BL/6NJ-1700030J22Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316948	M	MP:0010506	prolonged RR interval	1700030J22Rik<em1(IMPC)J>/1700030J22Rik<em1(IMPC)J>	C57BL/6NJ-1700030J22Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316948	F	MP:0005559	increased circulating glucose level	1700030J22Rik<em1(IMPC)J>/1700030J22Rik<em1(IMPC)J>	C57BL/6NJ-1700030J22Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316950	M	MP:0005562	decreased mean corpuscular hemoglobin	Agfg2<em1(IMPC)J>/Agfg2<em1(IMPC)J>	C57BL/6NJ-Agfg2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316951	M	MP:0001304	cataract	Alas1<em1(IMPC)Mbp>/Alas1<+>	C57BL/6N-Alas1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7316951	F	MP:0004832	enlarged ovary	Alas1<em1(IMPC)Mbp>/Alas1<+>	C57BL/6N-Alas1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7316951	F	MP:0001126	abnormal ovary morphology	Alas1<em1(IMPC)Mbp>/Alas1<+>	C57BL/6N-Alas1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7316952	M	MP:0003179	thrombocytopenia	Ankrd44<em1(IMPC)J>/Ankrd44<em1(IMPC)J>	C57BL/6NJ-Ankrd44<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316952	M	MP:0011496	abnormal head size	Ankrd44<em1(IMPC)J>/Ankrd44<em1(IMPC)J>	C57BL/6NJ-Ankrd44<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316953	M	MP:0005278	abnormal cholesterol homeostasis	Arhgap20<em1(IMPC)J>/Arhgap20<em1(IMPC)J>	C57BL/6NJ-Arhgap20<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316955	M	MP:0005344	increased circulating bilirubin level	Asb18<em1(IMPC)J>/Asb18<em1(IMPC)J>	C57BL/6NJ-Asb18<em1(IMPC)J>/J	N	MGI:5576271
MGI:7316956	F	MP:0000208	decreased hematocrit	Atp11c<em1(IMPC)J>/Atp11c<em1(IMPC)J>	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316956	F	MP:0001556	increased circulating HDL cholesterol level	Atp11c<em1(IMPC)J>/Atp11c<em1(IMPC)J>	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316956	F	MP:0005278	abnormal cholesterol homeostasis	Atp11c<em1(IMPC)J>/Atp11c<em1(IMPC)J>	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316956	F	MP:0002968	increased circulating alkaline phosphatase level	Atp11c<em1(IMPC)J>/Atp11c<em1(IMPC)J>	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316956	F	MP:0000221	decreased leukocyte cell number	Atp11c<em1(IMPC)J>/Atp11c<em1(IMPC)J>	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316956	F	MP:0005344	increased circulating bilirubin level	Atp11c<em1(IMPC)J>/Atp11c<em1(IMPC)J>	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316956	F	MP:0005178	increased circulating cholesterol level	Atp11c<em1(IMPC)J>/Atp11c<em1(IMPC)J>	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316956	F	MP:0002875	decreased erythrocyte cell number	Atp11c<em1(IMPC)J>/Atp11c<em1(IMPC)J>	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316956	F	MP:0002874	decreased hemoglobin content	Atp11c<em1(IMPC)J>/Atp11c<em1(IMPC)J>	C57BL/6NJ-Atp11c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316957	F	MP:0002941	increased circulating alanine transaminase level	Atp13a3<em1(IMPC)J>/Atp13a3<em1(IMPC)J>	C57BL/6NJ-Atp13a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316957	F	MP:0005278	abnormal cholesterol homeostasis	Atp13a3<em1(IMPC)J>/Atp13a3<em1(IMPC)J>	C57BL/6NJ-Atp13a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316957	M	MP:0002644	decreased circulating triglyceride level	Atp13a3<em1(IMPC)J>/Atp13a3<em1(IMPC)J>	C57BL/6NJ-Atp13a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316957	F	MP:0011239	abnormal skin coloration	Atp13a3<em1(IMPC)J>/Atp13a3<em1(IMPC)J>	C57BL/6NJ-Atp13a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316957	F	MP:0001417	decreased exploration in new environment	Atp13a3<em1(IMPC)J>/Atp13a3<em1(IMPC)J>	C57BL/6NJ-Atp13a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316957	M	MP:0010123	increased bone mineral content	Atp13a3<em1(IMPC)J>/Atp13a3<em1(IMPC)J>	C57BL/6NJ-Atp13a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316957	M	MP:0001925	male infertility	Atp13a3<em1(IMPC)J>/Atp13a3<em1(IMPC)J>	C57BL/6NJ-Atp13a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316957	M	MP:0001488	increased startle reflex	Atp13a3<em1(IMPC)J>/Atp13a3<em1(IMPC)J>	C57BL/6NJ-Atp13a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316957	M	MP:0005562	decreased mean corpuscular hemoglobin	Atp13a3<em1(IMPC)J>/Atp13a3<em1(IMPC)J>	C57BL/6NJ-Atp13a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316957	F	MP:0010097	abnormal retina blood vessel morphology	Atp13a3<em1(IMPC)J>/Atp13a3<em1(IMPC)J>	C57BL/6NJ-Atp13a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316959	M	MP:0000208	decreased hematocrit	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316959	M	MP:0001289	persistence of hyaloid vascular system	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316959	M	MP:0001303	abnormal lens morphology	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316959	M	MP:0001258	decreased body length	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316959	M	MP:0001304	cataract	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316959	M	MP:0002100	abnormal tooth morphology	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316959	M	MP:0005344	increased circulating bilirubin level	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316959	M	MP:0005179	decreased circulating cholesterol level	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316959	M	MP:0002599	increased mean platelet volume	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316959	M	MP:0010053	decreased grip strength	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316959	M	MP:0030610	absent teeth	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316959	M	MP:0000186	decreased circulating HDL cholesterol level	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316959	M	MP:0000443	abnormal snout morphology	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316959	M	MP:0002968	increased circulating alkaline phosphatase level	Bcorl1<em1(IMPC)Tcp>/Y	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316960	F	MP:0002792	abnormal retina vasculature morphology	Bcorl1<em1(IMPC)Tcp>/Bcorl1<em1(IMPC)Tcp>	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316960	F	MP:0005179	decreased circulating cholesterol level	Bcorl1<em1(IMPC)Tcp>/Bcorl1<em1(IMPC)Tcp>	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316960	F	MP:0005561	increased mean corpuscular hemoglobin	Bcorl1<em1(IMPC)Tcp>/Bcorl1<em1(IMPC)Tcp>	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316960	F	MP:0010053	decreased grip strength	Bcorl1<em1(IMPC)Tcp>/Bcorl1<em1(IMPC)Tcp>	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316960	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Bcorl1<em1(IMPC)Tcp>/Bcorl1<em1(IMPC)Tcp>	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316960	F	MP:0001304	cataract	Bcorl1<em1(IMPC)Tcp>/Bcorl1<em1(IMPC)Tcp>	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316960	F	MP:0009142	decreased prepulse inhibition	Bcorl1<em1(IMPC)Tcp>/Bcorl1<em1(IMPC)Tcp>	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316960	F	MP:0001303	abnormal lens morphology	Bcorl1<em1(IMPC)Tcp>/Bcorl1<em1(IMPC)Tcp>	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316960	F	MP:0000063	decreased bone mineral density	Bcorl1<em1(IMPC)Tcp>/Bcorl1<em1(IMPC)Tcp>	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316960	F	MP:0000443	abnormal snout morphology	Bcorl1<em1(IMPC)Tcp>/Bcorl1<em1(IMPC)Tcp>	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316960	F	MP:0010097	abnormal retina blood vessel morphology	Bcorl1<em1(IMPC)Tcp>/Bcorl1<em1(IMPC)Tcp>	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316960	F	MP:0002599	increased mean platelet volume	Bcorl1<em1(IMPC)Tcp>/Bcorl1<em1(IMPC)Tcp>	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316960	F	MP:0010124	decreased bone mineral content	Bcorl1<em1(IMPC)Tcp>/Bcorl1<em1(IMPC)Tcp>	C57BL/6N-Bcorl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7316961	F	MP:0001914	hemorrhage	Bicra<em1(IMPC)J>/Bicra<em1(IMPC)J>	C57BL/6NJ-Bicra<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316962	F	MP:0001402	decreased locomotor activity	Brd3<em1(IMPC)J>/Brd3<em1(IMPC)J>	C57BL/6NJ-Brd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316962	M	MP:0010506	prolonged RR interval	Brd3<em1(IMPC)J>/Brd3<em1(IMPC)J>	C57BL/6NJ-Brd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316962	F	MP:0020870	decreased thigmotaxis	Brd3<em1(IMPC)J>/Brd3<em1(IMPC)J>	C57BL/6NJ-Brd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316962	F	MP:0010052	increased grip strength	Brd3<em1(IMPC)J>/Brd3<em1(IMPC)J>	C57BL/6NJ-Brd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316962	M	MP:0002075	abnormal coat/hair pigmentation	Brd3<em1(IMPC)J>/Brd3<em1(IMPC)J>	C57BL/6NJ-Brd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316962	F	MP:0004924	abnormal behavior	Brd3<em1(IMPC)J>/Brd3<em1(IMPC)J>	C57BL/6NJ-Brd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316963	M	MP:0000195	decreased circulating calcium level	C2cd2<em1(IMPC)J>/C2cd2<em1(IMPC)J>	C57BL/6NJ-C2cd2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316965	M	MP:0001925	male infertility	Ccdc40<em1(IMPC)J>/Ccdc40<em1(IMPC)J>	C57BL/6NJ-Ccdc40<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316965	M	MP:0000218	increased leukocyte cell number	Ccdc40<em1(IMPC)J>/Ccdc40<em1(IMPC)J>	C57BL/6NJ-Ccdc40<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316965	M	MP:0002941	increased circulating alanine transaminase level	Ccdc40<em1(IMPC)J>/Ccdc40<em1(IMPC)J>	C57BL/6NJ-Ccdc40<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316966	M	MP:0000218	increased leukocyte cell number	Ccnt1<em1(IMPC)J>/Ccnt1<+>	C57BL/6NJ-Ccnt1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316967	M	MP:0001488	increased startle reflex	Cdkn2aip<em1(IMPC)J>/Cdkn2aip<+>	C57BL/6NJ-Cdkn2aip<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316968	M	MP:0001925	male infertility	Cep126<tm1b(KOMP)Mbp>/Cep126<tm1b(KOMP)Mbp>	C57BL/6N-Cep126<tm1b(KOMP)Mbp>/J	N	MGI:5576271
MGI:7316969	M	MP:0005633	increased circulating sodium level	Cep295nl<tm1.1(KOMP)Vlcg>/Cep295nl<tm1.1(KOMP)Vlcg>	B6N(Cg)-Cep295nl<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:7316970	F	MP:0005278	abnormal cholesterol homeostasis	Ces3b<em1(IMPC)J>/Ces3b<em1(IMPC)J>	C57BL/6NJ-Ces3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316972	M	MP:0002644	decreased circulating triglyceride level	Cldn23<em1(IMPC)J>/Cldn23<em1(IMPC)J>	C57BL/6NJ-Cldn23<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316974	F	MP:0001417	decreased exploration in new environment	Cox7a2l<em1(IMPC)J>/Cox7a2l<+>	C57BL/6NJ-Cox7a2l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316975	F	MP:0001417	decreased exploration in new environment	Cox7a2l<em1(IMPC)J>/Cox7a2l<em1(IMPC)J>	C57BL/6NJ-Cox7a2l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316975	M	MP:0010506	prolonged RR interval	Cox7a2l<em1(IMPC)J>/Cox7a2l<em1(IMPC)J>	C57BL/6NJ-Cox7a2l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316976	M	MP:0001417	decreased exploration in new environment	Ctbp2<em1(IMPC)Bay>/Ctbp2<+>	C57BL/6N-Ctbp2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7316978	F	MP:0003795	abnormal bone structure	Dbx2<em1(IMPC)Bay>/Dbx2<em1(IMPC)Bay>	C57BL/6N-Dbx2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7316979	M	MP:0010025	decreased total body fat amount	Dclk2<em1(IMPC)J>/Dclk2<em1(IMPC)J>	C57BL/6NJ-Dclk2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316979	M	MP:0003960	increased lean body mass	Dclk2<em1(IMPC)J>/Dclk2<em1(IMPC)J>	C57BL/6NJ-Dclk2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316980	F	MP:0000538	abnormal urinary bladder morphology	Ddb1<em1(IMPC)Ccpcz>/Ddb1<+>	C57BL/6N-Ddb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7316980	F	MP:0000703	abnormal thymus morphology	Ddb1<em1(IMPC)Ccpcz>/Ddb1<+>	C57BL/6N-Ddb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7316980	M	MP:0001399	hyperactivity	Ddb1<em1(IMPC)Ccpcz>/Ddb1<+>	C57BL/6N-Ddb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7316980	F	MP:0011874	enlarged urinary bladder	Ddb1<em1(IMPC)Ccpcz>/Ddb1<+>	C57BL/6N-Ddb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7316980	F	MP:0000709	enlarged thymus	Ddb1<em1(IMPC)Ccpcz>/Ddb1<+>	C57BL/6N-Ddb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7316983	M	MP:0001552	increased circulating triglyceride level	Dnajc2<em1(IMPC)J>/Dnajc2<+>	C57BL/6NJ-Dnajc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316983	F	MP:0000218	increased leukocyte cell number	Dnajc2<em1(IMPC)J>/Dnajc2<+>	C57BL/6NJ-Dnajc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316983	M	MP:0000195	decreased circulating calcium level	Dnajc2<em1(IMPC)J>/Dnajc2<+>	C57BL/6NJ-Dnajc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316984	M	MP:0001284	absent vibrissae	Dok6<em1(IMPC)J>/Dok6<em1(IMPC)J>	C57BL/6NJ-Dok6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316985	M	MP:0001925	male infertility	Dync1li2<em1(IMPC)J>/Dync1li2<em1(IMPC)J>	C57BL/6NJ-Dync1li2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316986	M	MP:0001556	increased circulating HDL cholesterol level	E130308A19Rik<em1(IMPC)J>/E130308A19Rik<em1(IMPC)J>	C57BL/6NJ-E130308A19Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316986	M	MP:0005178	increased circulating cholesterol level	E130308A19Rik<em1(IMPC)J>/E130308A19Rik<em1(IMPC)J>	C57BL/6NJ-E130308A19Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316988	F	MP:0002590	increased mean corpuscular volume	Fam193a<em1(IMPC)J>/Fam193a<+>	C57BL/6NJ-Fam193a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316989	M	MP:0012121	sclerocornea	Fancf<em1(IMPC)J>/Fancf<em1(IMPC)J>	C57BL/6NJ-Fancf<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316989	M	MP:0005542	cornea vascularization	Fancf<em1(IMPC)J>/Fancf<em1(IMPC)J>	C57BL/6NJ-Fancf<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316989	M	MP:0001314	cornea opacity	Fancf<em1(IMPC)J>/Fancf<em1(IMPC)J>	C57BL/6NJ-Fancf<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316989	F	MP:0002590	increased mean corpuscular volume	Fancf<em1(IMPC)J>/Fancf<em1(IMPC)J>	C57BL/6NJ-Fancf<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316991	M	MP:0001146	abnormal testis morphology	Gabra5<em1(IMPC)Ccpcz>/Gabra5<em1(IMPC)Ccpcz>	C57BL/6N-Gabra5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7316991	M	MP:0000274	enlarged heart	Gabra5<em1(IMPC)Ccpcz>/Gabra5<em1(IMPC)Ccpcz>	C57BL/6N-Gabra5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7316991	M	MP:0000692	small spleen	Gabra5<em1(IMPC)Ccpcz>/Gabra5<em1(IMPC)Ccpcz>	C57BL/6N-Gabra5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7316991	M	MP:0000689	abnormal spleen morphology	Gabra5<em1(IMPC)Ccpcz>/Gabra5<em1(IMPC)Ccpcz>	C57BL/6N-Gabra5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7316991	F	MP:0000703	abnormal thymus morphology	Gabra5<em1(IMPC)Ccpcz>/Gabra5<em1(IMPC)Ccpcz>	C57BL/6N-Gabra5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7316991	M	MP:0000266	abnormal heart morphology	Gabra5<em1(IMPC)Ccpcz>/Gabra5<em1(IMPC)Ccpcz>	C57BL/6N-Gabra5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7316991	M	MP:0001147	small testis	Gabra5<em1(IMPC)Ccpcz>/Gabra5<em1(IMPC)Ccpcz>	C57BL/6N-Gabra5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7316991	F	MP:0000709	enlarged thymus	Gabra5<em1(IMPC)Ccpcz>/Gabra5<em1(IMPC)Ccpcz>	C57BL/6N-Gabra5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7316992	M	MP:0001404	no spontaneous movement	Gid8<em1(IMPC)J>/Gid8<em1(IMPC)J>	C57BL/6NJ-Gid8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7316993	M	MP:0001258	decreased body length	Glb1l3<em1(IMPC)Bay>/Glb1l3<em1(IMPC)Bay>	C57BL/6N-Glb1l3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7316993	F	MP:0003795	abnormal bone structure	Glb1l3<em1(IMPC)Bay>/Glb1l3<em1(IMPC)Bay>	C57BL/6N-Glb1l3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7316994	F	MP:0002968	increased circulating alkaline phosphatase level	Glrx3<tm1.1(KOMP)Vlcg>/Glrx3<+>	C57BL/6N-Glrx3<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:7316995	M	MP:0002626	increased heart rate	Golga4<em1(IMPC)Bay>/Golga4<+>	C57BL/6N-Golga4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7316996	F	MP:0002941	increased circulating alanine transaminase level	Gpr84<tm1.1(KOMP)Vlcg>/Gpr84<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpr84<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7316998	M	MP:0000218	increased leukocyte cell number	Gtsf1l<em1(IMPC)J>/Gtsf1l<em1(IMPC)J>	C57BL/6NJ-Gtsf1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317001	F	MP:0000195	decreased circulating calcium level	Hlcs<em1(IMPC)J>/Hlcs<+>	C57BL/6NJ-Hlcs<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317001	M	MP:0001392	abnormal locomotor behavior	Hlcs<em1(IMPC)J>/Hlcs<+>	C57BL/6NJ-Hlcs<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317001	F	MP:0000198	decreased circulating phosphate level	Hlcs<em1(IMPC)J>/Hlcs<+>	C57BL/6NJ-Hlcs<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317002	M	MP:0001200	thick skin	Hmbox1<em1(IMPC)Tcp>/Hmbox1<em1(IMPC)Tcp>	C57BL/6N-Hmbox1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7317002	M	MP:0005344	increased circulating bilirubin level	Hmbox1<em1(IMPC)Tcp>/Hmbox1<em1(IMPC)Tcp>	C57BL/6N-Hmbox1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7317002	M	MP:0003020	decreased circulating chloride level	Hmbox1<em1(IMPC)Tcp>/Hmbox1<em1(IMPC)Tcp>	C57BL/6N-Hmbox1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7317002	M	MP:0003068	enlarged kidney	Hmbox1<em1(IMPC)Tcp>/Hmbox1<em1(IMPC)Tcp>	C57BL/6N-Hmbox1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7317002	M	MP:0000702	enlarged lymph nodes	Hmbox1<em1(IMPC)Tcp>/Hmbox1<em1(IMPC)Tcp>	C57BL/6N-Hmbox1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7317002	M	MP:0009454	impaired contextual conditioning behavior	Hmbox1<em1(IMPC)Tcp>/Hmbox1<em1(IMPC)Tcp>	C57BL/6N-Hmbox1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7317002	M	MP:0000745	tremors	Hmbox1<em1(IMPC)Tcp>/Hmbox1<em1(IMPC)Tcp>	C57BL/6N-Hmbox1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7317002	M	MP:0005016	decreased lymphocyte cell number	Hmbox1<em1(IMPC)Tcp>/Hmbox1<em1(IMPC)Tcp>	C57BL/6N-Hmbox1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7317002	M	MP:0005562	decreased mean corpuscular hemoglobin	Hmbox1<em1(IMPC)Tcp>/Hmbox1<em1(IMPC)Tcp>	C57BL/6N-Hmbox1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7317002	M	MP:0000157	abnormal sternum morphology	Hmbox1<em1(IMPC)Tcp>/Hmbox1<em1(IMPC)Tcp>	C57BL/6N-Hmbox1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7317003	F	MP:0002941	increased circulating alanine transaminase level	Hmgcs1<em1(IMPC)J>/Hmgcs1<+>	C57BL/6NJ-Hmgcs1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317004	M	MP:0000274	enlarged heart	Hpdl<em1(IMPC)Mbp>/Hpdl<+>	C57BL/6N-Hpdl<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317004	F	MP:0002060	abnormal skin morphology	Hpdl<em1(IMPC)Mbp>/Hpdl<+>	C57BL/6N-Hpdl<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317004	F	MP:0002792	abnormal retina vasculature morphology	Hpdl<em1(IMPC)Mbp>/Hpdl<+>	C57BL/6N-Hpdl<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317004	F	MP:0010097	abnormal retina blood vessel morphology	Hpdl<em1(IMPC)Mbp>/Hpdl<+>	C57BL/6N-Hpdl<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317004	M	MP:0020870	decreased thigmotaxis	Hpdl<em1(IMPC)Mbp>/Hpdl<+>	C57BL/6N-Hpdl<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317004	M	MP:0004924	abnormal behavior	Hpdl<em1(IMPC)Mbp>/Hpdl<+>	C57BL/6N-Hpdl<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317004	F	MP:0001325	abnormal retina morphology	Hpdl<em1(IMPC)Mbp>/Hpdl<+>	C57BL/6N-Hpdl<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317004	M	MP:0000266	abnormal heart morphology	Hpdl<em1(IMPC)Mbp>/Hpdl<+>	C57BL/6N-Hpdl<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317004	M	MP:0001364	decreased anxiety-related response	Hpdl<em1(IMPC)Mbp>/Hpdl<+>	C57BL/6N-Hpdl<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317006	F	MP:0001402	decreased locomotor activity	Ier5l<em1(IMPC)J>/Ier5l<em1(IMPC)J>	C57BL/6NJ-Ier5l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317006	F	MP:0001399	hyperactivity	Ier5l<em1(IMPC)J>/Ier5l<em1(IMPC)J>	C57BL/6NJ-Ier5l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317006	F	MP:0003795	abnormal bone structure	Ier5l<em1(IMPC)J>/Ier5l<em1(IMPC)J>	C57BL/6NJ-Ier5l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317006	F	MP:0010124	decreased bone mineral content	Ier5l<em1(IMPC)J>/Ier5l<em1(IMPC)J>	C57BL/6NJ-Ier5l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317006	F	MP:0010097	abnormal retina blood vessel morphology	Ier5l<em1(IMPC)J>/Ier5l<em1(IMPC)J>	C57BL/6NJ-Ier5l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317006	M	MP:0001566	increased circulating phosphate level	Ier5l<em1(IMPC)J>/Ier5l<em1(IMPC)J>	C57BL/6NJ-Ier5l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317006	M	MP:0002833	increased heart weight	Ier5l<em1(IMPC)J>/Ier5l<em1(IMPC)J>	C57BL/6NJ-Ier5l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317009	F	MP:0010053	decreased grip strength	Kcnk16<em1(IMPC)J>/Kcnk16<em1(IMPC)J>	C57BL/6NJ-Kcnk16<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317011	F	MP:0002968	increased circulating alkaline phosphatase level	Klc3<em1(IMPC)J>/Klc3<em1(IMPC)J>	C57BL/6N-Klc3<em1(IMPC)J>/J	N	MGI:5576271
MGI:7317012	M	MP:0002590	increased mean corpuscular volume	Klhl2<em1(IMPC)J>/Klhl2<em1(IMPC)J>	C57BL/6NJ-Klhl2<em1(IMPC)J>/J	N	MGI:5576271
MGI:7317013	F	MP:0013279	increased fasting circulating glucose level	Lamp5<em1(IMPC)J>/Lamp5<em1(IMPC)J>	C57BL/6NJ-Lamp5<em1(IMPC)J>/J	N	MGI:5576271
MGI:7317013	F	MP:0005419	decreased circulating serum albumin level	Lamp5<em1(IMPC)J>/Lamp5<em1(IMPC)J>	C57BL/6NJ-Lamp5<em1(IMPC)J>/J	N	MGI:5576271
MGI:7317014	M	MP:0011965	decreased total retina thickness	Lct<tm1b(KOMP)Wtsi>/Lct<tm1b(KOMP)Wtsi>	C57BL/6N-Lct<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:7317014	M	MP:0001325	abnormal retina morphology	Lct<tm1b(KOMP)Wtsi>/Lct<tm1b(KOMP)Wtsi>	C57BL/6N-Lct<tm1b(KOMP)Wtsi>/Ieg	N	MGI:5576271
MGI:7317015	M	MP:0002590	increased mean corpuscular volume	Lin52<em1(IMPC)J>/Lin52<+>	C57BL/6NJ-Lin52<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317016	M	MP:0001417	decreased exploration in new environment	Mapk11<tm1b(EUCOMM)Hmgu>/Mapk11<tm1b(EUCOMM)Hmgu>	C57BL/6N-Mapk11<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:7317017	M	MP:0005562	decreased mean corpuscular hemoglobin	Mon1b<em1(IMPC)J>/Mon1b<em1(IMPC)J>	C57BL/6NJ-Mon1b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317017	F	MP:0002591	decreased mean corpuscular volume	Mon1b<em1(IMPC)J>/Mon1b<em1(IMPC)J>	C57BL/6NJ-Mon1b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317017	F	MP:0002075	abnormal coat/hair pigmentation	Mon1b<em1(IMPC)J>/Mon1b<em1(IMPC)J>	C57BL/6NJ-Mon1b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317018	M	MP:0003131	increased erythrocyte cell number	Morn3<em1(IMPC)J>/Morn3<em1(IMPC)J>	C57BL/6NJ-Morn3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317019	F	MP:0010123	increased bone mineral content	Mrps36<em1(IMPC)Bay>/Mrps36<+>	C57BL/6N-Mrps36<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317019	F	MP:0010024	increased total body fat amount	Mrps36<em1(IMPC)Bay>/Mrps36<+>	C57BL/6N-Mrps36<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317019	F	MP:0003961	decreased lean body mass	Mrps36<em1(IMPC)Bay>/Mrps36<+>	C57BL/6N-Mrps36<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317019	F	MP:0003795	abnormal bone structure	Mrps36<em1(IMPC)Bay>/Mrps36<+>	C57BL/6N-Mrps36<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317019	F	MP:0003733	abnormal retina inner nuclear layer morphology	Mrps36<em1(IMPC)Bay>/Mrps36<+>	C57BL/6N-Mrps36<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317019	F	MP:0011959	abnormal eye posterior chamber depth	Mrps36<em1(IMPC)Bay>/Mrps36<+>	C57BL/6N-Mrps36<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317021	F	MP:0030610	absent teeth	Myzap<em1(IMPC)J>/Myzap<em1(IMPC)J>	C57BL/6NJ-Myzap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317021	F	MP:0005179	decreased circulating cholesterol level	Myzap<em1(IMPC)J>/Myzap<em1(IMPC)J>	C57BL/6NJ-Myzap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317021	F	MP:0005419	decreased circulating serum albumin level	Myzap<em1(IMPC)J>/Myzap<em1(IMPC)J>	C57BL/6NJ-Myzap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317021	F	MP:0005567	decreased circulating total protein level	Myzap<em1(IMPC)J>/Myzap<em1(IMPC)J>	C57BL/6NJ-Myzap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317021	F	MP:0000186	decreased circulating HDL cholesterol level	Myzap<em1(IMPC)J>/Myzap<em1(IMPC)J>	C57BL/6NJ-Myzap<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317022	F	MP:0001566	increased circulating phosphate level	Naa35<em1(IMPC)J>/Naa35<+>	C57BL/6NJ-Naa35<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317022	F	MP:0000221	decreased leukocyte cell number	Naa35<em1(IMPC)J>/Naa35<+>	C57BL/6NJ-Naa35<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317023	M	MP:0001284	absent vibrissae	Nap1l5<em1(IMPC)J>/Nap1l5<em1(IMPC)J>	C57BL/6NJ-Nap1l5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317024	F	MP:0005343	increased circulating aspartate transaminase level	Ncapd3<em1(IMPC)J>/Ncapd3<+>	C57BL/6NJ-Ncapd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317024	M	MP:0005178	increased circulating cholesterol level	Ncapd3<em1(IMPC)J>/Ncapd3<+>	C57BL/6NJ-Ncapd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317024	M	MP:0001556	increased circulating HDL cholesterol level	Ncapd3<em1(IMPC)J>/Ncapd3<+>	C57BL/6NJ-Ncapd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317029	F	MP:0011100	preweaning lethality, complete penetrance	Nudcd2<em1(IMPC)Bay>/Nudcd2<em1(IMPC)Bay>	C57BL/6N-Nudcd2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317030	M	MP:0000218	increased leukocyte cell number	Ociad1<em1(IMPC)J>/Ociad1<em1(IMPC)J>	C57BL/6NJ-Ociad1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317030	F	MP:0005559	increased circulating glucose level	Ociad1<em1(IMPC)J>/Ociad1<em1(IMPC)J>	C57BL/6NJ-Ociad1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317030	M	MP:0005293	impaired glucose tolerance	Ociad1<em1(IMPC)J>/Ociad1<em1(IMPC)J>	C57BL/6NJ-Ociad1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317030	F	MP:0001566	increased circulating phosphate level	Ociad1<em1(IMPC)J>/Ociad1<em1(IMPC)J>	C57BL/6NJ-Ociad1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317031	F	MP:0003731	abnormal retina outer nuclear layer morphology	Orai3<em1(IMPC)Bay>/Orai3<em1(IMPC)Bay>	C57BL/6N-Orai3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317033	M	MP:0005343	increased circulating aspartate transaminase level	Papola<em1(IMPC)J>/Papola<+>	C57BL/6NJ-Papola<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317033	M	MP:0003961	decreased lean body mass	Papola<em1(IMPC)J>/Papola<+>	C57BL/6NJ-Papola<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317034	M	MP:0002875	decreased erythrocyte cell number	Pcdhb22<tm1.1(KOMP)Vlcg>/Pcdhb22<tm1.1(KOMP)Vlcg>	C57BL/6N-Pcdhb22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:7317034	F	MP:0001513	limb grasping	Pcdhb22<tm1.1(KOMP)Vlcg>/Pcdhb22<tm1.1(KOMP)Vlcg>	C57BL/6N-Pcdhb22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:7317034	M	MP:0000208	decreased hematocrit	Pcdhb22<tm1.1(KOMP)Vlcg>/Pcdhb22<tm1.1(KOMP)Vlcg>	C57BL/6N-Pcdhb22<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:7317035	F	MP:0003795	abnormal bone structure	Pcif1<em1(IMPC)Bay>/Pcif1<em1(IMPC)Bay>	C57BL/6N-Pcif1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317035	F	MP:0001399	hyperactivity	Pcif1<em1(IMPC)Bay>/Pcif1<em1(IMPC)Bay>	C57BL/6N-Pcif1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317035	F	MP:0008259	abnormal optic disk morphology	Pcif1<em1(IMPC)Bay>/Pcif1<em1(IMPC)Bay>	C57BL/6N-Pcif1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317035	M	MP:0010025	decreased total body fat amount	Pcif1<em1(IMPC)Bay>/Pcif1<em1(IMPC)Bay>	C57BL/6N-Pcif1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317035	M	MP:0011110	preweaning lethality, incomplete penetrance	Pcif1<em1(IMPC)Bay>/Pcif1<em1(IMPC)Bay>	C57BL/6N-Pcif1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317035	F	MP:0001325	abnormal retina morphology	Pcif1<em1(IMPC)Bay>/Pcif1<em1(IMPC)Bay>	C57BL/6N-Pcif1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317035	M	MP:0003960	increased lean body mass	Pcif1<em1(IMPC)Bay>/Pcif1<em1(IMPC)Bay>	C57BL/6N-Pcif1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317035	M	MP:0001258	decreased body length	Pcif1<em1(IMPC)Bay>/Pcif1<em1(IMPC)Bay>	C57BL/6N-Pcif1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317035	F	MP:0003731	abnormal retina outer nuclear layer morphology	Pcif1<em1(IMPC)Bay>/Pcif1<em1(IMPC)Bay>	C57BL/6N-Pcif1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317039	M	MP:0001293	anophthalmia	Pign<em1(IMPC)Mbp>/Pign<em1(IMPC)Mbp>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317039	M	MP:0000914	exencephaly	Pign<em1(IMPC)Mbp>/Pign<em1(IMPC)Mbp>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317039	M	MP:0008797	facial cleft	Pign<em1(IMPC)Mbp>/Pign<em1(IMPC)Mbp>	C57BL/6N-Pign<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317041	M	MP:0011962	increased cornea thickness	Pnldc1<em1(IMPC)Bay>/Pnldc1<em1(IMPC)Bay>	C57BL/6N-Pnldc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317041	M	MP:0001925	male infertility	Pnldc1<em1(IMPC)Bay>/Pnldc1<em1(IMPC)Bay>	C57BL/6N-Pnldc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317047	F	MP:0000266	abnormal heart morphology	Prdm1<em1(IMPC)Bay>/Prdm1<em1(IMPC)Bay>	C57BL/6N-Prdm1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317048	M	MP:0003961	decreased lean body mass	Preb<em1(IMPC)J>/Preb<+>	C57BL/6NJ-Preb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317048	M	MP:0010024	increased total body fat amount	Preb<em1(IMPC)J>/Preb<+>	C57BL/6NJ-Preb<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317049	M	MP:0005178	increased circulating cholesterol level	Prr5<em1(IMPC)J>/Prr5<em1(IMPC)J>	C57BL/6NJ-Prr5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317049	M	MP:0010024	increased total body fat amount	Prr5<em1(IMPC)J>/Prr5<em1(IMPC)J>	C57BL/6NJ-Prr5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317049	M	MP:0001556	increased circulating HDL cholesterol level	Prr5<em1(IMPC)J>/Prr5<em1(IMPC)J>	C57BL/6NJ-Prr5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317049	M	MP:0003961	decreased lean body mass	Prr5<em1(IMPC)J>/Prr5<em1(IMPC)J>	C57BL/6NJ-Prr5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317051	F	MP:0013763	increased T-helper cell number	Pstpip1<em1(IMPC)Ccpcz>/Pstpip1<em1(IMPC)Ccpcz>	C57BL/6N-Pstpip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7317051	M	MP:0005628	decreased circulating potassium level	Pstpip1<em1(IMPC)Ccpcz>/Pstpip1<em1(IMPC)Ccpcz>	C57BL/6N-Pstpip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7317051	F	MP:0005568	increased circulating total protein level	Pstpip1<em1(IMPC)Ccpcz>/Pstpip1<em1(IMPC)Ccpcz>	C57BL/6N-Pstpip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7317051	M	MP:0000689	abnormal spleen morphology	Pstpip1<em1(IMPC)Ccpcz>/Pstpip1<em1(IMPC)Ccpcz>	C57BL/6N-Pstpip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7317051	F	MP:0002135	abnormal kidney morphology	Pstpip1<em1(IMPC)Ccpcz>/Pstpip1<em1(IMPC)Ccpcz>	C57BL/6N-Pstpip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7317051	F	MP:0000703	abnormal thymus morphology	Pstpip1<em1(IMPC)Ccpcz>/Pstpip1<em1(IMPC)Ccpcz>	C57BL/6N-Pstpip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7317051	M	MP:0000599	enlarged liver	Pstpip1<em1(IMPC)Ccpcz>/Pstpip1<em1(IMPC)Ccpcz>	C57BL/6N-Pstpip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7317051	F	MP:0000709	enlarged thymus	Pstpip1<em1(IMPC)Ccpcz>/Pstpip1<em1(IMPC)Ccpcz>	C57BL/6N-Pstpip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7317051	F	MP:0003917	increased kidney weight	Pstpip1<em1(IMPC)Ccpcz>/Pstpip1<em1(IMPC)Ccpcz>	C57BL/6N-Pstpip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7317051	M	MP:0000598	abnormal liver morphology	Pstpip1<em1(IMPC)Ccpcz>/Pstpip1<em1(IMPC)Ccpcz>	C57BL/6N-Pstpip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7317051	M	MP:0000162	lordosis	Pstpip1<em1(IMPC)Ccpcz>/Pstpip1<em1(IMPC)Ccpcz>	C57BL/6N-Pstpip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7317051	F	MP:0008074	increased CD4-positive, alpha-beta T cell number	Pstpip1<em1(IMPC)Ccpcz>/Pstpip1<em1(IMPC)Ccpcz>	C57BL/6N-Pstpip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7317051	M	MP:0000691	enlarged spleen	Pstpip1<em1(IMPC)Ccpcz>/Pstpip1<em1(IMPC)Ccpcz>	C57BL/6N-Pstpip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7317052	M	MP:0001304	cataract	Ptpn18<em1(IMPC)J>/Ptpn18<+>	C57BL/6NJ-Ptpn18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317052	M	MP:0006241	abnormal placement of pupils	Ptpn18<em1(IMPC)J>/Ptpn18<+>	C57BL/6NJ-Ptpn18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317053	M	MP:0005560	decreased circulating glucose level	Pus7<em1(IMPC)J>/Pus7<+>	C57BL/6NJ-Pus7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317054	M	MP:0003131	increased erythrocyte cell number	Rab3c<tm1b(EUCOMM)Wtsi>/Rab3c<tm1b(EUCOMM)Wtsi>	C57BL/6N-Rab3c<tm1b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:7317055	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Rab40b<em1(IMPC)J>/Rab40b<em1(IMPC)J>	C57BL/6NJ-Rab40b<em1(IMPC)J>/J	N	MGI:5576271
MGI:7317057	F	MP:0000195	decreased circulating calcium level	Reps2<em1(IMPC)J>/Reps2<em1(IMPC)J>	C57BL/6NJ-Reps2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317058	F	MP:0005278	abnormal cholesterol homeostasis	Rnf180<em1(IMPC)J>/Rnf180<em1(IMPC)J>	C57BL/6NJ-Rnf180<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317058	M	MP:0002590	increased mean corpuscular volume	Rnf180<em1(IMPC)J>/Rnf180<em1(IMPC)J>	C57BL/6NJ-Rnf180<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317058	F	MP:0000186	decreased circulating HDL cholesterol level	Rnf180<em1(IMPC)J>/Rnf180<em1(IMPC)J>	C57BL/6NJ-Rnf180<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317059	M	MP:0002574	increased vertical activity	Rnf220<em1(IMPC)Bay>/Rnf220<+>	C57BL/6N-Rnf220<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317061	M	MP:0002699	abnormal vitreous body morphology	Ror2<em1(IMPC)Mbp>/Ror2<+>	C57BL/6N-Ror2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317061	M	MP:0002792	abnormal retina vasculature morphology	Ror2<em1(IMPC)Mbp>/Ror2<+>	C57BL/6N-Ror2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317061	M	MP:0001304	cataract	Ror2<em1(IMPC)Mbp>/Ror2<+>	C57BL/6N-Ror2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317062	M	MP:0001417	decreased exploration in new environment	Rps20<em1(IMPC)Bay>/Rps20<+>	C57BL/6N-Rps20<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317063	F	MP:0005559	increased circulating glucose level	Scml4<em1(IMPC)J>/Scml4<em1(IMPC)J>	C57BL/6NJ-Scml4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317067	M	MP:0003054	spina bifida	Shroom3<em1(IMPC)Bay>/Shroom3<em1(IMPC)Bay>	C57BL/6N-Shroom3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317069	F	MP:0010052	increased grip strength	Slc17a1<em1(IMPC)J>/Slc17a1<em1(IMPC)J>	C57BL/6NJ-Slc17a1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317070	M	MP:0011962	increased cornea thickness	Slc30a7<em1(IMPC)Bay>/Slc30a7<+>	C57BL/6N-Slc30a7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317071	F	MP:0001258	decreased body length	Slc38a3<em1(IMPC)Bay>/Slc38a3<+>	C57BL/6N-Slc38a3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317071	F	MP:0003795	abnormal bone structure	Slc38a3<em1(IMPC)Bay>/Slc38a3<+>	C57BL/6N-Slc38a3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317071	F	MP:0010123	increased bone mineral content	Slc38a3<em1(IMPC)Bay>/Slc38a3<+>	C57BL/6N-Slc38a3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317074	M	MP:0010506	prolonged RR interval	Spty2d1<em1(IMPC)J>/Spty2d1<+>	C57BL/6NJ-Spty2d1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317076	M	MP:0005344	increased circulating bilirubin level	Tbc1d31<em1(IMPC)J>/Tbc1d31<em1(IMPC)J>	C57BL/6NJ-Tbc1d31<em1(IMPC)J>/J	N	MGI:5576271
MGI:7317076	F	MP:0005553	increased circulating creatinine level	Tbc1d31<em1(IMPC)J>/Tbc1d31<em1(IMPC)J>	C57BL/6NJ-Tbc1d31<em1(IMPC)J>/J	N	MGI:5576271
MGI:7317078	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Thoc7<em1(IMPC)J>/Thoc7<+>	C57BL/6NJ-Thoc7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317079	M	MP:0000218	increased leukocyte cell number	Tifab<em1(IMPC)J>/Tifab<em1(IMPC)J>	C57BL/6NJ-Tifab<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317079	M	MP:0003960	increased lean body mass	Tifab<em1(IMPC)J>/Tifab<em1(IMPC)J>	C57BL/6NJ-Tifab<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317080	F	MP:0010123	increased bone mineral content	Tlk2<em1(IMPC)Bay>/Tlk2<+>	C57BL/6N-Tlk2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317080	F	MP:0003795	abnormal bone structure	Tlk2<em1(IMPC)Bay>/Tlk2<+>	C57BL/6N-Tlk2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317081	M	MP:0001925	male infertility	Tmc5<em1(IMPC)J>/Tmc5<em1(IMPC)J>	C57BL/6NJ-Tmc5<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317082	F	MP:0000691	enlarged spleen	Tmcc2<em1(IMPC)Mbp>/Tmcc2<+>	C57BL/6N-Tmcc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317082	F	MP:0002060	abnormal skin morphology	Tmcc2<em1(IMPC)Mbp>/Tmcc2<+>	C57BL/6N-Tmcc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317082	F	MP:0009342	enlarged gallbladder	Tmcc2<em1(IMPC)Mbp>/Tmcc2<+>	C57BL/6N-Tmcc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317082	F	MP:0001289	persistence of hyaloid vascular system	Tmcc2<em1(IMPC)Mbp>/Tmcc2<+>	C57BL/6N-Tmcc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317082	M	MP:0002591	decreased mean corpuscular volume	Tmcc2<em1(IMPC)Mbp>/Tmcc2<+>	C57BL/6N-Tmcc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317082	F	MP:0005084	abnormal gallbladder morphology	Tmcc2<em1(IMPC)Mbp>/Tmcc2<+>	C57BL/6N-Tmcc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317082	F	MP:0000689	abnormal spleen morphology	Tmcc2<em1(IMPC)Mbp>/Tmcc2<+>	C57BL/6N-Tmcc2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317085	M	MP:0001489	decreased startle reflex	Tram1<em1(IMPC)J>/Tram1<em1(IMPC)J>	C57BL/6NJ-Tram1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317085	F	MP:0003961	decreased lean body mass	Tram1<em1(IMPC)J>/Tram1<em1(IMPC)J>	C57BL/6NJ-Tram1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317085	M	MP:0005565	increased blood urea nitrogen level	Tram1<em1(IMPC)J>/Tram1<em1(IMPC)J>	C57BL/6NJ-Tram1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317085	M	MP:0005567	decreased circulating total protein level	Tram1<em1(IMPC)J>/Tram1<em1(IMPC)J>	C57BL/6NJ-Tram1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317085	F	MP:0003795	abnormal bone structure	Tram1<em1(IMPC)J>/Tram1<em1(IMPC)J>	C57BL/6NJ-Tram1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317085	M	MP:0001925	male infertility	Tram1<em1(IMPC)J>/Tram1<em1(IMPC)J>	C57BL/6NJ-Tram1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317085	F	MP:0010024	increased total body fat amount	Tram1<em1(IMPC)J>/Tram1<em1(IMPC)J>	C57BL/6NJ-Tram1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317085	F	MP:0010124	decreased bone mineral content	Tram1<em1(IMPC)J>/Tram1<em1(IMPC)J>	C57BL/6NJ-Tram1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317085	F	MP:0005635	decreased circulating bilirubin level	Tram1<em1(IMPC)J>/Tram1<em1(IMPC)J>	C57BL/6NJ-Tram1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317086	F	MP:0005553	increased circulating creatinine level	Trp53i11<em1(IMPC)J>/Trp53i11<em1(IMPC)J>	C57BL/6NJ-Trp53i11<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317089	F	MP:0010052	increased grip strength	U2af1<em1(IMPC)J>/U2af1<+>	C57BL/6NJ-U2af1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317089	M	MP:0001289	persistence of hyaloid vascular system	U2af1<em1(IMPC)J>/U2af1<+>	C57BL/6NJ-U2af1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317090	F	MP:0002968	increased circulating alkaline phosphatase level	Uckl1<em1(IMPC)J>/Uckl1<em1(IMPC)J>	C57BL/6NJ-Uckl1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317090	F	MP:0005562	decreased mean corpuscular hemoglobin	Uckl1<em1(IMPC)J>/Uckl1<em1(IMPC)J>	C57BL/6NJ-Uckl1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317090	F	MP:0003131	increased erythrocyte cell number	Uckl1<em1(IMPC)J>/Uckl1<em1(IMPC)J>	C57BL/6NJ-Uckl1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317091	F	MP:0005343	increased circulating aspartate transaminase level	Bltp3b<em1(IMPC)J>/Bltp3b<em1(IMPC)J>	C57BL/6NJ-Bltp3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317092	F	MP:0001325	abnormal retina morphology	Vangl2<em1(IMPC)Mbp>/Vangl2<+>	C57BL/6N-Vangl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317092	M	MP:0000198	decreased circulating phosphate level	Vangl2<em1(IMPC)Mbp>/Vangl2<+>	C57BL/6N-Vangl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317094	F	MP:0003131	increased erythrocyte cell number	Wdr53<em1(IMPC)J>/Wdr53<em1(IMPC)J>	C57BL/6NJ-Wdr53<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317094	F	MP:0002608	increased hematocrit	Wdr53<em1(IMPC)J>/Wdr53<em1(IMPC)J>	C57BL/6NJ-Wdr53<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317094	F	MP:0005344	increased circulating bilirubin level	Wdr53<em1(IMPC)J>/Wdr53<em1(IMPC)J>	C57BL/6NJ-Wdr53<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317094	F	MP:0005560	decreased circulating glucose level	Wdr53<em1(IMPC)J>/Wdr53<em1(IMPC)J>	C57BL/6NJ-Wdr53<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317097	M	MP:0001257	increased body length	Zfc3h1<em1(IMPC)Mbp>/Zfc3h1<+>	C57BL/6N-Zfc3h1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317097	F	MP:0000601	small liver	Zfc3h1<em1(IMPC)Mbp>/Zfc3h1<+>	C57BL/6N-Zfc3h1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317097	F	MP:0000598	abnormal liver morphology	Zfc3h1<em1(IMPC)Mbp>/Zfc3h1<+>	C57BL/6N-Zfc3h1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7317099	M	MP:0011959	abnormal eye posterior chamber depth	Zfp300<em1(IMPC)Bay>/Y	C57BL/6N-Zfp300<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7317100	F	MP:0002075	abnormal coat/hair pigmentation	Zfp438<em1(IMPC)J>/Zfp438<em1(IMPC)J>	C57BL/6NJ-Zfp438<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317101	M	MP:0000218	increased leukocyte cell number	Zfp638<em1(IMPC)J>/Zfp638<+>	C57BL/6NJ-Zfp638<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317101	F	MP:0005278	abnormal cholesterol homeostasis	Zfp638<em1(IMPC)J>/Zfp638<+>	C57BL/6NJ-Zfp638<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317102	M	MP:0005562	decreased mean corpuscular hemoglobin	Zfp7<em1(IMPC)J>/Zfp7<em1(IMPC)J>	C57BL/6NJ-Zfp7<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317103	F	MP:0001566	increased circulating phosphate level	Znhit1<em1(IMPC)J>/Znhit1<+>	C57BL/6NJ-Znhit1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317103	M	MP:0001510	abnormal coat appearance	Znhit1<em1(IMPC)J>/Znhit1<+>	C57BL/6NJ-Znhit1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317103	M	MP:0000367	abnormal coat/ hair morphology	Znhit1<em1(IMPC)J>/Znhit1<+>	C57BL/6NJ-Znhit1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317104	F	MP:0005561	increased mean corpuscular hemoglobin	Zswim6<em1(IMPC)J>/Zswim6<+>	C57BL/6NJ-Zswim6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317104	M	MP:0005655	increased aggression	Zswim6<em1(IMPC)J>/Zswim6<+>	C57BL/6NJ-Zswim6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317104	M	MP:0001289	persistence of hyaloid vascular system	Zswim6<em1(IMPC)J>/Zswim6<+>	C57BL/6NJ-Zswim6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7317104	F	MP:0001304	cataract	Zswim6<em1(IMPC)J>/Zswim6<+>	C57BL/6NJ-Zswim6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7327125	M	MP:0008892	abnormal sperm flagellum morphology	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0005578	teratozoospermia	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0001262	decreased body weight	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0009238	coiled sperm flagellum	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0009377	ectopic manchette	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0008893	detached sperm flagellum	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0031356	abnormal outer dense fiber morphology	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0009231	detached acrosome	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0008839	absent acrosome	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0020869	immotile sperm	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0009237	kinked sperm flagellum	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0008545	absent sperm flagellum	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0031374	abnormal manchette assembly	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0009239	short sperm flagellum	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0014052	increased male germ cell apoptosis	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0031351	abnormal sperm flagellum thickness	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0008898	abnormal acrosome morphology	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0001265	decreased body size	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0006380	abnormal spermatid morphology	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0031354	abnormal acrosome assembly	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0004852	decreased testis weight	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0031438	abnormal sperm radial spoke morphology	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0009230	abnormal sperm head morphology	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0009838	abnormal sperm axoneme morphology	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0002216	abnormal seminiferous tubule morphology	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0031352	absent sperm axonemal central pair	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0001147	small testis	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0031386	elongated manchette	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0001925	male infertility	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0009830	abnormal sperm connecting piece morphology	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0001732	postnatal growth retardation	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0002687	oligozoospermia	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327125	M	MP:0001932	abnormal spermiogenesis	Cfap65<em1Yqt>/Cfap65<em1Yqt>	involves: C57BL/6 * C57BL/6N	N	34231842
MGI:7327255	M	MP:0005159	azoospermia	Tesmin<em2Qsh>/Tesmin<em2Qsh>	involves: C57BL/6J	N	34388164
MGI:7327255	M	MP:0006379	abnormal spermatocyte morphology	Tesmin<em2Qsh>/Tesmin<em2Qsh>	involves: C57BL/6J	N	34388164
MGI:7327255	M	MP:0008261	arrest of male meiosis	Tesmin<em2Qsh>/Tesmin<em2Qsh>	involves: C57BL/6J	N	34388164
MGI:7327255	M	MP:0004852	decreased testis weight	Tesmin<em2Qsh>/Tesmin<em2Qsh>	involves: C57BL/6J	N	34388164
MGI:7327255	M	MP:0001147	small testis	Tesmin<em2Qsh>/Tesmin<em2Qsh>	involves: C57BL/6J	N	34388164
MGI:7327255	M	MP:0001925	male infertility	Tesmin<em2Qsh>/Tesmin<em2Qsh>	involves: C57BL/6J	N	34388164
MGI:7327255	M	MP:0014052	increased male germ cell apoptosis	Tesmin<em2Qsh>/Tesmin<em2Qsh>	involves: C57BL/6J	N	34388164
MGI:7327255	M	MP:0001155	arrest of spermatogenesis	Tesmin<em2Qsh>/Tesmin<em2Qsh>	involves: C57BL/6J	N	34388164
MGI:7327268	M	MP:0004852	decreased testis weight	Tesmin<em1Qsh>/Tesmin<em1Qsh>	involves: C57BL/6J	N	34388164
MGI:7327268	M	MP:0008261	arrest of male meiosis	Tesmin<em1Qsh>/Tesmin<em1Qsh>	involves: C57BL/6J	N	34388164
MGI:7327268	M	MP:0014052	increased male germ cell apoptosis	Tesmin<em1Qsh>/Tesmin<em1Qsh>	involves: C57BL/6J	N	34388164
MGI:7327268	M	MP:0001155	arrest of spermatogenesis	Tesmin<em1Qsh>/Tesmin<em1Qsh>	involves: C57BL/6J	N	34388164
MGI:7327268	M	MP:0001925	male infertility	Tesmin<em1Qsh>/Tesmin<em1Qsh>	involves: C57BL/6J	N	34388164
MGI:7327268	M	MP:0005159	azoospermia	Tesmin<em1Qsh>/Tesmin<em1Qsh>	involves: C57BL/6J	N	34388164
MGI:7327268	M	MP:0006379	abnormal spermatocyte morphology	Tesmin<em1Qsh>/Tesmin<em1Qsh>	involves: C57BL/6J	N	34388164
MGI:7327268	M	MP:0001147	small testis	Tesmin<em1Qsh>/Tesmin<em1Qsh>	involves: C57BL/6J	N	34388164
MGI:7327294	M	MP:0002687	oligozoospermia	Ccin<em2Gpt>/Ccin<em2Gpt>	C57BL/6JGpt-Ccin<em2Gpt>/Gpt	N	35793634
MGI:7327294	M	MP:0009230	abnormal sperm head morphology	Ccin<em2Gpt>/Ccin<em2Gpt>	C57BL/6JGpt-Ccin<em2Gpt>/Gpt	N	35793634
MGI:7327294	M	MP:0001925	male infertility	Ccin<em2Gpt>/Ccin<em2Gpt>	C57BL/6JGpt-Ccin<em2Gpt>/Gpt	N	35793634
MGI:7327294	M	MP:0002675	asthenozoospermia	Ccin<em2Gpt>/Ccin<em2Gpt>	C57BL/6JGpt-Ccin<em2Gpt>/Gpt	N	35793634
MGI:7327294	M	MP:0008898	abnormal acrosome morphology	Ccin<em2Gpt>/Ccin<em2Gpt>	C57BL/6JGpt-Ccin<em2Gpt>/Gpt	N	35793634
MGI:7327294	F	MP:0005389	reproductive system phenotype	Ccin<em2Gpt>/Ccin<em2Gpt>	C57BL/6JGpt-Ccin<em2Gpt>/Gpt	Y	35793634
MGI:7327294	M	MP:0014052	increased male germ cell apoptosis	Ccin<em2Gpt>/Ccin<em2Gpt>	C57BL/6JGpt-Ccin<em2Gpt>/Gpt	N	35793634
MGI:7327402	M	MP:0009234	absent sperm head	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	N	35547809
MGI:7327402	M	MP:0002675	asthenozoospermia	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	N	35547809
MGI:7327402	M	MP:0009830	abnormal sperm connecting piece morphology	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	N	35547809
MGI:7327402	M	MP:0004543	abnormal sperm physiology	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	N	35547809
MGI:7327402	M	MP:0002686	globozoospermia	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	N	35547809
MGI:7327402	M	MP:0031354	abnormal acrosome assembly	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	N	35547809
MGI:7327402	M	MP:0006380	abnormal spermatid morphology	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	N	35547809
MGI:7327402	M	MP:0001925	male infertility	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	N	35547809
MGI:7327402	M	MP:0009237	kinked sperm flagellum	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	N	35547809
MGI:7327402	M	MP:0002687	oligozoospermia	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	N	35547809
MGI:7327402	M	MP:0005389	reproductive system phenotype	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	Y	35547809
MGI:7327402	M	MP:0009647	decreased fertilization frequency	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	N	35547809
MGI:7327402	M	MP:0005578	teratozoospermia	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	N	35547809
MGI:7327402	M	MP:0031013	abnormal egg activation	Septin12<em1Lych>/Septin12<em1Lych>	C57BL/6-Septin12<em1Lych>	N	35547809
MGI:7327408	M	MP:0005389	reproductive system phenotype	Septin12<em1Lych>/Septin12<+>	C57BL/6-Septin12<em1Lych>	Y	35547809
MGI:7327514	M	MP:0005389	reproductive system phenotype	Zdhhc11<em1Mngx>/Zdhhc11<em1Mngx>	involves: C57BL/6	Y	34897408
MGI:7327516	M	MP:0014052	increased male germ cell apoptosis	Zdhhc19<em1Mngx>/Zdhhc19<em1Mngx>	involves: C57BL/6	N	34897408
MGI:7327516	M	MP:0001932	abnormal spermiogenesis	Zdhhc19<em1Mngx>/Zdhhc19<em1Mngx>	involves: C57BL/6	N	34897408
MGI:7327516	M	MP:0009230	abnormal sperm head morphology	Zdhhc19<em1Mngx>/Zdhhc19<em1Mngx>	involves: C57BL/6	N	34897408
MGI:7327516	M	MP:0001156	abnormal spermatogenesis	Zdhhc19<em1Mngx>/Zdhhc19<em1Mngx>	involves: C57BL/6	N	34897408
MGI:7327516	M	MP:0002687	oligozoospermia	Zdhhc19<em1Mngx>/Zdhhc19<em1Mngx>	involves: C57BL/6	N	34897408
MGI:7327516	M	MP:0005578	teratozoospermia	Zdhhc19<em1Mngx>/Zdhhc19<em1Mngx>	involves: C57BL/6	N	34897408
MGI:7327516	M	MP:0008892	abnormal sperm flagellum morphology	Zdhhc19<em1Mngx>/Zdhhc19<em1Mngx>	involves: C57BL/6	N	34897408
MGI:7327516	M	MP:0004852	decreased testis weight	Zdhhc19<em1Mngx>/Zdhhc19<em1Mngx>	involves: C57BL/6	N	34897408
MGI:7327516	M	MP:0002662	abnormal cauda epididymis morphology	Zdhhc19<em1Mngx>/Zdhhc19<em1Mngx>	involves: C57BL/6	N	34897408
MGI:7327516	M	MP:0020451	decreased sperm progressive motility	Zdhhc19<em1Mngx>/Zdhhc19<em1Mngx>	involves: C57BL/6	N	34897408
MGI:7327516	M	MP:0002675	asthenozoospermia	Zdhhc19<em1Mngx>/Zdhhc19<em1Mngx>	involves: C57BL/6	N	34897408
MGI:7327516	M	MP:0001925	male infertility	Zdhhc19<em1Mngx>/Zdhhc19<em1Mngx>	involves: C57BL/6	N	34897408
MGI:7327533	M	MP:0014052	increased male germ cell apoptosis	Cep250<em1Glvr>/Cep250<em1Glvr>	C57BL/6-Cep250<em1Glvr>	N	35127699
MGI:7327533	M	MP:0030943	abnormal centrosome morphology	Cep250<em1Glvr>/Cep250<em1Glvr>	C57BL/6-Cep250<em1Glvr>	N	35127699
MGI:7327533	M	MP:0008261	arrest of male meiosis	Cep250<em1Glvr>/Cep250<em1Glvr>	C57BL/6-Cep250<em1Glvr>	N	35127699
MGI:7327533	M	MP:0001147	small testis	Cep250<em1Glvr>/Cep250<em1Glvr>	C57BL/6-Cep250<em1Glvr>	N	35127699
MGI:7327533	M	MP:0005159	azoospermia	Cep250<em1Glvr>/Cep250<em1Glvr>	C57BL/6-Cep250<em1Glvr>	N	35127699
MGI:7327533	F	MP:0005389	reproductive system phenotype	Cep250<em1Glvr>/Cep250<em1Glvr>	C57BL/6-Cep250<em1Glvr>	Y	35127699
MGI:7327533	M	MP:0001925	male infertility	Cep250<em1Glvr>/Cep250<em1Glvr>	C57BL/6-Cep250<em1Glvr>	N	35127699
MGI:7327640	M	MP:0001156	abnormal spermatogenesis	Aldh1a1<tm1Gdu>/Aldh1a1<tm1Gdu>,Aldh1a2<tm1.1Mbp>/Aldh1a2<tm1.1Mbp>,Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	35574006
MGI:7327640	M	MP:0005159	azoospermia	Aldh1a1<tm1Gdu>/Aldh1a1<tm1Gdu>,Aldh1a2<tm1.1Mbp>/Aldh1a2<tm1.1Mbp>,Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	35574006
MGI:7327640	M	MP:0001925	male infertility	Aldh1a1<tm1Gdu>/Aldh1a1<tm1Gdu>,Aldh1a2<tm1.1Mbp>/Aldh1a2<tm1.1Mbp>,Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<+>	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	N	35574006
MGI:7327642	M	MP:0005389	reproductive system phenotype	Aldh1a1<tm1Gdu>/Aldh1a1<tm1Gdu>,Aldh1a2<tm1.1Mbp>/Aldh1a2<tm1.2Mbp>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6 * FVB/NJ	Y	35574006
MGI:7327644	M	MP:0001156	abnormal spermatogenesis	Aldh1a1<tm1Gdu>/Aldh1a1<tm1Gdu>,Aldh1a2<tm1.1Mbp>/Aldh1a2<tm1.2Mbp>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129 * C57BL/6 * SJL	N	35574006
MGI:7327644	M	MP:0001925	male infertility	Aldh1a1<tm1Gdu>/Aldh1a1<tm1Gdu>,Aldh1a2<tm1.1Mbp>/Aldh1a2<tm1.2Mbp>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129 * C57BL/6 * SJL	N	35574006
MGI:7327644	M	MP:0005159	azoospermia	Aldh1a1<tm1Gdu>/Aldh1a1<tm1Gdu>,Aldh1a2<tm1.1Mbp>/Aldh1a2<tm1.2Mbp>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129 * C57BL/6 * SJL	N	35574006
MGI:7327644	M	MP:0005250	decreased Sertoli cell number	Aldh1a1<tm1Gdu>/Aldh1a1<tm1Gdu>,Aldh1a2<tm1.1Mbp>/Aldh1a2<tm1.2Mbp>,Plekha5<Tg(AMH-cre)1Flor>/Plekha5<+>	involves: 129 * C57BL/6 * SJL	N	35574006
MGI:7327649	F	MP:0005389	reproductive system phenotype	Prmt1<tm1Hkim>/Prmt1<tm1Hkim>,Tg(Neurog3-cre)24Syos/0	Not Specified	Y	34360715
MGI:7327649	M	MP:0005159	azoospermia	Prmt1<tm1Hkim>/Prmt1<tm1Hkim>,Tg(Neurog3-cre)24Syos/0	Not Specified	N	34360715
MGI:7327649	M	MP:0001147	small testis	Prmt1<tm1Hkim>/Prmt1<tm1Hkim>,Tg(Neurog3-cre)24Syos/0	Not Specified	N	34360715
MGI:7327649	M	MP:0014052	increased male germ cell apoptosis	Prmt1<tm1Hkim>/Prmt1<tm1Hkim>,Tg(Neurog3-cre)24Syos/0	Not Specified	N	34360715
MGI:7327649	M	MP:0001154	seminiferous tubule degeneration	Prmt1<tm1Hkim>/Prmt1<tm1Hkim>,Tg(Neurog3-cre)24Syos/0	Not Specified	N	34360715
MGI:7327649	M	MP:0001925	male infertility	Prmt1<tm1Hkim>/Prmt1<tm1Hkim>,Tg(Neurog3-cre)24Syos/0	Not Specified	N	34360715
MGI:7327649	M	MP:0008261	arrest of male meiosis	Prmt1<tm1Hkim>/Prmt1<tm1Hkim>,Tg(Neurog3-cre)24Syos/0	Not Specified	N	34360715
MGI:7327651	M	MP:0005169	abnormal male meiosis	Mfn2<em1Cya>/Mfn2<em1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	35493072
MGI:7327651	M	MP:0001147	small testis	Mfn2<em1Cya>/Mfn2<em1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	35493072
MGI:7327651	M	MP:0001153	small seminiferous tubules	Mfn2<em1Cya>/Mfn2<em1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	35493072
MGI:7327651	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Mfn2<em1Cya>/Mfn2<em1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	35493072
MGI:7327651	M	MP:0009237	kinked sperm flagellum	Mfn2<em1Cya>/Mfn2<em1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	35493072
MGI:7327651	M	MP:0009232	abnormal sperm nucleus morphology	Mfn2<em1Cya>/Mfn2<em1Cya>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ	N	35493072
MGI:7328387	M	MP:0005389	reproductive system phenotype	Tex55<em2(IMPC)Ics>/Tex55<em2(IMPC)Ics>	C57BL/6N-Tex55<em2(IMPC)Ics>	Y	33458765
MGI:7328394	F	MP:0008059	abnormal podocyte foot process morphology	Stox1<tm1Rkl>/Stox1<tm1Rkl>	129-Stox1<tm1Rkl>	N	33301424
MGI:7328394	F	MP:0005376	homeostasis/metabolism phenotype	Stox1<tm1Rkl>/Stox1<tm1Rkl>	129-Stox1<tm1Rkl>	Y	33301424
MGI:7328394	F	MP:0011453	abnormal glomerular capillary endothelium morphology	Stox1<tm1Rkl>/Stox1<tm1Rkl>	129-Stox1<tm1Rkl>	N	33301424
MGI:7328394	F	MP:0012045	increased susceptibility to hypertension	Stox1<tm1Rkl>/Stox1<tm1Rkl>	129-Stox1<tm1Rkl>	N	33301424
MGI:7328394	F	MP:0009661	abnormal pregnancy	Stox1<tm1Rkl>/Stox1<tm1Rkl>	129-Stox1<tm1Rkl>	N	33301424
MGI:7328859	M	MP:0001488	increased startle reflex	Myt1l<em1Mwer>/Myt1l<+>	involves: C57BL/6N	N	35538503
MGI:7330193	F	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis	Dock10<tm1Thar>/Dock10<tm1Thar>	involves: C57BL/6	N	32241915
MGI:7331609	M	MP:0003109	short femur	Gt(ROSA)26Sor<em#(CAG-Fstl5)Jrio>/Gt(ROSA)26Sor<+>,Tg(Prrx1-cre)1Cjt/0	involves: C57BL/6J * C57BL/6N * SJL/J	N	33105483
MGI:7331609	M	MP:0020010	decreased bone mineral density of femur	Gt(ROSA)26Sor<em#(CAG-Fstl5)Jrio>/Gt(ROSA)26Sor<+>,Tg(Prrx1-cre)1Cjt/0	involves: C57BL/6J * C57BL/6N * SJL/J	N	33105483
MGI:7331609	M	MP:0010119	abnormal bone mineral density	Gt(ROSA)26Sor<em#(CAG-Fstl5)Jrio>/Gt(ROSA)26Sor<+>,Tg(Prrx1-cre)1Cjt/0	involves: C57BL/6J * C57BL/6N * SJL/J	N	33105483
MGI:7331609	M	MP:0002764	short tibia	Gt(ROSA)26Sor<em#(CAG-Fstl5)Jrio>/Gt(ROSA)26Sor<+>,Tg(Prrx1-cre)1Cjt/0	involves: C57BL/6J * C57BL/6N * SJL/J	N	33105483
MGI:7331657	F	MP:0003799	impaired macrophage chemotaxis	Dock11<tm1Thar>/Dock11<tm1Thar>	involves: C57BL/6	N	32241915
MGI:7331657	F	MP:0005387	immune system phenotype	Dock11<tm1Thar>/Dock11<tm1Thar>	involves: C57BL/6	Y	32241915
MGI:7331657	F	MP:0003631	nervous system phenotype	Dock11<tm1Thar>/Dock11<tm1Thar>	involves: C57BL/6	Y	32241915
MGI:7331657	F	MP:0005386	behavior/neurological phenotype	Dock11<tm1Thar>/Dock11<tm1Thar>	involves: C57BL/6	Y	32241915
MGI:7331657	F	MP:0005391	vision/eye phenotype	Dock11<tm1Thar>/Dock11<tm1Thar>	involves: C57BL/6	Y	32241915
MGI:7333158	M	MP:0002674	abnormal sperm motility	Del(6Spam1-Hyal5)1Eki/Del(6Spam1-Hyal5)1Eki	Not Specified	N	31670981
MGI:7333158	M	MP:0005389	reproductive system phenotype	Del(6Spam1-Hyal5)1Eki/Del(6Spam1-Hyal5)1Eki	Not Specified	Y	31670981
MGI:7333158	M	MP:0001935	decreased litter size	Del(6Spam1-Hyal5)1Eki/Del(6Spam1-Hyal5)1Eki	Not Specified	N	31670981
MGI:7333158	M	MP:0001922	reduced male fertility	Del(6Spam1-Hyal5)1Eki/Del(6Spam1-Hyal5)1Eki	Not Specified	N	31670981
MGI:7333158	M	MP:0000242	impaired fertilization	Del(6Spam1-Hyal5)1Eki/Del(6Spam1-Hyal5)1Eki	Not Specified	N	31670981
MGI:7333158	M	MP:0004543	abnormal sperm physiology	Del(6Spam1-Hyal5)1Eki/Del(6Spam1-Hyal5)1Eki	Not Specified	N	31670981
MGI:7333158	M	MP:0009647	decreased fertilization frequency	Del(6Spam1-Hyal5)1Eki/Del(6Spam1-Hyal5)1Eki	Not Specified	N	31670981
MGI:7333164	F	MP:0003845	abnormal decidualization	Pgr<tm2(cre)Lyd>/Pgr<+>,Rbpj<tm1Hon>/Rbpj<tm1Hon>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	N	30213224
MGI:7333169	M	MP:0005389	reproductive system phenotype	Dcaf12l1<em1Marp>/Y	C57BL/6J-Dcaf12l1<em1Marp>	Y	35850260
MGI:7333229	M	MP:0014052	increased male germ cell apoptosis	G3bp2<em1Smoc>/G3bp2<em1.1Smoc>,Tg(Stra8-icre)1Reb/0	B6.Cg-G3bp2<em1Smoc>/G3bp2<em1.1Smoc> Tg(Stra8-icre)1Reb	N	35782098
MGI:7333229	M	MP:0005389	reproductive system phenotype	G3bp2<em1Smoc>/G3bp2<em1.1Smoc>,Tg(Stra8-icre)1Reb/0	B6.Cg-G3bp2<em1Smoc>/G3bp2<em1.1Smoc> Tg(Stra8-icre)1Reb	N	35782098
MGI:7333231	M	MP:0014052	increased male germ cell apoptosis	G3bp2<em1Smoc>/G3bp2<em1.1Smoc>,Tg(Ddx4-cre)1Dcas/0	B6.Cg-G3bp2<em1Smoc>/G3bp2<em1.1Smoc> Tg(Ddx4-cre)1Dcas	N	35782098
MGI:7333231	M	MP:0005389	reproductive system phenotype	G3bp2<em1Smoc>/G3bp2<em1.1Smoc>,Tg(Ddx4-cre)1Dcas/0	B6.Cg-G3bp2<em1Smoc>/G3bp2<em1.1Smoc> Tg(Ddx4-cre)1Dcas	Y	35782098
MGI:7333320	M	MP:0001925	male infertility	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0014052	increased male germ cell apoptosis	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0002687	oligozoospermia	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0004543	abnormal sperm physiology	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0020451	decreased sperm progressive motility	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0002675	asthenozoospermia	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0004542	impaired acrosome reaction	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	F	MP:0005389	reproductive system phenotype	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	Y	35547804
MGI:7333320	M	MP:0011635	abnormal mitochondrial crista morphology	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0004901	decreased male germ cell number	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0001156	abnormal spermatogenesis	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0005169	abnormal male meiosis	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0009831	abnormal sperm midpiece morphology	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0009647	decreased fertilization frequency	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0003666	impaired sperm capacitation	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7333320	M	MP:0010948	abnormal double-strand DNA break repair	Tmprss12<em1Huizh>/Tmprss12<em1Huizh>	C57BL/6-Tmprss12<em1Huizh>	N	35547804
MGI:7336179	F	MP:0003107	abnormal response to novelty	Tusc2<tm1Avi>/Tusc2<tm1Avi>	involves: 129S1/Sv	N	28351997
MGI:7336179	M	MP:0002662	abnormal cauda epididymis morphology	Tusc2<tm1Avi>/Tusc2<tm1Avi>	involves: 129S1/Sv	N	28351997
MGI:7336179	F	MP:0009661	abnormal pregnancy	Tusc2<tm1Avi>/Tusc2<tm1Avi>	involves: 129S1/Sv	N	28351997
MGI:7336179	M	MP:0031210	small cauda epididymis	Tusc2<tm1Avi>/Tusc2<tm1Avi>	involves: 129S1/Sv	N	28351997
MGI:7336179	M	MP:0002997	enlarged seminal vesicle	Tusc2<tm1Avi>/Tusc2<tm1Avi>	involves: 129S1/Sv	N	28351997
MGI:7336179	M	MP:0001147	small testis	Tusc2<tm1Avi>/Tusc2<tm1Avi>	involves: 129S1/Sv	N	28351997
MGI:7336179	M	MP:0002687	oligozoospermia	Tusc2<tm1Avi>/Tusc2<tm1Avi>	involves: 129S1/Sv	N	28351997
MGI:7336179	M	MP:0013600	testis degeneration	Tusc2<tm1Avi>/Tusc2<tm1Avi>	involves: 129S1/Sv	N	28351997
MGI:7336179	F	MP:0001382	abnormal nursing	Tusc2<tm1Avi>/Tusc2<tm1Avi>	involves: 129S1/Sv	N	28351997
MGI:7336179	M	MP:0002675	asthenozoospermia	Tusc2<tm1Avi>/Tusc2<tm1Avi>	involves: 129S1/Sv	N	28351997
MGI:7336681	F	MP:0031392	hypoactivity	Leap2<em1Jmz>/Leap2<em1Jmz>	C57BL/6N-Leap2<em1Jmz>	N	34428557
MGI:7336681	F	MP:0004890	decreased energy expenditure	Leap2<em1Jmz>/Leap2<em1Jmz>	C57BL/6N-Leap2<em1Jmz>	N	34428557
MGI:7336681	F	MP:0001431	abnormal eating behavior	Leap2<em1Jmz>/Leap2<em1Jmz>	C57BL/6N-Leap2<em1Jmz>	N	34428557
MGI:7336681	F	MP:0005290	decreased oxygen consumption	Leap2<em1Jmz>/Leap2<em1Jmz>	C57BL/6N-Leap2<em1Jmz>	N	34428557
MGI:7336681	F	MP:0020234	decreased basal metabolism	Leap2<em1Jmz>/Leap2<em1Jmz>	C57BL/6N-Leap2<em1Jmz>	N	34428557
MGI:7336681	F	MP:0005658	increased susceptibility to diet-induced obesity	Leap2<em1Jmz>/Leap2<em1Jmz>	C57BL/6N-Leap2<em1Jmz>	N	34428557
MGI:7336681	F	MP:0003961	decreased lean body mass	Leap2<em1Jmz>/Leap2<em1Jmz>	C57BL/6N-Leap2<em1Jmz>	N	34428557
MGI:7336681	F	MP:0031115	macrovesicular hepatic steatosis	Leap2<em1Jmz>/Leap2<em1Jmz>	C57BL/6N-Leap2<em1Jmz>	N	34428557
MGI:7339154	M	MP:0005386	behavior/neurological phenotype	Lamp2<tm1.2Ces>/Y	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL	Y	34459252
MGI:7339154	M	MP:0014071	increased cardiac muscle glycogen level	Lamp2<tm1.2Ces>/Y	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL	N	34459252
MGI:7339154	M	MP:0011088	neonatal lethality, incomplete penetrance	Lamp2<tm1.2Ces>/Y	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL	N	34459252
MGI:7339154	M	MP:0002625	heart left ventricle hypertrophy	Lamp2<tm1.2Ces>/Y	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL	N	34459252
MGI:7339154	M	MP:0001625	cardiac hypertrophy	Lamp2<tm1.2Ces>/Y	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL	N	34459252
MGI:7339154	M	MP:0002833	increased heart weight	Lamp2<tm1.2Ces>/Y	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL	N	34459252
MGI:7339154	M	MP:0009703	decreased birth body size	Lamp2<tm1.2Ces>/Y	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL	N	34459252
MGI:7339154	M	MP:0005330	cardiomyopathy	Lamp2<tm1.2Ces>/Y	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL	N	34459252
MGI:7339154	M	MP:0002753	dilated heart left ventricle	Lamp2<tm1.2Ces>/Y	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL	N	34459252
MGI:7339154	M	MP:0001636	irregular heartbeat	Lamp2<tm1.2Ces>/Y	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL	N	34459252
MGI:7339154	M	MP:0003896	prolonged PR interval	Lamp2<tm1.2Ces>/Y	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL	N	34459252
MGI:7339154	M	MP:0031078	increased circulating troponin T level	Lamp2<tm1.2Ces>/Y	involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL	N	34459252
MGI:7339183	M	MP:0001405	impaired coordination	Chd7<tm2c(EUCOMM)Wtsi>/Chd7<tm2c(EUCOMM)Wtsi>,Tg(Atoh1-cre)1Bfri/0	involves: C57BL/6 * C57BL/6J * C57BL/6N * CBA	N	28165338
MGI:7341464	M	MP:0005370	liver/biliary system phenotype	Ftsj1<tm1Tomik>/Y	Not Specified	Y	33771871
MGI:7341464	M	MP:0001262	decreased body weight	Ftsj1<tm1Tomik>/Y	Not Specified	N	33771871
MGI:7343893	F	MP:0001716	abnormal placenta labyrinth morphology	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0000160	kyphosis	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0001297	microphthalmia	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0000585	kinked tail	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0001344	blepharoptosis	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0011086	postnatal lethality, incomplete penetrance	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0001698	decreased embryo size	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0001711	abnormal placenta morphology	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0008862	asymmetric snout	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0030189	broad snout	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0000111	cleft palate	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0001304	cataract	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0009397	increased trophoblast giant cell number	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0011523	thin placenta labyrinth	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0013293	embryonic lethality prior to tooth bud stage	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0004255	abnormal spongiotrophoblast layer morphology	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343893	F	MP:0011088	neonatal lethality, incomplete penetrance	Bcor<tm1.1Vjba>/Bcor<+>,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343894	M	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance	Bcor<tm1.1Vjba>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343894	M	MP:0012138	decreased forebrain size	Bcor<tm1.1Vjba>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343894	M	MP:0003984	embryonic growth retardation	Bcor<tm1.1Vjba>/Y,Tmem163<Tg(ACTB-cre)2Mrt>/Tmem163<+>	involves: 129S1/Sv * C57BL/6N * FVB/N	N	32692983
MGI:7343896	M	MP:0005385	cardiovascular system phenotype	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	Y	32692983
MGI:7343896	M	MP:0011087	neonatal lethality, complete penetrance	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	N	32692983
MGI:7343896	M	MP:0031443	abnormal tongue position	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	N	32692983
MGI:7343896	M	MP:0021213	complete cleft palate	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	N	32692983
MGI:7343896	M	MP:0009546	absent gastric milk in neonates	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	N	32692983
MGI:7343896	M	MP:0009886	failure of palatal shelf elevation	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	N	32692983
MGI:7343896	M	MP:0003717	pallor	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	N	32692983
MGI:7343896	M	MP:0000762	abnormal tongue morphology	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	N	32692983
MGI:7343896	M	MP:0009909	bifid tongue	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	N	32692983
MGI:7343896	M	MP:0013264	tongue ankylosis	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	N	32692983
MGI:7343896	M	MP:0003792	abnormal major salivary gland morphology	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	N	32692983
MGI:7343896	M	MP:0000088	short mandible	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	N	32692983
MGI:7343896	M	MP:0006020	decreased tympanic ring size	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	N	32692983
MGI:7343896	M	MP:0013933	short Meckel's cartilage	Bcor<tm1.1Vjba>/Y,Pax3<tm1(cre)Joe>/Pax3<+>	involves: 129S1/Sv * C57BL/6J	N	32692983
MGI:7343897	M	MP:0021213	complete cleft palate	Bcor<tm1.1Vjba>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S1/Sv * C57BL/6J * CBA/J	N	32692983
MGI:7343897	M	MP:0011087	neonatal lethality, complete penetrance	Bcor<tm1.1Vjba>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S1/Sv * C57BL/6J * CBA/J	N	32692983
MGI:7343897	M	MP:0003792	abnormal major salivary gland morphology	Bcor<tm1.1Vjba>/Y,H2az2<Tg(Wnt1-cre)11Rth>/H2az2<+>	involves: 129S1/Sv * C57BL/6J * CBA/J	N	32692983
MGI:7343918	M	MP:0011100	preweaning lethality, complete penetrance	Bcor<tm1.1Vjba>/Y,Isl1<tm1(cre)Sev>/Isl1<+>	involves: 129S1/Sv	N	32692983
MGI:7343918	M	MP:0010418	perimembraneous ventricular septal defect	Bcor<tm1.1Vjba>/Y,Isl1<tm1(cre)Sev>/Isl1<+>	involves: 129S1/Sv	N	32692983
MGI:7343918	M	MP:0000564	syndactyly	Bcor<tm1.1Vjba>/Y,Isl1<tm1(cre)Sev>/Isl1<+>	involves: 129S1/Sv	N	32692983
MGI:7343918	M	MP:0004113	abnormal aortic arch morphology	Bcor<tm1.1Vjba>/Y,Isl1<tm1(cre)Sev>/Isl1<+>	involves: 129S1/Sv	N	32692983
MGI:7343918	M	MP:0006208	lethality throughout fetal growth and development	Bcor<tm1.1Vjba>/Y,Isl1<tm1(cre)Sev>/Isl1<+>	involves: 129S1/Sv	N	32692983
MGI:7343918	M	MP:0002633	persistent truncus arteriosus	Bcor<tm1.1Vjba>/Y,Isl1<tm1(cre)Sev>/Isl1<+>	involves: 129S1/Sv	N	32692983
MGI:7343919	F	MP:0002633	persistent truncus arteriosus	Bcor<tm1.1Vjba>/Bcor<+>,Isl1<tm1(cre)Sev>/Isl1<+>	involves: 129S1/Sv	N	32692983
MGI:7343919	F	MP:0011110	preweaning lethality, incomplete penetrance	Bcor<tm1.1Vjba>/Bcor<+>,Isl1<tm1(cre)Sev>/Isl1<+>	involves: 129S1/Sv	N	32692983
MGI:7346429	M	MP:0002075	abnormal coat/hair pigmentation	Ctif<em1(IMPC)J>/Ctif<em1(IMPC)J>	C57BL/6NJ-Ctif<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7346429	F	MP:0005292	improved glucose tolerance	Ctif<em1(IMPC)J>/Ctif<em1(IMPC)J>	C57BL/6NJ-Ctif<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7346429	F	MP:0010507	shortened RR interval	Ctif<em1(IMPC)J>/Ctif<em1(IMPC)J>	C57BL/6NJ-Ctif<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7346429	F	MP:0002626	increased heart rate	Ctif<em1(IMPC)J>/Ctif<em1(IMPC)J>	C57BL/6NJ-Ctif<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7356607	M	MP:0002169	no abnormal phenotype detected	Rbm46<em2Rpc>/Rbm46<em2Rpc>	involves: C57BL/6J * SJL/J	N	36129965
MGI:7356608	M	MP:0004852	decreased testis weight	Rbm46<em1Rpc>/Rbm46<em1Rpc>	involves: C57BL/6J * SJL/J	N	36129965
MGI:7356608	M	MP:0001156	abnormal spermatogenesis	Rbm46<em1Rpc>/Rbm46<em1Rpc>	involves: C57BL/6J * SJL/J	N	36129965
MGI:7356608	F	MP:0004805	absent oocytes	Rbm46<em1Rpc>/Rbm46<em1Rpc>	involves: C57BL/6J * SJL/J	N	36129965
MGI:7356608	M	MP:0001155	arrest of spermatogenesis	Rbm46<em1Rpc>/Rbm46<em1Rpc>	involves: C57BL/6J * SJL/J	N	36129965
MGI:7356608	M	MP:0001147	small testis	Rbm46<em1Rpc>/Rbm46<em1Rpc>	involves: C57BL/6J * SJL/J	N	36129965
MGI:7356612	M	MP:0004852	decreased testis weight	Rbm46<em3Rpc>/Rbm46<em3Rpc>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ * SJL/J	N	36129965
MGI:7356612	M	MP:0001156	abnormal spermatogenesis	Rbm46<em3Rpc>/Rbm46<em3Rpc>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ * SJL/J	N	36129965
MGI:7356612	M	MP:0001147	small testis	Rbm46<em3Rpc>/Rbm46<em3Rpc>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6J * FVB/NJ * SJL/J	N	36129965
MGI:7356658	M	MP:0002675	asthenozoospermia	Xpo4<em1Gshan>/Xpo4<+>	involves: C57BL/6J	N	36182935
MGI:7356658	M	MP:0009234	absent sperm head	Xpo4<em1Gshan>/Xpo4<+>	involves: C57BL/6J	N	36182935
MGI:7356658	M	MP:0001147	small testis	Xpo4<em1Gshan>/Xpo4<+>	involves: C57BL/6J	N	36182935
MGI:7356658	M	MP:0001925	male infertility	Xpo4<em1Gshan>/Xpo4<+>	involves: C57BL/6J	N	36182935
MGI:7356658	M	MP:0009238	coiled sperm flagellum	Xpo4<em1Gshan>/Xpo4<+>	involves: C57BL/6J	N	36182935
MGI:7356658	M	MP:0005578	teratozoospermia	Xpo4<em1Gshan>/Xpo4<+>	involves: C57BL/6J	N	36182935
MGI:7356658	M	MP:0020451	decreased sperm progressive motility	Xpo4<em1Gshan>/Xpo4<+>	involves: C57BL/6J	N	36182935
MGI:7356658	M	MP:0002687	oligozoospermia	Xpo4<em1Gshan>/Xpo4<+>	involves: C57BL/6J	N	36182935
MGI:7356658	M	MP:0004884	abnormal testis physiology	Xpo4<em1Gshan>/Xpo4<+>	involves: C57BL/6J	N	36182935
MGI:7356698	F	MP:0005567	decreased circulating total protein level	H2az1<em1(IMPC)J>/H2az1<+>	C57BL/6NJ-H2az1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7367286	F	MP:0003928	increased heart rate variability	Rr303<em1Vave>/Rr303<em1Vave>	Not Specified	N	33044128
MGI:7367370	M	MP:0009838	abnormal sperm axoneme morphology	Kpna4<tm1Maoka>/Kpna4<tm1Maoka>	B6.Cg-Kpna4<tm1Maoka>	N	33058343
MGI:7367370	M	MP:0000242	impaired fertilization	Kpna4<tm1Maoka>/Kpna4<tm1Maoka>	B6.Cg-Kpna4<tm1Maoka>	N	33058343
MGI:7367370	M	MP:0004542	impaired acrosome reaction	Kpna4<tm1Maoka>/Kpna4<tm1Maoka>	B6.Cg-Kpna4<tm1Maoka>	N	33058343
MGI:7367370	M	MP:0020451	decreased sperm progressive motility	Kpna4<tm1Maoka>/Kpna4<tm1Maoka>	B6.Cg-Kpna4<tm1Maoka>	N	33058343
MGI:7367370	M	MP:0009230	abnormal sperm head morphology	Kpna4<tm1Maoka>/Kpna4<tm1Maoka>	B6.Cg-Kpna4<tm1Maoka>	N	33058343
MGI:7367370	M	MP:0001922	reduced male fertility	Kpna4<tm1Maoka>/Kpna4<tm1Maoka>	B6.Cg-Kpna4<tm1Maoka>	N	33058343
MGI:7367370	M	MP:0008892	abnormal sperm flagellum morphology	Kpna4<tm1Maoka>/Kpna4<tm1Maoka>	B6.Cg-Kpna4<tm1Maoka>	N	33058343
MGI:7367524	M	MP:0008545	absent sperm flagellum	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0009838	abnormal sperm axoneme morphology	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0009230	abnormal sperm head morphology	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0031386	elongated manchette	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0009376	abnormal manchette morphology	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0002687	oligozoospermia	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0008892	abnormal sperm flagellum morphology	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0031352	absent sperm axonemal central pair	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0014467	increased sperm mitochondrial size	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0031356	abnormal outer dense fiber morphology	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0009238	coiled sperm flagellum	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0001156	abnormal spermatogenesis	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0009231	detached acrosome	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0001925	male infertility	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0009239	short sperm flagellum	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0030591	absent sperm fibrous sheath	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367524	M	MP:0020869	immotile sperm	Lrrc46<em1Cya>/Lrrc46<em1Cya>	C57BL/6N-Lrrc46<em1Cya>	N	35955660
MGI:7367546	M	MP:0001475	reduced long-term depression	Rr305<em1Drf>/Rr305<em1Drf>	Not Specified	N	34388204
MGI:7367577	M	MP:0002687	oligozoospermia	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367577	M	MP:0004852	decreased testis weight	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367577	M	MP:0002675	asthenozoospermia	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367577	M	MP:0005187	abnormal penis morphology	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367577	M	MP:0004910	decreased seminal vesicle weight	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367577	M	MP:0004929	decreased epididymis weight	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367577	M	MP:0004901	decreased male germ cell number	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367577	M	MP:0002286	cryptorchism	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367577	M	MP:0005250	decreased Sertoli cell number	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367577	M	MP:0009104	small penile bone	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367577	M	MP:0001922	reduced male fertility	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367577	M	MP:0001147	small testis	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367577	M	MP:0000519	hydronephrosis	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367577	M	MP:0005188	small penis	Kctd13<em1Djla>/Kctd13<em1Djla>	Not Specified	N	36196997
MGI:7367643	M	MP:0002874	decreased hemoglobin content	Dynlt4<tm1e(EUCOMM)Wtsi>/Dynlt4<tm1e(EUCOMM)Wtsi>	C57BL/6N-Dynlt4<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:7367643	M	MP:0000208	decreased hematocrit	Dynlt4<tm1e(EUCOMM)Wtsi>/Dynlt4<tm1e(EUCOMM)Wtsi>	C57BL/6N-Dynlt4<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:7367643	M	MP:0002875	decreased erythrocyte cell number	Dynlt4<tm1e(EUCOMM)Wtsi>/Dynlt4<tm1e(EUCOMM)Wtsi>	C57BL/6N-Dynlt4<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:7367644	M	MP:0005561	increased mean corpuscular hemoglobin	Fibp<tm1e(EUCOMM)Wtsi>/Fibp<+>	C57BL/6N-Fibp<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:7367644	M	MP:0002875	decreased erythrocyte cell number	Fibp<tm1e(EUCOMM)Wtsi>/Fibp<+>	C57BL/6N-Fibp<tm1e(EUCOMM)Wtsi>/Wtsi	N	MGI:5576271
MGI:7367646	M	MP:0001392	abnormal locomotor behavior	Micu1<tm1bNarl>/Micu1<tm1bNarl>	C57BL/6N-Micu1<tm1bNarl>/Narl	N	MGI:5576271
MGI:7367646	M	MP:0001406	abnormal gait	Micu1<tm1bNarl>/Micu1<tm1bNarl>	C57BL/6N-Micu1<tm1bNarl>/Narl	N	MGI:5576271
MGI:7367646	M	MP:0000443	abnormal snout morphology	Micu1<tm1bNarl>/Micu1<tm1bNarl>	C57BL/6N-Micu1<tm1bNarl>/Narl	N	MGI:5576271
MGI:7367646	M	MP:0011999	abnormal tail length	Micu1<tm1bNarl>/Micu1<tm1bNarl>	C57BL/6N-Micu1<tm1bNarl>/Narl	N	MGI:5576271
MGI:7367647	M	MP:0010124	decreased bone mineral content	Pcdh10<tm1bNarl>/Pcdh10<tm1bNarl>	C57BL/6N-Pcdh10<tm1bNarl>/Narl	N	MGI:5576271
MGI:7367647	M	MP:0001406	abnormal gait	Pcdh10<tm1bNarl>/Pcdh10<tm1bNarl>	C57BL/6N-Pcdh10<tm1bNarl>/Narl	N	MGI:5576271
MGI:7367647	F	MP:0001399	hyperactivity	Pcdh10<tm1bNarl>/Pcdh10<tm1bNarl>	C57BL/6N-Pcdh10<tm1bNarl>/Narl	N	MGI:5576271
MGI:7367648	F	MP:0001399	hyperactivity	Rasgrf1<tm1bNarl>/Rasgrf1<tm1bNarl>	C57BL/6N-Rasgrf1<tm1bNarl>/Narl	N	MGI:5576271
MGI:7367648	F	MP:0003960	increased lean body mass	Rasgrf1<tm1bNarl>/Rasgrf1<tm1bNarl>	C57BL/6N-Rasgrf1<tm1bNarl>/Narl	N	MGI:5576271
MGI:7367650	M	MP:0005016	decreased lymphocyte cell number	Yod1<tm1bNarl>/Yod1<tm1bNarl>	C57BL/6N-Yod1<tm1bNarl>/Narl	N	MGI:5576271
MGI:7367650	M	MP:0000219	increased neutrophil cell number	Yod1<tm1bNarl>/Yod1<tm1bNarl>	C57BL/6N-Yod1<tm1bNarl>/Narl	N	MGI:5576271
MGI:7367650	M	MP:0005343	increased circulating aspartate transaminase level	Yod1<tm1bNarl>/Yod1<tm1bNarl>	C57BL/6N-Yod1<tm1bNarl>/Narl	N	MGI:5576271
MGI:7367650	M	MP:0002941	increased circulating alanine transaminase level	Yod1<tm1bNarl>/Yod1<tm1bNarl>	C57BL/6N-Yod1<tm1bNarl>/Narl	N	MGI:5576271
MGI:7378518	M	MP:0009990	abnormal cerebellum vermis lobule III morphology	Zic3<Bn>/0	involves: BNT/LeJ * C57BL/6J	N	15450095
MGI:7378518	M	MP:0009959	abnormal cerebellar hemisphere morphology	Zic3<Bn>/0	involves: BNT/LeJ * C57BL/6J	N	15450095
MGI:7378518	M	MP:0031392	hypoactivity	Zic3<Bn>/0	involves: BNT/LeJ * C57BL/6J	N	15450095
MGI:7378518	M	MP:0000866	cerebellum vermis hypoplasia	Zic3<Bn>/0	involves: BNT/LeJ * C57BL/6J	N	15450095
MGI:7378518	M	MP:0001405	impaired coordination	Zic3<Bn>/0	involves: BNT/LeJ * C57BL/6J	N	15450095
MGI:7378518	M	MP:0011042	abnormal horizontal vestibuloocular reflex	Zic3<Bn>/0	involves: BNT/LeJ * C57BL/6J	N	15450095
MGI:7378518	M	MP:0005386	behavior/neurological phenotype	Zic3<Bn>/0	involves: BNT/LeJ * C57BL/6J	Y	15450095
MGI:7378518	M	MP:0009993	abnormal cerebellum vermis lobule V morphology	Zic3<Bn>/0	involves: BNT/LeJ * C57BL/6J	N	15450095
MGI:7380438	M	MP:0013899	abnormal seminal vesicle epithelium morphology	Herc6<tm1Kshim>/Herc6<tm1Kshim>	either: B6.Cg-Herc6<tm1Kshim> or (involves: C57BL/6NCrlj * CBA/JNCrlj)	N	25406959
MGI:7380438	M	MP:0002997	enlarged seminal vesicle	Herc6<tm1Kshim>/Herc6<tm1Kshim>	either: B6.Cg-Herc6<tm1Kshim> or (involves: C57BL/6NCrlj * CBA/JNCrlj)	N	25406959
MGI:7382756	M	MP:0008892	abnormal sperm flagellum morphology	4930463O16Rik<em1Bmpe>/4930463O16Rik<em1Bmpe>	C57BL/6N-4930463O16Rik<em1Bmpe>	N	34277642
MGI:7382756	M	MP:0002687	oligozoospermia	4930463O16Rik<em1Bmpe>/4930463O16Rik<em1Bmpe>	C57BL/6N-4930463O16Rik<em1Bmpe>	N	34277642
MGI:7382756	M	MP:0031426	increased sperm motility	4930463O16Rik<em1Bmpe>/4930463O16Rik<em1Bmpe>	C57BL/6N-4930463O16Rik<em1Bmpe>	N	34277642
MGI:7382756	M	MP:0002674	abnormal sperm motility	4930463O16Rik<em1Bmpe>/4930463O16Rik<em1Bmpe>	C57BL/6N-4930463O16Rik<em1Bmpe>	N	34277642
MGI:7382756	M	MP:0031427	increased sperm progressive motility	4930463O16Rik<em1Bmpe>/4930463O16Rik<em1Bmpe>	C57BL/6N-4930463O16Rik<em1Bmpe>	N	34277642
MGI:7384487	M	MP:0000266	abnormal heart morphology	Ark2n<em1Wehi>/Ark2n<em1Wehi>	C57BL/6J-8030462N17Rik<em1Wehi>	N	35882232
MGI:7384487	M	MP:0003961	decreased lean body mass	Ark2n<em1Wehi>/Ark2n<em1Wehi>	C57BL/6J-8030462N17Rik<em1Wehi>	N	35882232
MGI:7386897	M	MP:0001922	reduced male fertility	Teshl<em1Choc>/Teshl<em1Choc>	C57BL/6-1700027A15Rik<em1Choc>	N	34108217
MGI:7386897	M	MP:0009230	abnormal sperm head morphology	Teshl<em1Choc>/Teshl<em1Choc>	C57BL/6-1700027A15Rik<em1Choc>	N	34108217
MGI:7388729	F	MP:0001399	hyperactivity	Atp6v0b<em1(IMPC)J>/Atp6v0b<+>	C57BL/6NJ-Atp6v0b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7388729	F	MP:0001417	decreased exploration in new environment	Atp6v0b<em1(IMPC)J>/Atp6v0b<+>	C57BL/6NJ-Atp6v0b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7388729	F	MP:0001402	decreased locomotor activity	Atp6v0b<em1(IMPC)J>/Atp6v0b<+>	C57BL/6NJ-Atp6v0b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7388729	F	MP:0003795	abnormal bone structure	Atp6v0b<em1(IMPC)J>/Atp6v0b<+>	C57BL/6NJ-Atp6v0b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7388730	M	MP:0005559	increased circulating glucose level	Atp8a2<em1(IMPC)J>/Atp8a2<+>	C57BL/6NJ-Atp8a2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7388732	M	MP:0010052	increased grip strength	Camsap1<em1(IMPC)J>/Camsap1<+>	C57BL/6NJ-Camsap1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7388732	F	MP:0001566	increased circulating phosphate level	Camsap1<em1(IMPC)J>/Camsap1<+>	C57BL/6NJ-Camsap1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7388733	M	MP:0001925	male infertility	Cntrob<em1(IMPC)Bay>/Cntrob<em1(IMPC)Bay>	C57BL/6N-Cntrob<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388734	M	MP:0010088	decreased circulating fructosamine level	Col4a2<em1(IMPC)Wtsi>/Col4a2<+>	C57BL/6N-Col4a2<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:7388734	M	MP:0005567	decreased circulating total protein level	Col4a2<em1(IMPC)Wtsi>/Col4a2<+>	C57BL/6N-Col4a2<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:7388734	M	MP:0005419	decreased circulating serum albumin level	Col4a2<em1(IMPC)Wtsi>/Col4a2<+>	C57BL/6N-Col4a2<em1(IMPC)Wtsi>/WtsiOulu	N	MGI:5576271
MGI:7388736	F	MP:0001364	decreased anxiety-related response	Csf2rb<tm2b(EUCOMM)Hmgu>/Csf2rb<+>	C57BL/6N-Csf2rb<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:7388736	F	MP:0004924	abnormal behavior	Csf2rb<tm2b(EUCOMM)Hmgu>/Csf2rb<+>	C57BL/6N-Csf2rb<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:7388736	F	MP:0020870	decreased thigmotaxis	Csf2rb<tm2b(EUCOMM)Hmgu>/Csf2rb<+>	C57BL/6N-Csf2rb<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:7388736	F	MP:0005011	increased eosinophil cell number	Csf2rb<tm2b(EUCOMM)Hmgu>/Csf2rb<+>	C57BL/6N-Csf2rb<tm2b(EUCOMM)Hmgu>/Orl	N	MGI:5576271
MGI:7388739	F	MP:0001325	abnormal retina morphology	Gapdh<em1(IMPC)Mbp>/Gapdh<+>	C57BL/6N-Gapdh<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7388739	M	MP:0001304	cataract	Gapdh<em1(IMPC)Mbp>/Gapdh<+>	C57BL/6N-Gapdh<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7388741	F	MP:0009142	decreased prepulse inhibition	Lrsam1<em1(IMPC)Bay>/Lrsam1<em1(IMPC)Bay>	C57BL/6N-Lrsam1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388741	F	MP:0006203	eye hemorrhage	Lrsam1<em1(IMPC)Bay>/Lrsam1<em1(IMPC)Bay>	C57BL/6N-Lrsam1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388742	M	MP:0001925	male infertility	Mdc1<em1(IMPC)Bay>/Mdc1<em1(IMPC)Bay>	C57BL/6N-Mdc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388742	M	MP:0011952	decreased cardiac stroke volume	Mdc1<em1(IMPC)Bay>/Mdc1<em1(IMPC)Bay>	C57BL/6N-Mdc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388742	M	MP:0005140	decreased cardiac muscle contractility	Mdc1<em1(IMPC)Bay>/Mdc1<em1(IMPC)Bay>	C57BL/6N-Mdc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388742	M	MP:0003393	decreased cardiac output	Mdc1<em1(IMPC)Bay>/Mdc1<em1(IMPC)Bay>	C57BL/6N-Mdc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388746	M	MP:0001925	male infertility	Nphp4<em1(IMPC)Bay>/Nphp4<em1(IMPC)Bay>	C57BL/6N-Nphp4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388747	F	MP:0000219	increased neutrophil cell number	Nsg1<tm1.1(KOMP)Vlcg>/Nsg1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nsg1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7388747	F	MP:0005011	increased eosinophil cell number	Nsg1<tm1.1(KOMP)Vlcg>/Nsg1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nsg1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7388747	F	MP:0000218	increased leukocyte cell number	Nsg1<tm1.1(KOMP)Vlcg>/Nsg1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nsg1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7388747	M	MP:0006203	eye hemorrhage	Nsg1<tm1.1(KOMP)Vlcg>/Nsg1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nsg1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7388747	F	MP:0000220	increased monocyte cell number	Nsg1<tm1.1(KOMP)Vlcg>/Nsg1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nsg1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7388747	F	MP:0002606	increased basophil cell number	Nsg1<tm1.1(KOMP)Vlcg>/Nsg1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nsg1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7388747	M	MP:0002599	increased mean platelet volume	Nsg1<tm1.1(KOMP)Vlcg>/Nsg1<tm1.1(KOMP)Vlcg>	C57BL/6N-Nsg1<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7388750	M	MP:0000689	abnormal spleen morphology	Oas1c<em1(IMPC)Ccpcz>/Oas1c<em1(IMPC)Ccpcz>	C57BL/6N-Oas1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7388750	F	MP:0001293	anophthalmia	Oas1c<em1(IMPC)Ccpcz>/Oas1c<em1(IMPC)Ccpcz>	C57BL/6N-Oas1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7388750	F	MP:0002092	abnormal eye morphology	Oas1c<em1(IMPC)Ccpcz>/Oas1c<em1(IMPC)Ccpcz>	C57BL/6N-Oas1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7388750	F	MP:0002100	abnormal tooth morphology	Oas1c<em1(IMPC)Ccpcz>/Oas1c<em1(IMPC)Ccpcz>	C57BL/6N-Oas1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7388750	M	MP:0000692	small spleen	Oas1c<em1(IMPC)Ccpcz>/Oas1c<em1(IMPC)Ccpcz>	C57BL/6N-Oas1c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7388752	M	MP:0002965	increased circulating serum albumin level	Rab33a<em1(IMPC)H>/Y	C57BL/6N-Rab33a<em1(IMPC)H>/H	N	MGI:5576271
MGI:7388753	F	MP:0010393	shortened QRS complex duration	Rcan3<em1(IMPC)J>/Rcan3<em1(IMPC)J>	C57BL/6NJ-Rcan3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7388755	F	MP:0001697	abnormal embryo size	Slc30a9<em1(IMPC)Bay>/Slc30a9<+>	C57BL/6N-Slc30a9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388755	F	MP:0004258	abnormal placenta size	Slc30a9<em1(IMPC)Bay>/Slc30a9<+>	C57BL/6N-Slc30a9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388755	F	MP:0001712	abnormal placenta development	Slc30a9<em1(IMPC)Bay>/Slc30a9<+>	C57BL/6N-Slc30a9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388755	F	MP:0003984	embryonic growth retardation	Slc30a9<em1(IMPC)Bay>/Slc30a9<+>	C57BL/6N-Slc30a9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388758	F	MP:0011110	preweaning lethality, incomplete penetrance	Tchhl1<em1(IMPC)Bay>/Tchhl1<em1(IMPC)Bay>	C57BL/6N-Tchhl1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388761	F	MP:0001297	microphthalmia	Ugt1a6b<em1(IMPC)Bay>/Ugt1a6b<em1(IMPC)Bay>	C57BL/6N-Ugt1a6b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7388761	F	MP:0001293	anophthalmia	Ugt1a6b<em1(IMPC)Bay>/Ugt1a6b<em1(IMPC)Bay>	C57BL/6N-Ugt1a6b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7398572	M	MP:0009836	abnormal sperm principal piece morphology	Cep72<em1Lmgg>/Cep72<em1Lmgg>	C57BL/6N-Cep72<em1Lmgg>	N	36277211
MGI:7398572	M	MP:0009238	coiled sperm flagellum	Cep72<em1Lmgg>/Cep72<em1Lmgg>	C57BL/6N-Cep72<em1Lmgg>	N	36277211
MGI:7398572	M	MP:0005578	teratozoospermia	Cep72<em1Lmgg>/Cep72<em1Lmgg>	C57BL/6N-Cep72<em1Lmgg>	N	36277211
MGI:7398572	M	MP:0001932	abnormal spermiogenesis	Cep72<em1Lmgg>/Cep72<em1Lmgg>	C57BL/6N-Cep72<em1Lmgg>	N	36277211
MGI:7398572	M	MP:0009234	absent sperm head	Cep72<em1Lmgg>/Cep72<em1Lmgg>	C57BL/6N-Cep72<em1Lmgg>	N	36277211
MGI:7398572	M	MP:0009232	abnormal sperm nucleus morphology	Cep72<em1Lmgg>/Cep72<em1Lmgg>	C57BL/6N-Cep72<em1Lmgg>	N	36277211
MGI:7398572	M	MP:0009230	abnormal sperm head morphology	Cep72<em1Lmgg>/Cep72<em1Lmgg>	C57BL/6N-Cep72<em1Lmgg>	N	36277211
MGI:7398572	M	MP:0009838	abnormal sperm axoneme morphology	Cep72<em1Lmgg>/Cep72<em1Lmgg>	C57BL/6N-Cep72<em1Lmgg>	N	36277211
MGI:7398572	M	MP:0008839	absent acrosome	Cep72<em1Lmgg>/Cep72<em1Lmgg>	C57BL/6N-Cep72<em1Lmgg>	N	36277211
MGI:7398572	M	MP:0008892	abnormal sperm flagellum morphology	Cep72<em1Lmgg>/Cep72<em1Lmgg>	C57BL/6N-Cep72<em1Lmgg>	N	36277211
MGI:7398572	M	MP:0031356	abnormal outer dense fiber morphology	Cep72<em1Lmgg>/Cep72<em1Lmgg>	C57BL/6N-Cep72<em1Lmgg>	N	36277211
MGI:7407208	M	MP:0012465	increased hippocampal fimbria size	Magee2<em1(IMPC)Wtsi>/Y	C57BL/6N-Magee2<em1(IMPC)Wtsi>	N	34464968
MGI:7407208	M	MP:0005238	increased brain size	Magee2<em1(IMPC)Wtsi>/Y	C57BL/6N-Magee2<em1(IMPC)Wtsi>	N	34464968
MGI:7407208	M	MP:0012452	increased retrosplenial granular cortex size	Magee2<em1(IMPC)Wtsi>/Y	C57BL/6N-Magee2<em1(IMPC)Wtsi>	N	34464968
MGI:7407208	M	MP:0000434	megacephaly	Magee2<em1(IMPC)Wtsi>/Y	C57BL/6N-Magee2<em1(IMPC)Wtsi>	N	34464968
MGI:7407208	M	MP:0000905	increased superior colliculus size	Magee2<em1(IMPC)Wtsi>/Y	C57BL/6N-Magee2<em1(IMPC)Wtsi>	N	34464968
MGI:7407208	M	MP:0005378	growth/size/body region phenotype	Magee2<em1(IMPC)Wtsi>/Y	C57BL/6N-Magee2<em1(IMPC)Wtsi>	Y	34464968
MGI:7407208	M	MP:0012449	increased primary motor cortex size	Magee2<em1(IMPC)Wtsi>/Y	C57BL/6N-Magee2<em1(IMPC)Wtsi>	N	34464968
MGI:7407208	M	MP:0020534	increased pons size	Magee2<em1(IMPC)Wtsi>/Y	C57BL/6N-Magee2<em1(IMPC)Wtsi>	N	34464968
MGI:7407208	M	MP:0012451	abnormal retrosplenial granular cortex morphology	Magee2<em1(IMPC)Wtsi>/Y	C57BL/6N-Magee2<em1(IMPC)Wtsi>	N	34464968
MGI:7407208	M	MP:0008228	increased anterior commissure size	Magee2<em1(IMPC)Wtsi>/Y	C57BL/6N-Magee2<em1(IMPC)Wtsi>	N	34464968
MGI:7407217	F	MP:0003631	nervous system phenotype	Magee2<em1(IMPC)Wtsi>/Magee2<em1(IMPC)Wtsi>	C57BL/6N-Magee2<em1(IMPC)Wtsi>	Y	34464968
MGI:7408428	M	MP:0001925	male infertility	In(11)2Smun/In(11)2Smun	involves: C57BL/6J	N	31358994
MGI:7413054	M	MP:0001925	male infertility	Iqcn<em1Cya>/Iqcn<em1Cya>	C57BL/6J-Iqcn<em1Cya>	N	36321563
MGI:7413054	F	MP:0005389	reproductive system phenotype	Iqcn<em1Cya>/Iqcn<em1Cya>	C57BL/6J-Iqcn<em1Cya>	Y	36321563
MGI:7413054	M	MP:0031386	elongated manchette	Iqcn<em1Cya>/Iqcn<em1Cya>	C57BL/6J-Iqcn<em1Cya>	N	36321563
MGI:7413054	M	MP:0009647	decreased fertilization frequency	Iqcn<em1Cya>/Iqcn<em1Cya>	C57BL/6J-Iqcn<em1Cya>	N	36321563
MGI:7413054	M	MP:0008898	abnormal acrosome morphology	Iqcn<em1Cya>/Iqcn<em1Cya>	C57BL/6J-Iqcn<em1Cya>	N	36321563
MGI:7413054	M	MP:0004543	abnormal sperm physiology	Iqcn<em1Cya>/Iqcn<em1Cya>	C57BL/6J-Iqcn<em1Cya>	N	36321563
MGI:7413054	M	MP:0009377	ectopic manchette	Iqcn<em1Cya>/Iqcn<em1Cya>	C57BL/6J-Iqcn<em1Cya>	N	36321563
MGI:7413054	M	MP:0009230	abnormal sperm head morphology	Iqcn<em1Cya>/Iqcn<em1Cya>	C57BL/6J-Iqcn<em1Cya>	N	36321563
MGI:7413092	M	MP:0001925	male infertility	Iqub<em1Mngx>/Iqub<em1Mngx>	C57BL/6J-Iqub<em1Mngx>	N	36417862
MGI:7413092	M	MP:0008892	abnormal sperm flagellum morphology	Iqub<em1Mngx>/Iqub<em1Mngx>	C57BL/6J-Iqub<em1Mngx>	N	36417862
MGI:7413092	M	MP:0002675	asthenozoospermia	Iqub<em1Mngx>/Iqub<em1Mngx>	C57BL/6J-Iqub<em1Mngx>	N	36417862
MGI:7413092	M	MP:0020451	decreased sperm progressive motility	Iqub<em1Mngx>/Iqub<em1Mngx>	C57BL/6J-Iqub<em1Mngx>	N	36417862
MGI:7413092	F	MP:0005389	reproductive system phenotype	Iqub<em1Mngx>/Iqub<em1Mngx>	C57BL/6J-Iqub<em1Mngx>	Y	36417862
MGI:7413094	M	MP:0005389	reproductive system phenotype	Iqub<em2Mngx>/Iqub<em2Mngx>	C57BL/6J-Iqub<em2Mngx>	N	36417862
MGI:7413096	M	MP:0005389	reproductive system phenotype	Iqub<em3Mngx>/Iqub<em3Mngx>	C57BL/6J-Iqub<em3Mngx>	N	36417862
MGI:7413904	F	MP:0008870	increased mature ovarian follicle number	Abhd2<em1Lshko>/Abhd2<em1Lshko>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413904	F	MP:0005389	reproductive system phenotype	Abhd2<em1Lshko>/Abhd2<em1Lshko>	C57BL/6N-Abhd2<em1Lshko>	Y	34568325
MGI:7413904	F	MP:0031239	increased atretic ovarian follicle number	Abhd2<em1Lshko>/Abhd2<em1Lshko>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413904	F	MP:0009017	prolonged estrus	Abhd2<em1Lshko>/Abhd2<em1Lshko>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413904	F	MP:0001130	abnormal ovarian folliculogenesis	Abhd2<em1Lshko>/Abhd2<em1Lshko>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413904	F	MP:0009015	short proestrus	Abhd2<em1Lshko>/Abhd2<em1Lshko>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413904	F	MP:0013508	increased granulosa cell apoptosis	Abhd2<em1Lshko>/Abhd2<em1Lshko>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413904	F	MP:0031421	increased superovulation rate	Abhd2<em1Lshko>/Abhd2<em1Lshko>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413904	F	MP:0001126	abnormal ovary morphology	Abhd2<em1Lshko>/Abhd2<em1Lshko>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413904	F	MP:0009012	short diestrus	Abhd2<em1Lshko>/Abhd2<em1Lshko>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413904	F	MP:0001927	abnormal estrous cycle	Abhd2<em1Lshko>/Abhd2<em1Lshko>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413904	F	MP:0011129	decreased tertiary ovarian follicle number	Abhd2<em1Lshko>/Abhd2<em1Lshko>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413907	F	MP:0031421	increased superovulation rate	Abhd2<em1Lshko>/Abhd2<+>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413907	F	MP:0031239	increased atretic ovarian follicle number	Abhd2<em1Lshko>/Abhd2<+>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413907	F	MP:0008870	increased mature ovarian follicle number	Abhd2<em1Lshko>/Abhd2<+>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413907	F	MP:0002681	increased corpora lutea number	Abhd2<em1Lshko>/Abhd2<+>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413907	F	MP:0011129	decreased tertiary ovarian follicle number	Abhd2<em1Lshko>/Abhd2<+>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7413907	F	MP:0013508	increased granulosa cell apoptosis	Abhd2<em1Lshko>/Abhd2<+>	C57BL/6N-Abhd2<em1Lshko>	N	34568325
MGI:7414053	M	MP:0005389	reproductive system phenotype	C4bp<tm1Raw>/C4bp<tm1Raw>	B6.129-C4bp<tm1Raw>	Y	25468721
MGI:7414196	M	MP:0001552	increased circulating triglyceride level	Pcx<tm1c(EUCOMM)Wtsi>/Pcx<tm1c(EUCOMM)Wtsi>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * C57BL/6N * DBA * SJL	N	36441025
MGI:7414196	M	MP:0003564	abnormal insulin secretion	Pcx<tm1c(EUCOMM)Wtsi>/Pcx<tm1c(EUCOMM)Wtsi>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * C57BL/6N * DBA * SJL	N	36441025
MGI:7414196	M	MP:0003839	abnormal insulin clearance	Pcx<tm1c(EUCOMM)Wtsi>/Pcx<tm1c(EUCOMM)Wtsi>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * C57BL/6N * DBA * SJL	N	36441025
MGI:7414196	M	MP:0000609	abnormal liver physiology	Pcx<tm1c(EUCOMM)Wtsi>/Pcx<tm1c(EUCOMM)Wtsi>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * C57BL/6N * DBA * SJL	N	36441025
MGI:7414196	M	MP:0013242	abnormal amino acid metabolism	Pcx<tm1c(EUCOMM)Wtsi>/Pcx<tm1c(EUCOMM)Wtsi>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * C57BL/6N * DBA * SJL	N	36441025
MGI:7414196	M	MP:0002628	hepatic steatosis	Pcx<tm1c(EUCOMM)Wtsi>/Pcx<tm1c(EUCOMM)Wtsi>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * C57BL/6N * DBA * SJL	N	36441025
MGI:7414196	F	MP:0003917	increased kidney weight	Pcx<tm1c(EUCOMM)Wtsi>/Pcx<tm1c(EUCOMM)Wtsi>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * C57BL/6N * DBA * SJL	N	36441025
MGI:7414196	M	MP:0005292	improved glucose tolerance	Pcx<tm1c(EUCOMM)Wtsi>/Pcx<tm1c(EUCOMM)Wtsi>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * C57BL/6N * DBA * SJL	N	36441025
MGI:7414762	M	MP:0002098	abnormal vibrissa morphology	1810055G02Rik<em1(IMPC)Hmgu>/1810055G02Rik<em1(IMPC)Hmgu>	C57BL/6NCrl-1810055G02Rik<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414763	F	MP:0013278	decreased fasting circulating glucose level	Acadvl<em1(IMPC)H>/Acadvl<em1(IMPC)H>	C57BL/6NTac-Acadvl<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414765	M	MP:0005140	decreased cardiac muscle contractility	Acot12<em1(IMPC)Hmgu>/Acot12<em1(IMPC)Hmgu>	C57BL/6NCrl-Acot12<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414765	M	MP:0002753	dilated heart left ventricle	Acot12<em1(IMPC)Hmgu>/Acot12<em1(IMPC)Hmgu>	C57BL/6NCrl-Acot12<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414766	M	MP:0002965	increased circulating serum albumin level	Acp6<em1(IMPC)Hmgu>/Acp6<+>	C57BL/6NCrl-Acp6<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414767	M	MP:0000745	tremors	Acp6<em1(IMPC)Hmgu>/Acp6<em1(IMPC)Hmgu>	C57BL/6NCrl-Acp6<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414768	M	MP:0002834	decreased heart weight	Acta2<em1(IMPC)H>/Acta2<em1(IMPC)H>	C57BL/6NTac-Acta2<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414769	M	MP:0003961	decreased lean body mass	Agpat5<em1(IMPC)Ccpcz>/Agpat5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Agpat5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414769	M	MP:0001157	small seminal vesicle	Agpat5<em1(IMPC)Ccpcz>/Agpat5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Agpat5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414769	F	MP:0000709	enlarged thymus	Agpat5<em1(IMPC)Ccpcz>/Agpat5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Agpat5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414769	F	MP:0000703	abnormal thymus morphology	Agpat5<em1(IMPC)Ccpcz>/Agpat5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Agpat5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414769	M	MP:0000266	abnormal heart morphology	Agpat5<em1(IMPC)Ccpcz>/Agpat5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Agpat5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414769	M	MP:0002059	abnormal seminal vesicle morphology	Agpat5<em1(IMPC)Ccpcz>/Agpat5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Agpat5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414769	M	MP:0000274	enlarged heart	Agpat5<em1(IMPC)Ccpcz>/Agpat5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Agpat5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414770	F	MP:0000689	abnormal spleen morphology	Agtr1a<em1(IMPC)Rbrc>/Agtr1a<em1(IMPC)Rbrc>	C57BL/6NJcl-Agtr1a<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414770	F	MP:0002596	abnormal hematocrit	Agtr1a<em1(IMPC)Rbrc>/Agtr1a<em1(IMPC)Rbrc>	C57BL/6NJcl-Agtr1a<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414770	F	MP:0001589	abnormal mean corpuscular hemoglobin	Agtr1a<em1(IMPC)Rbrc>/Agtr1a<em1(IMPC)Rbrc>	C57BL/6NJcl-Agtr1a<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414770	F	MP:0001586	abnormal erythrocyte cell number	Agtr1a<em1(IMPC)Rbrc>/Agtr1a<em1(IMPC)Rbrc>	C57BL/6NJcl-Agtr1a<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414770	F	MP:0010066	abnormal red blood cell distribution width	Agtr1a<em1(IMPC)Rbrc>/Agtr1a<em1(IMPC)Rbrc>	C57BL/6NJcl-Agtr1a<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414770	F	MP:0000691	enlarged spleen	Agtr1a<em1(IMPC)Rbrc>/Agtr1a<em1(IMPC)Rbrc>	C57BL/6NJcl-Agtr1a<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414770	F	MP:0004952	increased spleen weight	Agtr1a<em1(IMPC)Rbrc>/Agtr1a<em1(IMPC)Rbrc>	C57BL/6NJcl-Agtr1a<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414770	F	MP:0005563	abnormal hemoglobin content	Agtr1a<em1(IMPC)Rbrc>/Agtr1a<em1(IMPC)Rbrc>	C57BL/6NJcl-Agtr1a<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414773	F	MP:0005343	increased circulating aspartate transaminase level	Aifm3<em1(IMPC)Rbrc>/Aifm3<em1(IMPC)Rbrc>	C57BL/6NJcl-Aifm3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414773	F	MP:0013279	increased fasting circulating glucose level	Aifm3<em1(IMPC)Rbrc>/Aifm3<em1(IMPC)Rbrc>	C57BL/6NJcl-Aifm3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414774	F	MP:0001126	abnormal ovary morphology	Ak7<em1(IMPC)Ccpcz>/Ak7<+>	C57BL/6NCrl-Ak7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414774	M	MP:0000266	abnormal heart morphology	Ak7<em1(IMPC)Ccpcz>/Ak7<+>	C57BL/6NCrl-Ak7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414774	F	MP:0000689	abnormal spleen morphology	Ak7<em1(IMPC)Ccpcz>/Ak7<+>	C57BL/6NCrl-Ak7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414774	M	MP:0001147	small testis	Ak7<em1(IMPC)Ccpcz>/Ak7<+>	C57BL/6NCrl-Ak7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414774	M	MP:0000274	enlarged heart	Ak7<em1(IMPC)Ccpcz>/Ak7<+>	C57BL/6NCrl-Ak7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414774	M	MP:0001146	abnormal testis morphology	Ak7<em1(IMPC)Ccpcz>/Ak7<+>	C57BL/6NCrl-Ak7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414774	F	MP:0002060	abnormal skin morphology	Ak7<em1(IMPC)Ccpcz>/Ak7<+>	C57BL/6NCrl-Ak7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414774	M	MP:0005628	decreased circulating potassium level	Ak7<em1(IMPC)Ccpcz>/Ak7<+>	C57BL/6NCrl-Ak7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414775	M	MP:0002631	abnormal epididymis morphology	Anxa1<em1(IMPC)Ccpcz>/Anxa1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Anxa1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414775	F	MP:0002989	small kidney	Anxa1<em1(IMPC)Ccpcz>/Anxa1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Anxa1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414775	M	MP:0002941	increased circulating alanine transaminase level	Anxa1<em1(IMPC)Ccpcz>/Anxa1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Anxa1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414775	F	MP:0004906	enlarged uterus	Anxa1<em1(IMPC)Ccpcz>/Anxa1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Anxa1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414775	M	MP:0000266	abnormal heart morphology	Anxa1<em1(IMPC)Ccpcz>/Anxa1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Anxa1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414775	F	MP:0000691	enlarged spleen	Anxa1<em1(IMPC)Ccpcz>/Anxa1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Anxa1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414775	F	MP:0004952	increased spleen weight	Anxa1<em1(IMPC)Ccpcz>/Anxa1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Anxa1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414775	F	MP:0010935	increased airway resistance	Anxa1<em1(IMPC)Ccpcz>/Anxa1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Anxa1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414775	F	MP:0004151	decreased circulating iron level	Anxa1<em1(IMPC)Ccpcz>/Anxa1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Anxa1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414775	M	MP:0000692	small spleen	Anxa1<em1(IMPC)Ccpcz>/Anxa1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Anxa1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414775	M	MP:0004931	enlarged epididymis	Anxa1<em1(IMPC)Ccpcz>/Anxa1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Anxa1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414775	F	MP:0001120	abnormal uterus morphology	Anxa1<em1(IMPC)Ccpcz>/Anxa1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Anxa1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414775	M	MP:0000274	enlarged heart	Anxa1<em1(IMPC)Ccpcz>/Anxa1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Anxa1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414776	M	MP:0002135	abnormal kidney morphology	Apcdd1<em1(IMPC)Mbp>/Apcdd1<em1(IMPC)Mbp>	C57BL/6NCrl-Apcdd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414776	M	MP:0002989	small kidney	Apcdd1<em1(IMPC)Mbp>/Apcdd1<em1(IMPC)Mbp>	C57BL/6NCrl-Apcdd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414776	M	MP:0000689	abnormal spleen morphology	Apcdd1<em1(IMPC)Mbp>/Apcdd1<em1(IMPC)Mbp>	C57BL/6NCrl-Apcdd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414776	M	MP:0002060	abnormal skin morphology	Apcdd1<em1(IMPC)Mbp>/Apcdd1<em1(IMPC)Mbp>	C57BL/6NCrl-Apcdd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414776	M	MP:0000691	enlarged spleen	Apcdd1<em1(IMPC)Mbp>/Apcdd1<em1(IMPC)Mbp>	C57BL/6NCrl-Apcdd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414776	F	MP:0002699	abnormal vitreous body morphology	Apcdd1<em1(IMPC)Mbp>/Apcdd1<em1(IMPC)Mbp>	C57BL/6NCrl-Apcdd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414777	M	MP:0000220	increased monocyte cell number	Apobec1<em1(IMPC)Ccpcz>/Apobec1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Apobec1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414777	M	MP:0000266	abnormal heart morphology	Apobec1<em1(IMPC)Ccpcz>/Apobec1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Apobec1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414777	M	MP:0001146	abnormal testis morphology	Apobec1<em1(IMPC)Ccpcz>/Apobec1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Apobec1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414777	F	MP:0002060	abnormal skin morphology	Apobec1<em1(IMPC)Ccpcz>/Apobec1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Apobec1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414777	M	MP:0001147	small testis	Apobec1<em1(IMPC)Ccpcz>/Apobec1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Apobec1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414777	M	MP:0000692	small spleen	Apobec1<em1(IMPC)Ccpcz>/Apobec1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Apobec1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414777	M	MP:0000274	enlarged heart	Apobec1<em1(IMPC)Ccpcz>/Apobec1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Apobec1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414777	F	MP:0001489	decreased startle reflex	Apobec1<em1(IMPC)Ccpcz>/Apobec1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Apobec1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414781	M	MP:0000274	enlarged heart	Arg2<em1(IMPC)Ccpcz>/Arg2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arg2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414781	M	MP:0000692	small spleen	Arg2<em1(IMPC)Ccpcz>/Arg2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arg2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414781	M	MP:0000689	abnormal spleen morphology	Arg2<em1(IMPC)Ccpcz>/Arg2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arg2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414781	F	MP:0000160	kyphosis	Arg2<em1(IMPC)Ccpcz>/Arg2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arg2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414781	F	MP:0000277	abnormal heart shape	Arg2<em1(IMPC)Ccpcz>/Arg2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arg2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414781	F	MP:0001417	decreased exploration in new environment	Arg2<em1(IMPC)Ccpcz>/Arg2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arg2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414781	M	MP:0000709	enlarged thymus	Arg2<em1(IMPC)Ccpcz>/Arg2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arg2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414781	M	MP:0000703	abnormal thymus morphology	Arg2<em1(IMPC)Ccpcz>/Arg2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arg2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414782	M	MP:0002574	increased vertical activity	Arhgef33<em1(IMPC)Tcp>/Arhgef33<em1(IMPC)Tcp>	C57BL/6NCrl-Arhgef33<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414782	F	MP:0001510	abnormal coat appearance	Arhgef33<em1(IMPC)Tcp>/Arhgef33<em1(IMPC)Tcp>	C57BL/6NCrl-Arhgef33<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414782	M	MP:0000745	tremors	Arhgef33<em1(IMPC)Tcp>/Arhgef33<em1(IMPC)Tcp>	C57BL/6NCrl-Arhgef33<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414783	M	MP:0000274	enlarged heart	Atf4<tm1(KOMP)Mbp>/Atf4<+>	C57BL/6NCrl-Atf4<tm1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414783	F	MP:0002941	increased circulating alanine transaminase level	Atf4<tm1(KOMP)Mbp>/Atf4<+>	C57BL/6NCrl-Atf4<tm1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414783	F	MP:0005343	increased circulating aspartate transaminase level	Atf4<tm1(KOMP)Mbp>/Atf4<+>	C57BL/6NCrl-Atf4<tm1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414783	M	MP:0000266	abnormal heart morphology	Atf4<tm1(KOMP)Mbp>/Atf4<+>	C57BL/6NCrl-Atf4<tm1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414785	M	MP:0001304	cataract	Atg14<em1(IMPC)Mbp>/Atg14<+>	C57BL/6NCrl-Atg14<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414785	F	MP:0002060	abnormal skin morphology	Atg14<em1(IMPC)Mbp>/Atg14<+>	C57BL/6NCrl-Atg14<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414785	M	MP:0001146	abnormal testis morphology	Atg14<em1(IMPC)Mbp>/Atg14<+>	C57BL/6NCrl-Atg14<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414785	M	MP:0001148	enlarged testis	Atg14<em1(IMPC)Mbp>/Atg14<+>	C57BL/6NCrl-Atg14<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414785	M	MP:0002699	abnormal vitreous body morphology	Atg14<em1(IMPC)Mbp>/Atg14<+>	C57BL/6NCrl-Atg14<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414787	F	MP:0000709	enlarged thymus	Atp1a1<em1(IMPC)Ccpcz>/Atp1a1<+>	C57BL/6NCrl-Atp1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414787	F	MP:0001120	abnormal uterus morphology	Atp1a1<em1(IMPC)Ccpcz>/Atp1a1<+>	C57BL/6NCrl-Atp1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414787	F	MP:0000702	enlarged lymph nodes	Atp1a1<em1(IMPC)Ccpcz>/Atp1a1<+>	C57BL/6NCrl-Atp1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414787	F	MP:0010579	increased heart left ventricle size	Atp1a1<em1(IMPC)Ccpcz>/Atp1a1<+>	C57BL/6NCrl-Atp1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414787	F	MP:0000703	abnormal thymus morphology	Atp1a1<em1(IMPC)Ccpcz>/Atp1a1<+>	C57BL/6NCrl-Atp1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414787	F	MP:0005564	increased hemoglobin content	Atp1a1<em1(IMPC)Ccpcz>/Atp1a1<+>	C57BL/6NCrl-Atp1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414787	F	MP:0002953	thick ventricular wall	Atp1a1<em1(IMPC)Ccpcz>/Atp1a1<+>	C57BL/6NCrl-Atp1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414787	M	MP:0000274	enlarged heart	Atp1a1<em1(IMPC)Ccpcz>/Atp1a1<+>	C57BL/6NCrl-Atp1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414787	F	MP:0000759	abnormal skeletal muscle morphology	Atp1a1<em1(IMPC)Ccpcz>/Atp1a1<+>	C57BL/6NCrl-Atp1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414787	M	MP:0000266	abnormal heart morphology	Atp1a1<em1(IMPC)Ccpcz>/Atp1a1<+>	C57BL/6NCrl-Atp1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414787	F	MP:0002339	abnormal lymph node morphology	Atp1a1<em1(IMPC)Ccpcz>/Atp1a1<+>	C57BL/6NCrl-Atp1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414791	M	MP:0009142	decreased prepulse inhibition	Aven<em1(IMPC)Hmgu>/Aven<em1(IMPC)Hmgu>	C57BL/6NCrl-Aven<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414792	M	MP:0000702	enlarged lymph nodes	B4galt5<em1(IMPC)Tcp>/B4galt5<+>	C57BL/6NCrl-B4galt5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414792	F	MP:0002060	abnormal skin morphology	B4galt5<em1(IMPC)Tcp>/B4galt5<+>	C57BL/6NCrl-B4galt5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414792	M	MP:0002941	increased circulating alanine transaminase level	B4galt5<em1(IMPC)Tcp>/B4galt5<+>	C57BL/6NCrl-B4galt5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414794	F	MP:0002152	abnormal brain morphology	Bag5<em1(IMPC)Mbp>/Bag5<em1(IMPC)Mbp>	C57BL/6NCrl-Bag5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414794	M	MP:0001304	cataract	Bag5<em1(IMPC)Mbp>/Bag5<em1(IMPC)Mbp>	C57BL/6NCrl-Bag5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414794	F	MP:0002092	abnormal eye morphology	Bag5<em1(IMPC)Mbp>/Bag5<em1(IMPC)Mbp>	C57BL/6NCrl-Bag5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414794	M	MP:0001925	male infertility	Bag5<em1(IMPC)Mbp>/Bag5<em1(IMPC)Mbp>	C57BL/6NCrl-Bag5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414794	F	MP:0001293	anophthalmia	Bag5<em1(IMPC)Mbp>/Bag5<em1(IMPC)Mbp>	C57BL/6NCrl-Bag5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414794	M	MP:0001146	abnormal testis morphology	Bag5<em1(IMPC)Mbp>/Bag5<em1(IMPC)Mbp>	C57BL/6NCrl-Bag5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414794	M	MP:0002699	abnormal vitreous body morphology	Bag5<em1(IMPC)Mbp>/Bag5<em1(IMPC)Mbp>	C57BL/6NCrl-Bag5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414794	M	MP:0001148	enlarged testis	Bag5<em1(IMPC)Mbp>/Bag5<em1(IMPC)Mbp>	C57BL/6NCrl-Bag5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414795	M	MP:0010025	decreased total body fat amount	Bcl2l11<em1(IMPC)H>/Bcl2l11<em1(IMPC)H>	C57BL/6NTac-Bcl2l11<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414795	M	MP:0012362	increased large unstained cell number	Bcl2l11<em1(IMPC)H>/Bcl2l11<em1(IMPC)H>	C57BL/6NTac-Bcl2l11<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414795	F	MP:0005627	increased circulating potassium level	Bcl2l11<em1(IMPC)H>/Bcl2l11<em1(IMPC)H>	C57BL/6NTac-Bcl2l11<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414795	F	MP:0005562	decreased mean corpuscular hemoglobin	Bcl2l11<em1(IMPC)H>/Bcl2l11<em1(IMPC)H>	C57BL/6NTac-Bcl2l11<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414795	F	MP:0010052	increased grip strength	Bcl2l11<em1(IMPC)H>/Bcl2l11<em1(IMPC)H>	C57BL/6NTac-Bcl2l11<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414795	F	MP:0003131	increased erythrocyte cell number	Bcl2l11<em1(IMPC)H>/Bcl2l11<em1(IMPC)H>	C57BL/6NTac-Bcl2l11<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414795	M	MP:0004952	increased spleen weight	Bcl2l11<em1(IMPC)H>/Bcl2l11<em1(IMPC)H>	C57BL/6NTac-Bcl2l11<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414796	M	MP:0002135	abnormal kidney morphology	Bex3<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Bex3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414796	M	MP:0003068	enlarged kidney	Bex3<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Bex3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414796	M	MP:0002060	abnormal skin morphology	Bex3<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Bex3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414796	M	MP:0001304	cataract	Bex3<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Bex3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414796	M	MP:0002699	abnormal vitreous body morphology	Bex3<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Bex3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414797	F	MP:0001297	microphthalmia	Bex3<em1(IMPC)Mbp>/Bex3<em1(IMPC)Mbp>	C57BL/6NCrl-Bex3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414797	F	MP:0001304	cataract	Bex3<em1(IMPC)Mbp>/Bex3<em1(IMPC)Mbp>	C57BL/6NCrl-Bex3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414797	F	MP:0002092	abnormal eye morphology	Bex3<em1(IMPC)Mbp>/Bex3<em1(IMPC)Mbp>	C57BL/6NCrl-Bex3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414797	F	MP:0002060	abnormal skin morphology	Bex3<em1(IMPC)Mbp>/Bex3<em1(IMPC)Mbp>	C57BL/6NCrl-Bex3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414797	F	MP:0002699	abnormal vitreous body morphology	Bex3<em1(IMPC)Mbp>/Bex3<em1(IMPC)Mbp>	C57BL/6NCrl-Bex3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414797	F	MP:0002989	small kidney	Bex3<em1(IMPC)Mbp>/Bex3<em1(IMPC)Mbp>	C57BL/6NCrl-Bex3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414797	F	MP:0002135	abnormal kidney morphology	Bex3<em1(IMPC)Mbp>/Bex3<em1(IMPC)Mbp>	C57BL/6NCrl-Bex3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414798	M	MP:0001925	male infertility	Bicral<em1(IMPC)J>/Bicral<em1(IMPC)J>	C57BL/6NJ-Bicral<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7414798	M	MP:0003961	decreased lean body mass	Bicral<em1(IMPC)J>/Bicral<em1(IMPC)J>	C57BL/6NJ-Bicral<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7414798	M	MP:0010024	increased total body fat amount	Bicral<em1(IMPC)J>/Bicral<em1(IMPC)J>	C57BL/6NJ-Bicral<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7414798	F	MP:0005565	increased blood urea nitrogen level	Bicral<em1(IMPC)J>/Bicral<em1(IMPC)J>	C57BL/6NJ-Bicral<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7414798	M	MP:0000063	decreased bone mineral density	Bicral<em1(IMPC)J>/Bicral<em1(IMPC)J>	C57BL/6NJ-Bicral<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7414798	M	MP:0010124	decreased bone mineral content	Bicral<em1(IMPC)J>/Bicral<em1(IMPC)J>	C57BL/6NJ-Bicral<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7414799	M	MP:0002574	increased vertical activity	Btbd10<em1(IMPC)Hmgu>/Btbd10<em1(IMPC)Hmgu>	C57BL/6NCrl-Btbd10<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414800	M	MP:0001146	abnormal testis morphology	Btbd18<em1(IMPC)Ccpcz>/Btbd18<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414800	M	MP:0000266	abnormal heart morphology	Btbd18<em1(IMPC)Ccpcz>/Btbd18<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414800	M	MP:0001157	small seminal vesicle	Btbd18<em1(IMPC)Ccpcz>/Btbd18<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414800	M	MP:0001147	small testis	Btbd18<em1(IMPC)Ccpcz>/Btbd18<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414800	F	MP:0000709	enlarged thymus	Btbd18<em1(IMPC)Ccpcz>/Btbd18<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414800	F	MP:0000691	enlarged spleen	Btbd18<em1(IMPC)Ccpcz>/Btbd18<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414800	M	MP:0000598	abnormal liver morphology	Btbd18<em1(IMPC)Ccpcz>/Btbd18<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414800	M	MP:0001175	abnormal lung morphology	Btbd18<em1(IMPC)Ccpcz>/Btbd18<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414800	M	MP:0000274	enlarged heart	Btbd18<em1(IMPC)Ccpcz>/Btbd18<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414800	F	MP:0000703	abnormal thymus morphology	Btbd18<em1(IMPC)Ccpcz>/Btbd18<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414800	M	MP:0003641	small lung	Btbd18<em1(IMPC)Ccpcz>/Btbd18<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd18<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	F	MP:0000274	enlarged heart	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	F	MP:0000703	abnormal thymus morphology	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	M	MP:0001297	microphthalmia	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	M	MP:0003961	decreased lean body mass	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	F	MP:0000689	abnormal spleen morphology	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	M	MP:0010895	increased lung compliance	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	F	MP:0009709	hydrometra	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	M	MP:0002059	abnormal seminal vesicle morphology	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	F	MP:0000709	enlarged thymus	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	F	MP:0001120	abnormal uterus morphology	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	F	MP:0000266	abnormal heart morphology	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	F	MP:0002311	abnormal inspiratory capacity	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	F	MP:0001293	anophthalmia	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414801	F	MP:0000691	enlarged spleen	Btbd7<em1(IMPC)Ccpcz>/Btbd7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Btbd7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414802	M	MP:0000221	decreased leukocyte cell number	Btf3<em1(IMPC)Tcp>/Btf3<+>	C57BL/6NCrl-Btf3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414802	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Btf3<em1(IMPC)Tcp>/Btf3<+>	C57BL/6NCrl-Btf3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414802	M	MP:0002092	abnormal eye morphology	Btf3<em1(IMPC)Tcp>/Btf3<+>	C57BL/6NCrl-Btf3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414802	M	MP:0005016	decreased lymphocyte cell number	Btf3<em1(IMPC)Tcp>/Btf3<+>	C57BL/6NCrl-Btf3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414802	M	MP:0000702	enlarged lymph nodes	Btf3<em1(IMPC)Tcp>/Btf3<+>	C57BL/6NCrl-Btf3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414802	M	MP:0011874	enlarged urinary bladder	Btf3<em1(IMPC)Tcp>/Btf3<+>	C57BL/6NCrl-Btf3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414802	M	MP:0010067	increased red blood cell distribution width	Btf3<em1(IMPC)Tcp>/Btf3<+>	C57BL/6NCrl-Btf3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414805	F	MP:0005012	decreased eosinophil cell number	C5ar2<em1(IMPC)H>/C5ar2<em1(IMPC)H>	C57BL/6NTac-C5ar2<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414806	F	MP:0004002	abnormal jejunum morphology	Cadps2<em1(IMPC)Rbrc>/Cadps2<em1(IMPC)Rbrc>	C57BL/6NJcl-Cadps2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414806	F	MP:0000202	abnormal circulating alkaline phosphatase level	Cadps2<em1(IMPC)Rbrc>/Cadps2<em1(IMPC)Rbrc>	C57BL/6NJcl-Cadps2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414806	F	MP:0003271	abnormal duodenum morphology	Cadps2<em1(IMPC)Rbrc>/Cadps2<em1(IMPC)Rbrc>	C57BL/6NJcl-Cadps2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414806	F	MP:0002581	abnormal ileum morphology	Cadps2<em1(IMPC)Rbrc>/Cadps2<em1(IMPC)Rbrc>	C57BL/6NJcl-Cadps2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414807	F	MP:0001562	abnormal circulating calcium level	Calcr<em1(IMPC)Rbrc>/Calcr<em1(IMPC)Rbrc>	C57BL/6NJcl-Calcr<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414807	F	MP:0000202	abnormal circulating alkaline phosphatase level	Calcr<em1(IMPC)Rbrc>/Calcr<em1(IMPC)Rbrc>	C57BL/6NJcl-Calcr<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414808	F	MP:0002111	abnormal tail morphology	Capza1<em1(IMPC)Tcp>/Capza1<em1(IMPC)Tcp>	C57BL/6NCrl-Capza1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414808	M	MP:0000208	decreased hematocrit	Capza1<em1(IMPC)Tcp>/Capza1<em1(IMPC)Tcp>	C57BL/6NCrl-Capza1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414808	M	MP:0002591	decreased mean corpuscular volume	Capza1<em1(IMPC)Tcp>/Capza1<em1(IMPC)Tcp>	C57BL/6NCrl-Capza1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414808	M	MP:0001304	cataract	Capza1<em1(IMPC)Tcp>/Capza1<em1(IMPC)Tcp>	C57BL/6NCrl-Capza1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414808	M	MP:0020870	decreased thigmotaxis	Capza1<em1(IMPC)Tcp>/Capza1<em1(IMPC)Tcp>	C57BL/6NCrl-Capza1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414808	F	MP:0000220	increased monocyte cell number	Capza1<em1(IMPC)Tcp>/Capza1<em1(IMPC)Tcp>	C57BL/6NCrl-Capza1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414808	M	MP:0000221	decreased leukocyte cell number	Capza1<em1(IMPC)Tcp>/Capza1<em1(IMPC)Tcp>	C57BL/6NCrl-Capza1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414808	M	MP:0005016	decreased lymphocyte cell number	Capza1<em1(IMPC)Tcp>/Capza1<em1(IMPC)Tcp>	C57BL/6NCrl-Capza1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414809	F	MP:0001402	decreased locomotor activity	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	M	MP:0001147	small testis	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	M	MP:0000692	small spleen	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	F	MP:0000218	increased leukocyte cell number	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	F	MP:0001120	abnormal uterus morphology	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	F	MP:0009709	hydrometra	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	M	MP:0000689	abnormal spleen morphology	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	F	MP:0005013	increased lymphocyte cell number	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	F	MP:0000709	enlarged thymus	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	M	MP:0008074	increased CD4-positive, alpha-beta T cell number	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	F	MP:0020421	increased freezing behavior	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	M	MP:0001146	abnormal testis morphology	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	F	MP:0000703	abnormal thymus morphology	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	M	MP:0013763	increased T-helper cell number	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414809	M	MP:0002966	decreased circulating alkaline phosphatase level	Card11<em1(IMPC)Ccpcz>/Card11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Card11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414810	F	MP:0005238	increased brain size	Casp2<em1(IMPC)Mbp>/Casp2<em1(IMPC)Mbp>	C57BL/6NCrl-Casp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414810	M	MP:0001289	persistence of hyaloid vascular system	Casp2<em1(IMPC)Mbp>/Casp2<em1(IMPC)Mbp>	C57BL/6NCrl-Casp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414810	M	MP:0001148	enlarged testis	Casp2<em1(IMPC)Mbp>/Casp2<em1(IMPC)Mbp>	C57BL/6NCrl-Casp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414810	F	MP:0002699	abnormal vitreous body morphology	Casp2<em1(IMPC)Mbp>/Casp2<em1(IMPC)Mbp>	C57BL/6NCrl-Casp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414810	M	MP:0001146	abnormal testis morphology	Casp2<em1(IMPC)Mbp>/Casp2<em1(IMPC)Mbp>	C57BL/6NCrl-Casp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414810	F	MP:0000494	abnormal cecum morphology	Casp2<em1(IMPC)Mbp>/Casp2<em1(IMPC)Mbp>	C57BL/6NCrl-Casp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414810	F	MP:0002060	abnormal skin morphology	Casp2<em1(IMPC)Mbp>/Casp2<em1(IMPC)Mbp>	C57BL/6NCrl-Casp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414810	F	MP:0009476	enlarged cecum	Casp2<em1(IMPC)Mbp>/Casp2<em1(IMPC)Mbp>	C57BL/6NCrl-Casp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414810	F	MP:0002152	abnormal brain morphology	Casp2<em1(IMPC)Mbp>/Casp2<em1(IMPC)Mbp>	C57BL/6NCrl-Casp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414810	F	MP:0002135	abnormal kidney morphology	Casp2<em1(IMPC)Mbp>/Casp2<em1(IMPC)Mbp>	C57BL/6NCrl-Casp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414810	F	MP:0002989	small kidney	Casp2<em1(IMPC)Mbp>/Casp2<em1(IMPC)Mbp>	C57BL/6NCrl-Casp2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414811	M	MP:0000062	increased bone mineral density	Cbr4<em1(IMPC)Bay>/Cbr4<+>	C57BL/6N-Cbr4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414813	F	MP:0002092	abnormal eye morphology	Ccbe1<em1(IMPC)Mbp>/Ccbe1<+>	C57BL/6NCrl-Ccbe1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414813	F	MP:0004906	enlarged uterus	Ccbe1<em1(IMPC)Mbp>/Ccbe1<+>	C57BL/6NCrl-Ccbe1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414813	M	MP:0002792	abnormal retina vasculature morphology	Ccbe1<em1(IMPC)Mbp>/Ccbe1<+>	C57BL/6NCrl-Ccbe1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414813	F	MP:0000601	small liver	Ccbe1<em1(IMPC)Mbp>/Ccbe1<+>	C57BL/6NCrl-Ccbe1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414813	F	MP:0001120	abnormal uterus morphology	Ccbe1<em1(IMPC)Mbp>/Ccbe1<+>	C57BL/6NCrl-Ccbe1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414813	F	MP:0000598	abnormal liver morphology	Ccbe1<em1(IMPC)Mbp>/Ccbe1<+>	C57BL/6NCrl-Ccbe1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414815	F	MP:0002092	abnormal eye morphology	Ccdc198<em1(IMPC)Ccpcz>/Ccdc198<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccdc198<em1(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:7414815	F	MP:0001297	microphthalmia	Ccdc198<em1(IMPC)Ccpcz>/Ccdc198<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccdc198<em1(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:7414815	M	MP:0002631	abnormal epididymis morphology	Ccdc198<em1(IMPC)Ccpcz>/Ccdc198<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccdc198<em1(IMPC)Ccpcz>/Ph	N	MGI:5576271
MGI:7414816	M	MP:0000062	increased bone mineral density	Ccdc92<tm1a(KOMP)Mbp>/Ccdc92<tm1a(KOMP)Mbp>	C57BL/6NCrl-Ccdc92<tm1a(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414816	F	MP:0000266	abnormal heart morphology	Ccdc92<tm1a(KOMP)Mbp>/Ccdc92<tm1a(KOMP)Mbp>	C57BL/6NCrl-Ccdc92<tm1a(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414816	F	MP:0000274	enlarged heart	Ccdc92<tm1a(KOMP)Mbp>/Ccdc92<tm1a(KOMP)Mbp>	C57BL/6NCrl-Ccdc92<tm1a(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414816	M	MP:0002965	increased circulating serum albumin level	Ccdc92<tm1a(KOMP)Mbp>/Ccdc92<tm1a(KOMP)Mbp>	C57BL/6NCrl-Ccdc92<tm1a(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414816	M	MP:0005565	increased blood urea nitrogen level	Ccdc92<tm1a(KOMP)Mbp>/Ccdc92<tm1a(KOMP)Mbp>	C57BL/6NCrl-Ccdc92<tm1a(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414817	M	MP:0000274	enlarged heart	Ccl28<em1(IMPC)Ccpcz>/Ccl28<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccl28<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414817	F	MP:0009709	hydrometra	Ccl28<em1(IMPC)Ccpcz>/Ccl28<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccl28<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414817	F	MP:0001120	abnormal uterus morphology	Ccl28<em1(IMPC)Ccpcz>/Ccl28<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccl28<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414817	F	MP:0000598	abnormal liver morphology	Ccl28<em1(IMPC)Ccpcz>/Ccl28<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccl28<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414817	F	MP:0000689	abnormal spleen morphology	Ccl28<em1(IMPC)Ccpcz>/Ccl28<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccl28<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414817	M	MP:0002092	abnormal eye morphology	Ccl28<em1(IMPC)Ccpcz>/Ccl28<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccl28<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414817	F	MP:0000691	enlarged spleen	Ccl28<em1(IMPC)Ccpcz>/Ccl28<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccl28<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414817	F	MP:0002941	increased circulating alanine transaminase level	Ccl28<em1(IMPC)Ccpcz>/Ccl28<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccl28<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414817	M	MP:0000266	abnormal heart morphology	Ccl28<em1(IMPC)Ccpcz>/Ccl28<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccl28<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414818	F	MP:0000709	enlarged thymus	Ccr3<em1(IMPC)Ccpcz>/Ccr3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccr3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414818	M	MP:0000266	abnormal heart morphology	Ccr3<em1(IMPC)Ccpcz>/Ccr3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccr3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414818	M	MP:0000274	enlarged heart	Ccr3<em1(IMPC)Ccpcz>/Ccr3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccr3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414818	F	MP:0001312	abnormal cornea morphology	Ccr3<em1(IMPC)Ccpcz>/Ccr3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccr3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414818	F	MP:0000703	abnormal thymus morphology	Ccr3<em1(IMPC)Ccpcz>/Ccr3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccr3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414818	F	MP:0002110	abnormal digit morphology	Ccr3<em1(IMPC)Ccpcz>/Ccr3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccr3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414819	M	MP:0008044	increased NK cell number	Cd38<em1(IMPC)Ccpcz>/Cd38<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414819	F	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Cd38<em1(IMPC)Ccpcz>/Cd38<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414819	F	MP:0000703	abnormal thymus morphology	Cd38<em1(IMPC)Ccpcz>/Cd38<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414819	F	MP:0000709	enlarged thymus	Cd38<em1(IMPC)Ccpcz>/Cd38<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd38<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414821	F	MP:0000195	decreased circulating calcium level	Cdh18<em1(IMPC)J>/Cdh18<em1(IMPC)J>	C57BL/6NJ-Cdh18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7414821	F	MP:0001417	decreased exploration in new environment	Cdh18<em1(IMPC)J>/Cdh18<em1(IMPC)J>	C57BL/6NJ-Cdh18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7414822	F	MP:0001402	decreased locomotor activity	Cenpx<em1(IMPC)Bay>/Cenpx<em1(IMPC)Bay>	C57BL/6N-Cenpx<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414823	M	MP:0001489	decreased startle reflex	Cep170b<em1(IMPC)Hmgu>/Cep170b<em1(IMPC)Hmgu>	C57BL/6NCrl-Cep170b<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414824	M	MP:0000627	abnormal mammary gland morphology	Cfap161<em1(IMPC)Ccpcz>/Cfap161<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cfap161<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414824	M	MP:0005355	enlarged thyroid gland	Cfap161<em1(IMPC)Ccpcz>/Cfap161<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cfap161<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414824	F	MP:0000452	abnormal mouth morphology	Cfap161<em1(IMPC)Ccpcz>/Cfap161<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cfap161<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414824	M	MP:0000681	abnormal thyroid gland morphology	Cfap161<em1(IMPC)Ccpcz>/Cfap161<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cfap161<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414824	F	MP:0000689	abnormal spleen morphology	Cfap161<em1(IMPC)Ccpcz>/Cfap161<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cfap161<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414824	F	MP:0000691	enlarged spleen	Cfap161<em1(IMPC)Ccpcz>/Cfap161<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cfap161<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414826	F	MP:0000691	enlarged spleen	Champ1<em1(IMPC)Mbp>/Champ1<+>	C57BL/6NCrl-Champ1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414826	M	MP:0000692	small spleen	Champ1<em1(IMPC)Mbp>/Champ1<+>	C57BL/6NCrl-Champ1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414827	M	MP:0000428	abnormal craniofacial morphology	Champ1<em1(IMPC)Mbp>/Champ1<em1(IMPC)Mbp>	C57BL/6NCrl-Champ1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414828	M	MP:0001148	enlarged testis	Chchd2<em1(IMPC)Mbp>/Chchd2<em1(IMPC)Mbp>	C57BL/6NCrl-Chchd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414828	M	MP:0001146	abnormal testis morphology	Chchd2<em1(IMPC)Mbp>/Chchd2<em1(IMPC)Mbp>	C57BL/6NCrl-Chchd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414828	F	MP:0002060	abnormal skin morphology	Chchd2<em1(IMPC)Mbp>/Chchd2<em1(IMPC)Mbp>	C57BL/6NCrl-Chchd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414828	M	MP:0001304	cataract	Chchd2<em1(IMPC)Mbp>/Chchd2<em1(IMPC)Mbp>	C57BL/6NCrl-Chchd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414828	F	MP:0000598	abnormal liver morphology	Chchd2<em1(IMPC)Mbp>/Chchd2<em1(IMPC)Mbp>	C57BL/6NCrl-Chchd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414828	F	MP:0000601	small liver	Chchd2<em1(IMPC)Mbp>/Chchd2<em1(IMPC)Mbp>	C57BL/6NCrl-Chchd2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414829	M	MP:0002135	abnormal kidney morphology	Chd5<em1(IMPC)Mbp>/Chd5<em1(IMPC)Mbp>	C57BL/6NCrl-Chd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414829	M	MP:0009552	urinary bladder obstruction	Chd5<em1(IMPC)Mbp>/Chd5<em1(IMPC)Mbp>	C57BL/6NCrl-Chd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414829	M	MP:0003068	enlarged kidney	Chd5<em1(IMPC)Mbp>/Chd5<em1(IMPC)Mbp>	C57BL/6NCrl-Chd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414830	F	MP:0001697	abnormal embryo size	Chp1<em1(IMPC)Tcp>/Chp1<+>	C57BL/6NCrl-Chp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414830	F	MP:0003984	embryonic growth retardation	Chp1<em1(IMPC)Tcp>/Chp1<+>	C57BL/6NCrl-Chp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414830	F	MP:0000367	abnormal coat/ hair morphology	Chp1<em1(IMPC)Tcp>/Chp1<+>	C57BL/6NCrl-Chp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414832	F	MP:0004924	abnormal behavior	Chst10<em1(IMPC)Hmgu>/Chst10<em1(IMPC)Hmgu>	C57BL/6NCrl-Chst10<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414832	F	MP:0020870	decreased thigmotaxis	Chst10<em1(IMPC)Hmgu>/Chst10<em1(IMPC)Hmgu>	C57BL/6NCrl-Chst10<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414832	M	MP:0010067	increased red blood cell distribution width	Chst10<em1(IMPC)Hmgu>/Chst10<em1(IMPC)Hmgu>	C57BL/6NCrl-Chst10<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414832	F	MP:0001364	decreased anxiety-related response	Chst10<em1(IMPC)Hmgu>/Chst10<em1(IMPC)Hmgu>	C57BL/6NCrl-Chst10<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414832	F	MP:0001402	decreased locomotor activity	Chst10<em1(IMPC)Hmgu>/Chst10<em1(IMPC)Hmgu>	C57BL/6NCrl-Chst10<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414832	F	MP:0011965	decreased total retina thickness	Chst10<em1(IMPC)Hmgu>/Chst10<em1(IMPC)Hmgu>	C57BL/6NCrl-Chst10<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414832	M	MP:0004952	increased spleen weight	Chst10<em1(IMPC)Hmgu>/Chst10<em1(IMPC)Hmgu>	C57BL/6NCrl-Chst10<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414833	F	MP:0000702	enlarged lymph nodes	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	M	MP:0009476	enlarged cecum	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	M	MP:0010053	decreased grip strength	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	F	MP:0003795	abnormal bone structure	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	M	MP:0009552	urinary bladder obstruction	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	F	MP:0000689	abnormal spleen morphology	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	F	MP:0000691	enlarged spleen	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	F	MP:0001304	cataract	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	F	MP:0002339	abnormal lymph node morphology	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	F	MP:0002699	abnormal vitreous body morphology	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	M	MP:0000598	abnormal liver morphology	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	M	MP:0000494	abnormal cecum morphology	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	M	MP:0000774	decreased brain size	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	F	MP:0001314	cornea opacity	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	F	MP:0002060	abnormal skin morphology	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414833	M	MP:0000601	small liver	Chsy1<em1(IMPC)Mbp>/Chsy1<em1(IMPC)Mbp>	C57BL/6NCrl-Chsy1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414834	F	MP:0000703	abnormal thymus morphology	Chuk<em1(IMPC)Ccpcz>/Chuk<+>	C57BL/6NCrl-Chuk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414834	M	MP:0001146	abnormal testis morphology	Chuk<em1(IMPC)Ccpcz>/Chuk<+>	C57BL/6NCrl-Chuk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414834	F	MP:0002092	abnormal eye morphology	Chuk<em1(IMPC)Ccpcz>/Chuk<+>	C57BL/6NCrl-Chuk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414834	M	MP:0002100	abnormal tooth morphology	Chuk<em1(IMPC)Ccpcz>/Chuk<+>	C57BL/6NCrl-Chuk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414834	F	MP:0001120	abnormal uterus morphology	Chuk<em1(IMPC)Ccpcz>/Chuk<+>	C57BL/6NCrl-Chuk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414834	F	MP:0009709	hydrometra	Chuk<em1(IMPC)Ccpcz>/Chuk<+>	C57BL/6NCrl-Chuk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414834	M	MP:0002339	abnormal lymph node morphology	Chuk<em1(IMPC)Ccpcz>/Chuk<+>	C57BL/6NCrl-Chuk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414834	M	MP:0013129	abnormal tooth color	Chuk<em1(IMPC)Ccpcz>/Chuk<+>	C57BL/6NCrl-Chuk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414834	F	MP:0000709	enlarged thymus	Chuk<em1(IMPC)Ccpcz>/Chuk<+>	C57BL/6NCrl-Chuk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414834	F	MP:0001297	microphthalmia	Chuk<em1(IMPC)Ccpcz>/Chuk<+>	C57BL/6NCrl-Chuk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414834	M	MP:0001147	small testis	Chuk<em1(IMPC)Ccpcz>/Chuk<+>	C57BL/6NCrl-Chuk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414834	M	MP:0000702	enlarged lymph nodes	Chuk<em1(IMPC)Ccpcz>/Chuk<+>	C57BL/6NCrl-Chuk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414836	F	MP:0002989	small kidney	Clca2<em1(IMPC)Mbp>/Clca2<em1(IMPC)Mbp>	C57BL/6NCrl-Clca2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414836	F	MP:0002135	abnormal kidney morphology	Clca2<em1(IMPC)Mbp>/Clca2<em1(IMPC)Mbp>	C57BL/6NCrl-Clca2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414836	M	MP:0001146	abnormal testis morphology	Clca2<em1(IMPC)Mbp>/Clca2<em1(IMPC)Mbp>	C57BL/6NCrl-Clca2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414836	M	MP:0001147	small testis	Clca2<em1(IMPC)Mbp>/Clca2<em1(IMPC)Mbp>	C57BL/6NCrl-Clca2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414836	F	MP:0002941	increased circulating alanine transaminase level	Clca2<em1(IMPC)Mbp>/Clca2<em1(IMPC)Mbp>	C57BL/6NCrl-Clca2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414836	M	MP:0001304	cataract	Clca2<em1(IMPC)Mbp>/Clca2<em1(IMPC)Mbp>	C57BL/6NCrl-Clca2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414836	M	MP:0001325	abnormal retina morphology	Clca2<em1(IMPC)Mbp>/Clca2<em1(IMPC)Mbp>	C57BL/6NCrl-Clca2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414837	M	MP:0002606	increased basophil cell number	Cldn9<em1(IMPC)H>/Cldn9<em1(IMPC)H>	C57BL/6NTac-Cldn9<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414838	M	MP:0003604	single kidney	Clnk<em1(IMPC)Ccpcz>/Clnk<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clnk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414838	F	MP:0000709	enlarged thymus	Clnk<em1(IMPC)Ccpcz>/Clnk<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clnk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414838	F	MP:0000703	abnormal thymus morphology	Clnk<em1(IMPC)Ccpcz>/Clnk<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clnk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414838	M	MP:0002060	abnormal skin morphology	Clnk<em1(IMPC)Ccpcz>/Clnk<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clnk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414838	M	MP:0000266	abnormal heart morphology	Clnk<em1(IMPC)Ccpcz>/Clnk<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clnk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414838	M	MP:0000691	enlarged spleen	Clnk<em1(IMPC)Ccpcz>/Clnk<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clnk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414838	F	MP:0004819	decreased skeletal muscle mass	Clnk<em1(IMPC)Ccpcz>/Clnk<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clnk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414838	M	MP:0000274	enlarged heart	Clnk<em1(IMPC)Ccpcz>/Clnk<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clnk<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414839	M	MP:0001417	decreased exploration in new environment	Clptm1<em1(IMPC)Tcp>/Clptm1<+>	C57BL/6NCrl-Clptm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414839	M	MP:0000220	increased monocyte cell number	Clptm1<em1(IMPC)Tcp>/Clptm1<+>	C57BL/6NCrl-Clptm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414839	M	MP:0001402	decreased locomotor activity	Clptm1<em1(IMPC)Tcp>/Clptm1<+>	C57BL/6NCrl-Clptm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414839	M	MP:0002060	abnormal skin morphology	Clptm1<em1(IMPC)Tcp>/Clptm1<+>	C57BL/6NCrl-Clptm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414839	M	MP:0000702	enlarged lymph nodes	Clptm1<em1(IMPC)Tcp>/Clptm1<+>	C57BL/6NCrl-Clptm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414839	F	MP:0000208	decreased hematocrit	Clptm1<em1(IMPC)Tcp>/Clptm1<+>	C57BL/6NCrl-Clptm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414839	M	MP:0001363	increased anxiety-related response	Clptm1<em1(IMPC)Tcp>/Clptm1<+>	C57BL/6NCrl-Clptm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414839	M	MP:0001488	increased startle reflex	Clptm1<em1(IMPC)Tcp>/Clptm1<+>	C57BL/6NCrl-Clptm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414841	M	MP:0020870	decreased thigmotaxis	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0000266	abnormal heart morphology	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0004924	abnormal behavior	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0001364	decreased anxiety-related response	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	F	MP:0001127	small ovary	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0010025	decreased total body fat amount	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0003068	enlarged kidney	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0003960	increased lean body mass	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0002135	abnormal kidney morphology	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0001147	small testis	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	F	MP:0001126	abnormal ovary morphology	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0010123	increased bone mineral content	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0000274	enlarged heart	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0001925	male infertility	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0000598	abnormal liver morphology	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0001146	abnormal testis morphology	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414841	M	MP:0010067	increased red blood cell distribution width	Cnot7<em1(IMPC)Rbrc>/Cnot7<em1(IMPC)Rbrc>	C57BL/6NJcl-Cnot7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414843	M	MP:0011100	preweaning lethality, complete penetrance	Coa8<em1(IMPC)Bay>/Coa8<em1(IMPC)Bay>	C57BL/6N-Coa8<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414844	M	MP:0000219	increased neutrophil cell number	Coasy<em1(IMPC)H>/Coasy<+>	C57BL/6NTac-Coasy<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414844	F	MP:0002599	increased mean platelet volume	Coasy<em1(IMPC)H>/Coasy<+>	C57BL/6NTac-Coasy<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414844	F	MP:0005627	increased circulating potassium level	Coasy<em1(IMPC)H>/Coasy<+>	C57BL/6NTac-Coasy<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414845	M	MP:0005562	decreased mean corpuscular hemoglobin	Cplx4<em1(IMPC)H>/Cplx4<em1(IMPC)H>	C57BL/6NTac-Cplx4<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414846	F	MP:0002135	abnormal kidney morphology	Crmp1<em1(IMPC)Mbp>/Crmp1<em1(IMPC)Mbp>	C57BL/6NCrl-Crmp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414846	M	MP:0002060	abnormal skin morphology	Crmp1<em1(IMPC)Mbp>/Crmp1<em1(IMPC)Mbp>	C57BL/6NCrl-Crmp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414846	M	MP:0001304	cataract	Crmp1<em1(IMPC)Mbp>/Crmp1<em1(IMPC)Mbp>	C57BL/6NCrl-Crmp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414846	F	MP:0002989	small kidney	Crmp1<em1(IMPC)Mbp>/Crmp1<em1(IMPC)Mbp>	C57BL/6NCrl-Crmp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414847	F	MP:0005016	decreased lymphocyte cell number	Crppa<em1(IMPC)H>/Crppa<+>	C57BL/6NTac-Crppa<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414847	F	MP:0002599	increased mean platelet volume	Crppa<em1(IMPC)H>/Crppa<+>	C57BL/6NTac-Crppa<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414847	M	MP:0000219	increased neutrophil cell number	Crppa<em1(IMPC)H>/Crppa<+>	C57BL/6NTac-Crppa<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414849	M	MP:0002608	increased hematocrit	Ctss<em1(IMPC)H>/Ctss<em1(IMPC)H>	C57BL/6NTac-Ctss<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414850	M	MP:0000218	increased leukocyte cell number	Cxcl13<em2(IMPC)H>/Cxcl13<em2(IMPC)H>	C57BL/6NTac-Cxcl13<em2(IMPC)H>/H	N	MGI:5576271
MGI:7414850	M	MP:0002606	increased basophil cell number	Cxcl13<em2(IMPC)H>/Cxcl13<em2(IMPC)H>	C57BL/6NTac-Cxcl13<em2(IMPC)H>/H	N	MGI:5576271
MGI:7414850	M	MP:0010067	increased red blood cell distribution width	Cxcl13<em2(IMPC)H>/Cxcl13<em2(IMPC)H>	C57BL/6NTac-Cxcl13<em2(IMPC)H>/H	N	MGI:5576271
MGI:7414850	M	MP:0005013	increased lymphocyte cell number	Cxcl13<em2(IMPC)H>/Cxcl13<em2(IMPC)H>	C57BL/6NTac-Cxcl13<em2(IMPC)H>/H	N	MGI:5576271
MGI:7414851	M	MP:0001304	cataract	Cxcr4<em1(IMPC)Mbp>/Cxcr4<+>	C57BL/6NCrl-Cxcr4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414851	M	MP:0002135	abnormal kidney morphology	Cxcr4<em1(IMPC)Mbp>/Cxcr4<+>	C57BL/6NCrl-Cxcr4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414851	M	MP:0003068	enlarged kidney	Cxcr4<em1(IMPC)Mbp>/Cxcr4<+>	C57BL/6NCrl-Cxcr4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414851	M	MP:0000218	increased leukocyte cell number	Cxcr4<em1(IMPC)Mbp>/Cxcr4<+>	C57BL/6NCrl-Cxcr4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414851	F	MP:0002060	abnormal skin morphology	Cxcr4<em1(IMPC)Mbp>/Cxcr4<+>	C57BL/6NCrl-Cxcr4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414851	M	MP:0002699	abnormal vitreous body morphology	Cxcr4<em1(IMPC)Mbp>/Cxcr4<+>	C57BL/6NCrl-Cxcr4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414851	F	MP:0001340	abnormal eyelid morphology	Cxcr4<em1(IMPC)Mbp>/Cxcr4<+>	C57BL/6NCrl-Cxcr4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414851	F	MP:0005554	decreased circulating creatinine level	Cxcr4<em1(IMPC)Mbp>/Cxcr4<+>	C57BL/6NCrl-Cxcr4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414851	M	MP:0000689	abnormal spleen morphology	Cxcr4<em1(IMPC)Mbp>/Cxcr4<+>	C57BL/6NCrl-Cxcr4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414851	M	MP:0001148	enlarged testis	Cxcr4<em1(IMPC)Mbp>/Cxcr4<+>	C57BL/6NCrl-Cxcr4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414851	M	MP:0001146	abnormal testis morphology	Cxcr4<em1(IMPC)Mbp>/Cxcr4<+>	C57BL/6NCrl-Cxcr4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414851	M	MP:0005013	increased lymphocyte cell number	Cxcr4<em1(IMPC)Mbp>/Cxcr4<+>	C57BL/6NCrl-Cxcr4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414851	M	MP:0000691	enlarged spleen	Cxcr4<em1(IMPC)Mbp>/Cxcr4<+>	C57BL/6NCrl-Cxcr4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414853	F	MP:0010123	increased bone mineral content	Cyp2c38<em1(IMPC)Bay>/Cyp2c38<+>	C57BL/6N-Cyp2c38<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414853	F	MP:0003795	abnormal bone structure	Cyp2c38<em1(IMPC)Bay>/Cyp2c38<+>	C57BL/6N-Cyp2c38<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414855	F	MP:0005554	decreased circulating creatinine level	Cyria<em1(IMPC)Hmgu>/Cyria<em1(IMPC)Hmgu>	C57BL/6NCrl-Cyria<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414855	F	MP:0010097	abnormal retina blood vessel morphology	Cyria<em1(IMPC)Hmgu>/Cyria<em1(IMPC)Hmgu>	C57BL/6NCrl-Cyria<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414856	F	MP:0003731	abnormal retina outer nuclear layer morphology	Dazap2<em1(IMPC)Bay>/Dazap2<em1(IMPC)Bay>	C57BL/6N-Dazap2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414856	F	MP:0003733	abnormal retina inner nuclear layer morphology	Dazap2<em1(IMPC)Bay>/Dazap2<em1(IMPC)Bay>	C57BL/6N-Dazap2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414857	M	MP:0000598	abnormal liver morphology	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6NCrl-Dbn1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:7414857	M	MP:0000266	abnormal heart morphology	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6NCrl-Dbn1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:7414857	M	MP:0000274	enlarged heart	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6NCrl-Dbn1<tm1b(KOMP)Wtsi>/Wtsi	N	MGI:5576271
MGI:7414859	M	MP:0000691	enlarged spleen	Dennd10<em1(IMPC)Ccpcz>/Dennd10<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dennd10<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414859	F	MP:0002764	short tibia	Dennd10<em1(IMPC)Ccpcz>/Dennd10<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dennd10<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414859	M	MP:0000274	enlarged heart	Dennd10<em1(IMPC)Ccpcz>/Dennd10<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dennd10<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414859	M	MP:0000266	abnormal heart morphology	Dennd10<em1(IMPC)Ccpcz>/Dennd10<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dennd10<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414860	F	MP:0011886	increased circulating lipase level	Dennd6b<em1(IMPC)Hmgu>/Dennd6b<em1(IMPC)Hmgu>	C57BL/6NCrl-Dennd6b<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414862	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Dhx15<em1(IMPC)Tcp>/Dhx15<+>	C57BL/6NCrl-Dhx15<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414862	M	MP:0003131	increased erythrocyte cell number	Dhx15<em1(IMPC)Tcp>/Dhx15<+>	C57BL/6NCrl-Dhx15<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414862	M	MP:0009142	decreased prepulse inhibition	Dhx15<em1(IMPC)Tcp>/Dhx15<+>	C57BL/6NCrl-Dhx15<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414862	F	MP:0000208	decreased hematocrit	Dhx15<em1(IMPC)Tcp>/Dhx15<+>	C57BL/6NCrl-Dhx15<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414862	F	MP:0003900	shortened QT interval	Dhx15<em1(IMPC)Tcp>/Dhx15<+>	C57BL/6NCrl-Dhx15<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414865	M	MP:0001146	abnormal testis morphology	Dnase1l3<em1(IMPC)Mbp>/Dnase1l3<em1(IMPC)Mbp>	C57BL/6NCrl-Dnase1l3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414865	F	MP:0000601	small liver	Dnase1l3<em1(IMPC)Mbp>/Dnase1l3<em1(IMPC)Mbp>	C57BL/6NCrl-Dnase1l3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414865	F	MP:0004952	increased spleen weight	Dnase1l3<em1(IMPC)Mbp>/Dnase1l3<em1(IMPC)Mbp>	C57BL/6NCrl-Dnase1l3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414865	F	MP:0001297	microphthalmia	Dnase1l3<em1(IMPC)Mbp>/Dnase1l3<em1(IMPC)Mbp>	C57BL/6NCrl-Dnase1l3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414865	F	MP:0000598	abnormal liver morphology	Dnase1l3<em1(IMPC)Mbp>/Dnase1l3<em1(IMPC)Mbp>	C57BL/6NCrl-Dnase1l3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414865	F	MP:0002092	abnormal eye morphology	Dnase1l3<em1(IMPC)Mbp>/Dnase1l3<em1(IMPC)Mbp>	C57BL/6NCrl-Dnase1l3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414865	M	MP:0001148	enlarged testis	Dnase1l3<em1(IMPC)Mbp>/Dnase1l3<em1(IMPC)Mbp>	C57BL/6NCrl-Dnase1l3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414866	M	MP:0001486	abnormal startle reflex	Dock4<em1(IMPC)Hmgu>/Dock4<em1(IMPC)Hmgu>	C57BL/6NCrl-Dock4<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414866	F	MP:0004924	abnormal behavior	Dock4<em1(IMPC)Hmgu>/Dock4<em1(IMPC)Hmgu>	C57BL/6NCrl-Dock4<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414866	F	MP:0004906	enlarged uterus	Dock4<em1(IMPC)Hmgu>/Dock4<em1(IMPC)Hmgu>	C57BL/6NCrl-Dock4<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414866	F	MP:0020870	decreased thigmotaxis	Dock4<em1(IMPC)Hmgu>/Dock4<em1(IMPC)Hmgu>	C57BL/6NCrl-Dock4<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414866	F	MP:0001364	decreased anxiety-related response	Dock4<em1(IMPC)Hmgu>/Dock4<em1(IMPC)Hmgu>	C57BL/6NCrl-Dock4<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414867	M	MP:0001925	male infertility	Drc1<em1(IMPC)Bay>/Drc1<em1(IMPC)Bay>	C57BL/6N-Drc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414868	F	MP:0000613	abnormal salivary gland morphology	Drg1<em1(IMPC)Tcp>/Drg1<+>	C57BL/6NCrl-Drg1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414868	M	MP:0002060	abnormal skin morphology	Drg1<em1(IMPC)Tcp>/Drg1<+>	C57BL/6NCrl-Drg1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414868	M	MP:0010067	increased red blood cell distribution width	Drg1<em1(IMPC)Tcp>/Drg1<+>	C57BL/6NCrl-Drg1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414871	M	MP:0001417	decreased exploration in new environment	Ebna1bp2<em1(IMPC)Tcp>/Ebna1bp2<+>	C57BL/6NCrl-Ebna1bp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414871	F	MP:0005562	decreased mean corpuscular hemoglobin	Ebna1bp2<em1(IMPC)Tcp>/Ebna1bp2<+>	C57BL/6NCrl-Ebna1bp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414871	M	MP:0000691	enlarged spleen	Ebna1bp2<em1(IMPC)Tcp>/Ebna1bp2<+>	C57BL/6NCrl-Ebna1bp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414871	M	MP:0003068	enlarged kidney	Ebna1bp2<em1(IMPC)Tcp>/Ebna1bp2<+>	C57BL/6NCrl-Ebna1bp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414871	F	MP:0001120	abnormal uterus morphology	Ebna1bp2<em1(IMPC)Tcp>/Ebna1bp2<+>	C57BL/6NCrl-Ebna1bp2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414874	M	MP:0002100	abnormal tooth morphology	Eif3k<em1(IMPC)Hmgu>/Eif3k<+>	C57BL/6NCrl-Eif3k<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414874	F	MP:0010506	prolonged RR interval	Eif3k<em1(IMPC)Hmgu>/Eif3k<+>	C57BL/6NCrl-Eif3k<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414874	M	MP:0005568	increased circulating total protein level	Eif3k<em1(IMPC)Hmgu>/Eif3k<+>	C57BL/6NCrl-Eif3k<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414876	M	MP:0001529	abnormal vocalization	Eif4g1<em1(IMPC)Hmgu>/Eif4g1<+>	C57BL/6NCrl-Eif4g1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414876	F	MP:0002941	increased circulating alanine transaminase level	Eif4g1<em1(IMPC)Hmgu>/Eif4g1<+>	C57BL/6NCrl-Eif4g1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414876	M	MP:0013279	increased fasting circulating glucose level	Eif4g1<em1(IMPC)Hmgu>/Eif4g1<+>	C57BL/6NCrl-Eif4g1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414876	M	MP:0011964	increased total retina thickness	Eif4g1<em1(IMPC)Hmgu>/Eif4g1<+>	C57BL/6NCrl-Eif4g1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414876	F	MP:0005343	increased circulating aspartate transaminase level	Eif4g1<em1(IMPC)Hmgu>/Eif4g1<+>	C57BL/6NCrl-Eif4g1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414876	M	MP:0004953	decreased spleen weight	Eif4g1<em1(IMPC)Hmgu>/Eif4g1<+>	C57BL/6NCrl-Eif4g1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414878	F	MP:0000063	decreased bone mineral density	Etv6<em1(IMPC)Rbrc>/Etv6<+>	C57BL/6NJcl-Etv6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414878	F	MP:0005567	decreased circulating total protein level	Etv6<em1(IMPC)Rbrc>/Etv6<+>	C57BL/6NJcl-Etv6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414878	F	MP:0000195	decreased circulating calcium level	Etv6<em1(IMPC)Rbrc>/Etv6<+>	C57BL/6NJcl-Etv6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414878	F	MP:0003917	increased kidney weight	Etv6<em1(IMPC)Rbrc>/Etv6<+>	C57BL/6NJcl-Etv6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414878	F	MP:0004857	abnormal heart weight	Etv6<em1(IMPC)Rbrc>/Etv6<+>	C57BL/6NJcl-Etv6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414878	F	MP:0005179	decreased circulating cholesterol level	Etv6<em1(IMPC)Rbrc>/Etv6<+>	C57BL/6NJcl-Etv6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414878	F	MP:0004952	increased spleen weight	Etv6<em1(IMPC)Rbrc>/Etv6<+>	C57BL/6NJcl-Etv6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414878	F	MP:0008821	increased blood uric acid level	Etv6<em1(IMPC)Rbrc>/Etv6<+>	C57BL/6NJcl-Etv6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414878	F	MP:0000186	decreased circulating HDL cholesterol level	Etv6<em1(IMPC)Rbrc>/Etv6<+>	C57BL/6NJcl-Etv6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414878	M	MP:0000277	abnormal heart shape	Etv6<em1(IMPC)Rbrc>/Etv6<+>	C57BL/6NJcl-Etv6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414878	F	MP:0005419	decreased circulating serum albumin level	Etv6<em1(IMPC)Rbrc>/Etv6<+>	C57BL/6NJcl-Etv6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414880	F	MP:0005560	decreased circulating glucose level	Exoc6b<em1(IMPC)Hmgu>/Exoc6b<+>	C57BL/6NCrl-Exoc6b<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414882	M	MP:0000689	abnormal spleen morphology	Fa2h<em1(IMPC)Mbp>/Fa2h<em1(IMPC)Mbp>	C57BL/6NCrl-Fa2h<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414882	M	MP:0001148	enlarged testis	Fa2h<em1(IMPC)Mbp>/Fa2h<em1(IMPC)Mbp>	C57BL/6NCrl-Fa2h<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414882	M	MP:0010053	decreased grip strength	Fa2h<em1(IMPC)Mbp>/Fa2h<em1(IMPC)Mbp>	C57BL/6NCrl-Fa2h<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414882	F	MP:0002092	abnormal eye morphology	Fa2h<em1(IMPC)Mbp>/Fa2h<em1(IMPC)Mbp>	C57BL/6NCrl-Fa2h<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414882	M	MP:0002135	abnormal kidney morphology	Fa2h<em1(IMPC)Mbp>/Fa2h<em1(IMPC)Mbp>	C57BL/6NCrl-Fa2h<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414882	M	MP:0005179	decreased circulating cholesterol level	Fa2h<em1(IMPC)Mbp>/Fa2h<em1(IMPC)Mbp>	C57BL/6NCrl-Fa2h<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414882	M	MP:0000691	enlarged spleen	Fa2h<em1(IMPC)Mbp>/Fa2h<em1(IMPC)Mbp>	C57BL/6NCrl-Fa2h<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414882	M	MP:0003068	enlarged kidney	Fa2h<em1(IMPC)Mbp>/Fa2h<em1(IMPC)Mbp>	C57BL/6NCrl-Fa2h<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414882	M	MP:0020421	increased freezing behavior	Fa2h<em1(IMPC)Mbp>/Fa2h<em1(IMPC)Mbp>	C57BL/6NCrl-Fa2h<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414882	M	MP:0001146	abnormal testis morphology	Fa2h<em1(IMPC)Mbp>/Fa2h<em1(IMPC)Mbp>	C57BL/6NCrl-Fa2h<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414883	F	MP:0008810	increased circulating iron level	Faah<em1(IMPC)H>/Faah<em1(IMPC)H>	C57BL/6NTac-Faah<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414883	F	MP:0005560	decreased circulating glucose level	Faah<em1(IMPC)H>/Faah<em1(IMPC)H>	C57BL/6NTac-Faah<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414883	F	MP:0002599	increased mean platelet volume	Faah<em1(IMPC)H>/Faah<em1(IMPC)H>	C57BL/6NTac-Faah<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414884	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Fam135a<em1(IMPC)Tcp>/Fam135a<em1(IMPC)Tcp>	C57BL/6NCrl-Fam135a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414884	M	MP:0020421	increased freezing behavior	Fam135a<em1(IMPC)Tcp>/Fam135a<em1(IMPC)Tcp>	C57BL/6NCrl-Fam135a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414884	F	MP:0002792	abnormal retina vasculature morphology	Fam135a<em1(IMPC)Tcp>/Fam135a<em1(IMPC)Tcp>	C57BL/6NCrl-Fam135a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414884	M	MP:0001363	increased anxiety-related response	Fam135a<em1(IMPC)Tcp>/Fam135a<em1(IMPC)Tcp>	C57BL/6NCrl-Fam135a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414884	M	MP:0001402	decreased locomotor activity	Fam135a<em1(IMPC)Tcp>/Fam135a<em1(IMPC)Tcp>	C57BL/6NCrl-Fam135a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414884	F	MP:0010097	abnormal retina blood vessel morphology	Fam135a<em1(IMPC)Tcp>/Fam135a<em1(IMPC)Tcp>	C57BL/6NCrl-Fam135a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414884	F	MP:0001303	abnormal lens morphology	Fam135a<em1(IMPC)Tcp>/Fam135a<em1(IMPC)Tcp>	C57BL/6NCrl-Fam135a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414884	F	MP:0001304	cataract	Fam135a<em1(IMPC)Tcp>/Fam135a<em1(IMPC)Tcp>	C57BL/6NCrl-Fam135a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414884	M	MP:0005562	decreased mean corpuscular hemoglobin	Fam135a<em1(IMPC)Tcp>/Fam135a<em1(IMPC)Tcp>	C57BL/6NCrl-Fam135a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414884	M	MP:0002060	abnormal skin morphology	Fam135a<em1(IMPC)Tcp>/Fam135a<em1(IMPC)Tcp>	C57BL/6NCrl-Fam135a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414886	M	MP:0002339	abnormal lymph node morphology	Spata31f3<em1(IMPC)Ccpcz>/Spata31f3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Spata31f3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414886	M	MP:0008078	increased CD8-positive, alpha-beta T cell number	Spata31f3<em1(IMPC)Ccpcz>/Spata31f3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Spata31f3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414886	M	MP:0001147	small testis	Spata31f3<em1(IMPC)Ccpcz>/Spata31f3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Spata31f3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414886	M	MP:0000702	enlarged lymph nodes	Spata31f3<em1(IMPC)Ccpcz>/Spata31f3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Spata31f3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414886	M	MP:0001146	abnormal testis morphology	Spata31f3<em1(IMPC)Ccpcz>/Spata31f3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Spata31f3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414886	M	MP:0013436	increased CD8-positive, naive alpha-beta T cell number	Spata31f3<em1(IMPC)Ccpcz>/Spata31f3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Spata31f3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414886	M	MP:0000266	abnormal heart morphology	Spata31f3<em1(IMPC)Ccpcz>/Spata31f3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Spata31f3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414886	M	MP:0000274	enlarged heart	Spata31f3<em1(IMPC)Ccpcz>/Spata31f3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Spata31f3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414887	M	MP:0000689	abnormal spleen morphology	Fam83b<em1(IMPC)Mbp>/Fam83b<em1(IMPC)Mbp>	C57BL/6NCrl-Fam83b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414887	M	MP:0001146	abnormal testis morphology	Fam83b<em1(IMPC)Mbp>/Fam83b<em1(IMPC)Mbp>	C57BL/6NCrl-Fam83b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414887	F	MP:0002989	small kidney	Fam83b<em1(IMPC)Mbp>/Fam83b<em1(IMPC)Mbp>	C57BL/6NCrl-Fam83b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414887	M	MP:0000691	enlarged spleen	Fam83b<em1(IMPC)Mbp>/Fam83b<em1(IMPC)Mbp>	C57BL/6NCrl-Fam83b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414887	M	MP:0001304	cataract	Fam83b<em1(IMPC)Mbp>/Fam83b<em1(IMPC)Mbp>	C57BL/6NCrl-Fam83b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414887	F	MP:0002135	abnormal kidney morphology	Fam83b<em1(IMPC)Mbp>/Fam83b<em1(IMPC)Mbp>	C57BL/6NCrl-Fam83b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414887	M	MP:0001148	enlarged testis	Fam83b<em1(IMPC)Mbp>/Fam83b<em1(IMPC)Mbp>	C57BL/6NCrl-Fam83b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414888	M	MP:0010097	abnormal retina blood vessel morphology	Fancd2<em1(IMPC)Hmgu>/Fancd2<+>	C57BL/6NCrl-Fancd2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414888	M	MP:0001289	persistence of hyaloid vascular system	Fancd2<em1(IMPC)Hmgu>/Fancd2<+>	C57BL/6NCrl-Fancd2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414888	F	MP:0002989	small kidney	Fancd2<em1(IMPC)Hmgu>/Fancd2<+>	C57BL/6NCrl-Fancd2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414888	F	MP:0008810	increased circulating iron level	Fancd2<em1(IMPC)Hmgu>/Fancd2<+>	C57BL/6NCrl-Fancd2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414890	M	MP:0005016	decreased lymphocyte cell number	Fbn1<em1(IMPC)H>/Fbn1<+>	C57BL/6NTac-Fbn1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414890	F	MP:0002599	increased mean platelet volume	Fbn1<em1(IMPC)H>/Fbn1<+>	C57BL/6NTac-Fbn1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414890	M	MP:0000219	increased neutrophil cell number	Fbn1<em1(IMPC)H>/Fbn1<+>	C57BL/6NTac-Fbn1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414891	M	MP:0008259	abnormal optic disk morphology	Fbn2<em1(IMPC)Rbrc>/Fbn2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fbn2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414891	F	MP:0004857	abnormal heart weight	Fbn2<em1(IMPC)Rbrc>/Fbn2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fbn2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414891	M	MP:0003179	thrombocytopenia	Fbn2<em1(IMPC)Rbrc>/Fbn2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fbn2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414891	F	MP:0000150	abnormal rib morphology	Fbn2<em1(IMPC)Rbrc>/Fbn2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fbn2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414891	F	MP:0002968	increased circulating alkaline phosphatase level	Fbn2<em1(IMPC)Rbrc>/Fbn2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fbn2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414891	F	MP:0005542	cornea vascularization	Fbn2<em1(IMPC)Rbrc>/Fbn2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fbn2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414891	M	MP:0010123	increased bone mineral content	Fbn2<em1(IMPC)Rbrc>/Fbn2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fbn2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414891	F	MP:0003795	abnormal bone structure	Fbn2<em1(IMPC)Rbrc>/Fbn2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fbn2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414892	F	MP:0000689	abnormal spleen morphology	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	M	MP:0003961	decreased lean body mass	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	M	MP:0000274	enlarged heart	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	M	MP:0002152	abnormal brain morphology	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	M	MP:0003402	decreased liver weight	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	M	MP:0000266	abnormal heart morphology	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	M	MP:0013771	decreased effector memory T-helper cell number	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	F	MP:0000759	abnormal skeletal muscle morphology	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	M	MP:0003271	abnormal duodenum morphology	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	M	MP:0001146	abnormal testis morphology	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	M	MP:0002968	increased circulating alkaline phosphatase level	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	M	MP:0001891	hydrocephaly	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	M	MP:0003019	increased circulating chloride level	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	M	MP:0001148	enlarged testis	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	M	MP:0005567	decreased circulating total protein level	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414892	F	MP:0002060	abnormal skin morphology	Fbxl3<em1(IMPC)Ccpcz>/Fbxl3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxl3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414893	F	MP:0004002	abnormal jejunum morphology	Fdx2<em1(IMPC)Rbrc>/Fdx2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fdx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414893	F	MP:0005563	abnormal hemoglobin content	Fdx2<em1(IMPC)Rbrc>/Fdx2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fdx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414893	F	MP:0003917	increased kidney weight	Fdx2<em1(IMPC)Rbrc>/Fdx2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fdx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414893	F	MP:0000598	abnormal liver morphology	Fdx2<em1(IMPC)Rbrc>/Fdx2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fdx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414893	F	MP:0004952	increased spleen weight	Fdx2<em1(IMPC)Rbrc>/Fdx2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fdx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414893	F	MP:0001586	abnormal erythrocyte cell number	Fdx2<em1(IMPC)Rbrc>/Fdx2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fdx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414893	F	MP:0012360	abnormal large unstained cell number	Fdx2<em1(IMPC)Rbrc>/Fdx2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fdx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414893	F	MP:0004857	abnormal heart weight	Fdx2<em1(IMPC)Rbrc>/Fdx2<em1(IMPC)Rbrc>	C57BL/6NJcl-Fdx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414895	F	MP:0000601	small liver	Ffar3<em1(IMPC)Mbp>/Ffar3<em1(IMPC)Mbp>	C57BL/6NCrl-Ffar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414895	M	MP:0002135	abnormal kidney morphology	Ffar3<em1(IMPC)Mbp>/Ffar3<em1(IMPC)Mbp>	C57BL/6NCrl-Ffar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414895	F	MP:0002092	abnormal eye morphology	Ffar3<em1(IMPC)Mbp>/Ffar3<em1(IMPC)Mbp>	C57BL/6NCrl-Ffar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414895	M	MP:0003068	enlarged kidney	Ffar3<em1(IMPC)Mbp>/Ffar3<em1(IMPC)Mbp>	C57BL/6NCrl-Ffar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414895	F	MP:0000598	abnormal liver morphology	Ffar3<em1(IMPC)Mbp>/Ffar3<em1(IMPC)Mbp>	C57BL/6NCrl-Ffar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414895	F	MP:0001297	microphthalmia	Ffar3<em1(IMPC)Mbp>/Ffar3<em1(IMPC)Mbp>	C57BL/6NCrl-Ffar3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	F	MP:0020870	decreased thigmotaxis	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	M	MP:0001146	abnormal testis morphology	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	F	MP:0010097	abnormal retina blood vessel morphology	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	M	MP:0002060	abnormal skin morphology	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	M	MP:0001289	persistence of hyaloid vascular system	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	M	MP:0002792	abnormal retina vasculature morphology	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	M	MP:0002135	abnormal kidney morphology	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	M	MP:0005179	decreased circulating cholesterol level	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	F	MP:0001364	decreased anxiety-related response	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	F	MP:0000601	small liver	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	F	MP:0004924	abnormal behavior	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	F	MP:0000266	abnormal heart morphology	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	M	MP:0003068	enlarged kidney	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	M	MP:0001147	small testis	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	F	MP:0000274	enlarged heart	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	F	MP:0000598	abnormal liver morphology	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414896	F	MP:0001402	decreased locomotor activity	Fgd5<em1(IMPC)Mbp>/Fgd5<+>	C57BL/6NCrl-Fgd5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414898	F	MP:0009709	hydrometra	Flt3<em1(IMPC)Ccpcz>/Flt3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Flt3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414898	M	MP:0000266	abnormal heart morphology	Flt3<em1(IMPC)Ccpcz>/Flt3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Flt3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414898	F	MP:0000689	abnormal spleen morphology	Flt3<em1(IMPC)Ccpcz>/Flt3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Flt3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414898	M	MP:0003961	decreased lean body mass	Flt3<em1(IMPC)Ccpcz>/Flt3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Flt3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414898	F	MP:0013771	decreased effector memory T-helper cell number	Flt3<em1(IMPC)Ccpcz>/Flt3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Flt3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414898	F	MP:0000759	abnormal skeletal muscle morphology	Flt3<em1(IMPC)Ccpcz>/Flt3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Flt3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414898	M	MP:0000274	enlarged heart	Flt3<em1(IMPC)Ccpcz>/Flt3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Flt3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414898	F	MP:0001120	abnormal uterus morphology	Flt3<em1(IMPC)Ccpcz>/Flt3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Flt3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414898	F	MP:0002092	abnormal eye morphology	Flt3<em1(IMPC)Ccpcz>/Flt3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Flt3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414899	M	MP:0004924	abnormal behavior	Ftl1<em1(IMPC)Rbrc>/Ftl1<em1(IMPC)Rbrc>	C57BL/6NJcl-Ftl1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414900	F	MP:0000266	abnormal heart morphology	Ftl2-ps<em1(IMPC)Rbrc>/Ftl2-ps<em1(IMPC)Rbrc>	C57BL/6NJcl-Ftl2-ps<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414900	F	MP:0000274	enlarged heart	Ftl2-ps<em1(IMPC)Rbrc>/Ftl2-ps<em1(IMPC)Rbrc>	C57BL/6NJcl-Ftl2-ps<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414901	M	MP:0002834	decreased heart weight	Gabrg2<em1(IMPC)Mbp>/Gabrg2<+>	C57BL/6NCrl-Gabrg2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414901	F	MP:0001126	abnormal ovary morphology	Gabrg2<em1(IMPC)Mbp>/Gabrg2<+>	C57BL/6NCrl-Gabrg2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414901	M	MP:0001148	enlarged testis	Gabrg2<em1(IMPC)Mbp>/Gabrg2<+>	C57BL/6NCrl-Gabrg2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414901	M	MP:0000063	decreased bone mineral density	Gabrg2<em1(IMPC)Mbp>/Gabrg2<+>	C57BL/6NCrl-Gabrg2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414901	M	MP:0001146	abnormal testis morphology	Gabrg2<em1(IMPC)Mbp>/Gabrg2<+>	C57BL/6NCrl-Gabrg2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414901	F	MP:0002060	abnormal skin morphology	Gabrg2<em1(IMPC)Mbp>/Gabrg2<+>	C57BL/6NCrl-Gabrg2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414903	F	MP:0005419	decreased circulating serum albumin level	Galr2<em1(IMPC)H>/Galr2<em1(IMPC)H>	C57BL/6NTac-Galr2<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414904	F	MP:0000221	decreased leukocyte cell number	Gdf5<em1(IMPC)H>/Gdf5<em1(IMPC)H>	C57BL/6NTac-Gdf5<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414904	M	MP:0000062	increased bone mineral density	Gdf5<em1(IMPC)H>/Gdf5<em1(IMPC)H>	C57BL/6NTac-Gdf5<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414904	F	MP:0001513	limb grasping	Gdf5<em1(IMPC)H>/Gdf5<em1(IMPC)H>	C57BL/6NTac-Gdf5<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414904	F	MP:0003795	abnormal bone structure	Gdf5<em1(IMPC)H>/Gdf5<em1(IMPC)H>	C57BL/6NTac-Gdf5<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414904	F	MP:0005016	decreased lymphocyte cell number	Gdf5<em1(IMPC)H>/Gdf5<em1(IMPC)H>	C57BL/6NTac-Gdf5<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414905	F	MP:0002574	increased vertical activity	Gm614<em1(IMPC)Bay>/Gm614<+>	C57BL/6N-Gm614<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414906	F	MP:0005553	increased circulating creatinine level	Gpd1<em1(IMPC)Hmgu>/Gpd1<em1(IMPC)Hmgu>	C57BL/6NCrl-Gpd1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414906	F	MP:0001566	increased circulating phosphate level	Gpd1<em1(IMPC)Hmgu>/Gpd1<em1(IMPC)Hmgu>	C57BL/6NCrl-Gpd1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414906	F	MP:0005627	increased circulating potassium level	Gpd1<em1(IMPC)Hmgu>/Gpd1<em1(IMPC)Hmgu>	C57BL/6NCrl-Gpd1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414906	M	MP:0001406	abnormal gait	Gpd1<em1(IMPC)Hmgu>/Gpd1<em1(IMPC)Hmgu>	C57BL/6NCrl-Gpd1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414909	F	MP:0006352	decreased glycosylated hemoglobin level	Gypc<em1(IMPC)Rbrc>/Gypc<em1(IMPC)Rbrc>	C57BL/6NJcl-Gypc<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414910	M	MP:0001304	cataract	Gzf1<em1(IMPC)Tcp>/Gzf1<+>	C57BL/6NCrl-Gzf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414910	M	MP:0001303	abnormal lens morphology	Gzf1<em1(IMPC)Tcp>/Gzf1<+>	C57BL/6NCrl-Gzf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414910	F	MP:0002966	decreased circulating alkaline phosphatase level	Gzf1<em1(IMPC)Tcp>/Gzf1<+>	C57BL/6NCrl-Gzf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414911	F	MP:0003795	abnormal bone structure	Gzf1<em1(IMPC)Tcp>/Gzf1<em1(IMPC)Tcp>	C57BL/6NCrl-Gzf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414911	M	MP:0002060	abnormal skin morphology	Gzf1<em1(IMPC)Tcp>/Gzf1<em1(IMPC)Tcp>	C57BL/6NCrl-Gzf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414911	F	MP:0010024	increased total body fat amount	Gzf1<em1(IMPC)Tcp>/Gzf1<em1(IMPC)Tcp>	C57BL/6NCrl-Gzf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414911	F	MP:0002764	short tibia	Gzf1<em1(IMPC)Tcp>/Gzf1<em1(IMPC)Tcp>	C57BL/6NCrl-Gzf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414911	F	MP:0002966	decreased circulating alkaline phosphatase level	Gzf1<em1(IMPC)Tcp>/Gzf1<em1(IMPC)Tcp>	C57BL/6NCrl-Gzf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414911	F	MP:0003961	decreased lean body mass	Gzf1<em1(IMPC)Tcp>/Gzf1<em1(IMPC)Tcp>	C57BL/6NCrl-Gzf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414911	F	MP:0002092	abnormal eye morphology	Gzf1<em1(IMPC)Tcp>/Gzf1<em1(IMPC)Tcp>	C57BL/6NCrl-Gzf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414911	F	MP:0005567	decreased circulating total protein level	Gzf1<em1(IMPC)Tcp>/Gzf1<em1(IMPC)Tcp>	C57BL/6NCrl-Gzf1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414913	M	MP:0000157	abnormal sternum morphology	Hagh<em1(IMPC)Tcp>/Hagh<em1(IMPC)Tcp>	C57BL/6NCrl-Hagh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414913	F	MP:0001303	abnormal lens morphology	Hagh<em1(IMPC)Tcp>/Hagh<em1(IMPC)Tcp>	C57BL/6NCrl-Hagh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414913	M	MP:0010067	increased red blood cell distribution width	Hagh<em1(IMPC)Tcp>/Hagh<em1(IMPC)Tcp>	C57BL/6NCrl-Hagh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414913	M	MP:0000208	decreased hematocrit	Hagh<em1(IMPC)Tcp>/Hagh<em1(IMPC)Tcp>	C57BL/6NCrl-Hagh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414913	M	MP:0002591	decreased mean corpuscular volume	Hagh<em1(IMPC)Tcp>/Hagh<em1(IMPC)Tcp>	C57BL/6NCrl-Hagh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414913	F	MP:0001304	cataract	Hagh<em1(IMPC)Tcp>/Hagh<em1(IMPC)Tcp>	C57BL/6NCrl-Hagh<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414914	F	MP:0000598	abnormal liver morphology	Hikeshi<em1(IMPC)Rbrc>/Hikeshi<+>	C57BL/6NJcl-Hikeshi<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414916	F	MP:0001257	increased body length	Hltf<em1(IMPC)Bay>/Hltf<+>	C57BL/6N-Hltf<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414919	M	MP:0008805	decreased circulating amylase level	Hr<em1(IMPC)H>/Hr<em1(IMPC)H>	C57BL/6NTac-Hr<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414919	F	MP:0002966	decreased circulating alkaline phosphatase level	Hr<em1(IMPC)H>/Hr<em1(IMPC)H>	C57BL/6NTac-Hr<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414920	M	MP:0002135	abnormal kidney morphology	Hrh1<em1(IMPC)Rbrc>/Hrh1<em1(IMPC)Rbrc>	C57BL/6NJcl-Hrh1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414922	F	MP:0010052	increased grip strength	Htt<em1(IMPC)H>/Htt<+>	C57BL/6NTac-Htt<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414924	F	MP:0002135	abnormal kidney morphology	Ikzf4<em1(IMPC)Rbrc>/Ikzf4<em1(IMPC)Rbrc>	C57BL/6NJcl-Ikzf4<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414924	F	MP:0001402	decreased locomotor activity	Ikzf4<em1(IMPC)Rbrc>/Ikzf4<em1(IMPC)Rbrc>	C57BL/6NJcl-Ikzf4<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414925	F	MP:0001120	abnormal uterus morphology	Il17ra<em1(IMPC)Mbp>/Il17ra<em1(IMPC)Mbp>	C57BL/6NCrl-Il17ra<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414925	F	MP:0001126	abnormal ovary morphology	Il17ra<em1(IMPC)Mbp>/Il17ra<em1(IMPC)Mbp>	C57BL/6NCrl-Il17ra<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414925	F	MP:0000598	abnormal liver morphology	Il17ra<em1(IMPC)Mbp>/Il17ra<em1(IMPC)Mbp>	C57BL/6NCrl-Il17ra<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414925	F	MP:0000601	small liver	Il17ra<em1(IMPC)Mbp>/Il17ra<em1(IMPC)Mbp>	C57BL/6NCrl-Il17ra<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414926	M	MP:0002092	abnormal eye morphology	Il25<em1(IMPC)Mbp>/Il25<em1(IMPC)Mbp>	C57BL/6NCrl-Il25<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414926	M	MP:0001297	microphthalmia	Il25<em1(IMPC)Mbp>/Il25<em1(IMPC)Mbp>	C57BL/6NCrl-Il25<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414926	M	MP:0001146	abnormal testis morphology	Il25<em1(IMPC)Mbp>/Il25<em1(IMPC)Mbp>	C57BL/6NCrl-Il25<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414926	M	MP:0001148	enlarged testis	Il25<em1(IMPC)Mbp>/Il25<em1(IMPC)Mbp>	C57BL/6NCrl-Il25<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414926	M	MP:0010392	prolonged QRS complex duration	Il25<em1(IMPC)Mbp>/Il25<em1(IMPC)Mbp>	C57BL/6NCrl-Il25<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414926	M	MP:0001304	cataract	Il25<em1(IMPC)Mbp>/Il25<em1(IMPC)Mbp>	C57BL/6NCrl-Il25<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414926	M	MP:0001147	small testis	Il25<em1(IMPC)Mbp>/Il25<em1(IMPC)Mbp>	C57BL/6NCrl-Il25<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414927	F	MP:0000601	small liver	Il9<em1(IMPC)Mbp>/Il9<em1(IMPC)Mbp>	C57BL/6NCrl-Il9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414927	F	MP:0002989	small kidney	Il9<em1(IMPC)Mbp>/Il9<em1(IMPC)Mbp>	C57BL/6NCrl-Il9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414927	F	MP:0002135	abnormal kidney morphology	Il9<em1(IMPC)Mbp>/Il9<em1(IMPC)Mbp>	C57BL/6NCrl-Il9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414927	M	MP:0001148	enlarged testis	Il9<em1(IMPC)Mbp>/Il9<em1(IMPC)Mbp>	C57BL/6NCrl-Il9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414927	M	MP:0001146	abnormal testis morphology	Il9<em1(IMPC)Mbp>/Il9<em1(IMPC)Mbp>	C57BL/6NCrl-Il9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414927	M	MP:0002941	increased circulating alanine transaminase level	Il9<em1(IMPC)Mbp>/Il9<em1(IMPC)Mbp>	C57BL/6NCrl-Il9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414927	F	MP:0001120	abnormal uterus morphology	Il9<em1(IMPC)Mbp>/Il9<em1(IMPC)Mbp>	C57BL/6NCrl-Il9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414927	F	MP:0000689	abnormal spleen morphology	Il9<em1(IMPC)Mbp>/Il9<em1(IMPC)Mbp>	C57BL/6NCrl-Il9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414927	F	MP:0000691	enlarged spleen	Il9<em1(IMPC)Mbp>/Il9<em1(IMPC)Mbp>	C57BL/6NCrl-Il9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414927	F	MP:0000598	abnormal liver morphology	Il9<em1(IMPC)Mbp>/Il9<em1(IMPC)Mbp>	C57BL/6NCrl-Il9<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414928	M	MP:0020870	decreased thigmotaxis	Ilkap<em1(IMPC)Tcp>/Ilkap<em1(IMPC)Tcp>	C57BL/6NCrl-Ilkap<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414933	M	MP:0001914	hemorrhage	Invs<em1(IMPC)Bay>/Invs<em1(IMPC)Bay>	C57BL/6N-Invs<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414933	F	MP:0001785	edema	Invs<em1(IMPC)Bay>/Invs<em1(IMPC)Bay>	C57BL/6N-Invs<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414936	F	MP:0005343	increased circulating aspartate transaminase level	Itgal<em1(IMPC)H>/Itgal<em1(IMPC)H>	C57BL/6NTac-Itgal<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414936	F	MP:0002941	increased circulating alanine transaminase level	Itgal<em1(IMPC)H>/Itgal<em1(IMPC)H>	C57BL/6NTac-Itgal<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414937	M	MP:0010090	increased circulating creatine kinase level	Itgb6<em1(IMPC)Ccpcz>/Itgb6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Itgb6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414937	M	MP:0001262	decreased body weight	Itgb6<em1(IMPC)Ccpcz>/Itgb6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Itgb6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414937	F	MP:0001293	anophthalmia	Itgb6<em1(IMPC)Ccpcz>/Itgb6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Itgb6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414937	M	MP:0010379	decreased respiratory quotient	Itgb6<em1(IMPC)Ccpcz>/Itgb6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Itgb6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414937	M	MP:0013129	abnormal tooth color	Itgb6<em1(IMPC)Ccpcz>/Itgb6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Itgb6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414937	M	MP:0020421	increased freezing behavior	Itgb6<em1(IMPC)Ccpcz>/Itgb6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Itgb6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414937	M	MP:0011048	decreased lung tissue damping	Itgb6<em1(IMPC)Ccpcz>/Itgb6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Itgb6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414937	M	MP:0002060	abnormal skin morphology	Itgb6<em1(IMPC)Ccpcz>/Itgb6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Itgb6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414937	M	MP:0010895	increased lung compliance	Itgb6<em1(IMPC)Ccpcz>/Itgb6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Itgb6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414937	F	MP:0002092	abnormal eye morphology	Itgb6<em1(IMPC)Ccpcz>/Itgb6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Itgb6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414937	M	MP:0011045	decreased lung elastance	Itgb6<em1(IMPC)Ccpcz>/Itgb6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Itgb6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414937	M	MP:0002941	increased circulating alanine transaminase level	Itgb6<em1(IMPC)Ccpcz>/Itgb6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Itgb6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414938	M	MP:0004931	enlarged epididymis	Katna1<em1(IMPC)Rbrc>/Katna1<+>	C57BL/6NJcl-Katna1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414938	M	MP:0002631	abnormal epididymis morphology	Katna1<em1(IMPC)Rbrc>/Katna1<+>	C57BL/6NJcl-Katna1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414938	M	MP:0001148	enlarged testis	Katna1<em1(IMPC)Rbrc>/Katna1<+>	C57BL/6NJcl-Katna1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414940	F	MP:0011874	enlarged urinary bladder	Katnal1<em1(IMPC)Tcp>/Katnal1<+>	C57BL/6NCrl-Katnal1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414940	M	MP:0000702	enlarged lymph nodes	Katnal1<em1(IMPC)Tcp>/Katnal1<+>	C57BL/6NCrl-Katnal1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414940	M	MP:0001303	abnormal lens morphology	Katnal1<em1(IMPC)Tcp>/Katnal1<+>	C57BL/6NCrl-Katnal1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414940	F	MP:0003068	enlarged kidney	Katnal1<em1(IMPC)Tcp>/Katnal1<+>	C57BL/6NCrl-Katnal1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414940	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Katnal1<em1(IMPC)Tcp>/Katnal1<+>	C57BL/6NCrl-Katnal1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414940	M	MP:0002591	decreased mean corpuscular volume	Katnal1<em1(IMPC)Tcp>/Katnal1<+>	C57BL/6NCrl-Katnal1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414941	M	MP:0002060	abnormal skin morphology	Katnal1<em1(IMPC)Tcp>/Katnal1<em1(IMPC)Tcp>	C57BL/6NCrl-Katnal1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414941	M	MP:0000689	abnormal spleen morphology	Katnal1<em1(IMPC)Tcp>/Katnal1<em1(IMPC)Tcp>	C57BL/6NCrl-Katnal1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414941	F	MP:0011100	preweaning lethality, complete penetrance	Katnal1<em1(IMPC)Tcp>/Katnal1<em1(IMPC)Tcp>	C57BL/6NCrl-Katnal1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414942	M	MP:0010067	increased red blood cell distribution width	Kcna2<em1(IMPC)H>/Kcna2<+>	C57BL/6NTac-Kcna2<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414943	M	MP:0001364	decreased anxiety-related response	Kcnc1<em4(IMPC)H>/Kcnc1<em4(IMPC)H>	C57BL/6NTac-Kcnc1<em4(IMPC)H>/H	N	MGI:5576271
MGI:7414943	M	MP:0001415	increased exploration in new environment	Kcnc1<em4(IMPC)H>/Kcnc1<em4(IMPC)H>	C57BL/6NTac-Kcnc1<em4(IMPC)H>/H	N	MGI:5576271
MGI:7414943	M	MP:0005561	increased mean corpuscular hemoglobin	Kcnc1<em4(IMPC)H>/Kcnc1<em4(IMPC)H>	C57BL/6NTac-Kcnc1<em4(IMPC)H>/H	N	MGI:5576271
MGI:7414943	F	MP:0002590	increased mean corpuscular volume	Kcnc1<em4(IMPC)H>/Kcnc1<em4(IMPC)H>	C57BL/6NTac-Kcnc1<em4(IMPC)H>/H	N	MGI:5576271
MGI:7414944	M	MP:0003179	thrombocytopenia	Kctd2<em1(IMPC)Hmgu>/Kctd2<em1(IMPC)Hmgu>	C57BL/6NCrl-Kctd2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414945	F	MP:0000759	abnormal skeletal muscle morphology	Kif16b<em1(IMPC)Ccpcz>/Kif16b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif16b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414945	M	MP:0002059	abnormal seminal vesicle morphology	Kif16b<em1(IMPC)Ccpcz>/Kif16b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif16b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414945	M	MP:0003271	abnormal duodenum morphology	Kif16b<em1(IMPC)Ccpcz>/Kif16b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif16b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414945	F	MP:0000703	abnormal thymus morphology	Kif16b<em1(IMPC)Ccpcz>/Kif16b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif16b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414945	F	MP:0000691	enlarged spleen	Kif16b<em1(IMPC)Ccpcz>/Kif16b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif16b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414945	M	MP:0000495	abnormal colon morphology	Kif16b<em1(IMPC)Ccpcz>/Kif16b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif16b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414945	F	MP:0000709	enlarged thymus	Kif16b<em1(IMPC)Ccpcz>/Kif16b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif16b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414945	M	MP:0002092	abnormal eye morphology	Kif16b<em1(IMPC)Ccpcz>/Kif16b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif16b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414945	M	MP:0001157	small seminal vesicle	Kif16b<em1(IMPC)Ccpcz>/Kif16b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif16b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414945	F	MP:0002060	abnormal skin morphology	Kif16b<em1(IMPC)Ccpcz>/Kif16b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif16b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414946	F	MP:0001297	microphthalmia	Kirrel1<em1(IMPC)Mbp>/Kirrel1<+>	C57BL/6NCrl-Kirrel1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414946	M	MP:0010097	abnormal retina blood vessel morphology	Kirrel1<em1(IMPC)Mbp>/Kirrel1<+>	C57BL/6NCrl-Kirrel1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414947	F	MP:0001297	microphthalmia	Kirrel1<em1(IMPC)Mbp>/Kirrel1<em1(IMPC)Mbp>	C57BL/6NCrl-Kirrel1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414947	F	MP:0003984	embryonic growth retardation	Kirrel1<em1(IMPC)Mbp>/Kirrel1<em1(IMPC)Mbp>	C57BL/6NCrl-Kirrel1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414948	M	MP:0000689	abnormal spleen morphology	Krtap7-1<em1(IMPC)Ccpcz>/Krtap7-1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krtap7-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414948	F	MP:0001312	abnormal cornea morphology	Krtap7-1<em1(IMPC)Ccpcz>/Krtap7-1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krtap7-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414948	F	MP:0000703	abnormal thymus morphology	Krtap7-1<em1(IMPC)Ccpcz>/Krtap7-1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krtap7-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414948	M	MP:0000274	enlarged heart	Krtap7-1<em1(IMPC)Ccpcz>/Krtap7-1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krtap7-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414948	M	MP:0000692	small spleen	Krtap7-1<em1(IMPC)Ccpcz>/Krtap7-1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krtap7-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414948	M	MP:0000266	abnormal heart morphology	Krtap7-1<em1(IMPC)Ccpcz>/Krtap7-1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krtap7-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414948	F	MP:0000709	enlarged thymus	Krtap7-1<em1(IMPC)Ccpcz>/Krtap7-1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krtap7-1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414949	M	MP:0010506	prolonged RR interval	Lamtor3<em1(IMPC)Hmgu>/Lamtor3<+>	C57BL/6NCrl-Lamtor3<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414949	M	MP:0005333	decreased heart rate	Lamtor3<em1(IMPC)Hmgu>/Lamtor3<+>	C57BL/6NCrl-Lamtor3<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414951	F	MP:0001565	abnormal circulating phosphate level	Lcmt1<em1(IMPC)Rbrc>/Lcmt1<+>	C57BL/6NJcl-Lcmt1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414951	F	MP:0004952	increased spleen weight	Lcmt1<em1(IMPC)Rbrc>/Lcmt1<+>	C57BL/6NJcl-Lcmt1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414951	F	MP:0012360	abnormal large unstained cell number	Lcmt1<em1(IMPC)Rbrc>/Lcmt1<+>	C57BL/6NJcl-Lcmt1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414951	F	MP:0000266	abnormal heart morphology	Lcmt1<em1(IMPC)Rbrc>/Lcmt1<+>	C57BL/6NJcl-Lcmt1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414954	F	MP:0001566	increased circulating phosphate level	Lpp<tm1b(KOMP)Wtsi>/Lpp<+>	C57BL/6NCrl-Lpp<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:7414955	F	MP:0001289	persistence of hyaloid vascular system	Lpp<tm1b(KOMP)Wtsi>/Lpp<tm1b(KOMP)Wtsi>	C57BL/6NCrl-Lpp<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:7414955	F	MP:0010097	abnormal retina blood vessel morphology	Lpp<tm1b(KOMP)Wtsi>/Lpp<tm1b(KOMP)Wtsi>	C57BL/6NCrl-Lpp<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:7414955	F	MP:0008259	abnormal optic disk morphology	Lpp<tm1b(KOMP)Wtsi>/Lpp<tm1b(KOMP)Wtsi>	C57BL/6NCrl-Lpp<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:7414955	F	MP:0001325	abnormal retina morphology	Lpp<tm1b(KOMP)Wtsi>/Lpp<tm1b(KOMP)Wtsi>	C57BL/6NCrl-Lpp<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:7414955	F	MP:0002792	abnormal retina vasculature morphology	Lpp<tm1b(KOMP)Wtsi>/Lpp<tm1b(KOMP)Wtsi>	C57BL/6NCrl-Lpp<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:7414956	M	MP:0000274	enlarged heart	Lrrc30<em1(IMPC)Rbrc>/Lrrc30<em1(IMPC)Rbrc>	C57BL/6NJcl-Lrrc30<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414956	M	MP:0000266	abnormal heart morphology	Lrrc30<em1(IMPC)Rbrc>/Lrrc30<em1(IMPC)Rbrc>	C57BL/6NJcl-Lrrc30<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414957	M	MP:0005567	decreased circulating total protein level	Magel2<em2(IMPC)H>/Magel2<em2(IMPC)H>	C57BL/6NTac-Magel2<em2(IMPC)H>/H	N	MGI:5576271
MGI:7414957	F	MP:0001392	abnormal locomotor behavior	Magel2<em2(IMPC)H>/Magel2<em2(IMPC)H>	C57BL/6NTac-Magel2<em2(IMPC)H>/H	N	MGI:5576271
MGI:7414957	M	MP:0005419	decreased circulating serum albumin level	Magel2<em2(IMPC)H>/Magel2<em2(IMPC)H>	C57BL/6NTac-Magel2<em2(IMPC)H>/H	N	MGI:5576271
MGI:7414958	M	MP:0002599	increased mean platelet volume	Magix<em1(IMPC)Hmgu>/Y	C57BL/6NCrl-Magix<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414958	M	MP:0002874	decreased hemoglobin content	Magix<em1(IMPC)Hmgu>/Y	C57BL/6NCrl-Magix<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414958	M	MP:0002875	decreased erythrocyte cell number	Magix<em1(IMPC)Hmgu>/Y	C57BL/6NCrl-Magix<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414958	M	MP:0000221	decreased leukocyte cell number	Magix<em1(IMPC)Hmgu>/Y	C57BL/6NCrl-Magix<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414959	F	MP:0002875	decreased erythrocyte cell number	Magix<em1(IMPC)Hmgu>/Magix<em1(IMPC)Hmgu>	C57BL/6NCrl-Magix<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414959	F	MP:0005553	increased circulating creatinine level	Magix<em1(IMPC)Hmgu>/Magix<em1(IMPC)Hmgu>	C57BL/6NCrl-Magix<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414959	F	MP:0002599	increased mean platelet volume	Magix<em1(IMPC)Hmgu>/Magix<em1(IMPC)Hmgu>	C57BL/6NCrl-Magix<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414960	F	MP:0002699	abnormal vitreous body morphology	Mc5r<em1(IMPC)Mbp>/Mc5r<em1(IMPC)Mbp>	C57BL/6NCrl-Mc5r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414960	F	MP:0000689	abnormal spleen morphology	Mc5r<em1(IMPC)Mbp>/Mc5r<em1(IMPC)Mbp>	C57BL/6NCrl-Mc5r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414960	M	MP:0001148	enlarged testis	Mc5r<em1(IMPC)Mbp>/Mc5r<em1(IMPC)Mbp>	C57BL/6NCrl-Mc5r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414960	M	MP:0005238	increased brain size	Mc5r<em1(IMPC)Mbp>/Mc5r<em1(IMPC)Mbp>	C57BL/6NCrl-Mc5r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414960	F	MP:0000691	enlarged spleen	Mc5r<em1(IMPC)Mbp>/Mc5r<em1(IMPC)Mbp>	C57BL/6NCrl-Mc5r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414960	M	MP:0002152	abnormal brain morphology	Mc5r<em1(IMPC)Mbp>/Mc5r<em1(IMPC)Mbp>	C57BL/6NCrl-Mc5r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414960	M	MP:0001146	abnormal testis morphology	Mc5r<em1(IMPC)Mbp>/Mc5r<em1(IMPC)Mbp>	C57BL/6NCrl-Mc5r<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414962	M	MP:0001614	abnormal blood vessel morphology	Med13l<em1(IMPC)Mbp>/Med13l<em1(IMPC)Mbp>	C57BL/6NCrl-Med13l<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414963	M	MP:0001147	small testis	Mei4<em1(IMPC)Mbp>/Mei4<em1(IMPC)Mbp>	C57BL/6NCrl-Mei4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414963	F	MP:0002989	small kidney	Mei4<em1(IMPC)Mbp>/Mei4<em1(IMPC)Mbp>	C57BL/6NCrl-Mei4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414963	F	MP:0000689	abnormal spleen morphology	Mei4<em1(IMPC)Mbp>/Mei4<em1(IMPC)Mbp>	C57BL/6NCrl-Mei4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414963	F	MP:0002135	abnormal kidney morphology	Mei4<em1(IMPC)Mbp>/Mei4<em1(IMPC)Mbp>	C57BL/6NCrl-Mei4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414963	F	MP:0000691	enlarged spleen	Mei4<em1(IMPC)Mbp>/Mei4<em1(IMPC)Mbp>	C57BL/6NCrl-Mei4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414963	F	MP:0002699	abnormal vitreous body morphology	Mei4<em1(IMPC)Mbp>/Mei4<em1(IMPC)Mbp>	C57BL/6NCrl-Mei4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414963	M	MP:0001146	abnormal testis morphology	Mei4<em1(IMPC)Mbp>/Mei4<em1(IMPC)Mbp>	C57BL/6NCrl-Mei4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414963	F	MP:0005343	increased circulating aspartate transaminase level	Mei4<em1(IMPC)Mbp>/Mei4<em1(IMPC)Mbp>	C57BL/6NCrl-Mei4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414963	F	MP:0002941	increased circulating alanine transaminase level	Mei4<em1(IMPC)Mbp>/Mei4<em1(IMPC)Mbp>	C57BL/6NCrl-Mei4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414966	F	MP:0002135	abnormal kidney morphology	Mid1<em1(IMPC)Mbp>/Mid1<+>	C57BL/6NCrl-Mid1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414966	F	MP:0002833	increased heart weight	Mid1<em1(IMPC)Mbp>/Mid1<+>	C57BL/6NCrl-Mid1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414966	F	MP:0002989	small kidney	Mid1<em1(IMPC)Mbp>/Mid1<+>	C57BL/6NCrl-Mid1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414966	F	MP:0003960	increased lean body mass	Mid1<em1(IMPC)Mbp>/Mid1<+>	C57BL/6NCrl-Mid1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414966	F	MP:0020421	increased freezing behavior	Mid1<em1(IMPC)Mbp>/Mid1<+>	C57BL/6NCrl-Mid1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414966	F	MP:0009142	decreased prepulse inhibition	Mid1<em1(IMPC)Mbp>/Mid1<+>	C57BL/6NCrl-Mid1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414966	F	MP:0010025	decreased total body fat amount	Mid1<em1(IMPC)Mbp>/Mid1<+>	C57BL/6NCrl-Mid1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414967	F	MP:0000691	enlarged spleen	Mid1<em1(IMPC)Mbp>/Mid1<em1(IMPC)Mbp>	C57BL/6NCrl-Mid1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414967	F	MP:0000689	abnormal spleen morphology	Mid1<em1(IMPC)Mbp>/Mid1<em1(IMPC)Mbp>	C57BL/6NCrl-Mid1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414968	F	MP:0011100	preweaning lethality, complete penetrance	Midn<em1(IMPC)Bay>/Midn<em1(IMPC)Bay>	C57BL/6N-Midn<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414969	F	MP:0010506	prolonged RR interval	Mmab<em1(IMPC)Hmgu>/Mmab<+>	C57BL/6NCrl-Mmab<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414969	M	MP:0000689	abnormal spleen morphology	Mmab<em1(IMPC)Hmgu>/Mmab<+>	C57BL/6NCrl-Mmab<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414971	F	MP:0009141	increased prepulse inhibition	Mmp20<em1(IMPC)Ccpcz>/Mmp20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414971	M	MP:0010379	decreased respiratory quotient	Mmp20<em1(IMPC)Ccpcz>/Mmp20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414971	M	MP:0001157	small seminal vesicle	Mmp20<em1(IMPC)Ccpcz>/Mmp20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414971	F	MP:0000689	abnormal spleen morphology	Mmp20<em1(IMPC)Ccpcz>/Mmp20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414971	M	MP:0003961	decreased lean body mass	Mmp20<em1(IMPC)Ccpcz>/Mmp20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414971	M	MP:0002059	abnormal seminal vesicle morphology	Mmp20<em1(IMPC)Ccpcz>/Mmp20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414971	F	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	Mmp20<em1(IMPC)Ccpcz>/Mmp20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414974	F	MP:0001257	increased body length	Mob1a<em1(IMPC)Bay>/Mob1a<+>	C57BL/6N-Mob1a<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414974	M	MP:0003233	prolonged QT interval	Mob1a<em1(IMPC)Bay>/Mob1a<+>	C57BL/6N-Mob1a<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414976	F	MP:0011965	decreased total retina thickness	Mogat1<em1(IMPC)Hmgu>/Mogat1<em1(IMPC)Hmgu>	C57BL/6NCrl-Mogat1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414978	F	MP:0001417	decreased exploration in new environment	Mras<em1(IMPC)H>/Mras<em1(IMPC)H>	C57BL/6NTac-Mras<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414978	M	MP:0005553	increased circulating creatinine level	Mras<em1(IMPC)H>/Mras<em1(IMPC)H>	C57BL/6NTac-Mras<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414978	M	MP:0010025	decreased total body fat amount	Mras<em1(IMPC)H>/Mras<em1(IMPC)H>	C57BL/6NTac-Mras<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414978	M	MP:0003960	increased lean body mass	Mras<em1(IMPC)H>/Mras<em1(IMPC)H>	C57BL/6NTac-Mras<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414979	F	MP:0005553	increased circulating creatinine level	Mtarc1<em1(IMPC)H>/Mtarc1<em1(IMPC)H>	C57BL/6NTac-Mtarc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414979	F	MP:0001566	increased circulating phosphate level	Mtarc1<em1(IMPC)H>/Mtarc1<em1(IMPC)H>	C57BL/6NTac-Mtarc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414979	M	MP:0004952	increased spleen weight	Mtarc1<em1(IMPC)H>/Mtarc1<em1(IMPC)H>	C57BL/6NTac-Mtarc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414979	F	MP:0005565	increased blood urea nitrogen level	Mtarc1<em1(IMPC)H>/Mtarc1<em1(IMPC)H>	C57BL/6NTac-Mtarc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414980	M	MP:0001200	thick skin	Mtmr11<em1(IMPC)Tcp>/Mtmr11<em1(IMPC)Tcp>	C57BL/6NCrl-Mtmr11<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414980	M	MP:0000702	enlarged lymph nodes	Mtmr11<em1(IMPC)Tcp>/Mtmr11<em1(IMPC)Tcp>	C57BL/6NCrl-Mtmr11<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414980	M	MP:0002059	abnormal seminal vesicle morphology	Mtmr11<em1(IMPC)Tcp>/Mtmr11<em1(IMPC)Tcp>	C57BL/6NCrl-Mtmr11<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414980	M	MP:0000691	enlarged spleen	Mtmr11<em1(IMPC)Tcp>/Mtmr11<em1(IMPC)Tcp>	C57BL/6NCrl-Mtmr11<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414980	M	MP:0000157	abnormal sternum morphology	Mtmr11<em1(IMPC)Tcp>/Mtmr11<em1(IMPC)Tcp>	C57BL/6NCrl-Mtmr11<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414981	F	MP:0002966	decreased circulating alkaline phosphatase level	Mtmr2<em1(IMPC)Hmgu>/Mtmr2<em1(IMPC)Hmgu>	C57BL/6NCrl-Mtmr2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414981	M	MP:0001489	decreased startle reflex	Mtmr2<em1(IMPC)Hmgu>/Mtmr2<em1(IMPC)Hmgu>	C57BL/6NCrl-Mtmr2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7414982	M	MP:0010123	increased bone mineral content	Myh2<em1(IMPC)Bay>/Myh2<em1(IMPC)Bay>	C57BL/6N-Myh2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7414984	M	MP:0001399	hyperactivity	Nlgn3<em1(IMPC)Rbrc>/Y	C57BL/6NJcl-Nlgn3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414984	M	MP:0002602	abnormal eosinophil cell number	Nlgn3<em1(IMPC)Rbrc>/Y	C57BL/6NJcl-Nlgn3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414984	M	MP:0010066	abnormal red blood cell distribution width	Nlgn3<em1(IMPC)Rbrc>/Y	C57BL/6NJcl-Nlgn3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414984	M	MP:0008820	abnormal blood uric acid level	Nlgn3<em1(IMPC)Rbrc>/Y	C57BL/6NJcl-Nlgn3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414984	M	MP:0005563	abnormal hemoglobin content	Nlgn3<em1(IMPC)Rbrc>/Y	C57BL/6NJcl-Nlgn3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414984	M	MP:0002596	abnormal hematocrit	Nlgn3<em1(IMPC)Rbrc>/Y	C57BL/6NJcl-Nlgn3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414984	M	MP:0003313	abnormal locomotor activation	Nlgn3<em1(IMPC)Rbrc>/Y	C57BL/6NJcl-Nlgn3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414984	M	MP:0000062	increased bone mineral density	Nlgn3<em1(IMPC)Rbrc>/Y	C57BL/6NJcl-Nlgn3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414985	F	MP:0012440	abnormal neutrophil cell number	Nlgn3<em1(IMPC)Rbrc>/Nlgn3<em1(IMPC)Rbrc>	C57BL/6NJcl-Nlgn3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414985	F	MP:0001399	hyperactivity	Nlgn3<em1(IMPC)Rbrc>/Nlgn3<em1(IMPC)Rbrc>	C57BL/6NJcl-Nlgn3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414985	F	MP:0001364	decreased anxiety-related response	Nlgn3<em1(IMPC)Rbrc>/Nlgn3<em1(IMPC)Rbrc>	C57BL/6NJcl-Nlgn3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414986	F	MP:0010024	increased total body fat amount	Npy5r<em1(IMPC)H>/Npy5r<em1(IMPC)H>	C57BL/6NTac-Npy5r<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414986	F	MP:0003961	decreased lean body mass	Npy5r<em1(IMPC)H>/Npy5r<em1(IMPC)H>	C57BL/6NTac-Npy5r<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414986	F	MP:0001556	increased circulating HDL cholesterol level	Npy5r<em1(IMPC)H>/Npy5r<em1(IMPC)H>	C57BL/6NTac-Npy5r<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414986	F	MP:0002968	increased circulating alkaline phosphatase level	Npy5r<em1(IMPC)H>/Npy5r<em1(IMPC)H>	C57BL/6NTac-Npy5r<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414986	F	MP:0001402	decreased locomotor activity	Npy5r<em1(IMPC)H>/Npy5r<em1(IMPC)H>	C57BL/6NTac-Npy5r<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414987	M	MP:0002965	increased circulating serum albumin level	Nrgn<em1(IMPC)H>/Nrgn<em1(IMPC)H>	C57BL/6NTac-Nrgn<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414987	M	MP:0001392	abnormal locomotor behavior	Nrgn<em1(IMPC)H>/Nrgn<em1(IMPC)H>	C57BL/6NTac-Nrgn<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414987	M	MP:0008805	decreased circulating amylase level	Nrgn<em1(IMPC)H>/Nrgn<em1(IMPC)H>	C57BL/6NTac-Nrgn<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414988	F	MP:0000208	decreased hematocrit	Nsun5<tm2b(EUCOMM)Wtsi>/Nsun5<tm2b(EUCOMM)Wtsi>	C57BL/6NJ-Nsun5<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:7414988	F	MP:0002875	decreased erythrocyte cell number	Nsun5<tm2b(EUCOMM)Wtsi>/Nsun5<tm2b(EUCOMM)Wtsi>	C57BL/6NJ-Nsun5<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:7414988	M	MP:0002941	increased circulating alanine transaminase level	Nsun5<tm2b(EUCOMM)Wtsi>/Nsun5<tm2b(EUCOMM)Wtsi>	C57BL/6NJ-Nsun5<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:7414988	F	MP:0002874	decreased hemoglobin content	Nsun5<tm2b(EUCOMM)Wtsi>/Nsun5<tm2b(EUCOMM)Wtsi>	C57BL/6NJ-Nsun5<tm2b(EUCOMM)Wtsi>/J	N	MGI:5576271
MGI:7414989	M	MP:0000702	enlarged lymph nodes	Nt5c3<em1(IMPC)Tcp>/Nt5c3<em1(IMPC)Tcp>	C57BL/6NCrl-Nt5c3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414989	F	MP:0002092	abnormal eye morphology	Nt5c3<em1(IMPC)Tcp>/Nt5c3<em1(IMPC)Tcp>	C57BL/6NCrl-Nt5c3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414989	M	MP:0000157	abnormal sternum morphology	Nt5c3<em1(IMPC)Tcp>/Nt5c3<em1(IMPC)Tcp>	C57BL/6NCrl-Nt5c3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414990	M	MP:0000266	abnormal heart morphology	Nt5e<em1(IMPC)Mbp>/Nt5e<em1(IMPC)Mbp>	C57BL/6NCrl-Nt5e<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414990	F	MP:0002989	small kidney	Nt5e<em1(IMPC)Mbp>/Nt5e<em1(IMPC)Mbp>	C57BL/6NCrl-Nt5e<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414990	F	MP:0002092	abnormal eye morphology	Nt5e<em1(IMPC)Mbp>/Nt5e<em1(IMPC)Mbp>	C57BL/6NCrl-Nt5e<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414990	M	MP:0001304	cataract	Nt5e<em1(IMPC)Mbp>/Nt5e<em1(IMPC)Mbp>	C57BL/6NCrl-Nt5e<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414990	M	MP:0001146	abnormal testis morphology	Nt5e<em1(IMPC)Mbp>/Nt5e<em1(IMPC)Mbp>	C57BL/6NCrl-Nt5e<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414990	M	MP:0009552	urinary bladder obstruction	Nt5e<em1(IMPC)Mbp>/Nt5e<em1(IMPC)Mbp>	C57BL/6NCrl-Nt5e<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414990	M	MP:0000691	enlarged spleen	Nt5e<em1(IMPC)Mbp>/Nt5e<em1(IMPC)Mbp>	C57BL/6NCrl-Nt5e<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414990	M	MP:0000274	enlarged heart	Nt5e<em1(IMPC)Mbp>/Nt5e<em1(IMPC)Mbp>	C57BL/6NCrl-Nt5e<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414990	M	MP:0003068	enlarged kidney	Nt5e<em1(IMPC)Mbp>/Nt5e<em1(IMPC)Mbp>	C57BL/6NCrl-Nt5e<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414990	M	MP:0000689	abnormal spleen morphology	Nt5e<em1(IMPC)Mbp>/Nt5e<em1(IMPC)Mbp>	C57BL/6NCrl-Nt5e<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414990	M	MP:0001148	enlarged testis	Nt5e<em1(IMPC)Mbp>/Nt5e<em1(IMPC)Mbp>	C57BL/6NCrl-Nt5e<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414991	F	MP:0000691	enlarged spleen	Nthl1<em1(IMPC)Mbp>/Nthl1<em1(IMPC)Mbp>	C57BL/6NCrl-Nthl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414991	F	MP:0000689	abnormal spleen morphology	Nthl1<em1(IMPC)Mbp>/Nthl1<em1(IMPC)Mbp>	C57BL/6NCrl-Nthl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414991	F	MP:0000601	small liver	Nthl1<em1(IMPC)Mbp>/Nthl1<em1(IMPC)Mbp>	C57BL/6NCrl-Nthl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414991	F	MP:0000598	abnormal liver morphology	Nthl1<em1(IMPC)Mbp>/Nthl1<em1(IMPC)Mbp>	C57BL/6NCrl-Nthl1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414992	M	MP:0000274	enlarged heart	Nuggc<em1(IMPC)Ccpcz>/Nuggc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nuggc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414992	M	MP:0000759	abnormal skeletal muscle morphology	Nuggc<em1(IMPC)Ccpcz>/Nuggc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nuggc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414992	F	MP:0000703	abnormal thymus morphology	Nuggc<em1(IMPC)Ccpcz>/Nuggc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nuggc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414992	F	MP:0000709	enlarged thymus	Nuggc<em1(IMPC)Ccpcz>/Nuggc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nuggc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414992	M	MP:0002059	abnormal seminal vesicle morphology	Nuggc<em1(IMPC)Ccpcz>/Nuggc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nuggc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414992	M	MP:0000266	abnormal heart morphology	Nuggc<em1(IMPC)Ccpcz>/Nuggc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nuggc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7414993	F	MP:0000598	abnormal liver morphology	Nup210<em1(IMPC)Mbp>/Nup210<em1(IMPC)Mbp>	C57BL/6NCrl-Nup210<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414993	F	MP:0000601	small liver	Nup210<em1(IMPC)Mbp>/Nup210<em1(IMPC)Mbp>	C57BL/6NCrl-Nup210<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7414994	M	MP:0002060	abnormal skin morphology	Osbp<em1(IMPC)Tcp>/Osbp<+>	C57BL/6NCrl-Osbp<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414994	M	MP:0000157	abnormal sternum morphology	Osbp<em1(IMPC)Tcp>/Osbp<+>	C57BL/6NCrl-Osbp<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414994	M	MP:0005562	decreased mean corpuscular hemoglobin	Osbp<em1(IMPC)Tcp>/Osbp<+>	C57BL/6NCrl-Osbp<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414994	M	MP:0000702	enlarged lymph nodes	Osbp<em1(IMPC)Tcp>/Osbp<+>	C57BL/6NCrl-Osbp<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414996	M	MP:0001304	cataract	Osbpl8<em1(IMPC)Tcp>/Osbpl8<em1(IMPC)Tcp>	C57BL/6NCrl-Osbpl8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414996	F	MP:0020870	decreased thigmotaxis	Osbpl8<em1(IMPC)Tcp>/Osbpl8<em1(IMPC)Tcp>	C57BL/6NCrl-Osbpl8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414996	M	MP:0001303	abnormal lens morphology	Osbpl8<em1(IMPC)Tcp>/Osbpl8<em1(IMPC)Tcp>	C57BL/6NCrl-Osbpl8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414996	M	MP:0000157	abnormal sternum morphology	Osbpl8<em1(IMPC)Tcp>/Osbpl8<em1(IMPC)Tcp>	C57BL/6NCrl-Osbpl8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414996	F	MP:0002092	abnormal eye morphology	Osbpl8<em1(IMPC)Tcp>/Osbpl8<em1(IMPC)Tcp>	C57BL/6NCrl-Osbpl8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414997	F	MP:0002941	increased circulating alanine transaminase level	Pacsin1<em1(IMPC)H>/Pacsin1<em1(IMPC)H>	C57BL/6NTac-Pacsin1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7414998	M	MP:0005505	thrombocytosis	Paip1<em1(IMPC)Tcp>/Paip1<em1(IMPC)Tcp>	C57BL/6NCrl-Paip1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414998	M	MP:0000702	enlarged lymph nodes	Paip1<em1(IMPC)Tcp>/Paip1<em1(IMPC)Tcp>	C57BL/6NCrl-Paip1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414998	M	MP:0001925	male infertility	Paip1<em1(IMPC)Tcp>/Paip1<em1(IMPC)Tcp>	C57BL/6NCrl-Paip1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414998	M	MP:0000208	decreased hematocrit	Paip1<em1(IMPC)Tcp>/Paip1<em1(IMPC)Tcp>	C57BL/6NCrl-Paip1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414998	M	MP:0005419	decreased circulating serum albumin level	Paip1<em1(IMPC)Tcp>/Paip1<em1(IMPC)Tcp>	C57BL/6NCrl-Paip1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414998	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Paip1<em1(IMPC)Tcp>/Paip1<em1(IMPC)Tcp>	C57BL/6NCrl-Paip1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414998	M	MP:0010067	increased red blood cell distribution width	Paip1<em1(IMPC)Tcp>/Paip1<em1(IMPC)Tcp>	C57BL/6NCrl-Paip1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7414999	M	MP:0000470	abnormal stomach morphology	Pals2<em1(IMPC)Rbrc>/Pals2<em1(IMPC)Rbrc>	C57BL/6NJcl-Pals2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414999	F	MP:0003795	abnormal bone structure	Pals2<em1(IMPC)Rbrc>/Pals2<em1(IMPC)Rbrc>	C57BL/6NJcl-Pals2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7414999	M	MP:0000689	abnormal spleen morphology	Pals2<em1(IMPC)Rbrc>/Pals2<em1(IMPC)Rbrc>	C57BL/6NJcl-Pals2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415001	M	MP:0002060	abnormal skin morphology	Pcnt<em1(IMPC)Mbp>/Pcnt<+>	C57BL/6NCrl-Pcnt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415001	M	MP:0002699	abnormal vitreous body morphology	Pcnt<em1(IMPC)Mbp>/Pcnt<+>	C57BL/6NCrl-Pcnt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415001	F	MP:0002092	abnormal eye morphology	Pcnt<em1(IMPC)Mbp>/Pcnt<+>	C57BL/6NCrl-Pcnt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415001	M	MP:0001147	small testis	Pcnt<em1(IMPC)Mbp>/Pcnt<+>	C57BL/6NCrl-Pcnt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415001	F	MP:0001289	persistence of hyaloid vascular system	Pcnt<em1(IMPC)Mbp>/Pcnt<+>	C57BL/6NCrl-Pcnt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415001	M	MP:0002135	abnormal kidney morphology	Pcnt<em1(IMPC)Mbp>/Pcnt<+>	C57BL/6NCrl-Pcnt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415001	F	MP:0001293	anophthalmia	Pcnt<em1(IMPC)Mbp>/Pcnt<+>	C57BL/6NCrl-Pcnt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415001	M	MP:0001146	abnormal testis morphology	Pcnt<em1(IMPC)Mbp>/Pcnt<+>	C57BL/6NCrl-Pcnt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415001	M	MP:0001304	cataract	Pcnt<em1(IMPC)Mbp>/Pcnt<+>	C57BL/6NCrl-Pcnt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415001	M	MP:0002989	small kidney	Pcnt<em1(IMPC)Mbp>/Pcnt<+>	C57BL/6NCrl-Pcnt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415001	F	MP:0001258	decreased body length	Pcnt<em1(IMPC)Mbp>/Pcnt<+>	C57BL/6NCrl-Pcnt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415002	M	MP:0001297	microphthalmia	Pcnt<em1(IMPC)Mbp>/Pcnt<em1(IMPC)Mbp>	C57BL/6NCrl-Pcnt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415002	M	MP:0003984	embryonic growth retardation	Pcnt<em1(IMPC)Mbp>/Pcnt<em1(IMPC)Mbp>	C57BL/6NCrl-Pcnt<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415003	M	MP:0001402	decreased locomotor activity	Pcp4l1<tm1b(KOMP)Wtsi>/Pcp4l1<tm1b(KOMP)Wtsi>	C57BL/6NCrl-Pcp4l1<tm1b(KOMP)Wtsi>/Ccpcz	N	MGI:5576271
MGI:7415004	F	MP:0002590	increased mean corpuscular volume	Pde10a<em1(IMPC)H>/Pde10a<em1(IMPC)H>	C57BL/6NTac-Pde10a<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415004	F	MP:0002599	increased mean platelet volume	Pde10a<em1(IMPC)H>/Pde10a<em1(IMPC)H>	C57BL/6NTac-Pde10a<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415004	F	MP:0008810	increased circulating iron level	Pde10a<em1(IMPC)H>/Pde10a<em1(IMPC)H>	C57BL/6NTac-Pde10a<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415005	F	MP:0000367	abnormal coat/ hair morphology	Pdia3<em1(IMPC)Hmgu>/Pdia3<+>	C57BL/6NCrl-Pdia3<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415007	F	MP:0001304	cataract	Pdp2<em1(IMPC)J>/Pdp2<em1(IMPC)J>	C57BL/6NJ-Pdp2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415009	M	MP:0000266	abnormal heart morphology	Pglyrp4<em1(IMPC)Ccpcz>/Pglyrp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pglyrp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415009	M	MP:0000274	enlarged heart	Pglyrp4<em1(IMPC)Ccpcz>/Pglyrp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pglyrp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415009	M	MP:0000706	small thymus	Pglyrp4<em1(IMPC)Ccpcz>/Pglyrp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pglyrp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415009	M	MP:0000691	enlarged spleen	Pglyrp4<em1(IMPC)Ccpcz>/Pglyrp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pglyrp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415009	F	MP:0000709	enlarged thymus	Pglyrp4<em1(IMPC)Ccpcz>/Pglyrp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pglyrp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415011	M	MP:0001148	enlarged testis	Pi16<em1(IMPC)Mbp>/Pi16<em1(IMPC)Mbp>	C57BL/6NCrl-Pi16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415011	M	MP:0000689	abnormal spleen morphology	Pi16<em1(IMPC)Mbp>/Pi16<em1(IMPC)Mbp>	C57BL/6NCrl-Pi16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415011	M	MP:0000691	enlarged spleen	Pi16<em1(IMPC)Mbp>/Pi16<em1(IMPC)Mbp>	C57BL/6NCrl-Pi16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415011	F	MP:0002989	small kidney	Pi16<em1(IMPC)Mbp>/Pi16<em1(IMPC)Mbp>	C57BL/6NCrl-Pi16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415011	F	MP:0005344	increased circulating bilirubin level	Pi16<em1(IMPC)Mbp>/Pi16<em1(IMPC)Mbp>	C57BL/6NCrl-Pi16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415011	F	MP:0002135	abnormal kidney morphology	Pi16<em1(IMPC)Mbp>/Pi16<em1(IMPC)Mbp>	C57BL/6NCrl-Pi16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415011	M	MP:0001146	abnormal testis morphology	Pi16<em1(IMPC)Mbp>/Pi16<em1(IMPC)Mbp>	C57BL/6NCrl-Pi16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415011	M	MP:0000062	increased bone mineral density	Pi16<em1(IMPC)Mbp>/Pi16<em1(IMPC)Mbp>	C57BL/6NCrl-Pi16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415012	F	MP:0001297	microphthalmia	Pla2g2f<em1(IMPC)Ccpcz>/Pla2g2f<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g2f<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415012	M	MP:0001262	decreased body weight	Pla2g2f<em1(IMPC)Ccpcz>/Pla2g2f<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g2f<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415012	M	MP:0001147	small testis	Pla2g2f<em1(IMPC)Ccpcz>/Pla2g2f<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g2f<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415012	F	MP:0002092	abnormal eye morphology	Pla2g2f<em1(IMPC)Ccpcz>/Pla2g2f<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g2f<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415012	M	MP:0001146	abnormal testis morphology	Pla2g2f<em1(IMPC)Ccpcz>/Pla2g2f<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g2f<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415013	M	MP:0011874	enlarged urinary bladder	Plekha5<em1(IMPC)Tcp>/Plekha5<em1(IMPC)Tcp>	C57BL/6NCrl-Plekha5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415013	M	MP:0005562	decreased mean corpuscular hemoglobin	Plekha5<em1(IMPC)Tcp>/Plekha5<em1(IMPC)Tcp>	C57BL/6NCrl-Plekha5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415013	M	MP:0000702	enlarged lymph nodes	Plekha5<em1(IMPC)Tcp>/Plekha5<em1(IMPC)Tcp>	C57BL/6NCrl-Plekha5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415013	F	MP:0001488	increased startle reflex	Plekha5<em1(IMPC)Tcp>/Plekha5<em1(IMPC)Tcp>	C57BL/6NCrl-Plekha5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415013	M	MP:0002060	abnormal skin morphology	Plekha5<em1(IMPC)Tcp>/Plekha5<em1(IMPC)Tcp>	C57BL/6NCrl-Plekha5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415013	M	MP:0006241	abnormal placement of pupils	Plekha5<em1(IMPC)Tcp>/Plekha5<em1(IMPC)Tcp>	C57BL/6NCrl-Plekha5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415013	M	MP:0004952	increased spleen weight	Plekha5<em1(IMPC)Tcp>/Plekha5<em1(IMPC)Tcp>	C57BL/6NCrl-Plekha5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415014	M	MP:0005178	increased circulating cholesterol level	Pllp<tm1(KOMP)Vlcg>/Pllp<tm1(KOMP)Vlcg>	C57BL/6NCrl-Pllp<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7415014	M	MP:0001304	cataract	Pllp<tm1(KOMP)Vlcg>/Pllp<tm1(KOMP)Vlcg>	C57BL/6NCrl-Pllp<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7415014	M	MP:0001146	abnormal testis morphology	Pllp<tm1(KOMP)Vlcg>/Pllp<tm1(KOMP)Vlcg>	C57BL/6NCrl-Pllp<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7415014	M	MP:0002060	abnormal skin morphology	Pllp<tm1(KOMP)Vlcg>/Pllp<tm1(KOMP)Vlcg>	C57BL/6NCrl-Pllp<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7415014	M	MP:0002965	increased circulating serum albumin level	Pllp<tm1(KOMP)Vlcg>/Pllp<tm1(KOMP)Vlcg>	C57BL/6NCrl-Pllp<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7415014	M	MP:0002699	abnormal vitreous body morphology	Pllp<tm1(KOMP)Vlcg>/Pllp<tm1(KOMP)Vlcg>	C57BL/6NCrl-Pllp<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7415014	M	MP:0001148	enlarged testis	Pllp<tm1(KOMP)Vlcg>/Pllp<tm1(KOMP)Vlcg>	C57BL/6NCrl-Pllp<tm1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7415015	F	MP:0001258	decreased body length	Plxna4<em1(IMPC)Mbp>/Plxna4<em1(IMPC)Mbp>	C57BL/6NCrl-Plxna4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415015	F	MP:0000598	abnormal liver morphology	Plxna4<em1(IMPC)Mbp>/Plxna4<em1(IMPC)Mbp>	C57BL/6NCrl-Plxna4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415015	M	MP:0000689	abnormal spleen morphology	Plxna4<em1(IMPC)Mbp>/Plxna4<em1(IMPC)Mbp>	C57BL/6NCrl-Plxna4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415015	M	MP:0008259	abnormal optic disk morphology	Plxna4<em1(IMPC)Mbp>/Plxna4<em1(IMPC)Mbp>	C57BL/6NCrl-Plxna4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415015	F	MP:0001415	increased exploration in new environment	Plxna4<em1(IMPC)Mbp>/Plxna4<em1(IMPC)Mbp>	C57BL/6NCrl-Plxna4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415015	F	MP:0002699	abnormal vitreous body morphology	Plxna4<em1(IMPC)Mbp>/Plxna4<em1(IMPC)Mbp>	C57BL/6NCrl-Plxna4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415015	F	MP:0001289	persistence of hyaloid vascular system	Plxna4<em1(IMPC)Mbp>/Plxna4<em1(IMPC)Mbp>	C57BL/6NCrl-Plxna4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415015	F	MP:0000601	small liver	Plxna4<em1(IMPC)Mbp>/Plxna4<em1(IMPC)Mbp>	C57BL/6NCrl-Plxna4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415015	F	MP:0001399	hyperactivity	Plxna4<em1(IMPC)Mbp>/Plxna4<em1(IMPC)Mbp>	C57BL/6NCrl-Plxna4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415015	M	MP:0001148	enlarged testis	Plxna4<em1(IMPC)Mbp>/Plxna4<em1(IMPC)Mbp>	C57BL/6NCrl-Plxna4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415015	M	MP:0001146	abnormal testis morphology	Plxna4<em1(IMPC)Mbp>/Plxna4<em1(IMPC)Mbp>	C57BL/6NCrl-Plxna4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415015	M	MP:0000692	small spleen	Plxna4<em1(IMPC)Mbp>/Plxna4<em1(IMPC)Mbp>	C57BL/6NCrl-Plxna4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415015	F	MP:0005278	abnormal cholesterol homeostasis	Plxna4<em1(IMPC)Mbp>/Plxna4<em1(IMPC)Mbp>	C57BL/6NCrl-Plxna4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415016	M	MP:0001552	increased circulating triglyceride level	Pm20d1<em1(IMPC)H>/Pm20d1<em1(IMPC)H>	C57BL/6NTac-Pm20d1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415016	M	MP:0001566	increased circulating phosphate level	Pm20d1<em1(IMPC)H>/Pm20d1<em1(IMPC)H>	C57BL/6NTac-Pm20d1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415016	F	MP:0002608	increased hematocrit	Pm20d1<em1(IMPC)H>/Pm20d1<em1(IMPC)H>	C57BL/6NTac-Pm20d1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415017	F	MP:0008820	abnormal blood uric acid level	Pnma3<em1(IMPC)Rbrc>/Pnma3<em1(IMPC)Rbrc>	C57BL/6NJcl-Pnma3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415018	M	MP:0005293	impaired glucose tolerance	Pomc<em1(IMPC)Rbrc>/Pomc<+>	C57BL/6NJcl-Pomc<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415018	F	MP:0000689	abnormal spleen morphology	Pomc<em1(IMPC)Rbrc>/Pomc<+>	C57BL/6NJcl-Pomc<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415018	F	MP:0000691	enlarged spleen	Pomc<em1(IMPC)Rbrc>/Pomc<+>	C57BL/6NJcl-Pomc<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415020	M	MP:0001312	abnormal cornea morphology	Ppat<em1(IMPC)Tcp>/Ppat<+>	C57BL/6NCrl-Ppat<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415020	M	MP:0000157	abnormal sternum morphology	Ppat<em1(IMPC)Tcp>/Ppat<+>	C57BL/6NCrl-Ppat<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415020	F	MP:0001303	abnormal lens morphology	Ppat<em1(IMPC)Tcp>/Ppat<+>	C57BL/6NCrl-Ppat<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415022	F	MP:0002135	abnormal kidney morphology	Ppia<em1(IMPC)Mbp>/Ppia<em1(IMPC)Mbp>	C57BL/6NCrl-Ppia<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415022	F	MP:0002989	small kidney	Ppia<em1(IMPC)Mbp>/Ppia<em1(IMPC)Mbp>	C57BL/6NCrl-Ppia<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415022	F	MP:0002731	megacolon	Ppia<em1(IMPC)Mbp>/Ppia<em1(IMPC)Mbp>	C57BL/6NCrl-Ppia<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415022	F	MP:0002968	increased circulating alkaline phosphatase level	Ppia<em1(IMPC)Mbp>/Ppia<em1(IMPC)Mbp>	C57BL/6NCrl-Ppia<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415022	M	MP:0002092	abnormal eye morphology	Ppia<em1(IMPC)Mbp>/Ppia<em1(IMPC)Mbp>	C57BL/6NCrl-Ppia<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415022	F	MP:0002875	decreased erythrocyte cell number	Ppia<em1(IMPC)Mbp>/Ppia<em1(IMPC)Mbp>	C57BL/6NCrl-Ppia<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415022	F	MP:0000495	abnormal colon morphology	Ppia<em1(IMPC)Mbp>/Ppia<em1(IMPC)Mbp>	C57BL/6NCrl-Ppia<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415022	M	MP:0001297	microphthalmia	Ppia<em1(IMPC)Mbp>/Ppia<em1(IMPC)Mbp>	C57BL/6NCrl-Ppia<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415022	F	MP:0005565	increased blood urea nitrogen level	Ppia<em1(IMPC)Mbp>/Ppia<em1(IMPC)Mbp>	C57BL/6NCrl-Ppia<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415023	M	MP:0001552	increased circulating triglyceride level	Ppme1<em1(IMPC)Rbrc>/Ppme1<+>	C57BL/6NJcl-Ppme1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415023	F	MP:0000598	abnormal liver morphology	Ppme1<em1(IMPC)Rbrc>/Ppme1<+>	C57BL/6NJcl-Ppme1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415025	F	MP:0002599	increased mean platelet volume	Ppp2r3c<em1(IMPC)H>/Ppp2r3c<+>	C57BL/6NTac-Ppp2r3c<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415027	M	MP:0002059	abnormal seminal vesicle morphology	Proser2<em1(IMPC)Ccpcz>/Proser2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Proser2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415027	F	MP:0000691	enlarged spleen	Proser2<em1(IMPC)Ccpcz>/Proser2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Proser2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415027	F	MP:0000689	abnormal spleen morphology	Proser2<em1(IMPC)Ccpcz>/Proser2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Proser2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415027	M	MP:0000702	enlarged lymph nodes	Proser2<em1(IMPC)Ccpcz>/Proser2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Proser2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415027	M	MP:0011625	cystolithiasis	Proser2<em1(IMPC)Ccpcz>/Proser2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Proser2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415027	F	MP:0000709	enlarged thymus	Proser2<em1(IMPC)Ccpcz>/Proser2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Proser2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415027	F	MP:0000703	abnormal thymus morphology	Proser2<em1(IMPC)Ccpcz>/Proser2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Proser2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415027	M	MP:0001489	decreased startle reflex	Proser2<em1(IMPC)Ccpcz>/Proser2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Proser2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415027	M	MP:0002339	abnormal lymph node morphology	Proser2<em1(IMPC)Ccpcz>/Proser2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Proser2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415027	M	MP:0000538	abnormal urinary bladder morphology	Proser2<em1(IMPC)Ccpcz>/Proser2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Proser2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415028	M	MP:0005562	decreased mean corpuscular hemoglobin	Prpf39<em1(IMPC)Tcp>/Prpf39<+>	C57BL/6NCrl-Prpf39<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415028	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Prpf39<em1(IMPC)Tcp>/Prpf39<+>	C57BL/6NCrl-Prpf39<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415028	F	MP:0002092	abnormal eye morphology	Prpf39<em1(IMPC)Tcp>/Prpf39<+>	C57BL/6NCrl-Prpf39<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415030	F	MP:0000703	abnormal thymus morphology	Prss48<em1(IMPC)Ccpcz>/Prss48<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss48<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415030	M	MP:0002059	abnormal seminal vesicle morphology	Prss48<em1(IMPC)Ccpcz>/Prss48<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss48<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415030	F	MP:0002110	abnormal digit morphology	Prss48<em1(IMPC)Ccpcz>/Prss48<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss48<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415030	F	MP:0002092	abnormal eye morphology	Prss48<em1(IMPC)Ccpcz>/Prss48<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss48<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415030	F	MP:0000709	enlarged thymus	Prss48<em1(IMPC)Ccpcz>/Prss48<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss48<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415030	M	MP:0003961	decreased lean body mass	Prss48<em1(IMPC)Ccpcz>/Prss48<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss48<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415030	M	MP:0002135	abnormal kidney morphology	Prss48<em1(IMPC)Ccpcz>/Prss48<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss48<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415030	F	MP:0000689	abnormal spleen morphology	Prss48<em1(IMPC)Ccpcz>/Prss48<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss48<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415030	M	MP:0010379	decreased respiratory quotient	Prss48<em1(IMPC)Ccpcz>/Prss48<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss48<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415030	M	MP:0001157	small seminal vesicle	Prss48<em1(IMPC)Ccpcz>/Prss48<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss48<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415031	M	MP:0001417	decreased exploration in new environment	Prss55<em1(IMPC)Ccpcz>/Prss55<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss55<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415031	F	MP:0002060	abnormal skin morphology	Prss55<em1(IMPC)Ccpcz>/Prss55<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss55<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415031	F	MP:0000691	enlarged spleen	Prss55<em1(IMPC)Ccpcz>/Prss55<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss55<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415031	M	MP:0001148	enlarged testis	Prss55<em1(IMPC)Ccpcz>/Prss55<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss55<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415031	M	MP:0001146	abnormal testis morphology	Prss55<em1(IMPC)Ccpcz>/Prss55<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss55<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415031	M	MP:0002059	abnormal seminal vesicle morphology	Prss55<em1(IMPC)Ccpcz>/Prss55<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss55<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415031	M	MP:0005333	decreased heart rate	Prss55<em1(IMPC)Ccpcz>/Prss55<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss55<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415031	M	MP:0002997	enlarged seminal vesicle	Prss55<em1(IMPC)Ccpcz>/Prss55<em1(IMPC)Ccpcz>	C57BL/6NCrl-Prss55<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415032	M	MP:0002059	abnormal seminal vesicle morphology	Psen2<em1(IMPC)Ccpcz>/Psen2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psen2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415032	F	MP:0000709	enlarged thymus	Psen2<em1(IMPC)Ccpcz>/Psen2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psen2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415032	F	MP:0000266	abnormal heart morphology	Psen2<em1(IMPC)Ccpcz>/Psen2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psen2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415032	F	MP:0000703	abnormal thymus morphology	Psen2<em1(IMPC)Ccpcz>/Psen2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psen2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415032	M	MP:0002152	abnormal brain morphology	Psen2<em1(IMPC)Ccpcz>/Psen2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psen2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415032	M	MP:0001891	hydrocephaly	Psen2<em1(IMPC)Ccpcz>/Psen2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psen2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415033	F	MP:0002100	abnormal tooth morphology	Ptbp2<em1(IMPC)Hmgu>/Ptbp2<+>	C57BL/6NCrl-Ptbp2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415033	F	MP:0002098	abnormal vibrissa morphology	Ptbp2<em1(IMPC)Hmgu>/Ptbp2<+>	C57BL/6NCrl-Ptbp2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415035	F	MP:0002060	abnormal skin morphology	Ptchd4<em1(IMPC)Ccpcz>/Ptchd4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ptchd4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415035	M	MP:0000266	abnormal heart morphology	Ptchd4<em1(IMPC)Ccpcz>/Ptchd4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ptchd4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415035	M	MP:0000274	enlarged heart	Ptchd4<em1(IMPC)Ccpcz>/Ptchd4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ptchd4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415035	F	MP:0011044	increased lung elastance	Ptchd4<em1(IMPC)Ccpcz>/Ptchd4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ptchd4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415036	M	MP:0010090	increased circulating creatine kinase level	Ptprm<em1(IMPC)Rbrc>/Ptprm<em1(IMPC)Rbrc>	C57BL/6NJcl-Ptprm<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415036	M	MP:0000266	abnormal heart morphology	Ptprm<em1(IMPC)Rbrc>/Ptprm<em1(IMPC)Rbrc>	C57BL/6NJcl-Ptprm<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415036	M	MP:0000274	enlarged heart	Ptprm<em1(IMPC)Rbrc>/Ptprm<em1(IMPC)Rbrc>	C57BL/6NJcl-Ptprm<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415037	M	MP:0000691	enlarged spleen	Pum1<em1(IMPC)Mbp>/Pum1<em1(IMPC)Mbp>	C57BL/6NCrl-Pum1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415037	M	MP:0000689	abnormal spleen morphology	Pum1<em1(IMPC)Mbp>/Pum1<em1(IMPC)Mbp>	C57BL/6NCrl-Pum1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415037	F	MP:0002060	abnormal skin morphology	Pum1<em1(IMPC)Mbp>/Pum1<em1(IMPC)Mbp>	C57BL/6NCrl-Pum1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415039	F	MP:0005562	decreased mean corpuscular hemoglobin	Pygm<em1(IMPC)J>/Pygm<em1(IMPC)J>	C57BL/6NJ-Pygm<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415039	F	MP:0010053	decreased grip strength	Pygm<em1(IMPC)J>/Pygm<em1(IMPC)J>	C57BL/6NJ-Pygm<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415039	F	MP:0001402	decreased locomotor activity	Pygm<em1(IMPC)J>/Pygm<em1(IMPC)J>	C57BL/6NJ-Pygm<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415039	M	MP:0010506	prolonged RR interval	Pygm<em1(IMPC)J>/Pygm<em1(IMPC)J>	C57BL/6NJ-Pygm<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415039	F	MP:0002968	increased circulating alkaline phosphatase level	Pygm<em1(IMPC)J>/Pygm<em1(IMPC)J>	C57BL/6NJ-Pygm<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415040	F	MP:0001297	microphthalmia	Rab11fip2<em1(IMPC)Mbp>/Rab11fip2<em1(IMPC)Mbp>	C57BL/6NCrl-Rab11fip2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415040	M	MP:0001148	enlarged testis	Rab11fip2<em1(IMPC)Mbp>/Rab11fip2<em1(IMPC)Mbp>	C57BL/6NCrl-Rab11fip2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415040	F	MP:0002092	abnormal eye morphology	Rab11fip2<em1(IMPC)Mbp>/Rab11fip2<em1(IMPC)Mbp>	C57BL/6NCrl-Rab11fip2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415040	F	MP:0000702	enlarged lymph nodes	Rab11fip2<em1(IMPC)Mbp>/Rab11fip2<em1(IMPC)Mbp>	C57BL/6NCrl-Rab11fip2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415040	F	MP:0002339	abnormal lymph node morphology	Rab11fip2<em1(IMPC)Mbp>/Rab11fip2<em1(IMPC)Mbp>	C57BL/6NCrl-Rab11fip2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415040	M	MP:0001146	abnormal testis morphology	Rab11fip2<em1(IMPC)Mbp>/Rab11fip2<em1(IMPC)Mbp>	C57BL/6NCrl-Rab11fip2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415041	F	MP:0001392	abnormal locomotor behavior	Rab26<em1(IMPC)H>/Rab26<em1(IMPC)H>	C57BL/6NTac-Rab26<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415042	M	MP:0011874	enlarged urinary bladder	Rad54l2<em1(IMPC)Tcp>/Rad54l2<+>	C57BL/6NCrl-Rad54l2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415042	M	MP:0005505	thrombocytosis	Rad54l2<em1(IMPC)Tcp>/Rad54l2<+>	C57BL/6NCrl-Rad54l2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415042	M	MP:0003960	increased lean body mass	Rad54l2<em1(IMPC)Tcp>/Rad54l2<+>	C57BL/6NCrl-Rad54l2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415042	M	MP:0002060	abnormal skin morphology	Rad54l2<em1(IMPC)Tcp>/Rad54l2<+>	C57BL/6NCrl-Rad54l2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415042	M	MP:0000157	abnormal sternum morphology	Rad54l2<em1(IMPC)Tcp>/Rad54l2<+>	C57BL/6NCrl-Rad54l2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415044	M	MP:0003604	single kidney	Rfk<em1(IMPC)Mbp>/Rfk<+>	C57BL/6NCrl-Rfk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415044	M	MP:0001146	abnormal testis morphology	Rfk<em1(IMPC)Mbp>/Rfk<+>	C57BL/6NCrl-Rfk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415044	M	MP:0000692	small spleen	Rfk<em1(IMPC)Mbp>/Rfk<+>	C57BL/6NCrl-Rfk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415044	M	MP:0000689	abnormal spleen morphology	Rfk<em1(IMPC)Mbp>/Rfk<+>	C57BL/6NCrl-Rfk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415044	M	MP:0001148	enlarged testis	Rfk<em1(IMPC)Mbp>/Rfk<+>	C57BL/6NCrl-Rfk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415046	M	MP:0001589	abnormal mean corpuscular hemoglobin	Rlim<em1(IMPC)Rbrc>/Y	C57BL/6NJcl-Rlim<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415046	M	MP:0004613	fusion of vertebral arches	Rlim<em1(IMPC)Rbrc>/Y	C57BL/6NJcl-Rlim<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415046	M	MP:0000226	abnormal mean corpuscular volume	Rlim<em1(IMPC)Rbrc>/Y	C57BL/6NJcl-Rlim<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415047	F	MP:0000709	enlarged thymus	Rlim<em1(IMPC)Rbrc>/Rlim<+>	C57BL/6NJcl-Rlim<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415047	F	MP:0002339	abnormal lymph node morphology	Rlim<em1(IMPC)Rbrc>/Rlim<+>	C57BL/6NJcl-Rlim<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415047	F	MP:0000703	abnormal thymus morphology	Rlim<em1(IMPC)Rbrc>/Rlim<+>	C57BL/6NJcl-Rlim<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415047	F	MP:0000702	enlarged lymph nodes	Rlim<em1(IMPC)Rbrc>/Rlim<+>	C57BL/6NJcl-Rlim<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415047	F	MP:0000274	enlarged heart	Rlim<em1(IMPC)Rbrc>/Rlim<+>	C57BL/6NJcl-Rlim<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415047	F	MP:0000266	abnormal heart morphology	Rlim<em1(IMPC)Rbrc>/Rlim<+>	C57BL/6NJcl-Rlim<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415048	F	MP:0001126	abnormal ovary morphology	Rnaseh2a<em1(IMPC)Tcp>/Rnaseh2a<+>	C57BL/6NCrl-Rnaseh2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415048	M	MP:0005505	thrombocytosis	Rnaseh2a<em1(IMPC)Tcp>/Rnaseh2a<+>	C57BL/6NCrl-Rnaseh2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415048	M	MP:0001488	increased startle reflex	Rnaseh2a<em1(IMPC)Tcp>/Rnaseh2a<+>	C57BL/6NCrl-Rnaseh2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415048	F	MP:0002599	increased mean platelet volume	Rnaseh2a<em1(IMPC)Tcp>/Rnaseh2a<+>	C57BL/6NCrl-Rnaseh2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415048	M	MP:0000220	increased monocyte cell number	Rnaseh2a<em1(IMPC)Tcp>/Rnaseh2a<+>	C57BL/6NCrl-Rnaseh2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415048	F	MP:0005562	decreased mean corpuscular hemoglobin	Rnaseh2a<em1(IMPC)Tcp>/Rnaseh2a<+>	C57BL/6NCrl-Rnaseh2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415048	M	MP:0004952	increased spleen weight	Rnaseh2a<em1(IMPC)Tcp>/Rnaseh2a<+>	C57BL/6NCrl-Rnaseh2a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415050	M	MP:0005564	increased hemoglobin content	Rnf43<em1(IMPC)Tcp>/Rnf43<em1(IMPC)Tcp>	C57BL/6NCrl-Rnf43<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415050	F	MP:0000691	enlarged spleen	Rnf43<em1(IMPC)Tcp>/Rnf43<em1(IMPC)Tcp>	C57BL/6NCrl-Rnf43<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415050	M	MP:0010025	decreased total body fat amount	Rnf43<em1(IMPC)Tcp>/Rnf43<em1(IMPC)Tcp>	C57BL/6NCrl-Rnf43<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415050	M	MP:0002060	abnormal skin morphology	Rnf43<em1(IMPC)Tcp>/Rnf43<em1(IMPC)Tcp>	C57BL/6NCrl-Rnf43<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415050	M	MP:0002608	increased hematocrit	Rnf43<em1(IMPC)Tcp>/Rnf43<em1(IMPC)Tcp>	C57BL/6NCrl-Rnf43<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415051	M	MP:0000538	abnormal urinary bladder morphology	Rras2<em1(IMPC)Ccpcz>/Rras2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rras2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415051	F	MP:0000709	enlarged thymus	Rras2<em1(IMPC)Ccpcz>/Rras2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rras2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415051	F	MP:0001120	abnormal uterus morphology	Rras2<em1(IMPC)Ccpcz>/Rras2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rras2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415051	F	MP:0009709	hydrometra	Rras2<em1(IMPC)Ccpcz>/Rras2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rras2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415051	F	MP:0002135	abnormal kidney morphology	Rras2<em1(IMPC)Ccpcz>/Rras2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rras2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415051	F	MP:0000703	abnormal thymus morphology	Rras2<em1(IMPC)Ccpcz>/Rras2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rras2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415053	M	MP:0010067	increased red blood cell distribution width	Rtn4rl2<em1(IMPC)Mbp>/Rtn4rl2<em1(IMPC)Mbp>	C57BL/6NCrl-Rtn4rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415053	F	MP:0000274	enlarged heart	Rtn4rl2<em1(IMPC)Mbp>/Rtn4rl2<em1(IMPC)Mbp>	C57BL/6NCrl-Rtn4rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415053	M	MP:0002699	abnormal vitreous body morphology	Rtn4rl2<em1(IMPC)Mbp>/Rtn4rl2<em1(IMPC)Mbp>	C57BL/6NCrl-Rtn4rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415053	M	MP:0003068	enlarged kidney	Rtn4rl2<em1(IMPC)Mbp>/Rtn4rl2<em1(IMPC)Mbp>	C57BL/6NCrl-Rtn4rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415053	M	MP:0001304	cataract	Rtn4rl2<em1(IMPC)Mbp>/Rtn4rl2<em1(IMPC)Mbp>	C57BL/6NCrl-Rtn4rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415053	M	MP:0001146	abnormal testis morphology	Rtn4rl2<em1(IMPC)Mbp>/Rtn4rl2<em1(IMPC)Mbp>	C57BL/6NCrl-Rtn4rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415053	M	MP:0002135	abnormal kidney morphology	Rtn4rl2<em1(IMPC)Mbp>/Rtn4rl2<em1(IMPC)Mbp>	C57BL/6NCrl-Rtn4rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415053	M	MP:0002152	abnormal brain morphology	Rtn4rl2<em1(IMPC)Mbp>/Rtn4rl2<em1(IMPC)Mbp>	C57BL/6NCrl-Rtn4rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415053	M	MP:0001147	small testis	Rtn4rl2<em1(IMPC)Mbp>/Rtn4rl2<em1(IMPC)Mbp>	C57BL/6NCrl-Rtn4rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415053	F	MP:0000266	abnormal heart morphology	Rtn4rl2<em1(IMPC)Mbp>/Rtn4rl2<em1(IMPC)Mbp>	C57BL/6NCrl-Rtn4rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415053	M	MP:0000774	decreased brain size	Rtn4rl2<em1(IMPC)Mbp>/Rtn4rl2<em1(IMPC)Mbp>	C57BL/6NCrl-Rtn4rl2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415054	F	MP:0003795	abnormal bone structure	Runx2<em1(IMPC)Rbrc>/Runx2<+>	C57BL/6NJcl-Runx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415054	M	MP:0005296	abnormal humerus morphology	Runx2<em1(IMPC)Rbrc>/Runx2<+>	C57BL/6NJcl-Runx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415054	F	MP:0010124	decreased bone mineral content	Runx2<em1(IMPC)Rbrc>/Runx2<+>	C57BL/6NJcl-Runx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415054	F	MP:0003960	increased lean body mass	Runx2<em1(IMPC)Rbrc>/Runx2<+>	C57BL/6NJcl-Runx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415054	M	MP:0001489	decreased startle reflex	Runx2<em1(IMPC)Rbrc>/Runx2<+>	C57BL/6NJcl-Runx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415055	M	MP:0002135	abnormal kidney morphology	Ryk<em1(IMPC)Mbp>/Ryk<+>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415055	M	MP:0000218	increased leukocyte cell number	Ryk<em1(IMPC)Mbp>/Ryk<+>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415055	F	MP:0001289	persistence of hyaloid vascular system	Ryk<em1(IMPC)Mbp>/Ryk<+>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415055	M	MP:0006203	eye hemorrhage	Ryk<em1(IMPC)Mbp>/Ryk<+>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415055	M	MP:0003068	enlarged kidney	Ryk<em1(IMPC)Mbp>/Ryk<+>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415055	F	MP:0000266	abnormal heart morphology	Ryk<em1(IMPC)Mbp>/Ryk<+>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415055	M	MP:0000220	increased monocyte cell number	Ryk<em1(IMPC)Mbp>/Ryk<+>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415055	F	MP:0002060	abnormal skin morphology	Ryk<em1(IMPC)Mbp>/Ryk<+>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415055	F	MP:0000274	enlarged heart	Ryk<em1(IMPC)Mbp>/Ryk<+>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415055	M	MP:0005013	increased lymphocyte cell number	Ryk<em1(IMPC)Mbp>/Ryk<+>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415055	F	MP:0000689	abnormal spleen morphology	Ryk<em1(IMPC)Mbp>/Ryk<+>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415055	F	MP:0000691	enlarged spleen	Ryk<em1(IMPC)Mbp>/Ryk<+>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415056	F	MP:0001711	abnormal placenta morphology	Ryk<em1(IMPC)Mbp>/Ryk<em1(IMPC)Mbp>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415056	F	MP:0000111	cleft palate	Ryk<em1(IMPC)Mbp>/Ryk<em1(IMPC)Mbp>	C57BL/6NCrl-Ryk<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415057	M	MP:0001523	impaired righting response	Samm50<em1(IMPC)Hmgu>/Samm50<+>	C57BL/6NCrl-Samm50<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415057	M	MP:0002100	abnormal tooth morphology	Samm50<em1(IMPC)Hmgu>/Samm50<+>	C57BL/6NCrl-Samm50<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415059	M	MP:0001146	abnormal testis morphology	Scml2<em1(IMPC)Rbrc>/Y	C57BL/6NJcl-Scml2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415059	M	MP:0001147	small testis	Scml2<em1(IMPC)Rbrc>/Y	C57BL/6NJcl-Scml2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415060	M	MP:0001891	hydrocephaly	Scube1<em1(IMPC)Rbrc>/Scube1<em1(IMPC)Rbrc>	C57BL/6NJcl-Scube1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415060	F	MP:0001926	female infertility	Scube1<em1(IMPC)Rbrc>/Scube1<em1(IMPC)Rbrc>	C57BL/6NJcl-Scube1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415060	M	MP:0001925	male infertility	Scube1<em1(IMPC)Rbrc>/Scube1<em1(IMPC)Rbrc>	C57BL/6NJcl-Scube1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415061	M	MP:0005553	increased circulating creatinine level	Sdc1<em1(IMPC)H>/Sdc1<em1(IMPC)H>	C57BL/6NTac-Sdc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415061	M	MP:0001556	increased circulating HDL cholesterol level	Sdc1<em1(IMPC)H>/Sdc1<em1(IMPC)H>	C57BL/6NTac-Sdc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415061	M	MP:0005178	increased circulating cholesterol level	Sdc1<em1(IMPC)H>/Sdc1<em1(IMPC)H>	C57BL/6NTac-Sdc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415061	F	MP:0005292	improved glucose tolerance	Sdc1<em1(IMPC)H>/Sdc1<em1(IMPC)H>	C57BL/6NTac-Sdc1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415062	F	MP:0002092	abnormal eye morphology	Sec24b<em1(IMPC)Tcp>/Sec24b<+>	C57BL/6NCrl-Sec24b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415062	M	MP:0000691	enlarged spleen	Sec24b<em1(IMPC)Tcp>/Sec24b<+>	C57BL/6NCrl-Sec24b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415062	M	MP:0000702	enlarged lymph nodes	Sec24b<em1(IMPC)Tcp>/Sec24b<+>	C57BL/6NCrl-Sec24b<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415064	M	MP:0000598	abnormal liver morphology	Sec24d<em1(IMPC)Rbrc>/Sec24d<+>	C57BL/6NJcl-Sec24d<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415064	M	MP:0000470	abnormal stomach morphology	Sec24d<em1(IMPC)Rbrc>/Sec24d<+>	C57BL/6NJcl-Sec24d<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415064	M	MP:0005293	impaired glucose tolerance	Sec24d<em1(IMPC)Rbrc>/Sec24d<+>	C57BL/6NJcl-Sec24d<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415066	M	MP:0002152	abnormal brain morphology	Selenot<em1(IMPC)Mbp>/Selenot<em1(IMPC)Mbp>	C57BL/6NCrl-Selenot<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415066	F	MP:0001489	decreased startle reflex	Selenot<em1(IMPC)Mbp>/Selenot<em1(IMPC)Mbp>	C57BL/6NCrl-Selenot<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415066	M	MP:0000774	decreased brain size	Selenot<em1(IMPC)Mbp>/Selenot<em1(IMPC)Mbp>	C57BL/6NCrl-Selenot<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415066	M	MP:0001402	decreased locomotor activity	Selenot<em1(IMPC)Mbp>/Selenot<em1(IMPC)Mbp>	C57BL/6NCrl-Selenot<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415066	M	MP:0002060	abnormal skin morphology	Selenot<em1(IMPC)Mbp>/Selenot<em1(IMPC)Mbp>	C57BL/6NCrl-Selenot<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415066	M	MP:0001146	abnormal testis morphology	Selenot<em1(IMPC)Mbp>/Selenot<em1(IMPC)Mbp>	C57BL/6NCrl-Selenot<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415066	M	MP:0001147	small testis	Selenot<em1(IMPC)Mbp>/Selenot<em1(IMPC)Mbp>	C57BL/6NCrl-Selenot<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415066	F	MP:0003795	abnormal bone structure	Selenot<em1(IMPC)Mbp>/Selenot<em1(IMPC)Mbp>	C57BL/6NCrl-Selenot<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415066	M	MP:0009141	increased prepulse inhibition	Selenot<em1(IMPC)Mbp>/Selenot<em1(IMPC)Mbp>	C57BL/6NCrl-Selenot<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415066	F	MP:0001258	decreased body length	Selenot<em1(IMPC)Mbp>/Selenot<em1(IMPC)Mbp>	C57BL/6NCrl-Selenot<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415067	F	MP:0001325	abnormal retina morphology	Sema3e<em1(IMPC)H>/Sema3e<em1(IMPC)H>	C57BL/6NTac-Sema3e<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415067	F	MP:0000198	decreased circulating phosphate level	Sema3e<em1(IMPC)H>/Sema3e<em1(IMPC)H>	C57BL/6NTac-Sema3e<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415067	F	MP:0006243	impaired pupillary reflex	Sema3e<em1(IMPC)H>/Sema3e<em1(IMPC)H>	C57BL/6NTac-Sema3e<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415067	M	MP:0010097	abnormal retina blood vessel morphology	Sema3e<em1(IMPC)H>/Sema3e<em1(IMPC)H>	C57BL/6NTac-Sema3e<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415068	M	MP:0002941	increased circulating alanine transaminase level	Septin14<em1(IMPC)Tcp>/Septin14<em1(IMPC)Tcp>	C57BL/6NCrl-Septin14<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415068	M	MP:0005343	increased circulating aspartate transaminase level	Septin14<em1(IMPC)Tcp>/Septin14<em1(IMPC)Tcp>	C57BL/6NCrl-Septin14<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415069	M	MP:0010052	increased grip strength	Serpina3i<em1(IMPC)J>/Serpina3i<em1(IMPC)J>	C57BL/6NJ-Serpina3i<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415069	F	MP:0000221	decreased leukocyte cell number	Serpina3i<em1(IMPC)J>/Serpina3i<em1(IMPC)J>	C57BL/6NJ-Serpina3i<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415070	M	MP:0002875	decreased erythrocyte cell number	Shank2<em2(IMPC)Rbrc>/Shank2<em2(IMPC)Rbrc>	C57BL/6NJcl-Shank2<em2(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415070	F	MP:0012440	abnormal neutrophil cell number	Shank2<em2(IMPC)Rbrc>/Shank2<em2(IMPC)Rbrc>	C57BL/6NJcl-Shank2<em2(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415072	M	MP:0009342	enlarged gallbladder	Slc15a5<em1(IMPC)H>/Slc15a5<em1(IMPC)H>	C57BL/6NTac-Slc15a5<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415073	F	MP:0002989	small kidney	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0001258	decreased body length	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0000470	abnormal stomach morphology	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0009483	enlarged ileum	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0001120	abnormal uterus morphology	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0005333	decreased heart rate	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0011503	distended jejunum	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0000706	small thymus	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0000703	abnormal thymus morphology	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	M	MP:0000599	enlarged liver	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	M	MP:0002059	abnormal seminal vesicle morphology	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0009476	enlarged cecum	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0000494	abnormal cecum morphology	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	M	MP:0002981	increased liver weight	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0011882	enlarged duodenum	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0002060	abnormal skin morphology	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0000495	abnormal colon morphology	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0001175	abnormal lung morphology	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0002152	abnormal brain morphology	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0002637	small uterus	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	M	MP:0001157	small seminal vesicle	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415073	F	MP:0010506	prolonged RR interval	Slc29a3<em1(IMPC)Mbp>/Slc29a3<em1(IMPC)Mbp>	C57BL/6NCrl-Slc29a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415074	F	MP:0005634	decreased circulating sodium level	Slc35f5<em1(IMPC)Hmgu>/Slc35f5<em1(IMPC)Hmgu>	C57BL/6NCrl-Slc35f5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415075	F	MP:0010123	increased bone mineral content	Slc37a2<em1(IMPC)Mbp>/Slc37a2<em1(IMPC)Mbp>	C57BL/6NCrl-Slc37a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415075	M	MP:0002339	abnormal lymph node morphology	Slc37a2<em1(IMPC)Mbp>/Slc37a2<em1(IMPC)Mbp>	C57BL/6NCrl-Slc37a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415075	M	MP:0001148	enlarged testis	Slc37a2<em1(IMPC)Mbp>/Slc37a2<em1(IMPC)Mbp>	C57BL/6NCrl-Slc37a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415075	M	MP:0001146	abnormal testis morphology	Slc37a2<em1(IMPC)Mbp>/Slc37a2<em1(IMPC)Mbp>	C57BL/6NCrl-Slc37a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415075	M	MP:0001304	cataract	Slc37a2<em1(IMPC)Mbp>/Slc37a2<em1(IMPC)Mbp>	C57BL/6NCrl-Slc37a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415075	F	MP:0000062	increased bone mineral density	Slc37a2<em1(IMPC)Mbp>/Slc37a2<em1(IMPC)Mbp>	C57BL/6NCrl-Slc37a2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415076	M	MP:0001304	cataract	Slfn14<em1(IMPC)Tcp>/Slfn14<em1(IMPC)Tcp>	C57BL/6NCrl-Slfn14<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415076	F	MP:0005561	increased mean corpuscular hemoglobin	Slfn14<em1(IMPC)Tcp>/Slfn14<em1(IMPC)Tcp>	C57BL/6NCrl-Slfn14<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415076	F	MP:0000470	abnormal stomach morphology	Slfn14<em1(IMPC)Tcp>/Slfn14<em1(IMPC)Tcp>	C57BL/6NCrl-Slfn14<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415076	M	MP:0001303	abnormal lens morphology	Slfn14<em1(IMPC)Tcp>/Slfn14<em1(IMPC)Tcp>	C57BL/6NCrl-Slfn14<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415076	M	MP:0010067	increased red blood cell distribution width	Slfn14<em1(IMPC)Tcp>/Slfn14<em1(IMPC)Tcp>	C57BL/6NCrl-Slfn14<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415077	F	MP:0002590	increased mean corpuscular volume	Slfn1<tm1.1(KOMP)Vlcg>/Slfn1<tm1.1(KOMP)Vlcg>	C57BL/6NCrl-Slfn1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7415077	F	MP:0010506	prolonged RR interval	Slfn1<tm1.1(KOMP)Vlcg>/Slfn1<tm1.1(KOMP)Vlcg>	C57BL/6NCrl-Slfn1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7415078	F	MP:0002966	decreased circulating alkaline phosphatase level	Smad3<em1(IMPC)H>/Smad3<+>	C57BL/6NTac-Smad3<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415079	M	MP:0002591	decreased mean corpuscular volume	Smarce1<em1(IMPC)J>/Smarce1<+>	C57BL/6NJ-Smarce1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415080	M	MP:0009142	decreased prepulse inhibition	Smchd1<em1(IMPC)Tcp>/Smchd1<+>	C57BL/6NCrl-Smchd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415080	M	MP:0000157	abnormal sternum morphology	Smchd1<em1(IMPC)Tcp>/Smchd1<+>	C57BL/6NCrl-Smchd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415081	M	MP:0000470	abnormal stomach morphology	Smchd1<em1(IMPC)Tcp>/Smchd1<em1(IMPC)Tcp>	C57BL/6NCrl-Smchd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415081	F	MP:0011100	preweaning lethality, complete penetrance	Smchd1<em1(IMPC)Tcp>/Smchd1<em1(IMPC)Tcp>	C57BL/6NCrl-Smchd1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415083	F	MP:0010053	decreased grip strength	Socs2<em1(IMPC)H>/Socs2<em1(IMPC)H>	C57BL/6NTac-Socs2<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415083	F	MP:0005553	increased circulating creatinine level	Socs2<em1(IMPC)H>/Socs2<em1(IMPC)H>	C57BL/6NTac-Socs2<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415084	F	MP:0001402	decreased locomotor activity	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0010124	decreased bone mineral content	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0002135	abnormal kidney morphology	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0000274	enlarged heart	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0000220	increased monocyte cell number	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	F	MP:0000598	abnormal liver morphology	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0002590	increased mean corpuscular volume	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	F	MP:0001399	hyperactivity	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0005179	decreased circulating cholesterol level	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0001489	decreased startle reflex	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	F	MP:0000601	small liver	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0000186	decreased circulating HDL cholesterol level	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0010025	decreased total body fat amount	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0003960	increased lean body mass	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0000063	decreased bone mineral density	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0005419	decreased circulating serum albumin level	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	F	MP:0001417	decreased exploration in new environment	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0003068	enlarged kidney	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415084	M	MP:0000266	abnormal heart morphology	Sox21<em1(IMPC)Mbp>/Sox21<em1(IMPC)Mbp>	C57BL/6NCrl-Sox21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415085	F	MP:0001325	abnormal retina morphology	Sox4<em1(IMPC)Mbp>/Sox4<+>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415085	F	MP:0009342	enlarged gallbladder	Sox4<em1(IMPC)Mbp>/Sox4<+>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415085	M	MP:0002152	abnormal brain morphology	Sox4<em1(IMPC)Mbp>/Sox4<+>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415085	M	MP:0000774	decreased brain size	Sox4<em1(IMPC)Mbp>/Sox4<+>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415085	F	MP:0001258	decreased body length	Sox4<em1(IMPC)Mbp>/Sox4<+>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415085	F	MP:0010097	abnormal retina blood vessel morphology	Sox4<em1(IMPC)Mbp>/Sox4<+>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415085	M	MP:0002792	abnormal retina vasculature morphology	Sox4<em1(IMPC)Mbp>/Sox4<+>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415085	F	MP:0001120	abnormal uterus morphology	Sox4<em1(IMPC)Mbp>/Sox4<+>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415085	F	MP:0004906	enlarged uterus	Sox4<em1(IMPC)Mbp>/Sox4<+>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415085	F	MP:0020421	increased freezing behavior	Sox4<em1(IMPC)Mbp>/Sox4<+>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415085	F	MP:0005084	abnormal gallbladder morphology	Sox4<em1(IMPC)Mbp>/Sox4<+>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415086	M	MP:0006108	abnormal hindbrain development	Sox4<em1(IMPC)Mbp>/Sox4<em1(IMPC)Mbp>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415086	M	MP:0002151	abnormal neural tube morphology	Sox4<em1(IMPC)Mbp>/Sox4<em1(IMPC)Mbp>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415086	M	MP:0003720	abnormal neural tube closure	Sox4<em1(IMPC)Mbp>/Sox4<em1(IMPC)Mbp>	C57BL/6NCrl-Sox4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415088	M	MP:0003068	enlarged kidney	Sptan1<em1(IMPC)Mbp>/Sptan1<+>	C57BL/6NCrl-Sptan1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415088	F	MP:0001289	persistence of hyaloid vascular system	Sptan1<em1(IMPC)Mbp>/Sptan1<+>	C57BL/6NCrl-Sptan1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415088	M	MP:0002135	abnormal kidney morphology	Sptan1<em1(IMPC)Mbp>/Sptan1<+>	C57BL/6NCrl-Sptan1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415088	F	MP:0001258	decreased body length	Sptan1<em1(IMPC)Mbp>/Sptan1<+>	C57BL/6NCrl-Sptan1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415088	M	MP:0001304	cataract	Sptan1<em1(IMPC)Mbp>/Sptan1<+>	C57BL/6NCrl-Sptan1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415088	F	MP:0002092	abnormal eye morphology	Sptan1<em1(IMPC)Mbp>/Sptan1<+>	C57BL/6NCrl-Sptan1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415088	M	MP:0002699	abnormal vitreous body morphology	Sptan1<em1(IMPC)Mbp>/Sptan1<+>	C57BL/6NCrl-Sptan1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415089	M	MP:0003232	abnormal forebrain development	Sptan1<em1(IMPC)Mbp>/Sptan1<em1(IMPC)Mbp>	C57BL/6NCrl-Sptan1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415089	M	MP:0003984	embryonic growth retardation	Sptan1<em1(IMPC)Mbp>/Sptan1<em1(IMPC)Mbp>	C57BL/6NCrl-Sptan1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415090	M	MP:0008259	abnormal optic disk morphology	Sptlc3<em1(IMPC)Hmgu>/Sptlc3<em1(IMPC)Hmgu>	C57BL/6NCrl-Sptlc3<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415090	M	MP:0001303	abnormal lens morphology	Sptlc3<em1(IMPC)Hmgu>/Sptlc3<em1(IMPC)Hmgu>	C57BL/6NCrl-Sptlc3<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415090	M	MP:0001304	cataract	Sptlc3<em1(IMPC)Hmgu>/Sptlc3<em1(IMPC)Hmgu>	C57BL/6NCrl-Sptlc3<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415090	M	MP:0000194	increased circulating calcium level	Sptlc3<em1(IMPC)Hmgu>/Sptlc3<em1(IMPC)Hmgu>	C57BL/6NCrl-Sptlc3<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415091	F	MP:0004924	abnormal behavior	Srp72<em1(IMPC)Bay>/Srp72<+>	C57BL/6N-Srp72<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415091	F	MP:0020870	decreased thigmotaxis	Srp72<em1(IMPC)Bay>/Srp72<+>	C57BL/6N-Srp72<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415091	F	MP:0001402	decreased locomotor activity	Srp72<em1(IMPC)Bay>/Srp72<+>	C57BL/6N-Srp72<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415091	F	MP:0002574	increased vertical activity	Srp72<em1(IMPC)Bay>/Srp72<+>	C57BL/6N-Srp72<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415093	F	MP:0000198	decreased circulating phosphate level	Srpx2<em1(IMPC)Hmgu>/Srpx2<em1(IMPC)Hmgu>	C57BL/6NCrl-Srpx2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415094	F	MP:0002092	abnormal eye morphology	Srr<em1(IMPC)Mbp>/Srr<em1(IMPC)Mbp>	C57BL/6NCrl-Srr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415094	M	MP:0000266	abnormal heart morphology	Srr<em1(IMPC)Mbp>/Srr<em1(IMPC)Mbp>	C57BL/6NCrl-Srr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415094	M	MP:0000274	enlarged heart	Srr<em1(IMPC)Mbp>/Srr<em1(IMPC)Mbp>	C57BL/6NCrl-Srr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415094	M	MP:0001147	small testis	Srr<em1(IMPC)Mbp>/Srr<em1(IMPC)Mbp>	C57BL/6NCrl-Srr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415094	M	MP:0001146	abnormal testis morphology	Srr<em1(IMPC)Mbp>/Srr<em1(IMPC)Mbp>	C57BL/6NCrl-Srr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415094	M	MP:0002060	abnormal skin morphology	Srr<em1(IMPC)Mbp>/Srr<em1(IMPC)Mbp>	C57BL/6NCrl-Srr<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415095	M	MP:0005559	increased circulating glucose level	Ss18<em1(IMPC)J>/Ss18<+>	C57BL/6NJ-Ss18<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415097	M	MP:0003271	abnormal duodenum morphology	Stpg4<em1(IMPC)Rbrc>/Stpg4<em1(IMPC)Rbrc>	C57BL/6NJcl-Stpg4<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415098	M	MP:0009908	protruding tongue	Strada<em1(IMPC)Bay>/Strada<em1(IMPC)Bay>	C57BL/6N-Strada<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415098	M	MP:0000111	cleft palate	Strada<em1(IMPC)Bay>/Strada<em1(IMPC)Bay>	C57BL/6N-Strada<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415099	M	MP:0010097	abnormal retina blood vessel morphology	Strn4<tm1b(EUCOMM)Hmgu>/Strn4<+>	C57BL/6NCrl-Strn4<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:7415099	F	MP:0001364	decreased anxiety-related response	Strn4<tm1b(EUCOMM)Hmgu>/Strn4<+>	C57BL/6NCrl-Strn4<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:7415099	F	MP:0004924	abnormal behavior	Strn4<tm1b(EUCOMM)Hmgu>/Strn4<+>	C57BL/6NCrl-Strn4<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:7415099	F	MP:0020870	decreased thigmotaxis	Strn4<tm1b(EUCOMM)Hmgu>/Strn4<+>	C57BL/6NCrl-Strn4<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:7415099	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Strn4<tm1b(EUCOMM)Hmgu>/Strn4<+>	C57BL/6NCrl-Strn4<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:7415099	M	MP:0005562	decreased mean corpuscular hemoglobin	Strn4<tm1b(EUCOMM)Hmgu>/Strn4<+>	C57BL/6NCrl-Strn4<tm1b(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:7415100	M	MP:0000706	small thymus	Stx7<em1(IMPC)Rbrc>/Stx7<em1(IMPC)Rbrc>	C57BL/6NJcl-Stx7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415100	M	MP:0000703	abnormal thymus morphology	Stx7<em1(IMPC)Rbrc>/Stx7<em1(IMPC)Rbrc>	C57BL/6NJcl-Stx7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415100	F	MP:0001565	abnormal circulating phosphate level	Stx7<em1(IMPC)Rbrc>/Stx7<em1(IMPC)Rbrc>	C57BL/6NJcl-Stx7<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415101	F	MP:0011110	preweaning lethality, incomplete penetrance	Svil<em1(IMPC)Bay>/Svil<em1(IMPC)Bay>	C57BL/6N-Svil<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415104	M	MP:0001785	edema	Szt2<em1(IMPC)Bay>/Szt2<em1(IMPC)Bay>	C57BL/6N-Szt2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415104	M	MP:0001914	hemorrhage	Szt2<em1(IMPC)Bay>/Szt2<em1(IMPC)Bay>	C57BL/6N-Szt2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415106	M	MP:0002092	abnormal eye morphology	Tbx1<em1(IMPC)Mbp>/Tbx1<+>	C57BL/6NCrl-Tbx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415106	M	MP:0001293	anophthalmia	Tbx1<em1(IMPC)Mbp>/Tbx1<+>	C57BL/6NCrl-Tbx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415106	F	MP:0001944	abnormal pancreas morphology	Tbx1<em1(IMPC)Mbp>/Tbx1<+>	C57BL/6NCrl-Tbx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415106	F	MP:0001297	microphthalmia	Tbx1<em1(IMPC)Mbp>/Tbx1<+>	C57BL/6NCrl-Tbx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415106	F	MP:0002060	abnormal skin morphology	Tbx1<em1(IMPC)Mbp>/Tbx1<+>	C57BL/6NCrl-Tbx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415106	F	MP:0001614	abnormal blood vessel morphology	Tbx1<em1(IMPC)Mbp>/Tbx1<+>	C57BL/6NCrl-Tbx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415106	F	MP:0001399	hyperactivity	Tbx1<em1(IMPC)Mbp>/Tbx1<+>	C57BL/6NCrl-Tbx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415106	F	MP:0001711	abnormal placenta morphology	Tbx1<em1(IMPC)Mbp>/Tbx1<+>	C57BL/6NCrl-Tbx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415107	M	MP:0003984	embryonic growth retardation	Tbx1<em1(IMPC)Mbp>/Tbx1<em1(IMPC)Mbp>	C57BL/6NCrl-Tbx1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415108	F	MP:0002792	abnormal retina vasculature morphology	Tbx3<em1(IMPC)Mbp>/Tbx3<+>	C57BL/6NCrl-Tbx3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415108	F	MP:0002339	abnormal lymph node morphology	Tbx3<em1(IMPC)Mbp>/Tbx3<+>	C57BL/6NCrl-Tbx3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415108	F	MP:0002092	abnormal eye morphology	Tbx3<em1(IMPC)Mbp>/Tbx3<+>	C57BL/6NCrl-Tbx3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415108	F	MP:0001297	microphthalmia	Tbx3<em1(IMPC)Mbp>/Tbx3<+>	C57BL/6NCrl-Tbx3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415108	F	MP:0006203	eye hemorrhage	Tbx3<em1(IMPC)Mbp>/Tbx3<+>	C57BL/6NCrl-Tbx3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415108	M	MP:0001402	decreased locomotor activity	Tbx3<em1(IMPC)Mbp>/Tbx3<+>	C57BL/6NCrl-Tbx3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415108	M	MP:0000691	enlarged spleen	Tbx3<em1(IMPC)Mbp>/Tbx3<+>	C57BL/6NCrl-Tbx3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415108	M	MP:0000689	abnormal spleen morphology	Tbx3<em1(IMPC)Mbp>/Tbx3<+>	C57BL/6NCrl-Tbx3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415111	M	MP:0000702	enlarged lymph nodes	Tdp1<em1(IMPC)Tcp>/Tdp1<em1(IMPC)Tcp>	C57BL/6NCrl-Tdp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415111	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Tdp1<em1(IMPC)Tcp>/Tdp1<em1(IMPC)Tcp>	C57BL/6NCrl-Tdp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415111	F	MP:0001417	decreased exploration in new environment	Tdp1<em1(IMPC)Tcp>/Tdp1<em1(IMPC)Tcp>	C57BL/6NCrl-Tdp1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415112	M	MP:0001944	abnormal pancreas morphology	Tecr<em1(IMPC)Rbrc>/Tecr<+>	C57BL/6NJcl-Tecr<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415112	M	MP:0000182	increased circulating LDL cholesterol level	Tecr<em1(IMPC)Rbrc>/Tecr<+>	C57BL/6NJcl-Tecr<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415114	M	MP:0002941	increased circulating alanine transaminase level	Tenm1<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Tenm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415114	M	MP:0005562	decreased mean corpuscular hemoglobin	Tenm1<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Tenm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415114	M	MP:0001417	decreased exploration in new environment	Tenm1<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Tenm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415114	M	MP:0002591	decreased mean corpuscular volume	Tenm1<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Tenm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415115	F	MP:0000208	decreased hematocrit	Tenm1<em1(IMPC)Tcp>/Tenm1<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415115	F	MP:0002591	decreased mean corpuscular volume	Tenm1<em1(IMPC)Tcp>/Tenm1<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415115	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Tenm1<em1(IMPC)Tcp>/Tenm1<em1(IMPC)Tcp>	C57BL/6NCrl-Tenm1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415116	F	MP:0000274	enlarged heart	Tgfbr2<em1(IMPC)Rbrc>/Tgfbr2<+>	C57BL/6NJcl-Tgfbr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415116	F	MP:0000598	abnormal liver morphology	Tgfbr2<em1(IMPC)Rbrc>/Tgfbr2<+>	C57BL/6NJcl-Tgfbr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415116	F	MP:0002135	abnormal kidney morphology	Tgfbr2<em1(IMPC)Rbrc>/Tgfbr2<+>	C57BL/6NJcl-Tgfbr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415116	F	MP:0003068	enlarged kidney	Tgfbr2<em1(IMPC)Rbrc>/Tgfbr2<+>	C57BL/6NJcl-Tgfbr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415116	F	MP:0000601	small liver	Tgfbr2<em1(IMPC)Rbrc>/Tgfbr2<+>	C57BL/6NJcl-Tgfbr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415116	F	MP:0000266	abnormal heart morphology	Tgfbr2<em1(IMPC)Rbrc>/Tgfbr2<+>	C57BL/6NJcl-Tgfbr2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415118	M	MP:0004958	enlarged prostate gland	Thbs2<em1(IMPC)Mbp>/Thbs2<em1(IMPC)Mbp>	C57BL/6NCrl-Thbs2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415118	F	MP:0000691	enlarged spleen	Thbs2<em1(IMPC)Mbp>/Thbs2<em1(IMPC)Mbp>	C57BL/6NCrl-Thbs2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415118	F	MP:0002989	small kidney	Thbs2<em1(IMPC)Mbp>/Thbs2<em1(IMPC)Mbp>	C57BL/6NCrl-Thbs2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415118	F	MP:0002135	abnormal kidney morphology	Thbs2<em1(IMPC)Mbp>/Thbs2<em1(IMPC)Mbp>	C57BL/6NCrl-Thbs2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415118	M	MP:0001304	cataract	Thbs2<em1(IMPC)Mbp>/Thbs2<em1(IMPC)Mbp>	C57BL/6NCrl-Thbs2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415118	M	MP:0001158	abnormal prostate gland morphology	Thbs2<em1(IMPC)Mbp>/Thbs2<em1(IMPC)Mbp>	C57BL/6NCrl-Thbs2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415118	F	MP:0000689	abnormal spleen morphology	Thbs2<em1(IMPC)Mbp>/Thbs2<em1(IMPC)Mbp>	C57BL/6NCrl-Thbs2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415119	F	MP:0003961	decreased lean body mass	Thoc1<em1(IMPC)Ccpcz>/Thoc1<+>	C57BL/6NCrl-Thoc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415119	F	MP:0000709	enlarged thymus	Thoc1<em1(IMPC)Ccpcz>/Thoc1<+>	C57BL/6NCrl-Thoc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415119	F	MP:0005561	increased mean corpuscular hemoglobin	Thoc1<em1(IMPC)Ccpcz>/Thoc1<+>	C57BL/6NCrl-Thoc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415119	M	MP:0000266	abnormal heart morphology	Thoc1<em1(IMPC)Ccpcz>/Thoc1<+>	C57BL/6NCrl-Thoc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415119	F	MP:0000703	abnormal thymus morphology	Thoc1<em1(IMPC)Ccpcz>/Thoc1<+>	C57BL/6NCrl-Thoc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415119	M	MP:0000274	enlarged heart	Thoc1<em1(IMPC)Ccpcz>/Thoc1<+>	C57BL/6NCrl-Thoc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415119	M	MP:0002135	abnormal kidney morphology	Thoc1<em1(IMPC)Ccpcz>/Thoc1<+>	C57BL/6NCrl-Thoc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415119	F	MP:0010024	increased total body fat amount	Thoc1<em1(IMPC)Ccpcz>/Thoc1<+>	C57BL/6NCrl-Thoc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415119	F	MP:0002590	increased mean corpuscular volume	Thoc1<em1(IMPC)Ccpcz>/Thoc1<+>	C57BL/6NCrl-Thoc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415119	M	MP:0003917	increased kidney weight	Thoc1<em1(IMPC)Ccpcz>/Thoc1<+>	C57BL/6NCrl-Thoc1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415121	F	MP:0002092	abnormal eye morphology	Thop1<em1(IMPC)Mbp>/Thop1<em1(IMPC)Mbp>	C57BL/6NCrl-Thop1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415121	M	MP:0002997	enlarged seminal vesicle	Thop1<em1(IMPC)Mbp>/Thop1<em1(IMPC)Mbp>	C57BL/6NCrl-Thop1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415121	F	MP:0000221	decreased leukocyte cell number	Thop1<em1(IMPC)Mbp>/Thop1<em1(IMPC)Mbp>	C57BL/6NCrl-Thop1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415121	M	MP:0001146	abnormal testis morphology	Thop1<em1(IMPC)Mbp>/Thop1<em1(IMPC)Mbp>	C57BL/6NCrl-Thop1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415121	F	MP:0000691	enlarged spleen	Thop1<em1(IMPC)Mbp>/Thop1<em1(IMPC)Mbp>	C57BL/6NCrl-Thop1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415121	F	MP:0002135	abnormal kidney morphology	Thop1<em1(IMPC)Mbp>/Thop1<em1(IMPC)Mbp>	C57BL/6NCrl-Thop1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415121	F	MP:0002060	abnormal skin morphology	Thop1<em1(IMPC)Mbp>/Thop1<em1(IMPC)Mbp>	C57BL/6NCrl-Thop1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415121	F	MP:0000689	abnormal spleen morphology	Thop1<em1(IMPC)Mbp>/Thop1<em1(IMPC)Mbp>	C57BL/6NCrl-Thop1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415121	F	MP:0002989	small kidney	Thop1<em1(IMPC)Mbp>/Thop1<em1(IMPC)Mbp>	C57BL/6NCrl-Thop1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415121	M	MP:0001289	persistence of hyaloid vascular system	Thop1<em1(IMPC)Mbp>/Thop1<em1(IMPC)Mbp>	C57BL/6NCrl-Thop1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415123	M	MP:0000598	abnormal liver morphology	Tmed6<em1(IMPC)Rbrc>/Tmed6<em1(IMPC)Rbrc>	C57BL/6NJcl-Tmed6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415123	M	MP:0001944	abnormal pancreas morphology	Tmed6<em1(IMPC)Rbrc>/Tmed6<em1(IMPC)Rbrc>	C57BL/6NJcl-Tmed6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415123	M	MP:0004247	small pancreas	Tmed6<em1(IMPC)Rbrc>/Tmed6<em1(IMPC)Rbrc>	C57BL/6NJcl-Tmed6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415123	F	MP:0001417	decreased exploration in new environment	Tmed6<em1(IMPC)Rbrc>/Tmed6<em1(IMPC)Rbrc>	C57BL/6NJcl-Tmed6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415123	M	MP:0000599	enlarged liver	Tmed6<em1(IMPC)Rbrc>/Tmed6<em1(IMPC)Rbrc>	C57BL/6NJcl-Tmed6<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415124	M	MP:0005632	decreased circulating aspartate transaminase level	Tmem212<em1(IMPC)J>/Tmem212<em1(IMPC)J>	C57BL/6NJ-Tmem212<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415124	F	MP:0005278	abnormal cholesterol homeostasis	Tmem212<em1(IMPC)J>/Tmem212<em1(IMPC)J>	C57BL/6NJ-Tmem212<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415124	M	MP:0003131	increased erythrocyte cell number	Tmem212<em1(IMPC)J>/Tmem212<em1(IMPC)J>	C57BL/6NJ-Tmem212<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415125	M	MP:0001891	hydrocephaly	Tmem63c<em1(IMPC)Rbrc>/Tmem63c<em1(IMPC)Rbrc>	C57BL/6NJcl-Tmem63c<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415125	M	MP:0010024	increased total body fat amount	Tmem63c<em1(IMPC)Rbrc>/Tmem63c<em1(IMPC)Rbrc>	C57BL/6NJcl-Tmem63c<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415125	M	MP:0002152	abnormal brain morphology	Tmem63c<em1(IMPC)Rbrc>/Tmem63c<em1(IMPC)Rbrc>	C57BL/6NJcl-Tmem63c<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415127	F	MP:0003313	abnormal locomotor activation	Tnr<em1(IMPC)Rbrc>/Tnr<em1(IMPC)Rbrc>	C57BL/6NJcl-Tnr<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415127	F	MP:0004952	increased spleen weight	Tnr<em1(IMPC)Rbrc>/Tnr<em1(IMPC)Rbrc>	C57BL/6NJcl-Tnr<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415128	M	MP:0002092	abnormal eye morphology	Top2b<em1(IMPC)Mbp>/Top2b<+>	C57BL/6NCrl-Top2b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415129	F	MP:0011495	abnormal head shape	Top2b<em1(IMPC)Mbp>/Top2b<em1(IMPC)Mbp>	C57BL/6NCrl-Top2b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415129	F	MP:0001711	abnormal placenta morphology	Top2b<em1(IMPC)Mbp>/Top2b<em1(IMPC)Mbp>	C57BL/6NCrl-Top2b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415130	M	MP:0005419	decreased circulating serum albumin level	Topors<em1(IMPC)J>/Topors<em1(IMPC)J>	C57BL/6NJ-Topors<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415130	M	MP:0002834	decreased heart weight	Topors<em1(IMPC)J>/Topors<em1(IMPC)J>	C57BL/6NJ-Topors<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415130	M	MP:0000208	decreased hematocrit	Topors<em1(IMPC)J>/Topors<em1(IMPC)J>	C57BL/6NJ-Topors<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415130	M	MP:0005559	increased circulating glucose level	Topors<em1(IMPC)J>/Topors<em1(IMPC)J>	C57BL/6NJ-Topors<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415130	M	MP:0002968	increased circulating alkaline phosphatase level	Topors<em1(IMPC)J>/Topors<em1(IMPC)J>	C57BL/6NJ-Topors<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415130	M	MP:0005567	decreased circulating total protein level	Topors<em1(IMPC)J>/Topors<em1(IMPC)J>	C57BL/6NJ-Topors<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415130	M	MP:0002875	decreased erythrocyte cell number	Topors<em1(IMPC)J>/Topors<em1(IMPC)J>	C57BL/6NJ-Topors<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415130	F	MP:0005333	decreased heart rate	Topors<em1(IMPC)J>/Topors<em1(IMPC)J>	C57BL/6NJ-Topors<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415130	F	MP:0001926	female infertility	Topors<em1(IMPC)J>/Topors<em1(IMPC)J>	C57BL/6NJ-Topors<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415130	F	MP:0003961	decreased lean body mass	Topors<em1(IMPC)J>/Topors<em1(IMPC)J>	C57BL/6NJ-Topors<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415130	F	MP:0002574	increased vertical activity	Topors<em1(IMPC)J>/Topors<em1(IMPC)J>	C57BL/6NJ-Topors<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415130	F	MP:0010124	decreased bone mineral content	Topors<em1(IMPC)J>/Topors<em1(IMPC)J>	C57BL/6NJ-Topors<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415130	F	MP:0010024	increased total body fat amount	Topors<em1(IMPC)J>/Topors<em1(IMPC)J>	C57BL/6NJ-Topors<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415131	M	MP:0000702	enlarged lymph nodes	Traf7<em1(IMPC)Tcp>/Traf7<+>	C57BL/6NCrl-Traf7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415131	F	MP:0001303	abnormal lens morphology	Traf7<em1(IMPC)Tcp>/Traf7<+>	C57BL/6NCrl-Traf7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415131	F	MP:0001304	cataract	Traf7<em1(IMPC)Tcp>/Traf7<+>	C57BL/6NCrl-Traf7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415135	F	MP:0005293	impaired glucose tolerance	Trio<em1(IMPC)H>/Trio<+>	C57BL/6NTac-Trio<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415137	F	MP:0010097	abnormal retina blood vessel morphology	Tspan8<em1(IMPC)Hmgu>/Tspan8<em1(IMPC)Hmgu>	C57BL/6NCrl-Tspan8<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415137	F	MP:0001289	persistence of hyaloid vascular system	Tspan8<em1(IMPC)Hmgu>/Tspan8<em1(IMPC)Hmgu>	C57BL/6NCrl-Tspan8<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415139	F	MP:0002591	decreased mean corpuscular volume	Ttyh3<em1(IMPC)Tcp>/Ttyh3<em1(IMPC)Tcp>	C57BL/6NCrl-Ttyh3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415139	F	MP:0005641	increased mean corpuscular hemoglobin concentration	Ttyh3<em1(IMPC)Tcp>/Ttyh3<em1(IMPC)Tcp>	C57BL/6NCrl-Ttyh3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415140	M	MP:0003960	increased lean body mass	Twist1<em1(IMPC)Rbrc>/Twist1<+>	C57BL/6NJcl-Twist1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415140	M	MP:0010025	decreased total body fat amount	Twist1<em1(IMPC)Rbrc>/Twist1<+>	C57BL/6NJcl-Twist1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415140	F	MP:0010052	increased grip strength	Twist1<em1(IMPC)Rbrc>/Twist1<+>	C57BL/6NJcl-Twist1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415140	M	MP:0009142	decreased prepulse inhibition	Twist1<em1(IMPC)Rbrc>/Twist1<+>	C57BL/6NJcl-Twist1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415141	M	MP:0001289	persistence of hyaloid vascular system	Txnl1<em1(IMPC)Tcp>/Txnl1<em1(IMPC)Tcp>	C57BL/6NCrl-Txnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415141	M	MP:0005562	decreased mean corpuscular hemoglobin	Txnl1<em1(IMPC)Tcp>/Txnl1<em1(IMPC)Tcp>	C57BL/6NCrl-Txnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415141	F	MP:0000208	decreased hematocrit	Txnl1<em1(IMPC)Tcp>/Txnl1<em1(IMPC)Tcp>	C57BL/6NCrl-Txnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415141	M	MP:0000220	increased monocyte cell number	Txnl1<em1(IMPC)Tcp>/Txnl1<em1(IMPC)Tcp>	C57BL/6NCrl-Txnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415141	F	MP:0010123	increased bone mineral content	Txnl1<em1(IMPC)Tcp>/Txnl1<em1(IMPC)Tcp>	C57BL/6NCrl-Txnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415141	M	MP:0003131	increased erythrocyte cell number	Txnl1<em1(IMPC)Tcp>/Txnl1<em1(IMPC)Tcp>	C57BL/6NCrl-Txnl1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415142	M	MP:0001146	abnormal testis morphology	Tyro3<em1(IMPC)Ccpcz>/Tyro3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tyro3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415142	M	MP:0002092	abnormal eye morphology	Tyro3<em1(IMPC)Ccpcz>/Tyro3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tyro3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415142	F	MP:0000709	enlarged thymus	Tyro3<em1(IMPC)Ccpcz>/Tyro3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tyro3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415142	M	MP:0000266	abnormal heart morphology	Tyro3<em1(IMPC)Ccpcz>/Tyro3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tyro3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415142	M	MP:0004083	polysyndactyly	Tyro3<em1(IMPC)Ccpcz>/Tyro3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tyro3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415142	M	MP:0002339	abnormal lymph node morphology	Tyro3<em1(IMPC)Ccpcz>/Tyro3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tyro3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415142	M	MP:0002100	abnormal tooth morphology	Tyro3<em1(IMPC)Ccpcz>/Tyro3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tyro3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415142	F	MP:0001175	abnormal lung morphology	Tyro3<em1(IMPC)Ccpcz>/Tyro3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tyro3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415142	M	MP:0000274	enlarged heart	Tyro3<em1(IMPC)Ccpcz>/Tyro3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tyro3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415142	M	MP:0001147	small testis	Tyro3<em1(IMPC)Ccpcz>/Tyro3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tyro3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415142	M	MP:0005011	increased eosinophil cell number	Tyro3<em1(IMPC)Ccpcz>/Tyro3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tyro3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415142	F	MP:0000703	abnormal thymus morphology	Tyro3<em1(IMPC)Ccpcz>/Tyro3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tyro3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415142	M	MP:0002060	abnormal skin morphology	Tyro3<em1(IMPC)Ccpcz>/Tyro3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tyro3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415145	F	MP:0005265	abnormal blood urea nitrogen level	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	M	MP:0002590	increased mean corpuscular volume	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	M	MP:0004930	small epididymis	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	M	MP:0001147	small testis	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	M	MP:0002631	abnormal epididymis morphology	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	M	MP:0005016	decreased lymphocyte cell number	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	F	MP:0001399	hyperactivity	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	F	MP:0001258	decreased body length	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	F	MP:0001926	female infertility	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	F	MP:0000226	abnormal mean corpuscular volume	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	M	MP:0001146	abnormal testis morphology	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	M	MP:0000221	decreased leukocyte cell number	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	F	MP:0000063	decreased bone mineral density	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	F	MP:0005011	increased eosinophil cell number	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	M	MP:0001925	male infertility	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	F	MP:0003795	abnormal bone structure	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415145	F	MP:0000598	abnormal liver morphology	Ube2j2<em1(IMPC)Rbrc>/Ube2j2<em1(IMPC)Rbrc>	C57BL/6NJcl-Ube2j2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415146	F	MP:0003921	abnormal heart left ventricle morphology	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6NCrl-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:7415146	F	MP:0005599	increased cardiac muscle contractility	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6NCrl-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:7415146	F	MP:0002968	increased circulating alkaline phosphatase level	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6NCrl-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:7415146	M	MP:0001402	decreased locomotor activity	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6NCrl-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:7415146	F	MP:0013510	decreased CD4-negative NK T cell number	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6NCrl-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:7415146	F	MP:0004151	decreased circulating iron level	Ube3c<tm1b(EUCOMM)Hmgu>/Ube3c<tm1b(EUCOMM)Hmgu>	C57BL/6NCrl-Ube3c<tm1b(EUCOMM)Hmgu>/Rbrc	N	MGI:5576271
MGI:7415147	M	MP:0001147	small testis	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	F	MP:0001258	decreased body length	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	F	MP:0005343	increased circulating aspartate transaminase level	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	M	MP:0020420	abnormal freezing behavior	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	F	MP:0000598	abnormal liver morphology	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	M	MP:0009453	enhanced contextual conditioning behavior	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	M	MP:0001146	abnormal testis morphology	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	M	MP:0009455	enhanced cued conditioning behavior	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	F	MP:0001417	decreased exploration in new environment	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	F	MP:0000691	enlarged spleen	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	F	MP:0002968	increased circulating alkaline phosphatase level	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	M	MP:0020421	increased freezing behavior	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	F	MP:0000689	abnormal spleen morphology	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	F	MP:0000601	small liver	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415147	F	MP:0000692	small spleen	Ubqln4<em1(IMPC)Mbp>/Ubqln4<em1(IMPC)Mbp>	C57BL/6NCrl-Ubqln4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415148	M	MP:0000219	increased neutrophil cell number	Ugcg<em1(IMPC)H>/Ugcg<+>	C57BL/6NTac-Ugcg<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415148	M	MP:0005016	decreased lymphocyte cell number	Ugcg<em1(IMPC)H>/Ugcg<+>	C57BL/6NTac-Ugcg<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415148	F	MP:0002941	increased circulating alanine transaminase level	Ugcg<em1(IMPC)H>/Ugcg<+>	C57BL/6NTac-Ugcg<em1(IMPC)H>/H	N	MGI:5576271
MGI:7415153	F	MP:0000709	enlarged thymus	Vegfd<em1(IMPC)Ccpcz>/Vegfd<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vegfd<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415153	F	MP:0000703	abnormal thymus morphology	Vegfd<em1(IMPC)Ccpcz>/Vegfd<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vegfd<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415153	M	MP:0000274	enlarged heart	Vegfd<em1(IMPC)Ccpcz>/Vegfd<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vegfd<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415153	M	MP:0000266	abnormal heart morphology	Vegfd<em1(IMPC)Ccpcz>/Vegfd<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vegfd<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415155	F	MP:0010067	increased red blood cell distribution width	Vps13c<tm1b(EUCOMM)Hmgu>/Vps13c<tm1b(EUCOMM)Hmgu>	C57BL/6NTac-Vps13c<tm1b(EUCOMM)Hmgu>/Ieg	N	MGI:5576271
MGI:7415158	F	MP:0000367	abnormal coat/ hair morphology	Vps37a<em1(IMPC)Tcp>/Vps37a<+>	C57BL/6NCrl-Vps37a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415158	F	MP:0001258	decreased body length	Vps37a<em1(IMPC)Tcp>/Vps37a<+>	C57BL/6NCrl-Vps37a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415158	F	MP:0020421	increased freezing behavior	Vps37a<em1(IMPC)Tcp>/Vps37a<+>	C57BL/6NCrl-Vps37a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415159	F	MP:0001697	abnormal embryo size	Vps37a<em1(IMPC)Tcp>/Vps37a<em1(IMPC)Tcp>	C57BL/6NCrl-Vps37a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415160	F	MP:0010123	increased bone mineral content	Vwce<em1(IMPC)Bay>/Vwce<em1(IMPC)Bay>	C57BL/6N-Vwce<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415160	F	MP:0011110	preweaning lethality, incomplete penetrance	Vwce<em1(IMPC)Bay>/Vwce<em1(IMPC)Bay>	C57BL/6N-Vwce<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415160	F	MP:0003795	abnormal bone structure	Vwce<em1(IMPC)Bay>/Vwce<em1(IMPC)Bay>	C57BL/6N-Vwce<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415163	M	MP:0005343	increased circulating aspartate transaminase level	Wdhd1<em1(IMPC)Rbrc>/Wdhd1<+>	C57BL/6NJcl-Wdhd1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415163	F	MP:0000681	abnormal thyroid gland morphology	Wdhd1<em1(IMPC)Rbrc>/Wdhd1<+>	C57BL/6NJcl-Wdhd1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415163	M	MP:0003917	increased kidney weight	Wdhd1<em1(IMPC)Rbrc>/Wdhd1<+>	C57BL/6NJcl-Wdhd1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415163	M	MP:0000274	enlarged heart	Wdhd1<em1(IMPC)Rbrc>/Wdhd1<+>	C57BL/6NJcl-Wdhd1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415163	M	MP:0000266	abnormal heart morphology	Wdhd1<em1(IMPC)Rbrc>/Wdhd1<+>	C57BL/6NJcl-Wdhd1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415163	F	MP:0005355	enlarged thyroid gland	Wdhd1<em1(IMPC)Rbrc>/Wdhd1<+>	C57BL/6NJcl-Wdhd1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415165	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Wdr33<em1(IMPC)Tcp>/Wdr33<+>	C57BL/6NCrl-Wdr33<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415165	M	MP:0009142	decreased prepulse inhibition	Wdr33<em1(IMPC)Tcp>/Wdr33<+>	C57BL/6NCrl-Wdr33<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415167	F	MP:0000601	small liver	Wipi1<em1(IMPC)Mbp>/Wipi1<em1(IMPC)Mbp>	C57BL/6NCrl-Wipi1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415167	F	MP:0000598	abnormal liver morphology	Wipi1<em1(IMPC)Mbp>/Wipi1<em1(IMPC)Mbp>	C57BL/6NCrl-Wipi1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415167	F	MP:0002135	abnormal kidney morphology	Wipi1<em1(IMPC)Mbp>/Wipi1<em1(IMPC)Mbp>	C57BL/6NCrl-Wipi1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415167	F	MP:0002989	small kidney	Wipi1<em1(IMPC)Mbp>/Wipi1<em1(IMPC)Mbp>	C57BL/6NCrl-Wipi1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415167	F	MP:0000691	enlarged spleen	Wipi1<em1(IMPC)Mbp>/Wipi1<em1(IMPC)Mbp>	C57BL/6NCrl-Wipi1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415167	F	MP:0000689	abnormal spleen morphology	Wipi1<em1(IMPC)Mbp>/Wipi1<em1(IMPC)Mbp>	C57BL/6NCrl-Wipi1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415168	M	MP:0001297	microphthalmia	Xpo4<em1(IMPC)Tcp>/Xpo4<+>	C57BL/6NCrl-Xpo4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415168	F	MP:0001325	abnormal retina morphology	Xpo4<em1(IMPC)Tcp>/Xpo4<+>	C57BL/6NCrl-Xpo4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7415170	M	MP:0003068	enlarged kidney	Ybx3<em1(IMPC)Rbrc>/Ybx3<em1(IMPC)Rbrc>	C57BL/6NJcl-Ybx3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415170	M	MP:0002135	abnormal kidney morphology	Ybx3<em1(IMPC)Rbrc>/Ybx3<em1(IMPC)Rbrc>	C57BL/6NJcl-Ybx3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415171	M	MP:0000689	abnormal spleen morphology	Zbtb16<em1(IMPC)Mbp>/Zbtb16<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415171	M	MP:0008259	abnormal optic disk morphology	Zbtb16<em1(IMPC)Mbp>/Zbtb16<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415171	F	MP:0001399	hyperactivity	Zbtb16<em1(IMPC)Mbp>/Zbtb16<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415171	M	MP:0001147	small testis	Zbtb16<em1(IMPC)Mbp>/Zbtb16<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415171	F	MP:0000274	enlarged heart	Zbtb16<em1(IMPC)Mbp>/Zbtb16<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415171	M	MP:0010025	decreased total body fat amount	Zbtb16<em1(IMPC)Mbp>/Zbtb16<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415171	M	MP:0003960	increased lean body mass	Zbtb16<em1(IMPC)Mbp>/Zbtb16<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415171	F	MP:0000266	abnormal heart morphology	Zbtb16<em1(IMPC)Mbp>/Zbtb16<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415171	M	MP:0009142	decreased prepulse inhibition	Zbtb16<em1(IMPC)Mbp>/Zbtb16<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415171	M	MP:0001146	abnormal testis morphology	Zbtb16<em1(IMPC)Mbp>/Zbtb16<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415171	M	MP:0000556	abnormal hindlimb morphology	Zbtb16<em1(IMPC)Mbp>/Zbtb16<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415171	M	MP:0000692	small spleen	Zbtb16<em1(IMPC)Mbp>/Zbtb16<em1(IMPC)Mbp>	C57BL/6NCrl-Zbtb16<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415172	M	MP:0002599	increased mean platelet volume	Zcchc17<em1(IMPC)Hmgu>/Zcchc17<em1(IMPC)Hmgu>	C57BL/6NCrl-Zcchc17<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415172	M	MP:0004952	increased spleen weight	Zcchc17<em1(IMPC)Hmgu>/Zcchc17<em1(IMPC)Hmgu>	C57BL/6NCrl-Zcchc17<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415172	F	MP:0002098	abnormal vibrissa morphology	Zcchc17<em1(IMPC)Hmgu>/Zcchc17<em1(IMPC)Hmgu>	C57BL/6NCrl-Zcchc17<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7415173	F	MP:0002092	abnormal eye morphology	Zdhhc14<em1(IMPC)Mbp>/Zdhhc14<em1(IMPC)Mbp>	C57BL/6NCrl-Zdhhc14<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415173	M	MP:0001146	abnormal testis morphology	Zdhhc14<em1(IMPC)Mbp>/Zdhhc14<em1(IMPC)Mbp>	C57BL/6NCrl-Zdhhc14<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415173	M	MP:0001147	small testis	Zdhhc14<em1(IMPC)Mbp>/Zdhhc14<em1(IMPC)Mbp>	C57BL/6NCrl-Zdhhc14<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415174	M	MP:0000274	enlarged heart	Zfat<em1(IMPC)Ccpcz>/Zfat<+>	C57BL/6NCrl-Zfat<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415174	M	MP:0000691	enlarged spleen	Zfat<em1(IMPC)Ccpcz>/Zfat<+>	C57BL/6NCrl-Zfat<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415174	M	MP:0000266	abnormal heart morphology	Zfat<em1(IMPC)Ccpcz>/Zfat<+>	C57BL/6NCrl-Zfat<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415174	M	MP:0000689	abnormal spleen morphology	Zfat<em1(IMPC)Ccpcz>/Zfat<+>	C57BL/6NCrl-Zfat<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7415176	M	MP:0001364	decreased anxiety-related response	Zfhx2<em1(IMPC)Rbrc>/Zfhx2<em1(IMPC)Rbrc>	C57BL/6NJcl-Zfhx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415176	M	MP:0001399	hyperactivity	Zfhx2<em1(IMPC)Rbrc>/Zfhx2<em1(IMPC)Rbrc>	C57BL/6NJcl-Zfhx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415176	M	MP:0002631	abnormal epididymis morphology	Zfhx2<em1(IMPC)Rbrc>/Zfhx2<em1(IMPC)Rbrc>	C57BL/6NJcl-Zfhx2<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7415177	F	MP:0000691	enlarged spleen	Zfp354a<em1(IMPC)Mbp>/Zfp354a<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp354a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415177	F	MP:0002339	abnormal lymph node morphology	Zfp354a<em1(IMPC)Mbp>/Zfp354a<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp354a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415177	F	MP:0000689	abnormal spleen morphology	Zfp354a<em1(IMPC)Mbp>/Zfp354a<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp354a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415177	F	MP:0002135	abnormal kidney morphology	Zfp354a<em1(IMPC)Mbp>/Zfp354a<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp354a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415177	F	MP:0000702	enlarged lymph nodes	Zfp354a<em1(IMPC)Mbp>/Zfp354a<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp354a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415177	F	MP:0005553	increased circulating creatinine level	Zfp354a<em1(IMPC)Mbp>/Zfp354a<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp354a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415177	F	MP:0000274	enlarged heart	Zfp354a<em1(IMPC)Mbp>/Zfp354a<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp354a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415177	F	MP:0000266	abnormal heart morphology	Zfp354a<em1(IMPC)Mbp>/Zfp354a<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp354a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415177	F	MP:0003068	enlarged kidney	Zfp354a<em1(IMPC)Mbp>/Zfp354a<em1(IMPC)Mbp>	C57BL/6NCrl-Zfp354a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7415178	M	MP:0010052	increased grip strength	Zfp74<em1(IMPC)J>/Zfp74<em1(IMPC)J>	C57BL/6NJ-Zfp74<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415179	F	MP:0009142	decreased prepulse inhibition	Zmym2<em1(IMPC)Bay>/Zmym2<+>	C57BL/6N-Zmym2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415179	M	MP:0001402	decreased locomotor activity	Zmym2<em1(IMPC)Bay>/Zmym2<+>	C57BL/6N-Zmym2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7415181	F	MP:0002968	increased circulating alkaline phosphatase level	Zmym2<em1(IMPC)J>/Zmym2<+>	C57BL/6NJ-Zmym2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415181	M	MP:0000218	increased leukocyte cell number	Zmym2<em1(IMPC)J>/Zmym2<+>	C57BL/6NJ-Zmym2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415181	M	MP:0010024	increased total body fat amount	Zmym2<em1(IMPC)J>/Zmym2<+>	C57BL/6NJ-Zmym2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415182	M	MP:0001700	abnormal embryo turning	Zmym2<em1(IMPC)J>/Zmym2<em1(IMPC)J>	C57BL/6NJ-Zmym2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7415182	M	MP:0003984	embryonic growth retardation	Zmym2<em1(IMPC)J>/Zmym2<em1(IMPC)J>	C57BL/6NJ-Zmym2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7423602	F	MP:0014443	impaired polar body extrusion	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	M	MP:0031269	increased susceptibility to diet-induced hepatic steatosis	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	M	MP:0002981	increased liver weight	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	M	MP:0008058	abnormal DNA repair	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	M	MP:0004499	increased incidence of tumors by chemical induction	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	M	MP:0010308	decreased tumor latency	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	F	MP:0010767	abnormal female meiosis I arrest	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	M	MP:0005165	increased susceptibility to injury	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	F	MP:0009661	abnormal pregnancy	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	F	MP:0001935	decreased litter size	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	M	MP:0005455	increased susceptibility to weight gain	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	F	MP:0001923	reduced female fertility	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	F	MP:0005389	reproductive system phenotype	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	Y	36240068
MGI:7423602	M	MP:0005516	enhanced liver regeneration	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	M	MP:0031271	increased susceptibility to age-related hepatic steatosis	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	F	MP:0008976	delayed female fertility	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7423602	M	MP:0003893	increased hepatocyte proliferation	Clspn<tm1(KOMP)Vlcg>/Clspn<+>	C57BL/6N-Clspn<tm1(KOMP)Vlcg>	N	36240068
MGI:7425189	M	MP:0008543	atrial fibrillation	Del(3)1Jfm/Del(3)1Jfm	involves: FVB	N	31636200
MGI:7425250	M	MP:0001783	decreased white adipose tissue amount	Adgra1<tm1.1Zgwg>/Adgra1<tm1.1Zgwg>	Not Specified	N	33824276
MGI:7425250	M	MP:0001780	decreased brown adipose tissue amount	Adgra1<tm1.1Zgwg>/Adgra1<tm1.1Zgwg>	Not Specified	N	33824276
MGI:7425250	M	MP:0005289	increased oxygen consumption	Adgra1<tm1.1Zgwg>/Adgra1<tm1.1Zgwg>	Not Specified	N	33824276
MGI:7425250	M	MP:0009133	decreased white fat cell size	Adgra1<tm1.1Zgwg>/Adgra1<tm1.1Zgwg>	Not Specified	N	33824276
MGI:7425250	M	MP:0011019	abnormal adaptive thermogenesis	Adgra1<tm1.1Zgwg>/Adgra1<tm1.1Zgwg>	Not Specified	N	33824276
MGI:7425250	M	MP:0008963	increased carbon dioxide production	Adgra1<tm1.1Zgwg>/Adgra1<tm1.1Zgwg>	Not Specified	N	33824276
MGI:7425250	M	MP:0013278	decreased fasting circulating glucose level	Adgra1<tm1.1Zgwg>/Adgra1<tm1.1Zgwg>	Not Specified	N	33824276
MGI:7425250	M	MP:0001262	decreased body weight	Adgra1<tm1.1Zgwg>/Adgra1<tm1.1Zgwg>	Not Specified	N	33824276
MGI:7425250	M	MP:0010025	decreased total body fat amount	Adgra1<tm1.1Zgwg>/Adgra1<tm1.1Zgwg>	Not Specified	N	33824276
MGI:7425250	M	MP:0004889	increased energy expenditure	Adgra1<tm1.1Zgwg>/Adgra1<tm1.1Zgwg>	Not Specified	N	33824276
MGI:7425250	M	MP:0003961	decreased lean body mass	Adgra1<tm1.1Zgwg>/Adgra1<tm1.1Zgwg>	Not Specified	N	33824276
MGI:7425250	M	MP:0003502	increased activity of thyroid gland	Adgra1<tm1.1Zgwg>/Adgra1<tm1.1Zgwg>	Not Specified	N	33824276
MGI:7425250	M	MP:0009125	decreased brown fat cell lipid droplet size	Adgra1<tm1.1Zgwg>/Adgra1<tm1.1Zgwg>	Not Specified	N	33824276
MGI:7427437	M	MP:0008898	abnormal acrosome morphology	Prss54<tm1Zgwg>/Prss54<tm1Zgwg>	involves: C57BL/6J * C57BL/6N	N	35863763
MGI:7427437	F	MP:0005389	reproductive system phenotype	Prss54<tm1Zgwg>/Prss54<tm1Zgwg>	involves: C57BL/6J * C57BL/6N	Y	35863763
MGI:7427437	M	MP:0001922	reduced male fertility	Prss54<tm1Zgwg>/Prss54<tm1Zgwg>	involves: C57BL/6J * C57BL/6N	N	35863763
MGI:7427437	M	MP:0030976	impaired sperm penetration of zona pellucida	Prss54<tm1Zgwg>/Prss54<tm1Zgwg>	involves: C57BL/6J * C57BL/6N	N	35863763
MGI:7427684	F	MP:0001923	reduced female fertility	Defb19<em1Cya>/Defb19<em1Cya>	C57BL/6-Defb19<em1Cya>	N	36513070
MGI:7427684	F	MP:0005410	abnormal fertilization	Defb19<em1Cya>/Defb19<em1Cya>	C57BL/6-Defb19<em1Cya>	N	36513070
MGI:7428307	M	MP:0009230	abnormal sperm head morphology	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0005384	cellular phenotype	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	Y	35950913
MGI:7428307	M	MP:0030949	abnormal Golgi vesicle transport	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0001925	male infertility	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0031355	abnormal proacrosomal vesicle fusion	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0004542	impaired acrosome reaction	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0009238	coiled sperm flagellum	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0009831	abnormal sperm midpiece morphology	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0008892	abnormal sperm flagellum morphology	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0030940	impaired autophagy	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0000242	impaired fertilization	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0002686	globozoospermia	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0008898	abnormal acrosome morphology	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0009235	small sperm head	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0002675	asthenozoospermia	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0011743	abnormal Golgi apparatus morphology	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0006380	abnormal spermatid morphology	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0031374	abnormal manchette assembly	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0020451	decreased sperm progressive motility	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0001932	abnormal spermiogenesis	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0009325	necrospermia	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0009376	abnormal manchette morphology	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0031388	absent manchette	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0009830	abnormal sperm connecting piece morphology	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0004884	abnormal testis physiology	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0009232	abnormal sperm nucleus morphology	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428307	M	MP:0031354	abnormal acrosome assembly	Pfn4<em1Hsc>/Pfn4<em1Hsc>	C57BL/6J-Pfn4<em1Hsc>	N	35950913
MGI:7428309	M	MP:0009325	necrospermia	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0009235	small sperm head	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0031374	abnormal manchette assembly	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0030949	abnormal Golgi vesicle transport	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0020451	decreased sperm progressive motility	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0002686	globozoospermia	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0004884	abnormal testis physiology	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0009232	abnormal sperm nucleus morphology	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0001932	abnormal spermiogenesis	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0031355	abnormal proacrosomal vesicle fusion	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0008898	abnormal acrosome morphology	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0002675	asthenozoospermia	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0011743	abnormal Golgi apparatus morphology	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0006380	abnormal spermatid morphology	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0009376	abnormal manchette morphology	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0009831	abnormal sperm midpiece morphology	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0001925	male infertility	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0009238	coiled sperm flagellum	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0008892	abnormal sperm flagellum morphology	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0000242	impaired fertilization	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0004542	impaired acrosome reaction	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0031354	abnormal acrosome assembly	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0005384	cellular phenotype	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	Y	35950913
MGI:7428309	M	MP:0031388	absent manchette	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0009830	abnormal sperm connecting piece morphology	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7428309	M	MP:0030940	impaired autophagy	Pfn4<em2Hsc>/Pfn4<em2Hsc>	C57BL/6J-Pfn4<em2Hsc>	N	35950913
MGI:7429209	M	MP:0002286	cryptorchism	Arb2a<Tg(Tyr)TpNpin>/Arb2a<Tg(Tyr)TpNpin>	involves: FVB/N	N	29311329
MGI:7429209	M	MP:0001157	small seminal vesicle	Arb2a<Tg(Tyr)TpNpin>/Arb2a<Tg(Tyr)TpNpin>	involves: FVB/N	N	29311329
MGI:7429209	F	MP:0009085	abnormal uterine horn morphology	Arb2a<Tg(Tyr)TpNpin>/Arb2a<Tg(Tyr)TpNpin>	involves: FVB/N	N	29311329
MGI:7429209	F	MP:0002636	delayed vaginal opening	Arb2a<Tg(Tyr)TpNpin>/Arb2a<Tg(Tyr)TpNpin>	involves: FVB/N	N	29311329
MGI:7429209	M	MP:0005188	small penis	Arb2a<Tg(Tyr)TpNpin>/Arb2a<Tg(Tyr)TpNpin>	involves: FVB/N	N	29311329
MGI:7430705	M	MP:0005389	reproductive system phenotype	Grm7<tm1Nak>/Grm7<tm1Nak>	B6.129P2-Grm7<tm1Nak>	Y	32865662
MGI:7430705	M	MP:0031628	abnormal intromission	Grm7<tm1Nak>/Grm7<tm1Nak>	B6.129P2-Grm7<tm1Nak>	N	32865662
MGI:7430705	M	MP:0001378	abnormal ejaculation	Grm7<tm1Nak>/Grm7<tm1Nak>	B6.129P2-Grm7<tm1Nak>	N	32865662
MGI:7430705	M	MP:0005386	behavior/neurological phenotype	Grm7<tm1Nak>/Grm7<tm1Nak>	B6.129P2-Grm7<tm1Nak>	Y	32865662
MGI:7430705	M	MP:0002566	abnormal sexual interaction	Grm7<tm1Nak>/Grm7<tm1Nak>	B6.129P2-Grm7<tm1Nak>	N	32865662
MGI:7430705	M	MP:0009856	failure of ejaculation	Grm7<tm1Nak>/Grm7<tm1Nak>	B6.129P2-Grm7<tm1Nak>	N	32865662
MGI:7430734	M	MP:0004852	decreased testis weight	Adamts16<em1(IMPC)H>/Adamts16<em1(IMPC)H>	C57BL/6NTac-Adamts16<em1(IMPC)H>	N	31748609
MGI:7431290	M	MP:0001559	hyperglycemia	Rr124128<tm1.1Jfer>/Rr124128<tm1.1Jfer>,Tg(Pdx1-cre)6Tuv/0	involves: C57BL/6 * FVB/N	N	36202974
MGI:7431290	M	MP:0005293	impaired glucose tolerance	Rr124128<tm1.1Jfer>/Rr124128<tm1.1Jfer>,Tg(Pdx1-cre)6Tuv/0	involves: C57BL/6 * FVB/N	N	36202974
MGI:7431290	M	MP:0002727	decreased circulating insulin level	Rr124128<tm1.1Jfer>/Rr124128<tm1.1Jfer>,Tg(Pdx1-cre)6Tuv/0	involves: C57BL/6 * FVB/N	N	36202974
MGI:7431292	M	MP:0002727	decreased circulating insulin level	Rr124128<tm1.2Jfer>/Rr124128<tm1.2Jfer>	involves: C57BL/6 * FVB/N	N	36202974
MGI:7431292	M	MP:0005293	impaired glucose tolerance	Rr124128<tm1.2Jfer>/Rr124128<tm1.2Jfer>	involves: C57BL/6 * FVB/N	N	36202974
MGI:7432893	M	MP:0001922	reduced male fertility	Misfa<em1Kei>/Misfa<em1Kei>	C57BL/6J-Misfa<em1Kei>	N	35228556
MGI:7432893	M	MP:0009647	decreased fertilization frequency	Misfa<em1Kei>/Misfa<em1Kei>	C57BL/6J-Misfa<em1Kei>	N	35228556
MGI:7432893	M	MP:0002675	asthenozoospermia	Misfa<em1Kei>/Misfa<em1Kei>	C57BL/6J-Misfa<em1Kei>	N	35228556
MGI:7432893	M	MP:0009237	kinked sperm flagellum	Misfa<em1Kei>/Misfa<em1Kei>	C57BL/6J-Misfa<em1Kei>	N	35228556
MGI:7432895	M	MP:0009647	decreased fertilization frequency	Misfa<em2Kei>/Misfa<em2Kei>	C57BL/6J-Misfa<em2Kei>	N	35228556
MGI:7432895	M	MP:0002675	asthenozoospermia	Misfa<em2Kei>/Misfa<em2Kei>	C57BL/6J-Misfa<em2Kei>	N	35228556
MGI:7432895	M	MP:0001922	reduced male fertility	Misfa<em2Kei>/Misfa<em2Kei>	C57BL/6J-Misfa<em2Kei>	N	35228556
MGI:7432897	M	MP:0014464	decreased sperm mitochondrial sheath size	Vdac3<em1Kei>/Vdac3<em1Kei>	C57BL/6J-Vdac3<em1Kei>	N	35228556
MGI:7432897	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Vdac3<em1Kei>/Vdac3<em1Kei>	C57BL/6J-Vdac3<em1Kei>	N	35228556
MGI:7432897	M	MP:0002675	asthenozoospermia	Vdac3<em1Kei>/Vdac3<em1Kei>	C57BL/6J-Vdac3<em1Kei>	N	35228556
MGI:7432897	M	MP:0001925	male infertility	Vdac3<em1Kei>/Vdac3<em1Kei>	C57BL/6J-Vdac3<em1Kei>	N	35228556
MGI:7432897	M	MP:0004852	decreased testis weight	Vdac3<em1Kei>/Vdac3<em1Kei>	C57BL/6J-Vdac3<em1Kei>	N	35228556
MGI:7432897	M	MP:0009647	decreased fertilization frequency	Vdac3<em1Kei>/Vdac3<em1Kei>	C57BL/6J-Vdac3<em1Kei>	N	35228556
MGI:7432897	M	MP:0009237	kinked sperm flagellum	Vdac3<em1Kei>/Vdac3<em1Kei>	C57BL/6J-Vdac3<em1Kei>	N	35228556
MGI:7432899	M	MP:0001922	reduced male fertility	Misfa<em5Kei>/Misfa<em5Kei>	C57BL/6J-Misfa<em5Kei>	N	35228556
MGI:7432899	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Misfa<em5Kei>/Misfa<em5Kei>	C57BL/6J-Misfa<em5Kei>	N	35228556
MGI:7432899	M	MP:0002675	asthenozoospermia	Misfa<em5Kei>/Misfa<em5Kei>	C57BL/6J-Misfa<em5Kei>	N	35228556
MGI:7432899	M	MP:0009647	decreased fertilization frequency	Misfa<em5Kei>/Misfa<em5Kei>	C57BL/6J-Misfa<em5Kei>	N	35228556
MGI:7432899	M	MP:0009237	kinked sperm flagellum	Misfa<em5Kei>/Misfa<em5Kei>	C57BL/6J-Misfa<em5Kei>	N	35228556
MGI:7434127	F	MP:0008876	decreased uterine NK cell number	Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	35194044
MGI:7434127	F	MP:0013401	increased endometrial gland number	Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	35194044
MGI:7434127	F	MP:0003845	abnormal decidualization	Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	35194044
MGI:7434127	F	MP:0001672	abnormal embryo development	Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	35194044
MGI:7434127	F	MP:0001712	abnormal placenta development	Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	35194044
MGI:7434127	F	MP:0031434	increased miscarriage rate	Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	35194044
MGI:7434127	F	MP:0001935	decreased litter size	Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	35194044
MGI:7434127	F	MP:0005033	abnormal trophoblast giant cell morphology	Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	35194044
MGI:7434127	F	MP:0001923	reduced female fertility	Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	35194044
MGI:7434127	F	MP:0008877	abnormal DNA methylation	Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	35194044
MGI:7434127	F	MP:0001729	impaired embryo implantation	Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	35194044
MGI:7434127	F	MP:0003984	embryonic growth retardation	Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Pgr<tm2(cre)Lyd>/Pgr<+>	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	N	35194044
MGI:7434319	M	MP:0014376	decreased miniature excitatory postsynaptic current frequency	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0003990	decreased neurotransmitter release	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0009538	abnormal synapse morphology	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0001900	impaired synaptic plasticity	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0003862	decreased aggression towards male mice	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0011448	decreased dopaminergic neuron number	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0001488	increased startle reflex	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0004792	abnormal synaptic vesicle number	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0001417	decreased exploration in new environment	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0004770	abnormal synaptic vesicle recycling	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0003088	abnormal prepulse inhibition	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0004793	abnormal synaptic vesicle clustering	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0020875	decreased nervous system dopamine level	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0002634	abnormal sensorimotor gating	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434319	M	MP:0001399	hyperactivity	Cdh2<em1Obir>/Cdh2<em1Obir>	C57BL/6JRcc-Cdh2<em1Obir>	N	34702855
MGI:7434354	M	MP:0001399	hyperactivity	Cdh2<em2Obir>/Cdh2<em2Obir>	C57BL/6JRcc-Cdh2<em2Obir>	N	34702855
MGI:7435338	M	MP:0005559	increased circulating glucose level	Lztfl1<tm1.3Zpl>/Lztfl1<tm1.3Zpl>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N	N	30423168
MGI:7435338	M	MP:0005293	impaired glucose tolerance	Lztfl1<tm1.3Zpl>/Lztfl1<tm1.3Zpl>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N	N	30423168
MGI:7435338	M	MP:0011939	increased food intake	Lztfl1<tm1.3Zpl>/Lztfl1<tm1.3Zpl>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N	N	30423168
MGI:7437739	M	MP:0005578	teratozoospermia	Cnih4<tm1a(EUCOMM)Hmgu>/Cnih4<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	36657507
MGI:7437739	M	MP:0002675	asthenozoospermia	Cnih4<tm1a(EUCOMM)Hmgu>/Cnih4<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	36657507
MGI:7437739	M	MP:0002687	oligozoospermia	Cnih4<tm1a(EUCOMM)Hmgu>/Cnih4<tm1a(EUCOMM)Hmgu>	involves: C57BL/6N	N	36657507
MGI:7438097	M	MP:0002675	asthenozoospermia	Odf4<em1Ktos>/Odf4<em1Ktos>	involves: C57BL/6J * DBA/2J	N	36804949
MGI:7438097	M	MP:0001922	reduced male fertility	Odf4<em1Ktos>/Odf4<em1Ktos>	involves: C57BL/6J * DBA/2J	N	36804949
MGI:7438097	M	MP:0009243	hairpin sperm flagellum	Odf4<em1Ktos>/Odf4<em1Ktos>	involves: C57BL/6J * DBA/2J	N	36804949
MGI:7438097	M	MP:0013286	abnormal sperm capacitation	Odf4<em1Ktos>/Odf4<em1Ktos>	involves: C57BL/6J * DBA/2J	N	36804949
MGI:7438097	M	MP:0008892	abnormal sperm flagellum morphology	Odf4<em1Ktos>/Odf4<em1Ktos>	involves: C57BL/6J * DBA/2J	N	36804949
MGI:7438097	M	MP:0002687	oligozoospermia	Odf4<em1Ktos>/Odf4<em1Ktos>	involves: C57BL/6J * DBA/2J	N	36804949
MGI:7438097	M	MP:0004852	decreased testis weight	Odf4<em1Ktos>/Odf4<em1Ktos>	involves: C57BL/6J * DBA/2J	N	36804949
MGI:7439373	M	MP:0014052	increased male germ cell apoptosis	Guf1<tm1.1Nju>/Guf1<tm1.1Nju>	involves: 129 * C57BL/6 * FVB/N	N	27065197
MGI:7439373	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Guf1<tm1.1Nju>/Guf1<tm1.1Nju>	involves: 129 * C57BL/6 * FVB/N	N	27065197
MGI:7439373	M	MP:0004852	decreased testis weight	Guf1<tm1.1Nju>/Guf1<tm1.1Nju>	involves: 129 * C57BL/6 * FVB/N	N	27065197
MGI:7439373	M	MP:0005132	decreased luteinizing hormone level	Guf1<tm1.1Nju>/Guf1<tm1.1Nju>	involves: 129 * C57BL/6 * FVB/N	N	27065197
MGI:7439373	M	MP:0005130	decreased follicle stimulating hormone level	Guf1<tm1.1Nju>/Guf1<tm1.1Nju>	involves: 129 * C57BL/6 * FVB/N	N	27065197
MGI:7439373	M	MP:0002687	oligozoospermia	Guf1<tm1.1Nju>/Guf1<tm1.1Nju>	involves: 129 * C57BL/6 * FVB/N	N	27065197
MGI:7439373	M	MP:0001925	male infertility	Guf1<tm1.1Nju>/Guf1<tm1.1Nju>	involves: 129 * C57BL/6 * FVB/N	N	27065197
MGI:7439373	M	MP:0002675	asthenozoospermia	Guf1<tm1.1Nju>/Guf1<tm1.1Nju>	involves: 129 * C57BL/6 * FVB/N	N	27065197
MGI:7439373	M	MP:0002781	increased circulating testosterone level	Guf1<tm1.1Nju>/Guf1<tm1.1Nju>	involves: 129 * C57BL/6 * FVB/N	N	27065197
MGI:7439373	M	MP:0001153	small seminiferous tubules	Guf1<tm1.1Nju>/Guf1<tm1.1Nju>	involves: 129 * C57BL/6 * FVB/N	N	27065197
MGI:7439373	M	MP:0001932	abnormal spermiogenesis	Guf1<tm1.1Nju>/Guf1<tm1.1Nju>	involves: 129 * C57BL/6 * FVB/N	N	27065197
MGI:7439374	M	MP:0004852	decreased testis weight	Guf1<tm1Nju>/Guf1<tm1Nju>,Alpl<tm1(cre)Nagy>/Alpl<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	27065197
MGI:7439374	M	MP:0001925	male infertility	Guf1<tm1Nju>/Guf1<tm1Nju>,Alpl<tm1(cre)Nagy>/Alpl<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	27065197
MGI:7439374	M	MP:0002687	oligozoospermia	Guf1<tm1Nju>/Guf1<tm1Nju>,Alpl<tm1(cre)Nagy>/Alpl<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	27065197
MGI:7439374	M	MP:0001153	small seminiferous tubules	Guf1<tm1Nju>/Guf1<tm1Nju>,Alpl<tm1(cre)Nagy>/Alpl<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	27065197
MGI:7439527	M	MP:0005605	increased bone mass	Rr383<tm1Caob>/Rr383<tm1Caob>	B6.Cg-Rr383<tm1Caob>	N	17932217
MGI:7439527	F	MP:0005605	increased bone mass	Rr383<tm1Caob>/Rr383<tm1Caob>	B6.Cg-Rr383<tm1Caob>	N	17932217
MGI:7439763	M	MP:0004852	decreased testis weight	Cep70<em1Qiao>/Cep70<em1Qiao>	C57BL/6J-Cep70<em1Qiao>	N	33980814
MGI:7439763	M	MP:0005159	azoospermia	Cep70<em1Qiao>/Cep70<em1Qiao>	C57BL/6J-Cep70<em1Qiao>	N	33980814
MGI:7439763	M	MP:0008279	arrest of spermiogenesis	Cep70<em1Qiao>/Cep70<em1Qiao>	C57BL/6J-Cep70<em1Qiao>	N	33980814
MGI:7439763	M	MP:0001925	male infertility	Cep70<em1Qiao>/Cep70<em1Qiao>	C57BL/6J-Cep70<em1Qiao>	N	33980814
MGI:7439763	M	MP:0001147	small testis	Cep70<em1Qiao>/Cep70<em1Qiao>	C57BL/6J-Cep70<em1Qiao>	N	33980814
MGI:7439763	M	MP:0009239	short sperm flagellum	Cep70<em1Qiao>/Cep70<em1Qiao>	C57BL/6J-Cep70<em1Qiao>	N	33980814
MGI:7439763	F	MP:0005389	reproductive system phenotype	Cep70<em1Qiao>/Cep70<em1Qiao>	C57BL/6J-Cep70<em1Qiao>	Y	33980814
MGI:7439763	M	MP:0009238	coiled sperm flagellum	Cep70<em1Qiao>/Cep70<em1Qiao>	C57BL/6J-Cep70<em1Qiao>	N	33980814
MGI:7439763	M	MP:0008898	abnormal acrosome morphology	Cep70<em1Qiao>/Cep70<em1Qiao>	C57BL/6J-Cep70<em1Qiao>	N	33980814
MGI:7439763	M	MP:0009235	small sperm head	Cep70<em1Qiao>/Cep70<em1Qiao>	C57BL/6J-Cep70<em1Qiao>	N	33980814
MGI:7439763	M	MP:0014052	increased male germ cell apoptosis	Cep70<em1Qiao>/Cep70<em1Qiao>	C57BL/6J-Cep70<em1Qiao>	N	33980814
MGI:7439763	M	MP:0005578	teratozoospermia	Cep70<em1Qiao>/Cep70<em1Qiao>	C57BL/6J-Cep70<em1Qiao>	N	33980814
MGI:7439763	M	MP:0009237	kinked sperm flagellum	Cep70<em1Qiao>/Cep70<em1Qiao>	C57BL/6J-Cep70<em1Qiao>	N	33980814
MGI:7441950	M	MP:0031010	failure of sperm-egg fusion	Fer1l5<tm1Osb>/Fer1l5<tm1Osb>	STOCK Fer1l5<tm1Osb>/75Osb	N	36696506
MGI:7441950	M	MP:0004542	impaired acrosome reaction	Fer1l5<tm1Osb>/Fer1l5<tm1Osb>	STOCK Fer1l5<tm1Osb>/75Osb	N	36696506
MGI:7441950	M	MP:0001922	reduced male fertility	Fer1l5<tm1Osb>/Fer1l5<tm1Osb>	STOCK Fer1l5<tm1Osb>/75Osb	N	36696506
MGI:7441950	M	MP:0030976	impaired sperm penetration of zona pellucida	Fer1l5<tm1Osb>/Fer1l5<tm1Osb>	STOCK Fer1l5<tm1Osb>/75Osb	N	36696506
MGI:7441950	F	MP:0005389	reproductive system phenotype	Fer1l5<tm1Osb>/Fer1l5<tm1Osb>	STOCK Fer1l5<tm1Osb>/75Osb	Y	36696506
MGI:7442184	M	MP:0001925	male infertility	Ccdc34<em1Fzg>/Ccdc34<em1Fzg>	C57BL/6-Ccdc34<em1Fzg>	N	34348960
MGI:7442184	M	MP:0031356	abnormal outer dense fiber morphology	Ccdc34<em1Fzg>/Ccdc34<em1Fzg>	C57BL/6-Ccdc34<em1Fzg>	N	34348960
MGI:7442184	M	MP:0014052	increased male germ cell apoptosis	Ccdc34<em1Fzg>/Ccdc34<em1Fzg>	C57BL/6-Ccdc34<em1Fzg>	N	34348960
MGI:7442184	M	MP:0002687	oligozoospermia	Ccdc34<em1Fzg>/Ccdc34<em1Fzg>	C57BL/6-Ccdc34<em1Fzg>	N	34348960
MGI:7442184	M	MP:0005578	teratozoospermia	Ccdc34<em1Fzg>/Ccdc34<em1Fzg>	C57BL/6-Ccdc34<em1Fzg>	N	34348960
MGI:7442184	M	MP:0009838	abnormal sperm axoneme morphology	Ccdc34<em1Fzg>/Ccdc34<em1Fzg>	C57BL/6-Ccdc34<em1Fzg>	N	34348960
MGI:7442184	M	MP:0002675	asthenozoospermia	Ccdc34<em1Fzg>/Ccdc34<em1Fzg>	C57BL/6-Ccdc34<em1Fzg>	N	34348960
MGI:7442184	F	MP:0005389	reproductive system phenotype	Ccdc34<em1Fzg>/Ccdc34<em1Fzg>	C57BL/6-Ccdc34<em1Fzg>	Y	34348960
MGI:7444103	M	MP:0005389	reproductive system phenotype	X/Prssly<em1Fjw>	C57BL/6-Prssly<em1Fjw>	Y	35485405
MGI:7444105	M	MP:0005389	reproductive system phenotype	X/Prssly<em2Fjw>	C57BL/6-Prssly<em2Fjw>	N	35485405
MGI:7444107	M	MP:0005389	reproductive system phenotype	Teyorf1<em1Fjw>/Teyorf1<em1Fjw>	C57BL/6-Teyorf1<em1Fjw>	N	35485405
MGI:7444109	M	MP:0005389	reproductive system phenotype	Teyorf1<em2Fjw>/Teyorf1<em2Fjw>	C57BL/6-Teyorf1<em2Fjw>	N	35485405
MGI:7444131	M	MP:0005389	reproductive system phenotype	X/Teyorf1<em3Fjw>	C57BL/6-Teyorf1<em3Fjw>	N	35485405
MGI:7444296	M	MP:0004901	decreased male germ cell number	Mlx<tm1.2Rne>/Mlx<tm1.2Rne>	involves: 129S4/SvJaeSor	N	34669700
MGI:7444296	M	MP:0004929	decreased epididymis weight	Mlx<tm1.2Rne>/Mlx<tm1.2Rne>	involves: 129S4/SvJaeSor	N	34669700
MGI:7444296	M	MP:0004852	decreased testis weight	Mlx<tm1.2Rne>/Mlx<tm1.2Rne>	involves: 129S4/SvJaeSor	N	34669700
MGI:7444296	M	MP:0002216	abnormal seminiferous tubule morphology	Mlx<tm1.2Rne>/Mlx<tm1.2Rne>	involves: 129S4/SvJaeSor	N	34669700
MGI:7444296	M	MP:0001925	male infertility	Mlx<tm1.2Rne>/Mlx<tm1.2Rne>	involves: 129S4/SvJaeSor	N	34669700
MGI:7444296	M	MP:0020450	abnormal sperm progressive motility	Mlx<tm1.2Rne>/Mlx<tm1.2Rne>	involves: 129S4/SvJaeSor	N	34669700
MGI:7444296	M	MP:0005578	teratozoospermia	Mlx<tm1.2Rne>/Mlx<tm1.2Rne>	involves: 129S4/SvJaeSor	N	34669700
MGI:7444296	M	MP:0002687	oligozoospermia	Mlx<tm1.2Rne>/Mlx<tm1.2Rne>	involves: 129S4/SvJaeSor	N	34669700
MGI:7444310	M	MP:0001925	male infertility	Mlx<tm1.1Rne>/Mlx<tm1.1Rne>,Tg(Amh-cre)8815Reb/0	involves: 129S4/SvJaeSor * FVB/N	N	34669700
MGI:7444310	M	MP:0002675	asthenozoospermia	Mlx<tm1.1Rne>/Mlx<tm1.1Rne>,Tg(Amh-cre)8815Reb/0	involves: 129S4/SvJaeSor * FVB/N	N	34669700
MGI:7444310	M	MP:0002687	oligozoospermia	Mlx<tm1.1Rne>/Mlx<tm1.1Rne>,Tg(Amh-cre)8815Reb/0	involves: 129S4/SvJaeSor * FVB/N	N	34669700
MGI:7444310	M	MP:0005578	teratozoospermia	Mlx<tm1.1Rne>/Mlx<tm1.1Rne>,Tg(Amh-cre)8815Reb/0	involves: 129S4/SvJaeSor * FVB/N	N	34669700
MGI:7444341	M	MP:0002216	abnormal seminiferous tubule morphology	Cep250<tm1b(EUCOMM)Wtsi>/Cep250<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	35599622
MGI:7444341	F	MP:0004856	decreased ovary weight	Cep250<tm1b(EUCOMM)Wtsi>/Cep250<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	35599622
MGI:7444341	M	MP:0001925	male infertility	Cep250<tm1b(EUCOMM)Wtsi>/Cep250<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	35599622
MGI:7444341	M	MP:0005159	azoospermia	Cep250<tm1b(EUCOMM)Wtsi>/Cep250<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	35599622
MGI:7444341	M	MP:0001153	small seminiferous tubules	Cep250<tm1b(EUCOMM)Wtsi>/Cep250<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	35599622
MGI:7444341	M	MP:0001147	small testis	Cep250<tm1b(EUCOMM)Wtsi>/Cep250<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	35599622
MGI:7444341	M	MP:0004901	decreased male germ cell number	Cep250<tm1b(EUCOMM)Wtsi>/Cep250<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	35599622
MGI:7444341	F	MP:0005431	decreased oocyte number	Cep250<tm1b(EUCOMM)Wtsi>/Cep250<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	35599622
MGI:7444341	F	MP:0001923	reduced female fertility	Cep250<tm1b(EUCOMM)Wtsi>/Cep250<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	35599622
MGI:7444341	M	MP:0005169	abnormal male meiosis	Cep250<tm1b(EUCOMM)Wtsi>/Cep250<tm1b(EUCOMM)Wtsi>	involves: C57BL/6N	N	35599622
MGI:7444373	M	MP:0002216	abnormal seminiferous tubule morphology	Cep250<tm1a(EUCOMM)Wtsi>/Cep250<tm1a(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N	N	35599622
MGI:7444373	M	MP:0001153	small seminiferous tubules	Cep250<tm1a(EUCOMM)Wtsi>/Cep250<tm1a(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N	N	35599622
MGI:7444373	M	MP:0001147	small testis	Cep250<tm1a(EUCOMM)Wtsi>/Cep250<tm1a(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N	N	35599622
MGI:7444373	M	MP:0004901	decreased male germ cell number	Cep250<tm1a(EUCOMM)Wtsi>/Cep250<tm1a(EUCOMM)Wtsi>,Tg(Stra8-icre)1Reb/0	involves: C57BL/6N	N	35599622
MGI:7444811	M	MP:0009238	coiled sperm flagellum	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0002216	abnormal seminiferous tubule morphology	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0001147	small testis	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0004852	decreased testis weight	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0009243	hairpin sperm flagellum	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0005169	abnormal male meiosis	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0009234	absent sperm head	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0020451	decreased sperm progressive motility	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0001922	reduced male fertility	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0013288	premature acrosome reaction	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0020550	multinucleated giant male germ cells	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0005578	teratozoospermia	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0002687	oligozoospermia	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0014052	increased male germ cell apoptosis	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444811	M	MP:0008898	abnormal acrosome morphology	Hadh<em1Jgao>/Hadh<em1Jgao>	Not Specified	N	36398584
MGI:7444965	M	MP:0009647	decreased fertilization frequency	Cep78<em2Gpt>/Cep78<em2Gpt>	C57BL/6JGpt-Cep78<em2Gpt>	N	36206347
MGI:7444965	M	MP:0008545	absent sperm flagellum	Cep78<em2Gpt>/Cep78<em2Gpt>	C57BL/6JGpt-Cep78<em2Gpt>	N	36206347
MGI:7444965	M	MP:0009838	abnormal sperm axoneme morphology	Cep78<em2Gpt>/Cep78<em2Gpt>	C57BL/6JGpt-Cep78<em2Gpt>	N	36206347
MGI:7444965	M	MP:0009230	abnormal sperm head morphology	Cep78<em2Gpt>/Cep78<em2Gpt>	C57BL/6JGpt-Cep78<em2Gpt>	N	36206347
MGI:7444965	M	MP:0005578	teratozoospermia	Cep78<em2Gpt>/Cep78<em2Gpt>	C57BL/6JGpt-Cep78<em2Gpt>	N	36206347
MGI:7444965	M	MP:0009831	abnormal sperm midpiece morphology	Cep78<em2Gpt>/Cep78<em2Gpt>	C57BL/6JGpt-Cep78<em2Gpt>	N	36206347
MGI:7444965	M	MP:0009239	short sperm flagellum	Cep78<em2Gpt>/Cep78<em2Gpt>	C57BL/6JGpt-Cep78<em2Gpt>	N	36206347
MGI:7444965	M	MP:0001925	male infertility	Cep78<em2Gpt>/Cep78<em2Gpt>	C57BL/6JGpt-Cep78<em2Gpt>	N	36206347
MGI:7444965	M	MP:0002675	asthenozoospermia	Cep78<em2Gpt>/Cep78<em2Gpt>	C57BL/6JGpt-Cep78<em2Gpt>	N	36206347
MGI:7444965	M	MP:0002687	oligozoospermia	Cep78<em2Gpt>/Cep78<em2Gpt>	C57BL/6JGpt-Cep78<em2Gpt>	N	36206347
MGI:7444965	M	MP:0008892	abnormal sperm flagellum morphology	Cep78<em2Gpt>/Cep78<em2Gpt>	C57BL/6JGpt-Cep78<em2Gpt>	N	36206347
MGI:7446675	M	MP:0031391	increased locomotor activity	Wdr3<tm1a(KOMP)Wtsi>/Wdr3<+>	C57BL/6N-Wdr3<tm1a(KOMP)Wtsi>	N	36463953
MGI:7446675	M	MP:0003631	nervous system phenotype	Wdr3<tm1a(KOMP)Wtsi>/Wdr3<+>	C57BL/6N-Wdr3<tm1a(KOMP)Wtsi>	Y	36463953
MGI:7446675	M	MP:0005378	growth/size/body region phenotype	Wdr3<tm1a(KOMP)Wtsi>/Wdr3<+>	C57BL/6N-Wdr3<tm1a(KOMP)Wtsi>	Y	36463953
MGI:7446675	M	MP:0005391	vision/eye phenotype	Wdr3<tm1a(KOMP)Wtsi>/Wdr3<+>	C57BL/6N-Wdr3<tm1a(KOMP)Wtsi>	Y	36463953
MGI:7446675	M	MP:0005386	behavior/neurological phenotype	Wdr3<tm1a(KOMP)Wtsi>/Wdr3<+>	C57BL/6N-Wdr3<tm1a(KOMP)Wtsi>	Y	36463953
MGI:7447472	M	MP:0004901	decreased male germ cell number	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0002660	abnormal caput epididymis morphology	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0004542	impaired acrosome reaction	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0001935	decreased litter size	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0001922	reduced male fertility	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0020451	decreased sperm progressive motility	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0000242	impaired fertilization	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0009647	decreased fertilization frequency	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0004884	abnormal testis physiology	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0001147	small testis	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0010954	abnormal cellular respiration	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0010959	abnormal oxidative phosphorylation	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0030978	impaired binding of sperm to zona pellucida	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0013601	increased testis apoptosis	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0002675	asthenozoospermia	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	F	MP:0001729	impaired embryo implantation	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0002687	oligozoospermia	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	F	MP:0005389	reproductive system phenotype	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	Y	36331537
MGI:7447472	M	MP:0004543	abnormal sperm physiology	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0001932	abnormal spermiogenesis	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7447472	M	MP:0001156	abnormal spermatogenesis	4930590J08Rik<em1Qsh>/4930590J08Rik<em1Qsh>	C57BL/6-4930590J08Rik<em1Qsh>	N	36331537
MGI:7448449	M	MP:0005389	reproductive system phenotype	Lypd4<em1Eyx>/Lypd4<em1Eyx>	involves: C57BL/6N	Y	32040177
MGI:7448449	M	MP:0031012	impaired sperm migration in female genital tract	Lypd4<em1Eyx>/Lypd4<em1Eyx>	involves: C57BL/6N	N	32040177
MGI:7448449	M	MP:0009647	decreased fertilization frequency	Lypd4<em1Eyx>/Lypd4<em1Eyx>	involves: C57BL/6N	N	32040177
MGI:7448449	M	MP:0030978	impaired binding of sperm to zona pellucida	Lypd4<em1Eyx>/Lypd4<em1Eyx>	involves: C57BL/6N	N	32040177
MGI:7448449	M	MP:0000242	impaired fertilization	Lypd4<em1Eyx>/Lypd4<em1Eyx>	involves: C57BL/6N	N	32040177
MGI:7448449	M	MP:0004543	abnormal sperm physiology	Lypd4<em1Eyx>/Lypd4<em1Eyx>	involves: C57BL/6N	N	32040177
MGI:7448449	M	MP:0001925	male infertility	Lypd4<em1Eyx>/Lypd4<em1Eyx>	involves: C57BL/6N	N	32040177
MGI:7448527	M	MP:0001156	abnormal spermatogenesis	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448527	M	MP:0006035	abnormal mitochondrial morphology	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448527	M	MP:0001154	seminiferous tubule degeneration	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448527	M	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448527	M	MP:0020362	abnormal male germ cell physiology	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448527	M	MP:0005384	cellular phenotype	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	Y	33674260
MGI:7448527	M	MP:0006362	abnormal male germ cell morphology	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448527	M	MP:0004930	small epididymis	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448527	M	MP:0001147	small testis	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448527	M	MP:0004852	decreased testis weight	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448527	M	MP:0002687	oligozoospermia	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448527	M	MP:0030937	increased mitochondrial DNA content	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448527	M	MP:0006038	increased mitochondrial fission	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448527	M	MP:0001925	male infertility	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0005578	teratozoospermia	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0009238	coiled sperm flagellum	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0014052	increased male germ cell apoptosis	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0004901	decreased male germ cell number	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0006038	increased mitochondrial fission	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0001156	abnormal spermatogenesis	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0001147	small testis	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0013601	increased testis apoptosis	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0001154	seminiferous tubule degeneration	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0002687	oligozoospermia	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0001925	male infertility	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0004852	decreased testis weight	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0001153	small seminiferous tubules	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0006035	abnormal mitochondrial morphology	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0004930	small epididymis	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0006380	abnormal spermatid morphology	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0006379	abnormal spermatocyte morphology	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0030937	increased mitochondrial DNA content	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0020362	abnormal male germ cell physiology	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0009234	absent sperm head	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0006362	abnormal male germ cell morphology	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0009378	abnormal endoplasmic reticulum morphology	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0009230	abnormal sperm head morphology	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448528	M	MP:0005384	cellular phenotype	Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	Y	33674260
MGI:7448532	M	MP:0004930	small epididymis	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448532	M	MP:0006035	abnormal mitochondrial morphology	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448532	M	MP:0001154	seminiferous tubule degeneration	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448532	M	MP:0004901	decreased male germ cell number	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448532	M	MP:0006379	abnormal spermatocyte morphology	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448532	M	MP:0001156	abnormal spermatogenesis	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448532	M	MP:0001147	small testis	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448532	M	MP:0006380	abnormal spermatid morphology	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448532	M	MP:0008261	arrest of male meiosis	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448532	M	MP:0001153	small seminiferous tubules	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448532	M	MP:0001925	male infertility	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448532	M	MP:0004852	decreased testis weight	Mfn1<tm2Dcc>/Mfn1<tm2Dcc>,Mfn2<tm3Dcc>/Mfn2<tm3Dcc>,Tg(Stra8-icre)1Reb/0	involves: 129 * C57BL/6J * FVB/NJ	N	33674260
MGI:7448597	F	MP:0001127	small ovary	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448597	M	MP:0005376	homeostasis/metabolism phenotype	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	Y	36613635
MGI:7448597	M	MP:0001153	small seminiferous tubules	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448597	M	MP:0003642	absent seminal vesicle	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448597	M	MP:0001925	male infertility	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448597	M	MP:0005188	small penis	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448597	M	MP:0005379	endocrine/exocrine gland phenotype	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	Y	36613635
MGI:7448597	M	MP:0001147	small testis	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448597	F	MP:0001926	female infertility	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448597	M	MP:0002687	oligozoospermia	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448597	M	MP:0012225	decreased sterol level	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448597	F	MP:0002790	decreased circulating follicle stimulating hormone level	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448597	M	MP:0005389	reproductive system phenotype	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	Y	36613635
MGI:7448597	F	MP:0001130	abnormal ovarian folliculogenesis	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448597	M	MP:0002786	abnormal Leydig cell morphology	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448597	F	MP:0002680	decreased corpora lutea number	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448597	M	MP:0020824	abnormal testis tissue architecture	Rr401<em1Yushi>/Rr401<em1Yushi>	Not Specified	N	36613635
MGI:7448875	M	MP:0001364	decreased anxiety-related response	Rr364729<em1Almk>/Rr364729<em1Almk>	C57BL/6-Rr364729<em1Almk>	N	32203157
MGI:7450820	M	MP:0008261	arrest of male meiosis	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	M	MP:0008967	absent chiasmata formation	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	F	MP:0005168	abnormal female meiosis	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	F	MP:0008995	early reproductive senescence	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	F	MP:0001923	reduced female fertility	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	M	MP:0004852	decreased testis weight	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	F	MP:0020364	abnormal female germ cell physiology	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	M	MP:0002216	abnormal seminiferous tubule morphology	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	M	MP:0006379	abnormal spermatocyte morphology	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	F	MP:0009451	abnormal chromosomal synapsis	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	F	MP:0005431	decreased oocyte number	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	M	MP:0005169	abnormal male meiosis	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	M	MP:0001925	male infertility	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450820	M	MP:0014052	increased male germ cell apoptosis	Ankrd31<em1Atot>/Ankrd31<em1Atot>	involves: C57BL/6J	N	31000436
MGI:7450822	F	MP:0001923	reduced female fertility	Ankrd31<em2Atot>/Ankrd31<em2Atot>	involves: C57BL/6J	N	31000436
MGI:7450822	M	MP:0001925	male infertility	Ankrd31<em2Atot>/Ankrd31<em2Atot>	involves: C57BL/6J	N	31000436
MGI:7450849	M	MP:0005377	hearing/vestibular/ear phenotype	Diaph2<em2Kcl>/Y	C57BL/6J-Diaph2<em2Kcl>	N	36689403
MGI:7450851	F	MP:0005377	hearing/vestibular/ear phenotype	Diaph2<em1Kcl>/Diaph2<em1Kcl>	C57BL/6J-Diaph2<em1Kcl>	N	36689403
MGI:7450853	M	MP:0005377	hearing/vestibular/ear phenotype	Diaph2<em1Kcl>/Y	C57BL/6J-Diaph2<em1Kcl>	N	36689403
MGI:7450854	F	MP:0005377	hearing/vestibular/ear phenotype	Diaph2<em2Kcl>/Diaph2<em2Kcl>	C57BL/6J-Diaph2<em2Kcl>	Y	36689403
MGI:7450862	M	MP:0005389	reproductive system phenotype	Mageb5b<em1Jbmu> Del(XMageb5)1Jbmu/Y	B6(SJL)-Mageb5b<em1Jbmu> Del(XMageb5)1Jbmu/Jbmu	Y	35595785
MGI:7450862	M	MP:0005578	teratozoospermia	Mageb5b<em1Jbmu> Del(XMageb5)1Jbmu/Y	B6(SJL)-Mageb5b<em1Jbmu> Del(XMageb5)1Jbmu/Jbmu	N	35595785
MGI:7450863	M	MP:0005578	teratozoospermia	Mageb5b<em2Jbmu> Del(XMageb5)1Jbmu/Y	B6(SJL)-Mageb5b<em2Jbmu> Del(XMageb5)1Jbmu/Jbmu	N	35595785
MGI:7450863	M	MP:0005389	reproductive system phenotype	Mageb5b<em2Jbmu> Del(XMageb5)1Jbmu/Y	B6(SJL)-Mageb5b<em2Jbmu> Del(XMageb5)1Jbmu/Jbmu	N	35595785
MGI:7450865	M	MP:0005389	reproductive system phenotype	4930567H17Rik<em1Jbmu> Gm14725<em1Jbmu>/Y	B6(SJL)-4930567H17Rik<em1Jbmu> Gm14725<em1Jbmu>/Jbmu	Y	35595785
MGI:7450865	M	MP:0005578	teratozoospermia	4930567H17Rik<em1Jbmu> Gm14725<em1Jbmu>/Y	B6(SJL)-4930567H17Rik<em1Jbmu> Gm14725<em1Jbmu>/Jbmu	N	35595785
MGI:7450942	M	MP:0004852	decreased testis weight	Adad2<em1Shnk>/Adad2<em1Shnk>	C57BL/6-Adad2<em1Shnk>	N	36930220
MGI:7450942	M	MP:0008279	arrest of spermiogenesis	Adad2<em1Shnk>/Adad2<em1Shnk>	C57BL/6-Adad2<em1Shnk>	N	36930220
MGI:7450942	M	MP:0005169	abnormal male meiosis	Adad2<em1Shnk>/Adad2<em1Shnk>	C57BL/6-Adad2<em1Shnk>	N	36930220
MGI:7450942	M	MP:0008898	abnormal acrosome morphology	Adad2<em1Shnk>/Adad2<em1Shnk>	C57BL/6-Adad2<em1Shnk>	N	36930220
MGI:7450942	M	MP:0001925	male infertility	Adad2<em1Shnk>/Adad2<em1Shnk>	C57BL/6-Adad2<em1Shnk>	N	36930220
MGI:7450942	M	MP:0005159	azoospermia	Adad2<em1Shnk>/Adad2<em1Shnk>	C57BL/6-Adad2<em1Shnk>	N	36930220
MGI:7450944	M	MP:0008898	abnormal acrosome morphology	Adad2<em2Shnk>/Adad2<em2Shnk>	C57BL/6-Adad2<em2Shnk>	N	36930220
MGI:7450944	M	MP:0008279	arrest of spermiogenesis	Adad2<em2Shnk>/Adad2<em2Shnk>	C57BL/6-Adad2<em2Shnk>	N	36930220
MGI:7450944	M	MP:0004852	decreased testis weight	Adad2<em2Shnk>/Adad2<em2Shnk>	C57BL/6-Adad2<em2Shnk>	N	36930220
MGI:7450944	M	MP:0005169	abnormal male meiosis	Adad2<em2Shnk>/Adad2<em2Shnk>	C57BL/6-Adad2<em2Shnk>	N	36930220
MGI:7450944	M	MP:0001925	male infertility	Adad2<em2Shnk>/Adad2<em2Shnk>	C57BL/6-Adad2<em2Shnk>	N	36930220
MGI:7450944	M	MP:0005159	azoospermia	Adad2<em2Shnk>/Adad2<em2Shnk>	C57BL/6-Adad2<em2Shnk>	N	36930220
MGI:7451460	M	MP:0010024	increased total body fat amount	Micu1<tm1bNarl>/Micu1<+>	C57BL/6N-Micu1<tm1bNarl>/Narl	N	MGI:5576271
MGI:7451461	M	MP:0005343	increased circulating aspartate transaminase level	Polr1d<em1(IMPC)J>/Polr1d<+>	C57BL/6NJ-Polr1d<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7464253	M	MP:0008261	arrest of male meiosis	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0004852	decreased testis weight	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0001932	abnormal spermiogenesis	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0031374	abnormal manchette assembly	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0009376	abnormal manchette morphology	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0004024	aneuploidy	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0009761	abnormal meiotic spindle morphology	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0014052	increased male germ cell apoptosis	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0010948	abnormal double-strand DNA break repair	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	F	MP:0005389	reproductive system phenotype	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	Y	36971361
MGI:7464253	M	MP:0001154	seminiferous tubule degeneration	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0031375	abnormal manchette disassembly	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0009232	abnormal sperm nucleus morphology	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0031386	elongated manchette	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0005169	abnormal male meiosis	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0001147	small testis	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0001156	abnormal spermatogenesis	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0031354	abnormal acrosome assembly	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0001925	male infertility	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0005159	azoospermia	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0008898	abnormal acrosome morphology	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0006380	abnormal spermatid morphology	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464253	M	MP:0009377	ectopic manchette	Spast<tm1a(KOMP)Wtsi>/Spast<tm1a(KOMP)Wtsi>	involves: C57BL/6N	N	36971361
MGI:7464535	F	MP:0001325	abnormal retina morphology	mrs1/mrs1	B6.Cg-mrs1/BocJ	N	MGI:7464180
MGI:7464535	F	MP:0003733	abnormal retina inner nuclear layer morphology	mrs1/mrs1	B6.Cg-mrs1/BocJ	N	MGI:7464180
MGI:7464535	F	MP:0031198	retina inner nuclear layer degeneration	mrs1/mrs1	B6.Cg-mrs1/BocJ	N	MGI:7464180
MGI:7464784	F	MP:0000484	abnormal pulmonary artery morphology	Atl1<tm1.1Cbla>/Atl1<tm1.1Cbla>,Reep1<Gt(OST398247)Tigm>/Reep1<Gt(OST398247)Tigm>	B6.Cg-Reep1<Gt(OST398247)Tigm> Atl1<tm1.1Cbla>	N	35348668
MGI:7465132	M	MP:0010932	increased trabecular bone connectivity density	Lgals3<em1Vari>/Lgals3<em1Vari>	involves: C3H/HeJ * C57BL/6J	N	36062328
MGI:7465132	M	MP:0013620	increased internal diameter of femur	Lgals3<em1Vari>/Lgals3<em1Vari>	involves: C3H/HeJ * C57BL/6J	N	36062328
MGI:7465132	F	MP:0013615	increased volumetric bone mineral density	Lgals3<em1Vari>/Lgals3<em1Vari>	involves: C3H/HeJ * C57BL/6J	N	36062328
MGI:7465132	M	MP:0004991	decreased bone strength	Lgals3<em1Vari>/Lgals3<em1Vari>	involves: C3H/HeJ * C57BL/6J	N	36062328
MGI:7465132	F	MP:0010868	increased bone trabecula number	Lgals3<em1Vari>/Lgals3<em1Vari>	involves: C3H/HeJ * C57BL/6J	N	36062328
MGI:7465132	F	MP:0010872	increased trabecular bone mass	Lgals3<em1Vari>/Lgals3<em1Vari>	involves: C3H/HeJ * C57BL/6J	N	36062328
MGI:7465132	M	MP:0010875	increased bone volume	Lgals3<em1Vari>/Lgals3<em1Vari>	involves: C3H/HeJ * C57BL/6J	N	36062328
MGI:7465132	F	MP:0010878	increased trabecular bone volume	Lgals3<em1Vari>/Lgals3<em1Vari>	involves: C3H/HeJ * C57BL/6J	N	36062328
MGI:7465132	F	MP:0009347	increased trabecular bone thickness	Lgals3<em1Vari>/Lgals3<em1Vari>	involves: C3H/HeJ * C57BL/6J	N	36062328
MGI:7465132	F	MP:0005390	skeleton phenotype	Lgals3<em1Vari>/Lgals3<em1Vari>	involves: C3H/HeJ * C57BL/6J	Y	36062328
MGI:7465132	F	MP:0013631	decreased bone trabecular spacing	Lgals3<em1Vari>/Lgals3<em1Vari>	involves: C3H/HeJ * C57BL/6J	N	36062328
MGI:7465132	F	MP:0021187	increased bone mineral density of vertebrae	Lgals3<em1Vari>/Lgals3<em1Vari>	involves: C3H/HeJ * C57BL/6J	N	36062328
MGI:7465132	M	MP:0010964	increased compact bone volume	Lgals3<em1Vari>/Lgals3<em1Vari>	involves: C3H/HeJ * C57BL/6J	N	36062328
MGI:7465150	M	MP:0031198	retina inner nuclear layer degeneration	mrs1/Y	B6.Cg-mrs1/BocJ	N	MGI:7464180
MGI:7465150	M	MP:0003733	abnormal retina inner nuclear layer morphology	mrs1/Y	B6.Cg-mrs1/BocJ	N	MGI:7464180
MGI:7465150	M	MP:0001325	abnormal retina morphology	mrs1/Y	B6.Cg-mrs1/BocJ	N	MGI:7464180
MGI:7466577	M	MP:0008489	slow postnatal weight gain	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	N	34549824
MGI:7466577	M	MP:0003887	increased hepatocyte apoptosis	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	N	34549824
MGI:7466577	M	MP:0000602	dilated liver sinusoidal space	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	N	34549824
MGI:7466577	M	MP:0001262	decreased body weight	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	N	34549824
MGI:7466577	M	MP:0005378	growth/size/body region phenotype	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	Y	34549824
MGI:7466577	M	MP:0031265	increased susceptibility to hepatic steatosis	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	N	34549824
MGI:7466577	M	MP:0005370	liver/biliary system phenotype	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	Y	34549824
MGI:7466577	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	N	34549824
MGI:7466577	M	MP:0031271	increased susceptibility to age-related hepatic steatosis	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	N	34549824
MGI:7466577	M	MP:0020354	increased endoplasmic reticulum stress	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	N	34549824
MGI:7466577	M	MP:0005331	insulin resistance	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	N	34549824
MGI:7466577	M	MP:0003402	decreased liver weight	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	N	34549824
MGI:7466577	M	MP:0020582	increased ceramide level	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	N	34549824
MGI:7466577	M	MP:0000607	abnormal hepatocyte morphology	Creld2<tm1.1Emass>/Creld2<tm1.1Emass>	B6.129P2(SJL)-Creld2<tm1.1Emass>	N	34549824
MGI:7469827	M	MP:0010124	decreased bone mineral content	Tbl1xr1<em2H>/Tbl1xr1<em2H>	C57BL/6J-Tbl1xr1<em2H>	N	35416977
MGI:7469827	M	MP:0001262	decreased body weight	Tbl1xr1<em2H>/Tbl1xr1<em2H>	C57BL/6J-Tbl1xr1<em2H>	N	35416977
MGI:7470912	M	MP:0031012	impaired sperm migration in female genital tract	Nicol1<em1Osb>/Nicol1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	37095084
MGI:7470912	M	MP:0030978	impaired binding of sperm to zona pellucida	Nicol1<em1Osb>/Nicol1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	37095084
MGI:7470912	F	MP:0005389	reproductive system phenotype	Nicol1<em1Osb>/Nicol1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	37095084
MGI:7470912	M	MP:0004935	epididymis degeneration	Nicol1<em1Osb>/Nicol1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	37095084
MGI:7470912	M	MP:0009647	decreased fertilization frequency	Nicol1<em1Osb>/Nicol1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	37095084
MGI:7470912	M	MP:0001925	male infertility	Nicol1<em1Osb>/Nicol1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	37095084
MGI:7471846	M	MP:0000274	enlarged heart	0610040J01Rik<em1(IMPC)Ccpcz>/0610040J01Rik<em1(IMPC)Ccpcz>	C57BL/6NCrl-0610040J01Rik<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471846	M	MP:0000692	small spleen	0610040J01Rik<em1(IMPC)Ccpcz>/0610040J01Rik<em1(IMPC)Ccpcz>	C57BL/6NCrl-0610040J01Rik<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471846	M	MP:0000266	abnormal heart morphology	0610040J01Rik<em1(IMPC)Ccpcz>/0610040J01Rik<em1(IMPC)Ccpcz>	C57BL/6NCrl-0610040J01Rik<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471847	F	MP:0000709	enlarged thymus	Abca5<em1(IMPC)Ccpcz>/Abca5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Abca5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471847	M	MP:0000266	abnormal heart morphology	Abca5<em1(IMPC)Ccpcz>/Abca5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Abca5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471847	F	MP:0002060	abnormal skin morphology	Abca5<em1(IMPC)Ccpcz>/Abca5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Abca5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471847	M	MP:0002135	abnormal kidney morphology	Abca5<em1(IMPC)Ccpcz>/Abca5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Abca5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471847	F	MP:0000703	abnormal thymus morphology	Abca5<em1(IMPC)Ccpcz>/Abca5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Abca5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471847	M	MP:0003068	enlarged kidney	Abca5<em1(IMPC)Ccpcz>/Abca5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Abca5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471847	M	MP:0000274	enlarged heart	Abca5<em1(IMPC)Ccpcz>/Abca5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Abca5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471848	M	MP:0000274	enlarged heart	Ace2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Ace2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471848	M	MP:0000266	abnormal heart morphology	Ace2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Ace2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471848	M	MP:0000691	enlarged spleen	Ace2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Ace2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471848	M	MP:0000689	abnormal spleen morphology	Ace2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Ace2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471849	F	MP:0001120	abnormal uterus morphology	Ace2<em1(IMPC)Ccpcz>/Ace2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ace2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471849	F	MP:0003961	decreased lean body mass	Ace2<em1(IMPC)Ccpcz>/Ace2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ace2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471849	F	MP:0009709	hydrometra	Ace2<em1(IMPC)Ccpcz>/Ace2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ace2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471849	F	MP:0010024	increased total body fat amount	Ace2<em1(IMPC)Ccpcz>/Ace2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ace2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471849	F	MP:0000691	enlarged spleen	Ace2<em1(IMPC)Ccpcz>/Ace2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ace2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471849	F	MP:0000703	abnormal thymus morphology	Ace2<em1(IMPC)Ccpcz>/Ace2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ace2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471849	F	MP:0000689	abnormal spleen morphology	Ace2<em1(IMPC)Ccpcz>/Ace2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ace2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471849	F	MP:0001325	abnormal retina morphology	Ace2<em1(IMPC)Ccpcz>/Ace2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ace2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471849	F	MP:0000709	enlarged thymus	Ace2<em1(IMPC)Ccpcz>/Ace2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ace2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471850	M	MP:0001257	increased body length	Acot8<em1(IMPC)Bay>/Acot8<em1(IMPC)Bay>	C57BL/6N-Acot8<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471851	F	MP:0008810	increased circulating iron level	Acsf3<em1(IMPC)Hmgu>/Acsf3<em1(IMPC)Hmgu>	C57BL/6NCrl-Acsf3<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471852	M	MP:0005011	increased eosinophil cell number	Acsm1<em1(IMPC)Mhzh>/Acsm1<em1(IMPC)Mhzh>	C57BL/6N-Acsm1<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7471854	M	MP:0004156	abnormal QT variability	Aff2<em1(IMPC)Hmgu>/Y	C57BL/6NCrl-Aff2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471855	M	MP:0001399	hyperactivity	Afg1l<em1(IMPC)Kmpc>/Afg1l<em1(IMPC)Kmpc>	C57BL/6NTac-Afg1l<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471855	M	MP:0002833	increased heart weight	Afg1l<em1(IMPC)Kmpc>/Afg1l<em1(IMPC)Kmpc>	C57BL/6NTac-Afg1l<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471855	M	MP:0000367	abnormal coat/ hair morphology	Afg1l<em1(IMPC)Kmpc>/Afg1l<em1(IMPC)Kmpc>	C57BL/6NTac-Afg1l<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471855	M	MP:0002075	abnormal coat/hair pigmentation	Afg1l<em1(IMPC)Kmpc>/Afg1l<em1(IMPC)Kmpc>	C57BL/6NTac-Afg1l<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471856	F	MP:0010052	increased grip strength	Agbl2<em1(IMPC)H>/Agbl2<em1(IMPC)H>	C57BL/6NTac-Agbl2<em1(IMPC)H>/H	N	MGI:5576271
MGI:7471858	M	MP:0003271	abnormal duodenum morphology	Ak4<em1(IMPC)Kmpc>/Ak4<em1(IMPC)Kmpc>	C57BL/6NTac-Ak4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471858	M	MP:0002581	abnormal ileum morphology	Ak4<em1(IMPC)Kmpc>/Ak4<em1(IMPC)Kmpc>	C57BL/6NTac-Ak4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471858	M	MP:0002059	abnormal seminal vesicle morphology	Ak4<em1(IMPC)Kmpc>/Ak4<em1(IMPC)Kmpc>	C57BL/6NTac-Ak4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471858	M	MP:0000367	abnormal coat/ hair morphology	Ak4<em1(IMPC)Kmpc>/Ak4<em1(IMPC)Kmpc>	C57BL/6NTac-Ak4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471858	M	MP:0005178	increased circulating cholesterol level	Ak4<em1(IMPC)Kmpc>/Ak4<em1(IMPC)Kmpc>	C57BL/6NTac-Ak4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471858	M	MP:0002075	abnormal coat/hair pigmentation	Ak4<em1(IMPC)Kmpc>/Ak4<em1(IMPC)Kmpc>	C57BL/6NTac-Ak4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471858	M	MP:0000182	increased circulating LDL cholesterol level	Ak4<em1(IMPC)Kmpc>/Ak4<em1(IMPC)Kmpc>	C57BL/6NTac-Ak4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471858	M	MP:0010123	increased bone mineral content	Ak4<em1(IMPC)Kmpc>/Ak4<em1(IMPC)Kmpc>	C57BL/6NTac-Ak4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471859	F	MP:0002100	abnormal tooth morphology	Amelx<em1(IMPC)Ccpcz>/Amelx<+>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471859	F	MP:0000702	enlarged lymph nodes	Amelx<em1(IMPC)Ccpcz>/Amelx<+>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471859	F	MP:0005011	increased eosinophil cell number	Amelx<em1(IMPC)Ccpcz>/Amelx<+>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471859	F	MP:0005016	decreased lymphocyte cell number	Amelx<em1(IMPC)Ccpcz>/Amelx<+>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471859	F	MP:0003036	vertebral transformation	Amelx<em1(IMPC)Ccpcz>/Amelx<+>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471859	F	MP:0002339	abnormal lymph node morphology	Amelx<em1(IMPC)Ccpcz>/Amelx<+>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471859	F	MP:0004599	abnormal vertebral arch morphology	Amelx<em1(IMPC)Ccpcz>/Amelx<+>	C57BL/6N-Amelx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471860	F	MP:0010053	decreased grip strength	Anapc5<em1(IMPC)Bay>/Anapc5<+>	C57BL/6N-Anapc5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471862	F	MP:0010053	decreased grip strength	Ank3<em1(IMPC)Bay>/Ank3<+>	C57BL/6N-Ank3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471863	F	MP:0001399	hyperactivity	Ankrd50<em1(IMPC)Bay>/Ankrd50<em1(IMPC)Bay>	C57BL/6N-Ankrd50<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471863	F	MP:0011110	preweaning lethality, incomplete penetrance	Ankrd50<em1(IMPC)Bay>/Ankrd50<em1(IMPC)Bay>	C57BL/6N-Ankrd50<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471863	M	MP:0002574	increased vertical activity	Ankrd50<em1(IMPC)Bay>/Ankrd50<em1(IMPC)Bay>	C57BL/6N-Ankrd50<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471864	M	MP:0001513	limb grasping	Anks1<em1(IMPC)Bay>/Anks1<+>	C57BL/6N-Anks1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471866	F	MP:0000703	abnormal thymus morphology	Ano2<em1(IMPC)Ccpcz>/Ano2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ano2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471866	M	MP:0002339	abnormal lymph node morphology	Ano2<em1(IMPC)Ccpcz>/Ano2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ano2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471866	F	MP:0001364	decreased anxiety-related response	Ano2<em1(IMPC)Ccpcz>/Ano2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ano2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471866	F	MP:0000709	enlarged thymus	Ano2<em1(IMPC)Ccpcz>/Ano2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ano2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471866	M	MP:0000702	enlarged lymph nodes	Ano2<em1(IMPC)Ccpcz>/Ano2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ano2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471867	F	MP:0020421	increased freezing behavior	Anxa13<em1(IMPC)Kmpc>/Anxa13<em1(IMPC)Kmpc>	C57BL/6NTac-Anxa13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471867	M	MP:0002997	enlarged seminal vesicle	Anxa13<em1(IMPC)Kmpc>/Anxa13<em1(IMPC)Kmpc>	C57BL/6NTac-Anxa13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471867	M	MP:0001146	abnormal testis morphology	Anxa13<em1(IMPC)Kmpc>/Anxa13<em1(IMPC)Kmpc>	C57BL/6NTac-Anxa13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471868	F	MP:0010378	increased respiratory quotient	Aprt<em1(IMPC)Hmgu>/Aprt<+>	C57BL/6NCrl-Aprt<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471869	F	MP:0003795	abnormal bone structure	Arhgef28<tm1b(EUCOMM)Wtsi>/Arhgef28<tm1b(EUCOMM)Wtsi>	C57BL/6N-Arhgef28<tm1b(EUCOMM)Wtsi>/H	N	MGI:5576271
MGI:7471870	M	MP:0000274	enlarged heart	Arl16<em1(IMPC)Ccpcz>/Arl16<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arl16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471870	M	MP:0001262	decreased body weight	Arl16<em1(IMPC)Ccpcz>/Arl16<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arl16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471870	F	MP:0000703	abnormal thymus morphology	Arl16<em1(IMPC)Ccpcz>/Arl16<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arl16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471870	M	MP:0000759	abnormal skeletal muscle morphology	Arl16<em1(IMPC)Ccpcz>/Arl16<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arl16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471870	F	MP:0000709	enlarged thymus	Arl16<em1(IMPC)Ccpcz>/Arl16<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arl16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471870	M	MP:0001146	abnormal testis morphology	Arl16<em1(IMPC)Ccpcz>/Arl16<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arl16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471870	M	MP:0000692	small spleen	Arl16<em1(IMPC)Ccpcz>/Arl16<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arl16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471870	M	MP:0001147	small testis	Arl16<em1(IMPC)Ccpcz>/Arl16<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arl16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471870	M	MP:0002092	abnormal eye morphology	Arl16<em1(IMPC)Ccpcz>/Arl16<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arl16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471870	M	MP:0004083	polysyndactyly	Arl16<em1(IMPC)Ccpcz>/Arl16<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arl16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471870	M	MP:0000689	abnormal spleen morphology	Arl16<em1(IMPC)Ccpcz>/Arl16<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arl16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471870	M	MP:0000266	abnormal heart morphology	Arl16<em1(IMPC)Ccpcz>/Arl16<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arl16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471870	M	MP:0002110	abnormal digit morphology	Arl16<em1(IMPC)Ccpcz>/Arl16<em1(IMPC)Ccpcz>	C57BL/6NCrl-Arl16<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471871	F	MP:0003731	abnormal retina outer nuclear layer morphology	Arl6ip6<em1(IMPC)Bay>/Arl6ip6<em1(IMPC)Bay>	C57BL/6N-Arl6ip6<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471874	F	MP:0010506	prolonged RR interval	Asap1<em1(IMPC)Wtsi>/Asap1<em1(IMPC)Wtsi>	C57BL/6NCrl-Asap1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:7471874	F	MP:0005333	decreased heart rate	Asap1<em1(IMPC)Wtsi>/Asap1<em1(IMPC)Wtsi>	C57BL/6NCrl-Asap1<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:7471875	F	MP:0002060	abnormal skin morphology	Ascl5<em1(IMPC)Ccpcz>/Ascl5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ascl5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471875	F	MP:0000709	enlarged thymus	Ascl5<em1(IMPC)Ccpcz>/Ascl5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ascl5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471875	F	MP:0000703	abnormal thymus morphology	Ascl5<em1(IMPC)Ccpcz>/Ascl5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ascl5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471875	M	MP:0000274	enlarged heart	Ascl5<em1(IMPC)Ccpcz>/Ascl5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ascl5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471875	M	MP:0000266	abnormal heart morphology	Ascl5<em1(IMPC)Ccpcz>/Ascl5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ascl5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471875	M	MP:0010090	increased circulating creatine kinase level	Ascl5<em1(IMPC)Ccpcz>/Ascl5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ascl5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471876	F	MP:0000601	small liver	Asic3<em1(IMPC)Mbp>/Asic3<em1(IMPC)Mbp>	C57BL/6NCrl-Asic3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471876	F	MP:0009142	decreased prepulse inhibition	Asic3<em1(IMPC)Mbp>/Asic3<em1(IMPC)Mbp>	C57BL/6NCrl-Asic3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471876	F	MP:0001258	decreased body length	Asic3<em1(IMPC)Mbp>/Asic3<em1(IMPC)Mbp>	C57BL/6NCrl-Asic3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471876	F	MP:0000689	abnormal spleen morphology	Asic3<em1(IMPC)Mbp>/Asic3<em1(IMPC)Mbp>	C57BL/6NCrl-Asic3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471876	F	MP:0000598	abnormal liver morphology	Asic3<em1(IMPC)Mbp>/Asic3<em1(IMPC)Mbp>	C57BL/6NCrl-Asic3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471876	F	MP:0009342	enlarged gallbladder	Asic3<em1(IMPC)Mbp>/Asic3<em1(IMPC)Mbp>	C57BL/6NCrl-Asic3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471876	F	MP:0000691	enlarged spleen	Asic3<em1(IMPC)Mbp>/Asic3<em1(IMPC)Mbp>	C57BL/6NCrl-Asic3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471876	F	MP:0005084	abnormal gallbladder morphology	Asic3<em1(IMPC)Mbp>/Asic3<em1(IMPC)Mbp>	C57BL/6NCrl-Asic3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471877	F	MP:0000709	enlarged thymus	Asphd1<em1(IMPC)Ccpcz>/Asphd1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Asphd1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471877	F	MP:0002110	abnormal digit morphology	Asphd1<em1(IMPC)Ccpcz>/Asphd1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Asphd1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471877	F	MP:0002100	abnormal tooth morphology	Asphd1<em1(IMPC)Ccpcz>/Asphd1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Asphd1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471877	M	MP:0002092	abnormal eye morphology	Asphd1<em1(IMPC)Ccpcz>/Asphd1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Asphd1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471877	M	MP:0001297	microphthalmia	Asphd1<em1(IMPC)Ccpcz>/Asphd1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Asphd1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471877	M	MP:0002111	abnormal tail morphology	Asphd1<em1(IMPC)Ccpcz>/Asphd1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Asphd1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471877	F	MP:0000703	abnormal thymus morphology	Asphd1<em1(IMPC)Ccpcz>/Asphd1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Asphd1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471877	F	MP:0002966	decreased circulating alkaline phosphatase level	Asphd1<em1(IMPC)Ccpcz>/Asphd1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Asphd1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471879	M	MP:0000266	abnormal heart morphology	Ate1<em1(IMPC)Ccpcz>/Ate1<+>	C57BL/6NCrl-Ate1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471879	M	MP:0002059	abnormal seminal vesicle morphology	Ate1<em1(IMPC)Ccpcz>/Ate1<+>	C57BL/6NCrl-Ate1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471879	M	MP:0000274	enlarged heart	Ate1<em1(IMPC)Ccpcz>/Ate1<+>	C57BL/6NCrl-Ate1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471879	M	MP:0001944	abnormal pancreas morphology	Ate1<em1(IMPC)Ccpcz>/Ate1<+>	C57BL/6NCrl-Ate1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471881	M	MP:0006203	eye hemorrhage	Atp1b1<em1(IMPC)Mbp>/Atp1b1<+>	C57BL/6NCrl-Atp1b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471881	M	MP:0002060	abnormal skin morphology	Atp1b1<em1(IMPC)Mbp>/Atp1b1<+>	C57BL/6NCrl-Atp1b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471881	M	MP:0010393	shortened QRS complex duration	Atp1b1<em1(IMPC)Mbp>/Atp1b1<+>	C57BL/6NCrl-Atp1b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471881	M	MP:0001146	abnormal testis morphology	Atp1b1<em1(IMPC)Mbp>/Atp1b1<+>	C57BL/6NCrl-Atp1b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471881	F	MP:0001402	decreased locomotor activity	Atp1b1<em1(IMPC)Mbp>/Atp1b1<+>	C57BL/6NCrl-Atp1b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471881	F	MP:0002699	abnormal vitreous body morphology	Atp1b1<em1(IMPC)Mbp>/Atp1b1<+>	C57BL/6NCrl-Atp1b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471881	M	MP:0001148	enlarged testis	Atp1b1<em1(IMPC)Mbp>/Atp1b1<+>	C57BL/6NCrl-Atp1b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471881	F	MP:0001304	cataract	Atp1b1<em1(IMPC)Mbp>/Atp1b1<+>	C57BL/6NCrl-Atp1b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471881	M	MP:0001488	increased startle reflex	Atp1b1<em1(IMPC)Mbp>/Atp1b1<+>	C57BL/6NCrl-Atp1b1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471883	M	MP:0001925	male infertility	Atp2b4<em1(IMPC)Bay>/Atp2b4<em1(IMPC)Bay>	C57BL/6N-Atp2b4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471885	F	MP:0003795	abnormal bone structure	Atp8b4<em1(IMPC)Bay>/Atp8b4<em1(IMPC)Bay>	C57BL/6N-Atp8b4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471885	F	MP:0010123	increased bone mineral content	Atp8b4<em1(IMPC)Bay>/Atp8b4<em1(IMPC)Bay>	C57BL/6N-Atp8b4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471885	F	MP:0003961	decreased lean body mass	Atp8b4<em1(IMPC)Bay>/Atp8b4<em1(IMPC)Bay>	C57BL/6N-Atp8b4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471887	F	MP:0002092	abnormal eye morphology	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471887	F	MP:0009456	impaired cued conditioning behavior	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471887	F	MP:0000432	abnormal head morphology	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471887	M	MP:0000266	abnormal heart morphology	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471887	F	MP:0002989	small kidney	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471887	M	MP:0000274	enlarged heart	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471887	F	MP:0005011	increased eosinophil cell number	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471887	F	MP:0000709	enlarged thymus	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471887	F	MP:0005599	increased cardiac muscle contractility	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471887	F	MP:0002135	abnormal kidney morphology	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471887	M	MP:0020421	increased freezing behavior	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471887	F	MP:0001293	anophthalmia	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471887	F	MP:0009454	impaired contextual conditioning behavior	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471887	F	MP:0000703	abnormal thymus morphology	Babam1<em1(IMPC)Ccpcz>/Babam1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Babam1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471888	M	MP:0001510	abnormal coat appearance	Banf1<em1(IMPC)J>/Banf1<+>	C57BL/6NJ-Banf1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7471888	M	MP:0000367	abnormal coat/ hair morphology	Banf1<em1(IMPC)J>/Banf1<+>	C57BL/6NJ-Banf1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7471889	M	MP:0000266	abnormal heart morphology	Bbs12<em1(IMPC)Ccpcz>/Bbs12<+>	C57BL/6NCrl-Bbs12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471889	F	MP:0000709	enlarged thymus	Bbs12<em1(IMPC)Ccpcz>/Bbs12<+>	C57BL/6NCrl-Bbs12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471889	M	MP:0000274	enlarged heart	Bbs12<em1(IMPC)Ccpcz>/Bbs12<+>	C57BL/6NCrl-Bbs12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471889	F	MP:0000703	abnormal thymus morphology	Bbs12<em1(IMPC)Ccpcz>/Bbs12<+>	C57BL/6NCrl-Bbs12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471889	F	MP:0000691	enlarged spleen	Bbs12<em1(IMPC)Ccpcz>/Bbs12<+>	C57BL/6NCrl-Bbs12<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471892	F	MP:0011100	preweaning lethality, complete penetrance	Bcl9<em1(IMPC)Bay>/Bcl9<em1(IMPC)Bay>	C57BL/6N-Bcl9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471893	F	MP:0002966	decreased circulating alkaline phosphatase level	Blcap<em1(IMPC)J>/Blcap<em1(IMPC)J>	C57BL/6NJ-Blcap<em1(IMPC)J>/J	N	MGI:5576271
MGI:7471893	F	MP:0013279	increased fasting circulating glucose level	Blcap<em1(IMPC)J>/Blcap<em1(IMPC)J>	C57BL/6NJ-Blcap<em1(IMPC)J>/J	N	MGI:5576271
MGI:7471894	M	MP:0000220	increased monocyte cell number	Bloc1s5<em1(IMPC)Tcp>/Bloc1s5<+>	C57BL/6NCrl-Bloc1s5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7471895	F	MP:0003795	abnormal bone structure	Bmpr1b<em1(IMPC)Mbp>/Bmpr1b<em1(IMPC)Mbp>	C57BL/6NCrl-Bmpr1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471895	F	MP:0000601	small liver	Bmpr1b<em1(IMPC)Mbp>/Bmpr1b<em1(IMPC)Mbp>	C57BL/6NCrl-Bmpr1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471895	M	MP:0001147	small testis	Bmpr1b<em1(IMPC)Mbp>/Bmpr1b<em1(IMPC)Mbp>	C57BL/6NCrl-Bmpr1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471895	M	MP:0001319	irregularly shaped pupil	Bmpr1b<em1(IMPC)Mbp>/Bmpr1b<em1(IMPC)Mbp>	C57BL/6NCrl-Bmpr1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471895	M	MP:0020421	increased freezing behavior	Bmpr1b<em1(IMPC)Mbp>/Bmpr1b<em1(IMPC)Mbp>	C57BL/6NCrl-Bmpr1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471895	M	MP:0001157	small seminal vesicle	Bmpr1b<em1(IMPC)Mbp>/Bmpr1b<em1(IMPC)Mbp>	C57BL/6NCrl-Bmpr1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471895	F	MP:0000598	abnormal liver morphology	Bmpr1b<em1(IMPC)Mbp>/Bmpr1b<em1(IMPC)Mbp>	C57BL/6NCrl-Bmpr1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471895	F	MP:0001926	female infertility	Bmpr1b<em1(IMPC)Mbp>/Bmpr1b<em1(IMPC)Mbp>	C57BL/6NCrl-Bmpr1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471895	M	MP:0002059	abnormal seminal vesicle morphology	Bmpr1b<em1(IMPC)Mbp>/Bmpr1b<em1(IMPC)Mbp>	C57BL/6NCrl-Bmpr1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471895	M	MP:0001146	abnormal testis morphology	Bmpr1b<em1(IMPC)Mbp>/Bmpr1b<em1(IMPC)Mbp>	C57BL/6NCrl-Bmpr1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471898	F	MP:0004258	abnormal placenta size	Brat1<em1(IMPC)Bay>/Brat1<em1(IMPC)Bay>	C57BL/6N-Brat1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471899	M	MP:0001262	decreased body weight	Brinp3<em1(IMPC)Ccpcz>/Brinp3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Brinp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471899	F	MP:0000538	abnormal urinary bladder morphology	Brinp3<em1(IMPC)Ccpcz>/Brinp3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Brinp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471899	F	MP:0000274	enlarged heart	Brinp3<em1(IMPC)Ccpcz>/Brinp3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Brinp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471899	F	MP:0000266	abnormal heart morphology	Brinp3<em1(IMPC)Ccpcz>/Brinp3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Brinp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471899	M	MP:0004924	abnormal behavior	Brinp3<em1(IMPC)Ccpcz>/Brinp3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Brinp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471899	F	MP:0002135	abnormal kidney morphology	Brinp3<em1(IMPC)Ccpcz>/Brinp3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Brinp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471901	M	MP:0000223	decreased monocyte cell number	C1ql3<em1(IMPC)H>/C1ql3<em1(IMPC)H>	C57BL/6NTac-C1ql3<em1(IMPC)H>/H	N	MGI:5576271
MGI:7471901	M	MP:0000221	decreased leukocyte cell number	C1ql3<em1(IMPC)H>/C1ql3<em1(IMPC)H>	C57BL/6NTac-C1ql3<em1(IMPC)H>/H	N	MGI:5576271
MGI:7471901	M	MP:0000222	decreased neutrophil cell number	C1ql3<em1(IMPC)H>/C1ql3<em1(IMPC)H>	C57BL/6NTac-C1ql3<em1(IMPC)H>/H	N	MGI:5576271
MGI:7471901	M	MP:0005016	decreased lymphocyte cell number	C1ql3<em1(IMPC)H>/C1ql3<em1(IMPC)H>	C57BL/6NTac-C1ql3<em1(IMPC)H>/H	N	MGI:5576271
MGI:7471902	M	MP:0000274	enlarged heart	Cabin1<em1(IMPC)Ccpcz>/Cabin1<+>	C57BL/6NCrl-Cabin1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471902	M	MP:0000266	abnormal heart morphology	Cabin1<em1(IMPC)Ccpcz>/Cabin1<+>	C57BL/6NCrl-Cabin1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471902	F	MP:0000703	abnormal thymus morphology	Cabin1<em1(IMPC)Ccpcz>/Cabin1<+>	C57BL/6NCrl-Cabin1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471902	F	MP:0000709	enlarged thymus	Cabin1<em1(IMPC)Ccpcz>/Cabin1<+>	C57BL/6NCrl-Cabin1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471904	M	MP:0020421	increased freezing behavior	Cacna1a<em1(IMPC)H>/Cacna1a<+>	C57BL/6NTac-Cacna1a<em1(IMPC)H>/H	N	MGI:5576271
MGI:7471906	M	MP:0002059	abnormal seminal vesicle morphology	Cactin<em1(IMPC)Ccpcz>/Cactin<+>	C57BL/6NCrl-Cactin<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471906	M	MP:0001147	small testis	Cactin<em1(IMPC)Ccpcz>/Cactin<+>	C57BL/6NCrl-Cactin<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471906	F	MP:0000709	enlarged thymus	Cactin<em1(IMPC)Ccpcz>/Cactin<+>	C57BL/6NCrl-Cactin<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471906	M	MP:0000266	abnormal heart morphology	Cactin<em1(IMPC)Ccpcz>/Cactin<+>	C57BL/6NCrl-Cactin<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471906	F	MP:0000703	abnormal thymus morphology	Cactin<em1(IMPC)Ccpcz>/Cactin<+>	C57BL/6NCrl-Cactin<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471906	M	MP:0001146	abnormal testis morphology	Cactin<em1(IMPC)Ccpcz>/Cactin<+>	C57BL/6NCrl-Cactin<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471906	M	MP:0002997	enlarged seminal vesicle	Cactin<em1(IMPC)Ccpcz>/Cactin<+>	C57BL/6NCrl-Cactin<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471906	M	MP:0000274	enlarged heart	Cactin<em1(IMPC)Ccpcz>/Cactin<+>	C57BL/6NCrl-Cactin<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471908	M	MP:0011110	preweaning lethality, incomplete penetrance	Cacybp<tm1b(EUCOMM)Wtsi>/Cacybp<tm1b(EUCOMM)Wtsi>	C57BL/6N-Cacybp<tm1b(EUCOMM)Wtsi>/Tcp	N	MGI:5576271
MGI:7471909	M	MP:0000692	small spleen	Calb1<em1(IMPC)Ccpcz>/Calb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Calb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471909	M	MP:0000689	abnormal spleen morphology	Calb1<em1(IMPC)Ccpcz>/Calb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Calb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471909	F	MP:0009709	hydrometra	Calb1<em1(IMPC)Ccpcz>/Calb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Calb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471909	F	MP:0005599	increased cardiac muscle contractility	Calb1<em1(IMPC)Ccpcz>/Calb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Calb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471909	M	MP:0001146	abnormal testis morphology	Calb1<em1(IMPC)Ccpcz>/Calb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Calb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471909	M	MP:0001325	abnormal retina morphology	Calb1<em1(IMPC)Ccpcz>/Calb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Calb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471909	F	MP:0000160	kyphosis	Calb1<em1(IMPC)Ccpcz>/Calb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Calb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471909	M	MP:0000691	enlarged spleen	Calb1<em1(IMPC)Ccpcz>/Calb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Calb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471909	F	MP:0004174	abnormal spine curvature	Calb1<em1(IMPC)Ccpcz>/Calb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Calb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471909	F	MP:0001120	abnormal uterus morphology	Calb1<em1(IMPC)Ccpcz>/Calb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Calb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471909	M	MP:0001147	small testis	Calb1<em1(IMPC)Ccpcz>/Calb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Calb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471909	F	MP:0003921	abnormal heart left ventricle morphology	Calb1<em1(IMPC)Ccpcz>/Calb1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Calb1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471910	F	MP:0000709	enlarged thymus	Canx<em1(IMPC)Ccpcz>/Canx<+>	C57BL/6NCrl-Canx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471910	F	MP:0000691	enlarged spleen	Canx<em1(IMPC)Ccpcz>/Canx<+>	C57BL/6NCrl-Canx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471910	F	MP:0004906	enlarged uterus	Canx<em1(IMPC)Ccpcz>/Canx<+>	C57BL/6NCrl-Canx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471910	F	MP:0001120	abnormal uterus morphology	Canx<em1(IMPC)Ccpcz>/Canx<+>	C57BL/6NCrl-Canx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471910	F	MP:0000703	abnormal thymus morphology	Canx<em1(IMPC)Ccpcz>/Canx<+>	C57BL/6NCrl-Canx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471910	M	MP:0000274	enlarged heart	Canx<em1(IMPC)Ccpcz>/Canx<+>	C57BL/6NCrl-Canx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471910	F	MP:0000689	abnormal spleen morphology	Canx<em1(IMPC)Ccpcz>/Canx<+>	C57BL/6NCrl-Canx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471910	M	MP:0000266	abnormal heart morphology	Canx<em1(IMPC)Ccpcz>/Canx<+>	C57BL/6NCrl-Canx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471911	M	MP:0000709	enlarged thymus	Canx<em1(IMPC)Ccpcz>/Canx<em1(IMPC)Ccpcz>	C57BL/6NCrl-Canx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471911	M	MP:0000759	abnormal skeletal muscle morphology	Canx<em1(IMPC)Ccpcz>/Canx<em1(IMPC)Ccpcz>	C57BL/6NCrl-Canx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471911	M	MP:0000703	abnormal thymus morphology	Canx<em1(IMPC)Ccpcz>/Canx<em1(IMPC)Ccpcz>	C57BL/6NCrl-Canx<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471913	M	MP:0000702	enlarged lymph nodes	Car6<em1(IMPC)Ccpcz>/Car6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Car6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471913	M	MP:0001147	small testis	Car6<em1(IMPC)Ccpcz>/Car6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Car6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471913	F	MP:0000703	abnormal thymus morphology	Car6<em1(IMPC)Ccpcz>/Car6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Car6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471913	M	MP:0013129	abnormal tooth color	Car6<em1(IMPC)Ccpcz>/Car6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Car6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471913	M	MP:0005011	increased eosinophil cell number	Car6<em1(IMPC)Ccpcz>/Car6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Car6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471913	M	MP:0001146	abnormal testis morphology	Car6<em1(IMPC)Ccpcz>/Car6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Car6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471913	F	MP:0000689	abnormal spleen morphology	Car6<em1(IMPC)Ccpcz>/Car6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Car6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471913	F	MP:0000691	enlarged spleen	Car6<em1(IMPC)Ccpcz>/Car6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Car6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471913	F	MP:0000709	enlarged thymus	Car6<em1(IMPC)Ccpcz>/Car6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Car6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471913	M	MP:0002339	abnormal lymph node morphology	Car6<em1(IMPC)Ccpcz>/Car6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Car6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471914	M	MP:0001914	hemorrhage	Cars2<em1(IMPC)Bay>/Cars2<+>	C57BL/6N-Cars2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471915	M	MP:0002941	increased circulating alanine transaminase level	Cav2<em1(IMPC)Kmpc>/Cav2<em1(IMPC)Kmpc>	C57BL/6NTac-Cav2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471915	F	MP:0002092	abnormal eye morphology	Cav2<em1(IMPC)Kmpc>/Cav2<em1(IMPC)Kmpc>	C57BL/6NTac-Cav2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471915	M	MP:0005568	increased circulating total protein level	Cav2<em1(IMPC)Kmpc>/Cav2<em1(IMPC)Kmpc>	C57BL/6NTac-Cav2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471916	M	MP:0002059	abnormal seminal vesicle morphology	Cav3<em1(IMPC)Kmpc>/Cav3<em1(IMPC)Kmpc>	C57BL/6NTac-Cav3<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471916	M	MP:0011877	absent liver	Cav3<em1(IMPC)Kmpc>/Cav3<em1(IMPC)Kmpc>	C57BL/6NTac-Cav3<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471916	F	MP:0001126	abnormal ovary morphology	Cav3<em1(IMPC)Kmpc>/Cav3<em1(IMPC)Kmpc>	C57BL/6NTac-Cav3<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471919	M	MP:0002060	abnormal skin morphology	Ccdc183<em1(IMPC)Hmgu>/Ccdc183<em1(IMPC)Hmgu>	C57BL/6NCrl-Ccdc183<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471921	F	MP:0000428	abnormal craniofacial morphology	Ccdc186<em1(IMPC)Mbp>/Ccdc186<em1(IMPC)Mbp>	C57BL/6NCrl-Ccdc186<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471921	F	MP:0001785	edema	Ccdc186<em1(IMPC)Mbp>/Ccdc186<em1(IMPC)Mbp>	C57BL/6NCrl-Ccdc186<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471921	F	MP:0003984	embryonic growth retardation	Ccdc186<em1(IMPC)Mbp>/Ccdc186<em1(IMPC)Mbp>	C57BL/6NCrl-Ccdc186<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471925	F	MP:0008806	increased circulating amylase level	Cd1d1<em1(IMPC)H>/Cd1d1<em1(IMPC)H>	C57BL/6NTac-Cd1d1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7471925	M	MP:0010068	decreased red blood cell distribution width	Cd1d1<em1(IMPC)H>/Cd1d1<em1(IMPC)H>	C57BL/6NTac-Cd1d1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7471926	M	MP:0001146	abnormal testis morphology	Cd27<em1(IMPC)Ccpcz>/Cd27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471926	M	MP:0000266	abnormal heart morphology	Cd27<em1(IMPC)Ccpcz>/Cd27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471926	M	MP:0001157	small seminal vesicle	Cd27<em1(IMPC)Ccpcz>/Cd27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471926	M	MP:0002059	abnormal seminal vesicle morphology	Cd27<em1(IMPC)Ccpcz>/Cd27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471926	M	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	Cd27<em1(IMPC)Ccpcz>/Cd27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471926	F	MP:0000689	abnormal spleen morphology	Cd27<em1(IMPC)Ccpcz>/Cd27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471926	M	MP:0000274	enlarged heart	Cd27<em1(IMPC)Ccpcz>/Cd27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471926	M	MP:0001147	small testis	Cd27<em1(IMPC)Ccpcz>/Cd27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471926	M	MP:0003961	decreased lean body mass	Cd27<em1(IMPC)Ccpcz>/Cd27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471927	M	MP:0010379	decreased respiratory quotient	Cdkl5<tm1dIcs>/Y	C57BL/6N-Cdkl5<tm1dIcs>/Ics	N	MGI:5576271
MGI:7471928	M	MP:0001402	decreased locomotor activity	Cenpv<em1(IMPC)Hmgu>/Cenpv<em1(IMPC)Hmgu>	C57BL/6NCrl-Cenpv<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471929	F	MP:0000689	abnormal spleen morphology	Cer1<em1(IMPC)Ccpcz>/Cer1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cer1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471929	M	MP:0000274	enlarged heart	Cer1<em1(IMPC)Ccpcz>/Cer1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cer1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471929	F	MP:0000691	enlarged spleen	Cer1<em1(IMPC)Ccpcz>/Cer1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cer1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471929	F	MP:0003036	vertebral transformation	Cer1<em1(IMPC)Ccpcz>/Cer1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cer1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471929	M	MP:0001146	abnormal testis morphology	Cer1<em1(IMPC)Ccpcz>/Cer1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cer1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471929	M	MP:0000266	abnormal heart morphology	Cer1<em1(IMPC)Ccpcz>/Cer1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cer1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471929	M	MP:0001147	small testis	Cer1<em1(IMPC)Ccpcz>/Cer1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cer1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471931	M	MP:0003961	decreased lean body mass	Ces5a<em1(IMPC)J>/Ces5a<em1(IMPC)J>	C57BL/6NJ-Ces5a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7471931	M	MP:0010024	increased total body fat amount	Ces5a<em1(IMPC)J>/Ces5a<em1(IMPC)J>	C57BL/6NJ-Ces5a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7471931	M	MP:0010124	decreased bone mineral content	Ces5a<em1(IMPC)J>/Ces5a<em1(IMPC)J>	C57BL/6NJ-Ces5a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7471931	M	MP:0000063	decreased bone mineral density	Ces5a<em1(IMPC)J>/Ces5a<em1(IMPC)J>	C57BL/6NJ-Ces5a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7471932	F	MP:0003795	abnormal bone structure	Cfap300<em1(IMPC)Bay>/Cfap300<+>	C57BL/6N-Cfap300<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471933	M	MP:0002768	small adrenal glands	Cfd<em1(IMPC)Mbp>/Cfd<em1(IMPC)Mbp>	C57BL/6NCrl-Cfd<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471933	F	MP:0002135	abnormal kidney morphology	Cfd<em1(IMPC)Mbp>/Cfd<em1(IMPC)Mbp>	C57BL/6NCrl-Cfd<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471933	M	MP:0000639	abnormal adrenal gland morphology	Cfd<em1(IMPC)Mbp>/Cfd<em1(IMPC)Mbp>	C57BL/6NCrl-Cfd<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471933	F	MP:0002989	small kidney	Cfd<em1(IMPC)Mbp>/Cfd<em1(IMPC)Mbp>	C57BL/6NCrl-Cfd<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471937	F	MP:0001404	no spontaneous movement	Chmp2b<em1(IMPC)Mbp>/Chmp2b<em1(IMPC)Mbp>	C57BL/6NCrl-Chmp2b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471938	F	MP:0002135	abnormal kidney morphology	Chrna2<em1(IMPC)Mbp>/Chrna2<em1(IMPC)Mbp>	C57BL/6NCrl-Chrna2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471938	F	MP:0002989	small kidney	Chrna2<em1(IMPC)Mbp>/Chrna2<em1(IMPC)Mbp>	C57BL/6NCrl-Chrna2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471938	M	MP:0001200	thick skin	Chrna2<em1(IMPC)Mbp>/Chrna2<em1(IMPC)Mbp>	C57BL/6NCrl-Chrna2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471938	M	MP:0002060	abnormal skin morphology	Chrna2<em1(IMPC)Mbp>/Chrna2<em1(IMPC)Mbp>	C57BL/6NCrl-Chrna2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471940	F	MP:0001258	decreased body length	Clec5a<em1(IMPC)Mbp>/Clec5a<em1(IMPC)Mbp>	C57BL/6NCrl-Clec5a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471940	F	MP:0000709	enlarged thymus	Clec5a<em1(IMPC)Mbp>/Clec5a<em1(IMPC)Mbp>	C57BL/6NCrl-Clec5a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471940	F	MP:0006203	eye hemorrhage	Clec5a<em1(IMPC)Mbp>/Clec5a<em1(IMPC)Mbp>	C57BL/6NCrl-Clec5a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471940	M	MP:0001289	persistence of hyaloid vascular system	Clec5a<em1(IMPC)Mbp>/Clec5a<em1(IMPC)Mbp>	C57BL/6NCrl-Clec5a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471940	F	MP:0000703	abnormal thymus morphology	Clec5a<em1(IMPC)Mbp>/Clec5a<em1(IMPC)Mbp>	C57BL/6NCrl-Clec5a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471940	F	MP:0001314	cornea opacity	Clec5a<em1(IMPC)Mbp>/Clec5a<em1(IMPC)Mbp>	C57BL/6NCrl-Clec5a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471941	M	MP:0005011	increased eosinophil cell number	Clock<em1(IMPC)Ccpcz>/Clock<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clock<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471941	M	MP:0010068	decreased red blood cell distribution width	Clock<em1(IMPC)Ccpcz>/Clock<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clock<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471941	F	MP:0000703	abnormal thymus morphology	Clock<em1(IMPC)Ccpcz>/Clock<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clock<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471941	M	MP:0001556	increased circulating HDL cholesterol level	Clock<em1(IMPC)Ccpcz>/Clock<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clock<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471941	M	MP:0010896	decreased lung compliance	Clock<em1(IMPC)Ccpcz>/Clock<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clock<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471941	F	MP:0005333	decreased heart rate	Clock<em1(IMPC)Ccpcz>/Clock<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clock<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471941	F	MP:0000709	enlarged thymus	Clock<em1(IMPC)Ccpcz>/Clock<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clock<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471941	M	MP:0001552	increased circulating triglyceride level	Clock<em1(IMPC)Ccpcz>/Clock<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clock<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471941	M	MP:0002100	abnormal tooth morphology	Clock<em1(IMPC)Ccpcz>/Clock<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clock<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471941	M	MP:0011044	increased lung elastance	Clock<em1(IMPC)Ccpcz>/Clock<em1(IMPC)Ccpcz>	C57BL/6NCrl-Clock<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471942	M	MP:0000274	enlarged heart	Cngb3<em1(IMPC)Ccpcz>/Cngb3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cngb3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471942	F	MP:0000709	enlarged thymus	Cngb3<em1(IMPC)Ccpcz>/Cngb3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cngb3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471942	M	MP:0000689	abnormal spleen morphology	Cngb3<em1(IMPC)Ccpcz>/Cngb3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cngb3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471942	M	MP:0000691	enlarged spleen	Cngb3<em1(IMPC)Ccpcz>/Cngb3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cngb3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471942	F	MP:0000703	abnormal thymus morphology	Cngb3<em1(IMPC)Ccpcz>/Cngb3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cngb3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471942	M	MP:0000266	abnormal heart morphology	Cngb3<em1(IMPC)Ccpcz>/Cngb3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cngb3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471942	M	MP:0001146	abnormal testis morphology	Cngb3<em1(IMPC)Ccpcz>/Cngb3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cngb3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471942	F	MP:0000702	enlarged lymph nodes	Cngb3<em1(IMPC)Ccpcz>/Cngb3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cngb3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471942	F	MP:0002339	abnormal lymph node morphology	Cngb3<em1(IMPC)Ccpcz>/Cngb3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cngb3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471942	M	MP:0001147	small testis	Cngb3<em1(IMPC)Ccpcz>/Cngb3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cngb3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471943	F	MP:0001120	abnormal uterus morphology	Cnot3<em1(IMPC)Rbrc>/Cnot3<+>	C57BL/6NJcl-Cnot3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7471943	M	MP:0005344	increased circulating bilirubin level	Cnot3<em1(IMPC)Rbrc>/Cnot3<+>	C57BL/6NJcl-Cnot3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7471943	M	MP:0002644	decreased circulating triglyceride level	Cnot3<em1(IMPC)Rbrc>/Cnot3<+>	C57BL/6NJcl-Cnot3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7471943	F	MP:0004924	abnormal behavior	Cnot3<em1(IMPC)Rbrc>/Cnot3<+>	C57BL/6NJcl-Cnot3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7471943	F	MP:0002797	increased thigmotaxis	Cnot3<em1(IMPC)Rbrc>/Cnot3<+>	C57BL/6NJcl-Cnot3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7471943	F	MP:0001399	hyperactivity	Cnot3<em1(IMPC)Rbrc>/Cnot3<+>	C57BL/6NJcl-Cnot3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7471943	F	MP:0010124	decreased bone mineral content	Cnot3<em1(IMPC)Rbrc>/Cnot3<+>	C57BL/6NJcl-Cnot3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7471943	F	MP:0000063	decreased bone mineral density	Cnot3<em1(IMPC)Rbrc>/Cnot3<+>	C57BL/6NJcl-Cnot3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7471943	F	MP:0009709	hydrometra	Cnot3<em1(IMPC)Rbrc>/Cnot3<+>	C57BL/6NJcl-Cnot3<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7471944	F	MP:0002152	abnormal brain morphology	Cnpy4<em1(IMPC)Ccpcz>/Cnpy4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cnpy4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471944	F	MP:0001891	hydrocephaly	Cnpy4<em1(IMPC)Ccpcz>/Cnpy4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cnpy4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471946	F	MP:0001120	abnormal uterus morphology	Cobll1<em1(IMPC)Ccpcz>/Cobll1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cobll1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471946	M	MP:0001529	abnormal vocalization	Cobll1<em1(IMPC)Ccpcz>/Cobll1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cobll1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471946	F	MP:0000703	abnormal thymus morphology	Cobll1<em1(IMPC)Ccpcz>/Cobll1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cobll1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471946	F	MP:0000689	abnormal spleen morphology	Cobll1<em1(IMPC)Ccpcz>/Cobll1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cobll1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471946	F	MP:0001126	abnormal ovary morphology	Cobll1<em1(IMPC)Ccpcz>/Cobll1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cobll1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471946	F	MP:0000691	enlarged spleen	Cobll1<em1(IMPC)Ccpcz>/Cobll1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cobll1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471946	F	MP:0003960	increased lean body mass	Cobll1<em1(IMPC)Ccpcz>/Cobll1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cobll1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471946	F	MP:0000709	enlarged thymus	Cobll1<em1(IMPC)Ccpcz>/Cobll1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cobll1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471947	M	MP:0020422	decreased freezing behavior	Cog5<em1(IMPC)Ccpcz>/Cog5<+>	C57BL/6NCrl-Cog5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471949	F	MP:0005635	decreased circulating bilirubin level	Cog8<em1(IMPC)J>/Cog8<+>	C57BL/6NJ-Cog8<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7471952	M	MP:0002075	abnormal coat/hair pigmentation	Crot<em1(IMPC)Kmpc>/Crot<em1(IMPC)Kmpc>	C57BL/6NTac-Crot<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471953	F	MP:0001399	hyperactivity	Cryzl1<em1(IMPC)Bay>/Cryzl1<em1(IMPC)Bay>	C57BL/6N-Cryzl1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471954	F	MP:0005012	decreased eosinophil cell number	Csf3<em1(IMPC)H>/Csf3<em1(IMPC)H>	C57BL/6NTac-Csf3<em1(IMPC)H>/H	N	MGI:5576271
MGI:7471954	M	MP:0002608	increased hematocrit	Csf3<em1(IMPC)H>/Csf3<em1(IMPC)H>	C57BL/6NTac-Csf3<em1(IMPC)H>/H	N	MGI:5576271
MGI:7471955	F	MP:0001325	abnormal retina morphology	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471955	M	MP:0000692	small spleen	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471955	F	MP:0005419	decreased circulating serum albumin level	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471955	F	MP:0009709	hydrometra	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471955	M	MP:0004357	long tibia	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471955	F	MP:0010090	increased circulating creatine kinase level	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471955	M	MP:0000274	enlarged heart	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471955	M	MP:0000266	abnormal heart morphology	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471955	F	MP:0000150	abnormal rib morphology	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471955	F	MP:0000154	rib fusion	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471955	F	MP:0001120	abnormal uterus morphology	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471955	F	MP:0000691	enlarged spleen	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471955	F	MP:0002110	abnormal digit morphology	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471955	F	MP:0002060	abnormal skin morphology	Cst6<em1(IMPC)Ccpcz>/Cst6<+>	C57BL/6NCrl-Cst6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471957	F	MP:0005278	abnormal cholesterol homeostasis	Cstf1<em1(IMPC)J>/Cstf1<+>	C57BL/6NJ-Cstf1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7471958	F	MP:0001258	decreased body length	Ctbp1<em1(IMPC)Bay>/Ctbp1<+>	C57BL/6N-Ctbp1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471960	F	MP:0002989	small kidney	Cthrc1<em1(IMPC)Mbp>/Cthrc1<em1(IMPC)Mbp>	C57BL/6NCrl-Cthrc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471960	F	MP:0000601	small liver	Cthrc1<em1(IMPC)Mbp>/Cthrc1<em1(IMPC)Mbp>	C57BL/6NCrl-Cthrc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471960	M	MP:0001289	persistence of hyaloid vascular system	Cthrc1<em1(IMPC)Mbp>/Cthrc1<em1(IMPC)Mbp>	C57BL/6NCrl-Cthrc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471960	M	MP:0001147	small testis	Cthrc1<em1(IMPC)Mbp>/Cthrc1<em1(IMPC)Mbp>	C57BL/6NCrl-Cthrc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471960	F	MP:0000598	abnormal liver morphology	Cthrc1<em1(IMPC)Mbp>/Cthrc1<em1(IMPC)Mbp>	C57BL/6NCrl-Cthrc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471960	F	MP:0002699	abnormal vitreous body morphology	Cthrc1<em1(IMPC)Mbp>/Cthrc1<em1(IMPC)Mbp>	C57BL/6NCrl-Cthrc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471960	M	MP:0001146	abnormal testis morphology	Cthrc1<em1(IMPC)Mbp>/Cthrc1<em1(IMPC)Mbp>	C57BL/6NCrl-Cthrc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471960	F	MP:0002135	abnormal kidney morphology	Cthrc1<em1(IMPC)Mbp>/Cthrc1<em1(IMPC)Mbp>	C57BL/6NCrl-Cthrc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471961	M	MP:0002599	increased mean platelet volume	Ctsz<em1(IMPC)H>/Ctsz<em1(IMPC)H>	C57BL/6NTac-Ctsz<em1(IMPC)H>/H	N	MGI:5576271
MGI:7471962	M	MP:0005419	decreased circulating serum albumin level	Cxcl14<em1(IMPC)H>/Cxcl14<em1(IMPC)H>	C57BL/6NTac-Cxcl14<em1(IMPC)H>/H	N	MGI:5576271
MGI:7471963	M	MP:0001489	decreased startle reflex	Cxcl5<em1(IMPC)Kmpc>/Cxcl5<em1(IMPC)Kmpc>	C57BL/6NTac-Cxcl5<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471965	M	MP:0002059	abnormal seminal vesicle morphology	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	M	MP:0000266	abnormal heart morphology	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	M	MP:0000274	enlarged heart	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	F	MP:0000702	enlarged lymph nodes	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	M	MP:0001157	small seminal vesicle	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	F	MP:0001293	anophthalmia	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	M	MP:0000538	abnormal urinary bladder morphology	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	M	MP:0000691	enlarged spleen	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	M	MP:0000692	small spleen	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	M	MP:0002217	small lymph nodes	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	M	MP:0000689	abnormal spleen morphology	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	F	MP:0002092	abnormal eye morphology	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	F	MP:0005011	increased eosinophil cell number	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	M	MP:0011874	enlarged urinary bladder	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471965	M	MP:0002135	abnormal kidney morphology	Dach2<em1(IMPC)Ccpcz>/Dach2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dach2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471966	M	MP:0003960	increased lean body mass	Dazap1<em1(IMPC)Ccpcz>/Dazap1<+>	C57BL/6NCrl-Dazap1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471966	M	MP:0000266	abnormal heart morphology	Dazap1<em1(IMPC)Ccpcz>/Dazap1<+>	C57BL/6NCrl-Dazap1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471966	M	MP:0000274	enlarged heart	Dazap1<em1(IMPC)Ccpcz>/Dazap1<+>	C57BL/6NCrl-Dazap1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471966	M	MP:0010025	decreased total body fat amount	Dazap1<em1(IMPC)Ccpcz>/Dazap1<+>	C57BL/6NCrl-Dazap1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471968	M	MP:0010123	increased bone mineral content	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:7471968	M	MP:0010025	decreased total body fat amount	Dbn1<tm1b(KOMP)Wtsi>/Dbn1<+>	C57BL/6N-Dbn1<tm1b(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:7471975	M	MP:0000219	increased neutrophil cell number	Dlgap2<em1(IMPC)Mhzh>/Dlgap2<em1(IMPC)Mhzh>	C57BL/6N-Dlgap2<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7471975	M	MP:0005016	decreased lymphocyte cell number	Dlgap2<em1(IMPC)Mhzh>/Dlgap2<em1(IMPC)Mhzh>	C57BL/6N-Dlgap2<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7471975	M	MP:0005011	increased eosinophil cell number	Dlgap2<em1(IMPC)Mhzh>/Dlgap2<em1(IMPC)Mhzh>	C57BL/6N-Dlgap2<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7471975	F	MP:0013279	increased fasting circulating glucose level	Dlgap2<em1(IMPC)Mhzh>/Dlgap2<em1(IMPC)Mhzh>	C57BL/6N-Dlgap2<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7471976	M	MP:0001399	hyperactivity	Dmwd<em1(IMPC)J>/Dmwd<em1(IMPC)J>	C57BL/6NJ-Dmwd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7471976	F	MP:0013279	increased fasting circulating glucose level	Dmwd<em1(IMPC)J>/Dmwd<em1(IMPC)J>	C57BL/6NJ-Dmwd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7471976	M	MP:0010052	increased grip strength	Dmwd<em1(IMPC)J>/Dmwd<em1(IMPC)J>	C57BL/6NJ-Dmwd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7471978	F	MP:0002590	increased mean corpuscular volume	Dnai4<em1(IMPC)J>/Dnai4<em1(IMPC)J>	C57BL/6NJ-Dnai4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7471978	M	MP:0001925	male infertility	Dnai4<em1(IMPC)J>/Dnai4<em1(IMPC)J>	C57BL/6NJ-Dnai4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7471979	F	MP:0003960	increased lean body mass	Edem1<em1(IMPC)Kmpc>/Edem1<em1(IMPC)Kmpc>	C57BL/6NTac-Edem1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471979	F	MP:0010123	increased bone mineral content	Edem1<em1(IMPC)Kmpc>/Edem1<em1(IMPC)Kmpc>	C57BL/6NTac-Edem1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471979	M	MP:0001556	increased circulating HDL cholesterol level	Edem1<em1(IMPC)Kmpc>/Edem1<em1(IMPC)Kmpc>	C57BL/6NTac-Edem1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471979	F	MP:0010025	decreased total body fat amount	Edem1<em1(IMPC)Kmpc>/Edem1<em1(IMPC)Kmpc>	C57BL/6NTac-Edem1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471980	M	MP:0000219	increased neutrophil cell number	Eef1d<em1(IMPC)Mbp>/Eef1d<+>	C57BL/6NCrl-Eef1d<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471980	F	MP:0002060	abnormal skin morphology	Eef1d<em1(IMPC)Mbp>/Eef1d<+>	C57BL/6NCrl-Eef1d<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471980	F	MP:0002699	abnormal vitreous body morphology	Eef1d<em1(IMPC)Mbp>/Eef1d<+>	C57BL/6NCrl-Eef1d<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471980	F	MP:0002092	abnormal eye morphology	Eef1d<em1(IMPC)Mbp>/Eef1d<+>	C57BL/6NCrl-Eef1d<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471980	F	MP:0001297	microphthalmia	Eef1d<em1(IMPC)Mbp>/Eef1d<+>	C57BL/6NCrl-Eef1d<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471981	F	MP:0003984	embryonic growth retardation	Eef1d<em1(IMPC)Mbp>/Eef1d<em1(IMPC)Mbp>	C57BL/6NCrl-Eef1d<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7471982	M	MP:0010506	prolonged RR interval	Ehhadh<tm1b(KOMP)Wtsi>/Ehhadh<tm1b(KOMP)Wtsi>	C57BL/6NTac-Ehhadh<tm1b(KOMP)Wtsi>/H	N	MGI:5576271
MGI:7471984	M	MP:0002059	abnormal seminal vesicle morphology	Emd<em1(IMPC)Kmpc>/Y	C57BL/6NTac-Emd<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471984	M	MP:0001566	increased circulating phosphate level	Emd<em1(IMPC)Kmpc>/Y	C57BL/6NTac-Emd<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471984	M	MP:0003960	increased lean body mass	Emd<em1(IMPC)Kmpc>/Y	C57BL/6NTac-Emd<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471985	F	MP:0001566	increased circulating phosphate level	Emd<em1(IMPC)Kmpc>/Emd<em1(IMPC)Kmpc>	C57BL/6NTac-Emd<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471985	F	MP:0009455	enhanced cued conditioning behavior	Emd<em1(IMPC)Kmpc>/Emd<em1(IMPC)Kmpc>	C57BL/6NTac-Emd<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7471986	M	MP:0008044	increased NK cell number	Emsy<em1(IMPC)Ccpcz>/Emsy<+>	C57BL/6NCrl-Emsy<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471986	M	MP:0002764	short tibia	Emsy<em1(IMPC)Ccpcz>/Emsy<+>	C57BL/6NCrl-Emsy<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471986	M	MP:0001146	abnormal testis morphology	Emsy<em1(IMPC)Ccpcz>/Emsy<+>	C57BL/6NCrl-Emsy<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471986	M	MP:0001157	small seminal vesicle	Emsy<em1(IMPC)Ccpcz>/Emsy<+>	C57BL/6NCrl-Emsy<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471986	F	MP:0005293	impaired glucose tolerance	Emsy<em1(IMPC)Ccpcz>/Emsy<+>	C57BL/6NCrl-Emsy<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471986	M	MP:0001148	enlarged testis	Emsy<em1(IMPC)Ccpcz>/Emsy<+>	C57BL/6NCrl-Emsy<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471986	M	MP:0002631	abnormal epididymis morphology	Emsy<em1(IMPC)Ccpcz>/Emsy<+>	C57BL/6NCrl-Emsy<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471986	M	MP:0000274	enlarged heart	Emsy<em1(IMPC)Ccpcz>/Emsy<+>	C57BL/6NCrl-Emsy<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471986	M	MP:0004931	enlarged epididymis	Emsy<em1(IMPC)Ccpcz>/Emsy<+>	C57BL/6NCrl-Emsy<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471986	M	MP:0002059	abnormal seminal vesicle morphology	Emsy<em1(IMPC)Ccpcz>/Emsy<+>	C57BL/6NCrl-Emsy<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471986	M	MP:0000266	abnormal heart morphology	Emsy<em1(IMPC)Ccpcz>/Emsy<+>	C57BL/6NCrl-Emsy<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471988	M	MP:0001417	decreased exploration in new environment	Eno2<em1(IMPC)H>/Eno2<em1(IMPC)H>	C57BL/6NTac-Eno2<em1(IMPC)H>/H	N	MGI:5576271
MGI:7471989	M	MP:0005293	impaired glucose tolerance	Eno3<em1(IMPC)Bay>/Eno3<+>	C57BL/6N-Eno3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471990	F	MP:0012122	abnormal iris transillumination	Esyt1<em1(IMPC)Hmgu>/Esyt1<em1(IMPC)Hmgu>	C57BL/6NCrl-Esyt1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471990	M	MP:0001406	abnormal gait	Esyt1<em1(IMPC)Hmgu>/Esyt1<em1(IMPC)Hmgu>	C57BL/6NCrl-Esyt1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471990	F	MP:0012121	sclerocornea	Esyt1<em1(IMPC)Hmgu>/Esyt1<em1(IMPC)Hmgu>	C57BL/6NCrl-Esyt1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471991	M	MP:0008259	abnormal optic disk morphology	Etfb<em1(IMPC)Hmgu>/Etfb<+>	C57BL/6NCrl-Etfb<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471991	M	MP:0002792	abnormal retina vasculature morphology	Etfb<em1(IMPC)Hmgu>/Etfb<+>	C57BL/6NCrl-Etfb<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471991	M	MP:0001289	persistence of hyaloid vascular system	Etfb<em1(IMPC)Hmgu>/Etfb<+>	C57BL/6NCrl-Etfb<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471991	M	MP:0002833	increased heart weight	Etfb<em1(IMPC)Hmgu>/Etfb<+>	C57BL/6NCrl-Etfb<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471991	M	MP:0004952	increased spleen weight	Etfb<em1(IMPC)Hmgu>/Etfb<+>	C57BL/6NCrl-Etfb<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471991	M	MP:0001325	abnormal retina morphology	Etfb<em1(IMPC)Hmgu>/Etfb<+>	C57BL/6NCrl-Etfb<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7471993	M	MP:0000274	enlarged heart	Fam120c<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Fam120c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471993	M	MP:0000438	abnormal cranium morphology	Fam120c<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Fam120c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471993	M	MP:0000266	abnormal heart morphology	Fam120c<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Fam120c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471993	M	MP:0003917	increased kidney weight	Fam120c<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Fam120c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471994	F	MP:0000703	abnormal thymus morphology	Fam120c<em1(IMPC)Ccpcz>/Fam120c<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam120c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471994	F	MP:0000691	enlarged spleen	Fam120c<em1(IMPC)Ccpcz>/Fam120c<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam120c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471994	F	MP:0000689	abnormal spleen morphology	Fam120c<em1(IMPC)Ccpcz>/Fam120c<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam120c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471994	F	MP:0000709	enlarged thymus	Fam120c<em1(IMPC)Ccpcz>/Fam120c<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam120c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471994	F	MP:0000627	abnormal mammary gland morphology	Fam120c<em1(IMPC)Ccpcz>/Fam120c<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam120c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471995	F	MP:0000598	abnormal liver morphology	Fam167a<em1(IMPC)Ccpcz>/Fam167a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam167a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471995	F	MP:0000367	abnormal coat/ hair morphology	Fam167a<em1(IMPC)Ccpcz>/Fam167a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam167a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471995	F	MP:0000709	enlarged thymus	Fam167a<em1(IMPC)Ccpcz>/Fam167a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam167a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471995	F	MP:0000691	enlarged spleen	Fam167a<em1(IMPC)Ccpcz>/Fam167a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam167a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471995	F	MP:0000689	abnormal spleen morphology	Fam167a<em1(IMPC)Ccpcz>/Fam167a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam167a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471995	F	MP:0001510	abnormal coat appearance	Fam167a<em1(IMPC)Ccpcz>/Fam167a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam167a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471995	M	MP:0001148	enlarged testis	Fam167a<em1(IMPC)Ccpcz>/Fam167a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam167a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471995	F	MP:0000703	abnormal thymus morphology	Fam167a<em1(IMPC)Ccpcz>/Fam167a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam167a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471995	F	MP:0010935	increased airway resistance	Fam167a<em1(IMPC)Ccpcz>/Fam167a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam167a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471995	F	MP:0011047	increased lung tissue damping	Fam167a<em1(IMPC)Ccpcz>/Fam167a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam167a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471995	M	MP:0001146	abnormal testis morphology	Fam167a<em1(IMPC)Ccpcz>/Fam167a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam167a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0002100	abnormal tooth morphology	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0000691	enlarged spleen	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0000759	abnormal skeletal muscle morphology	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0004002	abnormal jejunum morphology	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	M	MP:0000627	abnormal mammary gland morphology	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	M	MP:0002631	abnormal epididymis morphology	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0000709	enlarged thymus	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0000495	abnormal colon morphology	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0002060	abnormal skin morphology	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	M	MP:0001925	male infertility	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0001926	female infertility	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0003271	abnormal duodenum morphology	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	M	MP:0004931	enlarged epididymis	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	M	MP:0010052	increased grip strength	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0000702	enlarged lymph nodes	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0002339	abnormal lymph node morphology	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0000266	abnormal heart morphology	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0002581	abnormal ileum morphology	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0000703	abnormal thymus morphology	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0000689	abnormal spleen morphology	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471996	F	MP:0000274	enlarged heart	Fam227b<em1(IMPC)Ccpcz>/Fam227b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fam227b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471997	F	MP:0002574	increased vertical activity	Fam8a1<em1(IMPC)Bay>/Fam8a1<em1(IMPC)Bay>	C57BL/6N-Fam8a1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7471998	F	MP:0004906	enlarged uterus	Fat3<em1(IMPC)Ccpcz>/Fat3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fat3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471998	F	MP:0000709	enlarged thymus	Fat3<em1(IMPC)Ccpcz>/Fat3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fat3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471998	F	MP:0002060	abnormal skin morphology	Fat3<em1(IMPC)Ccpcz>/Fat3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fat3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471998	M	MP:0000274	enlarged heart	Fat3<em1(IMPC)Ccpcz>/Fat3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fat3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471998	F	MP:0000703	abnormal thymus morphology	Fat3<em1(IMPC)Ccpcz>/Fat3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fat3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471998	F	MP:0001120	abnormal uterus morphology	Fat3<em1(IMPC)Ccpcz>/Fat3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fat3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471998	M	MP:0010895	increased lung compliance	Fat3<em1(IMPC)Ccpcz>/Fat3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fat3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471998	F	MP:0004832	enlarged ovary	Fat3<em1(IMPC)Ccpcz>/Fat3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fat3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471998	M	MP:0011045	decreased lung elastance	Fat3<em1(IMPC)Ccpcz>/Fat3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fat3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471998	M	MP:0000266	abnormal heart morphology	Fat3<em1(IMPC)Ccpcz>/Fat3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fat3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471998	M	MP:0002953	thick ventricular wall	Fat3<em1(IMPC)Ccpcz>/Fat3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fat3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471998	M	MP:0000759	abnormal skeletal muscle morphology	Fat3<em1(IMPC)Ccpcz>/Fat3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fat3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7471998	F	MP:0001126	abnormal ovary morphology	Fat3<em1(IMPC)Ccpcz>/Fat3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fat3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472000	M	MP:0005293	impaired glucose tolerance	Fbxl9<em1(IMPC)Bay>/Fbxl9<em1(IMPC)Bay>	C57BL/6N-Fbxl9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472001	F	MP:0020870	decreased thigmotaxis	Fbxo28<em1(IMPC)Mhzh>/Fbxo28<+>	C57BL/6N-Fbxo28<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472001	F	MP:0010052	increased grip strength	Fbxo28<em1(IMPC)Mhzh>/Fbxo28<+>	C57BL/6N-Fbxo28<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472001	F	MP:0004924	abnormal behavior	Fbxo28<em1(IMPC)Mhzh>/Fbxo28<+>	C57BL/6N-Fbxo28<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472001	M	MP:0002606	increased basophil cell number	Fbxo28<em1(IMPC)Mhzh>/Fbxo28<+>	C57BL/6N-Fbxo28<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472001	M	MP:0005011	increased eosinophil cell number	Fbxo28<em1(IMPC)Mhzh>/Fbxo28<+>	C57BL/6N-Fbxo28<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472002	F	MP:0010392	prolonged QRS complex duration	Fbxo42<em1(IMPC)J>/Fbxo42<+>	C57BL/6NJ-Fbxo42<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472002	F	MP:0002942	decreased circulating alanine transaminase level	Fbxo42<em1(IMPC)J>/Fbxo42<+>	C57BL/6NJ-Fbxo42<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472002	F	MP:0005635	decreased circulating bilirubin level	Fbxo42<em1(IMPC)J>/Fbxo42<+>	C57BL/6NJ-Fbxo42<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472002	F	MP:0005505	thrombocytosis	Fbxo42<em1(IMPC)J>/Fbxo42<+>	C57BL/6NJ-Fbxo42<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472002	M	MP:0010123	increased bone mineral content	Fbxo42<em1(IMPC)J>/Fbxo42<+>	C57BL/6NJ-Fbxo42<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472003	F	MP:0001304	cataract	Fbxo5<em1(IMPC)Mbp>/Fbxo5<+>	C57BL/6NCrl-Fbxo5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472003	M	MP:0002135	abnormal kidney morphology	Fbxo5<em1(IMPC)Mbp>/Fbxo5<+>	C57BL/6NCrl-Fbxo5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472003	F	MP:0002060	abnormal skin morphology	Fbxo5<em1(IMPC)Mbp>/Fbxo5<+>	C57BL/6NCrl-Fbxo5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472003	M	MP:0003068	enlarged kidney	Fbxo5<em1(IMPC)Mbp>/Fbxo5<+>	C57BL/6NCrl-Fbxo5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472005	M	MP:0000266	abnormal heart morphology	Fbxw25<em1(IMPC)Ccpcz>/Fbxw25<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxw25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472005	M	MP:0000274	enlarged heart	Fbxw25<em1(IMPC)Ccpcz>/Fbxw25<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxw25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472005	F	MP:0000703	abnormal thymus morphology	Fbxw25<em1(IMPC)Ccpcz>/Fbxw25<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxw25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472005	F	MP:0000709	enlarged thymus	Fbxw25<em1(IMPC)Ccpcz>/Fbxw25<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fbxw25<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472006	F	MP:0005343	increased circulating aspartate transaminase level	Fcrl2<em1(IMPC)H>/Fcrl2<em1(IMPC)H>	C57BL/6NTac-Fcrl2<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472006	F	MP:0010090	increased circulating creatine kinase level	Fcrl2<em1(IMPC)H>/Fcrl2<em1(IMPC)H>	C57BL/6NTac-Fcrl2<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472006	F	MP:0001566	increased circulating phosphate level	Fcrl2<em1(IMPC)H>/Fcrl2<em1(IMPC)H>	C57BL/6NTac-Fcrl2<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472008	F	MP:0010052	increased grip strength	Fgf17<em1(IMPC)H>/Fgf17<em1(IMPC)H>	C57BL/6NTac-Fgf17<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472009	M	MP:0010052	increased grip strength	Foxb2<em1(IMPC)J>/Foxb2<+>	C57BL/6NJ-Foxb2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472010	F	MP:0003733	abnormal retina inner nuclear layer morphology	Fscb<em1(IMPC)Bay>/Fscb<em1(IMPC)Bay>	C57BL/6N-Fscb<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472010	F	MP:0001399	hyperactivity	Fscb<em1(IMPC)Bay>/Fscb<em1(IMPC)Bay>	C57BL/6N-Fscb<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472010	F	MP:0003731	abnormal retina outer nuclear layer morphology	Fscb<em1(IMPC)Bay>/Fscb<em1(IMPC)Bay>	C57BL/6N-Fscb<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472010	F	MP:0002574	increased vertical activity	Fscb<em1(IMPC)Bay>/Fscb<em1(IMPC)Bay>	C57BL/6N-Fscb<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472011	F	MP:0002797	increased thigmotaxis	Gal3st1<em1(IMPC)Rbrc>/Gal3st1<em1(IMPC)Rbrc>	C57BL/6NJcl-Gal3st1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7472011	M	MP:0005292	improved glucose tolerance	Gal3st1<em1(IMPC)Rbrc>/Gal3st1<em1(IMPC)Rbrc>	C57BL/6NJcl-Gal3st1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7472011	F	MP:0001399	hyperactivity	Gal3st1<em1(IMPC)Rbrc>/Gal3st1<em1(IMPC)Rbrc>	C57BL/6NJcl-Gal3st1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7472011	F	MP:0004924	abnormal behavior	Gal3st1<em1(IMPC)Rbrc>/Gal3st1<em1(IMPC)Rbrc>	C57BL/6NJcl-Gal3st1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7472011	M	MP:0004930	small epididymis	Gal3st1<em1(IMPC)Rbrc>/Gal3st1<em1(IMPC)Rbrc>	C57BL/6NJcl-Gal3st1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7472011	F	MP:0002764	short tibia	Gal3st1<em1(IMPC)Rbrc>/Gal3st1<em1(IMPC)Rbrc>	C57BL/6NJcl-Gal3st1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7472011	M	MP:0001146	abnormal testis morphology	Gal3st1<em1(IMPC)Rbrc>/Gal3st1<em1(IMPC)Rbrc>	C57BL/6NJcl-Gal3st1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7472011	M	MP:0001147	small testis	Gal3st1<em1(IMPC)Rbrc>/Gal3st1<em1(IMPC)Rbrc>	C57BL/6NJcl-Gal3st1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7472011	M	MP:0001363	increased anxiety-related response	Gal3st1<em1(IMPC)Rbrc>/Gal3st1<em1(IMPC)Rbrc>	C57BL/6NJcl-Gal3st1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7472011	M	MP:0002631	abnormal epididymis morphology	Gal3st1<em1(IMPC)Rbrc>/Gal3st1<em1(IMPC)Rbrc>	C57BL/6NJcl-Gal3st1<em1(IMPC)Rbrc>/Rbrc	N	MGI:5576271
MGI:7472012	F	MP:0001293	anophthalmia	Garnl3<em1(IMPC)Bay>/Garnl3<+>	C57BL/6N-Garnl3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472013	M	MP:0001402	decreased locomotor activity	Gcg<em1(IMPC)H>/Gcg<em1(IMPC)H>	C57BL/6NTac-Gcg<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472016	F	MP:0003795	abnormal bone structure	Gdf5<em1(IMPC)Bay>/Gdf5<em1(IMPC)Bay>	C57BL/6N-Gdf5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472017	M	MP:0011047	increased lung tissue damping	Gdf6<em1(IMPC)Ccpcz>/Gdf6<+>	C57BL/6NCrl-Gdf6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472017	F	MP:0000709	enlarged thymus	Gdf6<em1(IMPC)Ccpcz>/Gdf6<+>	C57BL/6NCrl-Gdf6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472017	F	MP:0000703	abnormal thymus morphology	Gdf6<em1(IMPC)Ccpcz>/Gdf6<+>	C57BL/6NCrl-Gdf6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472017	F	MP:0002152	abnormal brain morphology	Gdf6<em1(IMPC)Ccpcz>/Gdf6<+>	C57BL/6NCrl-Gdf6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472017	F	MP:0001891	hydrocephaly	Gdf6<em1(IMPC)Ccpcz>/Gdf6<+>	C57BL/6NCrl-Gdf6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472020	F	MP:0011100	preweaning lethality, complete penetrance	Gigyf1<em1(IMPC)Bay>/Gigyf1<em1(IMPC)Bay>	C57BL/6N-Gigyf1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472021	F	MP:0002699	abnormal vitreous body morphology	Glipr1<em1(IMPC)Hmgu>/Glipr1<em1(IMPC)Hmgu>	C57BL/6NCrl-Glipr1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472023	F	MP:0005553	increased circulating creatinine level	Gm5127<em1(IMPC)J>/Gm5127<em1(IMPC)J>	C57BL/6NJ-Gm5127<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472023	F	MP:0005343	increased circulating aspartate transaminase level	Gm5127<em1(IMPC)J>/Gm5127<em1(IMPC)J>	C57BL/6NJ-Gm5127<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472024	M	MP:0001488	increased startle reflex	Gmeb2<em1(IMPC)J>/Gmeb2<+>	C57BL/6NJ-Gmeb2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472024	M	MP:0003960	increased lean body mass	Gmeb2<em1(IMPC)J>/Gmeb2<+>	C57BL/6NJ-Gmeb2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472025	M	MP:0002608	increased hematocrit	Gpalpp1<em1(IMPC)Hmgu>/Gpalpp1<em1(IMPC)Hmgu>	C57BL/6NCrl-Gpalpp1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472025	M	MP:0003131	increased erythrocyte cell number	Gpalpp1<em1(IMPC)Hmgu>/Gpalpp1<em1(IMPC)Hmgu>	C57BL/6NCrl-Gpalpp1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472025	M	MP:0005564	increased hemoglobin content	Gpalpp1<em1(IMPC)Hmgu>/Gpalpp1<em1(IMPC)Hmgu>	C57BL/6NCrl-Gpalpp1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472026	F	MP:0000195	decreased circulating calcium level	Gpr63<tm1.1(KOMP)Vlcg>/Gpr63<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpr63<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7472026	F	MP:0002941	increased circulating alanine transaminase level	Gpr63<tm1.1(KOMP)Vlcg>/Gpr63<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpr63<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7472027	M	MP:0002152	abnormal brain morphology	Gpr83<em1(IMPC)Ccpcz>/Gpr83<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpr83<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472027	F	MP:0008040	decreased NK T cell number	Gpr83<em1(IMPC)Ccpcz>/Gpr83<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpr83<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472027	F	MP:0013519	decreased CD4-positive NK T cell number	Gpr83<em1(IMPC)Ccpcz>/Gpr83<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpr83<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472027	F	MP:0000691	enlarged spleen	Gpr83<em1(IMPC)Ccpcz>/Gpr83<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpr83<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472027	M	MP:0001262	decreased body weight	Gpr83<em1(IMPC)Ccpcz>/Gpr83<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpr83<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472027	F	MP:0013522	decreased memory-marker CD4-positive NK T cell number	Gpr83<em1(IMPC)Ccpcz>/Gpr83<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpr83<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472027	M	MP:0000598	abnormal liver morphology	Gpr83<em1(IMPC)Ccpcz>/Gpr83<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpr83<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472028	F	MP:0020421	increased freezing behavior	Grk3<em1(IMPC)Mbp>/Grk3<em1(IMPC)Mbp>	C57BL/6NCrl-Grk3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472029	M	MP:0000157	abnormal sternum morphology	Gsdmc<em1(IMPC)Tcp>/Gsdmc<em1(IMPC)Tcp>	C57BL/6NCrl-Gsdmc<em1(IMPC)Tcp>/TcpMmucd	N	MGI:5576271
MGI:7472029	F	MP:0000702	enlarged lymph nodes	Gsdmc<em1(IMPC)Tcp>/Gsdmc<em1(IMPC)Tcp>	C57BL/6NCrl-Gsdmc<em1(IMPC)Tcp>/TcpMmucd	N	MGI:5576271
MGI:7472034	M	MP:0005559	increased circulating glucose level	Haao<tm2b(KOMP)Mbp>/Haao<tm2b(KOMP)Mbp>	C57BL/6N-Haao<tm2b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7472034	F	MP:0010123	increased bone mineral content	Haao<tm2b(KOMP)Mbp>/Haao<tm2b(KOMP)Mbp>	C57BL/6N-Haao<tm2b(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7472035	F	MP:0002060	abnormal skin morphology	Hacd1<em1(IMPC)Mbp>/Hacd1<+>	C57BL/6NCrl-Hacd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472035	F	MP:0001325	abnormal retina morphology	Hacd1<em1(IMPC)Mbp>/Hacd1<+>	C57BL/6NCrl-Hacd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472036	F	MP:0003984	embryonic growth retardation	Hacd1<em1(IMPC)Mbp>/Hacd1<em1(IMPC)Mbp>	C57BL/6NCrl-Hacd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472036	F	MP:0001614	abnormal blood vessel morphology	Hacd1<em1(IMPC)Mbp>/Hacd1<em1(IMPC)Mbp>	C57BL/6NCrl-Hacd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472036	F	MP:0001297	microphthalmia	Hacd1<em1(IMPC)Mbp>/Hacd1<em1(IMPC)Mbp>	C57BL/6NCrl-Hacd1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472037	M	MP:0002941	increased circulating alanine transaminase level	Hdac11<em1(IMPC)Kmpc>/Hdac11<em1(IMPC)Kmpc>	C57BL/6NTac-Hdac11<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472037	F	MP:0001257	increased body length	Hdac11<em1(IMPC)Kmpc>/Hdac11<em1(IMPC)Kmpc>	C57BL/6NTac-Hdac11<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472039	M	MP:0002339	abnormal lymph node morphology	Heph<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Heph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472039	M	MP:0000274	enlarged heart	Heph<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Heph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472039	M	MP:0000266	abnormal heart morphology	Heph<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Heph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472039	M	MP:0008810	increased circulating iron level	Heph<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Heph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472039	M	MP:0000702	enlarged lymph nodes	Heph<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Heph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472040	F	MP:0008810	increased circulating iron level	Heph<em1(IMPC)Ccpcz>/Heph<em1(IMPC)Ccpcz>	C57BL/6NCrl-Heph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472040	F	MP:0002339	abnormal lymph node morphology	Heph<em1(IMPC)Ccpcz>/Heph<em1(IMPC)Ccpcz>	C57BL/6NCrl-Heph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472040	F	MP:0000702	enlarged lymph nodes	Heph<em1(IMPC)Ccpcz>/Heph<em1(IMPC)Ccpcz>	C57BL/6NCrl-Heph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472040	F	MP:0001566	increased circulating phosphate level	Heph<em1(IMPC)Ccpcz>/Heph<em1(IMPC)Ccpcz>	C57BL/6NCrl-Heph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472040	F	MP:0005343	increased circulating aspartate transaminase level	Heph<em1(IMPC)Ccpcz>/Heph<em1(IMPC)Ccpcz>	C57BL/6NCrl-Heph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472041	F	MP:0005140	decreased cardiac muscle contractility	Hilpda<em1(IMPC)Mhzh>/Hilpda<em1(IMPC)Mhzh>	C57BL/6N-Hilpda<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472041	M	MP:0000280	thin ventricular wall	Hilpda<em1(IMPC)Mhzh>/Hilpda<em1(IMPC)Mhzh>	C57BL/6N-Hilpda<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472042	M	MP:0011110	preweaning lethality, incomplete penetrance	Hivep1<tm1(KOMP)Mbp>/Hivep1<tm1(KOMP)Mbp>	C57BL/6N-Hivep1<tm1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472043	F	MP:0020870	decreased thigmotaxis	Hoga1<em1(IMPC)Bay>/Hoga1<em1(IMPC)Bay>	C57BL/6N-Hoga1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472043	F	MP:0001399	hyperactivity	Hoga1<em1(IMPC)Bay>/Hoga1<em1(IMPC)Bay>	C57BL/6N-Hoga1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472043	F	MP:0001364	decreased anxiety-related response	Hoga1<em1(IMPC)Bay>/Hoga1<em1(IMPC)Bay>	C57BL/6N-Hoga1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472046	M	MP:0011110	preweaning lethality, incomplete penetrance	Htra2<tm1.1(KOMP)Vlcg>/Htra2<tm1.1(KOMP)Vlcg>	C57BL/6N-Htra2<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7472048	M	MP:0002059	abnormal seminal vesicle morphology	Ik<em2(IMPC)Kmpc>/Ik<+>	C57BL/6NTac-Ik<em2(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472048	M	MP:0010024	increased total body fat amount	Ik<em2(IMPC)Kmpc>/Ik<+>	C57BL/6NTac-Ik<em2(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472048	M	MP:0010052	increased grip strength	Ik<em2(IMPC)Kmpc>/Ik<+>	C57BL/6NTac-Ik<em2(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472048	M	MP:0003960	increased lean body mass	Ik<em2(IMPC)Kmpc>/Ik<+>	C57BL/6NTac-Ik<em2(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472050	M	MP:0000689	abnormal spleen morphology	Il17rc<em1(IMPC)Mbp>/Il17rc<em1(IMPC)Mbp>	C57BL/6NCrl-Il17rc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472050	F	MP:0002135	abnormal kidney morphology	Il17rc<em1(IMPC)Mbp>/Il17rc<em1(IMPC)Mbp>	C57BL/6NCrl-Il17rc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472050	F	MP:0001126	abnormal ovary morphology	Il17rc<em1(IMPC)Mbp>/Il17rc<em1(IMPC)Mbp>	C57BL/6NCrl-Il17rc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472050	M	MP:0000691	enlarged spleen	Il17rc<em1(IMPC)Mbp>/Il17rc<em1(IMPC)Mbp>	C57BL/6NCrl-Il17rc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472050	M	MP:0002644	decreased circulating triglyceride level	Il17rc<em1(IMPC)Mbp>/Il17rc<em1(IMPC)Mbp>	C57BL/6NCrl-Il17rc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472050	F	MP:0001258	decreased body length	Il17rc<em1(IMPC)Mbp>/Il17rc<em1(IMPC)Mbp>	C57BL/6NCrl-Il17rc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472050	F	MP:0002092	abnormal eye morphology	Il17rc<em1(IMPC)Mbp>/Il17rc<em1(IMPC)Mbp>	C57BL/6NCrl-Il17rc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472050	F	MP:0002989	small kidney	Il17rc<em1(IMPC)Mbp>/Il17rc<em1(IMPC)Mbp>	C57BL/6NCrl-Il17rc<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472051	M	MP:0001489	decreased startle reflex	Il20<em1(IMPC)Mbp>/Il20<em1(IMPC)Mbp>	C57BL/6NCrl-Il20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472051	M	MP:0002941	increased circulating alanine transaminase level	Il20<em1(IMPC)Mbp>/Il20<em1(IMPC)Mbp>	C57BL/6NCrl-Il20<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472052	M	MP:0000691	enlarged spleen	Inpp5j<em1(IMPC)Mbp>/Inpp5j<em1(IMPC)Mbp>	C57BL/6NCrl-Inpp5j<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472052	F	MP:0001293	anophthalmia	Inpp5j<em1(IMPC)Mbp>/Inpp5j<em1(IMPC)Mbp>	C57BL/6NCrl-Inpp5j<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472052	M	MP:0000689	abnormal spleen morphology	Inpp5j<em1(IMPC)Mbp>/Inpp5j<em1(IMPC)Mbp>	C57BL/6NCrl-Inpp5j<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472052	M	MP:0001200	thick skin	Inpp5j<em1(IMPC)Mbp>/Inpp5j<em1(IMPC)Mbp>	C57BL/6NCrl-Inpp5j<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472053	F	MP:0009709	hydrometra	Islr<em1(IMPC)Hmgu>/Islr<em1(IMPC)Hmgu>	C57BL/6NCrl-Islr<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472055	M	MP:0001399	hyperactivity	Itgb1<em1(IMPC)Bay>/Itgb1<+>	C57BL/6N-Itgb1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472058	F	MP:0011110	preweaning lethality, incomplete penetrance	Jazf1<tm1b(EUCOMM)Wtsi>/Jazf1<tm1b(EUCOMM)Wtsi>	C57BL/6N-Jazf1<tm1b(EUCOMM)Wtsi>/Ucd	N	MGI:5576271
MGI:7472059	F	MP:0009476	enlarged cecum	Kbtbd12<em1(IMPC)Mbp>/Kbtbd12<em1(IMPC)Mbp>	C57BL/6NCrl-Kbtbd12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472059	F	MP:0000494	abnormal cecum morphology	Kbtbd12<em1(IMPC)Mbp>/Kbtbd12<em1(IMPC)Mbp>	C57BL/6NCrl-Kbtbd12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472060	M	MP:0000219	increased neutrophil cell number	Kbtbd3<em1(IMPC)Ccpcz>/Kbtbd3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kbtbd3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472060	F	MP:0000709	enlarged thymus	Kbtbd3<em1(IMPC)Ccpcz>/Kbtbd3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kbtbd3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472060	F	MP:0000703	abnormal thymus morphology	Kbtbd3<em1(IMPC)Ccpcz>/Kbtbd3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kbtbd3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	F	MP:0009709	hydrometra	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0002059	abnormal seminal vesicle morphology	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0001148	enlarged testis	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0000706	small thymus	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0002932	abnormal joint morphology	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0002875	decreased erythrocyte cell number	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	F	MP:0000709	enlarged thymus	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	F	MP:0002060	abnormal skin morphology	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0001146	abnormal testis morphology	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0002874	decreased hemoglobin content	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0001157	small seminal vesicle	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0000601	small liver	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0000266	abnormal heart morphology	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0013279	increased fasting circulating glucose level	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0002188	small heart	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0000495	abnormal colon morphology	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0000492	abnormal rectum morphology	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0009476	enlarged cecum	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472062	M	MP:0000598	abnormal liver morphology	Kcnn4<em1(IMPC)Ccpcz>/Kcnn4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kcnn4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472063	M	MP:0002135	abnormal kidney morphology	Khsrp<em1(IMPC)Mbp>/Khsrp<em1(IMPC)Mbp>	C57BL/6NCrl-Khsrp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472063	M	MP:0010067	increased red blood cell distribution width	Khsrp<em1(IMPC)Mbp>/Khsrp<em1(IMPC)Mbp>	C57BL/6NCrl-Khsrp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472063	M	MP:0009552	urinary bladder obstruction	Khsrp<em1(IMPC)Mbp>/Khsrp<em1(IMPC)Mbp>	C57BL/6NCrl-Khsrp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472063	M	MP:0003068	enlarged kidney	Khsrp<em1(IMPC)Mbp>/Khsrp<em1(IMPC)Mbp>	C57BL/6NCrl-Khsrp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472065	F	MP:0001399	hyperactivity	Kif2a<em1(IMPC)Mbp>/Kif2a<+>	C57BL/6NCrl-Kif2a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472067	M	MP:0005568	increased circulating total protein level	Kif5c<tm1dIcs>/Kif5c<+>	C57BL/6N-Kif5c<tm1dIcs>/Ics	N	MGI:5576271
MGI:7472067	F	MP:0005016	decreased lymphocyte cell number	Kif5c<tm1dIcs>/Kif5c<+>	C57BL/6N-Kif5c<tm1dIcs>/Ics	N	MGI:5576271
MGI:7472067	F	MP:0005011	increased eosinophil cell number	Kif5c<tm1dIcs>/Kif5c<+>	C57BL/6N-Kif5c<tm1dIcs>/Ics	N	MGI:5576271
MGI:7472068	F	MP:0001926	female infertility	Kif6<em1(IMPC)Ccpcz>/Kif6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472068	M	MP:0001147	small testis	Kif6<em1(IMPC)Ccpcz>/Kif6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472068	M	MP:0001146	abnormal testis morphology	Kif6<em1(IMPC)Ccpcz>/Kif6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472068	F	MP:0002188	small heart	Kif6<em1(IMPC)Ccpcz>/Kif6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472068	F	MP:0009709	hydrometra	Kif6<em1(IMPC)Ccpcz>/Kif6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472068	F	MP:0000774	decreased brain size	Kif6<em1(IMPC)Ccpcz>/Kif6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472068	M	MP:0001925	male infertility	Kif6<em1(IMPC)Ccpcz>/Kif6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472068	F	MP:0000266	abnormal heart morphology	Kif6<em1(IMPC)Ccpcz>/Kif6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472068	F	MP:0001120	abnormal uterus morphology	Kif6<em1(IMPC)Ccpcz>/Kif6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Kif6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472069	M	MP:0010053	decreased grip strength	Klf4<em1(IMPC)Kmpc>/Klf4<em1(IMPC)Kmpc>	C57BL/6NTac-Klf4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472072	M	MP:0002059	abnormal seminal vesicle morphology	Krt26<em1(IMPC)Kmpc>/Krt26<em1(IMPC)Kmpc>	C57BL/6NTac-Krt26<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472072	M	MP:0002834	decreased heart weight	Krt26<em1(IMPC)Kmpc>/Krt26<em1(IMPC)Kmpc>	C57BL/6NTac-Krt26<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472072	F	MP:0002110	abnormal digit morphology	Krt26<em1(IMPC)Kmpc>/Krt26<em1(IMPC)Kmpc>	C57BL/6NTac-Krt26<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472072	M	MP:0011239	abnormal skin coloration	Krt26<em1(IMPC)Kmpc>/Krt26<em1(IMPC)Kmpc>	C57BL/6NTac-Krt26<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472073	F	MP:0005565	increased blood urea nitrogen level	Krt32<em1(IMPC)Kmpc>/Krt32<em1(IMPC)Kmpc>	C57BL/6NTac-Krt32<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472073	F	MP:0005178	increased circulating cholesterol level	Krt32<em1(IMPC)Kmpc>/Krt32<em1(IMPC)Kmpc>	C57BL/6NTac-Krt32<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472073	F	MP:0001415	increased exploration in new environment	Krt32<em1(IMPC)Kmpc>/Krt32<em1(IMPC)Kmpc>	C57BL/6NTac-Krt32<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472073	F	MP:0005564	increased hemoglobin content	Krt32<em1(IMPC)Kmpc>/Krt32<em1(IMPC)Kmpc>	C57BL/6NTac-Krt32<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472073	M	MP:0002059	abnormal seminal vesicle morphology	Krt32<em1(IMPC)Kmpc>/Krt32<em1(IMPC)Kmpc>	C57BL/6NTac-Krt32<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472074	F	MP:0000709	enlarged thymus	Krt34<em1(IMPC)Ccpcz>/Krt34<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt34<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472074	M	MP:0000691	enlarged spleen	Krt34<em1(IMPC)Ccpcz>/Krt34<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt34<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472074	M	MP:0000266	abnormal heart morphology	Krt34<em1(IMPC)Ccpcz>/Krt34<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt34<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472074	M	MP:0000702	enlarged lymph nodes	Krt34<em1(IMPC)Ccpcz>/Krt34<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt34<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472074	F	MP:0000703	abnormal thymus morphology	Krt34<em1(IMPC)Ccpcz>/Krt34<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt34<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472074	M	MP:0002339	abnormal lymph node morphology	Krt34<em1(IMPC)Ccpcz>/Krt34<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt34<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472074	M	MP:0001402	decreased locomotor activity	Krt34<em1(IMPC)Ccpcz>/Krt34<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt34<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472074	M	MP:0003917	increased kidney weight	Krt34<em1(IMPC)Ccpcz>/Krt34<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt34<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472074	F	MP:0003020	decreased circulating chloride level	Krt34<em1(IMPC)Ccpcz>/Krt34<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt34<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472074	M	MP:0000689	abnormal spleen morphology	Krt34<em1(IMPC)Ccpcz>/Krt34<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt34<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472074	M	MP:0000274	enlarged heart	Krt34<em1(IMPC)Ccpcz>/Krt34<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt34<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472075	M	MP:0002059	abnormal seminal vesicle morphology	Krt35<em1(IMPC)Kmpc>/Krt35<em1(IMPC)Kmpc>	C57BL/6NTac-Krt35<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472075	M	MP:0002075	abnormal coat/hair pigmentation	Krt35<em1(IMPC)Kmpc>/Krt35<em1(IMPC)Kmpc>	C57BL/6NTac-Krt35<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472077	M	MP:0000218	increased leukocyte cell number	Ky<em1(IMPC)J>/Ky<+>	C57BL/6NJ-Ky<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472080	M	MP:0002075	abnormal coat/hair pigmentation	Ldaf1<em1(IMPC)Kmpc>/Ldaf1<em1(IMPC)Kmpc>	C57BL/6NTac-Ldaf1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472080	F	MP:0001297	microphthalmia	Ldaf1<em1(IMPC)Kmpc>/Ldaf1<em1(IMPC)Kmpc>	C57BL/6NTac-Ldaf1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472080	F	MP:0002092	abnormal eye morphology	Ldaf1<em1(IMPC)Kmpc>/Ldaf1<em1(IMPC)Kmpc>	C57BL/6NTac-Ldaf1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472080	F	MP:0003271	abnormal duodenum morphology	Ldaf1<em1(IMPC)Kmpc>/Ldaf1<em1(IMPC)Kmpc>	C57BL/6NTac-Ldaf1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472080	M	MP:0003960	increased lean body mass	Ldaf1<em1(IMPC)Kmpc>/Ldaf1<em1(IMPC)Kmpc>	C57BL/6NTac-Ldaf1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472081	F	MP:0004924	abnormal behavior	Lemd3<em1(IMPC)Bay>/Lemd3<+>	C57BL/6N-Lemd3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472081	F	MP:0001402	decreased locomotor activity	Lemd3<em1(IMPC)Bay>/Lemd3<+>	C57BL/6N-Lemd3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472081	F	MP:0020870	decreased thigmotaxis	Lemd3<em1(IMPC)Bay>/Lemd3<+>	C57BL/6N-Lemd3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472083	F	MP:0000063	decreased bone mineral density	Letmd1<em1(IMPC)Kmpc>/Letmd1<em1(IMPC)Kmpc>	C57BL/6NTac-Letmd1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472083	F	MP:0010024	increased total body fat amount	Letmd1<em1(IMPC)Kmpc>/Letmd1<em1(IMPC)Kmpc>	C57BL/6NTac-Letmd1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472083	M	MP:0009142	decreased prepulse inhibition	Letmd1<em1(IMPC)Kmpc>/Letmd1<em1(IMPC)Kmpc>	C57BL/6NTac-Letmd1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472083	F	MP:0002833	increased heart weight	Letmd1<em1(IMPC)Kmpc>/Letmd1<em1(IMPC)Kmpc>	C57BL/6NTac-Letmd1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472083	F	MP:0013279	increased fasting circulating glucose level	Letmd1<em1(IMPC)Kmpc>/Letmd1<em1(IMPC)Kmpc>	C57BL/6NTac-Letmd1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472084	M	MP:0013648	increased CD11b-high dendritic cell number	Lgr5<em1(IMPC)Kmpc>/Lgr5<+>	C57BL/6NTac-Lgr5<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472084	F	MP:0005344	increased circulating bilirubin level	Lgr5<em1(IMPC)Kmpc>/Lgr5<+>	C57BL/6NTac-Lgr5<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472086	F	MP:0000703	abnormal thymus morphology	Lgr6<em1(IMPC)Ccpcz>/Lgr6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lgr6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472086	F	MP:0002092	abnormal eye morphology	Lgr6<em1(IMPC)Ccpcz>/Lgr6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lgr6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472086	M	MP:0000266	abnormal heart morphology	Lgr6<em1(IMPC)Ccpcz>/Lgr6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lgr6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472086	M	MP:0000274	enlarged heart	Lgr6<em1(IMPC)Ccpcz>/Lgr6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lgr6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472086	M	MP:0002100	abnormal tooth morphology	Lgr6<em1(IMPC)Ccpcz>/Lgr6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lgr6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472086	F	MP:0000709	enlarged thymus	Lgr6<em1(IMPC)Ccpcz>/Lgr6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lgr6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472087	M	MP:0002942	decreased circulating alanine transaminase level	Lhfpl4<em1(IMPC)H>/Lhfpl4<+>	C57BL/6NTac-Lhfpl4<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472088	F	MP:0002092	abnormal eye morphology	Lhfpl6<em1(IMPC)Mbp>/Lhfpl6<em1(IMPC)Mbp>	C57BL/6NCrl-Lhfpl6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472088	M	MP:0001402	decreased locomotor activity	Lhfpl6<em1(IMPC)Mbp>/Lhfpl6<em1(IMPC)Mbp>	C57BL/6NCrl-Lhfpl6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472088	M	MP:0000266	abnormal heart morphology	Lhfpl6<em1(IMPC)Mbp>/Lhfpl6<em1(IMPC)Mbp>	C57BL/6NCrl-Lhfpl6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472088	F	MP:0002060	abnormal skin morphology	Lhfpl6<em1(IMPC)Mbp>/Lhfpl6<em1(IMPC)Mbp>	C57BL/6NCrl-Lhfpl6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472088	F	MP:0001293	anophthalmia	Lhfpl6<em1(IMPC)Mbp>/Lhfpl6<em1(IMPC)Mbp>	C57BL/6NCrl-Lhfpl6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472088	F	MP:0001297	microphthalmia	Lhfpl6<em1(IMPC)Mbp>/Lhfpl6<em1(IMPC)Mbp>	C57BL/6NCrl-Lhfpl6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472088	M	MP:0000274	enlarged heart	Lhfpl6<em1(IMPC)Mbp>/Lhfpl6<em1(IMPC)Mbp>	C57BL/6NCrl-Lhfpl6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472089	M	MP:0002833	increased heart weight	Lilrb4b<em1(IMPC)J>/Lilrb4b<em1(IMPC)J>	C57BL/6NJ-Lilrb4b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472091	F	MP:0004357	long tibia	Lingo2<em1(IMPC)Kmpc>/Lingo2<em1(IMPC)Kmpc>	C57BL/6NTac-Lingo2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472091	F	MP:0000598	abnormal liver morphology	Lingo2<em1(IMPC)Kmpc>/Lingo2<em1(IMPC)Kmpc>	C57BL/6NTac-Lingo2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472091	F	MP:0010025	decreased total body fat amount	Lingo2<em1(IMPC)Kmpc>/Lingo2<em1(IMPC)Kmpc>	C57BL/6NTac-Lingo2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472091	F	MP:0001120	abnormal uterus morphology	Lingo2<em1(IMPC)Kmpc>/Lingo2<em1(IMPC)Kmpc>	C57BL/6NTac-Lingo2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472091	F	MP:0001257	increased body length	Lingo2<em1(IMPC)Kmpc>/Lingo2<em1(IMPC)Kmpc>	C57BL/6NTac-Lingo2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472091	F	MP:0009709	hydrometra	Lingo2<em1(IMPC)Kmpc>/Lingo2<em1(IMPC)Kmpc>	C57BL/6NTac-Lingo2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472092	F	MP:0001406	abnormal gait	Lingo3<em1(IMPC)Wtsi>/Lingo3<em1(IMPC)Wtsi>	C57BL/6NCrl-Lingo3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:7472095	M	MP:0000266	abnormal heart morphology	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472095	M	MP:0001925	male infertility	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472095	F	MP:0001926	female infertility	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472095	M	MP:0003917	increased kidney weight	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472095	F	MP:0002966	decreased circulating alkaline phosphatase level	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472095	M	MP:0000274	enlarged heart	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472095	F	MP:0011971	increased circulating lactate dehydrogenase level	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472095	F	MP:0010090	increased circulating creatine kinase level	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472095	F	MP:0004599	abnormal vertebral arch morphology	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472095	F	MP:0000689	abnormal spleen morphology	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472095	F	MP:0002941	increased circulating alanine transaminase level	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472095	F	MP:0000703	abnormal thymus morphology	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472095	M	MP:0001406	abnormal gait	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472095	F	MP:0000709	enlarged thymus	Lrig3<em1(IMPC)Ccpcz>/Lrig3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Lrig3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472097	M	MP:0002965	increased circulating serum albumin level	Ltk<em1(IMPC)H>/Ltk<em1(IMPC)H>	C57BL/6NTac-Ltk<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472097	M	MP:0005568	increased circulating total protein level	Ltk<em1(IMPC)H>/Ltk<em1(IMPC)H>	C57BL/6NTac-Ltk<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472098	M	MP:0005333	decreased heart rate	Ly6g6f<em1(IMPC)Hmgu>/Ly6g6f<em1(IMPC)Hmgu>	C57BL/6NCrl-Ly6g6f<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472100	M	MP:0004599	abnormal vertebral arch morphology	Marveld3<em1(IMPC)Ccpcz>/Marveld3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Marveld3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472100	F	MP:0000266	abnormal heart morphology	Marveld3<em1(IMPC)Ccpcz>/Marveld3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Marveld3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472100	M	MP:0000150	abnormal rib morphology	Marveld3<em1(IMPC)Ccpcz>/Marveld3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Marveld3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472100	M	MP:0003036	vertebral transformation	Marveld3<em1(IMPC)Ccpcz>/Marveld3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Marveld3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472100	M	MP:0003917	increased kidney weight	Marveld3<em1(IMPC)Ccpcz>/Marveld3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Marveld3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472100	F	MP:0000274	enlarged heart	Marveld3<em1(IMPC)Ccpcz>/Marveld3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Marveld3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472100	F	MP:0000703	abnormal thymus morphology	Marveld3<em1(IMPC)Ccpcz>/Marveld3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Marveld3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472100	F	MP:0000709	enlarged thymus	Marveld3<em1(IMPC)Ccpcz>/Marveld3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Marveld3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472100	M	MP:0000154	rib fusion	Marveld3<em1(IMPC)Ccpcz>/Marveld3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Marveld3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472101	M	MP:0000702	enlarged lymph nodes	Metrn<em1(IMPC)Mbp>/Metrn<em1(IMPC)Mbp>	C57BL/6NCrl-Metrn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472101	M	MP:0000691	enlarged spleen	Metrn<em1(IMPC)Mbp>/Metrn<em1(IMPC)Mbp>	C57BL/6NCrl-Metrn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472101	M	MP:0000689	abnormal spleen morphology	Metrn<em1(IMPC)Mbp>/Metrn<em1(IMPC)Mbp>	C57BL/6NCrl-Metrn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472101	F	MP:0002060	abnormal skin morphology	Metrn<em1(IMPC)Mbp>/Metrn<em1(IMPC)Mbp>	C57BL/6NCrl-Metrn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472101	M	MP:0000219	increased neutrophil cell number	Metrn<em1(IMPC)Mbp>/Metrn<em1(IMPC)Mbp>	C57BL/6NCrl-Metrn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472102	M	MP:0002981	increased liver weight	Mettl23<em1(IMPC)Hmgu>/Mettl23<em1(IMPC)Hmgu>	C57BL/6NCrl-Mettl23<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472102	F	MP:0004924	abnormal behavior	Mettl23<em1(IMPC)Hmgu>/Mettl23<em1(IMPC)Hmgu>	C57BL/6NCrl-Mettl23<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472102	M	MP:0004952	increased spleen weight	Mettl23<em1(IMPC)Hmgu>/Mettl23<em1(IMPC)Hmgu>	C57BL/6NCrl-Mettl23<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472102	F	MP:0011964	increased total retina thickness	Mettl23<em1(IMPC)Hmgu>/Mettl23<em1(IMPC)Hmgu>	C57BL/6NCrl-Mettl23<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472102	F	MP:0001289	persistence of hyaloid vascular system	Mettl23<em1(IMPC)Hmgu>/Mettl23<em1(IMPC)Hmgu>	C57BL/6NCrl-Mettl23<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472102	M	MP:0002599	increased mean platelet volume	Mettl23<em1(IMPC)Hmgu>/Mettl23<em1(IMPC)Hmgu>	C57BL/6NCrl-Mettl23<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472102	F	MP:0001364	decreased anxiety-related response	Mettl23<em1(IMPC)Hmgu>/Mettl23<em1(IMPC)Hmgu>	C57BL/6NCrl-Mettl23<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472102	M	MP:0000691	enlarged spleen	Mettl23<em1(IMPC)Hmgu>/Mettl23<em1(IMPC)Hmgu>	C57BL/6NCrl-Mettl23<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472102	M	MP:0011896	increased circulating unsaturated transferrin level	Mettl23<em1(IMPC)Hmgu>/Mettl23<em1(IMPC)Hmgu>	C57BL/6NCrl-Mettl23<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472103	M	MP:0000274	enlarged heart	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472103	F	MP:0000160	kyphosis	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472103	F	MP:0002092	abnormal eye morphology	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472103	F	MP:0002060	abnormal skin morphology	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472103	F	MP:0001126	abnormal ovary morphology	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472103	F	MP:0000703	abnormal thymus morphology	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472103	M	MP:0001417	decreased exploration in new environment	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472103	M	MP:0001147	small testis	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472103	F	MP:0009709	hydrometra	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472103	M	MP:0001402	decreased locomotor activity	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472103	F	MP:0004174	abnormal spine curvature	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472103	F	MP:0001120	abnormal uterus morphology	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472103	F	MP:0000709	enlarged thymus	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472103	M	MP:0000266	abnormal heart morphology	Mfng<em1(IMPC)Ccpcz>/Mfng<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mfng<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472105	M	MP:0004599	abnormal vertebral arch morphology	Mir129-2<em1(IMPC)Kmpc>/Mir129-2<em1(IMPC)Kmpc>	C57BL/6NTac-Mir129-2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472105	M	MP:0010025	decreased total body fat amount	Mir129-2<em1(IMPC)Kmpc>/Mir129-2<em1(IMPC)Kmpc>	C57BL/6NTac-Mir129-2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472105	M	MP:0002833	increased heart weight	Mir129-2<em1(IMPC)Kmpc>/Mir129-2<em1(IMPC)Kmpc>	C57BL/6NTac-Mir129-2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472105	F	MP:0010024	increased total body fat amount	Mir129-2<em1(IMPC)Kmpc>/Mir129-2<em1(IMPC)Kmpc>	C57BL/6NTac-Mir129-2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472105	F	MP:0010053	decreased grip strength	Mir129-2<em1(IMPC)Kmpc>/Mir129-2<em1(IMPC)Kmpc>	C57BL/6NTac-Mir129-2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472105	F	MP:0005293	impaired glucose tolerance	Mir129-2<em1(IMPC)Kmpc>/Mir129-2<em1(IMPC)Kmpc>	C57BL/6NTac-Mir129-2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472105	F	MP:0010124	decreased bone mineral content	Mir129-2<em1(IMPC)Kmpc>/Mir129-2<em1(IMPC)Kmpc>	C57BL/6NTac-Mir129-2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472105	F	MP:0005567	decreased circulating total protein level	Mir129-2<em1(IMPC)Kmpc>/Mir129-2<em1(IMPC)Kmpc>	C57BL/6NTac-Mir129-2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472105	M	MP:0002075	abnormal coat/hair pigmentation	Mir129-2<em1(IMPC)Kmpc>/Mir129-2<em1(IMPC)Kmpc>	C57BL/6NTac-Mir129-2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472105	M	MP:0004174	abnormal spine curvature	Mir129-2<em1(IMPC)Kmpc>/Mir129-2<em1(IMPC)Kmpc>	C57BL/6NTac-Mir129-2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472105	F	MP:0003961	decreased lean body mass	Mir129-2<em1(IMPC)Kmpc>/Mir129-2<em1(IMPC)Kmpc>	C57BL/6NTac-Mir129-2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472109	M	MP:0004952	increased spleen weight	Mri1<em1(IMPC)Bay>/Mri1<em1(IMPC)Bay>	C57BL/6N-Mri1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472110	M	MP:0001297	microphthalmia	Ms4a4a<em1(IMPC)Mbp>/Ms4a4a<em1(IMPC)Mbp>	C57BL/6NCrl-Ms4a4a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472110	M	MP:0002092	abnormal eye morphology	Ms4a4a<em1(IMPC)Mbp>/Ms4a4a<em1(IMPC)Mbp>	C57BL/6NCrl-Ms4a4a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472110	M	MP:0009453	enhanced contextual conditioning behavior	Ms4a4a<em1(IMPC)Mbp>/Ms4a4a<em1(IMPC)Mbp>	C57BL/6NCrl-Ms4a4a<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472111	M	MP:0001556	increased circulating HDL cholesterol level	Ms4a4d<em1(IMPC)J>/Ms4a4d<em1(IMPC)J>	C57BL/6NJ-Ms4a4d<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472111	M	MP:0005178	increased circulating cholesterol level	Ms4a4d<em1(IMPC)J>/Ms4a4d<em1(IMPC)J>	C57BL/6NJ-Ms4a4d<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472112	M	MP:0000218	increased leukocyte cell number	Mxd4<em1(IMPC)J>/Mxd4<em1(IMPC)J>	C57BL/6NJ-Mxd4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472112	F	MP:0000194	increased circulating calcium level	Mxd4<em1(IMPC)J>/Mxd4<em1(IMPC)J>	C57BL/6NJ-Mxd4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472112	F	MP:0010392	prolonged QRS complex duration	Mxd4<em1(IMPC)J>/Mxd4<em1(IMPC)J>	C57BL/6NJ-Mxd4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472113	F	MP:0002092	abnormal eye morphology	Mycbp2<em1(IMPC)Mbp>/Mycbp2<+>	C57BL/6N-Mybpc2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:7472113	M	MP:0000274	enlarged heart	Mycbp2<em1(IMPC)Mbp>/Mycbp2<+>	C57BL/6N-Mybpc2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:7472113	M	MP:0000266	abnormal heart morphology	Mycbp2<em1(IMPC)Mbp>/Mycbp2<+>	C57BL/6N-Mybpc2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:7472113	F	MP:0001293	anophthalmia	Mycbp2<em1(IMPC)Mbp>/Mycbp2<+>	C57BL/6N-Mybpc2<em1(IMPC)Mbp>/Ucd	N	MGI:5576271
MGI:7472115	F	MP:0001258	decreased body length	Myc<em1(IMPC)Kmpc>/Myc<+>	C57BL/6NTac-Myc<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472115	F	MP:0002764	short tibia	Myc<em1(IMPC)Kmpc>/Myc<+>	C57BL/6NTac-Myc<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472115	M	MP:0010052	increased grip strength	Myc<em1(IMPC)Kmpc>/Myc<+>	C57BL/6NTac-Myc<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472115	F	MP:0010124	decreased bone mineral content	Myc<em1(IMPC)Kmpc>/Myc<+>	C57BL/6NTac-Myc<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472117	F	MP:0011960	abnormal eye anterior chamber depth	Myo1a<em1(IMPC)Bay>/Myo1a<em1(IMPC)Bay>	C57BL/6N-Myo1a<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472117	F	MP:0011962	increased cornea thickness	Myo1a<em1(IMPC)Bay>/Myo1a<em1(IMPC)Bay>	C57BL/6N-Myo1a<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472118	M	MP:0001147	small testis	Myo1g<em1(IMPC)Ccpcz>/Myo1g<em1(IMPC)Ccpcz>	C57BL/6NCrl-Myo1g<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472118	M	MP:0003917	increased kidney weight	Myo1g<em1(IMPC)Ccpcz>/Myo1g<em1(IMPC)Ccpcz>	C57BL/6NCrl-Myo1g<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472118	F	MP:0005562	decreased mean corpuscular hemoglobin	Myo1g<em1(IMPC)Ccpcz>/Myo1g<em1(IMPC)Ccpcz>	C57BL/6NCrl-Myo1g<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472118	M	MP:0001146	abnormal testis morphology	Myo1g<em1(IMPC)Ccpcz>/Myo1g<em1(IMPC)Ccpcz>	C57BL/6NCrl-Myo1g<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472121	M	MP:0005333	decreased heart rate	Ndufa7<em1(IMPC)Bay>/Ndufa7<em1(IMPC)Bay>	C57BL/6N-Ndufa7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472121	M	MP:0010506	prolonged RR interval	Ndufa7<em1(IMPC)Bay>/Ndufa7<em1(IMPC)Bay>	C57BL/6N-Ndufa7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472123	M	MP:0001700	abnormal embryo turning	Ndufb5<em1(IMPC)Bay>/Ndufb5<em1(IMPC)Bay>	C57BL/6N-Ndufb5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472123	M	MP:0003864	abnormal midbrain development	Ndufb5<em1(IMPC)Bay>/Ndufb5<em1(IMPC)Bay>	C57BL/6N-Ndufb5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472123	M	MP:0002151	abnormal neural tube morphology	Ndufb5<em1(IMPC)Bay>/Ndufb5<em1(IMPC)Bay>	C57BL/6N-Ndufb5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472123	M	MP:0003720	abnormal neural tube closure	Ndufb5<em1(IMPC)Bay>/Ndufb5<em1(IMPC)Bay>	C57BL/6N-Ndufb5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472123	M	MP:0000269	abnormal heart looping	Ndufb5<em1(IMPC)Bay>/Ndufb5<em1(IMPC)Bay>	C57BL/6N-Ndufb5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472123	M	MP:0002861	abnormal tail bud morphology	Ndufb5<em1(IMPC)Bay>/Ndufb5<em1(IMPC)Bay>	C57BL/6N-Ndufb5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472123	M	MP:0001697	abnormal embryo size	Ndufb5<em1(IMPC)Bay>/Ndufb5<em1(IMPC)Bay>	C57BL/6N-Ndufb5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472123	M	MP:0003232	abnormal forebrain development	Ndufb5<em1(IMPC)Bay>/Ndufb5<em1(IMPC)Bay>	C57BL/6N-Ndufb5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472123	M	MP:0000266	abnormal heart morphology	Ndufb5<em1(IMPC)Bay>/Ndufb5<em1(IMPC)Bay>	C57BL/6N-Ndufb5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472123	M	MP:0001726	abnormal allantois morphology	Ndufb5<em1(IMPC)Bay>/Ndufb5<em1(IMPC)Bay>	C57BL/6N-Ndufb5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472123	M	MP:0003984	embryonic growth retardation	Ndufb5<em1(IMPC)Bay>/Ndufb5<em1(IMPC)Bay>	C57BL/6N-Ndufb5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472124	M	MP:0002574	increased vertical activity	Ndufs5<em1(IMPC)Bay>/Ndufs5<+>	C57BL/6N-Ndufs5<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472126	F	MP:0004924	abnormal behavior	Ndufv3<em1(IMPC)Bay>/Ndufv3<em1(IMPC)Bay>	C57BL/6N-Ndufv3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472126	F	MP:0001402	decreased locomotor activity	Ndufv3<em1(IMPC)Bay>/Ndufv3<em1(IMPC)Bay>	C57BL/6N-Ndufv3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472126	F	MP:0020870	decreased thigmotaxis	Ndufv3<em1(IMPC)Bay>/Ndufv3<em1(IMPC)Bay>	C57BL/6N-Ndufv3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472127	M	MP:0011971	increased circulating lactate dehydrogenase level	Nfe2l2<em1(IMPC)Ccpcz>/Nfe2l2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nfe2l2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472127	F	MP:0005344	increased circulating bilirubin level	Nfe2l2<em1(IMPC)Ccpcz>/Nfe2l2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nfe2l2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472127	M	MP:0002059	abnormal seminal vesicle morphology	Nfe2l2<em1(IMPC)Ccpcz>/Nfe2l2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nfe2l2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472127	F	MP:0000703	abnormal thymus morphology	Nfe2l2<em1(IMPC)Ccpcz>/Nfe2l2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nfe2l2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472127	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Nfe2l2<em1(IMPC)Ccpcz>/Nfe2l2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nfe2l2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472127	F	MP:0002100	abnormal tooth morphology	Nfe2l2<em1(IMPC)Ccpcz>/Nfe2l2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nfe2l2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472127	M	MP:0002997	enlarged seminal vesicle	Nfe2l2<em1(IMPC)Ccpcz>/Nfe2l2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nfe2l2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472127	F	MP:0000709	enlarged thymus	Nfe2l2<em1(IMPC)Ccpcz>/Nfe2l2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nfe2l2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472127	F	MP:0005560	decreased circulating glucose level	Nfe2l2<em1(IMPC)Ccpcz>/Nfe2l2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nfe2l2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472127	F	MP:0000702	enlarged lymph nodes	Nfe2l2<em1(IMPC)Ccpcz>/Nfe2l2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nfe2l2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472127	M	MP:0002599	increased mean platelet volume	Nfe2l2<em1(IMPC)Ccpcz>/Nfe2l2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nfe2l2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472127	F	MP:0001126	abnormal ovary morphology	Nfe2l2<em1(IMPC)Ccpcz>/Nfe2l2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nfe2l2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472128	M	MP:0002606	increased basophil cell number	Nherf1<em1(IMPC)H>/Nherf1<em1(IMPC)H>	C57BL/6NTac-Nherf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472128	M	MP:0004151	decreased circulating iron level	Nherf1<em1(IMPC)H>/Nherf1<em1(IMPC)H>	C57BL/6NTac-Nherf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472128	M	MP:0000218	increased leukocyte cell number	Nherf1<em1(IMPC)H>/Nherf1<em1(IMPC)H>	C57BL/6NTac-Nherf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472129	F	MP:0001926	female infertility	Nlrp14<em1(IMPC)Bay>/Nlrp14<em1(IMPC)Bay>	C57BL/6N-Nlrp14<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472130	M	MP:0001417	decreased exploration in new environment	Nono<em1(IMPC)Bay>/Y	C57BL/6N-Nono<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472131	F	MP:0001417	decreased exploration in new environment	Nono<em1(IMPC)Bay>/Nono<em1(IMPC)Bay>	C57BL/6N-Nono<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472132	M	MP:0000598	abnormal liver morphology	Nrsn2<em1(IMPC)Kmpc>/Nrsn2<em1(IMPC)Kmpc>	C57BL/6NTac-Nrsn2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472132	F	MP:0001566	increased circulating phosphate level	Nrsn2<em1(IMPC)Kmpc>/Nrsn2<em1(IMPC)Kmpc>	C57BL/6NTac-Nrsn2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472132	F	MP:0008821	increased blood uric acid level	Nrsn2<em1(IMPC)Kmpc>/Nrsn2<em1(IMPC)Kmpc>	C57BL/6NTac-Nrsn2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472132	F	MP:0010067	increased red blood cell distribution width	Nrsn2<em1(IMPC)Kmpc>/Nrsn2<em1(IMPC)Kmpc>	C57BL/6NTac-Nrsn2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472132	F	MP:0000194	increased circulating calcium level	Nrsn2<em1(IMPC)Kmpc>/Nrsn2<em1(IMPC)Kmpc>	C57BL/6NTac-Nrsn2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472132	F	MP:0002339	abnormal lymph node morphology	Nrsn2<em1(IMPC)Kmpc>/Nrsn2<em1(IMPC)Kmpc>	C57BL/6NTac-Nrsn2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472133	F	MP:0002965	increased circulating serum albumin level	Nsg2<em1(IMPC)Kmpc>/Nsg2<em1(IMPC)Kmpc>	C57BL/6NTac-Nsg2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472133	F	MP:0009455	enhanced cued conditioning behavior	Nsg2<em1(IMPC)Kmpc>/Nsg2<em1(IMPC)Kmpc>	C57BL/6NTac-Nsg2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472136	F	MP:0000367	abnormal coat/ hair morphology	Nxnl2<em1(IMPC)Ccpcz>/Nxnl2<+>	C57BL/6NCrl-Nxnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472136	M	MP:0000703	abnormal thymus morphology	Nxnl2<em1(IMPC)Ccpcz>/Nxnl2<+>	C57BL/6NCrl-Nxnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472136	M	MP:0000691	enlarged spleen	Nxnl2<em1(IMPC)Ccpcz>/Nxnl2<+>	C57BL/6NCrl-Nxnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472136	M	MP:0000689	abnormal spleen morphology	Nxnl2<em1(IMPC)Ccpcz>/Nxnl2<+>	C57BL/6NCrl-Nxnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472136	M	MP:0000709	enlarged thymus	Nxnl2<em1(IMPC)Ccpcz>/Nxnl2<+>	C57BL/6NCrl-Nxnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472137	F	MP:0000709	enlarged thymus	Nxnl2<em1(IMPC)Ccpcz>/Nxnl2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nxnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472137	F	MP:0000759	abnormal skeletal muscle morphology	Nxnl2<em1(IMPC)Ccpcz>/Nxnl2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nxnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472137	M	MP:0003961	decreased lean body mass	Nxnl2<em1(IMPC)Ccpcz>/Nxnl2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nxnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472137	F	MP:0000703	abnormal thymus morphology	Nxnl2<em1(IMPC)Ccpcz>/Nxnl2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nxnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472137	F	MP:0000691	enlarged spleen	Nxnl2<em1(IMPC)Ccpcz>/Nxnl2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nxnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472137	F	MP:0000689	abnormal spleen morphology	Nxnl2<em1(IMPC)Ccpcz>/Nxnl2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nxnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472137	M	MP:0000222	decreased neutrophil cell number	Nxnl2<em1(IMPC)Ccpcz>/Nxnl2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nxnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472138	F	MP:0002135	abnormal kidney morphology	Obp2b<em1(IMPC)Kmpc>/Obp2b<em1(IMPC)Kmpc>	C57BL/6NTac-Obp2b<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472138	M	MP:0002059	abnormal seminal vesicle morphology	Obp2b<em1(IMPC)Kmpc>/Obp2b<em1(IMPC)Kmpc>	C57BL/6NTac-Obp2b<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472138	F	MP:0011110	preweaning lethality, incomplete penetrance	Obp2b<em1(IMPC)Kmpc>/Obp2b<em1(IMPC)Kmpc>	C57BL/6NTac-Obp2b<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472138	M	MP:0010506	prolonged RR interval	Obp2b<em1(IMPC)Kmpc>/Obp2b<em1(IMPC)Kmpc>	C57BL/6NTac-Obp2b<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472138	M	MP:0002339	abnormal lymph node morphology	Obp2b<em1(IMPC)Kmpc>/Obp2b<em1(IMPC)Kmpc>	C57BL/6NTac-Obp2b<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472138	M	MP:0000367	abnormal coat/ hair morphology	Obp2b<em1(IMPC)Kmpc>/Obp2b<em1(IMPC)Kmpc>	C57BL/6NTac-Obp2b<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472138	F	MP:0003068	enlarged kidney	Obp2b<em1(IMPC)Kmpc>/Obp2b<em1(IMPC)Kmpc>	C57BL/6NTac-Obp2b<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472139	M	MP:0003917	increased kidney weight	Odaph<em1(IMPC)Ccpcz>/Odaph<em1(IMPC)Ccpcz>	C57BL/6NCrl-Odaph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472139	M	MP:0002968	increased circulating alkaline phosphatase level	Odaph<em1(IMPC)Ccpcz>/Odaph<em1(IMPC)Ccpcz>	C57BL/6NCrl-Odaph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472139	M	MP:0000689	abnormal spleen morphology	Odaph<em1(IMPC)Ccpcz>/Odaph<em1(IMPC)Ccpcz>	C57BL/6NCrl-Odaph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472139	F	MP:0000703	abnormal thymus morphology	Odaph<em1(IMPC)Ccpcz>/Odaph<em1(IMPC)Ccpcz>	C57BL/6NCrl-Odaph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472139	F	MP:0000709	enlarged thymus	Odaph<em1(IMPC)Ccpcz>/Odaph<em1(IMPC)Ccpcz>	C57BL/6NCrl-Odaph<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472140	F	MP:0000709	enlarged thymus	Cimap1b<em1(IMPC)Ccpcz>/Cimap1b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cimap1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472140	M	MP:0000689	abnormal spleen morphology	Cimap1b<em1(IMPC)Ccpcz>/Cimap1b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cimap1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472140	M	MP:0001262	decreased body weight	Cimap1b<em1(IMPC)Ccpcz>/Cimap1b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cimap1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472140	F	MP:0002110	abnormal digit morphology	Cimap1b<em1(IMPC)Ccpcz>/Cimap1b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cimap1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472140	F	MP:0000266	abnormal heart morphology	Cimap1b<em1(IMPC)Ccpcz>/Cimap1b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cimap1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472140	F	MP:0000703	abnormal thymus morphology	Cimap1b<em1(IMPC)Ccpcz>/Cimap1b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cimap1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472140	F	MP:0000274	enlarged heart	Cimap1b<em1(IMPC)Ccpcz>/Cimap1b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cimap1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472140	M	MP:0000691	enlarged spleen	Cimap1b<em1(IMPC)Ccpcz>/Cimap1b<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cimap1b<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472142	M	MP:0013279	increased fasting circulating glucose level	Or5b112<em1(IMPC)Hmgu>/Or5b112<em1(IMPC)Hmgu>	C57BL/6NCrl-Or5b112<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472143	M	MP:0002092	abnormal eye morphology	Or8h8<em1(IMPC)Mbp>/Or8h8<em1(IMPC)Mbp>	C57BL/6NCrl-Or8h8<em1(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:7472145	M	MP:0001262	decreased body weight	Otop1<em1(IMPC)Ccpcz>/Otop1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Otop1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472145	F	MP:0000703	abnormal thymus morphology	Otop1<em1(IMPC)Ccpcz>/Otop1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Otop1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472145	M	MP:0005343	increased circulating aspartate transaminase level	Otop1<em1(IMPC)Ccpcz>/Otop1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Otop1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472145	F	MP:0000689	abnormal spleen morphology	Otop1<em1(IMPC)Ccpcz>/Otop1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Otop1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472145	F	MP:0000709	enlarged thymus	Otop1<em1(IMPC)Ccpcz>/Otop1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Otop1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472146	M	MP:0013129	abnormal tooth color	Pabir2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472146	M	MP:0002100	abnormal tooth morphology	Pabir2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472146	M	MP:0001148	enlarged testis	Pabir2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472146	M	MP:0001147	small testis	Pabir2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472146	M	MP:0000709	enlarged thymus	Pabir2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472146	M	MP:0002691	small stomach	Pabir2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472146	M	MP:0001146	abnormal testis morphology	Pabir2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472146	M	MP:0000470	abnormal stomach morphology	Pabir2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472146	M	MP:0000689	abnormal spleen morphology	Pabir2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472146	M	MP:0000703	abnormal thymus morphology	Pabir2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472146	M	MP:0000692	small spleen	Pabir2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472146	M	MP:0002060	abnormal skin morphology	Pabir2<em1(IMPC)Ccpcz>/Y	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472147	F	MP:0013129	abnormal tooth color	Pabir2<em1(IMPC)Ccpcz>/Pabir2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472147	F	MP:0000691	enlarged spleen	Pabir2<em1(IMPC)Ccpcz>/Pabir2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472147	F	MP:0000266	abnormal heart morphology	Pabir2<em1(IMPC)Ccpcz>/Pabir2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472147	F	MP:0000703	abnormal thymus morphology	Pabir2<em1(IMPC)Ccpcz>/Pabir2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472147	F	MP:0000689	abnormal spleen morphology	Pabir2<em1(IMPC)Ccpcz>/Pabir2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472147	F	MP:0000702	enlarged lymph nodes	Pabir2<em1(IMPC)Ccpcz>/Pabir2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472147	F	MP:0000709	enlarged thymus	Pabir2<em1(IMPC)Ccpcz>/Pabir2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472147	F	MP:0002188	small heart	Pabir2<em1(IMPC)Ccpcz>/Pabir2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472147	F	MP:0002339	abnormal lymph node morphology	Pabir2<em1(IMPC)Ccpcz>/Pabir2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472147	F	MP:0001399	hyperactivity	Pabir2<em1(IMPC)Ccpcz>/Pabir2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472147	F	MP:0002100	abnormal tooth morphology	Pabir2<em1(IMPC)Ccpcz>/Pabir2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pabir2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472148	F	MP:0009455	enhanced cued conditioning behavior	Pald1<em1(IMPC)Kmpc>/Pald1<em1(IMPC)Kmpc>	C57BL/6NTac-Pald1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472148	M	MP:0020421	increased freezing behavior	Pald1<em1(IMPC)Kmpc>/Pald1<em1(IMPC)Kmpc>	C57BL/6NTac-Pald1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472148	F	MP:0002092	abnormal eye morphology	Pald1<em1(IMPC)Kmpc>/Pald1<em1(IMPC)Kmpc>	C57BL/6NTac-Pald1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472149	M	MP:0005554	decreased circulating creatinine level	Pank4<em1(IMPC)Kmpc>/Pank4<em1(IMPC)Kmpc>	C57BL/6NTac-Pank4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472149	F	MP:0001399	hyperactivity	Pank4<em1(IMPC)Kmpc>/Pank4<em1(IMPC)Kmpc>	C57BL/6NTac-Pank4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472149	M	MP:0000598	abnormal liver morphology	Pank4<em1(IMPC)Kmpc>/Pank4<em1(IMPC)Kmpc>	C57BL/6NTac-Pank4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472149	M	MP:0020421	increased freezing behavior	Pank4<em1(IMPC)Kmpc>/Pank4<em1(IMPC)Kmpc>	C57BL/6NTac-Pank4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472152	F	MP:0002100	abnormal tooth morphology	Parva<em1(IMPC)Ccpcz>/Parva<+>	C57BL/6NCrl-Parva<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472152	F	MP:0000691	enlarged spleen	Parva<em1(IMPC)Ccpcz>/Parva<+>	C57BL/6NCrl-Parva<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472152	F	MP:0000274	enlarged heart	Parva<em1(IMPC)Ccpcz>/Parva<+>	C57BL/6NCrl-Parva<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472152	F	MP:0000266	abnormal heart morphology	Parva<em1(IMPC)Ccpcz>/Parva<+>	C57BL/6NCrl-Parva<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472152	F	MP:0000689	abnormal spleen morphology	Parva<em1(IMPC)Ccpcz>/Parva<+>	C57BL/6NCrl-Parva<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472152	F	MP:0001126	abnormal ovary morphology	Parva<em1(IMPC)Ccpcz>/Parva<+>	C57BL/6NCrl-Parva<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472156	F	MP:0001303	abnormal lens morphology	Pcdh12<em2(IMPC)J>/Pcdh12<em2(IMPC)J>	C57BL/6NJ-Pcdh12<em1(IMPC)J>/J	N	MGI:5576271
MGI:7472160	F	MP:0001944	abnormal pancreas morphology	Pdlim4<em1(IMPC)Ics>/Pdlim4<em1(IMPC)Ics>	C57BL/6N-Pdlim4<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:7472160	F	MP:0002764	short tibia	Pdlim4<em1(IMPC)Ics>/Pdlim4<em1(IMPC)Ics>	C57BL/6N-Pdlim4<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:7472160	F	MP:0005292	improved glucose tolerance	Pdlim4<em1(IMPC)Ics>/Pdlim4<em1(IMPC)Ics>	C57BL/6N-Pdlim4<em2(IMPC)Ics>/Ics	N	MGI:5576271
MGI:7472161	F	MP:0003960	increased lean body mass	Peli3<tm1a(KOMP)Mbp>/Peli3<tm1a(KOMP)Mbp>	C57BL/6NTac-Peli3<tm1a(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:7472161	F	MP:0010123	increased bone mineral content	Peli3<tm1a(KOMP)Mbp>/Peli3<tm1a(KOMP)Mbp>	C57BL/6NTac-Peli3<tm1a(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:7472161	F	MP:0010025	decreased total body fat amount	Peli3<tm1a(KOMP)Mbp>/Peli3<tm1a(KOMP)Mbp>	C57BL/6NTac-Peli3<tm1a(KOMP)Mbp>/Kmpc	N	MGI:5576271
MGI:7472163	M	MP:0001146	abnormal testis morphology	Pgap6<em1(IMPC)Mbp>/Pgap6<+>	C57BL/6NCrl-Pgap6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472163	F	MP:0002060	abnormal skin morphology	Pgap6<em1(IMPC)Mbp>/Pgap6<+>	C57BL/6NCrl-Pgap6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472163	M	MP:0001147	small testis	Pgap6<em1(IMPC)Mbp>/Pgap6<+>	C57BL/6NCrl-Pgap6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472164	M	MP:0001925	male infertility	Pgap6<em1(IMPC)Mbp>/Pgap6<em1(IMPC)Mbp>	C57BL/6NCrl-Pgap6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472166	M	MP:0010068	decreased red blood cell distribution width	Phb1<em1(IMPC)H>/Phb1<+>	C57BL/6NTac-Phb1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472168	M	MP:0005292	improved glucose tolerance	Phf8<tm1dIcs>/Y	C57BL/6N-Phf8<tm1dIcs>/Ics	N	MGI:5576271
MGI:7472168	M	MP:0001556	increased circulating HDL cholesterol level	Phf8<tm1dIcs>/Y	C57BL/6N-Phf8<tm1dIcs>/Ics	N	MGI:5576271
MGI:7472168	M	MP:0011960	abnormal eye anterior chamber depth	Phf8<tm1dIcs>/Y	C57BL/6N-Phf8<tm1dIcs>/Ics	N	MGI:5576271
MGI:7472169	F	MP:0011960	abnormal eye anterior chamber depth	Phf8<tm1dIcs>/Phf8<tm1dIcs>	C57BL/6N-Phf8<tm1dIcs>/Ics	N	MGI:5576271
MGI:7472169	F	MP:0001556	increased circulating HDL cholesterol level	Phf8<tm1dIcs>/Phf8<tm1dIcs>	C57BL/6N-Phf8<tm1dIcs>/Ics	N	MGI:5576271
MGI:7472169	F	MP:0003921	abnormal heart left ventricle morphology	Phf8<tm1dIcs>/Phf8<tm1dIcs>	C57BL/6N-Phf8<tm1dIcs>/Ics	N	MGI:5576271
MGI:7472169	F	MP:0000219	increased neutrophil cell number	Phf8<tm1dIcs>/Phf8<tm1dIcs>	C57BL/6N-Phf8<tm1dIcs>/Ics	N	MGI:5576271
MGI:7472169	F	MP:0005016	decreased lymphocyte cell number	Phf8<tm1dIcs>/Phf8<tm1dIcs>	C57BL/6N-Phf8<tm1dIcs>/Ics	N	MGI:5576271
MGI:7472169	F	MP:0002941	increased circulating alanine transaminase level	Phf8<tm1dIcs>/Phf8<tm1dIcs>	C57BL/6N-Phf8<tm1dIcs>/Ics	N	MGI:5576271
MGI:7472171	F	MP:0002968	increased circulating alkaline phosphatase level	Pitpnc1<em1(IMPC)Kmpc>/Pitpnc1<em1(IMPC)Kmpc>	C57BL/6NTac-Pitpnc1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472171	F	MP:0005560	decreased circulating glucose level	Pitpnc1<em1(IMPC)Kmpc>/Pitpnc1<em1(IMPC)Kmpc>	C57BL/6NTac-Pitpnc1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472171	M	MP:0003960	increased lean body mass	Pitpnc1<em1(IMPC)Kmpc>/Pitpnc1<em1(IMPC)Kmpc>	C57BL/6NTac-Pitpnc1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472171	F	MP:0002965	increased circulating serum albumin level	Pitpnc1<em1(IMPC)Kmpc>/Pitpnc1<em1(IMPC)Kmpc>	C57BL/6NTac-Pitpnc1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472171	M	MP:0010090	increased circulating creatine kinase level	Pitpnc1<em1(IMPC)Kmpc>/Pitpnc1<em1(IMPC)Kmpc>	C57BL/6NTac-Pitpnc1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472171	M	MP:0005292	improved glucose tolerance	Pitpnc1<em1(IMPC)Kmpc>/Pitpnc1<em1(IMPC)Kmpc>	C57BL/6NTac-Pitpnc1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472171	F	MP:0000062	increased bone mineral density	Pitpnc1<em1(IMPC)Kmpc>/Pitpnc1<em1(IMPC)Kmpc>	C57BL/6NTac-Pitpnc1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472172	M	MP:0002968	increased circulating alkaline phosphatase level	Plekhf2<em1(IMPC)Wtsi>/Plekhf2<em1(IMPC)Wtsi>	C57BL/6NCrl-Plekhf2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:7472172	M	MP:0002989	small kidney	Plekhf2<em1(IMPC)Wtsi>/Plekhf2<em1(IMPC)Wtsi>	C57BL/6NCrl-Plekhf2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:7472172	M	MP:0001489	decreased startle reflex	Plekhf2<em1(IMPC)Wtsi>/Plekhf2<em1(IMPC)Wtsi>	C57BL/6NCrl-Plekhf2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:7472174	F	MP:0020870	decreased thigmotaxis	Plin4<tm1.1(KOMP)Wtsi>/Plin4<tm1.1(KOMP)Wtsi>	C57BL/6N-Plin4<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:7472174	F	MP:0004924	abnormal behavior	Plin4<tm1.1(KOMP)Wtsi>/Plin4<tm1.1(KOMP)Wtsi>	C57BL/6N-Plin4<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:7472174	M	MP:0001258	decreased body length	Plin4<tm1.1(KOMP)Wtsi>/Plin4<tm1.1(KOMP)Wtsi>	C57BL/6N-Plin4<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:7472174	M	MP:0000598	abnormal liver morphology	Plin4<tm1.1(KOMP)Wtsi>/Plin4<tm1.1(KOMP)Wtsi>	C57BL/6N-Plin4<tm1.1(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:7472175	F	MP:0000709	enlarged thymus	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472175	F	MP:0000703	abnormal thymus morphology	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472175	F	MP:0002339	abnormal lymph node morphology	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472175	M	MP:0003917	increased kidney weight	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472175	M	MP:0011625	cystolithiasis	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472175	F	MP:0000702	enlarged lymph nodes	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472175	M	MP:0002059	abnormal seminal vesicle morphology	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472175	M	MP:0000274	enlarged heart	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472175	M	MP:0001147	small testis	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472175	M	MP:0003795	abnormal bone structure	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472175	M	MP:0001146	abnormal testis morphology	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472175	M	MP:0000266	abnormal heart morphology	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472175	M	MP:0000538	abnormal urinary bladder morphology	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472175	F	MP:0001293	anophthalmia	Plppr5<em1(IMPC)Ccpcz>/Plppr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Plppr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472176	F	MP:0002135	abnormal kidney morphology	Pnkp<em1(IMPC)Mbp>/Pnkp<+>	C57BL/6NCrl-Pnkp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472176	F	MP:0001297	microphthalmia	Pnkp<em1(IMPC)Mbp>/Pnkp<+>	C57BL/6NCrl-Pnkp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472176	F	MP:0003604	single kidney	Pnkp<em1(IMPC)Mbp>/Pnkp<+>	C57BL/6NCrl-Pnkp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472176	F	MP:0003068	enlarged kidney	Pnkp<em1(IMPC)Mbp>/Pnkp<+>	C57BL/6NCrl-Pnkp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472176	F	MP:0002092	abnormal eye morphology	Pnkp<em1(IMPC)Mbp>/Pnkp<+>	C57BL/6NCrl-Pnkp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472176	F	MP:0002060	abnormal skin morphology	Pnkp<em1(IMPC)Mbp>/Pnkp<+>	C57BL/6NCrl-Pnkp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472178	M	MP:0002135	abnormal kidney morphology	Pomk<em1(IMPC)Hmgu>/Pomk<+>	C57BL/6NCrl-Pomk<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472178	F	MP:0004952	increased spleen weight	Pomk<em1(IMPC)Hmgu>/Pomk<+>	C57BL/6NCrl-Pomk<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472178	M	MP:0000062	increased bone mineral density	Pomk<em1(IMPC)Hmgu>/Pomk<+>	C57BL/6NCrl-Pomk<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472180	F	MP:0000219	increased neutrophil cell number	Ppp1r17<em1(IMPC)H>/Ppp1r17<em1(IMPC)H>	C57BL/6NTac-Ppp1r17<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472182	M	MP:0001147	small testis	Pramel13<em1(IMPC)Mbp>/Pramel13<em1(IMPC)Mbp>	C57BL/6NCrl-Pramel13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472182	M	MP:0001146	abnormal testis morphology	Pramel13<em1(IMPC)Mbp>/Pramel13<em1(IMPC)Mbp>	C57BL/6NCrl-Pramel13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472182	M	MP:0001925	male infertility	Pramel13<em1(IMPC)Mbp>/Pramel13<em1(IMPC)Mbp>	C57BL/6NCrl-Pramel13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472182	M	MP:0002060	abnormal skin morphology	Pramel13<em1(IMPC)Mbp>/Pramel13<em1(IMPC)Mbp>	C57BL/6NCrl-Pramel13<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472183	F	MP:0002953	thick ventricular wall	Prpf8<em1(IMPC)Bay>/Prpf8<+>	C57BL/6N-Prpf8<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472184	M	MP:0002059	abnormal seminal vesicle morphology	Prrg4<em1(IMPC)Mbp>/Prrg4<em1(IMPC)Mbp>	C57BL/6NCrl-Prrg4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472184	M	MP:0000689	abnormal spleen morphology	Prrg4<em1(IMPC)Mbp>/Prrg4<em1(IMPC)Mbp>	C57BL/6NCrl-Prrg4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472184	M	MP:0001157	small seminal vesicle	Prrg4<em1(IMPC)Mbp>/Prrg4<em1(IMPC)Mbp>	C57BL/6NCrl-Prrg4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472184	M	MP:0000691	enlarged spleen	Prrg4<em1(IMPC)Mbp>/Prrg4<em1(IMPC)Mbp>	C57BL/6NCrl-Prrg4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472186	M	MP:0000266	abnormal heart morphology	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472186	M	MP:0002060	abnormal skin morphology	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472186	M	MP:0001146	abnormal testis morphology	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472186	M	MP:0000495	abnormal colon morphology	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472186	F	MP:0000709	enlarged thymus	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472186	F	MP:0000703	abnormal thymus morphology	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472186	F	MP:0013763	increased T-helper cell number	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472186	F	MP:0013771	decreased effector memory T-helper cell number	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472186	M	MP:0000274	enlarged heart	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472186	M	MP:0001147	small testis	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472186	F	MP:0013772	increased effector memory T-helper cell number	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472186	F	MP:0008074	increased CD4-positive, alpha-beta T cell number	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472186	M	MP:0003917	increased kidney weight	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472186	M	MP:0002581	abnormal ileum morphology	Psmb11<em1(IMPC)Ccpcz>/Psmb11<em1(IMPC)Ccpcz>	C57BL/6NCrl-Psmb11<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472187	M	MP:0005333	decreased heart rate	Psors1c2<em1(IMPC)Hmgu>/Psors1c2<+>	C57BL/6NCrl-Psors1c2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472187	M	MP:0010506	prolonged RR interval	Psors1c2<em1(IMPC)Hmgu>/Psors1c2<+>	C57BL/6NCrl-Psors1c2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472189	F	MP:0000494	abnormal cecum morphology	Ptgs1<em1(IMPC)Mbp>/Ptgs1<em1(IMPC)Mbp>	C57BL/6NCrl-Ptgs1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472189	F	MP:0009476	enlarged cecum	Ptgs1<em1(IMPC)Mbp>/Ptgs1<em1(IMPC)Mbp>	C57BL/6NCrl-Ptgs1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472192	F	MP:0002152	abnormal brain morphology	Qars1<em1(IMPC)Mbp>/Qars1<+>	C57BL/6NCrl-Qars1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472192	F	MP:0001293	anophthalmia	Qars1<em1(IMPC)Mbp>/Qars1<+>	C57BL/6NCrl-Qars1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472192	M	MP:0001289	persistence of hyaloid vascular system	Qars1<em1(IMPC)Mbp>/Qars1<+>	C57BL/6NCrl-Qars1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472192	F	MP:0000759	abnormal skeletal muscle morphology	Qars1<em1(IMPC)Mbp>/Qars1<+>	C57BL/6NCrl-Qars1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472192	F	MP:0002060	abnormal skin morphology	Qars1<em1(IMPC)Mbp>/Qars1<+>	C57BL/6NCrl-Qars1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472194	M	MP:0002075	abnormal coat/hair pigmentation	Qsox1<em1(IMPC)Kmpc>/Qsox1<em1(IMPC)Kmpc>	C57BL/6NTac-Qsox1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472194	F	MP:0009142	decreased prepulse inhibition	Qsox1<em1(IMPC)Kmpc>/Qsox1<em1(IMPC)Kmpc>	C57BL/6NTac-Qsox1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472194	M	MP:0011971	increased circulating lactate dehydrogenase level	Qsox1<em1(IMPC)Kmpc>/Qsox1<em1(IMPC)Kmpc>	C57BL/6NTac-Qsox1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472194	F	MP:0002833	increased heart weight	Qsox1<em1(IMPC)Kmpc>/Qsox1<em1(IMPC)Kmpc>	C57BL/6NTac-Qsox1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472194	F	MP:0010052	increased grip strength	Qsox1<em1(IMPC)Kmpc>/Qsox1<em1(IMPC)Kmpc>	C57BL/6NTac-Qsox1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472199	F	MP:0002135	abnormal kidney morphology	Rbm10<em1(IMPC)Mbp>/Rbm10<+>	C57BL/6NCrl-Rbm10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472199	F	MP:0001304	cataract	Rbm10<em1(IMPC)Mbp>/Rbm10<+>	C57BL/6NCrl-Rbm10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472199	F	MP:0000689	abnormal spleen morphology	Rbm10<em1(IMPC)Mbp>/Rbm10<+>	C57BL/6NCrl-Rbm10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472199	F	MP:0000691	enlarged spleen	Rbm10<em1(IMPC)Mbp>/Rbm10<+>	C57BL/6NCrl-Rbm10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472199	F	MP:0009084	blind uterus	Rbm10<em1(IMPC)Mbp>/Rbm10<+>	C57BL/6NCrl-Rbm10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472199	F	MP:0002699	abnormal vitreous body morphology	Rbm10<em1(IMPC)Mbp>/Rbm10<+>	C57BL/6NCrl-Rbm10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472199	F	MP:0000598	abnormal liver morphology	Rbm10<em1(IMPC)Mbp>/Rbm10<+>	C57BL/6NCrl-Rbm10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472199	F	MP:0002989	small kidney	Rbm10<em1(IMPC)Mbp>/Rbm10<+>	C57BL/6NCrl-Rbm10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472199	F	MP:0000601	small liver	Rbm10<em1(IMPC)Mbp>/Rbm10<+>	C57BL/6NCrl-Rbm10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472199	F	MP:0002092	abnormal eye morphology	Rbm10<em1(IMPC)Mbp>/Rbm10<+>	C57BL/6NCrl-Rbm10<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472200	F	MP:0005344	increased circulating bilirubin level	Reg3b<em1(IMPC)Mbp>/Reg3b<em1(IMPC)Mbp>	C57BL/6NCrl-Reg3b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472200	F	MP:0000601	small liver	Reg3b<em1(IMPC)Mbp>/Reg3b<em1(IMPC)Mbp>	C57BL/6NCrl-Reg3b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472200	F	MP:0000598	abnormal liver morphology	Reg3b<em1(IMPC)Mbp>/Reg3b<em1(IMPC)Mbp>	C57BL/6NCrl-Reg3b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472200	F	MP:0000689	abnormal spleen morphology	Reg3b<em1(IMPC)Mbp>/Reg3b<em1(IMPC)Mbp>	C57BL/6NCrl-Reg3b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472200	M	MP:0001146	abnormal testis morphology	Reg3b<em1(IMPC)Mbp>/Reg3b<em1(IMPC)Mbp>	C57BL/6NCrl-Reg3b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472200	M	MP:0001148	enlarged testis	Reg3b<em1(IMPC)Mbp>/Reg3b<em1(IMPC)Mbp>	C57BL/6NCrl-Reg3b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472200	F	MP:0000691	enlarged spleen	Reg3b<em1(IMPC)Mbp>/Reg3b<em1(IMPC)Mbp>	C57BL/6NCrl-Reg3b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472201	M	MP:0002874	decreased hemoglobin content	Reg4<tm1b(EUCOMM)Hmgu>/Reg4<tm1b(EUCOMM)Hmgu>	C57BL/6NTac-Reg4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:7472201	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Reg4<tm1b(EUCOMM)Hmgu>/Reg4<tm1b(EUCOMM)Hmgu>	C57BL/6NTac-Reg4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:7472201	M	MP:0005562	decreased mean corpuscular hemoglobin	Reg4<tm1b(EUCOMM)Hmgu>/Reg4<tm1b(EUCOMM)Hmgu>	C57BL/6NTac-Reg4<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:7472202	M	MP:0005568	increased circulating total protein level	Rhag<em1(IMPC)Ccpcz>/Rhag<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rhag<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472202	M	MP:0000266	abnormal heart morphology	Rhag<em1(IMPC)Ccpcz>/Rhag<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rhag<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472202	M	MP:0001146	abnormal testis morphology	Rhag<em1(IMPC)Ccpcz>/Rhag<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rhag<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472202	F	MP:0002339	abnormal lymph node morphology	Rhag<em1(IMPC)Ccpcz>/Rhag<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rhag<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472202	F	MP:0000703	abnormal thymus morphology	Rhag<em1(IMPC)Ccpcz>/Rhag<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rhag<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472202	M	MP:0000274	enlarged heart	Rhag<em1(IMPC)Ccpcz>/Rhag<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rhag<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472202	F	MP:0000702	enlarged lymph nodes	Rhag<em1(IMPC)Ccpcz>/Rhag<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rhag<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472202	F	MP:0000709	enlarged thymus	Rhag<em1(IMPC)Ccpcz>/Rhag<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rhag<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472202	M	MP:0001147	small testis	Rhag<em1(IMPC)Ccpcz>/Rhag<em1(IMPC)Ccpcz>	C57BL/6NCrl-Rhag<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472203	M	MP:0001417	decreased exploration in new environment	Rin2<em1(IMPC)Bay>/Rin2<em1(IMPC)Bay>	C57BL/6N-Rin2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472204	F	MP:0001293	anophthalmia	Riok3<em1(IMPC)Mbp>/Riok3<em1(IMPC)Mbp>	C57BL/6NCrl-Riok3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472204	F	MP:0001289	persistence of hyaloid vascular system	Riok3<em1(IMPC)Mbp>/Riok3<em1(IMPC)Mbp>	C57BL/6NCrl-Riok3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472204	M	MP:0001925	male infertility	Riok3<em1(IMPC)Mbp>/Riok3<em1(IMPC)Mbp>	C57BL/6NCrl-Riok3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472204	F	MP:0002092	abnormal eye morphology	Riok3<em1(IMPC)Mbp>/Riok3<em1(IMPC)Mbp>	C57BL/6NCrl-Riok3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472205	F	MP:0005632	decreased circulating aspartate transaminase level	Rnf126<em1(IMPC)J>/Rnf126<+>	C57BL/6NJ-Rnf126<em1(IMPC)J>/J	N	MGI:5576271
MGI:7472206	F	MP:0001488	increased startle reflex	Rnf166<em1(IMPC)J>/Rnf166<em1(IMPC)J>	C57BL/6NJ-Rnf166<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472206	F	MP:0000198	decreased circulating phosphate level	Rnf166<em1(IMPC)J>/Rnf166<em1(IMPC)J>	C57BL/6NJ-Rnf166<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472206	F	MP:0010506	prolonged RR interval	Rnf166<em1(IMPC)J>/Rnf166<em1(IMPC)J>	C57BL/6NJ-Rnf166<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472206	M	MP:0001399	hyperactivity	Rnf166<em1(IMPC)J>/Rnf166<em1(IMPC)J>	C57BL/6NJ-Rnf166<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472207	F	MP:0005565	increased blood urea nitrogen level	Rnf187<em1(IMPC)J>/Rnf187<em1(IMPC)J>	C57BL/6NJ-Rnf187<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472208	F	MP:0005568	increased circulating total protein level	Romo1<em1(IMPC)Kmpc>/Romo1<+>	C57BL/6NTac-Romo1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472209	M	MP:0001700	abnormal embryo turning	Romo1<em1(IMPC)Kmpc>/Romo1<em1(IMPC)Kmpc>	C57BL/6NTac-Romo1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472210	F	MP:0000709	enlarged thymus	Ror1<em1(IMPC)Ccpcz>/Ror1<+>	C57BL/6NCrl-Ror1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472210	F	MP:0002989	small kidney	Ror1<em1(IMPC)Ccpcz>/Ror1<+>	C57BL/6NCrl-Ror1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472210	F	MP:0000703	abnormal thymus morphology	Ror1<em1(IMPC)Ccpcz>/Ror1<+>	C57BL/6NCrl-Ror1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472210	M	MP:0000691	enlarged spleen	Ror1<em1(IMPC)Ccpcz>/Ror1<+>	C57BL/6NCrl-Ror1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472210	F	MP:0001120	abnormal uterus morphology	Ror1<em1(IMPC)Ccpcz>/Ror1<+>	C57BL/6NCrl-Ror1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472210	M	MP:0000689	abnormal spleen morphology	Ror1<em1(IMPC)Ccpcz>/Ror1<+>	C57BL/6NCrl-Ror1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472210	F	MP:0009709	hydrometra	Ror1<em1(IMPC)Ccpcz>/Ror1<+>	C57BL/6NCrl-Ror1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472210	M	MP:0009141	increased prepulse inhibition	Ror1<em1(IMPC)Ccpcz>/Ror1<+>	C57BL/6NCrl-Ror1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472214	F	MP:0002092	abnormal eye morphology	S100a1<em1(IMPC)Mbp>/S100a1<em1(IMPC)Mbp>	C57BL/6NCrl-S100a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472214	F	MP:0001293	anophthalmia	S100a1<em1(IMPC)Mbp>/S100a1<em1(IMPC)Mbp>	C57BL/6NCrl-S100a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472214	M	MP:0001148	enlarged testis	S100a1<em1(IMPC)Mbp>/S100a1<em1(IMPC)Mbp>	C57BL/6NCrl-S100a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472214	M	MP:0001146	abnormal testis morphology	S100a1<em1(IMPC)Mbp>/S100a1<em1(IMPC)Mbp>	C57BL/6NCrl-S100a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472214	M	MP:0001147	small testis	S100a1<em1(IMPC)Mbp>/S100a1<em1(IMPC)Mbp>	C57BL/6NCrl-S100a1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472215	M	MP:0000689	abnormal spleen morphology	S100a3<em1(IMPC)Mbp>/S100a3<em1(IMPC)Mbp>	C57BL/6NCrl-S100a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472215	M	MP:0001304	cataract	S100a3<em1(IMPC)Mbp>/S100a3<em1(IMPC)Mbp>	C57BL/6NCrl-S100a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472215	M	MP:0002699	abnormal vitreous body morphology	S100a3<em1(IMPC)Mbp>/S100a3<em1(IMPC)Mbp>	C57BL/6NCrl-S100a3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472217	M	MP:0001147	small testis	Sall3<tm1.1(KOMP)Mbp>/Sall3<+>	C57BL/6NCrl-Sall3<tm1.1(KOMP)Mbp>/Ccpcz	N	MGI:5576271
MGI:7472217	F	MP:0000709	enlarged thymus	Sall3<tm1.1(KOMP)Mbp>/Sall3<+>	C57BL/6NCrl-Sall3<tm1.1(KOMP)Mbp>/Ccpcz	N	MGI:5576271
MGI:7472217	F	MP:0000703	abnormal thymus morphology	Sall3<tm1.1(KOMP)Mbp>/Sall3<+>	C57BL/6NCrl-Sall3<tm1.1(KOMP)Mbp>/Ccpcz	N	MGI:5576271
MGI:7472217	M	MP:0001146	abnormal testis morphology	Sall3<tm1.1(KOMP)Mbp>/Sall3<+>	C57BL/6NCrl-Sall3<tm1.1(KOMP)Mbp>/Ccpcz	N	MGI:5576271
MGI:7472217	M	MP:0000274	enlarged heart	Sall3<tm1.1(KOMP)Mbp>/Sall3<+>	C57BL/6NCrl-Sall3<tm1.1(KOMP)Mbp>/Ccpcz	N	MGI:5576271
MGI:7472217	F	MP:0005599	increased cardiac muscle contractility	Sall3<tm1.1(KOMP)Mbp>/Sall3<+>	C57BL/6NCrl-Sall3<tm1.1(KOMP)Mbp>/Ccpcz	N	MGI:5576271
MGI:7472217	M	MP:0001148	enlarged testis	Sall3<tm1.1(KOMP)Mbp>/Sall3<+>	C57BL/6NCrl-Sall3<tm1.1(KOMP)Mbp>/Ccpcz	N	MGI:5576271
MGI:7472217	M	MP:0001399	hyperactivity	Sall3<tm1.1(KOMP)Mbp>/Sall3<+>	C57BL/6NCrl-Sall3<tm1.1(KOMP)Mbp>/Ccpcz	N	MGI:5576271
MGI:7472217	F	MP:0002339	abnormal lymph node morphology	Sall3<tm1.1(KOMP)Mbp>/Sall3<+>	C57BL/6NCrl-Sall3<tm1.1(KOMP)Mbp>/Ccpcz	N	MGI:5576271
MGI:7472217	F	MP:0002060	abnormal skin morphology	Sall3<tm1.1(KOMP)Mbp>/Sall3<+>	C57BL/6NCrl-Sall3<tm1.1(KOMP)Mbp>/Ccpcz	N	MGI:5576271
MGI:7472217	F	MP:0001120	abnormal uterus morphology	Sall3<tm1.1(KOMP)Mbp>/Sall3<+>	C57BL/6NCrl-Sall3<tm1.1(KOMP)Mbp>/Ccpcz	N	MGI:5576271
MGI:7472217	M	MP:0000266	abnormal heart morphology	Sall3<tm1.1(KOMP)Mbp>/Sall3<+>	C57BL/6NCrl-Sall3<tm1.1(KOMP)Mbp>/Ccpcz	N	MGI:5576271
MGI:7472217	F	MP:0000702	enlarged lymph nodes	Sall3<tm1.1(KOMP)Mbp>/Sall3<+>	C57BL/6NCrl-Sall3<tm1.1(KOMP)Mbp>/Ccpcz	N	MGI:5576271
MGI:7472221	F	MP:0005553	increased circulating creatinine level	Scand1<em1(IMPC)H>/Scand1<em1(IMPC)H>	C57BL/6NTac-Scand1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472221	F	MP:0001399	hyperactivity	Scand1<em1(IMPC)H>/Scand1<em1(IMPC)H>	C57BL/6NTac-Scand1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472221	M	MP:0004953	decreased spleen weight	Scand1<em1(IMPC)H>/Scand1<em1(IMPC)H>	C57BL/6NTac-Scand1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472221	M	MP:0010068	decreased red blood cell distribution width	Scand1<em1(IMPC)H>/Scand1<em1(IMPC)H>	C57BL/6NTac-Scand1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472223	M	MP:0001146	abnormal testis morphology	Scel<em1(IMPC)Ccpcz>/Scel<em1(IMPC)Ccpcz>	C57BL/6NCrl-Scel<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472223	M	MP:0001147	small testis	Scel<em1(IMPC)Ccpcz>/Scel<em1(IMPC)Ccpcz>	C57BL/6NCrl-Scel<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472223	M	MP:0000274	enlarged heart	Scel<em1(IMPC)Ccpcz>/Scel<em1(IMPC)Ccpcz>	C57BL/6NCrl-Scel<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472223	M	MP:0000266	abnormal heart morphology	Scel<em1(IMPC)Ccpcz>/Scel<em1(IMPC)Ccpcz>	C57BL/6NCrl-Scel<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472223	F	MP:0000709	enlarged thymus	Scel<em1(IMPC)Ccpcz>/Scel<em1(IMPC)Ccpcz>	C57BL/6NCrl-Scel<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472223	F	MP:0002110	abnormal digit morphology	Scel<em1(IMPC)Ccpcz>/Scel<em1(IMPC)Ccpcz>	C57BL/6NCrl-Scel<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472223	F	MP:0000703	abnormal thymus morphology	Scel<em1(IMPC)Ccpcz>/Scel<em1(IMPC)Ccpcz>	C57BL/6NCrl-Scel<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472223	M	MP:0005633	increased circulating sodium level	Scel<em1(IMPC)Ccpcz>/Scel<em1(IMPC)Ccpcz>	C57BL/6NCrl-Scel<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472224	F	MP:0000691	enlarged spleen	Scg5<em1(IMPC)Mbp>/Scg5<em1(IMPC)Mbp>	C57BL/6NCrl-Scg5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472224	F	MP:0000689	abnormal spleen morphology	Scg5<em1(IMPC)Mbp>/Scg5<em1(IMPC)Mbp>	C57BL/6NCrl-Scg5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472224	M	MP:0001399	hyperactivity	Scg5<em1(IMPC)Mbp>/Scg5<em1(IMPC)Mbp>	C57BL/6NCrl-Scg5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472224	F	MP:0002968	increased circulating alkaline phosphatase level	Scg5<em1(IMPC)Mbp>/Scg5<em1(IMPC)Mbp>	C57BL/6NCrl-Scg5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472224	M	MP:0004924	abnormal behavior	Scg5<em1(IMPC)Mbp>/Scg5<em1(IMPC)Mbp>	C57BL/6NCrl-Scg5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472224	M	MP:0020870	decreased thigmotaxis	Scg5<em1(IMPC)Mbp>/Scg5<em1(IMPC)Mbp>	C57BL/6NCrl-Scg5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472224	F	MP:0002590	increased mean corpuscular volume	Scg5<em1(IMPC)Mbp>/Scg5<em1(IMPC)Mbp>	C57BL/6NCrl-Scg5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472224	M	MP:0001364	decreased anxiety-related response	Scg5<em1(IMPC)Mbp>/Scg5<em1(IMPC)Mbp>	C57BL/6NCrl-Scg5<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472226	F	MP:0001364	decreased anxiety-related response	Sgsm3<em1(IMPC)Bay>/Sgsm3<em1(IMPC)Bay>	C57BL/6N-Sgsm3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472226	F	MP:0001399	hyperactivity	Sgsm3<em1(IMPC)Bay>/Sgsm3<em1(IMPC)Bay>	C57BL/6N-Sgsm3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472227	M	MP:0020421	increased freezing behavior	Skic3<em1(IMPC)Tcp>/Skic3<+>	C57BL/6NCrl-Skic3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472227	M	MP:0011874	enlarged urinary bladder	Skic3<em1(IMPC)Tcp>/Skic3<+>	C57BL/6NCrl-Skic3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472227	M	MP:0005627	increased circulating potassium level	Skic3<em1(IMPC)Tcp>/Skic3<+>	C57BL/6NCrl-Skic3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472229	M	MP:0005635	decreased circulating bilirubin level	Skor1<em1(IMPC)J>/Skor1<+>	C57BL/6NJ-Skor1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472229	M	MP:0005559	increased circulating glucose level	Skor1<em1(IMPC)J>/Skor1<+>	C57BL/6NJ-Skor1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472231	F	MP:0003795	abnormal bone structure	Slc13a4<em1(IMPC)Hmgu>/Slc13a4<+>	C57BL/6NCrl-Slc13a4<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472232	F	MP:0010088	decreased circulating fructosamine level	Slc17a7<em1(IMPC)H>/Slc17a7<+>	C57BL/6N-Slc17a7<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472233	M	MP:0009141	increased prepulse inhibition	Slc24a3<em1(IMPC)Kmpc>/Slc24a3<em1(IMPC)Kmpc>	C57BL/6NTac-Slc24a3<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472233	M	MP:0010379	decreased respiratory quotient	Slc24a3<em1(IMPC)Kmpc>/Slc24a3<em1(IMPC)Kmpc>	C57BL/6NTac-Slc24a3<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472233	M	MP:0003179	thrombocytopenia	Slc24a3<em1(IMPC)Kmpc>/Slc24a3<em1(IMPC)Kmpc>	C57BL/6NTac-Slc24a3<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472233	M	MP:0002075	abnormal coat/hair pigmentation	Slc24a3<em1(IMPC)Kmpc>/Slc24a3<em1(IMPC)Kmpc>	C57BL/6NTac-Slc24a3<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472233	F	MP:0011941	increased fluid intake	Slc24a3<em1(IMPC)Kmpc>/Slc24a3<em1(IMPC)Kmpc>	C57BL/6NTac-Slc24a3<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472235	F	MP:0001697	abnormal embryo size	Slc25a1<em1(IMPC)Kmpc>/Slc25a1<em1(IMPC)Kmpc>	C57BL/6NTac-Slc25a1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472235	F	MP:0003984	embryonic growth retardation	Slc25a1<em1(IMPC)Kmpc>/Slc25a1<em1(IMPC)Kmpc>	C57BL/6NTac-Slc25a1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472236	M	MP:0000063	decreased bone mineral density	Slc25a39<em1(IMPC)Bay>/Slc25a39<+>	C57BL/6N-Slc25a39<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472240	F	MP:0000274	enlarged heart	Slc38a7<em1(IMPC)Ccpcz>/Slc38a7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Slc38a7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472240	F	MP:0000709	enlarged thymus	Slc38a7<em1(IMPC)Ccpcz>/Slc38a7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Slc38a7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472240	F	MP:0001293	anophthalmia	Slc38a7<em1(IMPC)Ccpcz>/Slc38a7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Slc38a7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472240	F	MP:0000703	abnormal thymus morphology	Slc38a7<em1(IMPC)Ccpcz>/Slc38a7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Slc38a7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472240	F	MP:0002092	abnormal eye morphology	Slc38a7<em1(IMPC)Ccpcz>/Slc38a7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Slc38a7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472240	F	MP:0000266	abnormal heart morphology	Slc38a7<em1(IMPC)Ccpcz>/Slc38a7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Slc38a7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472241	F	MP:0001399	hyperactivity	Slc38a8<em1(IMPC)Bay>/Slc38a8<em1(IMPC)Bay>	C57BL/6N-Slc38a8<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472243	F	MP:0001297	microphthalmia	Slc4a8<em1(IMPC)Mbp>/Slc4a8<em1(IMPC)Mbp>	C57BL/6NCrl-Slc4a8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472243	F	MP:0002092	abnormal eye morphology	Slc4a8<em1(IMPC)Mbp>/Slc4a8<em1(IMPC)Mbp>	C57BL/6NCrl-Slc4a8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472243	M	MP:0001488	increased startle reflex	Slc4a8<em1(IMPC)Mbp>/Slc4a8<em1(IMPC)Mbp>	C57BL/6NCrl-Slc4a8<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472244	F	MP:0005627	increased circulating potassium level	Slc7a5<em1(IMPC)H>/Slc7a5<+>	C57BL/6NTac-Slc7a5<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472244	F	MP:0002606	increased basophil cell number	Slc7a5<em1(IMPC)H>/Slc7a5<+>	C57BL/6NTac-Slc7a5<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472251	M	MP:0010392	prolonged QRS complex duration	Smim20<em1(IMPC)J>/Smim20<em1(IMPC)J>	C57BL/6NJ-Smim20<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472258	F	MP:0010090	increased circulating creatine kinase level	Stmn2<em1(IMPC)Kmpc>/Stmn2<+>	C57BL/6NTac-Stmn2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472258	M	MP:0010025	decreased total body fat amount	Stmn2<em1(IMPC)Kmpc>/Stmn2<+>	C57BL/6NTac-Stmn2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472258	M	MP:0001399	hyperactivity	Stmn2<em1(IMPC)Kmpc>/Stmn2<+>	C57BL/6NTac-Stmn2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472265	M	MP:0000266	abnormal heart morphology	Sult1a1<em1(IMPC)Ccpcz>/Sult1a1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Sult1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472265	F	MP:0005084	abnormal gallbladder morphology	Sult1a1<em1(IMPC)Ccpcz>/Sult1a1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Sult1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472265	M	MP:0000274	enlarged heart	Sult1a1<em1(IMPC)Ccpcz>/Sult1a1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Sult1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472265	M	MP:0001146	abnormal testis morphology	Sult1a1<em1(IMPC)Ccpcz>/Sult1a1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Sult1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472265	F	MP:0000709	enlarged thymus	Sult1a1<em1(IMPC)Ccpcz>/Sult1a1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Sult1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472265	M	MP:0000627	abnormal mammary gland morphology	Sult1a1<em1(IMPC)Ccpcz>/Sult1a1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Sult1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472265	F	MP:0002060	abnormal skin morphology	Sult1a1<em1(IMPC)Ccpcz>/Sult1a1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Sult1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472265	M	MP:0000759	abnormal skeletal muscle morphology	Sult1a1<em1(IMPC)Ccpcz>/Sult1a1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Sult1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472265	F	MP:0009342	enlarged gallbladder	Sult1a1<em1(IMPC)Ccpcz>/Sult1a1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Sult1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472265	F	MP:0000703	abnormal thymus morphology	Sult1a1<em1(IMPC)Ccpcz>/Sult1a1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Sult1a1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472267	F	MP:0002764	short tibia	Syngr1<em1(IMPC)Ccpcz>/Syngr1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Syngr1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472267	M	MP:0000759	abnormal skeletal muscle morphology	Syngr1<em1(IMPC)Ccpcz>/Syngr1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Syngr1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472267	F	MP:0001120	abnormal uterus morphology	Syngr1<em1(IMPC)Ccpcz>/Syngr1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Syngr1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472267	F	MP:0004906	enlarged uterus	Syngr1<em1(IMPC)Ccpcz>/Syngr1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Syngr1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472267	F	MP:0000703	abnormal thymus morphology	Syngr1<em1(IMPC)Ccpcz>/Syngr1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Syngr1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472267	F	MP:0000709	enlarged thymus	Syngr1<em1(IMPC)Ccpcz>/Syngr1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Syngr1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472268	M	MP:0002574	increased vertical activity	Syp<em1(IMPC)Bay>/Y	C57BL/6N-Syp<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472269	F	MP:0002574	increased vertical activity	Syp<em1(IMPC)Bay>/Syp<+>	C57BL/6N-Syp<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472270	F	MP:0002092	abnormal eye morphology	Taf15<em1(IMPC)Mbp>/Taf15<em1(IMPC)Mbp>	C57BL/6NCrl-Taf15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472270	F	MP:0005013	increased lymphocyte cell number	Taf15<em1(IMPC)Mbp>/Taf15<em1(IMPC)Mbp>	C57BL/6NCrl-Taf15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472270	M	MP:0013279	increased fasting circulating glucose level	Taf15<em1(IMPC)Mbp>/Taf15<em1(IMPC)Mbp>	C57BL/6NCrl-Taf15<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472274	F	MP:0002339	abnormal lymph node morphology	Tcaf2<em1(IMPC)Ccpcz>/Tcaf2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tcaf2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472274	F	MP:0000759	abnormal skeletal muscle morphology	Tcaf2<em1(IMPC)Ccpcz>/Tcaf2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tcaf2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472274	F	MP:0001293	anophthalmia	Tcaf2<em1(IMPC)Ccpcz>/Tcaf2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tcaf2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472274	F	MP:0000703	abnormal thymus morphology	Tcaf2<em1(IMPC)Ccpcz>/Tcaf2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tcaf2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472274	F	MP:0002092	abnormal eye morphology	Tcaf2<em1(IMPC)Ccpcz>/Tcaf2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tcaf2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472274	F	MP:0000689	abnormal spleen morphology	Tcaf2<em1(IMPC)Ccpcz>/Tcaf2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tcaf2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472274	F	MP:0000702	enlarged lymph nodes	Tcaf2<em1(IMPC)Ccpcz>/Tcaf2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tcaf2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472274	M	MP:0005564	increased hemoglobin content	Tcaf2<em1(IMPC)Ccpcz>/Tcaf2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tcaf2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472274	F	MP:0000691	enlarged spleen	Tcaf2<em1(IMPC)Ccpcz>/Tcaf2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tcaf2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472274	F	MP:0000709	enlarged thymus	Tcaf2<em1(IMPC)Ccpcz>/Tcaf2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tcaf2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472275	M	MP:0000194	increased circulating calcium level	Tcf21<em1(IMPC)Mbp>/Tcf21<+>	C57BL/6NCrl-Tcf21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472275	F	MP:0001126	abnormal ovary morphology	Tcf21<em1(IMPC)Mbp>/Tcf21<+>	C57BL/6NCrl-Tcf21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472275	M	MP:0002135	abnormal kidney morphology	Tcf21<em1(IMPC)Mbp>/Tcf21<+>	C57BL/6NCrl-Tcf21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472275	M	MP:0000692	small spleen	Tcf21<em1(IMPC)Mbp>/Tcf21<+>	C57BL/6NCrl-Tcf21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472275	M	MP:0003068	enlarged kidney	Tcf21<em1(IMPC)Mbp>/Tcf21<+>	C57BL/6NCrl-Tcf21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472275	F	MP:0001293	anophthalmia	Tcf21<em1(IMPC)Mbp>/Tcf21<+>	C57BL/6NCrl-Tcf21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472275	M	MP:0001148	enlarged testis	Tcf21<em1(IMPC)Mbp>/Tcf21<+>	C57BL/6NCrl-Tcf21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472275	M	MP:0001146	abnormal testis morphology	Tcf21<em1(IMPC)Mbp>/Tcf21<+>	C57BL/6NCrl-Tcf21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472275	M	MP:0000689	abnormal spleen morphology	Tcf21<em1(IMPC)Mbp>/Tcf21<+>	C57BL/6NCrl-Tcf21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472275	F	MP:0002092	abnormal eye morphology	Tcf21<em1(IMPC)Mbp>/Tcf21<+>	C57BL/6NCrl-Tcf21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472276	F	MP:0003231	abnormal placenta vasculature	Tcf21<em1(IMPC)Mbp>/Tcf21<em1(IMPC)Mbp>	C57BL/6NCrl-Tcf21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472276	F	MP:0001297	microphthalmia	Tcf21<em1(IMPC)Mbp>/Tcf21<em1(IMPC)Mbp>	C57BL/6NCrl-Tcf21<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472277	M	MP:0002217	small lymph nodes	Tekt1<em1(IMPC)Ccpcz>/Tekt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tekt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472277	M	MP:0000274	enlarged heart	Tekt1<em1(IMPC)Ccpcz>/Tekt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tekt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472277	M	MP:0000266	abnormal heart morphology	Tekt1<em1(IMPC)Ccpcz>/Tekt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tekt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472277	F	MP:0000709	enlarged thymus	Tekt1<em1(IMPC)Ccpcz>/Tekt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tekt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472277	M	MP:0002339	abnormal lymph node morphology	Tekt1<em1(IMPC)Ccpcz>/Tekt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tekt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472277	F	MP:0000703	abnormal thymus morphology	Tekt1<em1(IMPC)Ccpcz>/Tekt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tekt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472277	M	MP:0010024	increased total body fat amount	Tekt1<em1(IMPC)Ccpcz>/Tekt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tekt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472279	F	MP:0001399	hyperactivity	Tfpi2<em1(IMPC)Kmpc>/Tfpi2<em1(IMPC)Kmpc>	C57BL/6NTac-Tfpi2<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472281	F	MP:0000691	enlarged spleen	Tincr<em1(IMPC)Ccpcz>/Tincr<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tincr<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472281	F	MP:0005599	increased cardiac muscle contractility	Tincr<em1(IMPC)Ccpcz>/Tincr<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tincr<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472281	F	MP:0000689	abnormal spleen morphology	Tincr<em1(IMPC)Ccpcz>/Tincr<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tincr<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472281	F	MP:0000702	enlarged lymph nodes	Tincr<em1(IMPC)Ccpcz>/Tincr<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tincr<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472281	F	MP:0002339	abnormal lymph node morphology	Tincr<em1(IMPC)Ccpcz>/Tincr<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tincr<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472282	M	MP:0000266	abnormal heart morphology	Tkfc<em1(IMPC)Ccpcz>/Tkfc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tkfc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472282	M	MP:0000703	abnormal thymus morphology	Tkfc<em1(IMPC)Ccpcz>/Tkfc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tkfc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472282	F	MP:0001333	absent optic nerve	Tkfc<em1(IMPC)Ccpcz>/Tkfc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tkfc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472282	M	MP:0000274	enlarged heart	Tkfc<em1(IMPC)Ccpcz>/Tkfc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tkfc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472282	F	MP:0001330	abnormal optic nerve morphology	Tkfc<em1(IMPC)Ccpcz>/Tkfc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tkfc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472282	M	MP:0000709	enlarged thymus	Tkfc<em1(IMPC)Ccpcz>/Tkfc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tkfc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472283	M	MP:0010052	increased grip strength	Tm4sf5<em1(IMPC)Kmpc>/Tm4sf5<em1(IMPC)Kmpc>	C57BL/6NTac-Tm4sf5<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472283	F	MP:0011942	decreased fluid intake	Tm4sf5<em1(IMPC)Kmpc>/Tm4sf5<em1(IMPC)Kmpc>	C57BL/6NTac-Tm4sf5<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472285	M	MP:0009455	enhanced cued conditioning behavior	Tmem132e<em1(IMPC)Kmpc>/Tmem132e<+>	C57BL/6NTac-Tmem132e<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472288	M	MP:0001402	decreased locomotor activity	Tmsb4x<em1(IMPC)Mbp>/Y	C57BL/6NCrl-Tmsb4x<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472289	F	MP:0000691	enlarged spleen	Tmsb4x<em1(IMPC)Mbp>/Tmsb4x<em1(IMPC)Mbp>	C57BL/6NCrl-Tmsb4x<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472289	F	MP:0000689	abnormal spleen morphology	Tmsb4x<em1(IMPC)Mbp>/Tmsb4x<em1(IMPC)Mbp>	C57BL/6NCrl-Tmsb4x<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472289	F	MP:0020870	decreased thigmotaxis	Tmsb4x<em1(IMPC)Mbp>/Tmsb4x<em1(IMPC)Mbp>	C57BL/6NCrl-Tmsb4x<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472289	F	MP:0001364	decreased anxiety-related response	Tmsb4x<em1(IMPC)Mbp>/Tmsb4x<em1(IMPC)Mbp>	C57BL/6NCrl-Tmsb4x<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472289	F	MP:0004924	abnormal behavior	Tmsb4x<em1(IMPC)Mbp>/Tmsb4x<em1(IMPC)Mbp>	C57BL/6NCrl-Tmsb4x<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472289	F	MP:0002060	abnormal skin morphology	Tmsb4x<em1(IMPC)Mbp>/Tmsb4x<em1(IMPC)Mbp>	C57BL/6NCrl-Tmsb4x<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472289	F	MP:0001402	decreased locomotor activity	Tmsb4x<em1(IMPC)Mbp>/Tmsb4x<em1(IMPC)Mbp>	C57BL/6NCrl-Tmsb4x<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472290	M	MP:0009453	enhanced contextual conditioning behavior	Tmtc2<em2(IMPC)Kmpc>/Tmtc2<em2(IMPC)Kmpc>	C57BL/6NTac-Tmtc2<em2(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472291	M	MP:0000219	increased neutrophil cell number	Tnfrsf1a<em1(IMPC)Ccpcz>/Tnfrsf1a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tnfrsf1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472291	M	MP:0005343	increased circulating aspartate transaminase level	Tnfrsf1a<em1(IMPC)Ccpcz>/Tnfrsf1a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tnfrsf1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472291	M	MP:0000266	abnormal heart morphology	Tnfrsf1a<em1(IMPC)Ccpcz>/Tnfrsf1a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tnfrsf1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472291	F	MP:0002060	abnormal skin morphology	Tnfrsf1a<em1(IMPC)Ccpcz>/Tnfrsf1a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tnfrsf1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472291	M	MP:0000274	enlarged heart	Tnfrsf1a<em1(IMPC)Ccpcz>/Tnfrsf1a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tnfrsf1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472291	M	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number	Tnfrsf1a<em1(IMPC)Ccpcz>/Tnfrsf1a<em1(IMPC)Ccpcz>	C57BL/6NCrl-Tnfrsf1a<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472292	F	MP:0000601	small liver	Tnn<em1(IMPC)Mbp>/Tnn<em1(IMPC)Mbp>	C57BL/6NCrl-Tnn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472292	F	MP:0000689	abnormal spleen morphology	Tnn<em1(IMPC)Mbp>/Tnn<em1(IMPC)Mbp>	C57BL/6NCrl-Tnn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472292	F	MP:0000598	abnormal liver morphology	Tnn<em1(IMPC)Mbp>/Tnn<em1(IMPC)Mbp>	C57BL/6NCrl-Tnn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472292	F	MP:0000691	enlarged spleen	Tnn<em1(IMPC)Mbp>/Tnn<em1(IMPC)Mbp>	C57BL/6NCrl-Tnn<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7472294	M	MP:0002100	abnormal tooth morphology	Tppp3<em1(IMPC)Ccpcz>/Tppp3<+>	C57BL/6NCrl-Tppp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472294	F	MP:0008039	increased NK T cell number	Tppp3<em1(IMPC)Ccpcz>/Tppp3<+>	C57BL/6NCrl-Tppp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472294	F	MP:0013523	increased memory-marker CD4-positive NK T cell number	Tppp3<em1(IMPC)Ccpcz>/Tppp3<+>	C57BL/6NCrl-Tppp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472294	F	MP:0000691	enlarged spleen	Tppp3<em1(IMPC)Ccpcz>/Tppp3<+>	C57BL/6NCrl-Tppp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472294	F	MP:0002339	abnormal lymph node morphology	Tppp3<em1(IMPC)Ccpcz>/Tppp3<+>	C57BL/6NCrl-Tppp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472294	M	MP:0013129	abnormal tooth color	Tppp3<em1(IMPC)Ccpcz>/Tppp3<+>	C57BL/6NCrl-Tppp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472294	F	MP:0000689	abnormal spleen morphology	Tppp3<em1(IMPC)Ccpcz>/Tppp3<+>	C57BL/6NCrl-Tppp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472294	F	MP:0000702	enlarged lymph nodes	Tppp3<em1(IMPC)Ccpcz>/Tppp3<+>	C57BL/6NCrl-Tppp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472294	F	MP:0013520	increased CD4-positive NK T cell number	Tppp3<em1(IMPC)Ccpcz>/Tppp3<+>	C57BL/6NCrl-Tppp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472296	F	MP:0000160	kyphosis	Tpte<em1(IMPC)Kmpc>/Tpte<em1(IMPC)Kmpc>	C57BL/6NTac-Tpte<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472296	F	MP:0004174	abnormal spine curvature	Tpte<em1(IMPC)Kmpc>/Tpte<em1(IMPC)Kmpc>	C57BL/6NTac-Tpte<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472299	F	MP:0000063	decreased bone mineral density	Tspan13<em1(IMPC)Kmpc>/Tspan13<em1(IMPC)Kmpc>	C57BL/6NTac-Tspan13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472299	F	MP:0002098	abnormal vibrissa morphology	Tspan13<em1(IMPC)Kmpc>/Tspan13<em1(IMPC)Kmpc>	C57BL/6NTac-Tspan13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472299	F	MP:0004924	abnormal behavior	Tspan13<em1(IMPC)Kmpc>/Tspan13<em1(IMPC)Kmpc>	C57BL/6NTac-Tspan13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472299	M	MP:0013278	decreased fasting circulating glucose level	Tspan13<em1(IMPC)Kmpc>/Tspan13<em1(IMPC)Kmpc>	C57BL/6NTac-Tspan13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472299	F	MP:0010124	decreased bone mineral content	Tspan13<em1(IMPC)Kmpc>/Tspan13<em1(IMPC)Kmpc>	C57BL/6NTac-Tspan13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472299	M	MP:0002833	increased heart weight	Tspan13<em1(IMPC)Kmpc>/Tspan13<em1(IMPC)Kmpc>	C57BL/6NTac-Tspan13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472299	F	MP:0003795	abnormal bone structure	Tspan13<em1(IMPC)Kmpc>/Tspan13<em1(IMPC)Kmpc>	C57BL/6NTac-Tspan13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472299	F	MP:0020870	decreased thigmotaxis	Tspan13<em1(IMPC)Kmpc>/Tspan13<em1(IMPC)Kmpc>	C57BL/6NTac-Tspan13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472299	M	MP:0010052	increased grip strength	Tspan13<em1(IMPC)Kmpc>/Tspan13<em1(IMPC)Kmpc>	C57BL/6NTac-Tspan13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472299	M	MP:0009142	decreased prepulse inhibition	Tspan13<em1(IMPC)Kmpc>/Tspan13<em1(IMPC)Kmpc>	C57BL/6NTac-Tspan13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472299	F	MP:0010024	increased total body fat amount	Tspan13<em1(IMPC)Kmpc>/Tspan13<em1(IMPC)Kmpc>	C57BL/6NTac-Tspan13<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7472300	M	MP:0002098	abnormal vibrissa morphology	Tspan15<em1(IMPC)Hmgu>/Tspan15<+>	C57BL/6NCrl-Tspan15<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472300	M	MP:0002059	abnormal seminal vesicle morphology	Tspan15<em1(IMPC)Hmgu>/Tspan15<+>	C57BL/6NCrl-Tspan15<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472302	M	MP:0000745	tremors	Ttbk1<em1(IMPC)J>/Ttbk1<em1(IMPC)J>	C57BL/6NJ-Ttbk1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472302	M	MP:0010025	decreased total body fat amount	Ttbk1<em1(IMPC)J>/Ttbk1<em1(IMPC)J>	C57BL/6NJ-Ttbk1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472302	M	MP:0013279	increased fasting circulating glucose level	Ttbk1<em1(IMPC)J>/Ttbk1<em1(IMPC)J>	C57BL/6NJ-Ttbk1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472302	F	MP:0001488	increased startle reflex	Ttbk1<em1(IMPC)J>/Ttbk1<em1(IMPC)J>	C57BL/6NJ-Ttbk1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472302	F	MP:0001417	decreased exploration in new environment	Ttbk1<em1(IMPC)J>/Ttbk1<em1(IMPC)J>	C57BL/6NJ-Ttbk1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472302	M	MP:0010052	increased grip strength	Ttbk1<em1(IMPC)J>/Ttbk1<em1(IMPC)J>	C57BL/6NJ-Ttbk1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472302	M	MP:0003960	increased lean body mass	Ttbk1<em1(IMPC)J>/Ttbk1<em1(IMPC)J>	C57BL/6NJ-Ttbk1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472302	M	MP:0005559	increased circulating glucose level	Ttbk1<em1(IMPC)J>/Ttbk1<em1(IMPC)J>	C57BL/6NJ-Ttbk1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472304	M	MP:0005178	increased circulating cholesterol level	Ttc17<em1(IMPC)J>/Ttc17<em1(IMPC)J>	C57BL/6NJ-Ttc17<em1(IMPC)J>/J	N	MGI:5576271
MGI:7472304	F	MP:0001488	increased startle reflex	Ttc17<em1(IMPC)J>/Ttc17<em1(IMPC)J>	C57BL/6NJ-Ttc17<em1(IMPC)J>/J	N	MGI:5576271
MGI:7472308	M	MP:0001402	decreased locomotor activity	Tubg1<tm1dIcs>/Tubg1<+>	C57BL/6N-Tubg1<tm1dIcs>/Ics	N	MGI:5576271
MGI:7472310	M	MP:0010507	shortened RR interval	Ubr7<em1(IMPC)Tcp>/Ubr7<em1(IMPC)Tcp>	C57BL/6NCrl-Ubr7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472310	F	MP:0005013	increased lymphocyte cell number	Ubr7<em1(IMPC)Tcp>/Ubr7<em1(IMPC)Tcp>	C57BL/6NCrl-Ubr7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472310	F	MP:0000218	increased leukocyte cell number	Ubr7<em1(IMPC)Tcp>/Ubr7<em1(IMPC)Tcp>	C57BL/6NCrl-Ubr7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472310	F	MP:0002792	abnormal retina vasculature morphology	Ubr7<em1(IMPC)Tcp>/Ubr7<em1(IMPC)Tcp>	C57BL/6NCrl-Ubr7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472310	M	MP:0002626	increased heart rate	Ubr7<em1(IMPC)Tcp>/Ubr7<em1(IMPC)Tcp>	C57BL/6NCrl-Ubr7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472310	M	MP:0005419	decreased circulating serum albumin level	Ubr7<em1(IMPC)Tcp>/Ubr7<em1(IMPC)Tcp>	C57BL/6NCrl-Ubr7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472310	M	MP:0001325	abnormal retina morphology	Ubr7<em1(IMPC)Tcp>/Ubr7<em1(IMPC)Tcp>	C57BL/6NCrl-Ubr7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472310	M	MP:0001488	increased startle reflex	Ubr7<em1(IMPC)Tcp>/Ubr7<em1(IMPC)Tcp>	C57BL/6NCrl-Ubr7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472310	M	MP:0005562	decreased mean corpuscular hemoglobin	Ubr7<em1(IMPC)Tcp>/Ubr7<em1(IMPC)Tcp>	C57BL/6NCrl-Ubr7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472310	F	MP:0010097	abnormal retina blood vessel morphology	Ubr7<em1(IMPC)Tcp>/Ubr7<em1(IMPC)Tcp>	C57BL/6NCrl-Ubr7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472310	M	MP:0005292	improved glucose tolerance	Ubr7<em1(IMPC)Tcp>/Ubr7<em1(IMPC)Tcp>	C57BL/6NCrl-Ubr7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7472314	F	MP:0005278	abnormal cholesterol homeostasis	Unc119b<tm1.1(KOMP)Vlcg>/Unc119b<tm1.1(KOMP)Vlcg>	C57BL/6N-Unc119b<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7472315	F	MP:0003450	enlarged pancreas	Uox<em1(IMPC)Ccpcz>/Uox<+>	C57BL/6NCrl-Uox<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472315	M	MP:0004247	small pancreas	Uox<em1(IMPC)Ccpcz>/Uox<+>	C57BL/6NCrl-Uox<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472318	M	MP:0005642	decreased mean corpuscular hemoglobin concentration	Usp32<em1(IMPC)Mhzh>/Usp32<+>	C57BL/6N-Usp32<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472318	M	MP:0005013	increased lymphocyte cell number	Usp32<em1(IMPC)Mhzh>/Usp32<+>	C57BL/6N-Usp32<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472318	M	MP:0000218	increased leukocyte cell number	Usp32<em1(IMPC)Mhzh>/Usp32<+>	C57BL/6N-Usp32<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472318	M	MP:0005419	decreased circulating serum albumin level	Usp32<em1(IMPC)Mhzh>/Usp32<+>	C57BL/6N-Usp32<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472318	M	MP:0005505	thrombocytosis	Usp32<em1(IMPC)Mhzh>/Usp32<+>	C57BL/6N-Usp32<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472318	M	MP:0002599	increased mean platelet volume	Usp32<em1(IMPC)Mhzh>/Usp32<+>	C57BL/6N-Usp32<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472318	M	MP:0010067	increased red blood cell distribution width	Usp32<em1(IMPC)Mhzh>/Usp32<+>	C57BL/6N-Usp32<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472318	M	MP:0002590	increased mean corpuscular volume	Usp32<em1(IMPC)Mhzh>/Usp32<+>	C57BL/6N-Usp32<em1(IMPC)Mhzh>/Mhzh	N	MGI:5576271
MGI:7472320	M	MP:0000274	enlarged heart	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	F	MP:0001417	decreased exploration in new environment	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	M	MP:0002997	enlarged seminal vesicle	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	F	MP:0003271	abnormal duodenum morphology	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	M	MP:0000266	abnormal heart morphology	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	F	MP:0001175	abnormal lung morphology	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	F	MP:0002339	abnormal lymph node morphology	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	F	MP:0004882	enlarged lung	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	F	MP:0003068	enlarged kidney	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	M	MP:0002059	abnormal seminal vesicle morphology	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	F	MP:0000691	enlarged spleen	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	F	MP:0000689	abnormal spleen morphology	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	F	MP:0002135	abnormal kidney morphology	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	F	MP:0000702	enlarged lymph nodes	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472320	M	MP:0000759	abnormal skeletal muscle morphology	Vamp4<em1(IMPC)Ccpcz>/Vamp4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vamp4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	F	MP:0000274	enlarged heart	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	F	MP:0000689	abnormal spleen morphology	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	F	MP:0000709	enlarged thymus	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	F	MP:0001120	abnormal uterus morphology	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	F	MP:0002135	abnormal kidney morphology	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	M	MP:0001157	small seminal vesicle	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	M	MP:0002059	abnormal seminal vesicle morphology	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	F	MP:0004906	enlarged uterus	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	F	MP:0000691	enlarged spleen	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	F	MP:0004122	abnormal sinus arrhythmia	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	F	MP:0000703	abnormal thymus morphology	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	F	MP:0002060	abnormal skin morphology	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	F	MP:0000266	abnormal heart morphology	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472321	F	MP:0010025	decreased total body fat amount	Vnn3<em1(IMPC)Ccpcz>/Vnn3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vnn3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7472323	M	MP:0020870	decreased thigmotaxis	Wdr64<em1(IMPC)Bay>/Wdr64<+>	C57BL/6N-Wdr64<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7472326	F	MP:0002968	increased circulating alkaline phosphatase level	Yif1a<em1(IMPC)J>/Yif1a<em1(IMPC)J>	C57BL/6NJ-Yif1a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472327	M	MP:0005562	decreased mean corpuscular hemoglobin	Zcchc2<em1(IMPC)J>/Zcchc2<em1(IMPC)J>	C57BL/6NJ-Zcchc2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472328	F	MP:0005344	increased circulating bilirubin level	Zcchc3<em1(IMPC)J>/Zcchc3<em1(IMPC)J>	C57BL/6NJ-Zcchc3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472328	F	MP:0002965	increased circulating serum albumin level	Zcchc3<em1(IMPC)J>/Zcchc3<em1(IMPC)J>	C57BL/6NJ-Zcchc3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472329	M	MP:0000221	decreased leukocyte cell number	Zdbf2<em1(IMPC)J>/Zdbf2<em1(IMPC)J>	C57BL/6NJ-Zdbf2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472330	F	MP:0000062	increased bone mineral density	Zdhhc16<tm1b(EUCOMM)Hmgu>/Zdhhc16<+>	C57BL/6NTac-Zdhhc16<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:7472330	F	MP:0003961	decreased lean body mass	Zdhhc16<tm1b(EUCOMM)Hmgu>/Zdhhc16<+>	C57BL/6NTac-Zdhhc16<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:7472330	M	MP:0001529	abnormal vocalization	Zdhhc16<tm1b(EUCOMM)Hmgu>/Zdhhc16<+>	C57BL/6NTac-Zdhhc16<tm1b(EUCOMM)Hmgu>/H	N	MGI:5576271
MGI:7472332	M	MP:0010052	increased grip strength	Zfp146<em1(IMPC)J>/Zfp146<em1(IMPC)J>	C57BL/6NJ-Zfp146<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472333	F	MP:0002968	increased circulating alkaline phosphatase level	Zfp513<em1(IMPC)J>/Zfp513<em1(IMPC)J>	C57BL/6NJ-Zfp513<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472333	F	MP:0005559	increased circulating glucose level	Zfp513<em1(IMPC)J>/Zfp513<em1(IMPC)J>	C57BL/6NJ-Zfp513<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472333	F	MP:0005635	decreased circulating bilirubin level	Zfp513<em1(IMPC)J>/Zfp513<em1(IMPC)J>	C57BL/6NJ-Zfp513<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7472334	M	MP:0001556	increased circulating HDL cholesterol level	Zfp532<em1(IMPC)J>/Zfp532<+>	C57BL/6NJ-Zfp532<em1(IMPC)J>/J	N	MGI:5576271
MGI:7472334	M	MP:0003131	increased erythrocyte cell number	Zfp532<em1(IMPC)J>/Zfp532<+>	C57BL/6NJ-Zfp532<em1(IMPC)J>/J	N	MGI:5576271
MGI:7472334	M	MP:0002591	decreased mean corpuscular volume	Zfp532<em1(IMPC)J>/Zfp532<+>	C57BL/6NJ-Zfp532<em1(IMPC)J>/J	N	MGI:5576271
MGI:7472336	F	MP:0005012	decreased eosinophil cell number	Zftraf1<em1(IMPC)H>/Zftraf1<em1(IMPC)H>	C57BL/6NTac-Zftraf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472336	M	MP:0010068	decreased red blood cell distribution width	Zftraf1<em1(IMPC)H>/Zftraf1<em1(IMPC)H>	C57BL/6NTac-Zftraf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472336	F	MP:0010052	increased grip strength	Zftraf1<em1(IMPC)H>/Zftraf1<em1(IMPC)H>	C57BL/6NTac-Zftraf1<em1(IMPC)H>/H	N	MGI:5576271
MGI:7472337	M	MP:0005343	increased circulating aspartate transaminase level	Zmat5<em1(IMPC)Hmgu>/Zmat5<+>	C57BL/6NCrl-Zmat5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7472337	M	MP:0010052	increased grip strength	Zmat5<em1(IMPC)Hmgu>/Zmat5<+>	C57BL/6NCrl-Zmat5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7482547	F	MP:0010308	decreased tumor latency	Atrx<tm1Rjg>/Atrx<tm1Rjg>,Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0	involves: 129P2/OlaHsd * 129S4/SvJae * CD-1	N	36073547
MGI:7482547	F	MP:0003789	increased osteosarcoma incidence	Atrx<tm1Rjg>/Atrx<tm1Rjg>,Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0	involves: 129P2/OlaHsd * 129S4/SvJae * CD-1	N	36073547
MGI:7482548	M	MP:0010308	decreased tumor latency	Atrx<tm1Rjg>/Y,Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0	involves: 129P2/OlaHsd * 129S4/SvJae * CD-1	N	36073547
MGI:7482548	M	MP:0003789	increased osteosarcoma incidence	Atrx<tm1Rjg>/Y,Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0	involves: 129P2/OlaHsd * 129S4/SvJae * CD-1	N	36073547
MGI:7482599	M	MP:0001544	abnormal cardiovascular system physiology	Actn2<em1Kage>/Actn2<+>	C57BL/6-Actn2<em1Kage>	N	36899856
MGI:7484362	F	MP:0002404	increased intestinal adenoma incidence	Tg(TetOp-Polb/tTA)2Sbl/0	B6.Cg-Tg(TetOp-Polb/tTA)2Sbl	N	19654874
MGI:7484362	M	MP:0010313	increased osteoma incidence	Tg(TetOp-Polb/tTA)2Sbl/0	B6.Cg-Tg(TetOp-Polb/tTA)2Sbl	N	19654874
MGI:7484362	F	MP:0002111	abnormal tail morphology	Tg(TetOp-Polb/tTA)2Sbl/0	B6.Cg-Tg(TetOp-Polb/tTA)2Sbl	N	19654874
MGI:7485800	F	MP:0011101	prenatal lethality, incomplete penetrance	Pml<tm1Ppp>/Pml<+>,Trp53<tm3.1Glo>/Trp53<tm3.1Glo>	B6.129S7(Cg)-Pml<tm1Ppp> Trp53<tm3.1Glo>	N	23656786
MGI:7485800	M	MP:0002083	premature death	Pml<tm1Ppp>/Pml<+>,Trp53<tm3.1Glo>/Trp53<tm3.1Glo>	B6.129S7(Cg)-Pml<tm1Ppp> Trp53<tm3.1Glo>	N	23656786
MGI:7485803	F	MP:0011101	prenatal lethality, incomplete penetrance	Pml<tm1Ppp>/Pml<tm1Ppp>,Trp53<tm3.1Glo>/Trp53<tm3.1Glo>	B6.129S7(Cg)-Pml<tm1Ppp> Trp53<tm3.1Glo>	N	23656786
MGI:7485803	M	MP:0002083	premature death	Pml<tm1Ppp>/Pml<tm1Ppp>,Trp53<tm3.1Glo>/Trp53<tm3.1Glo>	B6.129S7(Cg)-Pml<tm1Ppp> Trp53<tm3.1Glo>	N	23656786
MGI:7485831	F	MP:0002038	increased carcinoma incidence	Pml<tm1Ppp>/Pml<+>,Trp53<tm3.1Glo>/Trp53<+>	B6.129S7(Cg)-Pml<tm1Ppp> Trp53<tm3.1Glo>	N	23656786
MGI:7485831	M	MP:0014237	decreased tumor-free survival time	Pml<tm1Ppp>/Pml<+>,Trp53<tm3.1Glo>/Trp53<+>	B6.129S7(Cg)-Pml<tm1Ppp> Trp53<tm3.1Glo>	N	23656786
MGI:7485838	F	MP:0002038	increased carcinoma incidence	Pml<tm1Ppp>/Pml<tm1Ppp>,Trp53<tm3.1Glo>/Trp53<+>	B6.129S7(Cg)-Pml<tm1Ppp> Trp53<tm3.1Glo>	N	23656786
MGI:7485838	M	MP:0014237	decreased tumor-free survival time	Pml<tm1Ppp>/Pml<tm1Ppp>,Trp53<tm3.1Glo>/Trp53<+>	B6.129S7(Cg)-Pml<tm1Ppp> Trp53<tm3.1Glo>	N	23656786
MGI:7488007	M	MP:0009839	multiflagellated sperm	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0031373	abnormal manchette perinuclear ring morphology	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0002687	oligozoospermia	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0009239	short sperm flagellum	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0005578	teratozoospermia	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0002660	abnormal caput epididymis morphology	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0031354	abnormal acrosome assembly	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0008545	absent sperm flagellum	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0009238	coiled sperm flagellum	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0009838	abnormal sperm axoneme morphology	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0031386	elongated manchette	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0009230	abnormal sperm head morphology	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0001156	abnormal spermatogenesis	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0031374	abnormal manchette assembly	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0001925	male infertility	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0008892	abnormal sperm flagellum morphology	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0005389	reproductive system phenotype	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	Y	36756949
MGI:7488007	M	MP:0020451	decreased sperm progressive motility	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0031356	abnormal outer dense fiber morphology	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0001932	abnormal spermiogenesis	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0009830	abnormal sperm connecting piece morphology	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488007	M	MP:0002675	asthenozoospermia	Cep78<em1Xjg>/Cep78<em1Xjg>	C57BL/6J-Cep78<em1Xjg>	N	36756949
MGI:7488034	M	MP:0001925	male infertility	Tssk3<em1Amsa>/Tssk3<em1Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488034	M	MP:0009231	detached acrosome	Tssk3<em1Amsa>/Tssk3<em1Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488034	M	MP:0009838	abnormal sperm axoneme morphology	Tssk3<em1Amsa>/Tssk3<em1Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488034	M	MP:0008892	abnormal sperm flagellum morphology	Tssk3<em1Amsa>/Tssk3<em1Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488034	M	MP:0002687	oligozoospermia	Tssk3<em1Amsa>/Tssk3<em1Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488034	M	MP:0009230	abnormal sperm head morphology	Tssk3<em1Amsa>/Tssk3<em1Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488034	M	MP:0001932	abnormal spermiogenesis	Tssk3<em1Amsa>/Tssk3<em1Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488034	M	MP:0031356	abnormal outer dense fiber morphology	Tssk3<em1Amsa>/Tssk3<em1Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488034	M	MP:0005578	teratozoospermia	Tssk3<em1Amsa>/Tssk3<em1Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488034	M	MP:0020869	immotile sperm	Tssk3<em1Amsa>/Tssk3<em1Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488034	M	MP:0001155	arrest of spermatogenesis	Tssk3<em1Amsa>/Tssk3<em1Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488035	M	MP:0001932	abnormal spermiogenesis	Tssk3<em2Amsa>/Tssk3<em2Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488035	M	MP:0001155	arrest of spermatogenesis	Tssk3<em2Amsa>/Tssk3<em2Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488035	M	MP:0001925	male infertility	Tssk3<em2Amsa>/Tssk3<em2Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488035	M	MP:0002687	oligozoospermia	Tssk3<em2Amsa>/Tssk3<em2Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488035	M	MP:0020869	immotile sperm	Tssk3<em2Amsa>/Tssk3<em2Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488035	M	MP:0005578	teratozoospermia	Tssk3<em2Amsa>/Tssk3<em2Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488037	M	MP:0001932	abnormal spermiogenesis	Tssk3<em3Amsa>/Tssk3<em3Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488037	M	MP:0020869	immotile sperm	Tssk3<em3Amsa>/Tssk3<em3Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488037	M	MP:0001925	male infertility	Tssk3<em3Amsa>/Tssk3<em3Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488037	M	MP:0005578	teratozoospermia	Tssk3<em3Amsa>/Tssk3<em3Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488037	M	MP:0001155	arrest of spermatogenesis	Tssk3<em3Amsa>/Tssk3<em3Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488037	M	MP:0002687	oligozoospermia	Tssk3<em3Amsa>/Tssk3<em3Amsa>	involves: C57BL/6J * DBA/2J	N	34623009
MGI:7488110	M	MP:0009830	abnormal sperm connecting piece morphology	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0001147	small testis	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0031356	abnormal outer dense fiber morphology	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0009230	abnormal sperm head morphology	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0001925	male infertility	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0004852	decreased testis weight	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0014052	increased male germ cell apoptosis	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0002675	asthenozoospermia	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0004929	decreased epididymis weight	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0002687	oligozoospermia	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0001932	abnormal spermiogenesis	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0009834	abnormal sperm annulus morphology	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0009232	abnormal sperm nucleus morphology	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0008892	abnormal sperm flagellum morphology	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0009831	abnormal sperm midpiece morphology	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0005578	teratozoospermia	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0020451	decreased sperm progressive motility	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488110	M	MP:0009833	absent sperm mitochondrial sheath	Actl7b<tm1(KOMP)Vlcg>/Actl7b<tm1(KOMP)Vlcg>	C57BL/6N-Actl7b<tm1(KOMP)Vlcg>	N	36617158
MGI:7488472	M	MP:0002118	abnormal lipid homeostasis	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	N	29093267
MGI:7488472	M	MP:0003402	decreased liver weight	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	N	29093267
MGI:7488472	M	MP:0005286	decreased saturated fatty acids level	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	N	29093267
MGI:7488472	M	MP:0020868	decreased lipogenesis	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	N	29093267
MGI:7488472	M	MP:0005266	abnormal metabolism	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	N	29093267
MGI:7488472	M	MP:0011075	abnormal macrophage activation involved in immune response	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	N	29093267
MGI:7488472	M	MP:0005378	growth/size/body region phenotype	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	Y	29093267
MGI:7488472	M	MP:0009356	decreased liver triglyceride level	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	N	29093267
MGI:7488472	M	MP:0004789	increased bile salt level	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	N	29093267
MGI:7488472	M	MP:0004777	abnormal phospholipid level	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	N	29093267
MGI:7488472	M	MP:0013245	abnormal lipid metabolism	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	N	29093267
MGI:7488472	M	MP:0009823	abnormal sphingomyelin level	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	N	29093267
MGI:7488472	M	MP:0013278	decreased fasting circulating glucose level	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	N	29093267
MGI:7488472	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Mirc13<tm1.1Mtm>/Mirc13<tm1.1Mtm>	Not Specified	N	29093267
MGI:7489810	M	MP:0001363	increased anxiety-related response	Smc3<tm1.2Toshi>/Smc3<+>	B6.Cg-Smc3<tm1.2Toshi>	N	28408410
MGI:7489810	M	MP:0001399	hyperactivity	Smc3<tm1.2Toshi>/Smc3<+>	B6.Cg-Smc3<tm1.2Toshi>	N	28408410
MGI:7489810	M	MP:0005386	behavior/neurological phenotype	Smc3<tm1.2Toshi>/Smc3<+>	B6.Cg-Smc3<tm1.2Toshi>	Y	28408410
MGI:7489855	M	MP:0001363	increased anxiety-related response	Smc3<tm1.1Toshi>/Smc3<+>,Mapt<tm2(cre)Aha>/Mapt<+>	involves: C57BL/6J	N	28408410
MGI:7491684	M	MP:0001544	abnormal cardiovascular system physiology	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491684	M	MP:0001925	male infertility	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491684	M	MP:0001262	decreased body weight	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491684	M	MP:0005376	homeostasis/metabolism phenotype	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	Y	33890822
MGI:7491684	M	MP:0009289	decreased epididymal fat pad weight	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491684	M	MP:0005384	cellular phenotype	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	Y	33890822
MGI:7491684	M	MP:0031358	decreased urine output	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491684	M	MP:0005386	behavior/neurological phenotype	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	Y	33890822
MGI:7491684	M	MP:0009764	decreased susceptibility to induced morbidity/mortality	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491684	M	MP:0003918	decreased kidney weight	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491684	M	MP:0011951	increased cardiac stroke volume	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491684	M	MP:0003960	increased lean body mass	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491684	M	MP:0003402	decreased liver weight	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491684	M	MP:0003915	increased heart left ventricle weight	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491684	M	MP:0012046	decreased susceptibility to hypertension	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491684	M	MP:0006376	decreased circulating angiotensinogen level	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491684	M	MP:0005378	growth/size/body region phenotype	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	Y	33890822
MGI:7491684	M	MP:0005385	cardiovascular system phenotype	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	Y	33890822
MGI:7491684	M	MP:0006264	decreased systemic arterial systolic blood pressure	Atp6ap2<em1Nira>/Y	C57BL/6J-Atp6ap2<em1Nira>	N	33890822
MGI:7491811	F	MP:0001923	reduced female fertility	Inha<em1Crah>/Inha<em1Crah>	involves: C57BL/6J	N	35255139
MGI:7491811	F	MP:0011124	increased primary ovarian follicle number	Inha<em1Crah>/Inha<em1Crah>	involves: C57BL/6J	N	35255139
MGI:7491811	F	MP:0003718	maternal effect	Inha<em1Crah>/Inha<em1Crah>	involves: C57BL/6J	N	35255139
MGI:7491811	F	MP:0031421	increased superovulation rate	Inha<em1Crah>/Inha<em1Crah>	involves: C57BL/6J	N	35255139
MGI:7491811	M	MP:0005389	reproductive system phenotype	Inha<em1Crah>/Inha<em1Crah>	involves: C57BL/6J	Y	35255139
MGI:7491811	F	MP:0005379	endocrine/exocrine gland phenotype	Inha<em1Crah>/Inha<em1Crah>	involves: C57BL/6J	Y	35255139
MGI:7491811	F	MP:0031411	increased ovulation rate	Inha<em1Crah>/Inha<em1Crah>	involves: C57BL/6J	N	35255139
MGI:7491811	F	MP:0001125	abnormal oocyte morphology	Inha<em1Crah>/Inha<em1Crah>	involves: C57BL/6J	N	35255139
MGI:7491811	F	MP:0004904	increased uterus weight	Inha<em1Crah>/Inha<em1Crah>	involves: C57BL/6J	N	35255139
MGI:7491811	F	MP:0004855	increased ovary weight	Inha<em1Crah>/Inha<em1Crah>	involves: C57BL/6J	N	35255139
MGI:7491811	F	MP:0005376	homeostasis/metabolism phenotype	Inha<em1Crah>/Inha<em1Crah>	involves: C57BL/6J	Y	35255139
MGI:7491814	F	MP:0004855	increased ovary weight	Inha<em1Crah>/Inha<+>	C57BL/6J-Inha<em1Crah>	N	35255139
MGI:7491814	F	MP:0005389	reproductive system phenotype	Inha<em1Crah>/Inha<+>	C57BL/6J-Inha<em1Crah>	Y	35255139
MGI:7491814	F	MP:0003718	maternal effect	Inha<em1Crah>/Inha<+>	C57BL/6J-Inha<em1Crah>	N	35255139
MGI:7491814	F	MP:0001934	increased litter size	Inha<em1Crah>/Inha<+>	C57BL/6J-Inha<em1Crah>	N	35255139
MGI:7491814	F	MP:0005376	homeostasis/metabolism phenotype	Inha<em1Crah>/Inha<+>	C57BL/6J-Inha<em1Crah>	Y	35255139
MGI:7491814	F	MP:0031411	increased ovulation rate	Inha<em1Crah>/Inha<+>	C57BL/6J-Inha<em1Crah>	N	35255139
MGI:7491814	F	MP:0031424	enhanced female fertility	Inha<em1Crah>/Inha<+>	C57BL/6J-Inha<em1Crah>	N	35255139
MGI:7491814	F	MP:0005379	endocrine/exocrine gland phenotype	Inha<em1Crah>/Inha<+>	C57BL/6J-Inha<em1Crah>	Y	35255139
MGI:7491951	M	MP:0010038	abnormal placenta physiology	Hdac8<tm1.2Eno>/Y	involves: 129S6/SvEvTac * C57BL/6J	N	32800293
MGI:7491951	M	MP:0009429	decreased embryo weight	Hdac8<tm1.2Eno>/Y	involves: 129S6/SvEvTac * C57BL/6J	N	32800293
MGI:7491951	M	MP:0011086	postnatal lethality, incomplete penetrance	Hdac8<tm1.2Eno>/Y	involves: 129S6/SvEvTac * C57BL/6J	N	32800293
MGI:7491951	M	MP:0004023	abnormal chromosome number	Hdac8<tm1.2Eno>/Y	involves: 129S6/SvEvTac * C57BL/6J	N	32800293
MGI:7491951	M	MP:0004920	increased placenta weight	Hdac8<tm1.2Eno>/Y	involves: 129S6/SvEvTac * C57BL/6J	N	32800293
MGI:7491951	M	MP:0014321	short forelimb	Hdac8<tm1.2Eno>/Y	involves: 129S6/SvEvTac * C57BL/6J	N	32800293
MGI:7491951	M	MP:0008058	abnormal DNA repair	Hdac8<tm1.2Eno>/Y	involves: 129S6/SvEvTac * C57BL/6J	N	32800293
MGI:7491951	M	MP:0008959	abnormal spongiotrophoblast cell morphology	Hdac8<tm1.2Eno>/Y	involves: 129S6/SvEvTac * C57BL/6J	N	32800293
MGI:7491951	M	MP:0008957	abnormal placenta junctional zone morphology	Hdac8<tm1.2Eno>/Y	involves: 129S6/SvEvTac * C57BL/6J	N	32800293
MGI:7491953	M	MP:0011086	postnatal lethality, incomplete penetrance	Eif2ak2<tm1Cwe>/Eif2ak2<tm1Cwe>,Hdac8<tm1.2Eno>/Y	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J	N	32800293
MGI:7491953	M	MP:0002109	abnormal limb morphology	Eif2ak2<tm1Cwe>/Eif2ak2<tm1Cwe>,Hdac8<tm1.2Eno>/Y	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J	N	32800293
MGI:7492024	M	MP:0010869	decreased bone trabecula number	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0004985	decreased osteoclast cell number	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0013630	increased bone trabecular spacing	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0000458	abnormal mandible morphology	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0020039	increased bone ossification	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0011642	abnormal bone collagen fibril morphology	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0001541	abnormal osteoclast physiology	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0030050	large mandible	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0009346	decreased trabecular bone thickness	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0004148	increased compact bone thickness	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0011710	enhanced osteoblast differentiation	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0004991	decreased bone strength	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0010932	increased trabecular bone connectivity density	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0000062	increased bone mineral density	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0005190	osteomyelitis	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0010123	increased bone mineral content	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0004358	bowed tibia	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492024	M	MP:0005422	osteosclerosis	Ano5<em2Huyi>/Ano5<em2Huyi>	C57BL/6-Ano5<em2Huyi>	N	34841576
MGI:7492275	M	MP:0001399	hyperactivity	Cul3<em1Limi>/Cul3<+>	C57BL/6N-Cul3<em1Limi>	N	33727673
MGI:7493591	F	MP:0002636	delayed vaginal opening	Chd7<Gt(S20-7E1)Sor>/Chd7<+>	129S1.129S4(B6)-Chd7<Gt(S20-7E1)Sor>	N	21596839
MGI:7493591	F	MP:0001938	delayed sexual maturation	Chd7<Gt(S20-7E1)Sor>/Chd7<+>	129S1.129S4(B6)-Chd7<Gt(S20-7E1)Sor>	N	21596839
MGI:7493591	F	MP:0009008	delayed estrous cycle	Chd7<Gt(S20-7E1)Sor>/Chd7<+>	129S1.129S4(B6)-Chd7<Gt(S20-7E1)Sor>	N	21596839
MGI:7493591	F	MP:0002790	decreased circulating follicle stimulating hormone level	Chd7<Gt(S20-7E1)Sor>/Chd7<+>	129S1.129S4(B6)-Chd7<Gt(S20-7E1)Sor>	N	21596839
MGI:7493591	F	MP:0001927	abnormal estrous cycle	Chd7<Gt(S20-7E1)Sor>/Chd7<+>	129S1.129S4(B6)-Chd7<Gt(S20-7E1)Sor>	N	21596839
MGI:7494375	M	MP:0006097	abnormal cerebellar lobule formation	Chd7<tm2c(EUCOMM)Wtsi>/Chd7<tm2c(EUCOMM)Wtsi>,Tg(Atoh1-cre)1Bfri/0,Tg(Nes-Reln)#Cur/0	involves: C57BL/6 * C57BL/6J * C57BL/6N * CBA * FVB	N	28165338
MGI:7506440	F	MP:0005389	reproductive system phenotype	Ct55<em2Xdzg>/Ct55<em2Xdzg>	C57BL/6-Ct55<em2Xdzg>	Y	36481789
MGI:7506441	M	MP:0006380	abnormal spermatid morphology	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0008995	early reproductive senescence	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0004543	abnormal sperm physiology	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0011743	abnormal Golgi apparatus morphology	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0002675	asthenozoospermia	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0031372	abnormal sperm individualization	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0001925	male infertility	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0005389	reproductive system phenotype	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	Y	36481789
MGI:7506441	M	MP:0030590	abnormal sperm fibrous sheath morphology	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0008898	abnormal acrosome morphology	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0002687	oligozoospermia	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0030940	impaired autophagy	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0002631	abnormal epididymis morphology	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0001156	abnormal spermatogenesis	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0020451	decreased sperm progressive motility	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0031354	abnormal acrosome assembly	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0009647	decreased fertilization frequency	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506441	M	MP:0001932	abnormal spermiogenesis	Ct55<em2Xdzg>/Y	C57BL/6-Ct55<em2Xdzg>	N	36481789
MGI:7506549	M	MP:0004884	abnormal testis physiology	Frey1<em1Osb>/Frey1<em1Osb>	involves: C57BL/6 * DBA/2	N	36787362
MGI:7506549	M	MP:0004543	abnormal sperm physiology	Frey1<em1Osb>/Frey1<em1Osb>	involves: C57BL/6 * DBA/2	N	36787362
MGI:7506549	M	MP:0001922	reduced male fertility	Frey1<em1Osb>/Frey1<em1Osb>	involves: C57BL/6 * DBA/2	N	36787362
MGI:7506549	M	MP:0031010	failure of sperm-egg fusion	Frey1<em1Osb>/Frey1<em1Osb>	involves: C57BL/6 * DBA/2	N	36787362
MGI:7506549	M	MP:0000242	impaired fertilization	Frey1<em1Osb>/Frey1<em1Osb>	involves: C57BL/6 * DBA/2	N	36787362
MGI:7506565	M	MP:0005389	reproductive system phenotype	Frey1<em1Osb>/Frey1<em1Osb>,Tg(Clgn-Frey1)1Osb/0	involves: C57BL/6 * DBA/2	Y	36787362
MGI:7506568	M	MP:0005389	reproductive system phenotype	Frey1<tm2Osb>/Frey1<tm2Osb>	C57BL/6J-Frey1<tm2Osb>	Y	36787362
MGI:7506568	M	MP:0001925	male infertility	Frey1<tm2Osb>/Frey1<tm2Osb>	C57BL/6J-Frey1<tm2Osb>	N	36787362
MGI:7506935	M	MP:0001156	abnormal spermatogenesis	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0001154	seminiferous tubule degeneration	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0009831	abnormal sperm midpiece morphology	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0009376	abnormal manchette morphology	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0004182	abnormal spermiation	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0008898	abnormal acrosome morphology	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0005578	teratozoospermia	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0001925	male infertility	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0009230	abnormal sperm head morphology	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0002687	oligozoospermia	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0011750	abnormal seminiferous tubule epithelium morphology	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0009231	detached acrosome	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0020362	abnormal male germ cell physiology	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0006362	abnormal male germ cell morphology	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7506935	M	MP:0001932	abnormal spermiogenesis	Tssk3<em1Osb>/Tssk3<em1Osb>	involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2	N	36306217
MGI:7507024	M	MP:0001925	male infertility	Adad2<em1Osb>/Adad2<em1Osb>	involves: C57BL/6 * DBA/2	N	36698249
MGI:7507024	M	MP:0006379	abnormal spermatocyte morphology	Adad2<em1Osb>/Adad2<em1Osb>	involves: C57BL/6 * DBA/2	N	36698249
MGI:7507024	M	MP:0006380	abnormal spermatid morphology	Adad2<em1Osb>/Adad2<em1Osb>	involves: C57BL/6 * DBA/2	N	36698249
MGI:7507024	M	MP:0004901	decreased male germ cell number	Adad2<em1Osb>/Adad2<em1Osb>	involves: C57BL/6 * DBA/2	N	36698249
MGI:7507024	M	MP:0001156	abnormal spermatogenesis	Adad2<em1Osb>/Adad2<em1Osb>	involves: C57BL/6 * DBA/2	N	36698249
MGI:7507024	M	MP:0009230	abnormal sperm head morphology	Adad2<em1Osb>/Adad2<em1Osb>	involves: C57BL/6 * DBA/2	N	36698249
MGI:7507024	M	MP:0005389	reproductive system phenotype	Adad2<em1Osb>/Adad2<em1Osb>	involves: C57BL/6 * DBA/2	Y	36698249
MGI:7507024	M	MP:0005169	abnormal male meiosis	Adad2<em1Osb>/Adad2<em1Osb>	involves: C57BL/6 * DBA/2	N	36698249
MGI:7507024	M	MP:0001932	abnormal spermiogenesis	Adad2<em1Osb>/Adad2<em1Osb>	involves: C57BL/6 * DBA/2	N	36698249
MGI:7507026	M	MP:0014052	increased male germ cell apoptosis	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7507026	M	MP:0006378	abnormal spermatogonia morphology	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7507026	M	MP:0004852	decreased testis weight	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7507026	M	MP:0009451	abnormal chromosomal synapsis	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7507026	M	MP:0004901	decreased male germ cell number	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7507026	M	MP:0001156	abnormal spermatogenesis	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7507026	M	MP:0002216	abnormal seminiferous tubule morphology	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7507026	M	MP:0001155	arrest of spermatogenesis	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7507026	M	MP:0012167	abnormal epigenetic regulation of gene expression	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7507026	M	MP:0005159	azoospermia	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7507026	M	MP:0005389	reproductive system phenotype	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	Y	35918532
MGI:7507026	M	MP:0001940	testis hypoplasia	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7507026	M	MP:0008898	abnormal acrosome morphology	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7507026	M	MP:0001925	male infertility	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7507026	M	MP:0008261	arrest of male meiosis	Cxxc1<tm2.1Skk>/Cxxc1<tm2.1Skk>,Tg(Stra8-icre)1Reb/0	involves: FVB/NJ	N	35918532
MGI:7509141	F	MP:0005389	reproductive system phenotype	Dis3l2<em1Dean>/Dis3l2<em1Dean>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J * DBA/2	Y	36727488
MGI:7509141	F	MP:0001926	female infertility	Dis3l2<em1Dean>/Dis3l2<em1Dean>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J * DBA/2	N	36727488
MGI:7509141	F	MP:0005168	abnormal female meiosis	Dis3l2<em1Dean>/Dis3l2<em1Dean>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J * DBA/2	N	36727488
MGI:7509141	F	MP:0001125	abnormal oocyte morphology	Dis3l2<em1Dean>/Dis3l2<em1Dean>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J * DBA/2	N	36727488
MGI:7509141	F	MP:0013272	abnormal translation	Dis3l2<em1Dean>/Dis3l2<em1Dean>,Tg(Zp3-cre)93Knw/0	involves: C57BL/6 * C57BL/6J * DBA/2	N	36727488
MGI:7509348	M	MP:0010948	abnormal double-strand DNA break repair	Elp1<tm1c(KOMP)Wtsi>/Elp1<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6N * FVB	N	23717213
MGI:7509348	M	MP:0001147	small testis	Elp1<tm1c(KOMP)Wtsi>/Elp1<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6N * FVB	N	23717213
MGI:7509348	M	MP:0008261	arrest of male meiosis	Elp1<tm1c(KOMP)Wtsi>/Elp1<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6N * FVB	N	23717213
MGI:7509348	M	MP:0005159	azoospermia	Elp1<tm1c(KOMP)Wtsi>/Elp1<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6N * FVB	N	23717213
MGI:7509348	M	MP:0001925	male infertility	Elp1<tm1c(KOMP)Wtsi>/Elp1<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6N * FVB	N	23717213
MGI:7509348	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Elp1<tm1c(KOMP)Wtsi>/Elp1<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6N * FVB	N	23717213
MGI:7509348	M	MP:0009451	abnormal chromosomal synapsis	Elp1<tm1c(KOMP)Wtsi>/Elp1<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6N * FVB	N	23717213
MGI:7509348	M	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome	Elp1<tm1c(KOMP)Wtsi>/Elp1<tm1c(KOMP)Wtsi>,Tg(Ddx4-cre)1Dcas/0	involves: 129 * C57BL/6N * FVB	N	23717213
MGI:7509435	M	MP:0001925	male infertility	Adad1<em1Osb>/Adad1<em1Osb>	involves: C57BL/6 * DBA/2	N	36698249
MGI:7509435	M	MP:0001932	abnormal spermiogenesis	Adad1<em1Osb>/Adad1<em1Osb>	involves: C57BL/6 * DBA/2	N	36698249
MGI:7509464	M	MP:0004901	decreased male germ cell number	Adad2<em2Osb>/Adad2<em2Osb>	C57BL/6J-Adad2<em2Osb>	N	36698249
MGI:7509464	M	MP:0001156	abnormal spermatogenesis	Adad2<em2Osb>/Adad2<em2Osb>	C57BL/6J-Adad2<em2Osb>	N	36698249
MGI:7509464	M	MP:0020550	multinucleated giant male germ cells	Adad2<em2Osb>/Adad2<em2Osb>	C57BL/6J-Adad2<em2Osb>	N	36698249
MGI:7509464	M	MP:0001925	male infertility	Adad2<em2Osb>/Adad2<em2Osb>	C57BL/6J-Adad2<em2Osb>	N	36698249
MGI:7509464	M	MP:0004852	decreased testis weight	Adad2<em2Osb>/Adad2<em2Osb>	C57BL/6J-Adad2<em2Osb>	N	36698249
MGI:7509464	M	MP:0008279	arrest of spermiogenesis	Adad2<em2Osb>/Adad2<em2Osb>	C57BL/6J-Adad2<em2Osb>	N	36698249
MGI:7509544	M	MP:0031633	decreased heart left ventricle muscle contractility	Csrp3<tm1.1Kage>/Csrp3<tm1.1Kage>	involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	30048712
MGI:7509544	M	MP:0002833	increased heart weight	Csrp3<tm1.1Kage>/Csrp3<tm1.1Kage>	involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	30048712
MGI:7509544	M	MP:0010579	increased heart left ventricle size	Csrp3<tm1.1Kage>/Csrp3<tm1.1Kage>	involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	30048712
MGI:7509544	M	MP:0004084	abnormal cardiac muscle relaxation	Csrp3<tm1.1Kage>/Csrp3<tm1.1Kage>	involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	30048712
MGI:7509544	M	MP:0003915	increased heart left ventricle weight	Csrp3<tm1.1Kage>/Csrp3<tm1.1Kage>	involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL	N	30048712
MGI:7511578	F	MP:0002678	increased follicle recruitment	Ptk2b<em1Yank>/Ptk2b<em1Yank>	Not Specified	N	32608523
MGI:7511578	F	MP:0001934	increased litter size	Ptk2b<em1Yank>/Ptk2b<em1Yank>	Not Specified	N	32608523
MGI:7511587	F	MP:0005389	reproductive system phenotype	Ptk2b<em2Yank>/Ptk2b<em2Yank>	Not Specified	Y	32608523
MGI:7511679	M	MP:0009831	abnormal sperm midpiece morphology	Tsks<em1Osb>/Tsks<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	36881620
MGI:7511679	M	MP:0001925	male infertility	Tsks<em1Osb>/Tsks<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	36881620
MGI:7511679	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Tsks<em1Osb>/Tsks<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	36881620
MGI:7511679	M	MP:0005389	reproductive system phenotype	Tsks<em1Osb>/Tsks<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	Y	36881620
MGI:7511679	M	MP:0004182	abnormal spermiation	Tsks<em1Osb>/Tsks<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	36881620
MGI:7511679	M	MP:0020451	decreased sperm progressive motility	Tsks<em1Osb>/Tsks<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	36881620
MGI:7511679	M	MP:0005578	teratozoospermia	Tsks<em1Osb>/Tsks<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	36881620
MGI:7511679	M	MP:0001156	abnormal spermatogenesis	Tsks<em1Osb>/Tsks<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	36881620
MGI:7511679	M	MP:0002675	asthenozoospermia	Tsks<em1Osb>/Tsks<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	36881620
MGI:7511679	M	MP:0006380	abnormal spermatid morphology	Tsks<em1Osb>/Tsks<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	36881620
MGI:7511679	M	MP:0009230	abnormal sperm head morphology	Tsks<em1Osb>/Tsks<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	36881620
MGI:7511679	M	MP:0014052	increased male germ cell apoptosis	Tsks<em1Osb>/Tsks<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	36881620
MGI:7511679	M	MP:0009647	decreased fertilization frequency	Tsks<em1Osb>/Tsks<em1Osb>	involves: 129S2/SvPas * C57BL/6NSlc	N	36881620
MGI:7511762	M	MP:0020451	decreased sperm progressive motility	Tmem232<em1Shliu>/Tmem232<em1Shliu>	C57BL/6-Tmem232<em1Shliu>	N	37371084
MGI:7511762	M	MP:0001925	male infertility	Tmem232<em1Shliu>/Tmem232<em1Shliu>	C57BL/6-Tmem232<em1Shliu>	N	37371084
MGI:7511762	M	MP:0009243	hairpin sperm flagellum	Tmem232<em1Shliu>/Tmem232<em1Shliu>	C57BL/6-Tmem232<em1Shliu>	N	37371084
MGI:7511762	M	MP:0009838	abnormal sperm axoneme morphology	Tmem232<em1Shliu>/Tmem232<em1Shliu>	C57BL/6-Tmem232<em1Shliu>	N	37371084
MGI:7511762	M	MP:0031356	abnormal outer dense fiber morphology	Tmem232<em1Shliu>/Tmem232<em1Shliu>	C57BL/6-Tmem232<em1Shliu>	N	37371084
MGI:7511762	M	MP:0002687	oligozoospermia	Tmem232<em1Shliu>/Tmem232<em1Shliu>	C57BL/6-Tmem232<em1Shliu>	N	37371084
MGI:7511762	M	MP:0030590	abnormal sperm fibrous sheath morphology	Tmem232<em1Shliu>/Tmem232<em1Shliu>	C57BL/6-Tmem232<em1Shliu>	N	37371084
MGI:7511762	M	MP:0008892	abnormal sperm flagellum morphology	Tmem232<em1Shliu>/Tmem232<em1Shliu>	C57BL/6-Tmem232<em1Shliu>	N	37371084
MGI:7511762	M	MP:0002675	asthenozoospermia	Tmem232<em1Shliu>/Tmem232<em1Shliu>	C57BL/6-Tmem232<em1Shliu>	N	37371084
MGI:7511828	F	MP:0001552	increased circulating triglyceride level	Apoe<tm1Unc>/Apoe<tm1Unc>,Atic<tm1c(EUCOMM)Hmgu>/Atic<tm1c(EUCOMM)Hmgu>,Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J * C57BL/6N	N	36073366
MGI:7511828	M	MP:0005179	decreased circulating cholesterol level	Apoe<tm1Unc>/Apoe<tm1Unc>,Atic<tm1c(EUCOMM)Hmgu>/Atic<tm1c(EUCOMM)Hmgu>,Gt(ROSA)26Sor<tm1(cre/ERT2)Tyj>/Gt(ROSA)26Sor<+>	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J * C57BL/6N	N	36073366
MGI:7513944	M	MP:0008892	abnormal sperm flagellum morphology	Kpna2<em1Alfon>/Kpna2<em1Alfon>	involves: C57BL/6 * CBA	N	37456838
MGI:7513944	M	MP:0001925	male infertility	Kpna2<em1Alfon>/Kpna2<em1Alfon>	involves: C57BL/6 * CBA	N	37456838
MGI:7513944	M	MP:0009831	abnormal sperm midpiece morphology	Kpna2<em1Alfon>/Kpna2<em1Alfon>	involves: C57BL/6 * CBA	N	37456838
MGI:7513944	M	MP:0009230	abnormal sperm head morphology	Kpna2<em1Alfon>/Kpna2<em1Alfon>	involves: C57BL/6 * CBA	N	37456838
MGI:7513944	M	MP:0002675	asthenozoospermia	Kpna2<em1Alfon>/Kpna2<em1Alfon>	involves: C57BL/6 * CBA	N	37456838
MGI:7513944	M	MP:0020451	decreased sperm progressive motility	Kpna2<em1Alfon>/Kpna2<em1Alfon>	involves: C57BL/6 * CBA	N	37456838
MGI:7513944	M	MP:0005578	teratozoospermia	Kpna2<em1Alfon>/Kpna2<em1Alfon>	involves: C57BL/6 * CBA	N	37456838
MGI:7514248	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	M	MP:0001922	reduced male fertility	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	M	MP:0002687	oligozoospermia	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	M	MP:0008967	absent chiasmata formation	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	M	MP:0001154	seminiferous tubule degeneration	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	M	MP:0009451	abnormal chromosomal synapsis	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	M	MP:0005169	abnormal male meiosis	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	M	MP:0014052	increased male germ cell apoptosis	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	F	MP:0005389	reproductive system phenotype	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	Y	35712867
MGI:7514248	M	MP:0001156	abnormal spermatogenesis	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	M	MP:0009452	abnormal synaptonemal complex	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	M	MP:0008261	arrest of male meiosis	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	M	MP:0020550	multinucleated giant male germ cells	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	M	MP:0004901	decreased male germ cell number	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	M	MP:0001935	decreased litter size	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514248	M	MP:0001147	small testis	Mir202<em1Hncs>/Mir202<em1Hncs>	involves: C57BL/6J * ICR	N	35712867
MGI:7514535	M	MP:0004564	increased myocardial fiber size	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0031131	myocardial fiber disarray	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0003953	abnormal hormone level	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0000278	abnormal myocardial fiber morphology	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0010724	thick interventricular septum	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0006035	abnormal mitochondrial morphology	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0021157	increased heart left ventricle wall thickness	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0005140	decreased cardiac muscle contractility	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0010633	myocardium hypertrophy	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0021161	increased heart left ventricle posterior wall thickness	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0004485	increased response of heart to induced stress	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0011632	dilated mitochondrion	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0000274	enlarged heart	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0005599	increased cardiac muscle contractility	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514535	M	MP:0001625	cardiac hypertrophy	Cmtm3<em1Wlh>/Cmtm3<em1Wlh>	involves: C57BL/6	N	37229825
MGI:7514571	M	MP:0001153	small seminiferous tubules	Zfp541<em1Fcw>/Zfp541<em1Fcw>	Not Specified	N	35341968
MGI:7514571	M	MP:0010948	abnormal double-strand DNA break repair	Zfp541<em1Fcw>/Zfp541<em1Fcw>	Not Specified	N	35341968
MGI:7514571	M	MP:0014052	increased male germ cell apoptosis	Zfp541<em1Fcw>/Zfp541<em1Fcw>	Not Specified	N	35341968
MGI:7514571	M	MP:0001156	abnormal spermatogenesis	Zfp541<em1Fcw>/Zfp541<em1Fcw>	Not Specified	N	35341968
MGI:7514571	M	MP:0008261	arrest of male meiosis	Zfp541<em1Fcw>/Zfp541<em1Fcw>	Not Specified	N	35341968
MGI:7514571	M	MP:0005159	azoospermia	Zfp541<em1Fcw>/Zfp541<em1Fcw>	Not Specified	N	35341968
MGI:7514571	M	MP:0001147	small testis	Zfp541<em1Fcw>/Zfp541<em1Fcw>	Not Specified	N	35341968
MGI:7514571	M	MP:0001925	male infertility	Zfp541<em1Fcw>/Zfp541<em1Fcw>	Not Specified	N	35341968
MGI:7514571	M	MP:0005169	abnormal male meiosis	Zfp541<em1Fcw>/Zfp541<em1Fcw>	Not Specified	N	35341968
MGI:7514571	M	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis	Zfp541<em1Fcw>/Zfp541<em1Fcw>	Not Specified	N	35341968
MGI:7514571	M	MP:0006379	abnormal spermatocyte morphology	Zfp541<em1Fcw>/Zfp541<em1Fcw>	Not Specified	N	35341968
MGI:7514989	M	MP:0005316	abnormal response to tactile stimuli	Tmem160<em1.1Bros>/Tmem160<em1.1Bros>	involves: C57BL/6JRj * FVB/N	N	34936870
MGI:7514989	M	MP:0008713	abnormal cytokine level	Tmem160<em1.1Bros>/Tmem160<em1.1Bros>	involves: C57BL/6JRj * FVB/N	N	34936870
MGI:7514989	M	MP:0004811	abnormal neuron physiology	Tmem160<em1.1Bros>/Tmem160<em1.1Bros>	involves: C57BL/6JRj * FVB/N	N	34936870
MGI:7514989	M	MP:0001442	decreased grooming behavior	Tmem160<em1.1Bros>/Tmem160<em1.1Bros>	involves: C57BL/6JRj * FVB/N	N	34936870
MGI:7514991	M	MP:0005386	behavior/neurological phenotype	Tg(Avil-cre)1Phep/0,Tmem160<em1Bros>/Tmem160<em1Bros>	involves: C57BL/6 * C57BL/6JRj * DBA/2	Y	34936870
MGI:7514991	M	MP:0005376	homeostasis/metabolism phenotype	Tg(Avil-cre)1Phep/0,Tmem160<em1Bros>/Tmem160<em1Bros>	involves: C57BL/6 * C57BL/6JRj * DBA/2	Y	34936870
MGI:7516682	F	MP:0005577	uterus prolapse	Loxl1<em1Andm>/Loxl1<em1Andm>	C57BL/6J-Loxl1<em1Andm>	N	MGI:7516676
MGI:7516685	F	MP:0005577	uterus prolapse	Loxl1<em2Andm>/Loxl1<em2Andm>	C57BL/6J-Loxl1<em2Andm>	N	MGI:7516676
MGI:7516688	F	MP:0005577	uterus prolapse	Loxl1<em3Andm>/Loxl1<em3Andm>	C57BL/6J-Loxl1<em3Andm>	N	MGI:7516676
MGI:7516691	F	MP:0005577	uterus prolapse	Loxl1<em4Andm>/Loxl1<em4Andm>	C57BL/6J-Loxl1<em4Andm>	N	MGI:7516676
MGI:7516693	F	MP:0005577	uterus prolapse	Loxl1<em5Andm>/Loxl1<em5Andm>	C57BL/6J-Loxl1<em5Andm>	N	MGI:7516676
MGI:7516760	M	MP:0005389	reproductive system phenotype	Mageb4<em1Zhpw>/0	involves: C57BL/6 * DBA/2J	Y	37451217
MGI:7516761	M	MP:0005389	reproductive system phenotype	Mageb4<em2Zhpw>/0	involves: C57BL/6 * DBA/2J	N	37451217
MGI:7517013	M	MP:0003999	enhanced passive avoidance behavior	Septin14<em1.1Plk>/Septin14<em1.1Plk>	involves: C57BL/6 * CBA	N	35571367
MGI:7517090	M	MP:0000559	abnormal femur morphology	Rab33b<em1Rmr>/Rab33b<em1Rmr>	involves: C57BL/6	N	37359363
MGI:7517090	M	MP:0004982	abnormal osteoclast morphology	Rab33b<em1Rmr>/Rab33b<em1Rmr>	involves: C57BL/6	N	37359363
MGI:7517090	M	MP:0013625	increased femur yield load	Rab33b<em1Rmr>/Rab33b<em1Rmr>	involves: C57BL/6	N	37359363
MGI:7517090	M	MP:0004984	increased osteoclast cell number	Rab33b<em1Rmr>/Rab33b<em1Rmr>	involves: C57BL/6	N	37359363
MGI:7517090	M	MP:0001262	decreased body weight	Rab33b<em1Rmr>/Rab33b<em1Rmr>	involves: C57BL/6	N	37359363
MGI:7517090	M	MP:0004148	increased compact bone thickness	Rab33b<em1Rmr>/Rab33b<em1Rmr>	involves: C57BL/6	N	37359363
MGI:7517091	M	MP:0008396	abnormal osteoclast differentiation	Rab33b<em1Rmr>/Rab33b<+>	involves: C57BL/6	N	37359363
MGI:7517091	M	MP:0021191	increased bone mineral density of lumbar vertebrae	Rab33b<em1Rmr>/Rab33b<+>	involves: C57BL/6	N	37359363
MGI:7517091	M	MP:0013637	increased femur stiffness	Rab33b<em1Rmr>/Rab33b<+>	involves: C57BL/6	N	37359363
MGI:7517091	M	MP:0013625	increased femur yield load	Rab33b<em1Rmr>/Rab33b<+>	involves: C57BL/6	N	37359363
MGI:7517091	M	MP:0013623	increased femur compact bone thickness	Rab33b<em1Rmr>/Rab33b<+>	involves: C57BL/6	N	37359363
MGI:7517091	M	MP:0004982	abnormal osteoclast morphology	Rab33b<em1Rmr>/Rab33b<+>	involves: C57BL/6	N	37359363
MGI:7517091	M	MP:0004993	decreased bone resorption	Rab33b<em1Rmr>/Rab33b<+>	involves: C57BL/6	N	37359363
MGI:7517091	M	MP:0009347	increased trabecular bone thickness	Rab33b<em1Rmr>/Rab33b<+>	involves: C57BL/6	N	37359363
MGI:7517091	M	MP:0004984	increased osteoclast cell number	Rab33b<em1Rmr>/Rab33b<+>	involves: C57BL/6	N	37359363
MGI:7517091	M	MP:0013615	increased volumetric bone mineral density	Rab33b<em1Rmr>/Rab33b<+>	involves: C57BL/6	N	37359363
MGI:7518590	M	MP:0002941	increased circulating alanine transaminase level	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0009302	increased renal fat pad weight	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0000182	increased circulating LDL cholesterol level	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0001260	increased body weight	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0005293	impaired glucose tolerance	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0014170	increased brown adipose tissue mass	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0005178	increased circulating cholesterol level	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0009286	increased abdominal fat pad weight	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0014146	decreased white adipose tissue mass	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0002628	hepatic steatosis	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0005331	insulin resistance	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0005343	increased circulating aspartate transaminase level	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0002968	increased circulating alkaline phosphatase level	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0009355	increased liver triglyceride level	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0010955	abnormal respiratory electron transport chain	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7518590	M	MP:0005336	abnormal inguinal fat pad morphology	Lmna<em1Fenz>/Lmna<+>	C57BL/6-Lmna<em1Fenz>	N	36583724
MGI:7519037	M	MP:0000774	decreased brain size	Mplkip<em2Nimo>/Mplkip<em2Nimo>	C57BL/6-Mplkip<em2Nimo>	N	37369199
MGI:7520358	M	MP:0010955	abnormal respiratory electron transport chain	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0003921	abnormal heart left ventricle morphology	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0011633	abnormal mitochondrial shape	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0011636	disorganized mitochondrial cristae	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0002083	premature death	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0031633	decreased heart left ventricle muscle contractility	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0010954	abnormal cellular respiration	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0011925	abnormal heart echocardiography feature	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0000274	enlarged heart	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0000266	abnormal heart morphology	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0006036	abnormal mitochondrial physiology	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0031511	globular heart	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0011631	decreased mitochondrial size	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0011628	increased mitochondrial number	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0002795	dilated cardiomyopathy	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0004777	abnormal phospholipid level	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0002753	dilated heart left ventricle	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520358	M	MP:0008770	decreased survivor rate	Tafazzin<em1Xfa>/Y,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520366	F	MP:0011925	abnormal heart echocardiography feature	Tafazzin<em1Xfa>/Tafazzin<em1Xfa>,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520366	F	MP:0031633	decreased heart left ventricle muscle contractility	Tafazzin<em1Xfa>/Tafazzin<em1Xfa>,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7520366	F	MP:0002795	dilated cardiomyopathy	Tafazzin<em1Xfa>/Tafazzin<em1Xfa>,Tg(myl7.L-cre)1118Tmhn/0	involves: C57BL/6NCrl * MF1	N	34129362
MGI:7521958	F	MP:0009769	abnormal meiotic spindle assembly checkpoint	Lsm14b<tm1a(KOMP)Mbp>/Lsm14b<tm1a(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	37083226
MGI:7521958	F	MP:0001125	abnormal oocyte morphology	Lsm14b<tm1a(KOMP)Mbp>/Lsm14b<tm1a(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	37083226
MGI:7521958	M	MP:0005389	reproductive system phenotype	Lsm14b<tm1a(KOMP)Mbp>/Lsm14b<tm1a(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	Y	37083226
MGI:7521958	F	MP:0013272	abnormal translation	Lsm14b<tm1a(KOMP)Mbp>/Lsm14b<tm1a(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	37083226
MGI:7521958	F	MP:0001926	female infertility	Lsm14b<tm1a(KOMP)Mbp>/Lsm14b<tm1a(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	37083226
MGI:7521958	F	MP:0031420	decreased superovulation rate	Lsm14b<tm1a(KOMP)Mbp>/Lsm14b<tm1a(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	37083226
MGI:7521958	F	MP:0009093	oocyte degeneration	Lsm14b<tm1a(KOMP)Mbp>/Lsm14b<tm1a(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	37083226
MGI:7521958	F	MP:0005168	abnormal female meiosis	Lsm14b<tm1a(KOMP)Mbp>/Lsm14b<tm1a(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	37083226
MGI:7521958	F	MP:0001931	abnormal oogenesis	Lsm14b<tm1a(KOMP)Mbp>/Lsm14b<tm1a(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	37083226
MGI:7521958	F	MP:0009647	decreased fertilization frequency	Lsm14b<tm1a(KOMP)Mbp>/Lsm14b<tm1a(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	37083226
MGI:7521958	F	MP:0014443	impaired polar body extrusion	Lsm14b<tm1a(KOMP)Mbp>/Lsm14b<tm1a(KOMP)Mbp>	involves: C57BL/6J * C57BL/6N	N	37083226
MGI:7522223	M	MP:0009237	kinked sperm flagellum	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl<tm1b(KOMP)Wtsi>	N	37607933
MGI:7522223	M	MP:0009831	abnormal sperm midpiece morphology	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl<tm1b(KOMP)Wtsi>	N	37607933
MGI:7522223	M	MP:0020451	decreased sperm progressive motility	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl<tm1b(KOMP)Wtsi>	N	37607933
MGI:7522223	M	MP:0009830	abnormal sperm connecting piece morphology	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl<tm1b(KOMP)Wtsi>	N	37607933
MGI:7522223	M	MP:0005389	reproductive system phenotype	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl<tm1b(KOMP)Wtsi>	Y	37607933
MGI:7522223	M	MP:0014239	abnormal intracellular organelle morphology	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl<tm1b(KOMP)Wtsi>	N	37607933
MGI:7522223	M	MP:0005578	teratozoospermia	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl<tm1b(KOMP)Wtsi>	N	37607933
MGI:7522223	M	MP:0002675	asthenozoospermia	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl<tm1b(KOMP)Wtsi>	N	37607933
MGI:7522223	M	MP:0001932	abnormal spermiogenesis	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl<tm1b(KOMP)Wtsi>	N	37607933
MGI:7522223	M	MP:0001925	male infertility	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl<tm1b(KOMP)Wtsi>	N	37607933
MGI:7522223	M	MP:0001922	reduced male fertility	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl<tm1b(KOMP)Wtsi>	N	37607933
MGI:7522223	M	MP:0008469	abnormal protein level	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl<tm1b(KOMP)Wtsi>	N	37607933
MGI:7522223	M	MP:0009230	abnormal sperm head morphology	Sypl1<tm1b(KOMP)Wtsi>/Sypl1<tm1b(KOMP)Wtsi>	C57BL/6N-Sypl<tm1b(KOMP)Wtsi>	N	37607933
MGI:7524105	M	MP:0001364	decreased anxiety-related response	Abtb3<tm1c(EUCOMM)Wtsi>/Abtb3<tm1c(EUCOMM)Wtsi>,Slc32a1<tm2(cre)Lowl>/Slc32a1<+>	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	N	37261953
MGI:7524327	M	MP:0002216	abnormal seminiferous tubule morphology	Far1<em1(IMPC)Wtsi>/Far1<em1(IMPC)Wtsi>	C57BL/6N-Far1<em1(IMPC)Wtsi>	N	37039784
MGI:7524327	M	MP:0005159	azoospermia	Far1<em1(IMPC)Wtsi>/Far1<em1(IMPC)Wtsi>	C57BL/6N-Far1<em1(IMPC)Wtsi>	N	37039784
MGI:7524327	M	MP:0004901	decreased male germ cell number	Far1<em1(IMPC)Wtsi>/Far1<em1(IMPC)Wtsi>	C57BL/6N-Far1<em1(IMPC)Wtsi>	N	37039784
MGI:7524327	M	MP:0001925	male infertility	Far1<em1(IMPC)Wtsi>/Far1<em1(IMPC)Wtsi>	C57BL/6N-Far1<em1(IMPC)Wtsi>	N	37039784
MGI:7524327	M	MP:0001155	arrest of spermatogenesis	Far1<em1(IMPC)Wtsi>/Far1<em1(IMPC)Wtsi>	C57BL/6N-Far1<em1(IMPC)Wtsi>	N	37039784
MGI:7524327	M	MP:0001156	abnormal spermatogenesis	Far1<em1(IMPC)Wtsi>/Far1<em1(IMPC)Wtsi>	C57BL/6N-Far1<em1(IMPC)Wtsi>	N	37039784
MGI:7524327	M	MP:0001147	small testis	Far1<em1(IMPC)Wtsi>/Far1<em1(IMPC)Wtsi>	C57BL/6N-Far1<em1(IMPC)Wtsi>	N	37039784
MGI:7524327	M	MP:0004852	decreased testis weight	Far1<em1(IMPC)Wtsi>/Far1<em1(IMPC)Wtsi>	C57BL/6N-Far1<em1(IMPC)Wtsi>	N	37039784
MGI:7524327	M	MP:0014052	increased male germ cell apoptosis	Far1<em1(IMPC)Wtsi>/Far1<em1(IMPC)Wtsi>	C57BL/6N-Far1<em1(IMPC)Wtsi>	N	37039784
MGI:7524327	M	MP:0020550	multinucleated giant male germ cells	Far1<em1(IMPC)Wtsi>/Far1<em1(IMPC)Wtsi>	C57BL/6N-Far1<em1(IMPC)Wtsi>	N	37039784
MGI:7524327	M	MP:0006379	abnormal spermatocyte morphology	Far1<em1(IMPC)Wtsi>/Far1<em1(IMPC)Wtsi>	C57BL/6N-Far1<em1(IMPC)Wtsi>	N	37039784
MGI:7526263	F	MP:0011122	absent primordial ovarian follicles	Elavl2<tm1.2Ysa>/Elavl2<tm1.2Ysa>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	31657143
MGI:7526263	M	MP:0005389	reproductive system phenotype	Elavl2<tm1.2Ysa>/Elavl2<tm1.2Ysa>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	Y	31657143
MGI:7526263	F	MP:0009093	oocyte degeneration	Elavl2<tm1.2Ysa>/Elavl2<tm1.2Ysa>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	31657143
MGI:7526263	F	MP:0001126	abnormal ovary morphology	Elavl2<tm1.2Ysa>/Elavl2<tm1.2Ysa>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	31657143
MGI:7526263	F	MP:0001926	female infertility	Elavl2<tm1.2Ysa>/Elavl2<tm1.2Ysa>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	31657143
MGI:7526263	F	MP:0004805	absent oocytes	Elavl2<tm1.2Ysa>/Elavl2<tm1.2Ysa>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	31657143
MGI:7526263	F	MP:0001127	small ovary	Elavl2<tm1.2Ysa>/Elavl2<tm1.2Ysa>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	N	31657143
MGI:7526270	F	MP:0004805	absent oocytes	Ddx6<em1.1Ysa>/Ddx6<em1.1Ysa>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6NCrlj * CBA/JNCrlj * FVB	N	31657143
MGI:7526270	F	MP:0009361	abnormal primordial ovarian follicle morphology	Ddx6<em1.1Ysa>/Ddx6<em1.1Ysa>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6NCrlj * CBA/JNCrlj * FVB	N	31657143
MGI:7526270	F	MP:0031381	decreased secondary ovarian follicle number	Ddx6<em1.1Ysa>/Ddx6<em1.1Ysa>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6NCrlj * CBA/JNCrlj * FVB	N	31657143
MGI:7526270	F	MP:0011129	decreased tertiary ovarian follicle number	Ddx6<em1.1Ysa>/Ddx6<em1.1Ysa>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6NCrlj * CBA/JNCrlj * FVB	N	31657143
MGI:7526270	F	MP:0011121	decreased primordial ovarian follicle number	Ddx6<em1.1Ysa>/Ddx6<em1.1Ysa>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6NCrlj * CBA/JNCrlj * FVB	N	31657143
MGI:7526270	F	MP:0001131	abnormal ovarian follicle morphology	Ddx6<em1.1Ysa>/Ddx6<em1.1Ysa>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6NCrlj * CBA/JNCrlj * FVB	N	31657143
MGI:7526270	F	MP:0011125	decreased primary ovarian follicle number	Ddx6<em1.1Ysa>/Ddx6<em1.1Ysa>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6NCrlj * CBA/JNCrlj * FVB	N	31657143
MGI:7526270	F	MP:0001926	female infertility	Ddx6<em1.1Ysa>/Ddx6<em1.1Ysa>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6NCrlj * CBA/JNCrlj * FVB	N	31657143
MGI:7526270	F	MP:0001126	abnormal ovary morphology	Ddx6<em1.1Ysa>/Ddx6<em1.1Ysa>,Tg(Ddx4-cre)1Dcas/0	involves: 129S4/SvJaeSor * C57BL/6NCrlj * CBA/JNCrlj * FVB	N	31657143
MGI:7530054	M	MP:0005578	teratozoospermia	Poc1b<em1Xjzha>/Poc1b<em1Xjzha>	C57BL/6J-Poc1b<em1Xjzha>	N	37070736
MGI:7530054	M	MP:0031356	abnormal outer dense fiber morphology	Poc1b<em1Xjzha>/Poc1b<em1Xjzha>	C57BL/6J-Poc1b<em1Xjzha>	N	37070736
MGI:7530054	M	MP:0008892	abnormal sperm flagellum morphology	Poc1b<em1Xjzha>/Poc1b<em1Xjzha>	C57BL/6J-Poc1b<em1Xjzha>	N	37070736
MGI:7530054	M	MP:0006380	abnormal spermatid morphology	Poc1b<em1Xjzha>/Poc1b<em1Xjzha>	C57BL/6J-Poc1b<em1Xjzha>	N	37070736
MGI:7530054	M	MP:0009239	short sperm flagellum	Poc1b<em1Xjzha>/Poc1b<em1Xjzha>	C57BL/6J-Poc1b<em1Xjzha>	N	37070736
MGI:7530054	M	MP:0009831	abnormal sperm midpiece morphology	Poc1b<em1Xjzha>/Poc1b<em1Xjzha>	C57BL/6J-Poc1b<em1Xjzha>	N	37070736
MGI:7530054	M	MP:0001925	male infertility	Poc1b<em1Xjzha>/Poc1b<em1Xjzha>	C57BL/6J-Poc1b<em1Xjzha>	N	37070736
MGI:7530054	M	MP:0008898	abnormal acrosome morphology	Poc1b<em1Xjzha>/Poc1b<em1Xjzha>	C57BL/6J-Poc1b<em1Xjzha>	N	37070736
MGI:7530054	M	MP:0031352	absent sperm axonemal central pair	Poc1b<em1Xjzha>/Poc1b<em1Xjzha>	C57BL/6J-Poc1b<em1Xjzha>	N	37070736
MGI:7530054	M	MP:0002687	oligozoospermia	Poc1b<em1Xjzha>/Poc1b<em1Xjzha>	C57BL/6J-Poc1b<em1Xjzha>	N	37070736
MGI:7530054	M	MP:0020869	immotile sperm	Poc1b<em1Xjzha>/Poc1b<em1Xjzha>	C57BL/6J-Poc1b<em1Xjzha>	N	37070736
MGI:7530054	M	MP:0009230	abnormal sperm head morphology	Poc1b<em1Xjzha>/Poc1b<em1Xjzha>	C57BL/6J-Poc1b<em1Xjzha>	N	37070736
MGI:7530054	M	MP:0009837	abnormal sperm end piece morphology	Poc1b<em1Xjzha>/Poc1b<em1Xjzha>	C57BL/6J-Poc1b<em1Xjzha>	N	37070736
MGI:7531563	M	MP:0020451	decreased sperm progressive motility	Tsnaxip1<em1Osb>/Tsnaxip1<em1Osb>	involves: C57BL/6J * DBA/2J	N	36598146
MGI:7531563	M	MP:0009282	decreased hyperactivated sperm motility	Tsnaxip1<em1Osb>/Tsnaxip1<em1Osb>	involves: C57BL/6J * DBA/2J	N	36598146
MGI:7531563	M	MP:0001922	reduced male fertility	Tsnaxip1<em1Osb>/Tsnaxip1<em1Osb>	involves: C57BL/6J * DBA/2J	N	36598146
MGI:7531571	M	MP:0001922	reduced male fertility	1700010I14Rik<em1Osb>/1700010I14Rik<em1Osb>	involves: C57BL/6J * DBA/2J	N	36598146
MGI:7531571	M	MP:0009282	decreased hyperactivated sperm motility	1700010I14Rik<em1Osb>/1700010I14Rik<em1Osb>	involves: C57BL/6J * DBA/2J	N	36598146
MGI:7531571	M	MP:0020451	decreased sperm progressive motility	1700010I14Rik<em1Osb>/1700010I14Rik<em1Osb>	involves: C57BL/6J * DBA/2J	N	36598146
MGI:7531572	M	MP:0001922	reduced male fertility	1700010I14Rik<em1Osb>/1700010I14Rik<em1Osb>,Tsnaxip1<em1Osb>/Tsnaxip1<em1Osb>	involves: C57BL/6J * DBA/2J	N	36598146
MGI:7531572	M	MP:0009282	decreased hyperactivated sperm motility	1700010I14Rik<em1Osb>/1700010I14Rik<em1Osb>,Tsnaxip1<em1Osb>/Tsnaxip1<em1Osb>	involves: C57BL/6J * DBA/2J	N	36598146
MGI:7531572	M	MP:0020451	decreased sperm progressive motility	1700010I14Rik<em1Osb>/1700010I14Rik<em1Osb>,Tsnaxip1<em1Osb>/Tsnaxip1<em1Osb>	involves: C57BL/6J * DBA/2J	N	36598146
MGI:7538859	M	MP:0001925	male infertility	Tmem249<em1Osb>/Tmem249<em1Osb>	involves: C57BL/6 * DBA/2	N	36993167
MGI:7538859	M	MP:0000242	impaired fertilization	Tmem249<em1Osb>/Tmem249<em1Osb>	involves: C57BL/6 * DBA/2	N	36993167
MGI:7538859	M	MP:0002675	asthenozoospermia	Tmem249<em1Osb>/Tmem249<em1Osb>	involves: C57BL/6 * DBA/2	N	36993167
MGI:7538859	M	MP:0009279	abnormal activated sperm motility	Tmem249<em1Osb>/Tmem249<em1Osb>	involves: C57BL/6 * DBA/2	N	36993167
MGI:7538859	M	MP:0009282	decreased hyperactivated sperm motility	Tmem249<em1Osb>/Tmem249<em1Osb>	involves: C57BL/6 * DBA/2	N	36993167
MGI:7538859	M	MP:0020451	decreased sperm progressive motility	Tmem249<em1Osb>/Tmem249<em1Osb>	involves: C57BL/6 * DBA/2	N	36993167
MGI:7538915	M	MP:0004777	abnormal phospholipid level	Acot12<em1Holi>/Acot12<em1Holi>	involves: C57BL/6J * C57BL/6N	N	37150501
MGI:7538915	M	MP:0003331	increased hepatocellular carcinoma incidence	Acot12<em1Holi>/Acot12<em1Holi>	involves: C57BL/6J * C57BL/6N	N	37150501
MGI:7538915	M	MP:0003333	liver fibrosis	Acot12<em1Holi>/Acot12<em1Holi>	involves: C57BL/6J * C57BL/6N	N	37150501
MGI:7538915	M	MP:0004499	increased incidence of tumors by chemical induction	Acot12<em1Holi>/Acot12<em1Holi>	involves: C57BL/6J * C57BL/6N	N	37150501
MGI:7538915	M	MP:0009355	increased liver triglyceride level	Acot12<em1Holi>/Acot12<em1Holi>	involves: C57BL/6J * C57BL/6N	N	37150501
MGI:7538915	M	MP:0003980	increased circulating phospholipid level	Acot12<em1Holi>/Acot12<em1Holi>	involves: C57BL/6J * C57BL/6N	N	37150501
MGI:7538915	M	MP:0003721	increased tumor growth/size	Acot12<em1Holi>/Acot12<em1Holi>	involves: C57BL/6J * C57BL/6N	N	37150501
MGI:7538915	M	MP:0010027	increased liver cholesterol level	Acot12<em1Holi>/Acot12<em1Holi>	involves: C57BL/6J * C57BL/6N	N	37150501
MGI:7538915	M	MP:0001765	abnormal ion homeostasis	Acot12<em1Holi>/Acot12<em1Holi>	involves: C57BL/6J * C57BL/6N	N	37150501
MGI:7538915	M	MP:0005178	increased circulating cholesterol level	Acot12<em1Holi>/Acot12<em1Holi>	involves: C57BL/6J * C57BL/6N	N	37150501
MGI:7539049	M	MP:0014142	increased body fat mass	Pgap4<em1Osbir>/Pgap4<em1Osbir>	involves: C57BL/6NSlc	N	35151686
MGI:7539049	F	MP:0013670	increased Ly6C-positive immature NK cell number	Pgap4<em1Osbir>/Pgap4<em1Osbir>	involves: C57BL/6NSlc	N	35151686
MGI:7539049	F	MP:0004658	abnormal ventral tubercle of atlas morphology	Pgap4<em1Osbir>/Pgap4<em1Osbir>	involves: C57BL/6NSlc	N	35151686
MGI:7539049	M	MP:0000150	abnormal rib morphology	Pgap4<em1Osbir>/Pgap4<em1Osbir>	involves: C57BL/6NSlc	N	35151686
MGI:7539049	M	MP:0010099	abnormal thoracic cage shape	Pgap4<em1Osbir>/Pgap4<em1Osbir>	involves: C57BL/6NSlc	N	35151686
MGI:7539049	M	MP:0003048	abnormal cervical vertebrae morphology	Pgap4<em1Osbir>/Pgap4<em1Osbir>	involves: C57BL/6NSlc	N	35151686
MGI:7539049	M	MP:0005458	increased percent body fat/body weight	Pgap4<em1Osbir>/Pgap4<em1Osbir>	involves: C57BL/6NSlc	N	35151686
MGI:7539049	M	MP:0011919	abnormal R wave	Pgap4<em1Osbir>/Pgap4<em1Osbir>	involves: C57BL/6NSlc	N	35151686
MGI:7539049	F	MP:0002764	short tibia	Pgap4<em1Osbir>/Pgap4<em1Osbir>	involves: C57BL/6NSlc	N	35151686
MGI:7539049	M	MP:0003795	abnormal bone structure	Pgap4<em1Osbir>/Pgap4<em1Osbir>	involves: C57BL/6NSlc	N	35151686
MGI:7541209	M	MP:0020451	decreased sperm progressive motility	Bbof1<em1Liwe>/Bbof1<em1Liwe>	C57BL/6J-Bbof1<em1Liwe>	N	37494937
MGI:7541209	M	MP:0001925	male infertility	Bbof1<em1Liwe>/Bbof1<em1Liwe>	C57BL/6J-Bbof1<em1Liwe>	N	37494937
MGI:7541209	M	MP:0013209	abnormal motile cilium physiology	Bbof1<em1Liwe>/Bbof1<em1Liwe>	C57BL/6J-Bbof1<em1Liwe>	N	37494937
MGI:7541209	F	MP:0005389	reproductive system phenotype	Bbof1<em1Liwe>/Bbof1<em1Liwe>	C57BL/6J-Bbof1<em1Liwe>	Y	37494937
MGI:7541209	M	MP:0002675	asthenozoospermia	Bbof1<em1Liwe>/Bbof1<em1Liwe>	C57BL/6J-Bbof1<em1Liwe>	N	37494937
MGI:7541209	M	MP:0009838	abnormal sperm axoneme morphology	Bbof1<em1Liwe>/Bbof1<em1Liwe>	C57BL/6J-Bbof1<em1Liwe>	N	37494937
MGI:7541224	M	MP:0003631	nervous system phenotype	Hnrnph2<em3Jpat>/Y	C57BL/6J-Hnrnph2<em3Jpat>	Y	37463454
MGI:7541224	M	MP:0005386	behavior/neurological phenotype	Hnrnph2<em3Jpat>/Y	C57BL/6J-Hnrnph2<em3Jpat>	Y	37463454
MGI:7541224	M	MP:0006276	abnormal autonomic nervous system physiology	Hnrnph2<em3Jpat>/Y	C57BL/6J-Hnrnph2<em3Jpat>	N	37463454
MGI:7541224	M	MP:0000428	abnormal craniofacial morphology	Hnrnph2<em3Jpat>/Y	C57BL/6J-Hnrnph2<em3Jpat>	N	37463454
MGI:7541224	M	MP:0005378	growth/size/body region phenotype	Hnrnph2<em3Jpat>/Y	C57BL/6J-Hnrnph2<em3Jpat>	Y	37463454
MGI:7541224	M	MP:0010769	abnormal survival	Hnrnph2<em3Jpat>/Y	C57BL/6J-Hnrnph2<em3Jpat>	N	37463454
MGI:7541226	M	MP:0000428	abnormal craniofacial morphology	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0001262	decreased body weight	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0000440	domed cranium	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0008414	abnormal spatial reference memory	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0021112	impaired social recognition	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0002083	premature death	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0002572	abnormal emotion/affect behavior	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0001525	impaired balance	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0008525	decreased cranium height	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0001496	audiogenic seizures	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0001405	impaired coordination	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0000097	short maxilla	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0000445	short snout	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0002066	abnormal motor capabilities/coordination/movement	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0001300	ocular hypertelorism	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0003908	decreased stereotypic behavior	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0001891	hydrocephaly	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0010053	decreased grip strength	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0012307	impaired spatial learning	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0001265	decreased body size	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0011620	abnormal habituation to a new environment	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0001402	decreased locomotor activity	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0002797	increased thigmotaxis	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0014114	abnormal cognition	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541226	M	MP:0001363	increased anxiety-related response	Hnrnph2<em2Jpat>/Y	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7541228	M	MP:0000440	domed cranium	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0001525	impaired balance	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0010053	decreased grip strength	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0004994	abnormal brain wave pattern	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0001300	ocular hypertelorism	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0001496	audiogenic seizures	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0001891	hydrocephaly	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0001265	decreased body size	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0021090	abnormal dendrite arborization pattern	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0000428	abnormal craniofacial morphology	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0000088	short mandible	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0005537	abnormal cerebral aqueduct morphology	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0001405	impaired coordination	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0008525	decreased cranium height	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0000097	short maxilla	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0002083	premature death	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0011101	prenatal lethality, incomplete penetrance	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0000445	short snout	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0001262	decreased body weight	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541228	M	MP:0001407	short stride length	Hnrnph2<em1Jpat>/Y	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7541255	M	MP:0020451	decreased sperm progressive motility	Ttc6<em1Cya>/Ttc6<em1Cya>	C57BL/6J-Ttc6<em1Cya>	N	37626901
MGI:7541255	M	MP:0008892	abnormal sperm flagellum morphology	Ttc6<em1Cya>/Ttc6<em1Cya>	C57BL/6J-Ttc6<em1Cya>	N	37626901
MGI:7541255	F	MP:0005389	reproductive system phenotype	Ttc6<em1Cya>/Ttc6<em1Cya>	C57BL/6J-Ttc6<em1Cya>	Y	37626901
MGI:7541255	M	MP:0009243	hairpin sperm flagellum	Ttc6<em1Cya>/Ttc6<em1Cya>	C57BL/6J-Ttc6<em1Cya>	N	37626901
MGI:7541255	M	MP:0030978	impaired binding of sperm to zona pellucida	Ttc6<em1Cya>/Ttc6<em1Cya>	C57BL/6J-Ttc6<em1Cya>	N	37626901
MGI:7541255	M	MP:0001922	reduced male fertility	Ttc6<em1Cya>/Ttc6<em1Cya>	C57BL/6J-Ttc6<em1Cya>	N	37626901
MGI:7542919	F	MP:0005389	reproductive system phenotype	Wee2<em1Zuk>/Wee2<em1Zuk>	involves: C57BL/6J * DBA/2J	Y	37527245
MGI:7542920	F	MP:0001923	reduced female fertility	Wee2<em2Zuk>/Wee2<em2Zuk>	involves: C57BL/6J * DBA/2J	N	37527245
MGI:7542920	F	MP:0005389	reproductive system phenotype	Wee2<em2Zuk>/Wee2<em2Zuk>	involves: C57BL/6J * DBA/2J	Y	37527245
MGI:7542920	F	MP:0001935	decreased litter size	Wee2<em2Zuk>/Wee2<em2Zuk>	involves: C57BL/6J * DBA/2J	N	37527245
MGI:7543156	F	MP:0001883	increased mammary adenocarcinoma incidence	Pten<tm1Hwu>/Pten<tm1Hwu>,Tg(Pgc-cre,-secNluc)#Hcz/0	involves: 129S4/SvJae	N	37291517
MGI:7543174	F	MP:0001935	decreased litter size	D6Ertd527e<em1Psv>/D6Ertd527e<em1Psv>	C57BL/6-D6Ertd527e<em1Psv>	N	36482406
MGI:7543174	F	MP:0001923	reduced female fertility	D6Ertd527e<em1Psv>/D6Ertd527e<em1Psv>	C57BL/6-D6Ertd527e<em1Psv>	N	36482406
MGI:7543286	F	MP:0011939	increased food intake	Gm26330<em1Liuq>/Gm26330<em1Liuq>	C57BL/6-Gm26330<em1Liuq>	N	37329887
MGI:7543286	M	MP:0011941	increased fluid intake	Gm26330<em1Liuq>/Gm26330<em1Liuq>	C57BL/6-Gm26330<em1Liuq>	N	37329887
MGI:7543291	F	MP:0001926	female infertility	Eif4e1b<em1Glin>/Eif4e1b<em1Glin>,Tg(Zp3-cre)93Knw/0	C57BL/6J-Eif4e1b<em1Glin> Tg(Zp3-cre)93Knw	N	36755190
MGI:7543291	F	MP:0003718	maternal effect	Eif4e1b<em1Glin>/Eif4e1b<em1Glin>,Tg(Zp3-cre)93Knw/0	C57BL/6J-Eif4e1b<em1Glin> Tg(Zp3-cre)93Knw	N	36755190
MGI:7543291	F	MP:0004832	enlarged ovary	Eif4e1b<em1Glin>/Eif4e1b<em1Glin>,Tg(Zp3-cre)93Knw/0	C57BL/6J-Eif4e1b<em1Glin> Tg(Zp3-cre)93Knw	N	36755190
MGI:7543291	F	MP:0011128	increased tertiary ovarian follicle number	Eif4e1b<em1Glin>/Eif4e1b<em1Glin>,Tg(Zp3-cre)93Knw/0	C57BL/6J-Eif4e1b<em1Glin> Tg(Zp3-cre)93Knw	N	36755190
MGI:7543291	F	MP:0011124	increased primary ovarian follicle number	Eif4e1b<em1Glin>/Eif4e1b<em1Glin>,Tg(Zp3-cre)93Knw/0	C57BL/6J-Eif4e1b<em1Glin> Tg(Zp3-cre)93Knw	N	36755190
MGI:7543291	F	MP:0031383	increased secondary ovarian follicle number	Eif4e1b<em1Glin>/Eif4e1b<em1Glin>,Tg(Zp3-cre)93Knw/0	C57BL/6J-Eif4e1b<em1Glin> Tg(Zp3-cre)93Knw	N	36755190
MGI:7543291	F	MP:0005389	reproductive system phenotype	Eif4e1b<em1Glin>/Eif4e1b<em1Glin>,Tg(Zp3-cre)93Knw/0	C57BL/6J-Eif4e1b<em1Glin> Tg(Zp3-cre)93Knw	Y	36755190
MGI:7543396	M	MP:0009355	increased liver triglyceride level	Iars1<em2Nsas>/Iars1<em2Nsas>	C57BL/6-Iars1<em2Nsas>	N	37108118
MGI:7543396	M	MP:0031116	microvesicular hepatic steatosis	Iars1<em2Nsas>/Iars1<em2Nsas>	C57BL/6-Iars1<em2Nsas>	N	37108118
MGI:7543396	M	MP:0001262	decreased body weight	Iars1<em2Nsas>/Iars1<em2Nsas>	C57BL/6-Iars1<em2Nsas>	N	37108118
MGI:7543396	M	MP:0005370	liver/biliary system phenotype	Iars1<em2Nsas>/Iars1<em2Nsas>	C57BL/6-Iars1<em2Nsas>	Y	37108118
MGI:7543396	M	MP:0005266	abnormal metabolism	Iars1<em2Nsas>/Iars1<em2Nsas>	C57BL/6-Iars1<em2Nsas>	N	37108118
MGI:7543400	M	MP:0002687	oligozoospermia	Arrdc5<em1Oat>/Arrdc5<em1Oat>	involves: 129S6/SvEvTac * C57BL/6J	N	37069147
MGI:7543400	M	MP:0005578	teratozoospermia	Arrdc5<em1Oat>/Arrdc5<em1Oat>	involves: 129S6/SvEvTac * C57BL/6J	N	37069147
MGI:7543400	M	MP:0001932	abnormal spermiogenesis	Arrdc5<em1Oat>/Arrdc5<em1Oat>	involves: 129S6/SvEvTac * C57BL/6J	N	37069147
MGI:7543400	M	MP:0008898	abnormal acrosome morphology	Arrdc5<em1Oat>/Arrdc5<em1Oat>	involves: 129S6/SvEvTac * C57BL/6J	N	37069147
MGI:7543400	M	MP:0003666	impaired sperm capacitation	Arrdc5<em1Oat>/Arrdc5<em1Oat>	involves: 129S6/SvEvTac * C57BL/6J	N	37069147
MGI:7543400	M	MP:0002675	asthenozoospermia	Arrdc5<em1Oat>/Arrdc5<em1Oat>	involves: 129S6/SvEvTac * C57BL/6J	N	37069147
MGI:7543400	M	MP:0001925	male infertility	Arrdc5<em1Oat>/Arrdc5<em1Oat>	involves: 129S6/SvEvTac * C57BL/6J	N	37069147
MGI:7543400	M	MP:0004542	impaired acrosome reaction	Arrdc5<em1Oat>/Arrdc5<em1Oat>	involves: 129S6/SvEvTac * C57BL/6J	N	37069147
MGI:7543400	F	MP:0005389	reproductive system phenotype	Arrdc5<em1Oat>/Arrdc5<em1Oat>	involves: 129S6/SvEvTac * C57BL/6J	Y	37069147
MGI:7543400	M	MP:0030976	impaired sperm penetration of zona pellucida	Arrdc5<em1Oat>/Arrdc5<em1Oat>	involves: 129S6/SvEvTac * C57BL/6J	N	37069147
MGI:7543400	M	MP:0009233	enlarged sperm head	Arrdc5<em1Oat>/Arrdc5<em1Oat>	involves: 129S6/SvEvTac * C57BL/6J	N	37069147
MGI:7544862	M	MP:0005389	reproductive system phenotype	Spata31g1<em1Ctu>/Spata31g1<em1Ctu>	C57BL/6-Spata31g1<em1Ctu>	N	36871790
MGI:7544864	M	MP:0005389	reproductive system phenotype	4933402N03Rik<em1Ctu>/4933402N03Rik<em1Ctu>	C57BL/6-4933402N03Rik<em1Ctu>	Y	36871790
MGI:7545087	F	MP:0000761	thin diaphragm muscle	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7545087	F	MP:0005388	respiratory system phenotype	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	Y	37751738
MGI:7545087	F	MP:0002279	abnormal diaphragm morphology	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7545087	F	MP:0011086	postnatal lethality, incomplete penetrance	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7545087	F	MP:0003385	abnormal body wall morphology	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7545087	F	MP:0000062	increased bone mineral density	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7545087	F	MP:0012251	abnormal diaphragm development	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7545087	F	MP:0000757	herniated abdominal wall	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7545087	F	MP:0013857	abnormal abdominal muscle morphology	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7545087	F	MP:0010770	preweaning lethality	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7545087	F	MP:0003924	diaphragmatic hernia	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7545087	F	MP:0005376	homeostasis/metabolism phenotype	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	Y	37751738
MGI:7545087	F	MP:0003257	abnormal abdominal wall morphology	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7545087	F	MP:0011088	neonatal lethality, incomplete penetrance	Pls3<em1Bult>/Pls3<em1Bult>	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7545089	F	MP:0000063	decreased bone mineral density	Pls3<em2Bult>/Pls3<em2Bult>	C57BL/6J-Pls3<em2Bult>/BultJ	N	37751738
MGI:7545546	M	MP:0001925	male infertility	Lepr<db-Nokl>/Lepr<db-Nokl>	C57BL/6N-Lepr<db-Nokl>	N	34390703
MGI:7545546	F	MP:0011014	decreased core body temperature	Lepr<db-Nokl>/Lepr<db-Nokl>	C57BL/6N-Lepr<db-Nokl>	N	34390703
MGI:7545546	F	MP:0013279	increased fasting circulating glucose level	Lepr<db-Nokl>/Lepr<db-Nokl>	C57BL/6N-Lepr<db-Nokl>	N	34390703
MGI:7545546	F	MP:0030968	decreased circulating adiponectin level	Lepr<db-Nokl>/Lepr<db-Nokl>	C57BL/6N-Lepr<db-Nokl>	N	34390703
MGI:7545550	F	MP:0011014	decreased core body temperature	Lepr<db>/Lepr<db>	B6NTac.BKS(D)-Lepr<db>	N	34390703
MGI:7545550	F	MP:0013279	increased fasting circulating glucose level	Lepr<db>/Lepr<db>	B6NTac.BKS(D)-Lepr<db>	N	34390703
MGI:7545554	F	MP:0030968	decreased circulating adiponectin level	Lepr<db>/Lepr<db-Nokl>	B6NTac.Cg-Lepr<db> Lepr<db-Nokl>	N	34390703
MGI:7545554	F	MP:0013279	increased fasting circulating glucose level	Lepr<db>/Lepr<db-Nokl>	B6NTac.Cg-Lepr<db> Lepr<db-Nokl>	N	34390703
MGI:7545554	F	MP:0011014	decreased core body temperature	Lepr<db>/Lepr<db-Nokl>	B6NTac.Cg-Lepr<db> Lepr<db-Nokl>	N	34390703
MGI:7545596	M	MP:0004542	impaired acrosome reaction	Glipr1l1<em1Mkob>/Glipr1l1<em1Mkob>	Not Specified	N	31672133
MGI:7545596	M	MP:0031009	abnormal sperm-egg fusion	Glipr1l1<em1Mkob>/Glipr1l1<em1Mkob>	Not Specified	N	31672133
MGI:7546836	M	MP:0009831	abnormal sperm midpiece morphology	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0008892	abnormal sperm flagellum morphology	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0009231	detached acrosome	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0031354	abnormal acrosome assembly	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0001925	male infertility	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0020869	immotile sperm	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0001932	abnormal spermiogenesis	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0009838	abnormal sperm axoneme morphology	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0001156	abnormal spermatogenesis	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0001147	small testis	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0009230	abnormal sperm head morphology	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0002686	globozoospermia	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0009232	abnormal sperm nucleus morphology	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0001153	small seminiferous tubules	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546836	M	MP:0008839	absent acrosome	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546844	M	MP:0008892	abnormal sperm flagellum morphology	Pdcl2<em1Ncvc>/Pdcl2<em1Ncvc>,Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0	involves: C57BL/6 * DBA/2	N	36278277
MGI:7546966	M	MP:0008261	arrest of male meiosis	Fignl1<tm1Osb>/Fignl1<tm1.1Osb>,Tg(Stra8-cre)1Osb/0	involves: C57BL/6	N	37891173
MGI:7546966	M	MP:0002687	oligozoospermia	Fignl1<tm1Osb>/Fignl1<tm1.1Osb>,Tg(Stra8-cre)1Osb/0	involves: C57BL/6	N	37891173
MGI:7546966	M	MP:0009451	abnormal chromosomal synapsis	Fignl1<tm1Osb>/Fignl1<tm1.1Osb>,Tg(Stra8-cre)1Osb/0	involves: C57BL/6	N	37891173
MGI:7546968	M	MP:0008261	arrest of male meiosis	Fignl1<tm1Osb>/Fignl1<tm1.1Osb>,Spo11<tm1Mjn>/Spo11<tm1Mjn>,Tg(Stra8-cre)1Osb/0	involves: 129X1/SvJ * C57BL/6	N	37891173
MGI:7546969	M	MP:0005169	abnormal male meiosis	Fignl1<tm1Osb>/Fignl1<tm1.1Osb>,Swsap1<tm1.1Osb>/Swsap1<tm1.1Osb>,Tg(Stra8-cre)1Osb/0	involves: C57BL/6	N	37891173
MGI:7547102	M	MP:0004000	impaired passive avoidance behavior	Nps<tm1.1Rkr>/Nps<tm1.1Rkr>	involves: 129P2/OlaHsd * C57BL/6J	N	28548278
MGI:7547102	M	MP:0001363	increased anxiety-related response	Nps<tm1.1Rkr>/Nps<tm1.1Rkr>	involves: 129P2/OlaHsd * C57BL/6J	N	28548278
MGI:7547102	M	MP:0001417	decreased exploration in new environment	Nps<tm1.1Rkr>/Nps<tm1.1Rkr>	involves: 129P2/OlaHsd * C57BL/6J	N	28548278
MGI:7547105	F	MP:0001552	increased circulating triglyceride level	Lyplal1<em1Espel>/Lyplal1<em1Espel>	C57BL/6J-Lyplal1<em1Espel>	N	36748836
MGI:7547105	F	MP:0005659	decreased susceptibility to diet-induced obesity	Lyplal1<em1Espel>/Lyplal1<em1Espel>	C57BL/6J-Lyplal1<em1Espel>	N	36748836
MGI:7547105	F	MP:0002942	decreased circulating alanine transaminase level	Lyplal1<em1Espel>/Lyplal1<em1Espel>	C57BL/6J-Lyplal1<em1Espel>	N	36748836
MGI:7547105	F	MP:0001783	decreased white adipose tissue amount	Lyplal1<em1Espel>/Lyplal1<em1Espel>	C57BL/6J-Lyplal1<em1Espel>	N	36748836
MGI:7547105	F	MP:0005376	homeostasis/metabolism phenotype	Lyplal1<em1Espel>/Lyplal1<em1Espel>	C57BL/6J-Lyplal1<em1Espel>	Y	36748836
MGI:7547105	F	MP:0009133	decreased white fat cell size	Lyplal1<em1Espel>/Lyplal1<em1Espel>	C57BL/6J-Lyplal1<em1Espel>	N	36748836
MGI:7547105	F	MP:0002078	abnormal glucose homeostasis	Lyplal1<em1Espel>/Lyplal1<em1Espel>	C57BL/6J-Lyplal1<em1Espel>	N	36748836
MGI:7547105	F	MP:0005632	decreased circulating aspartate transaminase level	Lyplal1<em1Espel>/Lyplal1<em1Espel>	C57BL/6J-Lyplal1<em1Espel>	N	36748836
MGI:7547106	M	MP:0001417	decreased exploration in new environment	Nps<tm1.1Rkr>/Nps<+>	involves: 129P2/OlaHsd * C57BL/6J	N	28548278
MGI:7547388	M	MP:0009456	impaired cued conditioning behavior	Rab39b<tm1Pdad>/Y	B6N.Cg-Rab39b<tm1Pdad>	N	34761259
MGI:7547388	M	MP:0008428	abnormal spatial working memory	Rab39b<tm1Pdad>/Y	B6N.Cg-Rab39b<tm1Pdad>	N	34761259
MGI:7547388	M	MP:0020507	increased dendritic spine density	Rab39b<tm1Pdad>/Y	B6N.Cg-Rab39b<tm1Pdad>	N	34761259
MGI:7547388	M	MP:0009936	abnormal dendritic spine morphology	Rab39b<tm1Pdad>/Y	B6N.Cg-Rab39b<tm1Pdad>	N	34761259
MGI:7547388	M	MP:0021111	decreased social investigation	Rab39b<tm1Pdad>/Y	B6N.Cg-Rab39b<tm1Pdad>	N	34761259
MGI:7547513	M	MP:0008432	abnormal long-term spatial reference memory	Slitrk2<tm1.1Jwum>/Y,Tg(Nes-cre)1Atp/0	involves: C57BL/6J * FVB/N	N	35840571
MGI:7547513	M	MP:0001262	decreased body weight	Slitrk2<tm1.1Jwum>/Y,Tg(Nes-cre)1Atp/0	involves: C57BL/6J * FVB/N	N	35840571
MGI:7547513	M	MP:0004753	abnormal miniature excitatory postsynaptic currents	Slitrk2<tm1.1Jwum>/Y,Tg(Nes-cre)1Atp/0	involves: C57BL/6J * FVB/N	N	35840571
MGI:7547513	M	MP:0001406	abnormal gait	Slitrk2<tm1.1Jwum>/Y,Tg(Nes-cre)1Atp/0	involves: C57BL/6J * FVB/N	N	35840571
MGI:7547513	M	MP:0012307	impaired spatial learning	Slitrk2<tm1.1Jwum>/Y,Tg(Nes-cre)1Atp/0	involves: C57BL/6J * FVB/N	N	35840571
MGI:7547513	M	MP:0020357	abnormal excitatory synapse morphology	Slitrk2<tm1.1Jwum>/Y,Tg(Nes-cre)1Atp/0	involves: C57BL/6J * FVB/N	N	35840571
MGI:7547513	M	MP:0020551	abnormal postsynaptic density morphology	Slitrk2<tm1.1Jwum>/Y,Tg(Nes-cre)1Atp/0	involves: C57BL/6J * FVB/N	N	35840571
MGI:7547513	M	MP:0001364	decreased anxiety-related response	Slitrk2<tm1.1Jwum>/Y,Tg(Nes-cre)1Atp/0	involves: C57BL/6J * FVB/N	N	35840571
MGI:7547523	M	MP:0008414	abnormal spatial reference memory	Slitrk2<tm1.1Jwum>/Y	involves: C57BL/6J	N	35840571
MGI:7547523	M	MP:0020551	abnormal postsynaptic density morphology	Slitrk2<tm1.1Jwum>/Y	involves: C57BL/6J	N	35840571
MGI:7547523	M	MP:0004753	abnormal miniature excitatory postsynaptic currents	Slitrk2<tm1.1Jwum>/Y	involves: C57BL/6J	N	35840571
MGI:7548513	F	MP:0001926	female infertility	Dip2c<em1Ywz>/Dip2c<em1Ywz>	involves: C57BL/6J * DBA/2J	N	32707302
MGI:7548877	F	MP:0008871	abnormal ovarian follicle number	Faap100<em1Jzc>/Faap100<em1Jzc>	involves: C57BL/6J * ICR	N	37580696
MGI:7548877	F	MP:0001750	increased circulating follicle stimulating hormone level	Faap100<em1Jzc>/Faap100<em1Jzc>	involves: C57BL/6J * ICR	N	37580696
MGI:7548877	M	MP:0004852	decreased testis weight	Faap100<em1Jzc>/Faap100<em1Jzc>	involves: C57BL/6J * ICR	N	37580696
MGI:7548877	F	MP:0004833	ovary atrophy	Faap100<em1Jzc>/Faap100<em1Jzc>	involves: C57BL/6J * ICR	N	37580696
MGI:7548877	M	MP:0001147	small testis	Faap100<em1Jzc>/Faap100<em1Jzc>	involves: C57BL/6J * ICR	N	37580696
MGI:7548877	F	MP:0001127	small ovary	Faap100<em1Jzc>/Faap100<em1Jzc>	involves: C57BL/6J * ICR	N	37580696
MGI:7548877	F	MP:0002777	absent ovarian follicles	Faap100<em1Jzc>/Faap100<em1Jzc>	involves: C57BL/6J * ICR	N	37580696
MGI:7548877	F	MP:0004856	decreased ovary weight	Faap100<em1Jzc>/Faap100<em1Jzc>	involves: C57BL/6J * ICR	N	37580696
MGI:7548877	F	MP:0009009	absent estrous cycle	Faap100<em1Jzc>/Faap100<em1Jzc>	involves: C57BL/6J * ICR	N	37580696
MGI:7548877	M	MP:0005159	azoospermia	Faap100<em1Jzc>/Faap100<em1Jzc>	involves: C57BL/6J * ICR	N	37580696
MGI:7549078	F	MP:0008028	pregnancy-related premature death	Rps12<em1.1Nbakr>/Rps12<+>	involves: C57BL/6J * FVB/N	N	37272618
MGI:7551030	F	MP:0010124	decreased bone mineral content	Abcc10<em1(IMPC)Bay>/Abcc10<em1(IMPC)Bay>	C57BL/6N-Abcc10<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551030	F	MP:0000063	decreased bone mineral density	Abcc10<em1(IMPC)Bay>/Abcc10<em1(IMPC)Bay>	C57BL/6N-Abcc10<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551032	M	MP:0005576	decreased pulmonary ventilation	Adipoq<tm1b(KOMP)Wtsi>/Adipoq<tm1b(KOMP)Wtsi>	C57BL/6NCrl-Adipoq<tm1b(KOMP)Wtsi>/Tcp	N	MGI:5576271
MGI:7551037	F	MP:0002792	abnormal retina vasculature morphology	Amt<em1(IMPC)Tcp>/Amt<+>	C57BL/6NCrl-Amt<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551037	M	MP:0003131	increased erythrocyte cell number	Amt<em1(IMPC)Tcp>/Amt<+>	C57BL/6NCrl-Amt<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551037	F	MP:0010097	abnormal retina blood vessel morphology	Amt<em1(IMPC)Tcp>/Amt<+>	C57BL/6NCrl-Amt<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551037	M	MP:0002764	short tibia	Amt<em1(IMPC)Tcp>/Amt<+>	C57BL/6NCrl-Amt<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551038	F	MP:0004258	abnormal placenta size	Amt<em1(IMPC)Tcp>/Amt<em1(IMPC)Tcp>	C57BL/6NCrl-Amt<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551038	F	MP:0003054	spina bifida	Amt<em1(IMPC)Tcp>/Amt<em1(IMPC)Tcp>	C57BL/6NCrl-Amt<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551039	F	MP:0005011	increased eosinophil cell number	Ang<tm1.1(KOMP)Vlcg>/Ang<tm1.1(KOMP)Vlcg>	C57BL/6N-Ang<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7551042	F	MP:0005278	abnormal cholesterol homeostasis	Ano4<em1(IMPC)Kmpc>/Ano4<em1(IMPC)Kmpc>	C57BL/6NTac-Ano4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551042	F	MP:0001399	hyperactivity	Ano4<em1(IMPC)Kmpc>/Ano4<em1(IMPC)Kmpc>	C57BL/6NTac-Ano4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551042	F	MP:0010124	decreased bone mineral content	Ano4<em1(IMPC)Kmpc>/Ano4<em1(IMPC)Kmpc>	C57BL/6NTac-Ano4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551043	F	MP:0010124	decreased bone mineral content	Ap1g2<em1(IMPC)Bay>/Ap1g2<em1(IMPC)Bay>	C57BL/6N-Ap1g2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551043	F	MP:0000063	decreased bone mineral density	Ap1g2<em1(IMPC)Bay>/Ap1g2<em1(IMPC)Bay>	C57BL/6N-Ap1g2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551045	F	MP:0005632	decreased circulating aspartate transaminase level	Arl14<em1(IMPC)J>/Arl14<em1(IMPC)J>	C57BL/6NJ-Arl14<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551047	M	MP:0001925	male infertility	Atp10a<em1(IMPC)Tcp>/Atp10a<em1(IMPC)Tcp>	C57BL/6NCrl-Atp10a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551047	M	MP:0001415	increased exploration in new environment	Atp10a<em1(IMPC)Tcp>/Atp10a<em1(IMPC)Tcp>	C57BL/6NCrl-Atp10a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551047	F	MP:0001126	abnormal ovary morphology	Atp10a<em1(IMPC)Tcp>/Atp10a<em1(IMPC)Tcp>	C57BL/6NCrl-Atp10a<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551051	F	MP:0001392	abnormal locomotor behavior	Bcl9<em1(IMPC)Bay>/Bcl9<+>	C57BL/6N-Bcl9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551051	M	MP:0001697	abnormal embryo size	Bcl9<em1(IMPC)Bay>/Bcl9<+>	C57BL/6N-Bcl9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551051	F	MP:0001399	hyperactivity	Bcl9<em1(IMPC)Bay>/Bcl9<+>	C57BL/6N-Bcl9<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551052	F	MP:0000220	increased monocyte cell number	Bloc1s4<em1(IMPC)Mbp>/Bloc1s4<em1(IMPC)Mbp>	C57BL/6NCrl-Bloc1s4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551052	F	MP:0005567	decreased circulating total protein level	Bloc1s4<em1(IMPC)Mbp>/Bloc1s4<em1(IMPC)Mbp>	C57BL/6NCrl-Bloc1s4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551053	M	MP:0002059	abnormal seminal vesicle morphology	Bloc1s5<em1(IMPC)Tcp>/Bloc1s5<em1(IMPC)Tcp>	C57BL/6NCrl-Bloc1s5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551053	M	MP:0002060	abnormal skin morphology	Bloc1s5<em1(IMPC)Tcp>/Bloc1s5<em1(IMPC)Tcp>	C57BL/6NCrl-Bloc1s5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551053	F	MP:0010097	abnormal retina blood vessel morphology	Bloc1s5<em1(IMPC)Tcp>/Bloc1s5<em1(IMPC)Tcp>	C57BL/6NCrl-Bloc1s5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551053	F	MP:0001325	abnormal retina morphology	Bloc1s5<em1(IMPC)Tcp>/Bloc1s5<em1(IMPC)Tcp>	C57BL/6NCrl-Bloc1s5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551054	F	MP:0005011	increased eosinophil cell number	Brix1<tm1b(KOMP)Mbp>/Brix1<+>	C57BL/6N-Brix1<tm1b(KOMP)Mbp>/Mhzh	N	MGI:5576271
MGI:7551054	F	MP:0002606	increased basophil cell number	Brix1<tm1b(KOMP)Mbp>/Brix1<+>	C57BL/6N-Brix1<tm1b(KOMP)Mbp>/Mhzh	N	MGI:5576271
MGI:7551054	M	MP:0001488	increased startle reflex	Brix1<tm1b(KOMP)Mbp>/Brix1<+>	C57BL/6N-Brix1<tm1b(KOMP)Mbp>/Mhzh	N	MGI:5576271
MGI:7551055	M	MP:0004952	increased spleen weight	C9orf72<tm1.1(KOMP)Mbp>/C9orf72<tm1.1(KOMP)Mbp>	C57BL/6N-C9orf72<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551055	M	MP:0010025	decreased total body fat amount	C9orf72<tm1.1(KOMP)Mbp>/C9orf72<tm1.1(KOMP)Mbp>	C57BL/6N-C9orf72<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551055	M	MP:0001147	small testis	C9orf72<tm1.1(KOMP)Mbp>/C9orf72<tm1.1(KOMP)Mbp>	C57BL/6N-C9orf72<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551055	M	MP:0000702	enlarged lymph nodes	C9orf72<tm1.1(KOMP)Mbp>/C9orf72<tm1.1(KOMP)Mbp>	C57BL/6N-C9orf72<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551055	M	MP:0003960	increased lean body mass	C9orf72<tm1.1(KOMP)Mbp>/C9orf72<tm1.1(KOMP)Mbp>	C57BL/6N-C9orf72<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551056	M	MP:0011964	increased total retina thickness	Cacng7<em1(IMPC)Bay>/Cacng7<em1(IMPC)Bay>	C57BL/6N-Cacng7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551056	F	MP:0010053	decreased grip strength	Cacng7<em1(IMPC)Bay>/Cacng7<em1(IMPC)Bay>	C57BL/6N-Cacng7<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551057	F	MP:0002792	abnormal retina vasculature morphology	Calhm4<em1(IMPC)Tcp>/Calhm4<em1(IMPC)Tcp>	C57BL/6NCrl-Calhm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551057	M	MP:0009142	decreased prepulse inhibition	Calhm4<em1(IMPC)Tcp>/Calhm4<em1(IMPC)Tcp>	C57BL/6NCrl-Calhm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551057	F	MP:0010097	abnormal retina blood vessel morphology	Calhm4<em1(IMPC)Tcp>/Calhm4<em1(IMPC)Tcp>	C57BL/6NCrl-Calhm4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551060	M	MP:0001925	male infertility	Catsper2<em1(IMPC)Mbp>/Catsper2<em1(IMPC)Mbp>	C57BL/6NCrl-Catsper2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551061	F	MP:0005561	increased mean corpuscular hemoglobin	Cavin3<tm1.1(KOMP)Vlcg>/Cavin3<tm1.1(KOMP)Vlcg>	C57BL/6N-Cavin3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7551061	F	MP:0010067	increased red blood cell distribution width	Cavin3<tm1.1(KOMP)Vlcg>/Cavin3<tm1.1(KOMP)Vlcg>	C57BL/6N-Cavin3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7551061	F	MP:0002599	increased mean platelet volume	Cavin3<tm1.1(KOMP)Vlcg>/Cavin3<tm1.1(KOMP)Vlcg>	C57BL/6N-Cavin3<tm1.1(KOMP)Vlcg>/Ucd	N	MGI:5576271
MGI:7551062	M	MP:0000274	enlarged heart	Ccdc110<em1(IMPC)Ccpcz>/Ccdc110<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccdc110<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551062	M	MP:0001146	abnormal testis morphology	Ccdc110<em1(IMPC)Ccpcz>/Ccdc110<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccdc110<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551062	M	MP:0000689	abnormal spleen morphology	Ccdc110<em1(IMPC)Ccpcz>/Ccdc110<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccdc110<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551062	M	MP:0000266	abnormal heart morphology	Ccdc110<em1(IMPC)Ccpcz>/Ccdc110<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccdc110<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551062	M	MP:0000691	enlarged spleen	Ccdc110<em1(IMPC)Ccpcz>/Ccdc110<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ccdc110<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551063	M	MP:0001146	abnormal testis morphology	Ccdc88c<tm1.1(KOMP)Mbp>/Ccdc88c<tm1.1(KOMP)Mbp>	C57BL/6N-Ccdc88c<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551063	M	MP:0001147	small testis	Ccdc88c<tm1.1(KOMP)Mbp>/Ccdc88c<tm1.1(KOMP)Mbp>	C57BL/6N-Ccdc88c<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551066	M	MP:0011110	preweaning lethality, incomplete penetrance	Cd68<em1(IMPC)Bay>/Cd68<em1(IMPC)Bay>	C57BL/6N-Cd68<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551071	M	MP:0001925	male infertility	Cep295<em1(IMPC)Bay>/Cep295<em1(IMPC)Bay>	C57BL/6N-Cep295<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551071	F	MP:0001697	abnormal embryo size	Cep295<em1(IMPC)Bay>/Cep295<em1(IMPC)Bay>	C57BL/6N-Cep295<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551072	M	MP:0002599	increased mean platelet volume	Chrac1<tm1.1(KOMP)Vlcg>/Chrac1<tm1.1(KOMP)Vlcg>	C57BL/6N-Chrac1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7551072	M	MP:0003179	thrombocytopenia	Chrac1<tm1.1(KOMP)Vlcg>/Chrac1<tm1.1(KOMP)Vlcg>	C57BL/6N-Chrac1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7551074	F	MP:0002060	abnormal skin morphology	Cib4<em1(IMPC)Mbp>/Cib4<em1(IMPC)Mbp>	C57BL/6NCrl-Cib4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551074	M	MP:0001925	male infertility	Cib4<em1(IMPC)Mbp>/Cib4<em1(IMPC)Mbp>	C57BL/6NCrl-Cib4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551074	M	MP:0002092	abnormal eye morphology	Cib4<em1(IMPC)Mbp>/Cib4<em1(IMPC)Mbp>	C57BL/6NCrl-Cib4<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551075	M	MP:0002092	abnormal eye morphology	Clcn1<em1(IMPC)Mbp>/Clcn1<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551075	M	MP:0001489	decreased startle reflex	Clcn1<em1(IMPC)Mbp>/Clcn1<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551075	M	MP:0002965	increased circulating serum albumin level	Clcn1<em1(IMPC)Mbp>/Clcn1<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551075	F	MP:0001926	female infertility	Clcn1<em1(IMPC)Mbp>/Clcn1<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551075	M	MP:0001925	male infertility	Clcn1<em1(IMPC)Mbp>/Clcn1<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551075	M	MP:0001297	microphthalmia	Clcn1<em1(IMPC)Mbp>/Clcn1<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551075	M	MP:0005560	decreased circulating glucose level	Clcn1<em1(IMPC)Mbp>/Clcn1<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551075	M	MP:0004924	abnormal behavior	Clcn1<em1(IMPC)Mbp>/Clcn1<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551075	M	MP:0020870	decreased thigmotaxis	Clcn1<em1(IMPC)Mbp>/Clcn1<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551075	M	MP:0000223	decreased monocyte cell number	Clcn1<em1(IMPC)Mbp>/Clcn1<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551075	F	MP:0005278	abnormal cholesterol homeostasis	Clcn1<em1(IMPC)Mbp>/Clcn1<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551075	F	MP:0001417	decreased exploration in new environment	Clcn1<em1(IMPC)Mbp>/Clcn1<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551075	M	MP:0000186	decreased circulating HDL cholesterol level	Clcn1<em1(IMPC)Mbp>/Clcn1<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551076	F	MP:0002092	abnormal eye morphology	Clcn6<em1(IMPC)Mbp>/Clcn6<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551076	F	MP:0001297	microphthalmia	Clcn6<em1(IMPC)Mbp>/Clcn6<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551076	M	MP:0020421	increased freezing behavior	Clcn6<em1(IMPC)Mbp>/Clcn6<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551076	F	MP:0001402	decreased locomotor activity	Clcn6<em1(IMPC)Mbp>/Clcn6<em1(IMPC)Mbp>	C57BL/6NCrl-Clcn6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551077	F	MP:0001120	abnormal uterus morphology	Clic6<em1(IMPC)Mbp>/Clic6<em1(IMPC)Mbp>	C57BL/6NCrl-Clic6<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551079	F	MP:0010097	abnormal retina blood vessel morphology	Col28a1<em1(IMPC)Tcp>/Col28a1<em1(IMPC)Tcp>	C57BL/6NCrl-Col28a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551079	F	MP:0002792	abnormal retina vasculature morphology	Col28a1<em1(IMPC)Tcp>/Col28a1<em1(IMPC)Tcp>	C57BL/6NCrl-Col28a1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551080	F	MP:0000182	increased circulating LDL cholesterol level	Col6a3<em1(IMPC)Kmpc>/Col6a3<em1(IMPC)Kmpc>	C57BL/6NTac-Col6a3<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551080	F	MP:0005278	abnormal cholesterol homeostasis	Col6a3<em1(IMPC)Kmpc>/Col6a3<em1(IMPC)Kmpc>	C57BL/6NTac-Col6a3<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551082	M	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Cpm<em1(IMPC)Ccpcz>/Cpm<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cpm<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551082	M	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number	Cpm<em1(IMPC)Ccpcz>/Cpm<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cpm<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551082	M	MP:0005387	immune system phenotype	Cpm<em1(IMPC)Ccpcz>/Cpm<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cpm<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551082	M	MP:0013772	increased effector memory T-helper cell number	Cpm<em1(IMPC)Ccpcz>/Cpm<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cpm<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551082	M	MP:0001262	decreased body weight	Cpm<em1(IMPC)Ccpcz>/Cpm<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cpm<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551083	M	MP:0001417	decreased exploration in new environment	Crocc<em1(IMPC)Bay>/Crocc<em1(IMPC)Bay>	C57BL/6N-Crocc<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551084	M	MP:0011964	increased total retina thickness	Crybb1<em1(IMPC)Bay>/Crybb1<em1(IMPC)Bay>	C57BL/6N-Crybb1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551086	F	MP:0004924	abnormal behavior	Dapl1<em1(IMPC)Kmpc>/Dapl1<em1(IMPC)Kmpc>	C57BL/6NTac-Dapl1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551086	M	MP:0002075	abnormal coat/hair pigmentation	Dapl1<em1(IMPC)Kmpc>/Dapl1<em1(IMPC)Kmpc>	C57BL/6NTac-Dapl1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551086	F	MP:0020870	decreased thigmotaxis	Dapl1<em1(IMPC)Kmpc>/Dapl1<em1(IMPC)Kmpc>	C57BL/6NTac-Dapl1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551086	M	MP:0001417	decreased exploration in new environment	Dapl1<em1(IMPC)Kmpc>/Dapl1<em1(IMPC)Kmpc>	C57BL/6NTac-Dapl1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551086	F	MP:0002834	decreased heart weight	Dapl1<em1(IMPC)Kmpc>/Dapl1<em1(IMPC)Kmpc>	C57BL/6NTac-Dapl1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551086	F	MP:0000063	decreased bone mineral density	Dapl1<em1(IMPC)Kmpc>/Dapl1<em1(IMPC)Kmpc>	C57BL/6NTac-Dapl1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551087	F	MP:0000154	rib fusion	Dcaf15<tm1a(EUCOMM)Hmgu>/Dcaf15<tm1a(EUCOMM)Hmgu>	C57BL/6NCrl-Dcaf15<tm1a(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:7551087	F	MP:0000455	abnormal maxilla morphology	Dcaf15<tm1a(EUCOMM)Hmgu>/Dcaf15<tm1a(EUCOMM)Hmgu>	C57BL/6NCrl-Dcaf15<tm1a(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:7551087	F	MP:0004599	abnormal vertebral arch morphology	Dcaf15<tm1a(EUCOMM)Hmgu>/Dcaf15<tm1a(EUCOMM)Hmgu>	C57BL/6NCrl-Dcaf15<tm1a(EUCOMM)Hmgu>/Ccpcz	N	MGI:5576271
MGI:7551088	M	MP:0002100	abnormal tooth morphology	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	M	MP:0001325	abnormal retina morphology	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	M	MP:0001262	decreased body weight	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	F	MP:0011044	increased lung elastance	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	M	MP:0002339	abnormal lymph node morphology	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	M	MP:0000274	enlarged heart	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	M	MP:0008044	increased NK cell number	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	F	MP:0004952	increased spleen weight	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	M	MP:0001399	hyperactivity	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	F	MP:0000691	enlarged spleen	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	M	MP:0000702	enlarged lymph nodes	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	F	MP:0001402	decreased locomotor activity	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	F	MP:0000689	abnormal spleen morphology	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	F	MP:0000692	small spleen	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551088	M	MP:0000266	abnormal heart morphology	Dcaf5<em1(IMPC)Ccpcz>/Dcaf5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Dcaf5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551089	M	MP:0001284	absent vibrissae	Dclk3<em1(IMPC)J>/Dclk3<em1(IMPC)J>	C57BL/6NJ-Dclk3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551091	F	MP:0001364	decreased anxiety-related response	Defb1<em1(IMPC)Mbp>/Defb1<em1(IMPC)Mbp>	C57BL/6NCrl-Defb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551091	F	MP:0020870	decreased thigmotaxis	Defb1<em1(IMPC)Mbp>/Defb1<em1(IMPC)Mbp>	C57BL/6NCrl-Defb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551091	F	MP:0004924	abnormal behavior	Defb1<em1(IMPC)Mbp>/Defb1<em1(IMPC)Mbp>	C57BL/6NCrl-Defb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551091	F	MP:0001402	decreased locomotor activity	Defb1<em1(IMPC)Mbp>/Defb1<em1(IMPC)Mbp>	C57BL/6NCrl-Defb1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551092	F	MP:0002092	abnormal eye morphology	Degs1<em1(IMPC)Mbp>/Degs1<+>	C57BL/6NCrl-Degs1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551098	M	MP:0005505	thrombocytosis	Ehf<em1(IMPC)Kmpc>/Ehf<em1(IMPC)Kmpc>	C57BL/6NTac-Ehf<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551098	M	MP:0000208	decreased hematocrit	Ehf<em1(IMPC)Kmpc>/Ehf<em1(IMPC)Kmpc>	C57BL/6NTac-Ehf<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551098	M	MP:0002874	decreased hemoglobin content	Ehf<em1(IMPC)Kmpc>/Ehf<em1(IMPC)Kmpc>	C57BL/6NTac-Ehf<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551098	F	MP:0001402	decreased locomotor activity	Ehf<em1(IMPC)Kmpc>/Ehf<em1(IMPC)Kmpc>	C57BL/6NTac-Ehf<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551098	M	MP:0005292	improved glucose tolerance	Ehf<em1(IMPC)Kmpc>/Ehf<em1(IMPC)Kmpc>	C57BL/6NTac-Ehf<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551099	M	MP:0000579	abnormal nail morphology	Elavl2<em1(IMPC)J>/Elavl2<+>	C57BL/6NJ-Elavl2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551103	F	MP:0001399	hyperactivity	Etv4<em1(IMPC)Kmpc>/Etv4<em1(IMPC)Kmpc>	C57BL/6NTac-Etv4<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551104	M	MP:0010506	prolonged RR interval	Fam118a<em1(IMPC)J>/Fam118a<em1(IMPC)J>	C57BL/6NJ-Fam118a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551104	M	MP:0005333	decreased heart rate	Fam118a<em1(IMPC)J>/Fam118a<em1(IMPC)J>	C57BL/6NJ-Fam118a<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551105	M	MP:0001925	male infertility	Fam149b<em1(IMPC)Bay>/Fam149b<em1(IMPC)Bay>	C57BL/6N-Fam149b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551108	F	MP:0005344	increased circulating bilirubin level	Fbrs<em1(IMPC)J>/Fbrs<+>	C57BL/6NJ-Fbrs<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551108	M	MP:0002942	decreased circulating alanine transaminase level	Fbrs<em1(IMPC)J>/Fbrs<+>	C57BL/6NJ-Fbrs<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551108	M	MP:0005635	decreased circulating bilirubin level	Fbrs<em1(IMPC)J>/Fbrs<+>	C57BL/6NJ-Fbrs<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551108	F	MP:0005278	abnormal cholesterol homeostasis	Fbrs<em1(IMPC)J>/Fbrs<+>	C57BL/6NJ-Fbrs<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551108	M	MP:0001304	cataract	Fbrs<em1(IMPC)J>/Fbrs<+>	C57BL/6NJ-Fbrs<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551108	M	MP:0005632	decreased circulating aspartate transaminase level	Fbrs<em1(IMPC)J>/Fbrs<+>	C57BL/6NJ-Fbrs<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551108	F	MP:0002966	decreased circulating alkaline phosphatase level	Fbrs<em1(IMPC)J>/Fbrs<+>	C57BL/6NJ-Fbrs<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551112	F	MP:0002981	increased liver weight	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0000219	increased neutrophil cell number	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	M	MP:0002311	abnormal inspiratory capacity	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0004953	decreased spleen weight	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	M	MP:0005599	increased cardiac muscle contractility	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	M	MP:0001944	abnormal pancreas morphology	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0000494	abnormal cecum morphology	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0000709	enlarged thymus	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0000759	abnormal skeletal muscle morphology	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0005505	thrombocytosis	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0001402	decreased locomotor activity	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	M	MP:0005292	improved glucose tolerance	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0010068	decreased red blood cell distribution width	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0002833	increased heart weight	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	M	MP:0001262	decreased body weight	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0008810	increased circulating iron level	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	M	MP:0010574	dilated aorta	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0000703	abnormal thymus morphology	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0009476	enlarged cecum	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0005016	decreased lymphocyte cell number	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	F	MP:0010053	decreased grip strength	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551112	M	MP:0010379	decreased respiratory quotient	Fnip1<em1(IMPC)Ccpcz>/Fnip1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551117	F	MP:0010097	abnormal retina blood vessel morphology	Gmps<em1(IMPC)Tcp>/Gmps<+>	C57BL/6NCrl-Gmps<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551117	M	MP:0000218	increased leukocyte cell number	Gmps<em1(IMPC)Tcp>/Gmps<+>	C57BL/6NCrl-Gmps<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551117	M	MP:0010024	increased total body fat amount	Gmps<em1(IMPC)Tcp>/Gmps<+>	C57BL/6NCrl-Gmps<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551117	F	MP:0002792	abnormal retina vasculature morphology	Gmps<em1(IMPC)Tcp>/Gmps<+>	C57BL/6NCrl-Gmps<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551117	F	MP:0001392	abnormal locomotor behavior	Gmps<em1(IMPC)Tcp>/Gmps<+>	C57BL/6NCrl-Gmps<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551117	M	MP:0003961	decreased lean body mass	Gmps<em1(IMPC)Tcp>/Gmps<+>	C57BL/6NCrl-Gmps<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551117	M	MP:0005013	increased lymphocyte cell number	Gmps<em1(IMPC)Tcp>/Gmps<+>	C57BL/6NCrl-Gmps<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551119	F	MP:0005278	abnormal cholesterol homeostasis	Gna14<em1(IMPC)Kmpc>/Gna14<em1(IMPC)Kmpc>	C57BL/6NTac-Gna14<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551120	F	MP:0010097	abnormal retina blood vessel morphology	Gnb1l<em1(IMPC)Tcp>/Gnb1l<+>	C57BL/6NCrl-Gnb1l<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551120	F	MP:0002792	abnormal retina vasculature morphology	Gnb1l<em1(IMPC)Tcp>/Gnb1l<+>	C57BL/6NCrl-Gnb1l<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551122	M	MP:0010052	increased grip strength	Gng12<em1(IMPC)J>/Gng12<em1(IMPC)J>	C57BL/6NJ-Gng12<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551123	M	MP:0011110	preweaning lethality, incomplete penetrance	Golga4<em1(IMPC)Bay>/Golga4<em1(IMPC)Bay>	C57BL/6N-Golga4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551126	M	MP:0010025	decreased total body fat amount	Gpr55<em1(IMPC)Mbp>/Gpr55<em1(IMPC)Mbp>	C57BL/6NCrl-Gpr55<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551126	M	MP:0003960	increased lean body mass	Gpr55<em1(IMPC)Mbp>/Gpr55<em1(IMPC)Mbp>	C57BL/6NCrl-Gpr55<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551128	F	MP:0001399	hyperactivity	Gulo<em1(IMPC)Ccpcz>/Gulo<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gulo<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551128	M	MP:0003961	decreased lean body mass	Gulo<em1(IMPC)Ccpcz>/Gulo<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gulo<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551128	F	MP:0000689	abnormal spleen morphology	Gulo<em1(IMPC)Ccpcz>/Gulo<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gulo<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551128	F	MP:0000691	enlarged spleen	Gulo<em1(IMPC)Ccpcz>/Gulo<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gulo<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551128	M	MP:0001293	anophthalmia	Gulo<em1(IMPC)Ccpcz>/Gulo<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gulo<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551128	M	MP:0000266	abnormal heart morphology	Gulo<em1(IMPC)Ccpcz>/Gulo<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gulo<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551128	M	MP:0002092	abnormal eye morphology	Gulo<em1(IMPC)Ccpcz>/Gulo<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gulo<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551128	M	MP:0000274	enlarged heart	Gulo<em1(IMPC)Ccpcz>/Gulo<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gulo<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551130	M	MP:0000538	abnormal urinary bladder morphology	H2-Q10<tm1.1(KOMP)Mbp>/H2-Q10<tm1.1(KOMP)Mbp>	C57BL/6NCrl-H2-Q10<tm1.1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551130	M	MP:0011625	cystolithiasis	H2-Q10<tm1.1(KOMP)Mbp>/H2-Q10<tm1.1(KOMP)Mbp>	C57BL/6NCrl-H2-Q10<tm1.1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551132	M	MP:0002176	increased brain weight	Hirip3<tm1.1(KOMP)Mbp>/Hirip3<tm1.1(KOMP)Mbp>	C57BL/6N-Hirip3<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551132	F	MP:0001120	abnormal uterus morphology	Hirip3<tm1.1(KOMP)Mbp>/Hirip3<tm1.1(KOMP)Mbp>	C57BL/6N-Hirip3<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551132	F	MP:0002833	increased heart weight	Hirip3<tm1.1(KOMP)Mbp>/Hirip3<tm1.1(KOMP)Mbp>	C57BL/6N-Hirip3<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551132	F	MP:0002606	increased basophil cell number	Hirip3<tm1.1(KOMP)Mbp>/Hirip3<tm1.1(KOMP)Mbp>	C57BL/6N-Hirip3<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551132	F	MP:0000219	increased neutrophil cell number	Hirip3<tm1.1(KOMP)Mbp>/Hirip3<tm1.1(KOMP)Mbp>	C57BL/6N-Hirip3<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551133	F	MP:0010024	increased total body fat amount	Hkdc1<em1(IMPC)Bay>/Hkdc1<em1(IMPC)Bay>	C57BL/6N-Hkdc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551133	F	MP:0003961	decreased lean body mass	Hkdc1<em1(IMPC)Bay>/Hkdc1<em1(IMPC)Bay>	C57BL/6N-Hkdc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551133	M	MP:0000063	decreased bone mineral density	Hkdc1<em1(IMPC)Bay>/Hkdc1<em1(IMPC)Bay>	C57BL/6N-Hkdc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551134	M	MP:0005635	decreased circulating bilirubin level	Igfbp6<em1(IMPC)J>/Igfbp6<em1(IMPC)J>	C57BL/6NJ-Igfbp6<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551135	F	MP:0000691	enlarged spleen	Il1r1<em1(IMPC)Ccpcz>/Il1r1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Il1r1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551135	M	MP:0002135	abnormal kidney morphology	Il1r1<em1(IMPC)Ccpcz>/Il1r1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Il1r1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551135	M	MP:0000266	abnormal heart morphology	Il1r1<em1(IMPC)Ccpcz>/Il1r1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Il1r1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551135	M	MP:0000274	enlarged heart	Il1r1<em1(IMPC)Ccpcz>/Il1r1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Il1r1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551135	F	MP:0000689	abnormal spleen morphology	Il1r1<em1(IMPC)Ccpcz>/Il1r1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Il1r1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551135	M	MP:0003068	enlarged kidney	Il1r1<em1(IMPC)Ccpcz>/Il1r1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Il1r1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551135	M	MP:0003917	increased kidney weight	Il1r1<em1(IMPC)Ccpcz>/Il1r1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Il1r1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551136	M	MP:0001148	enlarged testis	Il21<tm1.1(KOMP)Mbp>/Il21<tm1.1(KOMP)Mbp>	C57BL/6NCrl-Il21<tm1.1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551137	F	MP:0002092	abnormal eye morphology	Impg2<em1(IMPC)Mbp>/Impg2<em1(IMPC)Mbp>	C57BL/6NCrl-Impg2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551137	M	MP:0002941	increased circulating alanine transaminase level	Impg2<em1(IMPC)Mbp>/Impg2<em1(IMPC)Mbp>	C57BL/6NCrl-Impg2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551139	M	MP:0002626	increased heart rate	Iqgap3<em1(IMPC)Bay>/Iqgap3<+>	C57BL/6N-Iqgap3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551140	M	MP:0000598	abnormal liver morphology	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	M	MP:0003961	decreased lean body mass	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	M	MP:0002059	abnormal seminal vesicle morphology	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	M	MP:0000219	increased neutrophil cell number	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	F	MP:0010067	increased red blood cell distribution width	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	M	MP:0005016	decreased lymphocyte cell number	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	M	MP:0002874	decreased hemoglobin content	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	M	MP:0001157	small seminal vesicle	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	M	MP:0000599	enlarged liver	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	M	MP:0005011	increased eosinophil cell number	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	M	MP:0005561	increased mean corpuscular hemoglobin	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	M	MP:0009476	enlarged cecum	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	M	MP:0002875	decreased erythrocyte cell number	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	M	MP:0000494	abnormal cecum morphology	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551140	M	MP:0013279	increased fasting circulating glucose level	Irag1<em1(IMPC)Ccpcz>/Irag1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Irag1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551142	F	MP:0001325	abnormal retina morphology	Irf2bpl<em2(IMPC)Bay>/Irf2bpl<+>	C57BL/6N-Irf2bpl<em2(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551145	M	MP:0000702	enlarged lymph nodes	Kcnab2<em1(IMPC)Mbp>/Kcnab2<em1(IMPC)Mbp>	C57BL/6NCrl-Kcnab2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551145	F	MP:0003961	decreased lean body mass	Kcnab2<em1(IMPC)Mbp>/Kcnab2<em1(IMPC)Mbp>	C57BL/6NCrl-Kcnab2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551145	F	MP:0002092	abnormal eye morphology	Kcnab2<em1(IMPC)Mbp>/Kcnab2<em1(IMPC)Mbp>	C57BL/6NCrl-Kcnab2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551145	M	MP:0010052	increased grip strength	Kcnab2<em1(IMPC)Mbp>/Kcnab2<em1(IMPC)Mbp>	C57BL/6NCrl-Kcnab2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551145	F	MP:0010024	increased total body fat amount	Kcnab2<em1(IMPC)Mbp>/Kcnab2<em1(IMPC)Mbp>	C57BL/6NCrl-Kcnab2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551145	M	MP:0002339	abnormal lymph node morphology	Kcnab2<em1(IMPC)Mbp>/Kcnab2<em1(IMPC)Mbp>	C57BL/6NCrl-Kcnab2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551145	M	MP:0001399	hyperactivity	Kcnab2<em1(IMPC)Mbp>/Kcnab2<em1(IMPC)Mbp>	C57BL/6NCrl-Kcnab2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551146	M	MP:0002092	abnormal eye morphology	Kcne3<tm1.1(KOMP)Vlcg>/Kcne3<tm1.1(KOMP)Vlcg>	C57BL/6NCrl-Kcne3<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7551146	F	MP:0005567	decreased circulating total protein level	Kcne3<tm1.1(KOMP)Vlcg>/Kcne3<tm1.1(KOMP)Vlcg>	C57BL/6NCrl-Kcne3<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7551147	F	MP:0001303	abnormal lens morphology	Kcng1<em1(IMPC)Tcp>/Kcng1<em1(IMPC)Tcp>	C57BL/6NCrl-Kcng1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551147	F	MP:0001304	cataract	Kcng1<em1(IMPC)Tcp>/Kcng1<em1(IMPC)Tcp>	C57BL/6NCrl-Kcng1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551147	M	MP:0009142	decreased prepulse inhibition	Kcng1<em1(IMPC)Tcp>/Kcng1<em1(IMPC)Tcp>	C57BL/6NCrl-Kcng1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551148	F	MP:0000220	increased monocyte cell number	Kcng3<em1(IMPC)Mbp>/Kcng3<em1(IMPC)Mbp>	C57BL/6NCrl-Kcng3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551150	F	MP:0001402	decreased locomotor activity	Krtap9-3<em1(IMPC)Bay>/Krtap9-3<+>	C57BL/6N-Krtap9-3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551155	M	MP:0010097	abnormal retina blood vessel morphology	Lrrc38<em1(IMPC)Tcp>/Lrrc38<em1(IMPC)Tcp>	C57BL/6NCrl-Lrrc38<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551155	M	MP:0002792	abnormal retina vasculature morphology	Lrrc38<em1(IMPC)Tcp>/Lrrc38<em1(IMPC)Tcp>	C57BL/6NCrl-Lrrc38<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551155	F	MP:0001126	abnormal ovary morphology	Lrrc38<em1(IMPC)Tcp>/Lrrc38<em1(IMPC)Tcp>	C57BL/6NCrl-Lrrc38<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551156	F	MP:0010124	decreased bone mineral content	Lrrn3<em1(IMPC)Kmpc>/Lrrn3<em1(IMPC)Kmpc>	C57BL/6NTac-Lrrn3<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551156	F	MP:0000063	decreased bone mineral density	Lrrn3<em1(IMPC)Kmpc>/Lrrn3<em1(IMPC)Kmpc>	C57BL/6NTac-Lrrn3<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551157	F	MP:0000691	enlarged spleen	Ltbp4<em1(IMPC)Tcp>/Ltbp4<em1(IMPC)Tcp>	C57BL/6NCrl-Ltbp4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551157	F	MP:0010053	decreased grip strength	Ltbp4<em1(IMPC)Tcp>/Ltbp4<em1(IMPC)Tcp>	C57BL/6NCrl-Ltbp4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551157	M	MP:0000157	abnormal sternum morphology	Ltbp4<em1(IMPC)Tcp>/Ltbp4<em1(IMPC)Tcp>	C57BL/6NCrl-Ltbp4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551158	M	MP:0010024	increased total body fat amount	Ly6g5b<em1(IMPC)J>/Ly6g5b<em1(IMPC)J>	C57BL/6NJ-Ly6g5b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551158	M	MP:0003961	decreased lean body mass	Ly6g5b<em1(IMPC)J>/Ly6g5b<em1(IMPC)J>	C57BL/6NJ-Ly6g5b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551159	M	MP:0005631	decreased lung weight	Ly86<tm1a(KOMP)Wtsi>/Ly86<+>	C57BL/6N-Ly86<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:7551159	M	MP:0005343	increased circulating aspartate transaminase level	Ly86<tm1a(KOMP)Wtsi>/Ly86<+>	C57BL/6N-Ly86<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:7551159	M	MP:0000218	increased leukocyte cell number	Ly86<tm1a(KOMP)Wtsi>/Ly86<+>	C57BL/6N-Ly86<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:7551159	M	MP:0010025	decreased total body fat amount	Ly86<tm1a(KOMP)Wtsi>/Ly86<+>	C57BL/6N-Ly86<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:7551159	M	MP:0005013	increased lymphocyte cell number	Ly86<tm1a(KOMP)Wtsi>/Ly86<+>	C57BL/6N-Ly86<tm1a(KOMP)Wtsi>/MbpMmucd	N	MGI:5576271
MGI:7551161	F	MP:0005278	abnormal cholesterol homeostasis	Mdm1<em1(IMPC)Kmpc>/Mdm1<em1(IMPC)Kmpc>	C57BL/6NTac-Mdm1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551161	F	MP:0002764	short tibia	Mdm1<em1(IMPC)Kmpc>/Mdm1<em1(IMPC)Kmpc>	C57BL/6NTac-Mdm1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551166	M	MP:0003921	abnormal heart left ventricle morphology	Mir350<tm1Wtsi>/Mir350<tm1Wtsi>	C57BL/6N-Mir350<tm1Wtsi>/Mhzh	N	MGI:5576271
MGI:7551167	F	MP:0002764	short tibia	Mmp13<em1(IMPC)Ccpcz>/Mmp13<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551167	M	MP:0000709	enlarged thymus	Mmp13<em1(IMPC)Ccpcz>/Mmp13<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551167	M	MP:0000689	abnormal spleen morphology	Mmp13<em1(IMPC)Ccpcz>/Mmp13<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551167	M	MP:0000703	abnormal thymus morphology	Mmp13<em1(IMPC)Ccpcz>/Mmp13<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551167	M	MP:0000691	enlarged spleen	Mmp13<em1(IMPC)Ccpcz>/Mmp13<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551167	F	MP:0002968	increased circulating alkaline phosphatase level	Mmp13<em1(IMPC)Ccpcz>/Mmp13<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551167	M	MP:0005333	decreased heart rate	Mmp13<em1(IMPC)Ccpcz>/Mmp13<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551167	M	MP:0010506	prolonged RR interval	Mmp13<em1(IMPC)Ccpcz>/Mmp13<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551167	M	MP:0003233	prolonged QT interval	Mmp13<em1(IMPC)Ccpcz>/Mmp13<em1(IMPC)Ccpcz>	C57BL/6NCrl-Mmp13<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551168	M	MP:0002060	abnormal skin morphology	Mov10<em1(IMPC)Tcp>/Mov10<em1(IMPC)Tcp>	C57BL/6NCrl-Mov10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551168	F	MP:0010097	abnormal retina blood vessel morphology	Mov10<em1(IMPC)Tcp>/Mov10<em1(IMPC)Tcp>	C57BL/6NCrl-Mov10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551168	F	MP:0002792	abnormal retina vasculature morphology	Mov10<em1(IMPC)Tcp>/Mov10<em1(IMPC)Tcp>	C57BL/6NCrl-Mov10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551168	M	MP:0001325	abnormal retina morphology	Mov10<em1(IMPC)Tcp>/Mov10<em1(IMPC)Tcp>	C57BL/6NCrl-Mov10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551168	M	MP:0009142	decreased prepulse inhibition	Mov10<em1(IMPC)Tcp>/Mov10<em1(IMPC)Tcp>	C57BL/6NCrl-Mov10<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551170	M	MP:0000221	decreased leukocyte cell number	Msantd3<em1(IMPC)J>/Msantd3<em1(IMPC)J>	C57BL/6NJ-Msantd3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551172	M	MP:0010024	increased total body fat amount	Nbea<em1(IMPC)Bay>/Nbea<+>	C57BL/6N-Nbea<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551172	M	MP:0000063	decreased bone mineral density	Nbea<em1(IMPC)Bay>/Nbea<+>	C57BL/6N-Nbea<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551173	M	MP:0001488	increased startle reflex	Ncoa7<tm1.1(KOMP)Vlcg>/Ncoa7<tm1.1(KOMP)Vlcg>	C57BL/6N-Ncoa7<tm1.1(KOMP)Vlcg>/Tcp	N	MGI:5576271
MGI:7551174	M	MP:0001556	increased circulating HDL cholesterol level	Nelfcd<em1(IMPC)J>/Nelfcd<+>	C57BL/6NJ-Nelfcd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551174	F	MP:0002591	decreased mean corpuscular volume	Nelfcd<em1(IMPC)J>/Nelfcd<+>	C57BL/6NJ-Nelfcd<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551177	M	MP:0000220	increased monocyte cell number	Nosip<em1(IMPC)Tcp>/Nosip<+>	C57BL/6NCrl-Nosip<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551177	F	MP:0001304	cataract	Nosip<em1(IMPC)Tcp>/Nosip<+>	C57BL/6NCrl-Nosip<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551177	F	MP:0001303	abnormal lens morphology	Nosip<em1(IMPC)Tcp>/Nosip<+>	C57BL/6NCrl-Nosip<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551179	M	MP:0005574	decreased pulmonary respiratory rate	Nudt19<tm1.1(KOMP)Vlcg>/Nudt19<tm1.1(KOMP)Vlcg>	C57BL/6NCrl-Nudt19<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7551180	M	MP:0010025	decreased total body fat amount	Nudt6<em1(IMPC)Bay>/Nudt6<em1(IMPC)Bay>	C57BL/6N-Nudt6<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551180	M	MP:0003960	increased lean body mass	Nudt6<em1(IMPC)Bay>/Nudt6<em1(IMPC)Bay>	C57BL/6N-Nudt6<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551184	F	MP:0001513	limb grasping	Osbpl1a<em1(IMPC)Bay>/Osbpl1a<em1(IMPC)Bay>	C57BL/6N-Osbpl1a<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551185	M	MP:0000266	abnormal heart morphology	Pank2<em1(IMPC)Ccpcz>/Pank2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pank2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551185	M	MP:0001146	abnormal testis morphology	Pank2<em1(IMPC)Ccpcz>/Pank2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pank2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551185	M	MP:0001147	small testis	Pank2<em1(IMPC)Ccpcz>/Pank2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pank2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551185	M	MP:0000274	enlarged heart	Pank2<em1(IMPC)Ccpcz>/Pank2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pank2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551185	M	MP:0001925	male infertility	Pank2<em1(IMPC)Ccpcz>/Pank2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pank2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551185	F	MP:0020421	increased freezing behavior	Pank2<em1(IMPC)Ccpcz>/Pank2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pank2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551185	M	MP:0001417	decreased exploration in new environment	Pank2<em1(IMPC)Ccpcz>/Pank2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pank2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551185	F	MP:0002110	abnormal digit morphology	Pank2<em1(IMPC)Ccpcz>/Pank2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pank2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551185	F	MP:0001926	female infertility	Pank2<em1(IMPC)Ccpcz>/Pank2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pank2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551187	M	MP:0002941	increased circulating alanine transaminase level	Pip<em1(IMPC)Mbp>/Pip<em1(IMPC)Mbp>	C57BL/6NCrl-Pip<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551190	M	MP:0011962	increased cornea thickness	Poldip3<em1(IMPC)Bay>/Poldip3<+>	C57BL/6N-Poldip3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551191	M	MP:0011110	preweaning lethality, incomplete penetrance	Poldip3<em1(IMPC)Bay>/Poldip3<em1(IMPC)Bay>	C57BL/6N-Poldip3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551195	M	MP:0001399	hyperactivity	Prl3d1<em1(IMPC)Bay>/Prl3d1<em1(IMPC)Bay>	C57BL/6N-Prl3d1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551195	F	MP:0011110	preweaning lethality, incomplete penetrance	Prl3d1<em1(IMPC)Bay>/Prl3d1<em1(IMPC)Bay>	C57BL/6N-Prl3d1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551199	F	MP:0001284	absent vibrissae	Rab3il1<em1(IMPC)J>/Rab3il1<em1(IMPC)J>	C57BL/6NJ-Rab3il1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551199	M	MP:0003131	increased erythrocyte cell number	Rab3il1<em1(IMPC)J>/Rab3il1<em1(IMPC)J>	C57BL/6NJ-Rab3il1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551199	M	MP:0001488	increased startle reflex	Rab3il1<em1(IMPC)J>/Rab3il1<em1(IMPC)J>	C57BL/6NJ-Rab3il1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551200	M	MP:0010123	increased bone mineral content	Rabl6<tm1b(KOMP)Wtsi>/Rabl6<tm1b(KOMP)Wtsi>	C57BL/6N-Rabl6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:7551200	M	MP:0000062	increased bone mineral density	Rabl6<tm1b(KOMP)Wtsi>/Rabl6<tm1b(KOMP)Wtsi>	C57BL/6N-Rabl6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:7551200	M	MP:0003960	increased lean body mass	Rabl6<tm1b(KOMP)Wtsi>/Rabl6<tm1b(KOMP)Wtsi>	C57BL/6N-Rabl6<tm1b(KOMP)Wtsi>/Ucd	N	MGI:5576271
MGI:7551201	M	MP:0010052	increased grip strength	Ramac<em1(IMPC)J>/Ramac<+>	C57BL/6NJ-Ramac<em1(IMPC)J>/J	N	MGI:5576271
MGI:7551204	F	MP:0011960	abnormal eye anterior chamber depth	Rundc3b<em1(IMPC)Bay>/Rundc3b<em1(IMPC)Bay>	C57BL/6N-Rundc3b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551204	F	MP:0011965	decreased total retina thickness	Rundc3b<em1(IMPC)Bay>/Rundc3b<em1(IMPC)Bay>	C57BL/6N-Rundc3b<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551207	F	MP:0005278	abnormal cholesterol homeostasis	Saysd1<em1(IMPC)J>/Saysd1<em1(IMPC)J>	C57BL/6NJ-Saysd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551207	M	MP:0000218	increased leukocyte cell number	Saysd1<em1(IMPC)J>/Saysd1<em1(IMPC)J>	C57BL/6NJ-Saysd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551207	F	MP:0011110	preweaning lethality, incomplete penetrance	Saysd1<em1(IMPC)J>/Saysd1<em1(IMPC)J>	C57BL/6NJ-Saysd1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551208	F	MP:0001402	decreased locomotor activity	Scrn1<em1(IMPC)J>/Scrn1<em1(IMPC)J>	C57BL/6NJ-Scrn1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551209	F	MP:0001399	hyperactivity	Sdk1<em1(IMPC)Kmpc>/Sdk1<em1(IMPC)Kmpc>	C57BL/6NTac-Sdk1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551210	M	MP:0009142	decreased prepulse inhibition	Septin2<em1(IMPC)Tcp>/Septin2<+>	C57BL/6NCrl-Septin2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551210	M	MP:0001289	persistence of hyaloid vascular system	Septin2<em1(IMPC)Tcp>/Septin2<+>	C57BL/6NCrl-Septin2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551210	F	MP:0000220	increased monocyte cell number	Septin2<em1(IMPC)Tcp>/Septin2<+>	C57BL/6NCrl-Septin2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551213	F	MP:0011110	preweaning lethality, incomplete penetrance	Sh2d7<tm2b(KOMP)Mbp>/Sh2d7<tm2b(KOMP)Mbp>	C57BL/6N-Sh2d7<tm2b(KOMP)Mbp>/Tcp	N	MGI:5576271
MGI:7551214	F	MP:0005178	increased circulating cholesterol level	Slc10a3<em1(IMPC)J>/Slc10a3<em1(IMPC)J>	C57BL/6NJ-Slc10a3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551216	F	MP:0002591	decreased mean corpuscular volume	Slc27a3<em1(IMPC)Tcp>/Slc27a3<em1(IMPC)Tcp>	C57BL/6NCrl-Slc27a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551216	M	MP:0002060	abnormal skin morphology	Slc27a3<em1(IMPC)Tcp>/Slc27a3<em1(IMPC)Tcp>	C57BL/6NCrl-Slc27a3<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551217	F	MP:0011962	increased cornea thickness	Slc30a6<em1(IMPC)Bay>/Slc30a6<+>	C57BL/6N-Slc30a6<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551222	M	MP:0010067	increased red blood cell distribution width	Slco1b2<em1(IMPC)Mbp>/Slco1b2<em1(IMPC)Mbp>	C57BL/6NCrl-Slco1b2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551222	M	MP:0002092	abnormal eye morphology	Slco1b2<em1(IMPC)Mbp>/Slco1b2<em1(IMPC)Mbp>	C57BL/6NCrl-Slco1b2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551222	F	MP:0002060	abnormal skin morphology	Slco1b2<em1(IMPC)Mbp>/Slco1b2<em1(IMPC)Mbp>	C57BL/6NCrl-Slco1b2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551227	F	MP:0011110	preweaning lethality, incomplete penetrance	Spata21<em1(IMPC)Bay>/Spata21<em1(IMPC)Bay>	C57BL/6N-Spata21<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551227	M	MP:0001513	limb grasping	Spata21<em1(IMPC)Bay>/Spata21<em1(IMPC)Bay>	C57BL/6N-Spata21<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551229	F	MP:0020421	increased freezing behavior	Sstr1<em1(IMPC)Mbp>/Sstr1<em1(IMPC)Mbp>	C57BL/6NCrl-Sstr1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551230	F	MP:0000266	abnormal heart morphology	Sting1<tm1.1(KOMP)Mbp>/Sting1<tm1.1(KOMP)Mbp>	C57BL/6NCrl-Sting1<tm1.1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551230	F	MP:0001926	female infertility	Sting1<tm1.1(KOMP)Mbp>/Sting1<tm1.1(KOMP)Mbp>	C57BL/6NCrl-Sting1<tm1.1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551230	F	MP:0000274	enlarged heart	Sting1<tm1.1(KOMP)Mbp>/Sting1<tm1.1(KOMP)Mbp>	C57BL/6NCrl-Sting1<tm1.1(KOMP)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7551231	F	MP:0011110	preweaning lethality, incomplete penetrance	Strc<em1(IMPC)Bay>/Strc<em1(IMPC)Bay>	C57BL/6N-Strc<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551232	F	MP:0001175	abnormal lung morphology	Sumo1<tm1.1(KOMP)Vlcg>/Sumo1<tm1.1(KOMP)Vlcg>	C57BL/6NCrl-Sumo1<tm1.1(KOMP)Vlcg>/MbpMmucd	N	MGI:5576271
MGI:7551235	F	MP:0002060	abnormal skin morphology	Taok1<em1(IMPC)Tcp>/Taok1<+>	C57BL/6NCrl-Taok1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551237	M	MP:0001325	abnormal retina morphology	Tbc1d25<em1(IMPC)Tcp>/Y	C57BL/6NCrl-Tbc1d25<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551238	F	MP:0010053	decreased grip strength	Tbc1d25<em1(IMPC)Tcp>/Tbc1d25<em1(IMPC)Tcp>	C57BL/6NCrl-Tbc1d25<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551238	F	MP:0001325	abnormal retina morphology	Tbc1d25<em1(IMPC)Tcp>/Tbc1d25<em1(IMPC)Tcp>	C57BL/6NCrl-Tbc1d25<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551239	F	MP:0005554	decreased circulating creatinine level	Tbr1<tm1.1(KOMP)Mbp>/Tbr1<+>	C57BL/6N-Tbr1<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551239	F	MP:0005566	decreased blood urea nitrogen level	Tbr1<tm1.1(KOMP)Mbp>/Tbr1<+>	C57BL/6N-Tbr1<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551239	F	MP:0005560	decreased circulating glucose level	Tbr1<tm1.1(KOMP)Mbp>/Tbr1<+>	C57BL/6N-Tbr1<tm1.1(KOMP)Mbp>/Ucd	N	MGI:5576271
MGI:7551242	M	MP:0000702	enlarged lymph nodes	Thnsl2<em1(IMPC)Tcp>/Thnsl2<em1(IMPC)Tcp>	C57BL/6NCrl-Thnsl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551242	F	MP:0010097	abnormal retina blood vessel morphology	Thnsl2<em1(IMPC)Tcp>/Thnsl2<em1(IMPC)Tcp>	C57BL/6NCrl-Thnsl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551242	M	MP:0002060	abnormal skin morphology	Thnsl2<em1(IMPC)Tcp>/Thnsl2<em1(IMPC)Tcp>	C57BL/6NCrl-Thnsl2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7551243	F	MP:0011110	preweaning lethality, incomplete penetrance	Thsd7b<em1(IMPC)Kmpc>/Thsd7b<em1(IMPC)Kmpc>	C57BL/6NTac-Thsd7b<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551244	F	MP:0000063	decreased bone mineral density	Tmem163<em1(IMPC)Kmpc>/Tmem163<em1(IMPC)Kmpc>	C57BL/6NTac-Tmem163<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551244	F	MP:0003795	abnormal bone structure	Tmem163<em1(IMPC)Kmpc>/Tmem163<em1(IMPC)Kmpc>	C57BL/6NTac-Tmem163<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551244	F	MP:0010124	decreased bone mineral content	Tmem163<em1(IMPC)Kmpc>/Tmem163<em1(IMPC)Kmpc>	C57BL/6NTac-Tmem163<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551244	F	MP:0003961	decreased lean body mass	Tmem163<em1(IMPC)Kmpc>/Tmem163<em1(IMPC)Kmpc>	C57BL/6NTac-Tmem163<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551244	M	MP:0002075	abnormal coat/hair pigmentation	Tmem163<em1(IMPC)Kmpc>/Tmem163<em1(IMPC)Kmpc>	C57BL/6NTac-Tmem163<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551244	F	MP:0010024	increased total body fat amount	Tmem163<em1(IMPC)Kmpc>/Tmem163<em1(IMPC)Kmpc>	C57BL/6NTac-Tmem163<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551252	M	MP:0001399	hyperactivity	Tspan5<em1(IMPC)Kmpc>/Tspan5<em1(IMPC)Kmpc>	C57BL/6NTac-Tspan5<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7551257	F	MP:0001325	abnormal retina morphology	Vps36<em1(IMPC)J>/Vps36<+>	C57BL/6NJ-Vps36<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551259	M	MP:0003394	increased cardiac output	Wdr27<em1(IMPC)Ccpcz>/Wdr27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Wdr27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551259	M	MP:0003179	thrombocytopenia	Wdr27<em1(IMPC)Ccpcz>/Wdr27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Wdr27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551259	M	MP:0005343	increased circulating aspartate transaminase level	Wdr27<em1(IMPC)Ccpcz>/Wdr27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Wdr27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551259	M	MP:0010574	dilated aorta	Wdr27<em1(IMPC)Ccpcz>/Wdr27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Wdr27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551259	M	MP:0002953	thick ventricular wall	Wdr27<em1(IMPC)Ccpcz>/Wdr27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Wdr27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551259	M	MP:0010067	increased red blood cell distribution width	Wdr27<em1(IMPC)Ccpcz>/Wdr27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Wdr27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551259	F	MP:0008810	increased circulating iron level	Wdr27<em1(IMPC)Ccpcz>/Wdr27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Wdr27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551259	M	MP:0005179	decreased circulating cholesterol level	Wdr27<em1(IMPC)Ccpcz>/Wdr27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Wdr27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551259	F	MP:0001325	abnormal retina morphology	Wdr27<em1(IMPC)Ccpcz>/Wdr27<em1(IMPC)Ccpcz>	C57BL/6NCrl-Wdr27<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7551260	F	MP:0003795	abnormal bone structure	Wwc2<em1(IMPC)Bay>/Wwc2<+>	C57BL/6N-Wwc2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551261	M	MP:0011100	preweaning lethality, complete penetrance	Wwc2<em1(IMPC)Bay>/Wwc2<em1(IMPC)Bay>	C57BL/6N-Wwc2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551261	M	MP:0001925	male infertility	Wwc2<em1(IMPC)Bay>/Wwc2<em1(IMPC)Bay>	C57BL/6N-Wwc2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7551264	M	MP:0000208	decreased hematocrit	Zfp28<em1(IMPC)J>/Zfp28<em1(IMPC)J>	C57BL/6NJ-Zfp28<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551264	M	MP:0002875	decreased erythrocyte cell number	Zfp28<em1(IMPC)J>/Zfp28<em1(IMPC)J>	C57BL/6NJ-Zfp28<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551267	F	MP:0002965	increased circulating serum albumin level	Zfp691<em1(IMPC)J>/Zfp691<em1(IMPC)J>	C57BL/6NJ-Zfp691<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7551271	M	MP:0001417	decreased exploration in new environment	Znrf2<em1(IMPC)Bay>/Znrf2<em1(IMPC)Bay>	C57BL/6N-Znrf2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7560635	F	MP:0003718	maternal effect	H1f1<em1Ibbr>/H1f1<em1Ibbr>	C57BL/6J-H1f1<em1Ibbr>	N	37062716
MGI:7560663	M	MP:0014052	increased male germ cell apoptosis	Btbd18<tm1Dean>/Btbd18<tm1Dean>	involves: 129S4/SvJae * C57BL/6	N	28292424
MGI:7560663	M	MP:0004901	decreased male germ cell number	Btbd18<tm1Dean>/Btbd18<tm1Dean>	involves: 129S4/SvJae * C57BL/6	N	28292424
MGI:7560663	M	MP:0001929	abnormal gametogenesis	Btbd18<tm1Dean>/Btbd18<tm1Dean>	involves: 129S4/SvJae * C57BL/6	N	28292424
MGI:7560663	M	MP:0006380	abnormal spermatid morphology	Btbd18<tm1Dean>/Btbd18<tm1Dean>	involves: 129S4/SvJae * C57BL/6	N	28292424
MGI:7560663	M	MP:0008279	arrest of spermiogenesis	Btbd18<tm1Dean>/Btbd18<tm1Dean>	involves: 129S4/SvJae * C57BL/6	N	28292424
MGI:7560663	M	MP:0013601	increased testis apoptosis	Btbd18<tm1Dean>/Btbd18<tm1Dean>	involves: 129S4/SvJae * C57BL/6	N	28292424
MGI:7560663	M	MP:0001155	arrest of spermatogenesis	Btbd18<tm1Dean>/Btbd18<tm1Dean>	involves: 129S4/SvJae * C57BL/6	N	28292424
MGI:7560663	M	MP:0005159	azoospermia	Btbd18<tm1Dean>/Btbd18<tm1Dean>	involves: 129S4/SvJae * C57BL/6	N	28292424
MGI:7560663	M	MP:0001925	male infertility	Btbd18<tm1Dean>/Btbd18<tm1Dean>	involves: 129S4/SvJae * C57BL/6	N	28292424
MGI:7560663	M	MP:0004852	decreased testis weight	Btbd18<tm1Dean>/Btbd18<tm1Dean>	involves: 129S4/SvJae * C57BL/6	N	28292424
MGI:7560663	M	MP:0001147	small testis	Btbd18<tm1Dean>/Btbd18<tm1Dean>	involves: 129S4/SvJae * C57BL/6	N	28292424
MGI:7562295	M	MP:0004946	abnormal regulatory T cell physiology	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0002083	premature death	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0008681	increased interleukin-17 secretion	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0011631	decreased mitochondrial size	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0005018	decreased T cell number	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0006035	abnormal mitochondrial morphology	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0012188	increased regulatory T cell apoptosis	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0008019	increased liver tumor incidence	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0004974	decreased regulatory T cell number	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0002941	increased circulating alanine transaminase level	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0006036	abnormal mitochondrial physiology	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0008049	increased memory T cell number	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0008078	increased CD8-positive, alpha-beta T cell number	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0031269	increased susceptibility to diet-induced hepatic steatosis	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0000598	abnormal liver morphology	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7562295	M	MP:0003333	liver fibrosis	Altre<tm1.1Hbgl>/Altre<tm1.1Hbgl>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	37277640
MGI:7564143	M	MP:0005455	increased susceptibility to weight gain	Mir10b<em1Rosay>/Mir10b<em1Rosay>	C57BL/6J-Mir10b<em1Rosay>	N	37723933
MGI:7564549	M	MP:0005283	increased unsaturated fatty acids level	Tmlhe<em1Plaa>/Tmlhe<em1Plaa>	C57BL/6N-Tmlhe<em1Plaa>	N	34728372
MGI:7564549	M	MP:0005281	increased fatty acids level	Tmlhe<em1Plaa>/Tmlhe<em1Plaa>	C57BL/6N-Tmlhe<em1Plaa>	N	34728372
MGI:7564549	M	MP:0000278	abnormal myocardial fiber morphology	Tmlhe<em1Plaa>/Tmlhe<em1Plaa>	C57BL/6N-Tmlhe<em1Plaa>	N	34728372
MGI:7564549	M	MP:0003038	decreased myocardial infarct size	Tmlhe<em1Plaa>/Tmlhe<em1Plaa>	C57BL/6N-Tmlhe<em1Plaa>	N	34728372
MGI:7564549	M	MP:0006036	abnormal mitochondrial physiology	Tmlhe<em1Plaa>/Tmlhe<em1Plaa>	C57BL/6N-Tmlhe<em1Plaa>	N	34728372
MGI:7564549	M	MP:0013404	decreased circulating lactate level	Tmlhe<em1Plaa>/Tmlhe<em1Plaa>	C57BL/6N-Tmlhe<em1Plaa>	N	34728372
MGI:7564549	M	MP:0014172	decreased fatty acid oxidation	Tmlhe<em1Plaa>/Tmlhe<em1Plaa>	C57BL/6N-Tmlhe<em1Plaa>	N	34728372
MGI:7564549	M	MP:0003978	decreased circulating carnitine level	Tmlhe<em1Plaa>/Tmlhe<em1Plaa>	C57BL/6N-Tmlhe<em1Plaa>	N	34728372
MGI:7564549	M	MP:0000343	abnormal response to cardiac infarction	Tmlhe<em1Plaa>/Tmlhe<em1Plaa>	C57BL/6N-Tmlhe<em1Plaa>	N	34728372
MGI:7564549	M	MP:0000266	abnormal heart morphology	Tmlhe<em1Plaa>/Tmlhe<em1Plaa>	C57BL/6N-Tmlhe<em1Plaa>	N	34728372
MGI:7564549	M	MP:0005386	behavior/neurological phenotype	Tmlhe<em1Plaa>/Tmlhe<em1Plaa>	C57BL/6N-Tmlhe<em1Plaa>	Y	34728372
MGI:7564549	M	MP:0005280	abnormal fatty acids level	Tmlhe<em1Plaa>/Tmlhe<em1Plaa>	C57BL/6N-Tmlhe<em1Plaa>	N	34728372
MGI:7564549	M	MP:0004215	abnormal myocardial fiber physiology	Tmlhe<em1Plaa>/Tmlhe<em1Plaa>	C57BL/6N-Tmlhe<em1Plaa>	N	34728372
MGI:7565493	M	MP:0031215	abnormal response to myocardial ischemic injury	Swhtr<tm1.1Phg>/Swhtr<tm1.1Phg>	either: (involves: C57BL/6J) or (involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac)	N	37919291
MGI:7565493	M	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality	Swhtr<tm1.1Phg>/Swhtr<tm1.1Phg>	either: (involves: C57BL/6J) or (involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac)	N	37919291
MGI:7567453	M	MP:0014256	decreased paired-pulse inhibition	Mir501<tm1Rchen>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	35984881
MGI:7567453	M	MP:0020508	decreased dendritic spine density	Mir501<tm1Rchen>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	35984881
MGI:7567453	M	MP:0020335	abnormal dentate gyrus neuron dendrite morphology	Mir501<tm1Rchen>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	35984881
MGI:7567453	M	MP:0014378	increased excitatory postsynaptic current frequency	Mir501<tm1Rchen>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	35984881
MGI:7567453	M	MP:0021111	decreased social investigation	Mir501<tm1Rchen>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	35984881
MGI:7567453	M	MP:0021009	abnormal synaptic physiology	Mir501<tm1Rchen>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	35984881
MGI:7567453	M	MP:0020395	abnormal response to social novelty	Mir501<tm1Rchen>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	35984881
MGI:7567453	M	MP:0012006	abnormal hippocampus physiology	Mir501<tm1Rchen>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	35984881
MGI:7567453	M	MP:0003461	abnormal response to novel object	Mir501<tm1Rchen>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	N	35984881
MGI:7568838	M	MP:0005378	growth/size/body region phenotype	Trim72<tm1Rpx>/Trim72<tm1Rpx>	involves: 129/SvJ * C57BL/6	Y	34844991
MGI:7568838	M	MP:0005369	muscle phenotype	Trim72<tm1Rpx>/Trim72<tm1Rpx>	involves: 129/SvJ * C57BL/6	Y	34844991
MGI:7568838	M	MP:0005376	homeostasis/metabolism phenotype	Trim72<tm1Rpx>/Trim72<tm1Rpx>	involves: 129/SvJ * C57BL/6	Y	34844991
MGI:7568838	M	MP:0005659	decreased susceptibility to diet-induced obesity	Trim72<tm1Rpx>/Trim72<tm1Rpx>	involves: 129/SvJ * C57BL/6	N	34844991
MGI:7568838	M	MP:0002323	decreased susceptibility to hyperlipidemia	Trim72<tm1Rpx>/Trim72<tm1Rpx>	involves: 129/SvJ * C57BL/6	N	34844991
MGI:7568838	M	MP:0020090	decreased susceptibility to diet-induced non-insulin dependent diabetes	Trim72<tm1Rpx>/Trim72<tm1Rpx>	involves: 129/SvJ * C57BL/6	N	34844991
MGI:7568838	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Trim72<tm1Rpx>/Trim72<tm1Rpx>	involves: 129/SvJ * C57BL/6	N	34844991
MGI:7568838	M	MP:0005385	cardiovascular system phenotype	Trim72<tm1Rpx>/Trim72<tm1Rpx>	involves: 129/SvJ * C57BL/6	Y	34844991
MGI:7569326	M	MP:0001925	male infertility	Dnaaf5<em1Slb>/Dnaaf5<em1Slb>	C57BL/6-Dnaaf5<em1Slb>	N	37104040
MGI:7569326	M	MP:0020869	immotile sperm	Dnaaf5<em1Slb>/Dnaaf5<em1Slb>	C57BL/6-Dnaaf5<em1Slb>	N	37104040
MGI:7569326	F	MP:0005384	cellular phenotype	Dnaaf5<em1Slb>/Dnaaf5<em1Slb>	C57BL/6-Dnaaf5<em1Slb>	Y	37104040
MGI:7569326	F	MP:0005389	reproductive system phenotype	Dnaaf5<em1Slb>/Dnaaf5<em1Slb>	C57BL/6-Dnaaf5<em1Slb>	Y	37104040
MGI:7571249	M	MP:0009732	ventricular premature beat	Dsg2<em1Spin>/Dsg2<+>	involves: C57BL/6J	N	36268721
MGI:7576214	F	MP:0002566	abnormal sexual interaction	Ccdc28b<em1Jlba>/Ccdc28b<em1Jlba>	C57BL/6J-Ccdc28b<em1Jlba>	N	35653384
MGI:7577000	M	MP:0014336	short retina rod cell outer segment	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0001325	abnormal retina morphology	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0003674	oxidative stress	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0031606	increased susceptibility to age-related retinal degeneration	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0003733	abnormal retina inner nuclear layer morphology	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0003729	abnormal photoreceptor outer segment morphology	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0003730	abnormal photoreceptor inner segment morphology	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0005253	abnormal eye physiology	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0012143	decreased a-wave amplitude	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0008449	abnormal retina cone cell outer segment morphology	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0002698	abnormal sclera morphology	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0003734	abnormal retina inner plexiform layer morphology	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0020448	increased microglial cell activation	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0011965	decreased total retina thickness	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0012029	abnormal electroretinogram waveform feature	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0003690	abnormal glial cell physiology	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0005201	abnormal retina pigment epithelium morphology	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0008515	thin retina outer nuclear layer	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0013245	abnormal lipid metabolism	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0006187	retina deposits	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0008450	retina photoreceptor degeneration	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577000	M	MP:0012144	decreased b-wave amplitude	Cyp4v3<em1Xsu>/Cyp4v3<em1Xsu>	C57BL/6J-Cyp4v3<em1Xsu>	N	35230417
MGI:7577474	M	MP:0031373	abnormal manchette perinuclear ring morphology	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0009239	short sperm flagellum	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0031386	elongated manchette	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0031356	abnormal outer dense fiber morphology	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0009376	abnormal manchette morphology	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0008545	absent sperm flagellum	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0001925	male infertility	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0020869	immotile sperm	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0009238	coiled sperm flagellum	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0001932	abnormal spermiogenesis	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0005578	teratozoospermia	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0009838	abnormal sperm axoneme morphology	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0002687	oligozoospermia	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0008892	abnormal sperm flagellum morphology	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7577474	M	MP:0009230	abnormal sperm head morphology	Ccdc146<em1Cya>/Ccdc146<em1Cya>	Not Specified	N	38038747
MGI:7578782	M	MP:0003724	increased susceptibility to induced arthritis	Myl3<tm1a(EUCOMM)Hmgu>/Myl3<tm1a(EUCOMM)Hmgu>,Tg(Col2a1-cre/ERT)KA3Smac/0	involves: C57BL/6J * C57BL/6N * FVB/N	N	37794006
MGI:7579102	F	MP:0001496	audiogenic seizures	Hnrnph2<em1Jpat>/Hnrnph2<+>	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7579102	F	MP:0000097	short maxilla	Hnrnph2<em1Jpat>/Hnrnph2<+>	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7579102	F	MP:0001891	hydrocephaly	Hnrnph2<em1Jpat>/Hnrnph2<+>	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7579102	F	MP:0008525	decreased cranium height	Hnrnph2<em1Jpat>/Hnrnph2<+>	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7579102	F	MP:0001405	impaired coordination	Hnrnph2<em1Jpat>/Hnrnph2<+>	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7579102	F	MP:0000445	short snout	Hnrnph2<em1Jpat>/Hnrnph2<+>	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7579102	F	MP:0000428	abnormal craniofacial morphology	Hnrnph2<em1Jpat>/Hnrnph2<+>	C57BL/6J-Hnrnph2<em1Jpat>	N	37463454
MGI:7579105	F	MP:0001496	audiogenic seizures	Hnrnph2<em2Jpat>/Hnrnph2<em2Jpat>	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7579106	F	MP:0001891	hydrocephaly	Hnrnph2<em2Jpat>/Hnrnph2<+>	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7579106	F	MP:0005537	abnormal cerebral aqueduct morphology	Hnrnph2<em2Jpat>/Hnrnph2<+>	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7579106	F	MP:0001262	decreased body weight	Hnrnph2<em2Jpat>/Hnrnph2<+>	C57BL/6J-Hnrnph2<em2Jpat>	N	37463454
MGI:7579276	F	MP:0001405	impaired coordination	Morc2a<em1Snupy>/Morc2a<+>	involves: C57BL/6	N	34695197
MGI:7579276	F	MP:0001402	decreased locomotor activity	Morc2a<em1Snupy>/Morc2a<+>	involves: C57BL/6	N	34695197
MGI:7580443	M	MP:0005331	insulin resistance	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0005658	increased susceptibility to diet-induced obesity	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0030017	decreased adipocyte glucose uptake	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0008964	decreased carbon dioxide production	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0009288	increased epididymal fat pad weight	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0005293	impaired glucose tolerance	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0009118	increased white fat cell size	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0005584	abnormal enzyme/coenzyme activity	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0008469	abnormal protein level	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0031600	increased white adipose tissue apoptosis	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0005290	decreased oxygen consumption	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0031602	white adipose tissue inflammation	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0001552	increased circulating triglyceride level	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0009292	increased inguinal fat pad weight	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0005670	abnormal white adipose tissue physiology	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7580443	M	MP:0004890	decreased energy expenditure	Serpina3c<em1Smoc>/Serpina3c<em1Smoc>	C57BL/6-Serpina3c<em1Smoc>	N	35436587
MGI:7581907	M	MP:0001762	polyuria	Slc38a2<em1Zhxy>/Slc38a2<em1Zhxy>	129.B6-Slc38a2<em1Zhxy>	N	36722887
MGI:7581907	M	MP:0012605	decreased kidney glutathione level	Slc38a2<em1Zhxy>/Slc38a2<em1Zhxy>	129.B6-Slc38a2<em1Zhxy>	N	36722887
MGI:7581907	M	MP:0012659	decreased superoxide dismutase level	Slc38a2<em1Zhxy>/Slc38a2<em1Zhxy>	129.B6-Slc38a2<em1Zhxy>	N	36722887
MGI:7581907	M	MP:0014359	increased ferroptosis	Slc38a2<em1Zhxy>/Slc38a2<em1Zhxy>	129.B6-Slc38a2<em1Zhxy>	N	36722887
MGI:7581907	M	MP:0010375	increased kidney iron level	Slc38a2<em1Zhxy>/Slc38a2<em1Zhxy>	129.B6-Slc38a2<em1Zhxy>	N	36722887
MGI:7581907	M	MP:0008055	increased urine osmolality	Slc38a2<em1Zhxy>/Slc38a2<em1Zhxy>	129.B6-Slc38a2<em1Zhxy>	N	36722887
MGI:7581907	M	MP:0002135	abnormal kidney morphology	Slc38a2<em1Zhxy>/Slc38a2<em1Zhxy>	129.B6-Slc38a2<em1Zhxy>	N	36722887
MGI:7587853	M	MP:0009838	abnormal sperm axoneme morphology	Cfap70<em1Chnsr>/Cfap70<em1Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587853	M	MP:0002675	asthenozoospermia	Cfap70<em1Chnsr>/Cfap70<em1Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587853	M	MP:0031356	abnormal outer dense fiber morphology	Cfap70<em1Chnsr>/Cfap70<em1Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587853	M	MP:0001925	male infertility	Cfap70<em1Chnsr>/Cfap70<em1Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587853	M	MP:0009238	coiled sperm flagellum	Cfap70<em1Chnsr>/Cfap70<em1Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587853	M	MP:0008892	abnormal sperm flagellum morphology	Cfap70<em1Chnsr>/Cfap70<em1Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587853	M	MP:0009239	short sperm flagellum	Cfap70<em1Chnsr>/Cfap70<em1Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587853	M	MP:0002687	oligozoospermia	Cfap70<em1Chnsr>/Cfap70<em1Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587862	M	MP:0009838	abnormal sperm axoneme morphology	Cfap70<em2Chnsr>/Cfap70<em2Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587862	M	MP:0008892	abnormal sperm flagellum morphology	Cfap70<em2Chnsr>/Cfap70<em2Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587862	M	MP:0002687	oligozoospermia	Cfap70<em2Chnsr>/Cfap70<em2Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587862	M	MP:0009238	coiled sperm flagellum	Cfap70<em2Chnsr>/Cfap70<em2Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587862	M	MP:0002675	asthenozoospermia	Cfap70<em2Chnsr>/Cfap70<em2Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587862	M	MP:0001925	male infertility	Cfap70<em2Chnsr>/Cfap70<em2Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587862	M	MP:0008545	absent sperm flagellum	Cfap70<em2Chnsr>/Cfap70<em2Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587862	M	MP:0031352	absent sperm axonemal central pair	Cfap70<em2Chnsr>/Cfap70<em2Chnsr>	involves: C57BL/6J	N	37352829
MGI:7587862	M	MP:0009239	short sperm flagellum	Cfap70<em2Chnsr>/Cfap70<em2Chnsr>	involves: C57BL/6J	N	37352829
MGI:7593606	M	MP:0009289	decreased epididymal fat pad weight	Apol6<em1Hsul>/Apol6<em1Hsul>	Not Specified	N	38167864
MGI:7593625	M	MP:0009288	increased epididymal fat pad weight	Tg(Adipoq-Apol6)#Hsul/0	C57BL/6J-Tg(Adipoq-Apol6)#Hsul	N	38167864
MGI:7593628	M	MP:0009288	increased epididymal fat pad weight	Tg(Fabp4-Apol6)#Hsul/0	C57BL/6J-Tg(Fabp4-Apol6)#Hsul	N	38167864
MGI:7593773	M	MP:0006001	abnormal intestinal transit time	Actg2<em1Yiwan>/Actg2<+>	involves: C57BL/6J	N	36264152
MGI:7593981	M	MP:0001925	male infertility	Tbc1d20<em1Djsi>/Tbc1d20<em1Djsi>	involves: C57BL/6 * DBA/2	N	25476608
MGI:7593981	M	MP:0001147	small testis	Tbc1d20<em1Djsi>/Tbc1d20<em1Djsi>	involves: C57BL/6 * DBA/2	N	25476608
MGI:7593981	M	MP:0031354	abnormal acrosome assembly	Tbc1d20<em1Djsi>/Tbc1d20<em1Djsi>	involves: C57BL/6 * DBA/2	N	25476608
MGI:7593981	M	MP:0002216	abnormal seminiferous tubule morphology	Tbc1d20<em1Djsi>/Tbc1d20<em1Djsi>	involves: C57BL/6 * DBA/2	N	25476608
MGI:7595996	F	MP:0002309	abnormal vital capacity	Pald1<tm1Vlcg>/Pald1<tm1Vlcg>	B6.Cg-Pald1<tm1Vlcg>	N	29133847
MGI:7595996	F	MP:0010937	increased total lung capacity	Pald1<tm1Vlcg>/Pald1<tm1Vlcg>	B6.Cg-Pald1<tm1Vlcg>	N	29133847
MGI:7595996	F	MP:0001942	abnormal lung volume	Pald1<tm1Vlcg>/Pald1<tm1Vlcg>	B6.Cg-Pald1<tm1Vlcg>	N	29133847
MGI:7595996	F	MP:0010895	increased lung compliance	Pald1<tm1Vlcg>/Pald1<tm1Vlcg>	B6.Cg-Pald1<tm1Vlcg>	N	29133847
MGI:7595996	F	MP:0011139	increased lung endothelial cell proliferation	Pald1<tm1Vlcg>/Pald1<tm1Vlcg>	B6.Cg-Pald1<tm1Vlcg>	N	29133847
MGI:7595996	F	MP:0010936	decreased airway resistance	Pald1<tm1Vlcg>/Pald1<tm1Vlcg>	B6.Cg-Pald1<tm1Vlcg>	N	29133847
MGI:7595996	F	MP:0001183	overexpanded pulmonary alveolus	Pald1<tm1Vlcg>/Pald1<tm1Vlcg>	B6.Cg-Pald1<tm1Vlcg>	N	29133847
MGI:7595996	F	MP:0011141	increased lung endothelial cell apoptosis	Pald1<tm1Vlcg>/Pald1<tm1Vlcg>	B6.Cg-Pald1<tm1Vlcg>	N	29133847
MGI:7595996	F	MP:0001958	emphysema	Pald1<tm1Vlcg>/Pald1<tm1Vlcg>	B6.Cg-Pald1<tm1Vlcg>	N	29133847
MGI:7595996	F	MP:0006057	decreased vascular endothelial cell number	Pald1<tm1Vlcg>/Pald1<tm1Vlcg>	B6.Cg-Pald1<tm1Vlcg>	N	29133847
MGI:7596040	F	MP:0001183	overexpanded pulmonary alveolus	Pald1<tm1Vlcg>/Pald1<+>	B6.Cg-Pald1<tm1Vlcg>	N	29133847
MGI:7596132	M	MP:0031386	elongated manchette	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0008898	abnormal acrosome morphology	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0009230	abnormal sperm head morphology	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0008892	abnormal sperm flagellum morphology	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0014465	abnormal sperm mitochondrial morphology	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0002675	asthenozoospermia	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0001147	small testis	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0009238	coiled sperm flagellum	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0001932	abnormal spermiogenesis	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0005578	teratozoospermia	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0009239	short sperm flagellum	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0001925	male infertility	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0004852	decreased testis weight	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0009838	abnormal sperm axoneme morphology	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0030590	abnormal sperm fibrous sheath morphology	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0031374	abnormal manchette assembly	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596132	M	MP:0002687	oligozoospermia	Cfap119<em1Gaof>/Cfap119<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596136	M	MP:0005389	reproductive system phenotype	Cfap119<em2Gaof>/Cfap119<em2Gaof>	involves: 129/SvEv * C57BL/6	Y	37601242
MGI:7596137	M	MP:0005389	reproductive system phenotype	Cfap119<em1Gaof>/Cfap119<em2Gaof>	involves: 129/SvEv * C57BL/6	Y	37601242
MGI:7596138	M	MP:0008892	abnormal sperm flagellum morphology	Cabcoco1<em1Gaof>/Cabcoco1<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596138	M	MP:0005578	teratozoospermia	Cabcoco1<em1Gaof>/Cabcoco1<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596138	M	MP:0001932	abnormal spermiogenesis	Cabcoco1<em1Gaof>/Cabcoco1<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596138	M	MP:0002675	asthenozoospermia	Cabcoco1<em1Gaof>/Cabcoco1<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596138	M	MP:0002687	oligozoospermia	Cabcoco1<em1Gaof>/Cabcoco1<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596138	M	MP:0008545	absent sperm flagellum	Cabcoco1<em1Gaof>/Cabcoco1<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596138	M	MP:0009239	short sperm flagellum	Cabcoco1<em1Gaof>/Cabcoco1<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596138	M	MP:0001925	male infertility	Cabcoco1<em1Gaof>/Cabcoco1<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596138	M	MP:0009238	coiled sperm flagellum	Cabcoco1<em1Gaof>/Cabcoco1<em1Gaof>	involves: 129/SvEv * C57BL/6	N	37601242
MGI:7596332	M	MP:0002573	behavioral despair	Vrk2<em9Gpt>/Vrk2<em9Gpt>	C57BL/6J-Vrk2<em9Gpt>	N	37452335
MGI:7596332	M	MP:0020512	abnormal dendritic mushroom spine morphology	Vrk2<em9Gpt>/Vrk2<em9Gpt>	C57BL/6J-Vrk2<em9Gpt>	N	37452335
MGI:7596332	M	MP:0021010	impaired synaptic physiology	Vrk2<em9Gpt>/Vrk2<em9Gpt>	C57BL/6J-Vrk2<em9Gpt>	N	37452335
MGI:7596332	M	MP:0020514	abnormal dendritic thin spine morphology	Vrk2<em9Gpt>/Vrk2<em9Gpt>	C57BL/6J-Vrk2<em9Gpt>	N	37452335
MGI:7596332	M	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology	Vrk2<em9Gpt>/Vrk2<em9Gpt>	C57BL/6J-Vrk2<em9Gpt>	N	37452335
MGI:7596332	M	MP:0005386	behavior/neurological phenotype	Vrk2<em9Gpt>/Vrk2<em9Gpt>	C57BL/6J-Vrk2<em9Gpt>	Y	37452335
MGI:7596572	F	MP:0000689	abnormal spleen morphology	Vcan<em2(IMPC)Mbp>/Vcan<+>	C57BL/6NCrl-Vcan<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:7596572	F	MP:0006203	eye hemorrhage	Vcan<em2(IMPC)Mbp>/Vcan<+>	C57BL/6NCrl-Vcan<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:7596572	F	MP:0002092	abnormal eye morphology	Vcan<em2(IMPC)Mbp>/Vcan<+>	C57BL/6NCrl-Vcan<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:7596572	F	MP:0000691	enlarged spleen	Vcan<em2(IMPC)Mbp>/Vcan<+>	C57BL/6NCrl-Vcan<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:7596573	M	MP:0002151	abnormal neural tube morphology	Vcan<em2(IMPC)Mbp>/Vcan<em2(IMPC)Mbp>	C57BL/6NCrl-Vcan<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:7596573	F	MP:0003425	abnormal optic vesicle formation	Vcan<em2(IMPC)Mbp>/Vcan<em2(IMPC)Mbp>	C57BL/6NCrl-Vcan<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:7596573	F	MP:0002884	abnormal pharyngeal arch morphology	Vcan<em2(IMPC)Mbp>/Vcan<em2(IMPC)Mbp>	C57BL/6NCrl-Vcan<em2(IMPC)Mbp>/Mmucd	N	MGI:5576271
MGI:7607206	M	MP:0002941	increased circulating alanine transaminase level	Orm2<em1Bcgen>/Orm2<+>	involves: C57BL/6J	N	36050503
MGI:7607206	M	MP:0009355	increased liver triglyceride level	Orm2<em1Bcgen>/Orm2<+>	involves: C57BL/6J	N	36050503
MGI:7607206	M	MP:0001552	increased circulating triglyceride level	Orm2<em1Bcgen>/Orm2<+>	involves: C57BL/6J	N	36050503
MGI:7608027	F	MP:0001935	decreased litter size	Ak9<em1Mdj>/Ak9<em1Mdj>	C57BL/6-Ak9<em1Mdj>	N	38100419
MGI:7608027	M	MP:0001925	male infertility	Ak9<em1Mdj>/Ak9<em1Mdj>	C57BL/6-Ak9<em1Mdj>	N	38100419
MGI:7608027	M	MP:0001924	infertility	Ak9<em1Mdj>/Ak9<em1Mdj>	C57BL/6-Ak9<em1Mdj>	N	38100419
MGI:7608027	F	MP:0005389	reproductive system phenotype	Ak9<em1Mdj>/Ak9<em1Mdj>	C57BL/6-Ak9<em1Mdj>	Y	38100419
MGI:7608027	M	MP:0002674	abnormal sperm motility	Ak9<em1Mdj>/Ak9<em1Mdj>	C57BL/6-Ak9<em1Mdj>	N	38100419
MGI:7608097	M	MP:0002644	decreased circulating triglyceride level	Pycr1<tm1(KOMP)Vlcg>/Pycr1<tm1(KOMP)Vlcg>	C57BL/6NTac-Pycr1<tm1(KOMP)Vlcg>	N	33734376
MGI:7608097	M	MP:0005293	impaired glucose tolerance	Pycr1<tm1(KOMP)Vlcg>/Pycr1<tm1(KOMP)Vlcg>	C57BL/6NTac-Pycr1<tm1(KOMP)Vlcg>	N	33734376
MGI:7608099	M	MP:0010955	abnormal respiratory electron transport chain	Slc41a1<tm1.1Geno>/Slc41a1<tm1.1Geno>	involves: C57BL/6	N	33153064
MGI:7608099	M	MP:0010958	abnormal tricarboxylic acid cycle	Slc41a1<tm1.1Geno>/Slc41a1<tm1.1Geno>	involves: C57BL/6	N	33153064
MGI:7608107	F	MP:0001926	female infertility	Cdc23<em1Lwa>/Cdc23<em1Lwa>	C57BL/6N-Cdc23<em1Lwa>	N	37768355
MGI:7608107	F	MP:0010767	abnormal female meiosis I arrest	Cdc23<em1Lwa>/Cdc23<em1Lwa>	C57BL/6N-Cdc23<em1Lwa>	N	37768355
MGI:7610682	M	MP:0005293	impaired glucose tolerance	Gpcpd1<tm1c(EUCOMM)Hmgu>/Gpcpd1<tm1c(EUCOMM)Hmgu>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6J * C57BL/6N * FVB	N	38238601
MGI:7610682	M	MP:0030018	increased cardiac muscle cell glucose uptake	Gpcpd1<tm1c(EUCOMM)Hmgu>/Gpcpd1<tm1c(EUCOMM)Hmgu>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6J * C57BL/6N * FVB	N	38238601
MGI:7610682	M	MP:0014068	abnormal muscle glycogen level	Gpcpd1<tm1c(EUCOMM)Hmgu>/Gpcpd1<tm1c(EUCOMM)Hmgu>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6J * C57BL/6N * FVB	N	38238601
MGI:7610682	M	MP:0005376	homeostasis/metabolism phenotype	Gpcpd1<tm1c(EUCOMM)Hmgu>/Gpcpd1<tm1c(EUCOMM)Hmgu>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6J * C57BL/6N * FVB	Y	38238601
MGI:7610682	M	MP:0030021	increased muscle cell glucose uptake	Gpcpd1<tm1c(EUCOMM)Hmgu>/Gpcpd1<tm1c(EUCOMM)Hmgu>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6J * C57BL/6N * FVB	N	38238601
MGI:7610682	M	MP:0001559	hyperglycemia	Gpcpd1<tm1c(EUCOMM)Hmgu>/Gpcpd1<tm1c(EUCOMM)Hmgu>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6J * C57BL/6N * FVB	N	38238601
MGI:7610682	M	MP:0005369	muscle phenotype	Gpcpd1<tm1c(EUCOMM)Hmgu>/Gpcpd1<tm1c(EUCOMM)Hmgu>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6J * C57BL/6N * FVB	Y	38238601
MGI:7610682	M	MP:0003058	increased insulin secretion	Gpcpd1<tm1c(EUCOMM)Hmgu>/Gpcpd1<tm1c(EUCOMM)Hmgu>,Tg(Ckmm-cre)5Khn/0	involves: C57BL/6J * C57BL/6N * FVB	N	38238601
MGI:7610684	M	MP:0005376	homeostasis/metabolism phenotype	Gpcpd1<tm1c(EUCOMM)Hmgu>/Gpcpd1<tm1c(EUCOMM)Hmgu>,Speer6-ps1<Tg(Alb-cre)21Mgn>/Speer6-ps1<+>	involves: C57BL/6 * DBA	Y	38238601
MGI:7610685	M	MP:0005376	homeostasis/metabolism phenotype	Gpcpd1<tm1c(EUCOMM)Hmgu>/Gpcpd1<tm1c(EUCOMM)Hmgu>,Tg(Fabp4-cre)1Rev/0	involves: C57BL/6J * C57BL/6N	N	38238601
MGI:7610686	M	MP:0005376	homeostasis/metabolism phenotype	Gpcpd1<tm1c(EUCOMM)Hmgu>/Gpcpd1<tm1c(EUCOMM)Hmgu>,Tg(Ucp1-cre)1Evdr/0	involves: C57BL/6J * C57BL/6N * FVB	N	38238601
MGI:7611646	F	MP:0001926	female infertility	Frmd5<em#Yuw>/Frmd5<em#Yuw>	C57BL/6J-Frmd5<em#Yuw>	N	38228891
MGI:7611833	F	MP:0013623	increased femur compact bone thickness	Ezh2<em1Jiaf>/Ezh2<+>	C57BL/6J-Ezh2<em1Jiaf>	N	38015625
MGI:7611833	F	MP:0001260	increased body weight	Ezh2<em1Jiaf>/Ezh2<+>	C57BL/6J-Ezh2<em1Jiaf>	N	38015625
MGI:7611853	M	MP:0002871	albuminuria	Arfip2<tm1d(EUCOMM)Wtsi>/Arfip2<tm1d(EUCOMM)Wtsi>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * CBA	N	38247505
MGI:7611853	M	MP:0030940	impaired autophagy	Arfip2<tm1d(EUCOMM)Wtsi>/Arfip2<tm1d(EUCOMM)Wtsi>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * CBA	N	38247505
MGI:7611853	M	MP:0008873	increased physiological sensitivity to xenobiotic	Arfip2<tm1d(EUCOMM)Wtsi>/Arfip2<tm1d(EUCOMM)Wtsi>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * CBA	N	38247505
MGI:7611853	M	MP:0008059	abnormal podocyte foot process morphology	Arfip2<tm1d(EUCOMM)Wtsi>/Arfip2<tm1d(EUCOMM)Wtsi>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * CBA	N	38247505
MGI:7611853	M	MP:0008060	abnormal podocyte slit diaphragm morphology	Arfip2<tm1d(EUCOMM)Wtsi>/Arfip2<tm1d(EUCOMM)Wtsi>	involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * CBA	N	38247505
MGI:7612031	M	MP:0001547	abnormal lipid level	Creb3<Gt1Mbac>/Creb3<+>	B6NTac.Cg-Creb3<Gt1Mbac>	N	35637262
MGI:7612031	M	MP:0002727	decreased circulating insulin level	Creb3<Gt1Mbac>/Creb3<+>	B6NTac.Cg-Creb3<Gt1Mbac>	N	35637262
MGI:7612031	M	MP:0009356	decreased liver triglyceride level	Creb3<Gt1Mbac>/Creb3<+>	B6NTac.Cg-Creb3<Gt1Mbac>	N	35637262
MGI:7612031	F	MP:0005668	decreased circulating leptin level	Creb3<Gt1Mbac>/Creb3<+>	B6NTac.Cg-Creb3<Gt1Mbac>	N	35637262
MGI:7612031	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Creb3<Gt1Mbac>/Creb3<+>	B6NTac.Cg-Creb3<Gt1Mbac>	N	35637262
MGI:7612031	M	MP:0004777	abnormal phospholipid level	Creb3<Gt1Mbac>/Creb3<+>	B6NTac.Cg-Creb3<Gt1Mbac>	N	35637262
MGI:7612031	F	MP:0005459	decreased percent body fat/body weight	Creb3<Gt1Mbac>/Creb3<+>	B6NTac.Cg-Creb3<Gt1Mbac>	N	35637262
MGI:7612031	F	MP:0031414	decreased skeletal muscle triglyceride level	Creb3<Gt1Mbac>/Creb3<+>	B6NTac.Cg-Creb3<Gt1Mbac>	N	35637262
MGI:7612031	M	MP:0005292	improved glucose tolerance	Creb3<Gt1Mbac>/Creb3<+>	B6NTac.Cg-Creb3<Gt1Mbac>	N	35637262
MGI:7612206	M	MP:0005292	improved glucose tolerance	Armcx3<tm1.1Eso>/Y,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	33807672
MGI:7612206	M	MP:0010025	decreased total body fat amount	Armcx3<tm1.1Eso>/Y,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	33807672
MGI:7612206	M	MP:0005659	decreased susceptibility to diet-induced obesity	Armcx3<tm1.1Eso>/Y,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	33807672
MGI:7612206	M	MP:0011939	increased food intake	Armcx3<tm1.1Eso>/Y,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	33807672
MGI:7612206	M	MP:0003448	abnormal tumor morphology	Armcx3<tm1.1Eso>/Y,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	33807672
MGI:7612206	M	MP:0002891	increased insulin sensitivity	Armcx3<tm1.1Eso>/Y,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	33807672
MGI:7612206	M	MP:0004502	decreased incidence of tumors by chemical induction	Armcx3<tm1.1Eso>/Y,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	33807672
MGI:7612206	M	MP:0002079	increased circulating insulin level	Armcx3<tm1.1Eso>/Y,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	33807672
MGI:7612206	M	MP:0005560	decreased circulating glucose level	Armcx3<tm1.1Eso>/Y,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	33807672
MGI:7612206	M	MP:0002942	decreased circulating alanine transaminase level	Armcx3<tm1.1Eso>/Y,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	33807672
MGI:7612206	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Armcx3<tm1.1Eso>/Y,Ndor1<Tg(UBC-cre/ERT2)1Ejb>/Ndor1<+>	involves: 129S/SvEv * C57BL/6	N	33807672
MGI:7612275	M	MP:0003402	decreased liver weight	Tmem263<em1Gww>/Tmem263<em1Gww>	C57BL/6J-Tmem263<em1Gww>	N	38241182
MGI:7612275	M	MP:0004953	decreased spleen weight	Tmem263<em1Gww>/Tmem263<em1Gww>	C57BL/6J-Tmem263<em1Gww>	N	38241182
MGI:7614306	F	MP:0005389	reproductive system phenotype	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	Y	31712393
MGI:7614306	M	MP:0004901	decreased male germ cell number	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614306	M	MP:0001935	decreased litter size	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614306	M	MP:0001147	small testis	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614306	M	MP:0008280	abnormal male germ cell apoptosis	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614306	M	MP:0002662	abnormal cauda epididymis morphology	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614306	M	MP:0004852	decreased testis weight	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614306	M	MP:0002216	abnormal seminiferous tubule morphology	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614306	M	MP:0001156	abnormal spermatogenesis	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614306	M	MP:0001925	male infertility	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614306	M	MP:0009851	abnormal Sertoli cell phagocytosis	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614306	M	MP:0002784	abnormal Sertoli cell morphology	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614306	M	MP:0014052	increased male germ cell apoptosis	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614306	M	MP:0006428	ectopic Sertoli cells	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614306	M	MP:0002687	oligozoospermia	Xkr8<tm1.2Osa>/Xkr8<tm1.2Osa>	B6.Cg-Xkr8<tm1.2Osa>	N	31712393
MGI:7614555	F	MP:0001364	decreased anxiety-related response	Trhr2<tm1Gemc>/Trhr2<tm1Gemc>	involves: 129S6/SvEvTac	N	19078951
MGI:7614555	F	MP:0003360	abnormal depression-related behavior	Trhr2<tm1Gemc>/Trhr2<tm1Gemc>	involves: 129S6/SvEvTac	N	19078951
MGI:7615074	M	MP:0001405	impaired coordination	Dtna<tm1Jrs>/Dtna<tm1Jrs>	B6;129-Dtna<tm1Jrs>/J	N	37461313
MGI:7615084	F	MP:0006205	embryonic lethality between implantation and somite formation	Mbtps2<em1Sapo>/Mbtps2<em1Sapo>	C57BL/6J-Mbtps2<em1Sapo>	N	37797712
MGI:7615085	M	MP:0006205	embryonic lethality between implantation and somite formation	Mbtps2<em1Sapo>/Y	C57BL/6J-Mbtps2<em1Sapo>	N	37797712
MGI:7615086	F	MP:0020137	decreased bone mineralization	Mbtps2<em1Sapo>/Mbtps2<+>	C57BL/6J-Mbtps2<em1Sapo>	N	37797712
MGI:7615086	F	MP:0030486	abnormal osteocyte canaliculus morphology	Mbtps2<em1Sapo>/Mbtps2<+>	C57BL/6J-Mbtps2<em1Sapo>	N	37797712
MGI:7615086	F	MP:0005378	growth/size/body region phenotype	Mbtps2<em1Sapo>/Mbtps2<+>	C57BL/6J-Mbtps2<em1Sapo>	Y	37797712
MGI:7615086	F	MP:0014025	decreased subchondral bone mineral content	Mbtps2<em1Sapo>/Mbtps2<+>	C57BL/6J-Mbtps2<em1Sapo>	N	37797712
MGI:7615086	F	MP:0006433	abnormal articular cartilage morphology	Mbtps2<em1Sapo>/Mbtps2<+>	C57BL/6J-Mbtps2<em1Sapo>	N	37797712
MGI:7615086	F	MP:0011692	increased chondrocyte number	Mbtps2<em1Sapo>/Mbtps2<+>	C57BL/6J-Mbtps2<em1Sapo>	N	37797712
MGI:7615086	F	MP:0005390	skeleton phenotype	Mbtps2<em1Sapo>/Mbtps2<+>	C57BL/6J-Mbtps2<em1Sapo>	Y	37797712
MGI:7615086	F	MP:0000130	abnormal trabecular bone morphology	Mbtps2<em1Sapo>/Mbtps2<+>	C57BL/6J-Mbtps2<em1Sapo>	N	37797712
MGI:7615087	F	MP:0005390	skeleton phenotype	Mbtps2<em2Sapo>/Mbtps2<+>	involves: C57BL/6J * CBA	Y	37797712
MGI:7615087	F	MP:0030486	abnormal osteocyte canaliculus morphology	Mbtps2<em2Sapo>/Mbtps2<+>	involves: C57BL/6J * CBA	N	37797712
MGI:7615087	F	MP:0006433	abnormal articular cartilage morphology	Mbtps2<em2Sapo>/Mbtps2<+>	involves: C57BL/6J * CBA	N	37797712
MGI:7615087	F	MP:0005378	growth/size/body region phenotype	Mbtps2<em2Sapo>/Mbtps2<+>	involves: C57BL/6J * CBA	Y	37797712
MGI:7615087	F	MP:0006396	decreased long bone epiphyseal plate size	Mbtps2<em2Sapo>/Mbtps2<+>	involves: C57BL/6J * CBA	N	37797712
MGI:7615088	M	MP:0006205	embryonic lethality between implantation and somite formation	Mbtps2<em2Sapo>/Y	involves: C57BL/6J * CBA	N	37797712
MGI:7615089	F	MP:0006205	embryonic lethality between implantation and somite formation	Mbtps2<em2Sapo>/Mbtps2<em2Sapo>	involves: C57BL/6J * CBA	N	37797712
MGI:7615228	M	MP:0010238	increased skeletal muscle weight	Mir92b<em22Gpt>/Mir92b<em22Gpt>	involves: C57BL/6JGpt	N	37985354
MGI:7615228	M	MP:0012107	enhanced exercise endurance	Mir92b<em22Gpt>/Mir92b<em22Gpt>	involves: C57BL/6JGpt	N	37985354
MGI:7615228	M	MP:0000759	abnormal skeletal muscle morphology	Mir92b<em22Gpt>/Mir92b<em22Gpt>	involves: C57BL/6JGpt	N	37985354
MGI:7615228	M	MP:0010401	increased skeletal muscle glycogen level	Mir92b<em22Gpt>/Mir92b<em22Gpt>	involves: C57BL/6JGpt	N	37985354
MGI:7615228	M	MP:0002891	increased insulin sensitivity	Mir92b<em22Gpt>/Mir92b<em22Gpt>	involves: C57BL/6JGpt	N	37985354
MGI:7615228	M	MP:0005292	improved glucose tolerance	Mir92b<em22Gpt>/Mir92b<em22Gpt>	involves: C57BL/6JGpt	N	37985354
MGI:7615228	M	MP:0003960	increased lean body mass	Mir92b<em22Gpt>/Mir92b<em22Gpt>	involves: C57BL/6JGpt	N	37985354
MGI:7615228	M	MP:0014143	decreased body fat mass	Mir92b<em22Gpt>/Mir92b<em22Gpt>	involves: C57BL/6JGpt	N	37985354
MGI:7615228	M	MP:0005369	muscle phenotype	Mir92b<em22Gpt>/Mir92b<em22Gpt>	involves: C57BL/6JGpt	Y	37985354
MGI:7616307	M	MP:0000183	decreased circulating LDL cholesterol level	Rnf130<tm1a(EUCOMM)Wtsi>/Rnf130<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	36876496
MGI:7616307	M	MP:0008469	abnormal protein level	Rnf130<tm1a(EUCOMM)Wtsi>/Rnf130<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	36876496
MGI:7616307	M	MP:0005179	decreased circulating cholesterol level	Rnf130<tm1a(EUCOMM)Wtsi>/Rnf130<tm1a(EUCOMM)Wtsi>	involves: C57BL/6N	N	36876496
MGI:7616310	M	MP:0005376	homeostasis/metabolism phenotype	Rnf130<tm1a(EUCOMM)Wtsi>/Rnf130<+>	involves: C57BL/6N	Y	36876496
MGI:7616737	M	MP:0000062	increased bone mineral density	Pls3<em1Bult>/Y	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7616737	M	MP:0011086	postnatal lethality, incomplete penetrance	Pls3<em1Bult>/Y	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7616737	M	MP:0005388	respiratory system phenotype	Pls3<em1Bult>/Y	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7616737	M	MP:0010770	preweaning lethality	Pls3<em1Bult>/Y	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7616737	M	MP:0002279	abnormal diaphragm morphology	Pls3<em1Bult>/Y	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7616737	M	MP:0013857	abnormal abdominal muscle morphology	Pls3<em1Bult>/Y	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7616737	M	MP:0003924	diaphragmatic hernia	Pls3<em1Bult>/Y	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7616737	M	MP:0000757	herniated abdominal wall	Pls3<em1Bult>/Y	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7616737	M	MP:0000761	thin diaphragm muscle	Pls3<em1Bult>/Y	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7616737	M	MP:0005376	homeostasis/metabolism phenotype	Pls3<em1Bult>/Y	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7616737	M	MP:0011088	neonatal lethality, incomplete penetrance	Pls3<em1Bult>/Y	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7616737	M	MP:0003257	abnormal abdominal wall morphology	Pls3<em1Bult>/Y	C57BL/6J-Pls3<em1Bult>/BultJ	N	37751738
MGI:7616744	M	MP:0000063	decreased bone mineral density	Pls3<em2Bult>/Y	C57BL/6J-Pls3<em2Bult>/BultJ	N	37751738
MGI:7616756	M	MP:0003070	increased vascular permeability	Zfp185<em1Cya>/Y	C57BL/6J-Zfp185<em1Cya>	N	36631535
MGI:7616770	M	MP:0009230	abnormal sperm head morphology	Ccdc157<em1Ymxi>/Ccdc157<em1Ymxi>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616770	M	MP:0008898	abnormal acrosome morphology	Ccdc157<em1Ymxi>/Ccdc157<em1Ymxi>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616770	M	MP:0002675	asthenozoospermia	Ccdc157<em1Ymxi>/Ccdc157<em1Ymxi>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616770	M	MP:0001925	male infertility	Ccdc157<em1Ymxi>/Ccdc157<em1Ymxi>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616770	M	MP:0004910	decreased seminal vesicle weight	Ccdc157<em1Ymxi>/Ccdc157<em1Ymxi>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616770	M	MP:0030980	abnormal acroplaxome morphology	Ccdc157<em1Ymxi>/Ccdc157<em1Ymxi>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616770	M	MP:0002687	oligozoospermia	Ccdc157<em1Ymxi>/Ccdc157<em1Ymxi>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616770	M	MP:0009231	detached acrosome	Ccdc157<em1Ymxi>/Ccdc157<em1Ymxi>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616770	M	MP:0004929	decreased epididymis weight	Ccdc157<em1Ymxi>/Ccdc157<em1Ymxi>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616770	M	MP:0004182	abnormal spermiation	Ccdc157<em1Ymxi>/Ccdc157<em1Ymxi>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616770	F	MP:0001385	pup cannibalization	Ccdc157<em1Ymxi>/Ccdc157<em1Ymxi>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616770	M	MP:0009234	absent sperm head	Ccdc157<em1Ymxi>/Ccdc157<em1Ymxi>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616770	M	MP:0009232	abnormal sperm nucleus morphology	Ccdc157<em1Ymxi>/Ccdc157<em1Ymxi>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616777	M	MP:0002675	asthenozoospermia	Ccdc157<em1Ymxi>/Ccdc157<+>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616777	F	MP:0001385	pup cannibalization	Ccdc157<em1Ymxi>/Ccdc157<+>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616777	M	MP:0008975	delayed male fertility	Ccdc157<em1Ymxi>/Ccdc157<+>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616777	M	MP:0009230	abnormal sperm head morphology	Ccdc157<em1Ymxi>/Ccdc157<+>	C57BL/6-Ccdc157<em1Ymxi>	N	38509755
MGI:7616935	F	MP:0009419	skeletal muscle fibrosis	Mustn1<tm1d(EUCOMM)Wtsi>/Mustn1<tm1d(EUCOMM)Wtsi>	involves: C57BL/6N * SJL	N	38458566
MGI:7616935	F	MP:0005165	increased susceptibility to injury	Mustn1<tm1d(EUCOMM)Wtsi>/Mustn1<tm1d(EUCOMM)Wtsi>	involves: C57BL/6N * SJL	N	38458566
MGI:7616987	M	MP:0005583	decreased renin activity	Or51e1<tm1Jplu>/Or51e1<tm1Jplu>	C57BL/6N-Or51e1<tm1Jplu>/J	N	38507492
MGI:7616987	F	MP:0003025	increased vasoconstriction	Or51e1<tm1Jplu>/Or51e1<tm1Jplu>	C57BL/6N-Or51e1<tm1Jplu>/J	N	38507492
MGI:7616987	F	MP:0000230	abnormal systemic arterial blood pressure	Or51e1<tm1Jplu>/Or51e1<tm1Jplu>	C57BL/6N-Or51e1<tm1Jplu>/J	N	38507492
MGI:7616987	M	MP:0005590	increased vasodilation	Or51e1<tm1Jplu>/Or51e1<tm1Jplu>	C57BL/6N-Or51e1<tm1Jplu>/J	N	38507492
MGI:7616987	F	MP:0004875	increased mean systemic arterial blood pressure	Or51e1<tm1Jplu>/Or51e1<tm1Jplu>	C57BL/6N-Or51e1<tm1Jplu>/J	N	38507492
MGI:7616987	M	MP:0006263	decreased systemic arterial diastolic blood pressure	Or51e1<tm1Jplu>/Or51e1<tm1Jplu>	C57BL/6N-Or51e1<tm1Jplu>/J	N	38507492
MGI:7616987	M	MP:0003026	decreased vasoconstriction	Or51e1<tm1Jplu>/Or51e1<tm1Jplu>	C57BL/6N-Or51e1<tm1Jplu>/J	N	38507492
MGI:7616987	F	MP:0005595	abnormal vascular smooth muscle physiology	Or51e1<tm1Jplu>/Or51e1<tm1Jplu>	C57BL/6N-Or51e1<tm1Jplu>/J	N	38507492
MGI:7616987	F	MP:0031391	increased locomotor activity	Or51e1<tm1Jplu>/Or51e1<tm1Jplu>	C57BL/6N-Or51e1<tm1Jplu>/J	N	38507492
MGI:7618283	M	MP:0020596	decreased cerebral cortex total cell area	Tubg1<tm1.1Ics>/Tubg1<+>	involves: C57BL/6N	N	31086189
MGI:7618283	M	MP:0000433	microcephaly	Tubg1<tm1.1Ics>/Tubg1<+>	involves: C57BL/6N	N	31086189
MGI:7618283	M	MP:0000852	small cerebellum	Tubg1<tm1.1Ics>/Tubg1<+>	involves: C57BL/6N	N	31086189
MGI:7618283	M	MP:0008263	abnormal hippocampus CA1 region morphology	Tubg1<tm1.1Ics>/Tubg1<+>	involves: C57BL/6N	N	31086189
MGI:7618283	M	MP:0006254	thin cerebral cortex	Tubg1<tm1.1Ics>/Tubg1<+>	involves: C57BL/6N	N	31086189
MGI:7618283	M	MP:0020570	decreased premotor cortex size	Tubg1<tm1.1Ics>/Tubg1<+>	involves: C57BL/6N	N	31086189
MGI:7618283	M	MP:0003631	nervous system phenotype	Tubg1<tm1.1Ics>/Tubg1<+>	involves: C57BL/6N	Y	31086189
MGI:7618283	M	MP:0000774	decreased brain size	Tubg1<tm1.1Ics>/Tubg1<+>	involves: C57BL/6N	N	31086189
MGI:7618283	M	MP:0008026	abnormal brain white matter morphology	Tubg1<tm1.1Ics>/Tubg1<+>	involves: C57BL/6N	N	31086189
MGI:7618283	M	MP:0008225	abnormal anterior commissure morphology	Tubg1<tm1.1Ics>/Tubg1<+>	involves: C57BL/6N	N	31086189
MGI:7618283	M	MP:0000790	abnormal stratification in cerebral cortex	Tubg1<tm1.1Ics>/Tubg1<+>	involves: C57BL/6N	N	31086189
MGI:7618532	M	MP:0002640	reticulocytosis	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	F	MP:0001402	decreased locomotor activity	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	M	MP:0009292	increased inguinal fat pad weight	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	F	MP:0002608	increased hematocrit	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	F	MP:0005289	increased oxygen consumption	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	M	MP:0010053	decreased grip strength	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	M	MP:0005331	insulin resistance	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	M	MP:0014142	increased body fat mass	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	F	MP:0011957	decreased compensatory feeding amount	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	F	MP:0005178	increased circulating cholesterol level	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	M	MP:0005016	decreased lymphocyte cell number	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	F	MP:0002575	increased circulating ketone body level	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	F	MP:0004889	increased energy expenditure	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	F	MP:0005564	increased hemoglobin content	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618532	M	MP:0000221	decreased leukocyte cell number	C1ql4<tm1Lex>/C1ql4<tm1Lex>	B6.129S5-C1ql4<tm1Lex>	N	35579659
MGI:7618843	M	MP:0000272	abnormal aorta morphology	Thsd4<tm1.2Lysa>/Thsd4<+>	involves: C57BL/6	N	32855533
MGI:7618843	M	MP:0009865	abnormal aorta smooth muscle morphology	Thsd4<tm1.2Lysa>/Thsd4<+>	involves: C57BL/6	N	32855533
MGI:7618843	M	MP:0010575	aortic arch dilation	Thsd4<tm1.2Lysa>/Thsd4<+>	involves: C57BL/6	N	32855533
MGI:7618843	M	MP:0010574	dilated aorta	Thsd4<tm1.2Lysa>/Thsd4<+>	involves: C57BL/6	N	32855533
MGI:7618843	M	MP:0010470	dilated ascending aorta	Thsd4<tm1.2Lysa>/Thsd4<+>	involves: C57BL/6	N	32855533
MGI:7618843	M	MP:0010473	descending aorta dilation	Thsd4<tm1.2Lysa>/Thsd4<+>	involves: C57BL/6	N	32855533
MGI:7618843	M	MP:0010482	abnormal aortic sinus morphology	Thsd4<tm1.2Lysa>/Thsd4<+>	involves: C57BL/6	N	32855533
MGI:7619086	F	MP:0003845	abnormal decidualization	Greb1<em1Rkom>/Greb1<em1Rkom>	C57BL/6NJ-Greb1<em1Rkom>	N	38431630
MGI:7619086	F	MP:0009662	abnormal uterine receptivity	Greb1<em1Rkom>/Greb1<em1Rkom>	C57BL/6NJ-Greb1<em1Rkom>	N	38431630
MGI:7619086	F	MP:0001935	decreased litter size	Greb1<em1Rkom>/Greb1<em1Rkom>	C57BL/6NJ-Greb1<em1Rkom>	N	38431630
MGI:7619086	F	MP:0009663	abnormal uterine-embryonic axis	Greb1<em1Rkom>/Greb1<em1Rkom>	C57BL/6NJ-Greb1<em1Rkom>	N	38431630
MGI:7619086	F	MP:0009664	abnormal luminal closure	Greb1<em1Rkom>/Greb1<em1Rkom>	C57BL/6NJ-Greb1<em1Rkom>	N	38431630
MGI:7619086	F	MP:0001729	impaired embryo implantation	Greb1<em1Rkom>/Greb1<em1Rkom>	C57BL/6NJ-Greb1<em1Rkom>	N	38431630
MGI:7619086	F	MP:0001923	reduced female fertility	Greb1<em1Rkom>/Greb1<em1Rkom>	C57BL/6NJ-Greb1<em1Rkom>	N	38431630
MGI:7619086	F	MP:0005671	abnormal response to transplant	Greb1<em1Rkom>/Greb1<em1Rkom>	C57BL/6NJ-Greb1<em1Rkom>	N	38431630
MGI:7619846	M	MP:0002675	asthenozoospermia	Iqch<em2Alfon>/Iqch<em2Alfon>	involves: C57BL/6 * CBA	N	36975404
MGI:7619846	M	MP:0001147	small testis	Iqch<em2Alfon>/Iqch<em2Alfon>	involves: C57BL/6 * CBA	N	36975404
MGI:7619846	M	MP:0009831	abnormal sperm midpiece morphology	Iqch<em2Alfon>/Iqch<em2Alfon>	involves: C57BL/6 * CBA	N	36975404
MGI:7619846	M	MP:0008898	abnormal acrosome morphology	Iqch<em2Alfon>/Iqch<em2Alfon>	involves: C57BL/6 * CBA	N	36975404
MGI:7619846	M	MP:0001925	male infertility	Iqch<em2Alfon>/Iqch<em2Alfon>	involves: C57BL/6 * CBA	N	36975404
MGI:7619846	M	MP:0008892	abnormal sperm flagellum morphology	Iqch<em2Alfon>/Iqch<em2Alfon>	involves: C57BL/6 * CBA	N	36975404
MGI:7619846	M	MP:0009230	abnormal sperm head morphology	Iqch<em2Alfon>/Iqch<em2Alfon>	involves: C57BL/6 * CBA	N	36975404
MGI:7619846	M	MP:0004543	abnormal sperm physiology	Iqch<em2Alfon>/Iqch<em2Alfon>	involves: C57BL/6 * CBA	N	36975404
MGI:7619846	M	MP:0002216	abnormal seminiferous tubule morphology	Iqch<em2Alfon>/Iqch<em2Alfon>	involves: C57BL/6 * CBA	N	36975404
MGI:7619846	M	MP:0005578	teratozoospermia	Iqch<em2Alfon>/Iqch<em2Alfon>	involves: C57BL/6 * CBA	N	36975404
MGI:7619846	M	MP:0002687	oligozoospermia	Iqch<em2Alfon>/Iqch<em2Alfon>	involves: C57BL/6 * CBA	N	36975404
MGI:7619909	F	MP:0002968	increased circulating alkaline phosphatase level	Rogdi<tm1.2Ics>/Rogdi<tm1.2Ics>	involves: C57BL/6N	N	38172607
MGI:7619909	M	MP:0000195	decreased circulating calcium level	Rogdi<tm1.2Ics>/Rogdi<tm1.2Ics>	involves: C57BL/6N	N	38172607
MGI:7619909	F	MP:0010053	decreased grip strength	Rogdi<tm1.2Ics>/Rogdi<tm1.2Ics>	involves: C57BL/6N	N	38172607
MGI:7619956	M	MP:0001552	increased circulating triglyceride level	Aldoc<tm1.1(KOMP)Vlcg>/Aldoc<tm1.1(KOMP)Vlcg>	C57BL/6N-Aldoc<tm1.1(KOMP)Vlcg>	N	38417553
MGI:7619956	F	MP:0002644	decreased circulating triglyceride level	Aldoc<tm1.1(KOMP)Vlcg>/Aldoc<tm1.1(KOMP)Vlcg>	C57BL/6N-Aldoc<tm1.1(KOMP)Vlcg>	N	38417553
MGI:7619957	M	MP:0001262	decreased body weight	Aldoc<tm1.1(KOMP)Vlcg>/Aldoc<tm1.1(KOMP)Vlcg>,Ldlr<tm1Her>/Ldlr<tm1Her>	involves: 129S7/SvEvBrd * C57BL/6J * C57BL/6N	N	38417553
MGI:7619957	M	MP:0002644	decreased circulating triglyceride level	Aldoc<tm1.1(KOMP)Vlcg>/Aldoc<tm1.1(KOMP)Vlcg>,Ldlr<tm1Her>/Ldlr<tm1Her>	involves: 129S7/SvEvBrd * C57BL/6J * C57BL/6N	N	38417553
MGI:7619957	M	MP:0003402	decreased liver weight	Aldoc<tm1.1(KOMP)Vlcg>/Aldoc<tm1.1(KOMP)Vlcg>,Ldlr<tm1Her>/Ldlr<tm1Her>	involves: 129S7/SvEvBrd * C57BL/6J * C57BL/6N	N	38417553
MGI:7620017	F	MP:0001926	female infertility	Rtcb<tm1Hyfn>/Rtcb<tm1Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6J	N	36178098
MGI:7620017	F	MP:0001127	small ovary	Rtcb<tm1Hyfn>/Rtcb<tm1Hyfn>,Tg(Gdf9-icre)5092Coo/0	involves: C57BL/6J	N	36178098
MGI:7620431	M	MP:0014117	increased pancreatic beta cell apoptosis	Ier3ip1<tm1Arvn>/Ier3ip1<tm1Arvn>,Tg(Ins1-cre/ERT)1Lphi/0	involves: 129S4/SvJaeSor * C57BL/6J * CD-1	N	36322741
MGI:7620431	M	MP:0001559	hyperglycemia	Ier3ip1<tm1Arvn>/Ier3ip1<tm1Arvn>,Tg(Ins1-cre/ERT)1Lphi/0	involves: 129S4/SvJaeSor * C57BL/6J * CD-1	N	36322741
MGI:7620431	M	MP:0005217	abnormal pancreatic beta cell morphology	Ier3ip1<tm1Arvn>/Ier3ip1<tm1Arvn>,Tg(Ins1-cre/ERT)1Lphi/0	involves: 129S4/SvJaeSor * C57BL/6J * CD-1	N	36322741
MGI:7620431	M	MP:0003059	decreased insulin secretion	Ier3ip1<tm1Arvn>/Ier3ip1<tm1Arvn>,Tg(Ins1-cre/ERT)1Lphi/0	involves: 129S4/SvJaeSor * C57BL/6J * CD-1	N	36322741
MGI:7620431	M	MP:0002727	decreased circulating insulin level	Ier3ip1<tm1Arvn>/Ier3ip1<tm1Arvn>,Tg(Ins1-cre/ERT)1Lphi/0	involves: 129S4/SvJaeSor * C57BL/6J * CD-1	N	36322741
MGI:7620431	M	MP:0009175	abnormal pancreatic beta cell differentiation	Ier3ip1<tm1Arvn>/Ier3ip1<tm1Arvn>,Tg(Ins1-cre/ERT)1Lphi/0	involves: 129S4/SvJaeSor * C57BL/6J * CD-1	N	36322741
MGI:7620431	M	MP:0011820	decreased pancreatic beta cell proliferation	Ier3ip1<tm1Arvn>/Ier3ip1<tm1Arvn>,Tg(Ins1-cre/ERT)1Lphi/0	involves: 129S4/SvJaeSor * C57BL/6J * CD-1	N	36322741
MGI:7620431	M	MP:0005293	impaired glucose tolerance	Ier3ip1<tm1Arvn>/Ier3ip1<tm1Arvn>,Tg(Ins1-cre/ERT)1Lphi/0	involves: 129S4/SvJaeSor * C57BL/6J * CD-1	N	36322741
MGI:7620431	M	MP:0002078	abnormal glucose homeostasis	Ier3ip1<tm1Arvn>/Ier3ip1<tm1Arvn>,Tg(Ins1-cre/ERT)1Lphi/0	involves: 129S4/SvJaeSor * C57BL/6J * CD-1	N	36322741
MGI:7621197	F	MP:0008779	abnormal maternal behavior	Gnb1<em1Dgold>/Gnb1<+>	C57BL/6NJ-Gnb1<em1Dgold>	N	37275776
MGI:7621248	F	MP:0010767	abnormal female meiosis I arrest	Ube2s<tm1.1Smoc>/Ube2s<tm1.1Smoc>	Not Specified	N	38546043
MGI:7621248	F	MP:0005389	reproductive system phenotype	Ube2s<tm1.1Smoc>/Ube2s<tm1.1Smoc>	Not Specified	Y	38546043
MGI:7621248	F	MP:0005168	abnormal female meiosis	Ube2s<tm1.1Smoc>/Ube2s<tm1.1Smoc>	Not Specified	N	38546043
MGI:7621248	F	MP:0001926	female infertility	Ube2s<tm1.1Smoc>/Ube2s<tm1.1Smoc>	Not Specified	N	38546043
MGI:7621295	M	MP:0005159	azoospermia	Cpsf6<em1Bcgen>/Cpsf6<+>	Not Specified	N	38416782
MGI:7621403	M	MP:0005669	increased circulating leptin level	Xrn1<em1Tya>/Xrn1<em1Tya>,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6N * FVB/N	N	34646989
MGI:7621403	M	MP:0001392	abnormal locomotor behavior	Xrn1<em1Tya>/Xrn1<em1Tya>,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6N * FVB/N	N	34646989
MGI:7621403	M	MP:0010378	increased respiratory quotient	Xrn1<em1Tya>/Xrn1<em1Tya>,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6N * FVB/N	N	34646989
MGI:7621403	M	MP:0013245	abnormal lipid metabolism	Xrn1<em1Tya>/Xrn1<em1Tya>,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6N * FVB/N	N	34646989
MGI:7621403	M	MP:0002079	increased circulating insulin level	Xrn1<em1Tya>/Xrn1<em1Tya>,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6N * FVB/N	N	34646989
MGI:7621403	M	MP:0001262	decreased body weight	Xrn1<em1Tya>/Xrn1<em1Tya>,Tg(Camk2a-cre)2Gsc/0	involves: C57BL/6N * FVB/N	N	34646989
MGI:7621581	M	MP:0002942	decreased circulating alanine transaminase level	Sox9<em1(cre/ERT2)Smoc>/Sox9<+>,Tnfsf18<em1Pwan>/Tnfsf18<em1Pwan>	involves: C57BL/6J	N	38321001
MGI:7621581	M	MP:0005164	abnormal response to injury	Sox9<em1(cre/ERT2)Smoc>/Sox9<+>,Tnfsf18<em1Pwan>/Tnfsf18<em1Pwan>	involves: C57BL/6J	N	38321001
MGI:7621581	M	MP:0005632	decreased circulating aspartate transaminase level	Sox9<em1(cre/ERT2)Smoc>/Sox9<+>,Tnfsf18<em1Pwan>/Tnfsf18<em1Pwan>	involves: C57BL/6J	N	38321001
MGI:7621581	M	MP:0012243	decreased hepatoblast number	Sox9<em1(cre/ERT2)Smoc>/Sox9<+>,Tnfsf18<em1Pwan>/Tnfsf18<em1Pwan>	involves: C57BL/6J	N	38321001
MGI:7621581	M	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Sox9<em1(cre/ERT2)Smoc>/Sox9<+>,Tnfsf18<em1Pwan>/Tnfsf18<em1Pwan>	involves: C57BL/6J	N	38321001
MGI:7621581	M	MP:0001876	decreased inflammatory response	Sox9<em1(cre/ERT2)Smoc>/Sox9<+>,Tnfsf18<em1Pwan>/Tnfsf18<em1Pwan>	involves: C57BL/6J	N	38321001
MGI:7621581	M	MP:0001828	abnormal T cell activation	Sox9<em1(cre/ERT2)Smoc>/Sox9<+>,Tnfsf18<em1Pwan>/Tnfsf18<em1Pwan>	involves: C57BL/6J	N	38321001
MGI:7621646	M	MP:0009454	impaired contextual conditioning behavior	Chrna2<tm1.1Slot>/Chrna2<tm1.1Slot>	involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6J	N	28507032
MGI:7621646	M	MP:0003631	nervous system phenotype	Chrna2<tm1.1Slot>/Chrna2<tm1.1Slot>	involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6J	Y	28507032
MGI:7621646	M	MP:0005380	embryo phenotype	Chrna2<tm1.1Slot>/Chrna2<tm1.1Slot>	involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6J	Y	28507032
MGI:7621646	M	MP:0003008	enhanced long-term potentiation	Chrna2<tm1.1Slot>/Chrna2<tm1.1Slot>	involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6J	N	28507032
MGI:7621646	M	MP:0005378	growth/size/body region phenotype	Chrna2<tm1.1Slot>/Chrna2<tm1.1Slot>	involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6J	Y	28507032
MGI:7621646	M	MP:0002574	increased vertical activity	Chrna2<tm1.1Slot>/Chrna2<tm1.1Slot>	involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6J	N	28507032
MGI:7621646	M	MP:0031391	increased locomotor activity	Chrna2<tm1.1Slot>/Chrna2<tm1.1Slot>	involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6J	N	28507032
MGI:7621646	M	MP:0005386	behavior/neurological phenotype	Chrna2<tm1.1Slot>/Chrna2<tm1.1Slot>	involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6J	Y	28507032
MGI:7622051	M	MP:0001399	hyperactivity	Npvf<tm1.1Ubu>/Npvf<tm1.1Ubu>,Tg(Nes-cre)1Nogu/0	involves: C57BL/6	N	36355189
MGI:7622051	M	MP:0031392	hypoactivity	Npvf<tm1.1Ubu>/Npvf<tm1.1Ubu>,Tg(Nes-cre)1Nogu/0	involves: C57BL/6	N	36355189
MGI:7622051	M	MP:0001364	decreased anxiety-related response	Npvf<tm1.1Ubu>/Npvf<tm1.1Ubu>,Tg(Nes-cre)1Nogu/0	involves: C57BL/6	N	36355189
MGI:7622051	M	MP:0001973	increased thermal nociceptive threshold	Npvf<tm1.1Ubu>/Npvf<tm1.1Ubu>,Tg(Nes-cre)1Nogu/0	involves: C57BL/6	N	36355189
MGI:7622051	M	MP:0005386	behavior/neurological phenotype	Npvf<tm1.1Ubu>/Npvf<tm1.1Ubu>,Tg(Nes-cre)1Nogu/0	involves: C57BL/6	Y	36355189
MGI:7623147	M	MP:0001260	increased body weight	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623147	M	MP:0002833	increased heart weight	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623147	M	MP:0011692	increased chondrocyte number	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623147	M	MP:0009780	abnormal chondrocyte physiology	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623147	M	MP:0001264	increased body size	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623147	M	MP:0002981	increased liver weight	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623147	M	MP:0004357	long tibia	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623147	M	MP:0002176	increased brain weight	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623147	M	MP:0014100	increased chondrocyte proliferation	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623147	M	MP:0005630	increased lung weight	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623147	M	MP:0006398	increased long bone epiphyseal plate size	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623147	M	MP:0004952	increased spleen weight	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623147	M	MP:0003917	increased kidney weight	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623147	M	MP:0001257	increased body length	Spin4<em1Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623148	F	MP:0001260	increased body weight	Spin4<em1Jbn>/Spin4<+>	involves: C57BL/6J	N	36927955
MGI:7623149	F	MP:0001260	increased body weight	Spin4<em1Jbn>/Spin4<em1Jbn>	involves: C57BL/6J	N	36927955
MGI:7623150	M	MP:0003917	increased kidney weight	Spin4<em2Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623150	M	MP:0014100	increased chondrocyte proliferation	Spin4<em2Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623150	M	MP:0001264	increased body size	Spin4<em2Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623150	M	MP:0004357	long tibia	Spin4<em2Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623150	M	MP:0004952	increased spleen weight	Spin4<em2Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623150	M	MP:0006398	increased long bone epiphyseal plate size	Spin4<em2Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623150	M	MP:0011692	increased chondrocyte number	Spin4<em2Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623150	M	MP:0002833	increased heart weight	Spin4<em2Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623150	M	MP:0001257	increased body length	Spin4<em2Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623150	M	MP:0002176	increased brain weight	Spin4<em2Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623150	M	MP:0002981	increased liver weight	Spin4<em2Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623150	M	MP:0001260	increased body weight	Spin4<em2Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623150	M	MP:0005630	increased lung weight	Spin4<em2Jbn>/Y	involves: C57BL/6J	N	36927955
MGI:7623151	F	MP:0001260	increased body weight	Spin4<em2Jbn>/Spin4<+>	involves: C57BL/6J	N	36927955
MGI:7623152	F	MP:0001260	increased body weight	Spin4<em2Jbn>/Spin4<em2Jbn>	involves: C57BL/6J	N	36927955
MGI:7623214	M	MP:0020354	increased endoplasmic reticulum stress	Stim1<tm3Ics>/Stim1<+>	involves: C57BL/6N	N	34359900
MGI:7623214	F	MP:0011585	decreased alkaline phosphatase activity	Stim1<tm3Ics>/Stim1<+>	involves: C57BL/6N	N	30576443
MGI:7623214	M	MP:0031318	enhanced skeletal muscle regeneration	Stim1<tm3Ics>/Stim1<+>	involves: C57BL/6N	N	34359900
MGI:7623214	M	MP:0020240	increased skeletal muscle cell apoptosis	Stim1<tm3Ics>/Stim1<+>	involves: C57BL/6N	N	34359900
MGI:7623214	M	MP:0010959	abnormal oxidative phosphorylation	Stim1<tm3Ics>/Stim1<+>	involves: C57BL/6N	N	34359900
MGI:7623214	M	MP:0002106	abnormal muscle physiology	Stim1<tm3Ics>/Stim1<+>	involves: C57BL/6N	N	34359900
MGI:7623214	M	MP:0011629	decreased mitochondrial number	Stim1<tm3Ics>/Stim1<+>	involves: C57BL/6N	N	34359900
MGI:7623214	M	MP:0005292	improved glucose tolerance	Stim1<tm3Ics>/Stim1<+>	involves: C57BL/6N	N	30576443
MGI:7623214	M	MP:0000747	muscle weakness	Stim1<tm3Ics>/Stim1<+>	involves: C57BL/6N	N	30576443
MGI:7623214	M	MP:0003084	abnormal skeletal muscle fiber morphology	Stim1<tm3Ics>/Stim1<+>	involves: C57BL/6N	N	34359900
MGI:7623600	M	MP:0002807	abnormal eye blink conditioning behavior	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	N	35121636
MGI:7623600	M	MP:0002797	increased thigmotaxis	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	N	35121636
MGI:7623600	M	MP:0005386	behavior/neurological phenotype	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	Y	35121636
MGI:7623600	M	MP:0012307	impaired spatial learning	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	N	35121636
MGI:7623600	M	MP:0001488	increased startle reflex	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	N	35121636
MGI:7623600	M	MP:0001399	hyperactivity	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	N	35121636
MGI:7623600	M	MP:0009747	impaired behavioral response to xenobiotic	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	N	35121636
MGI:7623600	M	MP:0001363	increased anxiety-related response	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	N	35121636
MGI:7623600	M	MP:0009746	enhanced behavioral response to xenobiotic	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	N	35121636
MGI:7623600	M	MP:0002906	increased susceptibility to pharmacologically induced seizures	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	N	35121636
MGI:7623600	M	MP:0009745	abnormal behavioral response to xenobiotic	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	N	35121636
MGI:7623600	M	MP:0003631	nervous system phenotype	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	Y	35121636
MGI:7623600	M	MP:0002574	increased vertical activity	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	N	35121636
MGI:7623600	M	MP:0021111	decreased social investigation	Sipa1l1<tm1Taki>/Sipa1l1<tm1Taki>	B6.Cg-Sipa1l1<tm1Taki>/Taki	N	35121636
MGI:7623670	M	MP:0004777	abnormal phospholipid level	Mtarc1<tm1.1Vlcg>/Mtarc1<tm1.1Vlcg>	involves: 129S6/SvEvTac * C57BL/6NTac	N	38437227
MGI:7623670	M	MP:0000598	abnormal liver morphology	Mtarc1<tm1.1Vlcg>/Mtarc1<tm1.1Vlcg>	involves: 129S6/SvEvTac * C57BL/6NTac	N	38437227
MGI:7623670	M	MP:0009356	decreased liver triglyceride level	Mtarc1<tm1.1Vlcg>/Mtarc1<tm1.1Vlcg>	involves: 129S6/SvEvTac * C57BL/6NTac	N	38437227
MGI:7623670	M	MP:0002942	decreased circulating alanine transaminase level	Mtarc1<tm1.1Vlcg>/Mtarc1<tm1.1Vlcg>	involves: 129S6/SvEvTac * C57BL/6NTac	N	38437227
MGI:7623676	F	MP:0001262	decreased body weight	Mtarc2<tm1.1Vlcg>/Mtarc2<tm1.1Vlcg>	involves: C57BL/6NTac	N	38437227
MGI:7623676	F	MP:0014143	decreased body fat mass	Mtarc2<tm1.1Vlcg>/Mtarc2<tm1.1Vlcg>	involves: C57BL/6NTac	N	38437227
MGI:7624256	M	MP:0004215	abnormal myocardial fiber physiology	Calm1<em1Allg>/Calm1<+>	C57BL/6J-Calm1<em1Allg>	N	37589122
MGI:7624256	M	MP:0009732	ventricular premature beat	Calm1<em1Allg>/Calm1<+>	C57BL/6J-Calm1<em1Allg>	N	37589122
MGI:7624256	M	MP:0004085	abnormal heartbeat	Calm1<em1Allg>/Calm1<+>	C57BL/6J-Calm1<em1Allg>	N	37589122
MGI:7624256	M	MP:0001265	decreased body size	Calm1<em1Allg>/Calm1<+>	C57BL/6J-Calm1<em1Allg>	N	37589122
MGI:7624256	M	MP:0008950	ventricular tachycardia	Calm1<em1Allg>/Calm1<+>	C57BL/6J-Calm1<em1Allg>	N	37589122
MGI:7624256	M	MP:0011101	prenatal lethality, incomplete penetrance	Calm1<em1Allg>/Calm1<+>	C57BL/6J-Calm1<em1Allg>	N	37589122
MGI:7624256	M	MP:0010392	prolonged QRS complex duration	Calm1<em1Allg>/Calm1<+>	C57BL/6J-Calm1<em1Allg>	N	37589122
MGI:7624256	M	MP:0003233	prolonged QT interval	Calm1<em1Allg>/Calm1<+>	C57BL/6J-Calm1<em1Allg>	N	37589122
MGI:7624260	M	MP:0004215	abnormal myocardial fiber physiology	Calm2<em1Allg>/Calm2<+>	C57BL/6J-Calm2<em1Allg>	N	37589122
MGI:7624328	M	MP:0020913	increased susceptibility to Riboviria infection	Zc3h7ait<em1Caox>/Zc3h7ait<em1Caox>	C57BL/6J-Zc3h7ait<em1Caox>	N	31036902
MGI:7624328	M	MP:0005387	immune system phenotype	Zc3h7ait<em1Caox>/Zc3h7ait<em1Caox>	C57BL/6J-Zc3h7ait<em1Caox>	Y	31036902
MGI:7624328	M	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality	Zc3h7ait<em1Caox>/Zc3h7ait<em1Caox>	C57BL/6J-Zc3h7ait<em1Caox>	N	31036902
MGI:7624328	M	MP:0011075	abnormal macrophage activation involved in immune response	Zc3h7ait<em1Caox>/Zc3h7ait<em1Caox>	C57BL/6J-Zc3h7ait<em1Caox>	N	31036902
MGI:7624328	M	MP:0008565	decreased interferon-beta secretion	Zc3h7ait<em1Caox>/Zc3h7ait<em1Caox>	C57BL/6J-Zc3h7ait<em1Caox>	N	31036902
MGI:7624328	M	MP:0008576	decreased circulating interferon-beta level	Zc3h7ait<em1Caox>/Zc3h7ait<em1Caox>	C57BL/6J-Zc3h7ait<em1Caox>	N	31036902
MGI:7624328	M	MP:0008555	abnormal interferon secretion	Zc3h7ait<em1Caox>/Zc3h7ait<em1Caox>	C57BL/6J-Zc3h7ait<em1Caox>	N	31036902
MGI:7624328	M	MP:0008574	decreased circulating interferon-alpha level	Zc3h7ait<em1Caox>/Zc3h7ait<em1Caox>	C57BL/6J-Zc3h7ait<em1Caox>	N	31036902
MGI:7624328	M	MP:0008563	decreased interferon-alpha secretion	Zc3h7ait<em1Caox>/Zc3h7ait<em1Caox>	C57BL/6J-Zc3h7ait<em1Caox>	N	31036902
MGI:7624328	M	MP:0008597	decreased circulating interleukin-6 level	Zc3h7ait<em1Caox>/Zc3h7ait<em1Caox>	C57BL/6J-Zc3h7ait<em1Caox>	N	31036902
MGI:7624328	M	MP:0008706	decreased interleukin-6 secretion	Zc3h7ait<em1Caox>/Zc3h7ait<em1Caox>	C57BL/6J-Zc3h7ait<em1Caox>	N	31036902
MGI:7624352	M	MP:0005389	reproductive system phenotype	Magea10<em1Prp> Magea4<em1Prp>/Y	involves: C57BL/6	N	31149633
MGI:7624352	M	MP:0005376	homeostasis/metabolism phenotype	Magea10<em1Prp> Magea4<em1Prp>/Y	involves: C57BL/6	Y	31149633
MGI:7624353	M	MP:0002216	abnormal seminiferous tubule morphology	Del(XMagea6-Magea1)1Prp Magea10<em1Prp> Magea4<em1Prp>/Y	involves: C57BL/6	N	31149633
MGI:7624353	M	MP:0008873	increased physiological sensitivity to xenobiotic	Del(XMagea6-Magea1)1Prp Magea10<em1Prp> Magea4<em1Prp>/Y	involves: C57BL/6	N	31149633
MGI:7624353	M	MP:0005389	reproductive system phenotype	Del(XMagea6-Magea1)1Prp Magea10<em1Prp> Magea4<em1Prp>/Y	involves: C57BL/6	N	31149633
MGI:7624353	M	MP:0001922	reduced male fertility	Del(XMagea6-Magea1)1Prp Magea10<em1Prp> Magea4<em1Prp>/Y	involves: C57BL/6	N	31149633
MGI:7624353	M	MP:0004852	decreased testis weight	Del(XMagea6-Magea1)1Prp Magea10<em1Prp> Magea4<em1Prp>/Y	involves: C57BL/6	N	31149633
MGI:7624356	M	MP:0004852	decreased testis weight	Del(XMagea6-Magea1)1Prp/Y	involves: C57BL/6	N	31149633
MGI:7624356	M	MP:0008873	increased physiological sensitivity to xenobiotic	Del(XMagea6-Magea1)1Prp/Y	involves: C57BL/6	N	31149633
MGI:7624356	M	MP:0002216	abnormal seminiferous tubule morphology	Del(XMagea6-Magea1)1Prp/Y	involves: C57BL/6	N	31149633
MGI:7624356	M	MP:0001922	reduced male fertility	Del(XMagea6-Magea1)1Prp/Y	involves: C57BL/6	N	31149633
MGI:7624356	M	MP:0005389	reproductive system phenotype	Del(XMagea6-Magea1)1Prp/Y	involves: C57BL/6	Y	31149633
MGI:7624356	M	MP:0002687	oligozoospermia	Del(XMagea6-Magea1)1Prp/Y	involves: C57BL/6	N	31149633
MGI:7627155	M	MP:0021111	decreased social investigation	Taok1<em1Bcgen>/Taok1<+>	C57BL/6N-Taok1<em1Bcgen>	N	37656623
MGI:7627155	M	MP:0001399	hyperactivity	Taok1<em1Bcgen>/Taok1<+>	C57BL/6N-Taok1<em1Bcgen>	N	37656623
MGI:7627167	M	MP:0001409	increased stereotypic behavior	Taok1<em1Cya>/Taok1<em1Cya>,Tg(Slc17a8-icre)1Edw/0	involves: C57BL/6J * FVB/N	N	37656623
MGI:7627167	M	MP:0001441	increased grooming behavior	Taok1<em1Cya>/Taok1<em1Cya>,Tg(Slc17a8-icre)1Edw/0	involves: C57BL/6J * FVB/N	N	37656623
MGI:7627167	M	MP:0021111	decreased social investigation	Taok1<em1Cya>/Taok1<em1Cya>,Tg(Slc17a8-icre)1Edw/0	involves: C57BL/6J * FVB/N	N	37656623
MGI:7627365	M	MP:0012289	abnormal non-rapid eye movement sleep pattern	Tfap2b<em1Sleep>/Tfap2b<+>	C57BL/6J-Tfap2b<em1Sleep>	N	32878901
MGI:7627365	M	MP:0020478	abnormal circadian sleep/wake cycle	Tfap2b<em1Sleep>/Tfap2b<+>	C57BL/6J-Tfap2b<em1Sleep>	N	32878901
MGI:7627368	F	MP:0012289	abnormal non-rapid eye movement sleep pattern	Tfap2b<em2Sleep>/Tfap2b<+>	C57BL/6J-Tfap2b<em2Sleep>	N	32878901
MGI:7627368	F	MP:0012287	increased frequency of paradoxical sleep	Tfap2b<em2Sleep>/Tfap2b<+>	C57BL/6J-Tfap2b<em2Sleep>	N	32878901
MGI:7627368	M	MP:0005386	behavior/neurological phenotype	Tfap2b<em2Sleep>/Tfap2b<+>	C57BL/6J-Tfap2b<em2Sleep>	Y	32878901
MGI:7627368	F	MP:0020478	abnormal circadian sleep/wake cycle	Tfap2b<em2Sleep>/Tfap2b<+>	C57BL/6J-Tfap2b<em2Sleep>	N	32878901
MGI:7627369	M	MP:0005386	behavior/neurological phenotype	Tfap2b<tm1b(EUCOMM)Wtsi>/Tfap2b<+>	involves: C57BL/6N * DBA/2	Y	32878901
MGI:7627369	F	MP:0020478	abnormal circadian sleep/wake cycle	Tfap2b<tm1b(EUCOMM)Wtsi>/Tfap2b<+>	involves: C57BL/6N * DBA/2	N	32878901
MGI:7627369	F	MP:0012289	abnormal non-rapid eye movement sleep pattern	Tfap2b<tm1b(EUCOMM)Wtsi>/Tfap2b<+>	involves: C57BL/6N * DBA/2	N	32878901
MGI:7628211	M	MP:0004182	abnormal spermiation	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0020869	immotile sperm	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0009230	abnormal sperm head morphology	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0031356	abnormal outer dense fiber morphology	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0005578	teratozoospermia	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0009376	abnormal manchette morphology	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0002216	abnormal seminiferous tubule morphology	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0009836	abnormal sperm principal piece morphology	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0030590	abnormal sperm fibrous sheath morphology	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0004852	decreased testis weight	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0002687	oligozoospermia	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0001932	abnormal spermiogenesis	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0008892	abnormal sperm flagellum morphology	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0001147	small testis	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0030591	absent sperm fibrous sheath	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0001925	male infertility	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0020451	decreased sperm progressive motility	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0002662	abnormal cauda epididymis morphology	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0009241	thick sperm flagellum	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628211	M	MP:0009838	abnormal sperm axoneme morphology	Ccdc183<em1Osb>/Ccdc183<em1Osb>	involves: C57BL/6 * DBA	N	37882665
MGI:7628342	M	MP:0009435	abnormal miniature inhibitory postsynaptic currents	Gm41261<em1Geh>/Gm41261<em1Geh>	C57BL/6J-Gm41261<em1Geh>	N	38373108
MGI:7628342	M	MP:0003546	decreased alcohol consumption	Gm41261<em1Geh>/Gm41261<em1Geh>	C57BL/6J-Gm41261<em1Geh>	N	38373108
MGI:7628342	M	MP:0014382	increased miniature inhibitory postsynaptic current frequency	Gm41261<em1Geh>/Gm41261<em1Geh>	C57BL/6J-Gm41261<em1Geh>	N	38373108
MGI:7628683	M	MP:0006035	abnormal mitochondrial morphology	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0009838	abnormal sperm axoneme morphology	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0001925	male infertility	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0005389	reproductive system phenotype	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	Y	38470475
MGI:7628683	M	MP:0009232	abnormal sperm nucleus morphology	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0008892	abnormal sperm flagellum morphology	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0009832	abnormal sperm mitochondrial sheath morphology	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0030590	abnormal sperm fibrous sheath morphology	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0009831	abnormal sperm midpiece morphology	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0004901	decreased male germ cell number	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0002687	oligozoospermia	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0002675	asthenozoospermia	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0020362	abnormal male germ cell physiology	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0009230	abnormal sperm head morphology	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0014052	increased male germ cell apoptosis	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0006380	abnormal spermatid morphology	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0014468	disorganized sperm mitochondrial sheath	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0008898	abnormal acrosome morphology	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628683	M	MP:0011635	abnormal mitochondrial crista morphology	Fbxo24<em1Syu>/Fbxo24<em1Syu>	involves: C57BL/6J	N	38470475
MGI:7628726	M	MP:0014431	increased chemokine level	Apoe<tm1Unc>/Apoe<tm1Unc>,Thbs4<tm1Olsa>/Thbs4<tm1Olsa>	involves: 129P2/OlaHsd * C57BL/6J	N	32686880
MGI:7628726	F	MP:0008593	increased circulating interleukin-10 level	Apoe<tm1Unc>/Apoe<tm1Unc>,Thbs4<tm1Olsa>/Thbs4<tm1Olsa>	involves: 129P2/OlaHsd * C57BL/6J	N	32686880
MGI:7628726	M	MP:0003982	increased cholesterol level	Apoe<tm1Unc>/Apoe<tm1Unc>,Thbs4<tm1Olsa>/Thbs4<tm1Olsa>	involves: 129P2/OlaHsd * C57BL/6J	N	32686880
MGI:7628726	M	MP:0005376	homeostasis/metabolism phenotype	Apoe<tm1Unc>/Apoe<tm1Unc>,Thbs4<tm1Olsa>/Thbs4<tm1Olsa>	involves: 129P2/OlaHsd * C57BL/6J	Y	32686880
MGI:7628726	F	MP:0008553	increased circulating tumor necrosis factor level	Apoe<tm1Unc>/Apoe<tm1Unc>,Thbs4<tm1Olsa>/Thbs4<tm1Olsa>	involves: 129P2/OlaHsd * C57BL/6J	N	32686880
MGI:7628890	F	MP:0001529	abnormal vocalization	1600014C10Rik<em1(IMPC)J>/1600014C10Rik<em1(IMPC)J>	C57BL/6NJ-1600014C10Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628890	F	MP:0002075	abnormal coat/hair pigmentation	1600014C10Rik<em1(IMPC)J>/1600014C10Rik<em1(IMPC)J>	C57BL/6NJ-1600014C10Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628891	F	MP:0000367	abnormal coat/ hair morphology	1700020A23Rik<em1(IMPC)Mbp>/1700020A23Rik<em1(IMPC)Mbp>	C57BL/6NCrl-1700020A23Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628892	F	MP:0000367	abnormal coat/ hair morphology	2310011J03Rik<em1(IMPC)Mbp>/2310011J03Rik<+>	C57BL/6NCrl-2310011J03Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628896	M	MP:0000367	abnormal coat/ hair morphology	4930558K02Rik<em1(IMPC)J>/4930558K02Rik<em1(IMPC)J>	C57BL/6NJ-4930558K02Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628897	F	MP:0005632	decreased circulating aspartate transaminase level	4933411K16Rik<em1(IMPC)J>/4933411K16Rik<em1(IMPC)J>	C57BL/6NJ-4933411K16Rik<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628898	M	MP:0009141	increased prepulse inhibition	5031439G07Rik<em1(IMPC)Mbp>/5031439G07Rik<em1(IMPC)Mbp>	C57BL/6NCrl-5031439G07Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628899	M	MP:0009476	enlarged cecum	6820408C15Rik<em1(IMPC)Mbp>/6820408C15Rik<em1(IMPC)Mbp>	C57BL/6NCrl-6820408C15Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628899	M	MP:0000494	abnormal cecum morphology	6820408C15Rik<em1(IMPC)Mbp>/6820408C15Rik<em1(IMPC)Mbp>	C57BL/6NCrl-6820408C15Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628900	M	MP:0013279	increased fasting circulating glucose level	A830018L16Rik<em1(IMPC)Mbp>/A830018L16Rik<em1(IMPC)Mbp>	C57BL/6NCrl-A830018L16Rik<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628901	F	MP:0001293	anophthalmia	Adam7<em1(IMPC)Ccpcz>/Adam7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Adam7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628901	F	MP:0002092	abnormal eye morphology	Adam7<em1(IMPC)Ccpcz>/Adam7<em1(IMPC)Ccpcz>	C57BL/6NCrl-Adam7<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628903	F	MP:0001325	abnormal retina morphology	Adgrf1<em1(IMPC)Ccpcz>/Adgrf1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Adgrf1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628903	M	MP:0000691	enlarged spleen	Adgrf1<em1(IMPC)Ccpcz>/Adgrf1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Adgrf1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628903	M	MP:0000266	abnormal heart morphology	Adgrf1<em1(IMPC)Ccpcz>/Adgrf1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Adgrf1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628903	M	MP:0000274	enlarged heart	Adgrf1<em1(IMPC)Ccpcz>/Adgrf1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Adgrf1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628903	M	MP:0000689	abnormal spleen morphology	Adgrf1<em1(IMPC)Ccpcz>/Adgrf1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Adgrf1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628904	F	MP:0010097	abnormal retina blood vessel morphology	Aff2<em1(IMPC)Hmgu>/Aff2<em1(IMPC)Hmgu>	C57BL/6NCrl-Aff2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628906	F	MP:0010053	decreased grip strength	Afmid<em1Llp>/Afmid<em1Llp>	C57BL/6NJ-Afmid<em1Llp>/J	N	MGI:5576271
MGI:7628907	M	MP:0000599	enlarged liver	Agpat2<em1(IMPC)Ccpcz>/Agpat2<+>	C57BL/6NCrl-Agpat2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628907	M	MP:0002135	abnormal kidney morphology	Agpat2<em1(IMPC)Ccpcz>/Agpat2<+>	C57BL/6NCrl-Agpat2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628907	M	MP:0000470	abnormal stomach morphology	Agpat2<em1(IMPC)Ccpcz>/Agpat2<+>	C57BL/6NCrl-Agpat2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628907	M	MP:0000689	abnormal spleen morphology	Agpat2<em1(IMPC)Ccpcz>/Agpat2<+>	C57BL/6NCrl-Agpat2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628907	F	MP:0001120	abnormal uterus morphology	Agpat2<em1(IMPC)Ccpcz>/Agpat2<+>	C57BL/6NCrl-Agpat2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628907	M	MP:0000598	abnormal liver morphology	Agpat2<em1(IMPC)Ccpcz>/Agpat2<+>	C57BL/6NCrl-Agpat2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628907	M	MP:0003068	enlarged kidney	Agpat2<em1(IMPC)Ccpcz>/Agpat2<+>	C57BL/6NCrl-Agpat2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628907	M	MP:0003883	enlarged stomach	Agpat2<em1(IMPC)Ccpcz>/Agpat2<+>	C57BL/6NCrl-Agpat2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628907	M	MP:0001147	small testis	Agpat2<em1(IMPC)Ccpcz>/Agpat2<+>	C57BL/6NCrl-Agpat2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628907	M	MP:0001146	abnormal testis morphology	Agpat2<em1(IMPC)Ccpcz>/Agpat2<+>	C57BL/6NCrl-Agpat2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628907	M	MP:0000691	enlarged spleen	Agpat2<em1(IMPC)Ccpcz>/Agpat2<+>	C57BL/6NCrl-Agpat2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628907	F	MP:0004906	enlarged uterus	Agpat2<em1(IMPC)Ccpcz>/Agpat2<+>	C57BL/6NCrl-Agpat2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628908	F	MP:0002590	increased mean corpuscular volume	Agtrap<em1(IMPC)Mbp>/Agtrap<em1(IMPC)Mbp>	C57BL/6NCrl-Agtrap<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628908	F	MP:0002606	increased basophil cell number	Agtrap<em1(IMPC)Mbp>/Agtrap<em1(IMPC)Mbp>	C57BL/6NCrl-Agtrap<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628908	M	MP:0020421	increased freezing behavior	Agtrap<em1(IMPC)Mbp>/Agtrap<em1(IMPC)Mbp>	C57BL/6NCrl-Agtrap<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628908	F	MP:0000219	increased neutrophil cell number	Agtrap<em1(IMPC)Mbp>/Agtrap<em1(IMPC)Mbp>	C57BL/6NCrl-Agtrap<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628909	F	MP:0000745	tremors	Alg12<em1(IMPC)J>/Alg12<+>	C57BL/6NJ-Alg12<em1(IMPC)J>/J	N	MGI:5576271
MGI:7628910	M	MP:0010053	decreased grip strength	Alkal2<em1(IMPC)J>/Alkal2<+>	C57BL/6NJ-Alkal2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628911	F	MP:0005287	narrow eye opening	Alkal2<em1(IMPC)J>/Alkal2<em1(IMPC)J>	C57BL/6NJ-Alkal2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628911	F	MP:0001314	cornea opacity	Alkal2<em1(IMPC)J>/Alkal2<em1(IMPC)J>	C57BL/6NJ-Alkal2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628913	M	MP:0012000	abnormal limb position	Anapc10<em1(IMPC)J>/Anapc10<+>	C57BL/6NJ-Anapc10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628914	M	MP:0010052	increased grip strength	Ankrd60<em1(IMPC)J>/Ankrd60<em1(IMPC)J>	C57BL/6NJ-Ankrd60<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628914	F	MP:0000194	increased circulating calcium level	Ankrd60<em1(IMPC)J>/Ankrd60<em1(IMPC)J>	C57BL/6NJ-Ankrd60<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628916	M	MP:0006243	impaired pupillary reflex	Arr3<em1(IMPC)J>/Y	C57BL/6NJ-Arr3<em1(IMPC)J>/J	N	MGI:5576271
MGI:7628917	M	MP:0009142	decreased prepulse inhibition	Asap2<em1(IMPC)Wtsi>/Asap2<em1(IMPC)Wtsi>	C57BL/6NCrl-Asap2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:7628919	F	MP:0001488	increased startle reflex	Atxn7l1<em1(IMPC)J>/Atxn7l1<em1(IMPC)J>	C57BL/6NJ-Atxn7l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628919	F	MP:0000745	tremors	Atxn7l1<em1(IMPC)J>/Atxn7l1<em1(IMPC)J>	C57BL/6NJ-Atxn7l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628921	F	MP:0001402	decreased locomotor activity	B4galnt4<em1(IMPC)J>/B4galnt4<em1(IMPC)J>	C57BL/6NJ-B4galnt4<em1(IMPC)J>/J	N	MGI:5576271
MGI:7628922	M	MP:0001406	abnormal gait	Brinp2<em1(IMPC)Wtsi>/Brinp2<em1(IMPC)Wtsi>	C57BL/6NCrl-Brinp2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:7628923	F	MP:0010024	increased total body fat amount	Brms1l<em1(IMPC)J>/Brms1l<em1(IMPC)J>	C57BL/6NJ-Brms1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628923	F	MP:0000063	decreased bone mineral density	Brms1l<em1(IMPC)J>/Brms1l<em1(IMPC)J>	C57BL/6NJ-Brms1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628923	F	MP:0003795	abnormal bone structure	Brms1l<em1(IMPC)J>/Brms1l<em1(IMPC)J>	C57BL/6NJ-Brms1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628923	F	MP:0010124	decreased bone mineral content	Brms1l<em1(IMPC)J>/Brms1l<em1(IMPC)J>	C57BL/6NJ-Brms1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628924	M	MP:0002135	abnormal kidney morphology	C2cd4c<em1(IMPC)Hmgu>/C2cd4c<em1(IMPC)Hmgu>	C57BL/6NCrl-C2cd4c<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628925	F	MP:0011110	preweaning lethality, incomplete penetrance	C2cd5<em1(IMPC)Tcp>/C2cd5<em1(IMPC)Tcp>	C57BL/6NCrl-C2cd5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628926	F	MP:0002989	small kidney	Casp8<em1(IMPC)Ccpcz>/Casp8<+>	C57BL/6NCrl-Casp8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628926	M	MP:0000266	abnormal heart morphology	Casp8<em1(IMPC)Ccpcz>/Casp8<+>	C57BL/6NCrl-Casp8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628926	F	MP:0002135	abnormal kidney morphology	Casp8<em1(IMPC)Ccpcz>/Casp8<+>	C57BL/6NCrl-Casp8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628926	F	MP:0000601	small liver	Casp8<em1(IMPC)Ccpcz>/Casp8<+>	C57BL/6NCrl-Casp8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628926	F	MP:0000598	abnormal liver morphology	Casp8<em1(IMPC)Ccpcz>/Casp8<+>	C57BL/6NCrl-Casp8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628926	M	MP:0000274	enlarged heart	Casp8<em1(IMPC)Ccpcz>/Casp8<+>	C57BL/6NCrl-Casp8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628928	M	MP:0002574	increased vertical activity	Ccdc148<em1(IMPC)Bay>/Ccdc148<em1(IMPC)Bay>	C57BL/6N-Ccdc148<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628929	F	MP:0001284	absent vibrissae	Ccdc184<em1(IMPC)J>/Ccdc184<em1(IMPC)J>	C57BL/6NJ-Ccdc184<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628930	M	MP:0000221	decreased leukocyte cell number	Ccdc32<em1(IMPC)J>/Ccdc32<+>	C57BL/6NJ-Ccdc32<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628932	F	MP:0005642	decreased mean corpuscular hemoglobin concentration	Ccdc66<em1(IMPC)Mbp>/Ccdc66<em1(IMPC)Mbp>	C57BL/6NCrl-Ccdc66<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628932	F	MP:0002608	increased hematocrit	Ccdc66<em1(IMPC)Mbp>/Ccdc66<em1(IMPC)Mbp>	C57BL/6NCrl-Ccdc66<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628932	F	MP:0005562	decreased mean corpuscular hemoglobin	Ccdc66<em1(IMPC)Mbp>/Ccdc66<em1(IMPC)Mbp>	C57BL/6NCrl-Ccdc66<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628933	M	MP:0010052	increased grip strength	Ccdc90b<em1(IMPC)J>/Ccdc90b<em1(IMPC)J>	C57BL/6NJ-Ccdc90b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628933	M	MP:0005635	decreased circulating bilirubin level	Ccdc90b<em1(IMPC)J>/Ccdc90b<em1(IMPC)J>	C57BL/6NJ-Ccdc90b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628934	M	MP:0010024	increased total body fat amount	Ccdc93<em1(IMPC)J>/Ccdc93<+>	C57BL/6NJ-Ccdc93<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628934	M	MP:0002834	decreased heart weight	Ccdc93<em1(IMPC)J>/Ccdc93<+>	C57BL/6NJ-Ccdc93<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628934	M	MP:0003961	decreased lean body mass	Ccdc93<em1(IMPC)J>/Ccdc93<+>	C57BL/6NJ-Ccdc93<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628935	M	MP:0012000	abnormal limb position	Ccl4<em1(IMPC)Bay>/Ccl4<em1(IMPC)Bay>	C57BL/6N-Ccl4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628935	M	MP:0000550	abnormal forelimb morphology	Ccl4<em1(IMPC)Bay>/Ccl4<em1(IMPC)Bay>	C57BL/6N-Ccl4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628936	M	MP:0000689	abnormal spleen morphology	Cd209c<em1(IMPC)Ccpcz>/Cd209c<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd209c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628936	M	MP:0002059	abnormal seminal vesicle morphology	Cd209c<em1(IMPC)Ccpcz>/Cd209c<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd209c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628936	M	MP:0000691	enlarged spleen	Cd209c<em1(IMPC)Ccpcz>/Cd209c<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cd209c<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628937	F	MP:0000745	tremors	Cdhr3<em1(IMPC)Wtsi>/Cdhr3<em1(IMPC)Wtsi>	C57BL/6NCrl-Cdhr3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:7628937	M	MP:0001510	abnormal coat appearance	Cdhr3<em1(IMPC)Wtsi>/Cdhr3<em1(IMPC)Wtsi>	C57BL/6NCrl-Cdhr3<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:7628938	M	MP:0002699	abnormal vitreous body morphology	Cdnf<em1(IMPC)Hmgu>/Cdnf<em1(IMPC)Hmgu>	C57BL/6NCrl-Cdnf<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628938	M	MP:0001325	abnormal retina morphology	Cdnf<em1(IMPC)Hmgu>/Cdnf<em1(IMPC)Hmgu>	C57BL/6NCrl-Cdnf<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628939	F	MP:0011100	preweaning lethality, complete penetrance	Cep104<em1(IMPC)Bay>/Cep104<em1(IMPC)Bay>	C57BL/6N-Cep104<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628940	F	MP:0001926	female infertility	Cep70<em1(IMPC)Bay>/Cep70<em1(IMPC)Bay>	C57BL/6N-Cep70<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628941	M	MP:0005635	decreased circulating bilirubin level	Cfap107<em1(IMPC)J>/Cfap107<em1(IMPC)J>	C57BL/6NJ-Cfap107<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628942	M	MP:0000218	increased leukocyte cell number	Cfap20dc<em1(IMPC)J>/Cfap20dc<em1(IMPC)J>	C57BL/6NJ-Cfap20dc<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628942	M	MP:0002834	decreased heart weight	Cfap20dc<em1(IMPC)J>/Cfap20dc<em1(IMPC)J>	C57BL/6NJ-Cfap20dc<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628943	M	MP:0001340	abnormal eyelid morphology	Cfap47<em1(IMPC)Hmgu>/Y	C57BL/6NCrl-Cfap47<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628944	F	MP:0001340	abnormal eyelid morphology	Cfap47<em1(IMPC)Hmgu>/Cfap47<em1(IMPC)Hmgu>	C57BL/6NCrl-Cfap47<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628944	F	MP:0003961	decreased lean body mass	Cfap47<em1(IMPC)Hmgu>/Cfap47<em1(IMPC)Hmgu>	C57BL/6NCrl-Cfap47<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628944	F	MP:0004953	decreased spleen weight	Cfap47<em1(IMPC)Hmgu>/Cfap47<em1(IMPC)Hmgu>	C57BL/6NCrl-Cfap47<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628944	F	MP:0010024	increased total body fat amount	Cfap47<em1(IMPC)Hmgu>/Cfap47<em1(IMPC)Hmgu>	C57BL/6NCrl-Cfap47<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628945	F	MP:0010053	decreased grip strength	Chic1<em1(IMPC)Tcp>/Chic1<em1(IMPC)Tcp>	C57BL/6NCrl-Chic1<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628946	M	MP:0001406	abnormal gait	Chrnb1<em1(IMPC)Bay>/Chrnb1<+>	C57BL/6N-Chrnb1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628946	M	MP:0001392	abnormal locomotor behavior	Chrnb1<em1(IMPC)Bay>/Chrnb1<+>	C57BL/6N-Chrnb1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628947	F	MP:0011100	preweaning lethality, complete penetrance	Chrnb1<em1(IMPC)Bay>/Chrnb1<em1(IMPC)Bay>	C57BL/6N-Chrnb1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628948	F	MP:0003731	abnormal retina outer nuclear layer morphology	Clpsl2<em1(IMPC)Bay>/Clpsl2<em1(IMPC)Bay>	C57BL/6N-Clpsl2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628948	F	MP:0011964	increased total retina thickness	Clpsl2<em1(IMPC)Bay>/Clpsl2<em1(IMPC)Bay>	C57BL/6N-Clpsl2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628949	M	MP:0000274	enlarged heart	Cobl<em1(IMPC)Ccpcz>/Cobl<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cobl<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628949	M	MP:0000266	abnormal heart morphology	Cobl<em1(IMPC)Ccpcz>/Cobl<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cobl<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628949	F	MP:0000703	abnormal thymus morphology	Cobl<em1(IMPC)Ccpcz>/Cobl<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cobl<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628949	M	MP:0013772	increased effector memory T-helper cell number	Cobl<em1(IMPC)Ccpcz>/Cobl<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cobl<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628949	F	MP:0000709	enlarged thymus	Cobl<em1(IMPC)Ccpcz>/Cobl<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cobl<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628950	F	MP:0000703	abnormal thymus morphology	Cops8<em1(IMPC)Ccpcz>/Cops8<+>	C57BL/6NCrl-Cops8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628950	M	MP:0000274	enlarged heart	Cops8<em1(IMPC)Ccpcz>/Cops8<+>	C57BL/6NCrl-Cops8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628950	M	MP:0000689	abnormal spleen morphology	Cops8<em1(IMPC)Ccpcz>/Cops8<+>	C57BL/6NCrl-Cops8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628950	M	MP:0000266	abnormal heart morphology	Cops8<em1(IMPC)Ccpcz>/Cops8<+>	C57BL/6NCrl-Cops8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628950	F	MP:0000709	enlarged thymus	Cops8<em1(IMPC)Ccpcz>/Cops8<+>	C57BL/6NCrl-Cops8<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628953	F	MP:0020420	abnormal freezing behavior	Crocc2<em1(IMPC)Ccpcz>/Crocc2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Crocc2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628953	M	MP:0000691	enlarged spleen	Crocc2<em1(IMPC)Ccpcz>/Crocc2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Crocc2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628953	M	MP:0000266	abnormal heart morphology	Crocc2<em1(IMPC)Ccpcz>/Crocc2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Crocc2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628953	F	MP:0002135	abnormal kidney morphology	Crocc2<em1(IMPC)Ccpcz>/Crocc2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Crocc2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628953	M	MP:0000274	enlarged heart	Crocc2<em1(IMPC)Ccpcz>/Crocc2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Crocc2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628953	M	MP:0000689	abnormal spleen morphology	Crocc2<em1(IMPC)Ccpcz>/Crocc2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Crocc2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628954	M	MP:0001392	abnormal locomotor behavior	Cryba4<em1(IMPC)Bay>/Cryba4<em1(IMPC)Bay>	C57BL/6N-Cryba4<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628957	F	MP:0005635	decreased circulating bilirubin level	Ctu1<em1(IMPC)J>/Ctu1<+>	C57BL/6NJ-Ctu1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628959	M	MP:0001146	abnormal testis morphology	Cyth4<em1(IMPC)Ccpcz>/Cyth4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cyth4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628959	M	MP:0006415	absent testes	Cyth4<em1(IMPC)Ccpcz>/Cyth4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cyth4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628959	F	MP:0008810	increased circulating iron level	Cyth4<em1(IMPC)Ccpcz>/Cyth4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Cyth4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628960	F	MP:0009142	decreased prepulse inhibition	Dctn6<em1(IMPC)J>/Dctn6<+>	C57BL/6NJ-Dctn6<em1(IMPC)J>/J	N	MGI:5576271
MGI:7628962	M	MP:0020870	decreased thigmotaxis	Defb34<em1(IMPC)Bay>/Defb34<em1(IMPC)Bay>	C57BL/6N-Defb34<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628962	M	MP:0001402	decreased locomotor activity	Defb34<em1(IMPC)Bay>/Defb34<em1(IMPC)Bay>	C57BL/6N-Defb34<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628963	M	MP:0000745	tremors	Dhrs1<em1(IMPC)J>/Dhrs1<em1(IMPC)J>	C57BL/6NJ-Dhrs1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628964	M	MP:0001556	increased circulating HDL cholesterol level	Dhrs7b<em1(IMPC)Mbp>/Dhrs7b<+>	C57BL/6NCrl-Dhrs7b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628964	M	MP:0002941	increased circulating alanine transaminase level	Dhrs7b<em1(IMPC)Mbp>/Dhrs7b<+>	C57BL/6NCrl-Dhrs7b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628966	F	MP:0010024	increased total body fat amount	Dnai2<em1(IMPC)Tcp>/Dnai2<+>	C57BL/6NCrl-Dnai2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628966	M	MP:0000702	enlarged lymph nodes	Dnai2<em1(IMPC)Tcp>/Dnai2<+>	C57BL/6NCrl-Dnai2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628966	F	MP:0003961	decreased lean body mass	Dnai2<em1(IMPC)Tcp>/Dnai2<+>	C57BL/6NCrl-Dnai2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628966	M	MP:0011874	enlarged urinary bladder	Dnai2<em1(IMPC)Tcp>/Dnai2<+>	C57BL/6NCrl-Dnai2<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628967	F	MP:0005343	increased circulating aspartate transaminase level	Dnajb14<em1(IMPC)Hmgu>/Dnajb14<+>	C57BL/6NCrl-Dnajb14<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628969	M	MP:0001486	abnormal startle reflex	Ear6<em1(IMPC)Bay>/Ear6<em1(IMPC)Bay>	C57BL/6N-Ear6<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628970	F	MP:0002764	short tibia	Echs1<em1(IMPC)Hmgu>/Echs1<+>	C57BL/6NCrl-Echs1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628971	F	MP:0001523	impaired righting response	Eefsec<em1(IMPC)Hmgu>/Eefsec<+>	C57BL/6NCrl-Eefsec<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628974	F	MP:0001399	hyperactivity	Eif4a2<em1(IMPC)J>/Eif4a2<em1(IMPC)J>	C57BL/6NJ-Eif4a2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628975	F	MP:0002834	decreased heart weight	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0010097	abnormal retina blood vessel morphology	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	M	MP:0002599	increased mean platelet volume	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0002764	short tibia	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0002757	decreased vertical activity	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0010024	increased total body fat amount	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0010393	shortened QRS complex duration	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0003795	abnormal bone structure	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0001322	abnormal iris morphology	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0006243	impaired pupillary reflex	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0005278	abnormal cholesterol homeostasis	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0005292	improved glucose tolerance	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0010068	decreased red blood cell distribution width	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0010511	shortened PR interval	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0003900	shortened QT interval	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0001402	decreased locomotor activity	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0010124	decreased bone mineral content	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0003961	decreased lean body mass	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	M	MP:0001556	increased circulating HDL cholesterol level	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0013279	increased fasting circulating glucose level	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	M	MP:0002968	increased circulating alkaline phosphatase level	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628975	F	MP:0002792	abnormal retina vasculature morphology	Elovl5<em1(IMPC)Tcp>/Elovl5<em1(IMPC)Tcp>	C57BL/6NCrl-Elovl5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628977	M	MP:0002574	increased vertical activity	Elp4<em1(IMPC)Tcp>/Elp4<+>	C57BL/6NCrl-Elp4<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7628980	M	MP:0003896	prolonged PR interval	Eml4<em1(IMPC)J>/Eml4<+>	C57BL/6NJ-Eml4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628980	M	MP:0002075	abnormal coat/hair pigmentation	Eml4<em1(IMPC)J>/Eml4<+>	C57BL/6NJ-Eml4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628980	M	MP:0001529	abnormal vocalization	Eml4<em1(IMPC)J>/Eml4<+>	C57BL/6NJ-Eml4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628981	F	MP:0002060	abnormal skin morphology	Endov<em1(IMPC)Mbp>/Endov<em1(IMPC)Mbp>	C57BL/6NCrl-Endov<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628981	F	MP:0002968	increased circulating alkaline phosphatase level	Endov<em1(IMPC)Mbp>/Endov<em1(IMPC)Mbp>	C57BL/6NCrl-Endov<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628981	M	MP:0005419	decreased circulating serum albumin level	Endov<em1(IMPC)Mbp>/Endov<em1(IMPC)Mbp>	C57BL/6NCrl-Endov<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628982	F	MP:0000691	enlarged spleen	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628982	M	MP:0000703	abnormal thymus morphology	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628982	M	MP:0000274	enlarged heart	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628982	F	MP:0004122	abnormal sinus arrhythmia	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628982	F	MP:0001926	female infertility	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628982	F	MP:0001417	decreased exploration in new environment	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628982	F	MP:0010935	increased airway resistance	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628982	M	MP:0000266	abnormal heart morphology	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628982	F	MP:0001262	decreased body weight	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628982	M	MP:0000706	small thymus	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628982	M	MP:0000627	abnormal mammary gland morphology	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628982	F	MP:0000689	abnormal spleen morphology	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628982	M	MP:0001925	male infertility	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628982	F	MP:0005385	cardiovascular system phenotype	Enpp1<em1(IMPC)Ccpcz>/Enpp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Enpp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628983	F	MP:0010052	increased grip strength	Etfa<em1(IMPC)J>/Etfa<+>	C57BL/6NJ-Etfa<em1(IMPC)J>/J	N	MGI:5576271
MGI:7628985	M	MP:0002100	abnormal tooth morphology	Etnppl<em1(IMPC)Hmgu>/Etnppl<em1(IMPC)Hmgu>	C57BL/6NCrl-Etnppl<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628985	F	MP:0000745	tremors	Etnppl<em1(IMPC)Hmgu>/Etnppl<em1(IMPC)Hmgu>	C57BL/6NCrl-Etnppl<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628986	F	MP:0003068	enlarged kidney	Faim2<em1(IMPC)Ccpcz>/Faim2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Faim2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628986	F	MP:0002135	abnormal kidney morphology	Faim2<em1(IMPC)Ccpcz>/Faim2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Faim2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628986	F	MP:0003917	increased kidney weight	Faim2<em1(IMPC)Ccpcz>/Faim2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Faim2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628986	M	MP:0000692	small spleen	Faim2<em1(IMPC)Ccpcz>/Faim2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Faim2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628986	M	MP:0000689	abnormal spleen morphology	Faim2<em1(IMPC)Ccpcz>/Faim2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Faim2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628988	F	MP:0002092	abnormal eye morphology	Fam229b<em1(IMPC)Mbp>/Fam229b<em1(IMPC)Mbp>	C57BL/6NCrl-Fam229b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628988	F	MP:0002606	increased basophil cell number	Fam229b<em1(IMPC)Mbp>/Fam229b<em1(IMPC)Mbp>	C57BL/6NCrl-Fam229b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628990	M	MP:0000572	abnormal autopod morphology	Fam91a1<em1(IMPC)Bay>/Fam91a1<+>	C57BL/6N-Fam91a1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628990	M	MP:0000443	abnormal snout morphology	Fam91a1<em1(IMPC)Bay>/Fam91a1<+>	C57BL/6N-Fam91a1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628991	F	MP:0001392	abnormal locomotor behavior	Fam91a1<em1(IMPC)Bay>/Fam91a1<em1(IMPC)Bay>	C57BL/6N-Fam91a1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7628992	F	MP:0005632	decreased circulating aspartate transaminase level	Fbxo48<em1(IMPC)J>/Fbxo48<em1(IMPC)J>	C57BL/6NJ-Fbxo48<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628993	F	MP:0000703	abnormal thymus morphology	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	M	MP:0002059	abnormal seminal vesicle morphology	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0009142	decreased prepulse inhibition	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0000709	enlarged thymus	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0000689	abnormal spleen morphology	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0001489	decreased startle reflex	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0002989	small kidney	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0000598	abnormal liver morphology	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0002339	abnormal lymph node morphology	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	M	MP:0000274	enlarged heart	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0000702	enlarged lymph nodes	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0001120	abnormal uterus morphology	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	M	MP:0002060	abnormal skin morphology	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0000691	enlarged spleen	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0003918	decreased kidney weight	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	M	MP:0000470	abnormal stomach morphology	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0002135	abnormal kidney morphology	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0002100	abnormal tooth morphology	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	F	MP:0005568	increased circulating total protein level	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	M	MP:0000266	abnormal heart morphology	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628993	M	MP:0003883	enlarged stomach	Fgf20<em1(IMPC)Ccpcz>/Fgf20<em1(IMPC)Ccpcz>	C57BL/6NCrl-Fgf20<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628994	F	MP:0013279	increased fasting circulating glucose level	Fibin<em1(IMPC)J>/Fibin<em1(IMPC)J>	C57BL/6NJ-Fibin<em1(IMPC)J>/J	N	MGI:5576271
MGI:7628995	M	MP:0003961	decreased lean body mass	Fitm1<em1(IMPC)J>/Fitm1<em1(IMPC)J>	C57BL/6NJ-Fitm1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628995	M	MP:0010024	increased total body fat amount	Fitm1<em1(IMPC)J>/Fitm1<em1(IMPC)J>	C57BL/6NJ-Fitm1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7628996	F	MP:0002135	abnormal kidney morphology	Flacc1<em1(IMPC)Mbp>/Flacc1<em1(IMPC)Mbp>	C57BL/6NCrl-Flacc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628996	F	MP:0002060	abnormal skin morphology	Flacc1<em1(IMPC)Mbp>/Flacc1<em1(IMPC)Mbp>	C57BL/6NCrl-Flacc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628996	F	MP:0002989	small kidney	Flacc1<em1(IMPC)Mbp>/Flacc1<em1(IMPC)Mbp>	C57BL/6NCrl-Flacc1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7628997	M	MP:0000706	small thymus	Fnip1<em1(IMPC)Ccpcz>/Fnip1<+>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628997	M	MP:0010895	increased lung compliance	Fnip1<em1(IMPC)Ccpcz>/Fnip1<+>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628997	M	MP:0000627	abnormal mammary gland morphology	Fnip1<em1(IMPC)Ccpcz>/Fnip1<+>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628997	F	MP:0020421	increased freezing behavior	Fnip1<em1(IMPC)Ccpcz>/Fnip1<+>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628997	M	MP:0000703	abnormal thymus morphology	Fnip1<em1(IMPC)Ccpcz>/Fnip1<+>	C57BL/6NCrl-Fnip1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7628998	M	MP:0001325	abnormal retina morphology	Foxd2<em1(IMPC)Hmgu>/Foxd2<+>	C57BL/6NCrl-Foxd2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628999	F	MP:0002757	decreased vertical activity	Foxd2<em1(IMPC)Hmgu>/Foxd2<em1(IMPC)Hmgu>	C57BL/6NCrl-Foxd2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628999	M	MP:0002764	short tibia	Foxd2<em1(IMPC)Hmgu>/Foxd2<em1(IMPC)Hmgu>	C57BL/6NCrl-Foxd2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7628999	F	MP:0001402	decreased locomotor activity	Foxd2<em1(IMPC)Hmgu>/Foxd2<em1(IMPC)Hmgu>	C57BL/6NCrl-Foxd2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629000	M	MP:0010052	increased grip strength	Fscn3<em1(IMPC)J>/Fscn3<em1(IMPC)J>	C57BL/6NJ-Fscn3<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629001	M	MP:0000063	decreased bone mineral density	Fst<em1(IMPC)Wtsi>/Fst<+>	C57BL/6NCrl-Fst<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:7629003	F	MP:0002591	decreased mean corpuscular volume	Gak<em1(IMPC)Ccpcz>/Gak<+>	C57BL/6NCrl-Gak<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629003	M	MP:0000266	abnormal heart morphology	Gak<em1(IMPC)Ccpcz>/Gak<+>	C57BL/6NCrl-Gak<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629003	M	MP:0010067	increased red blood cell distribution width	Gak<em1(IMPC)Ccpcz>/Gak<+>	C57BL/6NCrl-Gak<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629003	M	MP:0000274	enlarged heart	Gak<em1(IMPC)Ccpcz>/Gak<+>	C57BL/6NCrl-Gak<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629003	F	MP:0000709	enlarged thymus	Gak<em1(IMPC)Ccpcz>/Gak<+>	C57BL/6NCrl-Gak<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629003	M	MP:0002135	abnormal kidney morphology	Gak<em1(IMPC)Ccpcz>/Gak<+>	C57BL/6NCrl-Gak<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629003	M	MP:0003917	increased kidney weight	Gak<em1(IMPC)Ccpcz>/Gak<+>	C57BL/6NCrl-Gak<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629003	M	MP:0003068	enlarged kidney	Gak<em1(IMPC)Ccpcz>/Gak<+>	C57BL/6NCrl-Gak<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629003	F	MP:0000627	abnormal mammary gland morphology	Gak<em1(IMPC)Ccpcz>/Gak<+>	C57BL/6NCrl-Gak<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629003	F	MP:0000703	abnormal thymus morphology	Gak<em1(IMPC)Ccpcz>/Gak<+>	C57BL/6NCrl-Gak<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629005	M	MP:0003131	increased erythrocyte cell number	Gimap7<em1(IMPC)Tcp>/Gimap7<+>	C57BL/6NCrl-Gimap7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629006	M	MP:0002092	abnormal eye morphology	Gimap7<em1(IMPC)Tcp>/Gimap7<em1(IMPC)Tcp>	C57BL/6NCrl-Gimap7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629006	M	MP:0011110	preweaning lethality, incomplete penetrance	Gimap7<em1(IMPC)Tcp>/Gimap7<em1(IMPC)Tcp>	C57BL/6NCrl-Gimap7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629008	F	MP:0000702	enlarged lymph nodes	Gnl2<em1(IMPC)Ccpcz>/Gnl2<+>	C57BL/6NCrl-Gnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629008	M	MP:0010895	increased lung compliance	Gnl2<em1(IMPC)Ccpcz>/Gnl2<+>	C57BL/6NCrl-Gnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629008	F	MP:0000691	enlarged spleen	Gnl2<em1(IMPC)Ccpcz>/Gnl2<+>	C57BL/6NCrl-Gnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629008	F	MP:0002339	abnormal lymph node morphology	Gnl2<em1(IMPC)Ccpcz>/Gnl2<+>	C57BL/6NCrl-Gnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629008	F	MP:0000689	abnormal spleen morphology	Gnl2<em1(IMPC)Ccpcz>/Gnl2<+>	C57BL/6NCrl-Gnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629008	M	MP:0011045	decreased lung elastance	Gnl2<em1(IMPC)Ccpcz>/Gnl2<+>	C57BL/6NCrl-Gnl2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629010	M	MP:0001157	small seminal vesicle	Gpatch4<em1(IMPC)Ccpcz>/Gpatch4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpatch4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629010	F	MP:0002591	decreased mean corpuscular volume	Gpatch4<em1(IMPC)Ccpcz>/Gpatch4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpatch4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629010	M	MP:0013279	increased fasting circulating glucose level	Gpatch4<em1(IMPC)Ccpcz>/Gpatch4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpatch4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629010	F	MP:0020421	increased freezing behavior	Gpatch4<em1(IMPC)Ccpcz>/Gpatch4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpatch4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629010	M	MP:0000689	abnormal spleen morphology	Gpatch4<em1(IMPC)Ccpcz>/Gpatch4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpatch4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629010	M	MP:0003961	decreased lean body mass	Gpatch4<em1(IMPC)Ccpcz>/Gpatch4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpatch4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629010	M	MP:0000692	small spleen	Gpatch4<em1(IMPC)Ccpcz>/Gpatch4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpatch4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629010	M	MP:0002059	abnormal seminal vesicle morphology	Gpatch4<em1(IMPC)Ccpcz>/Gpatch4<em1(IMPC)Ccpcz>	C57BL/6NCrl-Gpatch4<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629011	M	MP:0005635	decreased circulating bilirubin level	Gpn1<em1(IMPC)J>/Gpn1<+>	C57BL/6NJ-Gpn1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629011	M	MP:0005559	increased circulating glucose level	Gpn1<em1(IMPC)J>/Gpn1<+>	C57BL/6NJ-Gpn1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629012	M	MP:0002968	increased circulating alkaline phosphatase level	Gpr87<tm1.1(KOMP)Vlcg>/Gpr87<tm1.1(KOMP)Vlcg>	C57BL/6N-Gpr87<tm1.1(KOMP)Vlcg>/J	N	MGI:5576271
MGI:7629014	M	MP:0000221	decreased leukocyte cell number	Gtf2a1l<em1(IMPC)J>/Gtf2a1l<em1(IMPC)J>	C57BL/6NJ-Gtf2a1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629014	F	MP:0005568	increased circulating total protein level	Gtf2a1l<em1(IMPC)J>/Gtf2a1l<em1(IMPC)J>	C57BL/6NJ-Gtf2a1l<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629016	F	MP:0010123	increased bone mineral content	H2bc21<em1(IMPC)Bay>/H2bc21<+>	C57BL/6N-H2bc21<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629016	F	MP:0003795	abnormal bone structure	H2bc21<em1(IMPC)Bay>/H2bc21<+>	C57BL/6N-H2bc21<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629017	M	MP:0003917	increased kidney weight	Hcls1<em1(IMPC)Ccpcz>/Hcls1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hcls1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629017	M	MP:0001147	small testis	Hcls1<em1(IMPC)Ccpcz>/Hcls1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hcls1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629017	F	MP:0002092	abnormal eye morphology	Hcls1<em1(IMPC)Ccpcz>/Hcls1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hcls1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629017	F	MP:0000703	abnormal thymus morphology	Hcls1<em1(IMPC)Ccpcz>/Hcls1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hcls1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629017	F	MP:0001333	absent optic nerve	Hcls1<em1(IMPC)Ccpcz>/Hcls1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hcls1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629017	M	MP:0001146	abnormal testis morphology	Hcls1<em1(IMPC)Ccpcz>/Hcls1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hcls1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629017	F	MP:0000709	enlarged thymus	Hcls1<em1(IMPC)Ccpcz>/Hcls1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hcls1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629020	M	MP:0000691	enlarged spleen	Hormad2<em1(IMPC)Ccpcz>/Hormad2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hormad2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629020	M	MP:0001146	abnormal testis morphology	Hormad2<em1(IMPC)Ccpcz>/Hormad2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hormad2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629020	M	MP:0000627	abnormal mammary gland morphology	Hormad2<em1(IMPC)Ccpcz>/Hormad2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hormad2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629020	M	MP:0001147	small testis	Hormad2<em1(IMPC)Ccpcz>/Hormad2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hormad2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629020	M	MP:0000692	small spleen	Hormad2<em1(IMPC)Ccpcz>/Hormad2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hormad2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629020	M	MP:0002311	abnormal inspiratory capacity	Hormad2<em1(IMPC)Ccpcz>/Hormad2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hormad2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629020	M	MP:0000689	abnormal spleen morphology	Hormad2<em1(IMPC)Ccpcz>/Hormad2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hormad2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629020	M	MP:0011045	decreased lung elastance	Hormad2<em1(IMPC)Ccpcz>/Hormad2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hormad2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629020	M	MP:0001925	male infertility	Hormad2<em1(IMPC)Ccpcz>/Hormad2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hormad2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629020	M	MP:0001417	decreased exploration in new environment	Hormad2<em1(IMPC)Ccpcz>/Hormad2<em1(IMPC)Ccpcz>	C57BL/6NCrl-Hormad2<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629021	F	MP:0013279	increased fasting circulating glucose level	Hsd17b8<em1(IMPC)J>/Hsd17b8<em1(IMPC)J>	C57BL/6NJ-Hsd17b8<em1(IMPC)J>/J	N	MGI:5576271
MGI:7629022	M	MP:0010025	decreased total body fat amount	Idua<em1(IMPC)Hmgu>/Idua<em1(IMPC)Hmgu>	C57BL/6NCrl-Idua<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629022	M	MP:0001200	thick skin	Idua<em1(IMPC)Hmgu>/Idua<em1(IMPC)Hmgu>	C57BL/6NCrl-Idua<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629022	F	MP:0010053	decreased grip strength	Idua<em1(IMPC)Hmgu>/Idua<em1(IMPC)Hmgu>	C57BL/6NCrl-Idua<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629022	M	MP:0001303	abnormal lens morphology	Idua<em1(IMPC)Hmgu>/Idua<em1(IMPC)Hmgu>	C57BL/6NCrl-Idua<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629023	F	MP:0002792	abnormal retina vasculature morphology	Ifi205<em1(IMPC)Tcp>/Ifi205<em1(IMPC)Tcp>	C57BL/6NCrl-Ifi205<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629023	F	MP:0010097	abnormal retina blood vessel morphology	Ifi205<em1(IMPC)Tcp>/Ifi205<em1(IMPC)Tcp>	C57BL/6NCrl-Ifi205<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629023	F	MP:0002060	abnormal skin morphology	Ifi205<em1(IMPC)Tcp>/Ifi205<em1(IMPC)Tcp>	C57BL/6NCrl-Ifi205<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629023	M	MP:0003179	thrombocytopenia	Ifi205<em1(IMPC)Tcp>/Ifi205<em1(IMPC)Tcp>	C57BL/6NCrl-Ifi205<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629023	M	MP:0002608	increased hematocrit	Ifi205<em1(IMPC)Tcp>/Ifi205<em1(IMPC)Tcp>	C57BL/6NCrl-Ifi205<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629024	F	MP:0010506	prolonged RR interval	Impact<em1(IMPC)Ccpcz>/Impact<em1(IMPC)Ccpcz>	C57BL/6NCrl-Impact<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629024	M	MP:0000702	enlarged lymph nodes	Impact<em1(IMPC)Ccpcz>/Impact<em1(IMPC)Ccpcz>	C57BL/6NCrl-Impact<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629024	F	MP:0004122	abnormal sinus arrhythmia	Impact<em1(IMPC)Ccpcz>/Impact<em1(IMPC)Ccpcz>	C57BL/6NCrl-Impact<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629024	F	MP:0004156	abnormal QT variability	Impact<em1(IMPC)Ccpcz>/Impact<em1(IMPC)Ccpcz>	C57BL/6NCrl-Impact<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629024	M	MP:0013279	increased fasting circulating glucose level	Impact<em1(IMPC)Ccpcz>/Impact<em1(IMPC)Ccpcz>	C57BL/6NCrl-Impact<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629024	M	MP:0001175	abnormal lung morphology	Impact<em1(IMPC)Ccpcz>/Impact<em1(IMPC)Ccpcz>	C57BL/6NCrl-Impact<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629024	M	MP:0002339	abnormal lymph node morphology	Impact<em1(IMPC)Ccpcz>/Impact<em1(IMPC)Ccpcz>	C57BL/6NCrl-Impact<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629024	M	MP:0004882	enlarged lung	Impact<em1(IMPC)Ccpcz>/Impact<em1(IMPC)Ccpcz>	C57BL/6NCrl-Impact<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629024	F	MP:0005385	cardiovascular system phenotype	Impact<em1(IMPC)Ccpcz>/Impact<em1(IMPC)Ccpcz>	C57BL/6NCrl-Impact<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629025	M	MP:0005635	decreased circulating bilirubin level	Irgq<em1(IMPC)J>/Irgq<em1(IMPC)J>	C57BL/6NJ-Irgq<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629025	M	MP:0001556	increased circulating HDL cholesterol level	Irgq<em1(IMPC)J>/Irgq<em1(IMPC)J>	C57BL/6NJ-Irgq<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629026	M	MP:0001552	increased circulating triglyceride level	Itgbl1<em1(IMPC)Kmpc>/Itgbl1<em1(IMPC)Kmpc>	C57BL/6NTac-Itgbl1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7629026	M	MP:0002059	abnormal seminal vesicle morphology	Itgbl1<em1(IMPC)Kmpc>/Itgbl1<em1(IMPC)Kmpc>	C57BL/6NTac-Itgbl1<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7629028	M	MP:0000556	abnormal hindlimb morphology	Klhl17<em1(IMPC)Bay>/Klhl17<em1(IMPC)Bay>	C57BL/6N-Klhl17<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629028	M	MP:0001406	abnormal gait	Klhl17<em1(IMPC)Bay>/Klhl17<em1(IMPC)Bay>	C57BL/6N-Klhl17<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629028	M	MP:0000443	abnormal snout morphology	Klhl17<em1(IMPC)Bay>/Klhl17<em1(IMPC)Bay>	C57BL/6N-Klhl17<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629029	M	MP:0008078	increased CD8-positive, alpha-beta T cell number	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0001146	abnormal testis morphology	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0002059	abnormal seminal vesicle morphology	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0000266	abnormal heart morphology	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	F	MP:0000703	abnormal thymus morphology	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0003068	enlarged kidney	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0001175	abnormal lung morphology	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	F	MP:0003450	enlarged pancreas	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0002135	abnormal kidney morphology	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	F	MP:0002311	abnormal inspiratory capacity	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	F	MP:0005012	decreased eosinophil cell number	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0000274	enlarged heart	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	F	MP:0001944	abnormal pancreas morphology	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	F	MP:0000709	enlarged thymus	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	F	MP:0013436	increased CD8-positive, naive alpha-beta T cell number	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0005015	increased T cell number	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0000689	abnormal spleen morphology	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0001157	small seminal vesicle	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0013763	increased T-helper cell number	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0008074	increased CD4-positive, alpha-beta T cell number	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0000692	small spleen	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629029	M	MP:0001147	small testis	Klhl6<em1(IMPC)Ccpcz>/Klhl6<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klhl6<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629030	F	MP:0000703	abnormal thymus morphology	Klk10<em1(IMPC)Ccpcz>/Klk10<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klk10<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629030	F	MP:0005385	cardiovascular system phenotype	Klk10<em1(IMPC)Ccpcz>/Klk10<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klk10<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629030	F	MP:0000709	enlarged thymus	Klk10<em1(IMPC)Ccpcz>/Klk10<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klk10<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629030	M	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number	Klk10<em1(IMPC)Ccpcz>/Klk10<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klk10<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629030	M	MP:0010024	increased total body fat amount	Klk10<em1(IMPC)Ccpcz>/Klk10<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klk10<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629030	F	MP:0004122	abnormal sinus arrhythmia	Klk10<em1(IMPC)Ccpcz>/Klk10<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klk10<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629030	M	MP:0003019	increased circulating chloride level	Klk10<em1(IMPC)Ccpcz>/Klk10<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klk10<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629030	M	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number	Klk10<em1(IMPC)Ccpcz>/Klk10<em1(IMPC)Ccpcz>	C57BL/6NCrl-Klk10<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629031	M	MP:0005561	increased mean corpuscular hemoglobin	Kprp<em1(IMPC)Mbp>/Kprp<em1(IMPC)Mbp>	C57BL/6NCrl-Kprp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629031	M	MP:0005641	increased mean corpuscular hemoglobin concentration	Kprp<em1(IMPC)Mbp>/Kprp<em1(IMPC)Mbp>	C57BL/6NCrl-Kprp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629032	M	MP:0001175	abnormal lung morphology	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	M	MP:0013436	increased CD8-positive, naive alpha-beta T cell number	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	M	MP:0000691	enlarged spleen	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	M	MP:0002631	abnormal epididymis morphology	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	F	MP:0003020	decreased circulating chloride level	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	F	MP:0000709	enlarged thymus	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	M	MP:0002059	abnormal seminal vesicle morphology	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	M	MP:0013772	increased effector memory T-helper cell number	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	M	MP:0001146	abnormal testis morphology	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	F	MP:0000703	abnormal thymus morphology	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	M	MP:0000689	abnormal spleen morphology	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	M	MP:0001147	small testis	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	M	MP:0008045	decreased NK cell number	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	M	MP:0004930	small epididymis	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	M	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	M	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629032	M	MP:0004952	increased spleen weight	Krt1<em1(IMPC)Ccpcz>/Krt1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Krt1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629033	F	MP:0000367	abnormal coat/ hair morphology	Krt23<em1(IMPC)J>/Krt23<em1(IMPC)J>	C57BL/6NJ-Krt23<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629034	M	MP:0001392	abnormal locomotor behavior	Krt40<em1(IMPC)J>/Krt40<em1(IMPC)J>	C57BL/6NJ-Krt40<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629035	M	MP:0000367	abnormal coat/ hair morphology	Krt71<em1(IMPC)Bay>/Krt71<em1(IMPC)Bay>	C57BL/6N-Krt71<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629035	M	MP:0002075	abnormal coat/hair pigmentation	Krt71<em1(IMPC)Bay>/Krt71<em1(IMPC)Bay>	C57BL/6N-Krt71<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629036	M	MP:0005016	decreased lymphocyte cell number	Lelp1<em1(IMPC)Mbp>/Lelp1<em1(IMPC)Mbp>	C57BL/6NCrl-Lelp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629036	M	MP:0002606	increased basophil cell number	Lelp1<em1(IMPC)Mbp>/Lelp1<em1(IMPC)Mbp>	C57BL/6NCrl-Lelp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629036	M	MP:0005561	increased mean corpuscular hemoglobin	Lelp1<em1(IMPC)Mbp>/Lelp1<em1(IMPC)Mbp>	C57BL/6NCrl-Lelp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629036	M	MP:0000219	increased neutrophil cell number	Lelp1<em1(IMPC)Mbp>/Lelp1<em1(IMPC)Mbp>	C57BL/6NCrl-Lelp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629036	M	MP:0002590	increased mean corpuscular volume	Lelp1<em1(IMPC)Mbp>/Lelp1<em1(IMPC)Mbp>	C57BL/6NCrl-Lelp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629037	M	MP:0002135	abnormal kidney morphology	Lime1<em1(IMPC)Hmgu>/Lime1<em1(IMPC)Hmgu>	C57BL/6NCrl-Lime1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629039	F	MP:0010025	decreased total body fat amount	Lman2<em1(IMPC)Wtsi>/Lman2<em1(IMPC)Wtsi>	C57BL/6NCrl-Lman2<em1(IMPC)Wtsi>/Wtsi	N	MGI:5576271
MGI:7629040	F	MP:0001392	abnormal locomotor behavior	Lman2l<em1(IMPC)Bay>/Lman2l<+>	C57BL/6N-Lman2l<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629042	F	MP:0002092	abnormal eye morphology	Lrfn5<em1(IMPC)Tcp>/Lrfn5<em1(IMPC)Tcp>	C57BL/6NCrl-Lrfn5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629042	F	MP:0003131	increased erythrocyte cell number	Lrfn5<em1(IMPC)Tcp>/Lrfn5<em1(IMPC)Tcp>	C57BL/6NCrl-Lrfn5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629042	F	MP:0005562	decreased mean corpuscular hemoglobin	Lrfn5<em1(IMPC)Tcp>/Lrfn5<em1(IMPC)Tcp>	C57BL/6NCrl-Lrfn5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629042	F	MP:0020870	decreased thigmotaxis	Lrfn5<em1(IMPC)Tcp>/Lrfn5<em1(IMPC)Tcp>	C57BL/6NCrl-Lrfn5<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629044	M	MP:0000703	abnormal thymus morphology	Macroh2a2<em1(IMPC)Hmgu>/Macroh2a2<em1(IMPC)Hmgu>	C57BL/6NCrl-Macroh2a2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629044	M	MP:0002135	abnormal kidney morphology	Macroh2a2<em1(IMPC)Hmgu>/Macroh2a2<em1(IMPC)Hmgu>	C57BL/6NCrl-Macroh2a2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629044	M	MP:0010052	increased grip strength	Macroh2a2<em1(IMPC)Hmgu>/Macroh2a2<em1(IMPC)Hmgu>	C57BL/6NCrl-Macroh2a2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629044	M	MP:0000691	enlarged spleen	Macroh2a2<em1(IMPC)Hmgu>/Macroh2a2<em1(IMPC)Hmgu>	C57BL/6NCrl-Macroh2a2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629045	M	MP:0004738	abnormal auditory brainstem response	Mageh1<em1(IMPC)J>/Y	C57BL/6NJ-Mageh1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629046	M	MP:0005561	increased mean corpuscular hemoglobin	Marchf2<em1(IMPC)Mbp>/Marchf2<em1(IMPC)Mbp>	C57BL/6NCrl-Marchf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629046	M	MP:0005293	impaired glucose tolerance	Marchf2<em1(IMPC)Mbp>/Marchf2<em1(IMPC)Mbp>	C57BL/6NCrl-Marchf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629046	M	MP:0005564	increased hemoglobin content	Marchf2<em1(IMPC)Mbp>/Marchf2<em1(IMPC)Mbp>	C57BL/6NCrl-Marchf2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629047	M	MP:0001392	abnormal locomotor behavior	Mars1<em1(IMPC)Bay>/Mars1<+>	C57BL/6N-Mars1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629050	F	MP:0000219	increased neutrophil cell number	Mki67<em1(IMPC)Mbp>/Mki67<em1(IMPC)Mbp>	C57BL/6NCrl-Mki67<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629050	F	MP:0002060	abnormal skin morphology	Mki67<em1(IMPC)Mbp>/Mki67<em1(IMPC)Mbp>	C57BL/6NCrl-Mki67<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629050	F	MP:0000221	decreased leukocyte cell number	Mki67<em1(IMPC)Mbp>/Mki67<em1(IMPC)Mbp>	C57BL/6NCrl-Mki67<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629050	M	MP:0005011	increased eosinophil cell number	Mki67<em1(IMPC)Mbp>/Mki67<em1(IMPC)Mbp>	C57BL/6NCrl-Mki67<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629050	M	MP:0002606	increased basophil cell number	Mki67<em1(IMPC)Mbp>/Mki67<em1(IMPC)Mbp>	C57BL/6NCrl-Mki67<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629052	F	MP:0005635	decreased circulating bilirubin level	Mrpl39<em1(IMPC)J>/Mrpl39<+>	C57BL/6NJ-Mrpl39<em1(IMPC)J>/J	N	MGI:5576271
MGI:7629052	F	MP:0005554	decreased circulating creatinine level	Mrpl39<em1(IMPC)J>/Mrpl39<+>	C57BL/6NJ-Mrpl39<em1(IMPC)J>/J	N	MGI:5576271
MGI:7629053	F	MP:0003731	abnormal retina outer nuclear layer morphology	Mtcl2<em1(IMPC)Bay>/Mtcl2<em1(IMPC)Bay>	C57BL/6N-Mtcl2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629055	M	MP:0000063	decreased bone mineral density	Mybph<em1(IMPC)J>/Mybph<em1(IMPC)J>	C57BL/6NJ-Mybph<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629057	M	MP:0001510	abnormal coat appearance	Nctc1<tm1.1(NCC)WCS>/Nctc1<tm1.1(NCC)WCS>	C57BL/6N-Nctc1<tm1.1(NCC)WCS>/Wtsi	N	MGI:5576271
MGI:7629058	M	MP:0001402	decreased locomotor activity	Nfatc1<em1(IMPC)Bay>/Nfatc1<+>	C57BL/6N-Nfatc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629058	M	MP:0020870	decreased thigmotaxis	Nfatc1<em1(IMPC)Bay>/Nfatc1<+>	C57BL/6N-Nfatc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629058	M	MP:0001392	abnormal locomotor behavior	Nfatc1<em1(IMPC)Bay>/Nfatc1<+>	C57BL/6N-Nfatc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629058	M	MP:0004924	abnormal behavior	Nfatc1<em1(IMPC)Bay>/Nfatc1<+>	C57BL/6N-Nfatc1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629060	M	MP:0002757	decreased vertical activity	Nipsnap3b<em1(IMPC)J>/Nipsnap3b<em1(IMPC)J>	C57BL/6NJ-Nipsnap3b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629061	F	MP:0001297	microphthalmia	Nkiras1<em1(IMPC)Ccpcz>/Nkiras1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nkiras1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629061	F	MP:0002092	abnormal eye morphology	Nkiras1<em1(IMPC)Ccpcz>/Nkiras1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Nkiras1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629062	M	MP:0000198	decreased circulating phosphate level	Nsrp1<em1(IMPC)Mbp>/Nsrp1<+>	C57BL/6NCrl-Nsrp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629062	F	MP:0002060	abnormal skin morphology	Nsrp1<em1(IMPC)Mbp>/Nsrp1<+>	C57BL/6NCrl-Nsrp1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629065	M	MP:0001556	increased circulating HDL cholesterol level	Nudt16l1<em1(IMPC)J>/Nudt16l1<em1(IMPC)J>	C57BL/6NJ-Nudt16l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629065	M	MP:0010024	increased total body fat amount	Nudt16l1<em1(IMPC)J>/Nudt16l1<em1(IMPC)J>	C57BL/6NJ-Nudt16l1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629067	M	MP:0005635	decreased circulating bilirubin level	Nup62cl<em1(IMPC)J>/Y	C57BL/6NJ-Nup62cl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629067	M	MP:0005632	decreased circulating aspartate transaminase level	Nup62cl<em1(IMPC)J>/Y	C57BL/6NJ-Nup62cl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629067	M	MP:0000218	increased leukocyte cell number	Nup62cl<em1(IMPC)J>/Y	C57BL/6NJ-Nup62cl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629067	M	MP:0001314	cornea opacity	Nup62cl<em1(IMPC)J>/Y	C57BL/6NJ-Nup62cl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629067	M	MP:0000198	decreased circulating phosphate level	Nup62cl<em1(IMPC)J>/Y	C57BL/6NJ-Nup62cl<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629069	M	MP:0009142	decreased prepulse inhibition	Opa1<em1(IMPC)Bay>/Opa1<+>	C57BL/6N-Opa1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629070	M	MP:0003068	enlarged kidney	Paqr5<em1(IMPC)Ccpcz>/Paqr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Paqr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629070	M	MP:0002135	abnormal kidney morphology	Paqr5<em1(IMPC)Ccpcz>/Paqr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Paqr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629070	M	MP:0003917	increased kidney weight	Paqr5<em1(IMPC)Ccpcz>/Paqr5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Paqr5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629071	M	MP:0001157	small seminal vesicle	Parp1<em1(IMPC)Ccpcz>/Parp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Parp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629071	F	MP:0001120	abnormal uterus morphology	Parp1<em1(IMPC)Ccpcz>/Parp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Parp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629071	M	MP:0002059	abnormal seminal vesicle morphology	Parp1<em1(IMPC)Ccpcz>/Parp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Parp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629071	F	MP:0000689	abnormal spleen morphology	Parp1<em1(IMPC)Ccpcz>/Parp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Parp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629071	F	MP:0002092	abnormal eye morphology	Parp1<em1(IMPC)Ccpcz>/Parp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Parp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629071	F	MP:0000691	enlarged spleen	Parp1<em1(IMPC)Ccpcz>/Parp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Parp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629071	F	MP:0001297	microphthalmia	Parp1<em1(IMPC)Ccpcz>/Parp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Parp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629071	M	MP:0005553	increased circulating creatinine level	Parp1<em1(IMPC)Ccpcz>/Parp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Parp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629071	M	MP:0013279	increased fasting circulating glucose level	Parp1<em1(IMPC)Ccpcz>/Parp1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Parp1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629072	M	MP:0001303	abnormal lens morphology	Pbsn<em1(IMPC)J>/Y	C57BL/6NJ-Pbsn<em1(IMPC)J>/J	N	MGI:5576271
MGI:7629073	M	MP:0001417	decreased exploration in new environment	Pex19<em1(IMPC)Bay>/Pex19<+>	C57BL/6N-Pex19<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629074	F	MP:0000709	enlarged thymus	Pgc<em1(IMPC)Ccpcz>/Pgc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pgc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629074	M	MP:0001147	small testis	Pgc<em1(IMPC)Ccpcz>/Pgc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pgc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629074	M	MP:0009142	decreased prepulse inhibition	Pgc<em1(IMPC)Ccpcz>/Pgc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pgc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629074	M	MP:0000266	abnormal heart morphology	Pgc<em1(IMPC)Ccpcz>/Pgc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pgc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629074	M	MP:0001146	abnormal testis morphology	Pgc<em1(IMPC)Ccpcz>/Pgc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pgc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629074	F	MP:0000703	abnormal thymus morphology	Pgc<em1(IMPC)Ccpcz>/Pgc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pgc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629074	M	MP:0000274	enlarged heart	Pgc<em1(IMPC)Ccpcz>/Pgc<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pgc<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629075	M	MP:0001262	decreased body weight	Pglyrp3<em1(IMPC)Ccpcz>/Pglyrp3<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pglyrp3<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629077	F	MP:0000703	abnormal thymus morphology	Pla2g5<em1(IMPC)Ccpcz>/Pla2g5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629077	M	MP:0005343	increased circulating aspartate transaminase level	Pla2g5<em1(IMPC)Ccpcz>/Pla2g5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629077	M	MP:0000689	abnormal spleen morphology	Pla2g5<em1(IMPC)Ccpcz>/Pla2g5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629077	F	MP:0005011	increased eosinophil cell number	Pla2g5<em1(IMPC)Ccpcz>/Pla2g5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629077	F	MP:0004122	abnormal sinus arrhythmia	Pla2g5<em1(IMPC)Ccpcz>/Pla2g5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629077	F	MP:0000709	enlarged thymus	Pla2g5<em1(IMPC)Ccpcz>/Pla2g5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629077	M	MP:0002339	abnormal lymph node morphology	Pla2g5<em1(IMPC)Ccpcz>/Pla2g5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629077	M	MP:0000702	enlarged lymph nodes	Pla2g5<em1(IMPC)Ccpcz>/Pla2g5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629077	M	MP:0001146	abnormal testis morphology	Pla2g5<em1(IMPC)Ccpcz>/Pla2g5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629077	F	MP:0005385	cardiovascular system phenotype	Pla2g5<em1(IMPC)Ccpcz>/Pla2g5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629077	F	MP:0002968	increased circulating alkaline phosphatase level	Pla2g5<em1(IMPC)Ccpcz>/Pla2g5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629077	M	MP:0000691	enlarged spleen	Pla2g5<em1(IMPC)Ccpcz>/Pla2g5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629077	M	MP:0001147	small testis	Pla2g5<em1(IMPC)Ccpcz>/Pla2g5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Pla2g5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629079	M	MP:0005178	increased circulating cholesterol level	Pom121l2<em1(IMPC)J>/Pom121l2<em1(IMPC)J>	C57BL/6NJ-Pom121l2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629080	M	MP:0001891	hydrocephaly	Ppil6<em1(IMPC)Hmgu>/Ppil6<em1(IMPC)Hmgu>	C57BL/6NCrl-Ppil6<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629081	F	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number	Ppp3cb<em1(IMPC)Ccpcz>/Ppp3cb<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ppp3cb<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629081	F	MP:0008079	decreased CD8-positive, alpha-beta T cell number	Ppp3cb<em1(IMPC)Ccpcz>/Ppp3cb<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ppp3cb<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629081	F	MP:0008075	decreased CD4-positive, alpha-beta T cell number	Ppp3cb<em1(IMPC)Ccpcz>/Ppp3cb<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ppp3cb<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629081	F	MP:0013519	decreased CD4-positive NK T cell number	Ppp3cb<em1(IMPC)Ccpcz>/Ppp3cb<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ppp3cb<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629081	M	MP:0002135	abnormal kidney morphology	Ppp3cb<em1(IMPC)Ccpcz>/Ppp3cb<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ppp3cb<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629081	F	MP:0013764	decreased T-helper cell number	Ppp3cb<em1(IMPC)Ccpcz>/Ppp3cb<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ppp3cb<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629081	F	MP:0008040	decreased NK T cell number	Ppp3cb<em1(IMPC)Ccpcz>/Ppp3cb<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ppp3cb<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629081	F	MP:0013522	decreased memory-marker CD4-positive NK T cell number	Ppp3cb<em1(IMPC)Ccpcz>/Ppp3cb<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ppp3cb<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629081	F	MP:0013772	increased effector memory T-helper cell number	Ppp3cb<em1(IMPC)Ccpcz>/Ppp3cb<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ppp3cb<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629081	F	MP:0005387	immune system phenotype	Ppp3cb<em1(IMPC)Ccpcz>/Ppp3cb<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ppp3cb<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629082	F	MP:0001297	microphthalmia	Prcp<em1(IMPC)Mbp>/Prcp<em1(IMPC)Mbp>	C57BL/6NCrl-Prcp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629082	F	MP:0002092	abnormal eye morphology	Prcp<em1(IMPC)Mbp>/Prcp<em1(IMPC)Mbp>	C57BL/6NCrl-Prcp<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629083	M	MP:0001486	abnormal startle reflex	Ptgr2<em1(IMPC)Bay>/Ptgr2<em1(IMPC)Bay>	C57BL/6N-Ptgr2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629084	F	MP:0002339	abnormal lymph node morphology	Ptprz1<em1(IMPC)Ccpcz>/Ptprz1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ptprz1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629084	F	MP:0002092	abnormal eye morphology	Ptprz1<em1(IMPC)Ccpcz>/Ptprz1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ptprz1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629084	M	MP:0002060	abnormal skin morphology	Ptprz1<em1(IMPC)Ccpcz>/Ptprz1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ptprz1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629084	M	MP:0001199	thin skin	Ptprz1<em1(IMPC)Ccpcz>/Ptprz1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ptprz1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629084	F	MP:0000689	abnormal spleen morphology	Ptprz1<em1(IMPC)Ccpcz>/Ptprz1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ptprz1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629084	F	MP:0000691	enlarged spleen	Ptprz1<em1(IMPC)Ccpcz>/Ptprz1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ptprz1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629084	F	MP:0000702	enlarged lymph nodes	Ptprz1<em1(IMPC)Ccpcz>/Ptprz1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ptprz1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629084	F	MP:0001293	anophthalmia	Ptprz1<em1(IMPC)Ccpcz>/Ptprz1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Ptprz1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629087	M	MP:0001523	impaired righting response	Rnf217<em1(IMPC)J>/Rnf217<em1(IMPC)J>	C57BL/6NJ-Rnf217<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629090	F	MP:0001392	abnormal locomotor behavior	Scart1<em1(IMPC)Bay>/Scart1<em1(IMPC)Bay>	C57BL/6N-Scart1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629093	M	MP:0001529	abnormal vocalization	Sec62<em1(IMPC)J>/Sec62<+>	C57BL/6NJ-Sec62<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629095	M	MP:0002075	abnormal coat/hair pigmentation	Sis<em1(IMPC)J>/Sis<em1(IMPC)J>	C57BL/6NJ-Sis<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629096	M	MP:0000689	abnormal spleen morphology	Skic8<em1(IMPC)Tcp>/Skic8<+>	C57BL/6NCrl-Skic8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629096	M	MP:0000702	enlarged lymph nodes	Skic8<em1(IMPC)Tcp>/Skic8<+>	C57BL/6NCrl-Skic8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629098	F	MP:0001402	decreased locomotor activity	Ski<em1(IMPC)Bay>/Ski<+>	C57BL/6N-Ski<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629098	M	MP:0001513	limb grasping	Ski<em1(IMPC)Bay>/Ski<+>	C57BL/6N-Ski<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629099	M	MP:0000702	enlarged lymph nodes	Slc22a7<em1(IMPC)Tcp>/Slc22a7<em1(IMPC)Tcp>	C57BL/6NCrl-Slc22a7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629099	M	MP:0002060	abnormal skin morphology	Slc22a7<em1(IMPC)Tcp>/Slc22a7<em1(IMPC)Tcp>	C57BL/6NCrl-Slc22a7<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629101	M	MP:0001406	abnormal gait	Slc26a11<em1(IMPC)Mbp>/Slc26a11<em1(IMPC)Mbp>	C57BL/6NCrl-Slc26a11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629101	M	MP:0001364	decreased anxiety-related response	Slc26a11<em1(IMPC)Mbp>/Slc26a11<em1(IMPC)Mbp>	C57BL/6NCrl-Slc26a11<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629102	M	MP:0001392	abnormal locomotor behavior	Slc35a3<em1(IMPC)Bay>/Slc35a3<+>	C57BL/6N-Slc35a3<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629103	F	MP:0001289	persistence of hyaloid vascular system	Slc6a20b<em1(IMPC)J>/Slc6a20b<em1(IMPC)J>	C57BL/6NJ-Slc6a20b<em1(IMPC)J>/J	N	MGI:5576271
MGI:7629103	F	MP:0000367	abnormal coat/ hair morphology	Slc6a20b<em1(IMPC)J>/Slc6a20b<em1(IMPC)J>	C57BL/6NJ-Slc6a20b<em1(IMPC)J>/J	N	MGI:5576271
MGI:7629103	F	MP:0005566	decreased blood urea nitrogen level	Slc6a20b<em1(IMPC)J>/Slc6a20b<em1(IMPC)J>	C57BL/6NJ-Slc6a20b<em1(IMPC)J>/J	N	MGI:5576271
MGI:7629103	F	MP:0002833	increased heart weight	Slc6a20b<em1(IMPC)J>/Slc6a20b<em1(IMPC)J>	C57BL/6NJ-Slc6a20b<em1(IMPC)J>/J	N	MGI:5576271
MGI:7629103	F	MP:0005544	cornea deposits	Slc6a20b<em1(IMPC)J>/Slc6a20b<em1(IMPC)J>	C57BL/6NJ-Slc6a20b<em1(IMPC)J>/J	N	MGI:5576271
MGI:7629104	F	MP:0001529	abnormal vocalization	Snx33<em1(IMPC)J>/Snx33<em1(IMPC)J>	C57BL/6NJ-Snx33<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629112	F	MP:0020421	increased freezing behavior	Swsap1<em1(IMPC)Mbp>/Swsap1<em1(IMPC)Mbp>	C57BL/6NCrl-Swsap1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629112	M	MP:0001146	abnormal testis morphology	Swsap1<em1(IMPC)Mbp>/Swsap1<em1(IMPC)Mbp>	C57BL/6NCrl-Swsap1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629112	M	MP:0001147	small testis	Swsap1<em1(IMPC)Mbp>/Swsap1<em1(IMPC)Mbp>	C57BL/6NCrl-Swsap1<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629113	F	MP:0005505	thrombocytosis	Syngr2<em1(IMPC)J>/Syngr2<em1(IMPC)J>	C57BL/6NJ-Syngr2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629113	M	MP:0005559	increased circulating glucose level	Syngr2<em1(IMPC)J>/Syngr2<em1(IMPC)J>	C57BL/6NJ-Syngr2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629113	F	MP:0001284	absent vibrissae	Syngr2<em1(IMPC)J>/Syngr2<em1(IMPC)J>	C57BL/6NJ-Syngr2<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629114	M	MP:0001510	abnormal coat appearance	Tcp11x2<em1(IMPC)Hmgu>/Y	C57BL/6NCrl-Tcp11x2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629115	F	MP:0001417	decreased exploration in new environment	Tex36<em1(IMPC)J>/Tex36<em1(IMPC)J>	C57BL/6NJ-Tex36<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629116	M	MP:0009142	decreased prepulse inhibition	Thtpa<em1(IMPC)Tcp>/Thtpa<em1(IMPC)Tcp>	C57BL/6NCrl-Thtpa<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629117	M	MP:0005635	decreased circulating bilirubin level	Timm17b<em1(IMPC)J>/Y	C57BL/6NJ-Timm17b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629118	F	MP:0005505	thrombocytosis	Timm17b<em1(IMPC)J>/Timm17b<em1(IMPC)J>	C57BL/6NJ-Timm17b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629118	F	MP:0005635	decreased circulating bilirubin level	Timm17b<em1(IMPC)J>/Timm17b<em1(IMPC)J>	C57BL/6NJ-Timm17b<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629119	M	MP:0010024	increased total body fat amount	Tm9sf1<em1(IMPC)Bay>/Tm9sf1<em1(IMPC)Bay>	C57BL/6N-Tm9sf1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629120	F	MP:0008259	abnormal optic disk morphology	Tmeff2<em1(IMPC)Hmgu>/Tmeff2<+>	C57BL/6NCrl-Tmeff2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629120	M	MP:0001325	abnormal retina morphology	Tmeff2<em1(IMPC)Hmgu>/Tmeff2<+>	C57BL/6NCrl-Tmeff2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629120	M	MP:0002699	abnormal vitreous body morphology	Tmeff2<em1(IMPC)Hmgu>/Tmeff2<+>	C57BL/6NCrl-Tmeff2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629120	M	MP:0005554	decreased circulating creatinine level	Tmeff2<em1(IMPC)Hmgu>/Tmeff2<+>	C57BL/6NCrl-Tmeff2<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629123	M	MP:0001914	hemorrhage	Tmem17<em1(IMPC)Kmpc>/Tmem17<em1(IMPC)Kmpc>	C57BL/6NTac-Tmem17<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7629124	F	MP:0002764	short tibia	Tmem88<em1(IMPC)Kmpc>/Tmem88<em1(IMPC)Kmpc>	C57BL/6NTac-Tmem88<em1(IMPC)Kmpc>/Kmpc	N	MGI:5576271
MGI:7629125	M	MP:0000556	abnormal hindlimb morphology	Tmlhe<em1(IMPC)Bay>/Y	C57BL/6N-Tmlhe<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629125	M	MP:0001406	abnormal gait	Tmlhe<em1(IMPC)Bay>/Y	C57BL/6N-Tmlhe<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629125	M	MP:0000443	abnormal snout morphology	Tmlhe<em1(IMPC)Bay>/Y	C57BL/6N-Tmlhe<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629126	M	MP:0001925	male infertility	Tmprss12<em1(IMPC)Mbp>/Tmprss12<em1(IMPC)Mbp>	C57BL/6NCrl-Tmprss12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629126	F	MP:0002092	abnormal eye morphology	Tmprss12<em1(IMPC)Mbp>/Tmprss12<em1(IMPC)Mbp>	C57BL/6NCrl-Tmprss12<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629127	M	MP:0001529	abnormal vocalization	Tnrc6c<em1(IMPC)J>/Tnrc6c<em1(IMPC)J>	C57BL/6NJ-Tnrc6c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629127	M	MP:0002075	abnormal coat/hair pigmentation	Tnrc6c<em1(IMPC)J>/Tnrc6c<em1(IMPC)J>	C57BL/6NJ-Tnrc6c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629129	F	MP:0002606	increased basophil cell number	Tor1b<em1(IMPC)Mbp>/Tor1b<em1(IMPC)Mbp>	C57BL/6NCrl-Tor1b<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629130	M	MP:0005011	increased eosinophil cell number	Trappc8<em1(IMPC)Tcp>/Trappc8<+>	C57BL/6NCrl-Trappc8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629130	F	MP:0010097	abnormal retina blood vessel morphology	Trappc8<em1(IMPC)Tcp>/Trappc8<+>	C57BL/6NCrl-Trappc8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629130	M	MP:0001944	abnormal pancreas morphology	Trappc8<em1(IMPC)Tcp>/Trappc8<+>	C57BL/6NCrl-Trappc8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629130	M	MP:0002941	increased circulating alanine transaminase level	Trappc8<em1(IMPC)Tcp>/Trappc8<+>	C57BL/6NCrl-Trappc8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629130	F	MP:0000220	increased monocyte cell number	Trappc8<em1(IMPC)Tcp>/Trappc8<+>	C57BL/6NCrl-Trappc8<em1(IMPC)Tcp>/Tcp	N	MGI:5576271
MGI:7629132	M	MP:0010024	increased total body fat amount	Trim10<em1(IMPC)J>/Trim10<em1(IMPC)J>	C57BL/6NJ-Trim10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629132	F	MP:0002590	increased mean corpuscular volume	Trim10<em1(IMPC)J>/Trim10<em1(IMPC)J>	C57BL/6NJ-Trim10<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629133	F	MP:0002092	abnormal eye morphology	Tsnax<em1(IMPC)Mbp>/Tsnax<em1(IMPC)Mbp>	C57BL/6NCrl-Tsnax<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629133	M	MP:0001944	abnormal pancreas morphology	Tsnax<em1(IMPC)Mbp>/Tsnax<em1(IMPC)Mbp>	C57BL/6NCrl-Tsnax<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629134	M	MP:0001925	male infertility	Tssk2<em1(IMPC)Mbp>/Tssk2<em1(IMPC)Mbp>	C57BL/6NCrl-Tssk2<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629135	M	MP:0005293	impaired glucose tolerance	Ttc38<em1Llp>/Ttc38<em1Llp>	C57BL/6NJ-Ttc38<em1Llp>/J	N	MGI:5576271
MGI:7629136	M	MP:0000063	decreased bone mineral density	Ttc39c<em1(IMPC)J>/Ttc39c<em1(IMPC)J>	C57BL/6NJ-Ttc39c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629136	M	MP:0010024	increased total body fat amount	Ttc39c<em1(IMPC)J>/Ttc39c<em1(IMPC)J>	C57BL/6NJ-Ttc39c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629136	M	MP:0002608	increased hematocrit	Ttc39c<em1(IMPC)J>/Ttc39c<em1(IMPC)J>	C57BL/6NJ-Ttc39c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629137	M	MP:0000186	decreased circulating HDL cholesterol level	Tti1<em1(IMPC)J>/Tti1<+>	C57BL/6NJ-Tti1<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629139	M	MP:0011110	preweaning lethality, incomplete penetrance	Ttyh1<em1(IMPC)Bay>/Ttyh1<em1(IMPC)Bay>	C57BL/6N-Ttyh1<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629140	M	MP:0001399	hyperactivity	Tube1<em1(IMPC)Hmgu>/Tube1<+>	C57BL/6NCrl-Tube1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629140	M	MP:0020870	decreased thigmotaxis	Tube1<em1(IMPC)Hmgu>/Tube1<+>	C57BL/6NCrl-Tube1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629140	M	MP:0001364	decreased anxiety-related response	Tube1<em1(IMPC)Hmgu>/Tube1<+>	C57BL/6NCrl-Tube1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629140	M	MP:0004924	abnormal behavior	Tube1<em1(IMPC)Hmgu>/Tube1<+>	C57BL/6NCrl-Tube1<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629142	F	MP:0002764	short tibia	Vdr<em1(IMPC)Hmgu>/Vdr<em1(IMPC)Hmgu>	C57BL/6NCrl-Vdr<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629142	F	MP:0000745	tremors	Vdr<em1(IMPC)Hmgu>/Vdr<em1(IMPC)Hmgu>	C57BL/6NCrl-Vdr<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629142	M	MP:0001489	decreased startle reflex	Vdr<em1(IMPC)Hmgu>/Vdr<em1(IMPC)Hmgu>	C57BL/6NCrl-Vdr<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629143	M	MP:0001510	abnormal coat appearance	Vstm4<em1(IMPC)J>/Vstm4<em1(IMPC)J>	C57BL/6NJ-Vstm4<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629144	M	MP:0002135	abnormal kidney morphology	Vstm5<em1(IMPC)Hmgu>/Vstm5<em1(IMPC)Hmgu>	C57BL/6NCrl-Vstm5<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629145	M	MP:0003020	decreased circulating chloride level	Vsx1<em1(IMPC)Ccpcz>/Vsx1<em1(IMPC)Ccpcz>	C57BL/6NCrl-Vsx1<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	M	MP:0010052	increased grip strength	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	M	MP:0000161	scoliosis	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	M	MP:0000280	thin ventricular wall	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	M	MP:0000438	abnormal cranium morphology	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	M	MP:0001402	decreased locomotor activity	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	F	MP:0001552	increased circulating triglyceride level	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	F	MP:0001325	abnormal retina morphology	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	F	MP:0001926	female infertility	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	M	MP:0001925	male infertility	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	M	MP:0001147	small testis	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	M	MP:0001146	abnormal testis morphology	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	M	MP:0002797	increased thigmotaxis	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	M	MP:0001417	decreased exploration in new environment	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	F	MP:0003917	increased kidney weight	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	M	MP:0004599	abnormal vertebral arch morphology	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	F	MP:0002968	increased circulating alkaline phosphatase level	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629146	F	MP:0003921	abnormal heart left ventricle morphology	Xrcc5<em1(IMPC)Ccpcz>/Xrcc5<em1(IMPC)Ccpcz>	C57BL/6NCrl-Xrcc5<em1(IMPC)Ccpcz>/Ccpcz	N	MGI:5576271
MGI:7629147	F	MP:0009709	hydrometra	Zbed3<em1(IMPC)Mbp>/Zbed3<em1(IMPC)Mbp>	C57BL/6NCrl-Zbed3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629147	F	MP:0002092	abnormal eye morphology	Zbed3<em1(IMPC)Mbp>/Zbed3<em1(IMPC)Mbp>	C57BL/6NCrl-Zbed3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629147	F	MP:0001297	microphthalmia	Zbed3<em1(IMPC)Mbp>/Zbed3<em1(IMPC)Mbp>	C57BL/6NCrl-Zbed3<em1(IMPC)Mbp>/MbpMmucd	N	MGI:5576271
MGI:7629148	F	MP:0001415	increased exploration in new environment	Zfp280c<em1(IMPC)Hmgu>/Zfp280c<em1(IMPC)Hmgu>	C57BL/6NCrl-Zfp280c<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629148	F	MP:0001392	abnormal locomotor behavior	Zfp280c<em1(IMPC)Hmgu>/Zfp280c<em1(IMPC)Hmgu>	C57BL/6NCrl-Zfp280c<em1(IMPC)Hmgu>/Ieg	N	MGI:5576271
MGI:7629149	M	MP:0002102	abnormal ear morphology	Zfp385c<em1(IMPC)J>/Zfp385c<em1(IMPC)J>	C57BL/6NJ-Zfp385c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629149	M	MP:0010024	increased total body fat amount	Zfp385c<em1(IMPC)J>/Zfp385c<em1(IMPC)J>	C57BL/6NJ-Zfp385c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629149	M	MP:0003961	decreased lean body mass	Zfp385c<em1(IMPC)J>/Zfp385c<em1(IMPC)J>	C57BL/6NJ-Zfp385c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629149	M	MP:0011110	preweaning lethality, incomplete penetrance	Zfp385c<em1(IMPC)J>/Zfp385c<em1(IMPC)J>	C57BL/6NJ-Zfp385c<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629150	F	MP:0005632	decreased circulating aspartate transaminase level	Zfp551<em1(IMPC)J>/Zfp551<em1(IMPC)J>	C57BL/6NJ-Zfp551<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629150	F	MP:0005554	decreased circulating creatinine level	Zfp551<em1(IMPC)J>/Zfp551<em1(IMPC)J>	C57BL/6NJ-Zfp551<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629150	F	MP:0005635	decreased circulating bilirubin level	Zfp551<em1(IMPC)J>/Zfp551<em1(IMPC)J>	C57BL/6NJ-Zfp551<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629151	M	MP:0002644	decreased circulating triglyceride level	Zfp697<em1(IMPC)J>/Zfp697<em1(IMPC)J>	C57BL/6NJ-Zfp697<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629152	F	MP:0001402	decreased locomotor activity	Zfr2<em1(IMPC)Bay>/Zfr2<em1(IMPC)Bay>	C57BL/6N-Zfr2<em1(IMPC)Bay>/BayMmucd	N	MGI:5576271
MGI:7629153	F	MP:0005632	decreased circulating aspartate transaminase level	Zmynd12<em1(IMPC)J>/Zmynd12<em1(IMPC)J>	C57BL/6NJ-Zmynd12<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629153	F	MP:0005505	thrombocytosis	Zmynd12<em1(IMPC)J>/Zmynd12<em1(IMPC)J>	C57BL/6NJ-Zmynd12<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629153	F	MP:0005635	decreased circulating bilirubin level	Zmynd12<em1(IMPC)J>/Zmynd12<em1(IMPC)J>	C57BL/6NJ-Zmynd12<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629153	M	MP:0003961	decreased lean body mass	Zmynd12<em1(IMPC)J>/Zmynd12<em1(IMPC)J>	C57BL/6NJ-Zmynd12<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629153	F	MP:0002942	decreased circulating alanine transaminase level	Zmynd12<em1(IMPC)J>/Zmynd12<em1(IMPC)J>	C57BL/6NJ-Zmynd12<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7629153	M	MP:0010024	increased total body fat amount	Zmynd12<em1(IMPC)J>/Zmynd12<em1(IMPC)J>	C57BL/6NJ-Zmynd12<em1(IMPC)J>/Mmjax	N	MGI:5576271
MGI:7638773	M	MP:0009230	abnormal sperm head morphology	Cylc1<em1Chnsr>/Y	involves: C57BL/6JGpt	N	38573307
MGI:7638773	M	MP:0004542	impaired acrosome reaction	Cylc1<em1Chnsr>/Y	involves: C57BL/6JGpt	N	38573307
MGI:7638773	M	MP:0005389	reproductive system phenotype	Cylc1<em1Chnsr>/Y	involves: C57BL/6JGpt	Y	38573307
MGI:7638773	M	MP:0001922	reduced male fertility	Cylc1<em1Chnsr>/Y	involves: C57BL/6JGpt	N	38573307
MGI:7638773	M	MP:0009231	detached acrosome	Cylc1<em1Chnsr>/Y	involves: C57BL/6JGpt	N	38573307
MGI:7638773	M	MP:0009647	decreased fertilization frequency	Cylc1<em1Chnsr>/Y	involves: C57BL/6JGpt	N	38573307
MGI:7638774	M	MP:0009231	detached acrosome	Cylc1<em2Chnsr>/Y	involves: C57BL/6JGpt	N	38573307
MGI:7638774	M	MP:0001922	reduced male fertility	Cylc1<em2Chnsr>/Y	involves: C57BL/6JGpt	N	38573307
MGI:7638774	M	MP:0009230	abnormal sperm head morphology	Cylc1<em2Chnsr>/Y	involves: C57BL/6JGpt	N	38573307
MGI:7638774	M	MP:0005389	reproductive system phenotype	Cylc1<em2Chnsr>/Y	involves: C57BL/6JGpt	N	38573307
MGI:7639693	F	MP:0001935	decreased litter size	Canx<tm1.1Osb>/Canx<tm1.1Osb>	involves: 129S2/SvPas	N	26388295
MGI:7639693	M	MP:0004852	decreased testis weight	Canx<tm1.1Osb>/Canx<tm1.1Osb>	involves: 129S2/SvPas	N	26388295
MGI:7639693	M	MP:0001147	small testis	Canx<tm1.1Osb>/Canx<tm1.1Osb>	involves: 129S2/SvPas	N	26388295
MGI:7639695	F	MP:0005389	reproductive system phenotype	Canx<tm1.2Osb>/Canx<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	Y	26388295
MGI:7639696	M	MP:0005389	reproductive system phenotype	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Stra8-cre)1Osb/0	involves: 129S2/SvPas	Y	26388295
MGI:7639697	F	MP:0001125	abnormal oocyte morphology	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	26388295
MGI:7639697	F	MP:0001129	impaired ovarian folliculogenesis	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	26388295
MGI:7639697	F	MP:0009647	decreased fertilization frequency	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	26388295
MGI:7639697	F	MP:0002682	decreased mature ovarian follicle number	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	26388295
MGI:7639697	F	MP:0004856	decreased ovary weight	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	26388295
MGI:7639697	F	MP:0031420	decreased superovulation rate	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	26388295
MGI:7639697	F	MP:0002680	decreased corpora lutea number	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	26388295
MGI:7639697	F	MP:0011128	increased tertiary ovarian follicle number	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	26388295
MGI:7639697	F	MP:0031018	decreased granulosa cell proliferation	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	26388295
MGI:7639697	F	MP:0001131	abnormal ovarian follicle morphology	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	26388295
MGI:7639697	F	MP:0001935	decreased litter size	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	26388295
MGI:7639697	F	MP:0001923	reduced female fertility	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	26388295
MGI:7639697	F	MP:0011701	decreased cumulus expansion	Calr<tm1.2Osb>/Calr<tm1.1Osb>,Tg(Zp3-cre)93Knw/0	involves: 129S2/SvPas * C57BL/6J	N	26388295
MGI:7639751	M	MP:0005389	reproductive system phenotype	Cdh2<tm1.1Ayki>/Cdh2<tm1.1Ayki>	involves: C57BL/6 * DBA/2	Y	33494786
MGI:7639751	M	MP:0020551	abnormal postsynaptic density morphology	Cdh2<tm1.1Ayki>/Cdh2<tm1.1Ayki>	involves: C57BL/6 * DBA/2	N	33494786
MGI:7639751	M	MP:0009455	enhanced cued conditioning behavior	Cdh2<tm1.1Ayki>/Cdh2<tm1.1Ayki>	involves: C57BL/6 * DBA/2	N	33494786
MGI:7639751	M	MP:0003008	enhanced long-term potentiation	Cdh2<tm1.1Ayki>/Cdh2<tm1.1Ayki>	involves: C57BL/6 * DBA/2	N	33494786
MGI:7639751	M	MP:0002912	abnormal excitatory postsynaptic potential	Cdh2<tm1.1Ayki>/Cdh2<tm1.1Ayki>	involves: C57BL/6 * DBA/2	N	33494786
MGI:7639751	M	MP:0020360	abnormal asymmetric synapse morphology	Cdh2<tm1.1Ayki>/Cdh2<tm1.1Ayki>	involves: C57BL/6 * DBA/2	N	33494786
MGI:7639751	M	MP:0002206	abnormal CNS synaptic transmission	Cdh2<tm1.1Ayki>/Cdh2<tm1.1Ayki>	involves: C57BL/6 * DBA/2	N	33494786
MGI:7639751	M	MP:0005378	growth/size/body region phenotype	Cdh2<tm1.1Ayki>/Cdh2<tm1.1Ayki>	involves: C57BL/6 * DBA/2	Y	33494786
MGI:7639751	M	MP:0009940	abnormal hippocampus pyramidal cell morphology	Cdh2<tm1.1Ayki>/Cdh2<tm1.1Ayki>	involves: C57BL/6 * DBA/2	N	33494786
MGI:7639751	M	MP:0003631	nervous system phenotype	Cdh2<tm1.1Ayki>/Cdh2<tm1.1Ayki>	involves: C57BL/6 * DBA/2	Y	33494786
MGI:7639751	M	MP:0014369	enhanced spatial working memory	Cdh2<tm1.1Ayki>/Cdh2<tm1.1Ayki>	involves: C57BL/6 * DBA/2	N	33494786
MGI:7639837	F	MP:0000609	abnormal liver physiology	Gramd1c<tm1a(KOMP)Wtsi>/Gramd1c<tm1a(KOMP)Wtsi>	C57BL/6N-A<tm1Brd> Gramd1c<tm1a(KOMP)Wtsi>/JMmucd	N	38694206
MGI:7639837	F	MP:0013275	abnormal xenobiotic metabolism	Gramd1c<tm1a(KOMP)Wtsi>/Gramd1c<tm1a(KOMP)Wtsi>	C57BL/6N-A<tm1Brd> Gramd1c<tm1a(KOMP)Wtsi>/JMmucd	N	38694206
MGI:7639837	F	MP:0012338	decreased bile salt level	Gramd1c<tm1a(KOMP)Wtsi>/Gramd1c<tm1a(KOMP)Wtsi>	C57BL/6N-A<tm1Brd> Gramd1c<tm1a(KOMP)Wtsi>/JMmucd	N	38694206
MGI:7639837	F	MP:0005378	growth/size/body region phenotype	Gramd1c<tm1a(KOMP)Wtsi>/Gramd1c<tm1a(KOMP)Wtsi>	C57BL/6N-A<tm1Brd> Gramd1c<tm1a(KOMP)Wtsi>/JMmucd	Y	38694206
MGI:7639837	M	MP:0002665	decreased circulating corticosterone level	Gramd1c<tm1a(KOMP)Wtsi>/Gramd1c<tm1a(KOMP)Wtsi>	C57BL/6N-A<tm1Brd> Gramd1c<tm1a(KOMP)Wtsi>/JMmucd	N	38694206
MGI:7639837	F	MP:0010027	increased liver cholesterol level	Gramd1c<tm1a(KOMP)Wtsi>/Gramd1c<tm1a(KOMP)Wtsi>	C57BL/6N-A<tm1Brd> Gramd1c<tm1a(KOMP)Wtsi>/JMmucd	N	38694206
MGI:7639837	F	MP:0009355	increased liver triglyceride level	Gramd1c<tm1a(KOMP)Wtsi>/Gramd1c<tm1a(KOMP)Wtsi>	C57BL/6N-A<tm1Brd> Gramd1c<tm1a(KOMP)Wtsi>/JMmucd	N	38694206
MGI:7639945	M	MP:0002675	asthenozoospermia	Itpripl1<em1Smoc>/Itpripl1<em1Smoc>	C57BL/6J-Itpripl1<em1Smoc>	N	38614099
MGI:7639945	M	MP:0001146	abnormal testis morphology	Itpripl1<em1Smoc>/Itpripl1<em1Smoc>	C57BL/6J-Itpripl1<em1Smoc>	N	38614099
MGI:7640124	M	MP:0002942	decreased circulating alanine transaminase level	Ms4a7<em1.1Jddl>/Ms4a7<em1.1Jddl>	B6.Cg-Ms4a7<em1.1Jddl>	N	38478630
MGI:7640124	M	MP:0008658	decreased interleukin-1 beta secretion	Ms4a7<em1.1Jddl>/Ms4a7<em1.1Jddl>	B6.Cg-Ms4a7<em1.1Jddl>	N	38478630
MGI:7640124	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Ms4a7<em1.1Jddl>/Ms4a7<em1.1Jddl>	B6.Cg-Ms4a7<em1.1Jddl>	N	38478630
MGI:7640124	M	MP:0008554	decreased circulating tumor necrosis factor level	Ms4a7<em1.1Jddl>/Ms4a7<em1.1Jddl>	B6.Cg-Ms4a7<em1.1Jddl>	N	38478630
MGI:7640124	M	MP:0000598	abnormal liver morphology	Ms4a7<em1.1Jddl>/Ms4a7<em1.1Jddl>	B6.Cg-Ms4a7<em1.1Jddl>	N	38478630
MGI:7640124	M	MP:0004808	abnormal hematopoietic stem cell morphology	Ms4a7<em1.1Jddl>/Ms4a7<em1.1Jddl>	B6.Cg-Ms4a7<em1.1Jddl>	N	38478630
MGI:7640124	M	MP:0008891	decreased hepatocyte apoptosis	Ms4a7<em1.1Jddl>/Ms4a7<em1.1Jddl>	B6.Cg-Ms4a7<em1.1Jddl>	N	38478630
MGI:7640124	M	MP:0003884	decreased macrophage cell number	Ms4a7<em1.1Jddl>/Ms4a7<em1.1Jddl>	B6.Cg-Ms4a7<em1.1Jddl>	N	38478630
MGI:7640124	M	MP:0005632	decreased circulating aspartate transaminase level	Ms4a7<em1.1Jddl>/Ms4a7<em1.1Jddl>	B6.Cg-Ms4a7<em1.1Jddl>	N	38478630
MGI:7640124	M	MP:0014434	decreased cytokine level	Ms4a7<em1.1Jddl>/Ms4a7<em1.1Jddl>	B6.Cg-Ms4a7<em1.1Jddl>	N	38478630
MGI:7640124	M	MP:0002451	abnormal macrophage physiology	Ms4a7<em1.1Jddl>/Ms4a7<em1.1Jddl>	B6.Cg-Ms4a7<em1.1Jddl>	N	38478630
MGI:7640137	M	MP:0002942	decreased circulating alanine transaminase level	Ms4a7<em1Jddl>/Ms4a7<em1Jddl>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	B6.Cg-Lyz2<tm1(cre)Ifo> Ms4a7<em1Jddl>	N	38478630
MGI:7640137	M	MP:0000598	abnormal liver morphology	Ms4a7<em1Jddl>/Ms4a7<em1Jddl>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	B6.Cg-Lyz2<tm1(cre)Ifo> Ms4a7<em1Jddl>	N	38478630
MGI:7640137	M	MP:0014434	decreased cytokine level	Ms4a7<em1Jddl>/Ms4a7<em1Jddl>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	B6.Cg-Lyz2<tm1(cre)Ifo> Ms4a7<em1Jddl>	N	38478630
MGI:7640137	M	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis	Ms4a7<em1Jddl>/Ms4a7<em1Jddl>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	B6.Cg-Lyz2<tm1(cre)Ifo> Ms4a7<em1Jddl>	N	38478630
MGI:7640137	M	MP:0005632	decreased circulating aspartate transaminase level	Ms4a7<em1Jddl>/Ms4a7<em1Jddl>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	B6.Cg-Lyz2<tm1(cre)Ifo> Ms4a7<em1Jddl>	N	38478630
MGI:7640137	M	MP:0008554	decreased circulating tumor necrosis factor level	Ms4a7<em1Jddl>/Ms4a7<em1Jddl>,Lyz2<tm1(cre)Ifo>/Lyz2<+>	B6.Cg-Lyz2<tm1(cre)Ifo> Ms4a7<em1Jddl>	N	38478630
MGI:7640139	M	MP:0005159	azoospermia	Exoc7<em1Utr>/Exoc7<em1Utr>,Nanos3<tm2.1(cre)Ysa>/Nanos3<+>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	38325858
MGI:7640139	M	MP:0006379	abnormal spermatocyte morphology	Exoc7<em1Utr>/Exoc7<em1Utr>,Nanos3<tm2.1(cre)Ysa>/Nanos3<+>	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	N	38325858
MGI:7640171	M	MP:0005169	abnormal male meiosis	Kctd19<em1Fcw>/Kctd19<em1Fcw>	Not Specified	N	35341968
MGI:7640171	M	MP:0014052	increased male germ cell apoptosis	Kctd19<em1Fcw>/Kctd19<em1Fcw>	Not Specified	N	35341968
MGI:7640171	M	MP:0005159	azoospermia	Kctd19<em1Fcw>/Kctd19<em1Fcw>	Not Specified	N	35341968
MGI:7640171	M	MP:0001925	male infertility	Kctd19<em1Fcw>/Kctd19<em1Fcw>	Not Specified	N	35341968
MGI:7640171	M	MP:0001156	abnormal spermatogenesis	Kctd19<em1Fcw>/Kctd19<em1Fcw>	Not Specified	N	35341968
MGI:7641564	F	MP:0031020	premature ovarian failure	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	M	MP:0009451	abnormal chromosomal synapsis	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	F	MP:0005431	decreased oocyte number	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	M	MP:0005169	abnormal male meiosis	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	F	MP:0001926	female infertility	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	M	MP:0001153	small seminiferous tubules	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	M	MP:0002216	abnormal seminiferous tubule morphology	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	M	MP:0008261	arrest of male meiosis	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	M	MP:0001925	male infertility	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	M	MP:0001147	small testis	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	M	MP:0004901	decreased male germ cell number	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	F	MP:0004805	absent oocytes	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	F	MP:0005168	abnormal female meiosis	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	M	MP:0001155	arrest of spermatogenesis	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	M	MP:0004852	decreased testis weight	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	M	MP:0009452	abnormal synaptonemal complex	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	M	MP:0005159	azoospermia	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	F	MP:0001127	small ovary	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	F	MP:0013236	ovary degeneration	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641564	M	MP:0014052	increased male germ cell apoptosis	Firrm<em1Gpt>/Firrm<em1Gpt>,Stra8<em1(GFP/cre)Smoc>/Stra8<+>	involves: C57BL/6JGpt	N	37439366
MGI:7641771	M	MP:0009732	ventricular premature beat	Kcne5<tm1Lex>/Y	involves: 129S/SvEv * C57BL/6	N	30289750
MGI:7641771	M	MP:0020345	abnormal myocardial fiber currents	Kcne5<tm1Lex>/Y	involves: 129S/SvEv * C57BL/6	N	30289750
MGI:7641771	M	MP:0001544	abnormal cardiovascular system physiology	Kcne5<tm1Lex>/Y	involves: 129S/SvEv * C57BL/6	N	30289750
MGI:7641771	M	MP:0008950	ventricular tachycardia	Kcne5<tm1Lex>/Y	involves: 129S/SvEv * C57BL/6	N	30289750
MGI:7641773	M	MP:0020345	abnormal myocardial fiber currents	Kcne5<em1Mdcb>/Y	C57BL/6NCrl-Kcne5<em1Mdcb>	N	30289750
MGI:7641773	M	MP:0009732	ventricular premature beat	Kcne5<em1Mdcb>/Y	C57BL/6NCrl-Kcne5<em1Mdcb>	N	30289750
MGI:7641773	M	MP:0008950	ventricular tachycardia	Kcne5<em1Mdcb>/Y	C57BL/6NCrl-Kcne5<em1Mdcb>	N	30289750
MGI:7643182	F	MP:0005389	reproductive system phenotype	D930020B18Rik<em1Osb>/D930020B18Rik<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	38786026
MGI:7643184	F	MP:0005389	reproductive system phenotype	Elobl<em1Osb>/Elobl<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38786026
MGI:7643185	F	MP:0005389	reproductive system phenotype	Fbxw15<em1Osb>/Fbxw15<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38786026
MGI:7643186	F	MP:0005389	reproductive system phenotype	Mix23<em1Osb>/Mix23<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38786026
MGI:7643187	F	MP:0005389	reproductive system phenotype	Nlrp2<em1Kzt>/Nlrp2<em1Kzt>	involves: C57BL/6NJcl * DBA/2NJcl	N	38786026
MGI:7643188	F	MP:0005389	reproductive system phenotype	Oas1h<em1Osb>/Oas1h<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38786026
MGI:7643189	F	MP:0005389	reproductive system phenotype	Pkd1l2<em1Osb>/Pkd1l2<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38786026
MGI:7643190	F	MP:0005389	reproductive system phenotype	Pramel34<em1Kzt>/Pramel34<em1Kzt>	involves: C57BL/6NJcl * DBA/2NJcl	N	38786026
MGI:7643191	F	MP:0005389	reproductive system phenotype	Pramel47<em1Kzt>/Pramel47<em1Kzt>	involves: C57BL/6NJcl * DBA/2NJcl	N	38786026
MGI:7643192	F	MP:0005389	reproductive system phenotype	Sting1<em1Osb>/Sting1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38786026
MGI:7643193	F	MP:0005389	reproductive system phenotype	Tspan4<em1Osb>/Tspan4<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38786026
MGI:7643194	F	MP:0005389	reproductive system phenotype	Tubal3<em1Kzt>/Tubal3<em1Kzt>	involves: C57BL/6NJcl * DBA/2NJcl	N	38786026
MGI:7643195	F	MP:0005389	reproductive system phenotype	Zar1l<em1Kzt>/Zar1l<em1Kzt>	involves: C57BL/6NJcl * DBA/2NJcl	N	38786026
MGI:7643207	M	MP:0005389	reproductive system phenotype	Acrv1<em1Osb>/Acrv1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	38697008
MGI:7643209	M	MP:0005389	reproductive system phenotype	Adgrf3<em1Kzt>/Adgrf3<em1Kzt>	involves: C57BL/6NJcl * DBA/2NJcl	N	38697008
MGI:7643210	M	MP:0005389	reproductive system phenotype	Atp8b5<em1Kzt>/Atp8b5<em1Kzt>	involves: C57BL/6NJcl * DBA/2NJcl	N	38697008
MGI:7643212	M	MP:0005389	reproductive system phenotype	Cfap276<em1Osb>/Cfap276<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38697008
MGI:7643213	M	MP:0005389	reproductive system phenotype	Cfap90<em1Osb>/Cfap90<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38697008
MGI:7643214	M	MP:0005389	reproductive system phenotype	Fbxw5<em1Osb>/Fbxw5<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38697008
MGI:7643216	M	MP:0001147	small testis	Gm17266<em1Osb>/Gm17266<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38697008
MGI:7643217	M	MP:0005389	reproductive system phenotype	Lrrd1<em1Osb>/Lrrd1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38697008
MGI:7643218	M	MP:0005389	reproductive system phenotype	Mroh7<em1Osb>/Mroh7<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38697008
MGI:7643219	M	MP:0005389	reproductive system phenotype	Nemp1<em1Osb>/Nemp1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38697008
MGI:7643220	M	MP:0005389	reproductive system phenotype	Spata45<em1Osb>/Spata45<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38697008
MGI:7643221	M	MP:0005389	reproductive system phenotype	Trim36<em1Osb>/Trim36<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38697008
MGI:7643226	M	MP:0005389	reproductive system phenotype	4933411K16Rik<em1Osb>/4933411K16Rik<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	Y	38835510
MGI:7643227	M	MP:0005389	reproductive system phenotype	BC048671<em1Osb>/BC048671<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38835510
MGI:7643228	M	MP:0005389	reproductive system phenotype	Cfap68<em1Osb>/Cfap68<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38835510
MGI:7643229	M	MP:0005389	reproductive system phenotype	Del(8Adam25-Adam39)1Kzt/Del(8Adam25-Adam39)1Kzt	involves: C57BL/6NJcl * DBA/2NJcl	N	38835510
MGI:7643230	M	MP:0005389	reproductive system phenotype	Gm13570<em1Kzt>/Gm13570<em1Kzt>	involves: C57BL/6NJcl * DBA/2NJcl	N	38835510
MGI:7643231	M	MP:0005389	reproductive system phenotype	Gm4846<em1Osb>/Gm4846<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38835510
MGI:7643232	M	MP:0005389	reproductive system phenotype	Gm4984<em1Osb>/Gm4984<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38835510
MGI:7643233	M	MP:0005389	reproductive system phenotype	Nt5c1b<em1Osb>/Nt5c1b<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38835510
MGI:7643234	M	MP:0005389	reproductive system phenotype	Ppp1r42<em1Osb>/Ppp1r42<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38835510
MGI:7643235	M	MP:0005389	reproductive system phenotype	Saxo4<em1Osb>/Saxo4<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38835510
MGI:7643236	M	MP:0005389	reproductive system phenotype	Sh3d21<em1Kzt>/Sh3d21<em1Kzt>	involves: C57BL/6NJcl * DBA/2NJcl	N	38835510
MGI:7643237	M	MP:0005389	reproductive system phenotype	Spz1<em1Osb>/Spz1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38835510
MGI:7643238	M	MP:0005389	reproductive system phenotype	Tektl1<em1Osb>/Tektl1<em1Osb>	involves: C57BL/6NJcl * DBA/2NJcl	N	38835510
MGI:7643813	M	MP:0010027	increased liver cholesterol level	Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2c70<em1Utr>	N	31645370
MGI:7643813	M	MP:0002941	increased circulating alanine transaminase level	Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2c70<em1Utr>	N	31645370
MGI:7643813	M	MP:0002968	increased circulating alkaline phosphatase level	Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2c70<em1Utr>	N	31645370
MGI:7643813	M	MP:0002928	abnormal bile duct morphology	Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2c70<em1Utr>	N	31645370
MGI:7643813	M	MP:0001654	hepatic necrosis	Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2c70<em1Utr>	N	31645370
MGI:7643813	M	MP:0000598	abnormal liver morphology	Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2c70<em1Utr>	N	31645370
MGI:7643813	M	MP:0005178	increased circulating cholesterol level	Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2c70<em1Utr>	N	31645370
MGI:7643813	M	MP:0002981	increased liver weight	Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2c70<em1Utr>	N	31645370
MGI:7643813	M	MP:0001860	liver inflammation	Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2c70<em1Utr>	N	31645370
MGI:7643815	M	MP:0004773	abnormal bile composition	Cyp2a12<em1Utr>/Cyp2a12<em1Utr>,Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2a12<em1Utr> Cyp2c70<em1Utr>	N	31645370
MGI:7643815	M	MP:0002968	increased circulating alkaline phosphatase level	Cyp2a12<em1Utr>/Cyp2a12<em1Utr>,Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2a12<em1Utr> Cyp2c70<em1Utr>	N	31645370
MGI:7643815	M	MP:0002941	increased circulating alanine transaminase level	Cyp2a12<em1Utr>/Cyp2a12<em1Utr>,Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2a12<em1Utr> Cyp2c70<em1Utr>	N	31645370
MGI:7643815	M	MP:0002928	abnormal bile duct morphology	Cyp2a12<em1Utr>/Cyp2a12<em1Utr>,Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2a12<em1Utr> Cyp2c70<em1Utr>	N	31645370
MGI:7643815	M	MP:0005179	decreased circulating cholesterol level	Cyp2a12<em1Utr>/Cyp2a12<em1Utr>,Cyp2c70<em1Utr>/Cyp2c70<em1Utr>	C57BL/6J-Cyp2a12<em1Utr> Cyp2c70<em1Utr>	N	31645370
MGI:7645413	M	MP:0006036	abnormal mitochondrial physiology	Gt(ROSA)26Sor<em1(Tbc1d15)Jren>/Gt(ROSA)26Sor<em1(Tbc1d15)Jren>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: C57BL/6N * FVB/N	N	35680100
MGI:7645413	M	MP:0031216	decreased susceptibility to myocardial ischemic injury	Gt(ROSA)26Sor<em1(Tbc1d15)Jren>/Gt(ROSA)26Sor<em1(Tbc1d15)Jren>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: C57BL/6N * FVB/N	N	35680100
MGI:7645413	M	MP:0003038	decreased myocardial infarct size	Gt(ROSA)26Sor<em1(Tbc1d15)Jren>/Gt(ROSA)26Sor<em1(Tbc1d15)Jren>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: C57BL/6N * FVB/N	N	35680100
MGI:7645414	M	MP:0031217	increased susceptibility to myocardial ischemic injury	Tbc1d15<em1Jren>/Tbc1d15<em1Jren>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: C57BL/6N * FVB/N	N	35680100
MGI:7645414	M	MP:0003037	increased myocardial infarct size	Tbc1d15<em1Jren>/Tbc1d15<em1Jren>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: C57BL/6N * FVB/N	N	35680100
MGI:7645414	M	MP:0006036	abnormal mitochondrial physiology	Tbc1d15<em1Jren>/Tbc1d15<em1Jren>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: C57BL/6N * FVB/N	N	35680100
MGI:7645414	M	MP:0014239	abnormal intracellular organelle morphology	Tbc1d15<em1Jren>/Tbc1d15<em1Jren>,A1cf<Tg(Myh6-cre/Esr1*)1Jmk>/A1cf<+>	involves: C57BL/6N * FVB/N	N	35680100
MGI:7645491	M	MP:0004499	increased incidence of tumors by chemical induction	Foxp3<tm4(YFP/icre)Ayr>/Y,Zfp91<tm1Smoc>/Zfp91<tm1Smoc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	33355624
MGI:7645491	M	MP:0008537	increased susceptibility to induced colitis	Foxp3<tm4(YFP/icre)Ayr>/Y,Zfp91<tm1Smoc>/Zfp91<tm1Smoc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	33355624
MGI:7645491	M	MP:0004946	abnormal regulatory T cell physiology	Foxp3<tm4(YFP/icre)Ayr>/Y,Zfp91<tm1Smoc>/Zfp91<tm1Smoc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	33355624
MGI:7645491	M	MP:0004974	decreased regulatory T cell number	Foxp3<tm4(YFP/icre)Ayr>/Y,Zfp91<tm1Smoc>/Zfp91<tm1Smoc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	33355624
MGI:7645491	M	MP:0008078	increased CD8-positive, alpha-beta T cell number	Foxp3<tm4(YFP/icre)Ayr>/Y,Zfp91<tm1Smoc>/Zfp91<tm1Smoc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	33355624
MGI:7645491	M	MP:0005350	increased susceptibility to autoimmune disorder	Foxp3<tm4(YFP/icre)Ayr>/Y,Zfp91<tm1Smoc>/Zfp91<tm1Smoc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	33355624
MGI:7645511	M	MP:0004946	abnormal regulatory T cell physiology	Becn1<tm1Smoc>/Becn1<tm1Smoc>,Foxp3<tm4(YFP/icre)Ayr>/0	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	33355624
MGI:7645512	M	MP:0004946	abnormal regulatory T cell physiology	Becn1<tm1Smoc>/Becn1<tm1Smoc>,Zfp91<tm1Smoc>/Zfp91<tm1Smoc>,Foxp3<tm4(YFP/icre)Ayr>/Y	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	N	33355624
MGI:7646888	M	MP:0009480	distended cecum	Hapstr1<tm1.1Menm>/Hapstr1<tm1.1Menm>,Tg(CAG-cre/Esr1*)5Amc/0	involves: C57BL/6 * C57BL/6J * CBA	N	38453366
MGI:7646977	F	MP:0002907	abnormal parturition	Dnmt3a<em1Hsas>/Dnmt3a<em1Hsas>	C57BL/6J-Dnmt3a<em1Hsas>	N	37527244
MGI:7646977	F	MP:0003787	abnormal imprinting	Dnmt3a<em1Hsas>/Dnmt3a<em1Hsas>	C57BL/6J-Dnmt3a<em1Hsas>	N	37527244
MGI:7646977	F	MP:0008878	abnormal DNA methylation during gametogenesis	Dnmt3a<em1Hsas>/Dnmt3a<em1Hsas>	C57BL/6J-Dnmt3a<em1Hsas>	N	37527244
MGI:7646977	F	MP:0009661	abnormal pregnancy	Dnmt3a<em1Hsas>/Dnmt3a<em1Hsas>	C57BL/6J-Dnmt3a<em1Hsas>	N	37527244
MGI:7646977	F	MP:0003787	abnormal imprinting	Dnmt3a<em1Hsas>/Dnmt3a<em1Hsas>	C57BL/6J-Dnmt3a<em1Hsas>	N	38627502
MGI:7647010	M	MP:0006380	abnormal spermatid morphology	Dnmt3a<em1Hsas>/Dnmt3a<em1Hsas>,Dnmt3l<em1Hsas>/Dnmt3l<em1Hsas>	C57BL/6J-Dnmt3a<em1Hsas> Dnmt3l<em1Hsas>	N	38627502
MGI:7647010	M	MP:0002216	abnormal seminiferous tubule morphology	Dnmt3a<em1Hsas>/Dnmt3a<em1Hsas>,Dnmt3l<em1Hsas>/Dnmt3l<em1Hsas>	C57BL/6J-Dnmt3a<em1Hsas> Dnmt3l<em1Hsas>	N	38627502
MGI:7647010	M	MP:0009203	external male genitalia hypoplasia	Dnmt3a<em1Hsas>/Dnmt3a<em1Hsas>,Dnmt3l<em1Hsas>/Dnmt3l<em1Hsas>	C57BL/6J-Dnmt3a<em1Hsas> Dnmt3l<em1Hsas>	N	38627502
MGI:7647010	M	MP:0005578	teratozoospermia	Dnmt3a<em1Hsas>/Dnmt3a<em1Hsas>,Dnmt3l<em1Hsas>/Dnmt3l<em1Hsas>	C57BL/6J-Dnmt3a<em1Hsas> Dnmt3l<em1Hsas>	N	38627502
MGI:7647010	F	MP:0003787	abnormal imprinting	Dnmt3a<em1Hsas>/Dnmt3a<em1Hsas>,Dnmt3l<em1Hsas>/Dnmt3l<em1Hsas>	C57BL/6J-Dnmt3a<em1Hsas> Dnmt3l<em1Hsas>	N	38627502
MGI:7647010	F	MP:0005389	reproductive system phenotype	Dnmt3a<em1Hsas>/Dnmt3a<em1Hsas>,Dnmt3l<em1Hsas>/Dnmt3l<em1Hsas>	C57BL/6J-Dnmt3a<em1Hsas> Dnmt3l<em1Hsas>	Y	38627502
MGI:7647012	F	MP:0003787	abnormal imprinting	Dnmt3l<em1Hsas>/Dnmt3l<em1Hsas>	C57BL/6J-Dnmt3l<em1Hsas>	N	38627502
MGI:7647195	M	MP:0009230	abnormal sperm head morphology	Fsip1<em1Nali>/Fsip1<em1Nali>	C57BL/6J-Fsip1<em1Nali>	N	33901807
MGI:7647195	M	MP:0006380	abnormal spermatid morphology	Fsip1<em1Nali>/Fsip1<em1Nali>	C57BL/6J-Fsip1<em1Nali>	N	33901807
MGI:7647195	M	MP:0002686	globozoospermia	Fsip1<em1Nali>/Fsip1<em1Nali>	C57BL/6J-Fsip1<em1Nali>	N	33901807
MGI:7647195	M	MP:0002687	oligozoospermia	Fsip1<em1Nali>/Fsip1<em1Nali>	C57BL/6J-Fsip1<em1Nali>	N	33901807
MGI:7647195	M	MP:0001932	abnormal spermiogenesis	Fsip1<em1Nali>/Fsip1<em1Nali>	C57BL/6J-Fsip1<em1Nali>	N	33901807
MGI:7647195	M	MP:0009831	abnormal sperm midpiece morphology	Fsip1<em1Nali>/Fsip1<em1Nali>	C57BL/6J-Fsip1<em1Nali>	N	33901807
MGI:7647195	M	MP:0020451	decreased sperm progressive motility	Fsip1<em1Nali>/Fsip1<em1Nali>	C57BL/6J-Fsip1<em1Nali>	N	33901807
MGI:7647195	M	MP:0008892	abnormal sperm flagellum morphology	Fsip1<em1Nali>/Fsip1<em1Nali>	C57BL/6J-Fsip1<em1Nali>	N	33901807
MGI:7647195	M	MP:0005578	teratozoospermia	Fsip1<em1Nali>/Fsip1<em1Nali>	C57BL/6J-Fsip1<em1Nali>	N	33901807
MGI:7647229	M	MP:0008872	abnormal physiological response to xenobiotic	Mir379<em1Rnat>/Mir379<em1Rnat>	C57BL/6J-Mir379<em1Rnat>	N	33398021
MGI:7647260	F	MP:0010053	decreased grip strength	Ar<tm2Ska>/Ar<tm2Ska>,Tg(ACTA1-cre)79Jme/0	involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj * SJL	N	33870126
MGI:7647262	F	MP:0005369	muscle phenotype	Ar<tm2Ska>/Ar<tm2Ska>,Pax7<tm2.1(cre/ERT2)Fan>/Pax7<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrl	Y	33870126
MGI:7657422	M	MP:0010182	decreased susceptibility to weight gain	Ifrd1<tm1Lah>/Ifrd1<tm1Lah>,Ifrd2<tm1.1Lah>/Ifrd2<tm1.1Lah>	involves: 129 * 129P2/OlaHsd * C57BL/6J	N	37603466
MGI:7657422	M	MP:0008853	decreased abdominal adipose tissue amount	Ifrd1<tm1Lah>/Ifrd1<tm1Lah>,Ifrd2<tm1.1Lah>/Ifrd2<tm1.1Lah>	involves: 129 * 129P2/OlaHsd * C57BL/6J	N	37603466
MGI:7657422	M	MP:0011169	abnormal white fat cell differentation	Ifrd1<tm1Lah>/Ifrd1<tm1Lah>,Ifrd2<tm1.1Lah>/Ifrd2<tm1.1Lah>	involves: 129 * 129P2/OlaHsd * C57BL/6J	N	37603466
MGI:7657422	M	MP:0003960	increased lean body mass	Ifrd1<tm1Lah>/Ifrd1<tm1Lah>,Ifrd2<tm1.1Lah>/Ifrd2<tm1.1Lah>	involves: 129 * 129P2/OlaHsd * C57BL/6J	N	37603466
MGI:7657422	M	MP:0010025	decreased total body fat amount	Ifrd1<tm1Lah>/Ifrd1<tm1Lah>,Ifrd2<tm1.1Lah>/Ifrd2<tm1.1Lah>	involves: 129 * 129P2/OlaHsd * C57BL/6J	N	37603466
MGI:7657422	M	MP:0003868	abnormal feces composition	Ifrd1<tm1Lah>/Ifrd1<tm1Lah>,Ifrd2<tm1.1Lah>/Ifrd2<tm1.1Lah>	involves: 129 * 129P2/OlaHsd * C57BL/6J	N	37603466
MGI:7657425	M	MP:0001262	decreased body weight	Ifrd2<tm1.1Lah>/Ifrd2<tm1.1Lah>	B6.129-Ifrd2<tm1.1Lah>	N	37603466
MGI:7657425	M	MP:0008853	decreased abdominal adipose tissue amount	Ifrd2<tm1.1Lah>/Ifrd2<tm1.1Lah>	B6.129-Ifrd2<tm1.1Lah>	N	37603466
MGI:7657425	M	MP:0010025	decreased total body fat amount	Ifrd2<tm1.1Lah>/Ifrd2<tm1.1Lah>	B6.129-Ifrd2<tm1.1Lah>	N	37603466
MGI:7657425	M	MP:0011169	abnormal white fat cell differentation	Ifrd2<tm1.1Lah>/Ifrd2<tm1.1Lah>	B6.129-Ifrd2<tm1.1Lah>	N	37603466
MGI:7657546	M	MP:0010723	paternal effect	Trim66<em1Emr>/Trim66<em1Emr>	FVB/NCrl-Trim66<em1Emr>	N	38719749
MGI:7657546	M	MP:0005389	reproductive system phenotype	Trim66<em1Emr>/Trim66<em1Emr>	FVB/NCrl-Trim66<em1Emr>	Y	38719749
MGI:7657548	M	MP:0010723	paternal effect	Trim66<em2Emr>/Trim66<em2Emr>	C57BL/6JCrl-Trim66<em2Emr>	N	38719749
MGI:7657548	M	MP:0005389	reproductive system phenotype	Trim66<em2Emr>/Trim66<em2Emr>	C57BL/6JCrl-Trim66<em2Emr>	Y	38719749
MGI:7659107	M	MP:0001262	decreased body weight	Ctps1<tm1c(KOMP)Wtsi>/Ctps1<tm1c(KOMP)Wtsi>,Tg(Cd4-cre)1Cwi/0,Foxp3<sf>/Y,Rag1<tm1Mom>/Rag1<+>	mixed	N	38438357
MGI:7659107	M	MP:0005095	decreased T cell proliferation	Ctps1<tm1c(KOMP)Wtsi>/Ctps1<tm1c(KOMP)Wtsi>,Tg(Cd4-cre)1Cwi/0,Foxp3<sf>/Y,Rag1<tm1Mom>/Rag1<+>	mixed	N	38438357
MGI:7659107	M	MP:0001876	decreased inflammatory response	Ctps1<tm1c(KOMP)Wtsi>/Ctps1<tm1c(KOMP)Wtsi>,Tg(Cd4-cre)1Cwi/0,Foxp3<sf>/Y,Rag1<tm1Mom>/Rag1<+>	mixed	N	38438357
MGI:7659107	M	MP:0004974	decreased regulatory T cell number	Ctps1<tm1c(KOMP)Wtsi>/Ctps1<tm1c(KOMP)Wtsi>,Tg(Cd4-cre)1Cwi/0,Foxp3<sf>/Y,Rag1<tm1Mom>/Rag1<+>	mixed	N	38438357
MGI:7659107	M	MP:0000691	enlarged spleen	Ctps1<tm1c(KOMP)Wtsi>/Ctps1<tm1c(KOMP)Wtsi>,Tg(Cd4-cre)1Cwi/0,Foxp3<sf>/Y,Rag1<tm1Mom>/Rag1<+>	mixed	N	38438357
MGI:7659213	F	MP:0000063	decreased bone mineral density	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0020040	decreased bone ossification	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0005331	insulin resistance	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0005293	impaired glucose tolerance	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0005669	increased circulating leptin level	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0000130	abnormal trabecular bone morphology	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0005378	growth/size/body region phenotype	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	Y	36424386
MGI:7659213	F	MP:0009117	abnormal white fat cell morphology	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0009130	increased white fat cell number	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0011711	impaired osteoblast differentiation	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0000008	increased white adipose tissue amount	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0030009	increased bone marrow adipose tissue amount	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0011168	abnormal fat cell differentiation	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0011720	abnormal ossification involved in bone remodeling	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0001926	female infertility	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0006094	increased fat cell size	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0000137	abnormal vertebrae morphology	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0020010	decreased bone mineral density of femur	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0004016	decreased bone mass	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0003797	abnormal compact bone morphology	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0004893	decreased adiponectin level	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659213	F	MP:0021186	decreased bone mineral density of vertebrae	Il11<tm1Moto>/Il11<tm1Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7659219	F	MP:0001926	female infertility	Il11<tm2Moto>/Il11<tm2Moto>	involves: C57BL/6NCrlj * CBA/JNCrlj	N	36424386
MGI:7660516	M	MP:0011350	abnormal proximal convoluted tubule brush border morphology	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660516	M	MP:0020404	prolinuria	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660516	M	MP:0003311	aminoaciduria	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660516	M	MP:0002871	albuminuria	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660516	M	MP:0008260	abnormal autophagy	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660516	M	MP:0010107	abnormal renal reabsorption	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660516	M	MP:0020400	cystinuria	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660516	M	MP:0005619	increased urine potassium level	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660516	M	MP:0004756	abnormal proximal convoluted tubule morphology	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660516	M	MP:0030939	abnormal autophagosome formation	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660516	M	MP:0002901	increased urine phosphate level	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660516	M	MP:0001759	increased urine glucose level	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660516	M	MP:0020849	abnormal actin cytoskeleton morphology	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660516	M	MP:0030617	hyperglutaminuria	Whamm<tm1b(KOMP)Wtsi>/Whamm<tm1b(KOMP)Wtsi>	B6N(Cg)-Whamm<tm1b(KOMP)Wtsi>/3J	N	38598293
MGI:7660971	F	MP:0014221	increased colon goblet cell number	Btbd8<em1Lych>/Btbd8<em1Lych>	involves: C57BL/6	N	38558797
MGI:7660971	F	MP:0014201	abnormal intestinal epithelium physiology	Btbd8<em1Lych>/Btbd8<em1Lych>	involves: C57BL/6	N	38558797
MGI:7660971	F	MP:0008539	decreased susceptibility to induced colitis	Btbd8<em1Lych>/Btbd8<em1Lych>	involves: C57BL/6	N	38558797
MGI:7660971	F	MP:0008874	decreased physiological sensitivity to xenobiotic	Btbd8<em1Lych>/Btbd8<em1Lych>	involves: C57BL/6	N	38558797
MGI:7660971	F	MP:0010155	abnormal intestine physiology	Btbd8<em1Lych>/Btbd8<em1Lych>	involves: C57BL/6	N	38558797
MGI:7660971	F	MP:0008882	abnormal enterocyte physiology	Btbd8<em1Lych>/Btbd8<em1Lych>	involves: C57BL/6	N	38558797
MGI:7660971	F	MP:0011079	decreased macrophage cytokine production	Btbd8<em1Lych>/Btbd8<em1Lych>	involves: C57BL/6	N	38558797
